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Organochlorine residues and shell thicknesses in eggs of the clapper rail, common gallinule, purple gallinule, and limpkin (class Aves), eastern and southern United States, 1972-74.

Organochlorine residues and shell thicknesses were surveyed in eggs of the clapper rail (Rallus longirostris), purple gallinule (Porphyrula martinica), common gallinule (Gallinula chloropas), and limpkin (Aramus guarauna) from the eastern and southern United States. Clapper rail eggs were collected during 1972-73 in New Jersey, Virginia, and South Carolina. During 1973-74, gallinule eggs were collected in Florida, South Carolina, and Louisiana, and limpkin eggs were collected in Florida. Egg contents were analyzed for residues of organochlorine pesticides, including DDT, TDE, DDE, dieldrin, mirex, heptachlor epoxide, oxychlordane, cis-chlordane (and/or trans-nonachlor), cis-nonachlor, hexachlorobenzene (HCB), toxaphene, and endrin, and for polychlorinated biphenyls (PCBs). Shell thicknesses of recent eggs of these species were compared with archival eggs that had been collected before 1947. With the exception of the limpkin, the majority of eggs analyzed contained residues of p,p'-DDE and PCBs. Geometric means ranged from 0.10 ppm to 1.3 ppm. Small amounts (less than 1.0 ppm) of mirex, dieldrin, cis-chlordane (and/or trans-nonachlor), TDE, and DDT were detected in a few eggs. No evidence of eggshell thinning was found for any of the species studied. DDE residues in clapper rail eggs were higher in New Jersey and Virginia than in South Carolina.

Animals↗

Organochlorine residues and mortality of herons.

Since 1966, 72 herons found dead or moribund in the field have been analyzed for organochlorine chemicals. In addition, 36 herons were obtained through systematic collections, and carcasses were analyzed to determine sublethal exposure to organochlorines. Brains of birds found dead or moribund were analyzed to determine whether the birds had died of organochlorine poisoning. Residues of DDE were found most frequently (96 of 105 carcasses analyzed), PCBs were second (detected in 90 carcasses), and dieldrin and TDE (detected in 37 and 35 carcasses, respectively) were about equal as third and fourth most frequent. Endrin, mirex, toxaphene, and HCB were found least often (8, 9, 9, and 9 carcasses, respectively). At least one organochlorine was found in each carcass, except for six heron chicks found dead in a Maryland heronry. DDE and PCBs were present in highest concentrations; they exceeded 100 ppm in two birds each. Organochlorine concentrations were almost always higher in adult herons than in immature birds. All birds that had hazardous or lethal concentrations in the brain were adults, and most were great blue herons (Ardea herodias). Dieldrin was the chemical most often considered responsible for death. Herons died of suspected DDT and dieldrin poisoning years after the chemicals were banned in the United States. More than 20 percent of the herons found dead or moribund had lethal or hazardous concentrations of organochlorines in the brain.

Animals↗

Organochlorine residues in fish: National Pesticide Monitoring Program, 1970-74.

As part of the National Pesticide Monitoring Program, the U.S. Fish and Wildlife Service analyzed organochlorine contaminant residues in fish samples collected from about 100 stations each year from 1970 to 1974. During this period, mean residues of DDT and its metabolites declined nationally but remained widespread, and high concentrations continued to be present in areas where DDT use was extensive. Results of interlaboratory crosscheck analyses supported these conclusions, despite interpretation problems posed by intercompound analytical interferences in 1970 and 1971. Temporal trends in PCB residues were less obvious. Highest PCB residues were found in the industrialized areas of the Northwest and Midwest, and traces were present at most stations. Dieldrin and endrin residues remained essentially unchanged during this period; dieldrin residues were widespread and were highest in Hawaii and in areas of the Midwest where aldrin was used extensively. Toxaphene occurrence increased; it was formerly found only in fish from streams draining cotton-farming regions, but residues were detected in 1974 samples from other areas. According to the recommendation of the National Academy of Sciences' Water Quality Criteria, organochlorine residues in freshwater fish may have represented a hazard to piscivorous fish and wildlife at 71 percent of the stations sampled in 1970 and 66 percent in 1974.

Animals↗

Gas-liquid chromatographic determination of nonpolar organochlorine pesticide residues in a crude vegetable oil and its refinery by-products.

A crude soybean oil, several of its refinery by-products (described as soapstock, deodorizer distillate, and clabber stock), and the completely refined oil were analyzed for pesticide residues. Fourteen organo-chlorine pesticides and pesticide metabolites were found in the deodorizer distillate; 5 of these were also found in the clabber stock. Levels in these by-products ranged from 0.3 to 8 ppm. Only endrin and dieldrin were detected in the crude oil at levels of 0.01 and 0.05 ppm, respectively. Forty to 150 times these levels were found in the deodorizer distillate and clabber stock. Pesticide residues were not detected in the refined oil or in the soapstock at limits of detection for dieldrin of about 0.01 and 0.1 ppm, respectively. The method used by the Food and Drug Administration to analyze fats and oils for multiple organohalogen pesticide residues was inadequate for the extraction of pesticide residues from vegetable oil refinery by-products. The method used to analyze the crude vegetable oil and the refinery by-products involved dissolution of the oil samples in ethyl acetate-toluene, filtration if necessary, cleanup by gel permeation chromatography, and then Florisil column chromatography. The oil was isolated from aqueous-oil mixtures by extraction with hexane before analysis. The crude soybean oil was fortified with 12 organohalogen pesticides and Aroclor 1254 at levels of 0.5-3.7 ppm. Recoveries ranged from 83 to 102%.

Animal Feed↗

Extraction procedures for oilseeds and related high fat-low moisture products.

A combined sample preparation/extraction procedure is presented for pesticide residue analysis of oilseeds and related high fat-low moisture products. The procedure utilizes high-speed milling to prepare the sample and high-speed homogenization in the extraction step to achieve what is apparently quantitative isolation of both incurred residues and natural oils. A separate, simple, oil determination step allows findings to be reported on either the fat or whole product basis. Petroleum ether, ethyl ether-petroleum ether (1 + 1), and ethanol are used serially as the extractants. Usual fatty food cleanup procedures and multiresidue gas chromatographic detection techniques are utilized. The procedure presented in this paper is a refinement of earlier work which used a homogenizer both to grind and to extract samples of unground seeds and which demonstrated essentially complete extraction of endrin residues in soybeans and DDT residues in mustard seed. Identical samples analyzed by the currently recommended shakeout procedure, 29.012, gave recoveries of approximately 50% of the total residues. The procedure presented in this paper was satisfactorily tested on 13 different oilseed types and one sample of soda crackers. Oil content for these samples ranged from 5 to 69%.

Arachis↗

Inhibition of metabolic cooperation in Chinese hamster cells by organochlorine pesticides.

Effects of organochlorine pesticides on the metabolic cooperation in the hypoxanthine-guanine-phosphoribosyl-transferase system using wild-type 6-thioguanine-sensitive V79 cells and variant 6-thioguanine-resistant cells were surveyed. The metabolic cooperation was inhibited by 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane (DDT), 1,1-dichloro-2,2-bis(p-chlorophenyl)ethane (TDE), 1,1,1-trichloro-2-(o-chlorophenyl)-2-(p-chlorophenyl)ethane (o,p'-DDT), 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)ethane (methoxychlor), aldrin, dieldrin, endrin, heptachlor, alpha-isomer of benzene hexachloride (alpha-BHC), and gamma-BHC, but not beta-BHC. The present results suggest that the pesticides which inhibited the metabolic cooperation may be tumor promoters.

Animals↗

Pesticides in ground water beneath irrigated farmland in Nebraska, August 1978.

During the 1978 irrigation season, 14 ground water samples were collected in the Central Platte region of Nebraska, an area known to have high nitrate-nitrogen (NO3--N) levels, and analyzed for the presence of 13 pesticide residues. Atrazine levels ranged from 0.06 microgram/liter to 3.12 microgram/liter and were correlated to NO3--N concentrations with a coefficient of r = +0.55. Nitrate-nitrogen concentrations were measured as indicators of deep percolation from irrigated lands and ranged from 17.1 mg/liter to 34.3 mg/liter. Alachlor levels ranged from less than 0.01 microgram/liter to 0.71 microgram/liter. The amounts of 2,4-D were indeterminate because of experimental problems. Levels of the herbicides silvex and EPTC were below the limits of detectability. Levels of the organochlorine insecticides endrin, gamma-BHC (lindane), dieldrin, DDT and its primary metabolite DDE, heptachlor and its primary derivative heptachlor epoxide, and methoxychlor were all below the detectable limits of 0.005-0.010 microgram/liter.

2,4-Dichlorophenoxyacetic Acid↗

Organochlorines, cholinesterase inhibitors, and aromatic amines in Dutch water samples, September 1969--December 1975.

The Dutch aquatic environment was monitored from September 1969 to December 1975 for organochlorine pesticides and their metabolites, cholinesterase inhibitors, and aromatic amines. The 1,492 samples analyzed included surface water, rainwater, groundwater, and drinking water. The highest concentrations of hexachlorobenzene (HCB) and alpha- and beta-benzene hexachloride (BHC) were found in the Rhine River and its tributaries. Concentrations of the compounds in the Dutch part of the Rhine River decreased downstream. Other organochlorine pesticides and their metabolites, heptachlor, heptachlor epoxide, aldrin, dieldrin, endrin alpha- and beta-endosulfan, and sigmaDDT were detected occasionally, but only in low concentrations. Cholinesterase inhibitors and aromatic amines were always present in the Rhine River and its tributaries.

Amines↗

Organochlorine pesticide levels in Ottawa drinking water, 1976.

Duplicate samples of Ottawa drinking water were collected once a month during 1976 and analyzed for organochlorine pesticides. The samples were analyzed by gas chromatography--mass spectrometry, and pesticides were identified by comparing their retention times, coupled with selected ion monitoring, with those of known standards. The pesticides detected and their mean concentrations in parts per trillion were aldrin (0.9), heptachlor epoxide (3), heptachlor (0.6), alpha-BHC (6), gamma-BHC (3), endrin (4), dieldrin (1), o,p'-TDE (1), o.p'-DDT (3), and o,p'-DDE (0.2).

Hydrocarbons, Chlorinated↗

Residual concentrations of propanil, TCAB, and other pesticides in rice-growing of soils in the United States, 1972.

Ninety-nine soil samples from the rice-growing states of Arkansas, California, Louisiana, Mississippi, and Texas were collected, primarily to monitor the herbicide propanil. No residual concentrations of propanil were detected in any of these samples, but TCAB, a propanil transformation product, was detected in six samples at concentrations ranging from 0.01 ppm to 0.05 ppm. Organochlorine and organphosphorus pesticide determinations were also performed. The compounds dieldrin, aldrin, and DDT and its metabolites were found more frequently; endrin and chlordane were found less frequently. The organophosphorus pesticides diazinon and parathion were detected occasionally.

Anilides↗

Organochlorine residues in fish of Lake Texoma, October 1979.

Fillets from 99 fish, representing 11 species and three areas within Lake Texoma, were examined for residues of common organochlorines. Statistical analyses were conducted to determine the relationship of residues in fish fillets to trophic level and to geographical location of the sample. Most species contained PCBs at levels up to 100 ng/g and p,p'-DDE as high as 127 ng/g. p,p'-TDE and o,p'-DDT were not found in carnivores, but were present in herbivores and detritivores in amounts up to 36 ng p,p'-TDE/g and 17 ng o,p'-DDT/g. Heptachlor also was not found in carnivores, but was present as high as 37 ng/g in the other two classes. Chlordane ranged to 24 ng/g and was detected in all trophic levels. Dieldrin and p,p'-DDT were present in detritivores and carnivores up to 144 ng dieldrin/g and 410 ng p,p'-DDT/g. Neither substance was found in herbivores. Mirex, endrin, and heptachlor epoxide were present only at low levels. Statistically significant differences (P = 0.05) were found between trophic levels for seven of the eleven organochlorine compounds. No correlation (P = 0.05) was found between fillet concentrations of any parameter and geographical location of the sample.

Animals↗

Determination of organochlorine pesticides in cheese.

A multiresidue technique was developed for the analysis of 17 organochlorine compounds in cheese: alpha-hexachlorocyclohexane (alpha-HCH), beta-HCH, gamma-HCH, delta-HCH, aldrin, dieldrin, endrin, heptachlor, heptachlor epoxide, chlordane, o,p'- ... (o,p'-DDT), p,p'-DDT, o,p'- ... (o,p'-DDD), p,p'-DDD, o,p'- ... (o,p'-DDE), p,p'-DDE, and the fungicide hexachlorobenzene. In this technique, the fat, previously extracted from the cheeses, was subjected to 2 cleanup and extraction methods: with H2SO4, for acid-resistant organochlorine pesticides, and with KOH-ethanol. The behavior of the compounds in both treatments enabled us to identify the organochlorine pesticides in cheese. The precision (repeatability and reproducibility) and accuracy of the technique were validated.

Animals↗

Organochlorine insecticide residues in African Fauna: 1971-1995.

Organochlorine insecticides (OCLs), which were introduced in the decade following World War II, were used extensively in Europe, the U.S., and other developed countries into the 1970s. However, data began to accumulate on their persistence in soils and aquatic sediments, their potential to be taken up into animal tissues and to bioconcentrate in birds and mammals in the higher tropic levels of food chains and even in humans. As a result, registration authorities phased out their use progressively, in Europe and the U.S., from 1973 onward. However, the production of OCLs in developed countries and their use in developing countries continued through the 1970s and 1980s into the 1990s because they were, no longer under patent agreement, were inexpensive to manufacture, and were very effective in pest control. In Africa, the use of OCLs continued well into the 1990s for the control of mosquitoes, tsetse flies, and desert locusts as well as to combat various crop, animal, and human pests. Some of these uses involved extensive spraying of large areas of nonagricultural land, thereby exposing many groups and species of wildlife to their residues. Although there is some evidence of a gradual decline in the use of OCLs in Africa, they are still being used in appreciable quantities. During the past 25 yr, there have been 50 published reports of OCL residues in the various groups of invertebrate and vertebrate animals constituting the African fauna. These have been based on a diverse range of surveys, target animals, sampling methods, and analytical techniques. Moreover, they are extremely regionally-biased, the most intense surveys being in Zimbabwe, Kenya, Egypt, and South Africa. DDT was the most commonly used OCL, accounting for about half the total use, followed closely by dieldrin and HCH. Birds and fish have been sampled most intensively, with relatively few studies on other taxa. We reviewed the OCL residue data on African fauna from these reports and summarized the maximum and mean residues in the various groups of terrestrial and aquatic invertebrates and vertebrates. Overall, residues in the fauna were the greatest for DDT, followed in turn by those of dieldrin, HCH, endosulfan, and endrin, with small amounts of aldrin and toxaphene being found in some animals. There were relatively few reports of OCL residues in terrestrial invertebrates and virtually none in aquatic invertebrates. Only a few reports demonstrated OCL residues in terrestrial vertebrates, although high levels of DDT, dieldrin, and HCH were found in crocodile eggs and large residues of dieldrin occurred in bats, squirrels, and monkeys. Considerable OCL residues were reported in a few species of fish, especially Barbus, Clarias, Hydrocynus, Labeo, Sarotherodon, Epiplatys, and Synodontis. These residues were at levels that could have caused chronic toxicity or behavioral changes. The calculated maximum and mean OCL residues in the various elements of the African fauna until 1995 were compared with those calculated for corresponding faunal groups in Europe and the U.S. from their development and introduction up to 1973. The OCL residues reported in African fauna between 1971 and 1975 tended to be significantly higher overall than those published for Europe and the U.S. In particular, residues of DDT and dieldrin in African birds and their eggs were greater than those that had been incriminated as causing significant eggshell thinning and reproductive failure in European and U.S. aquatic and terrestrial birds up to 1973. Additionally, high DDT and dieldrin residues were reported from some species of African fish at levels that could potentially affect their reproduction, have chronic toxic and behavioral effects, and even drastically affect populations. Holistic case studies on the use of OCLs to control tsetse flies and desert locusts were discussed. OCL levels in trophic levels of fauna associated with Lake Kariba (between Zambia and Zimbabwe) were summarized. (AB

Africa↗

The debate on DDT.

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Adipose Tissue↗