Published July 10, 2024
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Taxonomic treatment
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Drepanopezizaceae Baral
Creators
- 1. Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China & Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand
- 2. Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand
- 3. School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand
- 4. Key Laboratory of Phytochemistry and Natural Medicines, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, China
Description
Drepanopezizaceae Baral
Fig. 3
Type.
Drepanopeziza (Kleb.) Jaap 1914.
Description.
Sexual morph: Ascomata small-sized, up to 2 mm in diameter, apothecial, cupulate, margin often protruding, with or without lobes, sessile and mostly immersed. Excipulum is composed of cells of textura angularis. Paraphyses hyaline, thin-walled, aseptate or septate, apically swollen. Asci 4–8 - spored, clavate or cylindrical, apex obtuse to conical, with or without apical ring. Ascospores ellipsoid to fusoid, aseptate or 1–2 - septate. Asexual morph: Conidiomata solitary to gregarious or confluent, mostly epiphyllous, acervulus. Conidiogenesis holoblastic. Conidia hyaline, thin-walled.
Notes.
Drepanopezizaceae was described with sexual and asexual morphs. Both life morphs were found as parasitic on leaves of various dicotyledons, and rarely on herbaceous (Johnston et al. 2019). The sexual morph is recognized by the cupulate, apothecial ascomata, and the paraphyses with swollen apical (Harada et al. 1974; Williamson and Bernard 1988; Spiers and Hopcroft 1998). The asexual morph is acervular but varies in conidial shape among genera (Crous et al. 2009; Khodadadi et al. 2022). The family name was first time used by Batista and Maia (1960), but was invalid because of unavailable diagnosis or description (Johnston et al. 2019). It was difficult to trace back the history of members accommodated in the family until Johnston et al. (2019), validated the family name based on the phylogenetic analysis (Table 2).
The taxa used in the phylogenetic analysis are labeled in bold.
Notes
Published as part of Yang, Hong De, Jayawardena, Ruvishika S., Zeng, Xiang Yu, Thiyagaraja, Vinodhini, Zhao, Qi & Hyde, Kevin D., 2024, Recommendations on approving the name " Entomosporium ", with a new species, E. dichotomanthes from China (Leotiomycetes, Drepanopezizaceae), pp. 1-20 in MycoKeys 107 on pages 1-20, DOI: 10.3897/mycokeys.107.121962
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Linked records
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Additional details
Identifiers
Biodiversity
- Family
- Drepanopezizaceae
- Kingdom
- Fungi
- Order
- Helotiales
- Phylum
- Ascomycota
- Scientific name authorship
- Baral
- Taxon rank
- family
References
- Wolf F (1912) The perfect stage of Actinonema rosae. Botanical Gazette (Chicago, Ill.) 54 (3): 218–234. https://doi.org/10.1086/330900
- Lee HT, Shin HD (2000) Taxonomic Studies on the Genus Marssonina in Korea. Mycobiology 28 (1): 39–46. https://doi.org/10.1080/12298093.2000.12015720
- Stowell EA, Backus MP (1967) Morphology and cytology of Diplocarpon maculatum on Crataegus. II. Initiation and development of the apothecium. Mycologia 59 (4): 623–636. https://doi.org/10.1080/00275514.1967.12018456
- Chen H, White JF, Malik K, Qi F, Li C (2022) Diplocarpon mespilicola sp. nov. associated with Entomosporium leaf spot on hawthorn in China. Plant Disease 106 (11): 2884–2891. https://doi.org/10.1094/PDIS-01-22-0097-RE
- Spiers AG, Hopcroft DH (1998) Morphology of Drepanopeziza species pathogenic to poplars. Mycological Research 102 (9): 1025–1037. https://doi.org/10.1017/S0953756297005972
- Williamson MA, Bernard EC (1988) Life cycle of a new species of Blumeriella (Ascomycotina: Dermateaceae), a leaf-spot pathogen of spirea. Canadian Journal of Botany 66 (10): 2048–2054. https://doi.org/10.1139/b88-280
- Crous PW, Braun U, Wingfield MJ, Wood AR, Shin HD, Summerell BA, Alfenas AC, Cumagun CJR, Groenewald JZ (2009) Phylogeny and taxonomy of obscure genera of microfungi. Persoonia. Persoonia 22 (1): 139–161. https://doi.org/10.3767/003158509X461701
- Wiese MV, Ravenscroft AV (1978) Sporodochium development and conidium production in Cephalosporium gramineum. Phytopathology 68 (3): 395. https://doi.org/10.1094/Phyto-68-395
- Kirchner OV, Boltshauser H (1987) Atlas der Krankheiten unserer landwirtschaftlichen Kulturpflanzen 3. Serie: Wurzelgewächse und Handelsgewächse (2. Auflage). Verlag Von Eugen Ulmer, 127 pp.
- Johnston PR, Quijada L, Smith CA, Baral HO, Hosoya T, Baschien C, Pärtel K, Zhuang WY, Haelewaters D, Park D, Carl S, López-Giráldez F, Wang Z, Townsend JP (2019) A multigene phylogeny toward a new phylogenetic classification of Leotiomycetes. IMA Fungus 10 (1): 1–22. https://doi.org/10.1186/s43008-019-0002-x
- Harada Y, Sawamura K, Konno K (1974) Diplocarpon mali, sp. nov., the perfect state of apple blotch fungus Marssonina coronaria. Japanese Journal of Phytopathology 40 (5): 412–418. https://doi.org/10.3186/jjphytopath.40.412
- Khodadadi F, Martin PL, Donahue DJ, Peter KA, Acimovic SAG (2022) Characterizations of an emerging disease: Apple blotch caused by Diplocarpon coronariae (syn. Marssonina coronaria) in the mid-atlantic United States. Plant Disease 106 (7): 1803–1817. https://doi.org/10.1094/PDIS-11-21-2557-RE
- Batista AC, Maia HS (1960) Discomycetes alienigenas (1). Saccardoa 1: 98–102.
- Wijayawardene NN, Hyde KD, Rajeshkumar KC, Hawksworth DL, Madrid H, Kirk PM, Braun U, Singh RV, Crous PW, Kukwa M, Lücking R, Kurtzman CP, Yurkov A, Haelewaters D, Aptroot A, Thorsten Lumbsch H, Timdal E, Ertz D, Etayo J, Phillips AJL, Groenewald JZ, Papizadeh M, Selbmann L, Dayarathne MC, Weerakoon G, Gareth Jones EB, Suetrong S, Tian Q, Castañeda-Ruiz RF, Bahkali AH, Pang KL, Tanaka K, Dai DQ, Sakayaroj J, Hujslová M, Lombard L, Shenoy BD, Suija A, Maharachchikumbura SSN, Thambugala KM, Wanasinghe DN, Sharma BO, Gaikwad S, Pandit G, Zucconi L, Onofri S, Egidi E, Raja HA, Kodsueb R, Cáceres MES, Pérez-Ortega S, Fiuza PO, Monteiro JS, Vasilyeva LN, Shivas RG, Prieto M, Wedin M, Olariaga I, Lateef AA, Agrawal Y, Fazeli SAS, Amoozegar MA, Zhao GZ, Pfliegler WP, Sharma G, Oset M, Abdel-Wahab MA, Takamatsu S, Bensch K, De Silva NI, De Kesel A, Karunarathna A, Boonmee S, Pfister DH, Lu YZ, Luo ZL, Boonyuen N, Daranagama DA, Senanayake IC, Jayasiri SC, Samarakoon MC, Zeng XY, Doilom M, Quijada L, Rampadarath S, Heredia G, Dissanayake AJ, Jayawardana RS, Perera RH, Tang LZ, Phukhamsakda C, Hernández-Restrepo M, Ma X, Tibpromma S, Gusmao LFP, Weerahewa D, Karunarathna SC (2017) Notes for genera: Ascomycota. Fungal Diversity 86 (1): 1–594. https://doi.org/10.1007/s13225-017-0386-0
- Ekanayaka AH, Hyde KD, Gentekaki E, McKenzie EHC, Zhao Q, Bulgakov TS, Camporesi E (2019) Preliminary classification of Leotiomycetes. Mycosphere 10 (1): 310–489. https://doi.org/10.5943/mycosphere/10/1/7
- Wijayawardene NN, Hyde KD, Dai DQ, Sánchez-García M, Goto BT, Saxena RK, Erdoğdu M, Selçuk F, Rajeshkumar KC, Aptroot A, Błaszkowski J, Boonyuen N, da Silva GA, de Souza FA, Dong W, Ertz D, Haelewaters D, Jones EBG, Karunarathna SC, Kirk PM, Kukwa M, Kumla J, Leontyev DV, Lumbsch HT, Maharachchikumbura SSN, Marguno F, Martínez-Rodríguez P, Mešić A, Monteiro JS, Oehl F, Pawłowska J, Pem D, Pfliegler WP, Phillips AJL, Pošta A, He MQ, Li JX, Raza M, Sruthi OP, Suetrong S, Suwannarach N, Tedersoo L, Thiyagaraja V, Tibpromma S, Tkalčec Z, Tokarev YS, Wanasinghe DN, Wijesundara DSA, Wimalaseana SDMK, Madrid H, Zhang GQ, Gao Y, Sánchez-Castro I, Tang LZ, Stadler M, Yurkov A, Thines M (2022) Outline of Fungi and fungus-like taxa – 2021. Mycosphere 13 (1): 53–453. https://doi.org/10.5943/mycosphere/13/1/2
- Zhu ZX, Dugan F, Murray TD (2023) A multilocus phylogeny places Hymenula cerealis (syn. Cephalosporium gramineum) in the Helotiales, Leotiomycetes. Phytopathology 113 (7): 1254–1265. https://doi.org/10.1094/PHYTO-05-22-0151-R