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1.
本文记述了中国鳞(虫兆)属1新种:王朗鳞姚Tommocerus(Tomocerina)wanglangensis,sp.nov.。模式标本保存于西南科技大学生命科学与工程学院昆虫标本室。王朗鳞虫兆Tomocerus(Tomocerina)wanglangensis,新种(图1~9)本新种和白鳞姚T.(Tomocerina)calceus Liu et al.1999非常相似,但新种爪内缘齿为1,1,1;弹器齿节刺简单、不具褶,刺序为2/1,Ⅰ,1,Ⅰ;弹器端节间齿数为2。正模♀,四川省平武县王朗,1800m,06-X-2002,刘永琴;副模:3♀♀,5♂♂,同正模。  相似文献   

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中国鳞虫兆属Tom ocerus四新种(弹尾目:鳞虫兆科)   总被引:9,自引:2,他引:7  
本文记述了中国鳞虫兆属Tom ocerus4新种,即紫胸鳞虫兆Tom ocerus(Tom ocerina) pur-purithorus, sp. nov., (四川); 白鳞虫兆Tomocerus(Tom ocerina) calceus, sp. nov., (四川);巨鳞虫兆Tomocerus(s.str.)m aximus,sp.nov.(四川);小鳞虫兆Tom ocerus(s.str.)em eicus, sp. nov. (四川)。模式标本保存于绵阳经济技术高等专科学校农艺系昆虫标本室。1. 紫胸鳞虫兆Tom ocerus(Tomocerina) purpurithorus, 新种(图1)鉴别特征:本种与T.(Tom ocerina) m inutusTullberg 1876 非常相似,但其下列特征可与后者相区别:弹器齿节刺的刺式为5/7,1,弹器端节间齿数为5~7,爪内齿数为1,1,1,握弹器体上刚毛数为5支。正模:♀,四川峨眉山,19- IV- 1995,刘永琴;副模:4♀♀2♂♂,同正模。2. 白鳞虫兆Tom ocerus (Tom ocerina) calceus, 新种(图2)鉴别特征:本种与T.(Tomoceri  相似文献   

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报道中国鳞(虫兆)属(弹尾纲,鳞(虫兆)科)1新纪录种,即刻点鳞(虫兆)Tomocerus punctam Yosii,1967,并对其进行重新描述.该种已知分布于日本,齿节刺简单,仅最后1个2分叉.观察标本保存于中国科学院动物研究所.  相似文献   

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本文记述了中国鳞属1新种:王朗鳞Tomocerus(Tomocerina)wanglangensis,sp.nov.。模式标本保存于西南科技大学生命科学与工程学院昆虫标本室。王朗鳞虫兆Tomocerus(Tomocerina)wanglangensis,新种(图1~9)本新种和白鳞虫兆T.(Tomocerina)calceusLiuetal.1999非常相似,但新种爪内缘齿为1,1,1;弹器齿节刺简单、不具褶,刺序为2/1,Ⅰ,1,Ⅰ;弹器端节间齿数为2。正模♀,四川省平武县王朗,1800m,06-Ⅹ-2002,刘永琴;副模:3♀♀,5♂♂,同正模。  相似文献   

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记述浙江省洞头岛拟祼长角虫兆属1无眼新种,岛屿拟裸长角虫兆Coecobrya islandica Shi&Pan sp.nov.。此新种的鉴定特征为无眼,弹器基具"光滑"刚毛,胫胕节内侧无"光滑"刚毛,下唇MREL1L2为光滑刚毛,X和X4为光滑刺状小刚毛,上唇基刚毛,腹部第II–IV节的感觉毛以及背部毛序。该新种与短毛拟裸长角虫兆Coecobrya brevis Xu et al.,2012最相似。本文给出了该新种的特征图及与相似种的详细特征比较。模式标本保存于台州学院生命科学学院和南京农业大学植保学院昆虫系。  相似文献   

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记述浙江省大雷山刺齿虫兆属 1 新种,张氏刺齿虫兆Homidia zhangi sp. nov., 该种鉴别特征有体色,光滑下唇毛 L1,腹部第 4 节后侧中间 3+3 根大刚毛及长度相近的特化毛,腹部第 1 节和第 5 节特化毛的相对位置以及腹管侧瓣和弹器端区的大量纤毛状刚毛。模式标本保存于南京大学生命科学学院和台州学院生命科学学院。  相似文献   

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本文记述了鳞属华东地区1新种——近似鳞Tomocerus(s.s.)similis,sp.nov.。本新种和克洛鳞T.(s.s.)kinoshitaiYosi,1954非常相似,但可从小爪内齿、头部毛序及弹器齿节上棘状刚毛等特征相区别。正模♀,江苏滁县琅琊山,1990-IV-8,8040;副模:1♀,同正模;安徽黄山:1♂,2♀♀,1990-VI-3,8164、8169和8172;2♀♀,1990-VI-16,8222;1♀,1993-IX-12,8344;江苏:1♂,句容县宝华山,1990-V-28,8125;1♀,南京紫金山,1994-IV-9,8355;1♀,灌云县,1995-I,8437。模式标本保存于南京大学生物系。  相似文献   

8.
记述弹尾目Collembola鳞[虫兆]科Tomoceridae鳞[虫兆]属Tomocerus1新种,即斑点鳞[虫兆]Tomocerus(Tomocerus)maculatus sp.nov.和1新纪录种,即巴地鳞Tomocerus(Tomocerus)asoka Yosii et Ashraf,1965。新种模式标本保存于中国科学院动物研究所。 斑点鳞[虫兆],新种Tomocerus(Tomocerus)maculatus sp.nov.(图1 ~10 ,表1) 体长2.3 ~3.1mm。 正模♀,吉林长白山(42.0°N,128.1°E) ,1100m,1980-08-03 ,黄复生采(IZCAS)。副模1 ♂,记录同正模; 1♀,吉林二道白河(42.4°N, 128.1°E),700m, 1981-08-04 ,黄复生采(IZCAS)。 新种与T.(T.)violaceus Yosii,1956相似,但齿刺基部排列方式,触角、头部和身体上色素分布等不同。 词源:种名意指腹部3,4,5节上的斑块。  相似文献   

9.
西藏鳞(虫兆)亚属二新种记述(弹尾目,鳞(虫兆)科)   总被引:1,自引:1,他引:0  
记述采自西藏地区的弹尾目Collembola鳞(虫兆)科Tomoceridae鳞(虫兆)亚属Tomocerus(Tomocerus)2新种:黑带鳞(虫兆)Tomocerus(Tomocerus)nigrofasciatus sp.nov.(西藏:洛扎生格)和背崩鳞(虫兆)Tomocerus(Tomocerus)baibungensis sp.nov.(西藏:墨脱背崩),给出鉴别特征图以及在西藏地区的种检索表.新种模式标本保存在中国科学院动物研究所.  相似文献   

10.
记述采自山西地区的弹尾目Collembola鳞(虫兆)科Tomoceridae鳞(虫兆)属Tomocerus 2新种:黑鳞(虫兆)Tomocerus(Tomocerus)nigrus sp.nov.(山西:和顺禅堂寺)和霍县鳞(虫兆)Tomocerus(Tomocerus)huoensis sp.nov.(山西:霍县七里峪侧尾).新种模式标本保存在中国科学院动物研究所.  相似文献   

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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.  相似文献   

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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.  相似文献   

17.
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.  相似文献   

18.
肝癌中HBV和HCV基因和抗原的分布及意义   总被引:1,自引:0,他引:1  
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  相似文献   

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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.  相似文献   

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