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In the Light of Evolution IV: The Human Condition (2010)
National Research Council (NRC)

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. "11 How Grandmother Effects Plus Individual Variation in Frailty Shape Fertility and Mortality: Guidance from Human-Chimpanzee Comparisons--Kristen Hawkes ." In the Light of Evolution IV: The Human Condition. Washington, DC: The National Academies Press, 2010.

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In the Light of Evolution Volume IV: The Human Condition

very like those observed in hunter-gatherers are maintained by selection against deleterious mutations (Lee, 2008).

AGE STRUCTURES

Our grandmother hypothesis relies on Charnov’s model of life history evolution (Charnov, 1991, 1993) to explain how correlated allometries in mammalian life history features apply to humans (Hawkes et al., 1998; Alvarez, 2000). Comparisons between other great apes and humans (Robson et al., 2006) have been essential in highlighting distinctive human life history features. As noted, chimpanzees are an especially important comparative model for phylogenetic, ecological, and morphological reasons. Fig. 11.1 shows the female side of the age structure for a human hunter-gatherer population and wild chimpanzees modeled from life tables.

FIGURE 11.1 Female age structures modeled from life tables. Each bar shows the percentage of the population in the 5-year age class indicated in the vertical axis. Lightest bars, juvenile years; medium-gray bars, childbearing years; darkest bars, post-fertile years. Humans are on the right, represented by Hadza huntergatherers with Blurton Jones’s (2002) data. In this population, life expectancy at birth is 33 years. With growth rate 1.3%/year, 32% of the women (those over 15) are past the age of 45. Growing populations are younger because more are born than die. If this population was stationary, the percentage of adult women past the age of 45 would be 39% (Hawkes and Blurton Jones, 2005). The left side of the figure represents the synthetic wild chimpanzee population constructed by Hill and colleagues (2000) using data from five wild study sites. Average age at first birth is 13 in wild chimpanzees so the 10- to 14-year age class is included in the childbearing years. Fertility ends by ~45 in both species. Less than 3% of the adult chimpanzees (counted as those over 10 years) are past the age of 45. The chimpanzee model assumes a stationary population.

FIGURE 11.1 Female age structures modeled from life tables. Each bar shows the percentage of the population in the 5-year age class indicated in the vertical axis. Lightest bars, juvenile years; medium-gray bars, childbearing years; darkest bars, post-fertile years. Humans are on the right, represented by Hadza huntergatherers with Blurton Jones’s (2002) data. In this population, life expectancy at birth is 33 years. With growth rate 1.3%/year, 32% of the women (those over 15) are past the age of 45. Growing populations are younger because more are born than die. If this population was stationary, the percentage of adult women past the age of 45 would be 39% (Hawkes and Blurton Jones, 2005). The left side of the figure represents the synthetic wild chimpanzee population constructed by Hill and colleagues (2000) using data from five wild study sites. Average age at first birth is 13 in wild chimpanzees so the 10- to 14-year age class is included in the childbearing years. Fertility ends by ~45 in both species. Less than 3% of the adult chimpanzees (counted as those over 10 years) are past the age of 45. The chimpanzee model assumes a stationary population.

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Front Matter (R1-R16)
PART I: HUMAN PHYLOGENETIC HISTORY AND THE PALEONTOLOGICAL RECORD (1-4)
1 Reconstructing Human Evolution: Achievements, Challenges, and Opportunities--Bernard Wood (5-26)
2 Terrestrial Apes and Phylogenetic Trees--Juan Luis Arsuaga (27-46)
3 Phylogenomic Evidence of Adaptive Evolution in the Ancestry of Humans-Morris Goodman and Kirstin N. Sterner (47-62)
4 Human Adaptations to Diet, Subsistence, and Ecoregion Are Due to Subtle Shifts in Allele Frequency--Angela M. Hancock, David B. Witonsky, Edvard Ehler, Gorka Alkorta-Aranburu, Cynthia Beall, Amha Gebremedhin, Rem Sukernik, Gerd Utermann, Jonathan Pritchard, Graham Coop, and Anna Di Rienzo (63-80)
5 Working Toward a Synthesis of Archaeological, Linguistic, and Genetic Data for Inferring African Population History--Laura B. Scheinfeldt, Sameer Soi, and Sarah A. Tishkoff (81-100)
PART II: STRUCTURE AND FUNCTION OF THE HUMAN GENOME (101-104)
6 Uniquely Human Evolution of Sialic Acid Genetics and Biology--Ajit Varki (105-126)
7 Bioenergetics, the Origins of Complexity, and the Ascent of Man-Douglas C. Wallace (127-146)
8 Genome-wide Patterns of Population Structure and Admixture Among Hispanic/Latino Populations--Katarzyna Bryc, Christopher Velez, Tatiana Karafet, Andres Moreno-Estrada, Andy Reynolds, Adam Auton, Michael Hammer, Carlos D. Bustamante, and Harry Ostrer (147-166)
9 Human Skin Pigmentation as an Adaptation to UV Radiation--Nina G. Jablonski and George Chaplin (167-184)
10 Footprints of Nonsentient Design Inside the Human Genome--John C. Avise (185-204)
PART III: CULTURAL EVOLUTION AND THE UNIQUENESS OF BEING HUMAN (205-210)
11 How Grandmother Effects Plus Individual Variation in Frailty Shape Fertility and Mortality: Guidance from Human-Chimpanzee Comparisons--Kristen Hawkes (211-230)
12 Gene–Culture Coevolution in the Age of Genomics--Peter J. Richerson, Robert Boyd, and Joseph Henrich (231-256)
13 The Cognitive Niche: Coevolution of Intelligence, Sociality, and Language--Steven Pinker (257-274)
14 A Role for Relaxed Selection in the Evolution of the Language Capacity--Terrence W. Deacon (275-292)
15 Adaptive Specializations, Social Exchange, and the Evolution of Human Intelligence--Leda Cosmides, H. Clark Barrett, and John Tooby (293-318)
16 The Difference of Being Human: Morality--Francisco J. Ayala (319-340)
References (341-392)
Index (393-412)