MORPHOGENETIC EFFECTS OF AN INHIBITOR OF CUTICLE DEVELOPMENT ON THE SPRUCE BUDWORM, CHORISTONEURA FUMIFERANA (LEPIDOPTERA: TORTRICIDAE)

1975 ◽  
Vol 107 (8) ◽  
pp. 883-886 ◽  
Author(s):  
Arthur Retnakaran ◽  
Larry Smith

Abstract1-(4-chlorophenyl)-3-(2,6-difluorobenzoyl)-urea when ingested by the last two larval instars of the spruce budworm, Choristoneura fumiferana, inhibits cuticle development leading to morphogenetic deformities in the pupal stage. Laboratory and greenhouse studies indicate that this material could be used to control natural populations of spruce budworm.

2016 ◽  
Vol 149 (2) ◽  
pp. 227-240 ◽  
Author(s):  
Kees van Frankenhuyzen ◽  
Jacques Régnière

AbstractAerial application of Mimic® 2LV to rising outbreak populations of the spruce budworm (Choristoneura fumiferana (Clemens); Lepidoptera: Tortricidae) in Québec, Canada, resulted in high levels of population reduction at spray deposits of 0.5–1.2 μg tebufenozide/g of foliage. Application to potted host trees in outdoor enclosures followed by bioassays revealed multiple effects on spruce budworm survival and recruitment. Chronic (14-day) exposure of late-instars to treated foliage reduced larval survival and also pupal survival, mating success, and fecundity, depending on the product concentration applied. Treatments that produced foliar deposits of ~ 0.5–1.5 μg tebufenozide/g caused high larval mortality. Exposure to deposits of ~ 0.15–0.5 μg/g caused delayed mortality during the pupal stage and reduced the mating success of survivors, while exposure to ~ 0.07–0.15 μg/g reduced the fecundity of mated females. Sublethal exposure did not affect the progeny of survivors, either in egg hatch, survival during diapause, or survival and performance after diapause. Reduced survival during late-larval and pupal stages combined with lower recruitment as a result of reduced mating success and fecundity are likely to play a role in the suppression of Mimic®-treated spruce budworm populations in the years following treatment.


1984 ◽  
Vol 116 (2) ◽  
pp. 285-287
Author(s):  
Jean R. Finney ◽  
Gordon F. Bennett

Finney et al. (1982) reported on the susceptibility of the 4th to 6th larval instars and pupae of Choristoneura fumiferana (Clemens) to Heterorhabditis heliothidis (Khan, Brooks and Hirschmann). This report describes the susceptibility of the first three larval instars to the nematode. First-instar larvae search for suitable sites where they spin hibernacula in which they molt and overwinter as second-instar larvae. Most third-instar larvae burrow within the balsam fir buds. All these stages occupy cryptic habitats to which delivery of chemical pesticides is a problem. Rhabditid nematodes, which can actively seek out a target insect, may prove a more useful control agent under these circumstances.


1998 ◽  
Vol 130 (2) ◽  
pp. 215-229 ◽  
Author(s):  
Jeffrey G. Fidgen ◽  
Eldon S. Eveleigh

AbstractWe carried out a 2-year study to elucidate the biology of the gregarious, idiobiont ectoparasitoid Elachertus cacoeciae (Howard) by placing (implanting) laboratory-reared spruce budworm larvae [Choristoneura fumiferana (Clemens)] on current-year balsam fir (Abies balsamea L.) shoots in the field, simulating low (endemic) densities of the budworm. Spring female E. cacoeciae attacked fourth-, fifth-, and sixth-instar budworm larvae, beginning near the predicted peak of the fourth instar and ending about 10–12 days after the predicted peak of the pupal stage of the wild budworm population. The mean (±SE) brood size of spring females was 2.9 ± 0.3 E. cacoeciae pupae per host. The proportion of females increased during the season, with many broods consisting of 100% females late in the season. In 1994 and 1995, the mean proportion of females was 0.74 ± 0.05 and 0.79 ± 0.05, respectively. In the laboratory, development time from eggs to adults was approximately 20 days at 20.6 °C. Adult males provided with honey water lived 43.6 ± 3.2 days, whereas females provided with hosts and honey water lived 90.1 ± 6.6 days. Spring females had a pre-oviposition period of 11.5 ± 1.3 days, resulting in a generation time (egg to egg) of ~31 days. The oviposition period lasted 76.3 ± 7.7 days during which time spring females parasitized 19.2 ± 1.9 hosts, and produced a clutch size of 4.9 ± 0.4 eggs per host, for a lifetime fecundity of 96.8 ± 14.7 eggs. The post-oviposition period was 18.5 ± 3.7 days. Throughout their lifetime, spring females host fed only (host feeding without oviposition) on an additional 9.3 ± 1.9 hosts. Approximately 2% of pupae developing from spring females overwintered, whereas approximately 95% of pupae developing from summer females overwintered. Laboratory results for summer females suggest that they may be adapted to parasitizing alternate host(s) rather than spruce budworm.


1954 ◽  
Vol 86 (10) ◽  
pp. 439-454 ◽  
Author(s):  
Blair M. McGugan

Many of the early papers on the spruce budworm, Choristoneura fumiferana (Clem.), included accounts of the general habits and seasonal history of the insect (9, 13, 18, 10, 22). Later papers have heen concerned principally with ecological or pathological relations, current infestations and damage, or chemical control. There has not been, however, any detailed account of the salient features of the development of the spruce budworm.


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.


1958 ◽  
Vol 36 (3) ◽  
pp. 309-316 ◽  
Author(s):  
H. M. Thomson

Limited tests indicate that the microsporidian parasite Perezia fumiferanae is restricted to insect hosts of the genus Choristoneura and for practical purposes to the single species Choristoneura fumiferana (Clem.). Frozen spores of this parasite were found to be infectious longer than those kept under other conditions but no spores were infectious after 6 months' storage. There are two distinct methods of infection, oral and congenital. Immature eggs within infected female insects are infected by schizonts which develop into spores after the eggs are laid. All infected females, regardless of the degree of infection, transmit the parasite to their offspring, and for practical purposes all the progeny of such females are infected. Offspring of heavily infected females appear to contain more spores than those of lightly infected females. Infected males are sometimes capable of transmitting the parasite to a portion of their offspring. Congenital transmission is responsible for the passage of the parasite from host generation to generation. Increase in the incidence of the parasite occurs by oral ingestion of spores but the habits of the host larvae restrict most transmission to the late larval instars.


1984 ◽  
Vol 116 (2) ◽  
pp. 131-137 ◽  
Author(s):  
Paul G. Fast ◽  
John B. Dimond

AbstractDiet incorporation assays detected no difference in susceptibility of instars IV, V, and VI of spruce budworm exposed to Bacillus thuringiensis, either in terms of dose, LC50, or time, LT50. The hypothesis that the dose–response for larvae of each instar fitted a common regression line was statistically acceptable. Differences in the pattern of changes in larval weight of instars IV, V, VI larvae in response to dose were not detected.Small plots were sprayed with 5.5, 10.9, 21.9 BIU/ha at times corresponding to peak instar III, early IV, peak IV, peak V, and peak VI. Instar III larvae were controlled less effectively than were instar IV or V larvae which were controlled equally well. Instar VI larvae were also less effectively controlled than instar IV and V larvae probably because a significant proportion had reached the non-feeding prepupal stage before the full effect of B.t. was obtained.


2015 ◽  
Vol 148 (2) ◽  
pp. 163-170
Author(s):  
Kees van Frankenhuyzen ◽  
Yuehong Liu

AbstractInfection by Nosema fumiferanae (Thomson) (Microsporidia: Nosematidae) and feeding by late-instars on previous year’s foliage due to depletion of current year’s growth (also known as back-feeding) are likely to co-occur in high-density outbreak populations of the spruce budworm (Choristoneura fumiferana (Clemens) (Lepidoptera: Tortricidae)). We tested the hypothesis that effects of the two factors on larval fitness are exacerbated by their interaction. Twigs of balsam fir (Abies balsamea Linnaeus; Pinaceae) with or without new-growth shoots were fed to sixth-instar offspring from uninfected, moderately infected, or highly infected females in two laboratory experiments. Pupal mass and time to reach the pupal stage were significantly affected by infection and back-feeding but not by their interaction. Pupal mass decreased and development time increased with increasing spore burden in a linear fashion. Back-feeding had a significant effect on survival to the pupal stage, but infection did not, nor did their interaction. The relatively small changes in survival, pupal mass, and development time caused by infection and back-feeding were additive. The results thus refute our hypothesis that infection by N. fumiferanae and forced feeding on last year’s foliage by late instars are likely to interact in affecting spruce budworm recruitment in older outbreak populations.


1980 ◽  
Vol 112 (5) ◽  
pp. 443-450 ◽  
Author(s):  
Gary B. Dunphy ◽  
Richard A. Nolan

AbstractFive types of hemocytes (plasmatocytes, granular cells, spherule cells, oenocytoids, and prohemocytes) were identified in the larval, prepupal, and pupal stages of the spruce budworm, Choristoneura fumiferana (Clem.). Hemocyte numbers (total hemocyte counts and absolute hemocyte counts) increased during larval development. The absolute counts were greater in female larvae than in the male larvae during the fourth instar but were higher in the males during the fifth and sixth instars. Hemocyte numbers peaked in the prepupal stage in females and in the early pupal stage in males. The plasmatocytes and granular cells were the predominant hemocytes in both sexes. The plasmatocytes decreased and the granular cells increased throughout larval development of both sexes. There were more plasmatocytes in the males than in the females in all stages of development. There were more granular cells in the males than the females until the sixth instar when the reverse occurred.


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