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1.
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   

2.
An investigation on the levels of mercury contamination in one species of the Cyanophyta, 14 species of the Rhodophyta, five species of the Phaeophyta and six species of the Chlorophyta from Penang waters indicated fairly low levels of bioaccumulated total mercury content. The bioaccumulated values ranged from below the detectable level to 0.35 μg g?1 except for Padina sp. 1 which demonstrated an amount equivalent to 1.025 μg g?1.These results indicate that the level of mercury contamination in the marine environment of Penang island falls within an acceptable range from the viewpoint of algal biodeposition.  相似文献   

3.
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   

4.
— The aims of this study were to estimate the total amount of mercury released to the environment during 60 years of gold mining (1867–1926) at Gympie, Queensland, Australia and to measure the mercury levels in soil samples surrounding the mining activity. We estimated that 1902 tonnes of mercury was released to the environment and about 1236 tonnes of which was released to the air. The mean mercury in the soil samples in the vicinity of the Scottish battery varied from 1.07 to 99.26 μg g?1 as compared to 0.075 μg g?1 as background mercury concentrations. The maximum mercury concentration measured in sediments of the Langton Gully was 6.12 μg g?1. These results show that large amount of mercury was used in this area during gold mining. Since mining is active in the area and Langton Gully flows into Mary River, we therefore, recommend that mercury concentration in air and fish should be monitored.  相似文献   

5.
Between January 1978 and September 1979 samples of subsurface (1 m) water and surface sediment were collected from sites in the North Sea, English Channel, Irish Sea and a number of estuarine areas. These have been analysed by fluorescence spectroscopy (UVF) in order to provide information on the levels of hydrocarbons generally present in UK marine waters.Total hydrocarbon concentrations (THCs) of water samples ranged from 1.1–74 μg l.?1 Ekofisk crude oil equivalents, all values greater than 3.5 μg l.?1 occurring inshore. In offshore areas the mean THCs were: 1.3 μg l.?1 in the northern North Sea, 1.5 μg l.?1 in the western Channel, 2.5 μg l.?1 in the eastern Channel and southern North Sea, and 2.6 μg l.?1 in the Irish Sea.THCs of sediment samples ranged from 0.27–340 μ g?1 dry weight Ekofisk crude oil equivalents, the highest concentration being in the Queen's Channel, the main entrance to the River Mersey.  相似文献   

6.
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   

7.
Total arsenic concentrations have been measured in macroalgae specimens from two coastal areas of South Australia. Phaeophyta in both areas were found to contain elevated arsenic concentrations (42.2–179 μg g?1 and 26.3–65.3 μg g?1) relative to Rhodophyta (17.6–31.3 μg g?1 and 12.5–16.2 μg g?1) and Chlorophyta (6.3–16.3 μg g?1 and 9.9–10.8 μg g?1).  相似文献   

8.
Deficient management of cinnabar mining left the San Joaquín region with high concentrations of mercury in its soils (2.4 – 4164 mg kg-1). Numerous cinnabar mines have contributed to the dispersion of mercury into agricultural (0.5 –314 mg kg-1) and forest (0.2 – 69 mg kg-1) soils. Sediments are a natural means of transportation for mercury, causing its spreading, especially in areas near mine entrances (0.6 – 687 mg kg-1). The nearness of maize crops to mines favors mercury accumulation in the different plant structures, such as roots, stems, leaves, and grain (0.04 – 8.2 mg kg-1); these being related to mercury volatilization and accumulation in soils. Mercury vapor present in the settlements could indicate a constant volatilization from lands and soils (22 – 153 ng m-3). The mercury levels found in the soils, in maize grain, and in the air resulted greater than the standards reported by the Official Mexican Norm (NOM) and the World Health Organization (WHO). Mercury in rainwater is due mainly to the presence of suspended atmospheric particles, later deposited on the surface (1.5 – 339 μg |-1). Mercury dissolution was found in the drinking water (10 – 170 ng |-1), with concentrations below those established by the NOM and the WHO. The contamination existing in the San Joaquín region does not reach the levels of the world’s greatest mercury producers: Almaden (Spain) and Idrija (Slovenia). It is, however, like that found in other important second degree world producers such as Guizhou (China). The population of San Joaquín, as well as its surrounding environment, are constantly exposed to mercury contamination, thus making a long term monitoring necessary to determine its effects, especially to people.  相似文献   

9.
Total mercury was analyzed as a function of body length, season, and diet in four commercially and recreationally important marine fish, bluefish (Pomatomus saltatrix), goosefish (Lophius americanus), silver hake (Merluccius bilinearis), and summer flounder (Paralichthys dentatus), collected from continental shelf waters of the northwest Atlantic Ocean. Mercury levels in the dorsal muscle tissue of 115 individuals ranged from 0.006 to 1.217 μg/g (wet weight) and varied significantly among species. The relationship between predator length and mercury concentration was linear for bluefish and summer flounder, while mercury levels increased with size at an exponential rate for silver hake and goosefish. Mercury burdens were the highest overall in bluefish, but increased with size at the greatest rate in silver hake. Seasonal differences were detected for bluefish and goosefish with mercury levels peaking during summer and spring, respectively. Prey mercury burdens and predator foraging habits are discussed as the primary factors influencing mercury accumulation.  相似文献   

10.
A survey of waters adjacent to this heavily urbanized and industrialized region showed concentrations of copper, 65 μg l.?1 to be the highest reported to date for estuarine waters, and lead up to 13.9 μg l.?1 Correlations between distributions of dissolved and total metal concentration in the water column, hydrography, and metal in the sediment were related to benthic studies in this area. Laboratory studies are cited which show the potential for adverse effects on marine animals at these metal concentrations.  相似文献   

11.
Methylmercury (MeHg) and inorganic mercury (Hginorg) were evaluated in the water of a Brazilian estuary, with two size classes of plankton and seven fish species of different feeding habits. Water partition coefficients (PCs) in microplankton were fourfold higher for MeHg than for Hginorg; and water PCs in mesoplankton were 26 times higher for MeHg than Hginorg. Difference between microplankton and mesoplankton MeHg bioaccumulation factor (BAF) was higher (0.60 log units) than Hginorg BAF (0.24 log units), indicating that trophic transfer of MeHg between planktonic organisms is more efficient than Hginorg transference. MeHg concentrations, proportion of mercury as MeHg and its biotransference factors (BTFs) in the microplankton, mesoplankton and fish increased with increasing trophic level while biotic concentrations of Hginorg and proportion of mercury as Hginorg decreased thus indicating that MeHg was indeed the biomagnified species of mercury. MeHg reflected the vertical trophic guilds distribution, due to the fact that the top predator fish presented the highest concentration (0.77 μg g−1 d.w.), followed by the less voracious species (0.43 μg g−1 d.w.); while planktivorous fish presented the lowest concentrations (0.044 μg g−1 d.w.). Hginorg did not present the same behavior. Results suggest that feeding habits and trophic guild are important parameters, influencing biotransference and biomagnification processes.  相似文献   

12.
Heavy metal concentrations in the tissues of marine turtles are presented. The most frequently monitored elements are mercury, cadmium and lead; and the tissues mainly analysed in nearly all the stranded individuals are muscle, liver and kidney. The highest mercury and cadmium levels were found in liver and kidney respectively; the majority of the lead burden existed in bones and carapace, while arsenic was present mainly in muscle tissue. Mercury occurred quite completely as methylmercury in muscle, whereas in liver the main form was the inorganic one. Arsenic was exclusively present in the metallorganic form either in muscle tissue or in liver. Metals in the eggs were mainly present in the yolk. Significantly higher concentration of mercury, copper, zinc and iron were found in yolk than albumen, while shell contained highest levels of manganese and copper. The load of trace metals in these animals strictly correlated with the species seems to depend on their different food behaviour.  相似文献   

13.
Crassostrea gigas spat were cultured for 8 weeks in the presence of a mixed algal diet in experimental tanks containing bis (tributyl tin) oxide (TBTO) alone, TBTO and a marine sediment, or a marine sediment alone. Growth measurements taken on a weekly basis showed enhanced weight gain in oysters exposed to nominal 50 and 100 mg l?1 concentrations of marine sediment alone. Spat in low level TBTO treatments (0.15 μg l?1) grew less well than the controls and showed pronounced thickening of the upper shell valve. High levels of TBTO (1.6 μg l?1) severely inhibited oyster growth. Tissue concentrations of TBT compounds were measured at the end of the experiment. Bio-concentration factors of 3000- and 10000-fold were demonstrated for the high and low TBTO treatments respectively.  相似文献   

14.
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   

15.
Total mercury, methyl mercury and sulphide contents of River Carron sediments (Lothian, Scotland) have been determined. Total mercury concentrations are comparable to other mercury polluted estuaries in the UK, but the methyl mercury values for low-sulphide Carron sediments are generally higher. It has been found that methyl mercury levels are initially in direct proportion to the sulphide concentrations of the sediments but beyond sulphide concentrations of 1.8 mg g?1 the methyl mercury levels decline sharply.  相似文献   

16.
Petroleum hydrocarbons in the sediments of the Bothnian Bay, Baltic proper, Öresund, Kattegatt and Skagerrak were analysed in a survey of oil pollution along the Swedish coast in 1974 and 1975. Sixty-one of these sediment stations were revisited in 1982 and analysed with the methods used in the first survey. The mean content of petroleum hydrocarbons (paraffin-naphthene fraction) in the sediment surface showed a statistically significant increase from 199 to 252 μg g?1 dry wt. The main increase had taken place in the coastal areas. Within 0–20 km distance of urbanized areas (>20 000 inhabitants) petroleum hydrocarbons had increased from 371 to 447 μg g?1. Sediment levels increased from 76 to 117 μg g?1, 20–50 km from urbanized areas. The increase in these areas was equivalent to 0.119 g m?2 yr?1.  相似文献   

17.
Samples of seawater from sites along the southwest coast were collected during 1984 and analysed for total tin and organotin by flameless atomic absorption spectro-photometry. Organotin concentrations were below detection limits (0.10 μg l?1 TBTO) at all marina sites, but higher concentrations were found in harbour waters, the highest value being 0.88 μg l?1 TBTO at Plymouth (Sutton harbour). The fact that organotin levels may occasionally exceed some toxicological threshold concentrations suggests that biological water quality may sometimes be depressed.  相似文献   

18.
Laboratory reared veliger larvae of the common mussel Mytilus edulis were grown for 15 days in filtered seawater containing 10 μg l?1, 1 μg l?1 and 0.1 μg l?1 tributyltin oxide (TBTO), the biocide in recent antifouling paint formulations. No larvae survived longer than 5 days in 10 μg l?1 TBTO or 10 days in 1 μg l?1 TBTO. Approximately half the larvae subjected to 0.1 μg l?1 TBTO were dead by day 15 (approximate 15 day LC50 = 0.1 μg l?1 TBTO) and most of the surviving larvae were moribund and had grown significantly more slowly than controls. It is noted that current recorded levels of TBT at several UK estuarine sites are higher than 0.1 μg l?1 and there has therefore probably been a high mortality of mussel larvae at such sites. The results are discussed in relation to the reported short-term toxicity of organotins to other marine organisms and the value of carrying out longer-term tests at low levels of TBT is pointed out.  相似文献   

19.
A 14?500 calendar year record of mercury accumulation rates has been obtained from an ombrotrophic peat bog in the Swiss Jura mountains. The range of natural (pre-industrial) mercury accumulation rates varied from 0.3 to 8.0 μg m−2 yr−1. During the Late Glacial and Holocene, climatic and volcanic signals were evident in the mercury record. Mercury accumulation rates increased by a factor of ca 5 during the Younger Dryas cold period. Short-term spikes in mercury accumulation rates, which correspond in time to known volcanic eruptions, occur during the late Boreal and Older Atlantic periods, when volcanic influences on mercury deposition appear to have been intensified due to increased atmospheric humidity. A correlation of mercury to bromine accumulation is observed throughout the pre-anthropogenic period. During the Holocene, mercury accumulation only exceeded the range of this correlation for a few short periods of elevated mercury deposition which correspond to known volcanic eruptions during the Older Atlantic. During historical times, mercury accumulation rates have exceeded the range of the correlation of mercury to bromine continuously since ca 1330 AD. This excess in mercury accumulation is interpreted as an indication of pollution. During the industrial period, mercury accumulation rates reached 107.6 μg m−2 yr−1, of which 84% was mercury that exceeded the correlation range. Mercury accumulation rates peaked again during the 1970s, with 78.8 μg m−2 yr−1. Early 20th century pollution appears to have been dominated by non-Swiss emissions from coal burning, whereas Swiss mercury emissions appear to have been the dominant pollution source during the mid and late 20th century. Current mercury accumulation rates at the site are similar to those ca 10 years ago, with modern deposition rates being ca 15 times their prehistorical average. Anthropogenic emissions of reactive brominated compounds could be contributing to increased atmospheric deposition rates of mercury.  相似文献   

20.
Total mercury was estimated in liver, gonads and muscle of some of the marine fishes from the Indian Ocean. The highest mercury concentration was observed in the muscle of sharks while the total mercury concentration was practically non-detectable in the liver and gonads. The range of all the values was 0.09–0.21 ppm (wet weight basis) and is quite low to reflect any possible mercury contamination.  相似文献   

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