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Valsalnicola oxystoma - Fungal Planet

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148 Persoonia – Volume 29, 2012<br />

<strong>Valsalnicola</strong> <strong>oxystoma</strong><br />

a<br />

b<br />

c<br />

d<br />

e


<strong>Fungal</strong> <strong>Planet</strong> description sheets<br />

149<br />

<strong>Fungal</strong> <strong>Planet</strong> 128 – 20 December 2012<br />

<strong>Valsalnicola</strong> D.M. Walker & Rossman, gen. nov.<br />

Etymology. Named for its valsa-like appearance and occurrence on<br />

species of Alnus.<br />

Causing linear cankers and lesions. Ectostromata well-developed,<br />

brown to black, thick disc from which perithecial necks<br />

emerge. Ascomata perithecial, immersed beneath ectostroma,<br />

aggregated in groups of 13–23, converging into 5–20 necks.<br />

Asci fusiform, with indistinct apical ring. Ascospores allantoid<br />

with rounded ends, 1-septate, hyaline.<br />

Type species. <strong>Valsalnicola</strong> <strong>oxystoma</strong>.<br />

MycoBank MB801277.<br />

<strong>Valsalnicola</strong> <strong>oxystoma</strong> (Rehm) D.M. Walker & Rossman, comb. nov.<br />

Basionym. Valsa <strong>oxystoma</strong> Rehm, Ber. Naturhist. Vereins Augsburg 26:<br />

70. 1881.<br />

≡ Cryptodiaporthe <strong>oxystoma</strong> (Rehm) Z. Urb., Preslia 29: 395. 1957.<br />

Twig lesions in surface view (511–)591–890(–893) µm diam<br />

(mean = 654, S.D. 122, n = 13). Ectostroma well-developed,<br />

brown to black, thick disc from which perithecial necks emerge.<br />

Ascomatal cavity (690–)765–909(–950) µm high × (1610–<br />

)1710–2346(–3947) µm diam (mean = 816 × 2198, S.D. 109,<br />

703, n1 = 5, n2 = 9). Ascomata perithecial, immersed beneath<br />

ectostroma, causing host tissue to swell and rupture, perithecia<br />

converging into 5–20 necks, emerging at surface through<br />

ecto stromatic disc, perithecia grouped 13–23. Ascomata<br />

glossy black, subglobose to globose (240–)266–298(–320)<br />

µm high × (253–)260–335(–337) µm diam (mean = 282 × 294,<br />

S.D. 25, 36, n1 = 7, n2 = 13); necks central, straight to curved,<br />

length (426–)428–550(–563) µm (mean = 476, S.D. 54,<br />

n = 9). Asci fusiform, (38–)39–48(–49) × (8–)9–12(–13) µm<br />

(mean = 44 × 11, S.D. 4, 1.2, n1 = 17, n2 = 18), apex broadly<br />

rounded, with indistinct apical ring, stipe acute, rounded, or tapering<br />

to a point, ascospores arranged irregularly multiseriate.<br />

Ascospores allantoid with rounded ends, mostly curved, rarely<br />

straight, (9–)10–11(–12) × 2–3 µm (mean = 11 × 2, S.D. 0.9,<br />

0.5, n = 30), 1-septate, median, slightly constricted or not at<br />

septum, each cell with several small guttules, hyaline. Cultures<br />

slow-growing, 3–6 mm in 10 d on potato-dextrose agar, mycelium<br />

low, pale brown to greyish brown, reverse dark brown.<br />

In culture on synthetic nutrient-poor agar — Dimorphic,<br />

forming a synanamorph. Conidiomata pycnidial, exuding<br />

masses of brown conidia. Conidiophores reduced to conidiogenous<br />

cells, or one supporting cell, proliferating percurrently.<br />

Conidia cylindrical, brown, finely verruculose, apex obtuse,<br />

base truncate, 3–5-euseptate, 15–23 × 4–5 µm. Conidia of<br />

synanamorph intermingled in same conidioma, but conidiogenous<br />

cells proliferating percurrently or sympodially; conidia<br />

hyaline to subhyaline, narrowly obclavate, apex subobtuse,<br />

base truncate, straight to curved, 25–80 × 2.5–3 µm, up to<br />

11-septate. Synanamorph also developing in aerial mycelium<br />

(on PNA); conidiophores subcylindrical, straight to curved,<br />

0–2-septate, hyaline to subhyaline, 8–15 × 2–3 µm, proliferating<br />

sympodially at apex. Conidiophores solitary or fasciculate<br />

or on a reduced stroma.<br />

Colour illustrations. Italy, Trentino, Val Sadole, showing trees of Alnus<br />

viridis with green alder decline (Giorgio Maresi). a. Rehm: Ascomyceten 280,<br />

scale bar = 500 µm. b–d. BPI 884137, scale bars of perithecia = 100 µm,<br />

scale bar of ascus = 10 µm. e. Rehm: Ascomyceten 280, scale bar = 10 µm.<br />

Typus. Austria, Tyrol, Längenfeld, on dead branch of Alnus viridis,<br />

c. 3 500 ft., Aug. 1874, coll. Rehm. This type specimen was issued as<br />

Rehm, Ascomyceten no. 280. Of the two specimens at BPI, the more plentiful<br />

one is in the bound set of Rehm, Ascomyceten, and is herein designated<br />

as Lectotype BPI 884138. Isolectotypes examined BPI 738235 and NY,<br />

MycoBank MB801277.<br />

Additional specimens examined. Belgium, Brussels, Soignes, on branch<br />

of Alnus glutinosa, Oct. 1899, P. Nypels, comm. H. Rehm, Vestergren,<br />

Micro mycetes rariores selecti 409 as Valsa <strong>oxystoma</strong> (BPI 574854). – Canada,<br />

British Columbia, Yoho National Park, Chancellor Mountain Camp, on<br />

Alnus sp., 11 Aug. 1962, R.F. Cain, TRTC 40116 (NY); Ontario, Kenora<br />

District, Tustin Township, Gordon Lake, Rd., on Alnus sp., 26 Sept. 1959,<br />

coll. D. Bowen, det. J. Reid as Valsa <strong>oxystoma</strong> (BPI 574855). – Italy, Trento,<br />

Monte Bondone Trento, E11°03'51" N46°02'20", on Alnus viridis, Apr.<br />

2011, G. Maresi, isol. A. Rossman AR 4833 = CBS 133337, ITS sequence<br />

JX519559, and LSU sequence JX519563 (BPI 884137); Trento, val Sadole<br />

(E11.60, N46.15), 2009, G. Maresi & C.M.O. Longa (BPI 884136). – Sweden,<br />

Umea, on dead branch of Alnus ‘borealis’, Sept. 1910, Vlengel, det.<br />

F. Bubak (BPI 574856). – USA, Alaska, near Fairbanks, Moose Creek, Environmental<br />

Monitoring Plot 316 MC UM11 MRC, N64.72, W147.23, elev.<br />

150 m, on Alnus incana var. tenuifolia, May 2010, G.C. Adams, culture AR<br />

5137 = CBS 133329, ITS sequence JX519561 (BPI 884135).<br />

Habitat — Alnus viridis ssp. viridis, causing a twig colonization<br />

and canker disease involved in green alder decline (Pisetta<br />

et al. 2012); also known from Alnus glutinosa, A. incana,<br />

A. incana var. tenuifolia, A. rubra, A. viridis ssp. fruticosa and<br />

A. viridis ssp. maximowiczii.<br />

Distribution — Asia: Japan (Kobayashi 2007); Europe: Austria,<br />

Belgium, Italy, Sweden, also United Kingdom (Cannon et<br />

al. 1985); North America: Canada (Ontario); USA: Alaska.<br />

Notes — <strong>Valsalnicola</strong> is based on a species that was described<br />

in the genus Valsa. Although it resembles Valsa in<br />

having allantoid ascospores, the ascospores of <strong>Valsalnicola</strong><br />

are 1-septate while the majority of species of Valsa and closely<br />

related Leucostoma and Valsella have aseptate ascospores.<br />

However, one species of Valsa, V. melanodiscus, also has<br />

1-septate ascospores, occurs on Alnus spp., and produces linear<br />

cankers on the host. A distinguishing feature of <strong>Valsalnicola</strong><br />

is the lack of a black line surrounding stromata in the ascomatal<br />

cavity, which is characteristic of Valsa melanodiscus. In<br />

addition, the growth rate of cultures of <strong>Valsalnicola</strong> <strong>oxystoma</strong><br />

is considerably slower than species of Valsa. Molecular sequence<br />

data place this new genus within the Gnomoniaceae-<br />

Melanconidaceae complex. Allantoid, 1-septate ascospores<br />

have not previously been reported in the Gnomoniaceae or<br />

Melanconidiaceae. ITS sequences of specimens from Alaska<br />

and Italy are identical. The basionym has been cited as Rehm:<br />

Ascomyceten 270 (1875) in ‘Index Fungorum’ reflecting an error<br />

in Saccardo (1882) but the correct number is Rehm: Ascomyceten<br />

280, which does not include a description.<br />

Donald M. Walker, Department of Natural Sciences, The University of Findlay, Findlay, OH 45840, USA; e-mail: walkerd@findlay.edu<br />

Amy Y. Rossman, Systematic Mycology & Microbiology Laboratory, USDA-ARS, Beltsville, MD 20705, USA; e-mail: Amy.Rossman@ars.usda.gov<br />

Gerard C. Adams, Department of Plant Pathology, University of Nebraska, Lincoln, NE 68583, USA; e-mail: gadams3@unl.edu<br />

Claudia Maria Oliveira Longa, FEM-IASMA - Research and Innovation Centre, Sustainable Agro-Ecosystems and Bioresources Department. Via E. Mach 1,<br />

38010 San Michele all’Adige (TN), Italy; e-mail: claudia.longa@fmach.it<br />

Giorgio Maresi, IASMA - Centre for Technology Transfer, Via E. Mach 1, 38010 San Michele all’Adige (TN), Italy; e-mail: giorgio.maresi@fmach.it<br />

© 2012 Nationaal Herbarium Nederland & Centraalbureau voor Schimmelcultures

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