Combination of two indication systems in pre-alpine lakes — diatom index and macrophyte index

Since the climax of eutrophication in the early 1980s mainly greater lakes have been investigated and monitored in terms of their nutrient charge. In the future there will still be a need to develop guidelines for monitoring the trophic status of smaller lakes. Four small lakes were investigated by the author in the years 1996 and 1997. In order to define the nutrient charge of those lakes more precisely, special emphasis has been put upon the two criteria diatoms and macrophytes. Eventually an evaluation of the lakes' catchment areas will also be an important component of these studies. Benthic diatoms are the main part of periphyton. As unicellular fast reproducing organisms they are excellent indicators for trophic situations in lakes. The diatom index denotes the trophic status of the littoral zone during the last few weeks before sampling. The macrophytes, however, reflect the nutrient charge over a longer period, i.e. several years. The macrophyte index is based on the fact that some species are most prevalent at certain nutrient loads. The effort to combine these two indication systems carries a high resolution of spatial nutrient changes as well as in temporally changes.     

使用安捷伦7000A三重串联四极杆GC/MS/MS系统测定大气颗粒物中的硝基多环芳烃

采用毛细管GC结合安捷伦7000A三重串联四极杆GC/MS(G7010AA)系统的多反应监测(MRM)模式分析了大气颗粒物中的硝基多环芳烃(nitro-PAHs).传统硝基多环芳烃的分析方法是在样品前处理之后,使用单四极杆GC/MS的选择离子监测SIM模式或者多维GC/MS,但基于MS/MS检测模式超强的选择性,可直接分析大气颗粒物的粗提物.实际样品中的硝基多环芳烃可以检测到pg·μL-1的级别,相对应于大气样品中pg·m-3级的含量.     

纳米二氧化钛在老化环境条件下对铜诱导毒性的影响

纳米二氧化钛颗粒(nTiO₂)可以通过吸附表层水中共生重金属来改变它们对淡水无脊椎动物的毒性。然而,影响这种交互过程的几种环境因子的相对重要性仍不清楚。因此,本研究通过连续72 h的培养试验,评估了老化对Cu与nTiO₂对大型蚤Daphnia magna联合急性毒性的影响。在老化过程中,对老化时间以及离子强度、pH值和不同质量有机物质等因子都进行了考察。研究结果表明,尽管影响效应的大小不同,nTiO₂的存在往往减少了老化后Cu对大型蚤的诱发毒性,在没有nTiO₂的情况下,Cu对大型蚤急性毒性的EC₅₀值提高了3倍之多。此外,各种形态Cu的形成受到介质中的离子组成、pH值以及有机添加剂存在的影响,这一过程受到极大的调控,并随着老化时间对大型蚤生态毒性的响应有一定影响。尽管如此,该研究的结论对nTiO₂在淡水生态系统中不同环境条件下,改变重金属诱发毒性的潜在作用提供了有力的支持。然而,这种模式需要进一步验证,比如结合不同性质的重金属离子与不同的环境因素,如紫外线照射。
精选自Ricki R. Rosenfeldt, Frank Seitz, Ann-Cathrin Haigis, Johanna H?ger, Jochen P. Zubrod, Ralf Schulz, Mirco Bundschuh. Nanosized titanium dioxide influences copper induced toxicity during aging as a function of environmental conditions. Environmental Toxicology and Chemistry: Volume 35, Issue 7, pages 1766–1774, July 2016. DOI: 10.1002/etc.3325
详情请见http://onlinelibrary.wiley.com/doi/10.1002/etc.3325/full
     

An economic evaluation framework for land-use-based conservation policy instruments in a changing climate

Climate change is a key threat to biodiversity. To conserve species under climate change, ecologists and conservation scientists suggest 2 main conservation strategies regarding land use: supporting species’ range shifts to enable it to follow its climatic requirements by creating migration pathways, such as corridors and stepping stones, and conserving climate refugia (i.e., existing habitat areas that are somewhat buffered from climate change). The policy instruments that could be used to implement these conservation strategies have yet to be evaluated comprehensively from an economic perspective. The economic analyses of environmental policy instruments are often based on ecological effectiveness and cost-effectiveness criteria. We adapted these general criteria to evaluate policy instruments for species’ conservation under climate change and applied them to a conceptual analysis of land purchases, offsets, and conservation payments. Depending on whether the strategy supporting species’ range shifts or conserving climate refugia is selected, the evaluation of the policy instruments differed substantially. For example, to ensure ecological effectiveness, habitat persistence over time was especially important for climate refugia and was best achieved by a land-purchase policy instrument. In contrast, for the strategy supporting range shifts to be ecologically effective, a high degree of flexibility in the location of conserved sites was required to ensure that new habitat sites can be created in the species’ new range. Offset programs were best suited for that because the location of conservation sites can be chosen comparatively freely and may also be adapted over time.     

Inhibition of tetrachloromethane-induced cross-linking of microsomal fatty acids by the spin-trap α-phenyl- N - t -butylnitrone

The effect of the spin-trap α-phenyl-N-t-butylnitrone (PBN) on the formation of fatty acid dimers induced by the anoxic microsomal metabolism of tetrachloromethane was investigated in vitro, in particular, with respect to cross-linking of arachidonic acid with a second one (C₂₀–C₂₀) and of arachidonic acid with docosahexaenoic acid (C₂₀–C₂₂). PBN exerted no effect on anaerobic tetrachloromethane metabolism but inhibited dimer formation, half-maximally at a concentration of 0.1 mmol L^?1. Trichloromethyl octadecenoic acid was also found, but at levels 10-fold lower than the fatty acid dimers. The data suggest that the hepato-protective effect of PBN against tetrachloromethane-toxicity may be due to its ability to scavenge fatty acid radicals, resulting in stable, non-reactive entities, which do not undergo secondary reactions such as cross-linking. The data confirm and extend previous findings that crosslinking plays an important role in tetrachloromethane toxicity and similar cases of metabolic radical-induced toxicity.     

Assessment of heavy metals in a soil contaminated by oil spill: a case study in Nigeria

Surface and subsurface soil samples contaminated with crude oils were collected from an impacted site at Bodo City in the Niger Delta, Nigeria, after a field reconnaissance survey. An uncontaminated soil sample collected 100 m from the impacted site, but within the same geographical area, was used as a control. Trace elements such as, As, Cu, Cr, Cd, Fe, Pb, Ba, Ni, V, Hg and cation-exchange capacity constituents of the contaminated and uncontaminated soils were determined by atomic absorption spectroscopy. Trace element concentrations were: Cu, 0.5–13.4 mg kg^{? 1}; Cr, 0.2–0.8 mg kg^{? 1}; Fe, 6.2–8.7 mg kg^{? 1}; Ba 80.0–108.0 mg kg^{? 1}; Ni, 0.6–4.8 mg kg^{? 1}; and V, 4.0–9.4 mg kg^{? 1}; cation-exchange capacity ranged from 43.6 to 57.2 mg kg^{? 1} in surface and subsurface soils. Results showed that eigenvalues for the two first principal components represent up to 49% of the total variance. A positive correlation of the first principal component with Cu, Cr and cation-exchange capacity shows pollution from oil spillage, while a positive correlation of the second principal component with Cr, Fe, V, and dissolved oxygen (DO) shows both oil pollution and allochthonous inputs.     

Environmental fate of pesticides used in Australian viticulture III. Fate of dithianon from vine to wine

Pinot noir, bastardo, rkaziteli and semillon grapes on vines grown in the Barossa Valley of South Australia were treated with a commercial dithianon formulation. The grapes were harvested by hand eight days later, and made into wine. Grab samples of berries, grape juice and the young wine were analysed for fungicide residues. No dithianon was detected in control grape samples, grape juices or wines. Significant dithianon levels were detected on the skins of treated grape samples. Dithianon is stable on the surface of grapes under the ambient conditions prevalent under the grape canopy for at least two weeks. No dithianon was detected in grape juice, on grape skins after berry crushing, in the lees, or in the young wine. Dithianon is unstable in grape juice and wine. Dithianon half‐life (initial concentration = 1 μg/mL) in semillon grape juice = 2.8 h, semillon wine = 0.58 h, pinot noir grape juice = 4.6 h, and pinot‐noir wine = 0.29 h. Treatment with fining agents or heat does not significantly reduce the rate of degradation. These results suggest that spraying table grapes with dithianon two weeks before harvest would result in exposure to essentially the full dose of active ingredient sprayed, and increase the risk to human health through ingestion of this compound. However, any threat to human health from ingestion through grape juice or wine is limited since any contact with grape juice or wine leads to rapid decomposition of dithianon by some as yet undetermined process.