Dozens of large mammals such as mammoth and mastodon disappeared in North America at the end of the Pleistocene with climate change and “overkill” by human hunters the most widely-argued causes. However, the population dynamics of humans and megafauna preceding extinctions have received little attention even though such information may be telling as we expect increasing human populations to be correlated with megafaunal declines if hunting caused extinctions. No such trends are expected if climate change was the primary cause. We present tests of these hypotheses here by using summed calibrated radiocarbon date distributions to reconstruct population levels of megafauna and humans. The results suggest that the causes for extinctions varied across taxa and by region. In three cases, extinctions appear linked to hunting, while in five others they are consistent with the ecological effects of climate change and in a final case, both hunting and climate change appear responsible.
The transition to agriculture is one of the most significant events in human prehistory; yet, explaining why people initially domesticated plants and animals remains a contentious research problem in archaeology. Two competing hypotheses dominate current debates. The first draws on niche construction theory to emphasize how intentional management of wild resources should lead to domestication regardless of Malthusian population–resource imbalances. The second relies on models from behavioural ecology (BE) to highlight how individuals should only exert selective pressure on wild resources during times of population–resource imbalance. We examine these hypotheses to explain the domestication event which occurred in Eastern North America approximately 5000 years ago. Using radiocarbon date density and site counts as proxies for human population, we find that populations increased significantly in the 1000 years prior to initial domestication. We therefore suggest that high populations prior to 5000 cal BP may have experienced competition for and possibly overexploitation of resources, altering the selective pressures on wild plants thereby producing domesticates. These findings support the BE hypothesis of domestication occurring in the context of population–resource imbalances. Such deficits, driven either by increased populations or decreased resource abundance, are predicted to characterize domestication events elsewhere.
Historical ecology has revolutionized our understanding of fisheries and cultural landscapes, demonstrating the value of historical data for evaluating the past, present, and future of Earth’s ecosystems. Despite several important studies, Indigenous fisheries generally receive less attention from scholars and managers than the 17th–20th century capitalist commercial fisheries that decimated many keystone species, including oysters. We investigate Indigenous oyster harvest through time in North America and Australia, placing these data in the context of sea level histories and historical catch records. Indigenous oyster fisheries were pervasive across space and through time, persisting for 5000–10,000 years or more. Oysters were likely managed and sometimes “farmed,” and are woven into broader cultural, ritual, and social traditions. Effective stewardship of oyster reefs and other marine fisheries around the world must center Indigenous histories and include Indigenous community members to co-develop more inclusive, just, and successful strategies for restoration, harvest, and management.
Human populations distribute themselves across landscapes in clearly patterned ways, but accurate and theoretically informed predictions and explanations of that patterning in the archaeological record can prove difficult. Recently, archaeologists have begun applying a unifying theoretical framework derived from population and behavioural ecology to understand human population distribution and movement: the ideal distribution model (IDM). The three variants of this IDM-the ideal free distribution, the ideal free distribution with an Allee effect, and the ideal despotic distribution-are capable of generating testable hypotheses concerning the colonisation of landscapes, the spatial distribution of populations, cooperation and competition, social hierarchy and inequality, and the impacts of subsistence on settlement patterns. Their success in addressing such wide-ranging research questions demonstrates that IDMs are not only helpful for analysing settlement patterns in relation to environmental factors, but for better understanding the social forces that impact population distribution, as well. There seem to be no geographic or temporal bounds to the utility of IDMs, and we look forward to the application of these models in ever more diverse settings.
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