Spatial and temporal patterns of balsam fir mortality in spaced and unspaced stands caused by spruce budworm defoliation

1995 ◽  
Vol 25 (6) ◽  
pp. 902-911 ◽  
Author(s):  
David A. MacLean ◽  
Harald Piene

Spatial and temporal patterns of balsam fir (Abiesbalsamea (L.) Mill.) mortality were studied during a spruce budworm (Choristoneurafumiferana Clem.) outbreak from 1976 to 1984 on Cape Breton Island, Nova Scotia. Natural mortality in four insecticide-protected plots was 0% in spaced and 9–15% in unspaced stands, with only the smallest trees dying. Budworm-caused mortality (i.e., total minus natural) was 31–49% and 11–32% in spaced and unspaced young fir plots, respectively, but reached 94–100% in severely defoliated spaced plots, unprecedented in the literature for young fir mortality caused by the spruce budworm. Mortality began in the fourth to sixth year of defoliation, being earliest in the severely defoliated plots. From 80 to 90% of trees that died had > 75% cumulative defoliation, and most (64–100%) of the smallest (2 cm DBH) trees died. There was no significant difference in percent mortality between 25 spaced and 13 unspaced plots (p = 0.434), although, on average, mortality was 10–22% higher in the spaced plots. About 20–30% more of the intermediate-sized and largest trees were killed in the spaced plots. High spatial plot to plot variability in mortality occurred, which was apparently related to observed differences in the amount of defoliation and especially the incidence of "back-feeding" (damage to noncurrent foliage), as well as to plot size. Because budworm-caused mortality exhibits a distribution that tends to form large "holes" in stands, the degree of between-plot variability is related to plot size, and it is recommended that small plots that may miss these patches of mortality be avoided.

1995 ◽  
Vol 25 (7) ◽  
pp. 1128-1136 ◽  
Author(s):  
Donald P. Ostaff ◽  
David A. MacLean

Changes in foliar production caused by spruce budworm (Choristoneurafumiferana (Clem.)) defoliation and patterns of volume increment of surviving trees during and after the outbreak were determined in 20 mature balsam fir (Abiesbalsamea (L.) Mill.) stands on Cape Breton Island, Nova Scotia. Following the cessation of defoliation, the number of shoots increased 4-fold and mean shoot length doubled, resulting in a 12-fold increase in needle biomass. Average specific volume increment declined from 0.17–0.25 to 0.02–0.04 cm3•cm−2•year−1 after 4 years of severe defoliation; maximum increment reduction was 74–92%. Periodic radial increment and volume increment reduction (percent of mean increment in the previous decade) were both significantly related to cumulative (summed current annual) defoliation; a logistic regression equation explained 77% of the variation in volume loss. Differences in growth recovery among trees were determined by the temporal patterns of defoliation, with a 1-year lag before the beginning of volume increment recovery. Following 5 to 8 years of recovery, surviving trees had regained 48–82% of their predefoliation increment; however, absolute volume losses during the outbreak averaged 12–33 dm3/tree, or 32–48%.


1989 ◽  
Vol 19 (9) ◽  
pp. 1087-1095 ◽  
Author(s):  
David A. MacLean ◽  
Donald P. Ostaff

Tree mortality caused by spruce budworm (Choristoneurafumiferana (Clem.)) defoliation was assessed annually from 1976 to 1985 in 20 mature balsam fir (Abiesbalsamea (L.) Mill.) stands on Cape Breton Island, Nova Scotia, and was related to defoliation and to tree, stand, and site characteristics. Ten to 12 years after the start of the budworm outbreak, fir mortality averaged 87% of the merchantable volume (range 60–100%) among the stands. Timing of mortality was similar to that found in studies of previous outbreaks. In the first 4 years of the outbreak, virtually all the trees that died had more than 90% cumulative defoliation but, overall, 64, 21, and 14% of the dead trees had cumulative defoliation >90, 76 to 90, and 51 to 75%, respectively. Early in the outbreak, fir mortality was generally negatively correlated with tree vigor, relative crown position, or diameter at breast height, but in later years, trees were killed irrespective of these factors. Fir mortality was evenly distributed among different sized trees, and 73 to 86% of the trees in each 5 cm diameter at breast height class died. A linear regression equation between dead fir volume and total fir volume explained 89% of the variability in mortality among stands. Percent fir mortality was correlated (r = 0.84) with visual estimates of cumulative defoliation (including all age-classes of foliage) in 1981, but mortality was not correlated with cumulative current annual defoliation or with site characteristics. Using regression equations, fir mortality during this budworm outbreak was predicted to within ±6 m2/ha in 14 of 18 (78%) of the stands, with a relative accuracy of 17.7%.


1989 ◽  
Vol 19 (9) ◽  
pp. 1077-1086 ◽  
Author(s):  
Donald P. Ostaff ◽  
David A. MacLean

Effects of an uncontrolled spruce budworm (Choristoneurafumiferana (Clem.)) outbreak in 20 mature balsam fir (Abiesbalsamea (L.) Mill.) stands on Cape Breton Island, Nova Scotia, were studied from 1976 to 1985. Spruce budworm populations were extremely high, higher than peak levels recorded for other outbreaks, and averaged over 380 third-instar larvae per square metre of foliage from 1976 to 1980. As many as 1570 third-instar larvae per square metre occurred 5 to 7 years after the start of the outbreak, resulting in complete current defoliation and back-feeding on older foliage. Stands were divided into three groups, based on the pattern of cumulative current defoliation; the sum of current annual defoliation during the outbreak was 343, 445, and 543% for these groups, equivalent to the removal of 3.5 to 5.5 age-classes of foliage. Budworm defoliation caused the death of 78, 80, and 89% of the merchantable balsam fir volume in the three groups of stands, respectively, as well as 27% of the spruce (Picea sp.) volume; another 39% of the spruce volume died as a result of spruce beetle (Dendroctonusrufipennis Kby.) activity. Fir mortality commenced 3 years after the start of the outbreak and spruce mortality 2 to 3 years later. About one-half of the total mortality occurred in the 4 years after budworm populations and defoliation returned to low levels. Tree mortality and loss of foliage opened the stands, and 4 years after the collapse of the outbreak, 4% of the surviving trees and 17% of the dead trees had blown down, whereas 60% of all trees had broken tops.


1996 ◽  
Vol 128 (6) ◽  
pp. 1109-1113 ◽  
Author(s):  
Harald Piene

AbstractDetailed estimates of defoliation caused by spruce budworm [Choristoneura fumiferana (Clem.)] over the crown length of young balsam fir [Abies balsamea (L.) Mill.] were made throughout a spruce budworm outbreak from 1976 to 1984 in the Cape Breton Highlands, Nova Scotia. The results show no clear tendency for a particular level of the crown to be damaged more heavily than any other. Thus, there is no reason to continue the common practice of taking samples from the mid-crown level on the assumption that they represent an ‘average’ level of defoliation either for high or low populations. Sampling from the bottom of the crown should provide a more convenient and cost-effective approach for estimating defoliation.


Forests ◽  
2018 ◽  
Vol 9 (9) ◽  
pp. 513 ◽  
Author(s):  
Zelin Liu ◽  
Changhui Peng ◽  
Louis De Grandpré ◽  
Jean-Noël Candau ◽  
Xiaolu Zhou ◽  
...  

The spruce budworm (SBW) defoliates and kills conifer trees, consequently affecting carbon (C) exchanges between the land and atmosphere. Here, we developed a new TRIPLEX-Insect sub-model to quantify the impacts of insect outbreaks on forest C fluxes. We modeled annual defoliation (AD), cumulative defoliation (CD), and tree mortality. The model was validated against observed and published data at the stand level in the North Shore region of Québec and Cape Breton Island in Nova Scotia, Canada. The results suggest that TRIPLEX-Insect performs very well in capturing tree mortality following SBW outbreaks and slightly underestimates current annual volume increment (CAI). In both mature and immature forests, the simulation model suggests a larger reduction in gross primary productivity (GPP) than in autotrophic respiration (Ra) at the same defoliation level when tree mortality was low. After an SBW outbreak, the growth release of surviving trees contributes to the recovery of annual net ecosystem productivity (NEP) based on forest age if mortality is not excessive. Overall, the TRIPLEX-Insect model is capable of simulating C dynamics of balsam fir following SBW disturbances and can be used as an efficient tool in forest insect management.


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.


1984 ◽  
Vol 14 (3) ◽  
pp. 404-411 ◽  
Author(s):  
H. Piene ◽  
D. A. MacLean

Growth response of young, spaced balsam fir (Abiesbalsamea (L.) Mill.) to 3 successive years (1979–1981) of treatment with Bacillusthuringiensis Berliner for spruce budworm (Choristoneurafumiferana (Clem.)) control was examined in 20 plots on the Cape Breton Highlands, Nova Scotia. Defoliation commenced in 1976, 3 years before control operations began. Five plots were established both inside and outside the spray block, in areas that had been severely defoliated by budworm and in areas moderately defoliated. All plots in the severely defoliated area suffered heavy tree mortality, but mortality was significantly lower in the protected plots. In contrast, the moderately defoliated plots suffered virtually no tree mortality. The average volume increment of stem-analyzed trees from 1979 to 1981 was 0.63 dm3/tree for protected and 0.43 dm3/tree for unprotected trees in the severely defoliated area versus 4.15 dm3/tree for protected and 3.08 dm3/tree for unprotected trees in the moderately defoliated area. These volume increment values are equivalent to 8.8 m3/ha of growth between 1979 and 1981 for protected plots in the moderately defoliated area, compared with 6.1 m3/ha for unprotected plots. Therefore, a total gain of 2.7 m3/ha can be attributed to the 3 years of B. thuringiensis spraying. Long-term growth responses toB. thuringiensis spraying were not evaluated. Better results would be expected had protection started at the beginning of the budworm outbreak, instead of after 3 years of severe defoliation.


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