An eleven-year study of chlorinated hydrocarbon insecticide residues in bovine fat in Illinois, 1972-1982

Bovine fat samples in Illinois were monitored for residues of chlorinated hydrocarbon insecticides from 1972 through 1982. The percentage of fat samples that were contaminated with all chlorinated hydrocarbons decreased during the 11-year study. The percentage of samples contaminated with DDT and its analogs decreased most markedly from 82.4% in 1972 to 2.1% in 1982. The percentage of samples contaminated with aldrin/dieldrin and heptachlor/heptachlor epoxide began to decline in 1980 and continued to decrease through 1982.     

Residues of chlorinated hydrocarbon insecticides in human milk of Jordanian women

A total of 411 milk samples were screened for the residues of the following chlorinated hydrocarbon insecticides using chromatographic methods: DDT insecticides (P,P'-DDT, P,P'-DDE, P,P'-DDD, O,P' -DDT); cyclodiene insecticides (aldrin, endrin, dieldrin, heptachlor, heptachlorepoxide, cis-and trans-chlordane); hexachlorocyclohexane (alpha-HCH, gamma-HCH) and hexachlorobenzene (HCB). The milk samples were obtained from lactating women selected randomly from five different geographical regions in Jordan. These regions were North and Middle Jordan Valley, Amman, Irbid and Zarqa. All of the studied insecticides were found to contaminate human milk in Jordan, but with high variations in the concentration and percentage of population occurrence. P,P'-DDE was the predominant contaminant occurring in 80.3% of studied population, followed by P,P'-DDT occurring in 53.5%. The regional results showed that the DDT residues were also the predominant contaminant in all regions and that the North and Middle Jordan Valley regions were the most affected. Infant's age (i.e. lactation period) had a significant inverse relationship with the concentration of insecticides in the milk fat.     

Trends in the levels of some chlorinated hydrocarbon residues in adipose tissue of Canadians

Trends in the levels of hexachlorobenzene, hexachlorocyclohexanes, oxychlordane, t-nonachlor, heptachlor epoxide, dieldrin, DDTs and polychlorinated biphenyls in adipose tissue of the Canadian population were followed from 1969 to 1985. Residues of lindane, dieldrin and p,p'-DDT continuously and significantly (P<0.025) decreased during that time, coinciding with restrictions on their use. Other residues also decreased significantly between 1969 and 1985, although not always continuously, while t-nonachlor levels did not change significantly since 1972. In general no consistent and/or significant differences were observed between the sexes, but in some instances differences were found for a particular residue in a given year. Three arbitrarily chosen age groups (0-25; 26-50 and > or =51 years) showed a downward trend in residue levels with time. The results of the surveys also indicate an increase in adipose tissue burden of chlorinated hydrocarbons with age, but this increase became apparently less significant with increasing age.     

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.     

Temporal changes in some chlorinated hydrocarbon residue levels of Canadian breast milk and infant exposure

Between 1967 and 1986, five national surveys were carried out to determine organochlorine residues in Canadian breast milk. In these surveys the number of samples, their geographic sampling distribution and fat content changed over the years. In addition, the number of samples obtained from younger mothers decreased, while those from older mothers (31-40 years) increased. Total DDTs showed the most consistent decline of all declining residues, while PCBs only decreased after 1982. Levels of oxychlordane and trans-nonachlor remained constant. Ratios of p,p'-DDE/p,p'-DDT gradually increased from 3.1 to 10.0 over the same period of time. With few exceptions, regional trends in residue levels followed those observed for the whole country. Although the number of reported chemicals increased since 1967, this was not necessarily reflected in the total accumulated residues in breast milk. By 1986, the daily intakes of all compounds at 8 weeks of nursing were well below the established acceptable daily intakes.     

Bald eagle mortality and chlorinated hydrocarbon contaminants in livers from British Columbia, Canada, 1989-1994

Between 1989 and 1994, we obtained 278 carcasses of bald eagles (Haliaeetus leucocephalus) found dead or dying in British Columbia, Canada. All specimens were necropsied and the cause of death determined wherever possible. Livers from a subset of 75 birds were analyzed for polychlorinated biphenyl (PCB) and organochlorine (OC) pesticide residues. A further subset of 19 eagles found dead around the Strait of Georgia, an area of known pulp mill pollution, in summer, and therefore presumably resident birds, were analyzed for polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) and non-ortho PCBs. Liver concentrations ranged from less than 1 to 190 mg/kg for DDE, and up to 72 mg/kg for total PCBs. Concentrations of other OCs were generally less than 1 mg/kg, with the exception of chlordane-related compounds which were occasionally over 2 mg/kg. All birds analyzed for PCDDs and PCDFs contained detectable concentrations of the major 2,3,7,8-substituted isomers. Some birds were very contaminated; one eagle found near a kraft pulp mill site in 1990 contained: 400 ng/kg 2,3,7,8-TCDD, 1400 ng/kg 1,2,3,7,8-PnCDD and 4400 ng/kg 1,2,3,6,7,8-HxCDD. Birds with higher PCB and dichlorodiphenyldichloroethane (DDE) concentrations appeared to weigh less, and there was a significant negative relationship between both PCBs and DDE and numeric scoring of body condition, reflecting the well known process of starvation-induced mobilization of body lipids and contaminants. Birds with higher 2,3,7,8-TCDD concentrations tended to have unusually low concentrations of 2,3,7,8-TCDF, interpreted to indicate hepatic cytochrome P4501A-type induction by TCDD and subsequent metabolism of TCDF.     

Accumulation of chlorinated hydrocarbon vapours in pine needles

Needles with different ages from four pines have been analysed for PCB's, HCB, α- and γ-HCH, p,p'DDT and DDE. The accumulation found has been discussed and provisional accumulation rates under actual background conditions have been calculated.     

Determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by liquid chromatography-tandem mass spectrometry

A sensitive method for determination of chloramphenicol, enrofloxacin and 29 pesticides residues in bovine milk by high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) was developed. Residues of the targets were extracted from milk with acetonitrile, cleaned up by C₁₈-SPE cartridge, and then determined by HPLC-MS/MS. The MS detection was operated in positive or negative ionization mode, depending on the compounds. For confirmation of each target compound, two precursor ion > product ion transitions were selected by multi-reaction monitoring mode (MRM). The method showed good linearity for all the tested compounds over the studied concentration range with correlation coefficient higher than 0.9910. Recoveries for the studied compounds at three spiked levels (0.05, 0.10, 0.19 mg kg⁻¹) in bovine milk were in the range of 71-107% with RSDs not larger than 13.7%, except that recoveries of trifluralin ranged between 62% and 70% at the spiked levels. Limits of quantitation for the analytes were estimated to range between 0.03 × 10⁻³ and 14.5 × 10⁻³ mg kg⁻¹. The proposed method was applied for the determination of the analytes residues in real samples. The found levels of the analytes in milk samples were lower than maximum residues levels (MRL).     

Dry aerial fallout of organochlorine insecticide residues in Delhi, India

Monitoring of airborne dust in Delhi during May to July 1985 revealed residues of DDT varying from 1.3 to 7.14 ng mg(-1) (4.06-22.31 ng m(-2) day(-1)) with an average of 3.32 ng mg(-1) (10.38 ng m(-2) day(-1)), and HCH which ranged from 0.46 to 2.35 ng mg(-1) (1.44-7.34 ng m(-2) day(-1)) with a mean of 1.16 ng mg(-1) (3.63 ng m(-2) day(-1)). The concentration of total DDT was almost 3 times greater than that of HCH.     

Dieldrin, heptachlor, and chlordane residues in soybeans in Illinois 1974, 1980

The Illinois soybean crop was monitored in 1974 and 1980 for dieldrin, heptachlor, and chlordane residues resulting from the use of these compounds for corn soil insect control in the years before extensive soybean cultivation. Residue levels were compared with past published amounts. Dieldrin residue levels in soybeans declined between 1974 and 1980. Heptachlor and heptachlor epoxide levels remained level between 1974 and 1980. Chlorinated hydrocarbon residues were lower in the southern third of Illinois than for the remainder of the state.     

Induction of aryl hydrocarbon hydroxylase by chlorinated dibenzofurans in rats

Five of 25 chlorinated dibenzofurans induced aryl hydrocarbon hydroxylase in rats when administered orally at 40 μg/kg body weight. Active inducers included the three congeners with chlorines in all four lateral positions and the 2,7- and 2,8-dichlorodibenzofurans. The findings agree well with other studies involving common congeners, but do not agree with findings in that congeners with three lateral chlorines were inactive .     

Heterogeneity of chlorinated hydrocarbon sorption properties in a sandy aquifer

Hydraulic conductivity and sorption coefficients for chlorinated hydrocarbons (chloroform, carbon tetrachloride and tetrachloroethylene) were evaluated for 216 sediment samples collected across a 15 m transect and a 21 m depth interval in a contaminated aquifer near Schoolcraft, Michigan. Relationships between hydraulic conductivity, linear sorption partition coefficients, grain size classes, and spatial location were investigated using linear regression analysis and geostatistical techniques. Clear evidence of layering was found in sorption properties, hydraulic conductivity and grain sizes. Conductivity correlated well with grain size, as expected, but sorption varied inversely with grain size, contrary to some previous reports. No significant correlation was found between sorption properties and hydraulic conductivity. This is likely due to the unexpected presence of small amounts of highly sorptive coal-like solids, which dominate the sorption behavior but have little effect on conductivity. The results demonstrate that recent findings regarding the high sorption capacity of coal materials found in soils can exert a controlling influence on contaminant transport. Designers of in situ remediation systems should be cautioned that 1) it is not reasonable to assume that sorption capacity and hydraulic conductivity are related, 2) sorption capacity and hydraulic conductivity are critical measurements for contaminant site characterization and subsequent transport modeling, 3) estimating sorption capacity from organic carbon measurement may lead to greater errors than performing sorption isotherms, and 4) it is more important to characterize vertical heterogeneity rather than horizontal heterogeneity because both sorption and hydraulic conductivity are correlated across longer distances in the horizontal plane.     

Remediation of a chlorinated aromatic hydrocarbon in water by photoelectrocatalysis

Photoelectrocatalysis driven by visible light offers a new and potentially powerful technology for the remediation of water contaminated by organo-xenobiotics. In this study, the performance of a visible light-driven photoelectrocatalytic (PEC) batch reactor, applying a tungsten trioxide (WO₃) photoelectrode, to degrade the model pollutant 2,4-dichlorophenol (2,4-DCP) was monitored both by toxicological assessment (biosensing) and chemical analysis. The bacterial biosensor used to assess the presence of toxicity of the parent molecule and its breakdown products was a multicopy plasmid lux-marked E. coli HB101 pUCD607. The bacterial biosensor traced the removal of 2,4-DCP, and in some case, its toxicity response suggests the identification of transient toxic intermediates. The loss of the parent molecule, 2,4-DCP determined by HPLC, corresponded to the recorded photocurrents. Photoelectrocatalysis offers considerable potential for the remediation of chlorinated hydrocarbons, and that the biosensor based toxicity results identified likely compatibility of this technology with conventional, biological wastewater treatment.     

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 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.     

Seasonal variations of organochlorine insecticide residues in air from Porto Novo, South India

Air samples collected from Porto Novo (11 degrees 29' N, 79 degrees 46' E), Tamil Nadu State, South India from December, 1987 to January, 1989 were analysed to determine the seasonal variations of the levels of organochlorine insecticides such as HCH (BHC) and DDT. Both these insecticides showed higher levels from August to January, although this trend was more marked in HCH than DDT, reflecting the application of HCH largely, and probably small quantities of DDT during the flowering season of rice. The alpha-HCH was detected as a dominant isomer for all seasons monitored followed by gamma-HCH. Among DDT compounds, p,p'-DDT was the highest except in dry season (January to April) when p,p-DDE showed higher percentage. The levels and percentage composition of these insecticides recorded in the present study may aid in interpreting the role of a 'point source' area since India is one of the countries still using the persistent organochlorine pesticides in large quantities.     

Contamination of bovine milk with DDT and HCH residues in relation to their usage in malaria control programme

The contribution of spraying DDT and HCH for malaria control towards the contamination of bovine milk was investigated by analysing milk samples collected from preselected localities sprayed with either DDT or HCH in the Punjab. A direct correlation was found between the amounts of residues of these insecticides in milk and their typical usage pattern for the mosquito control programme. It is considered that these results may have significant bearing on the regulatory control of DDT and HCH residues in milk.     

Screening of antibiotic residues in fresh milk of Kathmandu Valley,Nepal

The prevalence of two groups of antibiotics; namely penicillin and sulfonamides was studied in fresh milk available in Kathmandu Valley of Nepal. The milk samples (n = 140) were collected from three different sources; individual farmers, cottage dairies and organized dairies of Kathmandu valley. Qualitative and semi-quantitative analysis with rapid screening kits revealed that 23% samples were positive for antibiotic residues in the fresh milk for penicillin and sulfonamide groups (1–256 µg/kg). High performance liquid chromatography (HPLC) analyses detected 81% samples positive for amoxicillin (68–802 µg/kg), 41% for sulfadimethoxine (31–69 µg/kg), 27% for penicillin G (13–353 µg/kg), and 12% for ampicillin (0.5–92 µg/kg). Due to the precision and accuracy of liquid chromatography method, it detected more positive samples and consequently presented higher prevalence than the rapid screening kits. The antibiotic residues were found above the maximum residue limits that presented serious threat to consumer health and raised a serious concern regarding the implementation and monitoring of international regulations in developing countries.     

MIP系统在某挥发性氯代烃污染地块调查中的应用

针对我国挥发性有机污染地块调查评估中存在的采样缺失、成本高及周期长等问题,选择华北地区某挥发性氯代烃污染地块为研究对象,采用现行调查方法与基于膜界面探针(MIP)系统快速调查技术联合使用的方式,现场完成场地钻探调查点位4个(土壤样品36个),MIP系统调查点位11个(验证点位4个),以研究MIP验证点位检测电信号值与其对应场地钻探点位的地层信息、实验室检测数据之间的相关性,以及使用MIP电信号值模拟地块地层和污染空间的分布特征。结果表明,MIP系统检测的土壤电导率电信号值(EC)能够更为详尽地表征地块的地层结构信息;在地块范围内的同一种土质中,MIP系统的专用卤素检测器电信号值(XSD)与实验室检测数据拟合度相对较高(R²>0.99);MIP系统快速调查技术与现行调查方法联合使用能够快速且高效表征调查地块内VCHs的污染空间分布特征。本研究结果可为MIP系统快速调查技术在挥发性有机污染地块调查评估中的应用提供参考。     

碱活化过硫酸盐在某氯代烃污染场地地下水修复中的应用

碱活化过硫酸盐适用于降解污染土壤及地下水中的氯代烃。以典型氯代烃类污染场地为研究对象,开展了碱活化过硫酸盐降解地下水中氯代烃的小试实验研究及中试规模工程应用。结果表明：污染物去除率与污染物初始浓度、氧化剂投加比相关;污染物初始浓度越高,去除率越低;氧化剂投加量越大,去除率越高,用于该场地地下水修复的最佳氧化剂投加比为1%~3%。中试药剂原位注入采用高压旋喷注射工艺,按最佳氧化剂投加比将药剂注入至污染含水层,跟踪监测结果表明：经注药修复8个月后,地下水中氯代烃污染物浓度明显下降,大部分区域的污染物浓度已达到修复目标,局部初始浓度偏高区域的污染物浓度接近修复目标。同时,对氧化剂产物残留$ {\rm{S}}{{\rm{O}}^{2 - }_4}$浓度进行监测发现：$ {\rm{S}}{{\rm{O}}^{2 - }_4}$浓度随修复后时间延长逐渐降低,通过趋势分析预测的残留$ {\rm{S}}{{\rm{O}}^{2 - }_4}$浓度将逐步下降直至恢复正常水平或满足相关标准。