Hostname: page-component-586b7cd67f-dsjbd Total loading time: 0 Render date: 2024-11-22T20:01:58.641Z Has data issue: false hasContentIssue false

The relationship between larval critical weight, latent feeding period and diet quality in the larval metamorphosis of Cnephasia Jactatana (walker) (Lepidoptera: Tortricidae)

Published online by Cambridge University Press:  19 September 2011

J. P. R. Ochieng-Odero
Affiliation:
Zoology Department, University of Auckland, Private Bag, Auckland, New Zealand
Get access

Abstract

The lowest weight at which a final instar larva of the leafroller, Cnephasia jactalana (Walker) (Lepidoptera: Tortricidae) can initiate pupation, the larval critical weight, was unaffected by diet quality. Use of a non-nutritive artificial diet showed that the larval-pupal metamorphosis was possibly triggered by stretch receptors, and was not related to nutrition per se. However, a final-instar larva was not able to moult until it had ingested and assimilated the quantity of food required to attain the larval critical weight. The period between attaining the larval critical weight and the larval maximum weight is the latent feeding period which was found to be longer on higher-quality diets. The decrease from larval maximum weight to pupal weight depended on diet quality: optimum-quality diets gave the smallest decreases. The decrease from pupal to adult weight was not affected by diet. Reproductive performance was strongly affected by the quality of the diet during the latent feeding period.

Résumé

Le poids minimal auquel le dernier stade de la larve de Cnephasia jactatana (Walker) (Lepidoptera: Tortricidae) initie la pupation, le poids critique de la larve, n'a pas ete influence par la qualite de l'alimentation. L'utilisation d'un regime alimentaire artificiel non nutritif a montre que la metamorphose larve-pupe serait declanchee par l'expansion des recepteurs et ne serait pas done pas liee a l'alimentation en tant que telle. Toutefois, le dernier stade larvaire n'a pu se metamorphoser qu'apres avoir ingère la quantite d'aliments necessaire pour atteindre le poids critique de la larve. La periode entre le poids critique et le poids maximal de la larve est dite periode latente de nutrition; celle-ci a ete plus longue lorsque la larve a ete soumise a des reqimes alimentaires de grande valeur nutritive. La baisse du poids maximal de la larve par rapport au poids de la pupe depend de la qualite du regime alimentaire. Les baisses en poids les plus legeres ont ete obtenues avec des milieux nutritifs de qualite optimale. La baisse en poids de la pupe par rapport a celle de l'adulte n'a pas ete influencee par la qualite de l'alimentation par contre la reproduction a ete serieusement affectee par la qualite de la nourriture pendant la periode latente de nutrition.

Type
Research Artilces
Copyright
Copyright © ICIPE 1993

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

Anwyl, R. (1972) The structure and properties of an abdominal stretch receptor in Rhodnius prolixus. J. Insect Physiol. 18, 21432153.CrossRefGoogle Scholar
Beckel, E. and Friend, W. G. (1964) The relation of abdominal distension and nutrition to moulting in Rhodnius prolixus (Stahl) (Hemiptera). Can. J. Zool. 42, 7181.CrossRefGoogle Scholar
Bhaskaran, G., Jones, G. and Jones, D. (1980) Neuroendocrine regulation of corpus allatum activity in Manduca sexta: Sequential neurohormonal and nervous inhibition in the last - instar larva. Proc. Nat. Acad. Sci. 77, 44074411.CrossRefGoogle ScholarPubMed
Ciemior, K. E., Sehnal, F., and Schneiderman, H. A. (1979) Moulting, growth and survival of Galleria mellonella L. (Lep., Pyralidae) treated with juveniods. J. Appi Entomol. 88, 414425.Google Scholar
Dadd, R. H. (1985) Nutrition: organisms. In Comprehensive Insect Biochemistry and Pharmacology Regulation: Digestion, Nutrition, Excretion Vol. IV, (Edited by Kerkut, G. A. and Gilbert, L. I.), Pergamon Press, Oxford, pp. 313390.CrossRefGoogle Scholar
Hagen, K. S., Dadd, R. H. and Reese, J. (1984) The food of insects. In Ecological Entomology (Edited by Huffaker, C. B. and Rabb, R. L.) John Wiley and Sons, New York. pp. 79112.Google Scholar
Keely, L. L. (1972) Neuroendocrine regulation of insect metabolism and the influence of nutrition. In Insect and Mite Nutrition (Edited by Rodriguez, J. G.), Elsevier, Amsterdam, pp. 541554.Google Scholar
Rester, K. M. and Smith, M. (1984) Effects of diet on the growth, fecundity and duration of tethered flight of Nezara viridula. Entomol. exp. Appi. 35, 7581.Google Scholar
Nijhout, H. F. (1979) Stretch-induced moulting in Oncopeltus fasciatus. J. Insect Physiol. 25, 277281.CrossRefGoogle Scholar
Nijhout, H. F. (1981) Physiological control of moulting in insects. Am. Zool. 21, 631640.CrossRefGoogle Scholar
Ochieng'-Odero, J. P. R. (1980) Critical, pupal and adult weights in the size related metamorphosis of the black Lyre leafroller Cnephasia jactatana. Entomol. exp. Appi. 54, 2127.CrossRefGoogle Scholar
Reinecke, J. P. (1985) Nutrition: artificial diets. In Comprehensive Insect Biochemistry and Pharmacology, Regulation: Digestion, Nutrition, Excretion, Vol. IV (Edited by Kerkut, G. A. and Gilbert, L. I.), Pergamon Press, Oxford, pp. 391419.CrossRefGoogle Scholar
Ryan, B. F., Joiner, B. L. and Ryan, T. A. Jr (1985) Minitab Handbk. Boston, Duxbury Press.Google Scholar
Sehnal, F. (1976) Action of juvenoids on different groups of insects. In The Juvenile Hormones (Edited by Gilbert, L. I.), Plenum Press, New York. pp. 301322.CrossRefGoogle Scholar
Singh, P. (1983) A general purpose laboratory diet mixture for rearing insects. Insect Sci. Applic. 4, 357362.Google Scholar
Slanky, F. Jr and Scriber, J. M. (1985) Food consumption and utilization. In Comprehensive Insect Biochemistry and Pharmacology Regulation: Di gestion, Nutrition, Excretion, Vol. IV (Edited by Kerkut, G. A. and Gilbert, L. I.), Pergamon Press, Oxford, pp. 271282.Google Scholar
Slama, K. (1975) Some old concepts and new findings on hormonal control of insect morphogenesis J. Insect Physio. 21, 921955.CrossRefGoogle Scholar
Thomas, W. P. (1986) An artificial diet for rearing the lightbrown apple moth Epiphyas postivittana (Walk) (Lepidoptera: Tortricidae). New Zealand J. Entomol. 4, 3132.CrossRefGoogle Scholar
Vanderzant, E. S. (1974) Development, significance, and application of artificial diets for insects. Ann. Rev. Entomol. 19, 139160.CrossRefGoogle Scholar
Wigglesworth, V. B. (1934) The physiology of ecdysis in Rhodnis prolixus (Hemiptera). II. Factors controlling moulting and “metamorphosis”. Q. J. Microsc. Sci. 77, 191222.Google Scholar
Ziegler, R. (1985) Metabolic energy expenditure and its hormonal regulation. In Environmental Physiology and Biochemistry of Insects (Edited by Hoffmann, K. H.), Springer-Verlag, Berlin. pp. 95118.Google Scholar