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1.
Terry L. Wade Yousra Soliman Stephen T. Sweet Gary A. Wolff Bobby J. Presley 《Deep Sea Research Part II: Topical Studies in Oceanography》2008,55(24-26):2585
The concentrations of polycyclic aromatic hydrocarbons (PAHs) and trace elements were determined for surface (top 2 cm) sediment samples collected during the deep Gulf of Mexico benthos (DGoMB) study .These elements and compounds are known to be toxic to organisms at high concentrations and may affect biological communities. There is no indication of major anthropogenic input of the elements Be, Co, Cr, Fe, Si, Tl, V, K, Mg, Ca, Sr and Zn, based on normalization to Al. The concentrations of these metals in the sediment are a function of the relative amounts of trace-metal-rich Mississippi River-derived silicate material and trace-metal-poor plankton-derived carbonate. This is not true for the elements Ba, Ni, Pb, Cd, As, Cu and Mn, whose concentrations show considerable scatter when normalized to Al and a general enrichment. On a normalized basis, Mn is enriched 5–10 fold, Cu and Ni 2–3 fold and Pb 2 fold over Mississippi River-derived material. These enrichments are likely the result of remobilization of metals from depths in the sediment column where reducing conditions exist. The Ba concentrations at selected sites are higher than those of average clay-rich sediments, but are typical of sediments from near oil well platforms in the northern Gulf of Mexico. In the case of Ba, it seems likely that the enrichments, as high as a factor of 10, are due to disposal of oil well drilling mud. The Ba-enriched samples are from the three shallowest water sites in the Mississippi Trough (sites MT1, 2 and 3) and from site C1 and WC5. All are in an area of intense petroleum exploration and development. PAH concentrations are also elevated at MT1, MT3 and C1. The total PAH concentration ranged from not detected (ND) to 1033 ng/g with a mean of 140 ng/g. Even at the sites most enriched in PAHs and trace elements, the concentrations are not at the levels expected to adversely affect the biota. However, these predicted non-effects are based on research using mostly near-shore estuarine species, not on the indigenous species at the sampling sites. 相似文献
2.
The major and minor element compositions of a suite of abyssal sea-floor ferromanganese nodules and associated sediments from the eastern central Pacific have been used to examine inter-element relationships and the mineralogy of the nodules, the relationship between the composition of nodules and their associated sediments and regional variations in composition with respect to likely modes of formation of such deposits. Apart from Mn and Fe, significant proportions of the total Ti, Ca, Mg, K, Ba, Sr, Th and Y and almost all the P, As, Ce, Co, Cu, Mo, Ni, Pb, Zn and Zr are present in the oxide fractions of the nodules. The Mg, Ba, Cu, Mo, Ni and Zn contents are significantly correlated with the Mn content, while Ti, P, As, Pb, Sr, Y and Zr are similarly correlated with the total Fe content.Nodules from the northeastern tropical Pacific have Mn/Fe ratios higher than those in the oxide fractions of their associated sediments, todorokite as the principal Mn phase and relatively high concentrations of minor elements associated with Mn. Nodules from the south central Pacific have Mn/Fe ratios similar to those in the oxide fractions of the associated sediments, δ-MnO2 as the only Mn-phase, and relatively high concentrations of minor elements associated with Fe. There appears to be a smooth gradation in composition in the tropical Pacific between these two end members.The regional compositional variation is interpreted as a reflection of different sources of metals for, and different growth mechanisms of, sea-floor nodules. The oxide precipitate from sea water consists of δ-MnO2, has a relatively low Mn/Fe ratio and minor element contents related to the total Fe and Mn(δ-MnO2) content. The oxide precipitate forming in areas of very low sedimentation as a result of diagenetic remobilisation in the surface sediment consists of todorokite, and has a high Mn/Fe ratio and enhanced metal content in the Mn-(todorokite)phase. Available information on the morphology and compositional variation of individual nodules from the tropical Pacific corroborates these contrasting metal sources and suggests that they can be resolved on the scale of an individual oxide concretion. 相似文献
3.
In 1984, on a transect covering the whole Baltic Sea and parts of the adjacent North Sea, 160 water samples were taken and analysed for their concentrations of particulate and dissolved metals. In addition, the suspended materials were investigated for their elemental bulk composition.The particulate fractions represented from about 5% (Cd, Cu and Ni) to 50% (Fe and Pb) of the total (particulate plus dissolved) concentrations. For some elements (Ba, Cd, Cu, Pb and Zn), the particulate matter from the surface microlayer was enriched with respect to those suspended materials taken from 0.2 m depth. This could reflect the atmospheric input of metal-rich aerosols. In anoxic deep waters, maximum contents of Zn (6400 μg g−1), Cu (1330 μg g−1) and Cd (12 μg g−1) were observed in the particulate matter, indicating sulphidic forms. On the other hand, under oxic conditions the distribution coefficients (Kd) decreased with the water depth (Cd, Fe and Pb).Relative to global background levels, the particulate matter contained metal “excesses” amounting to more than 90% of the total contents (Cd, Mn, Pb and Zn). Automated electron probe X-ray microanalysis (EPXMA) revealed that the elemental composition of sediments is mainly governed by post-depositional processes of early diagenesis and is only weakly related to the composition of suspended matter in the overlying water body. For instance, in relation to surface mud sediments of the central Baltic net-sedimentation basins, Zn, Cd, Cu and Mn had 30–100% higher levels in the suspended materials. The general pattern of metal contents of particulate matter taken from 10 m depth on a transect between the Bothnian Bay and the North Sea were—possibly as a result of anthropogenic inputs—rather similar for Pb, Zn and Cu. For Fe and Mn, the distribution patterns along the transect were probably governed by the natural loading characteristics and by the biogeochemistry of those elements. 相似文献
4.
东海陆架晚第四纪沉积物化学成分及物源示踪 总被引：11，自引：0，他引：11
东海陆架EA1孔和EA5孔沉积物化学成分变化范围较大。与东海陆架表层沉积物相比，钻孔沉积物的Si,Al,Mg,Mn,Ti,P,Ba,Zr,Co,Ni,Cu,Zn,Cr明显偏高，而Fe,Na,Ca,Sr,Li,U明显偏低，与全球大陆地壳化学组成相比，钻孔沉积物的Si,Li,Rb,Ba,Th,Zr,Hf,Cu,Zn,Pb偏高，而Al,Na,Ca,Mg,Fe,Mn,Ti,P,Sr,U,Co,Ni,V,Cr偏低，钻孔沉积物的化学成分在垂向上具有明显变化，主要受岩性和沉积环境的控制，钻孔沉积物中元素的富集因子（EF）均小于10，接近于1，表明钻孔沉积物主要来自大陆地壳，一些元素因分异或外来物质加入而富集，一些元素则因分异带出而亏损，钻孔沉积物源区的DF值判别表明，钻孔沉积物与现代黄河，长江沉积物均有亲缘关系，可能是在末次冰期最盛期，由于气候带南移，干旱区域扩大，在古长江搬运沉积物中类似现今黄河沉积物的干旱组分明显增加，从而导致了地球化学示踪结果的长江与黄河双重性，或者说古气候的变化导致了古长江搬运物质成分的变化。 相似文献
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7.
台湾海峡大气微量金属的化学特征及其入海通量 总被引：1，自引：1，他引：0
2006～2007年，利用大容量气溶胶采样器在台湾海峡采集79个大气气溶胶样品．采用ICP—MS分析法测定了样品中Pb、Cu、Cd、V、Zn、Fe和Al等金属元素的含量．分析结果显示，台湾海峡大气微量金属含量呈现出明显的季节变化，对大部分元素而言，含量最低值出现在夏季，而最高值出现在冬季，气溶胶中微量金属的含量变化与海峡的气象条件等因素有关．通过富集因子、相关性分析和因子分析，对微量金属的来源进行了判别．台湾海峡大气微量金属的来源特征为：Cu、Pb、Cd、V主要来自污染源，而Al、Fe、Zn则主要来自地壳源．比较和分析了台湾海峡海域微量金属的大气与河流输入，Cu和Zn的大气输入低于九龙江和闽江的输入，而Pb、Cd的大气输入则超过了这2条河流的输入． 相似文献
8.
Atomic absorption spectroscopy (flame and graphite furnace techniques) and instrumental neutron activation analysis were used
for determining the Fe, Mn, Zn, Cu, Pb, Cd, Ag, Co, Cr, As, Se, Sb, Ba, Au, and Hg contents in 25 samples of different tissues
and whole organisms inhabiting the southern trough in the Guaymas Basin (Gulf of California) and in several samples of its
bottom waters. It is shown that the habitat environment of this hydrothermal field with high primary production of both photosynthetic
and bacterial chemosynthetic origin influences the Fe and Mn ratios in the waters of the microbiotopes and the distribution
patterns of the metals in the external and internal organs of the benthic animals. In the dominant specialized taxa, the maximal
bioaccumulation of metals is registered both in the organs related to bacterial chemosynthesis such as the trophosome of Vestimentifera
Riftia pachyptila and the gills of the vesicomyid clam Archivestica gigas and in other organs. The other organisms such as the mollusks Nuculana grasslei, actinias Paraphelliactis pabista, Actinaria, and Spongia and the crabs Munidopsis alvisca demonstrate high bioaccumulation properties as well. The metal concentration coefficient is highly variable ranging from
10 to 104. The changes in the molar Fe/Mn ratio values imply the partitioning of these two metals in the following migration succession:
microbiotope water-external organs-internal organs. 相似文献
9.
Abigail Parcasio Cid Syouhei Urushihara Tomoharu Minami Kazuhiro Norisuye Yoshiki Sohrin 《Journal of Oceanography》2011,67(6):747-764
The distribution of Al, Mn, Fe, Co, Ni, Cu, Zn, Cd, and Pb in seawater was investigated on the Bering Sea shelf (56–64°N,
165–169°W) in September 2000. The unfiltered and filtered seawater samples were used for determination of total dissolvable
(TD) and dissolved (D) metals (M), respectively. The TD-M concentrations were generally higher than in the Pacific Ocean.
TD-Cd was highest in deep water of the outer shelf domain and dominated by dissolved species. The other TD-M were highest
at stations close to the Yukon River delta and had higher fractions of labile particulate (LP) species that were obtained
as the difference between TD-M and D-M. Dissolved Al, Ni, and Cu were characterized by input from the Yukon River. Dissolved
Mn and Co showed maximums on the bottom of the coastal domain, suggesting influence of sedimentary Mn reduction. The correlations
of D-Zn, D-Cd, and macronutrients indicated their distributions were largely controlled through uptake by microorganisms and
remineralization from settling particles. All these three processes (river input, sedimentary reduction, and biogeochemical
cycle) had an influence on the distribution of D-Fe. D-Pb was fairly uniformly distributed in the study area. The stoichiometry
of D-M in the Bering Sea shelf showed enrichment of Co and Pb and depletion of Ni, Cu, Zn, and Cd compared with that in the
North Pacific. The LP-M/LP-Al ratio revealed significant enrichment of the other eight metals relative to their crustal abundance,
suggesting importance of formation of Fe–Mn oxides and adsorption of trace metals on the oxides. 相似文献
10.
黄河口海区沉积物柱样中碳酸盐组分 总被引：5，自引：1，他引：5
于１９８９年５月在黄河口海区采集４个沉积物柱状样,以原子吸收法测定其碳酸盐组分中Ｃａ,Ｍｇ,Ｆｅ,Ｎａ,Ｍｎ元素的含量。结果表明,含量分布基本遵循“元素粒度控制律”,即沉积物粒度细时,元素含量超于富集。结果还证明,受黄河水影响越大,沉积物碳酸盐Ｍｎ／Ｆｅ比值越高,可以以此判断沉积物受黄河水影响的程度;ＣａＣＯ３含量亦存在类似现象。相关分析表明,碳酸盐组分中Ｍｎ含量与ＣａＣＯ３含量相关较好,而Ｆｅ与 相似文献
11.
《Marine Geology》2001,172(1-2):147-165
This study aims at apprehending the major forcing factors which govern the spatial and vertical Mn and Fe distributions in ten cores from the Gulf of Lions. Speciation by chemical leaching experiments helps understanding their chemical behaviour during the early diagenetic processes in a marine environment under strong continental influence.The distribution and chemical behaviour of Mn and Fe differ drastically. The strong dependence of Mn distribution on chemical conditions is expressed by a marked solid phase Mn enrichment in the oxic layers of sediment deposits. This enrichment increases with decreasing sedimentation rate (increasing water depth). It is illustrated by an enhanced portion of total Mn in the reducible phase and the precipitation of todorokite on calcareous supports in the upper part of the deepest cores. As a result, 65% of the margin total particulate Mn is thought to be stored in slope deposits in a relatively strongly held association. Conversely, the low chemical mobility of iron in the sedimentary column is indicated by uniform depth profiles and an exclusive location in the residual chemical phase in all the studied sites. The Fe distribution is largely controlled by the dispersion of particulate material on the margin from the Rhône River main source.A budget of Mn and Fe accumulation based on the average amount of total Mn and Fe content of sediments deposited during the last 100 yr, has been made taking into account diagenetic readjustments. The total Mn and Fe amount stored on the margin during the last century is estimated to be 1.5×106 and 54×106 t, respectively. These values are seven times higher than the total secular external inputs calculated on the basis of present day riverine and atmospheric fluxes. This large discrepancy is mainly explained by the sharp decrease of the Rhone River discharge after dam buildings between 1950 and 1958. A residual discrepancy dating before 1950, is likely to be due to seafloor erosion and gravity induced mechanisms. 相似文献
12.
The present study was undertaken for assessing the level of heavy metals such as iron, manganese, zinc, copper, nickel, cadmium, lead, and cobalt in recent sediment samples of Safaga Bay, Egypt. Concentration of heavy metals in sediments shows significant variability and ranges from 863.37 to 1144.93 ppm for Fe, 64.29–586.8 ppm for Mn, 2.7–12.68 ppm for Zn, 3.01–7.2 ppm for Pb, 1.53–3.29 ppm for Ni, 0.55–1.57 ppm for Co, 0.16–1.37 ppm for Cu, and 0.22–0.4 ppm for Cd. Sediment pollution assessments were carried out using an enrichment factor and geoaccumulation index. The calculation of enrichment factor showed that Cd is enriched by 4.1 due to phosphate sources in Safaga Bay. The Geoaccumulation index results revealed that there are positive and negative correlations between Fe, Zn, Mn, Pb, Ni, Cu, Co, and Cd indicating that these metals have complicated geochemical behaviors. 相似文献
13.
D. J. Mackey J. E. O'Sullivan R. J. Watson G. Dal Pont 《Deep Sea Research Part I: Oceanographic Research Papers》2002,49(12)
Profiles of total dissolvable Cd, Cu, Mn and Ni are reported for samples collected from the southwest Pacific in 1989, from the western equatorial Pacific along 155°E at 5°S, 0° and 5°N in 1990 and 1993, and along the equator from 143°E to 152°E and in the Bismarck Sea in 1997 and 2000. Profiles of Cd along 155°E in 1990 and along the equator were essentially the same but, in 1993, Cd values at 5°N were higher by a factor of about 1.5–2 than at 5°S over the depth range 500–1500 m. Similar, but less pronounced, differences were observed for PO4 and Ni. Cd and Ni were both strongly correlated with PO4, and an even stronger correlation was found between Ni and Cd. The concentration of Ni did not fall below ≈2 nmolkg−1, even in the nitrate-depleted waters of the western equatorial Pacific, where primary production is strongly dependent on recycled nitrogen (mainly ammonia and urea). It is proposed that this residual Ni is not bioavailable and that Ni could be biolimiting, since the metabolism of urea requires the nickel-containing enzyme urease. The impact of the Sepik River on Cd, Cu and Ni concentrations was small but elevated concentrations of Mn were observed near the Sepik River and close to the coast suggesting that the rivers and sediments on the north coast of New Guinea are a significant local source of Mn to the Bismarck Sea. Simple mass balance calculations show that the elevated levels of Mn observed in the Equatorial Undercurrent cannot be due to input from the rivers of New Guinea and they were attributed to the trapping of particulate matter due to strong current shear. A strong hydrothermal source of Mn was observed in the central Bismarck Sea. 相似文献
14.
Temperature, pH, total alkalinity, dissolved oxygen, silicate, nitrate, phosphate and the Mn, Fe and Al contents of suspended particulate matter (SPM) were measured in the Rimouski River estuary as functions of chlorinity during the period May—September 1980.At any given time, total alkalinity (TA) is conservative within the estuary with respect to chlorinity. However, the total alkalinity (TA) of the freshwater is related to river flow. This is attributed to dilution of the river water with bicarbonate-poor rainwater.Generally, pH follows the same pattern observed for TA in freshwater. Dissolved oxygen is usually more concentrated in freshwater and decreases linearly with increasing chlorinity. Freshwater is always saturated or supersaturated with respect to O2. Seasonal fluctuations are attributed to temperature variations.There is no evidence for removal of soluble silicate from the freshwater entering the sea. The concentration of silicate in the freshwater is strongly influenced by rainfall. Soil leaching, conditioned by high rainfall increases the concentration of soluble silicate in freshwater. Nitrate behaves similarly whereas phosphate is complicated by the presence of sewage.Analysis of the Mn, Fe and Al contained in the SPM indicates dilution of river-borne particles rich in Mn by others less rich in this element. A decrease in Mn content with increasing chlorinity and SPM concentration as well as increasing concentrations of SPM with increasing chlorinity indicate that the composition is controlled primarily by physical mixing of material from two sources rather than by chemical processes. Within the analytical precision the Fe/Al ratio does not vary with the chlorinity. 相似文献
15.
红树植物红海榄叶化学组成研究 总被引：4，自引：0，他引：4
对红树植物红海榄叶的基本化学成分水分,灰分,灰分中酸不溶物,灰分中S(SO42-),粗蛋白,粗脂肪等及氨基酸和微量元素的组成和含量进行了系统的分析测定。其基本化学组成各成分含量分别为:水分(69.18%),灰分(3.04%),灰分中酸不溶物(0.094%),灰分中S(SO42-)(0.052%),粗脂肪(7.75%),粗蛋白(7.14%);测得了红海榄叶中17种氨基酸,其总含量为10.7mg/g,其中人体必须氨基酸有7种,占所含氨基酸总量约26%;采用全谱直读等离子体原子发射光谱仪对红海榄叶进行了31种微量元素的分析测定,测得了其中18种元素的含量,红海榄叶中含有丰富的人体必须的矿物质元素。 相似文献
16.
邻近城市土壤重金属对九龙江口沉积土壤的影响 总被引：2，自引：0，他引：2
在研究建立于漳州地区生态地球化学调查基础上,对河口湾沉积物的重金属与人口高度集中的城市地区土壤重金属的分布特征进行了对比,分析了人为活动对河口的影响,结果表明,城区与河口湾表层样品都舍有相对区域基准值较高的Hg、Cd,而且Hg富集系数要远高于Cd的富集系数。分析两种元素来源与迁移方式可知,Hg由于可通过气态形式迁移而对河口影响更大。城区与河口湾样品的重金属进行聚类分析与主因子分析结果表明：城区土壤的As、Zn、Mo、Ni、Cr和Mn主要来自基岩来源。Pb、Se、Cd可以作为人为污染的指示元素,Hg、Sn显示与其他元素具有相对独立的行为。河口湾的元素组合与城区重金属基本相似,但Pb、Cu、Se、Mo、Cd显示出两种因素都有较大影响,可以指示人为影响与基岩源的双重作用。 相似文献
17.
海水养殖池沉积物中重金属形态和生物酶活性的关系研究 总被引：1，自引：0，他引：1
以连云港市对虾养殖池表层沉积物为研究对象,采用Tessier连续萃取法,研究了表层沉积物中重金属(Cu、Zn、Pb、Cd、Cr、As、Mn)的赋存形态和酶(脲酶、碱性磷酸酶、过氧化氢酶、转化酶)活性的相关性。结果表明,重金属Cu和Zn以有机-硫化物结合态为主要的赋存形态,Pb以铁锰氧化物态为主要的赋存形态,Cd以可交换态(平均33.47%)和碳酸盐结合态(平均31.16%)为主要存在形态,Cr和As主要以残渣态存在,Mn的铁锰氧化物态比例最高。脲酶的活性范围为0.45—8.96mg/(g·24h),碱性磷酸酶活性范围为2.45—6.69mg/(g·24h),过氧化氢酶活性范围为0.14—2.36m L/(g·min),转化酶活性范围为0.45—10.45mg/(g·24h)。脲酶活性与Cd、As的可交换态、Cd的碳酸盐结合态、Cu、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态之间显著相关;碱性磷酸酶活性与Zn、Cd的铁锰氧化物态显著相关;过氧化氢酶活性与Cd的可交换态、碳酸盐结合态及残渣态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫结合态之间显著相关;转化酶活性与Cu、Cd、As的可交换态、Cd的碳酸盐结合态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态、Cd、As的残渣态之间显著相关。酶活性可以用来指示海水养殖池沉积物中重金属的形态转化过程。 相似文献
18.
A total of 150 samples were collected at a 10-days' anchor station in the Bornholm basin (55° 31.1′N, 15° 32.1′E) and analyzed for dissolved (< 0.4 μm) and particulate trace metals. For dissolved Mn, large gradients have been found in the vertical distribution with minimum concentrations (< 0.2 μgl?1) in the halocline zone and considerably higher values in the deep waters (up to 50 μgl?1). Ultrafiltration studies indicate that dissolved Mn is probably present as Mn2+ in the oxygenated bottom layer. The primary production process was not evident in the particulate Mn profile; the suspended particulate material (SPM), however, shows a considerable enrichment with depth, apparently due to Mn-oxide precipitation.The distribution of dissolved Fe was rather homogeneous, with average concentrations throughout the water column between 0.86 and 1.1 μgl?1, indicating that the oxidation of Fe2+ ions released from the sediments must already be complete in the very near oxidation boundary layer. Relatively high concentrations of particulate Fe were actually measured in the bottom layer, with the maximum mean of 11.2 μgl?1 at 72 m. Similarly to Mn, the profile of particulate Fe does not reflect the SPM curve of the eutrophic layer. On average, about 70% of the total Fe in surface waters was found to be particulate.The average concentrations of dissolved Zn, Cd and Cu were found to be rather homogeneous in the water column but showed a relatively high variability with time. A simplified model on trace-metal uptake by phytoplankton indicates no significant change in dissolved metal concentrations during the period of investigation. On average, only 1.7% Zn, 3.3% Cd and 9.8% Cu of the total metal concentrations were found in particulate form. SPM analyses showed significant correlations of Zn, Cd and Cu with Fe, indicating that particulate iron is an important carrier for particulate trace metals in Baltic waters. 相似文献
19.
南海铁锰结核(壳)的元素地球化学研究 总被引：1，自引：0，他引：1
本文利用南海11个铁锰结核(壳)样品的化学分析资料,研究了铁锰结核(壳)中Fe,Mn,Cu,Co,Ni,Pb,Zn,Cr,K,Na,Ca,Mg,Si,P,Al,Ti,Sr,Ba及∑REE的元素地球化学特征。结果表明:(1)铁锰结核(壳)以高Fe,∑REE,低Mn,Cu,Co,Ni等元素为主要特征;(2)铁锰结核(壳)中Fe,Mn间无明显相关,而Fe与∑REE,∑Ce,∑Y呈弱的正相关,Mn与∑REE,∑Ce,∑Y呈明显的正相关,结壳中Fe,Mn与Si,Al,Cu Co Ni呈负相关;(3)结核(壳)中Mn/Fe与Cu/Ni,Ce/La呈负相关,Mn/Fe主要受Mn控制;(4)结核(壳)中Fe,∑REE等元素主要来自南海陆源中酸性岩类的风化、淋滤和沉积。 相似文献
20.
Suspended matter was collected at 30 stations in the Baltic and Kattegatt, at the thermocline and at the bottom, and analysed for Na, Ca, Mg, Si, Ti, Al, Fe, Mn, Ba, Sr, Ni and V. The composition of the suspended matter varies considerably, but can be described as a mixture of: (1) 12–25% terrigenous detritus with much Si, Al, Ti and Fe; (2) 75–88% biological matter with much Ni, V and Ba; and (3) some Mn-oxyhydroxide.The annual efflux of water from the Baltic is about 460 km3, with a suspended load in the Baltic straits of ～1.2–3.6 mg ash material l?1 These values imply that much Si, Ti, Al, Fe, Sr, Ni and V and particularly much Ba and Mn are lost from the Baltic in the suspended load.The average suspended matter is richer in Mn(5×), Ba(2.5×), Sr(4×) and V(1.8×) than permanently depositing Baltic sediments. These constituents are relatively enriched in pelagic deposits, i.e. it is likely that much Mn, Ba and V in deep-sea sediments derive from the continents via suspended transport. This conclusion is supported by the similarity between suspended matter and average Atlantic pelagic sediment. 相似文献