Phylogenetic position of the mite family Myobiidae within the infraorder Eleutherengona (Acariformes) and origins of parasitism in eleutherengone mites

The position of the family Myobiidae in the infraorder Eleutherengona (Prostigmata) was analyzed with a cladistic parsimony approach for the first time. Species of the genera Anystis von Heyden (Anystidae), Pomerantzia Baker (Pomerantziidae), and Walytydeus Kuznetzov (Paratydeidae) were selected as outgroups. Among Eleutherengona, species of the following genera were selected as ingroup taxa: Hirstiella Berlese (Pterygosomatidae), Eucheyletia Baker, Cheyletiella Canestrini (Cheyletidae), Syringophilus Heller (Syringophilidae), Tarsocheylus Berlese (Tarsocheylidae), Heterocheylus Lombardini (Heterocheylidae), Pygmephorus Kramer (Pygmephoridae), Raphignathus Dugès (Raphignathidae), Neognathus Willmann (Caligonellidae), Storchia Oudemans (Stigmaeidae), and Tuckerella Womersley (Tuckerellidae). Three most parsimonious trees with similar topology were obtained. In all these trees, the family Myobiidae is situated outside of the clade joining the higher Raphignathae (Raphignathoidea and Cheyletoidea) and represents a branch within the earlier derivative Raphignathae. This result is based primarily on characters from leg setation and postembryonic development. The conclusion from this topology is that myobiid mites have developed some gnathosomal structures convergently with Cheyletoidea, including the stylet-like chelicerae and stylophore fused with the subcapitulum. The evolution of animal eleutherengone parasitism is discussed. Parasitism arisen independently in numerous phyletic lineages or superfamilies of Eleutherengona. The representatives of some phylogenetically distant eleutherengone lineages developed similar adaptations to predation and parasitism. However, in spite of some similarities in these adaptations, the evolutionary trends and pathways for switching to a parasitic mode of life are quite different in particular eleutherengone lineages.