Adult body size is the result of important environmental, maternal and/or genetic effects acting on animals during development. Here we investigate how sexual size dimorphism (SSD) develops in seven species of Odonata: Anax imperator, Cordulegaster boltonii, Onychogomphus uncatus, Oxygastra curtisii (Anisoptera), Cercion lindeni, Ischnura graellsii and Platycnemis acutipennis (Zygoptera). SSD of both the last larval and adult stages of the same individuals, which were reared under laboratory conditions, was measured. The aims were to investigate (i) whether SSD develops during the larval stage, (ii) the direction of larval and adult SSD, and (iii) whether the direction of adult SSD can be predicted by the mating system of a given species (e.g. males of territorial species being larger than females and the opposite for non-territorial species). We found that although larval differences in size may be present between the sexes, these are not necessarily shown in the adult stage (they may change or disappear). Also, the mating system was not related to patterns of adult SSD. Differences in SSD in larvae may be caused by differential use of resources via differential niche-utilisation or sex-specific growth patterns. We highlight the fact that sexual selection favouring large male size and fecundity selection, which selects for large females may be acting on the observed patterns in SSD in adults.
Co-occurrence of species with similar trophic requirements, such as odonates, seems to depend both on them occupying different microhabitats and differing in their life-cycles. The life cycles of the dragonflies Boyeria irene and Onychogomphus uncatus were studied in two consecutive years, mainly by systematic sampling of larvae in seven permanent head courses that constitute the upper basin of the River Águeda, western Spain, in the central part of the ranges of these two species. The size ranges of the last five larval stadia of both species were established based on biometric data. The eggs of the egg-overwintering aeshnid hatched in late spring and early summer and for the gomphid hatching peaked in middle-late summer. Both species showed mixed voltinism with "cohort splitting". B. irene had a dominant three-year development (partivoltinism), with some developing in two years (semivoltinism). O. uncatus requires four, sometimes three years to complete development (all partivoltine). B. irene larvae spent the winter before emergence in the last three, maybe four stadia, as a "summer species". O. uncatus mainly behaved as a "spring species", most larvae spending the last winter in the final larval stadium.