Morphological variation and life cycle category were examined in 121 clones of Myzus persicae (Sulzer). The clones were collected from tobacco from three localities in Greece (Xanthi, Nea Efessos and Naphplion), one in Germany (Rheinstetten), one in France (Bergerac) and one in Spain (Madrid). Before morphometrics, all aphids were laboratory-reared on potato. The morphological variation was investigated using both canonical variates analysis and a novel non-parametric classification tree method. The life cycle category was examined by rearing the clones for three generations under short day conditions. In Nea Efessos a relative high proportion of clones was found to overwinter as eggs on the primary host. In the other regions all collected clones were non-holocyclic. Intermediate genotypes were found in all regions at percentages ranging from 4.0 to 24.0%. Androcyclic clones were found only in Xanthi, Greece (4.0%) and Rheinstetten, Germany (16.7%). The canonical variates analysis and the tree classification method revealed important intrapopulation polymorphisms in clones from Bergerac, Nea Efessos and Madrid. Both methods separated the populations originating from Greece from those collected elsewhere in western Europe. The observed morphological variation was probably due to genetic differences, since all clones were reared in a common environment. The results are discussed in relation to factors responsible for genetic divergence in M. persicae populations.
Abstract. Male production was examined in 70 Myzus persicae s.str and M. persicae nicotianae clonal lineages at 17°C and 10L : 14D. Sixty nine were characterised by a partial loss of sexuality (androcyclic producing few males, and intermediates producing some males and mating females), and one was found to be permanently parthenogenetic. High within and between lineage variation was detected. Most (81%) of the clonal lineages produced few males (0-5 males per parent) and only 6% had male production (10-16 males per parent) comparable to that (12-23 males per parent) of seven lineages with a sexual phase (holocyclic) which were examined under the same conditions. The length of prenatal exposure to 10L : 14D increased the production of males. Continuous rearing under 10L : 14D at 12°C adversely affected male production in another intermediate clonal lineage. Temperature was found to affect the production of sexuals and to modify the short day photoperiodic response. The production of males and mating females was higher at 12°C than at 17°C in most of the 20 aforementioned clonal lineages with a partial loss of sexuality. Six lineages were permanently parthenogenetic at 17°C, but two of them produced a few males and the other four a few males and mating females at 12°C. Seven lineages which produced a few males at 17°C, also produced some mating females at 12°C. Lastly, photoperiod similarly affected the production of sexuals in two of the aforementioned clonal lineages, one with a sexual phase and one intermediate, although the regimes for the peak of sexuals were different. In both lineages, however, males appeared in a 0.5-1 h shorter scotophase than mating females.
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