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Pleosporales - CBS - KNAW

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Fungal Diversity<br />

ascospores of Platystomum have both transverse and<br />

vertical septa (Barr 1990a, b; ChestersandBell1970).<br />

However, the boundary between Lophiostoma and Platystomum<br />

is not clear (Chesters and Bell 1970). Holm and<br />

Holm (1988) treated Platystomum as a synonym of<br />

Lophiostoma, and concurrently, the Platystomaceae<br />

should be treated as a synonym of Lophiostomataceae.<br />

Based on a phylogenetic analysis, however, the generic<br />

type of Platystomum (P. compressum) separated from<br />

other species of Lophiostoma, and nested with the clade of<br />

Platystomaceae (Mugambi and Huhndorf 2009b) which<br />

may be closely related to species in the Testiduniaceae<br />

(Plate 1).<br />

Polyplosphaeria Kaz. Tanaka & K. Hirayama, Stud.<br />

Mycol. 64: 192 (2009).<br />

Type species: Polyplosphaeria fusca Kaz. Tanaka & K.<br />

Hirayama, Stud. Mycol. 64: 193 (2009).<br />

Polyplosphaeria is characterized by globose ascomata<br />

surrounded by numerous brown hyphae and a reddish<br />

pigment on the host surface around the ascomata (Tanaka et<br />

al. 2009). Asci are cylindro-clavate with fissitunicate<br />

dehiscence and ascospores are narrowly fusoid surrounded<br />

by a sheath. The anamorph is Piricauda-like (Tanaka et al.<br />

2009). The cylindro-clavate asci, narrowly fusoid ascospores<br />

as well as its thin and numerous pseudoparaphyses are<br />

comparable with those of Massarina sensu lato, especially<br />

Lentithecium (Zhang et al. 2009a). The terrestrial and<br />

bambusicolous habitat of Polyplosphaeria and Piricauda<br />

anamorph readily distinguishes the genus from Lentithecium.<br />

Pontoporeia Kohlm., Nova Hedwigia 6: 5 (1963).<br />

Type species: Pontoporeia biturbinata (Durieu & Mont.)<br />

Kohlm., Nova Hedwigia 6: 5 (1963)<br />

≡ Sphaeria biturbinata Durieu & Mont., Flora Algéricae<br />

1: 497 (1849).<br />

Pontoporeia was introduced by Kohlmeyer in 1963,<br />

and is monotypified by P. biturbinata. Pontoporeia was<br />

treated as a synonym of Zopfia (Malloch and Cain 1972),<br />

which is followed by Hawksworth and Booth (1974).<br />

Based on its asci originating at the periphery of the<br />

subglobose locus, filaments occupying the center of the<br />

ascocarps, the irregular peridial structure, the ascospores<br />

having 2-layered walls with a germ pore at each end and<br />

its marine habitat, Pontoporeia was kept as a separate<br />

genus within Pleosporaceae (Kohlmeyer and Kohlmeyer<br />

1979). A DNA based phylogeny placed an isolate on a<br />

long branch in relationship with other marine species,<br />

Halotthia posidoniae and Mauritiana rhizophorae, but a<br />

familial placement awaits further resolution (Suetrong et<br />

al. 2009).<br />

Pseudotrichia Kirschst., Annls mycol. 37: 125 (1939).<br />

Type species: Pseudotrichia stromatophila Kirschst., Annls<br />

mycol. 37: 125 (1939).<br />

Pseudotrichia can be distinguished from Byssosphaeria,<br />

Herpotrichia and Lojkania by its lacking of subiculum,<br />

larger ascomata usually with compressed apices, the<br />

peripheral arrangement of asci and trabeculate pseudoparaphyses<br />

(Barr 1984). Phylogenetic study of strains Pseudotrichia<br />

mutabilis and some Herpotrichia species indicated<br />

that these species are closely related, and both nested within<br />

Melanommataceae (Mugambi and Huhndorf 2009b). But in<br />

this study, Pseudotrichia guatopoensis nested in the<br />

Testudinaceae (or Platystomaceae) (Plate 1). The types of<br />

both Herpotrichia and Pseudotrichia need recollecting,<br />

redescribing and epitypifying in order to stabiles the use of<br />

these generic names and clarify their familial status.<br />

Pseudoyuconia Lar.N. Vassiljeva, Nov. sist. Niz. Rast. 20:<br />

71 (1983).<br />

Type species: Pseudoyuconia thalictri (G. Winter) Lar. N.<br />

Vassiljeva [as ‘thalicti’], Nov. sist. Niz. Rast. 20: 71 (1983).<br />

≡ Leptosphaeria thalictri G. Winter, Hedwigia 10: 40<br />

(1872).<br />

Pseudoyuconia was introduced by Vassiljeva (1983), and<br />

was monotypified by P. thalictri. Currently, Pseudoyuconia<br />

is included in Pleosporaceae (Lumbsch and Huhndorf<br />

2010).<br />

Pyrenophora Fr., Summa veg. Scand., Section Post.<br />

(Stockholm): 397 (1849).<br />

Type species: Pyrenophora phaeocomes (Rebent.) Fr.,<br />

Summa veg. Scand., Section Post. (Stockholm): 397<br />

(1849).<br />

≡ Sphaeria phaeocomes Rebent., Prodr. fl. neomarch.<br />

(Berolini): 338 (1804).<br />

Pyrenophora is characterized by immersed, erumpent to<br />

nearly superficial ascomata, indefinite pseudoparaphyses,<br />

clavate to saccate asci usually with a large apical ring, and<br />

muriform terete ascospores. Morphologically, the terete<br />

ascospores of Pyrenophora can be readily distinguished<br />

from Clathrospora and Platyspora. The indefinite pseudoparaphyses<br />

and smaller ascospores of Pyrenophora can be<br />

readily distinguished from those of Pleospora (Sivanesan<br />

1984). Based on both morphology and molecular phylogeny,<br />

Pyrenophora is closely related to Pleosporaceae<br />

(Zhang et al. 2009a).<br />

Rechingeriella Petr., in Rechinger et al. Annln naturh. Mus.<br />

Wien 50: 465 (1940).<br />

Type species: Rechingeriella insignis Petr., Annln naturh.<br />

Mus. Wien, Ser. B, Bot. Zool. 50: 465 (1940).<br />

Rechingeriella is characterized by its erumpent to<br />

superficial, cleistothecioid ascomata and thin, branching<br />

pseudoparaphyses (Hawksworth and Booth 1974). Asci are

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