Seedling responses to forest canopy disturbance following a spruce budworm outbreak in Maine

1994 ◽  
Vol 24 (4) ◽  
pp. 850-859 ◽  
Author(s):  
Akira Osawa

Patterns of tree mortality and seedling responses to canopy disturbance were investigated in northern Maine, where an outbreak of the spruce budworm (Choristoneurafumiferana (Clem.)) affected the forests of balsam fir (Abiesbalsamea (L.) Mill.) and spruce (Picea spp.) continuously between 1972 and 1984. The outbreak created a gradient of canopy tree mortality that ranged between 8.5 and 100% of the cumulative basal area in 1984. This was a result of the difference in vulnerability among the host species (balsam fir > spruce) and of their spatial distribution patterns along the site drainage gradient. Two groups of plant species responded differently to the gradient of canopy disturbance: balsam fir, spruce, and white birch (Betulapapyrifera Marsh.) regenerated mostly at the intermediate levels of mortality (≈20%by basal area) of the canopy balsam fir; raspberry (Rubusidaeus L.) and pin cherry (Prunuspensylvanica L.) were most abundant at ≈100% fir mortality. Overall, the observed responses in space and time of the seedlings to budworm-caused canopy disturbance could be mostly explained by the concept of patch dynamics. Long-term changes in species composition of the spruce–fir forests cannot be predicted with precision with the present knowledge. However, I hypothesize, based on the species-specific vulnerability to budworm damage and patterns of regeneration, that the proportion of spruce to fir trees would not differ very much in the long run regardless of extensive tree mortality by the spruce budworm.

1994 ◽  
Vol 24 (11) ◽  
pp. 2208-2221 ◽  
Author(s):  
Marie R. Coyea ◽  
Hank A. Margolis

The growth efficiencies (E; stemwood growth per unit leaf area) of balsam fir (Abiesbalsamea (L.) Mill.) trees from 20 stands were reconstructed over the 30-year period from 1960 to 1989 in order to determine if E could be used to predict tree mortality occurring during and after an epidemic of eastern spruce budworm (Choristoneurafumiferana (Clem.)). Growth efficiencies were reconstructed based on the relationship between age and the number of annual growth rings in the cross-sectional area of heartwood at breast height (R2 = 0.97) and on the previously demonstrated relationship between sapwood area and leaf area of balsam fir across a wide geographic area. Profile and logistic regression analyses demonstrated that apparent E (i.e., the historically reconstructed E) of surviving trees was greater than that of dead trees for every year of the 30-year analysis period. For trees in the 25- to 35-year age-class in 1960, apparent E was the only variable measured prior to the epidemic that was significantly related to balsam fir mortality. For all trees (aged 11 to 46 years in 1960), both tree age and apparent E were significant factors prior to the epidemic. During and following the epidemic, several of the more standard mensurational variables (e.g., diameter and basal area growth) were also significantly associated with balsam fir mortality, but apparent E had the highest levels of significance. Using logistical regression, critical E values below which trees would be predicted to die were calculated as 5-year running averages for the period prior to the epidemic (1960–1968). These were stable at around 0.17 × 10−4 m2 basal area growth•(m2 leaf area)−1•year−1. Following the epidemic, critical E values were again stable but at a lower level of around 0.07. There was a negative exponential relationship between apparent E and leaf area. Furthermore, for the same level of leaf area, surviving trees had a higher apparent E than trees that died, up to approximately 30 m2 of leaf area. These results suggest that growth efficiency should be considered as part of standard forest inventories in the balsam fir zone because of its ease of measure and its apparent ability to provide a sensitive, physiologically based index of forest health. Furthermore, the technique of historically reconstructing E demonstrated in this study may be of interest for other types of dendrochronological research.


1958 ◽  
Vol 34 (4) ◽  
pp. 405-422 ◽  
Author(s):  
J. R. Blais

The annual defoliation by spruce budworm and the progressive mortality of balsam fir trees were recorded in nine study plots in northwestern Ontario over a period of 11 years. In addition to general observations on the relationship of tree mortality to defoliation, some information was obtained on the relative vulnerability of the trees with respect to size, physiological age (flowering condition), and vigor (site quality).


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.


1984 ◽  
Vol 60 (5) ◽  
pp. 273-279 ◽  
Author(s):  
David A. MacLean

Effects of spruce budworm (Choristoneura fumiferana (Clem.)) outbreaks on the productivity and stability of forests in eastern Canada are reviewed and discussed. Defoliation results in reduced growth of trees, widespread tree mortality, and loss of wood production, and thereby causes major forest management problems. At present, the only feasible method for limiting damage and losses from budworm outbreaks over large areas is to apply chemical or biological insecticides periodically to kill larvae and protect the forest from defoliation and tree mortality. Although budworm outbreaks definitely disrupt the wood-producing capacity of forests (or the short-term "stability of forests for human usage"), in terms of overall ecological stability, outbreaks apparently act as a cycling mechanism that allows advance fir-spruce regeneration to succeed the fir-spruce overstory.


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


1992 ◽  
Vol 22 (11) ◽  
pp. 1701-1711 ◽  
Author(s):  
Lucie Bertrand ◽  
Louis Bélanger ◽  
Robert L. Beauregard

Models of compatible volume and basal area growth and yield covering a period of 10 to 45 years after harvesting were developed for second growth boreal stands of balsam fir (Abiesbalsamea (L.) Mill.). The 131 permanent plots used for the study were located near Matane, in the Gaspé Peninsula, and are part of the balsam fir–white birch ecoclimatic domain. These stands were harvested in 1934, 1944, and 1953, using a manual cut-and-bunch harvesting method that protected advance growth, and measures were taken in 1954, 1964, and 1978. The stands were moderately affected by spruce budworm outbreaks between 1950–1957 and 1975–1978. Years elapsed since release rather than total age was used as the temporal variable. Even though the characteristics of the coniferous natural regeneration were quite variable, total basal area explained an important part of growth variations of young fir stands by integrating both density and dimensions of the regeneration. Results show, within the limits of the observed densities (< 15 000 stems/ha, 10 years after harvesting), that stands with a higher basal area will have higher total and merchantable volumes at a given age; rotation age for maximum volume production will decrease correspondingly. Abundance of saplings in the initial natural regeneration can thus have an important impact on stand production and rotation age. In the case of nonoverdense young fir stands (< 15 000 stems/ha, 10 years after harvesting with no height growth impediment), the use of spacing treatments that significantly reduce total basal area could be questioned when pursuing maximum fiber production.


1982 ◽  
Vol 12 (4) ◽  
pp. 780-787 ◽  
Author(s):  
R. I. Alfaro ◽  
G. A. Van Sickle ◽  
A. J. Thomson ◽  
E. Wegwitz

The effects of defoliation by western spruce budworm (Choristoneuraoccidentalis (Freeman)), on Douglas-fir (Pseudotsugamenziesii (Mirb.) Franco) radial growth at breast height and tree mortality are given. Four hundred and twenty trees were marked in an 81-year-old stand, and their defoliation levels were recorded annually from 1970 to 1980 in an outbreak that lasted from 1970 to 1974, inclusive. Forty-one trees were felled and dissected in 1977, 3 years after recovery began. The number of stems per hectare was reduced by 39.3% and basal area by 11.6% through mortality, most occurring among the small diameter, suppressed, and intermediate trees. Relationships were established between mortality and defoliation. Radial increments were examined, and the presence of four outbreaks during the life of the stand was detected. The combined effect of these infestations amounted to a loss of about 12% of the estimated potential diameter had not the insects been active. The most recent outbreak (1970–1974) caused a total of 10 years of subnormal growth, including 5 years due to defoliation and 5 years of recovery. The relationship between radial increment losses and defoliation intensity and duration is studied and quantified.


1999 ◽  
Vol 75 (3) ◽  
pp. 515-534 ◽  
Author(s):  
Pierre Pominville ◽  
Stéphane Déry ◽  
Louis Bélanger

An outbreak of spruce budworm, Choristoneura fumiferana (Clem.), occurred between 1974 and 1987, in Quebec, in the eastern balsam fir, Abies balsamea (L.) Mill, - yellow birch, Betula alleghaniensis Britton, ecoclimatic sub-domain. The effect of this disruption has been assessed in mesic balsam fir stands killed during the outbreak, in mesic balsam fir stands partially damaged and in the following stands, also partially damaged: mesic yellow birch – balsam fir stands, mesic white birch, Betulapapyrifera Marsh., - balsam fir stands, mesic balsam fir – yellow birch stands, mesic balsam fir – white birch stands and xeric balsam fir stands. To that effect, surveys were led before, immediately after, and about five years after the outbreak in two blocks that have not been protected with insecticides. These blocks, located in Charlevoix and in Shipshaw management units, are second growth stands originating from clearcuts which occured about 50 years ago. Approximately five years after the outbreak, abundant coniferous regeneration was found everywhere except in the mesic yellow birch –balsam fir stand and in the dead mesic balsam fir stand, where softwood represented less than 50% of the regeneration. On the other hand, young softwood stems were located under the regeneration of white birch and of mountain maple, Acer spicatum Lam, in dead balsam fir stands, in balsam fir – white birch stands, as well as in living balsam fir stands and under mountain maple in yellow birch – balsam fir stands and in balsam fir – yellow birch stands. Our age structures indicate that softwood advance growth was relatively rare in these stands. Thus, during the opening of the canopy by the spruce budworm, intolerant hard-woods and shrubs invaded the still available microsites. In the dead balsam fir stands, stocking of the dominant hardwood regeneration stems is equivalent to that of softwood. Thus, dead balsam fir stands are turning to mixed stands. Xeric stands will remain softwood stands since they show luxuriant softwood regeneration dominating in height. In the other stands, we will have to wait the harvest period before we can adequately assess succession.


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.


1996 ◽  
Vol 26 (12) ◽  
pp. 2099-2108 ◽  
Author(s):  
David A. MacLean ◽  
Wayne E. MacKinnon

The accuracy of aerial sketch-mapping estimates of spruce budworm (Choristoneurafumiferana (Clem.)) defoliation was evaluated from 1984 to 1993 in 222–325 sample plots in spruce (Picea sp.)–balsam fir (Abiesbalsamea (L.) Mill.) stands in New Brunswick. Operational aerial defoliation estimates were used, wherein all productive forest in known budworm infestation zones was surveyed each year from small aircraft with flight lines 2–5 km apart, and rated in classes of nil (0–10%), light (11–30%), moderate (31–70%), and severe (71–100%). Aerial defoliation estimates were compared with ground-based binocular estimates of current defoliation for an average of 10 trees/plot (range 5–20). Overall, 56% of plots were correctly rated by aerial sketch mapping in four classes (nil, light, moderate, and severe), with 37% of the plots underestimated and 7% overestimated. The predominant error (26% of plots) was rating defoliation as nil (0–10%) from the air when it was actually light (11–30%). This error was deemed not important in terms of predicting tree response, since data from the literature indicated that defoliation less than 30% did not cause tree mortality, although if continued, it would reduce growth. Using three defoliation classes (by combining nil and light, 0–30%), 82% of the plots were correctly classified by aerial sketch mapping. The probability of correct aerial classification of defoliation was significantly affected by defoliation class, weather conditions prior to and during observation flights, and the defoliation class × weather interaction. It was concluded that aerial sketch mapping of spruce budworm defoliation is a viable technique that can be used for both surveys and decision support systems that estimate forest response to budworm outbreaks and management activities.


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