The application of Helotium to agarics. Part I. Nomenclature. Part II. Notes on selected species from Canada

1982 ◽  
Vol 60 (10) ◽  
pp. 1998-2013 ◽  
Author(s):  
S. A. Redhead

The typification of Helotium Tode 1790, is detailed. Tode's comments in the protologue indicated that Helotium hirsutum Tode was the more important species upon which the generic description was based. The earliest explicit (lecto) typification was proposed by Fries in 1825. Fries's selection of Helotium gibbum Alb. & Schw. supports, by proxy, the acceptance of the original Helotium hirsutum as type now that both combinations are recognized as synonyms of each other. Evidence is presented to demonstrate that an attempt by Donk in 1962 to lectotypify Helotium with Helotium glabrum Tode was made arbitrarily, without direct reference to the protologue. A single recent collection is designated as neotype for both H. hirsutum and H. gibbum. Hemimycena crispula (Quél.) Singer is considered to be conspecific hence making the genus Hemimycena sensu Singer a later synonym of Helotium. Shortly after the publication of the name Helotium by Tode, the generic name was applied to both ascomycetes and basidiomycetes by Gmelin in 1792. The formal division of the genus into two, based on rules in the current code of botanical nomenclature, did not occur until 1805 when De Lamarck and De Candolle completed the process started by Persoon in 1799. The type species of Helotium Pers. apud D.L. &D.C. H. aciculare (Bull.) Pers. apud D.L. &D.C. was selected by Fries in 1818. Thirty-two new combinations are proposed in Helotium Tode for species which were mainly Hemimycena previously. Three invalid species names are validated in Helotium and two new names are proposed to avoid the creation of later homonyms. In addition, Helotium cyphelloides sp. nov. on Carex and Helotium nebulophilum sp. nov. on moss are described. Helotium substellatum (Kühner) comb. nov. is reported for the first time from North America and Helotium albicolor (A. H. Smith) comb. nov. with Helotium hirsutum for the first time in Canada. All five occur in British Columbia. Mycena litoralis A. H. Smith is considered to be a synonym of Helotium pseudocrispulum (Kühner) comb. nov. which is recognized for the first time in North America.

2010 ◽  
Vol 42 (5) ◽  
pp. 587-600 ◽  
Author(s):  
Alan M. FRYDAY ◽  
James C. LENDEMER

AbstractThe species assigned to the genus Catillochroma are reassessed. The two characters used to characterize Catillochroma, exciple anatomy and thalline chemistry, are shown to be variable and contradictory with a number of intermediates. Consequently, Catillochroma is reduced to synonymy with Megalaria, and the species previously placed in Catillochroma transferred, or returned, to Megalaria. As such, the following new combinations are proposed: Megalaria anaglyptica, M. endochroma, M. intermiscens and M. leptocheila. The genus Lopezaria is also shown to be related to Megalaria and to be closely related to the type species of Catillochroma, C. endochroma, and so is also reduced to synonymy with Megalaria. A number of species found to have been misplaced in Catillaria are also transferred to Megalaria: M. leucochlora, M. melanopotamica, M. obludens, M. pannosa and M. phaeolomiza. Megalaria imshaugii is reduced to synonymy with M. obludens, Megalaria pannosa is reported for the first time from North America and Lopezaria isidiza is reported for the first time from outside Asia from Jamaica.


1964 ◽  
Vol 42 (6) ◽  
pp. 723-768 ◽  
Author(s):  
Paul Arenz Lemke

The genus Aleurodiscus Rabenh. ex J. Schroet. (sensu lato) is an artificial assemblage of large-spored 'thelephoraceous' hymenomycetes, which can no longer be maintained as a generic unit. The generic limits and the taxonomic position of Aleurodiscus (sensu stricto) (TYPE SPECIES: A. amorphus (Pers. per Purt.: Fr.) J. Schroet.) have been discussed by the writer (1964) in a separate paper. The present work supplements this earlier work, but is concerned primarily with an appraisal of the non-amyloid-spored Aleurodisci, all of which are removed from Aleurodiscus and either assigned to other recognized genera or relegated to new genera.Accordingly, two new genera and 15 new combinations are devised here to accommodate several species formerly placed in Aleurodiscus (sensu lato). The new genera, one of which is monotypical, are Aleurocorticium Lemke, gen. nov. (TYPE SPECIES: A. acerinum (Pers. per Fr.) Lemke, gen. & comb. nov.) and Licrostroma Lemke, gen. nov. (MONOTYPE: L. subgiganteum (Berk.) Lemke, gen. & comb. nov.). The additional 13 combinations proposed are Aleurocorticium album (Viégas) Lemke, comb, nov., A. alliaceum (Quél.) Lemke, comb. nov., A. candidum (Schw.) Lemke, comb. nov. A. dryinum (Pers.) Lemke, comb. nov., A. griseo-canum (Bres.) Lemke, comb. nov., A. lepra (Berk. et Curt.) Lemke, comb. nov., A. macrodens (Coker) Lemke, comb. nov., A. macrosporum (Bres.) Lemke, comb. nov., A. moquiniarum (Viégas) Lemke, comb. nov., A. nivosum (Berk. et Curt. ex Höhn. et Litsch.) Lemke, comb. nov., A. seriatum (Berk. et Curt.) Lemke, comb. nov., A. strumosum (Fr.) Lemke, comb. nov.; and Aleurocystis magnispora (Burt) Lemke, comb. nov.The genus Laeticorticium Donk (1956: 16) (TYPE SPECIES: L. roseum (Pers. per Fr.) Donk) is confirmed as a valid segregate from Aleurodiscus (sensu lato), but the species of Laeticorticium are not treated here aside from nomenclatural considerations. With the exception of the Laeticorticia, all of the remaining North American and many of the critical non-amyloid-spored species of Aleurodiscus (sensu lato) are reviewed.Particular emphasis is devoted to the genus Aleurocorticium Lemke, gen. nov. and a key to 14 North American species of Aleurocorticium is provided. Seven of the Aleurocorticia are reported from the North American mycobiota for the first time. These seven species, five of which are described as new to science, include Aleurocorticium alliaceum (Quél.) Lemke [= Aleurodiscus alliaceus (Quél) Boidin (1957)], Aleurocorticium dryinum (Pers.) Lemke [= Aleurodiscus dryinus (Pers.) Bourd,], Aleurocorticium incrustans Lemke, sp. nov., A. maculatum Jacks. et Lemke, sp. nov., A. mexicanum Lemke, sp. nov., A. microsporum Jacks. et Lemke, sp. nov., and A. pachysterigmatum Jacks. et Lemke, sp. nov.Corlicium hiemale [= Aleurodiscus hiemalis (Laurila) Eriksson (1958a: 78)] is, likewise, initially recorded for North America.Eight of the named species of Aleurodiscus are recognized as facultative synonyms. These names, as indicated, are offered as taxonomic discards: [Aleurodiscus albidus Massee =] Aleurocorticium lepra (Berk. et Curt.) Lemke; [Aleurodiscus albus (Burt) Rogers et Jacks. =] Xenasma clematidis (Bourd. et Galz.) Liberta; [Aleurodiscus guttulatus Rick =] Bourdotia cinerea (Bres.) Bourd. etGalz.; [Aleurodiscus jacksonii Ahmad =] Aleurocorticium candidum (Schw.) Lemke; [Aleurodiscus orientalis Lloyd =] Licrostroma subgiganteum (Berk.) Lemke; [Aleurodiscus reflexus Yasuda =] Licrostroma subgiganteum (Berk.) Lemke; [Aleurodiscus sendaiensis Yasuda =] Corticium evolvens (Fr. ex Fr.) Fr.; [Aleurodiscus subacerinus Höhn. et Litsch. =] Aleurocorticium alliaceum (Quél.) Lemke.The genus Cyphella Fr. (MONOTYPE: C. digitalis (Alb. et Schw. per Pers.) Fr.) is reinstated (see Code 1952: 76) and the combination Aleurodiscus digitalis (Alb. et Schw. per Pers.) Donk (1951: 210) is discredited.


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 ◽  
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 ◽  
2019 ◽  
Vol 4695 (6) ◽  
pp. 568-576
Author(s):  
ANIL KUMAR DUBEY

Takahashi (1942) described Dialeurotrachelus cambodiensis, the type species of the monotypic whitefly genus, Dialeurotrachelus Takahashi from three syntype specimens collected on an unidentified tree in Cambodia, which were subsequently lost or destroyed. It was rediscovered after eight decades in the Indian territories of the Andaman and Nicobar Islands. A neotype is designated for D. cambodiensis Takahashi, from specimens collected on Diospyros kurzii Hiern (Ebenaceae) from Andaman Island, India. It is recorded for the first time from the Indian territories, Andaman and Nicobar Islands. Pupal morphology is assessed for redefining the generic description with differential diagnoses from related genera, and anomalies involved with structure of the vasiform orifice and associated structures are discussed. Illustrations are provided of the puparia in life, camera lucida drawings, slide mounts, and scanning electron photomicrographs. 


Zootaxa ◽  
2017 ◽  
Vol 4234 (1) ◽  
pp. 1 ◽  
Author(s):  
OWEN LONSDALE

The Liriomyza (Diptera: Agromyzidae) of Canada and Alaska is revised, with species keyed and illustrated, and new host and geographic records provided. Eighty one species are recognized, including 24 new to science: L. agrios, L. albispina, L. anatolis, L. aphila, L. apilaca, L. aquapolis, L. arenarium, L. atrassimilis, L. bicolumbis, L. charada, L. cracentis, L. elevaster, L. emaciata, L. fumeola, L. gibsoni, L. griffithsi, L. hilairensis, L. limopsis, L. mesocanadensis, L. pilicornis, L. pistilla, L. rigaudensis, L. taraxanox, L. taraxanuda, L. tryssos. Ten species known from the United States are recorded as new to Canada: L. artemisiae Spencer, L. assimilis (Malloch), L. baccharidis Spencer, L. helianthi Spencer, L. merga Lonsdale, L. minor Spencer, L. sabaziae Spencer, L. temperata Spencer, L. violivora (Spencer) and L. virgo (Zetterstedt). Palaearctic species new to North America include L. wachtli Hendel and L. flaveola (Fallén); while the latter species has been recorded in North America before, all previous records represent misidentifications. Hosts are recorded for the first time for L. balcanicoides Sehgal, L. minor Spencer, L. orilliensis Spencer and L. socialis Spencer. Galiomyza Spencer syn. nov. is included as a junior synonym of Liriomyza Mik, resulting in six new combinations. 


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. 


1992 ◽  
Vol 6 (1) ◽  
pp. 1 ◽  
Author(s):  
AD Austin ◽  
PC Dangerfield

The genera of microgastrine braconid wasps present in the Australasian region (defined as Australia, New Zealand, New Caledonia, New Guinea, Solomon Is, Fiji Is, Samoan Is, Cook Is, but not French Polynesia) are reviewed. An illustrated key to genera, comments on their taxonomy, and information on the distribution and host relationships of species are provided. Following examination of holotypes, the generic placement of all species recorded from the region is reassessed since a recent generic reclassification of the subfamily left most of the Australasian species incorrectly placed. Parapanteles Ashmead (N.T.), Fornicia Brullé (Qld) and Deuterixys Mason (Qld) are recorded from Australasia for the first time, while Buluka De Seager, Parenion Nixon, Snellenius Westwood and Wilkinsonellus Mason, previously known from Australasia, are recorded from mainland Australia for the first time. The genus Austrocotesia is described as new [with A. exigua, sp. nov. (Papua New Guinea) as the type species], along with the following 14 species: Austrocotesia delicata, sp. nov. (Papua New Guinea, Qld), A. paradoxa, sp. nov. (Papua New Guinea), Buluka collessi, sp. nov. (Qld), Deuterixys anica, sp. nov. (Vic., N.S. W., Qld), Fornicia commoni, sp. nov. (Qld), Glyptapanteles deliasa, sp. nov. (S.A.), Microgaster nixoni, sp. nov. (Tas., N.S.W.), Parapanteles masoni, sp. nov. (N.T.), Parenion beelaronga, sp. nov. (Qld), P. bootha, sp. nov. (Qld), Sathon albicoxa, sp. nov. (Tas., Vic., N.S.W.), S. naryciae, sp. nov. (Vic.), Wilkinsonellus amplus, sp. nov. (Qld, N.T.) and W. tomi, sp. nov. (Papua New Guinea, New Britain, Qld). Glyptapanteles guyanensis (Cameron), comb. nov. is excluded from the Australasian fauna; the name Glyptapanteles fullawayi, nom. nov. (Samoa) is proposed for Apanteles opercuiinae var. polita Fullaway; lectotypes are designated for Cotesia deliadis (Bingham), comb. nov. (Qld), C. philoeampa (Cameron), comb. nov. (N.S.W) and C. rufiventris (Bingham), comb. nov. (Qld); Glyptapanteles operculinae (Fullaway), comb. nov. (Samoa), Microgaster kuchingensis Wilkinson (Papua New Guinea) and Sathon moratus (Wilkinson), comb. nov. (Vic., S.A., W.A.) are redescribed; and 41 additional new combinations are proposed.


Zootaxa ◽  
2018 ◽  
Vol 4415 (2) ◽  
pp. 357 ◽  
Author(s):  
DENIS J. BROTHERS

The genus Aglaotilla Brothers, gen. nov., is described for 14 striking species of Australian Mutillidae related to Ephutomorpha André, 1902, characterized by bright metallic coloration and strong punctation. The description of both sexes is possible through sex associations revealed by rearings from mud nests and trap nests. Both sexes of the type species, Ephutomorpha submetallescens Turner, 1916, are described and illustrated, the male for the first time. New combinations and a new name are proposed, as follows: Aglaotilla aeruginosa (Smith, 1879), comb. nov. (from Mutilla); A. australis (André, 1898), comb. nov. (from Mutilla); A. cuprea (André, 1901), comb. nov., stat. nov. (from Mutilla); A. dilecta (Turner, 1916), comb. nov. (from Ephutomorpha); A. ignita (Smith, 1855), comb. nov. (from Mutilla); A. metallica (Smith, 1855), comb. nov. (from Mutilla); A. mira (André, 1895), comb. nov. (from Mutilla (Sphaerophthalma [sic.])); A. nigroaenea (Smith, 1855), comb. nov. (from Mutilla); A. picturata (Turner, 1914), comb. nov. (from Ephutomorpha); A. semicuprea (André, 1898), comb. nov. (from Mutilla); A. submetallescens (Turner, 1916), comb. nov. (from Ephutomorpha); A. viridatis (Smith, 1855), comb. nov. (from Mutilla); A. viridiaurea (André, 1895), comb. nov. (from Mutilla (Sphaerophthalma [sic.])); A. discolor Brothers, nom. nov. (= Ephutomorpha aeneidorsis Turner, 1916, not Ephutomorpha lauta var. aeneidorsis André, 1903). 


1990 ◽  
Vol 68 (11) ◽  
pp. 2338-2351 ◽  
Author(s):  
S. A. Marshall ◽  
Ian P. Smith

All macropterous species of Aptilotus Mik are keyed, with descriptions of two new macropterous North American species, Aptilotus pogophallus and A. nigriphallus. New distributional records are given for other North American species, and brachyptery is noted for the first time in A. luctuosus (Spuler). Four new macropterous species of Aptilotus (glabrifrons, spinistylus, rufiscapus, and binotatus are described from Nepal. The relationships between the North American and Nepalese species are discussed. Minocellina Papp is synonomized with Aptilotus, and the two species formerly in Minocellina, A. thaii (Papp) and A. besucheti (Papp), are thus given as new combinations. Limosina carbonicolor Richards, from Ethiopia, is redescribed and transferred to Aptilotus.


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