湘东丘陵区不同类型土壤活性碳组分的剖面分布与差异

土壤活性碳组分是土壤健康变化的指示器。选取湘东丘陵区3种不同母质发育的林地土壤（紫色土、板岩红壤和花岗岩红壤）,研究土壤颗粒有机碳（POC）和溶解性有机碳（DOC）的剖面分布规律,并分析POC、DOC与土壤有机碳（SOC）、土壤质地的关系。结果表明：土壤剖面POC、DOC质量分数分别介于0．29～3．87g·kg。和15．01～311．34mg·kg^-1,随剖面加深而大幅降低。土壤剖面POC储量介于8．61一16．54t·hm^-2,以花岗岩红壤最高,板岩红壤最低;而DOC储量介于380．76～1184．83kg·hm^-2,以板岩红壤最高,紫色土最低。POC占SOC的比例（POC／SOC）介于6．42％～46．25％,其中紫色土和板岩红壤POC／SOC随土层加深而降低,而花岗岩红壤则完全相反。DOC占SOC的比例（DOC／SOC）介于O．35％～3．02％,其中紫色土DOC／SOC随土层加深而降低,板岩红壤与花岗岩红壤DOC／SOC则以B层最高。由此可见,不同母质发育的土壤类型,碳库质量和脆弱程度不一。从维持地力和环境健康的角度,应对不同母质发育的土壤制定不同的开发利用方案。     

Human Influence and Classical Biogeographic Predictors of Rare Species Occurrence

Biogeographic theory predicts that rare species occur more often in larger, less‐isolated habitat patches and suggests that patch size and connectivity are positive predictors of patch quality for conservation. However, in areas substantially modified by humans, rare species may be relegated to the most isolated patches. We used data from plant surveys of 81 meadow patches in the Georgia Basin of Canada and the United States to show that presence of threatened and endangered plants was positively predicted for patches that were isolated on small islands surrounded by ocean and for patches that were isolated by surrounding forest. Neither patch size nor connectivity were positive predictors of rare species occurrence. Thus, in our study area, human influence, presumably due to disturbance or introduction of competitive non‐native species, appears to have overwhelmed classical predictors of rare species distribution, such that greater patch isolation appeared to favor presence of rare species. We suggest conservation planners consider the potential advantages of protecting geographically isolated patches in human‐modified landscapes because such patches may represent the only habitats in which rare species are likely to persist. Influencia Humana y Predictores Biogeográficos Clásicos de la Ocurrencia de Especies Raras     

Hunting Effects on Favourable Conservation Status of Highly Inbred Swedish Wolves

The wolf (Canis lupus) is classified as endangered in Sweden by the Swedish Species Information Centre, which is the official authority for threat classification. The present population, which was founded in the early 1980s, descends from 5 individuals. It is isolated and highly inbred, and on average individuals are more related than siblings. Hunts have been used by Swedish authorities during 2010 and 2011 to reduce the population size to its upper tolerable level of 210 wolves. European Union (EU) biodiversity legislation requires all member states to promote a concept called “favourable conservation status” (FCS) for a series of species including the wolf. Swedish national policy stipulates maintenance of viable populations with sufficient levels of genetic variation of all naturally occurring species. Hunting to reduce wolf numbers in Sweden is currently not in line with national and EU policy agreements and will make genetically based FCS criteria less achievable for this species. We suggest that to reach FCS for the wolf in Sweden the following criteria need to be met: (1) a well‐connected, large, subdivided wolf population over Scandinavia, Finland, and the Russian Karelia‐Kola region should be reestablished, (2) genetically effective size (N_e) of this population is in the minimum range of N_e = 500–1000, (3) Sweden harbors a part of this total population that substantially contributes to the total N_e and that is large enough to not be classified as threatened genetically or according to IUCN criteria, and (4) average inbreeding levels in the Swedish population are <0.1. Efectos de la Cacería sobre el Estatus de Conservación Favorable de Lobos Suecos con Endogamia Alta     

论DNA分子标记在家畜遗传多样性保护中的应用

本文就ＤＮＡ分子遗传标记在家畜遗传多样性保护中应用的可行性及途径进行了探讨，提出了家畜遗传多样性标记辅助保护新策略。     

基于遗传-支持向量机和遗传-径向基神经网络的有机物正辛醇-水分配系数QSPR研究

基于遗传算法(GA)的因子筛选和支持向量机(SVM)的非线性回归,提出了1种改进的有机物定量结构-性质相关(QSPR)建模方法--遗传-支持向量机(GA-SVM),并将其用于38种食品工业常用有机物正辛醇-水分配系数(Kow)的QSPR建模.结果显示,QSPR模型选取了分子量、Hansen极性、沸点、含氧率和含氢率5种参数;模型的预测值与实测值间的误差平方和(SSE)、均方差(RMSE)和决定系数(R2)分别为0.048、0,036和0.999,表明模型具有较强的预测能力;同时,交叉验证的结果(SSE=0.295,RMSE=0.089,R2=0.995)也表明,模型具有良好的稳健性,因此,GA-SVM算法适用于对有机物正辛醇-水分配系数的QSPR建模.此外,将基于GA-SVM的QSPR模型分别与基于遗传-径向基神经网络(GA-RBFNN)和基于线性算法的模型进行了比较,结果表明,应用GA-SVM建立的QSPR模型无论从稳健性还是预测能力上都优于应用其它2种算法建立的模型,因此,GA-SVM算法比GA-RBFNN和线性算法更适合于对有机物正辛醇-水分配系数进行QSPR建模.     

中国遗传资源优先保护等级评价标准的构建

确定科学合理的生物遗传资源优先保护等级,是当前保护生物学研究的一个核心问题。文章通过分析国内外遗传资源优先保护等级评价研究进展,针对遗传资源的特点,对遗传资源与物种关系、遗传资源多样性、境外种群影响、遗传资源价值、潜在利用价值、人工繁育技术、特有情况等方面进行了探讨并提出相应建议,初步确定了遗传资源优先保护等级的评价标准,以期能为生物遗传资源的有效保护和科学管理提供参考依据。     

微生物处理技术在有机污染物降解中的应用

微生物处理有机污染物是一种费用低,效果好,无二次污染且操作简单的处理方法。综述了国内外几种微生物处理有机污染物技术的研究进展。     

A comparison of different lysis buffers to assess allele dropout from single cells for preimplantation genetic diagnosis

Single cell polymerase chain reaction (PCR) for preimplantation genetic diagnosis (PGD) requires high efficiency and accuracy. Allele dropout (ADO), the random amplification failure of one of the two parental alleles, remains the most significant problem in PCR-based PGD testing since it can result in serious misdiagnosis for compound heterozygous or autosomal dominant conditions. A number of different strategies (including the use of lysis buffers to break down the cell and make the DNA accessible) have been employed to combat ADO with varying degrees of success, yet there is still no consensus among PGD centres over which lysis buffer should be used (ESHRE PGD Consortium, 1999 ). To address this issue, PCR amplification of three genes (CFTR, LAMA3 and PKP1) at different chromosomal loci was investigated. Single lymphocytes from individuals heterozygous for mutations within each of the three genes were collected and lysed in either alkaline lysis buffer (ALB) or proteinase K/SDS lysis buffer (PK). PCR amplification efficiencies were comparable between alkaline lysis and proteinase K lysis for PCR products spanning each of the three mutated loci (ΔF508 in CFTR 90% vs 88%; R650X in LAMA3 82% vs 78%; and Y71X in PKP1 91% vs 87%). While there was no appreciable difference between ADO rates between the two lysis buffers for the LAMA3 PCR product (25% vs 26%), there were significant differences in ADO rates between ALB and PK for the CFTR PCR product (0% vs 23%) and the PKP1 PCR product (8% vs 56%). Based on these results, we are currently using ALB in preference to PK/SDS buffer for the lysis of cells in clinical PGD. Copyright © 2001 John Wiley & Sons, Ltd.     

Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers

Fragile X syndrome is the most common cause of familial mental retardation. The most common mutation is expansion of a triplet (CGG)_n repeat in the 5′ untranslated region of the FMR1 gene on Xq27.3. The expansion is refractory to PCR due to preferential amplification of the smaller allele in heterozygous cells and the high GC content of the repeat and surrounding sequences. Direct detection of the normal parental alleles in preimplantation embryos has been used for preimplantation genetic diagnosis (PGD) of this disorder. However, this approach is only suitable for approximately 63% of couples due to the heterozygosity of the repeat in the normal population. As an alternative we investigated the use of polymorphic markers flanking the mutation to track the normal and premutation carrying maternal chromosomes in preimplantation embryos. Using a panel of 11 polymorphisms, six (CA)_n repeats and five single nucleotide polymorphisms, diagnosis was developed for 90% of referred couples. Multiplex amplification of informative markers was tested in 300 single buccal cells from interested couples with efficiency and allele drop out (ADO) rates ranging from 69% to 96% and 6% to 18%, respectively. Use of this approach is accurate and applicable to a larger number of patients at risk of transmitting fragile X to their offspring. Copyright © 2001 John Wiley & Sons, Ltd.     

Fetal renal anomalies and genetic syndromes

Renal abnormalities are some of the commonest and most easily detectable anomalies on ultrasound. Many are an isolated finding but the prognosis may be altered considerably by the detection of other anomalies which could indicate a genetic disorder or syndrome. It is often easier to detect presupposed anomalies and the purpose of this article is to introduce and discuss those syndromes that may present with a renal abnormality on ultrasound. Common renal findings are presented with the range of additional anomalies that should be sought and suggested diagnostic tests. It should be remembered that although for many genetic conditions specific mutation analysis is now available, this usually requires pre‒pregnancy investigations. Furthermore, in some cases the definitive diagnosis may not be suspected until post mortem. By this time it may be too late to establish a cell line to confirm the suspicion using laboratory methods. It is therefore important to take tissue samples antenatally where possible, or at delivery, as postnatal samples may have a high culture failure rate. Copyright © 2001 John Wiley & Sons, Ltd.