– Seimatosporium rosae ( epitype ) . a Habit in wood. b, c Fruiting bodies on host substrate. d Cross section of fruiting body. e, f Peridium. g, h, i Conidiogenous cells. j, k, l Mature conidia. m Germinating spore on PDA. n from above. o from below. Bars: c = 200 μm ; d = 300 μm ; e, g, h, i, m = 20 μm ; f= 50 μm ; j, k, l = 10 μm . 

– Seimatosporium rosae ( epitype ) . a Habit in wood. b, c Fruiting bodies on host substrate. d Cross section of fruiting body. e, f Peridium. g, h, i Conidiogenous cells. j, k, l Mature conidia. m Germinating spore on PDA. n from above. o from below. Bars: c = 200 μm ; d = 300 μm ; e, g, h, i, m = 20 μm ; f= 50 μm ; j, k, l = 10 μm . 

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The genus Seimatosporium is saprobic or pathogenic on plants, and are 'pestalotioid fungi'. The genus presently belongs in Discosiaceae (Amphisphaeriales) and includes 78 species epithets. In this study, we observed three specimens of Seimatosporium from Russia and they are characterized by morphological and sequence data. We analyzed combined ITS...

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... salicinum and Seim. rosae (Nag Raj 1993, Kobayashi 2007, Mułenko et al. 2008, Norphanphoun et al. 2015. Seimatosporium centrale has larger conidia than Seim. ...
... parvum is separated from Seim. rosae which has also been reported from Rosa based on phylogenetic analysis (Norphanphoun et al. 2015) (Fig. 6). Furthermore, Seim. ...
... Moreover, the conidia of Spo. lichenicola are 4 -5-septate, which is also an important morphological characteristic distinguishing it from other species in Sporocadus (Norphanphoun et al. 2015 (Fig. 8), but the conidia of Spo. rosarum have an apical appendage, which makes it easy to distinguish them from other species of Sporocadus (Wanasinghe et al. 2018. ...
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... Several fungi within the family of Sporocadaceae (Xylariales, Sordariomycetes) have been reported as saprophytes, endophytes, and plant pathogens in a wide host range [14][15][16][17][18][19]. More specifically, species within Neopestalotiopsis Maharachch., K.D. Hyde and Crous, ...
... Seimatosporium and Sporocadus consist predominately of endophytes and saprobes of woody plants [17,33,34,43], although some species are pathogens of different plant hosts, such as eucalypt, blackberry, and grapevine [13,54,55]. More specifically, out of the nine Seimatosporium species previously reported from diseased or dead grapevine wood worldwide, only five (Seim. ...
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... The fungus had the following morphology: Lesions beginning as numerous, small irregular or angular blackened areas on leaves 1 6 mm wide later surrounded by reddish brown poorly defined necrotic areas developing a greyish center, coalescing and leading to entire necrosis of leaves and defoliation of plants; Conidiomata acervular, sub-epidermal, 26-106 μm diam., dark brown; Conidiogenous cells cylindrical, holoblastic, phialidic, 4-12 × 2-3 μm, hyaline, smooth; Conidia fusiform, straight or curved, 12-24 × 3-5 μm, 3 − septate, two median cells, medium brown, apical cells hyaline, each terminal cell bearing two unbranched, whip-like, hyaline appendages, 8-23 μm long ( Fig. 1c-e). This morphology is equivalent to that of Seimatosporium hypericinum, as described in Sutton (1980) andNag Raj (1993). ...
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... ericacearum: 13-15 × 4.4-6.5 μm. Norphanphoun et al. [16] designated a reference specimen of Seim. lichenicola from Cotinus coggygria with conidial dimensions similar to Syn. ericacearum and Seim. ...
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... Genus Seimatosporium was erected with S. rosae Corda as the type species and consists predominately of saprobes and endophytes of woody plants Norphanphoun et al. 2015;Perera et al. 2016;Wijayawardene et al. 2016), although some species are pathogens (e.g., Leaf spot of eucalypts) (Barber et al. 2011). The genus is characterized by producing holoblastic or annelidic conidiogenous cells within acervuli or pycnidia that produce multiseptate conidia with pigmented median cells, a truncate basal cell with or without an eccentrically positioned appendage, and with or without a centrally positioned unbranched apical appendage (Nag Raj 1993). ...
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... (Sutton 1980). The genus Melanconis belongs in the family Melanconidaceae in Diaporthales, Sordariomycetes (Maharachchikumbura et al. 2015(Maharachchikumbura et al. , 2016. Castlebury et al. (2002) used LSU sequence data from M. stilbostoma (Fr.) ...
... Thus, Castlebury et al. (2002) placed Melanconis desmazieri and Hercospora tiliae in Melanconis sensu lato as genera incertae sedis in Diaporthales. This taxonomic treatment was followed by Voglmayr et al. (2012), Voglmayr & Jaklitsch (2014) and Maharachchikumbura et al. (2015Maharachchikumbura et al. ( , 2016. ...
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... Although neither of the type species of Discostroma or Seimatosporium were included, Tanaka et al. (2011) used three species of Discostroma, including D. tostum and 11 species of Seimatosporium, to show that representatives of these genera form a monophyletic genus that should be regarded as Seimatosporium. Norphanphoun et al. (2015) added four more isolates of Seimatosporium, including one for the type species S. rosae, and also concluded that this genus was monophyletic. Given that Seimatosporium is the oldest name, has priority, has the greater number of species, and is most commonly used, this generic name should be used. ...
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In advancing to one scientific name for each fungus species, a number of name changes are required especially for plant-associated fungi. These include species names that are not in the correct genus. For example, the generic name Elsinoë is used for fungi causing scab diseases but a number of these species were described in the asexually typified genus Sphaceloma and must be placed in Elsinoë. In other cases species names were determined to be unrelated to the type species of the genus in which they are currently placed and are placed in a more appropriate genus. For each new name the history, rationale and importance of the name is discussed. The following new combinations are made: Acanthohelicospora aurea, A. scopula, Bifusella ahmadii, Botryobasidium capitatum, B. rubiginosum, Colletotrichum magnum, Crandallia acuminata, C. antarctica, Elsinoë arachadis, E. freyliniae, E. necator, E. perseae, E. poinsettiae, E. punicae, Entyloma gibbum, Harknessia farinosa, Passalora alocasiae, Protoventuria veronicae, Pseudocercosporella ranunculi, Psiloglonium stygium, Ramularia pseudomaculiformis, Seimatosporium tostum, Thielaviopsis radicicola combs. nov., and Venturia effusa.
... Tanaka et al. (2011) recognised Seimatosporium sensu lato as a monophyletic genus, although the type of Seimatosporium was not sequenced at that time. The generic type, S. rosae was subsequently epitypified and ex-epitype sequence data provided by Norphanphoun et al. (2015). Seimatosporium has been linked to Discostroma in several studies (Shoemaker & Müller 1964, Brockmann 1976, Nag Raj 1993, Okane et al. 1996, Hatakeyama & Harada 2004, Paulus et al. 2006, Hyde et al. 2011. ...
... In this study we introduce the sexual morph of Seimatosporium cornii based on analysis of combined LSU and ITS sequence data together with morphological characters following Tanaka et al. (2011) and Norphanphoun et al. (2015). Our isolate did not produce an asexual morph in culture. ...
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The sexual morph of Seimatosporium cornii, collected from dead stems of Cornus sanguinea in Arezzo, Italy, is reported in this paper. It was linked to S. cornii based on analysis of combined LSU and ITS sequence data. The sexual morph is characterized by minutely stromatic ascomata, cylindrical to clavate asci, with a J+, apical apparatus and 1–3-septate, fusiform ascospores. Seimatosporium cornii can be distinguished from the closely related species, Discostroma fuscellum, by the structure of the peridium, shape and septation of the ascospores and also its asexual morph. The sexual morph of S. cornii is reported from the same host and location as its asexual morph. We also provide data of SSU, TEF1-α and β-TUB genes of our strain, deposited in GenBank.
... The use of conidial morphology has often been considered an important criterion in species identification (Sutton 1980, Nag Raj 1993 and its value in taxonomy has been discussed in Norphanphoun et al. (2015). In our phylogenetic analysis (Fig. 1) Seimatosporium sensu lato groups into five sub-clades (Clades A-E). ...
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A new Seimatosporium species was collected from Quercus robur, in Germany. Morphological and phylogenetic analyses (maximum-parsimony and Bayesian analyses) of combined LSU and ITS datasets confirmed that our collection is distinct from other known species. It is introduced here as a new species, Seimatosporium quercina. The new species is compared with other similar Seimatosporium species and a description and illustrations are provided. A taxonomic key is provided to differentiate S. quercina from other morphologically similar species.