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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

different. Fig. 11.4 displays the average age-specific fertilities for three hunter-gatherer populations and the conservative age-specific fertility schedule synthesized from six wild chimpanzee populations by M. Emery Thompson and others (2007). Human populations can differ widely in fertility levels, but among them—hunter-gatherers included—the change in the rate of babies born to women of each age has a familiar peaked shape. “[I]n all populations where reliable records have been kept, fertility is zero until about age 15, rises smoothly to a single peak, and falls smoothly to zero by age 45–50” (Coale and Demeny, 1983, p. 27). The fertility schedule for wild chimpanzees is flat-topped instead. The rate reached before the age of 20 continues with little change for two more decades.

The percentages running along the horizontal axis in Fig. 11.4 show the relative size of each age class compared to the first age class of

FIGURE 11.4 Age-specific fertility rates (ASFR) for humans and chimpanzees. Humans (open circles) are represented by the average of three hunter-gatherer populations: !Kung Bushmen of Botswana (Hill and Hurtado, 1996), Ache of Paraguay (Hill and Hurtado, 1996), and Hadza of Tanzania (Blurton Jones et al., 2002). Estimates for chimpanzees in the wild (closed squares) come from the conservative fertility schedule synthesized from six study sites by Emery Thompson et al. (2007). The bumps reflect small sample size (627 risk years in the initial chimpanzee adult age class declining to 8 risk years in the 45- to 49-year interval (Emery Thompson et al., 2007, supplementary table 2). The percentages along the horizontal axis indicate the proportion of those reaching adulthood that survive to the age class. The top row of percentages comprises estimates for chimpanzees from the number of risk years in each age class (Emery Thompson et al., 2007, supplementary table 2). They are just slightly lower than the model in Fig. 11.1 from the life table (Hill et al., 2001). The bottom row comprises human estimates from the female life table for Hadza hunter-gatherers (Blurton Jones et al., 2002).

FIGURE 11.4 Age-specific fertility rates (ASFR) for humans and chimpanzees. Humans (open circles) are represented by the average of three hunter-gatherer populations: !Kung Bushmen of Botswana (Hill and Hurtado, 1996), Ache of Paraguay (Hill and Hurtado, 1996), and Hadza of Tanzania (Blurton Jones et al., 2002). Estimates for chimpanzees in the wild (closed squares) come from the conservative fertility schedule synthesized from six study sites by Emery Thompson et al. (2007). The bumps reflect small sample size (627 risk years in the initial chimpanzee adult age class declining to 8 risk years in the 45- to 49-year interval (Emery Thompson et al., 2007, supplementary table 2). The percentages along the horizontal axis indicate the proportion of those reaching adulthood that survive to the age class. The top row of percentages comprises estimates for chimpanzees from the number of risk years in each age class (Emery Thompson et al., 2007, supplementary table 2). They are just slightly lower than the model in Fig. 11.1 from the life table (Hill et al., 2001). The bottom row comprises human estimates from the female life table for Hadza hunter-gatherers (Blurton Jones et al., 2002).

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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)