Lucio Vinicius
University College London, Evolutionary Anthropology, Faculty Member
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... Modular Evolution How Natural Selection Produces Biological Complexity lucio vinicius Leverhulme Centre for Human Evolutionary Studies, Cambridge ... New York www.cambridge.org Information on this title:... more
... Modular Evolution How Natural Selection Produces Biological Complexity lucio vinicius Leverhulme Centre for Human Evolutionary Studies, Cambridge ... New York www.cambridge.org Information on this title: www.cambridge.org/9780521429641 © l. vinicius Castilho 2010 This ...
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Post-reproductive lifespans (PRLSs) of men vary across traditional societies. We argue that if sexual selection operates on male age-dependent resource availability (or 'reproductive market... more
Post-reproductive lifespans (PRLSs) of men vary across traditional societies. We argue that if sexual selection operates on male age-dependent resource availability (or 'reproductive market values') the result is variation in male late-life reproduction across subsistence systems. This perspective highlights the uniqueness of PRLS in both women and men.
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Research Interests: Evolutionary Biology, Mathematics, Archaeology, Anthropology, Human Evolution, and 19 moreAnthropometry, Evolution, Physical Anthropology, Growth, Brain, Model, Humans, Allometry, Fossils, Animals, Method, Homo Sapiens, Biological evolution, Human Brain, Pan troglodytes, Time Factors, Hominidae, Body Weight, and Body Height
ABSTRACT Migliano has formulated and tested in her three publications (Migliano 2005; Walker et al. 2006; Migliano et al. 2007) a hypothesis explaining pygmy size as the result of a “fast” life history strategy (Charnov 1993) in which... more
ABSTRACT Migliano has formulated and tested in her three publications (Migliano 2005; Walker et al. 2006; Migliano et al. 2007) a hypothesis explaining pygmy size as the result of a “fast” life history strategy (Charnov 1993) in which early start of reproduction and growth termination are adaptive responses to high external mortality rates. We thank Becker et al. [2010 (this issue)] for the careful analysis of our work and the editors of Human Biology for the opportunity to clarify the points made in their commentary. Their criticisms are in part related to a regrettable typo in a figure that we did not see at the page proof stage; the other points do not seriously challenge our hypothesis, as discussed in what follows. The first criticism of Becker et al. (2010) is that we rely on a “threshold” size between pygmies and nonpygmies, which is at odds with life history theory, which postulates a continuous positive correlation between adult stature and mortality rates across populations. Becker and colleagues apparently are not aware that this is exactly the thesis originally proposed by Migliano (2005) in her dissertation and repeated in her two other publications (Migliano et al. 2007; Walker et al. 2006). Migliano’s hypothesis for pygmy size is an application of Charnov’s (1993) life history continuum across mammals to current human diversity, with pygmy groups and tall East African pastoralists occupying its fast and slow extremes. For example, Migliano (2005: 262) argues that “on one side, mortality and the chances of dying before reproducing select for earlier reproduction and consequently smaller body size; on the other, fitness increases with bigger body size, selecting for more time invested on growth and consequently later age at sexual maturation. The balance between these selective forces varies among different populations according to differences in mortality rates and according to how much the increase in body size adds to fertility.” To demonstrate the continuum, seven populations were originally analyzed. After reading Migliano (2005), Walker proposed to incorporate data from 15 other populations, and analyses successfully confirmed the proposed fast-slow continuum across humans (Walker et al. 2006). Migliano’s continuum hypothesis was proposed as a solution to a longstanding problem in anthropology: the evolution of the human pygmy phenotype. Until recently, the few answers were largely untested and were based on “special case” scenarios (forest vs. nonforest locomotion; hot vs. cold environment; undernourished vs. well-nourished populations; Diamond 1991). Our hypothesis postulates exactly the opposite view, using an established zoological theory (Charnov 1993) to explain human diversity. The claim that our results depend on an arbitrary categorization of humans into pygmies vs. nonpygmies is surprising: No single plot, table, or analysis in Migliano’s three publications requires a distinction between pygmy vs. nonpygmy groups. The second criticism by Becker et al. (2010) relates to our demographic data. Applying ecological models to humans is always a hard task, but we were as careful as possible with the data collection (started in 2002) and data analysis. Becker and colleagues argue that high mortality rates in the Batak, Agta, and Aeta reflect recent changes in lifestyles and therefore could not be associated with the evolution of their short stature. However, high mortality rates in these populations predate intensification of contact with neighboring populations. The Batak population has been declining for at least a century, not just since 1981 (Eder 1987). Mortality rates among the Agta did not significantly change following contact with farmers (Early and Headland 1998). Headland (1989: 65) showed that the main cause of adult mortality among the Agta was “sickness” (69% of males and 71% of females), most of which was of “unknown” origin during both foraging and peasant phases. Alcohol-related deaths accounted for only 2% of adult male deaths and 12% of female deaths. Finally, in the demographic analyses Migliano used data only from Aeta living in original villages with a seminomadic lifestyle. We also disagree that African pygmies are a better example of original lifestyle and mortality schedules than Asian pygmies. African pygmy groups have undergone population bottlenecks, with East African pygmies decreasing by up to 95% between 250 and 2,500 years ago; they have been in contact with farmers, leading to...
Research Interests: Genetics, Demography, Human Evolution, Anthropometry, Philippines, and 15 moreFertility, Evolution and Human Behavior, Human Biology, Humans, Life, Animals, Biological evolution, Life history strategy, Human Life History, Asian Continental Ancestry Group, Adaptive Response, Body Height, Pygmies, Reference Values, and Mortality rate
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The comparative analysis of animal growth still awaits full integration into life-history studies, partially due to the difficulty of defining a comparable measure of growth rate across species. Using growth data from 50 primate species,... more
The comparative analysis of animal growth still awaits full integration into life-history studies, partially due to the difficulty of defining a comparable measure of growth rate across species. Using growth data from 50 primate species, we introduce a modified "general growth model" and a dimensionless growth rate coefficient β that controls for size scaling and phylogenetic effects in the distribution of growth rates. Our results contradict the prevailing idea that slow growth characterizes primates as a group: the observed range of β values shows that not all primates grow slowly, with galago species exhibiting growth rates similar or above the mammalian average, while other strepsirrhines and most New World monkeys show limited reduction in growth rates. Low growth rate characterizes apes and some papionines. Phylogenetic regressions reveal associations between β and life-history variables, providing tests for theories of primate growth evolution. We also show that primate slow growth is an exclusively postnatal phenomenon. Our study exemplifies how the dimensionless approach promotes the integration of growth rate data into comparative life-history analysis, and demonstrates its potential applicability to other cases of adaptive diversification of animal growth patterns.