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Introduction to Fungi, Third Edition

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SORDARIALES<br />

329<br />

Fig12.8 Neurospora crassa. (a) Ascus.<br />

(b) Ascospores showing ribbed surface.<br />

(c) Pro<strong>to</strong>perithecium showing projecting<br />

trichogyne. (d) Macroconidia from one-day-old<br />

culture. (e) Enlarged view of developing<br />

macroconidia. (f) Microconidia forming sticky<br />

clusters. (g) Enlarged view showing origin of<br />

microconidia. (a d,f) <strong>to</strong> same scale;<br />

(e,g) <strong>to</strong> same scale.<br />

and cohere in sticky masses (Beever et al., 1978).<br />

The pink colour of the conidia is due <strong>to</strong> the<br />

presence of a carotenoid pigment, neurosporoxanthin,<br />

which is stimulated <strong>to</strong> develop by<br />

light. The spores are formed in vast numbers.<br />

In labora<strong>to</strong>ries they can cause serious contamination<br />

of other cultures, partly because of the<br />

rapid growth of the mycelium (up <strong>to</strong> 5 mm h 1 ),<br />

and partly because macroconidia can develop<br />

in profusion beyond the rims of closed Petri<br />

dishes. In humid environments, the mycelium<br />

may grow through the cot<strong>to</strong>n wool plugs of testtube<br />

cultures and sporulate on the plugs. Shaw<br />

(1993) has reported that macroconidia formed on<br />

steamed pine logs in Queensland, Australia, are<br />

collected by honeybees in their pollen baskets.<br />

Cultures derived from a single ascospore also<br />

develop two other types of reproductive structure.<br />

In contrast <strong>to</strong> the large, dry, wind-dispersed<br />

macroconidia which are formed within 1 2 days,<br />

clumps of smaller, oval, uninucleate, sticky<br />

microconidia develop after about 12 15 days<br />

(Figs. 12.8f,g; Maheshwari, 1999). The conidiogenous<br />

cells from which the microconidia develop<br />

have been interpreted as reduced phialides. The<br />

microconidia are capable of slow and variable<br />

germination but function primarily as spermatia.<br />

Coiled ascogonia, terminated by long tapering<br />

trichogynes and surrounded at the base by<br />

hyphae, also develop (Fig. 12.8c). Such structures<br />

are termed pro<strong>to</strong>perithecia or bulbils and each<br />

often forms several trichogynes. In N. crassa and<br />

N. si<strong>to</strong>phila, no further development occurs in<br />

single ascospore cultures, i.e. each strain is selfincompatible.<br />

Incompatibility is controlled by a<br />

pair of mating type idiomorphs, A and a, and<br />

if two compatible strains are grown <strong>to</strong>gether in<br />

a Petri dish for a few days, microconidia of one

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