神农架主峰南坡猕猴桃种质资源调查及保护策略

巴东县北部神农架主峰南坡的送子园原始森林保护区内具有种类繁多的猕猴桃种质资源，经调查发现共分布有中华猕猴桃（A.chiensis)、美味猕猴桃（A.deliciosa)、革叶猕猴桃(A．rubricalis var.coriacea)、葛枣猴桃(A．ploygama)、京梨猕猴桃(A．callosa var．henryi)、软枣猕猴桃(A．arguta)、巴东猕猴桃(A．tetramera var.badongenisis)、紫果猕猴桃(A．arguta var.purpurea)及紫果新变型、绵毛藤山柳(Clematoclthra lanosa)10种(包括变种、变型)。简述了各种类的植物学性状和果实经济性状，种质资源分布的主要特点以及生态环境，指出由于砍伐森林和环境条件的恶化使猕猴桃资源已受到威胁和破坏，提出保护策略的重点是提高全民的生态保护意识；可持续开发利用资源；加大科技对猕猴桃资源保护支撑的力度。其主要保育措施：一是在保护区内就地进一步加强物种全面保护；二是省级以上科研单位分区建立猕猴桃后种质资源圃，对濒危物种或持有物种进行迁地保护；三是开展超低温保存技术的研究，建立种子和花粉基因库。并建立完善与国际接轨的信息数据库平台，便于国际合作与交流。     

长江三峡地区坡地发育初步研究

坡地发育是地貌学研究的基本问题之一。三峡地区坡地发育的研究对三峡库岸稳定性的评估和三峡移民的土地开发具有十分重要的意义。首先从概括坡地发育的研究进展，阐述科学家们对坡地发育的不同看法入手，引出三峡地区坡地发育的特殊性。初步研究三峡地区的坡地发育具有分段式分进的特点，包括中山峰陡坡的剥蚀后退过程，山顶缓坡的风化剥蚀夷平的过程，上段斜坡的片流坡地侵蚀过程，下段陡坡的剥坡后退过程，山麓堆积缓坡的剥蚀过程等。通过分析三峡地区坡地的五种坡段的成因、现状、发展趋势以及它们对三峡库区的稳定性和三峡移民的土地开发的影响，预测未来的三峡库岸，大部分为剥蚀陡坡，部分为崩塌滑坡陡坡，三峡沿岸城镇开发建设的重点将是库岸有坡地的防护工程。     

Active capping demonstration in the Anacostia river,Washington, D.C.

An active capping demonstration project in Washington, D.C., is testing the ability to place sequestering agents on contaminated sediments using conventional equipment and evaluating their subsequent effectiveness relative to conventional passive sand sediment caps. Selected active capping materials include: (1) AquaBlokTM, a clay material for permeability control; (2) apatite, a phosphate mineral for metals control; (3) coke, an organic sequestration agent; and (4) sand material for a control cap. All of the materials, except coke, were placed in 8,000‐ft test plots by a conventional clamshell method during March and April 2004. Coke was placed as a 1.25‐cm layer in a laminated mat due to concerns related to settling of the material. Postcap sampling and analysis were conducted during the first, sixth, and eighteenth months after placement. Although postcap sampling is expected to continue for at least an additional 24 months, this article summarizes the results of the demonstration project and postcap sampling efforts up to 18 months. Conventional clamshell placement was found to be effective for placing relatively thin (six‐inch) layers of active material. The viability of placing high‐value or difficult‐to‐place material in a controlled manner was successfully demonstrated with the laminated mat. Postcap monitoring indicates that all cap materials effectively isolated contaminants, but it is not yet possible to differentiate between conventional sand and active cap layer performance. Monitoring of the permeability control layer indicated effective reductions in groundwater seepage rates through the cap, but also showed the potential for gas accumulation and irregular release. All of the cap materials show deposition of new contaminated sediment onto the surface of the caps, illustrating the importance of source control in maintaining sediment quality. © 2006 Wiley Periodicals, Inc.     

Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families

Childhood-onset spinal muscular atrophy (SMA) is one of the most common neurodegenerative genetic disorders. SMN1 is the SMA-determining gene deleted or mutated in the majority of SMA cases. There is no effective cure or treatment for this disease yet. Thus, the availability of prenatal testing is important. Here we report prenatal prediction for 68 fetuses in 63 Turkish SMA families using direct deletion analysis of the SMN1 gene by restriction digestion. The genotype of the index case was known in 40 families (Group A) but unknown in the remaining 23 families (Group B). A total of ten fetuses were predicted to be affected. Eight of these fetuses were derived from Group A and two of these fetuses were from Group B families. Two fetuses from the same family in Group A had the SMNhyb1 gene in addition to homozygous deletion of the NAIP gene. One fetus from Group A was homozygously deleted for only exon 8 of the SMN2 gene, and further analysis showed the presence of both the SMN1 and SMNhyb1 genes but not the SMN2 gene. In addition, one carrier with a homozygous deletion of only exon 8 of the SMN1 gene was detected to have a SMNhyb2 gene, which was also found in the fetus. To our knowledge, these are the first prenatal cases with SMNhyb genes. Follow-up studies demonstrated that the prenatal predictions and the phenotype of the fetuses correlated well in 33 type I pregnancies demonstrating that a careful molecular analysis of the SMN genes is very useful in predicting the phenotype of the fetus in families at risk for SMA. Copyright © 2002 John Wiley & Sons, Ltd.     

A closed-chamber CO2-flux method for estimating intertidal primary production and respiration under emersed conditions

This paper describes a closed-chamber method for measuring CO₂ fluxes in intertidal soft sediments during periods of emersion. The method relies on closed-circuit incubations of undisturbed sediment and measurement of CO₂ exchanges using an infrared gas analyser. The method was assessed during field experiments, both in light and dark conditions, on an exposed sandy beach and in an estuary. The rates of gross community production measured under moderate irradiance (4.2 mg C m^-2 h^-1 on the exposed sandy beach and 35 mg C m^-2 h^-1 in the estuary) are in good agreement with rates reported in the literature. In conjunction with appropriate sampling strategies, this method can be useful for estimating and comparing production of intertidal areas or for assessing factors that influence production.     

电感耦合等离子体质谱法在环境监测中的应用

针对ICP-MS技术的使用特点及其近年来在环境监测领域的应用进行综合阐述，并对ICP-MS技术的发展前景作出简单的评述。     

乡镇工业污染防治战略初探

本文通过对乡镇工业经济发展现状及其环境问题的评价分析,提出乡镇工业环境管理应按本地自然条件、经济发展水平和乡镇企业的特点,实施分区域、按行业、有重点地进行管理的防治战略。并建议我国环境管理在以城市和大工业为重点的同时,及早将乡镇工业污染防治工作放在战略高度加以重视,切实加强乡镇工业环境管理。     

A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis

The presence of maternal cells in fetal samples constitutes a serious potential source for prenatal misdiagnosis. Here we present our approach for detecting maternal cell contamination (MCC) at prenatal diagnosis for eight monogenic disorders (autosomal recessive: β-thalassaemia, sickle-cell anaemia, cystic fibrosis, prelingual deafness; autosomal dominant: achondroplasia, Huntington disease, myotonic dystrophy, neurofibromatosis type I; X-linked: spinobulbar muscular atrophy). Our aim was to apply a simple and low-cost approach, which would easily and accurately provide information on the fetal tissue MCC status. MCC testing was applied to cases of recessive inheritance where the primary mutation screening of the fetus revealed the presence of the maternal mutation, to cases concerning dominant inheritance and to cases of multiple gestation. The potential presence of maternal cells was determined by the amplification of the 3′-HVR/APO B, D1S80, THO1 and VNTRI of vWf polymorphic loci, which have previously demonstrated high heterozygosity in Caucasians. Among 135 prenatal diagnoses, 44 finally needed to be tested for MCC (32.6%). MCC was detected in four cases, where DNA was isolated directly from chorionic villi samples (CVS), and in one case with DNA isolated directly from amniotic fluid (AF). In almost 90% of cases a simple test of one polymorphic locus provided sufficient information about MCC. The choice of the appropriate locus is therefore essential, while the simultaneous screening of both parents provides the means for distinguishing non-informative sites about MCC. Copyright © 2002 John Wiley & Sons, Ltd.