Evolutionary Senescence Theory.docx Date: 25/05/2025 | Views: 260

Share in :

Evolutionary Senescence Theory
Abstract
The Evolutionary Senescence Theory seeks to explain the biological phenomenon of aging through the lens of natural selection. It proposes that aging is not directly selected for, but results from a decline in the force of natural selection with age. This review synthesizes key models and empirical findings underpinning the theory, particularly focusing on Medawar’s mutation accumulation hypothesis, Williams’ antagonistic pleiotropy, and Kirkwood’s disposable soma theory. Theoretical advancements and critiques are discussed, alongside modern genomic and experimental findings that shape the current understanding of senescence.
1. Introduction
Senescence, defined as the progressive decline in physiological function and increased mortality risk with age, presents a paradox for evolutionary biology. Why would natural selection allow a process that decreases individual fitness? The Evolutionary Senescence Theory (EST) provides a framework for resolving this paradox by emphasizing the age-related decline in the force of selection (Medawar, 1952; Hamilton, 1966).
2. Theoretical Foundations
2.1 Mutation Accumulation Hypothesis
Medawar (1952) postulated that deleterious mutations manifesting later in life can accumulate in a population because their effects occur after reproduction. Since natural selection weakens with age, these mutations are less effectively purged from the gene pool.
2.2 Antagonistic Pleiotropy
Williams (1957) introduced the concept of antagonistic pleiotropy, whereby genes beneficial in early life can have harmful effects in later life. These genes are selected because early-life benefits outweigh late-life costs in terms of reproductive success
2.3 Disposable Soma Theory
Kirkwood (1977) extended the theory by proposing that organisms allocate resources between reproduction and somatic maintenance. Aging results from evolutionary trade-offs where somatic repair is deprioritized in favor of reproduction, leading to gradual deterioration.
3. Empirical Support and Developments
Substantial empirical evidence supports EST. Hamilton's (1966) mathematical models quantified the declining force of natural selection with age. Experimental evolution studies in Drosophila melanogaster have shown that longevity can be increased under selection, consistent with the hypothesis that senescence is malleable (Rose, 1991).
Moreover, genomic studies have identified genes with pleiotropic effects on aging and reproduction (Maklakov & Chapman, 2019). The emergence of comparative genomics has shown variability in senescence patterns across taxa, challenging the universality of aging and refining the theory (Jones et al., 2014).
4. Critiques and Modern Interpretations
While EST remains a dominant framework, it faces criticism. Some organisms, like certain turtles and trees, show negligible senescence (Finch, 1990), prompting discussions on the role of ecology and life history strategies. Recent theories integrate EST with mechanisms of damage accumulation and stress responses (López-Otín et al., 2013).
5. Conclusion
The Evolutionary Senescence Theory has significantly advanced the understanding of aging as an evolutionary byproduct of selection dynamics. Although its core principles remain robust, ongoing research continues to refine the theory, integrating molecular mechanisms and ecological variability. A pluralistic approach that incorporates EST with emerging biological insights offers the most promising route forward.

References
Finch, C. E. (1990). Longevity, Senescence, and the Genome. University of Chicago Press.
Hamilton, W. D. (1966). The moulding of senescence by natural selection. Journal of Theoretical Biology, 12(1), 12–45. https://doi.org/10.1016/0022-5193(66)90184-6
Jones, O. R., et al. (2014). Diversity of ageing across the tree of life. Nature, 505(7482), 169–173. https://doi.org/10.1038/nature12789
Kirkwood, T. B. L. (1977). Evolution of ageing. Nature, 270(5635), 301–304. https://doi.org/10.1038/270301a0
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2013). The hallmarks of aging. Cell, 153(6), 1194–1217. https://doi.org/10.1016/j.cell.2013.05.039
Maklakov, A. A., & Chapman, T. (2019). Evolution of ageing as a tangle of trade-offs: Energy versus function. Proceedings of the Royal Society B, 286(1911), 20191604. https://doi.org/10.1098/rspb.2019.1604
Medawar, P. B. (1952). An Unsolved Problem of Biology. H.K. Lewis.
Rose, M. R. (1991). Evolutionary Biology of Aging. Oxford University Press.Williams, G. C. (1957). Pleiotropy, natural selection, and the evolution of senescence. Evolution, 11(4), 398–411. https://doi.org/10.2307/2406060


Written by Professor Dr. Aqeel Al Jothery (PhD UK).
Anesthesia Techniques Department, College of Health and Medical Technologies, Al-Mustaqbal University

Al-Mustaqbal University is the first university in Iraq