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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 276 (1978), S. 811-813 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Figure 1 shows that the sediment thickness is quite variable even over a small area of the valley floor. Core 4A (132 cm of sediment) and core 4G (15 cm of sediment) both terminated with basaltic glass, and a core from site 4C recovered glass only, with no overlying sediment. A study of bottom ...
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Digestive diseases and sciences 22 (1977), S. 189-194 
    ISSN: 1573-2568
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The effect of fasting on bile lithogenicity was studied in 19 normal men and 22 normal women. The molar percentages of bile acid, phospholipid, and cholesterol, determined after random overnight fasts of 9, 12, and 16 hr, were plotted on triangular coordinates. The molar percentage of cholesterol increased in both men and women. Analysis using Admirand and Small's criteria for cholesterol saturation revealed that 4.50% of normal women were lithogenic at 9.1 hr and 54.5% at 16.5 hr (P〈0.005). A similar trend in men was not significant. The mean values for both sexes were lithogenic at 16 hr only. Lithogenic bile was present in 4 men and 1 woman at 9 hr fasting and became more lithogenic with longer fasting. Analysis using the criteria of Hegardt and Dam revealed an increased proportion of both sexes moving into the metastable-labile and supersaturated zones on fasting, again with significant changes for women (P〈0.01). The duration of fasting is important in interpreting the presence of lithogenic bile; although more pronounced in women, both sexes showed increased cholesterol saturation in bile with fasting.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 5 (1999), S. 87-97 
    ISSN: 1573-1421
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Experimental evidence suggests that formation of metal sulfides in anoxic sediments limits the bioavailability of several toxic elements. Our ability to quantify the processes by which these metal sulfides form is dependent upon our ability to determine the speciation of solid phase metals in sediments. Our work indicates that an entire suite of Cu-Fe and Ni-Fe sulfide minerals can form upon the exposure of mackinawite to aqueous Cu and Ni. Furthermore, we have demonstrated that the solubility of pure metal sulfide minerals and their iron-metal derivatives in HCl directly correlates with the observed trends in the ''Degree of Trace Metal Pyritization'' in natural sediments. Current extraction schemes cannot distinguish discrete trace metal sulfides from trace metals associated with pyrite.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 1 (1995), S. v 
    ISSN: 1573-1421
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 4 (1998), S. 301-319 
    ISSN: 1573-1421
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Relatively soon (∼0.2 Ga) after the Earthformed, it is likely that major oceans appeared in ahot (∼100°C) reducing environment where carbondioxide was probably the dominant atmospheric gas,with PCO2, values reaching perhaps in excess of 10atm. During the Hadean Eon between 4.3 and 3.8 Ga BP,major changes in the concentration of atmosphericCO2 and associated temperature changes had aprofound influence on the carbonate geochemistry ofthe Hadean Ocean. Although no rocks are known to havesurvived prior to the Archean Eon, it is stillpossible to calculate approximate values for importantseawater parameters during the Hadean Eon based onother sources of information and reasonableassumptions about processes such as weatheringreactions. Our calculations are based on a linear temperaturechange from 100°C to 70°C and logPCO2 change from 1 to -1.5 over the Hadean Eon. Over this range in temperature and P CO2, theinfluence of T is relatively small, but changes inP CO2 result in large compositional variations inthe carbonate chemistry of Hadean seawater. In theearly Hadean, seawater pH was probably about5.8 ± ∼ 0.2, DIC may have reached close to 130 mM,and alkalinity was perhaps close to 30 mM. By thelate Hadean, seawater pH probably had changed to closeto neutral (∼6.8), and DIC and alkalinity were closerto present-day values. Even large uncertainties inNa+ + Cl-, K+ and Mg2+concentrations produce relatively small uncertaintiesin our calculated values for the carbonic acid system. However, larger uncertainties result from reasonableranges for Ca2+ concentrations and the saturationstate of Hadean seawater with respect to calcite. Our calculations support the hypothesis that acarbonate chemistry of seawater roughly similar tothat of modern oceans could have been acquired veryearly in Earth history. If seawater composition werebuffered by reactions involving carbonates andsilicates, then the composition of late Hadean-earlyArchean seawater was not vastly different from that oftoday. Thus, by the conclusion of the Hadean Eon, ifnot before, environmental conditions at the Earth's surface, including temperature and seawatercomposition, were sufficiently equable for theevolution of life, including the Archaebacteria: theextreme halophiles and thermophiles and methanogens.Contrary to the hypothesis of an early Na-bicarbonateocean, our calculations suggest the possibility thatthe early oceans of Earth were a NaCl-dominatedaqueous solution, with somewhat higher DIC andalkalinity concentrations, higher saturation state,and the possibility of lower calcium concentrations.The time course of approach of Hadean seawater to acarbonate composition closer to that of today isdifficult to predict. It is distinctly possible thatthe concentration of calcium in seawater did not reachlevels like that of modern seawater until the latePrecambrian and thus constrained the timing of the"Big Bang" of organic evolution, the emergence of theshelled invertebrates at the beginning of thePhanerozoic.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 5 (1999), S. 75-85 
    ISSN: 1573-1421
    Keywords: Sulfides ; pyrite ; anoxic sediments ; iron
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The formation of sedimentary iron sulfides was studied in sandy sediments of the Laguna Madre, TX, in order to better understand how this process operates in sediments where reactive iron is likely to be limiting for sulfide mineral formation. These sediments usually had reactive iron and total reduced sulfide concentrations one to two orders of magnitude less than in typical shallow water terrigenous muds, but organic-C concentrations typical of fine-grained sediments due to the extensive presence of seagrass beds. This resulted in moderate (0–150 μm) dissolved H2S concentrations with maximum concentrations in the upper (3–:5 cm) root zone. Based on citrate dithionite extractable-Fe the degree of sulfidization was usually 100% or greater. Acid volatile sulfides (AVS) typically comprised roughly 60% of total reduced sulfur and the proportion of AVS generally increased instead of decreasing with depth. The unusual proportion of TRS as AVS and persistence of AVS are attributed to exceptionally slow pyrite formation kinetics. The probable reasons for these slow reaction kinetics are the high (〉7.8) pH of the sediments, which favors the slow polysulfide pathway for pyrite formation, high (typically about 2–4 mm) dissolved organic carbon concentrations that inhibit growth of pyrite and the low concentration of reactants which greatly increases the average transport distances necessary for diffusion controlled reactions.
    Type of Medium: Electronic Resource
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