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A new approach to species delimitation in Septoria - CBS - KNAW

A new approach to species delimitation in Septoria - CBS - KNAW

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A <strong>new</strong> <strong>approach</strong> <strong>to</strong> <strong>species</strong> <strong>delimitation</strong> <strong>in</strong> Sep<strong>to</strong>riaHosts: Paris quadrifolia, P. <strong>in</strong>completa and Viola palustris.Material exam<strong>in</strong>ed: Austria, Tirol, Leutaschtal Weidach, on river bank, on liv<strong>in</strong>gleaves of Paris quadrifolia, 2 Aug. 2000, G. Verkley 1038, <strong>CBS</strong> H-21177, liv<strong>in</strong>gcultures <strong>CBS</strong> 109110, 109111; Tirol, Ötztal, Sölden, near Hoch-Sölden, on liv<strong>in</strong>gleaves of Viola palustris, 31 July 2000, G. Verkley 1037, <strong>CBS</strong> H-21152, liv<strong>in</strong>gcultures <strong>CBS</strong> 109108, 109109.Notes: Accord<strong>in</strong>g <strong>to</strong> the orig<strong>in</strong>al description, conidia of S. paridisare 20 × 1 µm and aseptate. Vanev et al. (1997) describe theconidia as 18–25 × 1–1.3 µm, Teterevnikova-Babayan (1983),20–25 × 1 µm. As is seen <strong>in</strong> several other Sep<strong>to</strong>ria, the conidiacan reach considerably greater length <strong>in</strong> culture than on the naturalhost plant. In shape of the conidia the <strong>species</strong> strongly resemblesS. galeopsidis and S. scabiosicola, as do the cultures, although S.galeopsidis does not produce a red pigment on OA. The material onViola palustris (Violaceae) collected <strong>in</strong> Tirol was <strong>in</strong>itially identifiedas S. violae-palustris, but based on the DNA sequence analysesof seven loci (Fig. 2) and the agree<strong>in</strong>g phenotype it is concludedthat the material is conspecific with S. paridis. This is the first repor<strong>to</strong>f this fungus on another host genus than Paris, and also outsidethe Liliaceae. A second Sep<strong>to</strong>ria occurr<strong>in</strong>g on Paris quadrifolia isS. umbrosa. That <strong>species</strong> differs from S. paridis by much largerconidia, 30–85 × 3–4.5 µm, which are 5–7-septate.Sep<strong>to</strong>ria passifloricola Punith., CMI Descr. PathogenicFungi & Bacteria no. 670. 1980.≡ S. passiflorae Louw, Sci. Bull. Dept. Agric. For. Un. S. Africa 229: 34.1941. Nom. illeg. Art 53 [non Syd., Annls mycol. 37: 408. 1939].Description <strong>in</strong> vitro: Colonies on OA 12–15 mm diam <strong>in</strong> 2 wk, withan even, glabrous, buff marg<strong>in</strong>; colonies spread<strong>in</strong>g, immersedmycelium mostly homogeneous orange, but no diffusion ofpigments beyond the marg<strong>in</strong> observed; the surface covered byappressed, greyish white <strong>to</strong> grey aerial mycelium develop<strong>in</strong>g <strong>in</strong>concentric areas, beneath which mostly superficial, dark brown<strong>to</strong> almost black pycnidia or more complex conidiomata develop,releas<strong>in</strong>g pale whitish <strong>to</strong> dirty greyish droplets of conidial slime;reverse orange <strong>to</strong> sienna. Colonies on CMA 10–14 mm diam <strong>in</strong> 2wk, as on OA. Colonies on MEA 5–7(–10) mm diam <strong>in</strong> 2 wk, with aneven, weakly lobed, black marg<strong>in</strong>, which may be covered by shortfluffy, pure white aerial mycelium; colonies spread<strong>in</strong>g but elevatedat the centre, the surface almost black, with immersed conidiomatalcomplexes soon covered by masses of first pale white, buff, andthen brick conidial slime; the central area later entirely coveredby cerebriform, brick masses of slime; reverse brick <strong>to</strong> almostv<strong>in</strong>aceous, and fawn. Colonies on CHA 8–10(–14) mm diam <strong>in</strong>2 wk, with an even, buff marg<strong>in</strong> covered by a diffuse, felty aerialmycelium; further as on MEA, but surface less elevated, and largelycovered by diffuse, felty, grey-white aerial mycelium; conidialslime as on MEA abundantly produced from similar conidiomatalcomplexes, but more <strong>in</strong>tensely pigmented, deep scarlet; reverseblood colour.Conidiogenous cells (OA) hyal<strong>in</strong>e, discrete, broadlyampulliform <strong>to</strong> cyl<strong>in</strong>drical, holoblastic, with one or two <strong>in</strong>dist<strong>in</strong>ctpercurrent proliferations (sympodial proliferation not observed),8–14 × 3–6 µm; conidia filiform, hyal<strong>in</strong>e, narrowly rounded at the<strong>to</strong>p, attenuated <strong>to</strong> a truncate base, straight <strong>to</strong> somewhat curved,1–2(–3)-septate, not constricted around the septa, mostly 10–30(–35) × 1.5–2(–2.5) µm.Host: Passiflora edulis.Material exam<strong>in</strong>ed: Australia, Vic<strong>to</strong>ria, Wonthaggi, on Passiflora edulis, Mar. 2011,C. Murdoch, liv<strong>in</strong>g culture <strong>CBS</strong> 129431. New Zealand, Auckland, Mt Albert, onliv<strong>in</strong>g leaves of P. edulis, 21 Feb. 2000, C. F. Hill MAF LYN-118a, liv<strong>in</strong>g culture <strong>CBS</strong>102701.Notes: Priest (2006) provided a description of the fungus on thehost, and discussed the nomenclature. He also mentioned theanonymous report<strong>in</strong>g of a Sep<strong>to</strong>ria state observed <strong>in</strong> ascosporeisolates from a Mycosphaerella sp. found on fruits lesions, butwhether this truly is the sexual morph of S. passifloricola rema<strong>in</strong>s<strong>to</strong> be corroborated. The multilocus phylogeny (Fig. 2) providesevidence of a close relationship with S. ekmanniana (<strong>CBS</strong> 113385,113612) and S. chromolaenae (<strong>CBS</strong> 113373), and also S. sisyr<strong>in</strong>chii(<strong>CBS</strong> 112096) and S. anthurii (<strong>CBS</strong> 148.41, 346.58).Sep<strong>to</strong>ria petrosel<strong>in</strong>i (Lib.) Desm., Mem. Soc. Roy. Sci. Lille1843: 97. 1843. Fig. 32.Basionym: Ascochyta petrosel<strong>in</strong>i Lib., Pl. Crypt. Arduenna 3: 252.1834.≡ Phleospora petrosel<strong>in</strong>i (Lib.) Westend., Bull. Acad. r. Bruxelles 12 (9):252. 1845.Description <strong>in</strong> planta: Symp<strong>to</strong>ms leaf spots <strong>in</strong>def<strong>in</strong>ite, without adist<strong>in</strong>ct border, pale brown, visible on both sides <strong>in</strong> green partsof leaves or barely discoloured petioles. Conidiomata pycnidial,numerous, mostly epiphyllous, semi-immersed, black, mostly80–200 mm diam, with a central, first narrow, later wider open<strong>in</strong>g,releas<strong>in</strong>g pale white cirrhi of conidia; conidiomatal wall composedof one or two layers of brown-walled, angular cells, l<strong>in</strong>ed by alayer of hyal<strong>in</strong>e cells. Conidiogenous cells hyal<strong>in</strong>e, discrete,holoblastic, sympodially or percurrently proliferat<strong>in</strong>g, ampulliform,6–10 × 3–6 mm. Conidia hyal<strong>in</strong>e, filiform, straight <strong>to</strong> somewhatflexuous, the upper cell tapered <strong>in</strong><strong>to</strong> the obtuse apex, relativelywidely truncate at the base, (1–)3–5(–7) septate, not or only<strong>in</strong>dist<strong>in</strong>ctly constricted at the septa, contents granular or withm<strong>in</strong>ute oil-droplets around the septa and at the ends, 29–80 ×1.9–2.5 mm (liv<strong>in</strong>g; rehydrated, 1.2–1.5 mm wide). Sexual morphunknown.Description <strong>in</strong> vitro (18 °C, near UV) <strong>CBS</strong> 109521: Colonies onOA 13–16 mm diam <strong>in</strong> 2 wk, with an even, colourless marg<strong>in</strong>;colonies spread<strong>in</strong>g, immersed mycelium mostly pale ochreous,soon appear<strong>in</strong>g dull green due <strong>to</strong> the development of dark greenhyphal strands, particularly <strong>in</strong> a discont<strong>in</strong>uous submarg<strong>in</strong>alzone; reverse <strong>in</strong> the centre ochreous <strong>to</strong> fulvous, surrounded byolivaceous-grey. Conidiomata develop<strong>in</strong>g after 5–7 d immersed<strong>in</strong> the agar or on its surface, most numerous <strong>in</strong> the centre of thecolony, releas<strong>in</strong>g milky white <strong>to</strong> rosy-buff conidial slime. Conidiaalso produced directly from mycelium near the centre of thecolony. Colonies on MEA 17–20 mm diam <strong>in</strong> 2 wk, with an even<strong>to</strong> somewhat ruffled, buff marg<strong>in</strong>; colonies spread<strong>in</strong>g <strong>to</strong> restricted,somewhat elevated <strong>to</strong>wards the centre, the surface black withmany stromata develop<strong>in</strong>g and releas<strong>in</strong>g milky white droplets ofconidial slime, aerial mycelium diffuse <strong>to</strong> more dense and low,grey; reverse mostly greenish grey <strong>to</strong> iron-grey, <strong>in</strong> the centre withfawn <strong>to</strong> dark brick haze.Conidiomata and conidiogenous cells as <strong>in</strong> planta. Conidia(OA) filiform <strong>to</strong> filiform-cyl<strong>in</strong>drical, straight, flexuous or curved,attenuated gradually <strong>to</strong> the narrowly rounded <strong>to</strong> po<strong>in</strong>ted apex,attenuated gradually or more abruptly <strong>to</strong> the narrowly truncatebase, (0–)3–5(–7)-septate, 30–54(–65) × 2–2.5(–3) µm.www.studies<strong>in</strong>mycology.org277

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