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Bulletin of the British Museum (Natural History)

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140 BRIAN JOHN COPPINS<br />

forms <strong>of</strong> Scoliciosporum umbrinum with a well developed thallus, but that species has<br />

vermiform or sigmoid-curved spores. The phycobiont in M. intrusa and S. umbrinum appears to<br />

be <strong>the</strong> same; any future critical appraisal <strong>of</strong> <strong>the</strong> delimitation oi Scoliciosporum should seriously<br />

consider <strong>the</strong> generic disposition <strong>of</strong> M. intrusa.<br />

The pale orange, K+ purple-red pigment commonly found in <strong>the</strong> ascogenous hyphae, asci and<br />

spores has not been seen by me in any o<strong>the</strong>r Micarea, although it is conceivable that it is <strong>the</strong><br />

same, or similar, to <strong>the</strong> pigment found in <strong>the</strong> goniocysts <strong>of</strong> M. hedlundii {q. v.).<br />

Habitat and distribution: M. intrusa occurs on hard siliceous (igneous) rocks in communities<br />

referable to <strong>the</strong> Umbilicarietum cylindricae in its broad sense (James etal., 1977). In Nylander's<br />

protologue <strong>of</strong> Lecidea aphanoides it is said to occur on calcareous rock, but this is erroneous;<br />

application <strong>of</strong> 50% HNO3 to fragments <strong>of</strong> substratum from <strong>the</strong> holotype produced no efferves-<br />

cence. The formation <strong>of</strong> small patches amongst o<strong>the</strong>r crustose lichens indicates that M. intrusa<br />

may be, at least facultatively, parasitic. Such suggestions have been previously propounded by<br />

Magnusson (1942), Poelt (1958), and Wirth (1973), all <strong>of</strong> whom related its behaviour to that <strong>of</strong><br />

Lecanora intrudens and Lecidea furvella. In several collections, including <strong>the</strong> type <strong>of</strong> Lecidea<br />

intrusa, it occurs amongst <strong>the</strong> areolae <strong>of</strong> Huilia panaeola, but it is by no means confined to that<br />

'host'.<br />

From her studies on <strong>the</strong> island <strong>of</strong> Sotra in Hordaland, Norway, Miss L. Skjolddal informs me<br />

that M. intrusa occurs on sheltered, sunny, west or south-west facing exposures <strong>of</strong> gneiss and<br />

amphibolite, on steep surfaces or, in one case, on a ± horizontal surface. Miss Skjolddal kindly<br />

provided me with a list <strong>of</strong> associated species (Table 5).<br />

M. intrusa is probably widespread in areas <strong>of</strong> western Europe with exposed, hard, igneous<br />

rocks; however, it is a very inconspicuous species and records are wanting from many potential<br />

localities. I have seen material from sou<strong>the</strong>rn Scandinavia (several localities). North Norway<br />

(Finnmark), and <strong>the</strong> Grampian Mountains <strong>of</strong> Scotland. In addition, Wirth (1973) cites collections<br />

from France (Vosges) and West Germany (Schwarzwald).<br />

Exsiccata: Norrlin & Nyl. Herb. Lich. Fenn. 182 (BM).<br />

18. Micarea leprosula (Th. Fr.) Coppins & A. Fletcher<br />

(Figs 18, 53-54; Map 8)<br />

in Fletcher in Lichenologist 7: 111 (1975). - Bilimbia milliaria y leprosula Th. Fr. , Lich. Scand. 2: 382<br />

(1874). - Micarea violacea var. leprosula (Th. Fr.) Hedl. in Bih. K. svenska VetenskAkad. Handl. Ill, 18<br />

(3): 81, 92 (1892). - Bilimbia leprosula (Th. Fr.) H. Olivier in Bull. Geogr. bot. 21: 179 (1911). - Bacidia<br />

leprosula (Th. Fr.) Lettau in Hedwigia 52: 133 (1912). Type: Sweden, Uppsala, Witulfsberg [Wittuls-<br />

berg], 26 vi 1852, Th. M. Fries (UPS - lectotype! [t.l.c. : argopsin and gyrophoric acid]).<br />

Thallus effuse, superficial, <strong>of</strong> convex to subglobose areolae c. 100-350(-400) fxm diam; <strong>the</strong>se<br />

usually coalesce toward <strong>the</strong> centre <strong>of</strong> <strong>the</strong> thallus, whence <strong>the</strong>y may proliferate, producing<br />

secondary granular-areolae, such that <strong>the</strong> thallus becomes thicker (to c. 700 /xm thick). Areolae<br />

blue-grey or, more rarely, grey-brown, matt with a minutely roughened surface with white flecks<br />

(x50 lens); lower sides <strong>of</strong> ± globose areolae, and areolae in shaded situations, <strong>of</strong>ten unpigmented<br />

and greenish white. Areolae fragile and <strong>of</strong>ten breaking down or eroding to form<br />

sorediate patches with irregularly shaped soredial granules c. 20-50 /xm diam. Sections <strong>of</strong> intact<br />

areolae ecorticate and without an amorphous hyaline covering layer; outermost hyphae <strong>of</strong>ten<br />

coloured with greenish or brownish pigment, K— , HNO3-I- reddish. Phycobiont micareoid, cells<br />

4-7 /xm diam.<br />

Apo<strong>the</strong>cia <strong>of</strong>ten absent, at first adnate but <strong>of</strong>ten becoming constricted below, convex to<br />

subglobose, commonly tuberculate, immarginate or rarely very faintly marginate when young,<br />

matt or slightly glossy, dark blue-grey or black, 0- 15-0-4 mm diam, or to 0-7 mm diam when<br />

HNO3-I-<br />

tuberculate. Hymenium 45-60 /xm tall, hyaline or dilute green, but dark green (K— ,<br />

red) in upper part (epi<strong>the</strong>cium). Asci clavate, 40-55x14-16 /xm. Spores oblong-ellipsoid,<br />

oblong-fusiform or clavate-fusiform, <strong>of</strong>ten curved, (l-)3-septate, 14-26(-29)x4-5(-5-5) /xm.<br />

Paraphyses numerous, branched and anastomosing, (0-7-)l-l-5 /xm wide; apices <strong>of</strong>ten more

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