scholarly journals RETRACTED ARTICLE: Molecular Phylogeny and Revision of Copepod Orders (Crustacea: Copepoda)

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Sahar Khodami ◽  
J. Vaun McArthur ◽  
Leocadio Blanco-Bercial ◽  
Pedro Martinez Arbizu

Abstract For the first time, the phylogenetic relationships between representatives of all 10 copepod orders have been investigated using 28S and 18S rRNA, Histone H3 protein and COI mtDNA. The monophyly of Copepoda (including Platycopioida Fosshagen, 1985) is demonstrated for the first time using molecular data. Maxillopoda is rejected, as it is a polyphyletic group. The monophyly of the major subgroups of Copepoda, including Progymnoplea Lang, 1948 (=Platycopioida); Neocopepoda Huys and Boxshall, 1991; Gymnoplea Giesbrecht, 1892 (=Calanoida Sars, 1903); and Podoplea Giesbrecht, 1892, are supported in this study. Seven copepod orders are monophyletic, including Platycopioida, Calanoida, Misophrioida Gurney, 1933; Monstrilloida Sars, 1901; Siphonostomatoida Burmeister, 1834; Gelyelloida Huys, 1988; and Mormonilloida Boxshall, 1979. Misophrioida (=Propodoplea Lang, 1948) is the most basal Podoplean order. The order Cyclopoida Burmeister, 1835, is paraphyletic and now encompasses Poecilostomatoida Thorell, 1859, as a sister to the family Schminkepinellidae Martinez Arbizu, 2006. Within Harpacticoida Sars, 1903, both sections, Polyarthra Lang, 1948, and Oligoarthra Lang, 1948, are monophyletic, but not sister groups. The order Canuelloida is proposed while maintaining the order Harpacticoida s. str. (Oligoarthra). Cyclopoida, Harpacticoida and Cyclopinidae are redefined, while Canuelloida ordo. nov., Smirnovipinidae fam. nov. and Cyclopicinidae fam. nov are proposed as new taxa.

2007 ◽  
Vol 76 (1) ◽  
pp. 35-54 ◽  
Author(s):  
Francesca Benzoni ◽  
Fabrizio Stefani ◽  
Jaroslaw Stolarski ◽  
Michel Pichon ◽  
Guillaume Mitta ◽  
...  

The phylogenetic relationships of the scleractinian genus Psammocora with the other genera traditionally included in the family Siderastreidae and some Fungiidae are assessed based on combined skeletal and molecular data. P. explanulata differs from the other examined congeneric species (P. contigua, P. digitata, P. nierstraszi , P. profundacella, P. superficialis, and P. stellata) in possessing interstomatous septa between adult corallites, costae, and in having continuous buttress-like structures joining septal faces (i.e., fulturae) which typically occur in fungiids. These characters are shared with Coscinaraea wellsi but not with the remainder of the examined siderastreids (the congeneric C. columna, and Anomastraea irregularis, Horastrea indica, Pseudosiderastrea tayamai, Siderastrea savignyana) whose septa are interconnected by typical synapticulae. Most of the examined species form septa with distinct transverse groups of centers of calcification, a biomineralization pattern typical of the Robusta clade. The observations on skeletal structures corroborate the results of the ITS2 and 5.8S molecular phylogeny. C. wellsi and P. explanulata are phylogenetically very close to each other and show closer genetic affinity with the examined Fungiidae (Halomitra pileus, Herpolitha limax, Fungia paumotensis, and Podabacia crustacea) than with the other species in the genera Psammocora and Coscinaraea, or with any other siderastreid. Our results show that neither Psammocora nor Coscinaraea are monophyletic genera. The high genetic distances between the species of Siderastreidae, especially between Pseudosiderastrea tayamai and Siderastrea savignyana on one side and the other genera on the other, suggest a deep divergence in the phylogenetic structure of the family.


2020 ◽  
Vol 62 (3-4) ◽  
pp. 293-307
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
M.-H. Jeong ◽  
S.-O. Oh ◽  
A. S. Kondratiuk ◽  
...  

Three genera new for science, i.e. Candelinella S. Y. Kondr. for the Candelariella makarevichiae group, Opeltiella S. Y. Kondr. for the Candelaria fraudans group, as well as Protocandelariella Poelt, D. Liu, J.-S. Hur et S. Y. Kondr. for the Candelariella subdeflexa group are proposed for robust monophyletic branches of the Candelariaceae on the basis of three-gene phylo- geny (i.e. concatenated nrITS, 12S mtSSU and 28S nrLSU sequences). Eight new combinations, i.e. Candelinella makarevichiae (for Candelariella makarevichiae S. Y. Kondr., L. Lokos et J.-S. Hur), Candelinella deppeanae (for Candelariella deppeanae M. Westb.), Opeltiella fraudans (for Candelaria fraudans Poelt et Oberw.), Opeltiella fibrosoides (for Candelaria fibrosoides M. Westb. et Froden), Opeltiella rubrisoli (for Candelariella rubrisoli D. Liu et J.-S. Hur), Opeltiella canadensis (for Candelariella canadensis H. Magn.), Protocandelariella subdeflexa (for Lecanora subdeflexa Nyl.), Protocandelariella blastidiata (for Candelariella blastidiata L. Yakovchenko) are provided.Molecular data provided for Candelinella makarevichiae (including holotype and iso- type), as well as additional specimens of Candelaria asiatica from South Korea for the first time. The latter species (Candelaria asiatica) from China, as well as’Candelaria’ murrayi from Argentina, South America are recorded for the first time. Voucher of Candelariella vitellina from Antarctica is also identified based on molecular phylogeny. It is for the first time shown that ’Candelaria’murrayi is positioned in the outermost position to Candelaria s. str. branch of the phylogenetic tree of the Candelariaceae, and may belong to another genus. Status of the ’Candelariella’medians group, the’Candelariella’ placodizans group, as well as single species ’Candelariella’reflexa and’Candelaria’ pacifica, forming separate branches outside the Candelariella s. str. and Candelaria s. str. clades, will be clarified when additional molecular data will be accumulated. Candelariella subsquamulosa D. Liu et Hur, recently described from South Korea (Liu et al. 2019), proved to be a new synonym of Candelinella makarevichiae.


2015 ◽  
Vol 29 (5) ◽  
pp. 473 ◽  
Author(s):  
Takafumi Nakano ◽  
Son Truong Nguyen

The family Salifidae is a predaceous leech taxon in the suborder Erpobdelliformes. Although Salifidae is widely distributed in the African, Oriental, Indo-Malayan, Sino-Japanese and Australasian regions, the phylogenetic relationships of the family Salifidae have never been tested using molecular data obtained from leeches collected from the family distributional range. A salifid species was collected for the first time in Vietnam, and relevant morphological and molecular data are presented here. Because the Vietnamese salifid species possesses unique morphological characteristics among the known salifid species, this species is herein described as a new species, Salifa motokawai, sp. nov. Phylogenetic analyses based on nuclear 18S rRNA and histone H3, as well as mitochondrial cytochrome c oxidase subunit I, tRNACys, tRNAMet, 12S rRNA, tRNAVal, 16S rRNA, tRNALeu and NADH dehydrogenase subunit 1 markers demonstrate that the Vietnamese salifid species is a close congener with the African Salifa perspicax and the Malagasy Linta be. Furthermore, molecular data revealed non-monophyly of the Asian salifid leeches. According to the observed phylogenetic relationships and morphological characteristics of the Vietnamese Salifa motokawai, sp. nov., the current classification of salifid taxa should be revised.


2021 ◽  
Vol 63 (3-4) ◽  
pp. 351-390
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
I. Kärnefelt ◽  
A. Thell ◽  
M.-H. Jeong ◽  
...  

Seven genera new to science, i.e.: Helmutiopsis, Huriopsis, Johnsheardia, Klauskalbia, Kudratovia, Kurokawia and Poeltonia of the Physciaceae are proposed for the ‘Rinodina’ atrocinerea, the ‘Rinodina’ xanthophaea, the ‘Rinodina’ cinnamomea, the ‘Heterodermia’ obscurata, the ‘Rinodina’ straussii, the ‘Anaptychia’ isidiata and the ‘Physconia’ grisea groups consequently that all form strongly supported monophyletic branches in a phylogeny analysis based on a combined matrix of nrITS and mtSSU sequences. Phylogenetic positions of species belonging to the genera Kashiwadia s. l., Leucodermia, Mischoblastia,Oxnerella, Phaeorrhiza s. l., Polyblastidium and Rinodinella s. l. are discussed. Oxnerella afghanica which for the first time recorded as parasitic lichen species from both epiphytic and saxicolous crustose lichens is designated as type species for the genus Oxnerella. Sequences of the recently described Physcia orientostellaris as well as Huriopsis xanthophaea and additional sequences of Kashiwadia aff. orientalis and Mischoblastia aff. oxydata are submitted to the GenBank. The positions of Polyblastidium casaterrinum from Costa Rica, ‘Rinodina’ efflorescens from Białowieża, Poland, and ‘Mischoblastia’ confragosula from Cambodia in the Physciaceae are confirmed in a phylogeny analysis based on the nrITS sequences. The presence of ‘extraneous mycobiont DNA’ in lichen associations is exemplified with earlier incorrect identifications of Heterodermia, Kashiwadia, Kurokawia,Oxnerella and Poeltonia specimens. Fifty-six new combinations are presented: Helmutiopsis alba (for Rinodina alba Metzler ex Arn.), Helmutiopsis aspersa (for Lecanora aspersa Borrer), Helmutiopsis atrocinerea (for Parmelia atrocinerea Fr.), Huriopsis chrysidiata (for Rinodina chrysidiata Sheard), Huriopsis chrysomelaena (for Rinodina chrysomelaena Tuck.), Huriopsis lepida (for Lecanora lepida Nyl.), Huriopsis luteonigra (for Rinodina luteonigra Zahlbr.), Huriopsis plana (for Rinodina plana H. Magn.), Huriopsis thiomela (for Lecanora thiomela Nyl.), Huriopsis xanthomelana (for Rinodina xanthomelana Müll. Arg.), Huriopsis xanthophaea (for Lecanora xanthophaea Nyl.), Johnsheardia cinnamomea (for Rinodina mniaroea var. cinnamomea Th. Fr.), Johnsheardia herteliana (for Rinodina herteliana Kaschik), Johnsheardia jamesii (for Rinodina jamesii H. Mayrhofer), Johnsheardia reagens (for Rinodina reagens Matzer et H. Mayrhofer), Johnsheardia zwackhiana (for Lecanora zwackhiana Kremp.), Kashiwadia austrostellaris (for Physcia austrostellaris Elix), Kashiwadia jackii (for Physcia jackii Moberg), Kashiwadia littoralis for Physcia littoralis Elix), Kashiwadia nubila (for Physcia nubila Moberg), and Kashiwadia tropica (for Physcia tropica Elix), Klauskalbia crocea (for Heterodermia crocea R. C. Harris), Klauskalbia flabellata (for Parmelia flabellata Fée), Klauskalbia obscurata (for Physcia speciosa (Wulfen) Nyl. *obscurata Nyl.), Klauskalbia paradoxa (for Heterodermia paradoxa Schumm et Schäfer-Verwimp), Kudratovia bohlinii (for Rinodina bohlinii H. Magn.), Kudratovia candidogrisea (for Rinodina candidogrisea Hafellner, Muggia et Obermayer), Kudratovia luridata (for Buellia luridata Körb.), Kudratovia metaboliza (for Rinodina metaboliza Vain.), Kudratovia pycnocarpa (for Rinodina pycnocarpa H. Magn.), Kudratovia roscida (for Lecanora roscida Sommerf.), Kudratovia straussii (for Rinodina straussii J. Steiner), Kudratovia terrestris (for Rinodina terrestris Tomin), Kurokawia bryorum (for Anaptychia bryorum Poelt), Kurokawia isidiata (for Anaptychia isidiata Tomin), Kurokawia mereschkowskii (for Physcia mereschkowskii Tomin), Kurokawia palmulata (for Psoroma palmulatum Michx.), Kurokawia runcinata (for Lichen runcinatus With.), Kurokawia stippea (for Parmelia aquila var. stippea Ach.), Lecania safavidiorum (for Oxnerella safavidiorum S. Y. Kondr., Zarei-Darki, Lőkös et Hur), Leucodermia erinacea (for Lichen erinaceus Ach.), Mischoblastia confragosula (for Lecanora confragosula Nyl.), Mischoblastia destituta (for Lecidea destituta Nyl.), Mischoblastia moziana (for Lecanora moziana Nyl.), Mischoblastia moziana subsp. parasitica (comb. et stat. nova for Rinodina moziana var. parasitica Kaschik et H. Mayrhofer), Mischoblastia ramboldii (for Rinodina ramboldii Kaschik), Mischoblastia vezdae (for Rinodina vezdae H. Mayrhofer), Oxnerella afghanica (for Rinodina afghanica M. Steiner et Poelt), Oxnerella castanomelodes (for Rinodina castanomelodes H. Mayrhofer et Poelt), Physciella nigricans (for Lecanora nigricans Flörke), Poeltonia elegantula (for Physconia elegantula Essl.), Poeltonia grisea (for Lichen griseus Lam.), Poeltonia isidiomuscigena (for Physconia isidiomuscigena Essl.), Poeltonia perisidiosa (for Physcia perisidiosa Erichsen), Poeltonia venusta (for Parmelia venusta Ach.), and Polyblastidium albicans (for Parmelia albicans Pers.) are proposed.


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.


Plant Disease ◽  
2016 ◽  
Vol 100 (9) ◽  
pp. 1813-1822 ◽  
Author(s):  
Maria Luisa Raimondo ◽  
Francesco Lops ◽  
Antonia Carlucci

The genus Biscogniauxia is paraphyletic to members of the family Xylariaceae and includes at least 52 species to date that are mainly pathogens of dicotyledonous angiosperm trees. Most of these are forest trees, such as those in the genera Acacia, Acer, Alnus, Eucalyptus, Fraxinus, Populus, and Quercus, and other species of minor importance. Biscogniauxia spp. have been reported as endophytes or secondary invaders that attack only stressed plants. During a survey in rosaceous orchards in southern Italy, several charcoal cankers were observed and stroma samples were collected. A collection of 31 Biscogniauxia isolates was analyzed. Their phylogenetic relationships were determined through study of the internal transcribed spacer, β-tubulin, and actin gene sequences. Combining morphological, cultural, and molecular data, a new species of Biscogniauxia is described here as Biscogniauxia rosacearum. This new species was isolated for the first time from rosaceous hosts in Apulia. Pathogenicity tests showed that it causes symptoms on stems when artificially inoculated and produces stromata on the bark surface.


2014 ◽  
Vol 51 (3) ◽  
pp. 236-245 ◽  
Author(s):  
K. Quiazon ◽  
T. Yoshinaga ◽  
H. Doi ◽  
J. Araki ◽  
K. Ogawa

Abstract Finding male philometrid nematodes is essential for taxonomic identification among congeneric species. In this study, male Philometra thaiensis Moravec, Fiala et Dyková, 2004 were collected and described for the first time, from the body cavity of the freshwater fish (eyespot pufferfish) Tetraodon biocellatus Tirant (Tetraodontiformes, Tetraodontidae), and conspecific females were redescribed based on the additional morphological biometrics examined. Molecular examination was carried out on the small subunit 18S rRNA, revealing the evolutionary relationships of P. thaiensis and reported philometrid species (Philometra and Philometroides) from Japan with other dracunculoids deposited in the GenBank. Based on the molecular data, there are some genera (Philometra, Philometroides, Clavinema, and Margolisianum [genus inquirendum]) requiring further morphological re-evaluation that should be supported with molecular data.


2021 ◽  
Vol 78 ◽  
pp. 1-16
Author(s):  
Firouzeh Bordbar ◽  
Tim M. Upson

A review of the native Iranian species of Lavandula is presented, including the first recorded occurrence of L. pubescens, new distribution records for L. coronopifolia, and a detailed description and observations of the poorly known endemic L. sublepidota. The phylogenetic relationships of several taxa, including Lavandula sublepidota and L. hasikensis from Oman, are investigated for the first time using molecular data (matK and ITS regions), and changes to the sectional classification are proposed.


2006 ◽  
Vol 17 (3) ◽  
Author(s):  
Ignacio Ribera ◽  
Sergio Montagud ◽  
Santiago Teruel ◽  
Xavier Bellés

The phylogenetic relationships of Ildobates neboti Español (Coleoptera: Carabidae: Harpalinae) were investigated based on three nuclear genes (full 18S rRNA, and a fragment of each 28S rRNAand wingless).We compiled a data set using published sequences of 32 members of Harpalinae including one example each of Dryptini (genus Desera), Galeritini (Galerita) and Zuphiini (Thalpius), plus three Brachininae as outgroups. These three tribes form the “Dryptitae”, within which various relationships of Ildobates had been proposed. The analyses of the datamatrix using parsimony (with equally weighted and reweighted characters) and Bayesian posterior probabilities all support the monophyly of the three tribes in “Dryptitae”, as well as a closest relationship of Ildobates with Thalpius to the exclusion of Desera plus Galerita. This confirms the previous inclusion of Ildobates among the Zuphiini, and corroborates current taxonomic classifications based on morphological criteria.


2021 ◽  
Author(s):  
Hai-Xia Ma ◽  
Zi-Kun Song ◽  
Xiao-Yan Pan ◽  
Zhi Qu ◽  
Si-Yu Ma ◽  
...  

Abstract A study of the phylogeny and taxonomy of Xylaria species associated with fallen fruits and seeds within the genus Xylaria and among gernera of the family Xylariaceae based on ITS, RPB2, and β-tubulin sequences of 97 species from Xylaria and 7 other genera of the Xylariaceae were analyzed. The 7 genera included Amphirosellinia, Astrocystis, Kretzschmaria, Nemania, Podosordaria, Poronia, and Rosellinia. The results of our phylogenetic study showed that Xylaria species were distributed among five major clades, X1, X2, X3, X4, and X5. Clade X1 encompassed exclusively those Xylaria speices associated with termite nests, clade X2 composed Xylaria speices growing on leaves, fibrous pericarps and some on wood, clade X3 contained endocarp-inhabiting Xylaria species, clade X4 composed primarily of wood-inhabiting Xylaria speices, clade X5 composed primarily of species of Xylaria associated with leguminous pods. Xylaria appears to be a paraphyletic genus, with most of 7 genera included in it. Nine new taxa associated with fallen fruits and seeds, namely X. aleuriticola, X. cordiicola, X. meliicola, X. microcarpa, X. rogersii, X. schimicola, X. terminaliicola, X. theaceicola, and X. wallichii, are described, illustrated, and compared to morphologically similar species. Four species, X. carpophila, X. liquidambaris, X. oxyacanthae, and X. xanthinovelutina, were reported in China for the first time. A key to all the accepted species associated with fallen fruits and seeds in Xylaria from China was given.


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