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Introduction to Fungi, Third Edition

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600 HETEROBASIDIOMYCETES<br />

21.3.1 Dacrymyces<br />

Orange gelatinous cushions about 1 5mm in<br />

diameter, so common on damp rotting wood,<br />

are the fructifications of D. stillatus (Fig. 21.3a).<br />

Close inspection with a hand lens reveals that<br />

the fruit bodies are of two kinds: soft, bright<br />

orange, hemispherical cushions and firmer, pale<br />

yellow, flatter structures. The bright orange<br />

cushions are conidial pustules which consist of<br />

hyphae whose tips are branched and fragment<br />

in<strong>to</strong> numerous dikaryotic arthroconidia (Fig.<br />

21.4c). The cells are packed with oil globules<br />

containing carotenoids. Such conidia are readily<br />

dispersed by rainsplash and are obviously similar<br />

in function <strong>to</strong> the splash-dispersed conidia of<br />

Nectria cinnabarina (see Plate 5d). The yellow<br />

flatter structures are basidial cushions which<br />

are attached centrally <strong>to</strong> the woody substratum.<br />

The surface layer is composed of clusters of<br />

forked basidia (Fig. 21.4b) which arise from<br />

dikaryotic hyphae. Each basidium forms two<br />

haploid basidiospores. After discharge, a basidiospore<br />

undergoes nuclear division and<br />

septation <strong>to</strong> give four cells. Depending on environmental<br />

conditions, each cell germinates by<br />

means of a monokaryotic haploid germ tube<br />

or by a short conidiophore (denticle). Conidia<br />

may also arise on older hyphae. They germinate<br />

<strong>to</strong> give monokaryotic hyphae. Dikaryotization<br />

occurs when two compatible monokaryotic<br />

hyphae fuse. Mossebo and Amougou (2001) have<br />

shown that the parenthesome and dolipore<br />

complex dissolve in order <strong>to</strong> facilitate passage<br />

of nuclei through the septum in the course of<br />

dikaryotization. Dacrymyces stillatus is heterothallic<br />

with a bifac<strong>to</strong>rial (tetrapolar) mating system.<br />

Cells of the secondary mycelium are usually but<br />

not unfailingly dikaryotic (Mossebo, 1998).<br />

21.3.2 Calocera<br />

At first sight the ubiqui<strong>to</strong>us cylindrical orange<br />

outgrowths of C. viscosa from coniferous logs<br />

(Plate 11g), or the smaller C. cornea from hardwood<br />

logs (Fig. 21.3b), could be mistaken for<br />

species of Clavaria. However, the gelatinous<br />

texture and the characteristically forked basidia<br />

(Fig. 21.5) place them in the Dacrymycetales, and<br />

this placement has been confirmed by molecular<br />

phylogenetic studies (Weiss & Oberwinkler, 2001).<br />

Ingold (1983b) has carefully observed the fate<br />

Fig 21.5 Calocera viscosa. (a) T.S. through hymenium with furcate basidia at different stages of development. (b) Freshly discharged<br />

basidiospores which are aseptate.The clear area in each spore shows the displacement of cy<strong>to</strong>plasmic contents by the single<br />

nucleus. (c) Two 24-hour-old basidiospores on tap-water agar. Each spore has produced two conidiophores bearing microconidia<br />

on denticles. (d) Direct germination of a basidiospore has given rise <strong>to</strong> monokaryotic hyphae which are forming microconidia.<br />

The septum dividing the spore in<strong>to</strong> two is clearly visible. (b d) <strong>to</strong> same scale.

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