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1.
Mol Ecol ; 22(1): 249-59, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23167566

ABSTRACT

Explaining variation in life expectancy between individuals of the same age is fundamental to our understanding of population ecology and life history evolution. Variation in the length and rate of loss of the protective telomere chromosome caps has been linked to cellular lifespan. Yet, the extent to which telomere length and dynamics predict organismal lifespan in nature is still contentious. Using longitudinal samples taken from a closed population of Acrocephalus sechellensis (Seychelles warblers) studied for over 20 years, we describe the first study into life-long adult telomere dynamics (1-17 years) and their relationship to mortality under natural conditions (n = 204 individuals). We show that telomeres shorten with increasing age and body mass, and that shorter telomeres and greater rates of telomere shortening predicted future mortality. Our results provide the first clear and unambiguous evidence of a relationship between telomere length and mortality in the wild, and substantiate the prediction that telomere length and shortening rate can act as an indicator of biological age further to chronological age when exploring life history questions in natural conditions.


Subject(s)
Aging/genetics , Songbirds/genetics , Telomere Shortening , Animals , Female , Genetic Variation , Longevity/genetics , Longitudinal Studies , Male
2.
Aging Cell ; 10(6): 913-21, 2011 Dec.
Article in English | MEDLINE | ID: mdl-21902801

ABSTRACT

Males and females often age at different rates resulting in longevity 'gender gaps', where one sex outlives the other. Why the sexes have different lifespans is an age-old question, still fiercely debated today. One cellular process related to lifespan, which is known to differ according to sex, is the rate at which the protective telomere chromosome caps are lost. In humans, men have shorter lifespans and greater telomere shortening. This has led to speculation in the medical literature that sex-specific telomere shortening is one cause of sex-specific mortality. However, telomere shortening may be a cause for and/or a consequence of the processes that govern survival, and to infer general principles from single-taxon studies may be misleading. Here, we review recent work on telomeres in a variety of animal taxa, including those with reverse sexual lifespan dimorphism (i.e., where males live longer), to establish whether sex-specific survival is generally associated with sex differences in telomere dynamics. By doing this, we attempt to tease apart the potential underlying causes for sex differences in telomere lengths in humans and highlight targets for future research across all taxa.


Subject(s)
Hormones/genetics , Life Expectancy , Longevity/genetics , Telomere Shortening , Telomere/metabolism , Animals , Female , Germ Cells/cytology , Humans , Male , Oxidative Stress , Sex Characteristics , Sex Factors , Telomere/chemistry
3.
Proc Biol Sci ; 276(1671): 3257-64, 2009 Sep 22.
Article in English | MEDLINE | ID: mdl-19553255

ABSTRACT

We have yet to understand fully how conditions during different periods of development interact to influence life-history structure. Can the negative effects of poor juvenile nutrition be overcome by a good adult diet, or are life-history strategies set by early experience? Here, we tested the influence and interaction of different nutritional quality during juvenile and sexual development on female resource allocation physiology, life history and courtship behaviour in the cockroach, Nauphoeta cinerea. Nymphs were raised on either a good-quality or poor-quality diet. After adult eclosion, females were either switched to the opposite diet or remained on their original diet. We assessed mating behaviour and lifetime reproductive success for half of the females from each treatment. We evaluated reproductive investment, somatic investment and resource reallocation from reproduction to the soma via oocyte apoptosis in the remaining females. We found that poor juvenile conditions resulted in a fat phenotype with slow juvenile growth and short reproductive lifespan that could not be retrieved with a change in diet. Good juvenile conditions resulted in the converse, but again fixed, phenotype in adulthood. Thus, juvenile nutrition sets adult patterns of resource allocation.


Subject(s)
Cockroaches/growth & development , Animal Nutritional Physiological Phenomena , Animals , Cockroaches/metabolism , Cockroaches/physiology , Feeding Behavior , Female , Male , Nymph/growth & development , Nymph/metabolism , Nymph/physiology , Phenotype , Reproduction , Sexual Behavior, Animal
4.
J Insect Physiol ; 54(1): 25-31, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17826791

ABSTRACT

Ovarian apoptosis has been found to occur in the female cockroach Nauphoeta cinerea in response to lack of mates. It has been proposed that ovarian apoptosis in continuously breeding insects is an adaptive mechanism for recouping resources in poor conditions (oosorption). However, N. cinerea is a cyclically breeding insect and ovarian apoptosis may represent ageing and clearance of old unused oocytes. To test the hypothesis that oocyte resorption via apoptosis reflects the reclamation of resources, we delayed mating in combination with positive and negative nutritional signals. Females without access to food during sexual maturation invested less in reproduction and had elevated rates of ovarian apoptosis in the terminal oocyte. Starvation also induced apoptosis in non-vitellogenic oocytes of the vitellarium and germinarium, which would be used for future reproductive events. This is paradoxical as theory states that oosorption is an adaptive means of rerouting resources into investment in future reproduction, yet these oocytes do not represent a cache of resources and their loss could limit future reproduction.


Subject(s)
Animal Nutritional Physiological Phenomena/physiology , Apoptosis/physiology , Cockroaches/physiology , Ovary/physiology , Sexual Behavior, Animal/physiology , Animals , Body Weight , Female , Oocytes/cytology
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