Highlights of the Didymellaceae - Studies in Mycology
Highlights of the Didymellaceae - Studies in Mycology
Highlights of the Didymellaceae - Studies in Mycology
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AveSkAMp et al.<br />
Fig. 12. Conidial dimorphism <strong>in</strong> three species <strong>of</strong> Stagonosporopsis. A. S. actaeae (CBS 106.96). B. S. lup<strong>in</strong>i (CBS 101494). C. S. cucurbitacearum (CBS 109171). Scale bars:<br />
A = 20 μm; B–C = 10 μm.<br />
subboltshauseri appears to occur worldwide on Fabaceae.<br />
However, Boerema et al. (2004) suggested that <strong>the</strong> orig<strong>in</strong>al host<br />
<strong>of</strong> this species may have been Phaseolus, which is native to <strong>the</strong><br />
Americas.<br />
A fourth and fifth (S4, S5) subclade <strong>in</strong> this group comprise species<br />
that are accommodated <strong>in</strong> section Phoma, and <strong>the</strong>refore lack any<br />
fur<strong>the</strong>r features than a pla<strong>in</strong>, globose pycnidium and aseptate,<br />
hyal<strong>in</strong>e conidia. The species found here are Ph. dorenboschiae,<br />
Ph. loticola (both S4), Ph. ajacis and Ph. valerianellae (both S5).<br />
In group S several taxa have been found with a teleomorph<br />
<strong>in</strong> Didymella, such as Ph. ligulicola var. ligulicola (teleomorph D.<br />
ligulicola var. ligulicola), Ph. ligulicola var. <strong>in</strong>oxydabilis (D. ligulicola<br />
var. <strong>in</strong>oxydabilis), and Ph. cucurbitacearum (D. bryoniae). Also <strong>the</strong><br />
teleomorph <strong>of</strong> Ph. caricae-papayae has been recovered <strong>in</strong> this<br />
study, and found to be a Didymella, which is <strong>in</strong> l<strong>in</strong>e with <strong>the</strong> o<strong>the</strong>r<br />
teleomorph observations <strong>in</strong> this clade. The current teleomorph<br />
state <strong>of</strong> this species is accommodated <strong>in</strong> Mycosphaerella as M.<br />
caricae (Sivanesan 1990).<br />
As <strong>the</strong> species <strong>in</strong> <strong>the</strong> present clade form a well-def<strong>in</strong>ed group<br />
with<strong>in</strong> <strong>the</strong> <strong>Didymellaceae</strong>, <strong>the</strong> taxa are recomb<strong>in</strong>ed <strong>in</strong>to <strong>the</strong> genus<br />
Stagonosporopsis. This fur<strong>the</strong>r implies that <strong>the</strong> names <strong>of</strong> <strong>the</strong><br />
Stagonosporopsis synanamorphs <strong>of</strong> Ph. samarorum and Ph.<br />
narcissi (S. frax<strong>in</strong>i and S. curtisii respectively) should no longer be<br />
used.<br />
Stagonosporopsis Died., Ann. Mycol. 10(2): 142. 1912.<br />
emend. Aveskamp, Gruyter & Verkley. Fig. 12.<br />
Conidiomata pycnidial, globose to subglobose, measur<strong>in</strong>g 70–300<br />
μm diam, on agar surface or immersed, solitary or confluent,<br />
ostiolate or poroid. Pycnidial wall pseudoparenchymatous, count<strong>in</strong>g<br />
2–6 cell layers <strong>of</strong> which <strong>the</strong> outer 1–3 are brown/olivaceous<br />
pigmented. Conidiogenous cells phialidic, hyal<strong>in</strong>e, simple, smooth,<br />
ampulliform or doliiform, ca. 4–7.5 × 3–6 µm. Conidia <strong>of</strong>ten <strong>in</strong><br />
two types: majority aseptate, hyal<strong>in</strong>e, ellipsoidal to subglobose,<br />
th<strong>in</strong>-walled, smooth, measur<strong>in</strong>g (3–)3.5–10 × 1.5–3(–3.5) μm.<br />
Conidia <strong>of</strong> <strong>the</strong> second type can be produced both <strong>in</strong> vivo and <strong>in</strong><br />
vitro <strong>in</strong> <strong>the</strong> same pycnidia as <strong>the</strong> smaller spores, unicellular or<br />
with up to 3 septa, measur<strong>in</strong>g up to 30 × 8 μm. Pseudo<strong>the</strong>cia, if<br />
present, occurr<strong>in</strong>g only <strong>in</strong> vivo, globose to subglobose, sometimes<br />
with a somewhat conical neck, measur<strong>in</strong>g 90–230 μm diam. Asci<br />
cyl<strong>in</strong>drical or subclavate, measur<strong>in</strong>g 50–90 × 9–13 µm, always<br />
8-spored, biseriate. Ascospores ellipsoid, fusiform or obovoid,<br />
measur<strong>in</strong>g 12–18 × 4–7 µm, uniseptate, guttulate.<br />
44<br />
Stagonosporopsis actaeae (Allesch.) Died., Ann. Mycol.<br />
10: 141. 1912.<br />
Basionym: Act<strong>in</strong>onema actaeae Allesch., Ber. bayer. bot. Ges. 5:<br />
7. 1897.<br />
= Phoma actaeae Boerema, Gruyter & Noordeloos, Persoonia 16(3): 347.<br />
1997.<br />
Specimens exam<strong>in</strong>ed: The Ne<strong>the</strong>rlands, Zeist, from a stem <strong>of</strong> Cimicifuga simplex,<br />
1974, G.H. Boerema, CBS 105.96 = PD 74/230; Limburg, Schaersbergerbos, from<br />
a leaf <strong>of</strong> Actaea spicata, 1994, J. de Gruyter, L 992.167.501, culture CBS 106.96<br />
= PD 94/1318.<br />
Notes: In contrast to <strong>the</strong> earlier description <strong>of</strong> <strong>the</strong> Phoma anamorph<br />
<strong>of</strong> this species (Boerema et al. 1997), <strong>the</strong> larger conidia regularly<br />
produces up to 3-septate conidia (see Fig. 12A). In <strong>the</strong> study<br />
mentioned above and <strong>in</strong> <strong>the</strong> present one <strong>the</strong> same stra<strong>in</strong>s were<br />
exam<strong>in</strong>ed morphologically.<br />
Stagonosporopsis ajacis (Thüm.) Aveskamp, Gruyter<br />
& Verkley, comb. nov. MycoBank MB515653.<br />
Basionym: Phyllosticta ajacis Thüm., apud Bolle & von Thümen,<br />
Boll. Soc. Adriat. Sci. Nat. Trieste 6: 329. 1880.<br />
= Phoma ajacis Aa & Boerema, apud De Gruyter, Noordeloos & Boerema,<br />
Persoonia 15(3): 383. 1993.<br />
Specimens exam<strong>in</strong>ed: Kenya, from Delph<strong>in</strong>ium sp., 1990, Hopman, L 993.034.225,<br />
culture CBS 177.93 = PD 90/115. The Ne<strong>the</strong>rlands, Ter Aar, from Delph<strong>in</strong>ium sp.,<br />
1986, CBS 176.93 = PD 86/547.<br />
Stagonosporopsis andigena (Turkenst.) Aveskamp,<br />
Gruyter & Verkley, comb. nov. MycoBank MB515655.<br />
Basionym: Phoma andigena Turkenst., apud Boerema, Gruyter &<br />
Noordeloos, Persoonia 16(1): 131. 1995.<br />
Specimens exam<strong>in</strong>ed: Peru, Dep. Jun<strong>in</strong>, Huancayo, near Vallis Mantaro, from a leaf<br />
<strong>of</strong> Solanum sp., 1975, L.J. Turkensteen, CBS 101.80 = PD 75/909 = IMI 386090;<br />
Dep. Jun<strong>in</strong>, Huancayo, near Vallis Mantaro, from a leaf <strong>of</strong> Solanum sp., 1975, L.J.<br />
Turkensteen, CBS 269.80 = PD 75/914.<br />
Stagonosporopsis artemisiicola (Hollós) Aveskamp,<br />
Gruyter & Verkley, comb. nov. MycoBank MB515656.<br />
Basionym: Phoma artemisiicola Hollós, Mat. Természettud.<br />
Közlem. 35: 40. 1926. (as "artemisaecola")<br />
Specimen exam<strong>in</strong>ed: France, from a stem base <strong>of</strong> Artemisia dracunculus, 1973,<br />
CBS 102636 = PD 73/1409.