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1.
According to bioassay studies and high dissolved nutrient N/P ratios in the seawater column, phosphorus (P) is thought to control marine productivity in the northern Adriatic Sea. P in near-shore marine sediments of the Gulf of Trieste, the northernmost part of the Adriatic Sea, was investigated using pore water P distributions, and benthic P flux studies under oxic and anoxic conditions. The data show that P regeneration is up to three-fold more extensive in sediments overlain by oxygen-depleted waters and proceeds in parallel with Fe and Mn enhanced benthic fluxes. It appears from the incubation experiments that degradation of sedimentary organic matter is the main contribution to the flux of P at the sediment–water interface, while the release of phosphate adsorbed on the iron oxide surface is of minor importance.It appears that about 50% of P in the Gulf of Trieste is retained within in the sediments, probably bonded to clay minerals and carbonate grains or precipitated as fluoroapatite. In these sediments total P (Ptot) is preserved preferentially over organic C (Corg). P regenerated from surficial sediments contributes about 1/3 of the P that is assimilated by benthic microalgae. The phytoplankton P requirement should be entirely supplied from fresh-water sources. These results suggest that oxygen depletion in coastal areas caused by eutrophication enhances P regeneration from sediments, providing the additional P necessary for increased biological productivity. The development of anoxic bottom waters in coastal areas enhances the recycling of P, exacerbating the nutrient requirement in the area. A geochemical record of P burial in a longer sedimentary sequence revealed an increasing trend of Ptot and organic P (Porg) contents occurring approximately 50 years BP (after 1950), probably due to increasing use of inorganic fertilizers and detergents in the area.  相似文献   

2.
Anoxic sulfidic waters provide important media for studying the effect of reducing conditions on the cycling of trace metals. In 1987–1988, dissolved and particulate trace metal (Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb) concentrations were determined in the water column of the anoxic Drammensfjord basins, southeastern Norway. The iminodiacetic acid type chelating resin (Chelex 100) was used for the preconcentration of trace metals. The trace metal concentrations were determined using atomic absorption spectrophotometry (AAS), differential pulse polarography (DPP), and differential pulse-anodic stripping voltammetry (DP-ASV).It was observed that the trace metals Mn and Fe were actively involved in the processes of redox cycling (oxidationreduction and precipitation-dissolution) at the O2/H2S interface. The dissolved concentrations of Mn, Fe and Co showed maxima just below the O2/H2S interface. The seasonal enhancement in the maxima of both dissolved and particulate Mn and Fe at the redox cline is mainly governed by the downward movement of water which carries oxygen. An association of Co with the Mn cycle was observed, while the total dissolved Ni was decreased by only 10–35% in the anoxic waters. The dissolved concentrations of Cu, Zn, Pb and, to a lesser extent, Cd decreased in the anoxic zone.  相似文献   

3.
In the anoxic hypersaline Tyro and Bannock Basins of the eastern Mediterranean, extremely high concentrations of Co (0.015%), Cu (1.35%) and Zn (0.28%) were found in suspended matter collected at the sharp interface between seawater and the anoxic brine. The high particulate Co, Cu and Zn concentrations can be explained by the sharp increase in dissolved sulphide at these interfaces, and the resultant precipitation of metal sulphides. The particulate As, Sb and Mo concentrations also showed a sharp maximum at or close to the interface. However, the contributions of As, Sb and Mo contents in suspended matter to the total concentrations in the water column are small. Scanning electron microscopy-energy-dispersive X-ray analysis (SEM-EDAX) of suspended particulate matter from the Tyro Basin revealed spherical particles strongly enriched in Fe, Cu and Zn at the seawater-brine interface.  相似文献   

4.
Iron-rich concretions are frequently found around plant roots in Tagus estuary (Portugal) where radial delivery of O2 takes place. Salt marsh sediments exhibit cracks that are an additional feature to introduce O2 and other solutes in the upper sediments. Metal concentrations in salt marsh sediments are clearly above the background levels reflecting the anthropogenic sources from a large city with 2.5 million inhabitants, and several industrial centres. In order to evaluate how both oxidised structures influences the redistribution of redox sensitive elements in salt marsh sediments, concretions were collected from roots of Halimione portucaloides below the oxygenated zone. These tubular cylindrical structures were analysed for Fe, Al, Mn, As, and P along 1-cm radial transect in a millimetre scale from the inner part to the adjacent anoxic sediment. In addition, oxidised cracks were analysed for the same spatial resolution, from the sediment–water interface to anoxic layers (2-cm transept). The parallelism between Fe, As, and P concentrations at this microscale is the most noticeable aspect. Iron and As presented very high concentrations in the 4-mm concretions (3.4 mmol g−1 and 3.1 μmol g−1, respectively) and decreased sharply to the host sediment. Oxygen released from roots oxidise the solid sulphides, and the reduced Fe and As are transported towards the root by both diffusion and pore water flow associated with the root water uptake. Subsequently, Fe(III) precipitates and As is retained by sorption and/or coprecipitation. These elements are also enriched in the first 2-mm of oxidised cracks, but in lower concentrations (50% and 30%, respectively). Manganese concentrations in concretions were low (11.8 μmol g−1), indicating that Fe dominates the sediment chemistry. Phosphorus and iron concentrations in the ascorbate fraction were higher in the oxidising surfaces of concretions (10.7 μmol g−1 and 1.6 mmol g−1, respectively) and of cracks (5.1 μmol g−1 and 0.47 mmol g−1). The parallelism of Fe and As distributions includes not only their similar redox chemistries, but also that to phosphate, including control by coprecipitation of the host iron phases. The mechanisms involved in the mobilisation of As and P are however different, whereas As comes from the oxidation of iron sulphides; dissolved P derives from reduction of ferri-hydroxide phases.  相似文献   

5.
The uppermost 5–6 cm of the sediments (between 8 and 2248 m water depths) were studied to understand the effects of varying redox conditions on the Mn distribution in the recent sediments of the Black Sea. It was found that most Mn concentrations are consistent with the average abundance in crustal and/or sedimentary rocks. There exist no important differences between Mn concentrations in oxic (shallower water; <70 m) and anoxic (deeper water; 120 m) sediments. Previously reported Mn-enrichment above the Black Sea oxic/anoxic interface, due to the peculiar redox cycling, shows no significant contribution of Mn to the bottom sediments. A marked relationship between total Mn concentrations and clay/mud contents at shelf depth along the southern Black Sea margin indicates increased accumulation of Mn in association with the fine-grained particles and eastward water circulation.  相似文献   

6.
Framvaren, a super-anoxic fjord in southern Norway, contains 7–8 mmoll−1 of sulphide and a total carbonate concentration of 18.5 mmol kg−1 in the bottom water. The chemistry of calcium has been studied, considering sources, biogenic and chemical processes and sedimentary sinks. Calcium associated with the bacteria biomass at the redox interface (18m depth) appears to be the primary source of dissolved calcium in the deep, anoxic water. Excess calcium and high total carbonate cause supersaturation of calcite, which is precipitated chemogenically. Calcite (and presumably some aragonite) is identified both in sediment trap material and the bottom sediments below the depth of supersaturation.  相似文献   

7.
N2O Production, Nitrification and Denitrification in an Estuarine Sediment   总被引：1，自引：0，他引：1  
The mechanisms regulating N2O production in an estuarine sediment (Tama Estuary, Japan) were studied by comparing the change in N2O production with those in nitrification and denitrification using an experimental continuous-flow sediment–water system with15N tracer (15N-NO−3 addition). From Feburary to May, both nitrification and denitrification in the sediment increased (246 to 716 μmol N m−2 h−1and 214 to 1260 μmol N m−2 h−1, respectively), while benthic N2O evolution decreased slightly (1560 to 1250 nmol N m−2 h−1). Apparent diffusion coefficients of inorganic nitrogen compounds and O2at the sediment–water interface, calculated from the respective concentration gradients and benthic fluxes, were close to the molecular diffusion coefficients (0·68–2·0 times) in February. However, they increased to 8·8–52 times in May except for that of NO−2, suggesting that the enhanced NO−3 and O2supply from the overlying water by benthic irrigation likely stimulated nitrification and denitrification. Since the progress of anoxic condition by the rise of temperature from February to May (9 to 16 °C) presumably accelerated N2O production through nitrification, the observed decrease in sedimentary N2O production seems to be attributed to the decrease in N2O production/occurrence of its consumption by denitrification. In addition to the activities of both nitrification and denitrification, the change in N2O metabolism during denitrification by the balance between total demand of the electron acceptor and supply of NO−3+NO−2 can be an important factor regulating N2O production in nearshore sediments.  相似文献   

8.
The Thau Lagoon, a French Mediterranean shallow lagoon, is a site where extensive shellfish farming occurs. The aim of the present work is to evaluate the role of this activity on nutrient exchange at the sediment-water interface in relation to organic matter (OM) sedimentation and degradation. Two stations inside (C5) and outside (C4) of the shellfish farming areas were sampled at three seasons. Porewater chemistry surveys and calculated diffusive fluxes were used to evaluate the trophic status of the Thau lagoon. Quantitative (Particulate Organic Carbon) as well as qualitative OM (Hydrogen Index, Carbohydrates) analyses were performed on sediments to assess OM characteristics. Results emphasized that surficial sediments at C5 are always more enriched in OM. Porewater nutrient concentrations are 10-20 times higher at C5 than at C4. In June 2003, the porewater profiles exhibit a sharp gradient at the bottom waters, indicating a hypereutrophic status, leading to an anoxic crisis.  相似文献   

9.
Vertical distributions of dissolved species across the sediment–water interface (SWI), including major cations (sodium, potassium, magnesium, calcium), minor cations (lithium, strontium, barium), redox sensitive species (dissolved manganese, iron, sulfate, sulfide, ammonium) and other chemical parameters (pH, alkalinity, soluble reactive phosphorous, dissolved silica) were studied in a Mediterranean lagoon used for intensive shellfish farming. In order to quantify the impact of this activity on diagenetic processes and the influence of seasonal changes, two stations contrasted with respect to organic carbon fluxes were sampled in Thau lagoon from March 2001 to August 2002 during four field campaigns in winter, spring, summer and fall. Well-defined layers enriched with redox sensitive species were observed following the conventional sequence of early diagenetic reactions. However, differences were observed between both stations in depths and thickness layers. Concentration gradients extended down to more than 92 cm depth at the central position of the lagoon (station C4 – 8 m depth) and down to 40 cm depth inside shellfish farming zones (station C5 – 9 m depth). Station C4 showed an unusual diagenetic signature: sharp dissolved oxygen, iron, nitrate and manganese gradients existed at the SWI but gradients of dissolved sulfide and alkalinity as well as other parameters (dissolved silica, Ba, etc.) were recorded only from 25 to 30 cm depth downward. Seasonal changes were observed in pore water composition as deep as 30–50 cm in station C4 (only 15 cm in station C5). The center of the lagoon is not directly subjected to biodeposits deriving from shellfish activity. Isotopic and bioturbation data allowed to rule out a reworking of the sediment deeper than a few centimeters. In addition to organic content of the sediment, physical parameters were likely to induce the 10–20 cm gap between dissolved iron and sulfide profile as well as the higher vertical extent of diagenetic sequence observed at station C4. Conversely to station C5, station C4 underwent stronger currents and wave effect probably generating advective transport of water through the sediment, but no permeability data were available to confirm this hypothesis. During summer, climatic conditions generated vertical stratification of the water column and transient suboxic conditions at the bottom. Such conditions drove the upward shift of redox fronts, compacting the diagenetic sequence. These effects were reinforced at station C5 by shellfish and its farm structures (mainly attenuation of current and increased heat absorption).  相似文献   

10.
The Arcachon lagoon is a 156 km2 temperate mesotidal lagoon dominated by tidal flats (66% of the surface area). The methane (CH4) sources, sinks and fluxes were estimated from water and pore water concentrations, from chamber flux measurements at the sediment–air (low tide), sediment–water and water–air (high tide) interfaces, and from potential oxidation and production rate measurements in sediments. CH4 concentrations in waters were maximal (500–1000 nmol l−1) in river waters and in tidal creeks at low tide, and minimal in the lagoon at high tide (<50 nmol l−1). The major CH4 sources are continental waters and the tidal pumping of sediment pore waters at low tide. Methanogenesis occurred in the tidal flat sediments, in which pore water concentrations were relatively high (2.5–8.0 μmol l−1). Nevertheless, the sediment was a minor CH4 source for the water column and the atmosphere because of a high degree of anaerobic and aerobic CH4 oxidation in sediments. Atmospheric CH4 fluxes at high and low tide were low compared to freshwater wetlands. Temperate tidal lagoons appear to be very minor contributor of CH4 to global atmosphere and to open ocean.  相似文献   

11.
In the estuary of the river Scheldt, where an oxygen gradient exists in addition to the salinity gradient, redox processes will be of major importance for trace metal mobilisation. In this study, the influence of salinity and pH on the redox processes of dissolved Zn and Cd sulphides is investigated together with the effects on the ratio of the dissolved Zn and Cd concentrations. The speciation of these metals is calculated with the chemical equilibrium programme +. Zn sulphides are oxidised at lower oxygen concentrations than Cd sulphides, due to lower stability constants, causing a sudden increase or peak in the dissolved Zn/Cd ratio. The formation of dissolved Cd chloride complexes when oxidation occurs at high salinities (S=15) increases the mobility of Cd, causing a decrease in the Zn/Cd peak of the total dissolved concentrations. The peak is three to four times smaller at S=15 than when oxidation occurs at S=2. The simple model calculations compare very well with field data. The Scheldt estuary is suitable to illustrate these calculations. In the 1970s, the anoxic part of the estuary reached S=15–20, but since the early 1980s it has dropped to S=2–10. Historic data on metals in the estuary from 1978, 1987 and the 1990s were used to compare with the equilibrium calculations. The increase of the dissolved Zn/Cd peak at low salinity as a consequence, of the decreasing anoxic region is confirmed well by the data. The good agreement between model calculations and field data is a proof of the extreme importance of redox processes for the solubility of Zn and Cd sulphides in the estuary.  相似文献   

12.
Depth profiles of the naturally-occurring radionuclides 238U, 234U, 226Ra, 228Ra and 228Th were obtained in two diverse anoxic marine environments; the permanently anoxic Framvaren Fjord in southern Norway and the intermittently anoxic Saanich Inlet in British Columbia. Concentrations of total H2S were over three orders of magnitude greater in the anoxic bottom waters of Framvaren Fjord compared to those in Saanich Inlet.In Framvaren Fjord, the O2/H2S interface was located at 17 m. While dissolved 238U behaved conservatively throughout the oxic and anoxic water columns, concentrations based on the 238U/salinity ratio in oxic oceanic waters were almost 30% lower. Dissolved 226Ra displayed a sharp maximum just below the O2/H2S interface, coinciding with dissolved Mn (II) and Fe (II) maxima in this zone. It is suggested that reductive dissolution of Fe-Mn oxyhydroxides remobilizes 226Ra in this region.In Saanich Inlet, the O2/H2S interface was located at 175 m. Dissolved 238U displayed a strongly nonconservative distribution. The depth profiles of dissolved 226Ra and 228Th correlated well with the distribution of dissolved Mn (II) in the suboxic waters above the O2/H2S interface, suggesting that reduction of particulate Mn regulates the behavior of 226Ra and 228Th in this region.Removal residence times for dissolved 228Th in the surface oxic waters of both systems are longer than those generally reported for particle-reactive radionuclides in coastal marine environments. In the anoxic waters of Framvaren Fjord and Saanich Inlet, however, the dissolved 228Th removal residence times are quite similar to values reported for dissolved 210Pb in the anoxic waters of the Cariaco Trench and the Orca Basin. This implies that the geochemistries of Th and Pb may be similar in anoxic marine waters.  相似文献   

13.
Geochemical and rock-magnetic investigations were carried out on a sediment core collected from the SE Arabian Sea at 1420 m depth in oxygenated waters below the present-day oxygen minimum zone. The top 250 cm of the core sediments represent the last 35 kaBP. The · 18O values of Globigerinoides ruber are heaviest during the Last Glacial Maximum (LGM) and appear unaffected by low-saline waters transported from the Bay of Bengal by the strong northeast monsoon and West Indian coastal current. The signatures of Bølling-Allerød and Younger Dryas events are distinct in the records of magnetic susceptibility, organic carbon (OC) and · 18O. Glacial sediments show higher OC, CaCO3, Ba, Mo, U and Cd, while the early-to-late Holocene sediments show increasing concentrations of OC, CaCO3, Ba, Cu, Ni and Zn and decreasing concentrations of Mo, U and Cd. Productivity induced low-oxygenated bottom waters and reducing sedimentary conditions during glaciation, and productivity and oxygenated bottom waters in the Holocene are responsible for their variation. The core exhibits different stages of diagenesis at different sediment intervals. The occurrence of fine-grained, low-coercivity, ferrimagnetic mineral during glacial periods is indicative of its formation in organic-rich, anoxic sediments, which may be analogous to the diagenetic magnetic enhancement known in sapropels of the Mediterranean Sea and Japan Sea. The glacial sediments exhibiting reductive diagenesis with anoxic sedimentary environment in this core correspond to reductive diagenesis and intermittent bioturbation (oxygenation) reported in another core in the vicinity. This suggests that the poorly oxygenated bottom water conditions during glacial times should not be generalized, but are influenced locally by productivity, sedimentation rates and sediment reworking.  相似文献   

14.
A mass balance of the naturally occurring short-lived radium isotopes (223,224Ra) in the Venice Lagoon was conducted by an integrated approach combining the directly estimated individual Ra contributions and hydrodynamic model results. Hydrodynamic data allows for the calculation of the Ra mass balance in sub-sections of the Venice Lagoon (boxes), which are characterized by physically homogeneous properties, instead of investigating the entire lagoon. Utilizing this method, both the seasonal and the spatial variability of the submarine groundwater discharge in the Venice Lagoon have been estimated. Between 14–83 × 109 L d− 1 of water were calculated to flow across the sediment–sea interface, corresponding to 5–28 times the mean annual river input. The submarine groundwater discharge estimates were correlated with the residence time calculation to better understand spatial and seasonal variation.  相似文献   

15.
Results of the chemical investigation on the Bannock and Tyro Basins are reported.Both basins were found to be hypersaline ( 10 times higher than salinity of normal seawater) and anoxic. In all investigated basins a region of transition, a few meters thick, was identified at depths > 3327 dbar. It is characterized by a sharp gradient of salinity, and all concentrations of analysed species increase strongly except for dissolved oxygen and nitrate, which immediately drop to zero. This region appears as a sharp boundary that prevents mixing. As a result, in the presence of organic matter, an anoxic condition developed with the complete depletion of dissolved oxygen. At the same time, hydrogen sulphide and ammonium accumulated within the brine. Between the Bannock and the Tyro brines differences occur in the measured concentrations of H2S, SO2−4, Ca2+ and NH3. There are some differences also within the Bannock area sub-basins.The Libeccio sub-basin, in the Bannock area, contains a double-layered brine: the upper layer is 140 dbar thick and the lower layer is 300 dbar thick. A second interface between upper and lower brines develops at a depth of 3500 dbar. Nearly all of the measured concentrations vs. depth show the double layer, with the exception of ammonium, the concentration of which remains nearly constant throughout the anoxic column. Profiles of the other species analyzed show remarkable differences on passing from the upper to the lower brine. Hydrogen sulphide, sulphate and fluoride concentrations appear constant and then increase at the second interface. The calcium concentration is also constant in the upper brine, but decreases at the second interface. Total alkalinity and phosphate concentrations show a maximum peak just below the first interface. However, after passing through the second interface all the chemical parameters exhibit an almost constant behaviour down to the bottom.Hypersaline conditions are attributed to the dissolution of Messinian evaporite, and anoxia is suggested to originate from the oxidation of organic matter present in sediments and from the absence of bottom water circulation in such a deep and enclosed environment.The chemical conditions can be summarized as follows: in the Libeccio Basin the values for the species analysed have the ranges: 39–321 psu for ‘salinity’, 8.2−6.5 for pH, 2.7–4.0 mM for total alkalinity, 0.2-0 mM for dissolved oxygen, 0–1669 μM for hydrogen sulphide, 0–198 μM for thiol, 31–99 mM for sulphate, 11–21 mM for calcium, 7–100 μM for fluoride, 0.2–3080 μM for ammonium, 5.8-0 μM for nitrite, 0.2–12 μM for phosphate and 8–130 μM for silicate.  相似文献   

16.
The metabolic inhibitor cycloheximide was used to estimate the influence of primarily unicellular eukaryotes (heterotrophic protozoa) on nutrient recycling in different types of sediments in the North Sea. Fluxes of dissolved inorganic nitrogen across the sediment–water interface were measured in undisturbed sediment cores (controls) and compared to fluxes in sediment cores with cycloheximide added. If eukaryotes play an important role in nutrient recycling, one would expect to find lower nitrogen sediment–water effluxes in cores with cycloheximide due to the inactivation of eukaryotes. This important role hypothesised for eukaryotes was not generally observed: Only at four of the nineteen stations were ammonium effluxes significantly higher in controls than in cores with cycloheximide, and at five stations nitrate effluxes were significantly higher in the controls than in the cores with cycloheximide. Eukaryotic activity apparently contributed to the sediment–water exchange of ammonium through mineralisation of organic matter, nitrification and the subsequent release of ammonium and nitrate at these stations. At most other stations no differences were obtained between controls and cores with cycloheximide. This suggests that bacteria were the most important nutrient mineralisers at these stations at the time of the cruises.  相似文献   

17.
A combination of CTD casts, discrete bottle sampling and in situ voltammetric microelectrode profiling was used to examine changing redox conditions in the water column at a single station south of the Bay Bridge in the upper Chesapeake Bay in late July/early August, 2002–2005. Short-term (2–4 h) fluctuations in the oxic/suboxic/anoxic interface were documented using in situ voltammetric solid-state electrodes. Profiles of dissolved oxygen and sulfide revealed tidally-driven vertical fluctuations of several meters in the depth and thickness of the suboxic zone. Bottom water concentrations of sulfide, Mn2+ and Fe2+ also varied over the tidal cycle by approximately an order of magnitude. These data indicate that redox species concentrations at this site varied more due to physical processes than biogeochemical processes. Based on analysis of ADCP data, tidal currents at this station were strongly polarized, with the principal axis of tidal currents aligned with the mainstem channel. Together with the chemical data, the ADCP analysis suggests tidal flushing of anoxic bottom waters with suboxic water from north of the site. The present study is thus unique because while most previous studies have focused on processes across relatively stable redox interfaces, our data clearly demonstrate the influence of rapidly changing physical mixing processes on water column redox chemistry.Also noted during the study were interannual differences in maximum bottom water concentrations of sulfide, Mn2+ and Fe2+. In 2003, for example, heavy spring rains resulted in severe hypoxia/anoxia in June and early July. While reported storm-induced mixing in late July/early August 2003 partially alleviated the low-oxygen conditions, bottom water concentrations of sulfide, Mn2+ and Fe2+ were still much higher than in the previous year. The latter implies that the response time of the microbial community inhabiting the suboxic/anoxic bottom waters to changing redox conditions is slow compared to the time scale of episodic mixing events. Bottom water concentrations of the redox-sensitive chemical species should thus be useful as a tracer to infer prior hypoxic/anoxic conditions not apparent from ambient oxygen levels at the time of sampling.  相似文献   

18.
氧化还原敏感元素(Redox Sensitive Elements,RSE)如V、Cr、Mo、U等,通常在氧化条件下呈溶解态,在还原沉积环境中除Fe、Mn外,RSE被还原成低价态转移至沉积物中富集积累,因此可以利用氧化还原敏感元素在沉积物中的富集情况反演沉积环境的氧化还原状况。本文通过研究东海内陆架季节性低氧海区Zb7沉积柱中氧化还原敏感元素V、Cr、Ni、Cu、Zn、Mo、U的垂直分布、富集特征和比值,探究沉积环境氧化还原状况;发现RSE/Al和富集系数自1978年以来呈增加的趋势,但自2009年开始有所降低,整体RSE富集系数均小于3,未见明显富集。RSE比值V/Cr<2、Ni/Co<5、U/Th<0.75、0.25<(Cu+Mo)/Zn<0.55,以及MoEF/UEF比值主要分布在0.08～0.3倍海水Mo/U值之间,均指示氧化的沉积环境。RSE/Al与Fe/Al、Mn/Al具有显著的相关性,表明RSE在剔除陆源碎屑输入后,主要通过与Fe、Mn氧化物结合进入沉积物,也指示氧化的沉积环境。研究结果与该区域溶解氧历史数据反映的季节性低氧结果不一致,可能与RSE在夏季季节性低氧时,沉积物中的富集信号在秋冬季溶氧水平恢复后缺失有关。尽管RSE不能有效指示东海季节性低氧环境,但Zb7沉积柱RSE在1978年后富集程度的增加以及2011年后的降低,在一定程度上反映了该区域自1978年后季节性低氧程度加重,2009年后又有所缓解的变化趋势。  相似文献   

19.
Concentrations of Se in the pore-water and in the solid phase, and the concentrations of other diagenetic constituents (Fe, Mn, phosphate, ammonium and I) in pore-water, were determined in a sediment core from a 350-m deep station in the lower St. Lawrence Estuary. The concentration of dissolved Se in pore-water was 2.1 nmol kg−1 at the surface of the core, increasing to a maximum of 7.6 nmol kg−1 at a depth of 12 cm, and thereafter decreasing gradually with depth. This profile is similar to the profiles of Fe and phosphate, whose concentration maxima occur around 10 cm. The concentration of total sedimentary Se remained almost constant with depth (≈ 0.75 mg kg−1); however, a significant enrichment of oxalate-leachable Se was observed in the top 2 cm. The sedimentary cycling of Se appears to be closely related to that of Fe: adsorption of Se onto Fe oxyhydroxide at or near the sediment-water interface, release of the adsorbed Se by the reduction of Fe oxyhydroxide, and removal by formation of ferroselite (FeSe2) at depth. The pore-water flux of Se was estimated by two different methods, firstly from the pore-water gradient, and secondly by applying a box model to the oxalate-leachable solid-phase Se data. The methods agree well both giving values for the flux of 0.11 nmol cm−2 year−1. This agreement suggests that the loss of labile Se in the sediment is balanced by the upward flux of dissolved Se.  相似文献   

20.
We investigated the composition, recycling, and mass accumulation rates of sediments along a transect in the Southern Ocean located from 66°S to 57°S at 170°W. This transect also corresponds to the location of a sediment trap mooring line. The sediments at the seven sites studied range from largely terrigenous material to nearly pure (>90%) biogenic silica. CaCO3 is a minor but persistent component at most sites. Mass accumulation rates have been determined on the basis of excess 230Th in the sediments, i.e., 230Th-normalized accumulation rates. The influence of redistribution of sediments on the sea floor has been estimated from 14C analyses. The recycling of material delivered to the sediments has been characterized on the basis of pore water studies that make extensive use of both in situ sampling and shipboard extractions. The influence of the highly variable rates of input of particulate matter that characterize much of the Southern Ocean upon pore water gradients and fluxes across the sediment water interface has been considered.We find only poor correspondence between BSiO2 burial fraction (=burial/particulate flux), a quantifiable measure of preservation efficiency, and BSiO2 particulate rain along the transect. However, preservation does appear to be closely linked to a combination of sedimentation rate and particulate rain.The burial fraction of BSiO2 is small relative to benthic rain (5–19%). Despite the small fraction buried, burial flux normalized to (sedimentation rate)1/2 appears to provide a very consistent means of predicting benthic particulate rain over a large range of rain rates, including data from a number of different studies and environments. At sites with BSiO2 rain 250 mmol m−2 yr−1 the average difference between predicted and observed rain is 25–30%. Such rain rates occur in many marine areas, particularly the Southern Ocean, with the result that this relationship potentially provides a means of estimating BSiO2 benthic rain over prolonged periods in the past on the basis of readily measured sediment parameters.At the southern-most deep ocean station, the particulate flux was characterized by an extremely high Corg/CaCO3 ratio (>10), but this high ratio does not appear to have a substantial influence on CaCO3 burial. CaCO3 is preserved in the sediments at this site despite a particulate flux with a 10-fold excess of Corg above that required for complete dissolution in the sediments. The unexpectedly high preservation of CaCO3 is due largely to the very steep Corg oxidation rate profile at this site. As a result, a large fraction of the organic matter oxidized in the sediments does so in close proximity to the sediment–water interface where most of the metabolic CO2 is neutralized by CO32− from the overlying water, rather than by the dissolution of sedimentary CaCO3.Diagenetic modeling indicates that at several of the stations, the remineralization fluxes of carbonate species across the sediment–water interface may not have been at steady state as a result of the highly pulsed nature of particulate rain in this environment. We estimate that at the time of our sampling it is possible that near-interface fluxes could have been a factor of 1.6–2 times the annual average.At every site on the transect, the burial fluxes of detrital material are substantially greater than the detrital particulate rain measured in the sediment traps, by as much as a factor of 40. Detrital burial is bimodal, being greatest at the southern and northern extremes of the transect. We postulate that the excess of burial over particulate rain in the south reflects the contribution of ice rafted debris at these high latitudes. Increases in the supply at the northern stations must have a different source. We believe that the excess at these stations is material eroded from the sea floor to the west, possibly on the Campbell Plateau, and advected by currents to the northern portion of the transect at depths below the shallow traps.  相似文献   

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