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Hypoderma bihospitum P.R. Johnst. 1990

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Hypoderma bihospitum P.R. Johnst., New Zealand J. Bot. 28 167 (1990)
Hypoderma bihospitum P.R. Johnst. 1990

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Endemic
Present
New Zealand
Political Region

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P.R. Johnst.
P.R. Johnst.
1990
167
ICN
Hypoderma bihospitum P.R. Johnst. 1990
NZ holotype
species
Hypoderma bihospitum

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bihospitum

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Hypoderma bihospitum P.R. Johnst. 1990

Hypoderma bihospitum was also described from two taxonomically unrelated hosts, Anisotome (Apiaceae) and Uncinia (Cyperaceae) (Johnston 1990). Ascospore sheath structure provides one morphological character to distinguish collections from the two hosts. The sheaths of collections from Undnia are externally finely sculptured, appearing to have numerous small, bubble-like structures embedded within the sheath. Collections from Anisotome have sheaths of similar thickness and size but smooth, with no apparent internal structure.

Hypoderma bihospitum P.R. Johnst. 1990

On Uncinia - PDD 53886 holotype, PDD 48329 (IMI 336644), 49301, 49302, 49303, 49304, 49305, 53883, 53884, 53885 (IMI 336645).
On Anisotome -PDD 45036, 46769, 48456, 48572, 49051, 49129 (IMI 336646), 49292.
Ascomata and conidiomata developing on fallen leaves and dead inflorescence stems, within pale, yellowish areas. These pale areas often surrounded by narrow, black zone lines. In surface view ascomata 0.6-1.2 x 0.3-0.5 mm, broad-elliptic in outline with rounded ends. Unopened ascomata with uniformly black walls. On Uncinia the edge of the ascomata is often not sharply defined, with black stippling in the surrounding host tissue (see notes below). Ascomata open by a single, longitudinal slit, the edge of the opening is lined with a narrow, white, red-brown, or yellow-brown zone. Conidiomata 0.1-0.2 mm diam., circular in outline, brown to dark brown, pustulate.

Ascomata subcuticular. In vertical section upper wall of unopened ascomata up to 30-40 µm wide, narrower toward edges, comprising mostly brown to dark brown, thick-walled cells, darker and thicker-walled along the outside of the wall. In unopened ascomata there is a group of thinner-walled, paler cells in the inner half of the wall along the future line of opening. Inside edge of the wall is lined with a one cell wide layer of hyaline, thin-walled, cylindric to globose cells. In opened ascomata the upper wall is up to 40-80 µm thick near the ascomatal opening, becoming gradually narrower toward the base of the wall, comprising dark brown, thick-walled, angular cells, or becoming very dark, with cellular structure . cured. Exposed face of the broken upper wall is lined with a layer of cylindric, thin-walled, hyaline, 15-20 x 3-5 µm cells. Lower wall 10-15 µm thick, of 2-4 layers of brown, thick-walled, angular to cylindric, 4-10 µm diam. cells.

Paraphyses 1-2 µm diam., undifferentiated or irregularly circinate at apex, embedded in persistent gel, extending 15-20 µm beyond asci. Asci 80-130 x 11-16 µm, clavate, tapering to broad, truncate to slightly rounded apex, indistinct central apical pore, 8-spored, spores extending to base of ascus. ascospores 13-19 x 4.5-6.5 µm (average 15.1 x 5.2 µm), in face view elliptic, uniform in shape to both ends, 0-septate, surrounded by a thick gelatinous sheath.

Conidiomata subcuticular. In vertical section the upper wall is less than 5 µm thick, of dense, dark brown material with no obvious cellular structure. Lower wall 3-5 µm thick, of 1-2 layers of brown, thick-walled, angular to cylindric cells. Lower wall is lined with 1-2 layers of hyaline, thin-walled, cylindric cells on which the conidiogenous layer develops. Conidiogenous cells 7-10 x 2-2.5 µm, more or less flask-shaped, tapering to apex proliferation sympodial, often with two conidia held at apex. Conidia 4-5 x 1 µm, cylindric, straight, ends rounded, 0-septate, hyaline.

CHARACTERISUCS IN CULTURE: Ascospores of PDD 45036 germinated on agar plates after 48 hours. Colonies on OA over 85 mm diam. after 6 weeks, aerial mycelium sparse, cottony, white, agar surface becoming dark brown. Black, globose conidiomata forming near edge of the colony, breaking open to expose the conidial ooze. Conidiogenous cells 7-17 x 2-6 µm, with swollen base with more or less cylindric upper part, sympodial proliferation, often with more than one conidium held at apex. Conidia 4.5-8 x 1-1.5 µm, cylindric, ends rounded, straight, 0-septate, hyaline.

On Uncinia - Northland, Auckland, Coromandel, Taupo, Taranaki, Nelson.
On Anisotome - Taupo, Taranaki, Wellington, North Canterbury, Mid Canterbury.
Dead leaves and inflorescence stems of Anisotome spp. (Umbelliferae), and Uncinia spp. (Cyperaccae).
Ascocarpi elliptici, atri; ascocarpi ruptus paries superior cellulis cylindricis in superficie exposita. Asci 80-130 x 11-16 µm, clavati; ascosporae 13-19 x 4.5-6.5 µm, ellipticae, apex rotundatus, basis rotundata.

ETYMOLOGY: bihospitum = of two hosts; refers to unusual host distribution of this species.

NOTES: H. bihospitum can be distinguished from other New Zealand Hypoderma species by ascospore size and shape, and by ascus shape. Hypoderma species typically have clavate-stipitate asci with an elongate, stalk-like base, with the ascospores confined to the upper part of the ascus. Apart from ascus shape, all other characteristics of the hymenium, and of ascomatal structure and pattern of ascomatal development, conform to the concept of Hypoderma accepted in this study.

The host distribution of H. bihospitum is difficult to explain. When viewed in vertical section the collections on Uncinia tend to have darker upper walls to the ascomata, and, in unopened ascomata, a less well-developed paler zone along the future line of opening. The stippled appearance of the host tissue surrounding the ascomata in the collections on Uncinia is due to the stomatal cavities near the ascomata becoming packed full of dark fungal tissue, and is a feature not found on the collections from Anisotome. Apart from these three somewhat variable features, the collections on the different hosts are indistinguishable both macro- and micromorphologically.

H. bihospitum is the only species of Rhytismataceae found on Anisotome, but both Lophodermium unciniae Johnston and L. breve (Berkeley) de Notaris are also commonly found on Uncinia (Johnston 1989).

NORTHLAND, Puketi State Forest, Waiohanga Tr., on Uncinia uncinata (Linn. f.) Kirk., coll. P. R. Johnston (R735), 23 Oct 1987 (PDD 53886).

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Hypoderma bihospitum P.R. Johnst. 1990
Hypoderma bihospitum P.R. Johnst. 1990
Hypoderma bihospitum P.R. Johnst. 1990
Hypoderma bihospitum P.R. Johnst. (1990)
Hypoderma bihospitum P.R. Johnst. 1990
Hypoderma bihospitum P.R. Johnst. (1990)
Hypoderma bihospitum P.R. Johnst. 1990
Hypoderma bihospitum P.R. Johnst. (1990)

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Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Auckland
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Coromandel
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Mackenzie
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Mid Canterbury
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Nelson
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
North Canterbury
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Northland
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Taranaki
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Taupo
Hypoderma bihospitum P.R. Johnst. 1990
New Zealand
Wellington

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taxonomic status
Probably two seperate host-specialised species have been labelled L. bihospitum the type is the species from Unicinia. [PRJ]

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1cb18e6c-36b9-11d5-9548-00d0592d548c
scientific name
Names_Fungi
10 September 1993
15 December 2003
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