Environmental hazard screening of a metal-polluted site using pressurized liquid extraction and two in vitro bioassays

Rapid screening methods can improve the cost effectiveness, throughput, and quality of risk assessments of contaminated sites. In the present case study, the objective was to evaluate a combination of pressurized liquid extraction and 2 in vitro bioassays for the hazard assessment of surface soil sampled from 46 points across a pyrotechnical industrial site. Pressurized liquid extraction was used to rapidly produce soil-water extracts compatible with 2 high-capacity bioassays. Hazard assessment using combined toxicological and chemical screening revealed zones with relatively high potential risks of metal pollution. Multivariate data analysis provided indications that significant inhibition in the bioassays was correlated with levels of metals in the extracts, suggesting an elevated toxic potential from certain metals. Low pH and high concentrations of dissolved organic carbon were associated with increased cytotoxicity of extracts, indicating that these factors influence metal bioavailability. The cytotoxicity observed was more strongly correlated to metal concentrations in the extracts than in the soil, suggesting that measurements of total metal concentrations in soils do not provide good indications of the soil's potential toxicity.     

Partitioning of chloroaromatic compounds between the aqueous phase and dissolved and particulate soil organic matter at chlorophenol contaminated sites

The retention and mobility of hydrophobic organic contaminants (HOCs) in soil is mainly determined by hydrophobic partitioning to dissolved and particulate organic matter (DOM and POM, respectively). The aqueous phase, DOM, and POM fractions were extracted and separated from soils at three sites contaminated with technical chlorophenol formulations. Concentrations of chlorophenols (CP), polychlorinated phenoxyphenols (PCPP), polychlorinated diphenyl ethers (PCDE) and polychlorinated dibenzo-p-dioxins and furans (PCDD/F) were determined. The partitioning to POM, in relation to DOM, increased in all three soils with increasing hydrophobicity in the order CP < PCPP ~ PCDE ~ PCDF < PCDD. Differences in partitioning to DOM (logK(DOC)) and POM (logK(POC)) could not be explained by differences in gross organic C chemistry. Black carbon did not contribute significantly to the sorption of PCDDs, whereas >70% wood fibre in one soil resulted in a decrease of logK(POC) of 0.5 units for CPs and PCDDs. We conclude that logK(OC) for both DOM and POM need to be explicitly determined when the retention and mobility of HOCs is described and modelled in soils.     

Male contests in the scarlet rosefinch (Carpodacus erythrinus) in relation to asymmetries in resource holding power and pairing status

Summary Inter-male contests in relation to asymmetries in their pairing status and resource holding power were studied in a population of the Scarlet rosefinch. Since males in this species do not defend territories before nest building, and since most males have full adult plumage, possession of territory and age are unlikely to be used as cues in the settlement of contests. Rather, two other features are used, namely size and pairing status. In this study, contests between two unpaired males were usually short displacements, whereas 56% of contests between two paired males were escalated. In the first case, the smaller male withdrew in all contests, whereas in the second case there was an equal probability of withdrawal with regard to size. There was no relationship between size difference and the probability of escalation in the contests. Most of the fights between paired and unpaired males escalated, namely in 60% of the cases where the unpaired male was smaller and in 75% of the cases where he was larger. The unpaired male withdrew in 18 out of 23 contests, suggesting that pairing status is more important than size in determining the outcome of a contest. There was no variance in size differences between contestants in short and escalated contests. This study demonstrates that there is a high competition between males for females in this population.     

运用卫星数据和来自国家森林清查的野外数据进行全国森林变量估计

瑞典约有55%的土地面积被森林所覆盖.目前,瑞典的森林覆盖没有统一的和地理学上明晰的描述.现存的独立性数据源是Landsat TM和SPOT HRV卫星数据、地图蒙片(map mask)和森林清查样地.它们在一起,使森林变量(如材枳和林分年龄)的计算机估计成为可能.这些估计的精确度在像素水平上是低的,但在林分水平上较高.在规划木材资源应如何加以利用或出于监测目的时,这类基于栅格的森林数据对政府来说是有帮助的.本文描述了以有效成本建立森林变量估计全国数据库的生成流程.我们在林分水平上评价了瑞典西南部某地森林变量估计的精确度.结果表明,总材积估计的整体均方根误差为33%,年龄估计的整体均方根误差为23%.     

瑞典森林中不同地区的林下植被情况与氮沉积的关系

在557块针叶林分中进行调查,以图了解欧洲越桔(Vacciniummyrtillus)、越桔(V.vitis-idaea)和曲芒发草(Deschampsiaflexuosa)与氮沉积率的相互联系.欧洲越桔在高氮地区比在低氮地区发生频度、丰富度都较少并且易感染叶部病原(Valdensiaheterodoxa),越桔的发生与氮沉积的增加呈明显的负相关,曲芒发草却没有这种趋势.在高氮沉积地区,欧洲越桔在优势种为欧洲赤松的林分中比在挪威云杉为优势种的林分中更为最普遍.在氮沉积较低水平的地区不是这种情形.调查的情况与增施氮素实验的结果一致,氮沉积对植被显示了巨大的效应.数据表明即使是较低的氮沉积也可能减少针叶林分林下植被最优势种的丰富度.     

Does Tephrosia candida as fallow species, hedgerow or mulch improve nutrient cycling and prevent nutrient losses by erosion on slopes in northern Viet Nam?

Agroforestry is considered to be a promising alternative to short-fallow shifting cultivation or other monocropping systems. An on-farm experiment was established in 1996 in northern Viet Nam to examine the contribution of the leguminous bush Tephrosia candida (Roxb.) D.C. as a fallow or hedgerow species and as a mulch producer to improve nutrient cycling and prevent nutrient losses by erosion. The systems tested were upland rice monocropping (Mono), natural fallow (NaFa), fallow of Tephrosia (TepFa), hedgerow intercropping with upland rice (Oryza sativa L.) and internal mulching using pruned Tephrosia biomass (TepAl), and upland rice with external mulching using Tephrosia biomass (TepMu). Over two cropping seasons, from April 1996 to April 1998, nutrients recycled and inputs and exports were recorded, as well as changes in C-, N- and P-pools, and in pH in the 0–5 cm topsoil layer.The Tephrosia systems (TepFa, TepAl, TepMu) prevented nutrient losses by erosion effectively. Compared to the NaFa system, the TepFa system accumulated 34% more N in the above-ground plant parts and increased topsoil N by 20%, probably due to N-fixation. There was a trend that the less labile P-pools (NaOH-P) were reallocated into the more labile P-pools (Bicarb-P) in the soil of the TepFa system. Burning released significant amounts of the inorganic P-pools in both the NaFa and TepFa systems and this effect seemed to be more pronounced in the TepFa than in the NaFa. Organic input to crop export ratios for N and P were >1 in the TepAl and TepMu treatments. This was due to a sufficient quantity and quality of the Tephrosia mulching material. However, moderately labile NaOH-extractable organic P seemed to be depleted in the topsoil due to high P uptake in the TepMu treatment. Thus, nutrient cycling and nutrient balances were improved under the Tephrosia systems. But for long-term P sustainability, there is a belief that a combined use of mulching and mineral P fertiliser is needed.     

Assessing the environmental fate of chemicals of emerging concern: a case study of the polybrominated diphenyl ethers

It is suggested that assessments of chemicals of emerging concern can be rationally structured around a multistage process in which fate and risk are evaluated with increasing accuracy as new data become available. An initial tentative and approximate assessment of fate and risk can identify key data gaps and justify and direct further investigations, which progressively improve the reliability of the assessment. This approach is demonstrated for a class of chemicals, the polybrominated diphenyl ethers (PBDEs), which is of increasing concern, but about which there is presently a lack of comprehensive data on properties, sources, fate and effects. Specifically, 20 PBDE congeners are investigated using the suggested approach and research needs are identified.     

Natural formation and degradation of chloroacetic acids and volatile organochlorines in forest soil--challenges to understanding

- DOI: http:/dx.doi.org/10.1065/espr2005.06.262 Goal, Scope and Background The anthropogenic environmental emissions of chloroacetic acids and volatile organochlorines have been under scrutiny in recent years because the two compound groups are suspected to contribute to forest dieback and stratospheric ozone destruction, respectively. The two organochlorine groups are linked because the atmospheric photochemical oxidation of some volatile organochlorine compounds is one source of phytotoxic chloroacetic acids in the environment. Moreover, both groups are produced in higher amounts by natural chlorination of organic matter, e.g. by soil microorganisms, marine macroalgae and salt lake bacteria, and show similar metabolism pathways. Elucidating the origin and fate of these organohalogens is necessary to implement actions to counteract environmental problems caused by these compounds. Main Features While the anthropogenic sources of chloroacetic acids and volatile organochlorines are relatively well-known and within human control, knowledge of relevant natural processes is scarce and fragmented. This article reviews current knowledge on natural formation and degradation processes of chloroacetic acids and volatile organochlorines in forest soils, with particular emphasis on processes in the rhizosphere, and discusses future studies necessary to understand the role of forest soils in the formation and degradation of these compounds. Results and Discussion Reviewing the present knowledge of the natural formation and degradation processes of chloroacetic acids and volatile organochlorines in forest soil has revealed gaps in knowledge regarding the actual mechanisms behind these processes. In particular, there remains insufficient quantification of reliable budgets and rates of formation and degradation of chloroacetic acids and volatile organochlorines in forest soil (both biotic and abiotic processes) to evaluate the strength of forest ecosystems regarding the emission and uptake of chloroacetic acids and volatile organochlorines, both on a regional scale and on a global scale. Conclusion It is concluded that the overall role of forest soil as a source and/or sink for chloroacetic acids and volatile organochlorines is still unclear; the available laboratory and field data reveal only bits of the puzzle. Detailed knowledge of the natural degradation and formation processes in forest soil is important to evaluate the strength of forest ecosystems for the emission and uptake of chloroacetic acids and volatile organochlorines, both on a regional scale and on a global scale. Recommendation and Perspective As the natural formation and degradation processes of chloroacetic acids and volatile organochlorines in forest soil can be influenced by human activities, evaluation of the extent of this influence will help to identify what future actions are needed to reduce human influences and thus prevent further damage to the environment and to human health caused by these compounds.     

A study on the potential sources of air pollutants observed at Tjörn,Sweden

The Potential Source Contribution Function (PSCF) receptor model combines both chemical and meteorological information. In this study, PSCF was employed to identify the potential source emission regions for aerosol compositions measured at Tjörn, Sweden (58.01 °N, 11.36 °E). PSCF was for the first time applied on a European scale. One hundred and fifty-two four-day air parcel backward trajectories were combined with concentrations of sixteen elements determined in 33 coarse and fine aerosol samples. The observations were made between February 17 and March 26, 1985. The modeling results of the heavy metals V, Pb, Zn, and As are presented and compared with available emission inventory data. A number of known industrialized regions in the former USSR and Europe are found of high potential to be the emission source areas. These areas are in good agreement with the known emission information. The PSCF maps of total sulfur, Non-Seasalt-Sulfur (N.S.S.) and chlorine are also presented. High potential regions in the Arctic area exist in the PSCF map for total sulfur wheres they do not occur in that for N.S.S.     

Chlorinated terpenes and chlordane components found in fish,guillemot and seal from Swedish waters

Fish samples from the Baltic, the North Sea and lake Vättern have been found to be contaminated with chlorinated terpenes. These compounds were also present in seal and guillemot from the Baltic at the same concentration - about 10 mg per kg fat - as in their prey, the herring. Chlordane-related compounds were also found in all samples. The most common substances were trans-nonachlor and oxychlordane, but differences could be observed between species. These organochlorine pesticides are not used in Sweden and the probable explanation for their presence in a Swedish lake is air transportation.