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1.
Research is conducted on the following questions: 1) the seasonal and spacial changes of Fe2+ concentration in overlying water and interstitial water; 2) the profiles of Fe3+ and Fe2+and total Mn in solid phase of sediment; and 3) the estimation and comparison of Fe and Mn diffusion and deposition fluxes.The complex relation among the early diagenesis of iron, the grain size composition in solid phase of sediment and the factors of pH and Eh as well as dissolved oxygen are reflected by seasonal and space relation of Fe2+ change.The geochemical activity and role of iron and manganese during diagenetic processes is discussed and estimated by calculating and comparing deposition and diffusion fluxes of both the elements. 相似文献
2.
1985年12月至1986年4月对西太平洋锰结核进行了调查并对所获沉积物样品进行了分析,研完了锰结核区域沉积物中Fe,Mn,Al和CaCO_3的含量分布特征及其相关关系,说明沉积物中Fe,Mn,Al和caCO_3的含量分布特征主要受水深的制约。 相似文献
3.
2007年11月在东海泥质区采集了表层沉积物样品,用连续提取法对金属元素的赋存形态进行了分离,测定了各形态中锰、铁和铝的含量。结果表明,锰主要赋存于碳酸盐结合态,含量为0.04～0.19mg/g,平均0.13mg/g;铁主要赋存于易还原态(铁锰氧化物结合态),含量为1.1～2.3μg/g,平均1.5mg/g;大部分站点的铝主要赋存于易还原态,含量为0.4～1.1mg/g,平均0.7mg/g。沉积物主要成分对金属赋存形态产生影响,CARB态、ERO态Mn、Fe和Al分别随沉积物中碳酸钙、水合铁锰氧化物含量的升高而增加,且ERO态金属与水合铁锰氧化物的相关性显著;有机物的含量的对OSM态金属的影响则不明显。非残渣态Fe和Al的含量随水深增加而降低,主要是由于沉积物中ERO态Fe和Al受陆地径流输入和水体中清除作用的影响,导致近岸沉积物中有较多的活性Fe、Al;离岸距离增加则沉积物中活性Fe、Al含量减少。 相似文献
4.
The horizontal and vertical distributions of manganese in sea water, interstitial water and sediments in the Hiro Bay, Seto Inland Sea, Japan, have been investigated. The outflow from a pulp mill is the primary source of manganese in this bay. The industrial waste water contained 0.19 mg l–1 of manganese, mostly in a dissolved form. This manganese diffused out both horizontally and vertically into the surrounding sea water. The content of manganese in the liquid and solid phases in the sediments, however, are inverse with that in the sea water; namely the lowest concentration of manganese in the sediments was observed at the station near the outfall and manganese concentration increased with the distance from the outfall. 相似文献
5.
S. Knox W. J. Langston M. Whitfield D. R. Turner M. I. Liddicoat 《Estuarine, Coastal and Shelf Science》1984,18(6):623-638
By combining field observations with a statistical approach and a simple but effective estuarine analogue, the main features of the cycling of arsenic in the Tamar estuary have been elucidated. As(III) and As(V) enrichment in the water column is due to a combination of localized inputs and effective recycling of sediment interstitial waters. The profiles of As(V) are similar to those of NH4+ and are dominated by an estuarine maximum resulting from an input from the sediments. As(III) profiles are correlated with those of dissolved manganese and exhibit both fresh water and estuarine maxima. As(III) appears to be effectively removed at the freshwater/brackish water interface by a combination of heterogenous oxidation, catalysed by hydrous manganese dioxide, and adsorption on to iron oxyhydroxide. The estuarine distribution of As(III) within the water column is consistent with the published rates of oxidation of As(III) to As(V) by both inorganic and microbiological processes. The reduction of As(V) to As(III) in the sediments is incomplete. On the basis of our observations a tentative estuarine arsenic cycle is presented. 相似文献
6.
The effect of benthic oxygenic photosynthesis on sediment-water fluxes of manganese and iron was studied for an intertidal sediment. Undisturbed sediments were incubated at an incident surface irradiance of 250 μE m−2 s−1at 26 °C. Oxygenic photosynthesis was selectively inhibited by adding [3-(3,4-dichloro)-1,1-dimethyl-urea] (DCMU). Benthic fluxes were determined experimentally from the change in manganese and iron concentrations in the overlying water, and were predicted from the pore water concentration gradients at the sediment-water interface assuming molecular diffusion as the transport mechanism. The experimental fluxes of manganese and iron in DCMU-treated cores amounted to −0·84 and −0·59 mmol m−2day−1, respectively, and were directed from the sediment towards the overlying water. In the control cores, showing high rates of benthic oxygenic photosynthesis, the fluxes of manganese and iron were directed towards the sediment, 0·06 and 0·01 mmol m−2day−1, respectively. Mass balances for the 0·1–0·14 cm thick oxic zone, calculated from the experimental fluxes and the predicted fluxes, suggest a minimum areal reoxidation of 0·6 mmol m−2day−1for manganese and of 0·48 mmol m−2day−1for iron in cores showing benthic photosynthesis. The estimated turnover times for dissolved Mn2+and dissolved Fe2+in the oxic surface layer during benthic photosynthesis were 0·8 and 0·25 h, respectively. Sediment oxygen microprofiles and the sediment pH profiles suggest that chemical precipitation and reoxidation dominates the retention of manganese and iron during benthic oxygenic photosynthesis in shallow intertidal sediments. 相似文献
7.
综述了天然气水合物赋存区甲烷渗漏活动的地球化学响应指标的研究进展,分析了应用单一指标识别甲烷渗漏活动各自所存在的问题,包括浅表层沉积物孔隙水中CH_4、SO_4~(2–)、Cl~–等离子浓度随深度的变化;浅层沉积物全岩W_(TOC)(W表示质量分数,TOC表示总有机碳)和W_(TS)(TS表示总硫)之间的相关性及比值;自生碳酸盐岩δ~(13)C和δ~(18)O;自生矿物重晶石、黄铁矿、自生石膏的δ~(34)S;有孔虫壳体和生物标志化合物的δ~(13)C等。结果表明孔隙水中的CH_4、SO4_~(2–)浓度及溶解无机碳的碳同位素组成可以用来识别目前正在发生的甲烷渗漏活动;而沉积物中的WTS、自生矿物的δ~(34)S、钡含量及其异常峰值和生物标志化合物的δ~(13)C等指标的联合使用可以更真实准确地反映地质历史时期天然气水合物赋存区的甲烷渗漏活动。因此,在实际研究过程中,可将孔隙水和沉积物两种介质的多种指标相结合。随着非传统稳定同位素(Fe、Ca、Mg等)和沉积物氧化还原敏感元素(Mo、V、U等)等研究的发展,甲烷渗漏活动地球化学响应指标的研究也将得到拓展,而多种地球化学指标的联合使用将为天然气水合物勘探及其形成分解过程识别研究提供重要的科学依据。 相似文献
8.
Parke A. Rublee Susan M. Merkel Maria A. Faust 《Estuarine, Coastal and Shelf Science》1983,16(5):501-509
The number of bacteria in sediments, interstitial water and overlying tidal water of an oligohaline marsh system are about 109, 106 and 106 cells cm?3, respectively. Average cell size in the overlying water (about 0·06 μm3), is much smaller than that in sediments and interstitial water (about 0·18 μm3). Most bacterial cells in sediments are bound to sediment particles and less than 1% of the cells were displaced by percolating water through sediment columns. Concentration of bacteria in flooding tidal waters is generally higher than that in ebbing waters. Movement of bacterial biomass does not appear to be a significant mechanism of particulate organic transport in marsh sediments and marsh sediments do not appear to be a source of suspended bacteria for estuaries. 相似文献
9.
The authors have determined the distributions of Ph, Cu and Cd ia surface sediment, acid-soluble fraction and interstitial water of the Changjiang Estuary and analysed the relationship between them and some environmental parameters, finding that there exists a quasi-equilibrium between the interstitial water and the sediment. The distribution of Pb or Cu in both phases it controlled mainly by the adsorptioa-desorption and deposition-solution processes of HFO" and org." in the sediments, whereas Cd is mainly controlled by the depoahisn-Jolution process of CdS. The sedimentation mechanism of Ph, Cu and Cd in the Changjlang Estuary is preliminarily proposed. 相似文献
10.
The magnitude of the exchange flux at the water–sediment interface was determined on the basis of the ammonia concentration gradient at the near-bottom water–interstitial interface and Fick's first law. It was established that in Puck Bay, ammonia almost always passes from the sediment to water. Ammonia flux varied from 5 to 1434 μmol NH4-N m−2 day−1. In total,c. 138·2 tonneammonia year−1pass from sediments of Internal Puck Bay to near-bottom water, the equivalent value for External Puck Bay being 686·9 tonne year−1. In total, about 825 tonne ammonia year−1passes from the sediment to near-bottom water of Puck Bay. In interstitial waters, ammonia occurred in concentrations varying over a wide range (3–1084 μmol NH4-N dm−3).The basic factors affecting the magnitude of ammonia concentration in interstitial waters included: oxidation of organic matter, type of sediment, and inflow of fresh underground waters to the region examined.This paper involves preliminary studies only and constitutes a continuation of the studies on ionic macrocomponents and phosphorus in interstitial waters of Puck Bay undertaken previously. 相似文献
11.
The contents of Fe, Mn, Cu, Co, Ni, Pb and Zn in the seaiment associated with manganese nodules from the Northern Central Pacific Ocean and in their acid-soluble fractions were determined and correlations among the elements and between the trace metals and environmental parameters were discussed. It has been found that the contents of Mn, Cu and Ni in the sediment are one order of magnitude higher than those in the common sediment. As shown in the manganese nodules, they may mainly derive from seabed. The contents of all trace metals in the sediment are obviously governed by Fe-and Mn-oxides, organic matter, seawater depth, particle size and Eh. Multi-element correlation equations were developed for all trace metals. The trace metals in acid-soluble fraction of the sediment were also much higher than ihose of common sediment and negatively correlated with water depth, implying the possible influence of carbonate speciation. 相似文献
12.
Svetlana V. Pakhomova Per O.J. Hall Mikhail Yu. Kononets Alexander G. Rozanov Anders Tengberg Andrei V. Vershinin 《Marine Chemistry》2007
Fluxes of dissolved forms of iron and manganese across the sediment–water interface were studied in situ in the Gulf of Finland and the Vistula Lagoon (Baltic Sea), and in the Golubaya Bay (Black Sea) from 2001 to 2005. Fluxes were measured using chamber incubations, and sediment cores were collected and sliced to assess the porewater and solid phase metal distribution at different depths. Measured and calculated benthic fluxes of manganese and iron were directed out of sediment for all sites and were found to vary between 70–4450 and 5–1000 µmole m− 2 day− 1 for manganese and iron, respectively. The behavior of the studied metals at various redox conditions in the near-bottom water and in the sediment was the main focus in this study. Our results show the importance of bottom water redox conditions for iron fluxes. We measured no fluxes at oxic conditions, intermediate fluxes at anoxic conditions (up to 200 μmole m− 2 day− 1) and high fluxes at suboxic conditions (up to 1000 μmole m− 2 day− 1). Total dissolved iron fluxes were generally dominated by iron(II). Contribution of iron(III) to the total iron flux did not exceed 20%. Obtained fluxes of manganese at all studied regions showed a linear correlation (r2 = 0.97) to its concentration in the porewater of the top sediment layer (0–5 mm) and did not depend on dissolved oxygen concentrations of bottom water. Organically complexed iron and manganese were in most cases not involved in the benthic exchange processes. 相似文献
13.
The interstitial water composition (
, alkalinity, Ca2+, Mg2+, Sr2+, Na+, K+) and the cation exchange capacity (CEC) were determined for the muddy sediments of the continental shelf off the Gironde Estuary (France), in the area where the sediment represents the deposit of the muddy suspension of the river. In comparison with seawater concentrations, the pore waters below 10 cm depth, show depletions of
and Ca2+ and below a 30 cm depth show depletions of Mg2+. Inversely, the upper 10 cm an enrichment of Ca2+ concentration, and an increase of K+ concentration to a 40 cm depth. High values of
are observed at the top 4 cm. Alkalinity enrichment is observed along the length of the core. Applying the alkalinity models for the sediment below a 10 cm depth demonstrates generally that calculated alkalinities are higher than the measured ones. Ca2+ dissolution occurs at the first 10 cm and authigenic carbonate precipitation starts beneath that level. Mg2+ depletion is accompanied by bicarbonate loss. This proves that Mg2+ depletion is due to a Mg-silicate reaction. The result of the CEC does not confirm the Mg2+ uptake by clay minerals in exchangeable site, under reducing conditions. Diffusion and bioturbation play an important role in the pore water concentration at the top of the core. 相似文献
14.
15.
本文通过对中太平洋海盆４０多个表层沉积物的分析和研究，根据沉积物中各组分含量、物质来源和成因等特征，把本区表层沉积物分为六种类型。它们分布在不同区域和不同水深范围内。钙质沉积物分布在碳酸钙补偿深度（ＣＣＤ）界面以浅区。硅质粘土、深海粘土等沉积物出现在ＣＣＤ以下水深区，这些沉积物的分布具有明显的垂向分带性和横向分区性。沉积物类型的变化主要受水深与物质来源的控制，南极底层流也有一定的影响。在不同的沉积物中锰结核的丰度、品位、类型等亦有明显的差异。 相似文献
16.
Diagenetic deposition of manganese in sediment of a historically meromictic lake,Lake Suigetsu,Japan
Vertical profiles of manganese concentration in interstitial waters and of manganese and iron contents in five chemically-separated fractions of sediments have been studied in a sediment core (73 cm long) from a meromictic lake, Lake Suigetsu, which changed from freshwater to brackish conditions in 1664 A.D. The interstitial waters show a minimum manganese concentration of 0.13 ppm near a depth of 10 cm and a maximum of 26 ppm near 65 cm in the core. A predominant amount of manganese, up to 0.17%, is found in the hydrogen peroxide-soluble fraction of sediments in layers above a depth of 52 cm. It is suggested that the manganese is included in stable iron sulfides such as pyrite. Manganese, which diffuses upward from the lower layer, is thought to be deposited along with stable iron sulfide during diagenetic formation of the latter near a depth of 10 cm in the core. 相似文献
17.
F.T. Short M.W. Davis R.A. Gibson C.F. Zimmermann 《Estuarine, Coastal and Shelf Science》1985,20(4):419-430
The seagrass Syringodium filiforme was examined in an ecological analysis of plant nutrient requirements and nutrient resource availability. Assessment of the sediment geochemistry in a San Salvador Island seagrass bed indicated that phosphorus was not readily accessible to the plants. Ammonium regeneration in the fine-grained carbonate sediments was high, and interstitial concentrations averaged ca. 100 μM while phosphate replenishment to interstitial water was low, and concentrations were generally less than 2 μM. Analysis of the seagrass leaf tissue content (C : N : P = 1390 : 47 : 1, atomic wt) suggested that nitrogen and phosphorus were both depleted relative to carbon. However, this high N : P for S. filiforme and the low concentration of phosphate available in the interstitial water established the likelihood that plant acquisition of phosphorus was limited. The finding of high root biomass relative to leaf biomass in these seagrass beds corroborates this evidence by depicting a method of plant adaptation that increases nutrient absorptive root surface area. 相似文献
18.
Bacterial iron oxide reduction in a terrigenous sediment-impacted tropical shallow marine carbonate system, north Jamaica 总被引：1，自引：0，他引：1
Kevin G. Taylor Christopher T. Perry Anthony M. Greenaway Philip G. Machent 《Marine Chemistry》2007,107(4):449-463
Discovery Bay, a carbonate-dominated embayment in north Jamaica, has been subject to inputs for 40 years of iron-rich bauxite sediment associated with the local mining and transport of processed bauxite. As such, this site is an ideal natural laboratory to study the records and impacts of iron oxide inputs upon geochemical, diagenetic, and microbial processes in tropical carbonate sediments.Total Fe contents in sites in the bay not receiving bauxite inputs are negligible and porewater Ca2+, SO42− and Cl− indicate that bacterial sulphate reduction is an important process. In contrast, surface sediments receiving bauxite inputs contain significant total Fe, from 44 μmol/g in shallow (5 m water depth) sites to 110 μmol/g in deeper (20 m water depth) sites. Up-core increases in total Fe record increased temporal inputs into the bay. Within these Fe-rich sediments porewater data shows the presence of FeII released by bacterial FeIII reduction. There is no direct evidence for significant bacterial sulphate reduction in these sediments. Iron oxides within all bauxite-impacted sediments display a high potential reducibility, from 40% to 80% of the total Fe present as dithionite-extractable FeIII. Experimental analysis of the potential susceptibility to, and rates of, bacterial FeIII reduction, utilising Discovery Bay sediment and Shewanella putrefaciens CN32 (a known FeIII-reducer) has confirmed the high bacterial reducibility of iron oxides within the sediment. Up to 75% of initial dithionite-extractable FeIII in the sediments was reduced over 15 days.The presence of iron oxides within the Discovery Bay shallow marine carbonate systems has markedly altered the chemical diagenetic processes taking place, with a shift from apparent dominance of bacterial sulphate reduction at non-impacted (Fe-poor) sites, to highly significant bacterial FeIII reduction in Fe-rich bauxite-impacted sediments. Given the perceived global increases in terrigenoclastic sediment inputs into tropical carbonate systems as a result of land-use and climate changes, coupled with the documented role that iron oxide reduction plays in nutrient and contaminant cycling in sediment systems, more research into the perturbation of early diagenesis by iron oxide inputs is required. 相似文献
19.
H. Elderfield 《Marine Chemistry》1976,4(2):103-132
Application of a simple model describing regional variations in the contents of manganese and associated minor metals in deep-sea sediments suggests that solid manganese phases are being removed from the <0.5 μm fraction of seawater at ～1–7 · 1012g yr?1 in excess of the rate of stream-supplied manganese. This flux is consistent with: (1) the relative rates of sediment accumulation in the Atlantic and Pacific Oceans; (2) the contrast between the oceanic residence time of manganese calculated from stream-supply data (14 · 103 yr) and from the flux of manganese precipitating in marine sediments or as manganese nodules (0.38–2.4 · 103 yr); (3) the surplus mass of manganese revealed by geochemical balance calculations (22.9 · 102g). On this basis excess manganese is accumulating in deep-sea sediments at 0.2–2.0 · 10?6 g cm?2yr?1. Manganese supplied to the upper layers of marine sediments by diagenesis has been evaluated with the aid of vertical advection—diffusion—reaction models. The calculated diagenetic flux of manganese at the sediment surface in a near-shore environment is in agreement with the known accretion rate of manganese deposits (1.7 · 10?2 g cm?2 10?3 yr?1) and the regionally variable flux over the area assessed is consistent with the presence or absence of manganese nodules at or near the water-sediment interface. The diagenetic flux at the surface of deep-sea sediments has been calculated at 0.7 · 10?4 g cm?2 10?3 yr?1 when the upper, oxic, zone of the sediment is ～20 cm thick. A limiting factor on the in situ production flux of dissolved manganese in deep-sea sediments appears to be the availability of reducing agents for manganese dissolution rather than the rate of downward transport of manganese-rich sediment to a reaction boundary where dissolution takes place. Various estimates of the rate of upward-migrating manganese suggest that manganese precipitates in the oxic zone with a rate constant of ～10?7 sec?1 with the result that diagenetic processes cannot supply the flux of excess manganese through more than ～0.25 m of oxic sediment. However, estimates of the flux of manganese to the oceans by submarine volcanic processes (0.79–1.1 · 1012g yr?1) are similar to the surplus mass of manganese detected by geochemical balance calculations (0.7 · 1012g yr?1). If submarine hydrothermal solutions provide only 10% of this excess then their computed discharge rate (39 g cm?2 yr?1) and residence time in the upper layer of oceanic crust (130,000 yr) agree well with these parameters for continental thermal springs. 相似文献
20.
沉积物中氧化还原敏感元素(Redox Sensitive Element,RSE)含量变化是上覆水体氧化还原环境良好的替代指标。本文通过冲绳海槽中南部两个柱状沉积物(深度：30 cm)粒度、总有机碳、总氮及其同位素含量和氧化还原敏感元素含量等指标,探究复杂环境背景下冲绳海槽柱状沉积物中RSE的赋存机理与环境指示意义。研究发现,柱状沉积物中除了Cr亏损,其他RSE均显示有不同程度的富集。“粒控效应”对冲绳海槽柱状沉积物的RSE含量影响较小;分析可知,海水表层生产力是影响沉积物氧化还原环境的主要因素,通过Mn(氢)氧化物的吸附或解吸附作用实现RSE的富集与亏损。δCe、V/Cr、Ni/Co和V/(V+Ni)等指标指示沉积物整体处于氧化-弱氧化环境。沉积物中Mn元素通过还原作用以Mn2+形式向上扩散,在25～30 cm处被含氧间隙水氧化富集形成锰峰,指示柱状沉积物0～25 cm处为氧化环境,25～30 cm处为弱氧化环境。 相似文献