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Pleosporales - CBS - KNAW

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Fungal Diversity<br />

Anamorph: Pycnidia typical of Stagonospora (Sphaeropsidales),<br />

“scattered,arisingsinglybothonthehostandinpure<br />

culture, in culture generally surrounded by an envelope of<br />

mycelial hyphae, numerous, immersed on the host, but nearly<br />

superficial in culture, subglobose to slightly applanate, black,<br />

150–250 μm diam., with a central slightly papillate ostiole,<br />

lacking a distinct neck; walls mainly 15–20 μm thick,<br />

composed of three to six layers of pseudoparenchymatous<br />

cells, the outermost layers dark brown and inner pale brown to<br />

hyaline cells somewhat compressed radially, very variable in<br />

size, cells of the outer layers mainly 7–12 μm long×4–6 μm<br />

wide in vertically section and 10–12 μm diam. in surface<br />

view, wall not or only slightly thicked near the ostiole.<br />

Conidiogenous cells lining the inner surface of the pycnidial<br />

cavity, holoblastic, minute and difficult to distinguish from the<br />

pseudoparenchymatous cells with which they are mixed,<br />

mammiform with a flattened apex, hyaline, smooth walled,<br />

about 4–6 μm tall and 4–6 μm wide. Conidia copiously<br />

produced, ellipsoid, with somewhat truncated ends, hyaline,<br />

smooth walled, (2-)3 septate, not or slightly constricted at the<br />

septa, often guttulate, rather thin walled, (21-)24–28(−34)<br />

μm×7–8.5(−11.5) μm” (from Kaiser et al. 1979).<br />

Material examined: KENYA, near Nairobi, on leaves of<br />

Saccharum officinarum L.; 24 Aug. 1977; leg. W.J. Kaiser<br />

(IMI 215888, holotype).<br />

Notes<br />

Morphology<br />

Saccharicola was separated from Leptosphaeria as a new<br />

genus based on its Stagonospora anamorph and its biotrophic<br />

habitat in leaves of sugar cane, and two species were<br />

included, i.e. Saccharicola bicolor and S. taiwanensis (J.M.<br />

Yen & C.C. Chi) O.E. Erikss. & D. Hawksw. (Eriksson and<br />

Hawksworth 2003). Saccharicola is characterized by its<br />

parasitic habitat on monocots, small ascomata, bitunicate<br />

asci, presence of pseudoparaphyses as well as its 3-septate<br />

ascospores (Eriksson and Hawksworth 2003).<br />

Phylogenetic study<br />

Based on the limited phylogenetic analysis of SSU<br />

sequences, Saccharicola is considered to be closely related<br />

to Massarina eburnea, the generic type of Massarina<br />

(Eriksson and Hawksworth 2003). Thus, Saccharicola was<br />

assigned to Massarinaceae, which includes Keissleriella,<br />

Massarina and Saccharicola (Eriksson and Hawksworth<br />

2003).<br />

Concluding remarks<br />

Based on the parasitic habitat on monocots and its small<br />

ascomata and Stagonospora (or Cercospora? for S. taiwanensis,<br />

see Eriksson and Hawksworth 2003; Shoemaker<br />

and Babcock 1989b) anamorph, Saccharicola seems more<br />

similar to Pleosporineae. Further molecular study is needed<br />

for confirmation.<br />

Salsuginea K.D. Hyde, Bot. Mar. 34: 315 (1991). (<strong>Pleosporales</strong>,<br />

genera incertae sedis)<br />

Generic description<br />

Habitat marine, saprobic. Ascomata large, solitary, fusoid,<br />

conical or subglobose, with or without a flattened base,<br />

immersed under a darkened clypeus, papillate, ostiolate.<br />

Peridium thin, composed of round cells (in cross section) at<br />

sides, fusing at the top with the clypeus, thin at the base.<br />

Hamathecium of dense, long trabeculate pseudoparaphyses,<br />

anastomosing, embedded in mucilage. Asci 8-spored, bitunicate,<br />

fissitunicate, clavate to cylindro-clavate, pedunculate,<br />

with a large ocular chamber and conspicuous apical ring.<br />

Ascospores uniseriate, obovoid, brown to black, with hyaline<br />

apical germ pores, 1-septate, constricted at the septum, dark<br />

brown with paler apical cells, lacking sheath, smooth.<br />

Anamorphs reported for genus: none.<br />

Literature: Hyde 1991a; Suetrong et al. 2009.<br />

Type species<br />

Salsuginea ramicola K.D. Hyde, Bot. Mar. 34: 316 (1991).<br />

(Fig. 85)<br />

Ascomata 1040–2600 μm high×455–1430 μm diam.,<br />

solitary, fusoid, conical or subglobose, with or without a<br />

flattened base, immersed under a darkened clypeus, papillate,<br />

ostiolate, ostiole rounded (Fig. 85a). Peridium up to 39 μm<br />

thick, composed of round cells (in cross section) at sides,<br />

fusing at the top with the clypeus, thin at the base (Fig. 85b).<br />

Hamathecium of dense, long trabeculate pseudoparaphyses,<br />

1–2 μm broad, anastomosing, embedded in mucilage. Asci<br />

440–512×29–34 μm, 8-spored, bitunicate, fissitunicate,<br />

clavate to cylindro-clavate, pedunculate, with a large ocular<br />

chamber and conspicuous apical ring (Fig. 85c and e).<br />

Ascospores 59–72×24–30 μm, uniseriate, obovoid, brown to<br />

black, with hyaline apical germ pores, 1-septate, constricted<br />

at the septum, dark brown with paler apical cells, lacking<br />

sheath, smooth (Fig. 85d and f).<br />

Anamorph: none reported.<br />

Material examined: THAILAND, Ranong mangrove,<br />

Aegiceras corniculatum (L.) Blanco., Oct. 1988, leg. & det.<br />

K.D. Hyde (BRIP 17102, holotype).<br />

Notes<br />

Morphology<br />

Salsuginea was introduced to accommodate the mangrove<br />

fungus, S. ramicola, which is characterized by large,<br />

immersed, ostiolate and papillate ascomata under a clypeus,

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