Taxonomic remarks on some Asian Lepidium s. l. (Brassicaceae)

Phytotaxa ◽  
2014 ◽  
Vol 186 (2) ◽  
pp. 97 ◽  
Author(s):  
Dmitry A German

Taxonomy of some Central, Middle and South West Asian representatives of Lepidium s. l. is revised and updated. Poorly known taxon, L. rubtzovii, is shown to be unrelated to L. coronopifolium s. l., but close to L. lacerum. Three new combinations (L. lacerum subsp. rubtzovii, L. leventii, and L. macrocarpum) are proposed. The names L. deserti, L. persicum subsp. arianum and L. seravschanicum, and Stroganowia kazachstanica are newly recognized as synonyms of L. obtusum, L. ferganense, and L. cardiophyllum, respectively. For L. ferganense and L. macrocarpum, lectotypes are designated. Besides, L. lacerum subsp. rubtzovii is reported for the first time for China (instead of subsp. lacerum), L. leventii for Iran, L. macrocarpum for Tajikistan, and L. obtusum for Afghanistan. In contrast, occurrence of L. lacerum in Uzbekistan and Turkmenistan is considered doubtful.

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 54 (2) ◽  
pp. 497-513 ◽  
Author(s):  
L. N. Beldiman ◽  
I. N. Urbanavichene ◽  
V. E. Fedosov ◽  
E. Yu. Kuzmina

We studied in detail a moss-lichen component of Shokalsky Island vegetation for the first time and identified 79 species of mosses and 54 species and 2 subspecies of lichens and lichenicolous fungi. All species of mosses and 23 species and 2 subspecies of lichens and lichenicolous fungi are recorded for the first time for the island. The study is based on collections made in South West part of the island, in arctic tundra. We also explored the participation of the mosses and lichens in the main types of plant communities and the species distribution in 10 ecotopes. The paper describes the noteworthy findings (Abrothallus parmeliarum, Aongstroemia longipes, Arthonia peltigerea, Caloplaca caesiorufella, Catillaria stereocaulorum, Ceratodon heterophyllus, Lecanora leptacinella, Sphagnum concinnum, S. olafii) and features of bryo- and lichenoflora of Shokalsky Island.


1976 ◽  
Vol 7 (4) ◽  
pp. 241-251 ◽  
Author(s):  
Ebbe Schmidt Nielsen ◽  
Ole Karsholt

AbstractNotes are given on the identity and synonymy of five species of Lepidoptera described by Linnaeus, twenty-eight by Fabricius and two by Ström. Each species dealt with is treated under the apparent valid combination; for each species reference is given to the original description. Twenty-four new species-group name synonyms are introduced and nine new combinations are established: Nemaxera betulinella (Fabr.), Argyresthia arcella (Fabr.), Depressaria depressana (Fabr.), Chrysoesthia drurella (Fabr.), Brachmia blandella (Fabr.), Acleris laterana (Fabr.), Pseudohermenias abietana (Fabr.), Epinotia abbreviana (Fab.) and Acrobasis repandana (Fabr.). During the work two neotypes, twenty-seven lectotypes and two paralectotypes have been designated and are here cited for the first time.


2008 ◽  
Vol 40 (04) ◽  
pp. 337-362 ◽  
Author(s):  
Einar TIMDAL
Keyword(s):  

Abstract:Twenty species of Phyllopsora are recognized in Peru, 8 of which are described as new: P. atrocarpa, P. brakoae, P. glaucescens, P. labriformis, P. lacerata, P. lividocarpa, P. nigrocincta, and P. soralifera. Four new combinations are proposed: Phyllopsora cinchonarum (Fée) Timdal, P. glaucella (Vain.) Timdal, P. leucophyllina (Nyl.) Timdal, and for an extra-Peruvian species, P. sorediata (Aptroot & Sparrius) Timdal. The genera Squamacidia and Triclinum are synonymized with Phyllopsora and sorediate species are included in the genus for the first time. Phyllopsora chodatinica, P. swinscowii, and the acid deficient chemotype of P. furfuracea are new to the neotropics and P. cuyabensis, P. glaucella and P. leucophyllina are new to Peru. A key to the Peruvian species is provided.


Phytotaxa ◽  
2015 ◽  
Vol 213 (2) ◽  
pp. 87 ◽  
Author(s):  
Kazem Negaresh ◽  
SAYED MOHAMMAD REZA KHOSHROO ◽  
ROYA KARAMIAN ◽  
MOHAMMAD REZA JOHARCHI

A taxonomic review of Rhaponticoides in Iran is based on morphological characters of the specimens from the authors’ expeditions and other herbarium collections. Rhaponticoides lachnopus, R. schmidii, R. sect. Iranicae and R. sect. Ruthenicae are proposed as new combinations. Full description for the genus Rhaponticoides and R. sect. Iranicae and R. sect. Ruthenicae are presented for the first time here. Three names, R. lachnopus, R. ruthenica and its synonym, are typified. A synopsis with recognized sections and species, relevant synonyms, type citations, lists of specimens examined and an identification key are provided for the genus Rhaponticoides in Iran. In addition, some notes about ecology and habitat of Rhaponticoides especially in Iran are given. Finally, the geographical distribution of all the 4 species recognized in Iran is presented and mapped.


Zootaxa ◽  
2021 ◽  
Vol 4941 (4) ◽  
pp. 511-541
Author(s):  
GAVIN R. BROAD

The following new synonymies are established: Acrodactyla iliensis Sheng & Bian 1996 = Acrodactyla lachryma Pham, Broad, Matsumoto & Böhme 2012, syn. nov.; Euceros Gravenhorst 1829 = Lentocerus Dong & Naito 1999, syn. nov.; Euceros pruinosus (Gravenhorst 1829) = Lentocerus dentatus Dong & Naito 1999, syn. nov.; Euceros sensibus Uchida 1930 = Lentocerus lijiangensis Dong & Naito 1999, syn. nov.; Gyroneuron Kokujev 1901 = Cyclophatnus Cameron 1910, syn. nov.; Gyroneuron flavum (Cameron 1910) = Gyroneuron testaceator Watanabe 1934, syn. nov.; Liotryphon strobilellae (Linnaeus 1758) = Townesia qinghaiensis He 1996, syn. nov. The following are new combinations: Aleiodes insignis (Brues 1926), Aleiodes lateralis (Cameron 1905), Aleiodes maculicornis (Brues 1926), Aleiodes siccitesta (Morley 1937), Cyclophatnus flavum (Cameron 1910), Rhaconotus striatulus (Cameron 1909), Tolonus cingulatorius (Morley 1912), Zatypota tropica (Morley 1912). Netelia morleyi Townes, Townes & Gupta 1961 is transferred from the subgenus Netelia Gray 1860 to the subgenus Paropheltes Cameron 1907. One new replacement name is proposed: Aleiodes philippinensis nom. nov. for Rhogas lateralis Baker 1917, nec Troporhogas lateralis Cameron 1905. Lectotypes are designated for Antrusa persimilis Nixon 1954, Rhyssalus striatulus Cameron 1909, Troporhogas trimaculata Cameron 1905, Hemiteles cingulatorius Morley 1912, Paniscus ferrugineus Cameron 1889 and for Xanthojoppa inermis Morley 1917. Some previously overlooked type specimens are interpreted and illustrated and some errors in the literature corrected. Hosts are recorded for two genera of Ichneumoninae for the first time: Catadelphops nasutus (Heinrich 1962) was reared from Proserpinus terlooii (Edwards 1875) (Lepidoptera: Sphingidae) in the USA, and Aethianoplis excavata (Roman 1910) was reared from Precis octavia (Cramer 1777) (Lepidoptera: Nymphalidae) in Uganda. 


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.


1938 ◽  
Vol 4 ◽  
pp. 153-160
Author(s):  
Gustav Mayer

Marx met the then 22 years old Blind) for the first time in May 1848, when he and Engels made their appearance in the revolutionary state of Baden (Germany), after the Neue Rheinische Zeitung had been suspended. At that time they declared to the members of the republican committee at Karlsruhe (Landesa usschuss), that they considered the revolt in the South-West of Germany irretrievably doomed to failure, if no decisive moves in Hungary or another revolution in Paris should come to its rescue. The only members of the committee who supported this opinion were, as stated by Engels), Karl Blind and Amand Gögg. Soon afterwards Marx and Blind met again in Paris. On September 5 Marx gave Blind's address to Freiligrath as his own. Blind had been sent to France by the revolutionary governments of Baden and the Palatinate as one of the members of the legation, which these two shortlived republics intended to establish there. But Louis Napoleon's government ignored this legation, and consequently did not respect Blind's diplomatic immunity, when the latter, soon after his arrival, proved to be involved in the abortive coup of Ledru-Rollin of June 13. Blind was placed under arrest and expelled from France on the same day, on the ground that his presence was “such as to disturb public order and calm”.


1981 ◽  
Vol 113 (10) ◽  
pp. 907-929 ◽  
Author(s):  
Michael J. Sharkey
Keyword(s):  

AbstractNine species are recognized, of which six are new to science: Teleas crassifemur ♂, T. neptuni ♀ ♂, T. niger ♂, T. punctifrons ♀ ♂, T. terricola ♀, and T. villus ♂. The three previously described species which are retained in the genus Teleas, viz. T. lineaticeps Ashmead, T. pallidipes Ashmead and T. sibiricus Kieffer, are redescribed. Females of T. lineaticeps and T. pallidipes are described for the first time. All other Nearctic species listed by Muesebeck (1979) under Teleas are presently transferred to the genus Trimorus Foerster (subfam. Teleasinae) (all new combinations): Trimorus americanus (Ashmead), T. coxalis (Ashmead), T. harringtoni nom. nov. (= Teleas canadensis Harrington nec Acolus canadensis Ashmead), and T. mandibularis (Ashmead). T. sibiricus Kieffer is the only member of the genus known to have Holarctic distribution.A key to the females and males of Nearctic Teleas and a key to Nearctic genera of Teleasinae are presented.


2019 ◽  
Vol 64 (2) ◽  
pp. 345-366
Author(s):  
Mikhail P. Zhurbenko ◽  
Ochirbat Enkhtuya ◽  
Samiya Javkhlan

AbstractA first synopsis of lichenicolous fungi of Mongolia based on new collections and literature data is provided, including 114 species. Five new species are described: Capronia cogtii (on Vahliella leucophaea), Echinothecium hypogymniae (on Hypogymnia bitteri), Feltgeniomyces mongolicus (on H. bitteri), Phacopsis vulpicidae (on Vulpicida juniperina) and Roselliniella javkhlanae (on Rinodina turfacea var. ecrustacea). Two new combinations are proposed: Endococcus hafellneri (≡ Stigmidium hafellneri) and Sphaerellothecium taimyricum (≡ Sphaerellothecium thamnoliae var. taimyricum). Unidentified specimens of Acremonium (on Mycoblastus sanguinarioides), Cercidospora (on Rhizoplaca chrysoleuca s.lat.), Didymocyrtis (on Rhizoplaca chrysoleuca s.lat.), Lichenochora (on Physcia alnophila), Lichenostigma (on species of Xanthoparmelia), Phoma (on Vulpicida juniperina) and a leotialean fungus (on Cetraria laevigata) are characterized and discussed. Taxonomic notes are provided for Cercidospora macrospora s.lat., Didymocyrtis cf. melanelixiae, Minutoexcipula cf. beaglei, Nesolechia cetrariicola, Sphaerellothecium cf. parmeliae and Stigmidium cf. psorae. Sphaeropezia intermedia is newly reported for Eurasia. Didymocyrtis grumantiana is newly reported for Asia. Additionally, 71 species of lichenicolous fungi and five species of lichenicolous lichens are documented in Mongolia for the first time. Allocetraria is reported as a new host genus for Abrothallus peyritschii, Vulpicida for Arthonia triebeliae, and Anamylopsora for Muellerella pygmaea.


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