Spruce Budworm Damage in Aspen/Balsam Fir Stands Affected by Cutting Methods

1987 ◽  
Vol 4 (2) ◽  
pp. 73-75 ◽  
Author(s):  
Harold O. Batzer ◽  
John W. Benzie ◽  
Michael P. Popp

Abstract An aspen/balsam fir study area in Wisconsin with several replicated cutting treatments dating from 1950 when the stand was 36 years old became infested by the spruce budworm in 1976. Remeasurement in 1981 revealed that balsam fir mortality and growth loss were directly related to the amount of aspen removed from the overstory. Complete and commercial clearcutting of the overstory aspen produced 60% more balsam fir basal area than uncut plots by 1975. However, mortality from budworm defoliation averaged 98% of the basal area in these plots. Thinning from above best achieved the objective of early release and provided near maximum protection from the spruce budworm. North. J. Appl. For. 4:73-75, June 1987.

1996 ◽  
Vol 13 (2) ◽  
pp. 73-78 ◽  
Author(s):  
Harald Piene ◽  
Janine D'Amours ◽  
Alan A. Bray

Abstract Comparisons of estimates of volume and volume increment, based on increment cores sampled at breast height and on stem analysis, were made in a young balsam fir stand that had been defoliated by spruce budworm. Use of increment cores is not recommended to estimate individual tree growth, because large errors, ranging from 20.9 to 57.2%, and error variability can be expected. The inability, when using increment cores, to estimate basal area is the major source of this variation. Although large uncertainties are associated with future growth predictions, on a per ha basis, changes over time based on increment cores may in some instances give comparable results to those based on stem analysis due to the canceling effect of trees being approximately equally overestimated and underestimated. However, a prerequisite is that the defoliation history and the year of individual tree death are known in detail to aid in the correct dating of ring widths. North. J. Appl. For. 13(2):73-78.


1964 ◽  
Vol 40 (3) ◽  
pp. 372-383 ◽  
Author(s):  
R. J. Hatcher

A study was made of the effect of the 1945-1957 spruce budworm infestation on 1,800 acres of spruce-fir and spruce-fir-hardwood forest logged for pulpwood about 15 years prior to the infestation.The number of fir trees was reduced 64 per cent between 1951 and 1961 in the main cover type representing 69 per cent of the forest; fir was reduced from a major stand component of 45 per cent by volume to a minor component of 11 per cent. The basal area reduction of fir varied directly with the fir basal area at the time of the outbreak. Losses were very high in stands containing over 20 sq. ft. of fir per acre.These young stands did not exhibit the degree of resistance to damage often observed in young stands elsewhere. But in spite of heavy losses through all diameter classes, the amount of spruce and fir regeneration that survived to 1961 is believed adequate to produce a pulpwood crop within 60 years.


1998 ◽  
Vol 28 (5) ◽  
pp. 703-710 ◽  
Author(s):  
Erhard John Dobesberger

A stochastic simulation model was developed to derive a damage function for the spruce budworm, Choristoneura fumiferana Clem. (Lepidoptera: Tortricidae), and balsam fir, Abies balsamea (L.) Mill., herbivore interaction at the stand level for open-grown trees. Both aggregated and uniform models of attack pattern by late-instar larvae based on k of the negative binomial were evaluated to determine the impact of larval density and attack pattern on the loss in stemwood volume increment of young, thinned balsam fir stands in Newfoundland. Percentage loss in stemwood increment was a nonlinear, negative exponential function of initial larval density. Implementation of control measures to prevent 50% defoliation that is caused by about 14 larvae/branch tip would result in saving 24% of the annual stemwood increment after 1 year of defoliation and about 32% after 2 years of cumulative defoliation. Aggregation of spruce budworm larvae among trees within a forest stand results in less growth loss compared with a uniform pattern of attack. The nonlinear damage function may suggest tolerance and possibly compensatory growth after herbivory by low population levels of the spruce budworm.


1996 ◽  
Vol 72 (4) ◽  
pp. 393-398 ◽  
Author(s):  
Éric Bauce

Field rearing experiments of spruce budworm, Choristoneura fumiferana (Clem.), were conducted in conjunction with foliar chemical analyses, one and two years after a commercial thinning (removal of 25% stand basal area) in a 50-year-old balsam fir, Abies balsamea (L.) Mill., stand. The first year after thinning, spruce budworm larvae reared on the residual trees developed five days faster and removed 43% more foliage than those reared on control trees, but in the second year they developed two days faster and removed 37% more foliage. The increase in larval development rate was related to an increase in foliar soluble sugars while a reduction in foliar monoterpenes caused by the thinning apparently accounted for the greater amount of foliage ingested by the larvae. The first year after thinning, trees were more vulnerable to spruce budworm because there was no increase in foliage production and the trees were more heavily defoliated. However, in the second year trees were less vulnerable to the insect because there was an increase in foliage production that exceeded the increase in defoliation, hence a net gain in foliage. Results from this study showed that commercial thinning could reduce the vulnerability of balsam fir trees to spruce budworm if thinning is conducted two years prior to budworm outbreak, but the same silvicultural procedure could increase the vulnerability to the insect if it is conducted during an outbreak. Key words: spruce budworm, balsam fir, chemistry, thinning, defoliation


Forests ◽  
2019 ◽  
Vol 10 (3) ◽  
pp. 232 ◽  
Author(s):  
Mingke Li ◽  
David MacLean ◽  
Chris Hennigar ◽  
Jae Ogilvie

We investigated the spatial-temporal patterns of spruce budworm (Choristoneura fumiferana (Clem.); SBW) defoliation within 57 plots over 5 years during the current SBW outbreak in Québec. Although spatial-temporal variability of SBW defoliation has been studied at several scales, the spatial dependence between individual defoliated trees within a plot has not been quantified, and effects of defoliation level of neighboring trees have not been addressed. We used spatial autocorrelation analyses to determine patterns of defoliation of trees (clustered, dispersed, or random) for plots and for individual trees. From 28% to 47% of plots had significantly clustered defoliation during the 5 years. Plots with clustered defoliation generally had higher mean defoliation per plot and higher deviation of defoliation. At the individual-tree-level, we determined ‘hot spot trees’ (highly defoliated trees surrounded by other highly defoliated trees) and ‘cold spot trees’ (lightly defoliated trees surrounded by other lightly defoliated trees) within each plot using local Getis-Ord Gi* analysis. Results revealed that 11 to 27 plots had hot spot trees and 27% to 64% of them had mean defoliation <25%, while plots with 75% to 100% defoliation had either cold spot trees or non-significant spots, which suggested that whether defoliation was high or low enough to be a hot or cold spot depended on the defoliation level of the entire plot. We fitted individual-tree balsam fir defoliation regression models as a function of plot and surrounding tree characteristics (using search radii of 3–5 m). The best model contained plot average balsam fir defoliation and subject tree basal area, and these two variables explained 80% of the variance, which was 2% to 5% higher than the variability explained by the neighboring tree defoliation, over the 3–5 m search radii tested. We concluded that plot-level defoliation and basal area were adequate for modeling individual tree defoliation, and although clustering of defoliation was evident, larger plots were needed to determine the optimum neighborhood radius for predicting defoliation on an individual. Spatial autocorrelation analysis can serve as an objective way to quantify such ecological patterns.


1989 ◽  
Vol 19 (12) ◽  
pp. 1616-1624 ◽  
Author(s):  
Harald Piene

Trees defoliated by the spruce budworm (Choristoneurafumiferana (Clem.)) for 1 to 4 years and subsequently protected rapidly regained foliar biomass. Three plots of 25- to 30-year-old balsam fir (Abiesbalsamga (L.) Mill.) trees, on the Cape Breton Highlands of Nova Scotia, were studied. Two major factors contributed to the rapid growth recovery rates: the ability to produce epicormic shoots, combined with increased retention of older age-classes of needles, and the development of new foliage at the expense of volume growth. A complete recovery of volume increment occurred after 2 years of extreme defoliation, but not after 4 years of severe defoliation. Epicormic shoot production was only associated with shoot and bud destruction and therefore, growth recovery was slow after partial defoliation of only current foliage. In all plots studied, there was a lag of 2 to 3 years between increased foliar biomass and significant increases in volume increment.


1995 ◽  
Vol 25 (8) ◽  
pp. 1375-1384 ◽  
Author(s):  
Yves Bergeron ◽  
Alain Leduc ◽  
Claude Joyal ◽  
Hubert Morin

Balsam fir (Abiesbalsamea (L.) Mill.) mortality caused by the last spruce budworm (Choristoneurafumiferana (Clem.)) outbreak (1970–1987) was studied in 624 sites belonging to a complex natural forest mosaic originating from different fires in northwestern Quebec. Multiple regression analyses were used to assess the respective effects of stand structure, species composition, site characteristics, and the forest composition surrounding the stand on observed stand mortality. Mortality was observed to increase in relation to diameter of the trees, basal area of balsam fir, and the number of stands dominated by conifers in the forest mosaic. All of these factors showed significant independent effects, but 60% of the variance remained unexplained. Site characteristics, however, did not show a significant relationship to stand mortality. The results suggest that forest composition at both the stand and the forest mosaic levels may be responsible for differing degrees of defoliation that result in differences in stand mortality. Forest management strategies that favor the presence of mixed compositions both at the stand level and at the mosaic level may contribute to decreased stand vulnerability.


1985 ◽  
Vol 61 (2) ◽  
pp. 75-80 ◽  
Author(s):  
Harold O. Batzer ◽  
Michael P. Popp

Plots in 24 spruce-fir stands in northeastern Minnesota studied throughout the period 1957 to 1962 at the time of a spruce budworm outbreak were remeasured in 1979. Composition of the overstory changed from an average of 79% of the basal area in host species before to 31% after the budworm outbreak. Twelve percent of the stands showed growth in nonhost species that more than offset the loss in balsam fir and white spruce. The understory was minimally stocked with balsam fir in two-thirds of the stands. Only 4% of the regeneration was spruce. Even so, some well-established white spruce seedlings were found in two-thirds of the stands. Red maple was the most abundant hardwood invader. Raspberry, hazel and mountain maple were the principal shrub species limiting balsam fir reproduction Shrubs were most abundant in stands where balsam fir mortality had exceeded 80%. Half of the stands had seedlings that originated both before and after the outbreak; 45% had seedlings that originated only after the outbreak; and 5% had seedlings that originated only before the outbreak. Stands having moderate mixture of nonhost species in the over-story prior to the budworm outbreak had the most balsam fir regeneration. This resulted from seed produced by surviving balsam fir trees after the outbreak. Key words: Choristoneura fumiferana, Abies balsamea, Balsam fir, spruce-fir shrubs


Sign in / Sign up

Export Citation Format

Share Document