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Bulletin of the British Museum (Natural History)

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LICHEN GENUS MICAREA IN EUROPE 67<br />

mould (e.g. in <strong>the</strong> Metacapnodiaceae) which have three hyphomycetous anamorphs (Hughes<br />

1972, 1976).<br />

The main distinguishing features <strong>of</strong> <strong>the</strong> three conidium types found in Micarea are as follows<br />

(see Figs 37-52 for example): Microconidia, narrowly cylindrical or narrowly fusiform, aseptate,<br />

eguttulate and not constricted in <strong>the</strong> middle, mostly in <strong>the</strong> range 3-8x0-5-1 /Am; produced in<br />

small immersed or ± sessile pycnidia, mostly c. 20-60 /xm diam. Mesoconidia, variable in shape,<br />

e.g. cylindrical, oblong, ovoid-oblong or obovoid-oblong, aseptate, <strong>of</strong>ten biguttulate and (or)<br />

slightly constricted in <strong>the</strong> middle; produced in small to large, immersed, sessile or stalked<br />

pycnidia. All conidia found in stalked pycnidia are included here. Macroconidia, mostly fihform<br />

or curved and <strong>of</strong>ten septate, or heUcoid and septate (M. subnigrata (p. 183)); produced in<br />

medium-sized to large (<strong>of</strong>ten up to 200 jxm diam or more) pycnidia. Also included here are <strong>the</strong><br />

large, aseptate, eguttulate, oblong-ellipsoid conidia produced by <strong>the</strong> sporodochia <strong>of</strong> M. adnata.<br />

In all cases no single pycnidium has been found to contain more than one conidium type. A<br />

few specimens <strong>of</strong> M. denigrata and M. nitschkeana have been found with all three anamorphs on<br />

<strong>the</strong> same thallus; but such occurrences are rare and it is more usual to find just one or two <strong>of</strong><br />

<strong>the</strong>m. A few species (e.g. M. assimilata, M. crassipes, and M. incrassata appear to have only one<br />

anamorphic state, with conidia somewhat intermediate between microconidia and mesoconidia<br />

as defined above; thus <strong>the</strong> assignment <strong>of</strong> <strong>the</strong>ir conidia to one or o<strong>the</strong>r <strong>of</strong> <strong>the</strong>se types (Table 1)<br />

must be considered tentative. The distinction between <strong>the</strong> three conidium types (especially<br />

micro- and mesoconidia) is most obvious when two or three <strong>of</strong> <strong>the</strong>m occur on <strong>the</strong> same thallus.<br />

The use <strong>of</strong> <strong>the</strong> terms 'micro-', 'meso-' and 'macroconidia' are here apphed solely to <strong>the</strong> conidium<br />

types found in Micarea - <strong>the</strong>y may not necessarily be analogous to <strong>the</strong>ir use in o<strong>the</strong>r lichenized or<br />

non-lichenized fungi. Table 1 indicates <strong>the</strong> conidium type(s) known for each <strong>of</strong> <strong>the</strong> European<br />

species <strong>of</strong> Micarea, and from this a numerical summary <strong>of</strong> <strong>the</strong> various known combinations is as<br />

follows:<br />

Combination <strong>of</strong> conidium types Number <strong>of</strong> species<br />

(anamorphs) (holomorphs)<br />

Micro- -I- meso- -I- macro- 3<br />

Micro- + meso- 10<br />

Micro- -I- macro- 5<br />

Meso- -I- macro- 1<br />

Micro- only 6<br />

Meso- only<br />

Macro- only<br />

14<br />

Anamorph(s) unknown 6<br />

The role <strong>of</strong> each <strong>of</strong> <strong>the</strong> conidium types is as yet unknown. Vobis (1977) obtained successful<br />

germination and subsequent growth <strong>of</strong> mycelium from <strong>the</strong> macroconidia <strong>of</strong> Lecanactis abietina,<br />

but was unable to germinate <strong>the</strong> microconidia <strong>of</strong> <strong>the</strong> same species. His results suggest that <strong>the</strong><br />

former may well act as asexual propagules, and <strong>the</strong> latter as spermatia in sexual reproduction. It<br />

seems most likely to me that <strong>the</strong> microconidia oi Micarea species are spermatia. As to whe<strong>the</strong>r or<br />

not <strong>the</strong>y are essential components <strong>of</strong> <strong>the</strong> sexual reproductive process is much less certain; 21 <strong>of</strong><br />

<strong>the</strong> treated species are not known to produce microconidia.<br />

The role <strong>of</strong> conidia as asexual propagules is still a matter <strong>of</strong> much debate and speculation<br />

among lichenologists, but such a role (at least in certain cases) can be inferred from <strong>the</strong> fact that a<br />

few crustose species (e.g. Lecanactis subabietina and an undescribed Bacidia) are not known to<br />

have apo<strong>the</strong>cia or vegetative diaspores (i.e. soredia, isidia, etc.) but always have numerous<br />

pycnidia. To such examples can be added <strong>the</strong> numerous crustose lichens whose apo<strong>the</strong>cia are<br />

known, but which commonly occur as sterile populations with numerous pycnidia, e.g.<br />

Anisomeridium juistense (macroconidial state), Arthonia phaeobaea, A. spadicea, Bacidia<br />

arnoldiana, B. carneoglauca, B. trachona, Cliostomum graniforme, C. griffithii, Lecanactis<br />

abietina, Lecidea erratica, Opegrapha niveoatra, O. vermicellifera, and O. vulgata. This last<br />

group also includes Micarea botryaides, M. denigrata, M. misella, M. pycnidiophora, and M.<br />

stipitata, all <strong>of</strong> which commonly occur with abundant mesoconidia-containing pycnidia and few<br />

(if any) mature apo<strong>the</strong>cia.

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