Lower atmospheric CO2concentrations during the Last Glacial Maximum (LGM; 23.0–18.0 ka) have been attributed to the sequestration of respired carbon in the ocean interior, yet the mechanism responsible for the release of this CO2during the deglaciation remains uncertain. Here we present calculations of vertical differences in oxygen and carbon isotopes (∆δ18O and ∆δ13C, respectively) from a depth transect of southwest Pacific Ocean sediment cores to reconstruct changes in water mass structure and CO2storage. During the Last Glacial Maximum, ∆δ18O indicates a more homogenous deep Pacific below 1,100 m, whereas regional ∆δ13C elucidates greater sequestration of CO2in two distinct layers: enhanced CO2storage at intermediate depths between ~940 and 1,400 m, and significantly more CO2at 1,600 m and below. This highlights an isolated glacial intermediate water mass and places the main geochemical divide at least 500 m shallower than the Holocene. During the initial stages of the deglaciation in Heinrich Stadial 1 (17.5–14.5 ka), restructuring of the upper ~2,000 m of the southwest Pacific water column coincided with sea‐ice retreat and rapid CO2release from intermediate depths, while CO2release from the deep ocean was earlier and more gradual than waters above it. These changes suggest that sea‐ice retreat and shifts in Southern Ocean frontal locations contributed to rapid CO2ventilation from the Southern Ocean's intermediate depths and gradual ventilation from the deep ocean during the early deglaciation.
The deep ocean releases large amounts of old, pre‐industrial carbon dioxide (CO2) to the atmosphere through upwelling in the Southern Ocean, which counters the marine carbon uptake occurring elsewhere. This Southern Ocean CO2release is relevant to the global climate because its changes could alter atmospheric CO2levels on long time scales, and also affects the present‐day potential of the Southern Ocean to take up anthropogenic CO2. Here, year‐round profiling float measurements show that this CO2release arises from a zonal band of upwelling waters between the Subantarctic Front and wintertime sea‐ice edge. This band of high CO2subsurface water coincides with the outcropping of the 27.8 kg m−3isoneutral density surface that characterizes Indo‐Pacific Deep Water (IPDW). It has a potential partial pressure of CO2exceeding current atmospheric CO2levels (∆PCO2) by 175 ± 32 μatm. Ship‐based measurements reveal that IPDW exhibits a distinct ∆PCO2maximum in the ocean, which is set by remineralization of organic carbon and originates from the northern Pacific and Indian Ocean basins. Below this IPDW layer, the carbon content increases downwards, whereas ∆PCO2decreases. Most of this vertical ∆PCO2decline results from decreasing temperatures and increasing alkalinity due to an increased fraction of calcium carbonate dissolution. These two factors limit the CO2outgassing from the high‐carbon content deep waters on more southerly surface outcrops. Our results imply that the response of Southern Ocean CO2fluxes to possible future changes in upwelling are sensitive to the subsurface carbon chemistry set by the vertical remineralization and dissolution profiles.
more » « less- Award ID(s):
- 1936222
- NSF-PAR ID:
- 10445942
- Publisher / Repository:
- DOI PREFIX: 10.1029
- Date Published:
- Journal Name:
- Global Biogeochemical Cycles
- Volume:
- 36
- Issue:
- 7
- ISSN:
- 0886-6236
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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