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Introduction to Fungi, Third Edition

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426 HYMENOASCOMYCETES: PEZIZALES (OPERCULATE DISCOMYCETES)<br />

have shown that ascosporogenesis resembles<br />

that found in most other Euascomycetes, but<br />

instead of being delimited by the invagination of<br />

an ascus vesicle the ascospores become delimited<br />

individually by vesicles formed by material<br />

derived from lomasomes or from invaginations<br />

of the ascus plasma membrane (Berta & Fusconi,<br />

1983).<br />

At first, the developing ascocarp is attached<br />

by hyphal connections <strong>to</strong> a host tree, i.e. it grows<br />

symbiotically. Eventually it breaks free and<br />

continues <strong>to</strong> develop independently during a<br />

saprotrophic phase of growth. In T. melanosporum,<br />

tufts of hyphae extend in<strong>to</strong> the surrounding soil<br />

from the pyramidal scales on the outside of<br />

the peridium. Application of radioactive tracers<br />

(e.g.<br />

32 PO 4 ,<br />

3 H 2 O and 14 C-labelled mannose) <strong>to</strong><br />

these hyphae is rapidly followed by the appearance<br />

of radioactive material in the inner portions<br />

of the gleba and especially in the fertile<br />

veins (i.e. the dark regions of the ascocarp<br />

interior; see Fig. 14.7a) at rates and in patterns<br />

which could not be accounted for by simple diffusion<br />

(Barry et al., 1994, 1995). This finding<br />

and reports that fruit bodies of truffles may be<br />

found a considerable distance away from living<br />

tree roots suggest that mature ascocarps may<br />

be au<strong>to</strong>nomous and can obtain water and nutrients<br />

directly from the soil, from decaying<br />

roots and faecal deposits from the soil fauna<br />

(Callot, 1999).<br />

The species of Tuber which have been investigated<br />

have a wide mycorrhizal host range,<br />

including Angiosperms and some Gymnosperms.<br />

The host ranges of four species of Tuber are<br />

shown in Table 14.2.<br />

14.7.3 Truffle collecting<br />

The truffles of greatest commercial value are<br />

Tuber melanosporum (the black truffle of Périgord)<br />

and T. magnatum (the white truffle of Piedmont),<br />

which can command prices of up <strong>to</strong> E2000 kg 1<br />

in Continental Europe. Several other species<br />

are also traded. The only common British truffle<br />

which can be used for culinary purposes is<br />

T. aestivum. Périgord and Piedmont truffles are<br />

most abundant in Southern Europe (France,<br />

Spain and Italy) within latitudes 40° and 50°<br />

North in well-drained calcareous soils (Callot,<br />

1999). Both are collected with the aid of pigs<br />

and dogs trained <strong>to</strong> detect them by smell.<br />

The Périgord truffle can also be detected by<br />

the presence of a ‘burnt’ ring-like zone (brûlé)<br />

Table14.2. Host species relationships of four species of Tuber. The main hosts are indicated by black symbols.<br />

Marks in brackets indicate the formation of mycorrhiza with some, but not all members of the host genus<br />

tested. Data summarized from Giovannetti et al. (1994).<br />

Tubermagnatum T.melanosporum T.aestivumgroup T. albidum group<br />

Alnus cordata <br />

Carpinus betulus <br />

Castanea sativa <br />

Cistus (2 spp.) <br />

Corylus avellana <br />

Fagus sylvatica <br />

Ostrya carpinifolia <br />

Populus (2 spp.) <br />

Quercus (6 spp.) () <br />

Salix (2 spp.) <br />

Tilia (3 spp.) <br />

Abies alba <br />

Cedrus (2 spp.) <br />

Pinus (7 spp.) () () ()

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