Hexamerins are hemocyanin-related haemolymph proteins that are widespread in insects and may accumulate to extraordinarily high concentrations in larval stages. Hexamerins were originally described as storage proteins that provide amino acids and energy for non-feeding periods. However, in recent years other specific functions like cuticle formation, transport of hormones and other organic compounds, or humoral immune defense have been proposed. During evolution, hexamerins diversified according to the divergence of the insect orders. Within the orders, there is a notable structural diversification of these proteins, which probably reflects specific functions. In this paper, the different possible roles of the hexamerins are reviewed and discussed in the context of hexamerin phylogeny., Thorsten Burmester, and Lit
The monophyly of the Endopterygota is supported primarily by the specialized larva without external wing buds and with degradable eyes, as well as by the quiescence of the last immature (pupal) stage; a specialized morphology of the latter is not an endopterygote groundplan trait. There is weak support for the basal endopterygote splitting event being between a Neuropterida + Coleoptera clade and a Mecopterida + Hymenoptera clade; a fully sclerotized sitophore plate in the adult is a newly recognized possible groundplan autapomorphy of the latter. The molecular evidence for a Strepsiptera + Diptera clade is differently interpreted by advocates of parsimony and maximum likelihood analyses of sequence data, and the morphological evidence for the monophyly of this clade is ambiguous. The basal diversification patterns within the principal endopterygote clades (\"orders\") are succinctly reviewed. The truly species-rich clades are almost consistently quite subordinate. The identification of \"key innovations\" promoting evolutionary success (in terms of large species numbers) is fraught with difficulties., Niels P. Kristensen, and Lit