1,979 research outputs found

    Oligocene Deep Water Export from the North Atlantic and the Development of the Antarctic Circumpolar Current Examined with Neodymium Isotopes

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    Neodymium (Nd) isotopes were measured on 181 samples of fossil fish teeth recovered from Oligocene toMiocene sections at Ocean Drilling Program Site 1090 (3700 m water depth) on Agulhas Ridge in the Atlanticsector of the Southern Ocean. A long-term decreasing trend toward less radiogenic Nd isotope compositionsdominates the record. This trend is interrupted by shifts toward more radiogenic compositions near the early/lateOligocene boundary and the Oligocene/Miocene boundary. Overall, eNd values at Agulhas Ridge are moreradiogenic than at other Atlantic locations, and are similar to those at Indian Ocean locations. The pattern ofvariability is remarkably similar to Nd isotope results from Walvis Ridge (South Atlantic) and Ninetyeast Ridge(Indian Ocean). In contrast, Agulhas Ridge and Maud Rise Nd isotope records do not show similar patterns overthis interval. Results from this study indicate that deep water in the Atlantic flowed predominantly from north tosouth during the Oligocene and Miocene, and that export of Northern Component Water (NCW) to the SouthernOcean increased in the late Oligocene. There is also evidence for efficient exchange of deep waters between theAtlantic sector of the Southern Ocean and the Indian Ocean, although the direction of deep water flow is notentirely clear from these data. The shifts to more radiogenic Nd isotopic compositions most likely representincreases in the flux of Pacific waters through Drake Passage, and the timing of these events reflect developmentof a mature Antarctic Circumpolar Current (ACC). The relative timing of increased NCW export and ACCmaturation support hypotheses that link deep water formation in the North Atlantic to the opening of DrakePassage

    Advanced Engineering Laboratory project summaries 1989

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    The Advanced Engineering Laboratory of the Woods Hole Oceanographic Institution is a development laboratory within the Applied Ocean Physics and Engineering Department. Its function is the development of oceanographic instrumentation to test developing theories in ocean physics, and to enhance current research projects in other disciplines within the oceanographic community. This report summarizes recent and ongoing projects performed by members of the laboratory

    OCEANIC FLUXES FROM PROGLACIAL AND DEGLACIAL WATERSHEDS IN WESTERN GREENLAND

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    Weathering in western Greenland occurs in two distinct environments: proglacial watersheds that extend from the margin of the Greenland Ice Sheet (GIS) and derive water from ice melt, and deglacial watersheds that develop on terrains unconnected to the GIS and derive water from annual precipitation. Proglacial and deglacial watersheds currently provide equal amounts of runoff in western Greenland. These watersheds may contribute different solute fluxes to the oceans depending on exposure age, climate, and weathering environment. We test this hypothesis by comparing chemical compositions of streams in four deglacial watersheds (Sisimiut, Nerumaq, Qorlortoq, Kangerlussuaq) and one proglacial watershed (Watson River Akuliarusiarsuup Kuua River; AKR) along a ~160 km transect from the coast to the GIS. Recent work found that weathering reactions in the deglacial watersheds shift from being dominated by carbonate dissolution inland to sulfide oxidation near the coast. Silicate weathering, based on increased Si, Na and K concentrations, is a minor source of solutes to deglacial streams and is less extensive near the GIS than the coast, where older moraines experience greater precipitation. In general, specific conductivity (SpC: 48-301 μS/cm) and pH (7.0-8.2) increase inland as precipitation decreases and fresh mineral surfaces become more common. The AKR, in contrast, has lower average SpC (11.9 uS/cm) and pH (6.86) than the deglacial streams. Low SpC reflects dilution by ice melt and short residence time of water in the subglacial system. Proglacial flow is enriched in Si compared to deglacial flow particularly near headwaters, indicating higher silicate weathering rates in the pro- and sub-glacial systems. Low pH values indicate: 1) equilibration with atmospheric CO2 in the supraglacial system near headwaters, and 2) acid production generated by sulfide oxidation in the hyporheic zone identified by elevated SO4 concentrations. However, Ca, Mg and HCO3 are the dominant ions over the length of the AKR indicating that dissolution of carbonate is the predominant form of weathering. Our results indicate the two types of watersheds provide distinct fluxes of solutes to the oceans that are likely to change as ice sheets retreat and advance with changing climate

    Hydrologic exchange and chemical weathering in a proglacial watershed near Kangerlussuaq, west Greenland

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    The exchange of proglacial river water with active layer pore water could alter water chemical compositions in glacial outwash plains and oceanic solute fluxes. To evaluate effects of this exchange, we sampled Watson River and adjacent pore water during the 2013 melt season at two sandurs in western Greenland; one in Sandflugtdalen and the other near the confluence with Søndre Strømfjord. We measured temperature, specific conductivity, and head gradients between the river and bank over a week-long period at Sandflugtdalen, as well as sediment hydraulic conductivity and chemical compositions of waters from both sites. Specific conductivity of pore water is four to ten times greater than river water as solutes are concentrated from weathering reactions, cryoconcentration, and evaporation. Pore water compositions are predominantly altered by carbonate dissolution and sulfide mineral oxidation. High concentrations of HCO3 and SO4 result from solute recycling and dissolution of secondary Ca-Mg carbonate/sulfate salts initially formed by near-surface evaporation in the summer and at depth by freeze-in of the active layer and cryoconcentration in the winter. High hydraulic conductivity (10−5 to 10−4 m/s) and diurnal fluctuations of river stage during our study caused exchange of river and pore water immediately adjacent to the river channel, with a net loss of river water to the bank. Pore water \u3e6 m from the river continuously flowed away from the river. Approximately 1–8% of the river discharge through the Sandflugtdalen was lost to the river bank during our 6.75 day study based on calculations using Darcy’s Law. Although not sampled, some of this water should discharge to the river during low river stage early and late in the melt season. Elevated pore water solute concentrations in sandurs and water exchange at diurnal and seasonal frequency should impact fluxes of solutes to the ocean, although understanding the magnitude of this effect will require long-term evaluation throughout the melt season

    The role of tissue transglutaminase in 1-methyl-4-phenylpyridinium (MPP+)-induced toxicity in differentiated human SH-SY5Y neuroblastoma cells

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    Tissue transglutaminase (TG2) can induce post-translational modification of proteins, resulting in protein cross-linking or incorporation of polyamines into substrates, and can also function as a signal transducing G protein. The role of TG2 in the formation of insoluble cross-links has led to its implication in some neurodegenerative conditions. Exposure of pre-differentiated SH-SY5Y cells to the Parkinsonian neurotoxin 1-methyl-4-phenylpyridinium ion (MPP+) resulted in significant dose-dependent reductions in TG2 protein levels, measured by probing Western blots with a TG2-specific antibody. Transglutaminase (TG) transamidating activity, on the other hand, monitored by incorporation of a polyamine pseudo-substrate into cellular proteins, was increased. Inhibitors of TG (putrescine) and TG2 (R283) exacerbated MPP+ toxicity, suggesting that activation of TG2 may promote a survival response in this toxicity paradigm

    The seawater neodymium and lead isotope record of the final stages of Central American Seaway closure

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    Key Points: Seawater Nd and Pb isotope records for the Pliocene Caribbean and EEP Caribbean Nd isotope composition became more UNADW-like during the Pliocene Short term changes support link between CAS closure and strength of AMOC The shoaling and final closure of the Central American Seaway (CAS) resulted in a major change of the global ocean circulation and has been suggested as an essential driver for strengthening of Atlantic Meridional Overturning Circulation (AMOC). The exact timing of CAS closure is key to interpreting its importance. Here we present a reconstruction of deep and intermediate water Nd and Pb isotope compositions obtained from fossil fish teeth and the authigenic coatings of planktonic foraminifera in the eastern equatorial Pacific (ODP Site 1241) and the Caribbean (ODP Sites 998, 999 and 1000) covering the final stages of CAS closure between 5.6 and 2.2 Ma. The data for the Pacific site indicate no significant Atlantic/Caribbean influence over this entire period. The Caribbean sites show a continuous trend to less radiogenic Nd isotope compositions during the Pliocene, consistent with an enhancement of Upper North Atlantic Deep Water (UNADW) inflow and a strengthening of the AMOC. Superimposed onto this long-term trend, shorter-term changes of intermediate Caribbean Nd isotope signatures approached more UNADW-like values during intervals when published reconstructions of seawater salinity suggested complete closure of the CAS. The data imply that significant deep water exchange with the Pacific essentially stopped by 7 Ma and that shallow exchange, which still occurred at least periodically until approximately 2.5 Ma, may have been linked to the strength of the AMOC but did not have any direct effect on the intermediate and deep Caribbean Nd isotope signatures through mixing with Pacific waters

    Heterogeneous CO\u3csub\u3e2\u3c/sub\u3eand CH\u3csub\u3e4\u3c/sub\u3eContent of Glacial Meltwater From the Greenland Ice Sheet and Implications for Subglacial Carbon Processes

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    Accelerated melting of the Greenland Ice Sheet has increased freshwater delivery to the Arctic Ocean and amplified the need to understand the impact of Greenland Ice Sheet meltwater on Arctic greenhouse gas budgets. We evaluate subglacial discharge from the Greenland Ice Sheet for carbon dioxide (CO2) and methane (CH4) concentrations and δ13C values and use geochemical models to evaluate subglacial CH4 and CO2 sources and sinks. We compare discharge from southwest (a sub-catchment of the Isunnguata Glacier, sub-Isunnguata, and the Russell Glacier) and southern Greenland (Kiattut Sermiat). Meltwater CH4 concentrations vary by orders of magnitude between sites and are saturated with respect to atmospheric concentrations at Kiattut Sermiat. In contrast, meltwaters from southwest sites are supersaturated, even though oxidation reduces CH4 concentrations by up to 50 % during periods of low discharge. CO2 concentrations range from supersaturated at sub-Isunnguata to undersaturated at Kiattut Sermiat. CO2 is consumed by mineral weathering throughout the melt season at all sites; however, differences in the magnitude of subglacial CO2 sources result in meltwaters that are either sources or sinks of atmospheric CO2. At the sub-Isunnguata site, the predominant source of CO2 is organic matter (OM) remineralization. However, multiple or heterogeneous subglacial CO2 sources maintain atmospheric CO2 concentrations at Russell but not at Kiattut Sermiat, where CO2 is undersaturated. These results highlight a previously unrecognized degree of heterogeneity in greenhouse gas dynamics under the Greenland Ice Sheet. Future work should constrain the extent and controls of heterogeneity to improve our understanding of the impact of Greenland Ice Sheet melt on Arctic greenhouse gas budgets, as well as the role of continental ice sheets in greenhouse gas variations over glacial–interglacial timescales

    SEASONAL EVOLUTION AND SPATIAL DISTRIBUTION OF WEATHERING IN WESTERN GREENLAND

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    Through physical weathering, the Greenland Ice Sheet (GIS) produces sediments which are subsequently chemically weathered in three types of watersheds: 1) deglacial watersheds that are physically disconnected from the GIS and drain local precipitation, 2) proglacial watersheds that are hydrologically connected to the GIS, and 3) subglacial watersheds that form beneath the GIS. Chemical weathering in the glacial foreland may be important to atmospheric CO2 drawdown and oceanic fluxes of solutes, yet no holistic study exists that compares solute sources across all types of watersheds and through the melt season. Consequently, we investigated spatiotemporal changes in weathering through the 2013 ablation season from a transect of watersheds spanning the coast to the GIS in western Greenland. We sampled one proglacial (PG) watershed, from which we also assess subglacial (SG) weathering, one inland deglacial (IDG) and one coastal deglacial (CDG) watershed. A simple stoichiometric mass balance quantifies solute sources in each watershed. The principal solute source is trace carbonates in all watersheds; however, IDG has more carbonate (61 vs 36 mol%) and less silicate (3 vs 14 mol%) weathering than CDG. PG has similar carbonate (41 mol%) and silicate weathering (16 mol%) proportions to CDG, despite proximity to IDG. Weathering of biotite decreases from 12 mol% at PG to 3 mol% at CDG along an exposure age gradient, consistent with more radiogenic 87Sr/86Sr in waters at PG (0.73556) than DGC (0.71114). Carbonate weathering decreases and biotite + silicate weathering increases downstream through PG, reflecting increased weathering. Solute sources change little through time or space at IDG, but at PG, silicate weathering increases and carbonate weathering decreases as flow increases through the melt season, consistent with increased contributions of SG waters with long residence times in distributed channels. Thus, the evolution of SG through time and connections between subglacial reservoirs and main flow paths plays an important role in weathering at PG. As the GIS retreats, deglacial watersheds will constitute a greater fraction of the weathering flux and thus increased silicate weathering should alter solute fluxes to the oceans and increase atmospheric CO2 drawdown

    A Helium-Surface Interaction Potential of Bi2_2Te3_3(111) from Ultrahigh-Resolution Spin-Echo Measurements

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    We have determined an atom-surface interaction potential for the He−-Bi2_2Te3_3(111) system by analysing ultrahigh resolution measurements of selective adsorption resonances. The experimental measurements were obtained using 3^3He spin-echo spectrometry. Following an initial free-particle model analysis, we use elastic close-coupling calculations to obtain a three-dimensional potential. The three-dimensional potential is then further refined based on the experimental data set, giving rise to an optimised potential which fully reproduces the experimental data. Based on this analysis, the He−-Bi2_2Te3_3(111) interaction potential can be described by a corrugated Morse potential with a well depth D=(6.22±0.05) meVD=(6.22\pm0.05)~\mathrm{meV}, a stiffness κ=(0.92±0.01) A˚−1\kappa =(0.92\pm0.01)~\mathrm{\AA}^{-1} and a surface electronic corrugation of (9.6±0.2)(9.6\pm0.2)% of the lattice constant. The improved uncertainties of the atom-surface interaction potential should also enable the use in inelastic close-coupled calculations in order to eventually study the temperature dependence and the line width of selective adsorption resonances
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