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Signals and receiver responses often vary across a species’ geographic range. Effective communication requires a match between signal and receiver response, so there is much interest in the developmental mechanisms that maintain this link. Two potential mechanisms are genetic covariance between signal and receiver response and plasticity where individuals adjust their phenotype based on their partner’s phenotype. Here, we test how plasticity contributes to geographic variation in individual face recognition in Polistes fuscatus wasps. Previous work has shown that P. fuscatus from Michigan, USA (MI) have variable facial patterns used for individual recognition, while P. fuscatus from central Pennsylvania, USA (PA) lack variable facial patterns and are unable to learn individual conspecifics. We experimentally altered rearing environment, so wasps were either reared with their own population or in a common garden with wasps from both populations. Then, we tested the wasps’ capacity to learn and remember individual conspecific faces. Consistent with previous work, MI wasps reared with MI wasps were adept at learning conspecific faces, while PA wasps reared with PA wasps were unable to learn conspecific faces. However, MI and PA wasps reared in a common garden developed similar, intermediate capacity for individual face learning. These results indicate that individual face learning in Polistes wasps is highly plastic and responsive to the social environment. Plasticity in receiver responses may be a common mechanism mediating geographic differences in non-sexual signaling systems and may play a role in maintaining links between signals and receiver responses in geographically variable communication systems.

 

Each fall, millions of monarch butterflies across the U.S. and Canada migrate up to 4,000 km to overwinter in the same cluster of mountaintops in central Mexico. In spring, these migrants mate and remigrate northwards to repopulate their northern breeding territory over 2-4 partially overlapping generations. Because each migrant monarch completes only part of this round trip and does not return to the overwintering site, this navigational task cannot be learned from the prior generation. The number of monarchs completing the journey has dramatically declined in the past decades, coincident with the decreased availability of their milkweed host plant. The U.S., Mexico, and Canada have invested tremendous resources into monarch conservation efforts, including enacting specific policy initiatives, public outreach programs, and habitat protection and restoration projects. The US invested over $11 million between 2015-2017 alone [1]. Developing a tracking technology for monarch can be a key in these efforts, providing, for instance, detailed understanding of habitat use during migratory flight and dependence on weather conditions. Furthermore, it can significantly benefit animal research, and agricultural and environmental science. 

The monarch butterfly (Danaus plexippus) complements its iconic migration with diapause, a hormonally controlled developmental programme that contributes to winter survival at overwintering sites. Although timing is a critical adaptive feature of diapause, how environmental cues are integrated with genetically‐determined physiological mechanisms to time diapause development, particularly termination, is not well understood. In a design that subjected western North American monarchs to different environmental chamber conditions over time, we modularized constituent components of an environmentally‐controlled, internal diapause termination timer. Using comparative transcriptomics, we identified molecular controllers of these specific diapause termination components. Calcium signalling mediated environmental sensitivity of the diapause timer, and we speculate that it is a key integrator of environmental condition (cold temperature) with downstream hormonal control of diapause. Juvenile hormone (JH) signalling changed spontaneously in diapause‐inducing conditions, capacitating response to future environmental condition. Although JH is a major target of the internal timer, it is not itself the timer. Epigenetic mechanisms are implicated to be the proximate timing mechanism. Ecdysteroid, JH, and insulin/insulin‐like peptide signalling are major targets of the diapause programme used to control response to permissive environmental conditions. Understanding the environmental and physiological mechanisms of diapause termination sheds light on fundamental properties of biological timing, and also helps inform expectations for how monarch populations may respond to future climate change.