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THE MATING STATUS OF FIELD-COLLECTED MALE SPRUCE BUDWORM, CHORISTONEURA FUMIFERANA (CLEM.) (LEPIDOPTERA: TORTRICIDAE), IN RELATION TO TRAP LOCATION, SAMPLING METHOD, SAMPLING DATE, AND ADULT EMERGENCE

Published online by Cambridge University Press:  31 May 2012

J.C. Bergh
Affiliation:
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
E.S. Eveleigh
Affiliation:
Canadian Forestry Service —Maritimes, PO Box 4000, Fredericton, New Bmnswick, Canada E3B 5P7
W.D. Seabrook
Affiliation:
Department of Biology, University of New Brunswick, Fredericton, New Brunswick, Canada E3B 6E1
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Abstract

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Male 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.

Résumé

Des papillons mâles de la tordeuse des bourgeons de l’épinette, Choristoneura fumiferana (Clem.), ont été piégés en 1986 et 1987, et la proportion des papillons récemment accouplés a été déterminée dans chaque échantillon. Le statut d’accouplement a été étudié en rapport avec le site de piégeage, la méthode d’échantillonnage, la date de l’échantillon, et l’émergence. Pour une date donnée, la proportion de mâles récemment accouplés était similaire entre pièges à phéromone, et ce aussi bien intra- qu’inter-site. Le nombre de mâles capturés augmentait avec l’élévation du site de capture, bien qu’il n’y avait pas de différence quant à la proportion des mâles accouplés. Des mâles montrant le comportement dit “de recherche ”d’une partenaire" ont été capturés au filet. On a trouvé qu’ils étaient accouplés dans les mêmes proportions que ceux capturés au piège à phéromone. La proportion des mâles récemment accouplés tendait à augmenter durant la première partie de la saison de vol, à fluctuer en mi-saison et ensuite à décroître en fin de saison. Ce patron était dû en partie aux fluctuations de l’émergence des adultes.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1988

References

Bergh, J.C., and Seabrook, W.D.. 1986 a. A simple technique for indexing the mating status of male spruce budworm. Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 118: 3741.CrossRefGoogle Scholar
Bergh, J.C., and Seabrook, W.D.. 1986 b. The mating status of spruce budworm males, Choristoneura fumiferana (Clem.) (Lepidoptera: Tortricidae). caught in pheromone-baited traps. J. Ent. Sci. 21: 254262.Google Scholar
Callahan, P.S., and Casio, T.. 1963. Histology of the reproductive tracts and transmission of sperm in the corn earworm, Heliothis zea. Ann. ent. Soc. Am. 56: 535556.CrossRefGoogle Scholar
Campbell, I.M. 1961. Polygyny in Choristoneura Led. (Lepidoptera: Tortricidae). Can. Ent. 93: 11601162.CrossRefGoogle Scholar
Fitzgerald, T.D., St. Clair, A.D., Daterman, G.E., and Smith, R.G.. 1973. Slow release plastic formulation of the cabbage looper pheromone, cis-7-dodecenyl acetate: release rates and biological activity. Environ. Ent. 2: 607610.CrossRefGoogle Scholar
Haines, L.C. 1981. Changes in colour of a secretion in the reproductive tract of adult males of Spodoptera littoralis (Boisduval) (Lepidoptera: Noctuidae) with age and mated status. Bull. ent. Res. 71: 591598.CrossRefGoogle Scholar
Henneberry, T.C., and Clayton, T.E.. 1984. Time of emergence, mating, sperm movement, and transfer of ejaculatory duct secretory fluid by Heliothis virescens (F.) (Lepidoptera: Noctuidae) under reversed lightdark cycle laboratory conditions. Ann. ent. Soc. Am. 77: 301305.CrossRefGoogle Scholar
Houseweart, M.W., Jennings, D.T., and Sanders, C.J.. 1981. Variables associated with pheromone traps for monitoring spruce budworm populations (Lepidoptera: Tortricidae). Can. Ent. 113: 527537.CrossRefGoogle Scholar
Outram, I. 1970. Recognition of mated male spruce budworm moths. Can. Fish. For. Bi-mon. Res. Notes 26: 3.Google Scholar
Outram, I. 1971. Aspects of mating in the spruce budworm, Choristoneura fumiferana (Lepidoptera: Torticidae). Can. Ent. 103: 11211128.CrossRefGoogle Scholar
Sanders, C.J. 1975. Factors affecting adult emergence and mating behaviour of the eastern spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 107: 967977.CrossRefGoogle Scholar
Sanders, C.J. 1981. Release rates and attraction of PVC lures containing synthetic sex attractant of the spruce budworm, Choristoneura fumiferana (Lepidoptera: Tortricidae). Can. Ent. 113: 103111.CrossRefGoogle Scholar
Sanders, C.J., and Weatherston, J.. 1976. Sex pheromone of the eastern spruce budworm (Lepidoptera: Tortricidae): optimum blend of trans- and cis-11-tetradecenal. Can. Ent. 108: 12851290.CrossRefGoogle Scholar
Silk, P.J., Tan, S.H., Weisner, C.J., Ross, R.J., and Lonergan, G.C.. 1980. Sex pheromone chemistry of the eastern spruce budworm, Choristoneura fumiferana. Environ. Ent. 9: 640644.CrossRefGoogle Scholar
Smith, S.G. 1954. A partial breakdown of temporal and ecological isolation between Choristoneura species (Leipdoptera: Tortricidae). Evolution 8: 206224.CrossRefGoogle Scholar
Snow, J.W., and Carlysle, T.C.. 1967. A characteristic indicating the mating status of male fall armyworm moths. Ann. ent. Soc. Am. 60: 10711074.CrossRefGoogle Scholar
Sokal, R.R., and Rohlf, F.J.. 1969. Biometry. W.H. Freeman and Co., San Francisco. 776 pp.Google Scholar
Zar, J.H. 1984. Biostatistical Analysis, 2nd ed. Prentice-Hall, Inc. 718 pp.Google Scholar