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[[File:White-headed marmoset.jpg|thumb|White-headed marmoset]]
[[File:White-headed marmoset.jpg|thumb|White-headed marmoset]]
'''Reproductive Suppression''' involves the prevention or inhibition of [[reproduction]] in otherwise healthy adult individuals.<ref name=ref1>{{cite journal | last1 = Wasser | first1 = S.K. | last2 = Barash | first2 = D.P | year = 1983 | title = Reproductive suppression among female mammals: implicaitons for biomedicine and sexual selection theory | url = | journal = The Quarterly Review of Biology | volume = 58 | issue = | pages = 513–538 }} Quote is from p. 513.</ref> It includes delayed sexual maturation ([[puberty]]) or inhibition of sexual receptivity, facultatively increased interbirth interval through delayed or inhibited [[ovulation]] or spontaneous or induced abortion, abandonment of immature and dependent offspring, mate guarding, selective destruction and [[worker policing]] of eggs in some [[Eusociality|eusocial]] insects or cooperatively breeding birds, and [[infanticide]] (see also [[infanticide (zoology)]]), and [[infanticide in carnivores]]) of the offspring of subordinate females either by directly killing by dominant females or males in mammals or indirectly through the withholding of assistance with infant care in [[marmoset]]s and some carnivores.<ref name=ref2>Saltzman, W., Leidl, K.J., Salper, O.J., Pick, R.R., Abbott, D.H. (2008) Hormones and Behavior 53: 274-286.</ref><ref name=ref3>{{cite journal | last1 = Saltzman | first1 = W. | last2 = Digby | first2 = L.J. | last3 = Abbott | first3 = D.H. | year = 2009 | title = Reproductive skew in female common marmosets: what can proximate mechanisms tell us about ultimate causes | url = | journal = Proceedings of the Royal Society B | volume = 276 | issue = | pages = 389–399 }}</ref>
'''Reproductive Suppression''' involves the prevention or inhibition of [[reproduction]] in otherwise healthy adult individuals.<ref name=ref1>{{cite journal | last1 = Wasser | first1 = S.K. | last2 = Barash | first2 = D.P | year = 1983 | title = Reproductive suppression among female mammals: implicaitons for biomedicine and sexual selection theory | url = | journal = The Quarterly Review of Biology | volume = 58 | issue = | pages = 513–538 | doi=10.1086/413545}} Quote is from p. 513.</ref> It includes delayed sexual maturation ([[puberty]]) or inhibition of sexual receptivity, facultatively increased interbirth interval through delayed or inhibited [[ovulation]] or spontaneous or induced abortion, abandonment of immature and dependent offspring, mate guarding, selective destruction and [[worker policing]] of eggs in some [[Eusociality|eusocial]] insects or cooperatively breeding birds, and [[infanticide]] (see also [[infanticide (zoology)]]), and [[infanticide in carnivores]]) of the offspring of subordinate females either by directly killing by dominant females or males in mammals or indirectly through the withholding of assistance with infant care in [[marmoset]]s and some carnivores.<ref name=ref2>Saltzman, W., Leidl, K.J., Salper, O.J., Pick, R.R., Abbott, D.H. (2008) Hormones and Behavior 53: 274-286.</ref><ref name=ref3>{{cite journal | last1 = Saltzman | first1 = W. | last2 = Digby | first2 = L.J. | last3 = Abbott | first3 = D.H. | year = 2009 | title = Reproductive skew in female common marmosets: what can proximate mechanisms tell us about ultimate causes | url = | journal = Proceedings of the Royal Society B | volume = 276 | issue = | pages = 389–399 | doi=10.1098/rspb.2008.1374}}</ref>
The ''Reproductive Suppression Model'' argues that “females can optimize their lifetime [[reproductive success]] by suppressing reproduction when future [physical or social] conditions for the survival of offspring are likely to be greatly improved over present ones”.<ref name=ref1 /> When intragroup competition (competition between individuals belonging to the same group) is high it may be beneficial to suppress the reproduction of others, and for subordinate females to suppress their own reproduction until a later time when social competition is reduced. This leads to reproductive skew within a social group, with some individuals having more offspring than others. The cost of reproductive suppression to the individual is lowest at the earliest stages of a reproductive event and reproductive suppression is often easiest to induce at the pre-ovulatory or earliest stages of pregnancy in mammals, and greatest after a birth. Therefore, [[Neuroendocrinology|neuroendocrine]] cues for assessing reproductive success should evolve to be reliable at early stages in the ovulatory cycle.
The ''Reproductive Suppression Model'' argues that “females can optimize their lifetime [[reproductive success]] by suppressing reproduction when future [physical or social] conditions for the survival of offspring are likely to be greatly improved over present ones”.<ref name=ref1 /> When intragroup competition (competition between individuals belonging to the same group) is high it may be beneficial to suppress the reproduction of others, and for subordinate females to suppress their own reproduction until a later time when social competition is reduced. This leads to reproductive skew within a social group, with some individuals having more offspring than others. The cost of reproductive suppression to the individual is lowest at the earliest stages of a reproductive event and reproductive suppression is often easiest to induce at the pre-ovulatory or earliest stages of pregnancy in mammals, and greatest after a birth. Therefore, [[Neuroendocrinology|neuroendocrine]] cues for assessing reproductive success should evolve to be reliable at early stages in the ovulatory cycle.
Reproductive suppression occurs in its most extreme form in eusocial insects such as termites, hornets and bees and the mammalian naked mole rat which depend on a complex division of labor within the group for survival and in which specific genes, epigenetics and other factors are known to determine whether individuals will permanently be unable to breed or able to reach reproductive maturity under particular social conditions,<ref name=ref4>{{cite journal | last1 = Korb | first1 = J. | last2 = Weil | first2 = T. | last3 = Hoffman | first3 = K. | last4 = Foster | first4 = K.R. | last5 = Rehli | first5 = M. | year = 2009 | title = A gene necessary for reproductive suppression in termites | url = | journal = Science | volume = 324 | issue = | page = 758 }}</ref><ref name=ref5>Jarosch, A., Stole, E., Crewe, R.., and Moritz, R.F.A. (2011) Alternative splicing of a single transcription factor drives selfish reproductive behavior in honeybee workers (''Apis mellifera'') (2011) Proceedings of the National Academy of Sciences – 108: 15282–15287.</ref><ref name=ref6>{{cite journal | last1 = Faulkes | first1 = C.G. | last2 = Bennet | first2 = N.C. | year = 2001 | title = Family values: group dynamics and social control of reproduction in African mole-rates | url = | journal = Trends in Ecology and Evolution | volume = 16 | issue = 4| pages = 184–190 }}</ref> and cooperatively breeding fish, birds and mammals in which a breeding pair depends on helpers whose reproduction is suppressed for the survival of their own offspring.<ref name=ref7>{{cite journal | last1 = Koenig | first1 = W.D. | last2 = Mumme | first2 = R.L. | last3 = Stanback | first3 = | last4 = Pitelka | first4 = F.A. | year = 1995 | title = Patterns and consequences of egg destruction among joint-nesting acorn woodpeckers | url = | journal = Animal Behaviour | volume = 50 | issue = | pages = 607–621 }}</ref><ref name=ref8>{{cite journal | last1 = Hradecky | first1 = P | year = 1985 | title = Possible pheromonal regulation of reproduction in wild carnivores | url = | journal = Journal of Chemical Ecology | volume = 11 | issue = | pages = 241–250 }}</ref><ref name=ref9>{{cite journal | last1 = Creel | first1 = S.R. | last2 = Creel | first2 = N.M. | year = 1991 | title = Energetics, reproductive suppression and obligate communal breeding in carnivores | url = | journal = Behavioral Ecology and Sociobiology | volume = 28 | issue = | pages = 263–270 }}</ref><ref name=ref10>{{cite journal | last1 = Doolan | first1 = S.P. | last2 = MacDonald | first2 = D.W. | year = 1997 | title = Band structure and failures of reproductive suppression in a cooperatively breeding carnivore, the slender-tailed meerkat (''Suricata suricatta'') | url = | journal = Behaviour | volume = 134 | issue = | pages = 827–848 }}</ref><ref name=ref11>{{cite journal | last1 = Garber | first1 = P.A. | year = 1997 | title = One for all and breeding for one: cooperation and competition as a tamarin reproductive strategy | url = | journal = Evolutionary Anthropology | volume = 5 | issue = | pages = 187–199 }}</ref><ref name=ref12>{{cite journal | last1 = Clutton-Brock | first1 = T.H. | last2 = Brotherton | first2 = P.N.M. | last3 = Smith | first3 = R. McIlrath G. | last4 = Kansky | first4 = R. | last5 = Gaynor | first5 = D. | last6 = O'Riain | first6 = M.J. | last7 = Skinner | first7 = J.D. | year = 1998 | title = Infanticide and expulsion of females in a cooperative mammal | url = | journal = Proceedings Royal Society of London Ser B Biological Science | volume = 265 | issue = | pages = 2291–2295 }}</ref><ref name=ref13>{{cite journal | last1 = Cant | first1 = M.A. | year = 2000 | title = Social control of reproduction in banded mongooses | url = | journal = Animal Behaviour | volume = 59 | issue = | pages = 147–158 }}</ref><ref name=ref14>{{cite journal | last1 = Young | first1 = A.J. | last2 = Carlson | first2 = A.A. | last3 = Monfort | first3 = S.L. | last4 = Russell | first4 = A. F. | last5 = Bennett | first5 = N.C. | last6 = Clutton-Brock | first6 = T. | year = 2005 | title = Stress and the suppression of subordinate reproduction in cooperatively breeding meerkats | url = | journal = Proceedings of the National Academy of Sciences | volume = 103 | issue = | pages = 12005–12010 }}</ref><ref name=ref15>Spiering, P.A., Somers, M.J., Maldonado, J.E., Wildt, D.E., Gunter, M.S. (2010) Reproductive sharing and proximate factors mediating cooperative breeding in the African wild dog (Lycaon pictus) Behavioral Ecology Sociobiology 64:583–592.</ref><ref name=ref16>{{cite journal | last1 = Schradin | first1 = C. | last2 = Pillay | first2 = N. | year = 2014 | title = Absence of reproductive suppression in young adult female striped mice living in their natal family | url = | journal = Animal Behaviour | volume = 90 | issue = | pages = 141–148 }}</ref> In eusocial and cooperatively breeding animals most non-reproducing helpers engage in kin selection, enhancing their own inclusive fitness by ensuring the survival of offspring they are closely related to.<ref name=ref17>{{cite journal | last1 = Hamilton | first1 = WD | year = 1964 | title = The genetical evolution of social behaviour. I | url = | journal = Journal of Theoretical Biology: | volume = 7 | issue = | pages = 1–16 }}</ref> Wolf packs suppress subordinate breeding.
Reproductive suppression occurs in its most extreme form in eusocial insects such as termites, hornets and bees and the mammalian naked mole rat which depend on a complex division of labor within the group for survival and in which specific genes, epigenetics and other factors are known to determine whether individuals will permanently be unable to breed or able to reach reproductive maturity under particular social conditions,<ref name=ref4>{{cite journal | last1 = Korb | first1 = J. | last2 = Weil | first2 = T. | last3 = Hoffman | first3 = K. | last4 = Foster | first4 = K.R. | last5 = Rehli | first5 = M. | year = 2009 | title = A gene necessary for reproductive suppression in termites | url = | journal = Science | volume = 324 | issue = | page = 758 | doi=10.1126/science.1170660}}</ref><ref name=ref5>Jarosch, A., Stole, E., Crewe, R.., and Moritz, R.F.A. (2011) Alternative splicing of a single transcription factor drives selfish reproductive behavior in honeybee workers (''Apis mellifera'') (2011) Proceedings of the National Academy of Sciences – 108: 15282–15287.</ref><ref name=ref6>{{cite journal | last1 = Faulkes | first1 = C.G. | last2 = Bennet | first2 = N.C. | year = 2001 | title = Family values: group dynamics and social control of reproduction in African mole-rates | url = | journal = Trends in Ecology and Evolution | volume = 16 | issue = 4| pages = 184–190 | doi=10.1016/s0169-5347(01)02116-4}}</ref> and cooperatively breeding fish, birds and mammals in which a breeding pair depends on helpers whose reproduction is suppressed for the survival of their own offspring.<ref name=ref7>{{cite journal | last1 = Koenig | first1 = W.D. | last2 = Mumme | first2 = R.L. | last3 = Stanback | first3 = | last4 = Pitelka | first4 = F.A. | year = 1995 | title = Patterns and consequences of egg destruction among joint-nesting acorn woodpeckers | url = | journal = Animal Behaviour | volume = 50 | issue = | pages = 607–621 | doi=10.1016/0003-3472(95)80123-5}}</ref><ref name=ref8>{{cite journal | last1 = Hradecky | first1 = P | year = 1985 | title = Possible pheromonal regulation of reproduction in wild carnivores | url = | journal = Journal of Chemical Ecology | volume = 11 | issue = | pages = 241–250 }}</ref><ref name=ref9>{{cite journal | last1 = Creel | first1 = S.R. | last2 = Creel | first2 = N.M. | year = 1991 | title = Energetics, reproductive suppression and obligate communal breeding in carnivores | url = | journal = Behavioral Ecology and Sociobiology | volume = 28 | issue = | pages = 263–270 | doi=10.1007/bf00175099}}</ref><ref name=ref10>{{cite journal | last1 = Doolan | first1 = S.P. | last2 = MacDonald | first2 = D.W. | year = 1997 | title = Band structure and failures of reproductive suppression in a cooperatively breeding carnivore, the slender-tailed meerkat (''Suricata suricatta'') | url = | journal = Behaviour | volume = 134 | issue = | pages = 827–848 | doi=10.1163/156853997x00179}}</ref><ref name=ref11>{{cite journal | last1 = Garber | first1 = P.A. | year = 1997 | title = One for all and breeding for one: cooperation and competition as a tamarin reproductive strategy | url = | journal = Evolutionary Anthropology | volume = 5 | issue = | pages = 187–199 | doi=10.1002/(sici)1520-6505(1997)5:6<187::aid-evan1>3.0.co;2-a}}</ref><ref name=ref12>{{cite journal | last1 = Clutton-Brock | first1 = T.H. | last2 = Brotherton | first2 = P.N.M. | last3 = Smith | first3 = R. McIlrath G. | last4 = Kansky | first4 = R. | last5 = Gaynor | first5 = D. | last6 = O'Riain | first6 = M.J. | last7 = Skinner | first7 = J.D. | year = 1998 | title = Infanticide and expulsion of females in a cooperative mammal | url = | journal = Proceedings Royal Society of London Ser B Biological Science | volume = 265 | issue = | pages = 2291–2295 | doi=10.1098/rspb.1998.0573}}</ref><ref name=ref13>{{cite journal | last1 = Cant | first1 = M.A. | year = 2000 | title = Social control of reproduction in banded mongooses | url = | journal = Animal Behaviour | volume = 59 | issue = | pages = 147–158 | doi=10.1006/anbe.1999.1279}}</ref><ref name=ref14>{{cite journal | last1 = Young | first1 = A.J. | last2 = Carlson | first2 = A.A. | last3 = Monfort | first3 = S.L. | last4 = Russell | first4 = A. F. | last5 = Bennett | first5 = N.C. | last6 = Clutton-Brock | first6 = T. | year = 2005 | title = Stress and the suppression of subordinate reproduction in cooperatively breeding meerkats | url = | journal = Proceedings of the National Academy of Sciences | volume = 103 | issue = | pages = 12005–12010 | doi=10.1073/pnas.0510038103}}</ref><ref name=ref15>Spiering, P.A., Somers, M.J., Maldonado, J.E., Wildt, D.E., Gunter, M.S. (2010) Reproductive sharing and proximate factors mediating cooperative breeding in the African wild dog (Lycaon pictus) Behavioral Ecology Sociobiology 64:583–592.</ref><ref name=ref16>{{cite journal | last1 = Schradin | first1 = C. | last2 = Pillay | first2 = N. | year = 2014 | title = Absence of reproductive suppression in young adult female striped mice living in their natal family | url = | journal = Animal Behaviour | volume = 90 | issue = | pages = 141–148 | doi=10.1016/j.anbehav.2014.01.029}}</ref> In eusocial and cooperatively breeding animals most non-reproducing helpers engage in kin selection, enhancing their own inclusive fitness by ensuring the survival of offspring they are closely related to.<ref name=ref17>{{cite journal | last1 = Hamilton | first1 = WD | year = 1964 | title = The genetical evolution of social behaviour. I | url = | journal = Journal of Theoretical Biology: | volume = 7 | issue = | pages = 1–16 | doi=10.1016/0022-5193(64)90038-4}}</ref> Wolf packs suppress subordinate breeding.


==Pre-fertilization mechanisms of reproductive suppression==
==Pre-fertilization mechanisms of reproductive suppression==
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====Food Shortages (resource availability)====
====Food Shortages (resource availability)====
Female mammals experience delays in the onset of puberty or increase their interbirth intervals in response to environmental conditions that are associated with low abundance and poor quality of foods. Nutritional stress is apparently linked to the female endocrine system and ovulatory [[Pheromone|pheromonal]] cycle. For example, [[Orangutan]]s (Pongo pygmaeus'') experience high [[ketone]] (due to fat burning) and low [[estrogen]] levels during times of low food availability and poor food quality, but low ketone and high estrogen levels that stimulates onset of the ovulation during the fruit masting seasons that occurs about every four years on Sumatra.<ref name=ref18>Knott, Cheryl 1998 Orangutans in the wild. National Geographic August 1998. http://www.timlaman.com/#/national-geographic-articles/98Aug-Orangutans</ref>[18] Since adult female orangutans are solitary, interference by other females can be ruled out as influencing their temporary reproductive suppression and facultatively long interbirth intervals. [[Polygynandrous]] [[yellow baboon]]s (''Papio cynocephalus) in Kenya were far less likely to ovulate or conceive during periods of drought or extreme heat, especially if they live in large groups, resulting in longer interbirth intervals during periods of nutritional and thermal stress.<ref name=ref19>{{cite journal | last1 = Beehner | first1 = J.C. | last2 = Onderdonk | first2 = D.A. | last3 = Alberts | first3 = S.C. | last4 = Altmann | first4 = J. | year = 2006 | title = The ecology of conception and pregnancy failure in wild baboons | url = | journal = Behavioral Ecology | volume = 17 | issue = | pages = 741–750 }}</ref><ref name=ref20>{{cite journal | last1 = Beehner | first1 = J.C. | last2 = Lu | first2 = A. | year = 2013 | title = Reproductive suppression in female primates: a review | url = | journal = Evolutionary Anthropology | volume = 22 | issue = | pages = 226–238 }}</ref>
Female mammals experience delays in the onset of puberty or increase their interbirth intervals in response to environmental conditions that are associated with low abundance and poor quality of foods. Nutritional stress is apparently linked to the female endocrine system and ovulatory [[Pheromone|pheromonal]] cycle. For example, [[Orangutan]]s (Pongo pygmaeus'') experience high [[ketone]] (due to fat burning) and low [[estrogen]] levels during times of low food availability and poor food quality, but low ketone and high estrogen levels that stimulates onset of the ovulation during the fruit masting seasons that occurs about every four years on Sumatra.<ref name=ref18>Knott, Cheryl 1998 Orangutans in the wild. National Geographic August 1998. http://www.timlaman.com/#/national-geographic-articles/98Aug-Orangutans</ref>[18] Since adult female orangutans are solitary, interference by other females can be ruled out as influencing their temporary reproductive suppression and facultatively long interbirth intervals. [[Polygynandrous]] [[yellow baboon]]s (''Papio cynocephalus) in Kenya were far less likely to ovulate or conceive during periods of drought or extreme heat, especially if they live in large groups, resulting in longer interbirth intervals during periods of nutritional and thermal stress.<ref name=ref19>{{cite journal | last1 = Beehner | first1 = J.C. | last2 = Onderdonk | first2 = D.A. | last3 = Alberts | first3 = S.C. | last4 = Altmann | first4 = J. | year = 2006 | title = The ecology of conception and pregnancy failure in wild baboons | url = | journal = Behavioral Ecology | volume = 17 | issue = | pages = 741–750 | doi=10.1093/beheco/arl006}}</ref><ref name=ref20>{{cite journal | last1 = Beehner | first1 = J.C. | last2 = Lu | first2 = A. | year = 2013 | title = Reproductive suppression in female primates: a review | url = | journal = Evolutionary Anthropology | volume = 22 | issue = | pages = 226–238 | doi=10.1002/evan.21369}}</ref>


====High population density====
====High population density====
High population density is one of the environmental factors that can lead to reproductive suppression. When population density is high, subordinate individuals may experience reproductive suppression that they would not have experiences otherwise. For example, when high numbers of yellow baboon (Papio cynocephalus) females are simultaneously in estrous at Mikumi National Park, Tanzania dominant females form coalitions that attack subordinate females, leading to a disruption in their reproductive cycle and failure to conceive.<ref name=ref1 /> This places constraints on the number of offspring born in a single generation. Since infant mortality in Amboseli yellow baboons depends in part on the number and ages of other infants born into the group, pre-ovulatory females that are most susceptible to stress-induced delay or inhibition of ovulation are the most frequent targets of female coalition attacks. Female attackers are often in advanced stages of pregnancy, and have the most to lose if the number of infants in the group reaches an unsustainable level. A similar study of [[Chacma baboon]]s (''Papio ursinus'') noted high levels of female-female aggression around the mating season when the number of ovulating females was high (indicated by sexual swellings) and that aggression directed toward suppressing the mating opportunities of ovulating females.<ref name=ref21>{{cite journal | last1 = Huchard | first1 = E. | last2 = Cowlishaw | first2 = G. | year = 2011 | title = Female-female aggression around mating: an extra cost of sociality in a multimale primate society | url = | journal = Behavioral Ecology | volume = 22 | issue = 5| pages = 1003–1011 }}</ref>
High population density is one of the environmental factors that can lead to reproductive suppression. When population density is high, subordinate individuals may experience reproductive suppression that they would not have experiences otherwise. For example, when high numbers of yellow baboon (Papio cynocephalus) females are simultaneously in estrous at Mikumi National Park, Tanzania dominant females form coalitions that attack subordinate females, leading to a disruption in their reproductive cycle and failure to conceive.<ref name=ref1 /> This places constraints on the number of offspring born in a single generation. Since infant mortality in Amboseli yellow baboons depends in part on the number and ages of other infants born into the group, pre-ovulatory females that are most susceptible to stress-induced delay or inhibition of ovulation are the most frequent targets of female coalition attacks. Female attackers are often in advanced stages of pregnancy, and have the most to lose if the number of infants in the group reaches an unsustainable level. A similar study of [[Chacma baboon]]s (''Papio ursinus'') noted high levels of female-female aggression around the mating season when the number of ovulating females was high (indicated by sexual swellings) and that aggression directed toward suppressing the mating opportunities of ovulating females.<ref name=ref21>{{cite journal | last1 = Huchard | first1 = E. | last2 = Cowlishaw | first2 = G. | year = 2011 | title = Female-female aggression around mating: an extra cost of sociality in a multimale primate society | url = | journal = Behavioral Ecology | volume = 22 | issue = 5| pages = 1003–1011 | doi=10.1093/beheco/arr083}}</ref>
Among [[elephant seal]]s (Mirounga) high neonatal mortality occurs when the number of pups born in a season is high, with deaths resulting from injury and starvation.<ref name=ref1 /> To counteract loss of their pups elephant seals conceive next year’s offspring immediately after giving birth to this year’s young, but delay implantation for 4 months. Female striped mice (Rhabdomys pumilio) in monogamous social groups do not experience reproductive suppression, but those living in communally breeding groups with high population density and large numbers of old breeding females do.<ref name=ref16 />
Among [[elephant seal]]s (Mirounga) high neonatal mortality occurs when the number of pups born in a season is high, with deaths resulting from injury and starvation.<ref name=ref1 /> To counteract loss of their pups elephant seals conceive next year’s offspring immediately after giving birth to this year’s young, but delay implantation for 4 months. Female striped mice (Rhabdomys pumilio) in monogamous social groups do not experience reproductive suppression, but those living in communally breeding groups with high population density and large numbers of old breeding females do.<ref name=ref16 />


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====Stress induced by aggression from dominant to subordinate individuals====
====Stress induced by aggression from dominant to subordinate individuals====
Chronic physiological stress resulting from aggression by dominant toward subordinate individuals is thought to be a major cause of delayed maturation and suppressed ovulation in subordinate individuals of a wide range of species.<ref name=ref14 /><ref name=ref22>{{cite journal | last1 = Bowman | first1 = L. | last2 = Dilley | first2 = S.R. | last3 = Keverne | first3 = E.B. | year = 1978 | title = Supression of oestrogen-induced LH surges by social subordination in talapoin monkeys | url = | journal = Nature | volume = 275 | issue = | pages = 56–58 }}</ref><ref name=ref23>Arnold, W. & Dittami, J. (1997) Reproductive suppression in male alpine marmots Animal Behaviour 53: 53–66.</ref><ref name=ref24>Hacklander, K., Mostl, E, Arnold, W. (2003) Reproductive suppression in female Alpine marmots (Marmota marmot) Animal Behavior 65: 1133-1140.</ref> In response to stress the HPA axis (hypothalamic-pituitary-adrenocortical axis) is activated, producing high concentrations of circulating adrenal glucocorticoids (GC) which, when chronically present, negatively influence an animal’s health and can lead to reproductive suppression in male [[marmot]]s (''Marmota marmota''), and blocks of ovulatory cycles of female talapoin monkeys (''Miopithecus talapoin''), meerkats (''Suricata suricatta'') and marmots.<ref name=ref14 /><ref name=ref22 /><ref name=ref23 /><ref name=ref24 />
Chronic physiological stress resulting from aggression by dominant toward subordinate individuals is thought to be a major cause of delayed maturation and suppressed ovulation in subordinate individuals of a wide range of species.<ref name=ref14 /><ref name=ref22>{{cite journal | last1 = Bowman | first1 = L. | last2 = Dilley | first2 = S.R. | last3 = Keverne | first3 = E.B. | year = 1978 | title = Supression of oestrogen-induced LH surges by social subordination in talapoin monkeys | url = | journal = Nature | volume = 275 | issue = | pages = 56–58 | doi=10.1038/275056a0}}</ref><ref name=ref23>Arnold, W. & Dittami, J. (1997) Reproductive suppression in male alpine marmots Animal Behaviour 53: 53–66.</ref><ref name=ref24>Hacklander, K., Mostl, E, Arnold, W. (2003) Reproductive suppression in female Alpine marmots (Marmota marmot) Animal Behavior 65: 1133-1140.</ref> In response to stress the HPA axis (hypothalamic-pituitary-adrenocortical axis) is activated, producing high concentrations of circulating adrenal glucocorticoids (GC) which, when chronically present, negatively influence an animal’s health and can lead to reproductive suppression in male [[marmot]]s (''Marmota marmota''), and blocks of ovulatory cycles of female talapoin monkeys (''Miopithecus talapoin''), meerkats (''Suricata suricatta'') and marmots.<ref name=ref14 /><ref name=ref22 /><ref name=ref23 /><ref name=ref24 />


In cooperatively breeding meerkats (Suricata suricatta) the dominant breeding female is the oldest and heaviest female who is highly aggressive toward subordinate females during the breeding season and temporarily evicts subordinate females from the group.<ref name=ref14 /> Evicted subordinates suffer repeated attacks during the later stages of the breeding female’s pregnancy and showed GC levels two times higher than normal. Approximately 3 days after their birth, subordinate females return to the group to help rear the breeding female’s pups, at which time the dominant female is no longer aggressive toward them. By inducing the stress response in subordinates the breeding female disrupts the ovulatory cycle and prevents mating of the subordinate females, or causes the pregnancies of subordinates to fail if they do occur. If her social group is small the breeding female evicts all subordinate females, but if it is large she targets older females, pregnant females and non-kin.<ref name=ref14 />
In cooperatively breeding meerkats (Suricata suricatta) the dominant breeding female is the oldest and heaviest female who is highly aggressive toward subordinate females during the breeding season and temporarily evicts subordinate females from the group.<ref name=ref14 /> Evicted subordinates suffer repeated attacks during the later stages of the breeding female’s pregnancy and showed GC levels two times higher than normal. Approximately 3 days after their birth, subordinate females return to the group to help rear the breeding female’s pups, at which time the dominant female is no longer aggressive toward them. By inducing the stress response in subordinates the breeding female disrupts the ovulatory cycle and prevents mating of the subordinate females, or causes the pregnancies of subordinates to fail if they do occur. If her social group is small the breeding female evicts all subordinate females, but if it is large she targets older females, pregnant females and non-kin.<ref name=ref14 />


However, reproductive suppression through stress does not apply to many species including orangutans for which subordinate males have lower GC levels than dominant ones,<ref name=ref25>Maggioncalda, A.N. & Sapolsky, R.M. (2002) Disturbing behaviors of the organutan. Scientific American June: 60-65.</ref> marmosets for which nonbreeding subordinate females were not found to have higher GC levels than dominant breeding females,<ref name=ref26>{{cite journal | last1 = Abbott | first1 = D.H. | last2 = Keverne | first2 = E.B. | last3 = Bercovitch | first3 = F.B. | last4 = Shively | first4 = C.A. | last5 = Mendoza | first5 = S.P. | last6 = Saltzman | first6 = W. | last7 = Snowdon | first7 = C.T. | last8 = Ziegler | first8 = T.E. | last9 = Banjevic | first9 = M. | last10 = Garland | first10 = T Jr. | last11 = Sapolsky | first11 = R.M. | year = 2003 | title = Are subordinates always stressed? A comparative analysis of rank differences in cortisol levels among primates | url = | journal = Hormones and Behavior | volume = 43 | issue = | pages = 67–82 }}</ref> social carnivores and other animals.<ref name=ref27>{{cite journal | last1 = Creel | first1 = S | year = 2005 | title = Dominance, aggression and glucocorticoid levels in social carnivores | url = | journal = Journal of Mammalogy | volume = 86 | issue = | pages = 255–264 }}</ref><ref name=ref28>{{cite journal | last1 = Hamilton | first1 = I.M. | year = 2004 | title = A commitment model of reproductive inhibition in cooperatively breeding groups | url = | journal = Behavioral Ecology | volume = 15 | issue = | pages = 585–591 }}</ref> Some argue that when a variety of variables are controlled for, reanalysis of the GC data for meerkats does not support a correlation between high GC levels and a subordinate position in the social hierarchy.<ref name=ref29>{{cite journal | last1 = Barrette | first1 = M-F | last2 = Monfort | first2 = S.L. | last3 = Festa-Bianche | first3 = M. | last4 = Clutton-Brock | first4 = T.H. | last5 = Russell | first5 = A.F. | year = 2012 | title = Reproductive rate, not dominance status, affects fecal glucocorticoid levels in breeding female meerkats | url = | journal = Hormones and Behavior | volume = 61 | issue = | pages = 463–471 }}</ref> Dominant breeding males and females are often found to have higher GC levels among the dwarf mongoose (''Helogale parvula''), African wild dogs (''Lycaon pictus'') and gray wolves (Canis lupus) in which older and heavier individuals make up the breeding individuals in the group with younger individuals suppressing their reproduction and instead helping to raise the pups of the older breeding individuals.<ref name=ref27 />
However, reproductive suppression through stress does not apply to many species including orangutans for which subordinate males have lower GC levels than dominant ones,<ref name=ref25>Maggioncalda, A.N. & Sapolsky, R.M. (2002) Disturbing behaviors of the organutan. Scientific American June: 60-65.</ref> marmosets for which nonbreeding subordinate females were not found to have higher GC levels than dominant breeding females,<ref name=ref26>{{cite journal | last1 = Abbott | first1 = D.H. | last2 = Keverne | first2 = E.B. | last3 = Bercovitch | first3 = F.B. | last4 = Shively | first4 = C.A. | last5 = Mendoza | first5 = S.P. | last6 = Saltzman | first6 = W. | last7 = Snowdon | first7 = C.T. | last8 = Ziegler | first8 = T.E. | last9 = Banjevic | first9 = M. | last10 = Garland | first10 = T Jr. | last11 = Sapolsky | first11 = R.M. | year = 2003 | title = Are subordinates always stressed? A comparative analysis of rank differences in cortisol levels among primates | url = | journal = Hormones and Behavior | volume = 43 | issue = | pages = 67–82 | doi=10.1016/s0018-506x(02)00037-5}}</ref> social carnivores and other animals.<ref name=ref27>{{cite journal | last1 = Creel | first1 = S | year = 2005 | title = Dominance, aggression and glucocorticoid levels in social carnivores | url = | journal = Journal of Mammalogy | volume = 86 | issue = | pages = 255–264 | doi=10.1644/bhe-002.1}}</ref><ref name=ref28>{{cite journal | last1 = Hamilton | first1 = I.M. | year = 2004 | title = A commitment model of reproductive inhibition in cooperatively breeding groups | url = | journal = Behavioral Ecology | volume = 15 | issue = | pages = 585–591 | doi=10.1093/beheco/arh047}}</ref> Some argue that when a variety of variables are controlled for, reanalysis of the GC data for meerkats does not support a correlation between high GC levels and a subordinate position in the social hierarchy.<ref name=ref29>{{cite journal | last1 = Barrette | first1 = M-F | last2 = Monfort | first2 = S.L. | last3 = Festa-Bianche | first3 = M. | last4 = Clutton-Brock | first4 = T.H. | last5 = Russell | first5 = A.F. | year = 2012 | title = Reproductive rate, not dominance status, affects fecal glucocorticoid levels in breeding female meerkats | url = | journal = Hormones and Behavior | volume = 61 | issue = | pages = 463–471 | doi=10.1016/j.yhbeh.2011.12.005}}</ref> Dominant breeding males and females are often found to have higher GC levels among the dwarf mongoose (''Helogale parvula''), African wild dogs (''Lycaon pictus'') and gray wolves (Canis lupus) in which older and heavier individuals make up the breeding individuals in the group with younger individuals suppressing their reproduction and instead helping to raise the pups of the older breeding individuals.<ref name=ref27 />


====Pheromonal suppression by breeding female====
====Pheromonal suppression by breeding female====
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Yellow, banded and dwarf mongooses live in families similar to wolf packs with scent marking done almost exclusively by the dominant pair. Dwarf mongooses show synchronous estrous but only the dominant female regularly gives birth. Subordinate females do not conceive or abort early, but do lactate after the dominant female gives birth and participate in communal nursing. When the subordinate females leave the parental pack they will become fully reproductively active in new groups they help establish. In captivity more than one dwarf mongoose in a group can give birth but the young of subordinates do not survive. However, if the size of their cage is increased and density is lower, reproductive activity of subordinates resumes. As in wolves, pheromonal control over the reproductive cycle of the mongoose is implicated as the mechanism for reproductive suppression.<ref name=ref8 />
Yellow, banded and dwarf mongooses live in families similar to wolf packs with scent marking done almost exclusively by the dominant pair. Dwarf mongooses show synchronous estrous but only the dominant female regularly gives birth. Subordinate females do not conceive or abort early, but do lactate after the dominant female gives birth and participate in communal nursing. When the subordinate females leave the parental pack they will become fully reproductively active in new groups they help establish. In captivity more than one dwarf mongoose in a group can give birth but the young of subordinates do not survive. However, if the size of their cage is increased and density is lower, reproductive activity of subordinates resumes. As in wolves, pheromonal control over the reproductive cycle of the mongoose is implicated as the mechanism for reproductive suppression.<ref name=ref8 />
The house mouse (''Mus musculus'') is territorial with a single dominant male marking its territorial boundary with urine while subordinate males do not urine mark.<ref name=ref30>{{cite journal | last1 = Bronson | first1 = F.H. | year = 1979 | title = The reproductive ecology of the house mouse | url = | journal = The Quarterly Review of Biology | volume = 54 | issue = | pages = 265–299 }}</ref> A female’s rate of urine marking is elevated in response to a dominant male’s urine marking, and his urine contains pheromones that accelerate her ovulation. The presence of a dominant adult male and his urine are crucial for young females to initiate puberty. Females isolated from males often do not experience puberty or have unstable ovulatory cycles. Contact with the urine of a dominant female signals a young prepubescent female to delay the onset of puberty. When housed with only an adult male, female mice reach puberty within 25 days, but puberty will not occur until 40–50 days if they are housed with adult females. Being grouped with other females suppresses the young female’s serum LH and prolactin. Exposure to the male elevates their LH levels followed by increased serum estradiol. Female mice have a short ovulatory cycle when housed with males and a long cycle when housed with only other females.<ref name=ref30 />
The house mouse (''Mus musculus'') is territorial with a single dominant male marking its territorial boundary with urine while subordinate males do not urine mark.<ref name=ref30>{{cite journal | last1 = Bronson | first1 = F.H. | year = 1979 | title = The reproductive ecology of the house mouse | url = | journal = The Quarterly Review of Biology | volume = 54 | issue = | pages = 265–299 | doi=10.1086/411295}}</ref> A female’s rate of urine marking is elevated in response to a dominant male’s urine marking, and his urine contains pheromones that accelerate her ovulation. The presence of a dominant adult male and his urine are crucial for young females to initiate puberty. Females isolated from males often do not experience puberty or have unstable ovulatory cycles. Contact with the urine of a dominant female signals a young prepubescent female to delay the onset of puberty. When housed with only an adult male, female mice reach puberty within 25 days, but puberty will not occur until 40–50 days if they are housed with adult females. Being grouped with other females suppresses the young female’s serum LH and prolactin. Exposure to the male elevates their LH levels followed by increased serum estradiol. Female mice have a short ovulatory cycle when housed with males and a long cycle when housed with only other females.<ref name=ref30 />


Queen pheromones are among the most important chemical messages regulating insect societies but are yet to be isolated.<ref name="ref31">Holman, L., Lanfear, R., d’Ettorre P. (2013) The evolution of queen pheromones in the ant genus Lasius. Journal of Evolutionary Biology 26” 1549–1558.</ref> in natural colonies of the Saxon wasp, Dolichovespula saxonica, queens emit reliable chemical cues of their true fertility, but as the queen’s signals decrease incidences of worker reproduction increases.<ref name="ref32">{{cite journal | last1 = Van Zweden | first1 = J.S. | last2 = Bonckaert | first2 = W. | last3 = Wenseleers | first3 = T. | last4 = d'Ettorre | first4 = P | year = 2013 | title = Queen signaling in social wasps | url = | journal = Evolution | volume = 68 | issue = | pages = 976–986 }}</ref> In colonies of ''[[Bombus terrestris]]'', the queen can control oogenesis and worker egg laying by regulating concentrations of juvenile hormone (JH) in workers. This is likely achieved through queen pheromones. <ref>{{cite journal | author = Roseler, P. F. | year= 1977 | title = Juvenile hormone control of oogenesis in bumblebee workers, ''B. terrestris'' | journal = Journal of Insect Physiology | volume = 23 | pages = 985–992 | doi=10.1016/0022-1910(77)90126-3}}</ref>
Queen pheromones are among the most important chemical messages regulating insect societies but are yet to be isolated.<ref name="ref31">Holman, L., Lanfear, R., d’Ettorre P. (2013) The evolution of queen pheromones in the ant genus Lasius. Journal of Evolutionary Biology 26” 1549–1558.</ref> in natural colonies of the Saxon wasp, Dolichovespula saxonica, queens emit reliable chemical cues of their true fertility, but as the queen’s signals decrease incidences of worker reproduction increases.<ref name="ref32">{{cite journal | last1 = Van Zweden | first1 = J.S. | last2 = Bonckaert | first2 = W. | last3 = Wenseleers | first3 = T. | last4 = d'Ettorre | first4 = P | year = 2013 | title = Queen signaling in social wasps | url = | journal = Evolution | volume = 68 | issue = | pages = 976–986 | doi=10.1111/evo.12314}}</ref> In colonies of ''[[Bombus terrestris]]'', the queen can control oogenesis and worker egg laying by regulating concentrations of juvenile hormone (JH) in workers. This is likely achieved through queen pheromones. <ref>{{cite journal | author = Roseler, P. F. | year= 1977 | title = Juvenile hormone control of oogenesis in bumblebee workers, ''B. terrestris'' | journal = Journal of Insect Physiology | volume = 23 | pages = 985–992 | doi=10.1016/0022-1910(77)90126-3}}</ref>


====Social Self-inhibition hypothesis====
====Social Self-inhibition hypothesis====
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===Mate guarding===
===Mate guarding===
[[File:Yellow mongoose 1.jpg|thumb|Yellow mongoose 1]]
[[File:Yellow mongoose 1.jpg|thumb|Yellow mongoose 1]]
Limiting access to reproductive partners through mate guarding is a form of reproductive suppression. In the banded mongoose (Mungus mungo) the oldest males have the most offspring. Yet mating in this species is highly promiscuous.<ref name=ref34>{{cite journal | last1 = Nichols | first1 = H.J. | last2 = Amos | first2 = W. | last3 = Cant | first3 = M.A. | last4 = Bell | first4 = M.B.V. | last5 = Hodge | first5 = S.J. | year = 2010 | title = Top males gain high reproductive success by guarding more successful females in a cooperatively breeding mongoose | url = | journal = Animal Behaviour | volume = 80 | issue = | pages = 649–657 }}</ref> The older males increase their reproductive success by mate guarding the oldest most fertile females since they cannot guard all the females in the group.<ref name=ref34 /> Therefore, successfully breeding older males are highly selective in their mate guarding and exert mate selection. Mate guarding is also a mechanism of reproductive suppression of subordinates in mandrills (Mandrillus sphinx) in which males over the age of 8 mate-guard, with alpha males performing 94% of the mate-guarding and being responsible for siring 69% of the offspring.<ref name=ref35>{{cite journal | last1 = Setchell | first1 = J.M. | last2 = Charpentier | first2 = M. | last3 = Wickings | first3 = J. | year = 2005 | title = Mate guarding and paternity in mandrills: factors influencing alpha male monopoly | url = | journal = Animal Behaviour | volume = 70 | issue = | pages = 1105–1120 }}</ref>
Limiting access to reproductive partners through mate guarding is a form of reproductive suppression. In the banded mongoose (Mungus mungo) the oldest males have the most offspring. Yet mating in this species is highly promiscuous.<ref name=ref34>{{cite journal | last1 = Nichols | first1 = H.J. | last2 = Amos | first2 = W. | last3 = Cant | first3 = M.A. | last4 = Bell | first4 = M.B.V. | last5 = Hodge | first5 = S.J. | year = 2010 | title = Top males gain high reproductive success by guarding more successful females in a cooperatively breeding mongoose | url = | journal = Animal Behaviour | volume = 80 | issue = | pages = 649–657 | doi=10.1016/j.anbehav.2010.06.025}}</ref> The older males increase their reproductive success by mate guarding the oldest most fertile females since they cannot guard all the females in the group.<ref name=ref34 /> Therefore, successfully breeding older males are highly selective in their mate guarding and exert mate selection. Mate guarding is also a mechanism of reproductive suppression of subordinates in mandrills (Mandrillus sphinx) in which males over the age of 8 mate-guard, with alpha males performing 94% of the mate-guarding and being responsible for siring 69% of the offspring.<ref name=ref35>{{cite journal | last1 = Setchell | first1 = J.M. | last2 = Charpentier | first2 = M. | last3 = Wickings | first3 = J. | year = 2005 | title = Mate guarding and paternity in mandrills: factors influencing alpha male monopoly | url = | journal = Animal Behaviour | volume = 70 | issue = | pages = 1105–1120 | doi=10.1016/j.anbehav.2005.02.021}}</ref>


===Genetic determinism of reproductive despotism - eusocial insects and the naked mole rat with suppression at birth===
===Genetic determinism of reproductive despotism - eusocial insects and the naked mole rat with suppression at birth===
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===Destruction of eggs including worker policing===
===Destruction of eggs including worker policing===
Destroying eggs such that only one female’s eggs survive is documented in cooperatively breeding birds such as acorn woodpeckers (''Melanerpes formicivorus'').<ref name=ref7 /> About 25% of acorn woodpecker groups contain two or more joint-nesting females that cooperate to raise young, but cooperative female destroy each other’s eggs prior to laying their own. These eggs are eaten by other members of the group, including the mother.
Destroying eggs such that only one female’s eggs survive is documented in cooperatively breeding birds such as acorn woodpeckers (''Melanerpes formicivorus'').<ref name=ref7 /> About 25% of acorn woodpecker groups contain two or more joint-nesting females that cooperate to raise young, but cooperative female destroy each other’s eggs prior to laying their own. These eggs are eaten by other members of the group, including the mother.
In Cape honeybees (''Apis mellifera capensis'') the multiple mating of the queen and existence of half-siblings creates sub-families within the colony. Sometimes the queen fails to control worker reproduction. In response workers remove eggs laid by other workers leading to less than 1% of offspring being worker laid.<ref name=ref5 /> Worker Policing of worker eggs occurs in the European hornet (Vespa crabo) honeybees and wasps.<ref name=ref36>{{cite journal | last1 = Foster | first1 = K.R. | last2 = Gulliver | first2 = J. | last3 = Ratneiks | first3 = F.L.W. | year = 2002 | title = Worker policing in the European hornet Vespa crabro | url = | journal = Insectes soc. | volume = 49 | issue = | pages = 41–44 }}</ref><ref name=ref37>{{cite journal | last1 = Foster | first1 = K.R. | last2 = Ratnieks | first2 = F.L.W. | year = 2001 | title = Convergent evolution of worker policing by egg eating in the honeybee and common wasp | url = | journal = Proceedings of the Royal Society Biological Sciences | volume = 268 | issue = | pages = 169–174 }}</ref>
In Cape honeybees (''Apis mellifera capensis'') the multiple mating of the queen and existence of half-siblings creates sub-families within the colony. Sometimes the queen fails to control worker reproduction. In response workers remove eggs laid by other workers leading to less than 1% of offspring being worker laid.<ref name=ref5 /> Worker Policing of worker eggs occurs in the European hornet (Vespa crabo) honeybees and wasps.<ref name=ref36>{{cite journal | last1 = Foster | first1 = K.R. | last2 = Gulliver | first2 = J. | last3 = Ratneiks | first3 = F.L.W. | year = 2002 | title = Worker policing in the European hornet Vespa crabro | url = | journal = Insectes soc. | volume = 49 | issue = | pages = 41–44 | doi=10.1007/s00040-002-8277-z}}</ref><ref name=ref37>{{cite journal | last1 = Foster | first1 = K.R. | last2 = Ratnieks | first2 = F.L.W. | year = 2001 | title = Convergent evolution of worker policing by egg eating in the honeybee and common wasp | url = | journal = Proceedings of the Royal Society Biological Sciences | volume = 268 | issue = | pages = 169–174 | doi=10.1098/rspb.2000.1346}}</ref>


===Spontaneous abortion===
===Spontaneous abortion===
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===Brood parasitism and quasi-parasitism in birds===
===Brood parasitism and quasi-parasitism in birds===
[[File:Senegal Coucal -Centropus senegalensis -on tree.jpg|thumb|Senegal Coucal - ''Centropus senegalensis'' - on tree]]
[[File:Senegal Coucal -Centropus senegalensis -on tree.jpg|thumb|Senegal Coucal - ''Centropus senegalensis'' - on tree]]
[[Brood parasite|Brood parasitism]] is the process by which a female lays her eggs in a conspecific female’s nest. Parasitic female moorhens (Gallinula chloropus) are known to lay one to six eggs in their neighbor’s nests.<ref name=ref40>{{cite journal | last1 = McRae | first1 = S. B. | last2 = Burke | first2 = T. | year = 1996 | title = Intraspecific brood parasitism in the moorhen: parentage and parasite-host relationships determined by DNA fingerprinting | url = | journal = Behavioral Ecology and Sociobiology | volume = 38 | issue = 2| pages = 115–129 }}</ref> In most cases the male paired with the conspecific female has been involved in extra-pair copulations with the parasitic mother. This causes maternity uncertainty for the female as not all species can readily identify their own eggs from another’s, which imposes fitness costs of raising an offspring that is not her own. In some cases females will lay eggs in another’s nest that were conceived by another male entirely. This process is known as quasi-parasitism and induces fitness costs on both the male and female of the parasitized nest who cannot be certain of paternity or maternity. This is a problem for white-fronted bee-eaters (Merops bullockoides), where it has been found through analysis of enzyme polymorphisms that approximately 9–12% of offspring are unrelated to one parent or none.<ref name=ref41>{{cite journal | last1 = Wrege | first1 = P. H. | last2 = Emlen | first2 = S. T. | year = 1987 | title = Biochemical determination of parental uncertainty in white-fronted bee-eaters | url = | journal = Behavioral Ecology and Sociobiology | volume = 20 | issue = 3| pages = 153–160 }}</ref> The reproductive strategy of brood-parasitism is not only an intraspecies problem, as parasitic mothers will use the nests of one to 240 different host species.<ref name=ref42>Lanyon, S. M. (1992). Interspecific brood parasitism in blackbirds (''Icterinae''): A phylogenetic perspective. Science(Washington), 255(5040), 77–79.</ref> The fitness costs that these interactions impose strains on host parents to displace time, effort, and resources into offspring that are not their own, and are believed to reduce the hosts reproductive success by up to 50%.<ref name=ref43>{{cite journal | last1 = Langmore | first1 = N. E. | last2 = Hunt | first2 = S. | last3 = Kilner | first3 = R. M. | year = 2003 | title = Escalation of a coevolutionary arms race through host rejection of brood parasitic young | url = | journal = Nature | volume = 422 | issue = 6928| pages = 157–160 }}</ref> But time lost is not the greatest cost to some host species. Hosts that raise Cuculus and Chrysococcyx cuckoos lose all their offspring as the cuckoos kill them with mandibular hooks.<ref name=ref44>{{cite journal | last1 = Davies | first1 = N. B. | last2 = Bourke | first2 = A. F. | last3 = de L Brooke | first3 = M. | year = 1989 | title = Cuckoos and parasitic ants: interspecific brood parasitism as an evolutionary arms race | url = | journal = Trends in Ecology & Evolution | volume = 4 | issue = 9| pages = 274–278 }}</ref> While some other species do not directly kill a hosts’ young, they often kill them indirectly through competition for food leading to eventual starvation.<ref name=ref44 />
[[Brood parasite|Brood parasitism]] is the process by which a female lays her eggs in a conspecific female’s nest. Parasitic female moorhens (Gallinula chloropus) are known to lay one to six eggs in their neighbor’s nests.<ref name=ref40>{{cite journal | last1 = McRae | first1 = S. B. | last2 = Burke | first2 = T. | year = 1996 | title = Intraspecific brood parasitism in the moorhen: parentage and parasite-host relationships determined by DNA fingerprinting | url = | journal = Behavioral Ecology and Sociobiology | volume = 38 | issue = 2| pages = 115–129 | doi=10.1007/s002650050224}}</ref> In most cases the male paired with the conspecific female has been involved in extra-pair copulations with the parasitic mother. This causes maternity uncertainty for the female as not all species can readily identify their own eggs from another’s, which imposes fitness costs of raising an offspring that is not her own. In some cases females will lay eggs in another’s nest that were conceived by another male entirely. This process is known as quasi-parasitism and induces fitness costs on both the male and female of the parasitized nest who cannot be certain of paternity or maternity. This is a problem for white-fronted bee-eaters (Merops bullockoides), where it has been found through analysis of enzyme polymorphisms that approximately 9–12% of offspring are unrelated to one parent or none.<ref name=ref41>{{cite journal | last1 = Wrege | first1 = P. H. | last2 = Emlen | first2 = S. T. | year = 1987 | title = Biochemical determination of parental uncertainty in white-fronted bee-eaters | url = | journal = Behavioral Ecology and Sociobiology | volume = 20 | issue = 3| pages = 153–160 | doi=10.1007/bf00299728}}</ref> The reproductive strategy of brood-parasitism is not only an intraspecies problem, as parasitic mothers will use the nests of one to 240 different host species.<ref name=ref42>Lanyon, S. M. (1992). Interspecific brood parasitism in blackbirds (''Icterinae''): A phylogenetic perspective. Science(Washington), 255(5040), 77–79.</ref> The fitness costs that these interactions impose strains on host parents to displace time, effort, and resources into offspring that are not their own, and are believed to reduce the hosts reproductive success by up to 50%.<ref name=ref43>{{cite journal | last1 = Langmore | first1 = N. E. | last2 = Hunt | first2 = S. | last3 = Kilner | first3 = R. M. | year = 2003 | title = Escalation of a coevolutionary arms race through host rejection of brood parasitic young | url = | journal = Nature | volume = 422 | issue = 6928| pages = 157–160 | doi=10.1038/nature01460}}</ref> But time lost is not the greatest cost to some host species. Hosts that raise Cuculus and Chrysococcyx cuckoos lose all their offspring as the cuckoos kill them with mandibular hooks.<ref name=ref44>{{cite journal | last1 = Davies | first1 = N. B. | last2 = Bourke | first2 = A. F. | last3 = de L Brooke | first3 = M. | year = 1989 | title = Cuckoos and parasitic ants: interspecific brood parasitism as an evolutionary arms race | url = | journal = Trends in Ecology & Evolution | volume = 4 | issue = 9| pages = 274–278 | doi=10.1016/0169-5347(89)90202-4}}</ref> While some other species do not directly kill a hosts’ young, they often kill them indirectly through competition for food leading to eventual starvation.<ref name=ref44 />
Why then do host species tolerate parasitic offspring? Several hypotheses have been tested to answer this question. One theory known as the quasi-parasitism hypothesis suggested that parasitic females were exchanging extra-pair copulations with host males for access to lay their eggs in the nest. This theory was denounced by DNA fingerprinting revealing that many offspring were sired by only the parasitic mother’s mate and not the mate of the host female.<ref name=ref40 /> Another theory was that this interaction fell under kin selection, and that perhaps the parasites and hosts were closely related and there was an inclusive fitness benefit to hosts. While this theory has not been completely denounced in some species like moorhens, it does not fully explain why then interspecific parasitism perseveres.<ref name=ref40 /> The most widely accepted hypothesis is that hosts are deceived and cannot differentiate their own eggs or offspring. The deception model explains a coevolutionary arms race between hosts and parasites that has led to further adaptations in deception and host parasitism defense strategies. Parasitic cuckoos have developed a system for potentially successful parasitism by quickly laying a small mimetic egg during the hosts’ laying period.<ref name=ref44 /> Some parasitic mothers go as far to eject the eggs of hosts before laying their own eggs in the nest, which has been suggested to increase the efficiency of which their eggs are incubated and raised, all the while providing them with a meal in the process.<ref name=ref44 /> Brood parasitism has been shown to be a coevolutionary arms race between hosts and parasites with new adaptations of egg recognition being selected for in hosts, and new strategies of trickery and deception being selected for in parasites to exploit hosts.<ref name=ref43 />
Why then do host species tolerate parasitic offspring? Several hypotheses have been tested to answer this question. One theory known as the quasi-parasitism hypothesis suggested that parasitic females were exchanging extra-pair copulations with host males for access to lay their eggs in the nest. This theory was denounced by DNA fingerprinting revealing that many offspring were sired by only the parasitic mother’s mate and not the mate of the host female.<ref name=ref40 /> Another theory was that this interaction fell under kin selection, and that perhaps the parasites and hosts were closely related and there was an inclusive fitness benefit to hosts. While this theory has not been completely denounced in some species like moorhens, it does not fully explain why then interspecific parasitism perseveres.<ref name=ref40 /> The most widely accepted hypothesis is that hosts are deceived and cannot differentiate their own eggs or offspring. The deception model explains a coevolutionary arms race between hosts and parasites that has led to further adaptations in deception and host parasitism defense strategies. Parasitic cuckoos have developed a system for potentially successful parasitism by quickly laying a small mimetic egg during the hosts’ laying period.<ref name=ref44 /> Some parasitic mothers go as far to eject the eggs of hosts before laying their own eggs in the nest, which has been suggested to increase the efficiency of which their eggs are incubated and raised, all the while providing them with a meal in the process.<ref name=ref44 /> Brood parasitism has been shown to be a coevolutionary arms race between hosts and parasites with new adaptations of egg recognition being selected for in hosts, and new strategies of trickery and deception being selected for in parasites to exploit hosts.<ref name=ref43 />



Revision as of 09:48, 4 August 2016

White-headed marmoset

Reproductive Suppression involves the prevention or inhibition of reproduction in otherwise healthy adult individuals.[1] It includes delayed sexual maturation (puberty) or inhibition of sexual receptivity, facultatively increased interbirth interval through delayed or inhibited ovulation or spontaneous or induced abortion, abandonment of immature and dependent offspring, mate guarding, selective destruction and worker policing of eggs in some eusocial insects or cooperatively breeding birds, and infanticide (see also infanticide (zoology)), and infanticide in carnivores) of the offspring of subordinate females either by directly killing by dominant females or males in mammals or indirectly through the withholding of assistance with infant care in marmosets and some carnivores.[2][3] The Reproductive Suppression Model argues that “females can optimize their lifetime reproductive success by suppressing reproduction when future [physical or social] conditions for the survival of offspring are likely to be greatly improved over present ones”.[1] When intragroup competition (competition between individuals belonging to the same group) is high it may be beneficial to suppress the reproduction of others, and for subordinate females to suppress their own reproduction until a later time when social competition is reduced. This leads to reproductive skew within a social group, with some individuals having more offspring than others. The cost of reproductive suppression to the individual is lowest at the earliest stages of a reproductive event and reproductive suppression is often easiest to induce at the pre-ovulatory or earliest stages of pregnancy in mammals, and greatest after a birth. Therefore, neuroendocrine cues for assessing reproductive success should evolve to be reliable at early stages in the ovulatory cycle. Reproductive suppression occurs in its most extreme form in eusocial insects such as termites, hornets and bees and the mammalian naked mole rat which depend on a complex division of labor within the group for survival and in which specific genes, epigenetics and other factors are known to determine whether individuals will permanently be unable to breed or able to reach reproductive maturity under particular social conditions,[4][5][6] and cooperatively breeding fish, birds and mammals in which a breeding pair depends on helpers whose reproduction is suppressed for the survival of their own offspring.[7][8][9][10][11][12][13][14][15][16] In eusocial and cooperatively breeding animals most non-reproducing helpers engage in kin selection, enhancing their own inclusive fitness by ensuring the survival of offspring they are closely related to.[17] Wolf packs suppress subordinate breeding.

Pre-fertilization mechanisms of reproductive suppression

Environmental Cues

Food Shortages (resource availability)

Female mammals experience delays in the onset of puberty or increase their interbirth intervals in response to environmental conditions that are associated with low abundance and poor quality of foods. Nutritional stress is apparently linked to the female endocrine system and ovulatory pheromonal cycle. For example, Orangutans (Pongo pygmaeus) experience high ketone (due to fat burning) and low estrogen levels during times of low food availability and poor food quality, but low ketone and high estrogen levels that stimulates onset of the ovulation during the fruit masting seasons that occurs about every four years on Sumatra.[18][18] Since adult female orangutans are solitary, interference by other females can be ruled out as influencing their temporary reproductive suppression and facultatively long interbirth intervals. Polygynandrous yellow baboons (Papio cynocephalus) in Kenya were far less likely to ovulate or conceive during periods of drought or extreme heat, especially if they live in large groups, resulting in longer interbirth intervals during periods of nutritional and thermal stress.[19][20]

High population density

High population density is one of the environmental factors that can lead to reproductive suppression. When population density is high, subordinate individuals may experience reproductive suppression that they would not have experiences otherwise. For example, when high numbers of yellow baboon (Papio cynocephalus) females are simultaneously in estrous at Mikumi National Park, Tanzania dominant females form coalitions that attack subordinate females, leading to a disruption in their reproductive cycle and failure to conceive.[1] This places constraints on the number of offspring born in a single generation. Since infant mortality in Amboseli yellow baboons depends in part on the number and ages of other infants born into the group, pre-ovulatory females that are most susceptible to stress-induced delay or inhibition of ovulation are the most frequent targets of female coalition attacks. Female attackers are often in advanced stages of pregnancy, and have the most to lose if the number of infants in the group reaches an unsustainable level. A similar study of Chacma baboons (Papio ursinus) noted high levels of female-female aggression around the mating season when the number of ovulating females was high (indicated by sexual swellings) and that aggression directed toward suppressing the mating opportunities of ovulating females.[21] Among elephant seals (Mirounga) high neonatal mortality occurs when the number of pups born in a season is high, with deaths resulting from injury and starvation.[1] To counteract loss of their pups elephant seals conceive next year’s offspring immediately after giving birth to this year’s young, but delay implantation for 4 months. Female striped mice (Rhabdomys pumilio) in monogamous social groups do not experience reproductive suppression, but those living in communally breeding groups with high population density and large numbers of old breeding females do.[16]

Social Cues

Stress induced by aggression from dominant to subordinate individuals

Chronic physiological stress resulting from aggression by dominant toward subordinate individuals is thought to be a major cause of delayed maturation and suppressed ovulation in subordinate individuals of a wide range of species.[14][22][23][24] In response to stress the HPA axis (hypothalamic-pituitary-adrenocortical axis) is activated, producing high concentrations of circulating adrenal glucocorticoids (GC) which, when chronically present, negatively influence an animal’s health and can lead to reproductive suppression in male marmots (Marmota marmota), and blocks of ovulatory cycles of female talapoin monkeys (Miopithecus talapoin), meerkats (Suricata suricatta) and marmots.[14][22][23][24]

In cooperatively breeding meerkats (Suricata suricatta) the dominant breeding female is the oldest and heaviest female who is highly aggressive toward subordinate females during the breeding season and temporarily evicts subordinate females from the group.[14] Evicted subordinates suffer repeated attacks during the later stages of the breeding female’s pregnancy and showed GC levels two times higher than normal. Approximately 3 days after their birth, subordinate females return to the group to help rear the breeding female’s pups, at which time the dominant female is no longer aggressive toward them. By inducing the stress response in subordinates the breeding female disrupts the ovulatory cycle and prevents mating of the subordinate females, or causes the pregnancies of subordinates to fail if they do occur. If her social group is small the breeding female evicts all subordinate females, but if it is large she targets older females, pregnant females and non-kin.[14]

However, reproductive suppression through stress does not apply to many species including orangutans for which subordinate males have lower GC levels than dominant ones,[25] marmosets for which nonbreeding subordinate females were not found to have higher GC levels than dominant breeding females,[26] social carnivores and other animals.[27][28] Some argue that when a variety of variables are controlled for, reanalysis of the GC data for meerkats does not support a correlation between high GC levels and a subordinate position in the social hierarchy.[29] Dominant breeding males and females are often found to have higher GC levels among the dwarf mongoose (Helogale parvula), African wild dogs (Lycaon pictus) and gray wolves (Canis lupus) in which older and heavier individuals make up the breeding individuals in the group with younger individuals suppressing their reproduction and instead helping to raise the pups of the older breeding individuals.[27]

Pheromonal suppression by breeding female

Pheromonal suppression of subordinate male and female reproduction is implicated as the mechanism by which dominant breeding pairs suppress the reproduction of non-breeders in communally and cooperatively breeding species, especially in the absence of stress as an explanation.[8] Wolves (Canis lupus), coyotes (Canis latrons) and hunting dogs (Lycaon pictus) live in packs with a dominant breeding pair that does most of the territorial urine scent marking in the group. During the breeding season the dominant male urinates over the dominant female’s urine, possibly to hide the female’s reproductive status from other males. Pheromones in urine are implicated as a possible mechanism to shut down the subordinate’s reproductive cycle. Only the dominant pair mate and have young, producing one litter per year. Subordinate females either do not exhibit estrous hormonal changes or they occur irregularly. Occasionally a subordinate animal leaves the pack and forms a new mating pair when it then exhibits of the territorial urine marking and mating behavior that was suppressed when living in the presence of the dominant breeding pair.[8]

Yellow, banded and dwarf mongooses live in families similar to wolf packs with scent marking done almost exclusively by the dominant pair. Dwarf mongooses show synchronous estrous but only the dominant female regularly gives birth. Subordinate females do not conceive or abort early, but do lactate after the dominant female gives birth and participate in communal nursing. When the subordinate females leave the parental pack they will become fully reproductively active in new groups they help establish. In captivity more than one dwarf mongoose in a group can give birth but the young of subordinates do not survive. However, if the size of their cage is increased and density is lower, reproductive activity of subordinates resumes. As in wolves, pheromonal control over the reproductive cycle of the mongoose is implicated as the mechanism for reproductive suppression.[8] The house mouse (Mus musculus) is territorial with a single dominant male marking its territorial boundary with urine while subordinate males do not urine mark.[30] A female’s rate of urine marking is elevated in response to a dominant male’s urine marking, and his urine contains pheromones that accelerate her ovulation. The presence of a dominant adult male and his urine are crucial for young females to initiate puberty. Females isolated from males often do not experience puberty or have unstable ovulatory cycles. Contact with the urine of a dominant female signals a young prepubescent female to delay the onset of puberty. When housed with only an adult male, female mice reach puberty within 25 days, but puberty will not occur until 40–50 days if they are housed with adult females. Being grouped with other females suppresses the young female’s serum LH and prolactin. Exposure to the male elevates their LH levels followed by increased serum estradiol. Female mice have a short ovulatory cycle when housed with males and a long cycle when housed with only other females.[30]

Queen pheromones are among the most important chemical messages regulating insect societies but are yet to be isolated.[31] in natural colonies of the Saxon wasp, Dolichovespula saxonica, queens emit reliable chemical cues of their true fertility, but as the queen’s signals decrease incidences of worker reproduction increases.[32] In colonies of Bombus terrestris, the queen can control oogenesis and worker egg laying by regulating concentrations of juvenile hormone (JH) in workers. This is likely achieved through queen pheromones. [33]

Social Self-inhibition hypothesis

Game theory is employed to suggest that subordinates suppress their own reproduction to avoid the social cost imposed on them if they reproduce, including expulsion from the group and infanticide against their progeny by dominant breeding individuals.[28] Forced dispersal from the group may be extremely dangerous, involving high levels of predation and difficulty finding food and sleeping sites. In the absence of stress or pheromones as a mechanism, a “self-inhibition”model was proposed that suggests subordinates can choose to inhibit their own reproduction in cooperatively breeding groups in order to remain flexible and share in the group’s productivity. When group members are closely related, independent breeding opportunities are poor, and detection of mating and pregnancy is high, subordinates choose to suppress their own reproduction.[28] The self-inhibition model has been applied to female common marmosets (Callithrix jacchus). When they are introduced into a new group, female marmosets are immediately subordinate, experience a drop in chrorionic gonadotrophin (CG) and within the first four days and stops ovulating.[3][34] Subordinate female ovaries are smaller than dominants and secrete little estrogen.[34] Older female marmosets are less subject to ovulatory self-restraint and the scent of an unfamiliar dominant female does not affect their ovulation. However, continued exposure to the dominant female may represent a social, rather than biological, cue that causes the subordinates to shut down their ovulation.[34]

Mate guarding

Yellow mongoose 1

Limiting access to reproductive partners through mate guarding is a form of reproductive suppression. In the banded mongoose (Mungus mungo) the oldest males have the most offspring. Yet mating in this species is highly promiscuous.[35] The older males increase their reproductive success by mate guarding the oldest most fertile females since they cannot guard all the females in the group.[35] Therefore, successfully breeding older males are highly selective in their mate guarding and exert mate selection. Mate guarding is also a mechanism of reproductive suppression of subordinates in mandrills (Mandrillus sphinx) in which males over the age of 8 mate-guard, with alpha males performing 94% of the mate-guarding and being responsible for siring 69% of the offspring.[36]

Genetic determinism of reproductive despotism - eusocial insects and the naked mole rat with suppression at birth

Also known as eusocialityOvary activation in honeybee workers is inhibited by pheromones from the queen.[5] In the Cape honeybee social parasites that are of the worker caste enter the colony and kill the resident queen, activate their own ovaries and parthenogenetically produce diploid female offspring (thelytoky) – behaviors that are all linked to a single locus on chromosome 13. The parasites produced queen-like pheromones falsely signally the presence of a queen suppressing the reproduction of worker’s native to the colony and policing or destroying these eggs.[5] Alternative slicing of a gene homologous to the gemini transcription factor of Drosophila controls worker sterility. Knocking out an exon resulted in rapid worker ovary activation. A 9 nucleotide deletion from the normal altruistic worker genome may turn a honeybee into a parasite.[5] As for many eusocial insects, termite workers are totipotent and rarely produce offspring although they are capable of reproduction when the breeding pair dies. Researchers hypothesized that the gene Neofem2, which is involved in cockroach communication, plays a critical role in queen-worker communication. They experimentally took the king or queen out of the colony. Some workers displayed pre-mating head butting behavior and can go on to become reproductive while others did not. However, when the Neofem2 gene was suppressed butting behavior did not occur, indicating that the gene is essential in allowing the queen to suppress worker reproduction.[4] Neofem2 may play a role in cockroach egg pheromones.[4] Naked mole rats resemble eusocial insects in becoming reversible nonbreeders at birth,.[1][6][37] Underground dwelling mole rats having an elaborate division of labor, high densities as colonies mature, high levels of inbreeding and extreme permanent reproductive despotism. Helping to rear the dominant females young may be the only way they can ensure an individual’s survival.

Post-fertilization mechanisms

Destruction of eggs including worker policing

Destroying eggs such that only one female’s eggs survive is documented in cooperatively breeding birds such as acorn woodpeckers (Melanerpes formicivorus).[7] About 25% of acorn woodpecker groups contain two or more joint-nesting females that cooperate to raise young, but cooperative female destroy each other’s eggs prior to laying their own. These eggs are eaten by other members of the group, including the mother. In Cape honeybees (Apis mellifera capensis) the multiple mating of the queen and existence of half-siblings creates sub-families within the colony. Sometimes the queen fails to control worker reproduction. In response workers remove eggs laid by other workers leading to less than 1% of offspring being worker laid.[5] Worker Policing of worker eggs occurs in the European hornet (Vespa crabo) honeybees and wasps.[38][39]

Spontaneous abortion

Social stress and resource limitation can lead to high rates of spontaneous abortion as a mechanism of reproductive suppression. Meerkats subordinate females that have conceived prior to being evicted from the group by the breeding female during the breeding season fail to carry their pregnancies as a result of increased stress (higher GClevels) and reduced access to food and other resources.[12][14] Evicted females regularly copulate with males from neighboring groups Subordinate females have low conception rates and increased abortion rates in response to low food availability and high predation risk.[14] Dwarf mongooses show synchronous estrous but only the dominant female regularly bears young. If subordinate females do manage to conceive they abort the pregnancy.[8]

Infanticide in cooperatively breeding species of subordinate offspring by the breeding female

Infanticide is a mechanism of reproductive success that occurs in many species. Alpha female dwarf mongooses and African wild dogs kill offpring other than their own, but alpha males do not use infanticide to enforce reproductive suppression.[27] This may occur because the breeding alpha may have sired a rare subordinate’s offspring. Subordinate females time their rare pregnancies such that they give birth several days after the alpha female to reduce the risk of infanticide. Pregnant suborordinate meerkats are known to kill the pups of the dominant breeding female.[14] No dominant female pups have ever been observed killed after their 4th day of life. Evicted subordinate females are kept out for 3 days after the breeding female gave birth. Eight infanticides involving the killing of a subordinate female’s offspring by the breeding female have been observed in wild common marmosets, as well as two instances of infanticide in which the subordinate female bred and then killed the breeding female’s babies.[3] Infanticidal marmoset females are often in the last trimester of pregnancy, but postpartum females don’t commit infanticide.

Brood parasitism and quasi-parasitism in birds

Senegal Coucal - Centropus senegalensis - on tree

Brood parasitism is the process by which a female lays her eggs in a conspecific female’s nest. Parasitic female moorhens (Gallinula chloropus) are known to lay one to six eggs in their neighbor’s nests.[40] In most cases the male paired with the conspecific female has been involved in extra-pair copulations with the parasitic mother. This causes maternity uncertainty for the female as not all species can readily identify their own eggs from another’s, which imposes fitness costs of raising an offspring that is not her own. In some cases females will lay eggs in another’s nest that were conceived by another male entirely. This process is known as quasi-parasitism and induces fitness costs on both the male and female of the parasitized nest who cannot be certain of paternity or maternity. This is a problem for white-fronted bee-eaters (Merops bullockoides), where it has been found through analysis of enzyme polymorphisms that approximately 9–12% of offspring are unrelated to one parent or none.[41] The reproductive strategy of brood-parasitism is not only an intraspecies problem, as parasitic mothers will use the nests of one to 240 different host species.[42] The fitness costs that these interactions impose strains on host parents to displace time, effort, and resources into offspring that are not their own, and are believed to reduce the hosts reproductive success by up to 50%.[43] But time lost is not the greatest cost to some host species. Hosts that raise Cuculus and Chrysococcyx cuckoos lose all their offspring as the cuckoos kill them with mandibular hooks.[44] While some other species do not directly kill a hosts’ young, they often kill them indirectly through competition for food leading to eventual starvation.[44] Why then do host species tolerate parasitic offspring? Several hypotheses have been tested to answer this question. One theory known as the quasi-parasitism hypothesis suggested that parasitic females were exchanging extra-pair copulations with host males for access to lay their eggs in the nest. This theory was denounced by DNA fingerprinting revealing that many offspring were sired by only the parasitic mother’s mate and not the mate of the host female.[40] Another theory was that this interaction fell under kin selection, and that perhaps the parasites and hosts were closely related and there was an inclusive fitness benefit to hosts. While this theory has not been completely denounced in some species like moorhens, it does not fully explain why then interspecific parasitism perseveres.[40] The most widely accepted hypothesis is that hosts are deceived and cannot differentiate their own eggs or offspring. The deception model explains a coevolutionary arms race between hosts and parasites that has led to further adaptations in deception and host parasitism defense strategies. Parasitic cuckoos have developed a system for potentially successful parasitism by quickly laying a small mimetic egg during the hosts’ laying period.[44] Some parasitic mothers go as far to eject the eggs of hosts before laying their own eggs in the nest, which has been suggested to increase the efficiency of which their eggs are incubated and raised, all the while providing them with a meal in the process.[44] Brood parasitism has been shown to be a coevolutionary arms race between hosts and parasites with new adaptations of egg recognition being selected for in hosts, and new strategies of trickery and deception being selected for in parasites to exploit hosts.[43]

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