2011年春季辽宁一次沙尘天气过程及其对不同粒径颗粒物和空气质量的影响

利用2011年5月11—12日辽宁沙尘天气过程的相关资料,分析了沙尘天气对不同粒径颗粒物及空气质量的影响及此次沙尘过程的天气成因.结果表明:沙尘天气发生前后可吸入颗粒物PM₁₀、PM_2.5和PM₁的浓度变化很大,沈阳、鞍山、本溪和丹东4城市PM₁₀、PM_2.5的小时浓度最大值都增大了1.5~20倍;粗粒子PM_(2.5~10)的数量浓度分别增加了30~41倍,质量浓度分别增加了27~30倍;细粒子PM_(1~2.5)的质量浓度分别增加了30~35倍,数量浓度分别增加了15~30倍;微粒子的数量浓度和质量浓度各城市表现不同,沈阳微粒子的数量浓度和质量浓度最大值增大了3倍和5倍,而鞍山PM₁的数量浓度和质量浓度分别减少了50%和10%.受蒙古气旋的影响内蒙古地区产生大风降温天气,大风将内蒙古地区的沙尘带到高空并随西风带向东移动进入辽宁,由于辽宁地区风速比较小,造成了辽宁大部分地区的浮尘天气,并对辽宁各地空气质量造成了严重影响,除丹东外辽宁其他13个城市空气质量都达到了轻微污染到重度污染的级别,铁岭、阜新、沈阳和抚顺的污染指数分别超过了300,达到了重度污染的级别.     

牡丹江流域水质变化趋势及水环境污染特征研究

通过对牡丹江近10年水质监测、评价及变化趋势研究,采用单项污染指数评价法、环境功能区达标评价法,评价牡丹江丰水期、平水期、枯水期水质现状,给出超标项目与超标倍数,计算污染分担率、污染负荷比,绘制主要污染物各断面浓度变化图,总结牡丹江污染特点和水质变化趋势,得出牡丹江水环境污染特征,为环境管理提供科学依据。     

Distribution of heavy metals in sediments of the Pearl River Estuary, Southern China: Implications for sources and historical changes

The distribution of heavy metals (Pb, Zn, Cd and As) in sediments of the Pearl River Estuary was investigated. The spatial distribution of heavy metals displayed a decreasing pattern from the turbidity maxima to both upstream and downstream of the estuary, which suggested that suspended sediments played an important role in the trace metal distribution in the Pearl River Estuary. In addition, metal concentrations were higher in the west part of the estuary which received most of the pollutants from the Pearl River. In the sediment cores, fluxes of heavy metals were consistent with a predominant anthropogenic input in the period 1970-1990. From the mid-1990s to the 2000s, there was a significant decline in heavy metal pollution. The observed decline has shown the result of pollution control in the Pearl River Delta. However, it is noteworthy that the metal concentrations in the most recent sediment still remained considerably high. Taken together, the enrichment of heavy metals in sediments was largely controlled by anthropogenic pollution.     

滇池流域土壤活性腐殖质及其主要组分的紫外-可见与三维荧光光学特性

利用紫外-可见光谱和三维荧光光谱技术,结合土壤腐殖质及腐殖质组分(胡敏酸、富里酸)中的有机碳含量,研究了滇池流域土壤活性腐殖质及其组分胡敏酸和富里酸的光谱特征.结果表明,滇池流域土壤活性腐殖质中富里酸含量高于胡敏酸,流域范围内土壤活性腐殖质及其组分含量分布不均匀,活性腐殖质、胡敏酸和富里酸含量的变异系数分别达37.7%、36.4%、40.9%.土壤活性腐殖质及其组分胡敏酸和富里酸的碳含量均表现为菜地荒地草地湿地.光谱特征结果表明,滇池流域土壤活性腐殖质主要由自生源物质和经一定程度降解后的外源物质共同组成.此外,自生源性与光化学及生物活性具有正相关关系.因此,具有弱自生源性的滇池流域土壤活性腐殖质所具有的光化学和生物活性较弱.     

化学解耦联剂对活性污泥工艺中污泥产率的影响

采用3,3′,4′,5-四氯水杨酰苯胺(TCS)作为代谢解耦联剂添加到活性污泥工艺中,连续曝气分批培养实验结果表明,TCS在浓度高于1.0mg/L时是一种有效的化学解耦联剂,能显著地降低污泥产率.当TCS浓度为6.0mg/L时,污泥产率可降低约50%.在40d的运行期间,隔天分别在3个反应器中添加TCS 2.0、2.8和3.6mg/L,基质的去除能力和出水氨氮及总氮浓度均未受影响,污泥的SOUR值和脱氢酶活性相应增加,污泥的沉降性能也未见有明显影响.镜检发现,对照反应器中的污泥经40d运行后仍有丝状菌存在,而添加解耦联剂反应器中的污泥几乎无丝状菌的存在.以上结果表明,可以应用TCS来降低活性污泥工艺中的剩余污泥产量.     

防止井下作业污染环境的工艺技术应用

分析了井下作业施工对环境造成污染的因素，介绍江苏油田在井下作业过程中进行污染防治的措施及其相关配套新工艺、新技术的应用和效果。     

Analysis of relationship between economic growth and environment in Benxi Shiqiaozi Development Zone

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Soil C and N models that integrate microbial diversity

Industrial agriculture is yearly responsible for the loss of 55–100 Pg of historical soil carbon and 9.9 Tg of reactive nitrogen worldwide. Therefore, management practices should be adapted to preserve ecological processes and reduce inputs and environmental impacts. In particular, the management of soil organic matter (SOM) is a key factor influencing C and N cycles. Soil microorganisms play a central role in SOM dynamics. For instance, microbial diversity may explain up to 77 % of carbon mineralisation activities. However, soil microbial diversity is actually rarely taken into account in models of C and N dynamics. Here, we review the influence of microbial diversity on C and N dynamics, and the integration of microbial diversity in soil C and N models. We found that a gain of microbial richness and evenness enhances soil C and N dynamics on the average, though the improvement of C and N dynamics depends on the composition of microbial community. We reviewed 50 models integrating soil microbial diversity. More than 90 % of models integrate microbial diversity with discrete compartments representing conceptual functional groups (64 %) or identified taxonomic groups interacting in a food web (28 %). Half of the models have not been tested against an empirical dataset while the other half mainly consider fixed parameters. This is due to the difficulty to link taxonomic and functional diversity.     

Catalytic activities and mechanism of formaldehyde oxidation over gold supported on MnO<Subscript>2</Subscript> microsphere catalysts at room temperature

MnO₂ microspheres with various surface structures were prepared using the hydrothermal method, and Au/MnO₂ catalysts were synthesized using the sol-gel method. We obtained three MnO₂ microspheres and Au/MnO₂ samples: coherent solid spheres covered with wire-like nanostructures, solid spheres with nanosheets, and hierarchical hollow microspheres with nanoplatelets and nanorods. We investigated the properties and catalytic activities of formaldehyde oxidation at room temperature. Crystalline structures of MnO₂ are the main factor affecting the catalytic activities of these samples, and γ-MnO₂ shows high catalytic performance. The excellent redox properties are responsible for the catalytic ability of γ-MnO₂. The gold-supported interaction can change the redox properties of catalysts and accelerate surface oxygen species transition, which can account for the catalytic activity enhancement of Au/MnO₂. We also studied intermediate species. The dioxymethylene (DOM) and formate species formed on the catalyst surface were considered intermediates, and were ultimately transformed into hydrocarbonate and carbonate and then decomposed into CO₂. A proposed mechanism of formaldehyde oxidation over Au/MnO₂ catalysts was also obtained.