Literature DB >> 28573349

Motion-based signaling in sympatric species of Australian agamid lizards.

Jose A Ramos1, Richard A Peters2.   

Abstract

Signaling species occurring in sympatry are often exposed to similar environmental constraints, so similar adaptations to enhance signal efficacy are expected. However, potentially opposing selective pressures might be present to ensure species recognition. Here, we analyzed the movement-based signals of two pairs of sympatric lizard species to consider how reliable communication is maintained while avoiding misidentification. Our novel approach allows us to quantify signal contrast with plant motion noise at any site we measure, including those utilized by other species. Ctenophorus caudicinctus and Gowidon longirostris differed in display complexity and motor pattern use. They also differed in overall morphology, but their signal contrast scores are strikingly similar. These results demonstrate similar adaptations to their shared environment while maintaining species recognition cues. In contrast, Ctenophorus fordi and Ctenophorus pictus are much closer in appearance, but C. pictus produces considerably higher signal contrast scores, which we suggest is attributable to the absence of territoriality in C. fordi. Taken together, our data provide evidence for adaptation to the local environment in movement-based signals, while also meeting species recognition requirements, but the selective pressure to deal with local conditions is mediated by signal function.

Entities:  

Keywords:  Agamidae; Environmental noise; Signaling; Species recognition; Sympatry

Mesh:

Year:  2017        PMID: 28573349     DOI: 10.1007/s00359-017-1185-5

Source DB:  PubMed          Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol        ISSN: 0340-7594            Impact factor:   1.836


  17 in total

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Authors:  Devi M Stuart-Fox; Adnan Moussalli; Gregory R Johnston; Ian P F Owens
Journal:  Evolution       Date:  2004-07       Impact factor: 3.694

2.  Convergence and the multidimensional niche.

Authors:  Luke J Harmon; Jason J Kolbe; James M Cheverud; Jonathan B Losos
Journal:  Evolution       Date:  2005-02       Impact factor: 3.694

3.  Signaling against the wind: modifying motion-signal structure in response to increased noise.

Authors:  Richard A Peters; Jan M Hemmi; Jochen Zeil
Journal:  Curr Biol       Date:  2007-07-05       Impact factor: 10.834

4.  A comparative study of the evolution of sceloporus push-up displays.

Authors:  E P Martins
Journal:  Am Nat       Date:  1993-12       Impact factor: 3.926

5.  Motion detection in the presence and absence of background motion in an Anolis lizard.

Authors:  L J Fleishman
Journal:  J Comp Physiol A       Date:  1986-11       Impact factor: 1.836

6.  Local adaptation and divergence in colour signal conspicuousness between monomorphic and polymorphic lineages in a lizard.

Authors:  C A McLean; A Moussalli; D Stuart-Fox
Journal:  J Evol Biol       Date:  2014-10-20       Impact factor: 2.411

7.  Habitat-dependent song divergence in the little greenbul: an analysis of environmental selection pressures on acoustic signals.

Authors:  Hans Slabbekoorn; Thomas B Smith
Journal:  Evolution       Date:  2002-09       Impact factor: 3.694

8.  What determines dewlap diversity in Anolis lizards? An among-island comparison.

Authors:  B Vanhooydonck; A Herrel; J J Meyers; D J Irschick
Journal:  J Evol Biol       Date:  2009-02       Impact factor: 2.411

9.  Evolution of Anolis lizard dewlap diversity.

Authors:  Kirsten E Nicholson; Luke J Harmon; Jonathan B Losos
Journal:  PLoS One       Date:  2007-03-07       Impact factor: 3.240

10.  Social context affects tail displays by Phrynocephalus vlangalii lizards from China.

Authors:  Richard A Peters; Jose A Ramos; Juan Hernandez; Yayong Wu; Yin Qi
Journal:  Sci Rep       Date:  2016-08-16       Impact factor: 4.379

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