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  • 1
    Publication Date: 2022-10-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Gu, S., Liu, Z., Oppo, D. W., Lynch-Stieglitz, J., Jahn, A., Zhang, J., & Wu, L. Assessing the potential capability of reconstructing glacial Atlantic water masses and AMOC using multiple proxies in CESM. Earth and Planetary Science Letters, 541, (2020): 11629, doi:10.1016/j.epsl.2020.116294.
    Description: Reconstructing the Atlantic Meridional Overturning Circulation (AMOC) during the Last Glacial Maximum (LGM) is essential for understanding glacial-interglacial climate change and the carbon cycle. However, despite many previous studies, uncertainties remain regarding the glacial water mass distributions in the Atlantic and the AMOC intensity. Here we use an isotope enabled ocean model with multiple geotracers (δ 13 C,E Νd,231 Pa/ 230Th,δ 18 Ο and Δ 14 C) and idealized water tracers to study the potential constraints on LGM ocean circulation from multiple proxies. Our model suggests that the glacial Atlantic water mass distribution can be accurately constrained by the air-sea gas exchange signature of water masses (δ13 C AS), but E Nd might overestimate the North Atlantic Deep Water (NADW) percentage in the deep Atlantic probably because of the boundary source of Nd. A sensitivity experiment with an AMOC of similar geometry but much weaker strength suggests that the correct AMOC geometry is more important than the AMOC strength for simulating the observed glacial δ13 C AS and E Nd and distributions. The kinematic tracer 231Pa/230Th is sensitive to AMOC intensity, but the interpretation might be complicated by the AMOC geometry and AABW transport changes during the LGM. δ 18 Ο in the benthic foraminifera (δ 18 Οc) from the Florida Straits provides a consistent measure of the upper ocean boundary current in the model, which potentially provides an unambiguous method to reconstruct glacial AMOC intensity. Finally, we propose that the moderate difference between AMOC intensity at LGM and PD, if any, is caused by the competition of the responses to CO2 forcing and continental ice sheet forcing.
    Description: We thank two anonymous reviewers for their useful and constructive comments. We also thank Editor Dr Laura F. Robinson for handling the manuscript. This work is supported by National Science Foundation of China No. 41630527, US National Science Foundation (NSF) P2C2 projects (1401778, 1401802, and 1566432). We would like to acknowledge the high-performance computing support from Yellowstone (ark:/85065/d7wd3xhc) and Cheyenne (doi:10.5065/D6RX99HX) provided by NCAR's Computational and Information Systems Laboratory, sponsored by the National Science Foundation and from Center for High Performance Computing and System Simulation, Pilot National Laboratory for Marine Science and Technology (Qingdao). Data used to produce the results in this study can be obtained from HPSS at CISL: /home/sgu28/CTRACE_decadal or by contacting the authors.
    Keywords: Last Glacial Maximum ; AMOC ; Water mass ; Multi-proxy
    Repository Name: Woods Hole Open Access Server
    Type: Article
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  • 2
    Publication Date: 2022-10-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Marty, B., Almayrac, M., Barry, P. H., Bekaert, D., V., Broadley, M. W., Byrne, D. J., Ballentine, C. J., & Caracausi, A. An evaluation of the C/N ratio of the mantle from natural CO2-rich gas analysis: Geochemical and cosmochemical implications. Earth and Planetary Science Letters, 551, (2020): 116574, doi:10.1016/j.epsl.2020.116574.
    Description: The terrestrial carbon to nitrogen ratio is a key geochemical parameter that can provide information on the nature of Earth's precursors, accretion/differentiation processes of our planet, as well as on the volatile budget of Earth. In principle, this ratio can be determined from the analysis of volatile elements trapped in mantle-derived rocks like mid-ocean ridge basalts (MORB), corrected for fractional degassing during eruption. However, this correction is critical and previous attempts have adopted different approaches which led to contrasting C/N estimates for the bulk silicate Earth (BSE) (Marty and Zimmermann, 1999; Bergin et al., 2015). Here we consider the analysis of CO2-rich gases worldwide for which a mantle origin has been determined using noble gas isotopes in order to evaluate the C/N ratio of the mantle source regions. These gases experienced little fractionation due to degassing, as indicated by radiogenic 4He / 40Ar* values (where 4He and 40Ar* are produced by the decay of U+Th, and 40K isotopes, respectively) close to the mantle production/accumulation values. The C/N and C/3 He ratios of gases investigated here are within the range of values previously observed in oceanic basalts. They point to an elevated mantle C/N ratio (∼350-470, molar) higher than those of potential cosmochemical accretionary endmembers. For example, the BSE C/N and 36 Ar / N ratios (160-220 and 75 x 10-7, respectively) are higher than those of CM-CI chondrites but within the range of CV-CO groups. This similarity suggests that the Earth accreted from evolved planetary precursors depleted in volatile and moderately volatile elements. Hence the high C / N composition of the BSE may be an inherited feature rather than the result of terrestrial differentiation. The C / N and 36 Ar / N ratios of the surface (atmosphere plus crust) and of the mantle cannot be easily linked to any known chondritic composition. However, these compositions are consistent with early sequestration of carbon into the mantle (but not N and noble gases), permitting the establishment of clement temperatures at the surface of our planet.
    Description: M.A, D.V.B, M.W.B, D.J.B and B.M were supported by the European Research Council (PHOTONIS project, grant agreement No. 695618 to B.M.). Samples were collected as part of Study # YELL-08056 - Xenon anomalies in the Yellowstone Hotspot. We would like to thank Annie Carlson and all of the rangers at the Yellowstone National Park for providing invaluable advice and help when collecting the samples. This work was partially supported by a grant (G-2016-7206) from the Alfred P. Sloan Foundation and the Deep Carbon Observatory to P.H.B as well as NSF award 2015789 to P.H.B.. Sampling at Mt. Etna and gas analysis was supported by Instituto Nazionale di Geofisica e Vulcanologia Palermo. Fruitful discussions with Marc Hirschmann helped us to shape the ideas presented in this work. We acknowledge detailed and insightful reviews by Sami Mikhail and an anonymous reviewer, and efficient editing by Frederic Moynier. This is CRPG contribution 2741.
    Keywords: Carbon ; Nitrogen ; Earth ; Mantle ; Gases
    Repository Name: Woods Hole Open Access Server
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  • 3
    Publication Date: 2022-05-26
    Description: © The Author(s), 2020. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Eugster, W., Laundre, J., Eugster, J., & Kling, G. W. Long-term reliability of the figaro TGS 2600 solid-state methane sensor under low-Arctic conditions at Toolik Lake, Alaska. Atmospheric Measurement Techniques, 13(5), (2020): 2681-2695, doi:10.5194/amt-13-2681-2020.
    Description: The TGS 2600 was the first low-cost solid-state sensor that shows a response to ambient levels of CH4 (e.g., range ≈1.8–2.7 µmol mol−1). Here we present an empirical function to correct the TGS 2600 signal for temperature and (absolute) humidity effects and address the long-term reliability of two identical sensors deployed from 2012 to 2018. We assess the performance of the sensors at 30 min resolution and aggregated to weekly medians. Over the entire period the agreement between TGS-derived and reference CH4 mole fractions measured by a high-precision Los Gatos Research instrument was R2=0.42, with better results during summer (R2=0.65 in summer 2012). Using absolute instead of relative humidity for the correction of the TGS 2600 sensor signals reduced the typical deviation from the reference to less than ±0.1 µmol mol−1 over the full range of temperatures from −41 to 27 ∘C. At weekly resolution the two sensors showed a downward drift of signal voltages indicating that after 10–13 years a TGS 2600 may have reached its end of life. While the true trend in CH4 mole fractions measured by the high-quality reference instrument was 10.1 nmolmol−1yr−1 (2012–2018), part of the downward trend in sensor signal (ca. 40 %–60 %) may be due to the increase in CH4 mole fraction because the sensor voltage decreases with increasing CH4 mole fraction. Weekly median diel cycles tend to agree surprisingly well between the TGS 2600 and reference measurements during the snow-free season, but in winter the agreement is lower. We suggest developing separate functions for deducing CH4 mole fractions from TGS 2600 measurements under cold and warm conditions. We conclude that the TGS 2600 sensor can provide data of research-grade quality if it is adequately calibrated and placed in a suitable environment where cross-sensitivities to gases other than CH4 are of no concern.
    Description: We acknowledge support received from Arctic LTER grants (grant nos. NSF-DEB-1637459, 1026843, 1754835, and NSF-PLR 1504006) and supplemental funding from the NSF-NEON and OPP-AON programs. Gaius R. Shaver (MBL) is acknowledged for initiating the study and supporting our activities in all aspects. ETH is acknowledge for supporting the purchase of the Fast Greenhouse Gas Analyzer that replaced the older Fast Methane Analyzer in 2016 (grant no. 0-43683-11).
    Repository Name: Woods Hole Open Access Server
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  • 4
    Publication Date: 2022-01-07
    Description: Atmospheric deposition of aerosols to the ocean provides an important pathway for the supply of vital micronutrients, including trace metals. These trace metals are essential for phytoplankton growth, and therefore their delivery to marine ecosystems can strongly influence the ocean carbon cycle. The solubility of trace metals in aerosols is a key parameter to better constrain their potential impact on phytoplankton growth. To date, a wide range of experimental approaches and nomenclature have been used to define aerosol trace metal solubility, making data comparison between studies difficult. Here we investigate and discuss several laboratory leaching protocols to determine the solubility of key trace metals in aerosol samples, namely iron, cobalt, manganese, copper, lead, vanadium, titanium and aluminium. Commonly used techniques and tools are also considered such as enrichment factor calculations and air mass back-trajectory projections and recommendations are given for aerosol field sampling, laboratory processing (including leaching and digestion) and analytical measurements. Finally, a simple 3-step leaching protocol combining commonly used protocols is proposed to operationally define trace metal solubility in aerosols. The need for standard guidelines and protocols to study the biogeochemical impact of atmospheric trace metal deposition to the ocean has been increasingly emphasised by both the atmospheric and oceanographic communities. This lack of standardisation currently limits our understanding and ability to predict ocean and climate interactions under changing environmental conditions.
    Type: Article , PeerReviewed
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