Ecological and evolutionary preconditions of extended longevity in subterranean rodents
Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species...
Ausführliche Beschreibung
Autor*in: |
Novikov, E. A. [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2013 |
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Schlagwörter: |
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Anmerkung: |
© Pleiades Publishing, Ltd. 2013 |
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Übergeordnetes Werk: |
Enthalten in: Biology bulletin reviews - Moscow : MAIK Nauka/Interperiodica Publ., 2011, 3(2013), 4 vom: Juli, Seite 325-333 |
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Übergeordnetes Werk: |
volume:3 ; year:2013 ; number:4 ; month:07 ; pages:325-333 |
Links: |
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DOI / URN: |
10.1134/S2079086413040051 |
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Katalog-ID: |
SPR031374905 |
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520 | |a Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. | ||
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650 | 4 | |a evolutionary theory of aging |7 (dpeaa)DE-He213 | |
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10.1134/S2079086413040051 doi (DE-627)SPR031374905 (SPR)S2079086413040051-e DE-627 ger DE-627 rakwb eng Novikov, E. A. verfasserin aut Ecological and evolutionary preconditions of extended longevity in subterranean rodents 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2013 Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. lifespan (dpeaa)DE-He213 evolutionary theory of aging (dpeaa)DE-He213 subterranean rodents (dpeaa)DE-He213 reproductive skew (dpeaa)DE-He213 Burda, G. aut Enthalten in Biology bulletin reviews Moscow : MAIK Nauka/Interperiodica Publ., 2011 3(2013), 4 vom: Juli, Seite 325-333 (DE-627)647307227 (DE-600)2595495-7 2079-0872 nnns volume:3 year:2013 number:4 month:07 pages:325-333 https://dx.doi.org/10.1134/S2079086413040051 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 3 2013 4 07 325-333 |
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10.1134/S2079086413040051 doi (DE-627)SPR031374905 (SPR)S2079086413040051-e DE-627 ger DE-627 rakwb eng Novikov, E. A. verfasserin aut Ecological and evolutionary preconditions of extended longevity in subterranean rodents 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2013 Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. lifespan (dpeaa)DE-He213 evolutionary theory of aging (dpeaa)DE-He213 subterranean rodents (dpeaa)DE-He213 reproductive skew (dpeaa)DE-He213 Burda, G. aut Enthalten in Biology bulletin reviews Moscow : MAIK Nauka/Interperiodica Publ., 2011 3(2013), 4 vom: Juli, Seite 325-333 (DE-627)647307227 (DE-600)2595495-7 2079-0872 nnns volume:3 year:2013 number:4 month:07 pages:325-333 https://dx.doi.org/10.1134/S2079086413040051 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 3 2013 4 07 325-333 |
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10.1134/S2079086413040051 doi (DE-627)SPR031374905 (SPR)S2079086413040051-e DE-627 ger DE-627 rakwb eng Novikov, E. A. verfasserin aut Ecological and evolutionary preconditions of extended longevity in subterranean rodents 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2013 Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. lifespan (dpeaa)DE-He213 evolutionary theory of aging (dpeaa)DE-He213 subterranean rodents (dpeaa)DE-He213 reproductive skew (dpeaa)DE-He213 Burda, G. aut Enthalten in Biology bulletin reviews Moscow : MAIK Nauka/Interperiodica Publ., 2011 3(2013), 4 vom: Juli, Seite 325-333 (DE-627)647307227 (DE-600)2595495-7 2079-0872 nnns volume:3 year:2013 number:4 month:07 pages:325-333 https://dx.doi.org/10.1134/S2079086413040051 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 3 2013 4 07 325-333 |
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10.1134/S2079086413040051 doi (DE-627)SPR031374905 (SPR)S2079086413040051-e DE-627 ger DE-627 rakwb eng Novikov, E. A. verfasserin aut Ecological and evolutionary preconditions of extended longevity in subterranean rodents 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2013 Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. lifespan (dpeaa)DE-He213 evolutionary theory of aging (dpeaa)DE-He213 subterranean rodents (dpeaa)DE-He213 reproductive skew (dpeaa)DE-He213 Burda, G. aut Enthalten in Biology bulletin reviews Moscow : MAIK Nauka/Interperiodica Publ., 2011 3(2013), 4 vom: Juli, Seite 325-333 (DE-627)647307227 (DE-600)2595495-7 2079-0872 nnns volume:3 year:2013 number:4 month:07 pages:325-333 https://dx.doi.org/10.1134/S2079086413040051 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 3 2013 4 07 325-333 |
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10.1134/S2079086413040051 doi (DE-627)SPR031374905 (SPR)S2079086413040051-e DE-627 ger DE-627 rakwb eng Novikov, E. A. verfasserin aut Ecological and evolutionary preconditions of extended longevity in subterranean rodents 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Pleiades Publishing, Ltd. 2013 Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. lifespan (dpeaa)DE-He213 evolutionary theory of aging (dpeaa)DE-He213 subterranean rodents (dpeaa)DE-He213 reproductive skew (dpeaa)DE-He213 Burda, G. aut Enthalten in Biology bulletin reviews Moscow : MAIK Nauka/Interperiodica Publ., 2011 3(2013), 4 vom: Juli, Seite 325-333 (DE-627)647307227 (DE-600)2595495-7 2079-0872 nnns volume:3 year:2013 number:4 month:07 pages:325-333 https://dx.doi.org/10.1134/S2079086413040051 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 3 2013 4 07 325-333 |
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Enthalten in Biology bulletin reviews 3(2013), 4 vom: Juli, Seite 325-333 volume:3 year:2013 number:4 month:07 pages:325-333 |
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Novikov, E. A. |
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Novikov, E. A. misc lifespan misc evolutionary theory of aging misc subterranean rodents misc reproductive skew Ecological and evolutionary preconditions of extended longevity in subterranean rodents |
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Ecological and evolutionary preconditions of extended longevity in subterranean rodents lifespan (dpeaa)DE-He213 evolutionary theory of aging (dpeaa)DE-He213 subterranean rodents (dpeaa)DE-He213 reproductive skew (dpeaa)DE-He213 |
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Ecological and evolutionary preconditions of extended longevity in subterranean rodents |
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Ecological and evolutionary preconditions of extended longevity in subterranean rodents |
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ecological and evolutionary preconditions of extended longevity in subterranean rodents |
title_auth |
Ecological and evolutionary preconditions of extended longevity in subterranean rodents |
abstract |
Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. © Pleiades Publishing, Ltd. 2013 |
abstractGer |
Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. © Pleiades Publishing, Ltd. 2013 |
abstract_unstemmed |
Abstract According to the evolutionary theory of aging, a low level of extrinsic mortality, i.e., a low probability of the early death of animals, promotes an increase in the maximum lifespan. The subterranean rodents that dwell in well-protected environment, live longer than the terrestrial species. In the social African mole rat species with reproductive division of labor, the mortality of workers in wildlife is considerably higher than in breeders, while significant interspecific differences in the lifespan patterns may emerge in captivity. The lifespans of different castes in the family groups of the naked mole rat (Heterocephalus glaber) in captivity are almost equal. However, the breeders of another social species, the Ansell’s mole rat (Fukomys anselli), on the average live twice as long as workers. A possible explanation for the observed differences can be associated with the species specificity in their social organization, first and foremost, the mechanisms responsible for reproductive skew. A unique feature of the naked mole rat is tolerance for incest, which theoretically equalizes the chances of all individuals to be a breeder within the native family. In other social mole rat species, which avoids inbreeding, the only possibility for reproduction is dispersal. In captivity, the inability to leave the maternal family may cause the suppression of homeostatic functions responsible for longevity. © Pleiades Publishing, Ltd. 2013 |
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container_issue |
4 |
title_short |
Ecological and evolutionary preconditions of extended longevity in subterranean rodents |
url |
https://dx.doi.org/10.1134/S2079086413040051 |
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author2 |
Burda, G. |
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doi_str |
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up_date |
2024-07-03T23:25:34.725Z |
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