Haploporus pirongia (G. Cunn.) Meng Zhou, Y.C.Dai&T.W. May
publication ID |
https://dx.doi.org/10.3897/mycokeys.54.34362 |
persistent identifier |
https://treatment.plazi.org/id/66998AF0-F2B0-9306-3363-EF0B87369C2B |
treatment provided by |
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scientific name |
Haploporus pirongia (G. Cunn.) Meng Zhou, Y.C.Dai&T.W. May |
status |
comb. nov. |
Haploporus pirongia (G. Cunn.) Meng Zhou, Y.C.Dai&T.W. May comb. nov. Figs 10, 11
Poria pirongia G. Cunn., Bull. N.Z. Dept. Sci. Industr. Res., Pl. Dis. Div. 72: 39 (1947) (Basionym)
Etymology.
the epithet pirongia, derived from the type locality, Mount Pirongia, is a noun in apposition, and therefore remains spelt the same when transferred from Poria to Haploporus , despite the latter genus being masculine in gender.
Fruitbody.
Basidiocarps annual, resupinate, difficult to separate from the substrate, soft corky when fresh, corky upon drying, odor- or tasteless when fresh, up to 8 cm long, 2 cm wide and 1.7 mm thick at center. Pore surface white to cream when fresh, pale brownish when bruised, pinkish buff to clay-buff upon drying; sterile margin very narrow to almost lacking; pores round to angular, 3-4 per mm; dissepiments thick, entire. Subiculum cream, corky, thin, about 0.3 mm thick. Tubes light buff, corky, about 1.4 mm long.
Hyphal structure.
Hyphal system trimitic: generative hyphae bearing clamp connections, hyaline, thin-walled, frequently branched; skeletal hyphae dominant, thick-walled to subsolid, hyaline to slightly yellowish, frequently branched; binding hyphae abundant, slightly thick-walled, IKI–, CB+, tissues unchanging in KOH.
Subiculum.
Generative hyphae frequent, hyaline, thin-walled, frequently branched, 2.3-3.5 µm in diam; skeletal hyphae dominant, hyaline, distinctly thick- walled with a narrow lumen to subsolid, occasionally branched, interwoven, 2.5-4 µm in diam; binding hyphae abundant, slightly thick-walled,1-2 µm in diam.
Tubes.
Generative hyphae frequent, hyaline, thin-walled, frequently branched, 1.7-3.5 µm in diam; skeletal hyphae distinctly thick-walled with a narrow to wide lumen, frequently branched, interwoven, 2.5-4 µm in diam; binding hyphae slightly thick-walled,1-2.5 µm in diam. Cystidia absent; cystidioles present, fusiform, occasionally with an apical simple septum, sometimes with a few small guttules, 21-28 × 5-7 µm. Basidioles dominant, similar in shape to basidia, but slightly smaller, occasionally with a few large guttules; basidia pear-shaped to barrel-shaped with 4-sterigmata and a basal clamp connection, 21-35 × 8-11 µm. Hyphae at dissepiment usually thick-walled with simple septum. Dendrohyphidia absent. Some irregular-shaped crystals present among tube tramal structures.
Spores.
Basidiospores oblong-ellipsoid to cylindrical, hyaline, thick-walled, with tuberculate ornamentations, some with a guttule, IKI–, CB+, 11 –14(– 15) × (4.8 –)5.2– 7 µm, L = 12.35 µm, W = 6.11 µm, Q = 1.83-2.15 (n = 90/3).
Specimens examined.
AUSTRALIA. Victoria, Melbourne, Dandenong Ranges Botanical Garden, on dead branch of Rhododendron , 12 May 2018, Dai 18659, 18660 & 18661 (MEL, dupl. in BJFC); on dead branch of Eucalyptus , 12 May 2018, Dai 18662 (MEL, dupl. in BJFC). NEW ZEALAND. Omahu Bush, on Melicytus , 15 Feb 2010, Cooper (PDD 95714, dupl. in BJFC).
No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.
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