in

Plastic female choice to optimally balance (k)in- and out-breeding in a predatory mite

  • 1.

    Wright, S. Evolution and the genetics of populations, vol 3: experimental results and evolutionary deductions. University of Chicago Press (1977).

  • 2.

    Charlesworth, D. & Charlesworth, B. Inbreeding depression and its evolutionary consequences. Annu Rev Ecol Syst. 18, 237–268 (1987).

    • Article
    • Google Scholar
  • 3.

    Fox, C. W. & Reed, D. H. Inbreeding depression increases with environmental stress: an experimental study and meta‐analysis. Evolution 65, 246–258 (2011).

  • 4.

    Bateson, P. Optimal outbreeding. Cambridge University Press (1983).

  • 5.

    Templeton, A. R. Coadaptation and outbreeding depression. In: Soulé ME, editor Conservation biology: the science of scarcity and diversity. Sunderland, Sinauer Associates. p. 105–116 (1986).

  • 6.

    Thornhill, N. W. The natural history of inbreeding and outbreeding: theoretical and empirical perspectives. University of Chicago Press (1993).

  • 7.

    Peer, K. & Taborsky, M. Outbreeding depression, but no inbreeding depression in haplodiploid ambrosia beetles with regular sibling mating. Evolution 59, 317–323 (2005).

  • 8.

    Kokko, H. & Ots, I. When not to avoid inbreeding. Evolution 60, 467–475 (2006).

  • 9.

    Puurtinen, M. Mate choice for optimal (k)inbreeding. Evolution 65, 1501–1505 (2011).

  • 10.

    Hamilton, W. D. The genetical evolution of social behavior I. J Theor Biol. 7, 1–16 (1964a).

  • 11.

    Hamilton, W. D. The genetical evolution of social behavior II. J Theor Biol. 7, 17–52 (1964b).

  • 12.

    Taylor, P. D. & Getz, W. M. An inclusive fitness model for the evolutionary advantage of sibmating. Evol Ecol. 8, 61–69 (1994).

    • Article
    • Google Scholar
  • 13.

    Szulkin, M., Stopher, K. V., Pemberton, J. M. & Reid, J. M. Inbreeding avoidance, tolerance, or preference in animals? Trends Ecol Evol. 28, 205–211 (2013).

  • 14.

    Waldman, B. The ecology of kin recognition. Annu Rev Ecol Syst. 19, 543–571 (1988).

    • Article
    • Google Scholar
  • 15.

    Sherman, P. W., Reeve, H. K. & Pfennig, D. W. Recognition Systems. In: Krebs J. R. & Davies N. B., editors. Behavioural Ecology: An Evolutionary Approach, 4th ed. Oxford, Blackwell Science. p. 69–96 (1997).

  • 16.

    Hepper, P. G. Kin recognition. Cambridge University Press (2005).

  • 17.

    Pusey, A. & Wolf, M. Inbreeding avoidance in animals. Trends Ecol Evol. 11, 201–206 (1996).

  • 18.

    Cheetham, S. A., Thom, M. D., Beynon, R. J. & Hurst, J. L. The effects of familiarity on mate choice. In: Hurst, J. L., Beynon, R. J., Roberts, S. C. & Wyatt, T. D. editors. Chemical Signals in Vertebrates 11. Heidelberg, Springer. p. 271–280 (2008).

  • 19.

    Clarke, F. M. & Faulkes, C. G. Kin discrimination and female mate choice in the naked mole-rat Heterocephalus glaber. Proc R Soc Lond B. 266, 1995–2002 (1999).

  • 20.

    Brandt, R. & Macdonald, B. W. To know him is to love him? Familiarity and female preference in the harvest mouse, Micromys minutus. Anim Behav. 82, 353–358 (2011).

    • Article
    • Google Scholar
  • 21.

    Bordogna, G. et al. An experimental test of relatedness-based mate discrimination in a social lizard. Behav Ecol Sociobiol. 70, 2139–2147 (2016).

    • Article
    • Google Scholar
  • 22.

    Thünken, T., Bakker, T. C. M., Baldauf, S. A. & Kullmann, H. Active inbreeding in a cichlid fish and its adaptive significance. Curr Biol. 17, 225–229 (2007).

  • 23.

    Robinson, S. P., Kennington, W. J. & Simmons, L. W. Assortative mating for relatedness in a large naturally occurring population of Drosophila melanogaster. J Evol Biol. 25, 716–725 (2012).

  • 24.

    Bateson, P. Preferences for cousins in Japanese quail. Nature 295, 236–237 (1982).

  • 25.

    Keane, B. The effect of relatedness on reproductive success and mate choice in the white-footed mouse, Peromyscus leucopus. Anim Behav. 39, 264–273 (1990).

    • Article
    • Google Scholar
  • 26.

    Richard, M., Losdat, S., Lecomte, J., de Fraipont, M. & Clobert, J. Optimal level of inbreeding in the common lizard. Proc R Soc Lond B. 276, 2779–2786 (2009).

  • 27.

    Atalay, D. & Schausberger, P. Balancing in- and out-breeding by the predatory mite Phytoseiulus persimilis. Exp Appl Acarol. 74, 159–169 (2018).

  • 28.

    Schausberger, P. et al. Ultimate drivers and proximate correlates of polyandry in predatory mites. PloS ONE 11, e0154355 (2016).

  • 29.

    Schausberger, P., Walzer, A., Murata, Y. & Osakabe, M. Low level of polyandry constrains phenotypic plasticity of male body size in mites. PLoS ONE 12, e0188924 (2017).

  • 30.

    Sabelis, M. W. Reproductive strategies. In: Helle, W. & Sabelis, M. W. editors. Spider mites, their biology, natural enemies and control, vol 1A. Amsterdam, Elsevier. p. 265–278 (1985).

  • 31.

    McMurtry, J. A. & Croft, B. A. Life-styles of phytoseiid mites and their roles in biological control. Annu Rev Entomol. 42, 291–321 (1997).

  • 32.

    Schausberger, P. & Croft, B. A. Kin recognition and larval cannibalism by adult females in specialist predaceous mites. Anim Behav. 61, 459–464 (2001).

    • Article
    • Google Scholar
  • 33.

    Enigl, M. & Schausberger, P. Mate choice in the predaceous mite Phytoseiulus persimilis: evidence of self-referent phenotype matching? Entomol Exp Appl. 112, 21–28 (2004).

    • Article
    • Google Scholar
  • 34.

    Schausberger, P. Ontogenetic isolation favours sibling cannibalism in mites. Anim Behav. 67, 1031–1035 (2004).

    • Article
    • Google Scholar
  • 35.

    Schausberger, P. The predatory mite Phytoseiulus persimilis manipulates imprinting among offspring through egg placement. Behav Ecol Sociobiol. 58, 53–59 (2005).

    • Article
    • Google Scholar
  • 36.

    Schausberger, P. Kin recognition by juvenile predatory mites: prior association or phenotype matching? Behav Ecol Sociobiol. 62, 119–125 (2007).

    • Article
    • Google Scholar
  • 37.

    Schausberger P., Gratzer M. & Strodl M. A. Early social isolation impairs development, mate choice and grouping behavior of predatory mites. Anim Behav. 127, 15–21 (2017).

  • 38.

    Sabelis, M. W. & Dicke, M. Long range dispersal and searching behaviour. In: Helle, W. & Sabelis, M. W. editors. Spider mites, their biology, natural enemies and control, vol 1B. Amsterdam, Elsevier. p. 141–160 (1985).

  • 39.

    Blaustein, A. R. & Porter, R. H. The ubiquitous concept of recognition with special reference to kin. In: Bekoff, M. & Jamieson, D. editors. Readings in Animal Cognition. Cambridge, MIT Press. p. 169–184 (1996).

  • 40.

    Porter, R. H. The ontogeny of sibling recognition in rodents: Superfamily Muroidea. Behav Genet. 18, 483–494 (1988).

  • 41.

    De Moraes, G. J., McMurtry, J. A., Denmark, H. A. & Campos, C. B. A revised catalogue of the mite family Phytoseiidae. Zootaxa 434, 1–494 (2004).

    • Article
    • Google Scholar
  • 42.

    Schausberger, P. Inter-and intraspecific predation on immatures by adult females in Euseius finlandicus, Typhlodromus pyri and Kampimodromus aberrans (Acari: Phytoseiidae). Exp Appl Acarol. 21, 131–150 (1997).

    • Article
    • Google Scholar
  • 43.

    Amano, H. & Chant, D. A. Mating behaviour and reproductive mechanisms of two species of predacious mites, Phytoseiulus persimilis Athias-Henriot and Amblyseius andersoni (Chant) (Acarina: Phytoseiidae). Acarologia 20, 196–213 (1978).

    • Google Scholar
  • 44.

    Reeve, H. K. The evolution of conspecific acceptance thresholds. Am Nat. 133, 407–435 (1989).

    • Article
    • Google Scholar
  • 45.

    Schausberger, P. Taking care of group size and heterogeneity in social recognition systems. Behav Ecol Sociobiol. 68, 1261–1562 (2014).

    • Article
    • Google Scholar
  • 46.

    Bolhuis, J. J., Strijkstra, A. M., Moor, E. & van der Lende, K. Preferences for odours of conspecific non-siblings in the common vole, Microtus arvalis. Anim Behav. 36, 1551–1553 (1988).

    • Article
    • Google Scholar
  • 47.

    Simmons, L. W. Female choice and the relatedness of mates in the field cricket, Gryllus bimaculatus. Anim Behav. 41, 493–501 (1991).

    • Article
    • Google Scholar
  • 48.

    Keller, L. & Passera, L. Incest avoidance, fluctuating asymmetry, and the consequences of inbreeding in Iridomyrmex humilis, an ant with multiple queen colonies. Behav Ecol Sociobiol. 33, 191–199 (1993).

    • Article
    • Google Scholar
  • 49.

    Shellman-Reeve, J. S. Genetic relatedness and partner preference in a monogamous, wood-dwelling termite. Anim Behav. 61, 869–876 (2001).

    • Article
    • Google Scholar
  • 50.

    Çekin, D. & Schausberger, P. Founder effects on trans-generational dynamics of closed inbreeding lineages of the predatory mite Phytoseiulus persimilis. PLoS ONE 14, e0215360 (2019).

  • 51.

    Arbuthnott, D., Fedina, T. Y., Pletcher, S. D. & Promislow, D. E. L. Mate choice in fruit flies is rational and adaptive. Nat Commun. 8, 13953 (2017).


  • Source: Ecology - nature.com

    3 Questions: Harnessing wave power to rebuild islands

    Climate knowledge for everyone