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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. 

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

Abstract Planktonic calcifying organisms play a key role in regulating ocean carbonate chemistry and atmospheric CO₂. 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 (CaCO₃) standing stock, with coccolithophore calcite comprising ~90% of total CaCO₃production, and pteropods and foraminifera playing a secondary role. We show that pelagic CaCO₃production is higher than the sinking flux of CaCO₃at 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 CaCO₃production derived from satellite observations/biogeochemical modeling versus estimates from shallow sediment traps. We suggest future changes in the CaCO₃cycle and its impact on atmospheric CO₂will largely depend on how the poorly-understood processes that determine whether CaCO₃is remineralised in the photic zone or exported to depth respond to anthropogenic warming and acidification. 

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. 

Increasing numbers of gender-nonconforming children are socially transitioning—changing pronouns to live as their identified genders. We studied a cohort of gender-nonconforming children ( n = 85) and contacted them again approximately 2 years later. When recontacted, 36 of the children had socially transitioned. We found that stronger cross-sex identification and preferences expressed by gender-nonconforming children at initial testing predicted whether they later socially transitioned. We then compared the gender-nonconforming children with groups of transitioned transgender children ( n = 84) and gender-conforming controls ( n = 85). Children from our longitudinal cohort who would later transition were highly similar to transgender children (children who had already socially transitioned) and to control children of the gender to which they would eventually transition. Gender-nonconforming children who would not go on to transition were different from these groups. These results suggest that (a) social transitions may be predictable from gender identification and preferences and (b) gender identification and preferences may not meaningfully differ before and after social transitions. 

Abstract North Pacific atmospheric and oceanic circulations are key missing pieces in our understanding of the reorganization of the global climate system since the Last Glacial Maximum. Here, using a basin‐wide compilation of planktic foraminiferal δ¹⁸O, we show that the North Pacific subpolar gyre extended ~3° further south during the Last Glacial Maximum, consistent with sea surface temperature and productivity proxy data. Climate models indicate that the expansion of the subpolar gyre was associated with a substantial gyre strengthening, and that these gyre circulation changes were driven by a southward shift of the midlatitude westerlies and increased wind stress from the polar easterlies. Using single‐forcing model runs, we show that these atmospheric circulation changes are a nonlinear response to ice sheet topography/albedo and CO₂. Our reconstruction indicates that the gyre boundary (and thus westerly winds) began to migrate northward at ~16.5 ka, driving changes in ocean heat transport, biogeochemistry, and North American hydroclimate. 

Abstract The cycling of biologically produced calcium carbonate (CaCO₃) in the ocean is a fundamental component of the global carbon cycle. Here, we present experimental determinations of in situ coccolith and foraminiferal calcite dissolution rates. We combine these rates with solid phase fluxes, dissolved tracers, and historical data to constrain the alkalinity cycle in the shallow North Pacific Ocean. The in situ dissolution rates of coccolithophores demonstrate a nonlinear dependence on saturation state. Dissolution rates of all three major calcifying groups (coccoliths, foraminifera, and aragonitic pteropods) are too slow to explain the patterns of both CaCO₃sinking flux and alkalinity regeneration in the North Pacific. Using a combination of dissolved and solid‐phase tracers, we document a significant dissolution signal in seawater supersaturated for calcite. Driving CaCO₃dissolution with a combination of ambient saturation state and oxygen consumption simultaneously explains solid‐phase CaCO₃flux profiles and patterns of alkalinity regeneration across the entire N. Pacific basin. We do not need to invoke the presence of carbonate phases with higher solubilities. Instead, biomineralization and metabolic processes intimately associate the acid (CO₂) and the base (CaCO₃) in the same particles, driving the coupled shallow remineralization of organic carbon and CaCO₃. The linkage of these processes likely occurs through a combination of dissolution due to zooplankton grazing and microbial aerobic respiration within degrading particle aggregates. The coupling of these cycles acts as a major filter on the export of both organic and inorganic carbon to the deep ocean.