Carry-over effect of host nutritional quality on performance of spruce budworm progeny

2011 ◽  
Vol 102 (3) ◽  
pp. 275-284 ◽  
Author(s):  
A. Fuentealba ◽  
É. Bauce

AbstractThe effect of host nutritional quality on spruce budworm (Choristoneura fumiferana (Clemens)) parental and offspring performance was studied using field and laboratory rearing experiments, and foliar chemical analyses. Foliage of balsam fir (Abies balsamea (L.) Mill.), white spruce (Picea glauca (Moench) Voss) and black spruce (P. mariana (Mill.) BSP) was used to rear the parental generation in the field, whereas an artificial diet was used to rear the progeny under laboratory conditions. Important differences in the food quality were provided by the three hosts. Black spruce foliage had higher concentrations of certain monoterpene deterrents and total phenolics, together with stronger seasonal declines in nutrients such as N, P and Mg, compared with the other hosts. We hypothesise that this trend may be related to poor performance and survival of the progeny. Laboratory rearing showed that progeny of parents that fed on black spruce exhibited longer developmental times and greater mortality, and had lower pupal mass than progeny of parents fed on the other hosts. Further, artificial food-fed progeny of insects reared on black spruce reached sixth-instar later, with lower mass, and exhibited higher relative growth rate (RGR) than progeny of parents fed on the other hosts. These results suggest nutritionally-based parental effects. These results also confirmed that the quality of food consumed by the parents can influence the fitness of the next generation.

1957 ◽  
Vol 33 (4) ◽  
pp. 364-372 ◽  
Author(s):  
J. R. Blais

Spruce budworm larvae feeding on black spruce had a lower rate of development and a higher rate of mortality than those feeding on white spruce or balsam fir. This was attributable to the lateness in opening of the black spruce buds rather than to the inferior nutritional quality of the foliage. When staminate flowers were present in abundance on black spruce trees, development and survival of the insect was fairly similar to that on the other two species of trees; the flowers provided adequate food at the time of the third and fourth instars thus permitting the larvae to survive until the opening of the shoot buds. The late opening of the black spruce buds explains the relative immunity of this species to severe spruce budworm damage.


1984 ◽  
Vol 116 (1) ◽  
pp. 101-102 ◽  
Author(s):  
O. N. Morris

Bacillus thuringiensis var. kurstaki (B.t.) is the most widely used biological control agent against the spruce budworm, Choristoneura fumiferana (Clem.), a major defoliator of coniferous forests. The technology of applying the bacterium, however, is still not fully developed and the strategy of applying single or split applications of B.t. in unmixed stands is still in question. Double applications are generally accepted as necessary in mixed stands of white spruce, Picea glauca (Moench) Voss, red spruce, P. rubens Sarg., black spruce, P. mariana (Mill.) BSP, and balsam fir, Abies balsamea (L.) Mill., due to difference in the phenological development of the host trees and of the budworm infesting them. Field trials were conducted at Mine Centre, Ontario, to compare the efficacies of double and single applications of B.t. against the budwonn infesting balsam fir stands.


2020 ◽  
Vol 50 (6) ◽  
pp. 565-580
Author(s):  
Yuanyuan Wu ◽  
David A. MacLean ◽  
Chris Hennigar ◽  
Anthony R. Taylor

Defoliation level and site type are thought to influence tree response during spruce budworm (Choristoneura fumiferana (Clemens)) outbreaks. We determined the effects of four manual defoliation treatments (0%, 50%, 100%, and 100% + bud removal of current foliage) for 3 years on foliage production of balsam fir (Abies balsamea (L.) Mill.), black spruce (Picea mariana (Mill.) Britton, Sterns & Poggenb.), and white spruce (Picea glauca (Moench) Voss) trees on four site-quality classes. After 3 years of defoliation and 2 years of recovery, foliage biomass was reduced by 34%–98%. During defoliation, the number of shoots generally increased and shoot length of spruce generally decreased, especially on rich sites. During recovery, the number of shoots increased substantially, shoot length decreased, and bud destruction reduced the number of shoots by about 50% compared with that of trees that received the 100% defoliation treatment. Defoliation did not substantially affect needle length. Trees on rich sites had two- to fourfold greater foliage production than trees on poor sites. Effects of site and defoliation differed among species, but site quality, especially nutrition, played an important role in production of shoots and needles and the tree’s ability to withstand defoliation. Black spruce had more limited ability to recover foliage biomass, only producing more shoots, whereas balsam fir and white spruce had stronger ability to recover needle and shoot length, respectively.


2004 ◽  
Vol 34 (11) ◽  
pp. 2351-2362 ◽  
Author(s):  
Wayne E MacKinnon ◽  
David A MacLean

The species composition of surrounding forest and site characteristics have been postulated to influence growth loss caused by eastern spruce budworm (Choristoneura fumiferana Clem.) defoliation. Forty spruce (Picea spp.) and balsam fir (Abies balsamea (L.) Mill.) stands located in north-central New Brunswick, Canada, were measured for defoliation and tree growth and used to determine the effects of surrounding forest (softwood, mixedwood), site (wet soil – nutrient poor; moist soil – nutrient rich), and species group (balsam fir, spruce) on growth reduction caused by spruce budworm. Stem analysis of six trees per stand (total 240 trees) determined mean specific volume increment (SVI) per year in 1973–1993. There was relatively little defoliation during the 1989–1993 measurement period, and regression analyses showed that SVI was significantly (p = 0.0299) related to mean defoliation for only one of eight treatment classes: balsam fir on moist–rich sites in mixedwood forests. However, two periods of earlier growth reduction were evident, and analysis of variance showed that balsam fir on wet–poor sites sustained 12% greater (p = 0.0071) reduction in SVI from 1987 to 1990 than balsam fir on moist–rich sites. White spruce (Picea glauca (Moench) Voss) sustained 13% greater (p = 0.0198) reduction in SVI from 1973 to 1978 than red spruce (Picea rubens Sarg.) – black spruce (Picea mariana (Mill.) BSP). Surrounding forest type did not significantly affect SVI reduction from 1973 to 1978 or from 1987 to 1990, but from 1973 to 1978 stands in softwood forest sustained 5%–8% more growth reduction than those in mixedwood forest.


1971 ◽  
Vol 49 (7) ◽  
pp. 1005-1011 ◽  
Author(s):  
J. P. Kimmins

The amino acids of new and old foliage of flowering and non-flowering balsam fir (Abies balsamea (L.) Mill.) and white spruce (Picea glauca (Moench) Voss) were investigated using two-dimensional descending paper chromatography. The data were analyzed for variation associated with age of foliage, age of tree, and flowering condition. The concentration of foliar amino acids was greater in balsam fir than in white spruce, and greater in new foliage than old foliage.The difference in concentration between foliage of flowering and non-flowering trees was smaller. However, the new foliage of flowering fir had higher levels of most of the amino acids examined than any other foliage category. This appears to reflect the known suitability of these foliage categories for spruce budworm larvae. While the data presented do not quantify the ecological significance of this apparent correlation, they do support the theory that variations in the nutritional quality of host plants play a very important role in the dynamics of herbivore populations.


1958 ◽  
Vol 34 (1) ◽  
pp. 39-47 ◽  
Author(s):  
J. R. Blais

The relationship between spruce budworm defoliation and radial growth at breast height for balsam fir and white spruce trees of merchantable size was studied in various stands in northwestern Ontario. Defoliation was recorded yearly for these stands from the beginning of the infestation, and radial growth measurements were obtained from increment cores. The first year of radial growth suppression was calculated by comparing the growth of the affected species with that of jack pine and red pine trees by means of a growth-ratio technique. Apparent suppression in balsam fir and white spruce varied between stands, and, generally, occurred at the earliest in the second year and at the latest in the fourth year of severe defoliation. A wide ring at the base of the tree coinciding with the first year of suppression as reported by Craighead was non-existent.


1975 ◽  
Vol 107 (7) ◽  
pp. 717-728 ◽  
Author(s):  
G. T. Harvey

AbstractAmylopectin added to a sugar-free wheat-germ diet was equal to or better than sucrose as a carbohydrate source, and appears to be readily utilized by the eastern spruce budworm (Choristoneura fumiferana (Clem.)). Larval growth on diets containing dextrins or potato starch shows that they are partly utilized. Starches from other sources, including those isolated from mature balsam fir (Abies balsamea (L.) Mill.) or white spruce (Picea glauca (Moench) Voss) needles, are not utilized to any extent, on the basis of larval growth on diets to which they have been added.Sixth-instar budworm reared on artificial diets contain amylase(s) in midgut and salivary gland homogenates, which show a low rate of digestion of starches from host foliage. However, the presence of appreciable starch in frass from foliage-fed insects and the apparent low utilizability of foliar starch indicate that the latter is not an important nutrient for the budworm under natural conditions.


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 (10) ◽  
pp. 850 ◽  
Author(s):  
Janie Lavoie ◽  
Miguel Montoro Girona ◽  
Hubert Morin

Spruce budworm (Choristoneura fumiferana) is the main defoliator of conifer trees in North American boreal forests, affecting extensive areas and causing marked losses of timber supplies. In 2017, spruce budworm affected more than 7 million ha of Eastern Canadian forest. Defoliation was particularly severe for black spruce (Picea mariana (Mill.) B.S.P.), one of the most important commercial trees in Canada. During the last decades, intensive forest exploitation practices have created vast stands of young balsam fir (Abies balsamea (L.) Mill.) and black spruce. Most research focused on the impacts of spruce budworm has been on mature stands; its effects on regeneration, however, have been neglected. This study evaluates the impacts of spruce budworm on the defoliation of conifer seedlings (black spruce and balsam fir) in clearcuts. We measured the cumulative and annual defoliation of seedlings within six clearcut black spruce stands in Quebec (Canada) that had experienced severe levels of defoliation due to spruce budworm. For all sampled seedlings, we recorded tree species, height class, and distance to the residual forest. Seedling height and species strongly influenced defoliation level. Small seedlings were less affected by spruce budworm activity. As well, cumulative defoliation for balsam fir was double that of black spruce (21% and 9%, respectively). Distance to residual stands had no significant effect on seedling defoliation. As insect outbreaks in boreal forests are expected to become more severe and frequent in the near future, our results are important for adapting forest management strategies to insect outbreaks in a context of climate change.


1993 ◽  
Vol 125 (3) ◽  
pp. 479-488 ◽  
Author(s):  
Beresford L. Cadogan ◽  
Roger D. Scharbach

AbstractThe insecticide Foray 48B (Bacillus thuringiensis var. kurstaki Berliner) was applied undiluted at 30 BIU per ha to control spruce budworm, Choristoneura fumiferana (Clem.), in a mixed boreal forest stand of balsam fir, Abies balsamea (L.) Mill., and black spruce, Picea mariana (Mill.) B.S.P. When the treatment was timed to coincide with the early flushing of balsam fir shoots, the corrected budworm population reductions were 74 and 52% on balsam fir and black spruce, respectively. This treatment resulted in 19 and 8% defoliation on the two respective species. When the insecticide application was timed later to coincide with the late flushing of black spruce shoots the corrected population reductions were 93% on balsam fir and 72% on black spruce. Defoliation of the two species was 29 and 10% respectively, following this treatment. Larval survival on both species after the spray timed for black spruce (0.8 and 2.2 larvae per 45-cm branch on balsam fir and black spruce, respectively) was significantly less (P = 0.05) than that observed after the spray timed for balsam fir (4.6 and 4.2 larvae per 45-cm branch on the respective host species).The data indicate that the spray timed to correspond with the flushing of black spruce was generally more efficacious than the spray timed to impact on newly flushed balsam fir; nevertheless, the results raise the question as to how B. thuringiensis insecticides impact on early-instar budworm larvae when there is no preferred current year foliage on which the insects can feed.


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