4 μm, solitary, obclavate, straight, slightly curved, hyal<strong>in</strong>e, 6–12-septate, smooth, obconically truncate at the base, taper<strong>in</strong>g towards a subacute apex, hila 2–2.3 μm diam., conspicuous, thickened <strong>and</strong> darkened. Specimen exam<strong>in</strong>ed – THAILAND, Chiang Mai Prov<strong>in</strong>ce, Mae Jam District, Mae Hae Royal Project, on leaves of Conyza sumatrensis (Retz.) E. Walker (Asteraceae), 12 February 2008, Jamjan Meeboon <strong>and</strong> Iman Hidayat (BBH 23775). Hosts – Conyza ambigua, C. stricta, C. sumatrensis (Asteraceae) (Crous & Braun 2003, Meeboon 2009). Distribution – India, <strong>Thail<strong>and</strong></strong> (Crous & Braun 2003, Meeboon 2009). Notes – This specimen is much close to C. nilghirensis than to C. bidentis Tharp. due to dist<strong>in</strong>ct <strong>and</strong> amphigenous leaf spot, amphigenous caespituli, stromata small to lack<strong>in</strong>g, unbranched <strong>and</strong> geniculation of conidiophores near the apex, <strong>and</strong> the conidia frequently obclavate. In C. bidentis, the leaf spot is <strong>in</strong>def<strong>in</strong>ite as the lower surfaces <strong>and</strong> caespituli epiphyllous. The first report of C. nilghirensis from <strong>Thail<strong>and</strong></strong> was by Meeboon (2009). <strong>Cercospora</strong> z<strong>in</strong>niicola A. P<strong>and</strong>e, Kavaka 3: 55 (1975). Fig. 28–29 Leaf spots 1–10 mm diam., amphigenous, irregular, pale, <strong>with</strong> dark red marg<strong>in</strong>, numerous <strong>and</strong> scattered through the leaf surface. Caespituli amphigenous. Stromata 32.5–46 μm diam., <strong>in</strong>traepidermal, well-developed, composed of globose to subglobose, brown to blackish brown cells. Conidiophores 54–100 × 2.5–5 μm, 9–16 <strong>in</strong> dense fascicules, not divergent, 3–6-septate, aris<strong>in</strong>g from stromata, smooth, brown at the base, paler toward the apex, straight to decumbent, unbranched, cyl<strong>in</strong>drical, geniculate to s<strong>in</strong>uous, mostly near the apex. Conidiogenous cells 7.5–20 × 2.5–5 μm, <strong>in</strong>tegrated, term<strong>in</strong>al, holoblastic, mostly polyblastic, sympodially proliferat<strong>in</strong>g. Conidiogenous loci 2–2.5 μm diam., conspicuous, thickened <strong>and</strong> darkened. Conidia 24.5–93.5 × 2.5–3.5 μm, solitary, filiform to narrowly obclavate, straight, hyal<strong>in</strong>e, 7–18-septate, smooth, obconically truncate at the base, taper<strong>in</strong>g toward a subacute apex, hila 2–2.5 μm diam., thickened <strong>and</strong> darkened. 46 Specimens exam<strong>in</strong>ed – THAILAND, Chiang Rai Prov<strong>in</strong>ce, A. Wiang Pa Pao, T. Wiang Ga Long, Moo11, Bahn Tung Ruang Tong, on leaves of Z<strong>in</strong>nia elegans Jacq (Asteraceae), 31 July 2007, Jamjan Meeboon (BBH 23563); Chiang Mai Prov<strong>in</strong>ce, Mae Rim, Queen Sirikit Botanical Garden, on leaves of Z. elegans, 5 August 2008, Jamjan Meeboon, (BBH 23731). Hosts – Z<strong>in</strong>nia elegans (Asteraceae) (Crous & Braun 2003, Meeboon 2009). Distribution – India, <strong>Thail<strong>and</strong></strong> (Crous & Braun 2003, Meeboon 2009). Notes – Both of these specimens are apparently dist<strong>in</strong>ct from C. apii s. lat. due to well developed stromata, very densely fasciculate conidiophores <strong>and</strong> obclavate conidia <strong>with</strong> obconically truncate base. Both of them are characterized by hav<strong>in</strong>g amphigenous caespituli as well as hav<strong>in</strong>g relatively short conidiophores (up to 100 μm long) <strong>and</strong> conidia. The conidiophores of the first specimen are not divergent, but the second one is divergence <strong>and</strong> conidia of the second specimen are only up to 4 septate. S<strong>in</strong>ce these collections are not C. apii s. lat., therefore, we assigned them to C. z<strong>in</strong>niicola due to the similarity of morphological characteristics, <strong>and</strong> be<strong>in</strong>g recorded from Z<strong>in</strong>nia elegans. <strong>Cercospora</strong> z<strong>in</strong>niicola was firstly found <strong>in</strong> <strong>Thail<strong>and</strong></strong> by Meeboon (2009). Literature – Crous & Braun (2003, p. 434). <strong>Cercospora</strong> z<strong>in</strong>niae Ellis & G. Mart<strong>in</strong>, J. Mycol. 1: 20 (1885). = <strong>Cercospora</strong> atric<strong>in</strong>cta Heald & F.A. Wolf, Mycologia 3: 14 (1911). = <strong>Cercospora</strong> z<strong>in</strong>niae Takah. & Yosh., Pl. Protect. Tokyo 7: 17 (1953). (= C. apii s. lat.) Fig. 30 Leaf spots 15–30 mm diam., amphigenous, circular or subcircular, at first pale greenish to ochraceous, later brown to dark brown, f<strong>in</strong>ally <strong>with</strong> greyish brown centre, surrounded by a dark marg<strong>in</strong>s. Caespituli amphigenous, effuse. Stromata 17–25 μm diam., <strong>in</strong>traepidermal, small to well-developed, composed of globose to subglobose, brown to blackish brown cells. Conidiophores 40–152 × 3–5.5 μm, 9–13 <strong>in</strong> dense fascicles, often
Plant Pathology & Quarant<strong>in</strong>e Fig. 28 – L<strong>in</strong>e draw<strong>in</strong>gs of <strong>Cercospora</strong> z<strong>in</strong>niicola on Z<strong>in</strong>nia elegans. a. Conidia. b. Conidiophores <strong>and</strong> stroma. Bars = 50 µm. (Meeboon 2009). Fig. 29 – L<strong>in</strong>e draw<strong>in</strong>gs of <strong>Cercospora</strong> z<strong>in</strong>niicola on Z<strong>in</strong>nia elegans. a. Conidiophores <strong>and</strong> stromata. b. Conidia. Bars = 50 µm. (Meeboon 2009). 47
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