Abstract

Though extra instars are often associated with poor conditions and thought to be a compensation for a low growth rate, the reasons why they are necessary, and for variable instar number existing under standard rearing conditions, are not yet clear. In standard rearing conditions, approximately half of Pseudocoremia suavis larvae had five instars (Type I larvae), and half six instars (Type II larvae). Type II larvae took longer to pupate and reached higher pupal weights than Type I larvae. The extra instar was not related to sexual size dimorphism; Type II larvae were not more likely to be females. Females of both Types pupated later than males and had higher pupal weights; this weight gain was achieved wholly via an extended final instar. Relative growth rates (RGR), instar durations and larval weights on weigh days were otherwise the same for both sexes. For most of the larval period, Type II larvae had lower RGR and lower weights than Type I larvae. They also had shorter 3 rd , 4 th and 5 th instars than Type I larvae, and the estimated weights at each moult were significantly lower. The Types are discussed in terms of being, in species with weight thresholds for pupation, not optional strategies involving different critical weight ratios for larval moults, but as an inevitable consequence of physiological timing con- straints upon reaching the critical weights for larval moults causing large variation in size after the moult. Small larvae may then need an extra instar to reach pupation. When parasitised in the second instar by Meteorus pulchricornis, P. suavis larvae produced parasitoids in either their fourth (4 th instar emerging (IE)) or fifth instar (5 th IE). The estimated moulting weights at each instar of 4 th IE and 5 th IE hosts were very similar to those of Type I and Type II unparasitised larvae respectively, which, together with similarity of instar dura- tion patterns, is strongly suggestive of Types being present within parasitised larvae. The proportion of 5 th IE hosts in the much slower- growing parasitised treatment was greater than the proportion of Type II larvae in the unparasitised treatment, as might be expected if Type II is associated with lower RGR. The lack of further Types appearing is consistent with extra instars being a compensation for small weight after the moult rather than low RGR per se.

Highlights

  • Within-species variability in instar number is not uncommon in insects and is widespread over insect taxa, being present in at least 145 species in 12 orders (Esperk et al, 2007a)

  • Pupal weight and development time of the geometrid Pseudocoremia suavis (Butler), which has been observed to undergo five or six larval instars under standard rearing conditions, to determine whether having six instars was related to sexual size dimorphism (SSD), or to having lower growth rates and taking longer to reach the same pupal weight as larvae with five instars

  • Under parasitism the growth rate was expected to be much reduced, and we investigated whether instar duration and estimated weights at moulting changed under the parasitism-mediated reduction in relative growth rate (RGR)

Read more

Summary

Introduction

Within-species variability in instar number is not uncommon in insects and is widespread over insect taxa, being present in at least 145 species in 12 orders (Esperk et al, 2007a). Esperk et al (2007a) review the phenomenon, and in such species the most common factors associated with a change in instar number are sexual size dimorphism (SSD), inheritance, and environmental factors such as photoperiod, temperature, humidity, and the quality and quantity of food. While gender may predispose a larva to have an extra instar to enable females to achieve a high degree of sexual size dimorphism (Esperk & Tammaru, 2006; Esperk et al, 2007b), environmental conditions associated with extra instars are usually adverse ones causing lower growth rates and smaller individuals. Manipulating an environmental condition for the worse often causes an increase in the proportion of larvae exhibiting a higher number of instars (Morita & Tojo, 1985; Casimero et al, 2000; Jensen & Cameron, 2004; Gould et al, 2005), suggesting that individuals are genetically capable of exhibiting either phenotype. The ability to add instars may allow a minimum pupal size to be reached in varying environmental conditions (Etile & Despland, 2008) or under varying growth rates associated with a wide host plant range (Casimero et al, 2000)

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call