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Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975

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Basidiodendron cremeum (McNabb) K. Wells & Raitv., Mycologia 67 909 (1975)
Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975

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Indigenous
Present
New Zealand
Political Region

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(McNabb) K. Wells & Raitv.
McNabb
K. Wells & Raitv.
1975
909
ICN
NZ holotype
species
Basidiodendron cremeum

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On dead Melicytus ramiflorus, Auckland, Thames, Kauaeranga Valley, 26.VIII.l954, J. M. Dingley (HOLOTYPE, PDD 25006); Lake Rotoehu, 10.IX.1954, G. H. Cunningham, PDD 25007.
Fructifications waxy to arid-waxy, resupinate, thin, effused, originating as discrete patches, coalescing to form irregular areas to 17 cm in longest dimension, pruinose to farinaceous, pallid greyish-cream when fresh, changing little on drying; margins concolorous, adnate. In section 100-300 µm thick, consisting of basal layer and hymenium, occasionally two or more growth layers present. Basal layer thin, composed of indistinct, agglutinated, hyaline hyphae lying parallel with substratum, clamp connections present. Hymenium composed of dikaryophyses, gloeocystidia and basidia; dikaryophyses finely and irregularly branched apically, indistinct; gloeocystidia abundant, cylindrical to subclavate, often flexuous, arising from basal hyphae, hyaline at first, contents becoming yellow to brownish-yellow, granular, 42-78 x 5.2-9.7 µm; probasidia at first clavate, later obovate to pyriform, often distinctly stalked, proliferating through or near obscure basal clamp connections, 15.5-25 x 9-13 µm becoming longitudinally cruciate-septate; sterigmata subulate, to 25 µm long. Basidiospores broadly cylindrical, curved-cylindrical, or ovate and flattened on one side, hyaline, apiculate, 12.4-16.8-(19.6) x 5.3-6.6 µm. Germination by repetition or by stout germ tubes
Dead angiosperm wood.
Fructificationes ceraceae ad aride ceraceas, resupinatae, tenues, pruinosae ad farinaceas, pallide griseo-cremeae; ordo basalis tenuis, factus ex hyphis indistinctis, nodosis. Dikaryophyses subtiliter et irregulariter ramosae ad apicem; gloeocystidia cylindrica ad subclavata, interiora brunneo-lutea, granulosa, 42-78 x 5.2-9.7 µm; probasidia obovata ad pyriformia, saepe stipulata, 15.5-25 x 9-13 µm, per longitudinem cruciata-septata; sterigmata subulata, ad 25 µm longa, Basidiosporae late cylindricae, curvo-cylindricae vel ovatae, 12.4-16.8-(19.6) x 5.3-6.6 µm Germinantes per repetitionem, vel tubulos.
Habitat in mortuo Melicyto ramiftoro.
Sebacina cremea is characterised by the cream, waxy to arid-waxy fructifications, obovate to pyriform, often stalked basidia with subulate sterigmata, and large cylindrical to curved-cylindrical spores.
Typus Auckland Province, Thames, Kauaeranga Valley, 26.VIII.l954, J. M. Dingley, PDD 25006.

Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975

Specimen examined.-R.S.F.S.R., Amurskaya Oblast', Mogot (Stanovoy Mts. ), on Salix sp., 29-VII-1961, E. Parmasto, TAA 7148. The holotype of Sebacina cremea McNabb (i.e., New Zealand: Auckland Prov., Thames, on Melicyus rami floras Forst., 26-IX-1954, J.M. Dingley, PDD 25006) was also studied.
Basidiocarps arid waxy to firm waxy gelatinous, effused, hyaline to pallid gray; upon drying forming a thin, grayish-white, porous-reticulate layer or a light to dark buff, vernicose crust, surface pruinose, sometimes cracking; margins adnate, usually lighter and fibrillose to porous-reticulate; in section 65-300 µm in thickness, consisting of a basal layer of prostrate hyphae giving rise to an ascending layer of fertile hyphae, gloeocystidia, and a few dikaryophyses, subhymenial hyphae thin walled with clamp connections, indistinct, becoming agglutinate, 1.5-3 µm in diam ; 2 or more growth strata sometimes formed; gloeocystidia abundant, subcylindrical, becoming yellow-granular and flexuous, often with hyaline, staining apex, sometimes with knoblike base laterally attached, 19-75 x 4-9.5 µm; dikaryophyses sparse, simple to sparingly branched, 1-2 µm in diam; fertile hyphae forming basidia in dense lateral cluster or in close acropetal series, in thicker specimens surrounded by a loose involucre like sheath of collapsed basidia, sometimes branching, 2-4 µm in diam; hypobasidia elongate-elliptical, ovate, obovate, to clavate, more rarely pyriform, usually with 4 hypobasidial segments, with basal clamp connection, 14-22.5 x 9.5-13 µm; epibasidia tubular, somewhat attenuate, up to 21 µm in length, 2-3.5 µm in diam at the base; basidiospores allantoid, guttulate, (13-)14-19 x 4.5-7 µm, capable of germination by repetition.
Known from New Zealand.
Known only on decaying wood of Salix sp. and Melicytus ramiflorus.
Illustration.-McNabb, R. F. R. 1969. New Zealand J. Bot. 7: 251. Fig. 2, a-d.

Basidiodendron cremeum is clearly distinguished by the large allantoid basidiospores, the large basidia that are often obovate to clavate, or even pyriform, at maturity, and the well developed, tubular epibasidia. Basidia not forming distinct epibasidia are rare.

The features of the hymenium of the Russian collection are identical with those of the holotype; however, the two specimens differ in internal structure and in macroscopic aspect. Thus, we are somewhat reluctant in assigning the Russian collection to B. cremeum.

In TAA 7148 there is a relatively thick basal layer of agglutinate hyphae containing flexuous gloeocystidia. On this layer is a thin, prostrate layer giving rise to an ascending layer of fertile hyphae and gloeocystidia. Evidently the thicker basal layer represents the earlier development of the basidiocarp that has collapsed due to adverse environmental conditions. Portions of the type are composed of five growth strata, whereas near the margins of the portion examined often only a single growth stratum is present. These differences in structure can be attributed, we believe, to divergent environmental conditions during growth. Such variations have been observed in other more common species, such as B. cinereum and B. eyrei.

The type collection is continuous and grayish buff when dry, but portions near the margins are porous-reticulate. The Russian collection when dry is porous-reticulate to fibrillose and grayish white. These differences are possibly correlated with the fact that the type is a much thicker specimen (100-300 µm) than the Russian collection (65-190 µm). The Russian collection has only a single, organized growth stratum, and the hymenium is interrupted.

We believe these differences in internal structure and macroscopic aspect are probably due to different substrata, different environmental conditions during basidiocarp development, or possibly different ages at the time of collection. Since such variations have been observed frequently in other species of Basidiodendron, it would not be advisable at this time to base a new species on the Russian collection.

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Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975
Basidiodendron cremeum (McNabb) K. Wells & Raitv. (1975)
Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975
Basidiodendron cremeum (McNabb) K. Wells & Raitv. (1975)
Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975
Basidiodendron cremeum (McNabb) K. Wells & Raitv. (1975)

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Basidiodendron cremeum (McNabb) K. Wells & Raitv. 1975
[Not available]

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1cb17f2a-36b9-11d5-9548-00d0592d548c
scientific name
Names_Fungi
22 December 1999
27 June 2003
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