脱卤球菌纲(Dehalococcodia Class)在有机卤化物生物地球化学循环中的作用

脱卤球菌(Dehalococcoidia,Dia)纲是绿弯菌门下属八大纲之一.迄今为止,脱卤球菌纲中包含3个能进行严格厌氧有机卤化物呼吸的菌属:脱卤拟球菌(Dehalococcoides,Dhc)、脱卤单胞菌(Dehalogenimonas,Dhgm)及尚未正式命名的Candidatus"Dehalobium".当前关于脱卤拟球菌和脱卤单胞菌生理学、生物化学和生态学方面的研究,主要集中在从有机氯污染场地中富集或者分离出来的菌株方面.而越来越多的研究证据表明,能进行有机卤化物呼吸的脱卤球菌纲微生物不仅仅只存在于污染物产地,在各种环境(如海洋、淡水、陆地)中也能经常被检测和鉴定到.但脱卤球菌纲微生物在自然界生态系统中起到的重要作用尚未被完全揭示.本文旨在介绍和讨论被低估且未被充分研究的脱卤球菌纲微生物的生理生态特征及其潜在的生态学功能,从而引起研究人员更广泛的关注,鼓励跨学科研究来揭示这一类特殊微生物在有机卤化物生物地球化学循环中的重要作用.     

秦皇岛城市污水处理厂剩余污泥基本性质及农用价值分析

剩余污泥的处理与处置是个世界性的难题。目前的处置方法中，土地利用逐渐被各国所广泛采用。通过对秦皇岛第三、第四污水处理厂的剩余污泥的基本性质进行测试，以此为基础对污泥的农用价值及其应用前景进行分析和展望。     

Effects of four chlorobenzenes on serum sex steroids and hepatic microsome enzyme activities in crucian carp, Carassius auratus

Four chlorobenzenes (chlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene, p-chloro-methylbenzene) were administrated to the crucian carps (Carassius auratus) by peritoneal injections in the laboratory for 30 days. Serum testosterone and 17 beta-estradiol concentrations were detected using radioimmunology assay (RIA), and the activities of two hepatic microsome enzymes, glutathione s-transferase (GST) and UDP-glucuronosyltransferase (UDPGT), were measured using the modified methods as described by Habig and Owens. Results showed that the four chlorobenzenes caused significant increases in serum testosterone concentration in the crucian carps (P < 0.05) compared to the controls, but they caused no significant effect on 17 beta-estradiol level. All test chemicals caused a change in hepatic GST activity in crucian carps, with significant increases in enzyme activity (P < 0.05). Chlorobenzene, 1,3-dichlorobenzene and p-chloro-methylbenzene resulted in a marked inhibition to UDPGT activity in crucian carp (P < 0.05) except 1,4-dichlorobenzene. The changes in hepatic microsome enzyme activities may have resulted in the alterations of serum sex steroids levels in the crucian carps. The results indicated that these four chlorobenzenes may result in the changes of endocrine functions and may affect the reproductive success of this and other species.     

Effect of organic acids on adsorption and desorption of rare earth elements

Effect of citric, malic, tartaric and acetic acids on adsorption of La, Ce, Pr and Nd by and desorption from four typical Chinese soils was studied. Generally, adsorption capacities of rare earth elements (REEs) were significantly correlated with the cation exchange capacity (CEC) of soils. In the presence of acetic acids adsorption of REEs was similar to that in the presence of Ca(NO3)2. However, in the presence of citric, malic and tartaric acids adsorption of REEs by Heilongjiang, Zhejiang and Guangdong soils decreased to varying extents if compared with that in the presence of nitrate and acetic acid. The significance of suppression followed the order of citric acid > malic acid > tartaric acid > acetic acid, which was consistent with the order of stability of complexes of REEs with these organic acids. However, the adsorption increased with increasing equilibrium solution pH. For Jiangxi soil with low soil pH, CEC and organic matter these organic acids exerted an even more serious suppression effect on the adsorption of REEs. Another feature of the relationship between the adsorption of REEs and equilibrium solution pH was that the adsorption of REEs decreased with increase of pH from 2 to 4.5 and then slightly increased with further increase of pH. Desorption of REEs varied with soils and with organic acids as well. REEs were released easily from Heilongjiang, Zhejiang and Guangdong soils in the presence of organic acid. Generally, desorption of REEs decreased with increasing equilibrium solution pH. Effect of organic acids on desorption of REEs from Jiangxi soil was more complicated. In the presence of citric and malic acids no decrement and/or slight increase in desorption of REEs were observed over the equilibrium solution pH from 3 to 6.5. The reasons for this were ascribed to the strong complexing capacity of citric and malic acids and low soil pH, CEC and organic matter of Jiangxi soil.     

Bioaccumulation of mercury in a vestimentiferan worm living in Kagoshima Bay,Japan

The present study reports on the mercury concentrations of the vestimentiferan worm, Lamellibrachia satsuma, (Annelida: Pogonophora) found near hydrothermal vents at a depth of 80-100 m in the northern parts of Kagoshima Bay. The vestimentiferan worms had total mercury concentrations of 238 ng/g in the anterior muscle of the body and 164 ng/g in the posterior trophosome. Methylmercury constituted only 7.6% of total mercury detected anteriorly and 16.3% posteriorly. The mean total mercury concentration in filtrated ambient seawater of the worm habitat was 1.1 ng/l. The worm should accumulate mercury in seawater by a one-step into the anterior and posterior parts as 2.2 x 10(%) and 1.5 x 10(5) times those of the filtered ambient seawater, respectively. The bioaccumulation factor of mercury by the worms with only their respiration would be actually larger than that by other marine animals through food webs. The high bioaccumulation factor of mercury in the worms suggest the following two possibilities: (i) the biological half-life of organomercury in the worm could be exceptionally long; or (ii) the lifetime of vestimentiferan worms examined in the present study could be extremely long. Various metals in one specimen of the worm were analyzed by using ICP-MS, and then gold as well as silver were detected in the worm. Gold was detected for the first time from marine animals.     

Enhanced removal of lead(II) and cadmium(II) from water in alum coagulation by ferrate(VI) pretreatment.

A laboratory study demonstrated that ferrate pretreatment significantly enhanced lead and cadmium removal in alum coagulation, under the conditions of natural surface water. The enhancement of lead removal was approximately 21 to 37% by ferrate pretreatment at a dosage of 1 to 5 mg/L. The enhanced removal of cadmium by ferrate pretreatment at a dosage of 1 to 5 mg/L exceeded the removal by alum coagulation alone 2-to 12-fold. Cadmium is much more difficult to remove than lead in alum coagulation. The performance of ferrate in enhancing the removal of lead and cadmium in alum coagulation was better than that of ferric chloride. The removal of lead and cadmium was highly pH-dependent, following the general trend of higher pH being related to higher removal. Satisfactory removal of cadmium could be expected by ferrate pretreatment combined with adjusting the pH of the water.     

Partition coefficients of organochlorine pesticides on soil and on the dissolved organic matter in water

The partition coefficients of organochlorine pesticides (OCPs) between the organic matter of Taichung soil and water (K_oc) were evaluated with batch-type experiments. The partition coefficients of OCPs between Aldrich humic acid and water (K_doc) were estimated with solubility enhancement method as well. In this study, the K_ocs of aldrin, heptachlor, and p,p′-DDT are greater than their K_docs, and the relationship of dieldrin and heptachlor epoxide are opposite. The variations of partition coefficients are discussed. For predicting K_doc, a log-log regression relationship of K_doc and K_ow is determined.     

多点源噪声等值线的软件开发

介绍了多点源噪声等直线绘制软件的开发思路与核心代码。     

The influence of pH on the degradation of phenol and chlorophenols by potassium ferrate

This paper presents information concerning the influence of solution pH on the aqueous reaction between potassium ferrate and phenol and three chlorinated phenols: 4-chlorophenol (CP), 2,4-dichlorophenol (DCP), 2,4,6-trichlorophenol (TCP). The redox potential and aqueous stability of the ferrate ion, and the reactivity of dissociating compounds, are known to be pH dependent. Laboratory tests have been undertaken over a wide range of pH (5.8-11) and reactant concentrations (ferrate:compound molar ratios of 1:1 to 8:1). The reactivity of trichloroethylene was also investigated as a reference compound owing to its non-dissociating nature. The extent of compound degradation by ferrate was found to be highly pH dependent, and the optimal pH (maximum degradation) decreased in the order: phenol/CP, DCP, TCP; at the optimal pH the degree of degradation of these compounds was similar. The results indicate that for the group of phenol and chlorophenols studied, the presence of an increasing number of chlorine substituent atoms corresponds to an increasing reactivity of the undissociated compound, and a decreasing reactivity of the dissociated compound.     

氨氮废水处理技术研究进展

氨氮废水是造成水体富营养化的主要因素之一 ,本文综述了氨氮废水的几种主要处理技术 ,介绍了它们的处理原理以及适用条件 ,指出了今后研究工作中需要解决的问题和氨氮废水处理技术今后的发展方向