Lifetime monogamy and the evolution of eusociality

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Lifetime monogamy and the evolution of eusociality. / Boomsma, Jacobus J.

I: Philosophical Transactions of the Royal Society of London. Biological Sciences, Bind 364, Nr. 1533, 2009, s. 3191-207.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Boomsma, JJ 2009, 'Lifetime monogamy and the evolution of eusociality', Philosophical Transactions of the Royal Society of London. Biological Sciences, bind 364, nr. 1533, s. 3191-207. https://doi.org/10.1098/rstb.2009.0101

APA

Boomsma, J. J. (2009). Lifetime monogamy and the evolution of eusociality. Philosophical Transactions of the Royal Society of London. Biological Sciences, 364(1533), 3191-207. https://doi.org/10.1098/rstb.2009.0101

Vancouver

Boomsma JJ. Lifetime monogamy and the evolution of eusociality. Philosophical Transactions of the Royal Society of London. Biological Sciences. 2009;364(1533):3191-207. https://doi.org/10.1098/rstb.2009.0101

Author

Boomsma, Jacobus J. / Lifetime monogamy and the evolution of eusociality. I: Philosophical Transactions of the Royal Society of London. Biological Sciences. 2009 ; Bind 364, Nr. 1533. s. 3191-207.

Bibtex

@article{fbe39280285911df8ed1000ea68e967b,
title = "Lifetime monogamy and the evolution of eusociality",
abstract = "All evidence currently available indicates that obligatory sterile eusocial castes only arose via the association of lifetime monogamous parents and offspring. This is consistent with Hamilton's rule (br(s) > r(o)c), but implies that relatedness cancels out of the equation because average relatedness to siblings (r(s)) and offspring (r(o)) are both predictably 0.5. This equality implies that any infinitesimally small benefit of helping at the maternal nest (b), relative to the cost in personal reproduction (c) that persists throughout the lifespan of entire cohorts of helpers suffices to establish permanent eusociality, so that group benefits can increase gradually during, but mostly after the transition. The monogamy window can be conceptualized as a singularity comparable with the single zygote commitment of gametes in eukaryotes. The increase of colony size in ants, bees, wasps and termites is thus analogous to the evolution of multicellularity. Focusing on lifetime monogamy as a universal precondition for the evolution of obligate eusociality simplifies the theory and may help to resolve controversies about levels of selection and targets of adaptation. The monogamy window underlines that cooperative breeding and eusociality are different domains of social evolution, characterized by different sectors of parameter space for Hamilton's rule.",
author = "Boomsma, {Jacobus J}",
note = "Keywords: Animals; Evolution; Hymenoptera; Selection, Genetic; Sexual Behavior, Animal; Social Behavior",
year = "2009",
doi = "10.1098/rstb.2009.0101",
language = "English",
volume = "364",
pages = "3191--207",
journal = "Philosophical Transactions of the Royal Society B: Biological Sciences",
issn = "0962-8436",
publisher = "The/Royal Society",
number = "1533",

}

RIS

TY - JOUR

T1 - Lifetime monogamy and the evolution of eusociality

AU - Boomsma, Jacobus J

N1 - Keywords: Animals; Evolution; Hymenoptera; Selection, Genetic; Sexual Behavior, Animal; Social Behavior

PY - 2009

Y1 - 2009

N2 - All evidence currently available indicates that obligatory sterile eusocial castes only arose via the association of lifetime monogamous parents and offspring. This is consistent with Hamilton's rule (br(s) > r(o)c), but implies that relatedness cancels out of the equation because average relatedness to siblings (r(s)) and offspring (r(o)) are both predictably 0.5. This equality implies that any infinitesimally small benefit of helping at the maternal nest (b), relative to the cost in personal reproduction (c) that persists throughout the lifespan of entire cohorts of helpers suffices to establish permanent eusociality, so that group benefits can increase gradually during, but mostly after the transition. The monogamy window can be conceptualized as a singularity comparable with the single zygote commitment of gametes in eukaryotes. The increase of colony size in ants, bees, wasps and termites is thus analogous to the evolution of multicellularity. Focusing on lifetime monogamy as a universal precondition for the evolution of obligate eusociality simplifies the theory and may help to resolve controversies about levels of selection and targets of adaptation. The monogamy window underlines that cooperative breeding and eusociality are different domains of social evolution, characterized by different sectors of parameter space for Hamilton's rule.

AB - All evidence currently available indicates that obligatory sterile eusocial castes only arose via the association of lifetime monogamous parents and offspring. This is consistent with Hamilton's rule (br(s) > r(o)c), but implies that relatedness cancels out of the equation because average relatedness to siblings (r(s)) and offspring (r(o)) are both predictably 0.5. This equality implies that any infinitesimally small benefit of helping at the maternal nest (b), relative to the cost in personal reproduction (c) that persists throughout the lifespan of entire cohorts of helpers suffices to establish permanent eusociality, so that group benefits can increase gradually during, but mostly after the transition. The monogamy window can be conceptualized as a singularity comparable with the single zygote commitment of gametes in eukaryotes. The increase of colony size in ants, bees, wasps and termites is thus analogous to the evolution of multicellularity. Focusing on lifetime monogamy as a universal precondition for the evolution of obligate eusociality simplifies the theory and may help to resolve controversies about levels of selection and targets of adaptation. The monogamy window underlines that cooperative breeding and eusociality are different domains of social evolution, characterized by different sectors of parameter space for Hamilton's rule.

U2 - 10.1098/rstb.2009.0101

DO - 10.1098/rstb.2009.0101

M3 - Journal article

C2 - 19805427

VL - 364

SP - 3191

EP - 3207

JO - Philosophical Transactions of the Royal Society B: Biological Sciences

JF - Philosophical Transactions of the Royal Society B: Biological Sciences

SN - 0962-8436

IS - 1533

ER -

ID: 18389871