Sample records for freely dissolved concentration

  1. Effects of dissolved organic matter from a eutrophic lake on the freely dissolved concentrations of emerging organic contaminants.

    PubMed

    Xiao, Yi-Hua; Huang, Qing-Hui; Vähätalo, Anssi V; Li, Fei-Peng; Chen, Ling

    2014-08-01

    The authors studied the effects of dissolved organic matter (DOM) on the bioavailability of bisphenol A (BPA) and chloramphenicol by measuring the freely dissolved concentrations of the contaminants in solutions containing DOM that had been isolated from a mesocosm in a eutrophic lake. The abundance and aromaticity of the chromophoric DOM increased over the 25-d mesocosm experiment. The BPA freely dissolved concentration was 72.3% lower and the chloramphenicol freely dissolved concentration was 56.2% lower using DOM collected on day 25 than using DOM collected on day 1 of the mesocosm experiment. The freely dissolved concentrations negatively correlated with the ultraviolent absorption coefficient at 254 nm and positively correlated with the spectral slope of chromophoric DOM, suggesting that the bioavailability of these emerging organic contaminants depends on the characteristics of the DOM present. The DOM-water partition coefficients (log KOC ) for the emerging organic contaminants positively correlated with the aromaticity of the DOM, measured as humic acid-like fluorescent components C1 (excitation/emission=250[313]/412 nm) and C2 (excitation/emission=268[379]/456 nm). The authors conclude that the bioavailability of emerging organic contaminants in eutrophic lakes can be affected by changes in the DOM. © 2014 SETAC.

  2. Distribution of polycyclic aromatic hydrocarbons in southern Chesapeake Bay surface water: Evaluation of three methods for determining freely dissolved water concentrations

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Gustafson, K.E.; Dickhut, R.M.

    1997-03-01

    Gas sparging, semipermeable-membrane devices (SPMDs), and filtration with sorption of dissolved polycyclic aromatic hydrocarbons (PAHs) to XAD-2 resin were evaluated for determining the concentrations of freely dissolved PAHs in estuarine waters of southern Chesapeake Bay at sites ranging from rural to urban and highly industrialized. Gas sparging had significant sampling artifacts due to particle scavenging by rising bubbles, and SPMDs were kinetically limited for four-ring and larger PAHs relative to short-term temporal changes in water concentrations. Filtration with sorption of the dissolved contaminant fraction to XAD-2 resin was found to be the most accurate and feasible method for determining concentrationsmore » of freely dissolved PAHs in estuarine water. Concentrations and distribution coefficients of dissolved and particulate PAHs were measured using the filtration/XAD-2 method. Concentrations of PAHs in surface waters of southern Chesapeake Bay were higher than those reported for the northern bay; concentrations in the Elizabeth River were elevated relative to all other sites. A gradient for particulate PAHs was observed from urban to remote sites. No seasonal trends were observed in dissolved or particle-bound PAH fractions at any site. Distributions of dissolved and particulate PAHs in surface waters of the Chesapeake Bay are near equilibrium at all locations and during all seasons.« less

  3. Passive sampling methods for contaminated sediments: Scientific rationale supporting use of freely dissolved concentrations

    PubMed Central

    Mayer, Philipp; Parkerton, Thomas F; Adams, Rachel G; Cargill, John G; Gan, Jay; Gouin, Todd; Gschwend, Philip M; Hawthorne, Steven B; Helm, Paul; Witt, Gesine; You, Jing; Escher, Beate I

    2014-01-01

    Passive sampling methods (PSMs) allow the quantification of the freely dissolved concentration (Cfree) of an organic contaminant even in complex matrices such as sediments. Cfree is directly related to a contaminant's chemical activity, which drives spontaneous processes including diffusive uptake into benthic organisms and exchange with the overlying water column. Consequently, Cfree provides a more relevant dose metric than total sediment concentration. Recent developments in PSMs have significantly improved our ability to reliably measure even very low levels of Cfree. Application of PSMs in sediments is preferably conducted in the equilibrium regime, where freely dissolved concentrations in the sediment are well-linked to the measured concentration in the sampler via analyte-specific partition ratios. The equilibrium condition can then be assured by measuring a time series or a single time point using passive samplers with different surface to volume ratios. Sampling in the kinetic regime is also possible and generally involves the application of performance reference compounds for the calibration. Based on previous research on hydrophobic organic contaminants, it is concluded that Cfree allows a direct assessment of 1) contaminant exchange and equilibrium status between sediment and overlying water, 2) benthic bioaccumulation, and 3) potential toxicity to benthic organisms. Thus, the use of PSMs to measure Cfree provides an improved basis for the mechanistic understanding of fate and transport processes in sediments and has the potential to significantly improve risk assessment and management of contaminated sediments. Integr Environ Assess Manag 2014;10:197–209. © 2014 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals, Inc. on behalf of SETAC. PMID:24288295

  4. Ion exchange membranes as novel passive sampling material for organic ions: application for the determination of freely dissolved concentrations.

    PubMed

    Oemisch, Luise; Goss, Kai-Uwe; Endo, Satoshi

    2014-11-28

    Many studies in pharmacology, toxicology and environmental science require a method for determining the freely dissolved concentration of a target substance. A recently developed tool for this purpose is equilibrium passive sampling with polymeric materials. However, this method has rarely been applied to ionic organic substances, primarily due to limited availability of convenient sorption materials. This study introduces ion exchange membranes (IEMs) as a novel passive sampling material for organic ions. The partitioning of 4-ethylbenzene-1-sulfonate, 2,4-dichlorophenoxyacetic acid and pentachlorophenol to one anion exchange membrane (FAS) and of difenzoquat, nicotine and verapamil to one cation exchange membrane (FKS) was investigated. All test substances exhibited a sufficiently high affinity for the respective IEM with logarithmic IEM-water partition coefficients >2.3. Sorption equilibrium was established quickly, within several hours for the FAS membrane and within 1-3 days for the FKS membrane. For permanently charged substances the partitioning to the IEMs was independent of pH, but was influenced by the salt composition of the test solution. For all test substances sorption to IEM was dependent on the substance concentration. Bovine serum albumin-water partition coefficients determined by passive sampling with IEMs agree well with those determined by the conventional dialysis method. The results of this study indicate that IEMs exhibit the potential to measure freely dissolved concentrations of organic ions in a simple and time-saving manner. Copyright © 2014 Elsevier B.V. All rights reserved.

  5. Validity of using semipermeable membrane devices for determining aqueous concentrations of freely dissolved PAHs

    USGS Publications Warehouse

    Prest, Harry; Petty, J.D.; Huckins, J.N.

    1998-01-01

    An in-depth review of the recent contribution to this journal by Gustafson and Dickhut [1] prompts us to share our concerns regarding some of their conclusions. The paper presents data comparing three techniques for determining aqueous concentrations of freely dissolved polycyclic aromatic hydrocarbons (PAHs) gas sparging, lipid-containing semipermeable membrane devices (SPMDs) of the U.S. Geological Survey (USGS) design, and filtration followed by sorption using XAD-2 resin. Space limitations force us to limit our comments to problems resulting from an apparent lack of understanding of how SPMDs function. Several recent publications [2–13] have described the theoretical and practical considerations of SPMD usage. Gustafson and Dickhut fail to cite any papers describing SPMDs published after 1992, even though some 18 papers have been published in American and European journals since then and several SPMD studies have been presented at many major meetings.

  6. Performance of passive sampling with low-density polyethylene membranes for the estimation of freely dissolved DDx concentrations in lake environments.

    PubMed

    Borrelli, Raffaella; Tcaciuc, A Patricia; Verginelli, Iason; Baciocchi, Renato; Guzzella, Licia; Cesti, Pietro; Zaninetta, Luciano; Gschwend, Philip M

    2018-06-01

    Laboratory and field studies were used to evaluate the performance of low-density polyethylene (PE) passive samplers for assessing the freely dissolved concentrations of DDT and its degradates (DDD and DDE, together referred to as DDx) in an Italian lake environment. We tested commercially available 25 μm thick PE sheets as well as specially synthesized, 10 μm thick PE films which equilibrated with their surroundings more quickly. We measured PE-water partitioning coefficients (K pew ) of the 10 μm thick PE films, finding good correspondence with previously reported values for thicker PE. Use of the 10 μm PE for ex situ sampling of a lake sediment containing DDx in laboratory tumbling experiments showed repeatability of ±15% (= standard deviation/mean). Next, we deployed replicate 10 μm and 25 μm PE samplers (N = 4 for 10 d and for 30 d) in the water and sediment of a lake located in northern Italy; the results showed dissolved DDx concentrations in the picogram/L range in porewater and the bottom water. Values deduced from 10 μm thick PE films compared well (95% of all comparison pairs matched within a factor of 5) with those obtained using PE films of 25 μm thickness when dissolved DDx concentrations were estimated using performance reference compound (PRC) corrections, whether left at the bed-water interface for 10 or 30 days. These results demonstrated the potential of this sampling method to provide estimation of the truly dissolved DDx concentrations, and thereby the mobile and bio-available fractions in both surface waters and sediment beds. Copyright © 2018 Elsevier Ltd. All rights reserved.

  7. Addition of biochar to sewage sludge decreases freely dissolved PAHs content and toxicity of sewage sludge-amended soil.

    PubMed

    Stefaniuk, Magdalena; Oleszczuk, Patryk

    2016-11-01

    Due to an increased content of polycyclic aromatic hydrocarbons (PAHs) frequently found in sewage sludges, it is necessary to find solutions that will reduce the environmental hazard associated with their presence. The aim of this study was to determine changes of total and freely dissolved concentration of PAHs in sewage sludge-biochar-amended soil. Two different sewage sludges and biochars with varying properties were tested. Biochars (BC) were produced from biogas residues at 400 °C or 600 °C and from willow at 600 °C. The freely dissolved PAH concentration was determined by means of passive sampling using polyoxymethylene (POM). Total and freely dissolved PAH concentration was monitored at the beginning of the experiment and after 90 days of aging of the sewage sludge with the biochar and soil. Apart from chemical evaluation, the effect of biochar addition on the toxicity of the tested materials on bacteria - Vibrio fischeri (Microtox ® ), plants - Lepidium sativum (Phytotestkit F, Phytotoxkit F), and Collembola - Folsomia candida (Collembolan test) was evaluated. The addition of biochar to the sewage sludges decreased the content of C free PAHs. A reduction from 11 to 43% of sewage sludge toxicity or positive effects on plants expressed by root growth stimulation from 6 to 25% to the control was also found. The range of reduction of C free PAHs and toxicity was dependent on the type of biochar. After 90 days of incubation of the biochars with the sewage sludge in the soil, C free PAHs and toxicity were found to further decrease compared to the soil with sewage sludge alone. The obtained results show that the addition of biochar to sewage sludges may significantly reduce the risk associated with their environmental use both in terms of PAH content and toxicity of the materials tested. Copyright © 2016 Elsevier Ltd. All rights reserved.

  8. Measuring freely dissolved water concentrations of PCBs using LDPE passive samplers and performance reference compounds (PRCs)

    EPA Science Inventory

    Low-Density polyethylene (LDPE) sheets are often used as passive samplers for aquatic environmental monitoring to measure the dissolved concentrations of hydrophobic organic contaminants (HOCs). These concentrations are then used to evaluate the potential for ecological and human...

  9. Effect of pyrolysis temperatures on freely dissolved polycyclic aromatic hydrocarbon (PAH) concentrations in sewage sludge-derived biochars.

    PubMed

    Zielińska, Anna; Oleszczuk, Patryk

    2016-06-01

    The aim of this study was to evaluate the effect of sewage sludge pyrolysis on freely dissolved (Cfree) polycyclic aromatic hydrocarbon (PAH) contents in biochars. Four sewage sludges with varying properties and PAH contents were pyrolysed at temperatures of 500 °C, 600 °C or 700 °C. Cfree PAH contents were determined using polyoxymethylene (POM). The contents of Cfree PAHs in the sludges ranged from 262 to 294 ng L(-1). Sewage sludge-derived biochars have from 2.3- to 3.4-times lower Cfree PAH contents comparing to corresponding sewage sludges. The Cfree PAH contents in the biochars ranged between 81 ng L(-1) and 126 ng L(-1). As regards agricultural use of biochar, the lower contents of Cfree PAHs in the biochars compared to the sewage sludges makes biochar a safer material than sewage sludge in terms of PAH contents. Copyright © 2016 Elsevier Ltd. All rights reserved.

  10. Polyoxymethylene passive samplers to assess the effectiveness of biochar by reducing the content of freely dissolved fipronil and ethiprole.

    PubMed

    Li, Shasha; Wang, Pingping; Liu, Xingang; Wu, Xiaohu; Dong, Fengshou; Xu, Jun; Zheng, Yongquan

    2018-07-15

    An equilibrium passive sampler based on polyoxymethylene (POM) was used to determine the freely dissolved concentrations (C free ) of fipronil and ethiprole. The sorption equilibrium times of fipronil and ethiprole in POM were 14.2d and 24.0d, respectively. The POM-water partitioning coefficients (logK POM-water ) were 2.6 for fipronil and 1.4 for ethiprole. The method was further used to evaluate the sorption behavior of biochars which produced by pyrolysis of Magnolia wood (Magnolia denudata) at 300°C, 500°C and 700°C. The amounts of target compounds adsorbed increased with increasing pyrolysis temperature of the biochars. Biochars characterized by a low polarity index had better sorption capacity for the target compounds. The additions of biochars to sediment were effective in reducing C free , and the enhancement was found to be more pronounced with high biochar content. C free in sediment with more organic matter was significantly higher after biochar addition. Increasing the sediment-biochar contact time from 7 to 30d resulted in an increase in sorption of the compounds. We conclude that Magnolia wood biochar effectively reduces the content of freely dissolved fipronil and ethiprole content in sediment. Copyright © 2018. Published by Elsevier B.V.

  11. Spatial and temporal variation of freely dissolved PAHs in an urban river undergoing Superfund remediation

    PubMed Central

    Sower, GJ; Anderson, K.A.

    2014-01-01

    Urban rivers with a history of industrial use can exhibit spatial and temporal variations in contaminant concentrations that may significantly affect risk evaluations and even the assessment of remediation efforts. Concentrations of 15 biologically available priority pollutant polycyclic aromatic hydrocarbons (PAHs) were measured over five years along 18.5 miles of the lower Willamette River using passive sampling devices and HPLC. The study area includes the Portland Harbor Superfund megasite with several PAH sources including remediation operations for coal tar at RM 6.3 west and an additional Superfund site, McCormick and Baxter, at RM 7 east consisting largely of creosote contamination. Study results show that organoclay capping at the McCormick and Baxter Superfund Site reduced PAHs from a pre-cap average of 440 ± 422 ng/L to 8 ± 3 ng/L post-capping. Results also reveal that dredging of submerged coal tar nearly tripled nearby freely dissolved PAH concentrations. For apportioning sources, fluoranthene/ pyrene and phenanthrene/anthracene diagnostic ratios from passive sampling devices were established for creosote and coal tar contamination and compared to published sediment values. PMID:19174872

  12. Application of passive sampling for measuring dissolved concentrations of organic contaminants in the water column at three marine superfund sites

    EPA Science Inventory

    At contaminated sediment sites, including U.S. EPA Superfund sites, it is critical to measure water column concentrations of freely dissolved contaminants to understand the complete exposure of aquatic organisms to hydrophobic organic contaminants (HOCs). However, historically a...

  13. Spatial and temporal variation of freely dissolved polycyclic aromatic hydrocarbons in an urban river undergoing Superfund remediation.

    PubMed

    Sower, Gregory James; Anderson, Kim A

    2008-12-15

    Urban rivers with a history of industrial use can exhibit spatial and temporal variations in contaminant concentrations that may significantly affect risk evaluations and even the assessment of remediation efforts. Concentrations of 15 biologically available priority pollutant polycyclic aromatic hydrocarbons (PAHs) were measured over five years along 18.5 miles of the lower Willamette River using passive sampling devices and HPLC. The study area includes the Portland Harbor Superfund megasite with several PAH sources including remediation operations for coal tar at RM 6.3 west and an additional Superfund site, McCormick and Baxter, at RM 7 east consisting largely of creosote contamination. Study results show that organoclay capping at the McCormick and Baxter Superfund Site reduced PAHs from a precap average of 440 +/- 422 ng/L to 8 +/- 3 ng/L postcapping. Results also reveal that dredging of submerged coal tar nearly tripled nearby freely dissolved PAH concentrations. For apportioning sources, fluoranthene/pyrene and phenanthrene/anthracene diagnostic ratios from passive sampling devices were established for creosote and coal tar contamination and compared to published sediment values.

  14. Spatial and temporal variation of freely dissolved polycyclic aromatic hydrocarbons in an urban river undergoing Superfund remediation

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Aregory James Sower; Kim A. Anderson

    2008-12-15

    Urban rivers with a history of industrial use can exhibit spatial and temporal variations in contaminant concentrations that may significantly affect risk evaluations and even the assessment of remediation efforts. Concentrations of 15 biologically available priority pollutant polycyclic aromatic hydrocarbons (PAHs) were measured over five years along 18.5 miles of the lower Willamette River using passive sampling devices and HPLC. The study area includes the Portland Harbor Superfund megasite with several PAH sources including remediation operations for coal tar at RM 6.3 west and an additional Superfund site, McCormick and Baxter, at RM 7 east consisting largely of creosote contamination.more » Study results show that organoclay capping at the McCormick and Baxter Superfund Site reduced PAHs from a precap average of 440 {+-} 422 ng/L to 8 {+-} 3 ng/L postcapping. Results also reveal that dredging of submerged coal tar nearly tripled nearby freely dissolved PAH concentrations. For apportioning sources, fluoranthene/pyrene and phenanthrene/anthracene diagnostic ratios from passive sampling devices were established for creosote and coal tar contamination and compared to published sediment values. 29 refs., 3 figs., 3 tabs.« less

  15. Application of Passive Sampling for Measuring Dissolved Concentrations of Organic Contaminants in the Water Column at Three U.S. EPA Marine Superfund Sites

    EPA Science Inventory

    At contaminated sediment sites, including U.S. EPA Superfund sites, it is critical to measure water column concentrations of freely dissolved contaminants to understand the complete exposure of aquatic organisms to hydrophobic organic contaminants (HOCs). Historically acquiring ...

  16. Application of Passive Sampling for Measuring Dissolved Concentrations of Organic Contaminants in the Water Column at Three U.S. EPA Marine Superfund Sites.

    EPA Science Inventory

    At contaminated sediment sites, including U.S. EPA Superfund sites, it is critical to measure water column concentrations of freely dissolved contaminants to understand the complete exposure of aquatic organisms to hydrophobic organic contaminants (HOCs). Historically, acquiring...

  17. The concentration and changes in freely dissolved polycyclic aromatic hydrocarbons in biochar-amended soil.

    PubMed

    Oleszczuk, Patryk; Kuśmierz, Marcin; Godlewska, Paulina; Kraska, Piotr; Pałys, Edward

    2016-07-01

    The presence of polycyclic aromatic hydrocarbons (PAHs) in biochars hinders their environmental use. The aim of this study was to determine the freely dissolved (Cfree) PAH content in soil amended with biochar in a long-term (851 days) field experiment. Biochar was added to the soil at a rate of 30 and 45 t/ha. The addition of biochar to the soil resulted in a decrease in Σ13 Cfree PAHs by 25 and 22%, in the soil with the addition of biochar at the rate of 30 and 45 t/ha, respectively. As far as individual PAHs are concerned, in most cases a reduction in Cfree was also observed (from 3.6 to 66%, depending on the biochar rate). During the first 105 days of the experiment, the content of Σ13 Cfree in the biochar-amended soil significantly decreased by 26% (30 t/ha) and 36% (45 t/ha). After this period of time until the end of the experiment, no significant changes in Cfree were observed, regardless of the biochar rate. However, the behavior of individual PAH groups differed depending on the number of rings and experimental treatment. Ultimately, after 851 days of the experiment the content of Σ13 Cfree PAHs was lower by 29% (30 t/ha) and 35% (45 t/ha) compared to the beginning of the study as well as lower by 40% (30 t/ha) and 42% (45 t/ha) than in the control soil. The log KTOC coefficients calculated for the biochar-amended soils were higher immediately after adding biochar and subsequently they gradually decreased, indicating the reduced strength of the interaction between biochar and the studied PAHs. The obtained results show that the addition of biochar to soil does not create a risk in terms of the content of Cfree PAHs. Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. Gaseous and Freely-Dissolved PCBs in the Lower Great Lakes Based on Passive Sampling: Spatial Trends and Air-Water Exchange.

    PubMed

    Liu, Ying; Wang, Siyao; McDonough, Carrie A; Khairy, Mohammed; Muir, Derek C G; Helm, Paul A; Lohmann, Rainer

    2016-05-17

    Polyethylene passive sampling was performed to quantify gaseous and freely dissolved polychlorinated biphenyls (PCBs) in the air and water of Lakes Erie and Ontario during 2011-2012. In view of differing physical characteristics and the impacts of historical contamination by PCBs within these lakes, spatial variation of PCB concentrations and air-water exchange across these lakes may be expected. Both lakes displayed statistically similar aqueous and atmospheric PCB concentrations. Total aqueous concentrations of 29 PCBs ranged from 1.5 pg L(-1) in the open lake of Lake Erie (site E02) in 2011 spring to 105 pg L(-1) in Niagara (site On05) in 2012 summer, while total atmospheric concentrations were 7.7-634 pg m(-3) across both lakes. A west-to-east gradient was observed for aqueous PCBs in Lake Erie. River discharge and localized influences (e.g., sediment resuspension and regional alongshore transport) likely dominated spatial trends of aqueous PCBs in both lakes. Air-water exchange fluxes of Σ7PCBs ranged from -2.4 (±1.9) ng m(-2) day(-1) (deposition) in Sheffield (site E03) to 9.0 (±3.1) ng m(-2) day(-1) (volatilization) in Niagara (site On05). Net volatilization of PCBs was the primary trend across most sites and periods. Almost half of variation in air-water exchange fluxes was attributed to the difference in aqueous concentrations of PCBs. Uncertainty analysis in fugacity ratios and mass fluxes in air-water exchange of PCBs indicated that PCBs have reached or approached equilibrium only at the eastern Lake Erie and along the Canadian shore of Lake Ontario sites, where air-water exchange fluxes dominated atmospheric concentrations.

  19. Effect of membrane filtration artifacts on dissolved trace element concentrations

    USGS Publications Warehouse

    Horowitz, Arthur J.; Elrick, Kent A.; Colberg, Mark R.

    1992-01-01

    Among environment scientists, the current and almost universally accepted definition of dissolved constituents is an operational one; only those materials which pass through a 0.45-??m membrane filter are considered to be dissolved. Detailed laboratory and field studies on Fe and Al indicate that a number of factors associated with filtration, other than just pore size, can substantially alter 'dissolved' trace element concentrations; these include: filter type, filter diameter, filtration method, volume of sample processed, suspended sediment concentration, suspended sediment grain-size distribution, concentration of colloids and colloidally associated trace elements and concentration of organic matter. As such, reported filtered-water concentrations employing the same pore size filter may not be equal. Filtration artifacts may lead to the production of chemical data that indicate seasonal or annual 'dissolved' chemical trends which do not reflect actual environmental conditions. Further, the development of worldwide averages for various dissolved chemical constituents, the quantification of geochemical cycles, and the determination of short- or long-term environmental chemical trends may be subject to substantial errors, due to filtration artifacts, when data from the same or multiple sources are combined. Finally, filtration effects could have a substantial impact on various regulatory requirements.

  20. Using Performance Reference Compounds (PRCs) to measure dissolved water concentrations (Cfree) in the water column: Assessing equilibrium models

    EPA Science Inventory

    Equilibrium-based passive sampling methods are often used in aquatic environmental monitoring to measure hydrophobic organic contaminants (HOCs) and in the subsequent evaluation of their effects on ecological and human health. HOCs freely dissolved in water (Cfree) will partition...

  1. The effect of membrane filtration artifacts on dissolved trace element concentrations

    USGS Publications Warehouse

    Horowitz, A.J.; Elrick, K.A.; Colberg, M.R.

    1992-01-01

    Among environment scientists, the current and almost universally accepted definition of dissolved constituents is an operational one only those materials which pass through a 0.45-??m membrane filter are considered to be dissolved. Detailed laboratory and field studies on Fe and Al indicate that a number of factors associated with filtration, other than just pore size, can substantially alter 'dissolved' trace element concentrations; these include: filter type, filter diameter, filtration method, volume of sample processed, suspended sediment concentration, suspended sediment grain-size distribution, concentration of colloids and colloidally-associated trace elements and concentration of organic matter. As such, reported filtered-water concentrations employing the same pore size filter may not be equal. Filtration artifacts may lead to the production of chemical data that indicate seasonal or annual 'dissolved' chemical trends which do not reflect actual environmental conditions. Further, the development of worldwide averages for various dissolved chemical constituents, the quantification of geochemical cycles, and the determination of short- or long-term environmental chemical trends may be subject to substantial errors, due to filtration artifacts, when data from the same or multiple sources are combined. Finally, filtration effects could have a substantial impact on various regulatory requirements.

  2. Dissolved gas concentrations of the geothermal fluids in Taiwan

    NASA Astrophysics Data System (ADS)

    Chen, Ai-Ti; Yang, Tsanyao Frank

    2010-05-01

    Taiwan, a geologically active island, is located on the boundary of the Philippine Sea Plate and the Eurasian Plate. High heat flow and geothermal gradient generated by the complex collision and orogeny, warm up the meteoric water and/or the ground water. The heated water becomes geothermal fluids. In previous studies, researchers tried to categorize hot springs based on the appearance, chemical compositions and lithological areas. Because of the chemical inertness, the concentrations and isotopic composition of dissolved noble gases are good indicators of the mantle degassing, geothermal conditions, and so on. In this study, 55 hot springs were collected from different tectonic units. It is the first time to systematically study the hot springs in Taiwan in terms of dissolved gases. Hot spring water is sampled and stored in pre-evacuated glass bottles for analyzing gas compositions. The abundances of noble gases were determined by a quadrupole mass spectrometer based on the isotope dilution technique. Samples with glass vials are introduced to RAD 7 and GC for dissolved Rn and major dissolved gases analyses. Furthermore, helium isotopic ratios and helium-neon ratios are measured on a conventional noble gas mass spectrometer. For hydrochemistry analysis, water samples are analyzed by IC, ICP-MS and titration. We can classify the hot springs samples into three major groups from main anion concentration data; and then, subdivide them into nine minor groups by cation concentration data. Moreover, according to major dissolved gases compositions, three major gas components: CH4, N2 and CO2, are identified. Dissolved noble gases provided more detailed clues about hot springs sources in Taiwan, such as the degree of mixing between meteoric water and deep-source water, which will be further discussed in this study.

  3. The effect of membrane filtration on dissolved trace element concentrations

    USGS Publications Warehouse

    Horowitz, A.J.; Lum, K.R.; Garbarino, J.R.; Hall, G.E.M.; Lemieux, C.; Demas, C.R.

    1996-01-01

    The almost universally accepted operational definition for dissolved constituents is based on processing whole-water samples through a 0.45-??m membrane filter. Results from field and laboratory experiments indicate that a number of factors associated with filtration, other than just pore size (e.g., diameter, manufacturer, volume of sample processed, amount of suspended sediment in the sample), can produce substantial variations in the 'dissolved' concentrations of such elements as Fe, Al, Cu, Zn, Pb, Co, and Ni. These variations result from the inclusion/exclusion of colloidally- associated trace elements. Thus, 'dissolved' concentrations quantitated by analyzing filtrates generated by processing whole-water through similar pore- sized membrane filters may not be equal/comparable. As such, simple filtration through a 0.45-??m membrane filter may no longer represent an acceptable operational definition for dissolved chemical constituents. This conclusion may have important implications for environmental studies and regulatory agencies.

  4. Seasonality of diel cycles of dissolved trace-metal concentrations in a Rocky Mountain stream

    USGS Publications Warehouse

    Nimick, D.A.; Cleasby, T.E.; McCleskey, R. Blaine

    2005-01-01

    Substantial diel (24-h) cycles in dissolved (0.1-??m filtration) metal concentrations were observed during summer low flow, winter low flow, and snowmelt runoff in Prickly Pear Creek, Montana. During seven diel sampling episodes lasting 34-61.5 h, dissolved Mn and Zn concentrations increased from afternoon minimum values to maximum values shortly after sunrise. Dissolved As concentrations exhibited the inverse timing. The magnitude of diel concentration increases varied in the range 17-152% for Mn and 70-500% for Zn. Diel increases of As concentrations (17-55%) were less variable. The timing of minimum and maximum values of diel streamflow cycles was inconsistent among sampling episodes and had little relation to the timing of metal concentration cycles, suggesting that geochemical rather than hydrological processes are the primary control of diel metal cycles. Diel cycles of dissolved metal concentrations should be assumed to occur at any time of year in any stream with dissolved metals and neutral to alkaline pH. ?? Springer-Verlag 2005.

  5. Influence of dissolved oxygen concentration on the pharmacokinetics of alcohol in humans.

    PubMed

    Baek, In-hwan; Lee, Byung-yo; Kwon, Kwang-il

    2010-05-01

    Ethanol oxidation by the microsomal ethanol oxidizing system requires oxygen for alcohol metabolism, and a higher oxygen uptake increases the rate of ethanol oxidation. We investigated the effect of dissolved oxygen on the pharmacokinetics of alcohol in healthy humans (n = 49). The concentrations of dissolved oxygen were 8, 20, and 25 ppm in alcoholic drinks of 240 and 360 ml (19.5% v/v). Blood alcohol concentrations (BACs) were determined by converting breath alcohol concentrations. Breath samples were collected every 30 min when the BAC was higher than 0.015%, 20 min at BAC < or =0.015%, 10 min at BAC < or =0.010%, and 5 min at BAC < or =0.006%. The high dissolved oxygen groups (20, 25 ppm) descended to 0.000% and 0.050% BAC faster than the normal dissolved oxygen groups (8 ppm; p < 0.05). In analyzing pharmacokinetic parameters, AUC(inf) and K(el) of the high oxygen groups were lower than in the normal oxygen group, while C(max) and T(max) were not significantly affected. In a Monte Carlo simulation, the lognormal distribution of mean values of AUC(inf) and t(1/2) was expected to be reduced in the high oxygen group compared to the normal oxygen group. In conclusion, elevated dissolved oxygen concentrations in alcoholic drinks accelerate the metabolism and elimination of alcohol. Thus, enhanced dissolved oxygen concentrations in alcohol may have a role to play in reducing alcohol-related side effects and accidents.

  6. Bubble growth as a means to measure dissolved nitrogen concentration in aerated water

    NASA Astrophysics Data System (ADS)

    Ando, Keita; Yamashita, Tatsuya

    2017-11-01

    Controlling the amount of dissolved gases in water is important, for example, to food processing; it is essential to quantitatively evaluate dissolved gas concentration. The concentration of dissolved oxygen (DO) can be measured by commercial DO meters, but that of dissolved nitrogen (DN) cannot be obtained easily. Here, we propose a means to measure DN concentration based on Epstein-Plesset-type analysis of bubble growth under dissolved gas supersaturation. DO supersaturation in water is produced by oxygen microbubble aeration. The diffusion-driven growth of bubbles nucleated at glass surfaces in contact with the aerated water is first observed. The observed growth is then compared to the extended Epstein-Plesset theory that considers Fick's mass transfer of both DO and DN across bubble interfaces; in this comparison, the unknown DN concentration is treated as a fitting parameter. Comparisons between the experiment and the theory suggest, as expected, that DN can be effectively purged by oxygen microbubble aeration. This study was supported in part by the Mizuho Foundation for the Promotion of Science and by a MEXT Grant-in-Aid for the Program for Leading Graduate Schools.

  7. Dissolved Platinum Concentrations in Coastal Seawater: Boso to Sanriku Areas, Japan.

    PubMed

    Mashio, Asami Suzuki; Obata, Hajime; Gamo, Toshitaka

    2017-08-01

    Platinum, one of the rarest elements in the earth's crust, is now widely used in a range of products, such as catalytic converters in automobiles and anticancer drugs. Increasing use and dispersal of platinum has the potential to affect aquatic environments. Platinum concentrations in open ocean seawater have been found to be very low (approximately 0.2 pmol/L); however, Pt distributions and biogeochemical cycles in coastal areas are unknown. In this study, we investigated Pt concentrations in coastal waters between the Boso and Sanriku areas, Japan, after the 2011 tsunami. We determined sub-picomolar levels of dissolved Pt using isotope-dilution Inductively coupled plasma mass spectrometry after column preconcentration with an anion exchange resin. Dissolved Pt concentrations were found to be in the range 0.20-1.5 pmol/L, with the highest concentration in bottom water of the Boso coastal area, and at stations close to Tokyo Bay. Assuming thermodynamical equilibrium, Pt was determined to be present in the form PtCl 5 (OH) 2- , even in low-oxygen coastal waters. Vertical profiles indicated Pt levels increased toward seafloors near coastal stations and were similar to those of the open ocean at trench stations. High concentrations of dissolved Pt are thought to be derived from coastal sediments.

  8. Hydrological and Geochemical Influences on the Dissolved Silica Concentrations in Natural Water in a Steep Headwater Catchment

    NASA Astrophysics Data System (ADS)

    Asano, Y.; Uchida, T.; Ohte, N.

    2002-12-01

    Dissolved silica has been used as a useful indicator of a chemical weathering in many geochemical studies in natural environment. Previous hydrological studies indicated that various hydrological processes affect the dissolution and precipitation of silica in hillslope and transport of this silica to stream; however, information is still limited to link this knowledge to understand geochemical processes. The observations of dissolved silica concentration in groundwater, spring and stream water was conducted at the unchannelled hillslope in the Tanakami Mountains of central Japan; (1) to clarify the effects of preferential flowpaths including lateral and vertical flow in soil layer and flow through bedrock fracture in the variation of dissolved silica concentration in runoff and groundwater, and (2) to isolate the effects of mixing of water from geochemically diverse water sources on the dissolved silica concentration. The mean dissolved silica concentrations in soil water at 40 cm depth and transient groundwater formed in upslope area were relatively constant independent of the variation in the new water ratio. The mean dissolved silica concentrations were similar regardless of the sampling depth in soil although the mean residence times of water increase with depth. These results indicated that dissolved silica concentrations in soil water and transient groundwater were defined almost independent of contact time of water with minerals. While the mean dissolved silica concentration in perennial groundwater, which was recharged by infiltrating water through soil and water emerging from bedrock in a area near to spring, was more than twice that of transient groundwater and the variation was relatively large. The mean dissolved silica concentration increased significantly at downslope from perennial groundwater, spring to the stream and the spring and stream concentrations also showed large variation. The dissolved silica concentrations of those perennial groundwater

  9. Fluoride, Nitrate, and Dissolved-Solids Concentrations in Ground Waters of Washington

    USGS Publications Warehouse

    Lum, W. E.; Turney, Gary L.

    1984-01-01

    This study provides basic data on ground-water quality throughout the State. It is intended for uses in planning and management by agencies and individuals who have responsibility for or interest in, public health and welfare. It also provides a basis for directing future studies of ground-water quality toward areas where ground-water quality problems may already exist. The information presented is a compilation of existing data from numerous sources including: the Washington Departments of Ecology and Social and Health Services, the Environmental Protection Agency, as well as many other local, county, state and federal agencies and private corporations. Only data on fluoride, nitrate, and dissolved-solids concentrations in ground water are presented, as these constituents are among those commonly used to determine the suitability of water for drinking or other purposes. They also reflect both natural and man-imposed effects on water quality and are the most readily available water-quality data for the State of Washington. The percentage of wells with fluoride, nitrate, or dissolved-solids concentrations exceeding U.S. Environmental Protection Agency Primary and Secondary Drinking Water Regulations were about 1, about 3, and about 3, respectively. Most high concentrations occurred in widely separated wells. Two exceptions were: high concentrations of nitrate and dissolved solids in wells on the Hanford Department of Energy Facility and high concentrations of nitrate in the lower Yakima River basin. (USGS)

  10. Tracking Dissolved Methane Concentrations near Active Seeps and Gas Hydrates: Sea of Japan.

    NASA Astrophysics Data System (ADS)

    Snyder, G. T.; Aoki, S.; Matsumoto, R.; Tomaru, H.; Owari, S.; Nakajima, R.; Doolittle, D. F.; Brant, B.

    2015-12-01

    A number of regions in the Sea of Japan are known for active gas venting and for gas hydrate exposures on the sea floor. In this investigation we employed several gas sensors mounted on a ROV in order to determine the concentrations of dissolved methane in the water near these sites. Methane concentrations were determined during two-second intervals throughout each ROV deployment during the cruise. The methane sensor deployments were coupled with seawater sampling using Niskin bottles. Dissolved gas concentrations were later measured using gas chromatography in order to compare with the sensor results taken at the same time. The observed maximum dissolved methane concentrations were much lower than saturation values, even when the ROV manipulators were in contact with gas hydrate. Nonetheless, dissolved concentrations did reach several thousands of nmol/L near gas hydrate exposures and gas bubbles, more than two orders of magnitude over the instrumental detection limits. Most of the sensors tested were able to detect dissolved methane concentrations as low as 10 nmol/L which permitted detection when the ROV approached methane plume sites, even from several tens of meters above the sea floor. Despite the low detection limits, the methane sensors showed variable response times when returning to low-background seawater (~5nM). For some of the sensors, the response time necessary to return to background values occurred in a matter of minutes, while for others it took several hours. Response time, as well as detection limit, should be an important consideration when selecting methane sensors for ROV or AUV investigations. This research was made possible, in part, through funding provided by the Japanese Ministry of Economy, Trade and Industry (METI).

  11. Investigating Factors that Affect Dissolved Oxygen Concentration in Water

    ERIC Educational Resources Information Center

    Jantzen, Paul G.

    1978-01-01

    Describes activities that demonstrate the effects of factors such as wind velocity, water temperature, convection currents, intensity of light, rate of photosynthesis, atmospheric pressure, humidity, numbers of decomposers, presence of oxidizable ions, and respiration by plants and animals on the dissolved oxygen concentration in water. (MA)

  12. Trends in nitrate and dissolved-solids concentrations in ground water, Carson Valley, Douglas County, Nevada, 1985-2001

    USGS Publications Warehouse

    Rosen, Michael R.

    2003-01-01

    Analysis of trends in nitrate and total dissolved-solids concentrations over time in Carson Valley, Nevada, indicates that 56 percent of 27 monitoring wells that have long-term records of nitrate concentrations show increasing trends, 11 percent show decreasing trends, and 33 percent have not changed. Total dissolved-solids concentrations have increased in 52 percent of these wells and are stable in 48 percent. None of these wells show decreasing trends in total dissolved-solids concentrations. The wells showing increasing trends in nitrate and total dissolved-solids concentrations were always in areas that use septic waste-disposal systems. Therefore, the primary cause of these increases is likely the increase in septic-tank usage over the past 40 years.

  13. Concentrations of dissolved oxygen in the lower Puyallup and White rivers, Washington, August and September 2000 and 2001

    USGS Publications Warehouse

    Ebbert, J.C.

    2002-01-01

    The U.S. Geological Survey, Washington State Department of Ecology, and Puyallup Tribe of Indians conducted a study in August and September 2001 to assess factors affecting concentrations of dissolved oxygen in the lower Puyallup and White Rivers, Washington. The study was initiated because observed concentrations of dissolved oxygen in the lower Puyallup River fell to levels ranging from less than 1 milligram per liter (mg/L) to about 6 mg/L on several occasions in September 2000. The water quality standard for the concentration of dissolved oxygen in the Puyallup River is 8 mg/L.This study concluded that inundation of the sensors with sediment was the most likely cause of the low concentrations of dissolved oxygen observed in September 2000. The conclusion was based on (1) knowledge gained when a dissolved-oxygen sensor became covered with sediment in August 2001, (2) the fact that, with few exceptions, concentrations of dissolved oxygen in the lower Puyallup and White Rivers did not fall below 8 mg/L in August and September 2001, and (3) an analysis of other mechanisms affecting concentrations of dissolved oxygen.The analysis of other mechanisms indicated that they are unlikely to cause steep declines in concentrations of dissolved oxygen like those observed in September 2000. Five-day biochemical oxygen demand ranged from 0.22 to 1.78 mg/L (mean of 0.55 mg/L), and river water takes only about 24 hours to flow through the study reach. Photosynthesis and respiration cause concentrations of dissolved oxygen in the lower Puyallup River to fluctuate as much as about 1 mg/L over a 24-hour period in August and September. Release of water from Lake Tapps for the purpose of hydropower generation often lowered concentrations of dissolved oxygen downstream in the White River by about 1 mg/L. The effect was smaller farther downstream in the Puyallup River at river mile 5.8, but was still observable as a slight decrease in concentrations of dissolved oxygen caused by

  14. Impact of dissolved oxygen concentration on some key parameters and production of rhG-CSF in batch fermentation.

    PubMed

    Krishna Rao, Dasari V; Ramu, Chatadi T; Rao, Joginapally V; Narasu, Mangamoori L; Bhujanga Rao, Adibhatla Kali S

    2008-09-01

    The impact of different levels of agitation speed, carbondioxide and dissolved oxygen concentration on the key parameters and production of rhG-CSF in Escherichia coli BL21(DE3)PLysS were studied. Lower carbondioxide concentrations as well as higher agitation speeds and dissolved oxygen concentrations led to reduction in the acetate concentrations, and enhanced the cell growth, but inhibited plasmid stability and rhG-CSF expression. Similarly, higher carbondioxide concentrations and lower agitation speeds as well as dissolved oxygen concentrations led to enhanced acetate concentrations, but inhibited the cell growth and protein expression. To address the bottlenecks, a two-stage agitation control strategy (strategy-1) and two-stage dissolved oxygen control strategy (strategy-2) were employed to establish the physiological and metabolic conditions, so as to improve the expression of rhG-CSF. By adopting strategy-1 the yields were improved 1.4-fold over constant speed of 550 rpm, 1.1-fold over constant dissolved oxygen of 45%, respectively. Similarly, using strategy-2 the yields were improved 1.6-fold over constant speed of 550 rpm, 1.3-fold over constant dissolved oxygen of 45%, respectively.

  15. DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    P. Bernot

    The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of elements with radioactive isotopes under probable repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, field measurements, and laboratory experiments. The scope of this activity is to predict dissolved concentrations or solubility limits for elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) relevant to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are provided in the form of tabulated functions with pH andmore » log fCO{sub 2} as independent variables, plus one or more uncertainty terms. The solubility limits for the remaining elements are either in the form of distributions or single values. Even though selection of an appropriate set of radionuclides documented in Radionuclide Screening (BSC 2002 [DIRS 160059]) includes actinium, transport of Ac is not modeled in the total system performance assessment for the license application (TSPA-LA) model because of its extremely short half-life. Actinium dose is calculated in the TSPA-LA by assuming secular equilibrium with {sup 231}Pa (Section 6.10); therefore, Ac is not analyzed in this report. The output data from this report are fundamental inputs for TSPA-LA used to determine the estimated release of these elements from waste packages and the engineered barrier system. Consistent modeling approaches and environmental conditions were used to develop solubility models for the actinides discussed in this report. These models cover broad ranges of environmental conditions so they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified

  16. Novel Apparatus for the Real-Time Quantification of Dissolved Gas Concentrations and Isotope Ratios

    NASA Astrophysics Data System (ADS)

    Gupta, M.; Leen, J.; Baer, D. S.; Owano, T. G.; Liem, J.

    2013-12-01

    Measurements of dissolved gases and their isotopic composition are critical in studying a variety of phenomena, including underwater greenhouse gas generation, air-surface exchange, and pollution migration. These studies typically involve obtaining water samples from streams, lakes, or ocean water and transporting them to a laboratory, where they are degased. The gases obtained are then generally measured using gas chromatography and isotope ratio mass spectrometry for concentrations and isotope ratios, respectively. This conventional, off-line methodology is time consuming, significantly limits the number of the samples that can be measured and thus severely inhibits detailed spatial and temporal mapping of gas concentrations and isotope ratios. In this work, we describe the development of a new membrane-based degassing device that interfaces directly to Los Gatos Research (cavity enhanced laser absorption or Off-Axis ICOS) gas analyzers (cavity enhanced laser absorption or Off-Axis ICOS analyzers) to create an autonomous system that can continuously and quickly measure concentrations and isotope ratios of dissolved gases in real time in the field. By accurately controlling the water flow rate through the membrane degasser, gas pressure on the outside of the membrane, and water pressure on the inside of the membrane, the system is able to generate precise and highly reproducible results. Moreover, by accurately measuring the gas flow rates in and out of the degasser, the gas-phase concentrations (ppm) could be converted into dissolved gas concentrations (nM). We will present detailed laboratory test data that quantifies the linearity, precision, and dynamic range of the system for the concentrations and isotope ratios of dissolved methane, carbon dioxide, and nitrous oxide. By interfacing the degassing device to a novel cavity-enhanced spectrometer (developed by LGR), preliminary data will also be presented for dissolved volatile organics (VOC) and other

  17. Water quality and processes affecting dissolved oxygen concentrations in the Blackwater River, Canaan Valley, West Virginia

    USGS Publications Warehouse

    Waldron, M.C.; Wiley, J.B.

    1996-01-01

    The water quality and environmental processes affecting dissolved oxygen were determined for the Blackwater River in Canaan Valley, West Virginia. Canaan Valley is oval-shaped (14 miles by 5 miles) and is located in the Allegheny Mountains at an average elevation of 3,200 feet above sea level. Tourism, population, and real estate development have increased in the past two decades. Most streams in Canaan Valley are a dilute calcium magnesium bicarbonate-type water. Streamwater typicaly was soft and low in alkalinity and dissolved solids. Maximum values for specific conductance, hardness, alkalinity, and dissolved solids occurred during low-flow periods when streamflow was at or near baseflow. Dissolved oxygen concentrations are most sensitive to processes affecting the rate of reaeration. The reaeration is affected by solubility (atmospheric pressure, water temperature, humidity, and cloud cover) and processes that determine stream turbulence (stream depth, width, velocity, and roughness). In the headwaters, photosynthetic dissolved oxygen production by benthic algae can result in supersaturated dissolved oxygen concentrations. In beaver pools, dissolved oxygen consumption from sediment oxygen demand and carbonaceous biochemical oxygen demand can result in dissolved oxygen deficits.

  18. Mesocosm validation of the marine No Effect Concentration of dissolved copper derived from a species sensitivity distribution.

    PubMed

    Foekema, E M; Kaag, N H B M; Kramer, K J M; Long, K

    2015-07-15

    The Predicted No Effect Concentration (PNEC) for dissolved copper based on the species sensitivity distribution (SSD) of 24 marine single species tests was validated in marine mesocosms. To achieve this, the impact of actively maintained concentrations of dissolved copper on a marine benthic and planktonic community was studied in 18 outdoor 4.6m(3) mesocosms. Five treatment levels, ranging from 2.9 to 31μg dissolved Cu/L, were created in triplicate and maintained for 82days. Clear effects were observed on gastropod and bivalve molluscs, phytoplankton, zooplankton, sponges and sessile algae. The most sensitive biological endpoints; reproduction success of the bivalve Cerastoderma edule, copepod population development and periphyton growth were significantly affected at concentrations of 9.9μg Cu/L and higher. The No Observed Effect Concentration (NOEC) derived from this study was 5.7μg dissolved Cu/L. Taking into account the DOC concentration of the mesocosm water this NOEC is comparable to the PNEC derived from the SSD. Copyright © 2015. Published by Elsevier B.V.

  19. Rare earth element concentrations in dissolved and acid available particulate forms for eastern UK rivers

    NASA Astrophysics Data System (ADS)

    Neal, C.

    2007-01-01

    Variations in concentration of yttrium (Y), lanthanum (La), cerium (Ce), neodymium (Nd), samarium (Sm) and gadolinium (Gd) among rivers of eastern England and the border with Scotland are described in relation to the dissolved (<0.45 µM) fraction and acid-available particulate (AAP) fractions. The rivers cover a range of rural, agricultural and urban/industrial environments. Yttrium and the lanthanides show significant levels of both dissolved and acid-available particulate forms (typically about 40% in the dissolved form). For the dissolved phase, Y and the lanthanides are linearly correlated with each other and with iron: most of this dissolved component may be in a micro-particulate/colloidal form. The Y and lanthanide relationships show marked scatter and there are anomalously high La concentrations at times for the rivers Great Ouse, Thames and Wear that are probably linked to pollutant sources. For the Ouse, and especially for one of its tributaries, the Swale, relatively high Sm concentrations are probably associated with mineralisation within the catchment and contamination of the associated flood plain. For the AAP components, there are strong linear relationships with Y and the lanthanides across all the rivers. There is also a strong link between these AAP associated REE and AAP iron, although the scatter is greater and the industrial rivers have a lower lanthanide to iron ratio, probably due to iron-rich contaminants.

  20. ACUTE SENSITIVITY OF JUVENILE SHORTNOSE STURGEON TO LOW DISSOLVED OXYGEN CONCENTRATIONS

    EPA Science Inventory

    Campbell, Jed G. and Larry R. Goodman. 2004. Acute Sensitivity of Juvenile Shortnose Sturgeon to Low Dissolved Oxygen Concentrations. EPA/600/J-04/175. Trans. Am. Fish. Soc. 133(3):772-776. (ERL,GB 1155).

    There is considerable concern that factors such as eutrophication, ...

  1. Modeling chlorophyll-a and dissolved oxygen concentration in tropical floodplain lakes (Paraná River, Brazil).

    PubMed

    Rocha, R R A; Thomaz, S M; Carvalho, P; Gomes, L C

    2009-06-01

    The need for prediction is widely recognized in limnology. In this study, data from 25 lakes of the Upper Paraná River floodplain were used to build models to predict chlorophyll-a and dissolved oxygen concentrations. Akaike's information criterion (AIC) was used as a criterion for model selection. Models were validated with independent data obtained in the same lakes in 2001. Predictor variables that significantly explained chlorophyll-a concentration were pH, electrical conductivity, total seston (positive correlation) and nitrate (negative correlation). This model explained 52% of chlorophyll variability. Variables that significantly explained dissolved oxygen concentration were pH, lake area and nitrate (all positive correlations); water temperature and electrical conductivity were negatively correlated with oxygen. This model explained 54% of oxygen variability. Validation with independent data showed that both models had the potential to predict algal biomass and dissolved oxygen concentration in these lakes. These findings suggest that multiple regression models are valuable and practical tools for understanding the dynamics of ecosystems and that predictive limnology may still be considered a powerful approach in aquatic ecology.

  2. Determination of the partition coefficient between dissolved organic carbon and seawater using differential equilibrium kinetics.

    PubMed

    Kim, Du Yung; Kwon, Jung-Hwan

    2018-05-04

    Because the freely dissolved fraction of highly hydrophobic organic chemicals is bioavailable, knowing the partition coefficient between dissolved organic carbon and water (K DOCw ) is crucial to estimate the freely dissolved fraction from the total concentration. A kinetic method was developed to obtain K DOCw that required a shorter experimental time than equilibrium methods. The equilibrium partition coefficients of four polychlorinated biphenyls (PCBs) (2,4,4'-trichlorobiphenyl (PCB 28), 2,2',3,5'-tetrachlorobiphenyl (PCB 44), 2,2',4,5,5'-pentachlorobiphenyl (PCB 101), and 2,2',4,4',5,5'-hexachlorobiphenyl (PCB 153)) between dissolved organic carbon and seawater (K DOCsw ) were determined using seawater samples from the Korean coast. The log K DOCsw values of PCB 28 were measured by equilibrating PCB 28, the least hydrophobic congener, with seawater samples, and the values ranged from 6.60 to 7.20. For the more hydrophobic PCBs (PCB 44, PCB 101, and PCB 153), kinetic experiments were conducted to determine the sorption rate constants (k 2 ) and their log K DOCsw values were obtained by comparing their k 2 with that of PCB 28. The calculated log K DOCsw values were 6.57-7.35 for PCB 44, 6.23-7.44 for PCB 101, and 6.35-7.73 for PCB 153. The validity of the proposed method was further confirmed using three less hydrophobic polycyclic aromatic hydrocarbons. This kinetic method shortened the experimental time to obtain the K DOCsw values of the more hydrophobic PCBs, which did not reach phase equilibrium. Copyright © 2018 Elsevier Ltd. All rights reserved.

  3. Development of a pre-concentration system and auto-analyzer for dissolved methane, ethane, propane, and butane concentration measurements with a GC-FID

    NASA Astrophysics Data System (ADS)

    Chepigin, A.; Leonte, M.; Colombo, F.; Kessler, J. D.

    2014-12-01

    Dissolved methane, ethane, propane, and butane concentrations in natural waters are traditionally measured using a headspace equilibration technique and gas chromatograph with flame ionization detector (GC-FID). While a relatively simple technique, headspace equilibration suffers from slow equilibration times and loss of sensitivity due to concentration dilution with the pure gas headspace. Here we present a newly developed pre-concentration system and auto-analyzer for use with a GC-FID. This system decreases the time required for each analysis by eliminating the headspace equilibration time, increases the sensitivity and precision with a rapid pre-concentration step, and minimized operator time with an autoanalyzer. In this method, samples are collected from Niskin bottles in newly developed 1 L plastic sample bags rather than glass vials. Immediately following sample collection, the sample bags are placed in an incubator and individually connected to a multiport sampling valve. Water is pumped automatically from the desired sample bag through a small (6.5 mL) Liqui-Cel® membrane contactor where the dissolved gas is vacuum extracted and directly flushed into the GC sample loop. The gases of interest are preferentially extracted with the Liqui-Cel and thus a natural pre-concentration effect is obtained. Daily method calibration is achieved in the field with a five-point calibration curve that is created by analyzing gas standard-spiked water stored in 5 L gas-impermeable bags. Our system has been shown to substantially pre-concentrate the dissolved gases of interest and produce a highly linear response of peak areas to dissolved gas concentration. The system retains the high accuracy, precision, and wide range of measurable concentrations of the headspace equilibration method while simultaneously increasing the sensitivity due to the pre-concentration step. The time and labor involved in the headspace equilibration method is eliminated and replaced with the

  4. Epstein-Plesset theory based measurements of concentration of nitrogen gases dissolved in aerated water

    NASA Astrophysics Data System (ADS)

    Sasaki, Masashi; Yamashita, Tatsuya; Ando, Keita

    2016-11-01

    Microbubble aeration is used to dissolved gases into water and is an important technique in agriculture and industry. We can measure concentration of dissolved oxygen (DO) in aerated water by commercial DO meters. However, there do not exist commercially available techniques to measure concentration to dissolved nitrogen (DN). In the present study, we propose the method to measure DN in aerated water with the aid of Epstein-Plesset-type analysis. Gas-supersaturated tap water is produced by applying aeration with micro-sized air bubbles and is then stored in a glass container open to the atmosphere. Diffusion-driven growth of bubbles nucleated at the container surface is recorded with a video camera. The bubble growth rate is compare to the extended Epstein-Plesset theory that models mass transfer of both DO and DN into the surface-attached bubbles base on the diffusion equation. Given the DO measurements, we can obtain the DN level by fitting in the comparison.

  5. Problems associated with using filtration to define dissolved trace element concentrations in natural water samples

    USGS Publications Warehouse

    Horowitz, A.J.; Lum, K.R.; Garbarino, J.R.; Hall, G.E.M.; Lemieux, C.; Demas, C.R.

    1996-01-01

    Field and laboratory experiments indicate that a number of factors associated with filtration other than just pore size (e.g., diameter, manufacturer, volume of sample processed, amount of suspended sediment in the sample) can produce significant variations in the 'dissolved' concentrations of such elements as Fe, Al, Cu, Zn, Pb, Co, and Ni. The bulk of these variations result from the inclusion/exclusion of colloidally associated trace elements in the filtrate, although dilution and sorption/desorption from filters also may be factors. Thus, dissolved trace element concentrations quantitated by analyzing filtrates generated by processing whole water through similar pore-sized filters may not be equal or comparable. As such, simple filtration of unspecified volumes of natural water through unspecified 0.45-??m membrane filters may no longer represent an acceptable operational definition for a number of dissolved chemical constituents.

  6. Mitomycin C dissolved in a reversible thermosetting gel: target tissue concentrations in the rabbit eye.

    PubMed

    Ichien, K; Yamamoto, T; Kitazawa, Y; Oguri, A; Ando, H; Kondo, Y

    1997-01-01

    To determine whether a new, reversible thermosetting gel enhances mitomycin C transfer to target ocular tissues in the rabbit eye. A 0.1 ml solution of mitomycin C containing 0.22 microgram, 2.9 micrograms, or 28 micrograms of the agent dissolved in a reversible thermosetting gel consisting of methylcellulose, citric acid, and polyethylene glycol was injected subconjunctivally in 30 New Zealand albino rabbits. Scleral and conjunctival tissues were excised at 0.5, 1, 2, 4, or 24 hours after the injection and mitomycin C concentrations in these tissues were determined by high performance liquid chromatography. The concentration over time was approximated to a single exponential curve, and initial mitomycin C concentrations, time constants, and half life values were determined. Finally, the areas under the curves (AUCs) between 0.5 and 24 hours were calculated. The mitomycin C concentrations in the target tissues were dose dependent and decreased rapidly over 24 hours. Both the initial mitomycin C concentrations as well as AUCs in these eyes treated with mitomycin C, dissolved in a reversible thermosetting gel, were higher than those in eyes treated similarly in a previous study in which the gel was not used. Applied subconjunctivally in the rabbit eye, mitomycin C dissolved in the reversible thermosetting gel enhanced transfer of the agent to the sclera and the conjunctiva.

  7. Linking CDOM spectral absorption to dissolved organic carbon concentrations and loadings in boreal estuaries

    NASA Astrophysics Data System (ADS)

    Asmala, Eero; Stedmon, Colin A.; Thomas, David N.

    2012-10-01

    The quantity of chromophoric dissolved organic matter (CDOM) and dissolved organic carbon (DOC) in three Finnish estuaries (Karjaanjoki, Kyrönjoki and Kiiminkijoki) was investigated, with respect to predicting DOC concentrations and loadings from spectral CDOM absorption measurements. Altogether 87 samples were collected from three estuarine transects which were studied in three seasons, covering a salinity range between 0 and 6.8, and DOC concentrations from 1572 μmol l-1 in freshwater to 222 μmol l-1 in coastal waters. CDOM absorption coefficient, aCDOM(375) values followed the trend in DOC concentrations across the salinity gradient and ranged from 1.67 to 33.4 m-1. The link between DOC and CDOM was studied using a range of wavelengths and algorithms. Wavelengths between 250 and 270 nm gave the best predictions with single linear regression. Total dissolved iron was found to influence the prediction in wavelengths above 520 nm. Despite significant seasonal and spatial differences in DOC-CDOM models, a universal relationship was tested with an independent data set and found to be robust. DOC and CDOM yields (loading/catchment area) from the catchments ranged from 1.98 to 5.44 g C m-2 yr-1, and 1.67 to 11.5 aCDOM(375) yr-1, respectively.

  8. [Influence of the Concentration of Dissolved Oxygen on Embryonic Development of the Common Toad (Bufo bufo)].

    PubMed

    Dmitrieva, E V

    2015-01-01

    Several series of experiments investigating the influence of dissolved oxygen concentrations on the growth rates and mortality in the embryogenesis of the common toad Bufo bufo were carried out. The experiments showed that, when the eggs develop singly, the lack of oxygen does not lead to an increase in mortality by the time of hatching and results only in a change in the dynamics of mortality: mortality occurs at an earlier stage of development than in the conditions of normal access to oxygen. Taking into account the combined effect of the density of eggs and the dissolved oxygen concentration, we increase the accuracy of analysis of the experimental results and improve the interpretation of the results. In the conditions of different initial density of eggs, the impact of the concentration of dissolved oxygen on mortality and rates of development of the common toad embryos is manifested in different ways. At high density, only a small percentage of embryos survives by the time of hatching, and the embryos are significantly behind in their development compared with the individuals that developed in normal oxygen conditions. The lack of oxygen dissolved in the water slows down the development of embryos of the common toad.

  9. Elevated concentrations of dissolved Ba, Fe and Mn in a mangrove subterranean estuary: Consequence of sea level rise?

    NASA Astrophysics Data System (ADS)

    Sanders, Christian J.; Santos, Isaac R.; Barcellos, Renato; Silva Filho, Emmanoel V.

    2012-07-01

    Groundwater underlying a mangrove habitat was studied to determine the geochemical nature of Ba, Fe and Mn as related to dissolved organic carbon (DOC), SO4 and salinity (Sepetiba Bay, Brazil). Wells were placed across geobotanic facies and sampled monthly for a year. We observed non-conservative behavior and elevated concentrations of dissolved metals relative to local end-members (i.e., fresh river water and seawater). Average Ba concentrations were near 2000 nM in an area with low salinity (˜5.3). Dissolved Fe (up to 654 μM) was two orders of magnitude greater in fresh groundwater than in the seaward sampling stations. Manganese concentrations were greatest (112 μM) in the high salinity (˜65) zone, being directly influenced by salinity. Groundwater Ba, Fe and Mn showed differing site specific concentrations, likely related to ion exchange processes and redox-controlled cycling along distinct mangrove facies. The results of this work show that metal concentrations are altered relative to conservative mixing between terrestrial and marine endmembers, illustrating the importance of mangrove subterranean estuaries as biogeochemical reactors. Roughly-estimated submarine groundwater discharge-derived dissolved Ba, Fe and Mn fluxes were at least one order of magnitude greater than river-derived fluxes into Sepetiba Bay.

  10. Long-term simulations of dissolved oxygen concentrations in Lake Trout lakes

    NASA Astrophysics Data System (ADS)

    Jabbari, A.; Boegman, L.; MacKay, M.; Hadley, K.; Paterson, A.; Jeziorski, A.; Nelligan, C.; Smol, J. P.

    2016-02-01

    Lake Trout are a rare and valuable natural resource that are threatened by multiple environmental stressors. With the added threat of climate warming, there is growing concern among resource managers that increased thermal stratification will reduce the habitat quality of deep-water Lake Trout lakes through enhanced oxygen depletion. To address this issue, a three-part study is underway, which aims to: analyze sediment cores to understand the past, develop empirical formulae to model the present and apply computational models to forecast the future. This presentation reports on the computational modeling efforts. To this end, a simple dissolved oxygen sub-model has been embedded in the one-dimensional bulk mixed-layer thermodynamic Canadian Small Lake Model (CSLM). This model is currently being incorporated into the Canadian Land Surface Scheme (CLASS), the primary land surface component of Environment Canada's global and regional climate modelling systems. The oxygen model was calibrated and validated by hind-casting temperature and dissolved oxygen profiles from two Lake Trout lakes on the Canadian Shield. These data sets include 5 years of high-frequency (10 s to 10 min) data from Eagle Lake and 30 years of bi-weekly data from Harp Lake. Initial results show temperature and dissolved oxygen was predicted with root mean square error <1.5 °C and <3 mgL-1, respectively. Ongoing work is validating the model, over climate-change relevant timescales, against dissolved oxygen reconstructions from the sediment cores and predicting future deep-water temperature and dissolved oxygen concentrations in Canadian Lake Trout lakes under future climate change scenarios. This model will provide a useful tool for managers to ensure sustainable fishery resources for future generations.

  11. Dissolved Pesticide and Organic Carbon Concentrations Detected in Surface Waters, Northern Central Valley, California, 2001-2002

    USGS Publications Warehouse

    Orlando, James L.; Jacobson, Lisa A.; Kuivila, Kathryn

    2004-01-01

    Field and laboratory studies were conducted to determine the effects of pesticide mixtures on Chinook salmon under various environmental conditions in surface waters of the northern Central Valley of California. This project was a collaborative effort between the U.S. Geological Survey (USGS) and the University of California. The project focused on understanding the environmental factors that influence the toxicity of pesticides to juvenile salmon and their prey. During the periods January through March 2001 and January through May 2002, water samples were collected at eight surface water sites in the northern Central Valley of California and analyzed by the USGS for dissolved pesticide and dissolved organic carbon concentrations. Water samples were also collected by the USGS at the same sites for aquatic toxicity testing by the Aquatic Toxicity Laboratory at the University of California Davis; however, presentation of the results of these toxicity tests is beyond the scope of this report. Samples were collected to characterize dissolved pesticide and dissolved organic carbon concentrations, and aquatic toxicity, associated with winter storm runoff concurrent with winter run Chinook salmon out-migration. Sites were selected that represented the primary habitat of juvenile Chinook salmon and included major tributaries within the Sacramento and San Joaquin River Basins and the Sacramento?San Joaquin Delta. Water samples were collected daily for a period of seven days during two winter storm events in each year. Additional samples were collected weekly during January through April or May in both years. Concentrations of 31 currently used pesticides were measured in filtered water samples using solid-phase extraction and gas chromatography-mass spectrometry at the U.S. Geological Survey's organic chemistry laboratory in Sacramento, California. Dissolved organic carbon concentrations were analyzed in filtered water samples using a Shimadzu TOC-5000A total organic carbon

  12. Reactive Transport Modeling Investigation of High Dissolved Sulfide Concentrations in Sedimentary Basin Rocks

    NASA Astrophysics Data System (ADS)

    Xie, M.; Mayer, U. K.; MacQuarrie, K. T. B.

    2017-12-01

    Water with total dissolved sulfide in excess of 1 mmol L-1is widely found in groundwater at intermediate depths in sedimentary basins, including regions of the Michigan basin in southeastern Ontario, Canada. Conversely, at deeper and shallower depths, relatively low total dissolved sulfide concentrations have been reported. The mechanisms responsible for the occurrence of these brackish sulfide-containing waters are not fully understood. Anaerobic microbial sulfate reduction is a common process resulting in the formation of high sulfide concentrations. Sulfate reduction rates depend on many factors including the concentration of sulfate, the abundance of organic substances, redox conditions, temperature, salinity and the species of sulfate reducing bacteria (SRB). A sedimentary basin-specific conceptual model considering the effect of salinity on the rate of sulfate reduction was developed and implemented in the reactive transport model MIN3P-THCm. Generic 2D basin-scale simulations were undertaken to provide a potential explanation for the dissolved sulfide distribution observed in the Michigan basin. The model is 440 km in the horizontal dimension and 4 km in depth, and contains fourteen sedimentary rock units including shales, sandstones, limestones, dolostone and evaporites. The main processes considered are non-isothermal density dependent flow, kinetically-controlled mineral dissolution/precipitation and its feedback on hydraulic properties, cation exchange, redox reactions, biogenic sulfate reduction, and hydromechanical coupling due to glaciation-deglaciation events. Two scenarios were investigated focusing on conditions during an interglacial period and the transient evolution during a glaciation-deglaciation cycle. Inter-glaciation simulations illustrate that the presence of high salinity brines strongly suppress biogenic sulfate reduction. The transient simulations show that glaciation-deglaciation cycles can have an impact on the maximum depth of

  13. Mitomycin C dissolved in a reversible thermosetting gel: target tissue concentrations in the rabbit eye

    PubMed Central

    Ichien, K.; Yamamoto, T.; Kitazawa, Y.; Oguri, A.; Ando, H.; Kondo, Y.

    1997-01-01

    AIMS—To determine whether a new, reversible thermosetting gel enhances mitomycin C transfer to target ocular tissues in the rabbit eye.
METHODS—A 0.1 ml solution of mitomycin C containing 0.22 µg, 2.9 µg, or 28 µg of the agent dissolved in a reversible thermosetting gel consisting of methylcellulose, citric acid, and polyethylene glycol was injected subconjunctivally in 30 New Zealand albino rabbits. Scleral and conjunctival tissues were excised at 0.5, 1, 2, 4, or 24 hours after the injection and mitomycin C concentrations in these tissues were determined by high performance liquid chromatography. The concentration over time was approximated to a single exponential curve, and initial mitomycin C concentrations, time constants, and half life values were determined. Finally, the areas under the curves (AUCs) between 0.5 and 24 hours were calculated.
RESULTS—The mitomycin C concentrations in the target tissues were dose dependent and decreased rapidly over 24 hours. Both the initial mitomycin C concentrations as well as AUCs in these eyes treated with mitomycin C, dissolved in a reversible thermosetting gel, were higher than those in eyes treated similarly in a previous study in which the gel was not used.
CONCLUSION—Applied subconjunctivally in the rabbit eye, mitomycin C dissolved in the reversible thermosetting gel enhanced transfer of the agent to the sclera and the conjunctiva.

 PMID:9135413

  14. Long-term trends in dissolved iron and DOC concentration linked to nitrate depletion in riparian soils

    NASA Astrophysics Data System (ADS)

    Musolff, Andreas; Selle, Benny; Fleckenstein, Jan H.; Oosterwoud, Marieke R.; Tittel, Jörg

    2016-04-01

    The instream concentrations of dissolved organic carbon (DOC) are rising in many catchments of the northern hemisphere. Elevated concentrations of DOC, mainly in the form of colored humic components, increase efforts and costs of drinking water purification. In this study, we evaluated a long-term dataset of 110 catchments draining into German drinking water reservoirs in order to assess sources of DOC and drivers of a potential long-term change. The average DOC concentrations across the wide range of different catchments were found to be well explained by the catchment's topographic wetness index. Higher wetness indices were connected to higher average DOC concentrations, which implies that catchments with shallow topography and pronounced riparian wetlands mobilize more DOC. Overall, 37% of the investigated catchments showed a significant long-term increase in DOC concentrations, while 22% exhibited significant negative trends. Moreover, we found that increasing trends in DOC were positively correlated to trends in dissolved iron concentrations at pH≤6 due to remobilization of DOC previously sorbed to iron minerals. Both, increasing trends in DOC and dissolve iron were found to be connected to decreasing trends and low concentrations of nitrate (below ~6 mg/L). This was especially observed in forested catchments where atmospheric N-depositions were the major source for nitrate availability. In these catchments, we also found long-term increases of phosphate concentrations. Therefore, we argue that dissolved iron, DOC and phosphate were jointly released under iron-reducing conditions when nitrate as a competing electron acceptor was too low in concentrations to prevent the microbial iron reduction. In contrast, we could not explain the observed increasing trends in DOC, iron and phosphate concentrations by the long-term trends of pH, sulfate or precipitation. Altogether this study gives strong evidence that both, source and long-term increases in DOC are

  15. Decadal-scale changes in dissolved-solids concentrations in groundwater used for public supply, Salt Lake Valley, Utah

    USGS Publications Warehouse

    Thiros, Susan A.; Spangler, Larry

    2010-01-01

    Basin-fill aquifers are a major source of good-quality water for public supply in many areas of the southwestern United States and have undergone increasing development as populations have grown over time. During 2005, the basin-fill aquifer in Salt Lake Valley, Utah, provided approximately 75,000 acre-feet, or about 29 percent of the total amount of water used by a population of 967,000. Groundwater in the unconsolidated basin-fill deposits that make up the aquifer occurs under unconfined and confined conditions. Water in the shallow unconfined part of the groundwater system is susceptible to near-surface contamination and generally is not used as a source of drinking water. Groundwater for public supply is withdrawn from the deeper unconfined and confined parts of the system, termed the principal aquifer, because yields generally are greater and water quality is better (including lower dissolved-solids concentrations) than in the shallower parts of the system. Much of the water in the principal aquifer is derived from recharge in the adjacent Wasatch Range (mountain-block recharge). In many areas, the principal aquifer is separated from the overlying shallow aquifer by confining layers of less permeable, fine-grained sediment that inhibit the downward movement of water and any potential contaminants from the surface. Nonetheless, under certain hydrologic conditions, human-related activities can increase dissolved-solids concentrations in the principal aquifer and result in groundwater becoming unsuitable for consumption without treatment or mixing with water having lower dissolved-solids concentrations. Dissolved-solids concentrations in areas of the principal aquifer used for public supply typically are less than 500 milligrams per liter (mg/L), the U.S. Environmental Protection Agency (EPA) secondary (nonenforceable) drinking-water standard. However, substantial increases in dissolved-solids concentrations in the principal aquifer have been documented in some

  16. Online dissolved methane and total dissolved sulfide measurement in sewers.

    PubMed

    Liu, Yiwen; Sharma, Keshab R; Fluggen, Markus; O'Halloran, Kelly; Murthy, Sudhir; Yuan, Zhiguo

    2015-01-01

    Recent studies using short-term manual sampling of sewage followed by off-line laboratory gas chromatography (GC) measurement have shown that a substantial amount of dissolved methane is produced in sewer systems. However, only limited data has been acquired to date due to the low frequency and short span of this method, which cannot capture the dynamic variations of in-sewer dissolved methane concentrations. In this study, a newly developed online measuring device was used to monitor dissolved methane concentrations at the end of a rising main sewer network, over two periods of three weeks each, in summer and early winter, respectively. This device uses an online gas-phase methane sensor to measure methane under equilibrium conditions after being stripped from the sewage. The data are then converted to liquid-phase methane concentrations according to Henry's Law. The detection limit and range are suitable for sewer application and can be adjusted by varying the ratio of liquid-to-gas phase volume settings. The measurement presented good linearity (R² > 0.95) during field application, when compared to off-line measurements. The overall data set showed a wide variation in dissolved methane concentration of 5-15 mg/L in summer and 3.5-12 mg/L in winter, resulting in a significant average daily production of 24.6 and 19.0 kg-CH₄/d, respectively, from the network with a daily average sewage flow of 2840 m³/day. The dissolved methane concentration demonstrated a clear diurnal pattern coinciding with flow and sulfide fluctuation, implying a relationship with the wastewater hydraulic retention time (HRT). The total dissolved sulfide (TDS) concentration in sewers can be determined simultaneously with the same principle.

  17. Vertical distribution and temporal dynamics of dissolved 137Cs concentrations in soil water after the Fukushima Dai-ichi Nuclear Power Plant accident.

    PubMed

    Iwagami, Sho; Onda, Yuichi; Tsujimura, Maki; Hada, Manami; Pun, Ishwar

    2017-11-01

    Radiocesium ( 137 Cs) migration from headwater forested areas to downstream rivers has been investigated in many studies since the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, which was triggered by a catastrophic earthquake and tsunami on 11 March 2011. The accident resulted in the release of a huge amount of radioactivity and its subsequent deposition in the environment. A large part of the radiocesium released has been shown to remain in the forest. The dissolved 137 Cs concentration and its temporal dynamics in river water, stream water, and groundwater have been reported, but reports of dissolved 137 Cs concentration in soil water remain sparse. In this study, soil water was sampled, and the dissolved 137 Cs concentrations were measured at five locations with different land-use types (mature/young cedar forest, broadleaf forest, meadow land, and pasture land) in Yamakiya District, located 35 km northwest of FDNPP from July 2011 to October 2012. Soil water samples were collected by suction lysimeters installed at three different depths at each site. Dissolved 137 Cs concentrations were analyzed using a germanium gamma ray detector. The dissolved 137 Cs concentrations in soil water were high, with a maximum value of 2.5 Bq/L in July 2011, and declined to less than 0.32 Bq/L by 2012. The declining trend of dissolved 137 Cs concentrations in soil water was fitted to a two-component exponential model. The rate of decline in dissolved 137 Cs concentrations in soil water (k 1 ) showed a good correlation with the radiocesium interception potential (RIP) of topsoil (0-5 cm) at the same site. Accounting for the difference of 137 Cs deposition density, we found that normalized dissolved 137 Cs concentrations of soil water in forest (mature/young cedar forest and broadleaf forest) were higher than those in grassland (meadow land and pasture land). Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. A data reconnaissance on the effect of suspended-sediment concentrations on dissolved-solids concentrations in rivers and tributaries in the Upper Colorado River Basin

    USGS Publications Warehouse

    Tillman, Fred D.; Anning, David W.

    2014-01-01

    The Colorado River is one of the most important sources of water in the western United States, supplying water to over 35 million people in the U.S. and 3 million people in Mexico. High dissolved-solids loading to the River and tributaries are derived primarily from geologic material deposited in inland seas in the mid-to-late Cretaceous Period, but this loading may be increased by human activities. High dissolved solids in the River causes substantial damages to users, primarily in reduced agricultural crop yields and corrosion. The Colorado River Basin Salinity Control Program was created to manage dissolved-solids loading to the River and has focused primarily on reducing irrigation-related loading from agricultural areas. This work presents a reconnaissance of existing data from sites in the Upper Colorado River Basin (UCRB) in order to highlight areas where suspended-sediment control measures may be useful in reducing dissolved-solids concentrations. Multiple linear regression was used on data from 164 sites in the UCRB to develop dissolved-solids models that include combinations of explanatory variables of suspended sediment, flow, and time. Results from the partial t-test, overall likelihood ratio, and partial likelihood ratio on the models were used to group the sites into categories of strong, moderate, weak, and no-evidence of a relation between suspended-sediment and dissolved-solids concentrations. Results show 68 sites have strong or moderate evidence of a relation, with drainage areas for many of these sites composed of a large percentage of clastic sedimentary rocks. These results could assist water managers in the region in directing field-scale evaluation of suspended-sediment control measures to reduce UCRB dissolved-solids loading.

  19. New method for the direct determination of dissolved Fe(III) concentration in acid mine waters

    USGS Publications Warehouse

    To, T.B.; Nordstrom, D. Kirk; Cunningham, K.M.; Ball, J.W.; McCleskey, R. Blaine

    1999-01-01

    A new method for direct determination of dissolved Fe(III) in acid mine water has been developed. In most present methods, Fe(III) is determined by computing the difference between total dissolved Fe and dissolved Fe(II). For acid mine waters, frequently Fe(II) >> Fe(III); thus, accuracy and precision are considerably improved by determining Fe(III) concentration directly. The new method utilizes two selective ligands to stabilize Fe(III) and Fe(II), thereby preventing changes in Fe reduction-oxidation distribution. Complexed Fe(II) is cleanly removed using a silica-based, reversed-phase adsorbent, yielding excellent isolation of the Fe(III) complex. Iron(III) concentration is measured colorimetrically or by graphite furnace atomic absorption spectrometry (GFAAS). The method requires inexpensive commercial reagents and simple procedures that can be used in the field. Calcium(II), Ni(II), Pb(II), AI(III), Zn(II), and Cd(II) cause insignificant colorimetric interferences for most acid mine waters. Waters containing >20 mg of Cu/L could cause a colorimetric interference and should be measured by GFAAS. Cobalt(II) and Cr(III) interfere if their molar ratios to Fe(III) exceed 24 and 5, respectively. Iron(II) interferes when its concentration exceeds the capacity of the complexing ligand (14 mg/L). Because of the GFAAS elemental specificity, only Fe(II) is a potential interferent in the GFAAS technique. The method detection limit is 2 ??g/L (40 nM) using GFAAS and 20 ??g/L (0.4 ??M) by colorimetry.A new method for direct determination of dissolved Fe(III) in acid mine water has been developed. In most present methods, Fe(III) is determined by computing the difference between total dissolved Fe and dissolved Fe(II). For acid mine waters, frequently Fe(II)???Fe(III); thus, accuracy and precision are considerably improved by determining Fe(III) concentration directly. The new method utilizes two selective ligands to stabilize Fe(III) and Fe(II), thereby preventing changes

  20. Do your extractable TPH concentrations represent dissolved petroleum? An update on applied research

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Zemo, D.A.

    1997-12-31

    Elevated concentrations of {open_quotes}dissolved-phase{close_quotes} extractable total petroleum hydrocarbons (TPH) in groundwater samples can be a significant impediment to site closure in states that regulate groundwater using TPH criteria. These analytical results are inconsistent with petroleum chemistry because of the relatively low water solubility of petroleum products. This paper presents an update of our research into the source of medium- to high-boiling TPH detections in groundwater samples and application of the results to multiple projects. This work follows from a 1995 publication in which positive interferences to the Method 8015M (GC-FID) TPH measurement by soluble, non-petroleum hydrocarbons resulting from intrinsic bioremediationmore » or non-dissolved petroleum adhered to particulates was described. The 1995 paper was largely theoretical and focused on one case study. Since 1995, we have evaluated the source of TPH detections in groundwater at numerous petroleum sites and have demonstrated the significance of interferences to the Method 8015M measurement to the California regulatory community. Our work has shown conclusively that elevated concentrations of extractable TPH are not representative of dissolved petroleum constituents. We have shown that a sample cleanup prior to analysis using silica gel cleanup (to remove polar non-petroleum hydrocarbons) and/or laboratory filtration (to reduce petroleum-affected particulates) is required to overcome the false positives caused by interferences to the Method 8015M measurement.« less

  1. Use of dissolved H2 concentrations to determine distribution of microbially catalyzed redox reactions in anoxic groundwater

    USGS Publications Warehouse

    Lovley, D.R.; Chapelle, F.H.; Woodward, J.C.

    1994-01-01

    The potential for using concentrations of dissolved H2 to determine the distribution of redox processes in anoxic groundwaters was evaluated. In pristine aquifers in which standard geochemical measurements indicated that Fe-(III) reduction, sulfate reduction, or methanogenesis was the terminal electron accepting process (TEAP), the H2 concentrations were similar to the H2 concentrations that have previously been reported for aquatic sediments with the same TEAPs. In two aquifers contaminated with petroleum products, it was impossible with standard geochemical analyses to determine which TEAPs predominated in specific locations. However, the TEAPs predicted from measurements of dissolved H2 were the same as those determined directly through measurements of microbial processes in incubated aquifer material. These results suggest that H2 concentrations may be a useful tool for analyzing the redox chemistry of nonequilibrium groundwaters.

  2. Measuring Concentrations of Dissolved Methane and Ethane and the 13 C of Methane in Shale and Till.

    PubMed

    Hendry, M Jim; Barbour, S Lee; Schmeling, Erin E; Mundle, Scott O C

    2017-01-01

    Baseline characterization of concentrations and isotopic values of dissolved natural gases is needed to identify contamination caused by the leakage of fugitive gases from oil and gas activities. Methods to collect and analyze baseline concentration-depth profiles of dissolved CH 4 and C 2 H 6 and δ 13 C-CH 4 in shales and Quaternary clayey tills were assessed at two sites in the Williston Basin, Canada. Core and cuttings samples were stored in Isojars ® in a low O 2 headspace prior to analysis. Measurements and multiphase diffusion modeling show that the gas concentrations in core samples yield well-defined and reproducible depth profiles after 31-d equilibration. No measurable oxidative loss or production during core sample storage was observed. Concentrations from cuttings and mud gas logging (including IsoTubes ® ) were much lower than from cores, but correlated well. Simulations suggest the lower concentrations from cuttings can be attributed to drilling time, and therefore their use to define gas concentration profiles may have inherent limitations. Calculations based on mud gas logging show the method can provide estimates of core concentrations if operational parameters for the mud gas capture cylinder are quantified. The δ 13 C-CH 4 measured from mud gas, IsoTubes ® , cuttings, and core samples are consistent, exhibiting slight variations that should not alter the implications of the results in identifying the sources of the gases. This study shows core and mud gas techniques and, to a lesser extent, cuttings, can generate high-resolution depth profiles of dissolved hydrocarbon gas concentrations and their isotopes. © 2016, National Ground Water Association.

  3. A Field Evaluation of Performance Reference Compound Based Estimates of Cfree Using Water Column Deployed Passive Samplers

    EPA Science Inventory

    Low-Density polyethylene (LDPE) sheets are often used as passive samplers for aquatic environmental monitoring to measure the freely dissolved concentrations of hydrophobic organic contaminants (HOCs). HOCs that are freely dissolved in water (Cfree) will partition into the LDPE u...

  4. Application of passive sampling for measuring dissolved concentrations of organic contaminants in the water column at three marine superfund sites.

    PubMed

    Burgess, Robert M; Lohmann, Rainer; Schubauer-Berigan, Joseph P; Reitsma, Pamela; Perron, Monique M; Lefkovitz, Lisa; Cantwell, Mark G

    2015-08-01

    Currently, there is an effort under way to encourage remedial project managers at contaminated sites to use passive sampling to collect freely dissolved concentrations (Cfree ) of hydrophobic organic contaminants to improve site assessments. The objective of the present study was to evaluate the use of passive sampling for measuring water column Cfree for several hydrophobic organic contaminants at 3 US Environmental Protection Agency Superfund sites. Sites investigated included New Bedford Harbor (New Bedford, MA, USA), Palos Verdes Shelf (Los Angeles, CA, USA), and Naval Station Newport (Newport, RI, USA); and the passive samplers evaluated were polyethylene, polydimethylsiloxane-coated solid-phase microextraction fibers, semipermeable membrane devices, and polyoxymethylene. In general, the different passive samplers demonstrated good agreement, with Cfree values varying by a factor of 2 to 3. Further, at New Bedford Harbor, where conventional water sample concentrations were also measured (i.e., grab samples), passive sampler-based Cfree values agreed within a factor of 2. These findings suggest that all of the samplers were experiencing and measuring similar Cfree during their respective deployments. Also, at New Bedford Harbor, a strong log-linear, correlative, and predictive relationship was found between polyethylene passive sampler accumulation and lipid-normalized blue mussel bioaccumulation of polychlorinated biphenyls (r(2)  = 0.92, p < 0.05). The present study demonstrates the utility of passive sampling for generating scientifically accurate water column Cfree values, which is critical for making informed environmental management decisions at contaminated sediment sites. Published 2015 SETAC. This article is a US Government work and is in the public domain in the USA.

  5. Dissolved metals and associated constituents in abandoned coal-mine discharges, Pennsylvania, USA. Part 2: Geochemical controls on constituent concentrations

    USGS Publications Warehouse

    Cravotta, C.A.

    2008-01-01

    Water-quality data for discharges from 140 abandoned mines in the Anthracite and Bituminous Coalfields of Pennsylvania reveal complex relations among the pH and dissolved solute concentrations that can be explained with geochemical equilibrium models. Observed values of pH ranged from 2.7 to 7.3 in the coal-mine discharges (CMD). Generally, flow rates were smaller and solute concentrations were greater for low-pH CMD samples; pH typically increased with flow rate. Although the frequency distribution of pH was similar for the anthracite and bituminous discharges, the bituminous discharges had smaller median flow rates; greater concentrations of SO4, Fe, Al, As, Cd, Cu, Ni and Sr; comparable concentrations of Mn, Cd, Zn and Se; and smaller concentrations of Ba and Pb than anthracite discharges with the same pH values. The observed relations between the pH and constituent concentrations can be attributed to (1) dilution of acidic water by near-neutral or alkaline ground water; (2) solubility control of Al, Fe, Mn, Ba and Sr by hydroxide, sulfate, and/or carbonate minerals; and (3) aqueous SO4-complexation and surface-complexation (adsorption) reactions. The formation of AlSO4+ and AlHSO42 + complexes adds to the total dissolved Al concentration at equilibrium with Al(OH)3 and/or Al hydroxysulfate phases and can account for 10-20 times greater concentrations of dissolved Al in SO4-laden bituminous discharges compared to anthracite discharges at pH of 5. Sulfate complexation can also account for 10-30 times greater concentrations of dissolved FeIII concentrations at equilibrium with Fe(OH)3 and/or schwertmannite (Fe8O8(OH)4.5(SO4)1.75) at pH of 3-5. In contrast, lower Ba concentrations in bituminous discharges indicate that elevated SO4 concentrations in these CMD sources could limit Ba concentrations by the precipitation of barite (BaSO4). Coprecipitation of Sr with barite could limit concentrations of this element. However, concentrations of dissolved Pb, Cu, Cd, Zn

  6. Diel cycles in dissolved metal concentrations in streams: Occurrence and possible causes

    USGS Publications Warehouse

    Nimick, David A.; Gammons, Christopher H.; Cleasby, Thomas E.; Madison, James P.; Skaar, Don; Brick, Christine M.

    2003-01-01

    Substantial diel (24‐hour) cycles in dissolved (0.1‐μm filtration) metal concentrations were observed during low flow for 18 sampling episodes at 14 sites on 12 neutral and alkaline streams draining historical mining areas in Montana and Idaho. At some sites, concentrations of Cd, Mn, Ni, and Zn increased as much as 119, 306, 167, and 500%, respectively, from afternoon minimum values to maximum values shortly after sunrise. Arsenic concentrations exhibited the inverse temporal pattern with increases of up to 54%. Variations in Cu concentrations were small and inconsistent. Diel metal cycles are widespread and persistent, occur over a wide range of metal concentrations, and likely are caused primarily by instream geochemical processes. Adsorption is the only process that can explain the inverse temporal patterns of As and the divalent metals. Diel metal cycles have important implications for many types of water‐quality studies and for understanding trace‐metal mobility.

  7. Effect of pulsed corona discharge voltage and feed gas flow rate on dissolved ozone concentration

    DOE Office of Scientific and Technical Information (OSTI.GOV)

    Prasetyaningrum, A., E-mail: ajiprasetyaningrum@gmail.com; Ratnawati,; Jos, B.

    Ozonization is one of the methods extensively used for water purification and degradation of organic materials. Ozone (O{sub 3}) is recognized as a powerful oxidizing agent. Due to its strong oxidability and better environmental friendless, ozone increasing being used in domestic and industrial applications. Current technology in ozone production utilizes several techniques (corona discharge, ultra violet radiation and electrolysis). This experiment aimed to evaluating effect of voltage and gas flow rate on ozone production with corona discharge. The system consists of two net-type stainless steel electrode placed in a dielectric barrier. Three pulsed voltage (20, 30, 40 KV) and flowmore » rate (5, 10, 15 L/min) were prepare for operation variable at high frequency (3.7 kHz) with AC pulsed power supply. The dissolved ozone concentration depends on the applied high-voltage level, gas flow rate and the discharge exposure duration. The ozone concentration increases with decreasing gas flow rate. Dissolved ozone concentrations greater than 200 ppm can be obtained with a minimum voltage 40 kV.« less

  8. Effect of pulsed corona discharge voltage and feed gas flow rate on dissolved ozone concentration

    NASA Astrophysics Data System (ADS)

    Prasetyaningrum, A.; Ratnawati, Jos, B.

    2015-12-01

    Ozonization is one of the methods extensively used for water purification and degradation of organic materials. Ozone (O3) is recognized as a powerful oxidizing agent. Due to its strong oxidability and better environmental friendless, ozone increasing being used in domestic and industrial applications. Current technology in ozone production utilizes several techniques (corona discharge, ultra violet radiation and electrolysis). This experiment aimed to evaluating effect of voltage and gas flow rate on ozone production with corona discharge. The system consists of two net-type stainless steel electrode placed in a dielectric barrier. Three pulsed voltage (20, 30, 40 KV) and flow rate (5, 10, 15 L/min) were prepare for operation variable at high frequency (3.7 kHz) with AC pulsed power supply. The dissolved ozone concentration depends on the applied high-voltage level, gas flow rate and the discharge exposure duration. The ozone concentration increases with decreasing gas flow rate. Dissolved ozone concentrations greater than 200 ppm can be obtained with a minimum voltage 40 kV.

  9. Dissolved heavy metal concentrations of the Kralkızı, Dicle and Batman dam reservoirs in the Tigris River basin, Turkey.

    PubMed

    Varol, Memet

    2013-10-01

    Water samples were collected at monthly intervals during 1 year of monitoring from Kralkızı, Dicle and Batman dam reservoirs in the Tigris River basin to assess the concentrations of dissolved heavy metals and to determine their spatial and seasonal variations. The results indicated that dissolved heavy metal concentrations in the reservoirs were very low, reflecting the natural background levels. The lowest total metal concentrations in the three dam reservoirs were detected at sampling sites close to the dam wall. However, the highest total concentrations were observed at sites, which are located at the entrance of the streams to the reservoirs. Fe, Cr and Ni were the most abundant elements in the reservoirs, whereas Cd and As were the less abundant. The mean concentrations of dissolved metals in the dam reservoirs never exceeded the maximum permitted concentrations established by EC (European Community), WHO and USEPA drinking water quality guidelines. All heavy metals showed significant seasonal variations. As, Cd, Cr, Cu, Fe, Ni and Pb displayed higher values in the dry season, while higher values for Zn in the wet season. Cluster analysis grouped all ten sampling sites into three clusters. Clusters 1 and 2, and cluster 3 corresponded to relatively low polluted and moderate polluted regions, respectively. PCA/FA demonstrated the dissolved metals in the dam reservoirs controlled by natural sources. Copyright © 2013 Elsevier Ltd. All rights reserved.

  10. Hyperosmotic Agents and Antibiotics Affect Dissolved Oxygen and pH Concentration Gradients in Staphylococcus aureus Biofilms

    PubMed Central

    Kiamco, Mia Mae; Atci, Erhan

    2017-01-01

    ABSTRACT Biofilms on wound surfaces are treated topically with hyperosmotic agents, such as medical-grade honey and cadexomer iodine; in some cases, these treatments are combined with antibiotics. Tissue repair requires oxygen, and a low pH is conducive to oxygen release from red blood cells and epithelialization. We investigated the variation of dissolved oxygen concentration and pH with biofilm depth and the variation in oxygen consumption rates when biofilms are challenged with medical-grade honey or cadexomer iodine combined with vancomycin or ciprofloxacin. Dissolved oxygen and pH depth profiles in Staphylococcus aureus biofilms were measured using microelectrodes. The presence of cadexomer iodine with vancomycin or ciprofloxacin on the surface of the biofilm permitted a measurable concentration of oxygen at greater biofilm depths (101.6 ± 27.3 μm, P = 0.02; and 155.5 ± 27.9 μm, P = 0.016, respectively) than in untreated controls (30.1 μm). Decreases in pH of ∼0.6 and ∼0.4 units were observed in biofilms challenged with medical-grade honey alone and combined with ciprofloxacin, respectively (P < 0.001 and 0.01, respectively); the number of bacteria recovered from biofilms was significantly reduced (1.26 log) by treatment with cadexomer iodine and ciprofloxacin (P = 0.002) compared to the untreated control. Combining cadexomer iodine and ciprofloxacin improved dissolved oxygen concentration and penetration depth into the biofilm, while medical-grade honey was associated with a lower pH; not all treatments established a bactericidal effect in the time frame used in the experiments. IMPORTANCE Reports about using hyperosmotic agents and antibiotics against wound biofilms focus mostly on killing bacteria, but the results of these treatments should additionally be considered in the context of how they affect physiologically important parameters, such as oxygen concentration and pH. We confirmed that the combination of a hyperosmotic agent and an antibiotic

  11. Hyperosmotic Agents and Antibiotics Affect Dissolved Oxygen and pH Concentration Gradients in Staphylococcus aureus Biofilms.

    PubMed

    Kiamco, Mia Mae; Atci, Erhan; Mohamed, Abdelrhman; Call, Douglas R; Beyenal, Haluk

    2017-03-15

    Biofilms on wound surfaces are treated topically with hyperosmotic agents, such as medical-grade honey and cadexomer iodine; in some cases, these treatments are combined with antibiotics. Tissue repair requires oxygen, and a low pH is conducive to oxygen release from red blood cells and epithelialization. We investigated the variation of dissolved oxygen concentration and pH with biofilm depth and the variation in oxygen consumption rates when biofilms are challenged with medical-grade honey or cadexomer iodine combined with vancomycin or ciprofloxacin. Dissolved oxygen and pH depth profiles in Staphylococcus aureus biofilms were measured using microelectrodes. The presence of cadexomer iodine with vancomycin or ciprofloxacin on the surface of the biofilm permitted a measurable concentration of oxygen at greater biofilm depths (101.6 ± 27.3 μm, P = 0.02; and 155.5 ± 27.9 μm, P = 0.016, respectively) than in untreated controls (30.1 μm). Decreases in pH of ∼0.6 and ∼0.4 units were observed in biofilms challenged with medical-grade honey alone and combined with ciprofloxacin, respectively ( P < 0.001 and 0.01, respectively); the number of bacteria recovered from biofilms was significantly reduced (1.26 log) by treatment with cadexomer iodine and ciprofloxacin ( P = 0.002) compared to the untreated control. Combining cadexomer iodine and ciprofloxacin improved dissolved oxygen concentration and penetration depth into the biofilm, while medical-grade honey was associated with a lower pH; not all treatments established a bactericidal effect in the time frame used in the experiments. IMPORTANCE Reports about using hyperosmotic agents and antibiotics against wound biofilms focus mostly on killing bacteria, but the results of these treatments should additionally be considered in the context of how they affect physiologically important parameters, such as oxygen concentration and pH. We confirmed that the combination of a hyperosmotic agent and an antibiotic

  12. Effect of catchment land use and soil type on the concentration, quality, and bacterial degradation of riverine dissolved organic matter.

    PubMed

    Autio, Iida; Soinne, Helena; Helin, Janne; Asmala, Eero; Hoikkala, Laura

    2016-04-01

    We studied the effects of catchment characteristics (soil type and land use) on the concentration and quality of dissolved organic matter (DOM) in river water and on the bacterial degradation of terrestrial DOM. The share of organic soil was the strongest predictor of high concentrations of dissolved organic carbon, nitrogen, and phosphorus (DOC, DON, and DOP, respectively), and was linked to DOM quality. Soil type was more important than land use in determining the concentration and quality of riverine DOM. On average, 5-9 % of the DOC and 45 % of the DON were degraded by the bacterial communities within 2-3 months. Simultaneously, the proportion of humic-like compounds in the DOM pool increased. Bioavailable DON accounted for approximately one-third of the total bioavailable dissolved nitrogen, and thus, terrestrial DON can markedly contribute to the coastal plankton dynamics and support the heterotrophic food web.

  13. Glucose concentration alters dissolved oxygen levels in liquid cultures of Beauveria bassiana and affects formation and bioefficacy of blastospores.

    PubMed

    Mascarin, Gabriel Moura; Jackson, Mark A; Kobori, Nilce Naomi; Behle, Robert W; Dunlap, Christopher A; Delalibera Júnior, Ítalo

    2015-08-01

    The filamentous fungus Beauveria bassiana is an economically important pathogen of numerous arthropod pests and is able to grow in submerged culture as filaments (mycelia) or as budding yeast-like blastospores. In this study, we evaluated the effect of dissolved oxygen and high glucose concentrations on blastospore production by submerged cultures of two isolates of B. bassiana, ESALQ1432 and GHA. Results showed that maintaining adequate dissolved oxygen levels coupled with high glucose concentrations enhanced blastospore yields by both isolates. High glucose concentrations increased the osmotic pressure of the media and coincided with higher dissolved oxygen levels and increased production of significantly smaller blastospores compared with blastospores produced in media with lower concentrations of glucose. The desiccation tolerance of blastospores dried to less than 2.6 % moisture was not affected by the glucose concentration of the medium but was isolate dependent. Blastospores of isolate ESALQ1432 produced in media containing 140 g glucose L(-1) showed greater virulence toward whitefly nymphs (Bemisia tabaci) as compared with blastospores produced in media containing 40 g glucose L(-1). These results suggest a synergistic effect between glucose concentration and oxygen availability on changing morphology and enhancing the yield and efficacy of blastospores of B. bassiana, thereby facilitating the development of a cost-effective production method for this blastospore-based bioinsecticide.

  14. The soil organic carbon content of anthropogenically altered organic soils effects the dissolved organic matter quality, but not the dissolved organic carbon concentrations

    NASA Astrophysics Data System (ADS)

    Frank, Stefan; Tiemeyer, Bärbel; Bechtold, Michel; Lücke, Andreas; Bol, Roland

    2016-04-01

    Dissolved organic carbon (DOC) is an important link between terrestrial and aquatic ecosystems. This is especially true for peatlands which usually show high concentrations of DOC due to the high stocks of soil organic carbon (SOC). Most previous studies found that DOC concentrations in the soil solution depend on the SOC content. Thus, one would expect low DOC concentrations in peatlands which have anthropogenically been altered by mixing with sand. Here, we want to show the effect of SOC and groundwater level on the quantity and quality of the dissolved organic matter (DOM). Three sampling sites were installed in a strongly disturbed bog. Two sites differ in SOC (Site A: 48%, Site B: 9%) but show the same mean annual groundwater level of 15 and 18 cm below ground, respectively. The SOC content of site C (11%) is similar to Site B, but the groundwater level is much lower (-31 cm) than at the other two sites. All sites have a similar depth of the organic horizon (30 cm) and the same land-use (low-intensity sheep grazing). Over two years, the soil solution was sampled bi-weekly in three depths (15, 30 and 60 cm) and three replicates. All samples were analyzed for DOC and selected samples for dissolved organic nitrogen (DON) and delta-13C and delta-15N. Despite differences in SOC and groundwater level, DOC concentrations did not differ significantly (A: 192 ± 62 mg/L, B: 163 ± 55 mg/L and C: 191 ± 97 mg/L). At all sites, DOC concentrations exceed typical values for peatlands by far and emphasize the relevance even of strongly disturbed organic soils for DOC losses. Individual DOC concentrations were controlled by the temperature and the groundwater level over the preceding weeks. Differences in DOM quality were clearer. At site B with a low SOC content, the DOC:DON ratio of the soil solution equals the soil's C:N ratio, but the DOC:DON ratio is much higher than the C:N ratio at site A. In all cases, the DOC:DON ratio strongly correlates with delta-13C. There is no

  15. Assessing the concentration, speciation, and toxicity of dissolved metals during mixing of acid-mine drainage and ambient river water downstream of the Elizabeth Copper Mine, Vermont, USA

    USGS Publications Warehouse

    Balistrieri, L.S.; Seal, R.R.; Piatak, N.M.; Paul, B.

    2007-01-01

    The authors determine the composition of a river that is impacted by acid-mine drainage, evaluate dominant physical and geochemical processes controlling the composition, and assess dissolved metal speciation and toxicity using a combination of laboratory, field and modeling studies. Values of pH increase from 3.3 to 7.6 and the sum of dissolved base metal (Cd + Co + Cu + Ni + Pb + Zn) concentrations decreases from 6270 to 100 ??g/L in the dynamic mixing and reaction zone that is downstream of the river's confluence with acid-mine drainage. Mixing diagrams and PHREEQC calculations indicate that mixing and dilution affect the concentrations of all dissolved elements in the reach, and are the dominant processes controlling dissolved Ca, K, Li, Mn and SO4 concentrations. Additionally, dissolved Al and Fe concentrations decrease due to mineral precipitation (gibbsite, schwertmannite and ferrihydrite), whereas dissolved concentrations of Cd, Co, Cu, Ni, Pb and Zn decrease due to adsorption onto newly formed Fe precipitates. The uptake of dissolved metals by aquatic organisms is dependent on the aqueous speciation of the metals and kinetics of complexation reactions between metals, ligands and solid surfaces. Dissolved speciation of Cd, Cu, Ni and Zn in the mixing and reaction zone is assessed using the diffusive gradients in thin films (DGT) technique and results of speciation calculations using the Biotic Ligand Model (BLM). Data from open and restricted pore DGT units indicate that almost all dissolved metal species are inorganic and that aqueous labile or DGT available metal concentrations are generally equal to total dissolved concentrations in the mixing zone. Exceptions occur when labile metal concentrations are underestimated due to competition between H+ and metal ions for Chelex-100 binding sites in the DGT units at low pH values. Calculations using the BLM indicate that dissolved Cd and Zn species in the mixing and reaction zone are predominantly inorganic

  16. Aerobic sludge digestion under low dissolved oxygen concentrations.

    PubMed

    Arunachalam, RaviSankar; Shah, Hemant K; Ju, Lu-Kwang

    2004-01-01

    Low dissolved oxygen (DO) concentrations occur commonly in aerobic digesters treating thickened sludge, with benefits of smaller digester size, much reduced aeration cost, and higher digestion temperature (especially important for plants in colder areas). The effects of low DO concentrations on digestion kinetics were studied using the sludge from municipal wastewater treatment plants in Akron, Ohio, and Los Lunas, New Mexico. The experiments were conducted in both batch digestion and a mixed mode of continuous, fed-batch, and batch operations. The low DO condition was clearly advantageous in eliminating the need for pH control because of the simultaneous occurrence of nitrification and denitrification. However, when compared with fully aerobic (high DO) systems under constant pH control (rare in full-scale plants), low DO concentrations and a higher solids loading had a negative effect on the specific volatile solids (VS) digestion kinetics. Nonetheless, the overall (volumetric) digestion performance depends not only on the specific digestion kinetics, but also the solids concentration, pH, and digester temperature. All of the latter factors favor the low DO digestion of thickened sludge. The significant effect of temperature on low DO digestion was confirmed in the mixed-mode study with the Akron sludge. When compared with the well-known empirical correlation between VS reduction and the product (temperature x solids retention time), the experimental data followed the same trend, but were lower than the correlation predictions. The latter was attributed to the lower digestible VS in the Akron sludge, the slower digestion at low DO concentrations, or both. Through model simulation, the first-order decay constant (kd) was estimated as 0.004 h(-1) in the mixed-mode operations, much lower than those (0.011 to 0.029 h(-1)) obtained in batch digestion. The findings suggested that the interactions among sludges with different treatment ages may have a substantially

  17. Assessing time-integrated dissolved concentrations and predicting toxicity of metals during diel cycling in streams

    USGS Publications Warehouse

    Balistrieri, Laurie S.; Nimick, David A.; Mebane, Christopher A.

    2012-01-01

    Evaluating water quality and the health of aquatic organisms is challenging in systems with systematic diel (24 hour) or less predictable runoff-induced changes in water composition. To advance our understanding of how to evaluate environmental health in these dynamic systems, field studies of diel cycling were conducted in two streams (Silver Bow Creek and High Ore Creek) affected by historical mining activities in southwestern Montana. A combination of sampling and modeling tools were used to assess the toxicity of metals in these systems. Diffusive Gradients in Thin Films (DGT) samplers were deployed at multiple time intervals during diel sampling to confirm that DGT integrates time-varying concentrations of dissolved metals. Thermodynamic speciation calculations using site specific water compositions, including time-integrated dissolved metal concentrations determined from DGT, and a competitive, multiple-metal biotic ligand model incorporated into the Windemere Humic Aqueous Model Version 6.0 (WHAM VI) were used to determine the chemical speciation of dissolved metals and biotic ligands. The model results were combined with previously collected toxicity data on cutthroat trout to derive a relationship that predicts the relative survivability of these fish at a given site. This integrative approach may prove useful for assessing water quality and toxicity of metals to aquatic organisms in dynamic systems and evaluating whether potential changes in environmental health of aquatic systems are due to anthropogenic activities or natural variability.

  18. Dissolved organic carbon concentrations and compositions, and trihalomethane formation potentials in waters from agricultural peat soils, Sacramento-San Joaquin Delta, California; implications for drinking-water quality

    USGS Publications Warehouse

    Fujii, Roger; Ranalli, Anthony J.; Aiken, George R.; Bergamaschi, Brian A.

    1998-01-01

    Water exported from the Sacramento-San Joaquin River delta (Delta) is an important drinking-water source for more than 20 million people in California. At times, this water contains elevated concentrations of dissolved organic carbon and bromide, and exceeds the U.S. Environmental Protection Agency's maximum contaminant level for trihalomethanes of 0.100 milligrams per liter if chlorinated for drinking water. About 20 to 50 percent of the trihalomethane precursors to Delta waters originates from drainage water from peat soils on Delta islands. This report elucidates some of the factors and processes controlling and affecting the concentration and quality of dissolved organic carbon released from peat soils and relates the propensity of dissolved organic carbon to form trihalomethanes to its chemical composition.Soil water was sampled from near-surface, oxidized, well-decomposed peat soil (upper soil zone) and deeper, reduced, fibrous peat soil (lower soil zone) from one agricultural field in the west central Delta over 1 year. Concentrations of dissolved organic carbon in the upper soil zone were highly variable, with median concentrations ranging from 46.4 to 83.2 milligrams per liter. Concentrations of dissolved organic carbon in samples from the lower soil zone were much less variable and generally slightly higher than samples from the upper soil zone, with median concentrations ranging from 49.3 to 82.3 milligrams per liter. The dissolved organic carbon from the lower soil zone had significantly higher aromaticity (as measured by specific ultraviolet absorbance) and contained significantly greater amounts of aromatic humic substances (as measured by XAD resin fractionation and carbon-13 nuclear magnetic resonance analysis of XAD isolates) than the dissolved organic carbon from the upper soil zone. These results support the conclusion that more aromatic forms of dissolved organic carbon are produced under anaerobic conditions compared to aerobic conditions

  19. Temporal changes in dissolved 137Cs concentrations in groundwater and stream water in Fukushima after the Fukushima Dai-ichi Nuclear Power Plant accident.

    PubMed

    Iwagami, Sho; Tsujimura, Maki; Onda, Yuichi; Nishino, Masataka; Konuma, Ryohei; Abe, Yutaka; Hada, Manami; Pun, Ishwar; Sakaguchi, Aya; Kondo, Hiroaki; Yamamoto, Masayoshi; Miyata, Yoshiki; Igarashi, Yasuhito

    2017-01-01

    The concentration of dissolved 137 Cs in groundwater and stream water in the headwater catchments in Yamakiya district, located ∼35 km north west of Fukushima Dai-ichi Nuclear Power Plant (FDNPP), was monitored from June 2011 to July 2013, after the earthquake and tsunami disaster. Groundwater and stream water were sampled at intervals of approximately 2 months at each site. Intensive sampling was also conducted during rainstorm events. Compared with previous data from the Chernobyl NPP accident, the concentration of dissolved 137 Cs in stream water was low. In the Iboishi-yama catchment, a trend was observed for the concentration of dissolved 137 Cs in stream water to decline, which could be divided into two phases by October 2011 (a fast flush of activity as a result of rapid washoff and a slow decline as a result of soil fixation and redistribution processes). The highest 137 Cs concentration recorded at Iboishi-yama was 1.2 Bq/L on August 6, 2011, which then declined to 0.021-0.049 Bq/L during 2013 (in stream water under normal water-flow conditions). During the rainfall events, the concentration of dissolved 137 Cs in stream water increased temporarily. The concentration of dissolved 137 Cs in groundwater at a depth of 30 m at Iboishi-yama displayed a decreasing trend from 2011 to 2013, with a range from 0.039 Bq/L to 0.0025 Bq/L. The effective half-lives of stream water in the initial fast flush and secondary phases were 0.10-0.21 and 0.69-1.5 y, respectively in the three catchments. The effective half-life of groundwater was 0.46-0.58 y at Koutaishi-yama and 0.50-3.3 y at Iboishi-yama. The trend for the concentration of dissolved 137 Cs to decline in groundwater and stream water was similar throughout 2012-2013, and the concentrations recorded in deeper groundwater were closer to those in stream water. The declining trend of dissolved 137 Cs concentrations in stream water was similar to that of the loss of canopy 137 Cs by throughfall, as shown in

  20. Frequency-duration analysis of dissolved-oxygen concentrations in two southwestern Wisconsin streams

    USGS Publications Warehouse

    Greb, Steven R.; Graczyk, David J.

    2007-01-01

    Historically, dissolved-oxygen (DO) data have been collected in the same manner as other water-quality constituents, typically at infrequent intervals as a grab sample or an instantaneous meter reading. Recent years have seen an increase in continuous water-quality monitoring with electronic dataloggers. This new technique requires new approaches in the statistical analysis of the continuous record. This paper presents an application of frequency-duration analysis to the continuous DO records of a cold and a warm water stream in rural southwestern Wisconsin. This method offers a quick, concise way to summarize large time-series data bases in an easily interpretable manner. Even though the two streams had similar mean DO concentrations, frequency-duration analyses showed distinct differences in their DO-concentration regime. This type of analysis also may be useful in relating DO concentrations to biological effects and in predicting low DO occurrences.

  1. Linking microbial community structure to membrane biofouling associated with varying dissolved oxygen concentrations.

    PubMed

    Gao, Da-wen; Fu, Yuan; Tao, Yu; Li, Xin-xin; Xing, Min; Gao, Xiu-hong; Ren, Nan-qi

    2011-05-01

    In order to elucidate how dissolved oxygen (DO) concentration influenced the generation of extracellular polymeric substance (EPS) and soluble microbial products (SMP) in mixed liquor and biocake, 16S rDNA fingerprinting analyses were performed to investigate the variation of the microbial community in an aerobic membrane bioreactor (MBR). The function of microbial community structure was proved to be ultimately responsible for biofouling. Obvious microbial community succession from the subphylum of Betaproteobacteria to Deltaproteobacteria was observed in biocake. High concentration of EPS in biocake under the low DO concentration (0.5 mg L(-1)) caused severe biofouling. The correlation coefficient of membrane fouling rate with EPS content in biocake (0.9941-0.9964) was much higher than that in mixed liquor (0.6689-0.8004). Copyright © 2011 Elsevier Ltd. All rights reserved.

  2. Temporal evolution of cadmium, copper and lead concentration in the Venice Lagoon water in relation with the speciation and dissolved/particulate partition.

    PubMed

    Morabito, Elisa; Radaelli, Marta; Corami, Fabiana; Turetta, Clara; Toscano, Giuseppa; Capodaglio, Gabriele

    2018-04-01

    In order to study the role of sediment re-suspension and deposition versus the role of organic complexation, we investigated the speciation of cadmium (Cd), copper (Cu) and lead (Pb) in samples collected in the Venice Lagoon during several campaigns from 1992 to 2006. The increment in Cd and Pb concentration in the dissolved phases, observed in the central and northern basins, can be linked to important alterations inside the lagoon caused by industrial and urban factors. The study focuses on metal partition between dissolved and particulate phases. The analyses carried out in different sites illustrate the complex role of organic matter in the sedimentation process. While Cd concentration in sediments can be correlated with organic matter, no such correlation can be established in the case of Pb, whose particulate concentration is related only to the dissolved concentration. In the case of Cu, the role of organic complexation remains unclear. Copyright © 2017 Elsevier Ltd. All rights reserved.

  3. Estimating dissolved organic carbon concentration in turbid coastal waters using optical remote sensing observations

    NASA Astrophysics Data System (ADS)

    Cherukuru, Nagur; Ford, Phillip W.; Matear, Richard J.; Oubelkheir, Kadija; Clementson, Lesley A.; Suber, Ken; Steven, Andrew D. L.

    2016-10-01

    Dissolved Organic Carbon (DOC) is an important component in the global carbon cycle. It also plays an important role in influencing the coastal ocean biogeochemical (BGC) cycles and light environment. Studies focussing on DOC dynamics in coastal waters are data constrained due to the high costs associated with in situ water sampling campaigns. Satellite optical remote sensing has the potential to provide continuous, cost-effective DOC estimates. In this study we used a bio-optics dataset collected in turbid coastal waters of Moreton Bay (MB), Australia, during 2011 to develop a remote sensing algorithm to estimate DOC. This dataset includes data from flood and non-flood conditions. In MB, DOC concentration varied over a wide range (20-520 μM C) and had a good correlation (R2 = 0.78) with absorption due to coloured dissolved organic matter (CDOM) and remote sensing reflectance. Using this data set we developed an empirical algorithm to derive DOC concentrations from the ratio of Rrs(412)/Rrs(488) and tested it with independent datasets. In this study, we demonstrate the ability to estimate DOC using remotely sensed optical observations in turbid coastal waters.

  4. Diurnal variations in, and influences on, concentrations of particulate and dissolved arsenic and metals in the mildly alkaline Wallkill River, New Jersey, USA

    USGS Publications Warehouse

    Barringer, J.L.; Wilson, T.P.; Szabo, Z.; Bonin, J.L.; Fischer, J.M.; Smith, N.P.

    2008-01-01

    Diurnal variations in particulate and dissolved As and metal concentrations were observed in mildly alkaline water from a wetlands site on the Wallkill River in northwestern New Jersey. The site, underlain by glacial sediments over dolomite bedrock, is 10 km downstream from a mined area of the Franklin Marble, host to Zn ores, also As and Mn minerals. In mid-September 2005, maxima and minima in dissolved-oxygen-concentration and pH, typically caused by photosynthesis and respiration, occurred at 2000 and 0800 hours. Concentrations of dissolved As (1.52-1.95 ??g/L) peaked at dusk (2000 hours), whereas dissolved Mn and Zn concentrations (76.5-96.9 and 8.55-12.8 ??g/L, respectively) were lowest at dusk and peaked at 1000 hours. These opposing cycles probably reflect sorption and desorption of As (an anion), and Mn and Zn (cations) as pH varied throughout the 24-h period. Doubly-peaked cycles of B, Cl, SO4, and nutrients also were observed; these may result from upstream discharges of septic-system effluent. Both recoverable amd particulate Al, Fe, Mn, and Zn concentrations peaked between 0200 and 0600 hours. The particulate metals cycle, with perturbations at 0400 hours, may be influenced by biological activity. ?? 2007 Springer-Verlag.

  5. Diurnal variations in, and influences on, concentrations of particulate and dissolved arsenic and metals in the mildly alkaline Wallkill River, New Jersey, USA

    NASA Astrophysics Data System (ADS)

    Barringer, Julia L.; Wilson, Timothy P.; Szabo, Zoltan; Bonin, Jennifer L.; Fischer, Jeffrey M.; Smith, Nicholas P.

    2008-01-01

    Diurnal variations in particulate and dissolved As and metal concentrations were observed in mildly alkaline water from a wetlands site on the Wallkill River in northwestern New Jersey. The site, underlain by glacial sediments over dolomite bedrock, is 10 km downstream from a mined area of the Franklin Marble, host to Zn ores, also As and Mn minerals. In mid-September 2005, maxima and minima in dissolved-oxygen-concentration and pH, typically caused by photosynthesis and respiration, occurred at 2000 and 0800 hours. Concentrations of dissolved As (1.52-1.95 μg/L) peaked at dusk (2000 hours), whereas dissolved Mn and Zn concentrations (76.5-96.9 and 8.55-12.8 μg/L, respectively) were lowest at dusk and peaked at 1000 hours. These opposing cycles probably reflect sorption and desorption of As (an anion), and Mn and Zn (cations) as pH varied throughout the 24-h period. Doubly-peaked cycles of B, Cl, SO4, and nutrients also were observed; these may result from upstream discharges of septic-system effluent. Both recoverable amd particulate Al, Fe, Mn, and Zn concentrations peaked between 0200 and 0600 hours. The particulate metals cycle, with perturbations at 0400 hours, may be influenced by biological activity.

  6. Rapid depletion of dissolved oxygen in 96-well microtiter plate Staphylococcus epidermidis biofilm assays promotes biofilm development and is influenced by inoculum cell concentration.

    PubMed

    Cotter, John J; O'Gara, James P; Casey, Eoin

    2009-08-01

    Biofilm-related research using 96-well microtiter plates involves static incubation of plates indiscriminate of environmental conditions, making oxygen availability an important variable which has not been considered to date. By directly measuring dissolved oxygen concentration over time we report here that dissolved oxygen is rapidly consumed in Staphylococcus epidermidis biofilm cultures grown in 96-well plates irrespective of the oxygen concentration in the gaseous environment in which the plates are incubated. These data indicate that depletion of dissolved oxygen during growth of bacterial biofilm cultures in 96-well plates may significantly influence biofilm production. Furthermore higher inoculum cell concentrations are associated with more rapid consumption of dissolved oxygen and higher levels of S. epidermidis biofilm production. Our data reveal that oxygen depletion during bacterial growth in 96-well plates may significantly influence biofilm production and should be considered in the interpretation of experimental data using this biofilm model.

  7. Numerical Simulation of the Effect about Groundwater Level Fluctuation on the Concentration of BTEX Dissolved into Source Zone

    NASA Astrophysics Data System (ADS)

    Sun, Liqun; Chen, Yudao; Jiang, Lingzhi; Cheng, Yaping

    2018-01-01

    The water level fluctuation of groundwater will affect the BTEX dissolution in the fuel leakage source zone. In order to study the effect, a leakage test of gasoline was performed in the sand-tank model in the laboratory, and the concentrations of BTEX along with water level were monitored over a long period. Combined with VISUAL MODFLOW software, RT3D module was used to simulate the concentrations of BTEX, and mass flux method was used to evaluate the effects of water level fluctuation on the BTEX dissolution. The results indicate that water level fluctuation can significantly increase the concentration of BTEX dissolved in the leakage source zone. The dissolved amount of BTEX can reach up to 2.4 times under the water level fluctuation condition. The method of numerical simulation combined with mass flux calculation can be used to evaluate the effect of water level fluctuation on BTEX dissolution.

  8. Mercury, monomethyl mercury, and dissolved organic carbon concentrations in surface water entering and exiting constructed wetlands treated with metal-based coagulants, Twitchell Island, California

    USGS Publications Warehouse

    Stumpner, Elizabeth B.; Kraus, Tamara E.C.; Fleck, Jacob A.; Hansen, Angela M.; Bachand, Sandra M.; Horwath, William R.; DeWild, John F.; Krabbenhoft, David P.; Bachand, Philip A.M.

    2015-09-02

    Following coagulation, but prior to passage through the wetland cells, coagulation treatments transferred dissolved mercury and carbon to the particulate fraction relative to untreated source water: at the wetland cell inlets, the coagulation treatments decreased concentrations of filtered total mercury by 59–76 percent, filtered monomethyl mercury by 40–70 percent, and dissolved organic carbon by 65–86 percent. Passage through the wetland cells decreased the particulate fraction of mercury in wetland cells that received coagulant-treated water. Changes in total mercury, monomethyl mercury, and dissolved organic carbon concentrations resulting from wetland passage varied both by treatment and season. Despite increased monomethyl mercury in the filtered fraction during wetland passage between March and August, the coagulation-wetland systems generally decreased total mercury (filtered plus particulate) and monomethyl mercury (filtered plus particulate) concentrations relative to source water. Coagulation—either alone or in association with constructed wetlands—could be an effective way to decrease concentrations of mercury and dissolved organic carbon in surface water as well as the bioavailability of mercury in the Sacramento–San Joaquin Delta.

  9. Using polyacrylate-coated SPME fibers to quantify sorption of polar and ionic organic contaminants to dissolved organic carbon.

    PubMed

    Haftka, Joris J-H; Scherpenisse, Peter; Jonker, Michiel T O; Hermens, Joop L M

    2013-05-07

    A passive sampling method using polyacrylate-coated solid-phase microextraction (SPME) fibers was applied to determine sorption of polar and ionic organic contaminants to dissolved organic carbon (DOC). The tested contaminants included pharmaceuticals, industrial chemicals, hormones, and pesticides and represented neutral, anionic, and cationic structures. Prior to the passive sampler application, sorption of the chemicals to the fibers was characterized. This was needed in order to accurately translate concentrations measured in fibers to freely dissolved aqueous concentrations during the sorption tests with DOC. Sorption isotherms of neutral compounds to the fiber were linear, whereas isotherms of basic chemicals covered a nonlinear and a linear range. Sorption of acidic and basic compounds to the fiber was pH-dependent and was dominated by sorption of the neutral sorbate species. Fiber- and DOC-water partition coefficients of neutral compounds were both linearly related to octanol-water partition coefficients (log Kow). The results of this study show that polyacrylate fibers can be used to quantify sorption to DOC of neutral and ionic contaminants, having multiple functional groups and spanning a wide hydrophobicity range (log Kow = 2.5-7.5).

  10. An in situ method to quantitatively determine dissolved free drug concentrations in vitro in the presence of polymer excipients using pulsatile microdialysis (PMD).

    PubMed

    Vejani, Charchil; Bellantone, Robert A

    2015-12-30

    In drug formulations containing polymer excipients, the effects of the polymer on the dissolved free drug concentration and resulting dissolution or release can be important, especially for poorly soluble drugs. In this study, an in vitro method based on pulsatile microdialysis (PMD) was developed to quantitatively determine dissolved free concentrations of drugs in the presence of polymers in aqueous media in situ (e.g., in place within the system being characterized). Formulations were made by dissolving various ratios of the drug griseofulvin and polymer PVP K30 in water and allowing the mix to equilibrate. A PMD probe was immersed in each mixture and the dissolved free drug concentrations were determined in the PMD samples. The experimental procedure and the equations used for data analysis are presented. To assess the consistency of data, a binding model was fit to the data obtained using PMD by calculating the dissolved free drug fraction fD for each drug-polymer ratio in solution, and obtaining the product of the binding stoichiometry and binding constant (νK per mole of polymer) from the slope of a plot of (1-fD)/fD vs. the molar polymer concentration. For comparison, equilibrium binding experiments were also performed at 23C, and the determined value of νK was similar to the value found using PMD. Experiments were performed at three temperatures, and a plot of ln (νK) vs. 1/T was linear and a binding enthalpy of -110.9±4.4J/mol of monomer was calculated from its slope. It was concluded that PMD can be used to determine the dissolved free drug concentrations in situ, which allows characterization of the drug-polymer interaction, even for low drug concentrations. This information may be important in modeling the dissolution or release of drugs from formulations containing polymers. Copyright © 2015 Elsevier B.V. All rights reserved.

  11. Effect of water hardness and dissolved-solid concentration on hatching success and egg size in bighead carp

    USGS Publications Warehouse

    Chapman, Duane C.; Deters, Joseph E.

    2009-01-01

    Bighead carp Hypophthalmichthys nobilis is an Asian species that has been introduced to the United States and is regarded as a highly undesirable invader. Soft water has been said to cause the bursting of Asian carp eggs and thus has been suggested as a factor that would limit the spread of this species. To evaluate this, we subjected fertilized eggs of bighead carp to waters with a wide range of hardness and dissolved-solid concentrations. Hatching rate and egg size were not significantly affected by the different water qualities. These results, combined with the low hardness (28–84 mg/L) of the Yangtze River (the primary natal habitat of Hypophthalmichthys spp.), suggest that managers and those performing risk assessments for the establishment of Hypophthalmichthys spp. should be cautious about treating low hardness and dissolved-solid concentrations as limiting factors.

  12. Influences of observation method, season, soil depth, land use and management practice on soil dissolvable organic carbon concentrations: A meta-analysis.

    PubMed

    Li, Siqi; Zheng, Xunhua; Liu, Chunyan; Yao, Zhisheng; Zhang, Wei; Han, Shenghui

    2018-08-01

    Quantifications of soil dissolvable organic carbon concentrations, together with other relevant variables, are needed to understand the carbon biogeochemistry of terrestrial ecosystems. Soil dissolvable organic carbon can generally be grouped into two incomparable categories. One is soil extractable organic carbon (EOC), which is measured by extracting with an aqueous extractant (distilled water or a salt solution). The other is soil dissolved organic carbon (DOC), which is measured by sampling soil water using tension-free lysimeters or tension samplers. The influences of observation methods, natural factors and management practices on the measured concentrations, which ranged from 2.5-3970 (mean: 69) mg kg -1 of EOC and 0.4-200 (mean: 12) mg L -1 of DOC, were investigated through a meta-analysis. The observation methods (e.g., extractant, extractant-to-soil ratio and pre-treatment) had significant effects on EOC concentrations. The most significant divergence (approximately 109%) occurred especially at the extractant of potassium sulfate (K 2 SO 4 ) solutions compared to distilled water. As EOC concentrations were significantly different (approximately 47%) between non-cultivated and cultivated soils, they were more suitable than DOC concentrations for assessing the influence of land use on soil dissolvable organic carbon levels. While season did not significantly affect EOC concentrations, DOC concentrations showed significant differences (approximately 50%) in summer and autumn compared to spring. For management practices, applications of crop residues and nitrogen fertilizers showed positive effects (approximately 23% to 91%) on soil EOC concentrations, while tillage displayed negative effects (approximately -17%), compared to no straw, no nitrogen fertilizer and no tillage. Compared to no nitrogen, applications of synthetic nitrogen also appeared to significantly enhance DOC concentrations (approximately 32%). However, further studies are needed in the future

  13. Characterization of the structure, clean-sand percentage, dissolved-solids concentrations, and estimated quantity of groundwater in the Upper Cretaceous Nacatoch Sand and Tokio Formation, Arkansas

    USGS Publications Warehouse

    Gillip, Jonathan A.

    2014-01-01

    The West Gulf Coastal Plain, Mississippi embayment, and underlying Cretaceous aquifers are rich in water resources; however, large parts of the aquifers are largely unusable because of large concentrations of dissolved solids. Cretaceous aquifers are known to have large concentrations of salinity in some parts of Arkansas. The Nacatoch Sand and the Tokio Formation of Upper Cretaceous age were chosen for investigation because these aquifers produce groundwater to wells near their outcrops and have large salinity concentrations away from their outcrop areas. Previous investigations have indicated that dissolved-solids concentrations of groundwater within the Nacatoch Sand, 2–20 miles downdip from the outcrop, render the groundwater as unusable for purposes requiring freshwater. Groundwater within the Tokio Formation also exhibits large concentrations of dissolved solids downdip. Water-quality data showing elevated dissolved-solids concentrations are limited for these Cretaceous aquifers because other shallower aquifers are used for water supply. Although not suitable for many uses, large, unused amounts of saline groundwater are present in these aquifers. Historical borehole geophysical logs were used to determine the geologic and hydrogeologic properties of these Cretaceous aquifers, as well as the quality of the groundwater within the aquifers. Based on the interpretation of borehole geophysical logs, in Arkansas, the altitude of the top of the Nacatoch Sand ranges from more than 200 to less than -4,000 feet; the structural high occurs in the outcrop area and the structural low occurs in southeastern Arkansas near the Desha Basin structural feature. The thickness of the Nacatoch Sand ranges from 0 to over 550 feet. The minimum thickness occurs where the formation pinches out in the outcrop area, and the maximum thickness occurs in the southwestern corner of Arkansas. Other areas of large thickness include the area of the Desha Basin structural feature in

  14. Analysis of dissolved organic carbon concentration and 13C isotopic signature by TOC-IRMS - assessment of analytical performance

    NASA Astrophysics Data System (ADS)

    Kirkels, Frédérique; Cerli, Chiara; Federherr, Eugen; Kalbitz, Karsten

    2013-04-01

    Stable carbon isotopes provide a powerful tool to assess carbon pools and their dynamics. Dissolved organic carbon (DOC) has been recognized to play an important role in ecosystem functioning and carbon cycling and has therefore gained increased research interest. However, direct measurement of 13C isotopic signature of carbon in the dissolved phase is technically challenging particularly using high temperature combustion. Until recently, mainly custom-made systems existed which were modified for coupling of TOC instruments with IRMS for simultaneous assessment of C content and isotopic signature. The variety of coupled systems showed differences in their analytical performances. For analysis of DOC high temperature combustion is recognized as best performing method, owing to its high efficiency of conversion to CO2 also for highly refractory components (e.g. humic, fulvic acids) present in DOC and soil extracts. Therefore, we tested high temperature combustion TOC coupled to IRMS (developed by Elementar Group) for bulk measurements of DOC concentration and 13C signature. The instruments are coupled via an Interface to exchange the carrier gas from O2 to He and to concentrate the derived CO2 for the isotope measurement. Analytical performance of the system was assessed for a variety of organic compounds characterized by different stability and complexity, including humic acid and DOM. We tested injection volumes between 0.2-3 ml, thereby enabling measurement of broad concentration ranges. With an injection volume of 0.5 ml (n=3, preceded by 1 discarded injection), DOC and 13C signatures for concentrations between 5-150 mg C/L were analyzed with high precision (standard deviation (SD) predominantly <0.1‰), good accuracy and linearity (overall SD <0.9‰). For the same settings, slightly higher variation in precision was observed among the lower concentration range and depending upon specific system conditions. Differences in 13C signatures of about 50‰ among

  15. An improved biofilter to control the dissolved organic nitrogen concentration during drinking water treatment.

    PubMed

    Zhang, Huining; Gu, Li; Liu, Bing; Gan, Huihui; Zhang, Kefeng; Jin, Huixia; Yu, Xin

    2016-09-01

    Dissolved organic nitrogen (DON) is a key precursor of numerous disinfection by-products (DBPs), especially nitrogenous DBPs (N-DBPs) formed during disinfection in drinking water treatment. To effectively control DBPs, reduction of the DON concentration before the disinfection process is critical. Traditional biofilters can increase the DON concentration in the effluent, so an improved biofilter is needed. In this study, an improved biofilter was set up with two-layer columns using activated carbon and quartz sand under different influent patterns. Compared with the single-layer filter, the two-layer biofilter controlled the DON concentration more efficiently. The two-point influent biofilter controlled the DON concentration more effectively than the single-point influent biofilter. The improved biofilter resulted in an environment (including matrix, DO, and pH) suitable for microbial growth. Along the depth of the biofilter column, the environment affected the microbial biomass and microbial activity and thus affected the DON concentration.

  16. Assessing the utility of dissolved organic matter photoreactivity as a predictor of in situ methylmercury concentration.

    PubMed

    Klapstein, Sara J; Ziegler, Susan E; Risk, David A; O'Driscoll, Nelson J

    2018-06-01

    Methylmercury (MeHg) bioaccumulation is a growing concern in ecosystems worldwide. The absorption of solar radiation by dissolved organic matter (DOM) and other photoreactive ligands can convert MeHg into less toxic forms of mercury through photodemethylation. In this study, spectral changes and photoreactivity of DOM were measured to assess the potential to control photoreactions and predict in situ MeHg concentration. Water samples collected from a series of lakes in southwestern Nova Scotia in June, August, and September were exposed to controlled ultraviolet-A (UV-A) radiation for up to 24hr. Dissolved organic matter photoreactivity, measured as the loss of absorbance at 350nm at constant UV-A irradiation, was positively dependent on the initial DOM concentration in lake waters (r 2 =0.94). This relationship was consistent over time with both DOM concentration and photoreactivity increasing from summer into fall across lakes. Lake in situ MeHg concentration was positively correlated with DOM concentration and likely catchment transport in June (r=0.77) but not the other sampling months. Despite a consistent seasonal variation in both DOM and Fe, and their respective correlations with MeHg, no discernable seasonal trend in MeHg was observed. However, a 3-year dataset from the 6 study lakes revealed a positive correlation between DOM concentration and both Fe (r=0.91) and MeHg concentrations (r=0.51) suggesting a more dominant landscape mobility control on MeHg. The DOM-MeHg relationships observed in these lakes highlights the need to examine DOM photoreactivity controls on MeHg transport and availability in natural waters particularly given future climate perturbations. Copyright © 2018. Published by Elsevier B.V.

  17. Fate of polychlorinated biphenyls in a contaminated lake ecosystem: combining equilibrium passive sampling of sediment and water with total concentration measurements of biota.

    PubMed

    Mäenpää, Kimmo; Leppänen, Matti T; Figueiredo, Kaisa; Mayer, Philipp; Gilbert, Dorothea; Jahnke, Annika; Gil-Allué, Carmen; Akkanen, Jarkko; Nybom, Inna; Herve, Sirpa

    2015-11-01

    Equilibrium sampling devices can be applied to study and monitor the exposure and fate of hydrophobic organic chemicals on a thermodynamic basis. They can be used to determine freely dissolved concentrations and chemical activity ratios and to predict equilibrium partitioning concentrations of hydrophobic organic chemicals in biota lipids. The authors' aim was to assess the equilibrium status of polychlorinated biphenyls (PCBs) in a contaminated lake ecosystem and along its discharge course using equilibrium sampling devices for measurements in sediment and water and by also analyzing biota. The authors used equilibrium sampling devices (silicone rubber and polyethylene [PE]) to determine freely dissolved concentrations and chemical activities of PCBs in the water column and sediment porewater and calculated for both phases the corresponding equilibrium concentrations and chemical activities in model lipids. Overall, the studied ecosystem appeared to be in disequilibrium for the studied phases: sediment, water, and biota. Chemical activities of PCBs were higher in sediment than in water, which implies that the sediment functioned as a partitioning source of PCBs and that net diffusion occurred from the sediment to the water column. Measured lipid-normalized PCB concentrations in biota were generally below equilibrium lipid concentrations relative to the sediment (CLip ⇌Sed ) or water (CLip ⇌W ), indicating that PCB levels in the organisms were below the maximum partitioning levels. The present study shows the application versatility of equilibrium sampling devices in the field and facilitates a thermodynamic understanding of exposure and fate of PCBs in a contaminated lake and its discharge course. © 2015 SETAC.

  18. Dissolved organic carbon concentration controls benthic primary production: results from in situ chambers in north-temperate lakes

    USGS Publications Warehouse

    Godwin, Sean C.; Jones, Stuart E.; Weidel, Brian C.; Solomon, Christopher T.

    2014-01-01

    We evaluated several potential drivers of primary production by benthic algae (periphyton) in north-temperate lakes. We used continuous dissolved oxygen measurements from in situ benthic chambers to quantify primary production by periphyton at multiple depths across 11 lakes encompassing a broad range of dissolved organic carbon (DOC) and total phosphorous (TP) concentrations. Light-use efficiency (primary production per unit incident light) was inversely related to average light availability (% of surface light) in 7 of the 11 study lakes, indicating that benthic algal assemblages exhibit photoadaptation, likely through physiological or compositional changes. DOC alone explained 86% of the variability in log-transformed whole-lake benthic production rates. TP was not an important driver of benthic production via its effects on nutrient and light availability. This result is contrary to studies in other systems, but may be common in relatively pristine north-temperate lakes. Our simple empirical model may allow for the prediction of whole-lake benthic primary production from easily obtained measurements of DOC concentration.

  19. Weathering and evaporation controls on dissolved uranium concentrations in groundwater - A case study from northern Burundi.

    PubMed

    Post, V E A; Vassolo, S I; Tiberghien, C; Baranyikwa, D; Miburo, D

    2017-12-31

    The potential use of groundwater for potable water supply can be severely compromised by natural contaminants such as uranium. The environmental mobility of uranium depends on a suite of factors including aquifer lithology, redox conditions, complexing agents, and hydrological processes. Uranium concentrations of up to 734μg/L are found in groundwater in northern Burundi, and the objective of the present study was to identify the causes for these elevated concentrations. Based on a comprehensive data set of groundwater chemistry, geology, and hydrological measurements, it was found that the highest dissolved uranium concentrations in groundwater occur near the shores of Lake Tshohoha South and other smaller lakes nearby. A model is proposed in which weathering and evapotranspiration during groundwater recharge, flow and discharge exert the dominant controls on the groundwater chemical composition. Results of PHREEQC simulations quantitatively confirm this conceptual model and show that uranium mobilization followed by evapo-concentration is the most likely explanation for the high dissolved uranium concentrations observed. The uranium source is the granitic sand, which was found to have a mean elemental uranium content of 14ppm, but the exact mobilization process could not be established. Uranium concentrations may further be controlled by adsorption, especially where calcium-uranyl‑carbonate complexes are present. Water and uranium mass balance calculations for Lake Tshohoha South are consistent with the inferred fluxes and show that high‑uranium groundwater represents only a minor fraction of the overall water input to the lake. These findings highlight that the evaporation effects that cause radionuclide concentrations to rise to harmful levels in groundwater discharge areas are not only confined to arid regions, and that this should be considered when selecting suitable locations for water supply wells. Copyright © 2017 Elsevier B.V. All rights reserved.

  20. Freely oriented portable superconducting magnet

    DOEpatents

    Schmierer, Eric N [Los Alamos, NM; Prenger, F Coyne [Los Alamos, NM; Hill, Dallas D [Los Alamos, NM

    2010-01-12

    A freely oriented portable superconducting magnet is disclosed. Coolant is supplied to the superconducting magnet from a repository separate from the magnet, enabling portability of the magnet. A plurality of support assemblies structurally anchor and thermally isolate the magnet within a thermal shield. A plurality of support assemblies structurally anchor and thermally isolate the thermal shield within a vacuum vessel. The support assemblies restrain movement of the magnet resulting from energizing and cooldown, as well as from changes in orientation, enabling the magnet to be freely orientable.

  1. Seasonal changes in concentrations of dissolved pesticides and organic carbon in the Sacramento-San Joaquin delta, California, 1994-1996

    USGS Publications Warehouse

    Orlando, James L.; Kuivila, Kathryn

    2006-01-01

    The Sacramento-San Joaquin Delta (Delta) of California is an ecologically rich and hydrologically complex region that receives runoff from nearly one-quarter of the state. Water-quality studies of surface water in the region have found dissolved pesticides in winter storm runoff at concentrations toxic to some aquatic invertebrates. However, scientists have little information on pesticide concentrations in the Delta on a seasonal timescale or the importance of pesticide contributions from within-Delta sources. Consequently, the U.S. Geological Survey conducted a study from 1994 to 1996 during which water samples were collected seasonally from 31 sites located within the Delta and on major tributaries to the Delta. Water samples were analyzed for 20 current-use pesticides and dissolved organic carbon. During the study, 11 current-use pesticides were detected; maximum concentrations ranging from 17 ng/L (for trifluralin) to 1,160 ng/L (for metolachlor). The highest concentrations of five pesticides (carbaryl, carbofuran, metolachlor, molinate, and simazine) were greater than 900 ng/L. The greatest number of pesticides was detected in the summer of 1994, whereas the least number were detected in the winter of 1994. The herbicides metolachlor and simazine were the most frequently detected pesticides and were detected in five of the six sampling seasons. The herbicides molinate and EPTC were detected only during the three summer sampling seasons. A comparison of pesticides detected during the spring and summer of 1995 showed some seasonal variability. Comparison of the three summer seasons sampled showed that a larger number of pesticides were detected, and with generally higher maximum concentrations, in 1994 than in 1995 or 1996. Dissolved organic carbon (DOC) concentrations ranged, over the course of the study, from 1.4 mg/L to 10.4 mg/L, and had a median concentration of 3.8 mg/L. On a seasonal basis, the lowest maximum DOC concentrations occurred during the summer

  2. Strategies of Nitrosomonas europaea 19718 to counter low dissolved oxygen and high nitrite concentrations.

    PubMed

    Yu, Ran; Chandran, Kartik

    2010-03-04

    Nitrosomonas europaea is a widely studied chemolithoautotrophic ammonia oxidizing bacterium. While significant work exists on the ammonia oxidation pathway of N. europaea, its responses to factors such as dissolved oxygen limitation or sufficiency or exposure to high nitrite concentrations, particularly at the functional gene transcription level are relatively sparse. The principal goal of this study was to investigate responses at the whole-cell activity and gene transcript levels in N. europaea 19718 batch cultures, which were cultivated at different dissolved oxygen and nitrite concentrations. Transcription of genes coding for principal metabolic pathways including ammonia oxidation (amoA), hydroxylamine oxidation (hao), nitrite reduction (nirK) and nitric oxide reduction (norB) were quantitatively measured during batch growth, at a range of DO concentrations (0.5, 1.5 and 3.0 mg O2/L). Measurements were also conducted during growth at 1.5 mg O2/L in the presence of 280 mg-N/L of externally added nitrite. Several wide ranging responses to DO limitation and nitrite toxicity were observed in N. europaea batch cultures. In contrast to our initial hypothesis, exponential phase mRNA concentrations of both amoA and hao increased with decreasing DO concentrations, suggesting a mechanism to metabolize ammonia and hydroxylamine more effectively under DO limitation. Batch growth in the presence of 280 mg nitrite-N/L resulted in elevated exponential phase nirK and norB mRNA concentrations, potentially to promote utilization of nitrite as an electron acceptor and to detoxify nitrite. This response was in keeping with our initial hypothesis and congruent with similar responses in heterotrophic denitrifying bacteria. Stationary phase responses were distinct from exponential phase responses in most cases, suggesting a strong impact of ammonia availability and metabolism on responses to DO limitation and nitrite toxicity. In general, whole-cell responses to DO limitation or

  3. Temporal Dynamics of Dissolved Oxygen Concentrations in the Hyporheic Zone.

    NASA Astrophysics Data System (ADS)

    Reeder, W. J.; Quick, A. M.; Farrell, T. B.; Benner, S. G.; Feris, K. P.; Tonina, D.

    2016-12-01

    Dissolved oxygen (DO) concentration profiles and DO consumption rates are primary indicators of the redox state of porewaters in the hyporheic zone (HZ). Previous studies (mostly numeric) of reactive solute transport, in the HZ, are steady state and give a fixed, in time, view of the biogeochemical activity and redox state of the HZ. Through the use of a novel, multichannel fiber optic DO measurement system and a robotic surface probe system in a large flume experiment, we have been able to track DO concentration, in the HZ, over time and at high spatial and temporal resolutions never achieved before. Our research shows that in carbon-limited systems (i.e., ones in which organic carbon replenishment is largely episodic), DO concentration profiles and consumption rates will vary as a function of time. As the most readily available organic carbon is consumed, (first near the bed surface/water interface) respiration rates, in that area, will drop and DO will be transported deeper into the HZ. Over time, and lacking either an external source of bioavailable carbon or an alternate electron donor substrate, microbial metabolic activity will slow substantially and the majority of the HZ will be rendered oxic. Hyporheic fluxes affect the time scale of biological reactions resulting in faster growth of the aerobic zone in high-flux systems. While this temporal variability can result in a multitude of DO consumption curves (DO vs. residence time), the careful application of dimensional analysis can collapse the consumption curves to a single characteristic curve that accounts for a wide range of morphology and reactivity.

  4. Deriving sediment Interstitial Water Remediation Goals (IWRGs) for the protection of benthic organisms from direct toxicity

    EPA Science Inventory

    Background/Objectives. Passive sampling is becoming a frequently used measurement technique at Superfund sites with contaminated sediments. Passive sampling measures the concentrations of freely dissolved chemicals (Cfrees) in the sediment interstitial water. The freely dissol...

  5. [Effects of nitrogen addition and elevated CO2 concentration on soil dissolved organic carbon and nitrogen in rhizosphere and non-rhizosphere of Bothriochloa ischaemum].

    PubMed

    Xiao, Lie; Liu, Guo Bin; Li, Peng; Xue, Sha

    2017-01-01

    A pot experiment was conducted to study soil dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) in the rhizosphere and non-rhizosphere of Bothriochloa ischaemum in loess hilly-gully region under the different treatments of CO 2 concentrations (400 and 800 μmol·mol -1 ) and nitrogen addition (0, 2.5, 5.0 g N·m -2 ·a -1 ). The results showed that eleva-ted CO 2 treatments had no significant effect on the contents of DOC, dissolved total nitrogen (DTN), DON, dissolved ammonium nitrogen (NH 4 + -N) and dissolved nitrate nitrogen (NO 3 - -N) in the soil of rhizosphere and non-rhizosphere of B. ischaemum. The contents of DTN, DON, and NO 3 - -N in the rhizosphere soil were significantly increased with the nitrogen application and the similar results of DTN and NO 3 - -N also were observed in the non-rhizosphere of B. ischaemum. Nitrogen application significantly decreased DOC/DON in the rhizosphere of B. ischaemum. The contents of DTN, NO 3 - -N and DON in the soil of rhizosphere were significantly lower than that in the non-rhizosphere soil, and DOC/DON was significantly higher in the rhizosphere soil than that in the non-rhizosphere soil. It indicated that short-term elevated CO 2 concentration had no significant influence on the contents of soil dissolved organic carbon and nitrogen. Simulated nitrogen deposition, to some extent, increased the content of soil dissolved nitrogen, but it was still insufficient to meet the demand of dissolved nitrogen for plant growing.

  6. Effects of reduced dissolved oxygen concentrations on physiology and fluorescence of hermatypic corals and benthic algae

    PubMed Central

    Smith, Jennifer E.; Thompson, Melissa

    2014-01-01

    While shifts from coral to seaweed dominance have become increasingly common on coral reefs and factors triggering these shifts successively identified, the primary mechanisms involved in coral-algae interactions remain unclear. Amongst various potential mechanisms, algal exudates can mediate increases in microbial activity, leading to localized hypoxic conditions which may cause coral mortality in the direct vicinity. Most of the processes likely causing such algal exudate induced coral mortality have been quantified (e.g., labile organic matter release, increased microbial metabolism, decreased dissolved oxygen availability), yet little is known about how reduced dissolved oxygen concentrations affect competitive dynamics between seaweeds and corals. The goals of this study were to investigate the effects of different levels of oxygen including hypoxic conditions on a common hermatypic coral Acropora yongei and the common green alga Bryopsis pennata. Specifically, we examined how photosynthetic oxygen production, dark and daylight adapted quantum yield, intensity and anatomical distribution of the coral innate fluorescence, and visual estimates of health varied with differing background oxygen conditions. Our results showed that the algae were significantly more tolerant to extremely low oxygen concentrations (2–4 mg L−1) than corals. Furthermore corals could tolerate reduced oxygen concentrations, but only until a given threshold determined by a combination of exposure time and concentration. Exceeding this threshold led to rapid loss of coral tissue and mortality. This study concludes that hypoxia may indeed play a significant role, or in some cases may even be the main cause, for coral tissue loss during coral-algae interaction processes. PMID:24482757

  7. Effects of reduced dissolved oxygen concentrations on physiology and fluorescence of hermatypic corals and benthic algae.

    PubMed

    Haas, Andreas F; Smith, Jennifer E; Thompson, Melissa; Deheyn, Dimitri D

    2014-01-01

    While shifts from coral to seaweed dominance have become increasingly common on coral reefs and factors triggering these shifts successively identified, the primary mechanisms involved in coral-algae interactions remain unclear. Amongst various potential mechanisms, algal exudates can mediate increases in microbial activity, leading to localized hypoxic conditions which may cause coral mortality in the direct vicinity. Most of the processes likely causing such algal exudate induced coral mortality have been quantified (e.g., labile organic matter release, increased microbial metabolism, decreased dissolved oxygen availability), yet little is known about how reduced dissolved oxygen concentrations affect competitive dynamics between seaweeds and corals. The goals of this study were to investigate the effects of different levels of oxygen including hypoxic conditions on a common hermatypic coral Acropora yongei and the common green alga Bryopsis pennata. Specifically, we examined how photosynthetic oxygen production, dark and daylight adapted quantum yield, intensity and anatomical distribution of the coral innate fluorescence, and visual estimates of health varied with differing background oxygen conditions. Our results showed that the algae were significantly more tolerant to extremely low oxygen concentrations (2-4 mg L(-1)) than corals. Furthermore corals could tolerate reduced oxygen concentrations, but only until a given threshold determined by a combination of exposure time and concentration. Exceeding this threshold led to rapid loss of coral tissue and mortality. This study concludes that hypoxia may indeed play a significant role, or in some cases may even be the main cause, for coral tissue loss during coral-algae interaction processes.

  8. Dissolved carbon dioxide and oxygen concentrations in purge of vacuum-packaged pork chops and the relationship to shelf life and models for estimating microbial populations.

    PubMed

    Adams, K R; Niebuhr, S E; Dickson, J S

    2015-12-01

    The objectives of this study were to determine the dissolved CO2 and O2 concentrations in the purge of vacuum-packaged pork chops over a 60 day storage period, and to elucidate the relationship of dissolved CO2 and O2 to the microbial populations and shelf life. As the populations of spoilage bacteria increased, the dissolved CO2 increased and the dissolved O2 decreased in the purge. Lactic acid bacteria dominated the spoilage microflora, followed by Enterobacteriaceae and Brochothrix thermosphacta. The surface pH decreased to 5.4 due to carbonic acid and lactic acid production before rising to 5.7 due to ammonia production. A mathematical model was developed which estimated microbial populations based on dissolved CO2 concentrations. Scanning electron microscope images were also taken of the packaging film to observe the biofilm development. The SEM images revealed a two-layer biofilm on the packaging film that was the result of the tri-phase growth environment. Copyright © 2015 Elsevier Ltd. All rights reserved.

  9. Comparative production of channel catfish and channel x blue hybrid catfish subjected to two minimum dissolved oxygen concentrations

    USDA-ARS?s Scientific Manuscript database

    The effect of daily minimum dissolved oxygen concentration on growth and yield (kg/ha) of the channel catfish (Ictalurus punctatus) and the channel x blue hybrid catfish (I. punctatus female x I. furcatus male), which shared the Jubilee strain of channel catfish as the maternal parent, was evaluated...

  10. Sources, transformations, and hydrological processes that control stream nitrate and dissolved organic matter concentrations during snowmelt in an upland forest

    USGS Publications Warehouse

    Sebestyen, Stephen D.; Boyer, Elizabeth W.; Shanley, James B.; Kendall, Carol; Doctor, Daniel H.; Aiken, George R.; Ohte, Nobuhito

    2008-01-01

    We explored catchment processes that control stream nutrient concentrations at an upland forest in northeastern Vermont, USA, where inputs of nitrogen via atmospheric deposition are among the highest in the nation and affect ecosystem functioning. We traced sources of water, nitrate, and dissolved organic matter (DOM) using stream water samples collected at high frequency during spring snowmelt. Hydrochemistry, isotopic tracers, and end‐member mixing analyses suggested the timing, sources, and source areas from which water and nutrients entered the stream. Although stream‐dissolved organic carbon (DOC) and dissolved organic nitrogen (DON) both originated from leaching of soluble organic matter, flushing responses between these two DOM components varied because of dynamic shifts of hydrological flow paths and sources that supply the highest concentrations of DOC and DON. High concentrations of stream water nitrate originated from atmospheric sources as well as nitrified sources from catchment soils. We detected nitrification in surficial soils during late snowmelt which affected the nitrate supply that was available to be transported to streams. However, isotopic tracers showed that the majority of nitrate in upslope surficial soil waters after the onset of snowmelt originated from atmospheric sources. A fraction of the atmospheric nitrogen was directly delivered to the stream, and this finding highlights the importance of quick flow pathways during snowmelt events. These findings indicate that interactions among sources, transformations, and hydrologic transport processes must be deciphered to understand why concentrations vary over time and over space as well as to elucidate the direct effects of human activities on nutrient dynamics in upland forest streams.

  11. Effect of nitrate concentration on filamentous bulking under low level of dissolved oxygen in an airlift inner circular anoxic-aerobic incorporate reactor.

    PubMed

    Su, Yiming; Zhang, Yalei; Zhou, Xuefei; Jiang, Ming

    2013-09-01

    This laboratory research investigated a possible cause of filamentous bulking under low level of dissolved oxygen conditions (dissolved oxygen value in aerobic zone maintained between 0.6-0.8 mg O2/L) in an airlift inner-circular anoxic-aerobic reactor. During the operating period, it was observed that low nitrate concentrations affected sludge volume index significantly. Unlike the existing hypothesis, the batch tests indicated that filamentous bacteria (mainly Thiothrix sp.) could store nitrate temporarily under carbon restricted conditions. When nitrate concentration was below 4 mg/L, low levels of carbon substrates and dissolved oxygen in the aerobic zone stimulated the nitrate-storing capacity of filaments. When filamentous bacteria riched in nitrate reached the anoxic zone, where they were exposed to high levels of carbon but limited nitrate, they underwent denitrification. However, when nonfilamentous bacteria were exposed to similar conditions, denitrification was restrained due to their intrinsic nitrate limitation. Hence, in order to avoid filamentous bulking, the nitrate concentration in the return sludge (from aerobic zone to the anoxic zone) should be above 4 mg/L, or alternatively, the nitrate load in the anoxic zone should be kept at levels above 2.7 mg NO(3-)-N/g SS.

  12. Concentration/time-dependent dissipation, partitioning and plant accumulation of hazardous current-used pesticides and 2-hydroxyatrazine in sand and soil.

    PubMed

    Neuwirthová, Natália; Bílková, Zuzana; Vašíčková, Jana; Hofman, Jakub; Bielská, Lucie

    2018-07-01

    The dissipation, partitioning dynamics and biouptake was measured for selected hazardous current-used pesticides (conazole fungicides: epoxiconazole, flusilazole, tebuconazole; prochloraz, chlorpyrifos, pendimethalin) and for a transformation product (2-hydroxyatrazine) in agricultural soil and quartz sand as representatives of a real and a worst-case scenario. Dissipation, uptake to Lactuca sativa and the freely dissolved concentration along with the organic carbon-normalized sorption coefficients (K oc ) were determined on days 12, 40, and 90 following the application of compounds at three fortification levels (0.1-1.0-10 mg/kg). Conazole fungicides showed similar dissipation patterns and were more persistent in soil than prochloraz, chlorpyrifos and pendimethalin. 2-Hydroxyatrazine showed a concentration-depended decrease in persistency in soil. Lettuce roots were shown to accumulate higher amounts than shoots where the extent of root uptake was driven by compound partitioning. This was evidenced by the ability of freely dissolved concentration (C free ) to reliably (r 2  = 0.94) predict root uptake. Concentration in leaves did not exceed the maximum residue levels (MRLs) for lettuce, which was likely given by the low root-to-shoot translocation factors (TFs) of the tested compounds varying between 0.007 and 0.14. K oc values were in the range of literature values. Sorption to soil was higher than to sand for all compounds, yet following the K oc dynamics compounds did not appear to be sequestered in soil with increasing residence time. From these results, it follows that the tested compounds may persist in soil but since they did not accumulate in lettuce above MRLs, contamination of the food web is unlikely. Copyright © 2018 Elsevier Ltd. All rights reserved.

  13. Spatial variability of dissolved phosphorous concentrations and alkaline phosphatase activity in the East China Sea

    NASA Astrophysics Data System (ADS)

    Liu, H.; Chang, J.; Ho, T.; Gong, G.

    2010-12-01

    The concentrations of dissolved inorganic phosphorus (DIP) and alkaline phosphatase activity (APA) have been determined at about 25 sampling stations in the East China Sea since 2003. The stations are mainly distributed from the Changjiang river mouth to northern Taiwan and east to the shelf break. In addition to the Changjiang discharge, we have found a specific nutrient source around a coastal site (122° 2’30’’ E, 28° 40’ N). Elevated DIP and nitrate concentrations have been constantly observed around the sampling station for 8 years, where the surface DIP concentrations are generally around 0.3 µM. The nutrient source may either originate from ground water discharge or coastal upwelling, where lower temperature has been observed in the water column around the station. In general, APA has been negatively correlated with DIP concentrations in the studies sites, with lowest APA around the high DIP station and the Changjiang river mouth.

  14. Monitoring and controlling the dissolved oxygen (DO) concentration within the high aspect ratio vessel (HARV).

    PubMed

    Saarinen, Mark A; Reece, Julie S; Arnold, Mark A; Murhammer, David W

    2003-01-01

    A probe-type oxygen sensor was developed utilizing a radioluminescent (RL)-based light source and a ruthenium-based sensing chemistry for monitoring the dissolved oxygen (DO) concentration in a modified version of the NASA-designed high aspect ratio vessel (HARV), a batch rotating wall vessel. This sensor provided the means to monitor the DO concentration in the HARV without influencing the flow pattern, thereby retaining the low shear HARV environment conducive to the formation of 3-dimensional cell aggregates. This sensor lost significant signal as a result of exposure to the first three autoclave cycles, but only minimal change in signal was observed following exposure to subsequent autoclave cycles. A new calibration model requiring only one fitted parameter was developed that accurately fit data over the entire range from 0% to 100% oxygen saturation. The ability for DO concentration control within the vessel was demonstrated by using this sensor to monitor the DO concentration inside the HARV.

  15. An empirical method for estimating instream pre-mining pH and dissolved Cu concentration in catchments with acidic drainage and ferricrete

    USGS Publications Warehouse

    Nimick, D.A.; Gurrieri, J.T.; Furniss, G.

    2009-01-01

    Methods for assessing natural background water quality of streams affected by historical mining are vigorously debated. An empirical method is proposed in which stream-specific estimation equations are generated from relationships between either pH or dissolved Cu concentration in stream water and the Fe/Cu concentration ratio in Fe-precipitates presently forming in the stream. The equations and Fe/Cu ratios for pre-mining deposits of alluvial ferricrete then were used to reconstruct estimated pre-mining longitudinal profiles for pH and dissolved Cu in three acidic streams in Montana, USA. Primary assumptions underlying the proposed method are that alluvial ferricretes and modern Fe-precipitates share a common origin, that the Cu content of Fe-precipitates remains constant during and after conversion to ferricrete, and that geochemical factors other than pH and dissolved Cu concentration play a lesser role in determining Fe/Cu ratios in Fe-precipitates. The method was evaluated by applying it in a fourth, naturally acidic stream unaffected by mining, where estimated pre-mining pH and Cu concentrations were similar to present-day values, and by demonstrating that inflows, particularly from unmined areas, had consistent effects on both the pre-mining and measured profiles of pH and Cu concentration. Using this method, it was estimated that mining has affected about 480 m of Daisy Creek, 1.8 km of Fisher Creek, and at least 1 km of Swift Gulch. Mean values of pH decreased by about 0.6 pH units to about 3.2 in Daisy Creek and by 1-1.5 pH units to about 3.5 in Fisher Creek. In Swift Gulch, mining appears to have decreased pH from about 5.5 to as low as 3.6. Dissolved Cu concentrations increased due to mining almost 40% in Daisy Creek to a mean of 11.7 mg/L and as much as 230% in Fisher Creek to 0.690 mg/L. Uncertainty in the fate of Cu during the conversion of Fe-precipitates to ferricrete translates to potential errors in pre-mining estimates of as much as 0.25 units

  16. Concentration and characterization of dissolved organic matter in the surface microlayer and subsurface water of the Bohai Sea, China

    NASA Astrophysics Data System (ADS)

    Chen, Yan; Yang, Gui-Peng; Wu, Guan-Wei; Gao, Xian-Chi; Xia, Qing-Yan

    2013-01-01

    A total of 19 sea-surface microlayer and corresponding subsurface samples collected from the Bohai Sea, China in April 2010 were analyzed for chlorophyll a, dissolved organic carbon (DOC) and its major compound classes including total dissolved carbohydrates (TDCHO, including monosaccharides, MCHO, and polysaccharides, PCHO) and total hydrolysable amino acids (THAA, including dissolved free, DFAA, and combined fraction, DCAA). The concentrations of DOC in the subsurface water ranged from 130.2 to 407.7 μM C, with an average of 225.9±75.4 μM C, while those in the surface microlayer varied between 140.1 and 330.9 μM C, with an average of 217.8±56.8 μM C. The concentrations of chlorophyll a, DOC, TDCHO and THAA in the microlayer were, respectively correlated with their subsurface water concentrations, implying that there was a strong exchange effect between the microlayer and subsurface water. The concentrations of DOC and TDCHO were negatively correlated with salinity, respectively, indicating that water mixing might play an important role in controlling the distribution of DOC and TDCHO in the water column. Major constituents of DCAA and DFAA present in the study area were glycine, alanine, glutamic acid, serine and histidine. Principal component analysis (PCA) was applied to examine the complex compositional differences that existed among the sampling sites. Our results showed that DFAA had higher mole percentages of glycine, valine and serine in the microlayer than in the subsurface water, while DCAA tended to have higher mole percentages of glutamic acid, aspartic acid, threonine, arginine, alanine, tyrosine, phenylalanine and leucine in the microlayer. The yields of TDCHO and THAA exhibited similar trends between the microlayer and subsurface water. Carbohydrate species displayed significant enrichment in the microlayer, whereas the DFAA and DCAA exhibited non-uniform enrichment in the microlayer.

  17. Variation of dissolved organic nitrogen concentration during the ultrasonic pretreatment to Microcystis aeruginosa.

    PubMed

    Liu, Cheng; Wang, Jie; Cao, Zhen; Chen, Wei; Bi, Hongkai

    2016-03-01

    Algae cells were the main sources of dissolved organic nitrogen (DON) in raw water with plenty of algae, and ultrasonic pretreatment was one of the algae-controlling methods through the damage of algae cells. However, the variation of DON concentration during the ultrasonic treatment process was not confirmed. Variation of DON concentration during the processes of low frequency ultrasound treatment of Microcystis aeruginosa was investigated. In addition, the effect of sonication on the metabolite concentration, algae cellar activity and the subsequent coagulation performance were discussed. The results showed that after a long duration of ultrasonic (60 s), nearly 90% of the algal cells were damaged and the maximum concentration of DON attained more than 3 mg/L. In order to control the leakage extent of DON, the sonication time should be less than 30 s with power intensity of more than 1.0 W/cm(3). In the mean time, ultrasonic treatment could inhibit the reactivation and the proliferation of algal, keep the algae cell wall integrity and enhance coagulation effectively under the same condition. However, ultrasound frequency had little effect on DON at the frequency range used in this study (20-150 kHz). Copyright © 2015 Elsevier B.V. All rights reserved.

  18. Shifts in Rumen Fermentation and Microbiota Are Associated with Dissolved Ruminal Hydrogen Concentrations in Lactating Dairy Cows Fed Different Types of Carbohydrates.

    PubMed

    Wang, Min; Wang, Rong; Xie, Tian Yu; Janssen, Peter H; Sun, Xue Zhao; Beauchemin, Karen A; Tan, Zhi Liang; Gao, Min

    2016-09-01

    Different carbohydrates ingested greatly influence rumen fermentation and microbiota and gaseous methane emissions. Dissolved hydrogen concentration is related to rumen fermentation and methane production. We tested the hypothesis that carbohydrates ingested greatly alter the rumen environment in dairy cows, and that dissolved hydrogen concentration is associated with these changes in rumen fermentation and microbiota. Twenty-eight lactating Chinese Holstein dairy cows [aged 4-5 y, body weight 480 ± 37 kg (mean ± SD)] were used in a randomized complete block design to investigate effects of 4 diets differing in forage content (45% compared with 35%) and source (rice straw compared with a mixture of rice straw and corn silage) on feed intake, rumen fermentation, and microbial populations. Feed intake (10.7-12.6 kg/d) and fiber degradation (0.584-0.692) greatly differed (P ≤ 0.05) between cows fed the 4 diets, leading to large differences (P ≤ 0.05) in gaseous methane yield (27.2-37.3 g/kg organic matter digested), dissolved hydrogen (0.258-1.64 μmol/L), rumen fermentation products, and microbiota. Ruminal dissolved hydrogen was negatively correlated (r < -0.40; P < 0.05) with molar proportion of acetate, numbers of fungi, abundance of Fibrobacter succinogenes, and methane yield, but positively correlated (r > 0.40; P < 0.05) with molar proportions of propionate and n-butyrate, numbers of methanogens, and abundance of Selenomonas ruminantium and Prevotella spp. Ruminal dissolved hydrogen was positively correlated (r = 0.93; P < 0.001) with Gibbs free energy changes of reactions producing greater acetate and hydrogen, but not correlated with those reactions producing more propionate without hydrogen. Changes in fermentation pathways from acetate toward propionate production and in microbiota from fibrolytic toward amylolytic species were closely associated with ruminal dissolved hydrogen in lactating dairy cows. An unresolved paradox was that greater dissolved

  19. Hydrologic control of dissolved organic matter concentration and quality in a semiarid artificially drained agricultural catchment

    NASA Astrophysics Data System (ADS)

    Bellmore, Rebecca A.; Harrison, John A.; Needoba, Joseph A.; Brooks, Erin S.; Kent Keller, C.

    2015-10-01

    Agricultural practices have altered watershed-scale dissolved organic matter (DOM) dynamics, including in-stream concentration, biodegradability, and total catchment export. However, mechanisms responsible for these changes are not clear, and field-scale processes are rarely directly linked to the magnitude and quality of DOM that is transported to surface water. In a small (12 ha) agricultural catchment in eastern Washington State, we tested the hypothesis that hydrologic connectivity in a catchment is the dominant control over the concentration and quality of DOM exported to surface water via artificial subsurface drainage. Concentrations of dissolved organic carbon (DOC) and humic-like components of DOM decreased while the Fluorescence Index and Freshness Index increased with depth through the soil profile. In drain discharge, these characteristics were significantly correlated with drain flow across seasons and years, with drain DOM resembling deep sources during low-flow and shallow sources during high flow, suggesting that DOM from shallow sources bypasses removal processes when hydrologic connectivity in the catchment is greatest. Assuming changes in streamflow projected for the Palouse River (which contains the study catchment) under the A1B climate scenario (rapid growth, dependence on fossil fuel, and renewable energy sources) apply to the study catchment, we project greater interannual variability in annual DOC export in the future, with significant increases in the driest years. This study highlights the variability in DOM inputs from agricultural soil to surface water on daily to interannual time scales, pointing to the need for a more nuanced understanding of agricultural impacts on DOM dynamics in surface water.

  20. Dissolved black carbon in the global cryosphere: Concentrations and chemical signatures

    NASA Astrophysics Data System (ADS)

    Khan, Alia L.; Wagner, Sasha; Jaffe, Rudolf; Xian, Peng; Williams, Mark; Armstrong, Richard; McKnight, Diane

    2017-06-01

    Black carbon (BC) is derived from the incomplete combustion of biomass and fossil fuels and can enhance glacial recession when deposited on snow and ice surfaces. Here we explore the influence of environmental conditions and the proximity to anthropogenic sources on the concentration and composition of dissolved black carbon (DBC), as measured by benzenepolycaroxylic acid (BPCA) markers, across snow, lakes, and streams from the global cryosphere. Data are presented from Antarctica, the Arctic, and high alpine regions of the Himalayas, Rockies, Andes, and Alps. DBC concentrations spanned from 0.62 μg/L to 170 μg/L. The median and (2.5, 97.5) quantiles in the pristine samples were 1.8 μg/L (0.62, 12), and nonpristine samples were 21 μg/L (1.6, 170). DBC is susceptible to photodegradation when exposed to solar radiation. This process leads to a less condensed BPCA signature. In general, DBC across the data set was composed of less polycondensed DBC. However, DBC from the Greenland Ice Sheet (GRIS) had a highly condensed BPCA molecular signature. This could be due to recent deposition of BC from Canadian wildfires. Variation in DBC appears to be driven by a combination of photochemical processing and the source combustion conditions under which the DBC was formed. Overall, DBC was found to persist across the global cryosphere in both pristine and nonpristine snow and surface waters. The high concentration of DBC measured in supraglacial melt on the GRIS suggests that DBC can be mobilized across ice surfaces. This is significant because these processes may jointly exacerbate surface albedo reduction in the cryosphere.Plain Language SummaryHere we present <span class="hlt">dissolved</span> black carbon (DBC) results for snow and glacial melt systems in Antarctica, the Arctic, and high alpine regions of the Himalayas, Rockies, Andes, and Alps. Across the global cryosphere, DBC composition appears to be a result of photochemical processes occurring</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li class="active"><span>6</span></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_6 --> <div id="page_7" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li class="active"><span>7</span></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="121"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/10099515','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/10099515"><span>Prediction of <span class="hlt">dissolved</span> oxygen and carbon dioxide <span class="hlt">concentration</span> profiles in tubular photobioreactors for microalgal culture</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rubio; Fernandez; Perez; Camacho; Grima</p> <p>1999-01-05</p> <p>A model is developed for prediction of axial <span class="hlt">concentration</span> profiles of <span class="hlt">dissolved</span> oxygen and carbon dioxide in tubular photobioreactors used for culturing microalgae. Experimental data are used to verify the model for continuous outdoor culture of Porphyridium cruentum grown in a 200-L reactor with 100-m long tubular solar receiver. The culture was carried out at a dilution rate of 0.05 h-1 applied only during a 10-h daylight period. The quasi-steady state biomass <span class="hlt">concentration</span> achieved was 3.0 g. L-1, corresponding to a biomass productivity of 1.5 g. L-1. d-1. The model could predict the <span class="hlt">dissolved</span> oxygen level in both gas disengagement zone of the reactor and at the end of the loop, the exhaust gas composition, the amount of carbon dioxide injected, and the pH of the culture at each hour. In predicting the various parameters, the model took into account the length of the solar receiver tube, the rate of photosynthesis, the velocity of flow, the degree of mixing, and gas-liquid mass transfer. Because the model simulated the system behavior as a function of tube length and operational variables (superficial gas velocity in the riser, composition of carbon dioxide in the gas injected in the solar receiver and its injection rate), it could potentially be applied to rational design and scale-up of photobioreactors. Copyright 1999 John Wiley & Sons, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010AGUFM.B13D0516V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010AGUFM.B13D0516V"><span>Temporal Variability of Stemflow <span class="hlt">Dissolved</span> Organic Carbon (DOC) <span class="hlt">Concentrations</span> and Quality from Morphologically Contrasting Deciduous Canopies</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>van Stan, J. T.; Levia, D. F.; Inamdar, S. P.; Mitchell, M. J.; Mage, S. M.</p> <p>2010-12-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) inputs from canopy-derived hydrologic fluxes play a significant role in the terrestrial carbon budgets of forested ecosystems. However, no studies known to the authors have examined the variability of both DOC <span class="hlt">concentrations</span> and quality for stemflow across time scales, nor has any study to date evaluated the effects of canopy structure on stemflow DOC characteristics. This investigation seeks to rectify this knowledge gap by examining the variability of stemflow DOC <span class="hlt">concentrations</span> and quality across contrasting canopy morphologies and time scales (seasonal, storm and intrastorm). Bulk and intrastorm stemflow samples from a less dense, rough-barked, more plagiophile (Liriodendron tulipifera L. (tulip poplar)) and a denser, thin-barked, more erectophile (Fagus grandifolia Ehrh. (American beech)) canopy were collected and analyzed for DOC quality using metrics derived from UV-vis spectroscopy (E2:E3 ratio, SUVA254, select spectral slope (S), and spectral slope ratios (SR)). Our results suggest that stemflow DOC <span class="hlt">concentrations</span> and quality change as crown architectural traits enhance or diminish hydrologic retention time within the canopy. The architecture of L. tulipifera canopies likely retards the flow of intercepted water, increasing chemical exchange with bark and foliar surfaces. UV-vis metrics indicated that this increased chemical exchange, particularly with bark surfaces, generally enhanced aromatic hydrocarbon content and increased molecular weight. Because leaf presence influenced DOC quality, stemflow DOC characteristics also varied seasonally in response to canopy condition. At the inter- and intrastorm scale, stemflow DOC <span class="hlt">concentration</span> and quality varied with meteorological and antecedent canopy conditions. Since recent studies have linked stemflow production to preferential subsurface transport of <span class="hlt">dissolved</span> chemistries, trends in DOC speciation and fluxes described in this study may impact soil environments within wooded</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2018/5001/sir20185001.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2018/5001/sir20185001.pdf"><span>Assessment of <span class="hlt">dissolved</span>-selenium <span class="hlt">concentrations</span> and loads in the lower Gunnison River Basin, Colorado, as part of the Selenium Management Program, from 2011 to 2016</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Henneberg, Mark F.</p> <p>2018-04-23</p> <p>The Gunnison Basin Selenium Management Program implemented a water-quality monitoring network in 2011 in the lower Gunnison River Basin in Colorado. Selenium is a trace element that bioaccumulates in aquatic food chains and can cause reproductive failure, deformities, and other harmful effects. This report presents the percentile values of selenium because regulatory agencies in Colorado make decisions based on the U.S. Environmental Protection Agency (EPA) Clean Water Act Section 303(d) that uses percentile values of <span class="hlt">concentration</span>. Also presented are <span class="hlt">dissolved</span>-selenium loads at 18 sites in the lower Gunnison River Basin for water years (WYs) 2011–2016 (October 1, 2010, through September 30, 2016). Annual <span class="hlt">dissolved</span>-selenium loads were calculated for five sites with continuous U.S. Geological Survey (USGS) streamflow-gaging stations. Annual <span class="hlt">dissolved</span>-selenium loads for WY 2011 through WY 2016 ranged from 179 and 391 pounds (lb) at Uncompahgre River at Colona to 11,100 and 17,300 lb at Gunnison River near Grand Junction (herein called Whitewater), respectively. Instantaneous loads were calculated for five sites with continuous U.S. Geological Survey (USGS) streamflow-gaging stations and 13 ancillary sites where discrete water-quality sampling also took place, using discrete water-quality samples and the associated discharge measurements collected during the period. Median instantaneous loads ranged from 0.01 pound per day (lb/d) at Smith Fork near Lazear to 33.0 lb/d at Whitewater. Mean instantaneous loads ranged from 0.06 lb/d at Smith Fork near Lazear to 36.2 lb/d at Whitewater. Most tributary sites in the basin had a median instantaneous <span class="hlt">dissolved</span>-selenium load of less than 20.0 lb/day. In general, <span class="hlt">dissolved</span>-selenium loads at Gunnison River main-stem sites showed an increase from upstream to downstream. The State of Colorado water-quality standard for <span class="hlt">dissolved</span> selenium of 4.6 micrograms per liter (µg/L) was compared to the 85th percentiles for <span class="hlt">dissolved</span></p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25277967','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25277967"><span>Characterization and biotoxicity assessment of <span class="hlt">dissolved</span> organic matter in RO <span class="hlt">concentrate</span> from a municipal wastewater reclamation reverse osmosis system.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Sun, Ying-Xue; Gao, Yue; Hu, Hong-Ying; Tang, Fang; Yang, Zhe</p> <p>2014-12-01</p> <p>Reverse osmosis (RO) <span class="hlt">concentrate</span> from municipal wastewater reclamation reverse osmosis (mWRRO) system containing organic compounds may associate with toxic risk, and its discharge might pose an environmental risk. To identify a basis for the selection of feasible technology in treating RO <span class="hlt">concentrates</span>, the characteristics and biotoxicity of different fractions of <span class="hlt">dissolved</span> organic matter (DOM) in RO <span class="hlt">concentrates</span> from an mWRRO system were investigated. The results indicated that the hydrophilic neutrals (HIN), hydrophobic acids (HOA) and hydrophobic bases (HOB) accounted for 96% of the <span class="hlt">dissolved</span> organic carbon (DOC) of the total DOM in the RO <span class="hlt">concentrate</span>. According to the SEC chromatograph detected at 254 nm wavelength of UV, the DOM with molecular weight (MW) 1-3 kDa accounted for the majority of the basic and neutral fractions. The fluorescence spectra of the excitation emission matrix (EEM) indicated that most aromatic proteins, humic/fulvic acid-like and soluble microbial by-product-like substances existed in the fractions HOA and hydrophobic neutrals (HON). The genotoxicity and anti-estrogenic activity of the RO <span class="hlt">concentrate</span> were 1795.6 ± 57.2 μg 4-NQOL(-1) and 2.19 ± 0.05 mg TAM L(-1), respectively. The HIN, HOA, and HOB contributed to the genotoxicity of the RO <span class="hlt">concentrate</span>, and the HIN was with the highest genotoxic level of 1007.9 ± 94.8 μg 4-NQOL(-1). The HOA, HON, and HIN lead to the total anti-estrogenic activity of the RO <span class="hlt">concentrate</span>, and HOA occupied approximately 60% of the total, which was 1.3 ± 0.17 mg TAM L(-1). Copyright © 2014 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2012/5049/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2012/5049/"><span>Methods for evaluating temporal groundwater quality data and results of decadal-scale changes in chloride, <span class="hlt">dissolved</span> solids, and nitrate <span class="hlt">concentrations</span> in groundwater in the United States, 1988-2010</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Lindsey, Bruce D.; Rupert, Michael G.</p> <p>2012-01-01</p> <p>Decadal-scale changes in groundwater quality were evaluated by the U.S. Geological Survey National Water-Quality Assessment (NAWQA) Program. Samples of groundwater collected from wells during 1988-2000 - a first sampling event representing the decade ending the 20th century - were compared on a pair-wise basis to samples from the same wells collected during 2001-2010 - a second sampling event representing the decade beginning the 21st century. The data set consists of samples from 1,236 wells in 56 well networks, representing major aquifers and urban and agricultural land-use areas, with analytical results for chloride, <span class="hlt">dissolved</span> solids, and nitrate. Statistical analysis was done on a network basis rather than by individual wells. Although spanning slightly more or less than a 10-year period, the two-sample comparison between the first and second sampling events is referred to as an analysis of decadal-scale change based on a step-trend analysis. The 22 principal aquifers represented by these 56 networks account for nearly 80 percent of the estimated withdrawals of groundwater used for drinking-water supply in the Nation. Well networks where decadal-scale changes in <span class="hlt">concentrations</span> were statistically significant were identified using the Wilcoxon-Pratt signed-rank test. For the statistical analysis of chloride, <span class="hlt">dissolved</span> solids, and nitrate <span class="hlt">concentrations</span> at the network level, more than half revealed no statistically significant change over the decadal period. However, for networks that had statistically significant changes, increased <span class="hlt">concentrations</span> outnumbered decreased <span class="hlt">concentrations</span> by a large margin. Statistically significant increases of chloride <span class="hlt">concentrations</span> were identified for 43 percent of 56 networks. <span class="hlt">Dissolved</span> solids <span class="hlt">concentrations</span> increased significantly in 41 percent of the 54 networks with <span class="hlt">dissolved</span> solids data, and nitrate <span class="hlt">concentrations</span> increased significantly in 23 percent of 56 networks. At least one of the three - chloride, <span class="hlt">dissolved</span> solids, or</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013BGeo...10..917M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013BGeo...10..917M"><span>Estimating absorption coefficients of colored <span class="hlt">dissolved</span> organic matter (CDOM) using a semi-analytical algorithm for southern Beaufort Sea waters: application to deriving <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon from space</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Matsuoka, A.; Hooker, S. B.; Bricaud, A.; Gentili, B.; Babin, M.</p> <p>2013-02-01</p> <p>A series of papers have suggested that freshwater discharge, including a large amount of <span class="hlt">dissolved</span> organic matter (DOM), has increased since the middle of the 20th century. In this study, a semi-analytical algorithm for estimating light absorption coefficients of the colored fraction of DOM (CDOM) was developed for southern Beaufort Sea waters using remote sensing reflectance at six wavelengths in the visible spectral domain corresponding to MODIS ocean color sensor. This algorithm allows the separation of colored detrital matter (CDM) into CDOM and non-algal particles (NAP) through the determination of NAP absorption using an empirical relationship between NAP absorption and particle backscattering coefficients. Evaluation using independent datasets, which were not used for developing the algorithm, showed that CDOM absorption can be estimated accurately to within an uncertainty of 35% and 50% for oceanic and coastal waters, respectively. A previous paper (Matsuoka et al., 2012) showed that <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentrations</span> were tightly correlated with CDOM absorption in our study area (r2 = 0.97). By combining the CDOM absorption algorithm together with the DOC versus CDOM relationship, it is now possible to estimate DOC <span class="hlt">concentrations</span> in the near-surface layer of the southern Beaufort Sea using satellite ocean color data. DOC <span class="hlt">concentrations</span> in the surface waters were estimated using MODIS ocean color data, and the estimates showed reasonable values compared to in situ measurements. We propose a routine and near real-time method for deriving DOC <span class="hlt">concentrations</span> from space, which may open the way to an estimate of DOC budgets for Arctic coastal waters.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70177908','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70177908"><span>Effect of phytoremediation on <span class="hlt">concentrations</span> of benzene, toluene, naphthalene, and <span class="hlt">dissolved</span> oxygen in groundwater at a former manufactured gas plant site, Charleston, South Carolina, USA, 1998–2014</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Landmeyer, James E.; Effinger, Thomas N.</p> <p>2016-01-01</p> <p><span class="hlt">Concentrations</span> of benzene, toluene, naphthalene, and <span class="hlt">dissolved</span> oxygen in groundwater at a former manufactured gas plant site near Charleston, South Carolina, USA, have been monitored since the installation of a phytoremediation system of hybrid poplar trees in 1998. Between 2000 and 2014, the <span class="hlt">concentrations</span> of benzene, toluene, and naphthalene (BT&N) in groundwater in the planted area have decreased. For example, in the monitoring well containing the highest <span class="hlt">concentrations</span> of BT&N, benzene <span class="hlt">concentrations</span> decreased from 10,200 µg/L to less than 4000 µg/L, toluene <span class="hlt">concentrations</span> decreased from 2420 µg/L to less than 20 µg/L, and naphthalene <span class="hlt">concentrations</span> decreased from 6840 µg/L to less than 3000 µg/L. <span class="hlt">Concentrations</span> of BT&N in groundwater in all wells were observed to be lower during the summer months relative to the winter months of a particular year during the first few years after installing the phytoremediation system, most likely due to increased transpiration and contaminant uptake by the hybrid poplar trees during the warm summer months; this pathway of uptake by trees was confirmed by the detection of benzene, toluene, and naphthalene in trees during sampling events in 2002, and later in the study in 2012. These data suggest that the phytoremediation system affects the groundwater contaminants on a seasonal basis and, over multiple years, has resulted in a cumulative decrease in <span class="hlt">dissolved</span>-phase contaminant <span class="hlt">concentrations</span> in groundwater. The removal of <span class="hlt">dissolved</span> organic contaminants from the aquifer has resulted in a lower demand on <span class="hlt">dissolved</span> oxygen supplied by recharge and, as a result, the redox status of the groundwater has changed from anoxic to oxic conditions. This study provides much needed information for water managers and other scientists on the viability of the long-term effectiveness of phytoremediation in decreasing groundwater contaminants and increasing <span class="hlt">dissolved</span> oxygen at sites contaminated by benzene, toluene, and naphthalene.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/15900439','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/15900439"><span>Feedforward-feedback control of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in a predenitrification system.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yong, Ma; Yongzhen, Peng; Shuying, Wang</p> <p>2005-07-01</p> <p>As the largest single energy-consuming component in most biological wastewater treatment systems, aeration control is of great interest from the point of view of saving energy and improving wastewater treatment plant efficiency. In this paper, three different strategies, including conventional constant <span class="hlt">dissolved</span> oxygen (DO) set-point control, cascade DO set-point control, and feedforward-feedback DO set-point control were evaluated using the denitrification layout of the IWA simulation benchmark. Simulation studies showed that the feedforward-feedback DO set-point control strategy was better than the other control strategies at meeting the effluent standards and reducing operational costs. The control strategy works primarily by feedforward control based on an ammonium sensor located at the head of the aerobic process. It has an important advantage over effluent measurements in that there is no (or only a very short) time delay for information; feedforward control was combined with slow feedback control to compensate for model approximations. The feedforward-feedback DO control was implemented in a lab-scale wastewater treatment plant for a period of 60 days. Compared to operation with constant DO <span class="hlt">concentration</span>, the required airflow could be reduced by up to 8-15% by employing the feedforward-feedback DO-control strategy, and the effluent ammonia <span class="hlt">concentration</span> could be reduced by up to 15-25%. This control strategy can be expected to be accepted by the operating personnel in wastewater treatment plants.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004AGUSM.H21D..03S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004AGUSM.H21D..03S"><span>Diminished Stream Nitrate <span class="hlt">Concentrations</span> Linked to <span class="hlt">Dissolved</span> Organic Carbon Dynamics After Leaf Fall</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sebestyen, S. D.; Shanley, J. B.; Boyer, E. W.; Doctor, D. H.; Kendall, C.</p> <p>2004-05-01</p> <p>Thermodynamic coupling of the nitrogen and carbon cycles has broad implications for controls on catchment nutrient fluxes. In the northeast US, leaf fall occurs in early October and the availability of organic carbon increases as the leaves decompose. At the Sleepers River Research Watershed in northeastern Vermont (USA), we sampled stream chemistry from seven nested catchments to determine how stream <span class="hlt">dissolved</span> organic carbon (DOC) and nitrate vary as a function of flow conditions, land-use, and basin size in response to leaf fall. Following leaf fall, nitrate <span class="hlt">concentration</span> patterns were quantitatively different from other times of the year. Under baseflow conditions, stream and soil water DOC <span class="hlt">concentrations</span> were higher than normal, whereas nitrate <span class="hlt">concentrations</span> declined sharply at the five smallest catchments and more modestly at the two largest catchments. Under high flow conditions, flushing of nitrate was observed, as is typical for stormflow response at Sleepers River. Our field data suggest that in-stream processing of nitrate is likely thermodynamically and kinetically favorable under baseflow but not at higher flow conditions when expanding variable source areas make hydrological connections between nitrate source areas and streams. We are working to evaluate this hypothesis with isotopic and other monitoring data, and to model the coupled interactions of water, DOC, and nitrate fluxes in these nested catchments.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2008/5001/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2008/5001/"><span><span class="hlt">Dissolved</span>-solids transport in surface water of the Muddy Creek Basin, Utah</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Gerner, Steven J.</p> <p>2008-01-01</p> <p>Muddy Creek is located in the southeastern part of central Utah and is a tributary of the Dirty Devil River, which, in turn, is a tributary of the Colorado River. <span class="hlt">Dissolved</span> solids transported from the Muddy Creek Basin may be stored in the lower Dirty Devil River Basin, but are eventually discharged to the Colorado River and impact downstream water users. This study used selected <span class="hlt">dissolved</span>-solids measurements made by various local, State, and Federal agencies from the 1970s through 2006, and additional <span class="hlt">dissolved</span>-solids data that were collected by the U.S. Geological Survey during April 2004 through November 2006, to compute <span class="hlt">dissolved</span>-solids loads, determine the distribution of <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>, and identify trends in <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> in surface water of the Muddy Creek Basin. The <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> values measured in water samples collected from Muddy Creek during April 2004 through October 2006 ranged from 385 milligrams per liter (mg/L) to 5,950 mg/L. The highest <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> values measured in the study area were in water samples collected at sites in South Salt Wash (27,000 mg/L) and Salt Wash (4,940 to 6,780 mg/L). The mean annual <span class="hlt">dissolved</span>-solids load in Muddy Creek for the periods October 1976 to September 1980 and October 2005 to September 2006 was smallest at a site near the headwaters (9,670 tons per year [tons/yr]) and largest at a site at the mouth (68,700 tons/yr). For this period, the mean annual yield of <span class="hlt">dissolved</span> solids from the Muddy Creek Basin was 44 tons per square mile. During October 2005 to September 2006, direct runoff transported as much as 45 percent of the annual <span class="hlt">dissolved</span>-solids load at the mouth of Muddy Creek. A storm that occurred during October 5?7, 2006 resulted in a peak streamflow at the mouth of Muddy Creek of 7,150 cubic feet per second (ft3/s) and the transport of an estimated 35,000 tons of <span class="hlt">dissolved</span> solids, which is about 51 percent of the average annual <span class="hlt">dissolved</span></p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=331162&Lab=NHEERL&keyword=organic+AND+chemistry&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=331162&Lab=NHEERL&keyword=organic+AND+chemistry&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Evaluating the precision of passive sampling methods using PRCs in the water column</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Low-Density polyethylene (LDPE) sheets are often used as passive samplers for aquatic environmental monitoring to measure the <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> of hydrophobic organic contaminants (HOCs). HOCs that are <span class="hlt">freely</span> <span class="hlt">dissolved</span> in water (Cfree) will partition into the LDPE until a ...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C13B0956K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C13B0956K"><span><span class="hlt">Dissolved</span> black carbon in the global cryosphere: <span class="hlt">concentrations</span> and chemical signatures</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Khan, A. L.; Wagner, S.; Jaffe, R.; Xian, P.; Williams, M. W.; Armstrong, R. L.; McKnight, D. M.</p> <p>2017-12-01</p> <p>Black carbon (BC) is derived from the incomplete combustion of biomass and fossil fuels and can enhance glacial recession when deposited on snow and ice surfaces. Here we explore the influence of environmental conditions and the proximity to anthropogenic sources on the <span class="hlt">concentration</span> and composition of <span class="hlt">dissolved</span> black carbon (DBC), as measured by benzenepolycaroxylic acid (BPCA) markers, across snow, lakes, and streams from the global cryosphere. Data are presented from Antarctica, the Arctic, and high alpine regions of the Himalayas, Rockies, Andes, and Alps. DBC <span class="hlt">concentrations</span> spanned from 0.62 μg/L to 170 μg/L. The median and (2.5, 97.5) quantiles in the pristine samples were 1.8 μg/L (0.62, 12), and non-pristine samples were 21 μg/L (1.6, 170). DBC is susceptible to photodegradation when exposed to solar radiation. This process leads to a less condensed BPCA signature. In general, DBC across the dataset was comprised of less-polycondensed DBC. However, DBC from the Greenland Ice Sheet (GRIS) had a highly-condensed BPCA molecular signature. This could be due to recent deposition of BC from Canadian wildfires. Variation in DBC appears to be driven by a combination of photochemical processing and the source combustion conditions under which the DBC was formed. Overall, DBC was found to persist across the global cryosphere in both pristine and non-pristine snow and surface waters. The high <span class="hlt">concentration</span> of DBC measured in supra-glacial melt on the GRIS suggests DBC can be mobilized across ice surfaces. This is significant because these processes may jointly exacerbate surface albedo reduction in the cryosphere.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70180384','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70180384"><span>Mercury dynamics in relation to <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentration</span> and quality during high flow events in three northeastern U.S. streams</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Dittman, Jason A.; Shanley, James B.; Driscoll, Charles T.; Aiken, George R.; Chalmers, Ann T.; Towse, Janet E.; Selvendiran, Pranesh</p> <p>2010-01-01</p> <p>Mercury (Hg) contamination is widespread in remote areas of the northeastern United States. Forested uplands have accumulated a large reservoir of Hg in soil from decades of elevated anthropogenic deposition that can be released episodically to stream water during high flows. The objective of this study was to evaluate spatial and temporal variations in stream water Hg species and organic matter fractions over a range of hydrologic conditions in three forested upland watersheds (United States). Mercury and organic matter <span class="hlt">concentrations</span> increased with discharge at all three sites; however, the partitioning of Hg fractions (<span class="hlt">dissolved</span> versus particulate) differed among sites and seasons. Associated with increased discharge, flow paths shifted from mineral soil under base flow to upper soil horizons. As flow paths shifted, greater <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon (DOC) richer in aromatic substances were flushed from upper soil horizons to stream water. The hydrophobic organic matter associated with humic material from upper soils appears to have had a greater capacity to bind Hg. Because of the strong correlation between Hg and DOC, we hypothesize that there was a concurrent shift in the source of Hg with DOC from lower mineral soil to upper soil horizons. Our study suggests that stream discharge is an effective predictor of <span class="hlt">dissolved</span> total Hg flux.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23040354','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23040354"><span>Image analyzing method to evaluate in situ bioluminescence from an obligate anaerobe cultivated under various <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ninomiya, Kazuaki; Yamada, Ryuji; Matsumoto, Masami; Fukiya, Satoru; Katayama, Takane; Ogino, Chiaki; Shimizu, Nobuaki</p> <p>2013-02-01</p> <p>An image analyzing method was developed to evaluate in situ bioluminescence expression, without exposing the culture sample to the ambient oxygen atmosphere. Using this method, we investigated the effect of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on bioluminescence from an obligate anaerobe Bifidobacterium longum expressing bacterial luciferase which catalyzes an oxygen-requiring bioluminescent reaction. Copyright © 2012 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28463824','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28463824"><span>Impact of the excess sludge modification with selected chemical reagents on the increase of <span class="hlt">dissolved</span> organic substances <span class="hlt">concentration</span> compounds transformations in activated sludge.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zawieja, Iwona; Lidia, Wolny; Marta, Próba</p> <p>2017-07-01</p> <p>Submission of excess sludge initial disintegration process significantly affects the efficiency of anaerobic stabilization process. Expression of increasing the <span class="hlt">concentration</span> of organic matter in <span class="hlt">dissolved</span> form is to increase sludge disintegration. As a result of chemical modification is an increase of the chemical oxygen demand and the <span class="hlt">concentration</span> of volatile fatty acids. The aim of this study was to determine the impact of the disintegration process with selected chemical reagents to increase the <span class="hlt">concentration</span> of organic substances in <span class="hlt">dissolved</span> form. The process of chemical disintegration of excess sludge was treated using the following reagents: Mg(OH) 2 , Ca(OH) 2 , HCl, H 2 SO 4 , H 2 O 2 . The modification was carried out at ambient temperature for 2, 6 and 24h. During sludge disintegration it was noticed the growth of indicators values that confirmed the susceptibility of prepared sludge to biodegradation. Copyright © 2017 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015EGUGA..17.5270L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015EGUGA..17.5270L"><span>Long term in situ monitoring of total <span class="hlt">dissolved</span> iron <span class="hlt">concentrations</span> on the MoMAR observatory</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Laes-Huon, Agathe; Legrand, Julien; Tanguy, Virginie; Cathalot, Cecile; Blandin, Jérôme; Rolin, Jean-Francois; Sarradin, Pierre-Marie</p> <p>2015-04-01</p> <p>Nowadays the scientific community wants relevant monitoring with an increase in spatial and temporal distribution of key chemicals. The hydrothermal ecosystems characterized by strong physico-chemical gradients are also of particular interest as they present an unique fauna, sustained by microbial chemosynthesis. The characterization of the chemical environment in the hydrothermal vent ecosystems implies the use of in situ instrumentation which is a serious challenge in the marine environment (Prien et al. 2007). The CHEMINI (CHEmical MINIaturised analyser), presented here, is a chemical in situ analyser specialized for deep sea uses (Vuillemin et al. 2007). It was first deployed on the autonomous deep sea observatory MoMAR (Monitoring of the Mid-Atlantic Ridge, FIXO3, Fixed point Open Ocean Observatories) in 2010. The first part of the presentation will focus on the description of the CHEMINI, then on the results obtained on the MoMAR observatory during the last 4 years. CHEMINI, implemented on the TEMPO ecological module determined total <span class="hlt">dissolved</span> iron <span class="hlt">concentrations</span> associated with an optode and a temperature probe. Several months of total iron <span class="hlt">concentrations</span>, of T°C and videos were recorded permitting the study of the temporal dynamics of faunal assemblages and their habitat on the Lucky strike vent (-1700m, Cuvelier et al. 2011). Long term in situ analysis of total <span class="hlt">dissolved</span> iron (31st of August 2013 - 23rd of February 2014, [DFe] = 7.12 +- 2.11 µmol L-1, n = 519) at the Eiffel Tower edifice is presented in details. The daily analyzed in situ standard (25µmol.L-1) showed an excellent reproducibility (1.07%, n=522). CHEMINI was reliable, robust over time for in situ analysis. The averaged total <span class="hlt">dissolved</span> iron <span class="hlt">concentrations</span> for the 6 months period remain low but they correlated significantly with temperature showing a spectra frequency with a maximal contribution around 4-5 days for both variables. The analytical results will be commented and the future</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012BGD.....913743M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012BGD.....913743M"><span>Estimating absorption coefficients of colored <span class="hlt">dissolved</span> organic matter (CDOM) using a semi-analytical algorithm for Southern Beaufort Sea (Canadian Arctic) waters: application to deriving <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon from space</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Matsuoka, A.; Hooker, S. B.; Bricaud, A.; Gentili, B.; Babin, M.</p> <p>2012-10-01</p> <p>A series of papers have suggested that freshwater discharge, including a large amount of <span class="hlt">dissolved</span> organic matter (DOM), has increased since the middle of the 20th century. In this study, a semi-analytical algorithm for estimating light absorption coefficients of the colored fraction of DOM (CDOM) was developed for Southern Beaufort Sea waters using remote sensing reflectance at six wavelengths in the visible spectral domain corresponding to MODIS ocean color sensor. This algorithm allows to separate colored detrital matter (CDM) into CDOM and non-algal particles (NAP) by determining NAP absorption using an empirical relationship between NAP absorption and particle backscattering coefficients. Evaluation using independent datasets, that were not used for developing the algorithm, showed that CDOM absorption can be estimated accurately to within an uncertainty of 35% and 50% for oceanic and turbid waters, respectively. In situ measurements showed that <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentrations</span> were tightly correlated with CDOM absorption (r2 = 0.97). By combining the CDOM absorption algorithm together with the DOC versus CDOM relationship, it is now possible to estimate DOC <span class="hlt">concentrations</span> in the near-surface layer of the Southern Beaufort Sea using satellite ocean color data. DOC <span class="hlt">concentrations</span> in the surface waters were estimated using MODIS ocean color data, and the estimates showed reasonable values compared to in situ measurements. We propose a routine and near real-time method for deriving DOC <span class="hlt">concentrations</span> from space, which may open the way to an estimate of DOC budgets for Arctic coastal waters.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29908734','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29908734"><span>Mercury photoreduction and photooxidation in lakes: Effects of filtration and <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentration</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>O'Driscoll, Nelson J; Vost, Emma; Mann, Erin; Klapstein, Sara; Tordon, Robert; Lukeman, Matthew</p> <p>2018-06-01</p> <p>Mercury is a globally distributed, environmental contaminant. Quantifying the retention and loss of mercury is integral for predicting mercury-sensitive ecosystems. There is little information on how <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentrations</span> and particulates affect mercury photoreaction kinetics in freshwater lakes. To address this knowledge gap, samples were collected from ten lakes in Kejimkujik National Park, Nova Scotia (DOC: 2.6-15.4mg/L). Filtered (0.2μm) and unfiltered samples were analysed for gross photoreduction, gross photooxidation, and net reduction rates of mercury using pseudo first-order curves. Unfiltered samples had higher <span class="hlt">concentrations</span> (p=0.04) of photoreducible divalent mercury (Hg(II) RED ) (mean of 754±253pg/L) than filtered samples (mean of 482±206pg/L); however, gross photoreduction and photooxidation rate constants were not significantly different in filtered or unfiltered samples in early summer. DOC was not significantly related to gross photoreduction rate constants in filtered (R 2 =0.43; p=0.08) and unfiltered (R 2 =0.02; p=0.71) samples; DOC was also not significantly related to gross photooxidation rate constants in filtered or unfiltered samples. However, DOC was significantly negatively related with Hg(II) RED in unfiltered (R 2 =0.53; p=0.04), but not in filtered samples (R 2 =0.04; p=0.60). These trends indicate that DOC is a factor in determining <span class="hlt">dissolved</span> mercury photoreduction rates and particles partially control available Hg(II) RED in lake water. This research also demonstrates that within these lakes gross photoreduction and photooxidation processes are close to being in balance. Changes to catchment inputs of particulate matter and DOC may alter mercury retention in these lakes and could partially explain observed increases of mercury accumulation in biota. Copyright © 2017. Published by Elsevier B.V.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22673628','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22673628"><span>Regulation of the <span class="hlt">dissolved</span> phosphate <span class="hlt">concentration</span> of a mountainous stream, Kitakyushu, southwestern Japan.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Koga, Masaaki; Yoshimura, Kazuhisa</p> <p>2012-07-01</p> <p>The phosphate <span class="hlt">concentration</span> in mountainous stream water can be a measure of the forest condition, because its <span class="hlt">concentration</span> will be low when the biomass in the forest is increasing and vice versa when the forest is declining. To investigate the seasonal change in the <span class="hlt">dissolved</span> phosphate <span class="hlt">concentration</span> of the mountainous stream water of the Yamakami River, Kitakyushu, from June 2009 to August 2010, and the regulation mechanism of the phosphate <span class="hlt">concentration</span>, solid-phase spectrophotometry, which can be applicable to natural water without any pretreatment procedures, was employed for the determination of phosphate at μg P L(-1) levels in natural water. The phosphate <span class="hlt">concentrations</span> in the mountainous stream waters at 6 sites ranged from 2.2 to 13 μg P L(-1), and those from the catchment area of the steady state forest were 5.3 ± 1.6 (±1 SD) μg P L(-1). Changes in the <span class="hlt">concentration</span> were fairly small even during a storm runoff. The average phosphate <span class="hlt">concentration</span> of rain was 2.8 ± 0.7 μg P L(-1), about half of the <span class="hlt">concentration</span> in the stream water. The rate of runoff in forest areas is generally considered to be about 50% of the total precipitation. For a forest under a climax condition, the phosphate <span class="hlt">concentration</span> is estimated to be regulated by the fallout and evapotranspiration (α = 0.05). At one of the sites, an upstream tributary, where a fairly big landslide occurred before July in 2009, the phosphate <span class="hlt">concentration</span> was the highest, suggesting that the biomass may still be decreasing. For all of the six sites examined, a characteristic seasonal change in phosphate <span class="hlt">concentration</span> was observed, reflecting the local budget between the biological decomposition of plant matter and the consumption by the biomass. The increase in the phosphate <span class="hlt">concentration</span> during late spring and early summer may result from the extensive decomposition of plant litter mainly supplied in autumn and of plant matter relating to spring blooming such as fallen flowers, pollen and immature</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JHyd..556..775W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JHyd..556..775W"><span>Declines in the <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentration</span> and flux from the UK</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Worrall, Fred; Howden, Nicholas J. K.; Burt, Tim P.; Bartlett, Rebecca</p> <p>2018-01-01</p> <p>Increased <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon (DOC) have been reported for many catchments across the northern hemisphere. Hypotheses to explain the increase have varied (eg. increasing air temperature or recovery from acidification) but one test of alternative hypotheses is the trend over the recent decade, with the competing hypotheses predicting: continuing increase; the rate of increase declining with time; and even decrease in <span class="hlt">concentration</span>. In this study, records of DOC <span class="hlt">concentration</span> in non-tidal rivers across the UK were examined for the period 2003-2012. The study found that: Of the 62 decade-long <span class="hlt">concentration</span> trends that could be examined, 3 showed a significant increase, 17 experienced no significant change and 42 showed a significant decrease; in 28 of the 42 significant decreases, a significant step change was apparent with step changes being a decrease in <span class="hlt">concentration</span> in every case. Of the 118 sites where annual flux and <span class="hlt">concentration</span> records were available from 1974, 28 showed a significant step change down in flux and 52 showed a step down in <span class="hlt">concentration</span>. The modal year of the step changes was 2000 with no step changes observed before 1982. At the UK national scale, DOC flux peaked in 2005 at 1354 ktonnes C/yr (5.55 tonnes C/km2/yr) but has declined since. The study suggests that there is a disconnection between DOC records from large catchments at their tidal limits and complementary records from headwater catchments, which means that mechanisms believed to be driving increases in DOC <span class="hlt">concentrations</span> in headwaters will not necessarily be those controlling trends in DOC <span class="hlt">concentration</span> further downstream. We propose that the changes identified here have been driven by changes in in-stream processing and changes brought about by the Urban Waste Water Treatment Directive. Therefore, signals identified in headwater catchments may bear little relation to those observed in large rivers much further downstream and vice versa.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li class="active"><span>7</span></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_7 --> <div id="page_8" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li class="active"><span>8</span></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="141"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=296409&Lab=NERL&keyword=marine+AND+pollution&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=296409&Lab=NERL&keyword=marine+AND+pollution&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span><span class="hlt">Dissolved</span> methane <span class="hlt">concentration</span> and flux in the coastal zone of the Southern California Bight-Mexican sector: Possible influence of wastewater</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>We measured <span class="hlt">dissolved</span> methane <span class="hlt">concentrations</span> ([CH4]) in the coastal zone of the Southern California Bight-Mexican sector (SCBMex) during two cruises: S1 in the USA–Mexico Border Area (BA) during a short rainstorm and S2 in the entire SCBMex during a drier period a few days later....</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18075103','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18075103"><span>Effect of TCE <span class="hlt">concentration</span> and <span class="hlt">dissolved</span> groundwater solutes on NZVI-promoted TCE dechlorination and H2 evolution.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Yueqiang; Phenrat, Tanapon; Lowry, Gregory V</p> <p>2007-11-15</p> <p>Nanoscale zero-valent iron (NZVI) is used to remediate contaminated groundwater plumes and contaminant source zones. The target contaminant <span class="hlt">concentration</span> and groundwater solutes (NO3-, Cl-, HCO3-, SO4(2-), and HPO4(2-)) should affect the NZVI longevity and reactivity with target contaminants, but these effects are not well understood. This study evaluates the effect of trichloroethylene (TCE) <span class="hlt">concentration</span> and common <span class="hlt">dissolved</span> groundwater solutes on the rates of NZVI-promoted TCE dechlorination and H2 evolution in batch reactors. Both model systems and real groundwater are evaluated. The TCE reaction rate constant was unaffected by TCE <span class="hlt">concentration</span> for [TCE] < or = 0.46 mM and decreased by less than a factor of 2 for further increases in TCE <span class="hlt">concentration</span> up to water saturation (8.4 mM). For [TCE] > or = 0.46 mM, acetylene formation increased, and the total amount of H2 evolved at the end of the particle reactive lifetime decreased with increasing [TCE], indicating a higher Fe0 utilization efficiency for TCE dechlorination. Common groundwater anions (5mN) had a minor effect on H2 evolution but inhibited TCE reduction up to 7-fold in increasing order of Cl- < SO4(2-) < HCO3- < HPO4(2). This order is consistent with their affinity to form complexes with iron oxide. Nitrate, a NZVI-reducible groundwater solute, present at 0.2 and 1 mN did not affect the rate of TCE reduction but increased acetylene production and decreased H2 evolution. NO3- present at > 3 mM slowed TCE dechlorination due to surface passivation. NO3- present at 5 mM stopped TCE dechlorination and H2 evolution after 3 days. <span class="hlt">Dissolved</span> solutes accounted for the observed decrease of NZVI reactivity for TCE dechlorination in natural groundwater when the total organic content was small (< 1 mg/L).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29749182','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29749182"><span>[Effects of nitrogen deposition on the <span class="hlt">concentration</span> and spectral characteristics of <span class="hlt">dissolved</span> organic matter in soil solution in a young Cunninghamia lanceolata plantation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yuan, Xiao Chun; Chen, Yue Min; Yuan, Shuo; Zheng, Wei; Si, You Tao; Yuan, Zhi Peng; Lin, Wei Sheng; Yang, Yu Sheng</p> <p>2017-01-01</p> <p>To study the effects of nitrogen deposition on the <span class="hlt">concentration</span> and spectral characteristics of <span class="hlt">dissolved</span> organic matter (DOM) in the forest soil solution from the subtropical Cunninghamia lanceolata plantation, using negative pressure sampling method, the dynamics of DOM in soil solutions from 0-15 and 15-30 cm soil layer was monitored for two years and the spectroscopic features of DOM were analyzed. The results showed that nitrogen deposition significantly reduced the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> organic carbon (DOC), and increased the aromatic index (AI) and the humic index (HIX), but had no significant effect on <span class="hlt">dissolved</span> organic nitrogen (DON) <span class="hlt">concentration</span> in both soil layers. There was obvious seasonal variation in DOM <span class="hlt">concentration</span> of the soil solution, which was prominently higher in summer and autumn than in spring and winter.Fourier-transform infrared (FTIR) absorption spectrometry indicated that the DOM in forest soil solution had absorption peaks in the similar position of six regions, being the highest in wave number of 1145-1149 cm -1 . Three-dimensional fluorescence spectra indicated that DOM was mainly consisted of protein-like substances (Ex/Em=230 nm/300 nm) and microbial degradation products (Ex/Em=275 nm/300 nm). The availability of protein-like substances from 0-15 cm soil layer was reduced in the nitrogen treatments. Nitrogen deposition significantly reduced the <span class="hlt">concentration</span> of DOC in soil solution, maybe largely by reducing soil pH, inhibiting soil carbon mineralization and stimulating plant growth. In particular, the decline of DOC <span class="hlt">concentration</span> in the surface layer was due to the production inhibition of the protein-like substances and carboxylic acids. Short-term nitrogen deposition might be beneficial to the maintenance of soil fertility, while the long-term accumulation of nitrogen deposition might lead to the hard utilization of soil nutrients.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3941031','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3941031"><span>Distribution of pyrethroid insecticides in secondary wastewater effluent</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Parry, Emily; Young, Thomas M.</p> <p>2014-01-01</p> <p>Although the <span class="hlt">freely</span> <span class="hlt">dissolved</span> form of hydrophobic organic chemicals may best predict aquatic toxicity, differentiating between <span class="hlt">dissolved</span> and particle bound forms is challenging at environmentally relevant <span class="hlt">concentrations</span> for compounds with low toxicity thresholds such as pyrethroid insecticides. We investigated the distribution of pyrethroids among three forms: <span class="hlt">freely</span> <span class="hlt">dissolved</span>, complexed with <span class="hlt">dissolved</span> organic carbon (DOC), and sorbed to suspended particulate matter, during a yearlong study at a secondary wastewater treatment plant. Effluent was fractionated by laboratory centrifugation to determine if sorption was driven by particle size. Linear distribution coefficients were estimated for pyrethroid sorption to suspended particulate matter (Kid) and <span class="hlt">dissolved</span> organic carbon (Kidoc) at environmentally relevant pyrethroid <span class="hlt">concentrations</span>. Resulting Kid values were higher than those reported for other environmental solids, and variation between sampling events correlated well with available particle surface area. Fractionation results suggest that no more than 40% of the pyrethroid remaining in secondary effluent could be removed by extending settling periods. Less than 6%of the total pyrethroid load in wastewater effluent was present in the <span class="hlt">dissolved</span> form across all sampling events and chemicals. PMID:23939863</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25576130','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25576130"><span>Variations in <span class="hlt">dissolved</span> organic nitrogen <span class="hlt">concentration</span> in biofilters with different media during drinking water treatment.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Huining; Zhang, Kefeng; Jin, Huixia; Gu, Li; Yu, Xin</p> <p>2015-11-01</p> <p><span class="hlt">Dissolved</span> organic nitrogen (DON) is potential precursor of disinfection byproducts (DBPs), especially nitrogenous DBPs. In this study, we investigated the impact of biofilters on DON <span class="hlt">concentration</span> changes in a drinking water plant. A small pilot plant was constructed next to a sedimentation tank in a drinking water plant and included activated carbon, quartz sand, anthracite, and ceramsite biofilters. As the biofilter layer depth increased, the DON <span class="hlt">concentration</span> first decreased and then increased, and the variation in DON <span class="hlt">concentration</span> differed among the biofilters. In the activated carbon biofilter, the DON <span class="hlt">concentration</span> was reduced by the largest amount in the first part of the column and increased by the largest amount in the second part of the column. The biomass in the activated carbon filter was less than that in the quartz sand filter in the upper column. The heterotrophic bacterial proportion among bacterial flora in the activated carbon biofilter was the largest, which might be due to the significant reduction in DON in the first part of the column. Overall, the results indicate that the DON <span class="hlt">concentration</span> in biofiltered water can be controlled via the selection of appropriate biofilter media. We propose that a two-layer biofilter with activated carbon in the upper layer and another media type in the lower layer could best reduce the DON <span class="hlt">concentration</span>. Copyright © 2014 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1392303-freely-tunable-broadband-polarization-rotator-terahertz-waves','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1392303-freely-tunable-broadband-polarization-rotator-terahertz-waves"><span><span class="hlt">Freely</span> Tunable Broadband Polarization Rotator for Terahertz Waves</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Fan, Ren-Hao; Zhou, Yu; Ren, Xiao-Ping</p> <p>2014-12-28</p> <p>A <span class="hlt">freely</span> tunable polarization rotator for broadband terahertz waves is demonstrated using a three-rotating-layer metallic grating structure, which can conveniently rotate the polarization of a linearly polarized terahertz wave to any desired direction with nearly perfect conversion efficiency. This low-cost, high-efficiency, and <span class="hlt">freely</span> tunable device has potential applications as material analysis, wireless communication, and THz imaging.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1022069','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1022069"><span>ADDING REALISM TO NUCLEAR MATERIAL <span class="hlt">DISSOLVING</span> ANALYSIS</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Williamson, B.</p> <p>2011-08-15</p> <p>Two new criticality modeling approaches have greatly increased the efficiency of <span class="hlt">dissolver</span> operations in H-Canyon. The first new approach takes credit for the linear, physical distribution of the mass throughout the entire length of the fuel assembly. This distribution of mass is referred to as the linear density. Crediting the linear density of the fuel bundles results in using lower fissile <span class="hlt">concentrations</span>, which allows higher masses to be charged to the <span class="hlt">dissolver</span>. Also, this approach takes credit for the fact that only part of the fissile mass is wetted at a time. There are multiple assemblies stacked on top ofmore » each other in a bundle. On average, only 50-75% of the mass (the bottom two or three assemblies) is wetted at a time. This means that only 50-75% (depending on operating level) of the mass is moderated and is contributing to the reactivity of the system. The second new approach takes credit for the progression of the <span class="hlt">dissolving</span> process. Previously, <span class="hlt">dissolving</span> analysis looked at a snapshot in time where the same fissile material existed both in the wells and in the bulk solution at the same time. The second new approach models multiple consecutive phases that simulate the fissile material moving from a high <span class="hlt">concentration</span> in the wells to a low <span class="hlt">concentration</span> in the bulk solution. This approach is more realistic and allows higher fissile masses to be charged to the <span class="hlt">dissolver</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3727121','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3727121"><span>Characterization of Urban Runoff Pollution between <span class="hlt">Dissolved</span> and Particulate Phases</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Wei, Zhang; Simin, Li; Fengbing, Tang</p> <p>2013-01-01</p> <p>To develop urban stormwater management effectively, characterization of urban runoff pollution between <span class="hlt">dissolved</span> and particulate phases was studied by 12 rainfall events monitored for five typical urban catchments. The average event mean <span class="hlt">concentration</span> (AEMC) of runoff pollutants in different phases was evaluated. The AEMC values of runoff pollutants in different phases from urban roads were higher than the ones from urban roofs. The proportions of total <span class="hlt">dissolved</span> solids, total <span class="hlt">dissolved</span> nitrogen, and total <span class="hlt">dissolved</span> phosphorus in total ones for all the catchments were 26.19%–30.91%, 83.29%–90.51%, and 61.54–68.09%, respectively. During rainfall events, the pollutant <span class="hlt">concentration</span> at the initial stage of rainfall was high and then sharply decreased to a low value. Affected by catchments characterization and rainfall distribution, the highest <span class="hlt">concentration</span> of road pollutants might appear in the later period of rainfall. Strong correlations were also found among runoffs pollutants in different phases. Total suspended solid could be considered as a surrogate for particulate matters in both road and roof runoff, while <span class="hlt">dissolved</span> chemical oxygen demand could be regarded as a surrogate for <span class="hlt">dissolved</span> matters in roof runoff. PMID:23935444</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23935444','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23935444"><span>Characterization of urban runoff pollution between <span class="hlt">dissolved</span> and particulate phases.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wei, Zhang; Simin, Li; Fengbing, Tang</p> <p>2013-01-01</p> <p>To develop urban stormwater management effectively, characterization of urban runoff pollution between <span class="hlt">dissolved</span> and particulate phases was studied by 12 rainfall events monitored for five typical urban catchments. The average event mean <span class="hlt">concentration</span> (AEMC) of runoff pollutants in different phases was evaluated. The AEMC values of runoff pollutants in different phases from urban roads were higher than the ones from urban roofs. The proportions of total <span class="hlt">dissolved</span> solids, total <span class="hlt">dissolved</span> nitrogen, and total <span class="hlt">dissolved</span> phosphorus in total ones for all the catchments were 26.19%-30.91%, 83.29%-90.51%, and 61.54-68.09%, respectively. During rainfall events, the pollutant <span class="hlt">concentration</span> at the initial stage of rainfall was high and then sharply decreased to a low value. Affected by catchments characterization and rainfall distribution, the highest <span class="hlt">concentration</span> of road pollutants might appear in the later period of rainfall. Strong correlations were also found among runoffs pollutants in different phases. Total suspended solid could be considered as a surrogate for particulate matters in both road and roof runoff, while <span class="hlt">dissolved</span> chemical oxygen demand could be regarded as a surrogate for <span class="hlt">dissolved</span> matters in roof runoff.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/19547','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/19547"><span>Sources, transformations, and hydrological processes that control stream nitrate and <span class="hlt">dissolved</span> organic matter <span class="hlt">concentrations</span> during snowmelt in an upland forest</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Stephen D. Sebestyen; Elizabeth W. Boyer; James B. Shanley; Carol Kendall; Daniel H. Doctor; George R. Aiken; Nobuhito Ohte</p> <p>2008-01-01</p> <p>We explored catchment processes that control stream nutrient <span class="hlt">concentrations</span> at an upland forest in northeastern Vermont, USA, where inputs of nitrogen via atmospheric deposition are among the highest in the nation and affect ecosystem functioning. We traced sources of water, nitrate, and <span class="hlt">dissolved</span> organic matter (DOM) using stream water samples collected at high...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24995476','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24995476"><span>A <span class="hlt">freely</span>-moving monkey treadmill model.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Foster, Justin D; Nuyujukian, Paul; Freifeld, Oren; Gao, Hua; Walker, Ross; I Ryu, Stephen; H Meng, Teresa; Murmann, Boris; J Black, Michael; Shenoy, Krishna V</p> <p>2014-08-01</p> <p>Motor neuroscience and brain-machine interface (BMI) design is based on examining how the brain controls voluntary movement, typically by recording neural activity and behavior from animal models. Recording technologies used with these animal models have traditionally limited the range of behaviors that can be studied, and thus the generality of science and engineering research. We aim to design a <span class="hlt">freely</span>-moving animal model using neural and behavioral recording technologies that do not constrain movement. We have established a <span class="hlt">freely</span>-moving rhesus monkey model employing technology that transmits neural activity from an intracortical array using a head-mounted device and records behavior through computer vision using markerless motion capture. We demonstrate the flexibility and utility of this new monkey model, including the first recordings from motor cortex while rhesus monkeys walk quadrupedally on a treadmill. Using this monkey model, we show that multi-unit threshold-crossing neural activity encodes the phase of walking and that the average firing rate of the threshold crossings covaries with the speed of individual steps. On a population level, we find that neural state-space trajectories of walking at different speeds have similar rotational dynamics in some dimensions that evolve at the step rate of walking, yet robustly separate by speed in other state-space dimensions. <span class="hlt">Freely</span>-moving animal models may allow neuroscientists to examine a wider range of behaviors and can provide a flexible experimental paradigm for examining the neural mechanisms that underlie movement generation across behaviors and environments. For BMIs, <span class="hlt">freely</span>-moving animal models have the potential to aid prosthetic design by examining how neural encoding changes with posture, environment and other real-world context changes. Understanding this new realm of behavior in more naturalistic settings is essential for overall progress of basic motor neuroscience and for the successful</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JNEng..11d6020F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JNEng..11d6020F"><span>A <span class="hlt">freely</span>-moving monkey treadmill model</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Foster, Justin D.; Nuyujukian, Paul; Freifeld, Oren; Gao, Hua; Walker, Ross; Ryu, Stephen I.; Meng, Teresa H.; Murmann, Boris; Black, Michael J.; Shenoy, Krishna V.</p> <p>2014-08-01</p> <p>Objective. Motor neuroscience and brain-machine interface (BMI) design is based on examining how the brain controls voluntary movement, typically by recording neural activity and behavior from animal models. Recording technologies used with these animal models have traditionally limited the range of behaviors that can be studied, and thus the generality of science and engineering research. We aim to design a <span class="hlt">freely</span>-moving animal model using neural and behavioral recording technologies that do not constrain movement. Approach. We have established a <span class="hlt">freely</span>-moving rhesus monkey model employing technology that transmits neural activity from an intracortical array using a head-mounted device and records behavior through computer vision using markerless motion capture. We demonstrate the flexibility and utility of this new monkey model, including the first recordings from motor cortex while rhesus monkeys walk quadrupedally on a treadmill. Main results. Using this monkey model, we show that multi-unit threshold-crossing neural activity encodes the phase of walking and that the average firing rate of the threshold crossings covaries with the speed of individual steps. On a population level, we find that neural state-space trajectories of walking at different speeds have similar rotational dynamics in some dimensions that evolve at the step rate of walking, yet robustly separate by speed in other state-space dimensions. Significance. <span class="hlt">Freely</span>-moving animal models may allow neuroscientists to examine a wider range of behaviors and can provide a flexible experimental paradigm for examining the neural mechanisms that underlie movement generation across behaviors and environments. For BMIs, <span class="hlt">freely</span>-moving animal models have the potential to aid prosthetic design by examining how neural encoding changes with posture, environment and other real-world context changes. Understanding this new realm of behavior in more naturalistic settings is essential for overall progress of basic</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26925752','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26925752"><span>Bioconcentration of perfluoroalkyl substances by Chironomus plumosus larvae in water with different types of <span class="hlt">dissolved</span> organic matters.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wen, Wu; Xia, Xinghui; Chen, Xi; Wang, Haotian; Zhu, Baotong; Li, Husheng; Li, Yang</p> <p>2016-06-01</p> <p>The effects of four types of <span class="hlt">dissolved</span> organic matters (DOM) on the bioconcentration of perfluoroalkyl substances (PFASs) in Chironomus plumosus larvae have been studied. The PFASs included perfluorooctane sulfonate (PFOS), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), perfluorodecanoic acid (PFDA), perfluoroundecanoic acid (PFUnA), and perfluorododecanoic acid (PFDoA). The DOM included humic acid (HA), fulvic acid (FA), tannic acid (TA), and a protein, peptone (PEP), and their <span class="hlt">concentrations</span> ranged from 0 to 50 mg L(-1). The results showed that, upon bioconcentration equilibrium, the body burdens of longer perfluoroalkyl chain PFASs (PFOS, PFDA, PFUnA and PFDoA) decreased with PEP and HA <span class="hlt">concentrations</span> while increased with FA and TA <span class="hlt">concentrations</span>. When FA and TA <span class="hlt">concentrations</span> increased from 0 to 50 mg L(-1), body burdens of these PFASs increased by 7.5%-148.8% and 5.7%-37.1%, respectively. However, the DOM had no significant impact on the body burdens of shorter perfluoroalkyl chain PFASs (PFOA and PFNA). All of the four types of DOM lowered not only the uptake rate constants (ku) of PFASs due to the decrease of <span class="hlt">freely</span> <span class="hlt">dissolved</span> PFAS <span class="hlt">concentrations</span>, but also the elimination rate constants (ke) due to the inhibition effect of DOM on the PFAS elimination from the larvae. The reduction in the two constants varied with both DOM and PFAS types. In the presence of PEP and HA with larger molecular weights, the ku values decreased more than ke, leading to the decreased body burdens of longer perfluoroalkyl chain PFASs. As for FA and TA with smaller molecular weights, the ke values decreased more than ku, resulting in increased body burdens of longer perfluoroalkyl chain PFASs. This study suggests that the effects of DOM on PFAS bioconcentration depend not only on the <span class="hlt">concentration</span> but also on the molecule weight of DOM, which should be considered in the bioavailability assessment of PFASs. Copyright © 2016 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70161733','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70161733"><span>Lake transparency: a window into decadal variations in <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> in Lakes of Acadia National Park, Maine</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Roesler, Collin S.; Culbertson, Charles W.</p> <p>2016-01-01</p> <p>A forty year time series of Secchi depth observations from approximately 25 lakes in Acadia National Park, Maine, USA, evidences large variations in transparency between lakes but relatively little seasonal cycle within lakes. However, there are coherent patterns over the time series, suggesting large scale processes are responsible. It has been suggested that variations in colored <span class="hlt">dissolved</span> organic matter (CDOM) are primarily responsible for the variations in transparency, both between lakes and over time and further that CDOM is a robust optical proxy for <span class="hlt">dissolved</span> organic carbon (DOC). Here we present a forward model of Secchi depth as a function of DOC based upon first principles and bio-optical relationships. Inverting the model to estimate DOC <span class="hlt">concentration</span> from Secchi depth observations compared well with the measured DOC <span class="hlt">concentrations</span> collected since 1995 (RMS error < 1.3 mg C l-1). This inverse model allows the time series of DOC to be extended back to the mid 1970s when only Secchi depth observations were collected, and thus provides a means for investigating lake response to climate forcing, changing atmospheric chemistry and watershed characteristics, including land cover and land use.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24862001','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24862001"><span>Effects of inoculum type and bulk <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on achieving partial nitrification by entrapped-cell-based reactors.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rongsayamanont, Chaiwat; Limpiyakorn, Tawan; Khan, Eakalak</p> <p>2014-07-01</p> <p>An entrapment of nitrifiers into gel matrix is employed as a tool to fulfill partial nitrification under non-limiting <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentrations</span> in bulk solutions. This study aims to clarify which of these two attributes, inoculum type and DO <span class="hlt">concentration</span> in bulk solutions, is the decisive factor for partial nitrification in an entrapped-cell based system. Four polyvinyl alcohol entrapped inocula were prepared to have different proportions of nitrite-oxidizing bacteria (NOB) and nitrite-oxidizing activity. At a DO <span class="hlt">concentration</span> of 3 mg l(-1), the number of active NOB cells in an inoculum was the decisive factor for partial nitrification enhancement. However, when the DO <span class="hlt">concentration</span> was reduced to 2 mg l(-1), all entrapped cell inocula showed similar degrees of partial nitrification. The results suggested that with the lower bulk DO <span class="hlt">concentration</span>, the preparation of entrapped cell inocula is not useful as the DO level becomes the decisive factor for achieving partial nitrification. Copyright © 2014 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/wri034177/pdf/wri034177.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/wri034177/pdf/wri034177.pdf"><span>Water temperature, specific conductance, pH, and <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> in the lower White River and the Puyallup River estuary, Washington, August-October 2002</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Ebbert, James C.</p> <p>2003-01-01</p> <p>The U.S. Geological Survey, Washington State Department of Ecology, and Puyallup Tribe of Indians monitored water temperature, specific conductance, pH, and <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> in the White River at river miles 4.9 and 1.8 from August until mid-October 2002. Water diverted from the White River upstream from the monitoring sites into Lake Tapps is returned to the river at river mile 3.6 between the two sites. The same characteristics were measured in a cross section of the Puyallup River estuary at river mile 1.5 during high and low tides in September 2002. In late August, maximum daily water temperatures in the White River of 21.1°C (degrees Celsius) at river mile 4.9 and 19.6°C at river mile 1.8 exceeded the water-quality standard of 18°C at both monitoring sites. In mid-September, maximum daily water temperatures at river mile 4.9 exceeded the standard on 5 days. From August 2-25, water temperatures at both monitoring sites were similar and little or no water was discharged from Lake Tapps to the White River. Increases in water temperature at river mile 1.8 in late September and early October were caused by the mixing of warmer water discharged from Lake Tapps with cooler water in the White River.Specific conductance in the White River usually was lower at river mile 1.8 than at river mile 4.9 because of mixing with water from Lake Tapps, which has a lower specific conductance. Maximum values of pH in the White River at river mile 4.9 often exceeded the upper limit of the water-quality standard, 8.5 pH units, from early September until mid-October, when turbidity decreased. The pH standard was not exceeded at river mile 1.8. <span class="hlt">Dissolved</span>-oxygen <span class="hlt">concentrations</span> in the White River were often lower at river mile 1.8 than at river mile 4.9 because of mixing with water discharged from Lake Tapps, which has lower <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span>. The lowest <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen observed was 7.9 mg/L (milligrams per liter) at river mile 1.8. The</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/355590-effects-quantity-quality-contact-time-dissolved-organic-matter-bioconcentration-benzo-pyrene-nematode-caenorhabditis-elegans','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/355590-effects-quantity-quality-contact-time-dissolved-organic-matter-bioconcentration-benzo-pyrene-nematode-caenorhabditis-elegans"><span>Effects of quantity, quality, and contact time of <span class="hlt">dissolved</span> organic matter on bioconcentration of benzo[a]pyrene in the nematode Caenorhabditis elegans</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Haitzer, M.; Hoess, S.; Burnison, B.K.</p> <p>1999-03-01</p> <p>Quantity and quality of <span class="hlt">dissolved</span> organic matter (DOM) and the time allowed for DOM to interact with organic contaminants can influence their bioavailability. The authors studied the effect of natural aquatic DOM that had been in contact with benzo[a]pyrene (B[a]P) for 1 to 12 d on the bioconcentration of B[a]P in the nematode Caenorhabditis elegans. <span class="hlt">Dissolved</span> organic matter quality and quantity was varied by using DOM from three different sources, each in three different <span class="hlt">concentrations</span>. A model, based on the assumption that only <span class="hlt">freely</span> <span class="hlt">dissolved</span> B[a]P is bioavailable, was employed to estimate biologically determined partition coefficients [K{sub p}(biol.)]. Expressing themore » data for each combination of DOM source and contact time in a single K{sub p} (biol.) value allowed a direct comparison of the effects of different DOM qualities and contact times. The results show that the effect of DOM from a specific source was dependent on DOM quantity, but they also observed a distinct effect of DOM quality (represented by different sampling locations) on the bioconcentration of B[a]P. Contact time had no significant influence for the effects of two DOM sources on the bioconcentration of B[a]P. However, the third DOM source was significantly more effective with increased contact time, leading to lower B[a]P bioconcentration in the nematodes.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010ECSS...88...12Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010ECSS...88...12Y"><span>Distributions and seasonal variations of <span class="hlt">dissolved</span> carbohydrates in the Jiaozhou Bay, China</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yang, Gui-Peng; Zhang, Yan-Ping; Lu, Xiao-Lan; Ding, Hai-Bing</p> <p>2010-06-01</p> <p>Surface seawater samples were collected in the Jiaozhou Bay, a typical semi-closed basin located at the western part of the Shandong Peninsula, China, during four cruises. <span class="hlt">Concentrations</span> of monosaccharides (MCHO), polysaccharides (PCHO) and total <span class="hlt">dissolved</span> carbohydrates (TCHO) were measured with the 2,4,6-tripyridyl- s-triazine spectroscopic method. <span class="hlt">Concentrations</span> of TCHO varied from 10.8 to 276.1 μM C for all samples and the ratios of TCHO to <span class="hlt">dissolved</span> organic carbon (DOC) ranged from 1.1 to 67.9% with an average of 10.1%. This result indicated that <span class="hlt">dissolved</span> carbohydrates were an important constituent of DOC in the surface seawater of the Jiaozhou Bay. In all samples, the <span class="hlt">concentrations</span> of MCHO ranged from 2.9 to 65.9 μM C, comprising 46.1 ± 16.6% of TCHO on average, while PCHO ranged from 0.3 to 210.2 μM C, comprising 53.9 ± 16.6% of TCHO on average. As a major part of <span class="hlt">dissolved</span> carbohydrates, the <span class="hlt">concentrations</span> of PCHO were higher than those of MCHO. MCHO and PCHO accumulated in January and July, with minimum average <span class="hlt">concentration</span> in April. The seasonal variation in the ratios of TCHO to DOC was related to water temperature, with high values in January and low values in July and October. The <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> carbohydrates displayed a decreasing trend from the coastal to the central areas. Negative correlations between <span class="hlt">concentrations</span> of TCHO and salinity in July suggested that riverine input around the Jiaozhou Bay had an important effect on the <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> carbohydrates in surface seawater. The pattern of distributions of MCHO and PCHO reported in this study added to the global picture of <span class="hlt">dissolved</span> carbohydrates distribution.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/15617436','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/15617436"><span>Effect of temperature and <span class="hlt">dissolved</span> oxygen on biological nitrification at high ammonia <span class="hlt">concentrations</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Weon, S Y; Lee, S I; Koopman, B</p> <p>2004-11-01</p> <p>Effect of temperature and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on nitrification rate were investigated with enrichment cultures of nitrifying bacteria. Values of specific nitrite oxidation rate in the absence of ammonia were 2.9-12 times higher than maximum specific ammonia oxidation rates at the same temperatures. The presence of high ammonia levels reversed this relationship, causing maximum specific nitrite oxidation rates to fall to 19 to 45% as high as maximum specific ammonia oxidation rates. This result suggests that nitrification at high ammonia levels will invariably result in nitrite accumulation. The K(O2) for nitrite oxidation in the presence of high ammonia levels was higher than the K(O2) for ammonia oxidation when temperature exceeded 18 degrees C, whereas the opposite was true at lower temperatures. These results indicate that low oxygen tensions will exacerbate nitrite accumulation when water temperature is high.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2006/5315/sir2006-5315.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2006/5315/sir2006-5315.pdf"><span><span class="hlt">Dissolved</span> solids in basin-fill aquifers and streams in the southwestern United States</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Anning, David W.; Bauch, Nancy J.; Gerner, Steven J.; Flynn, Marilyn E.; Hamlin, Scott N.; Moore, Stephanie J.; Schaefer, Donald H.; Anderholm, Scott K.; Spangler, Lawrence E.</p> <p>2007-01-01</p> <p>The U.S. Geological Survey National Water-Quality Assessment Program performed a regional study in the Southwestern United States (Southwest) to describe the status and trends of <span class="hlt">dissolved</span> solids in basin-fill aquifers and streams and to determine the natural and human factors that affect <span class="hlt">dissolved</span> solids. Basin-fill aquifers, which include the Rio Grande aquifer system, Basin and Range basin-fill aquifers, and California Coastal Basin aquifers, are the most extensively used ground-water supplies in the Southwest. Rivers, such as the Colorado, the Rio Grande, and their tributaries, are also important water supplies, as are several smaller river systems that drain internally within the Southwest, or drain externally to the Pacific Ocean in southern California. The study included four components that characterize (1) the spatial distribution of <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> in basin-fill aquifers, and <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>, loads, and yields in streams; (2) natural and human factors that affect <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>; (3) major sources and areas of accumulation of <span class="hlt">dissolved</span> solids; and (4) trends in <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> over time in basin-fill aquifers and streams, and the relation of trends to natural or human factors.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li class="active"><span>8</span></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_8 --> <div id="page_9" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li class="active"><span>9</span></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="161"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011GeoRL..38.8605Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011GeoRL..38.8605Z"><span>In situ Raman-based measurements of high <span class="hlt">dissolved</span> methane <span class="hlt">concentrations</span> in hydrate-rich ocean sediments</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhang, Xin; Hester, Keith C.; Ussler, William; Walz, Peter M.; Peltzer, Edward T.; Brewer, Peter G.</p> <p>2011-04-01</p> <p>Ocean sediment <span class="hlt">dissolved</span> CH4 <span class="hlt">concentrations</span> are of interest for possible climate-driven venting from sea floor hydrate decomposition, for supporting the large-scale microbial anaerobic oxidation of CH4 that holds the oceanic CH4 budget in balance, and for environmental issues of the oil and gas industry. Analyses of CH4 from recovered cores near vent locations typically show a maximum of ˜1 mM, close to the 1 atmosphere equilibrium value. We show from novel in situ measurement with a Raman-based probe that geochemically coherent profiles of <span class="hlt">dissolved</span> CH4 occur rising to 30 mM (pCH4 = 3 MPa) or an excess pressure ˜3× greater than CO2 in a bottle of champagne. Normalization of the CH4 Raman ν1 peak to the ubiquitous water ν2 bending peak provides a fundamental internal calibration. Very large losses of CH4 and fractions of other gases (CO2, H2S) must typically occur from recovered cores at gas rich sites. The new data are consistent with observations of microbial biomass and observed CH4 oxidation rates at hydrate rich sites and support estimates of a greatly expanded near surface oceanic pore water CH4 reservoir.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/4336131','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/biblio/4336131"><span>METHOD OF <span class="hlt">DISSOLVING</span> URANIUM METAL</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Slotin, L.A.</p> <p>1958-02-18</p> <p>This patent relates to an economicai means of <span class="hlt">dissolving</span> metallic uranium. It has been found that the addition of a small amount of perchloric acid to the <span class="hlt">concentrated</span> nitric acid in which the uranium is being <span class="hlt">dissolved</span> greatly shortens the time necessary for dissolution of the metal. Thus the use of about 1 or 2 percent of perchioric acid based on the weight of the nitric acid used, reduces the time of dissolution of uranium by a factor of about 100.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25019318','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25019318"><span>Spatial trends, sources, and air-water exchange of organochlorine pesticides in the Great Lakes basin using low density polyethylene passive samplers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Khairy, Mohammed; Muir, Derek; Teixeira, Camilla; Lohmann, Rainer</p> <p>2014-08-19</p> <p>Polyethylene passive samplers were deployed during summer and fall of 2011 in the lower Great Lakes to assess the spatial distribution and sources of gaseous and <span class="hlt">freely</span> <span class="hlt">dissolved</span> organochlorine pesticides (OCPs) and their air-water exchange. Average gaseous OCP <span class="hlt">concentrations</span> ranged from nondetect to 133 pg/m(3). Gaseous <span class="hlt">concentrations</span> of hexachlorobenzene, dieldrin, and chlordanes were significantly greater (Mann-Whitney test, p < 0.05) at Lake Erie than Lake Ontario. A multiple linear regression implied that both cropland and urban areas within 50 and 10 km buffer zones, respectively, were critical parameters to explain the total variability in atmospheric <span class="hlt">concentrations</span>. <span class="hlt">Freely</span> <span class="hlt">dissolved</span> OCP <span class="hlt">concentrations</span> (nondetect to 114 pg/L) were lower than previously reported. Aqueous half-lives generally ranged from 1.7 to 6.7 years. Nonetheless, <span class="hlt">concentrations</span> of p,p'-DDE and chlordanes were higher than New York State Ambient Water Quality Standards for the protection of human health from the consumption of fish. Spatial distributions of <span class="hlt">freely</span> <span class="hlt">dissolved</span> OCPs in both lakes were influenced by loadings from areas of concern and the water circulation patterns. Flux calculations indicated net deposition of γ-hexachlorocyclohexane, heptachlor-epoxide, and α- and β-endosulfan (-0.02 to -33 ng/m(2)/day) and net volatilization of heptachlor, aldrin, trans-chlordane, and trans-nonachlor (0.0 to 9.0 ng/m(2)/day) in most samples.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25929058','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25929058"><span>[Sources of <span class="hlt">dissolved</span> organic carbon and the bioavailability of <span class="hlt">dissolved</span> carbohydrates in the tributaries of Lake Taihu].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ye, Lin-Lin; Wu, Xiao-Dong; Kong, Fan-Xiang; Liu, Bo; Yan, De-Zhi</p> <p>2015-03-01</p> <p>Surface water samples of Yincungang and Chendonggang Rivers were collected from September 2012 to August 2013 in Lake Taihu. Water temperature, Chlorophyll a and bacterial abundance were analyzed, as well as <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentrations</span>, stable carbon isotope of DOC (Δ13C(DOC)), specific UV absorbance (SUVA254 ) and <span class="hlt">dissolved</span> carbohydrates <span class="hlt">concentrations</span>. Δ13C(DOC) ranged from -27.03% per thousand ± 0.30% per thousand to -23.38%per thousand ± 0.20% per thousand, indicating a terrestrial source. Both the autochthonous and allochthonous sources contributed to the carbohydrates pool in the tributaries. Significant differences in PCHO (polysaccharides) and MCHO (monosaccharides) <span class="hlt">concentrations</span> were observed between spring-summer and autumn-winter (P < 0.01, n = 12; P < 0.01, n = 12), which might be caused by the variation in the sources and bioavailability of carbohydrates. PCHO contributed a major fraction to TCHO (total <span class="hlt">dissolved</span> carbohydrates) in autumn and winter, which could be explained by the accumulation of undegradable PCHO limited by the low water temperature; MCHO contributed a major fraction to TCHO in spring and summer, which might be caused by the transformation from PCHO by microbes at high water temperature.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ECSS..180...82L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ECSS..180...82L"><span>Comparison of land-based sources with ambient estuarine <span class="hlt">concentrations</span> of total <span class="hlt">dissolved</span> nitrogen in Jiaozhou Bay (China)</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lu, Dongliang; Yang, Nannan; Liang, Shengkang; Li, Keqiang; Wang, Xiulin</p> <p>2016-10-01</p> <p>Seasonal, land-sea synchronous surveys were conducted from 2012 to 2013 to characterize the relationship between the composition of land-based total <span class="hlt">dissolved</span> nitrogen (TDN) and the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> inorganic nitrogen (DIN) in Jiaozhou Bay (JZB). A total of 11 freshwater riverine sampling sites were selected at the river mouths and at waste water outfalls around JZB, while a total 23 Bay stations were established in JZB. Among them, 11 Bay stations were located near the 11 outfalls. Each land-sea sampling was conducted synchronously during a semi-tidal cycle. The contribution of NO3sbnd N, NO2sbnd N, NH4sbnd N, and <span class="hlt">dissolved</span> organic nitrogen (DON) to TDN in land-based freshwater were similar to those in JZB seawater, while the contribution of the sum of NO3sbnd N and NO2sbnd N to TDN and the contribution of DON to TDN were about 3.2 and 4.1 times higher than the contribution of NH4sbnd N to TDN, respectively. These results showed that inputs of all land-based forms of nitrogen impact the DIN in seawater. Spatial distributions of DIN and DON, showing a gradual decrease from inner bay to the mouth of the bay, were negatively correlated with S in different seasons. In summer and winter, the ratio of DIN to DON in seawater (Rs) gradually decreased from the inner bay to the center of the bay, and the ratio of land-based DIN to DON (RL) was less than RS, indicating net transformation from land-based DON into marine DIN. However, in spring and autumn, the distribution of Rs was opposite to that in summer and winter, and RL was greater than RS, indicating net conversion from land-based DIN into marine DON. Throughout the whole year, net land-based DON was transformed into marine DIN. We provided direct evidence that the variation in DIN <span class="hlt">concentration</span> in JZB was affected both by land-based TDN inputs and by their hydrodynamic transport and biogeochemical transformation processes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70189351','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70189351"><span>Inorganic carbon loading as a primary driver of <span class="hlt">dissolved</span> carbon dioxide <span class="hlt">concentrations</span> in the lakes and reservoirs of the contiguous United States</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>McDonald, Cory P.; Stets, Edward; Striegl, Robert G.; Butman, David</p> <p>2013-01-01</p> <p>Accurate quantification of CO2 flux across the air-water interface and identification of the mechanisms driving CO2 <span class="hlt">concentrations</span> in lakes and reservoirs is critical to integrating aquatic systems into large-scale carbon budgets, and to predicting the response of these systems to changes in climate or terrestrial carbon cycling. Large-scale estimates of the role of lakes and reservoirs in the carbon cycle, however, typically must rely on aggregation of spatially and temporally inconsistent data from disparate sources. We performed a spatially comprehensive analysis of CO2 <span class="hlt">concentration</span> and air-water fluxes in lakes and reservoirs of the contiguous United States using large, consistent data sets, and modeled the relative contribution of inorganic and organic carbon loading to vertical CO2 fluxes. Approximately 70% of lakes and reservoirs are supersaturated with respect to the atmosphere during the summer (June–September). Although there is considerable interregional and intraregional variability, lakes and reservoirs represent a net source of CO2 to the atmosphere of approximately 40 Gg C d–1 during the summer. While in-lake CO2 <span class="hlt">concentrations</span> correlate with indicators of in-lake net ecosystem productivity, virtually no relationship exists between <span class="hlt">dissolved</span> organic carbon and pCO2,aq. Modeling suggests that hydrologic <span class="hlt">dissolved</span> inorganic carbon supports pCO2,aq in most supersaturated systems (to the extent that 12% of supersaturated systems simultaneously exhibit positive net ecosystem productivity), and also supports primary production in most CO2-undersaturated systems. <span class="hlt">Dissolved</span> inorganic carbon loading appears to be an important determinant of CO2<span class="hlt">concentrations</span> and fluxes across the air-water interface in the majority of lakes and reservoirs in the contiguous United States.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4906022','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4906022"><span>Supersaturation of <span class="hlt">Dissolved</span> Hydrogen and Methane in Rumen of Tibetan Sheep</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Wang, Min; Ungerfeld, Emilio M.; Wang, Rong; Zhou, Chuan She; Basang, Zhu Zha; Ao, Si Man; Tan, Zhi Liang</p> <p>2016-01-01</p> <p>Hydrogen (H2) is an essential substrate for methanogens to produce methane (CH4), and also influences pathways of volatile fatty acids (VFA) production in the rumen. <span class="hlt">Dissolved</span> H2 (H2 (aq)) is the form of H2 available to microbes, and <span class="hlt">dissolved</span> CH4 (CH4 (aq)) is important for indicating methanogens activity. Rumen H2 (aq) <span class="hlt">concentration</span> has been estimated by assuming equilibrium with headspace gaseous H2 (H2 (g)) <span class="hlt">concentration</span> using Henry's law, and has also been directly measured in the liquid phase in some in vitro and in vivo experiments. In this in vivo study, H2 (aq) and CH4 (aq) <span class="hlt">concentration</span> measured directly in rumen fluid and their corresponding <span class="hlt">concentrations</span> estimated from their gaseous phase <span class="hlt">concentrations</span>, were compared to investigate the existence of equilibrium between the gas and liquid phases. Twenty-four Tibetan sheep were randomly assigned to two mixed diets containing the same <span class="hlt">concentrate</span> mixed with oat grass (OG diet) or barley straw (BS diet). Rumen gaseous phase and contents were sampled using rumenocentesis and oral stomach tubing, respectively. Rumen H2 (aq) and CH4 (aq) <span class="hlt">concentration</span> and VFA profile differed between sheep fed OG and BS diets. Measured H2 (aq) and CH4 (aq) <span class="hlt">concentration</span> were greater than H2 (aq) and CH4 (aq) <span class="hlt">concentrations</span> estimated using gas <span class="hlt">concentrations</span>, indicating lack of equilibrium between gas and liquid phase and supersaturation of H2 and CH4 in rumen fluid. As a consequence, Gibbs energy changes (ΔG) estimated for various metabolic pathways were different when calculated using <span class="hlt">dissolved</span> gases <span class="hlt">concentrations</span> directly measured and when using <span class="hlt">dissolved</span> gases <span class="hlt">concentrations</span> assuming equilibrium with the gaseous phase. <span class="hlt">Dissolved</span> CH4, but not CH4 (g), was positively correlated with H2 (aq). Both H2 (aq) and H2 (g) <span class="hlt">concentrations</span> were positively correlated with the molar percentage of butyrate and negatively correlated with the molar percentage of acetate. In summary, rumen fluid was supersaturated with both H2 and CH4</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27506045','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27506045"><span>[Characteristics of <span class="hlt">Dissolved</span> CH₄ and N₂O <span class="hlt">Concentrations</span> of Weihe River in Xinxiang Section in Spring].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hou, Cui-cui; Zhang, Fang; Li, Ying-chen; Wang, Qi-bo; Liu, Sai</p> <p>2016-05-15</p> <p>Distributions of CH₄ and N₂O <span class="hlt">concentrations</span> in Weihe River in Xinxiang City were monitored in spring of 2015, and their influencing factors were discussed. The result showed that CH₄ and N₂O were super-saturated in surface water of Weihe River. The variation ranges of two gases' saturations in the surface water of Weihe River were 147.59-2667.85 (CH₄) and 4.06-188.25 (N₂O). In the urban area, significant correlation existed between N₂O and NH₄⁺-N <span class="hlt">concentrations</span> (P < 0.01), but in the new district, <span class="hlt">dissolved</span> N₂O <span class="hlt">concentration</span> showed sharp increase because of the water input from the urban sewage plants, illustrating that the controlling mechanism on N₂O production varied as pollutant characteristics changed. Stepwise regression analysis showed that CH₄ <span class="hlt">concentrations</span> could be explained by NH₄⁺-N <span class="hlt">concentrations</span> and water temperature, and CH₄ <span class="hlt">concentrations</span> in the surface water of Weihe River was significantly correlated with NH₄⁺-N <span class="hlt">concentrations</span> (R² = 0.70, P < 0.01), suggesting that NH₄⁺-N was the key factor in regulating the production and assumption of CH₄oxidation in Weihe River in spring. Besides, this study showed that when there was less NO₃⁻-N but more NH₄⁺-N in river water, CH₄and N₂O <span class="hlt">concentrations</span> would be positively correlated, indicating that different nitrogen sources would impact the coupling mechanism of CH₄and N₂O productions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017ExFl...58..164L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017ExFl...58..164L"><span>An experimental study on the cavitation of water with <span class="hlt">dissolved</span> gases</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Li, Buxuan; Gu, Youwei; Chen, Min</p> <p>2017-12-01</p> <p>Cavitation inception is generally determined by the tensile strengths of liquids. Investigations on the tensile strength of water, which is essential in many fields, will help understand the promotion/prevention of cavitation and related applications in water. Previous experimental studies, however, vary in their conclusions about the value of tensile strength of water; the difference is commonly attributed to the existence of impurities in water. <span class="hlt">Dissolved</span> gases, especially oxygen and nitrogen from the air, are one of the most common kinds of impurities in water. The influence of these gases on the tensile strength of water is still unclear. This study investigated the effects of <span class="hlt">dissolved</span> gases on water cavitation through experiments. Cavitation in water is generated by acoustic method. Water samples are prepared with <span class="hlt">dissolved</span> oxygen and nitrogen in different gas <span class="hlt">concentrations</span>. Results show that under the same temperature, the tensile strength of water with <span class="hlt">dissolved</span> oxygen or nitrogen decreases with increased gas <span class="hlt">concentration</span> compared with that of ultrapure water. Under the same gas <span class="hlt">concentration</span> and temperature, water with <span class="hlt">dissolved</span> oxygen shows a lower tensile strength than that with <span class="hlt">dissolved</span> nitrogen. Possible reasons of these results are also discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008E%26PSL.270..157B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008E%26PSL.270..157B"><span>The distribution and stabilisation of <span class="hlt">dissolved</span> Fe in deep-sea hydrothermal plumes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bennett, Sarah A.; Achterberg, Eric P.; Connelly, Douglas P.; Statham, Peter J.; Fones, Gary R.; German, Christopher R.</p> <p>2008-06-01</p> <p>We have conducted a study of hydrothermal plumes overlying the Mid-Atlantic Ridge near 5° S to investigate whether there is a significant export flux of <span class="hlt">dissolved</span> Fe from hydrothermal venting to the oceans. Our study combined measurements of plume-height Fe <span class="hlt">concentrations</span> from a series of 6 CTD stations together with studies of <span class="hlt">dissolved</span> Fe speciation in a subset of those samples. At 2.5 km down plume from the nearest known vent site <span class="hlt">dissolved</span> Fe <span class="hlt">concentrations</span> were ˜ 20 nM. This is much higher than would be predicted from a combination of plume dilution and <span class="hlt">dissolved</span> Fe(II) oxidation rates, but consistent with stabilisation due to the presence of organic Fe complexes and Fe colloids. Using Competitive Ligand Exchange-Cathodic Stripping Voltammetry (CLE-CSV), stabilised <span class="hlt">dissolved</span> Fe complexes were detected within the <span class="hlt">dissolved</span> Fe fraction on the edges of one non-buoyant hydrothermal plume with observed ligand <span class="hlt">concentrations</span> high enough to account for stabilisation of ˜ 4% of the total Fe emitted from the 5° S vent sites. If these results were representative of all hydrothermal systems, submarine venting could provide 12-22% of the global deep-ocean <span class="hlt">dissolved</span> Fe budget.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=dissolved+AND+oxygen+AND+concentrations&id=EJ095194','ERIC'); return false;" href="https://eric.ed.gov/?q=dissolved+AND+oxygen+AND+concentrations&id=EJ095194"><span>The Measurement of <span class="hlt">Dissolved</span> Oxygen</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Thistlethwayte, D.; And Others</p> <p>1974-01-01</p> <p>Describes an experiment in environmental chemistry which serves to determine the <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in both fresh and saline water. Applications of the method at the undergraduate and secondary school levels are recommended. (CC)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/of/1981/0479/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/of/1981/0479/report.pdf"><span>Documentation of a <span class="hlt">dissolved</span>-solids model of the Tongue River, southeastern Montana</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Woods, Paul F.</p> <p>1981-01-01</p> <p>A model has been developed for assessing potential increases in <span class="hlt">dissolved</span> solids of the Tongue River as a result of leaching of overburden materials used to backfill pits in surface coal-mining operations. The model allows spatial and temporal simulation of streamflow and <span class="hlt">dissolved</span>-solids loads and <span class="hlt">concentrations</span> under user-defined scenarios of surface coal mining and agricultural development. The model routes an input quantity of streamflow and <span class="hlt">dissolved</span> solids from the upstream end to the downstream end of a stream reach while algebraically accounting for gains and losses of streamflow and <span class="hlt">dissolved</span> solids within the stream reach. Input data needed to operate the model include the following: simulation number, designation of hydrologic conditions for each simulated month, either user-defined or regression-defined <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids input by the Tongue River Reservoir, number of irrigated acres, number of mined acres, <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> of mine leachates and quantity of other water losses. A listing of the Fortran computer program, definitions of all variables in the model, and an example output permit use of the model by interested persons. (USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014BGeo...11.3131M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014BGeo...11.3131M"><span>A synthesis of light absorption properties of the Arctic Ocean: application to semianalytical estimates of <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> from space</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Matsuoka, A.; Babin, M.; Doxaran, D.; Hooker, S. B.; Mitchell, B. G.; Bélanger, S.; Bricaud, A.</p> <p>2014-06-01</p> <p>In addition to scattering coefficients, the light absorption coefficients of particulate and <span class="hlt">dissolved</span> materials are the main factors determining the light propagation of the visible part of the spectrum and are, thus, important for developing ocean color algorithms. While these absorption properties have recently been documented by a few studies for the Arctic Ocean (e.g., Matsuoka et al., 2007, 2011; Ben Mustapha et al., 2012), the data sets used in the literature were sparse and individually insufficient to draw a general view of the basin-wide spatial and temporal variations in absorption. To achieve such a task, we built a large absorption database of the Arctic Ocean by pooling the majority of published data sets and merging new data sets. Our results show that the total nonwater absorption coefficients measured in the eastern Arctic Ocean (EAO; Siberian side) are significantly higher than in the western Arctic Ocean (WAO; North American side). This higher absorption is explained by higher <span class="hlt">concentration</span> of colored <span class="hlt">dissolved</span> organic matter (CDOM) in watersheds on the Siberian side, which contains a large amount of <span class="hlt">dissolved</span> organic carbon (DOC) compared to waters off North America. In contrast, the relationship between the phytoplankton absorption (aϕ(λ)) and chlorophyll a (chl a) <span class="hlt">concentration</span> in the EAO was not significantly different from that in the WAO. Because our semianalytical CDOM absorption algorithm is based on chl a-specific aϕ(λ) values (Matsuoka et al., 2013), this result indirectly suggests that CDOM absorption can be appropriately derived not only for the WAO but also for the EAO using ocean color data. Based on statistics, derived CDOM absorption values were reasonable compared to in situ measurements. By combining this algorithm with empirical DOC versus CDOM relationships, a semianalytical algorithm for estimating DOC <span class="hlt">concentrations</span> for river-influenced coastal waters of the Arctic Ocean is presented and applied to satellite</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/14703148','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/14703148"><span>Modelling of temperature effects on removal efficiency and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> in stormwater ponds.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>German, J; Svensson, G; Gustafsson, L G; Vikström, M</p> <p>2003-01-01</p> <p>The performance of stormwater ponds, operated under winter conditions, was modelled using the commercial software Mike21 and MOUSE. Direct and indirect effects of changing temperature were investigated. The most important effect of winter conditions is the changed hydrology, characterised by long periods with no runoff followed by snowmelt events with large runoff volumes during several days. This gives lower removal efficiencies than during a period with the same precipitation but without winter conditions. For the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen, wind is an important factor. Consequently the most important effect of an ice cover on the pond is that it prevents the oxygenation effects of the wind. The direct temperature effects on the removal processes are negligible compared to the indirect effects in changed hydrology and forming of ice cover.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015ApPhL.106s4107R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015ApPhL.106s4107R"><span>Single-molecule-sensitive fluorescence resonance energy transfer in <span class="hlt">freely</span>-diffusing attoliter droplets</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rahmanseresht, Sheema; Milas, Peker; Ramos, Kieran P.; Gamari, Ben D.; Goldner, Lori S.</p> <p>2015-05-01</p> <p>Fluorescence resonance energy transfer (FRET) from individual, dye-labeled RNA molecules confined in <span class="hlt">freely</span>-diffusing attoliter-volume aqueous droplets is carefully compared to FRET from unconfined RNA in solution. The use of <span class="hlt">freely</span>-diffusing droplets is a remarkably simple and high-throughput technique that facilitates a substantial increase in signal-to-noise for single-molecular-pair FRET measurements. We show that there can be dramatic differences between FRET in solution and in droplets, which we attribute primarily to an altered pH in the confining environment. We also demonstrate that a sufficient <span class="hlt">concentration</span> of a non-ionic surfactant mitigates this effect and restores FRET to its neutral-pH solution value. At low surfactant levels, even accounting for pH, we observe differences between the distribution of FRET values in solution and in droplets which remain unexplained. Our results will facilitate the use of nanoemulsion droplets as attoliter volume reactors for use in biophysical and biochemical assays, and also in applications such as protein crystallization or nanoparticle synthesis, where careful attention to the pH of the confined phase is required.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70175341','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70175341"><span>Experimental whole-lake increase of <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentration</span> produces unexpected increase in crustacean zooplankton density</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kelly, Patrick T.; Craig, Nicola; Solomon, Christopher T.; Weidel, Brian C.; Zwart, Jacob A.; Jones, Stuart E.</p> <p>2016-01-01</p> <p>The observed pattern of lake browning, or increased terrestrial <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentration</span>, across the northern hemisphere has amplified the importance of understanding how consumer productivity varies with DOC <span class="hlt">concentration</span>. Results from comparative studies suggest these increased DOC <span class="hlt">concentrations</span> may reduce crustacean zooplankton productivity due to reductions in resource quality and volume of suitable habitat. Although these spatial comparisons provide an expectation for the response of zooplankton productivity as DOC <span class="hlt">concentration</span> increases, we still have an incomplete understanding of how zooplankton respond to temporal increases in DOC <span class="hlt">concentration</span> within a single system. As such, we used a whole-lake manipulation, in which DOC <span class="hlt">concentration</span> was increased from 8 to 11 mg L−1 in one basin of a manipulated lake, to test the hypothesis that crustacean zooplankton production should subsequently decrease. In contrast to the spatially derived expectation of sharp DOC-mediated decline, we observed a small increase in zooplankton densities in response to our experimental increase in DOC <span class="hlt">concentration</span> of the treatment basin. This was due to significant increases in gross primary production and resource quality (lower seston carbon-to-phosphorus ratio; C:P). These results demonstrate that temporal changes in lake characteristics due to increased DOC may impact zooplankton in ways that differ from those observed in spatial surveys. We also identified significant interannual variability across our study region, which highlights potential difficulty in detecting temporal responses of organism abundances to gradual environmental change (e.g., browning).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/4130162','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/biblio/4130162"><span>METHOD OF <span class="hlt">DISSOLVING</span> MASSIVE PLUTONIUM</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Facer, J.F.; Lyon, W.L.</p> <p>1960-06-28</p> <p>Massive plutonium can be <span class="hlt">dissolved</span> in a hot mixture of <span class="hlt">concentrated</span> nitric acid and a small quantity of hydrofluoric acid. A preliminary oxidation with water under superatmospheric pressure at 140 to 150 deg C is advantageous</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.B51E0334S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.B51E0334S"><span>Influence of environmental parameters on the <span class="hlt">concentration</span> of subsurface <span class="hlt">dissolved</span> methane in two hydroelectric power plants in Brazil</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Silva, M. G.; Marani, L.; Alvala, P. C.</p> <p>2013-12-01</p> <p>Methane (CH4) is a trace gas in the atmosphere of great importance for atmospheric chemistry as one of the main greenhouse gases. There are different sources with the largest individual production associated with the degradation of organic matter submerged in flooded areas. The amount of <span class="hlt">dissolved</span> methane that reaches the surface depends on the production in the sediments and consumption in the water column. Both processes are associated with microbial activity and consequently dependent on the physico-chemical environmental conditions. The construction of hydroelectric dams cause flooding of areas near the river that can change the characteristics of the environment and cause changes in subsurface methane <span class="hlt">concentration</span>. In this work, we studied two hydroelectric plants located in Brazil: Batalha (17°20'39.52"S, 47°29'34.29"W), under construction when the samples were take, and Itaipu (25°24'45.00"S, 54°35'39.00"W) which has been floated over 30 years ago. The water samples to determine <span class="hlt">dissolved</span> methane were collected approximately 5 cm near the surface. In each collection point was measured depth, water temperature, pH and redox potential. The range of <span class="hlt">dissolved</span> methane between the two dams was similar: 0.07-10.33 μg/l (Batalha) and 0.15-10.93 μg/l (Itaipu). However, the Batalha's average (4.04 × 3.43 μg/l; median = 3.66 μg/l) was higher than that observed in Itaipu (2.15 × 1.59 μg/l; median = 2.53 μg/l). The influence of environmental parameters on the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> methane was evaluated by multivariate statistical techniques (Principal Component Analysis - PCA). All of the parameters had some correlation with <span class="hlt">dissolved</span> methane, however, the greatest contribution in Batalha was associated with pH while in Itaipu was the depth. The pH variation of the various points studied in Batalha may be associated with periods of drought and flooding of the river and hence the incorporation of organic matter in the environment. The organisms</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H41F1515L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H41F1515L"><span><span class="hlt">Dissolved</span> Greenhouse Gas <span class="hlt">Concentration</span> Patterns and Relationships with Stream Chemistry in Tropical Headwater Streams</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>López-Lloreda, C.; McDowell, W. H.; Potter, J.</p> <p>2017-12-01</p> <p>Recent studies have shown that freshwater ecosystems, mainly lakes and large rivers, can be an important source of greenhouse gas (GHG) emissions. Headwater streams have received less attention but have been identified as being a potentially important contributor to these emissions. The complex biogeochemical interactions between <span class="hlt">dissolved</span> GHG, stream chemistry and other physicochemical parameters in streams are not well understood, particularly in small, tropical headwater streams. Surface water samples were taken at weekly intervals at 8 sites in the Luquillo Experimental Forest in Puerto Rico. Samples were analyzed for carbon dioxide (CO2), methane (CH4) and nitrous oxide (N2O) as well as <span class="hlt">dissolved</span> organic carbon (DOC), nitrate (NO3) and other major cations and anions. Additionally, physicochemical parameters and discharge (at a subset of sites) were recorded for each sample. Initial analyses of stream greenhouse gas <span class="hlt">concentrations</span> showed very little seasonality across all sites as well as no change in <span class="hlt">concentrations</span> during a drought in 2015. One of our hypothesized drivers, discharge, did not show any significant relationship with any of the greenhouse gases at our two gaged sites. Relationships between GHG and stream chemistry, mainly DOC and NO3, varied across sites. A significant negative relationship was found between NO3 and N2O when data were pooled across all sites, but no significant relationship was found at any individual site. CH4 was positively correlated with NO3, but only at one of our sites. N2O showed a significant positive relationship with DOC at two of our sites but interestingly, CO2 and CH4 did not show any significant relationship with DOC. Our initial results suggest that NO3 can be an important driver for N2O and CH4 <span class="hlt">concentrations</span>, while DOC can be an important driver for N2O. Our results differ from those found in lowland tropical rivers, suggesting that river order and floodplain connections may be important drivers of GHG</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26648388','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26648388"><span><span class="hlt">Dissolved</span> oxygen <span class="hlt">concentration</span> in the medium during cell culture: Defects and improvements.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Kuan; Zhao, Tong; Huang, Xin; He, Yunlin; Zhou, Yanzhao; Wu, Liying; Wu, Kuiwu; Fan, Ming; Zhu, Lingling</p> <p>2016-03-01</p> <p>In vitro cell culture has provided a useful model to study the effects of oxygen on cellular behavior. However, it remains unknown whether the in vitro operations themselves affect the medium oxygen levels and the living states of cells. In addition, a prevailing controversy is whether reactive oxygen species (ROS) production is induced by continuous hypoxia or reoxygenation. In this study, we have measured the effects of different types of cell culture containers and the oxygen environment where medium replacement takes place on the actual oxygen tension in the medium. We found that the deviations of oxygen <span class="hlt">concentrations</span> in the medium are much greater in 25-cm(2) flasks than in 24-well plates and 35-mm dishes. The <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> in the medium were increased after medium replacement in normoxia, but remained unchanged in glove boxes in which the oxygen tension remained at a low level (11.4, 5.7, and 0.5% O2 ). We also found that medium replacement in normoxia increased the number of ROS-positive cells and reduced the cell viability; meanwhile, medium replacement in a glove box did not produce the above effects. Therefore, we conclude that the use of 25-cm(2) flasks should be avoided and demonstrate that continuous hypoxia does not produce ROS, whereas the reoxygenation that occurs during the harvesting of cells leads to ROS and induces cell death. © 2015 International Federation for Cell Biology.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li class="active"><span>9</span></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_9 --> <div id="page_10" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="181"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27332841','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27332841"><span>Leaching of <span class="hlt">dissolved</span> phosphorus from tile-drained agricultural areas.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Andersen, H E; Windolf, J; Kronvang, B</p> <p>2016-01-01</p> <p>We investigated leaching of <span class="hlt">dissolved</span> phosphorus (P) from 45 tile-drains representing animal husbandry farms in all regions of Denmark. Leaching of P via tile-drains exhibits a high degree of spatial heterogeneity with a low <span class="hlt">concentration</span> in the majority of tile-drains and few tile-drains (15% in our investigation) having high to very high <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> P. The share of <span class="hlt">dissolved</span> organic P (DOP) was high (up to 96%). Leaching of DOP has hitherto been a somewhat overlooked P loss pathway in Danish soils and the mechanisms of mobilization and transport of DOP needs more investigation. We found a high correlation between Olsen-P and water extractable P. Water extractable P is regarded as an indicator of risk of loss of <span class="hlt">dissolved</span> P. Our findings indicate that Olsen-P, which is measured routinely in Danish agricultural soils, may be a useful proxy for the P leaching potential of soils. However, we found no straight-forward correlation between leaching potential of the top soil layer (expressed as either degree of P saturation, Olsen-P or water extractable P) and the measured <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> P in the tile-drain. This underlines that not only the source of P but also the P loss pathway must be taken into account when evaluating the risk of P loss.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17681864','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17681864"><span>The effect of <span class="hlt">dissolve</span> gas <span class="hlt">concentration</span> in the initial growth stage of multi cavitation bubbles. Differences between vacuum degassing and ultrasound degassing.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yanagida, Hirotaka</p> <p>2008-04-01</p> <p>The sonochemical luminescence intensity from luminol was measured at a sampling rate of several kilohertz. This was noted at three different periods: first, the latent period in which no light emission occurs at all; second, the increased emission period from the start of light emission to the time when a steady state is reached; and third, the steady state period in which light emission occurs at the steady state value. When irradiated with ultrasound of different intensities, the times of the latent period and increased emission period are shorter for higher ultrasound intensities. To know how the <span class="hlt">dissolved</span> oxygen content is involved in early-stage cavitation growth, an experiment was conducted using solutions with varying <span class="hlt">dissolved</span> oxygen contents from 100% to 37%. For <span class="hlt">dissolved</span> air content of 50% or less, it was found that the latent period was 30 times longer in a saturated condition. It was also found that the increased emission period was 10 times longer. However, the emission intensity in the steady state did not change at all even when the initial <span class="hlt">dissolved</span> gas <span class="hlt">concentration</span> of the sample was changed. From this, it was found that the reuse of collapsed bubbles takes place efficiently in the steady state. <span class="hlt">Dissolved</span> oxygen was reduced by the use of a vacuum pump and by the degassing action of ultrasound, and it was discovered that the behavior of transient emission differed for the two ways of degassing.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=247634&keyword=information+AND+technology+AND+managers&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=247634&keyword=information+AND+technology+AND+managers&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Use of Passive Samplers to Measure <span class="hlt">Dissolved</span> Organic Contaminants in a Temperate Estuary</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Measuring <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> of organic contaminants can be challenging given their low solubilities and high particle association. However, to perform accurate risk assessments of these chemicals, knowing the <span class="hlt">dissolved</span> <span class="hlt">concentration</span> is critical since it is considered to b...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..19.8710D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..19.8710D"><span>Ancient <span class="hlt">dissolved</span> methane in inland waters at low <span class="hlt">concentrations</span> revealed by a new collection method for radiocarbon (^{14}C) analysis</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dean, Joshua F.; Billett, Michael F.; Murray, Callum; Garnett, Mark H.</p> <p>2017-04-01</p> <p>Methane (CH4) is a powerful greenhouse gas and is released to the atmosphere from freshwater systems in numerous biomes globally. Radiocarbon (14C) analysis of methane can provide unique information about its age, source and rate of cycling in natural environments. Methane is often released from aquatic sediments in bubbles (ebullition), but <span class="hlt">dissolved</span> methane is also present in lakes and streams at lower <span class="hlt">concentrations</span>, and may not be of the same age or source. Obtaining sufficient non-ebullitive aquatic methane for 14C analysis remains a major technical challenge. Previous studies have shown that freshwater methane, in both <span class="hlt">dissolved</span> and ebullitive form, can be significantly older than other forms of aquatic carbon (C), and it is therefore important to characterise this part of the terrestrial C balance. We present a novel method to capture sufficient amounts of <span class="hlt">dissolved</span> methane from freshwater environments for 14C analysis by circulating water across a hydrophobic, gas-permeable membrane and collecting the methane in a large collapsible vessel. The results of laboratory and field tests show that reliable <span class="hlt">dissolved</span> δ13CH4 and 14CH4 samples can be readily collected over short time periods (˜4 to 24 hours), at relatively low cost and from a variety of surface water types. The initial results further support previous findings that <span class="hlt">dissolved</span> methane can be significantly older than other forms of aquatic C, especially in organic-rich catchments, and is currently unaccounted for in many terrestrial C balances and models. This method is suitable for use in remote locations, and could potentially be used to detect the leakage of unique 14CH4 signatures from point sources into waterways, e.g. coal seam gas and landfill gas.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24037271','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24037271"><span>Development of mediator-type biosensor to wirelessly monitor whole cholesterol <span class="hlt">concentration</span> in fish.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Takase, Mai; Murata, Masataka; Hibi, Kyoko; Huifeng, Ren; Endo, Hideaki</p> <p>2014-04-01</p> <p>We developed a wireless monitoring system to monitor fish condition by tracking the change in whole cholesterol <span class="hlt">concentration</span>. The whole cholesterol <span class="hlt">concentration</span> of fish is a source of steroid hormones or indicator of immunity level, which makes its detection important for tracking physiological condition of fish. Wireless monitoring system comprises of mediator-type biosensor and wireless transmission device. Biosensor is implantable to fish body, and transmission device is so light, in that fish is allowed to swim <span class="hlt">freely</span> during monitoring. Cholesterol esterase and oxidase were fixated on to the detection site of biosensor and used to detect the whole cholesterol <span class="hlt">concentration</span>. However, cholesterol oxidase incorporates oxidation-reduction reaction of oxygen for detection, which <span class="hlt">concentration</span> fluctuates easily due to change in environmental condition. Meanwhile, mediator-type biosensor enables monitoring of whole cholesterol <span class="hlt">concentration</span> by using mediator to substitute that oxidation-reduction reaction of oxygen. Characteristic of fabricated mediator-type biosensor was tested. The sensor output current of mediator-type biosensor remained stable compared to output current of non-mediator-type biosensor under fluctuating oxygen <span class="hlt">concentration</span> of 0-8 ppm, which implied that this sensor is less affected by change in <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span>. That biosensor was then implanted into fish for wireless monitoring. As a result, approximately 48 h of real-time monitoring was successful.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5070544','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5070544"><span><span class="hlt">Dissolved</span> organic carbon modulates mercury <span class="hlt">concentrations</span> in insect subsidies from streams to terrestrial consumers</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Chaves-Ulloa, Ramsa; Taylor, Brad W.; Broadley, Hannah J.; Cottingham, Kathryn L.; Baer, Nicholas A.; Weathers, Kathleen C.; Ewing, Holly A.; Chen, Celia Y.</p> <p>2016-01-01</p> <p>Mercury (Hg) <span class="hlt">concentrations</span> in aquatic environments have increased globally, exposing consumers of aquatic organisms to high Hg levels. For both aquatic and terrestrial consumers, exposure to Hg depends on their food sources as well as environmental factors influencing Hg bioavailability. The majority of the research on the transfer of methylmercury (MeHg), a toxic and bioaccumulating form of Hg, between aquatic and terrestrial food webs has focused on terrestrial piscivores. However, a gap exists in our understanding of the factors regulating MeHg bioaccumulation by non-piscivorous terrestrial predators, specifically consumers of adult aquatic insects. Because <span class="hlt">dissolved</span> organic carbon (DOC) binds tightly to MeHg, affecting its transport and availability in aquatic food webs, we hypothesized that DOC affects MeHg transfer from stream food webs to terrestrial predators feeding on emerging adult insects. We tested this hypothesis by collecting data over two years from 10 low-order streams spanning a broad DOC gradient in the Lake Sunapee watershed in New Hampshire. We found that streamwater MeHg <span class="hlt">concentration</span> increased linearly with DOC <span class="hlt">concentration</span>. However, streams with the highest DOC <span class="hlt">concentrations</span> had emerging stream prey and spiders with lower MeHg <span class="hlt">concentrations</span> than streams with intermediate DOC <span class="hlt">concentrations</span>; a pattern that is similar to fish and larval aquatic insects. Furthermore, high MeHg <span class="hlt">concentrations</span> found in spiders show that MeHg transfer in adult aquatic insects is an overlooked but potentially significant pathway of MeHg bioaccumulation in terrestrial food webs. Our results suggest that although MeHg in water increases with DOC, MeHg <span class="hlt">concentrations</span> in stream and terrestrial consumers did not consistently increase with increases in streamwater MeHg <span class="hlt">concentrations</span>. In fact, there was a change from a positive to a negative relationship between aqueous exposure and bioaccumulation at streamwater MeHg <span class="hlt">concentrations</span> associated with DOC above around 5</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27755696','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27755696"><span><span class="hlt">Dissolved</span> organic carbon modulates mercury <span class="hlt">concentrations</span> in insect subsidies from streams to terrestrial consumers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chaves-Ulloa, Ramsa; Taylor, Brad W; Broadley, Hannah J; Cottingham, Kathryn L; Baer, Nicholas A; Weathers, Kathleen C; Ewing, Holly A; Chen, Celia Y</p> <p>2016-09-01</p> <p>Mercury (Hg) <span class="hlt">concentrations</span> in aquatic environments have increased globally, exposing consumers of aquatic organisms to high Hg levels. For both aquatic and terrestrial consumers, exposure to Hg depends on their food sources as well as environmental factors influencing Hg bioavailability. The majority of the research on the transfer of methylmercury (MeHg), a toxic and bioaccumulating form of Hg, between aquatic and terrestrial food webs has focused on terrestrial piscivores. However, a gap exists in our understanding of the factors regulating MeHg bioaccumulation by non-piscivorous terrestrial predators, specifically consumers of adult aquatic insects. Because <span class="hlt">dissolved</span> organic carbon (DOC) binds tightly to MeHg, affecting its transport and availability in aquatic food webs, we hypothesized that DOC affects MeHg transfer from stream food webs to terrestrial predators feeding on emerging adult insects. We tested this hypothesis by collecting data over 2 years from 10 low-order streams spanning a broad DOC gradient in the Lake Sunapee watershed in New Hampshire, USA. We found that streamwater MeHg <span class="hlt">concentration</span> increased linearly with DOC <span class="hlt">concentration</span>. However, streams with the highest DOC <span class="hlt">concentrations</span> had emerging stream prey and spiders with lower MeHg <span class="hlt">concentrations</span> than streams with intermediate DOC <span class="hlt">concentrations</span>; a pattern that is similar to fish and larval aquatic insects. Furthermore, high MeHg <span class="hlt">concentrations</span> found in spiders show that MeHg transfer in adult aquatic insects is an overlooked but potentially significant pathway of MeHg bioaccumulation in terrestrial food webs. Our results suggest that although MeHg in water increases with DOC, MeHg <span class="hlt">concentrations</span> in stream and terrestrial consumers did not consistently increase with increases in streamwater MeHg <span class="hlt">concentrations</span>. In fact, there was a change from a positive to a negative relationship between aqueous exposure and bioaccumulation at streamwater MeHg <span class="hlt">concentrations</span> associated with DOC above ~5</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUFM.B13E..05S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUFM.B13E..05S"><span>Influence of domestic pets on soil <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon, nitrogen, and phosphorus under turfgrass in apartment complexes of Central Texas, USA</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Steele, M.; Aitkenhead-Peterson, J. A.</p> <p>2009-12-01</p> <p>High nitrogen (N) and phosphorus (P) watershed loading rates increases the <span class="hlt">concentration</span> and loads present in urban streams and rivers, resulting in eutrophication and degradation of surface water quality. Domestic pet animal feed may represent a significant proportion of nitrogen loading in urban watersheds, and because it is deposited directly on the watershed surface may have a large effect on N loads in urban surface waters (Baker et al. 2001). Animal manure has long been used to increase soil N and phosphorus <span class="hlt">concentrations</span> for the purpose of growing agricultural crops; however, little is known about unintentional urban manuring resulting from a high density of domesticated pets. The purpose of this study is to determine if the presence of domesticated animals in high density urban developments results in increased <span class="hlt">concentrations</span> of soil <span class="hlt">dissolved</span> organic carbon (DOC), N, and P and the potential to contribute to loading of urban streams. Composite soil samples from the 0 to 5 cm and 5 to 10 cm soil depth were collected from apartment complexes in Bryan/College Station (BCS) and San Antonio, Texas during August, 2009. Apartment complexes were randomly located around the city and were chosen based on their rules regarding pet ownership. Four apartment complexes that allowed all domestic pets were compared to four that did not allow any domestic pets on the property. A 10:1 water extraction of field moist soil was conducted immediately after sampling. Soil water extracts were analyzed for DOC, total <span class="hlt">dissolved</span> nitrogen (TDN), nitrate-N, ammonium-N, <span class="hlt">dissolved</span> organic N, and orthophosphate-P. Results indicated significantly increased <span class="hlt">concentrations</span> of DOC and N species at both depths in BCS apartments that allowed pets compared to those that did not; however, opposite trends were found in San Antonio. There is a trend for increased <span class="hlt">concentrations</span> of orthophosphate-P at both locations. Baker, L.A., D. Hope, Y. Xu, et al. 2001. Nitrogen balance for the central Arizona</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25337629','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25337629"><span>Cellular partitioning of nanoparticulate versus <span class="hlt">dissolved</span> metals in marine phytoplankton.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bielmyer-Fraser, Gretchen K; Jarvis, Tayler A; Lenihan, Hunter S; Miller, Robert J</p> <p>2014-11-18</p> <p>Discharges of metal oxide nanoparticles into aquatic environments are increasing with their use in society, thereby increasing exposure risk for aquatic organisms. Separating the impacts of nanoparticle from <span class="hlt">dissolved</span> metal pollution is critical for assessing the environmental risks of the rapidly growing nanomaterial industry, especially in terms of ecosystem effects. Metal oxides negatively affect several species of marine phytoplankton, which are responsible for most marine primary production. Whether such toxicity is generally due to nanoparticles or exposure to <span class="hlt">dissolved</span> metals liberated from particles is uncertain. The type and severity of toxicity depends in part on whether phytoplankton cells take up and accumulate primarily nanoparticles or <span class="hlt">dissolved</span> metal ions. We compared the responses of the marine diatom, Thalassiosira weissflogii, exposed to ZnO, AgO, and CuO nanoparticles with the responses of T. weissflogii cells exposed to the <span class="hlt">dissolved</span> metals ZnCl2, AgNO3, and CuCl2 for 7 d. Cellular metal accumulation, metal distribution, and algal population growth were measured to elucidate differences in exposure to the different forms of metal. <span class="hlt">Concentration</span>-dependent metal accumulation and reduced population growth were observed in T. weissflogii exposed to nanometal oxides, as well as <span class="hlt">dissolved</span> metals. Significant effects on population growth were observed at the lowest <span class="hlt">concentrations</span> tested for all metals, with similar toxicity for both <span class="hlt">dissolved</span> and nanoparticulate metals. Cellular metal distribution, however, markedly differed between T. weissflogii exposed to nanometal oxides versus those exposed to <span class="hlt">dissolved</span> metals. Metal <span class="hlt">concentrations</span> were highest in the algal cell wall when cells were exposed to metal oxide nanoparticles, whereas algae exposed to <span class="hlt">dissolved</span> metals had higher proportions of metal in the organelle and endoplasmic reticulum fractions. These results have implications for marine plankton communities as well as higher trophic levels, since</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70031401','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70031401"><span>Influence of in-stream diel <span class="hlt">concentration</span> cycles of <span class="hlt">dissolved</span> trace metals on acute toxicity to one-year-old cutthroat trout (Oncorhynchus clarki lewisi)</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Nimick, D.A.; Harper, D.D.; Farag, A.M.; Cleasby, T.E.; MacConnell, Elizabeth; Skaar, D.</p> <p>2007-01-01</p> <p>Extrapolating results of laboratory bioassays to streams is difficult, because conditions such as temperature and <span class="hlt">dissolved</span> metal <span class="hlt">concentrations</span> can change substantially on diel time scales. Field bioassays conducted for 96 h in two mining-affected streams compared the survival of hatchery-raised, metal-nai??ve westslope cutthroat trout (Oncorhynchus clarki lewisi) exposed to <span class="hlt">dissolved</span> (0.1-??m filtration) metal <span class="hlt">concentrations</span> that either exhibited the diel variation observed in streams or were controlled at a constant value. Cadmium and Zn <span class="hlt">concentrations</span> in these streams increased each night by as much as 61 and 125%, respectively, and decreased a corresponding amount the next day, whereas Cu did not display a diel <span class="hlt">concentration</span> cycle. In High Ore Creek (40 km south of Helena, MT, USA), survival (33%) after exposure to natural diel-fluctuating Zn <span class="hlt">concentrations</span> (range, 214-634 ??g/L; mean, 428 ??g/L) was significantly (p = 0.008) higher than survival (14%) after exposure to a controlled, constant Zn <span class="hlt">concentration</span> (422 ??g/L). Similarly, in Dry Fork Belt Creek (70 km southeast of Great Falls, MT, USA), survival (75%) after exposure to diel-fluctuating Zn <span class="hlt">concentrations</span> (range, 266-522 ??g/L; mean, 399 ??g/L) was significantly (p = 0.022) higher than survival (50%) in the constant-<span class="hlt">concentration</span> treatment (392 ??g/L). Survival likely was greater in these diel treatments, both because the periods of lower metal <span class="hlt">concentrations</span> provided some relief for the fish and because toxicity during periods of higher metal <span class="hlt">concentrations</span> was lessened by the simultaneous occurrence each night of lower water temperatures, which reduce the rate of metal uptake. Based on the present study, current water-quality criteria appear to be protective for streams with diel <span class="hlt">concentration</span> cycles of Zn (and, perhaps, Cd) for the hydrologie conditions tested. ?? 2007 SETAC.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://sfbaynutrients.sfei.org/books/reports-and-work-products','USGSPUBS'); return false;" href="http://sfbaynutrients.sfei.org/books/reports-and-work-products"><span><span class="hlt">Dissolved</span> oxygen: Chapter 6</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Senn, David; Downing-Kunz, Maureen; Novick, Emily</p> <p>2016-01-01</p> <p><span class="hlt">Dissolved</span> oxygen (DO) <span class="hlt">concentration</span> serves as an important indicator of estuarine habitat condition, because all aquatic macro-organisms require some minimum DO level to survive and prosper. The instantaneous DO <span class="hlt">concentration</span>, measured at a specific location in the water column, results from a balance between multiple processes that add or remove oxygen (Figure 6.1): primary production produces O2; aerobic respiration in the water column and sediments consumes O2; abiotic or microbially-mediated biogeochemical reactions utilize O2 as an oxidant (e.g., oxidation of ammonium, sulfide, and ferrous iron); O2 exchange occurs across the air:water interface in response to under- or oversaturated DO <span class="hlt">concentrations</span> in the water column; and water currents and turbulent mixing transport DO into and out of zones in the water column. If the oxygen loss rate exceeds the oxygen production or input rate, DO <span class="hlt">concentration</span> decreases. When DO losses exceed production or input over a prolonged enough period of time, hypoxia ((<2-3 mg/L) or anoxia can develop. Persistent hypoxia or anoxia causes stress or death in aquatic organism populations, or for organisms that can escape a hypoxic or anoxic area, the loss of habitat. In addition, sulfide, which is toxic to aquatic organisms and causes odor problems, escapes from sediments under low oxygen conditions. Low <span class="hlt">dissolved</span> oxygen is a common aquatic ecosystem response to elevated organic</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017DokES.476.1084P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017DokES.476.1084P"><span>Long-period variability of oxygen <span class="hlt">dissolved</span> in Black Sea waters</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Polonsky, A. B.; Kotolypova, A. A.</p> <p>2017-09-01</p> <p>Using an archival database from the Institute of Natural and Technical Systems, the low-frequency variability of oxygen <span class="hlt">dissolved</span> in the deep-water and northwestern parts of the Black Sea for the period of 1955-2004 is analyzed. The upper mixed layer (UML) is characterized by quasi-periodic variability in the <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in the interdecadal scale. Deeper, a long-term decrease in the oxygen <span class="hlt">concentration</span> is recorded.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20140012680','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20140012680"><span>A Synthesis of Light Absorption Properties of the Arctic Ocean: Application to Semi-analytical Estimates of <span class="hlt">Dissolved</span> Organic Carbon <span class="hlt">Concentrations</span> from Space</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Matsuoka, A.; Babin, M.; Doxaran, D.; Hooker, S. B.; Mitchell, B. G.; Belanger, S.; Bricaud, A.</p> <p>2014-01-01</p> <p>The light absorption coefficients of particulate and <span class="hlt">dissolved</span> materials are the main factors determining the light propagation of the visible part of the spectrum and are, thus, important for developing ocean color algorithms. While these absorption properties have recently been documented by a few studies for the Arctic Ocean [e.g., Matsuoka et al., 2007, 2011; Ben Mustapha et al., 2012], the datasets used in the literature were sparse and individually insufficient to draw a general view of the basin-wide spatial and temporal variations in absorption. To achieve such a task, we built a large absorption database at the pan-Arctic scale by pooling the majority of published datasets and merging new datasets. Our results showed that the total non-water absorption coefficients measured in the Eastern Arctic Ocean (EAO; Siberian side) are significantly higher 74 than in the Western Arctic Ocean (WAO; North American side). This higher absorption is explained 75 by higher <span class="hlt">concentration</span> of colored <span class="hlt">dissolved</span> organic matter (CDOM) in watersheds on the Siberian 76 side, which contains a large amount of <span class="hlt">dissolved</span> organic carbon (DOC) compared to waters off 77 North America. In contrast, the relationship between the phytoplankton absorption (a()) and chlorophyll a (chl a) <span class="hlt">concentration</span> in the EAO was not significantly different from that in the WAO. Because our semi-analytical CDOM absorption algorithm is based on chl a-specific a() values [Matsuoka et al., 2013], this result indirectly suggests that CDOM absorption can be appropriately erived not only for the WAO but also for the EAO using ocean color data. Derived CDOM absorption values were reasonable compared to in situ measurements. By combining this algorithm with empirical DOC versus CDOM relationships, a semi-analytical algorithm for estimating DOC <span class="hlt">concentrations</span> for coastal waters at the Pan-Arctic scale is presented and applied to satellite ocean color data.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2009/5168/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2009/5168/"><span>Specific Conductance and <span class="hlt">Dissolved</span>-Solids Characteristics for the Green River and Muddy Creek, Wyoming, Water Years 1999-2008</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Clark, Melanie L.; Davidson, Seth L.</p> <p>2009-01-01</p> <p>Southwestern Wyoming is an area of diverse scenery, wildlife, and natural resources that is actively undergoing energy development. The U.S. Department of the Interior's Wyoming Landscape Conservation Initiative is a long-term science-based effort to assess and enhance aquatic and terrestrial habitats at a landscape scale, while facilitating responsible energy development through local collaboration and partnerships. Water-quality monitoring has been conducted by the U.S. Geological Survey on the Green River near Green River, Wyoming, and Muddy Creek near Baggs, Wyoming. This monitoring, which is being conducted in cooperation with State and other Federal agencies and as part of the Wyoming Landscape Conservation Initiative, is in response to concerns about potentially increased <span class="hlt">dissolved</span> solids in the Colorado River Basin as a result of energy development. Because of the need to provide real-time <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> for the Green River and Muddy Creek on the World Wide Web, the U.S. Geological Survey developed regression equations to estimate <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> on the basis of continuous specific conductance using relations between measured specific conductance and <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>. Specific conductance and <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> were less varied and generally lower for the Green River than for Muddy Creek. The median <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> for the site on the Green River was 318 milligrams per liter, and the median <span class="hlt">concentration</span> for the site on Muddy Creek was 943 milligrams per liter. <span class="hlt">Dissolved</span>-solids <span class="hlt">concentrations</span> ranged from 187 to 594 milligrams per liter in samples collected from the Green River during water years 1999-2008. <span class="hlt">Dissolved</span>-solids <span class="hlt">concentrations</span> ranged from 293 to 2,485 milligrams per liter in samples collected from Muddy Creek during water years 2006-08. The differences in <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> in samples collected from the Green River compared to samples collected from Muddy</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2014/5012/pdf/sir2014-5012.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2014/5012/pdf/sir2014-5012.pdf"><span><span class="hlt">Dissolved</span>-solids sources, loads, yields, and <span class="hlt">concentrations</span> in streams of the conterminous United States</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Anning, David W.; Flynn, Marilyn E.</p> <p>2014-01-01</p> <p>Results from the trend analysis and from the SPARROW model indicate that, compared to monitoring stations with no trends or decreasing trends, stations with increasing trends are associated with a smaller percentage of the predicted <span class="hlt">dissolved</span>-solids load originating from geologic sources, and a larger percentage originating from urban lands and road deicers. Conversely, compared to stations with increasing trends or no trends, stations with decreasing trends have a larger percentage of the predicted <span class="hlt">dissolved</span>-solids load originating from geologic sources and a smaller percentage originating from urban lands and road deicers. Stations with decreasing trends also have larger percentages of predicted <span class="hlt">dissolved</span>-solids load originating from cultivated lands and pasture lands, compared to stations with increasing trends or no trends.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21820696','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21820696"><span>The role of phytoplankton in the modulation of <span class="hlt">dissolved</span> and oyster cadmium <span class="hlt">concentrations</span> in Deep Bay, British Columbia, Canada.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cassis, David; Lekhi, Priyanka; Pearce, Christopher M; Ebell, Nadene; Orians, Kristin; Maldonado, Maria T</p> <p>2011-09-15</p> <p>We previously identified <span class="hlt">dissolved</span> cadmium (Cd(diss)) as the main source of this metal in cultured Pacific oysters, Crassostrea gigas, in Deep Bay, British Columbia, Canada (Lekhi et al., 2008). Total suspended particulate Cd (Cd(part)) was not found to be a significant source of oyster Cd (Cd(oys)), with Cd(part) >20 μm negatively correlated with Cd(oys) <span class="hlt">concentration</span>. High phytoplankton abundance in spring and summer was hypothesized to reduce Cd(oys) indirectly by drawing down Cd(diss) and increasing oyster growth. In the present study we expanded on these results by examining specifically how the phytoplankton community composition modulates both Cd(diss) and Cd(oys) <span class="hlt">concentrations</span> in Deep Bay. Based on calculations of nutrients and Cd(diss) drawdown, phytoplankton accounted for approximately 90% of the overall summer reduction in Cd(diss) in the bay. Diatoms were the dominant phytoplankton group, being correlated negatively with Cd(oys) and positively with Cd(part). This suggests that diatom growth mediates the transfer of Cd from the <span class="hlt">dissolved</span> to the particulate phase, resulting in lower Cd(oys). Spring blooms and sporadic harmful algal blooms may mediate a large flux of Cd(part) to the sediments. Thus, phytoplankton act as a sink, rather than a source, of Cd to oysters in Deep Bay and have a crucial role in the seasonality of Cd(oys) by reducing the <span class="hlt">concentration</span> of Cd(diss) during the summer. Based on environmental variables, two descriptive models for annual Cd(oys) <span class="hlt">concentrations</span> were developed using multiple linear regression. The first model (R(2)=0.870) was created to explain the maximum variability in Cd(oys) <span class="hlt">concentrations</span> throughout the year, while the second (R(2)=0.806) was based on parameters that could be measured easily under farm conditions. Oyster age heavily affected both models, with the first model being secondarily affected by temperature and the second one being more sensitive to changes in salinity. Copyright © 2011 Elsevier B.V. All</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70033207','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70033207"><span><span class="hlt">Dissolved</span> and labile <span class="hlt">concentrations</span> of Cd, Cu, Pb, and Zn in the South Fork Coeur d'Alene River, Idaho: Comparisons among chemical equilibrium models and implications for biotic ligand models</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Balistrieri, L.S.; Blank, R.G.</p> <p>2008-01-01</p> <p>In order to evaluate thermodynamic speciation calculations inherent in biotic ligand models, the speciation of <span class="hlt">dissolved</span> Cd, Cu, Pb, and Zn in aquatic systems influenced by historical mining activities is examined using equilibrium computer models and the diffusive gradients in thin films (DGT) technique. Several metal/organic-matter complexation models, including WHAM VI, NICA-Donnan, and Stockholm Humic model (SHM), are used in combination with inorganic speciation models to calculate the thermodynamic speciation of <span class="hlt">dissolved</span> metals and <span class="hlt">concentrations</span> of metal associated with biotic ligands (e.g., fish gills). Maximum dynamic metal <span class="hlt">concentrations</span>, determined from total <span class="hlt">dissolved</span> metal <span class="hlt">concentrations</span> and thermodynamic speciation calculations, are compared with labile metal <span class="hlt">concentrations</span> measured by DGT to assess which metal/organic-matter complexation model best describes metal speciation and, thereby, biotic ligand speciation, in the studied systems. Results indicate that the choice of model that defines metal/organic-matter interactions does not affect calculated <span class="hlt">concentrations</span> of Cd and Zn associated with biotic ligands for geochemical conditions in the study area, whereas <span class="hlt">concentrations</span> of Cu and Pb associated with biotic ligands depend on whether the speciation calculations use WHAM VI, NICA-Donnan, or SHM. Agreement between labile metal <span class="hlt">concentrations</span> and dynamic metal <span class="hlt">concentrations</span> occurs when WHAM VI is used to calculate Cu speciation and SHM is used to calculate Pb speciation. Additional work in systems that contain wide ranges in <span class="hlt">concentrations</span> of multiple metals should incorporate analytical speciation methods, such as DGT, to constrain the speciation component of biotic ligand models. ?? 2008 Elsevier Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011APS..MAR.J9005I','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011APS..MAR.J9005I"><span><span class="hlt">Freely</span> Suspended Nematic Films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Iglesias, Wilder; Choi, Jeffrey; Mann, Elizabeth K.; Jakli, Antal</p> <p>2011-03-01</p> <p>Using one of the most commonly studied synthetic molecule, 4-Cyano-4'-pentylbiphenyl (5CB), we were able to pull <span class="hlt">freely</span> suspended membranes of different thicknesses into circular frames of up to 20mm diameter. Films pulled this way were distorted using a speaker, while a laser light was shone onto them for studying the far field reflection and learn about resonant frequency modes and subtract valuable information about the viscoelastic terms that hold the membrane stable. This work was supported by NFS, grant 0907055.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24288993','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24288993"><span>[Effect of the change in sulphate and <span class="hlt">dissolved</span> oxygen mass <span class="hlt">concentration</span> on metal release in old cast iron distribution pipes].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wu, Yong-li; Shi, Bao-you; Sun, Hui-fang; Zhang, Zhi-huan; Gu, Jun-nong; Wang, Dong-sheng</p> <p>2013-09-01</p> <p>To understand the processes of corrosion by-product release and the consequent "red water" problems caused by the variation of water chemical composition in drinking water distribution system, the effect of sulphate and <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span> on total iron release in corroded old iron pipe sections historically transporting groundwater was investigated in laboratory using small-scale pipe section reactors. The release behaviors of some low-level metals, such as Mn, As, Cr, Cu, Zn and Ni, in the process of iron release were also monitored. The results showed that the total iron and Mn release increased significantly with the increase of sulphate <span class="hlt">concentration</span>, and apparent red water occurred when sulphate <span class="hlt">concentration</span> was above 400 mg x L(-1). With the increase of sulfate <span class="hlt">concentration</span>, the effluent <span class="hlt">concentrations</span> of As, Cr, Cu, Zn and Ni also increased obviously, however, the effluent <span class="hlt">concentrations</span> of these metals were lower than the influent <span class="hlt">concentrations</span> under most circumstances, which indicated that adsorption of these metals by pipe corrosion scales occurred. Increasing DO within a certain range could significantly inhibit the iron release.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017lcnm.book..361S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017lcnm.book..361S"><span>Inclusions in <span class="hlt">freely</span> suspended smectic films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stannarius, Ralf; Harth, Kirsten</p> <p></p> <p>Smectic liquid crystal phases have a unique property: Like soap solutions, they can form stable <span class="hlt">freely</span> suspended films. Their aspect ratios can be larger than one million to one. Such films can serve as models for two-dimensional (2D) uids, with or without in-plane anisotropy. Solid or liquid inclusions trapped in these films by capillary forces can move in the film plane and interact with other inclusions, with film thickness gradients or the film boundaries, and even with the local orientation field. We describe preparation techniques to incorporate particles or droplets in thin smectic films, and optical observation methods. Several aspects make inclusions in <span class="hlt">freely</span> suspended films interesting research objects: They provide rich information on capillary forces as well as surface and interfacial tensions, they can serve as platforms for hydrodynamic studies in 2D, and they may help to understand coalescence dynamics at the transition from 2D to 3D...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_10 --> <div id="page_11" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="201"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMOS53A1161Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMOS53A1161Y"><span>Distribution and composition of <span class="hlt">dissolved</span> amino acids in seawater at the Yap Trench</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yan, Y.; Xie, L.; Sun, C.; Yang, G.; Ding, H.</p> <p>2017-12-01</p> <p>The distributions and compositions of total hydrolyzed amino acids ( THAA) , <span class="hlt">dissolved</span> combined amino acids ( DCAA) and <span class="hlt">dissolved</span> free amino acids ( DFAA) were investigated after analyzing seawater samples collected from different depths by CTD and from the sediment-seawater interface by the Jiaolong submersible, at 4 stations located in the Yap Trench in June, 2016. The results showed that the average <span class="hlt">concentration</span> of THAA was (2.44±0.85) μmol /L, while the average <span class="hlt">concentrations</span> of DCAA and DFAA were (1.97±0.82) μmol /L and (0.47±0.34)μmol /L, respectively.The <span class="hlt">concentrations</span> of THAA and DCAA displayed a decreasing trend from surface layer to deep layer. In the vertical distribution, the <span class="hlt">concentrations</span> of THAA varied differently in superficial layer (above 1000 meters). THAA, DFAA and DCAA had a similar <span class="hlt">concentrations</span> below 1000 meter depth. In the study area, major constituents of <span class="hlt">dissolved</span> amino acids were methionine, threonine , histidine, glutamic acid , valine and glycine. At the Yap Trench, neutral <span class="hlt">dissolved</span> amino acids were dominant in total <span class="hlt">dissolved</span> amino acids. The trend of vertical distributions of various types of THAA, DFAA, and DCAA were similar with the total THAA, DFAA, and DCAA. In sediment-seawater interface, the seawater in the northwest of the trench has high <span class="hlt">concentrations</span> of THAA and DCAA, while the <span class="hlt">concentrations</span> of DFAA were similar in the seawater at the sediment-seawater interface.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JGRG..122.2982V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JGRG..122.2982V"><span>Temporal Dynamics in the <span class="hlt">Concentration</span>, Flux, and Optical Properties of Tree-Derived <span class="hlt">Dissolved</span> Organic Matter in an Epiphyte-Laden Oak-Cedar Forest</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Van Stan, John T.; Wagner, Sasha; Guillemette, François; Whitetree, Ansley; Lewis, Julius; Silva, Leticia; Stubbins, Aron</p> <p>2017-11-01</p> <p>Studies on the fate and transport of <span class="hlt">dissolved</span> organic matter (DOM) along the rainfall-to-discharge flow pathway typically begin in streams or soils, neglecting the initial enrichment of rainfall with DOM during contact with plant canopies. However, rain water can gather significant amounts of tree-derived DOM (tree-DOM) when it drains from the canopy, as throughfall, and down the stem, as stemflow. We examined the temporal variability of event-scale tree-DOM <span class="hlt">concentrations</span>, yield, and optical (light absorbance and fluorescence) characteristics from an epiphyte-laden Quercus virginiana-Juniperus virginiana forest on Skidaway Island, Savannah, Georgia (USA). All tree-DOM fluxes were highly enriched in <span class="hlt">dissolved</span> organic carbon (DOC) compared to rainfall, and epiphytes further increased <span class="hlt">concentrations</span>. Stemflow DOC <span class="hlt">concentrations</span> were greater than throughfall across study species, yet larger throughfall water yields produced greater DOC yields versus stemflow. Tree-DOM optical characteristics indicate it is aromatic-rich with fluorescent DOM dominated by humic-like fluorescence, containing 10-20% protein-like (tryptophan-like) fluorescence. Storm size was the only storm condition that strongly correlated with tree-DOM <span class="hlt">concentration</span> and flux; however, throughfall and stemflow optical characteristics varied little across a wide range of storm conditions (from low magnitude events to intense tropical storms). Annual tree-DOM yields from the study forest (0.8-46 g C m-2 yr-1) were similar to other yields from discrete down-gradient fluxes (litter leachates, soil leachates, and stream discharge) along the rainfall-to-discharge flow path.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1690630','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1690630"><span>The relationship between the <span class="hlt">dissolved</span> inorganic carbon <span class="hlt">concentration</span> and growth rate in marine phytoplankton.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Clark, D R; Flynn, K J</p> <p>2000-01-01</p> <p>A range of marine phytoplankton was grown in closed systems in order to investigate the kinetics of <span class="hlt">dissolved</span> inorganic carbon (DIC) use and the influence of the nitrogen source under conditions of constant pH. The kinetics of DIC use could be described by a rectangular hyperbolic curve, yielding estimations of KG(DIC) (the half saturation constant for carbon-specific growth, i.e. C mu) and mu max (the theoretical maximum C mu). All species attained a KG(DIC) within the range of 30-750 microM DIC. For most species, NH4+ use enabled growth with a lower KG(DIC) and/or, for two species, an increase in mu max. At DIC <span class="hlt">concentrations</span> of > 1.6 mM, C mu was > 90% saturated for all species relative to the rate at the natural seawater DIC <span class="hlt">concentration</span> of 2.0 mM. The results suggest that neither the rate nor the extent of primary productivity will be significantly limited by the DIC in the quasi-steady-state conditions associated with oligotrophic oceans. The method needs to be applied in the conditions associated with dynamic coastal (eutrophic) systems for clarification of a potential DIC rate limitation where cells may grow to higher densities and under variable pH and nitrogen supply. PMID:10874743</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018WRR....54.2112R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018WRR....54.2112R"><span>Spatial and Temporal Dynamics of <span class="hlt">Dissolved</span> Oxygen <span class="hlt">Concentrations</span> and Bioactivity in the Hyporheic Zone</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Reeder, W. Jeffery; Quick, Annika M.; Farrell, Tiffany B.; Benner, Shawn G.; Feris, Kevin P.; Tonina, Daniele</p> <p>2018-03-01</p> <p><span class="hlt">Dissolved</span> oxygen (DO) <span class="hlt">concentrations</span> and consumption rates are primary indicators of heterotrophic respiration and redox conditions in the hyporheic zone (HZ). Due to the complexity of hyporheic flow and interactions between hyporheic hydraulics and the biogeochemical processes, a detailed, mechanistic, and predictive understanding of the biogeochemical activity in the HZ has not yet been developed. Previous studies of microbial activity in the HZ have treated the metabolic DO consumption rate constant (KDO) as a temporally fixed and spatially homogeneous property that is determined primarily by the <span class="hlt">concentration</span> of bioavailable carbon. These studies have generally treated bioactivity as temporally steady state, failing to capture the temporal dynamics of a changeable system. We demonstrate that hyporheic hydraulics controls rate constants in a hyporheic system that is relatively abundant in bioavailable carbon, such that KDO is a linear function of the local downwelling flux. We further demonstrate that, for triangular dunes, the downwelling velocities are lognormally distributed, as are the KDO values. By comparing measured and modeled DO profiles, we demonstrate that treating KDO as a function of the downwelling flux yields a significant improvement in the accuracy of predicted DO profiles. Additionally, our results demonstrate the temporal effect of carbon consumption on microbial respiration rates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012EGUGA..14.7229K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012EGUGA..14.7229K"><span>Chemical characteristics of <span class="hlt">dissolved</span> organic matter (DOM) in relation to heavy metal <span class="hlt">concentrations</span> in soil water from boreal peatlands after clear-cut harvesting</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kiikkilä, O.; Nieminen, T.; Starr, M.; Ukonmaanaho, L.</p> <p>2012-04-01</p> <p>Boreal peatlands form an important terrestrial carbon reserve and are a major source of <span class="hlt">dissolved</span> organic matter (DOM) to surface waters, particularly when disturbed through forestry practices such as draining or timber harvesting. Heavy metals show a strong affinity to organic matter and so, along with DOM, heavy metals can be mobilized and transported from the soil to surface waters and sediments where they may become toxic to aquatic organisms and pass up the food chain. The complexation of heavy metals with DOM can be expected to be related and determined by the chemical characteristics of DOM and oxidation/reducing conditions in the peat. We extracted interstitial water from peat samples and determined the <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon (DOC), <span class="hlt">dissolved</span> organic nitrogen (DON) and Al, Cu, Zn and Fe in various fractions of DOM isolated by adsorption properties (XAD-8 fractionation) and molecular-weight (ultrafiltration). The peat samples were taken from 0-30 and 30-50 cm depth in drained peatland catchments two years after whole-tree or stem-only clear-cut harvesting (Scots pine or Norway spruce) had been carried out. The samples from the upper layer had been subject to alternating saturation/aeration conditions while the deeper layer had been continuously under the water table. The fractionation of DOC and DON according to both adsorption properties and molecular-weight fractions clearly differed between the upper and lower peat layers. While the hydrophobic acid fraction contained proportionally more DOC and DON than the hydrophilic acid fraction in the upper peat layer the results were vice versa in the lower peat layer. High-molecular-weight compounds (> 100 kDa) were proportionally more abundant in the upper and low-molecular-weight compounds (< 1 kDa) in the lower peat layer. These differences are assumed to reflect differences in the aerobic/ anaerobic conditions and degree of decomposition between the two layers. The <span class="hlt">concentrations</span> of Zn, Al</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26247749','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26247749"><span>Influence of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on the start-up of the anammox-based process: ELAN®.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Morales, N; Val del Río, A; Vázquez-Padín, J R; Gutiérrez, R; Fernández-González, R; Icaran, P; Rogalla, F; Campos, J L; Méndez, R; Mosquera-Corral, A</p> <p>2015-01-01</p> <p>The anammox-based process ELAN® was started-up in two different sequencing batch reactor (SBR) pilot plant reactors treating municipal anaerobic digester supernatant. The main difference in the operation of both reactors was the <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span> in the bulk liquid. SBR-1 was started at a DO value of 0.4 mg O2/L whereas SBR-2 was started at DO values of 3.0 mg O2/L. Despite both reactors working at a nitrogen removal rate of around 0.6 g N/(L d), in SBR-1, granules represented only a small fraction of the total biomass and reached a diameter of 1.1 mm after 7 months of operation, while in SBR-2 the biomass was mainly composed of granules with an average diameter of 3.2 mm after the same operational period. Oxygen microelectrode profiling revealed that granules from SBR-2 where only fully penetrated by oxygen with DO <span class="hlt">concentrations</span> of 8 mg O2/L while granules from SBR-1 were already oxygen penetrated at DO <span class="hlt">concentrations</span> of 1 mg O2/L. In this way granules from SBR-2 performed better due to the thick layer of ammonia oxidizing bacteria, which accounted for up to 20% of all the microbial populations, which protected the anammox bacteria from non-suitable liquid media conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23701045','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23701045"><span>Growth, metabolic activity, and productivity of immobilized and <span class="hlt">freely</span> suspended CHO cells in perfusion culture.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hilal-Alnaqbi, Ali; Hu, Alan Y C; Zhang, Zhibing; Al-Rubeai, Mohamed</p> <p>2013-01-01</p> <p>Chinese hamster ovary (CHO) cells producing β-galactosidase (β-gal) were successfully cultured on silicone-based porous microcarriers (ImmobaSil FS) in a 1 L stirred-tank perfusion bioreactor. We studied the growth, metabolism, and productivity of free and immobilized cells to understand cellular activity in immobilized conditions. CHO cells attached to ImmobaSil FS significantly better than to other microcarriers. Scanning electron microscope images showed that the CHO cells thoroughly colonized the porous surfaces of the ImmobaSil FS, exhibiting a spherical morphology with microvilli that extended to anchorage cells on the silicone surface. In perfusion culture, the <span class="hlt">concentration</span> of the attached cells reached 8 × 10(8) cells/mL of carrier, whereas those that remained <span class="hlt">freely</span> suspended reached 2 × 10(7) cells/mL medium. The β-gal <span class="hlt">concentration</span> reached more than 5 unit/mL in perfusion culture, more than fivefold that of batch culture. The maximum <span class="hlt">concentration</span> per microcarrier was proportional to the initial cell density. The specific growth rate, the specific β-gal production rate, the percentage of S phase, and the oxygen uptake rate were all relatively lower for immobilized cells than <span class="hlt">freely</span> suspended cells in the same bioreactor, indicating that not only do cells survive and grow to a greater extent in a free suspension state, but they are also metabolically more active than viable cells inside the pores of the microcarriers. © 2013 International Union of Biochemistry and Molecular Biology, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.H11C0886A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.H11C0886A"><span><span class="hlt">Dissolved</span> Solids in Streams of the Conterminous United States</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Anning, D. W.; Flynn, M.</p> <p>2014-12-01</p> <p>Studies have shown that excessive <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> in water can have adverse effects on the environment and on agricultural, municipal, and industrial water users. Such effects motivated the U.S. Geological Survey's National Water-Quality Assessment Program to develop a SPAtially-Referenced Regression on Watershed Attributes (SPARROW) model to improve the understanding of <span class="hlt">dissolved</span> solids in streams of the United States. Using the SPARROW model, annual <span class="hlt">dissolved</span>-solids loads from 2,560 water-quality monitoring stations were statistically related to several spatial datasets serving as surrogates for <span class="hlt">dissolved</span>-solids sources and transport processes. Sources investigated in the model included geologic materials, road de-icers, urban lands, cultivated lands, and pasture lands. Factors affecting transport from these sources to streams in the model included climate, soil, vegetation, terrain, population, irrigation, and artificial-drainage characteristics. The SPARROW model was used to predict long-term mean annual conditions for <span class="hlt">dissolved</span>-solids sources, loads, yields, and <span class="hlt">concentrations</span> in about 66,000 stream reaches and corresponding incremental catchments nationwide. The estimated total amount of <span class="hlt">dissolved</span> solids delivered to the Nation's streams is 272 million metric tons (Mt) annually, of which 194 million Mt (71%) are from geologic sources, 38 million Mt (14%) are from road de-icers, 18 million Mt (7%) are from pasture lands, 14 million Mt (5 %) are from urban lands, and 8 million Mt (3%) are from cultivated lands. The median incremental-catchment yield delivered to local streams is 26 metric tons per year per square kilometer [(Mt/yr)/km2]. Ten percent of the incremental catchments yield less than 4 (Mt/yr)/km2, and 10 percent yield more than 90 (Mt/yr)/km2. In 13% of the reaches, predicted flow-weighted <span class="hlt">concentrations</span> exceed 500 mg/L—the U.S. Environmental Protection Agency secondary non-enforceable drinking-water standard.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013BGD....1017071M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013BGD....1017071M"><span>A synthesis of light absorption properties of the Pan-Arctic Ocean: application to semi-analytical estimates of <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> from space</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Matsuoka, A.; Babin, M.; Doxaran, D.; Hooker, S. B.; Mitchell, B. G.; Bélanger, S.; Bricaud, A.</p> <p>2013-11-01</p> <p>The light absorption coefficients of particulate and <span class="hlt">dissolved</span> materials are the main factors determining the light propagation of the visible part of the spectrum and are, thus, important for developing ocean color algorithms. While these absorption properties have recently been documented by a few studies for the Arctic Ocean (e.g., Matsuoka et al., 2007, 2011; Ben Mustapha et al., 2012), the datasets used in the literature were sparse and individually insufficient to draw a general view of the basin-wide spatial and temporal variations in absorption. To achieve such a task, we built a large absorption database at the pan-Arctic scale by pooling the majority of published datasets and merging new datasets. Our results showed that the total non-water absorption coefficients measured in the Eastern Arctic Ocean (EAO; Siberian side) are significantly higher than in the Western Arctic Ocean (WAO; North American side). This higher absorption is explained by higher <span class="hlt">concentration</span> of colored <span class="hlt">dissolved</span> organic matter (CDOM) in watersheds on the Siberian side, which contains a large amount of <span class="hlt">dissolved</span> organic carbon (DOC) compared to waters off North America. In contrast, the relationship between the phytoplankton absorption (aφ(λ)) and chlorophyll a (chl a) <span class="hlt">concentration</span> in the EAO was not significantly different from that in the WAO. Because our semi-analytical CDOM absorption algorithm is based on chl a-specific aφ(λ) values (Matsuoka et al., 2013), this result indirectly suggests that CDOM absorption can be appropriately derived not only for the WAO but also for the EAO using ocean color data. Derived CDOM absorption values were reasonable compared to in situ measurements. By combining this algorithm with empirical DOC vs. CDOM relationships, a semi-analytical algorithm for estimating DOC <span class="hlt">concentrations</span> for coastal waters at the Pan-Arctic scale is presented and applied to satellite ocean color data.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70060536','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70060536"><span>Using SPMDs for monitoring hydrophobic organic compounds in urban river water in Korea compared with using conventional water grab samples</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kim, Un-Jung; Kim, Hee Young; Alvarez, David A.; Lee, In-Seok; Oh, Jeong-Eun</p> <p>2014-01-01</p> <p>We aimed to verify the effectiveness of semi-permeablemembrane devices (SPMDs) formonitoring hydrophobic organic compounds, such as polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs), that are not easy to detect using conventional grab samples (because of their low <span class="hlt">concentrations</span>), in water.We used SPMDs and grab samples to monitor PCBs and PBDEs upstream and downstream of a sewage treatment plant (STP) in the Suyeong River in Busan, Korea. <span class="hlt">Concentrations</span> in three different phases (<span class="hlt">freely</span> <span class="hlt">dissolved</span>, apparently <span class="hlt">dissolved</span>, and particulate) were measured, to investigate the aquatic fate of PCBs and PBDEs. The <span class="hlt">freely</span> <span class="hlt">dissolved</span> (SPMD) <span class="hlt">concentrations</span> were 2–3 times higher than the apparently <span class="hlt">dissolved</span> and particulate phase (grab sample) <span class="hlt">concentrations</span>. No meaningful relationships were found between the total PCB and PBDE <span class="hlt">concentrations</span> of the grab sample and SPMD sample because of the different partitioning behaviors and detection frequencies of the individual chemicals. However, the summed <span class="hlt">concentrations</span> of specific PCB and PBDE congeners (that were abundant in all samples) in the grab and SPMD samples correlated well (r2 = 0.7451 for PCBs 28 + 52 + 153, r2 = 0.9987 for PBDEs 28 + 47 + 99). The PBDE <span class="hlt">concentrations</span> measured using SPMDs decreased with increasing distance from the STP, but no apparent dilution effect was found in the grab samples. Our results show that SPMDs could be used to support grab sampling for specific chemicals, or to trace chemical sources (such as STPs) to the aquatic environment.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25697696','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25697696"><span>Effect of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on iron efficiency: Removal of three chloroacetic acids.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tang, Shun; Wang, Xiao-mao; Mao, Yu-qin; Zhao, Yu; Yang, Hong-wei; Xie, Yuefeng F</p> <p>2015-04-15</p> <p>The monochloroacetic, dichloroacetic and trichloroacetic acid (MCAA, DCAA and TCAA) removed by metallic iron under controlled <span class="hlt">dissolved</span> oxygen conditions (0, 0.75, 1.52, 2.59, 3.47 or 7.09 mg/L DO) was investigated in well-mixed batch systems. The removal of CAAs increased first and then decreased with increasing DO <span class="hlt">concentration</span>. Compared with anoxic condition, the reduction of MCAA and DCAA was substantially enhanced in the presence of O2, while TCAA reduction was significantly inhibited above 2.59 mg/L. The 1.52 mg/L DO was optimum for the formation of final product, acetic acid. Chlorine mass balances were 69-102%, and carbon mass balances were 92-105%. With sufficient mass transfer from bulk to the particle surface, the degradation of CAAs was limited by their reduction or migration rate within iron particles, which were dependent on the change of reducing agents and corrosion coatings. Under anoxic conditions, the reduction of CAAs was mainly inhibited by the available reducing agents in the conductive layer. Under low oxic conditions, the increasing reducing agents and thin lepidocrocite layer were favorable for CAA dechlorination. Under high oxic conditions, the redundant oxygen competing for reducing agents and significant lepidocrocite growth became the major restricting factors. Various CAA removal mechanisms could be potentially applied to explaining the effect of DO <span class="hlt">concentration</span> on iron efficiency for contaminant reduction in water and wastewater treatment. Copyright © 2015 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011JHyd..397..175O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011JHyd..397..175O"><span>Spatial distribution of <span class="hlt">dissolved</span> constituents in Icelandic river waters</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Oskarsdottir, Sigrídur Magnea; Gislason, Sigurdur Reynir; Snorrason, Arni; Halldorsdottir, Stefanía Gudrún; Gisladottir, Gudrún</p> <p>2011-02-01</p> <p>SummaryIn this study we map the spatial distribution of selected <span class="hlt">dissolved</span> constituents in Icelandic river waters using GIS methods to study and interpret the connection between river chemistry, bedrock, hydrology, vegetation and aquatic ecology. Five parameters were selected: alkalinity, SiO 2, Mo, F and the <span class="hlt">dissolved</span> inorganic nitrogen and <span class="hlt">dissolved</span> inorganic phosphorus mole ratio (DIN/DIP). The highest <span class="hlt">concentrations</span> were found in rivers draining young rocks within the volcanic rift zone and especially those draining active central volcanoes. However, several catchments on the margins of the rift zone also had high values for these parameters, due to geothermal influence or wetlands within their catchment area. The DIN/DIP mole ratio was higher than 16 in rivers draining old rocks, but lowest in rivers within the volcanic rift zone. Thus primary production in the rivers is limited by fixed <span class="hlt">dissolved</span> nitrogen within the rift zone, but <span class="hlt">dissolved</span> phosphorus in the old Tertiary catchments. Nitrogen fixation within the rift zone can be enhanced by high <span class="hlt">dissolved</span> molybdenum <span class="hlt">concentrations</span> in the vicinity of volcanoes. The river catchments in this study were subdivided into several hydrological categories. Importantly, the variation in the hydrology of the catchments cannot alone explain the variation in <span class="hlt">dissolved</span> constituents. The presence or absence of central volcanoes, young reactive rocks, geothermal systems and wetlands is important for the chemistry of the river waters. We used too many categories within several of the river catchments to be able to determine a statistically significant connection between the chemistry of the river waters and the hydrological categories. More data are needed from rivers draining one single hydrological category. The spatial <span class="hlt">dissolved</span> constituent distribution clearly revealed the difference between the two extremes, the young rocks of the volcanic rift zone and the old Tertiary terrain.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://ar.water.usgs.gov/LOCAL_REPORTS/WRIR_02-4116.pdf','USGSPUBS'); return false;" href="http://ar.water.usgs.gov/LOCAL_REPORTS/WRIR_02-4116.pdf"><span>Simulation of hydrodynamics, temperature, and <span class="hlt">dissolved</span> oxygen in Beaver Lake, Arkansas, 1994-1995</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Haggard, Brian; Green, W. Reed</p> <p>2002-01-01</p> <p>The tailwaters of Beaver Lake and other White River reservoirs support a cold-water trout fishery of significant economic yield in northwestern Arkansas. The Arkansas Game and Fish Commission has requested an increase in existing minimum flows through the Beaver Lake dam to increase the amount of fishable waters downstream. Information is needed to assess the impact of additional minimum flows on temperature and <span class="hlt">dissolved</span>-oxygen qualities of reservoir water above the dam and the release water. A two-dimensional, laterally averaged hydrodynamic, thermal and <span class="hlt">dissolved</span>-oxygen model was developed and calibrated for Beaver Lake, Arkansas. The model simulates surface-water elevation, currents, heat transport and <span class="hlt">dissolved</span>-oxygen dynamics. The model was developed to assess the impacts of proposed increases in minimum flows from 1.76 cubic meters per second (the existing minimum flow) to 3.85 cubic meters per second (the additional minimum flow). Simulations included assessing (1) the impact of additional minimum flows on tailwater temperature and <span class="hlt">dissolved</span>-oxygen quality and (2) increasing initial water-surface elevation 0.5 meter and assessing the impact of additional minimum flow on tailwater temperatures and <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span>. The additional minimum flow simulation (without increasing initial pool elevation) appeared to increase the water temperature (<0.9 degrees Celsius) and decrease <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (<2.2 milligrams per liter) in the outflow discharge. Conversely, the additional minimum flow plus initial increase in pool elevation (0.5 meter) simulation appeared to decrease outflow water temperature (0.5 degrees Celsius) and increase <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (<1.2 milligrams per liter) through time. However, results from both minimum flow scenarios for both water temperature and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> were within the boundaries or similar to the error between measured and simulated water column profile values.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1994/4201/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1994/4201/report.pdf"><span>Surface-water-quality assessment of the lower Kansas River basin, Kansas and Nebraska; distribution of trace-element <span class="hlt">concentrations</span> in <span class="hlt">dissolved</span> and suspended phases, streambed sediment, and fish samples, May 1987 through April 1990</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Tanner, D.Q.</p> <p>1995-01-01</p> <p>The distribution of trace elements in <span class="hlt">dissolved</span> and suspended phases, streambed sediment, and fish samples is described for principal streams in the lower Kansas River Basin, Kansas and Nebraska, from May 1987 through April 1990. Large median <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> lithium and strontium in the Kansas River were related to saline ground-water discharge, and large median <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> strontium in Mill Creek near Paxico, Kansas were related to Permian limestone and shale. Large <span class="hlt">concentrations</span> of arsenic, chromium, and lead in water were identified downstream from three reservoirs, which may be attributed to resuspension of bed sediment in turbulent flow near the dams or release of water from near the bottom of the reservoirs. Trace elements in streambed sediments greater than background <span class="hlt">concentrations</span> were identified downstream from the Aurora, Nebraska, wastewater-treatment plant, from industrial or urban areas near Kansas City, Kansas, and from the dam at Perry Lake, Kansas. Median and 90th-percentile <span class="hlt">concentrations</span> of mercury in fish-tissue samples approximately doubled from 1979-86 to 1987-90. However, <span class="hlt">concentrations</span> in samples collected during the latter period were less than the National Academy of Sciences and National Academy of Engineering 1972 criterion of 500 micrograms per kilogram for mercury in fish tissue.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=336600&keyword=Articles&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=336600&keyword=Articles&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Overview of the U.S. EPA/SERDP/ESTCP: Laboratory, Field, and Analytical Procedures for Using Passive Sampling in the Evaluation of Contaminated Sediments: User’s Manual</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Passive sampling can be used for applications at contaminated sediment sites including performing assessments of contaminant bioavailability (i.e., <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentration</span> (Cfree)), conducting remedial investigations and feasibility studies, and assessing the potential for...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=338548&Lab=NHEERL&keyword=Population+AND+ecology&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=338548&Lab=NHEERL&keyword=Population+AND+ecology&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Overview of the U.S. EPA/SERDP/ESTCP: Laboratory, Field, and Analytical Procedures for Using Passive Sampling in the Evaluation of Contaminated Sediments: User’s Manual.</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Passive sampling is used for applications at contaminated sediment sites including performing assessments of contaminant bioavailability (i.e., <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentration</span> (Cfree)), conducting remedial investigations and feasibility studies, and assessing the potential for con...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29242669','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29242669"><span>Crustacean zooplankton release copious amounts of <span class="hlt">dissolved</span> organic matter as taurine in the ocean.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Clifford, Elisabeth L; Hansell, Dennis A; Varela, Marta M; Nieto-Cid, Mar; Herndl, Gerhard J; Sintes, Eva</p> <p>2017-11-01</p> <p>Taurine (Tau), an amino acid-like compound, is present in almost all marine metazoans including crustacean zooplankton. It plays an important physiological role in these organisms and is released into the ambient water throughout their life cycle. However, limited information is available on the release rates by marine organisms, the <span class="hlt">concentrations</span> and turnover of Tau in the ocean. We determined <span class="hlt">dissolved</span> free Tau <span class="hlt">concentrations</span> throughout the water column and its release by abundant crustacean mesozooplankton at two open ocean sites (Gulf of Alaska and North Atlantic). At both locations, the <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> free Tau were in the low nM range (up to 15.7 nM) in epipelagic waters, declining sharply in the mesopelagic to about 0.2 nM and remaining fairly stable throughout the bathypelagic waters. Pacific amphipod-copepod assemblages exhibited lower <span class="hlt">dissolved</span> free Tau release rates per unit biomass (0.8 ± 0.4 μmol g -1 C-biomass h -1 ) than Atlantic copepods (ranging between 1.3 ± 0.4 μmol g -1 C-biomass h -1 and 9.5 ± 2.1 μmol g -1 C-biomass h -1 ), in agreement with the well-documented inverse relationship between biomass-normalized excretion rates and body size. Our results indicate that crustacean zooplankton might contribute significantly to the <span class="hlt">dissolved</span> organic matter flux in marine ecosystems via <span class="hlt">dissolved</span> free Tau release. Based on the release rates and assuming steady state <span class="hlt">dissolved</span> free Tau <span class="hlt">concentrations</span>, turnover times of <span class="hlt">dissolved</span> free Tau range from 0.05 d to 2.3 d in the upper water column and are therefore similar to those of <span class="hlt">dissolved</span> free amino acids. This rapid turnover indicates that <span class="hlt">dissolved</span> free Tau is efficiently consumed in oceanic waters, most likely by heterotrophic bacteria.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.H11A0844M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.H11A0844M"><span>Assessing the Effects of Water Rights Purchases on <span class="hlt">Dissolved</span> Oxygen, Stream Temperatures, and Fish Habitat</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Mouzon, N. R.; Null, S. E.</p> <p>2014-12-01</p> <p>Human impacts from land and water development have degraded water quality and altered the physical, chemical, and biological integrity of Nevada's Walker River. Reduced instream flows and increased nutrient <span class="hlt">concentrations</span> affect native fish populations through warm daily stream temperatures and low nightly <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>. Water rights purchases are being considered to maintain instream flows, improve water quality, and enhance habitat for native fish species, such as Lahontan cutthroat trout. This study uses the River Modeling System (RMSv4), an hourly, physically-based hydrodynamic and water quality model, to estimate streamflows, temperatures, and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> in the Walker River. We simulate thermal and <span class="hlt">dissolved</span> oxygen changes from increased streamflow to prioritize the time periods and locations that water purchases most enhance native trout habitat. Stream temperatures and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> are proxies for trout habitat. Monitoring results indicate stream temperature and <span class="hlt">dissolved</span> oxygen limitations generally exist in the 115 kilometers upstream of Walker Lake (about 37% of the study area) from approximately May through September, and this reach currently acts as a water quality barrier for fish passage.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20681665','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20681665"><span>On the losses of <span class="hlt">dissolved</span> CO(2) during champagne serving.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liger-Belair, Gérard; Bourget, Marielle; Villaume, Sandra; Jeandet, Philippe; Pron, Hervé; Polidori, Guillaume</p> <p>2010-08-11</p> <p>Pouring champagne into a glass is far from being consequenceless with regard to its <span class="hlt">dissolved</span> CO(2) <span class="hlt">concentration</span>. Measurements of losses of <span class="hlt">dissolved</span> CO(2) during champagne serving were done from a bottled Champagne wine initially holding 11.4 +/- 0.1 g L(-1) of <span class="hlt">dissolved</span> CO(2). Measurements were done at three champagne temperatures (i.e., 4, 12, and 18 degrees C) and for two different ways of serving (i.e., a champagne-like and a beer-like way of serving). The beer-like way of serving champagne was found to impact its <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> CO(2) significantly less. Moreover, the higher the champagne temperature is, the higher its loss of <span class="hlt">dissolved</span> CO(2) during the pouring process, which finally constitutes the first analytical proof that low temperatures prolong the drink's chill and helps it to retain its effervescence during the pouring process. The diffusion coefficient of CO(2) molecules in champagne and champagne viscosity (both strongly temperature-dependent) are suspected to be the two main parameters responsible for such differences. Besides, a recently developed dynamic-tracking technique using IR thermography was also used in order to visualize the cloud of gaseous CO(2) which flows down from champagne during the pouring process, thus visually confirming the strong influence of champagne temperature on its loss of <span class="hlt">dissolved</span> CO(2).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19682711','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19682711"><span>Monitoring the <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> of polycyclic aromatic hydrocarbons (PAH) and alkylphenols (AP) around a Norwegian oil platform by holistic passive sampling.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Harman, Christopher; Thomas, Kevin V; Tollefsen, Knut Erik; Meier, Sonnich; Bøyum, Olav; Grung, Merete</p> <p>2009-11-01</p> <p>In order to assess the environmental impact of aquatic discharges from the offshore oil industry, polar organic chemical integrative samplers (POCIS) and semipermeable membrane devices (SPMDs) were deployed around an oil platform and at reference locations in the North Sea. Exposure to polycyclic aromatic hydrocarbons (PAH) and alkylated phenols (AP) was determined from passive sampler accumulations using an empirical uptake model, the dissipation of performance reference compounds and adjusted laboratory derived sampling rates. Exposure was relatively similar within 1-2 km of the discharge point, with levels dominated by short chained C1-C3 AP isomers (19-51 ngL(-1)) and alkylated naphthalenes, phenanthrenes and dibenzothiophenes (NPD, 29-45 ngL(-1)). Exposure stations showed significant differences to reference sites for NPD, but not always for more hydrophobic PAH. These <span class="hlt">concentrations</span> are several orders of magnitude lower than those reported to give both acute and sub-lethal effects, although their long term consequences are unknown.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_11 --> <div id="page_12" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="221"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27614567','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27614567"><span><span class="hlt">Dissolved</span> trace elements in a nitrogen-polluted river near to the Liaodong Bay in Northeast China.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bu, Hongmei; Song, Xianfang; Guo, Fen</p> <p>2017-01-15</p> <p><span class="hlt">Dissolved</span> trace element <span class="hlt">concentrations</span> (Ba, Fe, Mn, Si, Sr, and Zn) were investigated in the Haicheng River near to the Liaodong Bay in Northeast China during 2010. <span class="hlt">Dissolved</span> Ba, Fe, Mn, and Sr showed significant spatial variation, whereas <span class="hlt">dissolved</span> Fe, Mn, and Zn displayed seasonal variations. Conditions such as water temperature, pH, and <span class="hlt">dissolved</span> oxygen were found to have an important impact on redox reactions involving <span class="hlt">dissolved</span> Ba, Fe, and Zn. <span class="hlt">Dissolved</span> Fe and Mn <span class="hlt">concentrations</span> were regulated by adsorption or desorption of Fe/Mn oxyhydroxides and the effects of organic carbon complexation on <span class="hlt">dissolved</span> Ba and Sr were found to be significant. The sources of <span class="hlt">dissolved</span> trace elements were found to be mainly from domestic sewage, industrial waste, agricultural surface runoff, and natural origin, with estimated seasonal and annual river fluxes established as important inputs of <span class="hlt">dissolved</span> trace elements from the Haicheng River into the Liaodong Bay or Bohai Sea. Copyright © 2016 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/863262','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/863262"><span>Method for <span class="hlt">dissolving</span> plutonium oxide with HI and separating plutonium</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Vondra, Benedict L.; Tallent, Othar K.; Mailen, James C.</p> <p>1979-01-01</p> <p>PuO.sub.2 -containing solids, particularly residues from incomplete HNO.sub.3 dissolution of irradiated nuclear fuels, are <span class="hlt">dissolved</span> in aqueous HI. The resulting solution is evaporated to dryness and the solids are <span class="hlt">dissolved</span> in HNO.sub.3 for further chemical reprocessing. Alternatively, the HI solution containing <span class="hlt">dissolved</span> Pu values, can be contacted with a cation exchange resin causing the Pu values to load the resin. The Pu values are selectively eluted from the resin with more <span class="hlt">concentrated</span> HI.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19452129','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19452129"><span>A new minimal-stress <span class="hlt">freely</span>-moving rat model for preclinical studies on intranasal administration of CNS drugs.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stevens, Jasper; Suidgeest, Ernst; van der Graaf, Piet Hein; Danhof, Meindert; de Lange, Elizabeth C M</p> <p>2009-08-01</p> <p>To develop a new minimal-stress model for intranasal administration in <span class="hlt">freely</span> moving rats and to evaluate in this model the brain distribution of acetaminophen following intranasal versus intravenous administration. Male Wistar rats received one intranasal cannula, an intra-cerebral microdialysis probe, and two blood cannulas for drug administration and serial blood sampling respectively. To evaluate this novel model, the following experiments were conducted. 1) Evans Blue was administered to verify the selectivity of intranasal exposure. 2) During a 1 min infusion 10, 20, or 40 microl saline was administered intranasally or 250 microl intravenously. Corticosterone plasma <span class="hlt">concentrations</span> over time were compared as biomarkers for stress. 3) 200 microg of the model drug acetaminophen was given in identical setup and plasma, and brain pharmacokinetics were determined. In 96% of the rats, only the targeted nasal cavity was deeply colored. Corticosterone plasma <span class="hlt">concentrations</span> were not influenced, neither by route nor volume of administration. Pharmacokinetics of acetaminophen were identical after intravenous and intranasal administration, although the Cmax in microdialysates was reached a little earlier following intravenous administration. A new minimal-stress model for intranasal administration in <span class="hlt">freely</span> moving rats has been successfully developed and allows direct comparison with intravenous administration.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B21C1972P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B21C1972P"><span>Implications for carbon processing beneath the Greenland Ice Sheet from <span class="hlt">dissolved</span> CO2 and CH4 <span class="hlt">concentrations</span> of subglacial discharge</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pain, A.; Martin, J.; Martin, E. E.</p> <p>2017-12-01</p> <p>Subglacial carbon processes are of increasing interest as warming induces ice melting and increases fluxes of glacial meltwater into proglacial rivers and the coastal ocean. Meltwater may serve as an atmospheric source or sink of carbon dioxide (CO2) or methane (CH4), depending on the magnitudes of subglacial organic carbon (OC) remineralization, which produces CO2 and CH4, and mineral weathering reactions, which consume CO2 but not CH4. We report wide variability in <span class="hlt">dissolved</span> CO2 and CH4 <span class="hlt">concentrations</span> at the beginning of the melt season (May-June 2017) between three sites draining land-terminating glaciers of the Greenland Ice Sheet. Two sites, located along the Watson River in western Greenland, drain the Isunnguata and Russell Glaciers and contained 1060 and 400 ppm CO2, respectively. In-situ CO2 flux measurements indicated that the Isunnguata was a source of atmospheric CO2, while the Russell was a sink. Both sites had elevated CH4 <span class="hlt">concentrations</span>, at 325 and 25 ppm CH4, respectively, suggesting active anaerobic OC remineralization beneath the ice sheet. <span class="hlt">Dissolved</span> CO2 and CH4 reached atmospheric equilibrium within 2.6 and 8.6 km downstream of Isunnguata and Russell discharge sites, respectively. These changes reflect rapid gas exchange with the atmosphere and/or CO2 consumption via instream mineral weathering. The third site, draining the Kiagtut Sermiat in southern Greenland, had about half atmospheric CO2 <span class="hlt">concentrations</span> (250 ppm), but approximately atmospheric CH4 <span class="hlt">concentrations</span> (2.1 ppm). Downstream CO2 flux measurements indicated ingassing of CO2 over the entire 10-km length of the proglacial river. CO2 undersaturation may be due to more readily weathered lithologies underlying the Kiagtut Sermiat compared to Watson River sites, but low CH4 <span class="hlt">concentrations</span> also suggest limited contributions of CO2 and CH4 from OC remineralization. These results suggest that carbon processing beneath the Greenland Ice Sheet may be more variable than previously recognized</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=237621&keyword=conducting+AND+scientific+AND+research&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=237621&keyword=conducting+AND+scientific+AND+research&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Equilibrium Partitioning Sediment Benchmarks (ESBs) for the Protection of Benthic Organisms: Procedures for the Determination of the <span class="hlt">Freely</span> <span class="hlt">Dissolved</span> Interstitial Water <span class="hlt">Concentrations</span> of Nonionic Organics</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>This document describes procedures to determine the <span class="hlt">concentrations</span> of nonionic organic chemicals in sediment interstitial waters. In previous ESB documents, the general equilibrium partitioning (EqP) approach was chosen for the derivation of sediment benchmarks because it account...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/12432586','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/12432586"><span>The response of virally infected insect cells to <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span>: recombinant protein production and oxidative damage.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Saarinen, Mark A; Murhammer, David W</p> <p>2003-01-05</p> <p>The effects of <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span> on virally infected insect cells were investigated in 3-L bioreactor culture. Specifically, cultures of Spodoptera frugiperda Sf-9 (Sf-9) and Trichoplusia ni BTI-Tn-5B1-4 (Tn-5B1-4) were infected with Autographa californica multiple nucleopolyhedrovirus expressing secreted alkaline phosphatase (SEAP). Following infection at a DO <span class="hlt">concentration</span> of 50% air saturation, the DO <span class="hlt">concentration</span> was adjusted to a final value of either 190%, 50%, or 10% air saturation. Recombinant SEAP production, cell viability, protein carbonyl content, and thiobarbituric acid reactive substances (TBARS) content were monitored. The increases in protein carbonyl and TBARS contents are taken to be indicators of protein oxidation and lipid oxidation, respectively. DO <span class="hlt">concentration</span> was found to have no noticeable effect on SEAP production or cell viability decline in the Sf-9 cell line. In the Tn-5B1-4 cell line, cells displayed an increased peak SEAP production rate for 190% air saturation and displayed an increased rate of viability decline at increased DO <span class="hlt">concentration</span>. Protein carbonyl content showed no significant increase in the Sf-9 cell line by 72 h postinfection (pi) at any DO <span class="hlt">concentration</span> but showed a twofold increase at 10% and 50% DO <span class="hlt">concentration</span> and a threefold increase at 190% DO <span class="hlt">concentration</span> by 72 h pi in Tn-5B1-4 cells. TBARS content was found to increase by approximately 50% in Sf-9 cells and by approximately twofold in Tn-5B1-4 cells by 72 h pi with no clear relationship to DO <span class="hlt">concentration</span>. It is hypothesized that oxygen uptake changes due to the viral infection process may bear a relation to the observed increases in protein and lipid oxidation and that lipid oxidation may play an important role in the death of virally infected insect cells. Copyright 2002 Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24747699','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24747699"><span>Extracellular wire tetrode recording in brain of <span class="hlt">freely</span> walking insects.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Guo, Peiyuan; Pollack, Alan J; Varga, Adrienn G; Martin, Joshua P; Ritzmann, Roy E</p> <p>2014-04-01</p> <p>Increasing interest in the role of brain activity in insect motor control requires that we be able to monitor neural activity while insects perform natural behavior. We previously developed a technique for implanting tetrode wires into the central complex of cockroach brains that allowed us to record activity from multiple neurons simultaneously while a tethered cockroach turned or altered walking speed. While a major advance, tethered preparations provide access to limited behaviors and often lack feedback processes that occur in <span class="hlt">freely</span> moving animals. We now present a modified version of that technique that allows us to record from the central complex of <span class="hlt">freely</span> moving cockroaches as they walk in an arena and deal with barriers by turning, climbing or tunneling. Coupled with high speed video and cluster cutting, we can now relate brain activity to various parameters of the movement of <span class="hlt">freely</span> behaving insects.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70179749','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70179749"><span>High-frequency in situ optical measurements during a storm event: Assessing relationships between <span class="hlt">dissolved</span> organic matter, sediment <span class="hlt">concentrations</span>, and hydrologic processes</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Saraceno, John F.; Pellerin, Brian A.; Downing, Bryan D.; Boss, Emmanuel; Bachand, Philip A. M.; Bergamaschi, Brian A.</p> <p>2009-01-01</p> <p><span class="hlt">Dissolved</span> organic matter (DOM) dynamics during storm events has received considerable attention in forested watersheds, but the extent to which storms impart rapid changes in DOM <span class="hlt">concentration</span> and composition in highly disturbed agricultural watersheds remains poorly understood. In this study, we used identical in situ optical sensors for DOM fluorescence (FDOM) with and without filtration to continuously evaluate surface water DOM dynamics in a 415 km2agricultural watershed over a 4 week period containing a short-duration rainfall event. Peak turbidity preceded peak discharge by 4 h and increased by over 2 orders of magnitude, while the peak filtered FDOM lagged behind peak turbidity by 15 h. FDOM values reported using the filtered in situ fluorometer increased nearly fourfold and were highly correlated with <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentrations</span> (r2 = 0.97), providing a highly resolved proxy for DOC throughout the study period. Discrete optical properties including specific UV absorbance (SUVA254), spectral slope (S290–350), and fluorescence index (FI) were also strongly correlated with in situ FDOM and indicate a shift toward aromatic, high molecular weight DOM from terrestrially derived sources during the storm. The lag of the peak in FDOM behind peak discharge presumably reflects the draining of watershed soils from natural and agricultural landscapes. Field and experimental evidence showed that unfiltered FDOM measurements underestimated filtered FDOM <span class="hlt">concentrations</span> by up to ∼60% at particle <span class="hlt">concentrations</span> typical of many riverine systems during hydrologic events. Together, laboratory and in situ data provide insights into the timing and magnitude of changes in DOM quantity and quality during storm events in an agricultural watershed, and indicate the need for sample filtration in systems with moderate to high suspended sediment loads.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70196234','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70196234"><span>Effects of sulfide <span class="hlt">concentration</span> and <span class="hlt">dissolved</span> organic matter characteristics on the structure of nanocolloidal metacinnabar</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Poulin, Brett; Gerbig, Chase A.; Kim, Christopher S.; Stegemeier, John P.; Ryan, Joseph N.; Aiken, George R.</p> <p>2017-01-01</p> <p>Understanding the speciation of divalent mercury (Hg(II)) in aquatic systems containing <span class="hlt">dissolved</span> organic matter (DOM) and sulfide is necessary to predict the conversion of Hg(II) to bioavailable methylmercury. We used X-ray absorption spectroscopy to characterize the structural order of mercury in Hg(II)–DOM–sulfide systems for a range of sulfide <span class="hlt">concentration</span> (1–100 μM), DOM aromaticity (specific ultraviolet absorbance (SUVA254)), and Hg(II)–DOM and Hg(II)–DOM–sulfide equilibration times (4–142 h). In all systems, Hg(II) was present as structurally disordered nanocolloidal metacinnabar (β-HgS). β-HgS nanocolloids were significantly smaller or less ordered at lower sulfide <span class="hlt">concentration</span>, as indicated by under-coordination of Hg(II) in β-HgS. The size or structural order of β-HgS nanocolloids increased with increasing sulfide abundance and decreased with increasing SUVA254 of the DOM. The Hg(II)–DOM or Hg(II)–DOM–sulfide equilibration times did not significantly influence the extent of structural order in nanocolloidal β-HgS. Geochemical factors that control the structural order of nanocolloidal β-HgS, which are expected to influence nanocolloid surface reactivity and solubility, should be considered in the context of mercury bioavailability.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012JGRG..117.3001S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012JGRG..117.3001S"><span><span class="hlt">Dissolved</span> organic carbon and chromophoric <span class="hlt">dissolved</span> organic matter properties of rivers in the USA</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Spencer, Robert G. M.; Butler, Kenna D.; Aiken, George R.</p> <p>2012-09-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) <span class="hlt">concentration</span> and chromophoric <span class="hlt">dissolved</span> organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a254, a350, a440) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for <span class="hlt">dissolved</span> organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC <span class="hlt">concentration</span> from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70039884','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70039884"><span><span class="hlt">Dissolved</span> organic carbon and chromophoric <span class="hlt">dissolved</span> organic matter properties of rivers in the USA</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Spencer, Robert G.M.; Butler, Kenna D.; Aiken, George R.</p> <p>2012-01-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) <span class="hlt">concentration</span> and chromophoric <span class="hlt">dissolved</span> organic matter (CDOM) parameters were measured over a range of discharge in 30 U.S. rivers, covering a diverse assortment of fluvial ecosystems in terms of watershed size and landscape drained. Relationships between CDOM absorption at a range of wavelengths (a254, a350, a440) and DOC in the 30 watersheds were found to correlate strongly and positively for the majority of U.S. rivers. However, four rivers (Colorado, Colombia, Rio Grande and St. Lawrence) exhibited statistically weak relationships between CDOM absorption and DOC. These four rivers are atypical, as they either drain from the Great Lakes or experience significant impoundment of water within their watersheds, and they exhibited values for <span class="hlt">dissolved</span> organic matter (DOM) parameters indicative of autochthonous or anthropogenic sources or photochemically degraded allochthonous DOM and thus a decoupling between CDOM and DOC. CDOM quality parameters in the 30 rivers were found to be strongly correlated to DOM compositional metrics derived via XAD fractionation, highlighting the potential for examining DOM biochemical quality from CDOM measurements. This study establishes the ability to derive DOC <span class="hlt">concentration</span> from CDOM absorption for the majority of U.S. rivers, describes characteristics of riverine systems where such an approach is not valid, and emphasizes the possibility of examining DOM composition and thus biogeochemical function via CDOM parameters. Therefore, the usefulness of CDOM measurements, both laboratory-based analyses and in situ instrumentation, for improving spatial and temporal resolution of DOC fluxes and DOM dynamics in future studies is considerable in a range of biogeochemical studies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/of/2007/1272/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/of/2007/1272/"><span>Estimation of <span class="hlt">Freely-Dissolved</span> <span class="hlt">Concentrations</span> of Polychlorinated Biphenyls, 2,3,7,8-Substituted Congeners and Homologs of Polychlorinated dibenzo-p-dioxins and Dibenzofurans in Water for Development of Total Maximum Daily Loadings for the Bluestone River Watershed, Virginia and West Virginia</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Gale, Robert W.</p> <p>2007-01-01</p> <p>The Commonwealth of Virginia Department of Environmental Quality, working closely with the State of West Virginia Department of Environmental Protection and the U.S. Environmental Protection Agency is undertaking a polychlorinated biphenyl source assessment study for the Bluestone River watershed. The study area extends from the Bluefield area of Virginia and West Virginia, targets the Bluestone River and tributaries suspected of contributing to polychlorinated biphenyl, polychlorinated dibenzo-p-dioxin and dibenzofuran contamination, and includes sites near confluences of Big Branch, Brush Fork, and Beaver Pond Creek. The objectives of this study were to gather information about the <span class="hlt">concentrations</span>, patterns, and distribution of these contaminants at specific study sites to expand current knowledge about polychlorinated biphenyl impacts and to identify potential new sources of contamination. Semipermeable membrane devices were used to integratively accumulate the <span class="hlt">dissolved</span> fraction of the contaminants at each site. Performance reference compounds were added prior to deployment and used to determine site-specific sampling rates, enabling estimations of time-weighted average water <span class="hlt">concentrations</span> during the deployed period. Minimum estimated <span class="hlt">concentrations</span> of polychlorinated biphenyl congeners in water were about 1 picogram per liter per congener, and total <span class="hlt">concentrations</span> at study sites ranged from 130 to 18,000 picograms per liter. The lowest <span class="hlt">concentration</span> was 130 picograms per liter, about threefold greater than total hypothetical <span class="hlt">concentrations</span> from background levels in field blanks. Polychlorinated biphenyl <span class="hlt">concentrations</span> in water fell into three groups of sites: low (130-350 picogram per liter); medium (640-3,500 picogram per liter; and high (11,000-18,000 picogram per liter). <span class="hlt">Concentrations</span> at the high sites, Beacon Cave and Beaverpond Branch at the Resurgence, were about four- to sixfold higher than <span class="hlt">concentrations</span> estimated for the medium group of sites</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017ChJOL..35..383S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017ChJOL..35..383S"><span>Spatiotemporal variation of <span class="hlt">dissolved</span> carbohydrates and amino acids in Jiaozhou Bay, China</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Shi, Di; Yang, Guipeng; Sun, Yan; Wu, Guanwei</p> <p>2017-03-01</p> <p>Surface seawater samples were collected from Jiaozhou Bay, China, during six cruises (March-May 2010, September-November 2010) to study the distribution of <span class="hlt">dissolved</span> organic matter including <span class="hlt">dissolved</span> organic carbon (DOC), total <span class="hlt">dissolved</span> carbohydrates, namely monosaccharides (MCHO) and polysaccharides (PCHO) and total hydrolysable amino acids. These included <span class="hlt">dissolved</span> free amino acids (DFAA) and combined amino acids (DCAA). The goal was to investigate possible relationships between these <span class="hlt">dissolved</span> organic compounds and environmental parameters. During spring, the <span class="hlt">concentrations</span> of MCHO and PCHO were 9.6 (2.8-22.6) and 11.0 (2.9-42.5) μmol C/L, respectively. In autumn, MCHO and PCHO were 9.1 (2.6-27.0) and 10.8 (2.4-25.6) μmol C/L, respectively. The spring <span class="hlt">concentrations</span> of DFAA and DCAA were 1.7 (1.1-4.1) and 7.6 (1.1-31.0) μmol C/L, respectively, while in autumn, DFAA and DCAA were 2.3 (1.1-8.0) and 3.3 (0.6-7.2) μmol C/L, respectively. Among these compounds, the <span class="hlt">concentrations</span> of PCHO were the highest, accounting for nearly a quarter of the DOC, followed by MCHO, DCAA and DFAA. The <span class="hlt">concentrations</span> of the organic compounds exhibited a decreasing trend from the coastal to the central regions of the bay. A negative correlation between <span class="hlt">concentrations</span> of DOC and salinity in each cruise suggested that riverine inputs around the bay have an important impact on the distribution of DOC in the surface water. A significant positive correlation was found between DOC and total bacteria count in spring and autumn, suggesting bacteria play an important role in the marine carbon cycle.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3563834','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3563834"><span>Long-term synchronized electrophysiological and behavioral wireless monitoring of <span class="hlt">freely</span> moving animals</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Grand, Laszlo; Ftomov, Sergiu; Timofeev, Igor</p> <p>2012-01-01</p> <p>Parallel electrophysiological recording and behavioral monitoring of <span class="hlt">freely</span> moving animals is essential for a better understanding of the neural mechanisms underlying behavior. In this paper we describe a novel wireless recording technique, which is capable of synchronously recording in vivo multichannel electrophysiological (LFP, MUA, EOG, EMG) and activity data (accelerometer, video) from <span class="hlt">freely</span> moving cats. The method is based on the integration of commercially available components into a simple monitoring system and is complete with accelerometers and the needed signal processing tools. LFP activities of <span class="hlt">freely</span> moving group-housed cats were recorded from multiple intracortical areas and from the hippocampus. EMG, EOG, accelerometer and video were simultaneously acquired with LFP activities 24-h a day for 3 months. These recordings confirm the possibility of using our wireless method for 24-h long-term monitoring of neurophysiological and behavioral data of <span class="hlt">freely</span> moving experimental animals such as cats, ferrets, rabbits and other large animals. PMID:23099345</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E3SWC..3103006S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E3SWC..3103006S"><span>Numerical Solution of a 3-D Advection-Dispersion Model for <span class="hlt">Dissolved</span> Oxygen Distribution in Facultative Ponds</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sunarsih; Sasongko, Dwi P.; Sutrisno</p> <p>2018-02-01</p> <p>This paper describes a mathematical model for the <span class="hlt">dissolved</span> oxygen distribution in the plane of a facultative pond with a certain depth. The purpose of this paper is to determine the variation of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in facultative ponds. The 3-dimensional advection-diffusion equation is solved using the finite difference method Forward Time Central Space (FTCS). Numerical results show that the aerator greatly affects the occurrence of oxygen <span class="hlt">concentration</span> variations in the facultative pond in the certain depth. The <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen decreases as the depth of the pond increases.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24461699','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24461699"><span>Spatial variability of total <span class="hlt">dissolved</span> copper and copper speciation in the inshore waters of Bermuda.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Oldham, V E; Swenson, M M; Buck, K N</p> <p>2014-02-15</p> <p>Total <span class="hlt">dissolved</span> copper (Cu) and Cu speciation were examined from inshore waters of Bermuda, in October 2009 and July-August 2010, to determine the relationship between total <span class="hlt">dissolved</span> Cu, Cu-binding ligands and bioavailable, free, hydrated Cu(2+) <span class="hlt">concentrations</span>. Speciation was performed using competitive ligand exchange-adsorptive cathodic stripping voltammetry (CLE-ACSV). Mean total <span class="hlt">dissolved</span> Cu <span class="hlt">concentrations</span> ranged from 1.4 nM to 19.2 nM, with lowest <span class="hlt">concentrations</span> at sites further from shore, consistent with previous measurements in the Sargasso Sea, and localized Cu enrichment inshore in enclosed harbors. Ligand <span class="hlt">concentrations</span> exceeded <span class="hlt">dissolved</span> [Cu] at most sites, and [Cu(2+)] were correspondingly low at those sites, typically <10(-13) M. One site, Hamilton Harbour, was found to have [Cu] in excess of ligands, resulting in [Cu(2+)] of 10(-10.7) M, and indicating that Cu may be toxic to phytoplankton here. Copyright © 2013 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016RScI...87l5002Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016RScI...87l5002Z"><span>Photonic crystal fiber modal interferometer with Pd/WO3 coating for real-time monitoring of <span class="hlt">dissolved</span> hydrogen <span class="hlt">concentration</span> in transformer oil</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhang, Ya-nan; Wu, Qilu; Peng, Huijie; Zhao, Yong</p> <p>2016-12-01</p> <p>A highly-sensitive and temperature-robust photonic crystal fiber (PCF) modal interferometer coated with Pd/WO3 film was fabricated and studied, aiming for real-time monitoring of <span class="hlt">dissolved</span> hydrogen <span class="hlt">concentration</span> in transformer oil. The sensor probe was fabricated by splicing two segments of a single mode fiber (SMF) with both ends of the PCF. Since the collapse of air holes in the PCF in the interfaces between SMF and PCF, a SMF-PCF-SMF interferometer structure was formed. The Pd/WO3 film was fabricated by sol-gel method and coated on the surface of the PCF by dip-coating method. When the Pd/WO3 film is exposed to hydrogen, both the length and cladding refractive index of the PCF would be changed, resulting in the resonant wavelength shift of the interferometer. Experimental results showed that the hydrogen measurement sensitivity of the proposed sensor can reach 0.109 pm/(μl/l) in the transformer oil, with the measurement range of 0-10 000 μl/l and response time less than 33 min. Besides, the proposed sensor was temperature-insensitive without any compensation process, easy to fabricate without any tapering, polishing, or etching process, low cost and quickly response without any oil-gas separation device. All these performances satisfy the actual need of real-time monitoring of <span class="hlt">dissolved</span> hydrogen <span class="hlt">concentration</span> in the transformer oil.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28040930','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28040930"><span>Photonic crystal fiber modal interferometer with Pd/WO3 coating for real-time monitoring of <span class="hlt">dissolved</span> hydrogen <span class="hlt">concentration</span> in transformer oil.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhang, Ya-Nan; Wu, Qilu; Peng, Huijie; Zhao, Yong</p> <p>2016-12-01</p> <p>A highly-sensitive and temperature-robust photonic crystal fiber (PCF) modal interferometer coated with Pd/WO 3 film was fabricated and studied, aiming for real-time monitoring of <span class="hlt">dissolved</span> hydrogen <span class="hlt">concentration</span> in transformer oil. The sensor probe was fabricated by splicing two segments of a single mode fiber (SMF) with both ends of the PCF. Since the collapse of air holes in the PCF in the interfaces between SMF and PCF, a SMF-PCF-SMF interferometer structure was formed. The Pd/WO 3 film was fabricated by sol-gel method and coated on the surface of the PCF by dip-coating method. When the Pd/WO 3 film is exposed to hydrogen, both the length and cladding refractive index of the PCF would be changed, resulting in the resonant wavelength shift of the interferometer. Experimental results showed that the hydrogen measurement sensitivity of the proposed sensor can reach 0.109 pm/(μl/l) in the transformer oil, with the measurement range of 0-10 000 μl/l and response time less than 33 min. Besides, the proposed sensor was temperature-insensitive without any compensation process, easy to fabricate without any tapering, polishing, or etching process, low cost and quickly response without any oil-gas separation device. All these performances satisfy the actual need of real-time monitoring of <span class="hlt">dissolved</span> hydrogen <span class="hlt">concentration</span> in the transformer oil.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22776258','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22776258"><span>Effect of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (microaerobic and aerobic) on selective enrichment culture for bioaugmentation of acidic industrial wastewater.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Quan, Ying; Han, Hui; Zheng, Shaokui</p> <p>2012-09-01</p> <p>The successful application of bioaugmentation is largely dependent on the selective enrichment of culture with regards to pH, temperature, salt, or specific toxic organic pollutants. In this study, we investigated the effect of <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentrations</span> (aerobic, >2 mg L(-1); microaerobic, <1 mg L(-1)) on yeast enrichment culture for bioaugmentation of acidic industrial wastewater (pH 3.9-4.7). Clone library analyses revealed that the yeast community shifted in response to different DO levels, and that Candida humilis and Candida pseudolambica were individually dominant in the aerobic and microaerobic enrichment cultures. This would significantly influence the isolation results, and further hinder bioaugmentation due to differences in DO environments during the enrichment and application periods. However, differences in the selective enrichment culture cannot be predicted based on differences in pollutant removal performance. Thus, DO <span class="hlt">concentrations</span> (aerobic/microaerobic) should be considered a secondary selective pressure to achieve successful bioaugmentation. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H51P..05A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H51P..05A"><span>Modeling <span class="hlt">Dissolved</span> Solids in the Rincon Valley, New Mexico Using RiverWare</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Abudu, S.; Ahn, S. R.; Sheng, Z.</p> <p>2017-12-01</p> <p>Simulating transport and storage of <span class="hlt">dissolved</span> solids in surface water and underlying alluvial aquifer is essential to evaluate the impacts of surface water operations, groundwater pumping, and climate variability on the spatial and temporal variability of salinity in the Rio Grande Basin. In this study, we developed a monthly RiverWare water quantity and quality model to simulate the both <span class="hlt">concentration</span> and loads of <span class="hlt">dissolved</span> solids for the Rincon Valley, New Mexico from Caballo Reservoir to Leasburg Dam segment of the Rio Grande. The measured flows, <span class="hlt">concentration</span> and loads of <span class="hlt">dissolved</span> solids in the main stream and drains were used to develop RiveWare model using 1980-1988 data for calibration, and 1989-1995 data for validation. The transport of salt is tracked using discretized salt and post-process approaches. Flow and salt exchange between the surface water and adjacent groundwater objects is computed using "soil moisture salt with supplemental flow" method in the RiverWare. In the groundwater objects, the "layered salt" method is used to simulate <span class="hlt">concentration</span> of the <span class="hlt">dissolved</span> solids in the shallow groundwater storage. In addition, the estimated local inflows under different weather conditions by using a calibrated Soil Water Assessment Tool (SWAT) were fed into the RiverWare to refine the simulation of the flow and <span class="hlt">dissolved</span> solids. The results show the salt <span class="hlt">concentration</span> and loads increased at Leasburg Dam, which indicates the river collects salts from the agricultural return flow and the underlying aquifer. The RiverWare model with the local inflow fed by SWAT delivered the better quantification of temporal and spatial salt exchange patterns between the river and the underlying aquifer. The results from the proposed modeling approach can be used to refine the current mass-balance budgets for <span class="hlt">dissolved</span>-solids transport in the Rio Grande, and provide guidelines for planning and decision-making to control salinity in arid river environment.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_12 --> <div id="page_13" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="241"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70017896','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70017896"><span>Isolation and chemical characterization of <span class="hlt">dissolved</span> and colloidal organic matter</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Aiken, G.; Leenheer, J.</p> <p>1993-01-01</p> <p>Commonly used techniques for the <span class="hlt">concentration</span> and isolation of organic matter from water, such as preparative chromatography, ultrafiltration and reverse osmosis, and the methods used to analyze the organic matter obtained by these methods are reviewed. The development of methods to obtain organic matter that is associated with fractions of the <span class="hlt">dissolved</span> organic carbon other than humic substances, such as organic bases, hydrophilic organic acids and colloidal organic matter are discussed. Methods specifically used to study <span class="hlt">dissolved</span> organic nitrogen and <span class="hlt">dissolved</span> organic phosphorous are also discussed. -from Authors</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003GBioC..17.1008W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003GBioC..17.1008W"><span><span class="hlt">Dissolved</span> inorganic phosphorus, <span class="hlt">dissolved</span> iron, and Trichodesmium in the oligotrophic South China Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wu, Jingfeng; Chung, Shi-Wei; Wen, Liang-Saw; Liu, Kon-Kee; Chen, Yuh-Ling Lee; Chen, Houng-Yung; Karl, David M.</p> <p>2003-03-01</p> <p><span class="hlt">Dissolved</span> inorganic phosphorus (DIP) <span class="hlt">concentrations</span> in the oligotrophic surface waters of the South China Sea decrease from ˜20 nM in March 2000 to ˜5 nM in July 2000, in response to seasonal water column stratification. These minimum DIP <span class="hlt">concentrations</span> are one order of magnitude higher than those in the P-limited, iron-replete stratified surface waters of the western North Atlantic, suggesting that the ecosystem in the South China Sea may be limited by bioavailable nitrogen or some trace nutrient rather than DIP. Nutrient enrichment experiments using either nitrate, phosphate or both indicate that nitrogen limits the net growth of phytoplankton in the South China Sea, at least during March and July 2000. The fixed nitrogen limitation may result from the excess phosphate (N:P<16) transported into the South China Sea from the North Pacific relative to microbial population needs, or from iron control of nitrogen fixation. The iron-limited nitrogen fixation hypothesis is supported by the observation of low population densities of Trichodesmium spp. (<48 × 103 trichomes/m3), the putative N2 fixing cyanobacterium, and with low <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> iron (˜0.2-0.3 nM) in the South China Sea surface water. Our results suggest that nitrogen fixation can be limited by available iron even in regions with a high rate of atmospheric dust deposition such as in the South China Sea.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=64311&Lab=NRMRL&keyword=permanganate&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=64311&Lab=NRMRL&keyword=permanganate&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>FIELD MEASUREMENT OF <span class="hlt">DISSOLVED</span> OXYGEN: A COMPARISON OF METHODS</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>The ability to confidently measure the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen (D.O.) in ground water is a key aspect of remedial selection and assessment. Presented here is a comparison of the commonly practiced methods for determining D.O. <span class="hlt">concentrations</span> in ground water, including c...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=251888&Lab=NCER&keyword=Pre+AND+experimental+AND+design&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=251888&Lab=NCER&keyword=Pre+AND+experimental+AND+design&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>UNDERSTANDING AND MANAGING RISKS POSED BY BRINES CONTAINING <span class="hlt">DISSOLVED</span> CARBON DIOXIDE</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p><p>Geologic disposal of supercritical carbon dioxide in saline aquifers and depleted oil and gas fields will cause large volumes of brine to become saturated with <span class="hlt">dissolved</span> CO<sub>2</sub> at <span class="hlt">concentrations</span> of 50 g/l or more.  As CO<sub>2</sub> <span class="hlt">dissolves</span> in brine, the brine de...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JHyd..559..499H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JHyd..559..499H"><span>Modelling daily <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> using least square support vector machine, multivariate adaptive regression splines and M5 model tree</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Heddam, Salim; Kisi, Ozgur</p> <p>2018-04-01</p> <p>In the present study, three types of artificial intelligence techniques, least square support vector machine (LSSVM), multivariate adaptive regression splines (MARS) and M5 model tree (M5T) are applied for modeling daily <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span> using several water quality variables as inputs. The DO <span class="hlt">concentration</span> and water quality variables data from three stations operated by the United States Geological Survey (USGS) were used for developing the three models. The water quality data selected consisted of daily measured of water temperature (TE, °C), pH (std. unit), specific conductance (SC, μS/cm) and discharge (DI cfs), are used as inputs to the LSSVM, MARS and M5T models. The three models were applied for each station separately and compared to each other. According to the results obtained, it was found that: (i) the DO <span class="hlt">concentration</span> could be successfully estimated using the three models and (ii) the best model among all others differs from one station to another.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/fs/2008/3076/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/fs/2008/3076/"><span><span class="hlt">Dissolved</span> Solids in Basin-Fill Aquifers and Streams in the Southwestern United States - Executive Summary</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Anning, David W.</p> <p>2008-01-01</p> <p>The U.S. Geological Survey (USGS) recently completed a regional study in the Southwestern United States to characterize <span class="hlt">dissolved</span>-solids conditions in major water supplies, including important rivers and aquifers. High <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids can degrade a water supply's suitability for important uses, such as drinking water or crop irrigation. In an effort to ensure the continued availability of clean surface and groundwater, USGS scientists identified areas where there have been both increasing and decreasing trends in <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70019294','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70019294"><span>The effect of using different 0.45 μm filter membranes on '<span class="hlt">dissolved</span>' element <span class="hlt">concentrations</span> in natural waters</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Hall, G.E.M.; Bonham-Carter, G. F.; Horowitz, A.J.; Lum, K.; Lemieux, C.; Quemerais, B.; Garbarino, J.R.</p> <p>1996-01-01</p> <p>The effect of 4 different 0.45 ??m pore size filter membrane systems on the '<span class="hlt">dissolved</span>' <span class="hlt">concentration</span> of 28 elements in 5 natural water samples of varying matrix is reported. In 3 of the 5 waters, consistently higher <span class="hlt">concentrations</span> of most elements (minor and trace) are obtained using Nucleopore 47 mm filter and the cellulose acetate/nitrate 47 mm filter than those measured using the 142 mm cellulose nitrate MFS filter or the Gelman capsule 47 mm filter. These distinct and coherent patterns in elemental behaviour disappear for the other 2 samples, an organic-rich peat water of high suspended load and a mineralised sample high in Si and Ca. Thus the nature and degree of filtration artifacts is matrix-dependent. These trends are evident in both data sets produced by 2 independent laboratories using different instrumentation, techniques and calibrating procedures. The average relative standard deviation in elemental <span class="hlt">concentration</span> across the 4 filter types is in the range 9-21%. The presence of such filtration artifacts must be considered in projects where, for example, seasonal variability of water composition is under examination, data from various sources are being merged or hydrogeochemical surveys are being conducted.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26833936','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26833936"><span>Determination of silicone rubber and low-density polyethylene diffusion and polymer/water partition coefficients for emerging contaminants.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Pintado-Herrera, Marina G; Lara-Martín, Pablo A; González-Mazo, Eduardo; Allan, Ian J</p> <p>2016-09-01</p> <p>There is a growing interest in assessing the <span class="hlt">concentration</span> and distribution of new nonregulated organic compounds (emerging contaminants) in the environment. The measurement of <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> using conventional approaches is challenging because of the low <span class="hlt">concentrations</span> that may be encountered and their temporally variable emissions. Absorption-based passive sampling enables the estimation of <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> of hydrophobic contaminants of emerging concern in water. In the present study, calibration was undertaken for 2 polymers, low-density polyethylene (LDPE) and silicone rubber for 11 fragrances, 5 endocrine-disrupting compounds, 7 ultraviolet (UV) filters, and 8 organophosphate flame retardant compounds. Batch experiments were performed to estimate contaminant diffusion coefficients in the polymers (Dp ), which in general decreased with increasing molecular weight. The values for fragrances, endocrine-disrupting compounds, and UV filters were in ranges similar to those previously reported for polycyclic aromatic hydrocarbons, but were 1 order of magnitude lower for organophosphate flame retardant compounds. Silicone rubber had higher Dp values than LDPE and was therefore selected for further experiments to calculate polymer/water partition coefficients (KPW ). The authors observed a positive correlation between log KPW and log octanol/water partition coefficient values. Field testing of silicone rubber passive samplers was undertaken though exposure in the River Alna (Norway) for an exposure time of 21 d to estimate <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentration</span>. Some fragrances and UV filters were predominant over other emerging and regulated contaminants, at levels up to 1600 ng L(-1) for galaxolide and 448 ng L(-1) for octocrylene. Environ Toxicol Chem 2016;35:2162-2172. © 2016 SETAC. © 2016 SETAC.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25287902','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25287902"><span>Effects of long-term land use change on <span class="hlt">dissolved</span> carbon characteristics in the permafrost streams of northeast China.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Guo, Yuedong; Song, Changchun; Wan, Zhongmei; Tan, Wenwen; Lu, Yongzheng; Qiao, Tianhua</p> <p>2014-11-01</p> <p>Permafrost soils act as large sinks of organic carbon but are highly sensitive to interference such as changes in land use, which can greatly influence <span class="hlt">dissolved</span> carbon loads in streams. This study examines the effects of long-term land reclamation on seasonal <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> carbons in the upper reaches of the Nenjiang River, northeast China. A comparison of streams in natural and agricultural systems shows that the <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentration</span> is much lower in the agricultural stream (AG) than in the two natural streams (WAF, wetland dominated; FR, forest dominated), suggesting that land use change is associated with reduced DOC exporting capacity. Moreover, the fluorescence indexes and the ratio of <span class="hlt">dissolved</span> carbon to nitrogen also differ greatly between the natural and agricultural streams, indicating that the chemical characteristics and the origin of the DOC released from the whole reaches are also altered to some extent. Importantly, the exporting <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> inorganic carbon (DIC) and its proportion of total <span class="hlt">dissolved</span> carbon (TDC) substantially increase following land reclamation, which would largely alter the carbon cycling processes in the downstream fluvial system. Although the strong association between the stream discharge and the DOC <span class="hlt">concentration</span> was unchanged, the reduction in total soil organic carbon following land reclamation led to remarkable decline of the total flux and exporting coefficient of the <span class="hlt">dissolved</span> carbons. The results suggest that <span class="hlt">dissolved</span> carbons in permafrost streams have been greatly affected by changes in land use since the 1970s, and the changes in the <span class="hlt">concentration</span> and chemical characteristics of <span class="hlt">dissolved</span> carbons will last until the alteration in both the traditional agriculture pattern and the persistent reclamation activities.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=338150&Lab=NHEERL&keyword=Agreement&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=338150&Lab=NHEERL&keyword=Agreement&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Cross Validation of Two Partitioning-Based Sampling Approaches in Mesocosms Containing PCB Contaminated Field Sediment, Biota, and Activated Carbon Amendment</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>The Gold Standard for determining <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> (Cfree) of hydrophobic organic compounds in sediment interstitial water would be in situ deployment combined with equilibrium sampling, which is generally difficult to achieve. In the present study, ex situ equilib...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?direntryid=335547','PESTICIDES'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?direntryid=335547"><span>Significance of <span class="hlt">dissolved</span> methane in effluents of anaerobically ...</span></a></p> <p><a target="_blank" href="http://www.epa.gov/pesticides/search.htm">EPA Pesticide Factsheets</a></p> <p></p> <p></p> <p>The need for energy efficient Domestic Wastewater (DWW) treatment is increasing annually with population growth and expanding global energy demand. Anaerobic treatment of low strength DWW produces methane which can be used to as an energy product. Temperature sensitivity, low removal efficiencies (Chemical Oxygen Demand (COD), Suspended Solids (SS), and Nutrients), alkalinity demand, and potential greenhouse gas (GHG) emissions have limited its application to warmer climates. Although well designed anaerobic Membrane Bioreactors (AnMBRs) are able to effectively treat DWW at psychrophilic temperatures (10–30 °C), lower temperatures increase methane solubility leading to increased energy losses in the form of <span class="hlt">dissolved</span> methane in the effluent. Estimates of <span class="hlt">dissolved</span> methane losses are typically based on <span class="hlt">concentrations</span> calculated using Henry's Law but advection limitations can lead to supersaturation of methane between 1.34 and 6.9 times equilibrium <span class="hlt">concentrations</span> and 11–100% of generated methane being lost in the effluent. In well mixed systems such as AnMBRs which use biogas sparging to control membrane fouling, actual <span class="hlt">concentrations</span> approach equilibrium values. Non-porous membranes have been used to recover up to 92.6% of <span class="hlt">dissolved</span> methane and well suited for degassing effluents of Upflow Anaerobic Sludge Blanket (UASB) reactors which have considerable solids and organic contents and can cause pore wetting and clogging in microporous membrane modules. Micro</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015FrEaS...3...63S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015FrEaS...3...63S"><span>Utilizing Colored <span class="hlt">Dissolved</span> Organic Matter to Derive <span class="hlt">Dissolved</span> Black Carbon Export by Arctic Rivers</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stubbins, Aron; Spencer, Robert; Mann, Paul; Holmes, R.; McClelland, James; Niggemann, Jutta; Dittmar, Thorsten</p> <p>2015-10-01</p> <p>Wildfires have produced black carbon (BC) since land plants emerged. Condensed aromatic compounds, a form of BC, have accumulated to become a major component of the soil carbon pool. Condensed aromatics leach from soils into rivers, where they are termed <span class="hlt">dissolved</span> black carbon (DBC). The transport of DBC by rivers to the sea is a major term in the global carbon and BC cycles. To estimate Arctic river DBC export, 25 samples collected from the six largest Arctic rivers (Kolyma, Lena, Mackenzie, Ob’, Yenisey and Yukon) were analyzed for <span class="hlt">dissolved</span> organic carbon (DOC), colored <span class="hlt">dissolved</span> organic matter (CDOM), and DBC. A simple, linear regression between DOC and DBC indicated that DBC accounted for 8.9 ± 0.3% DOC exported by Arctic rivers. To improve upon this estimate, an optical proxy for DBC was developed based upon the linear correlation between DBC <span class="hlt">concentrations</span> and CDOM light absorption coefficients at 254 nm (a254). Relatively easy to measure a254 values were determined for 410 Arctic river samples between 2004 and 2010. Each of these a254 values was converted to a DBC <span class="hlt">concentration</span> based upon the linear correlation, providing an extended record of DBC <span class="hlt">concentration</span>. The extended DBC record was coupled with daily discharge data from the six rivers to estimate riverine DBC loads using the LOADEST modeling program. The six rivers studied cover 53% of the pan-Arctic watershed and exported 1.5 ± 0.1 million tons of DBC per year. Scaling up to the full area of the pan-Arctic watershed, we estimate that Arctic rivers carry 2.8 ± 0.3 million tons of DBC from land to the Arctic Ocean each year. This equates to ~8% of Arctic river DOC export, slightly less than indicated by the simpler DBC vs DOC correlation-based estimate. Riverine discharge is predicted to increase in a warmer Arctic. DBC export was positively correlated with river runoff, suggesting that the export of soil BC to the Arctic Ocean is likely to increase as the Arctic warms.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20667424','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20667424"><span>Effects of <span class="hlt">dissolved</span> oxygen on dye removal by zero-valent iron.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Kai-Sung; Lin, Chiou-Liang; Wei, Ming-Chi; Liang, Hsiu-Hao; Li, Heng-Ching; Chang, Chih-Hua; Fang, Yung-Tai; Chang, Shih-Hsien</p> <p>2010-10-15</p> <p>Effects of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> on dye removal by zero-valent iron (Fe(0)) were investigated. The Vibrio fischeri light inhibition test was employed to evaluate toxicity of decolorized solution. Three dyes, Acid Orange 7 (AO7, monoazo), Reactive Red 120 (RR120, diazo), and Acid Blue 9 (AB9, triphenylmethane), were selected as model dyes. The dye <span class="hlt">concentration</span> and Fe(0) dose used were 100 mg L(-1) and 30 g L(-1), respectively. Under anoxic condition, the order for dye decolorization was AO7>RR120>AB9. An increase in the <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> enhanced decolorization and chemical oxygen demand (COD) removal of the three dyes. An increase in gas flow rates also improved dye and COD removals by Fe(0). At <span class="hlt">dissolved</span> oxygen of 6 mg L(-1), more than 99% of each dye was decolorized within 12 min and high COD removals were obtained (97% for AO7, 87% for RR120, and 93% for AB9). The toxicity of decolorized dye solutions was low (I(5)<40%). An increase in DO <span class="hlt">concentrations</span> obviously reduced the toxicity. When DO above 2 mg L(-1) was applied, low iron ion <span class="hlt">concentration</span> (13.6 mg L(-1)) was obtained in the decolorized AO7 solution. 2010 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19970020583&hterms=Hassan&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAuthor-Name%26N%3D0%26No%3D70%26Ntt%3DHassan','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19970020583&hterms=Hassan&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAuthor-Name%26N%3D0%26No%3D70%26Ntt%3DHassan"><span>Soot Formation in <span class="hlt">Freely</span>-Propagating Laminar Premixed Flames</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Lin, K.-C.; Hassan, M. I.; Faeth, G. M.</p> <p>1997-01-01</p> <p>Soot formation within hydrocarbon-fueled flames is an important unresolved problem of combustion science. Thus, the present study is considering soot formation in <span class="hlt">freely</span>-propagating laminar premixed flames, exploiting the microgravity environment to simplify measurements at the high-pressure conditions of interest for many practical applications. The findings of the investigation are relevant to reducing emissions of soot and continuum radiation from combustion processes, to improving terrestrial and spacecraft fire safety, and to developing methods of computational combustion, among others. Laminar premixed flames are attractive for studying soot formation because they are simple one-dimensional flows that are computationally tractable for detailed numerical simulations. Nevertheless, studying soot-containing burner-stabilized laminar premixed flames is problematical: spatial resolution and residence times are limited at the pressures of interest for practical applications, flame structure is sensitive to minor burner construction details so that experimental reproducibility is not very good, consistent burner behavior over the lengthy test programs needed to measure soot formation properties is hard to achieve, and burners have poor durability. Fortunately, many of these problems are mitigated for soot-containing, <span class="hlt">freely</span>-propagating laminar premixed flames. The present investigation seeks to extend work in this laboratory for various soot processes in flames by observing soot formation in <span class="hlt">freely</span>-propagating laminar premixed flames. Measurements are being made at both Normal Gravity (NG) and MicroGravity (MG), using a short-drop free-fall facility to provide MG conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70015482','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70015482"><span>Preservation of samples for <span class="hlt">dissolved</span> mercury</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Hamlin, S.N.</p> <p>1989-01-01</p> <p>Water samples for <span class="hlt">dissolved</span> mercury requires special treatment because of the high chemical mobility and volatility of this element. Widespread use of mercury and its compounds has provided many avenues for contamination of water. Two laboratory tests were done to determine the relative permeabilities of glass and plastic sample bottles to mercury vapor. Plastic containers were confirmed to be quite permeable to airborne mercury, glass containers were virtually impermeable. Methods of preservation include the use of various combinations of acids, oxidants, and complexing agents. The combination of nitric acid and potassium dichromate successfully preserved mercury in a large variety of <span class="hlt">concentrations</span> and <span class="hlt">dissolved</span> forms. Because this acid-oxidant preservative acts as a sink for airborne mercury and plastic containers are permeable to mercury vapor, glass bottles are preferred for sample collection. To maintain a healthy work environment and minimize the potential for contamination of water samples, mercury and its compounds are isolated from the atmosphere while in storage. Concurrently, a program to monitor environmental levels of mercury vapor in areas of potential contamination is needed to define the extent of mercury contamination and to assess the effectiveness of mercury clean-up procedures.Water samples for <span class="hlt">dissolved</span> mercury require special treatment because of the high chemical mobility and volatility of this element. Widespread use of mercury and its compounds has provided many avenues for contamination of water. Two laboratory tests were done to determine the relative permeabilities of glass and plastic sample bottles to mercury vapor. Plastic containers were confirmed to be quite permeable to airborne mercury, glass containers were virtually impermeable. Methods of preservation include the use of various combinations of acids, oxidants, and complexing agents. The combination of nitric acid and potassium dichromate successfully preserved mercury in a</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008AGUFMOS21C1191B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008AGUFMOS21C1191B"><span>Export of <span class="hlt">Dissolved</span> Lignin from Coastal Wetlands to the Louisiana Shelf</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bianchi, T. S.; Dimarco, S. F.; Smith, R. W.; Schreiner, K. M.</p> <p>2008-12-01</p> <p>Here we report on spatial and temporal changes in the <span class="hlt">concentration</span> and composition of <span class="hlt">dissolved</span> lignin- phenols in surface and bottom waters off the Louisiana coast (USA). Samples were collected at 7 stations on 2 cruises (April, and July, 2008) along a transect that spanned from inside Terrebonne Bay, Louisiana (12 m water depth) to the outer-most station on the inner Louisiana shelf (21 m water depth). The highest average <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> organic carbon (DOC) and <span class="hlt">dissolved</span> lignin, during both cruises, occurred at the interface between Terrebonne Bay and the inner shelf. Average DOC and <span class="hlt">dissolved</span> lignin <span class="hlt">concentrations</span> were significantly higher in April than in July across most stations. Based on hydrologic data, these higher <span class="hlt">concentrations</span> clearly reflect a combined mixing of DOM from plume waters to the west and local marsh inputs. The cinnamyl/vanillyl (C/V) and syringyl/vanillyl (S/V) ratios indicated that the predominant source of lignin was from non-woody angiosperms - likely the dominant species of wetland plants Spartina alterniflora and S. patens (Spartina spp.) that border the entire bay. The high vanillic acid to vanillin (Ad/Al)v ratios for all stations were typical of that found near estuarine boundaries, where biologically- and photochemically-mediated lignin decay processes are important. This preliminary data indicates that wetlands provide another source of <span class="hlt">dissolved</span> organic matter (DOM) to the Louisiana shelf that likely contributes to microbial food resources and hence hypoxia, especially in the context of the instability and extensive erosion of these marshes over the past ca. 50 years. This has important implications for the current management plan to reduce hypoxia in the GOM, particularly in those regions that extend west of the nutrient-rich highly productive near-field zones of Atchafalaya-Mississippi river plumes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70037778','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70037778"><span><span class="hlt">Dissolved</span> oxygen as an indicator of bioavailable <span class="hlt">dissolved</span> organic carbon in groundwater</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Chapelle, Francis H.; Bradley, Paul M.; McMahon, Peter B.; Kaiser, Karl; Benner, Ron</p> <p>2012-01-01</p> <p><span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> oxygen (DO) plotted vs. <span class="hlt">dissolved</span> organic carbon (DOC) in groundwater samples taken from a coastal plain aquifer of South Carolina (SC) showed a statistically significant hyperbolic relationship. In contrast, DO-DOC plots of groundwater samples taken from the eastern San Joaquin Valley of California (CA) showed a random scatter. It was hypothesized that differences in the bioavailability of naturally occurring DOC might contribute to these observations. This hypothesis was examined by comparing nine different biochemical indicators of DOC bioavailability in groundwater sampled from these two systems. <span class="hlt">Concentrations</span> of DOC, total hydrolysable neutral sugars (THNS), total hydrolysable amino acids (THAA), mole% glycine of THAA, initial bacterial cell counts, bacterial growth rates, and carbon dioxide production/consumption were greater in SC samples relative to CA samples. In contrast, the mole% glucose of THNS and the aromaticity (SUVA254) of DOC was greater in CA samples. Each of these indicator parameters were observed to change with depth in the SC system in a manner consistent with active biodegradation. These results are uniformly consistent with the hypothesis that the bioavailability of DOC is greater in SC relative to CA groundwater samples. This, in turn, suggests that the presence/absence of a hyperbolic DO-DOC relationship may be a qualitative indicator of relative DOC bioavailability in groundwater systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21750808','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21750808"><span>Major and trace element partitioning between <span class="hlt">dissolved</span> and particulate phases in Antarctic surface snow.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Grotti, M; Soggia, F; Ardini, F; Magi, E</p> <p>2011-09-01</p> <p>In order to provide a new insight into the Antarctic snow chemistry, partitioning of major and trace elements between <span class="hlt">dissolved</span> and particulate (i.e. insoluble particles, >0.45 μm) phases have been investigated in a number of coastal and inland snow samples, along with their total and acid-<span class="hlt">dissolvable</span> (0.5% nitric acid) <span class="hlt">concentrations</span>. Alkaline and alkaline-earth elements (Na, K, Ca, Mg, Sr) were mainly present in the <span class="hlt">dissolved</span> phase, while Fe and Al were predominantly associated with the particulate matter, without any significant difference between inland and coastal samples. On the other hand, partitioning of trace elements depended on the sampling site position, showing a general decrease of the particulate fraction by moving from the coast to the plateau. Cd, Cu, Pb and Zn were for the most part in the <span class="hlt">dissolved</span> phase, while Cr was mainly associated with the particulate fraction. Co, Mn and V were equally distributed between <span class="hlt">dissolved</span> and particulate phases in the samples collected from the plateau and preferentially associated with the particulate in the coastal samples. The correlation between the elements and the inter-sample variability of their <span class="hlt">concentration</span> significantly decreased for the plateau samples compared to the coastal ones, according to a change in the relative contribution of the metal sources and in good agreement with the estimated marine and crustal enrichment factors. In addition, samples from the plateau were characterised by higher enrichment factors of anthropogenic elements (Cd, Cr, Cu, Pb and Zn), compared to the coastal area. Finally, it was observed that the acid-<span class="hlt">dissolvable</span> metal <span class="hlt">concentrations</span> were generally lower than the total <span class="hlt">concentration</span> values, showing that the acid treatment can <span class="hlt">dissolve</span> only a given fraction of the metal associated with the particulate (<20% for iron and aluminium).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24374620','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24374620"><span>Geochemical behaviour of <span class="hlt">dissolved</span> trace elements in a monsoon-dominated tropical river basin, Southwestern India.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gurumurthy, G P; Balakrishna, K; Tripti, M; Audry, Stéphane; Riotte, Jean; Braun, J J; Udaya Shankar, H N</p> <p>2014-04-01</p> <p>The study presents a 3-year time series data on <span class="hlt">dissolved</span> trace elements and rare earth elements (REEs) in a monsoon-dominated river basin, the Nethravati River in tropical Southwestern India. The river basin lies on the metamorphic transition boundary which separates the Peninsular Gneiss and Southern Granulitic province belonging to Archean and Tertiary-Quaternary period (Western Dharwar Craton). The basin lithology is mainly composed of granite gneiss, charnockite and metasediment. This study highlights the importance of time series data for better estimation of metal fluxes and to understand the geochemical behaviour of metals in a river basin. The <span class="hlt">dissolved</span> trace elements show seasonality in the river water metal <span class="hlt">concentrations</span> forming two distinct groups of metals. First group is composed of heavy metals and minor elements that show higher <span class="hlt">concentrations</span> during dry season and lesser <span class="hlt">concentrations</span> during the monsoon season. Second group is composed of metals belonging to lanthanides and actinides with higher <span class="hlt">concentration</span> in the monsoon and lower <span class="hlt">concentrations</span> during the dry season. Although the metal <span class="hlt">concentration</span> of both the groups appears to be controlled by the discharge, there are important biogeochemical processes affecting their <span class="hlt">concentration</span>. This includes redox reactions (for Fe, Mn, As, Mo, Ba and Ce) and pH-mediated adsorption/desorption reactions (for Ni, Co, Cr, Cu and REEs). The abundance of Fe and Mn oxyhydroxides as a result of redox processes could be driving the geochemical redistribution of metals in the river water. There is a Ce anomaly (Ce/Ce*) at different time periods, both negative and positive, in case of <span class="hlt">dissolved</span> phase, whereas there is positive anomaly in the particulate and bed sediments. The Ce anomaly correlates with the variations in the <span class="hlt">dissolved</span> oxygen indicating the redistribution of Ce between particulate and <span class="hlt">dissolved</span> phase under acidic to neutral pH and lower <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon. Unlike other</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1347840','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1347840"><span>Impact of wetland decline on decreasing <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> along the Mississippi River continuum</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Duan, Shuiwang; He, Yuxiang; Kaushal, Sujay S.</p> <p></p> <p>Prior to discharging to the ocean, large rivers constantly receive inputs of <span class="hlt">dissolved</span> organic carbon (DOC) from tributaries or fringing floodplains and lose DOC via continuous in situ processing along distances that span thousands of kilometers. Current concepts predicting longitudinal changes in DOC mainly focus on in situ processing or exchange with fringing floodplain wetlands, while effects of heterogeneous watershed characteristics are generally ignored. We analyzed results from a 17-year time-series of DOC measurements made at seven sites and three expeditions along the entire Mississippi River main channel with DOC measurements made every 17 km. The results show a clearmore » downstream decrease in DOC <span class="hlt">concentrations</span> that was consistent throughout the entire study period. Downstream DOC decreases were primarily (~63–71%) a result of constant dilutions by low-DOC tributary water controlled by watershed wetland distribution, while in situ processing played a secondary role. We estimate that from 1780 to 1980 wetland loss due to land-use alterations caused a ca. 58% decrease in in DOC <span class="hlt">concentrations</span> in the tributaries of the Mississippi River. DOC reductions caused by watershed wetland loss likely impacted the capacity for the river to effectively remove nitrogen via denitrification, which can further exacerbate coastal hypoxia. Lastly, these findings highlight the importance of watershed wetlands in regulating DOC longitudinally along the headland to ocean continuum of major rivers.« less</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_13 --> <div id="page_14" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="261"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1347840-impact-wetland-decline-decreasing-dissolved-organic-carbon-concentrations-along-mississippi-river-continuum','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1347840-impact-wetland-decline-decreasing-dissolved-organic-carbon-concentrations-along-mississippi-river-continuum"><span>Impact of wetland decline on decreasing <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> along the Mississippi River continuum</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Duan, Shuiwang; He, Yuxiang; Kaushal, Sujay S.; ...</p> <p>2017-01-09</p> <p>Prior to discharging to the ocean, large rivers constantly receive inputs of <span class="hlt">dissolved</span> organic carbon (DOC) from tributaries or fringing floodplains and lose DOC via continuous in situ processing along distances that span thousands of kilometers. Current concepts predicting longitudinal changes in DOC mainly focus on in situ processing or exchange with fringing floodplain wetlands, while effects of heterogeneous watershed characteristics are generally ignored. We analyzed results from a 17-year time-series of DOC measurements made at seven sites and three expeditions along the entire Mississippi River main channel with DOC measurements made every 17 km. The results show a clearmore » downstream decrease in DOC <span class="hlt">concentrations</span> that was consistent throughout the entire study period. Downstream DOC decreases were primarily (~63–71%) a result of constant dilutions by low-DOC tributary water controlled by watershed wetland distribution, while in situ processing played a secondary role. We estimate that from 1780 to 1980 wetland loss due to land-use alterations caused a ca. 58% decrease in in DOC <span class="hlt">concentrations</span> in the tributaries of the Mississippi River. DOC reductions caused by watershed wetland loss likely impacted the capacity for the river to effectively remove nitrogen via denitrification, which can further exacerbate coastal hypoxia. Lastly, these findings highlight the importance of watershed wetlands in regulating DOC longitudinally along the headland to ocean continuum of major rivers.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70032847','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70032847"><span>Influence of groundwater recharge and well characteristics on <span class="hlt">dissolved</span> arsenic <span class="hlt">concentrations</span> in southeastern Michigan groundwater</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Meliker, J.R.; Slotnick, M.J.; Avruskin, G.A.; Haack, S.K.; Nriagu, J.O.</p> <p>2009-01-01</p> <p>Arsenic <span class="hlt">concentrations</span> exceeding 10 ??g/l, the United States maximum contaminant level and the World Health Organization guideline value, are frequently reported in groundwater from bedrock and unconsolidated aquifers of southeastern Michigan. Although arsenic-bearing minerals (including arsenian pyrite and oxide/hydroxide phases) have been identified in Marshall Sandstone bedrock of the Mississippian aquifer system and in tills of the unconsolidated aquifer system, mechanisms responsible for arsenic mobilization and subsequent transport in groundwater are equivocal. Recent evidence has begun to suggest that groundwater recharge and characteristics of well construction may affect arsenic mobilization and transport. Therefore, we investigated the relationship between <span class="hlt">dissolved</span> arsenic <span class="hlt">concentrations</span>, reported groundwater recharge rates, well construction characteristics, and geology in unconsolidated and bedrock aquifers. Results of multiple linear regression analyses indicate that arsenic contamination is more prevalent in bedrock wells that are cased in proximity to the bedrock-unconsolidated interface; no other factors were associated with arsenic contamination in water drawn from bedrock or unconsolidated aquifers. Conditions appropriate for arsenic mobilization may be found along the bedrock-unconsolidated interface, including changes in reduction/oxidation potential and enhanced biogeochemical activity because of differences between geologic strata. These results are valuable for understanding arsenic mobilization and guiding well construction practices in southeastern Michigan, and may also provide insights for other regions faced with groundwater arsenic contamination. ?? Springer-Verlag 2008.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=272839&Lab=NHEERL&keyword=POLYMER&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=272839&Lab=NHEERL&keyword=POLYMER&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Passive Sampling Methods for Contaminated Sediments: Practical Guidance for Selection, Calibration, and Implementation</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>This article provides practical guidance on the use of passive sampling methods(PSMs) that target the <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentration</span> (Cfree) for improved exposure assessment of hydrophobic organic chemicals in sediments. Primary considerations for selecting a PSM for a specific a...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=338263&Lab=NHEERL&keyword=quality+AND+life&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=338263&Lab=NHEERL&keyword=quality+AND+life&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Developing sediment remediation goals at superfund sites based on pore water for the protection of benthic organisms from direct toxicity to non-ionic organic contaminants (presentation)</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Passive sampling is becoming a frequently used measurement technique at Superfund sites with contaminated sediments. Passive sampling measures the <span class="hlt">concentrations</span> of <span class="hlt">freely</span> <span class="hlt">dissolved</span> chemicals (Cfrees) in the sediment pore water. Cfree has been found to be a very practical means f...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=60237&keyword=food+AND+selection+AND+criteria&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=60237&keyword=food+AND+selection+AND+criteria&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>VALIDATION OF AMBIENT WATER QUALITY CRITERIA (AWQC) BIOACCUMULATION METHODOLOGY USING FIELD DATA FROM GREEN BAY AND THE HUDSON RIVER</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>In 1998, EPA published its draft revision to the methodology for deriving ambient water quality criteria to protect human health. Four methods were proposed to determine lipid-normalized bioaccumulation factors based on <span class="hlt">freely-dissolved</span> water <span class="hlt">concentrations</span> (BAFs) for nonpolar or...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013JSAES..44....4L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013JSAES..44....4L"><span>Seasonal variability of total <span class="hlt">dissolved</span> fluxes and origin of major <span class="hlt">dissolved</span> elements within a large tropical river: The Orinoco, Venezuela</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Laraque, Alain; Moquet, Jean-Sébastien; Alkattan, Rana; Steiger, Johannes; Mora, Abrahan; Adèle, Georges; Castellanos, Bartolo; Lagane, Christèle; Lopez, José Luis; Perez, Jesus; Rodriguez, Militza; Rosales, Judith</p> <p>2013-07-01</p> <p>Seasonal variations of total <span class="hlt">dissolved</span> fluxes of the lower Orinoco River were calculated taking into account four complete hydrological cycles during a five-year period (2005-2010). The modern <span class="hlt">concentrations</span> of total <span class="hlt">dissolved</span> solids (TDS) of the Orinoco surface waters were compared with data collected during the second half of the last century published in the literature. This comparison leads to the conclusion that chemical composition did not evolve significantly at least over the last thirty to forty years. Surface waters of the Orinoco at Ciudad Bolivar are between bicarbonated calcic and bicarbonated mixed. In comparison to mean values of <span class="hlt">concentrations</span> of total <span class="hlt">dissolved</span> solids (TDS) of world river surface waters (89.2 mg l-1), the Orinoco River at Ciudad Bolivar presents mainly low mineralized surface waters (2005-10: TDS 30 mg l-1). The TDS fluxes passing at this station in direction to the Atlantic Ocean between 2005 and 2010 were estimated at 30 × 106 t yr-1, i.e. 36 t km-2 yr-1. It was observed that the seasonal variations (dry season vs wet season) of total <span class="hlt">dissolved</span> fluxes (TDS and <span class="hlt">dissolved</span> organic carbon (DOC)) are mainly controlled by discharge variations. Two groups of elements have been defined from dilution curves and molar ratio diagrams. Ca2+, Mg2+, HCO3-, Cl- and Na+ mainly come from the same geographic and lithologic area, the Andes. K+ and SiO2 essentially come from the Llanos and the Guayana Shield. These findings are important for understanding fundamental geochemical processes within the Orinoco River basin, but also as a baseline study in the perspective of the development of numerous mining activities related with aluminum and steel industries; and the plans of the Venezuelan government to construct new fluvial ports on the lower Orinoco for the transport of hydrocarbons.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19741606','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19741606"><span>Fgf8 morphogen gradient forms by a source-sink mechanism with <span class="hlt">freely</span> diffusing molecules.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yu, Shuizi Rachel; Burkhardt, Markus; Nowak, Matthias; Ries, Jonas; Petrásek, Zdenek; Scholpp, Steffen; Schwille, Petra; Brand, Michael</p> <p>2009-09-24</p> <p>It is widely accepted that tissue differentiation and morphogenesis in multicellular organisms are regulated by tightly controlled <span class="hlt">concentration</span> gradients of morphogens. How exactly these gradients are formed, however, remains unclear. Here we show that Fgf8 morphogen gradients in living zebrafish embryos are established and maintained by two essential factors: fast, free diffusion of single molecules away from the source through extracellular space, and a sink function of the receiving cells, regulated by receptor-mediated endocytosis. Evidence is provided by directly examining single molecules of Fgf8 in living tissue by fluorescence correlation spectroscopy, quantifying their local mobility and <span class="hlt">concentration</span> with high precision. By changing the degree of uptake of Fgf8 into its target cells, we are able to alter the shape of the Fgf8 gradient. Our results demonstrate that a <span class="hlt">freely</span> diffusing morphogen can set up <span class="hlt">concentration</span> gradients in a complex multicellular tissue by a simple source-sink mechanism.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/42905-pcbs-pcdd-fs-pahs-dissolved-suspended-settling-particulate-matrixes-from-baltic-sea','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/42905-pcbs-pcdd-fs-pahs-dissolved-suspended-settling-particulate-matrixes-from-baltic-sea"><span>PCBs, PCDD/Fs and PAHs in <span class="hlt">dissolved</span>, suspended and settling particulate matrixes from the Baltic Sea</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Naef, C.; Broman, D.; Zebuehr, Y.</p> <p></p> <p>The occurrence and dynamics of polychlorinated biphenyls (PCBs), dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) and polycyclic aromatic hydrocarbons (PAHs) are discussed on the basis of results from samples taken at pristine coastal and off shore locations in the Baltic Sea. The sampling techniques used were high volume cross flow filtration and sediment traps for suspended and settling particulate matter, respectively, and polyurethane foam adsorbents for the compounds associated with the apparently <span class="hlt">dissolved</span> fractions. All samples were Soxhlet extracted with toluene and separated on a HPLC system followed by quantification on GS/MS. The importance of parameters such as <span class="hlt">concentrations</span> of particulate lipids, particulatemore » organic carbon and <span class="hlt">dissolved</span> organic carbon, etc. for the distribution of the compounds between the suspended and settling particulate matrixes and the <span class="hlt">dissolved</span> phase in the water are discussed. In situ determined particulate organic carbon-water partition coefficients as well as predicted <span class="hlt">dissolved</span> organic carbon-water partition coefficients and approximations of the average ``truly`` <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> are presented. The particulate and <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> in the mixed surface layer are discussed in perspective to the particulate flux of PCBs, PCDD/Fs and PAHs.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4103625','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4103625"><span>Mapping brain function in <span class="hlt">freely</span> moving subjects</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Holschneider, Daniel P.; Maarek, Jean-Michel I.</p> <p>2014-01-01</p> <p>Expression of many fundamental mammalian behaviors such as, for example, aggression, mating, foraging or social behaviors, depend on locomotor activity. A central dilemma in the functional neuroimaging of these behaviors has been the fact that conventional neuroimaging techniques generally rely on immobilization of the subject, which extinguishes all but the simplest activity. Ideally, imaging could occur in <span class="hlt">freely</span> moving subjects, while presenting minimal interference with the subject’s natural behavior. Here we provide an overview of several approaches that have been undertaken in the past to achieve this aim in both tethered and <span class="hlt">freely</span> moving animals, as well as in nonrestrained human subjects. Applications of specific radiotracers to single photon emission computed tomography and positron emission tomography are discussed in which brain activation is imaged after completion of the behavioral task and capture of the tracer. Potential applications to clinical neuropsychiatry are discussed, as well as challenges inherent to constraint-free functional neuroimaging. Future applications of these methods promise to increase our understanding of the neural circuits underlying mammalian behavior in health and disease. PMID:15465134</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.A13G2181S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.A13G2181S"><span>A Global Assessment of Rain-<span class="hlt">Dissolved</span> Organic Carbon</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Safieddine, S.; Heald, C. L.</p> <p>2017-12-01</p> <p>Precipitation is the largest physical removal pathway of atmospheric organic carbon from the atmosphere. The removed carbon is transferred to the land and ocean in the form of <span class="hlt">dissolved</span> organic carbon (DOC). Limited measurements have hindered efforts to characterize global DOC. In this poster presentation, we show the first simulated global DOC distribution based on a GEOS-Chem model simulation of the atmospheric reactive carbon budget. Over the ocean, simulated DOC <span class="hlt">concentrations</span> are between 0.1 to 1 mgCL-1 with a total of 85 TgCyr-1 deposited. DOC <span class="hlt">concentrations</span> are higher inland, ranging between 1 and 10 mgCL-1, producing a total of 188 TgCyr-1 terrestrial organic wet deposition. We compare the 2010 simulated DOC to a 30-year synthesis of available DOC measurements over different environments. Despite imperfect matching of observational and simulated time intervals, the model is able to reproduce much of the spatial variability of DOC (r= 0.63), with a low bias of 35%. We compare the global average carbon oxidation state (OSc) of both atmospheric and <span class="hlt">dissolved</span> organic carbon, as a simple metric for describing the chemical composition of organics. In the global atmosphere reactive organic carbon (ROC) is dominated by hydrocarbons and ketones, and OSc, ranges from -1.8 to -0.6. In the <span class="hlt">dissolved</span> form, formaldehyde, formic acid, primary and secondary semi-volatiles organic aerosol dominate the DOC <span class="hlt">concentrations</span>. The increase in solubility upon oxidation leads to a global increase in OSc in rainwater with -0.6<=OSc <=0. This simulation provides new insight into the current model representation of the flow of atmospheric and rain-<span class="hlt">dissolved</span> organic carbon, and new opportunities to use observations and simulations to understand the DOC reaching land and ocean.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFMOS53C1704L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFMOS53C1704L"><span><span class="hlt">Dissolved</span> and Particulate 230Th - 232Th systematics in the Central Equatorial Pacific Ocean</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lopez, G. I.; Marcantonio, F.</p> <p>2013-12-01</p> <p>To complement our work in the eastern Equatorial Pacific, we have measured total and <span class="hlt">dissolved</span> 230Th and 232Th in the central Equatorial Pacific at two sites, one at 8°N and the other at the equator (ML1208-03CTD; 00° 13.166' S, 155° 57.668' W and ML1208-12CTD; 8° 19.989' N, 159° 18.000' W). The two seawater casts were collected in May 2012 during an NSF-funded "Line Islands" cruise to test for the extent of advection or diffusion of <span class="hlt">dissolved</span> 230Th from the oligotrophic North Pacific gyre (low particle flux) to the more productive equatorial region (high particle flux). Our thorium results are similar to previous data published for the western and central North Pacific Ocean. <span class="hlt">Dissolved</span> 230Th <span class="hlt">concentrations</span> range from 1.1 fg/kg at 100 m to 30.8 fg/kg at 4400 m, while <span class="hlt">dissolved</span> 232Th <span class="hlt">concentrations</span> span from 8.1 pg/kg at 900 m to 19.7 pg/kg at 4400 m. The pattern of the <span class="hlt">dissolved</span> 230Th profile at 8°N is essentially linear from the surface to 2000 m. From 2000 m to 3000 m, the <span class="hlt">dissolved</span> 230Th <span class="hlt">concentrations</span> are constant, and then from 3000 m to the bottom, the profile is linear again. At the same site, the particulate fraction of the total seawater 230Th increases exponentially from about 0% at the surface to 38% at 4400 m. From 0 to 3000 m at 8°N, <span class="hlt">dissolved</span> 232Th <span class="hlt">concentrations</span> display a relatively constant pattern (variability of about 20%). From 3000 m to 4400 m, <span class="hlt">dissolved</span> 232Th contents are more variable, but generally increase toward greater depths. The proportion of 232Th in the particulate fraction of the total seawater sample increases exponentially with depth to a value of 58% in the bottommost sample. We will present additional data from the equator and assess the particulate dynamics that control the distribution of thorium isotopes in central equatorial Pacific seawater.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.B21F0482G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.B21F0482G"><span>Photochemical Reactivity of <span class="hlt">Dissolved</span> Organic Matter in Boreal Lakes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gu, Y.; Vuorio, K.; Tiirola, M.; Perämäki, S.; Vahatalo, A.</p> <p>2016-12-01</p> <p>Boreal lakes are rich in <span class="hlt">dissolved</span> organic matter (DOM) that terrestrially derived from forest soil and wetland, yet little is known about potential for photochemical transformation of aquatic DOM in boreal lakes. Transformation of chromophoric <span class="hlt">dissolved</span> organic matter (CDOM) can decrease water color and enhance microbial mineralization, affecting primary production and respiration, which both affect the CO2 balance of the lakes. We used laboratory solar radiation exposure experiments with lake water samples collected from 54 lakes located in Finland and Sweden, representing different catchment composition and watershed location to assess photochemical reactivity of DOM. The pH of water samples ranged from 5.4 to 8.3, and the <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> iron (Fe) were between < 0.06 and 22 μmol L-1. The filtered water samples received simulated solar radiation corresponding to a daily dose of sunlight, and photomineralization of <span class="hlt">dissolved</span> organic carbon (DOC) to <span class="hlt">dissolved</span> inorganic carbon (DIC) was measured for determination of spectral apparent quantum yields (AQY). During irradiation, photobleaching decreased the absorption coefficients of CDOM at 330 nm between 4.9 and 79 m-1 by 0.5 to 11 m-1. Irradiation generated DIC from 2.8 to 79 μmol C L-1. The AQY at 330 nm ranged between 31 and 273 ×10-6 mol C mol photons-1 h-1, which was correlated positively with <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> Fe, and negatively with pH. Further statistical analyze indicated that the interaction between pH and Fe may explain much of the photochemical reactivity of DOM in the examined lakes, and land cover concerns main catchment areas also can have impact on the photoreaction process. This study may suggest how environmental conditions regulate DOM photomineralization in boreal lakes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2006/5211/PDF/SIR2006_5211.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2006/5211/PDF/SIR2006_5211.pdf"><span>Characterization of <span class="hlt">dissolved</span> solids in water resources of agricultural lands near Manila, Utah, 2004-05</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Gerner, Steven J.; Spangler, L.E.; Kimball, B.A.; Naftz, D.L.</p> <p>2006-01-01</p> <p>Agricultural lands near Manila, Utah, have been identified as contributing <span class="hlt">dissolved</span> solids to Flaming Gorge Reservoir. <span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> solids in water resources of agricultural lands near Manila, Utah, ranged from 35 to 7,410 milligrams per liter. The <span class="hlt">dissolved</span>-solids load in seeps and drains in the study area that discharge to Flaming Gorge Reservoir ranged from less than 0.1 to 113 tons per day. The most substantial source of <span class="hlt">dissolved</span> solids discharging from the study area to the reservoir was Birch Spring Draw. The mean daily <span class="hlt">dissolved</span>-solids load near the mouth of Birch Spring Draw was 65 tons per day.The estimated annual <span class="hlt">dissolved</span>-solids load imported to the study area by Sheep Creek and Peoples Canals is 1,330 and 13,200 tons, respectively. Daily <span class="hlt">dissolved</span>-solid loads discharging to the reservoir from the study area, less the amount of <span class="hlt">dissolved</span> solids imported by canals, for the period July 1, 2004, to June 30, 2005, ranged from 72 to 241 tons per day with a mean of 110 tons per day. The estimated annual <span class="hlt">dissolved</span>-solids load discharging to the reservoir from the study area, less the amount of <span class="hlt">dissolved</span> solids imported by canals, for the same period was 40,200 tons. Of this 40,200 tons of <span class="hlt">dissolved</span> solids, about 9,000 tons may be from a regional source that is not associated with agricultural activities. The salt-loading factor is 3,670 milligrams per liter or about 5.0 tons of <span class="hlt">dissolved</span> solids per acre-foot of deep percolation in Lucerne Valley and 1,620 milligrams per liter or 2.2 tons per acre-foot in South Valley.The variation of δ87Sr with strontium <span class="hlt">concentration</span> indicates some general patterns that help to define a conceptual model of the processes affecting the <span class="hlt">concentration</span> of strontium and the δ87Sr isotopic ratio in area waters. As excess irrigation water percolates through soils derived from Mancos Shale, the δ87Sr isotopic ratio (0.21 to 0.69 permil) approaches one that is typical of deep percolation from irrigation on Mancos</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17363026','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17363026"><span>Stimulating hydrogenotrophic denitrification in simulated groundwater containing high <span class="hlt">dissolved</span> oxygen and nitrate <span class="hlt">concentrations</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Schnobrich, Matthew R; Chaplin, Brian P; Semmens, Michael J; Novak, Paige J</p> <p>2007-05-01</p> <p>In agricultural areas, nitrate (NO3-) is a common groundwater pollutant as a result of extensive fertilizer application. At elevated <span class="hlt">concentrations</span>, NO3- consumption causes methemoglobinemia in infants and has been linked to several cancers; therefore, its removal from groundwater is important. The addition of hydrogen gas (H2) via gas-permeable membranes has been shown to stimulate denitrification in a laboratory-scale reactor. This research, using large columns packed with aquifer material to which a simulated groundwater was fed, was conducted to further identify the conditions required for the use of membrane-delivered H2 in situ. In this study, we show that this novel technology was capable of treating highly contaminated (25 mg/L NO3- -N) and oxygenated (5.5mg/L <span class="hlt">dissolved</span> oxygen) water, but that nutrient addition and gas pressure adjustment was required. Complete NO3- reduction was possible without the accumulation of either NO2- or N2O when the H2 lumen pressure was increased to 17 psi and phosphate was added to the groundwater. The total organic carbon content of the effluent, 110 cm downgradient of H2 addition, did not increase. The results from these experiments demonstrate that this technology can be optimized to provide effective NO3- removal in even challenging field applications.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23110303','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23110303"><span>More on the losses of <span class="hlt">dissolved</span> CO(2) during champagne serving: toward a multiparameter modeling.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liger-Belair, Gérard; Parmentier, Maryline; Cilindre, Clara</p> <p>2012-11-28</p> <p>Pouring champagne into a glass is far from being inconsequential with regard to the <span class="hlt">dissolved</span> CO(2) <span class="hlt">concentration</span> found in champagne. Three distinct bottle types, namely, a magnum bottle, a standard bottle, and a half bottle, were examined with regard to their loss of <span class="hlt">dissolved</span> CO(2) during the service of successively poured flutes. Whatever the bottle size, a decreasing trend is clearly observed with regard to the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> CO(2) found within a flute (from the first to the last one of a whole service). Moreover, when it comes to champagne serving, the bottle size definitely does matter. The higher the bottle volume, the better its buffering capacity with regard to <span class="hlt">dissolved</span> CO(2) found within champagne during the pouring process. Actually, for a given flute number in a pouring data series, the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> CO(2) found within the flute was found to decrease as the bottle size decreases. The impact of champagne temperature (at 4, 12, and 20 °C) on the losses of <span class="hlt">dissolved</span> CO(2) found in successively poured flutes for a given standard 75 cL bottle was also examined. Cold temperatures were found to limit the decreasing trend of <span class="hlt">dissolved</span> CO(2) found within the successively poured flutes (from the first to the last one of a whole service). Our experimental results were discussed on the basis of a multiparameter model that accounts for the major physical parameters that influence the loss of <span class="hlt">dissolved</span> CO(2) during the service of a whole bottle type.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=TESTING+AND+MONOD+AND+%3a+AND+GROWTH+AND+RATE+AND+AS+AND+A+AND+FUNCTION+AND+OF+AND+GLUCOSE+AND+CONCENTRATION+AND+IN+AND+SACCHAROMYCES+AND+CEREVISIAE+AND+Mrwebi%2c+AND+Mandisi+AND+2004-12+AND+Thesis+AND+MSc+AND+--University+AND+Stellenbosch%2c+AND+2004.&pg=5&id=EJ1022658','ERIC'); return false;" href="https://eric.ed.gov/?q=TESTING+AND+MONOD+AND+%3a+AND+GROWTH+AND+RATE+AND+AS+AND+A+AND+FUNCTION+AND+OF+AND+GLUCOSE+AND+CONCENTRATION+AND+IN+AND+SACCHAROMYCES+AND+CEREVISIAE+AND+Mrwebi%2c+AND+Mandisi+AND+2004-12+AND+Thesis+AND+MSc+AND+--University+AND+Stellenbosch%2c+AND+2004.&pg=5&id=EJ1022658"><span>Modeling Fish Growth in Low <span class="hlt">Dissolved</span> Oxygen</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Neilan, Rachael Miller</p> <p>2013-01-01</p> <p>This article describes a computational project designed for undergraduate students as an introduction to mathematical modeling. Students use an ordinary differential equation to describe fish weight and assume the instantaneous growth rate depends on the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen. Published laboratory experiments suggest that continuous…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26988365','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26988365"><span><span class="hlt">Concentration</span>, sources, and flux of <span class="hlt">dissolved</span> organic carbon of precipitation at Lhasa city, the Tibetan Plateau.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Li, Chaoliu; Yan, Fangping; Kang, Shichang; Chen, Pengfei; Qu, Bin; Hu, Zhaofu; Sillanpää, Mika</p> <p>2016-07-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) plays an important role in the climate system, but few data are available on the Tibetan Plateau (TP). In this study, 89 precipitation samples were collected at Lhasa, the largest city of southern Tibet, from March to December 2013. The average <span class="hlt">concentration</span> and wet deposition flux of DOC was 1.10 mg C L(-1) and 0.63 g C m(-2) year(-1), respectively. Seasonally, low DOC <span class="hlt">concentration</span> and high flux appeared during the monsoon period, which were in line with heavy precipitation amount, reflecting dilution effect of precipitation for the DOC. Compared to other regions, the values of Lhasa were lower than those of large cities (e.g., Beijing and Seoul) mainly because of less air pollution of Lhasa. The principal component analysis (PCA) of DOC and ions (Ca(2+), Mg(2+), Na(+), K(+), NH4 (+), Cl(-), NO3 (-), and SO4 (2-)) showed that DOC of Lhasa was derived mainly from the natural sources, followed by anthropogenic burning activities. Furthermore, △(14)C value of DOC indicated that fossil fuel combustion contributed around 28 % of the rainwater DOC of Lhasa, indicating that the atmosphere of Lhasa has been influenced by emission from fossil fuel combustion or high-temperature industrial processes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27295647','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27295647"><span>Cavity Resonator Wireless Power Transfer System for <span class="hlt">Freely</span> Moving Animal Experiments.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mei, Henry; Thackston, Kyle A; Bercich, Rebecca A; Jefferys, John G R; Irazoqui, Pedro P</p> <p>2017-04-01</p> <p>The goal of this paper is to create a large wireless powering arena for powering small devices implanted in <span class="hlt">freely</span> behaving rodents. We design a cavity resonator based wireless power transfer (WPT) system and utilize our previously developed optimal impedance matching methodology to achieve effective WPT performance for operating sophisticated implantable devices, made with miniature receive coils (<8 mm in diameter), within a large volume (dimensions: 60.96 cm × 60.96 cm × 30 cm). We provide unique cavity design and construction methods which maintains electromagnetic performance of the cavity while promoting its utility as a large animal husbandry environment. In addition, we develop a biaxial receive resonator system to address device orientation insensitivity within the cavity environment. Functionality is demonstrated with chronic experiments involving rats implanted with our custom designed bioelectric recording device. We demonstrate an average powering fidelity of 93.53% over nine recording sessions across nine weeks, indicating nearly continuous device operation for a <span class="hlt">freely</span> behaving rat within the large cavity resonator space. We have developed and demonstrated a cavity resonator based WPT system for long term experiments involving <span class="hlt">freely</span> behaving small animals. This cavity resonator based WPT system offers an effective and simple method for wirelessly powering miniaturized devices implanted in <span class="hlt">freely</span> moving small animals within the largest space.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70188892','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70188892"><span>Light climate and <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentration</span> influence species-specific changes in fish zooplanktivory</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Weidel, Brian C.; Baglini, Katherine; Jones, Stuart E.; Kelly, Patrick T.; Solomon, Christopher T.; Zwart, Jacob A.</p> <p>2017-01-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) in lakes reduces light penetration and limits fish production in low nutrient lakes, reportedly via reduced primary and secondary production. Alternatively, DOC and light reductions could influence fish by altering their visual feeding. Previous studies report mixed effects of DOC on feeding rates of zooplanktivorous fish, but most investigators tested effects of a single <span class="hlt">concentration</span> of DOC against clear-water, turbid, or algal treatments. We used a controlled laboratory study to quantify the effects of a DOC gradient (3–19 mg L−1) on average light climate and the zooplankton feeding rate of 3 common, north temperate fishes. Light availability, which was inversely related to DOC <span class="hlt">concentration</span>, had a positive and linear effect on zooplankton consumption by juvenile largemouth bass (Micropterus salmoides) and bluegill (Lepomis macrochirus), explaining 22% and 28% of the variation in consumption, respectively. By contrast, zooplankton feeding rates by fathead minnow (Pimephales promelas) were best predicted by a nonlinear, negative influence of light (R2 = 0.13). In bluegill feeding trials we found a general trend for positive selection of larger zooplankton (Cladocera and Chaoboridae); however, the light climate did not influence the selection of prey type. Largemouth bass selected for larger-bodied zooplankton, with weak evidence that selectivity for large Cladocera changed from negative to neutral selection based on electivity values across the light gradient. Our results suggest that the effect of DOC on the light climate of lakes may directly influence fish zooplanktivory and that this influence may vary among fish species.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008JMS....73..284O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008JMS....73..284O"><span>Diatom stratigraphy and long-term <span class="hlt">dissolved</span> silica <span class="hlt">concentrations</span> in the Baltic Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Olli, Kalle; Clarke, Annemarie; Danielsson, Åsa; Aigars, Juris; Conley, Daniel J.; Tamminen, Timo</p> <p>2008-10-01</p> <p>In many parts of the world coastal waters with anthropogenic eutrophication have experienced a gradual depletion of <span class="hlt">dissolved</span> silica (DSi) stocks. This could put pressure on spring bloom diatom populations, e.g. by limiting the intensity of blooms or by causing shifts in species composition. In addition, eutrophication driven enhanced diatom growth is responsible for the redistribution of DSi from the water phase to the sediments, and changes in the growth conditions may be reflected in the sediment diatom stratigraphy. To test for changes in diatom communities we have analyzed four sediment cores from the Baltic Sea covering approximately the last 100 years. The sediment cores originate from the western Gulf of Finland, the Kattegat, the Baltic Proper and the Gulf of Riga. Three out of the four cores reveal only minor changes in composition of diatom assemblages, while the Gulf of Riga core contains major changes, occurring after the second World War. This area is set apart from the other Baltic Sea basins by a high frequency of low after spring bloom DSi <span class="hlt">concentrations</span> (< 2 µmol L - 1 ) during a relatively well defined time period from 1991-1998. In 1991 to 1993 a rapid decline of DSi spring <span class="hlt">concentrations</span> and winter stocks (down to 5 µmol L - 1 ) in the Gulf was preceded by exceptionally intense diatom spring blooms dominated by the heavily silicified species Thalassiosira baltica (1991-1992; up to 5.5 mg ww L - 1 ). T. baltica has been the principal spring bloom diatom in the Gulf of Riga since records began in 1975. DSi consumption and biomass yield experiments with cultured T. baltica suggest that intense blooms can potentially exhaust the DSi stock of the water column and exceed the annual Si dissolution in the Gulf of Riga. The phytoplankton time series reveals another exceptional T. baltica bloom period in 1981-1983 (up to 8 mg L - 1 ), which, however, took place before the regular DSi measurements. These periods may be reflected in the conspicuous</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_14 --> <div id="page_15" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="281"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43F2184M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43F2184M"><span>The effect of microbial activity and adsorption processes on groundwater <span class="hlt">dissolved</span> organic carbon character and <span class="hlt">concentration</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Meredith, K.; McDonough, L.; Oudone, P.; Rutlidge, H.; O'Carroll, D. M.; Andersen, M. S.; Baker, A.</p> <p>2017-12-01</p> <p>Balancing the terrestrial global carbon budget has proven to be a significant challenge. Whilst the movement of carbon in the atmosphere, rivers and oceans has been extensively studied, the potential for groundwater to act as a carbon source or sink through both microbial activity and sorption to and from mineral surfaces, is poorly understood. To investigate the biodegradable component of groundwater <span class="hlt">dissolved</span> organic carbon (DOC), groundwater samples were collected from multiple coastal and inland sites. Water quality parameters such as pH, electrical conductivity, temperature, <span class="hlt">dissolved</span> oxygen were measured in the field. Samples were analysed and characterised for their biodegradable DOC content using spectrofluorometric and Liquid Chromatography-Organic Carbon Detection (LC-OCD) techniques at set intervals within a 28 day period. Further to this, we performed laboratory sorption experiments on our groundwater samples using different minerals to examine the effect of adsorption processes on DOC character and <span class="hlt">concentration</span>. Calcium carbonate, quartz and iron coated quartz were heated to 400ºC to remove potential carbon contamination, and then added at various known masses (0 mg to 10 g) to 50 mL of groundwater. Samples were then rotated for two hours, filtered at 0.2 μm and analysed by LC-OCD. This research forms part of an ongoing project which will assist in identifying the factors affecting the mobilisation, transport and removal of DOC in uncontaminated groundwater. By quantifying the relative importance of these processes, we can then determine whether the groundwater is a carbon source or sink. Importantly, this information will help guide policy and identify the need to include groundwater resources as part of the carbon economy.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29737247','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29737247"><span><span class="hlt">Freely</span> Accessible Chemical Database Resources of Compounds for in Silico Drug Discovery.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yang, JingFang; Wang, Di; Jia, Chenyang; Wang, Mengyao; Hao, GeFei; Yang, GuangFu</p> <p>2018-05-07</p> <p>In silico drug discovery has been proved to be a solidly established key component in early drug discovery. However, this task is hampered by the limitation of quantity and quality of compound databases for screening. In order to overcome these obstacles, <span class="hlt">freely</span> accessible database resources of compounds have bloomed in recent years. Nevertheless, how to choose appropriate tools to treat these <span class="hlt">freely</span> accessible databases are crucial. To the best of our knowledge, this is the first systematic review on this issue. The existed advantages and drawbacks of chemical databases were analyzed and summarized based on the collected six categories of <span class="hlt">freely</span> accessible chemical databases from literature in this review. Suggestions on how and in which conditions the usage of these databases could be reasonable were provided. Tools and procedures for building 3D structure chemical libraries were also introduced. In this review, we described the <span class="hlt">freely</span> accessible chemical database resources for in silico drug discovery. In particular, the chemical information for building chemical database appears as attractive resources for drug design to alleviate experimental pressure. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.org.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/4151582','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/biblio/4151582"><span>Electrolytic <span class="hlt">dissolver</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Wheelwright, E.J.; Fox, R.D.</p> <p>1975-08-26</p> <p>This patent related to an electrolytic <span class="hlt">dissolver</span> wherein dissolution occurs by solution contact including a vessel of electrically insulative material, a fixed first electrode, a movable second electrode, means for insulating the electrodes from the material to be <span class="hlt">dissolved</span> while permitting a free flow of electrolyte therebetween, means for passing a direct current between the electrodes and means for circulating electrolyte through the <span class="hlt">dissolver</span>. (auth)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.8599C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.8599C"><span>Erosion patterns on <span class="hlt">dissolving</span> blocks</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Courrech du Pont, Sylvain; Cohen, Caroline; Derr, Julien; Berhanu, Michael</p> <p>2016-04-01</p> <p>Patterns in nature are shaped under water flows and wind action, and the understanding of their morphodynamics goes through the identification of the physical mechanisms at play. When a dissoluble body is exposed to a water flow, typical patterns with scallop-like shapes may appear [1,2]. These shapes are observed on the walls of underground rivers or icebergs. We experimentally study the erosion of <span class="hlt">dissolving</span> bodies made of salt, caramel or ice into water solutions without external flow. The <span class="hlt">dissolving</span> mixture, which is created at the solid/liquid interface, undergoes a buoyancy-driven instability comparable to a Rayleigh-Bénard instability so that the <span class="hlt">dissolving</span> front destabilizes into filaments. This mechanism yields to spatial variations of solute <span class="hlt">concentration</span> and to differential dissolution of the <span class="hlt">dissolving</span> block. We first observe longitudinal stripes with a well defined wavelength, which evolve towards chevrons and scallops that interact and move again the <span class="hlt">dissolving</span> current. Thanks to a careful analysis of the competing physical mechanisms, we propose scaling laws, which account for the characteristic lengths and times of the early regime in experiments. The long-term evolution of patterns is understood qualitatively. A close related mechanism has been proposed to explain structures observed on the basal boundary of ice cover on brakish lakes [3] and we suggest that our experiments are analogous and explain the scallop-like patterns on iceberg walls. [1] P. Meakin and B. Jamtveit, Geological pattern formation by growth and dissolution in aqueous systems, Proc. R. Soc. A 466, 659-694 (2010). [2] P.N. Blumberg and R.L. Curl, Experimental and theoretical studies of dissolution roughness, J. Fluid Mech. 65, 735-751 (1974). [3] L. Solari and G. Parker, Morphodynamic modelling of the basal boundary of ice cover on brakish lakes, J.G.R. 118, 1432-1442 (2013).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5317162','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5317162"><span>Laser Calorimetry Spectroscopy for ppm-level <span class="hlt">Dissolved</span> Gas Detection and Analysis</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>K. S., Nagapriya; Sinha, Shashank; R., Prashanth; Poonacha, Samhitha; Chaudhry, Gunaranjan; Bhattacharya, Anandaroop; Choudhury, Niloy; Mahalik, Saroj; Maity, Sandip</p> <p>2017-01-01</p> <p>In this paper we report a newly developed technique – laser calorimetry spectroscopy (LCS), which is a combination of laser absorption spectroscopy and calorimetry - for the detection of gases <span class="hlt">dissolved</span> in liquids. The technique involves determination of <span class="hlt">concentration</span> of a <span class="hlt">dissolved</span> gas by irradiating the liquid with light of a wavelength where the gas absorbs, and measuring the temperature change caused by the absorbance. Conventionally, detection of <span class="hlt">dissolved</span> gases with sufficient sensitivity and specificity was done by first extracting the gases from the liquid and then analyzing the gases using techniques such as gas chromatography. Using LCS, we have been able to detect ppm levels of <span class="hlt">dissolved</span> gases without extracting them from the liquid. In this paper, we show the detection of <span class="hlt">dissolved</span> acetylene in transformer oil in the mid infrared (MIR) wavelength (3021 nm) region. PMID:28218304</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28218304','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28218304"><span>Laser Calorimetry Spectroscopy for ppm-level <span class="hlt">Dissolved</span> Gas Detection and Analysis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>K S, Nagapriya; Sinha, Shashank; R, Prashanth; Poonacha, Samhitha; Chaudhry, Gunaranjan; Bhattacharya, Anandaroop; Choudhury, Niloy; Mahalik, Saroj; Maity, Sandip</p> <p>2017-02-20</p> <p>In this paper we report a newly developed technique - laser calorimetry spectroscopy (LCS), which is a combination of laser absorption spectroscopy and calorimetry - for the detection of gases <span class="hlt">dissolved</span> in liquids. The technique involves determination of <span class="hlt">concentration</span> of a <span class="hlt">dissolved</span> gas by irradiating the liquid with light of a wavelength where the gas absorbs, and measuring the temperature change caused by the absorbance. Conventionally, detection of <span class="hlt">dissolved</span> gases with sufficient sensitivity and specificity was done by first extracting the gases from the liquid and then analyzing the gases using techniques such as gas chromatography. Using LCS, we have been able to detect ppm levels of <span class="hlt">dissolved</span> gases without extracting them from the liquid. In this paper, we show the detection of <span class="hlt">dissolved</span> acetylene in transformer oil in the mid infrared (MIR) wavelength (3021 nm) region.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1986/4190/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1986/4190/report.pdf"><span>Calibration of a <span class="hlt">dissolved</span>-solids model for the Yampa River basin between Steamboat Springs and Maybell, northwestern Colorado</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Parker, R.S.; Litke, D.W.</p> <p>1987-01-01</p> <p>The cumulative effects of changes in <span class="hlt">dissolved</span> solids from a number of coal mines are needed to evaluate effects on downstream water use. A model for determining cumulative effects of streamflow, <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span>, and <span class="hlt">dissolved</span>-solids load was calibrated for the Yampa River and its tributaries in northwestern Colorado. The model uses accounting principles. It establishes nodes on the stream system and sums water quantity and quality from node to node in the downstream direction. The model operates on a monthly time step for the study period that includes water years 1976 through 1981. Output is monthly mean streamflow, <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span>, and <span class="hlt">dissolved</span>-solids load. Streamflow and <span class="hlt">dissolved</span>-solids data from streamflow-gaging stations and other data-collection sites were used to define input data sets to initiate and to calibrate the model. The model was calibrated at four nodes and generally was within 10 percent of the observed values. The calibrated model can compute changes in <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> or load resulting from the cumulative effects of new coal mines or the expansion of old coal mines in the Yampa River basin. (USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26837382','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26837382"><span>Insight into <span class="hlt">dissolved</span> organic matter fractions in Lake Wivenhoe during and after a major flood.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Aryal, Rupak; Grinham, Alistair; Beecham, Simon</p> <p>2016-03-01</p> <p><span class="hlt">Dissolved</span> organic matter is an important component of biogeochemical processes in aquatic environments. <span class="hlt">Dissolved</span> organic matter may consist of a myriad of different fractions and resultant processing pathways. In early January 2011, heavy rainfall occurred across South East Queensland, Australia causing significant catchment inflow into Lake Wivenhoe, which is the largest water supply reservoir for the city of Brisbane, Australia. The horizontal and vertical distributions of <span class="hlt">dissolved</span> organic matter fractions in the lake during the flood period were investigated and then compared with stratified conditions with no catchment inflows. The results clearly demonstrate a large variation in <span class="hlt">dissolved</span> organic matter fractions associated with inflow conditions compared with stratified conditions. During inflows, <span class="hlt">dissolved</span> organic matter <span class="hlt">concentrations</span> in the reservoir were fivefold lower than during stratified conditions. Within the <span class="hlt">dissolved</span> organic matter fractions during inflow, the hydrophobic and humic acid fractions were almost half those recorded during the stratified period whilst low molecular weight neutrals were higher during the flood period compared to during the stratified period. Information on <span class="hlt">dissolved</span> organic matter and the spatial and vertical variations in its constituents' <span class="hlt">concentrations</span> across the lake can be very useful for catchment and lake management and for selecting appropriate water treatment processes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/40067','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/40067"><span>Seasonal ice and hydrologic controls on <span class="hlt">dissolved</span> organic carbon and nitrogen <span class="hlt">concentrations</span> in a boreal-rich fen</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Evan S. Kane; Merritt R. Turetsky; Jennifer W. Harden; A. David McGuire; James M. Waddington</p> <p>2010-01-01</p> <p>Boreal wetland carbon cycling is vulnerable to climate change in part because hydrology and the extent of frozen ground have strong influences on plant and microbial functions. We examined the response of <span class="hlt">dissolved</span> organic carbon (DOC) and total <span class="hlt">dissolved</span> nitrogen (TDN) across an experimental manipulation of water table position (both raised and lowered water table...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29516427','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29516427"><span>Coupling loss characteristics of runoff-sediment-adsorbed and <span class="hlt">dissolved</span> nitrogen and phosphorus on bare loess slope.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wu, Lei; Qiao, Shanshan; Peng, Mengling; Ma, Xiaoyi</p> <p>2018-05-01</p> <p>Soil and nutrient loss is a common natural phenomenon but it exhibits unclear understanding especially on bare loess soil with variable rainfall intensity and slope gradient, which makes it difficult to design control measures for agricultural diffuse pollution. We employ 30 artificial simulated rainfalls (six rainfall intensities and five slope gradients) to quantify the coupling loss correlation of runoff-sediment-adsorbed and <span class="hlt">dissolved</span> nitrogen and phosphorus on bare loess slope. Here, we show that effects of rainfall intensity on runoff yield was stronger than slope gradient with prolongation of rainfall duration, and the effect of slope gradient on runoff yield reduced gradually with increased rainfall intensity. But the magnitude of initial sediment yield increased significantly from an average value of 6.98 g at 5° to 36.08 g at 25° with increased slope gradient. The main factor of sediment yield would be changed alternately with the dual increase of slope gradient and rainfall intensity. <span class="hlt">Dissolved</span> total nitrogen (TN) and <span class="hlt">dissolved</span> total phosphorus (TP) <span class="hlt">concentrations</span> both showed significant fluctuations with rainfall intensity and slope gradient, and <span class="hlt">dissolved</span> TP <span class="hlt">concentration</span> was far less than <span class="hlt">dissolved</span> TN. Under the double influences of rainfall intensity and slope gradient, adsorbed TN <span class="hlt">concentration</span> accounted for 7-82% of TN loss <span class="hlt">concentration</span> with an average of 58.6% which was the main loss form of soil nitrogen, adsorbed TP <span class="hlt">concentration</span> accounted for 91.8-98.7% of TP loss <span class="hlt">concentration</span> with an average of 96.6% which was also the predominant loss pathway of soil phosphorus. Nitrate nitrogen (NO 3 - -N) accounted for 14.59-73.92% of <span class="hlt">dissolved</span> TN loss, and ammonia nitrogen (NH 4 + -N) accounted for 1.48-18.03%. NO 3 - -N was the main loss pattern of TN in runoff. Correlation between <span class="hlt">dissolved</span> TN, runoff yield, and rainfall intensity was obvious, and a significant correlation was also found between adsorbed TP, sediment yield, and slope gradient. Our</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5318914','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5318914"><span>Sensitivity of chemical weathering and <span class="hlt">dissolved</span> carbon dynamics to hydrological conditions in a typical karst river</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Zhong, Jun; Li, Si-liang; Tao, Faxiang; Yue, Fujun; Liu, Cong-Qiang</p> <p>2017-01-01</p> <p>To better understand the mechanisms that hydrological conditions control chemical weathering and carbon dynamics in the large rivers, we investigated hydrochemistry and carbon isotopic compositions of <span class="hlt">dissolved</span> inorganic carbon (DIC) based on high-frequency sampling in the Wujiang River draining the carbonate area in southwestern China. <span class="hlt">Concentrations</span> of major <span class="hlt">dissolved</span> solute do not strictly follow the dilution process with increasing discharge, and biogeochemical processes lead to variability in the <span class="hlt">concentration</span>-discharge relationships. Temporal variations of <span class="hlt">dissolved</span> solutes are closely related to weathering characteristics and hydrological conditions in the rainy seasons. The <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> carbon and the carbon isotopic compositions vary with discharge changes, suggesting that hydrological conditions and biogeochemical processes control <span class="hlt">dissolved</span> carbon dynamics. Biological CO2 discharge and intense carbonate weathering by soil CO2 should be responsible for the carbon variability under various hydrological conditions during the high-flow season. The <span class="hlt">concentration</span> of DICbio (DIC from biological sources) derived from a mixing model increases with increasing discharge, indicating that DICbio influx is the main driver of the chemostatic behaviors of riverine DIC in this typical karst river. The study highlights the sensitivity of chemical weathering and carbon dynamics to hydrological conditions in the riverine system. PMID:28220859</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70184409','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70184409"><span>Biogeochemical controls on diel cycling of stable isotopes of <span class="hlt">dissolved</span> 02 and <span class="hlt">dissolved</span> inorganic carbon in the Big Hole River, Montana</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Parker, Stephen R.; Poulson, Simon R.; Gammons, Christopher H.; DeGrandpre, Michael D.</p> <p>2005-01-01</p> <p>Rivers with high biological productivity typically show substantial increases in pH and <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span> during the day and decreases at night, in response to changes in the relative rates of aquatic photosynthesis and respiration. These changes, coupled with temperature variations, may impart diel (24-h) fluctuations in the <span class="hlt">concentration</span> of trace metals, nutrients, and other chemical species. A better understanding of diel processes in rivers is needed and will lead to improved methods of data collection for both monitoring and research purposes. Previous studies have used stable isotopes of <span class="hlt">dissolved</span> oxygen (DO) and <span class="hlt">dissolved</span> inorganic carbon (DIC) as tracers of geochemical and biological processes in streams, lakes, and marine systems. Although seasonal variation in δ18O of DO in rivers and lakes has been documented, no study has investigated diel changes in this parameter. Here, we demonstrate large (up to 13‰) cycles in δ18O-DO for two late summer sampling periods in the Big Hole River of southwest Montana and illustrate that these changes are correlated to variations in the DO <span class="hlt">concentration</span>, the C-isotopic composition of DIC, and the primary productivity of the system. The magnitude of the diel cycle in δ18O-DO was greater in August versus September because of the longer photoperiod and warmer water temperatures. This study provides another biogeochemical tool for investigating the O2 and C budgets in rivers and may also be applicable to lake and groundwater systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22421090','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22421090"><span>Measuring nonpolar organic contaminant partitioning in three Norwegian sediments using polyethylene passive samplers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Allan, Ian J; Ruus, Anders; Schaanning, Morten T; Macrae, Kenneth J; Næs, Kristoffer</p> <p>2012-04-15</p> <p><span class="hlt">Freely</span> <span class="hlt">dissolved</span> pore water <span class="hlt">concentrations</span> of polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), penta- and hexachlorobenzene (PeCB and HCB), octachlorostyrene (OCS), p,p'-DDE and p,p'-DDD were measured in bottom sediments from three sites in Norway. Sediments were from Aker Brygge, site of a former shipyard in the inner part of Oslofjord, Frierfjord in the Grenlandsfjord area, impacted during the 50 year-long activity of a magnesium smelter plant, and from Kristiansand harbour, site with high industrial activity. Low density polyethylene (LDPE) membrane samplers were exposed to these sediments in laboratory incubation under constant and low-level agitation for periods of 1, 2, 6, 13, 23 and 50 days. <span class="hlt">Freely</span> <span class="hlt">dissolved</span> pore water <span class="hlt">concentrations</span> were estimated from contaminant masses accumulated and sampling rates obtained from the measurement of kinetics of dissipation of performance reference compounds (PRCs). Marked differences in <span class="hlt">freely</span> <span class="hlt">dissolved</span> PAH <span class="hlt">concentrations</span> and resulting organic carbon-normalised sediment-pore water partition coefficients, logK(TOC), between these three sediments could be observed despite the generally similar total sediment <span class="hlt">concentrations</span>. In contrast with the PAH data, partitioning of PCBs and other organochlorine compounds (OCs) was relatively similar in all three sediments. For sediments from Frierfjord and Kristiansand, logK(TOC) values were lower for PCBs/OCs than for PAHs, indicating higher availability. Similar partitioning of PAHs and PCBs/OCs was found for sediments from Aker Brygge. No simple logK(oc)-logK(ow) relationships could model these data successfully. These results support the notion that the assessment of the risk posed by these compounds present in sediments in most cases requires actual measurement of contaminant availability. Copyright © 2012 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70189560','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70189560"><span><span class="hlt">Concentrations</span> and distributions of metals associated with <span class="hlt">dissolved</span> organic matter from the Suwannee River (GA, USA)</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kuhn, M. Keshia; Neubauer, Elisabeth; Hofmann, Thilo; von der Kammer, Frank; Aiken, George R.; Maurice, Patricia A.</p> <p>2015-01-01</p> <p><span class="hlt">Concentrations</span> and distributions of metals in Suwannee River (SR) raw filtered surface water (RFSW) and <span class="hlt">dissolved</span> organic matter (DOM) processed by reverse osmosis (RO), XAD-8 resin (for humic and fulvic acids [FA]), and XAD-4 resin (for “transphilic” acids) were analyzed by asymmetrical flow field-flow fractionation (AsFlFFF). SR samples were compared with DOM samples from Nelson's Creek (NLC), a wetland-draining stream in northern Michigan; previous International Humic Substances Society (IHSS) FA and RO samples from the SR; and an XAD-8 sample from Lake Fryxell (LF), Antarctica. Despite application of cation exchange during sample processing, all XAD and RO samples contained substantial metal <span class="hlt">concentrations</span>. AsFlFFF fractograms allowed metal distributions to be characterized as a function of DOM component molecular weight (MW). In SR RFSW, Fe, Al, and Cu were primarily associated with intermediate to higher than average MW DOM components. SR RO, XAD-8, and XAD-4 samples from May 2012 showed similar MW trends for Fe and Al but Cu tended to associate more with lower MW DOM. LF DOM had abundant Cu and Zn, perhaps due to amine groups that should be present due to its primarily algal origins. None of the fractograms showed obvious evidence for mineral nanoparticles, although some very small mineral nanoparticles might have been present at trace <span class="hlt">concentrations</span>. This research suggests that AsFlFFF is important for understanding how metals are distributed in different DOM samples (including IHSS samples), which may be key to metal reactivity and bioavailability.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70014892','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70014892"><span><span class="hlt">Dissolved</span> organic matter in anoxic pore waters from Mangrove Lake, Bermuda</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Orem, W.H.; Hatcher, P.G.; Spiker, E. C.; Szeverenyi, N.M.; Maciel, G.E.</p> <p>1986-01-01</p> <p><span class="hlt">Dissolved</span> organic matter and <span class="hlt">dissolved</span> inorganic chemical species in anoxic pore water from Mangrove Lake, Bermuda sediments were studied to evaluate the role of pore water in the early diagenesis of organic matter. <span class="hlt">Dissolved</span> sulphate, titration alkalinity, phosphate, and ammonia <span class="hlt">concentration</span> versus depth profiles were typical of many nearshore clastic sediments and indicated sulphate reduction in the upper 100 cm of sediment. The <span class="hlt">dissolved</span> organic matter in the pore water was made up predominantly of large molecules, was <span class="hlt">concentrated</span> from large quantities of pore water by using ultrafiltration and was extensively tudied by using elemental and stable carbon isotope analysis and high-resolution, solid state 13C nuclear magnetic resonance and infrared spectroscopy. The results indicate that this material has a predominantly polysaccharide-like structure and in addition contains a large amount of oxygen-containing functional groups (e.g., carboxyl groups). The 13C nulcear magnetic resonance spectra of the high-molecular-weight <span class="hlt">dissolved</span> organic matter resemble those of the organic matter in the surface sediments of Mangrove Lake. We propose that this high-molecular-weight organic matter in pore waters represents the partially degraded, labile organic components of the sedimentary organic matter and that pore waters serve as a conduit for removal of these labile organic components from the sediments. The more refractory components are, thus, selectively preserved in the sediments as humic substances (primarily humin). ?? 1986.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=140841&keyword=rosenberg&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=140841&keyword=rosenberg&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>RELATIONSHIPS BETWEEN NEAR-BOTTOM <span class="hlt">DISSOLVED</span> OXYGEN AND SEDIMENT PROFILE CAMERA MEASUREMENTS</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>The United States Environmental Protection Agency (U.S. EPA) and other environmental authorities regulate <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> oxygen (DO) as a measure of nutrient-related eutrophication in estuarine and coastal waters. However, in situ DO <span class="hlt">concentrations</span> are extremely var...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21707614','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21707614"><span><span class="hlt">Dissolved</span> oxygen as an indicator of bioavailable <span class="hlt">dissolved</span> organic carbon in groundwater.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chapelle, Francis H; Bradley, Paul M; McMahon, Peter B; Kaiser, Karl; Benner, Ron</p> <p>2012-01-01</p> <p><span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> oxygen (DO) plotted vs. <span class="hlt">dissolved</span> organic carbon (DOC) in groundwater samples taken from a coastal plain aquifer of South Carolina (SC) showed a statistically significant hyperbolic relationship. In contrast, DO-DOC plots of groundwater samples taken from the eastern San Joaquin Valley of California (CA) showed a random scatter. It was hypothesized that differences in the bioavailability of naturally occurring DOC might contribute to these observations. This hypothesis was examined by comparing nine different biochemical indicators of DOC bioavailability in groundwater sampled from these two systems. <span class="hlt">Concentrations</span> of DOC, total hydrolysable neutral sugars (THNS), total hydrolysable amino acids (THAA), mole% glycine of THAA, initial bacterial cell counts, bacterial growth rates, and carbon dioxide production/consumption were greater in SC samples relative to CA samples. In contrast, the mole% glucose of THNS and the aromaticity (SUVA(254)) of DOC was greater in CA samples. Each of these indicator parameters were observed to change with depth in the SC system in a manner consistent with active biodegradation. These results are uniformly consistent with the hypothesis that the bioavailability of DOC is greater in SC relative to CA groundwater samples. This, in turn, suggests that the presence/absence of a hyperbolic DO-DOC relationship may be a qualitative indicator of relative DOC bioavailability in groundwater systems. Ground Water © 2011, National Ground Water Association. Published 2011. This article is a U.S. Government work and is in the public domain in the USA.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016DSRI..116...77S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016DSRI..116...77S"><span><span class="hlt">Dissolved</span> low-molecular weight thiol <span class="hlt">concentrations</span> from the U.S. GEOTRACES North Atlantic Ocean zonal transect</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Swarr, Gretchen J.; Kading, Tristan; Lamborg, Carl H.; Hammerschmidt, Chad R.; Bowman, Katlin L.</p> <p>2016-10-01</p> <p>Low-molecular weight thiols, including cysteine and glutathione, are biomolecules involved in a variety of metabolic pathways and act as important antioxidant and metal buffering agents. In this last capacity, they represent a potential mechanism for modulating the bioavailability and biogeochemistry of many trace elements in the ocean, particularly for chalcophilic elements (e.g., Cu, Zn, Cd, Ag and Hg). For this reason, and in the context of the international GEOTRACES program that seeks to understand the biogeochemistry of trace elements in the ocean, we measured the <span class="hlt">concentration</span> of individual <span class="hlt">dissolved</span> low-molecular weight thiols during the U.S. GEOTRACES North Atlantic Zonal Transect (USGNAZT). Only two thiols were identified, cysteine and glutathione, in contrast to results from the northeast subarctic Pacific Ocean, where the dipeptides glycine-cysteine and arginine-cysteine were also present and γ-glutamylcysteine was dominant. <span class="hlt">Concentrations</span> of cysteine and glutathione in the North Atlantic Ocean were lower than in the Pacific and ranged from below detection ( 0.01 nM) to 0.61 nM of cysteine and up to 1.0 nM of glutathione, with cysteine generally more abundant than glutathione. Vertical profiles of cysteine and glutathione were broadly consistent with their biological production, being more abundant in surface water and usually below detection at depths greater than about 200 m. Subsurface <span class="hlt">concentration</span> maxima, often co-incident with the deep chlorophyll maximum, were frequently observed but not universal. We conclude that cysteine and glutathione do not make up significant portions of complexation capacity for Cu and Zn in the upper open ocean but could be important for Cd, Hg, and potentially other chalcophiles. Extremely low <span class="hlt">concentrations</span> of cysteine and glutathione in deep water suggest that higher molecular-weight thiols are a more important ligand class for chalcophiles in that portion of the ocean.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B41H2068M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B41H2068M"><span>Effect of photodegradation and biodegradation on the <span class="hlt">concentration</span> and composition of <span class="hlt">dissolved</span> organic matter in diverse waterbodies</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Manalilkada Sasidharan, S.; Dash, P.; Singh, S.; Lu, Y.</p> <p>2017-12-01</p> <p>The objective of this research was to quantify the effects of photodegradation and biodegradation on the <span class="hlt">dissolved</span> organic matter (DOM) <span class="hlt">concentration</span> and composition in five distinct waterbodies with diverse types of watershed land use and land cover in the southeastern United States. The water bodies included an agricultural pond, a lake in a predominantly forested watershed, a man-made reservoir, an estuary, and a bay. Two sets of samples were prepared from these water bodies by dispensing filtered water samples to unfiltered samples in 10:1 ratio. The first set was kept in the sunlight during the day (12 hours), and colored <span class="hlt">dissolved</span> organic matter (CDOM) absorption and fluorescence were measured periodically over a 30-day period for examining the effects of combined photo- and biodegradation. The second set of samples was kept in the dark for examining the effects of biodegradation alone, and CDOM absorption and fluorescence were measured at the same time as the sunlight-exposed samples. Subsequently, spectrometric results in tandem with multivariate statistical analysis were used to interpret the lability vs. composition of DOM. Parallel factor analysis (PARAFAC) revealed the presence of four DOM components (C1-C4). C1 and C4 were microbial tryptophan-like, labile lighter components, while C2 and C3 were terrestrial humic like or fulvic acid type, larger aromatic refractory components. The principal component analysis (PCA) also revealed two distinct groups of DOM - C1 and C4 vs. C2 and C3. The negative PC1 loadings of C2, C3, HIX, a254 and SUVA indicated humic-like or fulvic-like structurally complex refractory aromatic DOM originated from higher plants in forested areas. C1, C4, SR, FI and BI had positive PC1 loadings, which indicated structurally simpler labile DOM were derived from agricultural areas or microbial activity. There was a decrease in <span class="hlt">dissolved</span> organic carbon (DOC) due to combined photo- and biodegradation, and transformation of components C2</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26ES..121b2003L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26ES..121b2003L"><span>Prediction model of <span class="hlt">dissolved</span> oxygen in ponds based on ELM neural network</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Li, Xinfei; Ai, Jiaoyan; Lin, Chunhuan; Guan, Haibin</p> <p>2018-02-01</p> <p><span class="hlt">Dissolved</span> oxygen in ponds is affected by many factors, and its distribution is unbalanced. In this paper, in order to improve the imbalance of <span class="hlt">dissolved</span> oxygen distribution more effectively, the <span class="hlt">dissolved</span> oxygen prediction model of Extreme Learning Machine (ELM) intelligent algorithm is established, based on the method of improving <span class="hlt">dissolved</span> oxygen distribution by artificial push flow. Select the Lake Jing of Guangxi University as the experimental area. Using the model to predict the <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> of different voltage pumps, the results show that the ELM prediction accuracy is higher than the BP algorithm, and its mean square error is MSEELM=0.0394, the correlation coefficient RELM=0.9823. The prediction results of the 24V voltage pump push flow show that the discrete prediction curve can approximate the measured values well. The model can provide the basis for the artificial improvement of the <span class="hlt">dissolved</span> oxygen distribution decision.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_15 --> <div id="page_16" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="301"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29398550','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29398550"><span>Evaluation of the impact of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on biofilm microbial community in sequencing batch biofilm reactor.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Jingyin; Rong, Hongwei; Zhang, Chaosheng</p> <p>2018-05-01</p> <p>The effect of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (DO) during simultaneous nitrification and denitrification (SND) was investigated in a sequencing batch biofilm reactor (SBBR). In addition, the removal rates of nitrogen and bacterial communities were investigated under different <span class="hlt">concentrations</span> of DO (1.5, 3.5, and 4.5 mg/L). When the SND rate was 95.22%, the chemical oxygen demand and nitrogen removal was 92.22% and 84.15%, respectively, at 2.5 mg/L DO. The denitrification was inhibited by the increase of oxygen <span class="hlt">concentration</span>. Microelectrode measurements showed that the thickness of oxygen penetration increased from 1.0 mm to 2.7 mm when the DO <span class="hlt">concentration</span> increased from 1.5 mg/L to 5.5 mg/L. The current location of the aerobic and anaerobic layers in the biofilm was determined for analysis of the microbial community. High-throughput sequencing analysis revealed the communities of the biofilm approached similar structure and composition. Uliginosibacterium species, biofilm-forming bacteria Zoogloea species and Acinetobacter species were dominant. In the aerobic layer, phyla Betaproteobacteria and Saprospirae were predominant, the major phyla were shifted from Proteobacteria followed by Firmicutes and Bacteroidetes, which comprised 82% of the total sequences during the SND period. Anaerolineae was dominated in the anaerobic layer. The high abundance of Nitrospira in the aerobic biofilm provides evidence of the SND system performing better at ammonia oxidization. In addition, real-time PCR indicated that the amount of ammonia-oxidizing bacteria (AOB) and nitrite-oxidizing bacteria (NOB) matched the Nitrospirales and Nitrosomonadales abundance well. Collectively, this study demonstrated the dynamics of key bacterial communities in the SND system were highly influenced by the DO <span class="hlt">concentration</span>. Copyright © 2017 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24998780','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24998780"><span>Emotions in <span class="hlt">freely</span> varying and mono-pitched vowels, acoustic and EGG analyses.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Waaramaa, Teija; Palo, Pertti; Kankare, Elina</p> <p>2015-12-01</p> <p>Vocal emotions are expressed either by speech or singing. The difference is that in singing the pitch is predetermined while in speech it may vary <span class="hlt">freely</span>. It was of interest to study whether there were voice quality differences between <span class="hlt">freely</span> varying and mono-pitched vowels expressed by professional actors. Given their profession, actors have to be able to express emotions both by speech and singing. Electroglottogram and acoustic analyses of emotional utterances embedded in expressions of <span class="hlt">freely</span> varying vowels [a:], [i:], [u:] (96 samples) and mono-pitched protracted vowels (96 samples) were studied. Contact quotient (CQEGG) was calculated using 35%, 55%, and 80% threshold levels. Three different threshold levels were used in order to evaluate their effects on emotions. Genders were studied separately. The results suggested significant gender differences for CQEGG 80% threshold level. SPL, CQEGG, and F4 were used to convey emotions, but to a lesser degree, when F0 was predetermined. Moreover, females showed fewer significant variations than males. Both genders used more hypofunctional phonation type in mono-pitched utterances than in the expressions with <span class="hlt">freely</span> varying pitch. The present material warrants further study of the interplay between CQEGG threshold levels and formant frequencies, and listening tests to investigate the perceptual value of the mono-pitched vowels in the communication of emotions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/36166','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/36166"><span>Stream <span class="hlt">dissolved</span> organic matter bioavailability and composition in watersheds underlain with discontinuous permafrost</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Kelly L. Balcarczyk; Jeremy B. Jones; Rudolf Jaffe; Nagamitsu Maie</p> <p>2009-01-01</p> <p>We examined the impact of permafrost on <span class="hlt">dissolved</span> organic matter (DOM) composition in Caribou-Poker Creeks Research Watershed (CPCRW), a watershed underlain with discontinuous permafrost, in interior Alaska. The stream draining the high permafrost watershed had higher DOC and <span class="hlt">dissolved</span> organic nitrogen (DON) <span class="hlt">concentrations</span>, higher DOCDON and greater specific...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28628819','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28628819"><span><span class="hlt">Dissolved</span> gaseous mercury formation and mercury volatilization in intertidal sediments.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cesário, Rute; Poissant, Laurier; Pilote, Martin; O'Driscoll, Nelson J; Mota, Ana M; Canário, João</p> <p>2017-12-15</p> <p>Intertidal sediments of Tagus estuary regularly experiences complex redistribution due to tidal forcing, which affects the cycling of mercury (Hg) between sediments and the water column. This study quantifies total mercury (Hg) and methylmercury (MMHg) <span class="hlt">concentrations</span> and fluxes in a flooded mudflat as well as the effects on water-level fluctuations on the air-surface exchange of mercury. A fast increase in <span class="hlt">dissolved</span> Hg and MMHg <span class="hlt">concentrations</span> was observed in overlying water in the first 10min of inundation and corresponded to a decrease in pore waters, suggesting a rapid export of Hg and MMHg from sediments to the water column. Estimations of daily advective transport exceeded the predicted diffusive fluxes by 5 orders of magnitude. A fast increase in <span class="hlt">dissolved</span> gaseous mercury (DGM) <span class="hlt">concentration</span> was also observed in the first 20-30min of inundation (maximum of 40pg L -1 ). Suspended particulate matter (SPM) <span class="hlt">concentrations</span> were inversely correlated with DGM <span class="hlt">concentrations</span>. <span class="hlt">Dissolved</span> Hg variation suggested that biotic DGM production in pore waters is a significant factor in addition to the photochemical reduction of Hg. Mercury volatilization (ranged from 1.1 to 3.3ngm -2 h -1 ; average of 2.1ngm -2 h -1 ) and DGM production exhibited the same pattern with no significant time-lag suggesting a fast release of the produced DGM. These results indicate that Hg sediment/water exchanges in the physical dominated estuaries can be underestimated when the tidal effect is not considered. Copyright © 2017 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JGRG..119.1919A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JGRG..119.1919A"><span>Qualitative changes of riverine <span class="hlt">dissolved</span> organic matter at low salinities due to flocculation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Asmala, Eero; Bowers, David G.; Autio, Riitta; Kaartokallio, Hermanni; Thomas, David N.</p> <p>2014-10-01</p> <p>The flocculation of <span class="hlt">dissolved</span> organic matter (DOM) was studied along transects through three boreal estuaries. Besides the bulk <span class="hlt">concentration</span> parameters, a suite of DOM quality parameters were investigated, including colored DOM (CDOM), fluorescent DOM, and the molecular weight of DOM as well as associated <span class="hlt">dissolved</span> iron <span class="hlt">concentrations</span>. We observed significant deviations from conservative mixing at low salinities (<2) in the estuarine samples of <span class="hlt">dissolved</span> organic carbon (DOC), UV absorption (a(CDOM254)), and humic-like fluorescence. The maximum deviation from conservative mixing for DOC <span class="hlt">concentration</span> was -16%, at salinities between 1 and 2. An associated laboratory experiment was conducted where an artificial salinity gradient between 0 and 6 was created. The experiment confirmed the findings from the estuarine transects, since part of the DOC and <span class="hlt">dissolved</span> iron pools were transformed to particulate fraction (>0.2 µm) and thereby removing them from the <span class="hlt">dissolved</span> phase. We also measured flocculation of CDOM, especially in the UV region of the absorption spectrum. Protein-like fluorescence of DOM decreased, while humic-like fluorescence increased because of salt-induced flocculation. Additionally, there was a decrease in molecular weight of DOM. Consequently, the quantity and quality of the remaining DOM pool was significantly changed after influenced to flocculation. Based on these results, we constructed a mechanistic, two-component flocculation model. Our findings underline the importance of the coastal filter, where riverine organic matter is flocculated and exported to the sediments.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009EGUGA..11.4283D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009EGUGA..11.4283D"><span>A new device for continuous monitoring the CO2 <span class="hlt">dissolved</span> in water</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>de Gregorio, S.; Camarda, M.; Cappuzzo, S.; Giudice, G.; Gurrieri, S.; Longo, M.</p> <p>2009-04-01</p> <p>The measurements of <span class="hlt">dissolved</span> CO2 in water are common elements of industrial processes and scientific research. In order to perform gas <span class="hlt">dissolved</span> measurements is required to separate the <span class="hlt">dissolved</span> gaseous phase from water. We developed a new device able to separate the gases phase directly in situ and well suitable for continuous measuring the CO2 <span class="hlt">dissolved</span> in water. The device is made by a probe of a polytetrafluorethylene (PTFE) tube connected to an I.R. spectrophotometer (I.R.) and a pump. The PTFE is a polymeric semi-permeable membrane and allows the permeation of gas in the system. Hence, this part of the device is dipped in water in order to equilibrate the probe headspace with the <span class="hlt">dissolved</span> gases. The partial pressure of the gas i in the headspace at equilibrium (Pi) follows the Henry's law: Pi=Hi•Ci, where Hi is the Henry's constant and Ci is the <span class="hlt">dissolved</span> <span class="hlt">concentration</span> of gas i. After the equilibrium is achieved, the partial pressure of CO2 inside the tube is equal to the partial pressure of <span class="hlt">dissolved</span> CO2. The <span class="hlt">concentration</span> of CO2 is measured by the I.R. connected to the tube. The gas is moved from the tube headspace to the I.R. by using the pump. In order to test the device and assess the best operating condition, several experimental were performed in laboratory. All the test were executed in a special apparatus where was feasible to create controlled atmospheres. Afterward the device has been placed in a draining tunnel sited in the Mt. Etna Volcano edifice (Italy). The monitored groundwater intercepts the Pernicana Fault, along which degassing phenomena are often observed. The values recorded by the station result in agreement with monthly directly measurements of <span class="hlt">dissolved</span> CO2 partial pressure.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1989/4047/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1989/4047/report.pdf"><span>Water resources and effects of potential surface coal mining on <span class="hlt">dissolved</span> solids in Hanging Woman Creek basin, southeastern Montana</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Cannon, M.R.</p> <p>1989-01-01</p> <p>Groundwater resources of the Hanging Woman Creek basin, Montana include Holocene and Pleistocene alluvial aquifers and sandstone , coal, and clinker aquifers in the Paleocene Fort Union Formation. Surface water resources are composed of Hanging Woman Creek, its tributaries, and small stock ponds. <span class="hlt">Dissolved</span>-solids <span class="hlt">concentrations</span> in groundwater ranged from 200 to 11,00 mg/L. Generally, <span class="hlt">concentrations</span> were largest in alluvial aquifers and smallest in clinker aquifers. Near its mouth, Hanging Woman Creek had a median <span class="hlt">concentration</span> of about 1,800 mg/L. Mining of the 20-foot to 35-foot-thick Anderson coal bed and 3-foot to 16-foot thick Dietz coal bed could increase <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> in shallow aquifers and in Hanging Woman Creek because of leaching of soluble minerals from mine spoils. Analysis of saturated-paste extracts from 158 overburden samples indicated that water moving through mine spoils would have a median increase in <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> of about 3,700 mg/L, resulting in an additional <span class="hlt">dissolved</span>-solids load to Hanging Woman Creek of about 3.0 tons/day. Hanging Woman Creek near Birney could have an annual post-mining <span class="hlt">dissolved</span>-solids load of 3,415 tons at median discharge, a 47% increase from pre-mining conditions load. Post-mining <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids, at median discharge, could range from 2,380 mg/L in March to 3,940 mg/L in August, compared to mean pre-mining <span class="hlt">concentrations</span> that ranged from 1,700 mg/L in July, November, and December to 2,060 mg/L in May. Post-mining <span class="hlt">concentrations</span> and loads in Hanging Woman Creek would be smaller if a smaller area were mined. (USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/of/2014/1209/pdf/ofr2014-1209.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/of/2014/1209/pdf/ofr2014-1209.pdf"><span><span class="hlt">Concentration</span> and flux of total and <span class="hlt">dissolved</span> phosphorus, total nitrogen, chloride, and total suspended solids for monitored tributaries of Lake Champlain, 1990-2012</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Medalie, Laura</p> <p>2014-01-01</p> <p>Annual and daily <span class="hlt">concentrations</span> and fluxes of total and <span class="hlt">dissolved</span> phosphorus, total nitrogen, chloride, and total suspended solids were estimated for 18 monitored tributaries to Lake Champlain by using the Weighted Regressions on Time, Discharge, and Seasons regression model. Estimates were made for 21 or 23 years, depending on data availability, for the purpose of providing timely and accessible summary reports as stipulated in the 2010 update to the Lake Champlain “Opportunities for Action” management plan. Estimates of <span class="hlt">concentration</span> and flux were provided for each tributary based on (1) observed daily discharges and (2) a flow-normalizing procedure, which removed the random fluctuations of climate-related variability. The flux bias statistic, an indicator of the ability of the Weighted Regressions on Time, Discharge, and Season regression models to provide accurate representations of flux, showed acceptable bias (less than ±10 percent) for 68 out of 72 models for total and <span class="hlt">dissolved</span> phosphorus, total nitrogen, and chloride. Six out of 18 models for total suspended solids had moderate bias (between 10 and 30 percent), an expected result given the frequently nonlinear relation between total suspended solids and discharge. One model for total suspended solids with a very high bias was influenced by a single extreme value; however, removal of that value, although reducing the bias substantially, had little effect on annual fluxes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016JMS...155...84C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016JMS...155...84C"><span>Sources, behaviors and degradation of <span class="hlt">dissolved</span> organic matter in the East China Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Chen, Yan; Yang, Gui-Peng; Liu, Li; Zhang, Peng-Yan; Leng, Wei-Song</p> <p>2016-03-01</p> <p><span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> organic carbon (DOC), <span class="hlt">dissolved</span> inorganic nitrogen (DIN), <span class="hlt">dissolved</span> organic nitrogen (DON) and its major compound classes-total hydrolysable amino acids (THAA) were measured at 4 cross-shelf transects of the East China Sea in July 2011. Surface <span class="hlt">concentrations</span> of DOC, DIN, DON and THAA at the nearshore stations were mostly in excess of those found at the offshore sites, indicating either substantial autochthonous production or allochthonous inputs from the Changjiang River. The vertical distributions of DOC, DON and THAA showed similar trends with higher values in the surface layer, whereas the elevated <span class="hlt">concentrations</span> of DIN were observed in the bottom layer. Major constituents of THAA presented in the study area were glycine, serine, alanine, glutamic acid, aspartic acid and valine. The mole percentages of neutral amino acids increased from surface water to bottom water, whereas acidic and hydroxy amino acids decreased with the water depth. <span class="hlt">Concentrations</span> of DOC and THAA were negatively correlated to the ΔDIN values (the difference between the real <span class="hlt">concentration</span> and theoretical <span class="hlt">concentration</span>), respectively, indicating the coupling relation between <span class="hlt">dissolved</span> organic matter (DOM) remineralization and nutrient regeneration in the water column. The C/N ratios in the water column exhibited different characteristics with elevated values appearing in the surface and bottom layers. Box and whisker plots showed that both degradation index (DI) values and THAA yields displayed a decreasing trend from the surface layer to the bottom layer, implying increasing degradation with the water depth. Our data revealed that glycine and alanine increased in relative abundance with decreasing DI, while tyrosine, valine, phenylalanine and isoleucine increased with increasing DI.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JMS...138...51B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JMS...138...51B"><span>Seasonal and interannual variability of <span class="hlt">dissolved</span> oxygen around the Balearic Islands from hydrographic data</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Balbín, R.; López-Jurado, J. L.; Aparicio-González, A.; Serra, M.</p> <p>2014-10-01</p> <p>Oceanographic data obtained between 2001 and 2011 by the Spanish Institute of Oceanography (IEO, Spain) have been used to characterise the spatial distribution and the temporal variability of the <span class="hlt">dissolved</span> oxygen around the Balearic Islands (Mediterranean Sea). The study area includes most of the Western Mediterranean Sea, from the Alboran Sea to Cape Creus, at the border between France and Spain. <span class="hlt">Dissolved</span> oxygen (DO) at the water surface is found to be in a state of equilibrium exchange with the atmosphere. In the spring and summer a subsurface oxygen supersaturation is observed due to the biological activity, above the subsurface fluorescence maximum. Minimum observed values of <span class="hlt">dissolved</span> oxygen are related to the Levantine Intermediate Waters (LIW). An unusual minimum of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> was also recorded in the Alboran Sea Oxygen Minimum Zone. The Western Mediterranean Deep Waters (WMDW) and the Western Intermediate Waters (WIW) show higher values of <span class="hlt">dissolved</span> oxygen than the Levantine Intermediate Waters due to their more recent formation. Using these <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> it is possible to show that the Western Intermediate Waters move southwards across the Ibiza Channel and the deep water circulates around the Balearic Islands. It has also been possible to characterise the seasonal evolution of the different water masses and their <span class="hlt">dissolved</span> oxygen content in a station in the Algerian sub-basin.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26270047','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26270047"><span>A <span class="hlt">Dissolved</span> Oxygen Threshold for Shifts in Bacterial Community Structure in a Seasonally Hypoxic Estuary.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Spietz, Rachel L; Williams, Cheryl M; Rocap, Gabrielle; Horner-Devine, M Claire</p> <p>2015-01-01</p> <p>Pelagic ecosystems can become depleted of <span class="hlt">dissolved</span> oxygen as a result of both natural processes and anthropogenic effects. As <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> decreases, energy shifts from macrofauna to microorganisms, which persist in these hypoxic zones. Oxygen-limited regions are rapidly expanding globally; however, patterns of microbial communities associated with <span class="hlt">dissolved</span> oxygen gradients are not yet well understood. To assess the effects of decreasing <span class="hlt">dissolved</span> oxygen on bacteria, we examined shifts in bacterial community structure over space and time in Hood Canal, Washington, USA-a glacial fjord-like water body that experiences seasonal low <span class="hlt">dissolved</span> oxygen levels known to be detrimental to fish and other marine organisms. We found a strong negative association between bacterial richness and <span class="hlt">dissolved</span> oxygen. Bacterial community composition across all samples was also strongly associated with the <span class="hlt">dissolved</span> oxygen gradient, and significant changes in bacterial community composition occurred at a <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> between 5.18 and 7.12 mg O2 L(-1). This threshold value of <span class="hlt">dissolved</span> oxygen is higher than classic definitions of hypoxia (<2.0 mg O2 L(-1)), suggesting that changes in bacterial communities may precede the detrimental effects on ecologically and economically important macrofauna. Furthermore, bacterial taxa responsible for driving whole community changes across the oxygen gradient are commonly detected in other oxygen-stressed ecosystems, suggesting that the patterns we uncovered in Hood Canal may be relevant in other low oxygen ecosystems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4535773','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4535773"><span>A <span class="hlt">Dissolved</span> Oxygen Threshold for Shifts in Bacterial Community Structure in a Seasonally Hypoxic Estuary</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Spietz, Rachel L.; Williams, Cheryl M.; Rocap, Gabrielle; Horner-Devine, M. Claire</p> <p>2015-01-01</p> <p>Pelagic ecosystems can become depleted of <span class="hlt">dissolved</span> oxygen as a result of both natural processes and anthropogenic effects. As <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> decreases, energy shifts from macrofauna to microorganisms, which persist in these hypoxic zones. Oxygen-limited regions are rapidly expanding globally; however, patterns of microbial communities associated with <span class="hlt">dissolved</span> oxygen gradients are not yet well understood. To assess the effects of decreasing <span class="hlt">dissolved</span> oxygen on bacteria, we examined shifts in bacterial community structure over space and time in Hood Canal, Washington, USA−a glacial fjord-like water body that experiences seasonal low <span class="hlt">dissolved</span> oxygen levels known to be detrimental to fish and other marine organisms. We found a strong negative association between bacterial richness and <span class="hlt">dissolved</span> oxygen. Bacterial community composition across all samples was also strongly associated with the <span class="hlt">dissolved</span> oxygen gradient, and significant changes in bacterial community composition occurred at a <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> between 5.18 and 7.12 mg O2 L-1. This threshold value of <span class="hlt">dissolved</span> oxygen is higher than classic definitions of hypoxia (<2.0 mg O2 L-1), suggesting that changes in bacterial communities may precede the detrimental effects on ecologically and economically important macrofauna. Furthermore, bacterial taxa responsible for driving whole community changes across the oxygen gradient are commonly detected in other oxygen-stressed ecosystems, suggesting that the patterns we uncovered in Hood Canal may be relevant in other low oxygen ecosystems. PMID:26270047</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016FrEaS...4...58V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016FrEaS...4...58V"><span>Response of <span class="hlt">dissolved</span> carbon and nitrogen <span class="hlt">concentrations</span> to moderate nutrient additions in a tropical montane forest of south Ecuador</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Velescu, Andre; Valarezo, Carlos; Wilcke, Wolfgang</p> <p>2016-05-01</p> <p>In the past two decades, the tropical montane rain forests in south Ecuador experienced increasing deposition of reactive nitrogen mainly originating from Amazonian forest fires, while Saharan dust inputs episodically increased deposition of base metals. Increasing air temperature and unevenly distributed rainfall have allowed for longer dry spells in a perhumid ecosystem. This might have favored mineralization of <span class="hlt">dissolved</span> organic matter (DOM) by microorganisms and increased nutrient release from the organic layer. Environmental change is expected to impact the functioning of this ecosystem belonging to the biodiversity hotspots of the Earth. In 2007, we established a nutrient manipulation experiment (NUMEX) to understand the response of the ecosystem to moderately increased nutrient inputs. Since 2008, we have continuously applied 50 kg ha-1 a-1 of nitrogen (N), 10 kg ha-1 a-1 of phosphorus (P), 50 kg + 10 kg ha-1 a-1 of N and P and 10 kg ha-1 a-1 of calcium (Ca) in a randomized block design at 2000 m a.s.l. in a natural forest on the Amazonia-exposed slopes of the south Ecuadorian Andes. Nitrogen <span class="hlt">concentrations</span> in throughfall increased following N+P additions, while separate N amendments only increased nitrate <span class="hlt">concentrations</span>. Total organic carbon (TOC) and <span class="hlt">dissolved</span> organic nitrogen (DON) <span class="hlt">concentrations</span> showed high seasonal variations in litter leachate and decreased significantly in the P and N+P treatments, but not in the N treatment. Thus, P availability plays a key role in the mineralization of DOM. TOC/DON ratios were narrower in throughfall than in litter leachate but their temporal course did not respond to nutrient amendments. Our results revealed an initially fast, positive response of the C and N cycling to nutrient additions which declined with time. TOC and DON cycling only change if N and P supply are improved concurrently, while NO3-N leaching increases only if N is separately added. This indicates co-limitation of the microorganisms by N and P</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016JPhCS.704a2009G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016JPhCS.704a2009G"><span>Amphiphilic Fluorinated Polymer Nanoparticle Film Formation and <span class="hlt">Dissolved</span> Oxygen Sensing Application</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gao, Yu; Zhu, Huie; Yamamoto, Shunsuke; Miyashita, Tokuji; Mitsuishi, Masaya</p> <p>2016-04-01</p> <p>Fluorinated polymer nanoparticle films were prepared by <span class="hlt">dissolving</span> amphiphilic fluorinated polymer, poly (N-1H, 1H-pentadecafluorooctylmethacrylamide) (pC7F15MAA) in two miscible solvents (AK-225 and acetic acid). A superhydrophobic and porous film was obtained by dropcasting the solution on substrates. With higher ratios of AK-225 to acetic acid, pC7F15MAA was densified around acetic acid droplets, leading to the formation of pC7F15MAA nanoparticles. The condition of the nanoparticle film preparation was investigated by varying the mixing ratio or total <span class="hlt">concentration</span>. A highly sensitive <span class="hlt">dissolved</span> oxygen sensor system was successfully prepared utilizing a smart surface of superhydrophobic and porous pC7F15MAA nanoparticle film. The sensitivity showed I0/I40 = 126 in the range of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> of 0 ~ 40 mg L-1. The oxygen sensitivity was compared with that of previous reports.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/15382849','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/15382849"><span>Factors affecting the presence of <span class="hlt">dissolved</span> glutathione in estuarine waters.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tang, Degui; Shafer, Martin M; Karner, Dawn A; Overdier, Joel; Armstrong, David E</p> <p>2004-08-15</p> <p>We investigated factors influencing the presence of the thiol glutathione (GSH) in estuarine waters. Our study addressed thiol phase-association, the biological release from algal cultures, and the role of copper in both thiol release and preservation. Our measurements in three diverse estuaries in the continental United States (San Diego Bay, Cape Fear Estuary, and Norfolk Estuary) show that <span class="hlt">dissolved</span> GSH, present at sub-nanomolar levels, is preferentially partitioned into the ultra-filtrate fraction (<1 kDa) in comparison with <span class="hlt">dissolved</span> organic carbon (DOC). <span class="hlt">Concentrations</span> of GSH generally increased with increases in total copper (Cu)levels, although large variability was observed among estuaries. In 30-h exposure experiments, release of <span class="hlt">dissolved</span> GSH from the diatom Thalassiosira weissflogii into organic ligand-free experimental media was a strong function of added Cu <span class="hlt">concentration</span>. The released GSH increased from about 0.02 to 0.27 fmol/cell as Cu was increased from the background level (0.5 nM) to 310 nM in the modified Aquil media. However, excretion of GSH was lower (up to 0.13 fmol/cell) when cells were grown in surface waters of San Diego Bay, despite much higher total Cu <span class="hlt">concentrations</span>. Experiments conducted in-situ in San Diego Bay water indicated that high <span class="hlt">concentrations</span> of added Cu destabilized GSH, while both Mn(II) and natural colloids promoted GSH stability. In contrast, laboratory experiments in synthetic media indicated that moderate levels of added Cu enhanced GSH stability.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28419978','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28419978"><span><span class="hlt">Dissolved</span> oxygen, stream temperature, and fish habitat response to environmental water purchases.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Null, Sarah E; Mouzon, Nathaniel R; Elmore, Logan R</p> <p>2017-07-15</p> <p>Environmental water purchases are increasingly used for ecological protection. In Nevada's Walker Basin (western USA), environmental water purchases augment streamflow in the Walker River and increase lake elevation of terminal Walker Lake. However, water quality impairments like elevated stream temperatures and low <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> also limit ecosystems and species, including federally-threatened Lahontan cutthroat trout. In this paper, we prioritize water volumes and locations that most enhance water quality for riverine habitat from potential environmental water rights purchases. We monitored and modeled streamflows, stream temperatures, and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> using River Modeling System, an hourly, physically-based hydrodynamic and water quality model. Modeled environmental water purchases ranged from average daily increases of 0.11-1.41 cubic meters per second (m 3 /s) during 2014 and 2015, two critically dry years. Results suggest that water purchases consistently cooled maximum daily stream temperatures and warmed nightly minimum temperatures. This prevented extremely low <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> below 5.0 mg/L, but increased the duration of moderate conditions between 5.5 and 6.0 mg/L. Small water purchases less than approximately 0.71 m 3 /s per day had little benefit for Walker River habitat. <span class="hlt">Dissolved</span> oxygen <span class="hlt">concentrations</span> were affected by upstream environmental conditions, where suitable upstream water quality improved downstream conditions and vice versa. Overall, this study showed that critically dry water years degrade environmental water quality and habitat, but environmental water purchases of at least 0.71 m 3 /s were promising for river restoration. Published by Elsevier Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011SPIE.8175E..1AQ','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011SPIE.8175E..1AQ"><span>Relationship between the colored <span class="hlt">dissolved</span> organic matter and <span class="hlt">dissolved</span> organic carbon and the application on remote sensing in East China Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Qiong, Liu; Pan, Delu; Huang, Haiqing; Lu, Jianxin; Zhu, Qiankun</p> <p>2011-11-01</p> <p>A cruise was conducted in the East China Sea (ECS) in autumn 2010 to collect <span class="hlt">Dissolved</span> Organic Carbon (DOC) and Colored <span class="hlt">Dissolved</span> Organic Matter (CDOM) samples. The distribution of DOC mainly controlled by the hydrography since the relationship between DOC and salinity was significant in both East China Sea. The biological activity had a significant influence on the <span class="hlt">concentration</span> of DOC with a close correlation between DOC and Chl a. The absorption coefficient of CDOM (a355) decreased with the salinity increasing in the shelf of East China Sea (R2=0.9045). CDOM and DOC were significantly correlated in ECS where DOC distribution was dominated largely by the Changjiang diluted water. Based on the relationship of CDOM and DOC, we estimated the DOC <span class="hlt">concentration</span> of the surface in ECS from satellite-derived CDOM images. Some deviations induced by the biological effect and related marine DOC accumulations were discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003fslc.book.....S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003fslc.book.....S"><span><span class="hlt">Freely</span> Suspended Liquid Crystalline Films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sonin, A. A.</p> <p>2003-05-01</p> <p><span class="hlt">Freely</span> Suspended Liquid Crystalline Films Andrei A. Sonin Centre d'Etudes Atomiques de Saclay, France and Institute of Crystallography, Russian Academy of Sciences with a Foreword by Professor Noel Clark University of Colorado, USA This book provides a brief introduction to the physics of liquid crystals and to macroscopic physical parameters characterising <span class="hlt">freely</span> suspended liquid crystalline (FSLC) films, and then reviews the experimental techniques for preparing these films, measuring their thicknesses, and investigating their physical properties and structural aspects. Molecular structures and defects of FSLC films and the problems of film stability, thinning and rupture are discussed in later chapters. Physical phenomena, such as orientational and phase transitions, Frederick's and flexoelectric effects, hydroelectrodynamics, etc., are also analysed. Finally, some applications of FSLC films in industry and in various branches of science are discussed. Specialists working in the physics of liquid crystals and in surface physics will find this book of interest. Industrial firms and their research centres investigating liquid crystals, biological membranes, detergent/surfactant/biomedical areas; and graduates and postgraduates in solid state physics and crystallography will also benefit from this book. The book has an easy-to-read style with just the minimum amount of mathematics necessary to explain important concepts. This is the first book dedicated exclusively to the physics of FSLC in almost a century since their discovery and last twenty years of their active studies. Andrei Sonin, a scientist in the area of FSLC and author of many articles on surface phenomena in liquid crystals, the properties and behaviour of thin liquid crystalline and surfactant films, has a long standing reputation in liquid crystals and surfactant systems and has been particularly active in issues involving surface interactions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/of/2013/1190/pdf/ofr2013-1190.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/of/2013/1190/pdf/ofr2013-1190.pdf"><span>Knowledge and understanding of <span class="hlt">dissolved</span> solids in the Rio Grande–San Acacia, New Mexico, to Fort Quitman, Texas, and plan for future studies and monitoring</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Moyer, Douglas; Anderholm, Scott K.; Hogan, James F.; Phillips, Fred M.; Hibbs, Barry J.; Witcher, James C.; Matherne, Anne Marie; Falk, Sarah E.</p> <p>2013-01-01</p> <p>-Focused Hydrogeology Studies at Inflow Sources: Map <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> in the Rio Grande and underlying alluvial aquifer; perform hydrogeologic characterization of subsurface areas containing unusually high <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids. -Modeling of <span class="hlt">Dissolved</span> Solids: Develop models to simulate the transport and storage of <span class="hlt">dissolved</span> solids in both surface-water and groundwater systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19064278','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19064278"><span>Export of <span class="hlt">dissolved</span> organic matter in relation to land use along a European climatic gradient.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mattsson, Tuija; Kortelainen, Pirkko; Laubel, Anker; Evans, Dylan; Pujo-Pay, Mireille; Räike, Antti; Conan, Pascal</p> <p>2009-03-01</p> <p>The terrestrial export of <span class="hlt">dissolved</span> organic matter (DOM) is associated with climate, vegetation and land use, and thus is under the influence of climatic variability and human interference with terrestrial ecosystems, their soils and hydrological cycles. We present a data-set including catchments from four areas covering the major climate and land use gradients within Europe: a forested boreal zone (Finland), a temperate agricultural area (Denmark), a wet and temperate mountain region in Wales, and a warm Mediterranean catchment draining into the Gulf of Lyon. In all study areas, DOC (<span class="hlt">dissolved</span> organic carbon) was a major fraction of DOM, with much lower proportions of DON (<span class="hlt">dissolved</span> organic nitrogen) and DOP (<span class="hlt">dissolved</span> organic phosphorus). A south-north gradient with highest DOC <span class="hlt">concentrations</span> and export in the northernmost catchments was recorded: DOC <span class="hlt">concentrations</span> and loads were highest in Finland and lowest in France. These relationships indicate that DOC <span class="hlt">concentrations</span>/export are controlled by several factors including wetland and forest cover, precipitation and hydrological processes. DON <span class="hlt">concentrations</span> and loads were highest in the Danish catchments and lowest in the French catchments. In Wales and Finland, DON <span class="hlt">concentrations</span> increased with the increasing proportion of agricultural land in the catchment, whereas in Denmark and France no such relationship was found. DOP <span class="hlt">concentrations</span> and loads were low compared to DOC and DON. The highest DOP <span class="hlt">concentrations</span> and loads were recorded in catchments with a high extent of agricultural land, large urban areas or a high population density, reflecting the influence of human impact on DOP loads.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_16 --> <div id="page_17" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="321"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1987/4024/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1987/4024/report.pdf"><span>Assessment of water quality and factors affecting <span class="hlt">dissolved</span> oxygen in the Sangamon River, Decatur to Riverton, Illinois, summer 1982</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Schmidt, A.R.; Stamer, J.K.</p> <p>1987-01-01</p> <p>Water quality and processes that affect the <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> in a 45.9 mile reach of the Sangamon River from Decatur to Riverton, Illinois, were determined from data collected during low-flow periods in the summer of 1982. Relations among <span class="hlt">dissolved</span> oxygen, water discharge, biochemical oxygen demand, ammonia and nitrite plus nitrate <span class="hlt">concentrations</span>, and photosynthetic-oxygen production were simulated using a one-dimensional, steady-state computer model. Average <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> ranged from 8.0 milligrams per liter at the upstream end of the study reach at Decatur to 5.2 milligrams per liter 12.2 miles downstream. Ammonia <span class="hlt">concentrations</span> ranged from 45 milligrams per liter at the mouth of Stevens Creek (2.6 miles downstream from Decatur) to 0.03 milligram per liter at the downstream end of the study reach. Un-ionized ammonia <span class="hlt">concentrations</span> exceeded the maximum <span class="hlt">concentration</span> specified in the State water quality standard (0.04 milligram per liter) throughout most of the study reach. Model simulations indicated that oxidation of ammonia to form nitrite plus nitrate was the most significant process leading to low <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> in the river. (USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20040055394','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20040055394"><span>Structure and Dynamics of <span class="hlt">Freely</span> Suspended Liquid Crystals</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Clark, Noel A.</p> <p>2004-01-01</p> <p>Smectic liquid crystals are phases of rod shaped molecules organized into one dimensionally (1 D) periodic arrays of layers, each layer being between one and two molecular lengths thick. In the least ordered smectic phases, the smectics A and C, each layer is a two dimensional (2D) liquid. Additionally there are a variety of more ordered smectic phases having hexatic short range translational order or 2D crystalline or quasi long range translational order within the layers. The inherent fluid-layer structure and low vapor pressure of smectic liquid crystals enables the long term stabilization of <span class="hlt">freely</span> suspended, single component, layered fluid films as thin as 30A, a single molecular layer. The layering forces the films to be an integral number of smectic layers thick, quantizing their thickness in layer units and forcing a film of a particular number of layers to be physically homogeneous with respect to its layer structure over its entire area. Optical reflectivity enables the precise determination of the number of layers. These ultrathin <span class="hlt">freely</span> suspended liquid crystal films are structures of fundamental interest in condensed matter and fluid physics. They are the thinnest known stable fluid structures and have the largest surface-to-volume ratio of any stable fluid preparation, making them ideal for the study of the effects of reduced dimensionality on phase behavior and on fluctuation and interface phenomena. Their low vapor pressure and quantized thickness enable the effective use of microgravity to extend the study of basic capillary phenomena to ultrathin fluid films. <span class="hlt">Freely</span> suspended films have been a wellspring of new LC physics. They have been used to provide unique experimental conditions for the study of condensed phase transitions in two dimensions. They are the only system in which the hexatic has been unambiguously identified as a phase of matter, and the only physical system in which fluctuations of a 2D XY system and Kosterlitz Thouless phase</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18396373','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18396373"><span>Tertiary treatment of textile wastewater with combined media biological aerated filter (CMBAF) at different hydraulic loadings and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Fang; Zhao, Chao-Cheng; Zhao, Dong-Feng; Liu, Guo-Hua</p> <p>2008-12-15</p> <p>An up-flow biological aerated filter packed with two layers media was employed for tertiary treatment of textile wastewater secondary effluent. Under steady state conditions, good performance of the reactor was achieved and the average COD, NH(4)(+)-N and total nitrogen (TN) in the effluent were 31, 2 and 8mg/L, respectively. For a fixed <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span>, an increase of hydraulic loading resulted in a decrease in substrate removal. With the increase of hydraulic loadings from 0.13 to 0.78m(3)/(m(2)h), the removal efficiencies of COD, NH(4)(+)-N and TN all decreased, which dropped from 52 to 38%, from 90 to 68% and from 45 to 33%, respectively. In addition, the results also confirmed that the increase of COD and NH(4)(+)-N removal efficiencies resulted from the increase of DO <span class="hlt">concentrations</span>, but this variation trend was not observed for TN removal. With the increase of DO <span class="hlt">concentrations</span> from 2.4 to 6.1mg/L, the removal efficiencies of COD and NH(4)(+)-N were 39-53% and 64-88%, whenas TN removal efficiencies increased from 39 to 42% and then dropped to 35%.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26868162','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26868162"><span><span class="hlt">Dissolved</span> atmospheric gas in xylem sap measured with membrane inlet mass spectrometry.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Schenk, H Jochen; Espino, Susana; Visser, Ate; Esser, Bradley K</p> <p>2016-04-01</p> <p>A new method is described for measuring <span class="hlt">dissolved</span> gas <span class="hlt">concentrations</span> in small volumes of xylem sap using membrane inlet mass spectrometry. The technique can be used to determine <span class="hlt">concentrations</span> of atmospheric gases, such as argon, as reported here, or for any <span class="hlt">dissolved</span> gases and their isotopes for a variety of applications, such as rapid detection of trace gases from groundwater only hours after they were taken up by trees and rooting depth estimation. Atmospheric gas content in xylem sap directly affects the conditions and mechanisms that allow for gas removal from xylem embolisms, because gas can <span class="hlt">dissolve</span> into saturated or supersaturated sap only under gas pressure that is above atmospheric pressure. The method was tested for red trumpet vine, Distictis buccinatoria (Bignoniaceae), by measuring atmospheric gas <span class="hlt">concentrations</span> in sap collected at times of minimum and maximum daily temperature and during temperature increase and decline. Mean argon <span class="hlt">concentration</span> in xylem sap did not differ significantly from saturation levels for the temperature and pressure conditions at any time of collection, but more than 40% of all samples were supersaturated, especially during the warm parts of day. There was no significant diurnal pattern, due to high variability between samples. © 2015 John Wiley & Sons Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70174978','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70174978"><span>Biogeochemical controls of uranium bioavailability from the <span class="hlt">dissolved</span> phase in natural freshwaters</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Croteau, Marie-Noele; Fuller, Christopher C.; Cain, Daniel J.; Campbell, Kate M.; Aiken, George R.</p> <p>2016-01-01</p> <p>To gain insights into the risks associated with uranium (U) mining and processing, we investigated the biogeochemical controls of U bioavailability in the model freshwater speciesLymnaea stagnalis (Gastropoda). Bioavailability of <span class="hlt">dissolved</span> U(VI) was characterized in controlled laboratory experiments over a range of water hardness, pH, and in the presence of complexing ligands in the form of <span class="hlt">dissolved</span> natural organic matter (DOM). Results show that <span class="hlt">dissolved</span> U is bioavailable under all the geochemical conditions tested. Uranium uptake rates follow first order kinetics over a range encompassing most environmental <span class="hlt">concentrations</span>. Uranium uptake rates in L. stagnalis ultimately demonstrate saturation uptake kinetics when exposure <span class="hlt">concentrations</span> exceed 100 nM, suggesting uptake via a finite number of carriers or ion channels. The lack of a relationship between U uptake rate constants and Ca uptake rates suggest that U does not exclusively use Ca membrane transporters. In general, U bioavailability decreases with increasing pH, increasing Ca and Mg <span class="hlt">concentrations</span>, and when DOM is present. Competing ions did not affect U uptake rates. Speciation modeling that includes formation constants for U ternary complexes reveals that the aqueous <span class="hlt">concentration</span> of dicarbonato U species (UO2(CO3)2–2) best predicts U bioavailability to L. stagnalis, challenging the free-ion activity model postulate.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70027439','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70027439"><span>Relative effect of temperature and pH on diel cycling of <span class="hlt">dissolved</span> trace elements in prickly pear creek, Montana</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Jones, Clain A.; Nimick, D.A.; McCleskey, R. Blaine</p> <p>2004-01-01</p> <p>Diel (24 hr) cycles in <span class="hlt">dissolved</span> metal and As <span class="hlt">concentrations</span> have been documented in many northern Rocky Mountain streams in the U.S.A. The cause(s) of the cycles are unknown, although temperature- and pH-dependent sorption reactions have been cited as likely causes. A light/dark experiment was conducted to isolate temperature and pH as variables affecting diel metal cycles in Prickly Pear Creek, Montana. Light and dark chambers containing sediment and a strand of macrophyte were placed in the stream to simulate instream temperature oscillations. Photosynthesis-induced pH changes were allowed to proceed in the light chambers while photosynthesis was prevented in the dark chambers. Water samples were collected periodically for 22 hr in late July 2001 from all chambers and the stream. In the stream, <span class="hlt">dissolved</span> Zn <span class="hlt">concentrations</span> increased by 300% from late afternoon to early morning, while <span class="hlt">dissolved</span> As <span class="hlt">concentrations</span> exhibited the opposite pattern, increasing 33% between early morning and late afternoon. Zn and As <span class="hlt">concentrations</span> in the light chambers showed similar, though less pronounced, diel variations. Conversely, Zn and As <span class="hlt">concentrations</span> in the dark chambers had no obvious diel variation, indicating that light, or light-induced reactions, caused the variation. Temperature oscillations were nearly identical between light and dark chambers, strongly suggesting that temperature was not controlling the diel variations. As expected, pH was negatively correlated (P < 0.01) with <span class="hlt">dissolved</span> Zn <span class="hlt">concentrations</span> and positively correlated with <span class="hlt">dissolved</span> As <span class="hlt">concentrations</span> in both the light and dark chambers. From these experiments, photosynthesis-induced pH changes were determined to be the major cause of the diel <span class="hlt">dissolved</span> Zn and As cycles in Prickly Pear Creek. Further research is necessary in other streams to verify that this finding is consistent among streams having large differences in trace-element <span class="hlt">concentrations</span> and mineralogy of channel substrate. ?? 2004 Kluwer</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26ES..137a2046M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26ES..137a2046M"><span>Development of an aquaculture system using nanobubble technology for the optimation of <span class="hlt">dissolved</span> oxygen in culture media for nile tilapia (Oreochromis niloticus)</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Mahasri, G.; Saskia, A.; Apandi, P. S.; Dewi, N. N.; Rozi; Usuman, N. M.</p> <p>2018-04-01</p> <p>The purpose of this research was to discover the process of enrichment of <span class="hlt">dissolved</span> oxygen in fish cultivation media using nanobubble technology. This study was conducted with two treatments, namely a cultivation media without fish and a cultivation media containing 8 fish with an average body length of 24.5 cm. The results showed that the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen increased from 6.5 mg/L to 25 mg/L. The rate of increase in <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> for 30 minutes is 0.61 pp/minute. The rate of decrease in <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in treatment 1 is 3.08 ppm/day and in treatment 2 is 0.23 ppm/minute. It was concluded that nanobubble is able to increase <span class="hlt">dissolved</span> oxygen.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ACP....16.3185V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ACP....16.3185V"><span>Cloud water composition during HCCT-2010: Scavenging efficiencies, solute <span class="hlt">concentrations</span>, and droplet size dependence of inorganic ions and <span class="hlt">dissolved</span> organic carbon</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>van Pinxteren, Dominik; Wadinga Fomba, Khanneh; Mertes, Stephan; Müller, Konrad; Spindler, Gerald; Schneider, Johannes; Lee, Taehyoung; Collett, Jeffrey L.; Herrmann, Hartmut</p> <p>2016-03-01</p> <p>Cloud water samples were taken in September/October 2010 at Mt. Schmücke in a rural, forested area in Germany during the Lagrange-type Hill Cap Cloud Thuringia 2010 (HCCT-2010) cloud experiment. Besides bulk collectors, a three-stage and a five-stage collector were applied and samples were analysed for inorganic ions (SO42-,NO3-, NH4+, Cl-, Na+, Mg2+, Ca2+, K+), H2O2 (aq), S(IV), and <span class="hlt">dissolved</span> organic carbon (DOC). Campaign volume-weighted mean <span class="hlt">concentrations</span> were 191, 142, and 39 µmol L-1 for ammonium, nitrate, and sulfate respectively, between 4 and 27 µmol L-1 for minor ions, 5.4 µmol L-1 for H2O2 (aq), 1.9 µmol L-1 for S(IV), and 3.9 mgC L-1 for DOC. The <span class="hlt">concentrations</span> compare well to more recent European cloud water data from similar sites. On a mass basis, organic material (as DOC × 1.8) contributed 20-40 % (event means) to total solute <span class="hlt">concentrations</span> and was found to have non-negligible impact on cloud water acidity. Relative standard deviations of major ions were 60-66 % for solute <span class="hlt">concentrations</span> and 52-80 % for cloud water loadings (CWLs). The similar variability of solute <span class="hlt">concentrations</span> and CWLs together with the results of back-trajectory analysis and principal component analysis, suggests that <span class="hlt">concentrations</span> in incoming air masses (i.e. air mass history), rather than cloud liquid water content (LWC), were the main factor controlling bulk solute <span class="hlt">concentrations</span> for the cloud studied. Droplet effective radius was found to be a somewhat better predictor for cloud water total ionic content (TIC) than LWC, even though no single explanatory variable can fully describe TIC (or solute <span class="hlt">concentration</span>) variations in a simple functional relation due to the complex processes involved. Bulk <span class="hlt">concentrations</span> typically agreed within a factor of 2 with co-located measurements of residual particle <span class="hlt">concentrations</span> sampled by a counterflow virtual impactor (CVI) and analysed by an aerosol mass spectrometer (AMS), with the deviations being mainly caused by systematic</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015ACPD...1524311V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015ACPD...1524311V"><span>Cloud water composition during HCCT-2010: Scavenging efficiencies, solute <span class="hlt">concentrations</span>, and droplet size dependence of inorganic ions and <span class="hlt">dissolved</span> organic carbon</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>van Pinxteren, D.; Fomba, K. W.; Mertes, S.; Müller, K.; Spindler, G.; Schneider, J.; Lee, T.; Collett, J.; Herrmann, H.</p> <p>2015-09-01</p> <p>Cloud water samples were taken in September/October 2010 at Mt. Schmücke in a rural, forested area in Germany during the Lagrange-type Hill Cap Cloud Thuringia 2010 (HCCT-2010) cloud experiment. Besides bulk collectors, a 3-stage and a 5-stage collector were applied and samples were analysed for inorganic ions (SO42-, NO3-, NH4+, Cl-, Na+, Mg2+, Ca2+, K+), H2O2 (aq), S(IV), and <span class="hlt">dissolved</span> organic carbon (DOC). Campaign volume-weighted mean <span class="hlt">concentrations</span> were 191, 142, and 39 μmol L-1 for ammonium, nitrate, and sulfate, respectively, between 4 and 27 μmol L-1 for minor ions, 5.4 μmol L-1 for H2O2 (aq), 1.9 μmol L-1 for S(IV), and 3.9 mgC L-1 for DOC. The <span class="hlt">concentrations</span> compare well to more recent European cloud water data from similar sites. On a mass basis, organic material (as DOC · 1.8) contributed 20-40 % (event means) to total solute <span class="hlt">concentrations</span> and was found to have non-negligible impact on cloud water acidity. Relative standard deviations of major ions were 60-66 % for solute <span class="hlt">concentrations</span> and 52-80 % for cloud water loadings (CWLs). Contrary to some earlier suggestions, the similar variability of solute <span class="hlt">concentrations</span> and CWLs together with the results of back trajectory analysis and principal component analysis, suggests that <span class="hlt">concentrations</span> in incoming air masses (i.e. air mass history), rather than cloud liquid water content (LWC) was the main factor controlling bulk solute <span class="hlt">concentrations</span> at Mt. Schmücke. Droplet effective radius was found to be a somewhat better predictor for cloud water total ionic content (TIC) than LWC, even though no single explanatory variable can fully describe TIC (or solute <span class="hlt">concentration</span>) variations in a simple functional relation due to the complex processes involved. Bulk <span class="hlt">concentrations</span> typically agreed within a factor of 2 with co-located measurements of residual particle <span class="hlt">concentrations</span> sampled by a counterflow virtual impactor (CV) and analysed by an aerosol mass spectrometer (AMS), with the deviations being mainly</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMOS31D..08G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMOS31D..08G"><span>The Influence of Submarine Groundwater Discharge on Nearshore Marine <span class="hlt">Dissolved</span> Organic Carbon Reactivity, <span class="hlt">Concentration</span> Dynamics, and Offshore Export</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Goodridge, B.</p> <p>2017-12-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) is the largest pool of reduced carbon in the oceans, with a reservoir equivalent to atmospheric CO2. In nearshore marine regions, DOC sources include primary production, terrestrial DOC delivered by river discharge, and/or terrestrial and marine DOC delivered via submarine groundwater discharge (SGD). While the importance of SGD to coastal carbon cycling has been implicated, the actual influence of this process on nearshore carbon dynamics and offshore export has not been explicitly identified. This study, conducted at a predominantly marine-influenced intertidal beach-nearshore ocean system along the Santa Barbara, California coastline, aimed to address this knowledge gap. I coupled dark, temperature-controlled laboratory incubations, radioisotopic (Rn-222) SGD estimates, and a DOC box model to identify the influence of pore water mixing with seawater on nearshore DOC reactivity, <span class="hlt">concentration</span> dynamics, and offshore export. Even with a relatively low volumetric contribution, SGD pore water mixing altered nearshore DOC reactivity, and elevated the nearshore DOC <span class="hlt">concentration</span> by 0.9 to 5.6 µmol L-1 over nearshore seawater residence times ranging from 1 to 6 days. These elevated DOC <span class="hlt">concentrations</span> were equivalent to 1.2 to 7.5% of the mean offshore DOC <span class="hlt">concentration</span> taken during the summer months in the Santa Barbara Channel, when the coastal water column is highly thermally stratified. Despite the challenge of assessing carbon dynamics in physically and biogeochemically complex nearshore marine regions, this study demonstrates the need for future investigations to assess and account for SGD as a non-trivial component of coastal marine carbon cycles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009DSRI...56..166D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009DSRI...56..166D"><span><span class="hlt">Dissolved</span> DMSO production via biological and photochemical oxidation of <span class="hlt">dissolved</span> DMS in the Ross Sea, Antarctica</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>del Valle, Daniela A.; Kieber, David J.; Toole, Dierdre A.; Bisgrove, John; Kiene, Ronald P.</p> <p>2009-02-01</p> <p>Dimethylsulfoxide (DMSO) is an important degradation product of the climate-influencing gas dimethylsulfide (DMS). In the Ross Sea, Antarctica, <span class="hlt">dissolved</span> DMSO (DMSOd) <span class="hlt">concentrations</span> exhibited substantial seasonal and vertical variations. Surface water DMSOd <span class="hlt">concentrations</span> in pre-bloom waters were very low (<1 nM) but increased rapidly up to 41 nM during the spring Phaeocystis antarctica bloom (late November). Increases in DMSOd <span class="hlt">concentrations</span> lagged by several days increases in DMS <span class="hlt">concentrations</span>. Although DMSOd <span class="hlt">concentrations</span> reached relatively high levels during the spring bloom, <span class="hlt">concentrations</span> were generally higher (36.3-60.6 nM) during summer (January), even though phytoplankton biomass and DMS <span class="hlt">concentrations</span> had decreased by that time. During both seasons, DMSOd <span class="hlt">concentrations</span> were substantially higher within the surface mixed layer than below it. DMSOd production from biological DMS consumption (BDMSC) was higher during late November (3.4-5.2 nM d -1) than during the summer (0.7-2.4 nM d -1); therefore, production via BDMSC alone could not explain the higher DMSOd <span class="hlt">concentrations</span> encountered during the summer. Mixed layer-integrated DMSOd production from BDMSC was 2.5-13.7 times greater than production from <span class="hlt">dissolved</span> DMS photolysis during the P. antarctica bloom, while photolysis contributed 1.3 times more DMSO than BDMSC before the bloom. The DMSO yield from BDMSC was consistently higher within the upper mixed layer than at depths below. Experimental incubations with water from the mixed layer showed that exposure to full spectrum sunlight for 72 h caused an increase in the DMSO yield whereas exposure to only photosynthetically active radiation did not. This suggests that ultraviolet radiation is a potential factor shifting the fate of biologically consumed DMS toward DMSO. In general, the highest DMSO yields from BDMSC were in samples with slow biological DMS turnover, whereas fast turnover favored sulfate rather than DMSO as a major end-product. This study</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1999/4234/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1999/4234/report.pdf"><span>Characterization of water quality and simulation of temperature, nutrients, biochemical oxygen demand, and <span class="hlt">dissolved</span> oxygen in the Wateree River, South Carolina, 1996-98</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Feaster, Toby D.; Conrads, Paul</p> <p>2000-01-01</p> <p>In May 1996, the U.S. Geological Survey entered into a cooperative agreement with the Kershaw County Water and Sewer Authority to characterize and simulate the water quality in the Wateree River, South Carolina. Longitudinal profiling of <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> during the spring and summer of 1996 revealed <span class="hlt">dissolved</span>-oxygen minimums occurring upstream from the point-source discharges. The mean <span class="hlt">dissolved</span>-oxygen decrease upstream from the effluent discharges was 2.0 milligrams per liter, and the decrease downstream from the effluent discharges was 0.2 milligram per liter. Several theories were investigated to obtain an improved understanding of the <span class="hlt">dissolved</span>-oxygen dynamics in the upper Wateree River. Data suggest that the <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> decrease is associated with elevated levels of oxygen-consuming nutrients and metals that are flowing into the Wateree River from Lake Wateree. Analysis of long-term streamflow and water-quality data collected at two U.S. Geological Survey gaging stations suggests that no strong correlation exists between streamflow and <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> in the Wateree River. However, a strong negative correlation does exist between <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> and water temperature. Analysis of data from six South Carolina Department of Health and Environmental Control monitoring stations for 1980.95 revealed decreasing trends in ammonia nitrogen at all stations where data were available and decreasing trends in 5-day biochemical oxygen demand at three river stations. The influence of various hydrologic and point-source loading conditions on <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> in the Wateree River were determined by using results from water-quality simulations by the Branched Lagrangian Transport Model. The effects of five tributaries and four point-source discharges were included in the model. Data collected during two synoptic water-quality samplings on June 23.25 and August 11.13, 1997, were used to calibrate</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018BGeo...15.3345W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018BGeo...15.3345W"><span>Characteristics of wet <span class="hlt">dissolved</span> carbon deposition in a semi-arid catchment at the Loess Plateau, China</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, Linhua; Yen, Haw; Chen, Liding; E, Xinhui; Wang, Yafeng</p> <p>2018-06-01</p> <p>Wet <span class="hlt">dissolved</span> carbon deposition is a critical node of the global carbon cycle, but little is known about <span class="hlt">dissolved</span> organic and inorganic carbon (DOC and DIC) <span class="hlt">concentrations</span> and fluxes in the semi-arid areas of the Loess Plateau Region (LPR). In this study, we measured variations in DOC and DIC <span class="hlt">concentrations</span> in rainfalls at Yangjuangou Ecological Restoration and Soil and Water Observatory. Rainwater samples were collected in 16 rainfall events from July to September and the event-based, monthly <span class="hlt">concentrations</span> and fluxes of DOC and DIC were quantified. The results showed that the event-based <span class="hlt">concentrations</span> and fluxes of DOC and DIC were highly variable, ranging from 0.56 to 28.71 mg C L-1 and from 3.47 to 17.49 mg C L-1, respectively. The corresponding event-based fluxes ranged from 0.21-258.36 mg C m-2 and from 4.12 to 42.32 mg C m-2. The monthly <span class="hlt">concentrations</span> of DOC and DIC were 24.62 and 4.30 (July), 3.58 and 10.52 (August), and 1.01 and 5.89 (September) mg C L-1, respectively. Thus, the monthly deposition fluxes of DOC and DIC were 541.64/94.60, 131.03/385.03, and 44.44/259.16 mg C m-2 for July, August, and September, respectively. In addition, the <span class="hlt">concentrations</span> of DOC and DIC for the <span class="hlt">concentrated</span> rainfall season (July-September) in the studied catchment were 7.06 and 7.00 mg C L-1, respectively. The estimated annual wet <span class="hlt">dissolved</span> carbon depositions were 1.91 and 1.89 g C m-2 yr-1 for DOC and DIC, respectively. The results of this study suggest the variation in <span class="hlt">concentrations</span> and fluxes of DOC and DIC and explore that these variation may be related to the <span class="hlt">dissolved</span> carbon source and the rainfall characteristics during the <span class="hlt">concentrated</span> rainfall season in the semi-arid catchment of the LPR. Furthermore, these results also suggest that <span class="hlt">dissolved</span> carbon may be an important external input of carbon into terrestrial ecosystems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24701957','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24701957"><span>Nitritating-anammox biomass tolerant to high <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> and C/N ratio in treatment of yeast factory wastewater.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zekker, Ivar; Rikmann, Ergo; Tenno, Toomas; Seiman, Andrus; Loorits, Liis; Kroon, Kristel; Tomingas, Martin; Vabamäe, Priit; Tenno, Taavo</p> <p>2014-01-01</p> <p>Maintaining stability of low <span class="hlt">concentration</span> (< 1 g L(-1)) floccular biomass in the nitritation-anaerobic ammonium oxidation (anammox) process in the sequencing batch reactor (SBR) system for the treatment of high COD (> 15,000 mg O2 L(-1)) to N (1680 mg N L(-1)) ratio real wastewater streams coming from the food industry is challenging. The anammox process was suitable for the treatment of yeast factory wastewater containing relatively high and abruptly increased organic C/N ratio and <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentrations</span>. Maximum specific total inorganic nitrogen (TIN) loading and removal rates applied were 600 and 280 mg N g(-1) VSS d(-1), respectively. Average TIN removal efficiency over the operation period of 270 days was 70%. Prior to simultaneous reduction of high organics (total organic carbon > 600mg L(-1)) and N <span class="hlt">concentrations</span> > 400 mg L(-1), hydraulic retention time of 15 h and DO <span class="hlt">concentrations</span> of 3.18 (+/- 1.73) mg O2 L(-1) were applied. Surprisingly, higher DO <span class="hlt">concentrations</span> did not inhibit the anammox process efficiency demonstrating a wider application of cultivated anammox biomass. The SBR was fed rapidly over 5% of the cycle time at 50% volumetric exchange ratio. It maintained high free ammonia <span class="hlt">concentration</span>, suppressing growth of nitrite-oxidizing bacteria. Partial least squares and response surface modelling revealed two periods of SBR operation and the SBR performances change at different periods with different total nitrogen (TN) loadings. Anammox activity tests showed yeast factory-specific organic N compound-betaine and inorganic N simultaneous biodegradation. Among other microorganisms determined by pyrosequencing, anammox microorganism (uncultured Planctomycetales bacterium clone P4) was determined by polymerase chain reaction also after applying high TN loading rates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27525582','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27525582"><span>Impact of microbial physiology and microbial community structure on pharmaceutical fate driven by <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in nitrifying bioreactors.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stadler, Lauren B; Love, Nancy G</p> <p>2016-11-01</p> <p>Operation at low <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentrations</span> (<1 mg/L) in wastewater treatment could save utilities significantly by reducing aeration energy costs. However, few studies have evaluated the impact of low DO on pharmaceutical biotransformations during treatment. DO <span class="hlt">concentration</span> can impact pharmaceutical biotransformation rates during wastewater treatment both directly and indirectly: directly by acting as a limiting substrate that slows the activity of the microorganisms involved in biotransformation; and indirectly by shaping the microbial community and selecting for a community that performs pharmaceutical biotransformation faster (or slower). In this study, nitrifying bioreactors were operated at low (∼0.3 mg/L) and high (>4 mg/L) DO <span class="hlt">concentrations</span> to understand how DO growth conditions impacted microbial community structure. Short-term batch experiments using the biomass from the parent reactors were performed under low and high DO conditions to understand how DO <span class="hlt">concentration</span> impacts microbial physiology. Although the low DO parent biomass had a lower specific activity with respect to ammonia oxidation than the high DO parent reactor biomass, it had faster biotransformation rates of ibuprofen, sulfamethoxazole, 17α-ethinylestradiol, acetaminophen, and atenolol in high DO batch conditions. This was likely because the low DO reactor had a 2x higher biomass <span class="hlt">concentration</span>, was enriched for ammonia oxidizers (4x higher <span class="hlt">concentration</span>), and harbored a more diverse microbial community (3x more unique taxa) as compared to the high DO parent reactor. Overall, the results show that there can be indirect benefits from low DO operation over high DO operation that support pharmaceutical biotransformation during wastewater treatment. Copyright © 2016 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19730035840&hterms=salting&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dsalting','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19730035840&hterms=salting&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dsalting"><span>Thermodynamic properties of gases <span class="hlt">dissolved</span> in electrolyte solutions.</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Tiepel, E. W.; Gubbins, K. E.</p> <p>1973-01-01</p> <p>A method based on perturbation theory for mixtures is applied to the prediction of thermodynamic properties of gases <span class="hlt">dissolved</span> in electrolyte solutions. The theory is compared with experimental data for the dependence of the solute activity coefficient on <span class="hlt">concentration</span>, temperature, and pressure; calculations are included for partial molal enthalpy and volume of the <span class="hlt">dissolved</span> gas. The theory is also compared with previous theories for salt effects and found to be superior. The calculations are best for salting-out systems. The qualitative feature of salting-in is predicted by the theory, but quantitative predictions are not satisfactory for such systems; this is attributed to approximations made in evaluating the perturbation terms.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1424739-seiberg-witten-geometries-coulomb-branch-chiral-rings-which-freely-generated','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1424739-seiberg-witten-geometries-coulomb-branch-chiral-rings-which-freely-generated"><span>Seiberg-Witten geometries for Coulomb branch chiral rings which are not <span class="hlt">freely</span> generated</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Argyres, Philip C.; Lü, Yongchao; Martone, Mario</p> <p>2017-06-27</p> <p>Coulomb branch chiral rings of N = 2 SCFTs are conjectured to be <span class="hlt">freely</span> generated. While no counter-example is known, no direct evidence for the conjecture is known either. We initiate a systematic study of SCFTs with Coulomb branch chiral rings satisfying non-trivial relations, restricting our analysis to rank 1. The main result of our study is that (rank-1) SCFTs with non-<span class="hlt">freely</span> generated CB chiral rings when deformed by relevant deformations, always flow to theories with non-<span class="hlt">freely</span> generated CB rings. This implies that if they exist, they must thus form a distinct subset under RG flows. We also nd manymore » interesting characteristic properties that these putative theories satisfy which may be helpful in proving or disproving their existence using other methods.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://mo.water.usgs.gov/Reports/wrir03-4237-richards/','USGSPUBS'); return false;" href="http://mo.water.usgs.gov/Reports/wrir03-4237-richards/"><span>Simulation of hydrodynamics, temperature, and <span class="hlt">dissolved</span> oxygen in Table Rock Lake, Missouri, 1996-1997</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Green, W. Reed; Galloway, Joel M.; Richards, Joseph M.; Wesolowski, Edwin A.</p> <p>2003-01-01</p> <p>Outflow from Table Rock Lake and other White River reservoirs support a cold-water trout fishery of substantial economic yield in south-central Missouri and north-central Arkansas. The Missouri Department of Conservation has requested an increase in existing minimum flows through the Table Rock Lake Dam from the U.S. Army Corps of Engineers to increase the quality of fishable waters downstream in Lake Taneycomo. Information is needed to assess the effect of increased minimum flows on temperature and <span class="hlt">dissolved</span>- oxygen <span class="hlt">concentrations</span> of reservoir water and the outflow. A two-dimensional, laterally averaged, hydrodynamic, temperature, and <span class="hlt">dissolved</span>-oxygen model, CE-QUAL-W2, was developed and calibrated for Table Rock Lake, located in Missouri, north of the Arkansas-Missouri State line. The model simulates water-surface elevation, heat transport, and <span class="hlt">dissolved</span>-oxygen dynamics. The model was developed to assess the effects of proposed increases in minimum flow from about 4.4 cubic meters per second (the existing minimum flow) to 11.3 cubic meters per second (the increased minimum flow). Simulations included assessing the effect of (1) increased minimum flows and (2) increased minimum flows with increased water-surface elevations in Table Rock Lake, on outflow temperatures and <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span>. In both minimum flow scenarios, water temperature appeared to stay the same or increase slightly (less than 0.37 ?C) and <span class="hlt">dissolved</span> oxygen appeared to decrease slightly (less than 0.78 mg/L) in the outflow during the thermal stratification season. However, differences between the minimum flow scenarios for water temperature and <span class="hlt">dissolved</span>- oxygen <span class="hlt">concentration</span> and the calibrated model were similar to the differences between measured and simulated water-column profile values.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21508533','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21508533"><span>Labile, <span class="hlt">dissolved</span> and particulate PAHs and trace metals in wastewater: passive sampling, occurrence, partitioning in treatment plants.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gourlay-Francé, C; Bressy, A; Uher, E; Lorgeoux, C</p> <p>2011-01-01</p> <p>The occurrence and the partitioning of polycyclic aromatic hydrocarbons (PAHs) and seven metals (Al, Cd, Cr, Cu, Ni, Pb and Zn) were investigated in activated sludge wastewater treatment plants by means of passive and active sampling. <span class="hlt">Concentrations</span> total <span class="hlt">dissolved</span> and particulate contaminants were determined in wastewater at several points across the treatment system by means of grab sampling. Truly <span class="hlt">dissolved</span> PAHs were sampled by means of semipermeable membrane devices. Labile (inorganic and weakly complexed) <span class="hlt">dissolved</span> metals were also sampled using the diffusive gradient in thin film technique. This study confirms the robustness and the validity of these two passive sampling techniques in wastewater. All contaminant <span class="hlt">concentrations</span> decreased in wastewater along the treatment, although <span class="hlt">dissolved</span> and labile <span class="hlt">concentrations</span> sometimes increased for substances with less affinity with organic matter. Solid-liquid and <span class="hlt">dissolved</span> organic matter/water partitioning constants were estimated. The high variability of both partitioning constants for a simple substance and the poor relation between K(D) and K(OW) shows that the binding capacities of particles and organic matter are not uniform within the treatment and that other process than equilibrium sorption affect contaminant repartition and fate in wastewater.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018PhRvF...3d3801D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018PhRvF...3d3801D"><span>Self-sculpting of a <span class="hlt">dissolvable</span> body due to gravitational convection</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Davies Wykes, Megan S.; Huang, Jinzi Mac; Hajjar, George A.; Ristroph, Leif</p> <p>2018-04-01</p> <p>Natural sculpting processes such as erosion or dissolution often yield universal shapes that bear no imprint or memory of the initial conditions. Here we conduct laboratory experiments aimed at assessing the shape dynamics and role of memory for the simple case of a <span class="hlt">dissolvable</span> boundary immersed in a fluid. Though no external flow is imposed, dissolution and consequent density differences lead to gravitational convective flows that in turn strongly affect local <span class="hlt">dissolving</span> rates and shape changes, and we identify two distinct behaviors. A flat boundary <span class="hlt">dissolving</span> from its lower surface tends to retain its overall shape (an example of near perfect memory) while bearing small-scale pits that reflect complex near-body flows. A boundary <span class="hlt">dissolving</span> from its upper surface tends to erase its initial shape and form an upward spike structure that sharpens indefinitely. We propose an explanation for these different outcomes based on observations of the coupled shape dynamics, <span class="hlt">concentration</span> fields, and flows.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_17 --> <div id="page_18" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="341"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wsp/2358/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wsp/2358/report.pdf"><span>Characteristics and trends of streamflow and <span class="hlt">dissolved</span> solids in the upper Colorado River Basin, Arizona, Colorado, New Mexico, Utah, and Wyoming</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Liebermann, Timothy D.; Mueller, David K.; Kircher, James E.; Choquette, Anne F.</p> <p>1989-01-01</p> <p>Annual and monthly <span class="hlt">concentrations</span> and loads of <span class="hlt">dissolved</span> solids and major constituents were estimated for 70 streamflow-gaging stations in the Upper Colorado River Basin. Trends in streamflow, <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>, and <span class="hlt">dissolved</span>-solids loads were identified. Nonparametric trend-analysis techniques were used to determine step trends resulting from human activities upstream and long-term monotonic trends. Results were compared with physical characteristics of the basin and historical water-resource development in the basin to determine source areas of <span class="hlt">dissolved</span> solids and possible cause of trends. Mean annual <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> increases from less than 100 milligrams per liter in the headwater streams to more than 500 milligrams per liter in the outflow from the Upper Colorado River Basin. All the major tributaries that have high <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids are downstream from extensive areas of irrigated agriculture. However, irrigation predated the period of record for most sites and was not a factor in many identified trends. Significant annual trends were identified for 30 sites. Most of these trends were related to transbasin exports, changes in land use, salinity-control practices, or reservoir development. The primary factor affecting streamflow and <span class="hlt">dissolved</span>-solids <span class="hlt">concentration</span> and load has been the construction of large reservoirs. Reservoirs have decreased the seasonal and annual variability of streamflow and <span class="hlt">dissolved</span> solids in streams that drain the Gunnison and San Juan River basins. Fontenelle and Flaming Gorge Reservoirs have increased the <span class="hlt">dissolved</span>-solids load in the Green River because of dissolution of mineral salts from the bank material. The largest trends occurred downstream from Lake Powell. However, the period of record since the completion of filling was too short to estimate the long-term effects of that reservoir.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JIEIA.tmp..112P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JIEIA.tmp..112P"><span>Biodegradation of a Real Dye Wastewater Containing High <span class="hlt">Concentration</span> of Total <span class="hlt">Dissolved</span> Inorganic Salts (TDIS) in a Lab-Scale Activated Sludge Unit</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Patel, Upendra D.; Ruparelia, Jayesh; Patel, Margi</p> <p>2017-11-01</p> <p>Biodegradation studies on Dye wastewater (DW) are normally conducted on simulated wastewaters or aqueous dyes solutions supported by growth medium, and often, an easy carbon source such as glucose. This rarely resembles actual DW which is characterized by the presence of complex organic compounds, and a high <span class="hlt">concentration</span> of Total <span class="hlt">Dissolved</span> Inorganic Salts (TDIS). Biodegradation of real Direct Dyes Wastewater (DDW), and a mixed-waste stream (MWS) consisting of equal volumes of Direct and Acid dyes wastewaters, was carried out using a lab-scale activated sludge unit. The DDW and MWS had TDIS and COD <span class="hlt">concentrations</span> of 105 and 4.5 g/L, and 54 and 4.1 g/L, respectively. After acclimatization process of 70 days, 67% COD removal was achieved at influent TDIS and COD <span class="hlt">concentrations</span> of 79.6 g/L and 4320 mg/L, respectively, for the DDW at HRT of 3 days and MLVSS <span class="hlt">concentration</span> of 2000 mg/L. Although no sludge wastage was done, initially increased <span class="hlt">concentration</span> of MLVSS ( 2400 mg/L) decreased to 1700 mg/L with increase in TDIS. Using the biomass acclimatized for DDW for treatment of MWS, consistent COD removal of 70% was achieved at HRT of 4.3 days and an MLVSS <span class="hlt">concentration</span> of 1600 mg/L. Results suggest that significant COD removal can be achieved in real DW if biomass is gradually acclimatized to increasing TDIS <span class="hlt">concentrations</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25794043','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25794043"><span>How does predation affect the bioaccumulation of hydrophobic organic compounds in aquatic organisms?</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Xia, Xinghui; Li, Husheng; Yang, Zhifeng; Zhang, Xiaotian; Wang, Haotian</p> <p>2015-04-21</p> <p>It is well-known that the body burden of hydrophobic organic compounds (HOCs) increases with the trophic level of aquatic organisms. However, the mechanism of HOC biomagnification is not fully understood. To fill this gap, this study investigated the effect of predation on the bioaccumulation of polycyclic aromatic hydrocarbons (PAHs), one type of HOC, in low-to-high aquatic trophic levels under constant <span class="hlt">freely</span> <span class="hlt">dissolved</span> PAH <span class="hlt">concentrations</span> (1, 5, or 10 μg L(-1)) maintained by passive dosing systems. The tested PAHs included phenanthrene, anthracene, fluoranthene, and pyrene. The test organisms included zebrafish, which prey on Daphnia magna, and cichlids, which prey on zebrafish. The results revealed that for both zebrafish and cichlids, predation elevated the uptake and elimination rates of PAHs. The increase of uptake rate constant ranged from 20.8% to 39.4% in zebrafish with the amount of predation of 5 daphnids per fish per day, and the PAH uptake rate constant increased with the amount of predation. However, predation did not change the final bioaccumulation equilibrium; the equilibrium <span class="hlt">concentrations</span> of PAHs in fish only depended on the <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentration</span> in water. Furthermore, the lipid-normalized water-based bioaccumulation factor of each PAH was constant for fish at different trophic levels. These findings infer that the final bioaccumulation equilibrium of PAHs is related to a partition between water and lipids in aquatic organisms, and predation between trophic levels does not change bioaccumulation equilibrium but bioaccumulation kinetics at stable <span class="hlt">freely</span> <span class="hlt">dissolved</span> PAH <span class="hlt">concentrations</span>. This study suggests that if HOCs have not reached bioaccumulation equilibrium, biomagnification occurs due to enhanced uptake rates caused by predation in addition to higher lipid contents in higher trophic organisms. Otherwise, it is only due to the higher lipid contents in higher trophic organisms.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28453974','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28453974"><span>Influences of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> on biocathodic microbial communities in microbial fuel cells.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Rago, Laura; Cristiani, Pierangela; Villa, Federica; Zecchin, Sarah; Colombo, Alessandra; Cavalca, Lucia; Schievano, Andrea</p> <p>2017-08-01</p> <p><span class="hlt">Dissolved</span> oxygen (DO) at cathodic interface is a critical factor influencing microbial fuel cells (MFC) performance. In this work, three MFCs were operated with cathode under different DO conditions: i) air-breathing (A-MFC); ii) water-submerged (W-MFC) and iii) assisted by photosynthetic microorganisms (P-MFC). A plateau of maximum current was reached at 1.06±0.03mA, 1.48±0.06mA and 1.66±0.04mA, increasing respectively for W-MFC, P-MFC and A-MFC. Electrochemical and microbiological tools (Illumina sequencing, confocal microscopy and biofilm cryosectioning) were used to explore anodic and cathodic biofilm in each MFC type. In all cases, biocathodes improved oxygen reduction reaction (ORR) as compared to abiotic condition and A-MFC was the best performing system. Photosynthetic cultures in the cathodic chamber supplied high DO level, up to 16mg O2 L -1 , which sustained aerobic microbial community in P-MFC biocathode. Halomonas, Pseudomonas and other microaerophilic genera reached >50% of the total OTUs. The presence of sulfur reducing bacteria (Desulfuromonas) and purple non-sulfur bacteria in A-MFC biocathode suggested that the recirculation of sulfur compounds could shuttle electrons to sustain the reduction of oxygen as final electron acceptor. The low DO <span class="hlt">concentration</span> limited the cathode in W-MFC. A model of two different possible microbial mechanisms is proposed which can drive predominantly cathodic ORR. Copyright © 2017 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/203614-surface-microlayer-enrichment-polycyclic-aromatic-hydrocarbons-lower-chesapeake-bay','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/203614-surface-microlayer-enrichment-polycyclic-aromatic-hydrocarbons-lower-chesapeake-bay"><span>Surface microlayer enrichment of polycyclic aromatic hydrocarbons in lower Chesapeake Bay</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Liu, K.; Dickhut, R.M.</p> <p>1995-12-31</p> <p>Surface microlayer samples were collected with a rotating cylinder sampler in the York River and Elizabeth River tributaries of lower Chesapeake Bay every other month from May 1994 to June, 1995. Spatial and temporal variabilities were also investigated over an annual cycle as well as shorter periods (i.e. days). All the samples were analyzed for 17 polycyclic aromatic hydrocarbons, total suspended particulate matter (TSP), particular organic carbon (POC), total nitrogen(TN) and <span class="hlt">dissolved</span> organic carbon (DOC), and selected samples for chlorophyll. TSP in the surface microlayer was 10 to 100 times higher than that in the related bulk water. Particle associatedmore » PAH <span class="hlt">concentrations</span> were 20--50 times those in bulk surface water, whereas PAH <span class="hlt">concentrations</span> in <span class="hlt">freely</span> <span class="hlt">dissolved</span> phase of the surface microlayer were 5--60 times higher than <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> in the bulk water. Particulate PAH <span class="hlt">concentrations</span> increase with TSP in the surface microlayer and <span class="hlt">dissolved</span> PAH <span class="hlt">concentrations</span> increase with DOC. Overall, surface microlayer characteristics were found to be significantly affected by hydrological and meteorological parameters.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70029091','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70029091"><span>Differences in <span class="hlt">dissolved</span> cadmium and zinc uptake among stream insects: Mechanistic explanations</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Buchwalter, D.B.; Luoma, S.N.</p> <p>2005-01-01</p> <p>This study examined the extent to which <span class="hlt">dissolved</span> Cd and Zn uptake rates vary in several aquatic insect taxa commonly used as indicators of ecological health. We further attempted to explain the mechanisms underlying observed differences. By comparing <span class="hlt">dissolved</span> Cd and Zn uptake rates in several aquatic insect species, we demonstrated that species vary widely in these processes. <span class="hlt">Dissolved</span> uptake rates were not related to gross morphological features such as body size or gill size-features that influence water permeability and therefore have ionoregulatory importance. However, finer morphological features, specifically, the relative numbers of ionoregulatory cells (chloride cells), appeared to be related to <span class="hlt">dissolved</span> metal uptake rates. This observation was supported by Michaelis-Menten type kinetics experiments, which showed that <span class="hlt">dissolved</span> Cd uptake rates were driven by the numbers of Cd transporters and not by the affinities of those transporters to Cd. Calcium <span class="hlt">concentrations</span> in exposure media similarly affected Cd and Zn uptake rates in the caddisfly Hydropsyche californica. <span class="hlt">Dissolved</span> Cd and Zn uptake rates strongly co-varied among species, suggesting that these metals are transported by similar mechanisms.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26287211','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26287211"><span>Nano-Enriched and Autonomous Sensing Framework for <span class="hlt">Dissolved</span> Oxygen.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Shehata, Nader; Azab, Mohammed; Kandas, Ishac; Meehan, Kathleen</p> <p>2015-08-14</p> <p>This paper investigates a nano-enhanced wireless sensing framework for <span class="hlt">dissolved</span> oxygen (DO). The system integrates a nanosensor that employs cerium oxide (ceria) nanoparticles to monitor the <span class="hlt">concentration</span> of DO in aqueous media via optical fluorescence quenching. We propose a comprehensive sensing framework with the nanosensor equipped with a digital interface where the sensor output is digitized and dispatched wirelessly to a trustworthy data collection and analysis framework for consolidation and information extraction. The proposed system collects and processes the sensor readings to provide clear indications about the current or the anticipated <span class="hlt">dissolved</span> oxygen levels in the aqueous media.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26192081','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26192081"><span><span class="hlt">Dissolved</span> Organic Matter Quality in a Shallow Aquifer of Bangladesh: Implications for Arsenic Mobility.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mladenov, Natalie; Zheng, Yan; Simone, Bailey; Bilinski, Theresa M; McKnight, Diane M; Nemergut, Diana; Radloff, Kathleen A; Rahman, M Moshiur; Ahmed, Kazi Matin</p> <p>2015-09-15</p> <p>In some high arsenic (As) groundwater systems, correlations are observed between <span class="hlt">dissolved</span> organic matter (DOM) and As <span class="hlt">concentrations</span>, but in other systems, such relationships are absent. The role of labile DOM as the main driver of microbial reductive dissolution is not sufficient to explain the variation in DOM-As relationships. Other processes that may also influence As mobility include complexation of As by <span class="hlt">dissolved</span> humic substances, and competitive sorption and electron shuttling reactions mediated by humics. To evaluate such humic DOM influences, we characterized the optical properties of filtered surface water (n = 10) and groundwater (n = 24) samples spanning an age gradient in Araihazar, Bangladesh. Further, we analyzed large volume fulvic acid (FA) isolates (n = 6) for optical properties, C and N content, and (13)C NMR spectroscopic distribution. Old groundwater (>30 years old) contained primarily sediment-derived DOM and had significantly higher (p < 0.001) <span class="hlt">dissolved</span> As <span class="hlt">concentration</span> than groundwater that was younger than 5 years old. Younger groundwater had DOM spectroscopic signatures similar to surface water DOM and characteristic of a sewage pollution influence. Associations between <span class="hlt">dissolved</span> As, iron (Fe), and FA <span class="hlt">concentration</span> and fluorescence properties of isolated FA in this field study suggest that aromatic, terrestrially derived FAs promote As-Fe-FA complexation reactions that may enhance As mobility.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70012562','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70012562"><span>Azomethine H colorimetric method for determining <span class="hlt">dissolved</span> boron in water</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Spencer, R.R.; Erdmann, D.E.</p> <p>1979-01-01</p> <p>An automated colorimetric method for determining <span class="hlt">dissolved</span> boron in water is described. The boron is complexed with azomethine H, which is readily available as the condensation product of H acid (8-amino-1-naphthol-3,6-disulfonic acid) and salicylaldehyde. The absorbance of the yellow complex formed is then measured colorimetrically at 410 nm. Interference effects from other <span class="hlt">dissolved</span> species are minimized by the addition of diethylenetriaminepentaacetic acid (DTPA); however, iron, zinc, and bicarbonate interfere at <span class="hlt">concentrations</span> above 400 ??g/L, 2000 ??g/L, and 200 mg/L, respectively. The bicarbonate interference can be eliminated by careful acidification of the sample with <span class="hlt">concentrated</span> HCl to a pH between 5 and 6. Thirty samples per hour can be routinely analyzed over the range of from 10 to 400 ??g/L, boron.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5360494','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5360494"><span>Biocompatibility of “On-Command” <span class="hlt">Dissolvable</span> Tympanostomy Tube in the Rat Model</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Mai, Johnny P.; Dumont, Matthieu; Rossi, Christopher; Cleary, Kevin; Wiedermann, Joshua; Reilly, Brian K.</p> <p>2016-01-01</p> <p>Objectives/Hypothesis A prototype tympanostomy tube, composed of (polybutyl/methyl methacrylate-co-dimethyl amino ethyl methacrylate (PBM)), was tested to (1) evaluate the effect of PBM tubes on rat dermis as a corollary for biocompatibility and (2) to observe the efficacy of dissolution with isopropyl alcohol (iPrOH) and ethanol (EtOH). Subjects and Methods A two-part study was conducted to assess biocompatible substance with inducible <span class="hlt">dissolvability</span> as a critical characteristic for a newly engineered tympanostomy tube. First, tympanostomy tubes were inserted subcutaneously in 10 rats, which served as an animal model for biosafety and compared to traditional tubes with respect to histologic reaction. Tissue surrounding the PBM prototype tubes was submitted for histopathology and demonstrated no tissue reactivity or signs of major inflammation. In the second part, we evaluated the <span class="hlt">dissolvability</span> of the tube with either isopropyl alcohol, ethanol, ofloxacin, ciprodex, water, and soapy water. PBM tubes were exposed to decreasing <span class="hlt">concentrations</span> of iPrOH and EtOH with interval qualitative assessment of dissolution. Results (1) Histologic examination did not reveal pathology with PBM tubes; (2) <span class="hlt">Concentrations</span> of at least 50% iPrOH and EtOH <span class="hlt">dissolve</span> PBM tubes within 48 hours while <span class="hlt">concentrations</span> of at least 75% iPrOH and EtOH were required for dissolution when exposure was limited to four 20-minute intervals. Conclusion PBM is biocompatible in the rat model. Additionally, PBM demonstrates rapid dissolution upon alcohol-based stimuli, validating the proof-of-concept of <span class="hlt">dissolvable</span> “on-command” or biocommandible ear tubes. Further testing of PBM is needed with a less ototoxic <span class="hlt">dissolver</span> and in a better simulated middle ear environment, before testing can be performed in humans. PMID:27796039</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014EGUGA..16.8558W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014EGUGA..16.8558W"><span>Greenhouse gases <span class="hlt">dissolved</span> in soil solution - often ignored, but important?</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Weymann, Daniel; Brueggemann, Nicolas; Puetz, Thomas; Vereecken, Harry</p> <p>2014-05-01</p> <p>Flux measurements of climate-relevant trace gases from soils are frequently undertaken in contemporary ecosystem studies and substantially contribute to our understanding of greenhouse gas balances of the biosphere. While the great majority of such investigations builds on closed chamber and eddy covariance measurements, where upward gas fluxes to the atmosphere are measured, fewest concurrently consider greenhouse gas dissolution in the seepage and leaching of <span class="hlt">dissolved</span> gases via the vadose zone to the groundwater. Here we present annual leaching losses of <span class="hlt">dissolved</span> N2O and CO2 from arable, grassland, and forest lysimeter soils from three sites differing in altitude and climate. We aim to assess their importance in comparison to direct N2O emission, soil respiration, and further leaching parameters of the C- and N cycle. The lysimeters are part of the Germany-wide lysimeter network initiative TERENO-SoilCan, which investigates feedbacks of climate change to the pedosphere on a long-term scale. Soil water samples were collected weekly from different depths of the profiles by means of suction cups. A laboratory pre-experiment proved that no degassing occurred under those sampling conditions. We applied the headspace equilibration technique to determine <span class="hlt">dissolved</span> gas <span class="hlt">concentrations</span> by gas chromatography. The seepage water of all lysimeters was consistently supersaturated with N2O and CO2 compared to water equilibrated ambient air. In terms of N2O, leaching losses increased in the ascending order forest, grassland, and arable soils, respectively. In case of the latter soils, we observed a strong variability of N2O, with <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> up to 23 μg N L-1. However, since seepage discharge of the arable lysimeters was comparatively small and mostly limited to the hydrological winter season, leached N2O appeared to be less important than direct N2O emissions. In terms of <span class="hlt">dissolved</span> CO2,our measurements revealed considerable leaching losses from the mountainous</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24434701','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24434701"><span>Recovering/<span class="hlt">concentrating</span> of hemicellulosic sugars and acetic acid by nanofiltration and reverse osmosis from prehydrolysis liquor of kraft based hardwood <span class="hlt">dissolving</span> pulp process.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ahsan, Laboni; Jahan, M Sarwar; Ni, Yonghao</p> <p>2014-03-01</p> <p>This work investigated the feasibility of recovering and <span class="hlt">concentrating</span> sugars and acetic acid (HAc) from prehydrolysis liquor (PHL) of the kraft-based <span class="hlt">dissolving</span> pulp process prior to fermentation of hemicellulosic sugars, by the combination of activated carbon adsorption, nanofiltration (NF) and reverse osmosis (RO) processes. To reduce the fouling PHL was subjected to adsorption on activated carbon, then the treated PHL (TPHL) passed through a nanofiltration (NF DK) membrane to retain the sugars, and the permeate of acetic acid rich solution was passed through a reverse osmosis membrane (RO SG). It was found that for NF process sugars were <span class="hlt">concentrated</span> from 48 to 227g/L at a volume reduction factor (VRF) of 5 while 80 to 90% of acetic acid was permeated. For the reverse osmosis process, 68% of acetic acid retention was achieved at pH 4.3 and 500 psi pressure and the HAc <span class="hlt">concentration</span> increased from 10 to 50g/L. Crown Copyright © 2013. Published by Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.V11A0324C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.V11A0324C"><span>Geochemistry of High Temperature Vent Fluids in Yellowstone Lake: <span class="hlt">Dissolved</span> Carbon and Sulfur <span class="hlt">Concentrations</span> and Isotopic Data</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cino, C.; Seyfried, W. E., Jr.; Tan, C.; Fu, Q.</p> <p>2017-12-01</p> <p> for subaerial vents. The cause of these measured high <span class="hlt">dissolved</span> H2S <span class="hlt">concentrations</span> in Yellowstone Lake may result from temperature and/or redox effects.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70028311','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70028311"><span>Response of oxidative enzyme activities to nitrogen deposition affects soil <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Waldrop, M.P.; Zak, D.R.</p> <p>2006-01-01</p> <p>Recent evidence suggests that atmospheric nitrate (NO3- ) deposition can alter soil carbon (C) storage by directly affecting the activity of lignin-degrading soil fungi. In a laboratory experiment, we studied the direct influence of increasing soil NO 3- <span class="hlt">concentration</span> on microbial C cycling in three different ecosystems: black oak-white oak (BOWO), sugar maple-red oak (SMRO), and sugar maple-basswood (SMBW). These ecosystems span a broad range of litter biochemistry and recalcitrance; the BOWO ecosystem contains the highest litter lignin content, SMRO had intermediate lignin content, and SMBW leaf litter has the lowest lignin content. We hypothesized that increasing soil solution NO 3- would reduce lignolytic activity in the BOWO ecosystem, due to a high abundance of white-rot fungi and lignin-rich leaf litter. Due to the low lignin content of litter in the SMBW, we further reasoned that the NO3- repression of lignolytic activity would be less dramatic due to a lower relative abundance of white-rot basidiomycetes; the response in the SMRO ecosystem should be intermediate. We increased soil solution NO3- <span class="hlt">concentrations</span> in a 73-day laboratory incubation and measured microbial respiration and soil solution <span class="hlt">dissolved</span> organic carbon (DOC) and phenolics <span class="hlt">concentrations</span>. At the end of the incubation, we measured the activity of ??-glucosidase, N-acetyl-glucosaminidase, phenol oxidase, and peroxidase, which are extracellular enzymes involved with cellulose and lignin degradation. We quantified the fungal biomass, and we also used fungal ribosomal intergenic spacer analysis (RISA) to gain insight into fungal community composition. In the BOWO ecosystem, increasing NO 3- significantly decreased oxidative enzyme activities (-30% to -54%) and increased DOC (+32% upper limit) and phenolic (+77% upper limit) <span class="hlt">concentrations</span>. In the SMRO ecosystem, we observed a significant decrease in phenol oxidase activity (-73% lower limit) and an increase in soluble phenolic <span class="hlt">concentrations</span></p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28281760','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28281760"><span>Modeling Closed Equilibrium Systems of H2O-<span class="hlt">Dissolved</span> CO2-Solid CaCO3.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Tenno, Toomas; Uiga, Kalev; Mashirin, Alexsey; Zekker, Ivar; Rikmann, Ergo</p> <p>2017-04-27</p> <p>In many places in the world, including North Estonia, the bedrock is limestone, which consists mainly of CaCO 3 . Equilibrium processes in water involving <span class="hlt">dissolved</span> CO 2 and solid CaCO 3 play a vital role in many biological and technological systems. The solubility of CaCO 3 in water is relatively low. Depending on the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> CO 2 , the solubility of CaCO 3 changes, which determines several important ground- and wastewater parameters, for example, Ca 2+ <span class="hlt">concentration</span> and pH. The distribution of ions and molecules in the closed system solid H 2 O-<span class="hlt">dissolved</span> CO 2 -solid CaCO 3 is described in terms of a structural scheme. Mathematical models were developed for the calculation of pH and <span class="hlt">concentrations</span> of ions and molecules (Ca 2+ , CO 3 2- , HCO 3 - , H 2 CO 3 , CO 2 , H + , and OH - ) in the closed equilibrium system at different initial <span class="hlt">concentrations</span> of CO 2 in the water phase using an iteration method. The developed models were then experimentally validated.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27474282','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27474282"><span>Monitoring <span class="hlt">dissolved</span> orthophosphate in a struvite precipitation reactor with a voltammetric electronic tongue.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Aguado, Daniel; Barat, Ramón; Soto, Juan; Martínez-Mañez, Ramón</p> <p>2016-10-01</p> <p>This study demonstrates the feasibility of using a voltammetric electronic tongue to monitor effluent <span class="hlt">dissolved</span> orthophosphate <span class="hlt">concentration</span> in a struvite precipitation reactor. The electrochemical response of the electronic tongue to the presence of orthophosphate in samples collected from the effluent of the precipitation reactor is used to predict orthophosphate <span class="hlt">concentration</span> via a statistical model based on Partial Least Squares (PLS) Regression. PLS predictions were suitable for this monitoring application in which precipitation efficiencies higher than 80% (i.e., effluent <span class="hlt">dissolved</span> orthophosphate <span class="hlt">concentrations</span> lower than 40mg P-PO4(3-) L(-1)) could be considered as indicator of good process performance. The electronic tongue consisted of a set of metallic (noble and non-noble) electrodes housed inside a stainless steel cylinder which was used as the body of the electronic tongue system. Fouling problems were prevented via a simple mechanical polishing of the electrodes. The measurement of each sample with the electronic tongue was done in less than 3s. Conductivity of the samples only affected the electronic tongue marginally, being the main electrochemical response due to the orthophosphate <span class="hlt">concentration</span> in the samples. Copper, silver, iridium and rhodium were the electrodes that exhibited noticeable response correlated with the <span class="hlt">dissolved</span> orthophosphate <span class="hlt">concentration</span> variations, while gold, platinum and especially cobalt and nickel were the less useful electrodes for this application. Copyright © 2016 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29486435','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29486435"><span>Influence of land cover on riverine <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> and export in the Three Rivers Headwater Region of the Qinghai-Tibetan Plateau.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ma, Xiaoliang; Liu, Guimin; Wu, Xiaodong; Smoak, Joseph M; Ye, Linlin; Xu, Haiyan; Zhao, Lin; Ding, Yongjian</p> <p>2018-07-15</p> <p>The Qinghai-Tibetan plateau (QTP) stores a large amount of soil organic carbon and is the headwater region for several large rivers in Asia. Therefore, it is important to understand the influence of environmental factors on river water quality and the <span class="hlt">dissolved</span> organic carbon (DOC) export in this region. We examined the water physico-chemical characteristics, DOC <span class="hlt">concentrations</span> and export rates of 7 rivers under typical land cover types in the Three Rivers Headwater Region during August 2016. The results showed that the highest DOC <span class="hlt">concentrations</span> were recorded in the rivers within the catchment of alpine wet meadow and meadow. These same rivers had the lowest total suspended solids (TSS) <span class="hlt">concentrations</span>. The rivers within steppe and desert had the lowest DOC <span class="hlt">concentrations</span> and highest TSS <span class="hlt">concentrations</span>. The discharge rates and catchment areas were negatively correlated with DOC <span class="hlt">concentrations</span>. The SUVA 254 values were significantly negatively correlated with DOC <span class="hlt">concentrations</span>. The results suggest that the vegetation degradation, which may represent permafrost degradation, can lead to a decrease in DOC <span class="hlt">concentration</span>, but increasing DOC export and soil erosion. In addition, some of the exported DOC will rapidly decompose in the river, and therefore affect the regional carbon cycle, as well as the water quality in the source water of many large Asian rivers. Copyright © 2018 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017MS%26E..209a2110M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017MS%26E..209a2110M"><span>Highly Polluted Wastewaters Treatment by Improved <span class="hlt">Dissolved</span> Air Flotation Technology</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Moga, I. C.; Covaliu, C. I.; Matache, M. G.; Doroftei, B. I.</p> <p>2017-06-01</p> <p>Numerous investigations are oriented towards the development of new wastewater treatment technologies, having high efficiencies for removing even low <span class="hlt">concentrations</span> of pollutants found in water. These efforts were determined by the destroyer impact of the pollutants to the environment and human’s health. For this reason this paper presents our study concerning an improved <span class="hlt">dissolved</span> air flotation technology for wastewater treatment. There is described a <span class="hlt">dissolved</span> air flotation (DAF) installation composed by two equipments: pressurized capsule and lamellar settling. Also, there are presented some advantages of using nanoparticles as flotation collectors.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016APS..MAR.P9015P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016APS..MAR.P9015P"><span><span class="hlt">Freely</span>-tunable broadband polarization rotator for terahertz waves</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Peng, Ru-Wen; Fan, Ren-Hao; Zhou, Yu; Jiang, Shang-Chi; Xiong, Xiang; Huang, Xian-Rong; Wang, Mu</p> <p></p> <p>It is known that commercially-available terahertz (THz) emitters usually generate linearly polarized waves only along certain directions, but in practice, a polarization rotator that is capable of rotating the polarization of THz waves to any direction is particularly desirable and it will have various important applications. In this work, we demonstrate a <span class="hlt">freely</span> tunable polarization rotator for broadband THz waves using a three-rotating-layer metallic grating structure, which can conveniently rotate the polarization of a linearly polarized THz wave to any desired direction with nearly perfect conversion efficiency. The device performance has been experimentally demonstrated by both THz transmission spectra and direct imaging. The polarization rotation originates from multi wave interference in the three-layer grating structure based on the scattering-matrix analysis. We can expect that this active broadband polarization rotator has wide applications in analytical chemistry, biology, communication technology, imaging, etc.. Reference: R. H. Fan, Y. Zhou, X. P. Ren, R. W. Peng, S. C. Jiang, D. H. Xu, X. Xiong, X. R. Huang, and Mu Wang, Advanced Materials 27,1201(2015). <span class="hlt">Freely</span>-tunable broadband polarization rotator for terahertz waves.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016APS..MARS36011S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016APS..MARS36011S"><span>Visualizing Nanoscopic Topography and Patterns in <span class="hlt">Freely</span> Standing Thin Films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sharma, Vivek; Zhang, Yiran; Yilixiati, Subinuer</p> <p></p> <p>Thin liquid films containing micelles, nanoparticles, polyelectrolyte-surfactant complexes and smectic liquid crystals undergo thinning in a discontinuous, step-wise fashion. The discontinuous jumps in thickness are often characterized by quantifying changes in the intensity of reflected monochromatic light, modulated by thin film interference from a region of interest. Stratifying thin films exhibit a mosaic pattern in reflected white light microscopy, attributed to the coexistence of domains with various thicknesses, separated by steps. Using Interferometry Digital Imaging Optical Microscopy (IDIOM) protocols developed in the course of this study, we spatially resolve for the first time, the landscape of stratifying <span class="hlt">freely</span> standing thin films. We distinguish nanoscopic rims, mesas and craters, and follow their emergence and growth. In particular, for thin films containing micelles of sodium dodecyl sulfate (SDS), these topological features involve discontinuous, thickness transitions with <span class="hlt">concentration</span>-dependent steps of 5-25 nm. These non-flat features result from oscillatory, periodic, supramolecular structural forces that arise in confined fluids, and arise due to complex coupling of hydrodynamic and thermodynamic effects at the nanoscale.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_18 --> <div id="page_19" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="361"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18306801','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18306801"><span>[Determination of chromphoric <span class="hlt">dissolved</span> organic matter in water from different sources].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Xian-ping; Li, Lei; Dai, Jin-feng; Wang, Xiao-ru; Lee, Frank S C</p> <p>2007-10-01</p> <p>Chromophoric <span class="hlt">dissolved</span> organic matter (CDOM) represents the fraction of the <span class="hlt">dissolved</span> organic pool which absorbs light in the visible as well as UV ranges. It could affect the color of the waters. It is necessary to study it during in research on ecosystem, remote sensing of the water color and the cycle of carbon in waters. CDOM can fluoresce when excited, so fluorescence spectrum has been used to study its origin, distribution, and change. In the present article the fluorescence spectrophotometer was used to study the relation between the fluorescence intensity, spectrum area and the <span class="hlt">concentration</span> of CDOM. When the <span class="hlt">concentration</span> of CDOM is low (less than 75 mg x L(-1)), there is a better linear relationship (r2 > 0.98) between the fluorescence intensity, the spectrum area and the <span class="hlt">concentration</span> of CDOM. Meanwhile good linear relations were found between the fluorescence intensity and spectrum area, which showed the same changeable trend of the fluorescence intensity and spectrum area with the <span class="hlt">concentration</span> change of CDOM. A method was established to quantify the <span class="hlt">concentration</span> of CDOM in water from different source using the linear relationship between the spectrum area and the <span class="hlt">concentration</span>. It suits the complicated constituent analysis of CDOM and could really and accurately show the <span class="hlt">concentration</span> of CDOM in natural water.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17824538','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17824538"><span>Simultaneous nitrification, denitrification, and phosphorus removal in single-tank low-<span class="hlt">dissolved</span>-oxygen systems under cyclic aeration.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ju, Lu-Kwang; Huang, Lin; Trivedi, Hiren</p> <p>2007-08-01</p> <p>Simultaneous nitrification and denitrification (SND or SNdN) may occur at low <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>. In this study, bench-scale (approximately 6 L) bioreactors treating a continuous feed of synthetic wastewater were used to evaluate the effects of solids retention time and low <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span>, under cyclic aeration, on the removal of organics, nitrogen, and phosphorus. The cyclic aeration was carried out with repeated cycles of 1 hour at a higher <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (HDO) and 30 minutes at a lower (or zero) <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (LDO). Compared with aeration at constant <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>, the cyclic aeration, when operated with proper combinations of HDO and LDO, produced better-settling sludge and more complete nitrogen and phosphorus removal. For nitrogen removal, the advantage resulted from the more readily available nitrate and nitrite (generated by nitrification during the HDO period) for denitrification (during the LDO period). For phosphorus removal, the advantage of cyclic aeration came from the development of a higher population of polyphosphate-accumulating organisms, as indicated by the higher phosphorus contents in the sludge solids of the cyclically aerated systems. Nitrite shunt was also observed to occur in the LDO systems. Higher ratios of nitrite to nitrate were found in the systems of lower HDO (and, to less dependency, higher LDO), suggesting that the nitrite shunt took place mainly because of the disrupted nitrification at lower HDO. The study results indicated that the HDO used should be kept reasonably high (approximately 0.8 mg/L) or the HDO period prolonged, to promote adequate nitrification, and the LDO kept low (< or =0.2 mg/L), to achieve more complete denitrification and higher phosphorus removal. The above findings in the laboratory systems find strong support from the results obtained in full-scale plant implementation. Two plant case studies using the cyclic low-<span class="hlt">dissolved</span></p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2001JGR...106.2517K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2001JGR...106.2517K"><span>Seasonal and nonseasonal variability of satellite-derived chlorophyll and colored <span class="hlt">dissolved</span> organic matter <span class="hlt">concentration</span> in the California Current</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kahru, Mati; Mitchell, B. Greg</p> <p>2001-02-01</p> <p>Time series of surface chlorophyll a <span class="hlt">concentration</span> (Chl) and colored <span class="hlt">dissolved</span> organic matter (CDOM) derived from the Ocean Color and Temperature Sensor and Sea-Viewing Wide Field-of-View Sensor were evaluated for the California Current area using regional algorithms. Satellite data composited for 8-day periods provide the ability to describe large-scale changes in surface parameters. These changes are difficult to detect based on in situ observations alone that suffer from undersampling the large temporal and spatial variability, especially in Chl. We detected no significant bias in satellite Chl estimates compared with ship-based measurements. The variability in CDOM <span class="hlt">concentration</span> was significantly smaller than that in Chl, both spatially and temporally. While being subject to large interannual and short-term variations, offshore waters (100-1000 km from the shore) have an annual cycle of Chl and CDOM with a maximum in winter-spring (December-March) and a minimum in late summer. For inshore waters the maximum is more likely in spring (April-May). We detect significant increase in both Chl and CDOM off central and southern California during the La Niña year of 1999. The trend of increasing Chl and CDOM from October 1996 to June 2000 is statistically significant in many areas.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25971808','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25971808"><span>Characteristics and source identification of <span class="hlt">dissolved</span> trace elements in the Jinshui River of the South Qinling Mts., China.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bu, Hongmei; Wang, Weibo; Song, Xianfang; Zhang, Quanfa</p> <p>2015-09-01</p> <p><span class="hlt">Dissolved</span> trace elements and physiochemical parameters were analyzed to investigate their physicochemical characteristics and identify their sources at 12 sampling sites of the Jinshui River in the South Qinling Mts., China from October 2006 to November 2008. The two-factor ANOVA indicated significant temporal variations of the <span class="hlt">dissolved</span> Cu, Fe, Sr, Si, and V (p < 0.001 or p < 0.05). With the exception of Sr (p < 0.001), no significant spatial variations were found. Distributions and <span class="hlt">concentrations</span> of the <span class="hlt">dissolved</span> trace elements displayed that <span class="hlt">dissolved</span> Cu, Fe, Sr, Si, V, and Cr were originated from chemical weathering and leaching from the soil and bedrock. <span class="hlt">Dissolved</span> Cu, Fe, Sr, As, and Si were also from anthropogenic inputs (farming and domestic effluents). Correlation and regression analysis showed that the chemical and physical processes of <span class="hlt">dissolved</span> Cu was influenced by water temperature and <span class="hlt">dissolved</span> oxygen (DO) to some degree. <span class="hlt">Dissolved</span> Fe and Sr were affected by colloid destabilization or sedimentary inputs. <span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> Si were slightly controlled by biological uptake. Principal component analysis confirmed that Fe, Sr, and V resulted from domestic effluents, agricultural runoff, and confluence, whereas As, Cu, and Si were from agricultural activities, and Cr and Zn through natural processes. The research results provide a reference for ecological restoration and protection of the river environment in the Qinling Mts., China.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70170058','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70170058"><span>Changes between early development (1930–60) and recent (2005–15) groundwater-level altitudes and <span class="hlt">dissolved</span>-solids and nitrate <span class="hlt">concentrations</span> In and near Gaines, Terry, and Yoakum Counties, Texas</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Thomas, Jonathan V.; Teeple, Andrew; Payne, Jason; Ikard, Scott</p> <p>2016-06-21</p> <p>During the recent period, median <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> of less than 1,000 milligrams per liter (mg/L) were predominantly measured in the western part of the study area, and median <span class="hlt">concentrations</span> of more than 1,000 mg/L were predominantly measured in the eastern part of the study area. A general pattern of increasing nitrate <span class="hlt">concentrations</span> from west to the northeast was evident in the study area. Nitrate <span class="hlt">concentrations</span> measured in samples collected from 16 wells completed in the Ogallala aquifer for the recent period were equal to or greater than 10 mg/L, the primary drinking water standard for finished drinking water.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://pubs.water.usgs.gov/wri034092/','USGSPUBS'); return false;" href="http://pubs.water.usgs.gov/wri034092/"><span>Simulation of Temperature, Nutrients, Biochemical Oxygen Demand, and <span class="hlt">Dissolved</span> Oxygen in the Catawba River, South Carolina, 1996-97</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Feaster, Toby D.; Conrads, Paul; Guimaraes, Wladmir B.; Sanders, Curtis L.; Bales, Jerad D.</p> <p>2003-01-01</p> <p>Time-series plots of <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> were determined for various simulated hydrologic and point-source loading conditions along a free-flowing section of the Catawba River from Lake Wylie Dam to the headwaters of Fishing Creek Reservoir in South Carolina. The U.S. Geological Survey one-dimensional dynamic-flow model, BRANCH, was used to simulate hydrodynamic data for the Branched Lagrangian Transport Model. Waterquality data were used to calibrate the Branched Lagrangian Transport Model and included <span class="hlt">concentrations</span> of nutrients, chlorophyll a, and biochemical oxygen demand in water samples collected during two synoptic sampling surveys at 10 sites along the main stem of the Catawba River and at 3 tributaries; and continuous water temperature and <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> measured at 5 locations along the main stem of the Catawba River. A sensitivity analysis of the simulated <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> to model coefficients and data inputs indicated that the simulated <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> were most sensitive to watertemperature boundary data due to the effect of temperature on reaction kinetics and the solubility of <span class="hlt">dissolved</span> oxygen. Of the model coefficients, the simulated <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> was most sensitive to the biological oxidation rate of nitrite to nitrate. To demonstrate the utility of the Branched Lagrangian Transport Model for the Catawba River, the model was used to simulate several water-quality scenarios to evaluate the effect on the 24-hour mean <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> at selected sites for August 24, 1996, as simulated during the model calibration period of August 23 27, 1996. The first scenario included three loading conditions of the major effluent discharges along the main stem of the Catawba River (1) current load (as sampled in August 1996); (2) no load (all point-source loads were removed from the main stem of the Catawba River; loads from the main tributaries were not removed); and (3</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1373545','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1373545"><span>Analysis of maximum allowable fragment heights during dissolution of high flux isotope reactor fuel in an h-canyon <span class="hlt">dissolver</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Daniel, G.; Rudisill, T.</p> <p>2017-07-17</p> <p>As part of the Spent Nuclear Fuel (SNF) processing campaign, H-Canyon is planning to begin <span class="hlt">dissolving</span> High Flux Isotope Reactor (HFIR) fuel in late FY17 or early FY18. Each HFIR fuel core contains inner and outer fuel elements which were fabricated from uranium oxide (U 3O 8) dispersed in a continuous Al phase using traditional powder metallurgy techniques. Fuels fabricated in this manner, like other SNF’s processed in H-Canyon, <span class="hlt">dissolve</span> by the same general mechanisms with similar gas generation rates and the production of H 2. The HFIR fuel cores will be <span class="hlt">dissolved</span> using a flowsheet developed by the Savannahmore » River National Laboratory (SRNL) in either the 6.4D or 6.1D <span class="hlt">dissolver</span> using a unique insert. Multiple cores will be charged to the same <span class="hlt">dissolver</span> solution maximizing the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> Al. The recovered U will be down-blended into low-enriched U for subsequent use as commercial reactor fuel. During the development of the HFIR fuel dissolution flowsheet, the cycle time for the initial core was estimated at 28 to 40 h. Once the cycle is complete, H-Canyon personnel will open the <span class="hlt">dissolver</span> and probe the HFIR insert wells to determine the height of any fuel fragments which did not <span class="hlt">dissolve</span>. Before the next core can be charged to the <span class="hlt">dissolver</span>, an analysis of the potential for H 2 gas generation must show that the combined surface area of the fuel fragments and the subsequent core will not generate H 2 <span class="hlt">concentrations</span> in the <span class="hlt">dissolver</span> offgas which exceeds 60% of the lower flammability limit (LFL) of H 2 at 200 °C. The objective of this study is to identify the maximum fuel fragment height as a function of the Al <span class="hlt">concentration</span> in the <span class="hlt">dissolving</span> solution which will provide criteria for charging successive HFIR cores to an H-Canyon <span class="hlt">dissolver</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27670597','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27670597"><span>Effect of past peat cultivation practices on present dynamics of <span class="hlt">dissolved</span> organic carbon.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Frank, S; Tiemeyer, B; Bechtold, M; Lücke, A; Bol, R</p> <p>2017-01-01</p> <p>Peatlands are a major source of <span class="hlt">dissolved</span> organic carbon (DOC) for aquatic ecosystems. Naturally high DOC <span class="hlt">concentrations</span> in peatlands may be increased further by drainage. For agricultural purposes, peat has frequently been mixed with sand, but the effect of this measure on the release and cycling of DOC has rarely been investigated. This study examined the effects of (i) mixing peat with sand and (ii) water table depth (WTD) on DOC <span class="hlt">concentrations</span> at three grassland sites on shallow organic soils. The soil solution was sampled bi-weekly for two years with suction plates at 15, 30 and 60cm depth. Selected samples were analysed for <span class="hlt">dissolved</span> organic nitrogen (DON), δ 13 C DOM and δ 15 N DOM . Average DOC <span class="hlt">concentrations</span> were surprisingly high, ranging from 161 to 192mgl -1 . There was no significant impact of soil organic carbon (SOC) content or WTD on mean DOC <span class="hlt">concentrations</span>. At all sites, DOC <span class="hlt">concentrations</span> were highest at the boundary between the SOC-rich horizon and the mineral subsoil. In contrast to the mean <span class="hlt">concentrations</span>, the temporal patterns of DOC <span class="hlt">concentrations</span>, their drivers and the properties of <span class="hlt">dissolved</span> organic matter (DOM) differed between peat-sand mixtures and peat. DOC <span class="hlt">concentrations</span> responded to changes in environmental conditions, but only after a lag period of a few weeks. At the sites with a peat-sand mixture, temperature and therefore probably biological activity determined the DOC <span class="hlt">concentrations</span>. At the peat site, the contribution of vegetation-derived DOM was higher. The highest <span class="hlt">concentrations</span> occurred during long, cool periods of waterlogging, suggesting a stronger physicochemical-based DOC mobilisation. Overall, these results indicate that mixing peat with sand does not improve water quality and may result in DOC losses of around 200kg DOCha -1 a -1 . Copyright © 2016 Office national des forêts. Published by Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017NatGe..10..195F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017NatGe..10..195F"><span>Iron persistence in a distal hydrothermal plume supported by <span class="hlt">dissolved</span>-particulate exchange</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fitzsimmons, Jessica N.; John, Seth G.; Marsay, Christopher M.; Hoffman, Colleen L.; Nicholas, Sarah L.; Toner, Brandy M.; German, Christopher R.; Sherrell, Robert M.</p> <p>2017-02-01</p> <p>Hydrothermally sourced <span class="hlt">dissolved</span> metals have been recorded in all ocean basins. In the oceans' largest known hydrothermal plume, extending westwards across the Pacific from the Southern East Pacific Rise, <span class="hlt">dissolved</span> iron and manganese were shown by the GEOTRACES program to be transported halfway across the Pacific. Here, we report that particulate iron and manganese in the same plume also exceed background <span class="hlt">concentrations</span>, even 4,000 km from the vent source. Both <span class="hlt">dissolved</span> and particulate iron deepen by more than 350 m relative to 3He--a non-reactive tracer of hydrothermal input--crossing isopycnals. Manganese shows no similar descent. Individual plume particle analyses indicate that particulate iron occurs within low-density organic matrices, consistent with its slow sinking rate of 5-10 m yr-1. Chemical speciation and isotopic composition analyses reveal that particulate iron consists of Fe(III) oxyhydroxides, whereas <span class="hlt">dissolved</span> iron consists of nanoparticulate Fe(III) oxyhydroxides and an organically complexed iron phase. The descent of plume-<span class="hlt">dissolved</span> iron is best explained by reversible exchange onto slowly sinking particles, probably mediated by organic compounds binding iron. We suggest that in ocean regimes with high particulate iron loadings, <span class="hlt">dissolved</span> iron fluxes may depend on the balance between stabilization in the <span class="hlt">dissolved</span> phase and the reversibility of exchange onto sinking particles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EPJWC.14004006I','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EPJWC.14004006I"><span>Clustering impact regime with shocks in <span class="hlt">freely</span> evolving granular gas</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Isobe, Masaharu</p> <p>2017-06-01</p> <p>A <span class="hlt">freely</span> cooling granular gas without any external force evolves from the initial homogeneous state to the inhomogeneous clustering state, at which the energy decay deviates from the Haff's law. The asymptotic behavior of energy in the inelastic hard sphere model have been predicted by several theories, which are based on the mode coupling theory or extension of inelastic hard rods gas. In this study, we revisited the clustering regime of <span class="hlt">freely</span> evolving granular gas via large-scale molecular dynamics simulation with up to 16.7 million inelastic hard disks. We found novel regime regarding on collisions between "clusters" spontaneously appearing after clustering regime, which can only be identified more than a few million particles system. The volumetric dilatation pattern of semicircular shape originated from density shock propagation are well characterized on the appearing of "cluster impact" during the aggregation process of clusters.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70018246','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70018246"><span><span class="hlt">Concentration</span> history during pumping from a leaky aquifer with stratified initial <span class="hlt">concentration</span></span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Goode, Daniel J.; Hsieh, Paul A.; Shapiro, Allen M.; Wood, Warren W.; Kraemer, Thomas F.</p> <p>1993-01-01</p> <p>Analytical and numerical solutions are employed to examine the <span class="hlt">concentration</span> history of a <span class="hlt">dissolved</span> substance in water pumped from a leaky aquifer. Many aquifer systems are characterized by stratification, for example, a sandy layer overlain by a clay layer. To obtain information about separate hydrogeologic units, aquifer pumping tests are often conducted with a well penetrating only one of the layers. When the initial <span class="hlt">concentration</span> distribution is also stratified (the <span class="hlt">concentration</span> varies with elevation only), the <span class="hlt">concentration</span> breakthrough in the pumped well may be interpreted to provide information on aquifer hydraulic and transport properties. To facilitate this interpretation, we present some simple analytical and numerical solutions for limiting cases and illustrate their application to a fractured bedrock/glacial drift aquifer system where the solute of interest is <span class="hlt">dissolved</span> radon gas. In addition to qualitative information on water source, this method may yield estimates of effective porosity and saturated thickness (or fracture transport aperture) from a single-hole test. Little information about dispersivity is obtained because the measured <span class="hlt">concentration</span> is not significantly affected by dispersion in the aquifer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/862552','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/servlets/purl/862552"><span><span class="hlt">Dissolver</span> vessel bottom assembly</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Kilian, Douglas C.</p> <p>1976-01-01</p> <p>An improved bottom assembly is provided for a nuclear reactor fuel reprocessing <span class="hlt">dissolver</span> vessel wherein fuel elements are <span class="hlt">dissolved</span> as the initial step in recovering fissile material from spent fuel rods. A shock-absorbing crash plate with a convex upper surface is disposed at the bottom of the <span class="hlt">dissolver</span> vessel so as to provide an annular space between the crash plate and the <span class="hlt">dissolver</span> vessel wall. A sparging ring is disposed within the annular space to enable a fluid discharged from the sparging ring to agitate the solids which deposit on the bottom of the <span class="hlt">dissolver</span> vessel and accumulate in the annular space. An inlet tangential to the annular space permits a fluid pumped into the annular space through the inlet to flush these solids from the <span class="hlt">dissolver</span> vessel through tangential outlets oppositely facing the inlet. The sparging ring is protected against damage from the impact of fuel elements being charged to the <span class="hlt">dissolver</span> vessel by making the crash plate of such a diameter that the width of the annular space between the crash plate and the vessel wall is less than the diameter of the fuel elements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/1299255','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/1299255"><span>Salivary pH while <span class="hlt">dissolving</span> vitamin C-containing tablets.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hays, G L; Bullock, Q; Lazzari, E P; Puente, E S</p> <p>1992-10-01</p> <p>Vitamin C is packaged in numerous forms which allow protracted exposure of the teeth to ascorbic acid. The repeated use of chewable mega dose tablets of vitamin C as a mint can damage the teeth by <span class="hlt">dissolving</span> the enamel. In the time it takes to <span class="hlt">dissolve</span> a chewable vitamin C tablet, a salivary pH drop takes place; salivary calcium and phosphorus ion <span class="hlt">concentration</span> drops, and enamel dissolution may begin. Although sodium ascorbate, a buffering agent, is present in many vitamin C products, it may be added in insufficient quantity to be effective. With no apparent therapeutic value from topical vitamin C, vitamin C-containing products should be swallowed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28448934','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28448934"><span>Release of <span class="hlt">dissolved</span> phosphorus from riparian wetlands: Evidence for complex interactions among hydroclimate variability, topography and soil properties.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gu, Sen; Gruau, Gérard; Dupas, Rémi; Rumpel, Cornélia; Crème, Alexandra; Fovet, Ophélie; Gascuel-Odoux, Chantal; Jeanneau, Laurent; Humbert, Guillaume; Petitjean, Patrice</p> <p>2017-11-15</p> <p>In agricultural landscapes, establishment of vegetated buffer zones in riparian wetlands (RWs) is promoted to decrease phosphorus (P) emissions because RWs can trap particulate P from upslope fields. However, long-term accumulation of P risks the release of <span class="hlt">dissolved</span> P, since the unstable hydrological conditions in these zones may mobilize accumulated particulate P by transforming it into a mobile <span class="hlt">dissolved</span> P species. This study evaluates how hydroclimate variability, topography and soil properties interact and influence this mobilization, using a three-year dataset of molybdate-reactive <span class="hlt">dissolved</span> P (MRDP) and total <span class="hlt">dissolved</span> P (TDP) <span class="hlt">concentrations</span> in soil water from two RWs located in an agricultural catchment in western France (Kervidy-Naizin), along with stream P <span class="hlt">concentrations</span>. Two main drivers of seasonal <span class="hlt">dissolved</span> P release were identified: i) soil rewetting during water-table rise after dry periods and ii) reductive dissolution of soil Fe (hydr)oxides during prolonged water saturation periods. These mechanisms were shown to vary greatly in space (according to topography) and time (according to intra- and interannual hydroclimate variability). The <span class="hlt">concentration</span> and speciation of the released <span class="hlt">dissolved</span> P also varied spatially depending on soil chemistry and local topography. Comparison of sites revealed a similar correlation between soil P speciation (percentage of organic P ranging from 35-70%) and the <span class="hlt">concentration</span> and speciation of the released P (MRDP from <0.10 to 0.40mgl -1 ; percentage of MRDP in TDP from 25-70%). These differences propagated to stream water, suggesting that the two RWs investigated were the main sources of <span class="hlt">dissolved</span> P to streams. RWs can be critical areas due to their ability to biogeochemically transform the accumulated P in these zones into highly mobile and highly bioavailable <span class="hlt">dissolved</span> P forms. Hydroclimate variability, local topography and soil chemistry must be considered to decrease the risk of remobilizing legacy soil P when</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009APS..DFD.BN009O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009APS..DFD.BN009O"><span>Global Visualization in Water using AnodizedAluminum PressureSensitive Paint and <span class="hlt">Dissolved</span> Oxygen as Tracer</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ozaki, Tatsuya; Ishikawa, Hitoshi; Sakaue, Hirotaka</p> <p>2009-11-01</p> <p>We have developed anodized-aluminum pressuresensitive paint (AA-PSP) for flow visualization in water using <span class="hlt">dissolved</span> oxygen as a tracer. Developed AA-PSP is characterized using water calibration setup by controlling a <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span>. It is shown that the developed AA-PSP gives 4.0 percent change in luminescence per 1 mg/l of oxygen <span class="hlt">concentration</span>. This AA-PSP is applied to visualize flows in a water tunnel. Oxygen <span class="hlt">concentrations</span> of the water tunnel and the <span class="hlt">dissolved</span> oxygen are 9.5 mg/l and 20 mg/l, respectively. We can capture horseshoe vortices over the base of 10 mm cylinder by using this technique at Reynolds number of 1000 and a water speed of 100 mm/s, respectively. Unlike conventional tracers such as ink, milk, and fluorescent dyes, this visualization technique gives flow information on the AA-PSP coated surface without integrating flows between the AA-PSP and an optical detector. Because of using <span class="hlt">dissolved</span> oxygen as a tracer, it holds the material properties of testing water except for the amount of oxygen. The tracer does not interfere with optical measurements and it does not contaminate the testing water. A conventional visualization technique using milk as a tracer is also employed for comparison.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17448175','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17448175"><span>Characterization of two ammonia-oxidizing bacteria isolated from reactors operated with low <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Park, H-D; Noguera, D R</p> <p>2007-05-01</p> <p>To obtain ammonia-oxidizing bacterial (AOB) strains inhabiting low <span class="hlt">dissolved</span> oxygen (DO) environments and to characterize them to better understand their function and ecology. Using a serial dilution method, two AOB strains (ML1 and NL7) were isolated from chemostat reactors operated with low DO <span class="hlt">concentrations</span> (0.12-0.24 mg l(-1)). Phylogenetically, strains ML1 and NL7 are affiliated to AOB within the Nitrosomonas europaea and Nitrosomonas oligotropha lineages, respectively. Kinetically, strain ML1 had high affinity for oxygen (0.24 +/- 0.13 mg l(-1)) and low affinity for ammonia (1.62 +/- 0.97 mg N l(-1)), while strain NL7 had high affinity for ammonia (0.48 +/- 0.35 mg l(-1)), but a surprisingly low affinity for oxygen (1.22 +/- 0.43 mg l(-1)). A co-culture experiment was used to iteratively estimate decay constants for both strains. The results indicated that AOB without high affinity for oxygen may have other mechanisms to persist in low DO environments, with high affinity for ammonia being important. This study provides a method to determine AOB growth kinetic parameters without assuming or neglecting decay constant. And, this is the first report on oxygen affinity constant of a N. oligotropha strain.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18776612','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18776612"><span><span class="hlt">Dissolved</span> oxygen as a key parameter to aerobic granule formation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Sturm, B S McSwain; Irvine, R L</p> <p>2008-01-01</p> <p>Much research has asserted that high shear forces are necessary for the formation of aerobic granular sludge in Sequencing Batch Reactors (SBRs). In order to distinguish the role of shear and <span class="hlt">dissolved</span> oxygen on granule formation, two separate experiments were conducted with three bench-scale SBRs. In the first experiment, an SBR was operated with five sequentially decreasing superficial upflow gas velocities ranging from 1.2 to 0.4 cm s(-1). When less than 1 cm s(-1) shear was applied to the reactor, aerobic granules disintegrated into flocs, with corresponding increases in SVI and effluent suspended solids. However, the <span class="hlt">dissolved</span> oxygen also decreased from 8 mg L(-1) to 5 mg L(-1), affecting the Feast/Famine regime in the SBR and the substrate removal kinetics. A second experiment operated two SBRs with an identical shear force of 1.2 cm s(-1), but two <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>. Even when supplied a high shear force, aerobic granules could not form at a <span class="hlt">dissolved</span> oxygen less than 5 mg L(-1), with a Static Fill. These results indicate that the substrate removal kinetics and <span class="hlt">dissolved</span> oxygen are more significant to granule formation than shear force. Copyright IWA Publishing 2008.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25753259','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25753259"><span>The effect of <span class="hlt">dissolved</span> oxygen on the susceptibility of blood.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Berman, Avery J L; Ma, Yuhan; Hoge, Richard D; Pike, G Bruce</p> <p>2016-01-01</p> <p>It has been predicted that, during hyperoxia, excess O2 <span class="hlt">dissolved</span> in arterial blood will significantly alter the blood's magnetic susceptibility. This would confound the interpretation of the hyperoxia-induced blood oxygenation level-dependent signal as arising solely from changes in deoxyhemoglobin. This study, therefore, aimed to determine how <span class="hlt">dissolved</span> O2 affects the susceptibility of blood. We present a comprehensive model for the effect of <span class="hlt">dissolved</span> O2 on the susceptibility of blood and compare it with another recently published model, referred to here as the ideal gas model (IGM). For validation, distilled water and samples of bovine plasma were oxygenated over a range of hyperoxic O2 <span class="hlt">concentrations</span> and their susceptibilities were determined using multiecho gradient echo phase imaging. In distilled water and plasma, the measured changes in susceptibility were very linear, with identical slopes of 0.062 ppb/mm Hg of O2. This change was dramatically less than previously predicted using the IGM and was close to that predicted by our model. The primary source of error in the IGM is the overestimation of the volume fraction occupied by <span class="hlt">dissolved</span> O2. Under most physiological conditions, the susceptibility of <span class="hlt">dissolved</span> O2 can be disregarded in MRI studies employing hyperoxia. © 2015 Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1343524-seasonal-flow-driven-dynamics-particulate-dissolved-mercury-methylmercury-stream-impacted-industrial-mercury-source','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1343524-seasonal-flow-driven-dynamics-particulate-dissolved-mercury-methylmercury-stream-impacted-industrial-mercury-source"><span>Seasonal and flow-driven dynamics of particulate and <span class="hlt">dissolved</span> mercury and methylmercury in a stream impacted by an industrial mercury source</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Riscassi, Ami; Miller, Carrie; Brooks, Scott</p> <p>2015-11-17</p> <p>Sediments and floodplain soils in the East Fork Poplar Creek watershed (Oak Ridge, TN, USA) are contaminated with high levels of mercury (Hg) from an industrial source at the headwaters. Although baseflow conditions have been monitored, <span class="hlt">concentrations</span> of Hg and methylmercury (MeHg) during high-flow storm events, when the stream is more hydrologically connected to the floodplain, have yet to be assessed. This paper evaluated baseflow and event-driven Hg and MeHg dynamics in East Fork Poplar Creek, 5 km upstream of the confluence with Poplar Creek, to determine the importance of hydrology to in-stream <span class="hlt">concentrations</span> and downstream loads and to ascertainmore » whether the dynamics are comparable to those of systems without an industrial Hg source. Particulate Hg and MeHg were positively correlated with discharge (r 2 = 0.64 and 0.58, respectively) and total suspended sediment (r 2 = 0.97 and 0.89, respectively), and <span class="hlt">dissolved</span> Hg also increased with increasing flow (r 2 = 0.18) and was associated with increases in <span class="hlt">dissolved</span> organic carbon (r 2 = 0.65), similar to the dynamics observed in uncontaminated systems. <span class="hlt">Dissolved</span> MeHg decreased with increases in discharge (r 2 = 0.23) and was not related to <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> (p = 0.56), dynamics comparable to relatively uncontaminated watersheds with a small percentage of wetlands (<10%). Finally, although stormflows exert a dominant control on particulate Hg, particulate MeHg, and <span class="hlt">dissolved</span> Hg <span class="hlt">concentrations</span> and loads, baseflows were associated with the highest <span class="hlt">dissolved</span> MeHg <span class="hlt">concentration</span> (0.38 ng/L) and represented the majority of the annual <span class="hlt">dissolved</span> MeHg load.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27871745','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27871745"><span>The effect of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (DO) on oxygen diffusion and bacterial community structure in moving bed sequencing batch reactor (MBSBR).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cao, Yongfeng; Zhang, Chaosheng; Rong, Hongwei; Zheng, Guilin; Zhao, Limin</p> <p>2017-01-01</p> <p>The effect of <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> (DO) on simultaneous nitrification and denitrification was studied in a moving bed sequencing batch reactor (MBSBR) by microelectrode measurements and by real-time PCR. In this system, the biofilm grew on polyurethane foam carriers used to treat municipal sewage at five DO <span class="hlt">concentrations</span> (1.5, 2.5, 3.5, 4.5 and 5.5 mg/L). The results indicated that the MBSBR exhibited good removal of chemical oxygen demand (92.43%) and nitrogen (83.73%) when DO <span class="hlt">concentration</span> was 2.5 mg/L. Increasing the oxygen <span class="hlt">concentration</span> in the reactor was inhibitory to denitrification. Microelectrode measurements showed that the thickness of oxygen penetration increased from 1.2 to 2.6 mm when the DO <span class="hlt">concentration</span> (from 1.5 mg/L to 5.5 mg/L) in the system increased. Oxygen diffusion was not significantly limited by the boundary layer surrounding the carrier and had the largest slope when DO <span class="hlt">concentration</span> was 2.5 mg/L. The real-time PCR analysis indicated that the amount of the ammonia-oxidizing bacteria and nitrite-oxidizing bacteria increased slowly as DO <span class="hlt">concentration</span> increased. The proportions of ammonia-oxidizing bacteria and nitrite-oxidizing bacteria, as a percentage of the total bacteria, were low with average values of 0.063% and 0.67%, respectively. When the DO <span class="hlt">concentration</span> was 2.5 mg/L, oxygen diffusion was optimal and ensured the optimal bacterial community structure and activity; under these conditions, the MBSBR was efficient for total inorganic nitrogen removal. Changing the DO <span class="hlt">concentration</span> could alter the aerobic zone and the bacterial community structure in the biofilm, directly influencing the simultaneous nitrification and denitrification activity in MBSBRs. Copyright © 2016 Elsevier Ltd. All rights reserved.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_19 --> <div id="page_20" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="381"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=34289&Lab=NHEERL&keyword=temperature+AND+oxygen+AND+consumption&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=34289&Lab=NHEERL&keyword=temperature+AND+oxygen+AND+consumption&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>SIMULATION OF <span class="hlt">DISSOLVED</span> OXYGEN PROFILES IN A TRANSPARENT, DIMICTIC LAKE</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Thrush Lake is a small, highly transparent lake in northeastern Minnesota. rom 1986 to 1991, vertical profiles of water temperature, <span class="hlt">dissolved</span> oxygen, chlorophyll a <span class="hlt">concentration</span>, underwater light irradiance, and Secchi depths were measured at monthly intervals during the ice-fre...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2006CSR....26.1654W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2006CSR....26.1654W"><span>Distributions of nutrients, <span class="hlt">dissolved</span> organic carbon and carbohydrates in the western Arctic Ocean</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, Deli; Henrichs, Susan M.; Guo, Laodong</p> <p>2006-09-01</p> <p>Seawater samples were collected from stations along a transect across the shelf-basin interface in the western Arctic Ocean during September 2002, and analyzed for nutrients, <span class="hlt">dissolved</span> organic carbon (DOC), and total <span class="hlt">dissolved</span> carbohydrate (TDCHO) constituents, including monosaccharides (MCHO) and polysaccharides (PCHO). Nutrients (nitrate, ammonium, phosphate and <span class="hlt">dissolved</span> silica) were depleted at the surface, especially nitrate. Their <span class="hlt">concentrations</span> increased with increasing depth, with maxima centered at ˜125 m depth within the halocline layer, then decreased with increasing depth below the maxima. Both ammonium and phosphate <span class="hlt">concentrations</span> were elevated in shelf bottom waters, indicating a possible nutrient source from sediments, and in a plume that extended into the upper halocline waters offshore. <span class="hlt">Concentrations</span> of DOC ranged from 45 to 85 μM and had an inverse correlation with salinity, indicating that mixing is a control on DOC <span class="hlt">concentrations</span>. <span class="hlt">Concentrations</span> of TDCHO ranged from 2.5 to 19 μM-C, comprising 13-20% of the bulk DOC. Higher DOC <span class="hlt">concentrations</span> were found in the upper water column over the shelf along with higher TDCHO <span class="hlt">concentrations</span>. Within the TDCHO pool, the <span class="hlt">concentrations</span> of MCHO ranged from 0.4 to 8.6 μM-C, comprising 20-50% of TDCHO, while PCHO <span class="hlt">concentrations</span> ranged from 0.5 to 13.6 μM-C, comprising 50-80% of the TDCHO. The MCHO/TDCHO ratio was low in the upper 25 m of the water column, followed by a high MCHO/TDCHO ratio between 25 and 100 m, and a low MCHO/TDCHO ratio again below 100 m. The high MCHO/TDCHO ratio within the halocline layer likely resulted from particle decomposition and associated release of MCHO, whereas the low MCHO/TDCHO (or high PCHO/TDCHO) ratio below the halocline layer could have resulted from slow decomposition and additional particulate CHO sources.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/4304923','DOE-PATENT-XML'); return false;" href="https://www.osti.gov/biblio/4304923"><span>PROCESS OF <span class="hlt">DISSOLVING</span> ZIRCONIUM ALLOYS</span></a></p> <p><a target="_blank" href="http://www.osti.gov/doepatents">DOEpatents</a></p> <p>Shor, R.S.; Vogler, S.</p> <p>1958-01-21</p> <p>A process is described for <span class="hlt">dissolving</span> binary zirconium-uranium alloys where the uranium content is about 2%. In prior dissolution procedures for these alloys, an oxidizing agent was added to prevent the precipitation of uranium tetrafluoride. In the present method complete dissolution is accomplished without the use of the oxidizing agent by using only the stoichiometric amount or slight excess of HF required by the zirconium. The <span class="hlt">concentration</span> of the acid may range from 2M to 10M and the dissolution is advatageously carried out at a temperature of 80 deg C.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JMS...180..289N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JMS...180..289N"><span>Enhanced <span class="hlt">dissolved</span> lipid production as a response to the sea surface warming</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Novak, Tihana; Godrijan, Jelena; Pfannkuchen, Daniela Marić; Djakovac, Tamara; Mlakar, Marina; Baricevic, Ana; Tanković, Mirta Smodlaka; Gašparović, Blaženka</p> <p>2018-04-01</p> <p>The temperature increase in oceans reflects on marine ecosystem functioning and surely has consequences on the marine carbon cycle and carbon sequestration. In this study, we examined <span class="hlt">dissolved</span> lipid, lipid classes and <span class="hlt">dissolved</span> organic carbon (DOC) production in the northern Adriatic Sea, isolated diatom Chaetoceros pseudocurvisetus batch cultures grown in a wide temperature range (10-30 °C) and in contrasting nutrient regimes, phosphorus (P)-depleted and P-replete conditions. Additionally, lipids and DOC were analyzed in the northern Adriatic (NA) in two stations characterized with different P availability, occupied from February to August 2010 that covered a temperature range from 9.3 to 31.1 °C. To gain insight into factors governing lipid and lipid classes' production in the NA, apart from temperature (T), Chlorophyll a, phytoplankton community abundance and structure, nutrient <span class="hlt">concentrations</span> were measured together with hydrographic parameters. We found enhanced accumulation of <span class="hlt">dissolved</span> lipids, particulary glycolipids, with increasing T, especially during the highest in situ temperature. The effect of T on enhanced <span class="hlt">dissolved</span> lipid release is much more pronounced under P-deplete conditions indicating that oligotrophic regions might be more vulnerable to T rise. Temperature between 25 and 30 °C is a threshold T range for C. pseudocurvisetus, at which a significant part of lipid production is directed toward the <span class="hlt">dissolved</span> phase. Unlike monocultures, there are multiple factors influencing produced lipid composition, distribution and cycling in the NA that may counteract the T influence. The possible role of enhanced <span class="hlt">dissolved</span> lipid <span class="hlt">concentration</span> for carbon sequestration at elevated T is discussed. On the one hand, lipids are buoyant and do not sink, which enhances their retention at the surface layer. In addition, they are surface active, and therefore prone to adsorb on sinking particles, contributing to the C sequestration.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43D2159S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43D2159S"><span>A Novel Method for Analysis of <span class="hlt">Dissolved</span> Inorganic Carbon <span class="hlt">Concentration</span> and δ13C by Cavity Ring-Down Spectroscopy</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Smith, E.; Gonneea, M. E.; Boze, L. G.; Casso, M.; Pohlman, J.</p> <p>2017-12-01</p> <p><span class="hlt">Dissolved</span> inorganic carbon (DIC) is the largest pool of carbon in the oceans and is where about half of anthropogenic carbon dioxide (CO2) emissions are being sequestered. Determining the <span class="hlt">concentration</span> and stable carbon isotopic content (δ13C) of DIC allows us to delineate carbon sources that contribute to marine DIC. A simple and reliable method for measuring DIC <span class="hlt">concentration</span> and δ13C can be used to apportion contributions from external sources and identify effects from biogeochemical reactions that contribute or remove DIC. The U.S. Geological Survey has developed a discrete sample analysis module (DSAM) that interfaces to a Picarro G-2201i cavity ring-down spectrometer (CRDS, Picarro Inc.) to analyze CO2 and methane <span class="hlt">concentrations</span> and δ13C from discrete gas samples. In this study, we adapted the USGS DSAM-CRDS analysis system to include an AutoMate prep device (Automate FX, Inc.) for analysis of DIC <span class="hlt">concentration</span> and δ13C from aqueous samples. The Automate prep device was modified to deliver CO2 extracted from DIC to the DSAM, which conditions and transfers the gas to the CRDS. LabVIEW software (National Instruments) triggers the Automate Prep device, controls the DSAM and collects data from the CRDS. CO2 mass <span class="hlt">concentration</span> data are obtained by numerical integration of the CO2 volumetric <span class="hlt">concentrations</span> output by the CRDS and subsequent comparison to standard materials. CO2 carbon isotope values from the CRDS (iCO2) are converted to δ13C values using a slope and offset correction calibration procedure. The system design and operation was optimized using sodium bicarbonate (NaHCO3) standards and a certified reference material. Surface water and pore water samples collected from Sage Lot Pond, a salt marsh in Cape Cod MA, have been analyzed for <span class="hlt">concentration</span> by coulometry and δ13C by isotope ratio mass spectrometry and will be used to validate the DIC-DSAM-CRDS method for field applications.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/47057','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/47057"><span>Overstory vegetation influence nitrogen and <span class="hlt">dissolved</span> organic carbon flux from the atmosphere to the forest floor: Boreal Plain, Canada</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>David E. Pelster; Randall K. Kolka; Ellie E. Prepas</p> <p>2009-01-01</p> <p>Nitrate, ammonium, total <span class="hlt">dissolved</span> nitrogen (TDN), <span class="hlt">dissolved</span> organic nitrogen (DON) and <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentrations</span> and flux were measured for one year in bulk deposition and throughfall from three stand types (upland deciduous, upland conifer and wetland conifer) on the Boreal Plain, Canada. Annual (November 2006 to October 2007 water year) flux...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..1914234S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..1914234S"><span><span class="hlt">Dissolved</span> strontium and calcium levels in the tropical Indian Ocean</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Steiner, Zvi; Sarkar, Amit; Turchyn, Alexandra</p> <p>2017-04-01</p> <p>Measurements of seawater alkalinity and <span class="hlt">dissolved</span> calcium <span class="hlt">concentrations</span> along oceanic transects are often used to calculate calcium carbonate precipitation and dissolution rates. Given that the distribution coefficient of strontium in CaCO3 varies greatly between different groups of organisms, adding precise measurements of <span class="hlt">dissolved</span> strontium <span class="hlt">concentrations</span> provides opportunities to also track relative contributions of these different groups to the regional CaCO3 cycle. However, there are several obstacles to this approach. These obstacles include unresolved systematic discrepancies between seawater calcium and alkalinity data, very large analytical noise around the calcium <span class="hlt">concentration</span> measurements and the unconstrained role of acantharia (radiolarian precipitating SrSO4 skeletons) in the marine strontium cycle. During the first cruise of the second International Indian Ocean Expedition (IIOE-2) water samples were collected along 67°E from 9°N to 5°S to explore the dissolution rate of calcium carbonate in the water. The dissolution rate can be calculated by combining measurements of water column potential alkalinity with calcium and strontium <span class="hlt">concentrations</span> measured by ICP-OES and calcium <span class="hlt">concentration</span> measurements using isotope dilution thermal ionization mass spectrometry (ID-TIMS). CaCO3 mineral saturation state calculated using pH and total alkalinity suggests that along 67°E, the aragonite saturation horizon lays at depth of 500 m on both sides of the equator. Across the cruise transect, <span class="hlt">dissolved</span> strontium <span class="hlt">concentrations</span> increase by 2-3% along the thermocline suggesting rapid recycling of strontium rich phases. This is particularly evident just below the thermocline at 8-9°N and below 1000 m water depth, south of the equator. The deep, southern enrichment in strontium does not involve a change in the Sr/Ca ratio, suggesting that this strontium enrichment is related to CaCO3 dissolution. In contrast, in the intermediate waters of the northern part of</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23422138','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23422138"><span>Minimizing residual aluminum <span class="hlt">concentration</span> in treated water by tailoring properties of polyaluminum coagulants.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kimura, Masaoki; Matsui, Yoshihiko; Kondo, Kenta; Ishikawa, Tairyo B; Matsushita, Taku; Shirasaki, Nobutaka</p> <p>2013-04-15</p> <p>Aluminum coagulants are widely used in water treatment plants to remove turbidity and <span class="hlt">dissolved</span> substances. However, because high aluminum <span class="hlt">concentrations</span> in treated water are associated with increased turbidity and because aluminum exerts undeniable human health effects, its <span class="hlt">concentration</span> should be controlled in water treatment plants, especially in plants that use aluminum coagulants. In this study, the effect of polyaluminum chloride (PACl) coagulant characteristics on <span class="hlt">dissolved</span> residual aluminum <span class="hlt">concentrations</span> after coagulation and filtration was investigated. The <span class="hlt">dissolved</span> residual aluminum <span class="hlt">concentrations</span> at a given coagulation pH differed among the PACls tested. Very-high-basicity PACl yielded low <span class="hlt">dissolved</span> residual aluminum <span class="hlt">concentrations</span> and higher natural organic matter (NOM) removal. The low residual aluminum <span class="hlt">concentrations</span> were related to the low content of monomeric aluminum (Ala) in the PACl. Polymeric (Alb)/colloidal (Alc) ratio in PACl did not greatly influence residual aluminum <span class="hlt">concentration</span>. The presence of sulfate in PACl contributed to lower residual aluminum <span class="hlt">concentration</span> only when coagulation was performed at around pH 6.5 or lower. At a wide pH range (6.5-8.5), residual aluminum <span class="hlt">concentrations</span> <0.02 mg/L were attained by tailoring PACl properties (Ala percentage ≤0.5%, basicity ≥85%). The <span class="hlt">dissolved</span> residual aluminum <span class="hlt">concentrations</span> did not increase with increasing the dosage of high-basicity PACl, but did increase with increasing the dosage of normal-basicity PACl. We inferred that increasing the basicity of PACl afforded lower <span class="hlt">dissolved</span> residual aluminum <span class="hlt">concentrations</span> partly because the high-basicity PACls could have a small percentage of Ala, which tends to form soluble aluminum-NOM complexes with molecular weights of 100 kDa-0.45 μm. Copyright © 2013 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=65546&keyword=boat&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=65546&keyword=boat&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>TOTAL <span class="hlt">DISSOLVED</span> AND BIOAVAILABLE METALS AT LAKE TEXOMA MARINAS</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p><span class="hlt">Dissolved</span> metals in water and total metals in sediments have been measured at marina areas in Lake Texoma during June 1999 to October 2001, and October 2001, respectively. The metals most often found in the highest <span class="hlt">concentrations</span> in marina water were Na and Ca, followed by Mg an...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1988PhRvB..3812868H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1988PhRvB..3812868H"><span><span class="hlt">Freely</span>-migrating-defect production during irradiation at elevated temperatures</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hashimoto, T.; Rehn, L. E.; Okamoto, P. R.</p> <p>1988-12-01</p> <p>Radiation-induced segregation in a Cu-1 at. % Au alloy was investigated using in situ Rutherford backscattering spectrometry. The amount of Au atom depletion in the near surface region was measured as a function of dose during irradiation at 350 °C with four ions of substantially different masses. Relative efficiencies for producing <span class="hlt">freely</span> migrating defects were evaluated for 1.8-MeV 1H, 4He, 20Ne, and 84Kr ions by determining beam current densities that gave similar radiation-induced segregation rates. Irradiations with primary knock-on atom median energies of 1.7, 13, and 79 keV yielded relative efficiencies of 53, 7, and 6 %, respectively, compared to the irradiation with a 0.83-keV median energy. Despite quite different defect and host alloy properties, the relative efficiencies for producing <span class="hlt">freely</span> migrating defects determined in Cu-Au are remarkably similar to those found previously in Ni-Si alloys. Hence, the reported efficiencies appear to offer a reliable basis for making quantitative correlations of microstructural changes induced in different alloy systems by a wide variety of irradiation particles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20140005468','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20140005468"><span>Remote Sensing of <span class="hlt">Dissolved</span> Oxygen and Nitrogen in Water Using Raman Spectroscopy</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Ganoe, Rene; DeYoung, Russell J.</p> <p>2013-01-01</p> <p>The health of an estuarine ecosystem is largely driven by the abundance of <span class="hlt">dissolved</span> oxygen and nitrogen available for maintenance of plant and animal life. An investigation was conducted to quantify the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> molecular oxygen and nitrogen in water by means of Raman spectroscopy. This technique is proposed for the remote sensing of <span class="hlt">dissolved</span> oxygen in the Chesapeake Bay, which will be utilized by aircraft in order to survey large areas in real-time. A proof of principle system has been developed and the specifications are being honed to maximize efficiency for the final application. The theoretical criteria of the research, components of the experimental system, and key findings are presented in this report</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24720192','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24720192"><span>[Geochemical distribution of <span class="hlt">dissolved</span> bismuth in the Yellow Sea and East China Sea].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wu, Xiao-Dan; Song, Jin-Ming; Wu, Bin; Li, Xue-Gang</p> <p>2014-01-01</p> <p>Occurrence level, geochemical distribution of <span class="hlt">dissolved</span> bismuth and its coupling relationship to eco-environment were investigated in the Yellow Sea and East China Sea to explore the source and influencing factors. The results showed that the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> bismuth was within the range of 0-0. 029 microg x L(-1) at the surface and 0.001-0.189 microg x L(-1) at the bottom, with the averages of 0.008 and 0.016 microg x L(-1), respectively. Horizontally, low value of <span class="hlt">dissolved</span> bismuth exhibited the bidirectional extension feature, indicating that it could trace the path of Changjiang Diluted Water. High value of <span class="hlt">dissolved</span> bismuth was observed where the Subei Costal Current and Yellow Sea Warm Current flowed and the Changjiang Diluted Water and Zhejiang-Fujian Coastal Current met, suggesting that it was controlled by the cycle of current system. Vertically, the coastal water was fully mixed by water convection and eddy mixing, and was divided from the stratified water by strong tidal front, which blocked the transport of <span class="hlt">dissolved</span> bismuth to the open sea. Thus, the <span class="hlt">concentration</span> in front area was significantly higher than that in the open sea. Diurnal variation of <span class="hlt">dissolved</span> bismuth was related to the hydrodynamic conditions (tide, suspension and thermocline) instead of the environmental factors (temperature and salinity). Positive relationship to SPM (suspended particulate matter) clarified that bismuth was prone to release from solid phase to liquid phase. Furthermore, conditions with temperature ranging 22-27 degrees C, salinity ranging 28-31 and pH ranging 7.9-8.1 were shown to be optimal for the release process.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4143086','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4143086"><span>Long-term Behavioral Tracking of <span class="hlt">Freely</span> Swimming Weakly Electric Fish</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Jun, James J.; Longtin, André; Maler, Leonard</p> <p>2014-01-01</p> <p>Long-term behavioral tracking can capture and quantify natural animal behaviors, including those occurring infrequently. Behaviors such as exploration and social interactions can be best studied by observing unrestrained, <span class="hlt">freely</span> behaving animals. Weakly electric fish (WEF) display readily observable exploratory and social behaviors by emitting electric organ discharge (EOD). Here, we describe three effective techniques to synchronously measure the EOD, body position, and posture of a free-swimming WEF for an extended period of time. First, we describe the construction of an experimental tank inside of an isolation chamber designed to block external sources of sensory stimuli such as light, sound, and vibration. The aquarium was partitioned to accommodate four test specimens, and automated gates remotely control the animals' access to the central arena. Second, we describe a precise and reliable real-time EOD timing measurement method from <span class="hlt">freely</span> swimming WEF. Signal distortions caused by the animal's body movements are corrected by spatial averaging and temporal processing stages. Third, we describe an underwater near-infrared imaging setup to observe unperturbed nocturnal animal behaviors. Infrared light pulses were used to synchronize the timing between the video and the physiological signal over a long recording duration. Our automated tracking software measures the animal's body position and posture reliably in an aquatic scene. In combination, these techniques enable long term observation of spontaneous behavior of <span class="hlt">freely</span> swimming weakly electric fish in a reliable and precise manner. We believe our method can be similarly applied to the study of other aquatic animals by relating their physiological signals with exploratory or social behaviors. PMID:24637642</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015CSR...108...12H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015CSR...108...12H"><span>Spatiotemporal variation characteristics and related affecting factors of <span class="hlt">dissolved</span> carbohydrates in the East China Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>He, Zhen; Wang, Qi; Yang, Gui-Peng; Gao, Xian-Chi; Wu, Guan-Wei</p> <p>2015-10-01</p> <p>Carbohydrates are the largest identified fraction of <span class="hlt">dissolved</span> organic carbon and play an important role in biogeochemical cycling in the ocean. Seawater samples were collected from the East China Sea (ECS) during June and October 2012 to study the spatiotemporal distributions of total <span class="hlt">dissolved</span> carbohydrates (TCHOs) constituents, including <span class="hlt">dissolved</span> monosaccharides (MCHOs) and polysaccharides (PCHOs). The <span class="hlt">concentrations</span> of TCHOs, MCHOs and PCHOs showed significant differences between summer and autumn 2012, and exhibited an evident diurnal variation, with high values occurring in the daytime. Phytoplankton biomass was identified as the primary factor responsible for seasonal and diurnal variations of <span class="hlt">dissolved</span> carbohydrates in the ECS. The TCHOs, MCHOs and PCHOs distributions in the study area displayed similar distribution patterns, with high <span class="hlt">concentrations</span> appearing in the coastal water. The influences of chlorophyll-a, salinity and nutrients on the distributions of these carbohydrates were examined. A carbohydrate enrichment in the near-bottom water was found at some stations, implying that there might be an important source of carbohydrate in the deep water or bottom sediment.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22542303','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22542303"><span>Annual variability in the radiocarbon age and source of <span class="hlt">dissolved</span> CO2 in a peatland stream.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Garnett, Mark H; Dinsmore, Kerry J; Billett, Michael F</p> <p>2012-06-15</p> <p>Radiocarbon dating has the capacity to significantly improve our understanding of the aquatic carbon cycle. In this study we used a new passive sampler to measure the radiocarbon ((14)C) and stable carbon (δ(13)C) isotopic composition of <span class="hlt">dissolved</span> CO(2) for the first time in a peatland stream throughout a complete year (May 2010-June 2011). The in-stream sampling system collected time-integrated samples of CO(2) continuously over approximately 1 month periods. The rate of CO(2) trapping was proportional to independently measured streamwater CO(2) <span class="hlt">concentrations</span>, demonstrating that passive samplers can be used to estimate the time-averaged <span class="hlt">dissolved</span> CO(2) <span class="hlt">concentration</span> of streamwater. While there was little variation and no clear trend in δ(13)CO(2) values (suggesting a consistent CO(2) source), we found a clear temporal pattern in the (14)C <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> CO(2). The (14)C age of CO(2) varied from 707±35 to 1210±39 years BP, with the youngest CO(2) in the autumn and oldest in spring/early summer. Mean stream discharge and (14)C content of <span class="hlt">dissolved</span> CO(2) were positively correlated. We suggest that the observed pattern in the (14)C content of <span class="hlt">dissolved</span> CO(2) reflects changes in its origin, with older carbon derived from deeper parts of the peat profile contributing proportionally more gaseous carbon during periods of low stream flow. Copyright © 2012 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSCT31A..08K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSCT31A..08K"><span>Distribution of <span class="hlt">dissolved</span> zinc in the western and central subarctic North Pacific</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kim, T.; Obata, H.; Gamo, T.</p> <p>2016-02-01</p> <p>Zinc (Zn) is an essential micronutrient for bacteria and phytoplankton in the ocean as it plays an important role in numerous enzyme systems involved in various metabolic processes. However, large-scale distributions of total <span class="hlt">dissolved</span> Zn in the subarctic North Pacific have not been investigated yet. In this study, we investigated the distributions of total <span class="hlt">dissolved</span> Zn to understand biogeochemical cycling of Zn in the western and central subarctic North Pacific as a Japanese GEOTRACES project. Seawater samples were collected during the R/V Hakuho-maru KH-12-4 GEOTRACES GP 02 cruise (from August to October 2012), by using acid-cleaned Teflon-coated X-type Niskin samplers. Total <span class="hlt">dissolved</span> Zn in seawater was determined using cathodic stripping voltammetry (CSV) after UV-digestion. In this study, total <span class="hlt">dissolved</span> Zn <span class="hlt">concentrations</span> in the western and central subarctic North Pacific commonly showed Zn increase from surface to approximately 400-500 m, just above the oxygen minimum layer. However, in the western subarctic North Pacific, relatively higher Zn <span class="hlt">concentrations</span> have also been observed at intermediate depths (800-1200 m), in comparison with those observed in deep waters. The relationship between Zn and Si in the western subarctic North Pacific showed that Zn is slightly enriched at intermediate depths. These results may indicate that there are additional sources of Zn to intermediate water of the western subarctic North Pacific.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26921729','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26921729"><span>Toxicity of <span class="hlt">dissolved</span> and precipitated aluminium to marine diatoms.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gillmore, Megan L; Golding, Lisa A; Angel, Brad M; Adams, Merrin S; Jolley, Dianne F</p> <p>2016-05-01</p> <p>Localised aluminium contamination can lead to high <span class="hlt">concentrations</span> in coastal waters, which have the potential for adverse effects on aquatic organisms. This research investigated the toxicity of 72-h exposures of aluminium to three marine diatoms (Ceratoneis closterium (formerly Nitzschia closterium), Minutocellus polymorphus and Phaeodactylum tricornutum) by measuring population growth rate inhibition and cell membrane damage (SYTOX Green) as endpoints. Toxicity was correlated to the time-averaged <span class="hlt">concentrations</span> of different aluminium size-fractions, operationally defined as <0.025μm filtered, <0.45μm filtered (<span class="hlt">dissolved</span>) and unfiltered (total) present in solution over the 72-h bioassay. The chronic population growth rate inhibition after aluminium exposure varied between diatom species. C. closterium was the most sensitive species (10% inhibition of growth rate (72-h IC10) of 80 (55-100)μg Al/L (95% confidence limits)) while M. polymorphus (540 (460-600)μg Al/L) and P. tricornutum (2100 (2000-2200)μg Al/L) were less sensitive (based on measured total aluminium). <span class="hlt">Dissolved</span> aluminium was the primary contributor to toxicity in C. closterium, while a combination of <span class="hlt">dissolved</span> and precipitated aluminium forms contributed to toxicity in M. polymorphus. In contrast, aluminium toxicity to the most tolerant diatom P. tricornutum was due predominantly to precipitated aluminium. Preliminary investigations revealed the sensitivity of C. closterium and M. polymorphus to aluminium was influenced by initial cell density with aluminium toxicity significantly (p<0.05) increasing with initial cell density from 10(3) to 10(5)cells/mL. No effects on plasma membrane permeability were observed for any of the three diatoms suggesting that mechanisms of aluminium toxicity to diatoms do not involve compromising the plasma membrane. These results indicate that marine diatoms have a broad range in sensitivity to aluminium with toxic mechanisms related to both <span class="hlt">dissolved</span> and precipitated</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43H2227R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43H2227R"><span><span class="hlt">Dissolved</span> Carbon Fluxes During the 2017 Mississippi River Flood</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Reiman, J. H.; Xu, Y. J.</p> <p>2017-12-01</p> <p>The Mississippi River drains approximately 3.2 million square kilometres of land and discharges about 680 cubic kilometres of water into the Northern Gulf of Mexico annually, acting as a significant medium for carbon transport from land to the ocean. A few studies have documented annual carbon fluxes in the river, however it is unclear whether floods can create riverine carbon pulses. Such information is critical in understanding the effects that extreme precipitation events may have on carbon transport under the changing climate. We hypothesize that carbon <span class="hlt">concentration</span> and mass loading will increase in response to an increase in river discharge, creating a carbon pulse, and that the source of carbon varies from river rising to falling due to terrestrial runoff processes. This study investigated <span class="hlt">dissolved</span> organic carbon (DOC) and <span class="hlt">dissolved</span> inorganic carbon (DIC) loadings during the 2017 Mississippi River early-summer flood. Water samples were taken from the Mississippi River at Baton Rouge on the rising limb, crest, and falling limb of the flood. All samples were analysed for <span class="hlt">concentrations</span> of DOC, DIC, and their respective isotopic signature (δ13C). Partial pressure of carbon dioxide (pCO2) was also recorded in the field at each sampling trip. Additionally, the water samples were analysed for nutrients, <span class="hlt">dissolved</span> metals, and suspended solids, and in-situ measurements were made on water temperature, pH, <span class="hlt">dissolved</span> oxygen, and specific conductance. The preliminary findings suggest that carbon species responded differently to the flood event and that δ13C values were dependent on river flood stage. This single flood event transported a large quantity of carbon, indicating that frequent large pulses of riverine carbon should be expected in the future as climate change progresses.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1236310-correlation-between-dnapl-distribution-area-dissolved-concentration-surfactant-enhanced-aquifer-remediation-effluent-two-dimensional-flow-cell-study','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1236310-correlation-between-dnapl-distribution-area-dissolved-concentration-surfactant-enhanced-aquifer-remediation-effluent-two-dimensional-flow-cell-study"><span>Correlation between DNAPL distribution area and <span class="hlt">dissolved</span> <span class="hlt">concentration</span> in surfactant enhanced aquifer remediation effluent: a two-dimensional flow cell study</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Wu, Bin; Li, Huiying; Du, Xiaoming</p> <p>2016-02-01</p> <p>During the process of surfactant enhanced aquifer remediation (SEAR), free phase dense non-aqueous phase liquid (DNAPL) may be mobilized and spread. The understanding of the impact of DNAPL spreading on the SEAR remediation is not sufficient with its positive effect infrequently mentioned. To evaluate the correlation between DNAPL spreading and remediation efficiency, a two-dimensional sandbox apparatus was used to simulate the migration and dissolution process of 1,2-DCA (1,2-dichloroethane) DNAPL in SEAR. Distribution area of DNAPL in the sandbox was determined by digital image analysis and correlated with effluent DNAPL <span class="hlt">concentration</span>. The results showed that the effluent DNAPL <span class="hlt">concentration</span> has significantmore » positive linear correlation with the DNAPL distribution area, indicating the mobilization of DNAPL could improve remediation efficiency by enlarging total NAPL-water interfacial area for mass transfer. Meanwhile, the vertical migration of 1,2-DCA was limited within the boundary of aquifer in all experiments, implying that by manipulating injection parameters in SEAR, optimal remediation efficiency can be reached while the risk of DNAPL vertical migration is minimized. This study provides a convenient visible and quantitative method for the optimization of parameters for SEAR project, and an approach of rapid predicting the extent of DNAPL contaminant distribution based on the <span class="hlt">dissolved</span> DNAPL <span class="hlt">concentration</span> in the extraction well.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016JNR....18..259D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016JNR....18..259D"><span>New, rapid method to measure <span class="hlt">dissolved</span> silver <span class="hlt">concentration</span> in silver nanoparticle suspensions by aggregation combined with centrifugation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dong, Feng; Valsami-Jones, Eugenia; Kreft, Jan-Ulrich</p> <p>2016-09-01</p> <p>It is unclear whether the antimicrobial activities of silver nanoparticles (AgNPs) are exclusively mediated by the release of silver ions (Ag+) or, instead, are due to combined nanoparticle and silver ion effects. Therefore, it is essential to quantify <span class="hlt">dissolved</span> Ag in nanosilver suspensions for investigations of nanoparticle toxicity. We developed a method to measure <span class="hlt">dissolved</span> Ag in Ag+/AgNPs mixtures by combining aggregation of AgNPs with centrifugation. We also describe the reproducible synthesis of stable, uncoated AgNPs. Uncoated AgNPs were quickly aggregated by 2 mM Ca2+, forming large clusters that could be sedimented in a low-speed centrifuge. At 20,100g, the sedimentation time of AgNPs was markedly reduced to 30 min due to Ca2+-mediated aggregation, confirmed by the measurements of Ag content in supernatants with graphite furnace atomic absorption spectrometry. No AgNPs were detected in the supernatant by UV-Vis absorption spectra after centrifuging the aggregates. Our approach provides a convenient and inexpensive way to separate <span class="hlt">dissolved</span> Ag from AgNPs, avoiding long ultracentrifugation times or Ag+ adsorption to ultrafiltration membranes.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_20 --> <div id="page_21" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="401"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008JApSc...8..860P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008JApSc...8..860P"><span>Biocidal Efficacy of <span class="hlt">Dissolved</span> Ozone, Formaldehyde and Sodium Hypochlorite Against Total Planktonic Microorganisms in Produced Water</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Puyate, Y. T.; Rim-Rukeh, A.</p> <p></p> <p>The performance of three biocides (<span class="hlt">dissolved</span> ozone, formaldehyde and sodium hypochlorite) in eliminating the bacteria and fungi in produced water is investigated experimentally. The analysis involves monitoring the microbial population in nine conical flasks each containing the same volume of a mixture of produced water, culture medium that sustains the growth of microorganisms and a known <span class="hlt">concentration</span> of biocide. The <span class="hlt">concentrations</span> of each biocide used in the study are 0.1, 0.2 and 0.5 ppm. It is shown that <span class="hlt">dissolved</span> ozone exhibits the best biocidal characteristics and a <span class="hlt">concentration</span> of 0.5 ppm eliminated all the microorganisms in the produced water after 150 min contact time.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20101399','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20101399"><span>The effects of salinity, pH, and <span class="hlt">dissolved</span> organic matter on acute copper toxicity to the rotifer, Brachionus plicatilis ("L" strain).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Arnold, W R; Diamond, R L; Smith, D S</p> <p>2010-08-01</p> <p>This paper presents data from original research for use in the development of a marine biotic ligand model and, ultimately, copper criteria for the protection of estuarine and marine organisms and their uses. Ten 48-h static acute (unfed) copper toxicity tests using the euryhaline rotifer Brachionus plicatilis ("L" strain) were performed to assess the effects of salinity, pH, and <span class="hlt">dissolved</span> organic matter (measured as <span class="hlt">dissolved</span> organic carbon; DOC) on median lethal <span class="hlt">dissolved</span> copper <span class="hlt">concentrations</span> (LC50). Reconstituted and natural saltwater samples were tested at seven salinities (6, 11, 13, 15, 20, 24, and 29 g/L), over a pH range of 6.8-8.6 and a range of <span class="hlt">dissolved</span> organic carbon of <0.5-4.1 mg C/L. Water chemistry analyses (alkalinity, calcium, chloride, DOC, hardness, magnesium, potassium, sodium, salinity, and temperature) are presented for input parameters to the biotic ligand model. In stepwise multiple regression analysis of experimental results where salinity, pH, and DOC <span class="hlt">concentrations</span> varied, copper toxicity was significantly related only to the <span class="hlt">dissolved</span> organic matter content (pH and salinity not statistically retained; alpha=0.05). The relationship of the 48-h <span class="hlt">dissolved</span> copper LC50 values and <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> was LC50 (microg Cu/L)=27.1xDOC (mg C/L)1.25; r2=0.94.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70022587','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70022587"><span>Nitrogen solutes in an Adirondack forested watershed: Importance of <span class="hlt">dissolved</span> organic nitrogen</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>McHale, M.R.; Mitchell, M.J.; McDonnell, Jeffery J.; Cirmo, C.P.</p> <p>2000-01-01</p> <p>Nitrogen (N) dynamics were evaluated from 1 June 1995 through 31 May 1996 within the Arbutus Lake watershed in the Adirondack Mountains of New York State, U.S.A. At the Arbutus Lake outlet <span class="hlt">dissolved</span> organic nitrogen (DON), NO3/- and NH4/+ contributed 61%, 33%, and 6% respectively, to the total <span class="hlt">dissolved</span> nitrogen (TDN) flux (259 mol ha-1 yr-1). At the lake inlet DON, NO3/-, and NH4/+ constituted 36%, 61%, and 3% respectively, of TDN flux (349 mol ha-1 yr-1). Differences between the factors that control DON, NO3/-, and NH4+ stream water <span class="hlt">concentrations</span> were evaluated using two methods for estimating annual N flux at the lake inlet. Using biweekly sampling NO3/- and NH4/+ flux was 10 and 4 mol ha-1 yr-1 respectively, less than flux estimates using biweekly plus storm and snowmelt sampling. DON flux was 18 mol ha-1 yr-1 greater using only biweekly sampling. These differences are probably not of ecological significance relative to the total flux of N from the watershed (349 mol ha-1 yr-1). <span class="hlt">Dissolved</span> organic N <span class="hlt">concentrations</span> were positively related to discharge during both the dormant (R2 = 0.31; P<0.01) and growing season (R2= 0.09; P<0.01). There was no significant relationship between NO3/- <span class="hlt">concentration</span> and discharge during the dormant season, but a significant negative relationship was found during the growing season (R2 = 0.29; P<0.01). Biotic controls in the growing season appeared to have had a larger impact on stream water NO3- <span class="hlt">concentrations</span> than on DON <span class="hlt">concentrations</span>. Arbutus Lake had a major impact on stream water N <span class="hlt">concentrations</span> of the four landscape positions sampled, suggesting the need to quantify within lake processes to interpret N solute losses and patterns in watershed-lake systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29740053','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29740053"><span>A Sixteen-year Decline in <span class="hlt">Dissolved</span> Oxygen in the Central California Current.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ren, Alice S; Chai, Fei; Xue, Huijie; Anderson, David M; Chavez, Francisco P</p> <p>2018-05-08</p> <p>A potential consequence of climate change is global decrease in <span class="hlt">dissolved</span> oxygen at depth in the oceans due to changes in the balance of ventilation, mixing, respiration, and photosynthesis. We present hydrographic cruise observations of declining <span class="hlt">dissolved</span> oxygen collected along CalCOFI Line 66.7 (Line 67) off of Monterey Bay, in the Central California Current region, and investigate likely mechanisms. Between 1998 and 2013, <span class="hlt">dissolved</span> oxygen decreased at the mean rate of 1.92 µmol kg -1 year -1 on σ θ 26.6-26.8 kg m -3 isopycnals (250-400 m), translating to a 40% decline from initial <span class="hlt">concentrations</span>. Two cores of elevated <span class="hlt">dissolved</span> oxygen decline at 130 and 240 km from shore, which we suggest are a California Undercurrent and a California Current signal respectively, occurred on σ θ ranges of 26.0-26.8 kg m -3 (100-400 m). A box model suggests that small annual changes in <span class="hlt">dissolved</span> oxygen in source regions are sufficient to be the primary driver of the mid-depth declines. Variation in <span class="hlt">dissolved</span> oxygen at the bottom of the surface mixed layer suggests that there is also a signal of increased local remineralization.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/ofr/ofr01-089/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/ofr/ofr01-089/"><span>Benthic flux of <span class="hlt">dissolved</span> nickel into the water column of south San Francisco Bay</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Topping, B.R.; Kuwabara, J.S.; Parcheso, Francis; Hager, S.W.; Arnsberg, A.J.; Murphy, Fred</p> <p>2001-01-01</p> <p>Field and laboratory studies were conducted between April, 1998 and May, 1999 to provide the first direct measurements of the benthic flux of <span class="hlt">dissolved</span> (0.2-micron filtered) nickel between the bottom sediment and water column at three sites in the southern component of San Francisco Bay (South Bay), California. <span class="hlt">Dissolved</span> nickel and predominant ligands (represented by <span class="hlt">dissolved</span> organic carbon, and sulfides) were the solutes of primary interest, although a variety of ancillary measurements were also performed to provide a framework for interpretation. Results described herein integrate information needs identified by the State Water Resources Control Board and local stakeholders with fundamental research associated with the U.S. Geological Survey Toxic Substances Hydrology Program. <span class="hlt">Dissolved</span>-Ni <span class="hlt">concentrations</span> in the bottom water over the three sampling dates ranged from 34 to 43 nanomoles per liter. <span class="hlt">Dissolved</span>-macronutrient <span class="hlt">concentrations</span> in the bottom water were consistently higher (frequently by orders of magnitude) than surface-water determinations reported for similar times and locations (Regional Monitoring Program, 2001). This is consistent with measured positive benthic fluxes for the macronutrients. Benthic-flux estimates for <span class="hlt">dissolved</span> nickel from core-incubations, when areally averaged over the South Bay, were significant (that is, of equivalent or greater order of magnitude) relative to previously reported freshwater point and non-point sources. This observation is consistent with previous determinations for other metals, and with the potential remobilization of sediment-associated metals that have been ubiquitously distributed in the South Bay. Similar to <span class="hlt">dissolved</span>-nickel results, benthic flux of macronutrients was also consistently significant relative to surface-water inputs. These results add to a growing body of knowledge that strongly suggests a need to consider contaminant transport across the sediment-water interface when establishing future</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016APS..MARR37012G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016APS..MARR37012G"><span>Flow Meter Based on <span class="hlt">Freely</span> Suspended Smectic Liquid Crystal Films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Green, Adam; Qi, Zhiyuan; Park, Cheol; Glaser, Matthew; Maclennan, Joseph; Clark, Noel</p> <p></p> <p>We present the realization of a idealized 2D hydrodynamic system coupled to air-flow, and show that <span class="hlt">freely</span> suspended films (FSF) of smectic liquid crystals can be used as a novel flow-meter. <span class="hlt">Freely</span>-suspended films of liquid crystals are one of the closest physical realizations of an idealized 2D fluid. The velocity of air-flow above a film suspended above a channel can be inferred by studying the velocity profile of the smectic film. This velocity profile can be measured using digital video microscopy to track the inclusions present in the moving film. The velocity profile is then fitted to the coupled 2D solutions of an embedded fluid in air, and the velocity of the air can then be extracted. This flow meter serves as a demonstration of a robust test-bed for further exploration of 2D hydrodynamics. This work was supported by NASA Grant No. NNX-13AQ81G, NSF MRSEC Grant No. DMR-0820579, and DMR-1420736.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017DSRII.144...92L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017DSRII.144...92L"><span><span class="hlt">Dissolved</span> methane <span class="hlt">concentrations</span> in the water column and surface sediments of Hanna Shoal and Barrow Canyon, Northern Chukchi Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lapham, Laura; Marshall, Kathleen; Magen, Cédric; Lyubchich, Viacheslav; Cooper, Lee W.; Grebmeier, Jacqueline M.</p> <p>2017-10-01</p> <p>Current estimates of methane (CH4) flux suggest that Arctic shelves may be a significant source of atmospheric CH4, a potent greenhouse gas. However, little information is known about the CH4 flux from most Arctic shelves, other than the East Siberian Arctic Shelf. We report here <span class="hlt">dissolved</span> CH4 <span class="hlt">concentrations</span> in the water column and within surface sediments of the Northern Chukchi Sea. We hypothesized that this area contains high <span class="hlt">concentrations</span> of CH4 because it receives nutrient rich waters through the Bering Strait, promoting primary production that enhances an organic-rich material flux to the seafloor and eventual microbial methanogenesis in the sediments. In August 2012, as part of the Chukchi Sea Offshore Monitoring in Drilling Area (COMIDA) project, fourteen stations were sampled on Hanna Shoal, a shallow feature on the shelf, and ten stations across the undersea Barrow Canyon. On Hanna Shoal, water column CH4 <span class="hlt">concentrations</span> ranged from 14 to 74 nM, and surface <span class="hlt">concentrations</span> were up to 15 times supersaturated in CH4 compared to equilibrium with the average atmospheric <span class="hlt">concentrations</span> (3 nM). CH4 <span class="hlt">concentrations</span> at the sediment-water interface were around 1,500 nM, and typically increased with depth in the sediment. At the head of Barrow Canyon, water column CH4 <span class="hlt">concentrations</span> ranged from 5 to 46 nM, with the highest <span class="hlt">concentrations</span> in the deepest waters that were sampled (118 m). Overall, the calculated fluxes to the atmosphere ranged from 1 to 80 μmol CH4 m-2 d-1 for Hanna Shoal and 4 to 17 μmol CH4 m-2 d-1 across the Barrow Canyon stations. Although there was a large range in these fluxes, the average atmospheric flux (20 μmol CH4 m-2 d-1) across Hanna Shoal was 12 times lower than the flux reported from the East Siberian Arctic Shelf in summer. We conclude that while there is a positive flux of CH4 to the atmosphere, this part of the Chukchi Sea is not a significant source of atmospheric CH4 compared to the East Siberian Sea shelf.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70170899','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70170899"><span>Regional-scale controls on <span class="hlt">dissolved</span> nitrous oxide in the Upper Mississippi River</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Turner, P.A.; Griffis, T.J.; Baker, J.M.; Lee, X.; Crawford, John T.; Loken, Luke C.; Venterea, R.T.</p> <p>2016-01-01</p> <p>The U.S. Corn Belt is one of the most intensive agricultural regions of the world and is drained by the Upper Mississippi River (UMR), which forms one of the largest drainage basins in the U.S. While the effects of agricultural nitrate (NO3-) on water quality in the UMR have been well documented, its impact on the production of nitrous oxide (N2O) has not been reported. Using a novel equilibration technique, we present the largest data set of freshwater <span class="hlt">dissolved</span> N2O <span class="hlt">concentrations</span> (0.7 to 6 times saturation) and examine the controls on its variability over a 350 km reach of the UMR. Driven by a supersaturated water column, the UMR was an important atmospheric N2O source (+68 mg N2ONm-2 yr-1) that varies nonlinearly with the NO3-<span class="hlt">concentration</span>. Our analyses indicated that a projected doubling of the NO3-<span class="hlt">concentration</span> by 2050 would cause <span class="hlt">dissolved</span> N2O <span class="hlt">concentrations</span> and emissions to increase by about 40%.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1984/4056/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1984/4056/report.pdf"><span><span class="hlt">Dissolved</span>-oxygen regime of the Jordan River, Salt Lake County, Utah</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Stephens, D.W.</p> <p>1984-01-01</p> <p><span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> oxygen in the Jordan River in Salt Lake County decrease considerably as the river flows northward. Mean <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> oxygen decreased from 8.1 milligrams per liter at the Jordan Narrows to 4.7 milligrams per liter at 500 North Street during April 1981 to September 1982. Coincident with the decrease, the biochemical-oxygen demand increased from 5 to 7 milligrams per liter. About 50 percent of the <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentrations</span> and 90 percent of the 5-day biochemical-oxygen demand measured downstream from 1700 South Street exceeded the State intended-use standards. An estimated 6. million pounds of oxygen-demanding substances as measured by 5-day biochemical-oxygen demand were discharged to the Jordan River during 1981 from point sources downstream from 9000 South Street. Seven wastewater-treatment plants contributed 77 percent of this load, nonstorm base flows contributed 22 percent, and storm flows less than 1 percent. The Surplus Canal diversion at 2100 South Street removed about 70 percent of this load, and travel time of about 1 day also decreased the actual effects of the load on the river. Reaeration rates during September and October were quite high (average K2 at 20 degrees Celsius was about 12 per day) between the Jordan Narrows and 9000 South Street, but they decreased to 2.4 per day in the reach from 1330 South to 1800 North Streets. (USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23505865','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23505865"><span>Nitrogen removal from wastewater and bacterial diversity in activated sludge at different COD/N ratios and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zielińska, Magdalena; Bernat, Katarzyna; Cydzik-Kwiatkowska, Agnieszka; Sobolewska, Joanna; Wojnowska-Baryła, Irena</p> <p>2012-01-01</p> <p>The impact of the organic carbon to nitrogen ratio (chemical oxygen demand (COD)/N) in wastewater and <span class="hlt">dissolved</span> oxygen (DO) <span class="hlt">concentration</span> on carbon and nitrogen removal efficiency, and total bacteria and ammonia-oxidizing bacteria (AOB) communities in activated sludge in constantly aerated sequencing batch reactors (SBRs) was determined. At DO of 0.5 and 1.5 mg O2/L during the aeration phase, the efficiency of ammonia oxidation exceeded 90%, with nitrates as the main product. Nitrification and denitrification achieved under the same operating conditions suggested the simultaneous course of these processes. The most effective nitrogen elimination (above 50%) was obtained at the COD/N ratio of 6.8 and DO of 0.5 mg O2/L. Total bacterial diversity was similar in all experimental series, however, for both COD/N ratios of 6.8 and 0.7, higher values were observed at DO of 0.5 mg O2/L. The diversity and abundance of AOB were higher in the reactors with the COD/N ratio of 0.7 in comparison with the reactors with the COD/N of 6.8. For both COD/N ratios applied, the AOB population was not affected by oxygen <span class="hlt">concentration</span>. Amplicons with sequences indicating membership of the genus Nitrosospira were the determinants of variable technological conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003EAEJA......434U','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003EAEJA......434U"><span>Redox speciation of <span class="hlt">dissolved</span> iron in the northeastern atlantic ocean.</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ussher, S. J.; Achterberg, E. P.; Worsfold, P. J.</p> <p>2003-04-01</p> <p><span class="hlt">Dissolved</span> iron (<0.2 micron) and iron(II) (<0.2 micron) distributions were determined during the Iron from Below and Iron from Above research cruises in the North Eastern Atlantic Ocean. The cruises were part of the EU Ironages project. Iron(II) was measured on-board ship using an iron(II) specific, automated flow injection analyser with luminol chemiluminescence detection [1]. Total <span class="hlt">dissolved</span> iron (DFe) was determined in a land-based laboratory, using the same FI technique but with prior reduction of iron(III) to iron(II) [2]. The limits of detection for the methods were 5 -15 pM and 35 pM respectively, the analysis time was 8 - 10 minutes per sample (minimum of 3 replicates). The Iron from Below expedition took place over the European Continental Shelf, 200 km South West of Brittany (France) in March 2002. A transect between 47.61°N, 4.24°W and 46.00°N, 8.01°W was completed. Over the transect, the depth increased from 100 m to 5000 m. Iron(II) <span class="hlt">concentrations</span> ranged between 10 and 100 pM and DFe between 0.2 and 1 nM, with the higher <span class="hlt">concentrations</span> (Fe(II) ca. > 50 pM and DFe ca. > 0.8 nM) generally found in the shallow shelf waters. These observations imply that benthic inputs and sediment resuspension may form important inputs of <span class="hlt">dissolved</span> iron and iron(II) in the shelf waters. Iron speciation measurements were also made for underway surface and shallow cast samples during the Iron from Above cruise October 2002. Fe(II) and DFe <span class="hlt">concentrations</span> were typically 5 to 50 pM and 0.2 to 0.6 nM, respectively. Sampling was carried out within a grid in the Canary Basin around 5 degrees W of the Canary Islands, an area assumed to be strongly influenced by the Saharan dust plume. Observed Fe(II) <span class="hlt">concentrations</span> are compared and ratioed to the DFe <span class="hlt">concentrations</span>, and indicate that iron(II) forms an important fraction (between 5 and 15%) of the total <span class="hlt">dissolved</span> iron <span class="hlt">concentration</span> in the study areas. Data plots for surface samples are presented with the corresponding physical</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=159408&keyword=oceans+AND+climate+AND+changes&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=159408&keyword=oceans+AND+climate+AND+changes&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span><span class="hlt">DISSOLVED</span> ORGANIC CARBON TRENDS RESULTING FROM CHANGES IN ATMOSPHERIC DEPOSITION CHEMISTRY</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Several hypotheses have been proposed to explain recent, widespread increases in <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic carbon (DOC) in the surface waters of glaciated landscapes across eastern North America and northern and central Europe. Some invoke anthropogenic forcing through ...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016SPIE.9690E..10S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016SPIE.9690E..10S"><span>Chronic monitoring of cortical hemodynamics in behaving, <span class="hlt">freely</span>-moving rats using a miniaturized head-mounted optical microscope</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sigal, Iliya; Gad, Raanan; Koletar, Margaret; Ringuette, Dene; Stefanovic, Bojana; Levi, Ofer</p> <p>2016-03-01</p> <p>Growing interest within the neurophysiology community in assessing healthy and pathological brain activity in animals that are awake and <span class="hlt">freely</span>-behaving has triggered the need for optical systems that are suitable for such longitudinal studies. In this work we report label-free multi-modal imaging of cortical hemodynamics in the somatosensory cortex of awake, <span class="hlt">freely</span>-behaving rats, using a novel head-mounted miniature optical microscope. The microscope employs vertical cavity surface emitting lasers (VCSELs) at three distinct wavelengths (680 nm, 795 nm, and 850 nm) to provide measurements of four hemodynamic markers: blood flow speeds, HbO, HbR, and total Hb <span class="hlt">concentration</span>, across a > 2 mm field of view. Blood flow speeds are extracted using Laser Speckle Contrast Imaging (LSCI), while oxygenation measurements are performed using Intrinsic Optical Signal Imaging (IOSI). Longitudinal measurements on the same animal are made possible over the course of > 6 weeks using a chronic window that is surgically implanted into the skull. We use the device to examine changes in blood flow and blood oxygenation in superficial cortical blood vessels and tissue in response to drug-induced absence-like seizures, correlating motor behavior with changes in blood flow and blood oxygenation in the brain.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26414810','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26414810"><span>Influence of Sulfide Nanoparticles on <span class="hlt">Dissolved</span> Mercury and Zinc Quantification by Diffusive Gradient in Thin-Film Passive Samplers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Pham, Anh Le-Tuan; Johnson, Carol; Manley, Devon; Hsu-Kim, Heileen</p> <p>2015-11-03</p> <p>Diffusive gradient in thin-film (DGT) passive samplers are frequently used to monitor the <span class="hlt">concentrations</span> of metals such as mercury and zinc in sediments and other aquatic environments. The application of these samplers generally presumes that they quantify only the <span class="hlt">dissolved</span> fraction and not particle-bound metal species that are too large to migrate into the sampler. However, metals associated with very small nanoparticles (smaller than the pore size of DGT samplers) can be abundant in certain environments, yet the implications of these nanoparticles for DGT measurements are unclear. The objective of this study was to determine how the performance of the DGT sampler is affected by the presence of nanoparticulate species of Hg and Zn. DGT samplers were exposed to solutions containing known amounts of <span class="hlt">dissolved</span> Hg(II) and nanoparticulate HgS (or <span class="hlt">dissolved</span> Zn(II) and nanoparticulate ZnS). The amounts of Hg and Zn accumulated onto the DGT samplers were quantified over hours to days, and the rates of diffusion of the <span class="hlt">dissolved</span> metal (i.e., the effective diffusion coefficient D) into the sampler's diffusion layer were calculated and compared for solutions containing varying <span class="hlt">concentrations</span> of nanoparticles. The results suggested that the nanoparticles deposited on the surface of the samplers might have acted as sorbents, slowing the migration of the <span class="hlt">dissolved</span> species into the samplers. The consequence was that the DGT sampler data underestimated the <span class="hlt">dissolved</span> metal <span class="hlt">concentration</span> in the solution. In addition, X-ray absorption spectroscopy was employed to determine the speciation of the Hg accumulated on the sampler binding layer, and the results indicated that HgS nanoparticles did not appear to directly contribute to the DGT measurement. Overall, our findings suggest that the deployment of DGT samplers in settings where nanoparticles are relevant (e.g., sediments) may result in DGT data that incorrectly estimated the <span class="hlt">dissolved</span> metal <span class="hlt">concentrations</span>. Models for metal uptake</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11693652','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11693652"><span>Distribution of <span class="hlt">dissolved</span> and labile particulate trace metals in the overlying bottom water in the Vistula River plume (southern Baltic Sea).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Sokolowski, A; Wolowicz, M; Hummel, H</p> <p>2001-10-01</p> <p>Overlying bottom water samples were collected in the Vistula River plume, southern Baltic Sea, (Poland) and analysed for <span class="hlt">dissolved</span> and labile particulate (1 M HCl extractable) Cu, Pb, Zn, Mn, Fe and Ni, hydrological parameters being measured simultaneously. Particulate organic matter (POM), chlorophyll a and <span class="hlt">dissolved</span> oxygen are key factors governing the chemical behaviour of the measured metal fractions. For the <span class="hlt">dissolved</span> Cu, Pb, Zn, Fe and Ni two maxima, in the shallow and in the deeper part of the river plume, were found. In the shallow zone desorption from seaward fluxing metal-rich riverine particles account for markedly increased metal <span class="hlt">concentrations</span>, as confirmed also by high particulate metal contents. For Pb, atmospheric inputs were also considered to have contributed to the elevated <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> Pb adjacent to the river mouth. In the deep zone desorption from detrital and/or resuspended particles by aerobic decomposition of organic material may be the main mechanism responsible for enrichment of particle-reactive metals (Cu, Pb, Zn) in the overyling bottom waters. The increased <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> Fe may have been due to reductive dissolution of Fe oxyhydroxides within the deep sediments by which <span class="hlt">dissolved</span> Ni was released to the water. The distribution of Mn was related to <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>, indicating that Mn is released to the water column under oxygen reduced conditions. However, Mn transfer to the <span class="hlt">dissolved</span> phase from anoxic sediments in deeper part of the Vistula plume was hardly evidenced suggesting that benthic flux of Mn occurs under more severe reductive regime than is consistent with mobilization of Fe. Behaviour of Mn in a shallower part has been presumably affected by release from porewaters and by oxidization into less soluble species resulting in seasonal removal of this metal (e.g. in April) from the <span class="hlt">dissolved</span> phase. The particulate fractions represented from about 6% (Ni) and 33% (Mn, Zn, Cu) to 80% (Fe</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/17450','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/17450"><span>A one-dimensional, steady-state, <span class="hlt">dissolved</span>-oxygen model and waste-load assimilation study for West Fork Blue River, Washington County, Indiana</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Peters, James G.; Wilber, W.G.; Crawford, Charles G.; Girardi, F.P.</p> <p>1979-01-01</p> <p>A digital computer model calibrated to observe stream conditions was used to evaluate water quality in West Fork Blue River, Washington County, IN. Instream <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> averaged 96.5% of saturation at selected sites on West Fork Blue River during two 24-hour summer surveys. This high <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> reflects small carbonaceous and nitrogenous waste loads; adequate dilution of waste by the stream; and natural reaeration. Nonpoint source waste loads accounted for an average of 53.2% of the total carbonaceous biochemical-oxygen demand and 90.2% of the nitrogenous biochemical-oxygen demand. Waste-load assimilation was studiedfor critical summer and winter low flows. Natural streamflow for these conditions was zero, so no benefit from dilution was provided. The projected stream reaeration capacity was not sufficient to maintain the minimum daily <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> (5 milligrams per liter) in the stream with current waste-discharge restrictions. During winter low flow, ammonia toxicity, rather than <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span>, was the limiting water-quality criterion downstream from the Salem wastewater-treatment facility. (USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70189500','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70189500"><span>Relative contributions of copper oxide nanoparticles and <span class="hlt">dissolved</span> copper to Cu uptake kinetics of Gulf killifish (Fundulus grandis) embryos</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Jiang, Chuanjia; Castellon, Benjamin T.; Matson, Cole W.; Aiken, George R.; Hsu-Kim, Heileen</p> <p>2017-01-01</p> <p>The toxicity of soluble metal-based nanomaterials may be due to the uptake of metals in both <span class="hlt">dissolved</span> and nanoparticulate forms, but the relative contributions of these different forms to overall metal uptake rates under environmental conditions are not quantitatively defined. Here, we investigated the linkage between the dissolution rates of copper(II) oxide (CuO) nanoparticles (NPs) and their bioavailability to Gulf killifish (Fundulus grandis) embryos, with the aim of quantitatively delineating the relative contributions of nanoparticulate and <span class="hlt">dissolved</span> species for Cu uptake. Gulf killifish embryos were exposed to <span class="hlt">dissolved</span> Cu and CuO NP mixtures comprising a range of pH values (6.3–7.5) and three types of natural organic matter (NOM) isolates at various <span class="hlt">concentrations</span> (0.1–10 mg-C L–1), resulting in a wide range of CuO NP dissolution rates that subsequently influenced Cu uptake. First-order dissolution rate constants of CuO NPs increased with increasing NOM <span class="hlt">concentration</span> and for NOM isolates with higher aromaticity, as indicated by specific ultraviolet absorbance (SUVA), while Cu uptake rate constants of both <span class="hlt">dissolved</span> Cu and CuO NP decreased with NOM <span class="hlt">concentration</span> and aromaticity. As a result, the relative contribution of <span class="hlt">dissolved</span> Cu and nanoparticulate CuO species for the overall Cu uptake rate was insensitive to NOM type or <span class="hlt">concentration</span> but largely determined by the percentage of CuO that <span class="hlt">dissolved</span>. These findings highlight SUVA and aromaticity as key NOM properties affecting the dissolution kinetics and bioavailability of soluble metal-based nanomaterials in organic-rich waters. These properties could be used in the incorporation of dissolution kinetics into predictive models for environmental risks of nanomaterials.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23219080','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23219080"><span><span class="hlt">Dissolved</span> black carbon in grassland streams: is there an effect of recent fire history?</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ding, Yan; Yamashita, Youhei; Dodds, Walter K; Jaffé, Rudolf</p> <p>2013-03-01</p> <p>While the existence of black carbon as part of <span class="hlt">dissolved</span> organic matter (DOM) has been confirmed, quantitative determinations of <span class="hlt">dissolved</span> black carbon (DBC) in freshwater ecosystem and information on factors controlling its <span class="hlt">concentration</span> are scarce. In this study, stream surface water samples from a series of watersheds subject to different burn frequencies in Konza Prairie (Kansas, USA) were collected in order to determine if recent fire history has a noticeable effect on DBC <span class="hlt">concentration</span>. The DBC levels detected ranged from 0.04 to 0.11 mg L(-1), accounting for ca. 3.32±0.51% of <span class="hlt">dissolved</span> organic carbon (DOC). No correlation was found between DBC <span class="hlt">concentration</span> and neither fire frequency nor time since last burn. We suggest that limited DBC flux is related to high burning efficiency, possibly greater export during periods of high discharge and/or the continuous export of DBC over long time scales. A linear correlation between DOC and DBC <span class="hlt">concentrations</span> was observed, suggesting the export mechanisms determining DOC and DBC <span class="hlt">concentrations</span> are likely coupled. The potential influence of fire history was less than the influence of other factors controlling the DOC and DBC dynamics in this ecosystem. Assuming similar conditions and processes apply in grasslands elsewhere, extrapolation to a global scale would suggest a global grasslands flux of DBC on the order of 0.14 Mt carbon year(-1). Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23893621','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23893621"><span>In vitro immunotoxicology of quantum dots and comparison with <span class="hlt">dissolved</span> cadmium and tellurium.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Bruneau, Audrey; Fortier, Marlene; Gagne, Francois; Gagnon, Christian; Turcotte, Patrice; Tayabali, Azam; Davis, Thomas A; Auffret, Michel; Fournier, Michel</p> <p>2015-01-01</p> <p>The increasing use of products derived from nanotechnology has raised concerns about their potential toxicity, especially at the immunocompetence level in organisms. This study compared the immunotoxicity of cadmium sulfate/cadmium telluride (CdS/Cd-Te) mixture quantum dots (QDs) and their <span class="hlt">dissolved</span> components, cadmium chloride (CdCl2 )/sodium telluride (NaTeO3 ) salts, and a CdCl2 /NaTeO3 mixture on four animal models commonly used in risk assessment studies: one bivalve (Mytilus edulis), one fish (Oncorhynchus mykiss), and two mammals (mice and humans). Our results of viability and phagocytosis biomarkers revealed that QDs were more toxic than <span class="hlt">dissolved</span> metals for blue mussels. For other species, <span class="hlt">dissolved</span> metals (Cd, Te, and Cd-Te mixture) were more toxic than the nanoparticles (NPs). The most sensitive species toward QDs, according to innate immune cells, was humans (inhibitory <span class="hlt">concentration</span> [IC50 ] = 217 μg/mL). However, for adaptative immunity, lymphoblastic transformation in mice was decreased for small QD <span class="hlt">concentrations</span> (EC50 = 4 μg/mL), and was more sensitive than other model species tested. Discriminant function analysis revealed that blue mussel hemocytes were able to discriminate the toxicity of QDs, Cd, Te, and Cd-Te mixture (Partial Wilk's λ = 0.021 and p < 0.0001). For rainbow trout and human cells, the immunotoxic effects of QDs were similar to those obtained with the <span class="hlt">dissolved</span> fraction of Cd and Te mixture. For mice, the toxicity of QDs markedly differed from those observed with Cd, Te, and <span class="hlt">dissolved</span> Cd-Te mixture. The results also suggest that aquatic species responded more differently than vertebrates to these compounds. The results lead to the recommendation that mussels and mice were most able to discriminate the effects of Cd-based NPs from the effects of <span class="hlt">dissolved</span> Cd and Te at the immunocompetence level. © 2013 Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70029892','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70029892"><span>Free zinc ion and <span class="hlt">dissolved</span> orthophosphate effects on phytoplankton from Coeur d'Alene Lake, Idaho</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kuwabara, J.S.; Topping, B.R.; Woods, P.F.; Carter, J.L.</p> <p>2007-01-01</p> <p>Coeur d'Alene Lake in northern Idaho is fed by two major rivers: the Coeur d'Alene River from the east and the St. Joe River from the south, with the Spokane River as its outlet to the north. This phosphorus-limited lake has been subjected to decades of mining (primarily for zinc and silver) and other anthropogenic inputs. A 32 full-factorial experimental design was used to examine the interactive effects of free (uncomplexed) zinc ion and <span class="hlt">dissolved</span>-orthophosphate <span class="hlt">concentrations</span> on phytoplankton that were isolated from two sites along a longitudinal zinc-<span class="hlt">concentration</span> gradient in Coeur d'Alene Lake. The two sites displayed different dominant taxa. Chlorella minutissima, a dominant species near the southern St. Joe River inlet, exhibited greater sensitivity to free Zn ions than Asterionella formosa, collected nearer the Coeur d'Alene River mouth with elevated <span class="hlt">dissolved</span>-zinc <span class="hlt">concentrations</span>. Empirical phytoplankton-response models were generated to describe phytoplankton growth in response to remediation strategies in the surrounding watershed. If <span class="hlt">dissolved</span> Zn can be reduced in the water column from >500 nM (i.e., current <span class="hlt">concentrations</span> near and down stream of the Coeur d'Alene River plume) to <3 nM (i.e., <span class="hlt">concentrations</span> near the southern St. Joe River inlet) such that the lake is truly phosphorus limited, management of phosphorus inputs by surrounding communities will ultimately determine the limnologic state of the lake.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_21 --> <div id="page_22" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="421"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2011RScI...82g4302T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2011RScI...82g4302T"><span>Instrumentation for fast-scan cyclic voltammetry combined with electrophysiology for behavioral experiments in <span class="hlt">freely</span> moving animals</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Takmakov, Pavel; McKinney, Collin J.; Carelli, Regina M.; Wightman, R. Mark</p> <p>2011-07-01</p> <p>Fast-scan cyclic voltammetry is a unique technique for sampling dopamine <span class="hlt">concentration</span> in the brain of rodents in vivo in real time. The combination of in vivo voltammetry with single-unit electrophysiological recording from the same microelectrode has proved to be useful in studying the relationship between animal behavior, dopamine release and unit activity. The instrumentation for these experiments described here has two unique features. First, a 2-electrode arrangement implemented for voltammetric measurements with the grounded reference electrode allows compatibility with electrophysiological measurements, iontophoresis, and multielectrode measurements. Second, we use miniaturized electronic components in the design of a small headstage that can be fixed on the rat's head and used in <span class="hlt">freely</span> moving animals.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3160449','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3160449"><span>Instrumentation for fast-scan cyclic voltammetry combined with electrophysiology for behavioral experiments in <span class="hlt">freely</span> moving animals</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Takmakov, Pavel; McKinney, Collin J.; Carelli, Regina M.; Wightman, R. Mark</p> <p>2011-01-01</p> <p>Fast-scan cyclic voltammetry is a unique technique for sampling dopamine <span class="hlt">concentration</span> in the brain of rodents in vivo in real time. The combination of in vivo voltammetry with single-unit electrophysiological recording from the same microelectrode has proved to be useful in studying the relationship between animal behavior, dopamine release and unit activity. The instrumentation for these experiments described here has two unique features. First, a 2-electrode arrangement implemented for voltammetric measurements with the grounded reference electrode allows compatibility with electrophysiological measurements, iontophoresis, and multielectrode measurements. Second, we use miniaturized electronic components in the design of a small headstage that can be fixed on the rat's head and used in <span class="hlt">freely</span> moving animals. PMID:21806203</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1992JHyd..135..237P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1992JHyd..135..237P"><span><span class="hlt">Dissolved</span> major elements exported by the Congo and the Ubangi rivers during the period 1987 1989</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Probst, Jean-Luc; NKounkou, Renard-Roger; Krempp, Gérard; Bricquet, Jean-Pierre; Thiébaux, Jean-Pierre; Olivry, Jean-Claude</p> <p>1992-07-01</p> <p>On the basis of monthly sampling during the period 1987-1989, the geochemistry of the Congo and the Ubangi (second largest tributary of the Congo) rivers was studied in order (1) to understand the seasonal variations of the physico-chemical parameters of the waters and (2) to estimate the annual <span class="hlt">dissolved</span> fluxes exported by the two rivers. The results presented here correspond to the first three years of measurements carried out for a scientific programme (Interdisciplinary Research Programme on Geodynamics of Peri-Atlantic Intertropical Environments, Operation 'Large River Basins' (PIRAT-GBF) undertaken jointly by Institut National des Sciences de l'Univers (INSU) and Institut Français de Recherche Scientifique pour le Développement en Coopération (ORSTOM) planned to run for at least ten years. The Congo River is more diluted than the Ubangi (34 mgl -1 vs. 42 mgl -1). For both rivers, the inorganic <span class="hlt">dissolved</span> load is composed mainly of HCO 3- and SiO 2. The chemical composition of the water does not change with time. In the Ubangi River, because of the presence of Precambrian carbonate rocks in its catchment, the proportions of HCO 3- and Ca 2+ are higher. On a seasonal scale, the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> cations and anions varies inversely with discharge, except silica. The comparison of the discharge-<span class="hlt">concentration</span> relationship with a theoretical 'zero dilution' shows that the evolution of the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> substances is a simple dilution by the surface waters, with, in the case of the Ubangi, a small supply of <span class="hlt">dissolved</span> substances by the surface waters. Using three different methods of calculation, the estimated annual inorganic <span class="hlt">dissolved</span> flux of the Congo ranges from 39 × 10 6 to 44 × 10 6 tons (according to the year), with about 10% of this coming from the Ubangi drainage basin.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016GeCoA.195....1S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016GeCoA.195....1S"><span><span class="hlt">Dissolved</span> and particulate Barium in the Ganga (Hooghly) River estuary, India: Solute-particle interactions and the enhanced <span class="hlt">dissolved</span> flux to the oceans</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Samanta, Saumik; Dalai, Tarun K.</p> <p>2016-12-01</p> <p>In this study, the sources and the cycling of Ba have been evaluated in the Ganga (Hooghly) River estuary using the composition of the suspended sediments and the water samples collected during six seasons of contrasting water discharge over two years (2012 and 2013). In addition, the data on the samples of groundwater from areas adjacent to the estuary, and the industrial effluent water and urban wastewater draining into the estuary are presented. Selective extraction experiments were also performed on the suspended particulate matter of two seasons to assess the distribution of exchangeable <span class="hlt">concentrations</span> of major ions and Ba. In the mixing zone, the variation patterns of the <span class="hlt">dissolved</span> Ba <span class="hlt">concentrations</span> show mid-salinity maxima and are similar to the patterns of variation of the particulate Mg/Al and Mg/Fe, suggesting that the production of <span class="hlt">dissolved</span> Ba is linked to the adsorption of major ions on to the clay minerals and Fe-Mn oxyhydroxides in the particulate matter. The inference of coupled adsorption-desorption processes is supported by the observations that the particulate Ba/Mg and Ba/K ratios exhibit significant to strong negative correlations with the <span class="hlt">concentrations</span> of Al, Fe and Mn. The observations of mid-salinity maxima for the <span class="hlt">concentrations</span> of exchangeable Mg and K, and of the exchangeable Ba <span class="hlt">concentrations</span> that decrease with salinity provide strong evidence that the solute-particle interactions is the major driver in regulating the <span class="hlt">dissolved</span> Ba distributions in the estuary. The estimates of the quantity of desorbed Ba based on three different approaches suggest that desorption is sufficient to account for the calculated excess Ba (Baxs) <span class="hlt">concentrations</span>. The contribution of Ba to the <span class="hlt">dissolved</span> load via dissolution of the particulate carbonate phases is minor, up to 3% of the maximum Baxs <span class="hlt">concentrations</span>. The estimates of anthropogenic contributions are insignificant, and account for ⩽2% of maximum Baxs in the estuary. Groundwater contributions are</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/7365','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/7365"><span>A one-dimensional, steady-state, <span class="hlt">dissolved</span>-oxygen model and waste-load assimilation study for Cedar Creek, Dekalb and Allen counties, Indiana</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Wilber, William G.; Peters, J.G.; Ayers, M.A.; Crawford, Charles G.</p> <p>1979-01-01</p> <p>A digital model calibrated to conditions in Cedar Creek was used to develop alternatives for future waste loadings that would be compatible with Indiana stream water-quality standards defined for two critical hydrologic conditions, summer and winter low flows. The model indicates that the <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> of the Auburn wastewater effluent and nitrification are the most significant factors affecting the <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> in Cedar Creek during summer low flows. The observed <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> of the Auburn wastewater effluent was low and averaged 30 percent of saturation. Projected nitrogenous biochemical-oxygen demand loads, from the Indiana State Board of Health, for the Auburn and Waterloo wastewater-treatment facilities will result in violations of the current instream <span class="hlt">dissolved</span>-oxygen standard (5 mg/l), even with an effluent <span class="hlt">dissolved</span>-oxygen <span class="hlt">concentration</span> of 80 percent saturation. Natural streamflow for Cedar Creek upstream from the confluence of Willow and Little Cedar Creeks is small compared with the waste discharge, so benefits of dilution for Waterloo and Auburn are minimal. The model also indicates that, during winter low flows, ammonia toxicity, rather than <span class="hlt">dissolved</span> oxygen, is the limiting water-quality criterion in the reach of Cedar Creek downstream from the wastewater-treatment facility at Auburn and the confluence of Garrett ditch. Ammonia-nitrogen <span class="hlt">concentrations</span> predicted for 1978 through 2000 downstream from the Waterloo wastewater-treatment facility do not exceed Indiana water-quality standards for streams. Calculations of the stream 's assimilative capacity indicate that future waste discharge in the Cedar Creek basin will be limited to the reaches between the Auburn wastewater-treatment facility and County Road 68. (Kosco-USGS)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=59961&Lab=NERL&keyword=control+AND+group+AND+experimental&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=59961&Lab=NERL&keyword=control+AND+group+AND+experimental&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>PHOTOCHEMICAL ALTERATION OF <span class="hlt">DISSOLVED</span> ORGANIC MATTER: EFFECTS ON THE <span class="hlt">CONCENTRATION</span> AND ACIDITIES OF IONIZABLE SITES IN <span class="hlt">DISSOLVED</span> ORGANIC MATTER IN THE SATILLA RIVER OF GEORGIA, USA</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>The acid-base properties of humic substances, the major component of <span class="hlt">dissolved</span> organic matter (DOM), area major control on the alkalinity, or acid neutralizing capacity of freshwater systems. Alkalinity is one of the fundamental parameters measured in aquatic sciences, and is an ...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/15044071','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/15044071"><span>Cannabinoids reduce cAMP levels in the striatum of <span class="hlt">freely</span> moving rats: an in vivo microdialysis study.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wade, Mark R; Tzavara, Eleni T; Nomikos, George G</p> <p>2004-04-16</p> <p>The cannabinoid receptor subtype 1 (CB1R) is a member of the G(i)-protein-coupled receptor family and cannabinoid signaling is largely dependent on the suppression of adenylyl cyclase-catalyzed cAMP production. In cell lines transfected with the CB1R or in native tissue preparations, treatment with cannabinoid agonists reduces both basal and forskolin-stimulated cAMP synthesis. We measured extracellular cAMP <span class="hlt">concentrations</span> in the striatum of <span class="hlt">freely</span> moving rats utilizing microdialysis to determine if changes in cAMP <span class="hlt">concentrations</span> in response to CB1R agonists can be monitored in vivo. Striatal infusion of the CB1R agonist WIN55,212-2 (100 microM or 1 mM), dose-dependently decreased basal and forskolin-stimulated extracellular cAMP. These effects were reversed by co-infusion of the CB1R antagonist SR141716A (30 microM), which alone had no effect up to the highest <span class="hlt">concentration</span> tested (300 microM). These data indicate that changes in extracellular cAMP <span class="hlt">concentrations</span> in response to CB1R stimulation can be monitored in vivo allowing the study of cannabinoid signaling in the whole animal.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19673300','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19673300"><span>Characterizing spatial and temporal variability of <span class="hlt">dissolved</span> gases in aquatic environments with in situ mass spectrometry.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Camilli, Richard; Duryea, Anthony N</p> <p>2009-07-01</p> <p>The TETHYS mass spectrometer is intended for long-term in situ observation of <span class="hlt">dissolved</span> gases and volatile organic compounds in aquatic environments. Its design maintains excellent low mass range sensitivity and stability during long-term operations, enabling characterization of low-frequency variability in many trace <span class="hlt">dissolved</span> gases. Results are presented from laboratory trials and a 300-h in situ trial in a shallow marine embayment in Massachusetts, U.S.A. This time series consists of over 15000 sample measurements and represents the longest continuous record made by an in situ mass spectrometer in an aquatic environment. These measurements possess sufficient sampling density and duration to apply frequency analysis techniques for study of temporal variability in <span class="hlt">dissolved</span> gases. Results reveal correlations with specific environmental periodicities. Numerical methods are presented for converting mass spectrometer ion peak ratios to absolute-scale <span class="hlt">dissolved</span> gas <span class="hlt">concentrations</span> across wide temperature regimes irrespective of ambient pressure, during vertical water column profiles in a hypoxic deep marine basin off the coast of California, U.S.A. <span class="hlt">Dissolved</span> oxygen <span class="hlt">concentration</span> values obtained with the TETHYS instrument indicate close correlation with polarographic oxygen sensor data across the entire depth range. These methods and technology enable observation of aquatic environmental chemical distributions and dynamics at appropriate scales of resolution.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23595851','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23595851"><span>Performance of passive samplers for monitoring estuarine water column <span class="hlt">concentrations</span>: 2. Emerging contaminants.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Perron, Monique M; Burgess, Robert M; Suuberg, Eric M; Cantwell, Mark G; Pennell, Kelly G</p> <p>2013-10-01</p> <p>Measuring <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> of emerging contaminants, such as polybrominated diphenyl ethers (PBDEs) and triclosan, can be challenging due to their physicochemical properties resulting in low aqueous solubilities and association with particles. Passive sampling methods have been applied to assess <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> in water and sediments primarily for legacy contaminants. Although the technology is applicable to some emerging contaminants, the use of passive samplers with emerging contaminants is limited. In the present study, the performance of 3 common passive samplers was evaluated for sampling PBDEs and triclosan. Passive sampling polymers included low-density polyethylene (PE) and polyoxymethylene (POM) sheets, and polydimethylsiloxane (PDMS)-coated solid-phase microextraction (SPME) fibers. <span class="hlt">Dissolved</span> <span class="hlt">concentrations</span> were calculated using measured sampler <span class="hlt">concentrations</span> and laboratory-derived partition coefficients. <span class="hlt">Dissolved</span> tri-, tetra-, and pentabrominated PBDE congeners were detected at several of the study sites at very low pg/L <span class="hlt">concentrations</span> using PE and POM. Calculated <span class="hlt">dissolved</span> water <span class="hlt">concentrations</span> of triclosan ranged from 1.7 ng/L to 18 ng/L for POM and 8.8 ng/L to 13 ng/L for PE using performance reference compound equilibrium adjustments. <span class="hlt">Concentrations</span> in SPME were not reported due to lack of detectable chemical in the PDMS polymer deployed. Although both PE and POM were found to effectively accumulate emerging contaminants from the water column, further research is needed to determine their utility as passive sampling devices for emerging contaminants. © 2013 SETAC.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013JNEng..10d6007L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013JNEng..10d6007L"><span>Integrated wireless fast-scan cyclic voltammetry recording and electrical stimulation for reward-predictive learning in awake, <span class="hlt">freely</span> moving rats</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Li, Yu-Ting; Wickens, Jeffery R.; Huang, Yi-Ling; Pan, Wynn H. T.; Chen, Fu-Yu Beverly; Chen, Jia-Jin Jason</p> <p>2013-08-01</p> <p>Objective. Fast-scan cyclic voltammetry (FSCV) is commonly used to monitor phasic dopamine release, which is usually performed using tethered recording and for limited types of animal behavior. It is necessary to design a wireless dopamine sensing system for animal behavior experiments. Approach. This study integrates a wireless FSCV system for monitoring the dopamine signal in the ventral striatum with an electrical stimulator that induces biphasic current to excite dopaminergic neurons in awake <span class="hlt">freely</span> moving rats. The measured dopamine signals are unidirectionally transmitted from the wireless FSCV module to the host unit. To reduce electrical artifacts, an optocoupler and a separate power are applied to isolate the FSCV system and electrical stimulator, which can be activated by an infrared controller. Main results. In the validation test, the wireless backpack system has similar performance in comparison with a conventional wired system and it does not significantly affect the locomotor activity of the rat. In the cocaine administration test, the maximum electrically elicited dopamine signals increased to around 230% of the initial value 20 min after the injection of 10 mg kg-1 cocaine. In a classical conditioning test, the dopamine signal in response to a cue increased to around 60 nM over 50 successive trials while the electrically evoked dopamine <span class="hlt">concentration</span> decreased from about 90 to 50 nM in the maintenance phase. In contrast, the cue-evoked dopamine <span class="hlt">concentration</span> progressively decreased and the electrically evoked dopamine was eliminated during the extinction phase. In the histological evaluation, there was little damage to brain tissue after five months chronic implantation of the stimulating electrode. Significance. We have developed an integrated wireless voltammetry system for measuring dopamine <span class="hlt">concentration</span> and providing electrical stimulation. The developed wireless FSCV system is proven to be a useful experimental tool for the continuous</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23770892','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23770892"><span>Integrated wireless fast-scan cyclic voltammetry recording and electrical stimulation for reward-predictive learning in awake, <span class="hlt">freely</span> moving rats.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Li, Yu-Ting; Wickens, Jeffery R; Huang, Yi-Ling; Pan, Wynn H T; Chen, Fu-Yu Beverly; Chen, Jia-Jin Jason</p> <p>2013-08-01</p> <p>Fast-scan cyclic voltammetry (FSCV) is commonly used to monitor phasic dopamine release, which is usually performed using tethered recording and for limited types of animal behavior. It is necessary to design a wireless dopamine sensing system for animal behavior experiments. This study integrates a wireless FSCV system for monitoring the dopamine signal in the ventral striatum with an electrical stimulator that induces biphasic current to excite dopaminergic neurons in awake <span class="hlt">freely</span> moving rats. The measured dopamine signals are unidirectionally transmitted from the wireless FSCV module to the host unit. To reduce electrical artifacts, an optocoupler and a separate power are applied to isolate the FSCV system and electrical stimulator, which can be activated by an infrared controller. In the validation test, the wireless backpack system has similar performance in comparison with a conventional wired system and it does not significantly affect the locomotor activity of the rat. In the cocaine administration test, the maximum electrically elicited dopamine signals increased to around 230% of the initial value 20 min after the injection of 10 mg kg(-1) cocaine. In a classical conditioning test, the dopamine signal in response to a cue increased to around 60 nM over 50 successive trials while the electrically evoked dopamine <span class="hlt">concentration</span> decreased from about 90 to 50 nM in the maintenance phase. In contrast, the cue-evoked dopamine <span class="hlt">concentration</span> progressively decreased and the electrically evoked dopamine was eliminated during the extinction phase. In the histological evaluation, there was little damage to brain tissue after five months chronic implantation of the stimulating electrode. We have developed an integrated wireless voltammetry system for measuring dopamine <span class="hlt">concentration</span> and providing electrical stimulation. The developed wireless FSCV system is proven to be a useful experimental tool for the continuous monitoring of dopamine levels during animal learning</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1349057-ray-fluorescence-measurements-dissolved-gas-cavitation','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1349057-ray-fluorescence-measurements-dissolved-gas-cavitation"><span>X-ray fluorescence measurements of <span class="hlt">dissolved</span> gas and cavitation</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Duke, Daniel J.; Kastengren, Alan L.; Swantek, Andrew B.; ...</p> <p>2016-09-28</p> <p>The dynamics of <span class="hlt">dissolved</span> gas and cavitation are strongly coupled, yet these phenomena are difficult to measure in-situ. Both create voids in the fluid that can be difficult to distinguish. In this paper, we present an application of X-ray fluorescence in which liquid density and total noncondensible gas <span class="hlt">concentration</span> (both <span class="hlt">dissolved</span> and nucleated) are simultaneously measured. The liquid phase is doped with 400 ppm of a bromine tracer, and <span class="hlt">dissolved</span> air is removed and substituted with krypton. Fluorescent emission at X-ray wavelengths is simultaneously excited from the Br and Kr with a focused monochromatic X-ray beam from a synchrotron source.more » We measure the flow in a cavitating nozzle 0.5 mm in diameter. From Br fluorescence, total displacement of the liquid is measured. From Kr fluorescence, the mass fraction of both <span class="hlt">dissolved</span> and nucleated gas is measured. Volumetric displacement of liquid due to both cavitation and gas precipitation can be separated through estimation of the local equilibrium <span class="hlt">dissolved</span> mass fraction. The uncertainty in the line of sight projected densities of the liquid and gas phases is 4–6 %. The high fluorescence yields and energies of Br and Kr allow small mass fractions of gas to be measured, down to 10 -5, with an uncertainty of 8 %. Finally, these quantitative measurements complement existing optical diagnostic techniques and provide new insight into the diffusion of gas into cavitation bubbles, which can increase their internal density, pressure and lifetimes by orders of magnitude.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=309419&keyword=Polymers&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=309419&keyword=Polymers&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Method 366.0 Determination of <span class="hlt">Dissolved</span> Silicate in Estuarine and Coastal Watersby Gas Segmented Continuous Flow Colorimetric Analysis</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>This method provides a procedure for the determination of <span class="hlt">dissolved</span> silicate <span class="hlt">concentration</span> in estuarine and coastal waters. The <span class="hlt">dissolved</span> silicate is mainly in the form of silicic acid, H SiO , in estuarine and 4 4 coastal waters. All soluble silicate, including colloidal silici...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4555301','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4555301"><span>Seasonal Variation and Sources of <span class="hlt">Dissolved</span> Nutrients in the Yellow River, China</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Gong, Yao; Yu, Zhigang; Yao, Qingzhen; Chen, Hongtao; Mi, Tiezhu; Tan, Jiaqiang</p> <p>2015-01-01</p> <p>The rapid growth of the economy in China has caused dramatic growth in the industrial and agricultural development in the Yellow River (YR) watershed. The hydrology of the YR has changed dramatically due to the climate changes and water management practices, which have resulted in a great variation in the fluxes of riverine nutrients carried by the YR. To study these changes <span class="hlt">dissolved</span> nutrients in the YR were measured monthly at Lijin station in the downstream region of the YR from 2002 to 2004. This study provides detailed information on the nutrient status for the relevant studies in the lower YR and the Bohai Sea. The YR was enriched in nitrate (average 314 μmol·L−1) with a lower <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> silicate (average 131 μmol·L−1) and relatively low <span class="hlt">dissolved</span> phosphate (average 0.35 μmol·L−1). Nutrient <span class="hlt">concentrations</span> exhibited substantial seasonal and yearly variations. The annual fluxes of <span class="hlt">dissolved</span> inorganic nitrogen, phosphate, and silicate in 2004 were 5.3, 2.5, and 4.2 times those in 2002, respectively, primarily due to the increase in river discharge. The relative contributions of nutrient inputs to nitrogen in the YR were: wastewater > fertilizer > atmospheric deposition > soil; while to phosphorus were: wastewater > fertilizer > soil > atmospheric deposition. The ratios of N, P and Si suggest that the YR at Lijin is strongly P-limited with respect to potential phytoplankton growth. PMID:26287226</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2013/5151/pdf/sir2013-5151.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2013/5151/pdf/sir2013-5151.pdf"><span>Groundwater contributions of flow, nitrate, and <span class="hlt">dissolved</span> organic carbon to the lower San Joaquin River, California, 2006-08</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Zamora, Celia; Dahlgren, Randy A.; Kratzer, Charles R.; Downing, Bryan D.; Russell, Ann D.; Dileanis, Peter D.; Bergamaschi, Brian A.; Phillips, Steven P.</p> <p>2013-01-01</p> <p>The influence of groundwater on surface-water quality in the San Joaquin River, California, was examined for a 59-mile reach from the confluence with Salt Slough to Vernalis. The primary objective of this study was to quantify the rate of groundwater discharged to the lower San Joaquin River and the contribution of nitrate and <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> to the river. Multiple lines of evidence from four independent approaches were used to characterize groundwater contributions of nitrogen and <span class="hlt">dissolved</span> organic carbon. Monitoring wells (in-stream and bank wells), streambed synoptic surveys (stream water and shallow groundwater), longitudinal profile surveys by boat (continuous water-quality parameters in the stream), and modeling (MODFLOW and VS2DH) provided a combination of temporal, spatial, quantitative, and qualitative evidence of groundwater contributions to the river and the associated quality. Monitoring wells in nested clusters in the streambed (in-stream wells) and on both banks (bank wells) along the river were monitored monthly from September 2006 to January 2009. Nitrate <span class="hlt">concentrations</span> in the bank wells ranged from less than detection—that is, less than 0.01 milligrams per liter (mg/L) as nitrogen (N)—to approximately 13 mg/L as N. Nitrate was not detected at 17 of 26 monitoring wells during the study period. <span class="hlt">Dissolved</span> organic carbon <span class="hlt">concentrations</span> among monitoring wells were highly variable, but they generally ranged from 1 to 4 mg/L. In a previous study, 14 bank wells were sampled once in 1988 following their original installation. With few exceptions, specific conductivity and nitrate <span class="hlt">concentrations</span> measured in this study were virtually identical to those measured 20 years ago. Streambed synoptic measurements were made by using a temporarily installed drive-point piezometer at 113 distinct transects across the stream during 4 sampling events. Nitrate <span class="hlt">concentrations</span> exceeded the detection limit of 0.01 mg/L as N in 5 percent of</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015E%26PSL.431...87L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015E%26PSL.431...87L"><span><span class="hlt">Dissolved</span> and particulate 230Th-232Th in the Central Equatorial Pacific Ocean: Evidence for far-field transport of the East Pacific Rise hydrothermal plume</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lopez, Grecia I.; Marcantonio, Franco; Lyle, Mitch; Lynch-Stieglitz, Jean</p> <p>2015-12-01</p> <p>We assess the distribution of 230Th and 232Th along a latitudinal gradient in the Central Equatorial Pacific Ocean (∼155°W-159°W) at two sites: 8°N and the equator. The <span class="hlt">dissolved</span> 230Th <span class="hlt">concentration</span> profile at 8°N increases nearly linearly from the surface to 2000 m, exhibiting behavior consistent with thermodynamic reversible scavenging. However, from 2000 m to 3000 m, the <span class="hlt">dissolved</span> 230Th <span class="hlt">concentrations</span> exhibit little change, before increasing slightly from 3000 m to the bottom. At this site <span class="hlt">dissolved</span> 230Th <span class="hlt">concentrations</span> range from 1.1 fg/kg at 100 m to 55.2 fg/kg at 4600 m. At the equator, <span class="hlt">dissolved</span> 230Th <span class="hlt">concentrations</span> are slightly lower, and range from undetectable at 25 m to 19.1 fg/kg at 3038 m. The pattern in the <span class="hlt">dissolved</span> 230Th <span class="hlt">concentration</span> profile at the equator is indistinguishable from that at 8°N. The mid-depth-water deviation from equilibrium reversible scavenging between 2 and 3 km in the 230Th profiles (lower <span class="hlt">concentrations</span> than expected) at both sites occurs in the interval of the water column that is consistent with an interval that has high <span class="hlt">concentrations</span> of 3He and <span class="hlt">dissolved</span> Fe at other nearby sites. This 3He- and Fe-rich signal has been traced to hydrothermal plumes from the East Pacific Rise, thousands of kilometers away. We hypothesize that the lower <span class="hlt">concentrations</span> of 230Th in mid-depth waters of the Central Equatorial Pacific are a result of a 5000-km transit of waters that have had their 230Th scavenged by Fe-Mn particulates close to the EPR. Oceanic residence times of thorium combined with <span class="hlt">dissolved</span> 232Th <span class="hlt">concentrations</span> suggest dust fluxes of about ∼ 0.5- 0.6 gm-2yr-1 to the sea surface. These fluxes are in agreement with other empirical studies in the Pacific, but are higher than those suggested by global atmospheric circulation models.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26ES..121c2012L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26ES..121c2012L"><span>Effect of salinity on the precipitation of <span class="hlt">dissolved</span> metals in the wastewater that produced during fly ash disposal</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lv, Lina; Yang, Yanling; Tian, Junguo; Li, Yaojian; Li, Jun; Yan, Shengjun</p> <p>2018-02-01</p> <p>In this study, a salinity wastewater was produced during the fly ash treatment in the waste incineration plant. Chemical precipitation method was applied for heavy metals removal in the salinity wastewater. The effect of salinity on the removal of <span class="hlt">dissolved</span> heavy metal ions (Zn2+, Cu2+, Pb2+, Ni2+ and Cd2+) was studied, especially on the removal of Pb2+ and Cd2+. Because of the formation of [PbCl3]- and [PbCl4]2- complexes, the residual <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> Pb2+ increased from 0.02 mg/L to 4.08 mg/L, as the NaCl <span class="hlt">concentration</span> increased from 0 % to 10 %. And the residual <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> Cd2+ increased from 0.02 mg/L to 1.39 mg/L, due to the formation of [CdCl3]-, [CdCl4]2- and [CdCl6]4- complexes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/49878','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/49878"><span>Flushing of distal hillslopes as an alternative source of stream <span class="hlt">dissolved</span> organic carbon in a headwater catchment</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>John P. Gannon; Scott W. Bailey; Kevin J. McGuire; James B. Shanley</p> <p>2015-01-01</p> <p>We investigated potential source areas of <span class="hlt">dissolved</span> organic carbon (DOC) in headwater streams by examining DOC <span class="hlt">concentrations</span> in lysimeter, shallow well, and stream water samples from a reference catchment at the Hubbard Brook Experimental Forest. These observations were then compared to high-frequency temporal variations in fluorescent <span class="hlt">dissolved</span> organic matter (FDOM)...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-iss034e031694.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-iss034e031694.html"><span>Hadfield watches a water bubble float <span class="hlt">freely</span> in the Node 1</span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2013-01-21</p> <p>ISS034-E-031694 (21 Jan. 2013) --- Canadian Space Agency astronaut Chris Hadfield, Expedition 34 flight engineer, watches a water bubble float <span class="hlt">freely</span> between him and the camera, showing his image refracted, in the Unity node of the International Space Station.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-iss034e031695.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-iss034e031695.html"><span>Hadfield watches a water bubble float <span class="hlt">freely</span> in the Node 1</span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2013-01-21</p> <p>ISS034-E-031695 (21 Jan. 2013) --- Canadian Space Agency astronaut Chris Hadfield, Expedition 34 flight engineer, watches a water bubble float <span class="hlt">freely</span> between him and the camera, showing his image refracted, in the Unity node of the International Space Station.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_22 --> <div id="page_23" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="441"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSCT44A0204R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSCT44A0204R"><span>Environmental Dynamics of <span class="hlt">Dissolved</span> Black Carbon in the Amazon River</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Roebuck, J. A., Jr.; Gonsior, M.; Enrich-Prast, A.; Jaffe, R.</p> <p>2016-02-01</p> <p><span class="hlt">Dissolve</span> black carbon (DBC) is an important component in the global carbon cycle and constitutes a significant portion of <span class="hlt">dissolved</span> organic carbon (DOC) in aquatic systems. While global fluxes of DBC may be well understood, little is known about systematic processing of this carbon pool in fluvial systems. Similar to DOC, DBC composition may change as it moves throughout a river continuum before it is eventually deposited into the ocean. This is especially important for large river systems that are major sources of DOC to the ocean and may have significant impacts on ocean biogeochemistry and carbon cycling. To better understand variations in DBC dynamics throughout a large fluvial system, DBC was quantified using the benzene polycarboxylic acid method (BPCA) in three major tributaries of the Amazon River, each with varying biogeochemical characteristics. Principal component analysis of the BPCA abundances was used to assess the DBC compositional differences between sampling locations. In some rivers, light availability appeared to influence both DBC quantity and quality. Higher <span class="hlt">concentrations</span> of DBC characterized by a larger, more aromatic DBC pool was found in the Rio Negro, a black water river with high levels of chromophoric <span class="hlt">dissolved</span> organic matter and low light penetration. In the Rio Tapajós, a clear water river with higher light penetration, lower DBC <span class="hlt">concentrations</span> characterized by higher abundances of the less polycondensed DBC pool provided evidence of photodecomposition under such conditions. The Rio Madeira, characterized as a white water river with high suspended sediment yields and high mineral/clay content, had the lowest DBC <span class="hlt">concentrations</span> and the least polycondensed DBC content, suggesting a preferential adsorption of the more highly polycondensed DBC components onto clay particles.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3835161','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3835161"><span>Implantable fiber-optic interface for parallel multisite long-term optical dynamic brain interrogation in <span class="hlt">freely</span> moving mice</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Doronina-Amitonova, L. V.; Fedotov, I. V.; Ivashkina, O. I.; Zots, M. A.; Fedotov, A. B.; Anokhin, K. V.; Zheltikov, A. M.</p> <p>2013-01-01</p> <p>Seeing the big picture of functional responses within large neural networks in a <span class="hlt">freely</span> functioning brain is crucial for understanding the cellular mechanisms behind the higher nervous activity, including the most complex brain functions, such as cognition and memory. As a breakthrough toward meeting this challenge, implantable fiber-optic interfaces integrating advanced optogenetic technologies and cutting-edge fiber-optic solutions have been demonstrated, enabling a long-term optogenetic manipulation of neural circuits in <span class="hlt">freely</span> moving mice. Here, we show that a specifically designed implantable fiber-optic interface provides a powerful tool for parallel long-term optical interrogation of distinctly separate, functionally different sites in the brain of <span class="hlt">freely</span> moving mice. This interface allows the same groups of neurons lying deeply in the brain of a <span class="hlt">freely</span> behaving mouse to be reproducibly accessed and optically interrogated over many weeks, providing a long-term dynamic detection of genome activity in response to a broad variety of pharmacological and physiological stimuli. PMID:24253232</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013NatSR...3E3265D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013NatSR...3E3265D"><span>Implantable fiber-optic interface for parallel multisite long-term optical dynamic brain interrogation in <span class="hlt">freely</span> moving mice</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Doronina-Amitonova, L. V.; Fedotov, I. V.; Ivashkina, O. I.; Zots, M. A.; Fedotov, A. B.; Anokhin, K. V.; Zheltikov, A. M.</p> <p>2013-11-01</p> <p>Seeing the big picture of functional responses within large neural networks in a <span class="hlt">freely</span> functioning brain is crucial for understanding the cellular mechanisms behind the higher nervous activity, including the most complex brain functions, such as cognition and memory. As a breakthrough toward meeting this challenge, implantable fiber-optic interfaces integrating advanced optogenetic technologies and cutting-edge fiber-optic solutions have been demonstrated, enabling a long-term optogenetic manipulation of neural circuits in <span class="hlt">freely</span> moving mice. Here, we show that a specifically designed implantable fiber-optic interface provides a powerful tool for parallel long-term optical interrogation of distinctly separate, functionally different sites in the brain of <span class="hlt">freely</span> moving mice. This interface allows the same groups of neurons lying deeply in the brain of a <span class="hlt">freely</span> behaving mouse to be reproducibly accessed and optically interrogated over many weeks, providing a long-term dynamic detection of genome activity in response to a broad variety of pharmacological and physiological stimuli.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27595700','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27595700"><span>Significance of <span class="hlt">dissolved</span> methane in effluents of anaerobically treated low strength wastewater and potential for recovery as an energy product: A review.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Crone, Brian C; Garland, Jay L; Sorial, George A; Vane, Leland M</p> <p>2016-11-01</p> <p>The need for energy efficient Domestic Wastewater (DWW) treatment is increasing annually with population growth and expanding global energy demand. Anaerobic treatment of low strength DWW produces methane which can be used to as an energy product. Temperature sensitivity, low removal efficiencies (Chemical Oxygen Demand (COD), Suspended Solids (SS), and Nutrients), alkalinity demand, and potential greenhouse gas (GHG) emissions have limited its application to warmer climates. Although well designed anaerobic Membrane Bioreactors (AnMBRs) are able to effectively treat DWW at psychrophilic temperatures (10-30 °C), lower temperatures increase methane solubility leading to increased energy losses in the form of <span class="hlt">dissolved</span> methane in the effluent. Estimates of <span class="hlt">dissolved</span> methane losses are typically based on <span class="hlt">concentrations</span> calculated using Henry's Law but advection limitations can lead to supersaturation of methane between 1.34 and 6.9 times equilibrium <span class="hlt">concentrations</span> and 11-100% of generated methane being lost in the effluent. In well mixed systems such as AnMBRs which use biogas sparging to control membrane fouling, actual <span class="hlt">concentrations</span> approach equilibrium values. Non-porous membranes have been used to recover up to 92.6% of <span class="hlt">dissolved</span> methane and well suited for degassing effluents of Upflow Anaerobic Sludge Blanket (UASB) reactors which have considerable solids and organic contents and can cause pore wetting and clogging in microporous membrane modules. Microporous membranes can recover up to 98.9% of <span class="hlt">dissolved</span> methane in AnMBR effluents which have low COD and SS <span class="hlt">concentrations</span>. Sequential Down-flow Hanging Sponge (DHS) reactors have been used to recover between 57 and 88% of <span class="hlt">dissolved</span> methane from Upflow Anaerobic Sludge Blanket (UASB) reactor effluent at <span class="hlt">concentrations</span> of greater than 30% and oxidize the rest for a 99% removal of total <span class="hlt">dissolved</span> methane. They can also remove 90% of suspended solids and COD in UASB effluents and produce a high quality effluent. In</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1994JThSc...3..191H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1994JThSc...3..191H"><span>Controlling mechanism and resulting spray characteristics of injection of fuel containing <span class="hlt">dissolved</span> gas</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Huang, Zhen; Shao, Yiming; Shiga, Seiichi; Nakamura, Hisao</p> <p>1994-09-01</p> <p>This paper presents a recent advance in the study of injection of fuel containing <span class="hlt">dissolved</span> gas (IFCDG). Using diesel fuel containing <span class="hlt">dissolved</span> CO2, experiments were performed under atmospheric conditions on a diesel hole-type nozzle and simple nozzles. The effects of gas <span class="hlt">concentration</span> in the fuel, injection pressure and the nozzle L/D ratio were examined. In order to reveal the controlling mechanism of IFCDG, the orifice flow pattern, pressure characteristics and their effects were also investigated. The result shows that IFCDG can produce a parabolic-shaped spray pattern with good atomization, which suggests the existence of a new atomization mechanism. In terms of atomization, the beneficial effect of the IFCDG is obtained at the <span class="hlt">dissolved</span> gas <span class="hlt">concentration</span> above the transition and in the region of larger nozzle L/D ratio. However, under unfavorable conditions, IFCDG will lead to deterioration of atomization with coarse fuel droplets. It is found that the big difference of the orifice pressure characteristics caused by the variation of the nozzle L/D ratio has a dominant influence on the separation of the <span class="hlt">dissolved</span> gas from the fuel inside the orifice and is verified to account for a dramatic change in the spray pattern and determine the effect of IFCDG. It is considered that the concept of IFCDG could be attractive in producing more efficient, clean engine and find use in a wide range of application.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFMGC11B0551O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFMGC11B0551O"><span>Chromophoric <span class="hlt">Dissolved</span> Organic Matter in Southwestern Greenland Lakes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Osburn, C. L.; Giles, M. E.; Underwood, G. J. C.</p> <p>2014-12-01</p> <p><span class="hlt">Dissolved</span> organic matter (DOM) is an important property of Arctic lake ecosystems, originating from allochthonous inputs from catchments and autochthonous production by plankton in the water column. Little is known about the quality of DOM in Arctic lakes that lack substantial inputs from catchments and such lakes are abundant in southwestern Greenland. Colored <span class="hlt">dissolved</span> organic matter (CDOM), the fraction that absorbs ultraviolet (UV) and visible light, is the controlling factor for the optical properties of many surface waters and as well informs on the quality of DOM. We examined the quality of CDOM in 21 lakes in southwestern Greenland, from the ice sheet to the coast, as part of a larger study examining the role of DOM in regulating microbial communities in these lakes. DOM was size fractioned and absorbance and fluorescence was measured on each size fraction, as well as on bulk DOM. The specific ultraviolet absorbance (SUVA) at 254 nm (SUVA254), computed by normalizing absorption (a254) to <span class="hlt">dissolved</span> organic carbon (DOC) <span class="hlt">concentration</span>, provided an estimate of the aromatic carbon content of DOM. SUVA values were generally <2, indicating low aromatic content. Parallel factor analysis (PARAFAC) of CDOM fluorescence was used to determine the relative abundance of allochthonous and autochthonous DOM in all size fractions. Younger lakes near the ice sheet and lakes near the coast had lower amounts of CDOM and appeared more microbial in quality. However, lakes centrally located between the ice sheet and the coast had the highest CDOM <span class="hlt">concentrations</span> and exhibited strong humic fluorescence. Overall distinct differences in CDOM quality were observed between lake locations and among DOM size fractions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014EGUGA..16..474K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014EGUGA..16..474K"><span>Direct analysis of δ13C and <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> organic carbon (DOC) in environmental samples by TOC-IRMS</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kirkels, Frédérique; Cerli, Chiara; Federherr, Eugen; Kalbitz, Karsten</p> <p>2014-05-01</p> <p><span class="hlt">Dissolved</span> organic carbon (DOC) plays an important role in carbon cycling in terrestrial and aquatic systems. Stable isotope analysis (delta 13C) of DOC could provide valuable insights in its origin, fluxes and environmental fate. Precise and routine analysis of delta 13C and DOC <span class="hlt">concentration</span> are therefore highly desirable. A promising, new system has been developed for this purpose, linking a high-temperature combustion TOC analyzer trough an interface with a continuous flow isotope ratio mass spectrometer (Elementar group, Hanau, Germany). This TOC-IRMS system enables simultaneous stable isotope (bulk delta 13C) and <span class="hlt">concentration</span> analysis of DOC, with high oxidation efficiency by high-temperature combustion for complex mixtures as natural DOC. To give delta 13C analysis by TOC-IRMS the necessary impulse for broad-scale application, we present a detailed evaluation of its analytical performance for realistic and challenging conditions inclusive low DOC <span class="hlt">concentrations</span> and environmental samples. High precision (standard deviation, SD predominantly < 0.15 permil) and accuracy (R2 = 0.9997, i.e. comparison TOC-IRMS and conventional EA-IRMS) were achieved by TOC-IRMS for a broad diversity of DOC solutions. This precision is comparable or even slightly better than that typically reported for EA-IRMS systems, and improves previous techniques for δ13C analysis of DOC. Simultaneously, very good precision was obtained for DOC <span class="hlt">concentration</span> measurements. Assessment of natural abundance and slightly 13C enriched DOC, a wide range of <span class="hlt">concentrations</span> (0.2-150 mgC/L) and injection volumes (0.05-3 ml), demonstrated good analytical performance with negligible memory effects, no <span class="hlt">concentration</span>/volume effects and a wide linearity. Low DOC <span class="hlt">concentrations</span> (< 2 mgC/L), were correctly analyzed without any pre-<span class="hlt">concentration</span>. Moreover, TOC-IRMS was successfully applied to analyze DOC from diverse terrestrial, freshwater and marine environments (SD < 0.23 permil). In summary, the TOC</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26055751','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26055751"><span>Bisphenol A in Solid Waste Materials, Leachate Water, and Air Particles from Norwegian Waste-Handling Facilities: Presence and Partitioning Behavior.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Morin, Nicolas; Arp, Hans Peter H; Hale, Sarah E</p> <p>2015-07-07</p> <p>The plastic additive bisphenol A (BPA) is commonly found in landfill leachate at levels exceeding acute toxicity benchmarks. To gain insight into the mechanisms controlling BPA emissions from waste and waste-handling facilities, a comprehensive field and laboratory campaign was conducted to quantify BPA in solid waste materials (glass, combustibles, vehicle fluff, waste electric and electronic equipment (WEEE), plastics, fly ash, bottom ash, and digestate), leachate water, and atmospheric dust from Norwegian sorting, incineration, and landfill facilities. Solid waste <span class="hlt">concentrations</span> varied from below 0.002 mg/kg (fly ash) to 188 ± 125 mg/kg (plastics). A novel passive sampling method was developed to, for the first time, establish a set of waste-water partition coefficients, KD,waste, for BPA, and to quantify differences between total and <span class="hlt">freely</span> <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> in waste-facility leachate. Log-normalized KD,waste (L/kg) values were similar for all solid waste materials (from 2.4 to 3.1), excluding glass and metals, indicating BPA is readily leachable. Leachate <span class="hlt">concentrations</span> were similar for landfills and WEEE/vehicle sorting facilities (from 0.7 to 200 μg/L) and dominated by the <span class="hlt">freely</span> <span class="hlt">dissolved</span> fraction, not bound to (plastic) colloids (agreeing with measured KD,waste values). Dust <span class="hlt">concentrations</span> ranged from 2.3 to 50.7 mg/kgdust. Incineration appears to be an effective way to reduce BPA <span class="hlt">concentrations</span> in solid waste, dust, and leachate.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20416946','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20416946"><span>Winter to spring variations of chromophoric <span class="hlt">dissolved</span> organic matter in a temperate estuary (Po River, northern Adriatic Sea).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Berto, D; Giani, M; Savelli, F; Centanni, E; Ferrari, C R; Pavoni, B</p> <p>2010-07-01</p> <p>The light absorbing fraction of <span class="hlt">dissolved</span> organic carbon (DOC), known as chromophoric <span class="hlt">dissolved</span> organic matter (CDOM) showed wide seasonal variations in the temperate estuarine zone in front of the Po River mouth. DOC <span class="hlt">concentrations</span> increased from winter through spring mainly as a seasonal response to increasing phytoplankton production and thermohaline stratification. The monthly dependence of the CDOM light absorption by salinity and chlorophyll a <span class="hlt">concentrations</span> was explored. In 2003, neither DOC nor CDOM were linearly correlated with salinity, due to an exceptionally low Po river inflow. Though the CDOM absorbance coefficients showed a higher content of chromophoric <span class="hlt">dissolved</span> organic matter in 2004 with respect to 2003, the spectroscopic features confirmed that the qualitative nature of CDOM was quite similar in both years. CDOM and DOC underwent a conservative mixing, only after relevant Po river freshets, and a change in optical features with an increase of the specific absorption coefficient was observed, suggesting a prevailing terrestrial origin of <span class="hlt">dissolved</span> organic matter. Published by Elsevier Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29715642','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29715642"><span><span class="hlt">Dissolved</span> Mn(III) in water treatment works: Prevalence and significance.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Johnson, Karen L; McCann, Clare M; Wilkinson, John-Luke; Jones, Matt; Tebo, Bradley M; West, Martin; Elgy, Christine; Clarke, Catherine E; Gowdy, Claire; Hudson-Edwards, Karen A</p> <p>2018-09-01</p> <p><span class="hlt">Dissolved</span> Mn(III) has been identified at all stages throughout a Water Treatment Works (WTW) receiving inflow from a peaty upland catchment in NE England. Ninety percent of the influent total manganese into the WTW is particulate Mn, in the form of Mn oxide (>0.2 μm). Approximately 9% (mean value, n = 22, range of 0-100%) of the <span class="hlt">dissolved</span> (<0.2 μm) influent Mn is present as <span class="hlt">dissolved</span> Mn(III). Mn(III) <span class="hlt">concentrations</span> are highest (mean of 49% of total <span class="hlt">dissolved</span> Mn; n = 26, range of 17-89%) within the WTW where water comes into contact with the organic-rich sludges which are produced as waste products in the WTW. These Mn(III)-containing wastewaters are recirculated to the head of the works and constitute a large input of Mn(III) into the WTW. This is the first report of Mn(III) being identified in a WTW. The ability of Mn(III) to act as both an oxidant and a reductant is of interest to the water industry. Understanding the formation and removal of Mn(III) within may help reduce Mn oxide deposits in pipe networks. Further understanding how the ratio of Mn(III) to Mn(II) can be used to optimise <span class="hlt">dissolved</span> Mn removal would save the water industry significant money in reducing discoloration 'events' at the customers' tap. Copyright © 2018. Published by Elsevier Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3834544','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3834544"><span>Multiple leading edge vortices of unexpected strength in <span class="hlt">freely</span> flying hawkmoth</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Johansson, L. Christoffer; Engel, Sophia; Kelber, Almut; Heerenbrink, Marco Klein; Hedenström, Anders</p> <p>2013-01-01</p> <p>The Leading Edge Vortex (LEV) is a universal mechanism enhancing lift in flying organisms. LEVs, generally illustrated as a single vortex attached to the wing throughout the downstroke, have not been studied quantitatively in <span class="hlt">freely</span> flying insects. Previous findings are either qualitative or from flappers and tethered insects. We measure the flow above the wing of <span class="hlt">freely</span> flying hawkmoths and find multiple simultaneous LEVs of varying strength and structure along the wingspan. At the inner wing there is a single, attached LEV, while at mid wing there are multiple LEVs, and towards the wingtip flow separates. At mid wing the LEV circulation is ~40% higher than in the wake, implying that the circulation unrelated to the LEV may reduce lift. The strong and complex LEV suggests relatively high flight power in hawmoths. The variable LEV structure may result in variable force production, influencing flight control in the animals. PMID:24253180</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20040089721&hterms=opal&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D70%26Ntt%3Dopal','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20040089721&hterms=opal&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D70%26Ntt%3Dopal"><span>Photosynthetic fractionation of 13C and <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> CO2 in the central equatorial Pacific during the last 255,000 years</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Jasper, J. P.; Hayes, J. M.; Mix, A. C.; Prahl, F. G.</p> <p>1994-01-01</p> <p>Carbon isotopically based estimates of CO2 levels have been generated from a record of the photosynthetic fractionation of 13C [is equivalent to epsilon(p)] in a central equatorial Pacific sediment core that spans the last approximately 255 ka. Contents of 13C in phytoplanktonic biomass were determined by analysis of C37 alkadienones. These compounds are exclusive products of Prymnesiophyte algae which at present grow most abundantly at depths of 70-90 m in the central equatorial Pacific. A record of the isotopic composition of <span class="hlt">dissolved</span> CO2 was constructed from isotopic analyses of the planktonic foraminifera Neogloboquadrina dutertrei, which calcifies at 70-90 m in the same region. Values of epsilon(p), derived by comparison of the organic and inorganic delta values, were transformed to yield <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> CO2 [is equivalent to c(e)] based on a new, site-specific calibration of the relationship between epsilon(p) and c(e). The calibration was based on reassessment of existing epsilon(p) versus c(e) data, which support a physiologically based model in which epsilon(p) is inversely related to c(e). Values of PCO2, the partial pressure of CO2 that would be in equilibrium with the estimated <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> CO2, were calculated using Henry's law and the temperature determined from the alkenone-unsaturation index U(K/37). Uncertainties in these values arise mainly from uncertainties about the appropriateness (particularly over time) of the site-specific relationship between epsilon(p) and 1/c(e). These are discussed in detail and it is concluded that the observed record of epsilon(p) most probably reflects significant variations in delta pCO2, the ocean-atmosphere disequilibrium, which appears to have ranged from approximately 110 microatmospheres during glacial intervals (ocean > atmosphere) to approximately 60 microatmospheres during interglacials. Fluxes of CO2 to the atmosphere would thus have been significantly larger during glacial</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29769300','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29769300"><span>Schlieren photography on <span class="hlt">freely</span> flying hawkmoth.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Liu, Yun; Roll, Jesse; Van Kooten, Stephen; Deng, Xinyan</p> <p>2018-05-01</p> <p>The aerodynamic force on flying insects results from the vortical flow structures that vary both spatially and temporally throughout flight. Due to these complexities and the inherent difficulties in studying flying insects in a natural setting, a complete picture of the vortical flow has been difficult to obtain experimentally. In this paper, Schlieren , a widely used technique for highspeed flow visualization, was adapted to capture the vortex structures around <span class="hlt">freely</span> flying hawkmoth ( Manduca ). Flow features such as leading-edge vortex, trailing-edge vortex, as well as the full vortex system in the wake were visualized directly. Quantification of the flow from the Schlieren images was then obtained by applying a physics-based optical flow method, extending the potential applications of the method to further studies of flying insects. © 2018 The Author(s).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26309797','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26309797"><span><span class="hlt">Dissolved</span> Gases and Ice Fracturing During the Freezing of a Multicellular Organism: Lessons from Tardigrades.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kletetschka, Gunther; Hruba, Jolana</p> <p>2015-01-01</p> <p>Three issues are critical for successful cryopreservation of multicellular material: gases <span class="hlt">dissolved</span> in liquid, thermal conductivity of the tissue, and localization of microstructures. Here we show that heat distribution is controlled by the gas amount <span class="hlt">dissolved</span> in liquids and that when changing the liquid into solid, the <span class="hlt">dissolved</span> gases either form bubbles due to the absence of space in the lattice of solids and/or are migrated toward the <span class="hlt">concentrated</span> salt and sugar solution at the cost of amount of heat required to be removed to complete a solid-state transition. These factors affect the heat distribution in the organs to be cryopreserved. We show that the gas <span class="hlt">concentration</span> issue controls fracturing of ice when freezing. There are volumetric changes not only when changing the liquid into solid (volume increases) but also reduction of the volume when reaching lower temperatures (volume decreases). We discuss these issues parallel with observations of the cryosurvivability of multicellular organisms, tardigrades, and discuss their analogy for cryopreservation of large organs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/wri/1993/4085/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/wri/1993/4085/report.pdf"><span>Streamflow, <span class="hlt">dissolved</span> solids, suspended sediment, and trace elements, San Joaquin River, California, June 1985-September 1988</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Hill, B.R.; Gilliom, R.J.</p> <p>1993-01-01</p> <p>The 1985-88 study period included hydrologic extremes throughout most of central California. Except for an 11-month period during and after the 1986 flood, San Joaquin River streamflows during 1985-88 were generally less than median for 1975-88. The Merced Tuolumne, and Stanislaus Rivers together comprised 56 to 69 percent of the annual San Joaquin River flow, Salt and Mud Sloughs together comprised 6 to 19 percent, the upper San Joaquin River comprised 2 to 25 percent, and unmeasured sources from agricultural discharges and ground water accounted for 13 to 20 percent. Salt and Mud Sloughs and the unmeasured sources contribute most of the <span class="hlt">dissolved</span>-solids load. The Merced, Tuolumne, and Stanislaus Rivers greatly dilute <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span>. Suspended-sediment <span class="hlt">concentration</span> peaked sharply at more than 600 milligrams per liter during the flood of February 1986. <span class="hlt">Concentrations</span> and loads varied seasonally during low-flow conditions, with <span class="hlt">concentrations</span> highest during the early summer irrigation season. Trace elements present primarily in <span class="hlt">dissolved</span> phases are arsenic, boron, lithium, molybdenum, and selenium. Boron <span class="hlt">concentrations</span> exceeded the irrigation water-quality criterion of 750 micrograms per liter more than 75 percent of the time in Salt and Mud Sloughs and more than 50 percent of the time at three sites on the San Joaquin River. Selenium <span class="hlt">concentrations</span> exceeded the aquatic-life criterion of 5 micrograms per liter more than 75 percent of the time in Salt Slough and more than 50 percent of the time in Mud Slough and in the San Joaquin River from Salt Slough to the Merced River confluence. <span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> solids, boron, and selenium usually are highest during late winter to early spring, lower in early summer, higher again in mid-to-late summer, and the lowest in autumn, and generally correspond to seasonal inflows of subsurface tile-drain water to Salt and Mud Sloughs. Trace elements present primarily in particulate phases are aluminum</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43F2186B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43F2186B"><span><span class="hlt">Dissolved</span> organic matter in the unsaturated zone: the view from the cave</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Baker, A.; Duan, W.; Rutlidge, H.; McDonough, L.; Oudone, P.; Meredith, K.; Andersen, M. S.; O'Carroll, D. M.; Coleborn, K.; Treble, P. C.</p> <p>2017-12-01</p> <p>Soil organic matter content is typically a few percent of the total soil composition. Diffuse recharge can mobilise some of this soil-derived organic matter. While soil pore water <span class="hlt">dissolved</span> organic matter (DOM) <span class="hlt">concentrations</span> are up to 100 ppm, the resulting groundwater <span class="hlt">dissolved</span> organic matter <span class="hlt">concentration</span> is typically less than 2ppm. <span class="hlt">Dissolved</span> organic matter transported from the soil can be both biodegraded and sorbed to minerals, and the relative importance of these two processes in the unsaturated zone is poorly understood. Caves in karstified limestone uniquely provide direct access to water percolating from the soil to the groundwater. Cave percolation waters can be analysed for their DOM <span class="hlt">concentration</span> and character. This provides insights into the extent and type of biological and chemical processing of DOM during transport from the soil to the groundwater. We determine the <span class="hlt">concentration</span> and characteristics of DOM in cave percolation waters using liquid chromatography (LC-OCD) and optical spectrophotometry (fluorescence and absorbance). We sample DOM from multiple caves in SE Australia (Cathedral Cave, Wellington; South Glory and Harrie Wood Caves, Yarrangobilly), permitting comparison of unsaturated zone DOM properties at different depths (up to 30m below land surface) and different climate zones (montane and temperate). We use caves with long-term hydrological monitoring programs so that DOM in waters of contrasting residence times can be compared. Additionally, we compare these cave percolation water DOM characteristics to those from local and regional groundwater, sampled from nearby wells. Our results will help improve our understanding of how DOM is processed from soil to groundwater, and is also relevant to speleothem scientists interested in using organic matter preserved in speleothems as a paleoclimate or paleoenvironmental proxy.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70034634','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70034634"><span>Toxicity of methylmercury injected into eggs when <span class="hlt">dissolved</span> in water versus corn oil</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Heinz, G.H.; Hoffman, D.J.; Klimstra, J.D.; Stebbins, K.R.; Kondrad, S.L.</p> <p>2011-01-01</p> <p>In a previous study, the embryotoxicity of methylmercury <span class="hlt">dissolved</span> in corn oil was compared among 26 species of birds. Corn oil is not soluble in the water-based matrix that constitutes the albumen of an egg. To determine whether the use of corn oil limited the usefulness of this earlier study, a comparison was made of the embryotoxicity of methylmercury <span class="hlt">dissolved</span> in corn oil versus water. Mallard (Anas platyrhynchos) and chicken (Gallus gallus) eggs were injected with methylmercury chloride <span class="hlt">dissolved</span> in corn oil or water to achieve <span class="hlt">concentrations</span> of 0, 0.2, 0.4, 0.8, and 1.6??g/g mercury in the egg on a wet weight basis. Hatching success at each dose of mercury was compared between the two solvents. For mallards, 16.4% of the eggs injected with 1.6??g/g mercury <span class="hlt">dissolved</span> in water hatched, which was statistically lower than the 37.6% hatch rate of eggs injected with 1.6??g/g mercury <span class="hlt">dissolved</span> in corn oil, but no differences in hatching success were observed between corn oil and water at any of the other doses. With chicken eggs, no significant differences occurred in percentage hatch of eggs between corn oil and water at any of the mercury doses. Methylmercury <span class="hlt">dissolved</span> in corn oil seems to have a toxicity to avian embryos similar to that of does methylmercury <span class="hlt">dissolved</span> in water. Consequently, the results from the earlier study that described the toxicity of methylmercury <span class="hlt">dissolved</span> in corn oil to avian embryos were probably not compromised by the use of corn oil as a solvent. ?? 2011 SETAC.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018WRR....54.2949W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018WRR....54.2949W"><span>Using In-Situ Optical Sensors to Understand the Biogeochemistry of <span class="hlt">Dissolved</span> Organic Matter Across a Stream Network</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wymore, Adam S.; Potter, Jody; Rodríguez-Cardona, Bianca; McDowell, William H.</p> <p>2018-04-01</p> <p>The advent of high-frequency in situ optical sensors provides new opportunities to study the biogeochemistry of <span class="hlt">dissolved</span> organic matter (DOM) in aquatic ecosystems. We used fDOM (fluorescent <span class="hlt">dissolved</span> organic matter) to examine the spatial and temporal variability in <span class="hlt">dissolved</span> organic carbon (DOC) and <span class="hlt">dissolved</span> organic nitrogen (DON) across a heterogeneous stream network that varies in NO3- <span class="hlt">concentration</span>. Across the ten study streams fDOM explained twice the variability in the <span class="hlt">concentration</span> of DOC (r2 = 0.82) compared to DON (r2 = 0.39), which suggests that the N-rich fraction of DOM is either more variable in its sources or more bioreactive than the more stable C-rich fraction. Among sites, DON molar fluorescence was approximately 3x more variable than DOC molar fluorescence and was correlated with changes in inorganic N, indicating that DON is both more variable in composition as well as highly responsive to changes in inorganic N. Laboratory results also indicate that the fDOM sensors we used perform as well as the excitation-emission wavelength pair generally referred to as the "tryptophan-like" peak when measured under laboratory conditions. However, since neither the field sensor not the laboratory measurements explained a large percentage of variation in DON <span class="hlt">concentrations</span>, challenges still remain for monitoring the ambient pool of <span class="hlt">dissolved</span> organic nitrogen. Sensor networks provide new insights into the potential reactivity of DOM and the variability in DOC and DON biogeochemistry across sites. These insights are needed to build spatially explicit models describing organic matter dynamics and water quality.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..1816499R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..1816499R"><span>Catchment scale molecular composition of hydrologically mobilized <span class="hlt">dissolved</span> organic matter</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Raeke, Julia; Lechtenfeld, Oliver J.; Oosterwoud, Marieke R.; Bornmann, Katrin; Tittel, Jörg; Reemtsma, Thorsten</p> <p>2016-04-01</p> <p>Increasing <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> organic matter (DOM) in rivers of temperate catchments in Europe and North Amerika impose new technical challenges for drinking water production. The driving factors for this decadal increase in DOM <span class="hlt">concentration</span> are not conclusive and changes in annual temperatures, precipitation and atmospheric deposition are intensely discussed. It is known that the majority of DOM is released by few but large hydrologic events, mobilizing DOM from riparian wetlands for export by rivers and streams. The mechanisms of this mobilization and the resulting molecular composition of the released DOM may be used to infer long-term changes in the biogeochemistry of the respective catchment. Event-based samples collected over two years from streams in three temperate catchments in the German mid-range mountains were analyzed after solid-phase extraction of DOM for their molecular composition by ultra-high resolution mass spectrometry (FT-ICR MS). Hydrologic conditions, land use and water chemistry parameters were used to complement the molecular analysis. The molecular composition of the riverine DOM was strongly dependent on the magnitude of the hydrologic events, with unsaturated, oxygen-enriched compounds being preferentially mobilized by large events. This pattern is consistent with an increase in <span class="hlt">dissolved</span> iron and aluminum <span class="hlt">concentrations</span>. In contrast, the relative proportions of nitrogen and sulfur bearing compounds increased with an increased agricultural land use but were less affected by the mobilization events. Co-precipitation experiments with colloidal aluminum showed that unsaturated and oxygen-rich compounds are preferentially removed from the <span class="hlt">dissolved</span> phase. The precipitated compounds thus had similar chemical characteristics as compared to the mobilized DOM from heavy rain events. Radiocarbon analyses also indicated that this precipitated fraction of DOM was of comparably young radiocarbon age. DOM radiocarbon from field samples</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017NatGe..10..360M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017NatGe..10..360M"><span>Microbially driven export of labile organic carbon from the Greenland ice sheet</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Musilova, Michaela; Tranter, Martyn; Wadham, Jemma; Telling, Jon; Tedstone, Andrew; Anesio, Alexandre M.</p> <p>2017-04-01</p> <p>Glaciers and ice sheets are significant sources of <span class="hlt">dissolved</span> organic carbon and nutrients to downstream subglacial and marine ecosystems. Climatically driven increases in glacial runoff are expected to intensify the impact of exported nutrients on local and regional downstream environments. However, the origin and bioreactivity of <span class="hlt">dissolved</span> organic carbon from glacier surfaces are not fully understood. Here, we present simultaneous measurements of gross primary production, community respiration, <span class="hlt">dissolved</span> organic carbon composition and export from different surface habitats of the Greenland ice sheet, throughout the ablation season. We found that microbial production was significantly correlated with the <span class="hlt">concentration</span> of labile <span class="hlt">dissolved</span> organic species in glacier surface meltwater. Further, we determined that <span class="hlt">freely</span> available organic compounds made up 62% of the <span class="hlt">dissolved</span> organic carbon exported from the glacier surface through streams. We therefore conclude that microbial communities are the primary driver for labile <span class="hlt">dissolved</span> organic carbon production and recycling on glacier surfaces, and that glacier <span class="hlt">dissolved</span> organic carbon export is dependent on active microbial processes during the melt season.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_23 --> <div id="page_24" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="461"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23228452','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23228452"><span>In situ measurements of <span class="hlt">dissolved</span> oxygen, pH and redox potential of biocathode microenvironments using microelectrodes.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Zejie; Deng, Huan; Chen, Lihui; Xiao, Yong; Zhao, Feng</p> <p>2013-03-01</p> <p>Biofilms are the core component of bioelectrochemical systems (BESs). To understand the polarization effects on biocathode performance of BES, <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span>, pHs and oxidation-reduction potentials of biofilm microenvironments were determined in situ. The results showed that lower polarization potentials resulted in the generation of larger currents and higher pH values, as well as the consumption of more oxygen. Oxidation-reduction potentials of biofilms were mainly affected by polarization potentials of the electrode rather than the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> oxygen or pH value, and its changes in the potentials corresponded to the electric field distribution of the electrode surface. The results demonstrated that a sufficient supply of <span class="hlt">dissolved</span> oxygen and pH control of the biocathode are necessary to obtain optimal performance of BESs; a lower polarization potential endowed microorganisms with a higher electrochemical activity. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSCT44A0227C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSCT44A0227C"><span>Production of <span class="hlt">Dissolved</span> Organic Matter During Doliolid Feeding</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Castellane, N. J.; Paffenhofer, G. A.; Stubbins, A.</p> <p>2016-02-01</p> <p>The biological carbon pump (BCP) draws carbon dioxide out of the atmosphere and buries it at the seafloor. The efficiency of the BCP is determined in part by the sinking rates of particulate organic carbon (POC) from ocean surface waters. Zooplankton can package POC into fecal pellets with higher sinking rates than their food source (e.g. phytoplankton), increasing the efficiency of the BCP. However, <span class="hlt">dissolved</span> organic carbon (DOC) is also produced as zooplankton ingest and egest food, reducing the efficiency of BCP. The pelagic tunicate Dolioletta gegenbauri (doliolid) is a gelatinous zooplankton found at high <span class="hlt">concentrations</span> in shelf waters, including our study site: the South Atlantic Bight. Doliolids are efficient grazers capable of stripping large quantities of phytoplankton from the water column. To determine the balance between pellet formation and DOC production during feeding, doliolids (6-7 mm gonozooids) were placed in natural seawater amended with a live phytoplankton food source and incubated on a plankton wheel. <span class="hlt">Dissolved</span> organic matter (DOM) released directly to the water as well as the water soluble fraction of pellet organic matter were quantified and optically characterized. Colored <span class="hlt">dissolved</span> organic matter (CDOM) absorbance and fluorescence spectra revealed that doliolid feeding produces DOM with optical properties that are commonly indicative of newly produced, highly biolabile DOM of microbial origin. Based upon these optical characteristics, doliolid-produced DOM is expected to be highly bio-labile in the environment and therefore rapidly degraded by surface ocean microbes shunting phytoplankton-derived organic carbon out of the BCP and back to <span class="hlt">dissolved</span> inorganic carbon.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=61347&Lab=NHEERL&keyword=CP&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=61347&Lab=NHEERL&keyword=CP&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>ELEVATED <span class="hlt">DISSOLVED</span> SULFIDES IN SURFICIAL SEDIMENTS OF YAQUINA BAY ESTUARY, OREGON</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p><span class="hlt">Dissolved</span> sulfide <span class="hlt">concentrations</span> were measured in porewater of surficial sediments collected from two exposed intertidal sites in Yaquina Bay, Oregon. Idaho Pt. (IP) is an area where drift green macroalgae is known to accumulate, and the odor of hydrogen sulfide gas (H2S) on th...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA265912','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA265912"><span>VLF Source Localization with a <span class="hlt">Freely</span> Drifting Sensor Array</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>1992-09-01</p> <p>Simultaneous Measurement of Infra - sonic Acoustic Particle Velocity and Acoustic Pressure in the Ocean by F-ely Drifting Swallow Floats," IEEEJ. Ocean. Eng., vol...Pacific. Marine Physical Laboratory’s set of nine <span class="hlt">freely</span> drifting, infrasonic sensors, capable of recording ocean ambient noise in the 1- to 25-Hz range...Terms. 15. Number of Pages, Swallow float, matched-field processing, infrasonic sensor, vlf source localization 153 16. Price Code. 17. Seorlity</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/12557316','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/12557316"><span>Integrated optical sensing of <span class="hlt">dissolved</span> oxygen in microtiter plates: a novel tool for microbial cultivation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>John, Gernot T; Klimant, Ingo; Wittmann, Christoph; Heinzle, Elmar</p> <p>2003-03-30</p> <p>Microtiter plates with integrated optical sensing of <span class="hlt">dissolved</span> oxygen were developed by immobilization of two fluorophores at the bottom of 96-well polystyrene microtiter plates. The oxygen-sensitive fluorophore responded to <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span>, whereas the oxygen-insensitive one served as an internal reference. The sensor measured <span class="hlt">dissolved</span> oxygen accurately in optically well-defined media. Oxygen transfer coefficients, k(L)a, were determined by a dynamic method in a commercial microtiter plate reader with an integrated shaker. For this purpose, the <span class="hlt">dissolved</span> oxygen was initially depleted by the addition of sodium dithionite and, by oxygen transfer from air, it increased again after complete oxidation of dithionite. k(L)a values in one commercial reader were about 10 to 40 h(-1). k(L)a values were inversely proportional to the filling volume and increased with increasing shaking intensity. <span class="hlt">Dissolved</span> oxygen was monitored during cultivation of Corynebacterium glutamicum in another reader that allowed much higher shaking intensity. Growth rates determined from optical density measurement were identical to those observed in shaking flasks and in a stirred fermentor. Oxygen uptake rates measured in the stirred fermentor and <span class="hlt">dissolved</span> oxygen <span class="hlt">concentrations</span> measured during cultivation in the microtiter plate were used to estimate k(L)a values in a 96-well microtiter plate. The resulting values were about 130 h(-1), which is in the lower range of typical stirred fermentors. The resulting maximum oxygen transfer rate was 26 mM h(-1). Simulations showed that the errors caused by the intermittent measurement method were insignificant under the prevailing conditions. Copyright 2003 Wiley Periodicals, Inc. Biotechnol Bioeng 81: 829-836, 2003.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018FrEaS...6...31F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018FrEaS...6...31F"><span><span class="hlt">Dissolved</span> trace and minor elements in cryoconite holes and supraglacial streams, Canada Glacier, Antarctica</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fortner, Sarah K.; Lyons, W. Berry</p> <p>2018-04-01</p> <p>Here we present a synthesis of the trace element chemistry in melt on the surface Canada Glacier, Taylor Valley, McMurdo Dry Valleys (MDV), Antarctica ( 78°S). The MDV is largely ice-free. Low accumulation rates, strong winds, and proximity to the valley floor make these glaciers dusty in comparison to their inland counterparts. This study examines both supraglacial melt streams and cryoconite holes. Supraglacial streams on the lower Canada Glacier have median <span class="hlt">dissolved</span> (<0.4 µm) <span class="hlt">concentrations</span> of Fe, Mn, As, Cu, and V of 71.5, 75.5, 3.7, 4.6, and 4.3 nM. All <span class="hlt">dissolved</span> Cd <span class="hlt">concentrations</span> and the vast majority of Pb values are below our analytical detection (i.e. 0.4 and 0.06 nM). Chemical behavior did not follow similar trends for eastern and western draining waters. Heterogeneity likely reflects distinctions eolian deposition, rock:water ratios, and hydrologic connectivity. Future increases in wind-delivered sediment will likely drive dynamic responses in melt chemistry. For elements above detection limits, <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> in glacier surface melt are within an order of magnitude of <span class="hlt">concentrations</span> observed in proglacial streams (i.e. flowing on the valley floor). This suggests that glacier surfaces are an important source of downstream chemistry. The Fe enrichment of cryoconite water relative to N, P, or Si exceeds enrichment observed in marine phytoplankton. This suggests that the glacier surface is an important source of Fe to downstream ecosystems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23374419','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23374419"><span>Effect of exchangeable cation <span class="hlt">concentration</span> on sorption and desorption of <span class="hlt">dissolved</span> organic carbon in saline soils.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Setia, Raj; Rengasamy, Pichu; Marschner, Petra</p> <p>2013-11-01</p> <p>Sorption is a very important factor in stabilization of <span class="hlt">dissolved</span> organic carbon (DOC) in soils and thus C sequestration. Saline soils have significant potential for C sequestration but little is known about the effect of type and <span class="hlt">concentration</span> of cations on sorption and release of DOC in salt-affected soils. To close this knowledge gap, three batch sorption and desorption experiments were conducted using soils treated with solutions either low or high in salinity. In Experiment 1, salinity was developed with either NaCl or CaCl2 to obtain an electrical conductivity (EC) in a 1:5 soil: water extract (EC1:5) of 2 and 4 dS m(-1). In Experiments 2 and 3, NaCl and CaCl2 were added in various proportions (between 25 and 100%) to obtain an EC1:5 of 0.5 and 4 dS m(-1), respectively. At EC1:5 of 4 dS m(-1), the sorption of DOC (derived from wheat straw) was high even at a low proportion of added Ca(2+) and did not change with proportion of Ca added, but at EC1:5 of 0.5 dS m(-1) increasing proportion of Ca(2+) added increased DOC sorption. This can be explained by the differences in exchangeable Ca(2+) at the two salinity levels. At EC1:5 of 4 dS m(-1), the exchangeable Ca(2+) <span class="hlt">concentration</span> did not increase beyond a proportion of 25% Ca(2+), whereas it increased with increasing Ca(2+) proportion in the treatments at EC1:5 of 0.5 dS m(-1). The DOC sorption was lowest with a proportion of 100% as Na(+). When Ca(2+) was added, DOC sorption was highest, but least was desorbed (with deionised water), thus sorption and desorption of added DOC were inversely related. The results of this study suggest that DOC sorption in salt-affected soils is mainly controlled by the levels of exchangeable Ca(2+) irrespective of the Ca(2+) <span class="hlt">concentration</span> in the soil solution which has implications on carbon stabilization in salt-affected soils. Copyright © 2013 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70035018','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70035018"><span>Ultraviolet absorbance as a proxy for total <span class="hlt">dissolved</span> mercury in streams</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Dittman, J.A.; Shanley, J.B.; Driscoll, C.T.; Aiken, G.R.; Chalmers, A.T.; Towse, J.E.</p> <p>2009-01-01</p> <p>Stream water samples were collected over a range of hydrologic and seasonal conditions at three forested watersheds in the northeastern USA. Samples were analyzed for <span class="hlt">dissolved</span> total mercury (THgd), DOC <span class="hlt">concentration</span> and DOC composition, and UV254 absorbance across the three sites over different seasons and flow conditions. Pooling data from all sites, we found a strong positive correlation of THgd to DOC (r2 = 0.87), but progressively stronger correlations of THgd with the hydrophobic acid fraction (HPOA) of DOC (r2 = 0.91) and with UV254 absorbance (r2 = 0.92). The strength of the UV254 absorbance-THgd relationship suggests that optical properties associated with <span class="hlt">dissolved</span> organic matter may be excellent proxies for THgd <span class="hlt">concentration</span> in these streams. Ease of sample collection and analysis, the potential application of in-situ optical sensors, and the possibility for intensive monitoring over the hydrograph make this an effective, inexpensive approach to estimate THgd flux in drainage waters. ?? 2009 Elsevier Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70185779','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70185779"><span>Associations between benthic flora and diel changes in <span class="hlt">dissolved</span> arsenic, phosphorus, and related physico-chemical parameters</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kuwabara, James S.</p> <p>1992-01-01</p> <p>Diel relationships between physical and chemical parameters and biomass were examined along a 57-km reach of Whitewood Creek, South Dakota, between 29 August and 2 September 1988. A time lag of ∼3-6 h for fluctuations in soluble reactive phosphorus (SRP) <span class="hlt">concentrations</span> (ranging from 0.1 to 0.5 μM at the downstream sites) relative to <span class="hlt">dissolved</span> arsenic (ranging from 0.3 to 1.2 μM as arsenate (pentavalent arsenic)) was consistent with our laboratory studies (reported elsewhere) showing preferential cell sorption of orthophosphate over arsenate by creek periphyton. The potential biological effects on SRP diel fluctuations contrasts with abiotic sorption controls for <span class="hlt">dissolved</span> arsenate (a chemically similar anion). Cycles for pH, like water temperature cycles, lagged irradiance cycles by 1-3 h. Like pH, the amplitude of <span class="hlt">dissolved</span> arsenic diel cycles was greatest at the site with most abundant biomass. Diel fluctuations in specific conductance (an indicator of groundwater inputs at elevated conductivity relative to the water column) were out of phase with both SRP and <span class="hlt">dissolved</span> arsenic <span class="hlt">concentrations</span> suggesting that groundwater was not the direct source of these solutes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28892088','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28892088"><span>Pan-neuronal calcium imaging with cellular resolution in <span class="hlt">freely</span> swimming zebrafish.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kim, Dal Hyung; Kim, Jungsoo; Marques, João C; Grama, Abhinav; Hildebrand, David G C; Gu, Wenchao; Li, Jennifer M; Robson, Drew N</p> <p>2017-11-01</p> <p>Calcium imaging with cellular resolution typically requires an animal to be tethered under a microscope, which substantially restricts the range of behaviors that can be studied. To expand the behavioral repertoire amenable to imaging, we have developed a tracking microscope that enables whole-brain calcium imaging with cellular resolution in <span class="hlt">freely</span> swimming larval zebrafish. This microscope uses infrared imaging to track a target animal in a behavior arena. On the basis of the predicted trajectory of the animal, we applied optimal control theory to a motorized stage system to cancel brain motion in three dimensions. We combined this motion-cancellation system with differential illumination focal filtering, a variant of HiLo microscopy, which enabled us to image the brain of a <span class="hlt">freely</span> swimming larval zebrafish for more than an hour. This work expands the repertoire of natural behaviors that can be studied with cellular-resolution calcium imaging to potentially include spatial navigation, social behavior, feeding and reward.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23493324','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23493324"><span>ChemoPy: <span class="hlt">freely</span> available python package for computational biology and chemoinformatics.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cao, Dong-Sheng; Xu, Qing-Song; Hu, Qian-Nan; Liang, Yi-Zeng</p> <p>2013-04-15</p> <p>Molecular representation for small molecules has been routinely used in QSAR/SAR, virtual screening, database search, ranking, drug ADME/T prediction and other drug discovery processes. To facilitate extensive studies of drug molecules, we developed a <span class="hlt">freely</span> available, open-source python package called chemoinformatics in python (ChemoPy) for calculating the commonly used structural and physicochemical features. It computes 16 drug feature groups composed of 19 descriptors that include 1135 descriptor values. In addition, it provides seven types of molecular fingerprint systems for drug molecules, including topological fingerprints, electro-topological state (E-state) fingerprints, MACCS keys, FP4 keys, atom pairs fingerprints, topological torsion fingerprints and Morgan/circular fingerprints. By applying a semi-empirical quantum chemistry program MOPAC, ChemoPy can also compute a large number of 3D molecular descriptors conveniently. The python package, ChemoPy, is <span class="hlt">freely</span> available via http://code.google.com/p/pychem/downloads/list, and it runs on Linux and MS-Windows. Supplementary data are available at Bioinformatics online.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4686979','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4686979"><span><span class="hlt">Dissolved</span> Organic Carbon Mobilisation in a Groundwater System Stressed by Pumping</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Graham, P. W.; Baker, A.; Andersen, M. S.</p> <p>2015-01-01</p> <p>The <span class="hlt">concentration</span> and flux of organic carbon in aquifers is influenced by recharge and abstraction, and surface and subsurface processing. In this study groundwater was abstracted from a shallow fractured rock aquifer and <span class="hlt">dissolved</span> organic carbon (DOC) was measured in observation bores at different distances from the abstraction bore. Groundwater abstraction at rates exceeding the aquifers yield resulted in increased DOC <span class="hlt">concentration</span> up to 3,500 percent of initial <span class="hlt">concentrations</span>. Potential sources of this increased DOC were determined using optical fluorescence and absorbance analysis. Groundwater fluorescent <span class="hlt">dissolved</span> organic material (FDOM) were found to be a combination of terrestrial-derived humic material and microbial or protein sourced material. Relative molecular weight of FDOM within four metres of the abstraction well increased during the experiment, while the relative molecular weight of FDOM between four and ten metres from the abstraction well decreased. When the aquifer is not being pumped, DOC mobilisation in the aquifer is low. We hypothesise that the physical shear stress on aquifer materials caused by intense abstraction significantly increases the temporary release of DOC from sloughing of biofilms and release of otherwise bound colloidal and sedimentary organic carbon (SOC). PMID:26691238</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22835838','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22835838"><span>Fate of <span class="hlt">dissolved</span> organic nitrogen in two stage trickling filter process.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Simsek, Halis; Kasi, Murthy; Wadhawan, Tanush; Bye, Christopher; Blonigen, Mark; Khan, Eakalak</p> <p>2012-10-15</p> <p><span class="hlt">Dissolved</span> organic nitrogen (DON) represents a significant portion of nitrogen in the final effluent of wastewater treatment plants (WWTPs). Biodegradable portion of DON (BDON) can support algal growth and/or consume <span class="hlt">dissolved</span> oxygen in the receiving waters. The fate of DON and BDON has not been studied for trickling filter WWTPs. DON and BDON data were collected along the treatment train of a WWTP with a two-stage trickling filter process. DON <span class="hlt">concentrations</span> in the influent and effluent were 27% and 14% of total <span class="hlt">dissolved</span> nitrogen (TDN). The plant removed about 62% and 72% of the influent DON and BDON mainly by the trickling filters. The final effluent BDON values averaged 1.8 mg/L. BDON was found to be between 51% and 69% of the DON in raw wastewater and after various treatment units. The fate of DON and BDON through the two-stage trickling filter treatment plant was modeled. The BioWin v3.1 model was successfully applied to simulate ammonia, nitrite, nitrate, TDN, DON and BDON <span class="hlt">concentrations</span> along the treatment train. The maximum growth rates for ammonia oxidizing bacteria (AOB) and nitrite oxidizing bacteria, and AOB half saturation constant influenced ammonia and nitrate output results. Hydrolysis and ammonification rates influenced all of the nitrogen species in the model output, including BDON. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.B43E2170K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.B43E2170K"><span>A multidisciplinary investigation of groundwater fluctuations and their control on river chemistry - Insights from river <span class="hlt">dissolved</span> <span class="hlt">concentrations</span> and Li isotopes during flood events</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kuessner, M.; Bouchez, J.; Dangeard, M.; Bodet, L.; Thiesson, J.; Didon-Lescot, J. F.; Frick, D. A.; Grard, N.; Guérin, R.; Domergue, J. M.; Gaillardet, J.</p> <p>2017-12-01</p> <p>Water flow exerts a strong control on weathering reactions in the Critical Zone (CZ). The relationships between hydrology and river chemistry have been widely studied for the past decades [1]. Solute export responds strongly to storm events [2] and investigating the <span class="hlt">concentration</span> and isotope composition of trace elements in river catchments can advance our understanding of the processes governing water-rock interactions and provide information on the water flow paths during these "hot moments". Especially, lithium (Li) and its isotopes are sensitive to the balance between mineral dissolution and precipitation in the subsurface and therefore, a powerful tool to characterize the response of chemical weathering to hydrology [3]. Hence, high-frequency stream chemistry yields valuable insight into the hydrological processes within the catchment during "hot moments". This study focuses on a CZ Observatory (OHMCV, part of French Research Infrastructure OZCAR). The granitic catchment Sapine (0.54 km2, southern France) is afflicted by big rain events and therefore, it is an appropriate location to study stormflows. Here we combine results from high-frequency stream water sampling during rain events with time-lapse seismic imaging to monitor the changes in aquifer properties [4]. The relationships between <span class="hlt">concentrations</span> and discharge indicate differential responses of <span class="hlt">dissolved</span> elements to the hydrological forcing. Especially, systematic changes are observed for Li and its isotopes as a function of water discharge, suggesting maximum secondary mineral formation at intermediate discharge. We suggest that Li dynamics are chiefly influenced by the depth at which water is flowing with, e.g. dissolution of primary minerals in deeper groundwater flows, and water-secondary mineral interaction at shallower depths. The combination of elemental <span class="hlt">concentrations</span> and Li isotopes in river <span class="hlt">dissolved</span> load tracing chemical weathering, with hydrogeophysical methods mapping water flows and</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70034259','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70034259"><span>The release of <span class="hlt">dissolved</span> nutrients and metals from coastal sediments due to resuspension</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kalnejais, Linda H.; Martin, William R.; Bothner, Michael H.</p> <p>2010-01-01</p> <p>Coastal sediments in many regions are impacted by high levels of contaminants. Due to a combination of shallow water depths, waves, and currents, these sediments are subject to regular episodes of sediment resuspension. However, the influence of such disturbances on sediment chemistry and the release of solutes is poorly understood. The aim of this study is to quantify the release of <span class="hlt">dissolved</span> metals (iron, manganese, silver, copper, and lead) and nutrients due to resuspension in Boston Harbor, Massachusetts, USA. Using a laboratory-based erosion chamber, a range of typical shear stresses was applied to fine-grained Harbor sediments and the solute <span class="hlt">concentration</span> at each shear stress was measured. At low shear stress, below the erosion threshold, limited solutes were released. Beyond the erosion threshold, a release of all solutes, except lead, was observed and the <span class="hlt">concentrations</span> increased with shear stress. The release was greater than could be accounted for by conservative mixing of porewaters into the overlying water, suggesting that sediment resuspension enhances the release of nutrients and metals to the <span class="hlt">dissolved</span> phase. To address the long-term fate of resuspended particles, samples from the erosion chamber were maintained in suspension for 90. h. Over this time, 5-7% of the particulate copper and silver was released to the <span class="hlt">dissolved</span> phase, while manganese was removed from solution. Thus resuspension releases solutes both during erosion events and over a longer timescale due to reactions of suspended particles in the water column. The magnitude of the annual solute release during erosion events was estimated by coupling the erosion chamber results with a record of bottom shear stresses simulated by a hydrodynamic model. The release of <span class="hlt">dissolved</span> copper, lead, and phosphate due to resuspension is between 2% and 10% of the total (<span class="hlt">dissolved</span> plus particulate phase) known inputs to Boston Harbor. Sediment resuspension is responsible for transferring a significant</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFMOS23E1279B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFMOS23E1279B"><span><span class="hlt">Dissolved</span> lead in the deep Southeast Pacific Ocean: results of the 2013 US GEOTRACES cruise</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Boyle, E. A.; Lee, J. M.; Zhang, J.; Echegoyen, Y.</p> <p>2014-12-01</p> <p>Lead (Pb) in the modern ocean is dominated by anthropogenic Pb, which has been evidenced by highly elevated seawater Pb <span class="hlt">concentrations</span> and Pb stable isotope ratios (204Pb, 206Pb, 207Pb, and 208Pb) altered from pre-anthropogenic values. A number of studies have shown the human impact on oceanic Pb in many parts of the world ocean, but little Pb data has been available for the Southeast Pacific Ocean. In this presentation, we will show the <span class="hlt">dissolved</span> Pb (<0.2µm) results from the US GEOTRACES cruise in October - December 2013, which sailed from Manta, Ecuador, to Tahiti along around 12 degrees south. <span class="hlt">Dissolved</span> Pb <span class="hlt">concentrations</span> from all 36 surface stations and deep (>1000m) Pb profiles from 18 stations will be presented, and the results will be also compared to our unpublished data from the BiG RAPA cruise in 2010, whose cruise track from Arica, Peru, to Easter Island is slightly south of the US GEOTRACES cruise. The BiG RAPA data showed that <span class="hlt">dissolved</span> Pb <span class="hlt">concentrations</span> of the southeast Pacific Ocean are relatively low, varying in the range of 8-20 pmol/kg at the surface with a slight maximum (14-22 pmol/kg) at around 400m depth, and 2-10 pmol/kg in deep waters below 1000m depth. The Pb <span class="hlt">concentrations</span> were found to be higher at a marginal station off Peru, reaching 45 pmol/kg at the surface and 65 pmol/kg in the subsurface maximum at 150m depth, and varying between 17 and 23 pmol/kg in deep waters. Our dataset, along with the results from the BiG RAPA cruise, will provide the first overview on the <span class="hlt">dissolved</span> Pb distribution of the southeast Pacific Ocean, which will further our understanding on the human impact on the global ocean.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1087585','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1087585"><span>Relationship between pH and Medium <span class="hlt">Dissolved</span> Solids in Terms of Growth and Metabolism of Lactobacilli and Saccharomyces cerevisiae during Ethanol Production</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Narendranath, Neelakantam V.; Power, Ronan</p> <p>2005-01-01</p> <p>The specific growth rates of four species of lactobacilli decreased linearly with increases in the <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> solids (sugars) in liquid growth medium. This was most likely due to the osmotic stress exerted by the sugars on the bacteria. The reduction in growth rates corresponded to decreased lactic acid production. Medium pH was another factor studied. As the medium pH decreased from 5.5 to 4.0, there was a reduction in the specific growth rate of lactobacilli and a corresponding decrease in the lactic acid produced. In contrast, medium pH did not have any significant effect on the specific growth rate of yeast at any particular <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> solids in the medium. However, medium pH had a significant (P < 0.001) effect on ethanol production. A medium pH of 5.5 resulted in maximal ethanol production in all media with different <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids. When the data were analyzed as a 4 (pH levels) by 4 (<span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> solids) factorial experiment, there was no synergistic effect (P > 0.2923) observed between pH of the medium and <span class="hlt">concentration</span> of <span class="hlt">dissolved</span> solids of the medium in reducing bacterial growth and metabolism. The data suggest that reduction of initial medium pH to 4.0 for the control of lactobacilli during ethanol production is not a good practice as there is a reduction (P < 0.001) in the ethanol produced by the yeast at pH 4.0. Setting the mash (medium) with ≥30% (wt/vol) <span class="hlt">dissolved</span> solids at a pH of 5.0 to 5.5 will minimize the effects of bacterial contamination and maximize ethanol production by yeast. PMID:15870306</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1988DSRA...35..209J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1988DSRA...35..209J"><span>Measures of net oxidant <span class="hlt">concentration</span> in seawater</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Jackson, George A.; Williams, Peter M.</p> <p>1988-02-01</p> <p><span class="hlt">Dissolved</span> oxygen deficits in the ocean have been used as a measure of the organic matter oxidized in a volume of water. Such organic matter is usually assumed to be predominantly settled particles. Using <span class="hlt">dissolved</span> oxygen <span class="hlt">concentration</span> in this way has two problems: first, it does not differentiate between oxidant consumed by the pool of <span class="hlt">dissolved</span> organic matter present near the ocean surface and oxidant consumed by organic matter contained by falling particles; second, it does not account for other oxidant sources, such as nitrate, which can be as important to organic matter decay as oxygen in low-oxygen water, such as off Peru or in the Southern California submarine basins. New parameters provide better measures of the net oxidant <span class="hlt">concentration</span> in a water parcel. One such, NetOx, is changed only by gaseous exchange with the atmosphere, exchange with the benthos, or the production or consumption of sinking particles. A simplified version of NetOx, NetOx = [O2] + 1.25[NO3-] - [TOC], where TOC (total organic carbon), the <span class="hlt">dissolved</span> organic carbon (DOC) plus the suspended particulate organic carbon (POC), provides an index based on the usually dominant variables. Calculation of NetOx and a second property, NetOC ([O2] - [TOC]), for data from GEOSECS and ourselves in the Atlantic and Pacific oceans using property-property graphs show differences from those from oxygen deficits alone. Comparison of NetOx and NetOC <span class="hlt">concentrations</span> at high and low latitudes of the Pacific Ocean shows the difference in surface water oxidant <span class="hlt">concentrations</span> is even larger than the difference in oxygen <span class="hlt">concentration</span>. Vertical particle fluxes off Peru calculated from NetOx gradients are much greater than those calculated from oxygen gradients. The potential value of NetOx and NetOC as parameters to understand particle fluxes implies that determination of TOC should be a routine part of hydrographic measurements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/of/1995/0451/report.pdf','USGSPUBS'); return false;" href="https://pubs.usgs.gov/of/1995/0451/report.pdf"><span><span class="hlt">Dissolved</span> oxygen in the Tualatin River, Oregon, during winter flow conditions, 1991 and 1992</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kelly, V.J.</p> <p>1996-01-01</p> <p>Throughout the winter period, November through April, wastewater treatment plants in the Tualatin River Basin discharge from 10,000 to 15,000 pounds per day of biochemical oxygen demand to the river. These loads often increase substantially during storms when streamflow is high. During the early winter season, when streamflow is frequently less than the average winter flow, the treatment plants discharge about 2,000 pounds per day of ammonia. This study focused on the capacity of the Tualatin River to assimilat oxygen-demanding loads under winter streamflow conditions during the 1992 water year, with an emphasis on peak-flow conditions in the river, and winter-base-flow conditions during November 1992. <span class="hlt">Concentrations</span> of <span class="hlt">dissolved</span> oxygen throughout the main stem of the river during the winter remained generally high relative to the State standard for Oregon of 6 milligrams per liter. The most important factors controlling oxygen consumption during winter-low-flow conditions were carbonaceous biochemical oxygen demand and input of oxygen-depleted waters from tributaries. During peak-flow conditions, reduced travel time and increased dilution associated with the increased streamflow minimized the effect of increased oxygen-demanding loads. During the base-flow period in November 1992, <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> oxygen were consistently below 6 milligrams per liter. A hydrodynamic water-quality model was used to identify the processes depleting <span class="hlt">dissolved</span> oxygen, including sediment oxygen demand, nitrification, and carbonaceous biochemical oxygen demand. Sediment oxygen demand was the most significant factor; nitrification was also important. Hypothetical scenarios were posed to evaluate the effect of different wastewater treatment plant loads during winter-base-flow conditions. Streamflow and temperature were significant factors governing <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> oxygen in the main-stem river.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20582227','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20582227"><span>Spatiotemporal drivers of <span class="hlt">dissolved</span> organic matter in high alpine lakes: Role of Saharan dust inputs and bacterial activity.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mladenov, Natalie; Pulido-Villena, Elvira; Morales-Baquero, Rafael; Ortega-Retuerta, Eva; Sommaruga, Ruben; Reche, Isabel</p> <p>2008-01-01</p> <p>The effects of many environmental stressors such as UV radiation are mediated by <span class="hlt">dissolved</span> organic matter (DOM) properties. Therefore, determining the factors shaping spatial and temporal patterns is particularly essential in the most susceptible, low <span class="hlt">dissolved</span> organic carbon (DOC) lakes. We analyzed spatiotemporal variations in <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentration</span> and <span class="hlt">dissolved</span> organic matter optical properties (absorption and fluorescence) in 11 transparent lakes located above tree line in the Sierra Nevada Mountains (Spain), and we assessed potential external (evaporation and atmospheric deposition) and internal (bacterial abundance, bacterial production, chlorophyll a, and catchment vegetation) drivers of DOM patterns. At spatial and temporal scales, bacteria were related to chromophoric DOM (CDOM). At the temporal scale, water soluble organic carbon (WSOC) in dust deposition and evaporation were found to have a significant influence on DOC and CDOM in two Sierra Nevada lakes studied during the ice-free periods of 2000-2002. DOC <span class="hlt">concentrations</span> and absorption coefficients at 320 nm were strongly correlated over the spatial scale (n = 11, R(2) = 0.86; p < 0.01), but inconsistently correlated over time, indicating seasonal and interannual variability in external factors and a differential response of DOC <span class="hlt">concentration</span> and CDOM to these factors. At the continental scale, higher mean DOC <span class="hlt">concentrations</span> and more CDOM in lakes of the Sierra Nevada than in lakes of the Pyrenees and Alps may be due to a combination of more extreme evaporation, and greater atmospheric dust deposition.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_24 --> <div id="page_25" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="481"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2892303','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2892303"><span>Spatiotemporal drivers of <span class="hlt">dissolved</span> organic matter in high alpine lakes: Role of Saharan dust inputs and bacterial activity</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Mladenov, Natalie; Pulido-Villena, Elvira; Morales-Baquero, Rafael; Ortega-Retuerta, Eva; Sommaruga, Ruben; Reche, Isabel</p> <p>2010-01-01</p> <p>The effects of many environmental stressors such as UV radiation are mediated by <span class="hlt">dissolved</span> organic matter (DOM) properties. Therefore, determining the factors shaping spatial and temporal patterns is particularly essential in the most susceptible, low <span class="hlt">dissolved</span> organic carbon (DOC) lakes. We analyzed spatiotemporal variations in <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentration</span> and <span class="hlt">dissolved</span> organic matter optical properties (absorption and fluorescence) in 11 transparent lakes located above tree line in the Sierra Nevada Mountains (Spain), and we assessed potential external (evaporation and atmospheric deposition) and internal (bacterial abundance, bacterial production, chlorophyll a, and catchment vegetation) drivers of DOM patterns. At spatial and temporal scales, bacteria were related to chromophoric DOM (CDOM). At the temporal scale, water soluble organic carbon (WSOC) in dust deposition and evaporation were found to have a significant influence on DOC and CDOM in two Sierra Nevada lakes studied during the ice-free periods of 2000–2002. DOC <span class="hlt">concentrations</span> and absorption coefficients at 320 nm were strongly correlated over the spatial scale (n = 11, R2 = 0.86; p < 0.01), but inconsistently correlated over time, indicating seasonal and interannual variability in external factors and a differential response of DOC <span class="hlt">concentration</span> and CDOM to these factors. At the continental scale, higher mean DOC <span class="hlt">concentrations</span> and more CDOM in lakes of the Sierra Nevada than in lakes of the Pyrenees and Alps may be due to a combination of more extreme evaporation, and greater atmospheric dust deposition. PMID:20582227</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSCT54A0263O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSCT54A0263O"><span>Optical Proxies for <span class="hlt">Dissolved</span> Organic Matter in Estuaries and Coastal Waters</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Osburn, C. L.; Montgomery, M. T.; Boyd, T. J.; Bianchi, T. S.; Coffin, R. B.; Paerl, H. W.</p> <p>2016-02-01</p> <p>The flux of terrestrial <span class="hlt">dissolved</span> organic carbon (DOC) into the coastal ocean from rivers and estuaries is a major part of the ocean's carbon cycle. Absorbing and fluorescing properties of chromophoric <span class="hlt">dissolved</span> organic matter (CDOM) often are used to fingerprint its sources and to track fluxes of terrestrial DOM into the ocean. They also are used as proxies for organic matter to calibrate remote sensing observations from air and space and from in situ platforms. In general, strong relationships hold for large river dominated estuaries (e.g., the Mississippi River) but little is known about how widely such relationships can be developed in estuaries that have relatively small or multiple riverine inputs. Results are presented from a comparison of six diverse estuarine systems: the Atchafalaya River (ARE), the Mackenzie River (MRE), the Chesapeake Bay (CBE), Charleston Harbor (CHE), Puget Sound (PUG), and the Neuse River (NRE). Mean DOM <span class="hlt">concentrations</span> ranged from 100 to 700 µM and <span class="hlt">dissolved</span> lignin <span class="hlt">concentrations</span> ranged from ca. 3-30 µg L-1. Overall trends were linear between CDOM measured at 350 nm (a350) and DOC <span class="hlt">concentration</span> (R2=0.77) and between a350 and lignin (R2=0.87). Intercepts of a350 vs lignin were not significantly different from zero (P=0.43) suggesting that most of the CDOM was terrestrial in nature. Deviations from these regressions were strongest in the Neuse River Estuary, the most eutrophic of the six estuaries studied. After this calibration procedure, fluorescence modeling via parallel factor analysis (PARAFAC) was used to make estimates of terrigenous and planktonic DOC in these estuaries.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013APS..MARJ28002S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013APS..MARJ28002S"><span>Between soap bubbles and vesicles: The dynamics of <span class="hlt">freely</span> floating smectic bubbles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stannarius, Ralf; May, Kathrin; Harth, Kirsten; Trittel, Torsten</p> <p>2013-03-01</p> <p>The dynamics of droplets and bubbles, particularly on microscopic scales, are of considerable importance in biological, environmental, and technical contexts. We introduce <span class="hlt">freely</span> floating bubbles of smectic liquid crystals and report their unique dynamic properties. Smectic bubbles can be used as simple models for dynamic studies of fluid membranes. In equilibrium, they form minimal surfaces like soap films. However, shape transformations of closed smectic membranes that change the surface area involve the formation and motion of molecular layer dislocations. These processes are slow compared to the capillary wave dynamics, therefore the effective surface tension is zero like in vesicles. <span class="hlt">Freely</span> floating smectic bubbles are prepared from collapsing catenoid films and their dynamics is studied with optical high-speed imaging. Experiments are performed under normal gravity and in microgravity during parabolic flights. Supported by DLR within grant OASIS-Co.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://pubs.water.usgs.gov/sir20045024','USGSPUBS'); return false;" href="http://pubs.water.usgs.gov/sir20045024"><span>Methods to Identify Changes in Background Water-Quality Conditions Using <span class="hlt">Dissolved</span>-Solids <span class="hlt">Concentrations</span> and Loads as Indicators, Arkansas River and Fountain Creek, in the Vicinity of Pueblo, Colorado</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Ortiz, Roderick F.</p> <p>2004-01-01</p> <p>Effective management of existing water-storage capacity in the Arkansas River Basin is anticipated to help satisfy the need for water in southeastern Colorado. A strategy to meet these needs has been developed, but implementation could affect the water quality of the Arkansas River and Fountain Creek in the vicinity of Pueblo, Colorado. Because no known methods are available to determine what effects future changes in operations will have on water quality, the U.S. Geological Survey, in cooperation with the Southeastern Colorado Water Activity Enterprise, began a study in 2002 to develop methods that could identify if future water-quality conditions have changed significantly from background (preexisting) water-quality conditions. A method was developed to identify when significant departures from background (preexisting) water-quality conditions occur in the lower Arkansas River and Fountain Creek in the vicinity of Pueblo, Colorado. Additionally, the methods described in this report provide information that can be used by various water-resource agencies for an internet-based decision-support tool. Estimated <span class="hlt">dissolved</span>-solids <span class="hlt">concentrations</span> at five sites in the study area were evaluated to designate historical background conditions and to calculate tolerance limits used to identify statistical departures from background conditions. This method provided a tool that could be applied with defined statistical probabilities associated with specific tolerance limits. Drought data from 2002 were used to test the method. <span class="hlt">Dissolved</span>-solids <span class="hlt">concentrations</span> exceeded the tolerance limits at all four sites on the Arkansas River at some point during 2002. The number of exceedances was particularly evident when streamflow from Pueblo Reservoir was reduced, and return flows and ground-water influences to the river were more prevalent. No exceedances were observed at the site on Fountain Creek. These comparisons illustrated the need to adjust the <span class="hlt">concentration</span> data to account for</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16955354','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16955354"><span>Supersaturation of <span class="hlt">dissolved</span> H(2) and CO (2) during fermentative hydrogen production with N(2) sparging.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kraemer, Jeremy T; Bagley, David M</p> <p>2006-09-01</p> <p><span class="hlt">Dissolved</span> H(2) and CO(2) were measured by an improved manual headspace-gas chromatographic method during fermentative H(2) production with N(2) sparging. Sparging increased the yield from 1.3 to 1.8 mol H(2)/mol glucose converted, although H(2) and CO(2) were still supersaturated regardless of sparging. The common assumption that sparging increases the H(2) yield because of lower <span class="hlt">dissolved</span> H(2) <span class="hlt">concentrations</span> may be incorrect, because H(2) was not lowered into the range necessary to affect the relevant enzymes. More likely, N(2) sparging decreased the rate of H(2) consumption via lower substrate <span class="hlt">concentrations</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5073323','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5073323"><span>Wireless inertial measurement of head kinematics in <span class="hlt">freely</span>-moving rats</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Pasquet, Matthieu O.; Tihy, Matthieu; Gourgeon, Aurélie; Pompili, Marco N.; Godsil, Bill P.; Léna, Clément; Dugué, Guillaume P.</p> <p>2016-01-01</p> <p>While miniature inertial sensors offer a promising means for precisely detecting, quantifying and classifying animal behaviors, versatile inertial sensing devices adapted for small, <span class="hlt">freely</span>-moving laboratory animals are still lacking. We developed a standalone and cost-effective platform for performing high-rate wireless inertial measurements of head movements in rats. Our system is designed to enable real-time bidirectional communication between the headborne inertial sensing device and third party systems, which can be used for precise data timestamping and low-latency motion-triggered applications. We illustrate the usefulness of our system in diverse experimental situations. We show that our system can be used for precisely quantifying motor responses evoked by external stimuli, for characterizing head kinematics during normal behavior and for monitoring head posture under normal and pathological conditions obtained using unilateral vestibular lesions. We also introduce and validate a novel method for automatically quantifying behavioral freezing during Pavlovian fear conditioning experiments, which offers superior performance in terms of precision, temporal resolution and efficiency. Thus, this system precisely acquires movement information in <span class="hlt">freely</span>-moving animals, and can enable objective and quantitative behavioral scoring methods in a wide variety of experimental situations. PMID:27767085</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5191008','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5191008"><span>A Multi-Pumping Flow System for In Situ Measurements of <span class="hlt">Dissolved</span> Manganese in Aquatic Systems</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Meyer, David; Prien, Ralf D.; Dellwig, Olaf; Waniek, Joanna J.; Schuffenhauer, Ingo; Donath, Jan; Krüger, Siegfried; Pallentin, Malte; Schulz-Bull, Detlef E.</p> <p>2016-01-01</p> <p>A METals In Situ analyzer (METIS) has been used to determine <span class="hlt">dissolved</span> manganese (II) <span class="hlt">concentrations</span> in the subhalocline waters of the Gotland Deep (central Baltic Sea). High-resolution in situ measurements of total <span class="hlt">dissolved</span> Mn were obtained in near real-time by spectrophotometry using 1-(2-pyridylazo)-2-naphthol (PAN). PAN is a complexing agent of <span class="hlt">dissolved</span> Mn and forms a wine-red complex with a maximum absorbance at a wavelength of 562 nm. Results are presented together with ancillary temperature, salinity, and <span class="hlt">dissolved</span> O2 data. Lab calibration of the analyzer was performed in a pressure testing tank. A detection limit of 77 nM was obtained. For validation purposes, discrete water samples were taken by using a pump-CTD system. <span class="hlt">Dissolved</span> Mn in these samples was determined by an independent laboratory based method (inductively coupled plasma–optical emission spectrometry, ICP-OES). Mn measurements from both METIS and ICP-OES analysis were in good agreement. The results showed that the in situ analysis of <span class="hlt">dissolved</span> Mn is a powerful technique reducing dependencies on heavy and expensive equipment (pump-CTD system, ICP-OES) and is also cost and time effective. PMID:27916898</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23863442','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23863442"><span>Accuracy of different sensors for the estimation of pollutant <span class="hlt">concentrations</span> (total suspended solids, total and <span class="hlt">dissolved</span> chemical oxygen demand) in wastewater and stormwater.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lepot, Mathieu; Aubin, Jean-Baptiste; Bertrand-Krajewski, Jean-Luc</p> <p>2013-01-01</p> <p>Many field investigations have used continuous sensors (turbidimeters and/or ultraviolet (UV)-visible spectrophotometers) to estimate with a short time step pollutant <span class="hlt">concentrations</span> in sewer systems. Few, if any, publications compare the performance of various sensors for the same set of samples. Different surrogate sensors (turbidity sensors, UV-visible spectrophotometer, pH meter, conductivity meter and microwave sensor) were tested to link <span class="hlt">concentrations</span> of total suspended solids (TSS), total and <span class="hlt">dissolved</span> chemical oxygen demand (COD), and sensors' outputs. In the combined sewer at the inlet of a wastewater treatment plant, 94 samples were collected during dry weather, 44 samples were collected during wet weather, and 165 samples were collected under both dry and wet weather conditions. From these samples, triplicate standard laboratory analyses were performed and corresponding sensors outputs were recorded. Two outlier detection methods were developed, based, respectively, on the Mahalanobis and Euclidean distances. Several hundred regression models were tested, and the best ones (according to the root mean square error criterion) are presented in order of decreasing performance. No sensor appears as the best one for all three investigated pollutants.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2001AGUFM.H11B0238H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2001AGUFM.H11B0238H"><span>A Comparison of <span class="hlt">Dissolved</span> and Particulate Organic Material in Two Southwestern Desert River Systems</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Haas, P. A.; Brooks, P.</p> <p>2001-12-01</p> <p>Desert river systems of the southwestern U.S. acquire a substantial fraction of their <span class="hlt">dissolved</span> organic matter (DOM) from the terrestrial environment during episodic rain events. This DOM provides carbon for stream metabolism and nitrogen, which is limiting in lower order streams in this environment. The San Pedro and Rio Grande Rivers represent two endpoints of catchment scale, discharge, and land use in the southwest. The San Pedro is a protected riparian corridor (San Pedro Riparian National Conservation Area), while the middle Rio Grande is a large river with extensive agriculture, irrigation, and reservoirs. Relative abundance and spectral properties of fulvic acids isolated from filtered samples were used to determine the source of <span class="hlt">dissolved</span> organic carbon (DOC). Total DOC and particulate organic carbon (POC) changes with respect to episodic flooding events were compared for the two river systems. The San Pedro River DOC <span class="hlt">concentrations</span> remain low approximately 2.2 to 3.3 ppm unless a relatively large storm event occurs when <span class="hlt">concentrations</span> may go above 5.5 ppm (1000cfs flow). In contrast typical <span class="hlt">concentrations</span> for the Rio Grande were approximately 5 ppm during the monsoon season. Particulate organic matter (POM) appears to be a more significant source of organic matter to the San Pedro than DOM. The relative importance of terrestrial vs. aquatic and <span class="hlt">dissolved</span> vs. particulate organic matter with respect to aquatic ecosystems will be discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19758677','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19758677"><span>A three-compartment model for micropollutants sorption in sludge: methodological approach and insights.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Barret, Maialen; Patureau, Dominique; Latrille, Eric; Carrère, Hélène</p> <p>2010-01-01</p> <p>In sludge resulting from wastewater treatment, organic micropollutants sorb to particles and to <span class="hlt">dissolved</span>/colloidal matter (DCM). Both interactions may influence their physical and biological fate throughout the wastewater treatment processes. To our knowledge, sludge has never been considered as a three-compartment matrix, in which micropollutants coexist in three states: <span class="hlt">freely</span> <span class="hlt">dissolved</span>, sorbed-to-particles and sorbed-to-DCM. A methodology is proposed to concomitantly determine equilibrium constants of sorption to particles (K(part)) and to DCM (K(DCM)). Polycyclic Aromatic Hydrocarbons (PAHs) were chosen as model compounds for the experiments. The logarithm of estimated equilibrium constants ranged from 3.1 to 4.3 and their usual correlation to PAH hydrophobicity was verified. Moreover, PAH affinities for particles and for DCM could be compared. Affinity for particles was found to be stronger, probably due to their physical and chemical characteristics. This work provided a useful tool to assess the <span class="hlt">freely</span> <span class="hlt">dissolved</span>, sorbed-to-particles and sorbed-to-DCM <span class="hlt">concentrations</span> of contaminants, which are necessary to accurately predict their fate. Besides, guidelines to investigate the link between sorption and the fundamental concept of bioavailability were proposed. (c) 2009 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B43B0235H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B43B0235H"><span>Characterizing <span class="hlt">dissolved</span> organic carbon <span class="hlt">concentrations</span> and export in a boreal forest-peatland landscape under the influence of rapidly degrading discontinuous permafrost</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hanisch, J.; Connon, R.; Templeton, M.; Quinton, W. L.; Olefeldt, D.; Moore, T. R.; Roulet, N. T.; Sonnentag, O.</p> <p>2014-12-01</p> <p>Our current understanding of peatland energy, water and carbon (C) cycles implies that northern peatlands are vulnerable to projected climate change, and that the perturbation of these cycles might cause a strong positive or negative net feedback to the climate system. About one third of Canada's northern peatlands contain contain perennialy frozen ground (permafrost). Boreal forest-peatland ecosystems in the discontinuous permafrost zone (50-90% of frozen ground) are especially vulnerable to rising temperatures as permafrost is ice-rich, relatively warm and thin, and thus susceptible to complete disappearance causing ground surface subsidence and a decline in forest cover in response to water-logging. Several recent studies have substantially improved our understanding of northern peatland's role in the climate system by quantifying their net ecosystem C balance which includes atmospheric and aqueous C fluxes generally dominated by the export of <span class="hlt">dissolved</span> organic C (DOC). We characterize seasonal and diurnal variations in DOC export from five catchments (0.02-0.05 km2) at Scotty Creek, a 152 km2-watershed under the influence of rapidly degrading and disappearing discontinuous permafrost near Fort Simpson, Northwest Territories, Canada. The five catchments are characterized by different fractions of forested peat plateaus with permafrost (38-73%) and permafrost-free collapse bogs (27-62%). <span class="hlt">Dissolved</span> organic carbon <span class="hlt">concentrations</span> at Scotty Creek appear to be higher in catchments where the percentage of peat plateaus is higher compared to bogs, independent of catchment size. Average DOC <span class="hlt">concentration</span> for catchments with a lower percentage of peat plateaus is lower (~43 mg/l) than for those with a higher percentage of plateaus (~60 mg/l). These preliminary results suggest that lateral C losses from this rapidly changing landscape are at least partly controlled by the peat plateau-bog ratio. Over the year, DOC export from the five catchments is limited to around a week</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2000SPIE.3921..256Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2000SPIE.3921..256Y"><span>External optical imaging of <span class="hlt">freely</span> moving mice with green fluorescent protein-expressing metastatic tumors</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yang, Meng; Baranov, Eugene; Shimada, Hiroshi; Moossa, A. R.; Hoffman, Robert M.</p> <p>2000-04-01</p> <p>We report here a new approach to genetically engineering tumors to become fluorescence such that they can be imaged externally in <span class="hlt">freely</span>-moving animals. We describe here external high-resolution real-time fluorescent optical imaging of metastatic tumors in live mice. Stable high-level green flourescent protein (GFP)-expressing human and rodent cell lines enable tumors and metastasis is formed from them to be externally imaged from <span class="hlt">freely</span>-moving mice. Real-time tumor and metastatic growth were quantitated from whole-body real-time imaging in GFP-expressing melanoma and colon carcinoma models. This GFP optical imaging system is highly appropriate for high throughput in vivo drug screening.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26031070','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26031070"><span>[Spatial-temporal distributions of <span class="hlt">dissolved</span> inorganic carbon and its affecting factors in the Yellow River estuary].</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Guo, Xing-Sen; Lü, Ying-Chun; Sun, Zhi-Gao; Wang, Chuan-Yuan; Zhao, Quan-Sheng</p> <p>2015-02-01</p> <p>Estuary is an important area contributing to the global carbon cycle. In order to analyze the spatial-temporal distribution characteristics of the <span class="hlt">dissolved</span> inorganic carbon (DIC) in the surface water of Yellow River estuary. Samples were collected in spring, summer, fall, winter of 2013, and discussed the correlation between the content of DIC and environmental factors. The results show that, the DIC <span class="hlt">concentration</span> of the surface water in Yellow River estuary is in a range of 26.34-39.43 mg x L(-1), and the DIC <span class="hlt">concentration</span> in freshwater side is higher than that in the sea side. In some areas where the salinity is less than 15 per thousand, the DIC <span class="hlt">concentration</span> appears significant losses-the maximum loss is 20.46%. Seasonal distribution of performance in descending order is spring, fall, winter, summer. Through principal component analysis, it shows that water temperature, suspended solids, salinity and chlorophyll a are the main factors affecting the variation of the DIC <span class="hlt">concentration</span> in surface water, their contribution rate is as high as 83% , and alkalinity, pH, <span class="hlt">dissolved</span> organic carbon, <span class="hlt">dissolved</span> oxygen and other factors can not be ignored. The loss of DIC in the low area is due to the calcium carbonate sedimentation. DIC presents a gradually increasing trend, which is mainly due to the effects of water retention time, temperature, outside input and environmental conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24918966','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24918966"><span>Significance of population centers as sources of gaseous and <span class="hlt">dissolved</span> PAHs in the lower Great Lakes.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>McDonough, Carrie A; Khairy, Mohammed A; Muir, Derek C G; Lohmann, Rainer</p> <p>2014-07-15</p> <p>Polyethylene passive samplers (PEs) were used to measure <span class="hlt">concentrations</span> of gaseous and <span class="hlt">dissolved</span> polycyclic aromatic hydrocarbons (PAHs) in the air and water throughout the lower Great Lakes during summer and fall of 2011. Atmospheric Σ15PAH <span class="hlt">concentrations</span> ranged from 2.1 ng/m3 in Cape Vincent (NY) to 76.4 ng/m3 in downtown Cleveland (OH). Aqueous Σ18PAH <span class="hlt">concentrations</span> ranged from 2.4 ng/L at an offshore Lake Erie site to 30.4 ng/L in Sheffield Lake (OH). Gaseous PAH <span class="hlt">concentrations</span> correlated strongly with population within 3-40 km of the sampling site depending on the compound considered, suggesting that urban centers are a primary source of gaseous PAHs (except retene) in the lower Great Lakes region. The significance of distant population (within 20 km) versus local population (within 3 km) increased with subcooled liquid vapor pressure. Most <span class="hlt">dissolved</span> aqueous PAHs did not correlate significantly with population, nor were they consistently related to river discharge, wastewater effluents, or precipitation. Air-water exchange calculations implied that diffusive exchange was a source of phenanthrene to surface waters, while acenaphthylene volatilized out of the lakes. Comparison of air-water fluxes with temperature suggested that the significance of urban centers as sources of <span class="hlt">dissolved</span> PAHs via diffusive exchange may decrease in warmer months.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017APS..DFDA10008A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017APS..DFDA10008A"><span>Prey capture by <span class="hlt">freely</span> swimming flagellates</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Andersen, Anders; Dolger, Julia; Nielsen, Lasse Tor; Kiorboe, Thomas</p> <p>2017-11-01</p> <p>Flagellates are unicellular microswimmers that propel themselves using one or several beating flagella. Here, we explore the dependence of swimming kinematics and prey clearance rate on flagellar arrangement and determine optimal flagellar arrangements and essential trade-offs. To describe near-cell flows around <span class="hlt">freely</span> swimming flagellates we consider a model in which the cell is represented by a no-slip sphere and each flagellum by a point force. For uniflagellates pulled by a single flagellum the model suggests that a long flagellum favors fast swimming, whereas high clearance rate is favored by a very short flagellum. For biflagellates with both a longitudinal and a transversal flagellum we explore the helical swimming kinematics and the prey capture sites. We compare our predictions with observations of swimming kinematics, prey capture, and flows around common marine flagellates. The Centre for Ocean Life is a VKR Centre of Excellence supported by the Villum Foundation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28825703','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28825703"><span>Virtual reality for <span class="hlt">freely</span> moving animals.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stowers, John R; Hofbauer, Maximilian; Bastien, Renaud; Griessner, Johannes; Higgins, Peter; Farooqui, Sarfarazhussain; Fischer, Ruth M; Nowikovsky, Karin; Haubensak, Wulf; Couzin, Iain D; Tessmar-Raible, Kristin; Straw, Andrew D</p> <p>2017-10-01</p> <p>Standard animal behavior paradigms incompletely mimic nature and thus limit our understanding of behavior and brain function. Virtual reality (VR) can help, but it poses challenges. Typical VR systems require movement restrictions but disrupt sensorimotor experience, causing neuronal and behavioral alterations. We report the development of FreemoVR, a VR system for <span class="hlt">freely</span> moving animals. We validate immersive VR for mice, flies, and zebrafish. FreemoVR allows instant, disruption-free environmental reconfigurations and interactions between real organisms and computer-controlled agents. Using the FreemoVR platform, we established a height-aversion assay in mice and studied visuomotor effects in Drosophila and zebrafish. Furthermore, by photorealistically mimicking zebrafish we discovered that effective social influence depends on a prospective leader balancing its internally preferred directional choice with social interaction. FreemoVR technology facilitates detailed investigations into neural function and behavior through the precise manipulation of sensorimotor feedback loops in unrestrained animals.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1998APS..MAR.X3208B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1998APS..MAR.X3208B"><span><span class="hlt">Freely</span> Suspended Two-Dimensional Electron Gases.</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Blick, Robert; Monzon, Franklin; Roukes, Michael; Wegscheider, Werner; Stern, Frank</p> <p>1998-03-01</p> <p>We present a new technique that has allowed us to build the first <span class="hlt">freely</span> suspended two-dimensional electron gas devices from AlGaAs/GaAs/AlAs heterostructures. This technique is based upon specially MBE grown structures that include a sacrificial layer. In order to design the MBE layer sequence, the conduction band lineup for these samples was modelled numerically. The overall focus of this work is to provide a new approach for studies of the quantum mechanical properties of nanomachined structures. Our current experiments are directed toward use of these techniques for research on very high frequency nanomechanical resonators. The high mobility 2DEG system provides a unique approach to realizing wideband, extremely sensitive displacement detection, using the piezoelectric properties of GaAs to modulate a suspended nanometer-scale HEMT. This approach offers promise for sensitive displacement detectors with sub-nanometer resolution and bandwidths into the microwave range.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4497649','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4497649"><span><span class="hlt">Dissolved</span> Gases and Ice Fracturing During the Freezing of a Multicellular Organism: Lessons from Tardigrades</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Kletetschka, Gunther; Hruba, Jolana</p> <p>2015-01-01</p> <p>Abstract Three issues are critical for successful cryopreservation of multicellular material: gases <span class="hlt">dissolved</span> in liquid, thermal conductivity of the tissue, and localization of microstructures. Here we show that heat distribution is controlled by the gas amount <span class="hlt">dissolved</span> in liquids and that when changing the liquid into solid, the <span class="hlt">dissolved</span> gases either form bubbles due to the absence of space in the lattice of solids and/or are migrated toward the <span class="hlt">concentrated</span> salt and sugar solution at the cost of amount of heat required to be removed to complete a solid-state transition. These factors affect the heat distribution in the organs to be cryopreserved. We show that the gas <span class="hlt">concentration</span> issue controls fracturing of ice when freezing. There are volumetric changes not only when changing the liquid into solid (volume increases) but also reduction of the volume when reaching lower temperatures (volume decreases). We discuss these issues parallel with observations of the cryosurvivability of multicellular organisms, tardigrades, and discuss their analogy for cryopreservation of large organs. PMID:26309797</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=64980&keyword=space+AND+force&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=64980&keyword=space+AND+force&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>THE BUBBLE STRIPPING METHOD FOR DETERMINING <span class="hlt">DISSOLVED</span> HYDROGEN (H2) IN WELL WATER</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>The Bubble Strip Method was developed for determining <span class="hlt">concentrations</span> of <span class="hlt">dissolved</span> H2 in ground water (1). This information canaid in assessing the viability of employing the strategyof monitored natural attenuation (MNA) to restore sites contaminated with chlorinated hydrocarbon...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.fs.usda.gov/treesearch/pubs/33144','TREESEARCH'); return false;" href="https://www.fs.usda.gov/treesearch/pubs/33144"><span>Fluorescence characteristics and biodegradability of <span class="hlt">dissolved</span> organic matter in forest and wetland soils from coastal temperate watersheds in southeast Alaska</span></a></p> <p><a target="_blank" href="http://www.fs.usda.gov/treesearch/">Treesearch</a></p> <p>Jason B. Fellman; David V. D' Amore; Eran Hood; Richard D. Boone</p> <p>2008-01-01</p> <p>Understanding how the <span class="hlt">concentration</span> and chemical quality of <span class="hlt">dissolved</span> organic matter (DOM) varies in soils is critical because DOM influences an array of biological, chemical, and physical processes. We used PARAFAC modeling of excitation-emission fluorescence spectroscopy, specific UV absorbance (SUVA254) and biodegradable <span class="hlt">dissolved</span> organic...</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_25 --> <div class="footer-extlink text-muted" style="margin-bottom:1rem; text-align:center;">Some links on this page may take you to non-federal websites. 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