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1.
The metal load into sediments and the change in the sedimentary environment of Osaka Bay in the Seto Inland Sea have been studied through geochemical analysis of core sediments, using both Pb-210 dating and a selective chemical leaching technique. Analytical results from a 6-m core of sediment show that copper and zinc pollution started in the late 1800's and the present enrichment ratios of copper and zinc, relative to background levels (20 mg kg–1 for Cu and 94 mg kg–1 for Zn), are 2.8 and 4.1, respectively. The present anthropogenic copper and zinc loads into Osaka Bay sediments, are 47 and 368 ton yr–1, while natural copper and zinc loads are 40 and 186 ton yr–1, respectively. Osaka Bay sediment at the present day is considered to be seriously polluted by zinc, now. The vertical profiles of copper and zinc in four successively separated fractions (10% acetic acid soluble fraction: F-HAC, 0.1M hydrochloric acid-soluble fraction: F-HCl, hydrogen peroxide-soluble fraction: F-H2O2 and hydrofluoric acid-soluble fraction: F-HF) from the core sediments indicate that enrichments of copper and zinc in the upper layer of the sediment are dependent on increases in the metal contents of the F-HAC, F-HCl and F-H2O2 fractions. Copper in F-HAC, and zinc in F-HAC and F-HCl, seem to be of anthropogenic origin.Results of sequential studies of the whole Seto Inland Sea can be summarized as follows: At the present time, the sedimentary loads of copper and zinc over the whole Seto Inland Sea area are 630 and 3,500 ton yr–1, respectively, while the natural and anthropogenic loads are 320 and 310 ton yr–1 for copper and 1,800 and 1,700 ton yr–1 for zinc, respectively. 相似文献
2.
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
3.
Selective chemical attack has been used to separate recent surface marine sediments into organic, non-detrital and detrital components, and the concentrations of iron, manganese, copper and zinc in each fraction determined. The non-detrital fraction controlled the overall elemental concentrations and relationships apparent in the bulk sediment, particularly in the cases of copper, manganese and zinc. Copper was found associated with the organic fraction. The predominant processes of primary deposition are precipitation of hydrated ferric oxide and adsorption of copper and zinc onto this material. 相似文献
4.
Shizuko Hirata 《Marine Chemistry》1985,16(1):23-46
Phosphorus and metals bound to organic matter were separated from coastal sediments of Harima Sound in Seto Inland Sea, Japan by extraction with NaOH and fractionated by Sephadex G-25 chromatography. Phosphorus and metals were determined in the eluates by a multi-channel, inductively coupled plasma-atomic emission spectrometer. Phosphorus and Cu, Zn, Fe, Mn, Ni, Cr, Co and Ti bound to organic matter with high molecular weights (OMHMW) (MW ? 5000) were found to be present in the sediments, but no Mo or V were found. The technique provides minimum estimates of the amounts of P and metals bound to organic matter. These organic complexes show surface enrichment in a sediment core (0–20 cm) and their contents decrease with depth. Also, the amounts of eighteen elements, namely: P, Fe, Mn, Zn, Cu, Si, Al, Ti, Pb, Co, Ni, Cr, Mo, V, Na, K, Ca and Mg, in H2O, ammonium acetate at pH 7 and 5, hydrogen peroxide, hydroxylamine hydrochloride and hydrogen fluoric acid soluble fractions have been determined with a selective chemical leaching technique for the 210Pb-dated sediment core sample. Considerable amounts of P (6–19%) and Cu (5–21%) were associated with organic matter, in contrast to other metals such as Fe, Mn, Zn, Ni, Cr, Co and Ti which were associated with sulfide and silicate. 相似文献
5.
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
6.
基于PXRF的西南印度洋脊硫化物表层沉积物地球化学找矿研究 总被引：3，自引：0，他引：3
海底热液喷发形成的热液羽状流中富含成矿物质,并沉淀在距离热液喷口不等的范围内。对西南印度洋中脊热液喷口附近、距离喷口中等距离、远离喷口的六个表层沉积物样品开展了不同粒度沉积物的便携式XRF（PXRF）分析。结果表明,PXRF可以有效获得的洋中脊钙质沉积物中成矿元素的富集特征。>40目的沉积物样品具有较高的Cu、Zn、Fe、Mn等元素含量,40目以下沉积物中则相对稳定,可能与粗粒沉积物中玄武岩碎屑/玻璃含量较高有关,与镜下鉴定结果一致。以热液喷口为中心,表层沉积物中表现出Cu、Zn、As、Fe、Mn的元素分带,靠近喷口的沉积物中具有较高的成矿元素的含量,并具有较高的Cu/Fe、Zn/Fe比值或者Cu/Mn与Zn/Mn比值。上述结论表明,洋中脊沉积物中成矿元素的含量主要受与喷口的距离的影响,而与粒度的关系不大,洋中脊沉积物地球化学找矿应采用40目以下粒径沉积物作为分析样品。通过PXRF获得的Cu、Zn、As、Fe、Mn等元素含量及其比值特征可以作为海底多金属硫化物沉积物地球化学找矿的指标,该方法满足快速有效识别洋中脊沉积物中地球化学异常的要求。 相似文献
7.
8.
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. 相似文献
9.
Vertical distributions of sulfate, hydrogen sulfide, and iron (II) concentrations in interstitial waters and of sulfur content in sediment have been studied in a sediment core (73 cm long) from a meromictic lake, Lake Suigetsu, which changed from fresh-water to brackish conditions in 1664 A.D. The diatom assemblage of the sediment has also been analyzed. A boundary between high (>1.5%) and low (<0.2%) sulfur contents is found at a depth of 52 cm in the core. In the high sulfur layer (above 52 cm), the maximum sulfur content is 6.8% at 35 to 37 cm. The diatom assemblage, however, indicates that the boundary between fresh-water and brackish sediments lies at 40 cm. The hydrogen sulfide and iron (II) profiles in the interstitial waters indicate a sink for these chemical species near a depth of 40 cm. The discrepancy between the chemically-defined boundary at 52 cm and the paleontologically-defined boundary at 40 cm seems to be due to the downward migration of hydrogen sulfide and deposition of iron sulfide after the lake became brackish. 相似文献
10.
The distribution of molecular masses of organic ligands for copper(II) in oceanic water was investigated. The bulk dissolved organic matter (DOM) was fractionated by ultrafiltration and organic ligands were extracted from the resultant fractions by using immobilized metal ion affinity chromatography (IMAC). Contributions of total organic ligands were 2.0–4.4% of the bulk DOM in surface waters, as determined by the UV absorbance. In the distribution of molecular masses of organic ligands, relative contribution of the fraction with low molecular masses (<1000 Da) was dominant (49–62%), while 26–33% of the total organic ligands was in the 1000–10,000 Da fraction, leaving 10–19% in the >10,000 Da fraction. The distribution of molecular masses of organic ligands shifted to higher molecular masses, as compared with that of the bulk DOM. The fluorescence intensities of organic ligands were shown to be associated with carboxyl contents, based on peak excitation/emission wavelengths and the pH-dependence of fluorescence. Two ligand classes with different conditional stability constants (log KCuL′≈7 and 9) were determined from fluorescence quenching of ligand fractions during copper(II) titration. Organic ligands in low molecular mass fractions were relatively weak and strong ligands occurred in higher molecular mass fractions. It is suggested that the weaker ligand sites would consist of two or more carboxyl groups (log KHL′=4), whereas carboxyl groups (log
=2), which are protonated at lower pH, and primary amine may additionally contribute to the formation of more stable copper(II) complexes of the stronger ligand. 相似文献
11.
In the Hiuchi-Nada area of the Seto Inland Sea, Japan, sedimentation rates were determined with the Pb-210 technique, and heavy metals in sediments were also analyzed. Sediments were collected in twelve short sediment cores and a long sediment core, using 1-m and 6-m gravity corers.The sedimentation rates vary from 0.14 to 0.31 g cm–2yr–1. The highest sedimentation rate was observed in the central part of the area, while lower sedimentation rates were observed in the eastern part.In Hiuchi-Nada, a remarkable increase in copper and zinc contents is noticeable as early as the 1800's. Over the past 240 years a copper smelter at the south-western side of this area has been causing serious pollution of the sediment. Now, anthropogenic copper and zinc loads into the sediment are 123 and 376 ton yr–1 compared to natural copper and zinc loads of 82 and 401 ton yr–1, respectively. The highest level of copper and zinc pollution was observed in the 1960's, when the relative enrichments above background values (copper; 19 and zinc; 93 mg kg–1) were 5.5 and 2.8, respectively. 相似文献
12.
Dissolved electroactive concentrations of zinc, cadmium, lead and copper in river Rhine and North Sea samples have been measured at natural and lower pH values by differential pulsed anodic stripping voltammetry using a Kemula-type hanging mercury drop electrode. Average concentrations detected in North Sea samples at salinities and their range are (in μgl?1): 3.9 (2.0–7.5) for zinc, 0.23 (0.13–0.31) for cadmium, 0.3 (0.1–0.6) for lead and 0.3 (0.25–0.60) for copper (pH 8.1). The APDC-MIBK extracting/concentrating method, followed by AAS measurement applied to the same samples, resulted in 3.9 (2.0–7.5) for zinc, 0.11 (0.01–0.27) for cadmium, 0.5 (0.2–0.9) for lead and 1.6 (0.7–3.2) for copper. A fraction of the electroactive concentrations at pH 2.7 (6.1 for Zn) is electroactive at pH 8.1. The fractions are 100% for Cd, 20% for Cu, 13% for Pb and 40% for Zn. The remaining fractions are partly composed of organically bound species in solution. The low value for lead may be caused by the presence of particulate lead that is dissolved at low pH.Ionic copper and lead species, added separately to seawater at pH 8.1 are removed from the electroactive form, and taken up in (organic) complexes in the same ratio (at least for copper) as the species already present. Added ionic zinc is not removed within the time scale of the measurements (30 min). North Sea water at the natural pH has a complexing capacity, probably due to the presence of dissolved organic compounds, in a concentration equivalent to 3.10?7M copper. The complexing capacity is zero at pH 2.7. The usual method of standard addition for the determination of electroactive copper and lead concentrations may lead to erroneous results in samples where complexation of this type occurs. 相似文献
13.
The variations in CaCO3 and organic carbon and their inter-relationship in a core from the southeastern Arabian Sea (water depth 2,212 m) have been
used to demarcate the Holocene/Pleistocene boundary; an increased terrigenous deposition during Late Pleistocene has been
inferred. The higher contents of organic carbon and sulfide sulfur and their negative relationship clearly establish the existence
of a reducing environment below 65 cm subbottom depth. The occurrence of pyrite framboids and crystals, present only on the
surface of fecal pellets (80–85 cm), has been discussed in terms of significance of reducing microenvironment. 相似文献
14.
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
15.
Joan D. Willey 《Marine Chemistry》1977,5(3):267-290
Dissolved silica can coprecipitate with zinc from seawater or distilled water that has been enriched with both elements. More than 2 ppm Si are necessary for the reaction to begin. The coprecipitation shows pH dependence. The addition of pulverized illite or natural sediment as suspended particulate material does not enhance the reaction in seawater. The organic material present in the nearshore seawater samples decreases the rate and extent of reaction, as indicated by comparisons of results of experiments using natural seawater with results obtained using UV-irradiated seawater. In unbuffered distilled water the reaction must compete with hydrolysis of zinc; however, reaction does occur, which indicates that the seawater matrix is not essential for the reaction. The coprecipitation can limit the concentration of zinc in seawater to less than the solubility concentration assumed for ZnCO3 or Zn(OH)2. The results suggest that a zinc silicate can precipitate directly from seawater or interstitial water as an authigenic mineral. 相似文献
16.
东海泥质区表层沉积物中铜和铅的赋存形态研究 总被引：1，自引：0，他引：1
2007年11月在东海泥质区13个站点采集了表层沉积物样品,用连续提取法分离并测定了铜和铅的赋存形态。结果表明,铜主要赋存于易还原态(铁锰氧化物结合态),含量为1.2～5.1μg/g,平均值为3.3μg/g;铅主要赋存于碳酸盐结合态,含量为1.9～7.3μg/g,平均值为5.3μg/g。泥质区铜和铅的有机结合态和易还原铁锰氧化物结合态与水深之间的呈明显的相关关系,碳酸盐结合态则与水深不相关。铜和铅非残渣态总量与采样站点水深之间的关系受控于其主要赋存形态,反映了重金属形态分布受到陆源输入和在水体中迁移等因素的影响。济州岛西南泥质区表层沉积物中铁锰氧化物结合态的铜和铅含量高于其他海区表层沉积物,可能是由于沉积物再悬浮所致。 相似文献
17.
研究了滇池螺蛳(Margarya melanioides)分布和底泥营养成分之间的关系。2013年在滇池87个采样点采集螺蛳和底泥样本,图示分析所有采样点的活的螺蛳数量,确定活螺在滇池中的分布位点及分布密度;选择8个采样点的底泥样本,进行16项营养元素(有机质、磷、氮、锌、铁、锰、镁、钙、铜、钠、钾、砷、汞、铅、镉、铬)含量测定,分析这些样本营养元素的差异。根据这8个采样点中有无螺蛳生长,将8个底泥样本分为两组,采用完全随机设计两样本比较的t检验,结果两组样本间仅铜的含量有统计学差异(P0.05),这可能是由于滇池螺蛳的生长有效富集了重金属铜元素,使有螺区域比无螺区域底泥中铜的含量明显减少。这在一定程度上说明了螺蛳生长与底泥的关系,可为滇池污染防治及螺蛳种群保护提供相关的科学依据。 相似文献
18.
渤海中部表层沉积物中重金属赋存相态及来源 总被引：1，自引：1，他引：0
近年来由于环渤海经济圈的快速发展,渤海接受了来自周边河流、沿岸排污及海上油气开采所产生的大量的重金属等污染物质,使得渤海的生态环境系统面临前所未有的压力。本文采用电感耦合等离子质谱仪（ICP-MS）对采自渤海中部的25个表层沉积物样品中的Cu、Co、Ni、Zn、Pb、Cr、Cd等重金属元素的含量和赋存相态进行了分析,探讨了重金属分布规律、污染状况及来源。研究结果表明,Cu、Co、Ni、Zn、Cr在渤海湾的近岸区域和渤海中部泥质区有较高的含量,而Pb和Cd则在整个研究区的含量都较高;表层沉积物中Cu、Co、Ni、Zn、Cr主要以残渣态形式存在,而Pb和Cd则具有较高的非残渣态含量;生态风险评价结果表明该区表层沉积物未受到Co、Ni、Cr的污染,Cu、Zn、Pb和Cd则为未污染-中等程度污染。重金属元素Co、Ni、Cr以自然来源为主,在沉积物中的分布主要受沉积物物质组成的影响,而Cu、Zn、Pb,尤其是Cd,则受到了人类活动的显著影响。黄河沉积物是研究区表层沉积物中重金属的主要来源,影响范围涵盖了本区大部分区域,但在研究区的北端受到滦河来源物质的影响,渤海湾和研究区中部则受到海河物质和大气沉降来源重金属的一定影响。 相似文献
19.
Fifteen recent sediment samples from the offshore Orinoco Delta, Venezuela, were separated by sieving and pipette analysis into seven size fractions ranging from 4ø to 10ø, in 1 ø units. Total organic carbon was determined for each size fraction and the organic matter characterized by pyrolysis and pyrolysis-gas chromatography. The sediments average 0.98% organic matter with somewhat higher values nearshore. Nearshore sediments also had higher organic contents in the coarsest fractions and a decrease in organic matter from coarse to fine sediment fractions. Sediments from further offshore generally show the highest organic contents in the finer fractions. Pyrolysis showed a low bitumen content and confirmed that the kerogen was dominantly terrestrial and gas prone. The observed trends were attributed to sorting of organic matter by its physical characteristics, with the denser, coarse-grained material settling out nearshore and the Finer-grained material being carried further from shore and settling out with finer-grained sediments. 相似文献
20.
Aurélia Mouret Pierre Anschutz Bruno Deflandre Gwénaëlle Chaillou Christelle Hyacinthe Jonathan Deborde Henri Etcheber Jean-Marie Jouanneau Antoine Grémare Pascal Lecroart 《Deep Sea Research Part I: Oceanographic Research Papers》2010,57(4):528-540
The relationship between particulate organic carbon (POC) concentrations measured in modern sediment and fluxes of exported POC to the sediment surface needs to be understood in order to use POC content as a proxy of paleo-environmental conditions. The objective of our study was to compare POC concentrations, POC mineralization rates calculated from O2 consumption and POC burial rates. Benthic O2 distributions were determined in 58 fine-grained sediment cores collected at different periods at 14 stations in the southeastern part of the Bay of Biscay with depths ranging from 140 to 2800 m. Depth-dependent volume-specific oxygen consumption rates were used to assess rates of aerobic oxidation of organic matter (OM), assuming that O2 consumption solely was related to heterotrophic activity at the sediment–water interface. Heterogeneity of benthic O2 fluxes denoted changes in time and space of fresh organic material sedimentation. The most labile fraction of exported POC engendered a steep decrease in concentration in the upper 5 mm of vertical O2 profiles. The rupture in the gradient of O2 microprofile may be related to the bioturbation-induced mixing depth of fast-decaying carbon. Average diffusive O2 fluxes showed that this fast-decaying OM flux was much higher than buried POC, although diffusive O2 fluxes underestimated the total sediment oxygen demand, and thus the fast-decaying OM flux to the sediment surface. Sedimentary POC burial was calculated from sediment mass accumulation rate and the organic carbon content measured at the top of the sediment. The proportion of buried POC relative to total exported POC ranged at the most between 50% and 10%, depending on station location. Therefore, for a narrow geographic area like the Bay of Biscay, burial efficiency of POC was variable. A fraction of buried POC consisted of slow-decaying OM that was mineralized within the upper decimetres of sediment through oxic and anoxic processes. This fraction was deduced from the decrease with depth in POC concentration. At sites located below 500 m water depth, where the fast-decaying carbon did not reach the anoxic sediment, the slow-decaying pool may control the O2 penetration depth. Only refractory organic material was fossilized in sedimentary records at locations where labile OM did not reach the anoxic portion of the sediment. 相似文献