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Introduction to Fungi, Third Edition

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DEVELOPMENT OF BASIDIA<br />

489<br />

Fig18.2 Some different kinds of basidia. (a) Longitudinally divided basidium of Exidiaglandulosa (Tremellales). (b) Tuning-fork type<br />

of basidium of Calocera viscosa (Dacrymycetales). (c) Transversely divided basidium of Auricularia auricula-judae (Auriculariales).<br />

(d) Germinating chlamydospore of Ustilago avenae (Ustilaginales). A transversely septate promycelium has developed and each<br />

segment is forming sporidia. (e) Germinating teliospore of Puccinia graminis (Uredinales). A transversely septate promycelium has<br />

developed and each segment is producing a single basidiospore.<br />

and has particularly large basidia. A detailed<br />

description of the process has been given by<br />

Corner (1948) for O. canarii. Ultrastructural<br />

studies have also been made on a range of<br />

fungi with holobasidia, e.g. the split-gill<br />

(Schizophyllum commune; Wells, 1965), the agarics<br />

Coprinus cinereus (McLaughlin, 1973, 1977, 1982)<br />

and Panellus stypticus (Lingle et al., 1992), the<br />

clavarioid fungus Clavicorona pyxidata (Berbee &<br />

Wells, 1989) and the bolete Boletus rubinellus<br />

(McLaughlin, 1973; Yoon & McLaughlin, 1979,<br />

1984).<br />

18.3.1 Cy<strong>to</strong>logical aspects<br />

In Oudemansiella radicata the basidium arises as<br />

the terminal cell of a hypha making up the gill<br />

tissue on the underside of the cap of the fruit body<br />

(basidiocarp). Basidia are packed tightly <strong>to</strong>gether<br />

in the hymenium at the surface of the gill. A<br />

basidium is at first filled with dense cy<strong>to</strong>plasm,<br />

but soon several small vacuoles appear near its<br />

base. Later these coalesce in<strong>to</strong> a single large<br />

vacuole at the base of the basidium and, by<br />

enlargement of this vacuole, cy<strong>to</strong>plasm is pushed<br />

<strong>to</strong>wards the apex of the basidium. A clear cap is<br />

differentiated at the tip and it is in this region<br />

that the sterigmata develop. Corner (1948) postulated<br />

that there must be four elastic areas in the<br />

upper part of the basidium wall from which<br />

the sterigmata extend. The wall of the upper part<br />

of the basidium consists of two layers, the outer of<br />

which is mucilaginous, the inner firmer. In the<br />

areas where the sterigmata are about <strong>to</strong> bulge<br />

out, a new layer of wall material is deposited<br />

between these two original layers. The outer<br />

mucilaginous layer of the basidial wall bursts<br />

and the apex of the sterigma grows out. It is<br />

surrounded by two wall layers, the inner of which<br />

is continuous with the inner wall layer of the<br />

basidium (Clémençon, 2004). Ultrastructural<br />

studies of Boletus rubinellus show that, in the<br />

region where the sterigmata appear, the basidial

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