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Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014 [2015]

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Thelonectria pinea (Dingley) C. Salgado & P. Chaverri in Salgado-Salazar et al., Fungal Diversity 70 18 (2014 [2015])
Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014 [2015]

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Endemic
Present
New Zealand
Political Region

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(Dingley) C. Salgado & P. Chaverri
Dingley
C. Salgado & P. Chaverri
2014
2015
18
ICN
species
Thelonectria pinea

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Pinus radiata D. Don. Auckland, Whakarewarewa, September 1949; G. B. Rawlings.
Perithecia gregarious on a dark coloured, pulvinate prosenchy-matous stroma, globose 0-2-0.3mm. diameter, red, black when mature, ostiole papillate and surrounded by a distinct, often flattened zone 8-101, diameter; perithecial wall pseudoparenchymatous, 15-20 µm thick, cells 5-10,u diam., densely thickened and pigmented. Asci cylindrical sometimes clavate 75-100 x 6-10,u, 8 spored, obliquely uniseriate, bi-seriate at apex pseudoparaphyses filamentous. Spores one-septate, elliptical or oval 13-5-16 x 4-5-6µt, smooth, hyaline.
Europe, North America, New Zealand.
Pinus radiata.
Perithecia gregaria in stroinate fusco, pulverato, prosenchymato ; globosa, 0-2-0-3mm. diam., maturitate atrorubra; ostiolo papillato; pariete perithecii 15-201, crasso ; cellulis 5-10tt solide densatis et tinctis. Asci cylindrici interdum clavati 75-100 x 6-10[t; 8 sporis oblique uniseriatis, in apice biseriatis ; pseudoparaphysibus filamentous. Spores uniseptatae, ellipticae vel ovatae 13-5-16 x 4.5-6,u, leves, hyalinae.
There seems to have been some confusion in the literature as to the name of this species. Saccardo (1883) described sporidia within the immature ascus of N. cucurbitula and suggested that the species was synonymous with Chilonectria cucurbitula (Curr.) Sacc. and with Calonectria cucurbitula (Fr.) Sacc. Ellis and Everhart (1892) when recording N. cucurbitula stated that no sporidia were observed as described by Saccardo, while Seaver (1909) stated that the species Creonectria cucurbitula is not N. cucurbitula (Tode) Fr. but N. cucurbitula Sacc. Petch (7.938) noted that this species has been confused with N. coryli. N. cucurbitula (Tode) Fr. referred to two species of Nectria, one where sporidia were produced within the ascus i.e., N. coryli Fuckel (syn. Chilonectria cucurbitula (Curr.) Sacc.) and another species which Seaver described as Creonectria cucurbitula and Petch as Nectria cucurbitula Sacc. This is a case of `nomen eonfusum ' and the later species has been renamed and redescribed. As in N. tasinanica spores are smooth and hyaline, and perithecia are accompanied by tufts of hyaline mycelium but perithecia are smaller, thinner walled. Spores are elliptical and not as broad as the preceding species. As the species was found only on an introduced host, it seems probable that it has been introduced.
LOCALITY: Whakarewarewa, Rotorua.

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Nectria pinea Dingley 1951
Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014 [2015]
Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014 [2015]
Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014
Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014 [2015]

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New Zealand
Bay of Plenty
New Zealand
Coromandel
Thelonectria pinea (Dingley) C. Salgado & P. Chaverri 2014 [2015]
New Zealand
Bay of Plenty

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taxonomic status
Salgado et al. 2014 say: "Three species in the T. discophora complex occur in New Zealand, T. brayfordii, T. mammoidea and T. pinea. However T. pinea occurs only on P. radiata and has macroconidia 1–4-septate, and T. mammoidea is genetically highly divergent."

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780741c6-3c80-4b83-af8d-c720adffe74e
scientific name
Names_Fungi
21 February 2014
20 January 2015
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