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In the present study, we present the full sequence of the mitochondrial genome of the African desert locust Schistocerca gregaria gregaria. The size of 15625 bp reported matches very well with mitochondrial genomes of other Orthopteriodea. The mitochondrial genome comprises 13 protein-coding genes, two ribosomal RNAs and 22 t-RNAs with two t-RNA (trnD and trnK) rearrangements that are typical for the taxon Caelifera. We compared the sequence with 12 mitochondrial genes of Schistocerca gregaria flaviventris and Schistocerca americana and used some of these data to construct phylogenetic trees, which confirm the close relationship between the two subspecies S. g. flaviventris and S. g. gregaria. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 99, 296–305. ADDITIONAL KEYWORDS: gene organization – phylogeny – Schistocerca americana – subspecies.

Because of the scarcity of polymorphic genetic markers, only a few genetic studies on the population structure of the desert locust, Schistocerca gregaria, have been carried out. We isolated and characterized nine polymorphic dinucleotide microsatellite loci. These markers were evaluated using individuals from Niger and Senegal. Seven of these microsatellite markers are also applicable to the nongregarious subspecies Schistocerca gregaria flaviventris. Cross-species applicability was limited to one of the loci in the sister species S. americana and in the locust Locusta migratoria.

Juvenile hormone synthesis in adult worker honey bees was measured by an in vitro corpora allata bioassay. Adult queenless workers exhibit higher rates of juvenile hormone biosynthesis than queenright workers. Hormone synthesis is not correlated with the volume of the glands. Extract of queen mandibular glands, applied to a dummy, reduces juvenile hormone biosynthesis in caged queenless workers to the level of queenright workers. The same result was obtained with synthetic (E)-9-oxo-2-decenoic acid, the principal component of the queen mandibular gland secretion. This pheromonal primer effect may function as a key regulating element in maintaining eusocial colony homeostasis. The presence of brood does not affect the hormone production of the corpora allata.

A culture system for honeybeen fat body and ovary was developed that supported optimal levels of protein synthesis by the explanted tissues. Abdominal body wall preparations of honeybee workers and queens, with adhering fat body, and ovaries of egg-laying queens were incubated in a culture medium designed to match honeybee hemolymph composition as closely as possible. Incorporation of [3H]eucine into soluble tissue proteins was measured. The new medium makes possible rates of tracer incorporation into fat body proteins that are up to three times higher than other media tested. When the tracheal system of the organs was let intact and open to the air during incubation, protein synthesis increased 17-fold (fat body) or 15-fold (ovary) as compared to preparations without open tracheas. After explantation into the medium, labeled proteins were synthesized at a highly variable rate for 10 h, probably due to wound response, and at a constant rate for the next 60 h. In contrast, ovarian protein synthesis occurred at a constant rate for at least 20 h and showed no wound response. The rate of tracer incorporation into fat body proteins was 3.2 times greater in tissues from the queen. This culture system is therefore suitable for a variety of investigations in honeybeen development and reproduction.