松嫩平原南部主要群落植物多样性的比较研究

应用Ｍａｒｇａｌｅｆ（Ｒ１）和Ｍｅｎｈｉｎｉｃｋ（Ｒ２）丰富度指数、Ｈｉｌｌ多样性指数（Ｎ１,Ｎ２）和Ｐｉｅｌｏｕ均匀度指数（Ｅ）比较研究了松嫩平原南部１４个主要群落的植物多样性、生活型多样性及植物多样性与群落演替的关系结果表明,分布于低平原的羊草－蔓萎陵菜群落的植物多样性和丰富度指数最大,Ｒ１为１１．９６,Ｒ２为５．２４,Ｎ１为１３．９２,Ｎ２为８．７６,分布于固定砂丘的榆树疏林和贝加尔针茅等４个群落有较高的植物多样性,而分布于碱化草甸的角碱蓬等群落植物多样性最小,Ｒ１为１．３１,Ｒ２为０７１,Ｎ１为１．８４,Ｎ２为１．４６．具有较高植物多样性的群落其植物生活型多样性指数也较高．在演替系列中,羊草群落的植物多样性指数介于演替初期和中期阶段之间．     

昆嵛山老杨坟阳坡与阴坡半天然植被植物群落生态学特性的初步研究

本文对昆嵛山老杨坟阳坡与阴坡半天然植被植物群落的上层（乔木层）和下层（灌木层）的物种优势度、多样性指数、群落的均匀度、相似性指数以及群落的最小面积进行了分析。昆嵛山老杨坟半天然植物群落上层的最小面积应为３００ｍ２,下层应为２２５ｍ２。阳坡与阴坡植物群落的上层和下层优势种的分布格局存在一定差异;乔木层的物种多样性指数,阴坡大于阳坡,灌木层阳坡大于阴坡,但二者的差异水平不显著;两群落乔木层的均匀度指数存在显著差异。阳坡与阴坡植物群落乔木层的相似性指数低于灌木层,并且以相对盖度和相对优势度（相对重要值）为基础统计所得到的群落相似性指数更好地反映了群落间乔木层在结构和功能上的差异。     

宁夏东部风沙区荒漠草原植物群落物种多样性研究

通过野外植被调查,研究了宁夏东部风沙区荒漠草原植物群落组成与结构、物种多样性变化;采用典范对应分析（CCA）对植物群落分布与土壤性状关系进行了分析。结果表明：（1）风沙区荒漠草原物种较为单一,多集中在6~13种;不同群落类型间地上生物量和盖度差异显著;群落内竞争性较弱的物种减少,优势种具有较高的重要值。（2）群落间物种多样性差异显著,但变化趋势并不一致;物种多样性指数与丰富度指数、均匀度指数的相关系数分别为0.975 7和0.880 2,而与优势度指数相关系数为-0.519 8。（3）CCA结果表明,土壤含水率、有机质以及氮磷钾含量较高、容重小时,植物物种相对丰富;对群落分布影响较大的环境因子是土壤水分、容重和土壤有机质,相关系数分别为-0.742 8、0.683 8、0.532 9,物种和群落二者在CCA排序轴相关性较大的土壤因子较为一致。研究认为,宁夏东部风沙区荒漠草原植物优势种在群落中的地位明显,物种丰富度对植物多样性的影响大于均匀度,土壤水分是影响该区草原植物群落分布的决定性环境因子。     

安西荒漠植物群落和优势种的分布与环境的关系

应用排序（ＤＣＡ）和回归分析方法对安西砾石戈壁荒漠植物群落及优势种的分布与环境的关系进行了研究。结果表明,该区群落的盖度（Ｃ）和密度（Ｄ）均与年降水量（Ｒ）有密切关系,而群落的种类丰富度（Ｎ）则与土壤含盐量（Ｓ）相关,其回归关系式为：Ｃ＝０．０５１９６８１６３ｅ０．０４０７８６８２１Ｒ（Ｒ＝０．９５,Ｐ＜０．０１）,Ｄ＝０．２７１４７９１３ｅ０．０５２７４１８２９Ｒ（Ｒ＝０．９６,Ｐ＜０．０１）,Ｎ＝１３．７７４８－６．４７７３０３ｌｇ１０００Ｓ（Ｒ＝０．８３,Ｐ＜０．０１）。即：年降水量是决定戈壁荒漠植物群落盖度和密度的主要因素,土壤含盐量则与群落种类丰富度的关系尤为突出。优势种的抗旱性顺序是：红砂（Ｒｅａｕｍｕｒｉａｓｏｎｇｏｒｉｃａ（（Ｐａｌ．）Ｍａｘｉｍ．）＞泡泡刺（ＮｉｔｒａｒｉａｓｐｈａｅｒｏｃａｒｐａＭａｘｉｍ．）＞黑柴（ＳｙｍｐｅｇｍａｒｅｇｅｌｉＢｇｅ．）＞珍珠（ＳａｌｓｏｌａｐａｓｅｒｉｎａＢｇｅ．）＞膜果麻黄（ＥｐｈｅｄｒａｐｒｚｅｗａｌｓｋｉＳｔａｐｆ．）,而耐盐性顺序是：珍珠＞红砂＞黑柴＞泡泡刺＞膜果麻黄     

长白山阔叶红松林植物群落与昆虫群落的相互关系研究

通过季节性的观察,系统研究了长白山植物群落、昆虫群落多样性及它们之间关系。结果表明,植物群落物种丰富度指数与植食性昆虫丰富度指数呈负相关,而与捕食性天敌昆虫丰富度指数呈正相关,与寄生性天敌的丰富度指数呈负相关;昆虫群落的均匀度与植物群落的均匀度相关显著。植物群落的多样性指数与捕食性、寄生性天敌的多样性指数呈正相关。而与植食性昆虫的多样性指数呈负相关,这表明植物群落的多样性影响昆虫群落的多样性。     

塔里木荒漠河岸林异质生境物种多样性比较与其测度指标筛选及评价

选择合适的物种多样性测度指标与多样性指数是进行群落多样性研究的基础工作。依据塔里木河上游荒漠河岸林样地调查资料,分别采用重要值、盖度和多度为测度指标比较了反映群落物种丰富度、多样性、均匀度和优势度12种多样性指数与异质生境群落多样性特征,并对多样性指数进行了相关分析与评价。结果表明,荒漠河岸林异质生境群落物种组成种类差异明显,轮南镇胡杨群落物种丰富度与多样性指数最高,水工三连灰胡杨群落多样性最低,土壤水盐的空间异质性是引起荒漠植被空间分布与群落多样性差异的主导因子。表征荒漠群落多样性以重要值和盖度为测度指标优于多度指标,其中以重要值为测度指标来反映群落多样性更为合理。相关与主成分分析表明,均匀度与多样性指数间的相关性高于丰富度与多样性指数,且多样性指数受均匀度、优势度指数受丰富度影响较大,反映出荒漠河岸林群落多样性主要决定于物种分布的均匀程度。12种多样性指数中Margalef丰富度指数（Ma）、Shannon-Weiner多样性指数（H）与Simpson多样性指数（D）能客观真实地反映异质生境荒漠植物群落多样性。同时,针对高度生境异质性的荒漠植物群落,还应综合考虑群落物种组成与生境特征,选择合适的多样性指数组合可更客观地反映荒漠河岸林群落多样性变化。     

库姆塔格沙漠南缘荒漠植物群落多样性分析

 根据20个样地的调查资料,应用重要值计算多样性指数、均匀度指数、丰富度指数 、优势度指数,对库姆塔格沙漠南缘荒漠植物群落物种多样性进行分析。结果表明: 1）荒漠植物群落分布随其生境地貌不同而不同,山前戈壁上分布有合头草(Sympegma regelii)群落,冲积河道低地分布有荒漠林胡杨(Populus euphratica)、多枝柽柳(Tamarix ramosissima)、胀果甘草（Glycyrrhiza inflata）群落,戈壁沙漠过渡带为梭梭(Haloxylon ammodendron)群落,低海拔的沙山上分布有沙拐枣(Calligonum mongolicum)群落、膜果麻黄(Ephedra rzewalskii)群落和梭梭群落。2）荒漠植物群落物种多样性水平较低,群落结构简单,物种组成单一。群落Shannon_Wiener物种多样性水平表现为合头草群落最高（1.706）,具有草原化荒漠植被类型的成分;梭梭群落、膜果麻黄群落居中（0.875～0.890）,荒漠植被类型特征明显;沙拐枣群落、胡杨群落、多枝 柽柳群落、胀果甘草群落较低（0.079～0.495）,荒漠林、盐地沙生灌丛及盐化草甸植被均有零星分布。3）荒漠植物群落结构层次中,灌木层占居主导地位,群落灌木层物种多样性水平（0.769～1.451）远远大于草本层（0.193～0.254）,且草本层物种多样性受灌木层影响较大。4）荒漠植物群落物种多样性分布格局表现为经向、纬向和海拔梯度的变化,经向、纬向变化为物种多样性水平较高的草原化植物合头草群落（1.706）向物种多样性水平较低的荒漠植物梭梭群落（1.379）和盐化植物多枝柽柳群落（0.376）的过渡,海拔梯度则 呈现低水平的沙拐枣群落（0.819）到高水平的膜果麻黄群落（0.890）向低水平的梭梭群落 （0.645）变化。荒漠植物群落过渡地带一般具有较高的物种多样性和较低的生态优势度。     

黄河三角洲自然保护区典型植物群落物种组成及多样性梯度变化

以黄河三角洲自然保护区典型湿地群落为研究对象,探讨其物种组成及物种多样性的梯度变化规律。结果表明,从芦苇－香蒲群落到翅碱蓬群落梯度上：（1）群落物种丰富度呈波动性变化,旱柳－芦苇－白茅群落的物种丰富度最高,其次是芦苇－柽柳－翅碱蓬群落、芦苇－香蒲群落、柽柳－翅碱蓬群落,翅碱蓬群落的物种丰富最低;（2）群落的α多样性的变化格局与丰富度的变化格局不太一致,其中Shannon-Winner多样性指数与Pelou均匀度指数表现为波动性的下降趋势,而Simpson优势度指数则表现为波动性的上升趋势;（3）群落的β多样性变化格局也不完全相同,其中相异性系数呈波动性降低趋势,Copy指数则表现为先升高再降低的变化趋势。黄河三角洲典型湿地植物群落组成和物种多样性的梯度变化主要与生境变化有关。     

黑龙江丰林自然保护区大型真菌群落多样性研究

对黑龙江省丰林自然保护区大型真菌的群落多样性进行了研究。共设置类型Ⅰ（红松纯林）、类型Ⅱ（云、冷杉红松林）、类型Ⅲ（椴树红松林）、类型Ⅳ（蒙古栎红松林）、类型Ⅴ（枫桦红松林）5种类型的植物群落,对群落内的大型真菌种类和数量进行了调查。采用Menhinick物种丰富度指数（R）、Shannon—wiener多样性指数（H...     

佛坪国家级自然保护区植物群落物种多样性特征

用物种多样性指数（Simpson指数和Shannon指数）、均匀度指数（Pielou均匀度）和物种丰富度,对佛坪国家级自然保护区主要高等植物群落物种多样性进行了测度。结果表明：森林群落的多样性程度高于灌丛和草甸,落叶阔叶林高于针叶林,栎林高于杨桦林。群落物种多样性有随海拔高度的升高而降低的趋势。物种多样性在森林群落垂直结构上的分布特点,表现为一般乔木层与灌木层接近但低于草本层。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

The structure, reproduction and taxonomy of Vidalia and Osmundaria (Rhodophyta, Rhodomelaceae)

Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.     

New or rare chromosome counts in Artemisia L. (Asteraceae, Anthemideae) and related genera from Kazakhstan

Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.     

肝癌中HBV和HCV基因和抗原的分布及意义

采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细     

Selection with two alleles and complete dominance

For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.