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Fungi Fimicoli Italici - Mycosphere-online journal

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1999), and it has exceptionally isolated from<br />

dung (Cailleux 1971a).<br />

Rodentomyces Doveri, Pecchia, Sarrocco &<br />

Vannacci (Table 34)<br />

Refer to Doveri et al. (2010a) for the<br />

protologue of Rodentomyces gen. nov., R.<br />

reticulatus sp. nov.<br />

Sordariomycetes – Hypocreomycetidae –<br />

Melanosporales – Ceratostomataceae<br />

Melanospora Corda (Table 35)<br />

The genus Melanospora is usually<br />

isolated from decaying vegetables and soil, or<br />

detected in association with other fungi, also on<br />

dung, possibly behaving as a mycoparasite<br />

(Cannon & Hawksworth 1982). Coprophilous<br />

collections of Melanospora are unusual (Faurel<br />

& Schotter 1965, Calviello 1976, Lorenzo<br />

1990, Richardson 2004a, 2008b), and I have<br />

rarely found records of M. brevirostris (Hansen<br />

et al. 1998, Delgado Avila et al. 2001b, Moyne<br />

et Petit 2006) and M. zamiae (Seth 1968,<br />

Lorenzo 1992, Valldosera & Guarro 1992,<br />

Piontelli et al. 2006) directly from dung.<br />

Persiciospora P.F. Cannon & D. Hawksw.<br />

(Table 36)<br />

Mine and Eriksson's (2009) are the only<br />

three collections of Persiciospora known from<br />

dung, where it possibly behaves as a<br />

mycoparasite (Cannon & Hawksworth 1982).<br />

“Sordaria” minima (Table 37)<br />

“Sordaria” minima is possibly a<br />

Melanospora sp. (Lundqvist pers. comm.), but<br />

it has not been recombined yet in this genus.<br />

Like some Melanospora spp., this rare species<br />

has been found on dung in association with<br />

other fungi, particularly with Thelebolus (Lund<br />

qvist pers. comm.). Besides mine, a few other<br />

collections of S. minima have been recorded<br />

from various kinds of dung (Massee & Salmon<br />

1901, Larsen 1971, Richardson 1998, 2004b,<br />

Moyne & Petit 2006, Welt & Heine 2007).<br />

Sordariomycetes – Hypocreomycetidae –<br />

Microascales – Microascaceae<br />

Enterocarpus Locq.–Lin. (Table 38)<br />

362<br />

See the taxonomic part of this work,<br />

under Lophotrichus bartlettii, for discussion on<br />

Enterocarpus grenotii.<br />

Kernia Nieuwl. (Table 39)<br />

K. nitida is the commonest species of this<br />

genus, found by me in Italy on a variety of<br />

dungs with low frequency of occurrence in<br />

damp chambers (1%). Like other Kernia spp.<br />

and many Microascaceae with a cellulytic and<br />

proteolytic activity (Lumley et al. 2000), it has<br />

been found on a variety of substrates and<br />

dungs, particularly (24% of fimicolous records<br />

worldwide) on sheep dung (Tóth 1965, 1967,<br />

Udagawa 1980, Guarro Artigas 1983,<br />

Valldosera 1991, Richardson 2004a).<br />

Lophotrichus R.K. Benj. (Table 40)<br />

See the taxonomic part of this work,<br />

under Lophotrichus bartlettii, for discussion on<br />

Lophotrichus.<br />

Pithoascus Arx (Table 41)<br />

See the taxonomic part of this work,<br />

under Pithoascus intermedius, for discussion<br />

on Microascaceae, Pithoascus, and Microascus.<br />

Sphaeronaemella P. Karst. (Table 42)<br />

Out of five recognised species of<br />

Sphaeronaemella (Kirk et al. 2008), only one,<br />

S. fimicola, has been isolated from dung, where<br />

it can behave as a facultative mycoparasite<br />

(Cain & Weresub 1957, Weber & Webster<br />

1997, 1998). S. fimicola has a wide substrate<br />

tolerance, carnivore dung included (Marchal<br />

1891, Pease 1948, Cain 1957), but it prefers<br />

leporine (32% of several records worldwide)<br />

(Massee & Salmon 1902, Dennis 1981) and<br />

cervine (26%) (Cannon & Hawksworth 1982,<br />

Lundqvist 1989) dung.<br />

Sordariomycetes – Sordariomycetidae –<br />

Sordariales – Chaetomiaceae<br />

Chaetomidium (Zopf) Sacc. (Table 43)<br />

See the taxonomic part of this work,<br />

under Chaetomidium fimeti, for discussion on<br />

the genus Chaetomidium, C. megasporum, and<br />

C. fimeti.

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