2015
DOI: 10.1007/s10816-014-9237-4
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Demography and the Palaeolithic Archaeological Record

Abstract: Demographic change has recently re-emerged as a key explanation for socio-cultural changes documented in the prehistoric archaeological record. While the majority of studies of Pleistocene demography have been conducted by geneticists, the archaeological records of the Palaeolithic should not be ignored as a source of data on past population trends. This paper forms both a comprehensive synthesis and the first critical review of current archaeological research into Palaeolithic demography. Within prevailing ar… Show more

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Cited by 66 publications
(58 citation statements)
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References 364 publications
(407 reference statements)
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“…As for the density estimates, however, a few more words of caution must be inserted here: the remarkable feat (Mazet et al, 2016) of the Li and Durbin landmark study in 2011 (Li & Durbin, 2011), rests on several assumptions that may be questionable, especially in the case of Pleistocene populations of humans at extremely low densities: panmixia, or the spread in a two-dimensional diffusion process, and a comparison of data sets obtained with different methods under varying assumptions from very different populations, even from different species (e.g., Lorenzen et al, 2011). However, the extremely small human population size estimates for Pleistocene Eurasia, as calculated by the "genetic" Ne, and here used as substitute for Nc -the census population size -are well supported by recent estimates based on the archeological evidence from Pleistocene camp sites in Europe (French, 2015;French & Collins, 2015;Maier et al, 2016). The human population, in sharp contrast, numbering all over Eurasia only a few thousand individuals, narrowly had escaped extinction during the Pleistocene bottleneck, remained on a level of ecological insignificance for thousands of years, and started its rise only after the LGM to become the ultimate keystone species and "natural catastrophe" (Schaller, 1991).…”
Section: Humans and Fauna In The Southern Fringes Of The Mammoth Steppesupporting
confidence: 53%
“…As for the density estimates, however, a few more words of caution must be inserted here: the remarkable feat (Mazet et al, 2016) of the Li and Durbin landmark study in 2011 (Li & Durbin, 2011), rests on several assumptions that may be questionable, especially in the case of Pleistocene populations of humans at extremely low densities: panmixia, or the spread in a two-dimensional diffusion process, and a comparison of data sets obtained with different methods under varying assumptions from very different populations, even from different species (e.g., Lorenzen et al, 2011). However, the extremely small human population size estimates for Pleistocene Eurasia, as calculated by the "genetic" Ne, and here used as substitute for Nc -the census population size -are well supported by recent estimates based on the archeological evidence from Pleistocene camp sites in Europe (French, 2015;French & Collins, 2015;Maier et al, 2016). The human population, in sharp contrast, numbering all over Eurasia only a few thousand individuals, narrowly had escaped extinction during the Pleistocene bottleneck, remained on a level of ecological insignificance for thousands of years, and started its rise only after the LGM to become the ultimate keystone species and "natural catastrophe" (Schaller, 1991).…”
Section: Humans and Fauna In The Southern Fringes Of The Mammoth Steppesupporting
confidence: 53%
“…These studies have been repeatedly cited by Palaeolithic archaeologists as evidence that population size affects cultural change [8,16]. In this section, we will show that this is not correct.…”
Section: The Mechanics Of the Population Size Hypothesismentioning
confidence: 81%
“…Inferences of Palaeolithic demography from archaeological proxies usually rely on changes in (i) the number of sites in a region for a given time interval, (ii) artefact accumulation rates, (iii) site size or (iv) diet, particularly increased dietary breadth, the inclusion of lower ranked resources, intensified predation pressure and prey extirpation [36]. For East Africa, Blome et al [35] report increases in site frequency beginning approximately 90 ka, but temporally and spatially limited excavations and the rarity of preserved or reported fauna currently severely limit use of analyses of site size or changes in dietary breadth [3,35].…”
Section: Demography Mobility and Technological Organizationmentioning
confidence: 99%
“…the density and predictability of key resources), and the proximity and number of other human groups, as a more densely packed landscape reduces mobility options [41]. While an individual forager or group may shift residential mobility seasonally or over longer time periods [41], data from recent and historic foragers [36,37,[41][42][43][44][45][46] suggest that residential mobility is inversely correlated with net primary productivity and the abundance and predictability of key resources. When resources are abundant and predictable, there is little need for a group to incur the energetic costs of high residential mobility, but when sparse, the costs of mobility are outweighed by the increase in returns gained from exploiting the broader landscape.…”
Section: (A) Measuring Residential Mobility From Lithic Datamentioning
confidence: 99%