Quantitative genetics of breeding coloration in sand lizards; genic capture unlikely to maintain additive genetic variance

  • Anderholm S, Olsson M, Wapstra E, Ryberg K (2004) Fit and fat from enlarged badges: a field experiment on male sand lizards. Proc R Soc Lond B 271:S142–S144

    Article 

    Google Scholar
     

  • Aghasyan A, Avci A, Tuniyev B, Lymberakis P, Andrén C, Cogălniceanu D et al. (2021) Lacerta agilis. The IUCN Red List of Threatened Species 2021:e.T157288A49644624. https://doi.org/10.2305/IUCN.UK.2021-2.RLTS.T157288A49644624.en

  • Baur J, Berger D (2020) Experimental evidence for effects of sexual selection on condition-dependent mutation rates. Nat Ecol Evol 4:737–744

    Article 
    PubMed 

    Google Scholar
     

  • Bonduriansky R, Day T (2009) Nongenetic inheritance and its evolutionary implications. Annu Rev Ecol Evol Syst 40:103–125

    Article 

    Google Scholar
     

  • Bourret A, Bélisle M, Pelletier F, Garant D (2017) Evolutionary potential of morphological traits across different life‐history stages. J Evol Biol 30:616–626

    Article 
    CAS 
    PubMed 

    Google Scholar
     

  • Burkhard TT, Matz M, Phelps SM (2020) Genomic heritability of song and condition in wild singing mice. Preprint at bioRxiv:2020.2010.2008.321141

  • Cally JG, Stuart-Fox D, Holman L (2019) Meta-analytic evidence that sexual selection improves population fitness. Nat Comm 10:2017

    Article 

    Google Scholar
     

  • Connallon T (2010) Genic capture, sex linkage, and the heritability of fitness. Am Nat 175:564–576

    Article 
    PubMed 

    Google Scholar
     

  • Dugand RJ, Tomkins JL, Kennington WJ (2019) Molecular evidence supports a genic capture resolution of the lek paradox. Nat Comm 10:1359

    Article 

    Google Scholar
     

  • Falconer DS, Mackay TFC (1996) Introduction to quantitative genetics. Longman, Pearson Education, Essex

  • Griffith SC, Owens IPF, Burke T (1999) Environmental determination of a sexually selected trait. Nature 400:358–360

    Article 
    CAS 

    Google Scholar
     

  • Howie JM, Dawson HAC, Pomiankowski A, Fowler K (2019) Limits to environmental masking of genetic quality in sexual signals. J Evol Biol 32:868–877

    Article 
    PubMed 

    Google Scholar
     

  • Hunt J, Breuker CJ, Sadowski JA, Moore AJ (2008) Male-male competition, female mate choice and their interactions: determining total sexual selection. J Evol Biol 22:13–26

    Article 

    Google Scholar
     

  • Jensen H, Steinsland I, Ringsby TH, Sæther B-E (2008) Evolutionary dynamics of a sexual ornament in the house sparrow (Passer domesticus): the role of indirect selection within and between sexes. Evolution 62:1275–1293

    Article 
    PubMed 

    Google Scholar
     

  • Karino K, Haijima Y (2001) Heritability of male secondary sexual traits in feral guppies in Japan. J Ethol 19:33–37

    Article 

    Google Scholar
     

  • Kirkpatrick M, Ryan MJ (1991) The evolution of mating preferences and the paradox of the lek. Nature 350:33–38

    Article 

    Google Scholar
     

  • Kotiaho JS, Simmons LW, Tomkins JL (2001) Towards a resolution of the lek paradox. Nature 410:684–686

    Article 
    CAS 
    PubMed 

    Google Scholar
     

  • Kruuk LEB (2004) Estimating genetic parameters in natural populations using the ‘animal model’. Philos Trans R Soc Lond B 359:873–890

    Article 

    Google Scholar
     

  • Kruuk L, Hadfield J (2007) How to separate genetic and environmental causes of similarity between relatives. J Evol Biol 20:1890–1903

    Article 
    CAS 
    PubMed 

    Google Scholar
     

  • Le Galliard J-F, Ferrière R (2008) Evolution of maximal endurance capacity: natural and sexual selection across age classes in a lizard. Evol Ecol Res 10:157–176


    Google Scholar
     

  • Lindsay WR, Madsen T, Wapstra E, Lillie M, Loeb L, Ujvari B et al. (2020) Long term effects of outbreeding: experimental founding of island population eliminates malformations and improves hatching success in sand lizards. Biol Cons 249:108710

    Article 

    Google Scholar
     

  • Lindsay WR, Wapstra E, Silverin B, Olsson M(2016) Corticosterone: a costly mediator of signal honesty in sand lizards. Ecol Evol 6:7451–7461

    Article 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Lynch M, Walsh B (1998) Genetics and analysis of quantitative traits. Sinauer, Sunderland, MA

  • Martinossi-Allibert I, Rueffler C, Arnqvist G, Berger D (2018) The efficacy of sexual selection under environmental change. Preprint at Biorxiv:283457

  • Martins F, Kruuk L, Lewelyn J, Moritz C, Phillips B (2019) Heritability of climate-relevant traits in a rainforest skink. Heredity 122:41–52

    Article 
    PubMed 

    Google Scholar
     

  • Mentesana L, Isaksson C, Goymann W, Andersson MN, Trappschuh M, Hau M (2019) Female variance in allocation of steroid hormones, antioxidants and fatty acids: a multilevel analysis in a wild passerine bird. J Avian Biol 50:e01859

  • Merilä J, Kruuk L, Sheldon B (2001) Natural selection on the genetical component of variance in body condition in a wild bird population. J Evol Biol 14:918–929

    Article 

    Google Scholar
     

  • Merila J, Sheldon BC (1999) Genetic architecture of fitness and nonfitness traits: empirical patterns and development of ideas. Heredity 83:103–109

    Article 
    PubMed 

    Google Scholar
     

  • Mousseau TA, Fox CW (1998) The adaptive significance of maternal effects. Trends Ecol Evol 13:403–407

    Article 
    CAS 
    PubMed 

    Google Scholar
     

  • Noble DW, McFarlane SE, Keogh JS, Whiting MJ (2014) Maternal and additive genetic effects contribute to variance in offspring traits in a lizard. Behav Ecol 25:633–640

    Article 

    Google Scholar
     

  • Olsson M (1994a) Nuptial coloration in the sand lizard, Lacerta agilis: an intra-sexually selected cue to fighting ability. Anim Behav 48:607–613

    Article 

    Google Scholar
     

  • Olsson M (1994b) Why are sand lizard males (Lacerta agilis) not equally green? Behav Ecol Sociobiol 35:169–173

    Article 

    Google Scholar
     

  • Olsson M, Madsen T (2001) Promiscuity in sand lizards (Lacerta agilis) and adder snakes (Vipera berus): causes and consequences. J Hered 92:190–197

    Article 
    CAS 
    PubMed 

    Google Scholar
     

  • Olsson M, Madsen T, Wapstra E, Silverin B, Ujvari B, Wittzell H (2005) MHC, health, color, and reproductive success in sand lizards. Behav Ecol Sociobiol 58:289–294

    Article 

    Google Scholar
     

  • Olsson M, Shine R (1996) Does reproductive success increase with age or with size in a species with indeterminate growth? A case study using sand lizards Lacerta agilis. Oecologia 105:175–178

    Article 
    PubMed 

    Google Scholar
     

  • Olsson M, Wapstra E, Madsen T, Silverin B (2000) Testosterone, ticks and travels: a test of the immunocompetence-handicap hypothesis in free-ranging male sand lizards. Proc R Soc Lond B 267:2339–2343

    Article 
    CAS 

    Google Scholar
     

  • Olsson M, Wapstra E, Schwartz T, Madsen T, Ujvari B, Uller T (2011) In hot pursuit: fluctuating mating system and sexual selection in sand lizards. Evolution 65:574–583

    Article 
    PubMed 

    Google Scholar
     

  • Paranjpe DA, Bastiaans E, Patten A, Cooper RD, Sinervo B (2013) Evidence of maternal effects on temperature preference in side‐blotched lizards: implications for evolutionary response to climate change. Ecol Evol 3:1977–1991

    Article 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Pomiankowski A, Møller AP (1995) A resolution of the lek paradox. Proc R Soc Lond B 260:21–29

    Article 

    Google Scholar
     

  • Qvarnström A, Price TD (2001) Maternal effects, paternal effects and sexual selection. Trends Ecol Evol 16:95–100

    Article 
    PubMed 

    Google Scholar
     

  • Reeve HK, Pfennig DW (2003) Genetic biases for showy males: are some genetic systems especially conducive to sexual selection? Proc Nat Acad Sci USA 100:1089–1094

    Article 
    CAS 
    PubMed 
    PubMed Central 

    Google Scholar
     

  • Rowe L, Houle D (1996) The lek paradox and the capture of genetic variance by condition dependent traits. Proc R Soc Lond B 263:1415–1421

    Article 

    Google Scholar
     

  • Schielzeth H, Kempenaers B, Ellegren H, Forstmeier W (2012) QTL linkage mapping of zebra finch beak color shows an oligogenic control of a sexually selected trait. Evolution 66:18–30

    Article 
    PubMed 

    Google Scholar
     

  • Shine R, Harlow P (1993) Maternal thermoregulation influences offspring viability in a viviparous lizard. Oecologia 96:122–127

    Article 
    CAS 
    PubMed 

    Google Scholar
     

  • Singh A, Punzalan D (2018) The strength of sex‐specific selection in the wild. Evolution 72:2818–2824

    Article 
    PubMed 

    Google Scholar
     

  • Tibbetts EA (2010) The condition dependence and heritability of signaling and nonsignaling color traits in paper wasps. Am Nat 175:495–503

    Article 
    PubMed 

    Google Scholar
     

  • Tomkins JL, Radwan J, Kotiaho JS, Tregenza T (2004) Genic capture and resolving the lek paradox. Trends Ecol Evol 19:323–328

    Article 
    PubMed 

    Google Scholar
     

  • Van Homrigh A, Higgie M, McGuigan K, Blows MW (2007) The depletion of genetic variance by sexual selection. Curr Biol 17:528–532

    Article 
    PubMed 

    Google Scholar
     

  • Zakharov VM (1989) Future prospects for population phenogenetics. Sov Sci Rev Sect F Physiol Gen Biol Rev 4:1–79


    Google Scholar
     

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