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 />
Group R:<br />
This group comprises five species that previously were accommodated<br />
<strong>in</strong> <strong>the</strong> sections Phoma, Peyronellaea and Phyllostictoides. As <strong>the</strong><br />
name <strong>of</strong> Ph. tropica already suggests, it concerns a <strong>the</strong>rmotolerant<br />
species, which is ma<strong>in</strong>ly found <strong>in</strong> European greenhouses on a wide<br />
range <strong>of</strong> hosts, but which probably has a tropical orig<strong>in</strong> (Schneider<br />
& Boerema 1975), as do most o<strong>the</strong>r species found <strong>in</strong> <strong>the</strong> present<br />
clade. The sole host <strong>of</strong> Ph. costarricensis is c<strong>of</strong>fee bean (C<strong>of</strong>fea<br />
arabica), while Ph. piperis is associated with Indian Long Pepper<br />
(Piper longus), and <strong>the</strong> novel species Ph. m<strong>in</strong>or has been isolated<br />
twice from clove (Syzygium aromaticum) <strong>in</strong> Indonesia. In addition,<br />
Ph. labilis is a warmth-preferr<strong>in</strong>g plurivorous species that has<br />
been isolated <strong>in</strong> European greenhouses and from nature <strong>in</strong> <strong>the</strong><br />
Middle East, Turkey and Indonesia (Boerema et al. 2004). Phoma<br />
zantedeschiae is widespread throughout <strong>the</strong> Western Hemisphere,<br />
but always <strong>in</strong> association with arum or calla (Zantedeschia sp.), a<br />
genus that is <strong>in</strong>digenous <strong>in</strong> sou<strong>the</strong>rn Africa (Boerema & Hamers<br />
1990). Thus far, however, no data <strong>of</strong> temperature-growth studies<br />
are available for <strong>the</strong>se species except for Ph. tropica. Several o<strong>the</strong>r<br />
<strong>the</strong>rmotolerant species, such as Ph. calidophila, Ph. calorpreferens<br />
and Ph. multirostrata, are, however, not accommodated <strong>in</strong> this group.<br />
These three species are soil-borne, <strong>in</strong> contrast to Ph. tropica and Ph.<br />
costarricensis, which are associated with leaf-spots.<br />
Phoma tropica and Ph. costarricensis are both closely related,<br />
and colony characters are highly similar. However, <strong>the</strong> stra<strong>in</strong>s<br />
available revealed a significant difference <strong>in</strong> conidial and pycnidial<br />
sizes, consistent with <strong>the</strong> data obta<strong>in</strong>ed <strong>in</strong> previous studies<br />
(Schneider & Boerema 1975, De Gruyter & Noordeloos 1992).<br />
Phoma costarricencis Echandi, Rev. Biol. Trop. 5: 83. 1957.<br />
Specimens exam<strong>in</strong>ed: Nicaragua, from a twig <strong>of</strong> C<strong>of</strong>fea sp., 1991, CBS 506.91 =<br />
PD 91/876 = IMI 215229. Unknown orig<strong>in</strong>, from C<strong>of</strong>fea arabica, 1979, CBS 497.91<br />
= PD 79/209.<br />
Notes: Stra<strong>in</strong> CBS 497.91 was <strong>in</strong>itially identified as Ph. tropica.<br />
The close phylogenetic association between this species and<br />
Ph. costarricensis concurs with <strong>the</strong>ir overlapp<strong>in</strong>g morphological<br />
characters (see Schneider & Boerema 1975, De Gruyter &<br />
Noordeloos 1992).<br />
Phoma labilis Sacc., Michelia 2(7): 341. 1881.<br />
Specimens exam<strong>in</strong>ed: Israel, from a stem <strong>of</strong> Rosa sp., 1970, G.H. Boerema, CBS<br />
479.93 = PD 70/93. The Ne<strong>the</strong>rlands, Barendrecht, from a stem <strong>of</strong> Lycopersicon<br />
esculentum, 1987, J. de Gruyter, CBS 124.93 = PD 87/269.<br />
Phoma m<strong>in</strong>or Aveskamp, Gruyter & Verkley, sp. nov.<br />
MycoBank MB515641. Fig. 11.<br />
Conidia ellipsoidea, ovoidea vel leniter allantoidea, glabra, hyal<strong>in</strong>a, cont<strong>in</strong>ua,<br />
(3–)3.5–4.5(–5) × 1.8–2.5(–3) μm, (0–)1–3(–4) guttulis m<strong>in</strong>utis praedita. Matrix<br />
conidiorum alba.<br />
Etymology: Epi<strong>the</strong>t derived from <strong>the</strong> small-sized conidia.<br />
Conidiomata pycnidial, solitary, (sub-)globose to broadly ellipsoidal,<br />
glabrous or with some hyphal outgrows, on <strong>the</strong> agar surface and<br />
immersed, (125–)150–280(–330) × (125–)150–220(–245) μm.<br />
Ostioles (1–5), slightly papillate or non-papillate. Pycnidial wall<br />
pseudoparenchymatous, composed <strong>of</strong> oblong to isodiametric<br />
cells, outer cell layer pigmented, 2–4 layers, 8–15 μm thick.<br />
Conidiogenous cells phialidic, hyal<strong>in</strong>e, simple, smooth, flaskshaped<br />
or somewhat isodiametric, ca. 4–5.5(–6.2) × 3–4.5(–4.7)<br />
42<br />
μm. Conidia ellipsoidal to ovoid or slightly allantoid, th<strong>in</strong>-walled,<br />
smooth, hyal<strong>in</strong>e, aseptate (3–)3.5–4.5(–5) × 1.8–2.5(–3) μm, with<br />
(0–)1–3(–4) m<strong>in</strong>ute guttules. Conidial matrix white.<br />
Culture characteristics: Colonies on OA (44–)45–50(–54) mm<br />
diam after 7 d, marg<strong>in</strong> regular. Aerial mycelium flat, grey, but<br />
locally well-developed <strong>in</strong> densely floccose white tufts. Immersed<br />
mycelium olivaceous with rosy-buff t<strong>in</strong>ges near <strong>the</strong> colony marg<strong>in</strong>;<br />
reverse concolourous. Colonies on MEA 46-48 mm diam after 7 d,<br />
marg<strong>in</strong> regular. Immersed mycelium hyal<strong>in</strong>e, with abundant semiimmersed<br />
pycnidia, but almost completely covered by an aerial<br />
mycelial mat. Aerial mycelium pluriform, with a compact white mat<br />
and some felty glaucous grey or dull green zones, near colony<br />
marg<strong>in</strong> white; reverse black to grey-olivaceous. Colonies on CHA<br />
50–54 mm diam. after 7 d, marg<strong>in</strong> regular. Aerial mycelium similar<br />
as on MEA, although <strong>the</strong> felty white and glaucous grey zones are<br />
less abundant; reverse slate blue to leaden-black. Application <strong>of</strong><br />
NaOH results <strong>in</strong> a greenish yellow discolouration <strong>of</strong> <strong>the</strong> agar, best<br />
to be observed on OA medium.<br />
Specimens exam<strong>in</strong>ed: Indonesia, Sumatra, from Syzygium aromaticum, Apr. 1982,<br />
R. Kasim, holotype designated here CBS H-20236, ex-holotype culture CBS<br />
325.82; Lampung, from Syzygium aromaticum, Dec. 1982, H. Vermeulen, CBS<br />
315.83.<br />
Notes: As for Ph. eucalyptica, this species has been recorded <strong>in</strong><br />
association with clove trees (Syzygium aromaticum, Boerema et<br />
al. 2004). Both species, although genetically dist<strong>in</strong>ct, have many<br />
characters <strong>in</strong> common, notably <strong>the</strong> colony characters on OA, <strong>the</strong><br />
high variation <strong>in</strong> ostiole number and a similar reaction to application<br />
<strong>of</strong> NaOH. Although Phoma m<strong>in</strong>or produces relatively small conidia,<br />
<strong>the</strong> conidia <strong>of</strong> Ph. eucalyptica are even smaller, measur<strong>in</strong>g only 2–4<br />
× 1–2 μm (De Gruyter & Noordeloos 1992).<br />
Phoma piperis (Tassi) Aa & Boerema, Persoonia 15(3): 398.<br />
1993.<br />
Basionym: Phyllosticta piperis Tassi, Boll. Reale Orto Bot. Siena<br />
3(2): 28. 1900.<br />
Specimens exam<strong>in</strong>ed: The Ne<strong>the</strong>rlands, Tiel, from a leaf <strong>of</strong> Peperomia pereskiifolia,<br />
1988, J. de Gruyter, CBS 268.93 = CBS 108.93 = PD 88/720; Tiel, from Peperomia<br />
sp., 1990, J. de Gruyter, PD 90/2011<br />
Phoma tropica R. Schneid. & Boerema, Phytopathol. Z. 83<br />
(4): 361. 1975.<br />
Specimen exam<strong>in</strong>ed: Germany, Horrheim, from Sa<strong>in</strong>tpaulia ionantha, 1973, R.<br />
Schneider, isotype CBS H-7629, ex-isotype culture CBS 436.75.<br />
Phoma zantedeschiae Dippen., S. African J. Sci. 28: 284.<br />
1931.<br />
Specimen exam<strong>in</strong>ed: The Ne<strong>the</strong>rlands, from a bulb <strong>of</strong> Zantedeschiae sp., 1969,<br />
G.H. Boerema, CBS 131.93 = PD 69/140.<br />
Group S – Stagonosporopsis:<br />
This large group (BPP = 1.00, RBS = 55 %) comprises ma<strong>in</strong>ly<br />
species with Stagonosporopsis synanamorphs. In <strong>the</strong> Boeremaean<br />
classification system, <strong>the</strong>se species were embedded <strong>in</strong> Phoma<br />
section Heterospora (Boerema et al. 1997). As with <strong>the</strong> o<strong>the</strong>r<br />
sections, this group also appeared to be artificial. Based on LSU<br />
and SSU sequences, <strong>the</strong> type species <strong>of</strong> <strong>the</strong> section Heterospora,<br />
Ph. heteromorphospora, clusters outside <strong>the</strong> <strong>Didymellaceae</strong> (De<br />
Gruyter et al. 2009), as do Ph. samarorum and Ph. dimorphospora.