Reproductive behaviour of Ephestia Kuehniella Zeller (Lepidoptera: Pyradidae) : a thesis presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Entomology at Massey University, Palmerston North, New Zealand
dc.contributor.author | Xu, Jin | |
dc.date.accessioned | 2010-12-01T00:12:16Z | |
dc.date.available | NO_RESTRICTION | en_US |
dc.date.available | 2010-12-01T00:12:16Z | |
dc.date.issued | 2010 | |
dc.description | Content not included due to copyright restrictions: Appendix Published papers from PhD study Xu, J., & Wang, Q. (2010). Form and nature of precopulatory sexual selection in both sexes of a moth. Naturwissenschaften, 97(7), 617-625. Xu, J., & Wang, Q. (2010). Mechanisms of last male precedence in a moth: Sperm displacement at ejaculation and storage sites. Behavioral Ecology, 21(4), 714-721. Xu, J., & Wang, Q. (2010). Thiotepa, a reliable marker for sperm precedence measurement in a polyandrous moth. Journal of Insect Physiology, 56(1), 102-106. Xu, J., & Wang, Q. (2009). A polyandrous female moth discriminates against previous mates to gain genetic diversity. Animal Behaviour, 78(6), 1309-1315. Xu, J., & Wang, Q. (2009). Male moths undertake both pre- and in-copulation mate choice based on female age and weight. Behavioral Ecology and Sociobiology, 63(6), 801-808. Xu, J., Wang, Q., & He, X. Z. (2008). Emergence and reproductive rhythms of ephestia kuehniella (lepidoptera: Pyralidae). New Zealand Plant Protection, 61, 277-282. Xu, J., Wang, Q., & He, X. Z. (2007). Influence of larval density on biological fitness of ephestia kuehniella zeller (lepidoptera: Pyralidae). New Zealand Plant Protection, 60, 199-202. | en_US |
dc.description.abstract | Ephestia kuehniella is a pest of stored grain products. It also is widely used to rear parasitoids and predators. Prior to this study, little information was available on its reproductive behaviour. The fitness of E. kuehniella decreases with the increase of rearing density; a density of 100 larvae/50g food is recommended to produce high quality insects. Females emerge earlier than males. Emergence peaks at dusk; calling, courtship and mating peak in the late part of the 1st scotophase following emergence; oviposition peaks in the early part of the 2nd scotophase following emergence. Newly emerged virgin females carry <5 mature eggs, and the egg load increase to ≈240 three days after emergence and remains unchanged thereafter. Male accessory gland secretions stimulate egg maturation; mated females produce ≈300 mature eggs. Males produce two types of sperm, eupyrene (nucleate) and apyrene (anucleate) sperm. After mating, it takes 11 h for most eupyrene and apyrene sperm to reach the spermatheca. The presence of eupyrene sperm in the spermatheca is the main factor that elicits oviposition. The highest fecundity can be achieved when both sexes are 1-d-old at mating compared to older insects; delaying mating for 7 d reduces female fecundity by 60%. There is no significant effect of parental age on offspring fitness. Virgin females live longer than mated ones because the former allocate less resource for egg production. Larger females have higher fecundity and larger males produce larger spermatophores. Larger parents have larger sons and daughters. Females prefer large and mid-aged males for mating. Males prefer large, young and virgin females for mating. Males strategically adjust ejaculate size according to the degree of sperm competition risks. Both sexes mate multiply where males can copulate up to 9 times and females up to 4 times in their lifetime. Larger and younger females are more likely to remate. Multiple mating does not increase female fecundity, fertility and longevity. Females discriminate against previous mates and strategically adjust oviposition to gain genetic benefit via increasing offspring genetic diversity. Using a chemosterilant, thiotepa, I determined that the last male to mate with a female sires most of her offspring. The last male sperm precedence may be due to sperm displacement at both sperm ejaculation and storage sites, where the 2nd male physically displaces the 1st male’s spermatophore with his own in the bursa copulatrix and triggers the female to dump ≈50% resident sperm in the spermatheca. Spermathecal contractions appear to be the mechanism for sperm ejection. The outcome of sperm displacement is the result of male×female interactions. | en_US |
dc.identifier.uri | http://hdl.handle.net/10179/1931 | |
dc.language.iso | en | en_US |
dc.publisher | Massey University | en_US |
dc.rights | The Author | en_US |
dc.subject | Ephestia Kuehniella Zeller | en_US |
dc.subject | Lepidoptera | en_US |
dc.subject | Pyradidae | en_US |
dc.subject | Mediterranean flour moth | en_US |
dc.subject | Entomology | en_US |
dc.subject | Reproduction | en_US |
dc.subject.other | Fields of Research::270000 Biological Sciences::270500 Zoology::270505 Entomology | en_US |
dc.title | Reproductive behaviour of Ephestia Kuehniella Zeller (Lepidoptera: Pyradidae) : a thesis presented in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Entomology at Massey University, Palmerston North, New Zealand | en_US |
dc.type | Thesis | en_US |
massey.contributor.author | Xu, Jin | |
thesis.degree.discipline | Entomology | en_US |
thesis.degree.grantor | Massey University | en_US |
thesis.degree.level | Doctoral | en_US |
thesis.degree.name | Doctor of Philosophy (Ph.D.) | en_US |
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