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Last glacial atmospheric CO2 decline due to widespread Pacific deep-water expansion

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Ocean circulation critically affects the global climate and atmospheric carbon dioxide through redistribution of heat and carbon in the Earth system. Despite intensive research, the nature of past ocean circulation changes remains elusive. Here we present deep-water carbonate ion concentration reconstructions for widely distributed locations in the Atlantic Ocean, where low carbonate ion concentrations indicate carbon-rich waters. These data show a low-carbonate-ion water mass that extended northward up to about 20° S in the South Atlantic at 3–4 km depth during the Last Glacial Maximum. In combination with radiocarbon ages, neodymium isotopes and carbon isotopes, we conclude that this low-carbonate-ion signal reflects a widespread expansion of carbon-rich Pacific deep waters into the South Atlantic, revealing a glacial deep Atlantic circulation scheme different than commonly considered. Comparison of high-resolution carbonate ion records from different water depths in the South Atlantic indicates that this Pacific deep-water expansion developed from approximately 38,000 to 28,000 years ago. We infer that its associated carbon sequestration may have contributed critically to the contemporaneous decline in atmospheric carbon dioxide, thereby helping to initiate the glacial maximum.
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https://doi.org/10.1038/s41561-020-0610-5
1Research School of Earth Sciences, The Australian National University, Canberra, Australian Capital Territory, Australia. 2State Key Laboratory of Loess
and Quaternary Geology, Institute of Earth Environment, Chinese Academy of Sciences, Xi’an, China. 3Climate Change Research Centre, University of
New South Wales, Sydney, New South Wales, Australia. 4CAS Center for Excellence in Quaternary Science and Global Change, Xi’an, China. 5Open Studio
for Oceanic–Continental Climate and Environment Changes, Qingdao National Laboratory for Marine Science and Technology, Qingdao, China.
6Lamont–Doherty Earth Observatory, Columbia University, New York, NY, USA. 7State Key Laboratory of Marine Geology, Tongji University, Shanghai,
China. 8Department of Earth Sciences, University of Cambridge, Cambridge, UK. 9Ocean and Earth Science, National Oceanography Centre, University
of Southampton, Southampton, UK. 10Centro de Investigación Mariña, GEOMA, Palaeoclimatology Lab, Universidade de Vigo, Vigo, Spain.
e-mail: jimin.yu@anu.edu.au
Ocean circulation and the carbon cycle are intricately linked,
thus ocean circulation reconstructions can provide impor-
tant insights into the mechanisms of past atmospheric CO2
changes. Circulation in the deep (more than ~2.5 km) Atlantic dur-
ing the Last Glacial Maximum (LGM; 18–22 thousand years ago
(ka)) is traditionally viewed as following a mixing model between
deep waters formed in the basin’s polar regions, without much con-
tribution from waters from other oceans14. Using this long-held
ocean circulation model, however, it is difficult to explain the
observed older radiocarbon (14C) ages and more radiogenic neo-
dymium isotopic (εNd) signatures at ~3.8 km than at ~5 km in the
LGM South Atlantic5,6 (Fig. 1). Burke etal.7 showed that sluggish
recirculation of southern-sourced waters combined with reduced
mixing with 14C-rich northern-sourced waters can contribute to old
14C ages at ~3.8 km, in the absence of interocean water-mass inter-
actions. Yet, additional mechanisms are probably needed to fully
explain the depth structure and large magnitude of 14C age changes,
along with the more radiogenic εNd signal observed at 3.8 km
(Fig. 1). Pacific Deep Water (PDW) can notably affect deglacial εNd
signatures in the Drake Passage (Southern Ocean)8, but their role in
the deep South Atlantic during the LGM remains unexplored. PDW
stores a large amount of respired carbon9,10, thus temporal changes
in its volumetric extent would have important implications for past
atmospheric CO2 levels.
Deep-water carbonate ion concentrations ([CO32–]) can provide
critical information about past deep ocean circulation and dissolved
inorganic carbon (DIC) changes. In the modern Atlantic, contrast-
ing [CO32–] signatures between water masses reflect ocean circula-
tion patterns11 (Fig. 2). Also, past DIC changes may be quantified
from [CO32–] reconstructions12. Here we present deep-water [CO32–]
reconstructions for extensive locations in the Atlantic to deci-
pher the role of ocean circulation in the glacial atmospheric CO2
decrease. We focus on deep South Atlantic hydrography, which
remains incompletely understood despite intensive studies58,1316.
First meridional [CO32–] transect for the LGM Atlantic
We have reconstructed deep-water [CO32–] using benthic B/Ca for
the Holocene (0–5 ka) and LGM samples from 41 cores (Fig. 2 and
Extended Data Figs. 1–3). Five cores at 3.0–4.2 km and an abyssal
core at ~5 km from the South Atlantic were chosen to investigate the
reasons for the 14C and εNd anomalies at 3.8 km water depth (Figs. 1
and 2a). Thirty additional cores from widely spread locations (1.1–
4.7 km, 36° S to 62° N) in the Atlantic and five cores at 3–4 km from
the equatorial Pacific provide a broader context of water-mass sig-
natures. Benthic B/Ca is converted into deep-water [CO32–] using
species-specific global core-top calibrations17. The uncertainty asso-
ciated with [CO32–] reconstructions is ~5 μmol kg–1 (ref. 17). Detailed
information about the samples and analytical methods along with
new (n = 173 samples) and compiled (n = 260 samples) data is given
in Methods and Supplementary Tables 1–7.
Figure 2c shows the first meridional [CO32–] transect for the
deep Atlantic during the LGM (Methods). Given the locations of
the studied cores, this transect mainly reflects [CO32–] distributions
for eastern Atlantic basins. Future work is needed to investigate the
extent of zonal homogeneity in the LGM Atlantic. Above ~2.5 km,
the [CO32–] of glacial North Atlantic waters reached up to ~140 μmol
kg–1, which is ~20 μmol kg–1 higher than in modern North Atlantic
Deep Water (NADW)11. These waters likely represent the previously
Last glacial atmospheric CO2 decline due to
widespread Pacific deep-water expansion
J. Yu 1,2 ✉ , L. Menviel 3, Z. D. Jin 2,4,5, R. F. Anderson 6, Z. Jian7, A. M. Piotrowski8, X. Ma2,
E. J. Rohling 1,9, F. Zhang 2,4, G. Marino1,10 and J. F. McManus6
Ocean circulation critically affects the global climate and atmospheric carbon dioxide through redistribution of heat and carbon
in the Earth system. Despite intensive research, the nature of past ocean circulation changes remains elusive. Here we pres-
ent deep-water carbonate ion concentration reconstructions for widely distributed locations in the Atlantic Ocean, where low
carbonate ion concentrations indicate carbon-rich waters. These data show a low-carbonate-ion water mass that extended
northward up to about 20° S in the South Atlantic at 3–4 km depth during the Last Glacial Maximum. In combination with radio-
carbon ages, neodymium isotopes and carbon isotopes, we conclude that this low-carbonate-ion signal reflects a widespread
expansion of carbon-rich Pacific deep waters into the South Atlantic, revealing a glacial deep Atlantic circulation scheme differ-
ent than commonly considered. Comparison of high-resolution carbonate ion records from different water depths in the South
Atlantic indicates that this Pacific deep-water expansion developed from approximately 38,000 to 28,000 years ago. We infer
that its associated carbon sequestration may have contributed critically to the contemporaneous decline in atmospheric carbon
dioxide, thereby helping to initiate the glacial maximum.
NATURE GEOSCIENCE | VOL 13 | SEPTEMBER 2020 | 628–633 | www.nature.com/naturegeoscience
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... Unlike AA and EB, the large area covered by DAF is somewhat unexpected, as it has often been assumed that cold and dry conditions, which are characteristic of the LGM, led to the spread of open savannas, grasslands and semi-desert landscapes in the Horn of Africa, including the Ethiopian highlands [33][34][35][36] . The simulated extent of DAF attained its maximum at 17-16 ka boosted by low temperatures, and slightly higher precipitations and CO 2 concentrations than during the peak of the LGM 24,37 . DAF extent remained substantial for most of the remaining Late Glacial, only retreating slightly during the interstadial warming (Bølling-Allerød period), notably at 13 ka. ...
... Furthermore, atmospheric CO 2 concentrations must have also played a role in the distribution of habitats. The effect of CO 2 on vegetation must have been significant during the LGM (22-18 ka), when CO 2 levels were below 200 ppm 37 , and gradually became subordinate as CO 2 concentrations approached pre-industrial levels. During the Holocene, CO 2 impact on vegetation distribution is estimated to have been neglectable. ...
... This allows us to calculate the correction factor for each time slice with a given past CO 2 concentration. Past CO 2 concentrations have been taken from the estimates in Yu et al. 37 (Supplementary Table S3). ...
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... Previous studies hypothesized that such old deep water in the Pacific and the Southern Ocean became a source of carbon efflux in the following deglaciation. In fact, it was suggested that glacial Pacific Deep Water (PDW), exported into the Atlantic Ocean via the Drake Passage, played a positive feedback role in increased carbon storage in the South Atlantic during the LGM 25 . However, data directly allowing to quantify deep-water carbon chemistry and distribution are limited to the southwest and equatorial Pacific [26][27][28] , both distal to the Drake Passage and the southernmost South Atlantic. ...
... Because variations in deep-water carbonate ion concentration ([CO 3 2− ]) are primarily governed by DIC and alkalinity, the determination of quantitative [CO 3 2− ] is a means to estimate deep ocean carbon storage. The B/Ca ratio of epifaunal benthic foraminifera, particularly Cibicidoides wuellerstorfi, has so far been the most-often deep-water [CO 3 2− ] proxy, developed on the basis of empirical correlation with the deep-water carbonate saturation state (Δ[CO 3 2− ]) 25,29,30 . For the Pacific sector of the Southern Ocean, B/Ca data from the subpolar Southwest Pacific show a significant decrease of~15 μmol kg -1 in [CO 3 2− ] within the UCDW during the LGM. ...
... A glacial CDW isolated from surrounding water masses was also inferred for the Atlantic Southern Ocean, and explained by a shallower depth and a higher flux of glacial intermediate water 20,51 . Specifically, reconstructions in the subantarctic Southern Atlantic revealed that the Atlantic CDW at the depth of~3800 m showed lower [CO 3 2− ] (~70 μmol kg -1 ) than underlying Atlantic AABW (~90 μmol kg -1 ) at the depth of~5000 m 25 (Fig. 5b), which suggest the isolation of glacial Atlantic CDW from the other water masses. Such Atlantic CDW, which partly originated from glacial NADW, may have been channeled into the South Pacific by the ACC. ...
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... Although details of the mechanisms are still emerging, fluctuations in the atmospheric partial pressure of carbon dioxide (pCO 2-atm ) over the past 800,000 years can be attributed primarily to oceanic processes (Broecker, 1982;Sigman and Boyle, 2000;Lüthi et al., 2008;Sigman et al., 2010;Yu et al., 2020). Various paleoceanographic records from the Western Tropical Pacific (WTP), including productivity (Beaufort et al., 2001;Li et al., 2010;Bolliet et al., 2011;Diester-Haass et al., 2018), deep-water carbonate ion concentrations (Qin et al., 2017(Qin et al., , 2018, redox-sensitive elements (Xiong et al., 2012;Xu et al., 2020), and terrigenous material inputs (Wan et al., 2017;Xu et al., 2020), have been investigated to improve our understanding of the relationships between pCO 2-atm and oceanic conditions, confirming that processes in the WTP play a key role in pCO 2-atm variation. ...
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Surface waters of the modern Western Tropical Pacific (WTP) are in equilibrium with atmospheric CO2. However, air-sea exchange of CO2 in this region may have been modulated in the past by oceanic-atmospheric fluctuations in the tropical Pacific such as the East Asian monsoon and the El Niño-Southern Oscillation (ENSO) and extratropical mode waters such as Antarctic Intermediate Water. Thus, understanding controls on the sea-surface carbonate system in the WTP is important for forecasting future carbon-cycle changes in this region. Here, we reconstruct sea-surface pH and pCO2 since Marine Isotope Stage 6 (MIS 6; 155 ka) based on B/Ca ratios of the planktic foraminifer Globigerinoides ruber (white) in sediment Core MD06–3052 from the western Philippine Sea, and we then calculate the difference between oceanic and atmospheric pCO2 (ΔpCO2(sw-atm)) in order to evaluate the history of air-sea CO2 exchange. ΔpCO2(sw-atm) changes were strongly modulated by the ∼20-kyr precession cycle. The results of cross-spectral analysis demonstrate a close connection between the East Asian summer monsoon (EASM) and air-sea CO2 exchange since MIS 6, demonstrating that precession-driven EASM can affect air-sea CO2 exchange through regulation of surface productivity and thermocline depth. In contrast, the East Asian winter monsoon (EAWM) and ENSO-like conditions are not major influences on air-sea CO2 exchange in the study area at precession-band frequencies. In addition, enhanced upwelling of Southern Ocean-sourced deepwater rich in dissolved inorganic carbon (DIC) affected the upper water column during transitions from cold to warm stages (i.e., deglaciations). In conclusion, these findings suggest that orbital precession influences can affect oceanic conditions not only through climate change and biological processes but also through sea-surface carbonate chemistry.
... In the deep ocean, glacial haline stratification is thought to decrease vertical mixing across water masses as compared to the thermohaline stratification today, leading to more stratification (Adkins, 2013). Aged Glacial Pacific Deep Water can invade the deep South Atlantic through the Drake Passage (DP) (Howe et al., 2016;Williams et al., 2021;Yu et al., 2020). Simultaneously, a reduced Agulhas leakage occurs (Franzese et al., 2006), limiting the influence of the Indian Ocean on the southern Atlantic. ...
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... 62 Indeed, a significant correlation between B/Ca ratio in the shells of Cibicidoides wuellerstorfi 63 and deep seawater Δ[CO 3 2-] was shown by Yu and Elderfield [2007]. The sensitivity of C. 64 wuellerstorfi B/Ca ratio to deep seawater Δ[CO 3 2-] was evaluated based on core-top calibration sufficient amount of benthic foraminifera shells of the target species [e.g., Yu et al., 2016Yu et al., , 2020 Allen et al., 2015,2019]. Next to the most frequently used calibration based on C. wuellerstorfi, 71 there also exist data for another epifaunal species, C. mundulus, confirming a relationship 72 between shell B/Ca and deep seawater Δ[CO 3 2-], but the calibration shows a different slope, 73 indicating that the incorporation of B into the shell calcite is affected by species-specific 74 processes. ...
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The quantitative and objective characterization of dissolution intensity in fossil planktonic foraminiferal shells could be used to reconstruct past changes in bottom water carbonate ion concentration. Among proxies measuring the degree of dissolution of planktonic foraminiferal shells, X-ray micro-Computed Tomography (CT) based characterization of apparent shell density appears to have good potential to facilitate quantitative reconstruction of carbonate chemistry. However, unlike the well-established benthic foraminiferal B/Ca ratio-based proxy, only a regional calibration of the CT-based proxy exists based on a limited number of data points covering mainly low-saturation state waters. Here we determined by CT-based proxy the shell dissolution intensity of planktonic foraminifera Globigerina bulloides, Globorotalia inflata, Globigerinoides ruber, and Trilobatus sacculifer from a collection of core top samples in the Southern Atlantic covering higher saturation states, and assessed the characteristics and reliability of CT-based proxy. We observed that the CT-based proxy is generally controlled by deep-water Δ[CO32–] like the B/Ca proxy, but its effective range of Δ[CO32–] is between –20 to 10 µmolkg–1. In this range, the CT-based proxy appears directly and strongly related to deep-water Δ[CO32–], whereas the B/Ca of benthic foraminifera appears to be affected by porewater saturation in carbonate-rich substrates. On the other hand, the CT-based proxy is affected by supralysoclinal dissolution in areas with high productivity. Like the B/Ca proxy, the CT-based proxy requires species-specific calibration, but the effect of species-specific shell difference in susceptibility to dissolution on the proxy is small.
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The quantitative and objective characterization of dissolution intensity in fossil planktonic foraminiferal shells could be used to reconstruct past changes in bottom water carbonate ion concentration. Among proxies measuring the degree of dissolution of planktonic foraminiferal shells, X‐ray micro‐Computed Tomography (CT) based characterization of apparent shell density appears to have good potential to facilitate quantitative reconstruction of carbonate chemistry. However, unlike the well‐established benthic foraminiferal B/Ca ratio‐based proxy, only a regional calibration of the CT‐based proxy exists based on a limited number of data points covering mainly low‐saturation state waters. Here we determined by CT‐based proxy the shell dissolution intensity of planktonic foraminifera Globigerina bulloides, Globorotalia inflata, Globigerinoides ruber , and Trilobatus sacculifer from a collection of core top samples in the Southern Atlantic covering higher saturation states and assessed the reliability of CT‐based proxy. We observed that the CT‐based proxy is generally controlled by deep‐water Δ[CO 3 2– ] like the B/Ca proxy, but its effective range of Δ[CO 3 2– ] is between –20 to 10 µmolkg –1 . In this range, the CT‐based proxy appears directly and strongly related to deep‐water Δ[CO 3 2– ], whereas we note that in some settings, there appears to be a secondary influence on B/Ca which we suggest may be due to elevated alkalinity from carbonate dissolution in sediments. On the other hand, the CT‐based proxy is affected by supralysoclinal dissolution in areas with high productivity. Like the B/Ca proxy, the CT‐based proxy requires species‐specific calibration, but the effect of species‐specific shell difference in susceptibility to dissolution on the proxy is small. This article is protected by copyright. All rights reserved.
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As the largest reservoir of carbon exchanging with the atmosphere on glacial–interglacial timescales, the deep ocean has been implicated as the likely location of carbon sequestration during Pleistocene glaciations. Despite strong theoretical underpinning for this expectation, radiocarbon data on watermass ventilation ages conflict, and proxy interpretations disagree about the depth, origin and even existence of the respired carbon pool. Because any change in the storage of respiratory carbon is accompanied by corresponding changes in dissolved oxygen concentrations, proxy data reflecting oxygenation are valuable in addressing these apparent inconsistencies. Here, we present a record of redox-sensitive uranium from the central equatorial Pacific Ocean to identify intervals associated with respiratory carbon storage over the past 350 kyr, providing evidence for repeated carbon storage over the last three glacial cycles. We also synthesise our data with previous work and propose an internally consistent picture of glacial carbon storage and equatorial Pacific Ocean watermass structure.
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CO 2 escaped from the deep Why did the concentration of atmospheric carbon dioxide rise so much and so quickly during the last deglaciation? Evidence has begun to accumulate suggesting that old, carbon-rich water accumulated at depth in the Southern Ocean, which then released its charge when Southern Ocean stratification broke down as the climate there warmed. Basak et al. present measurements of neodymium isotopes that clearly show that the deepwater column of the glacial southern South Pacific was stratified, just as would be necessary for the accumulation of old, carbon-rich water. Their data also show that North Atlantic processes were not the dominant control on Southern Ocean water-mass structure during that interval, as has been thought. Science , this issue p. 900