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Radiocarbon dating is arguably the most common method for dating Quaternary deposits. However, accurate age assignments using radiocarbon dating are dependent on knowing the radiocarbon reservoir. For the coastal waters across Antarctica, the radiocarbon reservoirs show significant variation, ranging from 700 to 6000 years depending on the material dated and the period in question. In this study, we examine the radiocarbon reservoir age for the shallow waters of the Southern Ocean using 23 whale bones salvaged from commercial whaling operations on or near the Western Antarctic Peninsula between 1904 and 1916. The species origin of the bones had been identified previously as humpback, fin, or blue whales using sequences of mitochondrial (mt)DNA. We find an average reservoir age of 1050 ± 135 years for these 23 whale bones, with a <100-year difference in the reservoir age by species. A comparison between our results and other studies through the Holocene suggest that the Southern Ocean surface water radiocarbon reservoir age is of a similar magnitude across much of Antarctica and has not significantly changed for the last 14,000 years. Combining our new ages with existing data sets provides insight to the stability of the Southern Ocean marine radiocarbon reservoir age, enhancing our understanding of ocean ventilation and upwelling dynamics throughout the Holocene. 

This releaser corresponds to publication of the manuscript 

The observation of extremely low radiocarbon content / old radiocarbon ages (>4000 years old) in the intermediate-depth ocean during the last ice age draws attention to our incomplete understanding of ocean carbon cycling. For example, glacial-interglacial seawater 14C anomalies near the Gulf of California have been explained by both the advection from a 14C-depleted abyssal source and local geologic carbon flux. To provide insight to this the origin of the seawater 14C anomalies, we have produced several new records of glacial-interglacial intermediate water (i.e., 14C, δ11B, δ18O, and δ13C) in waters that are “upstream” and “downstream” of the Gulf of California. These observations plus geochemical modeling allow us to: (1) Answer whether the old seawater 14C ages are advected or produced locally; (2) Identify the approximate chemical make-up of this carbon; and (3) Consider the role of known sedimentary processes in this carbon flux to the ocean. (Note that several sites have age model controls based on terrestrial plant 14C ages, providing more confidence in our results.) Our new measurements and modeling indicate that the well-established >4000-year-old seawater 14C anomalies observed near known seafloor volcanism in the Gulf of California are not present “upstream,” indicating that this carbon flux results from a “local” geologic carbon. Furthermore, based on our new benthic foraminifera δ11B measurements, this local carbon Blux does not appear to affect seawater pH. Finally, we suggest several potential geologic carbon source(s) that could explain the anomalously old seawater 14C ages, the relatively unremarkable changes in seawater δ13C, and the essentially negligible change in seawater pH. 

Large carnivores (order Carnivora) are among the world's most threatened mammals due to a confluence of ecological and social forces that have unfolded over centuries. Combining specimens from natural history collections with documents from archival records, we reconstructed the factors surrounding the extinction of the California grizzly bear (Ursus arctos californicus), a once-abundant brown bear subspecies last seen in 1924. Historical documents portrayed California grizzlies as massive hypercarnivores that endangered public safety. Yet, morphological measurements on skulls and teeth generate smaller body size estimates in alignment with extant North American grizzly populations (approx. 200 kg). Stable isotope analysis (δ¹³C,δ¹⁵N) of pelts and bones (n= 57) revealed that grizzlies derived less than 10% of their nutrition from terrestrial animal sources and were therefore largely herbivorous for millennia prior to the first European arrival in this region in 1542. Later colonial land uses, beginning in 1769 with the Mission era, led grizzlies to moderately increase animal protein consumption (up to 26% of diet), but grizzlies still consumed far less livestock than otherwise claimed by contemporary accounts. We show how human activities can provoke short-term behavioural shifts, such as heightened levels of carnivory, that in turn can lead to exaggerated predation narratives and incentivize persecution, triggering rapid loss of an otherwise widespread and ecologically flexible animal. 

The 14-carbon in animal tissues records the time that the tissues are formed; since the 1960s, using the “bomb curve” for 14 C, the age of animal death can be determined accurately. Using animal tissue samples of known collection and formation dates for calibration, we determine the age of ivory samples from four ivory seizures made by law enforcement agencies between 2017 and 2019. The 14 C measurements from these seizures show that most ivory in the illegal wildlife trade is from animals from recent poaching activities. However, one seizure has a large fraction of ivory that is more than 30 y old, consistent with markings on the tusks indicating they were derived from a government stockpile. 

Abstract. Most extant ice caps mantling low-relief Arctic Canada landscapes remained cold based throughout the late Holocene, preserving in situ bryophytes killed as ice expanded across vegetated landscapes. After reaching peak late Holocene dimensions ∼1900 CE, ice caps receded as Arctic summers warmed, exposing entombed vegetation. The calibrated radiocarbon ages of entombed moss collected near ice cap margins (kill dates) define when ice advanced across the site, killing the moss, and remained over the site until the year of their collection. In an earlier study, we reported 94 last millennium radiocarbon dates on in situ dead moss collected at ice cap margins across Baffin Island, Arctic Canada. Tight clustering of those ages indicated an abrupt onset of the Little Ice Age at ∼1240 CE and further expansion at ∼1480 CE coincident with episodes of major explosive volcanism. Here we test the confidence in kill dates as reliable predictors of expanding ice caps by resampling two previously densely sampled ice complexes ∼15 years later after ∼250 m of ice recession. The probability density functions (PDFs) of the more recent series of ages match PDFs of the earlier series but with a larger fraction of early Common Era ages. Post 2005 CE ice recession has exposed relict ice caps that grew during earlier Common Era advances and were preserved beneath later ice cap growth. We compare the 106 kill dates from the two ice complexes with 80 kill dates from 62 other ice caps within 250 km of the two densely sampled ice complexes. The PDFs of kill dates from the 62 other ice caps cluster in the same time windows as those from the two ice complexes alone, with the PDF of all 186 kill dates documenting episodes of widespread ice expansion restricted almost exclusively to 250–450 CE, 850–1000 CE, and a dense early Little Ice Age cluster with peaks at ∼1240 and ∼1480 CE. Ice continued to expand after 1480 CE, reaching maximum dimensions at ∼1880 CE that are still visible as zones of sparse vegetation cover in remotely sensed imagery. Intervals of widespread ice cap expansion coincide with persistent decreases in mean summer surface air temperature for the region in a Community Earth System Model (CESM) fully coupled Common Era simulation, suggesting the primary forcings of the observed snowline lowering were both modest declines in summer insolation and cooling resulting from explosive volcanism, most likely intensified by positive feedbacks from increased snow cover and sea ice and reduced northward heat transport by the oceans. The clusters of ice cap expansion defined by moss kill dates are mirrored in an annually resolved Common Era record of ice cap dimensions in Iceland, suggesting this is a circum-North-Atlantic–Arctic climate signal for the Common Era. During the coldest century of the Common Era, 1780–1880 CE, ice caps mantled >11 000 km2 of north-central Baffin Island, whereas <100 km2 is glaciated at present. The peak Little Ice Age state approached conditions expected during the inception phase of an ice age and was only reversed after 1880 CE by anthropogenic alterations of the planetary energy balance. 

The cause, or causes, of the Pleistocene megafaunal extinctions have been difficult to establish, in part because poor spatiotemporal resolution in the fossil record hinders alignment of species disappearances with archeological and environmental data. We obtained 172 new radiocarbon dates on megafauna from Rancho La Brea in California spanning 15.6 to 10.0 thousand calendar years before present (ka). Seven species of extinct megafauna disappeared by 12.9 ka, before the onset of the Younger Dryas. Comparison with high-resolution regional datasets revealed that these disappearances coincided with an ecological state shift that followed aridification and vegetation changes during the Bølling-Allerød (14.69 to 12.89 ka). Time-series modeling implicates large-scale fires as the primary cause of the extirpations, and the catalyst of this state shift may have been mounting human impacts in a drying, warming, and increasingly fire-prone ecosystem.