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Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004

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Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004

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Endemic
Present
New Zealand
Political Region

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(Berk.) R.H. Petersen
Berk.
R.H. Petersen
2004
99
ICN
species
Lentinellus novae-zelandiae

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novae-zelandiae

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Lentinus Novae-Zelandiae, Berk.; minor, subimbricatus, pileo flabelliformi tenui rufo-badio postice velutino, lamellis angustis tenuibus pileo concoloribus. HAB . On dead wood, Colenso. Subimbricated. Pileus 1 inch or more long and broad, thin, flabelliform, suborbicular or reniform, bay-brown, clothed behind with short velvety olive down. Stem obsolete. Gills of the same colour as the pileus, narrow, decurrent behind ; edge thin, lacerated. Closely resembling Lentinus castoreus, of which I have an authentic specimen, but differing in size and in the narrow gills.
Sessile, attached by a narrowed base, fan-shaped, reniform or suborbicular, thin and flexible, bay-brown, clothed behind with short velvety olive down, about 2.5 cm. long and broad; gills decurrent behind, narrow, edge thin and torn, coloured like the pileus.
New Zealand.
On dead wood.
Closely resembling Lentinus castoreus, but smaller, and with narrower gills. There is no specimen in Berkeley's herbarium.

Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004

Specimens examined ARGENTINA, Prov. Neuquen, vie. Puerto Manzano, "Cerro Cortinario," 15.111.63, coll. R. Singer (as L. omphalomorphus), no. M3059 (MICH ex BAFC); Prov. Tierra del Fuego, Dpto. Ushuaia, Tierra Mayor, 5.111.74, Horak 74/149 (isotype; ZT); Tierra Mayor, 1975, Horak no. 75/77 (ZT); Valle Glaciar Martial, vie. Ushuaia, 1975, Horak no. 75/40 (ZT). NEW ZEALAND, North Island, Auckland, Waitakere Ranges, Waiatarua, 26.VII.72, coil. J.M. Dingley, det. B.P. Segedin (as L. marginatus), no. 63250 (PDD); Bay of Plenty, Mamaku Ranges, 5.IV.65, coll. R.F.R. McNabb, det. B.P. Segedin (as L. pulvinulus), no. 62528 (PDD); South Island, South Canterbury, Peel Forest, 22.VII.67, coll. G.M. Taylor (GMT 374), det. B.P. Segedin (as L. marginatus; holotype), no. 63251 (PDD); Nelson Dist., St. Amaud, Lake Rotoiti Lodge, Peninsula Track, coll. G. Ridley, on Nothofagus, det. B.P. Segedin (as L. pulvinulus), TFB 7104 (TENN 56878).

Basidiomata gregarious, flabelliform, spathulate, ligulate when young to subdimidiate when mature, convex to subconchate, sessile to pendent (i.e. not everted-curled like L. cochleatus). Pileus 7-32 mm broad, up to 24 mm deep, subundulate to delicately radially rivulose, "Rood's brown" to "pecan brown" (6C5-6135), russet to (where poorly dried) brown-black, "orange buff' to "capucine buff' (5A5-6) or duller (5B5-7), with spots of "buckthorn brown" (5136), surface smooth outward, minutely pubescent to minutely micaceous at disc, more hirsute or hoary at stipe attachment; hoary ornamentation yellow, drying pallid gray; margin translucent-striate, decurved, fimbriate to crenulate but not striate, darker than pileus, as though hygrophanous (5B5); flesh thin (less than 1 mm thick). Lamellae adnate, subdecurrent, subdistant, up to 3.5 mm deep, in at least three ranks, "pale cinnamon pink" (5A2-3) to "cinnamon buff' when fresh, drying to "tilleul buff'.to (poorly dried) dark brown (5135, 6C4); margin coarsely digitate-serrate, reported as minutely white. Stipe lateral to absent, 2-10 X 2-4 mm, prominent, reduced to a knot or absent, more or less equal (when present), irregular in cross-section (i.e. not terete, fluted by lamellar ridges), near "buckthorn brown" (5137), dark brown, "drab," to "light drab," strigose, plushy to covered with hyphal spikes. Odor very weak, typical; taste very slowly weakly acrid, mildly anesthetic to tip of tongue.

Pileipellis a repent, radial, coherent layer of generative hyphae involved in mucus; hyphae 2.0-7.0 µm diam, hyaline to yellowish brown (BF, KOH), thin-walled, clamped; mucus epi- and interhyphal, discharged in globules in squash mounts (PhC, KOH), amorphous, not granular. Suprapellis outward undeveloped but lanceolate pileicystidia emergent from generative hyphae; pileicystidia (Fig. 24) 55-92 X 6.7-13.0 µm, ranging from elongate-ellipsoid with bluntly rounded apex to fusoid with prolonged beak, to fusiform-lanceolate, gradually tapered to bluntly lanceolate tip, hyaline, sometimes biaxial, thin-walled, inamyloid; inward pileicystidia gloeoplerous, 150-340 X 6.5-17.0 µm, narrowly vermiform to nematoform, tapering to narrow apex, undulate to irregularly swollen, thick-walled (wall up to 1.8 µm thick), yellow-refringent (PhC, KOH), inamyloid; contents glassy to finely coscinoidal; pileileptocystidia numerous, 2.0-3.0 µm diam, hyaline, filamentous, rounded at apex, twisted to delicately undulate, emergent up to 45 µm. Subpellis of outer pileus dimitic: 1) generative hyphae 3.0-6.0 µm diam, hyaline, thin-walled, clamped; and 2) gloeoplerous hyphae abundant, sinuous, yellow-refringent (PhC, KOH); contents cosdinoidal; subpellis of inner pileus dimitic: 1) generative hyphae undulate, thick-walled (wall up to 0.7 µm thick), hyaline, clamped; and 2) gloeoplerous hyphae occasional, as in outer subpellis.

Pileus trama interwoven, dimitic: 1) generative hyphae 2.0-7.5 µm diam, hyaline, thick-walled (wall up to 1.3 µm thick, commonly occluding cell lumen), glassy-refringent over short lengths, long-celled, branched, inamyloid to weakly amyloid (pale blue-gray), conspicuously and frequently clamped, occasionally ornamented with minute warts on exterior surface and then appearing minutely banded; and 2) gloeoplerous hyphae common (not abundant) near surface, less so inward, 3.5-7.0(-14.0) µm diam, yellow-refringent (PhC, KOH), thin-walled, emergent up to 15 µm; and 4) leptocystidia (Fig. 25c) filamentous, 1.8-3.0 µm diam, yellow-refringent (PhC, KOH), emergent up to 15 µm; contents coscinoidal.

Basidiospores (Fig. 25d) 4.0-5.7 X (3.5-)4.0-4.5 µm (E = 1.08-1.33; Em = 1.20; Lm = 4.85 gym), ovate to broadly ovate to subglobose, thin-walled, weakly to moderately amyloid; ornamentation of densely scattered, strongly amyloid prickles barely visible at 1500X;contents homogeneous to uniguttulate.

New Zealand, Patagonia, Tierra del Fuego.
Habitat: on standing or fallen rotten wood in a mixed Nothofagus/Podocarpus forest
Commentary Although centrally to eccentrically stipitate basidiomata of L. singeri are found (see-Horak, 1979), some basidiomata closely resemble those of L. fabelliformis and/or L. occidentalis (laterally stipitate; pileus broadly cuneiform to subdimidiate). In this feature, however, basidiomata are not of the everted-curled stature of members of the L. cochleatus complex.
Neither pleurocystidia nor pileicystidia can be reliably referred to generative or gloeoplerous hyphal systems. Neither structure could be traced to a gloeoplerous hypha and contents appeared hyaline and homogeneous under phase contrast microscopy. Horak correctly illustrated pileicystidia as basally bifurcate, assumedly arising from generative hyphae of the subpellis or trama. Nonetheless, occasionally cell contents are less than homogeneous, but subtly multigranular as though gloeoplerous. In L. tridentinus, pileicystidia are definitely gloeoplerous in color and light refringence, and differ in form (pileicystidia vermiform in L. tridentinus; hymenial cystidia clavate to bluntly rounded).
A molecular phylogenetic reconstruction places L. singeri as virtually congruent with L. marginatus ss Segedin (q.v.). The two species share several rather unique characters: 1) attachment to substratum; 2) small basidiomata; 3) minutely micaceous appearance of inner pileus surface (30X); 4) similar pileal pseudocystidia; 5) subdistant, coarsely serrate lamellae; 6) relatively large basidiospores. Examination of the few available specimens of each species lead us to conclude that they are conspecific.
Horak (1979) referred to Lentinellus omphalomorphus (Bertero & Montagne) ss. Singer as a synonym of L. singeri, but presented no evidence of how "ss. Singer" differed from the original descriptions and/or specimen by Montagne. Likewise, no evidence was reported about why the taxon required a new name unless "ss Singer" could be shown not to agree with the original material.
Nonetheless, L. singeri was given as "sp. n." by Horak, not as "nom. nov." as would have been required if Agaricus omphalomorphus Bert. apud Mont. had been a later homonym. Likewise, Singer (1969) recombined Agaricus omphalomorphus in Lentinellus, and while citing several Singer collections, did not report examination of Montagne's type specimen. We were unable to examine Montagne's type specimen (PC), so the identity of Montagne's organism remains in doubt, and the correlation of Singer's sense of the name cannot be ascertained without examination of all pertinent material. Until this has been accomplished, we are reluctant to repeat doubtful synonymy.
Although we have examined the specimens which Segedin (1996) cited under L. marginatus, we have been unable to observe the "chlamydospores" described and figured by Segedin. Instead, the only structures which could be construed as such were skeletalized pileicystidia near the pileus margin, elongate-ellipsoid in outline but never disarticulated. Moreover, Segedin (1996) described L. marginatus even after having examined the type specimen of Lentinus novaezelandiae, apparently based on the putative chlamydospores in L. marginatus.
Some basidiomata of L. novaezelandiae are virtually indistinguishable from those of L. occidentalis. Those of the latter are also characterized by pileicystidia of comparable dimensions to those of L. novae-zelandiae, and spore statistics are not significantly different. DNA sequences, moreover, show L. occidentalis to be in a clade with L. montanus and closely related to L. novae-zelandiae.
Although dimitic, generative hyphae of the pileus trama in L. novae-zelandiae are often skeletalized and then sometimes faintly amyloid. This construction is quite like that of L. fabelliformis, basidiomata of which are similar to those of L. novae-zelandiae. Pileicystidia are absent in L. fabelliformis, however, and the species is known to occur only in the North Temperate Zone.
MATERIAL EXAMINED: NEW ZEALAND: South I.: South Canterbury, Peel Forest, G. M. Taylor, 22 Jul 1967, GMT 374 PDD 63251(holotype). North I.: Auckland, Waitakere Ra., Waiatarua, on rotten, standing tree, J. M. Dingley, 26 Jul 72, PDD 63250.
Basidioma convex, dimidiate to ligulate, sessile or laterally stipitate. Pileus 10-25 mm diam. (dry measurement), dull pinkish-fawn when fresh (G. M. Taylor field notes), when dried greyish-orange, sahara, sienna (6C5-6D5 K&W), darker at the margin, surface smooth, sometimes with scattered, minute white to buff hairs near the stipe attachment, margin inrolled, lacerate. Lamellae pale pinkish-fawn when fresh (G. M. Taylor field notes), with a white margin (J. M. Dingley field notes), drying yellowish-brown (6C4 K&W), relatively broad, moderately distant, in three series, adnate to decurrent, edge broadly lacerate. Stipe when present lateral, small, button-like or up to 10 mm long by 3 mm broad, cylindrical, typically clothed in a tangled tomentum through which protrude dark red-brown to black bristly hairs, up to 2 mm long, particularly noticeable in older basidiomata. Taste and smell unknown. Spore print white, becoming cream.
Spores 4.0-5.5 x 3.5 4.5 (4.9 x 4.0) µm, Q = 1.2, subglobose, hyaline, wall strongly amyloid, with short peg-like ornamentation and distinct apiculus. Basidia 20 - 30 x 6 µm, clavate, mostly 4-spored, sometimes 2-spored, each with clamp connection on basal septum. Leptocystidia plentiful on all parts of the lamellae, mostly subulate, narrowly to broadly fusiform or narrowly lageniform, 30-60 x 3 - 12 µm, thin-walled, usually without contents and each with a clamp connection at the base. A few clavate to lanceolate pseudocystidia also present. Trama of more or less parallel, thin-walled, clamped, descending hyphae, up to 3 µm diam. Many parallel, oleiferous hyphae present, 3-5 µm diam., becoming contorted, with some empty segments and slight epimembranal incrustation, near the very narrow, cellular sub-hymenium. No thick-walled hyphae in trama. Trama ochraceous in KOH, negative in Melzer's reagent. Context of interwoven hyphae, relatively thin-walled, up to 6 µm diam., with plentiful oleiferous hyphae concentrated particularly near the pileipellis. Oleiferous hyphae up to 7 µm diam., often much contorted and with swellings up to 14 µm diam. Skeletal hyphae absent. Middle region of context dextrinoid but colour fades fairly quickly. Pileipellis of repent, interwoven, yellowish-brown, thin-walled hyphae, 2 - 3 µm diam., with many interspersed oleiferous hyphae, the ends of which protrude as numerous pseudocystidia, especially near the stipe attachment. Pseudocystidia clavate, lageniform or lanceolate, 50- 90 x 12 - 13 µm, walls only slightly thickened at first but those towards the stipe becoming thick-walled. Sections through the margin of the pileus show clusters of clavate cells 20-30 x 5 - 7µm, intermingled with basidia and pseudocystidia. The apices of these clavate cells become converted into thick-walled chlamydospores, subpyriform when first produced but after secession becoming subspherical, 5.5-8.0 x 4.5-6.5 (7.15 x 5.8) µm, Q = 1.2, with walls up to 3 µm thick, inamyloid, not dextrinoid. Stipe of more or less parallel hyphae up to 3 µm diam. with slightly thickened walls, together with oleiferous hyphae of slightly larger diameter and some thick-walled hyphae up to 6 µm diam., with walls up to 2 µm. Surface tomentum of stipe of tangled, hyaline, branched, narrow (up to 2 µm) clamped hyphae, mixed with oleiferous hyphal endings and a few fusiform leptocystidia; chlamydospores, detached from the margin of the pileus, are commonly found adhering to the tomentum hyphae, but never seen with a germ tube. The tough, bristly hairs up to 2 mm long that protrude through the tomentum consist of narrow (1-2 µm diam.), slightly thick-walled, brown, agglutinated hyphae, with occasional clamp connections.
HABITAT: on standing or fallen rotten wood in a mixed beech/podocarp forest, disturbed, with some adventives.
Basidiomata convexa, dimidiata vel ligulata, sessilia vel lateraliter stipitata. Pileus 10 25 mm latus, sordide subroseo-bubalinus (vivus), griseo-aurantiacus vel senatus (6C5-6D5 K&W, exsiccatus), superficie glabra, interdum cum pilis pallidis, minutis, conspersis apud stipitem; margine involuta, erosa. Lamellae dilute subroseo-bubalinae (vivae), argillaceae (exsiccatae) latiusculae, moderate distantes, dispersae in seriebus tribus, margine lacerata, alba. Stipes lateralis, statura variabilissimus, ad 10 mm longus, 3 mm latus, aequus, vestitus tomento implicato, cum setis ad 2 mm longis, tenacibus, roseobrunneis vel atris. Odor saporque incogniti. Imago sporarum alba. Sporae 4-5.5 x 3.5-4 (4.9 x 4) µm, Q - 1 2, subglobosae, hyalinae, amyloideae fortiter, echinulatae, apiculo prominenti. Basidia 20-30 x 6 µm, clavata, plerumque tetraspora, saepe bispora, fibulata. Leptocystidia multa in omnibus partibus lamellarum, subulata, fusiformia, lageniformia, 30 - 60 x 3 - 12 µm, parietibus tenuibus, apice acuta, fibulatis, cavis. Pseudocystidia clavata vel lanceolata adsunt. Trama ex hyphis, parallelis, descendentibus, ad 3 µm latis, parietibus tenuibus, fibulatis; multae hyphae oleosae 3 - 5 µm diam. adsunt, parallelae in trama media, contortae in trama laterali. Subhymenium angustissimum. Hyphae incrassatae desunt. Trama ochracea in KOH, nec amyloidea nec dextrinoidea. Contextus ex hyphis intertextis cum parietibus tenuibus, angustis (ad 6 µm diam.), cum multis hyphis oleosis (ad 7 µm) cum tumoribus paucis. Hyphae incrassatae desunt. Pileipellis ex hyphis repentibus, bubalinis, angustis (2 - 3 µm diam.), intertextis, parietibus subincrassatis, cum multis hyphis oleosis sub superficie. Hyphae oleosae protrudentes per pellem pro pseudocystidiis. Pseudocystidia clavata, versiformia, lageniformia vel lanceolata, 50-90 µm longa, 12 - 13 µm lata, parietibus tenuibus, incrasscentibus. In margo pileipellis, cellulae fasciculatae, clavatae, 40-60 x 10 - 14 µm, cum basidiis et pseudocystidiis intermixtis. Apices cellularum in chlamydosporas transformantes. Chlamydosporae cum parietibus incrasscentibus ad 3 µm diam., primo subpyriformes (5-5.8 x 4.5-6.5µm, Q = 1.2), subglobosae post secessionem, hyalinae, nec amyloideae nec dextrinoideae. Stipes ex hyphis subparallelis, ad 3 µm diam., cum hyphis oleosis et hyphis paucis incrasscentibus. Tomentum stipitis ex hyphis implicatis, angustis, ramosis, cum pseudocystidiis et leptocystidiis fusiformibus paucis. Chlamydosporae exutae ex margine pilei saepe hyphis tomenti adhaerentes inveniuntur. In basidiomatis veterioribus pili tenaces longi (ad 2 mm.), ex hyphis longis, angustis, brunneis, agglutinatis, protrudentes per tomentum. Ad lignum putridum in silva. Novae-Zelandiae.

ETYMOLOGY: Referring to the chlamydospores on the margin of pileus and the white edge of the lamellae.

The production of chlamydospores on the margin of the cap is a very distinctive character in Lentinellus marginatus. L. cochleatus seems to be the only other species reported to produce chlamydospores but they are described as being either on the stipe (Miller & Stewart 1971) or formed interstitially beneath the pileipellis (Breitenbach & Kranzlin 1991). Also, the basidiomata of L. cochleatus are different in form, with well developed, long stipes in tightly fused caespitose clusters (Miller & Stewart 1971).

HOLOTYPUS: PDD 63251

Shown to be a synonym of Lentinellus ursinus by Pegler 1983.

Berkeley's (1855) description is "Subimbricated. Pileus 1 inch or more long and broad, thin, flabelliform, suborbicular or reniform, bay brown, clothed behind with short velvety olive down. Stem obsolete. Gills same colour as the pileus, narrow, decurrent behind; edge thin, lacerated. Closely resembling L. castoreus, of which I have an authentic specimen, but differing in size and narrow gills."
The type material (New Zealand: Colenso, Herb. Phillips, ex Herb. Berkeley, K) consists of 4 basidiomata up to 26 x 17 mm diam. Their characters all confirm Pegler's identification of the species as yet another synonym of L. ursinus.

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Lentinellus marginatus Segedin (1996)
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
Lentinellus novae-zelandiae (Berk.) R.H. Petersen (2004)
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
Lentinellus novae-zelandiae (Berk.) R.H. Petersen (2004)
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
Lentinellus novae-zelandiae (Berk.) R.H. Petersen (2004)
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
Lentinus novae-zelandiae Berk. (1855)
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004

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New Zealand
South Canterbury
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
New Zealand
Auckland
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
New Zealand
Bay of Plenty
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
New Zealand
Buller
Lentinellus novae-zelandiae (Berk.) R.H. Petersen 2004
New Zealand
Fiordland

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taxonomic status
Sequence data suggests this is an earlier name for L. occidentalis [JAC]

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e5906265-269c-4061-9f65-e4e01f0f29a7
scientific name
Names_Fungi
17 December 2003
29 November 2006
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