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1.
Mercury（Hg） is well known as one of the most toxic elements to man.The coastal environments adjacent to industrial areas are reported to often be contaminated with mercury.Mercury becomes more toxic in the form of methylmercury（Me-Hg） which is converted from inorganic mercury in aqueous systems by microbial activity and can bio-magnify through the food chain.A simple method for the determination of total mercury and methylmercury in sediments was optimized by slightly modifying an old method using the direct mercury analyzer technique.Core sediment samples from Thane Creek,Mumbai,India were collected and analysed for total mercury and methylmercury.The Hg concentration in the creek varied between 0.54 to 16.03 μg g~（-1） while Me-Hg concentrations ranged between0.04 to 1.07 μg g~（-1）.In surface sediment,mercury concentrations ranged from 4.33 μg g~（-1） to 12.16μg g~（-1）.Total organic carbon content was found to be around 2 percent in different layers of the sediments.The enrichment factors,which indicate the extent of pollution in sediments,were estimated to range from 26 to 50 at different locations in the creek.Lithogenic and anthropogenic concentrations of mercury in the creek were also determined to compare the impact of anthropogenic and natural sources.Anthropogenic inventories were about 5-70 times more in concentration than the lithogenic in the different core sediments.  相似文献   

2.
Anomalously high levels of mercury in sediment in the Lenga estuary, Chile are comparable to the most contaminated sites previously reported elsewhere. Total mercury (Hgtotal) concentrations range from 0.5 to 129 mg kg−1 and organic mercury (Hgorg) from 11 to 53 μg kg−1. The highest levels are in areas near the previous wastewater outfall of a chlo-alkali plant. The results show that the proportion of Hgorg/Hgtotal in the sediment varies by more than two orders of magnitude (0.02–5.7%) according to the concentration of Hgtotal. No correlation between the concentration of Hgorg and Hgtotal was found. The lack of correlation does contrast with the findings of other authors in culture media. Our results indicate that even at very high concentrations of Hgtotal and organic matter do not influence organic mercury formation in estuary sediments. The disparity in Hgtotal and Hgorg concentrations also attests to environmental differences in the formation.  相似文献   

3.
The purpose of this study was to establish the distribution, speciation and bioavailability of mercury in mangrove sediments. A systemic survey of surficial sediments from 13 mangrove wetlands of China was carried out. Hg concentrations ranged from 2.3–903.6 ng g−1, with an average value of 189.4 ng g−1. Of the 13 areas surveyed, the Hg content in sediments was similar to background levels in 6 areas but was much higher in the other seven areas. Hg levels were affected by natural and anthropogenic factors, including terrestrial pollutants, geomorphic properties, and indirectly by economic status. Hg levels were positively correlated with organic matter, pH, and silt and clay fractions, but Hg was negatively correlated with sand fraction. In most mangrove wetlands, Hg existed primarily in the form of volatile Hg. Hg is easily bioaccumulated in mangrove wetlands and may be the natural source of Hg emissions to the atmosphere.  相似文献   

4.
季节性缺氧水库甲基汞的产生及其对下游水体的影响   总被引：14，自引：0，他引：14  
本文采用蒸馏-乙基化结合GC-CVAFS法对贵州红枫湖水库及其各入库和出库河流中的甲基汞时空分布和控制因素进行了研究.在春、秋、冬季节总甲基汞浓度和分布无明显时空变化,在0．053-0．333 ng／L之间.春季河流是水库甲基汞一个重要的输入源．夏季水库下层甲基汞显著升高,缺氧层最高值达0．923 ng／L.同时发现．缺氧层升高的甲基汞主要来自于水体自己产生或上层水体甲基汞的沉降,而不是来自于沉积物的释放．各季节湖水和河流样品的总甲基汞和溶解氧存在显著的负相关关系,Personal相关系数r为-0．81(n=78).在春、秋、冬季节溶解态甲基汞比例略低于颗粒态甲基汞,但在夏季,特别是缺氧层,甲基汞主要以溶解态存在．夏季河流入水经水库蓄水后,到再流出时已经富含甲基汞,出库河流中总甲基汞浓度已达到各入湖河流总甲基汞平均值的5.5倍,很明显在复季红枫湖已成为下游水体甲基汞的输入源,必将会对下游生态系统产生一定影响．  相似文献   

5.
《Marine pollution bulletin》2014,88(1-2):388-395
Distribution of sedimentary mercury in the Southern Baltic was investigated. Sediment samples were collected from the Southern Baltic in the period from 2009 to 2011, and concentrations of sedimentary total mercury (average 102 ng/g, range 5.8–225 ng/g) and methyl mercury (average 261 pg/g, range 61–940 pg/g) were measured in the manner that the influence of both patchiness and seasonal changes were assessed. Moreover, sedimentary mercury extracted with organic solvent- the so-called organic mercury was also analyzed (average 425 pg/g, range 100–1440 pg/g). There is a statistically significant dependence between organic mercury and both methyl mercury and total mercury concentrations in the sediments. Methyl mercury contribution to total mercury varied from 0.12% to 1.05%, while organic mercury contributed to 2% of total concentration on average. The area studied, although mercury concentrations exceed threefold the geochemical background, can be regarded as moderately contaminated with mercury, and methylmercury.  相似文献   

6.
Mercury releases into Lavaca Bay resulted in public health notices and a fishing closure for crabs and finfish. Mercury containing wastewater discharges were halted in 1970, but sediments were contaminated with mercury. The sediments are a source of mercury to the benthic food web via methylation. Mercury in water column feeding organisms has decreased markedly. Concentrations in benthic food web organisms remain elevated. Human consumption concerns for oysters have ended, but a closure for fishing for crabs and finfish continues. Monitoring of mercury in organisms since 1977 shows a gradual downward trend in mercury in crabs and finfish, but this was not sufficient to remove the closure. Continued releases of mercury, man's activities, and resuspension of sediments keep mercury in the sediment's biologically active zone. This enables the uptake of mercury via the benthic food web. If releases are ended, it will take years for the mercury to decrease to concentrations not of concern for human consumption. If more remediation to reduce the mercury concentrations in the sediments takes place, decrease of mercury in the organisms might occur more quickly.  相似文献   

7.
Thirteen surface sediment samples from a shallow, semi-enclosed bay, Gunnekleivfjorden, South-West Norway, were analysed for total mercury. The concentrations ranged between 90 and 350 ppm dried sediment. The median value (250 ppm mercury) is more than twice the median value of sixteen sediment samples collected in Minamata Bay in 1963. The surface area of Gunnekleivfjorden is approximately 1 km2, implying that minimum 10 tons of mercury is accumulated in the upper 5 cm of the sediments of the bay. The extensive contamination is caused by discharge of inorganic mercury from a chlor-alkali plant during the last 25 years.  相似文献   

8.
Total mercury (Hg) and methylmercury (MeHg) were analyzed in near surface sediments (0-2 cm) and biota (zooplankton, macro-invertebrates, finfish) collected from Narragansett Bay (Rhode Island/Massachusetts, USA) and adjacent embayments and tidal rivers. Spatial patterns in sediment contamination were governed by the high affinity of Hg for total organic carbon (TOC). Sediment MeHg and percent MeHg were also inversely related to summer bottom water dissolved oxygen (DO) concentrations, presumably due to the increased activity of methylating bacteria. For biota, Hg accumulation was influenced by inter-specific habitat preferences and trophic structure, and sediments with high TOC and percent silt-clay composition limited mercury bioavailability. Moreover, hypoxic bottom water limited Hg bioaccumulation, which is possibly mediated by a reduction in biotic foraging, and thus, dietary uptake of mercury. Finally, most biota demonstrated a significant positive relationship between tissue and TOC-normalized sediment Hg, but relationships were much weaker or absent for sediment MeHg. These results have important implications for the utility of estuarine biota as subjects for mercury monitoring programs.  相似文献   

9.
Pre-exposure of marine mussels to low levels of mercury (0.5 μg l?1 and less) enhanced their tolerance to more toxic levels. Seawater mercury concentrations similar to our experimental pre-exposure levels have been reported in mercury-contaminated areas where mussels presently exist. A higher pre-exposure concentration (5 μg l?1) was not effective in inducing enhanced mercury tolerance. The relative effectiveness of pre-exposure concentration in inducing enhanced tolerance was related to induction of mercury-binding proteins, the degree of saturation of mercury on the proteins, and the extent of binding of mercury to other subcellular fractions.  相似文献   

10.
A sampling and measuring device which enables the assessment of atmospheric particulate and gaseous mercury concentrations has been tested on Mount Etna Volcano. Particulate matter is collected on a Whatman GF/C of 1.0 µm pore-size, gaseous mercury species on a Au-column. The analysis is carried out in two steps: (1) the mercury species collected on the filter or the Au-column are transferred to a fixed analytical Au-column; (2) mercury liberated from this column during the second step is detected with a Mercury Vapour Monitor. Average concentrations of gaseous and particulate mercury in ambient sampling sites on Mount Etna are 3.8 ng m?3 and 0.49 ng m?3 respectively. Average concentrations of gaseous and particulate mercury in the plume of Bocca Nuova on Mount Etna are 15 ng m?3 and 24 ng m?3 respectively. An estimation of the total mercury discharge from Mount Etna amounts to 2.5 10?2 tons day?1.  相似文献   

11.
The role of sulphide-containing species in sediments in the mobilization of mercury in the environment is demonstrated. The mobile species is the volatile hydrophobic dimethyl mercury. Transport to atmosphere in this form may account for a loss of about 12% annually of methyl mercury from sediments and may therefore be a substantive part of the biogeochemical cycling of mercury in the environment.  相似文献   

12.
This article presents results of mercury in surface waters from Hunza River basin, Northern Areas, Pakistan. Small‐scale gold mining activities along the Hunza and Gilgit rivers are long known to be discharging mercury in the amalgamation and roasting processes. Previous studies reported high mercury concentrations in soils close to mining operations as well as serious health problems for miners. However, none of the studies have focused on the level of contamination in aqueous environments. This is the first study on the investigation of source and fate of sediment and river‐borne mercury in the Hunza River. The samples collected near gold panning sites showed higher mercury concentrations than critical levels established by the U.S. Environmental Protection Agency. The observed dissolved mercury concentrations ranged from 5.10 to 25.25 ng/l, whereas particulate‐bound mercury ranged from 4.85 to 154.62 ng/l. Particulate‐phase mercury corresponded to more than 75% of the total observed mercury concentrations for all of the sampled rivers. Thus, suspended sediments represented the major pathway of the riverine mercury transport. A mass balance calculation suggested an annual mercury flux of 48.6 g/km2 into the Hunza River basin. The samples collected from the most affected river, the Shimsal River, averaged to have 108 ng/l total mercury. This amount was close to the average soil mercury data of 151 ng/l as reported by the Pakistan Mineral Development Corporation in 2001. The dominant source of contamination was shown to be the leaching of large quantities of mercury from the mercury‐rich sediment and flood plain soil into the rivers, rather than the direct release from mining activities. Significant decrease in both dissolved and particulate‐bound mercury concentration downstream of Attabad Lake suggested that mercury is being accumulated or consumed in the lake. Although minimization or elimination of mercury loses from the mining process seems important for the well‐being of the miners, preventing the remobilization of accumulated mercury is equally important in mercury control in this region. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

13.
The mercury content in the marine phanerogam Posidonia oceanica, sampled in an area near a chloralkali complex, has been measured and compared with that of the samples collected in a non-impacted region.Plants growing in the seawater facing the chlor-alkali complex showed mercury content of 0.19 μg g−1 f.w., compared with 0.02 μg g−1 f.w. in the samples from the control area. Sediments of the industrial area have mercury levels 20–30 times higher than those from the control area. As the mercury concentration in seawater of both areas is comparable, the mercury content in the plant appears to be correlated with mercury levels in the sediment; probably the metal uptake in Posidonia oceanica takes place mainly through the root system.  相似文献   

14.
Sediment (surface and core) sampling was conducted during the period from August 96-December 98 from intertidal and offshore areas in Kuwait Bay. The highest (and most variable) concentrations of total mercury (T-Hg; 36500+/-34930 ng g(-1)) are encountered around the previous industrial outfall where sediments are disturbed by shipping activities. The concentrations of T-Hg are lower in the Shuwaikh Port area (650+/-210 ng g(-1)) and continue to decrease towards the northern coastline of Kuwait Bay (average concentrations in the wider Bay region are 50+/-30 ng g(-1)). These values are still above background concentrations of 15-20 ng g(-1). Calculation of the total inventory of mercury in all the surface sediments of the studied area indicates that approximately 22.5 ton is present which is similar to the estimated industrial discharges of approximately 20 ton suggesting that the contamination is largely confined to the Bay and that releases to the wider Gulf region are small. The distributions of MeHg are similar to those of T-Hg and represent ranges between 0.23% and 0.5% of the T-Hg indicating that surface sediments within Kuwait Bay contain approximately 80 kg of this chemical.  相似文献   

15.
Studies were initiated in May 1975 to determine the impact of a new nickel refinery on ambient mercury level in sediments taken from Halifax Bay, Australia. Although mercury levels were relatively low in all samples, surface sediments were found to contain 2.5–3.0 times the mercury concentration of subsurface samples. However, surface sediment samples collected adjacent to the refinery outfall within the first three weeks of continuous discharge showed significant increases in mercury levels when compared with surface samples taken from areas not affected by the refinery.  相似文献   

16.
Anthropogenic mercury pollution was studied in Kastela Bay (Croatia), 10 years after chloralkaline plant (PVC) stopped production. The concentration of total mercury determined in sediments which are composed mainly of calcite and quartz, are in the range 14,280-30,400 ng/g. The values are higher than reported in the literature for Elbe and Seine estuaries and also above 25,000 ng/g used for criterion in remediation project in Minamata Bay. The concentration of methylmercury 6.05-36.74 ng/g are typical for slightly to highly contaminated estuarine sediments. The low ratio of methylmercury to total mercury found in sediments of Kastela Bay is in the range 0.04-0.18%. It can be explained that in this region predominate conditions which do not promote in-situ methylation. Sediments were found to be highly anoxic. Concentrations of total mercury in unfiltered surface waters are in the range 69-145 ng/l and in unfiltered bottom waters in the range 230-1,418 ngl(-1). High concentrations found in bottom waters suggest that either resuspension or partial dissolution of sediments takes place. An experiment performed on filtered and unfiltered waters showed that about 85% of total mercury in surface water and almost 100% in bottom water was retained on 45 microm filters. To demonstrate contrasts, two pristine estuaries from norths and south Europe were studied. Silicious sediments of Ore estuary (Sweden) and calcareous sediments of Krka estuary (Croatia) have total mercury concentrations close to accepted background level. The ratio of methylmercury to total mercury is < or = 1% in all samples with one exception. The highest observed ratio (2.70%) was in the surface sediment from E2 station in Krka estuary measured in March 2000. This location is suitable for studying methylmercury formation in pristine environment.  相似文献   

17.
The focus of this work is to explore the use of the netted whelk, Nassarius reticulatus (L.), as an indicator of mercury (Hg) contamination, by assessing the concentration of Hg in the sediments and in the whelk along the entire Portuguese coast. Total Hg concentrations ranged from below the detection limit (0.01 ng absolute mercury) up to 0.87 mg kg(-1) dry weight (dwt) in sediments and between 0.06 and 1.02 mg kg(-1) (dwt) for organisms, with no significant differences between males and females. Although organic mercury was not detected in the sediments, it represented, on average, 52% of the total Hg in the whelk tissues, and as high as 88% in some cases, suggesting mercury accumulation from dietary intake. Significant negative correlations were found between the total Hg concentrations in the sediments and the log(10) of Hg concentrations in whelk tissues males (r=-0.64; P<0.01) and females (r=-0.52; P<0.01) indicating that the species is a poor indicator of Hg contamination. Nevertheless, since the highest concentrations of organic mercury in the whelk tissues were found in the least contaminated areas, this species must be highly relevant in the trophic web, namely on the possible biomagnification of mercury. The high dietary mercury accumulation from feeding on carrion and the low bioavailability of mercury to whelks in estuarine sediments may be the basis of the mercury accumulation pattern in N. reticulatus.  相似文献   

18.
The muscle tissue of snapper (Chrysophrys auratus: Sparidae) from two areas of the New South Wales coast was analysed for methyl mercury, total mercury and selenium concentrations (134 samples from the Sydney area and 186 samples from the Nowra area, about 120 km to the south of Sydney).

The Sydney snapper ranged from 0.08 to 1.66 mg kg−1 total mercury (mean 0.32 mg kg−1), while the Nowra snapper ranged from 0.01 to 0.78 mg kg−1 total Hg (mean 0.11 mg kg−1). These latter results appear anomalously low relative to other studies in Australia and New Zealand.

Methyl mercury averaged 94.7% of the total mercury content of the Sydney snapper, and 91.3% for the Nowra snapper.

The concentrations of selenium in the muscle tissues of snapper from both areas were similar and did not increase with increasing mercury concentrations. The highest selenium concentration was 0.85 mg kg−1.  相似文献   


19.
Total mercury concentrations were determined in a variety of fish and invertebrates and two dugongs from the coastal waters of Townsville on the N.E. coast of Australia. Fish generally contained the highest levels of mercury with 50% of the sharks examined having muscle concentrations above 0.5 μg g?1 wet weight. A significantly positive correlation was found between muscle levels and body length in sharks. Seventy per cent of the teleosts examined contained less than 0.2 μg g?1 in their muscle tissue and only 7% were above 0.5 μg g?1. Mercury concentrations in teleost liver were significantly positively correlated with muscle levels. Of the invertebrates examined, the cephalopod molluscs contained the highest levels although none exceeded 0.5 μg g?1. Mercury levels in the dugong were extremely low compared with most reported values for other marine mammals. It was concluded that the area contained mercury levels slightly above those considered normal for a non-contaminated marine environment.  相似文献   

20.
Surveys of natural populations of mussels have identified areas of mercury contamination in the Firth of Forth, Scotland. A field bio-assay technique has been devised which accurately reflects the mean total mercury concentration in the surrounding seawater. The detection limit of the technique is estimated at 5–20 ng Hg l.?1, and consequently the method can detect comparatively small enhancements over background mercury concentrations in estuarine and sea water.  相似文献   

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