Isozyme differences between the developmental stages of the parthenogenetic gall wasp Diplolepis rosae

The value of electrophoretic analysis of enzymes as an aid in connecting a morphologically deviating form to one of several possible species is dependent on the proportion of shared enzyme loci between the forms. In order to determine this proportion for the different instars of the parthenogenetic gall wasp Diplolepis rosae, 16 different enzyme systems were analysed. Out of the 37 loci detected, 25 (68%) were active in all instars. The larvae, pupae, and imagines had two, one and five unique loci, respectively. Larvae and pupae shared four loci not expressed in the imagines. In the ten enzymes analysed for comparison of males and females a total of 22 loci were detected, 21 found in both sexes and one unique to the females. The difference in isozyme pattern was found to be much more pronounced between pupa and imago than between larva and pupa. The chance to find a locus in an instar when already detected in another was calculated to 87%. If this estimate is valid for other forms within species, differential activity should not present a problem when electrophoretic analysis is used in order to connect such forms.