Carbon isotopes, hydrography, and nutrients measured at hydrographic stations from a transatlantic section near 40° N

14C concentrations, as well as 14C, hydrographic and nutrient data are reported for 5 hydrographic stations that form a transatlantic section near 40° N ("Meteor" cruise no. 23, 1971). Precision (for 14C ± 0.3 ? or better) and comparability with literature data are specified. A planned intercomparison with the US GEOSECS program within the Newfoundland Basin deep water failed because of variability of water characteristics. The observed 14C values decrease from about Delta 14C = + 80 ? at the surface to -70 ? at 2000 m depth. Deeper down, the values west of the Midatlantic Ridge remain similar, whereas those east of the ridge decrease further, to about - 110 ?. It is shown that bomb-14C is prominent down to about 1500 m depth. Beyond this depth the bomb 14C component is small and is negligible in the eastern basin below 2800 m. On the basis of the 14C-tritium correlation, the distribution of natural 14C below about 1500 m depth is derived from the observations. In the deep and bottom water east of the ridge the 14C-salinity relationship seemingly is non-linear. Contrary to expectation, the 14C concentration in the bottom water is not lower than found on an US GEOSECS station near 10° N. Apparently, lateral concentration differences in the Northeast Atlantic bottom water as well as nonlinearity of the 14C-salinity relationship at 40° N do not exceed 10 ? in Delta 14C.

Geochemistry of hydrothermal solutions, ores, and biota from hydrothermal fields at the East Pacific Rise axis near 9°50'N

Hydrothermal solutions were examined in a circulation system that started to develop after the 1991 volcanic eruption in the axial segment of the EPR between 9°45'N and 9°52'N. Within twelve years after this eruption, diffusion outflow of hot fluid from fractures in basaltic lavas gave way to focused seeps of hot solutions through channels of hydrothermal sulfide edifices. An example of the field Q demonstrates that from 1991 to 2003 H2S concentrations decreased from 86 to 1 mM/kg, and the Fe/H2S ratio simultaneously increased by factor 1.7. This fact can explain disappearance of microbial mats that were widespread within the fields before 1991. S isotopic composition of H2S does not depend on H2S concentration. This fact testifies rapid evolution of the hydrothermal system in the early years of its evolution. Carbon in CH4 from hot fluid sampled in 2003 is richer in 12C isotope than carbon in fluid from the hydrothermal field at 21°N EPR. It suggests that methane comes to the Q field from more than one source. Composition of particulate matter in hydrothermal solutions indicates that it was contributed by biological material. Experimental solutions with labeled substrates (t<70°C) show evidence of active processes of methane oxidation and sulfate reduction. Our results indicate that, during 12-year evolution of the hydrothermal system, composition of its solutions evolved and approached compositions of solutions in mature hydrothermal systems of the EPR.