可吸入尘中苯并（a）芘超声提取的高效液相色谱测定法

本文介绍一种简便、快速的可吸入尘中苯并(a)茈高效液相色谱测定方法.本法仅需5mL乙腈,超声处理10min即可完成提取过程.提取液离心后,上清液可直接进行HPLC分析.色谱条件:反相C18柱,用乙腈/水梯度洗脱,紫外检测器,λ=254nm.方法的最小检出量10~(-10)g.回收率95%,变异系数4、3%.此方法可用于大气可吸入尘中Bap的监测.     

Preliminary evidence for the metabolism of benzo(a) pyrene by Plantago lanceolata

Polycyclic aromatic hydrocarbons (PAHs) have long been recognised as potential carcinogens in animals in which biotransformation into reactive metabolites can lead to DNA damage. In animals PAHs metabolism mainly occurs in hepatic microsomes and is associated with the cytochrome p-450 mediated mixed functional oxidase (MFO) system. PAH metabolism in plants has been shown to occur via a similar enzyme system, but has received relatively little attention. This study is looking at how the plant species Plantago lanceolata metabolises benzo(a)pyrene (B(a)P), which is one of the PAHs whose metabolism has been studied extensively in animals. The aim of the work is to establish firstly that the B(a)P is taken up and secondly that it is biotransformed by the plant to products possibly similar to those found in animals. This work is achieved by using C-14-B(a)P along with whole body autoradiography, scintillation analysis and chromatography techniques to locate the B(a)P and its metabolites.     

Degradation of Benzo[a]Pyrene in Soil with Arbuscular Mycorrhizal Alfalfa

Mycorrhizal and non-mycorrhizal alfalfa (Medicago sativa) was grown in pots containing soil artificially contaminated with various levels of benzo[a]pyrene (B[a]P)(0, 1, 10 and 100 mg kg^–1). Soil and plants were sampled after 30, 40, 50, 60 and 90 days and compared with unlanted pots. The percentage of mycorrhizal root length colonized by Glomus caledoniun was not significantly affected by the addition of B[a]P up to 10 mg kg^–1 but was significantly lower at 100 mg kg^–1B[a]P compared with low concentrations (p < 0.05). There was no difference in soil polyphenol oxidase and dehydrogenase activity among the controls and applications of 1 and 10 mg kg^–1 of B[a]P. However, enzyme activities were significantly higher at 100 mg kg^–1B[a]P compared with the other three treatments, and there was no mycorrhizal effect. Over a period of 90 days the concentration of B[a]P in soil in which alfalfa was grown was significantly lower than in unplanted soil (p < 0.05). Degradation rates of B[a]P added at 1, 10 and 100 mg kg^–1 without G. caledonium were 76, 78 and 53%, and with mycorrhizal inoculation were 86, 87 and 57%. The degradation rate in unplanted soil was significantly lower than in planted soil, and was significantly higher in medium- and low-B[a]P treatments than in the high B[a]P concentration tested. There is a possibility of enhancement phytoremediation of PAHs in rhizosphere soil with arbuscular mycorrhizal fungi.     

荧光猝灭法测定菲、苊、芘与腐殖酸的结合常数

用荧光猝灭法测定了胡敏酸（Fluka）与苊、菲和芘相互作用的结合常数（KDOC），其lgKDOC值分别为4．4，4．48和4．89．用同样方法测得长江水生FA以及黑龙江水生FA和HA的KDOC之间有显著差别．HA的KDODC一般高于FA．黑龙江水生FA的KDOC高于长江．对同一来源的腐殖酸，三种多环芳烃的KDOC与KOW呈线性相关．     

用黄铁矿制备含砷废水净化剂的实验研究

本文报道了以黄铁矿和还原铁粉或其代用品为原料，制备含砷废水净化剂－硫化亚铁的方法。原料配比为１００：３５，粒度≤１００目，反应温度为２００～３５０℃是制备的最佳条件。本法原料广，工艺简单，成本低，具有良好的开发应用前景。     

超塑性恒压充模胀形过程中材料的流动和充填规律

采用刚粘塑性有限元法模拟超塑性恒压充模胀形过程,给出了材料质点的流动轨迹和不同时刻的胀形件剖面形状,分析了模具几何形状参数对单元贴模次序、贴模部位的影响。     

民国初年灾荒史研究综述

自民国迄今,一些政治家、思想家及学者分别从自然科学角度和社会历史角度对民国初年灾荒史予以诠释,依时间而言主要集中于20世纪80年代以后,依内容而言又呈现出一种多元化的态势。其间,虽然取得了一定的成就,诸如积累了一些资料、研究内容多样化等,但仍存在着一些不足。     

大气飘尘中苯并[a]芘的激光诱导荧光法测定

以激光诱导荧光法测定大气飘尘中的苯并[a]芘。方法的检测限为0.01μg·l~(-1),降低了常规荧光法的检测限。综合溶剂提取、柱色层及纸色层分离技术,测定了上海市某些地区大气飘尘样品中苯并[a]芘的含量。     

香港近海海域叶绿素a定量反演及时空变化分析

以2009~2019年HJ-1A/B卫星多光谱数据和对应日期的实测数据为数据源,通过预处理提取出各波段组合反射率并与实测叶绿素a浓度数据进行统计相关性分析,选取相关性最高的波段组合作为特征变量与2/3的实测叶绿素a浓度数据进行建模,并用剩下的1/3实测叶绿素a浓度数据进行精度验证以确定最佳遥感反演模型,最后根据最佳反演模型对2009-2019年的香港近海海域叶绿素a浓度进行反演,明晰该海域近10年的叶绿素a浓度时空变化特征.结果表明：利用HJ-1A/B卫星多光谱数据反演香港近海海域叶绿素a浓度的最佳波段组合为第3波段和第2波段比值（B3/B2）,相关系数（r）为0.893;最佳反演模型为利用B3/B2构建的e指数回归模型（Chl=0.004e^6.693(B3/B2)）,决定系数（R²）为0.934,均方根误差（RMSE）为0.255μg/L,平均相对误差（RPD）为25%;近10年香港近海海域的叶绿素a浓度时空变化特征：空间上整体呈现“东高西低,由东向西逐渐减小”的分布特征,西部海域比东部海域平均浓度低5μg/L左右;2017年内呈“春低秋高,夏升冬降”的随季节变化特点,其中秋季最高,夏春两季次之,冬季最低.     

废弃农药厂拆除过程对周边土壤DDTs污染影响

分4批次分别采集某废弃农药厂拆除前和拆除后周边土壤,研究土壤中DDTs含量、分布和组成的变化特征.结果表明,拆除1个月后,土壤中DDTs残留量（平均为334ng/g）明显大于拆除前（平均为97.0ng/g）,之后土壤中DDTs的残留量明显下降.拆除前,周边土壤中以p,p'-DDE和p,p'-DDD为主,平均浓度分别为35.6和31.0ng/g;拆除后以p,p'-DDT为主要残留污染物,平均浓度为289ng/g,较拆除前（9.69ng/g）增长了28.9倍.来源分析表明,农药厂拆除前周边土壤中DDTs的污染主要受厂区内历史工业品DDTs生产和农田使用的三氯杀螨醇共同影响,而拆除过程周边土壤DDTs污染的贡献主要来自于厂区内工业品DDTs的挥发.在空间分布上,拆除前和拆除后整体上西部区域土壤的污染程度高于东部区域.