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Abstract Planktonic foraminifera are key contributors to the oceanic carbon cycle. In pelagic environments, carbonate production by planktonic biomineralizers regulates ocean-atmosphere carbon dioxide exchange and exports surface carbon to the deep ocean. Here we compare shell traits of three planktonic foraminifera species from the central Atlantic with a suite of environmental parameters to discern the factors underlying their variations. Our analysis revealed that calcification in foraminifera is associated with seawater density and depends on species habitat depth, whereas foraminifera bulk shell densities may serve as a seawater density proxy, regardless of species. We observe that their shell weights increased with habitat depth, enabling the living cells to adjust their overall density to match that of the surrounding liquid. This suggests that calcification in nonmotile organisms has a buoyancy regulatory function and will respond to the anthropogenically driven reductions in ocean density (oceanic rarefication), with potential consequences for the carbon cycle. 

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. 

Abstract Planktonic calcifying organisms play a key role in regulating ocean carbonate chemistry and atmospheric CO 2 . Surprisingly, references to the absolute and relative contribution of these organisms to calcium carbonate production are lacking. Here we report quantification of pelagic calcium carbonate production in the North Pacific, providing new insights on the contribution of the three main planktonic calcifying groups. Our results show that coccolithophores dominate the living calcium carbonate (CaCO 3 ) standing stock, with coccolithophore calcite comprising ~90% of total CaCO 3 production, and pteropods and foraminifera playing a secondary role. We show that pelagic CaCO 3 production is higher than the sinking flux of CaCO 3 at 150 and 200 m at ocean stations ALOHA and PAPA, implying that a large portion of pelagic calcium carbonate is remineralised within the photic zone; this extensive shallow dissolution explains the apparent discrepancy between previous estimates of CaCO 3 production derived from satellite observations/biogeochemical modeling versus estimates from shallow sediment traps. We suggest future changes in the CaCO 3 cycle and its impact on atmospheric CO 2 will largely depend on how the poorly-understood processes that determine whether CaCO 3 is remineralised in the photic zone or exported to depth respond to anthropogenic warming and acidification. 

A compilation of radiocarbon measurements is used to characterize deep-sea overturning since the last ice age. 

Throughout Earth's history, CO 2 is thought to have exerted a fundamental control on environmental change. Here we review and revise CO 2 reconstructions from boron isotopes in carbonates and carbon isotopes in organic matter over the Cenozoic—the past 66 million years. We find close coupling between CO 2 and climate throughout the Cenozoic, with peak CO 2 levels of ∼1,500 ppm in the Eocene greenhouse, decreasing to ∼500 ppm in the Miocene, and falling further into the ice age world of the Plio–Pleistocene. Around two-thirds of Cenozoic CO 2 drawdown is explained by an increase in the ratio of ocean alkalinity to dissolved inorganic carbon, likely linked to a change in the balance of weathering to outgassing, with the remaining one-third due to changing ocean temperature and major ion composition. Earth system climate sensitivity is explored and may vary between different time intervals. The Cenozoic CO 2 record highlights the truly geological scale of anthropogenic CO 2 change: Current CO 2 levels were last seen around 3 million years ago, and major cuts in emissions are required to prevent a return to the CO 2 levels of the Miocene or Eocene in the coming century. ▪  CO 2 reconstructions over the past 66 Myr from boron isotopes and alkenones are reviewed and re-evaluated. ▪  CO 2 estimates from the different proxies show close agreement, yielding a consistent picture of the evolution of the ocean-atmosphere CO 2 system over the Cenozoic. ▪  CO 2 and climate are coupled throughout the past 66 Myr, providing broad constraints on Earth system climate sensitivity. ▪  Twenty-first-century carbon emissions have the potential to return CO 2 to levels not seen since the much warmer climates of Earth's distant past. 

The geological record encodes the relationship between climate and atmospheric carbon dioxide (CO₂) over long and short timescales, as well as potential drivers of evolutionary transitions. However, reconstructing CO₂beyond direct measurements requires the use of paleoproxies and herein lies the challenge, as proxies differ in their assumptions, degree of understanding, and even reconstructed values. In this study, we critically evaluated, categorized, and integrated available proxies to create a high-fidelity and transparently constructed atmospheric CO₂record spanning the past 66 million years. This newly constructed record provides clearer evidence for higher Earth system sensitivity in the past and for the role of CO₂thresholds in biological and cryosphere evolution.