基于16S rRNA序列的角蟾科部分属间系统关系

采用最大似然法(ML法)、最大简约法(MP法)、邻接法(NJ法)对来自角蟾科Megophryidae(Anura)8属17种及外群2种共25条400bp左右的线粒体16S rRNA序列进行系统发育关系分析。结果表明,用于分析的所有角蟾科物种形成两大支,第一支包括Megophrys,Brachytarsophrys和Atympanophrys,第二支包括Leptobrachium,Leptolalax,Scutiger,Oreolalax和Vibrissaphora。支持将角蟾科划分为两大类群,即第一支属于Megophryini族．第二支属于Leptobrachiini族。根据分子钟模型初步推测两类群问的分歧时间大致为14．2～18．7百万年前。在Megophryini族中,基因树的拓扑结构不支持Atympanophrys建立后的Megophrys为单系;而在Leptobrachiini族中,Leptolalax为一有效属,其系统发生较早。     

基于线粒体12S和16S rRNA基因部分序列的角蟾亚科部分属种的系统发育关系

测定了角蟾亚科2属8种(亚种)和外群3种的线粒体12S和16S rRNA基因部分DNA序列,比对后序列长共949bp,其中变异位点数320,简约位点数206。邻接法和最大简约法分析的系统关系树一致表明内群为一单系群,其中腺角蟾首先与其他物种分开;沙坪角蟾与宽头短腿蟾聚为一支;余下的5种(亚种)角蟾组成一支,其中小角蟾短肢亚种的广西种群和香港种群聚为一亚支,另一亚支包括峨眉角蟾、小角蟾指名亚种、尾凸角蟾和重庆武隆的角蟾种,后两种角蟾进化关系最近。本结果支持短肢角蟾为有效种,同时提示腺角蟾、沙坪角蟾与宽头短腿蟾可能隶属3个不同的亚属或属。     

丝瓜藓属(Pohlia Hedw.)的系统位置及属内种间关系探讨

丝瓜藓属的系统地位及属内种间关系存在争议。本研究首次利用核糖体DNA内转录间区(ITS)序列数据对丝瓜藓属及相关科属植物进行系统发育分析。最大简约法,最大似然法及贝叶斯推论法构建的系统树均表明,ITS序列数据不支持将丝瓜藓属划归提灯藓科。丝瓜藓属植物与缺齿藓属植物构成一个单系分支。Brotherus(1903),Ochi(1959),Shaw(1984)及Hill等(2006)等学者提出的丝瓜藓属属下分类均不是单系类群。     

基于叶绿体rps16基因和核基因ITS片段研究肉苁蓉属系统位置

在前人对列当科系统发育研究的基础上,追加了肉苁蓉属(Cistanche)的基因序列数据,运用最大简约法、最大似然法和贝叶斯推断方法探讨了其在列当科中的系统位置及列当科中属间关系.基于rps16基因序列及rps16+ ITS联合序列建立了列当科系统发育树,结果显示,肉苁蓉属、列当属(Orobanche)以及草苁蓉属(Boschniakia)聚在同一进化枝内,肉苁蓉属和列当属表现出最近亲缘关系;列当科中的全寄生类群、半寄生类群和非寄生类群分属在3个不同分支中.     

中国熊野藻属植物系统发育分析——基于叶绿体UPA序列

以中国产的6种熊野藻属(Kumanoa)和串珠藻属(Batrachospermum)植物为材料,测定其UPA序列,并在GenBank中下载相关基因序列,通过贝叶斯法、最大似然法和邻接法构建系统发育树,分析其系统发育。结果显示,UPA序列核苷酸变异位点占序列长度的43.1%,其中简约信息位点占序列长度的31.1%,种间差异度为0~1.81%,属间差异度大于4.19%,可以作为分子标记用于系统发育分析。中国产熊野藻属的两个种和来自世界范围内的多数该属种类聚为一大支,支持该属的建立。基于UPA序列的地理起源分析显示,两属的祖先分布区节点主要在北美洲和大洋洲,然后向其它地区扩散,熊野藻属向外扩散后,在南美洲分布较为集中。     

基于ITS序列分析仲彬草属植物的亲缘关系

以旱雀麦为外类群,用PAUP 4.0b10软件并采用最大简约法和邻接法对11份仲彬草属物种的ITS区序列进行系统发育分析,两种方法得到的系统发育树基本一致。结果表明:(1)整个ITS序列长度变异范围为596~601 bp;G C含量在所有ITS中的变化范围为61.20%~62.44%;序列间的遗传分化距离为0.003~0.033,平均值为0.015;(2)疏花仲彬草和塔克拉干仲彬草2个物种聚为一支,位于系统发育树的底部,在最大简约法和邻接法分析中分别获得78%和82%的自展支持率,它们之间的亲缘关系较近;(3)形态相似、地理分布一致的物种有聚在一起的倾向,表现出较近的亲缘关系;(4)ITS区序列分析的结果与细胞学、形态学的研究结果基本一致,因此ITS区序列分析能反映仲彬草属种间关系。     

基于叶绿体rps16基因和核基因ITS片段研究肉苁蓉属系统位置

在前人对列当科系统发育研究的基础上,追加了肉苁蓉属(Cistanche)的基因序列数据,运用最大简约法、最大似然法和贝叶斯推断方法探讨了其在列当科中的系统位置及列当科中属间关系。基于rps16基因序列及rps16+ITS联合序列建立了列当科系统发育树,结果显示,肉苁蓉属、列当属(Orobanche)以及草苁蓉属(Boschniakia)聚在同一进化枝内,肉苁蓉属和列当属表现出最近亲缘关系;列当科中的全寄生类群、半寄生类群和非寄生类群分属在3个不同分支中。     

重庆黔江发现尾突角蟾

2022年7月在重庆市黔江区武陵山市级自然保护区采集到1号两栖动物标本,经形态特征比较,与尾突角蟾（Boulenophrys caudoprocta）相似;基于线粒体16Sr RNA和COI基因联合构建布角蟾属（Boulenophrys）部分物种系统发育树,此次采集的角蟾标本与尾突角蟾聚为一支,具有较高的支持率（1/100,贝叶斯法/最大似然超快速引导支持分析值）;基于p-distance估算本次采集的角蟾标本与尾突角蟾湖南模式产地标本间的遗传距离为0%,远小于角蟾属物种间的遗传距离（8.7%～15.9%）。综合形态特征和分子系统发育比较,确定此次采集到的角蟾标本为无尾目（Anura）角蟾科（Megophryidae）布角蟾属的尾突角蟾,系重庆市两栖动物分布新记录种。重庆市尾突角蟾的发现,进一步扩展了该地区的物种名录,拓宽了对尾突角蟾分布范围的认知,为该属区系分类学和系统学提供了新信息,同时为当地生态系统和物种多样性的研究提供了基础信息,对制定更加全面和针对性的保护措施有着积极的促进作用。     

基于线粒体和核基因序列的蜜蜂属系统发育分析

文章测定了中国分布的蜜蜂属(Apis)5种蜜蜂22个样本的线粒体基因ND2、CO2、16S rRNA以及核基因ITPR的序列,对序列的碱基组成和蜜蜂种间的遗传距离进行了分析。结合下载的蜜蜂属其他4个种的相关序列,采用最大简约法、邻接法和最大似然法重建了蜜蜂属系统发育关系。系统发育分析结果支持蜜蜂属划分为3个类群,即小蜜蜂类群(包括小蜜蜂和黑小蜜蜂)、大蜜蜂类群(包括大蜜蜂和黑大蜜蜂)和穴居蜜蜂类群(西方蜜蜂、东方蜜蜂、沙巴蜂、苏拉威西蜂、绿努蜂),且小蜜蜂类群较早分化。结果还显示,我国海南岛的大蜜蜂和大陆的大蜜蜂之间可能存在较大的遗传分歧。     

中国库蚊属四十个种(亚种)的分子系统发育关系研究(双翅目:蚊科)

【目的】对在中国有分布的库蚊属Culex种(亚种)的COⅠ序列和ITS2序列进行测序,构建和讨论这些种(亚种)的分子系统发育关系。【方法】测定了库蚊属20个种(亚种)的COⅠ和ITS2序列,并从NCBI数据库中下载了库蚊属另外20个种(亚种)的COⅠ和3个种(亚种)的ITS2序列。对库蚊属40个种(亚种)的COⅠ序列和其中23个种(亚种)的ITS2序列进行碱基构成、种间遗传距离和饱和度分析,并对COⅠ+ITS2序列进行ILD(incongruence length difference)检验。分别使用2种分子数据集(COⅠ和ITS2)的核苷酸序列,用最大似然法(ML)、贝叶斯法(BI)、邻接法(NJ)和最大简约法(MP)推断这些种的系统发育关系。通过Kishino-Hasegawa(KH)和ShimodairaHasegawa(SH)检验评估这4种系统树间的差异,确定最为合理的系统发育树。【结果】本研究新测序获得20种(亚种)的COⅠ和ITS2序列的长度范围分别为625~685 bp和300~559 bp。COⅠ和ITS2序列在库蚊属成对蚊种间的遗传距离分别是0.002~0.198和0.006~1.807。库蚊属23个种(亚种)的COⅠ+ITS2序列的ILD检验结果显示,数据集具有不相容性,因此COⅠ+ITS2序列不适用于这些种(亚种)的系统发育研究。经KH和SH检验显示,4种系统发育树中,基于COⅠ序列构建的BI树最为合理,而基于ITS2序列构建的MP树最为合理。基于COⅠ核苷酸序列所构建的BI树显示,除幼小库蚊Cx.infantulus和短须库蚊Cx.brevipalpis外,各亚属间成员聚类结果与传统的形态学归类结果吻合;路蚊亚属Lutiza和包蚊亚属Barraudius都归入库蚊亚属Culex内;梅蚊亚属Maillotia和新库蚊亚属Nexoculex聚为一支;库状蚊亚属Culiciomyia、真黑蚊亚属Eumelanomyia和簇角蚊亚属Lophoceramyia均显示为单系。基于ITS2序列所构建的MP树显示,各亚属间和种(亚种)间关系混乱。【结论】重建的分子系统发育树表明库蚊亚属不是一个单系群。在重建库蚊属系统发育关系时,相较于ITS2和COⅠ+ITS2,COⅠ是更为理想的分子标记。本研究构建的分子系统发育关系为中国库蚊属中各亚属和各种(亚种)之间的亲缘关系的研究奠定了基础。     

角蟾亚科3物种皮肤的组织学观察

应用石蜡切片和H.E染色技术,对角蟾亚科3个属的代表物种:短肢异角蟾(Xenophrys brachykolos)、宽头短腿蟾(Brachytarsophrys carinense)和小口拟角蟾(Ophryophryne microstoma)的皮肤进行了组织学观察及参数测量比较。分别取头背、体背和体腹3个部位的皮肤进行观察。结果表明,3物种的皮肤基本结构相似,均由表皮和真皮组成,真皮包括疏松层和致密层,疏松层中有大量腺体分布,包括黏液腺和颗粒腺2种。皮肤厚度、各组织层相对厚度以及腺体密度之间存在种间差异和部位差异。在宽头短腿蟾背部皮肤中,发现了与尖吻山角蟾(Megophrys nasuta)皮肤中一种片层状、H.E染色呈蓝色的皮肤真皮骨化结构(osteoderms)很相似的结构;短肢异角蟾皮肤中有明显的钙化层结构,小口拟角蟾皮肤钙化程度较弱。皮肤的骨化和钙化可能具有防止水分流失,抵御干燥的功能。2种内骨骼在角蟾亚科中同时存在,为探讨两栖动物皮肤内骨骼的进化提供了重要的研究基础。     

Nuclear and mitochondrial DNA evidence of polyphyly in the avian superfamily Muscicapoidea

Nucleotide sequences of the nuclear c-mos gene and the mitochondrial cytochrome b and ND2 genes were used to assess the monophyly of Sibley and Monroe's [Distribution and Taxonomy of Birds of the World, Yale University Press, New Haven, 1990] Muscicapoidea superfamily. The relationships and monophyly of major lineages within the superfamily, as well as genera membership in major lineages was also assessed. Analyses suggest that Bombycillidae is not a part of Muscicapoidea, and there is strongly supported evidence to suggest that Turdinae is not part of the Muscicapidae, but is instead sister to a Sturnidae+Cinclidae clade. This clade is in turn sister to Muscicapidae (Muscicapini+Saxicolini). Of the 49 Turdinae and Muscicapidae genera that we included in our analyses, 10 (20%) are shown to be misclassified to subfamily or tribe. Our results place one current Saxicolini genus in Turdinae, two Saxicolini genera in Muscicapini, and five Turdinae and two Muscicapini genera in Saxicolini; these relationships are supported with 100% Bayesian support. Our analyses suggest that c-mos was only marginally useful in resolving these "deep" phylogenetic relationships.     

Out of the blue: a novel, trans-Atlantic clade of geckos (Gekkota, Squamata)

Phylogenetic relationships among gekkotan lizards were estimated from five nuclear protein-coding genes in separate and combined analyses using maximum parsimony, maximum likelihood and Bayesian analyses. All analyses recovered a monophyletic trans-Atlantic gecko clade (Phyllodactylidae) consisting of the genera Asaccus, Haemodracon, Homonota, Phyllodactylus, Phyllopezus, Ptyodactylus, Tarentola and Thecadactylus . No other phylogenetic or taxonomic hypotheses have proposed linking these genera, which have been consistently grouped with other taxa outside of the clade. In this paper, we determine the relationships of this new clade to other major gekkotan groups, evaluate previous phylogenetic hypotheses regarding constituent members of this novel clade, and critically examine the use of historically important morphological characters in gekkotan systematics as they relate to this novel clade, specifically — phalangeal formulae, hyoid morphology and external structure of the toe-pads.     

Phylogenetic analyses of the genera Pipra, Lepidothrix and Dixiphia (Pipridae, Passeriformes) using partial cytochrome b and 16S mtDNA genes

The piprids (manakins) are small-bodied Neotropical birds characterized by sexual dimorphism of the plumage and elaborate courtship rituals. The phylogenetic relationships of some of piprid genera, in particular Pipra , are not well defined. Recently, Pipra was divided into three distinct groups, and the recognition of two new genera — Lepidothrix and Dixiphia — was suggested, based on the characteristic of the syringial morphology. In the present study, we analyse the phylogenetic relationships among these genera on the basis of data from the mitochondrial genes rRNA 16S and cytochrome b . Bayesian Inference (BI), Maximum Parsimony (MP) and Maximum Likelihood (ML) methods of analyses produced phylogenetic trees with very similar topologies with regard to the groupings formed by the species representing the three genera. These results indicate that the genera Pipra, Lepidothrix and Dixiphia do not constitute a single monophyletic clade, and support the current hypothesis of polyphyletism for the former representatives of the genus Pipra . However, the topologies presented do not coincide exactly with the phylogeny suggested by the morphological data with regard to the relationship between these three groups and the remaining piprid genera analysed here, emphasizing the need for further studies of this group of birds. The agreement between the molecular data presented here and the biogeographical information available for some of the species analysed appears to confirm the potential of using segments of the mitochondrial genome for the study of phylogeographical patterns in this group of organisms.     

Evidence for host-specific clades of tetraphyllidean tapeworms (Platyhelminthes: Eucestoda) revealed by analysis of 18S ssrDNA

Sequence data from the V4 and V7-V9 variable regions of the 18S small subunit ribosomal DNA (ssrDNA) gene were used to examine relationships among 26 tetraphyllidean and two lecanicephalidean taxa. Newly collected specimens of 21 of the tetraphyllidean species were used to generate ssrDNA sequences that were combined with sequences previously available, including those of two diphyllidean taxa used for outgroup rooting. The sequences were aligned by eye according to secondary structural motifs of the conserved core of the molecule. Of the 1520 sites in the alignment, 874 (58%) were excluded from analysis due to alignment gaps and lack of positional homology as inferred by manual inspection. Genetic variability of the ssrDNA gene regions compared was greater than would be expected, based on the present taxonomy of the ingroup species, and the genetic divergences among tetraphyllidean 'families' and genera were comparable to that among tapeworm orders. Phylogenetic hypotheses were generated by the methods of maximum parsimony and maximum likelihood (GTR + I + Gamma nucleotide substitution model). Four most parsimonious trees resulted from analysis by maximum parsimony. Strict consensus of the four trees supported the monophyly of the Tetraphyllidea, with the lecanicephalidean taxa forming a sister lineage. Among the tetraphyllidean taxa included in the analysis were three major clades: a basal clade including species of the phyllobothriid genera Anthocephalum, Echeneibothrium, Rhinebothrium, Rhodobothrium and Spongiobothrium; a clade uniting the phyllobothriids of the genus Duplicibothrium with the dioecotaeniid genus Dioecotaenia; and a larger sister clade to the Duplicibothrium + Dioecotaenia clade that included the phyllobothriid genera Caulohothrium, Ceratobothrium, Clistobothrium, Paraoryigmatobothrium and Prosobothrium, the litobothriid genus Litobothrium and the onchobothriid genera Acanthobothrium, Calliobothrium, Phoreiobothrium and Platybothrium. Maximum likelihood analysis resulted in a topology that was congruent where nodes were strongly supported by parsimony analysis, but differed in the relative positions of the well-supported clades. In addition,maximum likelihood analysis grouped the lecanicephalidean taxa among the tetraphyllidean taxa, indicating paraphyly of the order Tetraphyllidea as currently defined. Relationships suggested by both methods of analysis reflected common host associations of the taxa better than their current classification, suggesting that coevolution has had a significant role in the evolution of the group.     

Relationships of the temperate Australasian labrid fish tribe Odacini (Perciformes; Teleostei)

The labrid tribe Odacini comprises four genera and 12 species of fishes that inhabit shallow kelp forest and seagrass areas in temperate waters of Australia and New Zealand. Odacines are morphologically disparate, but share synapomorphies in fin structure and fusion of teeth into a beak-like oral jaw. A phylogenetic analysis of odacines was conducted to investigate their relationships to other labrid fishes, the relationships of species within the tribe, and the evolution of herbivory within the group. Fragments from two mitochondrial genes, 12S rDNA and 16S rDNA, and two nuclear genes, Tmo4C4 and RAG2, were sequenced for seven odacine species (representing all four genera), eight species representing the other major labrid lineages, and three outgroup species. Maximum likelihood and maximum parsimony analyses on the resulting 2338 bp of DNA sequence produced nearly identical topologies differing only in the placement of a clade containing the cheiline Cheilinus fasciatus and the scarine Cryptotomus roseus. The remaining clades received strong bootstrap support under maximum parsimony, and all clades in the maximum likelihood analysis received high bootstrap proportions and high posterior probabilities. The hypsigenyine labrid Choerodon anchorago formed the sister group to the odacines. Within the odacines, Odax cyanoallix+Odax pullus formed the sister to the remaining odacines, with Odax acroptilus, Odax cyanomelas, and Siphonognathus argyrophanes forming successively closer sister groups to the clade Haletta semifasciatus+Neoodax balteatus. Either herbivory evolved twice in the odacines, or herbivory evolved once with two reversions to carnivory. The latter hypothesis appears more likely in the light of odacine feeding biology.     

The phylogeny of Myxosporea (Myxozoa) based on small subunit ribosomal RNA gene analysis

The phylogeny of the Myxosporea was studied using the small-subunit ribosomal RNA gene sequences. Maximum parsimony and Bayesian inference were used to determine myxosporean phylogenetic relationships. The analysis included 120 myxosporean sequences retrieved from GenBank and 21 newly obtained sequences of myxosporeans representing nine genera. Members of the genera Palliatus and Auerbachia were sequenced for the first time. The phylogenetic analysis supported a split of myxosporeans into two main lineages separating most of freshwater species from marine ones as described by previous authors. In addition to the two main lineages, a third lineage consisting of three species was found (Sphaerospora truttae, Sphaerospora elegans and Leptotheca ranae) and additional exceptions to the marine/freshwater myxosporean split were recognised (Sphaeromyxa hellandi, Sphaeromyxa longa and Myxidium coryphaenoideum). All three myxosporean lineages were characterised by specific lengths of SSU rDNA sequences. The lineage of marine myxosporeans split into five well-defined clades. They consisted of species with a similar site of infection and spore morphology and were referred as the Parvicapsula clade, the Enteromyxum clade, the Ceratomyxa clade, the marine Myxidium clade and the Kudoa clade, respectively. The inner topology of the freshwater clade was more complex but the trend to branch according to site of infection was observed in this clade as well. Due to the number of sequences available, a histozoic (Myxobolus clade) predominated. Interestingly, five morphologically different species infecting urinary bladder clustered within the histozoic (Myxobolus) clade. The phylogenetic trees derived from this study differ in a number of respects from the current taxonomy of the myxosporeans, which suggests that several currently utilised characters may be homoplasious or that reliance on a single gene tree may not adequately reflect the phylogeny of the group.