21 research outputs found

    Erroneously old radiocarbon ages from terrestrial pollen concentrates in Yellowstone Lake, Wyoming, USA

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    © The Author(s), 2021. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in [Schiller, C. M., Whitlock, C., Elder, K. L., Iverson, N. A., & Abbott, M. B. Erroneously old radiocarbon ages from terrestrial pollen concentrates in Yellowstone Lake, Wyoming, USA. Radiocarbon, 63(1), (2021): 321-342, https://doi.org/10.1017/RDC.2020.118.Accelerator mass spectrometry (AMS) dating of pollen concentrates is often used in lake sediment records where large, terrestrial plant remains are unavailable. Ages produced from chemically concentrated pollen as well as manually picked Pinaceae grains in Yellowstone Lake (Wyoming) sediments were consistently 1700–4300 cal years older than ages established by terrestrial plant remains, tephrochronology, and the age of the sediment-water interface. Previous studies have successfully utilized the same laboratory space and methods, suggesting the source of old-carbon contamination is specific to these samples. Manually picking pollen grains precludes admixture of non-pollen materials. Furthermore, no clear source of old pollen grains occurs on the deglaciated landscape, making reworking of old pollen grains unlikely. High volumes of CO2 are degassed in the Yellowstone Caldera, potentially introducing old carbon to pollen. While uptake of old CO2 through photosynthesis is minor (F14C approximately 0.99), old-carbon contamination may still take place in the water column or in surficial lake sediments. It remains unclear, however, what mechanism allows for the erroneous ages of highly refractory pollen grains while terrestrial plant remains were unaffected. In the absence of a satisfactory explanation for erroneously old radiocarbon ages from pollen concentrates, we propose steps for further study.This research was supported by NSF Grant No. 1515353 to C. Whitlock and sampling in Yellowstone National Park was conducted under permits YELL-SCI-0009 and YELL-SCI-5054

    Volcanic glass from the 1.8 ka Taupƍ eruption (New Zealand) detected in Antarctic ice at ~ 230 CE.

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    Chemical anomalies in polar ice core records are frequently linked to volcanism; however, without the presence of (crypto)tephra particles, links to specific eruptions remain speculative. Correlating tephras yields estimates of eruption timing and potential source volcano, offers refinement of ice core chronologies, and provides insights into volcanic impacts. Here, we report on sparse rhyolitic glass shards detected in the Roosevelt Island Climate Evolution (RICE) ice core (West Antarctica), attributed to the 1.8 ka Taupƍ eruption (New Zealand)-one of the largest and most energetic Holocene eruptions globally. Six shards of a distinctive geochemical composition, identical within analytical uncertainties to proximal Taupƍ glass, are accompanied by a single shard indistinguishable from glass of the ~25.5 ka ƌruanui supereruption, also from Taupƍ volcano. This double fingerprint uniquely identifies the source volcano and helps link the shards to the climactic phase of the Taupƍ eruption. The englacial Taupƍ-derived glass shards coincide with a particle spike and conductivity anomaly at 278.84 m core depth, along with trachytic glass from a local Antarctic eruption of Mt. Melbourne. The assessed age of the sampled ice is 230 ± 19 CE (95% confidence), confirming that the published radiocarbon wiggle-match date of 232 ± 10 CE (2 SD) for the Taupƍ eruption is robust

    The WAIS Divide deep ice core WD2014 chronology - Part 2: Annual-layer counting (0-31 ka BP)

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    International audienceWe present the WD2014 chronology for the upper part (0–2850 m; 31.2 ka BP) of the West Antarctic Ice Sheet (WAIS) Divide (WD) ice core. The chronology is based on counting of annual layers observed in the chemical, dust and electrical conductivity records. These layers are caused by seasonal changes in the source, transport, and deposi-tion of aerosols. The measurements were interpreted manually and with the aid of two automated methods. We validated the chronology by comparing to two high-accuracy, absolutely dated chronologies. For the Holocene, the cos-mogenic isotope records of 10 Be from WAIS Divide and 14 C for IntCal13 demonstrated that WD2014 was consistently accurate to better than 0.5 % of the age. For the glacial period, comparisons to the Hulu Cave chronology demonstrated that WD2014 had an accuracy of better than 1 % of the age at three abrupt climate change events between 27 and 31 ka. WD2014 has consistently younger ages than Green-land ice core chronologies during most of the Holocene. For Published by Copernicus Publications on behalf of the European Geosciences Union. 770 M. Sigl et al.: The WAIS Divide deep ice core WD2014 chronology the Younger Dryas–Preboreal transition (11.595 ka; 24 years younger) and the Bþlling–Allerþd Warming (14.621 ka; 7 years younger), WD2014 ages are within the combined uncertainties of the timescales. Given its high accuracy, WD2014 can become a reference chronology for the Southern Hemisphere, with synchronization to other chronologies feasible using high-quality proxies of volcanism, solar activity , atmospheric mineral dust, and atmospheric methane concentrations

    Synchronous volcanic eruptions and abrupt climate change ∌17.7 ka plausibly linked by stratospheric ozone depletion.

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    Glacial-state greenhouse gas concentrations and Southern Hemisphere climate conditions persisted until ∌17.7 ka, when a nearly synchronous acceleration in deglaciation was recorded in paleoclimate proxies in large parts of the Southern Hemisphere, with many changes ascribed to a sudden poleward shift in the Southern Hemisphere westerlies and subsequent climate impacts. We used high-resolution chemical measurements in the West Antarctic Ice Sheet Divide, Byrd, and other ice cores to document a unique, ∌192-y series of halogen-rich volcanic eruptions exactly at the start of accelerated deglaciation, with tephra identifying the nearby Mount Takahe volcano as the source. Extensive fallout from these massive eruptions has been found >2,800 km from Mount Takahe. Sulfur isotope anomalies and marked decreases in ice core bromine consistent with increased surface UV radiation indicate that the eruptions led to stratospheric ozone depletion. Rather than a highly improbable coincidence, circulation and climate changes extending from the Antarctic Peninsula to the subtropics-similar to those associated with modern stratospheric ozone depletion over Antarctica-plausibly link the Mount Takahe eruptions to the onset of accelerated Southern Hemisphere deglaciation ∌17.7 ka

    New Zealand supereruption provides time marker for the Last Glacial Maximum in Antarctica

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    Multiple, independent time markers are essential to correlate sediment and ice cores from the terrestrial, marine and glacial realms. These records constrain global paleoclimate reconstructions and inform future climate change scenarios. In the Northern Hemisphere, sub-visible layers of volcanic ash (cryptotephra) are valuable time markers due to their widespread dispersal and unique geochemical fingerprints. However, cryptotephra are not as widely identified in the Southern Hemisphere, leaving a gap in the climate record, particularly during the Last Glacial Maximum (LGM). Here we report the first identification of New Zealand volcanic ash in Antarctic ice. The Oruanui supereruption from Taupo volcano (25,580 ± 258 cal. a BP) provides a key time marker for the LGM in the New Zealand sector of the SW Pacific. This finding provides a high-precision chronological link to mid-latitude terrestrial and marine sites, and sheds light on the long-distance transport of tephra in the Southern Hemisphere. As occurred after identification of the Alaskan White River Ash in northern Europe, recognition of ash from the Oruanui eruption in Antarctica dramatically increases the reach and value of tephrochronology, providing links among climate records in widely different geographic areas and depositional environments

    The persistence of salt-affected paleosols at Gona, Ethiopia: A sedimentary archive of Middle to Late Pleistocene soil salinity within a corridor of early human migration

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    The origin of Homo sapiens and their subsequent dispersal out of Africa during the Mid-to-Late Pleistocene are hallmark events in the evolution of humans and are recorded as snapshots within terrestrial sedimentary deposits in East Africa. This study uses paleosols to reconstruct paleoenvironments of those events at Gona, Ethiopia - an area with one of the most continuous records of East African Paleolithic and Neolithic archaeology. A preliminary survey of Gona paleosols from the past 250,000 years shows a wide range of paleosol types that resemble modern-day Entisols, Inceptisols and Vertisols. Approximate paleosol ages were estimated using nearby OSL, 14 C, U-series, 40 Ar/ 39 Ar and volcanic glass chemistry. The pH and EC of these paleosols were measured as they are weakly compacted and show few signs of diagenesis. Mean pH values are slightly alkaline (7.8 ±0.63) and mean EC values (9.8 ±7.9) are saline, suggesting salt-affected soil development. The high standard deviation of EC results from low-EC sodic soils found in some units. These pH and EC findings are consistent with bulk geochemical-based pedotransfer functions on paleo-Vertisols, which indicate the presence of saline and sodic conditions. Much like modern-day tributary and trunk-channel floodplains, these paleosols likely hosted halophytes like Tamarix, Vachellia and salt-tolerant grasses, flora which are commonly found at present-day Gona. Notably, some late Pleistocene salt-affected paleosols that coincide with Marine Isotope Stage 5 and the African Humid Period show signs of prolonged soil saturation and nearby standing water. High evapotranspiration due to Gona’s semi-arid climate likely resulted in low infiltration and subsurface drainage of water, insufficient to transport salt out of the system, resulting in abundant saline soil formation at the site. The high salinity of Mid-to-Late Pleistocene Gona paleosols, likely due to source material, climate, and drainage, limits the use of many bulk geochemical proxies that were developed using mostly normal, non-saline soils. Despite this, the results of this study shed light on the climate and environment of our ancestors at the pedon scale
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