中国渡濑氏鼠耳蝠种名订正

金黄鼠耳蝠Myotis formosus与渡濑氏鼠耳蝠M.rufoniger在物种识别及学名和中文名使用上一直混乱。以广东和江西采集的部分鼠耳蝠标本为研究对象,结合形态学和分子系统发育学方法对其进行分类厘定。结果显示,所采集的标本应为"渡濑氏鼠耳蝠",其形态特征却与国内文献中的"绯鼠耳蝠"(学名错用为M.formosus)形态描述相符合,结合历史文献,可确定国内鉴定的"绯鼠耳蝠"应为渡濑氏鼠耳蝠,国内分布区主要集中在中国东部,而近似种金黄鼠耳蝠仅在台湾和江西有分布记录。     

湖南长沙发现霍氏鼠耳蝠

2021年8月分别在湖南省长沙市天心区大托站立交桥底和昭华湘江大桥底捕获2只鼠耳蝠（2♂,标本号211521和211540）,经鉴定为霍氏鼠耳蝠（Myotis horsfieldii）,为湖南省蝙蝠分布新记录物种。本次捕获标本体型中等偏小,前臂长分别为36.1 mm（211521）和33.1 mm（211540）,头体长为44.0 mm和41.2 mm,后足长（10.5 mm和10.4 mm）超过胫骨长（16.4 mm和16.2 mm）的一半,耳屏长（5.1 mm和3.8 mm）不及耳长（12.5 mm和10.0 mm）的一半;头骨狭长,颅全长15.5 mm和15.0 mm,脑颅宽7.8 mm和7.5 mm,颅骨纤弱,额骨处有明显倾斜,脑颅高于上颌骨,颧弓较细。与来自泰国和印度尼西亚的霍氏鼠耳蝠标本相比,前臂长、头体长和尾长测量数据偏小,但头骨测量数据接近。基于Cyt b基因序列的系统发育分析表明,此次捕获的鼠耳蝠标本与霍氏鼠耳蝠聚类在一起,与来自香港的霍氏鼠耳蝠样本遗传距离仅为0.9%,故确定该物种为霍氏鼠耳蝠。标本保存于广东省科学院动物研究所。     

湖南省衡东县发现长指鼠耳蝠

2016年8月27日在湖南省衡阳市衡东县四方山林场仙妃洞（26°58′25″N,113°3′23″E,海拔463 m）采到1只鼠耳蝠标本（1♂）;同年8月29日在金觉峰（26°58′24.4″N,113°3′23.1″E,海拔311 m）采到9只鼠耳蝠标本（4♀,5♂）。上述鼠耳蝠标本形态较小,前臂长33.3 ~ 36.1 mm,其后足长（不包括爪长）长于胫长之半,胫外缘有毛;颅全长13.57 ~ 14.35 mm,头骨粗壮,脑颅圆且较高,明显高过上颌骨。经形态和线粒体Cyt b序列鉴定,确认这10只蝙蝠均为蝙蝠科（Vespertilionidac）鼠耳蝠属（Myotis）的长指鼠耳蝠（M. longipes）,该种为湖南省翼手目分布新记录种,标本（编号,4♀为HUNNU16JJ28、HUNNU16JJ42、HUNNU16JJ43、HUNNU16JJ52,6♂为HUNNU16SF25、HUNNU16JJ05、HUNNU16JJ08、HUNNU16JJ51、HUNNU16JJ58、HUNNU16JJ60）保存于湖南师范大学动物标本室。     

江西南昌及浙江衢州发现东亚水鼠耳蝠

2020年5至9月,在江西省南昌市向塘机场七里港火车桥底、高访立交桥底、横岗铁路桥底和浙江省衢州市衢州机场西山村涵洞分别捕获到1号(雌性)、4号(2雄性、2雌性)、2号(2雄性)和1号(雌性)鼠耳蝠。上述鼠耳蝠体型较小,头体长42.89 ~ 51.41 mm,前臂长40.18 ~ 42.22 mm;头骨较小,脑颅略低,顶部平缓,矢状脊不明显,吻长较短,吻宽较长,超过眶间宽,颧弓纤细且发达,宽度明显超过后头宽,明显区别于该地区已报道的鼠耳蝠物种。通过外部形态鉴定以及Cyt b、COI序列比对和系统发育关系结果,鉴定上述标本为东亚水鼠耳蝠(Myotis petax),且该种是在江西省和浙江省翼手目分布新记录种。上述标本保存于广东省科学院动物研究所。     

湖南衡东发现东亚水鼠耳蝠

2016年8月27日晚间在湖南省衡东县四方山国有林场仙妃洞(26°58′25″N,113°3′23″E,海拔463m)利用雾网采集到2号鼠耳蝠标本(HUNNU16SF16雄性、HUNNU16SF38雌性)。通过外部形态以及Cyt b序列比对,确认这两只鼠耳蝠为东亚水鼠耳蝠(Myotis petax)。此2个体体型较小,头体长分别为49.76 mm与49.93 mm,前臂长分别为40.73 mm和42.40 mm;头骨较小、略低而不显圆滑,上颌向上中等弯曲约30°,脑颅较低,顶部平缓,矢状脊不明显,吻较发达,宽度超过眶间宽,颧弓纤细,宽度明显超过后头宽,头骨后部略显浑圆而稍外凸;阴茎骨较长,1.088 mm,宽度为0.742 mm。此记录为湖南省翼手目分布新记录,标本保存于湖南师范大学脊椎动物标本馆。     

贵州省果树蹄蝠的分类记述

2008年10月在贵州省荔波县进行翼手目动物多样性调查中,于该县永康乡采集到2号蹄蝠标本,经与国内外记载过的蹄蝠科bicolor族群的标本进行比较,这2号标本的体型较小,前臂长分别为44.26mm、42.48mm,耳大而圆,耳长22.02mm、22.58mm;鼻叶简单,前鼻叶外侧没有小附叶,中鼻叶不发达;后鼻叶稍宽于前鼻叶和中鼻叶,被3纵隔分为4个部分,P2弱小,但未消失,位于齿列线外侧,这些特征与中国和泰国记载的果树蹄蝠Hipposideros pomona一致。另对贵州早期文献中记载的双色蹄蝠H.bicolor标本进行了查阅,认为其应归为果树蹄蝠。     

甘肃省卓尼县发现宽耳犬吻蝠

2020年10月17日,在甘肃省卓尼县（103°30′37″ E,34°35′00″ N,海拔2 540 m）用手网采集到1只雌性蝙蝠;该个体前臂长59.98 mm;两耳宽大,耳缘具毛,双耳前缘基部在额顶相联;吻部突出,上唇肥厚有褶皱;尾从尾膜后缘伸出一半;足掌具明显可见肉垫;各脚趾缘具有白色硬毛;背毛呈土褐色,毛基苍白色。头骨狭长,颅全长24.05 mm;颧弓平直;上门齿与上犬齿大,下门齿小,齿式为1.1.2.3/3.1.2.3 = 32。以上形态特征均与宽耳犬吻蝠（Tadarida insignis）相符;基于细胞色素b基因（Cyt b）系统发育学证据也支持上述结果,故将此标本鉴定为宽耳犬吻蝠。此为该种在甘肃省翼手目分布新记录。     

圆耳管鼻蝠在云南西双版纳的新发现

2019年4—5月利用蝙蝠竖琴网在云南省勐腊县龙林新村水沟采集到蝙蝠5只(3♀,2♂),中等偏小体型,鼻孔呈管状,耳廓较圆,外形、毛色和头骨特征与圆耳管鼻蝠Murina cyclotis相符,基于线粒体细胞色素氧化酶亚基Ⅰ基因(COⅠ)片段和核基因重组激活基因2基因(Rag2)片段构建的系统发育树均支持该鉴定结果,故确定该标本为圆耳管鼻蝠,为该种在云南省蝙蝠分布的新发现,标本现保存于广州大学生命科学学院。     

贵州发现毛翼管鼻蝠和华南菊头蝠及其回声定位声波特征

2017年5月分别在贵州省兴义市和安龙县用雾网采集到1只大体型雌性管鼻蝠和2只小体型雄性菊头蝠,经鉴定为毛翼管鼻蝠(Harpiocephalus harpia)和华南菊头蝠(Rhinolophus huananus),属贵州省翼手目新分布记录。所采集的毛翼管鼻蝠雌性个体可能为怀孕个体,故测量相关数据并鉴定后原地放归野外。华南菊头蝠标本保存于东北师范大学环境学院。毛翼管鼻蝠(1♀):鼻部呈短管状,全身被毛厚密而柔软,后足、翼膜和尾膜均被覆黄褐色绒毛;体重14.01 g,前臂长48.23 mm;回声定位声波为调频(FM)型,静止状态下声波峰频为(56.04±4.52)k Hz。华南菊头蝠(2♂):耳大,对耳屏相对较小;鼻叶之蹄状叶宽大,完全覆盖吻部;鞍状叶小,其高略超过其宽,近乎矩形;体毛烟褐色;2只样本体重分别为4.52 g、4.12 g,前臂长40.70 mm、40.00 mm;头骨狭长,颅全长16.35 mm、16.46 mm,颅宽8.11 mm、8.14 mm;回声定位声波属调频-恒频-调频(FM-CF-FM)型,静止状态下峰频分别为(68.48±0.08)k Hz、(67.18±0.06)k Hz。2种蝙蝠物种在贵州省为首次发现,扩大了其在国内的分布范围,丰富了生态资料,为进一步的研究和保护提供了基础资料。     

湖南省衡东县发现大卫鼠耳蝠

2015年7月26日于湖南省衡东县四方山仙妃洞(26°58′24.93″N,113°3′23.03″E,海拔641 m)捕到1只雌性蝙蝠。该蝙蝠体型较小,前臂长34.54 mm,后足长超过胫长的一半;通体黑褐色,被毛毛尖染有淡棕色,腹毛由前而后淡棕色毛尖逐渐增加,到腹后部几乎形成淡棕色区;颅全长13.34 mm,齿式为2.1.3.3/3.1.3.3=38,初步鉴定为大卫鼠耳蝠(Myotis davidii)。基于线粒体Cyt b基因1 140 bp序列对上述标本与大卫鼠耳蝠不同种群进行系统发育分析,大卫鼠耳蝠是一个单起源的谱系,其种群形成了广东、广西一个支系和江苏、安徽、浙江、湖南、重庆另一个支系,其中,江苏种群和广西种群之间的遗传距离最远。通过形态特征和线粒体Cyt b基因序列鉴定,确认此标本为蝙蝠科(Vespertilionidac)鼠耳蝠属的大卫鼠耳蝠。标本保存于湖南师范大学脊椎动物标本馆。     

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.