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Abstract Morphology has long been used to classify and identify living organisms. However, taxonomic descriptions are often limited to qualitative descriptions of size and shape, making identification difficult due to the subjective language used to describe complex shapes. Additionally, for some taxa, there are few reliable qualitative characters available for delimitation that have yet to be tested objectively in a phylogenetic context. Solifugae is one such example. The order, Solifugae, is recognized from the other arachnid orders by the possession of large, powerful jaws or chelicerae. Male cheliceral morphology is the leading diagnostic character system in solifuge systematics and is the basis for much of solifuge current taxonomy. Female chelicerae, on the other hand, are reportedly deeply conserved and much of the species identification is based on female operculum morphology. To elucidate patterns of chelicerae and opercula trait evolution within the solifuge family, Eremobatidae, we used a 2-dimenstional morphological analysis using an Elliptical Fourier approach for closed outlines, in addition to an analysis of traditionally used measures in a phylogenetic context. Using ancestral state reconstruction and ultra-conserved elements, we assessed the taxonomic utility of female cheliceral and opercular morphology, and we evaluated which male morphological characters reflect shared, derived ancestry. Investigation into ubiquitously used character sets, in addition to newly proposed characters herein, illustrates the complex evolution of traits with high levels of convergence. Our results provide taxonomic insight into future, higher level taxonomic revisions of Eremobatidae. 

Abstract Many herbivorous insect species are capable of hijacking plant development to induce novel plant organs called galls. In most groups of galling insects, the insect organs and molecular signals involved in gall induction are poorly understood. We focused on gall wasps (Hymenoptera:Cynipidae), the second largest clade of gall inducers (~1,400 spp.), for which the developmental stages and organs responsible for gall development are unclear. We investigated the female metasomal anatomy of 69 gall-inducing and 29 non-gall-inducing species across each of the major lineages of Cynipoidea, to test relationships between this lifestyle and the relative size of secretory organs. We confirmed that the venom apparatus in gall-inducing species is greatly expanded, although gall-inducing lineages vary in the relative size of these glands. Among these gallers, we measured the largest venom gland apparatus relative to body size ever recorded in insects. Non-galling inquiline species are accompanied by a reduction of this apparatus. Comparative microscopic analysis of venom glands suggests varying venom gland content across the lineages. Some oak gallers also had enlarged accessory glands, a lipid-rich organ whose function remains unclear, and which has not been previously studied in relation to gall formation. Together, the massive expansion of secretory organs specifically in gall-inducing species suggests a role of these secretions in the process of gall formation, and the variance in size of venom glands, accessory glands, and the contents of these glands among gallers, suggests that gall formation across this clade is likely to employ a diversity of molecular strategies.