19. Herpotrichia macrotricha (SMH269) A–B. Ascomata.
 C. Ascomatal section. D. Ascus. E. Ascospore. 20. H.
 macrotricha (GKM196N) A. Ascoma. B. Ascomatal section. C. Ascus. D.
 Ascospores. 21. H. macrotricha (GKM1128) A–B. Ascomata.
 C. Ascus. D. Ascospores. 22. H. macrotricha (SMH4913)
 A–B. Ascomata. C. Ascomatal neck section. D. Ascomatal wall section. E.
 Ascomatal section. F. Ascus. G, H. Ascospores. 23. H. cf.
 herpotrichoides (GKM212N) A–B. Ascomata. C. Ascus. D.
 Ascospores. 24. H. cf. herpotrichoides (SMH5167)
 A–B. Ascomata. C. Ascus. D. Ascospores. Scale bars: Ascomata = 500
 μm. Section = 100 μm. Wall = 10 μm. Ascus = 10 μm. Ascospore = 10
 μm.

19. Herpotrichia macrotricha (SMH269) A–B. Ascomata. C. Ascomatal section. D. Ascus. E. Ascospore. 20. H. macrotricha (GKM196N) A. Ascoma. B. Ascomatal section. C. Ascus. D. Ascospores. 21. H. macrotricha (GKM1128) A–B. Ascomata. C. Ascus. D. Ascospores. 22. H. macrotricha (SMH4913) A–B. Ascomata. C. Ascomatal neck section. D. Ascomatal wall section. E. Ascomatal section. F. Ascus. G, H. Ascospores. 23. H. cf. herpotrichoides (GKM212N) A–B. Ascomata. C. Ascus. D. Ascospores. 24. H. cf. herpotrichoides (SMH5167) A–B. Ascomata. C. Ascus. D. Ascospores. Scale bars: Ascomata = 500 μm. Section = 100 μm. Wall = 10 μm. Ascus = 10 μm. Ascospore = 10 μm.

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... Notes. Magnibotryascoma was proposed to accommodate M. uniseriatum which was transferred from Misturatosphaeria uniseriatum based on its unique morphology (Mugambi and Huhndorf 2009;Thambugala et al. 2015). For taxonomic treatment of this genus, we follow Hongsanan et al. (2020), Tennakoon et al. (2021) and Wijayawardene et al. (2022). ...
... Byssosphaeria is a monophyletic genus in Melanommataceae based on morphology and multi-gene phylogenetic analysis (Hyde et al. , 2013Mugambi and Huhndorf 2009;Zhang et al. 2012). Our new species B. guangdongense formed an independent clade in the phylogenetic tree ( Figure 1) with strong statistical support. ...
... & M.A. Curtis) Höhn. has been recovered in 2009 as strongly supported monophyletic group outside the Pleosporales [ 3 ]. More recently [ 4,5 ] accepted family Tubeufiaceae in the Tubeufiales (Dothideomycetes), a fact predicted by [ 6 ]. ...
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... Subsequently, researchers started using protein-coding genes (e.g., TEF1, BenA, CaM, TUB, etc.) for fungal identification under the phylogenetic species concepts. However, standardization was lacking [73][74][75], and no cutoff scores for fungal species identification were available [76]. Furthermore, ANI analysis is not regularly used for the identification of fungi as practiced for bacterial species because fungal genomes are complex and their WGS are scarce in public databases [77]. ...
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... Aurantiascoma Thambug. & K.D. Hyde Thambugala et al. (2015) introduced Aurantiascoma to accommodate A. minimum as the type species, which was previously known as Misturatosphaeria minima (Mugambi andHuhndorf 2009). Jaklitsch et al. (2016) synonymized Aurantiascoma under Teichospora and erected Misturatosphaeria minima as T. parva. ...
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... As a result of this work, Barr (1990) confi rmed that P. mutabilis should be the correct name for the species, while the other names mentioned above were indicated as synonyms. Currently, the name P. mutabilis is generally recognized and widely used in recent publications (Mugambi & Huhndorf, 2009;Checa et al., 2013;Jaklitsch & Voglmayr, 2017;Index Fungorum, 2022). ...
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... f r a x i n i n a , b u t o n l y Pleosporomycetidae subclass of Dothideomycetes. Hongsanan et al. (2020), analyzing the results of studies by other authors, found that phylogenetically, Herpotrichia is polyphyletic (Mugambi and Huhndorf 2009;Zhang et al. 2012;Tian et al. 2015;Hashimoto et al. 2017;Wanasinghe et al. 2018). Unfortunately, only a few works include H. parasitica in their phylogenetic analyzes (Crous et al. 2015;Tian et al. 2015). ...
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... et P. Syd., Phyllostictaceae, Botryosphaeriales, and Phoma Sacc., Didymellaceae, Pleosporales) and teleomorphic (e.g., species of the genera Leptosphaeria Ces. et De Not., Leptosphaeriaceae, Pleosporales, Herpotrichia Fuckel, Melanommataceae, Pleosporales, Dothiora Fr., Dothideaceae, Dothideales, and Mycosphaerella Johanson, Mycosphaerellaceae, Capnodiales) (e.g., Suzuki, 1910;Barr, 1984Barr, , 2001Funk, 1985;Ganley et al., 2004;Crous et al., 2007a;Mugambi and Huhndorf, 2009;Aveskamp et al., 2010;Strobel et al., 2011;Zhang et al., 2011;Phillips et al., 2013;Taylor et al., 2015;Slippers et al., 2017;Busskamp et al, 2020). ...
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The types of damage to Cupressaceae and Pinaceae conifers from the Arkhara-Boguchan, Belaya Gora, and Progress localities (Amur Region, Russia; Paleocene) are analyzed. Most of the damage types were caused by various microscopic fungi of the Ascomycota. Fungal remains are represented by hyphae, chains of conidia, different fruiting bodies, and dispersed spores of three types. The problem of differentiation of morphologically similar damage caused by arthropods and micromycetes is discussed. The abundance of diverse micromycetes on various organs of Paleocene conifers is consistent with previously obtained data on the existence of these plants in a temperate humid climate with a hot summer and without a dry season.