Literature DB >> 18302998

Developmental plasticity of mating calls enables acoustic communication in diverse environments.

Oliver M Beckers1, Johannes Schul.   

Abstract

Male calls of the katydid Neoconocephalus triops exhibit substantial developmental plasticity in two parameters: (i) calls of winter males are continuous and lack the verse structure of summer calls and (ii) at equal temperatures, summer males produce calls with a substantially higher pulse rate than winter males. We raised female N. triops under conditions that reliably induced either summer or winter phenotype and tested their preferences for the call parameters that differ between summer and winter males. Neither generation was selective for the presence of verses, but females had strong preferences for pulse rates: only a narrow range of pulse rates was attractive. The attractive ranges did not differ between summer and winter females. Both male pulse rate and female preference for pulse rate changed with ambient temperature, but female preference changed more than the male calls. As a result, the summer call was attractive only at 25 degrees C, whereas the slower winter call was attractive only at 20 degrees C. Thus, developmental plasticity of male calls compensates for differences in temperature dependency between calls and preferences and enables the communication system to function in heterogeneous environments. The potential role of call plasticity during the invasion of new habitats is discussed.

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Year:  2008        PMID: 18302998      PMCID: PMC2602675          DOI: 10.1098/rspb.2007.1765

Source DB:  PubMed          Journal:  Proc Biol Sci        ISSN: 0962-8452            Impact factor:   5.349


  8 in total

1.  Induced defenses in response to an invading crab predator: an explanation of historical and geographic phenotypic change.

Authors:  G C Trussell; L D Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2000-02-29       Impact factor: 11.205

Review 2.  Phenotypic plasticity in the interactions and evolution of species.

Authors:  A A Agrawal
Journal:  Science       Date:  2001-10-12       Impact factor: 47.728

3.  What determines the tuning of hearing organs and the frequency of calls? A comparative study in the katydid genus Neoconocephalus (Orthoptera, Tettigoniidae).

Authors:  Johannes Schul; Adam C Patterson
Journal:  J Exp Biol       Date:  2003-01       Impact factor: 3.312

4.  Evolutionary implications of phenotypic plasticity in the hindlimb of the lizard Anolis sagrei.

Authors:  J B Losos; D A Creer; D Glossip; R Goellner; A Hampton; G Roberts; N Haskell; P Taylor; J Ettling
Journal:  Evolution       Date:  2000-02       Impact factor: 3.694

5.  Effects of developmental environment on signal-preference coupling in a Hawaiian cricket.

Authors:  Jaime L Grace; Kerry L Shaw
Journal:  Evolution       Date:  2004-07       Impact factor: 3.694

6.  Adaptive phenotypic plasticity and the successful colonization of a novel environment.

Authors:  Pamela J Yeh; Trevor D Price
Journal:  Am Nat       Date:  2004-09-10       Impact factor: 3.926

7.  Temperature Coupling in the Vocal Communication System of the Gray Tree Frog, Hyla versicolor.

Authors:  H C Gerhardt
Journal:  Science       Date:  1978-03-03       Impact factor: 47.728

8.  Recognition of calls with exceptionally fast pulse rates: female phonotaxis in the genus Neoconocephalus (Orthoptera: Tettigoniidae).

Authors:  Joshua A Deily; Johannes Schul
Journal:  J Exp Biol       Date:  2004-09       Impact factor: 3.312

  8 in total
  13 in total

1.  Sensory-encoding differences contribute to species-specific call recognition mechanisms.

Authors:  J D Triblehorn; J Schul
Journal:  J Neurophysiol       Date:  2009-07-01       Impact factor: 2.714

2.  Dynamic dendritic compartmentalization underlies stimulus-specific adaptation in an insect neuron.

Authors:  Janez Prešern; Jeffrey D Triblehorn; Johannes Schul
Journal:  J Neurophysiol       Date:  2015-04-15       Impact factor: 2.714

Review 3.  Choosiness, a neglected aspect of preference functions: a review of methods, challenges and statistical approaches.

Authors:  Klaus Reinhold; Holger Schielzeth
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2014-11-15       Impact factor: 1.836

4.  Calling song signals and temporal preference functions in the cricket Teleogryllus leo.

Authors:  M M Rothbart; R M Hennig
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2012-09-04       Impact factor: 1.836

5.  Past or present? Relative contributions of developmental and adult conditions to adult immune function and coloration in mallard ducks (Anas platyrhynchos).

Authors:  Michael W Butler; Kevin J McGraw
Journal:  J Comp Physiol B       Date:  2010-12-08       Impact factor: 2.200

6.  Selective phonotaxis in Neoconocephalus nebrascensis (Orthoptera: Tettigoniidae): call recognition at two temporal scales.

Authors:  Joshua A Deily; Johannes Schul
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2008-11-04       Impact factor: 1.836

7.  Dendritic mechanisms contribute to stimulus-specific adaptation in an insect neuron.

Authors:  Jeffrey D Triblehorn; Johannes Schul
Journal:  J Neurophysiol       Date:  2013-08-14       Impact factor: 2.714

8.  Evolution of novel signal traits in the absence of female preferences in Neoconocephalus katydids (Orthoptera, Tettigoniidae).

Authors:  Sarah L Bush; Johannes Schul
Journal:  PLoS One       Date:  2010-08-27       Impact factor: 3.240

9.  Molecular phylogenetics of the genus Neoconocephalus (orthoptera, tettigoniidae) and the evolution of temperate life histories.

Authors:  Robert L Snyder; Katy H Frederick-Hudson; Johannes Schul
Journal:  PLoS One       Date:  2009-09-25       Impact factor: 3.240

10.  Anthropogenic noise causes body malformations and delays development in marine larvae.

Authors:  Natacha Aguilar de Soto; Natali Delorme; John Atkins; Sunkita Howard; James Williams; Mark Johnson
Journal:  Sci Rep       Date:  2013-10-03       Impact factor: 4.379

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