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Chlorovibrissea phialophora Samuels & L.M. Kohn 1989

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Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
Chlorovibrissea phialophora Samuels & L.M. Kohn 1989

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Endemic
Present
New Zealand
Political Region

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Samuels & L.M. Kohn
Samuels & L.M. Kohn
1989
116
ICN
Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
NZ holotype
species
Chlorovibrissea phialophora
HOLOTYPE. New Zealand. North Island. Auckland: Waitakere Ranges, Waitemata City, across rd. from Nihotupu Dam, on decaying Leptospermum sp., 1 Sep1982, Johnston ( PDD 46963; isotype, CUP ).

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phialophora

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Chlorovibrissea phialophora Samuels & L.M. Kohn 1989

See Manaaki Whenua datastore https://doi.org/10.7931/KEZ8-4342, Chlorovibrissea sensu Sandoval-Leiva et al. 2014 is polyphyletic

Chlorovibrissea phialophora Samuels & L.M. Kohn 1989

ADDITIONAL SPECIMEN EXAMINED. NEW ZEALAND. NORTH ISLAND. AUCKLAND: Waitakere Ranges, vic. Swanson, Auckland University Tramping Club Hut, on decaying wood of Leptospermum sp., 24 Aug 1982, Samuels et al (PDD 46964).
Ascomatal Morphology. Apothecia 10-30 mm high, gregarious, stipitate-capitate, produced from a green, pulvinate, mycelial pad 1.5-2.0 mm diam. on the surface of nonblackened wood; stipe 10-25 mm long x 1 mm diam., green, villose or glabrous, longitudinally or spirally furrowed, circular in section; cap subglobose to cylindrical, 2-7 mm high x 2-5 mm wide, dark green to nearly black, smooth, viscid or appearing gelatinous at maturity, separated from stipe by a distinct groove; groove not apparent at maturity; ascomata leaching an olivaceous pigment in 10% KOH. Ascomatal Anatomy. Asci 8-spored, (100-) 105-116(-123) x 5-6 µm, produced from croziers, narrowly clavate to cylindrical, tapering toward the base and there forming a small foot; apical ring intensely J + in Melzer's reagent, with a "crown" of intense staining in methyl blue or phloxine just below apical ring; ascospores fillings, each ascus. Ascospores (35.0-) 42.0-51.6 (-60.0) x 1.0-1.5 µm multiseriate, hyaline; filiform, tapering slightly from rounded apex to pointed base, 0-1-septate; apical cell enlarging while still in ascus and forming a subglobose to cylindrical phialide, collarette cupulate, ca. 1.5 µm deep; length of phialide from apex to first septum of ascospore (9-)10-17(-20) µm; spore eventually elongating to 85 µm, all cells of spore enlarging, phialide arising only from apical cell. Ascoconidia arising from phialides, 1.7-4.0(-5.0) x 1.0-1.5 µm, oblong, lacking a basal abscission scar, eguttulate, hyaline. Paraphyses extending beyond asci by ca. 10 µm, hyaline, unbranched, not anastomosing, filiform, 2-3 µm broad, Septate, apical cell ca. 40 µm long, subsequent cells ca. 20 µm long, tip clavate to subglobose, 4-5 µm. Subhymenium poorly developed, consisting of tightly interwoven, narrow, nonpigmented hyphae. Medullary excipulum composed of textura intricata, hyphae 3-4 µm broad with walls 0.5 µm thick, becoming gelatinized at maturity, continuous with medulla of stipe; zone adjacent to subhymenium turning green in Melzer's reagent. Ectal excipulum poorly developed, forming a thin, ca. 80 µm wide layer on underside of cap, composed of prosenchyma with the long axis of cells parallel to the excipular surface, cells 25-35 µm long x ca. 8 µm broad, walls 1.0-1.5 µm thick, cells producing hyphal hairs up to 30 µm long x surface cells producing hyphal hairs up to 30 µm long x 4-5 µm broad, septate, pale green; ectal excipulum continuing down stipe for a distance of ca. 200 µm. Stipe lacking a well-developed cortex, hyphae continuous with medullary excipulum, with refractive, gelatinized walls; stipe hollow at maturity; cells at surface of stipe 6-8 µm, somewhat broader than those within, producing hyphal hairs, hairs 25-35 µm long x ca. 8 µm broad, septate, infrequently branched, pale green, forming a fine tomentum over surface of stipe, absent at maturity. Mycelial pad from which stipe arises composed of interwoven, septate, branched, green hyphae 3-4 µm broad and to 100 µm long, with many free ends giving pad a wooly aspect.
Ascomata stipitato-capitata, melanochlora, 10-30 mm alta. Capitis 2-7 mm altis x 2-5 latis. Stipitibus 10-25 mm longis x ca. 1 mm diam. Asci anguste clavati vel cylindrici, (100-)105-116(-123) x 5-6 µm; apice cum annulo iodo coerulescenti. Ascosporae filiformes, (35.0-) 42.0-51.6 (-60.0) x 1.0-1.5 µm, 0-1-septatae; apice cum phialide instructo; phialide (9-)10-17(-120) µm longa, Phialophora-simili. Ascoconidia oblonga, 1.7-4.0(-5.0) x 1.0-1.5 µm, hyalina.
Chlorovibrissea phialophora differs from the other three species, C tasmanica, C melanochlora, and C. bicolor, in producing ascoconidia and in turning green in a narrow zone of the medullary excipulum adjacent to the subhymenium. Chlorovibrissea tasmanica has narrower paraphysis apices, narrower ectal excipular cells, and a more luxuriant tomentum on the stipe composed of longer hyphal hair than in C. phialophora. Chlorovibrissea melanochlora produces longer ascospores, asci, and stipe hairs, and narrower ectal excipular cells. Chlorovibrissea bicolor produces longer ascospores which are apically coiled in the ascus, narrower paraphysis apices, narrower ectal excipular cells, and longer hyphal hairs.

The formation of ascoconidia is not uncommon in the Helotiales. Species of Geoglossum Pers.: Fr., Cudonia Fr., Spathularia Pers. (Berthet, 1964), Ascocoryne Groves & Wilson (Roll-Hansen & Roll-Hansen, 1979), Tympanis Tode: Fr. (Groves, 1952), and Rutstroemia Karsten (White, 1941) among others, are known to produce conidia from ascospores still in the ascus. Conidiogenesis in C. phialophora is unusual because the tip of the ascospore is converted into a more or less complex phialide. In the other genera, conidia are produced laterally or terminally on barely differentiated conidiogenous loci. Discharged ascospores of Encoelia pruinosa (Ell. & Everh.) Torkelson & Eckblad sometimes produce phialidic openings through which microconidia develop (Juzwik & Hinds, 1984), and phialides arise directly from the surface of discharged ascospores of some species of Rutstroemia (White, 1941).

New Zealand. North Island. Auckland: Waitakere Ranges, Waitemata City, across rd. from Nihotupu Dam, on decaying Leptospermum sp., 1.Sep 1982, Johnston (PDD 46963; isotype, CUP).

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Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
Chlorovibrissea phialophora Samuels & L.M. Kohn (1989)
Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
Chlorovibrissea phialophora Samuels & L.M. Kohn
Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
Chlorovibrissea phialophora Samuels & L.M. Kohn (1989)
Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
Chlorovibrissea phialophora Samuels & L.M. Kohn (1989)

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Chlorovibrissea phialophora Samuels & L.M. Kohn 1989
[Not available]

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typification
HOLOTYPE. New Zealand. North Island. Auckland: Waitakere Ranges, Waitemata City, across rd. from Nihotupu Dam, on decaying Leptospermum sp., 1 Sep1982, Johnston ( PDD 46963; isotype, CUP ).

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1cb1826f-36b9-11d5-9548-00d0592d548c
scientific name
Names_Fungi
7 October 1998
9 January 2003
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