Contributions to Molecular Phylogeny of Lichen-Forming Fungi 2. Review of Current Monophyletic Branches of the Family Physciaceae

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.

Zootaxa ◽  
2017 ◽  
Vol 4312 (2) ◽  
pp. 355 ◽  
Author(s):  
MENGLIN WANG ◽  
THIERRY BOURGOIN ◽  
YALIN ZHANG

Three new Oriental Issidae genera and two new species identified by a previous molecular phylogeny analysis are described. Two new genera belong to the tribe Kodaianellini: Kodaianellissus gen. nov., type species: K. intorqueus sp. nov. from China and Tetricissus gen. nov., type species: T. philo (Fennah, 1978) from Vietnam. Another new genus representing Sarimini: Longieusarima gen. nov., type species: L. lunulia sp. nov. is described from China. 


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.


2021 ◽  
Vol 43 ◽  
pp. 16-29
Author(s):  
Roman V. Yakovlev ◽  
Vadim V. Zolotuhin

In the third part of the revision of the family Metarbelidae (Lepidoptera) of South-Eastern Asia, we provide a revision of the genus Stueningeria Lehmann, 2019 with description of six new species: Stueningeria htetae sp. nov. (Type locality: Mynmar, 21 km E Putao), Stueningeria csovarii sp. nov. (Type locality: Thailand, Changwat Nan, 15 km N of Bo Luang), Stueningeria loeffleri sp. nov. (Type locality: Thailand, Sakhon Nakhon Prov., Phu Pan NP), Stueningeria ihlei sp. nov. (Type locality: Vietnam (C.), Prov. Thua-Thien-Hue, Kreis A Luoi, Gemeinde A Rong, Passastrasse ca. 30 km S A Luoi.), Stueningeria murzini sp. nov. (Type locality: China, SW Yunnan, Xishuanbanna, Guanping env., 60 km N Jinghong), and Stueningeria pinratanai sp. nov. (Type locality: NW Thailand, Chiangmai, Doi Pui Forest Res. Stat.)  Two new combinations are established: Stueningeria campbelli (Hampson, 1910) comb. nov. and Stueningeria phaga (Swinhoe, 1894) comb. nov. Both species are redescribed. The type species of the genus Stueningeria nepalensis Lehmann, 2019 is reported for the first time for the fauna of India (Uttarakhand). We also give for the first time the description of female genitalia of the genus Stueningeria. The genus distribution map is provided.


Phytotaxa ◽  
2018 ◽  
Vol 358 (1) ◽  
pp. 67 ◽  
Author(s):  
PRISCYLLA NAYARA BEZERRA SOBREIRA ◽  
MARCELA EUGENIA DA SILVA CÁCERES ◽  
LEONOR COSTA MAIA ◽  
ROBERT LÜCKING

A new genus of lichenized fungi of the family Porinaceae is described, known from Costa Rica and Brazil. Flabelloporina Sobreira, M. Cáceres & Lücking is a thus far monospecific genus with an isolated position of its only species in the family, morphologically different from all other genera in Porinaceae. The genus is characterized by the production of numerous, flabelliform squamules on the surface of the thallus, together with black perithecia and transversally septate ascospores (with three septa in the only species). The new combination Flabelloporina squamulifera (Breuss, Lücking & Navarro) Sobreira, M. Cáceres & Lücking is proposed, based on Porina squamulifera Breuss, Lücking & Navarro, and the species is for the first time reported from Brazil.


MycoKeys ◽  
2020 ◽  
Vol 74 ◽  
pp. 17-74
Author(s):  
Martina Réblová ◽  
Jana Nekvindová ◽  
Jacques Fournier ◽  
Andrew N. Miller

The Chaetosphaeriaceae are a diverse group of pigmented, predominantly phialidic hyphomycetes comprised of several holomorphic genera including Chaetosphaeria, the most prominent genus of the family. Although the morphology of the teleomorphs of the majority of Chaetosphaeria is rather uniform, their associated anamorphs primarily exhibit the variability and evolutionary change observed in the genus. An exception from the morphological monotony among Chaetosphaeria species is a group characterised by scolecosporous, hyaline to light pink, multiseptate, asymmetrical ascospores and a unique three-layered ascomatal wall. Paragaeumannomyces sphaerocellularis, the type species of the genus, exhibits these morphological traits and is compared with similar Chaetosphaeria with craspedodidymum- and chloridium-like synanamorphs. Morphological comparison and phylogenetic analyses of the combined ITS-28S sequences of 35 isolates and vouchers with these characteristics revealed a strongly-supported, morphologically well-delimited clade in the Chaetosphaeriaceae containing 16 species. The generic name Paragaeumannomyces is applied to this monophyletic clade; eight new combinations and five new species, i.e. P. abietinussp. nov., P. eleganssp. nov., P. granulatussp. nov., P. sabinianussp. nov. and P. smokiensissp. nov., are proposed. A key to Paragaeumannomyces is provided. Using morphology, cultivation studies and phylogenetic analyses of ITS and 28S rDNA, two additional new species from freshwater and terrestrial habitats, Codinaea paniculatasp. nov. and Striatosphaeria castaneasp. nov., are described in the family. A codinaea-like anamorph of S. castanea forms conidia with setulae at each end in axenic culture; this feature expands the known morphology of Striatosphaeria. A chaetosphaeria-like teleomorph is experimentally linked to Dendrophoma cytisporoides, a sporodochial hyphomycete and type species of Dendrophoma, for the first time.


2016 ◽  
Vol 47 (1) ◽  
pp. 53-82 ◽  
Author(s):  
Werner P. Strümpher ◽  
Martin H. Villet ◽  
Catherine L. Sole ◽  
Clarke H. Scholtz

Extant genera and subgenera of the Trogidae (Coleoptera: Scarabaeoidea) are reviewed. Contemporary classifications of this family have been based exclusively on morphological characters. The first molecular phylogeny for the family recently provided strong support for the relationships between morphologically defined genera and subgenera. On the basis of morphological, molecular and biogeographical evidence, certain taxonomic changes to the genus-level classification of the family are now proposed. The family is confirmed as consisting of two subfamilies, Omorginae Nikolajev and Troginae MacLeay, the former with two genera,OmorgusErichson andPolynoncusBurmeister, and the latter with two genera,TroxFabricius andPhoberusMacLeaystat. rev.Phoberusis restored to generic rank to include all Afrotropical (including Madagascan endemic) species;Afromorgusis confirmed at subgeneric rank within the genusOmorgus; and the monotypic Madagascan genusMadagatroxsyn. n.is synonymised withPhoberus.The current synonymies ofPseudotroxRobinson (withTrox),ChesasBurmeister,LagopelusBurmeister andMegalotroxPreudhomme de Borre (all withOmorgus) are all accepted to avoid creating speculative synonyms before definitive phylogenetic evidence is available. New combinations resulting from restoringPhoberusto a monophyletic genus are listed in Appendix A.


Zootaxa ◽  
2021 ◽  
Vol 5060 (1) ◽  
pp. 1-44
Author(s):  
ELENA V. MIKHALJOVA

The family Diplomaragnidae Attems, 1907 of the Asian part of Russia is reviewed and shown to comprise 11 genera and 60 species + 1 dubious species. Two genera and seven species are described here as new to science: Alineuma gen. nov., with type species A. rodionovi sp. nov. and Litovkia gen. nov., with the type species L. anisimovka sp. nov., Diplomaragna budilovi sp. nov., Diplomaragna dentifer sp. nov., Pacifiosoma shabalini sp. nov., Pacifiosoma acutum sp. nov., Pacifiosoma triangulatum sp. nov. Pacifiosoma asperum Mikhaljova, 2016 is recorded from the Primorsky Krai for the first time. Five genera are endemic to the Asian part of Russia. At the species level, the rate of endemism amounts to 91.7%. A key is given to all species of Diplomaragnidae presently known from Siberia and the Russian Far East. The distributions of the region’s diplomaragnids are discussed. Taxonomic remarks are provided for many species.  


Zootaxa ◽  
2009 ◽  
Vol 2318 (1) ◽  
pp. 552-565 ◽  
Author(s):  
PIERFILIPPO CERRETTI ◽  
THOMAS PAPE

A cladistic analysis of the genus Melanophora Meigen, 1803 (type-species: Musca grossificationis Linnaeus, 1758 [= Musca roralis Linnaeus, 1758]) is presented and the generic delimitation is critically redefined. The nominal genus-group taxon Bequaertiana Curran, 1929 (type-species: Bequaertiana argyriventris Curran, 1929) is synonymised with Melanophora Meigen syn. nov. The following new combinations are proposed: Melanophora argyriventris (Curran, 1929) comb. nov. and Melanophora basilewskyi (Peris, 1957) comb. nov. Melanophora chia sp. nov. from SW Sardinia is described, illustrated and compared with the other known species of the genus. The male of Melanophora asetosa Kugler, 1978 is described for the first time. Melanophora basilewskyi (Peris, 1957) is recorded from Kenya for the first time.


Zootaxa ◽  
2018 ◽  
Vol 4434 (2) ◽  
pp. 265
Author(s):  
GEOVANNI M. RODRÍGUEZ-MIRÓN

A checklist of the Megalopodidae of the world is presented. A total of 582 species in 29 genera and 11 subgenera are recognized belonging to the three subfamilies. The subfamilies, genera, and species are listed in alphabetical order. For each species, synonymous names and the geographical distribution by country is provided. The most diversified subfamily is Megalopodinae with 480 species and 24 genera. The Neotropical biogeographic region has the highest diversity of Megalopodidae, followed by the Ethiopian region. The knowledge of Megalopodidae is limited, and is remarkably biased by country. A significant increase in geographic and taxonomic information is needed in order to fill these knowledge gaps. The following taxonomic and nomenclatural changes are proposed: 1) type species are designated for the genera Macrolopha Weise and Falsomegalopus Pic. 2) Zeugophora novobicolor Rodríguez-Mirón is proposed as new replacement name of Zeugophora bicolor. 3) The following taxa are reinstated in the genera Temnaspis: T. speciosus Baly, T. arida Westwood, and T. nigriceps Baly. 4) Falsotemnaspis luteimembris Pic is proposed as new synonym (= F. lacordairei (Westwood)). 5) The next new combinations are proposed: Macrolopha bicolor (Jacoby), M. carinata (Bryant), M. centromaculata (Jacoby), M. costatipennis (Pic), M. dollmani (Bryant), M. hargreavesi (Bryan), M. mashuana (Jacoby), M. murrayi (Baly), M. neavei (Bryant), M. nyassae (Bryant), M. suturalis (Clavareau), M. variabilis (Westwood), M. aeneipennis (Weise), M. notaticollis (Pic), M. parvula (Weswood), M. theresae (Pic), M. tricoloripes (Pic) and Falsotemnaspis lacordairei (Westwood). 


Zootaxa ◽  
2018 ◽  
Vol 4407 (3) ◽  
pp. 383
Author(s):  
VLADIMIR V. DUBATOLOV ◽  
ANTON V. VOLYNKIN ◽  
YASUNORI KISHIDA

The Prabhasa Moore, 1878 genus-group is reviewed. The male and female genitalia of Prabhasa venosa Moore, 1878, the type species of the genus, are described and illustrated for the first time. Two new genera, Macohasa Dubatolov, Volynkin & Kishida, gen. nov. and Chinasa Dubatolov, Volynkin & Kishida, gen. nov. and two new species, Macohasa cernyi Dubatolov, Volynkin & Kishida, sp. nov. and Chinasa sapa Dubatolov, Volynkin & Kishida, sp. nov. are described for Prabhasa venosa sensu authors. Seven new combinations are established: Zadadra plumbeomicans (Hampson, 1894), comb. nov., Zadadra monastyrskyi (Dubatolov, 2012), comb. nov., Macohasa orientalis (Hampson, 1905), comb. nov., Macohasa tetraspila (Černý, 2009), comb. nov., Macohasa dimorpha (Hampson, 1918), comb. nov., Chinasa costalis costalis (Moore, 1878), comb. nov. and Chinasa costalis bicoloriceps (Strand, 1916), comb. nov. 


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