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Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988

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Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden, Mycotaxon 31 5 (1988)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Buchanan, P.K.; Ryvarden, L. 2000: An annotated checklist of polypore and polypore-like fungi recorded from New Zealand. New Zealand Journal of Botany 38(2): 265-323.

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Indigenous, non-endemic
Present
New Zealand
Political Region
Anon

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(Berk.) P.K. Buchanan & Ryvarden
Berk.
P.K. Buchanan & Ryvarden
Buchanan, P.K.; Ryvarden, L. 1988: Type studies in the Polyporaceae - 18. Species described by G.H. Cunningham. Mycotaxon 31(1): 1-38.
1988
5
ICN
Polyporus tasmanicus Berk. 1859 [1860]
species
Australoporus tasmanicus

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Fungi
Basidiomycota
Agaricomycetes
Polyporales
Polyporaceae
Australoporus
tasmanicus

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Associations View full associations record
has host
Dysoxylum spectabile (G.Forst.) Hook.f.
Cunningham, G.H. (1948)
has host
Dysoxylum spectabile (G.Forst.) Hook.f.
Cunningham, G.H. (1949)
has host
Beilschmiedia tarairi (A.Cunn.) Kirk
Dingley, J.M. (1969)
has host
Beilschmiedia tarairi (A.Cunn.) Kirk
Gadgil, P.D. (in association with Dick, M.A.; Hood, I.A.; Pennycook, S.R.) (2005)
has host
Nothofagus menziesii (Hook.f.) Oerst.
Gilmour, J.W. (1965)
has host
Beilschmiedia tarairi (A.Cunn.) Kirk
Gilmour, J.W. (1966)
has substrate
Nothofagus fusca (Hook.f.) Oerst.
Hood, I. A.; Beets, P. N. et al. (2008)
has substrate
Nothofagus
Hood, Ian A.; McDougal, Rebecca L. et al. (2019)
has host
Nothofagus solandri (Hook.f.) Oerst. var. solandri
Lloyd, G.C. (1915)
has host
Nothofagus
McKenzie, E.H.C.; Buchanan, P.K.; Johnston, P.R. (2000)
has host
Beilschmiedia tarairi (A.Cunn.) Kirk
Cunningham, G.H. (1965)
has host
Nothofagus menziesii (Hook.f.) Oerst.
Cunningham, G.H. (1965)
has host
Dysoxylum spectabile (G.Forst.) Hook.f.
Cunningham, G.H. (1965)
has host
Beilschmiedia tarairi (A.Cunn.) Kirk
Pennycook, S.R. (1989)
isolated from
Dacrycarpus dacrydioides (A.Rich.) de Laub.
ICMP (1 records from [Not available].) Link to an external page
isolated from
Nothofagus menziesii (Hook.f.) Oerst.
ICMP (1 records from [Not available].) Link to an external page
isolated from
Nothofagus moorei (F.Muell.) Krasser 1896
ICMP (1 records from [Not available].) Link to an external page
isolated from
Nothofagus solandri var. cliffortioides (Hook.f.) Poole
ICMP (1 records from [Not available].) Link to an external page
has host
Agathis australis (D.Don) Lindl.
PDD (1 records from [Not available].) Link to an external page
has host
Beilschmiedia tarairi (A.Cunn.) Kirk
PDD (4 records from [Not available].) Link to an external page
has host
Beilschmiedia tawa (A.Cunn.) Kirk
PDD (15 records from [Not available].) Link to an external page
has host
Dysoxylum spectabile (G.Forst.) Hook.f.
PDD (2 records from [Not available].) Link to an external page
has host
Fuscospora cliffortioides
PDD (1 records from [Not available].) Link to an external page
has host
Ixerba brexioides A.Cunn.
PDD (1 records from [Not available].) Link to an external page
has host
Lophozonia menziesii (Hook.f.) Heenan & Smissen 2013
PDD (1 records from [Not available].) Link to an external page
has host
Nothofagus
PDD (10 records from [Not available].) Link to an external page
has host
Nothofagus cliffortioides
PDD (1 records from [Not available].) Link to an external page
has host
Nothofagus cunninghamii
PDD (2 records from [Not available].) Link to an external page
has host
Nothofagus fusca (Hook.f.) Oerst.
PDD (11 records from [Not available].) Link to an external page
has host
Nothofagus menziesii (Hook.f.) Oerst.
PDD (18 records from [Not available].) Link to an external page
has host
Nothofagus moorei (F.Muell.) Krasser 1896
PDD (3 records from [Not available].) Link to an external page
has host
Nothofagus solandri (Hook.f.) Oerst.
PDD (2 records from [Not available].) Link to an external page
has host
Nothofagus solandri var. cliffortioides (Hook.f.) Poole
PDD (6 records from [Not available].) Link to an external page
has host
Weinmannia
PDD (1 records from [Not available].) Link to an external page
has host
Weinmannia racemosa L.f.
PDD (4 records from [Not available].) Link to an external page

Click to collapse Descriptions Info

Buchanan, P.K.; Ryvarden, L. 1988: Type studies in the Polyporaceae - 18. Species described by G.H. Cunningham. Mycotaxon 31(1): 1-38.

Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988

Cunningham (1965) transferred the species to Flaviporus Murr., while stating that apart from the presence of 'metuloids' the species could belong in Heterobasidion Bref. sensu Cunn. Comparison of the type specimens of Poria aroha, Polyporus tasmanicus Berk. (K), Fomes cuneatus Lloyd (K), and Polyporus suaderis Lloyd (K) show that all are conspecific, with P. tasmanicus being the oldest name.
Macroscopically, the species varies from resupinate to distinctly pileate. The perennial, narrowly concentrically sulcate and zonate, often ungulate pileus and the pale pink to orange pore surface, when fresh, are diagnostic characters.
In the descriptions of both H. tasmanicum and Flaviporus aroha, Cunningham (1965) mistakenly reported generative hyphae to be simple septate when, in fact, they have clamps. He also omitted to report that skeletal hyphae are strongly dextrinoid, becoming red-brown in Melzer's reagent. Skeletal hyphae often protrude into the hymenium, and at pore mouths the ends of skeletal hyphae are finely encrusted. The thick-walled metuloids described for F. aroha were found to be thin-walled, sometimes collapsed, apically encrusted cystidioles. They are more abundant in fertile specimens and may be scarce or absent in old specimens with a poorly preserved hymenium. Spores are elongate ellipsoid, smooth- and thin-walled, nonamyloid, nondextrinoid, and hyaline in the tubes. Those observed on the pileus surface however are light brown and often larger than those in the tubes. Average spore measurements are 8.5-13 x 3.5-6.5 µm.
The unusual combination of characters found in P. tasmanicus means that the species cannot be accommodated in any of the four genera to which Cunningham assigned it. Indeed, we have found no suitable genus for this species.
Dextrinoid skeletal hyphae are found in species of Perenniporia Murr., but this genus has distinctly truncate, thick-walled spores with a variable dextrinoid reaction and lacks encrusted skeletal hyphae. Navisporus Ryv. is a close relative, having dextrinoid skeletal hyphae and navicular to cylindrical spores of similar size to those in Polyporus tasmanicus. However, skeletal hyphae are smooth and no encrusted cystidioles are known in the two species so far described in the genus. Furthermore, the species are brown in colour and have a loose consistency, very different from the hard, light-coloured fruit-bodies of P. tasmanicus. Junghuhnia Corda is characterised by a dimitic hyphal system of a similar type to that found in P. tasmanicus. Cystidia are present, but are developed from the skeletal hyphae and are encrusted at the apex. Thin-walled, ventricose cystidia have not been observed in this genus and the skeletal hyphae are not dextrinoid.
Since this species cannot be accommodated in any known genus without changing the concepts of that genus, we propose a new genus for P. tasmanicus [Australoporus].
Cunningham, G.H. 1947: New Zealand Polyporaceae. 1. The genus Poria. New Zealand Department of Scientific and Industrial Research, Plant Diseases Division, Bulletin. 72.

Poria aroha G. Cunn. 1947

Beilschmiedia tawa (A.Cunn.) Hook.f. & Benth., on bark of dead fallen trunk. Auckland. Mt. Te Aroha, 1,500 feet, Nov. 1946, G.H.C. type collection.
Hymenophore effused, to 16 x 5 cm., 2-4 mm. thick, firm with numerous outlying islands; surface cream or isabelline, or occasionally drying some shade of brown, even, or undulating and nodose ; margin irregular, rounded, waved, finely tomentose, byssoid, sterile for a width of 2-3 mm., lifting. Pores not in strata, round or angular, often oblique, in section pallid isabelline, to 4 mm. deep, 100-150 µ diameter, or 4-5 to mm.; dissepiments 50-150 µ, occasionally to 500 µ thick, equal, of woven partly parallel hyphae, apices tapering, firmly woven, a few apical hyphae with rounded apices and crystal coated. Context 1-2 mm. thick, floccose, pallid isabelline, closely woven, not gelatinized but with coloured gelatinous matter scattered between hyphae; skeletal hyphae to 4 µ thick, lumen 1-2 µ, staining less deeply in old hyphae which are more thickened in walls, aseptate, sparsely branched, somewhat irregularly waved near ends; generative hyphae to 2 µ thick, delicate walled, tinted by stains, somewhat sparingly branched and septate, readily collapsing, clamp connections present but scanty. Cystidia present in the hymenium, hyaline or tinted yellow, clavate, to 25 x 10 µ, walls about 3 µ thick, capped with crystals. Basidial type clavate, basidia clavate, scanty, to 16 x 1 µ, soon collapsing. Spores elliptical, 9-12 x 4-6 µ, hyaline, smooth, soon collapsing.
New Zealand.

Hymenophorum ad 16 x 5 cm., 2-4 mm. crassum, firmum, coriaceum, cremeum vel isabellinum. Pori rotundati, saepe obliqui, 3-4 mm. profundi, 100-150 µ diam.; dissepimenta 50-150 µ crassa. Contextus pallide isabellinus, 1-2 mm. crassus, textilis. Hypharum systema dimiticum. Hyphae skeletales sparse ramificatae, aseptatae, 3-4 µ crassae, lumine 1-2 µ; hyphae generatoriae ad 2 µ crassae, sparse ramificatae, septatae, fibulatae. Cystidia clavata, ad 25 x 10 µ, crystallis pilleata. Typus basidialis clavatus. Sporae ellipticae, 9-12 x 4-6 µ, leves, hyalina.

Hab.: Beilschmeidia tawa (A.Cunn). Hook.f. & Benth. Auckland, Mt. Te Aroha, 500 m., specimen typicum.

When fresh plants are white or cream, though a few may be coloured isabelline. Spores are present only in young plants, since basidia and spores early collapse, leaving only remnants attached to walls of dissepiments. Specimens possess a pleasant smell when freshly gathered, as of ripe peaches; this soon disappears when plants are dried. The large smooth spores separate the species from all save P. leucoplaca. From this it differs in the presence of capitate cystidia; thicker differently coloured hymenophore and scantily branched skeletal hyphae.
Cunningham, G.H. 1948: New Zealand Polyporaceae. 5. The genus Fomitopsis. New Zealand Department of Scientific and Industrial Research, Plant Diseases Division, Bulletin. 76.

Fomitopsis cuneata (Lloyd) G. Cunn. 1948

Dysoxylum spectabile (Forst.f.) Hook.f.
Auckland. Little Barrier Island, Nov. 1947, Joan Dingley.
Nothofagus menziesii (Hook.f.) Oerst.
Wellington. Day’s Bay, Aug. 1946, G.B.Rawlings.
Southland. Near Otautau, Nov. 1948, G.B.Rawlings; Woodlaw State Forest, Jan. 1947, G.B.Rawlings.
Weinmannia racemosa L.f.
Southland. Woodlaw, Nov. 1946, G.B.Rawlings.
Unknown Hosts
Auckland. Waipoua Kauri Forest, 1940, G.B.Rawlings.
Wellington. Mt. Kapakapanui, Tararua Ranges, Nov. 1946, A.P.Druce.

Hymenophore perennial, dimidiate, sometimes imbricate, firm and woody. Pileus effused-reflexed, applanate or ungulate, sometimes resupinate, 7-17 cm. x 2-5 cm. x 3-5 cm.; surface concentrically sulcate and ridged, fluted, nodose, bay brown, becoming umber, cuticle to 0.5 mm. thick, dark brown, shining, of compacted mainly woven hyphae cemented together; margin acute, entire, undulate, lighter in colour; hymenial surface at first ochraceous, drying bay brown, concave, sterile margin 2-3 mm. wide, finely tomentose, dissepiments not toothed. Context 2-5 mm. thick, pallid ochre or isabelline, of woven hyphae; skeletal hyphae to 4 μ thick, lumen 1 μ or almost obliterated, unbranched, aseptate, staining deeply; generative hyphee 2-3 μ thick, delicate walled, branched, septate, hyaline, not staining. Pores round, obscurely stratose, 2-4 mm. deep in each layer, pallid ochre in section, 100-200 μ diameter, or 5-6 per mm.; dissepiments 50-150 μ, most 50-75 μ, apices velutinate, enlarged, partly blocking pores. Basidial type clavate, basidia clavate, to 16 x 8 μ, soon collapsing. Spores elliptical, 6-8 x 4-5 μ, smooth, hyaline.
Australia; Tasmania; New Zealand.
Growing solitary, sometimes imbricate, upon bark or decorticated wood of dead standing trunks, associated with a white rot.

Resembling F. marginata in many micro-features the species differs in the smaller pores, differently shaped spores, thinner skeletal hyphae and different shape and surface of the pileus. Plants sometimes exude large drops from the surface of the hymenium. Sometimes these persist for so long that pore tissue grows between them, consequently when drops have disappeared the hymenium exhibits a pitted appearance.

In a former paper (1927, p. 210) I listed F. cuneata as a synonym of F. hemitephra, since Lloyd’s scanty description—based on New Zealand specimens at Kew collected from Nothofagus solandri by W.Colenso—suggested that it belonged to this species. His description of the spores was obviously based on those of some contaminating mould. Lloyd’s photograph of a Tasmanian specimen (1924, p. 1329), shows it to be valid and the same as the collections listed above. His Polyporus suaderis appears to be based on the same plant.

From F. hemitephra it may be separated by the different shape and surface of the pileus, larger spores, and absence of an orange zone beneath the cuticle.

Ruahine Ranges, New Zealand.
Cunningham, G.H. 1965: Polyporaceae of New Zealand. New Zealand Department of Scientific and Industrial Research, Bulletin. 164.

Flaviporus aroha (G. Cunn.) G. Cunn. 1965

FAGACEAE. Nothofagus fusca: Wellington, Tauherenikau Valley, Tararua Ranges, 300 m. Nelson, Murchison, 170 m; Staircase Creek, Reefton, 700 m. Westland, Orwell Creek, Ahaura. LAURACEAE. Beilschmiedia tarairi: Auckland, Waipoua Kauri Forest, 120 m. Beilschmiedia tawa: Auckland, Kauaeranga Valley, Thames, 70 m; Mt. Te Aroha, 500 m, type collection, P.D.D. herbarium, No. 5253; Whakarewarewa State Forest, 600 m; Te Whaiti, 500 m.
Hymenophore perennial, solitary, coriaceous, seldom pileate, commonly resupinate and loosely attached. Pilei merely upturned edges of one margin of broadly resupinate areas, with a radius of 8 mm; when resupinate effused to 16 x 5 cm, commonly 2-4 mm thick (in one specimen to 25 mm), with several outlying islands; pileus surface deep chestnut or umber, finely velutinate, concentrically sulcate; cortex to 200 µm thick, ferruginous, of mainly vertical hyphae compacted and partly cemented and with walls ferruginous; margin (of pilei) bluntly acute, concolorous, crenate (of resupinate specimens), irregular, thinning out, finely tomentose, lifting; hymenial surface white, drying cream or pallid tan, even, or undulating and nodose, each layer receding. Pores in 2-6 layers with context hyphae between, commonly in one or two layers, pallid isabelline, to 4 mm deep in each layer, round or angular, 4-5 per mm, 100-150 µm diameter; dissepiments 50-150 µm thick, occasionally to 500 µm, apices tapering, even, finely velutinate with erect hyphae, ends of which are crystal encrusted. Context 1-2 mm thick, straw or tan, closely intertwined and with coloured mucilage between hyphae; skeletal hyphae to 4 µm diameter, lumena 1-2 µm wide, aseptate, sparsely branched, irregularly waved towards ends, walls staining; generative hyphae to 2.5 µm diameter, walls 0.2 µm thick, somewhat sparingly branched and septate. Hymenial layer to 25 µm deep, a scanty palisade of basidia, paraphyses, paraphysate hyphae, and metuloids. Paraphysate hyphae merely projecting ends of skeletal hyphae, with thin walls encrusted with fine crystals. Metuloids clavate or fusiform, to 25 x 10 µm, walls hyaline or tinted, to 3 µm thick, capped with coarse crystals. Basidia clavate, 12-16 x 3.5-4 µm, bearing 4 spores; sterigmata erect, to 5 µm long. Paraphyses subclavate, 8-12 x 3-3.5 µm. Spores elliptical, apiculate, 9-12 x 4.5-6 µm, walls smooth, hyaline, 0.1 µm thick, soon collapsing.
New Zealand.
Bark or decorticated wood of dead fallen trunks, associated with a white rot.
Most collections are resupinate with one or several receding layers. In two, pilei are present, appearing as scantily developed margins of upper edges of plants growing vertically upon fallen logs. A well developed cortex is present in them, indicating that they are genuine pilei. When fresh the hymenial surface is white, although in some specimens it may be isabelline, changing in drying to some shade of brown. One collection taken from the under side of a fallen log was 1.5 m long, 2.5 cm thick, and composed of six receding layers. When fresh, plants possess a fragrant odour as of ripe peaches. Metuloids are scanty, but readily seen as they project to 10 µm, possess thick and refractive, usually tinted walls, and are capped with coarse crystals. Paraphysate hyphae are also present, both in the hymenial layer and at apices of dissepiments. The species is somewhat difficult to place. Other than for the presence of metuloids, it is a typical Heterobasidion; the presence of metuloids places it under Flaviporus with which it agrees in several features.
LOCALITY: Mt. Te Aroha, Auckland.
Cunningham, G.H. 1965: Polyporaceae of New Zealand. New Zealand Department of Scientific and Industrial Research, Bulletin. 164.

Heterobasidion tasmanicum (Berk.) G. Cunn. 1965

CUNONIACEAE. Weinmannia racemosa: Auckland, Te Whaiti, 300 m. Otago, Doubtful Sound, 130 m; Woodlaw State Forest. ESCALLONIACEAE. Ixerba brexioides: Auckland, Mamaku Forest, 600 m. FAGACEAE: Nothofagus cliffortioides: Nelson, Lake Rotoiti, 700 m. Nothofagus fusca: Nelson, Marble Mountain, Maruia, 900 m; Westland, Orwell Creek, Ahaura. Nothofagus menziesii: Auckland, Mamaku Forest, 600 m. Wellington, Days Bay, 120 m. Nelson, Kakapo River, 300 m; Little Wanganui River, 270 m. Otago, Black Gully, Blue Mountains; Hollyford Valley, 140 m; Milford Sound, 200 m; Lake Te Anau, 120 m; Woodlaw State Forest; Alton Valley, Tuatapere, 120 m. LAURACEAE. Beilschmiedia tarairi: Auckland, Waipoua Kauri Forest, 130 m; Kaukapakapa. Beilschmiedia tawa: Auckland, Moumoukai Valley, Hunua Ranges, 300 m; Kauaeranga Valley, Thames, 70 m; Lake Rotoehu, 450 m; Earthquake Flat, Rotorua, 600 m. MELIACEAE. Dysoxylum spectabile: Auckland, Little Barrier Island. UNKNOWN HOSTS. Auckland, Waikaretu, 140 m; Waipoua Kauria Forest; Te Whaiti; Whakamarama. Wellington, Mt. Kapakapanui. Victoria, Cumberland Valley. Tasmania, National Park; Between Great Lake and Deloraine; National Park.

IN KEW HERBARIUM: Collections are the type ex "Tasmania, Archer", "Tasmania, L. Rodway" type of Polyporus suaderis Lloyd, and "N.Z. Colenso, b 369" type of Fomes cuneatus Lloyd.

Comb. nov.

Hymenophore perennial, solitary or imbricate, firm and woody, attached by a broad lateral base. Pilei usually effused-reflexed, sometimes ungulate or applanate, occasionally resupinate, 7-17 cm, 2-5 cm radius, 3-5 cm thick; pileus surface bay, becoming umber, concentrically sulcate and ridged, radiately fluted and/or rugulose, nodose; cortex to 0.5 mm thick, dark brown, shining, of compactly intertwined cemented hyphae; margin acute, entire, undulate, lighter in colour; hymenial surface ochre drying bay, with a sterile border 2-3 mm wide. Pores obscurely stratose, pallid ochre, 2-4 mm deep in each layer, 5-6 per mm, 100-200 µ diameter, dissepiments 50-150 µ thick, most 50-75 µ, apices expanded partly occluding pores, velutinate. Context 2-5 mm thick, ochre or isabelline, of compact intertwined hyphae; skeletal hyphae to 4 µ diameter, lumena almost capillary, sparsely branched, aseptate, staining; generative hyphae to 3 µ diameter, walls 0.2 µ thick, branched, septate. Hymenial layer to 20 µ deep, a close palisade of basidia and paraphyses soon collapsing and partly embedded in mucilage. Basidia clavate, 12-16 x 7-8 µ, bearing 4 spores; sterigmata erect, to 4 µ long. Paraphyses clavate, 8-12 x 5-6 µ. Spores elliptical, 7-10 x 4-5.5 µ, walls smooth, hyaline, 0.1 µ thick, staining slightly.

Australia, Tasmania, New Zealand.

Bark or decorticated wood of dead erect trunks, associated with a white rot.
Plants sometimes exude large drops from the hymenial surface, and occasionally these persist so that pore tissue grows between them; consequently when drops disappear eventually the surface exhibits a pitted or reticulated appearance. From Heterobasidion hemitephrum the species may be separated by the different shape and surface of the pileus, larger spores and absence of an orange zone beneath the cortex. Spores vary in length in different specimens, some not exceeding 6.8 x 3.5-4 µ, in others reaching a length of 10 µ.
Tasmania.
Gadgil, P.D. (in association with Dick, M.A.; Hood, I.A.; Pennycook, S.R.) 2005: Fungi on trees and shrubs in New Zealand. Fungi of New Zealand. 4. Fungal Diversity Press.

Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988

Type: Lignicolous Fungi; Description: Basidiomata perennial, solitary or with pilei overlapping each other, firm and woody, attached by a broad lateral base. Pileus effused-reflexed, sometimes ungulate, applanate, or resupinate, 70–170 mm wide, 30–50 mm thick. Pileus surface concentrically sulcate and ridged, radially fluted, light orange brown, darkening to umber with age. Pore surface with a sterile border 2–3 mm wide, white, becoming dirty brown, pores obscurely stratose, 5–6 per mm. Context pale fawn to ochre, 2–5 mm thick. Hyphal system dimitic. Basidiospores elliptical, 7–10 × 4–5 μm, smooth, hyaline.
Distribution: Northland, Auckland, Coromandel, Waikato, Bay of Plenty, Taupo, Wellington, Nelson, Buller, Westland, Fiordland, North Canterbury, Otago Lakes, Southland.; 1st Record: Lloyd (1915: as Fomes cuneatus).
Significance: None. Causes a white heart rot in the hosts listed but is more often found on dead trees and logs (Gilmour 1966a, as Fomitopsis tasmanica).; Host(s): Beilschmiedia tarairi, B. tawa, Dysoxylum spectabile, Nothofagus menziesii, N. solandri var. solandri, N. solandri var. cliffortioides, Weinmannia racemosa.
Johnston, P.R. 2010: Kew Type Specimens - images and notes from P.R. Johnston, 2010.

Fomes cuneatus Lloyd 1915

[Notes from Kew Type specimen, PRJ 2010] Kew images.

Click to collapse Taxonomic concepts Info

Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Anon.
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Buchanan, P.K.; Ryvarden, L. (1988)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Cunningham, G.H. (1948)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Cunningham, G.H. (1949)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Dingley, J.M. (1969)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Gadgil, P.D. (in association with Dick, M.A.; Hood, I.A.; Pennycook, S.R.) (2005)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Gilmour, J.W. (1965)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Gilmour, J.W. (1966)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Hood, I. A.; Beets, P. N. et al. (2008)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Hood, I.A. (1992)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Hood, Ian A.; McDougal, Rebecca L. et al. (2019)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Lloyd, G.C. (1915)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
McKenzie, E.H.C.; Buchanan, P.K.; Johnston, P.R. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden (1988)
Pennycook, S.R.; Galloway, D.J. (2004)
Flaviporus aroha (G. Cunn.) G. Cunn. 1965
Flaviporus aroha (G. Cunn.) G. Cunn. (1965)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Flaviporus aroha (G. Cunn.) G. Cunn. 1965
Flaviporus aroha (G. Cunn.) G. Cunn. (1965)
Cunningham, G.H. (1965)
Fomes cuneatus Lloyd 1915
Fomes cuneatus Lloyd (1915)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Fomes cuneatus Lloyd 1915
Fomes cuneatus Lloyd 1915
Johnston, P.R. (2010)
Fomes cuneatus Lloyd 1915
Fomes cuneatus Lloyd (1915)
Lloyd, G.C. (1915)
Fomitopsis cuneata (Lloyd) G. Cunn. 1948
Fomitopsis cuneata (Lloyd) G. Cunn. (1948)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Fomitopsis cuneata (Lloyd) G. Cunn. 1948
Fomitopsis cuneata (Lloyd) G. Cunn. (1948)
Cunningham, G.H. (1948)
Fomitopsis tasmanica (Berk.) G. Cunn. 1949
Fomitopsis tasmanica (Berk.) G. Cunn. (1949)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Fomitopsis tasmanica (Berk.) G. Cunn. 1949
Fomitopsis tasmanica (Berk.) G. Cunn. (1949)
Cunningham, G.H. (1949)
Fomitopsis tasmanica (Berk.) G. Cunn. 1949
Fomitopsis tasmanica (Berk.) G. Cunn. (1949)
Cunningham, G.H. (1965)
Heterobasidion tasmanicum (Berk.) G. Cunn. 1965
Heterobasidion tasmanicum (Berk.) G. Cunn. (1965)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Heterobasidion tasmanicum (Berk.) G. Cunn. 1965
Heterobasidion tasmanicum (Berk.) G. Cunn. (1965)
Cunningham, G.H. (1965)
Heterobasidion tasmanicum (Berk.) G. Cunn. 1965
Heterobasidion tasmanicum (Berk.) G. Cunn. 1965
Pennycook, S.R. (1989)
Polyporus tasmanicus Berk. 1859 [1860]
Polyporus tasmanicus Berk. (1859) [1860]
Berkeley, M.J.
Polyporus tasmanicus Berk. 1859 [1860]
Polyporus tasmanicus Berk. (1859) [1860]
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Poria aroha G. Cunn. 1947
Poria aroha G. Cunn. (1947)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Poria aroha G. Cunn. 1947
Poria aroha G. Cunn. (1947)
Cunningham, G.H. (1947)
Trichaptum tasmanicum (Berk.) Teixeira 1994
Trichaptum tasmanicum (Berk.) Teixeira (1994)
Buchanan, P.K.; Ryvarden, L. (2000)
Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
Trichaptum tasmanicum (Berk.) Teixeira 1994
Trichaptum tasmanicum (Berk.) Teixeira (1994)
Teixeira, A.R. (1994)

Click to collapse Collections Info

Australoporus tasmanicus (Berk.) P.K. Buchanan & Ryvarden 1988
[Not available]
39 Link to an external page
Flaviporus aroha (G. Cunn.) G. Cunn. 1965
[Not available]
13 Link to an external page
Fomitopsis tasmanica (Berk.) G. Cunn. 1949
[Not available]
1 Link to an external page
Heterobasidion tasmanicum (Berk.) G. Cunn. 1965
[Not available]
55 Link to an external page
Poria aroha G. Cunn. 1947
[Not available]
1 Link to an external page

Click to collapse Metadata Info

1cb17f03-36b9-11d5-9548-00d0592d548c
scientific name
Names_Fungi
8 February 1995
3 April 2001
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