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1.
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 bCOI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。  相似文献   

2.
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。  相似文献   

3.
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。  相似文献   

4.
2022年7月和9月,本研究组在湖南开展翼手目多样性资源调查时,于常德市桃源县、湘西州保靖县、永州市双牌县和邵阳市绥宁县使用蝙蝠竖琴网分别采集到9只鼠耳蝠(7♂,2♀)和5只管鼻蝠(2♂,3♀),结合传统形态学和分子系统发育学方法对上述标本进行物种鉴定。该批鼠耳蝠体型中等,前臂长43.41~50.89 mm,全身毛发呈红褐色,耳廓端部、鼻孔周围、五趾与爪及尾末端均呈黑褐色,翼膜掌指间有三角形状的红褐色斑直达翼缘;头骨顶部平缓,颧弓发达,脑颅高而凸显,其形态特征和度量数据均与渡濑氏鼠耳蝠(Myotis rufoniger)相符。同时,采集的管鼻蝠标本体型中等,前臂长33.83~37.53 mm,背毛棕褐色,腹毛呈浅黄色;颅全长16.74~17.29 mm,颧弓平直而宽厚,其外形特征和度量数据均与中管鼻蝠(Murinahuttoni)相符。基于Cytb和COI基因构建的系统发育树均支持以上形态学鉴定结果。该报道为渡濑氏鼠耳蝠和中管鼻蝠在湖南省分布的新发现。标本现存于广州大学华南生物多样性保护与利用重点实验室,其中渡濑氏鼠耳蝠标本号为GZHU22429、GZHU22430、GZHU 2245...  相似文献   

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2015年7~9月在贵州省兴仁县、平坝县和兴义市的五屯镇及敬南镇捕获鼠耳蝠33只,鉴定为高颅鼠耳蝠(Myotis siligorensis),为贵州省新纪录物种。标本保存于贵州师范大学生命科学学院生态实验室。主要特征:体型较小,前臂长(36.03±1.50)mm(32.66~38.98 mm,n=33);耳狭长;耳屏直而细长;第Ⅲ掌骨最长,第Ⅴ掌骨最短;阴茎长(4.52±0.84)mm(2.85~5.75 mm,n=21);头骨狭长,颅骨凸显;颅全长(13.87±0.74)mm(13.00~14.88 mm,n=8),颅高(6.36±0.24)mm(6.03~6.74 mm,n=8);听泡较小;矢状脊细弱;上颌第1、2门齿向中央倾斜,上颌第1门齿有1个主尖和1个附尖;上颌第2门齿较第1门齿小,且与犬齿分离;上颌第2前臼齿(P3)位于齿列中。基于Cyt b基因(1 141 bp)序列进行的分子系统学分析显示,此次捕获鼠耳蝠物种与高颅鼠耳蝠聚在一起,二者遗传距离最近(仅为0.03),进一步确认所采集物种为高颅鼠耳蝠。  相似文献   

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2013年7月在广东南岭国家级自然保护区阳山县境内(24°48′39.5′′N,112°51′01.3′′E,海拔155 m)捕捉到4只雄性蝙蝠,体型小,前臂长34.1~34.7 mm,颅全长14.3~14.7 mm;体毛浓密,背毛毛基黑色,毛尖灰色,腹毛黑或棕色,毛尖奶油白,靠近肛门处腹毛浅灰色,些许白色;翼膜附着于跖部末端;后足特别延展,长度超过胫骨长之半;鉴定为长指鼠耳蝠[Myotis longipes(Dobson1873)]。同时,基于Cyt b基因序列(1 140 bp)构建的部分鼠耳蝠物种系统进化关系,进一步确认上述标本为长指鼠耳蝠,为广东省翼手目新纪录。该种蝙蝠在我国贵州、广西、重庆有分布记载,但标本和相关资料很少。本文给出了长指鼠耳蝠的外形和头骨特征测量数据,并与印度的标本进行了对比。长指鼠耳蝠的回声定位声波为调频型(FM),主频率为68.2 k Hz;此外,对其分类地位和分布状况进行了讨论。标本保存于广东省生物资源应用研究所。  相似文献   

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2013年4月在湖北省十堰市房县野人洞(31°55'8.3″N,110°43'56.5″E,海拔282 m)捕捉到11号鼠耳蝠标本(5雄6雌),同时在江苏省宜兴市灵谷洞(31°13'20.9″N,119°44'23.3″E,海拔123 m)捕捉到5号鼠耳蝠标本(1雄4雌)。上述鼠耳蝠标本体型较小,前臂长33.6~37.5 mm,颅全长11.2~13.8 mm;后足长不及胫骨长之半;背毛基部黑色,毛尖棕色有时更多显现浅红灰色,腹毛基部黑色但毛尖淡灰白;上颌前臼齿(P3)位于齿列之中。经鉴定均为尼泊尔鼠耳蝠(Myotis nipalensis),分别为湖北省和江苏省翼手目新纪录。本文给出了尼泊尔鼠耳蝠的外形和头骨特征及其相关测量数据,并与来自青海、尼泊尔的标本进行了对比;同时对其回声定位信号进行室内录制及分析;此外对其分类地位和分布状况进行了讨论。标本保存于广东省昆虫研究所。  相似文献   

8.
周全  张燕均  杨平  杨奇森  吴毅 《四川动物》2012,31(2):287-289
1984年9月24日在广东连州采集到2只蝙蝠(1♀,1♂),体型大,头体长分别为92.0mm,85.0mm,前臂长73.2mm,73.0mm,颅全长24.68mm,23.97mm;尾端有少量长毛;脑颅比较狭窄。经与国内已采集的黑髯墓蝠Taphozous melanopogon标本及已报道的同类蝙蝠特征相比较,鉴定该蝙蝠标本为鞘尾蝠科的大墓蝠Taphozous theobaldi Dobson,1872,为广东省蝙蝠新纪录种。  相似文献   

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对四川产中菊头蝠喜马拉雅亚种(Rhinolophus affinis himalayanus)和马铁菊头蝠日本亚种(R.ferrumequinum nippon)的23项外部形态指标和22项头骨形态指标进行了测量,并进行数理统计分析。结果表明,(1)中菊头蝠喜马拉雅亚种和马铁菊头蝠日本亚种的23项外部形态测量指标中有2项差异显著(P<0.05),16项差异极显著(P<0.01),其中:中菊头蝠喜马拉雅亚种(n=14)体长小于59 mm(47.30~58.40),尾长小于26 mm(21.69~25.68),耳长小于22 mm(18.36~21.88),前臂长小于56 mm(50.9~54.20),第Ⅲ掌骨第一指节长小于16 mm(13.2~15.53),第Ⅲ掌骨第二指节小于32 mm(27.38~31.74);而马铁菊头蝠日本亚种(n=6)体长大于62 mm(62.43~66.76),尾长大于30 mm(30.56~36.18),耳长大于24 mm(24.47~27.20),前臂长大于56 mm(58.78~63.46),第Ⅲ掌骨第一指节大于19 mm(19.38~21.39),第Ⅲ掌骨第二指节大于34 mm(34.42~38.11),这些差异可作为区分四川产这两个种的依据。(2)中菊头蝠喜马拉雅亚种和马铁菊头蝠日本亚种的22项头骨形态测量指标中,除颅高、听泡间距差异不显著(P>0.05)外,其他20项指标都存在极显著差异(P<0.01)。  相似文献   

10.
湖南省衡东县发现大卫鼠耳蝠   总被引:1,自引:0,他引:1  
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。  相似文献   

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Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.  相似文献   

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正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases  相似文献   

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The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.  相似文献   

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Some closely related members of the monocotyledonous familiesAlismataceae, Liliaceae, Juncaceae, Cyperaceae, Poaceae andAraceae with variable modes of pollination (insect- and wind-pollination) were studied in relation to the ultrastructure of pollenkitt and exine (amount, consistency and distribution of pollenkitt on the surface of pollen grains). The character syndromes of pollen cementing in entomophilous, anemophilous and intermediate (ambophilous or amphiphilous) monocotyledons are the same in principal as in dicotyledons. Comparing present with former results one can summarize: 1) The pollenkitt is always produced in the same manner by the anther tapetum in all angiosperm sub-classes. 2) The variable stickiness of entomophilous and anemophilous pollen always depends on the particular distribution and consistency of the pollenkitt, but not its amount on the pollen surface. 3) The mostly dry and powdery pollen of anemophilous plants always contains a variable amount of inactive pollenkitt in its exine cavities. 4) A step-by step change of the pollen cementing syndrome can be observed from entomophily towards anemophily. 5) From the omnipresence of pollenkitt in all wind-pollinated angiosperms studied one can conclude that the ancestors of anemophilous angiosperms probably have been zoophilous (i.e. entomophilous) throughout.
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正Dear Editor,Parainfluenza virus 5 (PIV5), known as canine parainfluenza virus in the veterinary field, is a negative-sense,nonsegmented, single-stranded RNA virus belonging to the Paramyxoviridae family (Chen 2018). The virus was first reported in primary monkey kidney cells in 1954 (Hsiung1972), then it has been frequently discovered in various  相似文献   

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