Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 May 8:6:e4722.
doi: 10.7717/peerj.4722. eCollection 2018.

The brown anole dewlap revisited: do predation pressure, sexual selection, and species recognition shape among-population signal diversity?

Affiliations

The brown anole dewlap revisited: do predation pressure, sexual selection, and species recognition shape among-population signal diversity?

Simon Baeckens et al. PeerJ. .

Abstract

Animal signalling structures are amongst the most variable characteristics, as they are subjected to a diversity of selection pressures. A well-known example of a diverse signalling system in the animal kingdom is the dewlap of Anolis lizards. Dewlap characteristics can vary remarkably among and within species, and also between sexes. Although a considerable amount of studies have attempted to disentangle the functional significance of the staggering dewlap diversity in Anolis, the underlying evolutionary processes remain elusive. In this study, we focus on the contribution of biotic selective pressures in shaping geographic variation in dewlap design (size, colour, and pattern) and dewlap display behaviour at the intraspecific level. Notably, we have tried to replicate and extend previously reported results hereof in both sexes of the brown anole lizard (Anolis sagrei). To do this, we assembled a dataset consisting of 17 A. sagrei heterogeneous island populations from the Caribbean and specifically tested whether predation pressure, sexual selection, or species recognition could explain interpopulational variation in an array of dewlap characteristics. Our findings show that in neither males nor females estimates of predation pressure (island size, tail break frequency, model attack rate, presence of predatory Leiocephalus lizards) or sexual selection (sexual size dimorphism) could explain variation in dewlap design. We did find that A. sagrei males from larger islands showed higher dewlap display intensities than males from smaller islands, but the direct connection with predation pressure remains ambiguous and demands further investigation. Last, we could show indirect support for species recognition only in males, as they are more likely to have a 'spotted' dewlap pattern when co-occurring with a higher number of syntopic Anolis species. In conclusion, we found overall limited support for the idea that the extensive interpopulational variability in dewlap design and use in A. sagrei is mediated by variation in their biotic environment. We propose a variety of conceptual and methodological explanations for this unexpected finding.

Keywords: Anolis sagrei; Caribbean islands; Clay models; Dewlap diversity; Display behaviour; Lizards; Predation pressure; Visual signalling system.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Figure 1
Figure 1. Sampling locations of the populations of study across the Caribbean.
(1) Soroa (Cuba), population 1; (2) Soroa (Cuba) population 2; (3) Grand Cayman; (4) Santa Clara (Cuba); (5) South Bimini; (6) Chub Cay; (7) Andros; (8) Crooked Island; (9) Acklins; (10) San Salvador; (11) Staniel Cay; (12) Pidgeon Cay; (13) Grand Bahama; (14) South Abaco; (15) Cayman Brac; (16) Little Cayman; (17) Jamaica.
Figure 2
Figure 2. Clay model of a brown anole used for estimating predation pressure.
Photograph of a clay Anolis model used for estimating predation pressure: (A) an intact model; (B) a recollected model with predation marks. Picture by Tess Driessens.

References

    1. Andersson SJ, Örnborg J, Andersson M. Ultraviolet sexual dimorphism and assortative mating in blue tits. Proceedings of the Royal Society B: Biological Sciences. 1998;265(1395):445–450. doi: 10.1098/rspb.1998.0315. - DOI
    1. Baeckens S, Martín J, Garcia-Roa R, Pafilis P, Huyghe K, Van Damme R. Environmental conditions shape the chemical signal design of lizards. Functional Ecology. 2018;32(2):566–580. doi: 10.1111/1365-2435.12984. - DOI
    1. Bateman P, Fleming P. To cut a long tail short: a review of lizard caudal autotomy studies carried out over the last 20 years. Journal of Zoology. 2009;277(1):1–14. doi: 10.1111/j.1469-7998.2008.00484.x. - DOI
    1. Benjamini Y, Hochberg Y. Controlling the false discovery rate: a practical and powerful approach to multiple testing. Journal of the Royal Statistical Society Series B: Statistical Methodology. 1995;57(1):289–300.
    1. Bernal XE, Rand AS, Ryan MJ. Acoustic preferences and localization performance of blood-sucking flies (Corethrella coquillett) to tungara frog calls. Behavioral Ecology. 2006;17(5):709–715. doi: 10.1093/beheco/arl003. - DOI

LinkOut - more resources