Organochlorine and mercury contamination of little terns (Sterna albifrons) breeding at the western Baltic Sea, 1978-96

Between 1978 and 1996, egg and chick samples of little terns (Sterna albifrons) breeding at different colony sites along the eastern coast of Schleswig-Holstein, Germany, were annually gathered by chance in the framework of a long-term ringing programme. Analyses of polychlorinated biphenyls (PCBs), dichlorodiphenyltrichloroethane (DDT), hexachlorobenzene (HCB), hexachlorocyclohexane (HCHs), and mercury were carried out on eggs, chicks, and down (only mercury). In all matrices, pollutant concentrations decreased over the 19-year period. The mixture compositions of Sigma PCB, Sigma DDT, and Sigma HCH changed during the previous decades indicating decreasing releases of PCB mixtures, DDT, and technical HCH mixtures. The pollutant concentrations currently found in the tern eggs are compared with those of other bird species from other Baltic Sea subregions, suggesting a relatively low pollution of the Belt Sea. The temporal trends in contamination are related to international measurements and conventions on bans of pollutants. Since individually known females were recaptured up to three times, inter-individual variation in pollutant burdens could be studied. Remarkable variation among individuals as well as between breeding seasons were found that were not explainable by general temporal trends. Influences of individually and seasonally varying feeding habits on this phenomenon are discussed. Compositions of individual PCB mixtures varied in relation to total PCB concentrations found in eggs suggesting a concentration-dependent metabolization of PCBs as with other species. Amounts of particular organochlorines varied between matrices possibly indicating metabolization of low chlorinated PCBs, beta-HCH, and HCB during embryogenesis. In mercury, body detoxification via down is assumed. As indicated by eggshell parameters (thickness and index) being not related to organochlorine concentrations and being similar to that found in historical studies, respectively, effects of recent organochlorine contamination on eggshell thickness seem to be improbable. In conclusion, influences of contamination on declining little tern stocks observed in Germany are discussed. Negative influences of contamination in the 1960s and 1970s are assumed to be probable.     

Comparative embryotoxicity of a pentabrominated diphenyl ether mixture to common terns (Sterna hirundo) and American kestrels (Falco sparverius)

Concentrations of polybrominated diphenyl ethers (PBDEs) in Forster’s tern (Sterna forsteri) eggs from San Francisco Bay have been reported to range up to 63 μg g⁻¹ lipid weight. This value exceeds the lowest-observed-adverse-effect level (1.8 μg g⁻¹ egg wet weight; ∼32 μg⁻¹ lipid weight) reported in an embryotoxicity study with American kestrels (Falco sparverius). As a surrogate for Forster’s terns, common tern (Sterna hirundo) eggs were treated by air cell injection with corn oil vehicle (control) or a commercial penta-BDE formulation (DE-71) at nominal concentrations of 0.2, 2, and 20 μg g⁻¹ egg. As a positive control, kestrel eggs received vehicle or 20 μg DE-71 g⁻¹ egg. In terns, there were no effects of DE-71 on embryonic survival, and pipping or hatching success; however, treated eggs hatched later (0.44 d) than controls. Organ weights, organ-to-body weight ratios, and bone lengths did not differ, and histopathological observations were unremarkable. Several measures of hepatic oxidative stress in hatchling terns were not affected by DE-71, although there was some evidence of oxidative DNA damage (8-hydroxy-deoxyguanosine; 8-OH-dG). Although DE-71 did not impair pipping and hatching of kestrels, it did result in a delay in hatch, shorter humerus length, and reduced total thyroid weight. Concentrations of oxidized glutathione, reduced glutathione, thiobarbituric acid reactive substances, and 8-OH-dG in liver were greater in DE-71-treated kestrels compared to controls. Our findings suggest common tern embryos, and perhaps other tern species, are less sensitive to PBDEs than kestrel embryos.     

环境中内分泌干扰物质的研究概述

在总结最新文献的基础上,就环境中的内分泌干扰物质的概念,研究背景,研究方法,在环境中的分布情况作了简单综述和介绍,并对有待开展的研究提出了建议,为国内在环境内分泌干扰物方面的研究提供参考。     

Perfluorinated chemicals in relation to other persistent organic pollutants in human blood

In order to evaluate blood levels of some perfluorinated chemicals (PFCs) and compare them to current levels of classical persistent organic pollutants (POPs) whole blood samples from Sweden were analyzed with respect to 12 PFCs, 37 polychlorinated biphenyls (PCBs), p,p'-dichlorodiphenyl-dichloroethylene (DDE), hexachlorobenzene (HCB), six chlordanes and three polybrominated diphenyl ethers (PBDEs). The median concentration, on whole blood basis, of the sum of PFCs was 20-50 times higher compared to the sum of PCBs and p,p'-DDE, 300-450 times higher than HCB, sum of chlordanes and sum of PBDEs. Estimations of the total body amount of PFCs and lipophilic POPs point at similar body burdens. While levels of for example PCBs and PBDEs are normalized to the lipid content of blood, there is no such general procedure for PFCs in blood. The distributions of a number of perfluorinated compounds between whole blood and plasma were therefore studied. Plasma concentrations were higher than whole blood concentrations for four perfluoroalkylated acids with plasma/whole blood ratios between 1.1 and 1.4, whereas the ratio for perflurooctanesulfonamide (PFOSA) was considerably lower (0.2). This suggests that the comparison of levels of PFCs determined in plasma with levels determined in whole blood should be made with caution. We also conclude that Swedish residents are exposed to a large number of PFCs to the same extent as in USA, Japan, Colombia and the few other countries from which data is available today.     

Ecochemical assessment of environmental chemicals Part I: Standard screening procedure to evaluate chemicals in plant cell cultures

A standard screening procedure using sterile soybean and wheat cell suspension cultures has been developed to study the metabolic profiles of established xenobiotics as well as new synthesized compounds. This short term test provides quantitative data on the distribution of metabolites and the parent compound between the nutrient medium and the plant cells, on the amount of more and less polare metabolite fractions in comparison to the parent compound and the amount of substance bound or irreversibly absorbed to the extracted cell fragments. From this data turnover rates are calculated for ranking purpose. Results obtained for 2,4-D, PCP, DEHP and monolinuron as model substances are presented and compared with data from other environmental tests.     

Water quality guidelines for chemicals: learning lessons to deliver meaningful environmental metrics

Many jurisdictions around the globe have well-developed regulatory frameworks for the derivation and implementation of water quality guidelines (WQGs) or their equivalent (e.g. environmental quality standards, criteria, objectives or limits). However, a great many more still do not have such frameworks and are looking to introduce practical methods to manage chemical exposures in aquatic ecosystems. There is a potential opportunity for learning and sharing of data and information between experts from different jurisdictions in order to deliver efficient and effective methods to manage potential aquatic risks, including the considerable reduction in the need for aquatic toxicity testing and the rapid identification of common challenges. This paper reports the outputs of an international workshop with representatives from 14 countries held in Hong Kong in December 2011. The aim of the workshop and this paper was to identify ‘good practice’ in the development of WQGs to deliver to a range of environmental management goals. However, it is important to broaden this consideration to cover often overlooked facets of implementable WQGs, such as demonstrable field validation (i.e. does the WQG protect what it is supposed to?), fit for purpose of monitoring frameworks (often an on-going cost) and finally how are these monitoring data used to support management decisions in a manner that is transparent and understandable to stakeholders. It is clear that regulators and the regulated community have numerous pressures and constraints on their resources. Therefore, the final section of this paper addresses potential areas of collaboration and harmonisation. Such approaches could deliver a consistent foundation from which to assess potential chemical aquatic risks, including, for example, the adoption of bioavailability-based approaches for metals, whilst reducing administrative and technical burdens in jurisdictions.     

Biodegradation of chemicals in a standardized test and in environmental conditions

The estimation of biodegradation rates is an important source of uncertainty in chemical risk assessment. The existing OECD tests for ready biodegradability have been developed to devise screening methods to determine whether a chemical is potentially easily biodegradable, rather than to predict the actual rate, of biodegradation in the environment. However, risk assessment needs degradation rates. In practice these rates are often estimated (default values) from ready biodegradability tests. These tests have many compromising arbitrary features compared to the situation in the real environment. One important difference is the concentration of the chemical. In wastewater treatment or in the environment many chemicals are present at ng l(-1) to microg l(-1) levels whereas in the tests the concentrations exceed 10-400 mg carbon per litre. These different concentrations of the chemical will lead to different growth kinetics and hence different biodegradation rates. At high concentrations the chemical, if it is degradable, can serve as a primary substrate and competent microorganisms will grow exponentially, resulting in a sigmoid biodegradation curve. At low environmental concentrations the chemical does not serve as a primary substrate, and therefore does not support significant growth of the degraders, and the substrate has a linear biodegradation rate. In this study the biodegradation rates of two reference chemicals, aniline and 4-chloroaniline, were compared in a standard method and in more realistic conditions at low concentrations, using 14C-labelled substances and different sources of inocula. Biomass evolution during the tests was monitored by adenosine triphosphate measurement and also on the basis of the residual 14C-activity in the particulate matter. The results partly support the thesis that low concentrations lead to different biodegradation kinetics compared to the concentrations used in the standard tests. Furthermore the biodegradation rates of the chemicals studied, particularly of 4-chloroaniline, in Finnish natural waters appeared to be lower than those reported in some other countries.     

Bringing together raptor collections in Europe for contaminant research and monitoring in relation to chemicals regulations

Raptors are good sentinels of environmental contamination and there is good capability for raptor biomonitoring in Europe. Raptor biomonitoring can benefit from natural history museums (NHMs), environmental specimen banks (ESBs) and other collections (e.g. specialist raptor specimen collections). Europe’s NHMs, ESBs and other collections hold large numbers of raptor specimens and samples, covering long periods of time. These collections are potentially a valuable resource for contaminant studies over time and space. There are strong needs to monitor contaminants in the environment to support EU and national chemical management. However, data on raptor specimens in NHMs, ESBs and other collections are dispersed, few are digitised, and they are thus not easy to access. Specimen coverage is patchy in terms of species, space and time. Contaminant research with raptors would be facilitated by creating a framework to link relevant collections, digitising all collections, developing a searchable meta-database covering all existing collections, making them more visible and accessible for contaminant research. This would also help identify gaps in coverage and stimulate specimen collection to fill gaps in support of prioritised contaminant monitoring. Collections can further support raptor biomonitoring by making samples available for analysis on request.     

Ecochemical assessment of environmental chemicals Part 2: Standard supplementary screening procedure to evaluate more volatile and less persistent chemicals in plant cell cultures

The described methodology allows the determination of metabolic turnover, biomineralization and volatilization of organic environmental chemicals. The overall accountability of radiolabelled chemicals with standardized soybean and wheat cell cultures determined is nearly quantitative. The total balance of the radiolabelled dichlofluanid, 2,4-dichlorophenoxyacetic acid, monolinuron, lindane, parathion and pentachlorophenol recovered by this method are reported.     

Ecochemical assessment of environmental chemicals: Draft guideline of the test procedure to evaluate metabolism and degradationof chemicals by plant cell cultures

A guideline is drafted describing the screening procedure in detail. The aim for this is to facilitate an adoption of this test by bodies supervising environmental chemicals. Successful introduction of this method into the respective laboratories will cause no problems, as the procedure has been collaboratively established and improved.     

Use of OECD premarket data in environmental exposure analysis for new chemicals

As part of the OECD Chemicals Group program, much effort has gone into trying to identify and develop methodologies for predicting human and environmental exposure to new chemicals. This paper reviews this activity and discusses the applicabilities and limitations of the methodologies. Of special interest is the model developed by Mackay and adapted by Wood that can be used at several levels of sophistication depending on the chemical and environmental data available.     

Seasonal and diurnal gas exchange differences in ozone-sensitive common milkweed (Asclepias syriaca L.) in relation to ozone uptake

Stomatal conductance and net photosynthesis of common milkweed (Asclepias syriaca L.) plants in two different soil moisture regimes were directly quantified and subsequently modeled over an entire growing season. Direct measurements captured the dynamic response of stomatal conductance to changing environmental conditions throughout the day, as well as declining gas exchange and carbon assimilation throughout the growth period beyond an early summer maximum. This phenomenon was observed in plants grown both with and without supplemental soil moisture, the latter of which should theoretically mitigate against harmful physiological effects caused by exposure to ozone. Seasonally declining rates of stomatal conductance were found to be substantial and incorporated into models, making them less susceptible to the overestimations of effective exposure that are an inherent source of error in ozone exposure indices. The species-specific evidence presented here supports the integration of dynamic physiological processes into flux-based modeling approaches for the prediction of ozone injury in vegetation.     

Alcohol ethoxysulfates (AES) in environmental matrices

Environmental Science and Pollution Research - Extensive use of surfactants in numerous fields resulted in their discharge into various environmental compartments including soil, sediment, and...     

Occurrence and treatment trials of endocrine disrupting chemicals (EDCs) in wastewaters

This study demonstrates that both synthetic and natural endocrine disrupting chemicals (EDCs) (e.g., bisphenol A, estrone and 17beta-estradiol) were found in the crude wastewaters from two wastewater treatment works (WwTWs). Conventional biological processes can lower EDCs concentrations to several tens to hundreds ngl(-1). Since natural EDCs (e.g., estrone and 17beta-estradiol) have biological activity and adverse impact on the environment at extremely low concentrations (several tens of ngl(-1)), further treatment after conventional biological processes is required. Preliminary trials with ferrate(VI) and electrochemical oxidation process demonstrated that both processes can effectively reduce EDCs to very low levels, ranging between 10 and 100ngl(-1), but the former is more effective than the latter to reduce COD concentration in wastewater for given studying conditions.     

Monitoring, modelling and environmental exposure assessment of industrial chemicals in the aquatic environment

Monitoring and laboratory data play integral roles alongside fate and exposure models in comprehensive risk assessments. The principle in the European Union Technical Guidance Documents for risk assessment is that measured data may take precedence over model results but only after they are judged to be of adequate reliability and to be representative of the particular environmental compartments to which they are applied. In practice, laboratory and field data are used to provide parameters for the models, while monitoring data are used to validate the models' predictions. Thus, comprehensive risk assessments require the integration of laboratory and monitoring data with the model predictions. However, this interplay is often overlooked. Discrepancies between the results of models and monitoring should be investigated in terms of the representativeness of both. Certainly, in the context of the EU risk assessment of existing chemicals, the specific requirements for monitoring data have not been adequately addressed. The resources required for environmental monitoring, both in terms of manpower and equipment, can be very significant. The design of monitoring programmes to optimise the use of resources and the use of models as a cost-effective alternative are increasing in importance. Generic considerations and criteria for the design of new monitoring programmes to generate representative quality data for the aquatic compartment are outlined and the criteria for the use of existing data are discussed. In particular, there is a need to improve the accessibility to data sets, to standardise the data sets, to promote communication and harmonisation of programmes and to incorporate the flexibility to change monitoring protocols to amend the chemicals under investigation in line with changing needs and priorities.     

中国环境内分泌干扰物的污染现状分析

内分泌干扰物严重威胁着全球环境和生态健康,基于人为源内分泌干扰物的分类,分析了国内内分泌干扰物的污染现状,指出了目前研究工作的局限,提出了今后研究重点及污染控制的建议。     

Steps towards environmental hazard assessment of new chemicals (including a hazard ranking scheme,based upon directive 79/831/EEC)

Directive 79/831/EEC came into force on 18th September 1981, enabling all the Member States of the EEC to classify so-called “new chemicals” with respect to their potential hazard to the environment and to human health on a standardized basis (Directive 79/831/EEC, Annex VII). The authors are of the opinion that the assessment of the “environmental hazard” of new chemicals before they are placed on the market, represents, in the present critical economic /ecological situation, which practically all the Member States have in common, a particular challenge to the scientific community and the competent authorities. The comments aim to achieve the following - to provide a more precise definition of certain key terms and to point out a way of selecting from the bundle of new chemicals those (few) which are potentially hazardous; a way which is clear to the administration, the scientific community, industry and, not least of all, to the individual as taxpayer and consumer.