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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.
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Pedogenic carbonate as a transient soil component in a humid, temperate forest (Michigan, USA)
In humid, continental Michigan, we identified pedogenic carbonate in a soil profile developed on glacial drift sediments, as rinds, rhizoliths, and filaments (at depths >50 cm). Given that the climate setting is unusual for pedogenic carbonate, we investigated its formation with environmental monitoring and isotope analyses of carbonate (δ13C, δ18O, Δ47, and 14C) and waters (δ18O and δ2H). We found covariation in δ13C and Δ47 amongst the carbonate types (rhizoliths, rinds, filaments, bulk soil, and detrital clasts), and 14C ages of rinds that predate plausible formation ages. The δ13C and Δ47 values of the bulk carbonate and some of the pedogenic morphologies are not fully compatible with pedogenic formation in the modern environment. The δ18O data from precipitation and river waters and from carbonates are not uniquely identifying; they are compatible with the soil carbonate being pedogenic, detrital, or a mix. We conclude that the soil carbonate is likely a physical mix of pedogenic and detrital carbonate. Pedogenic carbonate is forming in this humid setting, likely because seasonal cycles in soil respiration and temperature cause cycles of dissolution and re-precipitation of detrital and pedogenic carbonate. The pedogenic carbonate may be a transient feature as carbonate-rich till undergoes post-glacial chemical weathering.
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- Award ID(s):
- 2122023
- PAR ID:
- 10562829
- Publisher / Repository:
- Cambridge University Press
- Date Published:
- Journal Name:
- Quaternary research
- ISSN:
- 1096-0287
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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