期刊
METHODS IN ECOLOGY AND EVOLUTION
卷 2, 期 5, 页码 446-453出版社
WILEY
DOI: 10.1111/j.2041-210X.2011.00095.x
关键词
demography; life-history evolution; life-table methods; menopause; primates; simulation; Type I error
类别
资金
- Max Planck Society
- Ruth L. Kirschstein National Research Service Award (NIA) [T32-AG000246]
- Museum of Vertebrate Zoology
- [P01 AG022500]
1. While classical life-history theory does not predict postreproductive life span (PRLS), it has been detected in a great number of taxa, leading to the view that it is a broadly conserved trait and attempts to reconcile theory with these observations. We suggest an alternative: the apparently wide distribution of significant PRLS is an artefact of insufficient methods. 2. PRLS is traditionally measured in units of time between each individual's last parturition and death, after excluding those individuals for whom this interval is short. A mean of this measure is then calculated as a population value. We show this traditional population measure (which we denote PrT) to be inconsistently calculated, inherently biased, strongly correlated with overall longevity, uninformative on the importance of PRLS in a population's life history, unable to use the most commonly available form of relevant data and without a realistic null hypothesis. Using data altered to ensure that the null hypothesis is true, we find a false-positive rate of 0 47 for PrT. 3. We propose an alternative population measure, using life-table methods. Postreproductive representation (PrR) is the proportion of adult years lived which are postreproductive. We briefly derive PrR and discuss its properties. We employ a demographic simulation, based on the null hypothesis of simultaneous and proportional decline in survivorship and fecundity, to produce a null distribution for PrR based on the age-specific rates of a population. 4. In an example analysis, using data on 84 populations of human and nonhuman primates, we demonstrate the ability of PrR to represent the effects of artificial protection from mortality and of humanness on PRLS. PrR is found to be higher for all human populations under a wide range of conditions than for any nonhuman primate in our sample. A strong effect of artificial protection is found, but humans under the most adverse conditions still achieve PrR of >0.3. 5. PrT should not be used as a population measure and should be used as an individual measure only with great caution. The use of PrRas an intuitive, statistically valid and intercomparable population life-history measure is encouraged.
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