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1.
西南鼠耳蝠广东新纪录及其核型   总被引:1,自引:0,他引:1  
<正>西南鼠耳蝠(Myotis altarium Thomas,1911),因峨眉山为其模式产地,又称峨眉鼠耳蝠或者四川鼠耳蝠。隶属于翼手目(Chiroptera)蝙蝠科(Vespertilionidae)鼠耳蝠属(Myotis),主要分布  相似文献   

2.
绯鼠耳蝠Myotis formosus又称丽鼠耳蝠、红黑鼠耳蝠等,隶属于翼手目Chiroptera蝙,蝠科Vespertilionidae蝙蝠亚科Vespertilioninae鼠耳蝠属Myotis.2006年12月20日于河南省南阳市桐柏山熊洞(2°62′N,113°68′E,海拔301 m)发现一冬眠群共31只色彩鲜艳的蝙蝠,仅采集5只,外形测量后分离头骨,毛皮做成剥制标本保存于河南师范大学生命科学学院标本馆.经进一步鉴定,确定为绯鼠耳蝠华南亚种Myotis formous rufoniger,为河南省蝙蝠新纪录.  相似文献   

3.
大足鼠耳蝠的翼型和回声定位声波特征   总被引:1,自引:1,他引:0  
大足鼠耳蝠(Myotis ricketti Thomas,1894)属翼手目(Chiroptera),蝙蝠科(Vespertilionidae),鼠耳蝠属(Myotis).  相似文献   

4.
水鼠耳蝠 Myotis daubentonii(Chiroptera,Vespertilionidae),广泛分布于欧洲和亚洲,亚种分化众多,在亚洲已报道有 M.d.ussuriensis,M.d.loukashkini,M.d.petax和M.d.laniger但其分类地位一直受到国内外学者的关注.中国的水鼠耳蝠长期以来被认为属于水鼠耳蝠M daubentonii亚种.最近有研究认为中国的水鼠耳蝠与欧洲的水鼠耳蝠M.daubentonii不同,并把"petax"提升为种.在中国境内相继采到17只鼠耳蝠标本,根据外形、头骨、牙齿、阴茎骨、线粒体DNA细胞色素b等特征,鉴定为东亚水鼠耳蝠Myotis petax,对中国水鼠耳蝠的种和亚种分类做一讨论.  相似文献   

5.
使用肺、心脏等组织进行培养,用空气干燥法制作染色体标本,以胰酶法制作G带,BSG法制作c带,分析了贵州2种鼠耳蝠的核型、G带和c带.水鼠耳蝠Myotis daubentoni和小鼠耳蝠Myotis dividii的染色体数均为2n=44,拥有3对大型和1对中型中着丝粒染色体,染色体臂数(FN)=52;这2种鼠耳蝠的G带...  相似文献   

6.
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。  相似文献   

7.
对肺、心等进行组织培养,用空气干燥法制作染色体标本,对贵州3种蝙蝠即中华鼠耳蝠(Myotis chinensis)、西南鼠耳蝠(M.altarium)和亚洲长翼蝠(Miniopterus fuliginosus)进行了G-带、C-带带型分析。结果表明,2种鼠耳蝠的G-带基本相同,亚洲长翼蝠的G-带与两种鼠耳蝠有一定同源性;C-带核型中,中华鼠耳蝠和亚洲长翼蝠只有着丝粒带,而西南鼠耳蝠有的染色体有插入C-带和端位C-带。根据带型异同分析讨论了鼠耳蝠和长翼蝠间的进化关系。  相似文献   

8.
广东7种蝙蝠的核型研究   总被引:1,自引:0,他引:1  
吴毅  原田正史 《兽类学报》2006,26(4):403-406
对采集于广东的4科7种蝙蝠进行了核型分析,它们的核型分别是:犬蝠(Cynopterus sphinx)2n=34,FN=58;印度假吸血蝠(Megaderma lyra)2n=54,FN=104;大耳双色蹄蝠(Hipposideros pomona)2n=32,FN=60;中蹄蝠(H.larvatus)2n=32,FN=60;大卫鼠耳蝠(Myotis davidii)2n=46,FN=52;大黄蝠(Scotophilusheathi)2n=36,FN=54;南长翼蝠(Miniopterus australis)2n=46,FN=50。其中大耳双色蹄蝠和大卫鼠耳蝠的核型为首次报道,犬蝠、印度假吸血蝠、中蹄蝠、大黄蝠和南长翼蝠的核型为中国第一次报道。  相似文献   

9.
2005 ~2009年,野外采集大卫鼠耳蝠(Myotis davidii)的回声定位声波、翼型数据及粪便样本,分析了其回声定位声波、翼型特征和夏季食性.结果表明,大卫鼠耳蝠回声定位声波主频为(60.4±10.0)kHz (Mean±SD),带宽为(54.7±8.5)kHz,能率环为7.4%±3.5%;翼展比为6.2±0...  相似文献   

10.
于湖南省永州市铜岩洞采集到14只蝙蝠,经鉴定为大足鼠耳蝠(Myotis ricketti),为湖南省翼手目新纪录.本文报道了该物种体型和头骨特征,并与浙江和安徽样本进行比较.大足鼠耳蝠发出典型的下扫调频声波,其低峰频、短时程的声波特征以及强壮的后足和锋利的爪等形态特征与其在水面"拖网式(trawhng)"捕食鱼类的捕食...  相似文献   

11.
Nucleotide sequences of the mitochondrial cytochrome b gene are reported from bats of the genus Myotis including species of the endemic southern African subgenus Cistugo, Myotis (Cistugo) sebrai and Myotis (Cistugo) lesueuri. We also examined Myotis annectans from Southeast Asia, and Myotis macropus from Australia. The two species of Cistugo and Myotis annectans represent the only species of Myotis to differ in chromosome number from the common 2n=44 found in >40 species. Our results show that the two species of Cistugo are more divergent from the other species of Myotis than several other well-recognized genera and we recommend elevating Cistugo to full generic rank. Myotis annectans groups well within Myotis, clustering with other Southeast Asian and Japanese species, and thus represents the only species of Myotis known to have diverged from the common 2n=44 karyotype. Myotis macropus clusters within a clade that includes Southeast Asian species.  相似文献   

12.
The genus Myotis includes the largest number of species in the family Vespertilionidae (Chiroptera), and its members are distributed throughout most of the world. To re-evaluate the phylogenetic position of East Asian Myotis species with respect to Myotis species worldwide, we analyzed mitochondrial gene sequences of NADH dehydrogenase subunit 1 and cytochrome b from 24 East Asian individuals as well as 42 vespertilionid bats determined previously. The results suggest that: (1) some individuals having the same species name in Europe and Japan do not form a monophyletic clade, indicating that some bat species exhibit morphological convergence, (2) Japanese Myotis mystacinus forms a sister relationship with Myotis brandtii (Palaearctic), and both species are included in the American clade implying that an ancestor of these species originated in North America, and (3) the Black whiskered bat, Myotis pruinosus, is endemic to Japan and forms sister relationships with Myotis yanbarensis and Myotis montivagus collected from Okinawa (Japan) and Selangor (Malaysia), respectively, implying that M. pruinosus originated from the south. The systematics of Japanese and East Asian Myotis bats were revisited by considering their phylogenetic relationships. Our study provides the first extensive phylogenetic hypothesis of the genus Myotis that includes East Asian and Japanese species.  相似文献   

13.
毛腿鼠耳蝠(Myotis fimbriarus)血液的研究   总被引:1,自引:0,他引:1  
本文对毛腿鼠耳蝠血液的有形成分和百分比等项正常数值进行了测定,并对各类血细胞的主要形态作了描述。 所测的各项数值与前人报道的数据比较,其红细胞数目和血红素含量都高于同属的其他种,也较其他哺乳动物为高。毛腿鼠耳蝠与该属有些种类的淋巴细胞数目占全部白细胞的百分数最高,也明显高于其他哺乳动物。  相似文献   

14.
The diets of British bats (Chiroptera)   总被引:4,自引:0,他引:4  
Sixty-one studies of the diets of 15 species of bats found in the British Isles are reviewed. Fourteen studies describe the diets of more than one species. Barbastella barbastellus and Plecotus spp. eat mainly Lepidoptera. Eptesicus serotinus takes mainly Coleoptera, but feeds on a wide range of prey, found in several habitats. Rhinolophus ferrumequinum hunts mainly Coleoptera and Lepidoptera by hawking, gleaning and perch hunting. Myotis bechsteinii takes mostly woodland families of Diptera and Lepidoptera. The remaining nine species eat mainly Diptera. Myotis nattereri feeds almost entirely on diurnal Diptera, gleaned from their nightly resting places. Rhinolophus hipposideros and Myotis mystacinus take mostly swarming crepuscular Diptera by hawking, probably near water and in damp wooded areas; both also glean. Myotis brandtii feeds on Diptera by hawking and gleaning; Nyctalus noctula by hawking. Myotis daubentonii, Pipistrellus spp. and Nyctalus leisleri eat many aquatic Diptera, and may therefore be expected to feed close to freshwater habitats. M. daubentonii hunts by trawling aquatic Diptera from the surface of water.  相似文献   

15.
The bat Myotis adversus hunts for prey by aerial hawking and by taking prey from the water surface with its feet (trawling). The flight performance and echolocation of this species were studied in Queensland, Australia, and comparisons were made with Myotis daubentoni , a bat filling a similar ecological niche in the Palaearctic Region. The bats foraged in very similar ways, using the same foraging tactics and feeding in similar habitats, yet they were not geometrically similar in shape. The slightly larger Myotis adversus had relatively larger wings than M. daubentoni , conferring a slightly lower wing-loading. Nevertheless, M. adversus flew faster than M. daubentoni during the searching phase of foraging. Myotis daubentoni turned in tighter circles than M. adversus . Both species used short frequency-modulated (FM) echolocation calls of a characteristic sigmoidal structure, and nulls typically observed in the calls were an observational artefact. Myotis adversus also adopted an unusual 'long'FM call while foraging. The relations between echolocation frequencies and body size were explored in male M. adversus . Specialized morphological and acoustic adaptations for prey capture by trawling in insectivorous bats are discussed.  相似文献   

16.
何淑艳  敖磊  李娜  谷晓明 《四川动物》2007,26(3):520-524
对贵州5种蝙蝠科蝙蝠的部分线粒体细胞色素氧化酶亚基ⅠDNA序列进行了测定,并结合从Genbank获得的爪哇伏翼的相应序列,以Pteropus dasymallus,P.scapulatus,Rousettus aegyptiacus为外群,运用贝叶斯法(Bayes-ian),最大似然法(Maximum Likelihood,ML)分析了这6种蝙蝠科蝙蝠的分子系统进化关系。结果表明:在贝叶斯,ML树中,这6种蝙蝠科的蝙蝠可分为3个分支:亚洲长翼蝠是第1个独立出来的分支;白腹管鼻蝠是继亚洲长翼蝠之后第2个分离出来的分支;第3个分支又分为两支,一支由大鼠耳蝠和小鼠耳蝠组成,另一支由南蝠和爪哇伏翼组成,支持将这4种蝙蝠同归于蝙蝠亚科的结论,从一定程度上否定了鼠耳蝠属和管鼻蝠亚科之间的姐妹类群关系,也不支持将鼠耳属提升为亚科。  相似文献   

17.
Based on extensive phenetic analyses, bats of the genus Myotis have been classically subdivided into four major subgenera each of which comprise many species with similar morphological and ecological adaptations. Each subgenus thus corresponds to a distinct "ecomorph" encompassing bat species exploiting their environment in a similar fashion. As three of these subgenera are cosmopolitan, regional species assemblages of Myotis usually include sympatric representatives of each ecomorph. If species within these ecomorphs are monophyletic, such assemblages would suggest extensive secondary dispersal across geographic areas. Conversely, these ecomorphological adaptations may have evolved independently through deterministic processes, such as adaptive radiation. In this case, phylogenetic reconstructions are not expected to sort species of the same ecomorph into monophyletic clades. To test these predictions, we reconstructed the phylogenetic history of 13 American, 11 Palaearctic, and 6 other Myotis species, using sequence data obtained from nearly 2 kb of mitochondrial genes (cytochrome b and nd1). Separate or combined analyses of these sequences clearly demonstrate the existence of several pairs of morphologically very similar species (i.e., sibling species) which are phylogenetically not closely related. None of the three tested subgenera constitute monophyletic units. For instance, Nearctic and Neotropical species currently classified into the three subgenera were clustered in a single, well-supported monophyletic clade. These species thus evolved independently of their ecological equivalents from the Palaearctic region. Independent adaptive radiations among species of the genus Myotis therefore produced strikingly similar evolutionary solutions in different parts of the world. Furthermore, all phylogenetic reconstructions based on mtDNA strongly supported the existence of an unsuspected monophyletic clade which included all assayed New World species plus M. brandtii (from the Palaearctic Region). This "American" clade thus radiated into a morphologically diverse species assemblage which evolved after the first Myotis species colonized the Americas. Molecular reconstructions support paleontological evidence that species of the genus Myotis had a burst of diversification during the late Miocene-early Pliocene epoch.  相似文献   

18.
Habitat restoration is an integral feature of wildlife conservation. However, funding and opportunities for habitat restoration are limited, and therefore, it is useful for targeted restoration to provide positive outcomes for non‐target species. Here, we investigate the possibility of habitat creation and management benefitting two threatened wetland specialists: the Green and Golden Bell Frog (Litoria aurea) and the Large‐footed Myotis (Myotis macropus). This study involved two components: (i) assessing co‐occurrence patterns of these species in a wetland complex created for the Green and Golden Bell Frog (n = 9) using counts, and (ii) comparing foraging activity of Large‐footed Myotis in wetlands with low and high aquatic vegetation (n = 6 and 7, respectively) using echolocation metres. Since Large‐footed Myotis possesses a unique foraging behaviour of trawling for aquatic prey, we hypothesised that foraging activity of this species would be higher in wetlands with low aquatic vegetation coverage. Additionally, we provide observations of its potential prey items. We identified one created wetland where both species were found in relatively high numbers, and this wetland had a permanent hydrology, was free of the introduced fish Gambusia (Gambusia holbrooki) and had low aquatic vegetation coverage. We also found that Myotis feeding activity was significantly higher in low aquatic vegetation coverage wetlands (x? = 65.72 ± 27.56 SE) compared to high (x? = 0.33 ± 0.33 SE, P = 0.0000). Although this is a preliminary study, it seems likely that Green and Golden Bell Frog and Large‐footed Myotis would gain mutual benefit from wetlands that are constructed to be permanent, that are Gambusia free, low in aquatic vegetation coverage, and are located in close to suitable roosting habitat for Large‐footed Myotis. We encourage adaptive aquatic vegetation removal for Green and Golden Bell frog as this may have benefits for Large‐footed Myotis. The evidence suggests that the former may be a suitable umbrella species for the latter.  相似文献   

19.
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