河南新(虫责)属(襀翅目,(虫责)科)一新种记述

记述采自河南的1新种,河南新Neoperla henana sp.nov.,并讨论了其与近似种的区别。模式标本保存在河南科技学院标本馆。河南新,新种Neoperla henana sp.nov.(图1～5)新种腹部第7背板隆突和第8背板的骨化突特征与师周新Neoperla magisterchoui Du,2000近似。二者的主要区别在于:新种雄虫阳茎囊略长于阳茎管,阳茎管端部有1对膜质突起。而师周新雄虫阳茎囊长度约为阳茎管的两倍,阳茎管端部有两对膜质突起。正模♂,河南南阳老界岭,2008-07-02,李卫海采,副模1♂,同正模。词源:新种以标本的模式产地命名。     

贵州钩(虫责)属一新种记述((襀)翅目:(虫责)科)

记述采自贵州宽阔水保护区的钩(虫责)属l新种:巨刺钩(虫责)Kamimuria grandispinata Du ＆Sun,sp.nov.,该新种的阳茎特征与长刺钩虫责K.longispina Wu相似,但长刺钩(虫责)阳茎囊背面近端部有1膜质突起,上面生有粒状微刺,而新种阳茎囊背面近端部是1个近似三角形的刺斑,无突起...     

中国陕西诺(虫责)种团(襀翅目,卷(虫责)科)一新种记述

记述宁夏卷1新种,即龙潭诺Rhopalopsole longtana sp.nov.,并讨论了其与近似种的区别。模式标本保存在中国农业大学博物馆。龙潭诺,新种Rhopalopsole longtana sp.nov.(图1～8)新种与秦岭诺R.qinlinga Sivec&Harper,2008近似,肛侧突大型,具强骨化的刺突,同属于陕西诺种团。二者的主要区别在于:新种雄虫第9背板后缘中部有1隆起的横脊和三角形刺突,其两侧各有1个向后延伸的叶状突,肛上突端部三角形。而秦岭诺雄虫第9背板无刺突,后缘略平直,肛上突端部圆钝。正模♂,宁夏泾源龙潭,2008-07-05,刘经贤采。词源:新种种名以采集人的姓氏命名。     

中国短菌蚊属四新种记述(双翅目,菌蚊科)

记述中国短菌蚊属4新种,模式标本保存在浙江林学院昆虫标本室.丛毛短菌蚊,新种Brevicornu caespitose sp.nov.(图1～3)雄翅长2.7～2.9 mm.新种与分布于蒙古的B.bipar-titum Lastovka et Matile,1974相似,但后者的生殖基节后缘无特殊构造,尾须和生殖刺突构造也明显不同.正模♂,浙江德清莫干山,1992-04-18,吴鸿采;副模1♂,同正模.雅致短菌蚊,新种Brevicornu concinnuse sp.nov.(图4～5)雄翅长4.5 mm.新种与广布于欧洲的B.proximum(Staeger,1840)相近似,但后者的尾须和生殖基节后缘的构造不同.正模♂,湖北武当山,1984-06-01,杨集昆采.冠状短菌蚊,新种Brevicornu coronanse sp.nov.(图6～8)雄翅长2.2～2.4 mm.新种与分布于欧洲的B.grise-icolle(Stacger,1840)相近似,但后者的毛序略不同,尾须的构造明显有差异.正模♂,陕西佛坪三官庙,1996-07-03,邢连喜采;副模1♂,甘肃迭部腊子口,1980-08-12,杨集昆采.狭椭短菌蚊,新种Brevicornu lanceolatum sp.nov.(图9～11)雄翅长2.7 mm.新种与分布于我国四川的B.chi-nense Zaitzev,1988相似,但后者的生殖刺腹突细长.正模♂,浙江庆元百山祖,1993-10-25,吴鸿采.     

中国根瘿蚊属新纪录及两新种记述(双翅目,瘿蚊科)

对根瘿蚊属Rhizomyia Kieffer的属征进行修订,并记述采自云南、贵州、海南和福建的该属两新种,分别命名为细叉根瘿蚊Rhizomyia leptodicrata sp.nov.和新月根瘿蚊Rhizomyia meniscata sp.nov..模式标本保存于南开大学昆虫标本馆.细叉根瘿蚊,新种R阮脚驴h卸todicrata sp.nov.(图1～5,9～13)新种与分布于俄罗斯的俄根瘿蚊R.rossica Mamaev&Zaitzev和塔根瘿蚊兄turr~ormis Fedotova&Sidorenko以及分布中国的新月根瘿蚊Rhiwmyiz meniscata sp.nov.在雄性成虫阳茎上的特征相似,但区别明显:新种雄性成虫阳茎端部具两个细长的尖锐突起,而R.觚豇∞雄性成虫阳茎端部具两个圆突,R.turnformis雄性成虫阳茎端部具两个分叉状的突起,R.meniscata雄性成虫阳茎端部具两个角状尖突.正模♂,云南普洱(思茅)菜阳河保护区(22.48°N,100.58°E;海拔1500m),2002-05-17,卜文俊马氏网捕.副模:1♂,同正模;4♂ ♂,云南普洱(思茅)菜阳河保护区倮倮新寨山(22.48°N,100.58°E),2002-05-23,其它同正模.词源:新种种名leptodicrata为一阴性复合拉丁形容词,意为“细长分叉的”,指该种雄性成虫阳茎端部呈细长分叉状.新月根瘿蚊,新种R阮z埘秒谊meniscata sp.nov.(图6～8,14 ～18)新种与近似种区别如上.正模♂,贵州梵净山(27.5°N,108.4°E;海拔1 350 m),2002-05-29,王新谱马氏网捕.副模:1 ♂,海南坝王岭(19°N,109°E;海拔900 m),1988-05-10,卜文俊灯诱;1♂,福建武夷山桐木七里桥(27.7°N,117.6°E;海拔1000 m),1993-04-30,卜文俊捕.词源:新种种名meniscata为一阴性拉丁形容词,意为“新月形的”,指该种雄性成虫阳茎端部背腹向呈新月形.     

中国星水虻属五新种(双翅目,水虻科)(英文)

记述我国星水虻属5新种,即基褐星水虻Actina basalis sp.nov.,贡山星水虻A.gongshana sp.nov.,长角星水虻A.longa sp.nov.,腾冲星水虻A.tengchongana sp.nov.和张氏星水虻A.zhangae sp.nov.。新种模式标本保存在中国农业大学昆虫博物馆。1基褐星水虻,新种Actina basalis sp.nov.(图3～4)新种与西藏星水虻A.xizangensis Yanget Nagatomi有些近似,但触角比头部短,中足胫节基部暗黄色。正模♂,云南金平保护站,2006-05-18,张俊华采。副模2♂♂,云南金平丫口,2006-05-18,张俊华采。2贡山星水虻,新种Actina gongshana sp.nov.(图5～6)新种与双叶星水虻A.bilobata Li,Zhanget Yang近似,但前足胫节褐色且基部暗黄色,触角鞭节黑色且基部黄褐色,阳茎三叶。正模♂,云南贡山丹侏,2007-05-18,刘星月采。副模2♂♂,同正模。3长角星水虻,新种Actinalonga sp.nov.(图1～2)新种与变星水虻A.varipes Lindner近似,但头胸背面紫色,触角比头部长。正模♂,西藏林芝,3050m,1978-06-04,李法圣采。4腾冲星水虻,新种Actina tengchongana sp.nov.(图7～8)新种与黄端星水虻A.apici flava Li,Zhanget Yang近似,但头部背面紫色,生殖基节腹面愈合部基部呈V型凹缺,阳茎中叶钝而侧叶端部稍内弯。正模♂,云南腾冲自治,2007-05-31,刘星月采。5张氏星水虻,新种Actinazhangae sp.nov.(图9～10)新种与长突星水虻A.elongata Li,Zhanget Yang很近似,但后足腿节无褐色前条纹,后足胫节基部褐色,M3不直接与盘室相连。正模♂,云南金平丫口,2006-05-18,张俊华采。     

中国细突野螟属分类学研究及三新种描述(鳞翅目,野螟亚科)

记述中国细突野螟属Ecpyrrhorrhoe Hübner 3新种,包括弯细突野螟E.aduncis sp.nov.,刺细突野螟E.multispinalis sp.nov.和狭瓣细突野螟E.angustivalvaris sp.nov..文中提供了每个种的成虫和外生殖器特征图,以及本属所有中国已知种的分种检索表和分布图.弯细突野螟,新种Ecpyrrhorrhoe aduncis sp.nov.(图1,5,8)本种外形与指状细突野螟E d~italiforrnis Zhang,Li etWang,2004近似,但雄性外生殖器抱器瓣近等宽,抱器下突弯钩状,阳茎基环侧臂末端无齿,阳茎端膜有1粗大的刺,无角状器;雌性外生殖器小囊突Z形.指状细突野螟E魄锄蜘删矗之雄性外生殖器抱器瓣端部渐窄,抱器下突指状,阳茎基环侧臂近末端有齿,阳茎端膜有1束弯刺和1排小刺,有角状器;雌性外生殖器小囊突V形.正模♂,台湾台北四崁水,海拔550 ～ 600m,2006-08-04,李后魂、杜喜翠采,外生殖器玻片号GQ11127.副模1♀,采集记录同正模(外生殖器玻片号GQ11131♀).分布:中国(台湾).刺细突野螟,新种Ecpyrrhorrhoe multispinalis sp.nov.(图2～3,6,9)本种外形与红纹细突野螟E rub~inalis Hübner,1796近似,但雄性外生殖器抱器瓣端部略加宽,阳茎基环侧臂末端有齿,阳茎端膜具l根长粗刺,其基部一侧被3枚短刺.红纹细突野螟E似魄锄蠡之雄性外生殖器抱器瓣端部不加宽,阳茎基环侧臂末端无齿,阳茎端膜有3小刺束.正模♂,天津七里海,2001-09-09,尤平采,外生殖器玻片号GQl1075.副模:2♂♂,3♀♀,天津鸭淀,2001-08-04～ 2001-09-04,尤平采;10 ♂ ♂,3♀♀,山西省宁武县芦芽山保护区管理局,海拔1 450m,2011-07-19 ～24,郝淑莲、刘家宇采(外生殖器玻片号GQ11024 ♂,GQ11030♀,GQQQ1 1097 ♂);1 ♂,安徽泗县小良乡,2004-08-15,徐家生采(外生殖器玻片号GQ11028 ♂);1♂,安徽九华山柯村,2004-08-08,徐家生、张家亮采(外生殖器玻片号GQ11029♂).分布:中国(天津、山西、安徽).狭瓣细突野螟,新种Ecpy~horrhoe angustivalwaris sp.nov.(图4,7)本种与红纹细突野螟E.rud~indu Hübner,1796在外形上近似,但雄性外生殖器抱器腹背缘中部呈三角形突出,阳茎基环侧臂末端有齿,阳茎端膜有1簇短刺,角状器烟斗状.红纹细突野螟E r魄沈如之雄性外生殖器抱器腹背缘呈圆弧形突出,阳茎基环侧臂末端无齿,阳茎端膜有3小束刺,无角状器.正模♂,贵州麻阳河大河坝,海拔430m,2007-06-06,杜喜翠采,外生殖器玻片号GQ11081.分布:中国(贵州).     

中国红螯蛛属一新种(蜘蛛目,米图蛛科)

记述中国米图蛛科红螯蛛属1新种,膨胀红螯蛛Cheiracanthium inflatum sp.nov.,模式标本保存在河北大学博物馆.膨胀红螯蛛,新种Cheiracanthium inflatum sp.nov.(图1～14)正模♂,广西大明山自然保护区浣纱瀑布,2011年5月23日,王英楠采.副模:1♀,1♂,广西大明山自然保护区浣纱瀑布,2011年5月23日,彭艳秋采;1 ♂,广西大明山自然保护区龙腾宾馆附近,2011年5月29日,王英楠采.新种与短刺红螯蛛C.brevispinum Song et al,1982,岛红螯蛛C.insulanum (Thorell,1878)和彭妮红螯蛛C.pennyi O.P.-Cambridge,1873近似,但与后者的区别为:1)新种雄蛛中突较短呈刺状,而短刺红螯蛛中突较长且中央弯曲呈镰刀状,岛红螯蛛中突呈扁带状,彭妮红螯蛛中突较长呈钩状;2)新种雌蛛的纳精囊呈倒梨形,而短刺红螯蛛纳精囊略长呈肾形,岛红螯蛛纳精囊为球形,而彭妮红螯蛛纳精囊呈半球状.分布:中国广西.词源:新种种名源自拉丁词“inflatum”,指其膨胀的生殖球,形容词.     

海南岛斑舌甲属一新种记述(鞘翅目,拟步甲科,舌甲族)(英文)

记述斑舌甲属1新种,即海南斑舌甲Derispiahainanana sp.nov.,绘制了雄虫头部、前胸背板、鞘翅、足、腹部和阳茎特征图,并提供了体背、腹、侧面照片。模式标本保存于河北大学博物馆。海南斑舌甲,新种Derispia hainanana sp.nov.(图1~13)新种与D.octomaculata(Westwood,1883)在外形上相似,但可通过下列特征与后者区别:该种鞘翅有刻点;鞘翅侧缘由背面观可见基部4/5;阳基基板与阳基侧突近于等宽,基部弯曲,薄片状。正模♂,海南乐东尖峰岭,2006-07-12,王继良采。副模:5♂♂,5♀♀,标本信息同正模。词源:新种种名取自模式标本产地海南。     

新疆倍叉(虫责)属一新种记述(襀翅目:叉(虫责)科)

本文记述了采自新疆喀纳斯的倍叉[虫责]属Amphinemura 1新种：环齿倍叉[虫责]Amphinemura tricintusidens Wang＆Zhu,sp．nov。根据肛侧突中叶端部有3或4个环绕的小齿和肛上突背骨片端部形成的圆形腔可将该新种与其它种类相区别。正模♂,新疆喀纳斯,2005-Ⅷ—01,朱江艳等采。副模1♂,采集资料同正模。新种的模式标本保存在扬州大学昆虫标本馆。     

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.