福建省海岸带土壤环境背景值研究及其应用

本文采用《福建省土壤环境背景值研究》课题的有关资料，研究福建省海岸带土壤主要元素背景值，讨论其主要影响因素，并应用来对福建省海岸带陆地土壤质量进行评价。     

中国污染场地管理面临的问题及对策

概述了欧美国家污染场地管理现状,分析了中国污染场地管理面临的突出问题:中国在污染土壤管理的法律法规和标准、污染土壤的修复技术、污染土壤治理投入等方面同欧美国家有一定的差距.结合污染场地管理和场地风险评估、场地修复条件以及土地利用功能,提出了基于风险评估基础上污染场地管理程序和污染场地管理亟待开展的工作.指出了土壤环境标准体系,污染场地管理体系和污染场地修复技术体系的三元结构的完善是破解中国污染场地管理和修复的难题的根本.     

大庆油田落地原油对土壤污染的研究

大庆油田是中国最重要的原油生产基地,开发建设50多年来,已累计生产原油18.2亿吨.不可避免地在油田生产过程中产生大量的落地原油,对土壤造成了严重的污染.落地原油在土壤中的迁移主要有横向迁移和纵向迁移:横向迁移对土壤的污染成辐射状分布,污染强度随污染源的距离增加而迅速降低,污染源周围污染最重的区域在0 m～40 m范围内,占总量90%以上,横向迁移范围确定在150 m以内;落地原油纵向迁移绝大部分集中在距土壤表面0 cm～10 cm范围内,竖向迁移一般不超过70 cm.落地原油污染土壤中主要污染物包括总烃、芳烃、酚、苯并[a]芘和硫化物,通过落地原油污染土壤的模拟实验可知总烃、芳烃、苯并[a]芘和硫化物含量,随原油浓度增加而明显增加,呈明显正相关性;其一元线性回归方程分别为Y=0.470X-17.88、Y=0.119X-6.13、Y=0.0076X-0.30、Y=0.000055X 0.089.     

桂林市某蔬菜种植基地重金属污染调查及分析

通过对桂林市某蔬菜种植基地灌溉水、土壤与蔬菜中重金属的测定,结合国家农灌水、土壤和食品卫生标准,分析了该区Cu、Pb、Zn、Cd污染状况。经测定分析,该区灌溉水质达到了国家三类水质标准;土壤中重金属含量普遍超过背景值,但达到了国家土壤环境质量标准;蔬菜中的重金属含量符合国家无公害蔬菜的标准。结果表明,该区尚未受到重金属污染,符合无公害食品种植基地要求。     

蚯蚓-菌根相互作用对土壤-植物系统中Cd迁移转化的影响

以灰化土(Aquods soil)为供试土壤,分别加入4种含量的Cd2 (0、5、10、20 mg·kg-1)模拟土壤污染,设置单独加8条蚯蚓(Pheretima sp.)、单独接种菌根(Inoculum Endorize-Mix2)、同时接种蚯蚓和菌根的3种处理,以不加蚯蚓和菌根为对照,各处理均种植黑麦草(Lolium multiflorum),研究蚯蚓、菌根相互作用对土壤-植物系统中Cd迁移转化的影响.结果表明:(1)菌根对土壤pH无明显影响,加蚯蚓可使土壤pH比对照约降低0.2,蚯蚓和菌根同时作用对土壤pH降低没有协同作用.(2)蚯蚓或菌根的加入均能显著增加土壤中可溶性有机碳(DOC)含量,蚯蚓的影响大于菌根,同时加入蚯蚓和接种菌根对土壤中DOC的增加有一定的拮抗作用.(3)蚯蚓活动增加了黑麦草根部Cd的积累,菌根则能促进Cd从黑麦草根部向地上部转移,二者具有促进Cd向地上部分转移的协同作用.(4)蚓粪和土壤中DTPA提取态Cd含量与黑麦草吸收Cd量呈显著相关(p＜0.01),而蚓粪中DTPA提取态Cd含量均显著高于土壤中的含量(p＜0.05).因此,蚓粪中有效态Cd是植物吸收Cd的重要供源.     

无锡市桃花山生活垃圾填埋场扩建工程渗沥液导排设计

通过分析无锡市桃花山垃圾填埋场原工程渗沥液导排在实际运行中存在的问题,针对当前卫生填埋场的现状,提出扩建工程在原工程和扩建工程和新场渗沥液导排2个关键环节上采取的措施。     

影响土壤重金属生物毒性的若干因子

本文应用发光细菌法探讨了土壤类型、粘土矿物、无定形金属氧化物、吸附剂对重金属纯溶液以及重金属污染土壤的降毒效应.红壤、砖红壤对Cu、Cd、Pb呈现负的降毒效应,而对As具有明显的降毒作用.黑土、黄棕壤对供试阳离子金属具有明显的降毒效应,对As降毒却不明显.试验证明粘土矿物及其组成是影响土壤重金属毒性的最基本因素.无定形氧化锰对供试阳离子金属的降毒能力大于无定形氧化铁,对As的效应二者则相反.不同吸附剂对Cu、Cd、Pb呈现基本相同的降毒顺序,即炉烟灰>活性炭>泥炭>干活性污泥,不同配比吸附剂对红壤添加性阳离子和东乡铜矿污染土壤均具有明显的降毒作用.添加吸附剂的东乡铜矿污染土壤随着土壤溶液毒性的消除,随之也消除或减轻了其对水稻种芽的急性毒害.     

Uncommon chromosomal mosaicism in chorionic villi

Three cases of unusual chromosomal mosaicism are reported for which the cytogenetic data show inconsistent findings between CVS and AC or fetal tissue, and which cannot be explained simply by non-disjunction. For case 1, in CVS the karyotype was 46,XY, whereas lymphocytes and fibroblasts revealed 69,XXY. DNA fingerprinting indicated one paternal and two maternal chromosome sets, the latter most probably due to omission of maternal meiosis II. For case 2, in CVS mos 46,XX/47,XX,+mar de novo was observed. Amniotic fluid cells had the karyotype 46,XX. The origin of the marker chromosome might be explained by at least two events of unknown order (a somatic chromosome/chromatid deletion and non-disjunction of the homologous chromosome). In case 3 (CVS: mos 46,XY/46,XY,19q+ de novo; amniotic fluid cells, lymphocytes, and fibroblasts: 46,XY), the surplus of chromosome material in 19q+ might be explained on the basis of a somatic translocation. The idea of a chimera is less convincing, as the mosaic finding is restricted to one tissue. Furthermore, there was no hint of a vanishing twin. Hitherto, no case of structural chromosome mosaicism in CVS has been reconfirmed in fetal tissues.     

First-trimester prenatal diagnosis in quintuplets: A practical approach using step-by-step embryo reduction

A multiple pregnancy of high rank may occur in a couple at risk for a Mendelian disorder. Prenatal diagnosis is hampered by the difficulty of (1) obtaining chorionic villi from each zygote arid (2) unequivocally relating each sample to the corresponding embryo. The calculation of the genetic risk according to the number of zygotes led us to propose a diagnostic strategy based on embryo reduction, a technique initially designed to improve the perinatal outcome of multiple pregnancies with normal embryos. We report a case in which this approach allowed rational use of first-trimester chorionic villus sampling in a quintuplet pregnancy at risk for non-ketotic hyperglycinaemia, resulting in the selective birth of unaffected twins.     

Prenatal diagnosis of Chediak-Higashi syndrome

We report the first prenatal diagnosis of an affected fetus with Chediak-Higashi syndrome (CHS). Diagnosis was accomplished via fetal blood sampling at 17 menstrual weeks and was confirmed after birth. Retrospective measurement of the largest acid phosphatase-positive lysosomes in cultured amniotic fluid cells and chorionic villus cells showed that in CHS these lysosomes are significantly larger than those in normal cells. This method may be used for prenatal diagnosis of CHS by amniocentesis and chorionic villus sampling (CVS).