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Locustatachykinin-immunoreactive (LomTK-IR) interneurons were found to be associated with the central complex, a prominent neuropil region of the insect brain. The structures and development of this set of brain interneurons was studied from the embryo onward in the beetle Tenebrio molitor, showing individual neurons that persist from the late embryo to the adult stage. Their essential structural characteristics were already present in the late embryo, but distinct parts of their arborization patterns became newly formed throughout development. Using a combination of immunohistochemistry and single-cell injection, we demonstrated minute structural changes, allowing a characterization of structural plasticity of identifiable, persistent, neuropeptidergic neurons throughout ontogenesis. Furthermore, this study has provided new information about basic principles of central brain neuroanatomy and the development of a distinct midbrain region of the insect brain, the central complex. The development of its basic connections, the connections between the fan-shaped body and the protocerebral bridge, and the compartmentation of these neuropil regions were shown, using LomTK-IR neurons as marker structures. These basic features of the central complex-associated LomTK-immunopositive neurons were formed in the embryonic brain, whereas in metamorphosis, reorganization of these persistent interneurons was restricted to the formation of a precisely defined projection of their side branches.

The set of neurones innervating the dorsal longitudinal muscles was studied with cobalt and nickel backfills in: (1) larval and adult locusts (Schistocerca gregaria and Locusta migratoria), (2) the larval and adult beetle (Zophobas morio), and (3) various segments of these insect species. In all specimens 11 neurones were encountered, which can be subdivided into a group of 7 motoneurones that stem from the next anterior ganglion and 4 neurones located in the ganglion of the segment containing the muscles. The latter group comprises 2 contralateral and 2 medial somata, of which one is a dorsal unpaired median neurone. The results were analysed under different aspects. This neural set and the basic structure of the dendritic fields is similar in: (1) different segments (serial homology), (2) the larval stage and imago of the same species with or without a pronounced metamorphosis (ontogeny), and (3) the studied hemi- and holometabolous insects (phylogeny). Our results support the notion that the structure of these neurones is conserved irrespectively of changes in the periphery and strategy of postembryonic development.