172 resultados para temperature rise


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Bioaccumulation of trace metals in carbonate shells of mussels and clams was investigated at seven hydrothermal vent fields of the Mid-Atlantic Ridge (Menez Gwen, Snake Pit, Rainbow, and Broken Spur) and the Eastern Pacific (9°N and 21°N at the East Pacific Rise and the southern trough of Guaymas Basin, Gulf of California). Mineralogical analysis showed that carbonate skeletons of mytilid mussel Bathymodiolus sp. and vesicomyid clam Calyptogena m. are composed mainly of calcite and aragonite, respectively. The first data were obtained for contents of a variety of chemical elements in bivalve carbonate shells from various hydrothermal vent sites. Analyses of chemical compositions (including Fe, Mn, Zn, Cu, Cd, Pb, Ag, Ni, Cr, Co, As, Se, Sb, and Hg) of 35 shell samples and 14 water samples from mollusk biotopes revealed influences of environmental conditions and some biological parameters on bioaccumulation of metals. Bivalve shells from hydrothermal fields with black smokers are enriched in Fe and Mn by factor of 20-30 relative to the same species from the Menez Gwen low-temperature vent site. It was shown that essential elements (Fe, Mn, Ni, and Cu) more actively accumulated during early ontogeny of the shells. High enrichment factors of most metals (n x 100 - n x 10000) indicate efficient accumulation function of bivalve carbonate shells. Passive metal accumulation owing to adsorption on shell surfaces was estimated to be no higher than 50% of total amount and varied from 14% for Fe to 46% for Mn.

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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.

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The southernmost record of Maestrichtian pelagic carbonate sedimentation was recovered from ODP Leg 113 Holes 689B and 690C, drilled on the Maud Rise in the eastern Weddell Sea sector of the Southern Ocean (65°S). Well preserved and abundant planktonic foraminifers occur throughout Maestrichtian cores from both holes, providing a nearly complete biogeographic and biostratigraphic history of this region. Diversity is low compared to tropical and subtropical assemblages, with a maximum within sample diversity of 16 planktonic foraminifer species and a diversity total for the Maestrichtian of 24 species. The assemblages are dominated throughout by Heterohelix, Globigerinelloides, and a new species of Archaeoglobigerina, whereas keeled taxa are completely absent from the lower Maestrichtian and rare in the middle through upper Maestrichtian sediments. Three planktonic foraminifer species are described as new and are recognized as being endemic to the Austral Province. These include Archaeoglobigerina australis n. sp., Hedbergella sliteri n. sp., and Archaeoglobigerina mateola n. sp. The former two species were previously illustrated in reports on Late Cretaceous foraminifers from the Falkland Plateau and the northern Antarctic Peninsula. Two keeled and five non-keeled planktonic foraminifers, previously not found in high latitude Maestrichtian sediments, first appeared at the Maud Rise during the late early and late Maestrichtian. Correlation with their stratigraphic ranges in low latitude sequences shows that their first appearance datums are considerably younger at the Maud Rise than in the lower latitudes. The most likely explanation for this observation is that there was a warming in the south polar region during the late early and late Maestrichtian and a concomitant poleward migration of stenothermal taxa. However, oxygen isotopic paleotemperature results from Sites 689 and 690 (Barrera and Huber, 1990, doi:10.2973/odp.proc.sr.113.137.1990) show a long-term cooling trend throughout the Maestrichtian, indicating that other factors may have played a more important role than temperature in the distribution of Maestrichtian planktonic foraminifers. A new biostratigraphic scheme is proposed for the Antarctic because of the absence of thermophilic planktonic foraminifers used to identify existing low to middle latitude zones. The Globigerinelloides impensus Partial Range Zone is defined for the late Campanian-Maestrichtian, the Globotruncanita havanensis Partial Range Zone is redefined for the early to late early Maestrichtian, and the Abathomphalus mayaroensis Total Range Zone is recognized. Good quality magnetic polarity data obtained from both Maud Rise sites (Hamilton, 1990, doi:10.2973/odp.proc.sr.113.179.1990) enables magnetobiostratigraphic correlation of twelve foraminifer datums with the geomagnetic polarity time scale of Haq et al. (1987). The geochronology thus obtained is crucial for accurate cross-latitudinal correlation and interpretation of the paleoceanographic history of the Antarctic region during the Maestrichtian time period.

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We measured oxygen-isotope compositions of 16 siliceous rocks from Deep Sea Drilling Project Sites 463, 464, 465, and 466 (Leg 62). Samples are from deposits that range in age from about 40 to 103 m.y. and that occur at sub-bottom depths of 9 to 461 meters. Mean d18O values range from 28.4 to 36.8 per mil and 36.0 ± 0.3 per mil for quartz-rich and opal-CTrich rocks, respectively. d18O values in chert decrease with increasing sub-bottom depth; the slope of the d18O/depth curve is less steep for Site 464 than for the other sites which indicates that chert at Site 464 formed at higher temperatures than chert at Sites 463, 465, and 466. Temperatures of formation of cherts were 7 to 42°C, using the silica-water fractionation factor of Knauth and Epstein (1976), or 19 to 56°C, using the equation of Clayton et al. (1972). Temperatures in the sediment where the cherts now occur are lower than their isotopically determined temperatures of formation, which means that the cherts record an earlier history when temperatures in the sediment section were greater. Estimated sediment temperatures when the cherts formed are comparable to, but generally slightly lower than, those calculated from Knauth and Epstein's equation. The isotopic composition of cherts is more closely related to environment of formation (diagenetic environment) or paleogeothermal gradients, than to paleoclimates (bottom-water temperatures). Opal-CT-rich rocks may better record paleo-bottom-water temperature. In Leg 62 cherts, better crystallinity of quartz corresponds to lower d18O values; this implies progressively higher temperatures of equilibration between quartz and water during maturation of quartz. The interrelationship of d18O and crystallinity is noted also in continental-margin deposits such as the Monterey Formation - but for higher temperatures. The apparent temperature difference between open-ocean and continental-margin deposits can be explained by the dominant control of temperature on silica transformation in the rapidly deposited continental-margin deposits, whereas time, as well as temperature, has a strong influence on the transformations in open-ocean deposits. Comparisons between the chemistry and d18O values of cherts reveal two apparent trends: both boron and SiO2 increase as d18O increases. However, the correspondence between SiO2 and d18O is only apparent, because the two cherts lowest in SiO2 are also the most deeply buried, so the trend actually reflects depth of burial. The correspondence between boron and d18O supports the conclusion that boron is incorporated in the quartz crystal structure during precipitation