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1.
In order to characterize our study area and to provide reference values to be used in the future to measure the changes produced by an increase in contamination, the concentrations of chlorinated hydrocarbons have been investigated in fifty-one samples of seawater, taken at four different depths: air-sea interface, surface, one metre and bottom waters, and in twenty-three samples of surface sediments from Blanca Bay, Argentina. Of eleven organochlorine compounds we were looking for (α BHC, lindane, heptachlor, δ BHC. aldrin, heptachlor epoxide, dieldrin, o-p′DDD, p-p′DDD, o-p′DDT and p-p′DDT), seven could be detected in seawater and three in surface sediments with the following mean concentrations: α-BHC=48·2 ng l?1; lindane=54·2 ng l?1; heptachlor=45·0 ng l?1; δ BHC=12·5 ng l?1; aldrin=61·8 ng l?1 and ΣDDT=67·0 ng l?1; and δ BHC=3·2 ng g?1; lindane=4·2 ng g?1 and heptachlor=1·0 ng g?1 for seawater, regarding the surface waters, and sediment samples, respectively.Concentration factors among the different water layers were also studied to see if there was any correlation between chlorinated hydrocarbon contents and the water depths from which the samples were taken. As a mean value, the air-sea interface water contains 18 times more of these compounds than that of the water near the bottom. A comparison of the values corresponding to seawater and surface sediments from our study area with those levels measured in samples from other geographic locations is also presented.With the purpose to detect a relationship between chlorinated hydrocarbon concentrations and the contents of particulate matter (PM) on the one hand, and particulate organic material (POM) on the other hand, four groups of samples containing different amounts of PM and POM, respectively were formed. From a comparison of the results obtained, lindane, heptachlor and δ BHC showed a tendency to lower concentrations in those samples containing little PM whereas α BHC and aldrin remained without important changes. No significant correlation was found between organochlorine levels and contents of POM.  相似文献   

2.
厦门筼筜湖纳潮排污能力研究   总被引：4，自引：0，他引：4  
自 1 971年围垦后 ,厦门港成为内湖 ,没有海水进出交换 ,从而积蓄多种有机污染物和重金属 .但自从 1 984年采取纳潮排污后 ,该湖水质有所改善 .本研究于1 999年主要对湖水质进行调查和评价 .结果显示污染物含量虽然有所降低 ,但仍属于污染状态 .其纳潮排污 ,每天可排放出 :石油烃 40 .8kg ,有机氯农药 0 .0 1 1kg ,铜 4.54kg ,铅 0 .2 84kg ,锌 1 1 .97kg ,镉 0 .3 6kg ,汞 0 .0 1 1kg .由于湖水水质仍未完全改善 ,非常有必要继续进行监测 .  相似文献   

3.
Bioassays were conducted with sea urchin and sand dollar sperm to determine the toxicity of chlorinated and unchlorinated sewage effluent and chlorinated and brominated seawater. The sperm cells were exposed to seawater dilutions of each toxicant for 5–15 min. The fertilisation of eggs served as the indicators of sperm viability. The effective concentrations which reduced fertilisation success by 50% (EC50) averaged 2·2 and 4·8% chlorinated and unchlorinated sewage in seawater, respectively. The sperm cells were extremely sensitive to chlorinated seawater at concentrations from 0·002 to 0·020 mg/litre total residual oxidant (TRO). Brominated seawater proved toxic to sperm in one test at 0·015 mg/litre TRO. Results of the sperm bioassays are compared with previous acute and chronic bioassays with fish.  相似文献   

4.
The presence of electrolytes (salts) in aqueous solution modifies the solubility and related properties of organic compounds in water. Reported data for salting-out constants (Setschenow constants) which relate solubility to the salt concentration of aromatic and alkane hydrocarbons, and their chlorinated derivatives, and some organic acids have been compiled for 25 aqueous salt solutions at 20–25 °C. The salting-out sequences for various electrolytes are discussed and it is shown that the salting-out effect is greater for organic solutes with large molar volumes. A compilation of salting-out constants for NaCl solutions and seawater (natural or synthetic) with a variety of solutes, shows that the Setschenow constants are similar for natural or artificial seawater (at salinity of 30–35%.) and NaCl solutions (at 3.0–3.5% or 0.5 M). A simple correlation is suggested for estimating the Setschenow constants for a variety of organic solutes in seawater which typically yields a reduction in solubility by a factor of 1.36. The hydrophobicity of organic solutes is therefore increased by this factor, as is the air-water partition coefficient, implying an increased partitioning from aqueous solution into air, organic carbon and lipid phases. The effect must be quantified when comparing the behavior of organic contaminants in freshwater and marine conditions.  相似文献   

5.
An ion-exchange technique was used to concentrate ammonia from seawater. Precipitation of bivalent cations, prior to concentration, reduced the variability of ammonia recovery from the ion-exchange column and lengthened column life. Analysis of the eluate was by the phenolhypochlorite reaction. The method was designed for use with small seawater samples (>10ml) and has the advantage that it can be adapted for use with small volumes of seawater with no loss in sensitivity. In a 10 ml seawater example NH3-N concentrations of 10–150 μg l?1 were accurately determined.  相似文献   

6.
Behavioral responses to chemically dechlorinated seawater were studied using two species of marine fish associated with power plant discharge areas off Southern California. Opaleye (Girella nigricans) neither avoided nor were attracted to chlorinated seawater containing 0·1 mg/liter total residual oxidants (TRO) which had been dechlorinated using equimolar or excess sodium thiosulfate. Blue-banded goby (Lythrypnus dalli) did not avoid dechlorinated seawater initially containing 0·1 or 0·9–1·0 mg/liter TRO. Previously it has been shown that opaleye avoided chlorinated seawater with oxidant concentrations of 0·1 mg/liter and blue-banded gobies avoided 0·9–1·0 mg/liter TRO. Elimination of chlorine-produced oxidants by thiosulphate dechlorination resulted in 100% survival in both species. The toxicological implications of exposure to dechlorinated seawater are discussed.  相似文献   

7.
The vertical transport of PCBs and chlorinated hydrocarbon pesticides such as DDT compounds and HCH (BHC) isomers in the deep sea are discussed on basis of their vertical profiles and the proportion of their adsorbed and dissolved fractions in surface water surveyed in the Western Pacific, Eastern Indian and Antarctic Oceans.All chlorinated hydrocarbons determined were detected with measurable concentrations throughout the water column, even at depths of several thousand meters. The vertical distributions of PCBs and DDT compounds were found to show small variations in concentration throughout the water column, whereas HCH isomer concentrations decreased systematically with depth. A large portion of DDT compounds in surface water was adsorbed on suspended solids, while most of the HCH isomers were present in the filtered water. The proportion of PCBs adsorbed on suspended solids was smaller than the proportion of DDT compounds, but was much greater than that of HCH isomers. These observations suggest that HCH isomers have been slowly scavenged from the surface to the deeper layers in the water column, while PCBs and DDT compounds have been rapidly and abundantly transported downward by sinking particles.The percentages of chlorinated hydrocarbons adsorbed on suspended solids in surface water increased towards the high latitude locations, and the percentage seemed to be proportional to the concentration of suspended solids in the surface water. This implies that the residence time of chlorinated hydrocarbons in the water column will differ significantly among oceans that differ in primary productivity. According to our estimation based on the data presented in this study, the residence time ofHCH in the euphotic zone, the top 100 m of the water column, is more than 2 years, whereas those of PCBs andDDT are less than 1 year. The longest residence time, of from 5 to 10 years, was obtained forHCH in oligotrophic water of the western North Pacific. The shortest value, only 11 to 19 days, was estimated forDDT in the Antarctic Ocean.  相似文献   

8.
Concentrations of petroleum hydrocarbons in seawater from the general region between Nova Scotia and Bermuda were estimated using fluorescence spectroscopy. Concentrations in surface water (0–3 mm) averaged 20.4 μg/l, and in water from 1 and 5 m they averaged 0.8 and 0.4 μg/l respectively. No significant concentrations could be detected in deeper water. There was considerable variability in the concentrations suggesting that the distribution of oil in seawater is quite patchy, especially in surface waters. Seawater samples for hydrocarbon analysis cannot be collected with conventional sampling equipment. Due to adsorption problems, the inner surface of samplers must come into contact only with the water being sampled and must be rinsed with organic solvent after samples are removed. Because these precautions were not taken in previous investigations, much of the published data of hydrocarbons in seawater is unreliable.  相似文献   

9.
Plankton samples (20-350 microm and >350 microm) collected at three transects along the Galician coast (NW Spain) were analysed for individual aliphatic and aromatic hydrocarbons by GC-MS. Sample collection was performed in April-July 2003, after the Prestige oil spill (November 2002), to determine whether the hydrocarbons released into the water column as a consequence of the spill were accumulated by the planktonic communities during the subsequent spring and early summer blooms. Surface sediments were also collected to assess the presence of the spilled oil, removed from the water column by downward particle transport. Plankton concentrations of PAHs (Sigma14 parent components) were in the range of 25-898 ng g(-1)dw, the highest values being close to coastal urban areas. However, the individual distributions were highly dominated by alkyl naphthalenes and phenanthrenes, paralleling those in the water dissolved fraction. The detailed study of petrogenic molecular markers (e.g. steranes and triterpanes, and methyl phenanthrenes and dibenzothiophenes) showed the occurrence of background petrogenic pollution but not related with the Prestige oil, with the possible exception of the station off Costa da Morte in May 2003, heavily oiled after the accident. The dominant northerly wind conditions during the spring and early summer 2003, which prevented the arrival of fresh oil spilled from the wreck, together with the heavy nature of the fuel oil, which was barely dispersed in seawater, and the large variability of planktonic cycles, could be the factors hiding the acute accumulation of the spilled hydrocarbons. Then, with the above exception, the concentrations of PAHs found in the collected samples, mostly deriving from chronic pollution, can be considered as the reference values for the region.  相似文献   

10.
A highly sensitive flow injection analysis (FIA) method for determining the concentration of iron in seawater has been developed. The technique is a modification of the catalytic batch method previously reported by Hirayama and Unohara. By optimising the chemistry for FIA and incorporating in-line preconcentration of the iron from seawater onto a column of resin-immobilised 8-hydroxyquinoline, the detection limit of the method has been reduced to 0.025 nM. The typical precision of the method for a 0.35 nM Fe sample is 2.5% (n = 6). The method has been used at sea in its preconcentration mode to determine iron in open ocean water samples from the equatorial Pacific and the North Atlantic. It has also been used in a direct injection mode for hydrothermal plume samples from around Loihi Seamount in the Central Pacific.  相似文献   

11.
In September 1994 and 1995, scientists from the Australian Institute of Marine Science (AIMS) and the Australian Geological Survey Organization (AGSO) conducted surveys aboard the RV Lady Basten to determine the dispersion, fates and effects of produced formation water (PFW) discharged from the ‘ Harriet A ’ oil production platform near the Montebello Islands. This report is one of four related papers and describes the non-volatile hydrocarbon chemistry studies. The dispersion of the PFW into dissolved and particulate fractions of seawater were measured using moored high volume water samplers, surface screen samplers and moored and drifting sediment traps. Bio-accumulation was studied using transplanted oysters, and dispersion measured into sediment with benthic grabs.Results showed enrichment in non-volatile hydrocarbons in surface microlayer samples to a distance of 1·8 km in the direction of tidal flow. Concentrations in surface microlayers near the platform varied by an order of magnitude and corresponded to when a surface slick was visible or not visible. Concentrations of oil in seawater ranged from 2·0 to 8·5 μg l−1at near stations to 1·3 μg l−1at 1·8 km. Water column samples showed the processes of desorption from particles for soluble components occur within the range of 1·8 km. Most particulate hydrocarbons drop out of suspension within c. 1 to 2 km from the platform. Fluxes of particulate hydrocarbons through the water column at c. 1 km, as estimated by moored sediment traps in 1995, were 138 to 148 ng cm−2day−1. A decrease in sediment concentrations within c. 1 km of the platform was measured as 2·45±1·29 μg g−1dry wt (n=15) in 1994 to 0·86±0·54 μg g−1dry wt (n=21) in 1995, after the platform installed a centrifugal separator in the discharge treatment process. Thus the residence time of this relatively low molecular weight oil was estimated in the coarse aerobic sands surrounding the platform to be less than one year. Oysters suspended near the platform bio-accumulated hydrocarbons and other lipophilic organics in their tissues. Uptake rates and bio-concentration factors of hydrocarbons indicated potential toxicity at the near-field stations within c. 1 km radius.A mass balance was constructed to show the partitioning of the input of hydrocarbons from the PFW into the surrounding marine ecosystem. The rates of dissipation processes were estimated as follows: dilution from tidal currents>degradation in the water column>sedimentation>evaporation. The calculations based on maximum concentrations measured in the environmental samples accounted for 85% of the daily input suspended within a 1 km radius.It is estimated that the potential zone of toxic influence in the water column extends to a distance of approximately 1 km. Concentrations of oil in sediments were too low to indicate potential toxicity. By the collaborative application of oceanographic and geochemical techniques to marine environmental problems, we endeavour to provide effective feedback to the oil industry to gauge the effectiveness of their operational strategies in minimizing impact in these pristine regions.  相似文献   

12.
Four experiments were carried out to determine the effect of different temperatures, light levels and biological activities on the residence times of petroleum hydrocarbons. No. 2 fuel oil was added as a seawater dispersion to give an initial concentration of 150 to 300 μg/litre in the water columns of large, outdoor marine microcosms. Hydrocarbons in water samples fractionated on passage through glass fibre filters (0·3 μm pore size) according to the solubilities, so that 80–90 % of the aromatics entered the filtrate while all of the saturates were trapped by the filter. The removal of oil compounds from the water columns was exponential, with rates which appeared to be determined chiefly by the temperature. The half life of total hydrocarbons varied from more than 10 days in March to ～30 h in July and September. Volatilisation was hypothesised to be an important removal mechanism for the 40–60% of the saturates which were not sedimented with suspended particulate matter. In warm water, the residence times of normal alkanes were increased up to 50 % by poisoning the water column, but no similar increase was noted for the bulk of the F1 hydrocarbons. Aromatic (F2) hydrocarbons appeared to be removed slowly volatilisation from cold water (t12 > 200 h) and rapidly by biodegradation from warm water (t12 < 40 h).  相似文献   

13.
Sea-surface microlayer samples were collected from six nearshore areas receiving different amounts of anthropogenic inputs. The samples were analyzed for selected trace metals, chlorinated hydrocarbons, and polycyclic aromatic hydrocarbons. The relative toxicities of the samples were determined with fish embryo bioassays.Contaminant concentrations generally increased from offshore to the inshore stations. Contaminant concentrations were several orders of magnitude higher in microlayer samples from the highly industrialized Los Angeles and Long Beach harbors compared to samples from a site 15km offshore. Microlayer samples from the inshore stations were significantly more toxic, and induced significantly more developmental abnormalities and chromosome aberrations, than samples from the offshore stations.  相似文献   

14.
Eggs from 69 females of spring spawning herring from the German Baltic coast (Travemünde, April 1979) were incubated in clean sea water (20‰ S, temperature 8°C) under standard conditions. Sixty-one trials could be used for the evaluation of hatching success. Viable hatch was taken as a measure to evaluate the effects of chlorinated hydrocarbons accumulated in gonads, liver and muscle of parental fish.PCB levels in running ripe females ranged on a wet weight basis between 19 and 241 ng g?1 (gonad), 20 and 377 ng g?1 (liver) and 11 and 1820 ng g?1 (muscle). Concentrations of other chlorinated hydrocarbons (DDD, DDE, γ-HCH, etc.) were in the same range as reported by other authors for Baltic herring (Huschenbeth, 1973, 1977). Viable hatch was significantly affected at ovary DDE concentrations higher than 18 ng g?1 (wet wt) and PCB concentrations of more than 120 ng g?1 (wet wt).Results are compared with data obtained during earlier investigations with flounder eggs.  相似文献   

15.
对用液上空间气相色谱法测定海水中的卤代烃进行了研究，对影响气相中卤代烃的一些重要因子作了分析探讨，作为检验该方法的优越性，以青岛胶州湾为实例，测定了表层分布卤代烃。  相似文献   

16.
Studies on the biogeochemical cycling of organic contaminants in the Mediterranean have demonstrated the importance of polychlorinated biphenyls (PCBs) as relatively stable markers of recent anthropogenic influence in ocean systems. This paper presents results of hydrocarbon analyses of deep water profiles, sediments and their associated surface flocculent layers, and zooplankton samples collected in the western basin. Seawater concentrations were higher than those previously reported for the eastern basin and were consistent with the presence of industrial sources in the northwestern segment. In the water column, the percent of PCBs associated with filterable particles was related to the ambient concentrations of total suspended matter, distance from coastal input sources and on depth. The occurrence of deep water residues primarily in the dissolved phase and observations of subsurface maxima in seawater concentrations during a season of high surface productivity were consistent with the predictions of vertical transport models based on residues associated with sinking particles and equilibrium partitioning. Flocculent layers at the sea/sediment interface contained two and three orders of magnitude, respectively, more PCBs and petroleum hydrocarbons (PHCs) than their associated surface sediments. The flocculent particles also contained several biogenic hydrocarbons presumably originating from plankton and relatively soluble and labile contaminants such as hexachlorohexane isomers (HCH) and hexachlorobenzene (HCB), thus confirming that the majority of the flux of hydrocarbons to sediments is carried on rapidly settling large particles. By combining the sediment and flocculents data with published sedimentation rates for the deep basins of the Mediterranean, a yearly flux rate of PCBs to the open sea sediments was estimated as 13 μg m−2 yr−1 or less than half of the rate measured in a coastal sediment trap experiment. Analytical results are placed in the context of other distribution data for PCBs and long-term flux studies to construct a partial mass balance budget for this semi-enclosed sea. The computed coastal inventory showed that about 35% remains suspended in the water column while the majority of residues are deposited in coastal sediments. However in the open sea, the deep water column may contain up to 70% of the total inventory and may be a continually increasing reservoir of stable organic contaminants reaching the ocean. The budget shows that priority for improved research and monitoring efforts in ocean systems should be given to continued advancement in techniques for the precise measurement of deep water concentrations and for measuring current atmospheric inputs and sedimentation rates in order to develop more accurate ocean flux models.  相似文献   

17.
Two sampling devices for the in situ extraction of chlorinated hydrocarbons from water are described. Both samplers use the macroreticular adsorbent Amberlite XAD-2. They include a “fish” sampler which has been used to collect samples for PCB analysis from waters around the British Isles. Operation of this sampler causes a minimum of interruption to a ship's cruise programme and at the same time allows a large area to be surveyed. The second sampler is a self-powered in situ pump which is cheap to construct and can be left unattended to extract large volumes of water at a fixed station. The device is serviced by divers and samples may be collected daily on a routine sampling basis.  相似文献   

18.
An intercomparison study of voltammetric and atomic absorption spectrometric methods for determining cadmium, lead and copper in seawater samples was conducted. The voltammetric approach utilizes differential pulse anodic stripping voltammetry using a rotating, glassy carbon, mercury film electrode under conditions developed to minimize contamination sources and to enhance sensitivity for seawater matrices. The atomic absorption approach involves a concentration step using either an organic solvent extraction of metal dithiocarbamate chelates or a Chelex-100 column with detection by graphite furnace atomic absorption spectrometry. Similar and consistent results were obtained using both methods for the three trace metals studied on a wide range of natural seawater samples. Both methods are comparable in sensitivity for cadmium and copper, however the voltammetric method is better suited for the analysis of lead in seawater because of its enhanced sensitivity and low blank. An advantage of the voltammetric approach is its amenability towards real-time shipboard analysis.  相似文献   

19.
A sensitive method for iron determination in seawater has been adapted on a submersible chemical analyser for in situ measurements. The technique is based on flow injection analysis (FIA) coupled with spectrophotometric detection. When direct injection of seawater was used, the detection limit was 1.6 nM, and the precision 7%, for a triplicate injection of a 4 nM standard. At low iron concentrations, on line preconcentration using a column filled with 8-hydroxyquinoline (8HQ) resin was used. The detection limit was 0.15 nM (time of preconcentration = 240 s), and the precision 6%, for a triplicate determination of a 1 nM standard, allowing the determination of Fe in most of the oceanic regimes, except the most depleted surface waters. The effect of temperature, pressure, salinity, copper, manganese, and iron speciation on the response of the analyser was investigated. The slope of the calibration curves followed a linear relation as a function of pressure (Cp = 2.8 × 10− 5P + 3.4 × 10− 2 s nmol− 1, R2 = 0.997, for Θ = 13 °C) and an exponential relation as a function of temperature (CΘ = 0.009e0.103Θ, R2 = 0.832, for P = 3 bar). No statistical difference at 95% confidence level was observed for samples of different salinities (S = 0, 20, 35). Only very high concentration of copper (1000 × [Fe]) produced a detectable interference. The chemical analyser was deployed in the coastal environment of the Bay of Brest to investigate the effect of iron speciation on the response of the analyser. Direct injection was used and seawater samples were acidified on line for 80 s. Dissolved iron (DFe, filtered seawater (0.4 μm), acidified and stored at pH 1.8) corresponded to 29 ± 4% of Fea (unfiltered seawater, acidified in line at pH 1.8 for 80 s). Most of Fea (71 ± 4%) was probably a fraction of total dissolvable iron (TDFe, unfiltered seawater, acidified and stored at pH 1.8).  相似文献   

20.
To determine if avoidance of chlorinated seawater by fish resulted in physiological protection from toxicity, studies were carried out which assessed (a) changes in the routine oxygen consumption rate and (b) the ability of treated fish to successfully compete with untreated conspecifics for a limited food resource.Temperate marine damselfish, Chromis punctipinnis, were exposed to stepwise increasing levels of chlorinated seawater in a behaviour chamber and avoided total residual oxidant (TRO) levels greater than 0·15-0·16 mg/litre. Cumulative exposures ranged from the equivalent of 0·38-5·23 in at 1·0/litre TRO. One day after exposure, routine oxygen consumption rates were decreased by 25 to 45% from pre-exposure rates and were correlated with the cumulative oxidant exposure. One month post exposure, respiration rates returned to pre-treatment levels. This transient depression of the respiratory rate did not affect survival or growth of chlorine-treated fish which were forced to compete with untreated conspecifics for a restricted food supply.  相似文献   

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