基于12S和16S rRNA序列的湍蛙属部分物种的系统发育关系

测定了湍蛙属 6个种共 10个种群 ,以及 4个外群种的线粒体 12S和 16SrRNA基因片段 ,比对后有94 0bp序列 ,发现 35 2个变异位点、 186个简约性位点。运用NJ法、MP法、ML法构建了系统关系树 ,各系统树一致表明内群为一单系群 ,分为两组 :第一组中 ,四川湍蛙两种群先聚合 ,再和棕点湍蛙聚为一支 ;第二组中 ,香港湍蛙和戴云湍蛙聚为一支 ,而香港大屿山离岛湍蛙种群首先与华南湍蛙相聚 ,再与武夷湍蛙构成姐妹支。研究结果表明 :香港地区增加 1种湍蛙分布 ;戴云湍蛙是一有效种 ;四川湍蛙的石棉和洪雅种群间遗传差异达到或超过其他种间的分歧水平。     

中国林蛙的分子系统关系

测定了 6种林蛙和用作外群的 2种侧褶蛙和 1种陆蛙的线粒体 12SrRNA基因序列 393bp。序列两两对位比较表明内外群间的位点替换率是 7 3%到 2 3 1% ,内群中物种间则为 0 0 %到 9 2 %。依据上述DNA序列 ,用距离法和最大简约法的系统发育分析表明 :①研究的 6种林蛙聚为一支 ,构成单系群 ,并有高的BPs值(90 %以上 )支持 ;② 6种林蛙可以分成 2个姐妹群 ,即中国林蛙、黑龙江林蛙和桓仁林蛙为一组 (BPs >94% ) ,峨眉林蛙、昭觉林蛙和镇海林蛙为一组 (BPs >5 0 % ) ;③昭觉林蛙与镇海林蛙有较近的亲缘关系 ;④中国林蛙的榆中种群与牡丹江种群间的遗传分化似乎达到了种级分化水平。     

我国臭蛙属(两栖纲:蛙科)的系统发育

为探讨臭蛙属的种间亲缘关系与其起源和分化,采用PAUP3．1软件对我国的16种臭蛙的29项分类性状进行系统发育关系的研究。结果表明,臭蛙属物种形成1个单系群,可以划分为4个种组;表明了臭蛙属中国物种间的亲缘关系;无指盘臭蛙和云南臭蛙是本属中最原始的物种,鸭嘴臭蛙等是较特化的物种;原始臭蛙可能起源于横断山区和云南西部高原,贵州高原可能是臭蛙的分化中心;各种组内相近种的地理替代呈南北方向更替,而种组间则呈东西方向更替;原始物种多分布于中国西南部,较进化或特化物种多分布于中国东部和东南部及海岛上;其种组亲缘关系与地理分布格局显示出一致性。     

江西赣江源区域两栖动物的群落组成和物种多样性特征

赣江发源于武夷山脉南段西麓的高山岭间,该区域独特的地理环境和气候特征蕴育了丰富的生物多样性。然而关于该区域两栖动物群落组成和物种多样性调查非常匮乏,不利于赣江源头两栖动物物种多样性的保护。于2016年4-9月期间在江西赣江源区域采用样线法调查了两栖动物的资源状况、群落组成及物种多样性特征,比较了它们在山地森林区、丘陵森林与农田区和盆地农田区3类栖息地之间的差异性。结果表明：赣江源区域分布有8科23种两栖动物,新增记录3个物种,包括尖舌浮蛙、寒露林蛙和九龙棘蛙,泽陆蛙和饰纹姬蛙为优势种。赣江源区域的两栖动物群落组成和物种多样性存在显著的季节间差异和栖息地间差异;两栖动物季节性繁殖是造成前者差异的主要因素,而土地利用类型、栖息地特征、空间距离、生活习性的物种特性等因素成就了后者差异的出现。因此,春、夏季一般有比秋季见到更高的两栖动物物种丰富度和多样性;山地森林区的两栖动物物种丰富度和多样性最高,盆地农田区次之,丘陵森林与农田区的最低。山地森林区应成为赣江源区域两栖动物多样性保护的优先区域。国家Ⅱ级重点保护野生动物虎纹蛙,在3类栖息地中均有分布,且在盆地农田区和山地森林区能见到更多个体,但农田区分布的虎纹蛙遭受到更大的威胁,建议加强对农田区虎纹蛙及其栖息地的保护。     

从12S rRNA基因片段序列研究20种蛇的系统发生关系

本文测定了中国产蛇亚目20种蛇约800bp的mtDNA 12S rDNA基因片段序列。所测序列与楔齿蜥的同源序列一起经Clustal X1.8软件比对,共有881个位点,其中变异位点有494个。以楔齿蜥为外群,用NJ法构建了4科20种蛇的进化关系树,对这20种蛇的系统发生关系作了初步探讨。研究结果表明：所研究的4个科20种蛇分成4个支系。第一个支系包括蟒科的东方沙蟒和蟒2种蛇;第二个支系为蝰科3种蛇,即草原蝰、尖吻蝮、竹叶青组成一个单系群;眼镜蛇科的眼镜蛇和银环蛇构成第三个支系;游蛇科的13种蛇构成了第四个支系,其中灰鼠蛇、乌梢蛇和赤链蛇组成一个支系,锦蛇属的7种蛇组成一个单系群,然后它们与前一支系相聚。剩下的颈槽蛇属两种聚类后与赤链华游蛇构成一个支系,并与游蛇科其它蛇组成姐妹群。第四支系首先与第三支系眼镜蛇科聚类,第二支系蝰科构成了三、四支系眼镜蛇科和游蛇科的姐妹群,第一支系蟒科在系统树的最基部,为四个科中较原始的类群。     

倭蛙属(无尾目∶蛙科)肩带研究

对倭蛙属(Nanorana)已知3种:高山倭蛙(Nanorana parkeri)、倭蛙(N.pleskei)和腹斑倭蛙(N.ventripunctata)的肩带作了连续切片后进行Masson染色,发现其上喙骨(epicoracoid)的融合与重叠的状况与虎纹蛙(Rana rugulosa)较相似,而与无尾目中其它物种已知的肩带形态存在较大的差异。倭蛙属和虎纹蛙等与已知肩带类型的蛙亚科其它的物种在系统进化中可能来源于不同的最近共同祖先。     

倭蛙属(无尾目:蛙科)肩带研究

对倭蛙属（Nanorana）已知3种：高山倭蛙（Nanorana parkeri）、倭蛙（N. pleskei）和腹斑倭蛙（N. ventripunctata）的肩带作了连续切片后进行Masson染色,发现其上喙骨（epicoracoid）的融合与重叠的状况与虎纹蛙（Rana rugulosa）较相似,而与无尾目中其它物种已知的肩带形态存在较大的差异.倭蛙属和虎纹蛙等与已知肩带类型的蛙亚科其它的物种在系统进化中可能来源于不同的最近共同祖先.     

中国无尾两栖类新记录种——朝鲜侧褶蛙北大核心CSCD

2021年9月在沈阳市蒲河湿地公园(41°41′54″N,122°52′19″E,海拔35 m)采集到3号无尾两栖类动物,经形态特征比较确认为侧褶蛙属(Pelophylax)金线侧褶蛙种组(P.plancyi species complex)的物种。基于线粒体12S rRNA和16S rRNA基因联合构建的侧褶蛙属部分物种最大似然系统发育树显示,采集到的侧褶蛙标本与朝鲜侧褶蛙(P.chosenicus)聚为一支,且具有较高的支持率(0.95)。综合形态和系统发育比较,确定采集到的标本为无尾目(Anura)蛙科(Ranidae)侧褶蛙属的朝鲜侧褶蛙,系中国两栖动物分布新记录种。     

基于12S rRNA基因序列探讨凹耳蛙(无尾目,蛙科)的分类地位

为探讨凹耳蛙Rana tormotus的分类地位,测定了凹耳蛙线粒体12S rRNA基因序列,并从GenBank中下载了蛙科33种蛙的同源序列进行分析,用BI法、NJ法和MP法构建分子系统树.结果表明:3种树拓扑结构基本一致,都显示凹耳蛙与长吻胡湍蛙Huia nasica亲缘关系最近,凹耳蛙与长吻胡湍蛙相聚后再与臭蛙Odorrana组成单系群,而与湍蛙Amolops亲缘关系较远.据此,支持将该蛙从湍蛙属划出,并建议归入臭蛙属.     

新疆蛙类遗传多样性与系统发育研究

[目的]为了解新疆地区中国林蛙中亚林蛙、中亚侧褶蛙和阿尔泰林蛙的遗传多样性及系统发育。[方法]分别于新疆7个地方采集了4种蛙类共53个个体,对线粒体12S RNA基因进行了扩增和测序。[结果]经过拼接和比对,得到长度为893 bp片段的序列,4种蛙类共定义了21个单倍型,其中,中国林蛙、中亚侧褶蛙和阿尔泰林蛙遗传变异程度高,而中亚林蛙的遗传变异很低。各群体总遗传分化系数Gst为0.367 88,总固定系数Fst为0.871 56,总基因流Nm为0.04。中国林蛙与中亚林蛙之间的遗传距离最大,为0.158,与中亚侧褶蛙之间的遗传距离次之,为0.137,与阿尔泰林蛙之间遗传距离最小,为0.034。聚类分析显示中国林蛙和阿尔泰林蛙聚为一支,中亚林蛙和中亚侧褶蛙聚为一支。[结论]新疆地区的中国林蛙、中亚侧褶蛙和阿尔泰林蛙的遗传多样性丰富,中亚林蛙的遗传多样性较低,各群体遗传分化程度较高。     

从线粒体基因探讨中国大头蛙群的分类及其属内地位

Partial sequences of the mitochondrial 12S rRNA and 16S rRNA gene were determined for 8 populations of three species of Chinese Limnonectes, and aligned with the published sequences of Limnonectes from other parts of the world. When Nanorana parker, Paa boulengeri, Fejervarya limnocharis and Hoplobatrachus rugulosus was used as outgroup taxa (Accession Nos. AY158705, AY313685, AF206111, AF206491, AY322311). The sequences of the 12S rRNA and 16S rRNA genes totaled 950 nueleotide positions with gaps including 510 variable sites. We reconstructed phylogenetie trees using Clustal X 1.8, Mega 2.1 and PHYLIP 3.5e software, and using the maximum parsimony and maximum likelihood methods, respectively. Our analyses suggest that these fanged frogs from China are another monophyletie group in addition to the four monophyletie groups identified by previous studies. The Chinese Limnonectes were grouped into three elades (BCL 55% ). The first elade contains one species (BCL 100% ), from a population of Limnoneetes fragilis from Hainan Province. The second contains four individuals (BCL 100% ), i. e. two populations of Limnonectes kuhlii from Yunnan Province. The third contains one species (BCL 100% ), i. e. five populations of Limnonectes fujianensis from Fujian Province and 1 from Taiwan Province. The resulted phylogenetie trees indicate L. fragilis is basal to L. kuhlii L. fujianensis 。     

Molecular phylogeny of the ranid frogs from Southwest India based on the mitochondrial ribosomal RNA gene sequences

The Western Ghats of Southwestern India are known as one of the world's "hotspots" of biodiversity. We collected frog specimens from the family Ranidae and investigated the phylogenetic relationships among ranid species, particularly among the Fejervarya, a genus whose morphological diagnostic characteristics and phylogenetic features remain little known. We analyzed partial sequences of the mitochondrial 12S (428 bp) and 16S rDNAs (549 bp). Results showed that the members of Fejervarya form a monophyletic group with the genera Hoplobatrachus and Euphlyctis among ranid genera. This confirms the recent allocation of Fejervarya, including it within the subfamily Dicroglossinae. The mitochondrial rDNA data in our study also appeared to be useful as a marker to distinguish Fejervarya species without morphological differences. The phylogenetic tree based on the 16S rDNA sequence showed a correlation between Fejervarya phylogenies and their geographic distributions. Lastly, our results suggested the recent occurrence of a radiation event of Fejervarya species in the Indian-Sri Lankan region.     

The Chinese bamboo leaf odorous frog (Rana (Odorrana) versabilis) and North American Rana frogs share the same families of skin antimicrobial peptides

The Chinese bamboo leaf odorous frog (Rana (Odorrana) versabilis) and the North American pickerel frog (Rana palustris) occupy different ecological niches on two different continents with no overlap in geographical distribution. R. palustris skin secretions contain a formidable array of antimicrobial peptides including homologs of brevinin-1, esculentin-1, esculentin-2, ranatuerin-2, a temporin and a family of peptides considered of unique structural attributes when isolated, palustrins 1-3. Here we describe the structures of mature peptides and precursors of eight putative antimicrobial peptides from the skin secretion of the Chinese bamboo leaf odorous frog (Rana (Odorrana) versabilis). Each peptide represents a structural homolog of respective peptide families isolated from R. palustris, including two peptides identical in primary structure to palustrin 1c and palustrin 3b. Additionally, two peptides were found to be structural homologs of ranatuerin 2B and ranatuerin 2P from the closely-related North American species, Rana berlandieri (the Rio Grande leopard frog) and Rana pipiens (the Northern leopard frog), respectively. Both palustrins and ranatuerins have hitherto been considered unique to North American ranid frogs. The use of primary structures of amphibian skin antimicrobial peptides is thus questionable as a taxonomic device or alternatively, the micro-evolution and/or ancestry of ranid frogs is more highly complex than previously thought.     

Molecular systematics and biogeography of the fanged frogs of Southeast Asia

Our analysis of parts of the mitochondrial ribosomal 12S and 16S genes from 39 populations of Southeast Asian ranid frogs confirms that the fanged frogs are a monophyletic clade. This group, properly called Limnonectes, appears to have arisen in the early Tertiary at a time when free faunal exchange was possible among Southeast Asia, Borneo, Sumatra, Java, and, probably, Sulawesi. Four species groups are tentatively identified within the clade. Part of group 1 includes species related to L. kuhlii that occur in Borneo. Another part of group 1 includes species from Malay Peninsula and Thailand that are related to L. pileata. Species group 2, L. leporina, occurs only in Borneo. Species group 3 is restricted to species distributed in Sulawesi and the Philippines. Species group 4 includes L. blythii and relatives. There is a lack of compatibility between phylogenetic hypotheses generated from molecular and morphological data sets. These differences are related, in large part, to whether some species of Limnonectes have secondarily lost fangs or whether lack of fangs represents the primitive condition.     

Multiple invasions of the Ryukyu Archipelago by Oriental frogs of the subgenus Odorrana with phylogenetic reassessment of the related subgenera of the genus Rana

The genus Rana, notably diversified in Oriental regions from China to Southeast Asia, includes a group of cascade frogs assigned to subgenera Odorrana and Eburana. Among them, R. ishikawae and the R. narina complex represent the northernmost members occurring from Taiwan to the Ryukyu Archipelago of Japan. Relationships of these frogs with the continental members, as well as the history of their invasions to islands, have been unclear. The taxonomic status of Odorrana and related genera varies among authors and no phylogenetic reassessment has been done. Using partial sequences of mitochondrial 12S and 16S rRNA genes, we estimated phylogenetic relationships among 17 species of the section Hylarana including Odorrana and Eburana, and related species from the Ryukyus, Taiwan, China, Thailand, Malaysia, and Indonesia. We estimate that (1) Odorrana is monophyletic and encompasses species of Eburana and R. hosii, which is now placed in Chalcorana, (2) the ancestor of R. ishikawae separated from other Rana in the middle to late Miocene prior to its entry to the Ryukyu Archipelago, (3) the ancestor of the R. narina complex later diversified in continental Asia, and invaded the Ryukyu Archipelago through Taiwan, (4) the R. narina complex attained its current distribution within the Ryukyus through niche segregations, and (5) vicariance of R. hosii between Malay Peninsula and Borneo occurred much later than the divergence events in the R. narina complex. Current subgeneric classification of Rana, at least of Southeast Asian members, requires full reassessment in the light of phylogenetic relationships.     

Neighbor–Stranger Discrimination in Concave-Eared Torrent Frogs, Odorrana tormota

The dear enemy phenomenon in which animals discriminate familiar neighbors from unknown strangers, and respond more aggressively to strangers is well established in various social animals, especially in songbirds and mammals. So far, very few studies of neighbor–stranger discrimination have been carried out in amphibians and the results have been mixed. Thus, it is unclear whether this phenomenon exists commonly in frogs and toads, and whether it is exhibited by species with large vocal repertoires. We conducted acoustic playback experiments with male concave-eared torrent frogs ( Odorrana tormota , a species with an unusually large vocal repertoire) kept in a tank in a quiet room to investigate whether or not they can discriminate strangers from neighbors acoustically. Nine of the 14 males tested showed evoked vocal responses to the calls from strangers, but none to calls from neighbors; vocal response to the calls from strangers was accompanied by aggressive motor activity. These results demonstrate that male O. tormota possess the ability to discriminate neighbors from strangers acoustically. Odorrana tormota therefore joins three ranid species ( Rana catesbiana , Rana clamitans , Rana dalmatina , all known to have a comparatively small and stereotyped vocal repertoires) as the only anurans demonstrated to have this ability. Given the difference in signaling complexity between these frog species, the salient acoustic features used for discriminating neighbors and strangers are likely to be quite distinct.     

Three New Ranidae Mitogenomes and the Evolution of Mitochondrial Gene Rearrangements among Ranidae Species

Various types of gene rearrangements have been discovered in the mitogenoes of the frog family Ranidae.In this study,we determined the complete mitogenome sequence of three Rana frogs.By combining the available mitogenomic data sets from Gen Bank,we evaluated the phylogenetic relationships of Ranidae at the mitogenome level and analyzed mitogenome rearrangement cases within Ranidae.The three frogs shared an identical mitogenome organization that was extremely similar to the typical Neobatrachian-type arrangement.Except for the genus Babina,the monophyly of each genus was well supported.The genus Amnirana occupied the most basal position among the Ranidae.The[Lithobates+Rana]was the closest sister group of Odorrana.The diversity of mitochondrial gene arrangements in ranid species was unexpectedly high,with 47 mitogenomes from 40 ranids being classified into 10 different gene rearrangement types.Some taxa owned their unique gene rearrangement characteristics,which had significant implication for their phylogeny analysis.All rearrangement events discovered in the Ranidae mitogenomes can be explained by the duplication and random loss model.     

Out of Asia: Mitochondrial DNA Evidence for an Oriental Origin of Tiger Frogs, Genus Hoplobatrachus

Most examples of intercontinental dispersal events after the Miocene contact between Africa and Asia involve mammal lineages. Among amphibians, a number of probably related groups are known from both continents, but their phylogenies are so far largely unresolved. To test the hypothesis of Miocene dispersal against a Mesozoic vicariance scenario in the context of Gondwana fragmentation, we analyzed fragments of the mitochondrial 16S rRNA gene (572 bp) in 40 specimens of 34 species of the anuran family Ranidae. Results corroborated the monophyly of tiger frogs (genus Hoplobatrachus), a genus with representatives in Africa and Asia. The African H. occipitalis was the sister group of the Asian H. crassus, H. chinensis, and H. tigerinus. Hoplobatrachus was placed in a clade also containing the Asian genera Euphlyctis and Nannophrys. Combined analysis of sequences of 16S and 12S rRNA genes (total 903 bp) in a reduced set of taxa corroborated the monophyly of the lineage containing these three genera and identified the Asian genus Fejervarya as its possible sister group. The fact that the African H. occipitalis is nested within an otherwise exclusively Asian clade indicates its probable Oriental origin. Rough molecular clock estimates did not contradict the assumption that the dispersal event took place in the Miocene. Our data further identified a similar molecular divergence between closely related Asian and African species of Rana (belonging to the section Hylarana), indicating that Neogene intercontinental dispersal also may have taken place in this group and possibly in rhacophorid treefrogs.     

Incongruence in the pattern and timing of intra-specific diversification in bronze frogs and bullfrogs (Ranidae)

We compare patterns of lineage divergence in mitochondrial DNA (mtDNA) sequences of two protein-encoding mitochondrial genes (cyt b and ND2) in two ecologically similar, co-distributed, and closely related ranid frogs (Rana clamitans and Rana catesbeiana), that are geographically widespread, and frequently syntopic. We identified three lineages in R. clamitans, separated by 0.5% to 2.1% net corrected sequence divergence, comparable to two R. catesbeiana lineages separated by 0.6%. The geographic pattern of lineage distribution differed notably between the two species. In R. clamitans, we found a Coastal Plain-Appalachian (CPA) lineage restricted to south and east of the Appalachian Mountains and a widespread lineage that encompassing nearly all the sampled range. A third distinct and divergent lineage was detected in one location in the southwest portion of the range (Louisiana). This pattern contrasts with the east-west pattern in R. catesbeiana, and reflects possible differences in refugial dynamics and patterns of range expansion. Although both species have undergone range expansion and population growth, coalescent reconstruction of N(e) reflects larger lineages but more recent divergence in R. clamitans relative to R. catesbeiana, reflecting significant differences in population history or divergent patterns of molecular evolution at mtDNA.