Phylogenetic relationships of the Australian Leptophlebiidae (Ephemeroptera)

2005 ◽  
Vol 19 (6) ◽  
pp. 531 ◽  
Author(s):  
Faye Christidis

Phylogenetic relationships among the Australian Leptophlebiidae genera and selected genera from South America and New Zealand were investigated using a cladistic analysis of 43 morphological characters. The outcomes of this analysis were largely consistent with the higher-level relationships previously proposed by Pescador and Peters (1980). The monophyly of the Meridialaris lineage (comprising Austrophlebioides, Tillyardophlebia, Kirrara, ‘WT sp. 1’ and ‘WT sp. 2’ from Australia, Meridialaris from South America and Deleatidium and Atalophlebioides from New Zealand) was strongly supported, as was the monophyly of the Nousia lineage (Nyungara, Nousia and Koorrnonga). However, Australian genera assigned to the Hapsiphlebia lineage (Atalophlebia, Kalbaybaria, Ulmerophlebia, Jappa and Atalomicria) did not form a monophlyletic group. There was support for a sister-group relationship between the Dactylophlebia and Meridialaris lineages, and for the placement of Garinjuga (Penaphlebia lineage) as the sister-group to a large clade comprising genera of the Nousia, Dactylophlebia and Meridialaris lineages. The phylogenetic analysis provided some clarification of the affinities of Neboissophlebia, Bibulmena, Loamaggalangta and Kaninga. These genera appear to belong to lineages not recognised previously among the Gondwanan Leptophlebiidae.

2020 ◽  
Vol 96 (2) ◽  
pp. 455-498
Author(s):  
Kai Horst George

Uncovering the systematics of CopepodaHarpacticoida, the second-most abundant component of the meiobenthos after Nematoda, is of major importance for any further research dedicated especially to ecological and biogeographical approaches. Based on the evolution of the podogennontan first swimming leg, a new phylogenetic concept of the Ancorabolidae Sars and Cletodidae T. Scott sensu Por (Copepoda, Harpacticoida) is presented, using morphological characteristics. It confirms the polyphyletic status of the Ancorabolidae and its subfamily Ancorabolinae Sars and the paraphyletic status of the subfamily Laophontodinae Lang. Moreover, it clarifies the phylogenetic relationships of the so far assigned members of the family. An exhaustive phylogenetic analysis was undertaken using 150 morphological characters, resulting in the establishment of a now well-justified monophylum Ancorabolidae. In that context, the Ancorabolus-lineage sensu Conroy-Dalton and Huys is elevated to sub-family rank. Furthermore, the membership of Ancorabolina George in a rearranged monophylum Laophontodinae is confirmed. Conversely, the Ceratonotus-group sensu Conroy-Dalton is transferred from the hitherto Ancorabolinae to the Cletodidae. Within these, the Ceratonotus-group and its hypothesised sister-group Cletodes Brady are combined to form a monophyletic subfamily Cletodinae T. Scott, subfam. nov. Consequently, it was necessary to restructure the Ancorabolidae, Ancorabolinae and Laophontodinae and extend the Cletodidae to include the displacement and exclusion of certain taxa. Moreover, comparison of the Ancorabolidae, Cletodidae, Laophontoidea and other Podogennonta shows that the Ancorabolidae and Cletodidae form sister-groups in a monophylum Cletodoidea Bowman and Abele, which similarly has a sister-group-relationship with the Laophontoidea T. Scott. According to the present study, both taxa constitute a derived monophylum within the Podogennonta Lang.


1998 ◽  
Vol 19 (4) ◽  
pp. 385-405 ◽  
Author(s):  
Van Wallach ◽  
Rainer Günther

AbstractThe internal anatomy of Xenophidion is described and compared with that of members of other snake families. A suite of primitive characters eliminates Xenophidion as a possible member of the Caenophidia; only two characters could conceivably suggest a relationship to the Caenophidia and both are examples of losses and thus of low phylogenetic value in assessing relationships. However, among lower snakes a sister group relationship is demonstrated with the Tropidophiidae of the Neotropical region. Besides possessing nearly identical viscera and topographical arrangement thereof, Xenophidion shares several characters with the Tropidophiidae. A new family is created to contain the genus, the Xenophidiidae. The Xenophidiidae share one synapomorphy with both the Tropidophiidae and Bolyeriidae. Therefore, it is proposed that these three families be united in the superfamily Tropidophioidea. A phylogenetic analysis of 52 characters results in the following preferred hypothesis of relationships: (Boinae, (((Bolyeria, Casarea), (Xenophidion, ((Exiliboa, Ungaliophis), (Trachyboa, Tropidophis)))), Acrochordus)).


2011 ◽  
Vol 279 (1731) ◽  
pp. 1093-1099 ◽  
Author(s):  
Maria Heikkilä ◽  
Lauri Kaila ◽  
Marko Mutanen ◽  
Carlos Peña ◽  
Niklas Wahlberg

Although the taxonomy of the ca 18 000 species of butterflies and skippers is well known, the family-level relationships are still debated. Here, we present, to our knowledge, the most comprehensive phylogenetic analysis of the superfamilies Papilionoidea, Hesperioidea and Hedyloidea to date based on morphological and molecular data. We reconstructed their phylogenetic relationships using parsimony and Bayesian approaches. We estimated times and rates of diversification along lineages in order to reconstruct their evolutionary history. Our results suggest that the butterflies, as traditionally understood, are paraphyletic, with Papilionidae being the sister-group to Hesperioidea, Hedyloidea and all other butterflies. Hence, the families in the current three superfamilies should be placed in a single superfamily Papilionoidea. In addition, we find that Hedylidae is sister to Hesperiidae, and this novel relationship is supported by two morphological characters. The families diverged in the Early Cretaceous but diversified after the Cretaceous–Palaeogene event. The diversification of butterflies is characterized by a slow speciation rate in the lineage leading to Baronia brevicornis , a period of stasis by the skippers after divergence and a burst of diversification in the lineages leading to Nymphalidae, Riodinidae and Lycaenidae.


Author(s):  
Christopher J. Glasby ◽  
Patricia A. Hutchings ◽  
Kathryn Hall

A phylogenetic analysis of the polychaete clade Terebelliformia (Terebellida) was undertaken in order to test monophyly of families and subfamilies and to determine their affinities. Parsimony analyses of 41 terebelliform species with outgroup Owenia fusiformis and 46 morphological characters yielded 106–144 most parsimonious trees with length 250, consistency index=0·432, retention index=0·659 and rescaled consistency index=0·285. Monophyly was indicated for Alvinellidae, Ampharetidae, Terebellidae and Trichobranchidae and the terebellid subfamily Polycirrinae. Monophyly of Terebellidae is supported by the presence of a ridge-like tentacular membrane. Monophyly of Polycirrinae is supported by the loss of branchiae, trilobed upper lip, pinnate secondary notochaetae and ventro-lateral pads. Recognition of Polycirrinae renders taxa in the other terebellid subfamilies—Terebellinae and Thelepodinae—paraphyletic. Our results do not support previous classifications that placed Trichobranchidae as a subfamily of Terebellidae; rather it should be considered equal in rank with Alvinellidae, Ampharetidae, Terebellidae and Pectinariidae. The following relationships were obtained: (Trichobranchidae ((Alvinellidae, Ampharetidae) (Pectinariidae, Terebellidae))). This is the first time a Pectinariidae–Terebellidae sister group relationship has been found; it is supported by the synapomorphic presence of ventral glandular shields.


2002 ◽  
Vol 16 (6) ◽  
pp. 957 ◽  
Author(s):  
J. T. Jennings ◽  
A. D. Austin

This study examines the phylogeny, taxonomy, distribution and biology of the gasteruptiid subfamily Hyptiogastrinae and, at the same time, presents an overview of the family. Following a cladistic analysis of 35 discrete morphological characters, two monophyletic genera are recognised, Hyptiogaster Kieffer and Pseudofoenus s. l. Kieffer. As a consequence, the genera Aulacofoenus Kieffer, Crassifoenus Crosskey, and Eufoenus Szépligeti are synonymised with Pseudofoenus. A total of 88 species are recognised for the subfamily, 10 species of Hyptiogaster, which are restricted to mainland Australia, and 78 species of Pseudofoenus, 40 of which are described as new. Pseudofoenus has a restricted Gondwanan distribution and is found in Australia including Tasmania (65 spp.), New Guinea and New Britain (5 spp.), the south-west Pacific (New Caledonia, New Hebrides and Fiji – 2 spp.), New Zealand (4 spp.) and South America (2 spp.). No new species have been recorded from either New Zealand or South America. For Pseudofoenus, information on the distribution of each species, their biology (if known) and an identification key are presented.Following a taxonomic revision, the following new species are described: P. baileyi, sp. nov., P. baitetaensis, sp. nov., P. beverlyae, sp. nov., P. caperatus, sp. nov., P. cardaleae, sp. nov., P. carrabinensis, sp. nov., P. claireae, sp. nov., P. collessi, sp. nov., P. coorowensis, sp. nov., P. crosskeyi, sp. nov., P. douglasorum, sp. nov., P. eliseae, sp. nov., P. ericae, sp. nov., P. eustonensis, sp. nov., P. feckneri, sp. nov., P. gressitti, sp. nov., P. gullanae, sp. nov., P. hackeri, sp. nov., P. imbricatus, sp. nov., P. iqbali, sp. nov., P. kadowi, sp. nov., P. karimuiensis, sp. nov., P. kelleri, sp. nov., P. leinsterensis, sp. nov., P. macdonaldi, sp. nov., P. malkini, sp. nov., P. marshalli, sp. nov., P. masneri, sp. nov., P. mitchellae, sp. nov., P. morganensis, sp. nov., P. nalbarraensis, sp. nov., P. pumilis, sp. nov., P. schmidti, sp. nov., P. stevensi, sp. nov., P. tasmaniensis, sp. nov., P. taylori, sp. nov., P. umboiensis, sp. nov., P. walkeri, sp. nov. and P. zborowskii, sp. nov. The synonymy of Aulacofoenus, Crassifoenus and Eufoenus with Pseudofoenus result in the following new combinations: from Aulacofoenus: P. bungeyi (Jennings & Austin), comb. nov., P. deletangi (Schletterer), comb. nov., P. fallax (Schletterer), comb. nov., P. fletcheri (Jennings & Austin), comb. nov., P. goonooensis (Jennings & Austin), comb. nov., P. infumatus (Schletterer), comb. nov., P. kurmondi (Jennings & Austin), comb. nov., P. loxleyi (Jennings & Austin), comb. nov., P. marionae (Jennings & Austin), comb. nov., P. perenjorii (Jennings & Austin), comb. nov., P. swani (Jennings & Austin), comb. nov., P. thoracicus (Guérin Menéville), comb. nov., P. whiani (Jennings & Austin), comb. nov. and P. wubinensis (Jennings & Austin), comb. nov.; from Crassifoenus: P. houstoni (Jennings & Austin), comb. nov., P. grossitarsis (Kieffer), comb. nov and P. macronyx (Schletterer), comb. nov.; and from Eufoenus: P. antennalis (Schletterer), comb. nov., P. australis (Westwood), comb. nov., P. crassitarsis (Kieffer), comb. nov., P. darwini (Westwood), comb. nov., P. extraneus (Turner), comb. nov., P. ferrugineus (Crosskey), comb. nov., P. floricolus (Turner), comb. nov., P. inaequalis (Turner), comb. nov., P. melanopleurus (Crosskey), comb. nov., P. minimus (Turner), comb. nov., P. nitidiusculus (Turner), comb. nov., P. patellatus (Westwood), comb. nov., P. pilosus (Kieffer), comb. nov., P. reticulatus (Crosskey), comb. nov., P. rieki (Crosskey), comb. nov., P. ritae (Cheesman), comb. nov. and P. spinitarsis (Westwood), comb. nov. Pseudofoenus microcephalus (Crosskey), comb. nov. is transferred from Hyptiogaster and Eufoenus flavinervis (Kieffer) remains incertae sedis.


Zootaxa ◽  
2006 ◽  
Vol 1302 (1) ◽  
pp. 43 ◽  
Author(s):  
EIRIK RINDAL ◽  
GEIR E.E. SØLI

A phylogenetic analysis of the Mycetophilinae is presented and discussed. The analysis is based on morphological characters for 27 genera. Fourteen equally parsimonious trees were found. The monophyly of the Mycetophilinae and the two tribes, Exechiini and Mycetophilini, is well supported. Within the Exechiini, good support for the sister-group relationship of Exechia and Exechiopsis was found, as was support for the inclusion of Cordyla in the tribe. The analysis provides good resolution within the Mycetophilini, with Trichonta as the sister group of the remaining taxa.


1997 ◽  
Vol 75 (6) ◽  
pp. 963-970 ◽  
Author(s):  
André-Denis G. Wright ◽  
Denis H. Lynn

Phylogenetic relationships within the largest family of entodiniomorphid rumen ciliates, the Ophryoscolecidae, were inferred from comparisons of small-subunit ribosomal RNA gene sequences. These included three new sequences from Diplodinium dentatum (1638 base pairs (bp)), Eudiplodinium maggii (1637 bp), and Ophryoscolex purkynjei (1636 bp). Using morphological characters, Lubinsky constructed a cladogram of the Ophryoscolecidae, and on the basis of his analysis, he divided the family into three subfamilies (Entodiniinae, Diplodiniinae, Ophryoscolecinae) to reflect his "natural" groupings (G. Lubinsky. 1957. Can. J. Zool. 35: 141 – 159). Our cladistic analysis, based on the limited morphological and ultrastructural data available, indicates that there are no synapomorphies supporting the Diplodiniinae sensu Lubinsky. However, based upon the six 18S sequences for the Ophryoscolecidae, the rumen ciliates are monophyletic and fall into three distinct groups corresponding to Lubinsky's subfamilial division of the family. Our molecular analysis shows Entodinium to be the earliest branching rumen ciliate (subfamily Entodiniinae) and Eudiplodinium, not Diplodiium, branching first among the diplodiniines.


2010 ◽  
Vol 24 (5) ◽  
pp. 473 ◽  
Author(s):  
Christiane Weirauch ◽  
Randall T. Schuh

Transantarctic distributional patterns are common in many groups of insects and plants including Coleorrhyncha, the sister group of Heteroptera. In contrast, evidence for such patterns within Heteroptera, or true bugs, is rare. We here describe two new genera of Phylini (Miridae : Phylinae) – Xiphoidellus, gen. nov. from Australia with six included species, and the monotypic Ampimpacoris, gen. nov. from Argentina. Xiphoidellus shows relationships to taxa in New Zealand and southern South America. Two sets of cladistic analyses, using equal and implied weights approaches, analyse relationships of the seven new species and 19 or 29 additional phyline taxa using 54 and 45 morphological characters, respectively. Both analyses support the New Zealand endemic genus Xiphoides Eyles & Schuh as the sister group to the Australian Xiphoidellus; Araucanophylus pacificus Carvalho from Chile is the sister taxon to the Xiphoides + Xiphoidellus clade. Affinities of the monotypic genus Ampimpacoris, gen. nov. are less clear cut and may be with a clade of Australian plant bugs or a Nearctic taxon. A primary Brooks parsimony analysis, based on one of the tree topologies, resulted in an area cladogram that proposes a close relationship between Australia and New Zealand, with southern South America being the sister to that area. This pattern differs from the classical vicariance pattern reported for many groups of insects, but is consistent with the ‘southern pattern’ frequently observed in plants.


2007 ◽  
Vol 21 (1) ◽  
pp. 73 ◽  
Author(s):  
Jie Wu ◽  
Hong-Zhang Zhou

The genus Priochirus Sharp (Coleoptera : Staphylinidae) is a rove beetle group with great variation in cephalic structures, especially the teeth on the frontal margin of head. In this paper, phylogenetic relationships among ten subgenera of the genus Priochirus sensu lato, and of Priochirus and other genera of the tribe Leptochirini are analysed. A cladistic analysis was conducted based on 62 characters of adult morphology. Results indicate that the genus Priochirus is not a monophyletic group and is divided into two lineages (called here Lineages I and II respectively). The subgenus Euleptarthrus Jakobson, which included three species-groups (japonicus, longicornis and malayanus), is shown to be polyphyletic. Lineage I corresponds with the Leiochirus + (Exochirus + Syncampsochirus) + (Eutriacanthus + (Plastus + (japonicus-group of Euleptarthrus + (Barychirus + Stigmatochirus)))) clade and forms a sister group to the genus Thoracochirus Bernhauer. Lineage II corresponds with the Priochirus, s. str. + (Cephalomerus + (longicornis- and malayanus-group of the Euleptarthrus)) clade. In addition, the analysis reveals sister relationships between representatives of Lineage I and the genus Thoracochirus. On the basis of phylogenetic inference, the genus Plastus Bernhauer, stat. nov. is proposed to include the subgenera of Lineage I and a new subgenus Sinumandibulus, subgen. nov., which is erected for the japonicus-group of the former subgenus Euleptarthrus. The genus Priochirus Sharp sensu novo is redefined to include the subgenera of Lineage II. Seven new species are described from China: Plastus (Sinumandibulus) curvaticornis, sp. nov. from Sichuan; Plastus (Sinumandibulus) recticornis, sp. nov. from Hubei; Priochirus (Euleptarthrus) amblyodontus, sp. nov. from Hunan; Priochirus (Euleptarthrus) baoxingensis, sp. nov. from Sichuan, Priochirus (Euleptarthrus) elongates, sp. nov. from Guizhou, Priochirus (Euleptarthrus) parvicornis, sp. nov. from Fujian and Priochirus (Euleptarthrus) oxygonus, sp. nov. from Hainan.


2011 ◽  
Vol 42 (4) ◽  
pp. 385-409
Author(s):  
Veronica Pereyra

AbstractA phylogenetic analysis of the fungivorous Terebrantia family Merothripidae is performed based on 73 morphological characters and 24 taxa representing the three genera of Merothripidae and outgroups. Heterothrips mexicanus Watson, Heterothripidae; Dorythrips Hood, Melanthripidae; and two genera of Aeolothripidae,Gelothrips Bhatti and Orothrips Moulton represent the outgroup. The Melanthripidae and Aeolothripidae genera are included in order to have a first approximation of the phylogenetic relationships between Merothripidae and these two families (previously suggested to be close relatives). According to the results, the monophyly of Merothripidae is recovered; within Merothripidae, Erotidothrips is the sister group of Damerothrips+Merothrips. Dorythrips is supported as the sister group of Merothripidae, and Aeolothripidae are the sister group to that clade. Additionally, Merothripidae genera are diagnosed and illustrated.


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