Abstract:In a randomized block factorial experiment, 1200 seedlings from four provenances, each of Pinus sylvestris, Pinus eontorta and Picea abies were inoculated with conidia (2 x lO'' and 1 x 10'' conidia/seedling) of Gremmeniella abietina {Bruncborstia pinea), isolated from P. eontorta plantations in northern Sweden. A further 600 seedlings were left as controls. The occurrence of symptoms and the extension of dead tissues on the annual shoots were recorded 13 months after inoculation. Only the higher spore dose re… Show more
“…However, infected P. contorta seedlings seemed more resistant in terms of survival rate, length of infected tissue, and recovery by production of new leaders. This is in accordance with earlier inoculation studies conducted in Britain (probably LTT) (Aitken 1993) and Sweden (STT) (Hansson 1998). In Hansson (1998), in situ inoculations caused significantly higher mortality and infection severity on P. sylvestris seedlings compared with P. contorta seedlings, even though the proportion of infected seedlings was equal between the two species.…”
Section: Discussionsupporting
confidence: 92%
“…This is in accordance with earlier inoculation studies conducted in Britain (probably LTT) (Aitken 1993) and Sweden (STT) (Hansson 1998). In Hansson (1998), in situ inoculations caused significantly higher mortality and infection severity on P. sylvestris seedlings compared with P. contorta seedlings, even though the proportion of infected seedlings was equal between the two species. The results in Hansson (1998) were surprising because field trials with pines 2-4 m in height (Hansson and Karlman 1997) and large-scale monitoring of pine plantations in northern Sweden with saplings 1-3 m in height (Karlman et al 1994) had found P. contorta to be more susceptible than P. sylvestris to STT G. abietina in terms of infection and mortality rates.…”
Section: Discussionsupporting
confidence: 92%
“…The results in Hansson (1998) were surprising because field trials with pines 2-4 m in height (Hansson and Karlman 1997) and large-scale monitoring of pine plantations in northern Sweden with saplings 1-3 m in height (Karlman et al 1994) had found P. contorta to be more susceptible than P. sylvestris to STT G. abietina in terms of infection and mortality rates. Hansson (1998) concluded that P. contorta and P. sylvestris may have the same ''genuine'' susceptibility to STT G. abietina, although the introduced P. contorta seem to be more affected by stress factors caused by extreme weather conditions.…”
To study the resistance of Pinus contorta Dougl. ex Loud. var. latifolia Engelm. ex Watts to large tree type (LTT) Gremmeniella abietina (Lagerberg) Morelet of the European race, seedlings of P. contorta and Pinus sylvestris L. were planted in gaps of an infected 40-year-old P. sylvestris stand in 2005 and assessed for symptoms in and 32% of the P. contorta and P. sylvestris seedlings were infected, respectively. However, mortality was lower and recovery was better in the P. contorta seedlings. The mean infection length on surviving seedlings was significantly shorter in P. contorta (4 cm) compared with P. sylvestris (10 cm), and 47% of the P. contorta seedlings had developed new leader shoots in 2007 compared with 19% of the P. sylvestris seedlings. Histopathological examinations of the transition zone of infected shoots showed that P. contorta, as well as P. sylvestris, produced ligno-suberized boundaries extending from healthy needle bases transversally across the shoots. Together with areas of phenol-filled cells, these boundaries completed the compartmentalization of the invaded outermost parts of a majority of the infected seedlings. Our results indicate that P. contorta is more resistant to LTT G. abietina than P. sylvestris.
Résumé: Afin d'étudier la résistance de Pinus contorta Dougl. ex Loud. var. latifolia Engelm. ex Watts au type grands arbres (TGA) de la race européenne de Gremmeniella abietina (Lagerberg) Morelet, des semis de P. contorta et de Pinus sylvestris L. furent plantés en 2005 dans des trouées à l'intérieur d'un peuplement infecté de P. sylvestris âgé de 40 ans. Les symptômes furent évalués en 2006-2007. En 2007, respectivement 45 % et 32 % des semis de P. contorta et de P.sylvestris furent infectés. Cependant, la mortalité était plus basse et la récupération meilleure chez les semis de P. contorta. La longueur moyenne des infections sur les semis survivants était significativement plus courte chez le P. contorta (4 cm) comparativement au P. sylvestris (10 cm), et 47 % des semis de P. contorta avaient développé de nouvelles pousses en 2007, comparativement à 19 % chez les semis de P. sylvestris. Des examens histopathologiques de la zone de transition des pousses infectées montrent que le P. contorta, comme le P. sylvestris, forment une barrière ligno-subéreuse s'étendant de la base des aiguilles saines transversalement à travers les pousses. Avec les cellules remplies de phénols, ces barrières complètent le compartimentage des parties envahies les plus distantes de la majorité des semis infectés. Nos ré-sultats indiquent que le P. contorta est plus résistant au TGA de G. abietina que le P. sylvestris.
“…However, infected P. contorta seedlings seemed more resistant in terms of survival rate, length of infected tissue, and recovery by production of new leaders. This is in accordance with earlier inoculation studies conducted in Britain (probably LTT) (Aitken 1993) and Sweden (STT) (Hansson 1998). In Hansson (1998), in situ inoculations caused significantly higher mortality and infection severity on P. sylvestris seedlings compared with P. contorta seedlings, even though the proportion of infected seedlings was equal between the two species.…”
Section: Discussionsupporting
confidence: 92%
“…This is in accordance with earlier inoculation studies conducted in Britain (probably LTT) (Aitken 1993) and Sweden (STT) (Hansson 1998). In Hansson (1998), in situ inoculations caused significantly higher mortality and infection severity on P. sylvestris seedlings compared with P. contorta seedlings, even though the proportion of infected seedlings was equal between the two species. The results in Hansson (1998) were surprising because field trials with pines 2-4 m in height (Hansson and Karlman 1997) and large-scale monitoring of pine plantations in northern Sweden with saplings 1-3 m in height (Karlman et al 1994) had found P. contorta to be more susceptible than P. sylvestris to STT G. abietina in terms of infection and mortality rates.…”
Section: Discussionsupporting
confidence: 92%
“…The results in Hansson (1998) were surprising because field trials with pines 2-4 m in height (Hansson and Karlman 1997) and large-scale monitoring of pine plantations in northern Sweden with saplings 1-3 m in height (Karlman et al 1994) had found P. contorta to be more susceptible than P. sylvestris to STT G. abietina in terms of infection and mortality rates. Hansson (1998) concluded that P. contorta and P. sylvestris may have the same ''genuine'' susceptibility to STT G. abietina, although the introduced P. contorta seem to be more affected by stress factors caused by extreme weather conditions.…”
To study the resistance of Pinus contorta Dougl. ex Loud. var. latifolia Engelm. ex Watts to large tree type (LTT) Gremmeniella abietina (Lagerberg) Morelet of the European race, seedlings of P. contorta and Pinus sylvestris L. were planted in gaps of an infected 40-year-old P. sylvestris stand in 2005 and assessed for symptoms in and 32% of the P. contorta and P. sylvestris seedlings were infected, respectively. However, mortality was lower and recovery was better in the P. contorta seedlings. The mean infection length on surviving seedlings was significantly shorter in P. contorta (4 cm) compared with P. sylvestris (10 cm), and 47% of the P. contorta seedlings had developed new leader shoots in 2007 compared with 19% of the P. sylvestris seedlings. Histopathological examinations of the transition zone of infected shoots showed that P. contorta, as well as P. sylvestris, produced ligno-suberized boundaries extending from healthy needle bases transversally across the shoots. Together with areas of phenol-filled cells, these boundaries completed the compartmentalization of the invaded outermost parts of a majority of the infected seedlings. Our results indicate that P. contorta is more resistant to LTT G. abietina than P. sylvestris.
Résumé: Afin d'étudier la résistance de Pinus contorta Dougl. ex Loud. var. latifolia Engelm. ex Watts au type grands arbres (TGA) de la race européenne de Gremmeniella abietina (Lagerberg) Morelet, des semis de P. contorta et de Pinus sylvestris L. furent plantés en 2005 dans des trouées à l'intérieur d'un peuplement infecté de P. sylvestris âgé de 40 ans. Les symptômes furent évalués en 2006-2007. En 2007, respectivement 45 % et 32 % des semis de P. contorta et de P.sylvestris furent infectés. Cependant, la mortalité était plus basse et la récupération meilleure chez les semis de P. contorta. La longueur moyenne des infections sur les semis survivants était significativement plus courte chez le P. contorta (4 cm) comparativement au P. sylvestris (10 cm), et 47 % des semis de P. contorta avaient développé de nouvelles pousses en 2007, comparativement à 19 % chez les semis de P. sylvestris. Des examens histopathologiques de la zone de transition des pousses infectées montrent que le P. contorta, comme le P. sylvestris, forment une barrière ligno-subéreuse s'étendant de la base des aiguilles saines transversalement à travers les pousses. Avec les cellules remplies de phénols, ces barrières complètent le compartimentage des parties envahies les plus distantes de la majorité des semis infectés. Nos ré-sultats indiquent que le P. contorta est plus résistant au TGA de G. abietina que le P. sylvestris.
“…Susceptibility of conifers to G. abietina is to some degree under genetic control of the host (Roll-Hansen, 1972;Nevalainen and Uotila, 1984;Stephan et al 1984;Dietrichson and Solheim, 1987;Aitken, 1993;Hansson 1998;Sonesson et al, 2007). However, the role of environmental factors in disease development is essential; severe epidemics occur exclusively under environmental conditions which both predispose the host and favour the spread and survival of the fungus (Donaubauer, 1972;Petäistö and Kurkela, 1993).…”
Gremmeniella abietina causes shoot dieback and stem cankers on conifers throughout Northern hemisphere. The aim of this study was to investigate the virulence of Turkish G. abietina isolates in a field experiment.The lower branches of 15-20-year-old P. nigra and C. libani in a plantation site at 1,050 m a.s.l. in Isparta were inoculated at 1-2-month intervals during September-January. Five isolates obtained from high altitude mountainous forests were used. Each isolate was inoculated into two branches per tree and repeated ten times on both tree species at each inoculation date. The branches were sampled at the end of February, and in August, and lesion lengths in the inner bark measured.The mean lesion length on P. nigra and C libani were 10.6 ± 0.8 and 3.8 ± 0.2 mm in February and 17.6 ± 1.4 and 7.8 ± 0.8 mm in August, respectively.Differences in the mean lesion length between the isolates were small. Nevertheless, there were significant differences between the isolates on P. nigra in November and January inoculations, and on C. libani at all four inoculation times.The mean lesion lengths for all isolates at both sampling dates was the highest (p < 0.01) in December inoculations for both P. nigra (22.0 ± 1.9 February; 32.9 ± 2.9 August) and C. libani (5.6 ± 0.7; 11.3 ± 1.2). There was no difference between the September and January inoculations on P. nigra, despite the almost six-fold difference in incubation period. During the December inoculations, the trees were most likely in winter dormancy, i.e. unable to defend themselves, which would explain the large lesions.
“…For other forest trees, considerable amount of research in this range was performed on elms in reference to Ophiostoma novo-ulmi Brasier (Santini et al 2005) and on pines and spruces towards Gremmeniella abietina (Lagerb.) M. Morelet (Roll-Hansen 1971;Hansson 1998), and also inter alia to Cenangium ferruginosum Fr. (Kuzmina, Kuzmin 2008).…”
Abstract. Phytophthora cambivora (Straminipila, Oomycota) causes root rot and stem canker on several deciduous tree species in Europe. However, very little is known about the variation in susceptibility to P. cambivora colonisation among provenances and families of pedunculate oak (Quercus robur L.). We studied variation in susceptibility of one French and 16 Polish provenances, representing 62 families. Samples were taken from three test plots located in the Brzesko Forest District. Oak susceptibility to P. cambivora was assessed by measuring lesion length following inoculation of excised shoots with two isolates of P. cambivora. There was significant variability in susceptibility among the 17 provenances tested. The highest susceptibility to P. cambivora was apparent in several provenances including Tronçais, Zaporowo, Runowo, Opole and Krotoszyn; while the most resistant provenances originated from Chojnów, Siedlce, Płock, Krotoszyn-90 and Wioska. There was also significant within-provenances variation in susceptibility to P. cambivora.
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