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The scent of a predator: the effects of chemical threats on shell selection in the hermit crabs, Pagurus samuelis and Pagurus hirsutiusculus 1Department Joanelle Hernández1 & Eric Sanford2 of Biology, Brown University; 2Section of Evolution and Ecology, University of California, Davis • Predators can affect prey by: 1) reducing the prey population through consumption and 2) inducing phenotypic changes in their prey. • Changes arising in prey populations from chemical predator threats can be morphological, physiological, behavioral or life-historical. • Indirect or chemically signaled trait-mediated impacts have been studied less. However, their implications are all-encompassing within ecological communities because their effects are transferred across other species which come into contact with the prey. • Hermit crabs, because they exhibit complex behaviors and respond to chemical cues, are an ideal model to study trait-mediated behavioral plasticity. Shell selection in hermit crabs is a compromise between shell traits and different aspects of fitness. For example, hermit crab growth, survival, and brood size depend on the characteristics of chosen shell species. In Horseshoe Cove, two Pagurid species occupy up to 12 different species of gastropod shells. 1) Do hermit crabs respond to predation threat by selecting shells that are better at protecting them from their predators? 2) Do hermit crabs differentiate between, and respond to, chemical signals across multiple phyla of predators? 3) Do Pagurus hirsutiusculus and Pagurus samuelis respond differently to these cues? Pycnopodia helianthoides Cancer antennarius • Field surveys of tidepools in Horseshoe Cove quantified patterns of shell use. In each laboratory trial, individual hermit crabs were given a choice of two species of gastropod shells matched as closely as possible in internal volume. Hermit crabs were exposed to predator effluent (n=6), either C. antennarius (Cancer crab) or P. helianthoides (sea star), or a no-effluent control (n=6). Naked hermit crabs were placed in a culture dish halfway between the two shells, observations were taken for the first five minutes, and time to first shell choice was noted (latency). Shell selection was recorded at fifteen minutes, two and six hours. • For each species, crabs were grouped into small (shell length less than 12mm) and large (shell length greater than 12mm) categories. Small Littorine Nucella Tegula Other Predation Pagurus hirsutiusculus Pagurus samuelis 150 120 Effluent Control A 90 AB 60 30 B B n=12 Latency (seconds) Latency (seconds) 150 Effluent Control 120 N.S. 90 ? ? Pagurus samuelis Cancer 30 P.hirsutiusculus n=12 Cancer Pycnopodia 1) Only Pagurus samuelis showed sensitivity to Cancer effluent. Still, they did not select the thicker Nucella lamellosa shell that may offer more crab protection. Pycnopodia Predator Treatment Predator Treatment • Pagurus samuelis responded to Cancer effluent and took longer to make the first shell choice. Individuals exposed to the sea star Pycnopodia selected shells faster, although this trend was not significant. Shell Choice Shell combinations P. samuelis P. hirsutiusculus Cancer Pycnopodia (Effluent and (Effluent and control) control) TF vs NO NO vs TF TF vs NL NO vs NL TF vs NO NO vs TF TF vs NL NO vs NL Studies suggest that Pycnopodia is able to give off an active or inactive chemical cue. Further experiments are needed to test how these states affect hermit crabs’ ability to sense these predators. Legend TF= Tegula funebralis NO= Nucella ostrina Activity level or frequency of shell switching may better indicate sensitivity to predator cues. Alternatively, hermit crab species may differ in their ability to detect predators. 2) Although there was a trend in Pagurus spp. response to Pycnopodia cues, it was not statistically significant. This suggests that hermit crabs may be unable to detect some predators. • Pagurus hirsutiusculus’ time to first shell choice did not differ between individuals exposed to predator effluent and control water in either predator treatment. = shell selected Pagurus hirsutiusculus Large 60 0 0 • Large P.samuelis is most commonly in Tegula, whereas P.hirsutiusculus often use Nucella Pagurus samuelis Large Small Tegula funebralis Nucella ostrina Nucella lamellosa NL= Nucella lamellosa Acknowledgments: This research was supported by grant #DBI-0453251 to S.L. Williams from the National Science Foundation. Thank you to the BML community and all people who contributed to this project. • Choice made after 15 min seldom changed after 2 hrs or 6 hrs. • P. samuelis chose Tegula funebralis, regardless of other shell options or presence of predator cues. References: Bertness, M. D. 1981. The American Naturalist 118, 432. Preisser, E. L., et al. 2005. Ecology 86, 501. • P. hirsutiusculus chose Nucella ostrina shells. McClintock. 1985. J. Exp. Mar. Biol. Ecol. 88, 271. Rotjan, R. et al. 2004. Behav. Ecol. Sociobiol 56, 171. 3) Shell preference was species-specific: 100% of Pagurus samuelis chose Tegula funebralis while 100% of P. hirsutiusculus picked Nucella ostrina. Shell selection in the laboratory matched patterns seen in the field. Shell choice may reflect trade-offs among crushing resistance, shell weight influence on escape speed, and room for embryo brooding. Considering these factors together could explain crabs’ failure to pick a thicker shell. Although hermit crabs appear to respond to predator cues in some cases (by changing speed of shell selection), they appear remarkably consistent in their shell preferences. These choices may reflect the optimal balance of multiple costs and benefits conferred by different shell types.