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Bulletin of the British Museum (Natural History)

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LICHEN GENUS MICAREA IN EUROPE 141<br />

richly branched, not or only slightly incrassate (to 1-8 /xm wide) and without closely adhering<br />

pigment (epi<strong>the</strong>cial pigment confined to surrounding gel-matrix). Hypo<strong>the</strong>cium c. 35-45 txm<br />

tall, but becoming much taller in markedly convex or tuberculate apo<strong>the</strong>cia, dilute straw- or<br />

fuscous-brown, pigment confined to gel matrix; hyphae interwoven, but becoming outwardly<br />

orientated towards <strong>the</strong> hymenium and excipulum, c. 0-8-1-5 /u,m wide; ascogenous hyphae with<br />

swollen cells, c. 2-6 /am wide. Excipulum distinct in young, moderately convex apo<strong>the</strong>cia, but<br />

reflexed and obscured in subglobose or tuberculate apo<strong>the</strong>cia, dilute fuscous brown (K— );<br />

hyphae radiating, branched and anastomosing, c. 0-5-1 -5 /u,m wide.<br />

Pycnidia not found.<br />

Chemistry: Thallus K-, C+ red, PD-I- red; apo<strong>the</strong>cia in section C-l- red; t.l.c: argopsin and<br />

gyrophoric acid.<br />

Observations: M. leprosula is characterized by its sterile or sparingly fertile, granular thallus<br />

composed <strong>of</strong> blue-grey (or brown-grey), fragile areolae which <strong>of</strong>ten dissolve (or become<br />

abraded) to form contrasting, yellowish green, sorediose patches. These characters are shared<br />

by <strong>the</strong> much rarer M. subleprosula, and <strong>the</strong> thalli <strong>of</strong> both react C+ red. However, M.<br />

subleprosula can be separated by <strong>the</strong> PD-I- yellow reaction <strong>of</strong> its thallus due to <strong>the</strong> presence <strong>of</strong><br />

alectorialic acid. When fertile M. subleprosula is found to have much larger, mostly 7-septate<br />

spores. M. leprosula is usually distinctive in <strong>the</strong> field (although material should always be<br />

checked with M. subleprosula in mind) but can easily be overlooked when it occurs on<br />

bryophytes on shaded rocks or trees, whence <strong>the</strong> thallus <strong>of</strong>ten lacks its characteristic bluish tinge<br />

and <strong>the</strong> areolae are thinly scattered. The species is usually sterile but fertile specimens are<br />

occasionally encountered, especially in sheltered (but not deeply shaded) situations, such as on<br />

boulders and old walls in woodland.<br />

Hedlund (1892) regarded M. leprosula as a variety <strong>of</strong> M. peliocarpa (q.v.) and <strong>the</strong> apo<strong>the</strong>cia<br />

<strong>of</strong> <strong>the</strong> two species are somewhat similar. However, those <strong>of</strong> M. leprosula exhibit several minor,<br />

yet significant, differences; spores tend to be slightly longer; apo<strong>the</strong>cia tend to be more<br />

markedly convex and more frequently tuberculate; hypo<strong>the</strong>cium and excipulum are dilutely<br />

pigmented with a dull brown pigment; and paraphyses never become thickened and pigmented<br />

at <strong>the</strong>ir apices. The two species also differ in several fundamental aspects <strong>of</strong> thallus morphology<br />

and chemistry. With regard to <strong>the</strong> production <strong>of</strong> argopsin and to <strong>the</strong> presence <strong>of</strong> a dull brown<br />

pigment in <strong>the</strong> excipulum and hypo<strong>the</strong>cium M. leprosula shows some affinity to M. lignaria var.<br />

lignaria, with which it <strong>of</strong>ten occurs. However, M. lignaria lacks gyrophoric acid, has usually<br />

longer and more septate spores, and somewhat stouter and only sparingly branched paraphyses.<br />

The areolae <strong>of</strong> M. leprosula and M. subleprosula differ from those <strong>of</strong> such species as M. lignaria,<br />

M. peliocarpa, and M. cinerea, in lacking an amorphous hyaline covering layer (see 'morpho-<br />

logy')-<br />

Habitat and distribution: M. leprosula is widely distributed in upland areas in <strong>the</strong> north and<br />

west <strong>of</strong> Britain, occurring at altitudes from about sea-level to at least 1100 m. It is found, usually<br />

on moribund bryophytes (e.g. Andraea spp. and Rhacomitrium spp.) on rocky ledges, boulders,<br />

and old walls, in exposed hilly areas, mountain sides or woodlands. Associated lichens noted<br />

amongst <strong>British</strong> collections include Arthrorhaphis citrinella, Baeomyces rufus, Belonia incar-<br />

nata, Cladonia cervicornis, C. coccifera, C. crispata, C. portentosa, C. squamosa, C. subcervicornis,<br />

Coelocaulon aculeatum, Lecidea granulosa, L. icmalea, Lepraria neglecta, Micarea<br />

lignaria, M. peliocarpa, and Vorarlbergia renitens. From Scotland I have seen two corticolous<br />

specimens, on trunks <strong>of</strong> Alnus and Betula; associated species present included Cladonia<br />

coniocraea, C. squamosa, Lecidea icmalea, Micarea melaena, and Platismatia glauca.<br />

There are two outlying localities in <strong>the</strong> lowlands <strong>of</strong> sou<strong>the</strong>rn England. In Dorset it occurs on<br />

waste heaps <strong>of</strong> slag clay with M. lignaria (q. v.); and in Kent it was found with M. peliocarpa on<br />

wood chips lying at <strong>the</strong> side <strong>of</strong> a woodland track in a chestnut (Castanea) coppice.<br />

M. leprosula is poorly recorded outside Britain, probably because it is so <strong>of</strong>ten sterile. To<br />

date, I have seen one specimen from Norway (Hordaland) and several collections from mid- and<br />

sou<strong>the</strong>rn Sweden. Fur<strong>the</strong>r south it seems to be well represented in <strong>the</strong> Alps, and I have seen one

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