Carbon and nitrogen isotope excursions in mid-Pleistocene sapropels from the Tyrrhenian Basin: Evidence for climate-induced increases in microbial primary production

The modern Mediterranean Sea is oligotrophic, yet its sediment record contains layers of organic-carbon-rich sapropels at 21 ky (precessional) spacing that imply periods of elevated paleoproductivity that approached the high productivities of modern upwelling systems. Resolution to this paradox is provided by lines of evidence suggesting that the mode of primary productivity changed from one dominated by algae to one during times of sapropel deposition in which photosynthetic bacteria were important. We have made a high-resolution comparison of the organic carbon and nitrogen isotopic compositions of three sapropels and their background sediments in a 3-m sequence that corresponds to 1001 to 946 ka. Organic δ¹³C values systematically increase from − 26‰ to − 21‰ and δ¹⁵N values systematically decrease from 4‰ to < 0‰ as organic carbon mass accumulation rates increase in the sapropel layers. The increase in carbon isotope values mirrors the increases in primary productivity and associated organic matter export indicated by the increased mass accumulation rates. The decrease in nitrogen isotope values implies major contributions of nitrogen-fixing cyanobacteria to the total marine productivity. The precessional minima with which sapropels coincide were times of wetter climate that stratified the surface Mediterranean Sea, increased delivery of soil-derived phosphorus, and evidently amplified microbial primary production. Our high-resolution study reveals several relatively rapid excursions into and out of the high-productivity mode that suggest that sapropel deposition was a climate-sensitive surface-driven phenomenon that was not accompanied by basin-wide stagnation.     

Carbon isotopic composition and lattice-bound carbonate of Peru-Chile margin phosphorites

New light-stable carbonate-carbon isotope and lattice-bound CO₂ data from Quaternary Peru-Chile margin phosphatic nodules, crusts and pelletal grains, and from associated dolomicritic concretions, are presented, which provide constraints on the timing and mechanisms of growth of these phases in organic carbon-rich sediments. Comparison of δ¹³C values from carbonate fluorapatite (CFA) nodules and pelletal grains (−4.8 to 0.0‰ and −2.9 to +1.0‰ PDB, respectively) with pore-water total dissolved δ¹³C values from these sediments suggests early authigenic CFA precipitation from pore waters within a few centimeters of the sediment-water interface in association with suboxic to perhaps anoxic microbial degradation of organic matter. In contrast, the dolomicritic cores of nodules recovered from about 12°S display both strongly negative to positive δ¹³C values (−10.8 to +6.1‰) characteristic of formation deeper in the sediments in association with methanogenic and perhaps sulfate reduction microbial processes.

The amount of structural carbonate in CFA suggests that carbonate substitution generally increases as δ¹³C in CFA decreases, a probable consequence of increasing carbonate and accompanying charge-balancing substitutions in the CFA lattice in response to increasing pore-water carbonate ion concentrations with depth below the sediment-water interface. In one buried upward-growing nodule, decreasing CFA δ¹³C and increasing structural CO₂ also correspond to decreasing CFA growth rates. These data suggest that in addition to other constraints such as pore-water phosphorus and fluoride availability, the lower limit of CFA precipitation in suboxic to anoxic sediments may be controlled by lattice poisoning due to excessive dissolved carbonate ion concentrations. In organic-rich Peru-Chile margin sediments this depth threshold appears to be at approximately 5–10 cm below the sediment-water interface where maximum CFA CO₂ contents of about 6 Wt.% occur; in less organic-rich settings, greater depths of precipitation of CFA may be anticipated. Below this relatively shallow depth of CFA precipitation on the Peru shelf, high pore-water alkalinity and associated elevated total dissolved carbon and carbonate ion concentration apparently favor the precipitation of authigenic carbonates.     

Burial rates of organic matter along the eastern Canadian margin and stable isotope constraints on its origin and diagenetic evolution

Organic carbon (OC) and nitrogen (N) contents and δ¹³C and δ¹⁵N values in total organic matter (OM) were measured in sub-surface sediments (0–30 cm sub-bottom) from 21 cores raised from the Laurentian Channel of the Gulf of St. Lawrence and the Labrador Sea, to document OM fluxes and storage along the eastern Canadian margin. Storage rates as high as 2.5 g m⁻² yr⁻¹ for OC and 0.2 g m⁻² yr⁻¹ for N are observed in the Laurentian Channel, suggesting that the shelf plays a significant role in terms of OM storage (from 1 to 2% of the primary production). Based on the isotopic composition of the essentially marine OM of the Labrador Sea (δ¹³C/V-PDB=−21.9±0.4‰; δ¹⁵N/AIR=7.6±0.6‰; n=12), there is no isotopic evidence for a significant relative input of terrestrial OM along the Laurentian Channel (δ¹³C/V-PDB=−21.9±0.4‰; δ¹⁵N/AIR=8.0±0.9‰; n=10), either due to high relative fluxes of marine OM and/or to the trapping of continental OM in the estuary and upstream. High storage rates of OM are also observed on the continental rise of the Labrador Sea (as high as 1.1 g C m⁻² yr⁻¹ and 0.09 g N m⁻² yr⁻¹). They contrast with one order of magnitude lower rates on the slope, due to low sedimentation rates (SR) and sediment winnowing by the Western Boundary Undercurrent (WBUC). Reduced early diagenetic alteration of OM is observed, particularly in the Laurentian Channel. It results in discrete (i) losses of OC and N, (ii) shifts in C/N ratios, suggesting preferential removal of N-bearing OM also highlighted by losses in total hydrolysable amino acids (HAA). In the Labrador Sea slope records, due to low SR, OM concentration changes linked to long term temporal variations may superimpose on these diagenetic trends, and some influence of the WBUC is noticeable.     

中太平洋富钴结壳中生物标志物、有机碳同位素地球化学及其古海洋环境意义

利用2003年大洋DY105-12,14航次在中太平洋海山获取的KXD28富钴结壳样品,采用气相色谱(GC)内标法对该结壳样品的分层样进行了可溶有机质(氯仿沥青“A”)及其族组成(饱和烃、芳烃、非烃)、正构烷烃、类异戊二烯烃的定量分析,并结合总有机碳(TOC)及有机碳同位素(δ¹³C)分析,探讨了结壳样品有机质来源及富钴结壳组成与生长环境之间的关系。结果表明:(1)富钴结壳中有机质生物母源主要为海洋生物和菌藻类,并混有少量陆源物质;有机碳同位素同样也指示了海洋水生生物碳同位素特征;(2)KXD28结壳从底层到最外层有机碳同位素发生了很大变化,结壳中有机碳同位素组成变化与结壳生长过程中的海洋环境气候相符合:富钴结壳生长前期δ¹³C组成由正变负,对应全球气候变冷,南极底层流向太平洋挺进;而富钴结壳生长后期δ¹³C逐渐偏正,与全球气候变暖和南极底层流萎缩相关联。     

Nature and composition of shore-zone sediments between Jeddah and Yanbu, eastern Red Sea

The shore-zone sediments between Jeddah and Yanbu, west coast of Saudi Arabia, are composed mostly of skeletal carbonate sands. The nearshore sediments containing benthic foraminifera, algal fragments and molluscs are multimodal, the mean grain size varying between 0.76 and 2.35 ø. The beach sediments, except samples dominated by cerithid gastropods in some localities, are relatively finer than the nearshore sediments. Although the beaches to a great extent comprise sand-sized material, fine lime muds and coarse clastic gravels occur in certain areas. The dune sediments comprising mostly algal grains and ooids are very fine with 50 percent of the material in the 0.25–0.18 mm size grade. Except a general northward decrease in mean grain size, regional trends in the textural parameters of the sediments between Jeddah and Yanbu are not quite apparent. Lateral variations in the textural characteristics suggest a landward migration of the sediments in the shore zone under the influence of northerly and northwesterly winds. The carbon and oxygen (δ ¹³C + 4.80 to 4.84‰ PDB) (δ ¹³O − 0.04 to + 0.53‰ PDB) isotopic ratios of the lime muds occurring in certain shallow margins in the shore-zone, which are much higher than those of the green algae, indicate that the fine carbonates are at least in part inorganic in origin.

Like the shallow-water carbonates in tropical seas, aragonite and high Mg-calcite are the dominant carbonate minerals in the shore-zone sediments. There is a landward increase in aragonite contents caused by the landward migration of fine material from the nearshore. The dominant clay mineral in the nearshore sediments is kaolinite with subordinate swelling chlorite and little illite. Kaolinite is contributed by the coastal regions under the sub-tropical humid climate. Swelling chlorite is considered to have been formed in the nearshore by mechanical mixture of chlorite and montmorillonite derived from the metamorphic and igneous terrains of the Tertiary mountains bordering the coastal plain.     

Sediment dynamics in the Eurasian Arctic Ocean during the last deglaciation — The clay mineral group smectite perspective

This study focuses on sedimentological investigations of sediment cores recovered during the international Arctic′91, expeditions with the German research ice breaker RV “Polarstern” to the European sector of the Arctic Ocean. Here, we deduce the last glacial/interglacial changes in transport mechanism and sedimentation from the clay mineral group smectite. We choose the smectites as an example of how sediment mineralogy can be linked with particular source regions (the Kara and Laptev seas), distinct transport mechanism (sea ice and surface currents) and sedimentation processes. Smectite contents in Arctic sediments discussed for two time slices, including the Last Glacial Maximum (LGM), and the last deglaciation (Termination I), reveal the highest variability subsequent to the retreat of the Eurasian ice sheets. Our results show that smectite anomalies in the Eurasian Basin are associated with distinct meltwater pulses and occurred around 13.5–13.0 ¹⁴C ka B.P. Compelling evidence is provided that these anomalies are deduced from sea-ice entrained sediments from the eastern Kara Sea that entered the Arctic Ocean after ice-sheet break-up and eventually flooding of the Kara Sea. We propose that smectite anomalies in sediments of the eastern Arctic Ocean can be utilized to identify deglacial events and to help decipher configurations of the Eurasian ice sheets. The identification of smectite maxima along the modern sea-ice edge in the Eurasian Basin further indicates biologically enhanced sedimentation from melting sea ice allowing the reconstruction of seasonally open water in the region. Hence, considering the poor preservation conditions of primary paleoceanographic proxies in the Arctic Ocean, the clay mineral contents, particularly the smectite group, may be one alternative tool for paleoclimatic reconstruction in the Eurasian Basin.     

Stable isotope evidence for a marine origin of ophicalcites from the north-central Apennines (Italy)

Carbon and oxygen isotope ratios of 59 samples of Mesozoic ophicalcites from the north-central Apennines were measured. Strontium content and isotope ratios were only determined for selected samples.

The data obtained (−4.1 ≤ δ ¹³C ≤ + 3.0; 16.5 ≤ δ ¹⁸O ≤ 30.1; 0.7076 ≤ ⁸⁷Sr/⁸⁶Sr ≤ 0.7086; 60 ≤ Sr ppm ≤ 1140) suggest that the carbonate cement of the Apennines ophicalcites had a marine origin.

The ¹⁸O/¹⁶O values of most of the carbonates studied, however, indicate that the rocks have interacted with hydrothermal fluids, dominantly represented by sea water. In particular, the rocks from the northern section of the Apennines apparently reequilibrated their δ ¹⁸O content at higher temperature than those from the central zone.

Strontium isotope ratios, close to the Cretaceous—Cenozoic ocean water values, are well in agreement with such a kind of sea water/ophicalcites interaction, even if the carbonate cement formed earlier during the Jurassic period.     

海南儋州湾红树林区沉积有机质来源及碳储量

本文测定了海南儋州湾南岸柱状沉积物的粒度、总有机质参数(TOC、C/N和 δ13C)和类脂生物标志物含量,并通过端元混合模型使用红树植物特征标志物蒲公英萜醇含量、长链正构烷烃含量和δ13C值半定量区分了海南儋州湾南岸沉积有机质来源,尤其是红树林的贡献.另外,通过估算沉积物的有机碳储量来评估儋州湾红树林区域的储碳能力.在...     

Glacial deep-water properties in the west-equatorial Pacific: bathyal thermocline near a depth of 2000 m

The stable isotope stratigraphy of Planulina wüllerstorfi in three box cores from Ontong Java Plateau in the western equatorial Pacific shows that there existed a bathyal thermocline near the depth of 2000 m during glacial time. Waters below the boundary were colder by about 1°C, those above were about the same as now. The deep waters were slightly enriched and the upper waters depleted in nutrients, compared with present values. The differences in δ¹³C to the present (after correcting for the global change) are of the order of 0.1‰ more positive (above 2000 m) and 0.1‰ more negative (below), corresponding to changes in phosphate of the order of 0.1 μmol/kg (less phosphate above, and more below the boundary).     

Origin of sedimentary organic matter in the north-western Adriatic Sea

In order to evaluate the origin and the transformation of organic matter on the shallow shelf of the NW Adriatic Sea, organic carbon, total nitrogen and stable isotope ratios of organic carbon were analysed in riverine suspended matter and sediments as well as in marine suspended and sedimentary organic matter, in marine phytoplankton and zooplankton.The deposition of organic matter is influenced by fine sediment concentration. Surface sediments were characterised by highly variable biogeochemical conditions on the sea floor, whereas sub-surface sediments showed a more homogeneous hypoxic/anoxic environment.Low C_org/N ratio and high organic carbon and nitrogen concentrations in riverine suspended organic matter indicate an important contribution of freshwater phytoplankton within rivers, particularly during low flow regimes, which adds to the marine phyto- and zooplankton at shelf locations.In order to evaluate the importance of terrestrial, riverine and marine sources of OM in shelf sediments, a three end-member mixing model was applied to shelf surface sediments using ¹³C/¹²C values for organic matter and N/C ratios. The model showed an elevated contribution of terrestrial organic substances at intermediate depths (10–15 m), mostly corresponding to an area of coarser grain-size, whereas the riverine and marine organic fractions were mainly accumulating near the coast and offshore, respectively.     

Organic matter characterization in a tropical estuarine-mangrove ecosystem of India: Preliminary assessment by using stable isotopes and lignin phenols

In order to characterize the sources and fate of organic matter (OM) in the Pichavaram estuarine-mangrove ecosystem (east coast of India), stable isotope (δ¹³C and δ¹⁵N) ratios and molecular lignin analyses were conducted in plant litter, benthic algae, sediment, particulate matter and in a variety of benthic invertebrate species. The δ¹³C signature of plant litter ranges from −29.75‰ to −27.64‰ suggesting that mangrove trees follow the C₃ photosynthetic pathway. Sedimentary δ¹³C signature (−28.92‰ to −25.34‰) demonstrates the greater influence of plant litter organic matter on sedimentary organic matter. Suspended particulate organic pool was influenced by terrestrial source and also seems to be influenced by the marine phytoplankton. Enriched signature of δ¹⁵N in surface sediments (4.66–8.01‰; avg. 6.69‰) suggesting the influence of anthropogenic nitrogen from agricultural fields and human settlements. Spatial chemical variability in availability of nitrogen and plant associated microbial interactions demonstrate variability in δ¹⁵N signature in mangrove plant litter. Two (lower and higher) trophic levels of invertebrates were identified with and observed >4‰ gradient in δ¹³C signal between these two trophic groups. The observed δ¹³C values suggest that the lower level invertebrates feed on phytoplankton and higher level organisms have a mixed source of diet, phytoplankton, sediment and particulate organic matter. Lignin phenol analyses explain that the benthic surface layer was almost free of lignin. The ratio between syringyl phenols to vanillyl phenols (S/V) is 1.14–1.32 (avg. 1.23) and cinnamyl phenols to vanillyl phenols (C/V) is 0.17–0.31 (avg. 0.24), demonstrate non-woody angiosperm tissues was the major sources of lignin to this ecosystem, while aldehyde to acid ratios (Ad/Al) describe diagenetic nature of sediment and is moderately to less degraded. A two-end-member mixing model indicate that the terrigenous OM was dominant in the estuarine zones, while in the mangrove zone terrigenous supply accounts for 60% and marine input accounts for 40%.     

Uranium-series and AMS C studies of modern phosphatic pellets from Peru shelf muds

Recent sediments and separated phosphate pellets ( 125–500 μm in diameter) from the Peru shelf have been analyzed for uranium decay-series isotopes and ¹⁴C in order to determine age relationships and mineralization rates. Uranium-series ages of pellets separated from one box core are significantly higher than AMS radiocarbon ages determined for the same pellets. These differences appear to be a consequence of mixing of an older generation of pellets with ones which are more recently formed. Postdepositional adsorption of reactive elements such as thorium and protactinium onto pellet surfaces may also contribute to the observed discordancy with radiocarbon ages.

Sediment radiocarbon and ²¹⁰Pb sediment results, as well as some trends in the uranium-series data, suggest that high concentrations of phosphate pellets have accumulated in some Peru shelf sediments without extensive reworking. Individual pellets apparently form very quickly, on time scales of a few years. Estimated authigenic uptake rates of phosphorus into pellets ranges from 0.5 to 9.40 μmol-P cm^{− 2} yr^{− 1}, somewhat higher than rates measured for nodules from the same area. This is consistent with observations that pelletal morphologies predominate over nodular forms within ancient phosphorite deposits.     

Geochemical evidence for variations in delivery and deposition of sediment in Pleistocene light–dark color cycles under the Benguela Current Upwelling System

Distinctive light–dark color cycles in sediment beneath the Benguela Current Upwelling System indicate repetitive alternations in sediment delivery and deposition. Geochemical proxies for paleoproductivity and for depositional conditions were employed to investigate the paleoceanographic processes involved in creating these cycles in three mid-Pleistocene intervals from ODP Sites 1082 and 1084. Concentrations of total organic carbon (TOC) vary between 3.5 and 17.1%. Concentrations of CaCO₃ vary inversely to TOC and Al, which suggests that both carbonate dissolution and terrigenous dilution contribute to the light–dark cycles. Opal concentrations are independent of both TOC and CaCO₃, therefore eliminating diatom production and lateral transport of shelf material as causes of the light–dark cycles. δ¹³C_org and δ¹⁵N_tot values do not vary across light–dark sediment intervals, implying that the extent of relative nutrient utilization did not change. The stable δ¹⁵N_tot values represent a balanced change in nitrate supply and export production and therefore indicate that productivity was elevated during deposition of the TOC-rich layers. Parallel changes in concentrations of indicator trace elements and TOC imply that changes in organic matter delivery influenced geochemical processes on the seafloor by controlling consumption of pore water oxygen. Cu, Ni, and Zn are enriched in the darker sediment as a consequence of greater organic matter delivery. Redox-sensitive metals vary due to loss (Mn and Ba) or enrichment (Mo) under reducing conditions created by TOC oxidation. Organic matter delivery impacts subsequent geochemical changes such as carbonate dissolution, sulfate reduction and the concentration of metals. Thus, export production is considered ultimately responsible for the generation of the color cycles.     

象山港潮滩沉积物有机质分布特征及物源影响分析

潮滩是陆海交互影响的重要区域,在陆海物质交换的过程中扮演着重要的角色.象山港位于浙江宁波,是典型的半封闭式港湾,受人类活动影响显著.本文取其重要支港西沪港为研究区,自其潮上带至潮间带采集表层沉积样品,进行总有机碳(Total Organic Carbon,TOC)、总氮(Total Nitrogen,TN)和稳定碳同位...     

珠江口沉积物有机质特征、来源及其对碳存储的意义

河口沉积物作为承接陆海过程的重要载体, 是有机质赋存的主要形式之一。本文研究了珠江口沉积物总有机碳、总氮含量和沉积物可溶性有机物三维荧光特征, 以及其在口内区、混合区和口外区空间差异和影响因素, 并结合碳稳定同位素(δ¹³C)估算了珠江口各区域沉积物中不同来源有机质的贡献。结果显示: (1)沉积物总有机碳和总氮含量空间变化相似, 口内区和混合区域沉积有机质含量显著高于口外区; 主成分分析发现, 口内区沉积有机质含量主要受径流输入的影响, 口外区主要受Fe³⁺的影响; (2)MixSIAR稳定同位素混合模型结果显示, 口内区和混合区沉积有机质以陆源为主, 口外区则以海源为主; (3)珠江口沉积物新生有机质较多, 可快速被利用, 总体上不利于有机碳存储; 而陆源输入导致口内区和混合区沉积有机质腐殖化程度较高, 有机碳可存储性相对较高, 口外受海源有机质和铁氧化物—有机质复合体的影响, 有机碳可存储性相对较低。本研究可为深入认知河口区沉积有机质的生物地球化学过程及有机碳存储提供参考。     

Sulfur and iron speciation in surface sediments along the northwestern margin of the Black Sea

The speciation of sedimentary sulfur (pyrite, acid volatile sulfides (AVS), S⁰, H₂S, and sulfate) was analyzed in surface sediments recovered at different water depths from the northwestern margin of the Black Sea. Additionally, dissolved and dithionite-extractable iron were quantified, and the sulfur isotope ratios in pyrite were measured. Sulfur and iron cycling in surface sediments of the northwestern part of the Black Sea is largely influenced by (1) organic matter supply to the sediment, (2) availability of reactive iron compounds and (3) oxygen concentrations in the bottom waters. Biologically active, accumulating sediments just in front of the river deltas were characterized by high AVS contents and a fast depletion of sulfate concentration with depth, most likely due to high sulfate reduction rates (SRR). The δ³⁴S values of pyrite in these sediments were relatively heavy (−8‰ to −21‰ vs. V-CDT). On the central shelf, where benthic mineralization rates are lower, re-oxidation processes may become more important and result in pyrite extremely depleted in δ³⁴S (−39‰ to −46‰ vs. V-CDT). A high variability in δ³⁴S values of pyrite in sediments from the shelf-edge (−6‰ to −46‰ vs. V-CDT) reflects characteristic fluctuations in the oxygen concentrations of bottom waters or varying sediment accumulation rates. During periods of oxic conditions or low sediment accumulation rates, re-oxidation processes became important resulting in low AVS concentrations and light δ³⁴S values. Anoxic conditions in the bottom waters overlying shelf-edge sediments or periods of high accumulation rates are reflected in enhanced AVS contents and heavier sulfur isotope values. The sulfur and iron contents and the light and uniform pyrite isotopic composition (−37‰ to −39‰ vs. V-CDT) of sediments in the permanently anoxic deep sea (1494 m water depth) reflect the formation of pyrite in the upper part of the sulfidic water column and the anoxic surface sediment. The present study demonstrates that pyrite, which is extremely depleted in ³⁴S, can be found in the Black Sea surface sediments that are positioned both above and below the chemocline, despite differences in biogeochemical and microbial controlling factors.     

Hardground formation in the Bannock Basin, Eastern Mediterranean

Twenty kilogrammes of crusts and slabs of indurated carbonate sediment, usually referred to as hardgrounds, were dredged along the eastern steep wall of the Bannock Basin during the 1984 cruise of R.V. Bannock.

The crusts range in thickness from one to a few centimetres and the fragments of these crusts are irregular in shape. Their surface is always uneven and their colour ranges from white to brownish dark grey. Some slabs are impregnated along one side by ferromanganese sesquioxides, and borings occur in several samples. Serpulid tubes have been observed in one instance. The borings and serpulids suggest formation of the hardgrounds at or close to the sediment/water interface and exposure at the seafloor.

The degree of lithification is generally different on the inferred upper and lower sides of the slabs. An upward increase of lithification across the slabs is reflected by mineralogy, ultrastructure and stable isotope composition of the carbonate. X-ray diffraction analyses indicate high-magnesian calcite as the predominant carbonate with minor amounts of low-magnesian calcite and dolomite. Occasionally, large gypsum crystals are attached to the hardgrounds and sometimes smaller ones are dispersed through the carbonate matrix.

An increase in diagenesis is reflected by the passage from friable, nodular nannofossil chalk to nannofossil limestone and hard xenotopic calcite micrite. Overgrowth of coccoliths and internal cementation of the tests of planktonic foraminifera by high-Mg calcite increase from chalk to limestone. In the hard, fully cemented micrites, coccoliths can no longer be recognised in the xenotopic fabric. Pteropods occur as dissolution moulds with aragonite preserved as only tiny relics.

Carbon and oxygen isotope analyses were performed on different samples. The progressive lithification to chalk and limestone is marked by a shift in the δ¹⁸O values from +1.2‰ to +5.4‰ (PDB). This change indicates that precipitation of high-Mg calcite and possibly also recrystallisation of the original biogenic carbonate took place within cold and hypersaline brines which were enriched in ¹⁸O. The oxygen isotope data suggest that lithification and gypsum precipitation occurred under identical conditions. The carbon isotope data show progressive diagenetic change from values near +1‰ to values of +3‰. This change may reflect a contribution of methanogenetic CO₂ to the hypersaline brine.     

A contemporary sediment and organic carbon budget for the Kara Sea shelf (Siberia)

It has recently been realized that the Arctic undergoes drastic changes, probably resulting from global change induced processes. This acts on the cycling of matter and on biogenic elements in the Arctic Ocean having feedback mechanisms with the global climate, for example by interacting with atmospheric trace gas concentration. A contemporary budget for biogenic elements as well as suspended matter for the Arctic Ocean as a baseline for comparison with effects of further global change is, thus, needed. Available budgets are based on the late Holocene sedimentary record and are therefore quiet different from the present which has already been affected by the intense anthropogenic activity of the last centuries.

We calculated a contemporary suspended matter and organic carbon budget for the Kara Sea utilizing the numerous available data from the recent literature as well as our own data from Russian-German SIRRO (Siberian River Run-off) expeditions. For calculation of the budgets we used a multi-box model to simplify the Kara Sea shelf and estuary system: input was assumed to comprise riverine and eolian input as well as coastal erosion, output was assumed to consist of sedimentation and export to the Arctic Ocean. Exchange with the adjacent seas was considered in our budget, and primary production as well as recycling of organic material was taken into account. According to our calculations, about 18.5 × 10⁶ t yr^− 1 of sediments and 0.37 × 10⁶ t yr^− 1 of organic carbon are buried in the estuaries, whereas 20.9 × 10⁶ t yr^− 1 sediment and 0.31 × 10⁶ t yr^− 1 organic carbon are buried on the shelf. Most sources and sinks of our organic carbon budget of the Kara Sea are in the same order of magnitude, making it a region very sensitive to further changes.     

Late Quaternary carbonate sedimentation at the Sierra Leone Rise (eastern equatorial Atlantic Ocean)

In the eastern equatorial Atlantic Ocean, changes in the concentration of carbonate in Late Quaternary sediments resulted from reduced production of carbonate in surface waters and increased dilution with non-carbonate sediments during glacial maxima. During glacial stages, production of carbonate in surface water (measured as its accumulation rate in shallow, undissolved cores) decreased by one half. The glacial accumulation rate of non-carbonate components increased 1.5 to 4 times over Holocene values; the greatest increases occurred in the deepest cores.

Carbonate dissolution during stages 2, 3 and 4 increased the proportion of foraminiferal fragments and decreased the accumulation rate of susceptible species in the deep sites. In shallow sites, slightly increased dissolution can be detected during stage 3 while greatly increased dissolution occurred during stage 4. Bathymetric profiles of foraminiferal fragmentation and accumulation document a shoaling of the foraminiferal lysocline by 1000 m during glacial isotopic stages. We present a mass balance model of sediment accumulation for carbonate and insoluble components and from this model we estimate the rate of downslope transport and dissolution of carbonate at the Sierra Leone Rise. Our results show that during stage 4 the rate of carbonate loss to dissolution was greater than the rate observed today or during other interglacial stages. The calculated rates of dissolution for stages 2 and 3 are not significantly different from those calculated for stage 1.     

西太平洋马尔库斯-威克海山区沉积物中生物硅含量分布

分析了大洋40航次在西太平洋马尔库斯-威克海山区山间海盆采集的表层沉积物中生物硅和有机质的含量,并对其分布特征和来源进行了初步的研究。结果表明,马尔库斯-威克海山区附近海域深海表层沉积物中生物硅含量总体较低,含量在0.88%～12.41%之间,平均含量为2.19%,分布上呈现西南含量高,向东北方向递减的趋势;深海表层沉积物中有机碳含量较低,δ¹³C同位素组成分布与生物硅相同。沉积物柱状样的研究表明研究区在过去的100～200 ka期间表层水体中硅质生物的初级生产力是逐渐增加的。