Home About us Contact | |||
Somatic Maintenance (somatic + maintenance)
Selected AbstractsCALORIE RESTRICTION AND AGING: A LIFE-HISTORY ANALYSISEVOLUTION, Issue 3 2000Daryl P. Shanley Abstract., The disposable soma theory suggests that aging occurs because natural selection favors a strategy in which fewer resources are invested in somatic maintenance than are necessary for indefinite survival. However, laboratory rodents on calorie-restricted diets have extended life spans and retarded aging. One hypothesis is that this is an adaptive response involving a shift of resources during short periods of famine away from reproduction and toward increased somatic maintenance. The potential benefit is that the animal gains an increased chance of survival with a reduced intrinsic rate of senescence, thereby permitting reproductive value to be preserved for when the famine is over. We describe a mathematical life-history model of dynamic resource allocation that tests this idea. Senescence is modeled as a change in state that depends on the resources allocated to maintenance. Individuals are assumed to allocate the available resources to maximize the total number of descendants. The model shows that the evolutionary hypothesis is plausible and identifies two factors, both likely to exist, that favor this conclusion. These factors are that survival of juveniles is reduced during periods of famine and that the organism needs to pay an energetic "overhead" before any litter of offspring can be produced. If neither of these conditions holds, there is no evolutionary advantage to be gained from switching extra resources to maintenance. The model provides a basis to evaluate whether the life-extending effects of calorie-restriction might apply in other species, including humans. [source] Test of a developmental trade-off in a polyphenic butterfly: direct development favours reproductive outputFUNCTIONAL ECOLOGY, Issue 1 2008Bengt Karlsson Summary 1Evolutionary theory predicts that resource allocation decisions taken during development are adjusted to an organism's life-history. These decisions may have irreversible effects on body design and strong fitness consequences. Holometabolous insects that have a long expected life span typically postpone reproduction, and so are expected to allocate resources for somatic maintenance prior to investing in reproduction. In contrast, insects that have a short expected life span are expected to allocate relatively less to soma and more to reproduction. In support of this theory, an earlier investigation of resources allocated to soma vs. reproductive reserves in the comma butterfly, Polygonia c-album, revealed that short-lived females indeed allocate more resources to reproductive reserves as compared to longer lived females that hibernate before reproduction suggesting that short-lived females should have higher fecundity. 2Here we test this prediction, using the comma butterfly as our study organism. Depending on daylength and temperature this butterfly produces one of two morphs: (i) a light summer morph that reproduces directly after adult eclosion and has a short expected life span of a couple of weeks; or (ii) a darker winter morph that normally lives for 8,9 months before the onset of reproduction. Our test is based on experimental manipulation that allowed us to induce reproduction without prior hibernation in winter morph comma butterflies, and comparing lifetime fecundity among three groups: (i) directly reproducing summer morph commas; (ii) directly reproducing winter morph commas; and (iii) winter morph commas reproducing after overwintering. This protocol allowed us to tease apart trade-offs during development and the hibernation period. 3The results showed that the short-lived summer morph had a substantially higher fecundity (total number of eggs = 586 ± 19, mean ± SE) than the winter morph females manipulated to reproduce without hibernation (total number of eggs = 334 ± 42). We argue that this is a consequence of a resource allocation trade-off during early development observed in this species; females with a short expected life as adults allocate relatively more of their resources to reproductive parts and thereby reach a higher reproductive output compared to females predisposed for a long adult life. 4There was no significant difference in lifetime fecundity between winter morph females that did, or did not, hibernate before reproduction. This suggests that the cost of hibernation per se is small and hence corroborates our conclusion that the life-history implemented trade-off made during early development underlies the lower reproductive output of the winter morph butterflies. [source] Women's fertility and mortality in late mid life: A comparison of three contemporary populationsAMERICAN JOURNAL OF HUMAN BIOLOGY, Issue 4 2009Emily Grundy Evolutionary theory suggests a trade-off between reproduction and somatic maintenance implying a negative relationship between parity and longevity, at least in natural fertility populations. In populations in which fertility control is usual, there are also a number of mechanisms that may link reproductive careers and later mortality, but evidence of associations between women's fertility patterns and their later life health has been judged inconclusive due to varying controls for socio-economic characteristics and marital status. Here, we build on three recent studies that followed a common framework to investigate associations between women's parity and timing of first and last birth with mortality in late middle age in three contemporary developed counties, Norway, England and Wales, and the USA. Data were drawn from whole population registers (Norway); a large census-based record linkage study (England and Wales), and a nationally representative survey linked to death records (USA). Results show that teenage childbirth was associated with higher mortality risks in late middle age in all three countries. Risks of death were significantly raised among nulliparous women in Norway and England and Wales, and also raised (although not significantly so) for childless US women. However, although higher parity was associated with a slight mortality disadvantage in England and Wales and the USA, the reverse seemed the case in Norway. These finding suggest that in populations in which fertility control is usual, contextual factors influencing the relative costs and benefits of childbearing may influence associations between fertility histories and later mortality. Am. J. Hum. Biol., 2009. © 2009 Wiley-Liss, Inc. [source] The effects of lactation and infant care on adult energy budgets in wild siamangs (Symphalangus syndactylus)AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, Issue 2 2009Susan Lappan Abstract In mammals with biparental care of offspring, males and females may bear substantial energetic costs of reproduction. Adult strategies to reduce energetic stress include changes in activity patterns, reduced basal metabolic rates, and storage of energy prior to a reproductive attempt. I quantified patterns of behavior in five groups of wild siamangs (Symphalangus syndactylus) to detect periods of high energetic investment by adults and to examine the relationships between infant care and adult activity patterns. For females, the estimated costs of lactation peaked at around infant age 4,6 months and were low by infant age 1 year, whereas the estimated costs of infant-carrying peaked between ages 7 and 12 months, and approached zero by age 16 months. There was a transition from primarily female to male care in the second year of life in some groups. Females spent significantly less time feeding during lactation than during the later stages of infant care, suggesting that female siamangs do not use increased food intake to offset the costs of lactation. Female feeding time was highest between infant ages 16 and 21 months, a period of relatively low female investment in the current offspring that coincided with the period of highest male investment in infant care. This suggests that male care may reduce the costs of infant care for females in the later stages of a reproductive attempt. The female energy gain resulting from male care was likely invested in somatic maintenance and future reproduction, rather than the current offspring. Am J Phys Anthropol, 2009. © 2009 Wiley-Liss, Inc. [source] |