Fungal systematics and evolution最新文献

{"title":"Phylogenetic placement and reassessment of <i>Asperisporium pongamiae</i> as <i>Pedrocrousiella pongamiae gen. et comb. nov.</i> (<i>Mycosphaerellaceae</i>).","authors":"K C Rajeshkumar,&nbsp;U Braun,&nbsp;J Z Groenewald,&nbsp;S S Lad,&nbsp;N Ashtekar,&nbsp;S Fatima,&nbsp;G Anand","doi":"10.3114/fuse.2021.07.08","DOIUrl":"https://doi.org/10.3114/fuse.2021.07.08","url":null,"abstract":"<p><p>The leaf spot disease of <i>Pongamia pinnata</i> caused by an asperisporium-like asexual morph, which is usually referred to as <i>Asperisporium pongamiae</i>, is quite common during monsoon seasons in India. Phylogenetic analyses, based on LSU and <i>rpb2</i> sequence data, and blast searches using ITS sequence data, revealed that this ascomycete forms a lineage within <i>Mycosphaerellaceae</i> distant from all other generic lineages. <i>Pedrocrousiella gen. nov.</i>, with <i>P. pongamiae comb. nov.</i>, based on <i>Fusicladium pongamiae</i> (≡ <i>A. pongamiae</i>), as type species is introduced for this lineage. This species has been considered the asexual morph of <i>Mycosphaerella pongamiae</i> (≡ <i>Stigmatea pongamiae</i>). However, this connection is unproven and was just based on the occasional association of the two taxa in some collections. Several attempts to induce the formation of a sexual morph in culture failed, therefore the putative connection between these morphs could not be confirmed. <i>Asperisporium pongamiae</i>-<i>pinnatae</i> is reduced to synonymy with <i>P. pongamiae</i>. <i>Asperisporium pongamiae</i>-<i>pinnatae</i> was introduced because of the wrong assumption that <i>F. pongamiae</i> had been described on another host, <i>Pongamia globosa</i>. But <i>Fusicladium pongamiae</i> was actually described in India on <i>Pongamia glabra</i>, which is a synonym of <i>P. pinnata</i>, and hence on the same host as <i>Asperisporium pongamiae-pinnatae</i>. <i>Pedrocrousiella pongamiae</i> clusters in a clade containing <i>Distocercospora</i>, <i>Clypeosphaerella</i>, and \"<i>Pseudocercospora</i>\" <i>nephrolepidicola</i>, a species which is not congeneric with <i>Pseudocercospora</i>. Phylogenetically, <i>Pedrocrousiella</i> is distant from the <i>Asperisporium s. str.</i> clade (type species <i>A. caricae</i>), which is more closely related to <i>Amycosphaerella</i>, <i>Pseudocercosporella</i>, <i>Distomycovellosiella</i> and <i>Nothopassalora</i>. <b>Citation:</b> Rajeshkumar KC, Braun U, Groenewald JZ, Lad SS, Ashtekar N, Fatima S, Anand G (2021). Phylogenetic placement and reassessment of <i>Asperisporium pongamiae</i> as <i>Pedrocrousiella pongamiae gen. et comb. nov.</i> (<i>Mycosphaerellaceae</i>). <i>Fungal Systematics and Evolution</i> <b>7:</b> 165-176. doi: 10.3114/fuse.2021.07.08.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d3/36/fuse-2021-7-8.PMC8166208.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39024001","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"<i>Sirolpidium bryopsidis</i>, a parasite of green algae, is probably conspecific with <i>Pontisma lagenidioides</i>, a parasite of red algae.","authors":"A T Buaya,&nbsp;B Scholz,&nbsp;M Thines","doi":"10.3114/fuse.2021.07.11","DOIUrl":"https://doi.org/10.3114/fuse.2021.07.11","url":null,"abstract":"<p><p>The genus <i>Sirolpidium</i> (<i>Sirolpidiaceae</i>) of the <i>Oomycota</i> includes several species of holocarpic obligate aquatic parasites. These organisms are widely occurring in marine and freshwater habitats, mostly infecting filamentous green algae. Presently, all species are only known from their morphology and descriptive life cycle traits. None of the seven species classified in <i>Sirolpidium,</i> including the type species, <i>S. bryopsidis,</i> has been rediscovered and studied for their molecular phylogeny, so far. Originally, the genus was established to accommodate all parasites of filamentous marine green algae. In the past few decades, however, <i>Sirolpidium</i> has undergone multiple taxonomic revisions and several species parasitic in other host groups were added to the genus. While the phylogeny of the marine rhodophyte- and phaeophyte-infecting genera <i>Pontisma</i> and <i>Eurychasma</i>, respectively, has only been resolved recently, the taxonomic placement of the chlorophyte-infecting genus <i>Sirolpidium</i> remained unresolved. In the present study, we report the phylogenetic placement of <i>Sirolpidium bryopsidis</i> infecting the filamentous marine green algae <i>Capsosiphon fulvescens</i> sampled from Skagaströnd in Northwest Iceland. Phylogenetic reconstructions revealed that <i>S. bryopsidis</i> is either conspecific or at least very closely related to the type species of <i>Pontisma</i>, <i>Po. lagenidioides</i>. Consequently, the type species of genus <i>Sirolpidium</i>, <i>S. bryopsidis</i>, is reclassified to <i>Pontisma</i>. Further infection trials are needed to determine if <i>Po. bryopsidis</i> and <i>Po. lagenidioides</i> are conspecific or closely related. In either case, the apparently recent host jump from red to green algae is remarkable, as it opens the possibility for radiation in a largely divergent eukaryotic lineage. <b>Citation:</b> Buaya AT, Scholz B, Thines M (2021). <i>Sirolpidium bryopsidis</i>, a parasite of green algae, is probably conspecific with <i>Pontisma lagenidioides</i>, a parasite of red algae. <i>Fungal Systematics and Evolution</i> <b>7:</b> 223-231. doi: 10.3114/fuse.2021.07.11.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/6e/1b/fuse-2021-7-11.PMC8165961.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39024004","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Four new species of <i>Hydnellum</i> (<i>Thelephorales</i>, <i>Basidiomycota</i>) with a note on <i>Sarcodon illudens</i>.","authors":"J Nitare, A M Ainsworth, E Larsson, D Parfitt, L M Suz, S Svantesson, K-H Larsson","doi":"10.3114/fuse.2021.07.12","DOIUrl":"10.3114/fuse.2021.07.12","url":null,"abstract":"<p><p>Four new <i>Hydnellum</i> species are described. <i>Hydnellum roseoviolaceum sp. nov</i>. grows in dry pine heaths on acidic, sandy soil. It is close to <i>H. fuligineoviolaceum</i>, another pine-associated species, but differs by smaller spores, an initially rose-coloured instead of violet flesh in fresh basidiomata and a mild taste. <i>Hydnellum scabrosellum sp. nov</i>. grows in coniferous forests on calcareous soil. It shares a general morphology with <i>H. scabrosum</i>, which also is its closest relative. It differs by having smaller and slenderer basidiomata and by the yellowish ochraceous colour of flesh and spines in dried specimens compared to the whitish or reddish brown colour seen in <i>H. scabrosum</i>. <i>Hydnellum fagiscabrosum sp. nov</i>. is another species with morphological and phylogenetic affinities to <i>H. scabrosum</i>. However, it is associated with trees from <i>Fagales</i> whereas <i>H. scabrosum</i> is associated with <i>Pinaceae</i>. <i>Hydnellum nemorosum sp. nov</i>. is yet another species that associates with broadleaved trees. It seems to be a rare species, morphologically reminiscent of <i>H. fuligineoviolaceum</i>, <i>H. ioeides</i> and <i>H. scabrosum,</i> but it is phylogenetically close to <i>H. fennicum</i>. Sequences from the type specimens of <i>H. glaucopus</i>, <i>H. lepidum</i>, <i>H. scabrosum</i>, <i>Sarcodon illudens</i> and <i>S. regalis</i> are included in the analyses. Specimens given the provisional name \"<i>Sarcodon pseudoglaucopus</i>\" in Sweden are now shown to be referable to <i>S. illudens</i>. The analyses further showed that <i>S. illudens</i> is close to <i>H. lepidum</i>. The new combination <i>Hydnellum illudens</i> is proposed. <i>Sarcodon regalis</i> and <i>H</i>. <i>lepidum</i> are shown to be conspecific and, although their basionyms were simultaneously published, the name <i>S. regalis</i> was only validated in a later publication. <i>Hydnellum lepidum</i> therefore takes priority and <i>S. regalis</i> becomes a synonym. <b>Citation:</b> Nitare J, Ainsworth AM, Larsson E, Parfitt D, Suz LM, Svantesson S, Larsson K-H (2021). Four new species of <i>Hydnellum</i> (<i>Thelephorales</i>, <i>Basidiomycota</i>) with a note on <i>Sarcodon illudens</i>. <i>Fungal Systematics and Evolution</i> <b>7:</b> 233-254. doi: 10.3114/fuse.2021.07.12.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/04/85/fuse-2021-7-12.PMC8165966.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39024005","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Phylogenetic delimitation of <i>Apiospora</i> and <i>Arthrinium</i>.","authors":"Á Pintos,&nbsp;P Alvarado","doi":"10.3114/fuse.2021.07.10","DOIUrl":"https://doi.org/10.3114/fuse.2021.07.10","url":null,"abstract":"<p><p>In the present study six species of <i>Arthrinium</i> (including a new taxon, <i>Ar. crenatum</i>) are described and subjected to phylogenetic analysis. The analysis of ITS and 28S rDNA, as well as sequences of <i>tef1</i> and <i>tub2</i> exons suggests that <i>Arthrinium s. str.</i> and <i>Apiospora</i> represent independent lineages within <i>Apiosporaceae</i>. Morphologically, <i>Arthrinium</i> and <i>Apiospora</i> do not seem to have clear diagnostic features, although species of <i>Arthrinium</i> often produce variously shaped conidia (navicular, fusoid, curved, polygonal, rounded), while most species of <i>Apiospora</i> have rounded (face view) / lenticular (side view) conidia. Ecologically, most sequenced collections of <i>Arthrinium</i> were found on <i>Cyperaceae</i> or <i>Juncaceae</i> in temperate, cold or alpine habitats, while those of <i>Apiospora</i> were collected mainly on <i>Poaceae</i> (but also many other plant host families) in a wide range of habitats, including tropical and subtropical regions. A lectotype for <i>Sphaeria apiospora</i> (syn.: <i>Ap. montagnei</i>, type species of <i>Apiospora</i>) is selected among the original collections preserved at the PC fungarium, and the putative identity of this taxon, found on <i>Poaceae</i> in Mediterranean lowland habitats, is discussed. Fifty-five species of <i>Arthrinium</i> are combined to <i>Apiospora</i>, and a key to species of <i>Arthrinium s. str.</i> is provided. <b>Citation:</b> Pintos Á, Alvarado P (2021). Phylogenetic delimitation of <i>Apiospora</i> and <i>Arthrinium</i>. <i>Fungal Systematics and Evolution</i> <b>7:</b> 197-221. doi: 10.3114/fuse.2021.07.10.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/25/68/fuse-2021-7-10.PMC8165962.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39024003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Taxonomy and phylogeny of the basidiomycetous hyphomycete genus <i>Hormomyces</i>.","authors":"J Mack, R A Assabgui, K A Seifert","doi":"10.3114/fuse.2021.07.09","DOIUrl":"10.3114/fuse.2021.07.09","url":null,"abstract":"<p><p>The taxonomy of the genus <i>Hormomyces</i>, typified by <i>Hormomyces aurantiacus,</i> which based on circumstantial evidence was long assumed to be the hyphomycetous asexual morph of <i>Tremella mesenterica</i> (<i>Tremellales</i>, <i>Tremellomycetes</i>) or occasionally <i>Dacrymyces</i> (<i>Dacrymycetales</i>, <i>Dacrymycetes</i>)<i>,</i> is revised. Phylogenies based on the three nuc rDNA markers [internal transcribed spacers (ITS), 28S large ribosomal subunit nrDNA (28S) and 18S small ribosomal subunit nrDNA (18S)], based on cultures from Canada and the United States, suggest that the genus is synonymous with <i>Tulasnella</i> (<i>Cantharellales</i>, <i>Agaricomycetes</i>) rather than <i>Tremella</i> or <i>Dacrymyces.</i> Morphological studies of 38 fungarium specimens of <i>Hormomyces</i>, including the type specimens of <i>H. callorioides</i>, <i>H. fragiformis</i>, <i>H. paridiphilus</i> and <i>H. peniophorae</i> and examination of the protologues of <i>H. abieticola</i>, <i>H. aurantiacus</i> and <i>H. pezizoideus</i> suggest that <i>H. callorioides</i> and <i>H. fragiformis</i> are conspecific with <i>H. aurantiacus</i> while the remaining species are unlikely to be related to <i>Tulasnella</i>. The conidial chains produced by <i>H. aurantiacus</i> are similar to monilioid cells of asexual morphs of <i>Tulasnella</i> species formerly referred to the genus <i>Epulorhiza</i>. The new combination <i>Tulasnella aurantiaca</i> is proposed and the species is redescribed, illustrated and compared with similar fungi. The ecological niche of <i>T. aurantiaca</i> and its possible relationship to orchid root endophytes is discussed. A key to asexual genera with similar conidium ontogeny to <i>T. aurantiaca</i> is provided. <b>Citation:</b> Mack J, Assabgui RA, Seifert KA (2021). Taxonomy and phylogeny of the basidiomycetous hyphomycete genus <i>Hormomyces</i>. <i>Fungal Systematics and Evolution</i> <b>7:</b> 177-196. doi: 10.3114/fuse.2021.07.09.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/80/39/fuse-2021-7-9.PMC8166209.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39024002","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"New and Interesting Fungi. 4.","authors":"P W Crous, M Hernández-Restrepo, R K Schumacher, D A Cowan, G Maggs-Kölling, E Marais, M J Wingfield, N Yilmaz, O C G Adan, A Akulov, E Álvarez Duarte, A Berraf-Tebbal, T S Bulgakov, A J Carnegie, Z W de Beer, C Decock, J Dijksterhuis, T A Duong, A Eichmeier, L T Hien, J A M P Houbraken, T N Khanh, N V Liem, L Lombard, F M Lutzoni, J M Miadlikowska, W J Nel, I G Pascoe, F Roets, J Roux, R A Samson, M Shen, M Spetik, R Thangavel, H M Thanh, L D Thao, E J van Nieuwenhuijzen, J Q Zhang, Y Zhang, L L Zhao, J Z Groenewald","doi":"10.3114/fuse.2021.07.13","DOIUrl":"10.3114/fuse.2021.07.13","url":null,"abstract":"<p><p>An order, family and genus are validated, seven new genera, 35 new species, two new combinations, two epitypes, two lectotypes, and 17 interesting new host and / or geographical records are introduced in this study. Validated order, family and genus: <i>Superstratomycetales</i> and <i>Superstratomycetaceae</i> (based on <i>Superstratomyces</i> <i>)</i>. New genera: <i>Haudseptoria</i> (based on <i>Haudseptoria typhae</i>); <i>Hogelandia</i> (based on <i>Hogelandia lambearum</i>); <i>Neoscirrhia</i> (based on <i>Neoscirrhia osmundae</i>); <i>Nothoanungitopsis</i> (based on <i>Nothoanungitopsis urophyllae</i>); <i>Nothomicrosphaeropsis</i> (based on <i>Nothomicrosphaeropsis welwitschiae</i>); <i>Populomyces</i> (based on <i>Populomyces zwinianus</i>); <i>Pseudoacrospermum</i> (based on <i>Pseudoacrospermum goniomae</i>). New species: <i>Apiospora sasae</i> on dead culms of <i>Sasa veitchii</i> (Netherlands); <i>Apiospora stipae</i> on dead culms of <i>Stipa gigantea</i> (Spain); <i>Bagadiella eucalyptorum</i> on leaves of <i>Eucalyptus</i> sp. (Australia); <i>Calonectria singaporensis</i> from submerged leaf litter (Singapore); <i>Castanediella neomalaysiana</i> on leaves of <i>Eucalyptus</i> sp. (Malaysia); <i>Colletotrichum pleopeltidis</i> on leaves of <i>Pleopeltis</i> sp. (South Africa); <i>Coniochaeta deborreae</i> from soil (Netherlands); <i>Diaporthe durionigena</i> on branches of <i>Durio zibethinus</i> (Vietnam); <i>Floricola juncicola</i> on dead culm of <i>Juncus</i> sp. (France); <i>Haudseptoria typhae</i> on leaf sheath of <i>Typha</i> sp. (Germany); <i>Hogelandia lambearum</i> from soil (Netherlands); <i>Lomentospora valparaisensis</i> from soil (Chile); <i>Neofusicoccum mystacidii</i> on dead stems of <i>Mystacidium capense</i> (South Africa); <i>Neomycosphaerella guibourtiae</i> on leaves of <i>Guibourtia</i> sp. (Angola); <i>Niesslia neoexosporioides</i> on dead leaves of <i>Carex paniculata</i> (Germany); <i>Nothoanungitopsis urophyllae</i> on seed capsules of <i>Eucalyptus urophylla</i> (South Africa); <i>Nothomicrosphaeropsis welwitschiae</i> on dead leaves of <i>Welwitschia mirabilis</i> (Namibia); <i>Paracremonium bendijkiorum</i> from soil (Netherlands); <i>Paraphoma ledniceana</i> on dead wood of <i>Buxus sempervirens</i> (Czech Republic); <i>Paraphoma salicis</i> on leaves of <i>Salix cf. alba</i> (Ukraine); <i>Parasarocladium wereldwijsianum</i> from soil (Netherlands); <i>Peziza ligni</i> on masonry and plastering (France); <i>Phyllosticta phoenicis</i> on leaves of <i>Phoenix reclinata</i> (South Africa); <i>Plectosphaerella slobbergiarum</i> from soil (Netherlands); <i>Populomyces zwinianus</i> from soil (Netherlands); <i>Pseudoacrospermum goniomae</i> on leaves of <i>Gonioma kamassi</i> (South Africa); <i>Pseudopyricularia festucae</i> on leaves of <i>Festuca californica</i> (USA); <i>Sarocladium sasijaorum</i> from soil (Netherlands); <i>Sporothrix hypoxyli</i> in sporocarp of <i>Hypoxylon petriniae</i> on <i>F","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/07/aa/fuse-2021-7-13.PMC8165967.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39024007","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Eight new <i>Elaphomyces</i> species (<i>Elaphomycetaceae, Eurotiales, Ascomycota</i>) from eastern North America.","authors":"M A Castellano,&nbsp;C D Crabtree,&nbsp;D Mitchell,&nbsp;R A Healy","doi":"10.3114/fuse.2021.07.06","DOIUrl":"https://doi.org/10.3114/fuse.2021.07.06","url":null,"abstract":"<p><p>The hypogeous, sequestrate ascomycete genus <i>Elaphomyces</i> is one of the oldest known truffle-like genera. <i>Elaphomyces</i> has a long history of consumption by animals in Europe and was formally described by Nees von Esenbeck in 1820 from Europe. Until recently most <i>Elaphomyces</i> specimens in North America were assigned names of European taxa due to lack of specialists working on this group and difficulty of using pre-modern species descriptions. It has recently been discovered that North America has a rich diversity of <i>Elaphomyces</i> species far beyond the four <i>Elaphomyces</i> species described from North America prior to 2012. We describe eight new <i>Elaphomyces</i> species (<i>E. dalemurphyi, E. dunlapii, E. holtsii</i>, <i>E. lougehrigii</i>, <i>E. miketroutii</i>, <i>E. roody</i>i, <i>E. stevemilleri</i> and <i>E. wazhazhensis</i>) of eastern North America that were collected in habitats from Quebec, Canada south to Florida, USA, west to Texas and Iowa. The ranges of these species vary and with continued sampling may prove to be larger than we have established. Castellano has studied authentic material of all European <i>Elaphomyces</i> species published through 2016 and it is interesting to note that many <i>Elaphomyces</i> species from eastern North America have morphological similarities but with distinct morphological differences to a number of European <i>Elaphomyces</i> species. <b>Citation:</b> Castellano MA, Crabtree CD, Mitchell D, Healy RA (2020). Eight new <i>Elaphomyces</i> species (<i>Elaphomycetaceae</i>, <i>Eurotiales</i>, <i>Ascomycota</i>) from eastern North America. <i>Fungal Systematics and Evolution</i> <b>7:</b> 113-131. doi: 10.3114/fuse.2021.07.06.</p>","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/21/b4/fuse-2021-7-6.PMC8166207.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39011758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Figure S1","authors":"N. Davoodian","doi":"10.3114/fuse.2021.08.06_supp1","DOIUrl":"https://doi.org/10.3114/fuse.2021.08.06_supp1","url":null,"abstract":"Fig. S1. Overview Phylogram from Bayesian analysis showing relationship between Hysterangiales, some Phallales and outgroups (OG). Node A indicates Phallogastrineae subord. nov.; node B indicates Hysterangineae subord. nov. Maximum likelihood (ML) bootstrap values / Bayesian posterior probabilities (bpp) are shown at the nodes. Where bpp ≥ 0.95 and ML bootstrap ≥ 70 %, branches are thickened. Type species indicated by a blue asterisk *. The asterisk in parentheses (*) denotes the currently accepted genus for Protubera canescens, Ileodictyon. Countries and States indicated with same acronyms as Fig. 3. Terminals representing new DNA sequences generated for this study are in bold.","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"82327371","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Fig. S1 & Tables S1-S4","authors":"E. De Crop","doi":"10.3114/fuse.2021.07.07_supp1","DOIUrl":"https://doi.org/10.3114/fuse.2021.07.07_supp1","url":null,"abstract":"Figure S1. Overview map of the biogeographical regions used for Table 1. Biogeographic regions are based on biogeographic realms (https://ecoregions2017.appspot.com/), with three major differences: Western Palearctic (Western part of the Palearctic realm), Asia (Eastern part of the Palearctic realm combined with the Indo-Malay realm), and Australasia (Australasian realm combined with the Oceanian realm). The Palearctic realm was spilt into Western Palearctic and Eastern Palearctic, Eastern Palearctic and the Indo-Malay realm form together the Asia region, and the Australasian realm is combined with the Oceania realm to form the Australasian region.Table S1. List of described Lactifluus species, together with the year of description, taxonomical classification (subgenus, section), the indication of how this taxonomical position was defined, the source(s) of this classification, and notes.Table S2. Extra information on the preliminary study of metabarcoding data of the genus Lactifluus, retrieved from the GlobalFungi website.Table S3. Overview of the results of the preliminary study of metabarcoding data of the genus Lactifluus, retrieved from the GlobalFungi website. Due to the generally shorter length and lower quality of environmental sequence data, the numbers in the table are to be considered an estimate.Table S4. List of the putative new species found in the environmental sequences. References of studies cited are given in S3.","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73085692","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Figs S1-S4 & Table S1","authors":"J. Mack","doi":"10.3114/fuse.2021.07.09_supp1","DOIUrl":"https://doi.org/10.3114/fuse.2021.07.09_supp1","url":null,"abstract":"Figure S1. Mean conidial dimensions (with error bars representing standard error) for all herbarium specimens and cultures examined, with the holotype of H. fragiforme represented by orange bars and the holotype of H. callorioides represented by green bars.Figure S2. Lectotype of H. fragiformis (A, C, E) and holotype of H. callorioides (B, D, F). A, B. Rehydrated sporodochia. C−F. Conidial chains. Scale bars: A, B = 500 μm. C−F = 10 μm.Figure S3. Conidia and conidial chains. A. Oosporidium sp. (DAOM 970823) identified using DNA sequencing. B. Holotype of Sphaerocolla aurantiaca (H). Both have similar conidial morphology and dimensions, suggesting that S. aurantiaca may be conspecific with Oosporidium margaritiferum. Scale bar = 10 μm. Figure S4. Nuclear staining of hyphae of DAOMC 251988, showing dikaryotic, binucleate hyphae, A, using near-UV light showing the stained nuclei and B with regular light. Scale bar = 20 μm. Table S1. Species, geographical location, host and herbaria for known type specimens of Hormomyces species.","PeriodicalId":73121,"journal":{"name":"Fungal systematics and evolution","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88013398","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}