Mesozoic rocks with exceptional preservation of marine arthropods are known worldwide but largely restricted to mid-high latitudes. The scarcity of assemblages with exceptional preservation in low, tropical latitudes greatly limits our understanding of the origins of several modern groups and the evolution of tropical biotas through time. Here, we report the oldest crown Cumacea, or 'comma' shrimp (Arthropoda: Eumalacostraca: Peracarida) with modern familial affinities, from a new mid-Cretaceous (95-90 Ma) Lagerstätte in tropical South America. Cumaceans have one of the poorest fossil records among marine arthropods, despite today being abundant and speciose benthic organisms associated with fine-grained sediments with high fossilization potential. Eobodotria muisca gen. et sp. nov., found in mass accumulation surfaces, preserves with detail the gut, mouth parts, thoracic legs/pereopods, pleopods, uropods bearing setae, antennal flagella and even small eyes bearing ommatidia. These features, rarely preserved in fossil crustaceans, plus the large sample size (greater than 200 individuals, 6-8 mm long), allow us to discuss phylogenetic/systematic aspects and explore possible mechanisms behind their unusual accumulation. Eobodotria bridges an approximately 165 Myr gap in the cumacean fossil record, provides a reliable calibration point for phylogenetic studies and expands our understanding of exceptional preservation in past and present tropical settings.
The evolutionary origins of advanced eusociality, one of the most complex forms of phenotypic plasticity in nature, have long been a focus within the field of sociobiology. Although eusocial insects are known to have evolved from solitary ancestors, sociogenomic research among incipiently social taxa has only recently provided empirical evidence supporting theories that modular regulation and deeply conserved genes may play important roles in both the evolutionary emergence and elaboration of insect sociality. There remains, however, a paucity of data to further test the biological reality of these and other evolutionary theories among taxa in the earliest stages of social evolution. Here, we present brain transcriptomic data from the incipiently social small carpenter bee, Ceratina calcarata, which captures patterns of cis-regulation and gene expression associated with female maturation, and underlying two well-defined behavioural states, foraging and guarding, concurrently demonstrated by mothers and daughters during early autumn. We find that an incipiently social nest environment may dramatically affect gene expression. We further reveal foraging and guarding behaviours to be putatively caste-antecedent states in C. calcarata, and offer strong empirical support for the operation of modular regulation, involving deeply conserved and differentially expressed genes in the expression of early social forms.
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