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Population divergence is often quantified using phenotypic variation. However, because sensory abilities are more difficult to discern, we have little information on the plasticity and rate of sensory change between different environments. The Mexican tetra (Astyanax mexicanus) is a fish distributed throughout Southern Texas and Northern Mexico and has evolved troglomorphic phenotypes, such as vestigial eyes and reduced pigmentation, when surface ancestors invaded caves in the past several hundred thousand years. In the early 1900s, surfaceA. mexicanuswere introduced to the karstic Edwards-Trinity Aquifer in Texas. Subsequent cave colonization of subterranean environments resulted in fish with phenotypic and behavioral divergence from their surface counterparts, allowing examination of how new environments lead to sensory changes. We hypothesized that recently introduced cave populations would be more sensitive to light and sound when compared to their surface counterparts. We quantified divergence using auditory evoked potentials (AEPs) and particle acceleration levels (PALs) to measure differences in sound sensitivity, and electroretinography (ERGs) to measure light sensitivity. We also compared these results to measurements taken from native populations and lab-born individuals of the introduced populations. Honey Creek Cave fish were significantly more sensitive than proximate Honey Creek surface fish to sound pressure levels between 0.6 and 0.8 kHz and particle acceleration levels between 0.4 and 0.8 kHz. Pairwise differences were found between San Antonio Zoo surface and the facultative subterranean San Pedro Springs and Blue Hole populations, which exhibited more sensitivity to particle acceleration levels between 0.5 and 0.7 kHz. Electroretinography results indicate no significant differences between populations, although Honey Creek Cave fish may be trending toward reduced visual sensitivity. Auditory thresholds between wild-caught and lab-raised populations of recently invaded fish show significant differences in sensitivity, suggesting that these traits are plastic. Collectively, while these results may point to the rapid divergence ofA. mexicanusin cave habitats, it also highlights the responsive plasticity ofA. mexicanusauditory system to disparate environments. 

Synopsis Communication is a social process and usually occurs in a network of signalers and receivers. While social network analysis has received enormous recent attention from animal behaviorists, there have been relatively few attempts to apply these techniques to communication networks. Communication networks have the potential to offer novel insights into social network studies, and yet are especially challenging subjects, largely because of their unique spatiotemporal characteristics. Namely, signals propagate through the environment, often dissociating from the body of the signaler, to influence receiver behavior. The speed of signal propagation and the signal’s active space will affect the congruence of communication networks and other types of social network; in extreme cases, the signal may persist and only first be detected long after the signaler has left the area. Other signals move more rapidly and over greater distances than the signaler could possibly move to reach receivers. We discuss the spatial and temporal consequences of signaling in networks and highlight the distinction between the physical location of the signaler and the spread of influence of its signals, the effects of signal modality and receiver sensitivity on communication network properties, the potential for feedbacks between network layers, and approaches to analyzing spatial and temporal change in communication networks in conjunction with other network layers.