2001
DOI: 10.1139/b01-090
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Relative abundance and potential dispersal range of intersterility groups of Heterobasidion annosum in pure and mixed forests

Abstract: In Europe the forest pathogen Heterobasidion annosum (Fr.) Bref. includes the S, P, and F intersterility groups (ISGs), each displaying a preferential specialization on Norway spruce (Picea abies (L.) Karst.), pine, and silver fir (Abies alba Mill.), respectively. In this paper, we present data about (i) H. annosum ISGs frequency in different forest types, (ii) the degree of host specificity of each ISG, (iii) the significance of the potential movement of airborne spores among forests, and (iv) the occurrence … Show more

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Cited by 48 publications
(68 citation statements)
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“…From several Heterobasidion isolates collected in the Lazio region (central Italy) and already screened for identification by mitochondrial DNA analysis (Gonthier et al 2001), five H. annosum and five H. irregulare heterokaryons were chosen for a growth test on agar medium and for an inoculation test on pine seedlings (Table 1). They were also characterized by sequence analyses of the nucleic gene of the elongation factor 1-α and the mitochondrial gene of the ATP synthase subunit 6 (Johannesson and Stenlid 2003;Kretzer and Bruns 1999).…”
Section: Isolatesmentioning
confidence: 99%
“…From several Heterobasidion isolates collected in the Lazio region (central Italy) and already screened for identification by mitochondrial DNA analysis (Gonthier et al 2001), five H. annosum and five H. irregulare heterokaryons were chosen for a growth test on agar medium and for an inoculation test on pine seedlings (Table 1). They were also characterized by sequence analyses of the nucleic gene of the elongation factor 1-α and the mitochondrial gene of the ATP synthase subunit 6 (Johannesson and Stenlid 2003;Kretzer and Bruns 1999).…”
Section: Isolatesmentioning
confidence: 99%
“…After 3 weeks, a small piece of mycelium was taken from the side of each of the two isolates and transferred into a new petri dish, resulting in hybrids with identical nuclear genomes but one with a mitochondrial genome of H. abietinum and the other with a mitochondrial genome of H. parviporum. The hybrid nature of the isolates was revealed by the presence of clamp connections in the mycelia, and mitochondrial characterization was done using a taxon-specific competitive-priming PCR technique as previously described (21). Inoculum and inoculation techniques were as described for experiment one.…”
Section: Inoculation Studies (I) Experiments Onementioning
confidence: 99%
“…Bref. Samples were incubated for at least 10 days in moist conditions at about 24°C and examined for the presence of the pathogen by using a dissecting microscope (ϫ20 magnification), as described by Gonthier et al (2001).…”
Section: Phytosanitary Surveys and Analysesmentioning
confidence: 99%