Colletotrichum: complex species or species ... - CBS - KNAW
Colletotrichum: complex species or species ... - CBS - KNAW
Colletotrichum: complex species or species ... - CBS - KNAW
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Weir et al.<br />
of this <strong>species</strong> to C. psidii remains unknown. A new <strong>species</strong> on<br />
Psidium guajava, C. guajavae, belonging to the C. acutatum<br />
<strong>species</strong> <strong>complex</strong>, is described elsewhere in this volume (Damm<br />
et al. 2012a).<br />
Specimen examined: Italy, Rome, on Psidium sp., coll. M. Curzi (authentic culture<br />
of C. psidii – <strong>CBS</strong> 145.29 = ICMP 19120).<br />
Glomerella psidii (Delacr.) J. Sheld., Bull. West Virginia<br />
Agric. Exp. Sta. 104: 311. 1906.<br />
Basionym: Gloeosp<strong>or</strong>ium psidii Delacr., Bull. Soc. Mycol. France.<br />
19: 144. 1903.<br />
Notes: Sheldon (1906) produced perithecia in culture from<br />
isolates he considered typical of Gloeosp<strong>or</strong>ium psidii and on this<br />
basis recombined the <strong>species</strong> described by Delacroix (1903) in<br />
Glomerella. The relationship of G. psidii to <strong>Colletotrichum</strong> psidii,<br />
also described from guava, is not known. See notes under C. psidii.<br />
* <strong>Colletotrichum</strong> queenslandicum B. Weir & P.R. Johnst.,<br />
nom. nov. et stat. nov. MycoBank MB563593. Fig. 31.<br />
Basionym: <strong>Colletotrichum</strong> gloeosp<strong>or</strong>ioides var. minus Simmonds,<br />
Queensland J. Agric. Anim. Sci. 25: 178A. 1968. [as var. min<strong>or</strong>]<br />
Etymology: based on the region from which the type specimen of<br />
this <strong>species</strong> was collected.<br />
Holotype: Australia, Queensland, Ormiston, on Carica papaya, coll.<br />
J.H. Simmonds, Oct. 1965, IMI 117612.<br />
Epitype: Australia, Queensland, Brisbane, on Carica papaya, coll.<br />
J.H. Simmonds 11663C, Sep. 1965, epitype here designated PDD<br />
28797; ex-epitype culture ICMP 1778.<br />
Colonies grown from single conidia on Difco PDA 62–74 mm diam<br />
after 10 d, aerial mycelium either dense, cottony, unif<strong>or</strong>m, grey,<br />
<strong>or</strong> with aerial mycelium lacking, towards centre of colony with<br />
numerous, small acervuli with dark bases and <strong>or</strong>ange conidial<br />
ooze; in reverse cultures with copious aerial mycelium unif<strong>or</strong>mly<br />
dark grey (1F2), those with little aerial mycelium having a pinkish<br />
brown (8B4) pigment within the agar, the dark bases of the acervuli<br />
and the colour of the conidial ooze visible through the agar. Conidia<br />
(12–)14.5–16.5(–21.5) × (3.5–)4.5–5(–6) µm (av. 15.5 × 4.8 µm, n<br />
= 96), cylindric, straight, sometimes slightly constricted near centre,<br />
ends broadly rounded. Appress<strong>or</strong>ia about 6–12 µm diam., globose<br />
to sh<strong>or</strong>t-cylindric, rarely lobed. Perithecia not seen.<br />
Geographic distribution and host range: Known from Carica papaya<br />
and Persea americana from Queensland, Australia, and from<br />
Coffea berries from Fiji. Simmonds (1965) rep<strong>or</strong>ted from Australia<br />
what he considered to be the same fungus also from Mangifera<br />
indica, Malus sylvestris, and “many other hosts”.<br />
Genetic identification: ITS sequences do not separate C.<br />
queenslandicum from some C. fructicola, some C. siamense, and<br />
some C. tropicale isolates. It is best distinguished from these taxa<br />
using TUB2, GAPDH, <strong>or</strong> GS.<br />
Notes: The ex-type cultures cited by Simmonds (1968) are no<br />
longer in st<strong>or</strong>age at BRIP in Queensland (R. Shivas, pers. comm.)<br />
and presumably lost. However, we do have two cultures identified<br />
as C. gloeosp<strong>or</strong>ioides var. minus by Simmonds and isolated from<br />
the same host from the same locality as the holotype (Simmonds<br />
isolates 16633C and 1647A2), that had been sent to Joan Dingley<br />
in 1965 and subsequently st<strong>or</strong>ed in the ICMP culture collection.<br />
The culture selected here as epitype (Simmonds 11663C = ICMP<br />
1778) matches the Simmonds (1965) description of this fungus as<br />
having “an abundance of aerial mycelium in culture”. Our conidial<br />
measurements from ICMP 1778 and 1780 are broader than those<br />
given by Simmonds (1965), but he does note that “Confusion can<br />
occur between narrower strains of C. gloeosp<strong>or</strong>ioides and broader<br />
strains of C. gloeosp<strong>or</strong>ioides var. minus …”. Simmonds (1965) also<br />
notes that perithecia may rarely be seen in cultures of some isolates.<br />
The isolates accepted here as C. queenslandicum are<br />
genetically distinct within the Musae clade of C. gloeosp<strong>or</strong>ioides s.<br />
lat. <strong>Colletotrichum</strong> minus Zimm. (1901) requires that we propose a<br />
nom. nov. f<strong>or</strong> this fungus at <strong>species</strong> rank.<br />
Simmonds (1965) considered C. gloeosp<strong>or</strong>ioides var. minus<br />
to be the conidial state of Glomerella cingulata var. min<strong>or</strong><br />
Wollenw. Wollenweber & Hochapfel (1949) used the name<br />
Gloeosp<strong>or</strong>ium elasticae Cooke & Massee f<strong>or</strong> the conidial state<br />
of G. cingulata var. min<strong>or</strong>, the type specimens f<strong>or</strong> both names<br />
being from Ficus. Simmonds (1965) noted that it was not possible<br />
to transfer G. elasticae to <strong>Colletotrichum</strong> because <strong>Colletotrichum</strong><br />
elasticae had already been published f<strong>or</strong> a different fungus.<br />
However, rather than proposing a nom. nov. f<strong>or</strong> Gloeosp<strong>or</strong>ium<br />
elasticae, he described C. gloeosp<strong>or</strong>ioides var. minus as a new<br />
variety, with a different type specimen. Glomerella cingulata var.<br />
min<strong>or</strong> is genetically distinct from the specimen Simmonds chose<br />
as the type of C. gloeosp<strong>or</strong>ioides var. minus, see notes under G.<br />
cingulata var. min<strong>or</strong>.<br />
Other specimens examined: Australia, Queensland, Brisbane, on Carica sp.,<br />
coll. J.H. Simmonds 16347A2 (ICMP 1780, dried culture st<strong>or</strong>ed as PDD 28797);<br />
Queensland, Home Hill, on Persea americana, coll. L. Coates 22516, Feb. 1983<br />
(ICMP 12564). Fiji, on Coffea sp. berry, coll. R. Gounder, Apr. 1988 (ICMP 18705).<br />
Glomerella rufomaculans var. vaccinii Shear, Bull. T<strong>or</strong>rey<br />
Bot. Club. 34: 314. 1907.<br />
Notes: Placed here in synonymy with <strong>Colletotrichum</strong> kahawae<br />
subsp. ciggaro. See notes under C. kahawae subsp. ciggaro. Note<br />
that Saccardo & Trotter (1913) place Shear’s variety in Glomerella<br />
fructigena (Clint.) Sacc., a rarely used <strong>species</strong> name, placed in<br />
synonymy with G. cingulata by von Arx & Müller (1954).<br />
Specimen examined: USA, on Vaccinium macrocarpum leaves, coll. C.L. Shear,<br />
Apr. 1922 (authentic isolate of G. rufomaculans var. vaccinii – <strong>CBS</strong> 124.22 = ICMP<br />
19122).<br />
* <strong>Colletotrichum</strong> salsolae B. Weir & P.R. Johnst., sp. nov.<br />
MycoBank MB563589. Fig. 32.<br />
= <strong>Colletotrichum</strong> gloeosp<strong>or</strong>ioides “f. sp. salsolae” (Berner et al. 2009).<br />
Etymology: Based on C. gloeosp<strong>or</strong>ioides “f. sp. salsolae”, referring<br />
to the host from which this fungus was <strong>or</strong>iginally collected.<br />
Holotype: Hungary, on Salsola tragus, coll. D. Berner [specimen<br />
from plants inoculated with strain 96-067, <strong>or</strong>iginally collected I.<br />
Schwarczinger & L. Vajna on Salsola tragus from Bugac, near<br />
Kiskunsag National Park, 1996], BPI 878740; ex-holotype culture<br />
ICMP 19051.<br />
Colonies grown from single conidia on Difco PDA 38–42 mm diam<br />
after 10 d, aerial mycelium sparse, cottony, pale grey, surface of<br />
164