EFFECTS OF SYNTHETIC JUVENILE HORMONE ON ADULT EMERGENCE AND REPRODUCTION OF THE FEMALE SPRUCE BUDWORM, CHORISTONEURA FUMIFERANA (LEPIDOPTERA: TORTRICIDAE)

1972 ◽  
Vol 104 (2) ◽  
pp. 271-273 ◽  
Author(s):  
I. Outram
1975 ◽  
Vol 107 (9) ◽  
pp. 967-977 ◽  
Author(s):  
C. J. Sanders

AbstractLaboratory and field experiments indicate that the female spruce budworm (Choristoneura fumiferana (Clem.)) pupal stadium requires approximately 122C degree-days above a threshold of 7.2 °C (45°F), the male 124. Emergence time on any given day depends on temperature but is independent of photoperiod. Under field conditions male and female budworm mate only once per 24-h period. In the laboratory under continuous illumination females mate repeatedly and males readily mate a second time within a few hours, but the duration of the second copulation is abnormally long. The probability of multiple matings under field conditions is reduced by the restricted period of sexual activity coupled with the duration of copulation and the lower competitiveness of mated insects. Antennae are essential to the male for successful copulation.


Forests ◽  
2019 ◽  
Vol 10 (9) ◽  
pp. 748 ◽  
Author(s):  
Jacques Régnière ◽  
Barry Cooke ◽  
Ariane Béchard ◽  
Alain Dupont ◽  
Pierre Therrien

Management of spruce budworm, Choristoneura fumiferana (Clem.), outbreak spread requires understanding the demographic processes occurring in low, but rising populations. For the first time, detailed observations were made in the early stages of outbreak development. We sampled populations over a three-year period in both treated and untreated populations in the Lower St-Lawrence region of Quebec, Canada, and measured the density-dependence of survival and population growth rates, and the impact of natural enemies and insecticides. Insecticides tested were Bacillus thuringiensis (Berliner 1915) and tebufenozide. We recorded strong density-dependence of survival between early larval stages and adult emergence, explained largely by the variation of natural enemy impacts and overcrowding. We also observed inverse density-dependence of apparent fecundity: net immigration into lower-density populations and net emigration from the higher, linked to a threshold of ~25% defoliation. Because of high migration rates, none of the 2013 treatments reduced egg populations at the end of summer. However lower migration activity in 2014 allowed population growth to be reduced in treated plots. This evidence lends support to the conclusion that, for a budworm population to increase to outbreak density, it must be elevated via external perturbations, such as immigration, above a threshold density of ~4 larvae per branch tip (L4). Once a population has increased beyond this threshold, it can continue growing and itself become a source of further spread by moth migration. These findings imply that populations can be brought down by insecticide applications to a density where mortality from natural enemies can keep the reduced population in check, barring subsequent immigration. While we recognize that other factors may occasionally cause a population to exceed the Allee threshold and reach outbreak level, the preponderance of immigration implies that if all potential sources of significant numbers of moths are reduced on a regional scale by insecticide applications, a widespread outbreak can be prevented, stopped or slowed down by reducing the supply of migrating moths.


1960 ◽  
Vol 92 (11) ◽  
pp. 839-850 ◽  
Author(s):  
C. A. Miller

This is the second of a series of papers (Miller, 1959) describing the interaction of primary parasites and the spruce budworm, Choristoneura fumiferana (Clem.), based on data collected during an outbreak of the budworm in northern New Brunswick during the period 1947–1958. The first paper showed that the interaction between the spruce budworm and Apanteles fumiferanae Vier. is adequately described by the general mathematicai model developed by Watt (1959). The data on the parasite Glypta fumiferanae (Vier.) to be presented in this paper are also analysed by means of Watt's model and consequently the method is essentially the same. There is, however, one important difference. In the case of A. fumiferanae, the estimated number of adult parasites was only an index based on the potential number emerging from the previous host generation. The observed density of G. fumiferanae is a more realistic estimate. It is based on the actual number of cocoons found on the foliage during the adult emergence period.


1988 ◽  
Vol 120 (8-9) ◽  
pp. 821-830 ◽  
Author(s):  
J.C. Bergh ◽  
E.S. Eveleigh ◽  
W.D. Seabrook

AbstractMale spruce budworm moths, Choristoneura fumiferana (Clem.), were captured in 1986 and 1987 and the proportion recently mated was determined for each sample. Mating status was examined in relation to trap location, sampling method, sampling date, and adult emergence. On a given day the proportion of recently mated males captured was similar among pheromone-baited traps both within and among test sites. The number of males trapped increased with increasing trap elevation, although there was no difference in the proportion of mated males at each elevation. Males exhibiting “mate-location behaviour” were captured individually with an insect net and were found to be mated in the same proportion as those caught in pheromone-baited traps. The proportion of recently mated males trapped tended to increase during the early part of the flight season, to fluctuate during the middle portion, and then to decline toward the end of the season. This pattern was due, in part, to adult emergence trends.


Forests ◽  
2020 ◽  
Vol 11 (6) ◽  
pp. 659 ◽  
Author(s):  
Dan Quiring ◽  
Greg Adams ◽  
Andrew McCartney ◽  
Sara Edwards ◽  
J. David Miller

Wild eastern spruce budworm (Choristoneura fumiferana Clemens) were reared on white spruce (Picea glauca (Moench) Voss) trees, half of which had been previously inoculated with a native endophytic fungus, Phialocephala scopiformis DAOM 229536 Kowalski and Kehr (Helotiales, Ascomycota). Survival up to pupation and up to adult emergence was approximately 27% higher for budworm juveniles that developed on control trees compared to trees inoculated with the endophyte. The endophyte did not influence the size or sex of survivors but did reduce defoliation by approximately 30%. Reductions in defoliation on endophyte-inoculated versus control trees, due to reductions in survival of juvenile budworms, suggests that tree inoculations with P. scopiformis could play an important role in integrated management programs against the eastern spruce budworm.


1989 ◽  
Vol 121 (12) ◽  
pp. 1111-1116 ◽  
Author(s):  
Hemendra Mulye ◽  
Roger Gordon

AbstractThe effectiveness of seven insect juvenile hormone analogs (JHAs) in disrupting metamorphosis of the eastern spruce budworm, Choristoneura fumiferana Clemens, was determined by applying the compounds topically to early sixth-instar larvae and monitoring subsequent development. Fenoxycarb showed promising control potential, with an LC50 of 0.26 μg per insect. Relative lethal effectiveness, based on LC50 values, was Fenoxycarb > ZR9892 > ZR8487 > S-71639 > methoprene > ZR9582 > ZR10151. Some of the JHAs tested may be useful in an integrated spruce budworm control program.


2000 ◽  
Vol 132 (3) ◽  
pp. 341-343 ◽  
Author(s):  
Kees van Frankenhuyzen ◽  
John Dedes

A process-oriented model was recently developed to simulate the efficacy of spray products containing Bacillus thuringiensis Berliner subsp. kurstaki (Bacillaceae) against the spruce budworm, Choristoneura fumiferana Clemens (Cooke and Régnière 1996). The model accurately predicted foliage protection and larval population reduction during validation spray trials (Régnière and Cooke 1998; Cooke and Régnière 1999). The impact of treatment on budworm generation survival was generally well mimicked by the model except for a consistent overestimation of survival at the end of immature development in the treated plots. Régnière and Cooke (1998) speculated that residual mortality due to treatment may be occurring during the pupal stage. Carry-over of B. thuringiensis from larvae to pupae has been documented for spruce budworm (Klein and Lewis 1966) and several other Lepidoptera (Legner and Oatman 1962; Angus 1965). Although we recently investigated the response of spruce budworm larvae to ingestion of sublethal doses of B. thuringiensis (Pedersen et al. 1997), effects on pupal survival or adult emergence were not examined. In this note, we report the results of an experiment designed to assess such effects.


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