Pseudohalonectria fagicola R.H. Perera, E.B.G. Jones & K.D. Hyde, 2016
publication ID |
https://doi.org/ 10.11646/phytotaxa.278.2.2 |
persistent identifier |
https://treatment.plazi.org/id/E0216A53-A068-FFAB-30E4-7B11FAB7F7CD |
treatment provided by |
Felipe |
scientific name |
Pseudohalonectria fagicola R.H. Perera, E.B.G. Jones & K.D. Hyde |
status |
sp. nov. |
Pseudohalonectria fagicola R.H. Perera, E.B.G. Jones & K.D. Hyde View in CoL , sp. nov. ( Fig. 3a–p View FIGURE 3 ),
Index Fungorum: IF552161, Facesoffungi number: FoF 02231
Etymology:—In reference to the host genus Fagus , and cola meaning loving.
Holotype:— MFLU 16-1085 View Materials
Saprobic on beech cupules ( Fagus sylvatica L.). Sexual morph: Ascomata 275–690 × 225–500 μm, solitary to less commonly aggregated,immersed with a protruding neck,globose to depressed globose,greenish yellow at first,becoming darkened with age, rostrate. Neck 90–390 × 70–160 μm, conical, composed of parallel hyphae, outer hyphae outwardly directed, subglobose with enlarged ends, greenish yellow, periphysate. Peridium 9–32 μm wide, membranous, 5–12 cell layers, inner layer composed pale yellow cells of textura angularis, outer cells pseudoparenchymatic, composed of darkened yellow, laterally compressed cells of textura angularis. Paraphyses 62–116 × 3.1–5.6 μm, 1–4-septate, wide at base, tapering towards the apex, thin-walled, attached to ascogenous hyphae. Asci 83–104 × 8.8–11 μm diam. (x = 93 × 10 μm, n = 30), 8-spored, unitunicate, cylindrical, straight or sigmoidal, separating at the basal septum from ascogenous hyphae, thimble-shaped apical apparatus, J-. Ascospores 26–33 × 3.9–5.1 μm diam. (x = 29 × 4.4 μm, n = 30), 4–6 (–7)-septate, overlapping uniseriate to biseriate, pale brown, pink/orange in mass, ellipsoidal, straight to curved, constricted or not-constricted at the septa, after discharge accumulating in a mass at the neck opening. Asexual morph: Undetermined.
Culture characters:—Slow growing, reaching 3 cm diam. within 21 days incubation on PDA, at 16° C, circular, effuse, with regular margin, yellowish-green in center and hyaline towards the margin from above; reverse yellow green to brown.
Material examined:— UK, Hampshire, Bishops Waltham, slightly anoxic, stagnant water, on beech cupules ( Fagus sylvatica L.), 3 June 2015, E. B. G. Jones, GJ 177b ( MFLU 16-1085, holotype, ibid. ( GZ, isotype), ex-type living culture, MFLUCC 15-1117, GZCC.
Notes:— Pseudohalonectria fagicola forms a separate clade (100% ML /PP) within the genus Pseudohalonectria as a sister taxon ( Fig. 2 View FIGURE 2 ) and shares some common characteristics, but differs in that it generally has smaller asci and ascospores. In P. lignicola asci (90–132 × 11–17.54 μm) and ascospores (38.4–74.8 × 3.5–6.5 μm) are larger. Pseudohalonectria fagicola is characterized by ellipsoidal 5–6(–7)-septate ascospores, while P. lignicola has 5–11 septa and cylindrical ascospores ( Shearer 1989). Although the shape of the ascospores of P. fagicola is similar to P. lutea , they are smaller than ascospores of P. lutea (48–68 × 4.8–8.4 μm) ( Shearer 1989). Pseudohalonectria fagicola differs from P. hampshirensis in its smaller ascomata. Pseudohalonectria hampshirensis has 0–3–4-septate, fusiform ascospores, while P. fagicola has 5–6(–7), ellipsoidal ascospores. Morphologically P. fagicola differs from other Pseudohalonectria species in the size of its ascomata, asci, ascospores and ascospore septation ( Table 2).
L |
Nationaal Herbarium Nederland, Leiden University branch |
PDA |
Royal Botanic Gardens |
C |
University of Copenhagen |
E |
Royal Botanic Garden Edinburgh |
B |
Botanischer Garten und Botanisches Museum Berlin-Dahlem, Zentraleinrichtung der Freien Universitaet |
G |
Conservatoire et Jardin botaniques de la Ville de Genève |
MFLU |
Mae Fah Laung University Herbarium |
MFLUCC |
Mae Fah Luang University Culture Collection |
ML |
Musee de Lectoure |
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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