Fungi of Bulgaria. Vol. 8. Diaporthales

Total Page:16

File Type:pdf, Size:1020Kb

Fungi of Bulgaria. Vol. 8. Diaporthales FUNGI OF BULGARIA. VOL. 8. DIAPORTHALES Dimitar Y. Stoykov Institute of Biodiversity and Ecosystem Research, Bulgarian Academy of Sciences 23, Acad. G. Bonchev Str., BG-1113, Sofia, Bulgaria e-mail address: [email protected] The current volume is a result of many years of studies on the fungal diversity, taxonomy, distribution and economic importance of Diaporthales in Bulgaria. This work is an attempt to present systematically the knowledge of those fungal group for the first time in our country. Data about order Diaporthales, includind five families, 31 genera, and 104 species are included. Diaporthalean fungi are reported on 94 species of higher plants (grasses, shrubs and trees) from 46 genera, which are referred to 22 plant families. General information on seasonal development and vertical distribution of the fungi throughout the country is presented also. The text is supplemented with 82 fine line drawings made from original microscope slides using drawing facilities under LM and a technique described in Stoykov & Assyov (2009). This book includes a general part dealing with the principles of classification, taxonomically significant characters, brief reviews on the studies of Diaporthales worldwide and taxonomic concepts about these fungi, their economic importance, where known. A special part, incuding keys for determination of families, genera and species; brief descriptions of the taxa, bearing basic statistic information about the ascospores’ length and width measures, l/w ratio, distribution in Bulgaria and data about their known general distribution throghout the world, as lists of the hosts/substrata so far known in the country. Brief notes on variability on some species is included also. Most of the specimens examined are kept at the Mycological Collection (SOMF), Institute of Biodiversity and Ecosystem Research, Bulgarian Academy of Sciences. Part of the studies, held during 2008 in the Royal Botanic Gardens, Kew (UK), were financed by SYNTHESYS project GB-TAF-3824 “Taxonomy of Diaporthales (Ascomycota) in Bulgaria” and the politely cooperation of the Department of Mycology, Jodrell laboratory, RBG (Kew). LIST OF ALL TAXA1 ASCOMYCOTA Caval.-Sm. Pezizomycotina O.E. Erikss. & Winka Sordariomycetes sensu O.E. Erikss. & Winka Sordariomycetidae O.E. Erikss. & Winka Diaporthales Nannf. Cryphonectriaceae Gryzenh. & M.J. Wingf. 1. Cryphonectria (Sacc.) Sacc. & D. Sacc. 1( 1). Cryphonectria parasitica (T.J. Murray) M.E. Barr Diaporthaceae Höhn. ex Wehm. 2. Allantoporthe Petr. 1( 2). Allantoporthe tessella (Pers. : Fr.) Petr. 3. Apioporthella Petr. 1( 3). Apioporthella vepris (Delacr.) M.E. Barr 4. Diaporthe Nitschke 1( 4). Diaporthe angelicae (Berk.) Farr & Castleb. 2( 5). D. carpini (Pers.) Fuckel 3( 6). D. crataegi (Curr.) Nitschke 4( 7). D. eres Nitschke 5( 8). D. fagi Wehm. 6( 9). D. fibrosa (Pers. : Fr.) Fuckel 7(10). D. helianthi Munt.-Cvetk., Mihaljč. & M. Petrov 8(11). D. juglandina (Fuckel) Nitschke 9(12). D. leiphaemia (Fr. : Fr.) Sacc. *D. linearis (Nees : Fr.) Nitschke 10(13). D. oncostoma (Duby) Fuckel 11(14). D. perniciosa Marchal & É.J. Marchal *D. phaseolorum (Cooke & Ellis) Sacc. 12(15). D. pustulata (Desm.) Sacc. Gnomoniaceae G. Winter 5. Apiognomonia Höhn. 1(16). Apiognomonia acerina (Starbäck) M. Monod 2(17). A. errabunda (Robergе ex Desm.) Höhn. 3(18). A. erythrostoma (Pers. : Fr.) Höhn. 4(19). A. fakirovae Stoykov 5(20). A. petiolicola (Fuckel) M. Monod 6(21). A. veneta (Sacc. & Speg.) Höhn. 6. Cryptodiaporthe Petr. *Cryptodiaporthe aesculi (Fuckel) Petr. 1(22). C. apiculata (Wallr.) Petr. *C. castanea (Tul. & C. Tul.) Wehm. 2(23). C. populea (Sacc.) Butin ex Butin 3(24). C. salicella (Fr. : Fr.) Petr. 1Species possibly to occur in Bulgaria are marked with an asrterisk (*) 7. Cryptosporella Sacc. 1(25). Cryptosporella betulae (Tul. & C. Tul.) L.C. Mejía & Castleb. 2(26). C. suffusa (Fr. : Fr.) L.C. Mejía & Castleb. 8. Diaporthella Petr. 3(27). Diaporthella aristata (Fr. : Fr.) Petr. 9. Ditopella J. Schröt. 4(28). Ditopella ditopa (Fr. : Fr.) J. Schröt. 10. Gnomonia Ces. & De Not. 5(29). Gnomonia alnea (Fr. : Fr.) Sogonov *G. alpina (G. Winter) G. Winter 6(30). G. arnstadtiensis Auersw. 7(31). G. amoena (Nees : Fr.) Ces. & De Not. 8(32). G. betulina Vleugel 9(33). G. carpinicola (Höhn.) Sogonov 10 (34). G. cerastis (Riess) Ces. & De Not. *G. dryadis Auersw. 11(35). G. gei Pat. & Doass. 12(36). G. geranii-macrorrhizi Fakirova 13(37). G. gnomon (Tode : Fr.) J. Schröt. 14(38). G. ischnostyla (Desm.) Auersw. 15(39). G. orientalis M. Monod 16(40). G. ostryae De Not. 17(41). G. pruni Fuckel 18(42). G. pseudoamoena M. Monod 19(43). G. rostellata (Fr. : Fr.) Wehm. *G. sanguisorbae (Rehm) E. Müll. 20(44). G. tetraspora G. Winter 21(45). G. vallesiaca M. Monod 11. Gnomoniella Sacc. 1(46). Gnomoniella tubaeformis (Tode : Fr.) Sacc. 12. Gnomoniopsis Berl. 1(47). Gnomoniopsis comari (P. Karst.) Sogonov, s. lat. 13. Linospora Fuckel 1(48). Linospora capreae (DC. : Fr.) Fuckel 14. Mamiania Ces. & De Not. 1(49). Mamiania fimbriata (Pers. : Fr.) Ces. & De Not. 15. Mamianiella Höhn. 1(50). Mamianiella coryli (Batsch : Fr.) Höhn. 16. Ophiognomonia (Sacc.) Sacc. 1(51). Ophiognomonia alni-viridis (Podl.-Růž. & Svrček) Sogonov 2(52). O. gei-montani (Ranoj.) Sogonov 3(53). O. leptostyla (Fr. : Fr.) Ces. & De Not. *O. melanostyla (DC. : Fr.) Sacc. ex Berl. 4(54). O. rosae (Fuckel) Sogonov 5(55). O. setacea (Pers. : Fr.) Sogonov 17. Plagiosphaera Petr. 1(56). Plagiosphaera immersa (Trail) Petr. 18. Plagiostoma Fuckel *Plagiostoma aesculi (Fuckel) Sogonov 1(57). P. amygdalinae (Fuckel) Sogonov 2(58). P. bavaricum (Rehm) M. E. Barr 3(59). P. castanicolum Fakirova 4(60). P. devexum (Desm.) Fuckel 5(61). P. geranii (Hollós) Sogonov 6(62). P. inclinatum (Desm.) M. E. Barr 19. Pleuroceras Riess 1(63). Pleuroceras pleurostylum (Auersw.) M. E. Barr Сем. Melanconidaceae G. Winter 20. Apiosporopsis Fabre 1(64). Apiosporopsis carpinea (Fr. : Fr.) Mariani 21. Melanconis Tul. & C. Tul. 1(65). Melanconis aucta (Berk. & Brоome) Wehm. 2(66). M. chrysostroma (Fr. : Fr.) Tul. & C. Tul. 3(67). M. juglandis (Ellis & Everh.) A.H. Graves 4(68). M. modonia Tul. & C. Tul. 5(69). M. stilbostroma (Fr. : Fr.) Tul. & C. Tul. *M. thelebola (Fr. : Fr.) Sacc. 22. Melogramma Fr. 1(70). Melogramma spiniferum (Wallr.) De Not. 23. Pseudovalsa Höhn. 1(71). Pseudovalsa lanciformis (Fr. : Fr.) Ces. & De Not. 2(72). P. umbonata (Tul. & C. Tul.) Sacc. 24. Sydowiella Petr. 1(73). Sydowiella depressula (P. Karst.) M. E. Barr 2(74). S. fenestrans (Duby) Petr. Valsaceae Tul. & C. Tul. 25. Apioplagiostoma M.E. Barr 1(75). Apioplagiostoma aceriferum (Cooke) M.E. Barr 26. Ditopellina J. Reid & C. Booth 1(76). Ditopellina saccardoana (Traverso & Spessa) J. Reid & C. Booth 27. Hypospilina (Sacc.) Traverso 1(77). Hypospilina bifrons (Kunze & J.C. Schmidt : Fr.) Traverso 2(78). H. pustula (Pers. : Fr.) M. Monod 28. Leucostoma (Nitschke) Höhn. 1(79). Leucostoma auerswaldii (Nitschke) Höhn. 2(80). L. cinctum (Fr. : Fr.) Fr. 3(81). L. massarianum (De Not.) Höhn. 4(82). L. niveum (Hoffm. : Fr.) Höhn. 5(83). L. personii (Nitschke) Höhn. 6(84). L. translucens (De Not.) Höhn. 29. Sillia P. Karst. 1(85). Sillia ferruginea (Pers. : Fr.) P. Karst. 30. Valsa Fr. Sect. Cypri Z. Urb. 1(86). Valsa cypri (Tul.) Tul. & C. Tul. Sect. Monostichae Nitschke 2(87). V. ceratosperma (Tode : Fr.) Maire Sect. Valsa 3(88). V. ambiens (Pers. : Fr.) Fr. 4(89). V. betulina Nitschke 5(90). V. fallax Nitschke 6(91). V. intermedia Nitschke 7(92). V. salicina (Pers. : Fr.) Fr. 8(93). V. sordida Nitschke 9(94). V. viburni Fuckel 31. Valsella Fuckel 1(95). Valsella nigroannulata Fuckel Gnomonia geranii-macrorrhizi Fakirova, Mycotaxon, 54: 329, 1995. (english summary) Ascomata (280) 380-515 (560) μm in diam, black, globose to depressed globose; immersed in the tissues of the stems and petioles. Necks (320) 370-490 (750) × (50) 55-85 (100) μm, straight, slightly widened at the base, central. Asci (63.5) 70-100 (110) × (11) 13- 16.5 (20) μm, fusoid, numerous, 8-spored, with biseriately overlapping ascospores and conspicuous apical annulus ca 4 μm. Spores (20) 25.2±2.8 (35) × (4.5) 5.9±0.6 (7.5) μm, n = 450, l/w (3.1–5.5), hyaline, straight, broad ellipsoid; with median septum, not constricted at septum; ends obtuse, with broad spathuliform, hyaline appendage at both ends, 3-3.3 × 2-2.5 μm. Each cell with 2 large guttules. Conidial state: unknown. Distribution: On overwintered or dry petioles of Geranium macrorrhizum L. – Eastern Forebalkan (Golyama Zhelyazna and Patreshko villages; Vrachanski Balkan Natural Park, above Ledenika chalet, near the road to Kravya locality), Sofia region (Sofia, Akademika Stadium; Vrana Park), Vitosha region (Bistritsa; Simeonovo; near Boyanski Waterfall; Mt. Lyulin), Mt. Belasitsa (Samouilovo; above Skrut); Mt. Slavyanka (Ali Botush Reserve, Hambar Dere locality), Pirin Mts (Vihren chalet), Sredna Gora Mts (Lozenska Planina, Pancharevo dam-lake; Dolni Pasarel, Rakita river; Novi Han), the Rhodopes (Shiroka Polyana locality). Gnomonia geranii-macrorrhizi, asci and spores in water, Sofia region, Vrana Park (D. Stoykov, personal photo, April 2018) Plagiostoma castanicolum Fakirova, Int. J. Mycol. Lichenol., 5(3): 209, 1992 (english summary) Ascomata (180) 280-420 × 250-310 (350) μm, light-brownish to black, ob-lique or horizontally depressed, single or in groups, immersed in leaves. Necks (50) 70-170 (350) × 40-70 (100) μm, periphysate, ± projecting through the surface of the leaf, straight or slightly curved, broadened near the base, lateral and visible from the upper leaf side. Asci 50–70 (85) × (7) 8–11 μm, fusoid, 8–spored, with biseriate ascospores and apical annulus 3-3.5 μm. Ascospores (12.5) 18.2±2.3 (26.5) × (2.5) 3.8±1.1 (5) μm, n = 200, l/w (4-6.6), ellipsoid- fusoid, ends rounded, hyaline, smooth, septum median, slightly constricted at the septum, with hyaline, often elongate appendages at both ends, overlapping biseriate in the ascus. Each cell with 2 guttules.
Recommended publications
  • <I>Stilbosporaceae</I>
    Persoonia 33, 2014: 61–82 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158514X684212 Stilbosporaceae resurrected: generic reclassification and speciation H. Voglmayr1, W.M. Jaklitsch1 Key words Abstract Following the abolishment of dual nomenclature, Stilbospora is recognised as having priority over Prosthecium. The type species of Stilbospora, S. macrosperma, is the correct name for P. ellipsosporum, the type Alnecium species of Prosthecium. The closely related genus Stegonsporium is maintained as distinct from Stilbospora based Calospora on molecular phylogeny, morphology and host range. Stilbospora longicornuta and S. orientalis are described as Calosporella new species from Carpinus betulus and C. orientalis, respectively. They differ from the closely related Stilbospora ITS macrosperma, which also occurs on Carpinus, by longer, tapering gelatinous ascospore appendages and by dis- LSU tinct LSU, ITS rDNA, rpb2 and tef1 sequences. The asexual morphs of Stilbospora macrosperma, S. longicornuta molecular phylogeny and S. orientalis are morphologically indistinguishable; the connection to their sexual morphs is demonstrated by Phaeodiaporthe morphology and DNA sequences of single spore cultures derived from both ascospores and conidia. Both morphs rpb2 of the three Stilbospora species on Carpinus are described and illustrated. Other species previously recognised in systematics Prosthecium, specifically P. acerophilum, P. galeatum and P. opalus, are determined to belong to and are formally tef1 transferred to Stegonsporium. Isolates previously recognised as Stegonsporium pyriforme (syn. Prosthecium pyri­ forme) are determined to consist of three phylogenetically distinct lineages by rpb2 and tef1 sequence data, two of which are described as new species (S. protopyriforme, S. pseudopyriforme). Stegonsporium pyriforme is lectotypified and this species and Stilbospora macrosperma are epitypified.
    [Show full text]
  • A Novel Family of Diaporthales (Ascomycota)
    Phytotaxa 305 (3): 191–200 ISSN 1179-3155 (print edition) http://www.mapress.com/j/pt/ PHYTOTAXA Copyright © 2017 Magnolia Press Article ISSN 1179-3163 (online edition) https://doi.org/10.11646/phytotaxa.305.3.6 Melansporellaceae: a novel family of Diaporthales (Ascomycota) ZHUO DU1, KEVIN D. HYDE2, QIN YANG1, YING-MEI LIANG3 & CHENG-MING TIAN1* 1The Key Laboratory for Silviculture and Conservation of Ministry of Education, Beijing Forestry University, Beijing 100083, PR China 2International Fungal Research & Development Centre, The Research Institute of Resource Insects, Chinese Academy of Forestry, Bail- ongsi, Kunming 650224, PR China 3Museum of Beijing Forestry University, Beijing 100083, PR China *Correspondence author email: [email protected] Abstract Melansporellaceae fam. nov. is introduced to accommodate a genus of diaporthalean fungi that is a phytopathogen caus- ing walnut canker disease in China. The family is typified by Melansporella gen. nov. It can be distinguished from other diaporthalean families based on its irregularly uniseriate ascospores, and ovoid, brown conidia with a hyaline sheath and surface structures. Phylogenetic analysis shows that Melansporella juglandium sp. nov. forms a monophyletic group within Diaporthales (MP/ML/BI=100/96/1) and is a new diaporthalean clade, based on molecular data of ITS and LSU gene re- gions. Thus, a new family is proposed to accommodate this taxon. Key words: diaporthalean fungi, fungal diversity, new taxon, Sordariomycetes, systematics, taxonomy Introduction The ascomycetous order Diaporthales (Sordariomycetes) are well-known fungal plant pathogens, endophytes and saprobes, with wide distributions and broad host ranges (Castlebury et al. 2002, Rossman et al. 2007, Maharachchikumbura et al. 2016).
    [Show full text]
  • ©2015 Stephen J. Miller ALL RIGHTS RESERVED
    ©2015 Stephen J. Miller ALL RIGHTS RESERVED USE OF TRADITIONAL AND METAGENOMIC METHODS TO STUDY FUNGAL DIVERSITY IN DOGWOOD AND SWITCHGRASS. By STEPHEN J MILLER A dissertation submitted to the Graduate School-New Brunswick Rutgers, The State University of New Jersey In partial fulfillment of the requirements For the degree of Doctor of Philosophy Graduate Program in Plant Biology Written under the direction of Dr. Ning Zhang And approved by _____________________________________ _____________________________________ _____________________________________ _____________________________________ _____________________________________ New Brunswick, New Jersey October 2015 ABSTRACT OF THE DISSERTATION USE OF TRADITIONAL AND METAGENOMIC METHODS TO STUDY FUNGAL DIVERSITY IN DOGWOOD AND SWITCHGRASS BY STEPHEN J MILLER Dissertation Director: Dr. Ning Zhang Fungi are the second largest kingdom of eukaryotic life, composed of diverse and ecologically important organisms with pivotal roles and functions, such as decomposers, pathogens, and mutualistic symbionts. Fungal endophyte studies have increased rapidly over the past decade, using traditional culturing or by utilizing Next Generation Sequencing (NGS) to recover fastidious or rare taxa. Despite increasing interest in fungal endophytes, there is still an enormous amount of ecological diversity that remains poorly understood. In this dissertation, I explore the fungal endophyte biodiversity associated within two plant hosts (Cornus L. species) and (Panicum virgatum L.), create a NGS pipeline, facilitating comparison between traditional culturing method and culture- independent metagenomic method. The diversity and functions of fungal endophytes inhabiting leaves of woody plants in the temperate region are not well understood. I explored the fungal biodiversity in native Cornus species of North American and Japan using traditional culturing ii techniques. Samples were collected from regions with similar climate and comparison of fungi was done using two years of collection data.
    [Show full text]
  • Leaf-Inhabiting Genera of the Gnomoniaceae, Diaporthales
    Studies in Mycology 62 (2008) Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales M.V. Sogonov, L.A. Castlebury, A.Y. Rossman, L.C. Mejía and J.F. White CBS Fungal Biodiversity Centre, Utrecht, The Netherlands An institute of the Royal Netherlands Academy of Arts and Sciences Leaf-inhabiting genera of the Gnomoniaceae, Diaporthales STUDIE S IN MYCOLOGY 62, 2008 Studies in Mycology The Studies in Mycology is an international journal which publishes systematic monographs of filamentous fungi and yeasts, and in rare occasions the proceedings of special meetings related to all fields of mycology, biotechnology, ecology, molecular biology, pathology and systematics. For instructions for authors see www.cbs.knaw.nl. EXECUTIVE EDITOR Prof. dr Robert A. Samson, CBS Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands. E-mail: [email protected] LAYOUT EDITOR Marianne de Boeij, CBS Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands. E-mail: [email protected] SCIENTIFIC EDITOR S Prof. dr Uwe Braun, Martin-Luther-Universität, Institut für Geobotanik und Botanischer Garten, Herbarium, Neuwerk 21, D-06099 Halle, Germany. E-mail: [email protected] Prof. dr Pedro W. Crous, CBS Fungal Biodiversity Centre, P.O. Box 85167, 3508 AD Utrecht, The Netherlands. E-mail: [email protected] Prof. dr David M. Geiser, Department of Plant Pathology, 121 Buckhout Laboratory, Pennsylvania State University, University Park, PA, U.S.A. 16802. E-mail: [email protected] Dr Lorelei L. Norvell, Pacific Northwest Mycology Service, 6720 NW Skyline Blvd, Portland, OR, U.S.A.
    [Show full text]
  • <I>Acrocordiella</I>
    Persoonia 37, 2016: 82–105 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158516X690475 Resolution of morphology-based taxonomic delusions: Acrocordiella, Basiseptospora, Blogiascospora, Clypeosphaeria, Hymenopleella, Lepteutypa, Pseudapiospora, Requienella, Seiridium and Strickeria W.M. Jaklitsch1,2, A. Gardiennet3, H. Voglmayr2 Key words Abstract Fresh material, type studies and molecular phylogeny were used to clarify phylogenetic relationships of the nine genera Acrocordiella, Blogiascospora, Clypeosphaeria, Hymenopleella, Lepteutypa, Pseudapiospora, Ascomycota Requienella, Seiridium and Strickeria. At first sight, some of these genera do not seem to have much in com- Dothideomycetes mon, but all were found to belong to the Xylariales, based on their generic types. Thus, the most peculiar finding new genus is the phylogenetic affinity of the genera Acrocordiella, Requienella and Strickeria, which had been classified in phylogenetic analysis the Dothideomycetes or Eurotiomycetes, to the Xylariales. Acrocordiella and Requienella are closely related but pyrenomycetes distinct genera of the Requienellaceae. Although their ascospores are similar to those of Lepteutypa, phylogenetic Pyrenulales analyses do not reveal a particularly close relationship. The generic type of Lepteutypa, L. fuckelii, belongs to the Sordariomycetes Amphisphaeriaceae. Lepteutypa sambuci is newly described. Hymenopleella is recognised as phylogenetically Xylariales distinct from Lepteutypa, and Hymenopleella hippophaëicola is proposed as new name for its generic type, Spha­ eria (= Lepteutypa) hippophaës. Clypeosphaeria uniseptata is combined in Lepteutypa. No asexual morphs have been detected in species of Lepteutypa. Pseudomassaria fallax, unrelated to the generic type, P. chondrospora, is transferred to the new genus Basiseptospora, the genus Pseudapiospora is revived for P. corni, and Pseudomas­ saria carolinensis is combined in Beltraniella (Beltraniaceae).
    [Show full text]
  • Myconet Volume 14 Part One. Outine of Ascomycota – 2009 Part Two
    (topsheet) Myconet Volume 14 Part One. Outine of Ascomycota – 2009 Part Two. Notes on ascomycete systematics. Nos. 4751 – 5113. Fieldiana, Botany H. Thorsten Lumbsch Dept. of Botany Field Museum 1400 S. Lake Shore Dr. Chicago, IL 60605 (312) 665-7881 fax: 312-665-7158 e-mail: [email protected] Sabine M. Huhndorf Dept. of Botany Field Museum 1400 S. Lake Shore Dr. Chicago, IL 60605 (312) 665-7855 fax: 312-665-7158 e-mail: [email protected] 1 (cover page) FIELDIANA Botany NEW SERIES NO 00 Myconet Volume 14 Part One. Outine of Ascomycota – 2009 Part Two. Notes on ascomycete systematics. Nos. 4751 – 5113 H. Thorsten Lumbsch Sabine M. Huhndorf [Date] Publication 0000 PUBLISHED BY THE FIELD MUSEUM OF NATURAL HISTORY 2 Table of Contents Abstract Part One. Outline of Ascomycota - 2009 Introduction Literature Cited Index to Ascomycota Subphylum Taphrinomycotina Class Neolectomycetes Class Pneumocystidomycetes Class Schizosaccharomycetes Class Taphrinomycetes Subphylum Saccharomycotina Class Saccharomycetes Subphylum Pezizomycotina Class Arthoniomycetes Class Dothideomycetes Subclass Dothideomycetidae Subclass Pleosporomycetidae Dothideomycetes incertae sedis: orders, families, genera Class Eurotiomycetes Subclass Chaetothyriomycetidae Subclass Eurotiomycetidae Subclass Mycocaliciomycetidae Class Geoglossomycetes Class Laboulbeniomycetes Class Lecanoromycetes Subclass Acarosporomycetidae Subclass Lecanoromycetidae Subclass Ostropomycetidae 3 Lecanoromycetes incertae sedis: orders, genera Class Leotiomycetes Leotiomycetes incertae sedis: families, genera Class Lichinomycetes Class Orbiliomycetes Class Pezizomycetes Class Sordariomycetes Subclass Hypocreomycetidae Subclass Sordariomycetidae Subclass Xylariomycetidae Sordariomycetes incertae sedis: orders, families, genera Pezizomycotina incertae sedis: orders, families Part Two. Notes on ascomycete systematics. Nos. 4751 – 5113 Introduction Literature Cited 4 Abstract Part One presents the current classification that includes all accepted genera and higher taxa above the generic level in the phylum Ascomycota.
    [Show full text]
  • Diaporthales)
    Persoonia 38, 2017: 136–155 ISSN (Online) 1878-9080 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE https://doi.org/10.3767/003158517X694768 Juglanconis gen. nov. on Juglandaceae, and the new family Juglanconidaceae (Diaporthales) H. Voglmayr1, L.A. Castlebury2, W.M. Jaklitsch1,3 Key words Abstract Molecular phylogenetic analyses of ITS-LSU rDNA sequence data demonstrate that Melanconis species occurring on Juglandaceae are phylogenetically distinct from Melanconis s.str., and therefore the new genus Juglan- Ascomycota conis is described. Morphologically, the genus Juglanconis differs from Melanconis by light to dark brown conidia with Diaporthales irregular verrucae on the inner surface of the conidial wall, while in Melanconis s.str. they are smooth. Juglanconis molecular phylogeny forms a separate clade not affiliated with a described family of Diaporthales, and the family Juglanconidaceae is new species introduced to accommodate it. Data of macro- and microscopic morphology and phylogenetic multilocus analyses pathogen of partial nuSSU-ITS-LSU rDNA, cal, his, ms204, rpb1, rpb2, tef1 and tub2 sequences revealed four distinct species systematics of Juglanconis. Comparison of the markers revealed that tef1 introns are the best performing markers for species delimitation, followed by cal, ms204 and tub2. The ITS, which is the primary barcoding locus for fungi, is amongst the poorest performing markers analysed, due to the comparatively low number of informative characters. Melanconium juglandinum (= Melanconis carthusiana), M. oblongum (= Melanconis juglandis) and M. pterocaryae are formally combined into Juglanconis, and J. appendiculata is described as a new species. Melanconium juglandinum and Melanconis carthusiana are neotypified and M. oblongum and Diaporthe juglandis are lectotypified. A short descrip- tion and illustrations of the holotype of Melanconium ershadii from Pterocarya fraxinifolia are given, but based on morphology it is not considered to belong to Juglanconis.
    [Show full text]
  • A Checklist of Norwegian Sordariomycetes
    A checklist of Norwegian Sordariomycetes Björn Nordén1, John Bjarne Jordal2 1Norwegian Institute for Nature Research (NINA), Gaustadalleen 21, NO-0349 Oslo, Norway 2Auragata 3, 6600 Sunndalsøra, Norway Corresponding author: [email protected] mentioned that ‘To decide what the correct epithet and author citation for a species should Norsk tittel: En sjekkliste over kjernesopper i be, is the work of a specialist’. The present Norge list attempts to provide updated information on new finds and nomenclature. Specific data Nordén B, Jordal JB, 2015. A checklist of on the ecology and distribution of the species Norwegian Sordariomycetes. Agarica 2015 in Norway can be gathered from the cited vol. 36: 55-73. data sources, while more general data on for example substrate relations can be found in KEYWORDS Eriksson (2014) and at http://www8.umu.se/ Ascomycetes, wood-living fungi, wood- myconet/asco/vasc/index.html. decaying fungi, corticolous fungi, pyreno- mycetes, temperate deciduous forest MATERIALS AND METHODS The list is based on data from Aarnæs (2002), NØKKELORD Norsk Soppdatabase (NSD, 2015), the Sekksporesopp, vedboende sopp, barkboende Norwegian Biodiversity Information Centre sopp, pyrenomyceter, edelløvskog (“Artsdatabanken” & GBIF Norway (2015), also called “Artskart”), other relevant SAMMENDRAG literature, and the study of own material and Sjekklista omfatter alle kjernesopper (pyreno- material from public herbaria in Norway. In myceter) tilhørende klassen Sordariomycetes the list, NSD (2015) is not cited separately, som er kjent fra Norge og inkluderer 590 arter. since it was merged with Artskart. However, Lista er basert på gjennomgang av herbarie- NSD should be consulted if information is not materiale, litteratur og egne undersøkelser found in Artskart since some of the infor- 2011-2015.
    [Show full text]
  • Generic Reclassification and Speciation
    Persoonia 33, 2014: 61–82 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158514X684212 Stilbosporaceae resurrected: generic reclassification and speciation H. Voglmayr1, W.M. Jaklitsch1 Key words Abstract Following the abolishment of dual nomenclature, Stilbospora is recognised as having priority over Prosthecium. The type species of Stilbospora, S. macrosperma, is the correct name for P. ellipsosporum, the type Alnecium species of Prosthecium. The closely related genus Stegonsporium is maintained as distinct from Stilbospora based Calospora on molecular phylogeny, morphology and host range. Stilbospora longicornuta and S. orientalis are described as Calosporella new species from Carpinus betulus and C. orientalis, respectively. They differ from the closely related Stilbospora ITS macrosperma, which also occurs on Carpinus, by longer, tapering gelatinous ascospore appendages and by dis- LSU tinct LSU, ITS rDNA, rpb2 and tef1 sequences. The asexual morphs of Stilbospora macrosperma, S. longicornuta molecular phylogeny and S. orientalis are morphologically indistinguishable; the connection to their sexual morphs is demonstrated by Phaeodiaporthe morphology and DNA sequences of single spore cultures derived from both ascospores and conidia. Both morphs rpb2 of the three Stilbospora species on Carpinus are described and illustrated. Other species previously recognised in systematics Prosthecium, specifically P. acerophilum, P. galeatum and P. opalus, are determined to belong to and are formally tef1 transferred to Stegonsporium. Isolates previously recognised as Stegonsporium pyriforme (syn. Prosthecium pyri­ forme) are determined to consist of three phylogenetically distinct lineages by rpb2 and tef1 sequence data, two of which are described as new species (S. protopyriforme, S. pseudopyriforme). Stegonsporium pyriforme is lectotypified and this species and Stilbospora macrosperma are epitypified.
    [Show full text]
  • Xylariales, Ascomycota), Designation of an Epitype for the Type Species of Iodosphaeria, I
    VOLUME 8 DECEMBER 2021 Fungal Systematics and Evolution PAGES 49–64 doi.org/10.3114/fuse.2021.08.05 Phylogenetic placement of Iodosphaeriaceae (Xylariales, Ascomycota), designation of an epitype for the type species of Iodosphaeria, I. phyllophila, and description of I. foliicola sp. nov. A.N. Miller1*, M. Réblová2 1Illinois Natural History Survey, University of Illinois Urbana-Champaign, Champaign, IL, USA 2Czech Academy of Sciences, Institute of Botany, 252 43 Průhonice, Czech Republic *Corresponding author: [email protected] Key words: Abstract: The Iodosphaeriaceae is represented by the single genus, Iodosphaeria, which is composed of nine species with 1 new taxon superficial, black, globose ascomata covered with long, flexuous, brown hairs projecting from the ascomata in a stellate epitypification fashion, unitunicate asci with an amyloid apical ring or ring lacking and ellipsoidal, ellipsoidal-fusiform or allantoid, hyaline, phylogeny aseptate ascospores. Members of Iodosphaeria are infrequently found worldwide as saprobes on various hosts and a wide systematics range of substrates. Only three species have been sequenced and included in phylogenetic analyses, but the type species, taxonomy I. phyllophila, lacks sequence data. In order to stabilize the placement of the genus and family, an epitype for the type species was designated after obtaining ITS sequence data and conducting maximum likelihood and Bayesian phylogenetic analyses. Iodosphaeria foliicola occurring on overwintered Alnus sp. leaves is described as new. Five species in the genus form a well-supported monophyletic group, sister to thePseudosporidesmiaceae in the Xylariales. Selenosporella-like and/or ceratosporium-like synasexual morphs were experimentally verified or found associated with ascomata of seven of the nine accepted species in the genus.
    [Show full text]
  • Anthracnose Disease of Walnut- a Review Mudasir Hassan, Khurshid Ahmad
    International Journal of Environment, Agriculture and Biotechnology (IJEAB) Vol-2, Issue -5, Sep-Oct- 2017 http://dx.doi.org/10.22161/ijeab/2.5.6 ISSN: 2456-1878 Anthracnose Disease of Walnut- A Review Mudasir Hassan, Khurshid Ahmad Department of Plant Pathology, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir, Shalimar Campus, 191 121, Jammu & Kashmir, India Abstract— Walnut (Juglans regia) an important originated in Iran from where it was distributed throughout commercial dry fruit crop, is attacked by several diseases the world (Arora, 1985). It is mainly grown in china, USA causing economic damage and amongst them walnut and Iran, whereas India stands seventh in production anthracnose caused by Marssonina juglandis (Lib.) Magnus accounting upto 2.14 per cent of the world walnut has posed a serious threat to this crop in India and abroad. production (Anonymous, 2010). In India, walnut is grown Walnut anthracnose results in reduction in quantitative in Jammu and Kashmir, Arunachal Pradesh, Himachal parameters such as size, mass and actual crop of nuts, Pradesh and Uttarakhand. In J&K, Walnut is grown in failure in metabolic processes in leaves and change in Badrawah, Poonch, Kupwara, Baramulla, Bandipora, biochemical indices. Premature loss of leaves results in Ganderbal, Budgam, Srinagar, Anantnag and other hilly poorly-filled, low-quality, and darkened kernels. The areas occupying an area of 83,219 ha with an annual disease initially appears on leaves as brown to black production of 20,873 tonnes (Anonymous, 2012). Jammu coloured circular to irregularly circular spots. These spots and Kashmir State has attained a special place in the eventually enlarge and coalesce into large necrotic areas.
    [Show full text]
  • A Review of the Phylogeny and Biology of the Diaporthales
    Mycoscience (2007) 48:135–144 © The Mycological Society of Japan and Springer 2007 DOI 10.1007/s10267-007-0347-7 REVIEW Amy Y. Rossman · David F. Farr · Lisa A. Castlebury A review of the phylogeny and biology of the Diaporthales Received: November 21, 2006 / Accepted: February 11, 2007 Abstract The ascomycete order Diaporthales is reviewed dieback [Apiognomonia quercina (Kleb.) Höhn.], cherry based on recent phylogenetic data that outline the families leaf scorch [A. erythrostoma (Pers.) Höhn.], sycamore can- and integrate related asexual fungi. The order now consists ker [A. veneta (Sacc. & Speg.) Höhn.], and ash anthracnose of nine families, one of which is newly recognized as [Gnomoniella fraxinii Redlin & Stack, anamorph Discula Schizoparmeaceae fam. nov., and two families are recircum- fraxinea (Peck) Redlin & Stack] in the Gnomoniaceae. scribed. Schizoparmeaceae fam. nov., based on the genus Diseases caused by anamorphic members of the Diaportha- Schizoparme with its anamorphic state Pilidella and includ- les include dogwood anthracnose (Discula destructiva ing the related Coniella, is distinguished by the three- Redlin) and butternut canker (Sirococcus clavigignenti- layered ascomatal wall and the basal pad from which the juglandacearum Nair et al.), both solely asexually reproduc- conidiogenous cells originate. Pseudovalsaceae is recog- ing species in the Gnomoniaceae. Species of Cytospora, the nized in a restricted sense, and Sydowiellaceae is circum- anamorphic state of Valsa, in the Valsaceae cause diseases scribed more broadly than originally conceived. Many on Eucalyptus (Adams et al. 2005), as do species of Chryso- species in the Diaporthales are saprobes, although some are porthe and its anamorphic state Chrysoporthella (Gryzen- pathogenic on woody plants such as Cryphonectria parasit- hout et al.
    [Show full text]