A Gremmeniella abietina (Lagerb.) race of type A was found to produce pycnidia in cankers of previous year’s shoots (1991) on branches of Scots pine (Pinus sylvestris L.) bearing green needles and living buds in the current-year shoots (1992) with no apparent symptoms of infection by G. abietina. The restricted colonization of green shoots by G. abietina, with only restricted canker development, may indicate that older, slow-growing natural Scots pines of the northern boreal forests resists the fungus well. However, the ability of the fungus to survive and even sporulate in such cankers indicates one way of surviving over consecutive years otherwise unfavourable for it.
Damage on Scots pine (Pinus sylvestris L.) caused by Gremmeniella abietina (Lagerb.) Morelet was assessed in the summer of 1992 in 67 stands in eastern Lapland. The area and severity of damage were smaller and lighter than had earlier been estimated and occurred especially in stands in the first-thinning stage or in middle-age. Significant new infection of 1991 occurred in stands previously heavily infected by G. abietina near Kemihaara river, lake Naruska, the Naruska river, the Tuntsa river and lake Vilma. Fresh damage occurred mainly in the lower or middle parts of the Scots pine canopies.
Ascocalyx abietina (now Gremmeniella abietina Lagerb.) infects Scots pine (Pinus sylvestris L.) by means of ascospores or conidia. Ascospores are dispersed by the wind, while the conidia are splash dispersed. The infection rate is positively correlated with the number of inocula. The aim of this study was to determine the extent to which G. abietina spreads to the trees surrounding the diseased trees and to find the correct time to perform sanitation cutting.
The results were obtained from Ascocalyx-inventory carried out in a Scots pine progeny test at Loppi, Southern Finland. Three Siberian provenances were totally destroyed, while the Finnish progenies remained relatively healthy. The two rows adjacent to the destroyed plots were inventoried separately.
There were 29.7% more diseased or dead trees in the two adjacent rows than in the rest of the same plots. The difference was statistically significant. The trees had probably been infected by conidia, because the effect of the destroyed plot only extended to the adjacent two rows. Furthermore, pycnidia had mainly developed on the dead shoots.
On the basis of the life cycle of the fungus and the results, the correct time to carry out sanitation cutting is the first winter after the disease symptoms have appeared. If it is done later, the disease could be spread and bark beetles (Tomicus spp.) could propagate in dying trees. Susceptible provenances may spread the disease to surrounding resistant trees owing to the increasing number of spores.
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Mineral soil sites where Scots pine (Pinus sylvestris L.) were suffering from Gremmeniella abietina die-back (Lagerb.) M. Morelet. were characterized and classified in Central Finland. The tree stand, ground vegetation, soil type and site topography were described in 163 sample plots in 16 stands. The sites were classified according to system developed by Cajander and numerically using TWINSPAN analysis based on the ground vegetation. The site topography of severely damaged stands was checked from colour infrared aerial photographs. The disease was most severe in depressions and frost pockets. Apart from topography no significant correlations were found between disease severity and site factors. No typical vegetational pattern of forest type of the severely affected stands could be detected. Most of the stands were growing on medium-coarse, unfertile soil with a rather thick humus layer.
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