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Gas concentrations and isotopic compositions of water have been measured in hydrothermal waters from 13°N on the East Pacific Rise. In the most Mg-depleted samples ( 5 × 10−3 moles/kg) the gas concentrations are: 3–4.5 × 10−5 cm3 STP/kg helium, 0.62–1.24 cm3 STP/kg CH4, 10.80–16.71 × 10−3 moles/kg CO2. The samples contain large quantities (95–126 cm3/kg) of H2 and some carbon monoxide (0.26–0.36 cm3/kg) which result from reaction with the titanium sampling bottles. δ13C in methane and CO2 (−16.6 to −19.5 and −4.1 to −5.5 respectively) indicate temperatures between 475 and 550°C, whereas δ13CCO is compatible with formation by reduction of CO2 on Ti at 350°C close to the sampling temperature.3He/4He are very homogeneous at (7.5 ± 0.1)RA(3He/4He = 1.0 × 10−5) and very similar to already published data as well as CH4/3He ratios between 1.4 and 2.1 × 106.18O and D in water show enrichments from 0.39 to 0.69‰ and from 0.62 to 1.49‰ respectively. These values correspond to W/R ratios of 0.4–7. The distinct18O enrichments indicate that the isotopic composition of the oceans is not completely buffered by the hydrothermal circulations. The3He-enthalpy relationship is discussed in terms of both hydrothermal heat flux and3He mantle flux. 相似文献
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Snow samples were taken from a 5-m-deep pit located near the South Pole station in January 1975 and continuous deuterium, tritium and β activity profiles have been obtained from them. These three measurements and the stratigraphic observations allow us to deduce a precise chronology of the pit from 1950 to 1975, providing a continuous record of artificial tritium fallout in the southern hemisphere; this record has been extended to 1978 using samples from a second pit taken this last year. Taking advantage of the unusual 1957–1958 stable isotope content in the snow, we have demonstrated that an important part of the isotopic signal in the precipitation is retained in the snow in spite of the low accumulation rate (8.2 g cm?2 yr?1).The first artificial tritium, due to the 1952 Ivy experiments was detected during 1954. A two-year delay between explosions and fallout is well established and allows us to relate the tritium fallout to the main nuclear tests from 1952 to 1960. This delay appears longer for the large 1961–1962 devices. A stratospheric half residence time equal to 20 months is deduced from the fallout decrease occurring after the 1966 peak. For the French southern hemisphere experiments, it is about one year. A sharp tritium decrease is observed after a high 1973 peak, providing a new tritium reference level for future glaciological studies in Antarctica.The β and tritium peaks occur respectively during the Antarctic summer and the Antarctic winter, showing different injection mechanisms. This winter input and the high tritium values registered at the South Pole indicate a preferential tritium transfer over the pole area. Two mechanisms, stratospheric-tropospheric exchange and direct stratospheric cloud precipitation could account for this injection. 相似文献
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Primary ‘carbonic’ fluid inclusions filled with nearly pure high density CO2 occur in garnet in a garnet—biotite gneiss from ‘Système du Graphite’, Komajia, Madagascar (Malagasy). They have been formed during syntectonic growth of the garnet under granulite facies conditions. Most of the biotite appears to have crystallized later than the garnet under the influence of more water rich fluids. 相似文献
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Lucien Jeanmaire Michel Masson Francois Patti Pierre Germain Liliane Cappellini 《Marine pollution bulletin》1981,12(1):29-32
Analyses for 99Tc in some marine biological samples taken near the outlet of the low level radioactive effluent pipeline of the nuclear reprocessing plant of La Hague, France, gave positive results. From 500 to 3500 pCi kg?1 wet weight of 99Tc were observed in brown algae; Fucus sp. appeared to be a good indicator of this long-lived radionuclide in a marine environment. 相似文献