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1.
The geochemical study of 5 sediment cores obtained from different shallow hydrothermal fields along the volcanic arc (Methana, Milos, Kos and Yali), revealed that the degree of rock hydrothermal alteration from one area to another is different and is influenced by the physical and geochemical properties of the hydrothermal venting fluids and the type of the rocks in the substrate. The submarine hydrothermal fields in the central Aegean Sea are linked with the Hellenic Volcanic Arc and imprint their hydrothermal influence on the local marine sediments. Hydrothermal venting fluids differ in pH, temperature, gas and metallic element content, intensity of gas and water flux, while rock substrate is variable in terms of thickness and chemistry of the marine sediments and the mineral deposits. The analytical results showed that the lowest values of Fe are observed in Palaeochori Bay (0.72%) and the highest values are found in Bros Thermi (2.72%). The highest Mn concentrations are found in Bros Thermi (407 ppm) and the lowest are found in Yali (29 ppm). Cu and Pb highest concentrations are found in Bros Thermi (21 ppm) and Thiafi Bay (16 ppm), and the lowest in Yali (1 ppm). Zn highest values are found in Bros Thermi (56 ppm) and the lowest values in Kephalos Bay (10 ppm). Finally, the Ca and Mg-richest layers are observed in Kephalos 7.5 and 0.98% respectively and the lowest are observed in Milos (0.01% for Ca) and Yali (0.12% for Mg). The hydrothermal activity presented variations with geological time and hydrothermal suspended particulate matter coming out from the vent outlets also influence the sediment geochemistry. As an example in Methana, high concentrations of Cu and Zn in SPM result in high levels of Cu and Zn in the sediments.  相似文献   

2.
The REE (rare-earth) contents of sixty-three <2 μ fractions of Pennsylvanian and Permian platform sediment from the mid-continent of the U.S.A. vary considerably (ΣREE = 46–439 ppm;La/ Lu = 5.2–15.7; correlation coefficient of REE with La/Lu = 0.89), but the Eu/Sm ratios are nearly constant even in reducing environments that concentrate U (0.16–0.22). There is no correlation of REE content to clay mineralogy.Lower Permian <2 μ fractions from continental to nearshore marine sediment in Oklahoma have higher REE content (244–261 ppm) than marine facies in Kansas (46–140ppm), but <2μ Upper Permian fractions in an evaporite basin have constant but high REE content (288–281 ppm; one = 153—ppm). All Pennsylvanian <2 μ fractions from Oklahoma have high REE content (209–439 ppm), and fractions from Kansas cyclothems have variable REE content (86–438 ppm). REE content in the <2 μ fractions is inherited from the provenance, but is modified by ion exchange during weathering, transportation, or deposition. Exchangable REE tend to be concentrated in clay minerals in basic environments, but removed in acid environments.Sand and gravel-size fractions consist mostly of quartz or chert so their REE content is low (7.9–40.6 ppm) although heavy minerals may contribute a large fraction of the REE content. Unexpectedly, silt-size fractions have REE contents (74–355 ppm) that are usually lower but similar to their <2 μ fractions, and the REE contents do not correlate to clay mineral/quartz ratios. The interpretation of REE content in sedimentary rocks needs to be done cautiously due to the above factors.  相似文献   

3.
A mine-tailings spill occurred on the island of Marinduque, Philippines, on 24 March 1996. Originating from the Marcopper Mine, tailings sludge flowed down the Boac River abruptly and during subsequent storm events. Most of the tailings material has since accumulated in the nearshore environment along the western coast of the island. Nineteen sediment cores were collected from this site and analyzed for heavy metals. Elevated concentrations of Cu (706-3,080 ppm), Mn (445-1,060 ppm), Pb (43-56 ppm), and Zn (131-276 ppm) are present in the tailings. Two horizons of high metal concentrations in the marine sediment profile are interpreted to correspond to two distinct tailings input events. The lower horizon corresponds to the original 1996 spill, whereas the spike near the surface is thought to be a combination of input due to dredging of the river in 1997 and reworking of sediments. A previous history of contamination is also deduced from the metal profiles. The volume of tailings material released into the marine environment due to the spill is estimated to be 180,000 to 260,000 m3.  相似文献   

4.
Lack of high-spatial-resolution soil and sediment arsenic data for Hawai‘i has generated substantial disagreement between researchers and regulators regarding the magnitude of natural levels of arsenic in Hawai‘i and rendered difficult the defining of areas of anthropogenically elevated arsenic. Our earlier research into the occurrence of arsenic in terrestrial and marine environments revealed widely disparate concentrations of arsenic with no apparent spatial pattern. To better understand the distribution and abundance of arsenic in soils and sediments of O‘ahu, we collected an additional 64 samples at locations chosen to represent different environments with varying degrees of human impact. We found surface arsenic values that ranged from 0.28 to 740 ppm with a median concentration of 8.1 ppm, which is above the global median of 5 ppm and US soil median of 5.2 ppm. Higher concentrations of arsenic (up to 913 ppm) were encountered at depth in soil cores. The median arsenic in streambed sediments from one of our earlier studies of 6.1 ppm was comparable to the conterminous US median of 6.3 ppm; however, we encountered arsenic concentrations as high as 43.9 ppm (median = 8.60 ppm, n = 75) in marine sediments in recent work off the leeward coast of O‘ahu. Overall, arsenic in the soils and sediments of O‘ahu is elevated relative to world and national values, but there still is no readily discernible pattern in the distribution of arsenic to explain these elevated values.  相似文献   

5.
Atomic emission spectrographic analysis of the trace inorganic constituents of marine humic substances gave the following range of concentrations: Si, 200 ppm to > 2%; Al, 400 ppm to ~ 1%; Fe, 600–3000 ppm; Ca, 600 ppm to > 2%; Mg, 20–6000 ppm; Na, 600 ppm to > 2%; Ag, < 6–600 ppm; B, < 60–1000 ppm; Cu, 600–4000 ppm; Mn, 8–100 ppm; Mo, <20–3000 ppm; Ni, 100–1000 ppm; Pb, < 40–600 ppm; Sn, 40–600 ppm; Ti, < 20–2500 ppm; V, 20–200 ppm; Zn, 350–4500 ppm; Zr, < 60–500 ppm.Humic substances contain a sizeable portion of the Cu, Mo and Zn found in sediments, but are less important for Ni, Co and Pb, and are insignificant for the Mn, V and Fe content. The metals are mostly introduced into the humates during their diagenetic formation in sediment by dissolution of metals from various mineralogical phases. A precursor of the sedimentary humates, the polymeric organic material dissolved in interstitial water, contains most of the Cu and Zn, about half of the Ni, Fe and Co, and very little of the Mn found in interstitial water. Comparison of the data on humates with that obtained by H2O2 treatment of sediments indicates that Cu, Zn and possibly most of the Mo are associated with organic matter, but that Ni and Co are associated with sulfides.  相似文献   

6.
Possible sources of gallium in hydrothermal-sedimentary ferromanganese crusts of the Belyaevsky Seamount (Central Basin, Sea of Japan) are considered. Studies with successive selective leaching have shown that ~ 80% of Ga are present in the manganese fraction. The Changbaishan Volcano ash with up to 35.3 ppm Ga has been found in the marine sediment column located in the immediate vicinity of the Belyaevsky Seamount. This suggests that Ga of the Fe–Mn crusts of the seamount was supplied with the ash of volcanic rocks containing up to 300 ppm Ga.  相似文献   

7.
海洋沉积物中的动物多样性及其生态系统功能   总被引：7，自引：0，他引：7  
海洋沉积物中的动物群是海洋生态系统中的重要组成部分,其多样性对地球生命支持系统至关重要。从海洋沉积物生境、沉积物中的动物类群、个体大小、食性、生态系统功能等方面探讨了海洋沉积物中的动物多样性现状,讨论了沉积物动物多样性在生态系统过程中的重要作用。海洋沉积物环境多种多样,为沉积物动物多样性提供了基础。在海洋沉积物中,动物的类群繁多、物种多样性极高,不仅形态差别很大,食性丰富多样,而且分化出多种多样的功能群。海洋沉积物动物群参与全球物质的循环和污染物的代谢、转化、迁移,在生态系统能流过程及沉积物移动和稳定性方面也起着重要的作用。最后,提出了研究和保护海洋沉积物动物多样性的若干建议。  相似文献   

8.
Arsenic (As) concentrations as high as 179 μg/L have been observed in shallow groundwater in the Alberta’s Southern Oil Sand Regions. The geology of this area of Alberta includes a thick cover (up to 200 m) of unconsolidated glacial deposits, with a number of regional interglacial sand and gravel aquifers, underlain by marine shale. Arsenic concentrations observed in 216 unconsolidated sediment samples ranged from 1 and 17 ppm. A survey of over 800 water wells sampled for As in the area found that 50% of the wells contained As concentrations exceeding drinking water guidelines of 10 μg/L. Higher As concentrations in groundwater were associated with reducing conditions. Measurements of As speciation from 175 groundwater samples indicate that As(III) was the dominant species in 74% of the wells. Speciation model calculations showed that the majority of groundwater samples were undersaturated with respect to ferrihydrite, suggesting that reductive dissolution of Fe-oxyhydroxides may be the source of some As in groundwater. Detailed mineralogical characterization of sediment samples collected from two formations revealed the presence of fresh framboidal pyrite in the deeper unoxidized sediments. Electron microprobe analysis employing wavelength dispersive spectrometry indicated that the framboidal pyrite had variable As content with an average As concentration of 530 ppm, reaching up to 1840 ppm. In contrast, the oxidized sediments did not contain framboidal pyrite, but exhibited spheroidal Fe-oxyhydroxide grains with elevated As concentrations. The habit and composition suggest that these Fe-oxyhydroxide grains in the oxidized sediment were an alteration product of former framboidal pyrite grains. X-ray absorption near edge spectroscopy (XANES) indicated that the oxidized sediments are dominated by As(V) species having spectral features similar to those of goethite or ferrihydrite with adsorbed As, suggesting that Fe-oxyhydroxides are the dominant As carriers. XANES spectra collected on unoxidized sediment samples, in contrast, indicated the presence of a reduced As species (As(−I)) characteristic of arsenopyrite and arsenian pyrite. The results of the mineralogical analyses indicate that the oxidation of framboidal pyrite during weathering may be the source of As released to shallow aquifers in this region.  相似文献   

9.
Trace element concentrations in shallow marine sediments of the Buyat-Ratototok district of North Sulawesi, Indonesia, are affected by submarine disposal of industrial gold mine tailings and unregulated dumping of tailings and wastewater from small-scale gold mining using mercury amalgamation. Industrial mine tailings contained 590–690 ppm arsenic, 490–580 ppm antimony, and 0.8–5.8 ppm mercury. Tailings-affected sediment As and Sb concentrations were 20–30 times higher than in muddy sediments not contaminated with tailings, and 50–60 times higher than pre-mining average. Highest mercury concentrations were observed in sediments affected by small-scale mining using mercury amalgamation (5–29 ppm). Concentrations of most other trace elements were comparable in sediments affected by both types of mining and were slightly higher than regional averages for sediments collected before the onset of industrial mining. Elevated concentrations of both As and Sb in approximately equal proportions suggest tailings dispersal of at least 3.5 km. Mercury released from artisanal gold mining dispersed up to 4 km from river mouths. Slight increases in concentrations of non-mercury trace elements in areas affected by artisanal mining over pre-industrial mining concentrations were probably caused by increased rates of erosion. Electronic supplementary material Supplementary material is available in the online version of this article at and is accessible for authorized users.  相似文献   

10.
Growth zones and individual sublayers from one manganese nodule and three manganese crusts from an area south of Hawaii were analysed for U and Th by the delayed-neutron counting technique.The concentrations of uranium and thorium in the manganese nodule are highest in the outermost zone on top of the nodule, being the surface last exposed to sea water. In this zone U varies from 6.3 to a maximum of 8.3 ppm in different sublayers, decreasing to 5.0 ppm in the inner zones and 3.4 ppm in the outer zone last exposed to the sediment. Ferromanganese material scraped from the zone last exposed to the sediment which has low concentrations of Fe, relative to the zone last exposed to sea water, has also low U contents (2.7 ppm).Th concentrations are higher in the outermost zone on top of the nodule (40 to a maximum of 130 ppm) than in the zone last exposed to the sediment (about 20 ppm Th).Manganese crusts contain up to 9 ppm U in the outermost zones last exposed to the sea water. They also have higher concentrations of Th (up to 64 ppm) relative to the inner zones of the crust growing on altered andesitic rock, which contains about 8 ppm U and about 26 ppm Th as an average.  相似文献   

11.
The 10B(n, α)7Li nuclear reaction has been used with alpha-sensitive plastic track detectors to determine boron concentrations in siliceous live-collected and fossil sponge spicules. This radiographic technique allows B determinations with 5–6% uncertainties on objects 20–25 μm in diameter and for concentrations as low as 0.5 ppm. Boron concentrations in spicules from different specimens from the same location agreed to within 10% when the spicules were not: (1) smaller than 20 μm in diameter, (2) from dictyonine skeletons, (3) the extremely large root-like spicules found in some soft substrate hexactinellids, or (4) microscleres. These criteria also applied to spicules found in sediment samples. Spicules from live-collected sponges exhibited a taxonomy-independent correlation of B concentrations with water salinity for samples from regions of low water temperature and high productivity. Measured concentrations ranged from nearly 0 ppm B (freshwater sponges) to 500–700 ppm (marine sponges), with intermediate values for brackish-water specimens. However, spicules from tropical, low-productivity marine locations contained markedly less boron than spicules from temperate, high-productivity regions. Thus, water temperature and/or food supply also seem to influence B concentrations. Pleistocene spicules from deep-sea cores contained less boron than was expected in comparison with live-collected spicules based on present water temperatures and nutrient supplies, but B concentrations did not vary with depth in the cores. Infrared spectroscopy, electron microprobe analysis and visual inspection revealed no evidence for chemical or mineralogic alteration. It is not clear whether the lower B concentrations of the Pleistocene samples are the result of diagenetic processes or the as yet undefined effects of differences in food supply and/or environmental conditions.  相似文献   

12.
介绍了潮间带地区,海潮引起海水位变动时,一种原位测定海底沉积物渗透系数的新方法.该方法不仅可以测定海底沉积物水平和垂向的渗透系数,还可对海底沉积物中任意倾斜方向的渗透系数给予测定,这一点是传统测定沉积物渗透系数的方法所无法达到的.通过所测数据,我们可以画出表征含水层渗透系数的椭圆,从而确定海底沉积物各相异性的性质,这一结果对于研究地下水流动、河水泄流及海底沉积物中污染物的运移意义十分重大.该方法能有效的用于不同海洋地质情况,并且相比颗粒分析、渗透仪、和抽水试验等其他方法更经济,更实用.  相似文献   

13.
The Gol-e-Zard Zn-Pb deposit is one of several sediment-hosted Zn-Pb deposits found in the central part of the Sanadaj-Sirjan Zone, known as the Isfahan-Malayer belt, western Iran. Mineralization occurs in Upper Triassic to Jurassic phyllites and meta-sandstones. Sphalerite and galena are the most abundant metallic ores, with minor chalcopyrite. Calcite and quartz are the main gangue minerals. Fissure filling, replacement textures and especially mineralized faults, suggest an epigenetic stage in the Gol-e-Zard deposit formation. Geochemical studies of mineralized rocks show high concentrations of Zn, Pb and Cu,（Zn and Pb 〉 10000 ppm and Cu average 3000 ppm）. LREE enrichment（LREE〉HREE, La/Lu average 1.44） and positive Eu anomalies（Eu/Eu＊〉1 average 1.67） indicate reducing conditions during the deposition of deposit. However, some samples do not display negative Ce anomalies, which indicate that localized oxidizing conditions are also present. This study indicates that the Gol-e-Zard deposit formed due to circulating hydrothermal fluids in a marine environment. A SEDEX-type genesis, which is defined by circulating hydrothermal fluids through sediments in a marine environment, and syngenetic precipitation of Zn and Pb sulphides, is suggested for the Gol-e-Zard deposit. Emplacement of some granitoid intrusions such as the Aligudarz granitoid intrusion remobilized mineralizing fluids and metamorphosed the Gol-e-Zard deposit.  相似文献   

14.
Trace metal concentrations were investigated in a recent sediment core collected from the Rehri Creek area of the Karachi coast,Sindh-Pakistan.The core was sliced horizontally at 2.5-cm intervals to determine grain size,sediment composition,pH,organic matter,and acid-leachable trace metals:cadmium,chromium,copper,lead,and zinc.The trace metals were analyzed by ICP.To separate anthropogenic from geogenic input,several approaches were made,including comparison with sediment quality guidelines—ecotoxicological sense of heavy metal contamination and classification by quantitative indexes.Grain-size analysis and sediment composition of core sample show a sandy nature with neutral pH.Elemental sequence(ES)of the trace metals is in the order of Zn(19.2-109.56 ppm)>Si(66.46-101.71 ppm)>Ba(12.05-26.86 ppm)>As(8.18-17.36 ppm)>Ni(4.2-14.69 ppm)>Cr(3.02-9.62 ppm)>Pb(2.79-6.83 ppm)>Cu(2.2-5.29 ppm)>Co(0.9-2.05 ppm).Thus it is likely that the area may face a serious threat of metal pollution with the present deposition rates unless stringent pollution control norms are adopted.The Sediment Geo-accumulation Index shows that there is no Cr,Cu,Ni,Pb,Zn,or Fe pollution;however,the former index and the Pollution Load Index indicate arsenic pollution in the sediments.  相似文献   

15.
Through a large-scale examination of the morpho-sedimentary features on sea floors in the Taiwan–Luzon convergent margin, we determined the main sediment dispersal system which stretches from 23°N to 20°N and displays as an aligned linear sediment pathway, consisting of the Penghu Canyon, the deep-sea Penghu Channel and northern Manila Trench. The seafloor of South China Sea north of 21°N are underlain by a triangle-shaped collision marine basin, resulting from oblique collision between the Luzon Arc and Chinese margin, and are mainly occupied by two juxtaposed slopes, the South China Sea and Kaoping Slopes, and a southward tilting basin axis located along the Penghu Canyon. Two major tributary canyons of the Formosa and Kaoping and small channels and gullies on both slopes join into the axial Penghu Canyon and form a dendritic canyon drainage system in this collision marine basin. The canyon drainage system is characteristic of lateral sediment supply from flank slopes and axial sediment transport down-canyon following the tilting basin axis. The significance of the collision marine basin in term of source to sink is that sediments derived from nearby orogen and continental margins are transported to and accumulated in the collision basin, serving as a temporary sediment sink and major marine transport route along the basin axis. The comparison of the Taiwan–South China Sea collision zone with the Papua New Guinea collision zone of the western Solomon Sea reveals remarkable similarities in tectonic settings and sedimentary processes that have resulted in similar sediment dispersal systems consisting of (1) a canyon drainage network mainly in the collision basin and (2) a longitudinal sediment transport system comprising a linear connection of submarine canyon, deep-sea channel and oceanic trench beyond the collision marine basin.  相似文献   

16.
Hydrocarbon results from gas chromatography of 60 recent sediment and 10 benthic algae samples delineate two distinct shelf environments in the northeastern Gulf of Mexico.Sediments off Florida (shell hashes and sands) have moderate amounts of lipids/total sediment (average 113ppm ± 80%) but low hydrocarbon levels (average 3.06 ppm ± 41%). Aliphatic hydrocarbons are dominated by a series of branched or cyclic, unsaturated C25 isomers. The major n-alkane is n-C17. The n-alkane and isoprenoid patterns are consistent with a marine hydrocarbon source.Sediments closer to the Mississippi River (silts and clays) contain large amounts of lipids (average 232 ppm ± 53%) and hydrocarbons (average 11.7 ppm ± 55%) to total sediment. Aliphatic hydrocarbons are mainly odd carbon number high molecular weight n-alkanes, indicating a terrigenous hydrocarbon source. Isoprenoids are present in greater abundance than in sediments off Florida (n-C17/ pristane and n-C18/phytane ratios ~2to 3). Relatively large amounts of n-C16, together with an even distribution of n-alkanes in the range C14–C20 and a substantial unresolved envelope all point to a fossil fuel input to the Mississippi samples.Samples off the Alabama coast show intermediate characteristics.  相似文献   

17.
研究了海洋沉积物提取液中28种多氯联苯(PCBs)、16种多环芳烃(PAHs)和21种有机氯农药(OCPs)在硅胶-氧化铝复合净化柱上的同时净化与分离效果,结果表明:在充填4 cm3%去活化氧化铝-6 cm 3%去活化硅胶的8 mm i.d×15 cm固相萃取净化柱上,使用10 mL正己烷作为淋洗PCBs的分割点,可实现PCBs、PAHs和OCPs的满意分离,更有利于PCBs与高环数PAHs、极性较强OCPs的分离。继续用20 mL正己烷-二氯甲烷混合液(体积比1∶1)洗脱,28 PCBs、16种PAHs和21种OCPs均可获得有效回收,回收率分别为75%~110%、76%~115%、75%~130%。经海洋沉积物标准参考物质验证,该方法实用、可靠,流程简单,试剂消耗少,成本低,适用于海洋环境地质调查中基质复杂沉积物样品的定量分析。  相似文献   

18.
海洋环境沉积物输运研究进展   总被引：6，自引：0，他引：6  
海洋环境中沉积物的输运涉及复杂的过程和机制。20世纪后半叶发展起来的悬沙输运数学模型已经成为海洋沉积动力学的一个有力的研究工具。悬沙输运数学模型的有效运行需要正确的数值解法和模型中所含参数的确定,包括悬沙沉降速度、扩散系数、底床糙度和切应力,以及底边界上的沉降-再悬浮通量。由于复杂的水动力条件、屏蔽效应以及海底生物扰动等因素的作用,海洋环境推移质输运的经验、半经验公式具有一定的局限性。因此,充分考虑以上各种因素是正确预测海洋环境中推移质输运的关键。海洋环境沉积物输运理论的进一步发展需要着重进行各种过程和机制的研究,而这项工作依赖于高精度、高分辨率现场观测仪器的发展和更先进的颗粒态物质运动理论的建立。  相似文献   

19.
 The marine coastal sediments from Togo have been analysed for the trace elements Cd, Cr, Cu, Ni, Pb, Sr, V, Zn and Zr to ascertain the geo-ecological impact of dumping of phosphorite tailings into the sea. Trace element concentrations ranged from 2–44 ppm for Cd, 22–184 ppm for Cu, 19–281 ppm for Ni, 22–176 ppm for Pb, 179–643 ppm for Sr, 38–329 ppm for V, 60–632 ppm for Zn and 18–8928 ppm for Zr. Regional distribution of trace elements in the marine environment indicates that the concentrations of Cr, Cu, Ni, Pb, V, Sr and Zn increase seawards and along the coastal line outwards of the tailing outfall, whereas Cd and Zr showed reversed spatial patterns. Sorting and transport of phosphorite particles by coastal currents are the main factors controlling the distribution of particle-bound trace metals in the coastal environment. The Cd, Sr and Zn concentrations decrease with decreasing grain size in marine coastal sediments, whereas Cr, Cu, Ni and Zn concentrations increase with decreasing grain size. Percolation and shaking experiments were carried out in laboratory using raw phosphate material and artificial sea water. Enhanced mobilization of Cd from phosphorites by contact with the sea water was observed. Received: 11 May 1998 · Accepted: 20 October 1998  相似文献   

20.
A study has been completed of the baseline concentrations of Mo in bottom sediments of the major rivers in Colorado. Three hundred and seventy-nine samples were taken from 14 rivers in the state. The geometric means for the concentration of Mo in the minus 80-mesh fraction of the sediment were found to vary from 1.2 to 14.0 ppm. The geometric mean for each river can be logically grouped according to the presence or absence of mineralization upstream in the drainage basin. This grouping results in three categories according to the extent and type of mineralization in the drainage basin. A grouping on the basis of mineralization accounts for 15% of the total variation in the concentration of Mo in the sediment, suggesting that Mo-rich sediment is transported downstream from mineralized areas and exerts a major influence on the baseline concentration. Multiple samples are required to characterize each river because the withinstream component of variance comprises 54% of the total variance.Bottom sediment (minus 80 mesh) is a sensitive indicator of Mo mineralization; values of molybdenum as low as 2 ppm were considered anomalous for several rivers. A precise analytical procedure permits detection of concentrations of Mo in sediment approximately 2 ppm below the detection limit of the usual potassium pyrosulfate-thiocyanate procedure.  相似文献   

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