Ostrich eggshell bead strontium isotopes reveal persistent macroscale social networking across late Quaternary southern Africa.

Hunter-gatherer exchange networks dampen subsistence and reproductive risks by building relationships of mutual support outside local groups that are underwritten by symbolic gift exchange. Hxaro, the system of delayed reciprocity between Ju/'hoãn individuals in southern Africa's Kalahari Desert, is the best-known such example and the basis for most analogies and models of hunter-gatherer exchange in prehistory. However, its antiquity, drivers, and development remain unclear, as they do for long-distance exchanges among African foragers more broadly. Here we show through strontium isotope analyses of ostrich eggshell beads from highland Lesotho, and associated strontium isoscape development, that such practices stretch back into the late Middle Stone Age. We argue that these exchange items originated beyond the macroband from groups occupying the more water-stressed subcontinental interior. Tracking the emergence and persistence of macroscale, transbiome social networks helps illuminate the evolution of social strategies needed to thrive in stochastic environments, strategies that in our case study show persistence over more than 33,000 y.

Mercury isotopic evidence for multiple mercury sources in coal from the Illinois basin.

Coal combustion is the largest source of anthropogenic mercury (Hg) emissions to the atmosphere and, thus, has vast environmental implications. Recent developments in Hg stable isotope geochemistry offer a new tool for tracing sources and chemical transformations of anthropogenic Hg in the environment. We present here the first isotopic study of mercury in organic and inorganic constituents of four Pennsylvanian-age coal seams in the Illinois Basin, one of the main coal-producing areas in the USA. We report mass dependent isotopic variations relative to the NIST 3133 standard as δ(202)Hg and mass independent fractionation as Δ(199)Hg and Δ(201)Hg values. The data for Illinois coals show a wide range of δ(202)Hg (-0.75 to -2.68‰), Δ(201)Hg (0.04 to -0.22‰), and Δ(199)Hg (0.02 to -0.23‰). In contrast, vein pyrite from two coal seams is isotopically unfractionated relative to NIST 3133. Collectively, these data suggest that isotopically distinct Hg sources contributed to the organic and inorganic fractions of Illinois coals. The Δ(201)Hg/ Δ(199)Hg ratio of Illinois coals is 1:1, consistent with isotopic fractionation by photochemical reduction of Hg(2+) prior to deposition in coal-forming environments. The isotopic composition of Hg in pyrite is more likely derived from hydrothermal fluids that precipitated reduced sulfur in Illinois coal seams. These results demonstrate, for the first time, the potential of Hg isotopes to discriminate between syngenetic (depositional) and epigenetic (hydrothermal) sources of Hg in coal. Our findings may be useful in distinguishing among various geological processes controlling the distribution of Hg in coal and monitoring the fractions of Hg in emissions associated with organic versus inorganic components of coal.

Biogenic carbonate mercury and marine temperature records reveal global influence of Late Cretaceous Deccan Traps.

The climate and environmental significance of the Deccan Traps large igneous province of west-central India has been the subject of debate in paleontological communities. Nearly one million years of semi-continuous Deccan eruptive activity spanned the Cretaceous-Paleogene boundary, which is renowned for the extinction of most dinosaur groups. Whereas the Chicxulub impactor is acknowledged as the principal cause of these extinctions, the Deccan Traps eruptions are believed to have contributed to extinction patterns and/or enhanced ecological pressures on biota during this interval of geologic time. We present the first coupled records of biogenic carbonate clumped isotope paleothermometry and mercury concentrations as measured from a broad geographic distribution of marine mollusk fossils. These fossils preserve evidence of simultaneous increases in coastal marine temperatures and mercury concentrations at a global scale, which appear attributable to volcanic CO2 and mercury emissions. These early findings warrant further investigation with additional records of combined Late Cretaceous temperatures and mercury concentrations of biogenic carbonate.

Chronic mercury exposure in Late Neolithic/Chalcolithic populations in Portugal from the cultural use of cinnabar.

Cinnabar is a natural mercury sulfide (HgS) mineral of volcanic or hydrothermal origin that is found worldwide. It has been mined prehistorically and historically in China, Japan, Europe, and the Americas to extract metallic mercury (Hg(0)) for use in metallurgy, as a medicinal, a preservative, and as a red pigment for body paint and ceramics. Processing cinnabar via combustion releases Hg(0) vapor that can be toxic if inhaled. Mercury from cinnabar can also be absorbed through the gut and skin, where it can accumulate in organs and bone. Here, we report moderate to high levels of total mercury (THg) in human bone from three Late Neolithic/Chalcolithic (5400-4100 B.P.) sites in southern Portugal that were likely caused by cultural use of cinnabar. We use light stable isotope and Hg stable isotope tracking to test three hypotheses on the origin of mercury in this prehistoric human bone. We traced Hg in two individuals to cinnabar deposits near Almadén, Spain, and conclude that use of this mineral likely caused mild to severe mercury poisoning in the prehistoric population. Our methods have applications to bioarchaeological investigations worldwide, and for tracking trade routes and mobility of prehistoric populations where cinnabar use is documented.