放牧和模拟降水对短花针茅荒漠草原植物功能群多样性的影响

为探究放牧和降水变化对植物功能群的影响,本文以内蒙古短花针茅(Stipa breviflora)荒漠草原为研究对象,开展了野外控制试验。试验设置围封和适度放牧,分别进行模拟降水处理(减少降水量50%、自然降水、增加降水量50%、增加降水量100%),并在每年8月观测植物群落组成。结果表明：减水会降低植物功能群多样性、生物量和物种数量,增水有利于植物功能群多样性的提高。多年生丛生禾草多样性随降水量的增加而升高。同时,对降水梯度和功能群多样性进行拟合分析发现,降水量低于年降水量16%则不利于除灌木、半灌木外其他功能群植物的生长。围封草地增水67%～79%时,功能群的Simpson指数、Shannon-Wiener指数、Pielou指数值均较高,功能群多样性较高;由于放牧提高了植物的水分利用效率,放牧地各指数在增水26%～50%时较高,功能群多样性较高。综上,适度的放牧及水分补充有利于提高植物功能群多样性。     

生物多样性与地形及土壤因素对坡面产流产沙的耦合影响

生物多样性关系到生态系统的功能,而坡度和土壤因素是影响坡面产流产沙的重要因子。本研究基于黄土丘陵区生物多样性,并引入坡度、降雨前土壤含水量和土壤容重,探究其与坡面产流产沙总量的耦合关系。通过野外人工降雨试验,记录草本、灌木和乔木群落下的产流时间和产流产沙总量,并开展土壤植被调查。结果表明,与草本和乔木群落相比,灌木群落在延长产流开始时间和降低产沙总量上表现更优;植被群落功能离散度指数(FDiv)对产沙总量影响最大,Simpson指数(D)对产流总量影响最大,坡度仍然是不可忽视的第二重要影响因素;产流总量与坡度、土壤容重、D和功能丰富度指数(FRic)的回归关系优于产流总量分别与其的回归关系;产沙总量与坡度和FDiv指数的回归关系优于产沙总量分别与其的回归关系。植被保护与坡度改善将是该区水土保持规划工作的重点。     

刈割强度对大针茅草原植物群落特征和土壤理化性质的影响

探究不同刈割强度对大针茅典型草原植物群落特征以及土壤理化性质的影响,可为大针茅草原制定合理科学的刈割制度提供理论依据。本研究以大针茅典型草原为对象,于2020年在内蒙古锡林浩特市毛登牧场刈割实验平台进行野外植被调查和取样。该实验平台于2014年建立,以不刈割为对照（CK）,设置轻度（LM）、中度（MM）及重度刈割（HM）3个处理。本研究通过计算物种重要值和多样性指数,测定植物群落地上、地下生物量以及土壤理化性质,探究群落特征与土壤理化性质的关系。结果表明：1）与不刈割相比,不同刈割强度均增加了新物种,且中度刈割的物种数最多;与不刈割相比,不同刈割强度均显著增加了群落的丰富度和Shannon-Wiener指数,且轻度刈割显著增加了优势度和均匀度指数,表明轻度刈割最有利于群落多样性的维持;不同刈割强度对大针茅草原的生产力均无显著影响;2）土壤全碳、全氮和pH均在中度刈割时最高,且显著高于不刈割,表明中度刈割对土壤养分有积极影响;3）硝态氮是影响草地生产力的主要土壤因子,土壤含水量是影响草地群落多样性的主要土壤因子。本研究可为大针茅典型草原群落结构、物种多样性以及生产力等方面的研究提供重要参...     

A Spot Price Model with Var Cost

This paper has applied the var cost to the theory of spot price.An augmented Lagrange method is employed to develop the exact model of spot price of active power and reactive power,and the physical means of Lagrange multipliers are explained.The numerical examples are given to demonstrate the validity of the proposed model.     

Study on Genetic Fingerprinting Technique of Microbial Communities

The 99% of all microorganisms in naturecannot be isolated by standard culture methods without conspicuous external characters to classify them morphologically. In addition, classification based on physiological or biochemical features are often fuzzy. Molecular techniques are used for uncultured microorganisms to explore the diversity of microbial communities and novel resources without the need of cultivation. DNA dynamics and cloning of PCR products obtained from environmental DNA is now routinely used to identify microbial populations in microbial ecology. For practical reasons the approach is not suited to study the complex dynamics of microbial communities in environment. Genetic fingerprinting techniques are better tools, which give complement for the traditional microbiological methods. The methods are rapid and relatively easy to perform, and they allow the simultaneous analysis of multiple samples, which makes it possible to compare the genetic diversity of microbial communities from different habitats, or to study the behaviour of individual communities over time.     

Determination of vc and mating types of Cryphonectria parasitica isolates by multiplex PCR and their genetic diversity in 13 chestnut-growing provinces of Turkey

Vegetative compatibility (vc) and mating types and genetic diversity of Cryphonectria parasitica isolates were determined using 183 isolates obtained from 215 infected chestnut trees growing in 13 provinces of Turkey. Based on the cultural aspects, 143 of these isolates were evaluated as virulent whereas the remaining 40 isolates were hypovirulent. When vc types of 183 isolates were classically differentiated, 135 of them matched to EU-1 (82.3%), 29 of them to EU-12 (17.6%) vc type, whereas 19 of them did not match to the two. When molecular vic markers were used, all the isolates were assigned to two EU vc types; 149 to EU-1 (81.4%) and 34 (18.5%) to EU-12. Of the majority of the isolates, 134 (73.2%) had mating-type MAT-1, while 44 (24%) isolates had MAT-2 and 5 (2.8%) isolates had both mating types. The population analysis based on two DNA marker systems, Inter-Primer Binding Site and Start Codon Targeted Polymorphism, showed no intraspecific genetic variation among the C. parasitica isolates. The prevalence of two dominant vc types revealed by this study shows that biological control with hypovirulent EU-1 and EU-12 isolates will be significant for the country. The results might be helpful to chestnut breeders carrying out resistance breeding studies to manage this disease based on hypovirulence attributed to Cryphonectria hypovirus 1.     

基于表型和基因型的藜麦种质资源遗传多样性分析

为了解和掌握青海省引进和收集藜麦种质资源的遗传背景和多样性,本研究选择11个表型性状和221对SSR引物对114份藜麦种质资源进行遗传多样性分析。结果表明,114份藜麦种质资源的11个表型性状差异极显著（P＜0.01）,变异系数范围为4.57%~87.79%,主穗直径的变异最大（87.79%）,籽粒直径的变异最小（4.57%）;遗传多样性指数范围为0.47~2.29,单株产量的遗传多样性指数最大（2.29）,茎秆长最小（0.47）。46对多态性较好的SSR引物扩增出165条多态性条带,每对引物的平均等位变异数为3.59,观测等位基因（Na）平均值为1.65,有效等位基因（Ne）平均值为1.50,Shannon’s信息指数（I）和Nei’s基因多样性指数（He）平均值分别为0.39和0.27,平均多态性比率为64.35%。通过聚类分析发现,114份藜麦种质基于表型性状和SSR分子标记的聚类结果存在一定的相似和差异,来源地相同的种质被分到了不同的类群,来源地不同的种质被分到了同一类或单独聚成一类,说明参试藜麦种质资源的表型性状和分子遗传信息多样性较丰富。     

不同栽培类型蓝莓遗传多样性的SSR分析

以南方地区的蓝莓品种为主要对象,利用SSR标记分析现有品种种质的遗传多样性。设计合成了56对蓝莓SSR分子标记引物,进行扩增和多态性引物筛选,将多态性好的引物用于66份蓝莓不同类型种质的遗传多样性分析。结果表明,56对引物均能扩增出预期大小条带,其中条带清晰多态性较好的引物为25对,占比引物数的44.64%,多数引物扩增的位点数在5~7个之间。25对引物在66份蓝莓供试种质中检测多态性,共检测到165个等位变异,平均每个位点有6.6个等位变异,PIC值变幅为0.656~0.947,平均值为0.777。多态性最好的引物Vc26可以检测到15个等位基因数目。北方高丛、南方高丛和兔眼类型66份蓝莓种质的遗传相似系数位于0.60~0.96之间,品种间遗传差异较丰富。利用UPGMA聚类将3种类型种质进行分析,发现除了兔眼类型品种‘红粉佳人’外,其余明显分为3个类群,且同一类型的种质基本聚在一起。结合不同类型种质的系谱分析,发现分类与品种种质的遗传成分相似有一定的相关。研究利用SSR分子标记揭示了蓝莓不同类型种质的遗传多样性,对今后杂交育种亲本选择利用有一定借鉴意义。     

贵州野生枇杷资源遗传多样性的ISSR分析

本文采用ISSR标记,构建了贵州39份野生枇杷种质的DNA指纹图谱,并对其遗传多样性进行了评价。结果表明,以筛选出的15条引物进行PCR扩增,获得清晰、重复性好的谱带125条,其中多态性谱带108条,多态性比例为86.4%;应用引物815、825和841的组合,构建了39份枇杷种质的ISSR指纹图谱,可以有效区分所有供试材料;15条引物的谱带数据聚类分析表明,供试种质的遗传相似性系数为0.40~0.98,在相似性系数为0.70时,可将供试种质分成五大类。聚类结果与种质表型相关,与地理分布的相关性不明显。     

贵州荞麦重要种质的遗传多样性分析及分子身份证构建

为精准鉴定贵州荞麦种质资源,采用SSR分子标记对60份荞麦种质进行遗传多样性分析,构建DNA分子身份证数据库。结果显示,从100对SSR引物中筛选出16对稳定性好、多态性丰富的引物,在60份供试种质中共扩增出174个多态性条带;Shannon’s信息指数、Nei’s多样性指数、多态信息指数均值分别为0.337、0.206、0.693,引物的多态性较好,能有效揭示60份荞麦种质的遗传多样性;在Dice遗传相似系数为0.374时,所有供试材料可聚为A、B、C 三组;当Dice遗传相似系数为0.484时,将苦荞组（A组）更细分为A1、A2两个小组。采用毛细管电泳及8%的聚丙烯酰胺凝胶（PAGE）电泳对SSR标记扩增产物进行双验证,2种方法的聚类结果一致。结果表明,本研究开发的高效性SSR分子标记能够有效地鉴定贵州荞麦重要种质的遗传多样性且用于构建分子身份证。