| Literature DB >> 33397930 |
Lucas C R Silva1,2, Rodrigo Studart Corrêa3, Jamie L Wright4, Barbara Bomfim4,5, Lauren Hendricks6, Daniel G Gavin6, Aleksander Westphal Muniz7, Gilvan Coimbra Martins7, Antônio Carlos Vargas Motta8, Julierme Zimmer Barbosa9, Vander de Freitas Melo8, Scott D Young10, Martin R Broadley10, Roberto Ventura Santos11.
Abstract
Amazonian Dark Earths (ADEs) are unusually fertile soils characterised by elevated concentrations of microscopic charcoal particles, which confer their distinctive colouration. Frequent occurrences of pre-Columbian artefacts at ADE sites led to their ubiquitous classification as Anthrosols (soils of anthropic origin). However, it remains unclear how indigenous peoples created areas of high fertility in one of the most nutrient-impoverished environments on Earth. Here, we report new data from a well-studied ADE site in the Brazilian Amazon, which compel us to reconsider its anthropic origin. The amounts of phosphorus and calcium-two of the least abundant macronutrients in the region-are orders of magnitude higher in ADE profiles than in the surrounding soil. The elevated levels of phosphorus and calcium, which are often interpreted as evidence of human activity at other sites, correlate spatially with trace elements that indicate exogenous mineral sources rather than in situ deposition. Stable isotope ratios of neodymium, strontium, and radiocarbon activity of microcharcoal particles also indicate exogenous inputs from alluvial deposition of carbon and mineral elements to ADE profiles, beginning several thousands of years before the earliest evidence of soil management for plant cultivation in the region. Our data suggest that indigenous peoples harnessed natural processes of landscape formation, which led to the unique properties of ADEs, but were not responsible for their genesis. If corroborated elsewhere, this hypothesis would transform our understanding of human influence in Amazonia, opening new frontiers for the sustainable use of tropical landscapes going forward.Entities:
Year: 2021 PMID: 33397930 PMCID: PMC7782733 DOI: 10.1038/s41467-020-20184-2
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919