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A COMPARISON OF DISCRIMINATION AND OF DENSITY RESPONSES DURING OVIPOSITION BY EXENTERUS AMICTORIUS AND E. DIPRIONIS (HYMENOPTERA: ICHNEUMONIDAE), PARASITES OF NEODIPRION SWAINEI (HYMENOPTERA: DIPRIONIDAE)

Published online by Cambridge University Press:  31 May 2012

J. M. McLeod
Affiliation:
Laurentian Forest Research Centre, Canadian Forestry Service, Quebec, Quebec

Abstract

The oviposition behavior of Exenterus amictorius Panzer, an introduced parasite of pre-spinning eonymphs of the Swaine jack pine sawfly, Neodiprion swainei Middleton, was studied in a series of field experiments over a 5-year period in the Province of Quebec. The ability of this parasite to discriminate against hosts with previously deposited progeny varied significantly: discrimination was lacking at the beginning of the host’s spinning period, but was rapidly acquired and persisted to the end of the spinning period. The relationships were described by negative power functions of the form Iδ = aX−b, where Iδ = Morisita’s Index of Dispersion, and X = the number of days from the beginning of the host’s spinning period. The response of E. amictorius to changing host densities, however, was positive at all host densities and described by functions of the form Y = aXb, where Y = number of parasite progeny per host and X = number of hosts dropping into funnel traps at 2-day intervals during the spinning period. Over 67% of the variation in the number of progeny deposited by E. amictorius during a field experiment in 1969 was explained by changes in adult parasite density, and an additional 19% by changes in host numbers. This indicates strongly that the observed change in discrimination against previously deposited progeny bears no direct relationship to either host or parasite density. It was suggested that the change might be influenced either by a reduction in the parasite’s egg complement in time, or by an associative learning process.

The density response of an indigenous parasite, Exenterus diprionis Rohwer, was comparatively much weaker and it seemed to lack the adaptive changes in discrimination against previously deposited progeny possessed by E. amictorius. Although attacks of the one species occurred independently of the other, in the event of multiparasitism E. amictorius always survived because of its faster rate of development in the host. The role of discrimination and of density response in the dominance of E. amictorius among the Exenterus spp. attacking N. swainei, and its successful establishment on a variety of North American diprionids, is discussed.

Résumé

Étude en une série d’expériences en forêt échelonnées sur cinq années au Québec du comportement au cours de la pondaison d’Exenterus amictorius Panzer, un parasite exotique de la Tenthrède de Swaine (Neodiprion swainei Middleton) au premier stade nymphal précédant la formation du cocon. Variation considérable de l’aptitude de ce parasite à sélectionner des hôtes déjà parasités, laquelle propriété fait défaut au seuil de la période de formation du cocon de l’hôte mais s’acquiert rapidement et dure jusqu’au terme de cette période. Description de ces relations par des fonctions à exposant négatif de la forme Iδ = aX−b, où Iδ représente le coefficient de dispersion de Morisita et X, le nombre de jours depuis le commencement de la période de formation du cocon de l’hôte. Réaction positive d’E. amictorius à tous les changements de densité chez l’hôte, décrite par des fonctions de la forme Y = aXb dans lesquelles Y = nombre de couvains du parasite par hôte et X = nombre d’hôtes tombant dans les pièges à entonnoir par intervalles de deux jours durant la formation du cocon. Plus de 67% de la variation numérique des couvains d’E. amictorius lors d’une expérience en forêt en 1969 s’expliquait par des changements numériques intervenus chez l’hôte, ce qui constitue un puissant indice que le changement observé relativement à la discrimination des couvains précédemment déposés ne comporte aucune relation directe avec la densité de l’hôte ou du parasite. On a suggéré qu’un tel changement pourrait être influencé soit par une réduction de la ponte avec le temps, soit par un processus associatif d’apprentissage.

La réaction d’un parasite indigène, Exenterus diprionis Rohwer, à la densité s’avérait comparativement plus faible et paraissait dépourvue des modifications adaptatives que possède E. amictorius dans la discrimination des couvains en place. Quoique les attaques de l’une et l’autre espèce eussent lieu indépendamment, en cas de multiparasitisme E. amictorius survivait toujours à cause de son rythme de développement plus rapide chez l’hôte. Discussion du rôle joué par la réaction à la discrimination et à la densité dans la dominance d’E. amictorius parmi les espèces d’Exenterus attaquant N. swainei, et de son succès à coloniser toute une variété de diprionidés d’Amérique du Nord.

Type
Articles
Copyright
Copyright © Entomological Society of Canada 1972

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References

Barclay, J. M. 1938. The oviposition habits of some species of the genus Exenterus parasitic on sawfly larvae. 69th A. Rep. ent. Soc. Ont. (1938): 2931.Google Scholar
Burnett, T. 1958 a. Effect of host distribution on the reproduction of Encarsia formosa Gahan (Hymenoptera: Chalcidoidea). Can. Ent. 90: 179191.CrossRefGoogle Scholar
Burnett, T. 1958 b. Effect of area of search on reproduction of Encarsia formosa Gahan (Hymenoptera: Chalcidoidea). Can. Ent. 90: 225229.CrossRefGoogle Scholar
Griffiths, K. J. 1969. The importance of coincidence in the functional and numerical response of two parasites of the European pine sawfly. Can. Ent. 101: 673713.CrossRefGoogle Scholar
Griffiths, K. J. and Holling, C. F.. 1969. A competition submodel for parasites and predators. Can. Ent. 101: 785818.CrossRefGoogle Scholar
Lyons, L. A. 1963. The European pine sawfly, Neodiprion sertifer (Geoff.) (Hymenoptera: Diprionidae). A review with emphasis on studies in Ontario. Proc. ent. Soc. Ont., 94: 537.Google Scholar
Mason, W. R. M. 1967. Specialization in the egg structure of Exenterus (Hymenoptera: Ichneumonidae) in relation to distribution and abundance. Can. Ent. 99: 375384.CrossRefGoogle Scholar
McGugan, B. M. and Coppel, H. C.. 1962. A review of the, biological control attempts against insects and weeds in Canada. Commonw. Agric. Bur. Tech. Commun. 2, p. 87, 106.Google Scholar
McLeod, J. M. 1966. An infestation of the jack pine sawfly (Neodiprion pratti banksianae Rah.) in Quebec. Bi-mon. Res. Notes, Can. Dep. Forest. and Rural Dev. 24(1): 56.Google Scholar
McLeod, J. M. and Desalliers, G.. 1966. Notes on Exenterus amictorius Panzer, an introduced parasite now established on Neodiprion swainei Middleton. Bi-mon. Prog. Rep. Can. Dep. Forest. 22(2): 2.Google Scholar
McLeod, J. M. and Smirnoff, W.. 1971. Neodiprion swainei Midd., Swaine jack-pine sawfly (Hymenoptera: Diprionidae). Commonw. Inst. biol. Control (Trinidad) Tech. Commun. NO. 4, p. 162167.Google Scholar
Mertins, J. W. and Coppel, H. C.. 1968. The changing role of Exenterus amictorius Panzer, a parasite of Diprion similis (Hartig) in Wisconsin. Univ. Wis. Res. Notes, No. 138.Google Scholar
Miller, C. A. 1959. The interaction of the spruce budworm, Choristoneura fumiferana (Clem.) and the parasite Apateles fumiferanae Vier. Can. Ent. 91: 457477.CrossRefGoogle Scholar
Morisita, M. 1962. Iδ index, a measure of dispersion of individuals. Researches Popul. Ecol. Kyoto Univ. 4: 17.Google Scholar
Pilon, J. G., Tripp, H. A., McLeod, J. M., and Illnytsky, S. L.. 1964. Influence of temperature of pre-spinning eonymphs of the Swaine jack pine sawfly, Neodiprion swainei Middleton (Hymenoptera: Diprionidae). Can. Ent. 96: 14501457.CrossRefGoogle Scholar
Price, P. W. and Tripp, H. A.. 1972. Activity patterns of parasitoids on the Swaine jack pine sawfly, Neodiprion swainei, and parasitoid impact on the host. Can. Ent. 104: 10031016.CrossRefGoogle Scholar
Reeks, W. A. 1952. Establishment of Exenterus spp. (Hymenoptera: Ichneumonidae), parasites of the European spruce sawfly, near points of introduction. Can. Ent. 84(3): 7686.CrossRefGoogle Scholar
Salt, G. 1934. Experimental studies in parasitism. II. Superparasitism. Proc. Roy. ent. Soc. Lond. (B) 117: 413435.Google Scholar
Thorpe, W. H. 1956. Learning and instinct in animals. Methuen. p. 221, 256.Google Scholar
Tripp, H. A. 1965. The development of Neodiprion swainei Middleton (Hymenoptera: Diprionidae) in the province of Quebec. Can. Ent. 97: 92107.CrossRefGoogle Scholar
Ullyett, G. C. 1949 a. Distribution of progeny by Chelonus texanus Cress. (Hymenoptera: Braconidae). Can. Ent. 81: 2544.CrossRefGoogle Scholar
Ullyett, G. C. 1949 b. Distribution of progeny by Cryptus inornatus Pratt (Hymenoptera: Ichneumonidae). Can. Ent. 81: 285299.CrossRefGoogle Scholar