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Bulletin of the British Museum (Natural History)

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LICHEN GENUS MICAREA IN EUROPE 189<br />

when tuberculate. Hymenium 35-45 /xm tall, dilute olivaceous or dilute olive-brown, K+ violet:<br />

pigment confined to gel-matrix. Asci clavate, 30-40x9-5-12 jxm. Spores ± acicular or rodshaped,<br />

curved or ± straight, l-7(-ll)-septate, 14^35(-43)xl-8-2-5(-3) y,m. Paraphyses<br />

numerous, branched, sometimes anastomosing, 0-8-1 /xm wide, sometimes widening to 1-5 /am<br />

towards <strong>the</strong>ir apices; apical walls hyaline. Hypo<strong>the</strong>cium 60-100 jxm tall, hyaline, or dilute<br />

olivaceous and <strong>the</strong>n Kf+ violet; hyphae hyaline, 1-2 ^im wide, interwoven or some ± vertically<br />

orientated in <strong>the</strong> upper part; intermixed with short-celled ascogenous hyphae, c. 2-4 ^im wide.<br />

Excipulum indistinct, evident in sections as a narrow, reflexed, non-amyloid lateral border to<br />

<strong>the</strong> hymenium, hyaline or pale olivaceous (<strong>the</strong>n K+ violet), varying from paler to darker than<br />

<strong>the</strong> hymenium; hyphae hyahne, radiating branched and anastomosing, c. 1 /xm wide.<br />

Pycnidia frequent but inconspicuous, immersed within areolae, or emergent to sessile,<br />

whitish to grey-black; walls dull olivaceous (pigment <strong>of</strong>ten more intense around <strong>the</strong> ostioles),<br />

K+ violet. Pycnidia <strong>of</strong> two types: (a) 60-120 /am diam, immersed, or emergent with gaping<br />

ostioles; conidia {mesoconidia) ± cylindrical to fusiform, 4-5-6xl-2-l-5 /xm; (b) 30-40 /Ltm<br />

diam, immersed to sessile, but ostioles not gaping; conidia (microconidia) short-cylindrical,<br />

3-8-4-8x0-8-l/xm.<br />

Chemistry: Thallus C— , K— , PD— ; sections <strong>of</strong> thallus and apo<strong>the</strong>cia C- (but olivaceous parts<br />

C-l- violet due to pigment); t.l.c: no substances detected.<br />

Observations: Micarea syno<strong>the</strong>oides is characterized by its ± acicular or rod-shaped spores,<br />

K-l- violet hymenium, and olivaceous thallus which is j. gelaimous when wet. M. globulosella is<br />

very similar, but differs in having a thallus <strong>of</strong> whitish or grey, somewhat larger areolae<br />

containing gyrophoric acid. M. nitschkeana differs in <strong>the</strong> same ways, and in addition has shorter<br />

(rarely over 17 jxm) spores and longer microconidia. M. globulosella and M. syno<strong>the</strong>oides have<br />

been confused with Bacidia beckhausii (see p. 196) which has similar spores, pigmentation and<br />

paraphyses, but can be distinguished by its large-celled (c. 8-14 fxm diam) phycobiont,<br />

excipulum <strong>of</strong> coherent (in K) hyphae, smaller conidia (one type only, c. 2-8-3-5X 1-1-4 /xm),<br />

<strong>of</strong>ten pruinose apo<strong>the</strong>cia, and usual occurrence on less acidic bark (especially <strong>of</strong> Acer, Fraxinus,<br />

Populus, and Ulmus), although it does occasionally occur on Quercus trunks and more rarely on<br />

lignum.<br />

Of <strong>the</strong> four Japanese specimens, two are on bark and two (type material) are on lignum. They<br />

all have ra<strong>the</strong>r siiprt spores (14-26 /xm), but appear to agree in most o<strong>the</strong>r respects with<br />

collections from Britain and <strong>the</strong> Atlantic islands. Unfortunately I was unable to find mesoconi-<br />

dia in <strong>the</strong> Japanese specimens. For <strong>the</strong> time being, I consider <strong>the</strong> Japanese and Atlantic<br />

populations as conspecific, especially as <strong>the</strong> <strong>British</strong> collections exhibit considerable variation in<br />

spore septation and length. Fur<strong>the</strong>r collections from Japan are required to finally establish <strong>the</strong><br />

relationship between <strong>the</strong> two populations.<br />

Habitat and distribution: M. syno<strong>the</strong>oides is an oceanic species mostly found in wooded valleys<br />

on bark or over bryophytes, on <strong>the</strong> trunks <strong>of</strong>, for example, Alnus, Betula, Quercus, Larix,<br />

Pinus, and Pseudotsuga, in communities in, or related to, <strong>the</strong> Parmelion laevigatae alliance.<br />

<strong>British</strong> collections include <strong>the</strong> following associated lichens: Bryoria fuscescens, Chrysothrix<br />

candelaris, Cladonia coniocraea, C. squamosa, Haematomma elatinum, Hypogymnia physodes,<br />

Lecanactis abietina, Lecidea icmalea, Micarea alabastrites, M. cinerea, M. peliocarpa, M.<br />

stipitata, Mycoblastus sterilis, Ochrolechia androgyna, Parmelia saxatilis, Pertusaria amara,<br />

Platismatia glauca, Sphaerophorus globosus, Trapelia corticola in ed., and Usnea subftoridana.<br />

The single <strong>British</strong> collection on lignum {Coppins 2299) was on a rotting trunk <strong>of</strong> Pinus. In <strong>the</strong><br />

Canary Islands it occurs on Erica arborea in a photophobus and hydrophilic community<br />

composed <strong>of</strong> crustose lichens with Atlantic distributions (Topham & Walker, loc. cit.). In <strong>the</strong><br />

Azores it occurs in a more or less identical community on Cryptomeria.<br />

Apart from <strong>the</strong> type locality in Japan, it is known only from western Britain, <strong>the</strong> Azores, and<br />

<strong>the</strong> Canary Islands (Tenerife). It should be sought for in suitable habitats in o<strong>the</strong>r oceanic parts<br />

<strong>of</strong> Europe (e.g. south-west Norway, Bretagne, <strong>the</strong> Pyrenees, and Portugal).

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