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Pleosporales - CBS - KNAW

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Fungal Diversity<br />

Notes<br />

Morphology<br />

Herpotrichia was established by Fuckel (1868) comprising<br />

two species H. rhenana Fuckel and H. rubi Fuckel, but<br />

no generic type was assigned. Bose (1961) designatedH.<br />

rhenana as the lectotype species with H. rubi as a synonym.<br />

This proposal was followed by Müller and von Arx (1962)<br />

and Sivanesan (1971). Herpotrichia rubi was later assigned<br />

as the generic type (Holm 1979) as it was found to be validly<br />

published 2 years earlier than H. rhenana, thus having<br />

priority (Cannon 1982). However, Cannon (1982) reported<br />

that Sphaeria herpotrichoides Fuckel (1864, cited as a<br />

synonym of H. rhenana) was the earliest name. Thus he<br />

made a new combination as H. herpotrichoides (Fuckel) P.F.<br />

Cannon and cited H. rubi as the synonym. Herpotrichia rubi<br />

is maintained as the type of the genus (Holm 1979; Cannon<br />

1982), but the current name is H. herpotrichoides.<br />

Herpotrichia is a morphologically well studied genus<br />

(Barr 1984; Bose 1961; Müller and von Arx 1962;<br />

Pirozynski 1972; Samuels and Müller 1978; Sivanesan<br />

1971, 1984), and Herpotrichia sensu lato is characterized<br />

by having subglobose, pyriform to obpyriform ascomata<br />

and a peridium of textura angularis or comprising thickwalled<br />

polygonal cells with thin-walled hyaline cells<br />

towards the centre. Asci are clavate to cylindrical, 4–8-<br />

spored and ascospores are hyaline at first, becoming pale to<br />

dark brown, one to many septate, constricted or not at the<br />

septa and often surrounded by a mucilaginous sheath.<br />

Several morphologically distinct genera were synonymized<br />

under Herpotrichia using the above broad circumscription<br />

(Barr 1984; Müller and von Arx 1962; Sivanesan 1984). In<br />

particular, Barr kept Lojkania as a separate genus after<br />

studying its type material (Barr 1984, 1990a). Sivanesan<br />

(1984) was also of the opinion that Lojkania and Neopeckia<br />

were distinct genera as several of their characters differed.<br />

Byssosphaeria and Pseudotrichia have subsequently been<br />

assigned to Melanommataceae, Lojkania to Fenestellaceae<br />

and Neopeckia to Coccoideaceae (Barr 1984). Herpotrichia<br />

sensu stricto is represented by H. rubi and has erumpent to<br />

superficial ascomata or immersed in a subiculum, clavate to<br />

cylindrical, 4–8-spored, stalked asci with a conspicuous<br />

apical “nasse”, hyaline, 1-septate ascospores, usually becoming<br />

pale brown and several septate, constricted or not<br />

constricted at septa, usually surrounded by sheath (Sivanesan<br />

1984). Currently, about 90 species are included in this genus<br />

(http://www.indexfungorum.org/, 12/01/2009).<br />

Phylogenetic study<br />

Herpotrichia diffusa (Schwein.) Ellis & Everh., H.<br />

juniperi (Duby) Petr., H. herpotrichoides and H. macrotricha<br />

have been shown to have phylogenetic affinity with<br />

the generic types of Byssosphaeria schiedermayeriana,<br />

Melanomma pulvis-pyrius and Pleomassaria siparia, which<br />

had been assigned under Melanommataceae (Kruys et al.<br />

2006; Mugambi and Huhndorf 2009b; Schoch et al. 2006,<br />

2009; Zhang et al. 2009a). In this study, Pleomassaria<br />

siparia together with its closely related species of Prosthemium<br />

is kept in a separate family, viz Pleomassariaceae.<br />

Concluding remarks<br />

Even species under Herpotrichia sensu stricto (according<br />

to Sivanesan 1984) have diverse hosts (such as<br />

gymnosperms (H. coulteri (Peck) S.K. Bose and H. parasitica<br />

(R. Hartig) Rostr.) and angiosperms (H. diffusa and<br />

H. villosa Samuels & E. Müll.)) or substrates (like dead or<br />

living leaves, bark or decorticated wood) (Sivanesan 1984).<br />

Species of Herpotrichia sensu stricto are also reported from<br />

various locations such as Europe, Asia or America, and<br />

they have various life styles, e.g. parasitic, hyperparasitic or<br />

saprobic (Sivanesan 1984). Additional factors (like hosts or<br />

locations) may need to be considered in order to get a<br />

natural concept for Herpotrichia.<br />

Immotthia M.E. Barr, Mycotaxon 29: 504 (1987).<br />

(Teichosporaceae)<br />

Generic description<br />

Habitat terrestrial, hyperparasitic. Ascomata gregarious,<br />

globose, superficial, ostiolate, periphysate. Hamathecium<br />

of cellular pseudoparaphyses. Asci 8-spored, bitunicate,<br />

cylindrical, with a short pedicel. Ascospores 1-seriate,<br />

ellipsoidal, brown to reddish brown, 1-septate, constricted<br />

at the septum, smooth.<br />

Anamorphs reported for genus: none.<br />

Literature: Barr 1987a, 2002; Wang et al. 2004.<br />

Type species<br />

Immotthia hypoxylon (Ellis & Everh.) M.E. Barr, Mycotaxon<br />

29: 504 (1987). (Fig. 37)<br />

≡ Amphisphaeria hypoxylon Ellis & Everh., J. Mycol. 2:<br />

41 (1886).<br />

Ascomata gregarious, globose, superficial, ostiolate,<br />

periphysate, papillate (Fig. 37a). Hamathecium of cellular<br />

pseudoparaphyses, 2–2.5 μm broad, septate. Asci 60–82×<br />

7–9 μm, 8-spored, bitunicate, cylindrical, with a short<br />

pedicel (Fig. 37b, c and d). Ascospores 10–13×4.4–5.4 μm,<br />

1-seriate, ellipsoidal, brown to reddish brown, 1-septate,<br />

constricted at the septum, smooth (Fig. 37f, g and h)<br />

(adapted from Wang et al. 2004).<br />

Anamorph: none reported.<br />

Material examined: USA, Louisiana, Pointe a la<br />

Hache, on decaying wood, a branch of Carya oliviformis<br />

(Juglandaceae) lying on the ground in grass (parasitic on

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