No abstract

A molecular phylogenetic analysis was conducted in order to reconstruct the evolution of female flightlessness in the geometrid tribe Operophterini (Lepidoptera, Geometridae, Larentiinae). DNA variation in four nuclear gene regions, segments D1 and D2 of 28S rRNA, elongation factor 1a, and wingless, was examined from 22 species representing seven tribes of Larentiinae and six outgroup species. Direct optimization was used to infer a phylogenetic hypothesis from the combined sequence data set. The results obtained confirmed that Operophterini (including Malacodea) is a monophyletic group, and Perizomini is its sister group. Within Operophterini, the genus Malacodea is the sister group to the genera Operophtera and Epirrita, which form a monophyletic group. This relationship is also supported by morphological data. The results suggest that female flightlessness has evolved independently twice: first in the lineage of Malacodea and, for the second time, in the lineage of Operophtera after its separation from the lineage of Epirrita. An alternative reconstruction (i.e. recovery of flight ability in an ancestor of Epirrita) appears unlikely for various reasons. The similarities shared by Epirrita with a basal representative of Perizomini, Perizoma didymatum, allow the proposal of a sequence of evolutionary events that has led to flightlessness. It is likely that the transition to female flightlessness in the two lineages of Operophterini occurred after the colonization of stable forest habitats, followed by the evolution of a specific set of permissive traits, including larval polyphagy, limited importance of adult feeding, and adult flight during the cold months of the season.

Abstract. The geometrid genusCleorodes is shown to belong in the tribe Gnophini (sensu lato) and not in Boarmiini as previously assumed. The conclusion is based on an analysis of morphological characters of a number of genera in these tribes. Moreover, the result is unambiguously supported by a phylogenetic analysis of DNA sequence variation in three nuclear gene regions (segments D1 and D2 of 28S rRNA, and elongation factor 1 ) and a mitochondrial gene, cytochrome oxidase-1. The phylogenetic hypothesis is based on a combined sequence data set, which was analysed using direct optimisation.

Abstract. Analysis of the mitochondrial DNA (mtDNA) control region (CR) was used to examine the dispersal of females of a geometrid moth, Epirrita autumnata, in Fennoscandia. A 542-bp-portion of the CR of 200 individuals from four northern and four southern localities was sequenced. The mtDNA CR of E. autumnata contains a substantial amount of variation as a total of 108 mtDNA haplotypes were observed. Between the northern and the southern localities (~1100 km), there was a moderate level of genetic differentiation (FST = 0.128). The amount of variation in the mtDNA CR of E. autumnata was lower in the north than in the south. The reduction in genetic variability may result from a combination of historical bottlenecks that date back to the post-glacial recolonization of Fennoscandia and, present-day bottlenecks due to the northern E. autumnata populations experiencing repeated outbreaks followed by collapse in population size. On a small spatial scale (0.6-19 km), within the northern and southern areas, no genetic differentiation was detected suggesting ongoing gene flow due to the dispersal of E. autumnata females among the localities. This finding was contrary to our earlier expectation of poor flying ability of E. autumnata females.

The organization of the mitochondrial DNA (mtDNA) control region (CR) of the autumnal moth, Epirrita autumnata, is described. The E. autumnata CR presents a distinct type of lepidopteran CR with domains of non-repetitive and repetitive sequences. The CRs show considerable length variation owing to a variable number of short approximately 29-bp sequence blocks that are repeated between 6 and 14 times in tandem. The organization of such a tandem array is unique among the insect CRs examined so far. Furthermore, the E. autumnata CR, which may reach 1075 bp in length, is considerably longer than previously reported lepidopteran CRs, which reach 311-499 bp in length. Like other lepidopteran CRs, the E. autumnata CR contains two long homopolymer runs that may be involved in mtDNA replication and (or) transcription.