Carbonate dissolution in the South Atlantic Ocean: evidence from ultrastructure breakdown in Globigerina bulloides

Ultrastructure dissolution susceptibility of the planktic foraminifer Globigerina bulloides, carbonate ion content of the water column, calcium carbonate content of the sediment surface, and carbonate/carbon weight percentage ratio derived from sediment surface samples were investigated in order to reconstruct the position of the calcite saturation horizon, the sedimentary calcite lysocline, and the calcium carbonate compensation depth (CCD) in the modern South Atlantic Ocean. Carbonate ion data from the water column refer to the GEOSECS locations 48, 103, and 109 and calcium carbonate data come from 19 GeoB sediment surface samples of 4 transects into the Brazil, the Guinea, and the Cape Basins. We present a new (paleo-) oceanographic tool, namely the Globigerina bulloides dissolution index (BDX). Further, we give evidence (a) for progressive G. bulloides ultrastructural breakdown with increasing carbonate dissolution even above the lysocline; (b) for a sharp BDX increase at the sedimentary lysocline; and (c) for the total absence of this species at the CCD. BDX puts us in the position to distinguish the upper open ocean and the upwelling influenced continental margin above from the deep ocean below the sedimentary lysocline. Carbonate ion data from water column samples, calcite weight percentage data from surface sediment samples, and carbonate/carbon weight percentage ratio appear to be good proxies to confirm BDX. As shown by BDX both the calcite saturation horizon (in the water column) and the sedimentary lysocline (at the sediment–water interface) mark the boundary between the carbonate ion undersaturated and highly corrosive Antarctic Bottom Water and the carbonate ion saturated North Atlantic Deep Water (NADW) of the modern South Atlantic.     

Surface sediment carbonate mineralogy and water column chemistry: Nicaragua Rise versus the Bahamas

Periplatform surface sediments were studied for carbonate mineralogy in conjunction with analyses of the water column for carbonate chemistry on the eastern Northern Nicaragua Rise (NNR) in the Caribbean Sea. The results show a strong correspondence between variations and disappearance, with increasing water depth, of metastable carbonate minerals (fine aragonite and magnesian calcite) and their respective saturation levels in the overlying waters. Similar correspondence between variations in sediment proportions of fine aragonite and magnesian calcite and their respective saturation levels has previously been established in the Bahamas. There are, however, significant differences between the two areas. The sharp decrease in aragonite content and the measured aragonite saturation level occur at 4000 m in the Bahamas, compared to 1800 m on the eastern NNR. In both areas, magnesian calcite minima correspond to the in situ PCO₂ maxima in the water column. The magnesian calcite minimum, however, is at 950 m in the Bahamas and 750 m on the eastern NNR. Magnesian calcite disappears in the Bahamas at 3800 m and at 2000 m on the eastern NNR. These results demonstrate the importance of the influence of overlying water chemistry on the preservation of metastable carbonate minerals in off-bank periplatform sediments, and they clearly demonstrate the difference in terms of carbonate preservation between the poorly ventilated waters of the Caribbean Sea and the well-oxygenated waters of the adjacent Atlantic Ocean. They also open the possibility of obtaining paleoceanographic information on the depth of the CO₂ maximum (O₂ minimum) and its separation from the aragonite saturation depth in at least some areas.     

Characterising the intermediate depth waters of the Pacific Ocean using δ13C and other geochemical tracers

Evidence from geochemical tracers (salinity, oxygen, silicate, nutrients, alkalinity, dissolved inorganic carbon (DIC), carbon isotopes (δ¹³C_DIC) and radiocarbon (Δ¹⁴C)) collected during the Pacific Ocean World Ocean Circulation Experiment (WOCE) voyages (P10, P15, P17 and P19) indicate there are three main water types at intermediate depths in the Pacific Ocean; North Pacific Intermediate Water (NPIW), Antarctic Intermediate Water (AAIW) and Equatorial Pacific Intermediate Waters (EqPIW). We support previous suggestions of EqPIW as a separate equatorial intermediate depth water as it displays a distinct geochemical signature characterised by low salinity, low oxygen, high nutrients and low Δ¹⁴C (older radiocarbon). Using the geochemical properties of the different intermediate depth waters, we have mapped out their distribution in the main Pacific Basin.From the calculated pre-formed δ¹³C_air–sea conservative tracer, it is evident that EqPIW is a combination of AAIW parental waters, while quasi-conservative geochemical tracers, such as radiocarbon, also indicate mixing with old upwelling Pacific Deep Waters (PDW). The EqPIW also displays a latitudinal asymmetry in non-conservative geochemical tracers and can be further split into North (NEqPIW) and South (SEqPIW) separated at ～2°N. The reason for this asymmetry is caused by higher surface diatom production in the north driven by higher silicate concentrations.The δ¹³C signature measured in benthic foraminifera, Cibicidoides spp. (δ¹³C_Cib), from four core tops bathed in AAIW, SEqPIW and NPIW, reflects that of the overlying intermediate depth waters. The δ¹³C_Cib from these cores show similarities and variations down-core that highlight changes in mixing over the last 30,000 yr BP. The reduced offset between the δ¹³C_Cib of AAIW and SEqPIW during the last glacial indicates that AAIW might have had an increased influence in the eastern equatorial Pacific (EEP) region at this time. Additional intermediate depth cores and other paleo-geochemical proxies such as Cd/Ca and radiocarbon are required from the broader Pacific Ocean to further understand changes in intermediate depth water formation, circulation and mixing over glacial/interglacial cycles.     

Dianeutral mixing,transformation and transport of Antarctic Intermediate Water in the South Atlantic Ocean

Recently obtained World Ocean Circulation Experiment (WOCE) sections combined with a specially prepared pre-WOCE South Atlantic data set are used to study the dianeutral (across neutral surface) mixing and transport achieving Antarctic Intermediate Water (AAIW) being transformed to be part of the North Atlantic Deep Water (NADW) return cell. Five neutral surfaces are mapped, encompassing the AAIW from 700 to 1100 db at the subtropical latitudes.Coherent and significant dianeutral upwelling is found in the western boundary near the Brazil coast north of the separation point (about 25°S) between the anticyclonic subtropical and cyclonic south equatorial gyres. The magnitude of dianeutral upwelling transport is 10^-3 Sv (1 Sv=10⁶ m³ s^-1) for 1°×1° square area. It is found that the AAIW sources from the southwestern South Atlantic and southwestern Indian Ocean do not rise significantly into the Benguela Current. Instead, they contribute to the NADW return formation by dianeutral upwelling into the South Equatorial Current. In other words, the AAIW sources cannot obtain enough heat/buoyancy to rise until they return to the western boundary region but north of the separation point. The basin-wide integration of dianeutral transport shows net upward transports, ranging from 0.25 to 0.6 Sv, across the lower and upper boundary of AAIW north of 40°S. This suggests that the equatorward AAIW is a slow rising water on a basin average. Given one order of uncertainty in evaluating the along-neutral-surface and dianeutral diffusivities from the assumed values, K=10³ m² s^-1 and D=10^-5 m² s^-1, the integrated dianeutral transport has an error band of about 10–20%. The relatively weak integrated dianeutral upwelling transport compared with AAIW in other oceans implies much stronger lateral advection of AAIW in the South Atlantic.Mapped Turner Angle in diagnosing the double-diffusion processes shows that the salty Central Water can flux salt down to the upper half of AAIW layer through salt-fingering. Therefore, the northward transition of AAIW can gain salt either through along-neutral-surface advection and diffusion or through salt fingering from the Central Water and heat through either along-neutral-surface advection and diffusion or dianeutral upwelling. Cabbeling and thermobaricity are found significant in the Antarctic frontal zone and contribute to dianeutral downwelling with velocity as high as −1.5×10^-7 m s^-1. A schematic AAIW circulation in the South Atlantic suggests that dianeutral mixing plays an essential role in transforming AAIW into NADW return formation.     

环南澳大利亚太平洋-印度洋海洋间南极中层水环流

On the basis of the salinity distribution of isopycnal(σ_0=27.2 kg/m~3) surface and in salinity minimum, the Antarctic Intermediate Water(AAIW) around South Australia can be classified into five types corresponding to five regions by using in situ CTD observations. Type 1 is the Tasman AAIW, which has consistent hydrographic properties in the South Coral Sea and the North Tasman Sea. Type 2 is the Southern Ocean(SO) AAIW, parallel to and extending from the Subantarctic Front with the freshest and coldest AAIW in the study area. Type 3 is a transition between Type 1 and Type 2. The AAIW transforms from fresh to saline with the latitude declining(equatorward). Type 4, the South Australia AAIW, has relatively uniform AAIW properties due to the semienclosed South Australia Basin. Type 5, the Southeast Indian AAIW, progressively becomes more saline through mixing with the subtropical Indian intermediate water from south to north. In addition to the above hydrographic analysis of AAIW, the newest trajectories of Argo(Array for real-time Geostrophic Oceanography) floats were used to constructed the intermediate(1 000 m water depth) current field, which show the major interocean circulation of AAIW in the study area. Finally, a refined schematic of intermediate circulation shows that several currents get together to complete the connection between the Pacific Ocean and the Indian Ocean. They include the South Equatorial Current and the East Australia Current in the Southwest Pacific Ocean, the Tasman Leakage and the Flinders Current in the South Australia Basin, and the extension of Flinders Current in the southeast Indian Ocean.     

Foraminiferal shell-weight evidence for sedimentary calcite dissolution above the lysocline

Shell-weight measurements were carried out on planktonic foraminifera G. sacculifer and G. ruber specimens from coretop depth transects in the Atlantic, Indian and Pacific Ocean to investigate calcite dissolution above the lysocline. The results suggest that foraminifera deposited in sediments overlain by supersaturated bottom water undergo considerable dissolution at the sediment–water interface and that the calcite saturation state at the interface is considerably offset from that of bottom water. Also, the extent of exposure to undersaturated conditions at the interface is not constant. Rather, it increases towards the surface ocean, i.e. towards shallow marine sediments where the organic matter flux is expected to be higher. It is proposed that the benthic fluff layer at the sediment–water interface represents a zone of undersaturation through which the foraminifera pass prior to deeper burial, and that the residence time of foraminifera within this zone of intense organic matter respiration is long enough to result in significant decreases in shell weight.     

South Atlantic and benthic foraminifer δ13C deviations: implications for reconstructing the Late Quaternary deep-water circulation

Benthic foraminifer species Cibicidoides wuellerstorfi and related genera are assumed to secrete calcite very close to the carbon isotope values of the ambient bottom-water ΣCO₂. Recently, attention has been focused on substantial productivity-linked δ¹³C depletions. To examine further the productivity effect on benthic δ¹³C deviations, we present data from the South Atlantic between 15 and 35°S, including water samples from 10 hydrographic stations and related surface-sediment measurements on C. wuellerstorfi. We compare open-ocean data with observations in the Namibia Upwelling area. As a result, δ¹³C_ΣCO2 values as well as phosphate concentrations in water samples of the upwelling realm differ significantly from those of the open-ocean realm at least in the upper and mid-depth water masses (SACW, AAIW, UCDW). However, deviations from the Redfield fractionation, caused by air–sea fractionation, remain constant within each water mass, which means that the carbon isotope changes toward upwelling areas are exclusively determined by biological cycling. In addition to lower δ¹³C_ΣCO2 values in upwelling areas, a depletion in the δ¹³C of epibenthic foraminifer calcite is observed, which is most likely explained by the decay of organic matter, reducing the ¹³C/¹²C ratio in the pore water and influencing the carbon isotopic composition of the C. wuellerstorfi shells of highly productive areas. The paleoceanographic implication of this effect for reconstructing the Late Quaternary deep-water circulation is discussed using carbon isotope records of several sediment cores within and outside the Namibia upwelling area.     

Origins and pathways of the subsurface and intermediate water masses of the Indonesian Throughflow derived from historical and Argo data

On the basis of Argo data and historic temperature/salinity data from the World Ocean Database 2001 （ WOD01 ）, origins and spreading pathways of the subsurface and intermediate water masses in the Indonesian Throughflow （ITF） region were discussed by analyzing distributions of salinity on representative isopyenal layers. Results were shown that, subsurface water mostly comes from the North Pacific Ocean while the intermediate water originates from both the North and South Pacific Ocean, even possibly from the Indian Ocean. Spreading through the Sulawesi Sea, the Makassar Strait, and file Flores Sea, the North Pacific subsurface water and the North Pacific Intermediate water dominate the western part of the Indonesian Archipelago. Furthermore as the depth increases, the features of the North Pacific sourced water masses become more obvious. In the eastern part of the waters, high sa- linity South Pacific subsurface water is blocked by a strong salinity front between Halmahera and New Guinea. Intermediate water in the eastern interior region owns salinity higher than the North Pacific intermediate water and the antarctic intermediate water （ AAIW）, possibly coming from the vertical mixing between subsurface water and the AAIW from the Pacific Ocean, and possibly coming from the northward extending of the AAIW from the Indian Ocean as well.     

Nannoplankton of the Atlantic Ocean from sediment trap samples

Calcareous nannoplankton from sediment trap samples collected at six sites in the Atlantic Ocean from 23° S to 73° N (cruise 20 of R/V Vityaz’ and cruise 33 and 34 of R/V Akademik Mstislav Keldysh). Those samples were studied with a scanning electron microscope. In the coastal and open-sea regions of the North and South Atlantic and in the subarctic region of the Norwegian Sea, the conditions are significantly different. In the shelf area of the Benguela upwelling, 11 species were recognized; some of them were agglutinated by diatoms and tintinnides or covered the surface of pellets. The Broken Spur and TAG pelagic areas of the North Atlantic contained up to 43 coccolith species. They included holococcoliths, large pelagic, and delicate easily soluble species distributed over the entire water column. The presence of coccoliths in the high-latitude area of the Norwegian Sea is related to their supply with the warmer North Atlantic waters. These assemblages are distinguished by a low species diversity and an enhancement of the coccolith solubility with the depth increase.     

Sources and distribution of fresh water in the East Greenland Current

Fresh water flowing from the Arctic Ocean via the East Greenland Current influences deep water formation in the Nordic Seas as well as the salinity of the surface and deep waters flowing from there. This fresh water has three sources: Pacific water (relatively fresh cf. Atlantic water), river runoff, and sea ice meltwater. To determine the relative amounts of the three sources of fresh water, in May 2002 we collected water samples across the East Greenland Current in sections from 81.5°N to the Irminger Sea south of Denmark Strait. We used nitrate-phosphate relationships to distinguish Pacific waters from Atlantic waters, salinity to obtain the sum of sea ice melt water and river runoff water, and total alkalinity to distinguish the latter. River runoff contributed the largest part of the total fresh water component, in some regions with some inventories exceeding 12 m. Pacific fresh water (Pacific source water S ∼ 32 cf. Atlantic source water S ∼ 34.9) typically provided about 1/3 of the river runoff contribution. Sea ice meltwater was very nearly non-existent in the surface waters of all sections, likely at least in part as a result of the samples being collected before the onset of the melt season. The fresh water from the Arctic Ocean was strongly confined to near the Greenland coast. We thus conjecture that the main source of fresh water from the Arctic Ocean most strongly impacting deep convection in the Nordic Seas would be sea ice as opposed to fresh water in the liquid phase, i.e., river runoff, Pacific fresh water, and sea ice meltwater.     

Seasonal export and sediment preservation of diatomaceous, foraminiferal and organic matter mass fluxes in a trophic gradient across the SE Atlantic

Seasonal deposition fluxes of sinking phytoplankton, zooplankton and major mass compounds (i.e. calcium carbonate, biogenic opal and organic matter), intercepted by deep-moored sediment traps, are contrasted with their sediment accumulation rates over the 2700 m deep central Walvis Ridge in the oligotrophic SE Atlantic. These data provide the first seasonally resolved record of biogenic particle fluxes in the South Atlantic Central Gyre and serve as the oligotrophic end member of a gradient across the Benguela system to the highly productive coastal upwelling off Namibia. Maximum fluxes at the central Walvis Ridge were deposited in early austral spring, following winter deepening of the surface mixed layer and associated nutrient entrainment. Nearly 25% of the annual mass flux arrived in October, when sea surface temperature rose, deep vertical mixing halted and surface production collapsed. The annual flux of diatoms was dominated by small specimens of Nitzschia bicapitata (60%) whereas Globorotalia inflata dominated the foraminiferal fluxes (25%). Diatom diversity dropped significantly during the bloom periods, when up to 80% was composed of small N. bicapitata, but foraminiferal diversity remained about constant. The diatom flux maximum, together with those of biogenic silica and organic matter, preceded those of the foraminifera, pteropods, carbonate and total mass by 1 week. Fluxes of the left- and right-coiled shells of the deep-dwelling foraminifer Globorotalia truncatulinoides peaked in different seasons, a distinctive ecological behaviour which merits their taxonomic recognition as separate species. These findings testify to recent evidence for the existence of several genetic species within G. truncatulinoides and now suggest that such species may also have different seasonal responses.The Benguela trophic gradient showed a shoreward increase in particle fluxes, but differences were surprisingly small, testifying to only moderately enhanced export productivity and deposition at the Namibian margin relative to the oligotrophic central gyre. From the open ocean toward coastal upwelling, small and weakly silicified diatoms were substituted by other, larger and more heavily silicified species, possibly in response to decreased silica limitation. Foraminiferal deposition fluxes were increasingly dominated by G. inflata, accompanied by a change-over from many warm- to few cold-water minor species. The late winter maximum at the Namibian margin and the early spring maximum at the central Walvis Ridge were generated by the same process of collapsing surface productivity in response to the shut down of nutrient entrainment at the winter to summer transition, although delayed by up to 2 months in the Central Gyre. At the sediment-water interface, intense degradation of organic matter and biogenic silica resulted in poor preservation accompanied by pronounced changes in the species composition of siliceous phytoplankton. Of all particle groups at the central Walvis Ridge, only the export of foraminiferal shells appeared to be fully transferred into the sediment, and through their species assemblage to provide a sedimentary record of past seasonal productivity conditions of the upper ocean.     

Occurrence of an exceptional carbonate dissolution episode during early glacial isotope stage 6 in the Southeastern Atlantic

Concentration and mass accumulation rate profiles from Southeastern Atlantic sediment cores located off Namibia show that an exceptional episode in benthic carbonate dissolution occurred during early glacial isotope stage 6 (substages 6.6 and 6.5) between about 186 000 and 170 000 yr BP. Although this episode is restricted to or is more pronounced in this region than in other areas of the Atlantic Ocean, its exceptional character with respect to older and younger climatic episodes at the same site cannot be fully explained by local factors alone, but requires a combination of local and global influences. The onset of the carbonate dissolution episode is related to a more efficient transfer of organic matter from surface eutrophic areas to the lower and is due to low sea level, while its termination relates to a change in either global ocean alkalinity or bottom water circulation. An evaluation of the magnitude of this local carbonate dissolution episode suggests that its contribution to a global alkalinity change may have been significant. Carbonate dissolution was probably amplified by stronger upwelling activity of the Benguela System linked to an exceptional northern excursion of the boreal summer ITCZ during early glacial isotope stage 6. This low latitude global linkage may explain how this carbonate dissolution event as well as other ‘anomalies’ observed for early stage 6, like an important Dole effect minimum or a ‘cold’ Mediterranean sapropel, are related.     

Glacial–interglacial variability in lower North Atlantic deep water: inference from silt grain-size analysis and carbonate preservation in the western equatorial Atlantic

Grain-size records of the terrigenous and calcareous silt fraction, preservation of planktic foraminifera, and benthic foraminiferal stable-isotope data (δ¹³C, δ¹⁸O values of C. wuellerstorfi) at ODP Site 927 on the Ceará Rise (5°27.7′N, 44°28.8′W), are used to reconstruct variations in the history of bottom current strength, ventilation, and carbonate corrosiveness of deep waters during the time interval from 0.8 to 0.3 Ma. Glacial periods are characterized by generally smaller mean sizes of the terrigenous sortable silt fraction (mean_(SS)), lower δ¹³C values, and poorer preservation of planktic foraminifera compared to interglacials. This indicates lower bottom current speeds, larger nutrient contents and more corrosive deep water. By contrast, larger mean_(SS) sizes, higher δ¹³C values, and well preserved planktic foraminifera indicate strong circulation and a well ventilated deep-water mass during interglacials. The observed changes are most likely related to the weakening and strengthening of circulation of Lower North Atlantic Deep Water (LNADW). Cross-spectral analysis between the mean_(SS) and benthic δ¹⁸O records reveals that minima in mean_(SS) occur about 7.6 k.y. after the maximum in ice volume. This indicates a considerable lag time between ice-shield induced changes in LNADW production and subsequent changes in the velocity of LNADW flow in the western equatorial Atlantic. Striking changes in bottom current speed occur regularly during glacial to interglacial transitions. Extremely fine mean_(SS) minima point to an almost complete shutdown of bottom current vigor in response to a cessation of LNADW production caused by an enhanced melt water release during the initial phases of deglaciation. However, each of the fine minima extremes is followed by a rapid shift to very high mean_(SS) values that indicate strong bottom currents, and hence, vigorous LNADW flow during the early interglacials. After the onset of glacial Stage 12, generally poorer carbonate preservation and higher variability is registered. This coincides with a global decrease in carbonate preservation during the mid-Brunhes (mid-Brunhes dissolution event). Detailed grain-size analysis of the calcareous fine fraction (<63 μm) revealed a considerable reduction of particles in the fraction from 7 to 63 μm during periods of enhanced dissolution. This indicates a preferential dissolution of larger planktic foraminiferal fragments which leads to an enrichment of coccoliths in the calcareous fine fraction.     

Kinematic elements of Antarctic Intermediate Water in the western South Atlantic

The northward flowing Antarctic Intermediate Water (AAIW) is a major contributor to the large-scale meridional circulation of water masses in the Atlantic. Together with bottom and thermocline water, AAIW replaces North Atlantic Deep Water that penetrates into the South Atlantic from the North. On the northbound propagation of AAIW from its formation area in the south-western region of the Argentine Basin, the AAIW progresses through a complex spreading pattern at the base of the main thermocline. This paper presents trajectories of 75 subsurface floats, seeded at AAIW depth. The floats were acoustically tracked, covering a period from December 1992 to October 1996. Discussions of selected trajectories focus on mesoscale kinematic elements that contribute to the spreading of AAIW. In the equatorial region, intermittent westward and eastward currents were observed, suggesting a seasonal cycle of the AAIW flow direction. At tropical latitudes, just offshore the intermediate western boundary current, the southward advection of an anticyclonic eddy was observed between 5^°S and 11°S. Farther offshore, the flow lacks an advective pattern and is governed by eddy diffusion. The westward subtropical gyre return current at about 28°S shows considerable stability, with the mean kinetic energy to eddy kinetic energy ratio being around one. Farther south, the eastward deeper South Atlantic Current is dominated by large-scale meanders with particle velocities in excess of 60 cm s^-1. At the Brazil–Falkland Current Confluence Zone, a cyclonic eddy near 40°S 50°W seems to act as injector of freshly mixed AAIW into the subtropical gyre. In general, much of the mixing of the various blends of AAIW is due to the activity of mesoscale eddies, which frequently reoccupy similar positions.     

Optimum multiparameter analysis of the water mass structure in the Atlantic Ocean thermocline

An analysis of the water mass structure of the Atlantic Ocean central layer is conducted by applying optimum multiparameter (OMP) analysis to an expansive historical data set. This inverse method utilises hydrographic property fields to determine the spreading and mixing of water masses in the permanent thermocline. An expanded form of OMP analysis is used, incorporating Redfield ratios and pseudo-age to correct for the non-conservative behaviour of oxygen and nutrients over large oceanic areas.Three water masses are considered to contribute to the central layer of the Atlantic Ocean. One of these is formed in each hemisphere of the Atlantic Ocean and the other advects around the southern tip of Africa from its formation region in the Indian Ocean. The Atlantic Ocean is analysed on a fine three-dimensional grid so that at every grid point the relative contributions of each water mass and the pseudo-age are determined.The model is remarkably successful in verifying many accepted circulation features in the Atlantic Ocean, including the large-scale circulations of the subtropical gyres, the zonal flows of equatorial currents at the equator, and a cross-equatorial flow of the water masses formed in the southern hemisphere near the western boundary. The inter-hemisphere flow is so important that almost half of the thermocline waters in the Caribbean Sea and the Gulf of Mexico are supplied by the two water masses formed in the South Atlantic and Indian Oceans. This provides support for an upper-layer replacement path for the formation of North Atlantic Deep Water. Further east, the sharp front at about 15°N between North and South Atlantic Central Waters is clearly discriminated throughout the thermocline. The central waters of the South Atlantic thermocline are found to be highly stratified, with central water formed in the Indian Ocean underlying the South Atlantic Central Water. At around 5°N a strong upwelling zone is identified in which the central water formed in the Indian Ocean penetrates towards the surface. The pseudo-age results allow pathways for the flow of water masses to be inferred, and clearly identify circulation features such as the subtropical gyres, the Equatorial Undercurrent, and the shadow zones in the eastern equatorial regions of the Atlantic Ocean. Water mass renewal in these shadow zones occurs on considerably longer time scales than for the well-ventilated subtropical gyres.     

Distribution of dissolved molybdenum,uranium and vanadium in baltic sea waters

This study presents dissolved molybdenum, uranium and vanadium profiles from eight stations in the main Baltic subregions. The elements were analysed by a new analytical procedure based on total-reflection X-ray fluorescence (TXRF). Mo and U reveal a strong, positive correlation with salinity (with r = 0.95 and 0.93, respectively). The estimated end-member concentrations (for S = 35 × 10^?3) are consistent with North Atlantic Ocean water values, indicating conservative mixing with Baltic river waters as the dominating process. In contrast, dissolved V shows relatively low levels, with mean surface and deep layer values of 2.7 and 1.7 nmol kg^?1, respectively. Compared with recently investigated Atlantic Ocean waters (normalized to S = 35 × 10^?3), Baltic waters are deplated in dissolved V by more than 60%. The removal is attributed to scavenging processes by terrigenous and/or biogenic material during the course of mixing. However, the data did not indicate that precipitation or other removal processes were significant in the anaerobic waters.     

基于历史资料和Argo资料的印尼贯通流次表层和中层水起源与路径探讨

利用Argo资料和《世界海洋数据集2001版》(WOD01)温盐历史资料,通过对代表性等位势面上盐度分布的分析,探讨了次表层和中层等不同层次上印尼贯通流(ITF)的起源与路径问题.分析结果表明,ITF的次表层水源主要来自北太平洋,中层水源地既包括北太平洋、南太平洋,同时也不能排除有印度洋的可能性.在印度尼西亚海域西部,ITF的次表层和中层水源分别为北太平洋热带水(NPTW)和中层水(NPIW),经苏拉威西海、望加锡海峡到达弗洛勒斯海,层次越深特征越明显.在印度尼西亚海域东部,发现哈马黑拉-新几内亚水道附近存在次表层强盐度锋面,阻隔了南太平洋热带水(SPTW)由此进入ITF海域;中层水具有高于NPIW和来自南太平洋的南极中层水(AAIW)的盐度值,既可能是AAIW和SPTW在当地发生剧烈垂直混合而形成,也可能是来自印度洋的AAIW向北延伸进入ITF的结果.     

δ13C analyses of oceanic particulate organic matter

Seventy-nine δ¹³C analyses of oceanic particulate matter (> 0·μ) from semi-tropical (Gulf of Mexico, Caribbean and Atlantic) and polar (South Indian Ocean) waters showed that the carbon isotope composition of the particulate matter from the cold polar surface waters was lighter ($\text{?24·7}\text{to}\text{?26·0‰}$) than that from the surface in the semi-tropical regions ($\text{?19·8}\text{to}\text{?22·3 ‰}$), reflecting the temperature effect on the photosynthetic fixation of carbon. δ¹³C for deep samples (> 330 m) were generally more negative than the surface samples, except in some well-mixed polar areas.A difference both in organic carbon isotopic composition and percentage organic carbon in the POM and the tops of sediment cores was also apparent; a loss of approximately 95 % of incoming carbon and an increase in ¹³C of several per mille being observed during deposition of particulate matter. This indicates that after settling on the bottom there is extensive diagenesis of the POM by organisms, indicating the non-refractory nature of the organic matter.     

The solid state speciation of copper in surface water particulates and oceanic sediments

A sequential leaching technique has been used to characterize the solid state speciation of total copper (∑Cu) among a number of operationally defined host fractions in surface seawater particulates from the Atlantic Ocean, a diagenetically active hemipelagic sediment core from the eastern Mediterranean, a turbidite - rich sediment core from the Madeira Abyssal Plain and a series of 79 Atlantic Ocean surface or near surface sediments. Around 50% of the ∑Cu in the surface water particulates is held in organic associations. When the material is deposited at the sediment surface, following its entry into the down-column carbon flux, the ∑Cu undergoes phase transformations as the organic carriers are destroyed. However, some of the organically associated copper (Cu₅) is preserved in the sediments, the amount depending on the diagenetic environment of deposition. The relationship between ∑Cu and organic carbon in an oceanic sediment may be masked, but the partitioning speciation data has shown that good correlations can be found between organic carbon and Cu₅. The concentration of Cu₅ in Atlantic Ocean surface sediments is highest in hemipelagic (diagenetically active) sediments deposited in the marginal regions, and lowest in open-ocean (less diagenetically active) sediments of the Mid-Atlantic Ridge and ridge flanks. The marginal sediments contain an average of 20% of their total Cu in an organic association, with the result that these sediments can act as traps for seawater-derived Cu that would normally be regarded as being ‘reactive’ in the marine environment. To a first approximation, the preservation of Cu₅ in the sediments mimics that of primary production in the overlying waters, and so ‘fingerprints’ the operation of the global ocean carbon flux in oceanic deposits. However, the relationship can be perturbed by the off-shelf transport of organic-rich, Cu₅-containing, turbidites which can result in the transfer and burial of organic copper host fractions in open-ocean oxic environments.     

Comparison of marine gas hydrates in sediments of an active and passive continental margin

Two sites of the Deep Sea Drilling Project in contrasting geologic settings provide a basis for comparison of the geochemical conditions associated with marine gas hydrates in continental margin sediments. Site 533 is located at 3191 m water depth on a spit-like extension of the continental rise on a passive margin in the Atlantic Ocean. Site 568, at 2031 m water depth, is in upper slope sediment of an active accretionary margin in the Pacific Ocean. Both sites are characterized by high rates of sedimentation, and the organic carbon contents of these sediments generally exceed 0.5%. Anomalous seismic reflections that transgress sedimentary structures and parallel the seafloor, suggested the presence of gas hydrates at both sites, and, during coring, small samples of gas hydrate were recovered at subbottom depths of 238m (Site 533) and 404 m (Site 568). The principal gaseous components of the gas hydrates wer methane, ethane, and CO₂. Residual methane in sediments at both sites usually exceeded 10 mll^?1 of wet sediment. Carbon isotopic compositions of methane, CO₂, and ΣCO₂ followed parallel trends with depth, suggesting that methane formed mainly as a result of biological reduction of oxidized carbon. Salinity of pore waters decreased with depth, a likely result of gas hydrate formation. These geochemical characteristics define some of the conditions associated with the occurrence of gas hydrates formed by in situ processes in continental margin sediments.