Organochlorine residues in shellfish from Maryland waters, 1976-1980

Shellfish samples, including the American oyster (Craessostrea virginica), the soft shell clam (Mya arenaria), the hard shell clam (Mercenaria mercenaria) and the blue crab (callinectes sapidus), were taken from the Maryland section of the Chesapeake Bay and its tributaries over a five year period (1976-80) and analyzed to determine residue levels of various organochlorine pesticides. Qualitative and quantitative information was obtained for a variety of polychlorinated hydrocarbons. The purpose of this study includes the establishment of baseline values for levels of shellfish contamination, utilization of the data as an indicator of probable levels of water and sediment contamination in the vicinity of the sampling site and ensurance that shellfish harvested for human consumption are within U.S. Food and Drug Administration guidelines for organochlorine contamination. All mean values and virtually all individual values were within FDA guidelines.     

Trace metal residues in shellfish from Maryland waters, 1976-1980

Levels of seven heavy metal residues, arsenic, cadmium, chromium, copper, lead, mercury and zinc were monitored in samples of the American oyster (Crassostrea virginica), the soft shell clam (Mya arenaria), the hard shell clam (Mercinaria mercinaria) and the blue crab (Callinectes sapidus). Samples were taken from the Maryland section of the Chesapeake Bay and its tributaries over a five year period (1976-80). This study was undertaken to provide an estimate of a baseline for values of trace heavy metals. Also, the oyster, being a non-mobile filter feeder, provides information regarding the level of metal residues in its environment (water and sediment), because heavy metal uptake is related to the surrounding metal concentrations. Additionally, this type of monitoring program is essential to ensure that shellfish sold for human consumption are within safe limits established for toxic substances by the United States Food and Drug Administration. Results of the study are consistent with data from previous years and no statistically significant year-to-year trends were observed over the period of the investigation.     

Trace metal residues in finfish from Maryland waters, 1978-1979

Levels of seven heavy metal residues, arsenic, cadmium, chromium, copper, lead, mercury and zinc were monitored in samples of various species of finfish harvested from the Maryland section of the Chesapeake Bay and its tributaries over a two year period (1978-79). Results of the analysis of the edible portions of these finfish are presented along with the species of finfish, date and location of harvest. A number of samples of finfish gonad and liver tissue were analyzed to study the relative level of preconcentration of heavy metals in these tissues compared to the edible (flesh) portion. Results of this study are consistent with other available data for Atlantic Coast finfish. Gonad tissue, when compared to flesh, show enrichment of copper and zinc and decreased mercury and cadmium levels. Liver tissue shows enrichment in copper, zinc and cadmium and generally lower levels of mercury compared to flesh.     

Organochlorine residues in harbour porpoises from Southwest Greenland

During the 1995 hunting season, 75 harbour porpoises (Phocoena phocoena) were sampled in three locations in West Greenland: Maniitsoq, Nuuk, and Paamiut. Sex, age, morphometrics, reproductive condition, and organochlorine compound (OC) levels in blubber were determined for each individual. OC levels were extremely low and, therefore considered unlikely to affect the population adversely: mean blubber concentrations, expressed on lipid weight basis were 1.98 (S.D.=1.1) mg/kg for PCBs, 2.76 (S.D.=1.66) mg/kg for tDDT and 0.21 (S.D.=0.11) mg/kg for HCB. No statistical differences were observed among individuals caught in the various locations. OC concentrations showed statistically significant positive associations with age in males but negative in females; consequently, mature females presented lower pollutant loads than their male counterparts. Juveniles did not show differences between sexes. A higher proportion of less chlorinated and more metabolizable polychlorinated biphenyls (PCBs) compared to tPCBs was found in calves (age< or =1) than in mature females, indicating that the feeding habits of these two groups differ and that a greater transfer of less chlorinated compounds is passed from females to their pups through lactation and parturition. Harbour porpoises significantly contribute to the dietary intake of OCs by local Inuit populations. This contribution could be reduced if mature males were selectively avoided; however, current hunting procedures make this selection impracticable.     

Organochlorine residues in odontocete species from the southeast coast of India

Blubber from bottle-nose dolphins, spinner dolphins, humpback dolphin (Tursiops truncatus, Stenella longirostris and Sousa chinensis) were collected from the Bay of Bengal (southeast coast of India) and analyzed for the organochlorine pesticides hexachlorocyclohexane (HCHs), p,p'-dichlorodiphenyl trichloroethane (DDTs), and polychlorinated biphenyls (PCBs). All nine specimens analyzed contained considerable levels of all the three chemical classes where DDT was in the range of 3330-23330 ng/g; HCHs in the range of 95-765 ng/g; and PCBs in the range of 210-1220 ng/g (wet weight basis). The reasons for this and the variations in the isomer pattern of HCHs and DDT and its metabolites in marine mammal tissues are discussed.     

Organochlorine concentrations in franciscana dolphins, Pontoporia blainvillei, from Brazilian waters

Blubber samples were collected from ten franciscana dolphins either incidentally captured in fishing operations or stranded on São Paulo (SP) and Paraná (PR) states littoral, Southeastern and Southern Brazilian coast, respectively. Determination of PCB, DDT and HCB concentrations were performed by capillary gas chromatograph coupled to electron capture detector (ECD). ΣDDT, ΣPCB and HCB concentrations ranged from 264 ng g⁻¹ to 5811 ng g⁻¹ lipid, from 909 ng g⁻¹ to 5849 ng g⁻¹ lipid and from 10 ng g⁻¹ to 61 ng g⁻¹ lipid, respectively. Regarding DDTs, the distribution of the mean percentages decreased in the following order: p,p′-DDE > p,p′-DDD > p,p′-DDT. The ΣDDT/ΣPCB ratio varied between 0.27 and 0.42 in Northern and Central SP coast, while in Southern SP and PR coast the values were 1.6 and 1.9, respectively. Dissimilarities in ΣDDT/ΣPCB ratios point to different sources of organochlorine compounds to franciscana dolphins in the study area. Considering the endocrine disruptive action of organochlorine compounds, the concentrations found in franciscana dolphins from Brazilian waters may represent an additional obstacle to the conservation of this endangered cetacean species.     

Organochlorine pesticide and polychlorinated biphenyl residues in foodstuffs from Bangkok, Thailand

Raw foodstuffs collected from Bangkok, Thailand, were analysed for the presence of PCBs, DDTs, HCHs (BHCs). HCB, aldrin, dieldrin, heptachlor and heptachlor epoxide. Residues of PCBs and organochlorine pesticides were detected in all the samples analysed. Concentrations of PCBs did not reach the tolerance limit set forth by the US Food and Drug Administration (FDA). The concentrations of SigmaHCH were higher than those of SigmaDDT in all the farm products while the levels of SigmaDDT were greater in fishes including fish flakes and fishmeal. Meat samples recorded higher concentrations of SigmaDDT and dieldrin than SigmaHCH. Comparing the levels of organochlorines in foodstuffs from Bangkok, considerable levels of aldrin and dieldrin indicate the need for concern from the food safety point of view because of their much higher toxicity than DDT and other organochlorines. However, the levels did not exceed the Maximum Residue Limit (MRL) recommended by FAO/WHO. Food contamination by HCB, heptachlor and heptachlor epoxide is comparatively lower.     

Organochlorine pesticide residues in sediments from the Uganda side of Lake Victoria

Organochlorine (OC) residues were analysed in 117 sediment samples collected from four bays of the Uganda side of Lake Victoria. The sediments were collected with a corer at a depth of 0-20 cm, and extracted for OC residues using a solid dispersion method. The extracts were cleaned using gel permeation chromatography and analysed for pesticide residues using a gas chromatograph (GC) equipped with an electron capture detector. The results were confirmed using a GC equipped with a mass spectrometer (MS). A total of 16 OC residues, most of them persistent organic pollutants (POPs) were identified and quantified. The OC residue levels were expressed on an oven dry weight (d.w.) basis. Endosulphan sulphate, in the range of 0.82-5.62 μg kg⁻¹d.w., was the most frequently detected residue. Aldrin and dieldrin were in the ranges of 0.22-15.96 and 0.94-7.18 μg kg⁻¹d.w., respectively. DDT and its metabolites lay between 0.11-3.59 for p,p′-DDE, 0.38-4.02 for p,p′-DDD, 0.04-1.46 for p,p′-DDT, 0.07-2.72 for o,p′-DDE and 0.01-1.63 μg kg⁻¹d.w. for o,p′-DDT. The levels of γ-HCH varied from 0.05 to 5.48 μg kg⁻¹d.w. Heptachlor was detected only once at a level of 0.81 μg kg⁻¹d.w., while its photo-oxidation product, heptachlor epoxide, ranged between non-detectable (ND) to 3.19 μg kg⁻¹d.w. Chlordane ranged from ND to 0.76 μg kg⁻¹d.w. Based on the threshold effect concentration (TEC) for fresh water ecosystems, aldrin and dieldrin were the only OCs that seemed to be a threat to the lake environment.     

Organochlorine residues in water from the Mahala water reservoir, Jaipur, India

Residues of p,p'-DDE, p,p'-DDT alpha-, beta-, gamma-isomers of HCH, aldrin and heptachlor in water, from four different sites of the Mahala water reservoir were monitored periodically from September 1985 to October 1987. All the samples contained the above residues in varying concentrations. Isomers of HCH predominated and were followed in relative dominance by aldrin, total DDT and heptachlor residues, p,p'-DDE and p,p'-DDD constituted the major fraction of total p,p'-DDT. Monthly total organochlorine residue levels in water ranged between 1.07 and 81.23 microg litre-1. The variation is attributed to the run-off or subsoil water movement from the catchment area.     

Organochlorine pesticides in the surface waters of Northern Greece

A survey undertaken in Northern Greece has shown that organochlorine pesticides are present in the surface waters. Surface water samples have been collected seasonally from four rivers and five lakes for a period of two years. Solid-phase extraction followed by gas chromatographic techniques with electron capture detection was used for the determination of the compounds. The most commonly encountered organochlorine pesticides in surface waters were the isomers of hexachlorocyclohexane, aldrin, dieldrin and endosulfan sulfate. In some cases the concentrations detected were higher than the qualitative target levels set by the European Union, especially for hexachlorocyclohexane and aldrin. The occurrence of these compounds in Greek surface waters can be attributed to intense agricultural activity as well as to transboundary pollution.     

Organochlorine insecticide residues in birds and fish from the Transvaal, South Africa

Fatty extracts of wild birds and fishes were analysed for certain organochlorine insecticides. Nearly all samples contained residues of one or more of the insecticides.     

Organochlorine pesticide residues and PCBs in eels ( ) from some British freshwater reedbeds

Organochlorine pesticide residues and PCBs were measured in bulked samples of whole eels collected in 1991 from 11 reedbed sites of wildlife conservation importance in Britain. Eels from some sites had only trace amounts of dieldrin, p,p-DDE and PCBs. Maximum concentrations were 0.21 mg kg⁻¹ for dieldrin, 0.27 mg kg⁻¹ for p,p-DDE and 0.91mg kg⁻¹ for PCBs (fresh weight). Concentrations of contaminants in eels from reedbeds were considered in general to be lower than in eels from rivers, but nevertheless concentrations were considered to be sufficiently high at some sites to adversely affect top carnivores such as the otter.     

Organochlorine pesticide residues in human milk in Punjab, India

Human milk samples collected from areas having intensive cotton cultivation and sparse cotton cultivation in Punjab (India) were analysed for organochlorine insecticides. Both DDT and HCH were detected in almost all the samples analysed. The average levels of Sigma-DDT and Sigma-HCH residues in samples from cotton-growing areas were significantly higher than in those from areas where cotton is sparsely grown. Residues of Sigma-DDT mainly comprised p,p'-DDT and p,p'-DDE, while those of Sigma-HCH residues were mainly in the form of its beta-isomer. Median values of 0.52 microg g(-1) of Sigma-DDT and 0.19 microg g(-1) of Sigma-HCH in samples of human milk from cotton-growing areas of Punjab (India) were higher than those reported from most other countries in the World.     

Organochlorine residues in roof timbers and possible implications for bats

In Britain, many species of bat regularly use buildings as roosts. DDT, DDE, dieldrin (HEOD) and gamma-HCH (lindane) have been detected in carcasses of bats that had died a short while before they were found. Roof timbers may be a source of this contamination. This study reports concentrations of organochlorines in (i) roof timbers known to have been treated in the past (spot samples; n - 17) and (ii) timbers before and after treatment with commercial permethrin formulations (pre-treatment and post-treatment samples, n = 11). Gamma-HCH was detected in 13 spot samples and HEOD in 6. Where present, mean (+/-1 SE) concentrations in wood were 15.6+/-6.5 microg g-1 WW (n = 13) and 25.0+/-11.8 microg g-1 WW (n = 6), respectively. DDT was not detected in any spot samples, but permethrin was detected in four (1264+/-567 microg g(-1) WW) samples, but not in the corresponding pre-treatment samples; in one other pair of samples, concentrations of gamma-HCH increased from 74 to 2468 microg g-1 WW after treatment. Both DDT and HEOD occurred in low (<2 microg g-1 WW) concentrations in five post-treatment samples and in one and zero pre-treatment samples, respectively; the highest dieldrin concentration measured was 30.9 microg g-1 WW. Permethrin was not detectable in any pre-treatment samples but was present in ten post-treatment samples in concentrations ranging from 93 to 2995 microg g-1 WW. The spot results suggest that low concentrations of organochlorines can persist in treated roof timbers for at least 13 years post-treatment. Occasionally, these pesticide residues in timber may be of sufficient magnitude to result in bats absorbing a substantial proportion of a lethal dose. Results also suggest that there is organochlorine contamination of permethrin formulations and that the solvents used in new applications of pesticide may re-mobilise organochlorines already present in wood.     

Organochlorine compounds in common dolphins (Delphinus delphis) from the Atlantic and Mediterranean waters of Spain

Blubber of free-ranging common dolphins (Delphinus delphis) from the northwestern coast of Spain (Atlantic), sampled in 1984 and 1996, and of common dolphins entangled in fishing nets in the southwestern Mediterranean, sampled during 1992 1994, was analysed for organochlorine pollutants. In the Atlantic, concentration of all pollutants was significantly higher in males than in females. The overall tPCB/tDDT ratio in this area was 3.35, which indicates a predominance of industrial inputs over those associated with agriculture. Individuals sampled in 1996 showed significantly lower DDT concentrations but a higher ppDDE/tDDT ratio than those sampled in 1984, which reflects the aging of the environmental load. In the same period, tPCB concentration remained constant and, as a consequence, the tPCB/tDDT ratio more than doubled. In the Mediterranean, the reduced sample size of adult individuals precluded proper statistical investigation of sex-related variation. The overall tPCB/tDDT ratio was 1.12, suggesting a higher contribution of pollutants of agricultural origin. Individuals had significantly higher levels of all DDT forms and a higher ppDDE/tDDT ratio than their counterparts from the Atlantic, but similar PCB concentrations. However, the relative frequency of the different congeners in relation to the total PCB load was different in the two areas. This indicates that the two populations do not mix, at least in the short- or medium-term. Organochlorine levels in both areas are at the mid to low end of the range of concentrations detected in other common dolphin populations and in that of other Delphinidae species from the same region. Although the impact of the organochlorine concentrations on the common dolphin populations surveyed cannot be assessed, it is considered unlikely that they have played a significant role in the decline that the species has suffered in recent decades in the western Mediterranean.     

Organochlorine insecticide residues in human fat and milk samples in South Africa

Samples of human fat and milk were analysed for the presence of organochlorine insecticides. The levels of these compounds in human samples declined significantly from 1973 to 1982.     

Organochlorine residues (PCBs and DDTs) in two Torpedinid species liver from the Southeastern Mediterranean Sea

Purpose  

Polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane (DDT) and PCB congeners accumulation profile were measured in the liver of two torpedinid species (Torpedo nobiliana and Torpedo marmorata) from the Mediterranean Sea (Adriatic Sea) in order to investigate the relative toxicological impact of these highly toxic PCBs in the organisms in question.     

Organochlorine and organophosphorus pesticide residues in the Atoya river basin, Chinandega, Nicaragua

The hydrographic basin of the Atoya river, located in the Department of Chinandega, one of the main cotton producing regions in Nicaragua, is intensively contaminated by pesticides. Samples of river waters and sediments, as well as strategically selected wells have been analyzed to study variations in the concentrations of organochlorine and organophosphorus pesticide residues between the dry season (November-April) and the rainy season (May-June). Generally, higher concentrations of pesticides have been detected in the river waters and sediments in the dry season. DDT, DDD, DDE compounds and toxaphene are the most frequent organochlorine residues found in the water and sediment samples, while endrin, aldrin, dieldrin and lindane are mainly found in the waters of rivers and wells. Organophosphorus compounds were rarely detected. However, residues of ethion, methyl-parathion and ethyl-parathion were found in high concentrations in some river and well water samples. Generally, organochlorine compounds tend to accumulate in the fine grain-size fractions, rich in organic matter, except DDE, which concentrates basically in the coarse grain-size fractions.     

Organochlorine and butyltin residues in walleye pollock (Theragra chalcogramma) from Bering Sea, Gulf of Alaska and Japan Sea

Persistent organochlorine (OC) and toxic butyltin compounds (BTs) were determined in walleye pollock (Theragra chalcogramma) collected from Gulf of Alaska, Bering Sea and Japan Sea, during 1991 and 1992. Polychlorinated biphenyls (PCBs) and dichlorodiphenyltrichloroethane (DDTs) and its metabolites were the most abundant compounds ranging up to 3200 and 2500 ng/g on lipid weight, respectively, followed by chlordane compounds (CHLs), hexachlorocyclohexane isomers (HCHs) and hexachlorobenzene (HCB) in the liver of walleye pollock. Concentrations of HCHs and HCB in walleye pollock from these remote areas were higher than those in fishes from the western North Pacific and Japanese coastal waters, indicating atmospheric transport of these compounds to higher latitude regions such as Bering Sea and Gulf of Alaska and/or local input around northern Japan Sea. The concentrations of other OCs were generally comparable to those in fishes from North Pacific Ocean and Japanese waters but significantly lower than in cod-like fishes from North Atlantic and European countries. Among sampling locations, walleye pollock from Japan Sea showed higher concentrations of DDTs and HCHs compared to fishes from Bering Sea and Gulf of Alaska, suggesting greater input of these compounds around Japan Sea. Slower declining trend of DDTs and CHLs and an increasing pattern of PCBs concentrations were found in walleye pollock from Bering Sea during 1982-1992. This may imply a continuous input of these compounds by long-range transport and/or long-term persistency in these cold regions. Compared to the fishes from Japan Sea, walleye pollock from Bering Sea and Gulf of Alaska showed higher proportions of alpha-HCH and p,p'-DDE in the composition of HCH isomers and DDT compounds, respectively. This suggests selective transportability of these compounds during long-range transport to higher latitude remote areas. Concentrations of tributyltin (TBT) in the muscle of walleye pollock ranged from 1.1 to 5.5 ng/g on wet weight. Concentrations of TBT in deep-sea walleye pollock from Gulf of Alaska and Bering Sea were lower than those in Japan Sea.     

Organochlorine pesticide residue and PCBs in harbour porpoise (Phocoena phocoena) incidentally caught in Scandinavian waters

During Norwegian and Danish harbour porpoise projects 1987-1991, subcutaneous blubber samples of 34 male harbour porpoises (Phocoena phocoena) were collected. Animals from three geographical locations, ranging from 56 degrees N, 12 degrees E to 71 degrees N, 26 degrees E, were chosen in order to study the organochlorine (OC) contamination in this species inhabiting the northeastern part of the North Atlantic Ocean, the northern North Sea and Kattegat, at the locations of Tufjord, Vestlandet and Gilleleje, respectively. Analytical standards used consisted of the industrial chemicals PCBs (22 individual PCB congeners and 6 industrial mixtures which contained 104 PCB congeners or group of congeners) and HCB, and the organochlorine pesticides DDT, HCH, the cyclodienes endrin, dieldrin and the chlordane metabolites oxychlordane and trans-nonachlor, and heptachlor epoxide. A total of 16 PCB congeners or groups of congeners, all the DDT metabolites except o,p'-DDD, and all the pesticides were detected in all animals. The concentrations of sigmaPCB (sum of concentrations of 47 detected PCB congeners) and sigmaDDT (sum of concentrations of all DDT detected compounds) ranged from 3.7-65.3 and 3.2-45.0 microg g(-1) lipid weight, respectively. The range of mean concentrations of dieldrin, endrin and trans-nonachlor was 1-3 microg g(-1), while mean concentrations of HCHs, heptachlor epoxide, and HCB were <1 microg g(-1). No significant variation in PCB congener pattern was apparent between geographical areas. The major PCB congeners nos 147/123, 153, 138/163/164, 182/187 and 180 at Gilleleje, Vestlandet and Tufjord represented 53%, 45% and 44% of sigmaPCB, respectively. A significant difference was found between the number of PCB congeners in blubber of newborn and older porpoises. This might indicate the presence of a blood/placenta barrier and/or selective mammary transport of PCBs with specific structures. A significant OC accumulation with age was apparent, with the exception of HCB and HCHs. Geographical differences in the levels of OCs were apparent for all compounds except for dieldrin and heptachlor epoxide. Significantly higher levels of chlordane metabolites (trans-nonachlor and oxychlordane) and endrin were found in the group of animals from the northern location Tufjord, while sigmaDDT, p,p'-DDTs, HCHs and PCBs were highest in the group of animals from the southern location Gilleleje. Highest levels of the o,p'-substituted DDTs were found in specimens from the middle location Vestlandet. These findings indicate little or no regular migration of harbour porpoise between these three locations. No correlations were found between OC concentrations and blubber thickness. Although mean values of sigmaDDT and sigmaPCB were in the lower end of previously reported levels in harbour porpoise from adjacent waters in the eastern part of the North Atlantic Ocean and along the coasts of North America, these levels are relatively high. The organochlorine concentrations in harbour porpoises in the present study were 2-3 times higher than corresponding OC levels detected in harbour seals (Phoca vitulina) from the same areas.