Pleosporales - CBS - KNAW
Pleosporales - CBS - KNAW
Pleosporales - CBS - KNAW
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Fungal Diversity<br />
monoceras Alcorn nested within Pleosporaceae based on<br />
multigene phylogenetic analysis (Schoch et al. 2009;<br />
Plate 1).<br />
Syncarpella Theiss. & Syd., Annls mycol. 13: 631 (1915).<br />
Type species: Syncarpella tumefaciens (Ellis & Harkn.)<br />
Theiss. & Syd., Annls mycol. 13(5/6): 633 (1915).<br />
≡ Sphaeria tumefaciens Ellis & Harkn., J. Mycol. 2: 41<br />
(1886).<br />
Syncarpella was introduced by Theissen and Sydow<br />
(1915) as a genus of Montagnellaceae within Dothideales.<br />
A detailed description of S. tumefaciens can be seen in Barr<br />
and Boise (1989). Syncarpella was considered closely<br />
related to Leptosphaeria, and was treated as a synonym<br />
(Clements and Shear 1931). Syncarpella is characterized by<br />
its abundant globose, ovoid to turbinate ascomata with<br />
minute papillae which are seated on a common basal stroma<br />
and which are erumpent through fissures in the host tissues<br />
(Barr and Boise 1989). The peridium is thicker at the base,<br />
pseudoparaphyses are cellular, and asci are bitunicate,<br />
clavate to oblong with a furcate pedicel. Ascospores are<br />
pale brown to brown, oblong to narrowly obovoid, ends<br />
obtuse, transversely septate, smooth-walled. All these<br />
characters fit Cucurbitariaceae, where Barr and Boise<br />
(1989) transferred Syncarpella.<br />
Teichospora Fuckel, Jb. nassau. Ver. Naturk. 23–24: 160<br />
(1870) [1869–70].<br />
Type species: Teichospora trabicola Fuckel, Jb. nassau.<br />
Ver. Naturk. 23–24: 161 (1870) [1869–70].<br />
Teichospora was introduced by Fuckel (1870), and was<br />
typified by T. trabicola, with four more species included,<br />
i.e. T. brevirostris Fuckel, T. dura Fuckel, T. morthieri<br />
Fuckel and T. obducens (Schumach.) Fuckel. Only T.<br />
brevirostris and T. trabicola were kept in Teichospora<br />
(Barr 1987b). After studying the type specimens, Barr<br />
(1987b) indicated that Teichospora was different from<br />
Strickeria with Teichospora belonging to <strong>Pleosporales</strong>,<br />
and Strickeria closely related to Melanomma (Melanommatales).<br />
Currently, more than 250 names are included<br />
within Teichospora (http://www.mycobank.org, Jan/2011),<br />
but almost no molecular phylogenetic study has been<br />
conductedonthisgenus.<br />
Testudina Bizz., Atti Inst. Veneto Sci. lett., ed Arti, Sér. 6<br />
3: 303 (1885).<br />
Type species: Testudina terrestris Bizz., Fungi venet. nov.<br />
vel. Crit. 3: 303 (1885).<br />
Testudina terrestris is characterized by its reticulately<br />
ridged ascospores, which readily distinguish it from other<br />
genera of Zopfiaceae (Hawksworth 1979). The species is<br />
usually associated with other fungi, or on the wood of Abies?<br />
and Pinus or on the fallen leaves of Taxus in Europe<br />
(Hawksworth and Booth 1974; Hawksworth1979).<br />
Tetraplosphaeria Kaz. Tanaka & K. Hirayama, Stud.<br />
Mycol. 64: 177 (2009).<br />
Type species: Tetraplosphaeria sasicola Kaz. Tanaka & K.<br />
Hirayama, Stud. Mycol. 64: 180 (2009).<br />
Tetraplosphaeria was introduced by Tanaka et al. (2009)<br />
to accommodate bambusicolous fungi with immersed to<br />
erumpent, globose to subglobose and smaller (mostly<<br />
300 μm) ascomata. The peridium is thin, and is composed<br />
of thin-walled cells of textura angularis. The pseudoparaphyses<br />
are cellular, and asci are fissitunicate, 8-spored,<br />
cylindrical to clavate with short pedicels. Ascospores are<br />
narrowly fusoid, hyaline and surrounded with a sheath.<br />
Species of Tetraplosphaeria have Tetraploa sensu stricto<br />
anamorphic stage, which is quite unique in Tetraplosphaeriaceae<br />
(Tanaka et al. 2009).<br />
Tingoldiago K. Hirayama & Kaz. Tanaka, Mycologia 102:<br />
740 (2010).<br />
Type species: Tingoldiago graminicola K. Hirayama &<br />
Kaz. Tanaka, Mycologia 102(3): 740 (2010).<br />
Tingoldiago is a genus of freshwater ascomycetes characterized<br />
by flattened, globose, immersed to erumpent ascomata,<br />
and numerous cellular pseudoparaphyses (Hirayama et al.<br />
2010). Asci are fissitunicate and cylindrical, and ascospores<br />
are 1-septate, which usually turn 3-septate and pale brown<br />
when old, usually with a sheath (Hirayama et al. 2010).<br />
Based on both morphology and multigene phylogenetic<br />
analysis, Tingoldiago should be treated as a synonym of<br />
Lentithecium (Shearer et al. 2009a; Zhang et al. 2009a).<br />
Tremateia Kohlm., Volkm.-Kohlm. & O.E. Erikss., Bot.<br />
Mar. 38: 165 (1995).<br />
Type species: Tremateia halophila Kohlm., Volkm.-Kohlm.<br />
& O.E. Erikss., Bot. Mar. 38: 166 (1995).<br />
Tremateia was introduced as a facultative marine genus<br />
which is characterized by depressed globose, immersed<br />
ascomata, numerous and cellular pseudoparaphyses, fissitunicate<br />
and clavate asci, ellipsoid muriform ascospores,<br />
and a Phoma-like anamorph (Kohlmeyer et al. 1995).<br />
These characters point Tremateia to Pleosporaceae<br />
(Kohlmeyer et al. 1995). DNA sequence based phylogenies<br />
placed T. halophila as sister to Bimuria novae-zelandiae<br />
in Montagnulaceae (Schoch et al. 2009; Suetrong et al.<br />
2009).<br />
Triplosphaeria Kaz. Tanaka & K. Hirayama, Stud. Mycol.<br />
64: 186 (2009).<br />
Type species: Triplosphaeria maxima Kaz. Tanaka & K.<br />
Hirayama, Stud. Mycol. 64: 188 (2009).<br />
Triplosphaeria was introduced as a bambusicolous genus<br />
characterized by immersed ascomata, numerous cellular