784 resultados para deep-water evolution
Resumo:
Two distinct hydrogeochemical regimes currently dominate the Peruvian continental margin. One, in shallower water (150-450 m) shelf to upper-slope regions, is characterized by interstitial waters with strong positive chloride gradients with depth. The maximum measured value of 1043 mM chloride at Site 680 at ITS corresponds to a degree of seawater evaporation of ~2 times. Major ion chemistry and strontioum isotopic composition of the interstitial waters suggest that a subsurface brine that has a marine origin and is of pre-early Miocene "age," profoundly influences the chemistry and diagenesis of this shelf environment. Site 684 at ~9°S must be closest to the source of this brine, which becomes diluted with seawater and/or interstitial water as it flows southward toward Site 686 at ~13?S (and probably beyond) at a rate of approximately 3 to 4 cm/yr, since early Miocene time. The other regime, in deep water (3000-5000 m) middle to lower-slope regions, is characterized by interstitial waters with steep negative and nonsteady-state chloride gradients with depth. The minimum measured value of 454 mM chloride, at Site 683 at ITS, corresponds to ~20% dilution of seawater chloride The most probably sources of these low-chloride fluids are gas hydrate dissociation and mineral (particularly clay) dehydration reactions. Fluid advection is consistent with (1) the extent of dilution shown in the chloride profiles, (2) the striking nonsteady-state depth profiles of chlorides at Sites 683 and 688 and of 87Sr/86Sr ratios at Site 685, and (3) the temperatures resulting from an average geothermal gradient of 50°C/km and required for clay mineral dehydration reactions. Strontium isotope data reveal two separate fluid regimes in this slope region: a more northerly one at Sites 683 and 685 that is influenced by fluids with a radiogenic continental strontium signature, and a southerly one at Sites 682 and 688 that is influenced by fluids with a nonradiogenic oceanic signatures. Stratigraphically controlled fluid migration seems to prevail in this margin. Because of its special tectonic setting, Site 679 at ITS is geochemically distinct. The interstitial waters are characterized by seawater chloride concentrations to -200 mbsf and deeper by a significantly lower chloride concentration of about two-thirds of the value in seawater, suggesting mixing with a meteoric water source. Regardless of the hydrogeochemical regime, the chemistry and isotopic compositions of the interstitial waters at all sites are markedly modified by diagenesis, particularly by calcite and dolomite crystallization.
Resumo:
The Southern Ocean is perhaps the only region where fluctuations in the global influence of North Atlantic Deep Water (NADW) can be monitored unambiguously in single deep-sea cores. A carbon isotope record from benthic foraminifera in a Southern Ocean core reveals large and rapid changes in the flux of NADW during the last deglaciation, and an abrupt increase in the NADW production rate which immediately preceded large-scale melting of the Northern Hemisphere ice sheets. This sudden strengthening of the NADW thermoha-line cell provides strong evidence for the importance of NADW in glacial-interglacial climate change.
Resumo:
Twenty-three sediment intervals from top of Site 650 down to 510 m below seafloor have been studied. Their thicknesses vary between 0.25 m and about 40 m. The studied deposits are turbidites or parts of them except one which is interpreted as an ash-fall layer. The composition of the turbidites signalizes sources from shallow water/coastal areas as well as from deep water levels. Repeated mobilization and displacement seems to have been common. Volcaniclastic material is the dominant component of the whole studied part of Site 650 sedimentary sequence. Ashfall deposits as well as normal open marine sediments are rare.
Resumo:
The volume presents planktological and chemical data collected during cruise No. 51 of RV "Meteor" to the equatorial Atlantic (FGGE '79) from February to June 1979. A standard section along the meridian 22° W across the equator was sampled ten times between 2° S and 3° N. Together with a temperature and salinity profile, concentrations of oxygen, nutrients and chlorophyll a were analyzed in water samples down to a depth of 250 m. Solar radiation and light depths were measured for determination of primary productivity of the euphotic zone according to the simulated in situ method. Zooplankton biomass was estimated in 5 depth intervals down to 300 m by means of a multiple opening and closing net equipped with a mesh size of 100 µm.
Resumo:
Despite its enormous extent and importance for global climate, the South Pacific has been poorly investigated in comparison to other regions with respect to chemical oceanography. Here we present the first detailed analysis of dissolved radiogenic Nd isotopes (epsilon-Nd) and rare earth elements (REEs) in intermediate and deep waters of the mid-latitude (~40°S) South Pacific along a meridional transect between South America and New Zealand. The goal of our study is to gain better insight into the distribution and mixing of water masses in the South Pacific and to evaluate the validity of Nd isotopes as a water mass tracer in this remote region of the ocean. The results demonstrate that biogeochemical cycling (scavenging processes in the Eastern Equatorial Pacific) and release of LREEs from the sediment clearly influence the distribution of the dissolved REE concentrations at certain locations. Nevertheless, the Nd isotope signatures clearly trace water masses including AAIW (Antarctic Intermediate Water) (average epsilon-Nd = -8.2 ± 0.3), LCDW (Lower Circumpolar Deep Water) (average epsilon-Nd = -8.3 ± 0.3), NPDW (North Pacific Deep Water) (average epsilon-Nd = -5.9 ± 0.3), and the remnants of NADW (North Atlantic Deep Water) (average epsilon-Nd = -9.7 ± 0.3). Filtered water samples taken from the sediment-water interface under the deep western boundary current off New Zealand suggest that boundary exchange processes are limited at this location and highlight the spatial and temporal variability of this process. These data will serve as a basis for the paleoceanographic application of Nd isotopes in the South Pacific.
Resumo:
In the course of the voyages 9a and 9c (1967) and 19 (1970) of the RV "Meteor" samples of plankton and neuston have been taken in the area of the Great Meteor Seamount. The euphausiids of this material have been examined quantitatively as well as qualitatively in order to study the influence of the Great and Small Meteor Seamount on a vertically migrating group of plankton. 20 species could be identified. All stem from the surrounding deep water and belong to the tropical and subtropical fauna. On the plateau of the Great Meteor Seamount no indigenous species have been encountered and also the typical neritic species from the west coast off Africa are lacking. As for the euphausiids no relationships exist between the Great Meteor Seamount and the shelf area of West Africa. The dominant species around the Meteor Seamount were Euphausia brevii, Stylocheiron suhmii, E. hemigibba, S. longicorne and Thysanopoda subaequalis. Using the index of diversity (Simpson) distinct differences in the composition of species could be shown to exist between the plateau area of the Meteor Seamount and the surrounding sea. On the plateau of the Great Meteor Seamount the number of species was only 7, E. brevis and S. suhmii dominated. None of the species occurred in great numbers and none is adapted to the specific environmental conditions of the plateau of the Meteor Seamount. The fauna of the plateau is a depauperate one as compared with that of the surrounding sea. This can be explained by the fact that adult euphausiids require for their existence greater water depths than are found above the plateau of the Meteor Seamount.
Resumo:
High-resolution, fish tooth Nd isotopic records for eight Deep Sea Drilling Project and Ocean Drilling Program sites were used to reconstruct the nature of late Paleocene-early Eocene deep-water circulation. The goal of this reconstruction was to test the hypothesis that a change in thermohaline circulation patterns caused the abrupt 4-5°C warming of deep and bottom waters at the Paleocene/Eocene boundary - the Paleocene-Eocene thermal maximum (PETM) event. The combined set of records indicates a deep-water mass common to the North and South Atlantic, Southern and Indian oceans characterized by mean epsilon-Nd values of ~-8.7, and different water masses found in the central Pacific Ocean (epsilon-Nd ~-4.3) and Caribbean Sea (epsilon-Nd ~1.2). The geographic pattern of Nd isotopic values before and during the PETM suggests a Southern Ocean deep-water formation site for deep and bottom waters in the Atlantic and Indian ocean basins. The Nd data do not contain evidence for a change in the composition of deep waters prior to the onset of the PETM. This finding is consistent with the pattern of warming established by recently published stable isotope records, suggesting that deep- and bottom-water warming during the PETM was gradual and the consequence of surface-water warming in regions of downwelling.
Resumo:
Middle/late Miocene to early Pliocene sedimentary sequences along the continental margin of southwest Africa have changes that correspond to the carbonate crash (12-9 Ma) and biogenic bloom events (~7-4 Ma) described in the equatorial Pacific by Farrell et al. (1995, doi:10.2973/odp.proc.sr.138.143.1995). To explore the origins of these changes, we analyzed the carbon and coarse fraction contents of sediments from ODP Sites 1085, 1086, and 1087 at a time resolution of 5 to 30 kyr. Several major drops in CaCO3 concentration between 12 and 9 Ma are caused by dilution from major increases in clastic input from the Oranje River during global sea level regressions. Abundant pyrite crystals and good preservation of fish debris reflect low oxygenation of bottom/pore waters. Regional productivity was enhanced during the time equivalent to the carbonate crash period. Higher benthic/planktic foraminiferal ratios indicate that CaCO3 dissolution at Site 1085 peaked between 9 to 7 Ma, which was after the global carbonate crash. This period of enhanced dissolution suggests that Site 1085 was located within a low-oxygen water mass that dissolved CaCO3 more easily than North Atlantic Deep Water, which began to bathe this site at 7 Ma. At 7 to 6 Ma, the onset of the biogenic bloom, increases and variations in total organic carbon and benthic foraminiferal accumulation rates show that paleoproductivity increased significantly above values observed during the carbonate crash period and fluctuated widely. We attribute the late Miocene paleoproductivity increase off southwest Africa to ocean-wide increases in nutrient supply and delivery.
Resumo:
Many marine radiogenic isotope records show both spatial and temporal variations, reflecting both the degree of mixing of distinct sources in the oceans and changes in the distribution of chemical weathering on the continents. However, changes in weathering and transport processes may themselves affect the composition of radiogenic isotopes released into seawater. The provenance of physically weathered material in the Labrador Sea, constrained through the use of Ar-Ar ages of individual detrital minerals, has been used to estimate the relative contributions of chemically weathered terranes releasing radiogenic isotopes into the Labrador Sea. A simple box-model approach for balancing observed Nd-isotope variations has been used to constrain the relative importance of localised input in the Labrador Sea, and the subsequent mixing of Labrador Sea Water into North Atlantic Deep-Water. The long-term pattern of erosion and deep-water formation around the North Atlantic seems to have been a relatively stable feature since 1.5 Ma, although there has been a dramatic shift in the nature of physical and chemical weathering affecting the release of Hf and Pb isotopes. The modelled Nd isotopes imply a relative decrease in water mass advection into the Labrador Sea between 2.4 and 1.5 Ma, accompanied by a decrease in the rate of overturning, possibly caused by an increased freshwater input into the Labrador Sea.
Resumo:
Oxygen and carbon isotope ratios in Eocene and Oligocene planktonic and benthic foraminifera have been investigated from Atlantic, Indian, and Pacific Ocean locations. The major changes in Eocene-Oligocene benthic foraminiferal oxygen isotopes were enrichment of up to 1 per mil in 18O associated with the middle/late Eocene boundary and the Eocene/Oligocene boundary at locations which range from 1- to 4-km paleodepth. Although the synchronous Eocene-Oligocene 18O enrichment began in the latest Eocene, most of the change occurred in the earliest Oligocene. The earliest Oligocene enrichment in 18O is always larger in benthic foraminifera than in surface-dwelling planktonic foraminifera, a condition that indicates a combination of deep-water cooling and increased ice volume. Planktonic foraminiferal d18O does not increase across the middle/late Eocene boundary at our one site with the most complete record (Deep Sea Drilling Project Site 363, Walvis Ridge). This pattern suggests that benthic foraminiferal d18O increased 40 m.y. ago because of increased density of deep waters, probably as a result of cooling, although glaciation cannot be ruled out without more data. Stable isotope data are averaged for late Eocene and earliest Oligocene time intervals to evaluate paleoceanographic change. Average d18O of benthic foraminifera increased by 0.64 per mil from the late Eocene to the early Oligocene d18O maximum, whereas the average increase for planktonic foraminifera was 0.52 per mil. This similarity suggests that the Eocene/Oligocene boundary d18O increase was caused primarily by increased continental glaciation, coupled with deep sea cooling by as much as 2°C at some sites. Average d18O of surface-dwelling planktonic foraminifera from 14 upper Eocene and 17 lower Oligocene locations, when plotted versus paleo-latitude, reveals no change in the latitudinal d18O gradient. The Oligocene data are offset by ~0.45 per mil, also believed to reflect increased continental glaciation. At present, there are too few deep sea sequences from high latitude locations to resolve an increase in the oceanic temperature gradient from Eocene to Oligocene time using oxygen isotopes.