977 resultados para ATLANTIC-OCEAN


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The high-resolution delta18O and delta13C records of benthic foraminifera from a 150,000-year long core from the Caribbean Sea indicate that there was generally high delta13C during glaciations and low delta13C during interglaciations. Due to its 1800-m sill depth, the properties of deep water in the Caribbean Sea are similar to those of middepth tropical Atlantic water. During interglaciations, the water filling the deep Caribbean Sea is an admixture of low delta13C Upper Circumpolar Water (UCPW) and high delta13C Upper North Atlantic Deep Water (UNADW). By contrast, only high delta13C UNADW enters during glaciations. Deep ocean circulation changes can influence atmospheric CO2 levels (Broecker and Takahashi, 1985; Boyle, 1988 doi:10.1029/JC093iC12p15701; Keir, 1988 doi:10.1029/PA003i004p00413; Broecker and Peng, 1989 doi:10.1029/GB003i003p00215). By comparing delta13C records of benthic foraminifera from cores lying in Southern Ocean Water, the Caribbean Sea, and at several other Atlantic Ocean sites, the thermohaline state of the Atlantic Ocean (how close it was to a full glacial or full interglacial configuration) is characterized. A continuum of circulation patterns between the glacial and interglacial extremes appears to have existed in the past. Subtracting the deep Pacific (~mean ocean water) delta13C record from the Caribbean delta13C record yields a record which describes large changes in the Atlantic Ocean thermohaline circulation. The delta13C difference varies as the vertical nutrient distribution changes. This new proxy record bears a striking resemblance to the 150,000-year-long atmospheric CO2 record (Barnola et al., 1987 doi:10.1038/329408a0). This favorable comparison between the new proxy record and the atmospheric CO2 record is consistent with Boyle's (1988a) model that vertical nutrient redistribution has driven large atmospheric CO2 changes in the past. Changes in the relative contribution of NADW and Pacific outflow water to the Southern Ocean are also consistent with Broecker and Peng's (1989) recent model for atmospheric CO2 changes.

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High resolution benthic oxygen isotope records combined with radiocarbon datings, from cores retrieved in the North, Equatorial, and South Atlantic are used to establish a reliable cronostratigraphy for the last 60 ky. This common temporal framework enables us to study the timing of the sub-Milankovitch climate variability in the entire surface Atlantic during this period, as reflected in planktonic oxygen isotope records. Variations in sea surface temperatures in the Equatorial and South Atlantic reveal two warm periods during the mid-stage 3 which are correlated to the warming observed in the North Atlantic after Heinrich events (HL) 5 and 4. However, the records show that the warming started about 1500 y earlier in the South Atlantic. A zonally averaged ocean circulation model simulates a similar north-south thermal antiphasing between the latitudes of our coring sites, when pertubated by a freshwater flux anomaly. We infer that the observed phase relationship between the northern and the southern Atlantic is related to periods of reduced NADW production in the North Atlantic, such as during HL5 and HL4.

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Application of quantitative micropaleontologic methods of sea-surface temperature (SST) estimation to the planktic foraminiferal faunas at Hole 548 in the northeast Atlantic between 3.5 and 2.0 Ma provide a detailed record of Pliocene surface temperature changes during the onset of major Northern Hemisphere glaciation. SST estimates indicate a relatively warm interval of "enhanced interglacials (warm peaks)" between 3.2 and 2.8 Ma followed by steady cooling with a significant step-like change toward colder temperatures occurring about 2.4 Ma. This record compares well with faunal and SST records from other North Atlantic sites.

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Mineral and chemical compositions of a set of crust samples collected from the North, Central and South Atlantic were examined by means of analytical electron microscopy and ICP-MS, chemical, and microchemical elemental analysis. Vernadite, asbolane, and goethite are dominant mineral phases of the crusts, ferrihydrite is minor, hematite and feroxyhyte are rare. The samples show wide variability in major and trace element contents; however, their characteristic geochemical signatures indicate hydrogenous origin. A comparison between compositions of oceanic hydrogenous and hydrothermal crusts and metalliferous hydrothermal sediments from different ocean areas suggests that the geochemical approach may be insufficient in some cases and fail to identify hydrothermal input in ferromanganese crusts of mixed composition.

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An original method of paleotemperature analysis on planktonic foraminifera is substantiated and actively used for stratigraphy of bottom sediments and paleoceanologic reconstructions. On the base of this method, as well as on lithological, geochemical, and oxygen isotope data, radiocarbon dating, constructions of other investigators, etc., the main features of dynamic Quaternary paleoceanology of the Atlantic Ocean is reconstructed. It is discussed in the context of global paleogeography. Paleotemperature field, climatic zonation, paleoecology of foraminifera, position of the main water masses, water fronts, currents, distribution of sea ice boundaries, upwelling activity, benthic circulation, processes of sedimentation are econstructed and analyzed.

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The aim of the present study is an evaluation of the applicability of biogenic barium as a proxy for productivity. For this purpose, 190 surface sediment samples from the South Atlantic Ocean were analysed for their barium and aluminium concentrations. Biogenic barium is estimated by subtracting the calculated terrigenous barium (obtained from the terrigenous Ba/Al ratio and the amount of Al in the sample) from the total Ba content in the sample. Based on the accumulation rates of biogenic barium, export production is estimated using three different algorithms proposed by [Paleoceanography 7 (1992) 163, doi:10.1029/92PA00181; Global Biogeochem. Cycles 9 (1995) 289, doi:10.1029/95GB00021; Geomar. Report 38 (1995) 105]. Primary productivity was calculated from these different export productions and compared with measurements of recent primary productivity in the overlying surface waters. Only the primary productions calculated on the basis of the algorithm of [Paleoceanography 7 (1992) 163, doi:10.1029/92PA00181] yield productivity values comparable to those existing in ocean surface waters. This study further reveals that it is not sufficient to use a constant, generally applicable organic carbon/biogenic barium ratio, as is postulated by [Global Biogeochem. Cycles 9 (1995) 289, doi:10.1029/95GB00021]. This ratio has to be assessed regionally. For the sediments of the Cape Basin in the eastern South Atlantic Ocean, a new algorithm is developed which gives plausible primary productivities for the overlying surface waters.

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One of the objectives of WHOI Atlantis Cruise 151, covering the period from 7 December 1947 to 18 June 1948, was to obtain as complete a sampling of the sea bottom of the Meditterranean and Aegean Seas as was compatible with the remainder of the scientific program. It was furthermore planned to make concurrent bottom photographs as a means for studying the correlation between bottom sediments and the morphology of the sea floor. The photographs also held the possibility of determining the presence of bottom fauna. The underwater camera used for this work was loaned to us by Dr. Maurice Ewing of Columbia University. As it was fitted with a one foot long coring tube at the base of its pole a majority of the bottom samples were obtained by the camera itself. On the way to Gibraltar, several bottom photos were taken in the Atlantic ocean. One of them was the deepest underwater photograph ever taken at the tima (3026 fathoms) showing a cluster of objects, some as much as 5 inches across on a clay bottom. These appeared to be manganese nodules, judging from their rounded and bulbous shape, especially the potato-like form of some of them. A core sample obtained at the same spot with a corer attached to the camera stand contained abundant manganese grains.

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Typical size of bubbles obtained from cavitation inception pressure measured in the surface layer of the Atlantic Ocean in situ aboard R/V Professor Vize in 1971 and Nerey in 1973 are reported. These results do not contradict ones of bubble size measurements using optical or acoustical techniques. Variability of bubble size is discovered and described. This variability is related to passing from one geographical region to another (from 68°55'S to 61°52'N), to changes in depth (from 5 to 100 m) and in day time, as well as to spatial fluctuations within an aquatic area. It is suggested that, in addition to wave breaking, there is another source of bubbles at depth 10-20 m that associates with hydrobiological processes.

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Phyric basalts recovered from DSDP Legs 45 and 46 contain abundant plagioclase phenocrysts which occur as either discrete single grains (megacrysts) or aggregates (glomerocrysts) and which are too abundant and too anorthitic to have crystallized from a liquid with the observed bulk rock composition. Almost all the plagioclase crystals are complexly zoned. In most cases two abrupt and relatively large compositional changes associated with continuous internal morphologic boundaries divide the plagioclase crystals into three parts: core, mantle and rim. The cores exhibit two major types of morphology: tabular, with a euhedral to slightly rounded outline; or a skeletal inner core wrapped by a slightly rounded homogeneous outer core. The mantle region is characterized by a zoning pattern composed of one to several spikes/plateaus superimposed on a gently zoned base line, with one large plateau always at the outside of the mantle, and by, in most cases, a rounded internal morphology. The inner rim is typically oscillatory zoned. The width of the outer rim can be correlated with the position of the individual crystal in the basalt pillow. The presence of a skeletal inner core and the concentration of glass inclusions in low-An zones in the mantle region suggest that the liquid in which these parts of the crystals were growing was undercooled some amount. The resorption features at the outer margins of low-An zones indicate superheating of the liquid with respect to the crystal. It is proposed that the plagioclase cores formed during injection of primitive magma into a previously existing magma chamber, that the mantle formed during mixing of a partially mixed magma and the remaining magma already in the chamber, and that the inner rim formed when the mixed magma was in a sheeted dike system. The large plateau at the outside of the mantle may have formed during the injection of the next batch of primitive magma into the main chamber, which may trigger an eruption. This model is consistent with fluid dynamic calculations and geochemically based magma mixing models, and is suggested to be the major mechanism for generating the disequilibrium conditions in the magma.

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Major element composition ranges of closely associated basalt glass-whole rock pairs from individual small cooling units approach the total known range of basalt glass and whole rock compositions at IPOD sites 417 and 418. The whole rock samples fall into two groups: one is depleted in MgO and distinctly enriched in plagioclase but has lost some olivine and/or pyroxene relative to its corresponding glass; and the other is enriched in MgO and in phenocrysts of olivine and pyroxene as well as plagioclase compared to its corresponding glass. By analogy with observed phenocryst distributions in lava pillows, tubes, and dikes, and with some theoretical studies, we infer that bulk rock compositions are strongly affected by phenocryst redistribution due to gravity settling, flotation, and dynamic sorting after eruption, although specific models are not well constrained by the one-dimensional geometry of drill core. Compositional trends or groupings in whole rock data resulting from such late-stage processes should not be confused with more fundamental compositional effects produced in deep chambers or during partial melting.

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