New and noteworthy lichen-forming and lichenicolous fungi 10

2020 ◽  
Vol 62 (1-2) ◽  
pp. 69-108
Author(s):  
S. Y. Kondratyuk ◽  
D. K. Upreti ◽  
G. K. Mishra ◽  
S. Nayaka ◽  
K. K. Ingle ◽  
...  

Eight species, new for science, i.e.: Lobothallia gangwondoana S. Y. Kondr., J.-J. Woo et J.-S. Hur and Phyllopsora dodongensis S. Y. Kondr. et J.-S. Hur from South Korea, Eastern Asia, Ioplaca rinodinoides S. Y. Kondr., K. K. Ingle, D. K. Upreti et S. Nayaka, Letrouitia assamana S. Y. Kondr., G. K. Mishra et D. K. Upreti, and Rusavskia indochinensis S. Y. Kondr., D. K. Upreti et S. Nayaka from India and China, South Asia, Caloplaca orloviana S. Y. Kondr. and Rusavskia drevlyanica S. Y. Kondr. et O. O. Orlov from Ukraine, Eastern Europe, as well as Xanthoria ibizaensis S. Y. Kondr. et A. S. Kondr. from Ibiza Island, Spain, Mediterranean Europe, are described, illustrated and compared with closely related taxa. Fominiella tenerifensis S. Y. Kondr., Kärnefelt, A. Thell et Feuerer is for the first time recorded from Mediterranean Europe, Huriella loekoesiana S. Y. Kondr. et Upreti is provided from Russia for the first time, and H. pohangensis S. Y. Kondr., L. Lőkös et J.-S. Hur for the first time from China, Phoma candelariellae Z. Kocakaya et Halıcı is new to Ukraine, and Staurothele frustulenta Vain. is recorded from the Forest Zone of Ukraine for the first time. Twelve new combinations, i.e.: Bryostigma apotheciorum (for Sphaeria apotheciorum A. Massal.), Bryostigma biatoricola (for Arthonia biatoricola Ihlen et Owe-Larss.), Bryostigma dokdoense (for Arthonia dokdoensis S. Y. Kondr., L. Lőkös, B. G. Lee, J.-J. Woo et J.-S. Hur), Bryostigma epiphyscium (for Arthonia epiphyscia Nyl.), Bryostigma lobariellae (for Arthonia lobariellae Etayo), Bryostigma lapidicola (for Lecidea lapidicola Taylor), Bryostigma molendoi (for Tichothecium molendoi Heufl. ex Arnold), Bryostigma neglectulum (for Arthonia neglectula Nyl.), Bryostigma parietinarium (for Arthonia parietinaria Hafellner et Fleischhacker), Bryostigma peltigerinum (for Arthonia vagans var. peltigerina Almq.), Bryostigma phaeophysciae (for Arthonia phaeophysciae Grube et Matzer), Bryostigma stereocaulinum (for Arthonia nephromiaria var. stereocaulina Ohlert), are proposed based on results of combined phylogenetic analysis based on mtSSU and RPB2 gene sequences. Thirty-one new combinations for members of the genus Polyozosia (i.e.: Polyozosia actophila (for Lecanora actophila Wedd.), Polyozosia agardhiana (for Lecanora agardhiana Ach.), Polyozosia altunica (for Myriolecis altunica R. Mamut et A. Abbas), Polyozosia antiqua (for Lecanora antiqua J. R. Laundon), Polyozosia bandolensis (for Lecanora bandolensis B. de Lesd.), Polyozosia behringii (for Lecanora behringii Nyl.), Polyozosia caesioalutacea (for Lecanora caesioalutacea H. Magn.), Polyozosia carlottiana (for Lecanora carlottiana C. J. Lewis et Śliwa), Polyozosia congesta (for Lecanora congesta Clauzade et Vězda), Polyozosia eurycarpa (for Lecanora eurycarpa Poelt, Leuckert et Cl. Roux), Polyozosia expectans (Lecanora expectans Darb.), Polyozosia flowersiana (Lecanora flowersiana H. Magn.), Polyozosia fugiens (for Lecanora fugiens Nyl.), Polyozosia invadens (for Lecanora invadens H. Magn.), Polyozosia juniperina (for Lecanora juniperina Śliwa), Polyozosia latzelii (for Lecanora latzelii Zahlbr.), Polyozosia liguriensis (for Lecanora liguriensis B. de Lesd.), Polyozosia massei (for Myriolecis massei M. Bertrand et J.-Y. Monnat), Polyozosia mons-nivis (for Lecanora mons-nivis Darb.), Polyozosia oyensis (for Lecanora oyensis M.-P. Bertrand et Cl. Roux), Polyozosia percrenata (for Lecanora percrenata H. Magn.), Polyozosia persimilis (for Lecanora hagenii subsp. persimilis Th. Fr.), Polyozosia poeltiana (for Lecanora poeltiana Clauzade et Cl. Roux), Polyozosia prominens (for Lecanora prominens Clauzade et Vězda), Polyozosia prophetae-eliae (for Lecanora prophetae-eliae Sipman), Polyozosia salina (for Lecanora salina H. Magn.), Polyozosia schofieldii (for Lecanora schofieldii Brodo), Polyozosia sverdrupiana (for Lecanora sverdrupiana Øvstedal), Polyozosia torrida (for Lecanora torrida Vain.), Polyozosia wetmorei (for Lecanora wetmorei Śliwa), Polyozosia zosterae (for Lecanora subfusca? zosterae Ach.)) are proposed.

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.


Phytotaxa ◽  
2013 ◽  
Vol 144 (1) ◽  
pp. 1 ◽  
Author(s):  
Alexander P. Sukhorukov ◽  
Pertti Uotila ◽  
Mingli Zhang ◽  
Hong-Xiang Zhang ◽  
Anna S. Speranskaya ◽  
...  

Two new combinations are proposed in Oxybasis (Chenopodioideae, Chenopodiaceae or Amaranthaceae s.l.). Chenopodium micranthum, described from Russia in the 1860s and known as C. urbicum subsp. sinicum in China, is assigned specific rank in Oxybasis. It appears to be widespread in China, Mongolia, Kazakhstan and Asiatic Russia. The Siberian-Mongolian C. gubanovii, recently described as a new species in Chenopodium sect. Pseudoblitum, is also assigned to Oxybasis. Molecular phylogenetic analysis using maximum likelihood (ML) and maximum parsimony (MP) methods confirmed the placement of C. micranthum and C. gubanovii in the genus Oxybasis. Distribution maps of O. micrantha and O. gubanovii are provided, the latter species being reported for the first time in the Chinese part of the Altai Mountains. A lectotype for C. micranthum (= O. micrantha) is designated.


2021 ◽  
Vol 9 ◽  
Author(s):  
Juan Guerrero ◽  
Manuel Pozas ◽  
Antonio S Ortiz

Donacaula niloticus (Zeller, 1867) is known from south-eastern Europe, Middle East and Turkey to Central Asia, northern India and China and widely distributed in North Africa (Morocco, Algeria, Libya and Egypt). Donacaula niloticus (Zeller 1867) is recorded for the first time from the Iberian Peninsula and the first DNA barcode sequence is published and compared with other European and North American Donacaula species.


Zootaxa ◽  
2019 ◽  
Vol 2717 (1) ◽  
pp. 1 ◽  
Author(s):  
JIRI HULCR ◽  
A. I. COGNATO

As part of an ongoing genus-level revision of Xyleborini (Coleoptera, Curculionidae: Scolytinae), we combined a recent molecular phylogenetic analysis of the tribe (Cognato et al., 2011) with extensive analysis of  morphological characters (over 44,000 representatives of 281 putative species of Xyleborini examined, including 264 types). For the first time, an operational species concept of Xyleborini is explicitly addressed.        The following new genera are proposed: Debus Hulcr and Cognato, gen. n.Fortiborus Hulcr and Cognato, gen. n.Planiculus Hulcr and Cognato, gen. n.Truncaudum Hulcr and Cognato, gen. n.Wallacellus Hulcr and Cognato, gen. n.         Thirty one new combinations and 29 synonymies are given. Cyclorhipidion pelliculosum (Eichhoff), comb. n.Cyclorhipidion sus (Schedl), comb. n.Debus adusticollis (Motschulsky), comb. n.Debus emarginatus (Eichhoff), comb. n.Debus fallax (Eichhoff), comb. n. (=Xyleborus fastigatus Schedl, syn. n.)Debus pseudocylindricus (Eggers) comb. n.Debus pumilus (Eggers), comb. n. (=Xyleborus ipidia Schedl, syn. n., =Xyleborus cylindricus Eggers, syn. n.)Debus spinicornis (Schedl), comb. n.Euwallacea funereus (Lea), comb. n.Fortiborus anisopterae (Browne), comb. n.Fortiborus indigens (Schedl), comb. n.Fortiborus major (Stebbing), comb. n. (=Xyleborus siclus Schedl syn. n.)Fortiborus pilifer (Eggers), comb. n.(= Xyleborus pseudopilifer Schedl, syn. n.)Fortiborus sulcinoides (Schedl), comb. n.Microperus diversicolor (Eggers), comb. n. (Coptodryas atava (Schedl), syn. n., =Microperus myristicae (Schedl) syn. n.)Microperus intermedius (Eggers), comb. n. (=Coptodryas nitella (Browne), syn. n.)Microperus parvus (Lea), comb. n. (=Coptodryas libra (Eggers), syn. n., =Coptodryas pubipennis (Schedl), syn. n.)Microperus pometianus (Schedl), comb. n.Planiculus aries (Schedl), comb. n.Planiculus bicolor (Blandford), comb. n. (=Euwallacea filiformis (Schedl), syn. n., =Euwallacea laevis (Eggers), syn. n., =Euwallacea tumidus (Schedl), syn. n., =Xyleborus glabratulus Browne, syn. n.)Planiculus immersus (Schedl), comb. n. (=Xyleborus hashimotoi Browne, syn. n.)Planiculus limatus (Schedl), comb. n. (=Euwallacea subemarginatus (Eggers), syn. n., Euwallacea subparallelus (Eggers), syn. n.)Truncaudum agnatum (Eggers), comb. n. (=Cyclorhipidion delicatum (Schedl), syn. n., =Cyclorhipidion subagnatum Wood, syn. n., =Xyleborus gratiosus Schedl, syn. n.)Truncaudum impexum (Schedl), comb. n. (=Xyleborus dentatulus Browne, syn. n., =Xyleborus circumspinosus Schedl, syn. n., =Xyleborus falcarius Schedl, syn. n., =Xyleborus subdentatulus Browne, syn. n., =Xyleborus vernaculus Schedl, syn. n., =Xyleborus putputensis Browne, syn. n.)Truncaudum longior (Eggers), comb. n. (=Xyleborus canarivorus Browne, syn. n., =Xyleborus protii Browne, syn. n., =Xyleborus viaticus Schedl, syn. n.)Wallacellus piceus (Motschulsky), comb. n.Wallacellus similis (Ferrari), comb. n.Wallacellus striatulus (Browne), comb. n.The following species are given new status:Cyclorhipidion perlaetum (Schedl), resurrected replacement nameXyleborus judenkoi (Schedl), resurrected name.         We confirm the generic status of Cyclorhipidion californicum (Wood), comb. n.


2019 ◽  
Vol 104 (3) ◽  
pp. 339-354 ◽  
Author(s):  
Barış Özüdoğru ◽  
Kurtuluş Özgişi ◽  
Burcu Tarıkahya-Hacıoğlu ◽  
Atilla Ocak ◽  
Klaus Mummenhoff ◽  
...  

Noccaea Moench is taxonomically one of the most problematic genera of the Brassicaceae. The radical revision of Thlaspi L. s.l. by Meyer in 1973 (Meyer, 1973) split it into 12 segregate genera, including Noccaea, but subsequent molecular studies suggested that this complex includes at least four unrelated genera (Thlaspi s. str., Mummenhoffia Esmailbegi & Al-Shehbaz, Noccidium F. K. Mey., and Noccaea). Although several taxonomic treatments have since been proposed to sort out the systematic problems of Noccaea, debates are still ongoing. Some authors have argued that all segregates of Thlaspi should be considered as independent but related genera, whereas others recognize them as synonyms of a large and polymorphic Noccaea. In this study, we present the first extensively sampled phylogenetic analysis of tribe Coluteocarpeae (Thlaspi segregates including Noccaea) using internal transcribed spacer (ITS) DNA sequences from 92 of the ca. 130 species (70%) in the tribe (39 studied here for the first time) and plastidic trnL-F regions from 73 species (42 studied here for the first time), representing the full range of morphological variation and geographical distribution. All main clades are discussed in detail, and the taxonomic status of all Thlaspi s.l. segregates is evaluated against recent taxonomic treatments. In particular, the tribal placement of Noccidium is changed to Coluteocarpeae, and the genus Pseudosempervivum (Boiss.) Grossh. is reduced to synonymy of Noccaea. The new name N. mummenhoffiana Özüdoğru & Al-Shehbaz and the new combinations N. aucheri (Boiss.) Özüdoğru & Al-Shehbaz and N. sempervivum (Boiss. & Balansa) Özüdoğru & Al-Shehbaz are proposed.


Zootaxa ◽  
2021 ◽  
Vol 5082 (5) ◽  
pp. 401-424
Author(s):  
ERKI ÕUNAP ◽  
SEI-WOONG CHOI ◽  
ALEXEY MATOV ◽  
TOOMAS TAMMARU

Nola estonica Õunap sp. nov. (Lepidoptera, Nolidae, Nolinae) is described based on type material from Estonia. The lectotype is designated for Glaphyra atomosa Bremer, 1861, which is reinstated from a subspecies of Nola aerugula (Hübner, [1793]) to a full species: Nola atomosa (Bremer, 1861) stat. rev. The status of these three taxa as separate species is supported by the results of phylogenetic analysis of DNA barcodes, as well as external and genital morphology of adult specimens. Two new synonyms are established as follows: Nola atomosa (Bremer, 1861) = Nola candidalis Staudinger, 1892 syn. nov. and Nola shin Inoue, 1982 syn. nov. N. estonica occurs sympatrically with N. aerugula in Estonia, and with N. atomosa in South Korea and easternmost Russia. While the available data suggest a disjunct distribution of N. estonica (eastern Europe and the temperate Far East), it appears highly possible that the species has a wide transpalaearctic distribution.  


2000 ◽  
Vol 13 (6) ◽  
pp. 845 ◽  
Author(s):  
Lindy W. Cayzer ◽  
Michael D. Crisp ◽  
Ian R. H. Telford

Following a phylogenetic analysis using morphology, Pittosporum is here monographed and recircumscribed as a monophyletic genus, by including the small genus Citriobatus and by excluding a new genus, described in the accompanying paper as Auranticarpa. Within Australia and its associated territories, 20 species are now recognised in Pittosporum, including the four from Citriobatus, three of which are given new combinations (P. spinescens, P. lancifolium and P. multiflorum). Citriobatus linearis requires a new name (P. viscidum). Four species are reinstated or confirmed at species level (P. angustifolium, P. ligustrifolium, P. nativitatis and P. wingii), and P. trilobum is described for the first time.


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.


2020 ◽  
Vol 62 (3-4) ◽  
pp. 225-291
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
S.-O. Oh ◽  
T. O. Kondratiuk ◽  
I. Yu. Parnikoza ◽  
...  

Fourteen species new for science are described, illustrated and compared with closely related taxa. Six species of them are from South Korea, i.e. Bryostigma huriellae S. Y. Kondr. et J.-S. Hur, Caloplaca ulleungensis S. Y. Kondr., L. Lőkös et J.-S. Hur, Enterographa dokdoensis S. Y. Kondr. et J.-S. Hur, Neobrownliella salyangensis S. Y. Kondr. et J.-S. Hur, Rufoplaca aesan- ensis S. Y. Kondr. et J.-S. Hur, Squamulea coreana S. Y. Kondr. et J.-S. Hur, and seven species are from Chile: Caloplaca nothocitrina S. Y. Kondr. et J.-S. Hur, Caloplaca nothoholocarpa S. Y. Kondr. et J.-S. Hur, Caloplaca patagoniensis S. Y. Kondr., S.-O. Oh et J.-S. Hur, Follmannia suborthoclada S. Y. Kondr. et J.-S. Hur, ‘Lecidea’buellielloides S. Y. Kondr. et J.-S. Hur, Mass- jukiella rusavskioides S. Y. Kondr. et J.-S. Hur, Rehmanniella poeltiana S. Y. Kondr. et J.-S. Hur, as well as one species, i.e. Pyrenodesmia vernadskiensis S. Y. Kondr., T. O. Kondratiuk et I. Yu. Parnikoza, similar to Antarctic endemic species Huea coralligera, is from Argentine Islands, Western Antarctic Peninsula. The member of the genus Pyrenodesmia A. Massal. is for the first time confirmed by molecular data from the Antarctic.Eighteen new combinations, i.e. Massjukiella impolita (for Caloplaca impolita Arup), Massjukiella pollinarioides (for Xanthoria pollinarioides L. Lindblom et D. M. Wright), Massjukiella stellata (for Caloplaca stellata Wetmore et Karnefelt), Massjukiella tenax (for Xanthoria tenax L. Lindblom), and Massjukiella tenuiloba (for Xanthoria tenuiloba L. Lindblom), Pyrenodesmia albopruinosa (for Biatorina albopruinosa Arnold), Pyrenodesmia ceracea (for Caloplaca ceracea J. R. Laundon), Pyrenodesmia cretensis (for Blastenia cretensis Zahlbr.), Pyrenodesmia erythrocarpa (for Patellaria erythrocarpa Pers.), Pyrenodesmia haematites (for Lecanora haematitesChaub. ex St.-Amans), Pyrenodesmia percrocata (for Blastenia percrocata Arnold), Pyrenodesmia soralifera (for Caloplaca soralifera Vondrak et Hrouzek), Pyrenodesmia transcaspica (for Lecanora transcaspica Nyl.), Pyrenodesmia viridirufa (for Lecidea viridirufa Ach.), Pyrenodesmia xerica (for Caloplaca xerica Poelt et Vezda), as well as Rehmanniella leucoxantha (for Amphilo-ma leucoxanthum Mull. Arg.), Rehmanniella syvashica (for Caloplaca syvashica Khodos., Vond- rak et Soun), and Rehmanniella subgyalectoides (for Caloplaca subgyalectoides S. Y. Kondr. et Karnefelt) are proposed.Buelliella inops and Zwackhiomyces aff. berengerianus are for the first time recorded from South America as well as from Follmannia orthoclada (as lichenicolous fungi). Caloplaca poliotera, Rinodina convexula and Rinodina kozukensis are new to the Republic of Korea, and new localities as well as illustrations for the further 13 new and rare lichen species recently described from Eastern Asia are provided too.


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