速灭菊酯在水稻-水-鱼系统中的动态

采用同位素示踪技术和模拟生态系统试验法,对水田施用速灭菊酯后对邻近水域的污染、水域中鱼类对速灭菊酯残留物的浓缩和排除等进行了研究,结果表明,在田表水中,残留物浓度随处理后时间而迅速降低。水系中淤泥对水中残留物有明显的吸附净化作用,鱼对水中速灭菊酯残留物的摄取和排除均很迅速。 用二室模型对速灭菊酯残留物在田表水中的消失、用一级输入和输出的单室模型对鱼体中残留物浓度随时间的变化动态研究表明,在田表水中,土壤对水中残留物起着强烈的吸附净化作用;在水系中,鱼体中残留物浓度的消长主要取决于残留物自身在水中的消失速率,只是在前期同时依赖于鱼体对残留物的排除效应,鱼体的摄入常数只对鱼体累积浓度最大值及到达最大值的时间T_m产生影响。     

两株假单胞菌对蒽菲芘的降解作用

从污染污泥中分离出两株假单胞菌PCN5及PCB2。研究了它们对蒽、菲、芘的降解性能及生长繁殖情况。结果表明，单基质存在下，10h，PCN5对蒽的降解转化率为91．8％，芘为75．6％，菲仅为26．25％；相反PCB2对菲的降解效果最好，蒽最差；混合基质体系中，两菌株都有良好的降解效果，对芘的降解效果较差；130h，PCN5对蒽、菲、芘混合体系中的TOC去除率为38．9％，PCB2对相应体系的去除率为73．7％；混合体系中两株的生长曲张相似，细菌浓度均呈指数增长趋势，PCN5的最大浓度约是原加入量的10000倍，PCB2是原加入量的8000倍。     

Degradation of Populus euphratica community in the lower reaches of the Tarim River, Xinjiang, China

IntroductionRiparian systems are aquatic-terrestrial ecotones withunique biotic , biophysical and landscape characteristics(Gregory, 1991 ; Naiman, 1997 ; Wiens , 2002) and areshaped by fluvial geomorphic processes . Riparian plantcommunities perform an i…     

镉胁迫下大豆中镉的分布状况及其籽粒品质

溶液培养中0.5μmol·L-1镉胁迫浓度下,大豆表现出轻微受害症状,籽粒减产25 . 7%,而籽粒中粗脂肪和粗蛋白含量变化不大.镉在大豆中的积累分布状况为根>叶>籽>油,比例为32.100:1.690:1.000:0.003.大豆籽粒含镉4.89mg/kg,超过了国家环境标准规定的最高容许量.而大豆粗脂肪中含镉仅0.015mg/kg,远低于国家食品环境卫生标准.豆粕中含镉6.17mg/kg,表明大豆籽粒中的镉主要存在于粗蛋白和淀粉中.     

水中酚类有机污染物HPLC分析及其应用

超声辐照技术降解水中有机污染物，其降解效率的主平价需要简单、快捷和精确的分析方法。为此研究了5种优先控制酚类污染物的HPLC分离及定量分析方法，方法的定量范围为0.4-100mg/L，检测限介于0.34-0.79ng/μL。4－氯酚的超声降解实验表明，随着反应溶液中4－氯酚初始浓度的降低，降解效率明显提高，因此该方法适用于超声降解过程中酚类污染物的跟踪测定。     

不对称氧化铝膜管的微滤性能研究

采用熔模离心法制备的不对称氧化铝微滤膜管的孔径沿径向呈样度分布，控制层孔径均匀。最可几孔径为０．０５μｍ，最大孔径为０．１μｍ的管能滤原液中全部的细菌，获得完全无菌的水，但过滤速率太慢，最可几孔径为０．１μｍ，最大孔径为０．２μｍ、最大孔径０．３μｍ。     

我国SO_2和NO_X排放强度地理分布和历史趋势

根据我国燃料消费、燃料的含硫量和硫与氮氧化物排放因子，计算我国各地区ＳＯ_２和ＮＯ_Ｘ排放强度地理分布。结果指出，我国原煤含硫量为１．１２％。１９９０年全国ＳＯ_２和ＮＯ_Ｘ的排放量分别为１７５１．８万ｔ和８４２．２万ｔ，排放强度最大的地区是中东部地区，即辽宁、河北、山东、山西和浙江。这些地区平均排放强度大于７ｔ／ｋｍ￣２·ａ。还估算了全国１９５０～１９９０年ＳＯ_２和ＮＯ_Ｘ历年的排放量。     

泸沽湖沉积物－水界面扩散作用对上覆水体基本化学组成的影响

通过云南泸沽湖－－半封闭深水湖泊湖水和沉积物孔隙中Ｃａ＾２＋、Ｋ＾＋、Ｎａ＾＋、ＨＣＯ３等基本组分及ＰＨ等剖面分布的研究，结果表明，这些基本组分可以自底部沉积物向上覆体扩散迁移，定量地估算了扩散通量及其对上覆水体的影响程度，说明湖泊沉积物－水界面作用在控制整个水体水化学基本组成中的起着重要的作用。     

Adsorption selectivity of salicylic acid and 5-sulfosalicylic acid onto hypercrosslinked polymeric adsorbents

Both bottle-point and column-feeding experiments involving different solutes and sorbents were carried out to investigate the adsorption selectivity and separation performance of salicylic acid and 5-sulfosalicylic acid. Their adsorption isotherms onto such hypercrosslinked polymeric adsorbents as NDA-100 and NDA-99 could be well described by the Freundlich equations whose characteristics describe extrathermic and favorable adsorption processes. The adsorption towards NDA-100 mainly depended on the π-π interaction, while that towards NDA-99 was extremely influenced by the static-electric interaction. Additionally, the adsorptive capacity of salicylic acid on NDA-99 decreased while it increased on NDA-100 with the presence of 5-sulfosalicylic acid in the adsorptive environment as the competitive component. Comparatively, the adsorption capacity of 5-sulfosalicylic acid decreased on both resins with salicylic acid as the competitive component. In fact, the difference in the interaction between adsorbent and adsorbate resulted in the straight antagonism on the effective adsorption sites on the adsorbent. In conclusion, the adsorption selectivity of salicylic acid onto NDA-100 was obviously larger than that onto NDA-99 with the existence of 5-sulfosalicylic acid in the adsorptive environment. A satisfactory separation and recovery of tested solutes in aqueous phase could be foreseeably achieved by the sequencing adsorption technique involving NDA-100 as well as NDA-99. Translated from Environmental Pollution & Control, 2005, 27(8): 570–574 [译自: 环境污染与防治]