PERSOONIA. from the Netherlands. crassis vel cristalliferis. Ab C. citrinus differt sporis. Utrecht, Nijenrode, Breukelen, 20.X.2001, G.

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Fig. PERSOONIA Volume 18, Part 2,231-237 (2003) Crepidotus cristatus, anewyellowspecie from the Netherlands Beatrice Senn-Irlet ' & Gert Immerzeel 2 Crepidotus cristatus is described as a new species close to C. citrinus. Distinctive features are the yellow colour of the fruit-bodies,(sub-)globose small cheilocystidia with finger-like outgrowths, thick-walled epicuticular hyphae nearthe point spores, of attachment and small crystals on the cystidia and on the pileipellis. A collection of Crepidotus from an estate in the Netherlands proved to represent an undescribed species with noteworthy characters such as crystals on the cheilocystidia, typical of species known from the paleotropics and Australia/NewZealand. Crepidotus cristatus Senn-Irlet & Immerzeel, spec. nov. 1-3 Pileo 2-10 mm lato, reniformi vel conchiforme, citrino-luteo perstrigoso. Lamellis excentrice concurrentibus,pallide luteis dein brunneis. Stipite iuventute praesenti, cylindrico, sublaterali. Sporis 5.0-6.5 x 4.5-6.5 pm, globosis vel subglobosis, verrucosis,brunneis. Basidiaclavata, 20-30 x 6-8 /im, 4-sporigera. Cheilocystidiis 20-30 x 6-15 fim, utriformis, cristalliferis,hyalinis, appendicibus valde diverticulatis praeditis. Cuticula valde tomentosa ex hyphis laxe intricatis fibuligeris, parte tunicis 0.2-0.5 jun crassis vel cristalliferis. Ab C. citrinus differt sporis minoribus. Ad corticem arborum, Hollandia. Holotypus: The Netherlands, prov. Utrecht, Nijenrode, Breukelen, 20.X.2001, G. Immerzeel (12001-302(L; Paratypus ZT)). Pileus 2-10 mm, irregularly rounded flabelliform, reniform, rarely semicircular, mostly ungulate when young, later plano-convex or with a low umbo at point of attachment, irregularly waved when old, with distinctly incurved margin, mat, feltedtomentose,pale sulphur to lemon yellow, butter yellow (Methuen 3A4-3A5,4A4-A5), in dried specimen buffto ochraceous, not hygrophanous, sessile, at point of attachment tomentose-villose. LamellaeL = 6-14,1 = 1-3, rather narrow, moderately crowded, subventricose, narrowly adnexed, young pale yellowish, later cinnamon-buff to cinnamon; edge white, distinctly fimbriate. Stipe visible only in very young, undeveloped fruit-bodies, curved, tomentose. Flesh thin, white. Taste slightly farinaceous, smell fungus-like. Spores 5.0-6.5 x 4.5-6.5 pm, Q 1-1.25, = mean volume92 3 /<m, globose, sometimes subglobose, punctate-warty, verruculose (type 1 sensu Senn-Irlet, 1995); walls moderately coloured. Basidia 20-30 x 6-8 /<m, four-spored, clamped. Cheilocystidia 20-30 x 6-15 pm (including outgrowths), clavate, narrowly utriform, with short finger-like, up to 3 pm wide protuberances, which may be branched, angled or flexuous, antlerlike, in upper part covered with scattered small crystals. Trama of lamellae subregular. 1) WSL, Swiss Federal Research Station, CH-8903 Birmensdorf,Switzerland. 2) Straatweg 23, NL-3621 BB Breukelen, The Netherlands.

Vol. 232 PERSOONIA - 18, Part 2, 2003 Fig. 1. Crepidotus cristatus. Line-drawings from pileipellis (a, near cap margin) and in the centre (b), basidia, spores, and cheilocystidia. Scale bars = 10 μm.

Senn-Irlet & Immerzeel: Crepidotus crislalus spec. Nov. 233 Fig. 2. Crepidotus cristatus. Fresh carpophores from collection GI1999-101 (above) and from collection GI2001-302 (below). Pileipellis a transition between a trichodermand a cutis with mostly straight, more rarely flexuous, filiform, 2-3 wide /<m hyphae; in lower part scattered fragments covered with small crystals and slightly thick-walled hyphae not rare; terminalcells undifferentiated, especially at pileus margin often in the shape of cheilocystidia with outgrowths and covered with small cuboidcrystals; strigose hairs at point ofattachment composed of straight, slightly thick-walled hyphae. Pileitrama regular, hyaline. Pigment yellowish, rather indistinct, intracellularand faintly membranaceous in pileipellis, dissolving in ammonia. Clamp-connections abundantin all tissues.

On Senn-Irlet & Immerzeel: Crepidotus cristatus spec, nov 235 Pileipellis a transition between a trichodermand a cutis with mostly straight, more rarely flexuous, filiform, 2-3 pm wide hyphae; in lower part scattered fragments covered with small crystals and slightly thick-walled hyphae not rare; terminalcells undifferentiated, especially at pileus margin often in the shape of cheilocystidia with outgrowths and covered with small cuboid crystals; strigose hairs at point ofattachment composed of straight, slightly thick-walled hyphae. Pileitrama regular, hyaline. Pigment yellowish, rather indistinct, intracellularand faintly membranaceous in pileipellis, dissolving in ammonia. Clamp-connections abundant inall tissues. Habitat various fallen corticated branches of up to 15 cm diameterof Acer pseudoplatanus, Buxus. Together with Nectria spec. Collections examined. THE NETHERLANDS: prov. Utrecht, Nijenrode, Breukelen, 8.XI.1999, G. Immerzeel GI1999-101 (L); idem 20.X.2001, G. ImmerzeelGI2001-302 (L, holotype). Fig. 3. Crepidotus cristatus. a-c. Spores, crystals on collapsed cheilocystidia; d. arrowhead. Scale bars = 10 μm.

Vol. 236 PERSOONIA - 18, Part 2, 2003 DISCUSSION This species is characterised by the combinationofa small cheilo- yellow fruit-body, cystidia with finger-like outgrowths and cuboid crystals. Among the hitherto known European species with cystidia of such shape and size are C. carpaticus and C. roseoornatus. While the latter is a reddish-coloured species, C. carpaticus with cream-bufffruit-bodies may also display yellowish tints. However, its cheilocystidia lack crystals. In addition the SEM pictures show a slightly different type of spore ornamentation: isolated hemispherical warts in the new species (Fig. 3 a-c), irregular, confluentwarts attimes decoratedwith small outgrowths in C. carpaticus (Senn-Irlet, 1995). In the North American mycoflora (Hesler & Smith, 1965) Crepidotus contortus Hesler & A. H. Sm. seems to come close with pale olive buffcolours, globose spores and small, exceptionally strongly contorted cheilocystidia. The cystidia in our species cannot be described as contorted, they form a dense band not easy to detach for a microscopic analysis as the outgrowths sometimes intermingle. In addition the presence of crystals is not reported for C. contort us. Crystal bearing cheilocystidia are known from several species in the Crepidotus episphaeria-complex from the Southern hemisphere (Reid, 1975;Horak, 1977). However, noneof these species have the same shape ofcystidia. Table I. Distinctive sizes (in μm) and features of six collections of the complex around Crepidotus citrinus. species collection mean mean cheilo- shape of presence number of spore spore cystidia cheilo- crystals spores length in widthin size in //m cystidia per pirn /*m basidium (N = 20) (N =20) sulphurinus CBM-FB 7.7 7.5 30-46x utriform scattered on 2 11123 6-10 cheilocystidia sulphurinus CBM- 8.0 7.5 14-42 x utriform scattered on 2 2281 8-11 cheilocystidia citrinus PR-3434 7.7 7.3 19-43 x utriform scattered on 2 7-10 & antlerlike cheilocystidia and pileipellis citrinus RE-68 7.8 7.4 25-45 x antlerlike abundant on 2-4 6-10 cheilocystidia cristatus GI 5.7 5.4 22-35 x antlerlike scattered on 4 1999-101 6-10 cheilocystidia cristatus GI 6.0 5.5 18-28 x antlerlike abundant on 4 2001-302 7-14 cheilocystidia and scattered on pileipellis

Senn-Irlet & Immerzeel: Crepidotus cristatus spec. Nov. 237 Localities. CBM-FB-11123: Japan,Chibapref., Higashi-yamashina-cho, Midori-kuz, 14.VI.1994,leg. Ostuta & Isoda; CBM-2281: Japan, Chiba pref., Kiyosumi-yama, Amatsu-kominato-cho,Awa-gun, 300-350 m, broad-leaved forest mixed with Quercus acuta,.and Castanopsis cuspidata, 8.VII. 1989, leg. T. Fukiharu; PR-3434: Puerto Rico, Luquillo Mountains, Mun. de Rio Grande, Caimitillo Trail, 700 m, 2.X.1996, leg. S.A. Cantrell; RE-68: La Reunion, Foret de Belouve, 13.III.1996, leg. A. Hausknecht & G. Wolfel. Crepidotus citrinus Petch, a species with a mainly (sub-)tropical distribution, has larger, intensely coloured golden-brown spores and two-spored basidia (Singer, 1973). There is a difficulty in the unequivocal interpretation ofthis species, as hitherto published type studies do not mention the shape ofthe cheilocystidia (Pilat, 1951) nor the crystals and the thick-walled hyphae of at least parts of the pileipellis (Pegler, 1986). These structures seem to be destroyed in the type collection. Singer (1973) illustrates quite bizarre cheilocystidia shapes from a collection from Argentina which have the same antler-like pattern as our species. Own observations on several collections fromall over the world with distinct yellow fruit-bodies have convinced us that ic. citrinus should be interpreted as a species with antler-like cheilocystidia, scattered crystals at least in the cheilocystidia and often in addition in the pileipellis, and thick-walled epicuticular hyphae especially near the point ofattachment. In contrast to the original description of C. citrinus, Japanese authors offer a more exhaustive description of another similar species, C. sulphurinus Imazeki & Toki. Already the original description mentionsrare incrustations of the cheilocystidia. The study of Japanese collections of " C. sulphurinus showed utriform cheilocystidia with scattered small crystals and the presence ofthick-walled hyphae in the epicutis. Yet, the basidia are all two-spored, the spores larger (see Table I) and in one collection coarse yellow agglutinated crystals were present in the trama. In contrast to Singer (1973) who interpreted C. sulphurinus as a synonym of C. citrinus we treat these two as distinct species, with the main differencefound in the shape ofthe cystidia. ACKNOWLEDGEMENTS We thank Marco Herwegh from the Institute of Geological Sciences (Bern)for the SEM pictures and T. Fukiharu from the Natural History Museum and Institute Chiba (Japan). A. Hausknecht (Vienna, Austria) and Jean Lodge from the Center of Forest Mycology Research (Puerto Rico) for the loan of various Crepidotus collections. REFERENCES Hesler, L. R. & A.H. Smith. 1965. North American species of Crepidotus. Hafner, New York. Horak, E. 1977. Crepidotus episphaeria and related species from the Southern Hemisphere. Ber. Schweiz. Bot. Gesellschaft 87: 227-235. Kornerup, A. & J.H. Wanscher. 1978. Methuen handbook of colours. 3rd ed. London. Pegler, D. 1986. Agaric Flora of Sri Lanka. Kew Bull. Add. Series XII. Pilat,A. 1951. Revision of the types of some extra-european species ofthe genus Crepidotus. Trans. Brit. My col. Soc. 33: 215-249. Reid, D. 1975. Type studies of larger basidiomycetes Herb. 7: 1-255. described from Southern Africa. Contr. Bolus Senn-Irlet, B. 1995. The genus Crepidotus (Fr.) Staude in Europe. Persoonia 16: 1-80.