模拟氮沉降对苗圃地土壤动物群落的影响

通过人工喷施氮H4NO3建立了一个模拟氮沉降增加梯度系列,在近18个月的试验处理期间,研究了2003年7月、10月和2004年2月、5月这几个不同季度苗圃试验样地土壤动物群落对氮沉降增加的响应。实验分为5个处理组:对照、低氮、中氮、高氮和倍高氮,分别接受0、5、10、15、30g/(m2·a)的氮沉降量。土壤细菌和真菌的数量总体上随氮处理的加强而持续显著地增长,土壤有机氮含量也持续升高,土壤酸度则不断下降。采样期对土壤动物的个体数量、类群丰度和多样性存在显著的影响,总的来说,土壤动物群落随试验处理期加长而持续增长。土壤动物群落具有显著的垂直分异特征,土壤I层土壤动物个体数量、类群丰度和多样性显著高于II和III层。氮沉降增加对土壤动物群落有明显的影响,表现为施氮处理明显有利于土壤动物群落的发展,但也具有明显的阀值效应。与对照样地相比,各施氮处理样地土壤动物群落水平整体为高,而且随试验处理时间的增加这种差异有加大的趋势;氮沉降增加处理与取样期之间存在显著的交互作用,除了2月取样,中氮处理土壤动物群落水平都处于最高水平,而对照处理一般处于最低水平,这种趋势在最后一次取样中最为明显;氮沉降处理与土壤动物的垂直分布之间也有明显的交互作用:在土壤I层,从对照至倍高氮处理,土壤动物群     

水质对UV/H_2O_2降解2,4-二氯酚的影响

研究了UV/H2O2工艺对2,4-二氯酚(2,4-DCP)的去除效果和水中阴离子、腐殖酸对该工艺降解2,4-DCP的影响。结果表明:UV/H2O2工艺可以有效的去除水中2,4-DCP,光降解过程符合一级反应动力学模型;在H2O2投加量为8mg/L,1个30W低压汞灯照射下,2,4-DCP在蒸馏水和自来水中光降解速率常数分别为0.0232/min和0.0162/min;NO3-、Cl-、HCO3-对2,4-DCP光降解有抑制作用;当3种离子浓度为0.5mmol/L、10mmol/L、20mmol/L时,对2,4-DCP光降解的抑制程度为HCO3->NO3->Cl-;随着离子浓度增大,抑制作用增强;自来水中的光降解速率常数低于蒸馏水中的光降解速率常数是由于水中多种离子影响的结果;腐殖酸在低浓度时,促进光降解反应的进行,在高浓度时,2,4-DCP的光降解氧化受到抑制。     

2000年环保战略目标定量考核方法研究

参加国家环保局科技3项费用课题《2000年环境保护战略目标定量考核指标研究》的8个地区对于2000年环保战略目标提出了不同的考核方法.本文在深入分析各种考核方法的基础上,通过归纳总结,向读者推荐几种基本方法,它们是 TOPS(?)S 方法、简单加性加权法和公式计分法.这些方法是一些基本的数学手段,通过对各具体考核指标的适当综合,归纳出表征总体目标实现程度的数值.即:这些方法是整体考核方法,从整体上说明存在问题和差距,为决策者提供实现环保战略目标的科学依据.     

Formation of polychlorobiphenyls in silicone rubber

In silicone rubber crosslinked with bis(2,4-dichlorobenzoyl) peroxide (DCBP) as initiator about 0.1% of DCBP is converted into polychlorobiphenyls (PCBs). The PCB content in silicone rubber determined by high resolution gas chromatography (HRGC) after its destruction by HF is around 10 mg/kg. 29 PCB congeners were detected. Instead of the expected PCB-47, lower chlorinated congeners are predominant. Some possible pathways of their origin are presented.     

一种新型复合球填料在低浓度污水再生回用中的应用研究

新型复合球填料为沸石与悬浮球填料的有机组合体,密度约为0.92～0.97g/cm3,比表面积为711～1185m2/m3,表面粗糙,物化性能稳定.在曝气量为20∶1,停留时间为6 h时,装有新型复合球填料的反应柱挂膜容易,成膜时间短,膜不易脱落,且生物相丰富.膜成熟时对生活污水中的氨氮和COD都有很好的去除效果,出水氨氮浓度≤2 mg/L,去除率≥93%;出水COD浓度≤22 mg/L,去除率≥80%.新型复合球反应柱在稳定状态处理低浓度的二级出水时,出水氨氮浓度≤2 mg/L,去除率≥89%,出水COD浓度为10～36 mg/L,去除率为48%～81%.出水水质符合GB50335-2002标准.     

Study of oil-water partitioning of a chemical dispersant using an acute bioassay with marine crustaceans

The toxicity of seawater dispersions of a chemical dispersant to two marine crustaceans was investigated in the presence and absence of various quantities of a non-toxic mineral oil. From the results and a physical-chemical partitioning analysis, a limiting value of the oil-water partition coefficient of the toxic compounds is deduced suggesting that essentially all of the toxic compounds in the dispersant will partition into solution in water following dispersant application to an oil spill. This conclusion simplifies interpretation and prediction of the toxic effects of a dispersed oil spill.The combined bioassay-partitioning procedure may have applications to the study of the toxicity of other complex mixtures such as industrial effluents.     

Widespread contamination by tris(4-chlorophenyl)methane and tris(4-chlorophenyl)methanol in cetaceans from the North Pacific and Asian coastal waters

For understanding global distribution, transport and behavior of tris(4-chlorophenyl)methane (TCPMe) and tris(4-chlorophenyl)methanol (TCPMOH), the two newly identified microcontaminants, the present study determined their concentrations and other persistent organochlorines (OCs) in the blubber of nine species of adult male cetaceans collected from various locations in the North Pacific Ocean and coastal waters of some Asian countries, during 1985-97. Concentrations of TCPMe and TCPMOH were found to be highest in northern right whale dolphins, which may be attributable to wide distribution of this species, including some heavily polluted areas such as coastal California. Elevated residue levels of TCPMe and TCPMOH were observed in both off-shore and coastal species, suggesting widespread contamination of these compounds in the marine environment. Higher contamination of TCPMe and TCPMOH was found in cetaceans from temperate and cold waters than those from tropical regions. The latitudinal distribution of TCPMe and TCPMOH in cetaceans from the North Pacific and Asian coastal waters was similar to that of DDTs, suggesting less transportable nature of TCPMe and TCPMOH in the marine environment. Data on the occurrence of TCPMe and TCPMOH further indicated high bioaccumulation potential of these compounds, which was comparable to DDTs. Relative concentrations of TCPMe/TCPMOH in cetaceans were apparently higher than those observed in seals, suggestive of lower metabolic capacity for these compounds in cetaceans than in pinnipeds, which is similar to classic contaminants like polychlorinated biphenyls and DDTs.     

Baseline study of methane emission from open digesting tanks of palm oil mill effluent treatment

Anthropogenic release of greenhouse gases, especially CO₂ and CH₄ has been recognized as one of the main causes of global warming. Several measures under the Kyoto Protocol 1997 have been drawn up to reduce the greenhouse gases emission. One of the measures is Clean Development Mechanisms (CDM) that was created to enable developed countries to cooperate with developing countries in emission reduction activities. In Malaysia, palm oil industry particularly from palm oil mill effluent (POME) anaerobic treatment has been identified as an important source of CH₄. However, there is no study to quantify the actual CH₄ emission from the commercial scale wastewater treatment facility. Hence, this paper shall address the CH₄ emission from the open digesting tanks in Felda Serting Hilir Palm Oil Mill. CH₄ emission pattern was recorded for 52 weeks from 3600 m³ open digesting tanks. The findings indicated that the CH₄ content was between 13.5% and 49.0% which was lower than the value of 65% reported earlier. The biogas flow rate ranged between 0.8 l min⁻¹ m⁻² and 9.8 l min⁻¹ m⁻². Total CH₄ emission per open digesting tank was 518.9 kg day⁻¹. Relationships between CH₄ emission and total carbon removal and POME discharged were also discussed. Fluctuation of biogas production was observed throughout the studies as a result of seasonal oil palm cropping, mill activities, variation of POME quality and quantity discharged from the mill. Thus only through long-term field measurement CH₄ emission can be accurately estimated.     

Metabolism of the herbicide chlortoluron by human cytochrome P450 3A4

Studies were carried out to investigate the metabolism of herbicide chlortoluron in the microsomal fractions and whole cells of Saccharomyces cerevisiae expressing human cytochrome P450 3A4. Both whole cells and microsomal fractions of yeast expressing human cytochrome P450 3A4 exhibited a typical dithionite-reduced, CO-difference absorbance spectrum with maximum absorbance at 448 nm. Chlortoluron produced a type I binding spectrum with cytochrome P450 3A4 with a K_s value of 200 μM. Chlortoluron was metabolised into four metabolites; hydroxylated-N-monodemethylated, hydroxylated ring methylated, N-didemethylated and N-monodemethylated products. Chlortoluron metabolism was absolutely dependent on NADPH and no metabolism was observed in control transformants.     

Dechlorination of 1,2,4-trichlorobenzene in the sediment of Ise Bay

The relation between dechlorination activities of 1,2,4-trichlorobenzene and anaerobic microbial activity were studied in the sediment collected at three sites in Ise Bay in Japan. The degradation rate of spiked 1,2,4-trichlorobenzene (3nmol ml⁻¹) ranged from 15 to 35 pmol day⁻¹ ml⁻¹ wet sediment and about 1/3 to 1/2 of degraded the trichlorobenzene was recovered as dechlorinated products. Among the dichlorobenzenes, the 1,2-isomer had the highest and 1,3-isomer had the lowest production rate. Comparing the three sampling sites, the trichlorobenzene degradation and dichlorobenzenes production rates were related to the sulfate reducing activity for the unit number of sulfate reducing bacteria. Production rates of dichlorobenzenes were completely inhibited by adding molybdate (20 mM), nitrate (60 mM), and formaldehyde solution (4 %). These results indicated that dechlorination activity in the Ise Bay sediment was supported by sulfate reduction activity in the sediment, and not supported by any other anaerobic microbial activity.