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Abstract Stomatopods are well studied for their unique visual systems, which can consist of up to 16 different photoreceptor types and 33 opsin proteins expressed in the adults of some species. The light‐sensing abilities of larval stomatopods are comparatively less well understood with limited information about the opsin repertoire of these early‐life stages. Early work has suggested that larval stomatopods may not possess the extensive light detection abilities found in their adult counterparts. However, recent studies have shown that these larvae may have more complex photosensory systems than previously thought. To examine this idea at the molecular level, we characterized the expression of putative light‐absorbing opsins across developmental stages, from embryo to adult, in the stomatopod species Pullosquilla thomassini using transcriptomic methods with a special focus on ecological and physiological transition periods. Opsin expression during the transition from the larval to the adult stage was further characterized in the species Gonodactylaceus falcatus. Opsin transcripts from short, middle, and long wavelength‐sensitive clades were found in both species, and analysis of spectral tuning sites suggested differences in absorbance within these clades. This is the first study to document the changes in opsin repertoire across development in stomatopods, providing novel evidence for light detection across the visual spectrum in larvae.

We sequenced the complete mitochondrial genomes of two bat fly species within the Nycteribiidae (Diptera: Hippoboscoidea) – Dipseliopoda setosa (Cyclopodiinae) and Basilia ansifera (Nycteribiinae). Both mitogenomes were complete and contained 13 protein-coding genes, 22 tRNAs, and two rRNAs. Relative to the inferred ancestral gene order of dipteran mitochondrial genomes, no rearrangements were identified in either species. There were large differences in size between the two genomes, with D. setosa having a larger genome (19,164 bp) than B. ansifera (16,964 bp); both species had larger genomes than two previously published Streblidae bat fly species (e.g., Paradyschiria parvula and Paratrichobius longicrus). The increased genome sizes were due to expansions in the control region and the non-coding region downstream of the light-strand origin of replication. Additional differences between the two mitogenomes included a significantly longer cox3 gene in B. ansifera and a longer nad1 gene in D. setosa. Interestingly, both genomes also had the lowest GC content (D. setosa – 15.9%; B. ansifera – 17.0%) of any available Hippoboscoidea mitochondrial genome (18.8–23.9%). These mitogenomes represent the first sequences from species within the bat fly family Nycteribiidae. The sequence data here will provide a foundation for continued studies of genome evolution more generally within obligate blood-feeding ectoparasites, and specifically for the bat flies as vectors of significant ‘bat-associated’ viruses and microorganisms.

We sequenced the complete mitochondrial genomes of one Iolania perkinsi (Kirkaldy 1902) and one Oliarus cf. filicicola (Kirkaldy 1909) planthopper (Hemiptera: Fulgoroidea: Cixiidae) from Volcano Village, located on the eastern flank of Mauna Loa. The I. perkinsi complete mitogenome is 14,949 bp in length and contains 13 protein-coding genes, 22 tRNAs and 2 rRNAs. The O. cf. filicicola nearly complete mitogenome is 15,196 bp in length due to an expanded (but incomplete) control region, and contains all of the typical metazoan genes: 13 protein-coding genes, 22 tRNAs and two rRNAs. Relative to the inferred ancestral gene order of insect mitochondrial genomes, no rearrangements were identified in either species. In addition to the shorter control region in I. perkinsi, the differences between the two mitogenomes consist of longer cox1, cox2, cob, nad1, nad5, nad6 genes but shorter nad4 gene in I. perkinsi relative to O. cf. filicicola. These mitogenomes represent the first sequences from species within the Hawaiian Cixiidae. The sequence data here will provide a foundation for continued studies of speciation patterns and dynamics of evolutionary radiation across Hawaiian planthoppers.

A widely accepted model for the evolution of cave animals posits colonization by surface ancestors followed by the acquisition of adaptations over many generations. However, the speed of cave adaptation in some species suggests mechanisms operating over shorter timescales. To address these mechanisms, we used Astyanax mexicanus, a teleost with ancestral surface morphs (surface fish, SF) and derived cave morphs (cavefish, CF). We exposed SF to completely dark conditions and identified numerous altered traits at both the gene expression and phenotypic levels. Remarkably, most of these alterations mimicked CF phenotypes. Our results indicate that many cave-related traits can appear within a single generation by phenotypic plasticity. In the next generation, plasticity can be further refined. The initial plastic responses are random in adaptive outcome but may determine the subsequent course of evolution. Our study suggests that phenotypic plasticity contributes to the rapid evolution of cave-related traits in A. mexicanus.