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Sample records for dissolved metal concentration

  1. Comparison of dissolved and total metals concentrations from acute tests with saltwater organisms

    SciTech Connect

    Lussier, S.M.; Boothman, W.S.; Champlin, D.; Poucher, S.; Helmstetten, A.

    1999-05-01

    Aquatic life criteria (ALC) have traditionally been expressed for meals in terms of total-recoverable or acid-soluble concentrations. Recent US Environmental protection Agency policy recommended use of dissolved metal concentrations for setting water quality standards. Criteria derived from previous tests could be expressed in terms of dissolved metals if ratios of dissolved-to-total concentrations in those tests were consistent. Using those metals with insufficient dissolved metals data to directly derive criteria (arsenic (III), cadmium, chromium (VI), lead, nickel, selenium (IV), and zinc), the authors measured both total and dissolved metal concentrations in acute saltwater static and flow-through tests. Exposure conditions simulated those of original tests used to derive ALC. Partitioning of metals between dissolved and particulate forms was very consistent. Dissolved metal concentrations were greater than 90% of total concentrations in all tests, exceeding 95% in 10 of 13 tests. Dissolved-to-total metal ratios did not vary significantly with concentration, time, or type of test. Biological responses were consistent with historical data. Results implied that in acute saltwater toxicity tests used to establish ALC, metals were primarily dissolved. Thus criteria developed for metals based on total concentrations should be equally valid when expressed in terms of dissolved concentrations.

  2. Dissolved:total metals concentrations in marine acute toxicity test simulations

    SciTech Connect

    Lussier, S.M.; Boothman, W.S.; Champlin, D.; Poucher, S.; Helmstetter, A.

    1995-12-31

    Use of water quality criteria expressed as dissolved metal is recommended by the US EPA, Office of Water, because ``dissolved metal more closely approximates the bioavailable fraction of metal in the water column than does total recoverable metal.`` Water quality criteria (WQC) are expressed in terms of total recoverable or acid-soluble metals concentrations; in part because few toxicity tests with aquatic organisms include measurement of dissolved metals. Therefore, if WQC are to be expressed as dissolved, complete retesting or derivation of dissolved:total (D:T) metals relationships to adjust existing criteria were required. To derive D:T ratios, simulated tests were conducted using concentrations and species similar to those used to derive original criteria. Dissolved (<0.45/{micro}) and total recoverable metals were measured to determine the partitioning relationship under these experimental conditions and convert criteria to reflect dissolved metals concentrations. Simulations were conducted with arsenic (III), cadmium, chromium (VI), lead, nickel, selenium, and zinc. In all simulations, average dissolved metals comprised 93--100% of total metals measured. Dissolved:total ratios did not significantly differ for a given metal throughout each test among test type or treatment concentration. Biological results, while insufficient to derive criteria directly, were generally consistent with results of historical biological response data. These results demonstrate that, under the conditions employed, i.e, short exposure periods (2--4 days) and low particulate load typical of these tests, metals are essentially not removed from solution onto particles. This does not imply that such partitioning is representative of conditions in natural waters, but rather that in the historical acute toxicity tests used to establish water quality criteria, metals were primarily dissolved.

  3. [Concentrations and Speciation of Dissolved Heavy Metal in Rainwater in Guiyang, China].

    PubMed

    Zhu, Zhao-zhou; Li, Jun; Wang, Zhi-ru

    2015-06-01

    In order to understand the pollution situation, as well as seasonal changes in characteristics and speciation of dissolved heavy metals in acid rain control zone, the concentrations of dissolved heavy metals in rainwater collected at Guiyang were measured using inductively coupled plasma mass spectrometry (ICP-MS). And the speciation of dissolved heavy metals was further simulated by PHREEQC model. The results showed that the dissolved Co, Ni, Cu, Zn and Cd concentrations were low and not higher than the national standards for drinking water quality in China. The dissolved Pd concentrations were high in fall and winter and higher than the national standards for drinking water quality in China. The Co and Ni in rainwater mainly came from the crust and there was almost no human impact. The Cu, Zn, Cd and Pd pollutions in rainwater were affected by human activity with different levels. The degrees of contamination in autumn and winter were more serious than those in spring and summer. The free metal ion species was the dominant form of dissolved heavy metal, accounting for 47.27%-95.28% of the dissolved metal in rainwater from Guiyang city. The free metal ion species was followed in abundance by Metal-Oxalate and Metal-sulfate complexes that accounted for 0.72% -51.87% and 0.50%-7.66%, respectively. The acidity of rainwater, acid type as well as content of ligand more likely controlled the distribution of dissolved heavy metal in precipitation. PMID:26387294

  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.B.

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

    NASA Astrophysics Data System (ADS)

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

    2003-09-01

    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.

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

    USGS Publications Warehouse

    Nimick, D.A.; Gammons, C.H.; Cleasby, T.E.; Madison, J.P.; Skaar, D.; Brick, C.M.

    2003-01-01

    Substantial diel (24-hour) cycles in dissolved (0.1-??m 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. 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 h) 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 was 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. Site specific water compositions, including time-integrated dissolved metal concentrations determined from DGT, a competitive, multiple-toxicant biotic ligand model, and the Windemere Humic Aqueous Model Version 6.0 (WHAM VI) were used to determine the equilibrium 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.

  8. Trace metal concentrations in post-hatching cuttlefish Sepia officinalis and consequences of dissolved zinc exposure.

    PubMed

    Le Pabic, Charles; Caplat, Christelle; Lehodey, Jean-Paul; Milinkovitch, Thomas; Koueta, Noussithé; Cosson, Richard Philippe; Bustamante, Paco

    2015-02-01

    In this study, we investigated the changes of 13 trace metal and metalloid concentrations (i.e. Ag, As, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb, Se, V, Zn) and their subcellular fractionation in juvenile cuttlefish Sepia officinalis reared in controlled conditions between hatching and 2 months post-hatching. In parallel, metallothionein concentrations were determined. Our results highlighted contrasting changes of studied metals. Indeed, As and Fe concentrations measured in hatchlings suggested a maternal transfer of these elements in cuttlefish. The non-essential elements Ag and Cd presented the highest accumulation during our study, correlated with the digestive gland maturation. During the 6 first weeks of study, soluble fractions of most of essential trace metals (i.e. Co, Cr, Cu, Fe, Se, Zn) slowly increased consistently with the progressive needs of cuttlefish metabolism during this period. In order to determine for the first time in a cephalopod how metal concentrations and their subcellular distributions are impacted when the animals are trace metal-exposed, we studied previously described parameters in juveniles exposed to dissolved Zn at environmental (i.e. 50 μg l(-1)) and sublethal (i.e. 200 μg l(-1)) levels. Moreover, oxidative stress (i.e. glutathione S-transferase (GST), superoxide dismutase (SOD) and catalase activities, and lipid peroxidation (LPO)) was assessed in digestive gland and gills after 1 and 2 months exposures. Our results highlighted no or low ability of this stage of life to regulate dissolved Zn accumulation during the studied period, consistently with high sensitivity of this organism. Notably, Zn exposures caused a concentration-dependent Mn depletion in juvenile cuttlefish, and an increase of soluble fraction of Ag, Cd, Cu without accumulation modifications, suggesting substitution of these elements (i.e. Mn, Ag, Cd, Cu) by Zn. In parallel, metallothionein concentrations decreased in individuals most exposed to Zn. Finally, no

  9. METHOD OF DISSOLVING URANIUM METAL

    DOEpatents

    Slotin, L.A.

    1958-02-18

    This patent relates to an economicai means of dissolving metallic uranium. It has been found that the addition of a small amount of perchloric acid to the concentrated nitric acid in which the uranium is being dissolved 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.

  10. Dissolved, particulate and acid-leachable trace metal concentrations in North Atlantic precipitation collected on the Global Change Expedition

    SciTech Connect

    Lim, B.; Jickells, T.D. )

    1990-12-01

    Atmospheric inputs of trace metals into surface waters are an important pathway for the oceanic biogeochemical cycling of many trace constituents. Rainwater samples from six precipitation events were collected on board ship during legs 3 and 4 of the Global Change Expedition over the North Atlantic Ocean and analyzed for dissolved, particulate (Al and Pb), and acid-leachable trace metals (Al, Fe, Mn, Cd, Cu, Pb, Zn). Acid-leachable concentrations of the elements were similar to reported values from the North Atlantic and Pacific Oceans which were measured using comparable acidification procedures. Concentrations of dissolved and particulate Al and Pb were determined in rain events acid-leachable and total trace metal concentrations suggest that the acid-leachable fraction of metals can significantly underestimate total concentrations of crustal elements in rain. The solubilities of Al and Pb in precipitation were variable and mean solubilities of the elements were 13% and 45%, respectively. Recycled sea salt components were less than 14% for Al, Fe, Mn, Pb, Cd, Cu, and Zn, indicating that the net trace metal flux is from the atmosphere to the oceans. Deep sea particle fluxes for these metals through the western tropical North Atlantic exceed atmospheric deposition fluxes by a factor of 18 to 41. 57 refs., 2 figs., 12 tabs.

  11. METHOD OF DISSOLVING METALLIC URANIUM

    DOEpatents

    Schulz, W.W.

    1959-07-28

    A process is presented for more rapidly dissolving metallic uranium which comprises contacting the uranium with a mixture of nitric and phosphoric acids. The preferred concentration is a mixture which is about 10 M in nitric acid and between 0.1 to 0.15 M in phosphoric acid.

  12. Dissolved Concentrations, Sources, and Risk Evaluation of Selected Metals in Surface Water from Mangla Lake, Pakistan

    PubMed Central

    Saleem, Muhammad; Iqbal, Javed; Shah, Munir H.

    2014-01-01

    The present study is carried out for the assessment of water quality parameters and selected metals levels in surface water from Mangla Lake, Pakistan. The metal levels (Ca, Cd, Co, Cr, Cu, Fe, K, Li, Mg, Mn, Na, Ni, Pb, Sr, and Zn) were determined by flame atomic absorption spectrophotometry. Average levels of Cd, Co, Cr, Ni, and Pb were higher than the allowable concentrations set by national and international agencies. Principal component analysis indicated significant anthropogenic contributions of Cd, Co, Cr, Ni, and Pb in the water reservoir. Noncarcinogenic risk assessment was then evaluated using Hazard Quotient (HQing/derm) and Hazard Index (HIing/derm) following USEPA methodology. For adults and children, Cd, Co, Cr, and Pb (HQing > 1) emerged as the most important pollutants leading to noncarcinogenic concerns via ingestion route, whereas there was no risk via dermal contact of surface water. This study helps in establishing pollutant loading reduction goal and the total maximum daily loads, and consequently contributes to preserve public health and develop water conservation strategy. PMID:24744690

  13. 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., II; 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

  14. 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.

  15. 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.

  16. Influence of in-stream diel concentration cycles of dissolved trace metals on acute toxicity to one-year-old cutthroat trout (Oncorhynchus clarki lewisi)

    USGS Publications Warehouse

    Nimick, D.A.; Harper, D.D.; Farag, A.M.; Cleasby, T.E.; MacConnell, E.; Skaar, D.

    2007-01-01

    Extrapolating results of laboratory bioassays to streams is difficult, because conditions such as temperature and dissolved metal concentrations 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 dissolved (0.1-??m filtration) metal concentrations that either exhibited the diel variation observed in streams or were controlled at a constant value. Cadmium and Zn concentrations 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 concentration cycle. In High Ore Creek (40 km south of Helena, MT, USA), survival (33%) after exposure to natural diel-fluctuating Zn concentrations (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 concentration (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 concentrations (range, 266-522 ??g/L; mean, 399 ??g/L) was significantly (p = 0.022) higher than survival (50%) in the constant-concentration treatment (392 ??g/L). Survival likely was greater in these diel treatments, both because the periods of lower metal concentrations provided some relief for the fish and because toxicity during periods of higher metal concentrations 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 concentration cycles of Zn (and, perhaps, Cd) for the hydrologie conditions tested. ?? 2007 SETAC.

  17. Cellular partitioning of nanoparticulate versus dissolved metals in marine phytoplankton.

    PubMed

    Bielmyer-Fraser, Gretchen K; Jarvis, Tayler A; Lenihan, Hunter S; Miller, Robert J

    2014-11-18

    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 dissolved 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 dissolved 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 dissolved 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 dissolved 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. Concentration-dependent metal accumulation and reduced population growth were observed in T. weissflogii exposed to nanometal oxides, as well as dissolved metals. Significant effects on population growth were observed at the lowest concentrations tested for all metals, with similar toxicity for both dissolved and nanoparticulate metals. Cellular metal distribution, however, markedly differed between T. weissflogii exposed to nanometal oxides versus those exposed to dissolved metals. Metal concentrations were highest in the algal cell wall when cells were exposed to metal oxide nanoparticles, whereas algae exposed to dissolved 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

  18. TOTAL DISSOLVED AND BIOAVAILABLE METALS AT LAKE TEXOMA MARINAS

    EPA Science Inventory

    Dissolved 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 concentrations in marina water were Na and Ca, followed by Mg an...

  19. Summary of Dissolved Concentration Limits

    SciTech Connect

    Yueting Chen

    2001-06-11

    According to the Technical Work Plan titled Technical Work Plan for Waste Form Degradation Process Model Report for SR (CRWMS M&O 2000a), the purpose of this study is to perform abstractions on solubility limits of radioactive elements based on the process-level information and thermodynamic databases provided by Natural Environment Program Operations (NEPO) and Waste Package Operations (WPO). The scope of this analysis is to produce solubility limits as functions, distributions, or constants for all transported radioactive elements identified by the Performance Assessment Operations (PAO) radioisotope screening. Results from an expert elicitation for solubility limits of most radioactive elements were used in the previous Total System Performance Assessments (TSPAs). However, the elicitation conducted in 1993 does not meet the criteria set forth by the U.S. Nuclear Regulatory Commission (NRC) due to lack of documentation and traceability (Kotra et al. 1996, Section 3). Therefore, at the Waste Form Abstraction Workshop held on February 2-4, 1999, at Albuquerque, New Mexico, the Yucca Mountain Site Characterization Project (YMP) decided to develop geochemical models to study solubility for the proposed Monitored Geologic Repository. WPO/NEPO is to develop process-level solubility models, including review and compilation of relevant thermodynamic data. PAO's responsibility is to perform abstractions based on the process models and chemical conditions and to produce solubility distributions or response surfaces applicable to the proposed repository. The results of this analysis and conceptual model will feed the performance assessment for Total System Performance Assessment--Site Recommendation (TSPA-SR) and Total System Performance Assessment--License Application (TSPA-LA), and to the Waste Form Degradation Process Model Report section on concentration limits.

  20. Removal of dissolved metals by plant tissue

    SciTech Connect

    Scott, C.D. )

    1992-04-25

    Various types of microbial biomass have been shown to adsorb metals dissolved in aqueous media. It has now been demonstrated that certain plant tissues are also effective for this type of adsorption process. In particular, tomato and tobacco roots harvested from field-grown plants were shown to adsorb Sr from an aqueous solution of SrCl[sub 2]. Distribution coefficients in excess of 550 were measured and the adsorption isotherms at 25 C could be fitted to Langmuir-type expressions. The bioadsorbent could be regenerated and metals recovered by either a reduction in the pH to less than 2.0 or by use of a concentrated chloride salt solution.

  1. Dissolved Trace metal distributions and speciation in Yellow Sea, China

    NASA Astrophysics Data System (ADS)

    Li, Li; Wang, Xiaojing; Zhang, Cuiqin; Liu, Jihua; Shi, Xuefa

    2016-04-01

    Trace metals play an important role in marine biogeochemical cycling processes. However, owing to the lack of trace-metal clean sampling and analytical techniques, high quality data for dissolved trace metals in coastal seawaters of China are scarce. In this study, by employing stringent trace-metal clean sampling and analytical techniques, we investigated spatial distribution patterns of several dissolved trace metals (Cu, Ni, Co, Pb, Cd, Zn, and Ag) in Yellow Sea and Bohai Sea of China, and discussed their potential sources and sinks. In general, the dissolved metal concentrations decreased from Bohai Sea to Yellow Sea, and from nearshore to offshore. Despite the severe contamination status reported in coastal seawaters of China, the trace metal concentrations found in seawater are comparable to the concentrations found in pristine coastal seawaters of the US and the EU. In the meantime, the speciation of several metals (Cu, Pb, Zn, Cd) were also studied with the electrochemical (ASV and CLE-CSV) methods in the Yellow Sea. Natural organic ligands were found in seawaters that strongly complexed with dissolved metals. The concentrations and binding constants of the complexing ligands for each metal were reported and compared with the ones found in other coastal seawaters.

  2. 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.

    2015-01-01

    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.

  3. Fluctuation of dissolved heavy metal concentrations in the leachate from anaerobic digestion of municipal solid waste in commercial scale landfill bioreactors: The effect of pH and associated mechanisms.

    PubMed

    Xie, S; Ma, Y; Strong, P J; Clarke, W P

    2015-12-15

    Heavy metals present in landfill leachate have infrequently been related to complete anaerobic degradation municipal solid waste (MSW) due to discrete ages of deposited MSW layers and leachate channelling in landfills. In this study, anaerobic digestion of MSW was performed in two enclosed 1000 tonne bioreactors using a unique flood and drain process. Leachates were characterised in terms of pH, soluble chemical oxygen demand, volatile fatty acids (VFAs), ammonium nitrogen and heavy metals over the entire course of digestion. All parameters, including pH, fluctuated during acidogenesis, acetogenesis and methanogenesis, which strongly impacted on the dynamics of dissolved heavy metal concentrations. The simulation of dissolution and precipitation processes indicated that metal sulphide precipitation was not a factor as metal concentrations exceeded solubility limits. The correlation of pH and dissolved heavy metal concentrations indicated that other, mechanisms were involved in the homogenised conditions within the bioreactors. Beside dissolution and precipitation, the main processes most likely involved in metal distributions were adsorption (Zn, Cu, Ni, Pb and Cd), complexation (Cr) or combinations of both process (As and Co). PMID:26259097

  4. DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS

    SciTech Connect

    NA

    2004-11-22

    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 modeling activity is to predict dissolved concentrations or solubility limits for 14 elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) important to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are in the form of tabulated functions with pH and log (line integral) CO{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. The output data from this report are fundamental inputs for Total System Performance Assessment for the License Application (TSPA-LA) 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 all of the actinides. These models cover broad ranges of environmental conditions so that they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified or otherwise addressed.

  5. Dissolved Concentration Limits of Radioactive Elements

    SciTech Connect

    Y. Chen; E.R. Thomas; F.J. Pearson; P.L. Cloke; T.L. Steinborn; P.V. Brady

    2003-06-20

    The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of radioactive elements under possible repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, and measurements made in laboratory experiments and field work. The scope of this modeling activity is to predict dissolved concentrations or solubility limits for 14 radioactive elements (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium), which are important to calculated dose. Model outputs are mainly in the form of look-up tables plus one or more uncertainty terms. The rest are either in the form of distributions or single values. The results of this analysis are fundamental inputs for total system performance assessment to constrain the release of these elements from waste packages and the engineered barrier system. Solubilities of plutonium, neptunium, uranium, americium, actinium, thorium, protactinium, lead, and radium have been re-evaluated using the newly updated thermodynamic database (Data0.ymp.R2). For all of the actinides, identical modeling approaches and consistent environmental conditions were used to develop solubility models in this revision. These models cover broad ranges of environmental conditions so that they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, activity coefficients, and selection of solubility controlling phase have been quantified or otherwise addressed. Moreover, a new blended plutonium solubility model has been developed in this revision, which gives a mean solubility that is three orders of magnitude lower than the plutonium solubility model used for the Total System Performance Assessment for the Site Recommendation. Two alternative neptunium solubility models have also been

  6. DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS

    SciTech Connect

    P. Bernot

    2005-07-13

    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 and 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 or

  7. 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.

  8. The seasonal influence on the spatial distribution of dissolved selected metals in Lake Naivasha, Kenya

    NASA Astrophysics Data System (ADS)

    Kamau, Joseph Nyingi; Gachanja, Anthony; Ngila, Catherine; Kazungu, Johnson Michael; Zhai, Mingzhe

    Lake Naivasha is the only freshwater Lake in Rift Valley, in Kenya. It lies in a fertile semi-arid basin. The Lake has no surface water outlet and is presumed to be under stress. Dissolved metals are directly taken up by bacteria, algae, plants, and planktonic and benthic organisms. Dissolved metals can also adsorb to particulate matter in water column and enter aquatic organisms through various routes. Cadmium, copper, lead and zinc may bioaccumulate within lower organisms, yet they do not biomagnify up the food chain as do mercury and selenium. This study reports on the levels and distribution of dissolved heavy metals and investigates the influence of physicochemical parameters on metal mobilization. The bioavailability of selected metals was investigated by relating the levels of dissolved metals to that in fish. Water abstraction for irrigation and domestic use, compounded with organic matter inflow will affect physicochemical parameters and hence influences the mobilization of heavy metals. Dissolved Zn correlated highly with sediment pH (r = 0.67) indicating that dissolution increases with increase in pH. In addition, the fact that the pH also correlated positively with organic matter r = 0.50, Eh r = 0.63, temperature r = 0.56 and dissolved oxygen r = 56, would suggest that organic bound Zn contributed significantly to the concentration of dissolved Zn. In situ flux experiments indicated that the fringing papyrus reeds located along the shores of Lake Naivasha provided sites for metal immobilization due to their coprecipitation on redox sensitive.

  9. 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.

  10. Dissolved oxygen concentration affects hybrid striped bass growth

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Management of dissolved oxygen (DO) concentration in ponds at night during the growing season is important because fish growth and yield are greater in ponds with higher nightly DO concentrations. Three studies were conducted to quantify performance traits and metabolic responses of hybrid striped b...

  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. CONTINUOUS DISSOLVER EXTRACTOR FOR PROCESSING METAL

    DOEpatents

    Lemon, R.B.; Buckham, J.A.

    1959-02-01

    An apparatus is presented for the continuous dissolution of metal slugs in an aqueous acid and sequential continuous extraction of selected metal values from the acid solution by counter-current contact with an organic solvent. The apparatus comprises a cylindrical tank divided into upper and lower sections. Dissolution of the metal slug takes place in the lower section and the solution so produced is continuously fed to the topmost plate of the upper extraction section. An immiscible organic extractant is continuously passed by a pulsing pump into the lowermost unit of the extraction section. Suitable piping and valving permits of removing the aqueous raffinate solution from the lowermost portion of the extraction section, and simultaneous removal of organic solvent extractant containing the desired product from the uppermost portion of the extraction section.

  13. Metallization problems with concentrator cells

    NASA Technical Reports Server (NTRS)

    Iles, P. A.

    1983-01-01

    Cells used with concentrators have similar contact requirements to other cells, but operation at high intensity imposes more than the usual demands on the metallization. Overall contact requirements are listed and concentrator cell requirements are discussed.

  14. Variations in dissolved organic carbon concentrations across peatland hillslopes

    NASA Astrophysics Data System (ADS)

    Boothroyd, I. M.; Worrall, F.; Allott, T. E. H.

    2015-11-01

    Peatlands are important terrestrial carbon stores and dissolved organic carbon (DOC) is one of the most important contributors to carbon budgets in peatland systems. Many studies have investigated factors affecting DOC concentration in peatland systems, yet hillslope position has been thus far overlooked as a variable that could influence DOC cycling. This study investigates the importance of hillslope position with regard to DOC cycling. Two upland peat hillslopes were studied in the Peak District, UK, to determine what impact, if any, hillslope position had upon DOC concentration. Hillslope position was found to be a significant factor affecting variation in soil pore water DOC concentration, with bottom-slope positions having significantly lower DOC concentrations than up-slope because of dilution of DOC as water moves down-slope and is flushed out of the system via lateral throughflow. Water table drawdown on steeper mid-slopes increased DOC concentrations through increased DOC production and extended residence times allowing a build-up of humic-rich DOC compounds. Hillslope position did not significantly affect DOC concentrations in surface runoff water because of the dilution of near-surface soil pore water by precipitation inputs, while stream water had similar water chemistry properties to soil pore water under low-flow conditions.

  15. Dissolved and particulate metals dynamics in a human impacted estuary from the SW Atlantic

    NASA Astrophysics Data System (ADS)

    La Colla, Noelia S.; Negrin, Vanesa L.; Marcovecchio, Jorge E.; Botté, Sandra E.

    2015-12-01

    In order to evaluate metal behavior in urban stressed estuaries, the distribution of major elements (Fe and Mn) and trace elements (Cd and Cu) between suspended particulate matter (SPM) and subsuperficial seawater in the Bahía Blanca Estuary, Argentina, was studied. Four different impacted areas were selected to study the spatial and temporal distribution of these metals in an estuary in continuous industrial development and where an environmental law was implemented to supervise industrial discharges in waters. Sampling was performed within intertidal areas. Physicochemical conditions usually influence the partitioning of metals between the dissolved and particulate fraction thus, salinity, pH, turbidity, temperature and dissolved oxygen were also measured. Dissolved metals were analyzed with atomic absorption spectrophotometry (AAS) and the particulate fraction with inductively coupled plasma optical emission spectrometry (ICP OES). Metals concentration ranges, within the dissolved fraction (μg/L), were from below the method detection limit for all the elements to 4.7 in the case of Cd, 6.0 for Cu and 62 for Fe. Minimum and maximum values in the particulate fraction (μg/g, d.w.) were from below the method detection limit to 11 for Cd; from 24 to 220 for Cu and from 630 to 1500 for Mn. For Fe, concentrations ranged from 2.2 to 9.6 (%). The general order of the dissolved/particulate partition coefficients (Log10Kds) for the studied metals, considering mean values, were: Fe (7.0) > Cu (4.2) > Cd (3.3). The metals values as well as the physicochemical parameters showed temporal variations and many correlations were found among them. Log10Kd Fe values were the highest, highlighting its strong affinity for particles. Metals concentrations were sometimes higher than those from other polluted areas as well as from previous studies from the same estuary, which highlights the potential impact of these elements in the study area. The concentrations of particulate metals

  16. Corals concentrate dissolved inorganic carbon to facilitate calcification.

    PubMed

    Allison, Nicola; Cohen, Itay; Finch, Adrian A; Erez, Jonathan; Tudhope, Alexander W

    2014-01-01

    The sources of dissolved inorganic carbon (DIC) used to produce scleractinian coral skeletons are not understood. Yet this knowledge is essential for understanding coral biomineralization and assessing the potential impacts of ocean acidification on coral reefs. Here we use skeletal boron geochemistry to reconstruct the DIC chemistry of the fluid used for coral calcification. We show that corals concentrate DIC at the calcification site substantially above seawater values and that bicarbonate contributes a significant amount of the DIC pool used to build the skeleton. Corals actively increase the pH of the calcification fluid, decreasing the proportion of DIC present as CO2 and creating a diffusion gradient favouring the transport of molecular CO2 from the overlying coral tissue into the calcification site. Coupling the increases in calcification fluid pH and [DIC] yields high calcification fluid [CO3(2-)] and induces high aragonite saturation states, favourable to the precipitation of the skeleton. PMID:25531981

  17. When dissolved is not truly dissolved--the importance of colloids in studies of metal sorption on organic matter.

    PubMed

    Schijf, Johan; Zoll, Alison M

    2011-09-01

    In controlled metal sorption experiments, the equilibrium distribution coefficient is a key variable quantifying sorbate partitioning across the solid-solution interface. Separation of metals into 'dissolved' and 'particulate' fractions is commonly achieved with syringe filtration, where the boundary is somewhat arbitrarily dictated by the limited selection of available pore sizes. Investigations involving natural organic matter, such as bacterial cells or plant tissues, are especially prone to experimental artifacts if the substrate releases abundant colloidal compounds that contribute to sorption by binding free metal cations in a pH-dependent fashion yet pass through conventional filters, causing the truly dissolved fraction to be grossly overestimated. We observed this phenomenon during a study of lanthanide sorption on a marine macroalga, Ulva lactuca, as a function of pH. At low ionic strength, distribution coefficients calculated for a 0.22-μm size cutoff falsely imply that metal sorption reverses to gradual release above pH 4.6, instead of continuing to increase. Centrifuging the filtrates in Amicon® Ultra units (30 and 3 kDa molecular weight cutoff) revealed a mounting proportion of colloid-bound metal, constituting up to 95% of the 'dissolved' (<0.22 μm) fraction near pH 8. Measurements of DOC concentrations suggest this being due to pH-dependent binding of free metal cations to a fixed pool of organic colloids. The process is well described with a simple 2-site Langmuir isotherm in 0.05, 0.5, and 5.0M NaCl. Using this model to correct the original distribution coefficients not only removed the spurious reversal at low ionic strength, but also uncovered a prominent suppressive effect on the intermediate and high ionic strength data that had initially gone undetected. Ultra-filtration may thus be an essential analytical tool for proper characterization and interpretation of metal sorption on organic matter over a wide range of experimental conditions

  18. Bead and Process for Removing Dissolved Metal Contaminants

    SciTech Connect

    Summers, Bobby L., Jr.; Bennett, Karen L.; Foster, Scott A.

    2005-01-18

    A bead is provided which comprises or consists essentially of activated carbon immobilized by crosslinked poly (carboxylic acid) binder, sodium silicate binder, or polyamine binder. The bead is effective to remove metal and other ionic contaminants from dilute aqueous solutions. A method of making metal-ion sorbing beads is provided, comprising combining activated carbon, and binder solution (preferably in a pin mixer where it is whipped), forming wet beads, and heating and drying the beads. The binder solution is preferably poly(acrylic acid) and glycerol dissolved in water and the wet beads formed from such binder solution are preferably heated and crosslinked in a convection oven.

  19. Measuring Hydrogen Concentrations in Metals

    NASA Technical Reports Server (NTRS)

    Danford, M. D.

    1985-01-01

    Commercial corrosion-measurement system adapted to electrochemical determination of hydrogen concentrations in metals. New technique based on diffusion of hydrogen through foil specimen of metal. In sample holder, hydrogen produced on one side of foil, either by corrosion reaction or by cathodic current. Hydrogen diffused through foil removed on other side by constant anode potential, which leads to oxidation of hydrogen to water. Anode current is measure of concentration of hydrogen diffusing through foil. System used to study hydrogen uptake, hydrogen elimination by baking, effect of heat treatment, and effect of electroplating on high-strength steels.

  20. Understanding Dissolved and Colloidal Metal Transport and Transformation - Pathways for Aquatic Toxicity

    NASA Astrophysics Data System (ADS)

    Kimball, B. A.; Besser, J. M.

    2004-05-01

    Hundreds of miles of streams in the western United States are affected by the release of metals from weathering of mineralized bedrock and mine wastes. In many cases, historical mining has accelerated these weathering processes and increased concentrations of metals in affected streams. Copper and zinc are two metals that affect aquatic health in such streams. Aquatic toxicity from copper and zinc is thought to be related principally to their dissolved concentrations. But there are alternative pathways that may lead to toxicity. Movement of many metals associated with mine drainage is affected by iron colloidal solids. The initial precipitation of iron hydroxides results in nanometer-sized colloids that subsequently aggregate to form a continuum of particle sizes from about one nanometer to greater than one micrometer. This behavior makes the popular or legal definition of dissolved metals at 0.45 micrometers meaningless in streams affected by mine drainage. Ultrafiltration, using tangential-flow across 10,000-Dalton membranes, provides a means to understand dissolved and colloidal metal concentrations. When ultrafiltration is combined with methods to determine mass loading, it is possible to quantify sources and chemical reactions affecting metals. For example, results from a mass-loading study in Mineral Creek, Colorado, indicate that copper and zinc are contributed to the stream from both mined and unmined sources. As the pH of Mineral Creek changes in response to both neutral and acidic inflows, copper was repeatedly transferred between dissolved and colloidal phases through sorption reactions. When the colloidal phase was dominant, the total load of copper consistently decreased because the colloids are entrained by algae on cobbles and strained by the streambed during hyporheic exchange. Zinc load also decreased during transport, but this was a result of the physical process of water exchange with the hyporheic zone, and not a result of colloidal

  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. PMID:24839192

  2. Atmospheric input of dissolved and particulate metals to the northwestern Mediterranean

    NASA Astrophysics Data System (ADS)

    Guieu, C.; Chester, R.; Nimmo, M.; Martin, J.-M.; Guerzoni, S.; Nicolas, E.; Mateu, J.; Keyse, S.

    Concentrations of trace elements (Al, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) were determined for aerosols, dry deposition, precipitation and total deposition samples collected from five stations on islands and in the coastal zone of the northwestern Mediterranean. Average concentrations of metals are very homogeneous over the sampled area, in particular at the three coastal sites. Cd and Pb are almost entirely of man-made origin, even in Saharan aerosols. For the other metals, the non-crustal fraction is lower in Saharan aerosols than in European aerosols, but there is an important man-made component in the Saharan aerosol, even for metals such as Fe and Cr. This confirms the results of Chester et al. (1992) who concluded that Mediterranean aerosols have a European background upon which are superimposed Saharan inputs. Dry deposition represents an important fraction of the total deposition. Partitioning of total atmospheric deposition between the dissolved and the particulate phases shows that Al, Fe and Cr originating from the atmosphere are mostly in a particulate form in the surface waters. For the other metals studied, the dissolved fraction represents more than 30% of the total input, and for Cd it is almost 100%. Extrapolation shows that more than 50% of the dissolved metals input to the northwestern Mediterranean originates from the atmosphere. Atmospheric input entirely dominates the total external input of pollution-derived elements, such as Pb and Cd. The dissolved input of atmospheric origin is also very important (> 80%) for elements of terrigeneous origin such as A1.

  3. Measurement of Solubility of Metallic Lithium Dissolved in Molten LiCl-Li2O

    NASA Astrophysics Data System (ADS)

    Burak, Adam J.; Simpson, Michael F.

    2016-07-01

    The solubility of lithium metal in molten LiCl-Li2O mixtures has been measured at various concentrations of Li2O ranging from 0 wt.% to 2.7 wt.% at a temperature of approximately 670-680°C. After contacting molten lithium with molten LiCl-Li2O for several hours to achieve equilibrium saturation, samples were taken by freezing the salt onto a room-temperature steel rod and dissolving in water for analysis. Both volume of hydrogen gas generated and volume of titrated HCl were measured to investigate two different approaches to calculating the lithium concentration. There appeared to be no effect of Li2O concentration on the Li solubility in the salt. But the results vary between different methods of deducing the amount of dissolved Li. The H2 collection method is recommended, but care must be taken to ensure all of the H2 has been included.

  4. Dissolved sulfide in groundwater with elevated arsenic concentrations at Winthrop, Maine

    NASA Astrophysics Data System (ADS)

    He, Y.; Zheng, Y.; Zheng, Y.; Locke, D. C.; Simpson, J. H.; Stute, M.

    2001-12-01

    Although sulfur is a biogeochemically significant element because of its strong influence on and response to redox conditions, there are relatively few reliable data sets of trace levels of dissolved sulfide \\(less than1 uM \\) in groundwaters This circumstance results from the relatively high detection limit \\(˜ 1uM \\) of methylene blue colorimetry and the general lack of sensitive methods for field analysis. We were motivated to investigate trace levels of dissolved sulfide because highly insoluble sulfide precipitates of many elements such as As and Fe represent important removal pathways for these metals in reducing groundwaters. Using differential pulse cathodic stripping voltammetry \\(DPCSV\\) capable of detecting 4 nM of dissolved sulfide, we observed that at a site in Winthrop, Maine, groundwater sulfide concentrations ranged from less than 4 nM to ˜ 2000 nM for about a dozen multi-level observation wells under a landfill cap and less than 4 nM to ˜ 7300 nM from several nearby monitoring wells outside the landfill. Sulfide concentrations generally increased when oxygen reduction potential \\(ORP\\) values became more negative. Determination of sulfide should be carried out within 1 hr of sample collection. Samples taken by two methods, \\(1\\) PTFE syringes with luer-lock valves and \\(2\\) BOD bottles show a rapid decline of sulfide following sampling, with up to 90% and 60% losses, respectively, after 24 hrs of storage at 4 ° C. Despite the three orders of magnitude range of dissolved sulfide, arsenic and iron concentrations were all elevated in observational wells installed in a roughly 25 m by 20 m rectangle under the landfill cap, suggesting that As remains mobile under mildly sulfate-reducing conditions. In one well outside of the landfill area, with extremely negative ORP \\(-321 mV\\) and ˜ 7300 nM of dissolved sulfide, groundwater was very low in dissolved As, Fe, and sulfate, suggesting that precipitation of arsenopyrite could be a

  5. METAL-COLLOID PARTITIONING IN ARTIFICIAL INTERSTITIAL WATERS OF MARINE SEDIMENTS: INFLUENCES OF SALINITY, PH AND COLLOIDAL ORGANIC CARBON CONCENTRATION

    EPA Science Inventory

    For decades, heavy metals have been deposited into marine sediments as a result of anthropogenic activities. Depending on their bioavailability, these metals may represent a risk to benthic organisms. Dissolved interstitial water metal concentrations have been shown to be better ...

  6. Historical backcasting of metal concentrations in the Chattahoochee River, Georgia: Population growth and environmental policy

    USGS Publications Warehouse

    Neumann, K.; Lyons, W.B.; Graham, E.Y.; Callender, E.

    2005-01-01

    The impact of increasing urbanization on the quality of a river system has been investigated by examining the current concentration of trace metals in the Chattahoochee River south of Atlanta, GA, and comparing these to previously published historical sediment data from reservoirs along the river. The lack of historical data for dissolved metal concentrations prior to ???1980 requires an approach using these historic metal data from sediment cores. Core data are combined with current suspended load and dissolved metal data to "backcast" dissolved metal concentrations in the metro-Atlanta portion of the Chattahoochee River. The data suggest that the per capita input of dissolved trace metals have actually decreased since the 1920s, but anthropogenic inputs of metal are still a substantial water quality issue. ?? 2005 Elsevier Ltd. All rights reserved.

  7. Metal Ion Speciation and Dissolved Organic Matter Composition in Soil Solutions

    NASA Astrophysics Data System (ADS)

    Benedetti, M. F.; Ren, Z. L.; Bravin, M.; Tella, M.; Dai, J.

    2014-12-01

    Knowledge of the speciation of heavy metals and the role of dissolved organic matter (DOM) in soil solution is a key to understand metal mobility and ecotoxicity. In this study, soil column-Donnan membrane technique (SC-DMT) was used to measure metal speciation of Cd, Cu, Ni, Pb, and Zn in eighteen soil solutions, covering a wide range of metal sources and concentrations. DOM composition in these soil solutions was also determined. Our results show that in soil solution Pb and Cu are dominant in complex form, whereas Cd, Ni and Zn mainly exist as free ions; for the whole range of soil solutions, only 26.2% of DOM is reactive and consists mainly of fulvic acid (FA). The metal speciation measured by SC-DMT was compared to the predicted ones obtained via the NICA-Donnan model using the measured FA concentrations. The free ion concentrations predicted by speciation modelling were in good agreement with the measurements. Diffusive gradients in thin-films gels (DGT) were also performed to quantify the labile metal species in the fluxes from solid phase to solution in fourteen soils. The concentrations of metal species detected by DGT were compared with the free ion concentrations measured by DMT and the maximum concentrations calculated based on the predicted metal speciation in SC-DMT soil solutions. It is concluded that both inorganic species and a fraction of FA bound species account for the amount of labile metals measured by DGT, consistent with the dynamic features of this technique. The comparisons between measurements using analytical techniques and mechanistic model predictions provided mutual validation in their performance. Moreover, we show that to make accurate modelling of metal speciation in soil solutions, the knowledge of DOM composition is the crucial information, especially for Cu; like in previous studies the modelling of Pb speciation is not optimal and an updated of Pb generic binding parameters is required to reduce model prediction uncertainties.

  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. Seasonal variation and sources of dissolved trace metals in Maó Harbour, Minorca Island.

    PubMed

    Martínez-Soto, Marly C; Tovar-Sánchez, Antonio; Sánchez-Quiles, David; Rodellas, Valentí; Garcia-Orellana, Jordi; Basterretxea, Gotzon

    2016-09-15

    The environmental conditions of semi-enclosed coastal water-bodies are directly related to the catchment, human activities, and oceanographic setting in which they are located. As a result of low tidal forcing, and generally weak currents, waters in Mediterranean harbours are poorly renewed, leading to quality deterioration. Here, we characterise the seasonal variation of trace metals (i.e. Co, Cd, Cu, Fe, Mo, Ni, Pb, and Zn) in surface waters, and trace metal content in sediments from Maó Harbour, a semi-enclosed coastal ecosystem in the NW Mediterranean Sea. Our results show that most of the dissolved trace metals in the waters of Maó Harbour exhibit a marked inner-outer concentration gradient, suggesting a permanent input into the inner part of the harbour. In general, metal concentrations in the waters of Maó Harbour are higher than those in offshore waters. Concentration of Cu (21±8nM), Fe (9.2±3.2nM) and Pb (1.3±0.4nM) are particularly high when compared with other coastal areas of the Mediterranean Sea. The concentration of some metals such as Cu and Zn increases during summertime, when the human population and boat traffic increase during the tourism season, and when resuspension from the metal enriched sediments is higher. The evaluation of the metal sources in the harbour reveals that, compared with other putative sources such as runoff, aerosol deposition and fresh groundwater discharges, contaminated sediments are the main source of the metals found in the water column, most likely through vessel-driven resuspension events. This study contributes to the understanding of the processes that control the occurrence and distribution of trace metals in Maó Harbour, thus aiding in the effective management of the harbour, and enhancing the overall quality of the seawater ecosystem. PMID:27163484

  10. AUTOMATIC ANALYSIS OF DISSOLVED METAL POLLUTANTS IN WATER BY ENERGY DISPERSIVE X-RAY SPECTROSCOPY

    EPA Science Inventory

    An automated system for the quantitative determination of dissolved metals such as Fe, Cu, Zn, Ca, Co, Ni, Cr, Hg, Se, and Pb in water is described. The system collects a water sample, preconcentrates the dissolved metals with ion-exchange paper automatically in a sample collecti...

  11. DISSOLVED ORGANIC CARBON (DOC) CONCENTRATIONS IN SMALL STREAMS OF THE GEORGIA PIEDMONT

    EPA Science Inventory

    Dissolved organic matter (DOM) supports microbial activity and contributes to transport of N and P in streams. We have studied the impact of land uses on dissolved organic carbon (DOC) concentrations in 17 Georgia Piedmont headwater streams since January 2001. We classified the w...

  12. Dissolved-solids concentrations of ground water in the Sacramento Valley, California

    USGS Publications Warehouse

    Fogelman, Ronald P.

    1982-01-01

    The general quality of the ground water in the Sacramento Valley , Calif., in terms of dissolved-solids concentration is considered good for irrigation, domestic, and most other uses. This map shows the distribution of dissolved-solids concentrations and is based on about 1,330 chemical analyses collected from about 900 wells between 1974 and 1978. On the west side of the valley some of the smaller streams contribute water of higher dissolved-solids concentrations to the ground water. The sources of these waters are thought to be the upper Cretaceous Chico Formation or marine deposits of Early Cretaceous age that are exposed in the Coast Ranges. (USGS)

  13. Spatio-temporal variability of solid, total dissolved and labile metal: passive vs. discrete sampling evaluation in river metal monitoring.

    PubMed

    Priadi, Cindy; Bourgeault, Adeline; Ayrault, Sophie; Gourlay-Francé, Catherine; Tusseau-Vuillemin, Marie-Hélène; Bonté, Philippe; Mouchel, Jean-Marie

    2011-05-01

    In order to obtain representative dissolved and solid samples from the aquatic environment, a spectrum of sampling methods are available, each one with different advantages and drawbacks. This article evaluates the use of discrete sampling and time-integrated sampling in illustrating medium-term spatial and temporal variation. Discrete concentration index (CI) calculated as the ratio between dissolved and solid metal concentrations in grab samples are compared with time-integrated concentration index (CI) calculated from suspended particulate matter (SPM) collected in sediment traps and labile metals measured by the diffusive gel in thin films (DGT) method, collected once a month during one year at the Seine River, upstream and downstream of the Greater Paris Region. Discrete CI at Bougival was found to be significantly higher than at Triel for Co, Cu, Mn, Ni and Zn, while discrete metal partitioning at Marnay was found to be similar to Bougival and Triel. However, when using time-integrated CI, not only was Bougival CI significantly higher than Triel CI, CI at Marnay was also found to be significantly higher than CI at Triel which was not observed for discrete CI values. Since values are time-averaged, dramatic fluctuations were smoothed out and significant medium-term trends were enhanced. As a result, time-integrated concentration index (CI) was able to better illustrate urbanization impact between sites when compared to discrete CI. The impact of significant seasonal phenomenon such as winter flood, low flow and redox cycles was also, to a certain extent, visible in time-integrated CI values at the upstream site. The use of time-integrated concentration index may be useful for medium- to long-term metal studies in the aquatic environment. PMID:21468423

  14. Stabilization of dissolved trace metals at hydrothermal vent sites: Impact on their marine biogeochemical cycles

    NASA Astrophysics Data System (ADS)

    Sander, Sylvia G.; Powell, Zach D.; Koschinsky, Andrea; Kuzmanovski, Stefan; Kleint, Charlotte

    2014-05-01

    Hydrothermal vents have long been neglected as a significant source of several bioactive trace metals as it was assumed that elements such as Fe, Mn, and Cu etc., precipitate in extensor forming poly-metallic sulfide and oxy-hydroxy sediments in the relative vicinity of the emanation site. However, recently this paradigm has been reviewed since the stabilization of dissolved Fe and Cu from hydrothermal vents was observed [1, 2] and increased concentrations of trace metals can be traced from their hydrothermal source thousands of kilometres through the ocean basins [3]. Furthermore several independent modelling attempts have shown that not only a stabilization of dissolved hydrothermal Fe and Cu is possible [4] but also that hydrothermalism must be a significant source of Fe to be able to balance the Fe-biogeochemical cycle [5]. Here we present new data that gives further evidence of the presence of copper stabilising organic and inorganic compounds in samples characterized by hydrothermal input. We can show that there are systematic differences in copper-complexing ligands at different vent sites such as 5°S on the Mid Atlantic Ridge, Brother Volcano on the Kermadec Arc, and some shallow hydrothermal CO2 seeps in the Bay of Plenty, New Zealand and the Mediterranean Sea. Quantitative and qualitative voltammetric data convincingly indicates that inorganic sulphur and organic thiols form the majority of the strong copper-complexing ligand pool in many of these hydrothermal samples. On average, the high temperature vents had a significantly higher copper binding capacity than the diffuse vents due to higher inorganic sulphur species concentrations. References: [1] Sander, S. G., et al. 2007. Organic complexation of copper in deep-sea hydrothermal vent systems. Environmental Chemistry 4: 81-89 [2] Bennett, S. A., et al. 2008. The distribution and stabilisation of dissolved Fe in deep-sea hydrothermal plumes. Earth and Planetary Science Letters 270: 157-167. [3] Wu J

  15. pH, dissolved oxygen, and adsorption effects on metal removal in anaerobic bioreactors.

    PubMed

    Willow, Mark A; Cohen, Ronald R H

    2003-01-01

    Anaerobic bioreactors were used to test the effect of the pH of influent on the removal efficiency of heavy metals from acid-rock drainage. Two studies used a near-neutral-pH, metal-laden influent to examine the heavy metal removal efficiency and hydraulic residence time requirements of the reactors. Another study used the more typical low-pH mine drainage influent. Experiments also were done to (i) test the effects of oxygen content of feed water on metal removal and (ii) the adsorptive capacity of the reactor organic substrate. Analysis of the results indicates that bacterial sulfate reduction may be a zero-order kinetic reaction relative to sulfate concentrations used in the experiments, and may be the factor that controls the metal mass removal efficiency in the anaerobic treatment systems. The sorptive capacities of the organic substrate used in the experiments had not been exhausted during the experiments as indicated by the loading rates of removal of metals exceeding the mass production rates of sulfide. Microbial sulfate reduction was less in the reactors receiving low-pH influent during experiments with short residence times. Sulfate-reducing bacteria may have been inhibited by high flows of low-pH water. Dissolved oxygen content of the feed waters had little effect on sulfate reduction and metal removal capacity. PMID:12931874

  16. COEUR D'ALENE LAKE, IDAHO. HYPOLIMNETIC CONCENTRATIONS OF DISSOLVED OXYGEN, NUTRIENTS, AND TRACE ELEMENTS, 1987

    EPA Science Inventory

    A reconnaissance study of Coeur dAlene Lake, Idaho (17010303) done from May through November 1987 assessed water quality throughout the lake. Particular emphasis was on hypolimnetic concentrations of dissolved oxygen, nutrients, and trace elements. Study results enabled refinem...

  17. Dissolved and particulate heavy metals distribution in coastal lagoons. A case study from Mar Chiquita Lagoon, Argentina

    NASA Astrophysics Data System (ADS)

    Beltrame, María Ornela; De Marco, Silvia G.; Marcovecchio, Jorge E.

    2009-10-01

    Mar Chiquita Coastal Lagoon is located on the Atlantic coast of Argentina, and it has been declared a Biosphere Reserve under the UNESCO Man and Biosphere Programme (MAB). This coastal lagoon constitutes an estuarine environment with a very particular behaviour and it is ecologically important due to its biological diversity. The aim of the present study was to evaluate the distribution and geochemical behaviour of several heavy metals in this coastal system, focusing on their distribution in both the dissolved phase (<0.45 μm) and the suspended particulate matter. Therefore, the general hydrochemical parameters (salinity, temperature, turbidity, pH and dissolved oxygen) and concentration of total particulate and dissolved metals (Cd, Cu, Ni, Zn, Fe, Pb, Cr and Mn) were measured along 2 years (2004-2006) at two different sites. As regards their distribution, hydrological parameters did not present any evidence of deviation with respect to historical values. Suspended particulate matter showed no seasonal variation or any relationship with the tide, thus indicating that in this shallow coastal lagoon neither tides nor freshwater sources regulate the particulate matter input. Heavy metals behaviour, both in dissolved and particulate phases did not reveal any relationship with tide or seasons. Mar Chiquita Coastal Lagoon showed a large input of dissolved and particulate metals, which is probably due to intensive agriculture within the drainage basin of this system.

  18. The measurement of dissolved and gaseous carbon dioxide concentration

    NASA Astrophysics Data System (ADS)

    Zosel, J.; Oelßner, W.; Decker, M.; Gerlach, G.; Guth, U.

    2011-07-01

    In this review the basic principles of carbon dioxide sensors and their manifold applications in environmental control, biotechnology, biology, medicine and food industry are reported. Electrochemical CO2 sensors based on the Severinghaus principle and solid electrolyte sensors operating at high temperatures have been manufactured and widely applied already for a long time. Besides these, nowadays infrared, non-dispersive infrared and acoustic CO2 sensors, which use physical measuring methods, are being increasingly used in some fields of application. The advantages and drawbacks of the different sensor technologies are outlined. Electrochemical sensors for the CO2 measurement in aqueous media are pointed out in more detail because of their simple setup and the resulting low costs. A detailed knowledge of the basic detection principles and the windows for their applications is necessary to find an appropriate decision on the technology to be applied for measuring dissolved CO2. In particular the pH value and the composition of the analyte matrix exert important influence on the results of the measurements.

  19. 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.

  20. SITE demonstration of the Dynaphore/Forager Sponge technology to remove dissolved metals from contaminated groundwater

    SciTech Connect

    Esposito, C.R.; Vaccaro, G.

    1995-10-01

    A Superfund Innovative Technology Evaluation (SITE) demonstration was conducted of the Dynaphore/Forager Sponge technology during the week of April 3, 1994 at the N.L. Industries Superfund Site in Pedricktown, New Jersey. The Forager Sponge is an open-celled cellulose sponge incorporating an amine-containing chelating polymer that selectively absorbs dissolved heavy metals in both cationic and anionic states. This technology is a volume reduction technology in which heavy metal contaminants from an aqueous medium are concentrated into a smaller volume for facilitated disposal. The developer states that the technology can be used to remove heavy metals from a wide variety of aqueous media, such as groundwater, surface waters and process waters. The sponge matrix can be directly disposed, or regenerated with chemical solutions. For this demonstration the sponge was set up as a mobile pump-and-treat system which treated groundwater contaminated with heavy metals. The demonstration focused on the system`s ability to remove lead, cadmium, chromium and copper from the contaminated groundwater over a continuous 72-hour test. The removal of heavy metals proceeded in the presence of significantly higher concentrations of innocuous cations such as calcium, magnesium, sodium, potassium and aluminum.

  1. Dissolved Divalent Metal and pH Effects on Amino Acid Polymerization: A Thermodynamic Evaluation

    NASA Astrophysics Data System (ADS)

    Kitadai, Norio

    2016-06-01

    Polymerization of amino acids is a fundamentally important step for the chemical evolution of life. Nevertheless, its response to changing environmental conditions has not yet been well understood because of the lack of reliable quantitative information. For thermodynamics, detailed prediction over diverse combinations of temperature and pH has been made only for a few amino acid-peptide systems. This study used recently reported thermodynamic dataset for the polymerization of the simplest amino acid "glycine (Gly)" to its short peptides (di-glycine and tri-glycine) to examine chemical and structural characteristics of amino acids and peptides that control the temperature and pH dependence of polymerization. Results showed that the dependency is strongly controlled by the intramolecular distance between the amino and carboxyl groups in an amino acid structure, although the side-chain group role is minor. The polymerization behavior of Gly reported earlier in the literature is therefore expected to be a typical feature for those of α-amino acids. Equilibrium calculations were conducted to examine effects of dissolved metals as a function of pH on the monomer-polymer equilibria of Gly. Results showed that metals shift the equilibria toward the monomer side, particularly at neutral and alkaline pH. Metals that form weak interaction with Gly (e.g., Mg2+) have no noticeable influence on the polymerization, although strong interaction engenders significant decrease of the equilibrium concentrations of Gly peptides. Considering chemical and structural characteristics of Gly and Gly peptides that control their interactions with metals, it can be expected that similar responses to the addition of metals are applicable in the polymerization of neutral α-amino acids. Neutral and alkaline aqueous environments with dissolved metals having high affinity with neutral α-amino acids (e.g., Cu2+) are therefore not beneficial places for peptide bond formation on the primitive

  2. Investigating extent of dissolved organic carbon stabilization by metal based coagulant in a wetland environment

    NASA Astrophysics Data System (ADS)

    Henneberry, Y.; Mourad, D.; Kraus, T.; Bachand, P.; Fujii, R.; Horwath, W.

    2008-12-01

    This study is part of a larger project designed to investigate the feasibility of using metal-based coagulants to remove dissolved organic carbon (DOC) from island drainage water in the San Joaquin Delta and subsequently retaining the metal-DOC precipitate (floc) in wetlands constructed at the foot of levees to promote levee stability. Dissolved organic carbon is a constituent of concern as some forms of DOC can be converted to carcinogenic compounds during drinking water treatment. The focus of this work is to assess floc stability over time and to determine whether floc can be permanently sequestered as part of wetland sediment. Drainage water collected seasonally from Twitchell Island was coagulated with ferric sulfate and polyaluminum chloride at optimal and 50%-optimal dosage levels. Floc was incubated in the laboratory under anaerobic conditions for six weeks under various conditions including different DOC concentrations, microbial inoculants, and addition of nutrients. Preliminary results indicate the floc is a stable system; little to no DOC was released from the floc into the water column under incubations with native microbial inoculate. In addition, floc incubated with previously coagulated water appeared to remove additional DOC from the water column. Future work will involve field and laboratory studies using 13C labeled plant material to examine the effects of fresh plant matter and the effects of peat soil DOC on floc stability, in order to elucidate mechanisms behind carbon stabilization by metal-based floc.

  3. Metal and phytochelatin content in phytoplankton from freshwater lakes with different metal concentrations

    SciTech Connect

    Knauer, K.; Xue, H.B.; Sigg, L.; Ahner, B.

    1998-12-01

    The trace metal (Cu, Zn, Cd, Mn) and phytochelatin (an intracellular chelator for metal ions) cellular content were determined in phytoplankton samples originating from four lakes. The lakes differ in their metal concentrations and in other conditions (pH, trophic state, organic matter). Total and intracellular contents of Cu and Cd were related to the experimentally determined free metal ion concentration and the total and intracellular content of Mn to the dissolved Mn. The intracellular Zn content was tightly regulated over a broad range of [Zn{sup 2+}]. Phytochelatin concentrations were measurable in phytoplankton communities from three of the lakes, in spite of low levels of free Cu, Zn, and Cd ion concentrations. Culture experiments showed that the concentration of intracellular phytochelatin in Scendesmus subspicatus and in a natural algal community increased upon addition of copper in a similar concentration range as in the lakes. Phytochelatin concentrations were below detection in the phytoplankton collected from the highly contaminated Lake Orta, perhaps suggesting that this algal community has adapted in some other way to high metal concentrations. Although the authors only sampled a few lakes, the lack of any clear relationship between phytochelatin and metal concentrations calls into question the feasibility of using phytochelatins as a bioindicator of metal exposure in lakes.

  4. Use of lichen biomass to monitor dissolved metals in natural waters

    SciTech Connect

    Beck, J.N.; Ramelow, G.J. )

    1990-02-01

    The use of lichens for monitoring airborne metals is based on their immobility and a tendency to accumulate metals to a high degree by the trapping of atmospheric particles and by adsorptive ion exchange processes in which dissolved metals in rainwater are picked up by cellular membranes. The powerful metal-accumulating ability of lichens has been demonstrated in the laboratory. This strong metal accumulating ability of lichen biomass from aqueous solutions would seem to make lichen material an ideal biomonitor of dissolved metals in natural waters. To test this the present study was initiated to monitor dissolved zinc, copper, lead, nickel, cadmium, iron, manganese, chromium, and mercury in an industrially-impacted bayou in southwestern Louisiana. The results obtained with lichen biomonitors will be compared with other studies of the same metals in periphyton and sediments from this waterway.

  5. Effect of dissolved oxygen concentration on iron efficiency: Removal of three chloroacetic acids.

    PubMed

    Tang, Shun; Wang, Xiao-mao; Mao, Yu-qin; Zhao, Yu; Yang, Hong-wei; Xie, Yuefeng F

    2015-04-15

    The monochloroacetic, dichloroacetic and trichloroacetic acid (MCAA, DCAA and TCAA) removed by metallic iron under controlled dissolved 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 concentration. 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 concentration on iron efficiency for contaminant reduction in water and wastewater treatment. PMID:25697696

  6. The effect of solids retention time on dissolved methane concentration in anaerobic membrane bioreactors.

    PubMed

    Yeo, Hyeongu; Lee, Hyung-Sool

    2013-01-01

    We assessed the effect of solids retention times (SRT) on dissolved methane concentration in a lab-scale anaerobic membrane bioreactor (AnMBR) operated at SRT 20d and 40d at ambient temperature (23 +/- 1 degrees C). Daily methane production was 196 +/- 17 mL/d and 285 +/- 18 mL/d for SRT 20d and 40d, respectively. In comparison, the average concentration of dissolved methane in AnMBR permeates was 9.9 +/- 2.3 mg/L for SRT 20d (close to thermodynamic equilibrium), which was decreased to 4.3 +/- 0.3 mg/L for SRT 40d. We often found oversaturation of dissolved methane at SRT 20d, which means that mass transfer of dissolved methane from liquid to gas phase is dynamic at this short SRT. However, we never detected oversaturation of dissolved methane at SRT 40d, due to slow endogenous decay kinetics. Higher daily methane production at SRT 40d than that at SRT 20d indicates that methane was supplementarily produced from biomass electrons by endogenous decay. This study shows that operation of AnMBRs under long SRT can keep low dissolved methane concentration in AnMBR permeate, along with high methane yield. PMID:24350464

  7. 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.

  8. Effect of Dissolved Oxygen Concentration on Development and Hatching of Channel Catfish Ictalurus punctatus Eggs

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Recommendations on required dissolved oxygen (DO) concentrations in channel catfish hatcheries vary widely. This study was conducted to determine effects of DO concentration on development and hatching success of channel catfish eggs. Five channel catfish spawns were collected from a pond at the T...

  9. INCREASED TOXICITY OF AMMONIA TO RAINBOW TROUT 'SALMO GAIRDNERI' RESULTING FROM REDUCED CONCENTRATIONS OF DISSOLVED OXYGEN

    EPA Science Inventory

    The median lethal concentration (LC50) of aqueous ammonia at reduced dissolved oxygen (D.O.) concentrations was tested in acute toxicity tests with rainbow trout (Salmo gairdneri) fingerlings. Fifteen 96-h flow-through tests were conducted over the D.O. range 2.6-8.6 mg/L, the fo...

  10. Production Responses of Channel Catfish to Minimum Daily Dissolved Oxygen Concentrations in Earthen Ponds

    Technology Transfer Automated Retrieval System (TEKTRAN)

    The purpose of this study was to determine the effects of the minimum daily dissolved oxygen (DO) concentration on production parameters of channel catfish Ictalurus punctatus in earthen ponds. Fifteen one-acre ponds (5 ponds per treatment) were managed as High Oxygen (minimum DO concentrations aver...

  11. Effect of daily minimum pond dissolved oxygen concentration on hybrid striped bass fingerling yield

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Management of dissolved oxygen (DO) concentration in ponds at night during the growing season is important because fish growth and yield are greater in ponds with higher nightly DO concentrations. The purpose of this study was to quantify the production and water quality responses of hybrid striped ...

  12. Distribution of dissolved and particulate trace metals in Arctic sea ice

    NASA Astrophysics Data System (ADS)

    Taylor, M.; Hendy, I. L.; Aciego, S.; Meyer, K.

    2014-12-01

    Iron (Fe) is an essential biolimiting micronutrient, however, the bioavailablility of Fe is dependent on source and speciation. In a high nutrient/low chlorophyll region of the ocean such as the Arctic, sea ice is an important aggregator of dissolved and particulate Fe from aerosol, lithogenic, and biogenic sources. While particulate Fe is less bioavailable than dissolved Fe, it is far more abundant in sea ice. As a result, sea ice directly enhances productivity by ice entrapment of mineral dust particulates containing Fe, which can be released into the surface ocean waters during melting. In seawater underlying sea ice, Fe can be concentrated up to two orders of magnitude higher than in the ice-free open ocean (Lannuzel et al., 2011). A transect of sea ice cores were collected in the spring of 2014 offshore of Barrow, AK, and the Canadian Arctic Archipelago to capture a gradient of sediment contributions from shelf sediments to aeolian sediments. At Barrow, AK, land fast first year ice was sampled. In the Canadian Arctic, both multi-year (pack ice) and first year (land fast) ice cores were retrieved. First year ice cores were between 100-150 cm thick and the multi year core was 195 cm thick. Cores were subsampled by depth and filtered. The resulting ice core sediments were analyzed for elemental composition, and multistep Fe-leaching experiments were conducted to determine the fraction of soluble Fe. Thus we have ascertained the solubility of particulate Fe prior to onset of melt season. Dissolved trace metals were also analyzed to ascertain changes in concentration with ice core depth of lithogenic elements (Mn, Al) and biologically important elements (Si, Mo, Cu, Zn). Preliminary results show some enrichment of lithogenic inputs near surface, indicating dust deposition, and lower portions of the cores, suggesting resuspended sediments from the continental shelf. Concentrations of some biologically important elements decrease with depth, suggesting possible

  13. Monitoring dissolved copper concentrations in Chesapeake Bay, U.S.A.

    PubMed

    Hall, W S; Bushong, S J; Hall, L W; Lenkevich, M J; Pinkney, A E

    1988-07-01

    Dissolved copper and selected water chemistry parameters were monitored for 11 months in Chesapeake Bay, U.S.A. Dissolved copper concentrations in four recreational marinas, a large harbor, two major river systems, and a heavily used shipping canal ranged from below detectable levels to 80 μg L(-1) (\\-X=11.7 μg L(-1)). Dissolved copper was detected >91% of the time at five locations. Lowest copper concentrations were found in Potomac River, Baltimore Harbor, Pier One Marina, and C & D Canal (\\-X=6-10 μg L(-1); slightly higher levels of dissolved copper were found in Choptank River (\\-X=12 μg L(-1)). Highest levels of copper were detected in Port Annapolis, Hartge, and Piney Narrows Marinas (\\-X=13-18 μg L(-1)), with the highest values observed in the study (70 and 80 μg L(-1)) found in two of these marinas. Copper in the three marinas with highest dissolved copper levels could have been toxic to some of the more sensitive aquatic species. Intensive study of one marina indicated that a likely source of dissolved copper was the recreational boats housed in the marina. PMID:24248797

  14. 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.

  15. 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.

  16. Dissolved and labile concentrations 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

    USGS Publications Warehouse

    Balistrieri, L.S.; Blank, R.G.

    2008-01-01

    In order to evaluate thermodynamic speciation calculations inherent in biotic ligand models, the speciation of dissolved 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 dissolved metals and concentrations of metal associated with biotic ligands (e.g., fish gills). Maximum dynamic metal concentrations, determined from total dissolved metal concentrations and thermodynamic speciation calculations, are compared with labile metal concentrations 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 concentrations of Cd and Zn associated with biotic ligands for geochemical conditions in the study area, whereas concentrations 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 concentrations and dynamic metal concentrations 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 concentrations of multiple metals should incorporate analytical speciation methods, such as DGT, to constrain the speciation component of biotic ligand models. ?? 2008 Elsevier Ltd.

  17. User's manual for estimation of dissolved-solids concentrations and loads in surface water

    USGS Publications Warehouse

    Liebermann, T.D.; Middelburg, R.F.; Irvine, S.A.

    1987-01-01

    Dissolved solids in surface water are an important indicator of overall water quality. Ordinarily, dissolved-solids concentrations and loads are estimated by indirect methods that are based on periodic chemical analyses. Three computer programs , FLAGIT, DVCOND, and SLOAD, were developed to provide a consistent and accurate method of estimating dissolved-solids concentrations and loads. FLAGIT retrieves daily values of specific conductance and discharge and periodic water quality analyses from the U.S. Geologic Survey 's National Water Data Storage and Retrieval System data base, deletes incomplete data, and flags possible data errors. DVCOND fills in missing daily values of specific conductance, when appropriate, by linear interpolation. Using water quality data, SLOAD computes 3 yr moving regressions of dissolved-solids loads as a function of specific conductance and discharge. SLOAD then applies the regression coefficients to the daily values data to estimate daily dissolved-solids loads that are summed by month and by year. Separate regressions are used to estimate the mass fractions of six major ions. The theoretical basis and underlying assumptions of the procedures are presented, with documentation of the programs and their use. (USGS)

  18. 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).

  19. Declines in Dissolved Silica Concentrations in Western Virginia Streams (1988- 2003)

    NASA Astrophysics Data System (ADS)

    Grady, A. E.; Scanlon, T. M.; Galloway, J. N.

    2006-12-01

    Dissolved silica concentrations in western Virginia streams showed a significant bias toward declines (p<0.0001) over the time period from 1988-2003. Streams with the greatest declines were those that had the highest mean dissolved silica concentrations, specific to watersheds underlain by basaltic and granitic bedrock. We examined potential geochemical, hydrological, and biological factors that could account for the observed widespread declines, focusing on six core watersheds where weekly stream chemistry data were available. No relationships were evident between stream water dissolved silica concentrations and pH, a finding supported by the results from a geochemical model applied to the dominant bedrock mineralogy. Along with changes in watershed acidity, changes in precipitation and discharge were also discounted since no significant trends were observed over the study period. Analyses of two longer-term datasets that extend back to 1979 revealed that the initiation of the dissolved silica declines coincided with the timing of a gypsy moth (Lymantria dispar) defoliation event. We develop a conceptual model centered on benthic diatoms, which are found within each of the six core watersheds but in greater abundance in the more silica-rich streams. Gypsy moth defoliation lead to greater sunlight penetration and enhanced nitrate concentrations in the streams, which could have spurred population growth and silica uptake. The model can explain why the observed declines are primarily driven by decreased concentrations during low-flow conditions. This study illustrates lasting effects of disturbance on watershed biogeochemistry, in this case causing decadal-scale variability in stream water dissolved silica concentrations.

  20. 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

  1. Method of dissolving metal oxides with di- or polyphosphonic acid and a redundant

    DOEpatents

    Horwitz, Earl P.; Chiarizia, Renato

    1996-01-01

    A method of dissolving metal oxides using a mixture of a di- or polyphosphonic acid and a reductant wherein each is present in a sufficient amount to provide a synergistic effect with respect to the dissolution of metal oxides and optionally containing corrosion inhibitors and pH adjusting agents.

  2. Occurrence and concentration of dissolved silver in rivers in England and Wales.

    PubMed

    Peters, A; Simpson, P; Merrington, G; Rothenbacher, K; Sturdy, L

    2011-06-01

    There is a paucity of monitoring data for silver in freshwater environments in Europe. There are several reasons for this, including the relatively low levels of silver in the aquatic environment and the requirement for commensurately low levels of detection (<100 ng l⁻¹), which are generally not routinely achieved in analytical laboratories. In this study 425 separate analytical determinations for dissolved (<0.45 μm) silver from 84 Environment Agency monitoring stations were carried out. Sampling was carried out on a monthly basis over a period of 6 months. Of the 425 samples, 346 were reported as having dissolved silver concentrations below the limit of quantification (6.6 ng l⁻¹) and, of these, 280 samples were reported as below the reporting limit of detection (3 ng l⁻¹). The mean of the maximum dissolved silver concentrations reported at each station was calculated as 6.1 ng l⁻¹ using a statistical extrapolation technique to allow for the high level of censorship in the dataset. The maximum mean dissolved silver concentration recorded at a station was 19.8 ng l⁻¹. A freshwater Predicted No Effect Concentration (PNEC) of 40 ng l⁻¹ was used in this study. PMID:21516451

  3. 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, ...

  4. Magnetic sulfide-modified nanoscale zerovalent iron (S-nZVI) for dissolved metal ion removal.

    PubMed

    Su, Yiming; Adeleye, Adeyemi S; Keller, Arturo A; Huang, Yuxiong; Dai, Chaomeng; Zhou, Xuefei; Zhang, Yalei

    2015-05-01

    Sulfide-modified nanoscale zerovalent iron (S-nZVI) is attracting a lot of attention due to its ease of production and high reactivity with organic pollutants. However, its structure is still poorly understood and its potential application in heavy metal remediation has not been explored. Herein, the structure of S-nZVI and its cadmium (Cd) removal performance under different aqueous conditions were carefully investigated. Transmission electron microscopy (TEM) with an energy-dispersive X-ray spectroscopy (EDS) analysis suggested that sulfur was incorporated into the zerovalent iron core. Scanning electron microscopy (SEM) with EDS analysis demonstrated that sulfur was also homogeneously distributed within the nanoparticles. When the concentration of Na2S2O4 was increased during synthesis, a flake-like structure (FeSx) increased significantly. S-nZVI had an optimal Cd removal capacity of 85 mg/g, which was >100% higher than for pristine nZVI. Even at pH 5, over 95% removal efficiency was observed, indicating sulfide compounds played a crucial role in metal ion removal and particle chemical stability. Oxygen impaired the structure of S-nZVI but enhanced Cd removal capacity to about 120 mg/g. Particle aging had no negative effect on removal capacity of S-nZVI, and Cd-containing mixtures remained stable in a two months experiment. S-nZVI can efficiently sequester dissolved metal ions from different contaminated water matrices. PMID:25706223

  5. Significance of groundwater discharge along the coast of Poland as a source of dissolved metals to the southern Baltic Sea.

    PubMed

    Szymczycha, Beata; Kroeger, Kevin D; Pempkowiak, Janusz

    2016-08-15

    Fluxes of dissolved trace metals (Cd, Co, Cr, Cu, Mn, Ni, Pb, and Zn) via groundwater discharge along the southern Baltic Sea have been assessed for the first time. Dissolved metal concentrations in groundwater samples were less variable than in seawater and were generally one or two orders of magnitude higher: Cd (2.1-2.8nmolL(-1)), Co (8.70-8.76nmolL(-1)), Cr (18.1-18.5nmolL(-1)), Mn (2.4-2.8μmolL(-1)), Pb (1.2-1.5nmolL(-1)), Zn (33.1-34.0nmolL(-1)). Concentrations of Cu (0.5-0.8nmolL(-1)) and Ni (4.9-5.8nmolL(-1)) were, respectively, 32 and 4 times lower, than in seawater. Groundwater-derived trace metal fluxes constitute 93% for Cd, 80% for Co, 91% for Cr, 6% for Cu, 66% for Mn, 4% for Ni, 70% for Pb and 93% for Zn of the total freshwater trace metal flux to the Bay of Puck. Groundwater-seawater mixing, redox conditions and Mn-cycling are the main processes responsible for trace metal distribution in groundwater discharge sites. PMID:27293076

  6. Dissolved trace element concentrations in the East River-Long Island Sound system: relative importance of autochthonous versus allochthonous sources.

    PubMed

    Buck, Nathaniel J; Gobler, Christopher J; Sañudo-Wilhelmy, Sergio A

    2005-05-15

    Dissolved trace metal (Ag, Cd, Cu, Fe, Ni, Pb, and Zn), inorganic nutrient (NO3, NH4, PO4, H4SiO4), and DOC concentrations were measured at 43 stations during low (July 2000) and high (April 2001) river discharge conditions in surface waters of Long Island Sound (LIS). To evaluate the impact of fluvial sources to the total metal budget of the sound, samples were collected from major tributaries discharging into LIS (Thames, Quinnipiac, Housatonic, Connecticut, and East Rivers). To compare LIS with other coastal embayments, samples were also collected from five LIS coastal embayments (Manhassett Bay, Huntington Harbor, Oyster Bay, Hempstead Harbor, and Port Jefferson Harbor), which are monitored by the U.S. National Status and Trends Program. Metal and nutrient distributions identified two biogeochemical regimes within LIS: an area of relatively high nutrient and metal concentrations in the East River/Narrows region in western LIS and an area in the eastern region of the sound that had comparatively lower concentrations. Mass balance estimates indicated that, during low flow conditions, the East River was the dominant allochthonous source of most trace metals (Ag, Cd, Cu, Ni, Zn) and inorganic nutrients (NO3 and PO4); during high flow conditions, the most influential source of these constituents was the Connecticut River. Mass balance estimates also evidenced a large autochthonous source of Cu, Ni, and Zn, as their spatial distributions displayed elevated concentrations away from point sources such as the East River. Principal component analysis suggested that metal and nutrient distributions in the LIS system were influenced by different seasonal processes: remobilization from contaminated sediments, anthropogenic inputs from sewage discharges and phytoplankton scavenging during the spring freshet, and benthic remobilization during summer conditions. PMID:15952355

  7. Nonaqueous method for dissolving lanthanide and actinide metals

    DOEpatents

    Crisler, L.R.

    1975-11-11

    Lanthanide and actinide beta-diketonate complex molecular compounds are produced by reacting a beta-diketone compound with a lanthanide or actinide element in the elemental metallic state in a mixture of carbon tetrachloride and methanol.

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

    USGS Publications Warehouse

    Lum, W. E., II; 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)

  9. Concentrations of dissolved and particulate Polychlorinated Biphenyls in water from the Saginaw River, Michigan

    USGS Publications Warehouse

    Verbrugge, David A.; Giesy, John P.; Mora, Miguel A.; Williams, Lisa L.; Rossmann, Ronald; Moll, Russell A.; Tuchman, Marc

    1995-01-01

    The Saginaw River receives water from a major drainage basin in the east-central portion of the lower peninsula of Michigan. Historically the river has been contaminated with polychlorinated biphenyls (PCBs) from several sources. The present study was conducted to determine the concentrations of PCBs in both the dissolved and particulate phases of water in the lower Saginaw River, as well as the relative contribution of PCBs from the lower portion of the river relative to more upstream locations. Water samples were collected in 1990–1991, during a range of discharge conditions. Suspended particulates were collected from water onto glass-fiber filters by use of a “Penta-plate” filtration apparatus. Filtered water was subsequently passed through XAD-2 macroreticular resin to collect the “dissolved” PCBs. Concentrations of PCBs in both phases were determined by congener specific gas chromatography with electron capture detection. Total concentrations of PCBs ranged from 11 to 31 ng/L. The concentrations of PCBs in the dissolved phase ranged from 1.9 to 16 ng/L. The ratio of total PCBs bound to suspended particulates, relative to dissolved PCBs, was 2:1 and remained fairly constant for discharges less than approximately 400 M3/sec. The loading of total PCBs to Saginaw Bay was estimated to be 225 kg/yr, of which approximately 60% was found to be contributed by the lower 8 km of the Saginaw River.

  10. New Concentric Electrode Metal-Semiconductor-Metal Photodetectors

    NASA Technical Reports Server (NTRS)

    Towe, Elias

    1996-01-01

    A new metal-semiconductor-metal (MSM) photodetector geometry is proposed. The new device has concentric metal electrodes which exhibit a high degree of symmetry and a design flexibility absent in the conventional MSM device. The concentric electrodes are biased to alternating potentials as in the conventional interdigitated device. Because of the high symmetry configuration, however, the new device also has a lower effective capacitance. This device and the conventional MSM structure are analyzed within a common theoretical framework which allows for the comparison of the important performance characteristics.

  11. Dissolved Rare Earth Element Concentrations in the Upwelling area off Peru

    NASA Astrophysics Data System (ADS)

    Grasse, P.; Plass, A.; Hathorne, E. C.; Frank, M.

    2012-12-01

    Rare earth elements (REEs) are powerful tracers of continental input, particle exchange and scavenging processes, as well as for water mass transport in the ocean. We present a first data set of dissolved REE distributions in filtered seawater covering the major gradients of bio-productivity and oxygen concentrations in the upwelling area off Peru. A total of 22 stations were analyzed along a shelf, a nearshore and an offshore transect to investigate the influence of local inputs versus water mass mixing. The Peruvian coastal upwelling area is a highly dynamic system characterized by intense upwelling of nutrient-rich subsurface water and therefore high productivity that leads to one of the globally largest Oxygen Minimum Zones (OMZ). The upwelling area off Peru is of particular interest for understanding the biogeochemical cycling of REEs and other redox-sensitive metals because anoxic conditions are expected to release of REEs from the shelf, whereas high particle densities and fluxes efficiently remove the REEs from the water column. Despite their high potential as tracers few systematic investigations of seawater REEs have been carried out so far because the low concentrations of REEs (pM) are difficult to measure. In this study an online preconcentration (OP) system (seaFast, Elemental Scientific Inc.) was used with a technique slightly modified from Hathorne et al. (2012). The OP system efficiently separates seawater matrix elements from the REEs and elutes the preconcentrated sample directly into the spray chamber of the ICP-MS instrument. Repeated measurements of a seawater reference sample (n= 20) during this study gave a reproducibility of between 5% and 15% (2σ), with the worst reproducibility for Sm, Eu, and Gd (12% to 15%). In general, the REEs, except Ce, show a nutrient-like behavior in seawater increasing in concentration with water depth. However, such distributions were not observed for some stations on the shelf where the highest concentrations

  12. Statistical models for estimating seawater metal concentrations from metal concentrations in mussels (Mytilus edulis)

    SciTech Connect

    Popham, J.D.; D'Auria, J.M.

    1981-12-01

    The report presents the regression coefficients of models for estimating the copper, zinc and lead concentrations in seawater based upon the metal concentrations in mussels along with their accuracy and reliability.

  13. 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.

  14. Characterization of dissolved organic matter from a restored urban marsh and its role in the mobilization of trace metals.

    PubMed

    ElBishlawi, Hagar; Jaffe, Peter R

    2015-05-01

    Dissolved organic matter (DOM), although highly variable and not very well characterized, plays a role in many important environmental reaction and transport processes, including trace metal mobilization. This study characterizes heterogeneous DOM from the pore-water of a restored urban tidal marsh, using chemical, optical, and electrochemical methods for dissolved organic carbon/nitrogen ratios (C:N: 1.8-6.4), spectroscopic characteristics (decreased aromaticity in amended sediments), element ratios (maximum sediment-associated trace metal concentrations measured<30 cm), and metal complexation properties (logKc: Cd: 10.7±0.7>Pb: 9.5±0.1>Cr: 7.3±0.1>Cu: 5.07±0.53), all as a function of sediment depth. Specific DOM properties from the restored marsh were then compared to pore-water samples from a natural marsh and a simulated wetland microcosm which resulted in similar values, while the reference humic acid significantly differed in properties from field DOM. The results revealed that reference humic acids do not accurately represent the complexity of natural heterogeneous DOM, whereas a simulated wetland microcosm may provide a reasonable representation of natural DOM. Clear differences between amended and original soil (transition below 30 cm) were observed in DOM and trace metal properties including: lower DOM content, higher logKc values, less DOM complexity, development of a iron-sulfide redox buffering pool, and greater affinity for metals in the solid phase occurring in the amended sediments. PMID:25681788

  15. Composition, removal, redox, and metal complexation properties of dissolved organic nitrogen in composting leachates.

    PubMed

    He, Xiao-Song; Xi, Bei-Dou; Zhang, Zong-Yong; Gao, Ru-Tai; Tan, Wen-Bing; Cui, Dong-Yu; Yuan, Ying

    2015-01-01

    This study investigated the composition, removal, redox, and metal complexation characteristics of dissolved organic nitrogen (DON) in composting leachates. Results showed that the leachate-derived DON comprised proteinaceous compounds and amines, and most of them were integrated into the fulvic- and humic-like substances. Neutral, basic, acidic, hydroxylic, aromatic, and sulfuric amino acids all were detected in the influent leachates. However, most of them were removed by the biological and physical processes, and only neutral amino acids were detected in the effluent. The DON was not the main contributor to the redox capability of the leachate dissolved organic matter (DOM). However, it exhibited a strong capability for metal complexation. The amines formed strong complexes with the metals Mo, Co, Cr, and Ni, while the proteinaceous matter interacted with the metals Cr and Ni. PMID:25282175

  16. Impact of solute concentration on the electrocatalytic conversion of dissolved gases in buffered solutions

    NASA Astrophysics Data System (ADS)

    Shinagawa, Tatsuya; Takanabe, Kazuhiro

    2015-08-01

    To maintain local pH levels near the electrode during electrochemical reactions, the use of buffer solutions is effective. Nevertheless, the critical effects of the buffer concentration on electrocatalytic performances have not been discussed in detail. In this study, two fundamental electrochemical reactions, oxygen reduction reaction (ORR) and hydrogen oxidation reaction (HOR), on a platinum rotating disk electrode are chosen as model gas-related aqueous electrochemical reactions at various phosphate concentrations. Our detailed investigations revealed that the kinetic and limiting diffusion current densities for both the ORR and HOR logarithmically decrease with increasing solute concentration (log |jORR | = - 0.39 c + 0.92 , log |jHOR | = - 0.35 c + 0.73) . To clarify the physical aspects of this phenomenon, the electrolyte characteristics are addressed: with increasing phosphate concentration, the gas solubility decrease, the kinematic viscosity of the solution increase and the diffusion coefficient of the dissolved gases decrease. The simulated limiting diffusion currents using the aforementioned parameters match the measured ones very well (log |jORR | = - 0.43 c + 0.99 , log |jHOR | = - 0.40 c + 0.54) , accurately describing the consequences of the electrolyte concentration. These alterations of the electrolyte properties associated with the solute concentration are universally applicable to other aqueous gas-related electrochemical reactions because the currents are purely determined by mass transfer of the dissolved gases.

  17. Urban Impact of Dissolved Metals in the Paso del Norte Segment of the Rio Grande

    ERIC Educational Resources Information Center

    Freiwan, Sumayeh Ahmad

    2013-01-01

    The Paso del Norte segment of the Rio Grande experiences two seasons per year; the (wet) irrigation season and the (dry) non-irrigation season. The goal of this study was to improve the understanding of occurrence and contribution of dissolved metals in this region during the non-irrigation season. The objectives of this study were to (1) evaluate…

  18. Spatial variation in concentrations of dissolved nitrogen species in an upland blanket peat catchment.

    PubMed

    Cundill, A P; Chapman, P J; Adamson, J K

    2007-02-01

    The concentration of nitrogen (N), particularly as nitrate (NO3-N), in upland streams, lakes and rivers is frequently used as a diagnostic of the vulnerability of upland ecosystems to increased atmospheric nitrogen deposition and N saturation. The N content of running waters, however, is generally assessed on the basis of sampling at a limited number of points in space and time within the catchment under investigation. The current study was conducted at Trout Beck, an 11.5 km2 blanket peat-dominated catchment in the North Pennine uplands of the UK. Results from sampling at 33 sites within this catchment demonstrated that the concentrations of all dissolved N species were highly variable, even over short distances. Statistical relationships between the concentrations of NO3-N and dissolved organic nitrogen (DON) and percentage catchment cover of Calluna/Eriophorum and Eriophorum vegetation were found. However, it was also noted that in catchments containing limestone outcrops, NO3-N concentration was much higher than in catchments where runoff was sourced directly from the blanket peat surface. It is possible that NH4-N and DON leached from the blanket peat are mineralised and nitrified, providing a source for the NO3-N found in the river channels. Overall, the current study suggests that interpretations of N-saturation based on river water chemistry measurements at a single point must be treated cautiously, and that the influence of catchment-scale physical factors, such as vegetation and geology cover on the concentration of dissolved N species in upland river waters should not be ignored. PMID:17182088

  19. Influence of dissolved organic matter on photogenerated reactive oxygen species and metal-oxide nanoparticle toxicity.

    PubMed

    Li, Yang; Niu, Junfeng; Shang, Enxiang; Crittenden, John Charles

    2016-07-01

    The effect of humic acid (HA) or fulvic acid (FA) on reactive oxygen species (ROS) generation by six metal-oxide nanoparticles (NPs) and their toxicities toward Escherichia coli was investigated under UV irradiation. Dissolved organic matter (DOM) decreased OH generation by TiO2, ZnO, and Fe2O3, with FA inhibiting OH generation more than HA. The generated OH in NPs/DOM mixtures was higher than the measured concentrations because DOM consumes OH faster than its molecular probe. None of NPs/FA mixtures produced O2(-). The generated O2(-) concentrations in NPs/HA mixtures (except Fe2O3/HA) were higher than the sum of O2(-) concentrations that produced as NPs and HA were presented by themselves. Synergistic O2(-) generation in NPs/HA mixtures resulted from O2 reduction by electron transferred from photoionized HA to NPs. DOM increased (1)O2 generation by TiO2, CuO, CeO2, and SiO2, and FA promoted (1)O2 generation more than HA. Enhanced (1)O2 generation resulted from DOM sensitization of NPs. HA did not increase (1)O2 generation by ZnO and Fe2O3 primarily because released ions quenched (1)O2 precursor ((3)HA*). Linear correlation was developed between total ROS concentrations generated by NPs/DOM mixtures and bacterial survival rates (R(2) ≥ 0.80). The results implied the necessity of considering DOM when investigating the photoreactivity of NPs. PMID:27064207

  20. Size exclusion and anion exchange high performance liquid chromatography for characterizing metals bound to marine dissolved organic matter.

    PubMed

    García-Otero, Natalia; Bermejo-Barrera, Pilar; Moreda-Piñeiro, Antonio

    2013-01-14

    Size exclusion chromatography (SEC) followed by anion exchange chromatography (AEC) hyphenated with inductively coupled plasma-mass spectrometry (ICP-MS) was applied for fractionating metals bound to marine dissolved organic matter (DOM). Surface seawater samples (100 L) were subjected to tangential flow ultrafiltration (10,000 Da cut off) for isolating and pre-concentrating dissolved large molecules. The isolated fraction (retentate) consisted of 1L, which was further freeze-dried and re-dissolved to 250 mL with ultrapure water. After HI Trap desalting of the re-dissolved retentate, SEC with UV detection showed marine DOM ranging from 6.5 kDa (lower than the permeable volume of the SEC column) to 16 kDa. A further characterization of this fraction by AEC with UV detection revealed the existence of four groups of macromolecules exhibiting retention times of 2.3, 2.8, 4.5 and 14.0 min. AEC hyphenated with ICP-MS showed the presence of strontium and zinc in the first AE fraction isolated from the SEC fraction; while manganese was found to be bound to the second AE fraction. Cobalt was found to be bound to molecules comprising the third AE fraction. PMID:23265737

  1. Naturally dissolved arsenic concentrations in the Alpine/Mediterranean Var River watershed (France).

    PubMed

    Barats, Aurélie; Féraud, Gilbert; Potot, Cécile; Philippini, Violaine; Travi, Yves; Durrieu, Gaël; Dubar, Michel; Simler, Roland

    2014-03-01

    A detailed study on arsenic (As) in rocks and water from the Var River watershed was undertaken aiming at identifying (i) the origin and the distribution of As in this typical Alpine/Mediterranean basin, and (ii) As input into the Mediterranean Sea. Dissolved As concentrations in the Var River range from 0.1 to 4.5 μg⋅L(-1), due to high hydrological variability and the draining through different geological formations. In the upper part of the Var drainage basin, in the Tinée and the Vésubie valleys, high levels of dissolved As concentrations occur (up to 263 μg⋅L(-1)). The two main sources of As in rocks are the Hercynian metamorphic rocks and the Permian argilites. Highly heterogeneous distribution of As in waters draining through metamorphic rocks is probably related to ore deposits containing arsenopyrite. As, U, W and Mo concentrations in water and rocks correspond to the formation of As-rich ore deposits around Argentera granite by hydrothermal fluids deposited at the end of the Hercynian chain formation, which occurred about 300 My ago. In 2009, weekly monitoring was performed on the Var River (15 km upstream of the mouth), highlighting an average dissolved As concentration (<0.45 μm) of 2.7 ± 0.9 μg⋅L(-1), which is significantly higher than the world-average baseline for river water (0.83 μg⋅L(-1)). Taking the average annual discharge (49.4 m(3)⋅s(-1)) into account and the As levels in the dissolved phase and in deposits of the Var River, dissolved As input into the Mediterranean Sea would be 4. 2± 1.4 tons⋅year(-1) which represents 59% of the total As flux. This study also reveals a probable non-conservative As behaviour, i.e., possible transfer between aqueous and solid phases, during the mixing of the Var River with a tributary. PMID:24388820

  2. The Distribution between the Dissolved and the Particulate Forms of 49 Metals across the Tigris River, Baghdad, Iraq

    PubMed Central

    Hamad, Samera Hussein; Schauer, James Jay; Shafer, Martin Merrill; Abed Al-Raheem, Esam; Satar, Hyder

    2012-01-01

    The distribution of dissolved and particulate forms of 49 elements was investigated along transect of the Tigris River (one of the major rivers of the world) within Baghdad city and in its major tributary (Diyala River) from 11 to 28 July 2011. SF-ICP-MS was used to measure total and filterable elements at 17 locations along the Tigris River transect, two samples from the Diyala River, and in one sample from the confluence of the two rivers. The calculated particulate forms were used to determine the particle-partition coefficients of the metals. No major changes in the elements concentrations down the river transect. Dissolved phases dominated the physical speciation of many metals (e.g., As, Mo, and Pt) in the Tigris River, while Al, Fe, Pb, Th, and Ti were exhibiting high particulate fractions, with a trend of particle partition coefficients of [Ti(40) > Th(35) > Fe(15) > Al(13) > Pb(4.5)] ∗ 106 L/kg. Particulate forms of all metals exhibited high concentrations in the Diyala River, though the partition coefficients were low due to high TSS (~270 mg/L). A comparison of Tigris with the major rivers of the world showed that Tigris quality in Baghdad is comparable to Seine River quality in Paris. PMID:23304083

  3. 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.

  4. The capacity of biochar made from common reeds to neutralise pH and remove dissolved metals in acid drainage.

    PubMed

    Mosley, Luke M; Willson, Philip; Hamilton, Benjamin; Butler, Greg; Seaman, Russell

    2015-10-01

    We tested the capacity of biochar (made at 450 °C from a common reed species) to neutralise pH and remove metals in two acid drainage waters (pH 2.6 and 4.6) using column leaching and batch mixing experiments. In the column experiments, the acid drainage water was neutralised upon passage through the biochar with substantial increases (4-5 pH units) in the leachate pH. In the batch experiments, the leachate pH remained above 6.5 when the drainage:biochar ratio was less than approximately 700:1 (L acid drainage:kg biochar) and 20:1 for the pH 4.6 and pH 2.6 drainage waters, respectively. Dissolved metal concentrations were reduced by 89-98 % (Fe ≈ Al > Ni ≈ Zn > Mn) in the leachate from the biochar. A key mechanism of pH neutralisation appears to be solid carbonate dissolution as calcite (CaCO3) was identified (via X-ray diffraction) in the biochar prior to contact with acid drainage, and dissolved alkalinity and Ca was observed in the leachate. Proton and metal removal by cation exchange, direct binding to oxygen-containing functional groups, and metal oxide precipitation also appears important. Further evaluation of the treatment capacity of other biochars and field trials are warranted. PMID:26004563

  5. Enhanced multi-metal extraction with EDDS of deficient and excess dosages under the influence of dissolved and soil organic matter.

    PubMed

    Yan, Dickson Y S; Lo, Irene M C

    2011-01-01

    This study investigated the influence of dissolved and soil organic matter on metal extraction from an artificially contaminated soil. With high concentration of DOM, the extraction of Cu, Zn and Pb was enhanced by forming additional metal-EDDS complexes under EDDS deficiency. However, the enhancement of metal extraction under EDDS excess was probably due to the soil structure being disrupted owing to humic acid enhanced Al and Fe dissolution, which induced more metals dissolving from the soils. Fulvic acid was found to enhance metal extraction to a greater extent compared with humic acid because of its high content of the carboxylic functional group. Cu extraction from the soil with high organic matter content using EDDS was the lowest due to the high binding affinity of Cu to SOM, whereas Zn extraction became the highest because of a preference for EDDS to extract Zn due to the high stability constant of ZnEDDS. PMID:20970231

  6. Rheological behaviors in the regimes from dilute to concentrated in cellulose solutions dissolved at low temperature.

    PubMed

    Lue, Ang; Zhang, Lina

    2009-05-13

    Cellulose was dissolved rapidly in 9.5 wt.-% NaOH/4.5 wt.-% thiourea aqueous solution pre-cooled to -5 degrees C to prepare cellulose solution with different concentrations. The rheological properties of the cellulose solutions in wide concentration regimes from dilute (0.008 wt.-%) to concentrated (4.0 wt.-%) at 25 degrees C were investigated. On the basis of data from the steady-shear flow test, the critical overlap (c*), the entanglement (c(e)) and the gel (c(g)) concentrations of the cellulose solution at 25 degrees C were determined, respectively, to be 0.10 wt.-%, 0.53 wt.-% and 2.50 wt.-%, in accordance with the results of storage modulus (G') versus c by dynamic test. Moreover, the Cox-Merz deviation at relatively low concentrations was in good agreement with the micro-gel particles in dilute regime. As the cellulose concentration increased, a homogeneous 3-dimensional network formed in the cellulose solution in the concentrated regime, and further increasing of the concentration led to micro-phase separation as determined by the time-temperature superposition (tTS). So far, this complex cellulose solution has been successfully described by the concentration regime theory for the first time, and the relatively molecular morphologies in each regime have been determined, providing useful information for the applications of the cellulose solution systems. PMID:19039777

  7. Cooperative interactions of metal nanoparticles in the ion-exchange matrix with oxygen dissolved in water

    NASA Astrophysics Data System (ADS)

    Khorolskaya, S. V.; Polyanskii, L. N.; Kravchenko, T. A.; Konev, D. V.

    2014-06-01

    The kinetics of the reduction of molecular oxygen dissolved in water with nanocomposites consisting of an ion-exchange matrix and copper nanoparticles deposited in it in various amounts was studied. As the metal content in the polymer increased, the amount of reduced oxygen initially increased and then reached the limiting value. At a certain metal content, ionization of individual particles with formation of metal counterions changes to the oxidation of particles assembly giving layers of oxide products. The mechanism changes at the percolation threshold of the electron conductivity of the nanocomposite and determines the maximum amount of absorbed oxygen.

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

    USGS Publications Warehouse

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

    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

  9. Dissolved and particulate trace metal micronutrients under the McMurdo Sound seasonal sea ice: basal sea ice communities as a capacitor for iron

    PubMed Central

    Noble, Abigail E.; Moran, Dawn M.; Allen, Andrew E.; Saito, Mak A.

    2013-01-01

    Dissolved and particulate metal concentrations are reported from three sites beneath and at the base of the McMurdo Sound seasonal sea ice in the Ross Sea of Antarctica. This dataset provided insight into Co and Mn biogeochemistry, supporting a previous hypothesis for water column mixing occurring faster than scavenging. Three observations support this: first, Mn-containing particles with Mn/Al ratios in excess of the sediment were present in the water column, implying the presence of bacterial Mn-oxidation processes. Second, dissolved and labile Co were uniform with depth beneath the sea ice after the winter season. Third, dissolved Co:PO3−4 ratios were consistent with previously observed Ross Sea stoichiometry, implying that over-winter scavenging was slow relative to mixing. Abundant dissolved Fe and Mn were consistent with a winter reserve concept, and particulate Al, Fe, Mn, and Co covaried, implying that these metals behaved similarly. Elevated particulate metals were observed in proximity to the nearby Islands, with particulate Fe/Al ratios similar to that of nearby sediment, consistent with a sediment resuspension source. Dissolved and particulate metals were elevated at the shallowest depths (particularly Fe) with elevated particulate P/Al and Fe/Al ratios in excess of sediments, demonstrating a sea ice biomass source. The sea ice biomass was extremely dense (chl a >9500 μg/L) and contained high abundances of particulate metals with elevated metal/Al ratios. A hypothesis for seasonal accumulation of bioactive metals at the base of the McMurdo Sound sea ice by the basal algal community is presented, analogous to a capacitor that accumulates iron during the spring and early summer. The release and transport of particulate metals accumulated at the base of the sea ice by sloughing is discussed as a potentially important mechanism in providing iron nutrition during polynya phytoplankton bloom formation and could be examined in future oceanographic

  10. Dissolved and particulate trace metal micronutrients under the McMurdo Sound seasonal sea ice: basal sea ice communities as a capacitor for iron

    NASA Astrophysics Data System (ADS)

    Noble, Abigail; Saito, Mak; Moran, Dawn; Allen, Andrew

    2013-10-01

    Dissolved and particulate metal concentrations are reported from three sites beneath and at the base of the McMurdo Sound seasonal sea ice in the Ross Sea of Antarctica. This dataset provided insight into Co and Mn biogeochemistry, supporting a previous hypothesis for water column mixing occurring faster than scavenging. Three observations support this: first, Mn-containing particles with Mn/Al ratios in excess of the sediment were present in the water column, implying the presence of bacterial Mn-oxidation processes. Second, dissolved and labile Co were uniform with depth beneath the sea ice after the winter season. Third, dissolved Co:PO43- ratios were consistent with previously observed Ross Sea stoichiometry, implying that over-winter scavenging was slow relative to mixing. Abundant dissolved Fe and Mn were consistent with a winter reserve concept, and particulate Al, Fe, Mn, and Co covaried, implying that these metals behaved similarly. Elevated particulate metals were observed in proximity to the nearby Islands, with particulate Fe/Al ratios similar to that of nearby sediment, consistent with a sediment resuspension source. Dissolved and particulate metals were elevated at the shallowest depths (particularly Fe) with elevated particulate P/Al and Fe/Al ratios in excess of sediments, demonstrating a sea ice biomass source. The sea ice biomass was extremely dense (chl a >9500 μg/L) and contained high abundances of particulate metals with elevated metal/Al ratios. A hypothesis for seasonal accumulation of bioactive metals at the base of the McMurdo Sound sea ice by the basal algal community is presented, analogous to a capacitor that accumulates iron during the spring and early summer. The release and transport of particulate metals accumulated at the base of the sea ice by sloughing is discussed as a potentially important mechanism in providing iron nutrition during polynya phytoplankton bloom formation and could be examined in future oceanographic expeditions.

  11. Influence of land use on total suspended solid and dissolved ion concentrations: Baton Rouge, Louisiana area

    NASA Astrophysics Data System (ADS)

    Carlson, D.

    2015-03-01

    Past studies in the Baton Rouge, Louisiana area considered streamwater quality during storm events but ignored water quality during low flow periods. This study includes determination of streamwater quality during low flow time periods for none watersheds in East Baton Rouge Parish, Louisiana. These samples were collected during dry-low flow periods as indicated by water levels at USGS stream gauging sites for each stream. Chemical analysis for ions was completed using colorimeters and gravimetric analysis for total dissolved solids (TDS) and total suspended solids (TSS). Land use appears to impact concentrations of ions, TDS and TSS in a variety of ways during periods of low flow. The two most rural watersheds, which are mainly underdeveloped, have higher concentrations of Fe and Mn. By contrast the three most urban watersheds, that are mainly commercial, industrial or residential, have higher concentrations of Si, SO4 and TDS.

  12. 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.

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

    SciTech Connect

    Prasetyaningrum, A. Ratnawati,; Jos, B.

    2015-12-29

    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 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.

  14. Statistical evaluation of biogeochemical variables affecting spatiotemporal distributions of multiple free metal ion concentrations in an urban estuary.

    PubMed

    Dong, Zhao; Lewis, Christopher G; Burgess, Robert M; Coull, Brent; Shine, James P

    2016-05-01

    Free metal ion concentrations have been recognized as a better indicator of metal bioavailability in aquatic environments than total dissolved metal concentrations. However, our understanding of the determinants of free ion concentrations, especially in a metal mixture, is limited, due to underexplored techniques for measuring multiple free metal ions simultaneously. In this work, we performed statistical analyses on a large dataset containing repeated measurements of free ion concentrations of Cu, Zn, Pb, Ni, and Cd, the most commonly measured metals in seawater, at five inshore locations in Boston Harbor, previously collected using an in-situ equilibrium-based multi-metal free ion sampler, the 'Gellyfish'. We examined correlations among these five metals by season, and evaluated effects of 10 biogeochemical variables on free ion concentrations over time and location through multivariate regressions. We also explored potential clustering among the five metals through a principal component analysis. We found significant correlations among metals, with varying patterns over season. Our regression results suggest that instead of dissolved metals, pH, salinity, temperature and rainfall were the most significant determinants of free metal ion concentrations. For example, a one-unit decrease in pH was associated with a 2.2 (Cd) to 99 (Cu) times increase in free ion concentrations. This work is among the first to reveal key contributors to spatiotemporal variations in free ion concentrations, and demonstrated the usefulness of the Gellyfish sampler in routine sampling of free ions within metal mixtures and in generating data for statistical analyses. PMID:26901477

  15. 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

  16. Removal of inorganic mercury and methylmercury from surface waters following coagulation of dissolved organic matter with metal-based salts

    USGS Publications Warehouse

    Henneberry, Y.K.; Kraus, T.E.C.; Fleck, J.A.; Krabbenhoft, D.P.; Bachand, P.M.; Horwath, W.R.

    2011-01-01

    The presence of inorganic mercury (IHg) and methylmercury (MeHg) in surface waters is a health concern worldwide. This study assessed the removal potential use of metal-based coagulants as a means to remove both dissolved IHg and MeHg from natural waters and provides information regarding the importance of Hg associations with the dissolved organic matter (DOM) fraction and metal hydroxides. Previous research indicated coagulants were not effective at removing Hg from solution; however these studies used high concentrations of Hg and did not reflect naturally occurring concentrations of Hg. In this study, water collected from an agricultural drain in the Sacramento-San Joaquin Delta was filtered to isolate the dissolved organic matter (DOM) fraction. The DOM was then treated with a range of coagulant doses to determine the efficacy of removing all forms of Hg from solution. Three industrial-grade coagulants were tested: ferric chloride, ferric sulfate, and polyaluminum chloride. Coagulation removed up to 85% of DOM from solution. In the absence of DOM, all three coagulants released IHg into solution, however in the presence of DOM the coagulants removed up to 97% of IHg and 80% of MeHg. Results suggest that the removal of Hg is mediated by DOM-coagulant interactions. There was a preferential association of IHg with the more aromatic, higher molecular weight fraction of DOM but no such relationship was found for MeHg. This study offers new fundamental insights regarding large-scale removal of Hg at environmentally relevant regarding large-scale removal of Hg at environmentally relevant concentrations.

  17. Urinary metal concentrations among female welders.

    PubMed

    Arrandale, Victoria H; Beach, Jeremy; Cembrowski, George S; Cherry, Nicola M

    2015-01-01

    As part of a Canada-wide study of women entering non-traditional trades [Women's Health in Apprenticeship Trades-Metalworkers and Electricians (WHAT-ME)], we examined spot urine samples from women welders in Alberta to determine whether urinary metal concentrations exceeded those of the general population, to compare levels to previously published urinary concentrations in male welders and to examine the relationship with welding tasks. Women mailed-in urine samples collected close to the time of completing a detailed exposure questionnaire, including welding tasks on their most recent day welding at work. Of 53 welders working in their trade, 45 had urinary creatinine >0.3-≤3.0g l(-1) and were included in analyses. Seven metals were examined for which both population and male welder urinary concentrations were available: cadmium, chromium, cobalt, copper, manganese, nickel, and zinc. Principal component analysis was used to extract three components from natural log transformed creatinine-corrected metal concentrations. Of the 45 women, 17 reported more than one main task. Overall two thirds worked in fabrication, a third on pipe welding, and smaller numbers on repair, in construction or other tasks: manual metal arc welding was reported by 62%, semi-automatic arc welding by 47%, and arc welding with a tungsten electrode by 15%. In multiple regression analyses, little relation was found between urinary metals and task or type of welding, except for cadmium where lower levels were seen in those reporting semi-automatic manual welding (after adjustment for age and smoking). The proportion of women welders exceeding the selected general population 95th percentile was high for manganese (96%) and chromium (29%). Urinary metal concentrations were similar to those reported for male welders with only manganese, with a geometric mean in women of 1.91 µg g(-1) creatinine, and perhaps copper (11.8 µg g(-1) creatinine), consistently lower in male welders. Although not

  18. 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...

  19. Concentrations of dissolved herbicides and pharmaceuticals in a small river in Luxembourg.

    PubMed

    Meyer, Berenike; Pailler, Jean-Yannick; Guignard, Cédric; Hoffmann, Lucien; Krein, Andreas

    2011-09-01

    Urban and agricultural areas affect the hydraulic patterns as well as the water quality of receiving drainage systems, especially of catchments smaller than 50 km(2). Urban runoff is prone to contamination due to pollutants like pesticides or pharmaceuticals. Agricultural areas are possible sources of nutrient and herbicide contamination for receiving water bodies. The pollution is derived from leaching by subsurface flow, as well as wash-off and erosion caused by surface runoff. In the Luxembourgish Mess River catchment, the pharmaceutical and pesticide concentrations are comparable with those detected by other authors in different river systems worldwide. Some investigated pesticide concentrations infringe current regulations. The maximum allowable concentration for diuron of 1.8 μg l( - 1) is exceeded fourfold by measured 7.41 μg l( - 1) in a flood event. The load of dissolved pesticides reaching the stream gauge is primarily determined by the amount applied to the surfaces within the catchment area. Storm water runoff from urban areas causes short-lived but high-pollutant concentrations and moderate loads, whereas moderate concentrations and high loads are representative for agricultural inputs to the drainage system. Dissolved herbicides, sulfonamides, tetracyclines, analgesics and hormones can be used as indicators to investigate runoff generation processes, including inputs from anthropogenic sources. The measurements prove that the influence of kinematic wave effects on the relationship between hydrograph and chemographs should not be neglected in smaller basins. The time lag shows that it is not possible to connect analysed substances of defined samples to the corresponding section of the hydrograph. PMID:21110086

  20. Continuous Measurements of the Free Dissolved CO2 Concentration during Photosynthesis of Marine Plants

    PubMed Central

    Brechignac, François; Andre, Marcel

    1985-01-01

    An experimental system consisting of a gas exchange column linked to an assimilation chamber has been developed to record continuously the free dissolved CO2 concentration in seawater containing marine plants. From experiments performed on the red macroalga Chondrus crispus (Rhodophyta, Gigartinales), this measurement is in agreement with the free CO2 concentration calculated from the resistance to CO2 exchanges in a biphasic system (gas and liquid) as earlier reported. The response time of this apparatus is short enough to detect, in conditions of constant pH, a photosynthesis-caused gradient between free CO2 and HCO3− pools which half-equilibrates in 25 seconds. Abolished by carbonic anhydrase, the magnitude of this gradient increases with decreasing time of seawater transit from the chamber to the column apparatus. But its maximum magnitude (0.35 micromolar CO2) is negligible compared to the difference between air and free CO2 (11.4 micromolar CO2). This illustrates the extent of the physical limiting-step occurring at the air-water interface when inorganic carbon consumption in seawater is balanced by dissolving gaseous CO2. The direction of this small free CO2/HCO3− gradient indicates that HCO3− is consumed during photosynthesis. PMID:16664281

  1. Seasonal variations in concentration and lability of dissolved organic carbon in Tokyo Bay

    NASA Astrophysics Data System (ADS)

    Kubo, A.; Yamamoto-Kawai, M.; Kanda, J.

    2015-01-01

    Concentrations of recalcitrant and bioavailable dissolved organic carbon (DOC) and their seasonal variations were investigated at three stations in Tokyo Bay, Japan, and in two freshwater sources flowing into the bay. On average, recalcitrant DOC (RDOC), as a remnant of DOC after 150 days of bottle incubation, accounted for 78% of the total DOC in Shibaura sewage treatment plant (STP) effluent, 67% in the upper Arakawa River water, 66% in the lower Arakawa River water, and 78% in surface bay water. Bioavailable DOC (BDOC) concentrations, defined as DOC minus RDOC, were lower than RDOC at all stations. In freshwater environments, RDOC concentrations were almost constant throughout the year. In the bay, RDOC was higher during spring and summer than in autumn and winter because of freshwater input and biological production. The relative concentration of RDOC in the bay derived from phytoplankton, terrestrial, and open-oceanic waters was estimated to be 8-10, 21-32, and 59-69%, respectively, based on multiple regression analysis of RDOC, salinity, and chl a. In addition, comparison with previous data from 1972 revealed that concentrations of RDOC and BDOC have decreased by 33 and 74% at freshwater sites and 39 and 76% in Tokyo Bay, while the ratio of RDOC to DOC has increased. The change in DOC concentration and composition was probably due to increased amounts of STP effluent entering the system. Tokyo Bay exported mostly RDOC to the open ocean because of the remineralization of BDOC.

  2. Variations in dissolved organic nitrogen concentration in biofilters with different media during drinking water treatment.

    PubMed

    Zhang, Huining; Zhang, Kefeng; Jin, Huixia; Gu, Li; Yu, Xin

    2015-11-01

    Dissolved organic nitrogen (DON) is potential precursor of disinfection byproducts (DBPs), especially nitrogenous DBPs. In this study, we investigated the impact of biofilters on DON concentration 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 concentration first decreased and then increased, and the variation in DON concentration differed among the biofilters. In the activated carbon biofilter, the DON concentration 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 concentration 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 concentration. PMID:25576130

  3. 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

  4. Temporal Variability of Stemflow Dissolved Organic Carbon (DOC) Concentrations and Quality from Morphologically Contrasting Deciduous Canopies

    NASA Astrophysics Data System (ADS)

    van Stan, J. T.; Levia, D. F.; Inamdar, S. P.; Mitchell, M. J.; Mage, S. M.

    2010-12-01

    Dissolved 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 concentrations 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 concentrations 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 concentrations 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 concentration and quality varied with meteorological and antecedent canopy conditions. Since recent studies have linked stemflow production to preferential subsurface transport of dissolved chemistries, trends in DOC speciation and fluxes described in this study may impact soil environments within wooded

  5. 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

  6. [Interpretation of spatial distribution pattern for dissolved inorganic nitrogen concentration in coastal estuary using hyperspectral data].

    PubMed

    Zhang, Dong; Xu, Yong; Zhang, Ying; Li, Huan

    2010-06-01

    Choosing dissolved inorganic nitrogen (DIN) as one of the representative nutritional salt monitoring indexes, a hyperspectral remotely sensed inversion model was built and applied to quantitatively retrieve water quality parameters with its spatial distribution patterns in coastal estuary with high suspended sediment concentration (SSC). It was found that when SSC was larger than 0.1 kg/m3, DIN concentration had a notable inverse correlation with SSC and the correlation coefficient R2 reached 0.617. Based on this conclusion, firstly the in-situ observed water surface remote sensing reflectance was resampled according to the spectral response characters of Hyperion sensor. And then, statistical correlation analysis between reflectance and DIN concentration was carried out. The results showed that band reflectance of R804 and R630 representing the second and first reflectance peak of water spectrum curve were sensitive to the variation of DIN concentration. And then, a pseudo remotely sensed sand parameter index R804 x R630/(R804 - R630) was calculated for the construction of the nonlinear DIN quantitative reversion model. Correlation coefficient R2 between observed and simulated DIN concentrations for 29 calibrating samples and 10 validating samples were 0.746 and 0.67, while their mean absolute errors reached 109.07 and 147.58 microg/L, respectively. The model was then applied on Hyperion hyperspectral image to get the spatial distribution character of DIN concentration in Sheyanghe river estuary and the DIN concentration was between 52 to 513 microg/L. Results indicated that in coastal estuary which was dominated by suspended sediments, the diffusive trends of DIN concentration reversed by remote sensing techniques had an intimate relationship with motions of tidal current and transportation attributes of SSC. As the hydrodynamic conditions were unclear, hyperspectral remote sensing technique was an effective technical way for dynamic survey of DIN concentration

  7. Seasonal variations in concentration and composition of dissolved organic carbon in Tokyo Bay

    NASA Astrophysics Data System (ADS)

    Kubo, A.; Yamamoto-Kawai, M.; Kanda, J.

    2014-07-01

    Concentrations of recalcitrant and bioavailable dissolved organic carbon (DOC) and their seasonal variations were investigated at three stations in Tokyo Bay, Japan, and in two freshwater sources flowing into the bay to evaluate the significance of DOC degradation for the carbon budget in coastal waters and carbon export to the open ocean. Recalcitrant DOC (RDOC) was differentiated from bioavailable DOC (BDOC) as a remnant of DOC after 150 days of bottle incubation. On average, RDOC accounted for 78% of the total DOC in Shibaura sewage treatment plant (STP) effluent, 67% in the upper Arakawa River water, 66% in the lower Arakawa River water, and 78% in surface bay water. RDOC concentrations were higher than BDOC at all stations. In freshwater environments, RDOC concentrations were almost constant throughout the year. In the bay, RDOC was higher during spring and summer than during autumn and winter. The relative abundance of RDOC in the bay derived from phytoplankton, terrestrial, and open oceanic waters was estimated to be 9%, 33%, and 58%, respectively, by multiple regression analysis of RDOC, salinity, and chl a. In addition, comparison with previous data from 1972 revealed that concentrations of RDOC and BDOC have decreased by 33% and 74% at freshwater sites and 39% and 76% at Tokyo Bay, while the ratio of RDOC to DOC has increased. The change in DOC concentration and composition was probably due to increased amounts of sewage treatment plant effluent entering the system. Tokyo Bay exported DOC, mostly RDOC, to the open ocean because of remineralization of BDOC.

  8. Factors Controlling Dissolved Oxygen Concentration in the Hyporheic Zone Induced by Fish Egg Nests

    NASA Astrophysics Data System (ADS)

    Ford, A.; Cardenas, M. B.; Kaufman, M.; Zheng, L.; Kessler, A. J.

    2014-12-01

    There is currently limited research on the effects of bed depressions, such as those associated with fish nests, on hyporheic flow and biogeochemistry. A series of flume experiments are in progress, with the aim of understanding the effects of bed depressions on the hyporheic flow of oxygenated water. This study focuses on fish nests, also called redds, which represent a typical depression or scour feature. Previous research has shown that redd topography induces hyporheic circulation, but experiments regarding the oxygen concentration in and around the redds have not been conducted. We are determining the ways in which redds affect dissolved oxygen distribution and how this is controlled by hyporheic flow. The oxygen concentration across the cross-sectional plane of a fish nest is measured using a planar optode and microsensors. Hydraulic measurements include pressure measurements along the sediment-water interface and dye visualization. The redd design is based on a salmonid redd, which consists of a scour feature and a tailspin. The salmonid eggs are found in the tailspin. We hypothesize that the oxygen concentration will be greatest in close proximity to the gravel base of the redd and concentration will decrease with increasing depth and distance from the redd. Higher oxygen concentrations in the tailspin supports the placement of fish eggs within that area as opposed to a less oxygenated area of the streambed. Thus, fish nests are likely bio-engineered to optimize hyporheic flow and biogeochemistry to improve egg viability.

  9. 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.

  10. Long term in situ monitoring of total dissolved iron concentrations on the MoMAR observatory

    NASA Astrophysics Data System (ADS)

    Laes-Huon, Agathe; Legrand, Julien; Tanguy, Virginie; Cathalot, Cecile; Blandin, Jérôme; Rolin, Jean-Francois; Sarradin, Pierre-Marie

    2015-04-01

    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 dissolved iron concentrations associated with an optode and a temperature probe. Several months of total iron concentrations, 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 dissolved 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 dissolved iron concentrations 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

  11. Regulation of the dissolved phosphate concentration of a mountainous stream, Kitakyushu, southwestern Japan.

    PubMed

    Koga, Masaaki; Yoshimura, Kazuhisa

    2012-07-01

    The phosphate concentration in mountainous stream water can be a measure of the forest condition, because its concentration 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 dissolved phosphate concentration of the mountainous stream water of the Yamakami River, Kitakyushu, from June 2009 to August 2010, and the regulation mechanism of the phosphate concentration, 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 concentrations 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 concentration were fairly small even during a storm runoff. The average phosphate concentration of rain was 2.8 ± 0.7 μg P L(-1), about half of the concentration 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 concentration 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 concentration was the highest, suggesting that the biomass may still be decreasing. For all of the six sites examined, a characteristic seasonal change in phosphate concentration was observed, reflecting the local budget between the biological decomposition of plant matter and the consumption by the biomass. The increase in the phosphate concentration 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

  12. Metal concentrations in soil paste extracts as affected by extraction ratio.

    PubMed

    Tack, Filip M G; Dezillie, Nic; Verloo, Marc G

    2002-04-01

    Saturated paste extracts are sometimes used to estimate metal levels in the soil solution. To assess the significance of heavy-metal concentrations measured in saturation extracts, soil paste extracts were prepared with distilled water in amounts ranging from 60-200% of the moisture content at saturation. Trace metals behaved as if a small pool consistently was dissolved independent of the extraction ratio applied. Metal concentrations in the solution hence were not buffered by the solid phase, but the observed behaviour would allow the estimation of metal concentrations in the soil solution as a function of moisture content. The behaviour of iron and manganese suggested that some microbial reduction occurred. The intensity increased with increasing extraction ratio but not to the extent of affecting dissolution of trace elements. PMID:12805950

  13. Quantifying dissolved organic carbon concentrations in upland catchments using phenolic proxy measurements

    NASA Astrophysics Data System (ADS)

    Peacock, Mike; Burden, Annette; Cooper, Mark; Dunn, Christian; Evans, Chris D.; Fenner, Nathalie; Freeman, Chris; Gough, Rachel; Hughes, David; Hughes, Steve; Jones, Tim; Lebron, Inma; West, Mike; Zieliński, Piotr

    2013-01-01

    SummaryConcentrations of dissolved organic carbon (DOC) in soil and stream waters in upland catchments are widely monitored, in part due to the potential of DOC to form harmful by-products when chlorinated during treatment of water for public supply. DOC can be measured directly, though this is expensive and time-consuming. Light absorbance in the UV-vis spectrum is often used as a surrogate measurement from which a colour-carbon relationship between absorbance and DOC can be derived, but this relationship can be confounded by numerous variables. Through the analysis of data from eight sites in England and Wales we investigate the possibility of using the concentration of phenolic compounds in water samples as a proxy for DOC concentration. A general model using data from all the sites allowed DOC to be calculated from phenolics at an accuracy of 81-86%. A detailed analysis at one site revealed that a site-specific calibration was more accurate than the general model, and that this compared favourably with a colour-carbon calibration. We therefore recommend this method for use where estimates of DOC concentration are needed, but where time and money are limiting factors, or as an additional method to calculate DOC alongside colour-carbon calibrations. Tests demonstrated only small amounts of phenolic degradation over time; a loss of 0.92 mg L-1 after 8 months in storage, and so this method can be used on older samples with limited loss of accuracy.

  14. Raising and controlling study of dissolved oxygen concentration in closed-type aeration tank.

    PubMed

    Chen, C K; Lo, S L

    2005-07-01

    This study investigated the promotion and control of dissolved oxygen (DO) concentration of the closed-type aeration tank via practical experiments in the wastewater treatment system of a 5-star hotel in Taipei. As with limited and treasured space in Taiwan, before the completion of the sewer system construction in cities, to utilize the mat foundation under large buildings as the space of sewage treatment plant still has been one of the alternatives of those sewage treatments. However, aeration tanks constructed in the mat foundation of buildings have smaller effective water depth, which will cause a lower total transfer amount of DO. Controlling the total exhaust gas flow rate can increase the pressure on such closed-type aeration tanks. The DO concentration thus may increase according to Henry's Law. Furthermore, it may enable operators to adjust the DO concentration of the aeration tank more precisely and thus sustain optimal operating conditions in these treatment facilities. Practical experiments indicated that the DO concentration of aeration tank maintains an average of 3.8 mg l(-1), obtaining the optimum operating conditions. The efficiency of the biological treatment facilities in the mat foundation could be markedly improved. PMID:16080335

  15. Collective excitations in concentric metallic nanoshells

    NASA Astrophysics Data System (ADS)

    Bose, Shyamalendu; Zale, Edward

    2006-03-01

    Invention of nanoshells made of a silica core coated with an ultra-thin metallic layer [1] has opened a floodgate of many applications in medical and other fields. Most of these applications are triggered by the fact that the nanoshells have unusual electronic and optical properties which can be controlled by controlling the inner and outer radii of the nanoshell. Employing a classical hydrodynamic model, we have obtained a general expression for the resonant frequencies (plasmons) of the electrons for N concentric nanoshells. Results obtained using this theory will be compared with previous calculations for two concentric nanoshells [2] and possible applications of the new results will be discussed. 1. S.J. Oldenburg, et al., Chem. Phys. Letts. 288, 243 (1998). 2. E. Prodan, et al.., Science 302, 419 (2003).

  16. Evaluation of Electrodialysis as Part of an Improved Method to Concentrate Dissolved Organic Matter from Seawater

    NASA Astrophysics Data System (ADS)

    Chang, V.; Koprivnjak, J.; Ingall, E.; Pfromm, P.; Perdue, E. M.

    2004-12-01

    A major obstacle in the study of marine dissolved organic matter (DOM) has been isolating from seawater sufficient quantities for analysis of this highly dilute and chemically complex material. This research explores the application of electrodialysis (ED) in combination with reverse osmosis (RO) as a method to concentrate DOM from seawater. RO methods recover a significant fraction (90%) of DOM from fresh waters with little physical or chemical alteration, and similar high recoveries of DOM have been observed in preliminary tests using estuarine waters of varying salinity. Unfortunately, the extent to which DOM in saline waters can be concentrated by RO is very limited, because RO membranes co-concentrate inorganic salts with DOM. At an early stage of processing, osmotic pressures become too high and/or inorganic salts precipitate from solution and foul the RO membrane. To realize the potentially high recoveries of DOM from saline waters, RO must be coupled with an independent method for removal of inorganic salts. Electrodialysis, which is a well-established process for removal of inorganic salts from aqueous solutions, is such a method. In ED, a feed stream of the sample to be de-ionized and a receiving stream of a solution that will accept the removed ions are pumped through adjacent layers of a membrane stack, which consists of several layers of alternating anion and cation exchange membranes. The membranes are made from highly crosslinked polymers and are non-porous. The direction and velocity of diffusion of the cations and anions are further mediated by a DC electrical current that flows through the membrane stack. In the first stage of testing of the ED process, samples of near-seawater salinity (28 ppt) containing 4 ppm of dissolved organic carbon were collected at the Skidaway Institute of Oceanography in Savannah Georgia. Using ED, salinity was reduced by 87% in these samples with retention of more than 95% of the DOM. These experiments indicate that ED

  17. Effect of iron bioavailability on dissolved hydrogen concentrations during microbial iron reduction.

    PubMed

    Komlos, John; Jaffé, Peter R

    2004-10-01

    Dissolved hydrogen (H2) concentrations have been shown to correlate with specific terminal electron accepting processes (TEAPs) in aquifers. The research presented herein examined the effect of iron bioavailability on H2 concentrations during iron reduction in flow-through column experiments filled with soil obtained from the uncontaminated background area of the Field Research Center (FRC), Oak Ridge, TN and amended with acetate as the electron donor. The first column experiment measured H2 concentrations over 500 days of column operation that fluctuated within a substantial range around an average of 3.9 nM. Iron reduction was determined to be the dominant electron accepting process. AQDS (9,10-anthraquinone-2,6-disulfonic acid) was then used to determine if H2 concentrations during iron reduction were related to iron bioavailability. For this purpose, a 100-day flow-through column experiment was conducted that compared the effect of AQDS on iron reduction and subsequent H2 concentrations using two columns in parallel. Both columns were packed with FRC soil and inoculated with Geobacter sulfurreducens but only one was supplied with AQDS. The addition of AQDS increased the rate of iron reduction in the flow-through column and slightly decreased the steady-state H2 concentrations from an average of 4.0 nM for the column without AQDS to 2.0 nM for the column with AQDS. The results of this study therefore show that H2 can be used as an indicator to monitor rate and bioavailability changes during microbial iron reduction. PMID:15523914

  18. Temporal and spatial variations in dissolved trace metal species in the Chesapeake Bay

    NASA Astrophysics Data System (ADS)

    Sako, A.; Hannigan, R.; Jones, C.

    2002-12-01

    Behavior of dissolved major (e.g., Mg2+, Ca2+ and K+) and trace elements (e.g., Sr2+, Pb2+, Ba2+, Br-, etc.) in estuarine environments is a function of several factors such as salinity, pH, suspended particles and organic material contents. The fate of these metals and their distribution will differ from one estuary to another and within a given estuary. To investigate the fate and source (anthropogenic versus resuspended input) of selected major and trace elements in Chesapeake Bay (CB), water and sediment samples were collected eastern, western shores and island areas of the Bay from July to September. Water samples were filtered (0.45\\x8Dm) and acidified (pH<2) with ultrapure nitric acid prior to their analysis for trace elements by ICP-MS. A computer code (MINTEQA) was used to study metal speciation in water samples. It was assumed that water was in equilibrium with atmospheric oxygen, and therefore Fe3+ form was input in the model instead of Fe2+. As a result, MINTEQA did not have to perform redox calculations. The ratio of dissolved species to total dissolved metal indicates nonconservative behavior of major elements such Mg, Ca and K and Pb, while trace elements Sr and Ba were more conservative, in time and space. Variations in ionic strengths in different sites suggest effects of salinity and turbidity on complex formation, as ionic strength normally increases with low salinity and vice versa. Variations in spatial and temporal distribution of elements, shown in this study, are likely due to nonuniformity of the water flow regime in different zones, seasonal biological regeneration of metals from sediment and salinity gradients.

  19. Specific conductance and dissolved chloride concentrations of freshwater aquifers and streams in petroleum producing areas in Mississippi

    USGS Publications Warehouse

    Kalkhoff, S.J.

    1982-01-01

    Specific conductance and dissolved chloride reconnasissance sampling was conducted in six oil-producing areas of Mississippi during periods of low streamflow in 1980 and 1981. Water samples were collected at 224 ground-water and 190 suface-water sites. Samples from 55 surface-water and 17 ground-water sites contained dissolved chloride concentrations in excess of 100 milligrams per liter. All data collected are presented in tables without interpretation. (USGS)

  20. Diminished Stream Nitrate Concentrations Linked to Dissolved Organic Carbon Dynamics After Leaf Fall

    NASA Astrophysics Data System (ADS)

    Sebestyen, S. D.; Shanley, J. B.; Boyer, E. W.; Doctor, D. H.; Kendall, C.

    2004-05-01

    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 dissolved 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 concentration patterns were quantitatively different from other times of the year. Under baseflow conditions, stream and soil water DOC concentrations were higher than normal, whereas nitrate concentrations 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.

  1. Acquiring reproducible fluorescence spectra of dissolved organic matter at very low concentrations.

    PubMed

    Peiris, B R H; Budman, H; Moresoli, C; Legge, R L

    2009-01-01

    A method that would allow for fast and reliable measurements of dissolved organic matter (DOM), both at low and high concentration levels would be a valuable tool for online monitoring of DOM. This could have applications in a variety of areas including membrane treatment systems for drinking water applications which is of interest to our group. In this study, the feasibility of using fluorescence spectroscopy for monitoring DOM at very low concentration levels was demonstrated with an emphasis on optimizing the instrument parameters necessary to obtain reproducible fluorescence signals. Signals were acquired using a cuvette or a fibre optic probe assembly, the latter which may have applications for on-line or in-line monitoring. The instrument parameters such as photomultiplier tube (PMT) voltage, scanning rate and slit width were studied in detail to find the optimum parameter settings required. The results showed that larger excitation and emission slit widths were preferred, over larger PMT voltage or lower scanning rates, to obtain reproducible and rapid measurements when measuring very low concentration levels of DOM. However, this approach should be implemented with caution to avoid any reduction of the signal resolution. PMID:19759440

  2. Glucose fluxes and concentrations of dissolved combined neutral sugars (polysaccharides) in the Ross Sea and Polar Front Zone, Antarctica

    NASA Astrophysics Data System (ADS)

    Kirchman, David L.; Meon, Benedikt; Ducklow, Hugh W.; Carlson, Craig A.; Hansell, Dennis A.; Steward, Grieg F.

    We hypothesized that dissolved carbohydrates would be large components of the labile dissolved organic carbon (DOC) pool and would support much bacterial growth in Antarctic waters, especially the Ross Sea, since previous work had observed extensive phytoplankton blooms with potentially high production rates of carbohydrates in Antarctic seas. These hypotheses were tested on cruises in the Ross Sea and Antarctic Polar Front Zone as part of the US JGOFS program. Concentrations and fluxes of free glucose (the only free sugar detected) were very low, but dissolved polysaccharides appeared to be important components of the DOC pool. Concentrations of dissolved combined neutral sugars increased >3-fold during the phytoplankton bloom in the Ross Sea and were a large fraction (ca. 50%) of the semi-labile fraction of DOC. The relatively high concentrations of dissolved combined neutral sugars, which are thought to be quite labile, appear to explain why DOC accumulated during the phytoplankton bloom was degraded so quickly once the bloom ended. Some of the polysaccharides appeared to be more refractory, however, since dissolved combined neutral sugars were observed in deep waters (>550 m) and in early spring (October) in the Ross Sea, apparently having survived degradation for >8 months. The molecular composition of these refractory polysaccharides differed from that of polysaccharides sampled during the phytoplankton bloom. Fluxes of DOC were low in the Ross Sea compared to standing stocks and fluxes of particulate material, but the DOC that did accumulate during the phytoplankton bloom appeared to be sugar-rich and relatively labile.

  3. Dissolved Organic Matter Characteristics Control Filtered Total Mercury Concentrations in an Adirondack River Basin

    NASA Astrophysics Data System (ADS)

    Burns, D. A.; Aiken, G.; Bradley, P. M.; Journey, C.

    2011-12-01

    Dissolved organic carbon (DOC) plays important roles in the transport and biogeochemical processes that affect mercury (Hg) cycling in the environment. Previous investigations have shown strong correlations between DOC and Hg concentrations in surface waters. Commonly, other DOC-related measures such as ultraviolet absorbance (UV254), and hydrophobic acid content (HPOA) show even stronger positive correlations with Hg in waters indicating the importance of the more aromatic fraction of DOC in Hg cycling. Finally, in-situ optical sensor-derived DOC concentrations have proven useful as inexpensive proxies for estimating Hg concentrations in some surface waters. Here, we describe results from the 493 km2 Upper Hudson River basin in the Adirondack Mountains of New York in which stream water samples were collected for filtered total Hg (FTHg) concentrations, DOC concentrations, UV254, HPOA, and specific ultraviolet absorbance (SUVA, derived from the absorbance and DOC measurements) at two temporal and spatial scales during 2006-09: (1) biweekly to monthly in a 66 km2 basin, and (2) seasonally at 27 synoptic sites distributed across the larger Upper Hudson basin. These results indicate that SUVA values are more strongly correlated with FTHg concentrations than are those of DOC concentrations, especially during summer. The presence of numerous open water bodies in this basin appears to greatly affect DOC and FTHg concentrations and SUVA values as reflected by data collected upstream and downstream of ponds and lakes. Multivariate regression models developed to examine the landscape factors that control spatial variation in SUVA values among synoptic sites indicate that open water area is inversely correlated with these values, reflecting autochthonous carbon sources in lakes/ponds that are more aliphatic in character than that found in streams. In contrast, metrics such as percent riparian area that reflect the influence of soils with high organic carbon content are

  4. Fractionation and size-distribution of metal and metalloid contaminants in a polluted groundwater rich in dissolved organic matter.

    PubMed

    Kozyatnyk, Ivan; Bouchet, Sylvain; Björn, Erik; Haglund, Peter

    2016-11-15

    We investigated the concentration levels, fractionation and molecular weight distribution (MWD) of dissolved organic matter (DOM) and metals (V, Cr, Co, Ni, Cu, Zn, As, Cd, Sn, Ba, Hg and Pb) in a polluted groundwater from an industrial area in Northern Sweden. DOM was mainly recovered in the hydrophobic acidic and hydrophobic neutral sub-fractions (45 and 35%, respectively) while most metals were found in the acidic sub-fractions (46-93%) except for V, Fe and As, which were predominant in the basic sub-fractions (74-93%) and Cd in the neutral ones (50%). DOM exhibited a broad MWD in groundwaters, usually from 5 to 200kDa and was dominated by high molecular weight hydrophobic acids, low molecular weight hydrophilic acids and hydrophilic neutral compounds. Most of the studied metals (Fe, Cr, Co, Sn, Ba, Hg) were associated with the high molecular weight DOM fraction (ca. 40-100kDa). Cu, Pb, Zn, Cd and Ni interacted with a broad range of DOM size fractions but were still most abundant in the high molecular weight fraction. Few metal/metalloids (As, V and Cr in some cases) presented a very weak affinity for DOM and presumably existed predominantly as "free" inorganic ions in solution. PMID:27427886

  5. Salicylhydroxamic acid (SHAM) inhibition of the dissolved inorganic carbon concentrating process in unicellular green algae

    SciTech Connect

    Goyal, A.; Tolbert, N.E. )

    1990-03-01

    Rates of photosynthetic O{sub 2} evolution, for measuring K{sub 0.5}(CO{sub 2} + HCO{sub 3}{sup {minus}}) at pH 7, upon addition of 50 micromolar HCO{sub 3}{sup {minus}} to air-adapted Chlamydomonas, Dunaliella, or Scenedesmus cells, were inhibited up to 90% by the addition of 1.5 to 4.0 millimolar salicylhydroxamic acid (SHAM) to the aqueous medium. The apparent K{sub i}(SHAM) for Chlamydomonas cells was about 2.5 millimolar, but due to low solubility in water effective concentrations would be lower. Salicylhydroxamic acid did not inhibit oxygen evolution or accumulation of bicarbonate by Scenedesmus cells between pH 8 to 11 or by isolated intact chloroplasts from Dunaliella. Thus, salicylhydroxamic acid appears to inhibit CO{sub 2} uptake, whereas previous results indicate that vanadate inhibits bicarbonate uptake. These conclusions were confirmed by three test procedures with three air-adapted algae at pH 7. Salicylhydroxamic acid inhibited the cellular accumulation of dissolved inorganic carbon, the rate of photosynthetic O{sub 2} evolution dependent on low levels of dissolved inorganic carbon (50 micromolar NaHCO{sub 3}), and the rate of {sup 14}CO{sub 2} fixation with 100 micromolar ({sup 14}C)HCO{sub 3}{sup {minus}}. Salicylhydroxamic acid inhibition of O{sub 2} evolution and {sup 14}CO{sub 2}-fixation was reversed by higher levels of NaHCO{sub 3}. Thus, salicylhydroxamic acid inhibition was apparently not affecting steps of photosynthesis other than CO{sub 2} accumulation. Although salicylhydroxamic acid is an inhibitor of alternative respiration in algae, it is not known whether the two processes are related.

  6. Effects of fluoride and dissolved oxygen concentrations on the corrosion behavior of pure titanium and titanium alloys.

    PubMed

    Nakagawa, Masaharu; Matsuya, Shigeki; Udoh, Koichi

    2002-06-01

    The effects of dissolved-oxygen concentration and fluoride concentration on the corrosion behaviors of commercial pure titanium, Ti-6Al-4V and Ti-6Al-7Nb alloys and experimentally produced Ti-0.2Pd and Ti-0.5Pt alloys were examined using the corrosion potential measurements. The amount of dissolved Ti was analyzed by inductively coupled plasma mass spectroscopy. A decrease in the dissolved-oxygen concentration tended to reduce the corrosion resistance of Ti and Ti alloys. If there was no fluoride, however, corrosion did not occur. Under low dissolved-oxygen conditions, the corrosion of pure Ti and Ti-6Al-4V and Ti-6Al-7Nb alloys might easily take place in the presence of small amounts of fluoride. They were corroded by half or less of the fluoride concentrations in commercial dentifrices. The Ti-0.2Pd and Ti-0.5Pt alloys did not corrode more, even under the low dissolved-oxygen conditions and a fluoride-containing environment, than pure Ti and Ti-6Al-4V and Ti-6Al-7Nb alloys. These alloys are expected to be useful as new Ti alloys with high corrosion resistance in dental use. PMID:12238790

  7. Novel method for online monitoring of dissolved N2O concentrations through a gas stripping device.

    PubMed

    Mampaey, Kris E; van Dongen, Udo G J M; van Loosdrecht, Mark C M; Volcke, Eveline I P

    2015-01-01

    Nitrous oxide emissions from wastewater treatment plants are currently measured by online gas phase analysis or grab sampling from the liquid phase. In this study, a novel method is presented to monitor the liquid phase N2O concentration for aerated as well as non-aerated conditions/reactors, following variations both in time and in space. The monitoring method consists of a gas stripping device, of which the measurement principle is based on a continuous flow of reactor liquid through a stripping flask and subsequent analysis of the N2O concentration in the stripped gas phase. The method was theoretically and experimentally evaluated for its fit for use in the wastewater treatment context. Besides, the influence of design and operating variables on the performance of the gas stripping device was addressed. This method can easily be integrated with online off-gas measurements and allows to better investigate the origin of the gas emissions from the treatment plant. Liquid phase measurements of N2O are of use in mitigation of these emissions. The method can also be applied to measure other dissolved gasses, such as methane, being another important greenhouse gas. PMID:25573615

  8. Concentration, sources and flux of dissolved organic carbon of precipitation at Lhasa city, the Tibetan Plateau

    NASA Astrophysics Data System (ADS)

    Li, C.

    2015-12-01

    Dissolved organic carbon (DOC) plays important role in 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 concentration and wet deposition fluxes of DOC was 1.10 mg C/L and 0.62 g C m-2.yr-1, respectively. Seasonally, low DOC concentration and high flux appeared during 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 cites (e.g. Beijing and Seoul) mainly because of less air pollution of Lhasa. The relationship between DOC and ion analysis showed that DOC of Lhasa was derived mainly from the natural sources, followed by burning activities. Furthermore, △14C value of DOC indicated that fossil combustion contributed around 20% of the precipitation DOC of Lhasa, indicating that the atmosphere of Lhasa has been influenced by vehicle emissions. Therefore, although atmosphere of Lhasa is relatively clean, pollutants emitted from local sources cannot be ignored.

  9. Concentration, sources, and flux of dissolved organic carbon of precipitation at Lhasa city, the Tibetan Plateau.

    PubMed

    Li, Chaoliu; Yan, Fangping; Kang, Shichang; Chen, Pengfei; Qu, Bin; Hu, Zhaofu; Sillanpää, Mika

    2016-07-01

    Dissolved 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 concentration 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 concentration 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. PMID:26988365

  10. Influence of groundwater recharge and well characteristics on dissolved arsenic concentrations in southeastern Michigan groundwater

    USGS Publications Warehouse

    Meliker, J.R.; Slotnick, M.J.; Avruskin, G.A.; Haack, S.K.; Nriagu, J.O.

    2009-01-01

    Arsenic concentrations 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 dissolved arsenic concentrations, 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.

  11. Dissolved oxygen concentration in the medium during cell culture: Defects and improvements.

    PubMed

    Zhang, Kuan; Zhao, Tong; Huang, Xin; He, Yunlin; Zhou, Yanzhao; Wu, Liying; Wu, Kuiwu; Fan, Ming; Zhu, Lingling

    2016-03-01

    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 concentrations in the medium are much greater in 25-cm(2) flasks than in 24-well plates and 35-mm dishes. The dissolved oxygen concentrations 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. PMID:26648388

  12. Foam-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    DOEpatents

    Janke, Christopher J.; Dai, Sheng; Oyola, Yatsandra

    2015-06-02

    Foam-based adsorbents and a related method of manufacture are provided. The foam-based adsorbents include polymer foam with grafted side chains and an increased surface area per unit weight to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. A method for forming the foam-based adsorbents includes irradiating polymer foam, grafting with polymerizable reactive monomers, reacting with hydroxylamine, and conditioning with an alkaline solution. Foam-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  13. Powder-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    DOEpatents

    Janke, Christopher J.; Dai, Sheng; Oyola, Yatsandra

    2016-05-03

    A powder-based adsorbent and a related method of manufacture are provided. The powder-based adsorbent includes polymer powder with grafted side chains and an increased surface area per unit weight to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. A method for forming the powder-based adsorbent includes irradiating polymer powder, grafting with polymerizable reactive monomers, reacting with hydroxylamine, and conditioning with an alkaline solution. Powder-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  14. 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. PMID:26596969

  15. Dissolved methane concentration profiles and air-sea fluxes from 41°S to 27°N

    NASA Astrophysics Data System (ADS)

    Kelley, Cheryl A.; Jeffrey, Wade H.

    2002-07-01

    Water column samples from a transect cruise from southern Chile through the Panama Canal to the Gulf of Mexico were used to determine dissolved methane depth profiles and air-sea methane fluxes. In the Gulf of Mexico, surface concentrations were approximately 40% supersaturated with respect to the atmosphere, whereas near the equator and in the Peru upwelling region, 10-20% supersaturation generally occurred. These saturation ratios translate into an average flux of methane from the sea surface to the atmosphere of 0.38 μmol m-2 d-1. In addition, water column profiles of dissolved methane indicate that subsurface maxima in dissolved methane concentrations are a consistent feature of the open ocean, except near the equator. At the equator, the subsurface peak at the base of the mixed layer may be bowed down by the Equatorial Undercurrent. The highest methane concentration (12 nM) was observed in the Peru upwelling region.

  16. Response of dissolved carbon and nitrogen concentrations to moderate nutrient additions in a tropical montane forest of south Ecuador

    NASA Astrophysics Data System (ADS)

    Velescu, Andre; Valarezo, Carlos; Wilcke, Wolfgang

    2016-05-01

    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 dissolved 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 concentrations in throughfall increased following N+P additions, while separate N amendments only increased nitrate concentrations. Total organic carbon (TOC) and dissolved organic nitrogen (DON) concentrations 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

  17. Changes in glucose fermentation pathways by an enriched bacterial culture in response to regulated dissolved H2 concentrations.

    PubMed

    Zheng, Hang; Zeng, Raymond J; Duke, Mikel C; O'Sullivan, Cathryn A; Clarke, William P

    2015-06-01

    It is well established that metabolic pathways in the fermentation of organic waste are primarily controlled by dissolved H2 concentrations, but there is no reported study that compares observed and predicted shifts in fermentation pathways induced by manipulating the dissolved H2 concentration. A perfusion system is presented that was developed to control dissolved H2 concentrations in the continuous fermentation of glucose by a culture highly enriched towards Thermoanaerobacterium thermosaccharolyticum (86 ± 9% relative abundance) from an originally diverse consortia in the leachate of a laboratory digester fed with municipal solid waste. Media from a 2.5 L CSTR was drawn through sintered steel membrane filters to retain biomass, allowing vigorous sparging in a separate chamber without cellular disruption. Through a combination of sparging and variations in glucose feeding rate from 0.8 to 0.2 g/L/d, a range of steady state fermentations were performed with dissolved H2 concentrations as low as an equivalent equilibrated H2 partial pressure of 3 kPa. Trends in product formation rates were simulated using a H2 regulation partitioning model. The model correctly predicted the direction of products redistribution in response to H2 concentration changes and the acetate and butyrate formation rates when H2 concentrations were less than 6 kPa. However, the model over-estimated acetate, ethanol and butanol productions at the expense of butyrate production at higher H2 concentrations. The H2 yield at the lowest dissolved H2 concentration was 2.67 ± 0.08 mol H2 /mol glucose, over 300% higher than the yield achieved in a CSTR operated without sparging. PMID:25545692

  18. Influence of Dissolved Metals on N-Nitrosamine Formation under Amine-based CO2 Capture Conditions.

    PubMed

    Wang, Zimeng; Mitch, William A

    2015-10-01

    As the prime contender for postcombustion CO2 capture technology, amine-based scrubbing has to address the concerns over the formation of potentially carcinogenic N-nitrosamine byproducts from reactions between flue gas NOx and amine solvents. This bench-scale study evaluated the influence of dissolved metals on the potential to form total N-nitrosamines in the solvent within the absorber unit and upon a pressure-cooker treatment that mimics desorber conditions. Among six transition metals tested for the benchmark solvent monoethanolamine (MEA), dissolved Cu promoted total N-nitrosamine formation in the absorber unit at concentrations permitted in drinking water, but not the desorber unit. The Cu effect increased with oxygen concentration. Variation of the amine structural characteristics (amine order, steric hindrance, -OH group substitution and alkyl chain length) indicated that Cu promotes N-nitrosamine formation from primary amines with hydroxyl or carboxyl groups (amino acids), but not from secondary amines, tertiary amines, sterically hindered primary amines, or amines without oxygenated groups. Ethylenediaminetetraacetate (EDTA) suppressed the Cu effect. The results suggested that the catalytic effect of Cu may be associated with the oxidative degradation of primary amines in the absorber unit, a process known to produce a wide spectrum of secondary amine products that are more readily nitrosatable than the pristine primary amines, and that can form stable N-nitrosamines. This study highlighted an intriguing linkage between amine degradation (operational cost) and N-nitrosamine formation (health hazards), all of which are challenges for commercial-scale CO2 capture technology. PMID:26335609

  19. Concentration studies of collision-induced fundamental absorption of hydrogen dissolved in liquid neon.

    PubMed

    Herrebout, W A; van der Veken, B J; Kouzov, A P

    2012-08-28

    We report further and more detailed results of our recent investigation [W. A. Herrebout, B. J. van der Veken, and A. P. Kouzov, Phys. Rev. Lett. 101, 093001 (2008)] on the collision-induced fundamental absorption by hydrogen dissolved in liquid neon (T ≈ 25 K). The band shapes were studied in a wide range of concentrations (0.003-0.05 mole fractions) as well as for different ortho/para ratios and at much higher level of accuracy and resolution than before. Due to almost unhindered rotation of the hydrogen molecule and low temperature, an unprecedently rich frequency-domain picture produced by different terms of the interaction-induced polarization was observed. While some of them are conspicuous via fast intracell motion of a light guest (H(2)), others--induced by the electrostatic field of the guest--give rise to lines whose shapes are imprinted by fluctuations of the nearest surrounding. Strong motional narrowing observed on the guest-guest induced lines shows up in their Lorentzian shapes which are signatures of microscopic-scale diffusion. Near-Lorentzian peaks were also detected at the tops of the diffuse lines induced by isolated guests. Their formation may be associated with a long-living defect (vacancy) emerging in the vicinity of the polarization inductor. Altogether, our results give the first unambiguous spectroscopic evidence on the diffusional evolution of isolated binary interactions that emerge in dense chaotic media. PMID:22938252

  20. Direct measurement of local dissolved oxygen concentration spatial profiles in a cell culture environment.

    PubMed

    Kagawa, Yuki; Matsuura, Katsuhisa; Shimizu, Tatsuya; Tsuneda, Satoshi

    2015-06-01

    Controlling local dissolved oxygen concentration (DO) in media is critical for cell or tissue cultures. Various biomaterials and culture methods have been developed to modulate DO. Direct measurement of local DO in cultures has not been validated as a method to test DO modulation. In the present study we developed a DO measurement system equipped with a Clark-type oxygen microelectrode manipulated with 1 μm precision in three-dimensional space to explore potential applications for tissue engineering. By determining the microelectrode tip position precisely against the bottom plane of culture dishes with rat or human cardiac cells in static monolayer culture, we successfully obtained spatial distributions of DO in the medium. Theoretical quantitative predictions fit the obtained data well. Based on analyses of the variance between samples, we found the data reflected "local" oxygen consumption in the vicinity of the microelectrode and the detection of temporal changes in oxygen consumption rates of cultured cells was limited by the diffusion rate of oxygen in the medium. This oxygen measuring system monitors local oxygen consumption and production with high spatial resolution, and can potentially be used with recently developed oxygen modulating biomaterials to design microenvironments and non-invasively monitor local DO dynamics during culture. PMID:25565074

  1. Heavy metal behavior and dissolved organic matter (DOM) characterization of vermicomposted pig manure amended with rice straw.

    PubMed

    Zhu, Weiqin; Yao, Wu; Zhang, Zhi; Wu, Yang

    2014-11-01

    Vermicomposting is an eco-friendly method for disposing of livestock and poultry manure. In addition, dissolved organic matter (DOM) can serve as a carrier that enhances the migration and transformation of heavy metals. Here, pig manure amended with rice straw was vermicomposted with Eisenia fetida. The DOM content, molecular weight distribution, and spectroscopic properties of the amended pig manure were measured before and after vermicomposting. The Cu and Zn concentrations in the earthworms increased from 8.24 and 17.63 to 40.75 and 362.78 mg/kg separately after vermicomposting, and the earthworms also increased the heavy metal availability in the vermicompost. Relative to the DOM properties of conventional compost, the DOM molecular weight decreased and varied widely following vermicomposting, and the C/N ratio of the DOM in the vermicompost treatments decreased from 10.37 to 8.60. The Fourier transform far-infrared (FTIR) and fluorescence spectra of the DOM indicated that the amounts of oxygen-containing structures increased while the ratio of humic acid to fulvic acid decreased following vermicomposting. Accordingly, the earthworms augmented the heavy metal mitigation risk in the pig manure. This augment potentially resulted from the decreased humic acid-to-fulvic acid (HA/FA) ratio from DOM structural changes. PMID:24958537

  2. Hydrologically Driven Dynamics of Dissolved Organic Carbon Concentration and Composition in a Headwater Stream Ecosystem

    NASA Astrophysics Data System (ADS)

    Kaplan, L. A.; McLaughlin, C.; Hogan, K. R.; Newbold, J. D.

    2011-12-01

    A 34-year record of dissolved organic carbon (DOC) concentrations and compositions was used to assess the role of hydrologic variability in the carbon cycle of a headwater stream. The DOC concentration record is characterized by sharply increasing values during storms and annual minima associated with soil freezing in winter (Fig. 1). Baseflow discharge accounts for approximately 67% of the total runoff in this 3rd-order stream in the Pennsylvania Piedmont but storm flows transport approximately 75% of the DOC flux. The annual DOC flux varies as much as 3-fold and this variability is driven by unusual events such as major storms and prolonged droughts. During storms DOC quality changes as water moves to the stream through organic matter-rich upper soil horizons, by passing terrestrial controls on DOC content. The pool of biodegradable DOC (BDOC) as a percentage of total DOC increases from 33% to 73% with the most labile BDOC class increasing 4-fold while the semi-labile BDOC pool increases 2-fold. Storms also alter the structure and productivity of benthic bacterial communities that metabolize DOC in streams, though the impacts are tempered by stability of streambed substrata. For example, a February storm reduced the biomass and productivity of bacteria attached to sediments by 48% and 90%, respectively, while reducing the biomass of bacteria attached to rocks by 21% but increasing bacterial productivity by 22%. Molecular fingerprints of community compositions revealed a stable "climax community" whose alteration is influenced by the magnitude of the storm flows and eventually returns to its original composition. Actual measurements of carbon cycling based on whole-stream releases and sampling the stream bed microbial community are not feasible during storms, but we argue that for headwater streams it is the post-disturbance condition rather than any processing which occurs during storm flows that shapes the magnitude and dynamics of carbon cycling.

  3. 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

  4. Geochemistry of dissolved trace elements and heavy metals in the Dan River Drainage (China): distribution, sources, and water quality assessment.

    PubMed

    Meng, Qingpeng; Zhang, Jing; Zhang, Zhaoyu; Wu, Tairan

    2016-04-01

    Dissolved trace elements and heavy metals in the Dan River drainage basin, which is the drinking water source area of South-to-North Water Transfer Project (China), affect large numbers of people and should therefore be carefully monitored. To investigate the distribution, sources, and quality of river water, this study integrating catchment geology and multivariate statistical techniques was carried out in the Dan River drainage from 99 river water samples collected in 2013. The distribution of trace metal concentrations in the Dan River drainage was similar to that in the Danjiangkou Reservoir, indicating that the reservoir was significantly affected by the Dan River drainage. Moreover, our results suggested that As, Sb, Cd, Mn, and Ni were the major pollutants. We revealed extremely high concentrations of As and Sb in the Laoguan River, Cd in the Qingyou River, Mn, Ni, and Cd in the Yinhua River, As and Sb in the Laojun River, and Sb in the Dan River. According to the water quality index, water in the Dan River drainage was suitable for drinking; however, an exposure risk assessment model suggests that As and Sb in the Laojun and Laoguan rivers could pose a high risk to humans in terms of adverse health and potential non-carcinogenic effects. PMID:26782327

  5. Declines in dissolved silica concentrations in western Virginia streams (1988-2003): Gypsy moth defoliation stimulates diatoms?

    NASA Astrophysics Data System (ADS)

    Grady, Amy E.; Scanlon, Todd M.; Galloway, James N.

    2007-03-01

    Dissolved silica concentrations in western Virginia streams showed a significant bias toward declines (p < 0.0001) over the time period from 1988 to 2003. Streams with the greatest declines were those that had the highest mean dissolved silica concentrations, specific to watersheds underlain by basaltic and granitic bedrock. We examined potential geochemical, hydrological, and biological factors that could account for the observed widespread declines, focusing on six core watersheds where weekly stream chemistry data were available. No relationships were evident between stream water dissolved silica concentrations and pH, a finding supported by the results from a geochemical model applied to the dominant bedrock mineralogy. Along with changes in watershed acidity, changes in precipitation and discharge were also discounted since no significant trends were observed over the study period. Analyses of two longer-term data sets that extend back to 1979 revealed that the initiation of the dissolved silica declines coincided with the timing of a gypsy moth (Lymantria dispar) defoliation event. We develop a conceptual model centered on benthic diatoms, which are found within each of the six core watersheds but in greater abundance in the more silica-rich streams. Gypsy moth defoliation led to greater sunlight penetration and enhanced nitrate concentrations in the streams, which could have spurred population growth and silica uptake. The model can explain why the observed declines are primarily driven by decreased concentrations during low-flow conditions. This study illustrates lasting effects of disturbance on watershed biogeochemistry, in this case causing decadal-scale variability in stream water dissolved silica concentrations.

  6. Risk ranking of bioaccessible metals from fly ash dissolved in simulated lung and gut fluids

    SciTech Connect

    John Twining; Peter McGlinn; Elaine Loi; Kath Smith; Reto Giere

    2005-10-01

    Power plant fly ash from two fuels, coal and a mixture of coal and shredded tires were evaluated for trace metal solubility in simulated human lung and gut fluids (SLF and SGF, respectively) to estimate bioaccessibility. The proportion of bioaccessible to total metal ranged from zero (V) to 80% (Zn) for coal-derived ash in SLF and from 2 (Th) to 100% (Cu) for tire-derived fly ash in SGF. The tire-derived ash contained much more Zn. However, Zn ranked only 5th of the various toxic metals in SGF compared with international regulations for ingestion. On the basis of total concentrations, the metals closest to exceeding limits based on international regulations for inhalation were Cr, Pb, and Al. On dissolution in SLF, the most limiting metals were Pb, Cu, and Zn. For metals exposed to SGF there was no relative change in the top metal, Al, before and after dissolution but the second-ranked metal shifted from Pb to Ni. In most cases only a proportion of the total metal concentrations in either fly ash was soluble, and hence bioaccessible, in either biofluid. When considering the regulatory limits for inhalation of particulates, none of the metal concentrations measured were as hazardous as the fly ash particulates themselves. However, on the basis of the international ingestion regulations for Al, the maximum mass of fly ash that could be ingested is only 1 mg per day (10 mg based on bioaccessibility). It is possible that such a small mass could be consumed by exposed individuals or groups. 39 refs., 1 fig., 3 tabs.

  7. GROWTH AND SURVIVAL OF CHANNEL CATFISH AND YELLOW PERCH EXPOSED TO LOWERED CONSTANT AND DIURNALLY FLUCTUATING DISSOLVED OXYGEN CONCENTRATIONS

    EPA Science Inventory

    Growth and survival were determined for duplicate lots of juvenile channel catfish (Ictalurus punctatus) and yellow perch (Perca flavescens) exposed for 69 and 67 days, respectively, to nearly constant dissolved oxygen (DO) concentrations at near air saturation (control), 6.5, 5....

  8. Periodical bubble formation and the oscillatory change in dissolved oxygen concentration in a catalase-hydrogen peroxide system.

    PubMed

    Sasaki, Satoshi

    2006-06-01

    The relationship between the periodical bubble forming and the oscillatory change in the dissolved oxygen (DO) concentration in a catalase-hydrogen peroxide system was studied. Photographs of the bubbles and the responses from the DO electrode indicated that large bubbles were generated periodically, and that the DO profile depended on the geometrical relationship between the electrode and the bubbles. PMID:16772694

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

    Technology Transfer Automated Retrieval System (TEKTRAN)

    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. The determination of water quality and metal concentrations of Ampang Hilir Lake, Selangor, Peninsular Malaysia.

    PubMed

    Said, Khaled S A; Shuhaimi-Othman, M; Ahmad, A K

    2012-05-01

    A study of water quality parameters (temperature, conductivity, total dissolved solid, dissolved oxygen, pH and water hardness) in Ampang Hilir Lake was conducted in January, April, July and October 2010. The water quality parameters were tested and recorded at different sampling stations chosen randomly using Hydrolab Data Sonde 4 and Surveyor 4 a water quality multi probe (USA). Six metals which were cadmium, chromium, lead, nickel, zinc and copper were determined in five different compartments of the lake namely water, total suspended solids, plankton, sediment and fish. The metals concentration were determined by Inductively Coupled Plasma Mass Spectrometer (ICP-MS), Perkin Elmer Elan, model 9000.The water quality parameters were compared with National Water Quality Standard (NWQS Malaysia) while metal concentrations were compared with Malaysian and international standards. The study shows that water quality parameters are of class 2. This condition is suitable for recreational activities where body contact is allowed and suitable for sensitive fishing activities. Furthermore, metal concentrations were found to be lower than the international standards, therefore toxic effects for these metals would be rarely observed and the adverse effects to aquatic organisms would not frequently occur. PMID:24163953

  11. The evaluation of water quality and metal concentrations of Titiwangsa Lake, Selangor, Peninsular Malaysia.

    PubMed

    Said, Khaled S A; Shuhaimi-Othman, M; Ahmad, A K

    2012-05-15

    A study of water quality parameters (temperature, conductivity, total dissolved solid, dissolved oxygen, pH and water hardness) in Titiwangsa Lake was conducted in January, April, July and October 2010. The water quality parameters were tested and recorded at different sampling stations chosen randomly using hydrolab data sonde 4 and surveyor 4 a water quality multi probe (USA). Six metals i.e., cadmium, chromium, lead, nickel, zinc and copper were determined in five different compartments of the lake namely water, total suspended solids, plankton, sediment and fish. The metals concentration were determined by Inductively Coupled Plasma Mass Spectrometer (ICP-MS), perkin elmer elan, model 9000. The water quality parameters were compared with National Water Quality Standard (NWQS Malaysia) while metal concentrations were compared with Malaysian and international standards. The study shows that water quality parameters are of class 2. This condition is suitable for recreational activities where body contact is allowed and suitable for sensitive fishing activities. Furthermore, metal concentrations were found to be lower than the international standards, therefore toxic effects for these metals would be rarely observed and the adverse effects to aquatic organisms would not frequently occur. PMID:24187900

  12. Structurally colored biopolymer thin films for detection of dissolved metal ions in aqueous solution

    NASA Astrophysics Data System (ADS)

    Cathell, Matthew David

    Natural polymers, such as the polysaccharides alginate and chitosan, are noted sorbents of heavy metals. Their polymer backbone structures are rich in ligands that can interact with metal ions through chelation, electrostatics, ion exchange and nonspecific mechanisms. These water-soluble biopolymer materials can be processed into hydrogel thin films, creating high surface area interfaces ideal for binding and sequestering metal ions from solution. By virtue of their uniform nanoscale dimensions (with thicknesses smaller than wavelengths of visible light) polymer thin films exhibit structure-based coloration. This phenomenon, frequently observed in nature, causes the transparent and essentially colorless films to reflect light in a wide array of colors. The lamellar film structures act as one-dimensional photonic crystals, allowing selective reflection of certain wavelengths of light while minimizing other wavelengths by out-of-phase interference. The combination of metal-binding and reflective properties make alginate and chitosan thin films attractive candidates for analyte sensing. Interactions with metal ions can induce changes in film thicknesses and refractive indices, thus altering the path of light reflected through the film. Small changes in dimensional or optical properties can lead to shifts in film color that are perceivable by the unaided eye. These thin films offer the potential for optical sensing of toxic dissolved materials without the need for instrumentation, external power or scientific expertise. With the use of a spectroscopic ellipsometer and a fiber optic reflectance spectrometer, the physical and optical characteristics of biopolymer thin films have been characterized in response to 50 ppm metal ion solutions. It has been determined that metal interactions can lead to measurable changes in both film thicknesses and effective refractive indices. The intrinsic response behaviors of alginate and chitosan, as well as the responses of modified

  13. 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.

  14. EXAFS study into the speciation of metal salts dissolved in ionic liquids and deep eutectic solvents.

    PubMed

    Hartley, Jennifer M; Ip, Chung-Man; Forrest, Gregory C H; Singh, Kuldip; Gurman, Stephen J; Ryder, Karl S; Abbott, Andrew P; Frisch, Gero

    2014-06-16

    The speciation of metals in solution controls their reactivity, and this is extremely pertinent in the area of metal salts dissolved in ionic liquids. In the current study, the speciation of 25 metal salts is investigated in four deep eutectic solvents (DESs) and five imidazolium-based ionic liquids using extended X-ray absorption fine structure. It is shown that in diol-based DESs M(I) ions form [MCl2](-) and [MCl3](2-) complexes, while all M(II) ions form [MCl4](2-) complexes, with the exception of Ni(II), which exhibits a very unusual coordination by glycol molecules. This was also found in the X-ray crystal structure of the compound [Ni(phen)2(eg)]Cl2·2eg (eg = ethylene glycol). In a urea-based DES, either pure chloro or chloro-oxo coordination is observed. In [C6mim][Cl] pure chloro complexation is also observed, but coordination numbers are smaller (typically 3), which can be explained by the long alkyl chain of the cation. In [C2mim][SCN] metal ions are entirely coordinated by thiocyanate, either through the N or the S atom, depending on the hardness of the metal ion according to the hard-soft acid-base principle. With weaker coordinating anions, mixed coordination between solvent and solute anions is observed. The effect of hydrate or added water on speciation is insignificant for the diol-based DESs and small in other liquids with intermediate or strong ligands. One of the main findings of this study is that, with respect to metal speciation, there is no fundamental difference between deep eutectic solvents and classic ionic liquids. PMID:24897923

  15. Response of oxidative enzyme activities to nitrogen deposition affects soil concentrations of dissolved organic carbon

    USGS Publications Warehouse

    Waldrop, M.P.; Zak, D.R.

    2006-01-01

    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- concentration 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- concentrations in a 73-day laboratory incubation and measured microbial respiration and soil solution dissolved organic carbon (DOC) and phenolics concentrations. 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) concentrations. In the SMRO ecosystem, we observed a significant decrease in phenol oxidase activity (-73% lower limit) and an increase in soluble phenolic concentrations

  16. Dissolved-solids sources, loads, yields, and concentrations in streams of the conterminous United States

    USGS Publications Warehouse

    Anning, David W.; Flynn, Marilyn E.

    2014-01-01

    Predicted incremental loads were cascaded down through the reach network, with loads accumulating from reach to reach. For most stream reaches, the entire incremental load of dissolved solids delivered to the reach was transport

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

    NASA Astrophysics Data System (ADS)

    Tillman, Fred D.; Anning, David W.

    2014-11-01

    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.

  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. 46 CFR 148.285 - Metal sulfide concentrates.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 46 Shipping 5 2011-10-01 2011-10-01 false Metal sulfide concentrates. 148.285 Section 148.285... concentrates. (a) When information given by the shipper under § 148.60 of this part indicates that the metal sulfide concentrate may generate toxic or flammable gases, the appropriate gas detection equipment...

  20. Adsorption of Dissolved Metals in the Berkeley Pit using Thiol-Functionalized Self-Assembled Monolayers on Mesoporous Supports (Thiol-SAMMS)

    SciTech Connect

    Betancourt, Amaury P.; Mattigod, Shas V.; Wellman, Dawn M.

    2010-03-07

    The Berkeley Pit in Butte, Montana, is heavily contaminated with dissolved metals. Adsorption and extraction of these metals can be accomplished through the use of a selective adsorbent. For this research, the adsorbent used was thiol-functionalized Self-Assembled Monolayers on Mesoporous Supports (thiol-SAMMS), which was developed at Pacific Northwest National Laboratory (PNNL). Thiol-SAMMS selectively binds to numerous types of dissolved metals. The objective of this research was to evaluate the loading and kinetics of aluminum, beryllium, copper, and zinc on thiol-SAMMS. For the loading tests, a series of Berkeley Pit water to thiol-SAMMS ratios (mL:g) were tested. These ratios were 1000:1, 500:1, 100:1, and 50:1. Berkeley Pit water is acidic (pH {approx} 2.5). This can affect the performance of SAMMS materials. Therefore, the effect of pH was evaluated by conducting parallel series of loading tests wherein the Berkeley Pit water was neutralized before or after addition of thiol-SAMMS, and a series of kinetics tests wherein the Berkeley Pit water was neutralized before addition of thiol-SAMMS for the first test and was not neutralized for the second test. For the kinetics tests, one Berkeley Pit water to thiol-SAMMS ratio was tested, which was 2000:1. The results of the loading and kinetics tests suggest that a significant decrease in dissolved metal concentration at Berkeley Pit could be realized through neutralization of Berkeley Pit water. Thiol-SAMMS technology has a limited application under the highly acidic conditions posed by the Berkeley Pit. However, thiol-SAMMS could provide a secondary remedial technique which would complete the remedial system and remove dissolved metals from the Berkeley Pit to below drinking water standards.

  1. Evaluation of planning alternatives for maintaining desirable dissolved-oxygen concentrations in the Willamette River, Oregon

    USGS Publications Warehouse

    Rickert, David A.; Rinella, F.A.; Hines, W.G.; McKenzie, S.W.

    1980-01-01

    For nearly half a century the Willamette River in Oregon experienced severe dissolved-oxygen problems related to large loads of organically rich waste waters from industries and municipalities. Since the mid-1950 's dissolved oxygen quality has gradually improved owing to low-flow augmentation, the achievement of basinwide secondary treatment, and the use of other waste-management practices. As a result, summer dissolved-oxygen levels have increased, salmon runs have returned, and the overall effort is widely regarded as a singular water-quality success. To document the improved dissolved-oxygen regimen, the U.S. Geological Survey conducted intensive studies of the Willamette during the summer low-flow seasons of 1973 and 1974. During each summer the mean daily dissolved-oxygen levels were found to be higher than 5 milligrams per liter throughout the river. Because of the basinwide secondary treatment, carbonaceous deoxygenation rates were low. In addition, almost half of the biochemical oxygen demand entering the Willamette was from diffuse (nonpoint) sources rather than outfalls. These results indicated that point-source biochemical oxygen demand was no longer the primary cause of dissolved-oxygen depletion. Instead, the major causes of deoxygenation were nitrification in a shallow ' surface active ' reach below Salem and an anomalous oxygen demand (believed to be primarily of benthal origin) in Portland Harbor. (Woodard-USGS)

  2. 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. PMID:25947245

  3. Closed-loop identification and control application for dissolved oxygen concentration in a full-scale coke wastewater treatment plant.

    PubMed

    Yoo, C K; Cho, J H; Kwak, H J; Choi, S K; Chun, H D; Lee, I

    2001-01-01

    The objective of this paper is to apply a closed-loop identification to actual dissolved oxygen control system in the coke wastewater treatment plant. It approximates the dissolved oxygen dynamics to a high order model using the integral transform method and reduces it to the first-order plus time delay (FOPTD) or second-order plus time delay (SOPTD) for the PID controller tuning. To experiment the process identification on the real plant, a simple set-point change of the speed of surface aerator under the closed-loop control without any mode change was used as an activation signal of the identification. The full-scale experimental results show a good identification performance and a good tracking ability for set-point change. As a result of improved control performance, the fluctuation of dissolved oxygen concentration variation has been decreased and the electric power saving has been accomplished. PMID:11385849

  4. 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 M.

    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

  5. Henry's Law vaporization studies and thermodynamics of einsteinium-253 metal dissolved in ytterbium

    SciTech Connect

    Kleinschmidt, P.D.; Ward, J.W.; Matlack, G.M.; Haire, R.G.

    1984-07-01

    The cohesive energy of metallic einsteinium determines whether einsteinium is a trivalent or divalent metal. The enthalpy of sublimation, a measure of the cohesive energy, is calculated from the partial pressures of einsteinium over an alloy. The partial pressure of /sup 253/Es has been measured over the range 470--870 K, using combined target and mass spectrometric Knudsen effusion techniques. An alloy was prepared with einsteinium dissolved in a ytterbium solvent to produce a very dilute solution. Partial pressure measurements on the alloy were amenable to the experimental technique and a data analysis using a Henry's law treatment of the data. Vapor pressure data are combined with an estimated crystal entropy S/sup 0//sub 298/ and ..delta..C/sup 0//sub p/ for ytterbium, to produce enthalpy, entropy, and free energy functions from 298 to 1300 K. The vapor pressure of einsteinium in a dilute einsteinium--ytterbium alloy is described by the equation log P(atm) = -(6815 +- 216)/T+2.576 +- 0.337, from which we calculate for the enthalpy of sublimation of pure einsteinium ..delta..H/sup 0//sub 298/ (second law) = 31.76 kcal/mol. The value of the enthalpy of sublimation is consistent with the conclusion that Es is a divalent metal.

  6. Rates of zinc and trace metal release from dissolving sphalerite at pH 2.0-4.0

    USGS Publications Warehouse

    Stanton, M.R.; Gemery-Hill, P. A.; Shanks, Wayne C., III; Taylor, C.D.

    2008-01-01

    High-Fe and low-Fe sphalerite samples were reacted under controlled pH conditions to determine nonoxidative rates of release of Zn and trace metals from the solid-phase. The release (solubilization) of trace metals from dissolving sphalerite to the aqueous phase can be characterized by a kinetic distribution coefficient, (Dtr), which is defined as [(Rtr/X(tr)Sph)/(RZn/X(Zn) Sph)], where R is the trace metal or Zn release rate, and X is the mole fraction of the trace metal or Zn in sphalerite. This coefficient describes the relationship of the sphalerite dissolution rate to the trace metal mole fraction in the solid and its aqueous concentration. The distribution was used to determine some controls on metal release during the dissolution of sphalerite. Departures from the ideal Dtr of 1.0 suggest that some trace metals may be released via different pathways or that other processes (e.g., adsorption, solubility of trace minerals such as galena) affect the observed concentration of metals. Nonoxidative sphalerite dissolution (mediated by H+) is characterized by a "fast" stage in the first 24-30 h, followed by a "slow" stage for the remainder of the reaction. Over the pH range 2.0-4.0, and for similar extent of reaction (reaction time), sphalerite composition, and surface area, the rates of release of Zn, Fe, Cd, Cu, Mn and Pb from sphalerite generally increase with lower pH. Zinc and Fe exhibit the fastest rates of release, Mn and Pb have intermediate rates of release, and Cd and Cu show the slowest rates of release. The largest variations in metal release rates occur at pH 2.0. At pH 3.0 and 4.0, release rates show less variation and appear less dependent on the metal abundance in the solid. For the same extent of reaction (100 h), rates of Zn release range from 1.53 ?? 10-11 to 5.72 ?? 10-10 mol/m2/s; for Fe, the range is from 4.59 ?? 10-13 to 1.99 ?? 10-10 mol/m2/s. Trace metal release rates are generally 1-5 orders of magnitude slower than the Zn or Fe rates

  7. Maximizing biomass concentration in baker's yeast process by using a decoupled geometric controller for substrate and dissolved oxygen.

    PubMed

    Chopda, Viki R; Rathore, Anurag S; Gomes, James

    2015-11-01

    Biomass production by baker's yeast in a fed-batch reactor depends on the metabolic regime determined by the concentration of glucose and dissolved oxygen in the reactor. Achieving high biomass concentration in turn is dependent on the dynamic interaction between the glucose and dissolved oxygen concentration. Taking this into account, we present in this paper the implementation of a decoupled input-output linearizing controller (DIOLC) for maximizing biomass in a fed-batch yeast process. The decoupling is based on the inversion of 2×2 input-output matrix resulting from global linearization. The DIOLC was implemented online using a platform created in LabVIEW employing a TCP/IP protocol via the reactor's built-in electronic system. An improvement in biomass yield by 23% was obtained compared to that using a PID controller. The results demonstrate superior capability of the DIOLC and that the cumulative effect of smoother control action contributes to biomass maximization. PMID:26233328

  8. Understanding and modelling the variability in Dissolved Organic Carbon concentrations in catchment drainage

    NASA Astrophysics Data System (ADS)

    Coleman, Martin; Waldron, Susan; Scott, Marian; Drew, Simon

    2013-04-01

    Our knowledge of dynamic natural habitats could be improved through the deployment of automated sensor technology. Dissolved organic carbon concentrations, [DOC], are of interest to water companies as purification removes this pool and currently in environmental science, due in part to rising DOC levels and also as respiration of this C pool can lead to an increased CO2 efflux. Manual sampling of catchment drainage systems has revealed seasonal patterns in DOC (Williams, P.J.L., 1995) and that hydrological events export most DOC(Raymond, P.A. and J.E. Saiers, 2010). However, manual sampling precludes detailed characterisation of the dynamic fluctuation of DOC over shorter but important time periods e.g. immediately prior to an event; the transition from base flow to a surface run-off dominated system as surface flow pathways defrost. Such insight is only gained through deployment of continuous-monitoring equipment. Since autumn 2010 we have deployed an S::CAN Spectrolyser (which from absorbance gives a measurement of [DOC]) in a 7.5 kilometre squared peaty catchment draining Europe's largest windfarm, Whitelee. Since autumn 2011, we have an almost complete time series of [DOC] every 30. Here [DOC] has ranged from 12.2 to 58.4 mg/l C and during event flow DOC had a maximum variation of 23.5 mg/l within a single day. Simultaneously with the Spectrolyser, we have logged stage height, pH and conductivity using an In-Situ Inc MD Troll 9000. Generally there is an inverse relationship between [DOC] and both pH and conductivity, but a positive relationship (albeit with seasonal differences) with [DOC] and stage height, from which we can infer hydrological changes in the source of the DOC. Here, in addition to presenting the time series of the data, and a more accurate export budget estimate, I will explore statistical methods for the handling of large datasets. Trends in the data of such large and dynamic data sets are challenging to model. Simple relationships with stage

  9. Concentration and characteristics of dissolved carbon in the Sanjiang Plain influenced by long-term land reclamation from marsh.

    PubMed

    Guo, Y D; Lu, Y Z; Song, Y Y; Wan, Z M; Hou, A X

    2014-01-01

    Since the 1960s, the marshes in the Sanjiang Plain, Northeast China, which are an important reservoir for dissolved carbon, have undergone long-term reclamation to farmland, resulting in elevated marsh loss and degradation on a large scale. This study compared the concentrations of dissolved carbon, as well as the chemical characteristics of dissolved organic carbon (DOC), in natural marshes, a degraded marsh, and drainage ditches sampled during the growing seasons between 2008 and 2010 to clarify the temporal-spatial variability of the dissolved carbon in the fluvial system influenced by the long-term reclamation. The results show that the average concentrations of total dissolved carbon (TDC) and DOC are considerably greater in the natural marshes than in the degraded marsh and drainage ditches. The average DOC concentration for the natural marshes, approximately 35.53 ± 5.15 mg L(-1), is approximately 2.39 times that in the degraded marsh (14.84 ± 4.21 mg L(-1)) and 2.77 times the average value in the ditches (12.84 ± 4.49 mg L(-1)). The dissolved inorganic carbon (DIC) exhibits increased trends in the drainage ditches compared with the natural marshes, whereas the hydrophobic fraction of DOC is present at lower concentrations in the degraded marsh and ditches. Fluorescence indices also indicate that the DOC in the degraded marsh and ditches has a simpler humification structure. In total, the long-term reclamation has led to great variability in the DOC concentration and chemical characteristics in the fluvial system. Changes in the DOC production potential and hydrological regimes due to sustained reclamation are deemed the predominant causes of this effect. The continuously decreased DOC concentration and high variability of DOC in the surface fluvial systems are inevitable if reclamation continues in the Sanjiang Plain. More importantly, the presence of tyrosine and tryptophan-like substances in the ditches indicates that there has been extensive

  10. Analysis of environmental issues related to small-scale hydroelectric development. VI. Dissolved oxygen concentrations below operating dams

    SciTech Connect

    Cada, G.F.; Kumar, K.D.; Solomon, J.A.; Hildebrand, S.G.

    1982-01-01

    Results are presented of an effort aimed at determining whether or not water quality degradation, as exemplified by dissolved oxygen concentrations, is a potentially significant issue affecting small-scale hydropower development in the US. The approach was to pair operating hydroelectric sites of all sizes with dissolved oxygen measurements from nearby downstream US Geological Survey water quality stations (acquired from the WATSTORE data base). The USGS data were used to calculate probabilities of non-compliance (PNCs), i.e., the probabilities that dissolved oxygen concentrations in the discharge waters of operating hydroelectric dams will drop below 5 mg/l. PNCs were estimated for each site, season (summer vs remaining months), and capacity category (less than or equal to 30 MW vs >30 MW). Because of the low numbers of usable sites in many states, much of the subsequent analysis was conducted on a regional basis. During the winter months (November through June) all regions had low mean PNCs regardless of capacity. Most regions had higher mean PNCs in summer than in winter, and summer PNCs were greater for large-scale than for small-scale sites. Among regions, the highest mean summer PNCs were found in the Great Basin, the Southeast, and the Ohio Valley. To obtain a more comprehensive picture of the effects of season and capacity on potential dissolved oxygen problems, cumulative probability distributions of PNC were developed for selected regions. This analysis indicates that low dissolved oxygen concentrations in the tailwaters below operating hydroelectric projects are a problem largely confined to large-scale facilities.

  11. Distributions of dissolved trace metals (Cd, Cu, Mn, Pb, Ag) in the southeastern Atlantic and the Southern Ocean

    NASA Astrophysics Data System (ADS)

    Boye, M.; Wake, B. D.; Lopez Garcia, P.; Bown, J.; Baker, A. R.; Achterberg, E. P.

    2012-08-01

    Comprehensive synoptic datasets (surface water down to 4000 m) of dissolved cadmium (Cd), copper (Cu), manganese (Mn), lead (Pb) and silver (Ag) are presented along a section between 34° S and 57° S in the southeastern Atlantic Ocean and the Southern Ocean to the south off South Africa. The vertical distributions of Cu and Ag display nutrient-like profiles similar to silicic acid, and of Cd similar to phosphate. The distribution of Mn shows a subsurface maximum in the oxygen minimum zone, whereas Pb concentrations are rather invariable with depth. Dry deposition of aerosols is thought to be an important source of Pb to surface waters close to South Africa, and dry deposition and snowfall may have been significant sources of Cu and Mn at the higher latitudes. Furthermore, the advection of water masses enriched in trace metals following contact with continental margins appeared to be an important source of trace elements to the surface, intermediate and deep waters in the southeastern Atlantic Ocean and the Antarctic Circumpolar Current. Hydrothermal inputs may have formed a source of trace metals to the deep waters over the Bouvet Triple Junction ridge crest, as suggested by relatively enhanced dissolved Mn concentrations. The biological utilization of Cu and Ag was proportional to that of silicic acid across the section, suggesting that diatoms formed an important control over the removal of Cu and Ag from surface waters. However, uptake by dino- and nano-flagellates may have influenced the distribution of Cu and Ag in the surface waters of the subtropical Atlantic domain. Cadmium correlated strongly with phosphate (P), yielding lower Cd / P ratios in the subtropical surface waters where phosphate concentrations were below 0.95 μM. The greater depletion of Cd relative to P observed in the Weddell Gyre compared to the Antarctic Circumpolar Current could be due to increase Cd uptake induced by iron-limiting conditions in these high-nutrient-low-chlorophyll waters

  12. Distributions of dissolved trace metals (Cd, Cu, Mn, Pb, Ag) in the southeastern Atlantic and the Southern Ocean

    NASA Astrophysics Data System (ADS)

    Boye, M.; Wake, B. D.; Lopez Garcia, P.; Bown, J.; Baker, A. R.; Achterberg, E. P.

    2012-03-01

    Comprehensive synoptic datasets (surface water down to 4000 m) of dissolved cadmium (Cd), copper (Cu), manganese (Mn), lead (Pb) and silver (Ag) are presented along a section between 34° S and 57° S in the southeastern Atlantic Ocean and the Southern Ocean to the south off South Africa. The vertical distributions of Cu, Ag, and of Cd display nutrient-like profiles similar to silicic acid, and phosphate, respectively. The distribution of Mn shows a subsurface maximum in the oxygen minimum zone, whereas Pb concentrations are rather invariable with depth. Dry deposition of aerosols is thought to be an important source of Pb to surface waters close to South Africa, and dry deposition and snowfall may have been significant sources of Cu and Mn at the higher latitudes. Furthermore, the advection of water-masses enriched in trace metals following contact with continental margins appeared to be an important source of trace elements to the surface, intermediate and deep waters in the southeastern Atlantic Ocean and the Antarctic Circumpolar Current. Hydrothermal inputs appeared to have formed a source of trace metals to the deep waters over the Bouvet Triple Junction ridge crest, as suggested by relatively enhanced dissolved Mn concentrations. The biological utilization of Cu and Ag was proportional to that of silicic acid across the section, suggesting that diatoms formed an important control over the removal of Cu and Ag from surface waters. However uptake by dino- and nano-flagelattes may have influenced the distribution of Cu and Ag in the surface waters of the subtropical Atlantic domain. Cadmium correlated strongly with phosphate (P), yielding lower Cd/P ratios in the subtropical surface waters where phosphate concentrations were below 0.95 μM. The greater depletion of Cd relative to P observed in the Weddell Gyre compared to the Antarctic Circumpolar Current could be due to increase Cd-uptake induced by iron-limiting conditions in these High-Nutrient Low

  13. Assessment of dissolved Pb concentration and isotopic composition in surface waters of the modern global ocean

    NASA Astrophysics Data System (ADS)

    Pinedo-Gonzalez, P.; West, A. J.; Sanudo-Wilhelmy, S. A.

    2015-12-01

    Lead (Pb) produced by human activities, mainly from leaded gasoline combustion and high-temperature industries, dominates Pb in our present-day oceans. Previous studies have shown that surface ocean Pb concentrations and isotope ratios have varied in time and space, reflecting the changes in the amount of inputs and sources of anthropogenic Pb. However, data on surface ocean Pb is quite limited, especially for some basins like the Indian Ocean. In the present study, Pb concentrations and stable isotopes (208, 207, and 206) have been analyzed in surface water samples (3m depth) collected during the Malaspina Circumnavigation Expedition, 2010. Our results are compared with data from the literature to i) evaluate the changing status of metal contamination in surface waters of the global ocean over the last 30 years, and ii) propose potential sources of modern Pb to the oceans. Our results show that Pb concentrations in surface waters of the North Atlantic Ocean have decreased ~ 40% since 1975, attributable to the phase-out of leaded gasoline in North America. This result is corroborated by stable Pb isotope measurements. Furthermore, the isotopic gradient observed in surface waters of the studied transects in the north tropical and subtropical Atlantic Ocean can be attributed to simple mixing of European and African aerosols and Saharan Holocene loess. Results from an understudied transect in the Southern Indian Ocean give an indication of the source region of Pb delivered to this region. Although comparison with literature data is limited, mixing of Australian ores and African and Australian coals could potentially explain the measured Pb isotope composition. This study provides an opportunity to build on the work of previous oceanographic campaigns, enabling us to assess the impact of anthropogenic Pb inputs to the ocean and the relative importance of various Pb sources, providing new insights into the transport and fate of Pb in the oceans.

  14. Nucleoside-5'-phosphorothioate analogues are biocompatible antioxidants dissolving efficiently amyloid beta-metal ion aggregates.

    PubMed

    Amir, Aviran; Shmuel, Eran; Zagalsky, Rostislav; Sayer, Alon H; Nadel, Yael; Fischer, Bilha

    2012-07-28

    Amyloid beta (Aβ) peptide is known to precipitate and form aggregates with zinc and copper ions in vitro and, in vivo in Alzheimer's disease (AD) patients. Metal-ion-chelation was suggested as therapy for the metal-ion-induced Aβ aggregation, metal-ion overload, and oxidative stress. In a quest for biocompatible metal-ion chelators potentially useful for AD therapy, we tested a series of nucleoside 5'-phosphorothioate derivatives as re-solubilization agents of Cu(+)/Cu(2+)/Zn(2+)-induced Aβ-aggregates, and inhibitors of Fenton reaction in Cu(+) or Fe(2+)/H(2)O(2) system. The most promising chelator in this series was found to be APCPP-γ-S. This nucleotide was found to be more efficient than EDTA in re-solubilization of Aβ(40)-Cu(2+) aggregates as observed by the lower diameter, d(H), (86 vs. 64 nm, respectively) obtained in dynamic light scattering measurements. Likewise, APCPP-γ-S dissolved Aβ(40)-Cu(+) and Aβ(42)-Cu(2+)/Zn(2+) aggregates, as monitored by (1)H-NMR and turbidity assays, respectively. Furthermore, addition of APCPP-γ-S to nine-day old Aβ(40)-Cu(2+)/Zn(2+) aggregates, resulted in size reduction as observed by transition electron microscopy (diameter reduction from 2.5 to 0.1 μm for Aβ(40)-Cu(2+) aggregates). APCPP-γ-S proved to be more efficient than ascorbic acid and GSH in reducing OH radical production in Fe(2+)/H(2)O(2) system (IC(50) values 85, 216 and, 92 μM, respectively). Therefore, we propose APCPP-γ-S as a potential AD therapy capable of both reducing OH radical production and re-solubilization of Aβ(40/42)-M(n+) aggregates. PMID:22652964

  15. Effect of daily minimum dissolved oxygen concentration on production of channel x blue hybrid catfish

    Technology Transfer Automated Retrieval System (TEKTRAN)

    As the channel x blue hybrid catfish is stocked by an increasing number of catfish farmers, it is important to quantify the production response of this fish to pond dissolved oxygen management strategies. The purpose of this study was to quantify the production and water quality responses of the cha...

  16. 46 CFR 148.285 - Metal sulfide concentrates.

    Code of Federal Regulations, 2013 CFR

    2013-10-01

    ... 46 Shipping 5 2013-10-01 2013-10-01 false Metal sulfide concentrates. 148.285 Section 148.285... MATERIALS THAT REQUIRE SPECIAL HANDLING Special Requirements for Certain Materials § 148.285 Metal sulfide concentrates. (a) When information given by the shipper under § 148.60 of this part indicates that the...

  17. 46 CFR 148.285 - Metal sulfide concentrates.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 46 Shipping 5 2014-10-01 2014-10-01 false Metal sulfide concentrates. 148.285 Section 148.285... MATERIALS THAT REQUIRE SPECIAL HANDLING Special Requirements for Certain Materials § 148.285 Metal sulfide concentrates. (a) When information given by the shipper under § 148.60 of this part indicates that the...

  18. 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.

  19. 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

  20. Role of Dissolved Organic Matter in Sorption of Perfluorooctanoic Acid to Metal Oxides.

    PubMed

    Yang, Kai-Hsing; Ruan, Ci-Jie; Lin, Yen-Ching; Fang, Meng-Der; Wu, Chung-Hsin; Hong, Pui-Kwan Andy; Lin, Cheng-Fang

    2016-08-01

    Perfluorooctanoic acid (PFOA) is an important perfluorinated chemical of significant environmental concern. It has been widely found at high concentrations in the environment. We have exposed sediment constituent minerals SiO2, Fe2O3, and Al2O3 to PFOA and humic acid (HA) and studied the adsorption of PFOA by introducing the adsorbates in different orders. The results suggest concurrent sorption of PFOA and HA to the mineral surface or enhanced PFOA sorption when both are introduced to the aqueous phase. However, when PFOA is introduced to the mineral surface that has already been exposed to and extensively coated with HA, little PFOA adsorption occurs, which implies that PFOA released to rivers rich in dissolved organic matter (DOM, i.e. HA) may be immune to sorptive retention by the sediment and be transported downstream unabated. DOM thus can play a significant role in the transport and fate of PFOA in the natural water system. PMID:27338563

  1. Trace metal concentrations in estuaries and coastal regions

    SciTech Connect

    Hunt, C.D.

    1994-12-31

    Estuaries and coastal regions are highly variable in the physical and hydrographic conditions. As a result of heavy urbanization and industrialization of the head waters of most estuaries, there are substantial localized inputs of contaminants to the estuary. These factors combined with the flushing characteristics of individual estuaries to create relatively unique features that result in variation in the typical levels of trace metals for these systems. This makes intercomparison of the estuaries difficult. Comparability among estuaries becomes even more difficult when metals analyses are conducted without proper control of field and laboratory contamination, now firmly established in the trace metal analytical literature as a prerequisite for reliable marine trace metals analysis. This paper compares the concentrations of selected trace metal (Ag, Cd, Cu, Ni, Pb, and Zn) concentrations in the waters of several major estuaries of the United States. The basis of comparison is that all samples war collected under rigid trace metal clean collection and analysis procedures. Generally, metal concentrations within the estuaries are similar. Metal concentrations in the higher salinity coastal regions are more similar in concentration. The comparison provides a baseline of typical concentrations of these trace metals in the coastal waters against which future analytical results can be compared.

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

    USGS Publications Warehouse

    Thiros, Susan; 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

  3. ION EXCHANGE SOFTENING: EFFECTS ON METAL CONCENTRATIONS

    EPA Science Inventory

    A corrosion control pipe loop study to evaluate the effect of ion exchange water softening on metal leaching from household plumbing materials was conducted on two different water qualities having different pH's and hardness levels. The results showed that removing hardness ions ...

  4. Spatial variability in dissolved organic matter and inorganic nitrogen concentrations in a semiarid stream, San Pedro River, Arizona

    NASA Astrophysics Data System (ADS)

    Brooks, Paul D.; Lemon, Michelle M.

    2007-09-01

    We performed synoptic sampling of a 95-km reach of the San Pedro River, Arizona, to identify the effects of regional hydrology and land use on dissolved carbon and nitrogen concentrations. Six synoptic surveys, two before, two during, and two after the 2002 monsoon season, encompassed periods of both low and high stream discharge. Chloride concentrations and δ18O values during low-flow periods indicated the river was divided into three hydrologically distinct reaches each roughly 30 km long. Upper and lower reaches were characterized by areas of localized groundwater input followed by downstream evapo-concentration gradients, limited downstream solute transport, and highly variable carbon and nitrogen concentrations. In contrast, the middle reach was characterized by widespread groundwater input, continuous downstream hydrologic connectivity, and less variable carbon and nitrogen concentrations. During the monsoon season, base flow discharge increased five- to ten-fold, dissolved organic matter and inorganic N increased two- to ten-fold, Fluorescence Index (FI) values indicated a large input of terrestrial solutes, and both chloride concentrations and δ18O values indicated that stream water and alluvial groundwater were well mixed along the entire 95 km reach. Concurrently, the middle reach that exhibited continuous hydrologic connectivity during the nonmonsoon season was a net sink for N, while the reaches characterized by limited hydrologic connectivity during the low-flow season exhibited net N export. Our data suggest that instream biogeochemical cycling during the monsoon season is influenced by antecedent conditions, specifically hydrologic connectivity, during the dry season.

  5. Effects of inoculum type and bulk dissolved oxygen concentration on achieving partial nitrification by entrapped-cell-based reactors.

    PubMed

    Rongsayamanont, Chaiwat; Limpiyakorn, Tawan; Khan, Eakalak

    2014-07-01

    An entrapment of nitrifiers into gel matrix is employed as a tool to fulfill partial nitrification under non-limiting dissolved oxygen (DO) concentrations in bulk solutions. This study aims to clarify which of these two attributes, inoculum type and DO concentration 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 concentration 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 concentration 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 concentration, the preparation of entrapped cell inocula is not useful as the DO level becomes the decisive factor for achieving partial nitrification. PMID:24862001

  6. Dissolved trace elements and heavy metals in the Danjiangkou Reservoir, China

    NASA Astrophysics Data System (ADS)

    Li, Siyue; Xu, Zhifang; Cheng, Xiaoli; Zhang, Quanfa

    2008-09-01

    Concentrations of trace elements and heavy metals (Al, As, Ba, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sb, Se, Sr, V and Zn) in the Danjiangkou Reservoir, the water source area of the Middle Route of China’s interbasin South to North Water Transfer Project, were analyzed using an Inductively Coupled Plasma Atomic Emission Spectrometer (ICP-AES) and compared with the national and international standards for drinking water. The results indicated that concentrations of As, Pb, Sb and Se in the Reservoir exceeded the standards and they would pose health risk for residents in the region and the water receiving areas of the interbasin water transfer project. Spatial and temporal variability of the trace elements and heavy metals in the Reservoir implies their mixed sources of natural processing and anthropogenic activities in the upper drainage of the Reservoir. The research results would help develop water resource management and conservation strategy for the interbasin water transfer project.

  7. 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

  8. A procedure for predicting concentrations of dissolved solids and sulfate ion in streams draining areas strip mined for coal

    USGS Publications Warehouse

    Bevans, H.E.

    1980-01-01

    Current trends in increased coal production necessitate the development of techniques to appraise the environmental degradation resulting from strip mining. A procedure is introduced for the prediction of dissolved-solids and sulfate-ion concentrations in streams draining strip-mined areas. Concentrations are a function of the percentage of the drainage area that has been strip mined. These relationships are expressed by regression equations computed from data collected in streams draining strip-mined areas of Cherokee and Crawford Counties in southeast Kansas. High correlation coefficients indicate that the relationships may be useful in the evaluation of present or future strip-mining operations. (USGS)

  9. Maternal exposure to metals--concentrations and predictors of exposure.

    PubMed

    Callan, A C; Hinwood, A L; Ramalingam, M; Boyce, M; Heyworth, J; McCafferty, P; Odland, J Ø

    2013-10-01

    A variety of metals are important for biological function but have also been shown to impact health at elevated concentrations, whereas others have no known biological function. Pregnant women are a vulnerable population and measures to reduce exposure in this group are important. We undertook a study of maternal exposure to the metals, aluminium, arsenic, copper, cobalt, chromium, lithium, manganese, nickel, selenium, tin, uranium and zinc in 173 participants across Western Australia. Each participant provided a whole blood and urine sample, as well as drinking water, residential soil and dust samples and completed a questionnaire. In general the concentrations of metals in all samples were low with the notable exception of uranium (blood U mean 0.07 µg/L, range <0.01-0.25 µg/L; urinary U mean 0.018 µg/g creatinine, range <0.01-0.199 µg/g creatinine). Factors that influenced biological concentrations were consumption of fish which increased urinary arsenic concentrations, hobbies (including mechanics and welding) which increased blood manganese concentrations and iron/folic acid supplement use which was associated with decreased concentrations of aluminium and nickel in urine and manganese in blood. Environmental concentrations of aluminium, copper and lithium were found to influence biological concentrations, but this was not the case for other environmental metals concentrations. Further work is underway to explore the influence of diet on biological metals concentrations in more detail. The high concentrations of uranium require further investigation. PMID:23896418

  10. A comparison of the copper sensitivity of six invertebrate species in ambient salt water of varying dissolved organic matter concentrations.

    PubMed

    Arnold, W Ray; Cotsifas, Jeffrey S; Ogle, R Scott; Depalma, Sarah G S; Smith, D Scott

    2010-02-01

    The copper sensitivity of four saltwater invertebrates (the mussel Mytilus galloprovincialis, the oyster Crassostrea virginica, the sand dollar Dendraster excentricus, and the sea urchin Strongylocentrotus purpuratus) was determined experimentally using chronic-estimator embryo-larval test procedures. The effect of sample dissolved organic matter (DOM) content on Cu bioavailability was determined for these species using commonly prescribed test procedures. Comparisons were made among these test results and test results reported previously for two other invertebrate species: the mussel Mytilus edulis and the copepod Eurytemora affinis. All six species exhibited a direct and significant relationship between the sample dissolved organic carbon (DOC; a surrogate measure of DOM) and either the dissolved Cu median lethal concentration (LC50) values or median effect concentration (EC50) values. This relationship is significant even when the DOM has different quality as evidenced by molecular fluorescence spectroscopy. Once normalized for the effects of DOM, the Cu sensitivity of these species from least to most sensitive were E. affinis < D. excitricus < C. virginica approximately S. purpuratus approximately M. edulis approximately M. galloprovincialis. This ranking of species sensitivity differs from the saltwater species sensitivity distribution proposed in 2003 by the U.S. Environmental Protection Agency. These results support the need to account for factors that modify Cu bioavailability in future saltwater Cu criteria development efforts. More specifically, Cu saltwater species sensitivity distribution data will need to be normalized by factors affecting Cu bioavailability to assure that accurate and protective criteria are subsequently developed for saltwater species and their uses. PMID:20821449

  11. Dissolved Concentrations of PAHs and PCBs Are Often Over-predicted Using Sediment Concentrations and Literature Koc Values

    EPA Science Inventory

    There is an increasing amount of chemical and biological evidence that using sediment concentrations and commonly applied Koc values frequently overpredicts interstitial water concentrations of HOCs, and thereby overestimates uptake and/or effects of those chemicals on exposed or...

  12. 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

  13. Regulation of responsiveness of phosphorescence toward dissolved oxygen concentration by modulating polymer contents in organic-inorganic hybrid materials.

    PubMed

    Okada, Hiroshi; Tanaka, Kazuo; Chujo, Yoshiki

    2014-06-15

    Platinum(II) octaethylporphyrin (PtOEP)-loaded organic-inorganic hybrids were obtained via the microwave-assisted sol-gel condensation with methyltrimethoxysilane and poly(vinylpyrrolidone). From transparent and homogeneous hybrid films, the strong phosphorescence from PtOEP was observed. Next, the resulting hybrids were immersed in the aqueous buffer, and the emission intensity was monitored by changing the dissolved oxygen level in the buffer. When the hybrid with relatively-higher amount of the silica element, the strong phosphorescence was observed even under the aerobic conditions. In contrast, the emission from the hybrids with lower amounts of the silica element was quenched under the hypoxic conditions. This is, to the best of our knowledge, the first example to demonstrate that the responsiveness of the phosphorescence intensity of PtOEP in hybrid films to the dissolved oxygen concentration in water can be modulated by changing the percentage of the contents in the material. PMID:24794749

  14. Fiber-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof

    DOEpatents

    Janke, Christopher J; Dai, Sheng; Oyola, Yatsandra

    2014-05-13

    A fiber-based adsorbent and a related method of manufacture are provided. The fiber-based adsorbent includes polymer fibers with grafted side chains and an increased surface area per unit weight over known fibers to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. The polymer fibers include a circular morphology in some embodiments, having a mean diameter of less than 15 microns, optionally less than about 1 micron. In other embodiments, the polymer fibers include a non-circular morphology, optionally defining multiple gear-shaped, winged-shaped or lobe-shaped projections along the length of the polymer fibers. A method for forming the fiber-based adsorbents includes irradiating high surface area polymer fibers, grafting with polymerizable reactive monomers, reacting the grafted fibers with hydroxylamine, and conditioning with an alkaline solution. High surface area fiber-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

  15. A combined process of activated carbon adsorption, ion exchange resin treatment and membrane concentration for recovery of dissolved organics in pre-hydrolysis liquor of the kraft-based dissolving pulp production process.

    PubMed

    Shen, Jing; Kaur, Ishneet; Baktash, Mir Mojtaba; He, Zhibin; Ni, Yonghao

    2013-01-01

    To recover dissolved organics in pre-hydrolysis liquor (PHL) of the kraft-based dissolving pulp production process, a new combined process concept of sequential steps of activated carbon adsorption, ion exchange resin treatment, and membrane concentration, was proposed. The removal of lignin in the PHL was achieved in the activated carbon adsorption step, which also facilitates the subsequent operations, such as the membrane filtration and ion exchange resin treatment. The ion exchange resin treatment resulted in the removal/concentration of acetic acid, which opens the door for acetic acid recovery. The membrane filtration is to recover/concentrate the dissolved sugars. The combined process resulted in the production of PHL-based concentrate with relatively high concentration of hemicellulosic sugars, i.e., 22.13%. PMID:23131623

  16. The spatial distribution of dissolved and particulate heavy metals and their response to land-based inputs and tides in a semi-enclosed industrial embayment: Jiaozhou Bay, China.

    PubMed

    Wang, Changyou; Liang, Shengkang; Li, Yanbin; Li, Keqiang; Wang, Xiulin

    2015-07-01

    In order to evaluate heavy metal contamination in surface waters in the Jiaozhou Bay (JZB), a typical semi-enclosed bay in the north of China, and to identify the response of heavy metal distribution to terrigenous sources and tides, the land-based discharge flux of dissolved Cu, Pb, Zn and Cd and their particulates, as well as their concentrations, were synchronously surveyed in JZB in flood season and normal season respectively. The survey results showed that the amount of dissolved Cu clearly increased from the estuaries to the offshore waters during the flood season, especially from the Dagu estuary to the mouth of JZB. The same trend was observed for Pb. The isopleths of dissolved Zn during the flood season presented a different pattern in which a clear decrease was observed from the Lianwan, Moshui and Dagu estuaries to the offshore waters. However, the particulate Cu isopleths during the flood season, which had the same pattern as those of particulate Pb, Zn and Cd, showed a clear decrease from the Dagu estuary to the mouth of JZB. The isopleths for dissolved and particulate Cu during the normal season showed a clear decrease from the northeast to the entrance of JZB, and the same trend was observed for Pb, Zn and Cd. Observations based on synchronous investigations of the fluvial fluxes of the selected metals and their average concentrations in JZB showed that these patterns were controlled by the strong external fluvial inputs, especially from the Dagu River. The diurnal change in the Cu, Pb, Zn and Cd concentrations showed a periodicity with a cycle length of approximately 12 h in JZB, which indicates the noticeable impact of the semi-diurnal tide. The weighed average concentration from freshwater inputs calculated for dissolved Cu, Pb, Zn and Cd were higher than their average concentrations in JZB. This indicated that JZB had been contaminated with these metals, whose concentrations were also higher than those found in uncontaminated waters. PMID

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

    USGS Publications Warehouse

    Sebestyen, S.D.; Boyer, E.W.; Shanley, J.B.; Kendall, C.; Doctor, D.H.; Aiken, G.R.; Ohte, N.

    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. Copyright 2008 by the American Geophysical Union.

  18. 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.

  19. Concentrations of metals in very small volumes of soil solution

    USGS Publications Warehouse

    Hinkley, T.

    1979-01-01

    A new method of sampling very small amounts of soil solution (0.3 g) shows that soil solutions contain high concentrations and unusual proportions of metals. In the soils studied, the solution is close in both metal proportions and total metal mass to what may be taken up annually by the growth of plants at the sites sampled. Composition of soil solution varies seasonally and with depth in soil. ?? 1979 Nature Publishing Group.

  20. Modelling the migration opportunities of diadromous fish species along a gradient of dissolved oxygen concentration in a European tidal watershed

    NASA Astrophysics Data System (ADS)

    Maes, J.; Stevens, M.; Breine, J.

    2007-10-01

    The relationship between poor water quality and migration opportunities for fish remains poorly documented, although it is an essential research step in implementing EU water legislation. In this paper, we model the environmental constraints that control the movements of anadromous and catadromous fish populations that migrate through the tidal watershed of River Scheldt, a heavily impacted river basin in Western Europe. Local populations of sturgeon, sea lamprey, sea trout, Atlantic salmon, houting and allis shad were essentially extirpated around 1900. For remaining populations (flounder, three-spined stickleback, twaite shad, thinlip mullet, European eel and European smelt), a data driven logistic model was parameterized. The presence or absence of fish species in samples taken between 1995 and 2004 was modelled as a function of temperature, dissolved oxygen concentration, river flow and season. Probabilities to catch individuals from all diadromous species but three-spined stickleback increased as a function of the interaction between temperature and dissolved oxygen. The hypoxic zone situated in the freshwater tidal part of the estuary was an effective barrier for upstream migrating anadromous spawners since it blocked the entrance to historical spawning sites upstream. Similarly, habitat availability for catadromous fish was greatly reduced and restricted to lower brackish water parts of the estuary. The model was applied to infer preliminary dissolved oxygen criteria for diadromous fish, to make qualitative predictions about future changes in fish distribution given anticipated changes in water quality and to suggest necessary measures with respect to watershed management.

  1. Tolerance of Oncomelania hupensis quadrasi to varying concentrations of dissolved oxygen and organic pollution*

    PubMed Central

    Garcia, Rolando G.

    1972-01-01

    Ecological investigations were made of habitats containing natural populations of the snail Oncomelania hupensis quadrasi and of habitats free from the snail in the island of Leyte, Philippines. This species of snail is a vector of Schistosoma japonicum in the Philippines. Snail-infested habitats had dissolved oxygen levels of 3.8-9.85 ppm but snail-free habitats had levels of only 0.08-3.6 ppm. Snail-infested habitats were less polluted by organic matter than habitats that were snail-free. Larger numbers of chlorophyll-bearing algae were present in both the water and the soil of snail-infested habitats. Other factors, including temperature, pH, hydrogen carbonate alkalinity, and relative humidity, were also investigated. PMID:4538906

  2. Dissolved greenhouse gas concentrations as proxies for emissions: First results from a survey of 43 Alpine lakes

    NASA Astrophysics Data System (ADS)

    Pighini, Sylvie; Wohlfahrt, Georg; Miglietta, Franco

    2015-04-01

    Up to very recently, freshwater ecosystems were neglected in assessments of the global carbon cycle and considered merely as passive 'pipes' which transport carbon from the land to the oceans. This view has been challenged by an increasing number of studies showing that freshwater ecosystems may negate a substantial fraction of the carbon sink through carbon dioxide (CO2) and in particular methane (CH4) emissions and thus rather should be viewed as 'reactors' which process a large fraction of the terrigenous carbon. Most of our knowledge on freshwater CO2 and CH4 emissions to date derives from studies in tropical and boreal regions, while temperate freshwater ecosystems are understudied. This study is focused on lakes from the Alpine area and their content in dissolved greenhouse gases, CH4 and CO2. We mostly aim to assess the content of dissolved methane and carbon dioxide from the Alpine lakes in order to understand whether Alpine lakes could be potential CH4 and CO2 emitters. We also would like to relate concentrations to lake characteristics and potential biotic and abiotic driving forces. A diverse set of 43 lakes, from Trentino, South Tirol (Italy) and North Tirol (Austria), was selected resulting in a gradient with respect to elevation (from 240 to 1700 m a.s.l.) and latitude (from 45.52° to 47.38°). Complementary to dissolved CH4 and CO2 surface water samples, dissolved oxygen and temperature were measured. Only water surface samples were considered. Analyses were done with a gas chromatographer equipped with a flame ionization detector (FID) for CH4 and a thermal conductivity detector (TCD) for CO2 determination. The first results show that all the sampled lakes were super-saturated in dissolved methane and carbon dioxide concentrations, at least partly to a degree that in the literature has been shown to result in substantial emissions to the atmosphere. To estimate emissions, CO2 and CH4 fluxes will be quantified using the eddy covariance and floating

  3. How do changes in dissolved oxygen concentration influence microbially-controlled phosphorus cycling in stream biofilms?

    NASA Astrophysics Data System (ADS)

    Saia, S. M.; Locke, N. A.; Regan, J. M.; Carrick, H. J.; Buda, A. R.; Walter, M. T.

    2014-12-01

    Advances in molecular microbiology techniques (e.g. epi-fluorescent microscopy and PCR) are making it easier to study the influence of specific microorganisms on nutrient transport. Polyphosphate accumulating organisms (PAOs) are commonly used in wastewater treatment plants to remove excess phosphorus (P) from effluent water. PAOs have also been identified in natural settings but their ecological function is not well known. In this study, we tested the hypothesis that PAOs in natural environments would release and accumulate P during anaerobic and aerobic conditions, respectively. We placed stream biofilms in sealed, covered tubs and subjected them to alternating air (aerobic conditions) and N2 gas (anaerobic condition) bubbling for 12 hours each. Four treatments investigated the influence of changing dissolved oxygen on micribially-controlled P cycling: (1) biofilms bubbled continuously with air, (2) biofilms bubbled alternatively with air and N2, (3) biocide treated biofilms bubbled continuously with air, and (4) biocide treated biofilms bubbled alternatively with air and N2. Treatments 3 and 4 serve as abiotic controls to treatments 1 and 2. We analyzed samples every 12 hours for soluble reactive P (SRP), temperature, dissolved oxygen, and pH. We also used fluorescent microscopy (i.e. DAPI staining) and PCR to verify the presence of PAOs in the stream biofilms. SRP results over the course of the experiment support our hypothesis that anaerobic and aerobic stream conditions may impact PAO mediated P release and uptake, respectively in natural environments. The results of these experiments draw attention to the importance of microbiological controls on P mobility in freshwater ecosystems.

  4. A DFT-based toxicity QSAR study of aromatic hydrocarbons to Vibrio fischeri: Consideration of aqueous freely dissolved concentration.

    PubMed

    Wang, Ying; Yang, Xianhai; Wang, Juying; Cong, Yi; Mu, Jingli; Jin, Fei

    2016-05-01

    In the present study, quantitative structure-activity relationship (QSAR) techniques based on toxicity mechanism and density functional theory (DFT) descriptors were adopted to develop predictive models for the toxicity of alkylated and parent aromatic hydrocarbons to Vibrio fischeri. The acute toxicity data of 17 aromatic hydrocarbons from both literature and our experimental results were used to construct QSAR models by partial least squares (PLS) analysis. With consideration of the toxicity process, the partition of aromatic hydrocarbons between water phase and lipid phase and their interaction with the target biomolecule, the optimal QSAR model was obtained by introducing aqueous freely dissolved concentration. The high statistical values of R(2) (0.956) and Q(CUM)(2) (0.942) indicated that the model has good goodness-of-fit, robustness and internal predictive power. The average molecular polarizability (α) and several selected thermodynamic parameters reflecting the intermolecular interactions played important roles in the partition of aromatic hydrocarbons between the water phase and biomembrane. Energy of the highest occupied molecular orbital (E(HOMO)) was the most influential descriptor which dominated the toxicity of aromatic hydrocarbons through the electron-transfer reaction with biomolecules. The results demonstrated that the adoption of freely dissolved concentration instead of nominal concentration was a beneficial attempt for toxicity QSAR modeling of hydrophobic organic chemicals. PMID:26812082

  5. Effects of anomalous high temperatures on carbon dioxide, methane, dissolved organic carbon and trace element concentrations in thaw lakes in Western Siberia in 2012

    NASA Astrophysics Data System (ADS)

    Pokrovsky, O. S.; Shirokova, L. S.; Kirpotin, S. N.; Kulizhsky, S. P.; Vorobiev, S. N.

    2013-04-01

    During the anomalous hot summer in 2012, surface air temperatures in Western Siberia were 5 to 10 °C higher than those observed during the previous period of > 30 yr. This unusual climate phenomenon provided an opportunity to examine the effects of short-term natural heating of water in thermokarst ponds and lakes in discontinuous permafrost zones and compare these observations to previous field results obtained when the temperature was normal during the summer of 2010 in the same region. Thermokarst bodies of water shrank significantly, water levels dropped approximately 50 cm in large lakes and small (< 10-100 m2) ponds, and shallow soil depressions disappeared. Based on samples from ~ 40 bodies of water collected previously and in 2012, first-order features of changes in chemical composition in response to increased water temperatures (from 14.1 ± 2.2 to 23.8 ± 2.3 °C in 2010 and 2012, respectively) were established. In these thermokarst bodies of water that covered a full range of surface areas, the average conductivity and pH were almost unchanged, whereas dissolved organic carbon (DOC), Cl- and SO42- concentrations were higher by a factor of ~ 2 during summer 2012 compared to periods with normal temperatures. Similarly, most divalent metals and insoluble trivalent and tetravalent elements were more concentrated by a factor of 1.7-2.4 in the summer of 2012 than normal periods. The average concentrations of dissolved CO2 and CH4 during the hot summer of 2012 increased by factors of 1.4 and 4.9, respectively. For most of the trace elements bound to colloids, the degree of colloidal binding decreased by a factor of 1.44 ± 0.33 (for an average of 40 elements) during the hot summer of 2012 compared to normal periods. Increases in CO2 and CH4 concentrations with the decreasing size of the body of water were well-pronounced during the hot summer of 2012. The concentrations of CO2 and CH4 significantly increased by factors of 5 and 150, respectively, in small (

  6. Surface distribution of dissolved trace metals in the oligotrophic ocean and their influence on phytoplankton biomass and productivity

    NASA Astrophysics Data System (ADS)

    Pinedo-González, Paulina; West, A. Joshua; Tovar-Sánchez, Antonio; Duarte, Carlos M.; Marañón, Emilio; Cermeño, Pedro; González, Natalia; Sobrino, Cristina; Huete-Ortega, María.; Fernández, Ana; López-Sandoval, Daffne C.; Vidal, Montserrat; Blasco, Dolors; Estrada, Marta; Sañudo-Wilhelmy, Sergio A.

    2015-10-01

    The distribution of bioactive trace metals has the potential to enhance or limit primary productivity and carbon export in some regions of the world ocean. To study these connections, the concentrations of Cd, Co, Cu, Fe, Mo, Ni, and V were determined for 110 surface water samples collected during the Malaspina 2010 Circumnavigation Expedition (MCE). Total dissolved Cd, Co, Cu, Fe, Mo, Ni, and V concentrations averaged 19.0 ± 5.4 pM, 21.4 ± 12 pM, 0.91 ± 0.4 nM, 0.66 ± 0.3 nM, 88.8 ± 12 nM, 1.72 ± 0.4 nM, and 23.4 ± 4.4 nM, respectively, with the lowest values detected in the Central Pacific and increased values at the extremes of all transects near coastal zones. Trace metal concentrations measured in surface waters of the Atlantic Ocean during the MCE were compared to previously published data for the same region. The comparison revealed little temporal changes in the distribution of Cd, Co, Cu, Fe, and Ni over the last 30 years. We utilized a multivariable linear regression model to describe potential relationships between primary productivity and the hydrological, biological, trace nutrient and macronutrient data collected during the MCE. Our statistical analysis shows that primary productivity in the Indian Ocean is best described by chlorophyll a, NO3, Ni, temperature, SiO4, and Cd. In the Atlantic Ocean, primary productivity is correlated with chlorophyll a, NO3, PO4, mixed layer depth, Co, Fe, Cd, Cu, V, and Mo. The variables salinity, temperature, SiO4, NO3, PO4, Fe, Cd, and V were found to best predict primary productivity in the Pacific Ocean. These results suggest that some of the lesser studied trace elements (e.g., Ni, V, Mo, and Cd) may play a more important role in regulating oceanic primary productivity than previously thought and point to the need for future experiments to verify their potential biological functions.

  7. Trace metal concentrations in tropical mangrove sediments, NE Brazil.

    PubMed

    Miola, Brígida; Morais, Jáder Onofre de; Pinheiro, Lidriana de Souza

    2016-01-15

    Sediment cores were taken from the mangroves of the Coreaú River estuary off the northeast coast of Brazil. They were analyzed for grain size, CaCO3, organic matter, and trace metal (Cd, Pb, Zn, Cu, Al, and Fe) contents. Mud texture was the predominant texture. Levels of trace metals in surface sediments indicated strong influence of anthropogenic processes, and diagenetic processes controlled the trace metal enrichment of core sediments of this estuary. The positive relationships between trace metals and Al and Fe indicate that Cu, Zn, Pb, and Cd concentrations are associated mainly with Al and Fe oxy-hydroxides and have natural sources. PMID:26608507

  8. Concentration and speciation of heavy metals during water hyacinth composting.

    PubMed

    Singh, Jiwan; Kalamdhad, Ajay S

    2012-11-01

    The Tessier sequential extraction method was employed to investigate the changes in heavy metals speciation (Zn, Cu, Mn, Fe, Pb, Ni, Cd and Cr) during water hyacinth (Eichhornia crassipes) composting. Results showed that, the contents of total metals concentration were increased during the composting process. The largest proportion of metals was found in the residual fraction which was in more stable form and is consequently considered unavailable for plant uptake. Reducible and oxidizable fractions of Ni, Pb and Cd were not found in all trials during water hyacinth composting. The concentrations of Cu and Cd were very low comparative to the other metals, but the percentage of exchangeable and carbonate fractions were similar as other metals. From this study it can be concluded that the appropriate proportion of cattle manure addition (Trial 4) significantly reduced the mobile and easily available fractions (exchangeable and carbonate fractions) during the composting process. PMID:22989643

  9. Experimental whole-lake increase of dissolved organic carbon concentration produces unexpected increase in crustacean zooplankton density.

    PubMed

    Kelly, Patrick T; Craig, Nicola; Solomon, Christopher T; Weidel, Brian C; Zwart, Jacob A; Jones, Stuart E

    2016-08-01

    The observed pattern of lake browning, or increased terrestrial dissolved organic carbon (DOC) concentration, across the northern hemisphere has amplified the importance of understanding how consumer productivity varies with DOC concentration. Results from comparative studies suggest these increased DOC concentrations 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 concentration increases, we still have an incomplete understanding of how zooplankton respond to temporal increases in DOC concentration within a single system. As such, we used a whole-lake manipulation, in which DOC concentration 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 concentration 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). PMID:26919470

  10. Experimental whole-lake increase of dissolved organic carbon concentration produces unexpected increase in crustacean zooplankton density

    USGS Publications Warehouse

    Kelly, Patrick T.; Craig, Nicola; Solomon, Christopher T.; Weidel, Brian C.; Zwart, Jacob A.; Jones, Stuart E.

    2016-01-01

    The observed pattern of lake browning, or increased terrestrial dissolved organic carbon (DOC) concentration, across the northern hemisphere has amplified the importance of understanding how consumer productivity varies with DOC concentration. Results from comparative studies suggest these increased DOC concentrations 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 concentration increases, we still have an incomplete understanding of how zooplankton respond to temporal increases in DOC concentration within a single system. As such, we used a whole-lake manipulation, in which DOC concentration 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 concentration 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).

  11. 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...

  12. 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 ...

  13. Assessing metal bioavailability from cytosolic metal concentrations in natural populations of aquatic insects

    SciTech Connect

    Cain, D.J.; Luoma, S.N.; Hornberger, M.I.

    1995-12-31

    Metals occur in a variety of forms in aquatic insects. Some of these forms may be irrelevant to effects of metals on the animal, and might actually obscure links between tissue residues, metal bioavailability and toxicity (e.g. metals sorbed to external body parts, or associated with unpurged gut contents). Cytosolic metal may be a sensitive indicator of metal bioavailability and toxicity. The authors determined cytosolic metal concentrations in natural populations of the caddisfly (Trichoptera) Hydropsyche occidentalis. Cytosolic metal concentrations were compared to whole-body and sediment metal concentrations. Samples were collected along a contamination gradient over a 380 km reach of the Clark Fork River, Montana, in August of 1992 and 1993. Concentrations of cytosolic Cd, Cu, and Pb correlated with concentrations of these metals in the whole body within years. Cytosolic metals also correlated with levels of sediment contamination except at the most contaminated sites where metal concentrations in the cytosol were lower relative to sediments. The availability of Pb appeared to be low since the cytosolic Pb fraction represented less than 6% of the total Pb body burden. The cytosol contained appreciably higher proportions of the total Cd and Cu body burden than Pb. The cytosolic fraction of Cd and Cu also increased significantly between 1992 and 1993. This change reflected an increase in Cd and Cu exposure in 1993, apparently due to the mobilization of metals during higher river flows that year. The shift in cytosolic metal fractions demonstrates the dynamic nature of metal partitioning in animals in nature. These shifts can be influenced by hydrologic and geochemical conditions, as well as biological processes.

  14. Prediction of dissolved actinide concentrations in concentrated electrolyte solutions: a conceptual model and model results for the Waste Isolation Pilot Plant (WIPP)

    SciTech Connect

    Novak, C.F.; Moore, R.C.; Bynum, R.V.

    1996-10-25

    The conceptual model for WIPP dissolved concentrations is a description of the complex natural and artificial chemical conditions expected to influence dissolved actinide concentrations in the repository. By a set of physical and chemical assumptions regarding chemical kinetics, sorption substrates, and waste-brine interactions, the system was simplified to be amenable to mathematical description. The analysis indicated that an equilibrium thermodynamic model for describing actinide solubilities in brines would be tractable and scientifically supportable. This paper summarizes the conceptualization and modeling approach and the computational results as used in the WIPP application for certification of compliance with relevant regulations for nuclear waste repositories. The WIPP site contains complex natural brines ranging from sea water to 10x more concentrated than sea water. Data bases for predicting solubility of Am(III) (as well as Pu(III) and Nd(III)), Th(IV), and Np(V) in these brines under potential repository conditions have been developed, focusing on chemical interactions with Na, K, Mg, Cl, SO{sub 4}, and CO{sub 3} ions, and the organic acid anions acetate, citrate, EDTA, and oxalate. The laboratory and modeling effort augmented the Harvie et al. parameterization of the Pitzer activity coefficient model so that it could be applied to the actinides and oxidation states important to the WIPP system.

  15. The Inflammatory Phenotype in Failed Metal-On-Metal Hip Arthroplasty Correlates with Blood Metal Concentrations

    PubMed Central

    Paukkeri, Erja-Leena; Korhonen, Riku; Hämäläinen, Mari; Pesu, Marko; Eskelinen, Antti; Moilanen, Teemu; Moilanen, Eeva

    2016-01-01

    Introduction Hip arthroplasty is the standard treatment of a painful hip destruction. The use of modern metal-on-metal (MOM) bearing surfaces gained popularity in total hip arthroplasties during the last decade. Recently, worrisome failures due to adverse reaction to metal debris (ARMD), including pseudotumor response, have been widely reported. However, the pathogenesis of this reaction remains poorly understood. The aim of the present study was to investigate the ARMD response by flow cytometry approach. Methods Sixteen patients with a failed Articular Surface Replacement (ASR) hip prosthesis were included in the study. Samples of pseudotumor tissues collected during revision surgery were degraded by enzyme digestion and cells were typed by flow cytometry. Whole blood chromium and cobalt concentrations were analyzed with mass spectrometry before revision surgery. Results Flow cytometry analysis showed that the peri-implant pseudotumor tissue expressed two principal phenotypes, namely macrophage-dominated and T-lymphocyte-dominated response; the average portions being 54% (macrophages) and 25% (T-lymphocytes) in macrophage-dominated inflammation and 20% (macrophages) and 54% (T-lymphocytes) in T-lymphocyte-dominated response. The percentages of B-lymphocytes and granulocytes were lower in both phenotypes. Interestingly, the levels of blood chromium and cobalt were significantly higher in patients with macrophage-dominated response. Conclusions The results suggest that the adverse tissue reactions induced by MOM wear particles contain heterogeneous pathogeneses and that the metal levels are an important factor in the determination of the inflammatory phenotype. The present results support the hypothesis that higher metal levels cause cytotoxicity and tissue injury and macrophages are recruited to clear the necrotic debris. On the other hand, the adverse response developed in association with lower metal levels is T-lymphocyte-dominated and is likely to reflect

  16. Corrosion investigations on zircaloy-4 and titanium dissolver materials for MOX fuel dissolution in concentrated nitric acid containing fluoride ions

    NASA Astrophysics Data System (ADS)

    Jayaraj, J.; Krishnaveni, P.; Krishna, D. Nanda Gopala; Mallika, C.; Mudali, U. Kamachi

    2016-05-01

    Aqueous reprocessing of plutonium-rich mixed oxide fuels require fluoride as a dissolution catalyst in boiling nitric acid for an effective dissolution of the spent fuel. High corrosion rates were obtained for the candidate dissolver materials zircaloy-4 (Zr-4) and commercial pure titanium (CP-Ti grade 2) in boiling 11.5 M HNO3 + 0.05 M NaF. Complexing the fluoride ions either with Al(NO3)3 or ZrO(NO3)2 aided in decreasing the corrosion rates of Zr-4 and CP-Ti. From the obtained corrosion rates it is concluded that CP-Ti is a better dissolver material than Zr-4 for extended service life in boiling 11.5 M HNO3 + 0.05 M NaF, when complexed with 0.15 M ZrO(NO3)2. XPS analysis confirmed the presence of TiO2 and absence of fluoride on the surface of CP-Ti samples, indicating that effective complexation had occurred in solution leading to passivation of the metal and imparting high corrosion resistance.

  17. Influent concentrations and removal performances of metals through municipal wastewater treatment processes.

    PubMed

    Choubert, J M; Pomiès, M; Ruel, S Martin; Coquery, M

    2011-01-01

    This extensive study aimed at quantifying the concentrations and removal efficiency of 23 metals and metalloids in domestic wastewater passing through full-scale plants. Nine facilities were equipped with secondary biological treatment and three facilities were equipped with a tertiary treatment stage. The metals investigated were Li, B, Al, Ti, V, Cr, Fe, Ni, Co, Cu, Zn, As, Se, Rb, Mo, Ag, Cd, Sn, Sb, Ba, TI, Pb and U. Particulate and dissolved metals were measured using 24 h composite samples at each treatment stage. In influents, total concentrations of Cd, Sb, Co, Se, U, Ag, V were below a few microg/L, whereas at the other extremity Zn, B, Fe, Ti, Al were in the range of 0.1 to > 1 mg/L. It was demonstrated that secondary treatment stage (activated sludge, biodisc and membrane bioreactor) were efficient to remove most metals (removal rate > 70%), with the exception of B, Li, Rb, Mo, Co, As, Sb and V due to their low adsorption capacities. With the tested tertiary stages (polishing pond, rapid chemical settler, ozonation), a removal efficiency was obtained for Ti, Cr, Cd, Cu, Zn, Sn, Pb, Fe, Ag and Al, whereas a little removal (< 30%) was obtained for other metals. PMID:21902037

  18. Dissolved Hydrocarbons and related microflora in a fjordal seaport: sources, sinks, concentrations, and kinetics

    SciTech Connect

    Button, D.K.; Robertson, B.R.; Craig, K.S.

    1981-10-01

    The continuous addition of toluene as a solute of treated ballast water from oil tankers into a well-defined estuary facilitated the study of the dynamics of dissolved hydrocarbon metabolism in seawater. Near the ballast water injection point, a layer of warm ballast water, rich in bacteria, that was trapped below the less-dense fresh surface water was located. Toluene residence times were approximately 2 weeks in this layer, 2 years elsewhere in Port Valdez, and 2 decades in the surface water of a more oceanic receiving estuary adjacent. The origin of bacteria in this layer was traced to growth in oil tanker ballast during shipments. The biomass of toluene oxidizers in water samples was estimated from the average affinity of pure-culture isolates for toluene (28 liters per g of cells per h) and observed toluene oxidation kinetics. Values ranged from nearly all of the total bacterial biomass within the bacteria-rich layer down to 0.2% at points far removed. Because the population of toluene oxidizers was large with respect to the amount of toluene consumed and because water from a nearby nonpolluted estuary was equally active in facilitating toluene metabolism, we searched for an additional hydrocarbon source. It was found that terpenes could be washed from spruce trees by simulated rainfall, which suggested that riparian conifers provide an additional and significant hydrocarbon source to seawater. (JMT)

  19. 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.

  20. Risks of using membrane filtration for trace metal analysis and assessing the dissolved metal fraction of aqueous media--a study on zinc, copper and nickel.

    PubMed

    Hedberg, Yolanda; Herting, Gunilla; Wallinder, Inger Odnevall

    2011-05-01

    Membrane filtration is commonly performed for solid-liquid separation of aqueous solutions prior to trace metal analysis and when assessing "dissolved" metal fractions. Potential artifacts induced by filtration such as contamination and/or adsorption of metals within the membrane have been investigated for different membrane materials, metals, applied pressures and pre-cleaning steps. Measurements have been conducted on aqueous solutions including well-defined metal standards, ultrapure water, and on runoff water from corroded samples. Filtration using both non-cleaned and pre-cleaned filters revealed contamination and adsorption effects, in particular pronounced for zinc, evident for copper but non-significant for nickel. The results clearly show these artifacts to be non-systematic both for non-cleaned and pre-cleaned membranes. The applied pressure was of minor importance. Measurements of the labile fraction by means of stripping voltammetry clearly elucidate that membrane filtration followed by total metal analysis cannot accurately assess the labile or the dissolved metal fraction. PMID:21367497

  1. Heavy-metal concentrations in three owl species from Korea.

    PubMed

    Kim, Jungsoo; Lee, Hang; Koo, Tae-Hoe

    2008-01-01

    This study presents concentrations of heavy metals (iron, zinc, manganese, copper, lead, and cadmium) in livers of three owl species from Korea. Essential trace elements (iron, zinc, manganese, and copper) did not differ among the owl species. We suggest that the essential elements are within the normal range and are maintained by normal homeostatic mechanisms. Lead and cadmium concentrations in Eurasian Eagle Owls (Bubo bubo) were significantly lower than in Brown Hawk Owls (Nixos scutulata) and Collared Scops Owls (Otus lempiji). Lead and cadmium concentrations in Korean owl species were at background levels; lead concentrations in two Collared Scops Owls were above background concentrations. Lead and cadmium concentrations were similar to concentrations previously reported in owls from other parts of the world. We suggest that lead and cadmium concentrations in Korean owls are below toxic concentrations. PMID:17955366

  2. Spatial and Seasonal Variation of Dissolved Organic Carbon (DOC) Concentrations in Irish Streams: Importance of Soil and Topography Characteristics

    NASA Astrophysics Data System (ADS)

    Liu, Wen; Xu, Xianli; McGoff, Nicola M.; Eaton, James M.; Leahy, Paul; Foley, Nelius; Kiely, Gerard

    2014-05-01

    Dissolved organic carbon (DOC) concentrations have increased in many sites in Europe and North America in recent decades. High DOC concentrations can damage the structure and functions of aquatic ecosystems by influencing water chemistry. This study investigated the spatial and seasonal variation of DOC concentrations in Irish streams across 55 sites at seven time occasions over 1 year (2006/2007). The DOC concentrations ranged from 0.9 to 25.9 mg/L with a mean value of 6.8 and a median value of 5.7 mg/L and varied significantly over the course of the year. The DOC concentrations from late winter (February: 5.2 ± 3.0 mg/L across 55 sites) and early spring (April: 4.5 ± 3.5 mg/L) had significantly lower DOC concentrations than autumn (October: mean 8.3 ± 5.6 mg/L) and early winter (December: 8.3 ± 5.1 mg/L). The DOC production sources (e.g., litterfall) or the accumulation of DOC over dry periods might be the driving factor of seasonal change in Irish stream DOC concentrations. Analysis of data using stepwise multiple linear regression techniques identified the topographic index (TI, an indication of saturation-excess runoff potential) and soil conditions (organic carbon content and soil drainage characteristics) as key factors in controlling DOC spatial variation in different seasons. The TI and soil carbon content (e.g., soil organic carbon; peat occurrence) are positively related to DOC concentrations, while well-drained soils are negatively related to DOC concentrations. The knowledge of spatial and seasonal variation of DOC concentrations in streams and their drivers are essential for optimum riverine water resources management.

  3. Change of dissolved gaseous mercury concentrations in a southern reservoir lake (Tennessee) following seasonal variation of solar radiation.

    PubMed

    Zhang, Hong; Dill, Christopher; Kuiken, Todd; Ensor, Melissa; Crocker, William Chad

    2006-04-01

    A 12-month field study was conducted consecutively from June 2003 to May 2004 to quantify temporal variations of dissolved gaseous mercury (DGM) concentrations in Cane Creek Lake, a southern reservoir lake (Cookeville, TN). Diurnal changes of DGM concentrations in two periods (morning increase vs afternoon decrease with an around-noon peak) were observed, and the changes closely followed daily solar radiation variation trends. The diurnal patterns prevailed in the late spring and summer, but became vague in the late fall and winter. The monthly mean DGM concentrations peaked at 40.8 pg L(-1) in July and reached the lowest at 14.2 pg L(-1) in December and 21.9 pg L(-1) in January; this DGM concentration change closely followed the monthly mean solar radiation variation trend. The increase of the lake DGM concentration from January to July and its decrease from July to December mirror the typical daily rhythm of DGM concentration variations in the two periods. This finding supports the following hypothesis: The natural phenomenon of daily oscillation of freshwater DGM concentrations that follows diurnal solar radiation variation would manifest on a seasonal scale. High DGM concentrations were found in the spring and summer and low in the fall and winter (seasonal mean: 34.2, 37.5, 20.0, 24.4 pg L(-1), respectively). This seems to suggest an annual occurrence of two periods of the seasonal DGM level fluctuation (spring and summer high vs fall and winter low DGM levels). Linear relationships of the monthly mean DGM concentrations were found with the monthly mean global solar radiation (R2 = 0.82, P < 0.05) and UVA radiation (R2 = 0.84, P < 0.05). Linear relationships of the seasonal mean DGM concentrations were also found with the seasonal mean global solar radiation (R2 = 0.85, P = 0.08) and UVA radiation (R2 = 0.93, P < 0.05). PMID:16646441

  4. 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

  5. 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. PMID:27149152

  6. Use of pore-water composition to reconstruct past dissolved inorganic carbon concentration and alkalinity in Pacific bottom water

    NASA Astrophysics Data System (ADS)

    Sauvage, J. F.; Spivack, A. J.; D'Hondt, S. L.; Integrated Ocean Drilling Program Expedition 329 shipboard scientific party

    2011-12-01

    The carbonate system is a crucial component in controlling the pH of the world's oceans and the distribution of CO2 within the ocean, as well as between the ocean and atmosphere. Consequently, dissolved inorganic carbon (DIC) and alkalinity reconstructions bear lots of promise for improving understanding of the ocean's role in the global carbon cycle and climate. We propose and test a method to quantify in situ concentrations of deep-sea carbonate-system components (DIC, alkalinity, CO32-, Ca2+, and minor component concentrations) in pore fluid of deep-sea sediment cores. These concentrations can in turn be used to reconstruct deep-sea carbonate-system chemistry of the geologic past. Alkalinity, DIC and Ca2+ concentrations measured on research vessels differ from in situ values because temperature and pressure changes during core recovery, storage and extraction induce calcium carbonate precipitation and in this way alter the original composition. To reconstruct in situ values, we developed a method that takes advantage of the mathematically over-determined state of the system if three components are measured, given that CaCO3 is saturated and the dissolved carbonate system is at equilibrium in situ. As a result, based on the measured alkalinity, DIC and Ca2+ concentrations, in situ CO2aq, HCO3-, CO32-, and minor species concentrations are calculated by applying an iteration process. This approach allows us to calculate the amount of CaCO3 precipitated during sediment recovery from the seafloor, and hence in situ carbonate system components. We apply our model to pore-water data from two SPG sites rich in calcium carbonate and drilled by Integrated Ocean Drilling Program Expedition 329 (Sites 1367 and 1368). We compared two sample types for this study, (i) samples squeezed and processed within minutes of recovery (rapidly processed) and (ii) samples processed in the following hours/days, and as consequence prone to some substantial alteration (slowly processed

  7. Analyzing freely dissolved concentrations of cationic surfactant utilizing ion-exchange capability of polyacrylate coated solid-phase microextraction fibers.

    PubMed

    Chen, Yi; Droge, Steven T J; Hermens, Joop L M

    2012-08-24

    A 7-μm polyacrylate (PA) coated fiber was successfully employed to determine freely dissolved concentrations of cationic surfactants by solid-phase microextraction (SPME) and utilizing the capability of the PA-coating to sorb organic cations via ion-exchange at carboxylic groups. Measured fiber-water partitioning coefficients (K(fw)) were constant below a fiber loading of 2mmol per liter polyacrylate, allowing for simple and accurate analysis in a concentration range that is relevant from a risk assessment point of view. Ion-exchange was confirmed to be the main sorption mechanism because of a decreasing K(fw) with either higher CaCl(2) concentrations or lower pH, and maximum fiber uptake at the polyacrylate cation-exchange capacity (CEC, at 30mmol/L PA). Fiber-water sorption isotherms were established in various aqueous media in toxicological relevant concentrations. The developed SPME method has a high potential for application in ecotoxicological studies, as demonstrated in sorption studies with humic acid in different electrolyte solutions at aqueous concentrations down to the sub nM range. Cationic surfactant sorption affinities for humic acid also depend on medium composition but are orders of magnitude higher than to the PA fiber on a sorbent weight basis. PMID:22818738

  8. River bank restoration effects on dissolved organic carbon concentrations in groundwater during floods

    NASA Astrophysics Data System (ADS)

    Derx, J.; Blaschke, A. P.

    2012-04-01

    Estimating the effect of river restoration on groundwater quality is important in the view of nationwide implementations demanded by e.g. the EU Water Framework Directive. DOC transport during river infiltration conditions was examined based on 3D flow and contaminant transport simulations with transient groundwater-surface water interaction. In a scenario setting the effects of river restoration on DOC concentrations, travel time and distance from the river required for DOC reduction in groundwater during river floods were investigated. River restoration was assumed to cause scouring of the riverbank, which a) affects the bank geometry and provides more chance of the river to interact with groundwater and b) reduces bank sediment clogging. A shallow unconfined alluvial aquifer of gravel and sandy gravel media was assumed which was either well connected to the river or was confined by a thin clogging layer at the top of the river bed and bank at natural infiltration conditions. Scenario results showed that riverbank restoration facilitates DOC transport into the aquifer during floods. Even if riverbank permeability remained unchanged, floods caused significantly higher DOC concentrations at a restored than at a channelised riverbank. At the same time, DOC concentration peaks in groundwater arrived earlier and the required distance from the river reducing DOC to background concentrations increased. These effects were explained by changes in bank geometry, and thus a greater ability of the river to interact with groundwater.

  9. DISTRIBUTION OF FINGERLING BROOK TROUT, SALVELINUS FONTINALIS (MITCHELL), IN DISSOLVED OXYGEN CONCENTRATION GRADIENTS

    EPA Science Inventory

    A self-recording linear gradient tank and procedures are described in which individual brook trout fingerlings unstressed by recent transfer, unaccustomed surroundings or the presence of an observer could move freely in 16 oxygen concentration gradients within the limits of 1 and...

  10. Adsorption as a control of metal concentrations in sediment extracts

    SciTech Connect

    Rendell, P.S.; Batley, G.E.; Cameron, A.J.

    1980-03-01

    The adsorption of Cu, Pb, and Cd from selected extractant solutions, onto uncontaminated river sediments, has been investigated under typical extraction conditions. Significant adsorption of added metal was found to occur during overnight extraction with dilute HCl (pH>1.5), 0.1 M hydroxylamine hydrochloride (pH 2), 0.1 M sodium citrate (pH 4.6), 1 M ammonium acetate, 10% sodium citrate-1% sodium dithionite, and 25% acetic acid. Adsorption also occurred during a hydrogen peroxide digestion procedure. The inability of reagents to prevent losses of soluble metal in these experiments strongly suggests that a proportion of the metal actually released from a sediment sample during an extraction will be readsorbed. This may lead to serious misinterpretation of extraction data because the metal concentrations determined in the extract do not represent metal levels in the sediment fractions attacked.

  11. Biomineralization of metal-containing ores and concentrates.

    PubMed

    Rawlings, Douglas E; Dew, David; du Plessis, Chris

    2003-01-01

    Biomining is the use of microorganisms to extract metals from sulfide and/or iron-containing ores and mineral concentrates. The iron and sulfide is microbially oxidized to produce ferric iron and sulfuric acid, and these chemicals convert the insoluble sulfides of metals such as copper, nickel and zinc to soluble metal sulfates that can be readily recovered from solution. Although gold is inert to microbial action, microbes can be used to recover gold from certain types of minerals because as they oxidize the ore, they open its structure, thereby allowing gold-solubilizing chemicals such as cyanide to penetrate the mineral. Here, we review a strongly growing microbially-based metal extraction industry, which uses either rapid stirred-tank or slower irrigation technology to recover metals from an increasing range of minerals using a diversity of microbes that grow at a variety of temperatures. PMID:12480349

  12. [Characteristics of Dissolved CH₄ and N₂O Concentrations of Weihe River in Xinxiang Section in Spring].

    PubMed

    Hou, Cui-cui; Zhang, Fang; Li, Ying-chen; Wang, Qi-bo; Liu, Sai

    2016-05-15

    Distributions of CH₄ and N₂O concentrations 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 concentrations (P < 0.01), but in the new district, dissolved N₂O concentration 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 concentrations could be explained by NH₄⁺-N concentrations and water temperature, and CH₄ concentrations in the surface water of Weihe River was significantly correlated with NH₄⁺-N concentrations (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 concentrations would be positively correlated, indicating that different nitrogen sources would impact the coupling mechanism of CH₄and N₂O productions. PMID:27506045

  13. Variations in concentrations and fluxes of dissolved inorganic nutrients related to catchment scale human interventions in Pamba River, Kerala, India

    NASA Astrophysics Data System (ADS)

    David, S. E.; Jennerjahn, T. C.; Chattopadhyay, S.

    2012-12-01

    River basins are geo-hydrological units. Water flowing out of the basin bears the imprint of natural factors such as geology, soil, vegetation and rainfall along with anthropogenic factors including the type and degree of human intervention within the basin. Pamba, a small mountainous river in the SW coast of India with a population density of ~1,400 persons km-2 was studied for its varying land use and human interventions as the global database are biased towards temperate regions while little is know about the smaller catchments from tropical regions. Land use comprised of dense forest in the highland region together with forest plantation and the human impacted Sabarimala temple- the second largest pilgrim, settlement with mixed tree crop (smt) in the midland and lowland paddy cultivated region. 50-60 million devotees visiting Sabarimala during November to January every year associated with the ritual bathing, discharge of human wastes emanating from the influx of millions of pilgrims due to inadequate number of sanitary latrines and the lack of facilities for sewage collection and treatment caused several ecological variations during pilgrim season. In order to asses the effect of land use and pilgrims in combination with seasonal variations in hydrology we investigated the seasonal and spatial variations in physicochemical and nutrient concentrations. Samples were collected from March 2010 to February 2012 during premonsoon (January-May), SW(June to September) and NE monsoon(October to December), from sites varying in land use. Nutrient budgets (load and yield) were calculated to quantify the inputs from various land use segments. Spatio-temporal variations in the physicochemical and dissolved nutrient concentrations were observed along the course of the river. Upstream forest region had highest dissolved oxygen(DO) and pH together with lowest dissolved inorganic nitrogen(DIN) values indicating almost pristine conditions. DIN in the temple region had the

  14. PHOTOCHEMICAL ALTERATION OF DISSOLVED ORGANIC MATTER: EFFECTS ON THE CONCENTRATION AND ACIDITIES OF IONIZABLE SITES IN DISSOLVED ORGANIC MATTER IN THE SATILLA RIVER OF GEORGIA, USA

    EPA Science Inventory

    The acid-base properties of humic substances, the major component of dissolved 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 ...

  15. In situ Raman-based measurements of high dissolved methane concentrations in hydrate-rich ocean sediments

    NASA Astrophysics Data System (ADS)

    Zhang, Xin; Hester, Keith C.; Ussler, William; Walz, Peter M.; Peltzer, Edward T.; Brewer, Peter G.

    2011-04-01

    Ocean sediment dissolved CH4 concentrations 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 dissolved 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.

  16. Heavy Metal Concentrations in Soils Downwind from Masaya Volcano (Nicaragua)

    NASA Astrophysics Data System (ADS)

    Delfosse, T.; Delmelle, P.; Iserentant, A.; Delvaux, B.

    2003-12-01

    Quiescently degassing volcanoes can significantly contribute to the global emission of heavy metals. In turn, substantial deposition of metals onto soils may result, possibly increasing the risk of phytotoxicity. In contrast to anthropogenic sources, the environmental impacts of airborne volcanic heavy metals and their accumulation in soils are poorly studied. Along with the degassing of S, Cl and F, Masaya volcano, Nicaragua, is also a strong source of heavy metals. Recent estimates indicate emission rates of e.g., 62 t As yr-1, 133 t Zn yr-1 and 306 t Cu yr-1 (Moune, 2002). Here, we report on the effects of heavy metal depositions on the total contents of As, Cr, Ni, Cu, Bi, Zn, Se, and Co in two groups of soils located 5 km and 15 km downwind from the volcano. These soils correspond to young Vitric Andosols and more weathered Eutric Andosols, respectively. As and Se were measured by Inductively Coupled Plasma-Atomic Emission Spectrometry after soil digestion in a trace metal unit, and Cr, Ni, Cu, Co, Bi and Zn were determined after alkaline fusion in Li-metaborate/Li-tetraborate. Results suggest that prolonged metal inputs in the vicinity of Masaya volcano have significantly increased the As, Se and Zn contents of the soils. For these elements, concentrations are about 3-5 times those measured in the parent rock materials. However, maximum concentrations in soils (i.e., 5.4 mg As kg-1, 183 mg Zn kg-1 and 0.9 mg Se kg-1) never exceed critical concentration levels as defined for cultivated soils in the UK (10, 300 and 3 mg kg-1 for As, Zn and Se, respectively). We did not detect significant enrichments in Cr, Ni, Cu, Bi, and Co. The relatively low accumulation of metals in the Masaya Andosols contrasts with the high retention of volcanic F and S inputs (Delmelle et al., 2003). Since Andosols typically show a high affinity for heavy metals, which can be bound to organic matter as well as to oxides, oxyhydroxide and allophane minerals present in these soils, rapid

  17. Monitoring metal concentrations in tissues and single cells using ultramicrosensors.

    PubMed Central

    Malinski, T; Grunfeld, S; Taha, Z; Tomboulian, P

    1994-01-01

    Intercellular and extracellular metal concentrations were measured using carbon fiber ultramicrosensors plated with mercury or with polymeric porphyrinic p-type semiconductors. Concentrations of unbound nickel and lead ions were studied within individual BC3H-1 myocytes, and H4-11-C3 rat hepatoma cells. Unbound ions are predominantly solvated inorganic ions not coordinated to biological cellular components. Fabrication of ultramicrosensors appropriate for the cells under investigation is described, including procedures for sharpening and waxing the microsensors in order to control the shape, area, and dimensions of the electroactive surface. Metal ion movement through cell membranes and intracellular ion diffusion in aorta tissue were studied. Images Figure 2. PMID:7843090

  18. Heavy metal concentrations in tissues of Virginia river otters

    SciTech Connect

    Anderson-Bledsoe, K.L.; Scanlon, P.F.

    1983-04-01

    Concentrations of lead, cadmium, zinc and copper in liver, kidney and bone samples of otter harvested during the 1979-1980 and 1980-1981 trapping seasons were determined by atomic absorption spectrophotometry. Correlations between metal concentrations and age for all three tissues were nonsignificant. Correlations among the concentrations of the four elements in liver and kidney samples were also nonsignificant for otter samples in both years. The highest correlation coefficient (0.47) was found between zinc and copper concentrations in liver samples from otters trapped during the 1979-1980 trapping season. (JMT)

  19. [Concentration and Source of Dissolved Organic Carbon in Snowpits of the Tibetan Plateau].

    PubMed

    Yan, Fang-ping; Kang, Shi-chang; Chen, Peng-fei; Bai, Jian-kun; Li, Yang; Hu, Zhao-fu; Li, Chao-liu

    2015-08-01

    Snowpit samples of three glaciers (Laohugou NO. 12 Glacier (LHG), Small Dongkemadi Glacier on Mount Tanggula (TGL) and East Ronghuk Glacier on Mount Everest (ZF)) in the Tibetan Plateau were collected. Concentrations of DOC and major ions were analyzed. The results showed that average DOC concentrations of the snowpits of LHG, TGL and ZF were (250.30 +/- 157.10), (216.92 +/- 142.82) and (152.50 +/- 56.11) microg x L(-1), respectively. DOC of TGL and ZF accounted for large parts of total values of DOC and ions. Correspondingly, DOC of LHG accounted for small part (only 5%), because LHG was located at north China and intensively influenced by natural mineral dust, which caused high concentrations of Ca2+ (the highest value could reach 5299.18 microg x L(-1)) and consequently low percentage of DOC of snowpit samples. Correlation and PCA analyses were used to study the sources of DOC. DOC was significantly correlated with Ca2+, Mg2+, K+ and SO4(2-). Additionally, PCA further indicated that the main potential source of DOC was the natural source of mineral dust. Meanwhile, anthropogenic pollutants (e.g., biomass, fossil combustion and agricultural related pollutants) could also not be ignored. Moreover, the carbon depositional fluxes of three snowpits were roughly estimated, and the values of LHG, TGL and ZF snowpits were 189.23, 132.76 and 128.44 mg (m2 x a)(-1), respectively, which played a significant role in the carbon cycle in this region and was also helpful for the study of glaciers fluctuation. PMID:26592009

  20. One year of Seaglider dissolved oxygen concentration profiles at the PAP site

    NASA Astrophysics Data System (ADS)

    Binetti, Umberto; Kaiser, Jan; Heywood, Karen; Damerell, Gillian; Rumyantseva, Anna

    2015-04-01

    Oxygen is one of the most important variables measured in oceanography, influenced both by physical and biological factors. During the OSMOSIS project, 7 Seagliders were used in 3 subsequent missions to measure a multidisciplinary suite of parameters at high frequency in the top 1000 m of the water column for one year, from September 2012 to September 2013. The gliders were deployed at the PAP time series station (nominally at 49° N 16.5° W) and surveyed the area following a butterfly-shaped path. Oxygen concentration was measured by Aanderaa optodes and calibrated using ship CTD O2 profiles during 5 deployment and recovery cruises, which were in turn calibrated by Winkler titration of discrete samples. The oxygen-rich mixed layer deepens in fall and winter and gets richer in oxygen when the temperature decreases. The spring bloom did not happen as expected, but instead the presence of a series of small blooms was measured throughout spring and early summer. During the summer the mixed layer become very shallow and oxygen concentrations decreased. A Deep Oxygen Maximum (DOM) developed along with a deep chlorophyll maximum during the summer and was located just below the mixed layer . At this depth, phytoplankton had favourable light and nutrient conditions to grow and produce oxygen, which was not subject to immediate outgassing. The oxygen concentration in the DOM was not constant, but decreased, then increased again until the end of the mission. Intrusions of oxygen rich water are also visible throughout the mission. These are probably due to mesoscale events through the horizontal transport of oxygen and/or nutrients that can enhance productivity, particularly at the edge of the fronts. We calculate net community production (NCP) by analysing the variation in oxygen with time. Two methods have been proposed. The classical oxygen budget method assumes that changes in oxygen are due to the sum of air-sea flux, isopycnal advection, diapycnal mixing and NCP. ERA

  1. Basin-scale transport of hydrothermal dissolved metals across the South Pacific Ocean.

    PubMed

    Resing, Joseph A; Sedwick, Peter N; German, Christopher R; Jenkins, William J; Moffett, James W; Sohst, Bettina M; Tagliabue, Alessandro

    2015-07-01

    Hydrothermal venting along mid-ocean ridges exerts an important control on the chemical composition of sea water by serving as a major source or sink for a number of trace elements in the ocean. Of these, iron has received considerable attention because of its role as an essential and often limiting nutrient for primary production in regions of the ocean that are of critical importance for the global carbon cycle. It has been thought that most of the dissolved iron discharged by hydrothermal vents is lost from solution close to ridge-axis sources and is thus of limited importance for ocean biogeochemistry. This long-standing view is challenged by recent studies which suggest that stabilization of hydrothermal dissolved iron may facilitate its long-range oceanic transport. Such transport has been subsequently inferred from spatially limited oceanographic observations. Here we report data from the US GEOTRACES Eastern Pacific Zonal Transect (EPZT) that demonstrate lateral transport of hydrothermal dissolved iron, manganese, and aluminium from the southern East Pacific Rise (SEPR) several thousand kilometres westward across the South Pacific Ocean. Dissolved iron exhibits nearly conservative (that is, no loss from solution during transport and mixing) behaviour in this hydrothermal plume, implying a greater longevity in the deep ocean than previously assumed. Based on our observations, we estimate a global hydrothermal dissolved iron input of three to four gigamoles per year to the ocean interior, which is more than fourfold higher than previous estimates. Complementary simulations with a global-scale ocean biogeochemical model suggest that the observed transport of hydrothermal dissolved iron requires some means of physicochemical stabilization and indicate that hydrothermally derived iron sustains a large fraction of Southern Ocean export production. PMID:26156374

  2. Basin-scale transport of hydrothermal dissolved metals across the South Pacific Ocean

    NASA Astrophysics Data System (ADS)

    Resing, Joseph A.; Sedwick, Peter N.; German, Christopher R.; Jenkins, William J.; Moffett, James W.; Sohst, Bettina M.; Tagliabue, Alessandro

    2015-07-01

    Hydrothermal venting along mid-ocean ridges exerts an important control on the chemical composition of sea water by serving as a major source or sink for a number of trace elements in the ocean. Of these, iron has received considerable attention because of its role as an essential and often limiting nutrient for primary production in regions of the ocean that are of critical importance for the global carbon cycle. It has been thought that most of the dissolved iron discharged by hydrothermal vents is lost from solution close to ridge-axis sources and is thus of limited importance for ocean biogeochemistry. This long-standing view is challenged by recent studies which suggest that stabilization of hydrothermal dissolved iron may facilitate its long-range oceanic transport. Such transport has been subsequently inferred from spatially limited oceanographic observations. Here we report data from the US GEOTRACES Eastern Pacific Zonal Transect (EPZT) that demonstrate lateral transport of hydrothermal dissolved iron, manganese, and aluminium from the southern East Pacific Rise (SEPR) several thousand kilometres westward across the South Pacific Ocean. Dissolved iron exhibits nearly conservative (that is, no loss from solution during transport and mixing) behaviour in this hydrothermal plume, implying a greater longevity in the deep ocean than previously assumed. Based on our observations, we estimate a global hydrothermal dissolved iron input of three to four gigamoles per year to the ocean interior, which is more than fourfold higher than previous estimates. Complementary simulations with a global-scale ocean biogeochemical model suggest that the observed transport of hydrothermal dissolved iron requires some means of physicochemical stabilization and indicate that hydrothermally derived iron sustains a large fraction of Southern Ocean export production.

  3. Influence of environmental parameters on the concentration of subsurface dissolved methane in two hydroelectric power plants in Brazil

    NASA Astrophysics Data System (ADS)

    Silva, M. G.; Marani, L.; Alvala, P. C.

    2013-12-01

    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 dissolved 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 concentration. 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 dissolved 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 dissolved 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 concentration of dissolved methane was evaluated by multivariate statistical techniques (Principal Component Analysis - PCA). All of the parameters had some correlation with dissolved 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

  4. Statistical evaluation of biogeochemical variables affecting spatiotemporal distributions of multiple free metal ion concentrationsin an urban estuary

    EPA Science Inventory

    Free metal ion concentrations have been recognized as a better indicator of metal bioavailability in aquatic environments than total dissolved metal concentrations. However, our understanding of the determinants of free ion concentrations, especially in a metal mixture, is limite...

  5. Direct analysis of δ13C and concentration of dissolved organic carbon (DOC) in environmental samples by TOC-IRMS

    NASA Astrophysics Data System (ADS)

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

    2014-05-01

    Dissolved 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 concentration 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 concentration 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 concentrations 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 concentration measurements. Assessment of natural abundance and slightly 13C enriched DOC, a wide range of concentrations (0.2-150 mgC/L) and injection volumes (0.05-3 ml), demonstrated good analytical performance with negligible memory effects, no concentration/volume effects and a wide linearity. Low DOC concentrations (< 2 mgC/L), were correctly analyzed without any pre-concentration. Moreover, TOC-IRMS was successfully applied to analyze DOC from diverse terrestrial, freshwater and marine environments (SD < 0.23 permil). In summary, the TOC

  6. Storage mediums affect metal concentration in woodlice (Isopoda).

    PubMed

    Hendrickx, Frederik; Maelfait, Jean-Pierre; De Mayera, Ann; Tack, Filip M G; Verloo, Marc G

    2003-01-01

    Terrestrial invertebrates are becoming widely established as tools to assess heavy metal pollution at contaminated sites. A practical and time saving method to sample terrestrial invertebrates consist of pitfall traps, often filled with a 4% formaldehyde solution and some detergent. The reliability of metal concentrations based on organisms captured and stored in this solution might however be questioned and we therefore tested the effect of formaldehyde on Zn, Cu, Cd and Pb concentration experimentally in three isopod species. Our results showed that in many cases, significant decreases in Cu concentrations compared to animals stored in a freezer were observed that could be as high as 40%, while Zn, Cd and Pb concentrations increased. A regression analysis of individual dry weight on individual size revealed that formaldehyde decreases the dry weight substantially and in that way causes increased measurements of Zn, Cd and Pb concentrations. We conclude that pitfall traps with formaldehyde should better not be used to collect animals in which concentrations of heavy metals or other toxic substances will be determined. PMID:12475065

  7. Concentration of some platinum-group metals in coal

    USGS Publications Warehouse

    Finkelman, R.B.; Aruscavage, P. J.

    1981-01-01

    New data on some platinum group metals in coal indicate that the concentration of Pt is generally less than about 5 ppb, that of Pd is generally less than 1 ppb, and that of Rh is generally less than 0.5 ppb. No conclusive evidence was obtained concerning the mode of occurrence of these elements in coal. ?? 1981.

  8. Benthic invertebrates, periphyton, and bottom material and their trace-metal concentrations in Salmon Creek basin, Clark County, Washington

    USGS Publications Warehouse

    White, Amy C.; McKenzie, Stuart W.

    1979-01-01

    In 1978, data were collected for identification and quantification of benthic invertebrates, periphyton, and bottom material and their trace-metals concentrations from three sites in Salmon Creek basin, Wash. Metal analyses included arsenic, cadmium, chromium, copper, lead, zinc, selenium, and mercury. Physical data collected included water temperature, dissolved oxygen, pH, discharge, and size of cobbles and fine stream-bottom material. Additional chemical analyses included major constituents. Benthic invertebrate identifications were generally taken to the generic level, with a total of 49 taxons identified and quantified. A total of 36 periphyton taxons were quantified and identified, generally at the species level. 

  9. Benthic invertebrates, periphyton, and bottom material and their trace-metal concentrations in Salmon Creek basin, Clark County, Washington

    USGS Publications Warehouse

    White, Amy C.; McKenzie, Stuart W.

    1979-01-01

    In 1978, data were collected for identification and quantification of benthic invertebrates, periphyton, and bottom material and their trace-metals concentrations from three sites in Salmon Creek basin, Wash. Metal analyses included arsenic, cadmium, chromium, copper, lead, zinc, selenium, and mercury. Physical data collected included water temperature, dissolved oxygen, pH, discharge, and size of cobbles and fine stream-bottom material. Additional chemical analyses included major constituents. Benthic invertebrate identifications were generally taken to the generic level, with a total of 49 taxons identified and quantified. A total of 36 periphyton taxons were quantified and identified, generally at the species level. (Woodard-USGS)

  10. Tertiary treatment of textile wastewater with combined media biological aerated filter (CMBAF) at different hydraulic loadings and dissolved oxygen concentrations.

    PubMed

    Liu, Fang; Zhao, Chao-Cheng; Zhao, Dong-Feng; Liu, Guo-Hua

    2008-12-15

    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 dissolved oxygen (DO) concentration, 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 concentrations, but this variation trend was not observed for TN removal. With the increase of DO concentrations 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%. PMID:18396373

  11. The effect of using different 0.45 μm filter membranes on 'dissolved' element concentrations in natural waters

    USGS Publications Warehouse

    Hall, G.E.M.; Bonham-Carter, G. F.; Horowitz, A.J.; Lum, K.; Lemieux, C.; Quemerais, B.; Garbarino, J.R.

    1996-01-01

    The effect of 4 different 0.45 ??m pore size filter membrane systems on the 'dissolved' concentration of 28 elements in 5 natural water samples of varying matrix is reported. In 3 of the 5 waters, consistently higher concentrations 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 concentration 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.

  12. Evaluating Function of a Constructed Fen in Alberta's Oil Sands Region Using Dissolved Organic Carbon Concentration and Chemistry

    NASA Astrophysics Data System (ADS)

    Strack, M.; Khadka, B.

    2014-12-01

    Peatlands, mainly fens, account for close to 65% of the landscape in the oil sands region near Fort McMurray, Alberta. Since mine closure plans require landscape reclamation, methods for fen construction are being investigated. As reclamation goals include the return of ecosystem function, criteria for evaluation must be developed. In this study we compare soil concentrations and spectrophometric properties of dissolved organic carbon (DOC) from a constructed fen during its first growing season with that collected from three diverse, undisturbed reference fens in the region. The constructed fen had lower DOC concentration than all the reference fens. Based on E2/E3, E4/E6 and specific UV absorbance of the DOC, the constructed fen had DOC with significantly greater humic content, aromatic nature, and larger molecular size than the reference fens. Results from laboratory DOC production studies indicate that these patterns are likely due to the limited DOC contribution from the newly planted vegetation at the constructed fen, resulting in DOC largely derived from humified peat placed during construction. These preliminary results suggest that DOC concentration and chemistry provide information about the ecological development of the constructed system that could be useful for evaluating reclamation success through time.

  13. Estimation of Concentration and Bonding Environment of Water Dissolved in Common Solvents Using Near Infrared Absorptivity

    PubMed Central

    Dickens, Brian; Dickens, Sabine H.

    1999-01-01

    Integrated near infrared (NIR) absorbance has been used to determine the absorptivity of the υ2 + υ3 combination band of the asymmetric stretch (υ2) and the bending vibration (υ3) for water in several organic solvents. Absorptivity measured in this way is essentially constant across the absorption envelope and is found to be 336 L mol−1 cm−1 with a standard deviation of 4 L mol−1 cm−1 as estimated from a least squares fit of a straight line to data from water concentrations between 0.01 mol/L and 0.06 mol/L. Absorptivity measured from the peak maximum of the υ2 + υ3 combination band of water varies with the type of hydrogen bonding of the water molecule because the shape of the NIR absorption envelope changes with the hydrogen bonding. Because the integrated NIR absorptivity of the υ2 + υ3 combination band of water is essentially constant across the absorption envelope, the NIR absorption envelope reflects the distribution of hydrogen bonding of the water. The shape and location of the absorption envelope appear to be governed mostly by the number of hydrogen bonds from the water molecules to easily polarized atoms. Water that is a donor in hydrogen bonds to atoms which are not easily polarized (such as the oxygen of a typical carbonyl group) absorbs near 5240 cm−1 to 5260 cm−1. Water that donates one hydrogen bond to an easily polarized atom (such as a water molecule oxygen) absorbs near 5130 cm−1 to 5175 cm−1, and water that donates two hydrogen bonds to easily polarized atoms is estimated to absorb near 5000 cm−1 to 5020 cm−1. Water donating two hydrogen bonds to other water molecules may be said to be in a water-like environment. In no case does a small amount of water absorbed in a host material appear to have a water-like environment.

  14. Estimation of Suspended and Dissolved Matter Concentration In Sea Water On Shelves By Satellite Remote Sensing

    NASA Astrophysics Data System (ADS)

    Pelevin, V.; Rostovtseva, V.

    Falling of rivers into the seas or surging in shallow aquatoria cause the violation of the balance between living and dead matter occurring in the open ocean ( Pelevin and Rostovtseva, 2001). That means in littoral arias the one-parameter model of sea waters optical properties developed for the open ocean (Pelevin and Rostovtseva, 1997) is not valid. We suggest to use the three-parameters model of light scattering and absorbing prop- erties of sea water for the most arias on shelves. The three parameters are: the coeffi- cient of light absorption by coloured matter at 500 nm (coloured matter includes both chlorophyll pigments and "yellow substance"), the coefficient of light absorption by suspended matter and the coefficient of light backscattering by suspended matter. For some specific shelf arias with coloured suspended matter we suggest to add the fourth parameter taking into account the spectral dependence of backscattering by suspended matter. The method of such type arias determination is also given. The algorithm of solution of the inverse problem of these parameters estimation using optical remote sensing data obtained from satellites is developed. It consists of two steps: the rough determination of the parameters values by some spectral characteris- tics and then the minimization of real and model spectra discrepancy. The suggested algorithm was used for spectral distribution of upward radiation mea- sured in the Black, Marmora and Baltic Seas. Comparison of the obtained results with some data of direct measurements carried out in these aquatoria proved the validity of the model for these shelf waters and showed the efficiency of the suggested approach. V.N.Pelevin and V.V.Rostovtseva , 1997, Estimation of lightscattering and lightabsorb- ing admixture concentration in open ocean waters of different types.- Atmospheric and Oceanic Optics, 10(9), 989-995. V.N.Pelevin and V.V.Rostovtseva, 2001, Modelling of optic- biological parameters of open ocean waters

  15. Dissolved Oxygen Concentration Profiles in the Hyporheic Zone Through the Use of a High-Density Fiber Optic Measurement Network

    NASA Astrophysics Data System (ADS)

    Reeder, William Jeffrey; Quick, Annika; Farrell, Tiffany B.; Benner, Shawn G.; Feris, Kevin P.; Tonina, Daniele

    2015-04-01

    The majority of chemical reactions in riverine systems occur within the hyporheic zone (HZ). Hyporheic exchange, flow into and out of the hyporheic zone, represents a primary control over those reactions because the flow rate will determine the residence time and amount of chemical constituents in the HZ. Hyporheic flow can be conceptualized as discreet streamlines that collectively represent a broad distribution of residence times. Within this context, dissolved oxygen (DO) concentration becomes a primary indicator of the redox and biochemical state of the HZ including, for example, the fate of carbon, contaminant behavior, nutrient cycling, stream DO levels and nitrous oxide (N2O) production. River systems have been identified as a significant source of N2O emissions, contributing an estimated 10% of anthropogenically generated N2O. The primary biochemical transformations that lead to N2O production are nitrification (NH4+ to NO3-) and denitrification (NO3- to N2) reactions that are mediated by microbes living in the HZ. Current theory describes a process in which DO enters the stoss side of the HZ and is consumed by respiration and nitrification in the upstream, oxic portion of the streamlines leading to a progressive partitioning of the HZ from oxic to anoxic. This conceptualization, however, has not been well validated in a physical sense, due to inherent difficulties associated with measuring chemical concentrations in the HZ. To test current theory, we measured HZ DO concentrations, in a large-scale flume experiment, almost continuously for five months using a multiplexed optical network and a precision robotic surface probe system. We were able to measure DO at higher spatial and temporal resolution than has been previously demonstrated. These measurements, coupled with detailed numerical modeling of HZ flowlines, allowed us to map HZ DO concentrations spatially and over time. Our findings validate the models that describe the consumption of DO through

  16. Heavy Metals Concentrations in Groundwater Used for Irrigation

    PubMed Central

    Taghipour, Hassan; Mosaferi, Mohammad; Pourakbar, Mojtaba; Armanfar, Feridoun

    2012-01-01

    Background: The main objective of this study was characterization of selected heavy metals concentrations (Lead, cadmium, copper, zinc, nickel and chromium) in groundwater used for ir-rigation in Tabriz City's countryside. Methods: After consulting with the experts of agriculture department and site survey, 38 irriga-tion water samples were taken from different farms (34 wells) without primary coordination with farm owners. All of samples were acidified to achieve pH≈2 and then were concentrated from 10 to 1 volume. The concentrations of Cd, Pb, Cu, Cr, Ni, and Zn in the samples (totally 228) were determined with a flame atomic absorption spectrophotometer. Results: In none of 38 farms, irrigation with surface runoff and industrial wastewater was ob-served. The average concentrations of Cd, Pb, Cu, Cr, Ni, and Zn in the irrigated water were de¬termined 6.55, 0.79, 16.23, 3.41, 4.49, and 49.33µg/L, respectively. The average and even maxi¬mum concentrations of heavy metals in the irrigation water at the studied area were less than toxicity threshold limits of agricultural water. Conclusion: Currently, not using of surface runoff and industrial wastewater as irrigation water by farmers indicates that the controlling efforts by authorities have been effective in the area. Water used for irrigation of the farms and groundwater of the studied area are not polluted with heavy metals and there is no risk from this viewpoint in the region. PMID:24688935

  17. Heavy metal and radionuclide concentrations in fly ash material

    SciTech Connect

    Booker, J.D.; Phagan, C.J.; Gray, R.H.

    1995-12-31

    A study was completed to characterize the concentrations of heavy metals and radionuclides and their mobility in two fly ash covered parking lots at the US Department of Energy`s Pantex Plant. Six composite samples collected from the parking areas were analyzed by an offsite contract laboratory for arsenic, barium, cadmium, chromium, lead, mercury, selenium, silver, uranium 234, and uranium 238. All metal and radionuclide concentrations except mercury and silver exceeded the applicable comparison standards for typical Pantex Plant soil; however, concentrations of mercury and silver were significantly below the Texas Risk Reduction Standards. In view of these results, it was strongly recommended that fly ash not be used for future projects at the Pantex Plant unless specialized engineering controls are used.

  18. Seasonal Control of Surface-Water Dissolved Iron Concentrations by Suspended Particle Concentrations on the Northern Gulf of Alaska Continental Shelf and Slope

    NASA Astrophysics Data System (ADS)

    Crusius, J.; Schroth, A. W.; Campbell, R.; Cullen, J. T.; Dillman, D.; Resing, J.

    2012-12-01

    The continental shelf region of the northern Gulf of Alaska (GoA) supports a productive ecosystem including an important commercial fishery. Downwelling winds during most of the year imply that some mechanism other than upwelling must be supplying the essential nutrients iron and nitrate. Although it is well known that iron limits productivity offshore in the GoA, we have a poor understanding of the controls on Fe supply. Data from cruises from 2010 provide some new insight into the mechanisms of Fe supply. Cruises were carried out along a transect extending from the mouth of the Copper River to ~40 km beyond the shelf break three times per year including early April, early May, and late July. High-resolution surface-water sampling was carried out, as well as bottle casts at 5 stations. High, fairly uniform concentrations of "total dissolvable iron" (TDFe; unfiltered sample acidified to pH=1.7) as well as "dissolved" Fe (dFe) were observed spanning the shelf in April, suggesting sediment resuspension is an important source of dFe to surface waters at that time. By contrast, high dFe and TDFe concentrations in late July coincide with low-salinity surface water, which in this location indicates a glacial meltwater source. Throughout spring and summer high particle concentrations across much of the shelf appear to "buffer" dFe concentrations to ~3 nmol/kg, which are close to those observed by Lippiatt et al (2010) in the region. This is consistent with dFe concentrations being determined by the organic ligand concentrations that, in turn, are fairly constant. In late July, surface water dFe concentrations are ~0.5 nmol/kg on the outer shelf and up to ~50 km further offshore. These dFe concentrations on the outer shelf are much lower in July than earlier in the year, owing to Fe removal by phytoplankton uptake and by scavenging, as well as by the lack of particulate Fe sources to surface waters in July. However, the high surface-water dFe observed ~50 km beyond the

  19. Evaluation of the Chemcatcher and DGT passive samplers for monitoring metals with highly fluctuating water concentrations.

    PubMed

    Allan, Ian J; Knutsson, Jesper; Guigues, Nathalie; Mills, Graham A; Fouillac, Anne-Marie; Greenwood, Richard

    2007-07-01

    ) that associate to a significant degree with suspended solids, colloids or dissolved organic carbon, or form complexes with large organic ligands, optimum agreement was with the filtered or ultrafiltered fractions and with the predicted inorganic and inorganic-fulvic acid associated fractions. While Chemcatcher-based TWA concentration ranges for Cu and Zn were in best agreement with the total filtered fraction, there was lack of agreement for Pb. The combined use of DGT devices with open pore (OP) and restricted pore (RP) gels allowed the labile fraction of metal associated with large organic ligands or DOC to be differentiated and quantified, since this is available to DGT OP but unable to diffuse into the DGT RP. This evaluation of the two sampling devices clearly demonstrated their ability to react reliably to transient peaks in concentration of metal pollutants in water and indicated where future efforts are needed to improve calibration data. Such samplers may prove valuable in responding to the monitoring requirements of the European Union's Water Framework Directive. PMID:17607387

  20. Influence of acid volatile sulfides and metal concentrations on metal partitioning in contaminated sediments

    USGS Publications Warehouse

    Lee, J.-S.; Lee, B.-G.; Luoma, S.N.; Choi, H.J.; Koh, C.-H.; Brown, C.L.

    2000-01-01

    The influence of acid volatile sulfide (AVS) on the partitioning of Cd, Ni, and Zn in porewater (PW) and sediment as reactive metals (SEM, simultaneously extracted metals) was investigated in laboratory microcosms. Two spiking procedures were compared, and the effects of vertical geochemical gradients and infaunal activity were evaluated. Sediments were spiked with a Cd-Ni-Zn mixture (0.06, 3, 7.5 ??mol/g, respectively) containing four levels of AVS (0.5, 7.5, 15, 35 ??mol/g). The results were compared to sediments spiked with four levels of Cd-Ni-Zn mixtures at one AVS concentration (7.5 ??mol/g). A vertical redox gradient was generated in each treatment by an 18-d incubation with an oxidized water column. [AVS] in the surface sediments decreased by 65-95% due to oxidation during incubation; initial [AVS] was maintained at 0.5-7.5 cm depth. PW metal concentrations were correlated with [SEM - AVS] among all data. But PW metal concentrations were variable, causing the distribution coefficient, Kd(pw) (the ratio of [SEM] to PW metal concentrations) to vary by 2-3 orders of magnitude at a given [SEM - AVS]. One reason for the variability was that vertical profiles in PW metal concentrations appeared to be influenced by diffusion as well as [SEM - AVS]. The presence of animals appeared to enhance the diffusion of at least Zn. The generalization that PW metal concentrations are controlled by [SEM - AVS] is subject to some important qualifications if vertical gradients are complicated, metal concentrations vary, or equilibration times differ.The influence of acid volatile sulfide (AVS) on the partitioning of Cd, Ni, and Zn in porewater (PW) and sediment as reactive metals (SEM, simultaneously extracted metals) was investigated in laboratory microcosms. Two spiking procedures were compared, and the effects of vertical geochemical gradients and infaunal activity were evaluated. Sediments were spiked with a Cd-Ni-Zn mixture (0.06, 3, 7.5 ??mol/g, respectively) containing

  1. An Isotope Dilution Method for High-frequency Measurements of Dissolved Inorganic Carbon concentration in the Surface Ocean

    NASA Astrophysics Data System (ADS)

    Huang, K.; Bender, M. L.; Wanninkhof, R. H.; Cassar, N.

    2013-12-01

    Dissolved inorganic carbon (DIC) is one of the most important species in the ocean carbon system. An autonomous system using isotope dilution as its core method has been developed to obtain high-frequency measurements of dissolved inorganic carbon (DIC) concentrations in the surface ocean. This system accurately mixes a seawater sample and a 13C-labeled sodium bicarbonate solution (spike). The mixed solution is then acidified and sent through a gas permeable membrane contactor. CO2 derived from DIC in the mixture is extracted by a CO2-free gas stream, and is sent to a cavity ring-down spectrometer to analyze its 13C/12C ratio. [DIC] of the seawater can then be derived from the measured 13C/12C, the known mixing ratio and the [DI13C] of the spike. The method has been tested under a wide [DIC] range (1800-2800 μmol/kg) in the laboratory. It has also been deployed on a cruise that surveyed ocean waters to the south of Florida. At a sampling resolution of 4 minutes (15 samples per hour), the relative standard deviation of DIC determined from the laboratory tests and the field deployment is ×0.07% and ×0.09%, respectively. The accuracy of the method is better than 0.1% except where [DIC] varies faster than 5 μmol/kg per minute. Based on the laboratory and field evaluations, we conclude that this method can provide accurate underway [DIC] measurements at high resolution in most oceanic regions. Schematic illustration of the work flow.

  2. Effect of pH, ionic strength, dissolved organic carbon, time, and particle size on metals release from mine drainage impacted streambed sediments.

    PubMed

    Butler, Barbara A

    2009-03-01

    Acid-mine drainage (AMD) input to a stream typically results in the stream having a reduced pH, increased concentrations of metals and salts, and decreased biological productivity. Removal and/or treatment of these AMD sources is desired to return the impacted stream(s) to initial conditions, or at least to conditions suitable for restoration of the aquatic ecosystem. Some expected changes in the water chemistry of the stream following removal of AMD input include an increase in pH, a decrease in ionic strength, and an increase in dissolved organic carbon (DOC) concentrations from increased biological activity in the absence of toxic metals concentrations. These changes in water chemistry may cause the existing contaminated bed sediments to become a source of metals to the stream water. Streambed sediments, collected from North Fork Clear Creek (NFCC), Colorado, currently impacted by AMD, were assessed for the effects of pH, ionic strength, DOC concentration, time, and particle size on metals release using a factorial design. The design included two levels for each chemical parameter (ionic strength = 40 and 80% lower than ambient; pH = 6 and 8; and DOC = 1 and 3 mg/l higher than ambient), ten sampling times (from zero to 48 h), and two size fractions of sediments (63 microm < or = x < 2 mm and < 63 microm). Greater concentrations of metals were released from the smaller sized sediments compared with the larger, with the exception of Cu. A mild acid digestion (0.6M HCl) evaluated the amount of each metal that could be removed easily from each of the sediment size fractions. Release of all metals over all time points, treatments, and from both sediment sizes was less than 1% of the extractable concentrations, with the exception of Mn, which ranged from 4 to 7% from the smaller sized sediment. Greater percentages of the 0.6M HCl-extractable concentrations of Cu, Fe, and Zn were released from the larger sized sediment, while this was true for release of Cd and Mn from

  3. Concentrations and fluxes of dissolved organic carbon in runoff from a forested catchment: insights from high frequency measurements

    NASA Astrophysics Data System (ADS)

    Strohmeier, S.; Knorr, K.-H.; Reichert, M.; Frei, S.; Fleckenstein, J. H.; Peiffer, S.; Matzner, E.

    2012-08-01

    Concentrations of dissolved organic carbon (DOC) in runoff from catchments are often subject to substantial short term variations. The aim of this study was to identify the spatial sources of DOC and the causes for short term variations in runoff from a forested catchment. Furthermore, we investigated the implication of short term variations for the calculation of annual runoff fluxes. High frequency measurements (30 min intervals) of DOC in runoff, of discharge and groundwater table were conducted for one year in the 4.2 km2 forested Lehstenbach catchment, Germany. Riparian wetland soils represent about 30% of the catchment area. The quality of DOC was investigated by three dimensional fluorescence excitation-emission matrices in samples taken from runoff, deep groundwater and shallow groundwater from the riparian wetland soils. The concentrations of DOC in runoff were highly variable at an hourly to daily time scale, ranging from 2.6 mg l-1 to 34 mg l-1 with an annual average of 9.2 mg l-1. The concentrations were positively related to discharge, with a pronounced, counter clockwise hysteresis. Relations of DOC to discharge were steeper in the summer/fall than in the winter/spring season. Dynamics of groundwater table, discharge, DOC concentrations and DOC quality parameters indicated that DOC in runoff originated mainly from the riparian wetland soils, both under low and high flow conditions. The annual export of DOC from the catchment was 84 kg C ha-1 yr-1 when calculated from the high frequency measurements. If the annual export was calculated by simulated random fortnightly samplings, the range was 47 to 124 kg C ha-1 yr-1. Calculations of DOC export fluxes might result in significant errors when based on infrequent (e.g. fortnightly) sampling intervals. Future changes in the precipitation and discharge patterns will influence the DOC dynamics in this catchment, with largest effects in the summer season.

  4. Concentrations and fluxes of dissolved organic carbon in runoff from a forested catchment: insights from high frequency measurements

    NASA Astrophysics Data System (ADS)

    Strohmeier, S.; Knorr, K.-H.; Reichert, M.; Frei, S.; Fleckenstein, J. H.; Peiffer, S.; Matzner, E.

    2013-02-01

    Concentrations of dissolved organic carbon (DOC) in runoff from catchments are often subject to substantial short-term variations. The aim of this study was to identify the compartmental sources of DOC in a forested catchment and the causes for short-term variations in runoff. Furthermore, we investigated the implication of short-term variations for the calculation of annual runoff fluxes. High frequency measurements (30 min intervals) of DOC in runoff, of discharge and groundwater table were conducted for one year in the 4.2 km2 forested Lehstenbach catchment, Germany. Riparian wetland soils represent about 30% of the catchment area. The quality of DOC was investigated by three dimensional fluorescence excitation-emission matrices in samples taken from runoff, deep groundwater and shallow groundwater from the riparian wetland soils. The concentrations of DOC in runoff were highly variable at an hourly to daily time scale, ranging from 2.6 mg L-1 to 34 mg L-1 with an annual average of 9.2 mg L-1. The concentrations were positively related to discharge, with a counter clockwise hysteresis. Relations of DOC to discharge were steeper and the degree of hysteresis larger in the summer/fall than in the winter/spring period. Dynamics of groundwater table, discharge, DOC concentrations and DOC quality parameters indicated that DOC in runoff originated mainly from the riparian wetland soils, both under low and high flow conditions. The annual export of DOC from the catchment was 84 kg C ha-1 yr-1 when calculated from the high frequency measurements. If the annual export was calculated by simulated samplings of >2 days intervals substantial deviations resulted. Predicted changes in precipitation and discharge patterns as well as generally increasing temperatures likely will cause raising DOC exports from this catchment.

  5. Effects of dissolved organic matter (DOM) at environmentally relevant carbon concentrations on atrazine degradation by Chelatobacter heintzii SalB.

    PubMed

    Cheyns, Karlien; Calcoen, Jasper; Martin-Laurent, Fabrice; Bru, David; Smolders, Erik; Springael, Dirk

    2012-09-01

    The dissolved organic matter (DOM) is the term used for organic components of natural origin present in the soil solution and is probably the most available C-source that primes microbial activity in subsoils. Contrasting effects of organic C components on pesticide degradation have been reported; however, most studies have used model organic compounds with compositions and concentrations which differ substantially from those found in the environment. Degradation of atrazine (AT) by Chelatobacter heintzii SalB was monitored in liquid batch assays in the absence or presence of well-defined model C compounds (glucose, gluconate and citrate) as model DOM (mDOM) or complex, less-defined, environmental DOM solutions (eDOM: isolated humic substances, soil and plant residue extracts) at environmentally relevant concentrations. Glucose significantly increased AT degradation rate by more than a factor of 8 at and above 2.5 mg C L( - 1). Optical density measurements showed that this stimulation is related to microbial growth. Gluconate and citrate had no effects unless at non-relevant concentrations (1,000 mg DOC L( - 1)) at which stimulations (gluconate) or inhibitions (citrate) were found. The effects of eDOM added at 10 mg DOC L( - 1) on AT degradation were generally small. The AT degradation time was reduced by factors 1.4-1.9 in the presence of humic acids and eDOM from soils amended with plant residues; however, no effects were found for fulvic acids or eDOM from a soil leachate solution or extracted from unamended peat or forest soil. In conclusion, DOM supplied as both mDOM and eDOM did not inhibit AT degradation at environmentally relevant concentrations, and stimulation can be found for selected DOM samples and this is partly related to its effect on growth. PMID:22159734

  6. Binding of mercury(II) to dissolved organic matter: The role of the mercury-to-DOM concentration ratio

    USGS Publications Warehouse

    Haitzer, M.; Aiken, G.R.; Ryan, J.N.

    2002-01-01

    The binding of Hg(II) to dissolved organic matter (DOM; hydrophobic acids isolated from the Florida Everglades by XAD-8 resin) was measured at a wide range of Hg-to-DOM concentration ratios using an equilibrium dialysis ligand exchange method. Conditional distribution coefficients (KDOM???) determined by this method were strongly affected by the Hg/DOM concentration ratio. At Hg/DOM ratios below approximately 1 ??g of Hg/mg of DOM, we observed very strong interactions (KDOM??? = 1023.2??1.0 L kg-1 at pH = 7.0 and I = 0.1), indicative of mercury-thiol bonds. Hg/DOM ratios above approximately 10 ??g of Hg/mg of DOM, as used in most studies that have determined Hg-DOM binding constants, gave much lower KDOM??? values (1010.7??1.0 L kg-1 at pH = 4.9-5.6 and I = 0.1), consistent with Hg binding mainly to oxygen functional groups. These results suggest that the binding of Hg to DOM under natural conditions (very low Hg/DOM ratios) is controlled by a small fraction of DOM molecules containing a reactive thiol functional group. Therefore, Hg/DOM distribution coefficients used for modeling the biogeochemical behavior of Hg in natural systems need to be determined at low Hg/DOM ratios.

  7. Modeling hourly dissolved oxygen concentration (DO) using two different adaptive neuro-fuzzy inference systems (ANFIS): a comparative study.

    PubMed

    Heddam, Salim

    2014-01-01

    This article presents a comparison of two adaptive neuro-fuzzy inference systems (ANFIS)-based neuro-fuzzy models applied for modeling dissolved oxygen (DO) concentration. The two models are developed using experimental data collected from the bottom (USGS station no: 420615121533601) and top (USGS station no: 420615121533600) stations at Klamath River at site KRS12a nr Rock Quarry, Oregon, USA. The input variables used for the ANFIS models are water pH, temperature, specific conductance, and sensor depth. Two ANFIS-based neuro-fuzzy systems are presented. The two neuro-fuzzy systems are: (1) grid partition-based fuzzy inference system, named ANFIS_GRID, and (2) subtractive-clustering-based fuzzy inference system, named ANFIS_SUB. In both models, 60 % of the data set was randomly assigned to the training set, 20 % to the validation set, and 20 % to the test set. The ANFIS results are compared with multiple linear regression models. The system proposed in this paper shows a novelty approach with regard to the usage of ANFIS models for DO concentration modeling. PMID:24057665

  8. Increased Hepatitis B surface antigen production by recombinant Aspergillus niger through the optimization of agitation and dissolved oxygen concentration.

    PubMed

    James, Emmanuel R; van Zyl, Willem H; Görgens, Johann F

    2007-05-01

    The capacity of the filamentous fungi Aspergillus niger to produce and assemble complex immunogenic viral proteins into virus-like particles (VLPs) in batch culture was enhanced by optimizing the bioprocessing parameters, agitation intensity and dissolved oxygen (dO(2)) concentration. Response surface methodology (RSM) and a two-factor-two-level central composite rotatable design (CCRD) were employed to evaluate the interactive response pattern between parameters and their optimum combination. The recombinant hepatitis B surface antigen (HBsAg) was used as a model VLP system to determine the effect of these parameters on biomass yield, fungal morphology, HBsAg production and bioreactor kinetics. The response surface model predicted optimum cultivation conditions at an agitation of rate of 100 rpm and a dO(2) concentration of 25%, obtaining highest intracellular membrane-associated HBsAg levels of [see text]. HBsAg production levels were increased tenfold compared to yields obtained in shake flask cultivation. Although hepatitis B VLPs mostly accumulated intracellularly, optimal bioreactor conditions resulted in significant HBsAg release in culture supernatant. These results compare favourably with other recombinant VLP systems in batch culture, and therefore, indicate a substantial potential for further engineering of the A. niger production system for the high level of intracellular and extracellular VLP production. PMID:17308907

  9. 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. PMID:26039657

  10. Nitrogen removal from wastewater and bacterial diversity in activated sludge at different COD/N ratios and dissolved oxygen concentrations.

    PubMed

    Zielińska, Magdalena; Bernat, Katarzyna; Cydzik-Kwiatkowska, Agnieszka; Sobolewska, Joanna; Wojnowska-Baryła, Irena

    2012-01-01

    The impact of the organic carbon to nitrogen ratio (chemical oxygen demand (COD)/N) in wastewater and dissolved oxygen (DO) concentration 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 concentration. Amplicons with sequences indicating membership of the genus Nitrosospira were the determinants of variable technological conditions. PMID:23505865

  11. Determination of size‐dependent metal distribution in dissolved organic matter by SEC‐UV/VIS‐ICP‐MS with special focus on changes in seawater

    PubMed Central

    Rathgeb, Anna; Causon, Tim; Krachler, Regina

    2016-01-01

    Iron is an essential micronutrient for all marine organisms, but it is also a growth limiting factor as the iron concentrations in the open ocean are below 1 nmol/L in sea water iron is almost entirely bound to organic ligands of the dissolved organic matter fraction, which are mostly of unknown structure. The input from rivers was traditionally considered as less important due to estuarine sedimentation processes of the mainly colloidal iron particles. However, recent studies have shown that this removal is not complete and riverine input may represent an important iron source in the open ocean. In this context, iron transport by land‐derived natural organic matter (NOM), and dissolved organic matter (DOM) have been identified as carrier mechanisms for riverine iron. The aim of this work is to characterize complexes containing iron and other metals in waters simulating estuarine conditions in order to help understand which role iron‐DOM compounds play in the open ocean. A method based on size‐exclusion chromatography (SEC) with sequential UV/VIS and ICP‐MS detection was developed for investigation of DOM size distribution and for assessment of the size‐dependent metal distribution in NOM‐rich surface water. Furthermore, sample matrix experiments were also performed revealing a dependence of DOM size distribution upon seawater concentration and different compounds present in seawater. Finally, efforts toward determination of DOM size with standardization with typical SEC standards indicate that only relative comparisons are possible with this approach, and that the sample matrix composition strongly influences obtained results. PMID:26814136

  12. Determination of size-dependent metal distribution in dissolved organic matter by SEC-UV/VIS-ICP-MS with special focus on changes in seawater.

    PubMed

    Rathgeb, Anna; Causon, Tim; Krachler, Regina; Hann, Stephan

    2016-04-01

    Iron is an essential micronutrient for all marine organisms, but it is also a growth limiting factor as the iron concentrations in the open ocean are below 1 nmol/L in sea water iron is almost entirely bound to organic ligands of the dissolved organic matter fraction, which are mostly of unknown structure. The input from rivers was traditionally considered as less important due to estuarine sedimentation processes of the mainly colloidal iron particles. However, recent studies have shown that this removal is not complete and riverine input may represent an important iron source in the open ocean. In this context, iron transport by land-derived natural organic matter (NOM), and dissolved organic matter (DOM) have been identified as carrier mechanisms for riverine iron. The aim of this work is to characterize complexes containing iron and other metals in waters simulating estuarine conditions in order to help understand which role iron-DOM compounds play in the open ocean. A method based on size-exclusion chromatography (SEC) with sequential UV/VIS and ICP-MS detection was developed for investigation of DOM size distribution and for assessment of the size-dependent metal distribution in NOM-rich surface water. Furthermore, sample matrix experiments were also performed revealing a dependence of DOM size distribution upon seawater concentration and different compounds present in seawater. Finally, efforts toward determination of DOM size with standardization with typical SEC standards indicate that only relative comparisons are possible with this approach, and that the sample matrix composition strongly influences obtained results. PMID:26814136

  13. +2 Valence Metal Concentrations in Lion Creek, Oakland, California

    NASA Astrophysics Data System (ADS)

    Vazquez, P.; Zedd, T.; Chagolla, R.; Dutton-Starbuck, M.; Negrete, A.; Jinham, M.; Lapota, M.

    2012-12-01

    Seven major creeks exist within the City of Oakland, California. These creeks all flow in the southwest direction from forested hills down through densely populated streets where they become susceptible to urban runoff. Lion Creek has been diverted to engineered channels and underground culverts and runs directly under our school (Roots International) before flowing into the San Leandro Bay. One branch of the creek begins near an abandoned sulfur mine. Previous studies have shown that extremely high levels of lead, arsenic and iron exist in this portion of the creek due to acid mine drainage. In this study +2 valence heavy metals concentration data was obtained from samples collected from a segment of the creek located approximately 2.8 miles downstream from the mine. Concentrations in samples collected at three different sites along this segment ranged between 50 ppb and 100 ppb. We hypothesize that these levels are related to the high concentration of +2 valence heavy metals at the mining site. To test this hypothesis, we have obtained samples from various locations along the roughly 3.75 miles of Lion Creek that are used to assess changes in heavy metals concentration levels from the mining site to the San Leandro Bay.

  14. Hydroclimatic Controls on the Seasonal and Inter-Annual Variability of Dissolved Phosphorus Concentration in a Lowland Agricultural Catchment

    NASA Astrophysics Data System (ADS)

    Dupas, R.; Gascuel-odoux, C.; Grimaldi, C.; Gruau, G.

    2014-12-01

    We investigated soluble reactive phosphorus (SRP) at the outlet of a lowland agricultural catchment (Kervidy-Naizin, France) to identify the hydroclimatic controls on the seasonal and inter-annual variability in concentrations. Six years of stream data have been used, including a regular 6-daily sampling and high-frequency monitoring of 52 floods. Both on an annual basis and during flood events, distinct export dynamics for SRP and particulate phosphorus (PP) revealed that SRP transport mechanism was independent from PP (Dupas et al., submitted). During most flood events, discharge-SRP hystereses were anticlockwise, which suggests that SRP was transferred to the stream via subsurface flow. Groundwater rise in wetland soils was likely the cause of this transfer, through the hydrological connectivity it created between the stream and P-rich soil horizons. SRP concentrations were highest in the beginning of the hydrological year (period A), when the stream started to flow again after the dry summer season and water table fluctuated in the wetland domain. Thus, wetland soils seemed to be a major source of SRP. Concentrations during period A were higher after a long summer period than after a short one, which suggest that a pool of labile P was constituted in soils during the dry summer period. During winter (period B), SRP concentration generally decreased compared to period A, both during floods and interflood. This could be due to depletion of a soil P pool in the wetland domain and/or dilution by deep groundwater with low P concentration from the upland domain. Concentration during period B barely decreased compared to A during wet years, probably due to increased connectivity with soils from the upland domain in wet conditions. During spring (period C), SRP concentration increased during baseflow periods. The possible mechanisms causing the release of SRP could involve reduction of Fe oxide-hydroxides in wetland soils or in-stream processes. At the same time, SRP

  15. 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. PMID:26319635

  16. A simple dissolved metals mixing method to produce high-purity MgTiO{sub 3} nanocrystals

    SciTech Connect

    Pratapa, Suminar E-mail: suminar-pratapa@physics.its.ac.id; Baqiya, Malik A. E-mail: suminar-pratapa@physics.its.ac.id; Istianah, E-mail: suminar-pratapa@physics.its.ac.id; Lestari, Rina E-mail: suminar-pratapa@physics.its.ac.id; Angela, Riyan E-mail: suminar-pratapa@physics.its.ac.id

    2014-02-24

    A simple dissolved metals mixing method has been effectively used to produce high-purity MgTiO{sub 3} (MT) nanocrystals. The method involves the mixing of independently dissolved magnesium and titanium metal powders in hydrochloric acid followed by calcination. The phase purity and nanocrystallinity were determined by making use of laboratory x-ray diffraction data, to which Rietveld-based analyses were performed. Results showed that the method yielded only one type magnesium titanate powders, i.e. MgTiO{sub 3}, with no Mg{sub 2}TiO{sub 4} or MgTi{sub 2}O{sub 5} phases. The presence of residual rutile or periclase was controlled by adding excessive Mg up to 5% (mol) in the stoichiometric mixing. The method also resulted in MT nanocrystals with estimated average crystallite size of 76±2 nm after calcination at 600°C and 150±4 nm (at 800°C). A transmission electron micrograph confirmed the formation of the nanocrystallites.

  17. Metal hydrides for concentrating solar thermal power energy storage

    NASA Astrophysics Data System (ADS)

    Sheppard, D. A.; Paskevicius, M.; Humphries, T. D.; Felderhoff, M.; Capurso, G.; Bellosta von Colbe, J.; Dornheim, M.; Klassen, T.; Ward, P. A.; Teprovich, J. A.; Corgnale, C.; Zidan, R.; Grant, D. M.; Buckley, C. E.

    2016-04-01

    The development of alternative methods for thermal energy storage is important for improving the efficiency and decreasing the cost of concentrating solar thermal power. We focus on the underlying technology that allows metal hydrides to function as thermal energy storage (TES) systems and highlight the current state-of-the-art materials that can operate at temperatures as low as room temperature and as high as 1100 °C. The potential of metal hydrides for thermal storage is explored, while current knowledge gaps about hydride properties, such as hydride thermodynamics, intrinsic kinetics and cyclic stability, are identified. The engineering challenges associated with utilising metal hydrides for high-temperature TES are also addressed.

  18. Correlation between the limiting pH of metal ion solubility and total metal concentration

    SciTech Connect

    Apak, R.; Hizal, J.; Ustaer, C.

    1999-03-15

    As an alternative to species distribution diagrams (pM vs pH curves in aqueous solution) drawn for a fixed total metal concentration, this work has developed simple linear models for correlating the limiting pH of metal ion solubility -- in equilibrium with the least soluble amorphous metal hydroxide solid phase -- to the total metal concentration. Thus adsorptive metal removal processes in complex systems can be better designed once the limiting pH of heavy metal solubility (i.e., pH{sup *}) in such a complex environment can be envisaged by simple linear equations. pH{sup *} vs pM{sub t} (M{sub t} = total metal concentration that can exist in aqueous solution in equilibrium with M(OH){sub 2(s)}) linear curves for uranyl-hydroxide, uranyl-carbonate-hydroxide, and mercuric-chloride-hydroxide simple and mixed-ligand systems and cupric-carbonate-hydroxide complexes in equilibrium with mixed hydroxide solid phases may enable the experimental chemist to distinguish true adsorption (e.g., onto hydrous oxide sorbents) from bulk precipitation removal of the metal and to interpret some anomalous metal fixation data -- usually attributed to pure adsorption in the literature -- with precipitation if the pM{sub t} at the studied pH is lower than that tolerated by pH{sup *} vs pM{sub t} curves. This easily predictable pH{sup *} corresponding to a given pM{sub t} may aid the design of desorptive mobilization experiments for certain metals as well as their adsorptive removal with the purpose of simulating metal adsorption and desorption cycles in real complex environments with changing groundwater pH.

  19. Influence of increasing dissolved inorganic carbon concentrations and decreasing pH on chemolithoautrophic bacteria from oxic-sulfidic interfaces

    NASA Astrophysics Data System (ADS)

    Mammitzsch, K.; Jost, G.; Jürgens, K.

    2012-12-01

    Increases in the dissolved inorganic carbon (DIC) concentration are expected to cause a decrease in the pH of ocean waters, a process known as ocean acidification. In oxygen-deficient zones this will add to already increased DIC and decreased pH values. It is not known how this might affect microbial communities and microbially mediated processes. In this study, the potential effects of ocean acidification on chemolithoautotrophic prokaryotes of marine oxic-anoxic transition zones were investigated, using the chemoautotrophic denitrifying ɛ-proteobacterium "Sulfurimonas gotlandica" strain GD1 as a model organism. This and related taxa use reduced sulfur compounds, e.g. sulfide and thiosulfate, as electron donors and were previously shown to be responsible for nitrate removal and sulfide detoxification in redox zones of the Baltic Sea water column but occur also in other oxygen-deficient marine systems. Bacterial cell growth within a broad range of DIC concentrations and pH values was monitored and substrate utilization was determined. The results showed that the DIC saturation concentration for growth was already reached at 800 μM, which is well below in situ DIC levels. The pH optimum was between 6.6 and 8.0. Within a pH range of 6.6-7.1 there was no significant difference in substrate utilization; however, at lower pH values cell growth decreased sharply and cell-specific substrate consumption increased. These findings suggest that a direct effect of ocean acidification, with the predicted changes in pH and DIC, on chemolithoautotrophic bacteria such as "S. gotlandica" str. GD1 is generally not very probable.

  20. Concentration and partitioning of metals in intertidal biofilms: implications for metal bioavailability to shorebirds.

    PubMed

    McCormick, Jodine; St Clair, C Toby; Bendell, L I

    2014-03-01

    We compared zinc, copper and cadmium concentrations and the operationally defined geochemical partitioning of the three metals in sediments enriched with biofilm versus sediments without obvious biofilm present (reference) sampled from five locations within the Fraser River Delta, British Columbia, Canada. Two-way ANOVA's with site and biofilm (enriched or reference) as the two factors were applied to determine if metal concentrations or the partitioning of the metal was dependent on the two factors. Sediment enriched in biofilm contained greater amounts of aqua regia extracted zinc and copper and tended to have greater amounts of reducible cadmium as compared to reference sediments. By contrast, reference sediments had greater concentrations of easily reducible copper suggesting differences in speciation between the two sediment types. Greater concentrations of reducible cadmium within biofilm may provide a route of contaminant exposure to shorebirds whose diet is dependent on biofilm. PMID:24381098

  1. Heavy metal concentrations in water, suspended matter, and sediment from Gökova Bay, Turkey.

    PubMed

    Balkis, Nuray; Aksu, Abdullah; Okuş, Erdoğan; Apak, Reşat

    2010-08-01

    The contents of heavy metals (Fe, Mn, Pb, Cu, Cd, and Hg) dissolved in water and suspended solids of Gökova Bay--partly and fully sampled in 2005 and 2006, respectively--are quite higher than the average values encountered in uncontaminated sea water. The high concentrations are associated with terrestrial inputs from the mining zones and anthropogenic (domestic+industrial) sources. Moreover, the distribution of Fe and Cu is affected by primary production because these elements function as nutrients in biological activities. The Cr, Ni, and Fe concentrations of surface sediments are above the shale average. The Cr and Ni contents of surface sediments representative of river mouths strongly correlate with total phosphorus contents. In a sulfide-poor environment, Pb and Cu were concentrated at a higher ratio in surface sediments than Cd, probably due to higher stabilities of their surface complexes with amorphous iron oxides and clay minerals existing as major components in the sediments. The exceptional enrichment of Zn may be attributed to double oxide formation with amorphous iron oxides in sediments. The high metal values are most probably caused by terrestrial inputs from anthropogenic sources and the mining zones at the southeast part of the bay. The Al, Mn, Pb, Cu, Zn, and Hg contents are below the shale average. The low values have possibly originated from the coarse-grained sandy sediments having a low affinity for metals. There are no distinct differences in the metal distributions in water and suspended matter between the years 2005 and 2006 in the bay, probably due to low sedimentation rates. PMID:19565345

  2. Water quality in the Fort Cobb Watershed, USA: Spatial and temporal patterns of dissolved P stream concentrations

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Dissolved phosphorus (P) has often been identified as the nutrient of concern in lakes, reservoirs and streams especially where there is evidence of eutrophication. The objective of this work is to identify spatial and temporal patterns in dissolved P [soluble reactive P (SRP) and bioavailable P (B...

  3. Concentrations and chemical forms of trace metals in coastal seawater on coral reef and their seasonal variation

    NASA Astrophysics Data System (ADS)

    Ganaha, S.; ITOH, A.

    2011-12-01

    Coastal seawater on coral reef near Okinawa island in Japan, which is in oligotrophic condition, has a diverse and unique ecosystem. It is possible that nutritive sals and trace metals, classified into nutrient type, are effectively supplied to marine phytoplankton and zooxanthellae from seawater. However, the concentrations and chemical forms of trace metals in coastal seawater on coral reef have been scarcely reported so far. In the present study, the characteristics of the concentrations and chemical forms of trace metals in such a seawater were investigated with seasonal variation by analyzing the coastal seawater at every month, after an analytical method for a simple chemical speciation including on-site treatment was established. The analytical method using a chelating resin and a disposable syringe was employed for de-salt and preconcentration of trace metals in costal seawater. After that, trace metals in the concentrated solution were measured by ICP-MS. Three types of chemical forms of an ionic, a dissolved, and an acid-soluble were separated without any treatment, by filtering with membrane filter of 0.45 μm, and by filtering after adding nitric acid, respectively. Then, a monitoring investigation of the coastal seawater on coral reef, located at Sesoko island near the northern part of Okinawa island, was carried out once at every month from Sep. 2010 to Aug. 2011. As a result, 10 elements in the dissolved form in each sample could be determined. The average concentrations for all samples from Sep. 2010 to Apr. 2011 were as follows: Mo:10.7 ppb, U:3.2 ppb, V:1.5 ppb, Mn:0.17 ppb, Ni:0.16 ppb, Zn:0.13 ppb, Cu:0.070 ppb, Pb:0.024 ppb, Co:0.0022 ppb, Cd:0.0016ppb. The concentrations for most trace metals were almost close to ones in open surface seawater of the Pacific ocean. For the acid-soluble form, the concentrations of V, Mo, and U were almost same with those of the dissolved form, and ones of Mn, Co, Ni, Cu, and Cd were slightly larger than ones in

  4. Trends in chloride, dissolved-solids, and nitrate concentrations in ground water, Carson Valley and Topaz Lake Areas, Douglas County, Nevada, 1959-88

    USGS Publications Warehouse

    Thodal, C.E.

    1996-01-01

    Rapid population growth in Douglas County, an area of approximately 750 square miles in west-central Nevada, has led to concern about the present and future effects of development on ground water. This report describes the results of two nonparametric statistical procedures applied to detect trends in concentrations of chloride, dissolved solids, and nitrate in ground water. The water-quality data consist of analytical results from ground-water samples collected and analyzed by the U. S. Geological Survey and ground-water-quality data provided by the Nevada Bureau of Health Protection Services for the Carson Valley and Topaz Lake areas of Douglas County, Nevada. For purposes of this study, statistical significance, expressed as the p-value, was set at 0.1. The Mann-Whitney-Wilcoxan rank-sum test detected increasing step-trends for nitrate in one of seven residential areas and for dissolved-solids concentrations throughout the study area. Decreasing step-trends for chloride and dissolved-solids concentrations were detected in the west Carson Valley area. Kendall's Tau detected monotonic trends for increasing nitrate concentrations at four domestic wells and for increasing dissolved-solids concentrations at two domestic wells. No other statistically significant trends were indicated by either test. Land-use relations to areas where increasing trends were detected suggest that the density of individual wastewater-treatment systems may exceed the capacity of soils to treat wastewater leachate.

  5. Passive equilibrium sampler for in situ measurements of freely dissolved concentrations of hydrophobic organic chemicals in sediments.

    PubMed

    Witt, Gesine; Lang, Susann-Cathrin; Ullmann, Dagny; Schaffrath, Gotja; Schulz-Bull, Detlef; Mayer, Philipp

    2013-07-16

    In this study, an equilibrium passive sampling device is introduced that facilitates the in situ measurement of hydrophobic organic chemicals bioavailability in sediments in terms of freely dissolved concentrations. The new field sampler allows SPME fibers and silicone hollow fibers to be immersed and equilibrated in situ, whereas an automated liner exchanger (ALEX) facilitates the quantitative transfer of analytes to the GC without the use of extraction solvents. The sampler was developed for environmental monitoring as follows: (1) It is of very solid construction and can be reused practically ad infinitum. (2) Fibers with varying surface to volume ratios can be exposed in parallel in order to confirm that equilibrium was reached between sampler and sediment. (3) The equilibrium times allow a temporal resolution that is suited for monitoring of both long-term trends and seasonal effects. The automated thermal desorption reduced sample treatment to a minimum and ensured cost- and time-efficient measurements while minimizing potential error sources after the sampling. The sampler is applicable in a multitude of aquatic environments, especially where currents are low and sediments are muddy and well-mixed, e.g. by bioturbation. Examples for such environments are mud flats, harbor basins, river banks, and lakes. PMID:23819657

  6. Application of high-resolution spectral absorbance measurements to determine dissolved organic carbon concentration in remote areas

    NASA Astrophysics Data System (ADS)

    Avagyan, Armine; Runkle, Benjamin R. K.; Kutzbach, Lars

    2014-09-01

    Accurate quantification of dissolved organic carbon (DOC) in surface and soil pore waters is crucial for understanding changes in water resources under the influence of climate and land use changes. Sampling and laboratory analysis of DOC content at a sufficient temporal frequency are especially difficult to achieve for natural DOC sources like the extensive boreal and arctic mire landscapes due to their remoteness. Therefore, the goals of this paper are (1) to investigate the performance of a portable, high-resolution ultraviolet-visible light spectroscopic method for determining the DOC content of surface and soil pore water samples from a boreal mire complex and (2) to compare the spectroscopic method with other DOC measurement techniques, e.g., the wet heated persulfate oxidation method and a laboratory, expulsion-based spectrophotometric method and (3) to assess different multivariate models that relate absorbance measurements with DOC contents. The study indicates that high-resolution spectroscopic measurements provide a simple, robust and non-destructive method for measuring DOC content. These measurements are of short duration (<1 min) and the sample analysis is portable, rendering this method particularly advantageous for in situ investigations at remote field locations. The study also demonstrates that if absorbances at specific wavelengths are used as proxies for DOC concentration, it is recommended to create site-specific calibration models that include more than one wavelength to achieve the optimal accuracy of the proxy-based DOC quantification.

  7. Removal of dissolved metals by zero-valent iron (ZVI): kinetics, equilibria, processes and implications for stormwater runoff treatment.

    PubMed

    Rangsivek, R; Jekel, M R

    2005-10-01

    Infiltration of stormwater runoff contaminated with metals is often questionable in several cases due to its long-term potential to cause deterioration of groundwater quality. To ensure the quality of filtrate, a pre-treatment of contaminated runoff is required. This study investigates the processes of copper and zinc ion removal from stormwater runoff using zero-valent iron (ZVI, Fe0). Kinetic and equilibrium tests were performed with laboratory-prepared and in situ stormwater runoff samples collected from roof, street and highway catchments. Based on the results, a substantial portion of Cu2+ is reduced and transformed to insoluble forms of Cu0 and Cu2O. Unlike copper, the adsorption and co-precipitation associated with freshly precipitated iron oxides play important roles for the removal of Zn2+. Investigations under various water quality conditions demonstrated a relatively minor impact on Cu2+ uptake rates. However, the different conditions apparently altered the removal stoichiometry and phases of the copper deposits. The removal rates of Zn2+ increase with higher dissolved oxygen (DO), ionic strength (IS), temperature (T) and pH. Dissolved organic carbon (DOC) in runoff samples forms complexes with metals and Fe2+, thereby kinetically decreasing the metal uptake rates. Furthermore, depending on its composition, a larger molecular weight organic fraction was found to preferentially compete for the adsorption sites. The study demonstrates that ZVI is a promising medium for achieving comparable capacity to a commercial adsorbent like granular ferric hydroxide (GFH). Long-term performance of ZVI, however, may be limited and governed by the formation of non-conductive layers of iron and cuprous oxides. PMID:16181656

  8. Heavy metal concentrations in timberline trees of eastern Tibetan Plateau.

    PubMed

    Luo, Ji; She, Jia; Yang, Peijun; Sun, Shouqin; Li, Wei; Gong, Yiwen; Tang, Ronggui

    2014-08-01

    Concentrations of 14 heavy metals (Ag, As, Cd, Co, Cr, Cu, Hg, Mo, Ni, Pb, Sb, Tl, V, and Zn) in needles, twigs, bark and xylem of spruce and fir collected at the timberline of eight sites along the Hengduan Mountains, eastern Tibetan Plateau, are reported. Twigs had the highest concentration for most of elements, while xylem had the lowest concentration. The connections between elements in twigs were much richer than other organ/tissues. Pb, Ni, As, Sb, Co, Cd, Hg, Cr and Tl which are partly through anthropogenic sources and brought in by monsoon, have been accumulated in twigs and needles by wet or dry deposition in south and east sites where are within or near pollutant sources. Under moderate pollution situation, vegetation are able to adjust the nutrient element (Cu and Zn) cycle rate, thus maintain a stable concentration level. Seldom V, Ag, and Mo are from external anthropogenic sources. Needles and twigs can be used as biomonitors for ecosystem environment when needles can simply distinguish the origin of elements and twigs are more sensitive to extra heavy metal input. PMID:24817526

  9. Effect of the spatiotemporal variability of rainfall inputs in water quality integrated catchment modelling for dissolved oxygen concentrations

    NASA Astrophysics Data System (ADS)

    Moreno Ródenas, Antonio Manuel; Cecinati, Francesca; ten Veldhuis, Marie-Claire; Langeveld, Jeroen; Clemens, Francois

    2016-04-01

    Maintaining water quality standards in highly urbanised hydrological catchments is a worldwide challenge. Water management authorities struggle to cope with changing climate and an increase in pollution pressures. Water quality modelling has been used as a decision support tool for investment and regulatory developments. This approach led to the development of integrated catchment models (ICM), which account for the link between the urban/rural hydrology and the in-river pollutant dynamics. In the modelled system, rainfall triggers the drainage systems of urban areas scattered along a river. When flow exceeds the sewer infrastructure capacity, untreated wastewater enters the natural system by combined sewer overflows. This results in a degradation of the river water quality, depending on the magnitude of the emission and river conditions. Thus, being capable of representing these dynamics in the modelling process is key for a correct assessment of the water quality. In many urbanised hydrological systems the distances between draining sewer infrastructures go beyond the de-correlation length of rainfall processes, especially, for convective summer storms. Hence, spatial and temporal scales of selected rainfall inputs are expected to affect water quality dynamics. The objective of this work is to evaluate how the use of rainfall data from different sources and with different space-time characteristics affects modelled output concentrations of dissolved oxygen in a simplified ICM. The study area is located at the Dommel, a relatively small and sensitive river flowing through the city of Eindhoven (The Netherlands). This river stretch receives the discharge of the 750,000 p.e. WWTP of Eindhoven and from over 200 combined sewer overflows scattered along its length. A pseudo-distributed water quality model has been developed in WEST (mikedhi.com); this is a lumped-physically based model that accounts for urban drainage processes, WWTP and river dynamics for several

  10. 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

  11. Evaluation of Potential pH-Driven Metal Release Due to Elevated Groundwater CO2 Concentrations

    NASA Astrophysics Data System (ADS)

    Tinnacher, R. M.; Varadharajan, C.; Zheng, L.; Spycher, N.; Birkholzer, J. T.; Trautz, R. C.; Pugh, J. D.; Esposito, R.; Nico, P. S.

    2012-12-01

    The injection of carbon dioxide (CO2) emissions from industrial sources into deep geologic formations is a potential option for the control of CO2 concentrations in the atmosphere. While the risk of CO2 migration from the storage reservoir into potable groundwater is low considering the safeguards of site characterization and permitting, it is important to understand what type of potential impacts could occur and how to identify these impacts. Elevated CO2 concentrations may potentially lead to a decrease in groundwater pH and the subsequent release of metals and ions from natural sediments into the groundwater solution. In this risk scenario, potential metal release processes, such as enhanced mineral dissolution, metal desorption and/or ion exchange reactions, may be driven by changes in groundwater pH, the presence of carbonate ligands in solution or a combination of the two. However, a detailed understanding and a distinction of pH-driven and carbonate-driven metal release reactions are important for the development of site monitoring plans and remediation strategies, required by regulations in the unlikely event of a release. Hence, in this study we characterized metal release from natural sediments into synthetic groundwater solutions at two pH conditions in order to mimic the native groundwater pH (pH ~8.5) and the low pH conditions expected in the event of elevated CO2 concentrations (pH~5). In addition, results are compared between tests performed in the presence and absence of elevated CO2. Metal release was investigated in lab-scale sequential leaching experiments using two sediment types with different organic carbon contents over a time-frame of 25 days. Supernatant solutions were monitored for pH and characterized in terms of metal concentrations (ICP-MS), total inorganic carbon (TIC) and anion composition. Furthermore, experimental results were compared with data from a field study involving the controlled release of groundwater containing dissolved

  12. A comparison of in situ vs. ex situ filtration methods on the assessment of dissolved and particulate metals at hydrothermal vents

    NASA Astrophysics Data System (ADS)

    Cotte, Laura; Waeles, Matthieu; Pernet-Coudrier, Benoît; Sarradin, Pierre-Marie; Cathalot, Cécile; Riso, Ricardo D.

    2015-11-01

    The objective of this study was to assess the impact of the filtration method (in situ vs. ex situ) on the dissolved/particulate partitioning of 12 elements in hydrothermal samples collected from the Lucky Strike vent field (Mid-Atlantic Ridge; MAR). To do so, dissolved (<0.45 μm) and particulate Mg, Li, Mn, U, V, As, Ba, Fe, Zn, Cd, Pb and Cu were measured using different techniques (HR-ICP-MS, ICP-AES and CCSA). Using in situ filtration as a baseline, we showed that ex situ filtration (on-board and on shore after freezing) resulted in an underestimation of the dissolved pool, which was counterbalanced by an overestimation of the particulate pool for almost all the elements studied. We also showed that on-board filtration was acceptable for the assessment of dissolved and particulate Mn, Mg, Li and U for which the measurement bias for the dissolved fraction did not exceed 3%. However, in situ filtration appeared necessary for the accurate assessment of the dissolved and particulate concentrations of V, As, Fe, Zn, Ba, Cd, Pb and Cu. In the case of Fe, on-board filtration underestimated the dissolved pool by up to 96%. Laboratory filtration (after freezing) resulted in a large bias in the dissolved and particulate concentrations, unambiguously discounting this filtration method for deep-sea chemical speciation studies. We discuss our results in light of the precipitation processes that can potentially affect the accuracy of ex situ filtration methods.

  13. Heavy metal and metallothionein concentrations in Atlantic Canadian seabirds.

    PubMed

    Elliott, J E; Scheuhammer, A M; Leighton, F A; Pearce, P A

    1992-01-01

    Seabird tissues, collected during the 1988 breeding season from colonies on the Atlantic coast of Canada, were analyzed for toxic metals--Cd, Hg and Pb--and 18 other trace elements. Metallothionein (MT) was measured in kidney, and kidneys and livers underwent histopathological examination. Levels of most essential trace elements appear to be closely regulated in seabird tissues; values were in good agreement with those previously reported in the published literature. Liver-Se concentrations in Leach's storm-petrels (Oceanodroma leukorrhea) (77.6 + 7.49 micrograms/g dry weight) were much higher than values normally reported for free-living birds and mammals. Cd levels varied greatly among individuals, but were always higher in kidney than in liver. Highest mean Cd concentrations (183 + 65 micrograms/g dry weight) were in kidneys of the planktivorous Leach's storm-petrels from the Gulf of St. Lawrence. A few individuals of this species had values greater than 300 micrograms/g dry weight. Cd and metallothionein (MT) concentrations were positively correlated in kidneys of Leach's storm-petrels (r = 0.692), Atlantic puffin (Fratercula arctica) (r = 0.845) and herring gull (Larus argentatus) (r = 0.866). Concentrations of total Hg varied greatly among species and individuals, but were consistently higher in liver than in kidney. Highest mean levels (21 + 28 micrograms/g) were in livers of the piscivorous double-crested cormorant (Phalacrocorax auritus) from Saint John Harbour in the Bay of Fundy. Concentrations of Hg and Se were positively correlated (r = 0.736) in livers of Leach's storm-petrel, but not in other species. Pb concentrations were consistently greatest in bone, with mean levels being highest in herring gulls from a colony in the Bay of Fundy (63 + 36 micrograms/g). Histological examination of liver and kidney failed to reveal indications of tissue damage associated with elevated levels of heavy metals. PMID:1554255

  14. Concentration of heavy metals in ash produced from Lithuanian forests

    NASA Astrophysics Data System (ADS)

    Baltrenaite, Edita; Pereira, Paulo; Butkus, Donatas; Úbeda, Xavier

    2010-05-01

    Wood ash contains important amounts of heavy metals. This quantity depends on burned specie, temperature of exposition and heat duration time. Due the high mineralization imposed by the temperatures, ash is used as lime product in agriculture and forests. Also, after a forest fire large quantities of ash are produced and distributed in soil surface. This mineralized organic matter can induce important environmental problems, including soil toxicity provoked by heavy metals leachates from ash. There is an extensive literature about heavy metals contents on ash in different species. However, it recently highlighted that the same species placed in different environments can respond diversely to same temperatures. This question is of major importance because temperature effects on severity can be a function of the plant communities instead of specie characteristics. These findings add a higher degree of complexity in the understanding of temperature effects on ash composition and consequent availability of heavy metals. The aim of this study is to compare the ash chemical heavy metal composition, Cobalt (Co), Chromium (Cr), Cooper (Cu), Silver (Ag), Lead (Pb), Nickel (Ni), Manganese (Mn) and Zinc (Zn), from Pinus sylvestris and Betula pendula, collected in key and representative areas of Lithuanian forests, located in southern, coastal and central part. Samples were collected from alive trees, taken to laboratory and air dried. Subsequently were crushed and submitted to muffle furnace at temperature of 550°C during two hours. The ash samples were digested and in a HNO3-HCl solution and then analysed with AAS. Comparisons between species and sites were performed with a Non-parametric one-way ANOVA‘s on rank transformed data followed by Tukey‘s HSD, significant at a p<0.05. Results showed significant difference between Co and Ag concentrations between Pinus sylvestris and Betula pendula. Also, significantly different concentrations of Pb, Cu, Ni and Mn were

  15. Dissolved methane concentration and flux in the coastal zone of the Southern California Bight-Mexican sector: Possible influence of wastewater

    EPA Science Inventory

    We measured dissolved methane concentrations ([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....

  16. Spatial and seasonal characteristics of dissolved heavy metals in the east and west Guangdong coastal waters, South China.

    PubMed

    Zhang, Ling; Shi, Zhen; Zhang, JingPing; Jiang, Zhijian; Wang, Fei; Huang, Xiaoping

    2015-06-15

    Heavy metal concentrations and physicochemical parameters in seawater were measured in Guangdong coastal waters, South China. Results showed that the concentrations and distribution of heavy metals varied spatially and seasonally. Generally, heavy metal concentrations in the east regions were higher than in the west. Concentrations of Pb, Zn, Cd and Cr in wet seasons were generally higher than in dry seasons owing to the seasonal differences of the river discharge, rainfall and seawater intrusion. Principal component (PC) analysis showed that PC1, PC2 and PC3 in the east were correlated to Pb+Cr+Zn+Cd, As+Cd and Cu, respectively, and they were correlated to Pb+Cr, Zn+Cu+Cd and As+Cu, respectively, in the west. That was maybe due to the differences of local heavy metal sources. The anthropogenic activities contributed more to the main sources of heavy metals, and contamination factors indicated that Zn and Pb pollution was serious in study area. PMID:25840866

  17. Year-round record of dissolved and particulate metals in surface snow at Dome Concordia (East Antarctica).

    PubMed

    Grotti, Marco; Soggia, Francesco; Ardini, Francisco; Magi, Emanuele; Becagli, Silvia; Traversi, Rita; Udisti, Roberto

    2015-11-01

    From January to December 2010, surface snow samples were collected with monthly resolution at the Concordia station (75°06'S, 123°20'E), on the Antarctic plateau, and analysed for major and trace elements in both dissolved and particulate (i.e. insoluble particles, >0.45 μm) phase. Additional surface snow samples were collected with daily resolution, for the determination of sea-salt sodium and not-sea-salt calcium, in order to support the discussion on the seasonal variations of trace elements. Concentrations of alkaline and alkaline-earth elements were higher in winter (April-October) than in summer (November-March) by a factor of 1.2-3.3, in agreement with the higher concentration of sea-salt atmospheric particles reaching the Antarctic plateau during the winter. Similarly, trace elements were generally higher in winter by a factor of 1.2-1.5, whereas Al and Fe did not show any significant seasonal trend. Partitioning between dissolved and particulate phases did not change with the sampling period, but it depended only on the element: alkaline and alkaline-earth elements, as well as Co, Cu, Mn, Pb and Zn were for the most part (>80%) in the dissolved phase, whereas Al and Fe were mainly associated with the particulate phase (>80%) and Cd, Cr, V were nearly equally distributed between the phases. Finally, the estimated marine and crustal enrichment factors indicated that Cd, Cr, Cu, Pb and Zn have a dominant anthropogenic origin, with a possible contribution from the Concordia station activities. PMID:25550109

  18. Heavy metal concentration and speciation in Sarcheshmeh soil, Kerman, Iran

    NASA Astrophysics Data System (ADS)

    Rastmanesh, Fatemeh; Moore, Farid

    2010-05-01

    Copper smelting in Sarcheshmeh copper complex poses a serious threat to soil contamination by toxic heavy metals (As, Cu, Mo, Cd, Pb, Zn). In this study assessment of induced pollution to soil is carried out and heavy metal speciation is investigated. Calculated geoaccumulation index (Igeo) using baseline values in control site indicate that the most polluted stations are those close to the smelter and also in the prevailing wind directions. Also the level of contamination is rapidly decreased with increasing distance from the smelter. This is in agreement with statistical results and soil pollution index (SPI) which also confirm decreasing elemental concentration with increasing distance from the smelter. Sequential extraction analyses indicate that metal mobility is not significant and the exchangeable fraction is negligible in most cases. The results of mobility factor calculation reflect decreasing heavy metal mobility with depth and also distance from the smelter. Furthermore, residual fraction constitutes a major fraction especially in the case of Pb, Mo and Zn. This may reflect contribution of native elements in topsoil enrichment, especially in areas distant from the smelter.

  19. Suspended sediment concentration and particle size distribution, and their relationship with heavy metal content

    NASA Astrophysics Data System (ADS)

    Sadeghi, S. H. R.; Harchegani, M. Kiani; Younesi, H. A.

    2012-02-01

    This paper aims at assessing the feasibility of suspended sediment concentration (SSC) estimation by using predictor variables of heavy metal concentration (HMC, viz., iron, chromium, zinc and nickel) transported in solution and solid. The study was conducted in the Research and Educational Forest Watershed of the Tarbiat Modares University (Kojour) which comprises an area of ca. 50000 ha. For this study, suspended sediment samples were collected from the left bank of the Kojour River twice a week, as well as during runoff events from November 2007 to June 2008. The samples were then prepared through direct digestion and finally analyzed by atomic absorption spectrophotometry (AAS). The relationship between SSC and particle size distribution (PSD) were correlated with HMC by using bivariate and multivariate regression models. Proposed models were then selected based on statistical criteria. The results showed high correlation between dissolved and particulate chromium content with efficiency coefficients beyond 77% ( P < 0.001). However, a lower relationship was found between SSC and nickel content. From these results, it is clearly shown that the HMC can practically be estimated by SSC in watersheds with different accuracy and vice versa. It is also understood that heavy metal pollution can be easily managed by controlling SSC.

  20. Concentrations and sources of metals in the Antarctic Peninsula aerosol

    SciTech Connect

    Dick, A.L. )

    1991-07-01

    Aerosol samples were collected at a remote site near the east coast of the Antarctic Peninsula during the austral summer of 1984/85. Filter samples were analyzed for Al (as a crustal reference element), marine cations (Na, K, and Ca), heavy metals (Cd, Cu, Pb, and Zn), and sulfate using atomic absorption spectrometry, isotope dilution mass spectrometry, neutron activation analysis, and ion chromatography. Ultraclean sample collection and analysis procedures used to avoid sample contamination are described in detail here. Mean concentrations of heavy metals were found to be: Cd, 0.06 pg m{sup {minus}3}; Cu, 1.0 pg m{sup {minus}3}; Pb, 4.7 pg m{sup {minus}3}; and Zn, 6.1 pg m{sup {minus}3}. These are the lowest concentrations yet determined in the troposphere, but for Pb and Zn they still indicate a significant enrichment over expected crustal concentrations. For these elements, estimated marine and volcanic contributions cannot account for this excess and suggest pollution as the dominant source even at this remote location. For Cd and Cu a dominant anthropogenic source cannot be ruled out, although current estimated of crustal, marine, a volcanic emissions could account for levels determined.

  1. 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...

  2. Contrasting distributions of dissolved gaseous mercury concentration and evasion in the North Pacific Subarctic Gyre and the Subarctic Front

    NASA Astrophysics Data System (ADS)

    Kim, Hyunji; Rhee, Tae Siek; Hahm, Doshik; Hwang, Chung Yeon; Yang, Jisook; Han, Seunghee

    2016-04-01

    The distribution of dissolved gaseous mercury (DGM) and the oxidation-reduction processes of mercury (Hg) in the surface and subsurface ocean are currently understudied despite their importance in ocean-atmosphere interactions. We investigated the Hg(0) evasion and the DGM distribution at water depths of 2-500 m in the Subarctic Front, Western Subarctic Gyre, and Bering Sea of the Northwestern Pacific. The mean DGM concentration in the surface mixed water (<10 m) and the mean Hg(0) evasion flux were significantly higher in the Subarctic Front (125±5.0 fM and 15 pmol m-2 h-1, respectively), which typically has lower nutrient levels and higher primary production, than in the Western Subarctic Gyre and the Bering Sea (74±18 fM and 3.2±1.2 pmol m-2 h-1, respectively). The variation in the chlorophyll-a concentration and extracellular protease activity predicted 54% and 48% of the DGM variation, respectively, in the euphotic zone (2-50 m). The DGM concentration in aphotic intermediate water (415±286 fM) was positively correlated to the apparent oxygen utilization (AOU; r2=0.94 and p<0.001 for the Western Subarctic Gyre and the Bering Sea; r2=0.61 and p=0.01 for the Subarctic Front), emphasizing the importance of microbial oxidation of organic matter. The DGM-to-AOU ratio in aphotic water was significantly (p<0.05, ANCOVA) higher at the Western Subarctic Gyre and Bering Sea sites (2.5±0.14) than the ratio at the Subarctic Front sites (0.89±0.27) that mainly consisted of newly formed North Pacific Intermediate Water. The overall results imply that variation of DGM and Hg(0) evasion is closely linked to primary production in euphotic water and organic remineralization in aphotic intermediate water. The oceanic alterations in these factors may induce significant modification in Hg redox speciation in the Northwestern Pacific.

  3. Environmental geochemistry of shale-hosted Ag-Pb-Zn massive sulfide deposits in northwest Alaska: Natural background concentrations of metals in water from mineralized areas

    USGS Publications Warehouse

    Kelley, K.D.; Taylor, C.D.

    1997-01-01

    Red Dog, Lik and Drenchwater are shale-hosted stratiform Ag-Pb-Zn massive sulfide deposits in the northwestern Brooks Range. Natural background concentrations of metals in waters from the undisturbed (unmined) Drenchwater prospect and Lik deposit were compared to pre-mining baseline studies conducted at Red Dog. The primary factors affecting water chemistry are the extent of exposure of the deposits, the grade of mineralization, the presence of carbonate reeks in the section, and the proportion of Fe-sulfide in the ore. Surface water samples from the Drenchwater prospect, which has pyrite-dominant mineralization exposed in outcrop, have pH values as low as 2.8 and high dissolved concentrations of metals including as much as 95 mg 1-1 Al, 270 mg 1-1 Fe, 8 ??1-1 Cd, 10 ??1-1 Pb, and 2600 ??1-1 Zn, with As up to 26 ??g1-1. Surface waters from the Red Dog deposit prior to mining were also acidic and metal-rich, however, dissolved metal concentrations in Red Dog waters were many times greater. The higher metal concentrations in Red Dog waters reflect the high Zn grades and the abundant sphalerite, pyrite, and galena that were present in outcrop prior to mining. In contrast, despite significant mineralization at the Lik deposit, carbonate rocks in the section buffer the system, resulting in less acidic, mostly near-neutral pH values with low concentrations of most metals except Zn.

  4. Attenuation of dissolved metals in neutral mine drainage in the Zambian Copperbelt.

    PubMed

    Sracek, Ondra; Filip, Jan; Mihaljevič, Martin; Kříbek, Bohdan; Majer, Vladimír; Veselovský, František

    2011-01-01

    Behaviour of metals like Cu and Co was studied in nearly neutral (pH ≥ 6.4) mine drainage seepage in a stream downgradient of a tailing dam at Chambishi site in the Copperbelt of Zambia. They are attenuated by precipitation of ferruginous ochres that incorporate significant quantities of metals. Using chemical analysis, X-ray powder diffraction and Mössbauer spectroscopy, we show that the ochres are composed mostly of amorphous ferric hydroxide. Close to the seepage face, the total Fe content of ochres increases due to precipitation of amorphous ferric hydroxide, but total Fe in sediment decreases further downstream. The stream then flows through wetland (dambo) where the remaining fraction of metals is removed. During rainy periods, increased flow rate may result in re-suspension of ochres, increasing thus the mobility of metals. Major ions like sulphate are conservative at the start of the dry period (May), but gypsum may probably precipitate later at the end of the dry period. Sequential extractions of bulk sediments indicate that Mn behaves differently to Fe, with a trend of increasing Mn with distance from the tailing dam. There is much more Fe than Mn in residual (Aqua Regia) fraction, indicating that amorphous ferric hydroxides are transformed to more crystalline phases deeper in sediment. Environmental impact of mine drainage is relatively limited due to its neutral character. PMID:20140501

  5. DISSOLVED ORGANIC CARBON CHARACTERISTICS IN METAL-RICH WATERS AND THE IMPLICATIONS FOR COPPER AQUATIC TOXICITY

    EPA Science Inventory

    This research will aim to quantify the effects of fractionation between DOC, HFO, HAO, free copper and the behavior of resultant free DOC in the water column on the toxicological effects of copper. Fractionation between DOC, free metals and iron (Fe) and aluminum (Al) hydro...

  6. Continuous emission monitoring of metal aerosol concentrations in atmospheric air

    NASA Astrophysics Data System (ADS)

    Gomes, Anne-Marie; Sarrette, Jean-Philippe; Madon, Lydie; Almi, Abdenbi

    1996-11-01

    Improvements of an apparatus for continuous emission monitoring (CEM) by inductively coupled plasma atomic emission spectrometry (ICP-AES) of metal aerosols in air are described. The method simultaneously offers low operating costs, large volume of tested air for valuable sampling and avoids supplementary contamination or keeping of the air pollutant concentrations. Questions related to detection and calibration are discussed. The detection limits (DL) obtained for the eight pollutants studied are lower than the recommended threshold limit values (TLV) and as satisfactory as the results obtained with other CEM methods involving air-argon plasmas.

  7. Effects of Land Use on Stable Carbon Isotopic Composition and Concentration of Dissolved Organic Carbon (DOC) and Dissolved Inorganic Carbon (DIC) in Southeastern US Piedmont Headwater Streams

    EPA Science Inventory

    Stable carbon isotopic composition (delta 13C) and concentrations of DOC and DIC were measured in stream water samples collected monthly in 15 headwater streams from an area with extensive poultry and cattle production and a rapidly growing human population. Linear regression te...

  8. Trout density and health in a stream with variable water temperatures and trace element concentrations: does a cold-water source attract trout to increased metal exposure?

    PubMed

    Harper, David D; Farag, Aïda M; Hogstrand, Christer; Macconnell, Elizabeth

    2009-04-01

    A history of hard-rock mining has resulted in elevated concentrations of heavy metals in Prickly Pear Creek (MT, USA). Remediation has improved water quality; however, dissolved zinc and cadmium concentrations still exceed U.S. Environmental Protection Agency water-quality criteria. Physical habitat, salmonid density, fish health, and water quality were assessed, and metal concentrations in fish tissues, biofilm, and macroinvertebrates were determined to evaluate the existing condition in the watershed. Cadmium, zinc, and lead concentrations in fish tissues, biofilm, and invertebrates were significantly greater than those at the upstream reference site and an experimental site farther downstream of the confluence. Fish densities were greatest, and habitat quality for trout was better, downstream of the confluence, where water temperatures were relatively cool (16 degrees C). Measures of fish health (tissue metal residues, histology, metallothionein concentrations, and necropsies), however, indicate that the health of trout at this site was negatively affected. Trout were in colder but more contaminated water and were subjected to increased trace element exposures and associated health effects. Maximum water temperatures in Prickly Pear Creek were significantly lower directly below Spring Creek (16 degrees C) compared to those at an experimental site 10 km downstream (26 degrees C). Trout will avoid dissolved metals at concentrations below those measured in Prickly Pear Creek; however, our results suggest that the preference of trout to use cool water temperatures may supersede behaviors to avoid heavy metals. PMID:19391677

  9. Trout density and health in a stream with variable water temperatures and trace element concentrations: does a cold-water source attract trout to increased metal exposure?

    USGS Publications Warehouse

    Harper, D.D.; Farag, A.M.; Hogstr, C.; MacConnell, E.

    2009-01-01

    A history of hard-rock mining has resulted in elevated concentrations of heavy metals in Prickly Pear Creek (MT. USA). Remediation has improved water quality; however, dissolved zinc and cadmium concentrations still exceed U.S. Environmental Protection Agency water-quality criteria. Physical habitat, salmonid density, fish health, and water quality were assessed, and metal concentrations in fish tissues, biofilm, and macroinvertebrates were determined to evaluate the existing condition in the watershed. Cadmium, zinc, and lead concentrations in fish tissues, biofilm, and invertebrates were significantly greater than those at the upstream reference site and an experimental site farther downstream of the confluence. Fish densities were greatest, and habitat quality for trout was better, downstream of the confluence, where water temperatures were relatively cool (16??C). Measures of fish health (tissue metal residues, histology, metallothionein concentrations, and necropsies), however, indicate that the health of trout at this site was negatively affected. Trout were in colder but more contaminated water and were subjected to increased trace element exposures and associated health effects. Maximum water temperatures in Prickly Pear Creek were significantly lower directly below Spring Creek (16??C) compared to those at an experimental site 10 km downstream (26??C). Trout will avoid dissolved metals at concentrations below those measured in Prickly Pear Creek; however, our results suggest that the preference of trout to use cool water temperatures may supersede behaviors to avoid heavy metals. ?? 2009 SETAC.

  10. Microbial community evolution during simulated managed aquifer recharge in response to different biodegradable dissolved organic carbon (BDOC) concentrations.

    PubMed

    Li, Dong; Alidina, Mazahirali; Ouf, Mohamed; Sharp, Jonathan O; Saikaly, Pascal; Drewes, Jörg E

    2013-05-01

    This study investigates the evolution of the microbial community in laboratory-scale soil columns simulating the infiltration zone of managed aquifer recharge (MAR) systems and analogous natural aquifer sediment ecosystems. Parallel systems were supplemented with either moderate (1.1 mg/L) or low (0.5 mg/L) biodegradable dissolved organic carbon (BDOC) for a period of six months during which time, spatial (1 cm, 30 cm, 60 cm, 90 cm, and 120 cm) and temporal (monthly) analyses of sediment-associated microbial community structure were analyzed. Total microbial biomass associated with sediments was positively correlated with BDOC concentration where a significant decline in BDOC was observed along the column length. Analysis of 16S rRNA genes indicated dominance by Bacteria with Archaea comprising less than 1 percent of the total community. Proteobacteria was found to be the major phylum in samples from all column depths with contributions from Betaproteobacteria, Alphaproteobacteria and Gammaproteobacteria. Microbial community structure at all the phylum, class and genus levels differed significantly at 1 cm between columns receiving moderate and low BDOC concentrations; in contrast strong similarities were observed both between parallel column systems and across samples from 30 to 120 cm depths. Samples from 1 cm depth of the low BDOC columns exhibited higher microbial diversity (expressed as Shannon Index) than those at 1 cm of moderate BDOC columns, and both increased from 5.4 to 5.9 at 1 cm depth to 6.7-8.3 at 30-120 cm depths. The microbial community structure reached steady state after 3-4 months since the initiation of the experiment, which also resulted in an improved DOC removal during the same time period. This study suggested that BDOC could significantly influence microbial community structure regarding both composition and diversity of artificial MAR systems and analogous natural aquifer sediment ecosystems. PMID:23490107

  11. Using in-situ spectrophotometric sensors to monitoring dissolved organic carbon concentration: our S::CAN experience

    NASA Astrophysics Data System (ADS)

    Coleman, Martin; Waldron, Susan; Scott, Marian; Drew, Simon

    2013-04-01

    Dissolved organic carbon, (DOC), is the component of the organic carbon that can pass through a membrane filter, with the accepted maximum pore size of 0.7 μm. There is growing interest in high resolution time series of such data e.g. heterotrophic respiration of DOC in freshwater systems can fuel atmospheric CO2 efflux so observing variation in DOC concentration, [DOC], is meaningful. Field deployable sensors, capable of measuring [DOC] on a continuous basis, have the potential to provide us with a far higher resolution time series data than we can obtain through manual sampling. At a catchment area draining Europe's largest windfarm, Whitelee, we have deployed an S::CAN Spectrolyser. This device scans wavelengths from 200 to 735nm, generating a spectral fingerprint and then, using an inbuilt algorithm, returns a value for the DOC concentration, termed DOC-equivalent, [DOC-eq]. The Spectrolyser also estimates other parameters such as total organic carbon and the true colour of the water. Unfortunately, our field Spectrolyser [DOC] are different from lab based measurement of [DOC] of the same field filtered samples (measured using a Thermalox high temperature catalytic oxidation system). Comparing 28 lab measured [DOC] with Spectrolyser [DOC-eq] shows an average difference of 7.6 mg/l C. Here we discuss our interpretation of why this disparity exists and how to accommodate this offset such that accuracy is improved. We have tried various methods of keeping the lens and path length clean through brushing, acid cleaning and the recent installation of a high pressure air hose (recommended by S::CAN). We will compare output before and after this installation. Further complexity is added because light may be absorbed by other components of the field sample, such as particulate material, and this could compromise the estimated [DOC-eq]. [DOC] may be estimated using absorption measurements made at 254nm and 340nm (Tipping et al, 2009). We have implemented this formula

  12. Heavy metal concentrations in Louisiana waterways, sediments, and biota

    SciTech Connect

    Bundy, K.J.; Berzins, D.

    1994-12-31

    In this investigation polarographic methods (along with GFAAS and ICP) have been used to study the distribution of lead and chromium in Bayou Trepagnier and Devil`s Swamp. Both laboratory and field research have been conducted. Separation and extraction methodology appropriate for analysis of the contaminants at these sites have been developed. Particular attention has been paid to extraction methods for chromium which do not lead to valence state conversion. The availability of such techniques is essential to take full advantage of polarography, a method capable of performing speciation analysis. The results indicate that there is a very inhomogeneous distribution of heavy metals in these environments. In Devil`s Swamp, for example, separation and analysis of aqueous and variously sized particulate moieties in the water and sediment compartments were conducted to determine the partition of lead between them. The results showed that the average lead content was 14.7 ppb and 19.8 ppm, respectively, in these compartments. Apparently bull frogs in Devil`s Swamp can bioaccumulate lead (compared to the measured water level), since the muscle concentration was found to be about 0.6 ppm. This phenomenon is being investigated in a Xenopus frog laboratory model of heavy metal uptake. The basic methodology validated in this study should be fairly generally applicable to assays of other heavy metals.

  13. Number concentrations of fine and ultrafine particles containing metals

    NASA Astrophysics Data System (ADS)

    Tolocka, Michael P.; Lake, Derek A.; Johnston, Murray V.; Wexler, Anthony S.

    Typical classification schemes for large data sets of single-particle mass spectra involve statistical or neural network analysis. In this work, a new approach is evaluated in which particle spectra are pre-selected on the basis of an above threshold signal intensity at a specified m/ z (mass to charge ratio). This provides a simple way to identify candidate particles that may contain the specific chemical component associated with that m/ z. Once selected, the candidate particle spectra are then classified by the fast adaptive resonance algorithm, ART 2-a, to confirm the presence of the targeted component in the particle and to study the intra-particle associations with other chemical components. This approach is used to characterize metals in a 75,000 particle data set obtained in Baltimore, Maryland. Particles containing a specific metal are identified and then used to determine the size distribution, number concentration, time/wind dependencies and intra-particle correlations with other metals. Four representative elements are considered in this study: vanadium, iron, arsenic and lead. Number concentrations of ambient particles containing these elements can exceed 10,000 particles cm -3 at the measurement site. Vanadium, a primary marker for fuel oil combustion, is observed from all wind directions during this time period. Iron and lead are observed from the east-northeast. Most particles from this direction that contain iron also contain lead and most particles that contain lead also contain iron, suggesting a common emission source for the two. Arsenic and lead are observed from the south-southeast. Particles from this direction contain either arsenic or lead but rarely both, suggesting different sources for each element.

  14. Factors affecting sorption of nitro explosives to biochar: pyrolysis temperature, surface treatment, competition, and dissolved metals.

    PubMed

    Oh, Seok-Young; Seo, Yong-Deuk

    2015-05-01

    The application of rice straw-derived biochar for removing nitro explosives, including 2,4-dinitrotoluene (DNT), 2,4,6-trinitrotoluene (TNT), and hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), from contaminated water was investigated through batch experiments. An increase in the pyrolysis temperature from 250 to 900°C in general led to higher pH, surface area, cation exchange capacity (CEC), point of zero charge, and C:O ratio of biochar. The maximum sorption capacity estimated by a mixed sorption-partition model increased when pyrolysis temperatures were elevated from 250 to 900°C, indicating that C content and aromaticity of biochar were strongly related to the sorption of nitro explosives to biochar. Surface treatment with acid or oxidant increased the sorption capacity of biochar for the two strong π-acceptor compounds (DNT and TNT) but not for RDX. However, the enhancement of sorption capacity was not directly related to increased surface area and CEC. Compared with single-sorption systems, coexistence of explosives or cationic metals resulted in decreased sorption of each explosive to biochar, suggesting that sorption of nitro explosives and cationic metals to electron-rich portions in biochar was competitive. Our results suggest that π-π electron donor acceptor interactions are main sorption mechanisms and that changing various conditions can enhance or reduce the sorption of nitro explosives to biochar. PMID:26024263

  15. Land Use Controls on Stream and Lake Dissolved Silica Concentrations: A Case Study from the Finger Lakes, Central New York State, USA.

    NASA Astrophysics Data System (ADS)

    Halfman, J. D.

    2014-12-01

    Bedrock geology, climate and time are important controls on chemical weathering and release of dissolved silica. Forested land vs. other land uses was recently hypothesized as another control. The Finger Lakes region is an ideal natural laboratory to test this hypothesis as local watersheds vary in area, bedrock and agricultural to forested land cover in this rural setting. Annual mean dissolved silica data from 11 watersheds in our ongoing monitoring program ranged from 100 to 4,000 μg/L Si, analyzing filtered (0.45 μm) samples by spectrophotometer (molybdate indicator with metol/oxalic acid reagents). Like earlier work, only forested land use (12 to 73%) correlated to the mean silica concentrations (r2 = 0.3), which improves (r2 = 0.6) when a small, primarily (24%) developed watershed is excluded from the correlation. Bedrock (Devonian carbonates, 0 to 8% and clastics, 0 to 99% covered by till) and basin area (10 to 500 km2) did not correlate (r2 <= 0.1). Event and base flow samples of an agricultural (64%) watershed revealed peak to base flow fluctuations in silica concentrations that more closely mimic nitrates and other groundwater solutes than suspended particles, phosphates and other runoff signature parameters. Annual mean epilimnion and hypolimnion dissolved silica data from the 8 easternmost Finger Lakes in our ongoing monitoring program ranged from 250 to 1,500 μg/L Si. Forested cover (30 to 75%) positively correlated to epilimnion silica concentrations (r2 = 0.6). Lake water residence time (1 to 17 yr) negatively correlated to hypolimnion silica concentrations (r2 = 0.5). Agricultural land use, bedrock, and productivity indicators (chlorophyll-a, total phosphate, and secchi disk depth) lacked correlation (r2 <= 0.1). It suggested that land use impacts stream and, surprisingly, lake dissolved silica chemistry. Biogeochemical processes in the lakes like diatom uptake appears to increasingly decrease silica concentrations in lakes with longer residence

  16. Viral Lysis of Cells Influences The Concentration and Compostion of Dissolved Organic Matter and The Formation of Organic Aggregates (marine Snow)

    NASA Astrophysics Data System (ADS)

    Weinbauer, M. G.; Peduzzi, P.

    The effect of moderately (ca. 2.5 fold) increasing the concentration of the virus-size fraction (VSF) of seawater on the chemical composition of the dissolved organic mat- ter (DOM) pool during the formation of organic aggregates (marine snow) was tested experimentally with seawater samples collected in the Northern Adriatic Sea. The VSF enrichment did not significantly change the concentration of selected DOM com- pounds, whereas viral abundance was ca. 2-fold higher. During long-term experiments (40 - 200 hrs), bacterial abundance was on average 25% lower in the VSF amended than in the control incubations, and the frequency of visibly infected cells was stimu- lated by ca. 50%. VSF delayed the development of phytoplankton blooms (diatoms), but in the end of the experiments, Chl a concentrations in the VSF amended incuba- tions exceeded those in the control incubations. The VSF enrichment caused an enrich- ment of Serine and Threonine in the dissolved hydrolysable amino acid (AA) fraction indicative of viral lysis of diatoms. Bulk dissolved free AA acid and monomeric car- bohydrate (CHO) concentrations were repressed, whereas bulk dissolved hydrolysable AA and CHO concentrations were stimulated in the VSF enriched incubations. Viral lysis was likely the major reason for the stimulation of hydrolysable DOM. The for- mation of organic aggregates was repressed by the VSF enrichment, but the aggregates were larger and more persistent in the VSF amended than in the control incubations. Stimulation of hydrolysable DOM and sticky viral lysis products might be the reason for the larger and more persistent aggregates. This demonstrates that bioactive mate- rial in the VSF of seawater can have major implications for primary production and the cycling of organic carbon in the ocean.

  17. Characterizing the production and retention of dissolved iron as Fe(II) across a natural gradient in chlorophyll concentrations in the Southern Drake Passage - Final Technical Report

    SciTech Connect

    Katherine Barbeau

    2007-04-10

    . As a co-PI in the NSF/OPP-funded project, I was responsible for iron addition incubation and radiotracer experiments, and analysis of iron chemistry, including iron-organic speciation. This final technical report describes the results of my DOE funded project to analyse reduced iron species using an FeLume flow injection analysis chemiluminescence system as an extension of my work on the NSF/OPP project. On the cruise in 2004, spatial and temporal gradients in Fe(II) were determined, and on-board incubations were conducted to study Fe(II) lifetime and production. Following the cruise a further series of experiments was conducted in my laboratory to study Fe(II) lifetimes and photoproduction under conditions typical of high latitude waters. The findings of this study suggest that, in contrast to results observed during mesoscale iron addition experiments, steady-state levels of Fe(II) are likely to remain low (below detection) even within a significant gradient in dissolved Fe concentrations produced as a result of natural iron enrichment processes. Fe(II) is likely to be produced, however, as a reactive intermediate associated with photochemical reactions in surface waters. While Fe(II) lifetimes measured in the field in this study were commensurate with those determined in previously published Southern Ocean work, Fe(II) lifetimes reflective of realistic Southern Ocean environmental conditions have proven difficult to determine in a laboratory setting, due to contamination by trace levels of H2O2. Laboratory experiments demonstrated that direct ligand-to-metal charge transfer reactions of strong Fe(III)-organic complexes do appear to be a viable source of available Fe(II) in Antarctic waters, and further studies are needed to characterize the temperature dependence of this phenomenon.

  18. B/Ca in coccoliths and relationship to calcification vesicle pH and dissolved inorganic carbon concentrations

    NASA Astrophysics Data System (ADS)

    Stoll, Heather; Langer, Gerald; Shimizu, Nobumichi; Kanamaru, Kinuyo

    2012-03-01

    Coccolithophorid algae are microscopic but prolific calcifiers in modern and ancient oceans. When the pH of seawater is modified, as may occur in the future due to ocean acidification, different species and strains of coccolithophorids have exhibited diverse calcification responses in laboratory culture. Since their biomineralization is a completely intracellular process, it is unclear why their response should be affected by extracellular seawater pH. Variations in the B/Ca in coccoliths are potential indicators of pH shifts in the intracellular coccolith vesicle where calcification occurs, because B/Ca in abiogenic calcites increases at higher pH due to the greater abundance of borate ions, the only B species incorporated into calcite. We used a SIMS ion probe to measure B/Ca of coccoliths from three different strains of Emiliania huxleyi and one strain of Coccolithus braarudii braarudii cultured under different seawater pH conditions to ascertain if the B/Ca can be used to elucidate how coccolithophorids respond to changing ocean pH. These data are interpreted with the aid of a conceptual model of cellular boron acquisition by coccolithophorids. Based on uptake in other plants, we infer that boron uptake by coccolithophorid cells is dominated by passive uptake of boric acid across the lipid bilayer. Subsequently, in the alkaline coccolith vesicle (C.V.), boron speciates according to the C.V. pH, and borate is incorporated into the coccolith. At increasing seawater pH, the relative abundance of the neutral boric acid in seawater decreases, lowering the potential B flux into the cell. Homeostasis or constant pH of the coccolith vesicle results in a decrease of the B/Ca in the coccolith with increasing seawater pH. In contrast, if coccolith vesicle pH increases with increasing seawater pH, then the B/Ca will increase as the fraction of borate in the coccolith vesicle increases. The coccolith B/Ca is also expected to depend inversely on the dissolved inorganic

  19. The effect of two initiator/stabilizer concentrations in a metal primer on bond strengths of a composite to a base metal alloy.

    PubMed

    Richards, N D; Eichmiller, F; Dickens, S V; Simoni, F V

    1993-03-01

    This study examined the effect of three additives, amine, peroxide and stabilizer, in two concentrations in a metal primer on the adhesion between a cast metal alloy and a resin composite using a 23 factorial statistical design. The additives, benzoylperoxide (BPO) used at 1% or 2% w/w and N,N-dimethyl-p-toluidine (DMPT) at 0.5% or 1.8% w/w are polymerization initiators. The third additive, butylated hydroxytoluene (BHT) at 0.01% or 0.03% w/w, is used as a stabilizer. BPO and BHT were dissolved in an acetone solution containing 20% of the adhesive resin pyromellitic glyceroldimethacrylate (PMGDM). DMPT was in a separate acetone solution. Equal portions of each solution were mixed and applied to a sandpaper-abraded, air-blasted nickel-chrome alloy. Bonding resin and composite were applied over the primer and stored overnight in water. Bond strengths were determined by shearing the composite from the metal at a cross head speed of 0.5 mm/min. Increasing the concentration of BPO caused a statistically significant increase in bond strength. A 3-way analysis of variance (ANOVA) at p<0.05 showed that, of the interactions, only the one between DMPT and BPO was significant, with lower concentrations of DMPT being less sensitive to changes in BPO concentration. PMID:8595848

  20. Production of channel catfish and channel x blue hybrid catfish subjected to two minimum dissolved oxygen concentrations

    Technology Transfer Automated Retrieval System (TEKTRAN)

    As the channel x blue hybrid catfish is stocked by an increasing number of catfish farmers, it is important to quantify the production response of this fish to dissolved oxygen management strategies. The purpose of this study was to compare the production and water quality responses of the channel x...

  1. Investigating the Temporal Effects of Metal-Based Coagulants to Remove Mercury from Solution in the Presence of Dissolved Organic Matter.

    PubMed

    Henneberry, Yumiko; Kraus, Tamara E C; Krabbenhoft, David P; Horwath, William R

    2016-01-01

    The presence of mercury (Hg), particularly methylmercury (MeHg), is a concern for both human and ecological health as MeHg is a neurotoxin and can bioaccumulate to lethal levels in upper trophic level organisms. Recent research has demonstrated that coagulation with metal-based salts can effectively remove both inorganic mercury (IHg) and MeHg from solution through association with dissolved organic matter (DOM) and subsequent flocculation and precipitation. In this study, we sought to further examine interactions between Hg and DOM and the resulting organo-metallic precipitate (floc) to assess if (1) newly added IHg could be removed to the same extent as ambient IHg or whether the association between IHg and DOM requires time, and (2) once formed, if the floc has the capacity to remove additional Hg from solution. Agricultural drainage water samples containing ambient concentrations of both DOM and IHg were spiked with a traceable amount of isotopically enriched IHg and dosed with ferric sulfate after 0, 1, 5, and 30 days. Both ambient and newly added IHg were removed within hours, with 69-79 % removed. To a separate sample set, isotopically enriched IHg was added to solution after floc had formed. Under those conditions, 81-95 % of newly added Hg was removed even at Hg concentrations 1000-fold higher than ambient levels. Results of this study indicate coagulation with ferric sulfate effectively removes both ambient and newly added IHg entering a system and suggests rapid association between IHg and DOM. This work also provides new information regarding the ability of floc to remove additional Hg from solution even after it has formed. PMID:26330169

  2. Investigating the Temporal Effects of Metal-Based Coagulants to Remove Mercury from Solution in the Presence of Dissolved Organic Matter

    NASA Astrophysics Data System (ADS)

    Henneberry, Yumiko; Kraus, Tamara E. C.; Krabbenhoft, David P.; Horwath, William R.

    2016-01-01

    The presence of mercury (Hg), particularly methylmercury (MeHg), is a concern for both human and ecological health as MeHg is a neurotoxin and can bioaccumulate to lethal levels in upper trophic level organisms. Recent research has demonstrated that coagulation with metal-based salts can effectively remove both inorganic mercury (IHg) and MeHg from solution through association with dissolved organic matter (DOM) and subsequent flocculation and precipitation. In this study, we sought to further examine interactions between Hg and DOM and the resulting organo-metallic precipitate (floc) to assess if (1) newly added IHg could be removed to the same extent as ambient IHg or whether the association between IHg and DOM requires time, and (2) once formed, if the floc has the capacity to remove additional Hg from solution. Agricultural drainage water samples containing ambient concentrations of both DOM and IHg were spiked with a traceable amount of isotopically enriched IHg and dosed with ferric sulfate after 0, 1, 5, and 30 days. Both ambient and newly added IHg were removed within hours, with 69-79 % removed. To a separate sample set, isotopically enriched IHg was added to solution after floc had formed. Under those conditions, 81-95 % of newly added Hg was removed even at Hg concentrations 1000-fold higher than ambient levels. Results of this study indicate coagulation with ferric sulfate effectively removes both ambient and newly added IHg entering a system and suggests rapid association between IHg and DOM. This work also provides new information regarding the ability of floc to remove additional Hg from solution even after it has formed.

  3. Investigating the temporal effects of metal-based coagulants to remove mercury from solution in the presence of dissolved organic matter

    USGS Publications Warehouse

    Henneberry, Yumiko K.; Kraus, Tamara; Krabbenhoft, David P.; Horwath, William R.

    2015-01-01

    The presence of mercury (Hg), particularly methylmercury (MeHg), is a concern for both human and ecological health as MeHg is a neurotoxin and can bioaccumulate to lethal levels in upper trophic level organisms. Recent research has demonstrated that coagulation with metal-based salts can effectively remove both inorganic mercury (IHg) and MeHg from solution through association with dissolved organic matter (DOM) and subsequent flocculation and precipitation. In this study, we sought to further examine interactions between Hg and DOM and the resulting organo-metallic precipitate (floc) to assess if (1) newly added IHg could be removed to the same extent as ambient IHg or whether the association between IHg and DOM requires time, and (2) once formed, if the floc has the capacity to remove additional Hg from solution. Agricultural drainage water samples containing ambient concentrations of both DOM and IHg were spiked with a traceable amount of isotopically enriched IHg and dosed with ferric sulfate after 0, 1, 5, and 30 days. Both ambient and newly added IHg were removed within hours, with 69–79 % removed. To a separate sample set, isotopically enriched IHg was added to solution after floc had formed. Under those conditions, 81–95 % of newly added Hg was removed even at Hg concentrations 1000-fold higher than ambient levels. Results of this study indicate coagulation with ferric sulfate effectively removes both ambient and newly added IHg entering a system and suggests rapid association between IHg and DOM. This work also provides new information regarding the ability of floc to remove additional Hg from solution even after it has formed.

  4. Metals and PCB concentrations in mussels from Long Island Sound

    SciTech Connect

    Greig, R.A.; Sennefelder, G.

    1985-09-01

    Metals and polychlorinated biphenyls (PCBs) are contaminants of concern in Long Island Sound. To gain an understanding of contaminant inputs from the major rivers of Connecticut into the Sound, a continuous measurement over time should be made of the concentrations of contaminants in the river water. Analyses of water for contaminants are quite complex and often ambiguous because of the dynamic nature of river water. To alleviate this problem, the mussel, Mytilus edulis, has been proposed by various researchers to be a good subject for monitoring contaminants present in the water column. For this study, mussels were collected from the mouths of various rivers and inshore areas along the Connecticut shoreline and analyzed for cadmium, copper, and PCBs.

  5. High Temperature Concentrated Solar Power Using Liquid Metal

    NASA Astrophysics Data System (ADS)

    Henry, Asegun

    One of the most attractive ways to try and reduce the cost of concentrated solar power (CSP) is to increase the system efficiency and the biggest loss in the system occurs in the conversion of heat to electricity via heat engine. Heat engines that utilize turbomachinery currently operate near their thermodynamic limitations and thus one of the only ways to improve heat engine efficiency is to increase the turbine inlet temperature. Significant effort is being devoted to the development of supercritical CO2 heat engines, but the most efficient heat engines are combined cycles, which reach efficiencies as high as 60%. However, such heat engines require turbine inlet temperatures ~1300-1500C, which is far beyond what is currently feasible with the state of the art molten salt infrastructure. In working towards the development of a system that can operate in the 1300-1500C temperature range, the most significant challenges lie in the materials and forming functional and reliable components out of new materials. One of the most attractive options from a cost and heat transfer perspective is to use liquid metals, such as tin and aluminum-silicon alloys along with a ceramic based infrastructure. This talk will overview ongoing efforts in the Atomistic Simulation and Energy (ASE) research group at Georgia Tech to develop prototype components such as an efficient high temperature cavity receiver, pumps and valves that can make a liquid metal based CSP infrastructure realizable.

  6. Fatigue stress concentration and notch sensitivity in nanocrystalline metals

    DOE PAGESBeta

    Furnish, Timothy A.; Boyce, Brad L.; Sharon, John A.; O’Brien, Christopher J.; Clark, Blythe G.; Arrington, Christian L.; Pillars, Jamin R.

    2016-03-11

    Recent studies have shown the potential for nanocrystalline metals to possess excellent fatigue resistance compared to their coarse-grained counterparts. Although the mechanical properties of nanocrystalline metals are believed to be particularly susceptible to material defects, a systematic study of the effects of geometric discontinuities on their fatigue performance has not yet been performed. In the present work, nanocrystalline Ni–40 wt%Fe containing both intrinsic and extrinsic defects were tested in tension–tension fatigue. The defects were found to dramatically reduce the fatigue resistance, which was attributed to the relatively high notch sensitivity in the nanocrystalline material. Microstructural analysis within the crack-initiation zonesmore » underneath the defects revealed cyclically-induced abnormal grain growth (AGG) as a predominant deformation and crack initiation mechanism during high-cycle fatigue. Furthermore, the onset of AGG and the ensuing fracture is likely accelerated by the stress concentrations, resulting in the reduced fatigue resistance compared to the relatively defect-free counterparts.« less

  7. Sources and concentrations of dissolved solids and selenium in the San Joaquin River and its tributaries, California, October 1985 to March 1987

    SciTech Connect

    Clifton, D.G.; Gilliom, R.J.

    1989-01-01

    Sources and concentrations of dissolved solids and selenium in the San Joaquin River and its tributaries, California, were assessed by a mass-balance approach to determine the effects of tile-drain water and irrigation-return flows on the river. The study included low-flow periods from October 1985 to mid-February 1986 and mid-May 1986 through March 1987, and a high-flow period from mid-February to mid-May 1985. During the combined low-flow period, the dissolved-solids load from eastside tributaries and the upper San Joaquin River accounted for only 18% of the total load at Vernalis, located farthest downstream, even though they accounted for 71% of the stream flow. Salt and Mud Sloughs contributed 40% of the dissolved-solids load but only 9% of stream flow. Unmeasured sources of dissolved solids contributed about 42% of the total load during low flow. In contrast, Salt and Mud Sloughs, which receive most of the tile-drain water that enters the river, contributed almost 80% of the total selenium load to the river, and loading of selenium concentrations were highest in Salt and Mud Sloughs and decreased downstream in the San Joaquin River with dilution from eastside tributaries. A State standard for dissolved solids of 500 mg/L was exceeded 11% of the time in the San Joaquin River at Vernalis. The US Environmental Protection Agency's 4-day average aquatic-life criterion of 5 micrograms/L of selenium was exceeded in more than 60% of the samples from the sloughs and in about 20% of the samples from the San Joaquin River, just downstream of the Merced River. 23 refs., 8 figs., 6 tabs.

  8. Effects of environmentally relevant concentrations of metallic compounds on the flatfish Scophthalmus maximus: biomarkers of neurotoxicity, oxidative stress and metabolism.

    PubMed

    Nunes, Bruno; Brandão, Fátima; Sérgio, Tânia; Rodrigues, Sara; Gonçalves, Fernando; Correia, Alberto Teodorico

    2014-06-01

    Flatfish species, such as the turbot (Scophthalmus maximus), are common targets for toxic effects, since they are exposed through the food chain (ingestion of contaminated preys) and are in direct contact with the waterborne contaminant and sediments. Furthermore, these fish species live in close proximity to interstitial water that frequently dissolves high amounts of contaminants, including metals. Despite this significant set of characteristics, the present knowledge concerning flatfish contamination and toxicity by metals is still scarce. To attain the objective of assessing the effects of metals on a flatfish species, S. maximus specimens were chronically exposed to lead, copper and zinc, at ecologically relevant concentrations, and biochemical (oxidative stress: catalase and glutathione S-transferases activities, and lipid peroxidation; neurotoxicity: cholinesterase activity) parameters were assessed on selected tissues (gills and liver). Copper had no significant effects on all tested parameters; lead was causative of significant increases in liver GSTs activities and also in lipoperoxidation of gill tissue; exposure to zinc caused a significant increase in catalase activity of gill tissue. None of the tested metals elicited noteworthy effects in terms of neurotoxicity. The obtained results showed that only the metal lead is of some environmental importance, since it was able to cause deleterious modifications of oxidative nature at relevant concentrations. PMID:24595748

  9. Leaching of chloride, sulphate, heavy metals, dissolved organic carbon and phenolic organic pesticides from contaminated concrete.

    PubMed

    Van Praagh, M; Modin, H

    2016-10-01

    Concrete samples from demolition waste of a former pesticide plant in Sweden were analysed for total contents and leachate concentrations of potentially hazardous inorganic substances, TOC, phenols, as well as for pesticide compounds such as phenoxy acids, chlorophenols and chlorocresols. Leachates were produced by means of modified standard column leaching tests and pH-stat batch tests. Due to elevated contents of chromium and lead, as well as due to high chloride concentrations in the first leachate from column tests at L/S 0.1, recycling of the concrete as a construction material in groundworks is likely to be restricted according to Swedish guidelines. The studied pesticide compounds appear to be relatively mobile at the materials own pH>12, 12, 9 and 7. Potential leaching of pesticide residues from recycled concrete to ground water and surface water might exceed water quality guidelines for the remediation site and the EU Water Framework Directive. Results of this study stress the necessity to systematically study the mechanism behind mobility of organic contaminants from alkaline construction and demolition wastes rather than rely on total content limit values. PMID:27449537

  10. Comparison of metal concentrations in three species of mosses and metal freights in bulk precipitations.

    PubMed

    Thöni, L; Schnyder, N; Krieg, F

    1996-03-01

    Concentration of 25 trace metals in mosses ( Hylocomium splendens, Pleurozium schreberi and Hypnum cupressiforme) are compared with bulk deposition freights (Bergerhoff method) at 3 sites in Switzerland, one on the plateau, a second in the northern prealps and a third in the southern alps. The three moss species are interchangeable and the atmospheric background deposition can be estimated with sufficient accuracy for Ag, Al, As, Cd, Ce, Co, Cr, Cu, Fe, Ga, Ge, La, Li, Mo, Nb, Ni, Pb, Th, Ti, U, V, W, Y, Zn. For Hg this study does not give definite results. No seasonal differences in moss concentrations from spring to autumn can be shown. PMID:15067476

  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. PMID:24520715

  12. Role of hydrous iron oxide formation in attenuation and diel cycling of dissolved trace metals in a stream affected by acid rock drainage

    USGS Publications Warehouse

    Parker, S.R.; Gammons, C.H.; Jones, C.A.; Nimick, D.A.

    2007-01-01

    Mining-impacted streams have been shown to undergo diel (24-h) fluctuations in concentrations of major and trace elements. Fisher Creek in south-central Montana, USA receives acid rock drainage (ARD) from natural and mining-related sources. A previous diel field study found substantial changes in dissolved metal concentrations at three sites with differing pH regimes during a 24-h period in August 2002. The current work discusses follow-up field sampling of Fisher Creek as well as field and laboratory experiments that examine in greater detail the underlying processes involved in the observed diel concentration changes. The field experiments employed in-stream chambers that were either transparent or opaque to light, filled with stream water and sediment (cobbles coated with hydrous Fe and Al oxides), and placed in the stream to maintain the same temperature. Three sets of laboratory experiments were performed: (1) equilibration of a Cu(II) and Zn(II) containing solution with Fisher Creek stream sediment at pH 6.9 and different temperatures; (2) titration of Fisher Creek water from pH 3.1 to 7 under four different isothermal conditions; and (3) analysis of the effects of temperature on the interaction of an Fe(II) containing solution with Fisher Creek stream sediment under non-oxidizing conditions. Results of these studies are consistent with a model in which Cu, Fe(II), and to a lesser extent Zn, are adsorbed or co-precipitated with hydrous Fe and Al oxides as the pH of Fisher Creek increases from 5.3 to 7.0. The extent of metal attenuation is strongly temperature-dependent, being more pronounced in warm vs. cold water. Furthermore, the sorption/co-precipitation process is shown to be irreversible; once the Cu, Zn, and Fe(II) are removed from solution in warm water, a decrease in temperature does not release the metals back to the water column. ?? 2006 Springer Science+Business Media B.V.

  13. Thiol and metal contents in periphyton exposed to elevated copper and zinc concentrations: a field and microcosm study.

    PubMed

    Le Faucheur, Séverine; Behra, Renata; Sigg, Laura

    2005-10-15

    Phytochelatins are metal-binding polypeptides produced by algae under metal exposure. The aim of this study was to investigate the effects of metal concentration variations in natural systems on periphyton at the biochemical level by analyzing its intracellular thiol content, in particular phytochelatins. To that purpose, two field campaigns were conducted in a stream subject to an increase of dissolved metal concentrations (particularly Cu and Zn) during rain events, which results in an increase of their accumulation in periphyton. At background metal concentrations, several thiols were detectable in periphyton, namely, glutathione (GSH), gamma-glutamylcysteine (gammaGluCys), phytochelatins (PC2), and some unidentified thiols, U1 and U2. Glutathione and gammaGluCys contents were found to vary independently of the rain, as well as U1 and U2, whereas the phytochelatin content increased during the rain events. To investigate whether Cu or Zn may be responsible for this increase, microcosm experiments were carried out with natural water enriched with Cu, Zn, and Cd separately, and Cu and Zn in combination. In this study, GSH, PC2, and U1 were also detected, but not gammaGluCys. An increase in accumulated Cu content did not induce any changes in thiol content, whereas an increase of the Zn content induced a decrease in GSH content and an increase in phytochelatin content. Zinc rather than Cu may thus induce a phytochelatin content increase in periphyton in the field studies. Addition of Cu and Zn in combination also induced an increase in phytochelatin content. Cadmium was found to be the most effective inducer, with the production of larger phytochelatins (PC3-4). This study is the first one to report changes in thiol content in periphyton in response to an increase of the metal concentration in natural freshwaters. PMID:16295881

  14. The role of dissolved organic matter and its adsorption for the fate of heavy metals in clay-rich soil

    NASA Astrophysics Data System (ADS)

    Refaey, Yasser B.; Jansen, Boris; El-Shater, Abdel-Hamid; El-Haddad, Abdel-Aziz; Kalbitz, Karsten

    2014-05-01

    Heavy metals (HMs), due to their toxic and hazardous nature, are possibly the most widespread contaminants imposing a serious threat to human health. To find out the effect of dissolved organic matter (DOM) and soil constituents on the uptake of Cu, Ni, and Zn, batch adsorption experiments were conducted using five soils sampled from Egypt. Sorption data were interpreted in terms of the initial mass (IM) isotherm model. In all soils, for all metals and in all experiments, the majority of the HMs were immobilized on the solid phase. The addition of DOM and timing thereof was found to play a pivotal role in determining the affinity of the HMs for the solid phase. When DOM and HMs were added simultaneously, Cu affinity decreased in Fe-(hydr)oxide rich soils (by 7%) and increased in soils poor in Fe-(hydr)oxide (by 6-10%). When DOM was added first, followed by HMs in a later stage affinity of Cu strongly increased in most soils. In contrast, for both Ni and Zn the affinity to the solid phase was enhanced (3-18%) in presence of DOM regardless of whether the DOM was added simultaneously with or prior to HMs addition. The difference is explained by Cu binding to the solid phase and to DOM through strong inner-sphere complexes, whereas Ni and Zn interacted predominantly through weaker electrostatic interactions. As a result Cu was able to bind more strongly to previously adsorbed DOM on the solid phase in case of smectite, while this effect was counteracted by the coating of available specific binding sites on Fe-(hydr)oxides.

  15. Toxicity identification evaluation of metal-contaminated sediments using an artificial pore water containing dissolved organic carbons

    SciTech Connect

    Boucher, A.M.; Watzin, M.C.

    1999-03-01

    Recent investigations of sediment-associated pollutants in Lake Champlain indicated significant contamination with As, Mn, and Ni in Outer Malletts Bay, Vermont, US. Ceriodaphnia dubia exposed to sediment pore water from several sites in Outer Malletts Bay showed repeatable, acute mortality at only one site. A toxicity identification evaluation (TIE) was conducted on pore water to determine the contaminants causing mortality at this site. Unlike most TIE applications, the dilution water used in these tests was formulated to match the hardness, alkalinity, pH, conductivity, and dissolved organic carbon content of the pore water. Results from phase 1 of the TIE indicated that divalent metals may be responsible for toxicity. Phase 2 results revealed levels of Mn above LC50 values. Spiking experiments employed in phase 3 confirmed Mn as the principal toxicant in sediment pore water. The formulated pore water worked well and helped ensure that toxicant behavior was influenced primarily by each TIE manipulation and not by physical and chemical differences between the dilution and site water. Although the Mn toxicity at this site may be the result of its unique geomorphology, this situation underscores the need to look broadly for potential toxicants when evaluating contaminated sites.

  16. Placental Metal Concentrations in Relation to Maternal and Infant Toenails in a U.S. Cohort.

    PubMed

    Punshon, Tracy; Li, Zhigang; Marsit, Carmen J; Jackson, Brian P; Baker, Emily R; Karagas, Margaret R

    2016-02-01

    Metal contaminants cross the placenta, presenting a heightened risk of perturbing fetal development. Information about placental concentrations and transfer of multiple potentially toxic metals from low to moderate exposure is lacking. We measured concentrations of Cd, Pb, Hg, Mn, Se, and Zn in 750 placentas collected from women enrolled in the New Hampshire Birth Cohort Study and examined the correlation between elements, and profiles of potentially toxic metals (Cd, Pb, Hg, and Mn) stratified by nutrient concentrations (Zn and Se) using principal components analyses. We further examined the indirect effects of maternal metal concentrations on infant metal concentrations through placental metal concentrations using structural equation models. Placental metal concentrations were all correlated, particularly Zn and Mn, and Zn and Cd, and the principal component of metals differed by stratum of high versus low Zn and Se. Associations were observed between placenta and maternal toenail Se (β = 63.49; P < 0.0001) and Pb (β = 0.90; P < 0.0001) but not other metals. Structural equation models did not indicate any statistically significant indirect effects through placental metal concentrations. Placental metal concentrations may represent a distinct biomarker of metal exposure and adverse health impacts to the fetus, particularly those stemming from the placenta. PMID:26727403

  17. Influence of dissolved organic matter and manganese oxides on metal speciation in soil solution: A modelling approach.

    PubMed

    Schneider, Arnaud R; Ponthieu, Marie; Cancès, Benjamin; Conreux, Alexandra; Morvan, Xavier; Gommeaux, Maxime; Marin, Béatrice; Benedetti, Marc F

    2016-06-01

    Trace element (TE) speciation modelling in soil solution is controlled by the assumptions made about the soil solution composition. To evaluate this influence, different assumptions using Visual MINTEQ were tested and compared to measurements of free TE concentrations. The soil column Donnan membrane technique (SC-DMT) was used to estimate the free TE (Cd, Cu, Ni, Pb and Zn) concentrations in six acidic soil solutions. A batch technique using DAX-8 resin was used to fractionate the dissolved organic matter (DOM) into four fractions: humic acids (HA), fulvic acids (FA), hydrophilic acids (Hy) and hydrophobic neutral organic matter (HON). To model TE speciation, particular attention was focused on the hydrous manganese oxides (HMO) and the Hy fraction, ligands not considered in most of the TE speciation modelling studies in soil solution. In this work, the model predictions of free ion activities agree with the experimental results. The knowledge of the FA fraction seems to be very useful, especially in the case of high DOM content, for more accurately representing experimental data. Finally, the role of the manganese oxides and of the Hy fraction on TE speciation was identified and, depending on the physicochemical conditions of the soil solution, should be considered in future studies. PMID:27017138

  18. Carbon and metal concentrations, size distributions and fluxes in major rivers of the Amazon basin

    NASA Astrophysics Data System (ADS)

    Benedetti, Marc F.; Mounier, Stephane; Filizola, Naziano; Benaim, Jean; Seyler, Patrick

    2003-05-01

    The chemical composition of the Amazon River results from the mixing of two water types: black water and white water. On-site fractionation by sequential tangential ultrafiltration (STUF) was used to differentiate transported organic carbon and to determine the distribution and association of major and trace elements with different size fraction of the organic carbon (OC). Several sampling campaigns (1994-1996) allow a monthly quantification of particulate (OCP, MeP), colloidal (OCC, MeC) and dissolved (OCD, MeD) organic carbon and metal ions inputs. In white rivers the OC is mainly concentrated in the low molecular weight fraction (OCD < 5000 D) while in black rivers most of the OC is in the heavier molecular weight fractions (OCP and OCC > 5 kDa). For Mg, Ca and K, 50% of the total amount of each element is found in fraction MeD while 15% and 35% are found in fractions MeC and MeP, respectively. Al and Fe are in the particulate fraction at 99% of the total metal concentration for all river samples. This work emphasizes the coagulation processes and the sink for elements in the mixing zone. These physicochemical transformations of the organic matter vary seasonally. The changes happen during the transition periods: before high-level waters and before low-level waters. By way of flux measurement, a seasonal carbon loss was observed. The estimated annual organic carbon flux of the Amazon at Òbidos is 28 × 106 t. At the same time, an average of 9 × 106 t of organic carbon per year is retained in the reach between Manaus and Òbidos, probably via coagulation processes.

  19. Metal cation/anion adsorption on calcium carbonate: Implications to metal ion concentrations in groundwater

    SciTech Connect

    Zachara, J.M.; Cowan, C.E.; Resch, C.T.

    1990-05-01

    This chapter evaluates the sorption behavior of metallic ions on specimen calcite as a basis for determining the importance of calcite relative to other subsurface sorbents, such as layer silicates and oxides, in controlling metal ion concentration in calcareous groundwaters. A review of the literature shows the sorption of both metallic cations and anions on calcite over ranges in pH and CO{sub 2} partial pressure to be consistent with a surface-exchange process where cations exchange with surface Ca and anions exchange with surface CO{sub 3}. A general surface-exchange model was developed to account for the effects of Ca and CO{sub 3} concentrations, pH, and calcite surface area on cation and anion sorption onto calcite. The model was applied to recently developed experimental sorption data of Zn and SeO{sub 3} on specimen calcite in equilibrium CaCO{sub 3}(aq) suspensions. The surface-exchange model was able to describe the effects of pH on both cation and anion sorption, and provided good predictions of the effects of variable CO{sub 2}(g) pressure on Zn sorption and of PO{sub 4} on SeO{sub 3} sorption. The surface-exchange model, combined with sorption constants for other phases, was used to calculate Cd sorption to a hypothetical aquifer material containing a mixture of sorbents. The sorbent concentrations were fixed to those expected in groundwater zones. The multi-sorbent calculation documented the importance of calcite as a sorbent for metallic ions in groundwater.93 refs., 18 figs., 5 tabs.

  20. Blood metals concentration in type 1 and type 2 diabetics.

    PubMed

    Forte, Giovanni; Bocca, Beatrice; Peruzzu, Angela; Tolu, Francesco; Asara, Yolande; Farace, Cristiano; Oggiano, Riccardo; Madeddu, Roberto

    2013-12-01

    Mechanisms for the onset of diabetes and the development of diabetic complications remain under extensive investigations. One of these mechanisms is abnormal homeostasis of metals, as either deficiency or excess of metals, can contribute to certain diabetic outcomes. Therefore, this paper will report the blood levels of chromium (Cr), copper (Cu), iron (Fe), manganese (Mn), mercury (Hg), nickel (Ni), lead (Pb), selenium (Se), and zinc (Zn) in subjects with type 1 diabetes (n = 192, mean age 48.8 years, mean disease duration 20.6 years), type 2 diabetes (n = 68, mean age 68.4 years, mean disease duration 10.2 years), and in control subjects (n = 59, mean age 57.2 years), and discuss the results indicating their possible role in diabetes. The metal concentrations were measured by sector field inductively coupled plasma mass spectrometry after microwave-induced acid digestion of blood samples. The accuracy was checked using a blood-based certified reference material, and recoveries of all elements were in the range of 92-101 % of certified values. Type 1 diabetes was found to be associated with Cr (p = 0.02), Mn (p < 0.001), Ni (p < 0.001), Pb (p = 0.02), and Zn (p < 0.001) deficiency, and type 2 diabetes with Cr (p = 0.014), Mn (p < 0.001), and Ni (p < 0.001) deficiency. These deficiencies were appreciated also subdividing the understudied patients for gender and age groups. Furthermore, in type 1 diabetes, there was a positive correlation between Pb and age (p < 0.001, ρ = 0.400) and Pb and BMI (p < 0.001, ρ = 0.309), while a negative correlation between Fe and age (p = 0.002, ρ = -0.218). In type 2 diabetes, there was a negative correlation between Fe and age (p = 0.017, ρ = -0.294) and Fe and BMI (p = 0.026, ρ = -0.301). Thus, these elements may play a role in both forms of diabetes and combined mineral supplementations could have beneficial effects. PMID:24222606

  1. Predicting the toxicity of sediment-associated trace metals with simultaneously extracted trace metal: Acid-volatile sulfide concentrations and dry weight-normalized concentrations: A critical comparison

    USGS Publications Warehouse

    Long, E.R.; MacDonald, D.D.; Cubbage, J.C.; Ingersoll, C.G.

    1998-01-01

    The relative abilities of sediment concentrations of simultaneously extracted trace metal: acid-volatile sulfide (SEM:AVS) and dry weight- normalized trace metals to correctly predict both toxicity and nontoxicity were compared by analysis of 77 field-collected samples. Relative to the SEM:AVS concentrations, sediment guidelines based upon dry weight-normalized concentrations were equally or slightly more accurate in predicting both nontoxic and toxic results in laboratory tests.

  2. Influence of domestic pets on soil concentrations of dissolved organic carbon, nitrogen, and phosphorus under turfgrass in apartment complexes of Central Texas, USA

    NASA Astrophysics Data System (ADS)

    Steele, M.; Aitkenhead-Peterson, J. A.

    2009-12-01

    High nitrogen (N) and phosphorus (P) watershed loading rates increases the concentration 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 concentrations 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 concentrations of soil dissolved 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 dissolved nitrogen (TDN), nitrate-N, ammonium-N, dissolved organic N, and orthophosphate-P. Results indicated significantly increased concentrations 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 concentrations of orthophosphate-P at both locations. Baker, L.A., D. Hope, Y. Xu, et al. 2001. Nitrogen balance for the central Arizona

  3. Influence of pH, hardness, dissolved organic carbon concentration, and dissolved organic matter source on the acute toxicity of copper to Daphnia magna in soft waters: implications for the biotic ligand model.

    PubMed

    Ryan, Adam C; Tomasso, Joseph R; Klaine, Stephen J

    2009-08-01

    The influence of pH, dissolved organic carbon (DOC) concentration, water hardness, and dissolved organic matter (DOM) source on the acute toxicity of copper were investigated with standardized 48-h Daphnia magna toxicity tests. Toxicity tests were conducted according to a four-factor complete factorial design. Nominal factor levels were as follows: pH 6 and 8; DOC, 2.5 and 10 mg/L; hardness, 10, 20, and 40 mg/L as CaCO3; and two DOM sources (collected from the Black River and Edisto River, SC, USA). The experimental design resulted in 24 different factor level combinations. Results indicated that all factors had significant effects on copper toxicity. Furthermore, a strong interactive effect of DOC concentration and pH was detected. Because the biotic ligand model (BLM) has become a widely used tool for predicting toxicity and interpreting toxicity test results, its performance with these data was evaluated. Seventy percent of BLM predictions were within twofold of the observed median lethal concentrations. However, BLM parameters could be adjusted to improve model performance with this data set. This analysis suggested that in soft waters, the CuOH+ complex binds more strongly with the biotic ligand and that the competitive effect of hardness cations should be increased. The results of the present study may have implications for application of the BLM to some types of surface waters. Furthermore, a comprehensive analysis of BLM performance with all available data should be performed, and necessary updates to model parameters should be made to produce the most robust and widely applicable model. PMID:19265455

  4. Reusable chelating resins concentrate metal ions from highly dilute solutions

    NASA Technical Reports Server (NTRS)

    Bauman, A. J.; Weetal, H. H.; Weliky, N.

    1966-01-01

    Column chromatographic method uses new metal chelating resins for recovering heavy-metal ions from highly dilute solutions. The absorbed heavy-metal cations may be removed from the chelating resins by acid or base washes. The resins are reusable after the washes are completed.

  5. An extensive study of the concentrations of particulate/dissolved radiocaesium derived from the Fukushima Dai-ichi Nuclear Power Plant accident in various river systems and their relationship with catchment inventory.

    PubMed

    Yoshimura, Kazuya; Onda, Yuichi; Sakaguchi, Aya; Yamamoto, Masayoshi; Matsuura, Yuki

    2015-01-01

    An extensive investigation of particulate radiocaesium in suspended solids and dissolved radiocaesium in river water was undertaken at 30 sites in Fukushima and Miyagi Prefectures in December 2012, and their relationships with catchment inventory and the solid/liquid distribution coefficient (Kd) were evaluated. Rivers located in the coastal region on the north side of the Fukushima Dai-ichi Nuclear Power Plant exhibited relatively higher particulate radiocaesium concentrations. Significant correlations were found between concentrations of particulate/dissolved radiocaesium and average catchment inventories, indicating that the concentrations of particulate/dissolved radiocaesium could be approximated from the catchment inventory. Particulate radiocaesium concentration was significantly correlated with dissolved radiocaesium concentration (with the exception of concentrations measured in estuaries), and the geometric mean Kd was calculated as 3.6 × 10(5) with a 95% confidence interval of 2.6-5.1 × 10(5). PMID:25242014

  6. Metal concentrations in demersal fish species from Santa Maria Bay, Baja California Sur, Mexico (Pacific coast).

    PubMed

    Jonathan, M P; Aurioles-Gamboa, David; Villegas, Lorena Elizabeth Campos; Bohórquez-Herrera, Jimena; Hernández-Camacho, Claudia J; Sujitha, S B

    2015-10-15

    Concentrations of 11 trace metals (Fe, Mn, Cr, Cu, Ni, Co, Pb, Zn, Cd, As, Hg) in 40 fish species from Santa Maria Bay, Baja California Sur, Mexico, the strategically important area for marine mammals and organisms were analyzed. Based on their concentrations the ranking of metals Fe>Zn>Ni>Cr>Mn>Pb>Cu>Co>As>Cd>Hg suggests that organism size, metabolism and feeding habits are correlated with metal concentrations. Local geological formations affect the concentrations of different metals in the aquatic environment and are subsequently transferred to fishes. The correlation analysis suggests that metabolism and nurturing habits impact the concentration of metals. Concentrations of Fe and Mn appear to be influenced by scavenging and absorption processes, which vary by species. The considerable variability in the metal concentrations obtained in different species underscores the importance of regular monitoring. PMID:26228068

  7. 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 M.

    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

  8. Influence of acid volatile sulfide and metal concentrations on metal bioavailability to marine invertebrates in contaminated sediments

    USGS Publications Warehouse

    Lee, B.-G.; Lee, J.-S.; Luoma, S.N.; Choi, H.J.; Koh, C.-H.

    2000-01-01

    An 18-day microcosm study was conducted to evaluate the influence of acid volatile sulfides (AVS) and metal additions on bioaccumulation from sediments of Cd, Ni, and Zn in two clams (Macoma balthica and Potamocorbula amurensis) and three marine polychaetes (Neanthes arenaceodentata, Heteromastus filiformis, and Spiophanes missionensis). Manipulation of AVS by oxidation of naturally anoxic sediments allowed use of metal concentrations typical of nature and evaluation of processes important to chronic metal exposure. A vertical sediment column similar to that often found in nature was used to facilitate realistic biological behavior. Results showed that AVS or porewater (PW) metals controlled bioaccumulation in only 2 of 15 metal-animal combinations. Bioaccumulation of all three metals by the bivalves was related significantly to metal concentrations extracted from sediments (SEM) but not to [SEM - AVS] or PW metals. SEM predominantly influenced bioaccumulation of Ni and Zn in N. arenaceodentata, but Cd bioaccumulation followed PW Cd concentrations. SEM controlled tissue concentrations of all three metals in H. filiformis and S. missionensis, with minor influences from metal-sulfide chemistry. Significant bioaccumulation occurred when SEM was only a small fraction of AVS in several treatments. Three factors appeared to contribute to the differences between these bioaccumulation results and the results from toxicity tests reported previously: differences in experimental design, dietary uptake, and biological attributes of the species, including mode and depth of feeding.An 18-day microcosm study was conducted to evaluate the influence of acid volatile sulfides (AVS) and metal additions on bioaccumulation from sediments of Cd, Ni, and Zn in two clams (Macoma balthica and Potamocorbula amurensis) and three marine polychaetes (Neanthes arenaceodentata, Heteromastus filiformis, and Spiophanes missionensis). Manipulation of AVS by oxidation of naturally anoxic sediments

  9. Metal concentrations in Hydrocynus vittatus (Castelnau 1861) populations from a premier conservation area: Relationships with environmental concentrations.

    PubMed

    Gerber, Ruan; Smit, Nico J; van Vuren, Johan H J; Wepener, Victor

    2016-07-01

    Metals are known to have deleterious effects on aquatic ecosystems, so monitoring the bioaccumulation of these pollutants is important for the assessment of potential impacts. The aim of the study was therefore to determine the degree to which aquatic biota in selected rivers of the world renowned Kruger National Park (KNP) are exposed to metals entering from the catchments outside the KNP and to determine how these metal levels reflect what is occurring within the environment. Many of these rivers have never previously been assessed and those which have, have not been assessed within the past two decades. Tigerfish (Hydrocynus vittatus) is an economically important apex predator and was selected as the bioindicator for this study. Fish were sampled from the KNP sections of the Luvuvhu, Letaba and Olifants Rivers during the high and low flow periods from 2009 to 2011. The analysis of various metals from the aforementioned systems revealed spatial and temporal related variation in metal level patterns of the chosen bioindicator, with concentrations in fish from the Olifants River>Letaba River>Luvuvhu River and 2009>2010>2011. Although there were differences between rivers, metal concentrations were comparable and indicate that all of the studied KNP rivers, even those considered to be in a natural state are affected to some degree by anthropogenic activities. However, concentrations found during this study were much lower than previous studies in the area, as well as contaminated sites across the world, but were higher than concentrations in fish from contaminated sites in the Vaal River, South Africa. Bioaccumulated metals showed no correlation to metals in the water column, but some were correlated to sediment metal concentrations and the contamination and bioavailability of these metals within the sediments. This is of concern when managing the water resources of the conservation area since the contaminants enter the park from outside the borders and pose

  10. Concentrations of total dissolved organic carbon and humic and hydrophilic sub-fractions extracted from major Dutch soil types and their relation with soil properties

    NASA Astrophysics Data System (ADS)

    Comans, Rob N. J.; van Zomeren, Andre; Groenenberg, Jan E.

    2013-04-01

    Measurements of the concentrations of dissolved organic carbon (DOC) and its humic and hydrophilic sub-fractions in different soil types, and our understanding of the underlying processes, are still limited. This knowledge gap strongly hampers adequate modelling of the speciation, mobility and bioavailability of trace elements in soils, the reactive DOC concentration being a major controlling parameter, as well as assessments of carbon cycling between soil and water. In this study, we have analysed the concentration of DOC and its humic and hydrophilic sub-fractions in 10-3M CaCl2 extractions of approximately 100 top- and sub-soil samples from major Dutch soil types (sand, peat and clay). A rapid batch fractionation procedure (van Zomeren & Comans, 2007) was used to distinguish the concentrations of dissolved humic acids (HA), fulvic acids (FA), hydrophobic neutrals (HON) and hydrophilic acids (Hy). Field-moist samples were used, as well as dried samples from the archive of samples collected for the realisation of the recently published geochemical soil atlas of The Netherlands (Mol et al., 2012). The latter samples have been incubated for one month, after being re-moisturised to field capacity, prior to the extraction and fractionation procedure, in order to limit previously observed effects of soil-drying on DOC concentration and composition. Substantial differences in the concentration and composition of DOC between dried, re-moisturised and field-moist samples were indeed observed and will be discussed. In addition, and as a first step towards a model for the partitioning of DOC and its humic sub-fractions, empirical partition functions have been derived, which relate their dissolved concentrations to potentially controlling soil properties such as pH, total soil organic matter (SOM) and the reactive surface area of iron- and aluminium(hydr)oxides, as estimated from selective extractions. The resulting empirical functions are discussed in light of current

  11. Metal accumulation and metallothionein concentrations in tree swallow nestlings near acidified lakes

    SciTech Connect

    St. Louis, V.; Breebaart, L. . Dept. of Zoology); Barlow, J.C. . Dept. of Zoology Royal Ontario Museum, Toronto, Ontario . Dept. of Ornithology); Klaverkamp, J.F. . Dept. of Fisheries and Oceans)

    1993-07-01

    The authors studied metal accumulation in hepatic and renal tissues of tree swallow (Tachycineta bicolor) nestlings at acidified and nonacid reference lakes in northwestern Ontario. Hepatic concentrations of metallothionein (metal-binding proteins, MT) in tree swallow nestlings were negatively correlated with pH of the nest-site lake. Combined concentrations of Cu and Zn in the liver were correlated with liver MT concentrations, but Cd was not. Although no overt signs of metal toxicity were observed in nestlings near acid lakes, the results clearly provided evidence that metals are transferred from acid lakes to birds and that these metals are correlated with increases in hepatic MT production.

  12. Passive treatment of acid mine drainage with high metal concentrations using dispersed alkaline substrate.

    PubMed

    Rötting, Tobias S; Thomas, Robert C; Ayora, Carlos; Carrera, Jesús

    2008-01-01

    Passive treatment systems based on the dissolution of coarse calcite grains are widely used to remediate acid mine drainage (AMD). Unfortunately, they tolerate only low metal concentrations or acidity loads, because they are prone to passivation (loss of reactivity due to coating) and/or clogging (loss of permeability) by precipitates. To overcome these problems, a dispersed alkaline substrate (DAS) composed of a fine-grained alkaline reagent (calcite sand) mixed with a coarse inert matrix (wood chips) was developed. The small grains provide a large reactive surface and dissolve almost completely before the growing layer of precipitates passivates the substrate, whereas the dispersion of nuclei for precipitation on the inert surfaces retards clogging. Chemical and hydraulic performance of DAS was investigated in two laboratory columns fed at different flow rates with natural AMD of pH 2.3 to 3.5 and inflow net acidity 1350 to 2300 mg/L as CaCO(3). The DAS columns removed 900 to 1600 mg/L net acidity, 3 to 4.5 times more than conventional passive treatment systems. Regardless of the flow rate employed, Al, Fe(III), Cu, and Pb were virtually eliminated. Minor Zn, Ni, and Cd were removed at low flow rates. High acidity removal is possible because these metals accumulate intentionally in DAS, and their precipitation promotes further calcite dissolution. During 15 mo, DAS operated without clogging at 120 g acidity/m(2).d, four times the loading rate recommended for conventional passive systems; DAS may therefore be capable of treating AMD at sites where influent chemistry precludes the use of other passive systems. PMID:18689735

  13. Heavy metal concentrations in earthworms from soil amended with sewage sludge

    USGS Publications Warehouse

    Beyer, W.N.; Chaney, R.L.; Mulhern, B.M.

    1982-01-01

    Metal concentrations in soil may be elevated considerably when metal-laden sewage sludge is spread on land. Metals in earthworms (Lumbricidae) from agricultural fields amended with sewage sludge and from experimental plots were examined to determine if earthworms are important in transferring metals in soil to wildlife. Earthworms from four sites amended with sludge contained significantly (P . < 0.05) more Cd (12 times), Cu (2.4 times), Zn (2.0 times), and Pb (1.2 times) than did earthworms from control sites, but the concentrations detected varied greatly and depended on the particular sludge application. Generally, Cd and Zn were concentrated by earthworms relative to soil, and Cu, Pb, and Ni were not concentrated. Concentrations of Cd, Zn, Cu, and Pb in earthworms were correlated (P < 0.05) with those in soil. The ratio of the concentration of metals in earthworms to the concentration of metals in soil tended to be lower in contaminated soil than in clean soil. Concentrations of Cd as high as 100 ppm (dry wt) were detected in earthworms from soil containing only 2 ppm Cd. These concentrations are considered hazardous to wildlife that eat worms. Liming soil decreased Cd concentrations in earthworms slightly (P < 0.05) but had no discernible effect on concentrations of the other metals studied. High Zn concentrations in soil substantially reduced Cd concentrations in earthworms.

  14. Heavy metal concentrations in earthworms from soil amended with sewage slude

    SciTech Connect

    Beyer, W.N.; Chaney, R.L.; Mulhern, B.M.

    1982-07-01

    Metal concentrations in soil may be elevated considerably when metal-laden sewage sludge is spread on land. Metals in earthworms (Lumbricidae) from agicultural fields amended with sewage sludge and from experimental plots were examined to determine if earthworms are important in transferring metals in soil to wildlife. Earthworms from four sites amended with sludge contained significantly (P<0.05) more Cd (12 times), Cu (2.4 times), Zn (2.0 times), and Pb (1.2 times) than did earthworms from control sites, but the concentrations detected varied greatly and depended on the particular sludge application. Generally, Cd and Zn were concentrated by earthworms relative to soil, and Cu, Pb, and Ni were not concentrated. Concentrations of Cd, Zn, Cu, and Pb in earthworms were correlated (P<0.05) with those in soil. The ratio of the concentration of metals in earthworms to the concentration of metals in soil tended to be lower in contaminated soil than in clean soil. Concentrations of Cd as high as 100 ppm (dry wt) were detected in earthworms from soil containing only 2 ppm Cd. These concentrations are considered hazardous to wildlife that eat worms. Liming soil decreased Cd concentrations in earthworms slightly (P<0.05) but had no discernible effect on concentrations of the other metals studied. High Zn concentrations in soil substantially reduced Cd concentrations in earthworms.

  15. A Synthesis of Light Absorption Properties of the Arctic Ocean: Application to Semi-analytical Estimates of Dissolved Organic Carbon Concentrations from Space

    NASA Technical Reports Server (NTRS)

    Matsuoka, A.; Babin, M.; Doxaran, D.; Hooker, S. B.; Mitchell, B. G.; Belanger, S.; Bricaud, A.

    2014-01-01

    The light absorption coefficients of particulate and dissolved 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 concentration of colored dissolved organic matter (CDOM) in watersheds on the Siberian 76 side, which contains a large amount of dissolved organic carbon (DOC) compared to waters off 77 North America. In contrast, the relationship between the phytoplankton absorption (a()) and chlorophyll a (chl a) concentration 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 concentrations for coastal waters at the Pan-Arctic scale is presented and applied to satellite ocean color data.

  16. A novel method of non-violent dissolution of sodium metal in a concentrated aqueous solution of Epsom salt

    NASA Astrophysics Data System (ADS)

    Lakshmanan, A. R.; Prasad, M. V. R.; Ponraju, D.; Krishnan, H.

    2004-10-01

    A new technique of non-violent and fast dissolution of sodium metal in a concentrated aqueous solution of Epsom salt (MgSO4.7H2O) at room temperature (RT) has been developed. The dissolution process is mildly exothermic but could be carried out even in a glass beaker in air under swift stirring condition. The reaction products consist of mixed salts of MgSO4 and Na2SO4 as well as Mg(OH)2 which are only mildly alkaline and hence are non-corrosive and non-hazardous unlike NaOH. A 50 mL solution having Epsom salt concentration of 2 M was found to give the optimal composition for disposal of 1 g of sodium. Supersaturated (>2.7 M), as well as dilute (<1.1 M) solutions, however, cause violent reactions and hence should be avoided. Repeated sodium dissolution in Epsom solution produced a solid waste of 4.7 g per g of sodium dissolved which is comparable with the waste (4 g) produced in 8 M NaOH solution. A 1.4 M Epsom solution sprayed with a high-pressure jet cleaner at RT in air easily removed the sodium blocked inside a metal pipe made of mild steel. The above jet also dissolved peacefully residual sodium collected on the metal tray after a sodium fire experiment. No sodium fire or explosion was observed during this campaign. The Epsom solution spray effectively neutralized the minor quantity of sodium aerosol produced during this campaign. This novel technique would hence be quite useful for draining sodium from fast breeder reactor components and bulk processing of sodium as well as for sodium fire fighting.

  17. Water Temperature, Specific Conductance, pH, and Dissolved-Oxygen Concentrations in the Lower White River and the Puyallup River Estuary, Washington, August-October 2002

    USGS Publications Warehouse

    Ebbert, James C.

    2003-01-01

    The U.S. Geological Survey, Washington State Department of Ecology, and Puyallup Tribe of Indians monitored water temperature, specific conductance, pH, and dissolved-oxygen concentrations 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 21.1oC (degrees Celsius) at river mile 4.9 and 19.6oC at river mile 1.8 exceeded the water-quality standard of 18oC 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. Dissolved-oxygen concentrations 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 dissolved-oxygen concentrations. The lowest concentration of dissolved oxygen observed was 7.9 mg/L (milligrams per liter) at river mile 1.8. The

  18. Background concentrations of metals in soils from selected regions in the State of Washington

    USGS Publications Warehouse

    Ames, K.C.; Prych, E.A.

    1995-01-01

    Soil samples from 60 sites in the State of Washington were collected and analyzed to determine the magnitude and variability of background concen- trations of metals in soils of the State. Samples were collected in areas that were relatively undisturbed by human activity from the most pre- dominant soils in 12 different regions that are representative of large areas of Washington State. Concentrations of metals were determined by five different laboratory methods. Concentrations of mercury and nickel determined by both the total and total-recoverable methods displayed the greatest variability, followed by chromium and copper determined by the total-recoverable method. Concentrations of other metals, such as aluminum and barium determined by the total method, varied less. Most metals concentrations were found to be more nearly log-normally than normally distributed. Total metals concentrations were not significantly different among the different regions. However, total-recoverable metals concentrations were not as similar among different regions. Cluster analysis revealed that sampling sites in three regions encompassing the Puget Sound could be regrouped to form two new regions and sites in three regions in south-central and southeastern Washington State could also be regrouped into two new regions. Concentrations for 7 of 11 total-recoverable metals correlated with total metals concentrations. Concen- trations of six total metals also correlated positively with organic carbon. Total-recoverable metals concentrations did not correlate with either organic carbon or particle size. Concentrations of metals determined by the leaching methods did not correlate with total or total-recoverable metals concentrations, nor did they correlate with organic carbon or particle size.

  19. Maternal exposure to alkali, alkali earth, transition and other metals: Concentrations and predictors of exposure.

    PubMed

    Hinwood, A L; Stasinska, A; Callan, A C; Heyworth, J; Ramalingam, M; Boyce, M; McCafferty, P; Odland, J Ø

    2015-09-01

    Most studies of metals exposure focus on the heavy metals. There are many other metals (the transition, alkali and alkaline earth metals in particular) in common use in electronics, defense industries, emitted via combustion and which are naturally present in the environment, that have received limited attention in terms of human exposure. We analysed samples of whole blood (172), urine (173) and drinking water (172) for antimony, beryllium, bismuth, cesium, gallium, rubidium, silver, strontium, thallium, thorium and vanadium using ICPMS. In general most metals concentrations were low and below the analytical limit of detection with some high concentrations observed. Few factors examined in regression models were shown to influence biological metals concentrations and explained little of the variation. Further study is required to establish the source of metals exposures at the high end of the ranges of concentrations measured and the potential for any adverse health impacts in children. PMID:25984984

  20. 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

  1. Metal concentrations in aquatic macrophytes as influenced by soil and acidification

    USGS Publications Warehouse

    Sparling, D.W.; Lowe, T.P.

    1998-01-01

    Bioavailability of metals to aquatic plants is dependent on many factors including ambient metal concentration, pH of soil or water, concentration of ligands, competition with other metals for binding sites, and mode of exposure. Plants may be exposed to metals through water, air, or soil, depending on growth form. This paper examines the influence of soil type under two regimens of water acidification on metal uptake by four species of aquatic macrophytes: smartweed (Polygonum sagittatum), burreed (Sparganium americanum), pondweed (Potamogeton diversifolius), and bladderwort (Utricularia vulgaris) in constructed, experimentally acidified wetlands. Soil types consisted of a comparatively high-metal clay or a lower-metal sandy loam. Each pond was either acidified to pH ca. 4.85.3 or allowed to remain circumneutral. Metal concentrations tended to be higher in the submerged bladderwort and pondweed than in the emergent burreed and smartweed. Soils were important to plant metal concentrations in all species, but especially in the emergents. Acidification influenced plant concentrations of some metals and was especially important in the submerged pondweed. Bioaccumulation of metals occurred for Mn, B, Sr, Ba, and Zn, compared to soil concentrations.

  2. Influence of discharge and urbanization on the concentration, speciation, and bioavailability of trace metals in the Raritan River, New Jersey. Final report

    SciTech Connect

    McLaughlin, F.B.; Ashley, G.M.; Renwick, W.H.

    1988-01-01

    The Raritan River and its tributaries are a vital drinking water and recreational resource in central New Jersey. These waters also serve as disposal media for municipal and industrial wastes and urban stormwater runoff. Rapid development over the last several decades has intensified the pressures on the quality and use of Raritan waters. The concentration and speciation of ten trace metals (Ag, As, Cd, Co, Cr, Cu, Hg, Ni, Pb, Zn) were investigated in the Raritan Basin. From September 1985 to April 1987, one hundred twenty depth-integrated samples were collected at four locations and analyzed by Direct-Current Plasma Atomic Emission Spectrometry for concentrations of dissolved, particulate-associated, total, and suspended sediment trace metals. The concentrations of trace metals readily available, potentially available, and not available to aquatic and terrestrial biota are also reported. Discharge is the most important factor influencing the concentration and speciation of trace metals in the Raritan River and its tributaries. Seasonal variations affect speciation patterns, but have a minor impact on concentration and availability to biota. The sub-basin draining a more-urbanized area in the Raritan Basin appeared to have elevated concentrations and increased biological availability of trace metals relative to less-urbanized basins.

  3. 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. PMID:27010168

  4. Concentration and flux of total and dissolved phosphorus, total nitrogen, chloride, and total suspended solids for monitored tributaries of Lake Champlain, 1990-2012

    USGS Publications Warehouse

    Medalie, Laura

    2014-01-01

    Annual and daily concentrations and fluxes of total and dissolved 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 concentration 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 dissolved 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.

  5. [Comparison on concentrations and quality of dissolved organic matter in throughfall and stemflow in a secondary forest of Castanopsis carlesii and Cunninghamia lanceolata plantation].

    PubMed

    Lü, Mao-Kui; Xie, Jin-Sheng; Jiang, Miao-Hua; Luo, Shui-Jin; Zeng, Shao-Juan; Ji, Shu-Rong; Wan, Jing-Juan; Yang, Yu-Sheng

    2014-08-01

    In this paper, monthly variation of dissolved organic matter (DOM) concentrations as well as humification and aromaticity indices in throughfall and stemflow from secondary broadleaved Castanopsis carlesii (BF) forest and Cunninghamia lanceolata plantation (CP) were measured. The DOC concentrations in throughfall were significantly higher with greater variation in BF than in CP. The concentrations of DOC in throughfall were averagely 7.2 and 3.2 times of those in rainfall in BF and CP forests, respectively. The DOC concentrations of stemflow in CP were averagely 2.5 times as much as those in BF, and the DOC concentrations in stemflow tended to be greater in dry season than in rain season for the two forests. A significantly negative relationship was' found between the DOC concentrations in stemflow and the amounts of stemflow for both BF and CP. Moreover, the humification and aromaticity indices of DOM in throughfall in BF was significantly greater than in CP. In contrast, the humification and aromaticity indices of DOM from stemflow of CP were significantly greater than those of BF. This result indicated that the structure of DOM from throughfall was more complex in BF than in CP, and the structure of DOM from stemflow was vice versa. These results indicated that DOM in stemflow and throughfall showed significant variations in quantity and quality between BF and CP and may greatly impact the accumulation of soil organic carbon. PMID:25509068

  6. Heavy metal concentrations and biomarkers of oxidative stress in native mussels (Mytilus edulis chilensis) from Beagle Channel coast (Tierra del Fuego, Argentina).

    PubMed

    Duarte, Claudia A; Giarratano, Erica; Amin, Oscar A; Comoglio, Laura I

    2011-08-01

    The aim of this study was to evaluate the usefulness of oxidative stress biomarkers of pollution in native mussels Mytilus edulis chilensis from the Beagle Channel. Spatial and seasonal variations of catalase, glutathione-S-transferase and lipid peroxidation in gills and digestive gland were analyzed in relation to environmental parameters, heavy metals in sediment and in tissue. Four sites with anthropogenic impact and a control site were selected and monitored during the four seasons of 2007. We found significant differences among sites in concentrations of dissolved nutrients and heavy metals in sediments, with the highest values recorded at sites with anthropogenic pressure. Different patterns were observed between concentrations of metals in tissues and in sediments suggesting differences in bioavailability. There were also significant differences in biomarker responses among sites, despite the strong seasonal variability. Our results showed relatively moderate levels of pollution in the study area as a result of urban influences. PMID:21704346

  7. pH : a key control of the nature and distribution of dissolved organic matter and associated trace metals in soil

    NASA Astrophysics Data System (ADS)

    Pédrot, M.; Dia, A.; Davranche, M.

    2009-04-01

    Dissolved organic matter is ubiquitous at the Earth's surface and plays a prominent role in controlling metal speciation and mobility from soils to hydrosystems. Humic substances (HS) are usually considered to be the most reactive fraction of organic matter. Humic substances are relatively small and formed by chemically diverse organic molecules, bearing different functional groups that act as binding sites for cations and mineral surfaces. Among the different environmental physicochemical parameters controlling the metal speciation, pH is likely to be the most important one. Indeed, pH affect the dissociation of functional groups, and thus can influence the HS structure, their ability to complex metals, their solubility degree allowing the formation of aggregates at the mineral surface. In this context, soil/water interactions conducted through batch system experiments, were carried out with a wetland organic-rich soil to investigate the effect of pH on the release of dissolved organic carbon (DOC) and associated trace elements. The pH was regulated between 4 and 7.5 using an automatic pH stat titrator. Ultrafiltration experiments were performed to separate the dissolved organic pool following decreasing pore sizes (30 kDa, 5 kDa and 2 kDa with 1 Da = 1 g.mol-1). The pH increase induced a significant DOC release, especially in heavy organic molecules (size >5 kDa) with a high aromaticity (>30 %). These were probably humic acids (HA). This HA release influenced (i) directly the trace element concentrations in soil solution since HA were enriched in several trace elements such as Th, REE, Y, U, Cr and Cu; and (ii) indirectly by the breaking of clay-humic complexes releasing Fe- and Al-rich nanoparticles associated with V, Pb and Ti. By contrast, at acid pH, most HS were complexed onto mineral surfaces. They also sequestered iron nanoparticles. Therefore, at low pH, most part of DOC molecules had a size < 5 kDa and lower aromaticity. Thus, the DOC was mostly composed

  8. Distributions of dissolved and particulate biogenic thiols in the subartic Pacific Ocean

    NASA Astrophysics Data System (ADS)

    Dupont, Christopher L.; Moffett, James. W.; Bidigare, Robert R.; Ahner, Beth A.

    2006-12-01

    Dissolved and particulate concentrations of the biogenic thiols cysteine (Cys), arginine-cysteine (Arg-Cys), glutamine-cysteine (Gln-Cys), γ-glutamate-cysteine ( γ-Glu-Cys) and glutathione (GSH) were measured in the subartic Pacific Ocean in the summer of 2003 using high performance liquid chromatography (HPLC) with precolumn derivatization as reported in previous work. In this study, a preconcentration protocol for the derivatized thiols was utilized to extend detection limits of dissolved thiols to picomolar levels. The measured concentrations of particulate and dissolved thiols were uncoupled, with distinctive depth profiles and large differences in the particulate to dissolved ratios between individual compounds. Glutathione was the most abundant particulate thiol whereas the most abundant dissolved thiol was γ-Glu-Cys, with concentrations as high as 15 nM. Given the relatively small pool of intracellular γ-Glu-Cys and the very low dissolved concentrations of GSH, we hypothesize that glutathione released from cells is rapidly converted to the potentially degradation resistant γ-Glu-Cys outside the cell. The relatively high concentrations of other dissolved thiols compared to particulate concentrations implies both biological exudation and slow degradation rates. Some thiols appear to vary with changes in nutrient availability but this effect is difficult to decouple from changes in community structure inferred from pigment analyses. Dissolved thiol concentrations also exceed typical metal concentrations in the subartic Pacific, supporting previous arguments that they may be important in metal speciation.

  9. Metal dynamics and tolerance of Typha domingensis exposed to high concentrations of Cr, Ni and Zn.

    PubMed

    Mufarrege, M M; Hadad, H R; Di Luca, G A; Maine, M A

    2014-07-01

    Typha domingensis was exposed to a 100mgL(-1) Cr+100mgL(-1) Ni+100mgL(-1) Zn solution. Metal tolerance and metal accumulation in plant tissues and sediment were studied over time. Although removal rates were different, the three metals were efficiently removed from water. Leaf and root tissues showed high metal concentration. However, the sediment showed the highest accumulation. During the first hours of contact, metals were not only accumulated by sediment and roots but they were also taken up by the leaves in direct contact with the solution. Over time, metals were translocated from roots to leaves and vice versa. Metals caused growth inhibition and a decrease in chlorophyll concentration and affected anatomical parameters. Despite these sub-lethal effects, T. domingensis demonstrated that it could accumulate Cr, Ni and Zn efficiently and survive an accidental dump of high concentrations of contaminants in systems such as natural and constructed wetlands. PMID:24793518

  10. Heavy metal concentrations in marine fishes collected from fish culture sites in Hong Kong.

    PubMed

    Wong, C K; Wong, P P; Chu, L M

    2001-01-01

    The levels of six heavy metals (Cd, Cr, Cu, Ni, Pb, and Zn) in different tissues of three species of cultured marine fishes (Epinephelus areolatus, Lutjanus russelli, and Sparus sarba) collected from three fish culture sites in Hong Kong were evaluated. Metal pollution problems in the fish culture sites were serious, as reflected by the high metal concentrations recorded in sea water, sediments, and the biomonitor Perna viridis. In general, tissues of all three species contained high concentrations of Zn and Cu, but much lower concentrations of Ni, Pb, Cd, and Cr. Similar pattern of heavy metal concentrations was observed in sea water, sediment, and P. viridis. Metal concentrations in various tissues varied greatly among species and among fish culture sites. Different tissues showed different capacity for accumulating heavy metals. Gonad of all three species contained high concentrations of Zn. On the other hand, liver seemed to be the primary organ for Cu accumulation. Overall, metal concentrations in the tissues of culture marine fishes were much lower than those in P. viridis. Despite high metal levels in sea water and sediments, concentrations of Cd, Cr, and Pb in edible tissues, including muscle and skin, did not exceed permissible levels recommended by the Hong Kong Government for human consumption. PMID:11116341

  11. Kinks in experimental diffusion profiles of a dissolving semi-crystalline polymer explained by a concentration-dependent diffusion coefficient.

    PubMed

    Hermes, Helen E; Sitta, Christoph E; Schillinger, Burkhard; Löwen, Hartmut; Egelhaaf, Stefan U

    2015-06-28

    The dissolution of polyethylene oxide (PEO) tablets in water has been followed in situ by neutron radiography. When in contact with water, the crystalline phase of semi-crystalline PEO melts once a certain water content is attained. Polymer concentration profiles obtained from the neutron transmission images exhibited a pronounced kink which corresponds to a sharp front in the images and which is related to the melting transition. Sharp diffusion fronts and phase transitions are often linked to non-Fickian behaviour. However, by considering the time evolution of the complete concentration profiles in detail it is shown that the dissolution process can be explained using Fickian diffusion equations with a concentration-dependent diffusion coefficient. PMID:26018995

  12. A study on variation in dissolved silica concentration in groundwater of hard rock aquifers in Southeast coast of India

    NASA Astrophysics Data System (ADS)

    Pradeep, K.; Nepolian, M.; Anandhan, P.; Chandran; Kaviyarasan, R.; Prasanna, M. V.; Chidambaram, S.

    2016-03-01

    Ground water of hard rock aquifers due to its lesser permeability results in the increased residence time, which leads to the higher concentration of ions. Hence in order to understand the hydro-geochemistry of the groundwater of a hard rock aquifer in India, 23 groundwater samples were collected from different locations of the study area and subjected to analysis of major cations and anions. The results of silica showed different range of concentration and was plotted in different groups. In order to understand the reason for this variation, different techniques like Thermodynamics, Statistics and GIS were adopted and it was inferred that the concentration was mainly governed by lithology and land use pattern of the study area.

  13. In situ measurements of dissolved gases (CO2 and CH4) in a wide range of concentrations in a tropical reservoir using an equilibrator.

    PubMed

    Abril, Gwenaël; Richard, Sandrine; Guérin, Frédéric

    2006-02-01

    An equilibrator system connected to an infrared photo acoustic gas analyzer was used in order to measure directly in situ the concentrations of dissolved CO2 and CH4 in waters of a tropical reservoir (Petit Saut, French Guiana). The performance of the system was tested both on a vertical profile in the stratified water body of the reservoir and in the surface waters of the river downstream the dam. Results agreed with conventional GC analysis at +/-15% in a wide range of concentrations (CO2:50-400 micromol l-1 and CH4:0.5-350 micromol l-1 corresponding to gas partial pressures of respectively 1700-13,000 and 12-8800 microatm). The time needed for in situ measurements was equivalent to water sampling, time for GC analysis in the laboratory being suppressed. The continuous monitoring of gas concentrations for 24 h in the reservoir surface waters revealed rapid changes in concentrations highly significant in the daily emission budget. The system opens new perspectives for the monitoring of gas concentrations in highly dynamic systems like tropical reservoirs. PMID:16398998

  14. Electrolytic dissolver

    DOEpatents

    Wheelwright, E.J.; Fox, R.D.

    1975-08-26

    This patent related to an electrolytic dissolver 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 dissolved while permitting a free flow of electrolyte therebetween, means for passing a direct current between the electrodes and means for circulating electrolyte through the dissolver. (auth)

  15. Cloud water composition during HCCT-2010: Scavenging efficiencies, solute concentrations, and droplet size dependence of inorganic ions and dissolved organic carbon

    NASA Astrophysics Data System (ADS)

    van Pinxteren, D.; Fomba, K. W.; Mertes, S.; Müller, K.; Spindler, G.; Schneider, J.; Lee, T.; Collett, J.; Herrmann, H.

    2015-09-01

    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 dissolved organic carbon (DOC). Campaign volume-weighted mean concentrations 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 concentrations 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 concentrations and was found to have non-negligible impact on cloud water acidity. Relative standard deviations of major ions were 60-66 % for solute concentrations and 52-80 % for cloud water loadings (CWLs). Contrary to some earlier suggestions, the similar variability of solute concentrations and CWLs together with the results of back trajectory analysis and principal component analysis, suggests that concentrations in incoming air masses (i.e. air mass history), rather than cloud liquid water content (LWC) was the main factor controlling bulk solute concentrations 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 concentration) variations in a simple functional relation due to the complex processes involved. Bulk concentrations typically agreed within a factor of 2 with co-located measurements of residual particle concentrations sampled by a counterflow virtual impactor (CV) and analysed by an aerosol mass spectrometer (AMS), with the deviations being mainly

  16. Cloud water composition during HCCT-2010: Scavenging efficiencies, solute concentrations, and droplet size dependence of inorganic ions and dissolved organic carbon

    NASA Astrophysics Data System (ADS)

    van Pinxteren, Dominik; Wadinga Fomba, Khanneh; Mertes, Stephan; Müller, Konrad; Spindler, Gerald; Schneider, Johannes; Lee, Taehyoung; Collett, Jeffrey L.; Herrmann, Hartmut

    2016-03-01

    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 dissolved organic carbon (DOC). Campaign volume-weighted mean concentrations 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 concentrations 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 concentrations and was found to have non-negligible impact on cloud water acidity. Relative standard deviations of major ions were 60-66 % for solute concentrations and 52-80 % for cloud water loadings (CWLs). The similar variability of solute concentrations and CWLs together with the results of back-trajectory analysis and principal component analysis, suggests that concentrations in incoming air masses (i.e. air mass history), rather than cloud liquid water content (LWC), were the main factor controlling bulk solute concentrations 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 concentration) variations in a simple functional relation due to the complex processes involved. Bulk concentrations typically agreed within a factor of 2 with co-located measurements of residual particle concentrations sampled by a counterflow virtual impactor (CVI) and analysed by an aerosol mass spectrometer (AMS), with the deviations being mainly caused by systematic

  17. Environmental and toenail metals concentrations in copper mining and non mining communities in Zambia.

    PubMed

    Ndilila, Wesu; Callan, Anna Carita; McGregor, Laura A; Kalin, Robert M; Hinwood, Andrea L

    2014-01-01

    Copper mining contributes to increased concentrations of metals in the environment, thereby increasing the risk of metals exposure to populations living in and around mining areas. This study investigated environmental and toenail metals concentrations of non-occupational human exposure to metals in 39 copper-mining town residents and 47 non-mining town residents in Zambia. Elevated environmental concentrations were found in samples collected from the mining town residents. Toenail concentrations of cobalt (GM 1.39 mg/kg), copper (GM 132 mg/kg), lead (21.41 mg/kg) selenium (GM 0.38 mg/kg) and zinc (GM 113 mg/kg) were significantly higher in the mining area and these metals have previously been associated with copper mining. Residence in the mining area, drinking water, dust and soil metals concentrations were the most important contributors to toenail metals concentrations. Further work is required to establish the specific pathways of exposure and the health risks of elevated metals concentrations in the copper mining area. PMID:23623595

  18. Statistical Analysis Of Heavy Metals Concentration In Watermelon Plants Irrigated By Wastewater

    NASA Astrophysics Data System (ADS)

    Khanjani, M. J.; Maghsoudi moud, A. A.; Saffari, V. R.; Hashamipor, S. M.; Soltanizadeh, M.

    2008-01-01

    Concentration of heavy metals in vegetables irrigated by urban wastewater is a cause of serious concern due to the potentials health problems of consuming contaminated produce. In this study it is tried to model the concentration of heavy metals (Cd, Cr, Cu, Fe,…) as a function of their concentration in watermelon roots and stems. Our study shows there is a good relationship between them for most of collected data. By measuring the concentration in root and stem of watermelon plant samples before harvesting, the concentration of heavy metal in watermelon's fruit can be estimated by presented mathematical models. This study shows the concentrations of heavy metals in fruits, roots and stems of watermelon plants are very high and in dangerous level when irrigated by municipal waste water.

  19. What drove Dissolved Organic Carbon (DOC) concentration variability in the River Thames (UK) between 1884 and 2014?

    NASA Astrophysics Data System (ADS)

    Noacco, Valentina; Wagener, Thorsten; Howden, Nicholas; Duffy, Christopher

    2016-04-01

    Climate and atmospheric circulation patterns influence the variability of basin hydrochemistry, therefore understanding their influence is essential to put short-term water quality trends into the right context and to predict future hydrochemistry responses in the face of climate change. We investigate the drivers of DOC concentration variability in the Thames basin over 130 years. Our previous work has shown that increased urbanization since the 1880s in the Thames basin was the major driver for the increase in riverine DOC, but it does not explain DOC variability. Our current work investigates the links between hydro-climatic variability (temperature, precipitation and runoff) and teleconnections (ENSO and NAO), and the variability in DOC concentration. Moreover we compare the impact of hydro-climatic variability on riverine DOC, to the impact of land-use change and population increase. We use singular spectrum analysis to identify and then compare the dominant oscillatory components of hydro-climatic and hydro-biogeochemical variables. We use phase-plane trajectories of the noise-free, intra-annual to inter-annual reconstructed components to elucidate the biogeochemical and hydro-climatic dynamics of the system. This allows us to elucidate the links between the variability of hydro-climatic variables and DOC. Moreover they enable the identification of points in time where the dynamics of the system have changed, e.g. due to anthropogenic influences. Further, lag-correlations between teleconnections, DOC and flow are explored, to consider the hydrological memory of the catchment due to the permeable geology present. We show that the high seasonal to inter-annual variability in DOC concentration is linked to the variability of precipitation and runoff, rather than temperature. The dominant inter-annual modes of variability in DOC are connected to the ENSO oscillatory components. During strong El Niño and La Niña years there is statistically significant positive

  20. Dissolved pesticide concentrations in the Sacramento-San Joaquin Delta and Grizzly Bay, California, 2011-12

    USGS Publications Warehouse

    Orlando, James L.; McWayne, Megan; Sanders, Corey; Hladik, Michelle

    2013-01-01

    Surface-water samples were collected from sites within the Sacramento-San Joaquin Delta and Grizzly Bay, California, during the spring in 2011 and 2012, and they were analyzed by the U.S. Geological Survey for a suite of 99 current-use pesticides and pesticide degradates. Samples were collected and analyzed as part of a collaborative project studying the occurrence and characteristics of phytoplankton in the San Francisco Estuary. Samples were analyzed by two separate laboratory methods employing gas chromatography/mass spectrometry or liquid chromatography with tandem mass spectrometry. Method detection limits ranged from 0.9 to 10.5 nanograms per liter (ng/L). Eighteen pesticides were detected in samples collected during 2011, and the most frequently detected compounds were the herbicides clomazone, diuron, hexazinone and metolachlor, and the diuron degradates 3,4-dichloroaniline and N-(3,4-dichlorophenyl)-N’-methylurea (DCPMU). Concentrations for all compounds were less than 75 ng/L, except for the rice herbicide clomazone and the fungicide tetraconazole, which had maximum concentrations of 535 and 511 ng/L, respectively. In samples collected in 2012, a total of 16 pesticides were detected. The most frequently detected compounds were the fungicides azoxystrobin and boscalid and the herbicides diuron, hexazinone, metolachlor, and simazine. Maximum concentrations for all compounds detected in 2012 were less than 75 ng/L, except for the fungicide azoxystrobin and the herbicides hexazinone and simazine, which were detected at up to 188, 134, and 140 ng/L, respectively.

  1. Changes in the Dissolved Organic Carbon Concentrations of Stream and Soil Water in Response to a Watershed-Scale Calcium Addition and Recovery from Acidification

    NASA Astrophysics Data System (ADS)

    Fuss, C. B.; Driscoll, C. T.; Ard, G. R.

    2014-12-01

    Positive trends in surface water dissolved organic carbon (DOC) concentrations have been observed in recent decades across many, but not all, surface water monitoring sites in eastern North America and northern Europe. The drivers of these trends are not necessarily clear, although declining acidic deposition is often cited as a likely cause for increased DOC mobilization. Here we used long-term records (16-31 years) of monthly streamwater and soil solution chemistry data from two headwater catchments at the Hubbard Brook Experimental Forest (NH, USA) to evaluate DOC trends in response to the recovery from acidification. We compared the concentrations and trends of DOC in Hubbard Brook's Watershed 6 (W6) and Watershed 1 (W1). W6 is the biogeochemical reference watershed and W1 underwent a treatment with calcium silicate in 1999 to mitigate the effects of long-term acid deposition. Streamwater DOC in W6 initially decreased through the 1980s and 1990s, but has leveled over the past 10-15 years, coincident with a period of modest pH increase. In contrast, W1 streamwater DOC concentrations have significantly increased since the calcium treatment which has led to more marked increases in pH. Greater mobilization of DOC in soil solution in W1 appears to be driving the higher streamwater DOC concentrations. We are analyzing these trends spatially within the watersheds and in conjunction with major solute chemistry to further explain the observed changes in DOC.

  2. Calibration of UV/Vis spectrophotometers: A review and comparison of different methods to estimate TSS and total and dissolved COD concentrations in sewers, WWTPs and rivers.

    PubMed

    Lepot, Mathieu; Torres, Andres; Hofer, Thomas; Caradot, Nicolas; Gruber, Günter; Aubin, Jean-Baptiste; Bertrand-Krajewski, Jean-Luc

    2016-09-15

    UV/Vis spectrophotometers have been used for one decade to monitor water quality in various locations: sewers, rivers, wastewater treatment plants (WWTPs), tap water networks, etc. Resulting equivalent concentrations of interest can be estimated by three ways: i) by manufacturer global calibration; ii) by local calibration based on the provided global calibration and grab sampling; iii) by advanced calibration looking for relations between UV/Vis spectra and corresponding concentrations from grab sampling. However, no study has compared the applied methods so far. This collaborative work presents a comparison between five different methods. A Linear Regression (LR), Support Vector Machine (SVM), EVOlutionary algorithm method (EVO) and Partial Least Squares (PLS) have been applied on various data sets (sewers, rivers, WWTPs under dry, wet and all weather conditions) and for three water quality parameters: TSS, COD total and dissolved. Two criteria (r(2) and Root Mean Square Error RMSE) have been calculated - on calibration and verification data subsets - to evaluate accuracy and robustness of the applied methods. Values of criteria have then been statistically analysed for all and separated data sets. Non-consistent outcomes come through this study. According to the Kruskal-Wallis test and RMSEs, PLS and SVM seem to be the best methods. According to uncertainties in laboratory analysis and ranking of methods, LR and EVO appear more robust and sustainable for concentration estimations. Conclusions are mostly independent of water matrices, weather conditions or concentrations investigated. PMID:27295626

  3. Metal concentrations of wild edible mushrooms from Turkey.

    PubMed

    Sarikurkcu, Cengiz; Tepe, Bektas; Solak, Mehmet Halil; Cetinkaya, Serap

    2012-01-01

    In the present study, the contents of Zn, Fe, Cu, Mn, Co, Ni, Pb, Cd, Cr, Al, Ca, Mg, and K in Agaricus campestris, Agrocybe cylindracea, Collybia dryophila, Helvella leucopus, Russula delica, Tricholoma auratum, Amanita ovoidea, Melanoleuca excissa, Rhizopogon roseolus, Russula chloroides, Volvoriella gloiocephala, Lyophyllum decastes, Morcella angusticeps, Morchella esculenta and Morcella eximia collected from Isparta, Mugla, and Osmaniye provinces (Turkey) were determined by inductively coupled plasma optical emission spectrometry (ICP-OES) after microwave digestion. The intake of heavy metals (Pb, Cd) and other metals (Fe, Cu, Zn) by consumption of 30 g dry weight of mushrooms daily poses no risk at all except in A. cylindracea and H. leucopus (for Cd) for the consumer. PMID:22794131

  4. Atmospherically deposited trace metals from bulk mineral concentrate port operations.

    PubMed

    Taylor, Mark Patrick

    2015-05-15

    Although metal exposures in the environment have declined over the last two decades, certain activities and locations still present a risk of harm to human health. This study examines environmental dust metal and metalloid hazards (arsenic, cadmium, lead and nickel) associated with bulk mineral transport, loading and unloading port operations in public locations and children's playgrounds in the inner city of Townsville, northern Queensland. The mean increase in lead on post-play hand wipes (965 μg/m(2)/day) across all sites was more than 10-times the mean pre-play loadings (95 μg/m(2)/day). Maximum loading values after a 10-minute play period were 3012 μg/m(2), more than seven times the goal of 400 μg/m(2) used by the Government of Western Australia (2011). Maximum daily nickel post-play hand loadings (404 μg/m(2)) were more than 26 times above the German Federal Immission Control Act 2002 annual benchmark of 15 μg/m(2)/day. Repeat sampling over the 5-day study period showed that hands and surfaces were re-contaminated daily from the deposition of metal-rich atmospheric dusts. Lead isotopic composition analysis of dust wipes ((208)Pb/(207)Pb and (206)Pb/(207)Pb) showed that surface dust lead was similar to Mount Isa type ores, which are exported through the Port of Townsville. While dust metal contaminant loadings are lower than other mining and smelting towns in Australia, they exceeded national and international benchmarks for environmental quality. The lessons from this study are clear - even where operations are considered acceptable by managing authorities, targeted assessment and monitoring can be used to evaluate whether current management practices are truly best practice. Reassessment can identify opportunities for improvement and maximum environmental and human health protection. PMID:25706750

  5. 46 CFR 148.285 - Metal sulfide concentrates.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... concentrate unless— (1) The atmosphere in the cargo hold has been tested and contains sufficient oxygen to support life and, where the shipper indicates that toxic gas(es) may be generated, the atmosphere in...

  6. Tracing metal sources in core sediments of the artificial lake An-Dong, Korea: Concentration and metal association.

    PubMed

    Choi, Mansik; Park, Jongkyu; Cho, Dongjin; Jang, Dongjun; Kim, Miseon; Choi, Jongwoo

    2015-09-15

    The concentration and source of trace metals in the artificial lake An-Dong, which has widespread abandoned mines and a Zn smelter upstream of the drainage basin, were investigated. Soils (18ea), stream waters (15ea) and sediments (15ea) in the main channel and five tributaries downstream of the Zn smelter towards the lake (~ 50 km downstream) were collected. And two core sediments were also taken from the middle of the lake. All samples were analyzed for trace metals in bulk and in a 1N HCl-leached fraction. Although the soil and stream sediments consisted mostly of sand-sized grains, concentrations of metals (Cu, Zn, Cd and Pb) were very high in all samples, including soils, stream waters and sediments at sites near the Zn smelter. However the metal concentrations decreased rapidly downstream, suggesting that the area of impact of the smelter lies within 5 km. Highly enriched metal concentrations were also found in dated core sediments from the lake; while the highest concentrations of Co, Ni, As, Cu, Zn, Cd and Pb were detected in the bottom of the sediment core (dated 1980) they decreased towards 2000, and only Cu, Zn and Cd concentrations increased again in present-day samples. Since the temporal variation in metal concentrations appeared consistent with historical variation in ore mining and Zn smelter production rates, a model combining the production rates of each was developed, which estimated 3%, 12% and 7% contributions from Zn smelter compared to ore mining production rate to levels of Cu, Cd and Zn, respectively, suggesting the different pathways by different sources. In addition, analysis of Cd/Zn and Cu/Zn ratios showed that contamination from ore mining decreased from 1980 to 2000, and smelting processes were most likely responsible for metal enrichment (Cu, Cd and Zn) from 2000 to the present. PMID:25981937

  7. Anatomically-related variations in trace-metal concentrations in hair

    SciTech Connect

    DeAntonio, S.M.; Katz, S.A.; Scheiner, D.M.; Wood, J.D.

    1982-12-01

    Scalp-hair analysis is used as an indicator of trace-metal concentrations in the human body. The major shortcoming of this approach is the inability to differentiate between endogenous and exogenous trace metals. Our analyses show no correlation between the concentrations of calcium, magnesium, copper, iron, or zinc in scalp hair and pubic hair in 67 donor-matched hair samples. We interpret this as a strong indication that exogenous trace metals make a significant contribution to the results for trace metals in human hair.

  8. The effect of wind turbine-induced microclimates and plant functional types on peatland greenhouse gas emissions and pore water dissolved organic carbon concentrations

    NASA Astrophysics Data System (ADS)

    Armstrong, A.; Waldron, S.; Ostle, N.; Whitaker, J.

    2012-04-01

    Wind turbines can affect the local climate by removing energy from the wind and increasing air turbulence with a recent study showing a cooling effect of 1.5C during the day (Baidya & Roy, 2010). Wind farms are commonly located on peatlands where both greenhouse gas carbon dioxide (CO2) and methane (CH4) fluxes and dissolved organic carbon concentrations ([DOC]) are significantly influenced by temperature and water table depth. In this paper we present data from Black Law Wind Farm, Scotland, where we examined the effect of wind turbines on (1) Microclimate - peatland surface and subsurface temperatures, soil moisture and water table depth and (2) Carbon cycling - greenhouse gas fluxes and pore water dissolved organic carbon concentrations. Within our experimental framework we examined the impact of the three main peatland plant functional types (shrubs, mosses and sedges) and their interactions with wind microclimate changes on ecosystem CO2 and CH4 fluxes and [DOC]. The sampling plots are divided into four sites along a hypothesized wind turbine-induced microclimatic gradient. At each site twelve sampling plots were established, four in areas dominated by mosses, four in areas dominated by sedges and four in areas dominated by shrubs. The results show that there are significant relationships between plot location on the hypothesized microclimatic gradient, plant functional type and their interactions and CO2 and CH4 fluxes and [DOC]. Consequently, the long-term effects of wind farms on peatland microclimates may need to be taken into account when considering their life cycle carbon budget.

  9. Photosynthetic fractionation of 13C and concentrations of dissolved CO2 in the central equatorial Pacific during the last 255,000 years

    NASA Technical Reports Server (NTRS)

    Jasper, J. P.; Hayes, J. M.; Mix, A. C.; Prahl, F. G.

    1994-01-01

    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 dissolved 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 concentrations of dissolved 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 concentrations of dissolved 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

  10. Determination of Uranium Metal Concentration in Irradiated Fuel Storage Basin Sludge Using Selective Dissolution

    SciTech Connect

    Delegard, Calvin H.; Sinkov, Sergey I.; Chenault, Jeffrey W.; Schmidt, Andrew J.; Welsh, Terri L.; Pool, Karl N.

    2014-03-01

    Uranium metal corroding in water-saturated sludges now held in the US Department of Energy Hanford Site K West irradiated fuel storage basin can create hazardous hydrogen atmospheres during handling, immobilization, or subsequent transport and storage. Knowledge of uranium metal concentration in sludge thus is essential to safe sludge management and process design, requiring an expeditious routine analytical method to detect uranium metal concentrations as low as 0.03 wt% in sludge even in the presence of 30 wt% or higher total uranium concentrations.

  11. Quartz concentration trends in metal and nonmetal mining.

    PubMed

    Watts, Winthrop F; Huynh, Tran B; Ramachandran, Gurumurthy

    2012-01-01

    From 1974 through 2010, the Mine Safety and Health Administration (MSHA) collected nearly 147,000 respirable dust samples with a mass of at least 0.1 mg and a minimum of 1% quartz. These samples represent about 50% of all respirable dust compliance samples collected by MSHA. Analysis of these data shows that pockets of high concentrations and overexposure continue to exist. At underground mines, from 2005 to 2010, occupations with >20% of the samples exceeding the permissible exposure limit (PEL) and geometric mean quartz concentrations exceeding the ACGIH threshold limit value of 25 μg/m(3) included mucking, crusher operator, general laborer/utility, and front-end loader operator. During the same period, stone and rock saw operators and bagger and packers working at surface mines and mills also had >20% of the samples exceeding the PEL and geometric mean quartz concentrations >25 μg/m(3). Regardless of mine type or location, slow but steady improvement in exposure levels is seen in jobs involving crushing operations, which are widespread in the mining industry. Crusher operators are more likely to work in an enclosed area where it is easier to apply dust controls and air conditioning. A downward trend is also observed for vehicle equipment operators who drive load-haul-dumps, front-end loaders, trucks, and similar equipment. Crusher operators and vehicle equipment operators represent occupational categories that are widely sampled by MSHA inspectors. A small but statistically significant reduction in the overall mean respirable quartz dust and quartz concentrations from 1993 to 2010 was observed in most commodity groups. Variability from year to year and between commodities is high. Reduction in respirable quartz dust concentration does not necessarily correspond to a reduction in quartz concentration within the same commodity group. These trends are consistent with those reported in previous studies. PMID:23092305

  12. High concentrations of heavy metals in neighborhoods near ore smelters in northern Mexico.

    PubMed Central

    Benin, A L; Sargent, J D; Dalton, M; Roda, S

    1999-01-01

    In developing countries, rapid industrialization without environmental controls has resulted in heavy metal contamination of communities. We hypothesized that residential neighborhoods located near ore industries in three northern Mexican cities would be heavily polluted with multiple contaminants (arsenic, cadmium, and lead) and that these sites would be point sources for the heavy metals. To evaluate these hypotheses, we obtained samples of roadside surface dust from residential neighborhoods within 2 m of metal smelters [Torreón (n = 19)] and Chihuahua (n = 19)] and a metal refinery [Monterrey (n = 23)]. Heavy metal concentrations in dust were mapped with respect to distance from the industrial sites. Correlation between dust metal concentration and distance was estimated with least-squares regression using log-transformed data. Median dust arsenic, cadmium, and lead concentrations were 32, 10, and 277 microg/g, respectively, in Chihuahua; 42, 2, and 467 microg/g, respectively, in Monterrey, and 113, 112, and 2,448 microg/g, respectively, in Torreón. Dust concentrations of all heavy metals were significantly higher around the active smelter in Torreón, where more than 90% of samples exceeded Superfund cleanup goals. At all sites, dust concentrations were inversely related to distance from the industrial source, implicating these industries as the likely source of the contamination. We concluded that residential neighborhoods around metal smelting and refining sites in these three cities are contaminated by heavy metals at concentrations likely to pose a health threat to people living nearby. Evaluations of human exposure near these sites should be conducted. Because multiple heavy metal pollutants may exist near smelter sites, researchers should avoid attributing toxicity to one heavy metal unless others have been measured and shown not to coexist. Images Figure 1 Figure 2-3 Figure 4-5 Figure 6-7 Figure 8 PMID:10090706

  13. Equilibrium metal concentration at zero net sorption (EMC{sub 0}): A new concept

    SciTech Connect

    Yuan, G.; Lavkulich, L.M.

    1995-12-31

    Heavy metals in soils and waters are of environmental concerns. Since total concentration of a metal in soil is not directly related to its bioavailability, soil tests rely on measurement of extractable or labile fractions of metals. However, reagents used in the measurements are significantly different from natural waters entering soils in terms of ionic strength, acidity, and heavy metal concentration, making the direct interpretation of test results difficult if correlation between chemical test data and plant response in the field is not available. It is suggested that EMC{sub 0} be used as an indicator of heavy metal status in soils. EMC{sub 0} can be determined as follows: solutions with various metal concentrations (C{sub 0}) in 0.005 M CaCl{sub 2} matrix are added to soil samples at a fixed soil/solution ratio. The suspensions are shaken 24 hrs to achieve equilibrium, and centrifuged. Metal concentrations in supernatants are analyzed and plotted against C{sub 0}. A regression line based on plotted data an da 1:1 line are drawn. The X-axis value corresponding t the intersection of the liens is EMC{sub 0}. At the intersection, metal concentration at equilibrium equals that in the initial solution; indicating net sorption of the metal is zero. A EMC{sub 0} value of 0.27 mg/kg Zn was determined in a soil sample from the Fraser Valley in British Columbia. The soil received heavy applications of poultry manure.This value is much greater than water soluble Zn (0.06 mg/kg) of the sample. The significance of EMC{sub 0} is when concentrations of a metal in natural waters are less than EMC{sub 0}, soil will release the metal to soil solution. EMC{sub 0} may be useful in comparing relative degrees of contamination in contaminated soils.

  14. Geochemical behaviour of dissolved trace elements in a monsoon-dominated tropical river basin, Southwestern India.

    PubMed

    Gurumurthy, G P; Balakrishna, K; Tripti, M; Audry, Stéphane; Riotte, Jean; Braun, J J; Udaya Shankar, H N

    2014-04-01

    The study presents a 3-year time series data on dissolved 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 dissolved trace elements show seasonality in the river water metal concentrations forming two distinct groups of metals. First group is composed of heavy metals and minor elements that show higher concentrations during dry season and lesser concentrations during the monsoon season. Second group is composed of metals belonging to lanthanides and actinides with higher concentration in the monsoon and lower concentrations during the dry season. Although the metal concentration of both the groups appears to be controlled by the discharge, there are important biogeochemical processes affecting their concentration. 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 dissolved phase, whereas there is positive anomaly in the particulate and bed sediments. The Ce anomaly correlates with the variations in the dissolved oxygen indicating the redistribution of Ce between particulate and dissolved phase under acidic to neutral pH and lower concentrations of dissolved organic carbon. Unlike other

  15. PATTERNS AND CONTROLS OF DISSOLVED ORGANIC MATTER EXPORT BY MAJOR RIVERS: A NEW SEASONAL, SPATIALLY EXPLICIT, GLOBAL MODEL

    EPA Science Inventory

    River-derived dissolved organic matter (DOM) influences metabolism, light attenuation, and bioavailability of metals and nutrients in coastal ecosystems. Recent work suggests that DOM concentrations in surface waters vary seasonally because different organic matter pools are mobi...

  16. Silicic magma accumulation beneath Mount Mazama, Oregon, 71 ka to 24 ka constrained by SHRIMP measurements of dissolved volatile concentrations in melt inclusions

    NASA Astrophysics Data System (ADS)

    Wright, H. M.; Bacon, C. R.; Vazquez, J. A.; Sisson, T. W.

    2010-12-01

    Dissolved volatile contents of melt inclusions trapped in pyroxene and plagioclase crystals from 7 silicic eruptions preceding the climactic ~7.7 ka Mazama eruption were measured by SIMS with the Stanford-USGS SHRIMP-RG. Melt inclusions in crystals were intersected, polished, and crystals were mounted in indium in Al mounts. A 1.2-3.0 nA (depending on the session), O2- primary beam was accelerated and focused to a 15-25 μm spot on the sample surface, which generated positive secondary ions of analyzed Li, Be, B, C, OH, F, Mg, Si, SiH, S, Cl, Ca, AlO, KO, Rb, and Sr. Measurements were made at high mass resolution (6000-7000). Trace element and volatile concentrations were calculated using a best-fit regression to count rate ratios (normalized to 30Si) vs. variable known concentrations in experimental and natural rhyolite glass standards. Pumiceous samples were chosen from dacitic to rhyodacitic eruptive deposits, consisting of the 71ka dacite of Pumice Castle, 70ka dacite below Llao Rock, 50ka dacite of the Watchman, 35ka dacite of Munson Valley, 35ka Williams Crater tephra, 27ka Redcloud Cliff rhyodacite, and 24ka andesite S of Bear Bluff. Melt inclusions are abundant in spongy, mineral-inclusion-rich interiors of pyroxene crystals in early (71-35ka) eruptive deposits and are less abundant throughout pyroxenes from later eruptions (35-24ka) and in plagioclase crystals. Over the entire time interval, most trace element and volatile concentrations remain approximately constant between melt inclusion populations. However, there are some variations in water and carbon dioxide concentration. A large proportion of inclusions in the smaller eruptive deposits (0.003-0.4 km3) of the dacite of the Watchman, dacite of Munson Valley, and Williams Crater tephra have low water contents, ~1 wt% H2O, corresponding to a saturation pressure of 25MPa, or ~1km depth (at 870°, approximate average temperature for these deposits, e.g., Druitt and Bacon, Contrib Mineral Petrol 1989

  17. Metal concentrations in aggregate interiors, exteriors, whole aggregates, and bulk of Costa Rican soils

    SciTech Connect

    Wilcke, W.; Kretzschmar, S.; Bundt, M.; Zech, W.

    1999-10-01

    In many temperate soils the preferential weathering and leaching of aggregate surfaces and the nonaggregated material between aggregates depletes geogenic metals. It also shifts metals from strongly to more weakly bound metal forms. Deposited metals are sorbed preferentially on aggregate surfaces and between aggregates. The authors examined whether preferential desilication under tropical climate causes an enrichment in the aggregate exteriors in oxidic forms of metals. They also studied where deposited metals are bound in these soils. Aggregates (2--20 mm) were selected manually from the A horizons of eight Oxisols, six Andisols, two Mollisols, and two Inceptisols in Costa Rica. All samples were fractionated into interior and exterior portions and treated with a seven-step sequence to extract Al, Cd, Cu, Fe, Mn, Pb, and Zn. Total concentrations of all metals except Zn were higher in the aggregate exteriors than in the interiors. The average Cd and Pb concentrations in easily extractable fractions were significantly higher in the aggregate exteriors. There were no significant differences in metal partitioning between interiors and exteriors except for Pb, which had higher proportions in extractable forms with NH{sub 2}OH {center{underscore}dot} HCl {gt} NH{sub 4} - acetate, pH 6.0 {gt} EDTA in the exteriors. There were few significant differences in metal concentrations and partitioning between bulk soil and whole aggregates. The results may be explained by (i) preferential desilication of the aggregate exteriors and (ii) preferential sorption of deposited heavy metals mainly in easily extractable forms.

  18. Concentrations of phytochelatins and glutathione found in natural assemblages of seaweeds depend on species and metal concentrations of the habitat.

    PubMed

    Pawlik-Skowrońska, Barbara; Pirszel, Jacek; Brown, Murray T

    2007-07-20

    The occurrence of the metal-complexing thiol peptides, phytochelatins (PC) in natural populations of brown, red and green seaweeds (marine macroalgae) was studied. Concentrations of PCs and their precursor glutathione (GSH) were measured in seaweeds collected from locations in south-west England with different levels of contamination by trace metals, to evaluate their role under natural environmental conditions. The non-protein thiols were identified and quantified in seaweed extracts by HPLC and the molecular structures of PCs were confirmed by LC-ESIMS. The capacity for production of PCs of representative seaweeds under Cd and Zn exposure was also assessed, experimentally. The concentrations of metals/metalloids (As, Cu, Cd, Pb and Zn) accumulated by the seaweeds were determined by ICP-MS. For the first time, PCs are reported in native Phaeophyceae (Fucus spp.), Rhodophyceae (Solieria chordalis) and Chlorophyceae (Rhizoclonium tortuosum) but not in thalli of Ulva spp. and Codium fragile (Chlorophyceae). The concentrations of PCs in brown and red seaweeds correlated with the contamination history of sampling sites and total metal burden of thalli. The highest concentrations of metals (5.6-7.1micromolg(-1) DW), PCs (200-240nmolSHg(-1)DW) and GSH (1,550-3,960nmolSHg(-1)DW), and the longest PC chain lengths (PC(2-4)) were found in Fucus spp. collected from the most contaminated site. A combination of PC-production and maintenance of high concentrations of GSH allows Fucus spp. and R. tortuosum (2,000nmolGSHg(-1)DW) to thrive in highly contaminated environments whereas in Ulva spp. high concentrations of GSH (1,000-1,500nmolSHg(-1)DW) together with thick cells walls and a high polysaccharide content appear to be responsible for metal-resistance. The lack of production of PCs in these green macroalgae suggests lower intracellular metal accumulation rather than an inability for synthesizing PCs. The higher concentrations of Cu (approximately 3.4micromolg(-1)DW) found in

  19. Interspecific variation of metal concentrations in three bivalve mollusks from Galicia.

    PubMed

    Saavedra, Y; González, A; Fernández, P; Blanco, J

    2004-10-01

    There has been growing concern about the inflow of metals to the coastal areas because they can be toxic to aquatic and human life. Some studies have demonstrated the existence of species-specific differences in the metal concentrations of mollusks. We compared metal concentrations between Mytilus galloprovincialis, used as a water quality indicator, and two other bivalve species collected for human consumption (Venerupis pullastra and Cerastoderma edule) in different locations on the Galician coast (northwest Spain). M. galloprovincialis was found to be the best zinc and lead accumulator, whereas silver and arsenic were preferentially accumulated by V. pullastra and chromium and nickel by C. edule. Bivalve concentrations of mercury, cadmium, chromium, arsenic, silver, and zinc appeared to be linearly related to environmental concentrations, but this was not the case with copper, nickel, and lead in some species, which indicated that there is a nonlinear accumulation of these metals or an influence of the environmental conditions on species accumulation. The relationship between metal concentration in mussels and in the two other species varied with the metal and the species. In some cases the correlation was high, making it possible to use mussels as bioindicators for the other species. In other cases the correlation was moderate or low, therefore rendering mussels of little or no use in predicting the metal concentrations in the two other species. PMID:15386128

  20. Changes in dissolved organic material determine exposure of stream benthic communities to UV-B radiation and heavy metals: Implications for climate change

    USGS Publications Warehouse

    Clements, W.H.; Brooks, M.L.; Kashian, D.R.; Zuellig, R.E.

    2008-01-01

    Changes in regional climate in the Rocky Mountains over the next 100 years are expected to have significant effects on biogeochemical cycles and hydrological processes. In particular, decreased discharge and lower stream depth during summer when ultraviolet radiation (UVR) is the highest combined with greater photo-oxidation of dissolved organic materials (DOM) will significantly increase exposure of benthic communities to UVR. Communities in many Rocky Mountain streams are simultaneously exposed to elevated metals from abandoned mines, the toxicity and bioavailability of which are also determined by DOM. We integrated field surveys of 19 streams (21 sites) along a gradient of metal contamination with microcosm and field experiments conducted in Colorado, USA, and New Zealand to investigate the influence of DOM on bioavailability of heavy metals and exposure of benthic communities to UVR. Spatial and seasonal variation in DOM were closely related to stream discharge and significantly influenced heavy metal uptake in benthic organisms. Qualitative and quantitative changes in DOM resulting from exposure to sunlight increased UV-B (290-320nm) penetration and toxicity of heavy metals. Results of microcosm experiments showed that benthic communities from a metal-polluted stream were tolerant of metals, but were more sensitive to UV-B than communities from a reference stream. We speculate that the greater sensitivity of these communities to UV-B resulted from costs associated with metal tolerance. Exclusion of UVR from 12 separate Colorado streams and from outdoor stream microcosms in New Zealand increased the abundance of benthic organisms (mayflies, stoneflies, and caddisflies) by 18% and 54%, respectively. Our findings demonstrate the importance of considering changes in regional climate and UV-B exposure when assessing the effects of local anthropogenic stressors. ?? Journal compilation ?? 2008 Blackwell Publishing.

  1. Sediment Metal Concentration Survey Along the Mine-Affected Molonglo River, NSW, Australia.

    PubMed

    Wadige, Chamani P M Marasinghe; Taylor, Anne M; Krikowa, Frank; Maher, William A

    2016-04-01

    Metal concentrations were measured in sediments of the mine-affected Molonglo River to determine current metal concentrations and distribution along the river. Compared with an uncontaminated site at 6.5 km upstream of the Captains Flat mine, sediments collected from the river at ≤12.5 km distance below the mine had a significantly higher percentage of finely divided silt and clay with higher concentrations of cadmium (Cd), copper (Cu), lead (Pb), and zinc (Zn). The measured metal concentrations in the mine affected sites of the river were in the following order: Zn = 697-6818 > Pb = 23-1796 > Cu = 10-628 > Cd = 0.13-8.7 µg/g dry mass. The highest recorded metal concentrations were Cd at 48, Cu at 45, Pb at 240, and Zn at 81 times higher than the background concentrations of these metals in the river sediments. A clear sediment metal-contamination gradient from the mine site to 63 km downstream was established for Cd, Cu, Pb, and Zn in the river sediments. Compared with sediment metal concentrations before a major flood in 2010, only Zn concentrations increased. For all of the mine-affected sites studied, Cd and Zn concentrations exceeded the (ANZECC/ARMCANZ, Australian and New Zealand guidelines for fresh and marine water quality. Australian and New Zealand Environment and Conservation Council/Agriculture and Resource Management Council of Australia and New Zealand, 2000) interim sediment-quality guidelines low values for Cd (1.5 µg/g dry mass) and the high value for Zn (410 µg/g dry mass). Existing metal loads in the riverbed sediments may still be adversely affecting the river infauna. PMID:26795293

  2. Heavy metal concentrations in soil and earthworms in a floodplain grassland.

    PubMed

    van Vliet, P C J; van der Zee, S E A T M; Ma, W C

    2005-12-01

    We determined accumulated heavy metal concentrations (Cd, Pb, Cu, Zn) of earthworms in moderately contaminated floodplain soils. Both soil and mature earthworms were sampled before and after flooding and earthworm species were identified to understand species specific differences in bioconcentration. Accumulated metal concentrations in floodplain earthworms differed before and after flooding. Differences in uptake and elimination mechanisms, in food choice and living habitat of the different earthworm species and changes in speciation of the heavy metals are possible causes for this observation. Regression equations taken from literature, that relate metal accumulation by earthworms in floodplains as a function of metal concentration in soil, performed well when all species specific data were combined in an average accumulation, but did not address differences in accumulation between earthworm species. PMID:15951081

  3. Metal concentrations in cerebrospinal fluid and blood plasma from patients with amyotrophic lateral sclerosis.

    PubMed

    Roos, Per M; Vesterberg, Olof; Syversen, Tore; Flaten, Trond Peder; Nordberg, Monica

    2013-02-01

    Amyotrophic lateral sclerosis (ALS) is a progressive and fatal degenerative disorder of motor neurons. The cause of this degeneration is unknown, and different causal hypotheses include genetic, viral, traumatic and environmental mechanisms. In this study, we have analyzed metal concentrations in cerebrospinal fluid (CSF) and blood plasma in a well-defined cohort (n = 17) of ALS patients diagnosed with quantitative electromyography. Metal analyses were performed with high-resolution inductively coupled plasma mass spectrometry. Statistically significant higher concentrations of manganese, aluminium, cadmium, cobalt, copper, zinc, lead, vanadium and uranium were found in ALS CSF compared to control CSF. We also report higher concentrations of these metals in ALS CSF than in ALS blood plasma, which indicate mechanisms of accumulation, e.g. inward directed transport. A pattern of multiple toxic metals is seen in ALS CSF. The results support the hypothesis that metals with neurotoxic effects are involved in the pathogenesis of ALS. PMID:23225075

  4. Carbon nanofiber multiplexed array and Wireless Instantaneous Neurotransmitter Concentration Sensor for simultaneous detection of dissolved oxygen and dopamine

    PubMed Central

    Marsh, Michael P.; Koehne, Jessica E.; Andrews, Russell J.; Meyyappan, M.; Bennet, Kevin E.; Lee, Kendall H.

    2014-01-01

    Purpose While the mechanism of Deep Brain Stimulation (DBS) remains poorly understood, previous studies have shown that it evokes release of neurochemicals and induces activation of functional magnetic resonance imaging (fMRI) blood oxygen level-dependent signal in distinct areas of the brain. Therefore, the main purpose of this paper is to demonstrate the capabilities of the Wireless Instantaneous Neurotransmitter Concentration Sensor system (WINCS) in conjunction with a carbon nanofiber (CNF) multiplexed array electrode as a powerful tool for elucidating the mechanism of DBS through the simultaneous detection of multiple bioactive-molecules. Methods Patterned CNF nanoelectrode arrays were prepared on a 4-inch silicon wafer where each device consists of 3 × 3 electrode pads, 200 μm square, that contain CNFs spaced at 1μm intervals. The multiplexed carbon nanofiber CNF electrodes were integrated with WINCS to detect mixtures of dopamine (DA) and oxygen (O2) using fast scan cyclic voltammetry (FSCV) in vitro. Results First, simultaneous detection of O2 at two spatially different locations, 200 um apart, was demonstrated. Second, simultaneous detection of both O2 and DA at two spatially different locations, using two different decoupled waveforms was demonstrated. Third, controlled studies demonstrated that the waveform must be interleaved to avoid electrode crosstalk artifacts in the acquired data. Conclusions Multiplexed CNF nanoelectrode arrays for electrochemical detection of neurotransmitters show promise for the detection of multiple analytes with the application of time independent decoupled waveforms. Electrochemistry on CNF electrodes may be helpful in elucidating the mechanism of DBS, and may also provide the precision and sensitivity required for future applications in feedback modulated DBS neural control systems. PMID:24688800

  5. Distribution of the concentration of heavy metals associated with the sediment particles accumulated on road surfaces.

    PubMed

    Zafra, C A; Temprano, J; Tejero, I

    2011-07-01

    The heavy metal pollution caused by road run-off water constitutes a problem in urban areas. The metallic load associated with road sediment must be determined in order to study its impact in drainage systems and receiving waters, and to perfect the design of prevention systems. This paper presents data regarding the sediment collected on road surfaces in the city of Torrelavega (northern Spain) during a period of 65 days (132 samples). Two sample types were collected: vacuum-dried samples and those swept up following vacuuming. The sediment loading (g m(-2)), particle size distribution (63-2800 microm) and heavy metal concentrations were determined. The data showed that the concentration of heavy metals tends to increase with the reduction in the particle diameter (exponential tendency). The concentrations ofPb, Zn, Cu, Cr, Ni, Cd, Fe, Mn and Co in the size fraction <63 microm were 350, 630, 124, 57, 56, 38, 3231, 374 and 51 mg kg(-1), respectively (average traffic density: 3800 vehicles day(-1)). By increasing the residence time of the sediment, the concentration increases, whereas the ratio of the concentration between the different size fractions decreases. The concentration across the road diminishes when the distance between the roadway and the sampling siteincreases; when the distance increases, the ratio between size fractions for heavy metal concentrations increases. Finally, the main sources of heavy metals are the particles detached by braking (brake pads) and tyre wear (rubber), and are associated with particle sizes <125 microm. PMID:21882553

  6. Fe and Cu isotope fractionation between chalcopyrite and dissolved metal species during hydrothermal recrystallization: An experimental study at 350°C and 500 bars

    NASA Astrophysics Data System (ADS)

    Syverson, D. D.; Luhmann, A. J.; Tan, C.; Borrok, D. M.; Ding, K.; Seyfried, W. E., Jr.

    2015-12-01

    The equilibrium Fe and Cu isotope fractionation factor between chalcopyrite and dissolved metal species was determined under hydrothermal conditions at 350°C and 500 bars. The experiments took advantage of gold-cell reaction technology, allowing time-series sampling of solution during the hydrothermal recrystallization of chalcopyrite over 3000 hours. One of the recrystallization experiments utilized an anomalous 57Fe spike in solution to quantify the degree and rate of isotopic exchange towards equilibrium between mineral and fluid reservoirs. The time-series 57Fe spike data suggests that chalcopyrite exchanges rapidly with dissolved Fe and Cu in solution and the isotopic fractionation between each metal-bearing reservoir throughout reaction progress, upon dissolution and recrystallization, represents close to equilibrium conditions. The isotope data indicate that the equilibrium fractionation between chalcopyrite and dissolved Fe and Cu at 350°C, Δ56FeCpy-Fe(aq), is 0.129±0.171‰ and Δ65CuCpy-Fe(aq), is -0.201±0.341‰ (2σ), and are in good agreement with recent theoretical equilibrium predictions. Comparison of the experimental data from this study with conjugate chalcopyrite and dissolved Fe and Cu pairs from a variety of hydrothermal systems along the mid-ocean ridge system indicates that chalcopyrite precipitates and recrystallizes at isotopic equilibrium with the fluid during cooling upon ascent to the seafloor. The rapid exchange between the mineral and fluid metal-reservoirs suggests that chalcopyrite effectively records the isotopic composition of the coexisting hydrothermal fluid during the evolution of hydrothermal systems. In addition, the pyrite-chalcopyrite equilibrium Fe isotope fractionation, Δ56FePyr-Cpy, at 350°C is quantified by combination of pyrite-Fe2+(aq) equilibrium fractionation data from Syverson et al., [2013] with chalcopyrite-Fe2+(aq) from this study, resulting in a fractionation of 0.861±0.337‰ (2σ). The empirical

  7. Application of patent bio-rack wetland system using Phragmites sp. for domestic wastewater treatment in the presence of high total dissolved solids (TDS) and heavy metal salts.

    PubMed

    Valipour, Alireza; Raman, V Kalyan; Ghole, V S

    2011-07-01

    The quality of water recourses is degrading due to improper wastewater management. The aim of this study is to examine the potential of bio-rack system for treatment of domestic wastewater in the presence of high total dissolved solids (TDS) and heavy metal salts. The bio-rack is a modified wetland system incorporated with the advantages of phytoremediation and attached growth microbial process. The bio-rack is void of the soil strata based root zone system and in lieu a support matrix is provided to enrich the micro flora. The studies indicate that, Phragmites sp. can tolerate TDS up to 9000 mg/L in the bio-rack. The heavy metal removal is a function of phytoaccumulation or phytoextraction, which can lead to morphological deformity if heavy metals exceed the saturation limit of 786 and 5760 mg/kg Cd, 854 and 9280 mg/kg Cu, 639 and 4720 mg/kg Ni, 1187 and 7516 mg/kg Zn, in shoots and roots respectively. The reduction in TDS is marginal (14%) at the highest tolerable limit whereas the heavy metal reduction is 68%, 69%, 67%, 71% for Cd, Cu, Ni and Zn respectively at the outlet of the treatment system. The sewage treatment performance of the bio-rack system for all other parameters is estimated as 75 % Chemical Oxygen Demand (COD), 86 % Biological Oxygen Demand (BOD5), 27% Total Dissolved Solids (TDS), 73% Total Suspended Solids (TSS), 9% chlorides, 70% ammonia nitrogen (NH3-N), 32% phosphate (PO4-P), 92% most probable number (MPN) and 93% total viable count (TVC) reduction. PMID:23029929

  8. Heavy metal variation and characterization change of dissolved organic matter (DOM) obtained from composting or vermicomposting pig manure amended with maize straw.

    PubMed

    Zhu, Weiqin; Yao, Wu; Du, Wenhui

    2016-06-01

    A mixture of pig manure and maize straw was vermicomposted with Eisenia fetida or naturally composted for 60 days; basic parameters, heavy metal variation, dissolved organic matter (DOM) content, and its characterization were determined, aiming to explore different dynamics of DOM characterization and heavy metal variation during composting or vermicomposting. The results showed that vermicomposting led to higher pH, TC, and available P but lower EC, TN, available N, and available K in the substrate residues compared with natural composting; the total or available Cu/Zn content in the substrate residues similarly increased after composting or vermicomposting, but Cu was easily enriched in earthworm bodies and its intestinal vermicompost while vermicomposting enhanced the formation of dissolved Zn in DOM; moreover, much more fulvic and humic acid-like materials and much greater aromaticity were exhibited in DOM obtained from vermicomposting residues compared with DOM from composting residues, which may contribute to the variations of Cu/Zn enrichment in earthworms and its migration to the vermicomposting residues or its DOM. PMID:26971511

  9. PREDICTING ESTUARINE SEDIMENT METAL CONCENTRATIONS AND INFERRED ECOLOGICAL CONDITIONS: AN INFORMATION THEORETIC APPROACH

    EPA Science Inventory

    Empirically derived values associating sediment metal concentrations with degraded ecological conditions provide important information to assess estuarine condition. However, resources limit the number, magnitude, and frequency of monitoring programs to gather these data. As su...

  10. Superovulation in ewes by a single injection of pFSH dissolved in polyvinylpyrrolidone (PVP): effects of PVP molecular weight, concentration and schedule of treatment.

    PubMed

    D'Alessandro, A G; Martemucci, G; Colonna, M A; Borghese, A; Terzano, M G; Bellitti, A

    2001-03-30

    Three experiments were carried out to evaluate induction in ewes of superovulation and embryo production by a single injection of a porcine pituitary extract (pFSH) dissolved in polyvinylpyrrolidone (PVP), investigating the effects of PVP molecular weight and its concentration (Experiment I), time and method of treatment (Experiments II and III). All ewes were synchronized for estrus by vaginal sponges impregnated with fluorogestone acetate (FGA; 30 mg, 9 days) plus PGF(2alpha) (Cloprostenol, 50 microg, 48h before sponge removal - s.r.), and superovulated by 250 IU pFSH. In Experiment I, 60 Gentile di Puglia ewes were subdivided into five experimental groups (n = 12): Group A, the control, received six decreasing intramuscular (i.m.) doses of pFSH, 12 h apart, beginning 48h before s.r.; Groups B and C were given 48 h before s.r. a single i.m. injection of pFSH dissolved in PVP with MW = 10,000, respectively, at concentrations of 15 and 30% w/v; Groups D and E received the same treatments as for B and C using PVP with MW = 40,000. None of the pFSH-PVP treatments were effective in inducing superovulation. In Experiment II, 22 Leccese ewes were subdivided into two groups (n = 11): Group A, control received i.m. four decreasing doses of pFSH, beginning 24 h before s.r., 12h apart; Group B was given a single i.m. injection of pFSH dissolved in PVP (MW = 40,000 at 30% w/v), 24 h before s.r. The pFSH-PVP treatment provided an ovulation rate similar to the control and tended to enhance embryo yield (4.4 versus 2.4, P>0.05). In Experiment III, 60 Leccese ewes were subdivided into six treatment groups (n = 10). Groups A and D served as controls and received i.m. 12 h apart, six doses (from 48 h before s.r.) and four doses (from 24h before s.r.) of pFSH, respectively. Groups B and C were treated by a single injection of pFSH in PVP (MW = 10,000; 30% w/v) 48 h before s.r., respectively by i.m. or subcutaneous (s.c.) administration. Groups E and F received the same treatments

  11. Interspecific and geographical variations of trace metal concentrations in cephalopods from Tunisian waters.

    PubMed

    Rjeibi, Moncef; Metian, Marc; Hajji, Tarek; Guyot, Thierry; Ben Chaouacha-Chékir, Rafika; Bustamante, Paco

    2014-06-01

    The concentrations of six metals (Ag, Cd, Cu, Hg, Pb, and Zn) were investigated and compared in three tissues (arms, digestive gland, and mantle) of three cephalopod species from the Tunisian waters: the common octopus (Octopus vulgaris), the common cuttlefish (Sepia officinalis), and the European squid (Loligo vulgaris). Whatever the species or the sites, the digestive gland displayed the highest concentrations of Ag, Cd, Cu, Pb, and Zn, highlighting its major role in their bioaccumulation and detoxification. This is also true for Hg but only for the digestive gland of O. vulgaris. Muscle from the arms and the mantle contained thus relatively low trace metal concentrations except for Hg in L. vulgaris and S. officinalis. Geographic comparison of metal concentrations in Tunisian cephalopods from three locations indicates that higher concentrations of Ag, Pb, and Hg were observed in cephalopods from northern and eastern coasts, whereas the highest Cd levels were detected in the southeastern, reflecting different conditions of exposure. Comparing the trace element concentrations between species, Ag, Cd, Cu, Hg, and Zn concentrations were the highest in the digestive gland of octopuses. This may be related to the differences in ecological features and swimming behavior among different cephalopod species. Effects of length and sex on metal levels were also considered, indicating a limited influence of sex on metal concentration. PMID:24562415

  12. Heavy metal concentrations (Cd, Cu and Pb) in five aquatic plant species in Tasik Chini, Malaysia

    NASA Astrophysics Data System (ADS)

    Ebrahimpour, M.; Mushrifah, I.

    2008-04-01

    The purpose of this study was to determine the levels of heavy metals namely cadmium (Cd), copper (Cu) and lead (Pb) in the five aquatic plants. For this purpose, the concentration of heavy metals were measured in water and in the five aquatic plant species, Lepironia articulata, Pandanus helicopus, Scirpus grossus, Cabomba furcata and Nelumbo nucifera, in 15 sites from Tasik Chini. The concentrations were different among the plant species as well as among the parts of plants. The highest concentration of heavy metals among the aquatic plants and plant parts was found in the roots of S. grossus. The concentrations of Cd in the leaves and stems of submerged aquatic plant, C . furcata, were higher than concentration of Cd in the leaves and stems of emergent aquatic plant and floating leaf plant. The concentration of Cu in the stem of C. furcata was greater than that in the leaf, while the concentration of Cd was more in the leaf than in the stem. The heavy metal contents of the aquatic plants were in descending order of Pb > Cu > Cd. The metal concentration quotient of leaves/roots and stems/roots (ML/MR and MS/MR) were calculated. The highest internal translocation was found in P. helicopus, while the lowest internal translocation was found in S. grossus.

  13. Heavy metals in plants in constructed and natural wetlands: concentration, accumulation and seasonality.

    PubMed

    Vymazal, J; Březinová, T

    2015-01-01

    The accumulation of heavy metals in plants is a function of uptake capacity and intracellular binding sites. The concentrations of heavy metals in plants growing in constructed wetlands vary considerably between species and systems but in general, the concentrations are within the range commonly found in natural stands. The highest concentrations are mostly found in roots, followed by rhizomes, leaves and stems. Unfortunately, concentration values are commonly used to evaluate the 'accumulation' of heavy metals, but this approach is not correct. In order to evaluate heavy metal accumulation, the biomass of particular plant parts must be taken into consideration. In addition, there are two other factors, which need to be taken into consideration when accumulation is evaluated, namely seasonality and distribution within the plant shoot. It has been found that the seasonal distribution of heavy metals in the biomass varies between heavy metals and mostly does not follow the pattern known for nutrients. In addition, the concentration and accumulation of heavy metals vary considerably within the shoot and this fact should be taken into consideration when analyses are carried out. PMID:25633951

  14. Factors affecting metal concentrations in the upper sediment layer of intertidal reedbeds along the river Scheldt.

    PubMed

    Du Laing, Gijs; Vandecasteele, Bart; De Grauwe, Pieter; Moors, Wouter; Lesage, Els; Meers, Erik; Tack, Filip M G; Verloo, Marc G

    2007-05-01

    Factors that play a role in determining metal accumulation in sediments of 26 intertidal marshes which are mainly vegetated by reed plants (Phragmites australis) were assessed along the Scheldt estuary (Belgium and The Netherlands). In the upper 20 cm sediment layer, several physico-chemical properties (clay, silt and sand content, organic matter, carbonate and chloride content, pH and conductivity) and aqua regia extractable metals (Cd, Cr, Cu, Ni, Pb, Zn) were determined. The sediments were significantly contaminated with trace metals. The Cd concentrations often exceeded the Flemish soil remediation thresholds for nature areas, whereas Cr, Cu and Zn levels indicated moderate contamination. Pb concentrations occasionally were high, whereas Ni concentrations leaned towards background values. Organic matter was the single most important predictor variable for total metal contents in regression models, except for Cr. Additional significant predictor variables were clay or chloride content, depending on the metal. Observed metal concentrations at sites within a range of a few km from specific point-sources of metals (e.g. shipyards, industrial areas with metallurgic activities, affluents, major motorways) were somewhat higher than predicted by the models, whereas they were lower than predicted at sites which are regularly subjected to flooding by water of high salinity. The ratio between observed and predicted concentrations seems to be a valuable tool for the identification of areas which are specifically impacted by point sources. PMID:17492090

  15. Computed solid phases limiting the concentration of dissolved constituents in basalt aquifers of the Columbia Plateau in eastern Washington. Geochemical modeling and nuclide/rock/groundwater interaction studies

    SciTech Connect

    Deutsch, W.J.; Jenne, E.A.; Krupka, K.M.

    1982-08-01

    A speciation-solubility geochemical model, WATEQ2, was used to analyze geographically-diverse, ground-water samples from the aquifers of the Columbia Plateau basalts in eastern Washington. The ground-water samples compute to be at equilibrium with calcite, which provides both a solubility control for dissolved calcium and a pH buffer. Amorphic ferric hydroxide, Fe(OH)/sub 3/(A), is at saturation or modestly oversaturated in the few water samples with measured redox potentials. Most of the ground-water samples compute to be at equilibrium with amorphic silica (glass) and wairakite, a zeolite, and are saturated to oversaturated with respect to allophane, an amorphic aluminosilicate. The water samples are saturated to undersaturated with halloysite, a clay, and are variably oversaturated with regard to other secondary clay minerals. Equilibrium between the ground water and amorphic silica presumably results from the dissolution of the glassy matrix of the basalt. The oversaturation of the clay minerals other than halloysite indicates that their rate of formation lags the dissolution rate of the basaltic glass. The modeling results indicate that metastable amorphic solids limit the concentration of dissolved silicon and suggest the same possibility for aluminum and iron, and that the processes of dissolution of basaltic glass and formation of metastable secondary minerals are continuing even though the basalts are of Miocene age. The computed solubility relations are found to agree with the known assemblages of alteration minerals in the basalt fractures and vesicles. Because the chemical reactivity of the bedrock will influence the transport of solutes in ground water, the observed solubility equilibria are important factors with regard to chemical-retention processes associated with the possible migration of nuclear waste stored in the earth's crust.

  16. Small mammal-heavy metal concentrations from mined and control sites

    USGS Publications Warehouse

    Smith, G.J.; Rongstad, O.J.

    1982-01-01

    Total body concentrations of zinc, copper, cadmium, lead, nickel, mercury and arsenic were determined for Peromyscus maniculatus and Microtus pennsylvanicus from an active zinc-copper mine near Timmins, Ontario, Canada, and a proposed zinc-copper mine near Crandon, Wisconsin, USA. Metal concentrations were evaluated with respect to area, species, sex and age groups. Metal concentrations in Peromyscus from the proposed mine site were not different from those collected in a third area where no mine or deposit exists. This is probably due to the 30 m of glacial material over the proposed mine site deposit. A statistical interaction between area, species, sex and age was observed for zinc and copper concentrations in small mammals we examined. Peromyscus from the mine site had consistently higher metal concentrations than Peromyscus from the control site. Greater total body cadmium and lead concentrations in adult?compared with juvenile?Peromyscus collected at the mine site suggests age-dependent accumulation of these toxic metals. Microtus did not exhibit this age-related response, and responded to other environmental metals more erratically and to a lesser degree. Differences in the response of these two species to environmental metal exposure may be due to differences in food habits. Nickel, mercury and arsenic concentrations in small mammals from the mine site were not different from controls. Heavy metal concentrations are also presented for Sorex cinereus, Blarina brevicauda and Zapus hudsonicus without respect to age and sex cohorts. Peromyscus may be a potentially important species for the monitoring of heavy metal pollution.

  17. Predicting the toxicity of metal-contaminated field sediments using interstitial concentration of metals and acid-volatile sulfide normalizations

    SciTech Connect

    Hansen, D.J.; Berry, W.J.; Mahony, J.D.

    1996-12-01

    The authors investigated the utility of interstitial water concentrations of metals and simultaneously extracted metal/acid-volatile sulfide (SEM/AVS) ratios to explain the biological availability of sediment-associated divalent metals to benthic organisms exposed in the laboratory to sediments from five saltwater and four freshwater locations in the US, Canada, and China. The amphipod Ampelisca abdita or the polychaete Neanthes arenaceodentata were exposed to 70 sediments from the five saltwater locations, and the amphipod Hyalella azteca or the oligochaete Lumbriculus variegatus were exposed to 55 sediments from four freshwater locations in 10-d lethality tests. Almost complete absence of toxicity in spiked sediments and field sediments where metals were the only known source of contamination and where interstitial water toxic units (IWTUs) were < 0.5 indicates that toxicity associated with sediments having SEM/AVS ratios < 1.0 from two saltwater locations in industrial harbors was not metals-related as these sediments contained <0.5 IWTU. Metals-associated toxicity was absent in 100% of sediments from the remaining three saltwater field locations, where metals were the only known source of contamination and SEM/AVS ratios were {le} 1.0. Two-thirds of 45 sediments from seven saltwater and freshwater field locations having both IWTUs > 0.5 (55%) were used alone. The difference between the molar concentrations of SEM and AVS (SEM-AVS) can provide important insight into the extent of additional available binding capacity, the magnitude by which AVS binding has been exceeded, and, when organism response is considered, the potential magnitude of importance of other metal binding phases. SEM-AVS should be used instead of SEM/AVS ratios as a measure of metals availability. In published experiments with both metal-spiked and field sediments, SEM-AVS and IWTUs accurately identified absence of sediment toxicity and with less accuracy identified the presence of toxicity.

  18. Using environmental isotopes and dissolved methane concentrations to constrain hydrochemical processes and inter-aquifer mixing in the Galilee and Eromanga Basins, Great Artesian Basin, Australia

    NASA Astrophysics Data System (ADS)

    Moya, Claudio E.; Raiber, Matthias; Taulis, Mauricio; Cox, Malcolm E.

    2016-08-01

    Groundwater recharge processes, water-rock interaction and the hydraulic connectivity between aquifers of the Galilee and Eromanga Basins in central Queensland, Australia, were investigated using stable (δ2H, δ18O, δ13C and 87Sr/86Sr) and radiogenic (36Cl) isotopes and dissolved methane concentrations, complemented by major ion chemistry. The central Eromanga and the upper sequence of the Galilee basins are both sub-basins of the Great Artesian Basin (GAB), and the coal seams of the Galilee Basin are currently explored for their potential as commercial coal seam gas deposits. In order to understand the potential influence of depressurisation of coal seams required to release the gas on adjacent aquifers, a detailed understanding of recharge processes and groundwater hydraulics of these basins prior to any development is required. Each of the different isotope systems were used in this study to provide different information on specific processes. For example, the assessment of δ13C and 87Sr/86Sr ratios suggested that carbonate dissolution is one of the major processes controlling the water chemistry within some aquifers. In addition, the combined assessment of δ2H, δ18O and major ion chemistry indicates that transpiration is the primary process controlling the solute concentration in the GAB recharge area, whereas evaporation appears to be less significant. Groundwaters in the Galilee Basin recharge area (outside the limits of the GAB) are different to any groundwater within the GAB units. This difference is attributed to the dissolution of potassium-bearing micas, which are absent in the GAB. Groundwater age estimates based on 36Cl/Cl ratios suggest that there is a steady increase along the flow paths, and this lack of anomalous age estimates from the recharge areas to the deeper parts of the basin indicates that there is no evidence for regional inter-aquifer mixing based in isotopes only. However, dissolved methane concentrations and groundwater chemistry

  19. Heavy metals' concentration in sediment, shrimp and two fish species from the northwest Persian Gulf.

    PubMed

    Monikh, Fazel Abdolahpur; Maryamabadi, Ammar; Savari, Ahmad; Ghanemi, Kamal

    2015-06-01

    The concentrations of heavy metals (cadmium (Cd), copper (Cu), nickel (Ni), lead (Pb) and zinc (Zn)) were measured in hepatopancreas and muscle of a commercial shrimp (Metapenaeus affinis), in the muscle, liver and gills of two fish species (Thryssa vitrirostris and Johnius belangerii) and in the sediment samples taken from the mouth of the Arvand river, Meleh estuary and Musa estuary in the northeast Persian Gulf. Concentration of heavy metals varied depending on different tissues, species and sampling sites. Liver of fish and hepatopancreas of shrimp exhibited higher metals' concentration than the other tissues. Generally, in the mouth of the Arvand river, the highest concentration of metals was found in benthic species; while in the mouth of Musa estuary, the highest level of the metals was found in pelagic fish species. Bioaccumulation factors were observed to follow the order: J. belangerii-liver-Cd > T. vitrirostris-liver-Pb > M. affinis-hepatopancreas-Zn >M. affinis-hepatopancreas-Cu >M. affinis- hepatopancreas-Ni. The analysed heavy metals were found in sediment samples at mean concentration in the sediment quality guideline proposed by National Oceanic and Atmospheric Administration (NOAA) and Regional Organization for the Protection of The Marine Environment (ROPME), except for Ni concentration in some cases. PMID:23406960

  20. Influence of Dissolved Organic Matter on the Solubility of Heavy Metals in Sewage-Sludge-Amended Soils

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Sewage sludge-amended soils generally contain elevated levels of organic matter and heavy metals compared to control soils. Since organic matter is known to complex with heavy metals, the solubility behavior of the organic matter in such soils may exert a significant influence on the solubility of t...

  1. Influence of aeration-homogenization system in stirred tank bioreactors, dissolved oxygen concentration and pH control mode on BHK-21 cell growth and metabolism.

    PubMed

    Núñez, Eutimio Gustavo Fernández; Leme, Jaci; de Almeida Parizotto, Letícia; Chagas, Wagner Antonio; de Rezende, Alexandre Gonçalves; da Costa, Bruno Labate Vale; Monteiro, Daniela Cristina Ventini; Boldorini, Vera Lucia Lopes; Jorge, Soraia Attie Calil; Astray, Renato Mancini; Pereira, Carlos Augusto; Caricati, Celso Pereira; Tonso, Aldo

    2014-08-01

    This work focused on determining the effect of dissolved oxygen concentration (DO) on growth and metabolism of BHK-21 cell line (host cell for recombinant proteins manufacturing and viral vaccines) cultured in two stirred tank bioreactors with different aeration-homogenization systems, as well as pH control mode. BHK-21 cell line adapted to single-cell suspension was cultured in Celligen without aeration cage (rotating gas-sparger) and Bioflo 110, at 10, 30 and 50 % air saturation (impeller for gas dispersion from sparger-ring). The pH was controlled at 7.2 as far as it was possible with gas mixtures. In other runs, at 30 and 50 % (DO) in Bioflo 110, the cells grew at pH controlled with CO2 and NaHCO3 solution. Glucose, lactate, glutamine, and ammonium were quantified by enzymatic methods. Cell concentration, size and specific oxygen consumption were also determined. When NaHCO3 solution was not used, the optimal DOs were 10 and 50 % air saturation for Celligen and Bioflo 110, respectively. In this condition maximum cell concentrations were higher than 4 × 10(6) cell/mL. An increase in maximum cell concentration of 36 % was observed in batch carried out at 30 % air saturation in a classical stirred tank bioreactor (Bioflo 110) with base solution addition. The optimal parameters defined in this work allow for bioprocess developing of viral vaccines, transient protein expression and viral vector for gene therapy based on BHK-21 cell line in two stirred tank bioreactors with different agitation-aeration systems. PMID:23846480

  2. Accuracy of different sensors for the estimation of pollutant concentrations (total suspended solids, total and dissolved chemical oxygen demand) in wastewater and stormwater.

    PubMed

    Lepot, Mathieu; Aubin, Jean-Baptiste; Bertrand-Krajewski, Jean-Luc

    2013-01-01

    Many field investigations have used continuous sensors (turbidimeters and/or ultraviolet (UV)-visible spectrophotometers) to estimate with a short time step pollutant concentrations 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 concentrations of total suspended solids (TSS), total and dissolved 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. PMID:23863442

  3. Impact of dissolved inorganic carbon concentrations and pH on growth of the chemolithoautotrophic epsilonproteobacterium Sulfurimonas gotlandica GD1T

    PubMed Central

    Mammitzsch, Kerstin; Jost, Günter; Jürgens, Klaus

    2014-01-01

    Epsilonproteobacteria have been found globally distributed in marine anoxic/sulfidic areas mediating relevant transformations within the sulfur and nitrogen cycles. In the Baltic Sea redox zones, chemoautotrophic epsilonproteobacteria mainly belong to the Sulfurimonas gotlandica GD17 cluster for which recently a representative strain, S. gotlandica GD1T, could be established as a model organism. In this study, the potential effects of changes in dissolved inorganic carbon (DIC) and pH on S. gotlandica GD1T were examined. Bacterial cell abundance within a broad range of DIC concentrations and pH values were monitored and substrate utilization was determined. The results showed that the DIC saturation concentration for achieving maximal cell numbers was already reached at 800 μmol L−1, which is well below in situ DIC levels. The pH optimum was between 6.6 and 8.0. Within a pH range of 6.6–7.1 there was no significant difference in substrate utilization; however, at lower pH values maximum cell abundance decreased sharply and cell-specific substrate consumption increased. PMID:24376054

  4. Dissolved pesticide concentrations detected in storm-water runoff at selected sites in the San Joaquin River basin, California, 2000-2001

    USGS Publications Warehouse

    Orlando, James L.; Kuivila, Kathryn M.; Whitehead, Andrew

    2003-01-01

    As part of a collaborative study involving the United States Geological Survey Toxics Substances Hydrology Project (Toxics Project) and the University of California, Davis, Bodega Marine Laboratory (BML), water samples were collected at three sites within the San Joaquin River Basin of California and analyzed for dissolved pesticides. Samples were collected during, and immediately after, the first significant rainfall (greater than 0.5 inch per day) following the local application of dormant spray, organophosphate insecticides during the winters of 2000 and 2001. All samples were collected in conjunction with fish-caging experiments conducted by BML researchers. Sites included two locations potentially affected by runoff of agricultural chemicals (San Joaquin River near Vernalis, California, and Orestimba Creek at River Road near Crows Landing, California, and one control site located upstream of pesticide input (Orestimba Creek at Orestimba Creek Road near Newman, California). During these experiments, fish were placed in cages and exposed to storm runoff for up to ten days. Following exposure, the fish were examined for acetylcholinesterase concentrations and overall genetic damage. Water samples were collected throughout the rising limb of the stream hydrograph at each site for later pesticide analysis. Concentrations of selected pesticides were measured in filtered water samples using solid-phase extraction (SPE) and gas chromatography-mass spectrometry (GC/MS) at the U.S. Geological Survey organic chemistry laboratory in Sacramento, California. Results of these analyses are presented.

  5. A passive sampler based on solid phase microextraction (SPME) for sediment-associated organic pollutants: Comparing freely-dissolved concentration with bioaccumulation.

    PubMed

    Maruya, Keith A; Lao, Wenjian; Tsukada, David; Diehl, Dario W

    2015-10-01

    The elevated occurrence of hydrophobic organic chemicals (HOCs) such as polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCBs) and legacy organchlorine pesticides (e.g. chlordane and DDT) in estuarine sediments continues to poses challenges for maintaining the health of aquatic ecosystems. Current efforts to develop and apply protective, science-based sediment quality regulations for impaired waterbodies are hampered by non-concordance between model predictions and measured bioaccumulation and toxicity. A passive sampler incorporating commercially available solid phase microextraction (SPME) fibers was employed in lab and field studies to measure the freely dissolved concentration of target HOCs (Cfree) and determine its suitability as a proxy for bioaccumulation. SPME deduced Cfree for organochlorines was highly correlated with tissue concentrations (Cb) of Macoma and Nereis spp. co-exposed in laboratory microcosms containing both spiked and naturally contaminated sediments. This positive association was also observed in situ for endemic bivalves, where SPME samplers were deployed for up to 1 month at an estuarine field site. The concordance between Cb and Cfree for PAH was more variable, in part due to likely biotransformation by model invertebrates. These results indicate that SPME passive samplers can serve as a proxy for bioaccumulation of sediment-associated organochlorines in both lab and field studies, reducing the uncertainty associated with model predictions that do not adequately account for differential bioavailability. PMID:26246043

  6. Particle concentration effect: adsorption of divalent metal ions on coffee grounds.

    PubMed

    Utomo, Handojo Djati; Hunter, Keith A

    2010-03-01

    The adsorption of divalent metal ions Cu2+, Pb2+, Zn2+, and Cd2+ on coffee grounds as a function of coffee grounds concentration was studied in which adsorption density decreased as the concentration of coffee grounds (C(s)) increased. Adsorption studies were conducted by equilibrating aqueous solutions of each metal ion at concentrations in the range 19-291 micromol L(-1) with coffee suspensions in the concentration range 0.971-8.738 g L(-1), with the initial pH adjusted to 5.0+/-0.1 using NaOH or HNO3. Metastable Equilibrium Adsorption theory did not adequately explain the adsorption phenomenon, except at low concentrations of coffee grounds and trace metal ions. Instead the results indicated that flocculation might reduce the surface availability thus reducing the adsorption density. The flocculation theory was confirmed after a further experiment adding dispersant sodium hexa-meta-phosphate (NaHMP) to the suspension. PMID:19660940

  7. Morphological abnormalities in chironomidae in relation to sediment metals concentrations in Empire Lake, Cherokee County, Kansas

    SciTech Connect

    Ferringington, L.C. Jr.

    1994-12-31

    Morphological abnormalities of headcapsule structures of chironomid larvae were quantified in relation to concentrations of heavy metals in sediments of Empire Lake. This reservoir is situated in a catchment downstream of a US EPA Superfund Site in the Tri-State Mining District of southeast Kansas, and receives discharges from several streams that flow through the abandoned mining areas. Sediments have elevated concentrations of Zinc, Lead, and Cadmium in varying concentrations. Chironomini had the highest incidence of morphological abnormalities, followed by Procladius. Although deformities of the mentum, premandibles, and antennae were found in several taxa, no clear trends were seen for increasing concentrations of any of the metals individually or collectively. From this study it appears as if the incidence of morphological abnormalities is not a linear function of metals concentrations in sediments of this reservoir.

  8. Heavy metal concentrations in roadside soils and correlation with urban traffic in Beijing, China.

    PubMed

    Chen, Xi; Xia, Xinghui; Zhao, Ye; Zhang, Ping

    2010-09-15

    A detailed investigation was conducted to study the heavy metal concentrations in roadside soils of Beijing. The concentrations of Cd, Cu, Pb and Zn showed a decreasing trend with increasing distance from the road while such trend was not identified in As, Cr and Ni. In addition, the concentrations of Cd, Cu, Pb and Zn significantly positively correlated with black carbon (BC) and TOC (p<0.01). The soil samples from West 2nd Ring Road with the highest traffic