焦化废水中有机污染物好氧生物降解特性的研究

在实验室条件下,采用瓦勃氏微量呼吸仪测试方法,以处理焦化废水曝气池内活性污泥作为降解所用微生物,研究了焦化废水中咪唑等6种有机污染物的好氧生物降解特性。文中的对这些有机污染物在单一基质和与苯酚共基质条件下的降解规律、它们对微生物的抑制情况进行了详细考察。在与苯酚共基质条件下,6种有机污染物的降解特性有不同程度变化。吩噻嗪、高浓度萘和咔唑抑制苯酚降解,咪唑、吡咯、蒽在共基质条件下降解性有所提高     

淡水水体底泥中厌氧氨氧化菌的原位鉴别

采用16S rRNA方法对江苏省新沂河的底泥样品进行了厌氧氨氧化菌的原位检测,建立了样品的16S rRNA克隆文库,共包括6个16S rRNA克隆序列.对文库中克隆序列利用ARB软件包进行了排队分析及系统发育树的绘制.分析结果表明,新沂河底泥样品中含有与已知厌氧氨氧化菌Candidatus“Brocadia anammoxidans”相似性为91%的16S rRNA基因,经鉴定为厌氧氨氧化菌Brocadia分支的新种类.样品中还含有组成Planctomycetes新分支的16S rRNA基因,它们与已知厌氧氨氧化菌序列的遗传距离较远,其微生物特性还有待进一步研究.厌氧氨氧化菌在淡水环境中的发现将有助于进一步研究厌氧氨氧化过程在受损淡水生态系统修复重建中的作用,重新认识其中的氮循环过程.     

Molecular phylogenies help resolve taxonomic confusion with Asian <Emphasis Type="Italic">Crassostrea</Emphasis> oyster species

Identification of oyster species is still largely based on phenotypic characters that are highly plastic. Prompted by the proposed introduction of the Asian oyster species Crassostrea ariakensis into the Chesapeake Bay region of the U.S.A., this study uses molecular genetic information to understand the taxonomic framework surrounding C. ariakensis and to confidently distinguish among various sympatric oyster species. Putative samples of C. ariakensis and other species of cupped oysters from across Asia were collected and phylogenetic analyses were conducted on DNA sequences of both nuclear (ITS-1) and mitochondrial (COI) regions. Trees generated based on the two independent molecular datasets were highly congruent, and indicate that many oysters collected for this study as C. ariakensis were originally misidentified. Results also indicate that C. ariakensis, C. hongkongensis and C. nippona are distinct, but closely related species. There is strong support in both analyses for a close relationship between C. gigas and C. sikamea, as well as between C. belcheri and C. gryphoides, and between C. iredalei and C. madrasensis. The parsimony analyses based on these DNA markers, however, did not provide evidence to support C. angulata as a distinct species from C. gigas. Overall, the results emphasize the need for rigorous species identification, and additional extensive and intensive sampling to more accurately determine relationships among Crassostrea species, define their geographic distributions, and establish existing sympatry patterns.     

Book review

Environmental Management, (3 Volumes) Editors B. Nath, L. Hens and D. Devuyst (Brussels, Vubpress: 1993. Approx. 890 Pp. Paperback) (£25 Per Volume) Isbn 90 5487 035 4-6

The Chemistry and Deposition of Nitrogen Species in the Troposphere, Editor A. T. Cocks, Publisher Royal Society of Chemistry, 1993, X + 134pp., Isbn 0 85186 355 8, Price £35.00.     

Polyfluoroalkyl compounds in landfill leachates

Polyfluoroalkyl compounds (PFCs) are widely used in industry and consumer products. These products could end up finally in landfills where their leachates are a potential source for PFCs into the aqueous environment. In this study, samples of untreated and treated leachate from 22 landfill sites in Germany were analysed for 43 PFCs. ΣPFC concentrations ranged from 31 to 12,819 ng/L in untreated leachate and 4-8060 ng/L in treated leachate. The dominating compounds in untreated leachate were perfluorobutanoic acid (PFBA) (mean contribution 27%) and perfluorobutane sulfonate (PFBS) (24%). The discharge of PFCs into the aqueous environment depended on the cleaning treatment systems. Membrane treatments (reverse osmosis and nanofiltrations) and activated carbon released lower concentrations of PFCs into the environment than cleaning systems using wet air oxidation or only biological treatment. The mass flows of ∑PFCs into the aqueous environment ranged between 0.08 and 956 mg/day.     

Metal availability in a highly contaminated, dredged-sediment disposal site: Field measurements and geochemical modeling

Two complementary approaches were used to characterize arsenic and metal mobilizations from a dredged-sediment disposal site: a detailed field study combined with hydrogeochemical modeling. Contaminants in sediments were found to be mainly present as sulfides subject to oxidation. Secondary phases (carbonates, sulfates, (hydr)oxides) were also observed. Oxidative processes occurred at different rates depending on physicochemical conditions and contaminant contents in the sediment. Two distinct areas were identified on the site, each corresponding to a specific contaminant mobility behavior. In a reducing area, Fe and As were highly soluble and illustrated anoxic behavior. In well-oxygenated material, groundwater was highly contaminated in Zn, Cd and Pb. A third zone in which sediments and groundwater were less contaminated was also characterized. This study enabled us to prioritize remediation work, which should aim to limit infiltration and long-term environmental impact.     

Factors affecting the growth rates of ammonium and nitrite oxidizing bacteria

The maximum specific growth rates of both ammonium oxidizing bacteria (AOB) and nitrite oxidizing bacteria (NOB) were investigated under varying aerobic solids retention time (SRT_a) and in the presence/absence of anoxic (alternating) conditions. Two bench SBRs, reactor R1 and R2, were run in parallel for 150 d. Reactor R1 was operated in aerobic conditions while R2 operated in alternating anoxic/aerobic conditions. The feed (synthetic wastewater), temperature, hydraulic retention time and mixing were identical in both reactors. The SRT_a in both reactors was, sequentially, set at four values: 5, 4, 3 and 2 d.Kinetic tests with the biomasses from both reactors were carried out to estimate the maximum specific growth rates (μ_max) at each tested SRT_a and decay rates, in both aerobic and anoxic conditions. The kinetic parameters of nitrifier were estimated through the calibration of a two step nitrification-denitrification activated sludge model.The results point to a slightly higher μ_max,AOB and μ_max,NOB in alternating conditions, while both μ_max,AOB and μ_max,NOB were shown not to vary in the tested range of SRT_a (from 2 to 5 d) at 20 °C. They were relatively high when compared to literature data: 1.05 d⁻¹ < μ_max,AOB < 1.4 d⁻¹ and 0.91 d⁻¹ < μ_max,NOB < 1.31 d⁻¹. The decay coefficients of both AOB and NOB were much higher in aerobic (from 0.22 d⁻¹ to 0.28 d⁻¹) than in anoxic (0.04 d⁻¹ to 0.16 d⁻¹) conditions both in R1 and R2, which explained the higher nitrification rates observed in the alternating reactor.     

Status and prospects of pay-as-you-throw in Europe - a review of pilot research and implementation studies

Over the past 20 years, significant advances have been made in developing efficient schemes to charge households for their actual waste generation. Viable fee models and technical solutions which are applicable to different environments and provide waste generators with individual incentives for waste diversion efforts have increased the recognition of pay-as-you-throw (PAYT) as an effective instrument for recycling-oriented waste management and financing. On this basis, PAYT has become a practical reality in an increasing number of countries in Europe. Even countries with traditional reservations for direct charging have started to make consideration of PAYT in the revision of their national policy programmes. A situational analysis performed at the European level showed that detailed insights regarding the concrete reactions, red flags and wider benefits inherent to such scheme may still have to be further dispersed in order to overcome the caveats on PAYT and eventually adopt the approach on a larger scale. Claims that the results of PAYT applications are only local in meaning can be disproved as many of the developments bear universal character and can be verified even for larger territories using such schemes in different ways. Including results from an international research co-operation and comparative studies conducted in Germany, this article examines the state-of-the-art of PAYT and shades light onto some of the generally observed implications of its implementation. In conclusion, an outlook on the further potentials and propagation of this scheme is given.     

The environmental state at sea

Seas and oceans are confronted with a plethora of environmental problems, caused by land-based activities (agriculture, industries, and ports) and by maritime activities (such as shipping, fishing, oil and gas drilling, tourism, and navigational dredging). Environmental problems at sea challenge the efficacy of state sovereignty. Who is responsible, accountable, and regulates environmental and spatial problems at the level of regional seas, and what is the role of states in these processes of governance? In the regional seas and on the high seas, the environmental state is challenged by two developments: states become players at different levels, and states are confronted with the activities of big market players where they have no or little jurisdiction. The different forms of the environmental state in Europe’s regional seas and in the Arctic Ocean are examined.     

Qualitative structure residue relationship analysis in the determination of the maximum residue limit of veterinary drugs

Aim of the present study was an attempt to find a correlation between physicochemical structure of veterinary drugs and the maximum residue limit (MRL) for muscle tissue of food producing animals. Direct correlation and analysis in quintile groups for 52 physicochemical parameters were performed. An internal validation using leave-one-out cross-validation was performed. In the quintile groups, there were 11 arithmetic expressions created for the limited group of individual parameters (13 from 52 analyzed), which showed a significant linear or quadratic correlation between the number of quintile group and the mean value of MRL within the quintile. The results obtained suggest that there is no direct correlation between individual physicochemical parameters and MRL value in muscle tissue; however, such correlation can be determined for arithmetic expressions created on the basis of several physicochemical parameters, using quintile group analysis.