Старение. Почему эволюция убивает? - Петр Владимирович Лидский

77. Harvanek Z. M., Lyu Y., Gendron C. M., Johnson J. C., Kondo S., Promislow D. E. L., et al. Perceptive costs of reproduction drive ageing and physiology in male Drosophila. Nature Ecology Evolution. 2017; 1(6):0152. doi: 10.1038/s41559−017–0152.

78. Westendorp R. G., Kirkwood T. B. Human longevity at the cost of reproductive success. Nature. 1998; 396(6713):743−6. doi: 10.1038/25519. PubMed PMID: 9874369.

79. Gavrilov L. A., Gavrilova N. S. Is There a Reproductive Cost for Human Longevity? Journal of Anti-Aging Medicine. 1999; 2(2):121−3. doi: 10.1089/rej.1.1999.2.121.

80. Mitchell S. E., Simpson M., Coulet L., Gouedard S., Hambly C., Morimoto J., et al. Reproduction has immediate effects on female mortality, but no discernible lasting physiological impacts: A test of the disposable soma theory. Proceedings of the National Academy of Sciences. 2024; 121(42):e2408682121.

81. Bower J. R., Noro K., Sakurai Y., Scheel D. Chapter 21 — Enteroctopus dofleini, Giant Pacific octopus. In: Rosa R, Gleadall IG, Pierce GJ, Villanueva R, editors. Octopus Biology and Ecology: Academic Press; 2024. p. 369–95.

82. Podlutsky A. J., Khritankov A. M., Ovodov N. D., Austad S. N. A new field record for bat longevity. J Gerontol A Biol Sci Med Sci. 2005; 60(11):1366−8. doi: 10.1093/gerona/60.11.1366. PubMed PMID: 16339320.

83. Wilkinson G. S., Adams D. M. Recurrent evolution of extreme longevity in bats. Biology letters. 2019; 15(4):20180860.

84. Geiser F., Stawski C. Hibernation and Torpor in Tropical and Subtropical Bats in Relation to Energetics, Extinctions, and the Evolution of Endothermy. Integrative and Comparative Biology. 2011; 51(3):337–48. doi: 10.1093/icb/icr042.

85. Austad S. N., Finch C. E. How ubiquitous is aging in vertebrates? Science. 2022; 376(6600):1384–5. doi: doi:10.1126/science.adc9442.

86. Wensink M. J., Caswell H., Baudisch A. The Rarity of Survival to Old Age Does Not Drive the Evolution of Senescence. Evol Biol. 2017; 44(1):5–10. Epub 20160504. doi: 10.1007/s11692−016–9385−4. PubMed PMID: 28280278; PubMed Central PMCID: PMCPMC5321711.

87. Moorad J., Promislow D., Silvertown J. Evolutionary Ecology of Senescence and a Reassessment of Williams' «Extrinsic Mortality» Hypothesis. Trends in Ecology Evolution. 2019;34(6):519−30. doi: https://doi.org/10.1016/j. tree.2019.02.006.

88. Reznick D. N., Bryant M. J., Roff D., Ghalambor C. K., Ghalambor D. E. Effect of extrinsic mortality on the evolution of senescence in guppies. Nature. 2004; 431(7012):1095−9. doi: 10.1038/nature02936.

89. Chen H. Y., Maklakov A. A. Longer life span evolves under high rates of condition-dependent mortality. Curr Biol. 2012; 22(22):2140–3. Epub 20121018. doi: 10.1016/j. cub.2012.09.021. PubMed PMID: 23084993.

90. Austad S. N. Retarded senescence in an insular population of Virginia opossums (Didelphis virginiana). Journal of Zoology. 1993; 229(4):695–708. doi: https://doi.org/10.1111/j.1469–7998.1993.tb02665.x.

91. de Vries C., Galipaud M., Kokko H. Extrinsic mortality and senescence: a guide for the perplexed. Peer Community Journal. 2023; 3.

92. Sandercock B. K., Jaramillo A. Annual Survival Rates of Wintering Sparrows: Assessing Demographic Consequences of Migration. The Auk. 2002; 119(1):149–65. doi: 10.1093/auk/119.1.149.

93. Pinho G. M., Martin J. G. A., Farrell C., Haghani A., Zoller J. A., Zhang J., et al. Hibernation slows epigenetic ageing in yellow-bellied marmots. Nature Ecology Evolution. 2022;6(4):418–26. doi: 10.1038/s41559−022–01679−1.

94. Turbill C., Bieber C., Ruf T. Hibernation is associated with increased survival and the evolution of slow life histories among mammals. Proceedings of the Royal Society B: Biological Sciences. 2011; 278(1723):3355−63. doi: doi:10.1098/rspb.2011.0190.

95. Wikipedia. Brandt’s bat (Myotis brandtii) 2025.

96. Funakoshi K. The longest life span based on the re-occupation record of Murina ussuriensis. Nature of Kagoshima. 2020; 47:47–39.

97. Kerepesi C., Meer M. V., Ablaeva J., Amoroso V. G., Lee S.-G., Zhang B., et al. Epigenetic aging of the demographically non-aging naked mole-rat. Nature Communications. 2022; 13(1):355. doi: 10.1038/s41467−022–27959−9.

98. Braude S. The behavior and demographics of the naked mole-rat, Heterocephalus glaber [Ph. D.]. United States — Michigan: University of Michigan; 1991.

99. Kerr P. J., Liu J., Cattadori I., Ghedin E., Read A. F., Holmes E. C. Myxoma Virus and the Leporipoxviruses: An Evolutionary Paradigm. Viruses [Internet]. 2015; 7(3):[1020−61 pp.].

100. Anderson R. M., May R. M. Coevolution of hosts and parasites. Parasitology. 1982; 85(2):411−26. Epub 2009/04/06. doi: 10.1017/S0031182000055360.

101. Enard D., Cai L., Gwennap C., Petrov D. A. Viruses are a dominant driver of protein adaptation in mammals. eLife. 2016; 5:e12469. doi: 10.7554/eLife.12469.

102. Halvorsen O., Andersen K. The ecological interaction between arctic charr, Salvelinus alpinus (L.), and the plerocercoid stage of Diphyllobothrium ditremum. Journal of Fish Biology. 1984; 25(3):305–16. doi: https://doi.org/10.1111/j.1095–8649.1984.tb04878.x.

103. Lachish S., Miller K. J., Storfer A., Goldizen A. W., Jones M. E. Evidence that disease-induced population decline changes genetic structure and alters dispersal patterns in the Tasmanian devil. Heredity. 2011; 106(1):172–82. doi: 10.1038/hdy.2010.17.

104. Miller M. B., Bassler B. L. Quorum Sensing in Bacteria. Annual Review of Microbiology. 2001; 55(Volume 55, 2001):165–99. doi: https://doi.org/10.1146/annurev.micro.55.1.165.

105. Matthysen E. Density-dependent dispersal in birds and mammals. Ecography. 2005; 28(3):403–16. doi: https://doi.org/10.1111/j.0906–7590.2005.04073.x.

106. Lopatina A., Tal N., Sorek R. Abortive Infection: Bacterial Suicide as an Antiviral Immune Strategy. Annu Rev Virol. 2020; 7(1):371–84. Epub 20200619. doi: 10.1146/annurev-virology-011620–040628. PubMed PMID: 32559405.

107. Beros S., Lenhart A., Scharf I., Negroni M. A., Menzel F., Foitzik S. Extreme lifespan extension in tapeworm-infected ant workers. Royal Society Open Science. 2021; 8(5):202118. doi: doi:10.1098/rsos.202118.

108. Beani L., Dallai R., Cappa F., Manfredini F., Zaccaroni M., Lorenzi M. C., et al. A Strepsipteran parasite extends the lifespan of workers in a social wasp. Scientific Reports. 2021; 11(1):7235. doi: 10.1038/s41598−021–86182–6.

109. Azevedo Jd. S., Silva L. Gd., Bizerri C. R. S. F, Dansa-Petretski M. A., Lima N. R. W. Infestation pattern and parasitic castration of the crustacean Riggia paranensis (Crustacea: Cymothoidea) on the fresh water fish Cyphocharax gilbert (Teleostei: Curimatidae). Neotropical Ichthyology. 2006; 4.

110. Hurd H., Warr E., Polwart A. A parasite that increases host lifespan. Proceedings of the Royal Society of London Series B: Biological Sciences. 2001; 268(1477):1749–53. doi: doi:10.1098/rspb.2001.1729.

111. Minchella D. J., Leathers B. K., Brown K. M., McNair J. N. Host and Parasite Counteradaptations: An Example from a Freshwater Snail. The American Naturalist. 1985; 126(6):843−54. doi: 10.1086/284456.

112. Libert S., Chao Y., Chu X., Pletcher S. D. Trade-offs between longevity and pathogen resistance in Drosophila melanogaster are mediated by NFkappaB signaling. Aging Cell. 2006; 5(6):533–43. doi: 10.1111/j.1474–9726.2006.00251.x. PubMed PMID: 17129215.

113. Tomusiak A., Floro A., Tiwari R., Riley R., Matsui H., Andrews N., et