Sample records for vapour ice seawater

  1. Estimates of ikaite export from sea ice to the underlying seawater in a sea ice-seawater mesocosm

    NASA Astrophysics Data System (ADS)

    Geilfus, Nicolas-Xavier; Galley, Ryan J.; Else, Brent G. T.; Campbell, Karley; Papakyriakou, Tim; Crabeck, Odile; Lemes, Marcos; Delille, Bruno; Rysgaard, Søren

    2016-09-01

    The precipitation of ikaite and its fate within sea ice is still poorly understood. We quantify temporal inorganic carbon dynamics in sea ice from initial formation to its melt in a sea ice-seawater mesocosm pool from 11 to 29 January 2013. Based on measurements of total alkalinity (TA) and total dissolved inorganic carbon (TCO2), the main processes affecting inorganic carbon dynamics within sea ice were ikaite precipitation and CO2 exchange with the atmosphere. In the underlying seawater, the dissolution of ikaite was the main process affecting inorganic carbon dynamics. Sea ice acted as an active layer, releasing CO2 to the atmosphere during the growth phase, taking up CO2 as it melted and exporting both ikaite and TCO2 into the underlying seawater during the whole experiment. Ikaite precipitation of up to 167 µmol kg-1 within sea ice was estimated, while its export and dissolution into the underlying seawater was responsible for a TA increase of 64-66 µmol kg-1 in the water column. The export of TCO2 from sea ice to the water column increased the underlying seawater TCO2 by 43.5 µmol kg-1, suggesting that almost all of the TCO2 that left the sea ice was exported to the underlying seawater. The export of ikaite from the ice to the underlying seawater was associated with brine rejection during sea ice growth, increased vertical connectivity in sea ice due to the upward percolation of seawater and meltwater flushing during sea ice melt. Based on the change in TA in the water column around the onset of sea ice melt, more than half of the total ikaite precipitated in the ice during sea ice growth was still contained in the ice when the sea ice began to melt. Ikaite crystal dissolution in the water column kept the seawater pCO2 undersaturated with respect to the atmosphere in spite of increased salinity, TA and TCO2 associated with sea ice growth. Results indicate that ikaite export from sea ice and its dissolution in the underlying seawater can potentially hamper

  2. Numerical implementation and oceanographic application of the thermodynamic potentials of water, vapour, ice, seawater and air - Part 2: The library routines

    NASA Astrophysics Data System (ADS)

    Wright, D. G.; Feistel, R.; Reissmann, J. H.; Miyagawa, K.; Jackett, D. R.; Wagner, W.; Overhoff, U.; Guder, C.; Feistel, A.; Marion, G. M.

    2010-03-01

    The SCOR/IAPSO1 Working Group 127 on Thermodynamics and Equation of State of Seawater has prepared recommendations for new methods and algorithms for numerical estimation of the thermophysical properties of seawater. As an outcome of this work, a new International Thermodynamic Equation of Seawater (TEOS-10) was endorsed by IOC/UNESCO2 in June 2009 as the official replacement and extension of the 1980 International Equation of State, EOS-80. As part of this new standard a source code package has been prepared that is now made freely available to users via the World Wide Web. This package includes two libraries referred to as the SIA (Sea-Ice-Air) library and the GSW (Gibbs SeaWater) library. Information on the GSW library may be found on the TEOS-10 web site (http://www.TEOS-10.org). This publication provides an introduction to the SIA library which contains routines to calculate various thermodynamic properties as discussed in the companion paper. The SIA library is very comprehensive, including routines to deal with fluid water, ice, seawater and humid air as well as equilibrium states involving various combinations of these, with equivalent code developed in different languages. The code is hierachically structured in modules that support (i) almost unlimited extension with respect to additional properties or relations, (ii) an extraction of self-contained sub-libraries, (iii) separate updating of the empirical thermodynamic potentials, and (iv) code verification on different platforms and between different languages. Error trapping is implemented to identify when one or more of the primary routines are accessed significantly beyond their established range of validity. The initial version of the SIA library is available in Visual Basic and FORTRAN as a supplement to this publication and updates will be maintained on the TEOS-10 web site. 1 SCOR/IAPSO: Scientific Committee on Oceanic Research

  3. Green icebergs formed by freezing of organic-rich seawater to the base of Antarctic ice shelves

    NASA Technical Reports Server (NTRS)

    Warren, Stephen G.; Roesler, Collin S.; Morgan, Vincent I.; Brandt, Richard E.; Goodwin, Ian D.; Allison, Ian

    1993-01-01

    Samples of Antarctic seawater, basal ice, and green ice from ice cliffs and green icebergs are analyzed in order to examine green icebergs formed by the freezing of organic-rich seawater to the base of Antarctic ice shelves. Spectral reflectance of a green iceberg measured near 67 deg S, 62 deg E confirms that the color is inherent in the ice, not an artifact of the illumination. A constituent that absorbs blue photons is identified by spectrophotometric analysis of core samples from this iceberg and from the Amery basal ice, and of seawater samples from Prydz Bay off the Amery Ice Shelf. Analysis of the samples by fluorescence spectroscopy indicates that the blue absorption, and hence the inherent green color, is due to the presence of marine-derived organic matter in the green iceberg, basal ice, and seawater. Thick accumulations of green ice, in icebergs, and at the base of ice shelves indicate that high concentrations of organic matter exist in seawater for centuries at the depth of basal freezing.

  4. Green icebergs formed by freezing of organic-rich seawater to the base of Antarctic ice shelves

    NASA Astrophysics Data System (ADS)

    Warren, Stephen G.; Roesler, Collin S.; Morgan, Vincent I.; Brandt, Richard E.; Goodwin, Ian D.; Allison, Ian

    1993-01-01

    Although most icebergs are blue, green icebergs are seen occasionally in the Antarctic ocean. Chemical and isotopic analysis of samples from green icebergs indicate that the ice consists of desalinated frozen seawater, as does the basal ice from the Amery Ice Shelf. Spectral reflectance of a green iceberg measured near 67°S, 62°E, confirms that the color is inherent to the ice, not an artifact of the illumination. Pure ice appears blue owing to its absorption of red photons. Addition of a constituent that absorbs blue photons can shift the peak reflectance from blue to green. Such a constituent was identified by spectrophotometric analysis of core samples from this iceberg and from the Amery basal ice, and of seawater samples from Prydz Bay off the Amery Ice Shelf. Analysis of the samples by fluorescence spectroscopy indicates that the blue absorption, and hence the inherent green color, is due to the presence of marine-derived organic matter in the green iceberg, basal ice, and seawater. Thick accumulations of green ice, in icebergs and at the base of ice shelves, indicate that high concentrations of organic matter exist in seawater for centuries at the depth of basal freezing.

  5. Numerical implementation and oceanographic application of the thermodynamic potentials of liquid water, water vapour, ice, seawater and humid air - Part 2: The library routines

    NASA Astrophysics Data System (ADS)

    Wright, D. G.; Feistel, R.; Reissmann, J. H.; Miyagawa, K.; Jackett, D. R.; Wagner, W.; Overhoff, U.; Guder, C.; Feistel, A.; Marion, G. M.

    2010-07-01

    The SCOR/IAPSO1 Working Group 127 on Thermodynamics and Equation of State of Seawater has prepared recommendations for new methods and algorithms for numerical estimation of the the thermophysical properties of seawater. As an outcome of this work, a new International Thermodynamic Equation of Seawater (TEOS-10) was endorsed by IOC/UNESCO2 in June 2009 as the official replacement and extension of the 1980 International Equation of State, EOS-80. As part of this new standard a source code package has been prepared that is now made freely available to users via the World Wide Web. This package includes two libraries referred to as the SIA (Sea-Ice-Air) library and the GSW (Gibbs SeaWater) library. Information on the GSW library may be found on the TEOS-10 web site (http://www.TEOS-10.org). This publication provides an introduction to the SIA library which contains routines to calculate various thermodynamic properties as discussed in the companion paper. The SIA library is very comprehensive, including routines to deal with fluid water, ice, seawater and humid air as well as equilibrium states involving various combinations of these, with equivalent code developed in different languages. The code is hierachically structured in modules that support (i) almost unlimited extension with respect to additional properties or relations, (ii) an extraction of self-contained sub-libraries, (iii) separate updating of the empirical thermodynamic potentials, and (iv) code verification on different platforms and between different languages. Error trapping is implemented to identify when one or more of the primary routines are accessed significantly beyond their established range of validity. The initial version of the SIA library is available in Visual Basic and FORTRAN as a supplement to this publication and updates will be maintained on the TEOS-10 web site. 1SCOR/IAPSO: Scientific Committee on Oceanic Research

  6. Competition for water vapour results in suppression of ice formation in mixed-phase clouds

    NASA Astrophysics Data System (ADS)

    Simpson, Emma L.; Connolly, Paul J.; McFiggans, Gordon

    2018-05-01

    The formation of ice in clouds can initiate precipitation and influence a cloud's reflectivity and lifetime, affecting climate to a highly uncertain degree. Nucleation of ice at elevated temperatures requires an ice nucleating particle (INP), which results in so-called heterogeneous freezing. Previously reported measurements for the ability of a particle to nucleate ice have been made in the absence of other aerosol which will act as cloud condensation nuclei (CCN) and are ubiquitous in the atmosphere. Here we show that CCN can outcompete INPs for available water vapour thus suppressing ice formation, which has the potential to significantly affect the Earth's radiation budget. The magnitude of this suppression is shown to be dependent on the mass of condensed water required for freezing. Here we show that ice formation in a state-of-the-art cloud parcel model is strongly dependent on the criteria for heterogeneous freezing selected from those previously hypothesised. We have developed an alternative criteria which agrees well with observations from cloud chamber experiments. This study demonstrates the dominant role that competition for water vapour can play in ice formation, highlighting both a need for clarity in the requirements for heterogeneous freezing and for measurements under atmospherically appropriate conditions.

  7. Seawater and Detrital Marine Pb Isotopes as Monitors of Antarctic Weathering Following Ice Sheet Development

    NASA Astrophysics Data System (ADS)

    Fenn, C.; Martin, E. E.; Basak, C.

    2011-12-01

    Comparisons of seawater and detrital Pb isotopes from sites proximal to Antarctica at the Eocene/Oligocene transition (EOT) are being used to understand variations in continental weathering associated with the development of the East Antarctic Ice Sheet (EAIS). Previous work has shown that seawater and detrital archives yield similar isotopic values during Eocene warmth, which is interpreted to record congruent chemical weathering of the continent. In contrast, distinct isotopic values for the two phases at the EOT represents increased incongruent mechanical weathering during growth of the ice sheet. For this study we expanded beyond the initial glaciation at the EOT to determine whether less dramatic changes in ice volume and climate also produce variations in weathering and intensity that are recorded by seawater and detrital Pb isotopes. We collected Nd and Pb isotope data from extractions of Fe-Mn oxide coatings of bulk decarbonated marine sediments, which preserve seawater isotopic values, and from complete dissolutions of the remaining silicate fraction for Ocean Drilling Program Site 748 on Kerguelen Plateau (1300 m modern water depth). The data spans an interval of deglaciation from ~23.5-27 Ma documented by δ18O that has been equated to a ~30% decrease in ice volume on Antarctica (Pekar and Christie-Blick, 2008, Palaeogeogr., Palaeoclim., Palaeoecol.). Initial results from Site 748 include the first ɛNd values for intermediate waters in the Oligocene Southern Ocean and reveal a value of ~-8 over the entire 3.5 my interval, which is consistent with values reported for deep Indian Ocean sites at this time and similar to deeper Southern Ocean sites. Corresponding detrital ɛNd values are less radiogenic and decrease from -9 to -13 during the study interval. Detrital 206Pb/204Pb values also decrease during the warming interval, while seawater 206Pb/204Pb values increase. The decrease in detrital values indicates the composition of source materials entering

  8. Seasonally-Active Water on Mars: Vapour, Ice, Adsorbate, and the Possibility of Liquid

    NASA Astrophysics Data System (ADS)

    Richardson, M. I.

    2002-12-01

    Seasonally-active water can be defined to include any water reservoir that communicates with other reservoirs on time scales of a year or shorter. It is the interaction of these water reservoirs, under the influence of varying solar radiation and in conjunction with surface and atmospheric temperatures, that determines the phase-stability field for water at the surface, and the distribution of water in various forms below, on, and above the surface. The atmosphere is the critical, dynamical link in this cycling system, and also (fortunately) one of the easiest to observe. Viking and Mars Global Surveyor observations paint a strongly asymmetric picture of the global seasonal water cycle, tied proximately to planetary eccentricity, and the existence of residual ice caps of different composition at the two poles. The northern summer experiences the largest water vapour columns, and is associated with sublimation from the northern residual water ice cap. The southern summer residual carbon dioxide ice cap is cold trap for water. Asymmetry in the water cycle is an unsolved problem. Possible solutions may involve the current timing of perihelion (the water cap resides at the pole experiencing the longer but cooler summer), the trapping of water ice in the northern hemisphere by tropical water ice clouds, and the bias in the annual-average, zonal-mean atmospheric circulation resulting from the zonal-mean difference in the elevation of the northern and southern hemispheres. Adsorbed and frozen water have proven harder to constrain. Recent Odyssey Gamma Ray Spectrometer results suggest substantial ground ice in the mid- and high-latitudes, but this water is likely below the seasonal skin depth for two reasons: the GRS results are best fit with such a model, and GCM models of the water cycle produce dramatically unrealistic atmospheric vapour distributions when such a very near surface, GRS-like distribution is initialized - ultimately removing the water to the northern and

  9. Ice-nucleating particles in Canadian Arctic sea-surface microlayer and bulk seawater

    NASA Astrophysics Data System (ADS)

    Irish, Victoria E.; Elizondo, Pablo; Chen, Jessie; Chou, Cédric; Charette, Joannie; Lizotte, Martine; Ladino, Luis A.; Wilson, Theodore W.; Gosselin, Michel; Murray, Benjamin J.; Polishchuk, Elena; Abbatt, Jonathan P. D.; Miller, Lisa A.; Bertram, Allan K.

    2017-09-01

    The sea-surface microlayer and bulk seawater can contain ice-nucleating particles (INPs) and these INPs can be emitted into the atmosphere. Our current understanding of the properties, concentrations, and spatial and temporal distributions of INPs in the microlayer and bulk seawater is limited. In this study we investigate the concentrations and properties of INPs in microlayer and bulk seawater samples collected in the Canadian Arctic during the summer of 2014. INPs were ubiquitous in the microlayer and bulk seawater with freezing temperatures in the immersion mode as high as -14 °C. A strong negative correlation (R = -0. 7, p = 0. 02) was observed between salinity and freezing temperatures (after correction for freezing depression by the salts). One possible explanation is that INPs were associated with melting sea ice. Heat and filtration treatments of the samples show that the INPs were likely heat-labile biological materials with sizes between 0.02 and 0.2 µm in diameter, consistent with previous measurements off the coast of North America and near Greenland in the Arctic. The concentrations of INPs in the microlayer and bulk seawater were consistent with previous measurements at several other locations off the coast of North America. However, our average microlayer concentration was lower than previous observations made near Greenland in the Arctic. This difference could not be explained by chlorophyll a concentrations derived from satellite measurements. In addition, previous studies found significant INP enrichment in the microlayer, relative to bulk seawater, which we did not observe in this study. While further studies are needed to understand these differences, we confirm that there is a source of INP in the microlayer and bulk seawater in the Canadian Arctic that may be important for atmospheric INP concentrations.

  10. Effects of seawater flow rate and evaporation temperature on performance of Sherbet type ice making machine

    NASA Astrophysics Data System (ADS)

    Son, C. H.; Yoon, J. I.; Choi, K. H.; Lee, H. K.; Lee, K. S.; Moon, C. G.; Seol, S. H.

    2018-01-01

    This study analyzes performance of the sherbet type ice making machine using seawater with respect to seawater volumetric flow rate, evaporation temperature, cooling water inlet and seawater inlet temperature as variables. Cooling water inlet and seawater inlet temperature are set considering average temperature of South Korea and the equator regions. Volumetric flow rate of seawater range is 0.75-1.75 LPM in this experiment. The results obtained from the experiment are as follows. As the seawater volumetric flow rate increases, or seawater inlet temperature increases, evaporation capacity tends to increase. At the point of seawater inlet temperature of 27°C and volumetric flow rate of 1.0LPM, evaporation capacity is over 2kW. On the other hand, results of COP change tendency are different from that of evaporation capacity. It appears to increase until volumetric flow rate of 1.0LPM, and decrease gradually from volumetric flow rate of 1.5LPM. This is due to the increase of compressor work to keep the evaporation pressure in accordance with the temperature of heat source. As the evaporation temperature decreases from -8 to -15°C, the evaporation capacity increases, but the COP decreases.

  11. No sodium in the vapour plumes of Enceladus.

    PubMed

    Schneider, Nicholas M; Burger, Matthew H; Schaller, Emily L; Brown, Michael E; Johnson, Robert E; Kargel, Jeffrey S; Dougherty, Michele K; Achilleos, Nicholas A

    2009-06-25

    The discovery of water vapour and ice particles erupting from Saturn's moon Enceladus fuelled speculation that an internal ocean was the source. Alternatively, the source might be ice warmed, melted or crushed by tectonic motions. Sodium chloride (that is, salt) is expected to be present in a long-lived ocean in contact with a rocky core. Here we report a ground-based spectroscopic search for atomic sodium near Enceladus that places an upper limit on the mixing ratio in the vapour plumes orders of magnitude below the expected ocean salinity. The low sodium content of escaping vapour, together with the small fraction of salt-bearing particles, argues against a situation in which a near-surface geyser is fuelled by a salty ocean through cracks in the crust. The lack of observable sodium in the vapour is consistent with a wide variety of alternative eruption sources, including a deep ocean, a freshwater reservoir, or ice. The existing data may be insufficient to distinguish between these hypotheses.

  12. Numerical simulation of flow and melting characteristics of seawater-ice crystals two-phase flow in inlet straight pipe of shell and tube heat exchanger of polar ship

    NASA Astrophysics Data System (ADS)

    Xu, Li; Huang, Chang-Xu; Huang, Zhen-Fei; Sun, Qiang; Li, Jie

    2018-05-01

    The ice crystal particles are easy to enter into the seawater cooling system of polar ship together with seawater when it sails in the Arctic. They are easy to accumulate in the pipeline, causing serious blockage of the cooling pipe. In this study, the flow and melting characteristics of ice particles-seawater two-phase flow in inlet straight pipe of shell-and-tube heat exchanger were numerically simulated by using Eulerian-Eulerian two-fluid model coupled with the interphase heat and mass transfer model. The influences of inlet ice packing factor, ice crystal particle diameter, and inlet velocity on the distribution and melting characteristics of ice crystals were investigated. The degree of asymmetry of the distribution of ice crystals in the cross section decreases gradually when the IPF changes from 5 to 15%. The volume fractions of ice crystals near the top of the outlet cross section are 19.59, 19.51, and 22.24% respectively for ice packing factor of 5, 10 and 15%. When the particle diameter is 0.5 mm, the ice crystals are gradually stratified during the flow process. With particle diameters of 1.0 and 2.0 mm, the region with the highest volume fraction of ice crystals is a small circle and the contours in the cloud map are compact. The greater the inlet flow velocity, the less stratified the ice crystals and the more obvious the turbulence on the outlet cross section. The average volume fraction of ice crystals along the flow direction is firstly rapidly reduced and then stabilized after 300 mm.

  13. The Effects of Freezing, Melting and Partial Ice Cover on Gas Transport in Laboratory Seawater Experiments

    NASA Astrophysics Data System (ADS)

    Loose, B.; McGillis, W.; Schlosser, P.; Perovich, D.; Takahashi, T.

    2008-12-01

    Sea ice physico-chemical processes affect gas dynamics, which may be relevant to polar ocean budgets of climatically-active gases. We used SF6 and O2 as inert gas tracers in a tank experiment to observe the transport of gases between water, ice and air during freezing/melting and partial ice cover. The results show that during ice growth, the rejection of O2 and SF6 was greater than the rejection of salt per unit of ambient concentration in seawater. Unconsolidated ice crystal growth produced an increase in dissolved O2 concentration, indicating that the water-air gradient may favor gas evasion during the early stages of sea-ice formation. Measurements of the gas transfer velocity (k), using SF6 and O2 during conditions of partial ice cover exceed the proportionality between the fraction of open water and k determined between 0% and 100% open water conditions. At 15% open water, k equals 35% of k during ice-free conditions, indicating the importance of under-ice turbulence for gas exchange. In our experiments most of this turbulence was produced by pumps installed for circulation of the water in the tank to avoid density stratification. Varying the turbulent kinetic energy (TKE) delivered to the water by these pumps produced a correspondent variation in k. Measurements of TKE using particle velocimetry suggest that turbulence in the ice-water boundary layer dominated the convection driven by heat loss through the open water, and the magnitude of net TKE production was similar to that measured beneath drifting ice in the field.

  14. Methane-oxidizing seawater microbial communities from an Arctic shelf

    NASA Astrophysics Data System (ADS)

    Uhlig, Christiane; Kirkpatrick, John B.; D'Hondt, Steven; Loose, Brice

    2018-06-01

    Marine microbial communities can consume dissolved methane before it can escape to the atmosphere and contribute to global warming. Seawater over the shallow Arctic shelf is characterized by excess methane compared to atmospheric equilibrium. This methane originates in sediment, permafrost, and hydrate. Particularly high concentrations are found beneath sea ice. We studied the structure and methane oxidation potential of the microbial communities from seawater collected close to Utqiagvik, Alaska, in April 2016. The in situ methane concentrations were 16.3 ± 7.2 nmol L-1, approximately 4.8 times oversaturated relative to atmospheric equilibrium. The group of methane-oxidizing bacteria (MOB) in the natural seawater and incubated seawater was > 97 % dominated by Methylococcales (γ-Proteobacteria). Incubations of seawater under a range of methane concentrations led to loss of diversity in the bacterial community. The abundance of MOB was low with maximal fractions of 2.5 % at 200 times elevated methane concentration, while sequence reads of non-MOB methylotrophs were 4 times more abundant than MOB in most incubations. The abundances of MOB as well as non-MOB methylotroph sequences correlated tightly with the rate constant (kox) for methane oxidation, indicating that non-MOB methylotrophs might be coupled to MOB and involved in community methane oxidation. In sea ice, where methane concentrations of 82 ± 35.8 nmol kg-1 were found, Methylobacterium (α-Proteobacteria) was the dominant MOB with a relative abundance of 80 %. Total MOB abundances were very low in sea ice, with maximal fractions found at the ice-snow interface (0.1 %), while non-MOB methylotrophs were present in abundances similar to natural seawater communities. The dissimilarities in MOB taxa, methane concentrations, and stable isotope ratios between the sea ice and water column point toward different methane dynamics in the two environments.

  15. Turbulent heat transfer as a control of platelet ice growth in supercooled under-ice ocean boundary layers

    NASA Astrophysics Data System (ADS)

    McPhee, Miles G.; Stevens, Craig L.; Smith, Inga J.; Robinson, Natalie J.

    2016-04-01

    Late winter measurements of turbulent quantities in tidally modulated flow under land-fast sea ice near the Erebus Glacier Tongue, McMurdo Sound, Antarctica, identified processes that influence growth at the interface of an ice surface in contact with supercooled seawater. The data show that turbulent heat exchange at the ocean-ice boundary is characterized by the product of friction velocity and (negative) water temperature departure from freezing, analogous to similar results for moderate melting rates in seawater above freezing. Platelet ice growth appears to increase the hydraulic roughness (drag) of fast ice compared with undeformed fast ice without platelets. Platelet growth in supercooled water under thick ice appears to be rate-limited by turbulent heat transfer and that this is a significant factor to be considered in mass transfer at the underside of ice shelves and sea ice in the vicinity of ice shelves.

  16. Theoretical model of the Bergeron-Findeisen mechanism of ice crystal growth in clouds

    NASA Astrophysics Data System (ADS)

    Castellano, N. E.; Avila, E. E.; Saunders, C. P. R.

    A numerical study of growth rate of ice particles in an array of water droplets (Bergeron-Findeisen mechanism) has used the method of electrostatic image charges to determine the vapour field in which a particle grows. Analysis of growth rate in various conditions of relevance to clouds has shown that it is proportional to liquid water content and to ice particle size, while it is inversely proportional to cloud droplet size. The results show that growth rate is enhanced by several percent relative to the usual treatment in which vapour is assumed to diffuse from infinity towards a growing ice particle. The study was performed for ice particles between 25 and 150 μm radii, water droplet sizes between 6 and 20 μm diameter and a wide range of liquid water contents. A study was also made to determine the effect of reducing the vapour source at infinity so that the droplets alone provided the vapour for particle growth. A parameterisation of ice particle growth rate is given as a function of liquid water content and ice particle and droplet sizes. These studies are of importance to considerations in thunderstorm electrification processes, where the mechanism of charge transfer between ice particles and graupel could take place.

  17. What controls the low ice number concentration in the upper troposphere?

    NASA Astrophysics Data System (ADS)

    Zhou, Cheng; Penner, Joyce E.; Lin, Guangxing; Liu, Xiaohong; Wang, Minghuai

    2016-10-01

    Cirrus clouds in the tropical tropopause play a key role in regulating the moisture entering the stratosphere through their dehydrating effect. Low ice number concentrations ( < 200 L-1) and high supersaturations (150-160 %) have been observed in these clouds. Different mechanisms have been proposed to explain these low ice number concentrations, including the inhibition of homogeneous freezing by the deposition of water vapour onto pre-existing ice crystals, heterogeneous ice formation on glassy organic aerosol ice nuclei (IN), and limiting the formation of ice number from high-frequency gravity waves. In this study, we examined the effect from three different representations of updraft velocities, the effect from pre-existing ice crystals, the effect from different water vapour deposition coefficients (α = 0.1 or 1), and the effect of 0.1 % of the total secondary organic aerosol (SOA) particles acting as IN. Model-simulated ice crystal numbers are compared against an aircraft observational dataset.Including the effect from water vapour deposition on pre-existing ice particles can effectively reduce simulated in-cloud ice number concentrations for all model setups. A larger water vapour deposition coefficient (α = 1) can also efficiently reduce ice number concentrations at temperatures below 205 K, but less so at higher temperatures. SOA acting as IN is most effective at reducing ice number concentrations when the effective updraft velocities are moderate ( ˜ 0.05-0.2 m s-1). However, the effects of including SOA as IN and using (α = 1) are diminished when the effect from pre-existing ice is included.When a grid-resolved large-scale updraft velocity ( < 0.1 m s-1) is used, the ice nucleation parameterization with homogeneous freezing only or with both homogeneous freezing and heterogeneous nucleation is able to generate low ice number concentrations in good agreement with observations for temperatures below 205 K as long as the pre-existing ice effect is

  18. What controls the low ice number concentration in the upper troposphere?

    NASA Astrophysics Data System (ADS)

    Zhou, C.; Penner, J. E.; Lin, G.; Liu, X.; Wang, M.

    2015-12-01

    Cirrus clouds in the tropical tropopause play a key role in regulating the moisture entering the stratosphere through their dehydrating effect. Low ice number concentrations (< 200 L-1) and high supersaturations (150-160 %) have been observed in these clouds. Different mechanisms have been proposed to explain these low ice number concentrations, including the inhibition of homogeneous freezing by the deposition of water vapour onto pre-existing ice crystals, heterogeneous ice formation on glassy organic aerosol ice nuclei (IN), and limiting the formation of ice number from high frequency gravity waves. In this study, we examined the effect from three different representations of updraft velocities, the effect from pre-existing ice crystals, the effect from different water vapour deposition coefficients (α = 0.1 or 1), and the effect of 0.1 % of the total secondary organic aerosol (SOA) particles acting as IN. Model simulated ice crystal numbers are compared against an aircraft observational dataset. Including the effect from water vapour deposition on pre-existing ice particles can effectively reduce simulated in-cloud ice number concentrations for all model set-ups. A larger water vapour deposition coefficient (α = 1) can also efficiently reduce ice number concentrations at temperatures below 205 K but less so at higher temperatures. SOA acting as IN are most effective at reducing ice number concentrations when the effective updraft velocities are moderate (∼ 0.05-0.2 m s-1). However, the effects of including SOA as IN and using (α = 1) are diminished when the effect from pre-existing ice is included. When a grid resolved large-scale updraft velocity (< 0.1 m s-1) is used, the ice nucleation parameterization with homogeneous freezing only or with both homogeneous freezing and heterogeneous nucleation is able to generate low ice number concentrations in good agreement with observations for temperatures below 205 K as long as the pre-existing ice effect is

  19. Retrieval of total water vapour in the Arctic using microwave humidity sounders

    NASA Astrophysics Data System (ADS)

    Cristian Scarlat, Raul; Melsheimer, Christian; Heygster, Georg

    2018-04-01

    Quantitative retrievals of atmospheric water vapour in the Arctic present numerous challenges because of the particular climate characteristics of this area. Here, we attempt to build upon the work of Melsheimer and Heygster (2008) to retrieve total atmospheric water vapour (TWV) in the Arctic from satellite microwave radiometers. While the above-mentioned algorithm deals primarily with the ice-covered central Arctic, with this work we aim to extend the coverage to partially ice-covered and ice-free areas. By using modelled values for the microwave emissivity of the ice-free sea surface, we develop two sub-algorithms using different sets of channels that deal solely with open-ocean areas. The new algorithm extends the spatial coverage of the retrieval throughout the year but especially in the warmer months when higher TWV values are frequent. The high TWV measurements over both sea-ice and open-water surfaces are, however, connected to larger uncertainties as the retrieval values are close to the instrument saturation limits.This approach allows us to apply the algorithm to regions where previously no data were available and ensures a more consistent physical analysis of the satellite measurements by taking into account the contribution of the surface emissivity to the measured signal.

  20. Southern Greenland water vapour isotopic composition at the crossroads of Atlantic and Arctic moisture

    NASA Astrophysics Data System (ADS)

    Bonne, J. L.; Steen-Larsen, H. C.; Risi, C. M.; Werner, M.; Sodemann, H.; Lacour, J. L.; Fettweis, X.; Cesana, G.; Delmotte, M.; Cattani, O.; Clerbaux, C.; Sveinbjörnsdottir, A. E.; Masson-Delmotte, V.

    2014-12-01

    Since September 2011, a continuous water vapour isotopic composition monitoring instrument has been remotely operated in Ivittuut (61.21°N, 48.17°W), southern Greenland. Meteorological parameters are monitored and precipitation has been sampled and analysed for isotopic composition, suggesting equilibrium between surface vapour and precipitation. The data depict small summer diurnal variations. δ18O and deuterium excess (d-excess) are generally anti-correlated and show important seasonal variations (with respective amplitudes of 10 and 20 ‰), and large synoptic variations associated to low-pressure systems (typically +5‰ on δ18O and -15‰ on d-excess). The moisture sources, estimated based on Lagrangian back-trajectories, are primarily influenced by the western North Atlantic, and north-eastern American continent. Notable are important seasonal and synoptic shifts of the moisture sources, and sporadic influences of the Arctic or the eastern North Atlantic. Moisture sources variations can be related to changes in water vapour isotopic composition, and the isotopic fingerprints can be attributed to the areas of moisture origins. Isotopic enabled AGCMs nudged to meteorology (LMDZiso, ECHAM5-wiso), despite biases, correctly capture the δ18O changes, but underestimate the d-excess changes. They allow to identify a high correlation between the southern Greenland d-excess and the simulated relative humidity and d-excess in the moisture source region south of Greenland. An extreme high temperature event in July 2012 affecting all Greenland, similar to ice sheet melt events during the medieval periods and one event in 1889 documented by Greenland ice core records, has been analysed regarding water vapour isotopic composition, using remote sensing (IASI) and in situ observations from Bermuda to northern Greenland (NEEM station). Our southern Greenland observations allow to track the water vapour evolution during this event along the moisture transport path

  1. Influence of glacial meltwater on global seawater δ234U

    NASA Astrophysics Data System (ADS)

    Arendt, Carli A.; Aciego, Sarah M.; Sims, Kenneth W. W.; Das, Sarah B.; Sheik, Cody; Stevenson, Emily I.

    2018-03-01

    We present the first published uranium-series measurements from modern Greenland Ice Sheet (GrIS) runoff and proximal seawater, and investigate the influence of glacial melt on global seawater δ234U over glacial-interglacial (g-ig) timescales. Climate reconstructions based on closed-system uranium-thorium (U/Th) dating of fossil corals assume U chemistry of seawater has remained stable over time despite notable fluctuations in major elemental compositions, concentrations, and isotopic compositions of global seawater on g-ig timescales. Deglacial processes increase weathering, significantly increasing U-series concentrations and changing the δ234U of glacial meltwater. Analyses of glacial discharge from GrIS outlet glaciers indicate that meltwater runoff has elevated U concentrations and differing 222Rn concentrations and δ234U compositions, likely due to variations in subglacial residence time. Locations with high δ234U have the potential to increase proximal seawater δ234U. To better understand the impact of bulk glacial melt on global seawater δ234U over time, we use a simple box model to scale these processes to periods of extreme deglaciation. We account for U fluxes from the GrIS, Antarctica, and large Northern Hemisphere Continental Ice Sheets, and assess sensitivity by varying melt volumes, duration and U flux input rates based on modern subglacial water U concentrations and compositions. All scenarios support the hypothesis that global seawater δ234U has varied by more than 1‰ through time as a function of predictable perturbations in continental U fluxes during g-ig periods.

  2. Organic matter controls of iron incorporation in growing sea ice

    NASA Astrophysics Data System (ADS)

    Janssens, Julie; Meiners, Klaus M.; Townsend, Ashley T.; Lannuzel, Delphine

    2018-03-01

    This study presents the first laboratory-controlled sea-ice growth experiment conducted under trace metal clean conditions. The role played by organic matter, in the incorporation of iron (Fe) into sea ice was investigated by means of laboratory ice-growth experiments using a titanium cold-finger apparatus. Experiments were also conducted to understand the role of extracellular polymeric substances (EPS) in the enrichment of ammonium in sea ice. Sea ice was grown from several seawater solutions containing different quantities and qualities of particulate Fe (PFe), dissolved Fe (DFe) and organic matter. Sea ice and seawater were analyzed for particulate organic carbon and nitrogen, macro-nutrients, extracellular EPS, PFe and DFe, and particulate aluminium. The experiments showed that biogenic PFe is preferentially incorporated into sea ice compared to lithogenic PFe. Furthermore, sea ice grown from ultra-violet (UV) and non-UV treated seawaters exhibits contrasting incorporation rates of organic matter and Fe. Whereas the effects of UV-treatments were not always significant, we do find indications that the type or organic matter controls the enrichment of Fe in forming sea ice.. Specifically, we come to the conclusion that the incorporation of DFe is favored by the presence of organic ligands in the source solution.

  3. Persistence of bacterial and archaeal communities in sea ice through an Arctic winter

    PubMed Central

    Collins, R Eric; Rocap, Gabrielle; Deming, Jody W

    2010-01-01

    The structure of bacterial communities in first-year spring and summer sea ice differs from that in source seawaters, suggesting selection during ice formation in autumn or taxon-specific mortality in the ice during winter. We tested these hypotheses by weekly sampling (January–March 2004) of first-year winter sea ice (Franklin Bay, Western Arctic) that experienced temperatures from −9°C to −26°C, generating community fingerprints and clone libraries for Bacteria and Archaea. Despite severe conditions and significant decreases in microbial abundance, no significant changes in richness or community structure were detected in the ice. Communities of Bacteria and Archaea in the ice, as in under-ice seawater, were dominated by SAR11 clade Alphaproteobacteria and Marine Group I Crenarchaeota, neither of which is known from later season sea ice. The bacterial ice library contained clones of Gammaproteobacteria from oligotrophic seawater clades (e.g. OM60, OM182) but no clones from gammaproteobacterial genera commonly detected in later season sea ice by similar methods (e.g. Colwellia, Psychrobacter). The only common sea ice bacterial genus detected in winter ice was Polaribacter. Overall, selection during ice formation and mortality during winter appear to play minor roles in the process of microbial succession that leads to distinctive spring and summer sea ice communities. PMID:20192970

  4. Exposed water ice on the nucleus of comet 67P/Churyumov-Gerasimenko.

    PubMed

    Filacchione, G; De Sanctis, M C; Capaccioni, F; Raponi, A; Tosi, F; Ciarniello, M; Cerroni, P; Piccioni, G; Capria, M T; Palomba, E; Bellucci, G; Erard, S; Bockelee-Morvan, D; Leyrat, C; Arnold, G; Barucci, M A; Fulchignoni, M; Schmitt, B; Quirico, E; Jaumann, R; Stephan, K; Longobardo, A; Mennella, V; Migliorini, A; Ammannito, E; Benkhoff, J; Bibring, J P; Blanco, A; Blecka, M I; Carlson, R; Carsenty, U; Colangeli, L; Combes, M; Combi, M; Crovisier, J; Drossart, P; Encrenaz, T; Federico, C; Fink, U; Fonti, S; Ip, W H; Irwin, P; Kuehrt, E; Langevin, Y; Magni, G; McCord, T; Moroz, L; Mottola, S; Orofino, V; Schade, U; Taylor, F; Tiphene, D; Tozzi, G P; Beck, P; Biver, N; Bonal, L; Combe, J-Ph; Despan, D; Flamini, E; Formisano, M; Fornasier, S; Frigeri, A; Grassi, D; Gudipati, M S; Kappel, D; Mancarella, F; Markus, K; Merlin, F; Orosei, R; Rinaldi, G; Cartacci, M; Cicchetti, A; Giuppi, S; Hello, Y; Henry, F; Jacquinod, S; Reess, J M; Noschese, R; Politi, R; Peter, G

    2016-01-21

    Although water vapour is the main species observed in the coma of comet 67P/Churyumov-Gerasimenko and water is the major constituent of cometary nuclei, limited evidence for exposed water-ice regions on the surface of the nucleus has been found so far. The absence of large regions of exposed water ice seems a common finding on the surfaces of many of the comets observed so far. The nucleus of 67P/Churyumov-Gerasimenko appears to be fairly uniformly coated with dark, dehydrated, refractory and organic-rich material. Here we report the identification at infrared wavelengths of water ice on two debris falls in the Imhotep region of the nucleus. The ice has been exposed on the walls of elevated structures and at the base of the walls. A quantitative derivation of the abundance of ice in these regions indicates the presence of millimetre-sized pure water-ice grains, considerably larger than in all previous observations. Although micrometre-sized water-ice grains are the usual result of vapour recondensation in ice-free layers, the occurrence of millimetre-sized grains of pure ice as observed in the Imhotep debris falls is best explained by grain growth by vapour diffusion in ice-rich layers, or by sintering. As a consequence of these processes, the nucleus can develop an extended and complex coating in which the outer dehydrated crust is superimposed on layers enriched in water ice. The stratigraphy observed on 67P/Churyumov-Gerasimenko is therefore the result of evolutionary processes affecting the uppermost metres of the nucleus and does not necessarily require a global layering to have occurred at the time of the comet's formation.

  5. Kinetics of ikaite precipitation and dissolution in seawater-derived brines at sub-zero temperatures to 265 K

    NASA Astrophysics Data System (ADS)

    Papadimitriou, Stathys; Kennedy, Hilary; Kennedy, Paul; Thomas, David N.

    2014-09-01

    The kinetics of calcium carbonate hexahydrate (ikaite) precipitation and dissolution were investigated in seawater and seawater-derived brines at sub-zero temperatures using the constant addition experimental technique. The steady state rate of these two processes was found to be a function of the deviation of the solution from equilibrium with respect to ikaite and conformed to the same empirical rate law as the anhydrous CaCO3 polymorphs, calcite and aragonite. In addition to the saturation state of the brine with respect to ikaite, the salinity of the brine and the temperature of the reaction evidently exerted some control on the ikaite precipitation kinetics, while the dissolution kinetics of the polymorph were not noticeably influenced by these two parameters. The experimental salinity and temperature conditions were equivalent to those at thermal equilibrium between brine and ice in the sea ice cover of polar seas. Simple modelling of the CO2 system by extrapolation of the oceanic equivalent to sea ice brines showed that the physical concentration of seawater ions and the changes in ikaite solubility as a function of salinity and temperature, both inherent in the sea ice system, would be insufficient to drive the emergent brines to ikaite supersaturation and precipitation in sea ice down to -8 °C. The loss of dissolved inorganic carbon to the gas phase of sea ice and to sympagic autotrophs are two independent mechanisms which, in nature, could prompt the brine CO2 system towards ikaite supersaturation and precipitation. Under these conditions, the steady state precipitation rate of ikaite was found to be fast enough for rapid formation within short time scales (days to weeks) in sea ice. The observed ikaite dissolution kinetics were also found conducive to short turn-over time scales of a few hours to a few days in corrosive solutions, such as surface seawater.

  6. Spring Melt and the Redistribution of Organochlorine Pesticides in the Sea-Ice Environment: A Comparative Study between Arctic and Antarctic Regions.

    PubMed

    Bigot, Marie; Hawker, Darryl W; Cropp, Roger; Muir, Derek Cg; Jensen, Bjarne; Bossi, Rossana; Bengtson Nash, Susan M

    2017-08-15

    Complementary sampling of air, snow, sea-ice, and seawater for a range of organochlorine pesticides (OCPs) was undertaken through the early stages of respective spring sea-ice melting at coastal sites in northeast Greenland and eastern Antarctica to investigate OCP concentrations and redistribution during this time. Mean concentrations in seawater, sea-ice and snow were generally greater at the Arctic site. For example, α-HCH was found to have the largest concentrations of all analytes in Arctic seawater and sea-ice meltwater samples (224-253 and 34.7-48.2 pg·L -1 respectively compared to 1.0-1.3 and <0.63 pg·L -1 respectively for Antarctic samples). Differences in atmospheric samples were generally not as pronounced however. Findings suggest that sea-ice OCP burdens originate from both snow and seawater. The distribution profile between seawater and sea-ice showed a compound-dependency for Arctic samples not evident with those from the Antarctic, possibly due to full submersion of sea-ice at the former. Seasonal sea-ice melt processes may alter the exchange rates of selected OCPs between air and seawater, but are not expected to reverse their direction, which fugacity modeling indicates is volatilisation in the Arctic and net deposition in the Antarctic. These predictions are consistent with the limited current observations.

  7. Bacterial community dynamics and activity in relation to dissolved organic matter availability during sea-ice formation in a mesocosm experiment.

    PubMed

    Eronen-Rasimus, Eeva; Kaartokallio, Hermanni; Lyra, Christina; Autio, Riitta; Kuosa, Harri; Dieckmann, Gerhard S; Thomas, David N

    2014-02-01

    The structure of sea-ice bacterial communities is frequently different from that in seawater. Bacterial entrainment in sea ice has been studied with traditional microbiological, bacterial abundance, and bacterial production methods. However, the dynamics of the changes in bacterial communities during the transition from open water to frozen sea ice is largely unknown. Given previous evidence that the nutritional status of the parent water may affect bacterial communities during ice formation, bacterial succession was studied in under ice water and sea ice in two series of mesocosms: the first containing seawater from the North Sea and the second containing seawater enriched with algal-derived dissolved organic matter (DOM). The composition and dynamics of bacterial communities were investigated with terminal restriction fragment length polymorphism (T-RFLP), and cloning alongside bacterial production (thymidine and leucine uptake) and abundance measurements (measured by flow cytometry). Enriched and active sea-ice bacterial communities developed in ice formed in both unenriched and DOM-enriched seawater (0-6 days). γ-Proteobacteria dominated in the DOM-enriched samples, indicative of their capability for opportunistic growth in sea ice. The bacterial communities in the unenriched waters and ice consisted of the classes Flavobacteria, α- and γ-Proteobacteria, which are frequently found in natural sea ice in polar regions. Furthermore, the results indicate that seawater bacterial communities are able to adapt rapidly to sudden environmental changes when facing considerable physicochemical stress such as the changes in temperature, salinity, nutrient status, and organic matter supply during ice formation. © 2014 The Authors. MicrobiologyOpen published by John Wiley & Sons Ltd.

  8. Floating ice-algal aggregates below melting arctic sea ice.

    PubMed

    Assmy, Philipp; Ehn, Jens K; Fernández-Méndez, Mar; Hop, Haakon; Katlein, Christian; Sundfjord, Arild; Bluhm, Katrin; Daase, Malin; Engel, Anja; Fransson, Agneta; Granskog, Mats A; Hudson, Stephen R; Kristiansen, Svein; Nicolaus, Marcel; Peeken, Ilka; Renner, Angelika H H; Spreen, Gunnar; Tatarek, Agnieszka; Wiktor, Jozef

    2013-01-01

    During two consecutive cruises to the Eastern Central Arctic in late summer 2012, we observed floating algal aggregates in the melt-water layer below and between melting ice floes of first-year pack ice. The macroscopic (1-15 cm in diameter) aggregates had a mucous consistency and were dominated by typical ice-associated pennate diatoms embedded within the mucous matrix. Aggregates maintained buoyancy and accumulated just above a strong pycnocline that separated meltwater and seawater layers. We were able, for the first time, to obtain quantitative abundance and biomass estimates of these aggregates. Although their biomass and production on a square metre basis was small compared to ice-algal blooms, the floating ice-algal aggregates supported high levels of biological activity on the scale of the individual aggregate. In addition they constituted a food source for the ice-associated fauna as revealed by pigments indicative of zooplankton grazing, high abundance of naked ciliates, and ice amphipods associated with them. During the Arctic melt season, these floating aggregates likely play an important ecological role in an otherwise impoverished near-surface sea ice environment. Our findings provide important observations and measurements of a unique aggregate-based habitat during the 2012 record sea ice minimum year.

  9. Floating Ice-Algal Aggregates below Melting Arctic Sea Ice

    PubMed Central

    Assmy, Philipp; Ehn, Jens K.; Fernández-Méndez, Mar; Hop, Haakon; Katlein, Christian; Sundfjord, Arild; Bluhm, Katrin; Daase, Malin; Engel, Anja; Fransson, Agneta; Granskog, Mats A.; Hudson, Stephen R.; Kristiansen, Svein; Nicolaus, Marcel; Peeken, Ilka; Renner, Angelika H. H.; Spreen, Gunnar; Tatarek, Agnieszka; Wiktor, Jozef

    2013-01-01

    During two consecutive cruises to the Eastern Central Arctic in late summer 2012, we observed floating algal aggregates in the melt-water layer below and between melting ice floes of first-year pack ice. The macroscopic (1-15 cm in diameter) aggregates had a mucous consistency and were dominated by typical ice-associated pennate diatoms embedded within the mucous matrix. Aggregates maintained buoyancy and accumulated just above a strong pycnocline that separated meltwater and seawater layers. We were able, for the first time, to obtain quantitative abundance and biomass estimates of these aggregates. Although their biomass and production on a square metre basis was small compared to ice-algal blooms, the floating ice-algal aggregates supported high levels of biological activity on the scale of the individual aggregate. In addition they constituted a food source for the ice-associated fauna as revealed by pigments indicative of zooplankton grazing, high abundance of naked ciliates, and ice amphipods associated with them. During the Arctic melt season, these floating aggregates likely play an important ecological role in an otherwise impoverished near-surface sea ice environment. Our findings provide important observations and measurements of a unique aggregate-based habitat during the 2012 record sea ice minimum year. PMID:24204642

  10. TOPICAL REVIEW: Sintering and microstructure of ice: a review

    NASA Astrophysics Data System (ADS)

    Blackford, Jane R.

    2007-11-01

    Sintering of ice is driven by the thermodynamic requirement to decrease surface energy. The structural morphology of ice in nature has many forms—from snowflakes to glaciers. These forms and their evolution depend critically on the balance between the thermodynamic and kinetic factors involved. Ice is a crystalline material so scientific understanding and approaches from more conventional materials can be applied to ice. The early models of solid state ice sintering are based on power law models originally developed in metallurgy. For pressure sintering of ice, these are based on work on hot isostatic pressing of metals and ceramics. Recent advances in recognizing the grain boundary groove geometry between sintering ice particles require models that use new approaches in materials science. The newer models of sintering in materials science are beginning to incorporate more realistic processing conditions and microstructural complexity, and so there is much to be gained from applying these to ice in the future. The vapour pressure of ice is high, which causes it to sublime readily. The main mechanism for isothermal sintering of ice particles is by vapour diffusion; however other transport mechanisms certainly contribute. Plastic deformation with power law creep combined with recrystallization become important mechanisms in sintering with external pressure. Modern experimental techniques, low temperature scanning electron microscopy and x-ray tomography, are providing new insights into the evolution of microstructures in ice. Sintering in the presence of a small volume fraction of the liquid phase causes much higher bond growth rates. This may be important in natural snow which contains impurities that form a liquid phase. Knowledge of ice microstructure and sintering is beneficial in understanding mechanical behaviour in ice friction and the stability of snow slopes prone to avalanches.

  11. Invisible polynyas: Modulation of fast ice thickness by ocean heat flux on the Canadian polar shelf

    NASA Astrophysics Data System (ADS)

    Melling, Humfrey; Haas, Christian; Brossier, Eric

    2015-02-01

    Although the Canadian polar shelf is dominated by thick fast ice in winter, areas of young ice or open water do recur annually at locations within and adjacent to the fast ice. These polynyas are detectable by eye and sustained by wind or tide-driven ice divergence and ocean heat flux. Our ice-thickness surveys by drilling and towed electromagnetic sounder reveal that visible polynyas comprise only a subset of thin-ice coverage. Additional area in the coastal zone, in shallow channels and in fjords is covered by thin ice which is too thick to be discerned by eye. Our concurrent surveys by CTD reveal correlation between thin fast ice and above-freezing seawater beneath it. We use winter time series of air and ocean temperatures and ice and snow thicknesses to calculate the ocean-to-ice heat flux as 15 and 22 W/m2 at locations with thin ice in Penny Strait and South Cape Fjord, respectively. Near-surface seawater above freezing is not a sufficient condition for ocean heat to reach the ice; kinetic energy is needed to overcome density stratification. The ocean's isolation from wind under fast ice in winter leaves tides as the only source. Two tidal mechanisms driving ocean heat flux are discussed: diffusion via turbulence generated by shear at the under-ice and benthic boundaries, and the internal hydraulics of flow over topography. The former appears dominant in channels and the coastal zone and the latter in some silled fjords where and when the layering of seawater density permits hydraulically critical flow.

  12. Ice nucleation active particles are efficiently removed by precipitating clouds.

    PubMed

    Stopelli, Emiliano; Conen, Franz; Morris, Cindy E; Herrmann, Erik; Bukowiecki, Nicolas; Alewell, Christine

    2015-11-10

    Ice nucleation in cold clouds is a decisive step in the formation of rain and snow. Observations and modelling suggest that variations in the concentrations of ice nucleating particles (INPs) affect timing, location and amount of precipitation. A quantitative description of the abundance and variability of INPs is crucial to assess and predict their influence on precipitation. Here we used the hydrological indicator δ(18)O to derive the fraction of water vapour lost from precipitating clouds and correlated it with the abundance of INPs in freshly fallen snow. Results show that the number of INPs active at temperatures ≥ -10 °C (INPs-10) halves for every 10% of vapour lost through precipitation. Particles of similar size (>0.5 μm) halve in number for only every 20% of vapour lost, suggesting effective microphysical processing of INPs during precipitation. We show that INPs active at moderate supercooling are rapidly depleted by precipitating clouds, limiting their impact on subsequent rainfall development in time and space.

  13. The impact of dissolved organic carbon and bacterial respiration on pCO2 in experimental sea ice

    NASA Astrophysics Data System (ADS)

    Zhou, J.; Kotovitch, M.; Kaartokallio, H.; Moreau, S.; Tison, J.-L.; Kattner, G.; Dieckmann, G.; Thomas, D. N.; Delille, B.

    2016-02-01

    Previous observations have shown that the partial pressure of carbon dioxide (pCO2) in sea ice brines is generally higher in Arctic sea ice compared to those from the Antarctic sea ice, especially in winter and early spring. We hypothesized that these differences result from the higher dissolved organic carbon (DOC) content in Arctic seawater: Higher concentrations of DOC in seawater would be reflected in a greater DOC incorporation into sea ice, enhancing bacterial respiration, which in turn would increase the pCO2 in the ice. To verify this hypothesis, we performed an experiment using two series of mesocosms: one was filled with seawater (SW) and the other one with seawater with an addition of filtered humic-rich river water (SWR). The addition of river water increased the DOC concentration of the water from a median of 142 μmol Lwater-1 in SW to 249 μmol Lwater-1 in SWR. Sea ice was grown in these mesocosms under the same physical conditions over 19 days. Microalgae and protists were absent, and only bacterial activity has been detected. We measured the DOC concentration, bacterial respiration, total alkalinity and pCO2 in sea ice and the underlying seawater, and we calculated the changes in dissolved inorganic carbon (DIC) in both media. We found that bacterial respiration in ice was higher in SWR: median bacterial respiration was 25 nmol C Lice-1 h-1 compared to 10 nmol C Lice-1 h-1 in SW. pCO2 in ice was also higher in SWR with a median of 430 ppm compared to 356 ppm in SW. However, the differences in pCO2 were larger within the ice interiors than at the surfaces or the bottom layers of the ice, where exchanges at the air-ice and ice-water interfaces might have reduced the differences. In addition, we used a model to simulate the differences of pCO2 and DIC based on bacterial respiration. The model simulations support the experimental findings and further suggest that bacterial growth efficiency in the ice might approach 0.15 and 0.2. It is thus credible

  14. Methane excess in Arctic surface water-triggered by sea ice formation and melting.

    PubMed

    Damm, E; Rudels, B; Schauer, U; Mau, S; Dieckmann, G

    2015-11-10

    Arctic amplification of global warming has led to increased summer sea ice retreat, which influences gas exchange between the Arctic Ocean and the atmosphere where sea ice previously acted as a physical barrier. Indeed, recently observed enhanced atmospheric methane concentrations in Arctic regions with fractional sea-ice cover point to unexpected feedbacks in cycling of methane. We report on methane excess in sea ice-influenced water masses in the interior Arctic Ocean and provide evidence that sea ice is a potential source. We show that methane release from sea ice into the ocean occurs via brine drainage during freezing and melting i.e. in winter and spring. In summer under a fractional sea ice cover, reduced turbulence restricts gas transfer, then seawater acts as buffer in which methane remains entrained. However, in autumn and winter surface convection initiates pronounced efflux of methane from the ice covered ocean to the atmosphere. Our results demonstrate that sea ice-sourced methane cycles seasonally between sea ice, sea-ice-influenced seawater and the atmosphere, while the deeper ocean remains decoupled. Freshening due to summer sea ice retreat will enhance this decoupling, which restricts the capacity of the deeper Arctic Ocean to act as a sink for this greenhouse gas.

  15. Caldera unrest detected with seawater temperature anomalies at Deception Island, Antarctic Peninsula

    NASA Astrophysics Data System (ADS)

    Berrocoso, M.; Prates, G.; Fernández-Ros, A.; Peci, L. M.; de Gil, A.; Rosado, B.; Páez, R.; Jigena, B.

    2018-04-01

    Increased thermal activity was detected to coincide with the onset of volcano inflation in the seawater-filled caldera at Deception Island. This thermal activity was manifested in pulses of high water temperature that coincided with ocean tide cycles. The seawater temperature anomalies were detected by a thermometric sensor attached to the tide gauge (bottom pressure sensor). This was installed where the seawater circulation and the locations of known thermal anomalies, fumaroles and thermal springs, together favor the detection of water warmed within the caldera. Detection of the increased thermal activity was also possible because sea ice, which covers the entire caldera during the austral winter months, insulates the water and thus reduces temperature exchange between seawater and atmosphere. In these conditions, the water temperature data has been shown to provide significant information about Deception volcano activity. The detected seawater temperature increase, also observed in soil temperature readings, suggests rapid and near-simultaneous increase in geothermal activity with onset of caldera inflation and an increased number of seismic events observed in the following austral summer.

  16. Experimental evidence for carbonate precipitation and CO 2 degassing during sea ice formation

    NASA Astrophysics Data System (ADS)

    Papadimitriou, S.; Kennedy, H.; Kattner, G.; Dieckmann, G. S.; Thomas, D. N.

    2004-04-01

    Chemical and stable carbon isotopic modifications during the freezing of artificial seawater were measured in four 4 m 3 tank incubations. Three of the four incubations were inoculated with a nonaxenic Antarctic diatom culture. The 18 days of freezing resulted in 25 to 27 cm thick ice sheets overlying the residual seawater. The ice phase was characterized by a decrease in temperature from -1.9 to -2.2°C in the under-ice seawater down to -6.7°C in the upper 4 cm of the ice sheet, with a concurrent increase in the salinity of the under-ice seawater and brine inclusions of the ice sheet as a result of physical concentration of major dissolved salts by expulsion from the solid ice matrix. Measurements of pH, total dissolved inorganic carbon (C T) and its stable isotopic composition (δ 13C T) all exhibited changes, which suggest minimal effect by biological activity during the experiment. A systematic drop in pH and salinity-normalized C T by up to 0.37 pH SWS units and 376 μmol C kg -1 respectively at the lowest temperature and highest salinity part of the ice sheet were coupled with an equally systematic 13C enrichment of the C T. Calculations based on the direct pH and C T measurements indicated a steady increase in the in situ concentration of dissolved carbon dioxide (CO 2(aq)) with time and increasing salinity within the ice sheet, partly due to changes in the dissociation constants of carbonic acid in the low temperature-high salinity range within sea ice. The combined effects of temperature and salinity on the solubility of CO 2 over the range of conditions encountered during this study was a slight net decrease in the equilibrium CO 2(aq) concentration as a result of the salting-out overriding the increase in solubility with decreasing temperature. Hence, the increase in the in situ CO 2(aq) concentration lead to saturation or supersaturation of the brine inclusions in the ice sheet with respect to atmospheric pCO 2 (≈3.5 × 10 -4 atm). When all physico

  17. Archival processes of the water stable isotope signal in East Antarctic ice cores

    NASA Astrophysics Data System (ADS)

    Casado, Mathieu; Landais, Amaelle; Picard, Ghislain; Münch, Thomas; Laepple, Thomas; Stenni, Barbara; Dreossi, Giuliano; Ekaykin, Alexey; Arnaud, Laurent; Genthon, Christophe; Touzeau, Alexandra; Masson-Delmotte, Valerie; Jouzel, Jean

    2018-05-01

    The oldest ice core records are obtained from the East Antarctic Plateau. Water isotopes are key proxies to reconstructing past climatic conditions over the ice sheet and at the evaporation source. The accuracy of climate reconstructions depends on knowledge of all processes affecting water vapour, precipitation and snow isotopic compositions. Fractionation processes are well understood and can be integrated in trajectory-based Rayleigh distillation and isotope-enabled climate models. However, a quantitative understanding of processes potentially altering snow isotopic composition after deposition is still missing. In low-accumulation sites, such as those found in East Antarctica, these poorly constrained processes are likely to play a significant role and limit the interpretability of an ice core's isotopic composition. By combining observations of isotopic composition in vapour, precipitation, surface snow and buried snow from Dome C, a deep ice core site on the East Antarctic Plateau, we found indications of a seasonal impact of metamorphism on the surface snow isotopic signal when compared to the initial precipitation. Particularly in summer, exchanges of water molecules between vapour and snow are driven by the diurnal sublimation-condensation cycles. Overall, we observe in between precipitation events modification of the surface snow isotopic composition. Using high-resolution water isotopic composition profiles from snow pits at five Antarctic sites with different accumulation rates, we identified common patterns which cannot be attributed to the seasonal variability of precipitation. These differences in the precipitation, surface snow and buried snow isotopic composition provide evidence of post-deposition processes affecting ice core records in low-accumulation areas.

  18. Cubic ice and large humidity with respect to ice in cold cirrus clouds

    NASA Astrophysics Data System (ADS)

    Bogdan, A.; Loerting, T.

    2009-04-01

    Recently several studies have reported about the possible formation of cubic ice in upper-tropospheric cirrus ice clouds and its role in the observed elevated relative humidity with respect to hexagonal ice, RHi, within the clouds. Since cubic ice is metastable with respect to stable hexagonal ice, its vapour pressure is higher. A key issue in determining the ratio of vapour pressures of cubic ice Pc and hexagonal ice Ph is the enthalpy of transformation from cubic to hexagonal ice Hc→h. By dividing the two integrated forms of the Clausius-Clapeyron equation for cubic ice and hexagonal ice, one obtains the relationship (1): ln Pc-- ln P*c-=--(Hc→h--) Ph P*h R 1T-- 1T* (1) from which the importance of Hc→h is evident. In many literature studies the approximation (2) is used: ln Pc-= Hc-→h. Ph RT (2) Using this approximated form one can predict the ratio of vapour pressures by measuring Hc→h. Unfortunately, the measurement of Hc→h is difficult. First, the enthalpy difference is very small, and the transition takes place over a broad temperature range, e.g., between 230 K and 260 K in some of our calorimetry experiments. Second, cubic ice (by contrast to hexagonal ice) can not be produced as a pure crystal. It always contains hexagonal stacking faults, which are evidenced by the (111)-hexagonal Bragg peak in the powder diffractogram. If the number of hexagonal stacking faults in cubic ice is high, then one could even consider this material as hexagonal ice with cubic stacking faults. Using the largest literature value of the change of enthalpy of transformation from cubic to hexagonal ice, Hc→h ? 160 J/mol, Murphy and Koop (2005) calculated that Pc would be ~10% higher than that of hexagonal ice Phat 180 K - 190 K, which agrees with the measurements obtained later by Shilling et al. (2006). Based on this result Shilling et al. concluded that "the formation of cubic ice at T < 202 K may significantly contribute to the persistent in

  19. The effects of snow and salt on ice table stability in University Valley, Antarctica

    USGS Publications Warehouse

    Williams, Kaj; Heldmann, Jennifer L.; McKay, Christopher P.; Mellon, Michael T.

    2018-01-01

    The Antarctic Dry Valleys represent a unique environment where it is possible to study dry permafrost overlaying an ice-rich permafrost. In this paper, two opposing mechanisms for ice table stability in University Valley are addressed: i) diffusive recharge via thin seasonal snow deposits and ii) desiccation via salt deposits in the upper soil column. A high-resolution time-marching soil and snow model was constructed and applied to University Valley, driven by meteorological station atmospheric measurements. It was found that periodic thin surficial snow deposits (observed in University Valley) are capable of drastically slowing (if not completely eliminating) the underlying ice table ablation. The effects of NaCl, CaCl2 and perchlorate deposits were then modelled. Unlike the snow cover, however, the presence of salt in the soil surface (but no periodic snow) results in a slight increase in the ice table recession rate, due to the hygroscopic effects of salt sequestering vapour from the ice table below. Near-surface pore ice frequently forms when large amounts of salt are present in the soil due to the suppression of the saturation vapour pressure. Implications for Mars high latitudes are discussed.

  20. Triple Oxygen Isotope Constraints on Seawater δ18O and Temperature

    NASA Astrophysics Data System (ADS)

    Hayles, J.; Shen, B.; Homann, M.; Yeung, L.

    2017-12-01

    One point of contention among geoscientists is whether the 18O/16O ratio of seawater is roughly constant, or if it varies considerably throughout geologic time. On one hand, the oxygen isotope composition of the ocean is thought to be well buffered by high- and low-temperature interactions between seawater and seafloor rocks. If these interactions do not vary on billion-year timescales, the oxygen-isotope compositions of marine sedimentary rocks mostly relate to changes in seawater temperature and global ice volume. On the other hand, long-term cooling of the planetary interior would alter these water-rock interactions leading to a secular change in the oxygen isotope composition of seawater. Models suggest that this secular change would enrich seawater with heavy oxygen isotopes over time. In this study, we present new, high precision, triple-oxygen-isotope (18O/16O, 17O/16O) analyses of marine chert samples from 3.45 Ga to 460Ma. The results of these analyses are paired with a new theoretical quartz-water equilibrium curve and a simplified seawater model to provide possible pairings of δ'18O and Δ'17O for the water which these samples could have formed in equilibrium with. Analysis of the new sample data, in addition to published chert triple oxygen isotope compositions, shows a general trend of older chert samples being progressively incompatible with waters possessing a modern-like seawater triple oxygen isotope composition. Implications on constraining the secular evolution of seawater δ18O and temperature will be discussed.

  1. Modelling and intepreting the isotopic composition of water vapour in convective updrafts

    NASA Astrophysics Data System (ADS)

    Bolot, M.; Legras, B.; Moyer, E. J.

    2012-08-01

    The isotopic compositions of water vapour and its condensates have long been used as tracers of the global hydrological cycle, but may also be useful for understanding processes within individual convective clouds. We review here the representation of processes that alter water isotopic compositions during processing of air in convective updrafts and present a unified model for water vapour isotopic evolution within undiluted deep convective cores, with a special focus on the out-of-equilibrium conditions of mixed phase zones where metastable liquid water and ice coexist. We use our model to show that a combination of water isotopologue measurements can constrain critical convective parameters including degree of supersaturation, supercooled water content and glaciation temperature. Important isotopic processes in updrafts include kinetic effects that are a consequence of diffusive growth or decay of cloud particles within a supersaturated or subsaturated environment; isotopic re-equilibration between vapour and supercooled droplets, which buffers isotopic distillation; and differing mechanisms of glaciation (droplet freezing vs. the Wegener-Bergeron-Findeisen process). As all of these processes are related to updraft strength, droplet size distribution and the retention of supercooled water, isotopic measurements can serve as a probe of in-cloud conditions of importance to convective processes. We study the sensitivity of the profile of water vapour isotopic composition to differing model assumptions and show how measurements of isotopic composition at cloud base and cloud top alone may be sufficient to retrieve key cloud parameters.

  2. Modelling and interpreting the isotopic composition of water vapour in convective updrafts

    NASA Astrophysics Data System (ADS)

    Bolot, M.; Legras, B.; Moyer, E. J.

    2013-08-01

    The isotopic compositions of water vapour and its condensates have long been used as tracers of the global hydrological cycle, but may also be useful for understanding processes within individual convective clouds. We review here the representation of processes that alter water isotopic compositions during processing of air in convective updrafts and present a unified model for water vapour isotopic evolution within undiluted deep convective cores, with a special focus on the out-of-equilibrium conditions of mixed-phase zones where metastable liquid water and ice coexist. We use our model to show that a combination of water isotopologue measurements can constrain critical convective parameters, including degree of supersaturation, supercooled water content and glaciation temperature. Important isotopic processes in updrafts include kinetic effects that are a consequence of diffusive growth or decay of cloud particles within a supersaturated or subsaturated environment; isotopic re-equilibration between vapour and supercooled droplets, which buffers isotopic distillation; and differing mechanisms of glaciation (droplet freezing vs. the Wegener-Bergeron-Findeisen process). As all of these processes are related to updraft strength, particle size distribution and the retention of supercooled water, isotopic measurements can serve as a probe of in-cloud conditions of importance to convective processes. We study the sensitivity of the profile of water vapour isotopic composition to differing model assumptions and show how measurements of isotopic composition at cloud base and cloud top alone may be sufficient to retrieve key cloud parameters.

  3. Ice Particle Growth Rates Under Upper Troposphere Conditions

    NASA Technical Reports Server (NTRS)

    Peterson, Harold; Bailey, Matthew; Hallett, John

    2010-01-01

    Atmospheric conditions for growth of ice crystals (temperature and ice supersaturation) are often not well constrained and it is necessary to simulate such conditions in the laboratory to investigate such growth under well controlled conditions over many hours. The growth of ice crystals from the vapour in both prism and basal planes was observed at temperatures of -60 C and -70 C under ice supersaturation up to 100% (200% relative humidity) at pressures derived from the standard atmosphere in a static diffusion chamber. Crystals grew outward from a vertical glass filament, thickening in the basal plane by addition of macroscopic layers greater than 2 m, leading to growth in the prism plane by passing of successive layers conveniently viewed by time lapse video.

  4. Ice Crystal Growth Rates Under Upper Troposphere Conditions

    NASA Technical Reports Server (NTRS)

    Peterson, Harold S.; Bailey, Matthew; Hallett, John

    2010-01-01

    Atmospheric conditions for growth of ice crystals (temperature and ice supersaturation) are often not well constrained and it is necessary to simulate such conditions in the laboratory to investigate such growth under well controlled conditions over many hours. The growth of ice crystals from the vapour in both prism and basal planes was observed at temperatures of -60 C and -70 C under ice supersaturation up to 100% (200% relative humidity) at pressures derived from the standard atmosphere in a static diffusion chamber. Crystals grew outward from a vertical glass filament, thickening in the basal plane by addition of macroscopic layers greater than 2 m, leading to growth in the prism plane by passing of successive layers conveniently viewed by time lapse video.

  5. Square ice in graphene nanocapillaries.

    PubMed

    Algara-Siller, G; Lehtinen, O; Wang, F C; Nair, R R; Kaiser, U; Wu, H A; Geim, A K; Grigorieva, I V

    2015-03-26

    Bulk water exists in many forms, including liquid, vapour and numerous crystalline and amorphous phases of ice, with hexagonal ice being responsible for the fascinating variety of snowflakes. Much less noticeable but equally ubiquitous is water adsorbed at interfaces and confined in microscopic pores. Such low-dimensional water determines aspects of various phenomena in materials science, geology, biology, tribology and nanotechnology. Theory suggests many possible phases for adsorbed and confined water, but it has proved challenging to assess its crystal structure experimentally. Here we report high-resolution electron microscopy imaging of water locked between two graphene sheets, an archetypal example of hydrophobic confinement. The observations show that the nanoconfined water at room temperature forms 'square ice'--a phase having symmetry qualitatively different from the conventional tetrahedral geometry of hydrogen bonding between water molecules. Square ice has a high packing density with a lattice constant of 2.83 Å and can assemble in bilayer and trilayer crystallites. Molecular dynamics simulations indicate that square ice should be present inside hydrophobic nanochannels independently of their exact atomic nature.

  6. Square ice in graphene nanocapillaries

    NASA Astrophysics Data System (ADS)

    Algara-Siller, G.; Lehtinen, O.; Wang, F. C.; Nair, R. R.; Kaiser, U.; Wu, H. A.; Geim, A. K.; Grigorieva, I. V.

    2015-03-01

    Bulk water exists in many forms, including liquid, vapour and numerous crystalline and amorphous phases of ice, with hexagonal ice being responsible for the fascinating variety of snowflakes. Much less noticeable but equally ubiquitous is water adsorbed at interfaces and confined in microscopic pores. Such low-dimensional water determines aspects of various phenomena in materials science, geology, biology, tribology and nanotechnology. Theory suggests many possible phases for adsorbed and confined water, but it has proved challenging to assess its crystal structure experimentally. Here we report high-resolution electron microscopy imaging of water locked between two graphene sheets, an archetypal example of hydrophobic confinement. The observations show that the nanoconfined water at room temperature forms `square ice'--a phase having symmetry qualitatively different from the conventional tetrahedral geometry of hydrogen bonding between water molecules. Square ice has a high packing density with a lattice constant of 2.83 Å and can assemble in bilayer and trilayer crystallites. Molecular dynamics simulations indicate that square ice should be present inside hydrophobic nanochannels independently of their exact atomic nature.

  7. Possible precipitation of ice at low latitudes of Mars during periods of high obliquity

    USGS Publications Warehouse

    Jakosky, B.M.; Carr, M.H.

    1985-01-01

    Most of the old cratered highlands of Mars are dissected by branching river valleys that appear to have been cut by running water1,2 yet liquid water is unstable everywhere on the martian surface. In the equatorial region, where most of the valleys are observed, even ice is unstable3,4. It has been suggested, therefore, that Mars had an early denser atmosphere with sufficient greenhouse warming to allow the existence of liquid water 5. Here, we suggest instead that during periods of very high obliquities, ice could accumulate at low latitudes as a result of sustained sublimation of ice from the poles and transport of the water vapour equatorwards. At low latitudes, the water vapour would saturate the atmosphere and condense onto the surface where it would accumulate until lower obliquities prevailed. The mechanism is efficient only at the very high obliquities that occurred before formation of Tharsis very early in the planet's history, but limited equatorial ice accumulation could also have occurred at the highest obliquities during the rest of the planet's history. Partial melting of the ice could have provided runoff to form the channels or replenish the groundwater system. ?? 1985 Nature Publishing Group.

  8. Multiphase Reactive Transport and Platelet Ice Accretion in the Sea Ice of McMurdo Sound, Antarctica

    NASA Astrophysics Data System (ADS)

    Buffo, J. J.; Schmidt, B. E.; Huber, C.

    2018-01-01

    Sea ice seasonally to interannually forms a thermal, chemical, and physical boundary between the atmosphere and hydrosphere over tens of millions of square kilometers of ocean. Its presence affects both local and global climate and ocean dynamics, ice shelf processes, and biological communities. Accurate incorporation of sea ice growth and decay, and its associated thermal and physiochemical processes, is underrepresented in large-scale models due to the complex physics that dictate oceanic ice formation and evolution. Two phenomena complicate sea ice simulation, particularly in the Antarctic: the multiphase physics of reactive transport brought about by the inhomogeneous solidification of seawater, and the buoyancy driven accretion of platelet ice formed by supercooled ice shelf water onto the basal surface of the overlying ice. Here a one-dimensional finite difference model capable of simulating both processes is developed and tested against ice core data. Temperature, salinity, liquid fraction, fluid velocity, total salt content, and ice structure are computed during model runs. The model results agree well with empirical observations and simulations highlight the effect platelet ice accretion has on overall ice thickness and characteristics. Results from sensitivity studies emphasize the need to further constrain sea ice microstructure and the associated physics, particularly permeability-porosity relationships, if a complete model of sea ice evolution is to be obtained. Additionally, implications for terrestrial ice shelves and icy moons in the solar system are discussed.

  9. Ice Particle Growth Under Conditions of the Upper Troposphere

    NASA Technical Reports Server (NTRS)

    Peterson, Harold S.; Bailey, Matthew; Hallett, John

    2010-01-01

    Atmospheric conditions for growth of ice crystals (temperature and ice supersaturation) are often not well constrained and it is necessary to simulate such conditions in the laboratory to investigate such growth under well controlled conditions over many hours. The growth of ice crystals from the vapour in both prism and basal planes was observed at temperatures of -60 C and -70 C under ice supersaturation up to 100% (200% relative humidity) at pressures derived from the standard atmosphere in a static diffusion chamber. Crystals grew outward from a vertical glass filament, thickening in the basal plane by addition of macroscopic layers greater than 2 microns, leading to growth in the prism plane by passing of successive layers conveniently viewed by time lapse video.

  10. Major new sources of biological ice nuclei

    NASA Astrophysics Data System (ADS)

    Moffett, B. F.; Hill, T.; Henderson-Begg, S. K.

    2009-12-01

    Almost all research on biological ice nucleation has focussed on a limited number of bacteria. Here we characterise several major new sources of biogenic ice nuclei. These include mosses, hornworts, liverworts and cyanobacteria. Ice nucleation in the eukaryotic bryophytes appears to be ubiquitous. The temperature at which these organisms nucleate is that at which the difference in vapour pressure over ice and water is at or close to its maximum. At these temperatures (-8 to -18 degrees C) ice will grow at the expense of supercooled water. These organisms are dependent for their water on occult precipitation - fog, dew and cloudwater which by its nature is not collected in conventional rain gauges. Therefore we suggest that these organism produce ice nuclei as a water harvesting mechanism. Since the same mechanism would also drive the Bergeron-Findeisen process, and as moss is known to become airborne, these nuclei may have a role in the initiation of precipitation. The properties of these ice nuclei are very different from the well characterised bacterial nuclei. We will also present DNA sequence data showing that, although related, the proteins responsible are only very distantly related to the classical bacterial ice nuclei.

  11. Arctic multiyear ice classification and summer ice cover using passive microwave satellite data

    NASA Astrophysics Data System (ADS)

    Comiso, J. C.

    1990-08-01

    The ability to classify and monitor Arctic multiyear sea ice cover using multispectral passive microwave data is studied. Sea ice concentration maps during several summer minima have been analyzed to obtain estimates of ice surviving the summer. The results are compared with multiyear ice concentrations derived from data the following winter, using an algorithm that assumes a certain emissivity for multiyear ice. The multiyear ice cover inferred from the winter data is approximately 25 to 40% less than the summer ice cover minimum, suggesting that even during winter when the emissivity of sea ice is most stable, passive microwave data may account for only a fraction of the total multiyear ice cover. The difference of about 2×106 km2 is considerably more than estimates of advection through Fram Strait during the intervening period. It appears that as in the Antarctic, some multiyear ice floes in the Arctic, especially those near the summer marginal ice zone, have first-year ice or intermediate signatures in the subsequent winter. A likely mechanism for this is the intrusion of seawater into the snow-ice interface, which often occurs near the marginal ice zone or in areas where snow load is heavy. Spatial variations in melt and melt ponding effects also contribute to the complexity of the microwave emissivity of multiyear ice. Hence the multiyear ice data should be studied in conjunction with the previous summer ice data to obtain a more complete characterization of the state of the Arctic ice cover. The total extent and actual areas of the summertime Arctic pack ice were estimated to be 8.4×106 km2 and 6.2×106 km2, respectively, and exhibit small interannual variability during the years 1979 through 1985, suggesting a relatively stable ice cover.

  12. Ice-Shelf Tidal Flexure and Subglacial Pressure Variations

    NASA Technical Reports Server (NTRS)

    Walker, Ryan T.; Parizek, Byron R.; Alley, Richard B.; Anandakrishnan, Sridhar; Riverman, Kiya L.; Christianson, Knut

    2013-01-01

    We develop a model of an ice shelf-ice stream system as a viscoelastic beam partially supported by an elastic foundation. When bed rock near the grounding line acts as a fulcrum, leverage from the ice shelf dropping at low tide can cause significant (approx 1 cm) uplift in the first few kilometers of grounded ice.This uplift and the corresponding depression at high tide lead to basal pressure variations of sufficient magnitude to influence subglacial hydrology.Tidal flexure may thus affect basal lubrication, sediment flow, and till strength, all of which are significant factors in ice-stream dynamics and grounding-line stability. Under certain circumstances, our results suggest the possibility of seawater being drawn into the subglacial water system. The presence of sea water beneath grounded ice would significantly change the radar reflectivity of the grounding zone and complicate the interpretation of grounded versus floating ice based on ice-penetrating radar observations.

  13. FU Orionis outbursts, preferential recondensation of water ice, and the formation of giant planets

    NASA Astrophysics Data System (ADS)

    Hubbard, Alexander

    2017-02-01

    Ices, including water ice, prefer to recondense on to preexisting nuclei rather than spontaneously forming grains from a cloud of vapour. Interestingly, different potential recondensation nuclei have very different propensities to actually nucleate water ice at the temperatures associated with freeze-out in protoplanetary discs. Therefore, if a region in a disc is warmed and then recooled, water vapour should not be expected to refreeze evenly on to all available grains. Instead, it will preferentially recondense on to the most favorable grains. When the recooling is slow enough, only the most favorable grains will nucleate ice, allowing them to recondense thick ice mantles. We quantify the conditions for preferential recondensation to rapidly create pebble-sized grains in protoplanetary discs and show that FU Orionis type outbursts have the appropriate cooling rates to drive pebble creation in a band about 5 au wide outside of the quiescent frost line from approximately Jupiter's orbit to Saturn's (about -10 au). Those pebbles could be of the appropriate size to proceed to planetesimal formation via the Streaming Instability, or to contribute to the growth of planetesimals through pebble accretion. We suggest that this phenomenon contributed to the formation of the gas giants in our own Solar system.

  14. The ESA DUE GlobVapour Project

    NASA Astrophysics Data System (ADS)

    Schröder, M.; ESA Due Globvapour Project Team

    2010-12-01

    The European Space Agency (ESA) Data User Element (DUE) project series aims at bridging the gap between research projects and the sustainable provision of Earth Observation (EO) climate data products at an information level that fully responds to the operational needs of user communities. The ultimate objective of GlobVapour is to provide long-term coherent water vapour data sets exploiting the synergistic capabilities of different EO missions aiming at improved accuracies and enhanced temporal and spatial sampling better than those provided by the single sources. The project seeks to utilize the increasing potential of the synergistic capabilities of past, existing and upcoming satellite missions (ERS-1 and -2, ENVISAT, METOP, MSG as well as relevant non-European missions and in-situ data) in order to meet the increasing needs for coherent long-term water vapour datasets required by the scientific community. GlobVapour develops, validates and applies novel water vapour climate data sets derived from various sensors. More specifically, the primary objectives of the GlobVapour project are: 1)The development of multi-annual global water vapour data sets inclusive of error estimates based on carefully calibrated and inter-calibrated radiances. 2)The validation of the water vapour products against ground based, airborne and other satellite based measurements. 3) The provision of an assessment of the quality of different IASI water vapour profile algorithms developed by the project partners and other groups. 4) The provision of a complete processing system that can further strengthen operational production of the developed products. 5) A demonstration of the use of the products in the field of climate modelling, including applying alternative ways of climate model validation using forward radiation operators. 6) The promotion of the strategy of data set construction and the data sets themselves to the global research and operational community. The ultimate goal of the

  15. Modeling brine and nutrient dynamics in Antarctic sea ice: The case of dissolved silica

    NASA Astrophysics Data System (ADS)

    Vancoppenolle, Martin; Goosse, Hugues; de Montety, Anne; Fichefet, Thierry; Tremblay, Bruno; Tison, Jean-Louis

    2010-02-01

    Sea ice ecosystems are characterized by microalgae living in brine inclusions. The growth rate of ice algae depends on light and nutrient supply. Here, the interactions between nutrients and brine dynamics under the influence of algae are investigated using a one-dimensional model. The model includes snow and ice thermodynamics with brine physics and an idealized sea ice biological component, characterized by one nutrient, namely, dissolved silica (DSi). In the model, DSi follows brine motion and is consumed by ice algae. Depending on physical ice characteristics, the brine flow is either advective, diffusive, or turbulent. The vertical profiles of ice salinity and DSi concentration are solutions of advection-diffusion equations. The model is configured to simulate the typical thermodynamic regimes of first-year Antarctic pack ice. The simulated vertical profiles of salinity and DSi qualitatively reproduce observations. Analysis of results highlights the role of convection in the lowermost 5-10 cm of ice. Convection mixes saline, nutrient-poor brine with comparatively fresh, nutrient-rich seawater. This implies a rejection of salt to the ocean and a flux of DSi to the ice. In the presence of growing algae, the simulated ocean-to-ice DSi flux increases by 0-115% compared to an abiotic situation. In turn, primary production and brine convection act in synergy to form a nutrient pump. The other important processes are the flooding of the surface by seawater and the percolation of meltwater. The former refills nutrients near the ice surface in spring. The latter, if present, tends to expell nutrients from the ice in summer.

  16. Calcium carbonate as ikaite crystals in Antarctic sea ice

    NASA Astrophysics Data System (ADS)

    Dieckmann, Gerhard S.; Nehrke, Gernot; Papadimitriou, Stathys; Göttlicher, Jörg; Steininger, Ralph; Kennedy, Hilary; Wolf-Gladrow, Dieter; Thomas, David N.

    2008-04-01

    We report on the discovery of the mineral ikaite (CaCO3.6H2O) in sea-ice from the Southern Ocean. The precipitation of CaCO3 during the freezing of seawater has previously been predicted from thermodynamic modelling, indirect measurements, and has been documented in artificial sea ice during laboratory experiments but has not been reported for natural sea-ice. It is assumed that CaCO3 formation in sea ice may be important for a sea ice-driven carbon pump in ice-covered oceanic waters. Without direct evidence of CaCO3 precipitation in sea ice, its role in this and other processes has remained speculative. The discovery of CaCO3.6H2O crystals in natural sea ice provides the necessary evidence for the evaluation of previous assumptions and lays the foundation for further studies to help elucidate the role of ikaite in the carbon cycle of the seasonally sea ice-covered regions

  17. Bacterial Communities of Surface Mixed Layer in the Pacific Sector of the Western Arctic Ocean during Sea-Ice Melting

    PubMed Central

    Ha, Ho Kyung; Kim, Hyun Cheol; Kim, Ok-Sun; Lee, Bang Yong; Cho, Jang-Cheon; Hur, Hor-Gil; Lee, Yoo Kyung

    2014-01-01

    From July to August 2010, the IBRV ARAON journeyed to the Pacific sector of the Arctic Ocean to monitor bacterial variation in Arctic summer surface-waters, and temperature, salinity, fluorescence, and nutrient concentrations were determined during the ice-melting season. Among the measured physicochemical parameters, we observed a strong negative correlation between temperature and salinity, and consequently hypothesized that the melting ice decreased water salinity. The bacterial community compositions of 15 samples, includicng seawater, sea-ice, and melting pond water, were determined using a pyrosequencing approach and were categorized into three habitats: (1) surface seawater, (2) ice core, and (3) melting pond. Analysis of these samples indicated the presence of local bacterial communities; a deduction that was further corroborated by the discovery of seawater- and ice-specific bacterial phylotypes. In all samples, the Alphaproteobacteria, Flavobacteria, and Gammaproteobacteria taxa composed the majority of the bacterial communities. Among these, Alphaproteobacteria was the most abundant and present in all samples, and its variation differed among the habitats studied. Linear regression analysis suggested that changes in salinity could affect the relative proportion of Alphaproteobacteria in the surface water. In addition, the species-sorting model was applied to evaluate the population dynamics and environmental heterogeneity in the bacterial communities of surface mixed layer in the Arctic Ocean during sea-ice melting. PMID:24497990

  18. Bacterial communities of surface mixed layer in the Pacific sector of the western Arctic Ocean during sea-ice melting.

    PubMed

    Han, Dukki; Kang, Ilnam; Ha, Ho Kyung; Kim, Hyun Cheol; Kim, Ok-Sun; Lee, Bang Yong; Cho, Jang-Cheon; Hur, Hor-Gil; Lee, Yoo Kyung

    2014-01-01

    From July to August 2010, the IBRV ARAON journeyed to the Pacific sector of the Arctic Ocean to monitor bacterial variation in Arctic summer surface-waters, and temperature, salinity, fluorescence, and nutrient concentrations were determined during the ice-melting season. Among the measured physicochemical parameters, we observed a strong negative correlation between temperature and salinity, and consequently hypothesized that the melting ice decreased water salinity. The bacterial community compositions of 15 samples, includicng seawater, sea-ice, and melting pond water, were determined using a pyrosequencing approach and were categorized into three habitats: (1) surface seawater, (2) ice core, and (3) melting pond. Analysis of these samples indicated the presence of local bacterial communities; a deduction that was further corroborated by the discovery of seawater- and ice-specific bacterial phylotypes. In all samples, the Alphaproteobacteria, Flavobacteria, and Gammaproteobacteria taxa composed the majority of the bacterial communities. Among these, Alphaproteobacteria was the most abundant and present in all samples, and its variation differed among the habitats studied. Linear regression analysis suggested that changes in salinity could affect the relative proportion of Alphaproteobacteria in the surface water. In addition, the species-sorting model was applied to evaluate the population dynamics and environmental heterogeneity in the bacterial communities of surface mixed layer in the Arctic Ocean during sea-ice melting.

  19. [Psycrophilic organisms in snow and ice].

    PubMed

    Kohshima, S

    2000-12-01

    Psychrophilic and psycrotrophic organisms are important in global ecology as a large proportion of our planet is cold. Two-third of sea-water covering more than 70% of Earth is cold deep sea water with temperature around 2 degrees C, and more than 90% of freshwater is in polar ice-sheets and mountain glaciers. Though biological activity in snow and ice had been believed to be extremely limited, various specialized biotic communities were recently discovered at glaciers of various part of the world. The glacier is relatively simple and closed ecosystem with special biotic community containing various psychrophilic and psycrotrophic organisms. Since psychrophilic organisms was discovered in the deep ice-core recovered from the antarctic ice-sheet and a lake beneath it, snow and ice environments in Mars and Europa are attracting a great deal of scientific attention as possible extraterrestrial habitats of life. This paper briefly reviews the results of the studies on ecology of psychrophilic organisms living in snow and ice environments and their physiological and biochemical adaptation to low temperature.

  20. Low salinity and high-level UV-B radiation reduce single-cell activity in antarctic sea ice bacteria.

    PubMed

    Martin, Andrew; Hall, Julie; Ryan, Ken

    2009-12-01

    Experiments simulating the sea ice cycle were conducted by exposing microbes from Antarctic fast ice to saline and irradiance regimens associated with the freeze-thaw process. In contrast to hypersaline conditions (ice formation), the simulated release of bacteria into hyposaline seawater combined with rapid exposure to increased UV-B radiation significantly reduced metabolic activity.

  1. Basal channels on ice shelves

    NASA Astrophysics Data System (ADS)

    Sergienko, O. V.

    2013-09-01

    Recent surveys of floating ice shelves associated with Pine Island Glacier (Antarctica) and Petermann Glacier (Greenland) indicate that there are channels incised upward into their bottoms that may serve as the conduits of meltwater outflow from the sub-ice-shelf cavity. The formation of the channels, their evolution over time, and their impact on ice-shelf flow are investigated using a fully-coupled ice-shelf/sub-ice-shelf ocean model. The model simulations suggest that channels may form spontaneously in response to meltwater plume flow initiated at the grounding line if there are relatively high melt rates and if there is transverse to ice-flow variability in ice-shelf thickness. Typical channels formed in the simulations have a width of about 1-3 km and a vertical relief of about 100-200 m. Melt rates and sea-water transport in the channels are significantly higher than on the smooth flat ice bottom between the channels. The melt channels develop through melting, deformation, and advection with ice-shelf flow. Simulations suggest that both steady state and cyclic state solutions are possible depending on conditions along the lateral ice-shelf boundaries. This peculiar dynamics of the system has strong implications on the interpretation of observations. The richness of channel morphology and evolution seen in this study suggests that further observations and theoretical analysis are imperative for understanding ice-shelf behavior in warm oceanic conditions.

  2. The Effects of Salt Water on Mechanical Properties of Glacial Ice

    NASA Astrophysics Data System (ADS)

    Holt, R. A.; McCarthy, C.

    2017-12-01

    An improved understanding of the mechanical properties of glacial ice, including factors that may change them, is essential for understanding vulnerability of ice sheets to climate change. It is understood that the temperature of intruding subglacial seawater affects the melting of glacial ice and therefore destabilizes ice shelves, but we hypothesize that seawater bathing the bottom of the glacier may also influence mechanical properties such as friction and elastic modulus. We undertook experiments to determine how the presence of saline solution at grain boundaries of ice might lead to weaker behavior. We created an ice sample by finely grinding and sieving seed ice, pressing it into a rectangular mold, and flooding with a 3.5wt% saline solution. We then quickly brought it to subsolidus (-22°) to completely freeze. The bulk composition of the sample was determined by refractive index to be 0.28wt%. Microstructural characterization of the sample indicates that, above the solidus, the melt phase was located at grain triple junctions and along grain boundaries. To test the frictional behavior of ice with saline sliding against rock, we used a cryo-biaxial apparatus designed to simulate the basal sliding of glacial ice. The experiments were run in the double direct configuration at 100 KPa normal stress and at T=-5°. The results demonstrate that ice containing a liquid saline solution has lower steady state friction than pure ice at the same conditions, and therefore can slip at a faster velocity. In addition to the bi-axial experiment we determined the elastic properties using an ultrasonic velocity testing system. P waves velocities through the saline ice sample were consistent with published values (Spencer et al., 1968, JGR). We also used both measured and estimated values to calculate the Young's modulus. We found that ice containing salt water has a lower Young's modulus than that of pure ice. Salt water significantly changes the mechanical properties of

  3. Formation of melt channels on ice shelves

    NASA Astrophysics Data System (ADS)

    Sergienko, Olga

    2013-04-01

    Melt channels have been observed on ice shelves experiencing strong melting in both Greenland (Petermann Glacier) and Antarctica (Pine Island Glacier). Using a fully-couple ice-shelf/sub-ice-shelf-ocean flow model, it is demonstrated that these channels can form spontaneously in laterally confined ice shelves. These channels have transverse extent of a few kilometers and a vertical relief of about a few hundred meters. Meltrates and sea-water transport in the channels are significantly higher than in between the channels on the smooth flat ice bottom. In circumstances where an ice shelf has no-slip conditions at its lateral boundaries, the ice-shelf/sub-ice-shelf-cavity system exhibits equilibrium periodic states, where the same configurations repetitively appear with a periodicity of about 30-35 years. This peculiar dynamics of the system has strong implications on the interpretation of the remote and in-situ observations and inferences of the system parameters (e.g., melt rates) based on these observations. For instance, the persistent temporal changes in the ice-shelf thickness are caused by internal dynamics of the melt channels, and, in contrast to traditional interpretation, can be independent of the oceanic forcings.

  4. Modeling brine and nutrient dynamics in Antarctic sea ice: the case of dissolved silica

    NASA Astrophysics Data System (ADS)

    Vancoppenolle, M.; Goosse, H.; de Montety, A.; Fichefet, T.; Tremblay, B.; Tison, J.

    2009-12-01

    Sea ice ecosystems are characterized by micro-algae living in brine inclusions. The growth rate of ice algae depends on light and nutrient supply. Here, the interactions between nutrients and brine dynamics under the influence of algae are investigated using a one-dimensional model. The model includes snow and ice thermodynamics with brine physics and an idealized sea ice biological component, characterized by one nutrient, namely dissolved silica (DSi). In the model, DSi follows brine motion and is consumed by ice algae. Depending on physical ice characteristics, the brine flow is either advective, diffusive or turbulent. The vertical profiles of ice salinity and DSi concentration are solutions of advection-diffusion equations. The model is configured to simulate the typical thermodynamic regimes of first-year Antarctic pack ice. The simulated vertical profiles of salinity and DSi qualitatively reproduce observations. Analysis of results highlights the role of convection in the lowermost 5-10 cm of ice. Convection mixes saline, nutrient-poor brine with comparatively fresh, nutrient-rich seawater. This implies a rejection of salt to the ocean and a flux of DSi to the ice. In presence of growing algae, the simulated ocean-to-ice DSi flux increases by 0-115% compared to an abiotic situation. In turn, primary production and brine convection act in synergy to form a nutrient pump. The other important processes are the flooding of the surface by seawater and the percolation of meltwater. The former refills nutrients near the ice surface in spring. The latter, if present, tends to expell nutrients from the ice in summer. Sketch of salt (left) and nutrient (right) exchanges at the ice-ocean interface proposed in this paper.

  5. Reliable determination of oxygen and hydrogen isotope ratios in atmospheric water vapour adsorbed on 3A molecular sieve.

    PubMed

    Han, Liang-Feng; Gröning, Manfred; Aggarwal, Pradeep; Helliker, Brent R

    2006-01-01

    The isotope ratio of atmospheric water vapour is determined by wide-ranging feedback effects from the isotope ratio of water in biological water pools, soil surface horizons, open water bodies and precipitation. Accurate determination of atmospheric water vapour isotope ratios is important for a broad range of research areas from leaf-scale to global-scale isotope studies. In spite of the importance of stable isotopic measurements of atmospheric water vapour, there is a paucity of published data available, largely because of the requirement for liquid nitrogen or dry ice for quantitative trapping of water vapour. We report results from a non-cryogenic method for quantitatively trapping atmospheric water vapour using 3A molecular sieve, although water is removed from the column using standard cryogenic methods. The molecular sieve column was conditioned with water of a known isotope ratio to 'set' the background signature of the molecular sieve. Two separate prototypes were developed, one for large collection volumes (3 mL) and one for small collection volumes (90 microL). Atmospheric water vapour was adsorbed to the column by pulling air through the column for several days to reach the desired final volume. Water was recovered from the column by baking at 250 degrees C in a dry helium or nitrogen air stream and cryogenically trapped. For the large-volume apparatus, the recovered water differed from water that was simultaneously trapped by liquid nitrogen (the experimental control) by 2.6 per thousand with a standard deviation (SD) of 1.5 per thousand for delta(2)H and by 0.3 per thousand with a SD of 0.2 per thousand for delta(18)O. Water-vapour recovery was not satisfactory for the small volume apparatus. Copyright (c) 2006 John Wiley & Sons, Ltd.

  6. Diversity and Vertical Distribution of Microbial Eukaryotes in the Snow, Sea Ice and Seawater Near the North Pole at the End of the Polar Night

    PubMed Central

    Bachy, Charles; López-García, Purificación; Vereshchaka, Alexander; Moreira, David

    2011-01-01

    Our knowledge about the microorganisms living in the high Arctic Ocean is still rudimentary compared to other oceans mostly because of logistical challenges imposed by its inhospitable climate and the presence of a multi-year ice cap. We have used 18S rRNA gene libraries to study the diversity of microbial eukaryotes in the upper part of the water column (0–170 m depth), the sea ice (0–1.5 m depth) and the overlying snow from samples collected in the vicinity of the North Pole (N88°35′, E015°59) at the very end of the long polar night. We detected very diverse eukaryotes belonging to Alveolata, Fungi, Amoebozoa, Viridiplantae, Metazoa, Rhizaria, Heterokonta, and Telonemia. Different alveolates (dinoflagellates and Marine Alveolate Groups I and II species) were the most abundant and diverse in gene libraries from water and sea ice, representing 80% of the total number of clones and operational taxonomic units. Only contaminants and/or species from continental ecosystems were detected in snow, suggesting wind- and animal- or human-mediated cosmopolitan dispersal of some taxa. By contrast, sea ice and seawater samples harbored a larger and more similar inter-sample protist diversity as compared with snow. The North Pole was found to harbor distinctive eukaryotic communities along the vertical gradient with an unparalleled diversity of core dinoflagellates, largely dominant in libraries from the water column, as compared to other oceanic locations. In contrast, phototrophic organisms typical of Arctic sea ice and plankton, such as diatoms and prasinophytes, were very rare in our samples. This was most likely due to a decrease of their populations after several months of polar night darkness and to the presence of rich populations of diverse grazers. Whereas strict phototrophs were scarce, we identified a variety of likely mixotrophic taxa, which supports the idea that mixotrophy may be important for the survival of diverse protists through the long polar

  7. Fuel Production from Seawater and Fuel Cells Using Seawater.

    PubMed

    Fukuzumi, Shunichi; Lee, Yong-Min; Nam, Wonwoo

    2017-11-23

    Seawater is the most abundant resource on our planet and fuel production from seawater has the notable advantage that it would not compete with growing demands for pure water. This Review focuses on the production of fuels from seawater and their direct use in fuel cells. Electrolysis of seawater under appropriate conditions affords hydrogen and dioxygen with 100 % faradaic efficiency without oxidation of chloride. Photoelectrocatalytic production of hydrogen from seawater provides a promising way to produce hydrogen with low cost and high efficiency. Microbial solar cells (MSCs) that use biofilms produced in seawater can generate electricity from sunlight without additional fuel because the products of photosynthesis can be utilized as electrode reactants, whereas the electrode products can be utilized as photosynthetic reactants. Another important source for hydrogen is hydrogen sulfide, which is abundantly found in Black Sea deep water. Hydrogen produced by electrolysis of Black Sea deep water can also be used in hydrogen fuel cells. Production of a fuel and its direct use in a fuel cell has been made possible for the first time by a combination of photocatalytic production of hydrogen peroxide from seawater and dioxygen in the air and its direct use in one-compartment hydrogen peroxide fuel cells to obtain electric power. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  8. Influence of Sea Ice Crack Formation on the Spatial Distribution of Nutrients and Microalgae in Flooded Antarctic Multiyear Ice

    NASA Astrophysics Data System (ADS)

    Nomura, Daiki; Aoki, Shigeru; Simizu, Daisuke; Iida, Takahiro

    2018-02-01

    Cracks are common and natural features of sea ice formed in the polar oceans. In this study, a sea ice crack in flooded, multiyear, land-fast Antarctic sea ice was examined to assess its influence on biological productivity and the transport of nutrients and microalgae into the upper layers of neighboring sea ice. The water inside the crack and the surrounding host ice were characterized by a strong discoloration (brown color), an indicator of a massive algal bloom. Salinity and oxygen isotopic ratio measurements indicated that 64-84% of the crack water consisted of snow meltwater supplied during the melt season. Measurements of nutrient and chlorophyll a concentrations within the slush layer pool (the flooded layer at the snow-ice interface) revealed the intrusion of water from the crack, likely forced by mixing with underlying seawater during the tidal cycle. Our results suggest that sea ice crack formation provides conditions favorable for algal blooms by directly exposing the crack water to sunlight and supplying nutrients from the under-ice water. Subsequently, constituents of the crack water modified by biological activity were transported into the upper layer of the flooded sea ice. They were then preserved in the multiyear ice column formed by upward growth of sea ice caused by snow ice formation in areas of significant snow accumulation.

  9. Ocean interactions with the base of Amery Ice Shelf, Antarctica

    NASA Technical Reports Server (NTRS)

    Hellmer, Hartmut H.; Jacobs, Stanley S.

    1992-01-01

    Using a two-dimensional ocean themohaline circulation model, we varied the cavity shape beneath Amery Ice Shelf in an attempt to reproduce the 150-m-thick marine ice layer observed at the 'G1' ice core site. Most simulations caused melting rates which decrease the ice thickness by as much as 400 m between grounding line and G1, but produce only minor accumulation at the ice core site and closer to the ice front. Changes in the sea floor and ice topographies revealed a high sensitivity of the basal mass balance to water column thickness near the grounding line, to submarine sills, and to discontinuities in ice thickness. Model results showed temperature/salinity gradients similar to observations from beneath other ice shelves where ice is melting into seawater. Modeled outflow characteristics at the ice front are in general agreement with oceanographic data from Prydz Bay. We concur with Morgan's inference that the G1 core may have been taken in a basal crevasse filled with marine ice. This ice is formed from water cooled by ocean/ice shelf interactions along the interior ice shelf base.

  10. Understanding Spatial and Temporal Variations of Arctic Circulation Using Oxygen Isotopes of Seawater

    NASA Astrophysics Data System (ADS)

    Yin, L.; Kopans-Johnson, C. R.; LeGrande, A. N.; Kelly, S.

    2015-12-01

    The isotopic ratio of 18O to 16O in seawater (2005ppm in ocean water is defined as 𝛿18Oseawater≡0 permil or 0‰) is a fundamental ocean tracer due to its distinct linear relationship with salinity(𝛿18O -S) from regional inland freshwater sources. As opposed to salinity alone, 𝛿18O distinguishes river runoff from sea-ice melt and traces ocean circulation pathways from coastal to open waters and surface to deep waters. Observations from the past 60 years of 𝛿18O seawater were compiled into a database by Schimdt et al. (1999), and subsequently used to calculate a 3-dimensional 1°x1° 𝛿18O global gridded dataset by LeGrande and Schmidt (2006). Although the Schmidt et al. (1999) Global Seawater Oxygen-18 Database (𝛿18Oobs) contains 25,514 measurements used to calculate the global gridded dataset, LeGrande and Schmidt (2006) point out that, "data coverage varies greatly from region to region," with seasonal variability creating biases in areas where sea ice is present. Python Pandas is used to automate the addition of 2,942 records to the Schmidt et al. (1999) Global Seawater Oxygen-18 Database (𝛿18Oobs), and examine the spatial and temporal distributions of 18O in the Arctic Ocean. 10 initial water masses are defined using spatial and temporal trends, clusters of observations, and Arctic surface circulation. Jackknife slope analysis of water mass 𝛿18O -S is used to determine anomalous data points and regional hydrology, resulting in 4 distinct Arctic water masses. These techniques are used to improve the gridded 𝛿18Oseawater dataset by distinguishing unique water masses, and accounting for seasonal variability of complex high latitude areas.

  11. Seawater 234U/238U recorded by modern and fossil corals

    NASA Astrophysics Data System (ADS)

    Chutcharavan, Peter M.; Dutton, Andrea; Ellwood, Michael J.

    2018-03-01

    U-series dating of corals is a crucial tool for generating absolute chronologies of Late Quaternary sea-level change and calibrating the radiocarbon timescale. Unfortunately, coralline aragonite is susceptible to post-depositional alteration of its primary geochemistry. One screening technique used to identify unaltered corals relies on the back-calculation of initial 234U/238U activity (δ234Ui) at the time of coral growth and implicitly assumes that seawater δ234U has remained constant during the Late Quaternary. Here, we test this assumption using the most comprehensive compilation to date of coral U-series measurements. Unlike previous compilations, this study normalizes U-series measurements to the same decay constants and corrects for offsets in interlaboratory calibrations, thus reducing systematic biases between reported δ234U values. Using this approach, we reassess (a) the value of modern seawater δ234U, and (b) the evolution of seawater δ234U over the last deglaciation. Modern coral δ234U values (145.0 ± 1.5‰) agree with previous measurements of seawater and modern corals only once the data have been normalized. Additionally, fossil corals in the surface ocean display δ234Ui values that are ∼5-7‰ lower during the last glacial maximum regardless of site, taxon, or diagenetic setting. We conclude that physical weathering of U-bearing minerals exposed during ice sheet retreat drives the increase in δ234U observed in the oceans, a mechanism that is consistent with the interpretation of the seawater Pb-isotope signal over the same timescale.

  12. Formation and character of an ancient 19-m ice cover and underlying trapped brine in an "ice-sealed" east Antarctic lake.

    PubMed

    Doran, Peter T; Fritsen, Christian H; McKay, Christopher P; Priscu, John C; Adams, Edward E

    2003-01-07

    Lake Vida, one of the largest lakes in the McMurdo Dry Valleys of Antarctica, was previously believed to be shallow (<10 m) and frozen to its bed year-round. New ice-core analysis and temperature data show that beneath 19 m of ice is a water column composed of a NaCl brine with a salinity seven times that of seawater that remains liquid below -10 degrees C. The ice cover thickens at both its base and surface, sealing concentrated brine beneath. The ice cover is stabilized by a negative feedback between ice growth and the freezing-point depression of the brine. The ice cover contains frozen microbial mats throughout that are viable after thawing and has a history that extends to at least 2,800 (14)C years B.P., suggesting that the brine has been isolated from the atmosphere for as long. To our knowledge, Lake Vida has the thickest subaerial lake ice cover recorded and may represent a previously undiscovered end-member lacustrine ecosystem on Earth.

  13. Convective Troposphere-Stratosphere Transport in the Tropics and Hydration by ice Crystals Geysers

    NASA Astrophysics Data System (ADS)

    Pommereau, J.

    2008-12-01

    Twenty-five years ago the suggestion was made by Danielsen of direct fast convective penetration of tropospheric air in the stratosphere over land convective systems. Although the existence of the mechanism is accepted, it was thought to be rare and thus its contribution to Troposphere-Stratosphere Transport (TST) of chemical species and water vapour at global scale unimportant at global scale. In contrast to this assumption, observations of temperature, water vapour, ice particles, long-lived tropospheric species during HIBISCUS, TROCCINOX and SCOUT-O3 over Brazil, Australia and Africa and more recently CALIPSO aerosols observations suggest that it is a general feature of tropical land convective regions in the summer. Particularly relevant to stratospheric water vapour is the observation of geyser like ice crystals in the TTL over overshooting events which may result in the moistening of the stratosphere. Although such events successfully captured by small scale Cloud-Resolving Models may have a significant impact on stratospheric ozone chemistry and climate, they are currently totally ignored by NWPs, CTMs and CCMs. Several recent balloon and aircraft observations of overshoots and CRM simulations will be shown illustrating the mechanism, as well as observations from a variety of satellites suggesting a significant impact at global scale.

  14. Resuspended dust as a novel source of marine ice nucleating particles

    NASA Astrophysics Data System (ADS)

    Cornwell, G.; Sultana, C. M.; Schill, G. P.; Hill, T. C. J.; Cochran, R. E.; DeMott, P. J.; Prather, K. A.

    2017-12-01

    Recent studies of marine ice nucleating particles (INPs) have focused upon their production from phytoplankton blooms, the products of their metabolism, and resulting from their decomposition. In this work, we provide evidence for an additional, inorganic source of marine INPs independent of the marine mesocosm. Laboratory studies of aerosols generated from both synthetic seawater solutions spiked with mineral dust and from nascent coastal Pacific Ocean seawater indicate that dust can be ejected from seawater during the bubble bursting processes. Online and offline measurements of INP concentrations showed that these dust particles were ice nucleation-active in concentrations up to 40 L-1 at -30 °C, an order of magnitude more than those found in marine boundary layers or in laboratory mesocosms. Additional single particle composition measurements using an aerosol time of flight mass spectrometer (ATOFMS) collected along the Californian coast at Bodega Marine Laboratory found dust particles that contained markers from internal mixing with sea salt similar to those observed in the laboratory studies. The evidence from both laboratory and field studies suggests that there is a reservoir of dust particles within the ocean that can be ejected from the ocean's surface and act as INPs.

  15. Hydrocarbon biodegradation by Arctic sea-ice and sub-ice microbial communities during microcosm experiments, Northwest Passage (Nunavut, Canada).

    PubMed

    Garneau, Marie-Ève; Michel, Christine; Meisterhans, Guillaume; Fortin, Nathalie; King, Thomas L; Greer, Charles W; Lee, Kenneth

    2016-10-01

    The increasing accessibility to navigation and offshore oil exploration brings risks of hydrocarbon releases in Arctic waters. Bioremediation of hydrocarbons is a promising mitigation strategy but challenges remain, particularly due to low microbial metabolic rates in cold, ice-covered seas. Hydrocarbon degradation potential of ice-associated microbes collected from the Northwest Passage was investigated. Microcosm incubations were run for 15 days at -1.7°C with and without oil to determine the effects of hydrocarbon exposure on microbial abundance, diversity and activity, and to estimate component-specific hydrocarbon loss. Diversity was assessed with automated ribosomal intergenic spacer analysis and Ion Torrent 16S rRNA gene sequencing. Bacterial activity was measured by (3)H-leucine uptake rates. After incubation, sub-ice and sea-ice communities degraded 94% and 48% of the initial hydrocarbons, respectively. Hydrocarbon exposure changed the composition of sea-ice and sub-ice communities; in sea-ice microcosms, Bacteroidetes (mainly Polaribacter) dominated whereas in sub-ice microcosms, the contribution of Epsilonproteobacteria increased, and that of Alphaproteobacteria and Bacteroidetes decreased. Sequencing data revealed a decline in diversity and increases in Colwellia and Moritella in oil-treated microcosms. Low concentration of dissolved organic matter (DOM) in sub-ice seawater may explain higher hydrocarbon degradation when compared to sea ice, where DOM was abundant and composed of labile exopolysaccharides. © Fisheries and Oceans Canada [2016].

  16. Mechanisms and implications of α-HCH enrichment in melt pond water on Arctic sea ice.

    PubMed

    Pućko, M; Stern, G A; Barber, D G; Macdonald, R W; Warner, K-A; Fuchs, C

    2012-11-06

    During the summer of 2009, we sampled 14 partially refrozen melt ponds and the top 1 m of old ice in the pond vicinity for α-hexachlorocyclohexane (α-HCH) concentrations and enantiomer fractions (EFs) in the Beaufort Sea. α-HCH concentrations were 3 - 9 times higher in melt ponds than in the old ice. We identify two routes of α-HCH enrichment in the ice over the summer. First, atmospheric gas deposition results in an increase of α-HCH concentration from 0.07 ± 0.02 ng/L (old ice) to 0.34 ± 0.08 ng/L, or ~20% less than the atmosphere-water equilibrium partitioning concentration (0.43 ng/L). Second, late-season ice permeability and/or complete ice thawing at the bottom of ponds permit α-HCH rich seawater (~0.88 ng/L) to replenish pond water, bringing concentrations up to 0.75 ± 0.06 ng/L. α-HCH pond enrichment may lead to substantial concentration patchiness in old ice floes, and changed exposures to biota as the surface meltwater eventually reaches the ocean through various drainage mechanisms. Melt pond concentrations of α-HCH were relatively high prior to the late 1980-s, with a Melt pond Enrichment Factor >1 (MEF; a ratio of concentration in surface meltwater to surface seawater), providing for the potential of increased biological exposures.

  17. On the GIBBS thermodynamic potential of seawater

    NASA Astrophysics Data System (ADS)

    Feistel, Rainer; Hagen, Eberhard

    Free Enthalpy, the GIBBS thermodynamic potential G(S,t,p) of seawater, has been recomputed including the sound speed equation of DEL GROSSO (1974), temperatures of maximum density (TMD) of CALDWELL (1978), freezing point depression measurements of DOHERTY and KESTER (1974), rederived limiting laws and ice properties, and an extended set of dilution heat data of BROMLEY (1968) and MILLERO, HANSEN and HOFF (1973). As a new reference state, the standard ocean state has been chosen. The resulting average deviations are 0.0006 kg m -3 for pure water density at 1 atm, 0.002 kg m -3 for seawater density at 1 atm, 0.02 m/s for sound speed, 0.01 J kgK -1 for heat capacity at 1 atm, 0.4 kJ kg -1 for dilution heats, 0.002°C for freezing points, and 0.04°C for TMDs. Resulting pressure-dependent freezing points are in good agreement with experiments and UNESCO (1978) formulas. Enthalpy as thermodynamic potential has been explicitly determined for easy computation of potential temperature, potential density, and sound speed. All functions are expressed in the new International Temperature Scale ITS-90.

  18. Moisture rainout fraction over the Indian Ocean during austral summer based on (18) {O}/{}(16) {O}18O/16O ratios of surface seawater, rainwater at latitude range of 10({°) } {N}textendash 60({°) } {S}10∘N–60∘S

    NASA Astrophysics Data System (ADS)

    Prasanna, K.; Ghosh, Prosenjit; Bhattacharya, S. K.; Rahul, P.; Yoshimura, Kei; Anilkumar, N.

    2018-06-01

    Oxygen isotope ratios (^{18}O/^{16}O) of surface seawater and rainwater samples from the Indian Ocean region (10°Nendash 60°S) during austral summer collected onboard ORV Sagar Nidhi during 2011-2013 have been measured along with salinity, sea surface temperature and relative humidity. The rainwater is isotopically lighter (by 4.6± 2.7\\permille ) compared to the equilibrium condensation of the vapour arising from the seawater at the ambient condition. The isotopic composition of the vapour at high altitude responsible for the rain formation at the sampling location is estimated from a global atmospheric water isotope model (IsoGSM2). The apparent deficit of ˜ 5\\permille can be explained by invoking a high degree of rainout (on average, about 70% of the overhead atmospheric moisture) during transport of the source vapour to the sampling location undergoing a Rayleigh fractionation. The required rainout fraction is higher (˜ 80%) in the latitude belt 40°endash 60°S compared to the equatorial belt (˜ 60%). The pattern of variation in the rainout fraction with latitude is consistent with the well-known evaporation/precipitation processes in the Indian Ocean.

  19. Vapour Intrusion into Buildings - A Literature Review

    EPA Science Inventory

    This chapter provides a review of recent research on vapour intrusion of volatile organic compounds (VOCs) into buildings. The chapter builds on a report from Tillman and Weaver (2005) which reviewed the literature on vapour intrusion through 2005. Firstly, the term ‘vapour intru...

  20. Formation and character of an ancient 19-m ice cover and underlying trapped brine in an “ice-sealed” east Antarctic lake

    PubMed Central

    Doran, Peter T.; Fritsen, Christian H.; McKay, Christopher P.; Priscu, John C.; Adams, Edward E.

    2003-01-01

    Lake Vida, one of the largest lakes in the McMurdo Dry Valleys of Antarctica, was previously believed to be shallow (<10 m) and frozen to its bed year-round. New ice-core analysis and temperature data show that beneath 19 m of ice is a water column composed of a NaCl brine with a salinity seven times that of seawater that remains liquid below −10°C. The ice cover thickens at both its base and surface, sealing concentrated brine beneath. The ice cover is stabilized by a negative feedback between ice growth and the freezing-point depression of the brine. The ice cover contains frozen microbial mats throughout that are viable after thawing and has a history that extends to at least 2,800 14C years B.P., suggesting that the brine has been isolated from the atmosphere for as long. To our knowledge, Lake Vida has the thickest subaerial lake ice cover recorded and may represent a previously undiscovered end-member lacustrine ecosystem on Earth. PMID:12518052

  1. A comparison of the static and flow methods for the detection of ice nuclei

    NASA Astrophysics Data System (ADS)

    Hussain, K.; Kayani, S. A.

    The use of the membrane-filter processing chamber to study ice nuclei concentrations has become wide-spread since its introduction by Bigg et al. in 1961. The technique is convenient because of the simplicity of its operation and because it could be run remote from the place of field study. It has however been found to suffer from a number of drawbacks, namely, the volume effect, the chamber height effect, the vapour depletion effect, etc. Comparison of the results obtained by running a traditional filter processor and a continuous flow chamber under identical temperature and humidity conditions for polluted Manchester air has shown that the latter technique detects more ice nuclei than the former one by a factor of about 14±4. These results confirm that the filter technique suffers from the vapour depletion effect. The present results are in agreement with Bigg et al., Mossop and Thorndike, and King. In the light of our findings the filter technique does not appear to be a standard method. Therefore the ice nuclei data obtained with the filter method should not be extended to clouds in order to study their microphysical properties.

  2. Localized sources of water vapour on the dwarf planet (1) Ceres.

    PubMed

    Küppers, Michael; O'Rourke, Laurence; Bockelée-Morvan, Dominique; Zakharov, Vladimir; Lee, Seungwon; von Allmen, Paul; Carry, Benoît; Teyssier, David; Marston, Anthony; Müller, Thomas; Crovisier, Jacques; Barucci, M Antonietta; Moreno, Raphael

    2014-01-23

    The 'snowline' conventionally divides Solar System objects into dry bodies, ranging out to the main asteroid belt, and icy bodies beyond the belt. Models suggest that some of the icy bodies may have migrated into the asteroid belt. Recent observations indicate the presence of water ice on the surface of some asteroids, with sublimation a potential reason for the dust activity observed on others. Hydrated minerals have been found on the surface of the largest object in the asteroid belt, the dwarf planet (1) Ceres, which is thought to be differentiated into a silicate core with an icy mantle. The presence of water vapour around Ceres was suggested by a marginal detection of the photodissociation product of water, hydroxyl (ref. 12), but could not be confirmed by later, more sensitive observations. Here we report the detection of water vapour around Ceres, with at least 10(26) molecules being produced per second, originating from localized sources that seem to be linked to mid-latitude regions on the surface. The water evaporation could be due to comet-like sublimation or to cryo-volcanism, in which volcanoes erupt volatiles such as water instead of molten rocks.

  3. Studies of copper and gold vapour lasers

    NASA Astrophysics Data System (ADS)

    Clark, Graeme Lawrence

    The work described in this thesis covers various aspects of pulsed copper and gold vapour lasers. The work is divided into four main parts : a computer model of the kinetics of the copper vapour laser discharge; construction and characterization of a copper vapour laser and a gold vapour laser system (to be used for photodynamic cancer treatment); analysis of the thermal processes occurring in the various forms of thermal insulation used in these lasers; and studies of the use of metal walls to confine a discharge plasma. The results of this work were combined in the design of the first copper vapour laser to use metal rather than an electrically insulating ceramic material for confinement of the discharge plasma. Laser action in copper vapour has been achieved in a number of metal-walled designs, with continuous lengths of metal ranging from 30 mm, in a segmented design, to 400 mm, where the discharge plasma was confined by two molybdenum tubes of this length. A theoretical explanation of the behaviour of plasmas in metal-walled discharge vessels is described.

  4. "Crystals within Crystals: The Story of Sea Ice". A Classroom-Based Outreach Project Communicating Cutting-Edge Ocean Science to School Pupils

    NASA Astrophysics Data System (ADS)

    Butler, B.

    2016-02-01

    'Crystals within Crystals: The story of sea ice' is a UK based outreach project based that uses a range practical tools to engage school students with cutting edge scientific research that relates to the use of some of the world's most powerful X-rays in sea ice research. The project is delivered in the form of a classroom workshop that first introduces school pupils (aged 11-14) to seawater and the salts that give it a salinity. The pupils are then shown how the presence of salts within seawater results in very important physical changes when the liquid freezes, which includes different structural and optical properties of the ice. The properties of the ice are then linked to the presence of countless microscopic salt crystals that are trapped within the microstructure of the frozen seawater, which is explained with use of a novel crystal growth demonstration. Given that there is currently no way of successfully removing these salt crystals from the ice, the workshop culminates in explaining how some of the worlds most powerful X-rays can be used to investigate processes that otherwise remain elusive. The workshop introduces students to the fundamental principles of scientific enquiry, the sea ice environment, and the power of X-rays in investigating the properties of crystals. Here we present information that outlines a host of practical and project management tools that are applicacble to outreach projects in the the field of ocean sciences, with the aim of seeding ideas and interest for other graduate student to enage with the public during their studies.

  5. Do Europa's Mountains Have Roots? Erosion of Topography at the Ice-Water Interface via the "Ice Pump"

    NASA Astrophysics Data System (ADS)

    Goodman, J. C.

    2016-12-01

    Are topographic features on the surface of Europa and other icy worlds isostatically compensated by variations in shell thickness (Airy isostasy)? This is only possible if variations in shell thickness can remain stable over geologic time. Here we show that melting and freezing driven by the pressure dependence of the melting point of water - the "ice pump" - can rapidly erase topography at the ice/water interface. We consider ice pumps driven by both tidal action and buoyancy-driven flow. We first show that as tidal action drives the ocean up and down along a sloping interface, ice will be melted from areas where it's thickest and deposited where the ice is thinnest. We show that this process causes the ice interface topography to relax according to a simple "diffusion" linear partial differential equation. We estimate that a 10-km-wide topographic feature would be erased by the tidal ice pump in 3000 years if Europa's tidal current amplitude is 1 cm/s; however, this timescale is inversely proportional to the cube of the tidal velocity! Next, we consider an ice pump powered by ascent of meltwater along a sloping ice-water interface. We consider layer-averaged budgets for heat, mass, and momentum, along with turbulent mixing of the meltwater layer with underlying seawater via a Richardson number dependent entrainment process, and use these to estimate the thickness and mass flux of the meltwater layer. From this we estimate the rate of melting and freezing at the interface. These two ice pump processes combine with the glacial flow of warm basal ice to rapidly flatten out any variations in the height of the ice-water interface: Europa's ice/water interface may be perfectly flat! If so, topography at Europa's surface can only be supported by variations in density of the shell or the strength of the brittle surface ice.

  6. The impact of organic vapours on warm cloud formation; characterisation of chamber setup and first experimental results

    NASA Astrophysics Data System (ADS)

    Frey, Wiebke; Connolly, Paul; Dorsey, James; Hu, Dawei; Alfarra, Rami; McFiggans, Gordon

    2016-04-01

    The Manchester Ice Cloud Chamber (MICC), consisting of a 10m high stainless steel tube and 1m in diameter, can be used to study cloud processes. MICC is housed in three separate cold rooms stacked on top of each other and warm pseudo-adiabatic expansion from controlled initial temperature and pressure is possible through chamber evacuation. Further details about the facility can be found at http://www.cas.manchester.ac.uk/restools/cloudchamber/index.html. MICC can be connected to the Manchester Aerosol Chamber (MAC, http://www.cas.manchester.ac.uk/restools/aerosolchamber/), which allows to inject specified aerosol particles into the cloud chamber for nucleation studies. The combination of MAC and MICC will be used in the CCN-Vol project, which seeks to bring the experimental evidence for co-condensation of organic and water vapour in cloud formation which leads to an increase in cloud particle numbers (see Topping et al., 2013, Nature Geoscience Letters, for details). Here, we will show a characterisation of the cloud and aerosol chamber coupling in regard to background aerosol particles and nucleation. Furthermore, we will show preliminary results from the warm CCN-Vol experiment, investigating the impact of co-condensation of organic vapours and water vapour on warm cloud droplet formation.

  7. Bromoalkane production by Antarctic ice algae

    NASA Technical Reports Server (NTRS)

    Sturges, W. T.; Sullivan, C. W.; Schnell, R. C.; Heidt, L. E.; Pollock, W. H.

    1993-01-01

    Ice microalgae, collected from the underside of annual sea ice in McMurdo Sound, Antarctica, were found to contain and release to seawater a number of brominated hydrocarbons. These included bromoform, dibromomethane, mixed bromochloromethanes, and methyl bromide. Atmospheric measurements in the McMurdo Sound vicinity revealed the presence of bromoform and methyl bromide in the lower atmosphere, with lowest concentrations inland, further indicating that biogenic activity in the Sound is a source of organic bromine gases to the Antarctic atmosphere. This may have important implications for boundary layer chemistry in Antarctica. In the Arctic, the presence of bromoform has been linked to loss of surface ozone in the spring. We report here preliminary evidence for similar surface ozone loss at McMurdo Station.

  8. Frost flowers on young Arctic sea ice: The climatic, chemical, and microbial significance of an emerging ice type

    NASA Astrophysics Data System (ADS)

    Barber, D. G.; Ehn, J. K.; Pućko, M.; Rysgaard, S.; Deming, J. W.; Bowman, J. S.; Papakyriakou, T.; Galley, R. J.; Søgaard, D. H.

    2014-10-01

    Ongoing changes in Arctic sea ice are increasing the spatial and temporal range of young sea ice types over which frost flowers can occur, yet the significance of frost flowers to ocean-sea ice-atmosphere exchange processes remains poorly understood. Frost flowers form when moisture from seawater becomes available to a cold atmosphere and surface winds are low, allowing for supersaturation of the near-surface boundary layer. Ice grown in a pond cut in young ice at the mouth of Young Sound, NE Greenland, in March 2012, showed that expanding frost flower clusters began forming as soon as the ice formed. The new ice and frost flowers dramatically changed the radiative and thermal environment. The frost flowers were about 5°C colder than the brine surface, with an approximately linear temperature gradient from their base to their upper tips. Salinity and δ18O values indicated that frost flowers primarily originated from the surface brine skim. Ikaite crystals were observed to form within an hour in both frost flowers and the thin pond ice. Average ikaite concentrations were 1013 µmol kg-1 in frost flowers and 1061 µmol kg-1 in the surface slush layer. Chamber flux measurements confirmed an efflux of CO2 at the brine-wetted sea ice surface, in line with expectations from the brine chemistry. Bacteria concentrations generally increased with salinity in frost flowers and the surface slush layer. Bacterial densities and taxa indicated that a selective process occurred at the ice surface and confirmed the general pattern of primary oceanic origin versus negligible atmospheric deposition.

  9. Nature/culture/seawater.

    PubMed

    Helmreich, Stefan

    2011-01-01

    Seawater has occupied an ambiguous place in anthropological categories of "nature" and "culture." Seawater as nature appears as potentiality of form and uncontainable flux; it moves faster than culture - with culture frequently figured through land-based metaphors - even as culture seeks to channel water's (nature's) flow. Seawater as culture manifests as a medium of pleasure, sustenance, travel, disaster. I argue that, although seawater's qualities in early anthropology were portrayed impressionistically, today technical, scientific descriptions of water's form prevail. For example, processes of globalization - which may also be called "oceanization" - are often described as "currents," "flows," and "circulations." Examining sea-set ethnography, maritime anthropologies, and contemporary social theory, I propose that seawater has operated as a “theory machine” for generating insights about human cultural organization. I develop this argument with ethnography from the Sargasso Sea and in the Sea Islands. I conclude with a critique of appeals to water's form in social theory.

  10. Ice formation in altocumulus clouds over Leipzig: Remote sensing measurements and detailed model simulations

    NASA Astrophysics Data System (ADS)

    Simmel, Martin; Bühl, Johannes; Ansmann, Albert; Tegen, Ina

    2014-05-01

    Over Leipzig, altocumulus clouds are frequently observed using a suite of remote sensing instruments. These observations cover a wide range of heights, temperatures, and microphysical properties of the clouds ranging from purely liquid to heavily frozen. For the current study, two cases were chosen to test the sensitivity of these clouds with respect to several microphysical and dynamical parameters such as aerosol properties (CCN, IN), ice particle shape as well as turbulence. The mixed-phase spectral microphysical model SPECS was coupled to a dynamical model of the Asai-Kasahara type resulting in the model system AK-SPECS. The relatively simple dynamics allows for a fine vertical resolution needed for the rather shallow cloud layers observed. Additionally, the proper description of hydrometeor sedimentation is important especially for the fast growing ice crystals to realistically capture their interaction with the vapour and liquid phase (Bergeron-Findeisen process). Since the focus is on the cloud microphysics, the dynamics in terms of vertical velocity profile is prescribed for the model runs and the feedback of the microphysics on dynamics by release or consumption of latent heat due to phase transfer is not taken into account. The microphysics focuses on (1) ice particle shape allowing hexagonal plates and columns with size-dependant axis ratios and (2) the ice nuclei (IN) budget realized with a prognostic temperature resolved field of potential IN allowing immersion freezing only when active IN and supercooled drops above a certain size threshold are present within a grid cell. Sensitivity studies show for both cases that ice particle shape seems to have the major influence on ice mass formation under otherwise identical conditions. This is due to the effect (1) on terminal fall velocity of the individual ice particle allowing for longer presence times in conditions supersaturated with respect to ice and (2) on water vapour deposition which is enhanced due

  11. Numerical model of ice melange expansion during abrupt ice-shelf collapse

    NASA Astrophysics Data System (ADS)

    Guttenberg, N.; Abbot, D. S.; Amundson, J. M.; Burton, J. C.; Cathles, L. M.; Macayeal, D. R.; Zhang, W.

    2010-12-01

    Satellite imagery of the February 2008 Wilkins Ice-Shelf Collapse event reveals that a large percentage of the involved ice shelf was converted to capsized icebergs and broken fragments of icebergs over a relatively short period of time, possibly less than 24 hours. The extreme violence and short time scale of the event, and the considerable reduction of gravitational potential energy between upright and capsized icebergs, suggests that iceberg capsize might be an important driving mechanism controlling both the rate and spatial extent of ice shelf collapse. To investigate this suggestion, we have constructed an idealized, 2-dimensional model of a disintegrating ice shelf composed of a large number (N~100 to >1000) of initially well-packed icebergs of rectangular cross section. The model geometry consists of a longitudinal cross section of the idealized ice shelf from grounding line (or the upstream extent of ice-shelf fragmentation) to seaward ice front, and includes the region beyond the initial ice front to cover the open, ice-free water into which the collapsing ice shelf expands. The seawater in which the icebergs float is treated as a hydrostatic fluid in the computation of iceberg orientation (e.g., the evaluation of buoyancy forces and torques), thereby eliminating the complexities of free-surface waves, but net horizontal drift of the icebergs is resisted by a linear drag law designed to energy dissipation by viscous forces and surface-gravity-wave radiation. Icebergs interact via both elastic and inelastic contacts (typically a corner of one iceberg will scrape along the face of its neighbor). Ice-shelf collapse in the model is embodied by the mass capsize of a large proportion of the initially packed icebergs and the consequent advancement of the ice front (leading edge). Model simulations are conducted to examine (a) the threshold of stability (e.g., what density of initially capsizable icebergs is needed to allow a small perturbation to the system

  12. Impacts of seawater rise on seawater intrusion in the Nile Delta Aquifer, Egypt.

    PubMed

    Sefelnasr, Ahmed; Sherif, Mohsen

    2014-01-01

    Several investigations have recently considered the possible impacts of climate change and seawater level rise on seawater intrusion in coastal aquifers. All have revealed the severity of the problem and the significance of the landward movement of the dispersion zone under the condition of seawater level rise. Most of the studies did not consider the possible effects of the seawater rise on the inland movement of the shoreline and the associate changes in the boundary conditions at the seaside and the domain geometry. Such effects become more evident in flat, low land, coastal alluvial plans where large areas might be submerged with seawater under a relatively small increase in the seawater level. None of the studies combined the effect of increased groundwater pumping, due to the possible decline in precipitation and shortage in surface water resources, with the expected landward shift of the shore line. In this article, the possible effects of seawater level rise in the Mediterranean Sea on the seawater intrusion problem in the Nile Delta Aquifer are investigated using FEFLOW. The simulations are conducted in horizontal view while considering the effect of the shoreline landward shift using digital elevation models. In addition to the basic run (current conditions), six different scenarios are considered. Scenarios one, two, and three assume a 0.5 m seawater rise while the total pumping is reduced by 50%, maintained as per the current conditions and doubled, respectively. Scenarios four, five, and six assume a 1.0 m seawater rise and the total pumping is changed as in the first three scenarios. The shoreline is moved to account for the seawater rise and hence the study domain and the seaside boundary are modified accordingly. It is concluded that, large areas in the coastal zone of the Nile Delta will be submerged by seawater and the coast line will shift landward by several kilometers in the eastern and western sides of the Delta. Scenario six represents

  13. Ikaite solubility in seawater-derived brines at 1 atm and sub-zero temperatures to 265 K

    NASA Astrophysics Data System (ADS)

    Papadimitriou, Stathys; Kennedy, Hilary; Kennedy, Paul; Thomas, David N.

    2013-05-01

    The concentration-based (stoichiometric) equilibrium solubility product of ikaite (CaCO3·6H2O) in seawater and cryogenic seawater-derived brines was determined at 1 atm total pressure over the temperature range from -1.1 to -7.5 °C and the salinity range from 34 to 124 in temperature-salinity pairs representative of sea ice brines. The solubility measurements were obtained in solutions that were undersaturated and supersaturated with respect to ikaite by equilibration with CO2/N2 gas mixtures of known pCO2 (20-400 μatm). The solutions were then equilibrated with synthetic ikaite (seed) for up to 3 months in a closed system. Arrival of the solid-solution system at a long-term chemical equilibrium was indicated by attainment of constant chemical solution composition with respect to total dissolved calcium, total dissolved inorganic carbon, and total alkalinity. Using these measurements, the stoichiometric equilibrium solubility product of ikaite (Ksp,ikaite∗=[Ca][CO32-], in molkgsolution-2) was determined, with the carbonate ion concentration computed from the measured total alkalinity and total dissolved inorganic carbon concentrations. The computed carbonate ion concentration and, by extension, the Ksp,ikaite∗ are both contingent on solving the system of equations that describe the parameters of the CO2 system in seawater by extrapolation to the experimental salinity and temperature conditions. The results show that the pKsp,ikaite∗=-logKsp,ikaite∗ in seawater of salinity 34 at -1.1 °C was 5.362 ± 0.004 and that the pKsp,ikaite∗ in sea ice at the freezing point of brines of salinity greater than 34 can be described as a function of temperature (T, in K) by the equation, pKsp,ikaite∗=-15489.09608+623443.70216T-1+2355.14596lnT, in the temperature range of 265.15 K < T < 271.15 K (-8 °C < t < -2 °C). Brines of low pCO2 (20 μatm) yielded a much slower (>1 month) approach to chemical equilibrium when incubated without seeding ikaite crystals. Simple

  14. Arctic Sea Ice Is Losing Its Bulwark Against Warming Summers

    NASA Image and Video Library

    2017-12-08

    Arctic sea ice, the vast sheath of frozen seawater floating on the Arctic Ocean and its neighboring seas, has been hit with a double whammy over the past decades: as its extent shrunk, the oldest and thickest ice has either thinned or melted away, leaving the sea ice cap more vulnerable to the warming ocean and atmosphere. “What we’ve seen over the years is that the older ice is disappearing,” said Walt Meier, a sea ice researcher at NASA’s Goddard Space Flight Center in Greenbelt, Maryland. “This older, thicker ice is like the bulwark of sea ice: a warm summer will melt all the young, thin ice away but it can’t completely get rid of the older ice. But this older ice is becoming weaker because there’s less of it and the remaining old ice is more broken up and thinner, so that bulwark is not as good as it used to be.” Read more: go.nasa.gov/2dPJ9zT NASA image use policy. NASA Goddard Space Flight Center enables NASA’s mission through four scientific endeavors: Earth Science, Heliophysics, Solar System Exploration, and Astrophysics. Goddard plays a leading role in NASA’s accomplishments by contributing compelling scientific knowledge to advance the Agency’s mission. Follow us on Twitter Like us on Facebook Find us on Instagram

  15. Secular decline of seawater calcium increases seawater buffering and pH

    NASA Astrophysics Data System (ADS)

    Hain, M.; Sigman, D. M.; Higgins, J. A.; Haug, G. H.

    2015-12-01

    Reconstructed changes in seawater calcium and magnesium concentration ([Ca2+], [Mg2+]) predictably affect the ocean's acid/base and carbon chemistry. Yet inaccurate formulations of chemical equilibrium "constants" are currently in use to account for these changes. Here we develop an efficient implementation of the MIAMI Ionic Interaction Model (Millero and Pierrot, 1998) to predict all chemical equilibrium constants required for carbon chemistry calculations under variable [Ca2+] and [Mg2+] (Hain et al., 2015). We investigate the impact of [Ca2+] and [Mg2+] on the relationships among the ocean's pH, CO2, dissolved inorganic carbon (DIC), saturation state of CaCO3 (Ω), and buffer capacity. Increasing [Ca2+] and/or [Mg2+] enhances "ion pairing," which increases seawater buffering by increasing the concentration ratio of total to "free" (uncomplexed) carbonate ion. An increase in [Ca2+], however, also causes a decline in carbonate ion to maintain a given Ω, thereby overwhelming the ion pairing effect and decreasing seawater buffering. Given the reconstructions of Eocene [Ca2+] and [Mg2+] ([Ca2+]~20mM; [Mg2+]~30 mM), Eocene seawater would have required essentially the same DIC as today to simultaneously explain a similar-to-modern Ω and the estimated Eocene atmospheric CO2 of ~1000 ppm. During the Cretaceous, at ~4 times modern [Ca2+], ocean buffering would have been at a minimum. Overall, during times of high seawater [Ca2+], CaCO3 saturation, pH, and atmospheric CO2 were more susceptible to perturbations of the global carbon cycle. For example, given both Eocene and Cretaceous seawater [Ca2+] and [Mg2+], a doubling of atmospheric CO2 would require less carbon addition to the ocean/atmosphere system than under modern seawater composition. Moreover, increase in seawater buffering since the Cretaceous may have been a driver of evolution by raising energetic demands of biologically controlled calcification and CO2 concentration mechanisms that aid photosynthesis.

  16. The evolution of Phanerozoic seawater - Isotope paleothermometry finds consensus on Early Paleozoic warmth and constant seawater δ18O

    NASA Astrophysics Data System (ADS)

    Grossman, E. L.; Henkes, G. A.; Passey, B. H.; Shenton, B.; Yancey, T. E.; Perez-Huerta, A.

    2015-12-01

    Evolution of metazoan life is closely linked to the Phanerozoic evolution of ocean temperatures and chemistry. Oxygen isotopic evidence for early Phanerozoic paleotemperatures has been equivocal, with decreasing δ18O values with age being interpreted as warmer early oceans, decreasing seawater δ18O with age, or increasing diagenetic alteration in older samples. Here we compare an updated compilation of oxygen isotope data for carbonate and phosphate fossils and microfossils (Grossman, 2012, Geol. Time Scale, Elsevier, 195-220) with a compilation of new and existing clumped isotope data. Importantly, these data are curated based on sample preservation with special consideration given to screening techniques, and tectonic and burial history. Burial history is critical in the preservation of carbonate clumped isotope temperatures in particular, which can undergo reordering in the solid state. We use a model derived for reordering kinetics (Henkes et al., 2014, Geochim. Cosmochim. Acta 139:362-382) to screen clumped isotope data for the effects of solid-state burial alteration. With minor but significant exceptions (Late Cretaceous, Early Triassic), average δ18O values (4 m.y. window, 2 m.y. steps) for post-Devonian brachiopods, belemnites, and foraminifera, representing tropical-subtropical surface ocean conditions, yield average isotopic temperatures below 30°C (assuming a seawater δ18O value [ -1‰ VSMOW] of an "ice-free" world). In contrast, Ordovician to Devonian data show sustained temperatures of 35-40°C. Likewise, isotopic paleotemperatures from conodont apatite, known to be resistant to isotopic exchange, follow the same pattern. Clumped isotope data derived from Paleozoic brachiopod shells that experienced minimal burial (< 100 °C) and <1% reordering according to the taxon-specific clumped isotope reordering model yield typical temperatures of 25-30°C for the Carboniferous, and 35-40°C for the Ordovician-Silurian. Inserting clumped temperatures and

  17. The characteristics of dissolved organic matter (DOM) and chromophoric dissolved organic matter (CDOM) in Antarctic sea ice

    NASA Astrophysics Data System (ADS)

    Norman, Louiza; Thomas, David N.; Stedmon, Colin A.; Granskog, Mats A.; Papadimitriou, Stathys; Krapp, Rupert H.; Meiners, Klaus M.; Lannuzel, Delphine; van der Merwe, Pier; Dieckmann, Gerhard S.

    2011-05-01

    An investigation of coloured dissolved organic matter (CDOM) and its relationships to physical and biogeochemical parameters in Antarctic sea ice and oceanic water have indicated that ice melt may both alter the spectral characteristics of CDOM in Antarctic surface waters and serve as a likely source of fresh autochthonous CDOM and labile DOC. Samples were collected from melted bulk sea ice, sea ice brines, surface gap layer waters, and seawater during three expeditions: one during the spring to summer and two during the winter to spring transition period. Variability in both physical (temperature and salinity) and biogeochemical parameters (dissolved and particulate organic carbon and nitrogen, as well as chlorophyll a) was observed during and between studies, but CDOM absorption coefficients measured at 375 nm (a 375) did not differ significantly. Distinct peaked absorption spectra were consistently observed for bulk ice, brine, and gap water, but were absent in the seawater samples. Correlation with the measured physical and biogeochemical parameters could not resolve the source of these peaks, but the shoulders and peaks observed between 260 and 280 nm and between 320 to 330 nm respectively, particularly in the samples taken from high light-exposed gap layer environment, suggest a possible link to aromatic and mycosporine-like amino acids. Sea ice CDOM susceptibility to photo-bleaching was demonstrated in an in situ 120 hour exposure, during which we observed a loss in CDOM absorption of 53% at 280 nm, 58% at 330 nm, and 30% at 375 nm. No overall coincidental loss of DOC or DON was measured during the experimental period. A relationship between the spectral slope (S) and carbon-specific absorption (a *375) indicated that the characteristics of CDOM can be described by the mixing of two broad end-members; and aged material, present in brine and seawater samples characterised by high S values and low a *375; and a fresh material, due to elevated in situ

  18. Overview and Brief History of the Boron Isotope Proxy for Past Seawater pH

    NASA Astrophysics Data System (ADS)

    Hoenisch, B.; Hemming, G.

    2007-05-01

    In 1992 Hemming and Hanson (GCA, vol. 56, p. 537-543) showed that a variety of modern marine carbonates revealed a boron isotopic composition close to the isotopic composition of dissolved borate at modern seawater pH, suggesting this was the boron species preferentially adsorbed and incorporated into marine carbonates. With a constant offset between the trigonal and tetrahedrally coordinated boron species and a pH-dependent variation in their fractions, it appeared that this system would be sensitive to pH changes in the natural range of seawater. Accordingly, it was suggested that the boron isotope composition of marine carbonates is a proxy for past seawater pH. Subsequent culture studies with living planktic foraminifers and corals, as well as synthetic precipitation experiments confirmed that the boron isotopic composition follows the isotopic composition of borate across a wide range of seawater pH. In order to use the proxy with confidence, however, all other controls apart from pH need to be thoroughly understood. Recent laboratory and sediment experiments have demonstrated that vital effects and partial shell dissolution have the potential to modify the primary seawater pH signal recorded in the boron isotopic composition of planktic foraminifers. However it has also been shown that careful sample selection allows for avoiding these potential complications. A record of reconstructed surface seawater pH and estimated aqueous PCO2 shows a remarkable match between boron isotope based atmospheric pCO2 estimates and the Vostok ice core CO2 record. This convincingly demonstrates that boron isotopes in planktic foraminifers allow quantitative estimates of atmospheric pCO2 in the past, and confirms that glacial surface ocean pH was ~0.2 units higher compared to interglacial periods. We are going to review and discuss the achievements generated in Gil Hanson's lab over the past 15 years in the light of recent empirical measurements of the boron isotope

  19. Enhanced water vapour flow in silica microchannels and interdiffusive water vapour flow through anodic aluminium oxide (AAO) membranes

    NASA Astrophysics Data System (ADS)

    Lei, Wenwen; McKenzie, David R.

    2015-12-01

    Enhanced liquid water flows through carbon nanotubes reinvigorated the study of moisture permeation through membranes and micro- and nano-channels. The study of water vapour through micro-and nano-channels has been neglected even though water vapour is as important as liquid water for industry, especially for encapsulation of electronic devices. Here we measure moisture flow rates in silica microchannels and interdiffusive water vapour flows in anodic aluminium oxide (AAO) membrane channels for the first time. We construct theory for the flow rates of the dominant modes of water transport through four previously defined standard configurations and benchmark it against our new measurements. The findings show that measurements of leak behaviour made using other molecules, such as helium, are not reliable. Single phase water vapour flow is overestimated by a helium measurement, while Washburn or capillary flow is underestimated or for all channels when boundary slip applies, to an extent that depends on the slip length for the liquid phase flows.

  20. Atomic origins of water-vapour-promoted alloy oxidation

    NASA Astrophysics Data System (ADS)

    Luo, Langli; Su, Mao; Yan, Pengfei; Zou, Lianfeng; Schreiber, Daniel K.; Baer, Donald R.; Zhu, Zihua; Zhou, Guangwen; Wang, Yanting; Bruemmer, Stephen M.; Xu, Zhijie; Wang, Chongmin

    2018-06-01

    The presence of water vapour, intentional or unavoidable, is crucial to many materials applications, such as in steam generators, turbine engines, fuel cells, catalysts and corrosion1-4. Phenomenologically, water vapour has been noted to accelerate oxidation of metals and alloys5,6. However, the atomistic mechanisms behind such oxidation remain elusive. Through direct in situ atomic-scale transmission electron microscopy observations and density functional theory calculations, we reveal that water-vapour-enhanced oxidation of a nickel-chromium alloy is associated with proton-dissolution-promoted formation, migration, and clustering of both cation and anion vacancies. Protons derived from water dissociation can occupy interstitial positions in the oxide lattice, consequently lowering vacancy formation energy and decreasing the diffusion barrier of both cations and anions, which leads to enhanced oxidation in moist environments at elevated temperatures. This work provides insights into water-vapour-enhanced alloy oxidation and has significant implications in other material and chemical processes involving water vapour, such as corrosion, heterogeneous catalysis and ionic conduction.

  1. Atomic origins of water-vapour-promoted alloy oxidation.

    PubMed

    Luo, Langli; Su, Mao; Yan, Pengfei; Zou, Lianfeng; Schreiber, Daniel K; Baer, Donald R; Zhu, Zihua; Zhou, Guangwen; Wang, Yanting; Bruemmer, Stephen M; Xu, Zhijie; Wang, Chongmin

    2018-06-01

    The presence of water vapour, intentional or unavoidable, is crucial to many materials applications, such as in steam generators, turbine engines, fuel cells, catalysts and corrosion 1-4 . Phenomenologically, water vapour has been noted to accelerate oxidation of metals and alloys 5,6 . However, the atomistic mechanisms behind such oxidation remain elusive. Through direct in situ atomic-scale transmission electron microscopy observations and density functional theory calculations, we reveal that water-vapour-enhanced oxidation of a nickel-chromium alloy is associated with proton-dissolution-promoted formation, migration, and clustering of both cation and anion vacancies. Protons derived from water dissociation can occupy interstitial positions in the oxide lattice, consequently lowering vacancy formation energy and decreasing the diffusion barrier of both cations and anions, which leads to enhanced oxidation in moist environments at elevated temperatures. This work provides insights into water-vapour-enhanced alloy oxidation and has significant implications in other material and chemical processes involving water vapour, such as corrosion, heterogeneous catalysis and ionic conduction.

  2. The ignitability of petrol vapours and potential for vapour phase explosion by use of TASER® law enforcement electronic control device.

    PubMed

    Clarke, C; Andrews, S P

    2014-12-01

    An experimental study was made of the potential of the TASER-X26™ law enforcement electronic control device to ignite petrol vapours if used by an officer to incapacitate a person soaked in petrol, or within a flammable atmosphere containing petrol vapour. Bench scale tests have shown that a wooden mannequin with pig skin covering the chest was a suitable representation of a human target. Full scale tests using the mannequin have shown that the arc from a TASER-X26™ is capable of igniting petrol/air vapours on a petrol-soaked person. Further tests in a 1/5 scale and a full scale compartment have shown that if a TASER is used within a compartment, a petrol vapour explosion (deflagration) may be achieved. It is evident from this research that if used in a flammable vapour rich environment, the device could prove fatal not only to the target but the TASER® operator as well. Copyright © 2014 Forensic Science Society. Published by Elsevier Ireland Ltd. All rights reserved.

  3. Responses of Baltic Sea Ice and Open-Water Natural Bacterial Communities to Salinity Change

    PubMed Central

    Kaartokallio, Hermanni; Laamanen, Maria; Sivonen, Kaarina

    2005-01-01

    To investigate the responses of Baltic Sea wintertime bacterial communities to changing salinity (5 to 26 practical salinity units), an experimental study was conducted. Bacterial communities of Baltic seawater and sea ice from a coastal site in southwest Finland were used in two batch culture experiments run for 17 or 18 days at 0°C. Bacterial abundance, cell volume, and leucine and thymidine incorporation were measured during the experiments. The bacterial community structure was assessed using denaturing gradient gel electrophoresis (DGGE) of PCR-amplified partial 16S rRNA genes with sequencing of DGGE bands from initial communities and communities of day 10 or 13 of the experiment. The sea ice-derived bacterial community was metabolically more active than the open-water community at the start of the experiment. Ice-derived bacterial communities were able to adapt to salinity change with smaller effects on physiology and community structure, whereas in the open-water bacterial communities, the bacterial cell volume evolution, bacterial abundance, and community structure responses indicated the presence of salinity stress. The closest relatives for all eight partial 16S rRNA gene sequences obtained were either organisms found in polar sea ice and other cold habitats or those found in summertime Baltic seawater. All sequences except one were associated with the α- and γ-proteobacteria or the Cytophaga-Flavobacterium-Bacteroides group. The overall physiological and community structure responses were parallel in ice-derived and open-water bacterial assemblages, which points to a linkage between community structure and physiology. These results support previous assumptions of the role of salinity fluctuation as a major selective factor shaping the sea ice bacterial community structure. PMID:16085826

  4. Development and validation of a method for mercury determination in seawater for the process control of a candidate certified reference material.

    PubMed

    Sánchez, Raquel; Snell, James; Held, Andrea; Emons, Hendrik

    2015-08-01

    A simple, robust and reliable method for mercury determination in seawater matrices based on the combination of cold vapour generation and inductively coupled plasma mass spectrometry (CV-ICP-MS) and its complete in-house validation are described. The method validation covers parameters such as linearity, limit of detection (LOD), limit of quantification (LOQ), trueness, repeatability, intermediate precision and robustness. A calibration curve covering the whole working range was achieved with coefficients of determination typically higher than 0.9992. The repeatability of the method (RSDrep) was 0.5 %, and the intermediate precision was 2.3 % at the target mass fraction of 20 ng/kg. Moreover, the method was robust with respect to the salinity of the seawater. The limit of quantification was 2.7 ng/kg, which corresponds to 13.5 % of the target mass fraction in the future certified reference material (20 ng/kg). An uncertainty budget for the measurement of mercury in seawater has been established. The relative expanded (k = 2) combined uncertainty is 6 %. The performance of the validated method was demonstrated by generating results for process control and a homogeneity study for the production of a candidate certified reference material.

  5. The application of remote sensing image sea ice monitoring method in Bohai Bay based on C4.5 decision tree algorithm

    NASA Astrophysics Data System (ADS)

    Ye, Wei; Song, Wei

    2018-02-01

    In The Paper, the remote sensing monitoring of sea ice problem was turned into a classification problem in data mining. Based on the statistic of the related band data of HJ1B remote sensing images, the main bands of HJ1B images related with the reflectance of seawater and sea ice were found. On the basis, the decision tree rules for sea ice monitoring were constructed by the related bands found above, and then the rules were applied to Liaodong Bay area seriously covered by sea ice for sea ice monitoring. The result proved that the method is effective.

  6. Periodic bedforms generated by sublimation on terrestrial and martian ice sheets under the influence of the turbulent atmospheric boundary layer

    NASA Astrophysics Data System (ADS)

    Bordiec, Maï; Carpy, Sabrina; Perret, Laurent; Bourgeois, Olivier; Massé, Marion

    2017-04-01

    The redistribution of surface ice induced the wind flow may lead to the development and migration of periodic bedforms, or "ice ripples", at the surface of ice sheets. In certain cold and dry environments, this redistribution need not involve solid particle transport but may be dominated by sublimation and condensation, inducing mass transfers between the ice surface and the overlying steady boundary layer turbulent flow. These mass transfers diffuse the water vapour sublimated from the ice into the atmosphere and become responsible for the amplification and propagation of ripples in a direction perpendicular to their crests. Such ice ripples, 24 cm in wavelength, have been described in the so-called Blue Ice Areas of Antarctica. In order to understand the mechanisms that generate and develop these periodic bedforms on terrestrial glaciers and to evaluate the plausibility that similar bedforms may develop on Mars, we performed a linear stability analysis applied to a turbulent boundary layer flow perturbed by a wavy ice surface. The model is developed as follow. We first solve the flow dynamics using numerical methods analogous to those used in sand wave models assuming that the airflow is similar in both problems. We then add the transport/diffusion equation of water vapour following the same scheme. We use the Reynolds-averaged description of the equation with a Prandtl-like closure. We insert a damping term in the exponential formula of the Van Driest mixing length, depending on the pressure gradient felt by the flow and related to the thickness of the viscous sublayer at the ice-atmosphere interface. This formulation is an efficient way to properly represent the transitional regime under which the ripples grow. Once the mass flux of water vapour is solved, the phase shift between the ripples crests and the maximum of the flux can be deduced for different environments. The temporal evolution of the ice surface can be expressed from these quantities to infer the

  7. Dynamic Antarctic ice sheet during the early to mid-Miocene

    PubMed Central

    DeConto, Robert M.; Pollard, David; Levy, Richard H.

    2016-01-01

    Geological data indicate that there were major variations in Antarctic ice sheet volume and extent during the early to mid-Miocene. Simulating such large-scale changes is problematic because of a strong hysteresis effect, which results in stability once the ice sheets have reached continental size. A relatively narrow range of atmospheric CO2 concentrations indicated by proxy records exacerbates this problem. Here, we are able to simulate large-scale variability of the early to mid-Miocene Antarctic ice sheet because of three developments in our modeling approach. (i) We use a climate–ice sheet coupling method utilizing a high-resolution atmospheric component to account for ice sheet–climate feedbacks. (ii) The ice sheet model includes recently proposed mechanisms for retreat into deep subglacial basins caused by ice-cliff failure and ice-shelf hydrofracture. (iii) We account for changes in the oxygen isotopic composition of the ice sheet by using isotope-enabled climate and ice sheet models. We compare our modeling results with ice-proximal records emerging from a sedimentological drill core from the Ross Sea (Andrill-2A) that is presented in a companion article. The variability in Antarctic ice volume that we simulate is equivalent to a seawater oxygen isotope signal of 0.52–0.66‰, or a sea level equivalent change of 30–36 m, for a range of atmospheric CO2 between 280 and 500 ppm and a changing astronomical configuration. This result represents a substantial advance in resolving the long-standing model data conflict of Miocene Antarctic ice sheet and sea level variability. PMID:26903645

  8. Saltwater icephobicity: Influence of surface chemistry on saltwater icing

    PubMed Central

    Carpenter, Katherine; Bahadur, Vaibhav

    2015-01-01

    Most studies on icephobicity focus on ice formation with pure water. This manuscript presents studies to understand the influence of surfaces on saltwater ice nucleation and propagation. Experiments are conducted to quantify the influence of surface chemistry on saltwater ice nucleation and to understand the utility of superhydrophobic surfaces for saltwater icephobicity. These experiments are conducted with pure water and two sodium chloride solutions, which represent the salinity of seawater and briny produced water. It is seen that the presence of salt slows down the ice front propagation velocity significantly. Saltwater droplet impact dynamics on superhydrophobic surfaces are also different from pure water. Saltwater droplets retract more and a greater fraction of impacting liquid is repelled from the superhydrophobic surface. It is seen that the greater bounciness of saltwater droplets is a result of slower ice nucleation propagation kinetics. These experiments indicate that superhydrophobic surfaces will have better resistance to impact icing with saltwater than pure water and can remain useful at temperatures as low as −40 °C. Overall, this work is a starting point for further studies on heterogeneous nucleation in saltwater and serves as a bridge between the widely studied freshwater icephobic surfaces and saltwater-related applications. PMID:26626958

  9. Water Vapour Effects in Mass Measurement

    NASA Astrophysics Data System (ADS)

    Khélifa, N.

    2008-01-01

    Water vapour density inside the mass comparator enclosure is a critical parameter whose fluctuations during mass weighing can lead to errors in the determination of an unknown mass. To monitor them, a method using DFB laser diode in the near infrared has been proposed and tested. Preliminary results of our observation of water vapour sorption and de-sorption processes from the walls and the mass standard are reported.

  10. Reviews and syntheses: Ice acidification, the effects of ocean acidification on sea ice microbial communities

    NASA Astrophysics Data System (ADS)

    McMinn, Andrew

    2017-09-01

    a major contribution to sea ice productivity will depend not only on their ability to survive in the ice but also on their ability to survive the increasing seawater temperatures, changing distribution of nutrients and declining pH forecast for the water column over the next centuries.

  11. New method to assess the water vapour permeance of wound coverings.

    PubMed

    Jonkman, M F; Molenaar, I; Nieuwenhuis, P; Bruin, P; Pennings, A J

    1988-05-01

    A new method for assessing the permeability to water vapour of wound coverings is presented, using the evaporimeter developed by Nilsson. This new method combines the water vapour transmission rate (WVTR) and the vapour pressure difference across a wound covering in one absolute measure: the water vapour permeance (WVP). The WVP of a wound covering is the steady flow (g) of water vapour per unit (m2) area of surface in unit (h) time induced by unit (kPa) vapour pressure difference, g.m-2.h-1.kPa-1. Since the WVP of a wound covering is a more accurate measure for the permeability than the WVTR is, it facilitates the prediction of the water exchange of a wound covering in clinical situations.

  12. SRB seawater corrosion project

    NASA Technical Reports Server (NTRS)

    Bozack, M. J.

    1991-01-01

    The corrosion behavior of 2219 aluminum when exposed to seawater was characterized. Controlled corrosion experiments at three different temperatures (30, 60 and 100 C) and two different environments (seawater and 3.5 percent salt solution) were designed to elucidate the initial stages in the corrosion process. It was found that 2219 aluminum is an active catalytic surface for growth of Al2O3, NaCl, and MgO. Formation of Al2O3 is favored at lower temperatures, while MgO is favored at higher temperatures. Visible corrosion products are formed within 30 minutes after seawater exposure. Corrosion characteristics in 3.5 percent salt solution are different than corrosion in seawater. Techniques utilized were: (1) scanning electron microscopy, (2) energy dispersive x-ray spectroscopy, and (3) Auger electron spectroscopy.

  13. Geoengineering by cloud seeding: influence on sea ice and climate system

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

    Rasch, Philip J.; Latham, John; Chen, Chih-Chieh

    2009-12-18

    GCM computations using a fully coupled ocean atmosphere model indicate that increasing cloud reflectivity by seeding maritime boundary layer clouds with particles made from seawater may compensate for some of the effects on climate of increasing greenhouse gas concentrations. The chosen seeding strategy (one of many possible scenarios) can restore global averages of temperature, precipitation and sea ice to present day values, but not simultaneously. The response varies nonlinearly with extent of the seeding, and geoengineering generates local changes to important climatic features. The global tradeoffs of restoring ice cover and cooling the planet must be assessed alongside the localmore » changes to climate features.« less

  14. Medical cannabis use in Canada: vapourization and modes of delivery.

    PubMed

    Shiplo, Samantha; Asbridge, Mark; Leatherdale, Scott T; Hammond, David

    2016-10-29

    The mode of medical cannabis delivery-whether cannabis is smoked, vapourized, or consumed orally-may have important implications for its therapeutic efficacy and health risks. However, there is very little evidence on current patterns of use among Canadian medical cannabis users, particularly with respect to modes of delivery. The current study examined modes of medical cannabis delivery following regulatory changes in 2014 governing how Canadians access medical cannabis. A total of 364 approved adult Canadian medical cannabis users completed an online cross-sectional survey between April and June 2015. The survey examined patterns of medical cannabis use, modes of delivery used, and reasons for use. Participants were recruited through a convenience sample from nine Health Canada licensed producers. Using a vapourizer was the most popular mode of delivery for medical cannabis (53 %), followed by smoking a joint (47 %). The main reason for using a vapourizer was to reduce negative health consequences associated with smoking. A majority of current vapourizer users reported using a portable vapourizer (67.2 %), followed by a stationary vapourizer (41.7 %), and an e-cigarette or vape pen (19.3 %). Current use of a vapourizer was associated with fewer respiratory symptoms (AOR = 1.28, 95 % CI 1.05-1.56, p = 0.01). The findings suggest an increase in the popularity of vapourizers as the primary mode of delivery among approved medical users. Using vapourizers has the potential to prevent some of the adverse respiratory health consequences associated with smoking and may serve as an effective harm reduction method. Monitoring implications of such current and future changes to medical cannabis regulations may be beneficial to policymakers.

  15. Snow contribution to first-year and second-year Arctic sea ice mass balance north of Svalbard

    NASA Astrophysics Data System (ADS)

    Granskog, Mats A.; Rösel, Anja; Dodd, Paul A.; Divine, Dmitry; Gerland, Sebastian; Martma, Tõnu; Leng, Melanie J.

    2017-03-01

    The salinity and water oxygen isotope composition (δ18O) of 29 first-year (FYI) and second-year (SYI) Arctic sea ice cores (total length 32.0 m) from the drifting ice pack north of Svalbard were examined to quantify the contribution of snow to sea ice mass. Five cores (total length 6.4 m) were analyzed for their structural composition, showing variable contribution of 10-30% by granular ice. In these cores, snow had been entrained in 6-28% of the total ice thickness. We found evidence of snow contribution in about three quarters of the sea ice cores, when surface granular layers had very low δ18O values. Snow contributed 7.5-9.7% to sea ice mass balance on average (including also cores with no snow) based on δ18O mass balance calculations. In SYI cores, snow fraction by mass (12.7-16.3%) was much higher than in FYI cores (3.3-4.4%), while the bulk salinity of FYI (4.9) was distinctively higher than for SYI (2.7). We conclude that oxygen isotopes and salinity profiles can give information on the age of the ice and enables distinction between FYI and SYI (or older) ice in the area north of Svalbard.Plain Language SummaryThe role of snow in sea <span class="hlt">ice</span> mass balance is largely two fold. Firstly, it can slow down growth and melt due to its high insulation and high reflectance, but secondly it can actually contribute to sea <span class="hlt">ice</span> growth if the snow cover is turned into <span class="hlt">ice</span>. The latter is largely a consequence of high mass of snow on top of sea <span class="hlt">ice</span> that can push the surface of the sea <span class="hlt">ice</span> below sea level and <span class="hlt">seawater</span> can flood the <span class="hlt">ice</span>. This mixture of <span class="hlt">seawater</span> and snow can then freeze and add to the growth of sea <span class="hlt">ice</span>. This is very typical in the Antarctic but not believed to be so important in the Arctic. In this work we show, for the first time, that snow actually contributes significantly to the growth of Arctic sea <span class="hlt">ice</span>. This is likely a consequence of the thinning of the Arctic sea <span class="hlt">ice</span>. The conditions in the Arctic, with</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27780352','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27780352"><span>Seasonal Study of Mercury Species in the Antarctic Sea <span class="hlt">Ice</span> Environment.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Nerentorp Mastromonaco, Michelle G; Gårdfeldt, Katarina; Langer, Sarka; Dommergue, Aurélien</p> <p>2016-12-06</p> <p>Limited studies have been conducted on mercury concentrations in the polar cryosphere and the factors affecting the distribution of mercury within sea <span class="hlt">ice</span> and snow are poorly understood. Here we present the first comprehensive seasonal study of elemental and total mercury concentrations in the Antarctic sea <span class="hlt">ice</span> environment covering data from measurements in air, sea <span class="hlt">ice</span>, <span class="hlt">seawater</span>, snow, frost flowers, and brine. The average concentration of total mercury in sea <span class="hlt">ice</span> decreased from winter (9.7 ng L -1 ) to spring (4.7 ng L -1 ) while the average elemental mercury concentration increased from winter (0.07 ng L -1 ) to summer (0.105 ng L -1 ). The opposite trends suggest potential photo- or dark oxidation/reduction processes within the <span class="hlt">ice</span> and an eventual loss of mercury via brine drainage or gas evasion of elemental mercury. Our results indicate a seasonal variation of mercury species in the polar sea <span class="hlt">ice</span> environment probably due to varying factors such as solar radiation, temperature, brine volume, and atmospheric deposition. This study shows that the sea <span class="hlt">ice</span> environment is a significant interphase between the polar ocean and the atmosphere and should be accounted for when studying how climate change may affect the mercury cycle in polar regions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009EGUGA..11.5164V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009EGUGA..11.5164V"><span>On the brine drainage and algal uptake controls of the nutrient supply to the sea <span class="hlt">ice</span> interior</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Vancoppenolle, M.; Goosse, H.; de Montety, A.; Fichefet, T.; Tison, J.-L.</p> <p>2009-04-01</p> <p>Sea <span class="hlt">ice</span> ecosystems are important components of the biogeochemical cycles (including carbon) and hence have a potential impact on climate. They are characterized by large stocks of micro-algae. Those algae (mostly diatoms) live in liquid inclusions of saline brine, which are encased within the solid <span class="hlt">ice</span> matrix and require sustained nutrient supply to grow. In this study, we investigate the interactions between nutrients, brine motion and algal growth, using a one-dimensional (1D) sea <span class="hlt">ice</span> model. The model includes (i) a classical formulation for snow and <span class="hlt">ice</span> thermodynamics with explicit, reformulated brine physics and (ii) an idealized sea <span class="hlt">ice</span> biological component, characterized by one single nutrient, namely dissolved silica (DSi), which stocks are reduced by a prescribed primary production. DSi is considered as a passive tracer dissolved within brine following fluid motion. The brine flow regime (advective, diffusive or turbulent) is computed as a function of environmental <span class="hlt">ice</span> conditions. In winter, a Rayleigh number proposed by Notz and Worster (2008) is used to differentiate diffusion and convection. <span class="hlt">Ice</span> salinity and DSi concentrations within the <span class="hlt">ice</span> are solutions of 1D advection-diffusion equations over the variable volume brine network domain. The model is configured for a typical year of seasonal Weddell Sea <span class="hlt">ice</span>. The simulated vertical salinity and tracer profiles as well as <span class="hlt">ice</span>-ocean salt fluxes realistically agree with observations. Complex bio-physical interactions are simulated by the model. Analysis highlights the role of convection in the lowermost 5-10 cm of <span class="hlt">ice</span> (gravity drainage), mixing highly saline, nutrient-depleted brine with comparatively fresh, nutrient-rich <span class="hlt">seawater</span>. Hence, gravity drainage rejects salt to the ocean and provides nutrients to the <span class="hlt">ice</span> interior. In turn, primary production and brine convection act synergetically to form a nutrient pump, which enhances the net ocean-to-<span class="hlt">ice</span> DSi flux by 20-115%, compared to an abiotic situation. The</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25143114','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25143114"><span>A microbial ecosystem beneath the West Antarctic <span class="hlt">ice</span> sheet.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Christner, Brent C; Priscu, John C; Achberger, Amanda M; Barbante, Carlo; Carter, Sasha P; Christianson, Knut; Michaud, Alexander B; Mikucki, Jill A; Mitchell, Andrew C; Skidmore, Mark L; Vick-Majors, Trista J</p> <p>2014-08-21</p> <p>Liquid water has been known to occur beneath the Antarctic <span class="hlt">ice</span> sheet for more than 40 years, but only recently have these subglacial aqueous environments been recognized as microbial ecosystems that may influence biogeochemical transformations on a global scale. Here we present the first geomicrobiological description of water and surficial sediments obtained from direct sampling of a subglacial Antarctic lake. Subglacial Lake Whillans (SLW) lies beneath approximately 800 m of <span class="hlt">ice</span> on the lower portion of the Whillans <span class="hlt">Ice</span> Stream (WIS) in West Antarctica and is part of an extensive and evolving subglacial drainage network. The water column of SLW contained metabolically active microorganisms and was derived primarily from glacial <span class="hlt">ice</span> melt with solute sources from lithogenic weathering and a minor <span class="hlt">seawater</span> component. Heterotrophic and autotrophic production data together with small subunit ribosomal RNA gene sequencing and biogeochemical data indicate that SLW is a chemosynthetically driven ecosystem inhabited by a diverse assemblage of bacteria and archaea. Our results confirm that aquatic environments beneath the Antarctic <span class="hlt">ice</span> sheet support viable microbial ecosystems, corroborating previous reports suggesting that they contain globally relevant pools of carbon and microbes that can mobilize elements from the lithosphere and influence Southern Ocean geochemical and biological systems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018Cryo...90...70N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018Cryo...90...70N"><span>Prediction of <span class="hlt">vapour</span>-liquid and <span class="hlt">vapour</span>-liquid-liquid equilibria of nitrogen-hydrocarbon mixtures used in J-T refrigerators</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Narayanan, Vineed; Venkatarathnam, G.</p> <p>2018-03-01</p> <p>Nitrogen-hydrocarbon mixtures are widely used as refrigerants in J-T refrigerators operating with mixtures, as well as in natural gas liquefiers. The Peng-Robinson equation of state has traditionally been used to simulate the above cryogenic process. Multi parameter Helmholtz energy equations are now preferred for determining the properties of natural gas. They have, however, been used only to predict <span class="hlt">vapour</span>-liquid equilibria, and not <span class="hlt">vapour</span>-liquid-liquid equilibria that can occur in mixtures used in cryogenic mixed refrigerant processes. In this paper the <span class="hlt">vapour</span>-liquid equilibrium of binary mixtures of nitrogen-methane, nitrogen-ethane, nitrogen-propane, nitrogen-isobutane and three component mixtures of nitrogen-methane-ethane and nitrogen-methane-propane have been studied with the Peng-Robinson and the Helmholtz energy equations of state of NIST REFPROP and compared with experimental data available in the literature.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25759005','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25759005"><span>Superhydrophobic surfaces for applications in <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ferrari, Michele; Benedetti, Alessandro</p> <p>2015-08-01</p> <p>Technological fields in which <span class="hlt">seawater</span> is implied are numerorus, working in <span class="hlt">seawater</span> (shipping, oil industry, marine aquaculture,..), and exploiting <span class="hlt">seawater</span> in plants (cooling heat-exchange, desalination, power plants,..). All suffer from detrimental effects induced by biofouling mainly enhancing material failures and limiting energetic efficiencies. Among the remediation solutions, technologies coniugating economical, green and efficiency criteria should represent the direction. With the aim to meet these criteria, superhydrophobic (SH) technology attracted many researches for the protection of materials operating in contact with <span class="hlt">seawater</span>. In this work, the literature focusing on such technology for the protection of surfaces in contact with <span class="hlt">seawater</span> has been reviewed, mainly focusing on boat and ship hull protection. Despite the growing interest around SH technology in <span class="hlt">seawater</span> for fouling control and friction drag reduction of hulls, to date literature shows that superhydrophobicity in <span class="hlt">seawater</span> is still limited if compared with a time window compatible with technological needs (set on years). An evaluation of the causes of early superhydrophobicity loss under operative conditions clearly indicates that, to the best of present knowledge, a SH surface cannot preserve this feature by itself alone (especially in real <span class="hlt">seawater</span>). Hence, we have considered to highlight the behaviour of SH surfaces in <span class="hlt">seawater</span> in relation to early stages of biocolonization (conditioning film and pioneering bioslime formation). Considering the annual costs sustained for the biofouling impact control, advantages coming from SH surfaces, in terms of foul control and friction drag reduction, would allow economical savings allowing to cover both the appliance of longevity keeping strategies of the SH surfaces and investments in green technologies of SH coating life cycle (production, storing). In addition a brief outlook is provided on technological fields exploiting <span class="hlt">seawater</span> in pipelines</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_4");'>4</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li class="active"><span>6</span></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_6 --> <div id="page_7" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li class="active"><span>7</span></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="121"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29440667','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29440667"><span>Poleward upgliding Siberian atmospheric rivers over sea <span class="hlt">ice</span> heat up Arctic upper air.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Komatsu, Kensuke K; Alexeev, Vladimir A; Repina, Irina A; Tachibana, Yoshihiro</p> <p>2018-02-13</p> <p>We carried out upper air measurements with radiosondes during the summer over the Arctic Ocean from an icebreaker moving poleward from an <span class="hlt">ice</span>-free region, through the <span class="hlt">ice</span> edge, and into a region of thick <span class="hlt">ice</span>. Rapid warming of the Arctic is a significant environmental issue that occurs not only at the surface but also throughout the troposphere. In addition to the widely accepted mechanisms responsible for the increase of tropospheric warming during the summer over the Arctic, we showed a new potential contributing process to the increase, based on our direct observations and supporting numerical simulations and statistical analyses using a long-term reanalysis dataset. We refer to this new process as "Siberian Atmospheric Rivers (SARs)". Poleward upglides of SARs over cold air domes overlying sea <span class="hlt">ice</span> provide the upper atmosphere with extra heat via condensation of water <span class="hlt">vapour</span>. This heating drives increased buoyancy and further strengthens the ascent and heating of the mid-troposphere. This process requires the combination of SARs and sea <span class="hlt">ice</span> as a land-ocean-atmosphere system, the implication being that large-scale heat and moisture transport from the lower latitudes can remotely amplify the warming of the Arctic troposphere in the summer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=203895','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=203895"><span>Changes in Escherichia coli cells starved in <span class="hlt">seawater</span> or grown in <span class="hlt">seawater</span>-wastewater mixtures.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Munro, P M; Gauthier, M J; Laumond, F M</p> <p>1987-01-01</p> <p>Some metabolic modifications of Escherichia coli cells during starvation in <span class="hlt">seawater</span> were studied in laboratory microcosms. The apparent die-off of this bacterium under such conditions, as observed by comparing the enumeration of CFU in conventional freshwater media and direct epifluorescence counts, was partially prevented when cells were previously grown in salted organic medium or on <span class="hlt">seawater</span>-wastewater agar. beta-Galactosidase activity of starved cells disappeared gradually with time, even though some other enzymatic activities, such as that of alkaline phosphatase, increased. Moreover, some modifications of sensitivity to antibiotics, heavy metals, and bacteriophages in <span class="hlt">seawater</span>- and wastewater-grown cells suggested that the cells undergo structural changes under natural marine conditions. These results provide additional experimental data indicating the possible active adaptation of E. coli cells to <span class="hlt">seawater</span>. PMID:3116927</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFMPP11E..02G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFMPP11E..02G"><span>Simulating a Dynamic Antarctic <span class="hlt">Ice</span> Sheet in the Early to Middle Miocene</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gasson, E.; DeConto, R.; Pollard, D.; Levy, R. H.</p> <p>2015-12-01</p> <p>There are a variety of sources of geological data that suggest major variations in the volume and extent of the Antarctic <span class="hlt">ice</span> sheet during the early to middle Miocene. Simulating such variability using coupled climate-<span class="hlt">ice</span> sheet models is problematic due to a strong hysteresis effect caused by height-mass balance feedback and albedo feedback. This results in limited retreat of the <span class="hlt">ice</span> sheet once it has reached the continental size, as likely occurred prior to the Miocene. Proxy records suggest a relatively narrow range of atmospheric CO2 during the early to middle Miocene, which exacerbates this problem. We use a new climate forcing which accounts for <span class="hlt">ice</span> sheet-climate feedbacks through an asynchronous GCM-RCM coupling, which is able to better resolve the narrow Antarctic ablation zone in warm climate simulations. When combined with recently suggested mechanisms for retreat into subglacial basins due to <span class="hlt">ice</span> shelf hydrofracture and <span class="hlt">ice</span> cliff failure, we are able to simulate large-scale variability of the Antarctic <span class="hlt">ice</span> sheet in the Miocene. This variability is equivalent to a <span class="hlt">seawater</span> oxygen isotope signal of ~0.5 ‰, or a sea level equivalent change of ~35 m, for a range of atmospheric CO2 between 280 - 500 ppm.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70024584','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70024584"><span>The major-ion composition of Silurian <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Brennan, S.T.; Lowenstein, T.K.</p> <p>2002-01-01</p> <p>One-hundred fluid inclusions in Silurian marine halite were analyzed in order to determine the major-ion composition of Silurian <span class="hlt">seawater</span>. The samples analyzed were from three formations in the Late Silurian Michigan Basin, the A-1, A-2, and B Evaporites of the Salina Group, and one formation in the Early Silurian Canning Basin (Australia), the Mallowa Salt of the Carribuddy Group. The results indicate that the major-ion composition of Silurian <span class="hlt">seawater</span> was not the same as present-day <span class="hlt">seawater</span>. The Silurian ocean had lower concentrations of Mg2+, Na+, and SO2-4, and much higher concentrations of Ca2+ relative to the ocean's present-day composition. Furthermore, Silurian <span class="hlt">seawater</span> had Ca2+ in excess of SO2-4. Evaporation of Silurian <span class="hlt">seawater</span> of the composition determined in this study produces KC1-type potash minerals that lack the MgSO4-type late stage salts formed during the evaporation of present-day <span class="hlt">seawater</span>. The relatively low Na+ concentrations in Silurian <span class="hlt">seawater</span> support the hypothesis that oscillations in the major-ion composition of the oceans are primarily controlled by changes in the flux of mid-ocean ridge brine and riverine inputs and not global or basin-scale, <span class="hlt">seawater</span>-driven dolomitization. The Mg2+/Ca2+ ratio of Silurian <span class="hlt">seawater</span> was ~1.4, and the K+/Ca2+ ratio was ~0.3, both of which differ from the present-day counterparts of 5 and 1, respectively. <span class="hlt">Seawaters</span> with Mg2+/Ca2+ 2 (e.g., modern <span class="hlt">seawater</span>) facilitate the precipitation of aragonite and high-magnesian calcite. Therefore, the early Paleozoic calcite seas were likely due to the low Mg2+/Ca2+ ratio of <span class="hlt">seawater</span>, not the pCO2 of the Silurian atmosphere. Copyright ?? 2002 Elsevier Science Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.G11D..08F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.G11D..08F"><span>Water storage in marine sediment and implications for inferences of past global <span class="hlt">ice</span> volume</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ferrier, K.; Li, Q.; Pico, T.; Austermann, J.</p> <p>2017-12-01</p> <p>Changes in past sea level are of wide interest because they provide information on the sensitivity of <span class="hlt">ice</span> sheets to climate change, and thus inform predictions of future sea-level change. Sea level changes are influenced by many processes, including the storage of water in sedimentary pore space. Here we use a recent extension of gravitationally self-consistent sea-level models to explore the effects of marine sedimentary water storage on the global <span class="hlt">seawater</span> balance and inferences of past global <span class="hlt">ice</span> volume. Our analysis suggests that sedimentary water storage can be a significant component of the global <span class="hlt">seawater</span> budget over the 105-year timescales associated with glacial-interglacial cycles, and an even larger component over longer timescales. Estimates of global sediment fluxes to the oceans suggest that neglecting marine sedimentary water storage may produce meter-scale errors in estimates of peak global mean sea level equivalent (GMSL) during the Last Interglacial (LIG). These calculations show that marine sedimentary water storage can be a significant contributor to the overall effects of sediment redistribution on sea-level change, and that neglecting sedimentary water storage can lead to substantial errors in inferences of global <span class="hlt">ice</span> volume at past interglacials. This highlights the importance of accounting for the influences of sediment fluxes and sedimentary water storage on sea-level change over glacial-interglacial timescales.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24349517','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24349517"><span>Edwardsiella andrillae, a new species of sea anemone from Antarctic <span class="hlt">ice</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Daly, Marymegan; Rack, Frank; Zook, Robert</p> <p>2013-01-01</p> <p>Exploration of the lower surface of the Ross <span class="hlt">Ice</span> Shelf in Antarctica by the Submersible Capable of under-<span class="hlt">Ice</span> Navigation and Imaging (SCINI) remotely operated vehicle discovered a new species of sea anemone living in this previously undocumented ecosystem. This discovery was a significant outcome of the Coulman High Project's geophysical and environmental fieldwork in 2010-2011 as part of the ANDRILL (ANtarctic geologic DRILLing) program. Edwardsiella andrillae n. sp., lives with most of its column in the <span class="hlt">ice</span> shelf, with only the tentacle crown extending into the <span class="hlt">seawater</span> below. In addition to being the only Antarctic representative of the genus, Edwardsiella andrillae is distinguished from all other species of the genus in the number of tentacles and in the size and distribution of cnidae. The anatomy and histology of Edwardsiella andrillae present no features that explain how this animal withstands the challenges of life in such an unusual habitat.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AMT....10..825D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AMT....10..825D"><span>Simultaneous retrieval of water <span class="hlt">vapour</span>, temperature and cirrus clouds properties from measurements of far infrared spectral radiance over the Antarctic Plateau</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Di Natale, Gianluca; Palchetti, Luca; Bianchini, Giovanni; Del Guasta, Massimo</p> <p>2017-03-01</p> <p>The possibility separating the contributions of the atmospheric state and <span class="hlt">ice</span> clouds by using spectral infrared measurements is a fundamental step to quantifying the cloud effect in climate models. A simultaneous retrieval of cloud and atmospheric parameters from infrared wideband spectra will allow the disentanglement of the spectral interference between these variables. In this paper, we describe the development of a code for the simultaneous retrieval of atmospheric state and <span class="hlt">ice</span> cloud parameters, and its application to the analysis of the spectral measurements acquired by the Radiation Explorer in the Far Infrared - Prototype for Applications and Development (REFIR-PAD) spectroradiometer, which has been in operation at Concordia Station on the Antarctic Plateau since 2012. The code performs the retrieval with a computational time that is comparable with the instrument acquisition time. Water <span class="hlt">vapour</span> and temperature profiles and the cloud optical and microphysical properties, such as the generalised effective diameter and the <span class="hlt">ice</span> water path, are retrieved by exploiting the 230-980 cm-1 spectral band. To simulate atmospheric radiative transfer, the Line-By-Line Radiative Transfer Model (LBLRTM) has been integrated with a specifically developed subroutine based on the δ-Eddington two-stream approximation, whereas the single-scattering properties of cirrus clouds have been derived from a database for hexagonal column habits. In order to detect <span class="hlt">ice</span> clouds, a backscattering and depolarisation lidar, co-located with REFIR-PAD has been used, allowing us to infer the position and the cloud thickness to be used in the retrieval. A climatology of the vertical profiles of water <span class="hlt">vapour</span> and temperature has been performed by using the daily radiosounding available at the station at 12:00 UTC. The climatology has been used to build an a priori profile correlation to constrain the fitting procedure. An optimal estimation method with the Levenberg-Marquardt approach has been</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.A51C3056W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.A51C3056W"><span>Intercomparison of TCCON and MUSICA Water <span class="hlt">Vapour</span> Products</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Weaver, D.; Strong, K.; Deutscher, N. M.; Schneider, M.; Blumenstock, T.; Robinson, J.; Notholt, J.; Sherlock, V.; Griffith, D. W. T.; Barthlott, S.; García, O. E.; Smale, D.; Palm, M.; Jones, N. B.; Hase, F.; Kivi, R.; Ramos, Y. G.; Yoshimura, K.; Sepúlveda, E.; Gómez-Peláez, Á. J.; Gisi, M.; Kohlhepp, R.; Warneke, T.; Dohe, S.; Wiegele, A.; Christner, E.; Lejeune, B.; Demoulin, P.</p> <p>2014-12-01</p> <p>We present an intercomparison between the water <span class="hlt">vapour</span> products from the Total Carbon Column Observing Network (TCCON) and the MUlti-platform remote Sensing of Isotopologues for investigating the Cycle of Atmospheric water (MUSICA), two datasets from ground-based Fourier Transform InfraRed (FTIR) spectrometers with good global representation. Where possible, comparisons to radiosondes are also included. The near-infrared TCCON measurements are optimized to provide precise monitoring of greenhouse gases for carbon cycle studies; however, TCCON's retrievals also produce water <span class="hlt">vapour</span> products. The mid-infrared MUSICA products result from retrievals optimized to give precise and accurate information about H2O, HDO, and δD. The MUSICA water <span class="hlt">vapour</span> products have been validated by extensive intercomparisons with H2O and δD in-situ measurements made from ground, radiosonde, and aircraft (Schneider et al. 2012, 2014), as well as by intercomparisons with satellite-based H2O and δD remote sensing measurements (Wiegele et al., 2014). This dataset provides a valuable reference point for other measurements of water <span class="hlt">vapour</span>. This study is motivated by the limited intercomparisons performed for TCCON water <span class="hlt">vapour</span> products and limited characterisation of their uncertainties. We compare MUSICA and TCCON products to assess the potential for TCCON measurements to contribute to studies of the water cycle, water <span class="hlt">vapour</span>'s role in climate and use as a tracer for atmospheric dynamics, and to evaluate the performance of climate models. The TCCON and MUSICA products result from measurements taken using the same FTIR instruments, enabling a comparison with constant instrumentation. The retrieval techniques differ, however, in their method and a priori information. We assess the impact of these differences and characterize the comparability of the TCCON and MUSICA datasets.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..19.4618H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..19.4618H"><span>Partitioning of <span class="hlt">ice</span> nucleating particles: Which modes matter?</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hande, Luke; Hoose, Corinna</p> <p>2017-04-01</p> <p><span class="hlt">Ice</span> particles in clouds have a large impact on cloud lifetime, precipitation amount, and cloud radiative properties through the indirect aerosol effect. Thus, correctly modelling <span class="hlt">ice</span> formation processes is important for simulations preformed on all spatial and temporal scales. <span class="hlt">Ice</span> forms on aerosol particles through several different mechanisms, namely deposition nucleation, immersion freezing, and contact freezing. However there is conflicting evidence as to which mode dominates, and the relative importance of the three heterogeneous <span class="hlt">ice</span> nucleation mechanisms, as well as homogeneous nucleation, remains an open question. The environmental conditions, and hence the cloud type, have a large impact on determining which nucleation mode dominates. In order to understand this, simulations were performed with the COSMO-LES model, utilising state of the art parameterisations to describe the different nucleation mechanisms for several semi-idealised cloud types commonly occurring over central Europe. The cloud types investigated include a semi-idealised, and an idealised convective cloud, an orographic cloud, and a stratiform cloud. Results show that immersion and contact freezing dominate at warmer temperatures, and under most conditions, deposition nucleation plays only a minor role. In clouds where sufficiently high levels of water <span class="hlt">vapour</span> are present at colder temperatures, deposition nucleation can play a role, however in general homogeneous nucleation dominates at colder temperatures. Since contact nucleation depends on the environmental relative humidity, enhancements in this nucleation mode can be seen in areas of dry air entrainment. The results indicate that <span class="hlt">ice</span> microphysical processes are somewhat sensitve to the environmental conditions and therefore the cloud type.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ACP....16.8125B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ACP....16.8125B"><span>The millennium water <span class="hlt">vapour</span> drop in chemistry-climate model simulations</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Brinkop, Sabine; Dameris, Martin; Jöckel, Patrick; Garny, Hella; Lossow, Stefan; Stiller, Gabriele</p> <p>2016-07-01</p> <p>This study investigates the abrupt and severe water <span class="hlt">vapour</span> decline in the stratosphere beginning in the year 2000 (the "millennium water <span class="hlt">vapour</span> drop") and other similarly strong stratospheric water <span class="hlt">vapour</span> reductions by means of various simulations with the state-of-the-art Chemistry-Climate Model (CCM) EMAC (ECHAM/MESSy Atmospheric Chemistry Model). The model simulations differ with respect to the prescribed sea surface temperatures (SSTs) and whether nudging is applied or not. The CCM EMAC is able to most closely reproduce the signature and pattern of the water <span class="hlt">vapour</span> drop in agreement with those derived from satellite observations if the model is nudged. Model results confirm that this extraordinary water <span class="hlt">vapour</span> decline is particularly obvious in the tropical lower stratosphere and is related to a large decrease in cold point temperature. The drop signal propagates under dilution to the higher stratosphere and to the poles via the Brewer-Dobson circulation (BDC). We found that the driving forces for this significant decline in water <span class="hlt">vapour</span> mixing ratios are tropical sea surface temperature (SST) changes due to a coincidence with a preceding strong El Niño-Southern Oscillation event (1997/1998) followed by a strong La Niña event (1999/2000) and supported by the change of the westerly to the easterly phase of the equatorial stratospheric quasi-biennial oscillation (QBO) in 2000. Correct (observed) SSTs are important for triggering the strong decline in water <span class="hlt">vapour</span>. There are indications that, at least partly, SSTs contribute to the long period of low water <span class="hlt">vapour</span> values from 2001 to 2006. For this period, the specific dynamical state of the atmosphere (overall atmospheric large-scale wind and temperature distribution) is important as well, as it causes the observed persistent low cold point temperatures. These are induced by a period of increased upwelling, which, however, has no corresponding pronounced signature in SSTs anomalies in the tropics. Our free</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26ES..118a2017P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26ES..118a2017P"><span>Investigation of groundwater-<span class="hlt">seawater</span> interactions: a review</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Purwoarminta, A.; Moosdorf, N.; Delinom, R. M.</p> <p>2018-02-01</p> <p>This paper is to review how to investigate the interactions between groundwater and <span class="hlt">seawater</span>. Those interactions divide into two, which are submarine groundwater discharge and <span class="hlt">seawater</span> intrusion. This investigation is important because the interactions can give impact to coastal aquifer and marine ecosystem. On land, fresh groundwater is vulnerable to <span class="hlt">seawater</span> disturbance. Coastal aquifer is under pressure from abstraction caused by population, industry, and agriculture. The pumping can induce <span class="hlt">seawater</span> intrusion and land subsidence. Then in marine, <span class="hlt">seawater</span> mixes with freshwater and it decreases salinity. Low salinity will influence marine ecosystem. The ecosystem will be disturbed by groundwater discharge if that water is contaminated. Based on the argue investigation of groundwater-<span class="hlt">seawater</span> interactions is important and must be accurate because the results are used for coastal water management. To investigate the interactions data, i.e., lithology, pumping tests, hydrochemical data, sea level rise estimates, precipitation data, geophysics, environmental isotopes, and drilling information, should be compiled. The interaction can feed a model to determine how much groundwater extraction happening on coastal areas to prevent <span class="hlt">seawater</span> intrusion and land subsidence. Water resources management on coasts should consider groundwater-<span class="hlt">seawater</span> interactions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24820354','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24820354"><span><span class="hlt">Ice</span> crystallization in ultrafine water-salt aerosols: nucleation, <span class="hlt">ice</span>-solution equilibrium, and internal structure.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hudait, Arpa; Molinero, Valeria</p> <p>2014-06-04</p> <p>Atmospheric aerosols have a strong influence on Earth's climate. Elucidating the physical state and internal structure of atmospheric aqueous aerosols is essential to predict their gas and water uptake, and the locus and rate of atmospherically important heterogeneous reactions. Ultrafine aerosols with sizes between 3 and 15 nm have been detected in large numbers in the troposphere and tropopause. Nanoscopic aerosols arising from bubble bursting of natural and artificial <span class="hlt">seawater</span> have been identified in laboratory and field experiments. The internal structure and phase state of these aerosols, however, cannot yet be determined in experiments. Here we use molecular simulations to investigate the phase behavior and internal structure of liquid, vitrified, and crystallized water-salt ultrafine aerosols with radii from 2.5 to 9.5 nm and with up to 10% moles of ions. We find that both <span class="hlt">ice</span> crystallization and vitrification of the nanodroplets lead to demixing of pure water from the solutions. Vitrification of aqueous nanodroplets yields nanodomains of pure low-density amorphous <span class="hlt">ice</span> in coexistence with vitrified solute rich aqueous glass. The melting temperature of <span class="hlt">ice</span> in the aerosols decreases monotonically with an increase of solute fraction and decrease of radius. The simulations reveal that nucleation of <span class="hlt">ice</span> occurs homogeneously at the subsurface of the water-salt nanoparticles. Subsequent <span class="hlt">ice</span> growth yields phase-segregated, internally mixed, aerosols with two phases in equilibrium: a concentrated water-salt amorphous mixture and a spherical cap-like <span class="hlt">ice</span> nanophase. The surface of the crystallized aerosols is heterogeneous, with <span class="hlt">ice</span> and solution exposed to the vapor. Free energy calculations indicate that as the concentration of salt in the particles, the advance of the crystallization, or the size of the particles increase, the stability of the spherical cap structure increases with respect to the alternative structure in which a core of <span class="hlt">ice</span> is fully surrounded by</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24599176','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24599176"><span>Structure and sublimation of water <span class="hlt">ice</span> films grown in vacuo at 120-190 K studied by positron and positronium annihilation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Townrow, S; Coleman, P G</p> <p>2014-03-26</p> <p>The crystalline structure of ∼ 5-20 μm water <span class="hlt">ice</span> films grown at 165 and 172 K has been probed by measuring the fraction of positrons forming ortho-positronium (ortho-Ps) and decaying into three gamma photons. It has been established that films grown at slower rates (water <span class="hlt">vapour</span> pressure ≥ 1 mPa) have lower concentrations of lattice defects and closed pores, which act as Ps traps, than those grown at higher rates (<span class="hlt">vapour</span> pressure ∼ 100 mPa), evidenced by ortho-Ps diffusion lengths being approximately four times greater in the former. By varying the growth temperature between 162 and 182 K it was found that films become less disordered at temperatures above ∼ 172 K, with the ortho-Ps diffusion length rising by ∼ 60%, in this range. The sublimation energy for water <span class="hlt">ice</span> films grown on copper has been measured to be 0.462(5) eV using the time dependence of positron annihilation parameters from 165 to 195 K, in agreement with earlier studies and with no measurable dependence on growth rate and thermal history.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=20030071639&hterms=water+scarcity&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3Dwater%2Bscarcity','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=20030071639&hterms=water+scarcity&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D50%26Ntt%3Dwater%2Bscarcity"><span>Rootless Cones on Mars: A Consequence of Lava-Ground <span class="hlt">Ice</span> Interaction</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Fagents, S. A.; Greeley, R.; Lanagan, P.</p> <p>2002-01-01</p> <p>Fields of small cratered cones on Mars are interpreted to have formed by rootless eruptions due to explosive interaction of lava with ground <span class="hlt">ice</span> contained within the regolith beneath the flow. Melting and vaporization of the <span class="hlt">ice</span>, and subsequent explosive expansion of the <span class="hlt">vapour</span>, act to excavate the lava and construct a rootless cone around the explosion site. Similar features are found in Iceland, where flowing lava encountered water-saturated substrates. The martian cones have basal diameters of c. 30-1000 m and are located predominantly in the northern volcanic plains. High-resolution Mars Orbiter Camera images offer significant improvements over Viking data for interpretation of cone origins. A new model of the dynamics of cone formation indicates that very modest amounts of water <span class="hlt">ice</span> are required to initiate and sustain the explosive interactions that produced the observed features. This is consistent with the likely low availability of water <span class="hlt">ice</span> in the martian regolith. The scarcity of impact craters on many of the host lava flows indicates very young ages, suggesting that ground <span class="hlt">ice</span> was present as recently as less than 10 - l00 Ma, and may persist today. Rootless cones therefore act as a spatial and temporal probe of the distribution of ground <span class="hlt">ice</span> on Mars, which is of key significance in understanding the evolution of the martian climate. The location of water in liquid or solid form is of great importance to future robotic and human exploration strategies, and to the search for extraterrestrial life.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/15137762','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/15137762"><span>Ultrastructure in frozen/etched saline solutions: on the internal cleansing of <span class="hlt">ice</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Menger, Fredric M; Galloway, Ashley L; Chlebowski, Mary E; Apkarian, Robert P</p> <p>2004-05-19</p> <p><span class="hlt">Seawater</span>, with its 3.5% salt content, freezes into hexagonal <span class="hlt">ice</span> (Ih) that encloses concentrated brine within its matrix. When unsubmerged sea <span class="hlt">ice</span> reaches a certain height and temperature, the brine drains downward through narrow channels. This mechanism was now modeled by frozen 2-3.5% saline as investigated by cryo-etch high-resolution secondary electron microscopy. Thus, saline was either plunge-frozen in liquid ethane at -183 degrees C or else high-pressure frozen to -105 degrees C in 5-6 ms. <span class="hlt">Ice</span> from a freshly exposed surface was then subjected to a high-vacuum sublimation ("etching"), a procedure that removes pure bulk <span class="hlt">ice</span> in preference to <span class="hlt">ice</span> from frozen hydrated salt. After chromium-coating the etched surface with a 2-nm film, the sample was examined by cryo-HRSEM. Granular icy "fences" were seen surrounding empty areas where amorphous <span class="hlt">ice</span> had originally resided. Since the fences, about 1-2 mum high, survived the etching, it is likely that they consist of frozen brine. The presence of such fences suggests that, during freezing, saline can purge itself of salt with remarkable speed (5-6 ms). Alternatively, channels (perhaps routed around submicroscopic crystallites of cubic <span class="hlt">ice</span> (Ic) embedded in the amorphous <span class="hlt">ice</span> at -105 degrees C) can guide the migration of salt to the periphery of <span class="hlt">ice</span> patches. Macromolecules fail to form fences because they diffuse too slowly or because they are too large to pass through the channels.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012GGG....1310014S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012GGG....1310014S"><span>Cenozoic <span class="hlt">seawater</span> Sr/Ca evolution</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sosdian, Sindia M.; Lear, Caroline H.; Tao, Kai; Grossman, Ethan L.; O'Dea, Aaron; Rosenthal, Yair</p> <p>2012-10-01</p> <p>Records of <span class="hlt">seawater</span> chemistry help constrain temporal variations in geochemical processes that impact the global carbon cycle and climate through Earth's history. Here we reconstruct Cenozoic <span class="hlt">seawater</span> Sr/Ca (Sr/Casw) using fossil Conus and turritellid gastropod Sr/Ca. Combined with an oxygen isotope paleotemperature record from the same samples, the gastropod record suggests that Sr/Caswwas slightly higher in the Eocene (˜11.4 ± 3 mmol/mol) than today (˜8.54 mmol/mol) and remained relatively stable from the mid- to late Cenozoic. We compare our gastropod Cenozoic Sr/Casw record with a published turritellid gastropod Sr/Casw record and other published biogenic (benthic foraminifera, fossil fish teeth) and inorganic precipitate (calcite veins) Sr/Caswrecords. Once the uncertainties with our gastropod-derived Sr/Casw are taken into account the Sr/Casw record agrees reasonably well with biogenic Sr/Caswrecords. Assuming a <span class="hlt">seawater</span> [Ca] history derived from marine evaporite inclusions, all biogenic-based Sr/Casw reconstructions imply decreasing <span class="hlt">seawater</span> [Sr] through the Cenozoic, whereas the calcite vein Sr/Casw reconstruction implies increasing [Sr] through the Cenozoic. We apply a simple geochemical model to examine the implications of divergence among these <span class="hlt">seawater</span> [Sr] reconstructions and suggest that the interpretation and uncertainties associated with the gastropod and calcite vein proxies need to be revisited. Used in conjunction with records of carbonate depositional fluxes, our favored <span class="hlt">seawater</span> Sr/Ca scenarios point to a significant increase in the proportion of aragonite versus calcite deposition in shelf sediments from the Middle Miocene, coincident with the proliferation of coral reefs. We propose that this occurred at least 10 million years after the <span class="hlt">seawater</span> Mg/Ca threshold was passed, and was instead aided by declining levels of atmospheric carbon dioxide.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..19.6235R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..19.6235R"><span>Strontium (Sr) separation from <span class="hlt">seawater</span> using titanate adsorbents: Effects of <span class="hlt">seawater</span> matrix ions on Sr sorption behavior</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ryu, Jungho; Hong, Hye-jin; Ryu, Taegong; Park, In-Su</p> <p>2017-04-01</p> <p>Strontium (Sr) which has many industrial applications such as ferrite magnet, ceramic, and fire works exists in <span class="hlt">seawater</span> with the concentration of approximately 7 mg/L. In previous report estimating economic potential on recovery of various elements from <span class="hlt">seawater</span> in terms of their commercial values and concentrations in <span class="hlt">seawater</span>, Sr locates upper than approximate break-even line, which implies Sr recovery from <span class="hlt">seawater</span> can be potentially profitable. Recently, Sr separation from <span class="hlt">seawater</span> has received great attention in the environmental aspect after Fukushima Nuclear Power Plant (NPP) accident which released much amount of radioactive Sr and Cs. Accordingly, the efficient separation of radioactive elements released to <span class="hlt">seawater</span> has become critical as an important technological need as well as their removal from radioactive wastes. So far, it has been introduced to separate Sr from aqueous media by various methods including solvent extraction, adsorption by solid materials, and ion exchange. Among them, the adsorption technique using solid adsorbents is of great interest for selectively separating Sr from <span class="hlt">seawater</span> with respect to low concentration level of Sr. In this study, we synthesized titanate nanotube (TiNT) by simple hydrothermal reaction, characterized its physicochemical properties, and systematically evaluated Sr sorption behavior under various reaction conditions corresponding to <span class="hlt">seawater</span> environment. The synthesized TiNT exhibited the fibril-type nanotube structure with high specific surface area of 260 m2/g. The adsorption of Sr on TiNT rapidly occurred following pseudo-second-order kinetic model, and was in good agreement with Langmuir isotherm model, indicating maximum adsorption capacity of 97 mg/g. Based on Sr uptake and Na release with stoichiometric balance, sorption mechanism of Sr on TiNT was found to be ion-exchange between Na in TiNT lattice and Sr in solution phase, which was also confirmed by XRD and Raman analysis. Among competitive ions, Ca</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1337148-rechargeable-seawater-battery-its-electrochemical-mechanism','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1337148-rechargeable-seawater-battery-its-electrochemical-mechanism"><span>Rechargeable <span class="hlt">Seawater</span> Battery and Its Electrochemical Mechanism</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Kim, Jae-Kwang; Lee, Eungje; Kim, Hyojin; ...</p> <p>2014-11-25</p> <p>Here in this paper, we explore the electrochemical mechanism of a novel rechargeable <span class="hlt">seawater</span> battery system that uses <span class="hlt">seawater</span> as the cathode material. Sodium is harvested from <span class="hlt">seawater</span> while charging the battery, and the harvested sodium is discharged with oxygen dissolved in the <span class="hlt">seawater</span>, functioning as oxidants to produce electricity. The <span class="hlt">seawater</span> provides both anode (Na metal) and cathode (O 2) materials for the proposed battery. Based on the discharge voltage (~2.9 V) with participation of O 2 and the charge voltage (~4.1 V) with Cl 2 evolution during the first cycle, a voltage efficiency of about 73% is obtained.more » If the <span class="hlt">seawater</span> battery is constructed using hard carbon as the anode and a Na super ion conductor as the solid electrolyte, a strong cycle performance of 84% is observed after 40 cycles.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.C23B0788M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.C23B0788M"><span>Arctic Sea <span class="hlt">Ice</span> Basal Melt Onset Variability and Associated Ocean Surface Heating</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Merrick, R. A.; Hutchings, J. K.</p> <p>2015-12-01</p> <p>The interannual and regional variability in Arctic sea <span class="hlt">ice</span> melt has previously been characterized only in terms of surface melting. A focus on the variability in the onset of basal melt is additionally required to understand Arctic melt patterns. Monitoring basal melt provides a glimpse into the importance of ocean heating to sea <span class="hlt">ice</span> melt. This warming is predominantly through <span class="hlt">seawater</span> exposure due to lead opening and the associated solar warming at the ocean's surface. We present the temporal variability in basal melt onset observed by <span class="hlt">ice</span> mass balance buoys throughout the Arctic Ocean since 2003, providing a different perspective than the satellite microwave data used to measure the onset of surface melt. We found that melt onset varies greatly, even for buoys deployed within 100km of each other. Therefore large volumes of data are necessary to accurately estimate the variability of basal melt onset. Once the variability of basal melt onset has been identified, we can investigate how this range has been changing as a response to atmospheric and oceanic warming, changes in <span class="hlt">ice</span> morphology as well as the intensification of the <span class="hlt">ice</span> albedo feedback.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1349435','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1349435"><span>A water activity based model of heterogeneous <span class="hlt">ice</span> nucleation kinetics for freezing of water and aqueous solution droplets</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Knopf, Daniel A.; Alpert, Peter A.</p> <p></p> <p>Immersion freezing of water and aqueous solutions by particles acting as <span class="hlt">ice</span> nuclei (IN) is a common process of heterogeneous <span class="hlt">ice</span> nucleation which occurs in many environments, especially in the atmosphere where it results in the glaciation of clouds. Here we experimentally show, using a variety of IN types suspended in various aqueous solutions, that immersion freezing temperatures and kinetics can be described solely by temperature, T, and solution water activity, aw, which is the ratio of the <span class="hlt">vapour</span> pressure of the solution and the saturation water <span class="hlt">vapour</span> pressure under the same conditions and, in equilibrium, equivalent to relative humiditymore » (RH). This allows the freezing point and corresponding heterogeneous <span class="hlt">ice</span> nucleation rate coefficient, Jhet, to be uniquely expressed by T and aw, a result we term the aw based immersion freezing model (ABIFM). This method is independent of the nature of the solute and accounts for several varying parameters, including cooling rate and IN surface area, while providing a holistic description of immersion freezing and allowing prediction of freezing temperatures, Jhet, frozen fractions, <span class="hlt">ice</span> particle production rates and numbers. Our findings are based on experimental freezing data collected for various IN surface areas, A, and cooling rates, r, of droplets variously containing marine biogenic material, two soil humic acids, four mineral dusts, and one organic monolayer acting as IN. For all investigated IN types we demonstrate that droplet freezing temperatures increase as A increases. Similarly, droplet freezing temperatures increase as the cooling rate decreases. The log 10(J het) values for the various IN types derived exclusively by T and aw, provide a complete description of the heterogeneous <span class="hlt">ice</span> nucleation kinetics. Thus, the ABIFM can be applied over the entire range of T, RH, total particulate surface area, and cloud activation timescales typical of atmospheric conditions. Finally, we demonstrate that ABIFM can</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_5");'>5</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li class="active"><span>7</span></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_7 --> <div id="page_8" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li class="active"><span>8</span></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="141"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24601020','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24601020"><span>A water activity based model of heterogeneous <span class="hlt">ice</span> nucleation kinetics for freezing of water and aqueous solution droplets.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Knopf, Daniel A; Alpert, Peter A</p> <p>2013-01-01</p> <p>Immersion freezing of water and aqueous solutions by particles acting as <span class="hlt">ice</span> nuclei (IN) is a common process of heterogeneous <span class="hlt">ice</span> nucleation which occurs in many environments, especially in the atmosphere where it results in the glaciation of clouds. Here we experimentally show, using a variety of IN types suspended in various aqueous solutions, that immersion freezing temperatures and kinetics can be described solely by temperature, T, and solution water activity, a(w), which is the ratio of the <span class="hlt">vapour</span> pressure of the solution and the saturation water <span class="hlt">vapour</span> pressure under the same conditions and, in equilibrium, equivalent to relative humidity (RH). This allows the freezing point and corresponding heterogeneous <span class="hlt">ice</span> nucleation rate coefficient, J(het), to be uniquely expressed by T and a(w), a result we term the a(w) based immersion freezing model (ABIFM). This method is independent of the nature of the solute and accounts for several varying parameters, including cooling rate and IN surface area, while providing a holistic description of immersion freezing and allowing prediction of freezing temperatures, J(het), frozen fractions, <span class="hlt">ice</span> particle production rates and numbers. Our findings are based on experimental freezing data collected for various IN surface areas, A, and cooling rates, r, of droplets variously containing marine biogenic material, two soil humic acids, four mineral dusts, and one organic monolayer acting as IN. For all investigated IN types we demonstrate that droplet freezing temperatures increase as A increases. Similarly, droplet freezing temperatures increase as the cooling rate decreases. The log10(J(het)) values for the various IN types derived exclusively by Tand a(w), provide a complete description of the heterogeneous <span class="hlt">ice</span> nucleation kinetics. Thus, the ABIFM can be applied over the entire range of T, RH, total particulate surface area, and cloud activation timescales typical of atmospheric conditions. Lastly, we demonstrate that ABIFM can</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1349435-water-activity-based-model-heterogeneous-ice-nucleation-kinetics-freezing-water-aqueous-solution-droplets','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1349435-water-activity-based-model-heterogeneous-ice-nucleation-kinetics-freezing-water-aqueous-solution-droplets"><span>A water activity based model of heterogeneous <span class="hlt">ice</span> nucleation kinetics for freezing of water and aqueous solution droplets</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Knopf, Daniel A.; Alpert, Peter A.</p> <p>2013-04-24</p> <p>Immersion freezing of water and aqueous solutions by particles acting as <span class="hlt">ice</span> nuclei (IN) is a common process of heterogeneous <span class="hlt">ice</span> nucleation which occurs in many environments, especially in the atmosphere where it results in the glaciation of clouds. Here we experimentally show, using a variety of IN types suspended in various aqueous solutions, that immersion freezing temperatures and kinetics can be described solely by temperature, T, and solution water activity, aw, which is the ratio of the <span class="hlt">vapour</span> pressure of the solution and the saturation water <span class="hlt">vapour</span> pressure under the same conditions and, in equilibrium, equivalent to relative humiditymore » (RH). This allows the freezing point and corresponding heterogeneous <span class="hlt">ice</span> nucleation rate coefficient, Jhet, to be uniquely expressed by T and aw, a result we term the aw based immersion freezing model (ABIFM). This method is independent of the nature of the solute and accounts for several varying parameters, including cooling rate and IN surface area, while providing a holistic description of immersion freezing and allowing prediction of freezing temperatures, Jhet, frozen fractions, <span class="hlt">ice</span> particle production rates and numbers. Our findings are based on experimental freezing data collected for various IN surface areas, A, and cooling rates, r, of droplets variously containing marine biogenic material, two soil humic acids, four mineral dusts, and one organic monolayer acting as IN. For all investigated IN types we demonstrate that droplet freezing temperatures increase as A increases. Similarly, droplet freezing temperatures increase as the cooling rate decreases. The log 10(J het) values for the various IN types derived exclusively by T and aw, provide a complete description of the heterogeneous <span class="hlt">ice</span> nucleation kinetics. Thus, the ABIFM can be applied over the entire range of T, RH, total particulate surface area, and cloud activation timescales typical of atmospheric conditions. Finally, we demonstrate that ABIFM can</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.P34A..04B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.P34A..04B"><span>Slush Fund: Modeling the Multiphase Physics of Oceanic <span class="hlt">Ices</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Buffo, J.; Schmidt, B. E.</p> <p>2016-12-01</p> <p>The prevalence of <span class="hlt">ice</span> interacting with an ocean, both on Earth and throughout the solar system, and its crucial role as the mediator of exchange between the hydrosphere below and atmosphere above, have made quantifying the thermodynamic, chemical, and physical properties of the <span class="hlt">ice</span> highly desirable. While direct observations of these quantities exist, their scarcity increases with the difficulty of obtainment; the basal surfaces of terrestrial <span class="hlt">ice</span> shelves remain largely unexplored and the icy interiors of moons like Europa and Enceladus have never been directly observed. Our understanding of these entities thus relies on numerical simulation, and the efficacy of their incorporation into larger systems models is dependent on the accuracy of these initial simulations. One characteristic of <span class="hlt">seawater</span>, likely shared by the oceans of icy moons, is that it is a solution. As such, when it is frozen a majority of the solute is rejected from the forming <span class="hlt">ice</span>, concentrating in interstitial pockets and channels, producing a two-component reactive porous media known as a mushy layer. The multiphase nature of this layer affects the evolution and dynamics of the overlying <span class="hlt">ice</span> mass. Additionally <span class="hlt">ice</span> can form in the water column and accrete onto the basal surface of these <span class="hlt">ice</span> masses via buoyancy driven sedimentation as frazil or platelet <span class="hlt">ice</span>. Numerical models hoping to accurately represent <span class="hlt">ice</span>-ocean interactions should include the multiphase behavior of these two phenomena. While models of sea <span class="hlt">ice</span> have begun to incorporate multiphase physics into their capabilities, no models of <span class="hlt">ice</span> shelves/shells explicitly account for the two-phase behavior of the <span class="hlt">ice</span>-ocean interface. Here we present a 1D multiphase model of floating oceanic <span class="hlt">ice</span> that includes parameterizations of both density driven advection within the `mushy layer' and buoyancy driven sedimentation. The model is validated against contemporary sea <span class="hlt">ice</span> models and observational data. Environmental stresses such as supercooling and</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3859642','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3859642"><span>Edwardsiella andrillae, a New Species of Sea Anemone from Antarctic <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Daly, Marymegan; Rack, Frank; Zook, Robert</p> <p>2013-01-01</p> <p>Exploration of the lower surface of the Ross <span class="hlt">Ice</span> Shelf in Antarctica by the Submersible Capable of under-<span class="hlt">Ice</span> Navigation and Imaging (SCINI) remotely operated vehicle discovered a new species of sea anemone living in this previously undocumented ecosystem. This discovery was a significant outcome of the Coulman High Project’s geophysical and environmental fieldwork in 2010-2011 as part of the ANDRILL (ANtarctic geologic DRILLing) program. Edwardsiella andrillae n. sp., lives with most of its column in the <span class="hlt">ice</span> shelf, with only the tentacle crown extending into the <span class="hlt">seawater</span> below. In addition to being the only Antarctic representative of the genus, Edwardsiella andrillae is distinguished from all other species of the genus in the number of tentacles and in the size and distribution of cnidae. The anatomy and histology of Edwardsiella andrillae present no features that explain how this animal withstands the challenges of life in such an unusual habitat. PMID:24349517</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28414981','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28414981"><span>Claims in <span class="hlt">vapour</span> device (e-cigarette) regulation: A Narrative Policy Framework analysis.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>O'Leary, Renée; Borland, Ron; Stockwell, Tim; MacDonald, Marjorie</p> <p>2017-06-01</p> <p>The electronic cigarette or e-cigarette (<span class="hlt">vapour</span> device) is a consumer product undergoing rapid growth, and governments have been adopting regulations on the sale of the devices and their nicotine liquids. Competing claims about <span class="hlt">vapour</span> devices have ignited a contentious debate in the public health community. What claims have been taken up in the state arena, and how have they possibly influenced regulatory outcomes? This study utilized Narrative Policy Framework to analyze the claims made about <span class="hlt">vapour</span> devices in legislation recommendation reports from Queensland Australia, Canada, and the European Union, and the 2016 deeming rule legislation from the United States, and examined the claims and the regulatory outcomes in these jurisdictions. The vast majority of claims in the policy documents represented <span class="hlt">vapour</span> devices as a threat: an unsafe product harming the health of <span class="hlt">vapour</span> device users, a gateway product promoting youth tobacco uptake, and a quasi-tobacco product impeding tobacco control. The opportunity for <span class="hlt">vapour</span> devices to promote cessation or reduce exposure to toxins was very rarely presented, and these positive claims were not discussed at all in two of the four documents studied. The dominant claims of <span class="hlt">vapour</span> devices as a public health threat have supported regulations that have limited their potential as a harm reduction strategy. Future policy debates should evaluate the opportunities for <span class="hlt">vapour</span> devices to decrease the health and social burdens of the tobacco epidemic. Copyright © 2017 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25933565','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25933565"><span>Atrial and ventricular septal changes in ethanol <span class="hlt">vapour</span> exposed chick embryos.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kamran, Kiran; Khan, Muhammad Yunus; Minhas, Liaqat Ali</p> <p>2015-03-01</p> <p>To study the effects of ethanol <span class="hlt">vapour</span> exposure on development of atrial and ventricular septa of chick embryo. The experimental study was conducted at the College of Physicians and Surgeons, Islamabad, from 2006 to 2007. The experimental and control groups were further divided into three subgroups based on the day of sacrifice. The experimental group was exposed to ethanol <span class="hlt">vapours</span> produced in a specially-designed <span class="hlt">vapour</span> chamber and then compared with age-matched controls. There were 90 eggs in each of the two groups. The development of inter-ventricular septum completed at day 7 of development in chick embryo. Ethanol <span class="hlt">vapour</span> exposure produced a small discontinuity at day 10 of development in a chick embryo which may be labelled as ventricular septal defect since ventricular development is completed by day 7. Interatrial septum formed till day 7 with small perforations which persisted till hatching. Ethanol <span class="hlt">vapour</span> exposure may lead to ventricular septal defect.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70174110','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70174110"><span>Freshwater to <span class="hlt">seawater</span> transitions in migratory fishes</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Zydlewski, Joseph D.; Michael P. Wilkie,</p> <p>2012-01-01</p> <p>The transition from freshwater to <span class="hlt">seawater</span> is integral to the life history of many fishes. Diverse migratory fishes express anadromous, catadromous, and amphidromous life histories, while others make incomplete transits between freshwater and <span class="hlt">seawater</span>. The physiological mechanisms of osmoregulation are widely conserved among phylogenetically diverse species. Diadromous fishes moving between freshwater and <span class="hlt">seawater</span> develop osmoregulatory mechanisms for different environmental salinities. Freshwater to <span class="hlt">seawater</span> transition involves hormonally mediated changes in gill ionocytes and the transport proteins associated with hypoosmoregulation, increased <span class="hlt">seawater</span> ingestion and water absorption in the intestine, and reduced urinary water losses. Fishes attain salinity tolerance through early development, gradual acclimation, or environmentally or developmentally cued adaptations. This chapter describes adaptations in diverse taxa and the effects of salinity on growth. Identifying common strategies in diadromous fishes moving between freshwater and <span class="hlt">seawater</span> will reveal the ecological and physiological basis for maintaining homeostasis in different salinities, and inform efforts to conserve and manage migratory euryhaline fishes.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.C13D..08T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.C13D..08T"><span>Grounding Zones, Subglacial Lakes, and Dynamics of an Antarctic <span class="hlt">Ice</span> Stream: The WISSARD Glaciological Experiment</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Tulaczyk, S. M.; Schwartz, S. Y.; Fisher, A. T.; Powell, R. D.; Fricker, H. A.; Anandakrishnan, S.; Horgan, H. J.; Scherer, R. P.; Walter, J. I.; Siegfried, M. R.; Mikucki, J.; Christianson, K.; Beem, L.; Mankoff, K. D.; Carter, S. P.; Hodson, T. O.; Marsh, O.; Barcheck, C. G.; Branecky, C.; Neuhaus, S.; Jacobel, R. W.</p> <p>2015-12-01</p> <p>Interactions of West Antarctic <span class="hlt">ice</span> streams with meltwater at their beds, and with <span class="hlt">seawater</span> at their grounding lines, are widely considered to be the primary drivers of <span class="hlt">ice</span> stream flow variability on different timescales. Understanding of processes controlling <span class="hlt">ice</span> flow variability is needed to build quantitative models of the Antarctic <span class="hlt">Ice</span> Sheet that can be used to help predict its future behavior and to reconstruct its past evolution. The <span class="hlt">ice</span> plain of Whillans <span class="hlt">Ice</span> Stream provides a natural glaciological laboratory for investigations of Antarctic <span class="hlt">ice</span> flow dynamics because of its highly variable flow rate modulated by tidal processes and fill-drain cycles of subglacial lakes. Moreover, this part of Antarctica has one of the longest time series of glaciological observations, which can be used to put recently acquired datasets in a multi-decadal context. Since 2007 Whillans <span class="hlt">Ice</span> Stream has been the focus of a regional glaciological experiment, which included surface GPS and passive-source seismic sensors, radar and seismic imaging of subglacial properties, as well as deep borehole geophysical sensors. This experiment was possible thanks to the NSF-funded multidisciplinary WISSARD project (Whillans <span class="hlt">Ice</span> Stream Subglacial Access Research Drilling). Here we will review the datasets collected during the WISSARD glaciological experiment and report on selected results pertaining to interactions of this <span class="hlt">ice</span> stream with water at its bed and its grounding line.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AIPC.1728b0290R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AIPC.1728b0290R"><span>Sensing response of copper phthalocyanine salt dispersed glass with organic <span class="hlt">vapours</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ridhi, R.; Sachdeva, Sheenam; Saini, G. S. S.; Tripathi, S. K.</p> <p>2016-05-01</p> <p>Copper Phthalocyanine and other Metal Phthalocyanines are very flexible and tuned easily to modify their structural, spectroscopic, optical and electrical properties by either functionalizing them with various substituent groups or by replacing or adding a ligand to the central metal atom in the phthalocyanine ring and accordingly can be made sensitive and selective to various organic species or gaseous <span class="hlt">vapours</span>. In the present work, we have dispersed Copper Phthalocyanine Salt (CuPcS) in sol-gel glass form using chemical route sol-gel method and studied its sensing mechanism with organic <span class="hlt">vapours</span> like methanol and benzene and found that current increases onto their exposure with <span class="hlt">vapours</span>. A variation in the activation energies was also observed with exposure of <span class="hlt">vapours</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004MeScT..15.1285L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004MeScT..15.1285L"><span>Diode laser-induced infrared fluorescence of water <span class="hlt">vapour</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Li, Hejie; Hanson, Ronald K.; Jeffries, Jay B.</p> <p>2004-07-01</p> <p>Infrared laser-induced fluorescence (LIF) of water <span class="hlt">vapour</span> was investigated for its potential as a spatially resolved gasdynamic diagnostic. A cw diode laser operating near 1392 nm was scanned across a single absorption transition in the ngr1 + ngr3 band of H2O in a static cell, and the resulting fluorescence signal was collected near 2.7 µm (both ngr1 and ngr3 bands). Experiments were conducted at low pressure in pure water <span class="hlt">vapour</span> and mixtures of water <span class="hlt">vapour</span> and N2 using a 20 mW laser in a double-pass arrangement. A simple analytical model was developed to relate LIF intensity to gas properties as a function of laser power. The spectrally resolved, single-line excitation spectrum was fitted with a Voigt profile, allowing inference of the water <span class="hlt">vapour</span> temperature from the Doppler-broadened component of the measured fluorescence lineshape. A two-line excitation scheme was also investigated as a means of measuring temperature with reduced measurement time. From these initial measurements, we estimate that a practical sensor for atmospheric pressure applications would require a minimum of 1-2 W of laser power for two-line, fixed-wavelength temperature measurements and a minimum of about 70 W of power for scanned-wavelength measurements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20020004188','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20020004188"><span>Modeling South Pacific <span class="hlt">Ice</span>-Ocean Interactions in the Global Climate System</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Holland, David M.; Jenkins, Adrian; Jacobs, Stanley S.</p> <p>2001-01-01</p> <p>The objective of this project has been to improve the modeling of interactions between large Antarctic <span class="hlt">ice</span> shelves and adjacent regions of the Southern Ocean. Our larger goal is to gain a better understanding of the extent to which the ocean controls <span class="hlt">ice</span> shelf attrition, thereby influencing the size and dynamics of the Antarctic <span class="hlt">Ice</span> Sheet. Melting and freezing under <span class="hlt">ice</span> shelves also impacts <span class="hlt">seawater</span> properties, regional upwelling and sinking and the larger-scale ocean circulation. Modifying an isopycnal coordinate general circulation model for use in sub-<span class="hlt">ice</span> shelf cavities, we found that the abrupt change in water column thickness at an <span class="hlt">ice</span> shelf front does not form a strong barrier to buoyancy-driven circulation across the front. Outflow along the <span class="hlt">ice</span> shelf base, driven by melting of the thickest <span class="hlt">ice</span>, is balanced by deep inflow. Substantial effort was focused on the Filchner-Ronne cavity, where other models have been applied and time-series records are available from instruments suspended beneath the <span class="hlt">ice</span>. A model comparison indicated that observed changes in the production of High Salinity Shelf Water could have a major impact on circulation within the cavity. This water propagates into the cavity with an asymmetric seasonal signal that has similar phasing and shape in the model and observations, and can be related to winter production at the sea surface. Even remote parts of the sub-<span class="hlt">ice</span> shelf cavity are impacted by external forcing on sub-annual time scales. This shows that cavity circulations and products, and therefore cavity shape, will respond to interannual variability in sea <span class="hlt">ice</span> production and longer-term climate change. The isopycnal model gives generally lower net melt rates than have been obtained from other models and oceanographic data, perhaps due to its boundary layer formulation, or the lack of tidal forcing. Work continues on a manuscript describing the Ross cavity results.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1159457','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1159457"><span>Rapid determination of actinides in <span class="hlt">seawater</span> samples</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Maxwell, Sherrod L.; Culligan, Brian K.; Hutchison, Jay B.</p> <p>2014-03-09</p> <p>A new rapid method for the determination of actinides in <span class="hlt">seawater</span> samples has been developed at the Savannah River National Laboratory. The actinides can be measured by alpha spectrometry or inductively-coupled plasma mass spectrometry. The new method employs novel pre-concentration steps to collect the actinide isotopes quickly from 80 L or more of <span class="hlt">seawater</span>. Actinides are co-precipitated using an iron hydroxide co-precipitation step enhanced with Ti +3 reductant, followed by lanthanum fluoride co-precipitation. Stacked TEVA Resin and TRU Resin cartridges are used to rapidly separate Pu, U, and Np isotopes from <span class="hlt">seawater</span> samples. TEVA Resin and DGA Resin were usedmore » to separate and measure Pu, Am and Cm isotopes in <span class="hlt">seawater</span> volumes up to 80 L. This robust method is ideal for emergency <span class="hlt">seawater</span> samples following a radiological incident. It can also be used, however, for the routine analysis of <span class="hlt">seawater</span> samples for oceanographic studies to enhance efficiency and productivity. In contrast, many current methods to determine actinides in <span class="hlt">seawater</span> can take 1–2 weeks and provide chemical yields of ~30–60 %. This new sample preparation method can be performed in 4–8 h with tracer yields of ~85–95 %. By employing a rapid, robust sample preparation method with high chemical yields, less <span class="hlt">seawater</span> is needed to achieve lower or comparable detection limits for actinide isotopes with less time and effort.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1255257-co2-fluxing-collapses-metal-mobility-magmatic-vapour','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1255257-co2-fluxing-collapses-metal-mobility-magmatic-vapour"><span>CO 2-fluxing collapses metal mobility in magmatic <span class="hlt">vapour</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>van Hinsberg, V. J.; Berlo, K.; Migdisov, A. A.; ...</p> <p>2016-05-18</p> <p>Magmatic systems host many types of ore deposits, including world-class deposits of copper and gold. Magmas are commonly an important source of metals and ore-forming fluids in these systems. In many magmatic-hydrothermal systems, low-density aqueous fluids, or <span class="hlt">vapours</span>, are significant metal carriers. Such <span class="hlt">vapours</span> are water-dominated shallowly, but fluxing of CO 2-rich <span class="hlt">vapour</span> exsolved from deeper magma is now recognised as ubiquitous during open-system magma degassing. Furthermore, we show that such CO 2-fluxing leads to a sharp drop in element solubility, up to a factor of 10,000 for Cu, and thereby provides a highly efficient, but as yet unrecognised mechanismmore » for metal deposition.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012AGUFMPP33B2117R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012AGUFMPP33B2117R"><span>Paleogene <span class="hlt">Seawater</span> Osmium Isotope Records</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rolewicz, Z.; Thomas, D. J.; Marcantonio, F.</p> <p>2012-12-01</p> <p>Paleoceanographic reconstructions of the Late Cretaceous and early Cenozoic require enhanced geographic coverage, particularly in the Pacific, in order to better constrain meridional variations in environmental conditions. The challenge with the existing inventory of Pacific deep-sea cores is that they consist almost exclusively of pelagic clay with little existing age control. Pelagic clay sequences are useful for reconstructions of dust accumulation and water mass composition, but accurate correlation of these records to other sites requires improved age control. Recent work indicates that <span class="hlt">seawater</span> Os isotope analyses provide useful age control for red clay sequences. The residence time of Os in <span class="hlt">seawater</span> is relatively long compared to oceanic mixing, therefore the global <span class="hlt">seawater</span> 187Os/188Os composition is practically homogeneous. A growing body of Late Cretaceous and Cenozoic data has constrained the evolution of the <span class="hlt">seawater</span> Os isotopic composition and this curve is now a viable stratigraphic tool, employed in dating layers of Fe-Mn crusts (e.g., Klemm et al., 2005). Ravizza (2007) also demonstrated that the <span class="hlt">seawater</span> Os isotopic composition can be extracted reliably from pelagic red clay sediments by analyzing the leached oxide minerals. The drawback to using <span class="hlt">seawater</span> Os isotope stratigraphy to date Paleogene age sediments is that the compilation of existing data has some significant temporal gaps, notably between ~38 and 55 Ma. To improve the temporal resolution of the <span class="hlt">seawater</span> Os isotope curve, we present new data from Ocean Drilling Program (ODP) Site 865 in the equatorial Pacific. Site 865 has excellent biostratigraphic age control over the interval ~38-55Ma. Preliminary data indicate an increase in the <span class="hlt">seawater</span> composition from 0.427 at 53.4 Ma to 0.499 by 43 Ma, consistent with the apparent trend in the few existing data points. We also analyzed the Os isotopic composition recorded by oxide minerals at Integrated Ocean Drilling Program (IODP) Site U1370</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22606412-sensing-response-copper-phthalocyanine-salt-dispersed-glass-organic-vapours','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22606412-sensing-response-copper-phthalocyanine-salt-dispersed-glass-organic-vapours"><span>Sensing response of copper phthalocyanine salt dispersed glass with organic <span class="hlt">vapours</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Ridhi, R.; Sachdeva, Sheenam; Saini, G. S. S.</p> <p>2016-05-06</p> <p>Copper Phthalocyanine and other Metal Phthalocyanines are very flexible and tuned easily to modify their structural, spectroscopic, optical and electrical properties by either functionalizing them with various substituent groups or by replacing or adding a ligand to the central metal atom in the phthalocyanine ring and accordingly can be made sensitive and selective to various organic species or gaseous <span class="hlt">vapours</span>. In the present work, we have dispersed Copper Phthalocyanine Salt (CuPcS) in sol-gel glass form using chemical route sol-gel method and studied its sensing mechanism with organic <span class="hlt">vapours</span> like methanol and benzene and found that current increases onto their exposuremore » with <span class="hlt">vapours</span>. A variation in the activation energies was also observed with exposure of <span class="hlt">vapours</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1983Cryo...23...15K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1983Cryo...23...15K"><span><span class="hlt">Vapour</span> phase motion in cryogenic systems containing superheated and subcooled liquids</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kirichenko, Yu. A.; Chernyakov, P. S.; Seregin, V. E.</p> <p></p> <p>The development of vent pipelines, and venting storage tanks for cryogenic liquids requires the knowledge of the law of motion as well as regularities of <span class="hlt">vapour</span> content variation in the liquid and heat dissipation by the <span class="hlt">vapour</span> phase. This is a theoretical study of the effect of superheating (subcooling) of the liquid, relative acceleration and reduced pressure upon the size and velocity of noninteracting <span class="hlt">vapour</span> bubbles, moving in the liquid, and upon their resistance and heat transfer coefficients.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012SPIE.8446E..3NK','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012SPIE.8446E..3NK"><span>A water <span class="hlt">vapour</span> monitor at Paranal Observatory</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kerber, Florian; Rose, Thomas; Chacón, Arlette; Cuevas, Omar; Czekala, Harald; Hanuschik, Reinhard; Momany, Yazan; Navarrete, Julio; Querel, Richard R.; Smette, Alain; van den Ancker, Mario E.; Cure, Michel; Naylor, David A.</p> <p>2012-09-01</p> <p>We present the performance characteristics of a water <span class="hlt">vapour</span> monitor that has been permanently deployed at ESO's Paranal observatory as a part of the VISIR upgrade project. After a careful analysis of the requirements and an open call for tender, the Low Humidity and Temperature Profiling microwave radiometer (LHATPRO), manufactured by Radiometer Physics GmbH (RPG), has been selected. The unit measures several channels across the strong water <span class="hlt">vapour</span> emission line at 183 GHz, necessary for resolving the low levels of precipitable water <span class="hlt">vapour</span> (PWV) that are prevalent on Paranal (median ~2.5 mm). The unit comprises the above humidity profiler (183-191 GHz), a temperature profiler (51-58 GHz), and an infrared radiometer (~10 μm) for cloud detection. The instrument has been commissioned during a 2.5 week period in Oct/Nov 2011, by comparing its measurements of PWV and atmospheric profiles with the ones obtained by 22 radiosonde balloons. In parallel an IR radiometer (Univ. Lethbridge) has been operated, and various observations with ESO facility spectrographs have been taken. The RPG radiometer has been validated across the range 0.5 - 9 mm demonstrating an accuracy of better than 0.1 mm. The saturation limit of the radiometer is about 20 mm. Currently, the radiometer is being integrated into the Paranal infrastructure to serve as a high time-resolution monitor in support of VLT science operations. The water <span class="hlt">vapour</span> radiometer's ability to provide high precision, high time resolution information on this important aspect of the atmosphere will be most useful for conducting IR observations with the VLT under optimal conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.H51C1271X','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.H51C1271X"><span>Numerical Study of Groundwater Flow and Salinity Distribution Cycling Controlled by <span class="hlt">Seawater</span>/Freshwater Interaction in Karst Aquifer Using <span class="hlt">SEAWAT</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Xu, Z.; Hu, B.</p> <p>2017-12-01</p> <p>The interest to predict <span class="hlt">seawater</span> intrusion and salinity distribution in Woodville Karst Plain (WKP) has increased due to the huge challenge on quality of drinkable water and serious environmental problems. <span class="hlt">Seawater</span> intrudes into the conduit system from submarine karst caves at Spring Creek Spring due to density difference and sea level rising, nowadays the low salinity has been detected at Wakulla Spring which is 18 km from coastal line. The groundwater discharge at two major springs and salinity distribution in this area is controlled by the <span class="hlt">seawater</span>/freshwater interaction under different rainfall conditions: during low rainfall periods, <span class="hlt">seawater</span> flow into the submarine spring through karst windows, then the salinity rising at the submarine spring leads to <span class="hlt">seawater</span> further intrudes into conduit system; during high rainfall periods, <span class="hlt">seawater</span> is pushed out by fresh water discharge at submarine spring. The previous numerical studies of WKP mainly focused on the density independent transport modeling and <span class="hlt">seawater</span>/freshwater discharge at major karst springs, in this study, a <span class="hlt">SEAWAT</span> model has been developed to fully investigate the salinity distribution in the WKP under repeating phases of low rainfall and high rainfall periods, the conduit system was simulated as porous media with high conductivity and porosity. The precipitation, salinity and discharge at springs were used to calibrate the model. The results showed that the salinity distribution in porous media and conduit system is controlled by the rainfall change, in general, the salinity distribution inland under low rainfall conditions is much higher and wider than the high rainfall conditions. The results propose a prediction on the environmental problem caused by <span class="hlt">seawater</span> intrusion in karst coastal aquifer, in addition, provide a visual and scientific basis for future groundwater remediation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2006AnGeo..24.1511M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2006AnGeo..24.1511M"><span>Stratospheric water <span class="hlt">vapour</span> in the vicinity of the Arctic polar vortex</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Maturilli, M.; Fierli, F.; Yushkov, V.; Lukyanov, A.; Khaykin, S.; Hauchecorne, A.</p> <p>2006-07-01</p> <p>The stratospheric water <span class="hlt">vapour</span> mixing ratio inside, outside, and at the edge of the polar vortex has been accurately measured by the FLASH-B Lyman-Alpha hygrometer during the LAUTLOS campaign in Sodankylä, Finland, in January and February 2004. The retrieved H2O profiles reveal a detailed view on the Arctic lower stratospheric water <span class="hlt">vapour</span> distribution, and provide a valuable dataset for the validation of model and satellite data. Analysing the measurements with the semi-lagrangian advection model MIMOSA, water <span class="hlt">vapour</span> profiles typical for the polar vortex' interior and exterior have been identified, and laminae in the observed profiles have been correlated to filamentary structures in the potential vorticity field. Applying the validated MIMOSA transport scheme to specific humidity fields from operational ECMWF analyses, large discrepancies from the observed profiles arise. Although MIMOSA is able to reproduce weak water <span class="hlt">vapour</span> filaments and improves the shape of the profiles compared to operational ECMWF analyses, both models reveal a dry bias of about 1 ppmv in the lower stratosphere above 400 K, accounting for a relative difference from the measurements in the order of 20%. The large dry bias in the analysis representation of stratospheric water <span class="hlt">vapour</span> in the Arctic implies the need for future regular measurements of water <span class="hlt">vapour</span> in the polar stratosphere to allow the validation and improvement of climate models.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003EAEJA.....8696L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003EAEJA.....8696L"><span>Preliminary data on formaldehyde content in <span class="hlt">seawater</span> samples from Terra Nova Bay (Ross Sea - Antarctica)</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Largiuni, O.; Becagli, S.; Traversi, R.; Udisti, R.</p> <p>2003-04-01</p> <p>Formaldehyde is a key reactive intermediate in the methane oxidation chain. To date, only a few measurements of HCHO in surface <span class="hlt">seawater</span> have been reported, suggesting a net flux of HCHO from the atmosphere to the ocean surface. Ocean is considered as a sink for atmospheric HCHO, but it cannot be excluded that marine areas characterized by high biogenic activity constitute a source of HCHO to atmosphere. Indeed, laboratory experiments carried out on <span class="hlt">seawater</span> microlayer show HCHO production by photo-oxidation of dissolved organic matter. To date no measurements on deep <span class="hlt">seawater</span> samples were performed. A sensitive method for the formaldehyde determination in aqueous sample by Flow Injection Analysis has been applied to <span class="hlt">seawater</span> samples analysis. The method has a detection limit of 55 ng/l and a reproducibility of 2.5% at 1 ug/l level (5 % in sea water samples). The detector response is linear in the range 0.1 - 3000 ug/l. In the framework of the Italian Research Programme in Antarctica (PNRA), 20 samples were collected in two stations in the Gerlache Inlet (Terra Nova Bay, Western Ross Sea) during the 2001/2002 field campaign (November 2001 to February 2002). The samples were collected through a hole in the sea-<span class="hlt">ice</span>, along the water column, using a Go-Flo type bottle. Usually, just sub-pack and 30 and 50 m depth fractions were collected. For each depth profile, temperature, salinity and chlorophyll fluorescence signal were measured. Formaldehyde concentrations range from 4.5 to 40 ppb. The relationship between HCHO content and other measured parameters is discussed. The sampling repetition in time at the same sites allowed evaluating the seasonal changes in the formaldehyde concentration/depth profiles.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_6");'>6</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li class="active"><span>8</span></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_8 --> <div id="page_9" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li class="active"><span>9</span></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="161"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018GeCoA.220...55P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018GeCoA.220...55P"><span>The stoichiometric dissociation constants of carbonic acid in <span class="hlt">seawater</span> brines from 298 to 267 K</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Papadimitriou, Stathys; Loucaides, Socratis; Rérolle, Victoire M. C.; Kennedy, Paul; Achterberg, Eric P.; Dickson, Andrew G.; Mowlem, Matthew; Kennedy, Hilary</p> <p>2018-01-01</p> <p>The stoichiometric dissociation constants of carbonic acid (K1C∗ and K2C∗) were determined by measurement of all four measurable parameters of the carbonate system (total alkalinity, total dissolved inorganic carbon, pH on the total proton scale, and CO2 fugacity) in natural <span class="hlt">seawater</span> and <span class="hlt">seawater</span>-derived brines, with a major ion composition equivalent to that of Reference <span class="hlt">Seawater</span>, to practical salinity (SP) 100 and from 25 °C to the freezing point of these solutions and -6 °C temperature minimum. These values, reported in the total proton scale, provide the first such determinations at below-zero temperatures and for SP > 50. The temperature (T, in Kelvin) and SP dependence of the current pK1C∗ and pK2C∗ (as negative common logarithms) within the salinity and temperature ranges of this study (33 ≤ SP ≤ 100, -6 °C ≤ t ≤ 25 °C) is described by the following best-fit equations: pK1C∗ = -176.48 + 6.14528 SP0.5 - 0.127714 SP + 7.396 × 10-5SP2 + (9914.37 - 622.886 SP0.5 + 29.714 SP) T-1 + (26.05129 - 0.666812 SP0.5) lnT (σ = 0.011, n = 62), and pK2C∗ = -323.52692 + 27.557655 SP0.5 + 0.154922 SP - 2.48396 × 10-4 SP2 + (14763.287 - 1014.819 SP0.5 - 14.35223 SP) T-1 + (50.385807 - 4.4630415 SP0.5) lnT (σ = 0.020, n = 62). These functions are suitable for application to investigations of the carbonate system of internal sea <span class="hlt">ice</span> brines with a conservative major ion composition relative to that of Reference <span class="hlt">Seawater</span> and within the temperature and salinity ranges of this study.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013INL.....3...99Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013INL.....3...99Z"><span>Physicochemical properties of protein-modified silver nanoparticles in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhong, Hangyue</p> <p>2013-10-01</p> <p>This study investigated the physicochemical properties of silver nanoparticles stabilized with casein protein in <span class="hlt">seawater</span>. UV?vis spectrometry, dynamic light scattering (DLS), and transmission electron microscopy (TEM) were applied to measure the stability of silver nanoparticles in <span class="hlt">seawater</span> samples. The obtained results show an increased aggregation tendency of silver nanoparticles in <span class="hlt">seawater</span>, which could be attributed its relatively high cation concentration that could neutralize the negatively charges adsorbed on the surface of silver nanoparticles and reduce the electrostatic repulsion forces between nanoparticles. Similarly, due to the surface charge screening process, the zeta potential of silver nanoparticles in <span class="hlt">seawater</span> decreased. This observation further supported the aggregation behavior of silver nanoparticles. This study also investigated the dissolution of silver nanoparticles in <span class="hlt">seawater</span>. Result shows that the silver nanoparticle dissolution in DI water is lower than in <span class="hlt">seawater</span>, which is attributed to the high Cl? concentration present in <span class="hlt">seawater</span>. As Cl? can react with silver and form soluble AgCl complex, dissolution of silver nanoparticles was enhanced. Finally, this study demonstrated that silver nanoparticles are destabilized in <span class="hlt">seawater</span> condition. These results may be helpful in understanding the environmental risk of discharged silver nanoparticles in <span class="hlt">seawater</span> conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMGC53H..04D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMGC53H..04D"><span>Arctic <span class="hlt">Ice</span> Management: an integrated approach to climate engineering</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Desch, S. J.; Hartnett, H. E.; Groppi, C. E.; Romaniello, S. J.</p> <p>2017-12-01</p> <p>The warming climate is having the most rapid and pronounced effects in the high Arctic. The loss of Arctic sea <span class="hlt">ice</span> is not only changing the physical oceanography of the Arctic Ocean and its coastlines; it is also promoting new conversations about the dangers and benefits for trade, transportation, and industry in the Arctic. The rate of decrease of summer sea <span class="hlt">ice</span> in the Arctic is currently -300 km3 yr-1, a rate that will lead to complete loss of end-summer sea <span class="hlt">ice</span> as soon as 2030. Preventing the strong positive feedbacks and increased warming due to sea <span class="hlt">ice</span> albedo loss must be an important component of climate mitigation strategies. Here, we explore a direct engineering approach we call Arctic <span class="hlt">Ice</span> Management (AIM) to reduce the loss of Arctic sea <span class="hlt">ice</span>. We predict that pumping <span class="hlt">seawater</span> onto the <span class="hlt">ice</span> surface during the Arctic winter using wind-powered pumps can thicken sea <span class="hlt">ice</span> by up to 1 m per year, reversing the current loss rates and prolonging the time until the Arctic Ocean is <span class="hlt">ice</span>-free. Thickening sea <span class="hlt">ice</span> would not change CO2 levels, which are the underlying cause of <span class="hlt">ice</span> loss, but it would prevent some of the strongest feedbacks and would buy time to develop the tools and governance systems necessary to achieve carbon-neutrality. We advocate exploration of AIM as a mitigation strategy employed in parallel with CO2 reduction efforts. The opportunity and risk profiles of AIM differ from other geoengineering proposals. While similar in principle to solar radiation management, AIM may present fewer large-scale environmental risks. AIM is separate from greenhouse gas emission reduction or sequestration, but might help prevent accelerated release of methane from thawing permafrost. Further, AIM might be usefully employed at regional and local scales to preserve Arctic ecosystems and possibly reduce the effects of <span class="hlt">ice</span>-loss induced coastal erosion. Through presentation of the AIM concept, we hope to spark new conversations between scientists, stakeholders, and decision</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5310029','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5310029"><span>Coral calcifying fluid pH is modulated by <span class="hlt">seawater</span> carbonate chemistry not solely <span class="hlt">seawater</span> pH</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Tambutté, E.; Carpenter, R. C.; Edmunds, P. J.; Evensen, N. R.; Allemand, D.; Ferrier-Pagès, C.; Tambutté, S.; Venn, A. A.</p> <p>2017-01-01</p> <p>Reef coral calcification depends on regulation of pH in the internal calcifying fluid (CF) in which the coral skeleton forms. However, little is known about calcifying fluid pH (pHCF) regulation, despite its importance in determining the response of corals to ocean acidification. Here, we investigate pHCF in the coral Stylophora pistillata in <span class="hlt">seawater</span> maintained at constant pH with manipulated carbonate chemistry to alter dissolved inorganic carbon (DIC) concentration, and therefore total alkalinity (AT). We also investigate the intracellular pH of calcifying cells, photosynthesis, respiration and calcification rates under the same conditions. Our results show that despite constant pH in the surrounding <span class="hlt">seawater</span>, pHCF is sensitive to shifts in carbonate chemistry associated with changes in [DIC] and [AT], revealing that <span class="hlt">seawater</span> pH is not the sole driver of pHCF. Notably, when we synthesize our results with published data, we identify linear relationships of pHCF with the <span class="hlt">seawater</span> [DIC]/[H+] ratio, [AT]/ [H+] ratio and []. Our findings contribute new insights into the mechanisms determining the sensitivity of coral calcification to changes in <span class="hlt">seawater</span> carbonate chemistry, which are needed for predicting effects of environmental change on coral reefs and for robust interpretations of isotopic palaeoenvironmental records in coral skeletons. PMID:28100813</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMPP41A2232K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMPP41A2232K"><span>A Continuous Flow Diffusion Chamber Study of Sea Salt Particles Acting as Cloud Seeds: Deliquescence, <span class="hlt">Ice</span> Nucleation and Sublimation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kong, X.; Wolf, M. J.; Garimella, S.; Roesch, M.; Cziczo, D. J.</p> <p>2016-12-01</p> <p>Sea Salt Aerosols (SSA) are abundant in the atmosphere, and important to the Earth's chemistry and energy budget. However, the roles of sea salts in the context of cloud formation are still poorly understood, which is partially due to the complexity of the water-salt phase diagram. At ambient temperatures, even well below 0°C, SSA deliquesces at sub-water saturated conditions. Since the ratio of the partial pressure over <span class="hlt">ice</span> versus super-cooled water continuously declines with decreasing temperatures, it is interesting to consider if SSA continues to deliquesce under a super-saturated condition of <span class="hlt">ice</span>, or if particles act as depositional <span class="hlt">ice</span> nuclei when a critical supersaturation is reached. Some recent studies suggest hydrated NaCl and simulated sea salt might deliquesce between -35°C to -44°C, and below that deposition freezing becomes possible. Deliquesced droplets can subsequently freeze via the immersion or homogenous freezing mode, depending on if the deliquescence processes is complete. After the droplets or <span class="hlt">ice</span> particles are formed, it is also interesting to consider how the different processes influence physical properties after evaporation or sublimation. This data is important for climate modeling that includes bromine burst observed in Antarctica, which is hypothesized to be relevant to the sublimation of blowing snow particles. In this study we use a SPectrometer for <span class="hlt">Ice</span> Nuclei (SPIN; DMT, Inc., Boulder, CO) to perform experiments over a wide range of temperature and RH conditions to quantify deliquescence, droplet formation and <span class="hlt">ice</span> nucleation. The formation of droplets and <span class="hlt">ice</span> particles is detected by an advanced Optical Particle Counter (OPC) and the liquid/solid phases are distinguished by a machine learning method based on laser scattering and polarization data. Using an atomizer, four different sea salt samples are generated: pure NaCl and MgCl2 solutions, synthetic <span class="hlt">seawater</span>, and natural <span class="hlt">seawater</span>. Downstream of the SPIN chamber, a Pumped</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.C43B0744A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.C43B0744A"><span>Spatial scales of light transmission through Antarctic pack <span class="hlt">ice</span>: Surface flooding vs. floe-size distribution</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Arndt, S.; Meiners, K.; Krumpen, T.; Ricker, R.; Nicolaus, M.</p> <p>2016-12-01</p> <p>Snow on sea <span class="hlt">ice</span> plays a crucial role for interactions between the ocean and atmosphere within the climate system of polar regions. Antarctic sea <span class="hlt">ice</span> is covered with snow during most of the year. The snow contributes substantially to the sea-<span class="hlt">ice</span> mass budget as the heavy snow loads can depress the <span class="hlt">ice</span> below water level causing flooding. Refreezing of the snow and <span class="hlt">seawater</span> mixture results in snow-<span class="hlt">ice</span> formation on the <span class="hlt">ice</span> surface. The snow cover determines also the amount of light being reflected, absorbed, and transmitted into the upper ocean, determining the surface energy budget of <span class="hlt">ice</span>-covered oceans. The amount of light penetrating through sea <span class="hlt">ice</span> into the upper ocean is of critical importance for the timing and amount of bottom sea-<span class="hlt">ice</span> melt, biogeochemical processes and under-<span class="hlt">ice</span> ecosystems. Here, we present results of several recent observations in the Weddell Sea measuring solar radiation under Antarctic sea <span class="hlt">ice</span> with instrumented Remotely Operated Vehicles (ROV). The combination of under-<span class="hlt">ice</span> optical measurements with simultaneous characterization of surface properties, such as sea-<span class="hlt">ice</span> thickness and snow depth, allows the identification of key processes controlling the spatial distribution of the under-<span class="hlt">ice</span> light. Thus, our results show how the distinction between flooded and non-flooded sea-<span class="hlt">ice</span> regimes dominates the spatial scales of under-<span class="hlt">ice</span> light variability for areas smaller than 100-by-100m. In contrast, the variability on larger scales seems to be controlled by the floe-size distribution and the associated lateral incidence of light. These results are related to recent studies on the spatial variability of Arctic under-<span class="hlt">ice</span> light fields focusing on the distinctly differing dominant surface properties between the northern (e.g. summer melt ponds) and southern (e.g. year-round snow cover, surface flooding) hemisphere sea-<span class="hlt">ice</span> cover.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21912788','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21912788"><span>Initiation of the <span class="hlt">ice</span> phase by marine biogenic surfaces in supersaturated gas and supercooled aqueous phases.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Alpert, Peter A; Aller, Josephine Y; Knopf, Daniel A</p> <p>2011-11-28</p> <p>Biogenic particles have the potential to affect the formation of <span class="hlt">ice</span> crystals in the atmosphere with subsequent consequences for the hydrological cycle and climate. We present laboratory observations of heterogeneous <span class="hlt">ice</span> nucleation in immersion and deposition modes under atmospherically relevant conditions initiated by Nannochloris atomus and Emiliania huxleyi, marine phytoplankton with structurally and chemically distinct cell walls. Temperatures at which freezing, melting, and water uptake occur are observed using optical microscopy. The intact and fragmented unarmoured cells of N. atomus in aqueous NaCl droplets enhance <span class="hlt">ice</span> nucleation by 10-20 K over the homogeneous freezing limit and can be described by a modified water activity based <span class="hlt">ice</span> nucleation approach. E. huxleyi cells covered by calcite plates do not enhance droplet freezing temperatures. Both species nucleate <span class="hlt">ice</span> in the deposition mode at an <span class="hlt">ice</span> saturation ratio, S(<span class="hlt">ice</span>), as low as ~1.2 and below 240 K, however, for each, different nucleation modes occur at warmer temperatures. These observations show that markedly different biogenic surfaces have both comparable and contrasting effects on <span class="hlt">ice</span> nucleation behaviour depending on the presence of the aqueous phase and the extent of supercooling and water <span class="hlt">vapour</span> supersaturation. We derive heterogeneous <span class="hlt">ice</span> nucleation rate coefficients, J(het), and cumulative <span class="hlt">ice</span> nuclei spectra, K, for quantification and analysis using time-dependent and time-independent approaches, respectively. Contact angles, α, derived from J(het)via immersion freezing depend on T, a(w), and S(<span class="hlt">ice</span>). For deposition freezing, α can be described as a function of S(<span class="hlt">ice</span>) only. The different approaches yield different predictions of atmospheric <span class="hlt">ice</span> crystal numbers primarily due to the time evolution allowed for the time-dependent approach with implications for the evolution of mixed-phase and <span class="hlt">ice</span> clouds.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2001AtmRe..58..295S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2001AtmRe..58..295S"><span>Impact of the Bergeron-Findeisen process on the release of aerosol particles during the evolution of cloud <span class="hlt">ice</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Schwarzenböck, A.; Mertes, S.; Heintzenberg, J.; Wobrock, W.; Laj, P.</p> <p></p> <p>The paper focuses on the redistribution of aerosol particles (APs) during the artificial nucleation and subsequent growth of <span class="hlt">ice</span> crystals in a supercooled cloud. A significant number of the supercooled cloud droplets during <span class="hlt">icing</span> periods (seeding agents: C 3H 8, CO 2) did not freeze as was presumed prior to the experiment but instead evaporated. The net mass flux of water <span class="hlt">vapour</span> from the evaporating droplets to the nucleating <span class="hlt">ice</span> crystals (Bergeron-Findeisen mechanism) led to the release of residual particles that simultaneously appeared in the interstitial phase. The strong decrease of the droplet residuals confirms the nucleation of <span class="hlt">ice</span> particles on seeding germs without natural aerosol particles serving as <span class="hlt">ice</span> nuclei. As the number of residual particles during the seedings did not drop to zero, other processes such as heterogeneous <span class="hlt">ice</span> nucleation, spontaneous freezing, entrainment of supercooled droplets and diffusion to the created particle-free <span class="hlt">ice</span> germs must have contributed to the experimental findings. During the <span class="hlt">icing</span> periods, residual mass concentrations in the condensed phase dropped by a factor of 1.1-6.7, as compared to the unperturbed supercooled cloud. As the Bergeron-Findeisen process also occurs without artificial seeding in the atmosphere, this study demonstrated that the hydrometeors in mixed-phase clouds might be much cleaner than anticipated for the simple freezing process of supercooled droplets in tropospheric mid latitude clouds.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AtmEn.141..255S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AtmEn.141..255S"><span>Technical note: Examining ozone deposition over <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sarwar, Golam; Kang, Daiwen; Foley, Kristen; Schwede, Donna; Gantt, Brett; Mathur, Rohit</p> <p>2016-09-01</p> <p>Surface layer resistance plays an important role in determining ozone deposition velocity over <span class="hlt">sea-water</span> and can be influenced by chemical interactions at the air-water interface. Here, we examine the effect of chemical interactions of iodide, dimethylsulfide, dissolved organic carbon, and bromide in <span class="hlt">seawater</span> on ozone deposition. We perform a series of simulations using the hemispheric Community Multiscale Air Quality model for summer months in the Northern Hemisphere. Our results suggest that each chemical interaction enhances the ozone deposition velocity and decreases the atmospheric ozone mixing ratio over <span class="hlt">seawater</span>. Iodide enhances the median deposition velocity over <span class="hlt">seawater</span> by 0.023 cm s-1, dissolved organic carbon by 0.021 cm s-1, dimethylsulfide by 0.002 cm s-1, and bromide by ∼0.0006 cm s-1. Consequently, iodide decreases the median atmospheric ozone mixing ratio over <span class="hlt">seawater</span> by 0.7 ppb, dissolved organic carbon by 0.8 ppb, dimethylsulfide by 0.1 ppb, and bromide by 0.02 ppb. In a separate model simulation, we account for the effect of dissolved salts in <span class="hlt">seawater</span> on the Henry's law constant for ozone and find that it reduces the median deposition velocity by 0.007 cm s-1 and increases surface ozone mixing ratio by 0.2 ppb. The combined effect of these processes increases the median ozone deposition velocity over <span class="hlt">seawater</span> by 0.040 cm s-1, lowers the atmospheric ozone mixing ratio by 5%, and slightly improves model performance relative to observations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010JPhD...43p5204H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010JPhD...43p5204H"><span>The dynamic effects of metal <span class="hlt">vapour</span> in gas metal arc welding</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Haidar, Jawad</p> <p>2010-04-01</p> <p>Numerical simulations for the dynamic effects of metal <span class="hlt">vapour</span> in gas metal arc welding (GMAW) suggest that <span class="hlt">vapour</span> from the welding droplet at the tip of the welding wire has a significant influence on the plasma properties. It is found that for the evaporation rates calculated for arcs in pure argon, the dynamic effects of metal <span class="hlt">vapour</span> markedly cool down the plasma in the central region of the arc, leading to the formation of a low temperature zone centred on the arc axis, in agreement with experimental measurements in the literature. Radiation effects, omitted in this paper, may produce further cooling of the plasma gas. The results highlight major deficiencies in the common approach to modelling the GMAW process and suggest that accurate description of GMAW must include the influence of metal <span class="hlt">vapour</span> on the plasma.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010NIMPB.268.1226A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010NIMPB.268.1226A"><span>Chlorine-36 in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Argento, David C.; Stone, John O.; Keith Fifield, L.; Tims, Stephen G.</p> <p>2010-04-01</p> <p>Natural cosmogenic 36Cl found in <span class="hlt">seawater</span> originates from spallation of atmospheric 40Ar, capture of secondary cosmic-ray neutrons by dissolved 35Cl, and river runoff which contains 36Cl produced in situ over the surface of the continents. The long residence time of chloride in the ocean and long half-life of 36Cl compared to the oceanic mixing time should result in a homogenous 36Cl/Cl ratio throughout the ocean. Production by neutron capture in the course of nuclear weapons testing should be insignificant averaged over the oceans as a whole, but may have led to regions of elevated 36Cl concentration. Previous attempts to measure the 36Cl/Cl ratio of <span class="hlt">seawater</span> have been hindered by interferences, contamination, or insufficient analytic sensitivity. Here we report preliminary measurements on <span class="hlt">seawater</span> samples, which demonstrate that the 36Cl/Cl ratio is 0.5 ± 0.3 × 10 -15, in reasonable agreement with calculated contributions from the sources listed above.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015EGUGA..1712862B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015EGUGA..1712862B"><span>GPS tomographic experiment on water <span class="hlt">vapour</span> dynamics in the troposphere over Lisbon</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Benevides, Pedro; Catalao, Joao; Miranda, Pedro</p> <p>2015-04-01</p> <p>Quantification of the water <span class="hlt">vapour</span> variability on the atmosphere remains a difficult task, affecting the weather prediction. Coarse water <span class="hlt">vapour</span> resolution measurements in space and time affect the numerical weather prediction solution models causing artifacts in the prediction of severe weather phenomena. The GNSS atmospheric processing has been developed in the past years providing integrated water <span class="hlt">vapour</span> estimates comparable with the meteorological sensor measurements, with studies registering 1 to 2 kg/m2 bias, but lack a vertical determination of the atmospheric processes. The GNSS tomography in the troposphere is one of the most promising techniques for sensing the three-dimensional water <span class="hlt">vapour</span> state of the atmosphere. The determination of the integrated water <span class="hlt">vapour</span> profile by means of the widely accepted GNSS meteorology techniques, allows the reconstruction of several slant path delay rays in the satellite line of view, providing an opportunity to sense the troposphere at tree-dimensions plus time. The tomographic system can estimate an image solution of the water <span class="hlt">vapour</span> but impositions have to be introduced to the system of equations inversion because of the non-optimal GNSS observation geometry. Application of this technique on atmospheric processes like large convective precipitation or mesoscale water <span class="hlt">vapour</span> circulation have been able to describe its local dynamic vertical variation. A 3D tomographic experiment was developed over an area of 60x60 km2 around Lisbon (Portugal). The GNSS network available composed by 9 receivers was used for an experiment of densification of the permanent network using 8 temporarily installed GPS receivers (totalling 17 stations). This study was performed during several weeks in July 2013, where a radiosonde campaign was also held in order to validate the tomographic inversion solution. 2D integrated water <span class="hlt">vapour</span> maps directly obtained from the GNSS processing were also evaluated and local coastal breeze circulation</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/916337','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/916337"><span>Measurements of the levels of organic solvent <span class="hlt">vapours</span> by personal air samplers and the levels of urinary metabolites of workers. Part 2. Toluene <span class="hlt">vapour</span> in a shipbuilding yard (author's transl).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kira, S</p> <p>1977-05-01</p> <p>Personal air samplers were applied to shipyard's painters putting on gas masks during the spraying work, and the levels of toluene <span class="hlt">vapour</span> surrounding the workers were measured. On the other hand, levels of urinary hippuric acid (metabolites of toluene) of the workers were measured, and the levels of toluene <span class="hlt">vapour</span> inhaled were calculated from the levels of urinary hippuric acid. Then the actual removing-efficiencies of toluene <span class="hlt">vapours</span> by the use of gas masks were estimated from these two levels (i.e., toluene <span class="hlt">vapours</span> exposed and inhaled). The values of removing-efficiencies were found to be 65.9-98.1%. The concentrations of hippuric and methylhippuric acids in the urine of workers exposed to toluene and xylene for 3 hours, collected just after the exposure, are valuable indices of these organic solvent <span class="hlt">vapours</span> inhaled. A minute amount of urinary methylhippuric acid can be determined by means of gas chromatography.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4209995','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4209995"><span>Antifreeze protein-induced superheating of <span class="hlt">ice</span> inside Antarctic notothenioid fishes inhibits melting during summer warming</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Cziko, Paul A.; DeVries, Arthur L.; Evans, Clive W.; Cheng, Chi-Hing Christina</p> <p>2014-01-01</p> <p>Antifreeze proteins (AFPs) of polar marine teleost fishes are widely recognized as an evolutionary innovation of vast adaptive value in that, by adsorbing to and inhibiting the growth of internalized environmental <span class="hlt">ice</span> crystals, they prevent death by inoculative freezing. Paradoxically, systemic accumulation of AFP-stabilized <span class="hlt">ice</span> could also be lethal. Whether or how fishes eliminate internal <span class="hlt">ice</span> is unknown. To investigate if <span class="hlt">ice</span> inside high-latitude Antarctic notothenioid fishes could melt seasonally, we measured its melting point and obtained a decadal temperature record from a shallow benthic fish habitat in McMurdo Sound, Antarctica. We found that AFP-stabilized <span class="hlt">ice</span> resists melting at temperatures above the expected equilibrium freezing/melting point (eqFMP), both in vitro and in vivo. Superheated <span class="hlt">ice</span> was directly observed in notothenioid serum samples and in solutions of purified AFPs, and <span class="hlt">ice</span> was found to persist inside live fishes at temperatures more than 1 °C above their eqFMP for at least 24 h, and at a lower temperature for at least several days. Field experiments confirmed that superheated <span class="hlt">ice</span> occurs naturally inside wild fishes. Over the long-term record (1999–2012), <span class="hlt">seawater</span> temperature surpassed the fish eqFMP in most summers, but never exceeded the highest temperature at which <span class="hlt">ice</span> persisted inside experimental fishes. Thus, because of the effects of AFP-induced melting inhibition, summer warming may not reliably eliminate internal <span class="hlt">ice</span>. Our results expose a potentially antagonistic pleiotropic effect of AFPs: beneficial freezing avoidance is accompanied by melting inhibition that may contribute to lifelong accumulation of detrimental internal <span class="hlt">ice</span> crystals. PMID:25246548</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25246548','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25246548"><span>Antifreeze protein-induced superheating of <span class="hlt">ice</span> inside Antarctic notothenioid fishes inhibits melting during summer warming.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cziko, Paul A; DeVries, Arthur L; Evans, Clive W; Cheng, Chi-Hing Christina</p> <p>2014-10-07</p> <p>Antifreeze proteins (AFPs) of polar marine teleost fishes are widely recognized as an evolutionary innovation of vast adaptive value in that, by adsorbing to and inhibiting the growth of internalized environmental <span class="hlt">ice</span> crystals, they prevent death by inoculative freezing. Paradoxically, systemic accumulation of AFP-stabilized <span class="hlt">ice</span> could also be lethal. Whether or how fishes eliminate internal <span class="hlt">ice</span> is unknown. To investigate if <span class="hlt">ice</span> inside high-latitude Antarctic notothenioid fishes could melt seasonally, we measured its melting point and obtained a decadal temperature record from a shallow benthic fish habitat in McMurdo Sound, Antarctica. We found that AFP-stabilized <span class="hlt">ice</span> resists melting at temperatures above the expected equilibrium freezing/melting point (eqFMP), both in vitro and in vivo. Superheated <span class="hlt">ice</span> was directly observed in notothenioid serum samples and in solutions of purified AFPs, and <span class="hlt">ice</span> was found to persist inside live fishes at temperatures more than 1 °C above their eqFMP for at least 24 h, and at a lower temperature for at least several days. Field experiments confirmed that superheated <span class="hlt">ice</span> occurs naturally inside wild fishes. Over the long-term record (1999-2012), <span class="hlt">seawater</span> temperature surpassed the fish eqFMP in most summers, but never exceeded the highest temperature at which <span class="hlt">ice</span> persisted inside experimental fishes. Thus, because of the effects of AFP-induced melting inhibition, summer warming may not reliably eliminate internal <span class="hlt">ice</span>. Our results expose a potentially antagonistic pleiotropic effect of AFPs: beneficial freezing avoidance is accompanied by melting inhibition that may contribute to lifelong accumulation of detrimental internal <span class="hlt">ice</span> crystals.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27159922','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27159922"><span><span class="hlt">Vapour</span> sensitivity of an ALD hierarchical photonic structure inspired by Morpho.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Poncelet, Olivier; Tallier, Guillaume; Mouchet, Sébastien R; Crahay, André; Rasson, Jonathan; Kotipalli, Ratan; Deparis, Olivier; Francis, Laurent A</p> <p>2016-05-09</p> <p>The unique architecture of iridescent Morpho butterfly scales is known to exhibit different optical responses to various <span class="hlt">vapours</span>. However, the mechanism behind this phenomenon is not fully quantitatively understood. This work reports on process developments in the micro-fabrication of a Morpho-inspired photonic structure in atomic layer deposited (ALD) materials in order to investigate the <span class="hlt">vapour</span> optical sensitivity of such artificial nanostructures. By developing recipes for dry and wet etching of ALD oxides, we micro-fabricated two structures: one combining Al2O3 and TiO2, and the other combining Al2O3 and HfO2. For the first time, we report the optical response of such ALD Morpho-like structures measured under a controlled flow of either ethanol or isopropyl alcohol (IPA) <span class="hlt">vapour</span>. In spite of the small magnitude of the effect, the results show a selective <span class="hlt">vapour</span> response (depending on the materials used).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2002AGUFMOS21B0194F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2002AGUFMOS21B0194F"><span>A Water Tank Study of the Effects of <span class="hlt">Seawater</span> Temperature on Coral Metabolism and Changes in Chemical Compositions in <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fujimura, H.; Arakaki, T.; Hamdun, A. M.; Oomori, T.</p> <p>2002-12-01</p> <p>For the past several years, large-scale coral bleaching has been observed in many coral reef areas around the world. Coral bleaching is considered to be caused mainly by high <span class="hlt">seawater</span> temperature together with other factors such as strong UV-light and changes in salinity. However, the mechanism of coral bleaching is not clearly understood. We have conducted experiments using water tanks under well-controlled light and temperature conditions to elucidate the effects of <span class="hlt">seawater</span> temperature on coral_fs metabolism and changes in chemical compositions in the <span class="hlt">seawater</span> around the coral. Metabolism of coral was studied by analyzing changes in <span class="hlt">seawater</span> chemical compositions. Coral specimen used in our experiment, Goniastrea aspera, was collected from northern shore of Okinawa island, Japan. pH, nitrate ion, dissolved organic carbon, and alkalinity were measured. Photochemically formed hydroxyl radical was also studied in those <span class="hlt">seawater</span> samples.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017GeCoA.213...17B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017GeCoA.213...17B"><span>Gypsum and hydrohalite dynamics in sea <span class="hlt">ice</span> brines</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Butler, Benjamin M.; Papadimitriou, Stathys; Day, Sarah J.; Kennedy, Hilary</p> <p>2017-09-01</p> <p>Mineral authigenesis from their dissolved sea salt matrix is an emergent feature of sea <span class="hlt">ice</span> brines, fuelled by dramatic equilibrium solubility changes in the large sub-zero temperature range of this cryospheric system on the surface of high latitude oceans. The multi-electrolyte composition of <span class="hlt">seawater</span> results in the potential for several minerals to precipitate in sea <span class="hlt">ice</span>, each affecting the in-situ geochemical properties of the sea <span class="hlt">ice</span> brine system, the habitat of sympagic biota. The solubility of two of these minerals, gypsum (CaSO4 ·2H2O) and hydrohalite (NaCl · 2H2O), was investigated in high ionic strength multi-electrolyte solutions at below-zero temperatures to examine their dissolution-precipitation dynamics in the sea <span class="hlt">ice</span> brine system. The gypsum dynamics in sea <span class="hlt">ice</span> were found to be highly dependent on the solubilities of mirabilite and hydrohalite between 0.2 and - 25.0 ° C. The hydrohalite solubility between - 14.3 and - 25.0 ° C exhibits a sharp change between undersaturated and supersaturated conditions, and, thus, distinct temperature fields of precipitation and dissolution in sea <span class="hlt">ice</span>, with saturation occurring at - 22.9 ° C. The sharp changes in hydrohalite solubility at temperatures ⩽-22.9 °C result from the formation of an <span class="hlt">ice</span>-hydrohalite aggregate, which alters the structural properties of brine inclusions in cold sea <span class="hlt">ice</span>. Favourable conditions for gypsum precipitation in sea <span class="hlt">ice</span> were determined to occur in the region of hydrohalite precipitation below - 22.9 ° C and in conditions of metastable mirabilite supersaturation above - 22.9 ° C (investigated at - 7.1 and - 8.2 ° C here) but gypsum is unlikely to persist once mirabilite forms at these warmer (>-22.9 °C) temperatures. The dynamics of hydrohalite in sea <span class="hlt">ice</span> brines based on its experimental solubility were consistent with that derived from thermodynamic modelling (FREZCHEM code) but the gypsum dynamics derived from the code were inconsistent with that indicated by its</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17375309','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17375309"><span><span class="hlt">Seawater</span> drinking restores water balance in dehydrated harp seals.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>How, Ole-Jakob; Nordøy, Erling S</p> <p>2007-07-01</p> <p>The purpose of this study was to answer the question of whether dehydrated harp seals (Phoca groenlandica) are able to obtain a net gain of water from the intake of <span class="hlt">seawater</span>. Following 24 h of fasting, three subadult female harp seals were dehydrated by intravenous administration of the osmotic diuretic, mannitol. After another 24 h of fasting, the seals were given 1,000 ml <span class="hlt">seawater</span> via a stomach tube. Urine and blood were collected for measurement of osmolality and osmolytes, while total body water (TBW) was determined by injections of tritiated water. In all seals, the maximum urinary concentrations of Na(+) and Cl(-) were higher than in <span class="hlt">seawater</span>, reaching 540 and 620 mM, respectively, compared to 444 and 535 mM in <span class="hlt">seawater</span>. In another experiment, the seals were given ad lib access to <span class="hlt">seawater</span> for 48 h after mannitol-induced hyper-osmotic dehydration. In animals without access to <span class="hlt">seawater</span>, the mean blood osmolality increased from 331 to 363 mOsm kg(-1) during dehydration. In contrast, the blood osmolality, hematocrit and TBW returned to normal when the seals were permitted ad lib access to <span class="hlt">seawater</span> after dehydration. In conclusion, this study shows that harp seals have the capacity to gain net water from mariposa (voluntarily drinking <span class="hlt">seawater</span>) and are able to restore water balance after profound dehydration by drinking <span class="hlt">seawater</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5734650','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5734650"><span>Vertical structure of stratospheric water <span class="hlt">vapour</span> trends derived from merged satellite data</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Hegglin, M. I.; Plummer, D. A.; Shepherd, T. G.; Scinocca, J. F.; Anderson, J.; Froidevaux, L.; Funke, B.; Hurst, D.; Rozanov, A.; Urban, J.; von Clarmann, T.; Walker, K. A.; Wang, H. J.; Tegtmeier, S.; Weigel, K.</p> <p>2017-01-01</p> <p>Stratospheric water <span class="hlt">vapour</span> is a powerful greenhouse gas. The longest available record from balloon observations over Boulder, Colorado, USA shows increases in stratospheric water <span class="hlt">vapour</span> concentrations that cannot be fully explained by observed changes in the main drivers, tropical tropopause temperatures and methane. Satellite observations could help resolve the issue, but constructing a reliable long-term data record from individual short satellite records is challenging. Here we present an approach to merge satellite data sets with the help of a chemistry-climate model nudged to observed meteorology. We use the models' water <span class="hlt">vapour</span> as a transfer function between data sets that overcomes issues arising from instrument drift and short overlap periods. In the lower stratosphere, our water <span class="hlt">vapour</span> record extends back to 1988 and water <span class="hlt">vapour</span> concentrations largely follow tropical tropopause temperatures. Lower and mid-stratospheric long-term trends are negative, and the trends from Boulder are shown not to be globally representative. In the upper stratosphere, our record extends back to 1986 and shows positive long-term trends. The altitudinal differences in the trends are explained by methane oxidation together with a strengthened lower-stratospheric and a weakened upper-stratospheric circulation inferred by this analysis. Our results call into question previous estimates of surface radiative forcing based on presumed global long-term increases in water <span class="hlt">vapour</span> concentrations in the lower stratosphere. PMID:29263751</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_7");'>7</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li class="active"><span>9</span></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_9 --> <div id="page_10" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="181"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29263751','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29263751"><span>Vertical structure of stratospheric water <span class="hlt">vapour</span> trends derived from merged satellite data.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hegglin, M I; Plummer, D A; Shepherd, T G; Scinocca, J F; Anderson, J; Froidevaux, L; Funke, B; Hurst, D; Rozanov, A; Urban, J; von Clarmann, T; Walker, K A; Wang, H J; Tegtmeier, S; Weigel, K</p> <p>2014-01-01</p> <p>Stratospheric water <span class="hlt">vapour</span> is a powerful greenhouse gas. The longest available record from balloon observations over Boulder, Colorado, USA shows increases in stratospheric water <span class="hlt">vapour</span> concentrations that cannot be fully explained by observed changes in the main drivers, tropical tropopause temperatures and methane. Satellite observations could help resolve the issue, but constructing a reliable long-term data record from individual short satellite records is challenging. Here we present an approach to merge satellite data sets with the help of a chemistry-climate model nudged to observed meteorology. We use the models' water <span class="hlt">vapour</span> as a transfer function between data sets that overcomes issues arising from instrument drift and short overlap periods. In the lower stratosphere, our water <span class="hlt">vapour</span> record extends back to 1988 and water <span class="hlt">vapour</span> concentrations largely follow tropical tropopause temperatures. Lower and mid-stratospheric long-term trends are negative, and the trends from Boulder are shown not to be globally representative. In the upper stratosphere, our record extends back to 1986 and shows positive long-term trends. The altitudinal differences in the trends are explained by methane oxidation together with a strengthened lower-stratospheric and a weakened upper-stratospheric circulation inferred by this analysis. Our results call into question previous estimates of surface radiative forcing based on presumed global long-term increases in water <span class="hlt">vapour</span> concentrations in the lower stratosphere.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70155975','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70155975"><span>Water <span class="hlt">vapour</span> correction of the daily 1 km AVHRR global land dataset: Part I validation and use of the Water <span class="hlt">Vapour</span> input field</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>DeFelice, Thomas P.; Lloyd, D.; Meyer, D.J.; Baltzer, T. T.; Piraina, P.</p> <p>2003-01-01</p> <p>An atmospheric correction algorithm developed for the 1 km Advanced Very High Resolution Radiometer (AVHRR) global land dataset was modified to include a near real-time total column water <span class="hlt">vapour</span> data input field to account for the natural variability of atmospheric water <span class="hlt">vapour</span>. The real-time data input field used for this study is the Television and Infrared Observational Satellite (TIROS) Operational Vertical Sounder (TOVS) Pathfinder A global total column water <span class="hlt">vapour</span> dataset. It was validated prior to its use in the AVHRR atmospheric correction process using two North American AVHRR scenes, namely 13 June and 28 November 1996. The validation results are consistent with those reported by others and entail a comparison between TOVS, radiosonde, experimental sounding, microwave radiometer, and data from a hand-held sunphotometer. The use of this data layer as input to the AVHRR atmospheric correction process is discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20010022375','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20010022375"><span>EOS Aqua AMSR-E Sea <span class="hlt">Ice</span> Validation Program: Meltpond2000 Flight Report</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Cavalieri, Donald J.</p> <p>2000-01-01</p> <p>This flight report describes the field component of Meltpond2000, the first in a series of Arctic and Antarctic aircraft campaigns planned as part of NASA's Earth Observing System Aqua sea <span class="hlt">ice</span> validation program for the Advanced Microwave Scanning Radiometer (AMSR-E). This prelaunch Arctic field campaign was carried out between June 25 and July 6, 2000 from Thule, Greenland, with the objective of quantifying the errors incurred by the AMSR-E sea <span class="hlt">ice</span> algorithms resulting from the presence of melt ponds. A secondary objective of the mission was to develop a microwave capability to discriminate between melt ponds and <span class="hlt">seawater</span> using low-frequency microwave radiometers. Meltpond2000 was a multiagency effort involving personnel from the Navy, NOAA, and NASA. The field component of the mission consisted of making five 8-hour flights from Thule Air Base with a Naval Air Warfare Center P-3 aircraft over portions of Baffin Bay and the Canadian Arctic. The aircraft sensors were provided and operated by the Microwave Radiometry Group of NOAA's Environmental TechnologyLaboratory. A Navy <span class="hlt">ice</span> observer from the National <span class="hlt">Ice</span> Center provided visual documentation of surface <span class="hlt">ice</span> conditions during each of the flights. Two of the five flights were coordinated with Canadian scientists making surface measurements of melt ponds at an <span class="hlt">ice</span> camp located near Resolute Bay, Canada. Coordination with the Canadians will provide additional information on surface characteristics and will be of great value in the interpretation of the aircraft and high-resolution satellite data sets.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018AIPC.1953c0172R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018AIPC.1953c0172R"><span>Spectroscopic interaction studies of substituted and unsubstituted copper phthalocyanine with adsorbed organic <span class="hlt">vapours</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ridhi, R.; Kang, Jasmeen; Saini, G. S. S.; Tripathi, S. K.</p> <p>2018-05-01</p> <p>The present study deals with comparing the interaction mechanism of adsorbed organic <span class="hlt">vapours</span> with Copper Phthalocyanine thin films in its substituted and unsubstituted forms. For this purpose, the variations in vibrational levels of substituted CuPc (CuPcS) functionalized with tetrasulfonic acid tetrasodium salt and unsubstituted CuPc after exposure with methanol and benzene <span class="hlt">vapours</span> is analyzed. Fourier transform infrared (FTIR) is used to study the interaction behaviour. The bulkier group tetrasulfonic acid tetrasodium salt added to CuPc leads to occupation of more space in the molecular arrangement as compared to unsubstituted CuPc and hence alteration of its properties. FTIR spectra of CuPc and CuPcS before and after <span class="hlt">vapours</span> exposures highlighted the effect of these <span class="hlt">vapours</span> on the various bonds and the role of functional group in altering the molecular structure of CuPcS during interaction with adsorbed <span class="hlt">vapours</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2002AGUFMOS12B0282B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2002AGUFMOS12B0282B"><span>Field Results for an Arctic AUV Designed for Characterizing Circulation and <span class="hlt">Ice</span> Thickness</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bellingham, J. G.; Kirkwood, W. J.; Tervalon, N.; Cokelet, E.; Thomas, H.; Sibenac, M.; Gashler, D.; McEwen, R.; Henthorn, R.; Shane, F.; Osborn, D. J.; Johnson, K.; Overland, J.; Stein, P.; Bahlavouni, A.; Anderson, D.</p> <p>2002-12-01</p> <p>An Autonomous Underwater Vehicle designed for operation at high latitudes and under <span class="hlt">ice</span> completed its first Arctic field tests from the USCGC Healy in fall of 2001. The ALTEX AUV has been under development since 1998, and is being created to provide: unprecedented endurance, ability to navigate at high latitudes, a depth rating of 1500 to 4500 meters depending on payload, and the capability to relay data through the <span class="hlt">ice</span> to satellites via data buoys. The AUV's initial applications are focused on tracking the warm Atlantic Layer inflow - the primary source of <span class="hlt">seawater</span> to the Arctic Ocean. Consequently the primary payloads are twin pumped CTD systems. Oxygen and nitrate sensors provide the ability to use NO as a tracer. An <span class="hlt">ice</span> profiling sonar allows the AUV to estimate the <span class="hlt">ice</span> thickness in real-time and is designed to generate high quality post-processed <span class="hlt">ice</span> draft data comparable to that collected through the SCICEX program. The experiments in October aboard the USCGC Healy generated numerous water column and under-<span class="hlt">ice</span> data sets. Traditional ship-based CTD operations were used to provide a comparison data set for AUV water column measurements. The post-processed <span class="hlt">ice</span> draft results show reasonable <span class="hlt">ice</span> profiles and have the potential, when combined with other science data collected, to shed some additional light on upper water column processes in <span class="hlt">ice</span>-covered regions. Cruise results include: operating the AUV from the USCGC Healy in the <span class="hlt">ice</span> pack, demonstrating inertial navigation system performance, obtaining oceanographic sections with the AUV, obtaining <span class="hlt">ice</span> draft measurements with an AUV born sonar, and testing the data-buoy system. This work is supported by the National Science Foundation under grant NSF-OPP 9910290. The Packard Foundation and the Office of Naval Research have also provided support. The project was initiated under the National Ocean Partnership Program under contract N00014-98-1-0814.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28100813','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28100813"><span>Coral calcifying fluid pH is modulated by <span class="hlt">seawater</span> carbonate chemistry not solely <span class="hlt">seawater</span> pH.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Comeau, S; Tambutté, E; Carpenter, R C; Edmunds, P J; Evensen, N R; Allemand, D; Ferrier-Pagès, C; Tambutté, S; Venn, A A</p> <p>2017-01-25</p> <p>Reef coral calcification depends on regulation of pH in the internal calcifying fluid (CF) in which the coral skeleton forms. However, little is known about calcifying fluid pH (pH CF ) regulation, despite its importance in determining the response of corals to ocean acidification. Here, we investigate pH CF in the coral Stylophora pistillata in <span class="hlt">seawater</span> maintained at constant pH with manipulated carbonate chemistry to alter dissolved inorganic carbon (DIC) concentration, and therefore total alkalinity (A T ). We also investigate the intracellular pH of calcifying cells, photosynthesis, respiration and calcification rates under the same conditions. Our results show that despite constant pH in the surrounding <span class="hlt">seawater</span>, pH CF is sensitive to shifts in carbonate chemistry associated with changes in [DIC] and [A T ], revealing that <span class="hlt">seawater</span> pH is not the sole driver of pH CF Notably, when we synthesize our results with published data, we identify linear relationships of pH CF with the <span class="hlt">seawater</span> [DIC]/[H + ] ratio, [A T ]/ [H + ] ratio and [[Formula: see text</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013TCry....7..707R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013TCry....7..707R"><span>Ikaite crystal distribution in winter sea <span class="hlt">ice</span> and implications for CO2 system dynamics</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rysgaard, S.; Søgaard, D. H.; Cooper, M.; Pućko, M.; Lennert, K.; Papakyriakou, T. N.; Wang, F.; Geilfus, N. X.; Glud, R. N.; Ehn, J.; McGinnis, D. F.; Attard, K.; Sievers, J.; Deming, J. W.; Barber, D.</p> <p>2013-04-01</p> <p>The precipitation of ikaite (CaCO3 ⋅ 6H2O) in polar sea <span class="hlt">ice</span> is critical to the efficiency of the sea <span class="hlt">ice</span>-driven carbon pump and potentially important to the global carbon cycle, yet the spatial and temporal occurrence of ikaite within the <span class="hlt">ice</span> is poorly known. We report unique observations of ikaite in unmelted <span class="hlt">ice</span> and vertical profiles of ikaite abundance and concentration in sea <span class="hlt">ice</span> for the crucial season of winter. <span class="hlt">Ice</span> was examined from two locations: a 1 m thick land-fast <span class="hlt">ice</span> site and a 0.3 m thick polynya site, both in the Young Sound area (74° N, 20° W) of NE Greenland. Ikaite crystals, ranging in size from a few μm to 700 μm, were observed to concentrate in the interstices between the <span class="hlt">ice</span> platelets in both granular and columnar sea <span class="hlt">ice</span>. In vertical sea <span class="hlt">ice</span> profiles from both locations, ikaite concentration determined from image analysis, decreased with depth from surface-<span class="hlt">ice</span> values of 700-900 μmol kg-1 <span class="hlt">ice</span> (~25 × 106 crystals kg-1) to values of 100-200 μmol kg-1 <span class="hlt">ice</span> (1-7 × 106 crystals kg-1) near the sea <span class="hlt">ice</span>-water interface, all of which are much higher (4-10 times) than those reported in the few previous studies. Direct measurements of total alkalinity (TA) in surface layers fell within the same range as ikaite concentration, whereas TA concentrations in the lower half of the sea <span class="hlt">ice</span> were twice as high. This depth-related discrepancy suggests interior <span class="hlt">ice</span> processes where ikaite crystals form in surface sea <span class="hlt">ice</span> layers and partly dissolve in layers below. Melting of sea <span class="hlt">ice</span> and dissolution of observed concentrations of ikaite would result in meltwater with a pCO2 of <15 μatm. This value is far below atmospheric values of 390 μatm and surface water concentrations of 315 μatm. Hence, the meltwater increases the potential for <span class="hlt">seawater</span> uptake of CO2.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24015106','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24015106"><span>Antifungal activity of clove essential oil and its volatile <span class="hlt">vapour</span> against dermatophytic fungi.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Chee, Hee Youn; Lee, Min Hee</p> <p>2007-12-01</p> <p>Antifungal activities of clove essential oil and its volatile <span class="hlt">vapour</span> against dermatophytic fungi including Candida albicans, Epidermophyton floccosum. Microsporum audouinii, Trichophyton mentagrophytes, and Trichophyton rubrum were investigated. Both clove essential oil and its volatile <span class="hlt">vapour</span> strongly inhibit spore germination and mycelial growth of the dermatophytic fungi tested. The volatile <span class="hlt">vapour</span> of clove essential oil showed fungistatic activity whereas direct application of clove essential oil showed fungicidal activity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADC951313','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADC951313"><span>Post-Contamination <span class="hlt">Vapour</span> Hazards from Military Vehicles Contaminated with Thickened and Unthickened GD</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>1979-02-01</p> <p>The residual <span class="hlt">vapour</span> hazards from four types of military vehicles previously contaminated with either thickened or unthickened GD have been measured...magnitude of these hazards have been investigated and an assessment made of their relevance to contamination control. It was found that on permeable... contamination had been applied were ineffective in reducing the subsequent <span class="hlt">vapour</span> hazard; the <span class="hlt">vapour</span> hazard arising from thickened GD contamination was less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFMOS54A..02J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFMOS54A..02J"><span>Buffer capacity, ecosystem feedbacks, and <span class="hlt">seawater</span> chemistry under global change</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Jury, C. P.; Thomas, F. I.; Atkinson, M. J.; Jokiel, P. L.; Onuma, M. A.; Kaku, N.; Toonen, R. J.</p> <p>2013-12-01</p> <p>Ocean acidification (OA) results in reduced <span class="hlt">seawater</span> pH and aragonite saturation state (Ωarag), but also reduced <span class="hlt">seawater</span> buffer capacity. As buffer capacity decreases, diel variation in <span class="hlt">seawater</span> chemistry increases. However, a variety of ecosystem feedbacks can modulate changes in both average <span class="hlt">seawater</span> chemistry and diel <span class="hlt">seawater</span> chemistry variation. Here we model these effects for a coastal, reef flat ecosystem. We show that an increase in offshore pCO2 and temperature (to 900 μatm and +3°C) can increase diel pH variation by as much as a factor of 2.5 and can increase diel pCO2 variation by a factor of 4.6, depending on ecosystem feedbacks and <span class="hlt">seawater</span> residence time. Importantly, these effects are different between day and night. With increasing <span class="hlt">seawater</span> residence time and increasing feedback intensity, daytime <span class="hlt">seawater</span> chemistry becomes more similar to present-day conditions while nighttime <span class="hlt">seawater</span> chemistry becomes less similar to present-day conditions. Better constraining ecosystem feedbacks under global change will improve projections of coastal water chemistry, but this study shows the importance of considering changes in both average carbonate chemistry and diel chemistry variation for organisms and ecosystems. Further, we will discuss our recent work examining the effects of diel <span class="hlt">seawater</span> chemistry variation on coral calcification rates.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSHE34A1464B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSHE34A1464B"><span>An Investigation of Mineral Dynamics in Sea <span class="hlt">Ice</span> by Solubility Measurements</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Butler, B.; Kennedy, H.; Papadimitriou, S.</p> <p>2016-02-01</p> <p>Sea <span class="hlt">ice</span> is a composite material with a sponge-like structure. The framework of the structure is composed of pure <span class="hlt">ice</span>, and within the pores exists a concentrated <span class="hlt">seawater</span> brine. When the temperature is reduced, the volume of this residual brine decreases, while its salinity increases. As a result of the paired changes to temperature and salinity, the brine becomes supersaturated with respect to a mineral at several points when cooling sea <span class="hlt">ice</span> towards -30°C, creating a sequence of minerals that precipitate. The presence of countless microscopic salt crystals encapsulated within the <span class="hlt">ice</span>, coupled with changes in brine volume associated with their precipitation/dissolution, results in changes to the optical and structural properties of the medium that contribute to the surface energy balance in sea <span class="hlt">ice</span> environments. Furthermore, attainment of mineral equilibrium can result in abrupt changes in brine composition and osmotic conditions in the isolated brine pockets, imposing challenging conditions upon the biota that habitat the sea <span class="hlt">ice</span> environment. Mirabilite (Na2SO4.10H2O), gypsum (CaSO4.2H2O) and hydrohalite (NaCl.2H2O) each represent minerals that are understood to exist within sea <span class="hlt">ice</span>. Previous research has focused upon mineral extraction/detection, and the specific temperature for the onset of each minerals precipitation in sea <span class="hlt">ice</span>; rather than the overarching dynamics. For this reason, solubility measurements of mirabilite, gypsum and hydrohalite in conditions representative of equilibrium sea <span class="hlt">ice</span> brines were carried between 0 and -28°C, covering a range of undersaturated and supersaturated conditions for each mineral. Results provide accurate data for the onset of each minerals formation in sea <span class="hlt">ice</span>, as well as important information on the way in which precipitation and dissolution reactions are affected when sea <span class="hlt">ice</span> warms or cools. By incorporating the solubility data into a model that simluates the temperature-salinity profiles of first-year sea <span class="hlt">ice</span>, the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20150008266','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20150008266"><span>The Seasonal Cycle of Water <span class="hlt">Vapour</span> on Mars from Assimilation of Thermal Emission Spectrometer Data</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Steele, Liam J.; Lewis, Stephen R.; Patel, Manish R.; Montmessin, Franck; Forget, Francois; Smith, Michael D.</p> <p>2014-01-01</p> <p>We present for the first time an assimilation of Thermal Emission Spectrometer (TES) water <span class="hlt">vapour</span> column data into a Mars global climate model (MGCM). We discuss the seasonal cycle of water <span class="hlt">vapour</span>, the processes responsible for the observed water <span class="hlt">vapour</span> distribution, and the cross-hemispheric water transport. The assimilation scheme is shown to be robust in producing consistent reanalyses, and the global water <span class="hlt">vapour</span> column error is reduced to around 2-4 pr micron depending on season. Wave activity is shown to play an important role in the water <span class="hlt">vapour</span> distribution, with topographically steered flows around the Hellas and Argyre basins acting to increase transport in these regions in all seasons. At high northern latitudes, zonal wavenumber 1 and 2 stationary waves during northern summer are responsible for spreading the sublimed water <span class="hlt">vapour</span> away from the pole. Transport by the zonal wavenumber 2 waves occurs primarily to the west of Tharsis and Arabia Terra and, combined with the effects of western boundary currents, this leads to peak water <span class="hlt">vapour</span> column abundances here as observed by numerous spacecraft. A net transport of water to the northern hemisphere over the course of one Mars year is calculated, primarily because of the large northwards flux of water <span class="hlt">vapour</span> which occurs during the local dust storm around L(sub S) = 240-260deg. Finally, outlying frost deposits that surround the north polar cap are shown to be important in creating the peak water <span class="hlt">vapour</span> column abundances observed during northern summer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSMM44B0489O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSMM44B0489O"><span>Proteolytic enzymes in <span class="hlt">seawater</span>: contribution of prokaryotes and protists</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Obayashi, Y.; Suzuki, S.</p> <p>2016-02-01</p> <p>Proteolytic enzyme is one of the major catalysts of microbial processing of organic matter in biogeochemical cycle. Here we summarize some of our studies about proteases in <span class="hlt">seawater</span>, including 1) distribution of protease activities in coastal and oceanic <span class="hlt">seawater</span>, 2) responses of microbial community and protease activities in <span class="hlt">seawater</span> to organic matter amending, and 3) possible contribution of heterotrophic protists besides prokaryotes to proteases in <span class="hlt">seawater</span>, to clarify cleared facts and remaining questions. Activities of aminopeptidases, trypsin-type and chymotrypsin-type proteases were detected from both coastal and oceanic <span class="hlt">seawater</span> by using MCA-substrate assay. Significant activities were detected from not only particulate (cell-associated) fraction but also dissolved fraction of <span class="hlt">seawater</span>, especially for trypsin-type and chymotrypsin-type proteases. Hydrolytic enzymes in <span class="hlt">seawater</span> have been commonly thought to be mainly derived from heterotrophic prokaryotes; however, it was difficult to determine actual source organisms of dissolved enzymes in natural <span class="hlt">seawater</span>. Our experiment with addition of dissolved protein to subtropical oligotrophic Pacific water showed drastically enhancement of the protease activities especially aminopeptidases in <span class="hlt">seawater</span>, and the prokaryotic community structure simultaneously changed to be dominant of Bacteroidetes, indicating that heterotrophic bacteria were actually one of the sources of proteases in <span class="hlt">seawater</span>. Another microcosm experiment with free-living marine heterotrophic ciliate Paranophrys marina together with an associated bacterium showed that extracellular trypsin-type activity was mainly attributed to the ciliate. The protist seemed to work in organic matter digestion in addition to be a grazer. From the results, we propose a system of organic matter digestion by prokaryotes and protists in aquatic environments, although their actual contribution in natural environments should be estimated in future studies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JPCS..115..119R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JPCS..115..119R"><span>Comparison of interaction mechanisms of copper phthalocyanine and nickel phthalocyanine thin films with chemical <span class="hlt">vapours</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ridhi, R.; Singh, Sukhdeep; Saini, G. S. S.; Tripathi, S. K.</p> <p>2018-04-01</p> <p>The present study deals with comparing interaction mechanisms of copper phthalocyanine and nickel phthalocyanine with versatile chemical <span class="hlt">vapours</span>: reducing, stable aromatic and oxidizing <span class="hlt">vapours</span> namely; diethylamine, benzene and bromine. The variation in electrical current of phthalocyanines with exposure of chemical <span class="hlt">vapours</span> is used as the detection parameter for studying interaction behaviour. Nickel phthalocyanine is found to exhibit anomalous behaviour after exposure of reducing <span class="hlt">vapour</span> diethylamine due to alteration in its spectroscopic transitions and magnetic states. The observed sensitivities of copper phthalocyanine and nickel phthalcyanine films are different in spite of their similar bond numbers, indicating significant role of central metal atom in interaction mechanism. The variations in electronic transition levels after <span class="hlt">vapours</span> exposure, studied using UV-Visible spectroscopy confirmed our electrical sensing results. Bromine exposure leads to significant changes in vibrational bands of metal phthalocyanines as compared to other <span class="hlt">vapours</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JGRE..123..180V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JGRE..123..180V"><span>Geophysical Investigations of Habitability in <span class="hlt">Ice</span>-Covered Ocean Worlds</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Vance, Steven D.; Panning, Mark P.; Stähler, Simon; Cammarano, Fabio; Bills, Bruce G.; Tobie, Gabriel; Kamata, Shunichi; Kedar, Sharon; Sotin, Christophe; Pike, William T.; Lorenz, Ralph; Huang, Hsin-Hua; Jackson, Jennifer M.; Banerdt, Bruce</p> <p>2018-01-01</p> <p>Geophysical measurements can reveal the structures and thermal states of icy ocean worlds. The interior density, temperature, sound speed, and electrical conductivity thus characterize their habitability. We explore the variability and correlation of these parameters using 1-D internal structure models. We invoke thermodynamic consistency using available thermodynamics of aqueous MgSO4, NaCl (as <span class="hlt">seawater</span>), and NH3; pure water <span class="hlt">ice</span> phases I, II, III, V, and VI; silicates; and any metallic core that may be present. Model results suggest, for Europa, that combinations of geophysical parameters might be used to distinguish an oxidized ocean dominated by MgSO4 from a more reduced ocean dominated by NaCl. In contrast with Jupiter's icy ocean moons, Titan and Enceladus have low-density rocky interiors, with minimal or no metallic core. The low-density rocky core of Enceladus may comprise hydrated minerals or anhydrous minerals with high porosity. <fi>Cassini</fi> gravity data for Titan indicate a high tidal potential Love number (k2>0.6), which requires a dense internal ocean (ρocean>1,200 kg m-3) and icy lithosphere thinner than 100 km. In that case, Titan may have little or no high-pressure <span class="hlt">ice</span>, or a surprisingly deep water-rock interface more than 500 km below the surface, covered only by <span class="hlt">ice</span> VI. Ganymede's water-rock interface is the deepest among known ocean worlds, at around 800 km. Its ocean may contain multiple phases of high-pressure <span class="hlt">ice</span>, which will become buoyant if the ocean is sufficiently salty. Callisto's interior structure may be intermediate to those of Titan and Europa, with a water-rock interface 250 km below the surface covered by <span class="hlt">ice</span> V but not <span class="hlt">ice</span> VI.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016ACP....16.6547L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016ACP....16.6547L"><span>Impact of major volcanic eruptions on stratospheric water <span class="hlt">vapour</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Löffler, Michael; Brinkop, Sabine; Jöckel, Patrick</p> <p>2016-05-01</p> <p>Volcanic eruptions can have a significant impact on the Earth's weather and climate system. Besides the subsequent tropospheric changes, the stratosphere is also influenced by large eruptions. Here changes in stratospheric water <span class="hlt">vapour</span> after the two major volcanic eruptions of El Chichón in Mexico in 1982 and Mount Pinatubo on the Philippines in 1991 are investigated with chemistry-climate model simulations. This study is based on two simulations with specified dynamics of the European Centre for Medium-Range Weather Forecasts Hamburg - Modular Earth Submodel System (ECHAM/MESSy) Atmospheric Chemistry (EMAC) model, performed within the Earth System Chemistry integrated Modelling (ESCiMo) project, of which only one includes the long-wave volcanic forcing through prescribed aerosol optical properties. The results show a significant increase in stratospheric water <span class="hlt">vapour</span> induced by the eruptions, resulting from increased heating rates and the subsequent changes in stratospheric and tropopause temperatures in the tropics. The tropical vertical advection and the South Asian summer monsoon are identified as sources for the additional water <span class="hlt">vapour</span> in the stratosphere. Additionally, volcanic influences on tropospheric water <span class="hlt">vapour</span> and El Niño-Southern Oscillation (ENSO) are evident, if the long-wave forcing is strong enough. Our results are corroborated by additional sensitivity simulations of the Mount Pinatubo period with reduced nudging and reduced volcanic aerosol extinction.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25930052','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25930052"><span>Effects of NaCl and <span class="hlt">seawater</span> induced salinity on survival and reproduction of three soil invertebrate species.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Pereira, C S; Lopes, I; Sousa, J P; Chelinho, S</p> <p>2015-09-01</p> <p>The increase of global mean temperature is raising serious concerns worldwide due to its potential negative effects such as droughts and melting of glaciers and <span class="hlt">ice</span> caps leading to sea level rise. Expected impacts on soil compartment include floodings, <span class="hlt">seawater</span> intrusions and use of saltwater for irrigation, with unknown effects on soil ecosystems and their inhabitants. The present study aimed at evaluating the effects of salinisation on soil ecosystems due to sea level rise. The reproduction and mortality of three standard soil invertebrate species (Folsomia candida, Enchytraeus crypticus, Hypoaspis aculeifer) in standard artificial OECD soil spiked with serial dilutions of <span class="hlt">seawater</span>/gradient of NaCl were evaluated according to standard guidelines. An increased sensitivity was observed in the following order: H. aculeifer≪E. crypticus≈F. candida consistent with the different exposure pathways: springtails and enchytraeids are exposed by ingestion and contact while mites are mainly exposed by ingestion due to a continuous and thick exoskeleton. Although small differences were observed in the calculated effect electrical conductivity values, <span class="hlt">seawater</span> and NaCl induced the same overall effects (with a difference in the enchytraeid tests where a higher sensitivity was found in relation to NaCl). The adverse effects described in the present study are observed on soils not considered saline. Therefore, the actual limit to define saline soils (4000 μS cm(-1)) does not reflect the existing knowledge when considering soil fauna. Copyright © 2015 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23467656','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23467656"><span>Levels of selected carcinogens and toxicants in <span class="hlt">vapour</span> from electronic cigarettes.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Goniewicz, Maciej Lukasz; Knysak, Jakub; Gawron, Michal; Kosmider, Leon; Sobczak, Andrzej; Kurek, Jolanta; Prokopowicz, Adam; Jablonska-Czapla, Magdalena; Rosik-Dulewska, Czeslawa; Havel, Christopher; Jacob, Peyton; Benowitz, Neal</p> <p>2014-03-01</p> <p>Electronic cigarettes, also known as e-cigarettes, are devices designed to imitate regular cigarettes and deliver nicotine via inhalation without combusting tobacco. They are purported to deliver nicotine without other toxicants and to be a safer alternative to regular cigarettes. However, little toxicity testing has been performed to evaluate the chemical nature of <span class="hlt">vapour</span> generated from e-cigarettes. The aim of this study was to screen e-cigarette <span class="hlt">vapours</span> for content of four groups of potentially toxic and carcinogenic compounds: carbonyls, volatile organic compounds, nitrosamines and heavy metals. <span class="hlt">Vapours</span> were generated from 12 brands of e-cigarettes and the reference product, the medicinal nicotine inhaler, in controlled conditions using a modified smoking machine. The selected toxic compounds were extracted from <span class="hlt">vapours</span> into a solid or liquid phase and analysed with chromatographic and spectroscopy methods. We found that the e-cigarette <span class="hlt">vapours</span> contained some toxic substances. The levels of the toxicants were 9-450 times lower than in cigarette smoke and were, in many cases, comparable with trace amounts found in the reference product. Our findings are consistent with the idea that substituting tobacco cigarettes with e-cigarettes may substantially reduce exposure to selected tobacco-specific toxicants. E-cigarettes as a harm reduction strategy among smokers unwilling to quit, warrants further study. (To view this abstract in Polish and German, please see the supplementary files online.).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014GeCoA.134..317H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014GeCoA.134..317H"><span>The major-ion composition of Carboniferous <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Holt, Nora M.; García-Veigas, Javier; Lowenstein, Tim K.; Giles, Peter S.; Williams-Stroud, Sherilyn</p> <p>2014-06-01</p> <p>The major-ion chemistry (Na+, Mg2+, Ca2+, K+, SO42-, and Cl-) of Carboniferous <span class="hlt">seawater</span> was determined from chemical analyses of fluid inclusions in marine halites, using the cryo scanning electron microscopy (Cryo-SEM) X-ray energy-dispersive spectrometry (EDS) technique. Fluid inclusions in halite from the Mississippian Windsor and Mabou Groups, Shubenacadie Basin, Nova Scotia, Canada (Asbian and Pendleian Substages, 335.5-330 Ma), and from the Pennsylvanian Paradox Formation, Utah, USA, (Desmoinesian Stage 309-305 Ma) contain Na+-Mg2+-K+-Ca2+-Cl- brines, with no measurable SO42-, which shows that the Carboniferous ocean was a “CaCl2 sea”, relatively enriched in Ca2+ and low in SO42- with equivalents Ca2+ > SO42- + HCO3-. δ34S values from anhydrite in the Mississippian Shubenacadie Basin (13.2-14.0 ‰) and the Pennsylvanian Paradox Formation (11.2-12.6 ‰) support <span class="hlt">seawater</span> sources. Br in halite from the Shubenacadie Basin (53-111 ppm) and the Paradox Basin (68-147 ppm) also indicate <span class="hlt">seawater</span> parentages. Carboniferous <span class="hlt">seawater</span>, modeled from fluid inclusions, contained ∼22 mmol Ca2+/kg H2O (Mississippian) and ∼24 mmol Ca2+/kg H2O (Pennsylvanian). Estimated sulfate concentrations are ∼14 mmol SO42-/kg H2O (Mississippian), and ∼12 mmol SO42-/kg H2O (Pennsylvanian). Calculated Mg2+/Ca2+ ratios are 2.5 (Mississippian) and 2.3 (Pennsylvanian), with an estimated range of 2.0-3.2. The fluid inclusion record of <span class="hlt">seawater</span> chemistry shows a long period of CaCl2 seas in the Paleozoic, from the Early Cambrian through the Carboniferous, when <span class="hlt">seawater</span> was enriched in Ca2+ and relatively depleted in SO42-. During this ∼200 Myr interval, Ca2+ decreased and SO42- increased, but did not cross the Ca2+-SO42- chemical divide to become a MgSO4 sea (when SO42- in <span class="hlt">seawater</span> became greater than Ca2+) until the latest Pennsylvanian or earliest Permian (∼309-295 Ma). <span class="hlt">Seawater</span> remained a MgSO4 sea during the Permian and Triassic, for ∼100 Myr. Fluid inclusions also record</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPhD...50QLT03P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPhD...50QLT03P"><span>Mixing of multiple metal <span class="hlt">vapours</span> into an arc plasma in gas tungsten arc welding of stainless steel</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Park, Hunkwan; Trautmann, Marcus; Tanaka, Keigo; Tanaka, Manabu; Murphy, Anthony B.</p> <p>2017-11-01</p> <p>A computational model of the mixing of multiple metal <span class="hlt">vapours</span>, formed by vaporization of the surface of an alloy workpiece, into the thermal arc plasma in gas tungsten arc welding (GTAW) is presented. The model incorporates the combined diffusion coefficient method extended to allow treatment of three gases, and is applied to treat the transport of both chromium and iron <span class="hlt">vapour</span> in the helium arc plasma. In contrast to previous models of GTAW, which predict that metal <span class="hlt">vapours</span> are swept away to the edge of the arc by the plasma flow, it is found that the metal <span class="hlt">vapours</span> penetrate strongly into the arc plasma, reaching the cathode region. The predicted results are consistent with published measurements of the intensity of atomic line radiation from the metal <span class="hlt">vapours</span>. The concentration of chromium <span class="hlt">vapour</span> is predicted to be higher than that of iron <span class="hlt">vapour</span> due to its larger vaporization rate. An accumulation of chromium <span class="hlt">vapour</span> is predicted to occur on the cathode at about 1.5 mm from the cathode tip, in agreement with published measurements. The arc temperature is predicted to be strongly reduced due to the strong radiative emission from the metal <span class="hlt">vapours</span>. The driving forces causing the diffusion of metal <span class="hlt">vapours</span> into the helium arc are examined, and it is found that diffusion due to the applied electric field (cataphoresis) is dominant. This is explained in terms of large ionization energies and the small mass of helium compared to those of the metal <span class="hlt">vapours</span>.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_8");'>8</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li class="active"><span>10</span></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_10 --> <div id="page_11" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="201"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015InAgr..29..115O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015InAgr..29..115O"><span>Kinetic model of water <span class="hlt">vapour</span> adsorption by gluten-free starch</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ocieczek, Aneta; Kostek, Robert; Ruszkowska, Millena</p> <p>2015-01-01</p> <p>This study evaluated the kinetics of water <span class="hlt">vapour</span> adsorption on the surface of starch molecules derived from wheat. The aim of the study was to determine an equation that would allow estimation of water content in tested material in any timepoint of the adsorption process aimed at settling a balance with the environment. An adsorption isotherm of water <span class="hlt">vapour</span> on starch granules was drawn. The parameters of the Guggenheim, Anderson, and De Boer equation were determined by characterizing the tested product and adsorption process. The equation of kinetics of water <span class="hlt">vapour</span> adsorption on the surface of starch was determined based on the Guggenheim, Anderson, and De Boer model describing the state of equilibrium and on the model of a first-order linear inert element describing the changes in water content over time.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015MolPh.113.2742V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015MolPh.113.2742V"><span>Mechanism of two-step <span class="hlt">vapour</span>-crystal nucleation in a pore</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>van Meel, J. A.; Liu, Y.; Frenkel, D.</p> <p>2015-09-01</p> <p>We present a numerical study of the effect of hemispherical pores on the nucleation of Lennard-Jones crystals from the <span class="hlt">vapour</span> phase. As predicted by Page and Sear, there is a narrow range of pore radii, where <span class="hlt">vapour</span>-liquid nucleation can become a two-step process. A similar observation was made for different pore geometries by Giacomello et al. We find that the maximum nucleation rate depends on both the size and the adsorption strength of the pore. Moreover, a poe can be more effective than a planar wall with the same strength of attraction. Pore-induced <span class="hlt">vapour</span>-liquid nucleation turns out to be the rate-limiting step for crystal nucleation. This implies that crystal nucleation can be enhanced by a judicious choice of the wetting properties of a microporous nucleating agent.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017Sci...355.1069H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017Sci...355.1069H"><span>The geologic history of <span class="hlt">seawater</span> pH</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Halevy, I.; Bachan, A.</p> <p>2017-03-01</p> <p>Although pH is a fundamental property of Earth’s oceans, critical to our understanding of <span class="hlt">seawater</span> biogeochemistry, its long-timescale geologic history is poorly constrained. We constrain <span class="hlt">seawater</span> pH through time by accounting for the cycles of the major components of <span class="hlt">seawater</span>. We infer an increase from early Archean pH values between ~6.5 and 7.0 and Phanerozoic values between ~7.5 and 9.0, which was caused by a gradual decrease in atmospheric pCO2 in response to solar brightening, alongside a decrease in hydrothermal exchange between <span class="hlt">seawater</span> and the ocean crust. A lower pH in Earth’s early oceans likely affected the kinetics of chemical reactions associated with the origin of life, the energetics of early metabolisms, and climate through the partitioning of CO2 between the oceans and atmosphere.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3682974','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3682974"><span><span class="hlt">Seawater</span>-Cultured Botryococcus braunii for Efficient Hydrocarbon Extraction</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Furuhashi, Kenichi; Saga, Kiyotaka; Okada, Shigeru; Imou, Kenji</p> <p>2013-01-01</p> <p>As a potential source of biofuel, the green colonial microalga Botryococcus braunii produces large amounts of hydrocarbons that are accumulated in the extracellular matrix. Generally, pretreatment such as drying or heating of wet algae is needed for sufficient recoveries of hydrocarbons from B. braunii using organic solvents. In this study, the Showa strain of B. braunii was cultured in media derived from the modified Chu13 medium by supplying artificial <span class="hlt">seawater</span>, natural <span class="hlt">seawater</span>, or NaCl. After a certain period of culture in the media with an osmotic pressure corresponding to 1/4-<span class="hlt">seawater</span>, hydrocarbon recovery rates exceeding 90% were obtained by simply mixing intact wet algae with n-hexane without any pretreatments and the results using the present culture conditions indicate the potential for hydrocarbon milking. Highlights <span class="hlt">Seawater</span> was used for efficient hydrocarbon extraction from Botryococcus braunii. The alga was cultured in media prepared with <span class="hlt">seawater</span> or NaCl. Hydrocarbon recovery rate exceeding 90% was obtained without any pretreatment. PMID:23799107</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23799107','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23799107"><span><span class="hlt">Seawater</span>-cultured Botryococcus braunii for efficient hydrocarbon extraction.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Furuhashi, Kenichi; Saga, Kiyotaka; Okada, Shigeru; Imou, Kenji</p> <p>2013-01-01</p> <p>As a potential source of biofuel, the green colonial microalga Botryococcus braunii produces large amounts of hydrocarbons that are accumulated in the extracellular matrix. Generally, pretreatment such as drying or heating of wet algae is needed for sufficient recoveries of hydrocarbons from B. braunii using organic solvents. In this study, the Showa strain of B. braunii was cultured in media derived from the modified Chu13 medium by supplying artificial <span class="hlt">seawater</span>, natural <span class="hlt">seawater</span>, or NaCl. After a certain period of culture in the media with an osmotic pressure corresponding to 1/4-<span class="hlt">seawater</span>, hydrocarbon recovery rates exceeding 90% were obtained by simply mixing intact wet algae with n-hexane without any pretreatments and the results using the present culture conditions indicate the potential for hydrocarbon milking. <span class="hlt">Seawater</span> was used for efficient hydrocarbon extraction from Botryococcus braunii. The alga was cultured in media prepared with <span class="hlt">seawater</span> or NaCl. Hydrocarbon recovery rate exceeding 90% was obtained without any pretreatment.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017SPIE10568E..04G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017SPIE10568E..04G"><span>WALES: water <span class="hlt">vapour</span> lidar experiment in space</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Guerin, F.; Pain, Th.; Palmade, J.-L.; Pailharey, E.; Giraud, D.; Jubineau, F.</p> <p>2017-11-01</p> <p>The WAter <span class="hlt">vapour</span> Lidar Experiment in Space (WALES) mission aims at providing water <span class="hlt">vapour</span> profiles with high accuracy and vertical resolution through the troposphere and the lower stratosphere on a global scale using an instrument based on Differential Absorption Lidar (DIAL) observation technique, and mounted on an Earth orbiting satellite. This active DIAL technique will also provide data on the cloud coverage by means of the signal reflection on the cloud layers. In DIAL operation, backscatter lidar signals at two wavelengths - at least - are detected. One wavelength (λ ON) is highly absorbed by the species of interest, while the other (λ OFF) is backscattered with minimal absorption. This difference in absorption at the two transmitted wavelengths leads to the determination of the concentration of the species of interest. The DIAL is therefore a dual-wavelength lidar in which the signals detected at the two wavelengths are processed to extract the absolute density of water <span class="hlt">vapour</span>. The Phase A study performed by ALCATEL Space and their partners under contract of the European Space Agency has led to a credible and innovative concept of instrument, based on a mission performance modelling. The challenge is to foster the scientific return while minimising the development risks and costs of instrument development, in particular the laser transmitter. The paper describes the payload design and the implementation on a low Earth orbiting (LEO) satellite.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004ESASP.554...25G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004ESASP.554...25G"><span>WALES: WAter <span class="hlt">vapour</span> Lidar Experiment in Space</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Guerin, F.; Pain, Th.; Palmade, J. L.; Pailharey, E.; Giraud, D.; Jubineau, F.</p> <p>2004-06-01</p> <p>The WAter <span class="hlt">vapour</span> Lidar Experiment in Space (WALES) mission aims at providing water <span class="hlt">vapour</span> profiles with high accuracy and vertical resolution through the troposphere and the lower stratosphere on a global scale using an instrument based on Differential Absorption Lidar (DIAL) observation technique, and mounted on an Earth orbiting satellite. This active DIAL technique will also provide data on the cloud coverage by means of the signal reflection on the cloud layers. In DIAL operation, backscatter lidar signals at two wavelengths - at least - are detected. One wavelength (λ ON) is highly absorbed by the species of interest, while the other (λ OFF) is backscattered with minimal absorption. This difference in absorption at the two transmitted wavelengths leads to the determination of the concentration of the species of interest. The DIAL is therefore a dual-wavelength lidar in which the signals detected at the two wavelengths are processed to extract the absolute density of water <span class="hlt">vapour</span>. The Phase A study performed by ALCATEL Space and their partners under contract of the European Space Agency has led to a credible and innovative concept of instrument, based on a mission performance modelling. The challenge is to foster the scientific return while minimising the development risks and costs of instrument development, in particular the laser transmitter. The paper describes the payload design and the implementation on a low Earth orbiting (LEO) satellite.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=312039&Lab=NERL&keyword=simulation+AND+processes&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=312039&Lab=NERL&keyword=simulation+AND+processes&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>Chemical effect on ozone deposition over <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Surface layer resistance plays an important role in determining ozone deposition velocity over <span class="hlt">seawater</span>. Recent studies suggest that surface layer resistance over <span class="hlt">sea-water</span> is influenced by wind-speed and chemical interaction at the air-water interface. Here, we investigate the e...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29041667','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29041667"><span>Towards quantum communications in free-space <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ji, Ling; Gao, Jun; Yang, Ai-Lin; Feng, Zhen; Lin, Xiao-Feng; Li, Zhong-Gen; Jin, Xian-Min</p> <p>2017-08-21</p> <p>Long-distance quantum channels capable of transferring quantum states faithfully for unconditionally secure quantum communication have been so far confirmed to be feasible in both fiber and free-space air. However, it remains unclear whether <span class="hlt">seawater</span>, which covers more than 70% of the earth, can also be utilized, leaving global quantum communication incomplete. Here we experimentally demonstrate that polarization quantum states including general qubits of single photon and entangled states can survive well after travelling through <span class="hlt">seawater</span>. We perform experiments with <span class="hlt">seawater</span> collected over a range of 36 kilometers in the Yellow Sea. For single photons at 405 nm in a blue-green window, we obtain an average process fidelity above 98%. For entangled photons at 810nm, albeit very high loss, we observe the violation of Bell inequality with 33 standard deviations. Our results confirm the feasibility of a <span class="hlt">seawater</span> quantum channel, representing the first step towards underwater quantum communication.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1440441-unsaturation-vapour-pressure-inside-leaves-two-conifer-species','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1440441-unsaturation-vapour-pressure-inside-leaves-two-conifer-species"><span>Unsaturation of <span class="hlt">vapour</span> pressure inside leaves of two conifer species</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Cernusak, Lucas A.; Ubierna, Nerea; Jenkins, Michael W.; ...</p> <p>2018-05-16</p> <p>Stomatal conductance (g s) impacts both photosynthesis and transpiration, and is therefore fundamental to the global carbon and water cycles, food production, and ecosystem services. Mathematical models provide the primary means of analysing this important leaf gas exchange parameter. A nearly universal assumption in such models is that the <span class="hlt">vapour</span> pressure inside leaves (e i) remains saturated under all conditions. The validity of this assumption has not been well tested, because so far e i cannot be measured directly. Here, we test this assumption using a novel technique, based on coupled measurements of leaf gas exchange and the stable isotopemore » compositions of CO 2 and water <span class="hlt">vapour</span> passing over the leaf. We applied this technique to mature individuals of two semiarid conifer species. In both species, e i routinely dropped below saturation when leaves were exposed to moderate to high air <span class="hlt">vapour</span> pressure deficits. Typical values of relative humidity in the intercellular air spaces were as low 0.9 in Juniperus monosperma and 0.8 in Pinus edulis. These departures of e i from saturation caused significant biases in calculations of g s and the intercellular CO 2 concentration. Thus, our results refute the longstanding assumption of saturated <span class="hlt">vapour</span> pressure in plant leaves under all conditions.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1440441','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1440441"><span>Unsaturation of <span class="hlt">vapour</span> pressure inside leaves of two conifer species</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Cernusak, Lucas A.; Ubierna, Nerea; Jenkins, Michael W.</p> <p></p> <p>Stomatal conductance (g s) impacts both photosynthesis and transpiration, and is therefore fundamental to the global carbon and water cycles, food production, and ecosystem services. Mathematical models provide the primary means of analysing this important leaf gas exchange parameter. A nearly universal assumption in such models is that the <span class="hlt">vapour</span> pressure inside leaves (e i) remains saturated under all conditions. The validity of this assumption has not been well tested, because so far e i cannot be measured directly. Here, we test this assumption using a novel technique, based on coupled measurements of leaf gas exchange and the stable isotopemore » compositions of CO 2 and water <span class="hlt">vapour</span> passing over the leaf. We applied this technique to mature individuals of two semiarid conifer species. In both species, e i routinely dropped below saturation when leaves were exposed to moderate to high air <span class="hlt">vapour</span> pressure deficits. Typical values of relative humidity in the intercellular air spaces were as low 0.9 in Juniperus monosperma and 0.8 in Pinus edulis. These departures of e i from saturation caused significant biases in calculations of g s and the intercellular CO 2 concentration. Thus, our results refute the longstanding assumption of saturated <span class="hlt">vapour</span> pressure in plant leaves under all conditions.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20020013322','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20020013322"><span>EOS Aqua AMSR-E Sea <span class="hlt">Ice</span> Validation Program: Meltpond 2000 Flight Report</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Cavalieri, Donald J.</p> <p>2000-01-01</p> <p>This flight report describes the field component of Meltpond2000, the first in a series of Arctic and Antarctic aircraft campaigns planned as part of NASA's Earth Observing System Aqua sea <span class="hlt">ice</span> validation program for the Advanced Microwave Scanning Radiometer (AMSR-E). This prelaunch Arctic field campaign was carried out between June 25 and July 6, 2000 from Thule, Greenland, with the objective of quantifying the errors incurred by the AMSR-E sea <span class="hlt">ice</span> algorithms resulting from the presence of melt ponds. A secondary objective of the mission was to develop a microwave capability to discriminate between melt ponds and <span class="hlt">seawater</span> using low-frequency microwave radiometers. Meltpond2000 was a multiagency effort involving personnel from the Navy, National Oceanic and Atmospheric Administration (NOAA), and NASA. The field component of the mission consisted of making five eight-hour flights from Thule Air Base with a Naval Air Warfare Center P-3 aircraft over portions of Baffin Bay and the Canadian Arctic. The aircraft sensors were provided and operated by the Microwave Radiometry Group of NOAA's Environmental Technology Laboratory. A Navy <span class="hlt">ice</span> observer from the National <span class="hlt">Ice</span> Center provided visual documentation of surface <span class="hlt">ice</span> conditions during each of the flights. Two of the five flights were coordinated with Canadian scientists making surface measurements of melt ponds at an <span class="hlt">ice</span> camp located near Resolute Bay, Canada. Coordination with the Canadians will provide additional information on surface characteristics and will be of great value in the interpretation of the aircraft and high-resolution satellite data sets.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26ES..108b2037H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26ES..108b2037H"><span>Corrosion and Protection of Metal in the <span class="hlt">Seawater</span> Desalination</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hou, Xiangyu; Gao, Lili; Cui, Zhendong; Yin, Jianhua</p> <p>2018-01-01</p> <p><span class="hlt">Seawater</span> desalination develops rapid for it can solve water scarcity efficiently. However, corrosion problem in the <span class="hlt">seawater</span> desalination system is more serious than that in normal water. So, it is important to pay attention to the corrosion and protection of metal in <span class="hlt">seawater</span> desalination. The corrosion characteristics and corrosion types of metal in the <span class="hlt">seawater</span> desalination system are introduced in this paper; In addition, corrosion protect methods and main influencing factors are stated, the latest new technologies about anti-corrosion with quantum energy assisted and magnetic inhibitor are presented.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1999GeoRL..26..871K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1999GeoRL..26..871K"><span>Implication of azelaic acid in a Greenland <span class="hlt">Ice</span> Core for oceanic and atmospheric changes in high latitudes</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kawamura, K.; Yokoyama, K.; Fujii, Y.; Watanabe, O.</p> <p></p> <p>A Greenland <span class="hlt">ice</span> core (450 years) has been studied for low molecular weight dicarboxylic acids (C2-C10) using a capillary gas chromatography and mass spectrometer. Their molecular distribution generally showed a predominance of succinic acid (C4) followed by oxalic (C2), malonic (C3), glutaric (C5), adipic (C6), and azelaic (C9) acids. Azelaic acid, that is a specific photochemical reaction product of biogenic unsaturated fatty acids, gave a characteristic historical trend in the <span class="hlt">ice</span> core; i.e., the concentrations are relatively low during late 16th to 19th century (Little <span class="hlt">Ice</span> Age) but become very high in late 19th to 20th century (warmer periods) with a large peak in 1940s AD. Lower concentrations of azelaic acid may have been caused by a depressed emission of unsaturated fatty acids from <span class="hlt">seawater</span> microlayers due to enhanced sea <span class="hlt">ice</span> coverage during Little <span class="hlt">Ice</span> Age. Inversely, increased concentrations of azelaic acid in late 19th to 20th century are likely interpreted by an enhanced sea-to-air emission of the precursor unsaturated fatty acids due to a retreat of sea <span class="hlt">ice</span> and/or by the enhanced production due to a potentially increased oxidizing capability of the atmosphere.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018ACP....18.4463N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018ACP....18.4463N"><span>Water <span class="hlt">vapour</span> and methane coupling in the stratosphere observed using SCIAMACHY solar occultation measurements</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Noël, Stefan; Weigel, Katja; Bramstedt, Klaus; Rozanov, Alexei; Weber, Mark; Bovensmann, Heinrich; Burrows, John P.</p> <p>2018-04-01</p> <p>An improved stratospheric water <span class="hlt">vapour</span> data set has been retrieved from SCIAMACHY/ENVISAT solar occultation measurements. It is similar to that successfully applied to methane and carbon dioxide. There is now a consistent set of data products for the three constituents covering the altitudes 17-45 km, the latitude range between about 50 and 70° N, and the period August 2002 to April 2012. The new water <span class="hlt">vapour</span> concentration profiles agree with collocated results from ACE-FTS and MLS/Aura to within ˜ 5 %. A significant positive linear change in water <span class="hlt">vapour</span> for the time 2003-2011 is observed at lower stratospheric altitudes with a value of about 0.015 ± 0.008 ppmv year-1 around 17 km. Between 30 and 37 km the changes become significantly negative (about -0.01 ± 0.008 ppmv year-1); all errors are 2σ values. The combined analysis of the SCIAMACHY methane and water <span class="hlt">vapour</span> time series shows the expected anti-correlation between stratospheric methane and water <span class="hlt">vapour</span> and a clear temporal variation related to the Quasi-Biennial Oscillation (QBO). Above about 20 km most of the additional water <span class="hlt">vapour</span> is attributed to the oxidation of methane. In addition short-term fluctuations and longer-term variations on a timescale of 5-6 years are observed. The SCIAMACHY data confirm that at lower altitudes the amount of water <span class="hlt">vapour</span> and methane are transported from the tropics to higher latitudes via the shallow branch of the Brewer-Dobson circulation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18620916','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18620916"><span>High-accuracy determination of iron in <span class="hlt">seawater</span> by isotope dilution multiple collector inductively coupled plasma mass spectrometry (ID-MC-ICP-MS) using nitrilotriacetic acid chelating resin for pre-concentration and matrix separation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>de Jong, Jeroen; Schoemann, Véronique; Lannuzel, Delphine; Tison, Jean-Louis; Mattielli, Nadine</p> <p>2008-08-15</p> <p>In the present paper we describe a robust and simple method to measure dissolved iron (DFe) concentrations in <span class="hlt">seawater</span> down to <0.1 nmol L(-1) level, by isotope dilution multiple collector inductively coupled plasma mass spectrometry (ID-MC-ICP-MS) using a (54)Fe spike and measuring the (57)Fe/(54)Fe ratio. The method provides for a pre-concentration step (100:1) by micro-columns filled with the resin NTA Superflow of 50 mL <span class="hlt">seawater</span> samples acidified to pH 1.9. NTA Superflow is demonstrated to quantitatively extract Fe from acidified <span class="hlt">seawater</span> samples at this pH. Blanks are kept low (grand mean 0.045+/-0.020 nmol L(-1), n=21, 3 x S.D. limit of detection per session 0.020-0.069 nmol L(-1) range), as no buffer is required to adjust the sample pH for optimal extraction, and no other reagents are needed than ultrapure nitric acid, 12 mM H(2)O(2), and acidified (pH 1.9) ultra-high purity (UHP) water. We measured SAFe (sampling and analysis of Fe) reference <span class="hlt">seawater</span> samples Surface-1 (0.097+/-0.043 nmol L(-1)) and Deep-2 (0.91+/-0.17 nmol L(-1)) and obtained results that were in excellent agreement with their DFe consensus values: 0.118+/-0.028 nmol L(-1) (n=7) for Surface-1 and 0.932+/-0.059 nmol L(-1) (n=9) for Deep-2. We also present a vertical DFe profile from the western Weddell Sea collected during the <span class="hlt">Ice</span> Station Polarstern (ISPOL) <span class="hlt">ice</span> drift experiment (ANT XXII-2, RV Polarstern) in November 2004-January 2005. The profile shows near-surface DFe concentrations of approximately 0.6 nmol L(-1) and bottom water enrichment up to 23 nmol L(-1) DFe.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19264405','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19264405"><span>A sensor of alcohol <span class="hlt">vapours</span> based on thin polyaniline base film and quartz crystal microbalance.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ayad, Mohamad M; El-Hefnawey, Gad; Torad, Nagy L</p> <p>2009-08-30</p> <p>Thin films of polyaniline base, emeraldine base (EB), coating on the quartz crystal microbalance (QCM) electrode were used as a sensitive layer for the detection of a number of primary aliphatic alcohols such as ethanol, methanol, 2-propanol and 1-propanol <span class="hlt">vapours</span>. The frequency shifts (Deltaf) of the QCM were increased due to the <span class="hlt">vapour</span> adsorption into the EB film. Deltaf were found to be linearly correlated with the concentrations of alcohols <span class="hlt">vapour</span> in part per million (ppm). The sensitivity of the sensor was found to be governed by the chemical structure of the alcohol. The sensor shows a good reproducibility and reversibility. The diffusions of different alcohols <span class="hlt">vapour</span> were studied and the diffusion coefficients (D) were calculated. It is concluded that the diffusion of the <span class="hlt">vapours</span> into the EB film follows Fickian kinetics.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19780024726','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19780024726"><span>The effect of <span class="hlt">seawater</span> on thermoregulator centers</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Dontas, S.; Phocas, E.</p> <p>1978-01-01</p> <p>Experiments were done on dogs to determine the mechanism of thermoregulation. Results show that natural <span class="hlt">seawater</span>, injected intravenously (150, 200, and 300 cc ), causes narcosis of the thermic centers and increases temperature. Diluted <span class="hlt">seawater</span> injection causes an excitation of the thermic centers and an antipyretic effect.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AtmRe.167..108S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AtmRe.167..108S"><span><span class="hlt">Ice</span> crystal precipitation at Dome C site (East Antarctica)</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Santachiara, G.; Belosi, F.; Prodi, F.</p> <p>2016-01-01</p> <p>For the first time, falling <span class="hlt">ice</span> crystals were collected on glass slides covered with a thin layer of 2% formvar in chloroform at the Dome Concordia site (Dome C), Antarctica. Samplings were performed in the framework of the 27th Italian Antarctica expedition of the Italian National Program for Research in Antarctica in the period 21 February-6 August 2012. Events of clear-sky precipitations and precipitations from clouds were considered and the replicas obtained were examined under Scanning Electron Microscope (SEM). Several shapes of <span class="hlt">ice</span> crystals were identified, including ;diamond dust; (plates, pyramids, hollow and solid columns), and crystal aggregates varying in complexity. Single events often contained both small (10 μm to 50 μm) and large (hundreds of microns) crystals, suggesting that crystals can form simultaneously near the ground (height of a few hundred metres) and at higher layers (height of thousands of metres). Images of sampled crystal replicas showed that single bullets are not produced separately, but by the disintegration of combinations of bullets. Rimed <span class="hlt">ice</span> crystals were absent in the Dome C samples, i.e. the only mode of crystal growth was water <span class="hlt">vapour</span> diffusion. On considering the aerosol in the sampled crystals, we reached the conclusion that inertial impaction, interception and Brownian motion were insufficient to explain the scavenged aerosol. We therefore presume that phoretic forces play a role in scavenging during the crystal growth process.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.A53K..02F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.A53K..02F"><span>Contribution of <span class="hlt">Seawater</span> Surfactants to Generated Primary Marine Aerosol Particles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Frossard, A. A.; Gerard, V.; Duplessis, P.; Kinsey, J. D.; Lu, X.; Zhu, Y.; Bisgrove, J.; Maben, J. R.; Long, M. S.; Chang, R.; Beaupre, S. R.; Kieber, D. J.; Keene, W. C.; Noziere, B.; Cohen, R. C.</p> <p>2017-12-01</p> <p>Surfactants account for minor fractions of total organic carbon in the ocean but may have major impacts on the surface tension of bursting bubbles at the sea surface that drive the production of primary marine aerosol particles (PMA). Surfactants associated with marine aerosol may also significantly reduce the surface tension of water thereby increasing the potential for cloud droplet activation and growth. During September and October 2016, PMA were produced from bursting bubbles in <span class="hlt">seawater</span> using a high capacity generator at two biologically productive and two oligotrophic stations in the western North Atlantic, as part of a cruise on the R/V Endeavor. Surfactants were extracted from paired PMA and <span class="hlt">seawater</span> samples, and their ionic compositions, total concentrations, and critical micelle concentrations (CMC) were quantified and compared for the four hydrographic stations. Higher surfactant concentrations were determined in the aerosol produced from biologically productive <span class="hlt">seawater</span> compared to oligotrophic <span class="hlt">seawater</span>, and the surfactants extracted from productive <span class="hlt">seawater</span> were stronger (had lower CMCs) than those in the oligotrophic <span class="hlt">seawater</span>. Surfactants associated with PMA and <span class="hlt">seawater</span> in productive regions also varied over diel cycles, whereas those in the oligotrophic regions did not. This work demonstrates a direct link between surfactants in <span class="hlt">seawater</span> and those in PMA.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_9");'>9</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li class="active"><span>11</span></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_11 --> <div id="page_12" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="221"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.usgs.gov/sir/2009/5028/','USGSPUBS'); return false;" href="https://pubs.usgs.gov/sir/2009/5028/"><span>Application of <span class="hlt">SEAWAT</span> to select variable-density and viscosity problems</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Dausman, Alyssa M.; Langevin, Christian D.; Thorne, Danny T.; Sukop, Michael C.</p> <p>2010-01-01</p> <p><span class="hlt">SEAWAT</span> is a combined version of MODFLOW and MT3DMS, designed to simulate three-dimensional, variable-density, saturated groundwater flow. The most recent version of the <span class="hlt">SEAWAT</span> program, <span class="hlt">SEAWAT</span> Version 4 (or <span class="hlt">SEAWAT</span>_V4), supports equations of state for fluid density and viscosity. In <span class="hlt">SEAWAT</span>_V4, fluid density can be calculated as a function of one or more MT3DMS species, and optionally, fluid pressure. Fluid viscosity is calculated as a function of one or more MT3DMS species, and the program also includes additional functions for representing the dependence of fluid viscosity on temperature. This report documents testing of and experimentation with <span class="hlt">SEAWAT</span>_V4 with six previously published problems that include various combinations of density-dependent flow due to temperature variations and/or concentration variations of one or more species. Some of the problems also include variations in viscosity that result from temperature differences in water and oil. Comparisons between the results of <span class="hlt">SEAWAT</span>_V4 and other published results are generally consistent with one another, with minor differences considered acceptable.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009GeCoA..73.5959G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009GeCoA..73.5959G"><span>Ultra-low rare earth element content in accreted <span class="hlt">ice</span> from sub-glacial Lake Vostok, Antarctica</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gabrielli, Paolo; Planchon, Frederic; Barbante, Carlo; Boutron, Claude F.; Petit, Jean Robert; Bulat, Sergey; Hong, Sungmin; Cozzi, Giulio; Cescon, Paolo</p> <p>2009-10-01</p> <p>This paper reports the first rare earth element (REE) concentrations in accreted <span class="hlt">ice</span> refrozen from sub-glacial Lake Vostok (East Antarctica). REE were determined in various sections of the Vostok <span class="hlt">ice</span> core in order to geochemically characterize its impurities. Samples were obtained from accreted <span class="hlt">ice</span> and, for comparison, from the upper glacier <span class="hlt">ice</span> of atmospheric origin (undisturbed, disturbed and glacial flour <span class="hlt">ice</span>). REE concentrations ranged between 0.8-56 pg g -1 for Ce and 0.0035-0.24 pg g -1 for Lu in glacier <span class="hlt">ice</span>, and between <0.1-24 pg g -1 for Ce and <0.0004-0.02 pg g -1 for Lu in accreted <span class="hlt">ice</span>. Interestingly, the REE concentrations in the upper accreted <span class="hlt">ice</span> (AC 1; characterized by visible aggregates containing a mixture of very fine terrigenous particles) and in the deeper accreted <span class="hlt">ice</span> (AC 2; characterized by transparent <span class="hlt">ice</span>) are lower than those in fresh water and <span class="hlt">seawater</span>, respectively. We suggest that such ultra-low concentrations are unlikely to be representative of the real REE content in Lake Vostok, but instead may reflect phase exclusion processes occurring at the <span class="hlt">ice</span>/water interface during refreezing. In particular, the uneven spatial distribution (on the order of a few cm) and the large range of REE concentrations observed in AC 1 are consistent with the occurrence/absence of the aggregates in adjacent <span class="hlt">ice</span>, and point to the presence of solid-phase concentration/exclusion processes occurring within separate pockets of frazil <span class="hlt">ice</span> during AC 1 formation. Interestingly, if the LREE enrichment found in AC 1 was not produced by chemical fractionation occurring in Lake Vostok water, this may reflect a contribution of bedrock material, possibly in combination with aeolian dust released into the lake by melting of the glacier <span class="hlt">ice</span>. Collectively, this valuable information provides new insight into the accreted <span class="hlt">ice</span> formation processes, the bedrock geology of East Antarctica as well as the water chemistry and circulation of Lake Vostok.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009AGUFM.U53C..12B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009AGUFM.U53C..12B"><span>Ultra-low rare earth element content in accreted <span class="hlt">ice</span> from sub-glacial Lake Vostok, Antarctica</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Barbante, C.; Gabrielli, P.; Turetta, C.; Planchon, F.; Boutron, C.; Petit, J. R.; Bulat, S.; Hong, S.; Cozzi, G.; Cescon, P.</p> <p>2009-12-01</p> <p>We report the first rare earth element (REE) concentrations in accreted <span class="hlt">ice</span> refrozen from sub-glacial Lake Vostok (East Antarctica). REE were determined in various sections of the Vostok <span class="hlt">ice</span> core in order to geochemically characterize its impurities. Samples were obtained from accreted <span class="hlt">ice</span> and, for comparison, from the upper glacier <span class="hlt">ice</span> of atmospheric origin (undisturbed, disturbed and glacial flour <span class="hlt">ice</span>). REE concentrations ranged between 0.8-56 pg g-1 for Ce and 0.0035- 0.24 pg g-1 for Lu in glacier <span class="hlt">ice</span>, and between <0.1-24 pg g-1 for Ce and <0.0004-0.02 pg g-1 for Lu in accreted <span class="hlt">ice</span>. Interestingly, the REE concentrations in the upper accreted <span class="hlt">ice</span> (AC1;characterized by visible aggregates containing a mixture of very fine terrigenous particles) and in the deeper accreted <span class="hlt">ice</span> (AC2; characterized by transparent <span class="hlt">ice</span>) are lower than those in fresh water and <span class="hlt">seawater</span>, respectively. We suggest that such ultra-low concentrations are unlikely to be representative of the real REE content in Lake Vostok, but instead may reflect phase exclusion processes occurring at the <span class="hlt">ice</span>/water interface during refreezing. In particular, the uneven spatial distribution (on the order of a few cm) and the large range of REE concentrations observed in AC1 are consistent with the occurrence/absence of the aggregates in adjacent <span class="hlt">ice</span>, and point to the presence of solid-phase concentration/exclusion processes occurring within separate pockets of frazil <span class="hlt">ice</span> during AC1 formation. Interestingly, if the LREE enrichment found in AC1 was not produced by chemical fractionation occurring in Lake Vostok water, this may reflect a contribution of bedrock material, possibly in combination with aeolian dust released into the lake by melting of the glacier <span class="hlt">ice</span>. Collectively, this valuable information provides new insight into the accreted <span class="hlt">ice</span> formation processes, the bedrock geology of East Antarctica as well as the water chemistry and circulation of Lake Vostok.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.C53B0574L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.C53B0574L"><span><span class="hlt">Ice</span> Shelf-Ocean Interactions Near <span class="hlt">Ice</span> Rises and <span class="hlt">Ice</span> Rumples</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lange, M. A.; Rückamp, M.; Kleiner, T.</p> <p>2013-12-01</p> <p>The stability of <span class="hlt">ice</span> shelves depends on the existence of embayments and is largely influenced by <span class="hlt">ice</span> rises and <span class="hlt">ice</span> rumples, which act as 'pinning-points' for <span class="hlt">ice</span> shelf movement. Of additional critical importance are interactions between <span class="hlt">ice</span> shelves and the water masses underlying them in <span class="hlt">ice</span> shelf cavities, particularly melting and refreezing processes. The present study aims to elucidate the role of <span class="hlt">ice</span> rises and <span class="hlt">ice</span> rumples in the context of climate change impacts on Antarctic <span class="hlt">ice</span> shelves. However, due to their smaller spatial extent, <span class="hlt">ice</span> rumples react more sensitively to climate change than <span class="hlt">ice</span> rises. Different forcings are at work and need to be considered separately as well as synergistically. In order to address these issues, we have decided to deal with the following three issues explicitly: oceanographic-, cryospheric and general topics. In so doing, we paid particular attention to possible interrelationships and feedbacks in a coupled <span class="hlt">ice</span>-shelf-ocean system. With regard to oceanographic issues, we have applied the ocean circulation model ROMBAX to ocean water masses adjacent to and underneath a number of idealized <span class="hlt">ice</span> shelf configurations: wide and narrow as well as laterally restrained and unrestrained <span class="hlt">ice</span> shelves. Simulations were performed with and without small <span class="hlt">ice</span> rises located close to the calving front. For larger configurations, the impact of the <span class="hlt">ice</span> rises on melt rates at the <span class="hlt">ice</span> shelf base is negligible, while for smaller configurations net melting rates at the <span class="hlt">ice</span>-shelf base differ by a factor of up to eight depending on whether <span class="hlt">ice</span> rises are considered or not. We employed the thermo-coupled <span class="hlt">ice</span> flow model TIM-FD3 to simulate the effects of several <span class="hlt">ice</span> rises and one <span class="hlt">ice</span> rumple on the dynamics of <span class="hlt">ice</span> shelf flow. We considered the complete un-grounding of the <span class="hlt">ice</span> shelf in order to investigate the effect of pinning points of different characteristics (interior or near calving front, small and medium sized) on the resulting flow and stress fields</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009SPIE.7508E..0FW','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009SPIE.7508E..0FW"><span>Online PH measurement technique in <span class="hlt">seawater</span> desalination</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wang, Haibo; Wu, Kaihua; Hu, Shaopeng</p> <p>2009-11-01</p> <p>The measurement technology of pH is essential in <span class="hlt">seawater</span> desalination. Glass electrode is the main pH sensor in <span class="hlt">seawater</span> desalination. Because the internal impedance of glass electrode is high and the signal of pH sensor is easy to be disturbed, a signal processing circuit with high input impedance was designed. Because of high salinity of <span class="hlt">seawater</span> and the characteristic of glass electrode, ultrasonic cleaning technology was used to online clean pH sensor. Temperature compensation was also designed to reduce the measurement error caused by variety of environment temperature. Additionally, the potential drift of pH sensor was analyzed and an automatic calibration method was proposed. In order to online monitor the variety of pH in <span class="hlt">seawater</span> desalination, three operating modes were designed. The three modes are online monitoring mode, ultrasonic cleaning mode and auto-calibration mode. The current pH in <span class="hlt">seawater</span> desalination was measured and displayed in online monitoring mode. The cleaning process of pH sensor was done in ultrasonic cleaning mode. The calibration of pH sensor was finished in auto-calibration mode. The result of experiments showed that the measurement technology of pH could meet the technical requirements for desalination. The glass electrode could be promptly and online cleaned and its service life was lengthened greatly.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007AIPC..909..210S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007AIPC..909..210S"><span>Inhibition of Sodium Benzoate on Stainless Steel in Tropical <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Seoh, S. Y.; Senin, H. B.; Nik, W. N. Wan; Amin, M. M.</p> <p>2007-05-01</p> <p>The inhibition of sodium benzoate for stainless steel controlling corrosion was studied in <span class="hlt">seawater</span> at room temperature. Three sets of sample have been immersed in <span class="hlt">seawater</span> containing sodium benzoate with the concentrations of 0.3M, 0.6M and 1.0M respectively. One set of sample has been immersed in <span class="hlt">seawater</span> without adding any sodium benzoate. It was found that the highest corrosion rate was observed for the stainless steel with no inhibitor was added to the <span class="hlt">seawater</span>. As the concentration of sodium benzoate being increased, the corrosion rate is decreases. Results show that by the addition of 1.0M of sodium benzoate in <span class="hlt">seawater</span> samples, it giving ≥ 90% efficiencies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017PalOc..32.1195V','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017PalOc..32.1195V"><span>Timing of Deglacial AMOC Variability From a High-Resolution <span class="hlt">Seawater</span> Cadmium Reconstruction</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Valley, Shannon; Lynch-Stieglitz, Jean; Marchitto, Thomas M.</p> <p>2017-11-01</p> <p>A new, high-resolution record of benthic <span class="hlt">seawater</span> Cd (Cdw) was generated from a Florida Straits sediment core at 546 m water depth. The record provides additional evidence for Cdw below modern values in this channel during the Younger Dryas and Heinrich Stadial 1—climatological periods associated with <span class="hlt">ice</span> sheet melt. Lower Cdw values are interpreted as a weakening of the Atlantic Meridional Overturning Circulation (AMOC), reflecting a decreased northward transport of southern sourced higher-nutrient intermediate waters by the surface return flow of AMOC. Comparison of this new Cdw record with previously published neodymium isotope and δ18O records from the same core shows synchronous transitions, further illustrating the connection between Cdw levels and AMOC strength in the Florida Straits. An increase in Cdw near 16 ka bolsters existing evidence for a resumption of upper branch AMOC strength approximately midway through Heinrich Stadial 1.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24269798','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24269798"><span>Concentration of enteric virus indicator from <span class="hlt">seawater</span> using granular activated carbon.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cormier, Jiemin; Gutierrez, Miguel; Goodridge, Lawrence; Janes, Marlene</p> <p>2014-02-01</p> <p>Fecal contamination of shellfish growing <span class="hlt">seawater</span> with enteric viruses is often associated with human outbreaks of gastroenteritis. Male specific bacteriophage MS2 is correlated with those of enteric viruses in a wide range of water environments and has been used widely as a surrogate for pathogenic waterborne viruses. Since viruses in contaminated water are usually at low levels, the development of methods to concentrate viruses from water is crucial for detection purposes. In the present study, granular activated carbon was evaluated for concentration of MS2 from artificial <span class="hlt">seawater</span>, and different parameters of the <span class="hlt">seawater</span> were also compared. Recovery of MS2 from warm <span class="hlt">seawater</span> (37°C) was found to be significantly greater than from cold <span class="hlt">seawater</span> (4 and 20°C), and even greater than from fresh water (4, 20 and 37°C); the difference between <span class="hlt">seawater</span> and fresh water became less profound when the temperatures of both were below 37°C. Although not of statistical significance, recovery of MS2 from low salinity <span class="hlt">seawater</span> (10 and 20 parts per thousand, ppt) was greater than from high salinity <span class="hlt">seawater</span> (30 and 40ppt). One gram of granular activated carbon was able to extract 6-log plaque forming units (PFU) of MS2 from 500ml <span class="hlt">seawater</span> at 37°C. This study demonstrated that granular activated carbon can concentrate an enteric virus indicator from shellfish growing <span class="hlt">seawater</span> effectively. Copyright © 2013 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C41E..02A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C41E..02A"><span>Marine <span class="hlt">Ice</span> Crevassing Imaged with Side-looking GPR: Implications for Stability within the McMurdo Shear Zone</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Arcone, S. A.; Ray, L.; Lever, J.; Koons, P. O.; Kaluzienski, L. M.</p> <p>2017-12-01</p> <p>Shearing along <span class="hlt">ice</span> shelf margins threatens shelf stability if crevassing results throughout the <span class="hlt">ice</span>. We are investigating a 28 km2 section of the McMurdo Shear Zone (MSZ), which lies between the Ross <span class="hlt">Ice</span> Shelf (RIS) and the McMurdo <span class="hlt">Ice</span> Shelf (MIS). Our gridded transects are east-west, <span class="hlt">ice</span> flow is nearly due north and the RIS compresses against the MIS from east to west. We find nearly synchronized firn and marine <span class="hlt">ice</span> crevassing; the marine <span class="hlt">ice</span> is stratified. However, the lack of any radar evidence for crevassing or fracture within the intermediate 120 m of meteoric <span class="hlt">ice</span> is so far, enigmatic. The marine <span class="hlt">ice</span> crevassing is interpreted from ground-penetrating radar (GPR) trace signatures within 100 m swaths of the interface between the meteoric and marine <span class="hlt">ice</span>; thus the GPR performs like side-looking radar. Symmetric and deformed diffraction hyperbolas indicate crevasses oriented at 43-76 degrees relative to <span class="hlt">ice</span> flow, as seen in the firn. Those near 45 degrees are interpreted as recently formed while those at greater angles are likely older and rotated. Many traces indicate crevasse warping, lateral faulting, and down-faulting. Traces nearly perpendicular to flow indicate possible wing cracks that grew from the tips of crevasses into the direction of compression from the RIS. We interpret the marine crevasses to have originated at the meteoric-marine interface, and to have extended to the shelf bottom because they appear filled with unstratified frozen <span class="hlt">seawater</span>. In view of these observations, and that the intermediate meteoric <span class="hlt">ice</span> must be under similar although not exactly the same stresses, the lack of fracturing within the meteoric <span class="hlt">ice</span> may imply that suturing following brittle and ductile shear deformation provides stability for the MSZ and may result from this east-west compression of the RIS against the MIS.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AMT....10.2851W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AMT....10.2851W"><span>Intercomparison of atmospheric water <span class="hlt">vapour</span> measurements at a Canadian High Arctic site</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Weaver, Dan; Strong, Kimberly; Schneider, Matthias; Rowe, Penny M.; Sioris, Chris; Walker, Kaley A.; Mariani, Zen; Uttal, Taneil; McElroy, C. Thomas; Vömel, Holger; Spassiani, Alessio; Drummond, James R.</p> <p>2017-08-01</p> <p>Water <span class="hlt">vapour</span> is a critical component of the Earth system. Techniques to acquire and improve measurements of atmospheric water <span class="hlt">vapour</span> and its isotopes are under active development. This work presents a detailed intercomparison of water <span class="hlt">vapour</span> total column measurements taken between 2006 and 2014 at a Canadian High Arctic research site (Eureka, Nunavut). Instruments include radiosondes, sun photometers, a microwave radiometer, and emission and solar absorption Fourier transform infrared (FTIR) spectrometers. Close agreement is observed between all combination of datasets, with mean differences ≤ 1.0 kg m-2 and correlation coefficients ≥ 0.98. The one exception in the observed high correlation is the comparison between the microwave radiometer and a radiosonde product, which had a correlation coefficient of 0.92.A variety of biases affecting Eureka instruments are revealed and discussed. A subset of Eureka radiosonde measurements was processed by the Global Climate Observing System (GCOS) Reference Upper Air Network (GRUAN) for this study. Comparisons reveal a small dry bias in the standard radiosonde measurement water <span class="hlt">vapour</span> total columns of approximately 4 %. A recently produced solar absorption FTIR spectrometer dataset resulting from the MUSICA (MUlti-platform remote Sensing of Isotopologues for investigating the Cycle of Atmospheric water) retrieval technique is shown to offer accurate measurements of water <span class="hlt">vapour</span> total columns (e.g. average agreement within -5.2 % of GRUAN and -6.5 % of a co-located emission FTIR spectrometer). However, comparisons show a small wet bias of approximately 6 % at the high-latitude Eureka site. In addition, a new dataset derived from Atmospheric Emitted Radiance Interferometer (AERI) measurements is shown to provide accurate water <span class="hlt">vapour</span> measurements (e.g. average agreement was within 4 % of GRUAN), which usefully enables measurements to be taken during day and night (especially valuable during polar night).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPhCS.891a2123S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPhCS.891a2123S"><span>The Droplets Condensate Centering in the <span class="hlt">Vapour</span> Channel of Short Low Temperature Heat Pipes at High Heat Loads</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Seryakov, A. V.; Shakshin, S. L.; Alekseev, A. P.</p> <p>2017-11-01</p> <p>The results of experimental studies of the process of condensate microdroplets centering contained in the moving moist <span class="hlt">vapour</span> in the <span class="hlt">vapour</span> channel of short heat pipes (HPs) for large thermal loads are presented. A <span class="hlt">vapour</span> channel formed by capillary-porous insert in the form of the inner Laval-liked nozzle along the entire length of the HP. In the upper cover forming a condensation surface in the HP, on the diametrical line are installed capacitive sensors, forming three capacitors located at different distances from the longitudinal axis of the <span class="hlt">vapour</span> channel. With increasing heat load and the boil beginning in the evaporator a large amount of moist <span class="hlt">vapour</span> in the <span class="hlt">vapour</span> channel of HP occur the pressure pulsation with frequency of 400-500 Hz and amplitude up to 1·104Pa. These pulsations affect the moving of the inertial droplets subsystem of the <span class="hlt">vapour</span> and due to the heterogeneity of the velocity profile around the particle flow in the <span class="hlt">vapour</span> channel at the diameter of microdroplets occurs transverse force, called the Saffman force and shear microdroplets to the center of <span class="hlt">vapour</span> channel. Using installed in the top cover capacitors we can record the radial displacement of the condensable microdroplets.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19362188','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19362188"><span>Alcohol <span class="hlt">vapours</span> sensor based on thin polyaniline salt film and quartz crystal microbalance.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ayad, Mohamad M; Torad, Nagy L</p> <p>2009-06-15</p> <p>A sensor based on the quartz crystal microbalance (QCM) technique was developed for detection of a number of primary aliphatic alcohols such as ethanol, methanol, 1-propanol, and 2-propanol <span class="hlt">vapours</span>. Detection was based on a sensitive and a thin film of polyaniline, emeraldine salt (ES), coated the QCM electrode. The frequency shifts (Delta f) of the QCM were increased due to the <span class="hlt">vapour</span> absorption into the ES film. The values of Delta f were found to be linearly correlated with the concentrations of alcohols <span class="hlt">vapour</span> in mg L(-1). The changes in frequency are due to the hydrophilic character of the ES and the electrostatic interaction as well as the type of the alcohol. The sensor shows a good reproducibility and reversibility. The diffusion and diffusion coefficient (D) of different alcohols <span class="hlt">vapour</span> were determined. It was found that the sensor follows Fickian kinetics.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=refrigeration&pg=5&id=EJ093453','ERIC'); return false;" href="https://eric.ed.gov/?q=refrigeration&pg=5&id=EJ093453"><span>Saturated <span class="hlt">Vapour</span> Pressure and Refrigeration - Part I</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Bunker, C. A.</p> <p>1973-01-01</p> <p>The first part of a two-part article describes an experimental approach that can be used in teaching the concept of saturated <span class="hlt">vapour</span> pressure. This leads to a discussion of refrigeration cycles in the second part of the article. (JR)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28898854','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28898854"><span>Factors affecting <span class="hlt">seawater</span>-based pretreatment of lignocellulosic date palm residues.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Fang, Chuanji; Thomsen, Mette Hedegaard; Frankær, Christian Grundahl; Bastidas-Oyanedel, Juan-Rodrigo; Brudecki, Grzegorz P; Schmidt, Jens Ejbye</p> <p>2017-12-01</p> <p><span class="hlt">Seawater</span>-based pretreatment of lignocellulosic biomass is an innovative process at research stage. With respect to process optimization, factors affecting <span class="hlt">seawater</span>-based pretreatment of lignocellulosic date palm residues were studied for the first time in this paper. Pretreatment temperature (180°C-210°C), salinity of <span class="hlt">seawater</span> (0ppt-50ppt), and catalysts (H 2 SO 4 , Na 2 CO 3 , and NaOH) were investigated. The results showed that pretreatment temperature exerted the largest influence on <span class="hlt">seawater</span>-based pretreatment in terms of the enzymatic digestibility and fermentability of pretreated solids, and the inhibition of pretreatment liquids to Saccharomyces cerevisiae. Salinity showed the least impact to <span class="hlt">seawater</span>-based pretreatment, which widens the application spectrum of saline water sources such as brines discharged in desalination plant. Sulfuric acid was the most effective catalyst for <span class="hlt">seawater</span>-based pretreatment compared with Na 2 CO 3 and NaOH. Copyright © 2017 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015EGUGA..17.9347R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015EGUGA..17.9347R"><span>Nucleation from <span class="hlt">seawater</span> emissions during mesocosm experiments</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Rose, Clémence; Culot, Anais; Pey, Jorge; Schwier, Allison; Mas, Sébastien; Charriere, Bruno; Sempéré, Richard; Marchand, Nicolas; D'Anna, Barbara; Sellegri, Karine</p> <p>2015-04-01</p> <p>Nucleation and new particle formation in the marine atmosphere is usually associated to the presence of macroalgea emerged at low tides in coastal areas, while these processes were very rarely detected away from coastlines. In the present study, we evidence the formation of new particles from the 1 nm size above the <span class="hlt">seawater</span> surface in the absence of any macroalgea population. Within the SAM project (Sources of marine Aerosol in the Mediterranean),<span class="hlt">seawater</span> mesocosms experiments were deployed in May 2013 at the STARESO in western Corsica, with the goal of investigating the relationship between marine aerosol emissions and the <span class="hlt">seawater</span> biogeochemical properties. Three mesocosms imprisoned 3,3 m3 of <span class="hlt">seawater</span> each and their emerged part was flushed with aerosol-filtered natural air. One of these mesocosms was left unchanged as control and the two others were enriched by addition of nitrates and phosphates respecting Redfield ratio (N:P = 16) in order to create different levels of phytoplanctonic activities. We followed both water and air characteristics of three mesocosms during a period of three weeks by using online water and atmospheric probes as well as <span class="hlt">seawater</span> daily samples for chemical and biological analysis. Secondary new particle formation was followed on-line in the emerged parts of the mesocosms, using a SMPS for the size distribution above 6 nm and a Particle Size Magnifyer (PSM) for the number of cluster particles between 1 and 6 nm. We will present how the cluster formation rates and early growth rates relate to the gaz-phase emissions from the <span class="hlt">seawater</span> and to its biogeochemical properties. Aknowledgemnts: The authors want to acknowledge the financial support of the ANR "Source of marine Aerosol in the Mediterranean" (SAM), and the support of MISTRAL CHARMEX and MERMEX programs.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29474091','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29474091"><span>Photodegradation of Dicloran in Freshwater and <span class="hlt">Seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Vebrosky, Emily N; Saranjampour, Parichehr; Crosby, Donald G; Armbrust, Kevin L</p> <p>2018-03-21</p> <p>Dicloran appears to be a model pesticide for investigating photodegradation processes in surface waters. Photodegradation processes are particularly relevant to this compound as it is applied to crops grown in proximity to freshwater and marine ecosystems. The photodegradation of dicloran under simulated sunlight was measured in distilled water, artificial <span class="hlt">seawater</span>, phosphate buffer, and filter-sterilized estuarine water to determine its half-life, degradation rate, and photodegradation products. The half-life was approximately 7.5 h in all media. There was no significant difference in the rate of degradation between distilled water and artificial <span class="hlt">seawater</span> for dicloran. For the intermediate products, a higher concentration of 2-chloro-1,4-benzoquinone was measured in artificial <span class="hlt">seawater</span> versus distilled water, while a slightly higher concentration of 1,4-benzoquinone was measured in distilled water versus artificial <span class="hlt">seawater</span>. The detection of chloride and nitrate ions after 2 h of light exposure suggests photonucleophilic substitution contributes to the degradation process. Differences in product distributions between water types suggest that salinity impacts on chemical degradation may need to be addressed in chemical exposure assessments.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2001ApSS..182...49H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2001ApSS..182...49H"><span>Kinetic studies of BTEX <span class="hlt">vapour</span> adsorption onto surfaces of calix-4-resorcinarene films</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hassan, A. K.; Ray, A. K.; Nabok, A. V.; Wilkop, T.</p> <p>2001-10-01</p> <p>The exposure of spun films of an amphiphilic calix-4-resorcinarene (C-4-RA) derivative to <span class="hlt">vapours</span> of benzene, toluene, ethylbenzene, and m-xylene (BTEX) has produced a graded response, promising for the development of multisensor arrays. Fast and reversible adsorption of ethylbenzene was associated with changing the refractive index of the sensing layer and is believed to be due to the host-guest interaction between the cavitand C-4-RA molecules and the <span class="hlt">vapour</span> molecules. Prolonged irradiation of the films with a focused laser beam has resulted in an initial increase of film sensitivity to the different organic <span class="hlt">vapours</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27493149','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27493149"><span>Microbiome Composition and Diversity of the <span class="hlt">Ice</span>-Dwelling Sea Anemone, Edwardsiella andrillae.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Murray, Alison E; Rack, Frank R; Zook, Robert; Williams, Michael J M; Higham, Mary L; Broe, Michael; Kaufmann, Ronald S; Daly, Marymegan</p> <p>2016-10-01</p> <p>Edwardsiella andrillae is a sea anemone (Cnidaria: Anthozoa: Actiniaria) only known to live embedded in the <span class="hlt">ice</span> at the <span class="hlt">seawater</span> interface on the underside of the Ross <span class="hlt">Ice</span> Shelf, Antarctica. Although the anatomy and morphological characteristics of E. andrillae have been described, the adaptations of this species to the under-<span class="hlt">ice</span> ecosystem have yet to be examined. One feature that may be important to the physiology and ecology of E. andrillae is its microbiome, which may play a role in health and survival, as has been deduced in other metazoans, including anthozoans. Here we describe the microbiome of five specimens of E. andrillae, compare the diversity we recovered to that known for temperate anemones and another Antarctic cnidarian, and consider the phylogenetic and functional implications of microbial diversity for these animals. The E. andrillae microbiome was relatively low in diversity, with seven phyla detected, yet included substantial phylogenetic novelty. Among the five anemones investigated, the distribution of microbial taxa varied; this trait appears to be shared by many anthozoans. Most importantly, specimens either appeared to be dominated by Proteobacteria-affiliated members or by deeply branching Tenericute sequences. There were few closely related sequence types that were common to temperate and Antarctic sea anemone microbiomes, the exception being an Acinetobacter-related representative. Similar observations were made between microbes associated with E. andrillae and an Antarctic soft coral; however, there were several closely-related, low abundance Gammaproteobacteria in both Antarctic microbiomes, particularly from the soft coral, that are also commonly detected in Southern Ocean <span class="hlt">seawater</span>. Although this preliminary study leaves open many questions concerning microbiome diversity and its role in host ecology, we identify major lineages of microbes (e.g., diverse deep-branching Alphaproteobacteria, Epsilonproteobacteria, and divergent</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009ACPD....923271S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009ACPD....923271S"><span>An aerosol chamber investigation of the heterogeneous <span class="hlt">ice</span> nucleating potential of refractory nanoparticles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Saunders, R. W.; Möhler, O.; Schnaiter, M.; Benz, S.; Wagner, R.; Saathoff, H.; Connolly, P. J.; Burgess, R.; Gallagher, M.; Wills, R.; Murray, B. J.; Plane, J. M. C.</p> <p>2009-11-01</p> <p>Nanoparticles of iron oxide (crystalline and amorphous), silicon oxide and magnesium oxide were investigated for their propensity to nucleate <span class="hlt">ice</span> over the temperature range 180-250 K, using the AIDA chamber in Karlsruhe, Germany. All samples were observed to initiate <span class="hlt">ice</span> formation via the deposition mode at threshold <span class="hlt">ice</span> super-saturations (RHi thresh) ranging from 105% to 140% for temperatures below 220 K. Approximately 10% of amorphous Fe2O3 particles (modal diameter = 30 nm) generated in situ from a photochemical aerosol reactor, led to <span class="hlt">ice</span> nucleation at RHi thresh = 140% at an initial chamber temperature of 182 K. Quantitative analysis using a singular hypothesis treatment provided a fitted function [ns (190 K) = 10(3.33×sice)+8.16] for the variation in <span class="hlt">ice</span>-active surface site density (ns: m-2) with <span class="hlt">ice</span> saturation (sice) for Fe2O3 nanoparticles. This was implemented in an aerosol-cloud model to determine a predicted deposition (mass accommodation) coefficient for water <span class="hlt">vapour</span> on <span class="hlt">ice</span> of 0.1 at temperatures appropriate for the upper atmosphere. Classical nucleation theory was used to determine representative contact angles (θ) for the different particle compositions. For the in situ generated Fe2O3 particles, a slight inverse temperature dependence was observed with θ = 10.5° at 182 K, decreasing to 9.0° at 200 K (compared with 10.2° and 11.4°, respectively for the SiO2 and MgO particle samples at the higher temperature). These observations indicate that such refractory nanoparticles are relatively efficient materials for the nucleation of <span class="hlt">ice</span> under the conditions studied in the chamber which correspond to cirrus cloud formation in the upper troposphere. The results also show that Fe2O3 particles do not act as <span class="hlt">ice</span> nuclei under conditions pertinent for tropospheric mixed phase clouds, which necessarily form above ~233 K. At the lower temperatures (<150 K) where noctilucent clouds form during summer months in the high latitude mesosphere, higher contact</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010ACP....10.1227S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010ACP....10.1227S"><span>An aerosol chamber investigation of the heterogeneous <span class="hlt">ice</span> nucleating potential of refractory nanoparticles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Saunders, R. W.; Möhler, O.; Schnaiter, M.; Benz, S.; Wagner, R.; Saathoff, H.; Connolly, P. J.; Burgess, R.; Murray, B. J.; Gallagher, M.; Wills, R.; Plane, J. M. C.</p> <p>2010-02-01</p> <p>Nanoparticles of iron oxide (crystalline and amorphous), silicon oxide and magnesium oxide were investigated for their propensity to nucleate <span class="hlt">ice</span> over the temperature range 180-250 K, using the AIDA chamber in Karlsruhe, Germany. All samples were observed to initiate <span class="hlt">ice</span> formation via the deposition mode at threshold <span class="hlt">ice</span> super-saturations (RHithresh) ranging from 105% to 140% for temperatures below 220 K. Approximately 10% of amorphous Fe2O3 particles (modal diameter = 30 nm) generated in situ from a photochemical aerosol reactor, led to <span class="hlt">ice</span> nucleation at RHithresh = 140% at an initial chamber temperature of 182 K. Quantitative analysis using a singular hypothesis treatment provided a fitted function [ns(190 K)=10(3.33×sice)+8.16] for the variation in <span class="hlt">ice</span>-active surface site density (ns:m-2) with <span class="hlt">ice</span> saturation (sice) for Fe2O3 nanoparticles. This was implemented in an aerosol-cloud model to determine a predicted deposition (mass accommodation) coefficient for water <span class="hlt">vapour</span> on <span class="hlt">ice</span> of 0.1 at temperatures appropriate for the upper atmosphere. Classical nucleation theory was used to determine representative contact angles (θ) for the different particle compositions. For the in situ generated Fe2O3 particles, a slight inverse temperature dependence was observed with θ = 10.5° at 182 K, decreasing to 9.0° at 200 K (compared with 10.2° and 11.4° respectively for the SiO2 and MgO particle samples at the higher temperature). These observations indicate that such refractory nanoparticles are relatively efficient materials for the nucleation of <span class="hlt">ice</span> under the conditions studied in the chamber which correspond to cirrus cloud formation in the upper troposphere. The results also show that Fe2O3 particles do not act as <span class="hlt">ice</span> nuclei under conditions pertinent for tropospheric mixed phase clouds, which necessarily form above ~233 K. At the lower temperatures (<150 K) where noctilucent clouds form during summer months in the high latitude mesosphere, higher contact angles would</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_10");'>10</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li class="active"><span>12</span></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_12 --> <div id="page_13" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="241"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMPP51D2333Q','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMPP51D2333Q"><span>Constraining past <span class="hlt">seawater</span> δ18O and temperature records developed from foraminiferal geochemistry</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Quinn, T. M.; Thirumalai, K.; Marino, G.</p> <p>2016-12-01</p> <p>Paired measurements of magnesium-to-calcium ratios (Mg/Ca) and the stable oxygen isotopic composition (δ18O) in foraminifera have significantly advanced our knowledge of the climate system by providing information on past temperature and <span class="hlt">seawater</span> δ18O (δ18Osw, a proxy for salinity and <span class="hlt">ice</span> volume). However, multiple sources of uncertainty exist in transferring these downcore geochemical data into quantitative paleoclimate reconstructions. Here, we develop a computational toolkit entitled Paleo-<span class="hlt">Seawater</span> Uncertainty Solver (PSU Solver) that performs bootstrap Monte Carlo simulations to constrain these various sources of uncertainty. PSU Solver calculates temperature and δ18Osw, and their respective confidence intervals using an iterative approach with user-defined errors, calibrations, and sea-level curves. Our probabilistic approach yields reduced uncertainty constraints compared to theoretical considerations and commonly used propagation exercises. We demonstrate the applicability of PSU Solver for published records covering three timescales: the late Holocene, the last deglaciation, and the last glacial period. We show that the influence of salinity on Mg/Ca can considerably alter the structure and amplitude of change in the resulting reconstruction and can impact the interpretation of paleoceanographic time series. We also highlight the sensitivity of the records to various inputs of sea-level curves, transfer functions, and uncertainty constraints. PSU Solver offers an expeditious yet rigorous approach to test the robustness of past climate variability inferred from paired Mg/Ca-δ18O measurements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4917840','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4917840"><span>Aerosol assisted chemical <span class="hlt">vapour</span> deposition of gas sensitive SnO2 and Au-functionalised SnO2 nanorods via a non-catalysed <span class="hlt">vapour</span> solid (VS) mechanism</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Vallejos, Stella; Selina, Soultana; Annanouch, Fatima Ezahra; Gràcia, Isabel; Llobet, Eduard; Blackman, Chris</p> <p>2016-01-01</p> <p>Tin oxide nanorods (NRs) are <span class="hlt">vapour</span> synthesised at relatively lower temperatures than previously reported and without the need for substrate pre-treatment, via a <span class="hlt">vapour</span>-solid mechanism enabled using an aerosol-assisted chemical <span class="hlt">vapour</span> deposition method. Results demonstrate that the growth of SnO2 NRs is promoted by a compression of the nucleation rate parallel to the substrate and a decrease of the energy barrier for growth perpendicular to the substrate, which are controlled via the deposition conditions. This method provides both single-step formation of the SnO2 NRs and their integration with silicon micromachined platforms, but also allows for in-situ functionalization of the NRs with gold nanoparticles via co-deposition with a gold precursor. The functional properties are demonstrated for gas sensing, with microsensors using functionalised NRs demonstrating enhanced sensing properties towards H2 compared to those based on non-functionalised NRs. PMID:27334232</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24241776','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24241776"><span>Environmental impact of <span class="hlt">seawater</span> desalination plants.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Al-Mutaz, I S</p> <p>1991-01-01</p> <p>Enormous amounts of <span class="hlt">seawater</span> are desalted everyday worldwide. The total world production of fresh water from the sea is about 2621 mgd (9.92 million m(3) day(-1) 1985 figures). Desalting processes are normally associated with the rejection of high concentration waste brine from the plant itself or from the pretreatment units as well as during the cleaning period. In thermal processes, mainly multistage flash (MSF) thermal pollution occurs. These pollutants increase the <span class="hlt">seawater</span> temperature, salinity, water current and turbidity. They also harm the marine environment, causing fish to migrate while enhancing the presence of algae, nematods and tiny molluscus. Sometimes micro-elements and toxic materials appear in the discharged brine.This paper will discuss the impact of the effluents from the desalination plants on the <span class="hlt">seawater</span> environment with particular reference to the Saudi desalination plants, since they account for about 50% of the world desalination capacity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70169889','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70169889"><span>Tracking millennial-scale Holocene glacial advance and retreat using osmium isotopes: Insights from the Greenland <span class="hlt">ice</span> sheet</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Rooney, Alan D.; Selby, David; Llyod, Jeremy M.; Roberts, David H.; Luckge, Andreas; Sageman, Bradley B.; Prouty, Nancy G.</p> <p>2016-01-01</p> <p>High-resolution Os isotope stratigraphy can aid in reconstructing Pleistocene <span class="hlt">ice</span> sheet fluctuation and elucidating the role of local and regional weathering fluxes on the marine Os residence time. This paper presents new Os isotope data from ocean cores adjacent to the West Greenland <span class="hlt">ice</span> sheet that have excellent chronological controls. Cores MSM-520 and DA00-06 represent distal to proximal sites adjacent to two West Greenland <span class="hlt">ice</span> streams. Core MSM-520 has a steadily decreasing Os signal over the last 10 kyr (187Os/188Os = 1.35–0.81). In contrast, Os isotopes from core DA00-06 (proximal to the calving front of Jakobshavn Isbræ) highlight four stages of <span class="hlt">ice</span> stream retreat and advance over the past 10 kyr (187Os/188Os = 2.31; 1.68; 2.09; 1.47). Our high-resolution chemostratigraphic records provide vital benchmarks for <span class="hlt">ice</span>-sheet modelers as we attempt to better constrain the future response of major <span class="hlt">ice</span> sheets to climate change. Variations in Os isotope composition from sediment and macro-algae (seaweed) sourced from regional and global settings serve to emphasize the overwhelming effect weathering sources have on <span class="hlt">seawater</span> Os isotope composition. Further, these findings demonstrate that the residence time of Os is shorter than previous estimates of ∼104 yr.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2003PCE....28.1273G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2003PCE....28.1273G"><span>Extremophilic fungi in arctic <span class="hlt">ice</span>: a relationship between adaptation to low temperature and water activity</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gunde-Cimerman, N.; Sonjak, S.; Zalar, P.; Frisvad, J. C.; Diderichsen, B.; Plemenitaš, A.</p> <p></p> <p>Little is known about fungal diversity in extremely cold regions. Low temperatures induce the formation of <span class="hlt">ice</span> crystals and therefore also the creation of low water activity ( aw). These are the dominant factors in external chemistry that influence microbial biota in cold regions. Therefore, we have used selective low water activity media plus low incubation temperatures for the isolation of fungi from an Arctic environment. In comparison with the highest values of colony forming units (CFU) obtained on mesophilic media, considerably higher fungal CFU per litre of water were detected on low aw media, ranging from 1000 to 3000 l -1 in <span class="hlt">seawater</span>, 6000 to 7000 l -1 in melted sea <span class="hlt">ice</span> and up to 13,000 l -1 in melted glacier <span class="hlt">ice</span>. The dominant taxa were ascomycetous and basidiomycetous yeasts, melanized fungi, mainly represented by the genera Cladosporium and Aureobasidium plus different species of the genus Penicillium. Preliminary taxonomic analyses revealed several new species and varieties. Further characterisations are needed to determine whether this diversity is due to geographic isolation, ecological conditions or independent evolutionary origin.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017MS%26E..176a2039N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017MS%26E..176a2039N"><span>Impurities Removal in <span class="hlt">Seawater</span> to Optimize the Magnesium Extraction</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Natasha, N. C.; Firdiyono, F.; Sulistiyono, E.</p> <p>2017-02-01</p> <p>Magnesium extraction from <span class="hlt">seawater</span> is promising way because magnesium is the second abundant element in <span class="hlt">seawater</span> and Indonesia has the second longest coastline in the world. To optimize the magnesium extraction, the impurities in <span class="hlt">seawater</span> need to be eliminated. Evaporation and dissolving process were used in this research to remove the impurities especially calcium in <span class="hlt">seawater</span>. <span class="hlt">Seawater</span> which has been evaporated from 100 ml to 50 ml was dissolved with variations solution such as oxalic acid and ammonium bicarbonate. The solution concentration is 100 g/l and it variations are 2 ml, 4 ml, 6 ml, 8 ml, 10 ml, 20 ml, 30 ml, 40 ml and 50 ml. This step will produce precipitate and filtrate then it will be analysed to find out the result of this process. The precipitate was analysed by X-ray Diffraction (XRD) and Scanning Electron Microscope (SEM) but the filtrate was analysed by Inductively Coupled Plasma (ICP). XRD analysis shows that calcium oxalate and calcium carbonate were formed and ICP analysis shows that the remaining calcium in <span class="hlt">seawater</span> using oxalic acid is about 0.01% and sodium 0.14% but when using ammonium bicarbonate the remaining calcium is 2.5% and sodium still more than 90%. The results show that both oxalic acid and ammonium bicarbonate can remove the impurities but when using oxalic acid, not only the impurities but also magnesium was precipitated. The conclusion of this research is the best solution to remove the impurities in <span class="hlt">seawater</span> without precipitate the magnesium is using ammonium bicarbonate.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/1003721','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/1003721"><span>Sporulation and survival of Toxoplasma gondii oocysts in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Lindsay, D.S.; Collins, M.V.; Mitchell, S.M.; Cole, Rebecca A.; Flick, G.J.; Wetch, C.N.; Lindquist, A.; Dubey, J.P.</p> <p>2003-01-01</p> <p>We have been collaborating since 1992 in studies on southern sea otters (Enhdyra lutris nereis) as part of a program to define factors, which may be responsible for limiting the growth of the southern sea otter population. We previously demonstrated Toxoplasma gondii in sea otiers. We postulated that cat feces containing oocysts could be entering the marine environment through storm run-off or through municipal sewage since cat feces are often disposed down toilets by cat owners. The present study examined the sporulation of T. gondiioocysts in <span class="hlt">seawater</span> and the survival of sporulated oocysts in <span class="hlt">seawater</span>. Unsporulated oocysts were placed in 1.5 ppt artificial <span class="hlt">seawater</span>, 32 ppt artificial <span class="hlt">seawater</span> or 2% sulfuric acid (positive control) at 24 C in an incubator. Samples were examined daily for 3 days and development monitored by counting 100 oocysts from each sample. From 75 to 80% of the oocysts were sporulated by 3 days post-inoculation under all treatment conditions. Groups of 2 mice were fed 10,000 oocysts each from each of the 3 treatment groups. All inoculated mice developed toxoplasmosis indicating that oocysts were capable of sporulating in <span class="hlt">seawater</span>. Survival of sporulated oocysts was examined by placing sporulated T. gondii oocysts in 15 ppt <span class="hlt">seawater</span> at room temperature 22–24 C (RT) or in a refrigerator kept at 4 C. Mice fed oocysts that had been stored at 4C or RT for 6 months became infected. These results indicate that T. gondii oocysts can sporulate and remain viable in <span class="hlt">seawater</span> for several months.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1990GeCoA..54.2645B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1990GeCoA..54.2645B"><span>Rare earth element scavenging in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Byrne, Robert H.; Kim, Ki-Hyun</p> <p>1990-10-01</p> <p>Examinations of rare earth element (REE) adsorption in <span class="hlt">seawater</span>, using a variety of surface-types, indicated that, for most surfaces, light rare earth elements (LREEs) are preferentially adsorbed compared to the heavy rare earths (HREEs). Exceptions to this behavior were observed only for silica phases (glass surfaces, acid-cleaned diatomaceous earth, and synthetic SiO 2). The affinity of the rare earths for surfaces can be strongly affected by thin organic coatings. Glass surfaces which acquired an organic coating through immersion in Tampa Bay exhibited adsorptive behavior typical of organic-rich, rather than glass, surfaces. Models of rare earth distributions between <span class="hlt">seawater</span> and carboxylate-rich surfaces indicate that scavenging processes which involve such surfaces should exhibit a strong dependence on pH and carbonate complexation. Scavenging models involving carboxylate surfaces produce relative REE abundance patterns in good general agreement with observed shale-normalized REE abundances in <span class="hlt">seawater</span>. Scavenging by carboxylate-rich surfaces should produce HREE enrichments in <span class="hlt">seawater</span> relative to the LREEs and may produce enrichments of lanthanum relative to its immediate trivalent neighbors. Due to the origin of distribution coefficients as a difference between REE solution complexation (which increases strongly with atomic number) and surface complexation (which apparently also increases with atomic number) the relative solution abundance patterns of the REEs produced by scavenging reactions can be quite complex.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27712919','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27712919"><span>Greening Drylands with <span class="hlt">Seawater</span> Easily and Naturally.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Moustafa, Khaled</p> <p>2017-03-01</p> <p>The sun and sea are inexhaustible sources of energy and water that could be used to transform drylands into more viable ecosystems. A sustainable and cost-effective approach is proposed for greening drylands and restoring wildlife and biodiversity in deserts using <span class="hlt">seawater</span> desert-houses (or movable <span class="hlt">seawater</span> ponds) that could offer important environmental advantages. Copyright © 2016 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29654300','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29654300"><span>Fossil black smoker yields oxygen isotopic composition of Neoproterozoic <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hodel, F; Macouin, M; Trindade, R I F; Triantafyllou, A; Ganne, J; Chavagnac, V; Berger, J; Rospabé, M; Destrigneville, C; Carlut, J; Ennih, N; Agrinier, P</p> <p>2018-04-13</p> <p>The evolution of the <span class="hlt">seawater</span> oxygen isotopic composition (δ 18 O) through geological time remains controversial. Yet, the past δ 18 O <span class="hlt">seawater</span> is key to assess past <span class="hlt">seawater</span> temperatures, providing insights into past climate change and life evolution. Here we provide a new and unprecedentedly precise δ 18 O value of -1.33 ± 0.98‰ for the Neoproterozoic bottom <span class="hlt">seawater</span> supporting a constant oxygen isotope composition through time. We demonstrate that the Aït Ahmane ultramafic unit of the ca. 760 Ma Bou Azzer ophiolite (Morocco) host a fossil black smoker-type hydrothermal system. In this system we analyzed an untapped archive for the ocean oxygen isotopic composition consisting in pure magnetite veins directly precipitated from a Neoproterozoic <span class="hlt">seawater</span>-derived fluid. Our results suggest that, while δ 18 O <span class="hlt">seawater</span> and submarine hydrothermal processes were likely similar to present day, Neoproterozoic oceans were 15-30 °C warmer on the eve of the Sturtian glaciation and the major life diversification that followed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFMPP13A2057L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFMPP13A2057L"><span>Sea <span class="hlt">ice</span> variations in the central Okhotsk Sea during the last two glacial-interglacial cycles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lo, L.; Cabedo-Sanz, P.; Lattaud, J.; Belt, S. T.; Schouten, S.; Huang, J. J.; Timmermann, A.; Zeeden, C.; Wei, K. Y.; Shen, C. C.; Hodell, D. A.; Elderfield, H.</p> <p>2016-12-01</p> <p>Sea <span class="hlt">ice</span> system as one of the critical and sensitive climate components in the Earth's climate system has experienced dramatically declination for the past few decades. Little knowledge, however, about the sea <span class="hlt">ice</span> variations in the past orbital timescales has been obtained by paleoclimatic studies due to the lack of reliable sea <span class="hlt">ice</span> proxy and age model constrain in the high productivity subpolar to polar regions. Here we present continuous 180,000 years subarctic northwestern Pacific sea <span class="hlt">ice</span> and surface temperature (SST) records in the center Okhotsk Sea, the southernmost of seasonal sea <span class="hlt">ice</span> fomration region in the Northern Hemisphere by using by using novel organic and non-destructive geochemical proxies from Site MD01-2414 (53oN, 149oE, water depth 1123 m). High resolution X-ray fluoresces scanning biogenic/terrestrial (Ba/Ti) elemental ratio represent clear glacial-interglacial cycles. Organic geochemical proxies (IP25 and TEX86) derived sea <span class="hlt">ice</span> and SST changes in the same time resolution reveal the seasonality in the center Okhotsk Sea. Sea <span class="hlt">ice</span> shows strong 23-kyr precession cycle control with modulation of 100-kyr eccentricity cycle during the peak interglacial periods (Marine Isotope Stage 5e and Holocene). On the other hand, SST represent global background climate change of 100-kyr cycle with very strong obliquity changes. According to the timeseries analyses, we argue that the sea <span class="hlt">ice</span> minimum in the center of Okhotsk Sea has mainly been controlled by the local autumn insolation. SST represent annual insolation increasing due to local summer insolation and the obliquity pacing. This study firstly demonstrated clear seasonality in the same site. Further study of the relationship between sea <span class="hlt">ice</span> and <span class="hlt">seawater</span> thermal hisotries on the orbital timescale in the subarctic Pacific is crucial in the understanding of past major climate event, e.g. Middle Pleistocene Transition and Middle Brunhes Event.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.A51F0126W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.A51F0126W"><span>Marine sources of <span class="hlt">ice</span> nucleating particles: results from phytoplankton cultures and samples collected at sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wilbourn, E.; Thornton, D.; Brooks, S. D.; Graff, J.</p> <p>2016-12-01</p> <p>The role of marine aerosols as <span class="hlt">ice</span> nucleating particles is currently poorly understood. Despite growing interest, there are remarkably few <span class="hlt">ice</span> nucleation measurements on representative marine samples. Here we present results of heterogeneous <span class="hlt">ice</span> nucleation from laboratory studies and in-situ air and sea water samples collected during NAAMES (North Atlantic Aerosol and Marine Ecosystems Study). Thalassiosira weissflogii (CCMP 1051) was grown under controlled conditions in batch cultures and the <span class="hlt">ice</span> nucleating activity depended on the growth phase of the cultures. Immersion freezing temperatures of the lab-grown diatoms were determined daily using a custom <span class="hlt">ice</span> nucleation apparatus cooled at a set rate. Our results show that the age of the culture had a significant impact on <span class="hlt">ice</span> nucleation temperature, with samples in stationary phase causing nucleation at -19.9 °C, approximately nine degrees warmer than the freezing temperature during exponential growth phase. Field samples gathered during the NAAMES II cruise in May 2016 were also tested for <span class="hlt">ice</span> nucleating ability. Two types of samples were gathered. Firstly, whole cells were fractionated by size from surface <span class="hlt">seawater</span> using a BD Biosciences Influx Cell Sorter (BD BS ISD). Secondly, aerosols were generated using the SeaSweep and subsequently size-selected using a PIXE Cascade Impactor. Samples were tested for the presence of <span class="hlt">ice</span> nucleating particles (INP) using the technique described above. There were significant differences in the freezing temperature of the different samples; of the three sample types the lab-grown cultures tested during stationary phase froze at the warmest temperatures, followed by the SeaSweep samples (-25.6 °C) and the size-fractionated cell samples (-31.3 °C). Differences in <span class="hlt">ice</span> nucleation ability may be due to size differences between the INP, differences in chemical composition of the sample, or some combination of these two factors. Results will be presented and atmospheric implications</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16141252','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16141252"><span>Exposure to oil mist and oil <span class="hlt">vapour</span> during offshore drilling in norway, 1979-2004.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Steinsvåg, Kjersti; Bråtveit, Magne; Moen, Bente E</p> <p>2006-03-01</p> <p>To describe personal exposure to airborne hydrocarbon contaminants (oil mist and oil <span class="hlt">vapour</span>) from 1979 to 2004 in the mud-handling areas of offshore drilling facilities operating on the Norwegian continental shelf when drilling with oil-based muds. Qualitative and quantitative information was gathered during visits to companies involved in offshore oil and gas production in Norway. Monitoring reports on oil mist and oil <span class="hlt">vapour</span> exposure covered 37 drilling facilities. Exposure data were analysed using descriptive statistics and by constructing linear mixed-effects models. Samples had been taken during the use of three generations of hydrocarbon base oils, namely diesel oils (1979-1984), low-aromatic mineral oils (1985-1997) and non-aromatic mineral oils (1998-2004). Sampling done before 1984 showed high exposure to diesel <span class="hlt">vapour</span> (arithmetic mean, AM = 1217 mg m(-3)). When low-aromatic mineral oils were used, the exposure to oil mist and oil <span class="hlt">vapour</span> was 4.3 and 36 mg m(-3), and the respective AMs for non-aromatic mineral oils were reduced to 0.54 and 16 mg m(-3). Downward time trends were indicated for both oil mist (6% per year) and oil <span class="hlt">vapour</span> (8% per year) when the year of monitoring was introduced as a fixed effect in a linear mixed-effects model analysis. Rig type, technical control measures and mud temperature significantly determined exposure to oil mist. Rig type, type of base oil, viscosity of the base oil, work area, mud temperature and season significantly determined exposure to oil <span class="hlt">vapour</span>. Major decreases in variability were found for the between-rig components. Exposure to oil mist and oil <span class="hlt">vapour</span> declined over time in the mud-handling areas of offshore drilling facilities. Exposure levels were associated with rig type, mud temperature, technical control measures, base oil, viscosity of the base oil, work area and season.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11413931','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11413931"><span>In-vitro and in-vivo anti-Trichophyton activity of essential oils by <span class="hlt">vapour</span> contact.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Inouye, S; Uchida, K; Yamaguchi, H</p> <p>2001-05-01</p> <p>The minimum inhibitory doses (MIDs) of essential oils by <span class="hlt">vapour</span> contact to inhibit the growth of Trichophyton mentagrophytes and Trichophyton rubrum on agar medium were determined using airtight boxes. Among seven essential oils examined, cinnamon bark oil showed the least MID, followed by lemongrass, thyme and perilla oils. Lavender and tea tree oils showed moderate MID, and citron oil showed the highest MID, being 320 times higher than that of cinnamon bark oil. The MID values were less than the minimum inhibitory concentration (MIC) values determined by agar dilution assay. Furthermore, the minimum agar concentration (MAC) of essential oils absorbed from <span class="hlt">vapour</span> was determined at the time of MID determination as the second antifungal measure. The MAC value by <span class="hlt">vapour</span> contact was 1.4 to 4.7 times less than the MAC remaining in the agar at the time of MIC determination by agar dilution assay. Using selected essential oils, the anti-Trichophyton activity by <span class="hlt">vapour</span> contact was examined in more detail. Lemongrass, thyme and perilla oils killed the conidia, inhibited germination and hyphal elongation at 1-4 micrograms ml-1 air, whereas lavender oil was effective at 40-160 micrograms ml-1 air. The in-vivo efficacy of thyme and perilla oils by <span class="hlt">vapour</span> contact was shown against an experimental tinea pedis in guinea pigs infected with T. mentagrophytes. These results indicated potent anti-Trichophyton action of essential oils by <span class="hlt">vapour</span> contact.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/10984211','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/10984211"><span>The effect of perfluorocarbon <span class="hlt">vapour</span> on the measurement of respiratory tidal volume during partial liquid ventilation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Davies, M W; Dunster, K R</p> <p>2000-08-01</p> <p>During partial liquid ventilation perfluorocarbon <span class="hlt">vapour</span> is present in the exhaled gases. The volumes of these gases are measured by pneumotachometers. Error in measuring tidal volumes will give erroneous measurement of lung compliance during partial liquid ventilation. We aim to compare measured tidal volumes with and without perfluorocarbon <span class="hlt">vapour</span> using tidal volumes suitable for use in neonates. Tidal volumes were produced with a 100 ml calibration syringe from 20 to 100 ml and with a calibrated Harvard rodent ventilator from 2.5 to 20 ml. Control tidal volumes were drawn from a humidifier chamber containing water <span class="hlt">vapour</span> and the PFC tidal volumes were drawn from a humidifier chamber containing water and perfluorocarbon (FC-77) <span class="hlt">vapour</span>. Tidal volumes were measured by a fixed orifice, target, differential pressure flowmeter (VenTrak) or a hot-wire anenometer (Bear Cub) placed between the calibration syringe or ventilator and the humidifier chamber. All tidal volumes measured with perfluorocarbon <span class="hlt">vapour</span> were increased compared with control (ANOVA p < 0.001 and post t-test p < 0.0001). Measured tidal volume increased from 7 to 16% with the fixed orifice type flow-meter, and from 35 to 41% with the hot-wire type. In conclusion, perfluorocarbon <span class="hlt">vapour</span> flowing through pneumotachometers gives falsely high tidal volume measurements. Calculation of lung compliance must take into account the effect of perfluorocarbon <span class="hlt">vapour</span> on the measurement of tidal volume.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005AtmRe..74..253C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005AtmRe..74..253C"><span>GPS water <span class="hlt">vapour</span> tomography: preliminary results from the ESCOMPTE field experiment</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Champollion, C.; Masson, F.; Bouin, M.-N.; Walpersdorf, A.; Doerflinger, E.; Bock, O.; Van Baelen, J.</p> <p>2005-03-01</p> <p>Water <span class="hlt">vapour</span> plays a major role in atmospheric processes but remains difficult to quantify due to its high variability in time and space and the sparse set of available measurements. The GPS has proved its capacity to measure the integrated water <span class="hlt">vapour</span> at zenith with the same accuracy as other methods. Recent studies show that it is possible to quantify the integrated water <span class="hlt">vapour</span> in the line of sight of the GPS satellite. These observations can be used to study the 3D heterogeneity of the troposphere using tomographic techniques. We develop three-dimensional tomographic software to model the three-dimensional distribution of the tropospheric water <span class="hlt">vapour</span> from GPS data. First, the tomographic software is validated by simulations based on the realistic ESCOMPTE GPS network configuration. Without a priori information, the absolute value of water <span class="hlt">vapour</span> is less resolved as opposed to relative horizontal variations. During the ESCOMPTE field experiment, a dense network of 17 dual frequency GPS receivers was operated for 2 weeks within a 20×20-km area around Marseille (southern France). The network extends from sea level to the top of the Etoile chain (˜700 m high). Optimal results have been obtained with time windows of 30-min intervals and input data evaluation every 15 min. The optimal grid for the ESCOMTE geometrical configuration has a horizontal step size of 0.05°×0.05° and 500 m vertical step size. Second, we have compared the results of real data inversions with independent observations. Three inversions have been compared to three successive radiosonde launches and shown to be consistent. A good resolution compared to the a priori information is obtained up to heights of 3000 m. A humidity spike at 4000-m altitude remains unresolved. The reason is probably that the signal is spread homogeneously over the whole network and that such a feature is not resolvable by tomographic techniques. The results of our pure GPS inversion show a correlation with</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.P53D2661H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.P53D2661H"><span>Compatibility of amino acids in <span class="hlt">ice</span> Ih and high-pressure phases: implications for the origin of life</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hao, J.; Giovenco, E.; Pedreira-Segade, U.; Montagnac, G.; Daniel, I.</p> <p>2017-12-01</p> <p>Icy environments may have been common on the early Earth due to the faint young sun. Previous studies have proposed that the formation of large icy bodies in the early ocean could concentrate the building blocks of life in eutectic fluids and therefore facilitate the polymerization of monomers. This hypothesis is based on the untested assumption that organic molecules are virtually incompatible in <span class="hlt">ice</span> Ih. In this study, we conducted freezing experiments to explore the partitioning behavior of selected amino acids (glycine, L-alanine, L-proline, and L-phenylalanine) between <span class="hlt">ice</span> Ih and aqueous solutions analogous to <span class="hlt">seawater</span>. We let <span class="hlt">ice</span> crystals grow slowly from a few seeds in equilibrium with the solution and used Raman spectroscopy to analyze in situ the relative concentrations of amino acids in the <span class="hlt">ice</span> and aqueous solution. During freezing, there was no precipitation of amino acid crystals, indicating that the concentrations in solution never reached their solubility limit, even when the droplet was mostly frozen. Analyses of the Raman spectra of <span class="hlt">ice</span> and eutectic solution showed that considerable amounts of amino acids existed in the <span class="hlt">ice</span> phase with partition coefficients ranging between 0.2 and 0.5. This study also explored the partitioning of amino acids between other phases of <span class="hlt">ice</span> (<span class="hlt">ice</span> VI and <span class="hlt">ice</span> VII) and solutions at high pressures and observed similar results. These observations implied little incompatibility of amino acids in <span class="hlt">ice</span> during the freezing of the solutions, rendering the hypothesis of a cold origin of life unwarranted. However, incorporation into <span class="hlt">ice</span> could significantly improve the efficiency of extraterrestrial transport of small organics. Therefore, this study supports the hypothesis of extraterrestrial delivery of organic molecules in the icy comets and asteroids to the primitive Earth as suggested by an increasing number of independent observations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1996MeScT...7..742L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1996MeScT...7..742L"><span>Dew-point measurements at high water <span class="hlt">vapour</span> pressure</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lomperski, S.; Dreier, J.</p> <p>1996-05-01</p> <p>A dew-point meter capable of measuring humidity at high <span class="hlt">vapour</span> pressure and high temperature has been constructed and tested. Humidity measurements in pure steam were made over the temperature range 100 - 1500957-0233/7/5/003/img1C and a <span class="hlt">vapour</span> pressure range of 1 - 4 bar. The dew-point meter performance was assessed by comparing measurements with a pressure transmitter and agreement between the two was within 0957-0233/7/5/003/img2% relative humidity. Humidity measurements in steam - air mixtures were also made and the dew-point meter readings were compared to those of a zirconia oxygen sensor. For these tests the dew-point meter readings were generally within 0957-0233/7/5/003/img2% relative humidity of the oxygen sensor measurements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1252140-macroporous-monoliths-trace-metal-extraction-from-seawater','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1252140-macroporous-monoliths-trace-metal-extraction-from-seawater"><span>Macroporous monoliths for trace metal extraction from <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Yue, Yanfeng; Mayes, Richard T.; Gill, Gary; ...</p> <p>2015-05-29</p> <p>The viability of <span class="hlt">seawater</span>-based uranium recovery depends on the uranium adsorption rate and capacity, since the concentration of uranium in the oceans is relatively low (3.3 gL -1). An important consideration for a fast adsorption is to maximize the adsorption properties of adsorbents such as surface areas and pore structures, which can greatly improve the kinetics of uranium extraction and the adsorption capacity simultaneously. Following this consideration, macroporous monolith adsorbents were prepared from the copolymerization of acrylonitrile (AN) and N,N -methylenebis(acrylamide) (MBAAm) based on a cryogel method using both hydrophobic and hydrophilic monomers. The monolithic sorbents were tested with simulatedmore » <span class="hlt">seawater</span> containing a high uranyl concentration (–6 ppm) and the uranium adsorption results showed that the adsorption capacities are strongly influenced by the ratio of monomer to the crosslinker, i.e., the density of the amidoxime groups. Furthermore, the preliminary <span class="hlt">seawater</span> testing indicates the high salinity content of <span class="hlt">seawater</span> does not hinder the adsorption of uranium.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21926068','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21926068"><span>Oil mist and <span class="hlt">vapour</span> concentrations from drilling fluids: inter- and intra-laboratory comparison of chemical analyses.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Galea, Karen S; Searl, Alison; Sánchez-Jiménez, Araceli; Woldbæk, Torill; Halgard, Kristin; Thorud, Syvert; Steinsvåg, Kjersti; Krüger, Kirsti; Maccalman, Laura; Cherrie, John W; van Tongeren, Martie</p> <p>2012-01-01</p> <p>There are no recognized analytical methods for measuring oil mist and <span class="hlt">vapours</span> arising from drilling fluids used in offshore petroleum drilling industry. To inform the future development of improved methods of analysis for oil mist and <span class="hlt">vapours</span> this study assessed the inter- and intra-laboratory variability in oil mist and <span class="hlt">vapour</span> analysis. In addition, sample losses during transportation and storage were assessed. Replicate samples for oil mist and <span class="hlt">vapour</span> were collected using the 37-mm Millipore closed cassette and charcoal tube assembly. Sampling was conducted in a simulated shale shaker room, similar to that found offshore for processing drilling fluids. Samples were analysed at two different laboratories, one in Norway and one in the UK. Oil mist samples were analysed using Fourier transform infrared spectroscopy (FTIR), while oil <span class="hlt">vapour</span> samples were analysed by gas chromatography (GC). The comparison of replicate samples showed substantial within- and between-laboratory variability in reported oil mist concentrations. The variability in oil <span class="hlt">vapour</span> results was considerably reduced compared to oil mist, provided that a common method of calibration and quantification was adopted. The study also showed that losses can occur during transportation and storage of samples. There is a need to develop a harmonized method for the quantification of oil mist on filter and oil <span class="hlt">vapour</span> on charcoal supported by a suitable proficiency testing scheme for laboratories involved in the analysis of occupational hygiene samples for the petroleum industry. The uncertainties in oil mist and <span class="hlt">vapour</span> measurement have substantial implications in relation to compliance with occupational exposure limits and also in the reliability of any exposure-response information reported in epidemiological studies.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_11");'>11</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li class="active"><span>13</span></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_13 --> <div id="page_14" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="261"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26339489','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26339489"><span><span class="hlt">Ice</span> swimming - '<span class="hlt">Ice</span> Mile' and '1 km <span class="hlt">Ice</span> event'.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Knechtle, Beat; Rosemann, Thomas; Rüst, Christoph A</p> <p>2015-01-01</p> <p><span class="hlt">Ice</span> swimming for 1 mile and 1 km is a new discipline in open-water swimming since 2009. This study examined female and male performances in swimming 1 mile ('<span class="hlt">Ice</span> Mile') and 1 km ('1 km <span class="hlt">Ice</span> event') in water of 5 °C or colder between 2009 and 2015 with the hypothesis that women would be faster than men. Between 2009 and 2015, 113 men and 38 women completed one '<span class="hlt">Ice</span> Mile' and 26 men and 13 completed one '1 km <span class="hlt">Ice</span> event' in water colder than +5 °C following the rules of International <span class="hlt">Ice</span> Swimming Association (IISA). Differences in performance between women and men were determined. Sex difference (%) was calculated using the equation ([time for women] - [time for men]/[time for men] × 100). For '<span class="hlt">Ice</span> Mile', a mixed-effects regression model with interaction analyses was used to investigate the influence of sex and environmental conditions on swimming speed. The association between water temperature and swimming speed was assessed using Pearson correlation analyses. For '<span class="hlt">Ice</span> Mile' and '1 km <span class="hlt">Ice</span> event', the best men were faster than the best women. In '<span class="hlt">Ice</span> Mile', calendar year, number of attempts, water temperature and wind chill showed no association with swimming speed for both women and men. For both women and men, water temperature was not correlated to swimming speed in both '<span class="hlt">Ice</span> Mile' and '1 km <span class="hlt">Ice</span> event'. In water colder than 5 °C, men were faster than women in '<span class="hlt">Ice</span> Mile' and '1 km <span class="hlt">Ice</span> event'. Water temperature showed no correlation to swimming speed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-200910220008HQ.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-200910220008HQ.html"><span><span class="hlt">Ice</span> Bridge Antarctic Sea <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2009-10-21</p> <p>Sea <span class="hlt">ice</span> is seen out the window of NASA's DC-8 research aircraft as it flies 2,000 feet above the Bellingshausen Sea in West Antarctica on Wednesday, Oct., 21, 2009. This was the fourth science flight of NASA’s Operation <span class="hlt">Ice</span> Bridge airborne Earth science mission to study Antarctic <span class="hlt">ice</span> sheets, sea <span class="hlt">ice</span>, and <span class="hlt">ice</span> shelves. Photo Credit: (NASA/Jane Peterson)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21858276','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21858276"><span>The <span class="hlt">vapour</span> of imidazolium-based ionic liquids: a mass spectrometry study.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Deyko, A; Lovelock, K R J; Licence, P; Jones, R G</p> <p>2011-10-06</p> <p>Eight common dialkylimidazolium-based ionic liquids have been successfully evaporated in ultra-high vacuum and their <span class="hlt">vapours</span> analysed by line of sight mass spectrometry using electron ionisation. The ionic liquids investigated were 1-alkyl-3-methylimidazolium bis[(trifluoromethane)sulfonyl]imide, [C(n)C(1)Im][Tf(2)N] (where n = 2, 4, 6, 8), 1-alkyl-3-methylimidazolium tetrafluoroborate, [C(n)C(1)Im][BF(4)] (where n = 4, 8), 1-butyl-3-methylimidazolium octylsulfate, [C(4)C(1)Im][C(8)OSO(3)] and 1-butyl-3-methylimidazolium tetrachloroferrate, [C(4)C(1)Im][FeCl(4)]. All ionic liquids studied here evaporated as neutral ion pairs; no evidence of decomposition products in the <span class="hlt">vapour</span> phase were observed. Key fragment cations of the ionised <span class="hlt">vapour</span> of the ionic liquids are identified. The appearance energies, E(app), of the parent cation were measured and used to estimate the ionisation energies, E(i), for the <span class="hlt">vapour</span> phase neutral ion pairs. Measured ionisation energies ranged from 10.5 eV to 13.0 eV. Using both the identity and E(app) values, the fragmentation pathways for a number of fragment cations are postulated. It will be shown that the enthalpy of vaporisation, Δ(vap)H, can successfully be measured using more than one fragment cation, although caution is required as many fragment cations can also be formed by ionisation of decomposition products.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AIPC.1805g0002N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AIPC.1805g0002N"><span>Calcium extraction from brine water and <span class="hlt">seawater</span> using oxalic acid</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Natasha, Nadia Chrisayu; Lalasari, Latifa Hanum</p> <p>2017-01-01</p> <p>Calcium can be extracted not only from rocks but also from natural liquor such as <span class="hlt">seawater</span> and brine water. In order to extract the calcium from <span class="hlt">seawater</span> and brine water, oxalic acid was used in this research. Effect of variations of the volume of the oxalic acid at a constant concentration in <span class="hlt">seawater</span> and brine water to produce calcium was investigated. The concentration of oxalic acid was 100 g/l and the variations of its volume were 2 ml, 4 ml, 6 ml, 8 ml, 10 ml, 20 ml, 30 ml, 40 ml, and 50 ml. The used <span class="hlt">seawater</span> and brine water were firstly evaporated from 100 ml into 50 ml and then the oxalic acid was added into them with mixing to produce the calcium precipitates. The precipitates were analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM) and the filtrates were analyzed by inductively coupled plasma-optical emission spectrometry (ICP-OES). The SEM analysis showed that the precipitates from brine water were consisted of only calcium compound while from <span class="hlt">seawater</span> sodium one was also found along with calcium compound. The XRD analysis showed that the calcium was present in the form of calcium oxalate for both <span class="hlt">seawater</span> and brine water. The ICP-OES analysis of the filtrate from <span class="hlt">seawater</span> precipitation showed that the its calcium content was decreased from 826.20 ppm to 0.04 ppm while from brine water, it decreased from 170.06 ppm to 1.96 ppm. These results showed that both <span class="hlt">seawater</span> and brine water have the potential to be a raw material for calcium production.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26141510','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26141510"><span>Different physiological and behavioural effects of e-cigarette <span class="hlt">vapour</span> and cigarette smoke in mice.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ponzoni, L; Moretti, M; Sala, M; Fasoli, F; Mucchietto, V; Lucini, V; Cannazza, G; Gallesi, G; Castellana, C N; Clementi, F; Zoli, M; Gotti, C; Braida, D</p> <p>2015-10-01</p> <p>Nicotine is the primary addictive substance in tobacco smoke and electronic cigarette (e-cig) <span class="hlt">vapour</span>. Methodological limitations have made it difficult to compare the role of the nicotine and non-nicotine constituents of tobacco smoke. The aim of this study was to compare the effects of traditional cigarette smoke and e-cig <span class="hlt">vapour</span> containing the same amount of nicotine in male BALB/c mice exposed to the smoke of 21 cigarettes or e-cig <span class="hlt">vapour</span> containing 16.8 mg of nicotine delivered by means of a mechanical ventilator for three 30-min sessions/day for seven weeks. One hour after the last session, half of the animals were sacrificed for neurochemical analysis, and the others underwent mecamylamine-precipitated or spontaneous withdrawal for the purposes of behavioural analysis. Chronic intermittent non-contingent, second-hand exposure to cigarette smoke or e-cig <span class="hlt">vapour</span> led to similar brain cotinine and nicotine levels, similar urine cotinine levels and the similar up-regulation of α4β2 nicotinic acetylcholine receptors in different brain areas, but had different effects on body weight, food intake, and the signs of mecamylamine-precipitated and spontaneous withdrawal episodic memory and emotional responses. The findings of this study demonstrate for the first time that e-cig <span class="hlt">vapour</span> induces addiction-related neurochemical, physiological and behavioural alterations. The fact that inhaled cigarette smoke and e-cig <span class="hlt">vapour</span> have partially different dependence-related effects indicates that compounds other than nicotine contribute to tobacco dependence. Copyright © 2015 Elsevier B.V. and ECNP. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27403638','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27403638"><span>Atomic-scale Studies of Uranium Oxidation and Corrosion by Water <span class="hlt">Vapour</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Martin, T L; Coe, C; Bagot, P A J; Morrall, P; Smith, G D W; Scott, T; Moody, M P</p> <p>2016-07-12</p> <p>Understanding the corrosion of uranium is important for its safe, long-term storage. Uranium metal corrodes rapidly in air, but the exact mechanism remains subject to debate. Atom Probe Tomography was used to investigate the surface microstructure of metallic depleted uranium specimens following polishing and exposure to moist air. A complex, corrugated metal-oxide interface was observed, with approximately 60 at.% oxygen content within the oxide. Interestingly, a very thin (~5 nm) interfacial layer of uranium hydride was observed at the oxide-metal interface. Exposure to deuterated water <span class="hlt">vapour</span> produced an equivalent deuteride signal at the metal-oxide interface, confirming the hydride as originating via the water <span class="hlt">vapour</span> oxidation mechanism. Hydroxide ions were detected uniformly throughout the oxide, yet showed reduced prominence at the metal interface. These results support a proposed mechanism for the oxidation of uranium in water <span class="hlt">vapour</span> environments where the transport of hydroxyl species and the formation of hydride are key to understanding the observed behaviour.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016NatSR...625618M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016NatSR...625618M"><span>Atomic-scale Studies of Uranium Oxidation and Corrosion by Water <span class="hlt">Vapour</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Martin, T. L.; Coe, C.; Bagot, P. A. J.; Morrall, P.; Smith, G. D. W.; Scott, T.; Moody, M. P.</p> <p>2016-07-01</p> <p>Understanding the corrosion of uranium is important for its safe, long-term storage. Uranium metal corrodes rapidly in air, but the exact mechanism remains subject to debate. Atom Probe Tomography was used to investigate the surface microstructure of metallic depleted uranium specimens following polishing and exposure to moist air. A complex, corrugated metal-oxide interface was observed, with approximately 60 at.% oxygen content within the oxide. Interestingly, a very thin (~5 nm) interfacial layer of uranium hydride was observed at the oxide-metal interface. Exposure to deuterated water <span class="hlt">vapour</span> produced an equivalent deuteride signal at the metal-oxide interface, confirming the hydride as originating via the water <span class="hlt">vapour</span> oxidation mechanism. Hydroxide ions were detected uniformly throughout the oxide, yet showed reduced prominence at the metal interface. These results support a proposed mechanism for the oxidation of uranium in water <span class="hlt">vapour</span> environments where the transport of hydroxyl species and the formation of hydride are key to understanding the observed behaviour.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007DPS....39.2424L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007DPS....39.2424L"><span>Preliminary Martian Atmospheric Water <span class="hlt">Vapour</span> Column Abundances with Mars Climate Sounder</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lolachi, Ramin; Irwin, P. G. J.; Teanby, N.; Calcutt, S.; Howett, C. J. A.; Bowles, N. E.; Taylor, F. W.; Schofield, J. T.; Kleinboehl, A.; McCleese, D. J.</p> <p>2007-12-01</p> <p>Mars Climate Sounder (MCS) is an infra-red radiometer on board NASA's Mars Reconnaissance Orbiter (MRO) launched in August 2005 and now orbiting Mars in a near circular polar orbit. MCS has nine spectral channels in the range 0.3-50 µm. Goals of MCS include global characterization of atmospheric temperature, dust and water profiles observing temporal and spatial variation. Using Oxford University's multivariate retrieval algorithm, NEMESIS, we present preliminary determinations of the water <span class="hlt">vapour</span> column abundance in the Martian atmosphere during the period September-October 2006 (Ls range 111-129°, i.e. northern hemisphere summer). A combination of spectral channels inside and outside the water <span class="hlt">vapour</span> rotation band (at 50 µm) are used to retrieve the column abundances mainly using nadir observations (as aerosol opacity is less important relative to water <span class="hlt">vapour</span> opacity in nadir viewing geometry). We then compare these column abundances to earlier results from the Viking Orbiter Mars Atmospheric Water Detectors (MAWD) and the Thermal Emission Spectrometer (TES) on Mars Global Surveyor.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4941397','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4941397"><span>Atomic-scale Studies of Uranium Oxidation and Corrosion by Water <span class="hlt">Vapour</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Martin, T. L.; Coe, C.; Bagot, P. A. J.; Morrall, P.; Smith, G. D. W; Scott, T.; Moody, M. P.</p> <p>2016-01-01</p> <p>Understanding the corrosion of uranium is important for its safe, long-term storage. Uranium metal corrodes rapidly in air, but the exact mechanism remains subject to debate. Atom Probe Tomography was used to investigate the surface microstructure of metallic depleted uranium specimens following polishing and exposure to moist air. A complex, corrugated metal-oxide interface was observed, with approximately 60 at.% oxygen content within the oxide. Interestingly, a very thin (~5 nm) interfacial layer of uranium hydride was observed at the oxide-metal interface. Exposure to deuterated water <span class="hlt">vapour</span> produced an equivalent deuteride signal at the metal-oxide interface, confirming the hydride as originating via the water <span class="hlt">vapour</span> oxidation mechanism. Hydroxide ions were detected uniformly throughout the oxide, yet showed reduced prominence at the metal interface. These results support a proposed mechanism for the oxidation of uranium in water <span class="hlt">vapour</span> environments where the transport of hydroxyl species and the formation of hydride are key to understanding the observed behaviour. PMID:27403638</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009P%26SS...57.1043C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009P%26SS...57.1043C"><span>MEDUSA: The ExoMars experiment for in-situ monitoring of dust and water <span class="hlt">vapour</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Colangeli, L.; Lopez-Moreno, J. J.; Nørnberg, P.; Della Corte, V.; Esposito, F.; Mazzotta Epifani, E.; Merrison, J.; Molfese, C.; Palumbo, P.; Rodriguez-Gomez, J. F.; Rotundi, A.; Visconti, G.; Zarnecki, J. C.; The International Medusa Team</p> <p>2009-07-01</p> <p>Dust and water <span class="hlt">vapour</span> are fundamental components of the Martian atmosphere. In view of tracing the past environmental conditions on Mars, that possibly favoured the appearing of life forms, it is important to study the present climate and its evolution. Here dust and water <span class="hlt">vapour</span> have (and have had) strong influence. Of major scientific interest is the quantity and physical, chemical and electrical properties of dust and the abundance of water <span class="hlt">vapour</span> dispersed in the atmosphere and their exchange with the surface. Moreover, in view of the exploration of the planet with automated systems and in the future by manned missions, it is of primary importance to analyse the hazards linked to these environmental factors. The Martian Environmental Dust Systematic Analyser (MEDUSA) experiment, included in the scientific payload of the ESA ExoMars mission, accommodates a complement of sensors, based on optical detection and cumulative mass deposition, that aims to study dust and water <span class="hlt">vapour</span> in the lower Martian atmosphere. The goals are to study, for the first time, in-situ and quantitatively, physical properties of the airborne dust, including the cumulative dust mass flux, the dust deposition rate, the physical and electrification properties, the size distribution of sampled particles and the atmospheric water <span class="hlt">vapour</span> abundance versus time.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27351725','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27351725"><span><span class="hlt">Vapours</span> of US and EU Market Leader Electronic Cigarette Brands and Liquids Are Cytotoxic for Human Vascular Endothelial Cells.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Putzhammer, Raphaela; Doppler, Christian; Jakschitz, Thomas; Heinz, Katharina; Förste, Juliane; Danzl, Katarina; Messner, Barbara; Bernhard, David</p> <p>2016-01-01</p> <p>The present study was conducted to provide toxicological data on e-cigarette <span class="hlt">vapours</span> of different e-cigarette brands and liquids from systems viewed as leaders in the e-cigarette market and to compare e-cigarette <span class="hlt">vapour</span> toxicity to the toxicity of conventional strong high-nicotine cigarette smoke. Using an adapted version of a previously constructed cigarette smoke constituent sampling device, we collected the hydrophilic fraction of e-cigarette <span class="hlt">vapour</span> and exposed human umbilical vein endothelial cells (HUVECs) to the mixture of compounds present in the <span class="hlt">vapour</span> of 4 different single-use e-cigarettes, 6 different liquid <span class="hlt">vapours</span> produced by the same refillable e-cigarette, and one e-cigarette with an exchangeable liquid cartridge. After incubation of cells with various concentrations and for various periods of time we analysed cell death induction, proliferation rates, the occurrence of intra-cellular reactive oxygen species, cell morphology, and we also measured e-cigarette heating coil temperatures. Overall, conventional cigarette smoke extract showed the most severe impact on endothelial cells. However, some e-cigarette <span class="hlt">vapour</span> extracts showed high cytotoxicity, inhibition of cell proliferation, and alterations in cell morphology, which were comparable to conventional high-nicotine cigarettes. The <span class="hlt">vapours</span> generated from different liquids using the same e-cigarette show substantial differences, pointing to the liquids as an important source for toxicity. E-cigarette <span class="hlt">vapour</span>-mediated induction of oxidative stress was significant in one out of the 11 analysed <span class="hlt">vapours</span>. There is a high variability in the acute cytotoxicity of e-cigarette <span class="hlt">vapours</span> depending on the liquid and on the e-cigarettes used. Some products showed toxic effects close to a conventional high-nicotine cigarette. Liquid nicotine, menthol content, and the formation of acute intracellular reactive oxygen species do not seem to be the central elements in e-cigarette <span class="hlt">vapour</span> toxicity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4924852','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4924852"><span><span class="hlt">Vapours</span> of US and EU Market Leader Electronic Cigarette Brands and Liquids Are Cytotoxic for Human Vascular Endothelial Cells</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Putzhammer, Raphaela; Doppler, Christian; Jakschitz, Thomas; Heinz, Katharina; Förste, Juliane; Danzl, Katarina; Messner, Barbara; Bernhard, David</p> <p>2016-01-01</p> <p>The present study was conducted to provide toxicological data on e-cigarette <span class="hlt">vapours</span> of different e-cigarette brands and liquids from systems viewed as leaders in the e-cigarette market and to compare e-cigarette <span class="hlt">vapour</span> toxicity to the toxicity of conventional strong high-nicotine cigarette smoke. Using an adapted version of a previously constructed cigarette smoke constituent sampling device, we collected the hydrophilic fraction of e-cigarette <span class="hlt">vapour</span> and exposed human umbilical vein endothelial cells (HUVECs) to the mixture of compounds present in the <span class="hlt">vapour</span> of 4 different single-use e-cigarettes, 6 different liquid <span class="hlt">vapours</span> produced by the same refillable e-cigarette, and one e-cigarette with an exchangeable liquid cartridge. After incubation of cells with various concentrations and for various periods of time we analysed cell death induction, proliferation rates, the occurrence of intra-cellular reactive oxygen species, cell morphology, and we also measured e-cigarette heating coil temperatures. Overall, conventional cigarette smoke extract showed the most severe impact on endothelial cells. However, some e-cigarette <span class="hlt">vapour</span> extracts showed high cytotoxicity, inhibition of cell proliferation, and alterations in cell morphology, which were comparable to conventional high-nicotine cigarettes. The <span class="hlt">vapours</span> generated from different liquids using the same e-cigarette show substantial differences, pointing to the liquids as an important source for toxicity. E-cigarette <span class="hlt">vapour</span>-mediated induction of oxidative stress was significant in one out of the 11 analysed <span class="hlt">vapours</span>. There is a high variability in the acute cytotoxicity of e-cigarette <span class="hlt">vapours</span> depending on the liquid and on the e-cigarettes used. Some products showed toxic effects close to a conventional high-nicotine cigarette. Liquid nicotine, menthol content, and the formation of acute intracellular reactive oxygen species do not seem to be the central elements in e-cigarette <span class="hlt">vapour</span> toxicity. PMID:27351725</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21535722','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21535722"><span>Rested and stressed farmed Atlantic cod (Gadus morhua) chilled in <span class="hlt">ice</span> or slurry and effects on quality.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Digre, Hanne; Erikson, Ulf; Aursand, Ida G; Gallart-Jornet, Lorena; Misimi, Ekrem; Rustad, Turid</p> <p>2011-01-01</p> <p>The main objectives of this study were to investigate (1) whether rested harvest of farmed cod was better maintained by chilling with slurry rather than by traditional <span class="hlt">ice</span> storage, (2) whether chilling with slurry would be a feasible chilling method to assure low core temperatures (≤0 °C) at packing of gutted fish, and (3) the effects of superchilling compared with traditional <span class="hlt">ice</span> on selected quality parameters of cod during storage. In the experiment, <span class="hlt">seawater</span> slurry at -2.0 ± 0.3 °C was used. Anesthetized (AQUI-S™), percussion stunned, and stressed cod chilled in slurry were compared. Cod stored on <span class="hlt">ice</span> were used as reference group. The fish were evaluated at the day of slaughter, and after 7 and 14 d of storage according to handling stress (initial muscle pH, muscle twitches, rigor mortis), core temperatures, quality index method, microbial counts, weight changes, salt and water content, water distribution, pH, adenosine triphosphate-degradation products, K-value, water-holding capacity, fillet color, and texture. Chilling cod in slurry was more rapid than chilling in <span class="hlt">ice</span>. Prechilling (1 d) of cod in slurry before subsequent <span class="hlt">ice</span> storage resulted in lower quality 7 d postmortem compared with both <span class="hlt">ice</span> and continuous slurry storage. The potential advantages of superchilling became more prominent after 14 d with lower microbiological activity, better maintenance of freshness (lower total quality index scores and lower K-values) compared with fish stored on <span class="hlt">ice</span>. A drawback with slurry-stored fish was that cloudy eyes developed earlier, in addition to weight gain and salt uptake compared to <span class="hlt">ice</span>-stored fish. Practical Application: Chilling is an essential operation in any fish-processing plant. This manuscript addresses different applications of slurry <span class="hlt">ice</span> in the processing and storage of Atlantic cod. Cod quality was assessed after 7 and 14 d of <span class="hlt">iced</span> and superchilled storage.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20170011211','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20170011211"><span><span class="hlt">Ice</span> Crystal <span class="hlt">Icing</span> Research at NASA</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Flegel, Ashlie B.</p> <p>2017-01-01</p> <p><span class="hlt">Ice</span> crystals found at high altitude near convective clouds are known to cause jet engine power-loss events. These events occur due to <span class="hlt">ice</span> crystals entering a propulsion system's core flowpath and accreting <span class="hlt">ice</span> resulting in events such as uncommanded loss of thrust (rollback), engine stall, surge, and damage due to <span class="hlt">ice</span> shedding. As part of a community with a growing need to understand the underlying physics of <span class="hlt">ice</span> crystal <span class="hlt">icing</span>, NASA has been performing experimental efforts aimed at providing datasets that can be used to generate models to predict the <span class="hlt">ice</span> accretion inside current and future engine designs. Fundamental <span class="hlt">icing</span> physics studies on particle impacts, accretion on a single airfoil, and <span class="hlt">ice</span> accretions observed during a rollback event inside a full-scale engine in the Propulsion Systems Laboratory are summarized. Low fidelity code development using the results from the engine tests which identify key parameters for <span class="hlt">ice</span> accretion risk and the development of high fidelity codes are described. These activities have been conducted internal to NASA and through collaboration efforts with industry, academia, and other government agencies. The details of the research activities and progress made to date in addressing <span class="hlt">ice</span> crystal <span class="hlt">icing</span> research challenges are discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20170006539','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20170006539"><span><span class="hlt">Ice</span> Crystal <span class="hlt">Icing</span> Research at NASA</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Flegel, Ashlie B.</p> <p>2017-01-01</p> <p><span class="hlt">Ice</span> crystals found at high altitude near convective clouds are known to cause jet engine power-loss events. These events occur due to <span class="hlt">ice</span> crystals entering a propulsion systems core flowpath and accreting <span class="hlt">ice</span> resulting in events such as uncommanded loss of thrust (rollback), engine stall, surge, and damage due to <span class="hlt">ice</span> shedding. As part of a community with a growing need to understand the underlying physics of <span class="hlt">ice</span> crystal <span class="hlt">icing</span>, NASA has been performing experimental efforts aimed at providing datasets that can be used to generate models to predict the <span class="hlt">ice</span> accretion inside current and future engine designs. Fundamental <span class="hlt">icing</span> physics studies on particle impacts, accretion on a single airfoil, and <span class="hlt">ice</span> accretions observed during a rollback event inside a full-scale engine in the Propulsion Systems Laboratory are summarized. Low fidelity code development using the results from the engine tests which identify key parameters for <span class="hlt">ice</span> accretion risk and the development of high fidelity codes are described. These activities have been conducted internal to NASA and through collaboration efforts with industry, academia, and other government agencies. The details of the research activities and progress made to date in addressing <span class="hlt">ice</span> crystal <span class="hlt">icing</span> research challenges are discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AGUFM.B23B0196O','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AGUFM.B23B0196O"><span>Abiotic Nitrous Oxide Production in Natural and Artificial <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ochoa, H.; Stanton, C. L.; Cavazos, A. R.; Ostrom, N. E.; Glass, J. B.</p> <p>2014-12-01</p> <p>The ocean contributes approximately one third of global sources of nitrous oxide (N2O) to the atmosphere. While nitrification is thought to be the dominant pathway for marine N2O production, mechanisms remain unresolved. Previous studies have carried the implicit assumption that marine N2O originates directly from enzymatic sources. However, abiotic production of N2O is possible via chemical reactions between nitrogenous intermediates and redox active trace metals in <span class="hlt">seawater</span>. In this study, we investigated N2O production and isotopic composition in treatments with and without added hydroxylamine (NH2OH) and nitric oxide (NO), intermediates in microbial oxidation of ammonia to nitrite, and Fe(III). Addition of substrates to sterile artificial <span class="hlt">seawater</span> was compared with filtered and unfiltered <span class="hlt">seawater</span> from Sapelo Island, coastal Georgia, USA. N2O production was observed immediately after addition of Fe(III) in the presence of NH2OH at pH 8 in sterile artificial <span class="hlt">seawater</span>. Highest N2O production was observed in the presence of Fe(III), NO, and NH2OH. The isotopomer site preference of abiotically produced N2O was consistent with previous studies (31 ± 2 ‰). Higher abiotic N2O production was observed in sterile artificial <span class="hlt">seawater</span> (salinity: 35 ppt) than filtered Sapelo Island <span class="hlt">seawater</span> (salinity: 25 ppt) whereas diluted sterile artificial <span class="hlt">seawater</span> (18 ppt) showed lowest N2O production, suggesting that higher salinity promotes enhanced abiotic N2O production. Addition of Fe(III) to unfiltered Sapelo Island <span class="hlt">seawater</span> stimulated N2O production. The presence of ammonia-oxidizing archaea (AOA), which lack known N2O producing enzymes, in Sapelo Island <span class="hlt">seawater</span> was confirmed by successful amplification of the archaeal amoA gene, whereas ammonia-oxidizing bacteria (AOB), which contain N2O-producing enzymes were undetected. Given the few Fe-containing proteins present in AOA, it is likely that Fe(III) addition promoted N2O production via an abiotic vs. enzymatic N2O mechanism</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19850042373&hterms=glacier+melt&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D80%26Ntt%3Dglacier%2Bmelt','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19850042373&hterms=glacier+melt&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D80%26Ntt%3Dglacier%2Bmelt"><span><span class="hlt">Ice</span> sheet margins and <span class="hlt">ice</span> shelves</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Thomas, R. H.</p> <p>1984-01-01</p> <p>The effect of climate warming on the size of <span class="hlt">ice</span> sheet margins in polar regions is considered. Particular attention is given to the possibility of a rapid response to warming on the order of tens to hundreds of years. It is found that the early response of the polar regions to climate warming would be an increase in the area of summer melt on the <span class="hlt">ice</span> sheets and <span class="hlt">ice</span> shelves. For sufficiently large warming (5-10C) the delayed effects would include the breakup of the <span class="hlt">ice</span> shelves by an increase in <span class="hlt">ice</span> drainage rates, particularly from the <span class="hlt">ice</span> sheets. On the basis of published data for periodic changes in the thickness and melting rates of the marine <span class="hlt">ice</span> sheets and fjord glaciers in Greenland and Antarctica, it is shown that the rate of retreat (or advance) of an <span class="hlt">ice</span> sheet is primarily determined by: bedrock topography; the basal conditions of the grounded <span class="hlt">ice</span> sheet; and the <span class="hlt">ice</span> shelf condition downstream of the grounding line. A program of satellite and ground measurements to monitor the state of <span class="hlt">ice</span> sheet equilibrium is recommended.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18804655','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18804655"><span>Direct determination of uranium in <span class="hlt">seawater</span> by laser fluorimetry.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kumar, Sanjukta A; Shenoy, Niyoti S; Pandey, Shailaja; Sounderajan, Suvarna; Venkateswaran, G</p> <p>2008-10-19</p> <p>A method for estimation of uranium in <span class="hlt">seawater</span> by using steady state laser flourimetry is described. Uranium present in <span class="hlt">seawater</span>, in concentration of approximately 3 ng ml(-1) was estimated without prior separation of matrix. Quenching effect of major ions (Cl(-), Na(+), SO(4)(-), Mg(+), Ca(+), K(+), HCO(3)(-), Br(-)) present in <span class="hlt">seawater</span> on fluorescence intensity of uranium was studied. The concentration of phosphoric acid required for maximum enhancement of fluorescence intensity was optimized and was found to be 5%. Similarly the volume of concentrated nitric acid required to eliminate the quenching effect of chloride and bromide completely from 5 ml of <span class="hlt">seawater</span> were optimized and was found to be 3 ml. A simple equation was derived using steady state fluorescence correction method and was used for calculation of uranium concentration in <span class="hlt">seawater</span> samples. The method has a precesion of 1% (1s, n=3). The values obtained from laser fluorimetry were validated by analyzing the same samples by linear sweep adsorptive stripping voltametry (LSASV) of the uranium-chloranilic acid (2,5-dichloro-3,6-dihydroxy-1,4-benzoquinone) complex. Both the values are well in agreement.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017ChJOL..35..423L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017ChJOL..35..423L"><span>Corrosion performance of zinc coated steel in <span class="hlt">seawater</span> environment</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liu, Shuan; Zhao, Xia; Zhao, Haichao; Sun, Huyuan; Chen, Jianmin</p> <p>2017-03-01</p> <p>Considering the continuous exploitation of marine resources, it is very important to study the anticorrosion performance and durability of zinc coated streel (ZCS) because its increasing use as reinforcements in <span class="hlt">seawater</span>. Tafel polarization curves and linear polarization curves combined with electrochemical impedance spectroscopy (EIS) were employed to evaluate the corrosion performance of ZCS at Qingdao test station during long-term immersion in <span class="hlt">seawater</span>. The results indicated that the corrosion rate of the ZCS increased obviously with immersion time in <span class="hlt">seawater</span>. The corrosion products that formed on the zinc coated steel were loose and porous, and were mainly composed of Zn5(OH)8Cl2, Zn5(OH)6(CO3)2, and ZnO. Pitting corrosion occurred on the steel surface in neutral <span class="hlt">seawater</span>, and the rate of ZCS corrosion decreased with increasing pH.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19762103','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19762103"><span>Preparation of fungal conidia impacts their susceptibility to inactivation by ethanol <span class="hlt">vapours</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Dao, Thien; Dantigny, Philippe</p> <p>2009-11-15</p> <p>A common protocol employed for the preparation of conidia employs flooding a fungal colony grown on semi-solid media under optimum conditions with an aqueous solution. In contrast, conidia produced in a natural environment are usually not hydrated when disseminated in air and can be produced under water stress. In order to simulate the latter conditions, cultures were grown at different water activities and conidia were dry-harvested on the lid by turning the dishes upside-down then gently tapping the bottom of the box. This study aimed at assessing the effect of the preparation of fungal conidia on their inactivation by ethanol <span class="hlt">vapours</span>. Firstly ethanol <span class="hlt">vapours</span> (either 0.30 or 0.45 kPa) were applied to conidia obtained from the standardised protocol and to dry-harvested conidia for some species of Penicillium. While all dry-harvested conidia remained viable after 24 h of treatment, about 1.0, 3.5 and 2.5 log(10) reductions were observed for hydrated conidia of Penicillium chrysogenum, Penicillium digitatum and Penicillium italicum respectively. Secondly ethanol <span class="hlt">vapours</span> (0.67 kPa) were applied to dry-harvested conidia obtained from cultures grown at 0.99 a(w) and at reduced water activities. For all species, the susceptibility to ethanol <span class="hlt">vapours</span> of conidia obtained at 0.99 a(w) was significantly greater than that of conidia obtained at reduced water activities. Conidia produced in a natural environment under non-optimal conditions would be much more resistant to ethanol <span class="hlt">vapours</span> than those produced in the laboratory. This phenomenon may be due to a reduced intracellular water activity of dry-harvested conidia.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_12");'>12</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li class="active"><span>14</span></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_14 --> <div id="page_15" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="281"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1983EOSTr..64Q..97B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1983EOSTr..64Q..97B"><span>Mn solubility tested in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bell, Peter M.</p> <p></p> <p>It has been known for the past 2 or 3 years that the concentration of manganese in the upper several hundred meters of ocean water is unlike that of other trace metals such as copper, zinc, cadmium, and nickel. Trace metals are needed as a sort of ‘vitamin supplement’ by marine plants and animals; the surface supply is biologically scavenged and regenerated at depth. Thus ocean concentrations of trace metals increase with depth.Manganese, by contrast, appears to be concentrated in the photic zone and becomes relatively depleted in the depth interval 50-100 m from the surface. W. Landing and K. Bruland (Ear. Planet. Sci. Lett. 49, 45-56, 1980) described their observations of vertical distributions of manganese in a study of samples from the north Pacific. Recently, W. Sunda, S. A. Huntsman, and A. Harvey, in a study supported by the National Oceanic and Atmospheric Administration have found similar behavior of manganese in samples of coastal <span class="hlt">seawater</span> and offshore <span class="hlt">seawater</span> collected off North Carolina (Nature, 20, January 1983). They suggest on the basis of experiments conducted with these samples that the marine biological community itself serves to condition the surface <span class="hlt">seawater</span> and, with the assistance of photoreduction, cause manganese to dissolve in the otherwise oxygenated zones.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26PSL.481..316M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26PSL.481..316M"><span>Precipitation regime influence on oxygen triple-isotope distributions in Antarctic precipitation and <span class="hlt">ice</span> cores</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Miller, Martin F.</p> <p>2018-01-01</p> <p>The relative abundance of 17O in meteoric precipitation is usually reported in terms of the 17O-excess parameter. Variations of 17O-excess in Antarctic precipitation and <span class="hlt">ice</span> cores have hitherto been attributed to normalised relative humidity changes at the moisture source region, or to the influence of a temperature-dependent supersaturation-controlled kinetic isotope effect during in-cloud <span class="hlt">ice</span> formation below -20 °C. Neither mechanism, however, satisfactorily explains the large range of 17O-excess values reported from measurements. A different approach, based on the regression characteristics of 103 ln (1 +δ17 O) versus 103 ln (1 +δ18 O), is applied here to previously published isotopic data sets. The analysis indicates that clear-sky precipitation ('diamond dust'), which occurs widely in inland Antarctica, is characterised by an unusual relative abundance of 17O, distinct from that associated with cloud-derived, synoptic snowfall. Furthermore, this distinction appears to be largely preserved in the <span class="hlt">ice</span> core record. The respective mass contributions to snowfall accumulation - on both temporal and spatial scales - provides the basis of a simple, first-order explanation for the observed oxygen triple-isotope ratio variations in Antarctic precipitation, surface snow and <span class="hlt">ice</span> cores. Using this approach, it is shown that precipitation during the last major deglaciation, both in western Antarctica at the West Antarctic <span class="hlt">Ice</span> Sheet (WAIS) Divide and at Vostok on the eastern Antarctic plateau, consisted essentially of diamond dust only, despite a large temperature differential (and thus different water <span class="hlt">vapour</span> supersaturation conditions) at the two locations. In contrast, synoptic snowfall events dominate the accumulation record throughout the Holocene at both sites.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015BGeo...12.2131A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015BGeo...12.2131A"><span>Reconstruction of secular variation in <span class="hlt">seawater</span> sulfate concentrations</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Algeo, T. J.; Luo, G. M.; Song, H. Y.; Lyons, T. W.; Canfield, D. E.</p> <p>2015-04-01</p> <p>Long-term secular variation in <span class="hlt">seawater</span> sulfate concentrations ([SO42-]SW) is of interest owing to its relationship to the oxygenation history of Earth's surface environment. In this study, we develop two complementary approaches for quantification of sulfate concentrations in ancient <span class="hlt">seawater</span> and test their application to late Neoproterozoic (635 Ma) to Recent marine units. The "rate method" is based on two measurable parameters of paleomarine systems: (1) the S-isotope fractionation associated with microbial sulfate reduction (MSR), as proxied by Δ34SCAS-PY, and (2) the maximum rate of change in <span class="hlt">seawater</span> sulfate, as proxied by &partial; δ 34SCAS/∂ t(max). The "MSR-trend method" is based on the empirical relationship of Δ34SCAS-PY to aqueous sulfate concentrations in 81 modern depositional systems. For a given paleomarine system, the rate method yields an estimate of maximum possible [SO42-]SW (although results are dependent on assumptions regarding the pyrite burial flux, FPY), and the MSR-trend method yields an estimate of mean [SO42-]SW. An analysis of <span class="hlt">seawater</span> sulfate concentrations since 635 Ma suggests that [SO42-]SW was low during the late Neoproterozoic (<5 mM), rose sharply across the Ediacaran-Cambrian boundary (~5-10 mM), and rose again during the Permian (~10-30 mM) to levels that have varied only slightly since 250 Ma. However, Phanerozoic <span class="hlt">seawater</span> sulfate concentrations may have been drawn down to much lower levels (~1-4 mM) during short (<~2 Myr) intervals of the Cambrian, Early Triassic, Early Jurassic, and Cretaceous as a consequence of widespread ocean anoxia, intense MSR, and pyrite burial. The procedures developed in this study offer potential for future high-resolution quantitative analyses of paleo-<span class="hlt">seawater</span> sulfate concentrations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/21061702-inhibition-sodium-benzoate-stainless-steel-tropical-seawater','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/21061702-inhibition-sodium-benzoate-stainless-steel-tropical-seawater"><span>Inhibition of Sodium Benzoate on Stainless Steel in Tropical <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Seoh, S. Y.; Senin, H. B.; Nik, W. N. Wan</p> <p>2007-05-09</p> <p>The inhibition of sodium benzoate for stainless steel controlling corrosion was studied in <span class="hlt">seawater</span> at room temperature. Three sets of sample have been immersed in <span class="hlt">seawater</span> containing sodium benzoate with the concentrations of 0.3M, 0.6M and 1.0M respectively. One set of sample has been immersed in <span class="hlt">seawater</span> without adding any sodium benzoate. It was found that the highest corrosion rate was observed for the stainless steel with no inhibitor was added to the <span class="hlt">seawater</span>. As the concentration of sodium benzoate being increased, the corrosion rate is decreases. Results show that by the addition of 1.0M of sodium benzoate in seawatermore » samples, it giving {>=} 90% efficiencies.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21248050','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21248050"><span>Effect of drilling fluid systems and temperature on oil mist and <span class="hlt">vapour</span> levels generated from shale shaker.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Steinsvåg, Kjersti; Galea, Karen S; Krüger, Kirsti; Peikli, Vegard; Sánchez-Jiménez, Araceli; Sætvedt, Esther; Searl, Alison; Cherrie, John W; van Tongeren, Martie</p> <p>2011-05-01</p> <p>Workers in the drilling section of the offshore petroleum industry are exposed to air pollutants generated by drilling fluids. Oil mist and oil <span class="hlt">vapour</span> concentrations have been measured in the drilling fluid processing areas for decades; however, little work has been carried out to investigate exposure determinants such as drilling fluid viscosity and temperature. A study was undertaken to investigate the effect of two different oil-based drilling fluid systems and their temperature on oil mist, oil <span class="hlt">vapour</span>, and total volatile organic compounds (TVOC) levels in a simulated shale shaker room at a purpose-built test centre. Oil mist and oil <span class="hlt">vapour</span> concentrations were sampled simultaneously using a sampling arrangement consisting of a Millipore closed cassette loaded with glass fibre and cellulose acetate filters attached to a backup charcoal tube. TVOCs were measured by a PhoCheck photo-ionization detector direct reading instrument. Concentrations of oil mist, oil <span class="hlt">vapour</span>, and TVOC in the atmosphere surrounding the shale shaker were assessed during three separate test periods. Two oil-based drilling fluids, denoted 'System 2.0' and 'System 3.5', containing base oils with a viscosity of 2.0 and 3.3-3.7 mm(2) s(-1) at 40°C, respectively, were used at temperatures ranging from 40 to 75°C. In general, the System 2.0 yielded low oil mist levels, but high oil <span class="hlt">vapour</span> concentrations, while the opposite was found for the System 3.5. Statistical significant differences between the drilling fluid systems were found for oil mist (P = 0.025),<span class="hlt">vapour</span> (P < 0.001), and TVOC (P = 0.011). Increasing temperature increased the oil mist, oil <span class="hlt">vapour</span>, and TVOC levels. Oil <span class="hlt">vapour</span> levels at the test facility exceeded the Norwegian oil <span class="hlt">vapour</span> occupational exposure limit (OEL) of 30 mg m(-3) when the drilling fluid temperature was ≥50°C. The practice of testing compliance of oil <span class="hlt">vapour</span> exposure from drilling fluids systems containing base oils with viscosity of ≤2.0 mm(2) s(-1) at 40</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.A32C..05D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.A32C..05D"><span>Measurements to Fill Knowledge Gaps on <span class="hlt">Ice</span> Nucleating Particle Sources over Oceans</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>DeMott, P. J.; Hill, T. C.; Ruppel, M. J.; Prather, K. A.; Collins, D. B.; Axson, J. L.; Lee, T.; Hwang, C. Y.; Sullivan, R. C.; McMeeking, G. R.; Mason, R.; Bertram, A. K.; Mayol-Bracero, O. L.; Lewis, E. R.</p> <p>2013-12-01</p> <p>Measurements of the temperature spectrum of <span class="hlt">ice</span> nucleating particle concentrations by two methods in recent specialized laboratory sea spray studies and field campaigns in the Northern Hemisphere will be discussed and compared with historical data from over Southern Oceans. In general, new measurements of the condensation/immersion freezing activation spectra of realistically-generated laboratory sea spray particles (by wave generation or plunging water bubble production) are consistent with previous measurements made over oceans. The number concentrations of <span class="hlt">ice</span> nuclei tend to be lower than are measured over land regions, at least for modestly supercooled cloud conditions. Certain but complex connections of <span class="hlt">ice</span> nucleating particle production to ocean microbiological processes affecting the chemical composition of the sea surface microlayer are seen, but the nature of the <span class="hlt">ice</span> nucleating units of particles remains to be identified. Associations of <span class="hlt">ice</span> nucleating particle concentrations with heterotrophic bacterial concentrations were noted in some experiments, while correlation with chlorophyll-a concentration in <span class="hlt">seawater</span> was clearly identified in laboratory simulations of phytoplankton blooms. These data may ultimately serve as the basis for parameterization development for <span class="hlt">ice</span> initiation in numerical model simulations of mixed-phase clouds. Atmospheric measurements have been made at island sites, via aircraft, and from ship-based filter collections in the Northern Hemisphere. The immersion freezing spectra of these particles are similar to those found in recent laboratory studies and historical measurements, but show the expected natural variability by location. The majority of particles detected thus far as <span class="hlt">ice</span> nuclei from sea spray and in marine air show minimal or episodic/variable direct participation of biological <span class="hlt">ice</span> nucleating organisms on the basis of sensitivity to high temperatures (95°C). However, assembled measurements are still sparse, the nuclei</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/11267747','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/11267747"><span>Solvent <span class="hlt">vapour</span> monitoring in work space by solid phase micro extraction.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Li, K; Santilli, A; Goldthorp, M; Whiticar, S; Lambert, P; Fingas, M</p> <p>2001-05-07</p> <p>Solid phase micro extraction (SPME) is a fast, solvent-less alternative to conventional charcoal tube sampling/carbon disulfide extraction for volatile organic compounds (VOC). In this work, SPME was compared to the active sampling technique in a typical lab atmosphere. Two different types of fibre coatings were evaluated for solvent <span class="hlt">vapour</span> at ambient concentration. A general purpose 100 microm film polydimethylsiloxane (PDMS) fibre was found to be unsuitable for VOC work, despite the thick coating. The mixed-phase carboxen/PDMS fibre was found to be suitable. Sensitivity of the SPME was far greater than charcoal sorbent tube method. Calibration studies using typical solvent such as dichloromethane (DCM), benzene (B) and toluene (T) showed an optimal exposure time of 5 min, with a repeatability of less than 20% for a broad spectrum of organic <span class="hlt">vapour</span>. Minimum detectable amount for DCM is in the range of 0.01 microg/l (0.003 ppmv). Variation among different fibres was generally within 30% at a <span class="hlt">vapour</span> concentration of 1 microg DCM/l, which was more than adequate for field monitoring purpose. Adsorption characteristics and calibration procedures were studied. An actual application of SPME was carried out to measure background level of solvent <span class="hlt">vapour</span> at a bench where DCM was used extensively. Agreement between the SPME and the charcoal sampling method was generally within a factor of two. No DCM concentration was found to be above the regulatory limit of 50 ppmv.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26900179','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26900179"><span>Metrological challenges for measurements of key climatological observables: Oceanic salinity and pH, and atmospheric humidity. Part 1: Overview.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Feistel, R; Wielgosz, R; Bell, S A; Camões, M F; Cooper, J R; Dexter, P; Dickson, A G; Fisicaro, P; Harvey, A H; Heinonen, M; Hellmuth, O; Kretzschmar, H-J; Lovell-Smith, J W; McDougall, T J; Pawlowicz, R; Ridout, P; Seitz, S; Spitzer, P; Stoica, D; Wolf, H</p> <p>2016-02-01</p> <p>Water in its three ambient phases plays the central thermodynamic role in the terrestrial climate system. Clouds control Earth's radiation balance, atmospheric water <span class="hlt">vapour</span> is the strongest "greenhouse" gas, and non-equilibrium relative humidity at the air-sea interface drives evaporation and latent heat export from the ocean. On climatic time scales, melting <span class="hlt">ice</span> caps and regional deviations of the hydrological cycle result in changes of <span class="hlt">seawater</span> salinity, which in turn may modify the global circulation of the oceans and their ability to store heat and to buffer anthropogenically produced carbon dioxide. In this paper, together with three companion articles, we examine the climatologically relevant quantities ocean salinity, <span class="hlt">seawater</span> pH and atmospheric relative humidity, noting fundamental deficiencies in the definitions of those key observables, and their lack of secure foundation on the International System of Units, the SI. The metrological histories of those three quantities are reviewed, problems with their current definitions and measurement practices are analysed, and options for future improvements are discussed in conjunction with the recent <span class="hlt">seawater</span> standard TEOS-10. It is concluded that the International Bureau of Weights and Measures, BIPM, in cooperation with the International Association for the Properties of Water and Steam, IAPWS, along with other international organisations and institutions, can make significant contributions by developing and recommending state-of-the-art solutions for these long standing metrological problems in climatology.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016Metro..53R...1F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016Metro..53R...1F"><span>Metrological challenges for measurements of key climatological observables: oceanic salinity and pH, and atmospheric humidity. Part 1: overview</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Feistel, R.; Wielgosz, R.; Bell, S. A.; Camões, M. F.; Cooper, J. R.; Dexter, P.; Dickson, A. G.; Fisicaro, P.; Harvey, A. H.; Heinonen, M.; Hellmuth, O.; Kretzschmar, H.-J.; Lovell-Smith, J. W.; McDougall, T. J.; Pawlowicz, R.; Ridout, P.; Seitz, S.; Spitzer, P.; Stoica, D.; Wolf, H.</p> <p>2016-02-01</p> <p>Water in its three ambient phases plays the central thermodynamic role in the terrestrial climate system. Clouds control Earth’s radiation balance, atmospheric water <span class="hlt">vapour</span> is the strongest ‘greenhouse’ gas, and non-equilibrium relative humidity at the air-sea interface drives evaporation and latent heat export from the ocean. On climatic time scales, melting <span class="hlt">ice</span> caps and regional deviations of the hydrological cycle result in changes of <span class="hlt">seawater</span> salinity, which in turn may modify the global circulation of the oceans and their ability to store heat and to buffer anthropogenically produced carbon dioxide. In this paper, together with three companion articles, we examine the climatologically relevant quantities ocean salinity, <span class="hlt">seawater</span> pH and atmospheric relative humidity, noting fundamental deficiencies in the definitions of those key observables, and their lack of secure foundation on the International System of Units, the SI. The metrological histories of those three quantities are reviewed, problems with their current definitions and measurement practices are analysed, and options for future improvements are discussed in conjunction with the recent <span class="hlt">seawater</span> standard TEOS-10. It is concluded that the International Bureau of Weights and Measures, BIPM, in cooperation with the International Association for the Properties of Water and Steam, IAPWS, along with other international organizations and institutions, can make significant contributions by developing and recommending state-of-the-art solutions for these long standing metrological problems in climatology.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008AGUFMED33A0619H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008AGUFMED33A0619H"><span><span class="hlt">Ice</span>, <span class="hlt">Ice</span>, Baby!</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hamilton, C.</p> <p>2008-12-01</p> <p>The Center for Remote Sensing of <span class="hlt">Ice</span> Sheets (CReSIS) has developed an outreach program based on hands-on activities called "<span class="hlt">Ice</span>, <span class="hlt">Ice</span>, Baby". These lessons are designed to teach the science principles of displacement, forces of motion, density, and states of matter. These properties are easily taught through the interesting topics of glaciers, icebergs, and sea level rise in K-8 classrooms. The activities are fun, engaging, and simple enough to be used at science fairs and family science nights. Students who have participated in "<span class="hlt">Ice</span>, <span class="hlt">Ice</span>, Baby" have successfully taught these to adults and students at informal events. The lessons are based on education standards which are available on our website www.cresis.ku.edu. This presentation will provide information on the activities, survey results from teachers who have used the material, and other suggested material that can be used before and after the activities.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1154652','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1154652"><span>Uranium from <span class="hlt">Seawater</span> Program Review; Fuel Resources Uranium from <span class="hlt">Seawater</span> Program DOE Office of Nuclear Energy</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>None</p> <p>2013-07-01</p> <p>For nuclear energy to remain sustainable in the United States, economically viable sources of uranium beyond terrestrial ores must be developed. The goal of this program is to develop advanced adsorbents that can extract uranium from <span class="hlt">seawater</span> at twice the capacity of the best adsorbent developed by researchers at the Japan Atomic Energy Agency (JAEA), 1.5 mg U/g adsorbent. A multidisciplinary team from Oak Ridge National Laboratory, Lawrence Berkeley National Laboratory, Pacific Northwest National Laboratory, and the University of Texas at Austin was assembled to address this challenging problem. Polymeric adsorbents, based on the radiation grafting of acrylonitrile and methacrylicmore » acid onto high surface-area polyethylene fibers followed by conversion of the nitriles to amidoximes, have been developed. These poly(acrylamidoxime-co-methacrylic acid) fibers showed uranium adsorption capacities for the extraction of uranium from <span class="hlt">seawater</span> that exceed 3 mg U/g adsorbent in testing at the Pacific Northwest National Laboratory Marine Sciences Laboratory. The essence of this novel technology lies in the unique high surface-area trunk material that considerably increases the grafting yield of functional groups without compromising its mechanical properties. This technology received an R&D100 Award in 2012. In addition, high surface area nanomaterial adsorbents are under development with the goal of increasing uranium adsorption capacity by taking advantage of the high surface areas and tunable porosity of carbon-based nanomaterials. Simultaneously, de novo structure-based computational design methods are being used to design more selective and stable ligands and the most promising candidates are being synthesized, tested and evaluated for incorporation onto a support matrix. Fundamental thermodynamic and kinetic studies are being carried out to improve the adsorption efficiency, the selectivity of uranium over other metals, and the stability of the adsorbents</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5624506','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5624506"><span>Magnesium isotope evidence that accretional <span class="hlt">vapour</span> loss shapes planetary compositions</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Hin, Remco C.; Coath, Christopher D.; Carter, Philip J.; Nimmo, Francis; Lai, Yi-Jen; Pogge von Strandmann, Philip A.E.; Willbold, Matthias; Leinhardt, Zoë M.; Walter, Michael J.; Elliott, Tim</p> <p>2017-01-01</p> <p>It has long been recognised that Earth and other differentiated planetary bodies are chemically fractionated compared to primitive, chondritic meteorites and by inference the primordial disk from which they formed. An important question has been whether the notable volatile depletions of planetary bodies are a consequence of accretion1, or inherited from prior nebular fractionation2. The isotopic compositions of the main constituents of planetary bodies can contribute to this debate3–6. Using a new analytical approach to address key issues of accuracy inherent in conventional methods, we show that all differentiated bodies have isotopically heavier magnesium compositions than chondritic meteorites. We argue that possible magnesium isotope fractionation during condensation of the solar nebula, core formation and silicate differentiation cannot explain these observations. However, isotopic fractionation between liquid and <span class="hlt">vapour</span> followed by <span class="hlt">vapour</span> escape during accretionary growth of planetesimals generates appropriate residual compositions. Our modelling implies that the isotopic compositions of Mg, Si and Fe and the relative abundances of the major elements of Earth, and other planetary bodies, are a natural consequence of substantial (~40% by mass) <span class="hlt">vapour</span> loss from growing planetesimals by this mechanism. PMID:28959965</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1693281','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1693281"><span>Land cover change and water <span class="hlt">vapour</span> flows: learning from Australia.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Gordon, Line; Dunlop, Michael; Foran, Barney</p> <p>2003-01-01</p> <p>Australia is faced with large-scale dryland salinization problems, largely as a consequence of the clearing of native vegetation for cropland and grassland. We estimate the change in continental water <span class="hlt">vapour</span> flow (evapotranspiration) of Australia during the past 200 years. During this period there has been a substantial decrease in woody vegetation and a corresponding increase in croplands and grasslands. The shift in land use has caused a ca. 10% decrease in water <span class="hlt">vapour</span> flows from the continent. This reduction corresponds to an annual freshwater flow of almost 340 km(3). The society-induced alteration of freshwater flows is estimated at more than 15 times the volume of run-off freshwater that is diverted and actively managed in the Australian society. These substantial water <span class="hlt">vapour</span> flow alterations were previously not addressed in water management but are now causing serious impacts on the Australian society and local economies. Global and continental freshwater assessments and policy often neglects the interplay between freshwater flows and landscape dynamics. Freshwater issues on both regional and global levels must be rethought and the interplay between terrestrial ecosystems and freshwater better incorporated in freshwater and ecosystem management. PMID:14728792</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.H23E1589L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.H23E1589L"><span>Opportunities and Barriers to Address <span class="hlt">Seawater</span> Intrusion Along California's Coast</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Langridge, R.</p> <p>2016-12-01</p> <p>In many California coastal areas reliant on groundwater <span class="hlt">seawater</span> intrusion is a serious problem. This presentation will discuss how particular groundwater management institutions in the state are addressing <span class="hlt">seawater</span> intrusion issues, how stakeholders are participating in this process, and how scientific information can contribute to policies that support reducing or halting ongoing intrusion. In 2014, the California Legislature passed the Sustainable Groundwater Management Act (SGMA). The Act established requirements for 127 high and medium priority groundwater basins to form groundwater sustainability agencies (GSAs) and develop plans to sustainably manage their basin. Sustainable is defined in SGMA as avoiding specific unacceptable impacts, including significant and unreasonable <span class="hlt">seawater</span> intrusion. Special Act Districts, created by an act of the legislature, have the option to be the sole GSA in their service area, and they can provide a window into current and potentially future strategies to address <span class="hlt">seawater</span> intrusion. Additionally, adjudicated basins are often considered one of the best approaches to achieve efficient groundwater management, and these basins are exempt from SGMA and managed pursuant to a court judgment. The strategies utilized to manage <span class="hlt">seawater</span> intrusion by three special act districts and five adjudicated basins will be discussed. These basins cover significant areas of central and southern California and all have experienced <span class="hlt">seawater</span> intrusion. Our research team just completed reports for the State Water Resources Control Board on all the adjudicated and special act districts in the state, and this presentation will draw on our findings to better understand the barriers and opportunities to alleviate <span class="hlt">seawater</span> intrusion and the information required to develop solutions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018E%26ES..153c2021L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018E%26ES..153c2021L"><span>Review of vortex tube expansion in <span class="hlt">vapour</span> compression refrigeration system</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liu, Yefeng; Yu, Jun</p> <p>2018-05-01</p> <p>A vortex tube expansion device replacing the throttle valve is proposed to improve the efficiency of <span class="hlt">vapour</span> compression refrigeration cycle by reducing the loss of irreversibility in expansion process. The vortex tube is well-suited for these applications because it is simple, compact, light, quiet. Thus, this paper presents an overview of the thermodynamic analysis of <span class="hlt">vapour</span> compression refrigeration cycle with vortex tube expansion device using different refrigerants. The paper also reviews the experiments and the calculations presented in previous studies on temperature separation in the vortex tube. The temperature separation mechanism and the flow-field inside the vortex tubes is explored by measuring the pressure, velocity, and temperature fields.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016PCE....94...56F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016PCE....94...56F"><span>On the relationship between atmospheric water <span class="hlt">vapour</span> transport and extra-tropical cyclones development</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ferreira, Juan A.; Liberato, Margarida L. R.; Ramos, Alexandre M.</p> <p>2016-08-01</p> <p>In this study we seek to investigate the role of atmospheric water <span class="hlt">vapour</span> on the intensification of extra-tropical cyclones over the North Atlantic Ocean and more specifically to investigate the linkage between atmospheric rivers' conditions leading to the explosive development of extra-tropical cyclones. Several WRF-ARW simulations for three recent extra-tropical storms that had major negative socio-economic impacts in the Iberian Peninsula and south-western Europe (Klaus, 2009; Gong, 2013 and Stephanie, 2014) are performed in which the water <span class="hlt">vapour</span> content of the initial and boundary conditions are tuned. Analyses of the vertically integrated <span class="hlt">vapour</span> transport show the dependence of the storms' development on atmospheric water <span class="hlt">vapour</span>. In addition, results also show changes in the shape of the jet stream resulting in a reduction of the upper wind divergence, which in turn affects the intensification of the extra-tropical cyclones studied. This study suggests that atmospheric rivers tend to favour the conditions for explosive extra-tropical storms' development in the three case studies, as simulations performed without the existence of atmospheric rivers produce shallow mid-latitude cyclones, that is, cyclones that are not so intense as those on the reference simulations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26887494','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26887494"><span><span class="hlt">Ice</span> stream activity scaled to <span class="hlt">ice</span> sheet volume during Laurentide <span class="hlt">Ice</span> Sheet deglaciation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stokes, C R; Margold, M; Clark, C D; Tarasov, L</p> <p>2016-02-18</p> <p>The contribution of the Greenland and West Antarctic <span class="hlt">ice</span> sheets to sea level has increased in recent decades, largely owing to the thinning and retreat of outlet glaciers and <span class="hlt">ice</span> streams. This dynamic loss is a serious concern, with some modelling studies suggesting that the collapse of a major <span class="hlt">ice</span> sheet could be imminent or potentially underway in West Antarctica, but others predicting a more limited response. A major problem is that observations used to initialize and calibrate models typically span only a few decades, and, at the <span class="hlt">ice</span>-sheet scale, it is unclear how the entire drainage network of <span class="hlt">ice</span> streams evolves over longer timescales. This represents one of the largest sources of uncertainty when predicting the contributions of <span class="hlt">ice</span> sheets to sea-level rise. A key question is whether <span class="hlt">ice</span> streams might increase and sustain rates of mass loss over centuries or millennia, beyond those expected for a given ocean-climate forcing. Here we reconstruct the activity of 117 <span class="hlt">ice</span> streams that operated at various times during deglaciation of the Laurentide <span class="hlt">Ice</span> Sheet (from about 22,000 to 7,000 years ago) and show that as they activated and deactivated in different locations, their overall number decreased, they occupied a progressively smaller percentage of the <span class="hlt">ice</span> sheet perimeter and their total discharge decreased. The underlying geology and topography clearly influenced <span class="hlt">ice</span> stream activity, but--at the <span class="hlt">ice</span>-sheet scale--their drainage network adjusted and was linked to changes in <span class="hlt">ice</span> sheet volume. It is unclear whether these findings can be directly translated to modern <span class="hlt">ice</span> sheets. However, contrary to the view that sees <span class="hlt">ice</span> streams as unstable entities that can accelerate <span class="hlt">ice</span>-sheet deglaciation, we conclude that <span class="hlt">ice</span> streams exerted progressively less influence on <span class="hlt">ice</span> sheet mass balance during the retreat of the Laurentide <span class="hlt">Ice</span> Sheet.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=44182&Lab=ORD&keyword=zika&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=44182&Lab=ORD&keyword=zika&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>REACTION PRODUCTS FROM THE CHLORINATION OF <span class="hlt">SEAWATER</span>. CHAPTER 34</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>Much of the present information on the products formed when <span class="hlt">seawater</span> is chlorinated is based on observations of laboratory experiments in which chlorine was added to <span class="hlt">seawater</span> to stimulate conditions of electricity generating plants. Results are reported for a field study at the P...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70030122','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70030122"><span>Quasi-horizontal circulation cells in 3D <span class="hlt">seawater</span> intrusion</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Abarca, E.; Carrera, J.; Sanchez-Vila, X.; Voss, C.I.</p> <p>2007-01-01</p> <p>The <span class="hlt">seawater</span> intrusion process is characterized by the difference in freshwater and <span class="hlt">seawater</span> density that causes freshwater to float on <span class="hlt">seawater</span>. Many confined aquifers have a large horizontal extension with respect to thickness. In these cases, while buoyancy acts in the vertical direction, flow is confined between the upper and bottom boundaries and the effect of gravity is controlled by variations of aquifer elevation. Therefore, the effective gravity is controlled by the slope and the shape of the aquifer boundaries. Variability in the topography of the aquifer boundaries is one case where 3D analysis is necessary. In this work, density-dependent flow processes caused by 3D aquifer geometry are studied numerically and specifically, considering a lateral slope of the aquifer boundaries. Sub-horizontal circulation cells are formed in the saltwater entering the aquifer. The penetration of the saltwater can be quantified by a dimensionless buoyancy number that measures the lateral slope of the aquifer relative to freshwater flux. The penetration of the <span class="hlt">seawater</span> intrusion wedge is controlled more by this slope than by the aquifer thickness and dispersivity. Thus, the slope must be taken into account in order to accurately evaluate <span class="hlt">seawater</span> intrusion. ?? 2007 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27019007','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27019007"><span>Graphene-based Recyclable Photo-Absorbers for High-Efficiency <span class="hlt">Seawater</span> Desalination.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Wang, Xiangqing; Ou, Gang; Wang, Ning; Wu, Hui</p> <p>2016-04-13</p> <p>Today's scientific advances in water desalination dramatically increase our ability to transform <span class="hlt">seawater</span> into fresh water. As an important source of renewable energy, solar power holds great potential to drive the desalination of <span class="hlt">seawater</span>. Previously, solar assisted evaporation systems usually relied on highly concentrated sunlight or were not suitable to treat <span class="hlt">seawater</span> or wastewater, severely limiting the large scale application of solar evaporation technology. Thus, a new strategy is urgently required in order to overcome these problems. In this study, we developed a solar thermal evaporation system based on reduced graphene oxide (rGO) decorated with magnetic nanoparticles (MNPs). Because this material can absorb over 95% of sunlight, we achieved high evaporation efficiency up to 70% under only 1 kW m(-2) irradiation. Moreover, it could be separated from <span class="hlt">seawater</span> under the action of magnetic force by decorated with MNPs. Thus, this system provides an advantage of recyclability, which can significantly reduce the material consumptions. Additionally, by using photoabsorbing bulk or layer materials, the deposition of solutes offen occurs in pores of materials during <span class="hlt">seawater</span> desalination, leading to the decrease of efficiency. However, this problem can be easily solved by using MNPs, which suggests this system can be used in not only pure water system but also high-salinity wastewater system. This study shows good prospects of graphene-based materials for <span class="hlt">seawater</span> desalination and high-salinity wastewater treatment.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_13");'>13</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li class="active"><span>15</span></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_15 --> <div id="page_16" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="301"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014JGRG..119.2276G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014JGRG..119.2276G"><span>Organic iodine in Antarctic sea <span class="hlt">ice</span>: A comparison between winter in the Weddell Sea and summer in the Amundsen Sea</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Granfors, Anna; Ahnoff, Martin; Mills, Matthew M.; Abrahamsson, Katarina</p> <p>2014-12-01</p> <p>Recent studies have recognized sea <span class="hlt">ice</span> as a source of reactive iodine to the Antarctic boundary layer. Volatile iodinated compounds (iodocarbons) are released from sea <span class="hlt">ice</span>, and they have been suggested to contribute to the formation of iodine oxide (IO), which takes part in tropospheric ozone destruction in the polar spring. We measured iodocarbons (CH3I, CH2ClI, CH2BrI, and CH2I2) in sea <span class="hlt">ice</span>, snow, brine, and air during two expeditions to Antarctica, OSO 10/11 to the Amundsen Sea during austral summer and ANT XXIX/6 to the Weddell Sea in austral winter. These are the first reported measurements of iodocarbons from the Antarctic winter. Iodocarbons were enriched in sea <span class="hlt">ice</span> in relation to <span class="hlt">seawater</span> in both summer and winter. During summer, the positive relationship to chlorophyll a biomass indicated a biological origin. We suggest that CH3I is formed biotically in sea <span class="hlt">ice</span> during both summer and winter. For CH2ClI, CH2BrI, and CH2I2, an additional abiotic source at the snow/<span class="hlt">ice</span> interface in winter is suggested. Elevated air concentrations of CH3I and CH2ClI during winter indicate that they are enriched in lower troposphere and may take part in the formation of IO at polar sunrise.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPhCS.891a2009S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPhCS.891a2009S"><span>Numerical Simulation of Pulsation Flow in the <span class="hlt">Vapour</span> Channel of Short Low Temperature Heat Pipes at High Heat Loads</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Seryakov, A. V.; Konkin, A. V.</p> <p>2017-11-01</p> <p>The results of the numerical simulation of pulsations in the Laval-liked <span class="hlt">vapour</span> channel of short low-temperature range heat pipes (HPs) are presented. The numerical results confirmed the experimentally obtained increase of the frequency of pulsations in the <span class="hlt">vapour</span> channel of short HPs with increasing overheat of the porous evaporator relative to the boiling point of the working fluid. The occurrence of pressure pulsations inside the <span class="hlt">vapour</span> channel in a short HPs is a complex phenomenon associated with the boiling beginning in the capillary-porous evaporator at high heat loads, and appearance the excess amount of <span class="hlt">vapour</span> above it, leading to the increase in pressure P to a value at which the boiling point TB of the working fluid becomes higher than the evaporator temperature Tev. <span class="hlt">Vapour</span> clot spreads through the <span class="hlt">vapour</span> channel and condense, and then a rarefaction wave return from condenser in the evaporator, the boiling in which is resumed and the next cycle of the pulsations is repeated. Numerical simulation was performed using finite element method implemented in the commercial program ANSYS Multiphisics 14.5 in the two-dimensional setting of axis symmetric moist <span class="hlt">vapour</span> flow with third kind boundary conditions.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010JPhD...43Q4009T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010JPhD...43Q4009T"><span>Time-dependent calculations of molten pool formation and thermal plasma with metal <span class="hlt">vapour</span> in gas tungsten arc welding</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Tanaka, M.; Yamamoto, K.; Tashiro, S.; Nakata, K.; Yamamoto, E.; Yamazaki, K.; Suzuki, K.; Murphy, A. B.; Lowke, J. J.</p> <p>2010-11-01</p> <p>A gas tungsten arc (GTA) was modelled taking into account the contamination of the plasma by metal <span class="hlt">vapour</span> from the molten anode. The whole region of GTA atmosphere including the tungsten cathode, the arc plasma and the anode was treated using a unified numerical model. A viscosity approximation was used to express the diffusion coefficient in terms of viscosity of the shielding gas and metal <span class="hlt">vapour</span>. The transient two-dimensional distributions of temperature, velocity of plasma flow and iron <span class="hlt">vapour</span> concentration were predicted, together with the molten pool as a function of time for a 150 A arc current at atmospheric pressure, both for helium and argon gases. It was shown that the thermal plasma in the GTA was influenced by iron <span class="hlt">vapour</span> from the molten pool surface and that the concentration of iron <span class="hlt">vapour</span> in the plasma was dependent on the temperature of the molten pool. GTA on high sulfur stainless steel was calculated to discuss the differences between a low sulfur and a high sulfur stainless steel anode. Helium was selected as the shielding gas because a helium GTA produces more metal <span class="hlt">vapour</span> than an argon GTA. In the GTA on a high sulfur stainless steel anode, iron <span class="hlt">vapour</span> and current path were constricted. Radiative emission density in the GTA on high sulfur stainless steel was also concentrated in the centre area of the arc plasma together with the iron <span class="hlt">vapour</span> although the temperature distributions were almost the same as that in the case of a low sulfur stainless steel anode.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-200910220009HQ.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-200910220009HQ.html"><span><span class="hlt">Ice</span> Bridge Antarctic Sea <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2009-10-21</p> <p>An iceberg is seen out the window of NASA's DC-8 research aircraft as it flies 2,000 feet above the Amundsen Sea in West Antarctica on Wednesday, Oct., 21, 2009. This was the fourth science flight of NASA‚Äôs Operation <span class="hlt">Ice</span> Bridge airborne Earth science mission to study Antarctic <span class="hlt">ice</span> sheets, sea <span class="hlt">ice</span>, and <span class="hlt">ice</span> shelves. Photo Credit: (NASA/Jane Peterson)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24489821','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24489821"><span>The response of Antarctic sea <span class="hlt">ice</span> algae to changes in pH and CO2.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>McMinn, Andrew; Müller, Marius N; Martin, Andrew; Ryan, Ken G</p> <p>2014-01-01</p> <p>Ocean acidification substantially alters ocean carbon chemistry and hence pH but the effects on sea <span class="hlt">ice</span> formation and the CO2 concentration in the enclosed brine channels are unknown. Microbial communities inhabiting sea <span class="hlt">ice</span> ecosystems currently contribute 10-50% of the annual primary production of polar seas, supporting overwintering zooplankton species, especially Antarctic krill, and seeding spring phytoplankton blooms. Ocean acidification is occurring in all surface waters but the strongest effects will be experienced in polar ecosystems with significant effects on all trophic levels. Brine algae collected from McMurdo Sound (Antarctica) sea <span class="hlt">ice</span> was incubated in situ under various carbonate chemistry conditions. The carbon chemistry was manipulated with acid, bicarbonate and bases to produce a pCO2 and pH range from 238 to 6066 µatm and 7.19 to 8.66, respectively. Elevated pCO2 positively affected the growth rate of the brine algal community, dominated by the unique <span class="hlt">ice</span> dinoflagellate, Polarella glacialis. Growth rates were significantly reduced when pH dropped below 7.6. However, when the pH was held constant and the pCO2 increased, growth rates of the brine algae increased by more than 20% and showed no decline at pCO2 values more than five times current ambient levels. We suggest that projected increases in <span class="hlt">seawater</span> pCO2, associated with OA, will not adversely impact brine algal communities.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018AIPC.1958b0006I','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018AIPC.1958b0006I"><span><span class="hlt">Seawater</span> infiltration effect on thermal degradation of fiber reinforced epoxy composites</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ibrahim, Mohd Haziq Izzuddin bin; Hassan, Mohamad Zaki bin; Ibrahim, Ikhwan; Rashidi, Ahmad Hadi Mohamed; Nor, Siti Fadzilah M.; Daud, Mohd Yusof Md</p> <p>2018-05-01</p> <p><span class="hlt">Seawater</span> salinity has been associated with the reduction of polymer structure durability. The aim of this study is to investigate the change in thermal degradation of fiber reinforced epoxy composite due to the presence of <span class="hlt">seawater</span>. Carbon fiber, carbon/kevlar, fiberglass, and jute that reinforced with epoxy resin was laminated through hand-layup technique. Initially, these specimen was sectioned to 5×5 mm dimension, then immersed in <span class="hlt">seawater</span> and distilled water at room temperature until it has thoroughly saturated. Following, the thermal degradation analysis using Differential Scanning Calorimetry (DSC), the thermic changes due to <span class="hlt">seawater</span> infiltration was defined. The finding shows that moisture absorption reduces the glass transition temperature (Tg) of fiber reinforced epoxy composite. However, the glass transition temperature (Tg) of <span class="hlt">seawater</span> infiltrated laminate composite is compareable with distilled water infiltrated laminate composite. The carbon fiber reinfored epoxy has the highest glass transition temperature out of all specimen.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014HESS...18.1663M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014HESS...18.1663M"><span>Intensively exploited Mediterranean aquifers: resilience to <span class="hlt">seawater</span> intrusion and proximity to critical thresholds</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Mazi, K.; Koussis, A. D.; Destouni, G.</p> <p>2014-05-01</p> <p>We investigate <span class="hlt">seawater</span> intrusion in three prominent Mediterranean aquifers that are subject to intensive exploitation and modified hydrologic regimes by human activities: the Nile Delta, Israel Coastal and Cyprus Akrotiri aquifers. Using a generalized analytical sharp interface model, we review the salinization history and current status of these aquifers, and quantify their resilience/vulnerability to current and future <span class="hlt">seawater</span> intrusion forcings. We identify two different critical limits of <span class="hlt">seawater</span> intrusion under groundwater exploitation and/or climatic stress: a limit of well intrusion, at which intruded <span class="hlt">seawater</span> reaches key locations of groundwater pumping, and a tipping point of complete <span class="hlt">seawater</span> intrusion up to the prevailing groundwater divide of a coastal aquifer. Either limit can be reached, and ultimately crossed, under intensive aquifer exploitation and/or climate-driven change. We show that <span class="hlt">seawater</span> intrusion vulnerability for different aquifer cases can be directly compared in terms of normalized intrusion performance curves. The site-specific assessments show that (a) the intruding <span class="hlt">seawater</span> currently seriously threatens the Nile Delta aquifer, (b) in the Israel Coastal aquifer the sharp interface toe approaches the well location and (c) the Cyprus Akrotiri aquifer is currently somewhat less threatened by increased <span class="hlt">seawater</span> intrusion.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JGRC..123.2192D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JGRC..123.2192D"><span>Uncertainties in Climatological <span class="hlt">Seawater</span> Density Calculations</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Dai, Hao; Zhang, Xining</p> <p>2018-03-01</p> <p>In most applications, with <span class="hlt">seawater</span> conductivity, temperature, and pressure data measured in situ by various observation instruments e.g., Conductivity-Temperature-Depth instruments (CTD), the density which has strong ties to ocean dynamics and so on is computed according to equations of state for <span class="hlt">seawater</span>. This paper, based on density computational formulae in the Thermodynamic Equation of <span class="hlt">Seawater</span> 2010 (TEOS-10), follows the Guide of the expression of Uncertainty in Measurement (GUM) and assesses the main sources of uncertainties. By virtue of climatological decades-average temperature/Practical Salinity/pressure data sets in the global ocean provided by the National Oceanic and Atmospheric Administration (NOAA), correlation coefficients between uncertainty sources are determined and the combined standard uncertainties uc>(ρ>) in <span class="hlt">seawater</span> density calculations are evaluated. For grid points in the world ocean with 0.25° resolution, the standard deviations of uc>(ρ>) in vertical profiles cover the magnitude order of 10-4 kg m-3. The uc>(ρ>) means in vertical profiles of the Baltic Sea are about 0.028kg m-3 due to the larger scatter of Absolute Salinity anomaly. The distribution of the uc>(ρ>) means in vertical profiles of the world ocean except for the Baltic Sea, which covers the range of >(0.004,0.01>) kg m-3, is related to the correlation coefficient r>(SA,p>) between Absolute Salinity SA and pressure p. The results in the paper are based on sensors' measuring uncertainties of high accuracy CTD. Larger uncertainties in density calculations may arise if connected with lower sensors' specifications. This work may provide valuable uncertainty information required for reliability considerations of ocean circulation and global climate models.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013EGUGA..15.9940F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013EGUGA..15.9940F"><span>Initial evaluation of airborne water <span class="hlt">vapour</span> measurements by the IAGOS-GHG CRDS system</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Filges, Annette; Gerbig, Christoph; Smit, Herman G. J.; Krämer, Martina; Spelten, Nicole</p> <p>2013-04-01</p> <p>Accurate and reliable airborne measurements of water <span class="hlt">vapour</span> are still a challenge. Presently, no airborne humidity sensor exists that covers the entire range of water <span class="hlt">vapour</span> content between the surface and the upper troposphere/lower stratosphere (UT/LS) region with sufficient accuracy and time resolution. Nevertheless , these data are a pre-requisite to study the underlying processes in the chemistry and physics of the atmosphere. The DENCHAR project (Development and Evaluation of Novel Compact Hygrometer for Airborne Research) addresses this deficit by developing and characterizing novel or improved compact airborne hygrometers for different airborne applications within EUFAR (European Facility for Airborne Research). As part of the DENCHAR inter-comparison campaign in Hohn (Germany), 23 May - 1 June 2011, a commercial gas analyzer (G2401-m, Picarro Inc.,US), based on cavity ring-down spectroscopy (CRDS), was installed on a Learjet to measure water <span class="hlt">vapour</span>, CO2, CH4 and CO. The CRDS components are identical to those chosen for integration aboard commercial airliner within IAGOS (In-service Aircraft for a Global Observing System). Thus the campaign allowed for the initial assessment validation of the long-term IAGOS H2O measurements by CRDS against reference instruments with a long performance record (FISH, the Fast In-situ Stratospheric Hygrometer, and CR2 frostpoint hygrometer, both research centre Juelich). The inlet system, a one meter long 1/8" FEP-tube connected to a Rosemount TAT housing (model 102BX, deiced) installed on a window plate of the aircraft, was designed to eliminate sampling of larger aerosols, <span class="hlt">ice</span> particles, and water droplets, and provides about 90% of ram-pressure. In combination with a lowered sample flow of 0.1 slpm (corresponding to a 4 second response time), this ensured a fully controlled sample pressure in the cavity of 140 torr throughout an aircraft altitude operating range up to 12.5 km without the need of an upstream sampling pump</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23613802','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23613802"><span>Impediment to symbiosis establishment between giant clams and Symbiodinium algae due to sterilization of <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kurihara, Takeo; Yamada, Hideaki; Inoue, Ken; Iwai, Kenji; Hatta, Masayuki</p> <p>2013-01-01</p> <p>To survive the juvenile stage, giant clam juveniles need to establish a symbiotic relationship with the microalgae Symbiodinium occurring in the environment. The percentage of giant clam juveniles succeeding in symbiosis establishment ("symbiosis rate") is often low, which is problematic for seed producers. We investigated how and why symbiosis rates vary, depending on whether giant clam seeds are continuously reared in UV treated or non treated <span class="hlt">seawater</span>. Results repeatedly demonstrated that symbiosis rates were lower for UV treated <span class="hlt">seawater</span> than for non treated <span class="hlt">seawater</span>. Symbiosis rates were also lower for autoclaved <span class="hlt">seawater</span> and 0.2-µm filtered <span class="hlt">seawater</span> than for non treated <span class="hlt">seawater</span>. The decreased symbiosis rates in various sterilized <span class="hlt">seawater</span> suggest the possibility that some factors helping symbiosis establishment in natural <span class="hlt">seawater</span> are weakened owing to sterilization. The possible factors include vitality of giant clam seeds, since additional experiments revealed that survival rates of seeds reared alone without Symbiodinium were lower in sterilized <span class="hlt">seawater</span> than in non treated <span class="hlt">seawater</span>. In conclusion, UV treatment of <span class="hlt">seawater</span> was found to lead to decreased symbiosis rates, which is due possibly to some adverse effects common to the various sterilization techniques and relates to the vitality of the giant clam seeds.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29291835','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29291835"><span><span class="hlt">Ice</span> cream structure modification by <span class="hlt">ice</span>-binding proteins.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kaleda, Aleksei; Tsanev, Robert; Klesment, Tiina; Vilu, Raivo; Laos, Katrin</p> <p>2018-04-25</p> <p><span class="hlt">Ice</span>-binding proteins (IBPs), also known as antifreeze proteins, were added to <span class="hlt">ice</span> cream to investigate their effect on structure and texture. <span class="hlt">Ice</span> recrystallization inhibition was assessed in the <span class="hlt">ice</span> cream mixes using a novel accelerated microscope assay and the <span class="hlt">ice</span> cream microstructure was studied using an <span class="hlt">ice</span> crystal dispersion method. It was found that adding recombinantly produced fish type III IBPs at a concentration 3 mg·L -1 made <span class="hlt">ice</span> cream hard and crystalline with improved shape preservation during melting. <span class="hlt">Ice</span> creams made with IBPs (both from winter rye, and type III IBP) had aggregates of <span class="hlt">ice</span> crystals that entrapped pockets of the <span class="hlt">ice</span> cream mixture in a rigid network. Larger individual <span class="hlt">ice</span> crystals and no entrapment in control <span class="hlt">ice</span> creams was observed. Based on these results a model of <span class="hlt">ice</span> crystals aggregates formation in the presence of IBPs was proposed. Copyright © 2017 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4569698','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4569698"><span>Towards outperforming conventional sensor arrays with fabricated individual photonic <span class="hlt">vapour</span> sensors inspired by Morpho butterflies</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Potyrailo, Radislav A.; Bonam, Ravi K.; Hartley, John G.; Starkey, Timothy A.; Vukusic, Peter; Vasudev, Milana; Bunning, Timothy; Naik, Rajesh R.; Tang, Zhexiong; Palacios, Manuel A.; Larsen, Michael; Le Tarte, Laurie A.; Grande, James C.; Zhong, Sheng; Deng, Tao</p> <p>2015-01-01</p> <p>Combining <span class="hlt">vapour</span> sensors into arrays is an accepted compromise to mitigate poor selectivity of conventional sensors. Here we show individual nanofabricated sensors that not only selectively detect separate <span class="hlt">vapours</span> in pristine conditions but also quantify these <span class="hlt">vapours</span> in mixtures, and when blended with a variable moisture background. Our sensor design is inspired by the iridescent nanostructure and gradient surface chemistry of Morpho butterflies and involves physical and chemical design criteria. The physical design involves optical interference and diffraction on the fabricated periodic nanostructures and uses optical loss in the nanostructure to enhance the spectral diversity of reflectance. The chemical design uses spatially controlled nanostructure functionalization. Thus, while quantitation of analytes in the presence of variable backgrounds is challenging for most sensor arrays, we achieve this goal using individual multivariable sensors. These colorimetric sensors can be tuned for numerous <span class="hlt">vapour</span> sensing scenarios in confined areas or as individual nodes for distributed monitoring. PMID:26324320</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70011998','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70011998"><span><span class="hlt">Seawater</span> sulfate reduction and sulfur isotope fractionation in basaltic systems: interaction of <span class="hlt">seawater</span> with fayalite and magnetite at 200–350°C</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Shanks, Wayne C.; Bischoff, James L.; Rosenbauer, Robert J.</p> <p>1981-01-01</p> <p>Systematics of sulfur isotopes in the 250 and 350°C experiments indicate that isotopic equilibrium is reached, and can be modeled as a Rayleigh distillation process. Isotopic composition of hydrothermally produced H2S in natural systems is strongly dependent upon the <span class="hlt">seawater</span>/basalt ratio in the geothermal system, which controls the relative sulfide contributions from the two important sulfur sources, <span class="hlt">seawater</span> sulfate and sulfide phases in basalt. Anhydrite precipitation during geothermal heating severely limits sulfate ingress into high temperature interaction zones. Quantitative sulfate reduction can thus be accomplished without producing strongly oxidized rocks and resultant sulfide sulfur isotope values represent a mixture of <span class="hlt">seawater</span> and basaltic sulfur.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27206961','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27206961"><span>Experimental provocation of '<span class="hlt">ice</span>-cream headache' by <span class="hlt">ice</span> cubes and <span class="hlt">ice</span> water.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mages, Stephan; Hensel, Ole; Zierz, Antonia Maria; Kraya, Torsten; Zierz, Stephan</p> <p>2017-04-01</p> <p>Background There are various studies on experimentally provoked '<span class="hlt">ice</span>-cream headache' or 'headache attributed to ingestion or inhalation of a cold stimulus' (HICS) using different provocation protocols. The aim of this study was to compare two provocation protocols. Methods <span class="hlt">Ice</span> cubes pressed to the palate and fast ingestion of <span class="hlt">ice</span> water were used to provoke HICS and clinical features were compared. Results The <span class="hlt">ice</span>-water stimulus provoked HICS significantly more often than the <span class="hlt">ice</span>-cube stimulus (9/77 vs. 39/77). <span class="hlt">Ice</span>-water-provoked HICS had a significantly shorter latency (median 15 s, range 4-97 s vs. median 68 s, range 27-96 s). There was no difference in pain localisation. Character after <span class="hlt">ice</span>-cube stimulation was predominantly described as pressing and after <span class="hlt">ice</span>-water stimulation as stabbing. A second HICS followed in 10/39 (26%) of the headaches provoked by <span class="hlt">ice</span> water. Lacrimation occurred significantly more often in volunteers with than in those without HICS. Discussion HICS provoked by <span class="hlt">ice</span> water was more frequent, had a shorter latency, different pain character and higher pain intensity than HICS provoked by <span class="hlt">ice</span> cubes. The finding of two subsequent HICS attacks in the same volunteers supports the notion that two types of HICS exist. Lacrimation during HICS indicates involvement of the trigeminal-autonomic reflex.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016DPS....4851308S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016DPS....4851308S"><span>Periglacial complexes in Utopia Planitia: rimless, tiered depressions, (clastically) sorted and unsorted polygonised terrain and an <span class="hlt">ice</span>-rich mantle</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Soare, Richard; Conway, Susan; Gallagher, Colman; Dohm, James; Clifford, Stephen M.; Williams, Jean-pierre</p> <p>2016-10-01</p> <p>We report the spatial and possible genetic-relationship at the mid-latitudes of Utopia Planitia (45-500N 115-1200E), Mars, of: (a) metre to decametre deep, rimless, tiered depressions; terrain that exhibits (b) (clastically) sorted and (c) unsorted (small-sized) polygons; and, (d) a very youthful, <span class="hlt">ice</span>-rich mantle. We show that these individual landscape features are separated stratigraphically, this being presented to the Mars community for the first time, and suggest that the stratigraphical separation of these features could be the result of boundary conditions and formation processes that have varied much more widely than has been thought hitherto. In cold-climate and non-glacial regions such as the Yamal Peninsula of eastern Russia and the Tuktoyaktuk Coastlands of northern Canada, landscape assemblages comprised of similar features are referenced as "<span class="hlt">ice</span> complexes" and are indicative of periglacialism on two fronts: first, the presence of "<span class="hlt">ice</span>-rich" permafrost or permafrost comprised of "excess <span class="hlt">ice</span>", i.e. "permafrost" whose pore space is exceeded by the "water <span class="hlt">ice</span>" within that body of sediment; and, second, antecedently or currently active freeze-thaw cycling, minimally, to the full depth of the "<span class="hlt">ice</span>-complex" depressions. In the Dry Valleys of the Antarctic, where the atmospheric aridity and cold-temperatures approach those of Mars, <span class="hlt">ice-vapour</span> diffusion and adsorption cycles are cited as the means by which the near-surface, permafrost, i.e. ≤1m deep, has become <span class="hlt">ice</span>-cemented. However, the metre to decametre depths of the "<span class="hlt">ice</span>-complex" depressions on Earth and the morphologically-similar ones on Mars lie beyond the vertical reach of the Antarctic diffusion and adsorption cycles, both empirically and theoretically. By deduction, this points to the freeze-thaw cycling of water to depth, fostered either by exogenic or endogenic means, perhaps playing a more important role in the formation of the possible Martian "<span class="hlt">ice</span> complexes" than might be expected were</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=distillation&pg=6&id=EJ344406','ERIC'); return false;" href="https://eric.ed.gov/?q=distillation&pg=6&id=EJ344406"><span>Distillation with <span class="hlt">Vapour</span> Compression. An Undergraduate Experimental Facility.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Pritchard, Colin</p> <p>1986-01-01</p> <p>Discusses the need to design distillation columns that are more energy efficient. Describes a "design and build" project completed by two college students aimed at demonstrating the principles of <span class="hlt">vapour</span> compression distillation in a more energy efficient way. General design specifications are given, along with suggestions for teaching…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009EGUGA..11.9152A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009EGUGA..11.9152A"><span>The Particle Habit Imaging and Polar Scattering probe PHIPS: First Stereo-Imaging and Polar Scattering Function Measurements of <span class="hlt">Ice</span> Particles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Abdelmonem, A.; Schnaiter, M.; Schön, R.; Leisner, T.</p> <p>2009-04-01</p> <p>Cirrus clouds impact climate by their influence on the water <span class="hlt">vapour</span> distribution in the upper troposphere. Moreover, they directly affect the radiative balance of the Earth's atmosphere by the scattering of incoming solar radiation and the absorption of outgoing thermal emission. The link between the microphysical properties of <span class="hlt">ice</span> cloud particles and the radiative forcing of the clouds is not as yet well understood and the influence of the shapes of <span class="hlt">ice</span> crystals on the radiative budget of cirrus clouds is currently under debate. PHIPS is a new experimental device for the stereo-imaging of individual cloud particles and the simultaneous measurement of the polar scattering function of the same particle. PHIPS uses an automated particle event triggering system that ensures that only those particles are captured which are located in the field of view - depth of field volume of the microscope unit. Efforts were made to improve the resolution power of the microscope unit down to about 3 µm and to facilitate a 3D morphology impression of the <span class="hlt">ice</span> crystals. This is realised by a stereo-imaging set up composed of two identical microscopes which image the same particle under an angular viewing distance of 30°. The scattering part of PHIPS enables the measurement of the polar light scattering function of cloud particles with an angular resolution of 1° for forward scattering directions (from 1° to 10°) and 8° for side and backscattering directions (from 18° to 170°). For each particle the light scattering pulse per channel is stored either as integrated intensity or as time resolved intensity function which opens a new category of data analysis concerning details of the particle movement. PHIPS is the first step to PHIPS-HALO which is one of the in situ <span class="hlt">ice</span> particle and water <span class="hlt">vapour</span> instruments that are currently under development for the new German research aircraft HALO. The instrument was tested in the <span class="hlt">ice</span> cloud characterisation campaign HALO-02 which was conducted</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015JPlPh..81e4902B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015JPlPh..81e4902B"><span>Complex astrophysical experiments relating to jets, solar loops, and water <span class="hlt">ice</span> dusty plasma</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bellan, P. M.; Zhai, X.; Chai, K. B.; Ha, B. N.</p> <p>2015-10-01</p> <p>> Recent results of three astrophysically relevant experiments at Caltech are summarized. In the first experiment magnetohydrodynamically driven plasma jets simulate astrophysical jets that undergo a kink instability. Lateral acceleration of the kinking jet spawns a Rayleigh-Taylor instability, which in turn spawns a magnetic reconnection. Particle heating and a burst of waves are observed in association with the reconnection. The second experiment uses a slightly different setup to produce an expanding arched plasma loop which is similar to a solar corona loop. It is shown that the plasma in this loop results from jets originating from the electrodes. The possibility of a transition from slow to fast expansion as a result of the expanding loop breaking free of an externally imposed strapping magnetic field is investigated. The third and completely different experiment creates a weakly ionized plasma with liquid nitrogen cooled electrodes. Water <span class="hlt">vapour</span> injected into this plasma forms water <span class="hlt">ice</span> grains that in general are ellipsoidal and not spheroidal. The water <span class="hlt">ice</span> grains can become quite long (up to several hundred microns) and self-organize so that they are evenly spaced and vertically aligned.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA531082','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA531082"><span>Simultaneous Extraction of Lithium and Hydrogen From <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2010-10-26</p> <p>etc.) References 1. U. Bardi , Extracting minerals from <span class="hlt">seawater</span>: An energy analysis, Sustainability, 2, 980 (2010). 2. K-S. Chung, J -C. Lee, W...Michele Anderson, ONR Code: 332, michele.anderson1@navy.mil Project Objective: The ultimate goal of the proposed research is to demonstrate a ...novel electrolytic process for extracting Li from <span class="hlt">seawater</span>, which contains a number of valuable metals (Table1). 1 The technical objectives of this</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/17937301','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/17937301"><span>Modeling the effect of snow and <span class="hlt">ice</span> on the global environmental fate and long-range transport potential of semivolatile organic compounds.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stocker, Judith; Scheringer, Martin; Wegmann, Fabio; Hungerbuhler, Konrad</p> <p>2007-09-01</p> <p>Snow and <span class="hlt">ice</span> have been implemented in a global multimedia box model to investigate the influence of these media on the environmental fate and long-range transport (LRT) of semivolatile organic compounds (SOCs). Investigated compounds include HCB, PCB28, PCB180, PBDE47, PBDE209, alpha-HCH, and dacthal. In low latitudes, snow acts as a transfer medium taking up chemicals from air and releasing them to water or soil during snowmelt. In high latitudes, snow and <span class="hlt">ice</span> shield water, soil, and vegetation from chemical deposition. In the model version including snow and <span class="hlt">ice</span> (scenario 2), the mass of chemicals in soil in high latitudes is between 27% (HCB) and 97% (alpha-HCH) of the mass calculated with the model version without snow and <span class="hlt">ice</span> (scenario 1). Amounts in Arctic <span class="hlt">seawater</span> in scenario 2 are 8% (alpha-HCH) to 21% (dacthal) of the amounts obtained in scenario 1. For all investigated chemicals except alpha-HCH, presence of snow and <span class="hlt">ice</span> in the model increases the concentration in air by a factor of 2 (HCB)to 10 (PBDE209). Because of reduced net deposition to snow-covered surfaces in high latitudes, LRT to the Arctic is reduced for most chemicals whereas transport to the south is more pronounced than in scenario 1 ("southward shift"). The presence of snow and <span class="hlt">ice</span> thus considerably changes the environmental fate of SOCs.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_14");'>14</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li class="active"><span>16</span></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_16 --> <div id="page_17" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="321"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3628887','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3628887"><span>Impediment to Symbiosis Establishment between Giant Clams and Symbiodinium Algae Due to Sterilization of <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Kurihara, Takeo; Yamada, Hideaki; Inoue, Ken; Iwai, Kenji; Hatta, Masayuki</p> <p>2013-01-01</p> <p>To survive the juvenile stage, giant clam juveniles need to establish a symbiotic relationship with the microalgae Symbiodinium occurring in the environment. The percentage of giant clam juveniles succeeding in symbiosis establishment (“symbiosis rate”) is often low, which is problematic for seed producers. We investigated how and why symbiosis rates vary, depending on whether giant clam seeds are continuously reared in UV treated or non treated <span class="hlt">seawater</span>. Results repeatedly demonstrated that symbiosis rates were lower for UV treated <span class="hlt">seawater</span> than for non treated <span class="hlt">seawater</span>. Symbiosis rates were also lower for autoclaved <span class="hlt">seawater</span> and 0.2-µm filtered <span class="hlt">seawater</span> than for non treated <span class="hlt">seawater</span>. The decreased symbiosis rates in various sterilized <span class="hlt">seawater</span> suggest the possibility that some factors helping symbiosis establishment in natural <span class="hlt">seawater</span> are weakened owing to sterilization. The possible factors include vitality of giant clam seeds, since additional experiments revealed that survival rates of seeds reared alone without Symbiodinium were lower in sterilized <span class="hlt">seawater</span> than in non treated <span class="hlt">seawater</span>. In conclusion, UV treatment of <span class="hlt">seawater</span> was found to lead to decreased symbiosis rates, which is due possibly to some adverse effects common to the various sterilization techniques and relates to the vitality of the giant clam seeds. PMID:23613802</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018OcSci..14...15S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018OcSci..14...15S"><span>The density-salinity relation of standard <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Schmidt, Hannes; Seitz, Steffen; Hassel, Egon; Wolf, Henning</p> <p>2018-01-01</p> <p>The determination of salinity by means of electrical conductivity relies on stable salt proportions in the North Atlantic Ocean, because standard <span class="hlt">seawater</span>, which is required for salinometer calibration, is produced from water of the North Atlantic. To verify the long-term stability of the standard <span class="hlt">seawater</span> composition, it was proposed to perform measurements of the standard <span class="hlt">seawater</span> density. Since the density is sensitive to all salt components, a density measurement can detect any change in the composition. A conversion of the density values to salinity can be performed by means of a density-salinity relation. To use such a relation with a target uncertainty in salinity comparable to that in salinity obtained from conductivity measurements, a density measurement with an uncertainty of 2 g m-3 is mandatory. We present a new density-salinity relation based on such accurate density measurements. The substitution measurement method used is described and density corrections for uniform isotopic and chemical compositions are reported. The comparison of densities calculated using the new relation with those calculated using the present reference equations of state TEOS-10 suggests that the density accuracy of TEOS-10 (as well as that of EOS-80) has been overestimated, as the accuracy of some of its underlying density measurements had been overestimated. The new density-salinity relation may be used to verify the stable composition of standard <span class="hlt">seawater</span> by means of routine density measurements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=STS048-152-007&hterms=5S&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D80%26Ntt%3D5S','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=STS048-152-007&hterms=5S&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D80%26Ntt%3D5S"><span>Breakup of Pack <span class="hlt">Ice</span>, Antarctic <span class="hlt">Ice</span> Shelf</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p></p> <p>1991-01-01</p> <p>Breakup of Pack <span class="hlt">Ice</span> along the periphery of the Antarctic <span class="hlt">Ice</span> Shelf (53.5S, 3.0E) produced this mosaic of <span class="hlt">ice</span> floes off the Antarctic <span class="hlt">Ice</span> Shelf. Strong offshore winds, probably associated with strong katabatic downdrafts from the interior of the continent, are seen peeling off the edges of the <span class="hlt">ice</span> shelf into long filamets of sea <span class="hlt">ice</span>, icebergs, bergy bits and growlers to flow northward into the South Atlantic Ocean. 53.5S, 3.0E</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23182665','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23182665"><span>Petroleum hydrocarbon contaminations in the intertidal <span class="hlt">seawater</span> after the Hebei Spirit oil spill--effect of tidal cycle on the TPH concentrations and the chromatographic characterization of <span class="hlt">seawater</span> extracts.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kim, Moonkoo; Hong, Sang Hee; Won, Jongho; Yim, Un Hyuk; Jung, Jee-Hyun; Ha, Sung Yong; An, Joon Geon; Joo, Changkyu; Kim, Eunsic; Han, Gi Myung; Baek, Seongho; Choi, Hyun-Woo; Shim, Won Joon</p> <p>2013-02-01</p> <p>In December 2007, the oil tanker Hebei Spirit released approximately 12,547,000 L of crude oil off the west coast of Korea, impacting more than 375 km of coastline. The <span class="hlt">seawater</span> TPH concentrations immediately after the spill ranged from 1.5 to 7310 μg L⁻¹, with an average of 732 μg L⁻¹. The concentrations appeared to decrease drastically to 2.0-224 μg L⁻¹ in one month after the spill. The TPH concentrations in <span class="hlt">seawater</span> fluctuated with time thereafter because of the remobilization of oil by continuing shoreline cleanup activities and subsequent wave/tidal actions. <span class="hlt">Seawater</span> TPH concentrations were much higher during high tide than during low tide due to the resuspension of stranded oil. The variation of TPH levels in <span class="hlt">seawater</span> also matched the spring-neap tidal cycle in the study areas for the first three weeks of the study. Comparisons of the gas chromatograms of the <span class="hlt">seawater</span> with the water accommodated fraction and the cargo oil indicated that <span class="hlt">seawater</span> samples were contaminated mainly by the dispersed droplets of spilled oil. One year of monitoring revealed that the oil content in <span class="hlt">seawater</span> had clearly decreased at most sites, although some regional fluctuations of oil contamination were noted until June 2008. Copyright © 2012 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3105315','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3105315"><span>High efficiency coherent optical memory with warm rubidium <span class="hlt">vapour</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Hosseini, M.; Sparkes, B.M.; Campbell, G.; Lam, P.K.; Buchler, B.C.</p> <p>2011-01-01</p> <p>By harnessing aspects of quantum mechanics, communication and information processing could be radically transformed. Promising forms of quantum information technology include optical quantum cryptographic systems and computing using photons for quantum logic operations. As with current information processing systems, some form of memory will be required. Quantum repeaters, which are required for long distance quantum key distribution, require quantum optical memory as do deterministic logic gates for optical quantum computing. Here, we present results from a coherent optical memory based on warm rubidium <span class="hlt">vapour</span> and show 87% efficient recall of light pulses, the highest efficiency measured to date for any coherent optical memory suitable for quantum information applications. We also show storage and recall of up to 20 pulses from our system. These results show that simple warm atomic <span class="hlt">vapour</span> systems have clear potential as a platform for quantum memory. PMID:21285952</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/21285952','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/21285952"><span>High efficiency coherent optical memory with warm rubidium <span class="hlt">vapour</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hosseini, M; Sparkes, B M; Campbell, G; Lam, P K; Buchler, B C</p> <p>2011-02-01</p> <p>By harnessing aspects of quantum mechanics, communication and information processing could be radically transformed. Promising forms of quantum information technology include optical quantum cryptographic systems and computing using photons for quantum logic operations. As with current information processing systems, some form of memory will be required. Quantum repeaters, which are required for long distance quantum key distribution, require quantum optical memory as do deterministic logic gates for optical quantum computing. Here, we present results from a coherent optical memory based on warm rubidium <span class="hlt">vapour</span> and show 87% efficient recall of light pulses, the highest efficiency measured to date for any coherent optical memory suitable for quantum information applications. We also show storage and recall of up to 20 pulses from our system. These results show that simple warm atomic <span class="hlt">vapour</span> systems have clear potential as a platform for quantum memory.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017E%26ES...52a2067Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017E%26ES...52a2067Z"><span>The salinity gradient power generating system integrated into the <span class="hlt">seawater</span> desalination system</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhu, Yongqiang; Wang, Wanjun; Cai, Bingqian; Hao, Jiacheng; Xia, Ruihua</p> <p>2017-01-01</p> <p><span class="hlt">Seawater</span> desalination is an important way to solve the problem of fresh water shortage. Low energy efficiency and high cost are disadvantages existing in <span class="hlt">seawater</span> desalination. With huge reserve and the highest energy density among different types of marine energy, salinity gradient energy has a bright application prospect. The promotion of traditional salinity gradient power generating systems is hindered by its low efficiency and specific requirements on site selection. This paper proposes a salinity gradient power generating system integrated into the <span class="hlt">seawater</span> desalination system which combines the salinity gradient power generating system and the <span class="hlt">seawater</span> desalination system aiming to remedy the aforementioned deficiency and could serve as references for future <span class="hlt">seawater</span> desalination and salinity gradient energy exploitation. The paper elaborates on the operating principles of the system, analyzes the detailed working process, and estimates the energy output and consumption of the system. It is proved that with appropriate design, the energy output of the salinity gradient power generating system can satisfy the demand of the <span class="hlt">seawater</span> desalination system.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26775725','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26775725"><span>Trematomus bernacchii as an indicator of POP temporal trend in the Antarctic <span class="hlt">seawaters</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cincinelli, Alessandra; Martellini, Tania; Pozo, Karla; Kukučka, Petr; Audy, Ondřej; Corsolini, Simonetta</p> <p>2016-10-01</p> <p>The occurrence of POPs in remote areas, such as Antarctica, is the result of their ability to udergo Long Range Transport (LRT) in the atmosphere, precipitation and cold condensation. In this study, both recent levels of various POPs in Trematomus bernacchii and their changes in roughly three decades were determined in order to evaluate trends of POPs in Antarctic benthic <span class="hlt">seawaters</span>. In fact, Trematomus bernacchii is considered a good sentinel bio-indicator for monitoring not only the extent of contamination by POPs in the Antarctic aquatic ecosystem, but also changes in Antarctic ecosystem quality and trends. A slight decreasing PCB trend was detected during 30-years time span (from early 1980's to 2010) in the circumantarctic <span class="hlt">seawaters</span>. Two higher peaks of concentrations were reported in 2001 and 2005 in the Ross Sea and they may reflect the <span class="hlt">ice</span> melting of icebergs. Because fire risk is very high in Antarctica due to the very dry air, a large use of flame retardants in buildings and furniture of stations is highly probable; moreover, many stations were built when there were no restrictions on flame retardants use. The PBDE levels in the T. bernacchii from 2001 to 2011 ranged 0.05-0.35 pg/g and were of the same order of magnitude in 2001/2011 and in 2002/2005, with a maximum value in 2005 (0.35 pg/g). Comparable concentrations of HCB, HCHs PCDDs and PCDFs are available only for few seasons: all these compounds showed a decreasing temporal trends and their concentrations were one or more order of magnitude lower in 2000s-2010s. Copyright © 2015 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.A51D2093K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.A51D2093K"><span>Dynamic Bubble Surface Tension Measurements in Northwest Atlantic <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Kieber, D. J.; Long, M. S.; Keene, W. C.; Kinsey, J. D.; Frossard, A. A.; Beaupre, S. R.; Duplessis, P.; Maben, J. R.; Lu, X.; Chang, R.; Zhu, Y.; Bisgrove, J.</p> <p>2017-12-01</p> <p>Numerous reports suggest that most organic matter (OM) associated with newly formed primary marine aerosol (PMA) originates from the sea-surface microlayer. However, surface-active OM rapidly adsorbs onto bubble surfaces in the water column and is ejected into the atmosphere when bubbles burst at the air-water interface. Here we present dynamic surface tension measurements of bubbles produced in near surface <span class="hlt">seawater</span> from biologically productive and oligotrophic sites and in deep <span class="hlt">seawater</span> collected from 2500 m in the northwest Atlantic. In all cases, the surface tension of bubble surfaces decreased within seconds after the bubbles were exposed to <span class="hlt">seawater</span>. These observations demonstrate that bubble surfaces are rapidly saturated by surfactant material scavenged from <span class="hlt">seawater</span>. Spatial and diel variability in bubble surface evolution indicate corresponding variability in surfactant concentrations and/or composition. Our results reveal that surface-active OM is found throughout the water column, and that at least some surfactants are not of recent biological origin. Our results also support the hypothesis that the surface microlayer is a minor to negligible source of OM associated with freshly produced PMA.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..1817750K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..1817750K"><span>ESA's <span class="hlt">Ice</span> Cloud Imager on Metop Second Generation</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Klein, Ulf; Loiselet, Marc; Mason, Graeme; Gonzalez, Raquel; Brandt, Michael</p> <p>2016-04-01</p> <p>Since 2006, the European contribution to operational meteorological observations from polar orbit has been provided by the Meteorological Operational (MetOp) satellites, which is the space segment of the EUMETSAT Polar System (EPS). The first MetOp satellite was launched in 2006, 2nd 2012 and 3rd satellite is planned for launch in 2018. As part of the next generation EUMETSAT Polar System (EPS-SG), the MetOp Second Generation (MetOp-SG) satellites will provide continuity and enhancement of these observations in the 2021 - 2042 timeframe. The noel <span class="hlt">Ice</span> Cloud Imager (ICI) is one of the instruments selected to be on-board the MetOp-SG satellite "B". The main objective of the ICI is to enable cloud <span class="hlt">ice</span> retrieval, with emphasis on cirrus clouds. ICI will provide information on cloud <span class="hlt">ice</span> mean altitude, cloud <span class="hlt">ice</span> water path and cloud <span class="hlt">ice</span> effective radius. In addition, it will provide water <span class="hlt">vapour</span> profile measurement capability. ICI is a 13-channel microwave/sub-millimetre wave radiometer, covering the frequency range from 183 GHz up to 664 GHz. The instrument is composed of a rotating part and a fixed part. The rotating part includes the main antenna, the feed assembly and the receiver electronics. The fixed part contains the hot calibration target, the reflector for viewing the cold sky and the electronics for the instrument control and interface with the platform. Between the fixed and the rotating part is the scan mechanism. Scan mechanism is not only responsible of rotating the instrument and providing its angular position, but it will also have pass through the power and data lines. The Scan mechanism is controlled by the fully redundant Control and Drive Electronics ICI is calibrated using an internal hot target and a cold sky mirror, which are viewed once per rotation. The internal hot target is a traditional pyramidal target. The hot target is covered by an annular shield during rotation with only a small opening for the feed horns to guarantee a stable environment</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27025155','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27025155"><span><span class="hlt">Ice</span>-shell purification of <span class="hlt">ice</span>-binding proteins.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Marshall, Craig J; Basu, Koli; Davies, Peter L</p> <p>2016-06-01</p> <p><span class="hlt">Ice</span>-affinity purification is a simple and efficient method of purifying to homogeneity both natural and recombinant <span class="hlt">ice</span>-binding proteins. The purification involves the incorporation of <span class="hlt">ice</span>-binding proteins into slowly-growing <span class="hlt">ice</span> and the exclusion of other proteins and solutes. In previous approaches, the <span class="hlt">ice</span> was grown around a hollow brass finger through which coolant was circulated. We describe here an easily-constructed apparatus that employs <span class="hlt">ice</span> affinity purification that not only shortens the time for purification from 1-2 days to 1-2 h, but also enhances yield and purity. In this apparatus, the surface area for the separation was increased by extracting the <span class="hlt">ice</span>-binding proteins into an <span class="hlt">ice</span>-shell formed inside a rotating round-bottom flask partially submerged in a sub-zero bath. In principle, any <span class="hlt">ice</span>-binding compound can be recovered from liquid solution, and the method is readily scalable. Copyright © 2016 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20030068097','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20030068097"><span>Quantification of <span class="hlt">Ice</span> Accretions for <span class="hlt">Icing</span> Scaling Evaluations</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Ruff, Gary A.; Anderson, David N.</p> <p>2003-01-01</p> <p>The comparison of <span class="hlt">ice</span> accretion characteristics is an integral part of aircraft <span class="hlt">icing</span> research. It is often necessary to compare an <span class="hlt">ice</span> accretion obtained from a flight test or numerical simulation to one produced in an <span class="hlt">icing</span> wind tunnel or for validation of an <span class="hlt">icing</span> scaling method. Traditionally, this has been accomplished by overlaying two-dimensional tracings of <span class="hlt">ice</span> accretion shapes. This paper addresses the basic question of how to compare <span class="hlt">ice</span> accretions using more quantitative methods. For simplicity, geometric characteristics of the <span class="hlt">ice</span> accretions are used for the comparison. One method evaluated is a direct comparison of the percent differences of the geometric measurements. The second method inputs these measurements into a fuzzy inference system to obtain a single measure of the goodness of the comparison. The procedures are demonstrated by comparing <span class="hlt">ice</span> shapes obtained in the <span class="hlt">Icing</span> Research Tunnel at NASA Glenn Research Center during recent <span class="hlt">icing</span> scaling tests. The results demonstrate that this type of analysis is useful in quantifying the similarity of <span class="hlt">ice</span> accretion shapes and that the procedures should be further developed by expanding the analysis to additional <span class="hlt">icing</span> data sets.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1391653-amicrowave-satellite-water-vapour-column-retrieval-polar-winter-conditions','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1391653-amicrowave-satellite-water-vapour-column-retrieval-polar-winter-conditions"><span>A microwave satellite water <span class="hlt">vapour</span> column retrieval for polar winter conditions</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Perro, Christopher; Lesins, Glen; Duck, Thomas J.</p> <p></p> <p>A new microwave satellite water <span class="hlt">vapour</span> retrieval for the polar winter atmosphere is presented. The retrieval builds on the work of Miao et al. (2001) and Melsheimer and Heygster (2008), employing auxiliary information for atmospheric conditions and numerical optimization. It was tested using simulated and actual measurements from the Microwave Humidity Sounder (MHS) satellite instruments. Ground truth was provided by the G-band <span class="hlt">vapour</span> radiometer (GVR) at Barrow, Alaska. For water <span class="hlt">vapour</span> columns less than 6 kg m -2, comparisons between the retrieval and GVR result in a root mean square (RMS) deviation of 0.39 kg m -2 and a systematic bias of 0.08 kg m -2. These results aremore » compared with RMS deviations and biases at Barrow for the retrieval of Melsheimer and Heygster (2008), the AIRS and MIRS satellite data products, and the ERA-Interim, NCEP, JRA-55, and ASR reanalyses. When applied to MHS measurements, the new retrieval produces a smaller RMS deviation and bias than for the earlier retrieval and satellite data products. The RMS deviations for the new retrieval were comparable to those for the ERA-Interim, JRA-55, and ASR reanalyses; however, the MHS retrievals have much finer horizontal resolution (15 km at nadir) and reveal more structure. The new retrieval can be used to obtain pan-Arctic maps of water <span class="hlt">vapour</span> columns of unprecedented quality. It may also be applied to measurements from the Special Sensor Microwave/Temperature 2 (SSM/T2), Advanced Microwave Sounding Unit B (AMSU-B), Special Sensor Microwave Imager/Sounder (SSMIS), Advanced Technology Microwave Sounder (ATMS), and Chinese MicroWave Humidity Sounder (MWHS) instruments.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20000044552','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20000044552"><span><span class="hlt">Ice</span> Accretions and <span class="hlt">Icing</span> Effects for Modern Airfoils</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Addy, Harold E., Jr.</p> <p>2000-01-01</p> <p><span class="hlt">Icing</span> tests were conducted to document <span class="hlt">ice</span> shapes formed on three different two-dimensional airfoils and to study the effects of the accreted <span class="hlt">ice</span> on aerodynamic performance. The models tested were representative of airfoil designs in current use for each of the commercial transport, business jet, and general aviation categories of aircraft. The models were subjected to a range of <span class="hlt">icing</span> conditions in an <span class="hlt">icing</span> wind tunnel. The conditions were selected primarily from the Federal Aviation Administration's Federal Aviation Regulations 25 Appendix C atmospheric <span class="hlt">icing</span> conditions. A few large droplet <span class="hlt">icing</span> conditions were included. To verify the aerodynamic performance measurements, molds were made of selected <span class="hlt">ice</span> shapes formed in the <span class="hlt">icing</span> tunnel. Castings of the <span class="hlt">ice</span> were made from the molds and placed on a model in a dry, low-turbulence wind tunnel where precision aerodynamic performance measurements were made. Documentation of all the <span class="hlt">ice</span> shapes and the aerodynamic performance measurements made during the <span class="hlt">icing</span> tunnel tests is included in this report. Results from the dry, low-turbulence wind tunnel tests are also presented.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA601068','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA601068"><span>Sunlight, Sea <span class="hlt">Ice</span>, and the <span class="hlt">Ice</span> Albedo Feedback in a Changing Arctic Sea <span class="hlt">Ice</span> Cover</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2013-09-30</p> <p>Sea <span class="hlt">Ice</span> , and the <span class="hlt">Ice</span> Albedo Feedback in a...COVERED 00-00-2013 to 00-00-2013 4. TITLE AND SUBTITLE Sunlight, Sea <span class="hlt">Ice</span> , and the <span class="hlt">Ice</span> Albedo Feedback in a Changing Arctic Sea <span class="hlt">Ice</span> Cover 5a...during a period when incident solar irradiance is large increasing solar heat input to the <span class="hlt">ice</span> . Seasonal sea <span class="hlt">ice</span> typically has a smaller albedo</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20851909','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20851909"><span>Zhongshania antarctica gen. nov., sp. nov. and Zhongshania guokunii sp. nov., gammaproteobacteria respectively isolated from coastal attached (fast) <span class="hlt">ice</span> and surface <span class="hlt">seawater</span> of the Antarctic.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Li, Hui-Juan; Zhang, Xi-Ying; Chen, Chun-Xiao; Zhang, Yan-Jiao; Gao, Zhao-Ming; Yu, Yong; Chen, Xiu-Lan; Chen, Bo; Zhang, Yu-Zhong</p> <p>2011-09-01</p> <p>Two Gram-negative, motile, aerobic, catalase- and oxidase-positive, rod-shaped strains, designated ZS5-23(T) and ZS6-22(T), were respectively isolated from Antarctic coastal attached (fast) <span class="hlt">ice</span> and surface <span class="hlt">seawater</span> samples. Both strains could grow at 4-35 °C (optimum 30 °C) and in the absence of NaCl. Analyses of 16S rRNA gene sequences revealed that strains ZS5-23(T) and ZS6-22(T) were closely related to each other (99.0 % sequence similarity) and belonged to the class Gammaproteobacteria, with their closest relatives being Spongiibacter and Melitea species (93.1-94.3 % sequence similarity). The predominant cellular fatty acids in both strains were C₁₇:₁ω8c, C₁₇:₀ and summed feature 3 (C₁₆:₁ω7c and/or iso-C₁₅:₀ 2-OH). Genomic DNA G+C contents of strains ZS5-23(T) and ZS6-22(T) were 51.5 and 51.8 mol%, respectively. The DNA-DNA relatedness between strains ZS5-23(T) and ZS6-22(T) was 50.9 %. Strains ZS5-23(T) and ZS6-22(T) could be differentiated from each other and from Spongiibacter and Melitea species by differences in a number of phenotypic properties. Based on the data presented, strains ZS5-23(T) and ZS6-22(T) represent two novel species in a new genus in the class Gammaproteobacteria, for which the names Zhongshania antarctica gen. nov., sp. nov. (the type species) and Zhongshania guokunii sp. nov. are proposed. The type strain of Zhongshania antarctica is ZS5-23(T) ( = KACC 14066(T)  = CCTCC AB 209246(T)) and that of Zhongshania guokunii is ZS6-22(T) ( = KACC 14532(T)  = CCTCC AB 209247(T)).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24849267','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24849267"><span>Leidenfrost <span class="hlt">vapour</span> layer moderation of the drag crisis and trajectories of superhydrophobic and hydrophilic spheres falling in water.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Vakarelski, Ivan U; Chan, Derek Y C; Thoroddsen, Sigurdur T</p> <p>2014-08-21</p> <p>We investigate the dynamic effects of a Leidenfrost <span class="hlt">vapour</span> layer sustained on the surface of heated steel spheres during free fall in water. We find that a stable <span class="hlt">vapour</span> layer sustained on the textured superhydrophobic surface of spheres falling through 95 °C water can reduce the hydrodynamic drag by up to 75% and stabilize the sphere trajectory for the Reynolds number between 10(4) and 10(6), spanning the drag crisis in the absence of the <span class="hlt">vapour</span> layer. For hydrophilic spheres under the same conditions, the transition to drag reduction and trajectory stability occurs abruptly at a temperature different from the static Leidenfrost point. The observed drag reduction effects are attributed to the disruption of the viscous boundary layer by the <span class="hlt">vapour</span> layer whose thickness depends on the water temperature. Both the drag reduction and the trajectory stabilization effects are expected to have significant implications for development of sustainable <span class="hlt">vapour</span> layer based technologies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C21H..03W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C21H..03W"><span>The colors of icebergs</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Warren, S. G.</p> <p>2017-12-01</p> <p>Ordinary icebergs of meteoric glacier <span class="hlt">ice</span> appear bluish-white, i.e. intermediate in color between the white of snow and the blue of pure <span class="hlt">ice</span>, depending on the bubble content. However, clear dark bubble-free icebergs are occasionally seen in the Antarctic Ocean; they originate from freezing of <span class="hlt">seawater</span> to the base of <span class="hlt">ice</span> shelves. On parts of the Amery <span class="hlt">Ice</span> Shelf, frozen <span class="hlt">seawater</span> contributes up to one-third of the <span class="hlt">ice</span>-shelf thickness. Many of the icebergs produced by the Amery are therefore composite icebergs; the upper part consists of meteoric glacier <span class="hlt">ice</span> from snowfall, but the lower part is frozen <span class="hlt">seawater</span> ("marine <span class="hlt">ice</span>"). When these icebergs capsize, the marine <span class="hlt">ice</span> is exposed to view; it can be accessed for study in springtime when the icebergs are embedded in shorefast sea <span class="hlt">ice</span>. The marine <span class="hlt">ice</span> varies in color from blue to green depending on the content of dissolved organic matter. The color is therefore an indicator of biological productivity in the <span class="hlt">seawater</span> from which the <span class="hlt">ice</span> froze. To infer processes at the <span class="hlt">ice</span>-shelf base, these icebergs may be examined and cored for spectral reflectance, hydrogen and oxygen isotopes, organic matter, particles, and distribution of cracks and stripes. Seasonal and interannual variations may be quantified from samples collected along the marine <span class="hlt">ice</span>-growth trajectory at the meteoric/marine-<span class="hlt">ice</span> interface. The scale of small turbulent eddies at the <span class="hlt">ice</span>-shelf base, which govern the transfer of heat between ocean and <span class="hlt">ice</span>, can be inferred from the size of scallops in the iceberg surface (typically a few centimeters). Dark stripes within meteoric <span class="hlt">ice</span> result from tension-cracks at the grounding line, forming basal crevasses that fill suddenly with <span class="hlt">seawater</span>; their width, spacing, and salinity can give clues to processes at the grounding line. Results will be shown from icebergs sampled on Australian expeditions near Davis and Mawson stations. Marine <span class="hlt">ice</span> is more readily accessed by sampling an iceberg than by drilling through an <span class="hlt">ice</span> shelf</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19850029353&hterms=Henry+constant&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3DHenry%2Bconstant','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19850029353&hterms=Henry+constant&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3DHenry%2Bconstant"><span>Henry's law constants for dimethylsulfide in freshwater and <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Dacey, J. W. H.; Wakeham, S. G.; Howes, B. L.</p> <p>1984-01-01</p> <p>Distilled water and several waters of varying salinity were subjected, over a 0-32 C temperature range, to measurements for Henry's law constants for dimethylsulfide. Values for distilled water and <span class="hlt">seawater</span> of the solubility parameters A and C are obtained which support the concept that the concentration of dimethylsulfide in the atmosphere is far from equilibrium with <span class="hlt">seawater</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.C13C0833H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.C13C0833H"><span>A New Fast, Reliable Technique for the Sampling of Dissolved Inorganic Carbon in Sea <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hu, Y.; Wang, F.; Rysgaard, S.; Barber, D. G.</p> <p>2015-12-01</p> <p>For a long time, sea <span class="hlt">ice</span> was considered to act as a lid over <span class="hlt">seawater</span> preventing CO2 exchange between the atmosphere and ocean. Recent observations suggest that sea <span class="hlt">ice</span> can be an active source or a sink for CO2, although its magnitude is not very clear. The direct measurements on CO2 flux based on the chamber method and eddy covariance often do not agree with each other. It is therefore important to measure the dissolved inorganic carbon (DIC) stock in sea <span class="hlt">ice</span> precisely in order to better understand the CO2 flux through sea <span class="hlt">ice</span>. The challenges in sea <span class="hlt">ice</span> DIC sampling is how to melt the <span class="hlt">ice</span> core without being exposed to the air gaining or losing CO2. A common practice is to seal the <span class="hlt">ice</span> core in a self-prepared gas-tight plastic bag and suck the air out of the bag gently using a syringe (together with a needle) through a valve mounted on one side of the bag. However, this method is time consuming (takes up to several minutes to suck the air out) and very often there is large headspace found in the bag after the <span class="hlt">ice</span> melts due to the imperfect bag-preparation, which might affect the DIC concentration in melt <span class="hlt">ice</span>-water. We developed a new technique by using a commercially available plastic bag with a vacuum sealer to seal the <span class="hlt">ice</span> core. In comparison to syringe-based method, this technique is fast and easy to operate; it takes less than 10 seconds to vacuum and seal the bag all in one button with no headspace left in the bag. Experimental tests with replicate <span class="hlt">ice</span> cores sealed by those two methods showed that there is no difference in the DIC concentration measured after these two methods, suggesting that there is no loss of DIC during the course of vacuum sealing. In addition, a time series experiment on DIC in melt <span class="hlt">ice</span>-water stored in the new bag shows that when the samples were not poisoned, the DIC concentration remains unchanged for at least 3 days in the bag; while poisoned by HgCl2, there is no change in DIC for at least 21 days, indicating that this new bag is</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_15");'>15</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li class="active"><span>17</span></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_17 --> <div id="page_18" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="341"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..1812233E','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..1812233E"><span>Properties of meso-Erythritol; phase state, accommodation coefficient and saturation <span class="hlt">vapour</span> pressure</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Emanuelsson, Eva; Tschiskale, Morten; Bilde, Merete</p> <p>2016-04-01</p> <p>Introduction Saturation <span class="hlt">vapour</span> pressure and the associated temperature dependence (enthalpy ΔH), are key parameters for improving predictive atmospheric models. Generally, the atmospheric aerosol community lack experimentally determined values of these properties for relevant organic aerosol compounds (Bilde et al., 2015). In this work we have studied the organic aerosol component meso-Erythritol. Methods Sub-micron airborne particles of meso-Erythritol were generated by nebulization from aqueous solution, dried, and a mono disperse fraction of the aerosol was selected using a differential mobility analyser. The particles were then allowed to evaporate in the ARAGORN (AaRhus Atmospheric Gas phase OR Nano particle) flow tube. It is a temperature controlled 3.5 m long stainless steel tube with an internal diameter of 0.026 m (Bilde et al., 2003, Zardini et al., 2010). Changes in particle size as function of evaporation time were determined using a scanning mobility particle sizer system. Physical properties like air flow, temperature, humidity and pressure were controlled and monitored on several places in the setup. The saturation <span class="hlt">vapour</span> pressures were then inferred from the experimental results in the MATLAB® program AU_VaPCaP (Aarhus University_<span class="hlt">Vapour</span> Pressure Calculation Program). Results Following evaporation, meso-Erythriol under some conditions showed a bimodal particle size distribution indicating the formation of particles of two different phase states. The issue of physical phase state, along with critical assumptions e.g. the accommodation coefficient in the calculations of saturation <span class="hlt">vapour</span> pressures of atmospheric relevant compounds, will be discussed. Saturation <span class="hlt">vapour</span> pressures from the organic compound meso-Erythritol will be presented at temperatures between 278 and 308 K, and results will be discussed in the context of atmospheric chemistry. References Bilde, M. et al., (2015), Chemical Reviews, 115 (10), 4115-4156. Bilde, M. et. al., (2003</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70036486','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70036486"><span><span class="hlt">Seawater</span> calcium isotope ratios across the Eocene-Oligocene transition</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Griffith, E.M.; Paytan, A.; Eisenhauer, A.; Bullen, T.D.; Thomas, E.</p> <p>2011-01-01</p> <p>During the Eocene-Oligocene transition (EOT, ca. 34 Ma), Earth's climate cooled significantly from a greenhouse to an icehouse climate, while the calcite (CaCO3) compensation depth (CCD) in the Pacific Ocean increased rapidly. Fluctuations in the CCD could result from various processes that create an imbalance between calcium (Ca) sources to, and sinks from, the ocean (e.g., weathering and CaCO3 deposition), with different effects on the isotopic composition of dissolved Ca in the oceans due to differences in the Ca isotopic composition of various inputs and outputs. We used Ca isotope ratios (??44/40Ca) of coeval pelagic marine barite and bulk carbonate to evaluate changes in the marine Ca cycle across the EOT. We show that the permanent deepening of the CCD was not accompanied by a pronounced change in <span class="hlt">seawater</span> ??44/40Ca, whereas time intervals in the Neogene with smaller carbonate depositional changes are characterized by <span class="hlt">seawater</span> ??44/40Ca shifts. This suggests that the response of <span class="hlt">seawater</span> ??44/40Ca to changes in weathering fluxes and to imbalances in the oceanic alkalinity budget depends on the chemical composition of <span class="hlt">seawater</span>. A minor and transient fluctuation in the Ca isotope ratio of bulk carbonate may reflect a change in isotopic fractionation associated with CaCO3 precipitation from <span class="hlt">seawater</span> due to a combination of factors, including changes in temperature and/or in the assemblages of calcifying organisms. ?? 2011 Geological Society of America.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70019695','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70019695"><span>Biogeochemical effects of <span class="hlt">seawater</span> restoration to diked salt marshes</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Portnoy, J.W.; Giblin, A.E.</p> <p>1997-01-01</p> <p>We conducted greenhouse microcosm experiments to examine the biogeochemical effects of restoring <span class="hlt">seawater</span> to historically diked Cape Cod salt marshes. Peat cores from both seasonally flooded and drained diked marshes were waterlogged with <span class="hlt">seawater</span>, and porewater chemistry was subsequently monitored for 21 mo. The addition of <span class="hlt">seawater</span> to highly organic, seasonally flooded peat caused the death of freshwater wetland plants, 6-8 cm of sediment subsidence, and increased N and P mineralization. Also, sulfides and alkalinity increased 10-fold, suggesting accelerated decomposition by sulfate reduction. Addition of <span class="hlt">seawater</span> to the low-organic-content acidic peat from the drained marsh increased porewater pH, alkalinity, PO4-P, and Fe(II), which we attribute to the reestablishment of SO4 and Fe(III) mineral reduction. Increased cation exchange contributed to 6-fold increases in dissolved Fe(II) and Al and 60-fold increases in NH4-N within 6 mo of sail-nation. <span class="hlt">Seawater</span> reintroductions to seasonally flooded diked marshes will cause porewater sulfides to increase, likely reducing the success of revegetation efforts. Sulfide toxicity is of less concern in resalinated drained peats because of the abundance of Fe(II) to precipitate sulfides, and of NH4-N to offset sulfide inhibition of N uptake. Restoration of either seasonally flooded or drained diked marshes could stimulate potentially large nutrient and Fe(II) releases, which could in turn increase primary production and lower oxygen in receiving waters. These findings suggest that tidal restoration be gradual and carefully monitored.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2657028','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2657028"><span>Comparisons of Cubed <span class="hlt">Ice</span>, Crushed <span class="hlt">Ice</span>, and Wetted <span class="hlt">Ice</span> on Intramuscular and Surface Temperature Changes</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Dykstra, Joseph H; Hill, Holly M; Miller, Michael G; Cheatham, Christopher C; Michael, Timothy J; Baker, Robert J</p> <p>2009-01-01</p> <p>Context: Many researchers have investigated the effectiveness of different types of cold application, including cold whirlpools, <span class="hlt">ice</span> packs, and chemical packs. However, few have investigated the effectiveness of different types of <span class="hlt">ice</span> used in <span class="hlt">ice</span> packs, even though <span class="hlt">ice</span> is one of the most common forms of cold application. Objective: To evaluate and compare the cooling effectiveness of <span class="hlt">ice</span> packs made with cubed, crushed, and wetted <span class="hlt">ice</span> on intramuscular and skin surface temperatures. Design: Repeated-measures counterbalanced design. Setting: Human performance research laboratory. Patients or Other Participants: Twelve healthy participants (6 men, 6 women) with no history of musculoskeletal disease and no known preexisting inflammatory conditions or recent orthopaedic injuries to the lower extremities. Intervention(s): <span class="hlt">Ice</span> packs made with cubed, crushed, or wetted <span class="hlt">ice</span> were applied to a standardized area on the posterior aspect of the right gastrocnemius for 20 minutes. Each participant was given separate <span class="hlt">ice</span> pack treatments, with at least 4 days between treatment sessions. Main Outcome Measure(s): Cutaneous and intramuscular (2 cm plus one-half skinfold measurement) temperatures of the right gastrocnemius were measured every 30 seconds during a 20-minute baseline period, a 20-minute treatment period, and a 120-minute recovery period. Results: Differences were observed among all treatments. Compared with the crushed-<span class="hlt">ice</span> treatment, the cubed-<span class="hlt">ice</span> and wetted-<span class="hlt">ice</span> treatments produced lower surface and intramuscular temperatures. Wetted <span class="hlt">ice</span> produced the greatest overall temperature change during treatment and recovery, and crushed <span class="hlt">ice</span> produced the smallest change. Conclusions: As administered in our protocol, wetted <span class="hlt">ice</span> was superior to cubed or crushed <span class="hlt">ice</span> at reducing surface temperatures, whereas both cubed <span class="hlt">ice</span> and wetted <span class="hlt">ice</span> were superior to crushed <span class="hlt">ice</span> at reducing intramuscular temperatures. PMID:19295957</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24681371','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24681371"><span>Characterization of aqueous interactions of copper-doped phosphate-based glasses by <span class="hlt">vapour</span> sorption.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Stähli, Christoph; Shah Mohammadi, Maziar; Waters, Kristian E; Nazhat, Showan N</p> <p>2014-07-01</p> <p>Owing to their adjustable dissolution properties, phosphate-based glasses (PGs) are promising materials for the controlled release of bioinorganics, such as copper ions. This study describes a <span class="hlt">vapour</span> sorption method that allowed for the investigation of the kinetics and mechanisms of aqueous interactions of PGs of the formulation 50P2O5-30CaO-(20-x)Na2O-xCuO (x=0, 1, 5 and 10mol.%). Initial characterization was performed using (31)P magic angle spinning nuclear magnetic resonance and attenuated total reflectance-Fourier transform infrared spectroscopy. Increasing CuO content resulted in chemical shifts of the predominant Q(2) NMR peak and of the (POP)as and (PO(-)) Fourier transform infrared absorptions, owing to the higher strength of the POCu bond compared to PONa. <span class="hlt">Vapour</span> sorption and desorption were gravimetrically measured in PG powders exposed to variable relative humidity (RH). Sorption was negligible below 70% RH and increased exponentially with RH from 70 to 90%, where it exhibited a negative correlation with CuO content. <span class="hlt">Vapour</span> sorption in 0% and 1% CuO glasses resulted in phosphate chain hydration and hydrolysis, as evidenced by protonated Q(0)(1H) and Q(1)(1H) species. Dissolution rates in deionized water showed a linear correlation (R(2)>0.99) with <span class="hlt">vapour</span> sorption. Furthermore, cation release rates could be predicted based on dissolution rates and PG composition. The release of orthophosphate and short polyphosphate species corroborates the action of hydrolysis and was correlated with pH changes. In conclusion, the agreement between <span class="hlt">vapour</span> sorption and routine characterization techniques in water demonstrates the potential of this method for the study of PG aqueous reactions. Copyright © 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010JPhD...43b2001S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010JPhD...43b2001S"><span>FAST TRACK COMMUNICATION: Metal <span class="hlt">vapour</span> causes a central minimum in arc temperature in gas-metal arc welding through increased radiative emission</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Schnick, M.; Füssel, U.; Hertel, M.; Spille-Kohoff, A.; Murphy, A. B.</p> <p>2010-01-01</p> <p>A computational model of the argon arc plasma in gas-metal arc welding (GMAW) that includes the influence of metal <span class="hlt">vapour</span> from the electrode is presented. The occurrence of a central minimum in the radial distributions of temperature and current density is demonstrated. This is in agreement with some recent measurements of arc temperatures in GMAW, but contradicts other measurements and also the predictions of previous models, which do not take metal <span class="hlt">vapour</span> into account. It is shown that the central minimum is a consequence of the strong radiative emission from the metal <span class="hlt">vapour</span>. Other effects of the metal <span class="hlt">vapour</span>, such as the flux of relatively cold <span class="hlt">vapour</span> from the electrode and the increased electrical conductivity, are found to be less significant. The different effects of metal <span class="hlt">vapour</span> in gas-tungsten arc welding and GMAW are explained.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.C11B0758J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.C11B0758J"><span>Imaging Basal Crevasses at the Grounding Line of Whillans <span class="hlt">Ice</span> Stream, West Antarctica</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Jacobel, R. W.; Dawson, E. C.; Christianson, K.</p> <p>2015-12-01</p> <p>We acquired gridded ground-based radar data at the WIS grounding zone where the transition from limited- or no-slip conditions at the base of grounded <span class="hlt">ice</span> to free-slip conditions beneath floating <span class="hlt">ice</span> occurs across a region only a few kilometers wide. This transition is either an elastic-flexural transition from bedrock to hydrostatically-supported elevations (often tidally influenced), a transition from thicker to thinner <span class="hlt">ice</span> over a flat bed, or some combination of these. In either case, the stress field of the <span class="hlt">ice</span> changes as it flows across the grounding zone, often resulting in brittle deformation, which is manifested as basal crevassing at the <span class="hlt">ice</span>-sheet base and sometimes as strand cracks at the surface. The position and morphology of these features reveal important information about the stress state across this transition where <span class="hlt">ice</span> and ocean interact. Our surveys indicate a complex pattern of basal crevassing with many imaged in two or more profile segments as a linear feature at the bed, usually trending oblique to flow and often extending for several kilometers. Due to the wide beam pattern of our antennas, we image many of the crevasses from off-nadir reflections. Thus their arrival times are later than the primary basal reflection and segments of the crevasse appear "below" the bed, when in fact they are merely trending oblique to the profile. Often these returns have a reversed phase relative to the bed echo because the high dielectric contrast of <span class="hlt">seawater</span> and a favorable geometry enable reflections with little loss (but a second phase reversal) from the <span class="hlt">ice</span>-water interface near the crevasse base. In a few cases, these crevasse echoes from targets trending oblique to the profile appear to mimic the geometry of a sub-<span class="hlt">ice</span> sediment "wedge", while in reality the radar never penetrates below the basal interface. Only about 25% of the crevasses appear to extend any significant distance upward into the basal <span class="hlt">ice</span>, typically at low angles. A subset of these are</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28850131','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28850131"><span>Real-time fluorescence quenching-based detection of nitro-containing explosive <span class="hlt">vapours</span>: what are the key processes?</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Shaw, P E; Burn, P L</p> <p>2017-11-15</p> <p>The detection of explosives continues to be a pressing global challenge with many potential technologies being pursued by the scientific research community. Luminescence-based detection of explosive <span class="hlt">vapours</span> with an organic semiconductor has attracted much interest because of its potential for detectors that have high sensitivity, compact form factor, simple operation and low-cost. Despite the abundance of literature on novel sensor materials systems there are relatively few mechanistic studies targeted towards <span class="hlt">vapour</span>-based sensing. In this Perspective, we will review the progress that has been made in understanding the processes that control the real-time luminescence quenching of thin films by analyte <span class="hlt">vapours</span>. These are the non-radiative quenching process by which the sensor exciton decays, the analyte-sensor intermolecular binding interaction, and the diffusion process for the analyte <span class="hlt">vapours</span> in the film. We comment on the contributions of each of these processes towards the sensing response and, in particular, the relative roles of analyte diffusion and exciton diffusion. While the latter has been historically judged to be one of, if not the primary, causes for the high sensitivity of many conjugated polymers to nitrated <span class="hlt">vapours</span>, recent evidence suggests that long exciton diffusion lengths are unnecessary. The implications of these results on the development of sensor materials for real-time detection are discussed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25189478','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25189478"><span>An exploratory study on <span class="hlt">seawater</span>-catalysed urine phosphorus recovery (SUPR).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Dai, Ji; Tang, Wen-Tao; Zheng, Yi-Se; Mackey, Hamish R; Chui, Ho Kwong; van Loosdrecht, Mark C M; Chen, Guang-Hao</p> <p>2014-12-01</p> <p>Phosphorus (P) is a crucial and non-renewable resource, while it is excessively discharged via sewage, significant amounts originating from human urine. Recovery of P from source-separated urine presents an opportunity not only to recover this precious resource but also to improve downstream sewage treatment works. This paper proposes a simple and economic method to recover urine derived P by using <span class="hlt">seawater</span> as a low-cost precipitant to form struvite, as Hong Kong has practised <span class="hlt">seawater</span> toilet flushing as an alternative water resource since 1958. Chemical reactions, process conditions and precipitate composition for P precipitation in urine have been investigated to develop this new urine P recovery approach. This study concluded that ureolysis extent in a urine-<span class="hlt">seawater</span> mixture determines the reaction pH that in turn influences the P recovery efficiency significantly; 98% of urine P can precipitate with <span class="hlt">seawater</span> within 10 min when 40-75% of the urea in urine is ureolysed; the urine to <span class="hlt">seawater</span> ratio alters the composition of the precipitates. The P content in the precipitates was found to be more than 9% when the urine fraction was 40% or higher. Magnesium ammonium phosphate (MAP) was confirmed to be the predominant component of the precipitates. Copyright © 2014 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25689216','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25689216"><span>XAS and TRLIF spectroscopy of uranium and neptunium in <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Maloubier, Melody; Solari, Pier Lorenzo; Moisy, Philippe; Monfort, Marguerite; Den Auwer, Christophe; Moulin, Christophe</p> <p>2015-03-28</p> <p><span class="hlt">Seawater</span> contains radionuclides at environmental levels; some are naturally present and others come from anthropogenic nuclear activity. In this report, the molecular speciation in <span class="hlt">seawater</span> of uranium(VI) and neptunium(V) at a concentration of 5 × 10(-5) M has been investigated for the first time using a combination of two spectroscopic techniques: Time-resolved laser-induced fluorescence (TRLIF) for U and extended X-ray absorption fine structure (EXAFS) for U and Np at the LIII edge. In parallel, the theoretical speciation of uranium and neptunium in <span class="hlt">seawater</span> at the same concentration is also discussed and compared to spectroscopic data. The uranium complex was identified as the neutral carbonato calcic complex UO2(CO3)3Ca2, which has been previously described in other natural systems. In the case of neptunium, the complex identified is mainly a carbonato complex whose exact stoichiometry is more difficult to assess. The knowledge of the actinide molecular speciation and reactivity in <span class="hlt">seawater</span> is of fundamental interest in the particular case of uranium recovery and more generally regarding the actinide life cycle within the biosphere in the case of accidental release. This is the first report of actinide direct speciation in <span class="hlt">seawater</span> medium that can complement inventory data.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1999NIMPA.432..505N','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1999NIMPA.432..505N"><span>Solid-state detector system for measuring concentrations of tritiated water <span class="hlt">vapour</span> and other radioactive gases</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Nunes, J. C.; Surette, R. A.; Wood, M. J.</p> <p>1999-08-01</p> <p>A detector system was built using a silicon photodiode plus preamplifier and a cesium iodide scintillator plus preamplifier that were commercially available. The potential of the system for measuring concentrations of tritiated water <span class="hlt">vapour</span> in the presence of other radioactive sources was investigated. For purposes of radiation protection, the sensitivity of the detector system was considered too low for measuring tritiated water <span class="hlt">vapour</span> concentrations in workplaces such as nuclear power plants. Nevertheless, the spectrometry capability of the system was used successfully to differentiate amongst some radioactive gases in laboratory tests. Although this relatively small system can measure radioactive noble gases as well as tritiated water <span class="hlt">vapour</span> concentrations, its response to photons remains an issue.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2010AGUFM.B51G0422J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2010AGUFM.B51G0422J"><span>Recalibrating the concentration of Precambrian <span class="hlt">seawater</span> sulfate</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Johnston, D. T.; Bradley, A. S.; Hoarfrost, A.; Girguis, P. R.</p> <p>2010-12-01</p> <p>The isotopic offset between sulfate sulfur and sulfide sulfur (δ34Ssulfate-sulfide) is widely used in the Precambrian as a paleo-indicator of <span class="hlt">seawater</span> sulfate concentrations. Popularized by experimental work proposing an increase in <span class="hlt">seawater</span> sulfate at the Archean - Proterozoic boundary, the concept of using a calibrated physiological process (dissimilatory sulfate reduction) to extract environmental information holds the potential to unlock numerous geological questions. To that end, the interpretability of sulfur isotope records relies on the degree to which strict quantitative constraints have been placed on the relationship between sulfate concentrations and sulfate reducing bacteria. Our work serves to extend those constraints. Here we present data from a series of replicate quasi-chemostat microbial reactors, inoculated with marine sediment from Monterey Bay and incubated with artificial <span class="hlt">seawater</span> ([SO42-]< 5 mM). Our experimental design continuously removes sulfide and allows for systematic tracking of the dependence of δ34Ssulfate-sulfide on <span class="hlt">seawater</span> sulfate concentration. In addition to expanding the existing δ34S context, we target high-precision multiple sulfur isotope data, which allows for a greater interpretability of both the overall result and its mapping onto environmental records. Further, we use natural abundance and δ18O spiked water within our experiments to assay rates of cellular re-oxidation (within the sulfate reduction pathway) and to constrain natural δ18O effects within these systems. Finally, we use modern molecular biological techniques to track community structure as a function of time and environmental conditions. Together, these data provide an integrated metric with which to interpret complex natural sulfur isotope records.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26319611','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26319611"><span>Cultivation of oleaginous Rhodotorula mucilaginosa in airlift bioreactor by using <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Yen, Hong-Wei; Liao, Yu-Ting; Liu, Yi Xian</p> <p>2016-02-01</p> <p>The enormous water resource consumption is a concern to the scale-up fermentation process, especially for those cheap fermentation commodities, such as microbial oils as the feedstock for biodiesel production. The direct cultivation of oleaginous Rhodotorula mucilaginosa in a 5-L airlift bioreactor using <span class="hlt">seawater</span> instead of pure water led to a slightly lower biomass being achieved, at 17.2 compared to 18.1 g/L, respectively. Nevertheless, a higher lipid content of 65 ± 5% was measured in the batch using <span class="hlt">seawater</span> as compared to the pure water batch. Both the salinity and osmotic pressure decreased as the cultivation time increased in the <span class="hlt">seawater</span> batch, and these effects may contribute to the high tolerance for salinity. No effects were observed for the <span class="hlt">seawater</span> on the fatty acid profiles. The major components for both batches using <span class="hlt">seawater</span> and pure water were C16:0 (palmitic acid), C18:1 (oleic acid) and C18:2 (linoleic acid), which together accounted for over 85% of total lipids. The results of this study indicated that <span class="hlt">seawater</span> could be a suitable option for scaling up the growth of oleaginous R. mucilaginosa, especially from the perspective of water resource utilization. Copyright © 2015 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16864138','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16864138"><span>Effects of using slurry <span class="hlt">ice</span> during transportation on the microbiological, chemical, and sensory assessments of aquacultured sea bass (Dicentrarchus labrax) stored at 4 degrees C.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Cakli, Sukran; Kilinc, Berna; Dincer, Tolga; Tolasa, Sebnem</p> <p>2006-01-01</p> <p>Slurry <span class="hlt">ice</span>, a biphasic system consisting of small spherical <span class="hlt">ice</span> crystals surrounded by <span class="hlt">seawater</span> at subzero temperature, was evaluated as a new chilled storage method for whole sea bass (Dicentrarchus labrax) a sparidae fish species of remarkable commercial interests. In this study two different group of chilling methods were used during transportation; in slurry <span class="hlt">ice</span> packaged (Group A), and flake <span class="hlt">ice</span> packaged (Group B). The effect of this advanced system during transportation on quality losses and the shelf life of aquacultured sea bass was evaluated. Mesophilic counts for sea bass exceeded 7 log cfu/g, which is considered the maximum level for acceptability for freshwater and marine fish after 13 days for groups A and B. On day 13 TVB-N values of groups A and B, reached the legal limits (35 mg/100 g set for TVB-N) for consumption. According to the results of sensory analyses, up to day 9 all the groups were determined as "acceptable" but on day 13 the groups A and B were no longer acceptable. The main negative aspect related to quality loss in slurry <span class="hlt">ice</span> group corresponded to the appearance of eyes and gills. Using slurry <span class="hlt">ice</span> during transportation did not extend the shelf life of sea bass stored at 4 degrees C.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016E%26PSL.438..139E','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016E%26PSL.438..139E"><span>Planktic foraminifera shell chemistry response to <span class="hlt">seawater</span> chemistry: Pliocene-Pleistocene <span class="hlt">seawater</span> Mg/Ca, temperature and sea level change</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Evans, David; Brierley, Chris; Raymo, Maureen E.; Erez, Jonathan; Müller, Wolfgang</p> <p>2016-03-01</p> <p>Foraminifera Mg/Ca paleothermometry forms the basis of a substantial portion of ocean temperature reconstruction over the last 5 Ma. Furthermore, coupled Mg/Ca-oxygen isotope (δ18O) measurements of benthic foraminifera can constrain eustatic sea level (ESL) independent of paleo-shoreline derived approaches. However, this technique suffers from uncertainty regarding the secular variation of the Mg/Ca <span class="hlt">seawater</span> ratio (Mg/Casw) on timescales of millions of years. Here we present coupled <span class="hlt">seawater</span>-test Mg/Ca-temperature laboratory calibrations of Globigerinoides ruber in order to test the widely held assumptions that (1) <span class="hlt">seawater</span>-test Mg/Ca co-vary linearly, and (2) the Mg/Ca-temperature sensitivity remains constant with changing Mg/Casw. We find a nonlinear Mg/Catest-Mg/Casw relationship and a lowering of the Mg/Ca-temperature sensitivity at lower than modern Mg/Casw from 9.0% °C-1 at Mg/Casw = 5.2 mol mol-1 to 7.5 ± 0.9% °C-1 at 3.4 mol mol-1. Using our calibrations to more accurately calculate the offset between Mg/Ca and biomarker-derived paleotemperatures for four sites, we derive a Pliocene Mg/Casw ratio of ∼4.3 mol mol-1. This Mg/Casw implies Pliocene ocean temperature 0.9-1.9 °C higher than previously reported and, by extension, ESL ∼30 m lower compared to when one assumes that Pliocene Mg/Casw is the same as at present. Correcting existing benthic foraminifera datasets for Mg/Casw indicates that deep water source composition must have changed through time, therefore <span class="hlt">seawater</span> oxygen isotope reconstructions relative to present day cannot be used to directly reconstruct Pliocene ESL.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015E%26PSL.425..219B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015E%26PSL.425..219B"><span>Gradients in seasonality and <span class="hlt">seawater</span> oxygen isotopic composition along the early Permian Gondwanan coast, SE Australia</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Beard, J. Andrew; Ivany, Linda C.; Runnegar, Bruce</p> <p>2015-09-01</p> <p>, suggesting comparatively lower salinity water or more O18-depleted glacial <span class="hlt">ice</span>/runoff in the Permian Gondwanan high latitudes, perhaps augmented by more depleted (negative) global average <span class="hlt">seawater</span>. Conditions in southeastern Australia during the largest of the Permian deglaciations were warmer than present-day Antarctica at similar latitudes, but may approximate those of early-mid Miocene Antarctica, with frozen winters but summers closer to 10 °C.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25378621','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25378621"><span>Sulfate was a trace constituent of Archean <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Crowe, Sean A; Paris, Guillaume; Katsev, Sergei; Jones, CarriAyne; Kim, Sang-Tae; Zerkle, Aubrey L; Nomosatryo, Sulung; Fowle, David A; Adkins, Jess F; Sessions, Alex L; Farquhar, James; Canfield, Donald E</p> <p>2014-11-07</p> <p>In the low-oxygen Archean world (>2400 million years ago), <span class="hlt">seawater</span> sulfate concentrations were much lower than today, yet open questions frustrate the translation of modern measurements of sulfur isotope fractionations into estimates of Archean <span class="hlt">seawater</span> sulfate concentrations. In the water column of Lake Matano, Indonesia, a low-sulfate analog for the Archean ocean, we find large (>20 per mil) sulfur isotope fractionations between sulfate and sulfide, but the underlying sediment sulfides preserve a muted range of δ(34)S values. Using models informed by sulfur cycling in Lake Matano, we infer Archean <span class="hlt">seawater</span> sulfate concentrations of less than 2.5 micromolar. At these low concentrations, marine sulfate residence times were likely 10(3) to 10(4) years, and sulfate scarcity would have shaped early global biogeochemical cycles, possibly restricting biological productivity in Archean oceans. Copyright © 2014, American Association for the Advancement of Science.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.B13F0697C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.B13F0697C"><span>Arctic sea <span class="hlt">ice</span>: an investigation into the origin of nitrate using δ15N, δ18O and Δ17O</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Clark, S. C.; Mastorakis, A.; Granger, J.; Aguilar-Islas, A. M.; Hastings, M. G.</p> <p>2016-12-01</p> <p>Nitrogen (N) is essential to primary production and is made bioavailable through N2-fixation, and potentially, atmospheric deposition. While the Pacific delivers a significant supply of reactive N to the Arctic, it is unclear if atmospheric deposition helps fuel primary production in the N-deplete western Arctic Ocean. Sea <span class="hlt">ice</span> and snow provide a unique opportunity to partition the end-member contributions of nitrate (NO3-) from the atmosphere to the ocean. Sea <span class="hlt">ice</span> cores and snow samples were collected at six stations between 82 and 89°N as part of the U.S. Arctic GEOTRACES expedition in 2015. Sea <span class="hlt">ice</span> samples had NO3- concentrations ranging from 0.2-1.0 µmol L-1 while snow samples were slightly higher ranging from 1.1-3.7 µmol L-1. The complete isotopic composition of NO3- (δ15N, δ18O, Δ17O) was measured using the denitrifier method on all snow samples and 32 core sub-samples. The Δ17O (Δ17O=δ17O-0.52*δ18O≠0) is a proven diagnostic tool for atmospheric NO3- compared to other NO3- sources because a nonzero Δ17O originates from the influence of ozone on the formation of NO3- in the atmosphere. Snow samples were characteristic of atmospheric NO3- with generally negative δ15N (-5.9-2‰) and highly enriched 17O and 18O (Δ17O=27.1-33.5‰; δ18O =70.8-87.8‰). In contrast, sea <span class="hlt">ice</span> samples were more enriched in 15N (-0.3-15‰) and depleted in 17O and 18O (Δ17O=0-12.4‰; δ18O=23.3-67.5‰). The presence of a Δ17O>0‰ occurs at various depths, indicating that atmospheric NO3- is an important component of the NO3- found in sea <span class="hlt">ice</span>. However, the lower Δ17O and δ18O values compared to snow suggest that a significant portion of the NO3- is either derived from <span class="hlt">seawater</span> and/or issued from biological cycling of atmospheric/<span class="hlt">seawater</span> reactive N in sea <span class="hlt">ice</span>. Moreover, it appears that atmospheric NO3- is lost or consumed such that this biological processing of NO3- is most prominent. Recent trends in sea <span class="hlt">ice</span> decline may result in future changes to the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4959478','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4959478"><span>Cell Culture Isolation of Piscine Nodavirus (Betanodavirus) in Fish-Rearing <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Nishi, Shinnosuke; Yamashita, Hirofumi; Kawato, Yasuhiko</p> <p>2016-01-01</p> <p>Piscine nodavirus (betanodavirus) is the causative agent of viral nervous necrosis (VNN) in a variety of cultured fish species, particularly marine fish. In the present study, we developed a sensitive method for cell culture isolation of the virus from <span class="hlt">seawater</span> and applied the method to a spontaneous fish-rearing environment. The virus in <span class="hlt">seawater</span> was concentrated by an iron-based flocculation method and subjected to isolation with E-11 cells. A real-time reverse transcriptase PCR (RT-PCR) assay was used to quantify the virus in water. After spiking into <span class="hlt">seawater</span> was performed, a betanodavirus strain (redspotted grouper nervous necrosis virus [RGNNV] genotype) was effectively recovered in the E-11 cells at a detection limit of approximately 105 copies (equivalent to 102 50% tissue culture infective doses [TCID50])/liter <span class="hlt">seawater</span>. In an experimental infection of juvenile sevenband grouper (Epinephelus septemfasciatus) with the virus, the virus was isolated from the drainage of a fish-rearing tank when the virus level in water was at least approximately 105 copies/liter. The application of this method to sevenband grouper-rearing floating net pens, where VNN prevailed, resulted in the successful isolation of the virus from <span class="hlt">seawater</span>. No differences were found in the partial sequences of the coat protein gene (RNA2) between the clinical virus isolates of dead fish and the cell-cultured virus isolates from <span class="hlt">seawater</span>, and the viruses were identified as RGNNV. The infection experiment showed that the virus isolates from <span class="hlt">seawater</span> were virulent to sevenband grouper. These results showed direct evidence of the horizontal transmission of betanodavirus via rearing water in marine aquaculture. PMID:26896128</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016GBioC..30.1038L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016GBioC..30.1038L"><span>Benthic marine calcifiers coexist with CaCO3-undersaturated <span class="hlt">seawater</span> worldwide</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lebrato, M.; Andersson, A. J.; Ries, J. B.; Aronson, R. B.; Lamare, M. D.; Koeve, W.; Oschlies, A.; Iglesias-Rodriguez, M. D.; Thatje, S.; Amsler, M.; Vos, S. C.; Jones, D. O. B.; Ruhl, H. A.; Gates, A. R.; McClintock, J. B.</p> <p>2016-07-01</p> <p>Ocean acidification and decreasing <span class="hlt">seawater</span> saturation state with respect to calcium carbonate (CaCO3) minerals have raised concerns about the consequences to marine organisms that build CaCO3 structures. A large proportion of benthic marine calcifiers incorporate Mg2+ into their skeletons (Mg-calcite), which, in general, reduces mineral stability. The relative vulnerability of some marine calcifiers to ocean acidification appears linked to the relative solubility of their shell or skeletal mineralogy, although some organisms have sophisticated mechanisms for constructing and maintaining their CaCO3 structures causing deviation from this dependence. Nevertheless, few studies consider <span class="hlt">seawater</span> saturation state with respect to the actual Mg-calcite mineralogy (ΩMg-x) of a species when evaluating the effect of ocean acidification on that species. Here, a global dataset of skeletal mole % MgCO3 of benthic calcifiers and in situ environmental conditions spanning a depth range of 0 m (subtidal/neritic) to 5600 m (abyssal) was assembled to calculate in situ ΩMg-x. This analysis shows that 24% of the studied benthic calcifiers currently experience <span class="hlt">seawater</span> mineral undersaturation (ΩMg-x < 1). As a result of ongoing anthropogenic ocean acidification over the next 200 to 3000 years, the predicted decrease in <span class="hlt">seawater</span> mineral saturation will expose approximately 57% of all studied benthic calcifying species to <span class="hlt">seawater</span> undersaturation. These observations reveal a surprisingly high proportion of benthic marine calcifiers exposed to <span class="hlt">seawater</span> that is undersaturated with respect to their skeletal mineralogy, underscoring the importance of using species-specific <span class="hlt">seawater</span> mineral saturation states when investigating the impact of CO2-induced ocean acidification on benthic marine calcification.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_16");'>16</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li class="active"><span>18</span></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_18 --> <div id="page_19" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="361"> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1994GeoRL..21.1523H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1994GeoRL..21.1523H"><span>Formation of formic acid and organic peroxides in the ozonolysis of ethene with added water <span class="hlt">vapour</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Horie, Osamu; Neeb, Peter; Limbach, Stefan; Moortgat, Geert K.</p> <p>1994-07-01</p> <p>Ozonolysis of C2H4 was carried out in a 580 l glass reaction vessel at 1-5 ppm reactant concentrations, with added water <span class="hlt">vapour</span>. Under dry conditions ([H2O]0 = 0.5 ppm), HCHO, CO, CO2, (CHO)2O (formic acid anhydride), H2O2, and CH3OOH were identified as the reaction products. Under wet conditions ([H2O]0 = 2 × 104 ppm), HCOOH yields approaching ca. 20% of the converted C2H4, were observed, while no (CHO)2O was formed. Hydroxymethyl hydroperoxide, HOCH2OOH, was observed as the major peroxide, and found to be formed only in the presence of water <span class="hlt">vapour</span>. Direct reactions of H2O <span class="hlt">vapour</span> with the excited CH2OO* radicals and with stabilized CH2OO radicals are postulated to explain the formation of HCOOH and HOCH2OOH in the presence of water <span class="hlt">vapour</span>, respectively.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005QJRMS.131.2665C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005QJRMS.131.2665C"><span>Water-<span class="hlt">vapour</span> variability within a convective boundary-layer assessed by large-eddy simulations and IHOP_2002 observations</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Couvreux, F.; Guichard, F.; Redelsperger, J. L.; Kiemle, C.; Masson, V.; Lafore, J. P.; Flamant, C.</p> <p>2005-10-01</p> <p>This study presents a comprehensive analysis of the variability of water <span class="hlt">vapour</span> in a growing convective boundary-layer (CBL) over land, highlighting the complex links between advection, convective activity and moisture heterogeneity in the boundary layer. A Large-eddy Simulation (LES) is designed, based on observations, and validated, using an independent data-set collected during the International H2O Project (IHOP 2002) fieldexperiment. Ample information about the moisture distribution in space and time, as well as other important CBL parameters are acquired by mesonet stations, balloon soundings, instruments on-board two aircraft and the DLR airborne water-<span class="hlt">vapour</span> differential-absorption lidar. Because it can deliver two-dimensional cross-sections at high spatial resolution (140 m horizontal, 200 m vertical), the airborne lidar offers valuable insights of small-scale moisture-variability throughout the CBL. The LES is able to reproduce the development of the CBL in the morning and early afternoon, as assessed by comparisons of simulated mean profiles of key meteorological variables with sounding data. Simulated profiles of the variance of water-<span class="hlt">vapour</span> mixing-ratio were found to be in good agreement with the lidar-derived counterparts. Finally, probability-density functions of potential temperature, vertical velocity and water-<span class="hlt">vapour</span> mixing-ratio calculated from the LES show great consistency with those derived from aircraft in situ measurements in the middle of the CBL. Downdraughts entrained from above the CBL are governing the scale of moisture variability. Characteristic length-scales are found to be larger for water-<span class="hlt">vapour</span> mixing-ratio than for temperature.The observed water-<span class="hlt">vapour</span> variability exhibits contributions from different scales. The influence of the mesoscale (larger than LES domain size, i.e. 10 km) on the smaller-scale variability is assessed using LES and observations. The small-scale variability of water <span class="hlt">vapour</span> is found to be important and to be</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA617621','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA617621"><span>Wave-<span class="hlt">Ice</span> and Air-<span class="hlt">Ice</span>-Ocean Interaction During the Chukchi Sea <span class="hlt">Ice</span> Edge Advance</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2014-09-30</p> <p>During cruise CU-B UAF UW Airborne expendable <span class="hlt">Ice</span> Buoy (AXIB) Ahead, at and inside <span class="hlt">ice</span> edge Surface meteorology T, SLP ~1 year CU-B UW...Balance (IMB) buoys Inside <span class="hlt">ice</span> edge w/ >50cm thickness <span class="hlt">Ice</span> mass balance T in snow-<span class="hlt">ice</span>-ocean, T, SLP at surface ~1 year WHOI CRREL (SeaState DRI</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFMOS54A..05D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFMOS54A..05D"><span>Chemical Characteristics of <span class="hlt">Seawater</span> and Sediment in the Yap Trench</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ding, H.; Sun, C.; Yang, G.</p> <p>2017-12-01</p> <p>In June 2016, <span class="hlt">seawater</span> samples at sediment-<span class="hlt">seawater</span> interface and sediment samples were collected by the he Jiaolong, China's manned submersible, at four sampling sites located in the Yap Trench. <span class="hlt">Seawater</span> samples from different depths of the trench were also collected by CTD. Chemical parameters, including pH, alkanility, concentrations of dissolved inorganic carbon, dissolved and total organic carbon, methane, dimethylsulfoniopropionate, nutrients, carbohydrates, and amino acids were analyzed in the <span class="hlt">seawater</span> samples. Concentrations of total organic carbon, six constant elements and nine trace elements were determined in the sediment samples. All the vertical profiles of the chemical parameters in the <span class="hlt">seawater</span> have unique characteristics. Our resluts also showed that the carbonate compensation depth (CCD) was between 4500 m and 5000 m in the trench. The hadal sediment at 6500 m depth under the CCD line was siliceous ooze favored for the burial of orgaic carbon, attributed to accumulation of surface sediment by gravity flow. The abyssal sediment at the 4500 m depth was calcareous ooze. Various microfossils, such as discoasters and diatoms, were identified in different sediment layers of the sediment samples.Based on the ratios of Fe/Al and Ti/Al, and the correlation between different elements, the sediment in the Yap Trench were derived from biogenic, terrestrial, volcanic and autogenic sources. The ratios of Ni/Co and V/Cr showed that the deposition environment of the trench should be oxidative, arributed to inflow of the Antractic bottom oxygen-rich <span class="hlt">seawater</span>.The high concentraiont of Ca in the sediment from the station 371-Yap-S02 below 4 cm depth indicated that there was no large-scale volcanic eruption in the research area and the volcanic materials in the sediment might orginated from the Mariana Volcanic Arc, and the Carolyn Ridge has been slowly sinking on the east side of the trench due to plate subduction. This study is the first systematic study of</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=salinity&pg=2&id=ED261897','ERIC'); return false;" href="https://eric.ed.gov/?q=salinity&pg=2&id=ED261897"><span>Algorithms for Computation of Fundamental Properties of <span class="hlt">Seawater</span>. Endorsed by Unesco/SCOR/<span class="hlt">ICES</span>/IAPSO Joint Panel on Oceanographic Tables and Standards and SCOR Working Group 51. Unesco Technical Papers in Marine Science, No. 44.</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Fofonoff, N. P.; Millard, R. C., Jr.</p> <p></p> <p>Algorithms for computation of fundamental properties of <span class="hlt">seawater</span>, based on the practicality salinity scale (PSS-78) and the international equation of state for <span class="hlt">seawater</span> (EOS-80), are compiled in the present report for implementing and standardizing computer programs for oceanographic data processing. Sample FORTRAN subprograms and tables are given…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015PalOc..30.1437L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015PalOc..30.1437L"><span>Neogene <span class="hlt">ice</span> volume and ocean temperatures: Insights from infaunal foraminiferal Mg/Ca paleothermometry</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lear, Caroline H.; Coxall, Helen K.; Foster, Gavin L.; Lunt, Daniel J.; Mawbey, Elaine M.; Rosenthal, Yair; Sosdian, Sindia M.; Thomas, Ellen; Wilson, Paul A.</p> <p>2015-11-01</p> <p>Antarctic continental-scale glaciation is generally assumed to have initiated at the Eocene-Oligocene Transition, yet its subsequent evolution is poorly constrained. We reconstruct changes in bottom water temperature and global <span class="hlt">ice</span> volume from 0 to 17 Ma using δ18O in conjunction with Mg/Ca records of the infaunal benthic foraminifer, O. umbonatus from Ocean Drilling Program (ODP) Site 806 (equatorial Pacific; ~2500 m). Considering uncertainties in core top calibrations and sensitivity to <span class="hlt">seawater</span> Mg/Ca (Mg/Ca)sw, we produce a range of Mg/Ca-temperature-Mg/Casw calibrations. Our favored exponential temperature calibration is Mg/Ca = 0.66 ± 0.08 × Mg/Casw0.27±0.06 × e(0.114±0.02 × BWT) and our favored linear temperature calibration is Mg/Ca = (1.21 ± 0.04 + 0.12 ± 0.004 × BWT (bottom water temperature)) × (Mg/Casw-0.003±0.02) (stated errors are 2 s.e.). The equations are obtained by comparing O. umbonatus Mg/Ca for a Paleocene-Eocene section from Ocean Drilling Program (ODP) Site 690 (Weddell Sea) to δ18O temperatures, calculated assuming <span class="hlt">ice</span>-free conditions during this peak warmth period of the Cenozoic. This procedure suggests negligible effect of Mg/Casw on the Mg distribution coefficient (DMg). Application of the new equations to the Site 806 record leads to the suggestion that global <span class="hlt">ice</span> volume was greater than today after the Middle Miocene Climate Transition (~14 Ma). ODP Site 806 bottom waters cooled and freshened as the Pacific zonal sea surface temperature gradient increased, and climate cooled through the Pliocene, prior to the Plio-Pleistocene glaciation of the Northern Hemisphere. The records indicate a decoupling of deep water temperatures and global <span class="hlt">ice</span> volume, demonstrating the importance of thresholds in the evolution of the Antarctic <span class="hlt">ice</span> sheet.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2007AcSpe..62..799C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2007AcSpe..62..799C"><span>3D imaging of <span class="hlt">vapour</span> and liquid inclusions from the Mole Granite, Australia, using helical fluorescence tomography</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Cauzid, J.; Philippot, P.; Bleuet, P.; Simionovici, A.; Somogyi, A.; Golosio, B.</p> <p>2007-08-01</p> <p>World class Cu resources are concentrated in porphyry and epithermal ore deposits. Their formation remains partially understood, however, due to a lack of constraints on the partitioning properties of trace elements in general, and Cu in particular, between <span class="hlt">vapour</span> and liquid phases evolved from boiling fluids at depth in the Earth's crust. Immiscible liquid and <span class="hlt">vapour</span> fluid inclusions coexisting in a single quartz grain have been imaged in three dimensions by X-ray Fluorescence Computed Tomography (XFCT). Elemental spatial distributions confirm that Cu, and to a lesser extent As, partition into the <span class="hlt">vapour</span> phase, whereas Mn, Fe, Zn, Br, Rb, Sr and Pb concentrate in the liquid inclusion. High resolution mapping of the <span class="hlt">vapour</span> inclusions revealed that Cu is heterogeneously distributed at the scale of a single inclusion and is mostly concentrated as tiny daughter crystals.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1234341-extracting-uranium-from-seawater-promising-ai-series-adsorbents','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1234341-extracting-uranium-from-seawater-promising-ai-series-adsorbents"><span>Extracting uranium from <span class="hlt">seawater</span>: Promising AI series adsorbents</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Das, Sadananda; Oyola, Y.; Mayes, Richard T.; ...</p> <p>2015-11-10</p> <p>A series of adsorbent (AI10 through AI17) were successfully developed at ORNL by radiation induced graft polymerization (RIGP) of acrylonitrile (AN) and vinylphosphonic acid (VPA) (at different mole/mole ratios) onto high surface area polyethylene fiber, with higher degree of grafting which ranges from 110 300%. The grafted nitrile groups were converted to amidoxime groups by reaction with 10 wt% hydroxylamine at 80 C for 72 hours. The amidoximated adsorbents were then conditioned with 0.44M KOH at 80 C followed by screening at ORNL with simulated <span class="hlt">seawater</span> spiked with 8 ppm uranium. Uranium adsorption capacity in simulated <span class="hlt">seawater</span> screening ranged frommore » 171-187 g-U/kg-ads irrespective of %DOG. The performance of the adsorbents for uranium adsorption in natural <span class="hlt">seawater</span> was also carried out using flow-through-column at Pacific Northwest National Laboratory (PNNL). The three hours KOH conditioning was better for higher uranium uptake than one hour. The adsorbent AI11 containing AN and VPA at the mole ration of 3.52, emerged as the potential candidate for higher uranium adsorption (3.35 g-U/Kg-ads.) after 56 days of exposure in the <span class="hlt">seawater</span> in the flow-through-column. The rate vanadium adsorption over uranium was linearly increased throughout the 56 days exposure. The total vanadium uptake was ~5 times over uranium after 56 days.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1992SedG...77..249Q','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1992SedG...77..249Q"><span>Skeletal aragonite dissolution from hypersaline <span class="hlt">seawater</span>: a hypothesis</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Qing Sun, S.</p> <p>1992-05-01</p> <p>Hypersaline <span class="hlt">seawater</span> has often been invoked as a mechanism to explain the pervasive dolomitization of ancient platform carbonates, but its potential in causing skeletal aragonite dissolution of these carbonates has rarely been investigated. Previous experimental and theoretical studies have demonstrated that hypersaline <span class="hlt">seawater</span> is undersaturated with respect to aragonite when evaporation reaches a certain degree. It is contended here that similar undersaturation could also have occurred in ancient evaporitic seas. Geological evidence from the Miocene carbonates of SE Spain, Gulf of Suez, Red Sea and Iraq suggests that this may have been the case. Despite differences in their geological settings, these carbonates have common diagenetic features including: (1) widespread dissolution of skeletal aragonite with little or no calcite cementation; and (2) pervasive dolomitization. Dolomite occurs as both a replacement of Mg calcite and mouldic pore-filling cement. The association of the dolomites with evaporites, their relatively heavy oxygen isotopic values and widespread distribution suggest a hypersaline <span class="hlt">seawater</span> origin of these dolomites. Petrographic data indicate that skeletal aragonite was dissolved during dolomitization because the aragonite fossil moulds contain dolomite cements, but no pre-dolomitization calcite cements, implying that the dolomitizing fluids (hypersaline <span class="hlt">seawater</span>) were probably undersaturated with respect to aragonite. The dissolved calcium may have been subsequently incorporated into the dolomite. This may help to explain the lack of calcite cementation despite the extensive skeletal aragonite dissolution.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1234341','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1234341"><span>Extracting uranium from <span class="hlt">seawater</span>: Promising AI series adsorbents</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Das, Sadananda; Oyola, Y.; Mayes, Richard T.</p> <p></p> <p>A series of adsorbent (AI10 through AI17) were successfully developed at ORNL by radiation induced graft polymerization (RIGP) of acrylonitrile (AN) and vinylphosphonic acid (VPA) (at different mole/mole ratios) onto high surface area polyethylene fiber, with higher degree of grafting which ranges from 110 300%. The grafted nitrile groups were converted to amidoxime groups by reaction with 10 wt% hydroxylamine at 80 C for 72 hours. The amidoximated adsorbents were then conditioned with 0.44M KOH at 80 C followed by screening at ORNL with simulated <span class="hlt">seawater</span> spiked with 8 ppm uranium. Uranium adsorption capacity in simulated <span class="hlt">seawater</span> screening ranged frommore » 171-187 g-U/kg-ads irrespective of %DOG. The performance of the adsorbents for uranium adsorption in natural <span class="hlt">seawater</span> was also carried out using flow-through-column at Pacific Northwest National Laboratory (PNNL). The three hours KOH conditioning was better for higher uranium uptake than one hour. The adsorbent AI11 containing AN and VPA at the mole ration of 3.52, emerged as the potential candidate for higher uranium adsorption (3.35 g-U/Kg-ads.) after 56 days of exposure in the <span class="hlt">seawater</span> in the flow-through-column. The rate vanadium adsorption over uranium was linearly increased throughout the 56 days exposure. The total vanadium uptake was ~5 times over uranium after 56 days.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012PhDT.......190H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012PhDT.......190H"><span>The influence of sea <span class="hlt">ice</span> on Antarctic <span class="hlt">ice</span> core sulfur chemistry and on the future evolution of Arctic snow depth: Investigations using global models</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hezel, Paul J.</p> <p></p> <p>Observational studies have examined the relationship between methanesulfonic acid (MSA) measured in Antarctic <span class="hlt">ice</span> cores and sea <span class="hlt">ice</span> extent measured by satellites with the aim of producing a proxy for past sea <span class="hlt">ice</span> extent. MSA is an oxidation product of dimethylsulfide (DMS) and is potentially linked to sea <span class="hlt">ice</span> based on observations of very high surface <span class="hlt">seawater</span> DMS in the sea <span class="hlt">ice</span> zone. Using a global chemical transport model, we present the first modeling study that specifically examines this relationship on interannual and on glacial-interglacial time scales. On interannual time scales, the model shows no robust relationship between MSA deposited in Antarctica and sea <span class="hlt">ice</span> extent. We show that lifetimes of MSA and DMS are longer in the high latitudes than in the global mean, interannual variability of sea <span class="hlt">ice</span> is small (<25%) as a fraction of sea <span class="hlt">ice</span> area, and sea <span class="hlt">ice</span> determines only a fraction of the variability (<30%) of DMS emissions from the ocean surface. A potentially larger fraction of the variability in DMS emissions is determined by surface wind speed (up to 46%) via the parameterization for ocean-to-atmosphere gas exchange. Furthermore, we find that a significant fraction (up to 74%) of MSA deposited in Antarctica originates from north of 60°S, north of the seasonal sea <span class="hlt">ice</span> zone. We then examine the deposition of MSA and non-sea-salt sulfate (nss SO2-4 ) on glacial-interglacial time scales. <span class="hlt">Ice</span> core observations on the East Antarctic Plateau suggest that MSA increases much more than nss SO2-4 during the last glacial maximum (LGM) compared to the modern period. It has been suggested that high MSA during the LGM is indicative of higher primary productivity and DMS emissions in the LGM compared to the modern day. Studies have also shown that MSA is subject to post-depositional volatilization, especially during the modern period. Using the same chemical transport model driven by meteorology from a global climate model, we examine the sensitivity of MSA and nss</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-PIA17281.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-PIA17281.html"><span><span class="hlt">Ice</span> Front at Venable <span class="hlt">Ice</span> Shelf</span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2013-06-13</p> <p>This photo, taken onboard the Chilean Navy P3 aircraft, shows the <span class="hlt">ice</span> front of Venable <span class="hlt">Ice</span> Shelf, West Antarctica, in October 2008. It is an example of a small-size <span class="hlt">ice</span> shelf that is a large melt water producer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015AGUFM.C21A0698B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015AGUFM.C21A0698B"><span>Looking Into and Through the Ross <span class="hlt">Ice</span> Shelf - ROSETTA-<span class="hlt">ICE</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bell, R. E.</p> <p>2015-12-01</p> <p>Our current understanding of the structure and stability of the Ross <span class="hlt">Ice</span> Shelf is based on satellite studies of the <span class="hlt">ice</span> surface and the 1970's RIGGS program. The study of the flowlines evident in the MODIS imagery combined with surface geophysics has revealed a complex history with <span class="hlt">ice</span> streams Mercer, Whillans and Kamb changing velocity over the past 1000 years. Here, we present preliminary <span class="hlt">Ice</span>Pod and <span class="hlt">Ice</span>Bridge radar data acquired in December 2014 and November 2013 across the Ross <span class="hlt">Ice</span> Shelf that show clearly, for the first time, the structure of the <span class="hlt">ice</span> shelf and provide insights into <span class="hlt">ice</span>-ocean interaction. The three major layers of the <span class="hlt">ice</span> shelf are (1) the continental meteoric <span class="hlt">ice</span> layer), <span class="hlt">ice</span> formed on the grounded <span class="hlt">ice</span> sheet that entered the <span class="hlt">ice</span> shelf where <span class="hlt">ice</span> streams and outlet glaciers crossed the grounding line (2) the locally accumulating meteoric <span class="hlt">ice</span> layer, <span class="hlt">ice</span> and snow that forms from snowfall on the floating <span class="hlt">ice</span> shelf and (3) a basal marine <span class="hlt">ice</span> layer. The locally accumulating meteoric <span class="hlt">ice</span> layer contains well-defined internal layers that are generally parallel to the <span class="hlt">ice</span> surface and thickens away from the grounding line and reaches a maximum thickness of 220m along the line crossing Roosevelt Island. The continental meteoric layer is located below a broad irregular internal reflector, and is characterized by irregular internal layers. These internal layers are often folded, likely a result of deformation as the <span class="hlt">ice</span> flowed across the grounding line. The basal marine <span class="hlt">ice</span> layer, up to 50m thick, is best resolved in locations where basal crevasses are present, and appears to thicken along the flow at rates of decimeters per year. Each individual flowband of the <span class="hlt">ice</span> shelf contains layers that are distinct in their structure. For example, the thickness of the locally accumulated layer is a function of both the time since crossing the grounding line and the thickness of the incoming <span class="hlt">ice</span>. Features in the meteoric <span class="hlt">ice</span>, such as distinct folds, can be traced between</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C42A..05C','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C42A..05C"><span><span class="hlt">Ice</span> shelf melt rates in Greenland and Antarctica using time-tagged digital imagery from World View and TanDEM-X</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Charolais, A.; Rignot, E. J.; Milillo, P.; Scheuchl, B.; Mouginot, J.</p> <p>2017-12-01</p> <p>The floating extensions of glaciers, or <span class="hlt">ice</span> shelves, melt vigorously in contact with ocean waters. Melt is non uniform, with the highest melt taking place in the deepest part of the cavity, where thermal forcing is the greatest because of 1) the pressure dependence of the freezing point of the <span class="hlt">seawater/ice</span> mixture and 2) subglacial water injects fresh, buoyant, cold melt water to fuel stronger <span class="hlt">ice</span>-ocean interactions. Melt also forms along preferential channels, which are not stationary, and create lines of weakness in the shelf. <span class="hlt">Ice</span> shelf melt rates have been successfully measured from space over the entire Antarctic continent and on the <span class="hlt">ice</span> shelves in Greenland using an Eulerian approach that combines <span class="hlt">ice</span> thickness, <span class="hlt">ice</span> velocity vectors, surface mass balance data, and measurements of <span class="hlt">ice</span> thinning rates. The Eulerian approach is limited by the precision of the thickness gradients, typically of a few km, and requires significant spatial averaging to remove advection effects. A Lagrangian approach has been shown to be robust to advection effects and provides higher resolution details. We implemented a Lagrangian methodology for time-tagged World View DEMs by the Polar Geoscience Center (PGS) at the University of Minnesota and time-tagged TanDEM-X DEMs separated by one year. We derive melt rates on a 300-m grid with a precision of a few m/yr. Melt is strongest along grounding lines and along preferred channels. Channels are non-stationary because melt is not the same on opposite sides of the channels. Examining time series of data and comparing with the time-dependent grounding line positions inferred from satellite radar interferometry, we evaluate the magnitude of melt near the grounding line and even within the grounding zone. A non-zero melt rate in the grounding zone has vast implications for <span class="hlt">ice</span> sheet modeling. This work is funded by a grant from NASA Cryosphere Program.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70025480','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70025480"><span>Uptake of elements from <span class="hlt">seawater</span> by ferromanganese crusts: Solid-phase associations and <span class="hlt">seawater</span> speciation</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Koschinsky, A.; Hein, J.R.</p> <p>2003-01-01</p> <p>Marine Fe-Mn oxyhydroxide crusts form by precipitation of dissolved components from <span class="hlt">seawater</span>. Three hydrogenetic crust samples (one phosphatized) and two hydrothermal Mn-oxide samples were subjected to a sequential-leaching procedure in order to determine the host phases of 40 elements. Those host-phase associations are discussed with respect to element speciation in <span class="hlt">seawater</span>. The partitioning of elements between the two major phases, Mn oxide and Fe oxyhydroxide, can in a first-order approximation be explained by a simple sorption model related to the inorganic speciation of the elements in <span class="hlt">seawater</span>, as has been proposed in earlier models. Free and weakly complexed cations, such as alkali and alkaline earth metals, Mn, Co, Ni, Zn, T1(I), and partly Y, are sorbed preferentially on the negatively charged surface of the MnO2 in hydrogenetic crusts. The driving force is a strong coulombic interaction. All neutral or negatively charged chloro (Cd, Hg, T1), carbonate (Cu, Y, Pb, and U), and hydroxide (Be, Sc, Ti, Fe, Zr, Nb, In, Sn, Sb, Te, Hf, Ta, Bi, Th, and T1(III)) complexes and oxyanions (V, Cr, As, Se, Mo, and W) bind to the slightly positively charged surface of the amorphous FeOOH phase. While coulombic interaction can explain the sorption of the negatively charged species, the binding of neutral species is based on specific chemical interaction. Organic complexation of elements in deep-ocean water seems to be at most of minor importance. Surface oxidation can explain some strong metal associations, e.g. of Co and T1 with the MnO2 and Te with the FeOOH. Sorption reactions initially driven by coulombic forces are often followed by the formation of specific bonds between the adsorbate and the atoms of the oxide surface. Differences in the associations of some metals between the non-phosphatized and phosphatized hydrogenetic crusts and between the hydrogenetic and the hydrothermal samples reflect the different physico-chemical environments of formation and</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUFM.C21D..08R','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUFM.C21D..08R"><span>Extensive massive basal-<span class="hlt">ice</span> structures in West Antarctica relate to <span class="hlt">ice</span>-sheet anisotropy and <span class="hlt">ice</span>-flow</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Ross, N.; Bingham, R. G.; Corr, H. F. J.; Siegert, M. J.</p> <p>2016-12-01</p> <p>Complex structures identified within both the East Antarctic and Greenland <span class="hlt">ice</span> sheets are thought to be generated by the action of basal water freezing to the <span class="hlt">ice</span>-sheet base, evolving under <span class="hlt">ice</span> flow. Here, we use <span class="hlt">ice</span>-penetrating radar to image an extensive series of similarly complex basal <span class="hlt">ice</span> facies in West Antarctica, revealing a thick (>500 m) tectonised unit in an area of cold-based and relatively slow-flowing <span class="hlt">ice</span>. We show that major folding and overturning of the unit perpendicular to <span class="hlt">ice</span> flow elevates deep, warm <span class="hlt">ice</span> into the mid <span class="hlt">ice</span>-sheet column. Fold axes align with present <span class="hlt">ice</span> flow, and axis amplitudes increase down-<span class="hlt">ice</span>, suggesting long-term consistency in the direction and convergence of flow. In the absence of basal water, and the draping of the tectonised unit over major subglacial mountain ranges, the formation of the unit must be solely through the deformation of meteoric <span class="hlt">ice</span>. Internal layer radar reflectivity is consistently greater parallel to flow compared with the perpendicular direction, revealing <span class="hlt">ice</span>-sheet crystal anisotropy is associated with the folding. By linking layers to the Byrd <span class="hlt">ice</span>-core site, we show the basal <span class="hlt">ice</span> dates to at least the last glacial cycle and may be as old as the last interglacial. Deformation of deep-<span class="hlt">ice</span> in this sector of WAIS, and potentially elsewhere in Antarctica, may be caused by differential shearing at interglacial-glacial boundaries, in a process analogous to that proposed for interior Greenland. The scale and heterogeneity of the englacial structures, and their subsequent impact on <span class="hlt">ice</span> sheet rheology, means that the nature of <span class="hlt">ice</span> flow across the bulk of West Antarctica must be far more complex that is currently accounted for by any numerical <span class="hlt">ice</span> sheet model.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOS.A24C2604S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOS.A24C2604S"><span>Atmospheric Aerosol Emissions Related to the Mediterranean <span class="hlt">Seawater</span> Biogeochemistry</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sellegri, K.; Schwier, A.; Rose, C.; Gazeau, F. P. H.; Guieu, C.; D'anna, B.; Ebling, A. M.; Pey, J.; Marchand, N.; Charriere, B.; Sempéré, R.; Mas, S.</p> <p>2016-02-01</p> <p>Marine aerosols contribute significantly to the global aerosol load and consequently has an important impact on the Earth's climate. Different factors influence the way they are produced at the air/<span class="hlt">seawater</span> interface. The sea state (whitecap coverage, temperature, etc. ) influence the size and concentration of primarily produced particles but also biogeochemical characteristics of the <span class="hlt">seawater</span> influence both the physical and chemical primary fluxes to the atmosphere. An additional aerosol source of marine aerosol to the atmosphere is the formation of new particles by gaz-to-particle conversion, i.e. nucleation. How the <span class="hlt">seawater</span> and surface microlayer biogeochemical compositions influences the aerosol emissions is still a large debate. In order to study marine emissions, one approach is to use semi-controlled environments such as mesocosms. Within the MedSea and SAM projects, we characterize the primary Sea Spray Aerosol (SSA) during mesocosms experiments performed during different seasons in the Mediteranean Sea. Mesocosms were either left unchanged as control or enriched by addition of nutriments in order to create different levels of phytoplanctonic activities. The mesocosms waters were daily analyzed for their chemical and biological composition (DOC, CDOM, TEP, Chl-a, virus, bacteria, phytoplankton and zooplankton concentrations). SSA production by bubble bursting was daily simulated in a dedicated set-up. The size segregated SSA number fluxes, cloud condensation nuclei (CCN) properties, and chemical composition were determined as a function of the <span class="hlt">seawater</span> characteristics. We show that the SSA organic content was clearly correlated to the <span class="hlt">seawater</span> Chl-a level, provided that the mesocosm was not enriched to create an artificial phytoplanctonic bloom. In our experiments, the enrichment of the <span class="hlt">seawater</span> with natural surface microlayer did not impact the SSA organic content nor its CCN properties. At last, nucleation of secondary particles were observed to occur in</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-PIA13420.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-PIA13420.html"><span>Proposed Perrier Ocean for Enceladus</span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2010-10-04</p> <p>A graphic laid atop an image of Enceladus jets taken by NASA Cassini imaging cameras shows bubbles in <span class="hlt">seawater</span> traveling through a passage in the <span class="hlt">ice</span> crust to feed a geyser. <span class="hlt">Seawater</span> flows back down to the subsurface ocean through cracks in the <span class="hlt">ice</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1221496-macroporous-monoliths-trace-metal-extraction-from-seawater','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1221496-macroporous-monoliths-trace-metal-extraction-from-seawater"><span>Macroporous monoliths for trace metal extraction from <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Yue, Yanfeng; Mayes, Richard; Gill, Gary A.</p> <p>2015-05-29</p> <p>The viability of <span class="hlt">seawater</span>-based uranium recovery depends on the uranium adsorption rate and capacity, since the concentration of uranium in the oceans is relatively low (3.3 μgL⁻¹). An important consideration for a fast adsorption is to maximize the adsorption properties of adsorbents such as surface areas and pore structures, which can greatly improve the kinetics of uranium extraction and the adsorption capacity simultaneously. Following this consideration, macroporous monolith adsorbents were prepared from the copolymerization of acrylonitrile (AN) and N, N’-methylenebis(acrylamide) (MBAAm) based on a cryogel method using both hydrophobic and hydrophilic monomers. The monolithic sorbents were tested with simulated seawatermore » containing a high uranyl concentration (–6 ppm) and the uranium adsorption results showed that the adsorption capacities are strongly influenced by the ratio of monomer to the crosslinker, i.e., the density of the amidoxime groups. The preliminary <span class="hlt">seawater</span> testing indicates the high salinity content of <span class="hlt">seawater</span> does not hinder the adsorption of uranium.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015CRGeo.347..368S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015CRGeo.347..368S"><span>The mercury isotope composition of Arctic coastal <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Štrok, Marko; Baya, Pascale Anabelle; Hintelmann, Holger</p> <p>2015-11-01</p> <p>For the first time, Hg isotope composition of <span class="hlt">seawater</span> in the Canadian Arctic Archipelago is reported. Hg was pre-concentrated from large volumes of <span class="hlt">seawater</span> sampling using anion exchange resins onboard the research vessel immediately after collection. Elution of Hg was performed in laboratory followed by isotope composition determination by multi-collector inductively coupled plasma mass spectrometry (MC-ICP-MS). For comparison, <span class="hlt">seawater</span> from two stations was shipped to the laboratory and processed within it. Results showed negative mass-dependent fractionation in the range from -2.85 to -1.10‰ for δ202Hg, as well as slightly positive mass-independent fractionation of odd Hg isotopes. Positive mass-independent fractionation of 200Hg was also observed. Samples that were pre-concentrated in the laboratory showed different Hg isotope signatures and this is most probably due to the abiotic reduction of Hg in the dark by organic matter during storage and shipment after sampling. This emphasizes the need for immediate onboard pre-concentration.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_17");'>17</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li class="active"><span>19</span></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_19 --> <div id="page_20" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="381"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2555217','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2555217"><span>Dichlorvos <span class="hlt">vapour</span> disinsection of aircraft</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Jensen, Jens A.; Flury, Vincent P.; Schoof, Herbert F.</p> <p>1965-01-01</p> <p>The authors describe the testing of an automatic aircraft disinsection system permanently installed on a commercial DC-6B passenger aircraft. An air-compressor forces ambient cabin air, partially saturated with dichlorvos <span class="hlt">vapour</span> at a set concentration, through the cabin, cockpit and baggage compartments of the aircraft for 30 minutes. Insecticide concentrations and insect mortality were observed in post-overhaul check flights, and insect mortality and passenger reactions were observed on scheduled flights between Miami, Florida, and Nassau, Bahamas. The results showed satisfactory biological efficiency. The passengers were unaware of the disinsection process and showed no signs of discomfort. ImagesFIG. 1FIG. 2FIG. 3 PMID:14310904</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28775362','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28775362"><span>Oscillatory <span class="hlt">vapour</span> shielding of liquid metal walls in nuclear fusion devices.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>van Eden, G G; Kvon, V; van de Sanden, M C M; Morgan, T W</p> <p>2017-08-04</p> <p>Providing an efficacious plasma facing surface between the extreme plasma heat exhaust and the structural materials of nuclear fusion devices is a major challenge on the road to electricity production by fusion power plants. The performance of solid plasma facing surfaces may become critically reduced over time due to progressing damage accumulation. Liquid metals, however, are now gaining interest in solving the challenge of extreme heat flux hitting the reactor walls. A key advantage of liquid metals is the use of <span class="hlt">vapour</span> shielding to reduce the plasma exhaust. Here we demonstrate that this phenomenon is oscillatory by nature. The dynamics of a Sn <span class="hlt">vapour</span> cloud are investigated by exposing liquid Sn targets to H and He plasmas at heat fluxes greater than 5 MW m -2 . The observations indicate the presence of a dynamic equilibrium between the plasma and liquid target ruled by recombinatory processes in the plasma, leading to an approximately stable surface temperature.<span class="hlt">Vapour</span> shielding is one of the interesting mechanisms for reducing the heat load to plasma facing components in fusion reactors. Here the authors report on the observation of a dynamic equilibrium between the plasma and the divertor liquid Sn surface leading to an overall stable surface temperature.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/23357868','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/23357868"><span>Oxidation of volatile organic <span class="hlt">vapours</span> in air by solid potassium permanganate.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Mahmoodlu, Mojtaba Ghareh; Hartog, Niels; Majid Hassanizadeh, S; Raoof, Amir</p> <p>2013-06-01</p> <p>Volatile organic compounds (VOCs) may frequently contaminate groundwater and pose threat to human health when migrating into the unsaturated soil zone and upward to the indoor air. The kinetic of chemical oxidation has been investigated widely for dissolved VOCs in the saturated zone. But, so far there have been few studies on the use of in situ chemical oxidation (ISCO) of <span class="hlt">vapour</span> phase contaminants. In this study, batch experiments were carried out to evaluate the oxidation of trichloroethylene (TCE), ethanol, and toluene <span class="hlt">vapours</span> by solid potassium permanganate. Results revealed that solid potassium permanganate is able to transform the <span class="hlt">vapour</span> of these compounds into harmless oxidation products. The degradation rates for TCE and ethanol were higher than for toluene. The degradation process was modelled using a kinetic model, linear in the gas concentration of VOC [ML(-3)] and relative surface area of potassium permanganate grains (surface area of potassium permanganate divided by gas volume) [L(-1)]. The second-order reaction rate constants for TCE, ethanol, and toluene were found to be equal to 2.0×10(-6) cm s(-1), 1.7×10(-7) cm s(-1), and 7.0×10(-8) cm s(-1), respectively. Copyright © 2013 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26167727','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26167727"><span>Degradation Products of Benzophenone-3 in Chlorinated <span class="hlt">Seawater</span> Swimming Pools.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Manasfi, Tarek; Storck, Veronika; Ravier, Sylvain; Demelas, Carine; Coulomb, Bruno; Boudenne, Jean-Luc</p> <p>2015-08-04</p> <p>Oxybenzone (2-hydroxy-4-methoxyphenone, benzophenone-3) is one of the UV filters commonly found in sunscreens. Its presence in swimming pools and its reactivity with chlorine has already been demonstrated but never in <span class="hlt">seawater</span> swimming pools. In these pools, chlorine added for disinfection results in the formation of bromine, due to the high levels of bromide in <span class="hlt">seawater</span>, and leads to the formation of brominated disinfection byproducts, known to be more toxic than chlorinated ones. Therefore, it seems important to determine the transformation products of oxybenzone in chlorinated <span class="hlt">seawater</span> swimming pools; especially that users of <span class="hlt">seawater</span> swimming pools may apply sunscreens and other personal-care products containing oxybenzone before going to pools. This leads to the introduction of oxybenzone to pools, where it reacts with bromine. For this purpose, the reactivity of oxybenzone has been examined as a function of chlorine dose and temperature in artificial <span class="hlt">seawater</span> to assess its potential to produce trihalomethanes and to determine the byproducts generated following chlorination. Increasing doses of chlorine and increasing temperatures enhanced the formation of bromoform. Experiments carried out with excess doses of chlorine resulted in the degradation of oxybenzone and allowed the determination of the degradation mechanisms leading to the formation of bromoform. In total, ten transformation products were identified, based on which the transformation pathway was proposed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2005JNuM..345...96P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2005JNuM..345...96P"><span><span class="hlt">Vapour</span> pressure and standard enthalpy of sublimation of KBF 4 by a TG based transpiration technique</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pankajavalli, R.; Ananthasivan, K.; Anthonysamy, S.; Vasudeva Rao, P. R.</p> <p>2005-10-01</p> <p>A horizontal thermobalance was adapted as a transpiration apparatus for the measurement of the <span class="hlt">vapour</span> pressure of KBF4 (s). Attainment of equilibrium was ascertained by the invariance of the measured values of the <span class="hlt">vapour</span> pressures over a range of flows under isothermal conditions. Measured values of the <span class="hlt">vapour</span> pressures could be represented by the least-squares expressions: log (p/Pa) = 8.16(±0.01) - 4892(±248)/T(K)(538-560 K), log (p/Pa) = 6.85(±0.06) - 4158(±240)/T(K) (576-660 K), which correspond to the equilibria of orthorhombic and cubic KBF4 <span class="hlt">vapours</span>, respectively. From these expressions the temperature of transformation of the orthorhombic to the cubic phase was identified to be 561 K. From the slopes of the above equations, the enthalpies of sublimation of the orthorhombic and cubic phases were found to be (93.7 ± 4.7) and (79.6 ± 4.6) kJ mol-1, respectively. These values differ by 14.1 kJ mol-1 which could be ascribed to the enthalpy of the orthorhombic to cubic phase transition of KBF4. Third-law analysis of the <span class="hlt">vapour</span> pressure data yielded a value of (104.6 ± 1.0) kJ mol-1 for Δ Hsubo of KBF4 (s) at 298.15 K.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16470625','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16470625"><span>Micellar electrokinetic chromatography and capillary electrochromatography of nitroaromatic explosives in <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Giordano, Braden C; Copper, Christine L; Collins, Greg E</p> <p>2006-02-01</p> <p>The ability to separate nitroaromatic and nitramine explosives in <span class="hlt">seawater</span> sample matrices is demonstrated using both MEKC and CEC. While several capillary-based separations exist for explosives, none address direct sampling from <span class="hlt">seawater</span>, a sample matrix of particular interest in the detection of undersea mines. Direct comparisons are made between MEKC and CEC in terms of sensitivity and separation efficiency for the analysis of 14 explosives and explosive degradation products in <span class="hlt">seawater</span> and diluted <span class="hlt">seawater</span>. The use of high-salt stacking with MEKC results, on average, in a three-fold increase in the number of theoretical plates, and nearly double resolution for samples prepared in 25% <span class="hlt">seawater</span>. By taking advantage of long injection times in conjunction with stacking, detection limits down to sub mg/L levels are attainable; however, resolution is sacrificed. CEC of explosive mixtures using sol-gels prepared from methyltrimethoxysilane does not perform as well as MEKC in terms of resolving power, but does permit extended injection times for concentrating analyte onto the head of the separation column with little or no subsequent loss in resolution. Electrokinetic injections of 8 min at high voltage allow for detection limits of explosives below 100 microg/L.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28911489','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28911489"><span>Effects of electrode settings on chlorine generation efficiency of electrolyzing <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hsu, Guoo-Shyng Wang; Hsia, Chih-Wei; Hsu, Shun-Yao</p> <p>2015-12-01</p> <p>Electrolyzed water has significant disinfection effects, can comply with food safety regulations, and is environmental friendly. We investigated the effects of immersion depth of electrodes, stirring, electrode size, and electrode gap on the properties and chlorine generation efficiency of electrolyzing <span class="hlt">seawater</span> and its storage stability. Results indicated that temperature and oxidation-reduction potential (ORP) of the <span class="hlt">seawater</span> increased gradually, whereas electrical conductivity decreased steadily in electrolysis. During the electrolysis process, pH values and electric currents also decreased slightly within small ranges. Additional stirring or immersing the electrodes deep under the <span class="hlt">seawater</span> significantly increased current density without affecting its electric efficiency and current efficiency. Decreasing electrode size or increasing electrode gap decreased chlorine production and electric current of the process without affecting its electric efficiency and current efficiency. Less than 35% of chlorine in the electrolyzed <span class="hlt">seawater</span> was lost in a 3-week storage period. The decrement trend leveled off after the 1 st week of storage. The electrolyzing system is a convenient and economical method for producing high-chlorine <span class="hlt">seawater</span>, which will have high potential applications in agriculture, aquaculture, or food processing. Copyright © 2015. Published by Elsevier B.V.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4759657','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4759657"><span>Metrological challenges for measurements of key climatological observables: Oceanic salinity and pH, and atmospheric humidity. Part 1: Overview</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Feistel, R; Wielgosz, R; Bell, S A; Camões, M F; Cooper, J R; Dexter, P; Dickson, A G; Fisicaro, P; Harvey, A H; Heinonen, M; Hellmuth, O; Kretzschmar, H-J; Lovell-Smith, J W; McDougall, T J; Pawlowicz, R; Ridout, P; Seitz, S; Spitzer, P; Stoica, D; Wolf, H</p> <p>2016-01-01</p> <p>Water in its three ambient phases plays the central thermodynamic role in the terrestrial climate system. Clouds control Earth’s radiation balance, atmospheric water <span class="hlt">vapour</span> is the strongest “greenhouse” gas, and non-equilibrium relative humidity at the air-sea interface drives evaporation and latent heat export from the ocean. On climatic time scales, melting <span class="hlt">ice</span> caps and regional deviations of the hydrological cycle result in changes of <span class="hlt">seawater</span> salinity, which in turn may modify the global circulation of the oceans and their ability to store heat and to buffer anthropogenically produced carbon dioxide. In this paper, together with three companion articles, we examine the climatologically relevant quantities ocean salinity, <span class="hlt">seawater</span> pH and atmospheric relative humidity, noting fundamental deficiencies in the definitions of those key observables, and their lack of secure foundation on the International System of Units, the SI. The metrological histories of those three quantities are reviewed, problems with their current definitions and measurement practices are analysed, and options for future improvements are discussed in conjunction with the recent <span class="hlt">seawater</span> standard TEOS-10. It is concluded that the International Bureau of Weights and Measures, BIPM, in cooperation with the International Association for the Properties of Water and Steam, IAPWS, along with other international organisations and institutions, can make significant contributions by developing and recommending state-of-the-art solutions for these long standing metrological problems in climatology. PMID:26900179</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20150002346','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20150002346"><span><span class="hlt">Ice</span> Roughness in Short Duration SLD <span class="hlt">Icing</span> Events</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>McClain, Stephen T.; Reed, Dana; Vargas, Mario; Kreeger, Richard E.; Tsao, Jen-Ching</p> <p>2014-01-01</p> <p><span class="hlt">Ice</span> accretion codes depend on models of roughness parameters to account for the enhanced heat transfer during the <span class="hlt">ice</span> accretion process. While mitigating supercooled large droplet (SLD or Appendix O) <span class="hlt">icing</span> is a significant concern for manufacturers seeking future vehicle certification due to the pending regulation, historical <span class="hlt">ice</span> roughness studies have been performed using Appendix C <span class="hlt">icing</span> clouds which exhibit mean volumetric diameters (MVD) much smaller than SLD clouds. Further, the historical studies of roughness focused on extracting parametric representations of <span class="hlt">ice</span> roughness using multiple images of roughness elements. In this study, the <span class="hlt">ice</span> roughness developed on a 21-in. NACA 0012 at 0deg angle of attack exposed to short duration SLD <span class="hlt">icing</span> events was measured in the <span class="hlt">Icing</span> Research Tunnel at the NASA Glenn Research Center. The MVD's used in the study ranged from 100 micrometer to 200 micrometers, in a 67 m/s flow, with liquid water contents of either 0.6 gm/cubic meters or 0.75 gm/cubic meters. The <span class="hlt">ice</span> surfaces were measured using a Romer Absolute Arm laser scanning system. The roughness associated with each surface point cloud was measured using the two-dimensional self-organizing map approach developed by McClain and Kreeger (2013) resulting in statistical descriptions of the <span class="hlt">ice</span> roughness.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017PhFl...29g4102P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017PhFl...29g4102P"><span>Combustion dynamics of low <span class="hlt">vapour</span> pressure nanofuel droplets</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Pandey, Khushboo; Chattopadhyay, Kamanio; Basu, Saptarshi</p> <p>2017-07-01</p> <p>Multiscale combustion dynamics, shape oscillations, secondary atomization, and precipitate formation have been elucidated for low <span class="hlt">vapour</span> pressure nanofuel [n-dodecane seeded with alumina nanoparticles (NPs)] droplets. Dilute nanoparticle loading rates (0.1%-1%) have been considered. Contrary to our previous studies of ethanol-water blend (high <span class="hlt">vapour</span> pressure fuel), pure dodecane droplets do not exhibit internal boiling after ignition. However, variation in surface tension due to temperature causes shape deformations for pure dodecane droplets. In the case of nanofuels, intense heat release from the enveloping flame leads to the formation of micron-size aggregates (of alumina NPS) which serve as nucleation sites promoting heterogeneous boiling. Three boiling regimes (A, B, and C) have been identified with varying bubble dynamics. We have deciphered key mechanisms responsible for the growth, transport, and rupture of the bubbles. Bubble rupture causes ejections of liquid droplets termed as secondary atomization. Ejection of small bubbles (mode 1) resembles the classical <span class="hlt">vapour</span> bubble collapse mechanism near a flat free surface. However, large bubbles induce severe shape deformations as well as bulk oscillations. Rupture of large bubbles results in high speed liquid jet formation which undergoes Rayleigh-Plateau tip break-up. Both modes contribute towards direct fuel transfer from the droplet surface to flame envelope bypassing diffusion limitations. Combustion lifetime of nanofuel droplets consequently has two stages: stage I (where bubble dynamics are dominant) and stage II (formation of gelatinous mass due to continuous fuel depletion; NP agglomeration). In the present work, variation of flame dynamics and spatio-temporal heat release (HR) have been analysed using high speed OH* chemiluminescence imaging. Fluctuations in droplet shape and flame heat release are found to be well correlated. Droplet flame is bifurcated in two zones (I and II). Flame response is</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29610528','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29610528"><span>Highly efficient solar <span class="hlt">vapour</span> generation via hierarchically nanostructured gels.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Zhao, Fei; Zhou, Xingyi; Shi, Ye; Qian, Xin; Alexander, Megan; Zhao, Xinpeng; Mendez, Samantha; Yang, Ronggui; Qu, Liangti; Yu, Guihua</p> <p>2018-04-02</p> <p>Solar <span class="hlt">vapour</span> generation is an efficient way of harvesting solar energy for the purification of polluted or saline water. However, water evaporation suffers from either inefficient utilization of solar energy or relies on complex and expensive light-concentration accessories. Here, we demonstrate a hierarchically nanostructured gel (HNG) based on polyvinyl alcohol (PVA) and polypyrrole (PPy) that serves as an independent solar <span class="hlt">vapour</span> generator. The converted energy can be utilized in situ to power the vaporization of water contained in the molecular meshes of the PVA network, where water evaporation is facilitated by the skeleton of the hydrogel. A floating HNG sample evaporated water with a record high rate of 3.2 kg m -2  h -1 via 94% solar energy from 1 sun irradiation, and 18-23 litres of water per square metre of HNG was delivered daily when purifying brine water. These values were achievable due to the reduced latent heat of water evaporation in the molecular mesh under natural sunlight.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018NatNa..13..489Z','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018NatNa..13..489Z"><span>Highly efficient solar <span class="hlt">vapour</span> generation via hierarchically nanostructured gels</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Zhao, Fei; Zhou, Xingyi; Shi, Ye; Qian, Xin; Alexander, Megan; Zhao, Xinpeng; Mendez, Samantha; Yang, Ronggui; Qu, Liangti; Yu, Guihua</p> <p>2018-06-01</p> <p>Solar <span class="hlt">vapour</span> generation is an efficient way of harvesting solar energy for the purification of polluted or saline water. However, water evaporation suffers from either inefficient utilization of solar energy or relies on complex and expensive light-concentration accessories. Here, we demonstrate a hierarchically nanostructured gel (HNG) based on polyvinyl alcohol (PVA) and polypyrrole (PPy) that serves as an independent solar <span class="hlt">vapour</span> generator. The converted energy can be utilized in situ to power the vaporization of water contained in the molecular meshes of the PVA network, where water evaporation is facilitated by the skeleton of the hydrogel. A floating HNG sample evaporated water with a record high rate of 3.2 kg m-2 h-1 via 94% solar energy from 1 sun irradiation, and 18-23 litres of water per square metre of HNG was delivered daily when purifying brine water. These values were achievable due to the reduced latent heat of water evaporation in the molecular mesh under natural sunlight.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015ApCM...22..693Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015ApCM...22..693Y"><span>Long-Term Viscoelastic Response of E-glass/Bismaleimide Composite in <span class="hlt">Seawater</span> Environment</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yian, Zhao; Zhiying, Wang; Keey, Seah Leong; Boay, Chai Gin</p> <p>2015-12-01</p> <p>The effect of <span class="hlt">seawater</span> absorption on the long-term viscoelastic response of E-glass/BMI composite is presented in this paper. The diffusion of <span class="hlt">seawater</span> into the composite shows a two-stage behavior, dominated by Fickian diffusion initially and followed by polymeric relaxation. The Glass transition temperature (Tg) of the composite with <span class="hlt">seawater</span> absorption is considerably lowered due to the plasticization effect. However the effect of water absorption at 50 °C is found to be reversible after drying process. The time-temperature superposition (TTS) was performed based on the results of Dynamic Mechanical Analysis to construct the master curve of storage modulus. The shift factors exhibit Arrhenius behavior when temperature is well below Tg and Vogel-Fulcher-Tammann (VFT) like behavior when temperature gets close to glass transition region. As a result, a semi-empirical formulation is proposed to account for the <span class="hlt">seawater</span> absorption effect in predicting long-term viscoelastic response of BMI composites based on temperature dependent storage modulus and TTS. The predicted master curves show that the degradation of storage modulus accelerates with both <span class="hlt">seawater</span> exposure and increasing temperature. The proposed formulation can be applied to predict the long-term durability of any thermorheologically simple composite materials in <span class="hlt">seawater</span> environment.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=183113','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=183113"><span>Occurrence of tributyltin-tolerant bacteria in tributyltin- or cadmium-containing <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Suzuki, S; Fukagawa, T; Takama, K</p> <p>1992-01-01</p> <p>Tributyltin chloride (TBTCl)-tolerant bacteria accounted for 90% of the flora in natural <span class="hlt">seawater</span> to which TBTCl was added. These tolerant bacteria were insensitive to 250 nmol of TBTCl per disc, and all were Vibrio species. Total counts of viable bacteria did not decrease upon storage of the TBTCl-treated <span class="hlt">seawater</span>, indicating that enrichment of tolerant strains took place. Addition of CdSO4 to <span class="hlt">seawater</span> resulted in the occurrence of TBTCl-tolerant bacteria as well as Cd-tolerant bacteria, suggesting some correlation of Cd tolerance and TBTCl tolerance. PMID:1444375</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013AGUFM.P53A1844S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013AGUFM.P53A1844S"><span>Design of an Autonomous Underwater Vehicle to Calibrate the Europa Clipper <span class="hlt">Ice</span>-Penetrating Radar</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stone, W.; Siegel, V.; Kimball, P.; Richmond, K.; Flesher, C.; Hogan, B.; Lelievre, S.</p> <p>2013-12-01</p> <p>Jupiter's moon Europa has been prioritized as the target for the Europa Clipper flyby mission. A key science objective for the mission is to remotely characterize the <span class="hlt">ice</span> shell and any subsurface water, including their heterogeneity, and the nature of surface-<span class="hlt">ice</span>-ocean exchange. This objective is a critical component of the mission's overarching goal of assessing the habitability of Europa. The instrument targeted for addressing key aspects of this goal is an <span class="hlt">ice</span>-penetrating radar (IPR). As a primary goal of our work, we will tightly couple airborne IPR studies of the Ross <span class="hlt">Ice</span> Shelf by the Europa Clipper radar team with ground-truth data to be obtained from sub-glacial sonar and bio-geochemical mapping of the corresponding <span class="hlt">ice</span>-water and water-rock interfaces using an advanced autonomous underwater vehicle (AUV). The ARTEMIS vehicle - a heavily morphed long-range, low drag variant of the highly successful 4-degree-of-freedom hovering sub-<span class="hlt">ice</span> ENDURANCE bot -- will be deployed from a sea-<span class="hlt">ice</span> drill hole adjacent the McMurdo <span class="hlt">Ice</span> Shelf (MIS) and will perform three classes of missions. The first includes original exploration and high definition mapping of both the <span class="hlt">ice</span>-water interface and the benthic interface on a length scale (approximately 10 kilometers under-<span class="hlt">ice</span> penetration radius) that will definitively tie it to the synchronous airborne IPR over-flights. These exploration and mapping missions will be conducted at up to 10 different locations along the MIS in order to capture varying <span class="hlt">ice</span> thickness and <span class="hlt">seawater</span> intrusion into the <span class="hlt">ice</span> shelf. Following initial mapping characterization, the vehicle will conduct astrobiology-relevant proximity operations using bio-assay sensors (custom-designed UV fluorescence and machine-vision-processed optical imagery) followed by point-targeted studies at regions of interest. Sample returns from the <span class="hlt">ice</span>-water interface will be triggered autonomously using real-time-processed instrument data and onboard decision-to-collect algorithms</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1361344-uranium-extraction-fuel-from-seawater','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1361344-uranium-extraction-fuel-from-seawater"><span>Uranium extraction: Fuel from <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Tsouris, Costas; Oak Ridge National Lab.</p> <p>2017-02-17</p> <p>Over four billion tonnes of uranium are currently in the oceans that could be harvested for nuclear fuel, but current capture methods have limited performance and reusability. Now, an electrochemical method using modified carbon electrodes is shown to be promising for the extraction of uranium from <span class="hlt">seawater</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1980JGR....85.1137W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1980JGR....85.1137W"><span>Crystal alignments in the Fast <span class="hlt">ice</span> of arctic Alaska</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Weeks, W. F.; Gow, A. J.</p> <p>1980-02-01</p> <p> alignments are believed to be the result of geometric selection, with the most favored orientation being that in which the current flows normal to the (0001) plates of <span class="hlt">ice</span> that comprise the dendritic sea <span class="hlt">ice/seawater</span> interface. The instantaneous current observations suggest SW nearshore currents along the Chukchi coast between SW of Point Lay and SW of the Rogers-Post Monument. In the vicinity of Barrow all currents measured along the Chukchi coast were toward the NE. Current directions along the Beaufort coast in the nearshore region were generally parallel to the coast, with 45% of the observations indicating currents toward the E and 55% currents toward the W.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/AD1013732','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/AD1013732"><span>Wave-<span class="hlt">Ice</span> and Air-<span class="hlt">Ice</span>-Ocean Interaction During the Chukchi Sea <span class="hlt">Ice</span> Edge Advance</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2015-09-30</p> <p>1 DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited. Wave -<span class="hlt">Ice</span> and Air-<span class="hlt">Ice</span>-Ocean Interaction During the...Chukchi Sea in the late summer have potentially changed the impact of fall storms by creating wave fields in the vicinity of the advancing <span class="hlt">ice</span> edge. A...first) wave -<span class="hlt">ice</span> interaction field experiment that adequately documents the relationship of a growing pancake <span class="hlt">ice</span> cover with a time and space varying</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70170486','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70170486"><span>Survival of the North American strain of viral hemorrhagic septicemia virus (VHSV) in filtered <span class="hlt">seawater</span> and <span class="hlt">seawater</span> containing ovarian fluid, crude oil and serum-enriched culture medium</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Kocan, R.M.; Hershberger, P.K.; Elder, N.E.</p> <p>2001-01-01</p> <p> The North American strain of viral hemorrhagic septicemia virus (NA-VHSV) could be recovered for up to 40 h in natural filtered <span class="hlt">seawater</span> (27 ppt) with a 50% loss of infectivity after approximately 10 h at 15°C. Addition of 10 ppb North Slope crude oil to the <span class="hlt">seawater</span> had no effect on virus survival. However, when various concentrations of teleost ovarian fluid were added to <span class="hlt">seawater</span>, virus could be recovered after 72 h at 0.01% ovarian fluid and after 96 h at 1.0%. When cell culture medium supplemented with 10% fetal bovine serum was added to the <span class="hlt">seawater</span>, 100% of the virus could be recovered for the first 15 d and 60% of the virus remained after 36 d. These findings quantify NA-VHSV infectivity in natural <span class="hlt">seawater</span> and demonstrate that ovarian fluid, which occurs naturally during spawning events, significantly prolongs the survival and infectivity of the virus. The extended stabilization of virus in culture medium supplemented with serum allows for low titer field samples to be collected and transported in an unfrozen state without significant loss of virus titer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19990071137&hterms=ice+mechanics&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D20%26Ntt%3Dice%2Bmechanics','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19990071137&hterms=ice+mechanics&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D20%26Ntt%3Dice%2Bmechanics"><span><span class="hlt">Ice</span> Flow in the North East Greenland <span class="hlt">Ice</span> Stream</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Joughin, Ian; Kwok, Ron; Fahnestock, M.; MacAyeal, Doug</p> <p>1999-01-01</p> <p>Early observations with ERS-1 SAR image data revealed a large <span class="hlt">ice</span> stream in North East Greenland (Fahnestock 1993). The <span class="hlt">ice</span> stream has a number of the characteristics of the more closely studied <span class="hlt">ice</span> streams in Antarctica, including its large size and gross geometry. The onset of rapid flow close to the <span class="hlt">ice</span> divide and the evolution of its flow pattern, however, make this <span class="hlt">ice</span> stream unique. These features can be seen in the balance velocities for the <span class="hlt">ice</span> stream (Joughin 1997) and its outlets. The <span class="hlt">ice</span> stream is identifiable for more than 700 km, making it much longer than any other flow feature in Greenland. Our research goals are to gain a greater understanding of the <span class="hlt">ice</span> flow in the northeast Greenland <span class="hlt">ice</span> stream and its outlet glaciers in order to assess their impact on the past, present, and future mass balance of the <span class="hlt">ice</span> sheet. We will accomplish these goals using a combination of remotely sensed data and <span class="hlt">ice</span> sheet models. We are using satellite radar interferometry data to produce a complete maps of velocity and topography over the entire <span class="hlt">ice</span> stream. We are in the process of developing methods to use these data in conjunction with existing <span class="hlt">ice</span> sheet models similar to those that have been used to improve understanding of the mechanics of flow in Antarctic <span class="hlt">ice</span> streams.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_18");'>18</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li class="active"><span>20</span></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_20 --> <div id="page_21" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="401"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19850038332&hterms=marginal&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D40%26Ntt%3Dmarginal','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19850038332&hterms=marginal&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D40%26Ntt%3Dmarginal"><span>A coupled <span class="hlt">ice</span>-ocean model of <span class="hlt">ice</span> breakup and banding in the marginal <span class="hlt">ice</span> zone</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Smedstad, O. M.; Roed, L. P.</p> <p>1985-01-01</p> <p>A coupled <span class="hlt">ice</span>-ocean numerical model for the marginal <span class="hlt">ice</span> zone is considered. The model consists of a nonlinear sea <span class="hlt">ice</span> model and a two-layer (reduced gravity) ocean model. The dependence of the upwelling response on wind stress direction is discussed. The results confirm earlier analytical work. It is shown that there exist directions for which there is no upwelling, while other directions give maximum upwelling in terms of the volume of uplifted water. The <span class="hlt">ice</span> and ocean is coupled directly through the stress at the <span class="hlt">ice</span>-ocean interface. An interesting consequence of the coupling is found in cases when the <span class="hlt">ice</span> edge is almost stationary. In these cases the <span class="hlt">ice</span> tends to break up a few tenths of kilometers inside of the <span class="hlt">ice</span> edge.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19850009740','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19850009740"><span><span class="hlt">Icing</span> flight research: Aerodynamic effects of <span class="hlt">ice</span> and <span class="hlt">ice</span> shape documentation with stereo photography</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Mikkelsen, K. L.; Mcknight, R. C.; Ranaudo, R. J.; Perkins, P. J., Jr.</p> <p>1985-01-01</p> <p>Aircraft <span class="hlt">icing</span> flight research was performed in natural <span class="hlt">icing</span> conditions. A data base consisting of <span class="hlt">icing</span> cloud measurements, <span class="hlt">ice</span> shapes, and aerodynamic measurements is being developed. During research <span class="hlt">icing</span> encounters the <span class="hlt">icing</span> cloud was continuously measured. After the encounter, the <span class="hlt">ice</span> accretion shapes on the wing were documented with a stereo camera system. The increase in wing section drag was measured with a wake survey probe. The overall aircraft performance loss in terms of lift and drag coefficient changes was obtained by steady level speed/power measurements. Selective deicing of the airframe components was performed to determine their contributions to the total drag increase. Engine out capability in terms of power available was analyzed for the <span class="hlt">iced</span> aircraft. It was shown that the stereo photography system can be used to document <span class="hlt">ice</span> shapes in flight and that the wake survey probe can measure increases in wing section drag caused by <span class="hlt">ice</span>. On one flight, the wing section drag coefficient (c sub d) increased approximately 120 percent over the uniced baseline at an aircraft angle of attack of 6 deg. On another flight, the aircraft darg coefficient (c sub d) increased by 75 percent over the uniced baseline at an aircraft lift coefficient (C sub d) of 0.5.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19850048041&hterms=photography&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DTitle%26N%3D0%26No%3D90%26Ntt%3Dphotography','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19850048041&hterms=photography&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DTitle%26N%3D0%26No%3D90%26Ntt%3Dphotography"><span><span class="hlt">Icing</span> flight research - Aerodynamic effects of <span class="hlt">ice</span> and <span class="hlt">ice</span> shape documentation with stereo photography</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Mikkelsen, K. L.; Mcknight, R. C.; Ranaudo, R. J.; Perkins, P. J., Jr.</p> <p>1985-01-01</p> <p>Aircraft <span class="hlt">icing</span> flight research was performed in natural <span class="hlt">icing</span> conditions. A data base consisting of <span class="hlt">icing</span> cloud measurements, <span class="hlt">ice</span> shapes, and aerodynamic measurements is being developed. During research <span class="hlt">icing</span> encounters the <span class="hlt">icing</span> cloud was continuously measured. After the encounter, the <span class="hlt">ice</span> accretion shapes on the wing were documented with a stereo camera system. The increase in wing section drag was measured with a wake survey probe. The overall aircraft performance loss in terms of lift and drag coefficient changes were obtained by steady level speed/power measurements. Selective deicing of the airframe components was performed to determine their contributions to the total drag increase. Engine out capability in terms of power available was analyzed for the <span class="hlt">iced</span> aircraft. It was shown that the stereo photography system can be used to document <span class="hlt">ice</span> shapes in flight and that the wake survey probe can measure increases in wing section drag caused by <span class="hlt">ice</span>. On one flight, the wing section drag coefficient (c sub d) increased approximately 120 percent over the uniced baseline at an aircraft angle of attack of 6 deg. On another flight, the aircraft drag coefficient (c sub d) increased by 75 percent over the uniced baseline at an aircraft lift coefficient (c sub d) of 0.5.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1422590-temperature-dependence-uranium-vanadium-adsorption-amidoxime-based-adsorbents-natural-seawater','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1422590-temperature-dependence-uranium-vanadium-adsorption-amidoxime-based-adsorbents-natural-seawater"><span>Temperature Dependence of Uranium and Vanadium Adsorption on Amidoxime-Based Adsorbents in Natural <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Kuo, Li-Jung; Gill, Gary A.; Tsouris, Costas</p> <p></p> <p>Recent advances in the development of amidoxime-based adsorbents have made it highly promising for <span class="hlt">seawater</span> uranium extraction. However, there is a great need to understand the influence of temperature on the uranium sequestration performance of the adsorbents in natural <span class="hlt">seawater</span>. Here in this work, the apparent enthalpy and entropy of the sorption of uranium (VI) and vanadium (V) with amidoxime-based adsorbents were determined in natural <span class="hlt">seawater</span> tests at 8, 20, and 31 °C that cover a broad range of ambient <span class="hlt">seawater</span> temperature. The sorption of U was highly endothermic, producing apparent enthalpies of 57 ± 6.0 and 59 ± 11more » kJ mol -1 and apparent entropies of 314 ± 21 and 320 ± 36 J K-1 mol -1, respectively, for two adsorbent formulations. In contrast, the sorption of V showed a much smaller temperature sensitivity, producing apparent enthalpies of 6.1 ± 5.9 and -11 ± 5.7 kJ mol -1 and apparent entropies of 164 ± 20 and 103 ± 19 J K -1 mol -1, respectively. This new thermodynamic information suggests that amidoxime-based adsorbents will deliver significantly increased U adsorption capacities and improved selectivity in warmer waters. A separate field study of <span class="hlt">seawater</span> uranium adsorption conducted in a warm <span class="hlt">seawater</span> site (Miami, FL, USA) confirm the observed strong temperature effect on <span class="hlt">seawater</span> uranium mining. Lastly, this strong temperature dependence demonstrates that the warmer the <span class="hlt">seawater</span> where the amidoxime-based adsorbents are deployed the greater the yield for <span class="hlt">seawater</span> uranium extraction.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1422590-temperature-dependence-uranium-vanadium-adsorption-amidoxime-based-adsorbents-natural-seawater','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1422590-temperature-dependence-uranium-vanadium-adsorption-amidoxime-based-adsorbents-natural-seawater"><span>Temperature Dependence of Uranium and Vanadium Adsorption on Amidoxime-Based Adsorbents in Natural <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Kuo, Li-Jung; Gill, Gary A.; Tsouris, Costas; ...</p> <p>2018-01-16</p> <p>Recent advances in the development of amidoxime-based adsorbents have made it highly promising for <span class="hlt">seawater</span> uranium extraction. However, there is a great need to understand the influence of temperature on the uranium sequestration performance of the adsorbents in natural <span class="hlt">seawater</span>. Here in this work, the apparent enthalpy and entropy of the sorption of uranium (VI) and vanadium (V) with amidoxime-based adsorbents were determined in natural <span class="hlt">seawater</span> tests at 8, 20, and 31 °C that cover a broad range of ambient <span class="hlt">seawater</span> temperature. The sorption of U was highly endothermic, producing apparent enthalpies of 57 ± 6.0 and 59 ± 11more » kJ mol -1 and apparent entropies of 314 ± 21 and 320 ± 36 J K-1 mol -1, respectively, for two adsorbent formulations. In contrast, the sorption of V showed a much smaller temperature sensitivity, producing apparent enthalpies of 6.1 ± 5.9 and -11 ± 5.7 kJ mol -1 and apparent entropies of 164 ± 20 and 103 ± 19 J K -1 mol -1, respectively. This new thermodynamic information suggests that amidoxime-based adsorbents will deliver significantly increased U adsorption capacities and improved selectivity in warmer waters. A separate field study of <span class="hlt">seawater</span> uranium adsorption conducted in a warm <span class="hlt">seawater</span> site (Miami, FL, USA) confirm the observed strong temperature effect on <span class="hlt">seawater</span> uranium mining. Lastly, this strong temperature dependence demonstrates that the warmer the <span class="hlt">seawater</span> where the amidoxime-based adsorbents are deployed the greater the yield for <span class="hlt">seawater</span> uranium extraction.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018MS%26E..370a2008T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018MS%26E..370a2008T"><span>A review of <span class="hlt">vapour</span> lock issues during motor gasoline or automotive gasoline usage in piston engine aircraft</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Thanikasalam, K.; Rahmat, M.; Fahmi, A. G. Mohammad; Zulkifli, A. M.; Shawal, N. Noor; Ilanchelvi, K.; Ananth, M.; Elayarasan, R.</p> <p>2018-05-01</p> <p>Since there is a developing practice of utilizing automotive fuels as flight fuel, there are higher chances of dangerous scenarios, particularly in the operation of piston aircraft engines. The use of motor vehicle gas (MOGAS) or aviation gas (AVGAS) in the operation of aviation piston engine increases the risk of <span class="hlt">vapour</span> locking. A statistical examination of European aviation industry indicates that around 20,000 aircraft are affected either specifically or conceivably by the different negative impacts of gasoline blended with ethanol. Particularly, for most contemporary carburettor engines, there are risks associated with ethanol-admixed fuels that have potential to upset engine operation. The danger of <span class="hlt">vapour</span> locking, which is the generation of gas bubbles inside the fuel system causing an impairment of fuel movement in the engine, is well documented particularly by studies on aircraft using MOGAS. Contrasted with AVGAS, MOGAS is inclined to demonstrate this phenomenon. <span class="hlt">Vapour</span> lock is perhaps the leading serious problem that ought to be addressed if MOGAS is to be used as a substitute for AVGAS. <span class="hlt">Vapour</span> lock problem is critical because it causes malfunctions to aircraft engines. Thus, an understanding of <span class="hlt">vapour</span> handling ability of small aircraft is essential to establish safe operating confines at existing fuel temperature and pressures.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28513739','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28513739"><span><span class="hlt">Vapour</span>-liquid interfacial properties of square-well chains from density functional theory and Monte Carlo simulation.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Martínez-Ruiz, Francisco José; Blas, Felipe J; Moreno-Ventas Bravo, A Ignacio; Míguez, José Manuel; MacDowell, Luis G</p> <p>2017-05-17</p> <p>The statistical associating fluid theory for attractive potentials of variable range (SAFT-VR) density functional theory (DFT) developed by [Gloor et al., J. Chem. Phys., 2004, 121, 12740-12759] is used to predict the interfacial behaviour of molecules modelled as fully-flexible square-well chains formed from tangentially-bonded monomers of diameter σ and potential range λ = 1.5σ. Four different model systems, comprising 4, 8, 12, and 16 monomers per molecule, are considered. In addition to that, we also compute a number of interfacial properties of molecular chains from direct simulation of the <span class="hlt">vapour</span>-liquid interface. The simulations are performed in the canonical ensemble, and the <span class="hlt">vapour</span>-liquid interfacial tension is evaluated using the wandering interface (WIM) method, a technique based on the thermodynamic definition of surface tension. Apart from surface tension, we also obtain density profiles, coexistence densities, <span class="hlt">vapour</span> pressures, and critical temperature and density, paying particular attention to the effect of the chain length on these properties. According to our results, the main effect of increasing the chain length (at fixed temperature) is to sharpen the <span class="hlt">vapour</span>-liquid interface and to increase the width of the biphasic coexistence region. As a result, the interfacial thickness decreases and the surface tension increases as the molecular chains get longer. The interfacial thickness and surface tension appear to exhibit an asymptotic limiting behaviour for long chains. A similar behaviour is also observed for the coexistence densities and critical properties. Agreement between theory and simulation results indicates that SAFT-VR DFT is only able to predict qualitatively the interfacial properties of the model. Our results are also compared with simulation data taken from the literature, including the <span class="hlt">vapour</span>-liquid coexistence densities, <span class="hlt">vapour</span> pressures, and surface tension.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29263764','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29263764"><span>UTLS water <span class="hlt">vapour</span> from SCIAMACHY limb measurementsV3.01 (2002-2012).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Weigel, K; Rozanov, A; Azam, F; Bramstedt, K; Damadeo, R; Eichmann, K-U; Gebhardt, C; Hurst, D; Kraemer, M; Lossow, S; Read, W; Spelten, N; Stiller, G P; Walker, K A; Weber, M; Bovensmann, H; Burrows, J P</p> <p>2016-01-01</p> <p>The SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) aboard the Envisat satellite provided measurements from August 2002 until April 2012. SCIAMACHY measured the scattered or direct sunlight using different observation geometries. The limb viewing geometry allows the retrieval of water <span class="hlt">vapour</span> at about 10-25 km height from the near-infrared spectral range (1353-1410 nm). These data cover the upper troposphere and lower stratosphere (UTLS), a region in the atmosphere which is of special interest for a variety of dynamical and chemical processes as well as for the radiative forcing. Here, the latest data version of water <span class="hlt">vapour</span> (V3.01) from SCIAMACHY limb measurements is presented and validated by comparisons with data sets from other satellite and in situ measurements. Considering retrieval tests and the results of these comparisons, the V3.01 data are reliable from about 11 to 23 km and the best results are found in the middle of the profiles between about 14 and 20 km. Above 20 km in the extra tropics V3.01 is drier than all other data sets. Additionally, for altitudes above about 19 km, the vertical resolution of the retrieved profile is not sufficient to resolve signals with a short vertical structure like the tape recorder. Below 14 km, SCIAMACHY water <span class="hlt">vapour</span> V3.01 is wetter than most collocated data sets, but the high variability of water <span class="hlt">vapour</span> in the troposphere complicates the comparison. For 14-20 km height, the expected errors from the retrieval and simulations and the mean differences to collocated data sets are usually smaller than 10 % when the resolution of the SCIAMACHY data is taken into account. In general, the temporal changes agree well with collocated data sets except for the Northern Hemisphere extratropical stratosphere, where larger differences are observed. This indicates a possible drift in V3.01 most probably caused by the incomplete treatment of volcanic aerosols in the retrieval. In all other regions a</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/16357267','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/16357267"><span><span class="hlt">Ice</span> recrystallization inhibition in <span class="hlt">ice</span> cream as affected by <span class="hlt">ice</span> structuring proteins from winter wheat grass.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Regand, A; Goff, H D</p> <p>2006-01-01</p> <p><span class="hlt">Ice</span> recrystallization in quiescently frozen sucrose solutions that contained some of the ingredients commonly found in <span class="hlt">ice</span> cream and in <span class="hlt">ice</span> cream manufactured under commercial conditions, with or without <span class="hlt">ice</span> structuring proteins (ISP) from cold-acclimated winter wheat grass extract (AWWE), was assessed by bright field microscopy. In sucrose solutions, critical differences in moisture content, viscosity, ionic strength, and other properties derived from the presence of other ingredients (skim milk powder, corn syrup solids, locust bean gum) caused a reduction in <span class="hlt">ice</span> crystal growth. Significant ISP activity in retarding <span class="hlt">ice</span> crystal growth was observed in all solutions (44% for the most complex mix) containing 0.13% total protein from AWWE. In heat-shocked <span class="hlt">ice</span> cream, <span class="hlt">ice</span> recrystallization rates were significantly reduced 40 and 46% with the addition of 0.0025 and 0.0037% total protein from AWWE. The ISP activity in <span class="hlt">ice</span> cream was not hindered by its inclusion in mix prior to pasteurization. A synergistic effect between ISP and stabilizer was observed, as ISP activity was reduced in the absence of stabilizer in <span class="hlt">ice</span> cream formulations. A remarkably smoother texture for <span class="hlt">ice</span> creams containing ISP after heat-shock storage was evident by sensory evaluation. The efficiency of ISP from AWWE in controlling <span class="hlt">ice</span> crystal growth in <span class="hlt">ice</span> cream has been demonstrated.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1994RaPC...43..249T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1994RaPC...43..249T"><span>Physical and biological characterization of a <span class="hlt">seawater</span> ultraviolet radiation sterilizer</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Torrentera, Laura; Uribe, Roberto M.; Rodríguez, Romana R.; Carrillo, Ricardo E.</p> <p>1994-03-01</p> <p>The physical and biological characterization of a <span class="hlt">seawater</span> ultraviolet (UV) sterilizer is described. The physical characterization was performed using radiochromic dye films by evaluating the uniformity of the radiant exposure along each lamp, the effect of the radiation from one lamp on the array of adjacent lamps, and by measuring the UV radiation absorption of <span class="hlt">seawater</span> with respect to distilled water. The biological characterization was performed by measuring the amount of reduction of bacteria in stored <span class="hlt">seawater</span> after different filtration and UV treatments. Among the filtration methods tested, differential filtration (5, 3 and 0.45 μm filters connected in series) caused the highest bacterial reduction factor of 60%. UV radiant exposures of 212, 424, 636 and 848 J m -2 yielded bacteria reduction factors of 99.86, 99.969, 99.997 and 100%, respectively, for populations of Vibrio and Pseudomonas bacteria present in stored <span class="hlt">seawater</span>. It is concluded that the system is useful for water disinfection when 1, 2 or 3 lamps are on; when 4 lamps are used the treated water becomes sterile.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018JGRC..123.1586G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018JGRC..123.1586G"><span>Atmosphere-<span class="hlt">Ice</span>-Ocean-Ecosystem Processes in a Thinner Arctic Sea <span class="hlt">Ice</span> Regime: The Norwegian Young Sea <span class="hlt">ICE</span> (N-<span class="hlt">ICE</span>2015) Expedition</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Granskog, Mats A.; Fer, Ilker; Rinke, Annette; Steen, Harald</p> <p>2018-03-01</p> <p>Arctic sea <span class="hlt">ice</span> has been in rapid decline the last decade and the Norwegian young sea <span class="hlt">ICE</span> (N-<span class="hlt">ICE</span>2015) expedition sought to investigate key processes in a thin Arctic sea <span class="hlt">ice</span> regime, with emphasis on atmosphere-snow-<span class="hlt">ice</span>-ocean dynamics and sea <span class="hlt">ice</span> associated ecosystem. The main findings from a half-year long campaign are collected into this special section spanning the Journal of Geophysical Research: Atmospheres, Journal of Geophysical Research: Oceans, and Journal of Geophysical Research: Biogeosciences and provide a basis for a better understanding of processes in a thin sea <span class="hlt">ice</span> regime in the high Arctic. All data from the campaign are made freely available to the research community.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70013153','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70013153"><span>Time and the crystallization of apatite in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Gulbrandsen, R.A.; Roberson, C.E.; Neil, S.T.</p> <p>1984-01-01</p> <p>Carbonate fluorapatite has been synthesized in <span class="hlt">seawater</span> in an experiment of nearly 10-years duration. The addition of phosphate to <span class="hlt">seawater</span> whose fluoride concentration had been increased to 7.6 mg/l brought about an initial amorphous phosphate precipitate. After 20 months, a crystalline magnesium phosphate phase developed within the amorphous phosphate. Crystallization of apatite, which occurred during the last 3 years of the experiment, was accompanied by dissolution of the crystalline magnesium phosphate phase. The MgO content of the apatite (1.9 percent) is high in comparison to Tertiary and older apatite but similar to some young apatite; the CO2 content (3.6 percent) is medium, and the fluorine content (2.2 percent) is low but again similar to some young apatite. The hydroxyl ion (OH-) likely fills the need for additional fluorine-position atoms. The mole ratio of Ca plus substituent elements to P plus substituent elements (1.50) is low in comparison to the expected ratio of 1.67. The substitution of the hydronium ion (H3O+) for Ca may account for this difference. The synthesis of apatite in <span class="hlt">seawater</span> demonstrates that the factor of time overcomes the well known inhibiting effect of magnesium upon the crystallization of apatite. It also implies that given an adequate supply of phosphate, apatite can form in most ocean environments and likely plays a major pan in the control of the phosphate content of <span class="hlt">seawater</span>. ?? 1984.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2009EGUGA..1110465F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2009EGUGA..1110465F"><span>Raman scattering investigations of the interaction of a COV with pure and acid doped <span class="hlt">ice</span> particles</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Facq, S.; Oancea, A.; Focsa, C.; Chazallon, B.</p> <p>2009-04-01</p> <p><span class="hlt">Ice</span> present in polar stratosphere is as well a common component of the troposphere, particularly in cirrus clouds widespread in tropopause and upper troposphere region. With water droplets, <span class="hlt">ice</span> constitutes the condensed matter that can interact with atmospheric trace gases via many different trapping processes (co-deposition i.e; incorporation during growing <span class="hlt">ice</span> conditions, adsorption, freezing etc). The incorporation of trace gases in <span class="hlt">ice</span> surface/volume can both affect the atmospheric chemistry and the <span class="hlt">ice</span> structure and reactivity. This can therefore modify the nature and composition of the incorporated species in <span class="hlt">ice</span>, or in the gas phase. Recently, field measurements have demonstrated the presence of nitric acid in <span class="hlt">ice</span> particles from cirrus clouds(1,2) (concentration between 0.63 wt% and 2.5 wt %). Moreover, laboratory experiments have shown that the uptake of atmospheric trace gases can be enhanced up to 1 or 2 orders of magnitude in these doped <span class="hlt">ice</span> particles. Among trace gases capable to interact with atmospheric condensed matter figure volatile organic compounds such as aldehydes, ketones and alcohols (ex: ethanol and methanol). They play an important role in the upper troposphere (3,4) and snowpack chemistry (5) as they can be easily photolysed, producing free radicals and so influence the oxidizing capacity and the ozone-budget of the atmosphere (3,4). The temperature range at which these physico-chemical processes occur extents between ~ 190 K and 273K. Interaction between <span class="hlt">ice</span> and trace gases are therefore largely dependent on the <span class="hlt">ice</span> surface properties as well as on the phase formation dynamic (crystalline or not). This study aims to examine and characterize the incorporation of a COV (ex: ethanol), at the surface or in the volume of <span class="hlt">ice</span> formed by different growth mechanisms (<span class="hlt">vapour</span> deposition or droplets freezing). Vibrational spectra of water OH and ethanol CH-spectral regions are analysed using confocal micro-Raman spectroscopy at different temperatures</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1986CoMP...94..317T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1986CoMP...94..317T"><span><span class="hlt">Vapour</span> loss (``boiling'') as a mechanism for fluid evolution in metamorphic rocks</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Trommsdorff, Volkmar; Skippen, George</p> <p>1986-11-01</p> <p>The calculation of fluid evolution paths during reaction progress is considered for multicomponent systems and the results applied to the ternary system, CO2-H2O-NaCl. Fluid evolution paths are considered for systems in which a CO2-rich phase of lesser density (<span class="hlt">vapour</span>) is preferentially removed from the system leaving behind a saline aqueous phase (liquid). Such “boiling” leads to enrichment of the residual aqueous phase in dissolved components and, for certain reaction stoichiometries, to eventual saturation of the fluids in salt components. Distinctive textures, particularly radiating growths of prismatic minerals such as tremolite or diopside, are associated with saline fluid inclusions and solid syngenetic salt inclusions at a number of field localities. The most thoroughly studied of these localities is Campolungo, Switzerland, where metasomatic rocks have developed in association with fractures and veins at 500° C and 2,000 bars of pressure. The petrography of these rocks suggests that fluid phase separation into liquid and <span class="hlt">vapour</span> has been an important process during metasomatism. Fracture systems with fluids at pressure less than lithostatic may facilitate the loss of the less dense <span class="hlt">vapour</span> phase to conditions of the amphibolite facies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70021497','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70021497"><span>Reassessment of <span class="hlt">ice</span>-age cooling of the tropical ocean and atmosphere</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Hostetler, S.W.; Mix, A.C.</p> <p>1999-01-01</p> <p>The CLIMAP project's reconstruction of past sea surface temperature inferred limited <span class="hlt">ice</span>-age cooling in the tropical oceans. This conclusion has been controversial, however, because of the greater cooling indicated by other terrestrial and ocean proxy data. A new faunal sea surface temperature reconstruction, calibrated using the variation of foraminiferal species through time, better represents <span class="hlt">ice</span>-age faunal assemblages and so reveals greater cooling than CLIMAP in the equatorial current systems of the eastern Pacific and tropical Atlantic oceans. Here we explore the climatic implications of this revised sea surface temperature field for the Last Glacial Maximum using an atmospheric general circulation model. Relative to model results obtained using CLIMAP sea surface temperatures, the cooler equatorial oceans modify seasonal air temperatures by 1-2??C or more across parts of South America, Africa and southeast Asia and cause attendant changes in regional moisture patterns. In our simulation of the Last Glacial Maximum, the Amazon lowlands, for example, are cooler and drier, whereas the Andean highlands are cooler and wetter than the control simulation. Our results may help to resolve some of the apparent disagreements between oceanic and continental proxy climate data. Moreover, they suggest a wind-related mechanism for enhancing the export of water <span class="hlt">vapour</span> from the Atlantic to the Indo-Pacific oceans, which may link variations in deep-water production and high-latitude climate changes to equatorial sea surface temperatures.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25437762','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25437762"><span>The delivery of organic contaminants to the Arctic food web: why sea <span class="hlt">ice</span> matters.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Pućko, Monika; Stern, Gary A; Macdonald, Robie W; Jantunen, Liisa M; Bidleman, Terry F; Wong, Fiona; Barber, David G; Rysgaard, Søren</p> <p>2015-02-15</p> <p>For decades sea <span class="hlt">ice</span> has been perceived as a physical barrier for the loading of contaminants to the Arctic Ocean. We show that sea <span class="hlt">ice</span>, in fact, facilitates the delivery of organic contaminants to the Arctic marine food web through processes that: 1) are independent of contaminant physical-chemical properties (e.g. 2-3-fold increase in exposure to brine-associated biota), and 2) depend on physical-chemical properties and, therefore, differentiate between contaminants (e.g. atmospheric loading of contaminants to melt ponds over the summer, and their subsequent leakage to the ocean). We estimate the concentrations of legacy organochlorine pesticides (OCPs) and current-use pesticides (CUPs) in melt pond water in the Beaufort Sea, Canadian High Arctic, in 2008, at near-gas exchange equilibrium based on Henry's law constants (HLCs), air concentrations and exchange dynamics. CUPs currently present the highest risk of increased exposures through melt pond loading and drainage due to the high ratio of melt pond water to <span class="hlt">seawater</span> concentration (Melt pond Enrichment Factor, MEF), which ranges from 2 for dacthal to 10 for endosulfan I. Melt pond contaminant enrichment can be perceived as a hypothetical 'pump' delivering contaminants from the atmosphere to the ocean under <span class="hlt">ice</span>-covered conditions, with 2-10% of CUPs annually entering the Beaufort Sea via this input route compared to the standing stock in the Polar Mixed Layer of the ocean. The abovementioned processes are strongly favored in first-year <span class="hlt">ice</span> compared to multi-year <span class="hlt">ice</span> and, therefore, the dynamic balance between contaminant inventories and contaminant deposition to the surface ocean is being widely affected by the large-scale icescape transition taking place in the Arctic. Copyright © 2014 Elsevier B.V. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20080044852','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20080044852"><span>Accurate L-Band Measurements of the Dielectric Constant of <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Lang, R.H.; Utku, C.; Tarkocin, Y.; Vine, D.M. Le</p> <p>2007-01-01</p> <p>A new temperature controlled microwave cavity system to measure the complex dielectric constant of <span class="hlt">seawater</span> at 1.413 GHz is discussed. The system is being developed to measure <span class="hlt">seawater</span> for temperatures from O C to 30 C and salinities from 10 to 40 psu, The paper discusses the construction of the measurement system and initial stability tests.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/29023825','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/29023825"><span>Gen<span class="hlt">Ice</span>: Hydrogen-Disordered <span class="hlt">Ice</span> Generator.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Matsumoto, Masakazu; Yagasaki, Takuma; Tanaka, Hideki</p> <p>2018-01-05</p> <p>Gen<span class="hlt">Ice</span> is an efficient and user-friendly tool to generate hydrogen-disordered <span class="hlt">ice</span> structures. It makes <span class="hlt">ice</span> and clathrate hydrate structures in various file formats. More than 100 kinds of structures are preset. Users can install their own crystal structures, guest molecules, and file formats as plugins. The algorithm certifies that the generated structures are completely randomized hydrogen-disordered networks obeying the <span class="hlt">ice</span> rule with zero net polarization. © 2017 The Authors. Journal of Computational Chemistry Published by Wiley Periodicals, Inc. © 2017 The Authors. Journal of Computational Chemistry Published by Wiley Periodicals, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015GeoRL..42.5442L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015GeoRL..42.5442L"><span>Observed platelet <span class="hlt">ice</span> distributions in Antarctic sea <span class="hlt">ice</span>: An index for ocean-<span class="hlt">ice</span> shelf heat flux</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Langhorne, P. J.; Hughes, K. G.; Gough, A. J.; Smith, I. J.; Williams, M. J. M.; Robinson, N. J.; Stevens, C. L.; Rack, W.; Price, D.; Leonard, G. H.; Mahoney, A. R.; Haas, C.; Haskell, T. G.</p> <p>2015-07-01</p> <p>Antarctic sea <span class="hlt">ice</span> that has been affected by supercooled <span class="hlt">Ice</span> Shelf Water (ISW) has a unique crystallographic structure and is called platelet <span class="hlt">ice</span>. In this paper we synthesize platelet <span class="hlt">ice</span> observations to construct a continent-wide map of the winter presence of ISW at the ocean surface. The observations demonstrate that, in some regions of coastal Antarctica, supercooled ISW drives a negative oceanic heat flux of -30 Wm-2 that persists for several months during winter, significantly affecting sea <span class="hlt">ice</span> thickness. In other regions, particularly where the thinning of <span class="hlt">ice</span> shelves is believed to be greatest, platelet <span class="hlt">ice</span> is not observed. Our new data set includes the longest <span class="hlt">ice</span>-ocean record for Antarctica, which dates back to 1902 near the McMurdo <span class="hlt">Ice</span> Shelf. These historical data indicate that, over the past 100 years, any change in the volume of very cold surface outflow from this <span class="hlt">ice</span> shelf is less than the uncertainties in the measurements.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70025479','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70025479"><span>An experimental investigation of barite formation in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Ganeshram, R.S.; Francois, R.; Commeau, J.; Brown-Leger, S. L.</p> <p>2003-01-01</p> <p>We report results from time-series decay and sequential leaching experiments of laboratory cultured and coastal plankton to elucidate the mechanisms controlling barite formation in <span class="hlt">seawater</span>. Batch-cultured diatoms ( Stephanopyxis palmerina ) and coccolithophorids (Emiliania huxleyi) were let to decay in the dark for 8-10 weeks, suspended in aerated <span class="hlt">seawater</span>. The development of barite crystals was monitored by Scanning Electron Microscopy (SEM). A similar experiment was conducted with plankton collected during the spring-bloom in Vineyard Sound (MA). In addition to SEM, suspended particles were sequentially leached for Ba (distilled water rinse; 10% (v/v) HNO3 rinse at room temperature; 30% (v/v) HCl at 80??C overnight; 50% (v/v) HNO3 at 80??C overnight) immediately after collection, and after 10-week decay in <span class="hlt">seawater</span>, in <span class="hlt">seawater</span> poisoned with HgCl2, and in <span class="hlt">seawater</span> spiked with 135Ba. Both experiments showed an increase in the number of barite crystals during decay. The spring-bloom plankton had initially a large pool of labile Ba, soluble in distilled water and cold dilute HNO3 that was lost from the plankton after 10-week decay in both axenic and nonaxenic conditions. In contrast, Ba in the decayed plankton samples was predominantly in forms extracted by hot HCl and hot HNO3 acids, which were attributed to presence of barite Ba and refractory organic Ba respectively. The increase in barite crystal counts under a Scanning Electron Microscope (SEM), the increase in HCl extractable Ba relative to organic carbon, and the loss of a large fraction of Ba during plankton decay suggest that living plankton consists of a relatively large pool of labile Ba, which is rapidly released during plankton decomposition and acts as the main source of Ba for barite formation in supersaturated microenvironments. Since mass balance indicates that only a small proportion (2 to 4%) of the labile-Ba pool is converted to barite, the availability of microenvironments that could locally</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_19");'>19</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li class="active"><span>21</span></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_21 --> <div id="page_22" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="421"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=128817&keyword=consumer+AND+reports&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50','EPA-EIMS'); return false;" href="https://cfpub.epa.gov/si/si_public_record_report.cfm?dirEntryId=128817&keyword=consumer+AND+reports&actType=&TIMSType=+&TIMSSubTypeID=&DEID=&epaNumber=&ntisID=&archiveStatus=Both&ombCat=Any&dateBeginCreated=&dateEndCreated=&dateBeginPublishedPresented=&dateEndPublishedPresented=&dateBeginUpdated=&dateEndUpdated=&dateBeginCompleted=&dateEndCompleted=&personID=&role=Any&journalID=&publisherID=&sortBy=revisionDate&count=50"><span>THE INTERACTION OF <span class="hlt">VAPOUR</span> PHASE ORGANIC COMPOUNDS WITH INDOOR SINKS</span></a></p> <p><a target="_blank" href="http://oaspub.epa.gov/eims/query.page">EPA Science Inventory</a></p> <p></p> <p></p> <p>The interaction of indoor air pollutants with interior surfaces (i.e., sinks) is a well known, but poorly understood, phenomenon. Studies have shown that re-emissions of adsorbed organic <span class="hlt">vapours</span> can contribute to elevated concentrations of organics in indoor environments. Researc...</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016AGUOSMM44B0486L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016AGUOSMM44B0486L"><span>Effects of Chemical Structure on Hydrolysis Pathways of Small Peptides in Coastal <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Liu, S.; Reyna, N. E.; Hamdan, L. J.; Liu, Z.</p> <p>2016-02-01</p> <p>Deciphering peptide hydrolysis pathways is key to understanding the mechanism of peptide hydrolysis, in particular the types of extracellular enzymes that are active in <span class="hlt">seawater</span>. From the hydrolyzed fragments of small peptides, one can estimate the role of amino-, carboxy-, and endopeptidases in a quantitative way. In this study, we incubated several small peptides with different amino acid compositions, alanine-valine-phenylalanine-alanine (AVFA), phenylalanine-alanine-serine-tryptophan-glycine-alanine (FASWGA), VFA, SWGA, VVFA, arginine-valine-phenylalanine-alanine (RVFA), SVFA, aspartic acid-valine-phenylalanine-alanine (DVFA), trialanine (AAA), and AVF in two coastal <span class="hlt">seawaters</span> (ship channel <span class="hlt">seawater</span> in the western Gulf of Mexico and Sta. C6 <span class="hlt">seawater</span> in the northern Gulf of Mexico). In both <span class="hlt">seawaters</span>, aminopeptidases played a more dominant role (22-67%) in hydrolyzing peptides with hydrophobic amino acid at the N-terminus, such as AVFA, VVFA, VFA, and AAA, or with basic amino acid at the N-terminus (RVFA), as compared to those with N-terminal polar amino acid (SVFA, SWGA) or acidic amino acid (DVFA) (0-24%). This result indicates that amino acid composition in a peptide structure affects how the peptide is hydrolyzed. We also found that peptides in the C6 <span class="hlt">seawater</span> were hydrolyzed dominantly by aminopeptidases (10-59%), while those in the ship channel <span class="hlt">seawater</span> also by endo- or carboxypeptidases (9-69%). This pattern suggests that peptide hydrolysis pathways depend on specific environment conditions, such as bacterial community structure, that can lead to variations in abundances or activities among amino-, carboxy- and endopeptidases. Overall, the results provide insights into the effects of chemical structure and <span class="hlt">seawater</span> environment on peptide hydrolysis pathways.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19930022699&hterms=stream+box&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dstream%2Bbox','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19930022699&hterms=stream+box&qs=N%3D0%26Ntk%3DAll%26Ntx%3Dmode%2Bmatchall%26Ntt%3Dstream%2Bbox"><span>The mass balance of the <span class="hlt">ice</span> plain of <span class="hlt">Ice</span> Stream B and Crary <span class="hlt">Ice</span> Rise</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Bindschadler, Robert</p> <p>1993-01-01</p> <p>The region in the mouth of <span class="hlt">Ice</span> Stream B (the <span class="hlt">ice</span> plain) and that in the vicinity of Crary <span class="hlt">Ice</span> Rise are experiencing large and rapid changes. Based on velocity, <span class="hlt">ice</span> thickness, and accumulation rate data, the patterns of net mass balance in these regions were calculated. Net mass balance, or the rate of <span class="hlt">ice</span> thickness change, was calculated as the residual of all mass fluxes into and out of subregions (or boxes). Net mass balance provides a measure of the state of health of the <span class="hlt">ice</span> sheet and clues to the current dynamics.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JPS...342...79L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JPS...342...79L"><span>High-temperature electrolysis of synthetic <span class="hlt">seawater</span> using solid oxide electrolyzer cells</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lim, Chee Kuan; Liu, Qinglin; Zhou, Juan; Sun, Qiang; Chan, Siew Hwa</p> <p>2017-02-01</p> <p>A Ni-YSZ/YSZ/LSCF-GDC solid oxide electrolyzer cell (SOEC) is used to investigate the effects of <span class="hlt">seawater</span> electrolysis for hydrogen production through electrolyzing steam produced from simulated <span class="hlt">seawater</span> bath. Steam electrolysis using an SOEC with its fuel electrode contaminated by sea salt is also investigated. Steam produced from <span class="hlt">seawater</span> is found to be free of contaminants, which are present in the <span class="hlt">seawater</span>. Similar electrochemical performance is observed from the polarization curves and impedance spectra when using steam produced from pure water and <span class="hlt">seawater</span>. Their short-term degradation rates are similar, which are registered at 15% 1000 h-1 for both cases. For the case of direct sea salt contamination in an SOEC's fuel electrode, both the uncontaminated and contaminated cells exhibit rather similar performance as observed from the polarization curves and impedance spectra. The difference in ASR values from the polarization curves and impedance spectra between the uncontaminated and contaminated cell are all within a 10% range. Rather similar short-term degradation rates of 15% 1000 h-1 and 16% 1000 h-1 are recorded for the uncontaminated and contaminated cells, respectively. Post-mortem analysis shows that the sea salt impregnated into the cell has been vaporized at a typical SOEC operating temperature of 800 °C over the period of operation.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/ADA108588','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/ADA108588"><span>Study of Laser Created Metal <span class="hlt">Vapour</span> Plasmas.</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>1981-09-01</p> <p>ance saturation could lead to extensive ground Zcvei burnout of certain kinds of atoms or ions and that this could lead to the creation of a ground...level FORM DD I JAN ", 1473 UNCLASSIFIED SECURITY CLASSIFICATION OF THIS PACE ’l hen Dota Fnt ’UNCLASSIFIFD SS ~eUItTY CLASSIFICATION OF THIS PAqE(W"Sef...<span class="hlt">vapours</span>. Preliminary calculations have suggested that laser resonance saturation could lead to extensive ground level burnout of certain kinds of</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22551178-transversely-diode-pumped-alkali-metal-vapour-laser','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22551178-transversely-diode-pumped-alkali-metal-vapour-laser"><span>Transversely diode-pumped alkali metal <span class="hlt">vapour</span> laser</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Parkhomenko, A I; Shalagin, A M</p> <p>2015-09-30</p> <p>We have studied theoretically the operation of a transversely diode-pumped alkali metal <span class="hlt">vapour</span> laser. For the case of high-intensity laser radiation, we have obtained an analytical solution to a complex system of differential equations describing the laser. This solution allows one to exhaustively determine all the energy characteristics of the laser and to find optimal parameters of the working medium and pump radiation (temperature, buffer gas pressure, and intensity and width of the pump spectrum). (lasers)</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017EGUGA..1916019G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017EGUGA..1916019G"><span>The effect on Arctic climate of atmospheric meridional energy-transport changes studied based on the CESM climate model</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Grand Graversen, Rune</p> <p>2017-04-01</p> <p>The Arctic amplification of global warming, and the pronounced Arctic sea-<span class="hlt">ice</span> retreat constitute some of the most alarming signs of global climate change. These Arctic changes are likely a consequence of a combination of several processes, for instance enhanced uptake of solar radiation in the Arctic due to a decrease of sea <span class="hlt">ice</span> (the <span class="hlt">ice</span>-albedo feedback), and increase in the local Arctic greenhouse effect due to enhanced moister flux from lower latitudes. Many of the proposed processes appear to be dependent on each other, for instance an increase in water-<span class="hlt">vapour</span> advection to the Arctic enhances the greenhouse effect in the Arctic and the longwave radiation to the surface, leading to sea-<span class="hlt">ice</span> melt and enhancement of the <span class="hlt">ice</span>-albedo feedback. The effects of albedo changes and other radiative feedbacks have been investigated in earlier studies based on model experiments designed to examine these effects specifically. Here we instead focus on the effects of meridional transport changes into the Arctic, both of moister and dry-static energy. Hence we here present results of model experiments with the CESM climate model designed specifically to extract the effects of the changes of the two transport components. In the CESM model the moister transport to the Arctic increases, whereas the dry-static transport decreases in response to a doubling of CO2. This is in agreement with other model results. The model is now forced with these transport changes of water-<span class="hlt">vapour</span> and dry-static energy associated with a CO2 doubling. The results show that changes of the water-<span class="hlt">vapour</span> transport lead to Arctic warming. This is partly a consequence of the <span class="hlt">ice</span>-albedo feedback due to sea-<span class="hlt">ice</span> melt caused by the change of the water-<span class="hlt">vapour</span> advection. The changes of the dry-static transport lead to Arctic cooling, which however is smaller than the warming induced by the water-<span class="hlt">vapour</span> component. Hence this study support the hypothesis that changes in the atmospheric circulation contribute to the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004AGUSM.C42A..02D','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004AGUSM.C42A..02D"><span>Operationally Monitoring Sea <span class="hlt">Ice</span> at the Canadian <span class="hlt">Ice</span> Service</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>de Abreu, R.; Flett, D.; Carrieres, T.; Falkingham, J.</p> <p>2004-05-01</p> <p>The Canadian <span class="hlt">Ice</span> Service (CIS) of the Meteorological Service of Canada promotes safe and efficient maritime operations and protects Canada's environment by providing reliable and timely information about <span class="hlt">ice</span> and iceberg conditions in Canadian waters. Daily and seasonal charts describing the extent, type and concentration of sea <span class="hlt">ice</span> and icebergs are provided to support navigation and other activities (e.g. oil and gas) in coastal waters. The CIS relies on a suite of spaceborne visible, infrared and microwave sensors to operationally monitor <span class="hlt">ice</span> conditions in Canadian coastal and inland waterways. These efforts are complemented by operational sea <span class="hlt">ice</span> models that are customized and run at the CIS. The archive of these data represent a 35 year archive of <span class="hlt">ice</span> conditions and have proven to be a valuable dataset for historical sea <span class="hlt">ice</span> analysis. This presentation will describe the daily integration of remote sensing observations and modelled <span class="hlt">ice</span> conditions used to produce <span class="hlt">ice</span> and iceberg products. A review of the decadal evolution of this process will be presented, as well as a glimpse into the future of <span class="hlt">ice</span> and iceberg monitoring. Examples of the utility of the CIS digital sea <span class="hlt">ice</span> archive for climate studies will also be presented.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25529334','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25529334"><span>Nano-micro structured superhydrophobic zinc coating on steel for prevention of corrosion and <span class="hlt">ice</span> adhesion.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Brassard, J D; Sarkar, D K; Perron, J; Audibert-Hayet, A; Melot, D</p> <p>2015-06-01</p> <p>Thin films of zinc have been deposited on steel substrates by electrodeposition process and further functionalized with ultra-thin films of commercial silicone rubber, in order to obtain superhydrophobic properties. Morphological feature, by scanning electron microscope (SEM), shows that the electrodeposited zinc films are composed of micro-nano rough patterns. Furthermore, chemical compositions of these films have been analyzed by X-ray diffraction (XRD) and infra-red (IRRAS). An optimum electrodeposition condition, based on electrical potential and deposition time, has been obtained which provides superhydrophobic properties with a water contact angle of 155±1°. The corrosion resistance properties, in artificial <span class="hlt">seawater</span>, of the superhydrophobic zinc coated steel are found to be superior to bare steel. Similarly, the measured <span class="hlt">ice</span> adhesion strength on superhydrophobic surfaces, using the centrifugal adhesion test (CAT), is found to be 6.3 times lower as compared to bare steel. This coating has promising applications in offshore environment, to mitigate corrosion and reduce <span class="hlt">ice</span> adhesion. Copyright © 2014 Elsevier Inc. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20050179461','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20050179461"><span>Sea <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Parkinson, Claire L.; Cavalieri, Donald J.</p> <p>2005-01-01</p> <p>Sea <span class="hlt">ice</span> covers vast areas of the polar oceans, with <span class="hlt">ice</span> extent in the Northern Hemisphere ranging from approximately 7 x 10(exp 6) sq km in September to approximately 15 x 10(exp 6) sq km in March and <span class="hlt">ice</span> extent in the Southern Hemisphere ranging from approximately 3 x 10(exp 6) sq km in February to approximately 18 x 10(exp 6) sq km in September. These <span class="hlt">ice</span> covers have major impacts on the atmosphere, oceans, and ecosystems of the polar regions, and so as changes occur in them there are potential widespread consequences. Satellite data reveal considerable interannual variability in both polar sea <span class="hlt">ice</span> covers, and many studies suggest possible connections between the <span class="hlt">ice</span> and various oscillations within the climate system, such as the Arctic Oscillation, North Atlantic Oscillation, and Antarctic Oscillation, or Southern Annular Mode. Nonetheless, statistically significant long-term trends are also apparent, including overall trends of decreased <span class="hlt">ice</span> coverage in the Arctic and increased <span class="hlt">ice</span> coverage in the Antarctic from late 1978 through the end of 2003, with the Antarctic <span class="hlt">ice</span> increases following marked decreases in the Antarctic <span class="hlt">ice</span> during the 1970s. For a detailed picture of the seasonally varying <span class="hlt">ice</span> cover at the start of the 21st century, this chapter includes <span class="hlt">ice</span> concentration maps for each month of 2001 for both the Arctic and the Antarctic, as well as an overview of what the satellite record has revealed about the two polar <span class="hlt">ice</span> covers from the 1970s through 2003.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016CorRe..35.1311P','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016CorRe..35.1311P"><span>Differential modification of <span class="hlt">seawater</span> carbonate chemistry by major coral reef benthic communities</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Page, Heather N.; Andersson, Andreas J.; Jokiel, Paul L.; Rodgers, Ku'ulei S.; Lebrato, Mario; Yeakel, Kiley; Davidson, Charlie; D'Angelo, Sydney; Bahr, Keisha D.</p> <p>2016-12-01</p> <p>Ocean acidification (OA) resulting from uptake of anthropogenic CO2 may negatively affect coral reefs by causing decreased rates of biogenic calcification and increased rates of CaCO3 dissolution and bioerosion. However, in addition to the gradual decrease in <span class="hlt">seawater</span> pH and Ω a resulting from anthropogenic activities, <span class="hlt">seawater</span> carbonate chemistry in these coastal ecosystems is also strongly influenced by the benthic metabolism which can either exacerbate or alleviate OA through net community calcification (NCC = calcification - CaCO3 dissolution) and net community organic carbon production (NCP = primary production - respiration). Therefore, to project OA on coral reefs, it is necessary to understand how different benthic communities modify the reef <span class="hlt">seawater</span> carbonate chemistry. In this study, we used flow-through mesocosms to investigate the modification of <span class="hlt">seawater</span> carbonate chemistry by benthic metabolism of five distinct reef communities [carbonate sand, crustose coralline algae (CCA), corals, fleshy algae, and a mixed community] under ambient and acidified conditions during summer and winter. The results showed that different communities had distinct influences on carbonate chemistry related to the relative importance of NCC and NCP. Sand, CCA, and corals exerted relatively small influences on <span class="hlt">seawater</span> pH and Ω a over diel cycles due to closely balanced NCC and NCP rates, whereas fleshy algae and mixed communities strongly elevated daytime pH and Ω a due to high NCP rates. Interestingly, the influence on <span class="hlt">seawater</span> pH at night was relatively small and quite similar across communities. NCC and NCP rates were not significantly affected by short-term acidification, but larger diel variability in pH was observed due to decreased <span class="hlt">seawater</span> buffering capacity. Except for corals, increased net dissolution was observed at night for all communities under OA, partially buffering against nighttime acidification. Thus, algal-dominated areas of coral reefs and increased</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1406714-investigations-reusability-amidoxime-based-polymeric-adsorbents-seawater-uranium-extraction','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1406714-investigations-reusability-amidoxime-based-polymeric-adsorbents-seawater-uranium-extraction"><span>Investigations into the Reusability of Amidoxime-Based Polymeric Adsorbents for <span class="hlt">Seawater</span> Uranium Extraction</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Kuo, Li-Jung; Pan, Horng-Bin; Wai, Chien M.</p> <p></p> <p>The ability to re-use amidoxime-based polymeric adsorbents is a critical component in reducing the overall cost of the technology to extract uranium from <span class="hlt">seawater</span>. This report describes an evaluation of adsorbent reusability in multiple re-use (adsorption/stripping) cycles in real <span class="hlt">seawater</span> exposures with potassium bicarbonate (KHCO3) elution using several amidoxime-based polymeric adsorbents. The KHCO3 elution technique achieved ~100% recovery of uranium adsorption capacity in the first re-use. Subsequent re-uses showed significant drops in adsorption capacity. After the 4th re-use with the ORNL AI8 adsorbent, the 56-day adsorption capacity dropped to 28% of its original capacity. FTIR spectra revealed that there wasmore » a conversion of the amidoxime ligands to carboxylate groups during extended <span class="hlt">seawater</span> exposure, becoming more significant with longer the exposure time. Ca and Mg adsorption capacities also increased with each re-use cycle supporting the hypothesis that long term exposure resulted in converting amidoxime to carboxylate, enhancing the adsorption of Ca and Mg. Shorter <span class="hlt">seawater</span> exposure (adsorption/stripping) cycles (28 vs. 42 days) had higher adsorption capacities after re-use, but the shorter exposure cycle time did not produce an overall better performance in terms of cumulative exposure time. Recovery of uranium capacity in re-uses may also vary across different adsorbent formulations. Through multiple re-use the adsorbent AI8 can harvest 10 g uranium/kg adsorbent in ~140 days, using a 28-day adsorption/stripping cycle, a performance much better than would be achieved with a single use of the adsorbent through very long-term exposure (saturation capacity = 7.4 g U/kg adsorbent). A time dependent <span class="hlt">seawater</span> exposure model to evaluate the cost associated with reusing amidoxime-based adsorbents in real <span class="hlt">seawater</span> exposures was developed. The cost to extract uranium from <span class="hlt">seawater</span> ranged from $610-830/kg U was predicted. Model simulation suggests that a</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/15726441','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/15726441"><span>Growth of Bacillus methanolicus in <span class="hlt">seawater</span>-based media.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Komives, Claire F; Cheung, Louis Yip-Yan; Pluschkell, Stefanie B; Flickinger, Michael C</p> <p>2005-02-01</p> <p>Bacillus methanolicus has been proposed as a biocatalyst for the low cost production of commodity chemicals. The organism can use methanol as sole carbon and energy source, and it grows aerobically at elevated temperatures. Methanol can be made available from off-shore conversion of natural gas to methanol, through gas-to-liquid technology. Growth of the organism in <span class="hlt">seawater</span>-based medium would further reduce the costs of chemical production performed near an off-shore natural gas source. The growth of strain PB1 (ATCC 51375) in shake flask experiments with trypticase soy broth medium showed minimal salt-inhibition at the concentration of NaCl in <span class="hlt">seawater</span>. The ability of B. methanolicus PB1 to grow in Pacific Ocean water using methanol as a carbon and energy source was also tested. Following a simple adaptation procedure, PB1 was able to grow on methanol in semi-defined medium with 100% <span class="hlt">seawater</span> with good growth yields and similar growth rates compared with those achieved on media prepared in deionized water.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4567045','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=4567045"><span>River-derived humic substances as iron chelators in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Krachler, Regina; Krachler, Rudolf F.; Wallner, Gabriele; Hann, Stephan; Laux, Monika; Cervantes Recalde, Maria F.; Jirsa, Franz; Neubauer, Elisabeth; von der Kammer, Frank; Hofmann, Thilo; Keppler, Bernhard K.</p> <p>2015-01-01</p> <p>The speciation of iron(III) in oxic <span class="hlt">seawater</span> is dominated by its hydrolysis and sedimentation of insoluble iron(III)-oxyhydroxide. As a consequence, many oceanic areas have very low iron levels in surface <span class="hlt">seawater</span> which leads to iron deficiency since phytoplankton require iron as a micronutrient in order to grow. Fortunately, iron solubility is not truly as low as Fe(III) solubility measurements in inorganic <span class="hlt">seawater</span> would suggest, since oceanic waters contain organic molecules which tend to bind the iron and keep it in solution. Various iron-binding organic ligands which combine to stabilize dissolved iron have been detected and thoroughly investigated in recent years. However, the role of iron-binding ligands from terrestrial sources remains poorly constrained. Blackwater rivers supply large amounts of natural organic material (NOM) to the ocean. This NOM (which consists mainly of vascular plant-derived humic substances) is able to greatly enhance iron bioavailability in estuaries and coastal regions, however, breakdown processes lead to a rapid decrease of river-derived NOM concentrations with increasing distance from land. It has therefore been argued that the influence of river-derived NOM on iron biogeochemistry in offshore <span class="hlt">seawater</span> does not seem to be significant. Here we used a standard method based on 59Fe as a radiotracer to study the solubility of Fe(III)-oxyhydroxide in <span class="hlt">seawater</span> in the presence of riverine NOM. We aimed to address the question how effective is freshwater NOM as an iron chelator under open ocean conditions where the concentration of land-derived organic material is about 3 orders of magnitude smaller than in coastal regions, and does this iron chelating ability vary between NOM from different sources and between different size fractions of the river-borne NOM. Our results show that the investigated NOM fractions were able to substantially enhance Fe(III)-oxyhydroxide solubility in <span class="hlt">seawater</span> at concentrations of the NOM ≥ 5</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012EGUGA..14.3174F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012EGUGA..14.3174F"><span>Validation and Interpretation of a new sea <span class="hlt">ice</span> Glob<span class="hlt">Ice</span> dataset using buoys and the CICE sea <span class="hlt">ice</span> model</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Flocco, D.; Laxon, S. W.; Feltham, D. L.; Haas, C.</p> <p>2012-04-01</p> <p>The Glob<span class="hlt">Ice</span> project has provided high resolution sea <span class="hlt">ice</span> product datasets over the Arctic derived from SAR data in the ESA archive. The products are validated sea <span class="hlt">ice</span> motion, deformation and fluxes through straits. Glob<span class="hlt">Ice</span> sea <span class="hlt">ice</span> velocities, deformation data and sea <span class="hlt">ice</span> concentration have been validated using buoy data provided by the International Arctic Buoy Program (IABP). Over 95% of the Glob<span class="hlt">Ice</span> and buoy data analysed fell within 5 km of each other. The Glob<span class="hlt">Ice</span> Eulerian image pair product showed a high correlation with buoy data. The sea <span class="hlt">ice</span> concentration product was compared to SSM/I data. An evaluation of the validity of the Glob<span class="hlt">ICE</span> data will be presented in this work. Glob<span class="hlt">ICE</span> sea <span class="hlt">ice</span> velocity and deformation were compared with runs of the CICE sea <span class="hlt">ice</span> model: in particular the mass fluxes through the straits were used to investigate the correlation between the winter behaviour of sea <span class="hlt">ice</span> and the sea <span class="hlt">ice</span> state in the following summer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1988SPIE..917...19J','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1988SPIE..917...19J"><span>Infrared Laser Optoacoustic Detection Of Gases And <span class="hlt">Vapours</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Johnson, S. A.; Cummins, P. G.; Bone, S. A.; Davies, P. B.</p> <p>1988-10-01</p> <p>Mid-infrared laser optoacoustic spectroscopy has been used to detect a variety of gases and <span class="hlt">vapours</span>. Performance was calibrated using the signal from a known concentration of ethene, and then the method applied to the perfume alcohol geraniol. Detection limits were found to be 1 ppb for ethene and 70 ppb for geraniol on their strongest absorption lines for a few seconds measurement time.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27686294','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27686294"><span>The effect of ethanol <span class="hlt">vapour</span> exposure on atrial and ventricular walls of chick embryos.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kamran, Kiran; Khan, Muhammad Yunus; Minhas, Liaqat Ali</p> <p>2016-10-01</p> <p>To study the effects of ethanol <span class="hlt">vapour</span> exposure on atrial and ventricular walls of heart in chick embryo. The study design was experimental, conducted at Islamabad Centre of College of Physicians and Surgeons, Pakistan. One hundred and eighty chicken eggs were divided into two groups, experimental and control, of 90 eggs each. Each group was subdivided into three subgroups of 30 eggs each based on the day of sacrifice. Experimental group was exposed to ethanol <span class="hlt">vapours</span> and then compared with age matched controls. The thickness of atrial and ventricular walls along with lengths of valvular cusps increased in hearts of day 7 and day 10 chick embryos in experimental group. There was thinning of walls and decreased length of valvular cusps in hearts of experimental chicks on hatching as compared to age matched controls. Ethanol <span class="hlt">vapour</span> exposure during development causes cardiac and septal wall thickening during initial days of development followed by cardiac and septal wall thinning which is a classical picture of alcohol induced cardiomyopathies.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/19970009633','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/19970009633"><span>Characterization of <span class="hlt">Ice</span> Roughness From Simulated <span class="hlt">Icing</span> Encounters</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Anderson, David N.; Shin, Jaiwon</p> <p>1997-01-01</p> <p>Detailed measurements of the size of roughness elements on <span class="hlt">ice</span> accreted on models in the NASA Lewis <span class="hlt">Icing</span> Research Tunnel (IRT) were made in a previous study. Only limited data from that study have been published, but included were the roughness element height, diameter and spacing. In the present study, the height and spacing data were found to correlate with the element diameter, and the diameter was found to be a function primarily of the non-dimensional parameters freezing fraction and accumulation parameter. The width of the smooth zone which forms at the leading edge of the model was found to decrease with increasing accumulation parameter. Although preliminary, the success of these correlations suggests that it may be possible to develop simple relationships between <span class="hlt">ice</span> roughness and <span class="hlt">icing</span> conditions for use in <span class="hlt">ice</span>-accretion-prediction codes. These codes now require an <span class="hlt">ice</span>-roughness estimate to determine convective heat transfer. Studies using a 7.6-cm-diameter cylinder and a 53.3-cm-chord NACA 0012 airfoil were also performed in which a 1/2-min <span class="hlt">icing</span> spray at an initial set of conditions was followed by a 9-1/2-min spray at a second set of conditions. The resulting <span class="hlt">ice</span> shape was compared with that from a full 10-min spray at the second set of conditions. The initial <span class="hlt">ice</span> accumulation appeared to have no effect on the final <span class="hlt">ice</span> shape. From this result, it would appear the accreting <span class="hlt">ice</span> is affected very little by the initial roughness or shape features.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C31D..06T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C31D..06T"><span>Submesoscale sea <span class="hlt">ice</span>-ocean interactions in marginal <span class="hlt">ice</span> zones</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Thompson, A. F.; Manucharyan, G.</p> <p>2017-12-01</p> <p>Signatures of ocean eddies, fronts and filaments are commonly observed within the marginal <span class="hlt">ice</span> zones (MIZ) from satellite images of sea <span class="hlt">ice</span> concentration, in situ observations via <span class="hlt">ice</span>-tethered profilers or under-<span class="hlt">ice</span> gliders. Localized and intermittent sea <span class="hlt">ice</span> heating and advection by ocean eddies are currently not accounted for in climate models and may contribute to their biases and errors in sea <span class="hlt">ice</span> forecasts. Here, we explore mechanical sea <span class="hlt">ice</span> interactions with underlying submesoscale ocean turbulence via a suite of numerical simulations. We demonstrate that the release of potential energy stored in meltwater fronts can lead to energetic submesoscale motions along MIZs with sizes O(10 km) and Rossby numbers O(1). In low-wind conditions, cyclonic eddies and filaments efficiently trap the sea <span class="hlt">ice</span> and advect it over warmer surface ocean waters where it can effectively melt. The horizontal eddy diffusivity of sea <span class="hlt">ice</span> mass and heat across the MIZ can reach O(200 m2 s-1). Submesoscale ocean variability also induces large vertical velocities (order of 10 m day-1) that can bring relatively warm subsurface waters into the mixed layer. The ocean-sea <span class="hlt">ice</span> heat fluxes are localized over cyclonic eddies and filaments reaching about 100 W m-2. We speculate that these submesoscale-driven intermittent fluxes of heat and sea <span class="hlt">ice</span> can potentially contribute to the seasonal evolution of MIZs. With continuing global warming and sea <span class="hlt">ice</span> thickness reduction in the Arctic Ocean, as well as the large expanse of thin sea <span class="hlt">ice</span> in the Southern Ocean, submesoscale sea <span class="hlt">ice</span>-ocean processes are expected to play a significant role in the climate system.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/9138000','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/9138000"><span>A study of ethylene glycol exposure and kidney function of aircraft de-<span class="hlt">icing</span> workers.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Gérin, M; Patrice, S; Bégin, D; Goldberg, M S; Vyskocil, A; Adib, G; Drolet, D; Viau, C</p> <p>1997-01-01</p> <p>Ethylene glycol levels were measured in 154 breathing zone air samples and in 117 urine samples of 33 aviation workers exposed to de-<span class="hlt">icing</span> fluid (basket operators, de-<span class="hlt">icing</span> truck drivers, leads and coordinators) studied during 42 worker-days over a winter period of 2 months at a Montreal airport. Ethylene glycol as <span class="hlt">vapour</span> did not exceed 22 mg/m3 (mean duration of samples 50 min). Mist was quantified at higher levels in 3 samples concerning 1 coordinator and 2 basket operators (76-190 mg/m3, 45-118 min). In 16 cases workers' post-shift or next-morning urine contained quantities of ethylene glycol exceeding 5 mmol/mol creatinine (up to 129 mmol/mol creatinine), with most of these instances occurring in basket operators and coordinators, some of whom did not wear paper masks and/or were accidentally sprayed with de-<span class="hlt">icing</span> fluid. Diethylene glycol was also found in a few air and urinary samples at levels around one tenth those of ethylene glycol. Urinary concentrations of albumin, beta-N-acetyl-glucosaminidase, beta-2-microglobulin and retinol-binding protein were measured and compared over various periods, according to subgroups based on exposure level and according to the frequency of extreme values. These analyses did not demonstrate acute or chronic kidney damage that could be attributed to working in the presence of ethylene glycol. In conclusion, this study does not suggest important health effects of exposure to de-<span class="hlt">icing</span> fluid in this group of workers. Potential for overexposure exists, however, in certain work situations, and recommendations on preventive measures are given. In addition, these results suggest that other routes of absorption than inhalation, such as the percutaneous route, may be important and that urinary ethylene glycol may be a useful indicator of exposure to ethylene glycol.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_20");'>20</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li class="active"><span>22</span></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_22 --> <div id="page_23" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="441"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-GSFC_20171208_Archive_e001932.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-GSFC_20171208_Archive_e001932.html"><span><span class="hlt">Ice</span> Stars</span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2017-12-08</p> <p><span class="hlt">Ice</span> Stars - August 4th, 2002 Description: Like distant galaxies amid clouds of interstellar dust, chunks of sea <span class="hlt">ice</span> drift through graceful swirls of grease <span class="hlt">ice</span> in the frigid waters of Foxe Basin near Baffin Island in the Canadian Arctic. Sea <span class="hlt">ice</span> often begins as grease <span class="hlt">ice</span>, a soupy slick of tiny <span class="hlt">ice</span> crystals on the ocean's surface. As the temperature drops, grease <span class="hlt">ice</span> thickens and coalesces into slabs of more solid <span class="hlt">ice</span>. Credit: USGS/NASA/Landsat 7 To learn more about the Landsat satellite go to: landsat.gsfc.nasa.gov/ NASA Goddard Space Flight Center enables NASA’s mission through four scientific endeavors: Earth Science, Heliophysics, Solar System Exploration, and Astrophysics. Goddard plays a leading role in NASA’s accomplishments by contributing compelling scientific knowledge to advance the Agency’s mission. Follow us on Twitter Join us on Facebook</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.A33M..02W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.A33M..02W"><span>Upper-Tropospheric Cloud <span class="hlt">Ice</span> from <span class="hlt">Ice</span>Cube</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Wu, D. L.</p> <p>2017-12-01</p> <p>Cloud <span class="hlt">ice</span> plays important roles in Earth's energy budget and cloud-precipitation processes. Knowledge of global cloud <span class="hlt">ice</span> and its properties is critical for understanding and quantifying its roles in Earth's atmospheric system. It remains a great challenge to measure these variables accurately from space. Submillimeter (submm) wave remote sensing has capability of penetrating clouds and measuring <span class="hlt">ice</span> mass and microphysical properties. In particular, the 883-GHz frequency is a highest spectral window in microwave frequencies that can be used to fill a sensitivity gap between thermal infrared (IR) and mm-wave sensors in current spaceborne cloud <span class="hlt">ice</span> observations. <span class="hlt">Ice</span>Cube is a cubesat spaceflight demonstration of 883-GHz radiometer technology. Its primary objective is to raise the technology readiness level (TRL) of 883-GHz cloud radiometer for future Earth science missions. By flying a commercial receiver on a 3U cubesat, <span class="hlt">Ice</span>Cube is able to achieve fast-track maturation of space technology, by completing its development, integration and testing in 2.5 years. <span class="hlt">Ice</span>Cube was successfully delivered to ISS in April 2017 and jettisoned from the International Space Station (ISS) in May 2017. The <span class="hlt">Ice</span>Cube cloud-<span class="hlt">ice</span> radiometer (ICIR) has been acquiring data since the jettison on a daytime-only operation. <span class="hlt">Ice</span>Cube adopted a simple design without payload mechanism. It makes maximum utilization of solar power by spinning the spacecraft continuously about the Sun vector at a rate of 1.2° per second. As a result, the ICIR is operated under the limited resources (8.6 W without heater) and largely-varying (18°C-28°C) thermal environments. The spinning cubesat also allows ICIR to have periodical views between the Earth (atmosphere and clouds) and cold space (calibration), from which the first 883-GHz cloud map is obtained. The 883-GHz cloud radiance, sensitive to <span class="hlt">ice</span> particle scattering, is proportional to cloud <span class="hlt">ice</span> amount above 10 km. The ICIR cloud map acquired during June 20-July 2</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008AGUFM.U42B..06E','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008AGUFM.U42B..06E"><span>Continental fragmentation and the strontium isotopic evolution of <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Eric, H.; Jean Pascal, C.</p> <p>2008-12-01</p> <p>The time evolution of the strontium isotopic composition of <span class="hlt">seawater</span> over the last 600 million years has the form of an asymmetric trough. The values are highest in the Cambrian and recent and lowest in the Jurassic. Superimposed on this trend are a number of smaller oscillations. The mechanisms responsible for these global isotopic fluctuations are subject to much debates. In order to get a quantitative picture of the changing paleogeography, we have characterized land-ocean distributions over Late Proterozoic to Phanerozoic times from measurement of perimeters and areas of continental fragments, based on paleomagnetic reconstructions. These measurements served to calculate geophysically constrainted breakup and scatter indexes of continental land masses from 0 to 1100 Ma (Cogne and Humler, 2008). Both parameters (strontium isotopic ratios of <span class="hlt">seawater</span> and continental fragmentation indexes) are obviously highly correlated during the last 600 Ma. Low continental dispersion (that is large continental land masses) are associated with low <span class="hlt">seawater</span> strontium isotopic ratios (that is when the continental inputs to oceans are minimum) and high continental dispersion (that is relatively small and widely distributed continents) with high <span class="hlt">seawater</span> strontium isotopic ratios (that is when the continental input to ocean is maximum). Importantly, this first order evolution appears to conflict with the common idea of mountains erosion as a source for radiogenic strontium to oceans because high strontium isotopic ratios in <span class="hlt">seawater</span> correspond to period of maximum dispersion of continents and not with period of general collisions. At first glance, it would seem that continental erosion increases with the degree of continental dispersion. Models showing that continental precipitation increases when continental masses are smaller and more widely dispersed and/or the length of continental margins available for rivers to carry continental material to oceans are thus favoured in order</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1255392-potential-impact-seawater-uranium-extraction-marine-life','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1255392-potential-impact-seawater-uranium-extraction-marine-life"><span>Potential impact of <span class="hlt">seawater</span> uranium extraction on marine life</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Park, Jiyeon; Jeters, Robert T.; Kuo, Li-Jung</p> <p></p> <p>A variety of adsorbent materials have been developed to extract uranium from <span class="hlt">seawater</span> as an alternative traditional terrestrial mining. A large-scale deployment of these adsorbents would be necessary to recover useful quantities of uranium and this raises a number of concerns regarding potential impacts on the surrounding marine environment. Two concerns are whether or not the adsorbent materials are toxic and any potentially harmful effects that may result from depleting uranium or vanadium (also highly concentrated by the adsorbents) from the local environment. To test the potential toxicity of the adsorbent with or without bound metals, Microtox assays were usedmore » to test both direct contact toxicity and the toxicity of any leachate in the <span class="hlt">seawater</span>. The Microtox assay was chosen because it the detection of non-specific mechanisms of toxicity. Toxicity was not observed with leachates from any of 68 adsorbent materials that were tested, but direct contact with some adsorbents at very high adsorbent con-centrations exhibited toxicity. These concentrations are, however, very unlikely to be seen in the actual marine deployment. Adsor-bents that accumulated uranium and trace metals were also tested for toxicity, and no toxic effect was observed. Biofouling on the adsorbents and in columns or flumes containing the adsorbents also indicates that the adsorbents are not toxic and that there may not be an obvious deleterious effect resulting from removing uranium and vanadium from <span class="hlt">seawater</span>. An extensive literature search was also performed to examine the potential impact of uranium and vanadium extraction from <span class="hlt">seawater</span> on marine life using the Pacific Northwest National Laboratory’s (PNNL’s) document analysis tool, IN-SPIRE™. Although other potential environmental effects must also be considered, results from both the Microtox assay and the literature search provide preliminary evidence that uranium extraction from <span class="hlt">seawater</span> could be performed with minimal</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5760964','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5760964"><span>Thermally decarboxylated sodium bicarbonate: Interactions with water <span class="hlt">vapour</span>, calorimetric study</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Volkova, Natalia; Hansson, Henri; Ljunggren, Lennart</p> <p>2012-01-01</p> <p>Isothermal titration calorimetry (ITC) was used to study interactions between water <span class="hlt">vapour</span> and the surface of thermally converted sodium bicarbonate (NaHCO3). The decarboxylation degree of the samples was varied from 3% to 35% and the humidity range was 54–100%. The obtained enthalpy values were all exothermic and showed a positive linear correlation with decarboxylation degrees for each humidity studied. The critical humidity, 75% (RHo), was determined as the inflection point on a plot of the mean−ΔH kJ/mole Na2CO3 against RH. Humidities above the critical humidity lead to complete surface dissolution. The water uptake (m) was determined after each calorimetric experiment, complementing the enthalpy data. A mechanism of water <span class="hlt">vapour</span> interaction with decarboxylated samples, including the formation of trona and Wegscheider’s salt on the bicarbonate surface is proposed for humidities below RHo. PMID:29403816</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017TCry...11.2543S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017TCry...11.2543S"><span><span class="hlt">Ice</span> shelf fracture parameterization in an <span class="hlt">ice</span> sheet model</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Sun, Sainan; Cornford, Stephen L.; Moore, John C.; Gladstone, Rupert; Zhao, Liyun</p> <p>2017-11-01</p> <p>Floating <span class="hlt">ice</span> shelves exert a stabilizing force onto the inland <span class="hlt">ice</span> sheet. However, this buttressing effect is diminished by the fracture process, which on large scales effectively softens the <span class="hlt">ice</span>, accelerating its flow, increasing calving, and potentially leading to <span class="hlt">ice</span> shelf breakup. We add a continuum damage model (CDM) to the BISICLES <span class="hlt">ice</span> sheet model, which is intended to model the localized opening of crevasses under stress, the transport of those crevasses through the <span class="hlt">ice</span> sheet, and the coupling between crevasse depth and the <span class="hlt">ice</span> flow field and to carry out idealized numerical experiments examining the broad impact on large-scale <span class="hlt">ice</span> sheet and shelf dynamics. In each case we see a complex pattern of damage evolve over time, with an eventual loss of buttressing approximately equivalent to halving the thickness of the <span class="hlt">ice</span> shelf. We find that it is possible to achieve a similar <span class="hlt">ice</span> flow pattern using a simple rule of thumb: introducing an enhancement factor ˜ 10 everywhere in the model domain. However, spatially varying damage (or equivalently, enhancement factor) fields set at the start of prognostic calculations to match velocity observations, as is widely done in <span class="hlt">ice</span> sheet simulations, ought to evolve in time, or grounding line retreat can be slowed by an order of magnitude.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22750870','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22750870"><span>Crystallization and preliminary X-ray crystallographic analysis of an <span class="hlt">ice</span>-binding protein (FfIBP) from Flavobacterium frigoris PS1.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Do, Hackwon; Lee, Jun Hyuck; Lee, Sung Gu; Kim, Hak Jun</p> <p>2012-07-01</p> <p><span class="hlt">Ice</span> growth in a cold environment is fatal for polar organisms, not only because of the physical destruction of inner cell organelles but also because of the resulting chemical damage owing to processes such as osmotic shock. The properties of <span class="hlt">ice</span>-binding proteins (IBPs), which include antifreeze proteins (AFPs), have been characterized and IBPs exhibit the ability to inhibit <span class="hlt">ice</span> growth by binding to specific <span class="hlt">ice</span> planes and lowering the freezing point. An <span class="hlt">ice</span>-binding protein (FfIBP) from the Gram-negative bacterium Flavobacterium frigoris PS1, which was isolated from the Antarctic, has recently been overexpressed. Interestingly, the thermal hysteresis activity of FfIBP was approximately 2.5 K at 50 µM, which is ten times higher than that of the moderately active IBP from Arctic yeast (LeIBP). Although FfIBP closely resembles LeIBP in its amino-acid sequence, the antifreeze activity of FfIBP appears to be much greater than that of LeIBP. In an effort to understand the reason for this difference, an attempt was made to solve the crystal structure of FfIBP. Here, the crystallization and X-ray diffraction data of FfIBP are reported. FfIBP was crystallized using the hanging-drop <span class="hlt">vapour</span>-diffusion method with 0.1 M sodium acetate pH 4.4 and 3 M sodium chloride as precipitant. A complete diffraction data set was collected to a resolution of 2.9 Å. The crystal belonged to space group P4(1)22, with unit-cell parameters a = b = 69.4, c = 178.2 Å. The asymmetric unit contained one monomer.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013ChJOL..31..860F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013ChJOL..31..860F"><span>Henry's law constant for phosphine in <span class="hlt">seawater</span>: determination and assessment of influencing factors</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fu, Mei; Yu, Zhiming; Lu, Guangyuan; Song, Xiuxian</p> <p>2013-07-01</p> <p>The Henry's Law constant ( k) for phosphine in <span class="hlt">seawater</span> was determined by multiple phase equilibration combined with headspace gas chromatography. The effects of pH, temperature, and salinity on k were studied. The k value for phosphine in natural <span class="hlt">seawater</span> was 6.415 at room temperature (approximately 23°C). This value increases with increases in temperature and salinity, but no obvious change was observed at different pH levels. At the same temperature, there was no significant difference between the k for phosphine in natural <span class="hlt">seawater</span> and that in artificial <span class="hlt">seawater</span>. This implies that temperature and salinity are major determining factors for k in marine environment. Double linear regression with Henry's Law constants for phosphine as a function of temperature and salinity confirmed our observations. These results provide a basis for the measurement of trace phosphine concentrations in <span class="hlt">seawater</span>, and will be helpful for future research on the status of phosphine in the oceanic biogeochemical cycle of phosphorus.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/1255367-nanostructured-metal-oxide-sorbents-collection-recovery-uranium-from-seawater','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/1255367-nanostructured-metal-oxide-sorbents-collection-recovery-uranium-from-seawater"><span>Nanostructured Metal Oxide Sorbents for the Collection and Recovery of Uranium from <span class="hlt">Seawater</span></span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Chouyyok, Wilaiwan; Warner, Cynthia L.; Mackie, Katherine E.</p> <p>2016-02-07</p> <p>The ability to collect uranium from <span class="hlt">seawater</span> offers the potential for a long-term green fuel supply for nuclear energy. However, extraction of uranium, and other trace minerals, is challenging due to the high ionic strength and low mineral concentrations in <span class="hlt">seawater</span>. Herein we evaluate the use of nanostructured metal oxide sorbents for the collection and recovery of uranium from <span class="hlt">seawater</span>. Chemical affinity, chemical adsorption capacity and kinetics of preferred sorbent materials were evaluated. High surface area manganese and iron oxide nanomaterials showed excellent performance for uranium collection from <span class="hlt">seawater</span>. Inexpensive nontoxic carbonate solutions were demonstrated to be an effective andmore » environmental benign method of stripping the uranium from the metal oxide sorbents. Various formats for the utilization of the nanostructured metals oxide sorbent materials are discussed including traditional and nontraditional methods such as magnetic separation. Keywords: Uranium, nano, manganese, iron, sorbent, <span class="hlt">seawater</span>, magnetic, separations, nuclear energy« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27345708','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27345708"><span>Effect of phytoplankton biomass in <span class="hlt">seawater</span> on chemical properties of sea spray aerosols.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Park, Jiyeon; Kim, Dohyung; Lee, Kwangyul; Han, Seunghee; Kim, Hyunji; Williams, Leah R; Joo, Hung Soo; Park, Kihong</p> <p>2016-09-15</p> <p>This study is to investigate the effect of biological <span class="hlt">seawater</span> properties on sea spray aerosols (SSA). Concentrations of chlorophyll-a and bacteria were measured at coastal site in Korea in fall and summer seasons. Also, aerosol mass spectrometer (AMS) was used to determine chemical constituents (organics, sulfate, nitrate, ammonium, and chloride) of non-refractory submicrometer aerosols sprayed from <span class="hlt">seawaters</span> using a bubble bursting system. The average concentration of chlorophyll-a in <span class="hlt">seawater</span> in fall was 1.75±0.78μg/l, whereas it significantly increased to 5.11±2.16μg/l in summer. It was found that the fraction of organics in the submicrometer SSA was higher in summer (68%) than fall (49%), and that the organic fraction in the SSA increased as the concentration of chlorophyll-a increased in <span class="hlt">seawater</span>, suggesting that the high phytoplankton biomass in <span class="hlt">seawater</span> could lead to the enhancement of organic species in the SSA. Copyright © 2016 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/28598345','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/28598345"><span>Microbiological quality of <span class="hlt">ice</span> and <span class="hlt">ice</span> machines used in food establishments.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Hampikyan, Hamparsun; Bingol, Enver Baris; Cetin, Omer; Colak, Hilal</p> <p>2017-06-01</p> <p>The <span class="hlt">ice</span> used in the food industry has to be safe and the water used in <span class="hlt">ice</span> production should have the quality of drinking water. The consumption of contaminated <span class="hlt">ice</span> directly or indirectly may be a vehicle for transmission of pathogenic bacteria to humans producing outbreaks of gastrointestinal diseases. The objective of this study was to monitor the microbiological quality of <span class="hlt">ice</span>, the water used in producing <span class="hlt">ice</span> and the hygienic conditions of <span class="hlt">ice</span> making machines in various food enterprises. Escherichia coli was detected in seven (6.7%) <span class="hlt">ice</span> and 23 (21.9%) <span class="hlt">ice</span> chest samples whereas E. coli was negative in all examined water samples. Psychrophilic bacteria were detected in 83 (79.0%) of 105 <span class="hlt">ice</span> chest and in 68 (64.7%) of 105 <span class="hlt">ice</span> samples, whereas Enterococci were detected only in 13 (12.4%) <span class="hlt">ice</span> samples. Coliforms were detected in 13 (12.4%) water, 71 (67.6%) <span class="hlt">ice</span> chest and 54 (51.4%) <span class="hlt">ice</span> samples. In order to improve the microbiological quality of <span class="hlt">ice</span>, the maintenance, cleaning and disinfecting of <span class="hlt">ice</span> machines should be carried out effectively and periodically. Also, high quality water should be used for <span class="hlt">ice</span> production.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C34B..02B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C34B..02B"><span>Constraining <span class="hlt">ice</span> sheet history in the Weddell Sea, West Antarctica, using <span class="hlt">ice</span> fabric at Korff <span class="hlt">Ice</span> Rise</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Brisbourne, A.; Smith, A.; Kendall, J. M.; Baird, A. F.; Martin, C.; Kingslake, J.</p> <p>2017-12-01</p> <p>The grounding history of <span class="hlt">ice</span> rises (grounded area of independent flow regime within a floating <span class="hlt">ice</span> shelf) can be used to constrain large scale <span class="hlt">ice</span> sheet history: <span class="hlt">ice</span> fabric, resulting from the preferred orientation of <span class="hlt">ice</span> crystals due to the stress regime, can be used to infer this grounding history. With the aim of measuring the present day <span class="hlt">ice</span> fabric at Korff <span class="hlt">Ice</span> Rise, West Antarctica, a multi-azimuth wide-angle seismic experiment was undertaken. Three wide-angle common-midpoint gathers were acquired centred on the apex of the <span class="hlt">ice</span> rise, at azimuths of 60 degrees to one another, to measure variation in seismic properties with offset and azimuth. Both vertical and horizontal receivers were used to record P and S arrivals including converted phases. Measurements of the variation with offset and azimuth of seismic traveltimes, seismic attenuation and shear wave splitting have been used to quantify seismic anisotropy in the <span class="hlt">ice</span> column. The observations cannot be reproduced using an isotropic <span class="hlt">ice</span> column model. Anisotropic ray tracing has been used to test likely models of <span class="hlt">ice</span> fabric by comparison with the data. A model with a weak girdle fabric overlying a strong cluster fabric provides the best fit to the observations. Fabric of this nature is consistent with Korff <span class="hlt">Ice</span> Rise having been stable for the order of 10,000 years without any ungrounding or significant change in the <span class="hlt">ice</span> flow configuration across the <span class="hlt">ice</span> rise for this period. This observation has significant implications for the <span class="hlt">ice</span> sheet history of the Weddell Sea sector.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26447943','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26447943"><span>Lithium sorption properties of HMnO in <span class="hlt">seawater</span> and wastewater.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Park, HyunJu; Singhal, Naresh; Jho, Eun Hea</p> <p>2015-12-15</p> <p>The lithium concentration in <span class="hlt">seawater</span> is 0.17 mg/L, which is very low, but the overall quantity is approximately 2.5 × 10(14) kg. Therefore, <span class="hlt">seawater</span>, which contains a vast amount of lithium, could be a major alternative source that might supply the rising demand for lithium. This research was undertaken to evaluate the feasibility of a manganese oxide (HMnO) adsorbent, which was produced after leaching lithium from lithium manganese oxide, for lithium collection from <span class="hlt">seawater</span>. The HMnO was synthesized and deformed to a plastic after wet blending of manganese oxide and lithium hydroxide, and subsequently, the influence of pH, sorption isotherms, sorption rates, sorption energies, and effects of the co-ions were measured. Thermodynamic parameters such as ΔG°, ΔH°, and ΔS° indicated that the nature of the lithium sorption was both spontaneous and endothermic. The used HMnO could be regenerated by washing it with an HCl solution. The results demonstrated that HMnO could be effectively used for the collection of lithium from <span class="hlt">seawater</span> with good selectivity. Copyright © 2015 Elsevier Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012JPhD...45t5202L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012JPhD...45t5202L"><span>Measurement of the densities of Cu and Ag <span class="hlt">vapours</span> in a low-voltage switch using the hook method</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lins, Günter</p> <p>2012-05-01</p> <p>In a research model of a low-voltage circuit breaker with fixed contacts and windows for optical access, arcs powered by either a high-current transformer or a capacitor bank were initiated by the explosion of tungsten wires. Air at atmospheric pressure was the switching medium. The number densities of neutral silver and copper <span class="hlt">vapours</span> from contacts and arc runners were measured simultaneously by the hook method using a Mach-Zehnder interferometer combined with a 1 m spectrograph and a gated intensified CCD camera. When an arc current was flowing, a substantial fraction of the metal <span class="hlt">vapour</span> was ionized, and thus not amenable to a density measurement with the technique chosen. To nevertheless obtain approximate density values, the arc current was forced to zero within 8 to 10 µs at a preset time and measurements were carried out 100 µs after extinction of the arc. At that time the metal <span class="hlt">vapour</span> was expected to have recombined to a large extent but not yet diffused to the walls in significant amounts. Depending on the current amplitude reached within the arc duration the arc remained anchored to the silver contacts or commutated to the copper arc runners. At a maximum current amplitude of 650 A Ag <span class="hlt">vapour</span> densities of the order of 1022 m-3 were observed near the anode outweighing the Cu <span class="hlt">vapour</span> density by a factor of 20. When at 1600 A the arc commutated to the arc runners a Cu <span class="hlt">vapour</span> density of 8 × 1021 m-3 was reached while the Ag density remained limited to 2 × 1021 m-3.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.7771Y','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.7771Y"><span>Hydrochemical and isotopic characteristics of estuarial <span class="hlt">seawater</span> and river water of Bailanghe in Laizhou Bay, China</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Yang, Qiaofeng; Xu, Suning; Wang, Ruijiu; Li, Wenpeng; Wang, Zhiyi; Mei, Junjun; Ding, Zhilei; Yang, Peijie; Yu, Liangju; Lv, Tieying; Bai, Gang; Kang, Wei</p> <p>2016-04-01</p> <p>In the study of <span class="hlt">seawater</span> intrusion, <span class="hlt">seawater</span> is usually taken as an end-member that mixes with other source(s). However, compared to standard <span class="hlt">seawater</span>, the coastal <span class="hlt">seawater</span> particularly that near the estuary, can be strongly influenced by the rivers into the sea and by coastal human activities. Their composition can be thus continuously changed and redistributed with space and time. Therefore, before investigating <span class="hlt">seawater</span> intrusion in a certain area, it is essentially important to determine the features of the estuarine <span class="hlt">seawater</span> (e.g. the mixture percentage between standard <span class="hlt">seawater</span> and river water). In this study, we aimed to gain a clear situation of the <span class="hlt">seawater</span> intrusion in Laizhou Bay, Southern Bohai, China. The issue aforementioned was investigated by comparing the stable isotopic and hydrochemical composition of the marine and river water collected in this area. Samples investigated include 5 surface water samples collected at the downstream of the Bailanghe and 7 <span class="hlt">seawater</span> samples near the estuary of Laizhou Bay. Inert tracers (δD, δ18O, Cl, Br) and reaction tracers (Na, Mg, SO4, HCO3, Ca, NO3) are particularly analyzed. The major results are as follows: 1) All the river water samples fall below the Global Meteoric Water Line in the δD - δ18O diagram, reflecting evaporation of the upstream reservoir water. The <span class="hlt">seawater</span> samples fall on the mixing line of standard <span class="hlt">seawater</span> and the river water in the stable isotopic diagram. 2) The Cl-δ18O diagram indicates widespread dissolution of evaporate into the river, while high concentration of Ca and HCO3-, as well as the SO42- - Cl relation of the river water samples reflect the dissolution of CO2 , carbonate and sulfate in the atmosphere and on the ground. 3) The Br/Cl ratios of <span class="hlt">seawater</span> samples are closed to the marine ratios. This together with the plots of major ions vs. Cl suggest that the <span class="hlt">seawater</span> samples are originated from the mixture of standard <span class="hlt">seawater</span> and river water. Therefore, when referring to the</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/27750163','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/27750163"><span>Capillary microextraction: A new method for sampling methamphetamine <span class="hlt">vapour</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Nair, M V; Miskelly, G M</p> <p>2016-11-01</p> <p>Clandestine laboratories pose a serious health risk to first responders, investigators, decontamination companies, and the public who may be inadvertently exposed to methamphetamine and other chemicals used in its manufacture. Therefore there is an urgent need for reliable methods to detect and measure methamphetamine at such sites. The most common method for determining methamphetamine contamination at former clandestine laboratory sites is selected surface wipe sampling, followed by analysis with gas chromatography-mass spectrometry (GC-MS). We are investigating the use of sampling for methamphetamine <span class="hlt">vapour</span> to complement such wipe sampling. In this study, we report the use of capillary microextraction (CME) devices for sampling airborne methamphetamine, and compare their sampling efficiency with a previously reported dynamic SPME method. The CME devices consisted of PDMS-coated glass filter strips inside a glass tube. The devices were used to dynamically sample methamphetamine <span class="hlt">vapour</span> in the range of 0.42-4.2μgm -3 , generated by a custom-built <span class="hlt">vapour</span> dosing system, for 1-15min, and methamphetamine was analysed using a GC-MS fitted with a ChromatoProbe thermal desorption unit. The devices showed good reproducibility (RSD<15%), and a curvilinear pre-equilibrium relationship between sampling times and peak area, which can be utilised for calibration. Under identical sampling conditions, the CME devices were approximately 30 times more sensitive than the dynamic SPME method. The CME devices could be stored for up to 3days after sampling prior to analysis. Consecutive sampling of methamphetamine and its isotopic substitute, d-9 methamphetamine showed no competitive displacement. This suggests that CME devices, pre-loaded with an internal standard, could be a feasible method for sampling airborne methamphetamine at former clandestine laboratories. Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2015GeCoA.170...51S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2015GeCoA.170...51S"><span>A novel determination of calcite dissolution kinetics in <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Subhas, Adam V.; Rollins, Nick E.; Berelson, William M.; Dong, Sijia; Erez, Jonathan; Adkins, Jess F.</p> <p>2015-12-01</p> <p>We present a novel determination of the dissolution kinetics of inorganic calcite in <span class="hlt">seawater</span>. We dissolved 13 C -labeled calcite in unlabeled <span class="hlt">seawater</span>, and traced the evolving δ13 C composition of the fluid over time to establish dissolution rates. This method provides sensitive determinations of dissolution rate, which we couple with tight constraints on both <span class="hlt">seawater</span> saturation state and surface area of the dissolving minerals. We have determined dissolution rates for two different abiotic calcite materials and three different grain sizes. Near-equilibrium dissolution rates are highly nonlinear, and are well normalized by geometric surface area, giving an empirical dissolution rate dependence on saturation state (Ω) of: This result substantiates the non-linear response of calcite dissolution to undersaturation. The bulk dissolution rate constant calculated here is in excellent agreement with those determined in far from equilibrium and dilute solution experiments. Plots of dissolution versus undersaturation indicates the presence of at least two dissolution mechanisms, implying a criticality in the calcite-<span class="hlt">seawater</span> system. Finally, our new rate determination has implications for modeling of pelagic and seafloor dissolution. Nonlinear dissolution kinetics in a simple 1-D lysocline model indicate a possible transition from kinetic to diffusive control with increasing water depth, and also confirm the importance of respiration-driven dissolution in setting the shape of the calcite lysocline.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017JGRC..122.9455M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017JGRC..122.9455M"><span>Submesoscale Sea <span class="hlt">Ice</span>-Ocean Interactions in Marginal <span class="hlt">Ice</span> Zones</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Manucharyan, Georgy E.; Thompson, Andrew F.</p> <p>2017-12-01</p> <p>Signatures of ocean eddies, fronts, and filaments are commonly observed within marginal <span class="hlt">ice</span> zones (MIZs) from satellite images of sea <span class="hlt">ice</span> concentration, and in situ observations via <span class="hlt">ice</span>-tethered profilers or underice gliders. However, localized and intermittent sea <span class="hlt">ice</span> heating and advection by ocean eddies are currently not accounted for in climate models and may contribute to their biases and errors in sea <span class="hlt">ice</span> forecasts. Here, we explore mechanical sea <span class="hlt">ice</span> interactions with underlying submesoscale ocean turbulence. We demonstrate that the release of potential energy stored in meltwater fronts can lead to energetic submesoscale motions along MIZs with spatial scales O(10 km) and Rossby numbers O(1). In low-wind conditions, cyclonic eddies and filaments efficiently trap the sea <span class="hlt">ice</span> and advect it over warmer surface ocean waters where it can effectively melt. The horizontal eddy diffusivity of sea <span class="hlt">ice</span> mass and heat across the MIZ can reach O(200 m2 s-1). Submesoscale ocean variability also induces large vertical velocities (order 10 m d-1) that can bring relatively warm subsurface waters into the mixed layer. The ocean-sea <span class="hlt">ice</span> heat fluxes are localized over cyclonic eddies and filaments reaching about 100 W m-2. We speculate that these submesoscale-driven intermittent fluxes of heat and sea <span class="hlt">ice</span> can contribute to the seasonal evolution of MIZs. With the continuing global warming and sea <span class="hlt">ice</span> thickness reduction in the Arctic Ocean, submesoscale sea <span class="hlt">ice</span>-ocean processes are expected to become increasingly prominent.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1983JCrGr..61..275F','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1983JCrGr..61..275F"><span><span class="hlt">Vapour</span> growth of argyrodite-type ionic conductors Cu 6PS 5Hal</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Fiechter, S.; Eckstein, J.; Nitsche, R.</p> <p>1983-03-01</p> <p>Cu 6PS 5Hal compounds (with Hal = Cl, Br or I) have been crystallized around 950 K by CVT with P, S and Hal (and combinations thereof). Chemical insight into the transport processes was gained from dissociation pressure measurements and spectroscopic <span class="hlt">vapour</span> analysis. Lacking thermochemical data of the compounds were obtained from Cp measurements. Models, derived for the CVT mechanisms, yield transport rates and directions which agree qualitatively with experiments. The main <span class="hlt">vapour</span> species (for Hal = C1) are PSCI 3, S 2, PCI 3, P 4S 3 and (CuCl) 3. With a surplus of CuHal, VLS growth via liquid CuHal/Cu 2S phases was observed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=faraday&id=EJ930442','ERIC'); return false;" href="https://eric.ed.gov/?q=faraday&id=EJ930442"><span>Faraday's Law and <span class="hlt">Seawater</span> Motion</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>De Luca, R.</p> <p>2010-01-01</p> <p>Using Faraday's law, one can illustrate how an electromotive force generator, directly utilizing <span class="hlt">seawater</span> motion, works. The conceptual device proposed is rather simple in its components and can be built in any high school or college laboratory. The description of the way in which the device generates an electromotive force can be instructive not…</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li class="active"><span>23</span></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_23 --> <div id="page_24" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="461"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/24942000','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/24942000"><span>Variable response of three Trifolium repens ecotypes to soil flooding by <span class="hlt">seawater</span>.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>White, Anissia C; Colmer, Timothy D; Cawthray, Greg R; Hanley, Mick E</p> <p>2014-08-01</p> <p>Despite concerns about the impact of rising sea levels and storm surge events on coastal ecosystems, there is remarkably little information on the response of terrestrial coastal plant species to <span class="hlt">seawater</span> inundation. The aim of this study was to elucidate responses of a glycophyte (white clover, Trifolium repens) to short-duration soil flooding by <span class="hlt">seawater</span> and recovery following leaching of salts. Using plants cultivated from parent ecotypes collected from a natural soil salinity gradient, the impact of short-duration <span class="hlt">seawater</span> soil flooding (8 or 24 h) on short-term changes in leaf salt ion and organic solute concentrations was examined, together with longer term impacts on plant growth (stolon elongation) and flowering. There was substantial Cl(-) and Na(+) accumulation in leaves, especially for plants subjected to 24 h soil flooding with <span class="hlt">seawater</span>, but no consistent variation linked to parent plant provenance. Proline and sucrose concentrations also increased in plants following <span class="hlt">seawater</span> flooding of the soil. Plant growth and flowering were reduced by longer soil immersion times (<span class="hlt">seawater</span> flooding followed by drainage and freshwater inputs), but plants originating from more saline soil responded less negatively than those from lower salinity soil. The accumulation of proline and sucrose indicates a potential for solute accumulation as a response to the osmotic imbalance caused by salt ions, while variation in growth and flowering responses between ecotypes points to a natural adaptive capacity for tolerance of short-duration <span class="hlt">seawater</span> soil flooding in T. repens. Consequently, it is suggested that selection for tolerant ecotypes is possible should the predicted increase in frequency of storm surge flooding events occur. © The Author 2014. Published by Oxford University Press on behalf of the Annals of Botany Company. All rights reserved. For Permissions, please email: journals.permissions@oup.com.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19251995','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19251995"><span><span class="hlt">Seawater</span> Ca2+ concentration influences solar orientation in Talitrus saltator (Crustacea, Amphipoda).</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Ugolini, Alberto; Ungherese, Giuseppe; Mercatelli, Luca; Saer, Doumett; Lepri, Luciano</p> <p>2009-03-01</p> <p>The role of salinity in the ecophysiology of many intertidal invertebrates has been extensively investigated. Calcium (Ca(2+)), magnesium (Mg(2+)), potassium (K(+)) and sodium (Na(+)) are the major constituents of <span class="hlt">seawater</span> and it has been demonstrated that sandhoppers tested under the sun in diluted <span class="hlt">seawater</span> (3.5 per thousand) head seaward, instead of going landward as expected. Therefore, the variation in <span class="hlt">seawater</span> salinity (from 35 per thousand to 3.5 per thousand) influences their directional choice. This paper investigates the contribution of different cations to the sea-land directional choice of Talitrus saltator (Crustacea, Amphipoda) by the sun compass orientation mechanism. Results of releases carried out in basic <span class="hlt">seawater</span> selectively deprived of Ca(2+), Mg(2+) or K(+) and containing the same concentration of Na(+) indicate that only the reduction in Ca(2+) concentration affects the capacity of solar orientation. The pH does not influence the directional choice of sandhoppers and nor do small variations in salinity in the range 32-39 per thousand. Moreover, the clear photopositive tendency registered in experiments of phototaxis in Ca(2+)-deprived <span class="hlt">seawater</span> indicates that the absence of Ca(2+) does not affect the normal functioning of the visual cells. Therefore, our results show that Ca(2+) <span class="hlt">seawater</span> concentration is important for the correct functioning of one of the principal mechanisms of orientation in supralittoral amphipods and it could affect their survival in the field.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20140003875','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20140003875"><span>Modeling Commercial Turbofan Engine <span class="hlt">Icing</span> Risk With <span class="hlt">Ice</span> Crystal Ingestion</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Jorgenson, Philip C. E.; Veres, Joseph P.</p> <p>2013-01-01</p> <p>The occurrence of <span class="hlt">ice</span> accretion within commercial high bypass aircraft turbine engines has been reported under certain atmospheric conditions. Engine anomalies have taken place at high altitudes that have been attributed to <span class="hlt">ice</span> crystal ingestion, partially melting, and <span class="hlt">ice</span> accretion on the compression system components. The result was degraded engine performance, and one or more of the following: loss of thrust control (roll back), compressor surge or stall, and flameout of the combustor. As <span class="hlt">ice</span> crystals are ingested into the fan and low pressure compression system, the increase in air temperature causes a portion of the <span class="hlt">ice</span> crystals to melt. It is hypothesized that this allows the <span class="hlt">ice</span>-water mixture to cover the metal surfaces of the compressor stationary components which leads to <span class="hlt">ice</span> accretion through evaporative cooling. <span class="hlt">Ice</span> accretion causes a blockage which subsequently results in the deterioration in performance of the compressor and engine. The focus of this research is to apply an engine <span class="hlt">icing</span> computational tool to simulate the flow through a turbofan engine and assess the risk of <span class="hlt">ice</span> accretion. The tool is comprised of an engine system thermodynamic cycle code, a compressor flow analysis code, and an <span class="hlt">ice</span> particle melt code that has the capability of determining the rate of sublimation, melting, and evaporation through the compressor flow path, without modeling the actual <span class="hlt">ice</span> accretion. A commercial turbofan engine which has previously experienced <span class="hlt">icing</span> events during operation in a high altitude <span class="hlt">ice</span> crystal environment has been tested in the Propulsion Systems Laboratory (PSL) altitude test facility at NASA Glenn Research Center. The PSL has the capability to produce a continuous <span class="hlt">ice</span> cloud which are ingested by the engine during operation over a range of altitude conditions. The PSL test results confirmed that there was <span class="hlt">ice</span> accretion in the engine due to <span class="hlt">ice</span> crystal ingestion, at the same simulated altitude operating conditions as experienced previously in</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://ntrs.nasa.gov/search.jsp?R=19930061882&hterms=marginal&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D10%26Ntt%3Dmarginal','NASA-TRS'); return false;" href="https://ntrs.nasa.gov/search.jsp?R=19930061882&hterms=marginal&qs=Ntx%3Dmode%2Bmatchall%26Ntk%3DAll%26N%3D0%26No%3D10%26Ntt%3Dmarginal"><span>Wave effects on ocean-<span class="hlt">ice</span> interaction in the marginal <span class="hlt">ice</span> zone</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Liu, Antony K.; Hakkinen, Sirpa; Peng, Chih Y.</p> <p>1993-01-01</p> <p>The effects of wave train on <span class="hlt">ice</span>-ocean interaction in the marginal <span class="hlt">ice</span> zone are studied through numerical modeling. A coupled two-dimensional <span class="hlt">ice</span>-ocean model has been developed to include wave effects and wind stress for the predictions of <span class="hlt">ice</span> edge dynamics. The sea <span class="hlt">ice</span> model is coupled to the reduced-gravity ocean model through interfacial stresses. The main dynamic balance in the <span class="hlt">ice</span> momentum is between water-<span class="hlt">ice</span> stress, wind stress, and wave radiation stresses. By considering the exchange of momentum between waves and <span class="hlt">ice</span> pack through radiation stress for decaying waves, a parametric study of the effects of wave stress and wind stress on <span class="hlt">ice</span> edge dynamics has been performed. The numerical results show significant effects from wave action. The <span class="hlt">ice</span> edge is sharper, and <span class="hlt">ice</span> edge meanders form in the marginal <span class="hlt">ice</span> zone owing to forcing by wave action and refraction of swell system after a couple of days. Upwelling at the <span class="hlt">ice</span> edge and eddy formation can be enhanced by the nonlinear effects of wave action; wave action sharpens the <span class="hlt">ice</span> edge and can produce <span class="hlt">ice</span> meandering, which enhances local Ekman pumping and pycnocline anomalies. The resulting <span class="hlt">ice</span> concentration, pycnocline changes, and flow velocity field are shown to be consistent with previous observations.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2018BGeo...15.3169G','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2018BGeo...15.3169G"><span>Dimethyl sulfide dynamics in first-year sea <span class="hlt">ice</span> melt ponds in the Canadian Arctic Archipelago</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Gourdal, Margaux; Lizotte, Martine; Massé, Guillaume; Gosselin, Michel; Poulin, Michel; Scarratt, Michael; Charette, Joannie; Levasseur, Maurice</p> <p>2018-05-01</p> <p>Melt pond formation is a seasonal pan-Arctic process. During the thawing season, melt ponds may cover up to 90 % of the Arctic first-year sea <span class="hlt">ice</span> (FYI) and 15 to 25 % of the multi-year sea <span class="hlt">ice</span> (MYI). These pools of water lying at the surface of the sea <span class="hlt">ice</span> cover are habitats for microorganisms and represent a potential source of the biogenic gas dimethyl sulfide (DMS) for the atmosphere. Here we report on the concentrations and dynamics of DMS in nine melt ponds sampled in July 2014 in the Canadian Arctic Archipelago. DMS concentrations were under the detection limit ( < 0.01 nmol L-1) in freshwater melt ponds and increased linearly with salinity (rs = 0.84, p ≤ 0.05) from ˜ 3 up to ˜ 6 nmol L-1 (avg. 3.7 ± 1.6 nmol L-1) in brackish melt ponds. This relationship suggests that the intrusion of <span class="hlt">seawater</span> in melt ponds is a key physical mechanism responsible for the presence of DMS. Experiments were conducted with water from three melt ponds incubated for 24 h with and without the addition of two stable isotope-labelled precursors of DMS (dimethylsulfoniopropionate), (D6-DMSP) and dimethylsulfoxide (13C-DMSO). Results show that de novo biological production of DMS can take place within brackish melt ponds through bacterial DMSP uptake and cleavage. Our data suggest that FYI melt ponds could represent a reservoir of DMS available for potential flux to the atmosphere. The importance of this <span class="hlt">ice</span>-related source of DMS for the Arctic atmosphere is expected to increase as a response to the thinning of sea <span class="hlt">ice</span> and the areal and temporal expansion of melt ponds on Arctic FYI.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C21B1120W','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C21B1120W"><span>Autonomous <span class="hlt">Ice</span> Mass Balance Buoys for Seasonal Sea <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Whitlock, J. D.; Planck, C.; Perovich, D. K.; Parno, J. T.; Elder, B. C.; Richter-Menge, J.; Polashenski, C. M.</p> <p>2017-12-01</p> <p>The <span class="hlt">ice</span> mass-balance represents the integration of all surface and ocean heat fluxes and attributing the impact of these forcing fluxes on the <span class="hlt">ice</span> cover can be accomplished by increasing temporal and spatial measurements. Mass balance information can be used to understand the ongoing changes in the Arctic sea <span class="hlt">ice</span> cover and to improve predictions of future <span class="hlt">ice</span> conditions. Thinner seasonal <span class="hlt">ice</span> in the Arctic necessitates the deployment of Autonomous <span class="hlt">Ice</span> Mass Balance buoys (IMB's) capable of long-term, in situ data collection in both <span class="hlt">ice</span> and open ocean. Seasonal IMB's (SIMB's) are free floating IMB's that allow data collection in thick <span class="hlt">ice</span>, thin <span class="hlt">ice</span>, during times of transition, and even open water. The newest generation of SIMB aims to increase the number of reliable IMB's in the Arctic by leveraging inexpensive commercial-grade instrumentation when combined with specially developed monitoring hardware. Monitoring tasks are handled by a custom, expandable data logger that provides low-cost flexibility for integrating a large range of instrumentation. The SIMB features ultrasonic sensors for direct measurement of both snow depth and <span class="hlt">ice</span> thickness and a digital temperature chain (DTC) for temperature measurements every 2cm through both snow and <span class="hlt">ice</span>. Air temperature and pressure, along with GPS data complete the Arctic picture. Additionally, the new SIMB is more compact to maximize deployment opportunities from multiple types of platforms.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/22652414','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/22652414"><span>A multi-beach study of Staphylococcus aureus, MRSA, and enterococci in <span class="hlt">seawater</span> and beach sand.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Goodwin, Kelly D; McNay, Melody; Cao, Yiping; Ebentier, Darcy; Madison, Melissa; Griffith, John F</p> <p>2012-09-01</p> <p>Incidences of Staphylococcus aureus and methicillin resistant S. aureus (MRSA) have risen worldwide prompting a need to better understand routes of human exposure and whether standard bacterial water quality monitoring practices adequately account for this potential threat. Beach water and sand samples were analyzed during summer months for S. aureus, enterococci, and MRSA at three southern California beaches (Avalon, Doheny, Malibu Surfrider). S. aureus frequently was detected in samples of <span class="hlt">seawater</span> (59%, n = 328) and beach sand (53%, n = 358). MRSA sometimes was detected in <span class="hlt">seawater</span> (1.6%, n = 366) and sand (2.7%, n = 366) at relatively low concentrations. Site specific differences were observed, with Avalon Beach presenting the highest concentrations of S. aureus and Malibu Surfrider the lowest in both <span class="hlt">seawater</span> and sand. S. aureus concentrations in <span class="hlt">seawater</span> and sand were correlated to each other and to a variety of other parameters. Multiple linear regression on the combined beach data indicated that significant explanatory variables for S. aureus in <span class="hlt">seawater</span> were S. aureus in sand, water temperature, enterococci in <span class="hlt">seawater</span>, and the number of swimmers. In sand, S. aureus concentrations were related to S. aureus in <span class="hlt">seawater</span>, water temperature, enterococci in <span class="hlt">seawater</span>, and inversely to surf height classification. Only the correlation to water temperature held for individually analyzed beaches and for S. aureus concentrations in both <span class="hlt">seawater</span> and sand. To provide context for these results, the prevalence of S. aureus in sand was compared to published fomite studies, and results suggested that beach prevalence was similar to that in homes. Published by Elsevier Ltd.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26911464','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26911464"><span>Cardiorespiratory upregulation during <span class="hlt">seawater</span> acclimation in rainbow trout: effects on gastrointestinal perfusion and postprandial responses.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Brijs, Jeroen; Gräns, Albin; Ekström, Andreas; Olsson, Catharina; Axelsson, Michael; Sandblom, Erik</p> <p>2016-05-01</p> <p>Increased gastrointestinal blood flow is essential for euryhaline fishes to maintain osmotic homeostasis during the initial phase of a transition from freshwater to <span class="hlt">seawater</span>. However, the cardiorespiratory responses and hemodynamic changes required for a successful long-term transition to <span class="hlt">seawater</span> remain largely unknown. In the present study, we simultaneously measured oxygen consumption rate (ṀO2), cardiac output (CO), heart rate (HR), and gastrointestinal blood flow (GBF) in rainbow trout (Oncorhynchus mykiss) acclimated to either freshwater or <span class="hlt">seawater</span> for at least 6 wk. <span class="hlt">Seawater</span>-acclimated trout displayed significantly elevated ṀO2 (day: 18%, night: 19%), CO (day: 22%, night: 48%), and GBF (day: 96%, night: 147%), demonstrating that an overall cardiorespiratory upregulation occurs during <span class="hlt">seawater</span> acclimation. The elevated GBF was achieved via a combination of increased CO, mediated through elevated stroke volume (SV), and a redistribution of blood flow to the gastrointestinal tract. Interestingly, virtually all of the increase in CO of <span class="hlt">seawater</span>-acclimated trout was directed to the gastrointestinal tract. Although unfed <span class="hlt">seawater</span>-acclimated trout displayed substantially elevated cardiorespiratory activity, the ingestion of a meal resulted in a similar specific dynamic action (SDA) and postprandial GBF response as in freshwater-acclimated fish. This indicates that the capacity for the transportation of absorbed nutrients, gastrointestinal tissue oxygen delivery, and acid-base regulation is maintained during digestion in <span class="hlt">seawater</span>. The novel findings presented in this study clearly demonstrate that euryhaline fish upregulate cardiovascular function when in <span class="hlt">seawater</span>, while retaining sufficient capacity for the metabolic and cardiovascular changes associated with the postprandial response. Copyright © 2016 the American Physiological Society.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013fss..book..383B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013fss..book..383B"><span>Spin <span class="hlt">Ice</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bramwell, Steven T.; Gingras, Michel J. P.; Holdsworth, Peter C. W.</p> <p>2013-03-01</p> <p>Pauling's model of hydrogen disorder in water <span class="hlt">ice</span> represents the prototype of a frustrated system. Over the years it has spawned several analogous models, including Anderson's model antiferromagnet and the statistical "vertex" models. Spin <span class="hlt">Ice</span> is a sixteen vertex model of "ferromagnetic frustration" that is approximated by real materials, most notably the rare earth pyrochlores Ho2Ti2O7, Dy2Ti2O7 and Ho2Sn2O7. These "spin <span class="hlt">ice</span> materials" have the Pauling zero point entropy and in all respects represent almost ideal realisations of Pauling's model. They provide experimentalists with unprecedented access to a wide variety of novel magnetic states and phase transitions that are located in different regions of the field-temperature phase diagram. They afford theoreticians the opportunity to explore many new features of the magnetic interactions and statistical mechanics of frustrated systems. This chapter is a comprehensive review of the physics -- both experimental and theoretical -- of spin <span class="hlt">ice</span>. It starts with a discussion of the historic problem of water <span class="hlt">ice</span> and its relation to spin <span class="hlt">ice</span> and other frustrated magnets. The properties of spin <span class="hlt">ice</span> are then discussed in three sections that deal with the zero field spin <span class="hlt">ice</span> state, the numerous field-induced states (including the recently identified "kagomé <span class="hlt">ice</span>") and the magnetic dynamics. Some materials related to spin <span class="hlt">ice</span> are briefly described and the chapter is concluded with a short summary of spin <span class="hlt">ice</span> physics.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25399173','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25399173"><span>Vapor deposition of water on graphitic surfaces: formation of amorphous <span class="hlt">ice</span>, bilayer <span class="hlt">ice</span>, <span class="hlt">ice</span> I, and liquid water.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Lupi, Laura; Kastelowitz, Noah; Molinero, Valeria</p> <p>2014-11-14</p> <p>Carbonaceous surfaces are a major source of atmospheric particles and could play an important role in the formation of <span class="hlt">ice</span>. Here we investigate through molecular simulations the stability, metastability, and molecular pathways of deposition of amorphous <span class="hlt">ice</span>, bilayer <span class="hlt">ice</span>, and <span class="hlt">ice</span> I from water vapor on graphitic and atomless Lennard-Jones surfaces as a function of temperature. We find that bilayer <span class="hlt">ice</span> is the most stable <span class="hlt">ice</span> polymorph for small cluster sizes, nevertheless it can grow metastable well above its region of thermodynamic stability. In agreement with experiments, the simulations predict that on increasing temperature the outcome of water deposition is amorphous <span class="hlt">ice</span>, bilayer <span class="hlt">ice</span>, <span class="hlt">ice</span> I, and liquid water. The deposition nucleation of bilayer <span class="hlt">ice</span> and <span class="hlt">ice</span> I is preceded by the formation of small liquid clusters, which have two wetting states: bilayer pancake-like (wetting) at small cluster size and droplet-like (non-wetting) at larger cluster size. The wetting state of liquid clusters determines which <span class="hlt">ice</span> polymorph is nucleated: bilayer <span class="hlt">ice</span> nucleates from wetting bilayer liquid clusters and <span class="hlt">ice</span> I from non-wetting liquid clusters. The maximum temperature for nucleation of bilayer <span class="hlt">ice</span> on flat surfaces, T(B)(max) is given by the maximum temperature for which liquid water clusters reach the equilibrium melting line of bilayer <span class="hlt">ice</span> as wetting bilayer clusters. Increasing water-surface attraction stabilizes the pancake-like wetting state of liquid clusters leading to larger T(B)(max) for the flat non-hydrogen bonding surfaces of this study. The findings of this study should be of relevance for the understanding of <span class="hlt">ice</span> formation by deposition mode on carbonaceous atmospheric particles, including soot.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/25894365','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/25894365"><span>Mining Critical Metals and Elements from <span class="hlt">Seawater</span>: Opportunities and Challenges.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Diallo, Mamadou S; Kotte, Madhusudhana Rao; Cho, Manki</p> <p>2015-08-18</p> <p>The availability and sustainable supply of technology metals and valuable elements is critical to the global economy. There is a growing realization that the development and deployment of the clean energy technologies and sustainable products and manufacturing industries of the 21st century will require large amounts of critical metals and valuable elements including rare-earth elements (REEs), platinum group metals (PGMs), lithium, copper, cobalt, silver, and gold. Advances in industrial ecology, water purification, and resource recovery have established that <span class="hlt">seawater</span> is an important and largely untapped source of technology metals and valuable elements. This feature article discusses the opportunities and challenges of mining critical metals and elements from <span class="hlt">seawater</span>. We highlight recent advances and provide an outlook of the future of metal mining and resource recovery from <span class="hlt">seawater</span>.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2012AGUFM.H51L..06S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2012AGUFM.H51L..06S"><span>A Simulation-Optimization Model for the Management of <span class="hlt">Seawater</span> Intrusion</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Stanko, Z.; Nishikawa, T.</p> <p>2012-12-01</p> <p><span class="hlt">Seawater</span> intrusion is a common problem in coastal aquifers where excessive groundwater pumping can lead to chloride contamination of a freshwater resource. Simulation-optimization techniques have been developed to determine optimal management strategies while mitigating <span class="hlt">seawater</span> intrusion. The simulation models are often density-independent groundwater-flow models that may assume a sharp interface and/or use equivalent freshwater heads. The optimization methods are often linear-programming (LP) based techniques that that require simplifications of the real-world system. However, <span class="hlt">seawater</span> intrusion is a highly nonlinear, density-dependent flow and transport problem, which requires the use of nonlinear-programming (NLP) or global-optimization (GO) techniques. NLP approaches are difficult because of the need for gradient information; therefore, we have chosen a GO technique for this study. Specifically, we have coupled a multi-objective genetic algorithm (GA) with a density-dependent groundwater-flow and transport model to simulate and identify strategies that optimally manage <span class="hlt">seawater</span> intrusion. GA is a heuristic approach, often chosen when seeking optimal solutions to highly complex and nonlinear problems where LP or NLP methods cannot be applied. The GA utilized in this study is the Epsilon-Nondominated Sorted Genetic Algorithm II (ɛ-NSGAII), which can approximate a pareto-optimal front between competing objectives. This algorithm has several key features: real and/or binary variable capabilities; an efficient sorting scheme; preservation and diversity of good solutions; dynamic population sizing; constraint handling; parallelizable implementation; and user controlled precision for each objective. The simulation model is <span class="hlt">SEAWAT</span>, the USGS model that couples MODFLOW with MT3DMS for variable-density flow and transport. ɛ-NSGAII and <span class="hlt">SEAWAT</span> were efficiently linked together through a C-Fortran interface. The simulation-optimization model was first tested by using a</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/18545964','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/18545964"><span>Different Planctomycetes diversity patterns in latitudinal surface <span class="hlt">seawater</span> of the open sea and in sediment.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Shu, Qinglong; Jiao, Nianzhi</p> <p>2008-04-01</p> <p>The 16S rRNA gene approach was applied to investigate the diversity of Planctomycetes in latitudinal surface <span class="hlt">seawater</span> of the Western Pacific Ocean. The results revealed that the Pirellula-Rhodopirellula-Blastopirellula clade dominated the Planctomycetes community at all surface <span class="hlt">seawater</span> sites while the minority genera Gemmata and Planctomyces were only found at sites H5 and H2 respectively. Although the clone frequency of the PRB clade seemed stable (between 83.3% and 94.1%) for all surface <span class="hlt">seawater</span> sites, the retrieved Pirellula-Rhodopirellula-Blastopirellula clade presented unexpected diversity. Interestingly, low latitude <span class="hlt">seawater</span> appeared to have higher diversity than mid-latitudes. integral-LIBSHUFF software analysis revealed significantly different diversity patterns between in latitudinal surface <span class="hlt">seawater</span> and in the sediment of South China Sea station M2896. Our data suggested that different hydrological and geographic features contributed to the shift of Planctomycetes diversity in marine environments. This is, to our knowledge, the first systematic assessment of Planctomycetes in latitudinal surface <span class="hlt">seawater</span> of the open sea and the first comparison of diversity pattern between surface <span class="hlt">seawater</span> and sediments and has broadened our understanding of Planctomycetes diversity in marine environments.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://www.dtic.mil/docs/citations/AD1013723','DTIC-ST'); return false;" href="http://www.dtic.mil/docs/citations/AD1013723"><span>Wave-<span class="hlt">Ice</span> interaction in the Marginal <span class="hlt">Ice</span> Zone: Toward a Wave-Ocean-<span class="hlt">Ice</span> Coupled Modeling System</span></a></p> <p><a target="_blank" href="http://www.dtic.mil/">DTIC Science & Technology</a></p> <p></p> <p>2015-09-30</p> <p>MIZ using WW3 (3 frequency bins, <span class="hlt">ice</span> retreat in August and <span class="hlt">ice</span> advance in October); Blue (solid): Based on observations near Antarctica by Meylan...1 DISTRIBUTION STATEMENT A. Approved for public release; distribution is unlimited. Wave- <span class="hlt">Ice</span> interaction in the Marginal <span class="hlt">Ice</span> Zone: Toward a...Wave-Ocean- <span class="hlt">Ice</span> Coupled Modeling System W. E. Rogers Naval Research Laboratory, Code 7322 Stennis Space Center, MS 39529 phone: (228) 688-4727</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2016EGUGA..18.1074H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2016EGUGA..18.1074H"><span>Mechanical sea-<span class="hlt">ice</span> strength parameterized as a function of <span class="hlt">ice</span> temperature</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Hata, Yukie; Tremblay, Bruno</p> <p>2016-04-01</p> <p>Mechanical sea-<span class="hlt">ice</span> strength is key for a better simulation of the timing of landlock <span class="hlt">ice</span> onset and break-up in the Canadian Arctic Archipelago (CAA). We estimate the mechanical strength of sea <span class="hlt">ice</span> in the CAA by analyzing the position record measured by the several buoys deployed in the CAA between 2008 and 2013, and wind data from the Canadian Meteorological Centre's Global Deterministic Prediction System (CMC_GDPS) REforecasts (CGRF). First, we calculate the total force acting on the <span class="hlt">ice</span> using the wind data. Next, we estimate upper (lower) bounds on the sea-<span class="hlt">ice</span> strength by identifying cases when the sea <span class="hlt">ice</span> deforms (does not deform) under the action of a given total force. Results from this analysis show that the <span class="hlt">ice</span> strength of landlock sea <span class="hlt">ice</span> in the CAA is approximately 40 kN/m on the landfast <span class="hlt">ice</span> onset (in <span class="hlt">ice</span> growth season). Additionally, it becomes approximately 10 kN/m on the landfast <span class="hlt">ice</span> break-up (in melting season). The <span class="hlt">ice</span> strength decreases with <span class="hlt">ice</span> temperature increase, which is in accord with results from Johnston [2006]. We also include this new parametrization of sea-<span class="hlt">ice</span> strength as a function of <span class="hlt">ice</span> temperature in a coupled slab ocean sea <span class="hlt">ice</span> model. The results from the model with and without the new parametrization are compared with the buoy data from the International Arctic Buoy Program (IABP).</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014AtmEn..88...14B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014AtmEn..88...14B"><span>Influence of spatial and temporal variability of subsurface soil moisture and temperature on <span class="hlt">vapour</span> intrusion</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Bekele, Dawit N.; Naidu, Ravi; Chadalavada, Sreenivasulu</p> <p>2014-05-01</p> <p>A comprehensive field study was conducted at a site contaminated with chlorinated solvents, mainly trichloroethylene (TCE), to investigate the influence of subsurface soil moisture and temperature on <span class="hlt">vapour</span> intrusion (VI) into built structures. Existing approaches to predict the risk of VI intrusion into buildings assume homogeneous or discrete layers in the vadose zone through which TCE migrates from an underlying source zone. In reality, the subsurface of the majority of contaminated sites will be subject to significant variations in moisture and temperature. Detailed site-specific data were measured contemporaneously to evaluate the impact of spatial and temporal variability of subsurface soil properties on VI exposure assessment. The results revealed that indoor air <span class="hlt">vapour</span> concentrations would be affected by spatial and temporal variability of subsurface soil moisture and temperature. The monthly monitoring of soil-gas concentrations over a period of one year at a depth of 3 m across the study site demonstrated significant variation in TCE <span class="hlt">vapour</span> concentrations, which ranged from 480 to 629,308 μg/m3. Soil-gas wells at 1 m depth exhibited high seasonal variability in TCE <span class="hlt">vapour</span> concentrations with a coefficient of variation 1.02 in comparison with values of 0.88 and 0.74 in 2 m and 3 m wells, respectively. Contour plots of the soil-gas TCE plume during wet and dry seasons showed that the plume moved across the site, hence locations of soil-gas monitoring wells for human risk assessment is a site specific decision. Subsurface soil-gas <span class="hlt">vapour</span> plume characterisation at the study site demonstrates that assessment for VI is greatly influenced by subsurface soil properties such as temperature and moisture that fluctuate with the seasons of the year.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5734655','PMC'); return false;" href="https://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=5734655"><span>UTLS water <span class="hlt">vapour</span> from SCIAMACHY limb measurementsV3.01 (2002–2012)</span></a></p> <p><a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pmc">PubMed Central</a></p> <p>Weigel, K.; Rozanov, A.; Azam, F.; Bramstedt, K.; Damadeo, R.; Eichmann, K.-U.; Gebhardt, C.; Hurst, D.; Kraemer, M.; Lossow, S.; Read, W.; Spelten, N.; Stiller, G. P.; Walker, K. A.; Weber, M.; Bovensmann, H.; Burrows, J. P.</p> <p>2017-01-01</p> <p>The SCanning Imaging Absorption spectroMeter for Atmospheric CHartographY (SCIAMACHY) aboard the Envisat satellite provided measurements from August 2002 until April 2012. SCIAMACHY measured the scattered or direct sunlight using different observation geometries. The limb viewing geometry allows the retrieval of water <span class="hlt">vapour</span> at about 10–25 km height from the near-infrared spectral range (1353–1410 nm). These data cover the upper troposphere and lower stratosphere (UTLS), a region in the atmosphere which is of special interest for a variety of dynamical and chemical processes as well as for the radiative forcing. Here, the latest data version of water <span class="hlt">vapour</span> (V3.01) from SCIAMACHY limb measurements is presented and validated by comparisons with data sets from other satellite and in situ measurements. Considering retrieval tests and the results of these comparisons, the V3.01 data are reliable from about 11 to 23 km and the best results are found in the middle of the profiles between about 14 and 20 km. Above 20 km in the extra tropics V3.01 is drier than all other data sets. Additionally, for altitudes above about 19 km, the vertical resolution of the retrieved profile is not sufficient to resolve signals with a short vertical structure like the tape recorder. Below 14 km, SCIAMACHY water <span class="hlt">vapour</span> V3.01 is wetter than most collocated data sets, but the high variability of water <span class="hlt">vapour</span> in the troposphere complicates the comparison. For 14–20 km height, the expected errors from the retrieval and simulations and the mean differences to collocated data sets are usually smaller than 10 % when the resolution of the SCIAMACHY data is taken into account. In general, the temporal changes agree well with collocated data sets except for the Northern Hemisphere extratropical stratosphere, where larger differences are observed. This indicates a possible drift in V3.01 most probably caused by the incomplete treatment of volcanic aerosols in the retrieval. In all other regions</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017DyAtO..79...10S','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017DyAtO..79...10S"><span>Sensitivity of open-water <span class="hlt">ice</span> growth and <span class="hlt">ice</span> concentration evolution in a coupled atmosphere-ocean-sea <span class="hlt">ice</span> model</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Shi, Xiaoxu; Lohmann, Gerrit</p> <p>2017-09-01</p> <p>A coupled atmosphere-ocean-sea <span class="hlt">ice</span> model is applied to investigate to what degree the area-thickness distribution of new <span class="hlt">ice</span> formed in open water affects the <span class="hlt">ice</span> and ocean properties. Two sensitivity experiments are performed which modify the horizontal-to-vertical aspect ratio of open-water <span class="hlt">ice</span> growth. The resulting changes in the Arctic sea-<span class="hlt">ice</span> concentration strongly affect the surface albedo, the ocean heat release to the atmosphere, and the sea-<span class="hlt">ice</span> production. The changes are further amplified through a positive feedback mechanism among the Arctic sea <span class="hlt">ice</span>, the Atlantic Meridional Overturning Circulation (AMOC), and the surface air temperature in the Arctic, as the Fram Strait sea <span class="hlt">ice</span> import influences the freshwater budget in the North Atlantic Ocean. Anomalies in sea-<span class="hlt">ice</span> transport lead to changes in sea surface properties of the North Atlantic and the strength of AMOC. For the Southern Ocean, the most pronounced change is a warming along the Antarctic Circumpolar Current (ACC), owing to the interhemispheric bipolar seasaw linked to AMOC weakening. Another insight of this study lies on the improvement of our climate model. The ocean component FESOM is a newly developed ocean-sea <span class="hlt">ice</span> model with an unstructured mesh and multi-resolution. We find that the subpolar sea-<span class="hlt">ice</span> boundary in the Northern Hemisphere can be improved by tuning the process of open-water <span class="hlt">ice</span> growth, which strongly influences the sea <span class="hlt">ice</span> concentration in the marginal <span class="hlt">ice</span> zone, the North Atlantic circulation, salinity and Arctic sea <span class="hlt">ice</span> volume. Since the distribution of new <span class="hlt">ice</span> on open water relies on many uncertain parameters and the knowledge of the detailed processes is currently too crude, it is a challenge to implement the processes realistically into models. Based on our sensitivity experiments, we conclude a pronounced uncertainty related to open-water sea <span class="hlt">ice</span> growth which could significantly affect the climate system sensitivity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2000mpse.conf...90K','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2000mpse.conf...90K"><span>Stability of Water <span class="hlt">Ice</span> Beneath Porous Dust Layers of the Martian South Polar Terrain</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Keller, H. U.; Skorov, Yu. V.; Markiewicz, W. J.; Basilevsky, A. T.</p> <p>2000-08-01</p> <p>The analysis of the Viking Infrared Thermal Mapper (IRTM) data show that the surface layers of the Mars south polar layered deposits have very low thermal inertia between 75 and 125 J/(sq m)(s-1/2)(K-1). This is consistent with the assumption that the surface is covered by a porous layer of fine dust. Paige and Keegan determined a slightly higher value based on a thermal model similar to that of Kieffer et al. In this model the heat transfer equation is used to estimate the thickness of the layer that protects the ground <span class="hlt">ice</span> from seasonal and diurnal temperature variations. The physical properties of the layer are unimportant as long as it has a low thermal inertia and conductivity and keeps the temperature at the <span class="hlt">ice</span> boundary low enough to prevent sublimation. A thickness between 20 and 4 cm was estimated. This result can be considered to be an upper limit. We assume the surface to be covered by a porous dust layer and consider the gas diffusion through it, from the ground <span class="hlt">ice</span> and from the atmosphere. Then the depth of the layer is determined by the mass flux balance of subliming and condensing water and not by the temperature condition. The dust particles in the atmosphere are of the order 1 gm. On the surface we can expect larger grains (up to sand size). Therefore assuming an average pore size of 10 gm, a volume porosity of 0.5, a heat capacity of 1300 J/(kg-1)(K-1) leads to a thermal inertia of approx. 80 J/(sq m)(s-1/2)(K-1). With these parameters a dust layer of only 5 mm thickness is found to establish the flux balance at the <span class="hlt">ice</span>-dust interface during spring season in the southern hemisphere at high latitudes (where Mars Polar Lander arrived). The diurnal temperature variation at the <span class="hlt">ice</span>-dust surface is shown. The maximum of 205 K well exceeds the sublimation temperature of water <span class="hlt">ice</span> at 198 K under the atmospheric conditions. The corresponding <span class="hlt">vapour</span> flux during the last day is shown together with the flux condensing from the atmosphere. The calculations</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2014PhDT.......122B','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2014PhDT.......122B"><span>Greenland <span class="hlt">ice</span> sheet retreat since the Little <span class="hlt">Ice</span> Age</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Beitch, Marci J.</p> <p></p> <p>Late 20th century and 21st century satellite imagery of the perimeter of the Greenland <span class="hlt">Ice</span> Sheet (GrIS) provide high resolution observations of the <span class="hlt">ice</span> sheet margins. Examining changes in <span class="hlt">ice</span> margin positions over time yield measurements of GrIS area change and rates of margin retreat. However, longer records of <span class="hlt">ice</span> sheet margin change are needed to establish more accurate predictions of the <span class="hlt">ice</span> sheet's future response to global conditions. In this study, the trimzone, the area of deglaciated terrain along the <span class="hlt">ice</span> sheet edge that lacks mature vegetation cover, is used as a marker of the maximum extent of the <span class="hlt">ice</span> from its most recent major advance during the Little <span class="hlt">Ice</span> Age. We compile recently acquired Landsat ETM+ scenes covering the perimeter of the GrIS on which we map area loss on land-, lake-, and marine-terminating margins. We measure an area loss of 13,327 +/- 830 km2, which corresponds to 0.8% shrinkage of the <span class="hlt">ice</span> sheet. This equates to an averaged horizontal retreat of 363 +/- 69 m across the entire GrIS margin. Mapping the areas exposed since the Little <span class="hlt">Ice</span> Age maximum, circa 1900 C.E., yields a century-scale rate of change. On average the <span class="hlt">ice</span> sheet lost an area of 120 +/- 16 km 2/yr, or retreated at a rate of 3.3 +/- 0.7 m/yr since the LIA maximum.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li class="active"><span>24</span></li> <li><a href="#" onclick='return showDiv("page_25");'>25</a></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_24 --> <div id="page_25" class="hiddenDiv"> <div class="row"> <div class="col-sm-12"> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div> </div> <div class="row"> <div class="col-sm-12"> <ol class="result-class" start="481"> <li> <p><a target="_blank" onclick="trackOutboundLink('https://images.nasa.gov/#/details-PIA11991.html','SCIGOVIMAGE-NASA'); return false;" href="https://images.nasa.gov/#/details-PIA11991.html"><span>Wilkins <span class="hlt">Ice</span> Shelf</span></a></p> <p><a target="_blank" href="https://images.nasa.gov/">NASA Image and Video Library</a></p> <p></p> <p>2009-04-20</p> <p>The Wilkins <span class="hlt">Ice</span> Shelf, as seen by NASA Terra spacecraft, on the western side of the Antarctic Peninsula, experienced multiple disintegration events in 2008. By the beginning of 2009, a narrow <span class="hlt">ice</span> bridge was all that remained to connect the <span class="hlt">ice</span> shelf to <span class="hlt">ice</span> fragments fringing nearby Charcot Island. That bridge gave way in early April 2009. Days after the <span class="hlt">ice</span> bridge rupture, on April 12, 2009, the Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) on NASA's Terra satellite acquired this image of the southern base of the <span class="hlt">ice</span> bridge, where it connected with the remnant <span class="hlt">ice</span> shelf. Although the <span class="hlt">ice</span> bridge has played a role in stabilizing the <span class="hlt">ice</span> fragments in the region, its rupture doesn't guarantee the <span class="hlt">ice</span> will immediately move away. http://photojournal.jpl.nasa.gov/catalog/PIA11991</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2013QSRv...79..168A','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2013QSRv...79..168A"><span>A review of sea <span class="hlt">ice</span> proxy information from polar <span class="hlt">ice</span> cores</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Abram, Nerilie J.; Wolff, Eric W.; Curran, Mark A. J.</p> <p>2013-11-01</p> <p>Sea <span class="hlt">ice</span> plays an important role in Earth's climate system. The lack of direct indications of past sea <span class="hlt">ice</span> coverage, however, means that there is limited knowledge of the sensitivity and rate at which sea <span class="hlt">ice</span> dynamics are involved in amplifying climate changes. As such, there is a need to develop new proxy records for reconstructing past sea <span class="hlt">ice</span> conditions. Here we review the advances that have been made in using chemical tracers preserved in <span class="hlt">ice</span> cores to determine past changes in sea <span class="hlt">ice</span> cover around Antarctica. <span class="hlt">Ice</span> core records of sea salt concentration show promise for revealing patterns of sea <span class="hlt">ice</span> extent particularly over glacial-interglacial time scales. In the coldest climates, however, the sea salt signal appears to lose sensitivity and further work is required to determine how this proxy can be developed into a quantitative sea <span class="hlt">ice</span> indicator. Methane sulphonic acid (MSA) in near-coastal <span class="hlt">ice</span> cores has been used to reconstruct quantified changes and interannual variability in sea <span class="hlt">ice</span> extent over shorter time scales spanning the last ˜160 years, and has potential to be extended to produce records of Antarctic sea <span class="hlt">ice</span> changes throughout the Holocene. However the MSA <span class="hlt">ice</span> core proxy also requires careful site assessment and interpretation alongside other palaeoclimate indicators to ensure reconstructions are not biased by non-sea <span class="hlt">ice</span> factors, and we summarise some recommended strategies for the further development of sea <span class="hlt">ice</span> histories from <span class="hlt">ice</span> core MSA. For both proxies the limited information about the production and transfer of chemical markers from the sea <span class="hlt">ice</span> zone to the Antarctic <span class="hlt">ice</span> sheets remains an issue that requires further multidisciplinary study. Despite some exploratory and statistical work, the application of either proxy as an indicator of sea <span class="hlt">ice</span> change in the Arctic also remains largely unknown. As information about these new <span class="hlt">ice</span> core proxies builds, so too does the potential to develop a more comprehensive understanding of past changes in sea</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2004SPIE.5544..356H','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2004SPIE.5544..356H"><span>Analytical approximations to <span class="hlt">seawater</span> optical phase functions of scattering</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Haltrin, Vladimir I.</p> <p>2004-11-01</p> <p>This paper proposes a number of analytical approximations to the classic and recently measured <span class="hlt">seawater</span> light scattering phase functions. The three types of analytical phase functions are derived: individual representations for 15 Petzold, 41 Mankovsky, and 91 Gulf of Mexico phase functions; collective fits to Petzold phase functions; and analytical representations that take into account dependencies between inherent optical properties of <span class="hlt">seawater</span>. The proposed phase functions may be used for problems of radiative transfer, remote sensing, visibility and image propagation in natural waters of various turbidity.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2008JApSc...8.1169M','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2008JApSc...8.1169M"><span>Low-Sulfate <span class="hlt">Seawater</span> Injection into Oil Reservoir to Avoid Scaling Problem</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Merdhah, Amer Badr Bin; Mohd Yassin, Abu Azam</p> <p></p> <p>This study presents the results of laboratory experiments carried out to investigate the formation of calcium, strontium and barium sulfates from mixing Angsi <span class="hlt">seawater</span> or low sulfate <span class="hlt">seawater</span> with the following sulfate contents (75, 50, 25, 5 and 1%) and formation water contain high concentration of calcium, strontium and barium ions at various temperatures (40-90°C) and atmospheric pressure. The knowledge of solubility of common oil field scale formation and how their solubilities are affected by changes in salinity and temperatures is also studied. Results show a large of precipitation occurred in all jars containing <span class="hlt">seawater</span> while the amount of precipitation decreased when the low sulfate <span class="hlt">seawater</span> was used. At higher temperatures the mass of precipitation of CaSO4 and SrSO4 scales increases and the mass of precipitation of BaSO4 scale decreases since the solubilities of CaSO4 and SrSO4 scales decreases and the solubility of BaSO4 increases with increasing temperature. It can be concluded that even at sulfate content of 1% there may still be a scaling problem.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/1999JQS....14..437T','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/1999JQS....14..437T"><span>Estimating past leaf-to-air <span class="hlt">vapour</span> pressure deficit from terrestrial plant 13C</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Turney, Chris S. M.; Barringer, James; Hunt, John E.; McGlone, Matt S.</p> <p>1999-08-01</p> <p>13C was determined in lignin extracted from present-day cladodes of Phyllocladus alpinus (a small coniferous tree) from seven well-lit sites across New Zealand. The 13C values ranged from -30.9 to -23.6 and were compared with monthly means of temperature, precipitation, relative humidity and <span class="hlt">vapour</span> pressure deficit from the nearest recording stations. Of these parameters, the leaf-to-air <span class="hlt">vapour</span> pressure deficit of the first month of cladode growth and expansion proved to be the most significantly correlated with lignin 13C, over a range of 0.3 to 0.8 kPa, confirming the importance of atmospheric moisture content on stomatal conductance. The carbon isotopic signature of lignin from fossilised cladodes preserved under the Kawakawa Tephra (22.6 k 14C yr BP) on the North Island is identical to that of the whole tissue, suggesting that for this species at least, fossil material can be used to approximate the lignin 13C. The 13C of species- and organ-specific fossil terrestrial plant material therefore provides an excellent method to quantify past changes in leaf-to-air <span class="hlt">vapour</span> pressure deficit.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/pages/biblio/1234340-extracting-uranium-from-seawater-promising-af-series-adsorbents','SCIGOV-DOEP'); return false;" href="https://www.osti.gov/pages/biblio/1234340-extracting-uranium-from-seawater-promising-af-series-adsorbents"><span>Extracting uranium from <span class="hlt">seawater</span>: Promising AF series adsorbents</span></a></p> <p><a target="_blank" href="http://www.osti.gov/pages">DOE PAGES</a></p> <p>Das, Sadananda; Oyola, Y.; Mayes, Richard T.; ...</p> <p>2015-11-02</p> <p>Here, a new family of high surface area polyethylene fiber adsorbents (AF series) was recently developed at the Oak Ridge National Laboratory (ORNL). The AF series of were synthesized by radiation-induced graft polymerization of acrylonitrile and itaconic acid (at different monomer/co-monomer mol ratios) onto high surface area polyethylene fibers. The degree of grafting (%DOG) of AF series adsorbents was found to be 154 354%. The grafted nitrile groups were converted to amidoxime groups by treating with hydroxylamine. The amidoximated adsorbents were then conditioned with 0.44M KOH at 80 C followed by screening at ORNL with simulated <span class="hlt">seawater</span> spiked with 8more » ppm uranium. Uranium adsorption capacity in simulated <span class="hlt">seawater</span> screening ranged from 170-200 g-U/kg-ads irrespective of %DOG. A monomer/co-monomer mol ratio in the range of 7.57-10.14 seemed to be optimum for highest uranium loading capacity. Subsequently, the adsorbents were also tested with natural <span class="hlt">seawater</span> at Pacific Northwest National Laboratory (PNNL) using flow-through exposure uptake experiments to determine uranium loading capacity with varying KOH conditioning time at 80 C. The highest adsorption capacity of AF1 measured after 56 days of marine testing was demonstrated as 3.9 g-U/kg-adsorbent and 3.2 g-U/kg-adsorbent for 1hr and 3hrs of KOH conditioning at 80 C, respectively. Based on capacity values of several AF1 samples, it was observed that changing KOH conditioning from 3hrs to 1hr at 80 C resulted in 22-27% increase in uranium loading capacity in <span class="hlt">seawater</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/1234340','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/1234340"><span>Extracting uranium from <span class="hlt">seawater</span>: Promising AF series adsorbents</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Das, Sadananda; Oyola, Y.; Mayes, Richard T.</p> <p></p> <p>Here, a new family of high surface area polyethylene fiber adsorbents (AF series) was recently developed at the Oak Ridge National Laboratory (ORNL). The AF series of were synthesized by radiation-induced graft polymerization of acrylonitrile and itaconic acid (at different monomer/co-monomer mol ratios) onto high surface area polyethylene fibers. The degree of grafting (%DOG) of AF series adsorbents was found to be 154 354%. The grafted nitrile groups were converted to amidoxime groups by treating with hydroxylamine. The amidoximated adsorbents were then conditioned with 0.44M KOH at 80 C followed by screening at ORNL with simulated <span class="hlt">seawater</span> spiked with 8more » ppm uranium. Uranium adsorption capacity in simulated <span class="hlt">seawater</span> screening ranged from 170-200 g-U/kg-ads irrespective of %DOG. A monomer/co-monomer mol ratio in the range of 7.57-10.14 seemed to be optimum for highest uranium loading capacity. Subsequently, the adsorbents were also tested with natural <span class="hlt">seawater</span> at Pacific Northwest National Laboratory (PNNL) using flow-through exposure uptake experiments to determine uranium loading capacity with varying KOH conditioning time at 80 C. The highest adsorption capacity of AF1 measured after 56 days of marine testing was demonstrated as 3.9 g-U/kg-adsorbent and 3.2 g-U/kg-adsorbent for 1hr and 3hrs of KOH conditioning at 80 C, respectively. Based on capacity values of several AF1 samples, it was observed that changing KOH conditioning from 3hrs to 1hr at 80 C resulted in 22-27% increase in uranium loading capacity in <span class="hlt">seawater</span>.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22311337-detecting-vapour-bubbles-simulations-metastable-water','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22311337-detecting-vapour-bubbles-simulations-metastable-water"><span>Detecting <span class="hlt">vapour</span> bubbles in simulations of metastable water</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>González, Miguel A.; Abascal, Jose L. F.; Valeriani, Chantal, E-mail: christoph.dellago@univie.ac.at, E-mail: cvaleriani@quim.ucm.es</p> <p>2014-11-14</p> <p>The investigation of cavitation in metastable liquids with molecular simulations requires an appropriate definition of the volume of the <span class="hlt">vapour</span> bubble forming within the metastable liquid phase. Commonly used approaches for bubble detection exhibit two significant flaws: first, when applied to water they often identify the voids within the hydrogen bond network as bubbles thus masking the signature of emerging bubbles and, second, they lack thermodynamic consistency. Here, we present two grid-based methods, the M-method and the V-method, to detect bubbles in metastable water specifically designed to address these shortcomings. The M-method incorporates information about neighbouring grid cells to distinguishmore » between liquid- and <span class="hlt">vapour</span>-like cells, which allows for a very sensitive detection of small bubbles and high spatial resolution of the detected bubbles. The V-method is calibrated such that its estimates for the bubble volume correspond to the average change in system volume and are thus thermodynamically consistent. Both methods are computationally inexpensive such that they can be used in molecular dynamics and Monte Carlo simulations of cavitation. We illustrate them by computing the free energy barrier and the size of the critical bubble for cavitation in water at negative pressure.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/20931628','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/20931628"><span><span class="hlt">Seawater</span> spray injury to Quercus acutissima leaves: crystal deposition, stomatal clogging, and chloroplast degeneration.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Kim, Ki Woo; Koo, Kyosang; Kim, Pan-Gi</p> <p>2011-05-01</p> <p>Effects of <span class="hlt">seawater</span> spray on leaf structure were investigated in Quercus acutissima by electron microscopy and X-ray microanalysis. Two-year-old seedlings of Q. acutissima were sprayed with <span class="hlt">seawater</span> and kept in a greenhouse maintained at 25°C. The most recognizable symptoms of <span class="hlt">seawater</span>-sprayed seedlings included leaf necrosis, crystal deposition, stomatal clogging, and chloroplast degeneration. Field emission scanning electron microscopy revealed that the leaf surface was covered with additional layers of remnants of <span class="hlt">seawater</span> spray. Composed of sodium and chloride, cube-shaped crystals (halite) were prevalently found on trichomes and epidermis, and formed aggregates. Meanwhile, wedge-shaped crystals were deposited on epidermis and consisted of calcium and sulfur. As a result of stomatal clogging by crystal deposition on the abaxial surface, it was conceivable that plant respiration became severely hampered. Transmission electron microscopy showed degenerated cytoplasm of <span class="hlt">seawater</span>-sprayed leaves. It was common to observe severe plasmolysis and disrupted chloroplasts with a reduced number of thylakoids in grana. These results indicate that foliar applications of <span class="hlt">seawater</span> were sufficient to induce necrosis of Q. acutissima seedlings as an abiotic disturbance factor. Copyright © 2010 Wiley-Liss, Inc.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/19021802','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/19021802"><span><span class="hlt">Ice</span> recrystallization inhibition in <span class="hlt">ice</span> cream by propylene glycol monostearate.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Aleong, J M; Frochot, S; Goff, H D</p> <p>2008-11-01</p> <p>The effectiveness of propylene glycol monostearate (PGMS) to inhibit <span class="hlt">ice</span> recrystallization was evaluated in <span class="hlt">ice</span> cream and frozen sucrose solutions. PGMS (0.3%) dramatically reduced <span class="hlt">ice</span> crystal sizes in <span class="hlt">ice</span> cream and in sucrose solutions frozen in a scraped-surface freezer before and after heat shock, but had no effect in quiescently frozen solutions. PGMS showed limited emulsifier properties by promoting smaller fat globule size distributions and enhanced partial coalescence in the mix and <span class="hlt">ice</span> cream, respectively, but at a much lower level compared to conventional <span class="hlt">ice</span> cream emulsifier. Low temperature scanning electron microscopy revealed highly irregular crystal morphology in both <span class="hlt">ice</span> cream and sucrose solutions frozen in a scraped-surface freezer. There was strong evidence to suggest that PGMS directly interacts with <span class="hlt">ice</span> crystals and interferes with normal surface propagation. Shear during freezing may be required for its distribution around the <span class="hlt">ice</span> and sufficient surface coverage.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/servlets/purl/6091444','SCIGOV-STC'); return false;" href="https://www.osti.gov/servlets/purl/6091444"><span>Arctic <span class="hlt">ice</span> islands</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Sackinger, W.M.; Jeffries, M.O.; Lu, M.C.</p> <p>1988-01-01</p> <p>The development of offshore oil and gas resources in the Arctic waters of Alaska requires offshore structures which successfully resist the lateral forces due to moving, drifting <span class="hlt">ice</span>. <span class="hlt">Ice</span> islands are floating, a tabular icebergs, up to 60 meters thick, of solid <span class="hlt">ice</span> throughout their thickness. The <span class="hlt">ice</span> islands are thus regarded as the strongest <span class="hlt">ice</span> features in the Arctic; fixed offshore structures which can directly withstand the impact of <span class="hlt">ice</span> islands are possible but in some locations may be so expensive as to make oilfield development uneconomic. The resolution of the <span class="hlt">ice</span> island problem requires two research steps: (1)more » calculation of the probability of interaction between an <span class="hlt">ice</span> island and an offshore structure in a given region; and (2) if the probability if sufficiently large, then the study of possible interactions between <span class="hlt">ice</span> island and structure, to discover mitigative measures to deal with the moving <span class="hlt">ice</span> island. The <span class="hlt">ice</span> island research conducted during the 1983-1988 interval, which is summarized in this report, was concerned with the first step. Monte Carlo simulations of <span class="hlt">ice</span> island generation and movement suggest that <span class="hlt">ice</span> island lifetimes range from 0 to 70 years, and that 85% of the lifetimes are less then 35 years. The simulation shows a mean value of 18 <span class="hlt">ice</span> islands present at any time in the Arctic Ocean, with a 90% probability of less than 30 <span class="hlt">ice</span> islands. At this time, approximately 34 <span class="hlt">ice</span> islands are known, from observations, to exist in the Arctic Ocean, not including the 10-meter thick class of <span class="hlt">ice</span> islands. Return interval plots from the simulation show that coastal zones of the Beaufort and Chukchi Seas, already leased for oil development, have <span class="hlt">ice</span> island recurrences of 10 to 100 years. This implies that the <span class="hlt">ice</span> island hazard must be considered thoroughly, and appropriate safety measures adopted, when offshore oil production plans are formulated for the Alaskan Arctic offshore. 132 refs., 161 figs., 17 tabs.« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://eric.ed.gov/?q=rate+AND+evaporation&id=EJ753861','ERIC'); return false;" href="https://eric.ed.gov/?q=rate+AND+evaporation&id=EJ753861"><span>Turkish Undergraduates' Misconceptions of Evaporation, Evaporation Rate, and <span class="hlt">Vapour</span> Pressure</span></a></p> <p><a target="_blank" href="http://www.eric.ed.gov/ERICWebPortal/search/extended.jsp?_pageLabel=advanced">ERIC Educational Resources Information Center</a></p> <p>Canpolat, Nurtac</p> <p>2006-01-01</p> <p>This study focused on students' misconceptions related to evaporation, evaporation rate, and <span class="hlt">vapour</span> pressure. Open-ended diagnostic questions were used with 107 undergraduates in the Primary Science Teacher Training Department in a state university in Turkey. In addition, 14 students from that sample were interviewed to clarify their written…</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017OSJ....52...43L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017OSJ....52...43L"><span>Fugacity analysis of polycyclic aromatic hydrocarbons between microplastics and <span class="hlt">seawater</span></span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Lee, Hwang; Chang, Sein; Kim, Seung-Kyu; Kwon, Jung-Hwan</p> <p>2017-03-01</p> <p>Recently, the accumulation of plastic debris in the marine environment has become a great concern worldwide. Although plastics are biologically and chemically inert, plastic debris has been suspected of causing adverse effects on ecosystems due to the increase in reactivity by size reduction and/or micropollutants associated with plastics. Because of the high sorption capacity of microplastics toward organic micropollutants, it is suspected that microplastics may play roles in the distribution and fate of micropollutants. In order to quantitatively evaluate the "net flow" of environmental contaminants in water-plastic-organism systems, a fugacity analysis was conducted using concentrations of polycyclic aromatic hydrocarbons (PAHs) in open oceans and in polyethylene as a representative material of plastic debris. Ratio of fugacity in polyethylene to that in <span class="hlt">seawater</span> showed a decreasing trend with increasing partition coefficient between polyethylene and <span class="hlt">seawater</span> (KPE/sw). This indicates that phase equilibrium between polyethylene and <span class="hlt">seawater</span> is not attained for higher molecular weight PAHs. Disequilibrium of high molecular weight PAHs suggests that transfer from <span class="hlt">seawater</span> to plastic debris is thermodynamically driven and the role of plastic debris as a vector to transfer them to living organisms would be minimal. However, additives may slowly migrate from plastics into the environment causing potentially serious effects on ecosystems.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://pubs.er.usgs.gov/publication/70074122','USGSPUBS'); return false;" href="https://pubs.er.usgs.gov/publication/70074122"><span>Physiological indices of <span class="hlt">seawater</span> readiness in postspawning steelhead kelts</span></a></p> <p><a target="_blank" href="http://pubs.er.usgs.gov/pubs/index.jsp?view=adv">USGS Publications Warehouse</a></p> <p>Buelow, Jessica; Moffitt, Christine M.</p> <p>2015-01-01</p> <p>Management goals to improve the recovery of steelhead (Oncorhynchus mykiss) stocks at risk of extinction include increasing the proportion of postspawning fish that survive and spawn again. To be successful, postspawning steelhead (kelts) migrating downstream to the ocean must prepare physiologically and physically for a <span class="hlt">seawater</span> transition. We sampled blood, gill filaments, and evaluated the external condition of migrating kelts from an ESA-listed population in the Snake/Columbia River system over two consecutive years to evaluate their physiological readiness for transition to <span class="hlt">seawater</span>. We chose attributes often considered as measures of preparation for <span class="hlt">seawater</span> in juveniles, including gill Na+,K+ ATPase activity, plasma electrolytes and hormones to consider factors related to external condition, size and sex. We found kelts in good external condition had plasma profiles similar to downstream-migrating smolts. In addition, we found more than 80% of kelts ranked in good external condition had smolt-like body silvering. We compared measures from migrating kelts with samples obtained from hatchery fish at the time of spawning to confirm that Na+, K+ ATPase activity in kelts was significantly elevated over spawning fish. We found significant differences in gill Na+, K+ ATPase activity in migrating kelts between the years of sampling, but little indication of influence of fish condition. We conclude that the postspawning steelhead sampled exhibited a suite of behaviours, condition and physiology characteristic of fish prepared for successful transition to a <span class="hlt">seawater</span> environment.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.osti.gov/biblio/22257828-uptake-uranium-from-seawater-amidoxime-based-polymeric-adsorbent-marine-testing','SCIGOV-STC'); return false;" href="https://www.osti.gov/biblio/22257828-uptake-uranium-from-seawater-amidoxime-based-polymeric-adsorbent-marine-testing"><span>Uptake of uranium from <span class="hlt">seawater</span> by amidoxime-based polymeric adsorbent marine testing</span></a></p> <p><a target="_blank" href="http://www.osti.gov/search">DOE Office of Scientific and Technical Information (OSTI.GOV)</a></p> <p>Tsouris, C.; Kim, J.; Oyola, Y.</p> <p>2013-07-01</p> <p>Amidoxime-based polymer adsorbents in the form of functionalized fibers were prepared at the Oak Ridge National Laboratory (ORNL) and screened in laboratory experiments, in terms of uranium uptake capacity, using spiked uranium solution and <span class="hlt">seawater</span> samples. Batch laboratory experiments conducted with 5-gallon <span class="hlt">seawater</span> tanks provided equilibrium information. Based on results from 5-gallon experiments, the best adsorbent was selected for field-testing of uranium adsorption from <span class="hlt">seawater</span>. Flow-through column tests have been performed at different marine sites to investigate the uranium uptake rate and equilibrium capacity under diverse biogeochemistry. The maximum amount of uranium uptake from <span class="hlt">seawater</span> tests at Sequim, WA, wasmore » 3.3 mg U/g adsorbent after eight weeks of contact of the adsorbent with <span class="hlt">seawater</span>. This amount was three times higher than the maximum adsorption capacity achieved in this study by a leading adsorbent developed by the Japan Atomic Energy Agency (JAEA), which was 1.1 mg U/g adsorbent at equilibrium. The initial uranium uptake rate of the ORNL adsorbent was 2.6 times higher than that of the JAEA adsorbent under similar conditions. A mathematical model derived from the mass balance of uranium was employed to describe the data. (authors)« less</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20010047828','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20010047828"><span><span class="hlt">Icing</span> Cloud Calibration of the NASA Glenn <span class="hlt">Icing</span> Research Tunnel</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Ide, Robert F.; Oldenburg, John R.</p> <p>2001-01-01</p> <p>The <span class="hlt">icing</span> research tunnel at the NASA Glenn Research Center underwent a major rehabilitation in 1999, necessitating recalibration of the <span class="hlt">icing</span> clouds. This report describes the methods used in the recalibration, including the procedure used to establish a uniform <span class="hlt">icing</span> cloud and the use of a standard <span class="hlt">icing</span> blade technique for measurement of liquid water content. The instruments and methods used to perform the droplet size calibration are also described. The liquid water content/droplet size operating envelopes of the <span class="hlt">icing</span> tunnel are shown for a range of airspeeds and compared to the FAA <span class="hlt">icing</span> certification criteria. The capabilities of the IRT to produce large droplet <span class="hlt">icing</span> clouds is also detailed.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('https://www.ncbi.nlm.nih.gov/pubmed/26787386','PUBMED'); return false;" href="https://www.ncbi.nlm.nih.gov/pubmed/26787386"><span>Interaction of <span class="hlt">ice</span> binding proteins with <span class="hlt">ice</span>, water and ions.</span></a></p> <p><a target="_blank" href="https://www.ncbi.nlm.nih.gov/entrez/query.fcgi?DB=pubmed">PubMed</a></p> <p>Oude Vrielink, Anneloes S; Aloi, Antonio; Olijve, Luuk L C; Voets, Ilja K</p> <p>2016-03-19</p> <p><span class="hlt">Ice</span> binding proteins (IBPs) are produced by various cold-adapted organisms to protect their body tissues against freeze damage. First discovered in Antarctic fish living in shallow waters, IBPs were later found in insects, microorganisms, and plants. Despite great structural diversity, all IBPs adhere to growing <span class="hlt">ice</span> crystals, which is essential for their extensive repertoire of biological functions. Some IBPs maintain liquid inclusions within <span class="hlt">ice</span> or inhibit recrystallization of <span class="hlt">ice</span>, while other types suppress freezing by blocking further <span class="hlt">ice</span> growth. In contrast, <span class="hlt">ice</span> nucleating proteins stimulate <span class="hlt">ice</span> nucleation just below 0 °C. Despite huge commercial interest and major scientific breakthroughs, the precise working mechanism of IBPs has not yet been unraveled. In this review, the authors outline the state-of-the-art in experimental and theoretical IBP research and discuss future scientific challenges. The interaction of IBPs with <span class="hlt">ice</span>, water and ions is examined, focusing in particular on <span class="hlt">ice</span> growth inhibition mechanisms.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20150002337','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20150002337"><span>Possible Mechanisms for Turbofan Engine <span class="hlt">Ice</span> Crystal <span class="hlt">Icing</span> at High Altitude</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Tsao, Jen-Ching; Struk, Peter M.; Oliver, Michael</p> <p>2014-01-01</p> <p>A thermodynamic model is presented to describe possible mechanisms of <span class="hlt">ice</span> formation on unheated surfaces inside a turbofan engine compression system from fully glaciated <span class="hlt">ice</span> crystal clouds often formed at high altitude near deep convective weather systems. It is shown from the analysis that generally there could be two distinct types of <span class="hlt">ice</span> formation: (1) when the "surface freezing fraction" is in the range of 0 to 1, dominated by the freezing of water melt from fully or partially melted <span class="hlt">ice</span> crystals, the <span class="hlt">ice</span> structure is formed from accretion with strong adhesion to the surface, and (2) when the "surface melting fraction" is the range of 0 to 1, dominated by the further melting of <span class="hlt">ice</span> crystals, the <span class="hlt">ice</span> structure is formed from accumulation of un-melted <span class="hlt">ice</span> crystals with relatively weak bonding to the surface. The model captures important qualitative trends of the fundamental <span class="hlt">ice</span>-crystal <span class="hlt">icing</span> phenomenon reported earlier1,2 from the research collaboration work by NASA and the National Research Council (NRC) of Canada. Further, preliminary analysis of test data from the 2013 full scale turbofan engine <span class="hlt">ice</span> crystal <span class="hlt">icing</span> test3 conducted in the NASA Glenn Propulsion Systems Laboratory (PSL) has also suggested that (1) both types of <span class="hlt">ice</span> formation occurred during the test, and (2) the model has captured some important qualitative trend of turning on (or off) the <span class="hlt">ice</span> crystal <span class="hlt">ice</span> formation process in the tested engine low pressure compressor (LPC) targeted area under different <span class="hlt">icing</span> conditions that ultimately would lead to (or suppress) an engine core roll back (RB) event.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://hdl.handle.net/2060/20160011109','NASA-TRS'); return false;" href="http://hdl.handle.net/2060/20160011109"><span>Possible Mechanisms for Turbofan Engine <span class="hlt">Ice</span> Crystal <span class="hlt">Icing</span> at High Altitude</span></a></p> <p><a target="_blank" href="http://ntrs.nasa.gov/search.jsp">NASA Technical Reports Server (NTRS)</a></p> <p>Tsao, Jen-Ching; Struk, Peter M.; Oliver, Michael J.</p> <p>2016-01-01</p> <p>A thermodynamic model is presented to describe possible mechanisms of <span class="hlt">ice</span> formation on unheated surfaces inside a turbofan engine compression system from fully glaciated <span class="hlt">ice</span> crystal clouds often formed at high altitude near deep convective weather systems. It is shown from the analysis that generally there could be two distinct types of <span class="hlt">ice</span> formation: (1) when the "surface freezing fraction" is in the range of 0 to 1, dominated by the freezing of water melt from fully or partially melted <span class="hlt">ice</span> crystals, the <span class="hlt">ice</span> structure is formed from accretion with strong adhesion to the surface, and (2) when the "surface melting fraction" is the range of 0 to 1, dominated by the further melting of <span class="hlt">ice</span> crystals, the <span class="hlt">ice</span> structure is formed from accumulation of un-melted <span class="hlt">ice</span> crystals with relatively weak bonding to the surface. The model captures important qualitative trends of the fundamental <span class="hlt">ice</span>-crystal <span class="hlt">icing</span> phenomenon reported earlier (Refs. 1 and 2) from the research collaboration work by NASA and the National Research Council (NRC) of Canada. Further, preliminary analysis of test data from the 2013 full scale turbofan engine <span class="hlt">ice</span> crystal <span class="hlt">icing</span> test (Ref. 3) conducted in the NASA Glenn Propulsion Systems Laboratory (PSL) has also suggested that (1) both types of <span class="hlt">ice</span> formation occurred during the test, and (2) the model has captured some important qualitative trend of turning on (or off) the <span class="hlt">ice</span> crystal <span class="hlt">ice</span> formation process in the tested engine low pressure compressor (LPC) targeted area under different <span class="hlt">icing</span> conditions that ultimately would lead to (or suppress) an engine core roll back (RB) event.</p> </li> <li> <p><a target="_blank" onclick="trackOutboundLink('http://adsabs.harvard.edu/abs/2017AGUFM.C51A0955L','NASAADS'); return false;" href="http://adsabs.harvard.edu/abs/2017AGUFM.C51A0955L"><span>Sea <span class="hlt">ice</span> roughness: the key for predicting Arctic summer <span class="hlt">ice</span> albedo</span></a></p> <p><a target="_blank" href="http://adsabs.harvard.edu/abstract_service.html">NASA Astrophysics Data System (ADS)</a></p> <p>Landy, J.; Ehn, J. K.; Tsamados, M.; Stroeve, J.; Barber, D. G.</p> <p>2017-12-01</p> <p>Although melt ponds on Arctic sea <span class="hlt">ice</span> evolve in stages, <span class="hlt">ice</span> with smoother surface topography typically allows the pond water to spread over a wider area, reducing the <span class="hlt">ice</span>-albedo and accelerating further melt. Building on this theory, we simulated the distribution of meltwater on a range of statistically-derived topographies to develop a quantitative relationship between premelt sea <span class="hlt">ice</span> surface roughness and summer <span class="hlt">ice</span> albedo. Our method, previously applied to ICESat observations of the end-of-winter sea <span class="hlt">ice</span> roughness, could account for 85% of the variance in AVHRR observations of the summer <span class="hlt">ice</span>-albedo [Landy et al., 2015]. Consequently, an Arctic-wide reduction in sea <span class="hlt">ice</span> roughness over the ICESat operational period (from 2003 to 2008) explained a drop in <span class="hlt">ice</span>-albedo that resulted in a 16% increase in solar heat input to the sea <span class="hlt">ice</span> cover. Here we will review this work and present new research linking pre-melt sea <span class="hlt">ice</span> surface roughness observations from Cryosat-2 to summer sea <span class="hlt">ice</span> albedo over the past six years, examining the potential of winter roughness as a significant new source of sea <span class="hlt">ice</span> predictability. We will further evaluate the possibility for high-resolution (kilometre-scale) forecasts of summer sea <span class="hlt">ice</span> albedo from waveform-level Cryosat-2 roughness data in the landfast sea <span class="hlt">ice</span> zone of the Canadian Arctic. Landy, J. C., J. K. Ehn, and D. G. Barber (2015), Albedo feedback enhanced by smoother Arctic sea <span class="hlt">ice</span>, Geophys. Res. Lett., 42, 10,714-10,720, doi:10.1002/2015GL066712.</p> </li> </ol> <div class="pull-right"> <ul class="pagination"> <li><a href="#" onclick='return showDiv("page_1");'>«</a></li> <li><a href="#" onclick='return showDiv("page_21");'>21</a></li> <li><a href="#" onclick='return showDiv("page_22");'>22</a></li> <li><a href="#" onclick='return showDiv("page_23");'>23</a></li> <li><a href="#" onclick='return showDiv("page_24");'>24</a></li> <li class="active"><span>25</span></li> <li><a href="#" onclick='return showDiv("page_25");'>»</a></li> </ul> </div> </div><!-- col-sm-12 --> </div><!-- row --> </div><!-- page_25 --> <div class="footer-extlink text-muted" style="margin-bottom:1rem; text-align:center;">Some links on this page may take you to non-federal websites. 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