scholarly journals Avian Predation in a Declining Outbreak Population of the Spruce Budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae)

Insects ◽  
2021 ◽  
Vol 12 (8) ◽  
pp. 720
Author(s):  
Jacques Régnière ◽  
Lisa Venier ◽  
Dan Welsh
Keyword(s):  
Foraging Behavior ◽  
Picea Glauca ◽  
Choristoneura Fumiferana ◽  
Feeding Activity ◽  
Abies Balsamea ◽  
Bird Species ◽  
Spruce Budworm ◽  
White Spruce ◽  
Avian Predation ◽  
The Impact

The impact of avian predation on a declining population of the spruce budworm, Choristoneura fumifereana (Clem.), was measured using single-tree exclosure cages in a mature stand of balsam fir, Abies balsamea (L.), and white spruce, Picea glauca (Moench.) Voss. Bird population censuses and observations of foraging and nest-feeding activity were also made to determine the response of budworm-linked warblers to decreasing food availability. Seasonal patterns of foraging. as well as foraging success in the declining prey population was compared to similar information from birds observed in another stand where the spruce budworm population was rising. Avian predation was an important source of mortality between the 4th instar and moth emergence in the declining outbreak population. Mortality by predation increased from negligible to over 98% as budworm density dropped from 100 to <1 larva/kg of host foliage, over 3 years. Calculations based on nest-feeding activity and basic metabolic demands support these observed rates. Seasonal and yearly differences in predation rates observed between the two host-tree species correspond to equivalent shifts in bird foraging behavior in response to dropping insect density. In particular, a preference for searching on white spruce disappeared, although budworm-linked birds remained more efficient at finding food on this plant. The ability to change foraging behavior as prey density dropped differed between bird species.

Variations in the foliar amino acid composition of flowering and non-flowering balsam fir (Abies balsamea (L.) Mill.) and white spruce (Picea glauca (Moench) Voss) in relation to outbreaks of the spruce budworm (Choristoneura fumiferana (Clem))

1971 ◽  
Vol 49 (7) ◽  
pp. 1005-1011 ◽  
Author(s):  
J. P. Kimmins
Keyword(s):  
Amino Acids ◽  
Picea Glauca ◽  
Host Plants ◽  
Choristoneura Fumiferana ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
White Spruce ◽  
Balsam Fir ◽  
Apparent Correlation

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.

scholarly journals EFFECTS OF DEFOLIATION BY SPRUCE BUDWORM (CHORISTONEURA FUMIFERANA CLEM.) ON RADIAL GROWTH AT BREAST HEIGHT OF BALSAM FIR (ABIES BALSAMEA (L.) MILL.) AND WHITE SPRUCE (PICEA GLAUCA (MOENCH) VOSS.)

1958 ◽  
Vol 34 (1) ◽  
pp. 39-47 ◽  
Author(s):  
J. R. Blais
Keyword(s):  
Picea Glauca ◽  
Radial Growth ◽  
Choristoneura Fumiferana ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
White Spruce ◽  
Balsam Fir ◽  
First Year ◽  
Growth Ratio ◽  
Breast Height

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.

Foliage architecture explains oviposition preference of spruce budworm (Lepidoptera: Tortricidae) for white spruce over balsam fir

2006 ◽  
Vol 138 (2) ◽  
pp. 198-204 ◽  
Author(s):  
Gary G. Grant
Keyword(s):  
Picea Glauca ◽  
Choristoneura Fumiferana ◽  
Oviposition Preference ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
White Spruce ◽  
Spatial Arrangement ◽  
Balsam Fir

AbstractI conducted dual-choice oviposition bioassays to test the hypothesis that spruce budworm, Choristoneura fumiferana (Clemens), prefer the foliage architecture (spatial arrangement of foliage needles) of white spruce (Picea glauca (Moench) Voss; Pinaceae) to that of balsam fir (Abies balsamea (L.) P. Mill.; Pinaceae). Needles of white spruce radiate around the twig axis, giving the foliage a round architecture. Needles of balsam fir typically radiate bilaterally from the twig axis, giving the foliage a flat architecture, although on some trees foliage needles radiate around the twig axis, giving the foliage a round architecture. In bioassays, females showed a 2.4:1 preference for white spruce over "flat" balsam fir foliage, but this preference was reduced significantly to a 1.2:1 ratio when balsam fir had a round architecture. Given a choice between "round" and "flat" balsam fir foliage, females preferred the "round" foliage by a 2.2:1 margin. A similar preference for the round architecture was also observed when artificial (plastic) foliage with the two types of needle arrangements were compared. I conclude that the spatial arrangement of foliage needles is a major factor responsible for the oviposition preference of spruce budworm for white spruce over balsam fir.

Interactions among defoliation level, species, and soil richness determine foliage production during and after simulated spruce budworm attack

2020 ◽  
Vol 50 (6) ◽  
pp. 565-580
Author(s):  
Yuanyuan Wu ◽  
David A. MacLean ◽  
Chris Hennigar ◽  
Anthony R. Taylor
Keyword(s):  
Picea Glauca ◽  
Black Spruce ◽  
Choristoneura Fumiferana ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
White Spruce ◽  
Shoot Length ◽  
Balsam Fir ◽  
Site Quality ◽  
Number Of Shoots

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.

EFFICACY AND FIELD PERSISTENCE OF BACILLUS THURINGIENSIS AFTER GROUND APPLICATION TO BALSAM FIR AND WHITE SPRUCE IN WISCONSIN

1984 ◽  
Vol 116 (2) ◽  
pp. 153-158 ◽  
Author(s):  
R. C. Reardon ◽  
K. Haissig
Keyword(s):  
Bacillus Thuringiensis ◽  
Picea Glauca ◽  
Choristoneura Fumiferana ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
White Spruce ◽  
Balsam Fir

AbstractBacillus thuringiensis was applied at three dosages (1.0 BIU/tree, 0.1 BIU/tree, and.01 BIU/tree) to balsam fir, Abies balsamea (L.) Mill., and white spruce, Picea glauca (Moench) Voss, with mist blowers. Crystalline proteins were detected on balsam fir foliage for a maximum of 16 days (d) after B. thuringiensis was applied at 1.0 BIU/tree. Higher levels of crystalline proteins were detected on white spruce foliage treated with Thuricide 16B than on that treated with Dipel 4L. On balsam fir, the situation was the opposite. Mist-blower-treated foliage collected for up to 16 d posttreatment caused mortality of spruce budworm, Choristoneura fumiferana (Clemens), larvae. Viable endospores of B. thuringiensis were recovered on white spruce foliage collected 1 year after treatment.

WHITE SPRUCE AND THE SPRUCE BUDWORM: DEFINING THE PHENOLOGICAL WINDOW OF SUSCEPTIBILITY

1997 ◽  
Vol 129 (2) ◽  
pp. 291-318 ◽  
Author(s):  
Robert K. Lawrence ◽  
William J. Mattson ◽  
Robert A. Haack
Keyword(s):  
Picea Glauca ◽  
High Performance ◽  
Choristoneura Fumiferana ◽  
Spruce Budworm ◽  
White Spruce ◽  
Shoot Elongation ◽  
Larval Survival ◽  
Strongly Correlated ◽  
Negative Effect ◽  
Foliar Traits

AbstractSynchrony of insect and host tree phenologies has often been suggested as an important factor influencing the susceptibility of white spruce, Picea glauca (Moench) Voss, and other hosts to the spruce budworm, Choristoneura fumiferana (Clemens) (Lepidoptera: Tortricidae). We evaluated this hypothesis by caging several cohorts of spruce budworm larvae on three white spruce populations at different phenological stages of the host trees, and then comparing budworm performance with host phenology and variation of 13 foliar traits. The beginning of the phenological window of susceptibility in white spruce occurs several weeks prior to budbreak, and the end of the window is sharply defined by the end of shoot growth. Performance was high for the earliest budworm cohorts that we tested. These larvae began feeding 3–4 weeks prior to budbreak and completed their larval development prior to the end of shoot elongation. Optimal synchrony occurred when emergence preceded budbreak by about 2 weeks. Larval survival was greater than 60% for individuals starting development 1–3 weeks prior to budbreak, but decreased to less than 10% for those starting development 2 or more weeks after budbreak and thus completing development after shoot elongation ceased. High performance by the budworm was most strongly correlated with high levels of foliar nitrogen, phosphorous, potassium, copper, sugars, and water and low levels of foliar calcium, phenolics, and toughness. These results suggest that advancing the usual phenological window of white spruce (i.e. advancing budbreak prior to larval emergence) or retarding budworm phenology can have a large negative effect on the spruce budworm’s population dynamics.

LONG TERM STUDY OF THE EFFECTIVENESS OF AERIAL APPLICATION OF BACILLUS THURINGIENSIS – ACEPHATE COMBINATIONS AGAINST THE SPRUCE BUDWORM, CHORISTONEURA FUMIFERANA (LEPIDOPTERA: TORTRICIDAE)

1977 ◽  
Vol 109 (9) ◽  
pp. 1239-1248 ◽  
Author(s):  
O. N. Morris
Keyword(s):  
Bacillus Thuringiensis ◽  
Choristoneura Fumiferana ◽  
Larval Mortality ◽  
Abies Balsamea ◽  
Spruce Budworm ◽  
White Spruce ◽  
Balsam Fir ◽  
Population Densities ◽  
Long Term Study

AbstractBacillus thuringiensis (Dipel® 36B) mixed with a sublethal concentration of acephate (Orthene®) (O, S-dimethyl acetylphosphoramidothioate), an organophosphorous insecticide, was applied at 2.35–14 l./ha to white spruce (Picea glauca) and balsam fir (Abies balsamea) trees infested with spruce budworm, Choristoneura fumiferana (Clem.). The treatment rate was 20 Billion International Units of B. thuringiensis (B.t.) activity with or without 42 g of active ingredient of acephate/ha.The ground deposit of the standard Dipel wettable powder formulation was 12% of emitted volume compared with 21–32% for the Dipel 36B flowable. The viability of B.t. spores was drastically reduced after 1 day of weathering but a high level of biological activity by the spore–crystal complex persisted for up to 20 days post-spray due probably to crystal activity.The addition of about 10% of the recommended operational rate of acephate to the B.t. suspension increased larval mortality by 34% when applied at 4.7 l./ha. Reductions in budworm populations were 97–99% in B.t. + acephate plots and 86–90% in B.t. alone plots.Plots with moderate budworm densities of up to 27 larvae/100 buds on white spruce and 36/100 on balsam fir were satisfactorily protected from excessive defoliation in the year of spray by B.t. with or without acephate. Plots with higher population densities were not satisfactorily protected based on the branch sample examination but aerial color photographs indicated good protection to the top third of the trees. Population declines were greater and defoliation and oviposition were lower in the treated plots than in the untreated checks 1 year later without further treatment. Two years later the larval population densities in all plots were low but the density was twice as high in the untreated check as in the treated plots, indicating long term suppression by the treatments. Defoliation was negligible in all plots.The treatments had no deleterious effect on spruce budworm parasitism. The data indicate that the integrated approach using Bacillus thuringiensis – chemical pesticide combinations is a viable alternative to the use of chemical pesticides alone in spruce budworm control. Large scale testing is now warranted.

scholarly journals Genetic control and evolutionary potential of a constitutive resistance mechanism against the spruce budworm (Choristoneura fumiferana) in white spruce (Picea glauca)

Heredity ◽  
2018 ◽  
Vol 121 (2) ◽  
pp. 142-154 ◽  
Author(s):  
Claudia Méndez-Espinoza ◽  
Geneviève J. Parent ◽  
Patrick Lenz ◽  
André Rainville ◽  
Laurence Tremblay ◽  
...  
Keyword(s):  
Genetic Control ◽  
Picea Glauca ◽  
Choristoneura Fumiferana ◽  
Resistance Mechanism ◽  
Spruce Budworm ◽  
White Spruce ◽  
Evolutionary Potential ◽  
Constitutive Resistance

SOIL APPLICATION OF CARBOFURAN TO CONTROL SPRUCE BUDWORM, CHORISTONEURA FUMIFERANA (LEPIDOPTERA: TORTRICIDAE), IN A MANAGED WHITE SPRUCE SEED PRODUCTION AREA

1981 ◽  
Vol 113 (10) ◽  
pp. 949-951 ◽  
Author(s):  
W. H. Fogal ◽  
D. A. Winston ◽  
S. M. Lopushanski ◽  
D. A. MacLeod ◽  
A. J. Willcocks
Keyword(s):  
Seed Production ◽  
Picea Glauca ◽  
Choristoneura Fumiferana ◽  
Spruce Budworm ◽  
White Spruce ◽  
Cone Production ◽  
Seed Supply ◽  
Current Outbreak ◽  
Production Area ◽  
Production Areas

White spruce, Picea glauca (Moench) Voss, is a major commercial tree species used in reforestation programs throughout Canada, and seed requirements cannot be met in some years because of insect damage and the periodic nature of cone crops. The spruce budworm, Choristoneura fumiferana (Clem.), feeds on buds and cones of its hosts, causing a pronounced decrease in cone production (Schooley 1978). A current outbreak in northeastern Ontario poses a serious threat to white spruce seed supply from high value, managed seed production areas. Therefore, in 1979, we began an experiment to determine whether carbofuran, a systemic insecticide, could be used to protect buds and cones when applied to soil. We chose carbofuran because it has proved successful for control of some insects in seed orchards in the southeastern United States (DeBarr 1978)

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