May 26, 2017 by Christopher
Packham report
(Phys.org)—Eusocial insects are
predominantly dependent on chemosensory communication to coordinate social
organization and define group membership. As the social complexity of a species
increases, individual members require a greater diversity of signals. The
communications of highly social insects such as wasps are well documented, but
relatively little is known about the evolutionary transition between solitary
and social living.
An international collaborative of
researchers recently conducted a study of halictid bees in order to determine
how the metabolic cost of chemosensory organs changes during such transitions.
They theorized that changes in social structure would be reflected in changes
to the expensive antennae sensory systems of insects.
The researchers imaged the
antennae of adult females from 36 species that ranged across a
spectrum from completely solitary to highly social, and analyzed sensilla density using digital statistical
software. The tests confirmed their theory: As sociality is gained and lost in
halictid bees, convergent changes occur in both sensilla structures and the
chemical signals of the groups. Social insects invest more in these systems
than solitary bees, and as group complexity increases, communications develop
higher diversity. "Taken together," the authors write, "these
results suggest that there is a strong link between the evolution of social
behavior and investment in communication."
The researchers note that
sensilla density did not increase as sociality was gained; ancestrally solitary
halictids had sensilla densities similar to eusocial species. The researchers
compare this seeming paradox to the evolution of cave-dwelling animal species
that lose the sense of vision, but whose visual organs and brain structures,
while functionally redundant, never become completely vestigial.
However, secondarily solitary
halictids—those bees that switched rapidly from social to solitary—exhibited
marked decreases in sensilla density as communications declined.
"Importantly, the reduction we observed in this group is not a complete
vestigilization. Instead, it represents a decreased investment in antennal
sensilla, perhaps in the absence of complex communication associated with group
living," the authors write.
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