The phylogenetic position of Streptococcus and Enterococcus

Streptococcus pyogenes, S. equinus, S. bovis, S. salivarius, S. sanguis, S. mutans, S. rattus, S. cricetus, S. lactis, S. raffinolactis and Enterococcus faecalis have been characterized by oligonucleotide cataloguing of their 16S ribosomal RNA. All the organisms form a loose but coherent group that is phylogenetically equivalent to those of lactobacilli, bacilli, the Brochothrix and Listeria group, and related taxa that constitute one of several sublines within the 'Clostridium' branch of Gram-positive eubacteria. Within the Steptococcus-Enterococcus group, organisms fall into three moderately related clusters defined by Enterococcus, the lactic acid streptococci and streptococci of the pyogenic and oral groups, respectively.     

水生植物排水草科的系统学位置

长期以来,小型水生植物类群排水草科（Hydate Uaceae）一直被认为是单子叶植物。最近的分子系统学研究表明,该科应隶属于基部被子植物（Basal Angiosperm）,和睡莲类植物为姐妹群。分类学家对该类群进行了系统修订,合并了该科的2个属,现有1属12种植物。对该科的深入研究正引起生物学家的广泛兴趣：     

The phylogenetic position of the Prolecithophora (Rhabditophora, 'Platyhelminthes')

Complete 18S ribosomal DNA (rDNA) sequences and partial 28S rDNA sequences from a selection of rhabditophoran taxa were obtained and used in combination with literature data to determine the phylogenetic position of the Prolecithophora and of two families sometimes included in the Prolecithophora, the Urastomidae and the Genostomatidae. The results are largely compatible with earlier molecular studies when supported clades are considered, and adjusting for the denser taxonomic sampling of this study. The position of the Proseriata is not compatible with the taxon Seriata, which is rejected. The Rhabdocoela excluding the Fecampiida and the Neodermata is monophyletic. The phylogenetic position of the Neodermata cannot be determined, but its placement is not compatible with the proposed taxa Revertospermata and Mediofusata Kornakova & Joffe, 1999, which are rejected. The Urastomidae and the Genostomatidae in all analyses group with the Fecampiida, and it is our recommendation that these taxa be included in the Fecampiida. The amended Fecampiida always group separately from the Prolecithophora sensu stricto , the Rhabdocoela, and the Neodermata. Our analyses reveal the existence of a strongly supported clade consisting of Prolecithophora + Tricladida + the amended Fecampiida, and we propose the name Adiaphanida for this clade. Tentatively the sister group of the Prolecithophora is a clade consisting of the Tricladida + amended Fecampiida.     

The phylogenetic position of Aulotandra (Zingiberaceae)

The phylogenetic position ofAulotandra (Zingiberaceae).—Nord. J. Bot. 23 : 725–734. Copenhagen. ISSN 0107–055X.
Molecular data for 41 representatives of Zingiberaceae are analysed focusing on the phylogenetic position of Aulotandra and its relationship to Siphonochilus. Sequence divergences indicate that accessions of Aulotandra from Madagascar are closest to those of African Siphonochilus in both ITS and trnL-F data sets, indicating a close relationship. Together these genera form a highly supported monophyletic clade. This African-Madagascan lineage is sister to the rest of the family with African, Asian and South American members, showing that Aulotandra does not belong in the tribe Alpinieae, where it has been traditionally placed, but in the subfamily Siphonochiloideae with the genus Siphonochilus.     

Lanzia berggrenii及其相关种的系统发育地位(英文)

系统发育分析结果表明,尽管Lanzia berggrenii能在寄主中形成基物子座,但与膜盘菌属的核心种关系较近,而与蜡盘菌科成员关系较远,应该归属于膜盘菌属。在广义的膜盘菌属的系统树中该种及在新西兰发现的4个新种构成一个单系群,分别命名为Hymenoscyphus haasticus,H. kiko,H.ohakune和H.waikaia。它们的共同特征:基物均为南青冈叶片,侧丝顶端分枝形成类似囊层被的结构,覆盖于子实层上部。Lanzia berggrenii var.metrosideri应为膜盘菌属中一个独立的种,即Hymenoscyphus metrosideri。     

The phylogenetic position of the Pterosauria within the Archosauromorpha

In recent years the hypothesis that pterosaurs were the major sister-group of dinosaurs and a closely-linked hypothesis that pterosaurs evolved flight from the ground up have gained general acceptance. A cladistic analysis of the Archosauromorpha using characters presented by previous workers results in a single most parsimonious tree with the Pterosauria as the major sister-group of the Dinosauria. However, that sister-group relationship is supported only by a suite of hindlimb characters that are correlated with bipedal digitigrade locomotion in dinosaurs. In pterosaurs the characters have been interpreted as correlates of bipedal cursorial locomotion, arboreal leaping, or involvement of the hindlimb in the wing. The homology of those characters in dinosaurs and pterosaurs cannot be supported. Reanalysis of the data after exclusion of those hindlimb characters results in most parsimonious trees with the Pterosauria as the sister-group of the Erythrosuchidae + Proterochampsidae + Euparkeria + Archosauria, in that order. This sister-group relationship is supported by a diverse assemblage of functionally independent skeletal characters from all regions of the skeleton. The results of the analysis cast doubt on the hypothesis that pterosaurs evolved flight from the ground up.     

The position of the Arthropoda in the phylogenetic system

Traditionally, Panarthropoda (Euarthropoda, Onychophora, Tardigrada) are regarded as being closely related to Annelida in a taxon Articulata, but this is not supported by molecular analyses. Comparisons of gene sequences suggest that all molting taxa (Panarthropoda, Nematoda, Nematomorpha, Priapulida, Kinorhyncha, Loricifera) are related in a monophyletic taxon Ecdysozoa. An examination of the characters supporting Articulata reveals that only segmentation with a teloblastic segment formation and the existence of segmental coelomic cavities with nephridia support the Articulata, whereas all other characters are modified or reduced in the panarthropod lineage. Another set of characters is presented that supports the monophyly of Ecdysozoa: molting under influence of ecdysteroid hormones, loss of locomotory cilia, trilayered cuticle and the formation of the epicuticle from the tips of epidermal microvilli. Comparative morphology suggests Gastrotricha as the sister group of Ecdysozoa with the synapomorphies: triradiate muscular sucking pharynx and terminal mouth opening. Thus there are morphological characters that support Articulata, but molecular as well as morphological data advocate Ecdysozoa. Comparison of both hypotheses should prompt further thorough and targeted investigations. J. Morphol. 238:263–285, 1998. © 1998 Wiley-Liss, Inc.     

The life and death of torquirhynchia inconstans (brachiopoda,upper jurassic) in England

Torquirhynchia inconstans, a rhynchonellid brachiopod, shows a curious asymmetric commissure. This is interpreted as an adaptation to life in tidal environments. Type of preservation, growth line, and size frequency analysis indicate that the population analyzed consist of dominantly mature individuals, which by analogy with recent brachiopod populations is a primary feature of the original population, and not due to selective destruction, selective transport, or selective predation of smaller individuals. The possible functions of the asymmetry of Torquirhynchia inconstans are considered, and it is concluded that the brachiopod was adapted to life in tidal environments, a conclusion supported by sedimentological evidence. Asymmetric brachiopods are considered to have developed from colonies of partly asymmetric, variable brachiopods by selection of extreme variants.     

Conflicting phylogenetic position of Schizosaccharomyces pombe

The phylogenetic position of the fission yeast Schizosaccharomyces pombe in the fungal Tree of Life is still controversial. Three alternative phylogenetic positions have been proposed in the literature, namely (1) a position basal to the Hemiascomycetes and Euascomycetes, (2) a position as a sister group to the Euascomycetes with the Hemiascomycetes as a basal branch, or (3) a sister group to the Hemiascomycetes with Euascomycetes as a basal branch. Here we compared 91 clusters of orthologous proteins containing a single orthologue that are shared by 19 eukaryote genomes. The major part of these 91 orthologues supports a phylogenetic position of S. pombe as a basal lineage among the Ascomycota, thus supporting the second proposition. Interestingly, part of the orthologous proteins supported a fourth, not yet described alternative, in which S. pombe is basal to both Basidiomycota and Ascomycota. Both topologies of phylogenetic trees are well supported. We believe that both reflect correctly the phylogenetic history of the species concerned. This apparent paradox may point to a heterogeneous nuclear genome of the fungi. Importantly, this needs to be taken in consideration for a correct understanding of the fungal Tree of Life.     

Structure and occurrence of cyphonautes larvae (bryozoa,ectoprocta)

We have studied larvae of the freshwater ctenostome Hislopia malayensis with scanning electron microscopy (SEM), confocal laser scanning microscopy (CLSM), and LM of serial sections. Some additional observations on larvae of M. membranacea using SEM and CLSM are also reported. The overall configuration of muscles, nerves, and cilia of the two larvae are identical. However, the larva of H. malayensis is much smaller than that of M. membranacea, which may explain most of the differences observed. Although all major nerves and muscle strands are present in H. malayensis, they are generally composed of fewer fibers. The H. malayensis larva lacks the anterior and posterior intervalve cilia. Its pyriform organ is unciliated with only a small central depression. The adhesive epithelium is not invaginated as an adhesive sac and lacks the large muscles interpreted as adhesive sac muscles in the M. membranacea larva. The velum carries two rows of ciliated cells, though the lower “row” consists of only one or two cells. Both rows of ciliated cells are innervated by nerves, which have not been detected in the M. membranacea larva. The ciliated ridge of H. malayensis lacks the frontal cilia. The planktotrophic cyphonautes larvae in a number of ctenostome clades and in the “basal” cheilostome clade Malacostega (and probably in the earliest cheilostomes) support the idea that the cyphonautes larva is the ancestral larval type of the Eurystomata. It may even represent the ancestral larval type of the bryozoans (= ectoprocts). J. Morphol. 271:1094‐1109, 2010. © 2010 Wiley‐Liss, Inc.     

Ecology,conservation, and phylogenetic position of the Madagascar Jacana Actophilornis albinucha

The Madagascar Jacana Actophilornis albinucha (Jacanidae) is an endemic shorebird found in the threatened wetlands of western Madagascar. This species is presumed to exhibit classical polyandry; however, few data are available to support that assumption. More generally, a lack of basic understanding of this species hinders conservation efforts. We conducted the most extensive study of the Madagascar Jacana to date, and report on its: 1) distribution, population size and density; 2) degree of sexual size dimorphism; and 3) phylogenetic position. The surveys were conducted at 54 lakes, between January and October in 2016. Madagascar Jacana were found at 22 lakes, and within these were distributed at a mean density of 3.5 ± 0.74 [SE] individuals per hectare of surveyed habitat. We estimate the global population size to be between 975 and 2 064 individuals, and habitat destruction appears to be the main threat to the species. Females were significantly larger than males, consistent with reports for other Jacanidae species. Using a mitochondrial DNA fragment, we expanded the Jacanidae genetic phylogeny, and confirmed that Madagascar Jacana is the sister species to the African Jacana Actophilornis africanus. Further studies are urgently needed to thoroughly re-assess the threat status and population trend of the Madagascar Jacana.     

The phylogenetic position of the Pterosauria within the Archosauromorpha re-examined

A previous analysis of the phylogenetic position of the Pterosauria argued that pterosaurs were not closely related to dinosaurs as is generally accepted, but rather were outside the crown group Archosauria. However, that study was dismissed for the use of inappropriate methods. Here, the data set from that analysis was divided into five partitions: one with characters associated with cursorial digitigrade bipedal locomotion and the other four with characters from the skull and mandible, postcranial axial skeleton, forelimb and hindlimb, respectively. The partitions were subjected to homogeneity testing, and the Cursorial partition was found to be incongruent with other partitions and all other characters at the α = 0.01 probability level. Deletion of the Pterosauria removed all significant incongruence, demonstrating that the incongruence results from the coding of pterosaurs for the cursorial characters. The cause of the incongruence was interpreted as homoplasy in hindlimb morphology, and after re-evaluating and reformulating the characters of the Cursorial partition, the revised data set was tested for homogeneity and no significant incongruence was found. Lastly, the data set was updated with additional characters and taxa from recent analyses, tested as before, and when analysed suggested that the Pterosauria were basal archosauriforms well outside the crown group Archosauria.     

The phylogenetic position of the Galápagos Cormorant

The endangered Galápagos Cormorant, Phalacrocorax harrisi, is unique among the species of the Phalacrocoracidae in being flightless and sequentially polyandrous. It has had a vexed taxonomic history, variously being lumped with all the species in Phalacrocorax, being accorded its own genus, Nannopterum, or being included in Leucocarbo or Compsohalieus. Different authorities have similarly suggested a number of different species as being its closest relative. Here we use novel mitochondrial DNA sequence data to show that the Galápagos Cormorant is related to the sister pair of the mainland Americas, the Double-crested Cormorant, P. auritus, and the Neotropic Cormorant, P. brasilianus. This trio of species has high statistical support (Bayesian posterior probability of 1.00; NJ bootstrap 98%; MP bootstrap 91%). The Galápagos Cormorant is thus a relatively recent offshoot of the mainland form, which has subsequently evolved flightlessness. Until the phylogeny of the cormorants is more clearly resolved, we recommend the continued use of Phalacrocorax for all species.     

The phylogenetic position of the world's smallest passerine,the Pygmy Bushtit Psaltria exilis

The Pygmy Bushtit is confined to the montane forests of Java. It is the world's smallest passerine and morphologically resembles a small, drab long‐tailed tit or bushtit (Aegithalidae). In its behaviour the Pygmy Bushtit show similarities with the members of the Aegithalidae, but owing to its small size and isolated geographical distribution relative to the other members of the Aegithalidae, it has always been placed in a monotypic genus within the family. The affinities of the Pygmy Bushtit have never been tested in a phylogenetic context and the species has to date not been included in any molecular studies. In this study we use sequence data from four different genetic markers to place it in the passerine phylogenetic tree. Our results confirm the inclusion of the Pygmy Bushtit in the Aegithalidae, but rather than being an isolated lineage, our results strongly suggest that it is nested in the Aegithalos clade, and most closely related to the Black‐throated Bushtit Aegithalos concinnus. The range of the Black‐throated Bushtit extends south into subtropical Indochina, with an isolated subspecies occurring in southern Vietnam. The Black‐throated Bushtit contains several morphologically and genetically distinct lineages, which could represent distinct species, but the phylogenetic relationships within this complex are poorly resolved and partly in conflict with current taxonomic treatment based on morphology.     

On the phylogenetic position of monotremes (Mammalia,Monotremata)

Henosferida from the Middle-Upper Jurassic of Western Gondwana is the most probable sister group for monotremes. They share the derived pretribosphenic structure of lower molars combined with the presumably absent protocone on the upper molars and the plesiomorphic retention of postdentary bones and pseudangular process of the lower jaw. In addition, the two groups share the dental formula with three molars and the position of the Meckel’s groove, which passes ventral to the mandibular foramen. In the course of subsequent evolution, monotremes acquired the mammalian middle ear with three auditory ossicles independently of therian mammals and multituberculates. Jurassic Laurasian Shuotheriidae are probably a sister group of the Gondwanian clade Henosferida + Monotremata. The Jurassic shuotheriid Pseudotribos shows a great plesiomorphic similarity to monotremes in the structure of the pectoral girdle, with a large interclavicle immovably connected to the clavicle. In the lineages leading to therian mammals and multituberculates, the pectoral girdle changed probably independently and in parallel in connection with the establishment of the parasagittal posture of the forelimbs (reduction of the interclavicle, mobile articulation of the interclavicle with clavicle, reduction of the procoracoid, and development of a supraspinous fossa of the scapula) and formation of the mammalian middle ear with three auditory ossicles.     

The phylogenetic position of the oxymonad Saccinobaculus based on SSU rRNA

The oxymonads are a group of structurally complex anaerobic flagellates about which we know very little. They are found in association with complex microbial communities in the guts of animals. There are five recognized families of oxymonads; molecular data have been acquired for four of these. Here, we describe the first molecular data from the last remaining group, represented by Saccinobaculus, an organism that is found exclusively in the hindgut of the wood-eating cockroach Cryptocercus. We sequenced small subunit ribosomal RNA (SSU rRNA) from total gut DNA to describe Saccinobaculus SSU rRNA diversity. We also sequenced SSU rRNA from manually isolated cells of the two most abundant and readily identifiable species: the type species Saccinobaculus ambloaxostylus and the taxonomically contentious Saccinobaculus doroaxostylus. We inferred phylogenetic trees including all five known oxymonad subgroups in order to elucidate the internal phylogeny of this poorly studied group, to resolve some outstanding issues of the taxonomy and identification of certain Saccinobaculus species, and to investigate the evolution of character states within it. Our analysis recovered strong support for the existence of the five subgroups of oxymonads, and consistently united the subgroups containing Monocercomonoides and Streblomastix, but was unable to resolve any further higher-order branching patterns.     

The phylogenetic position of taxaceae based on 18S rRNA sequences

The evolutionary position of the yew family, Taxaceae, has been very controversial. Some plant taxonomists strongly advocate excluding Taxaceae from the conifer order and raising its taxonomic status to a new order or even class because of its absence of seed cones, contrary to the case in the majority of conifers. However, other authors believe that the Taxaceae are not fundamentally different from the rest of the conifers except in that they possess the most reduced solitary-ovule cones. To resolve the controversy, we have sequenced the 18S rRNA genes from representative gymnosperms: Taxus mairei (Taxaceae), Podocarpus nakaii (Podocarpaceae), Pinus luchuensis (Pinaceae), and Ginkgo biloba (Ginkgoales). Our phylogenetic analysis of the new sequence data with the published 18S rRNA sequence of Zamia pumila (a cycad) as an outgroup strongly indicates that Taxus, Pinus, and Podocarpus form a monophyletic group with the exclusion of Ginkgo and that Taxus is more closely related to Pinus than to Podocarpus. Therefore, Taxaceae should be classified as a family of Coniferales. Our finding that Taxaceae, Pinaceae, and Podocarpaceae form a clade contradicts both the view that the uniovulate seed of Taxaceae is a primitive character and the view that the Taxaceae are descendants of the Podocarpaceae. Rather, the uniovulate seed of Taxaceae and that of some species of Podocarpus appear to have different origins, probably all reduced from multiovulate cones. Correspondence to: W.-H. Li