Calcium carbonate (CaCO ₃ ) biomineralizing organisms have played major roles in the history of life and the global carbon cycle during the past 541 Ma. Both marine diversification and mass extinctions reflect physiological responses to environmental changes through time. An integrated understanding of carbonate biomineralization is necessary to illuminate this evolutionary record and to understand how modern organisms will respond to 21st century global change. Biomineralization evolved independently but convergently across phyla, suggesting a unity of mechanism that transcends biological differences. In this review, we combine CaCO ₃ skeleton formation mechanisms with constraints from evolutionary history, omics, and a meta-analysis of isotopic data to develop a plausible model for CaCO ₃ biomineralization applicable to all phyla. The model provides a framework for understanding the environmental sensitivity of marine calcifiers, past mass extinctions, and resilience in 21st century acidifying oceans. Thus, it frames questions about the past, present, and future of CaCO ₃ biomineralizing organisms.

Quantifying variability in the ocean carbon sink remains problematic due to sparse observations and spatiotemporal variability in surface ocean pCO₂. To address this challenge, we have updated and improved ECCO‐Darwin, a global ocean biogeochemistry model that assimilates both physical and biogeochemical observations. The model consists of an adjoint‐based ocean circulation estimate from the Estimating the Circulation and Climate of the Ocean (ECCO) consortium and an ecosystem model developed by the Massachusetts Institute of Technology Darwin Project. In addition to the data‐constrained ECCO physics, a Green's function approach is used to optimize the biogeochemistry by adjusting initial conditions and six biogeochemical parameters. Over seasonal to multidecadal timescales (1995–2017), ECCO‐Darwin exhibits broad‐scale consistency with observed surface ocean pCO₂ and air‐sea CO₂ flux reconstructions in most biomes, particularly in the subtropical and equatorial regions. The largest differences between CO₂ uptake occur in subpolar seasonally stratified biomes, where ECCO‐Darwin results in stronger winter uptake. Compared to the Global Carbon Project OBMs, ECCO‐Darwin has a time‐mean global ocean CO₂ sink (2.47 ± 0.50 Pg C year⁻¹) and interannual variability that are more consistent with interpolation‐based products. Compared to interpolation‐based methods, ECCO‐Darwin is less sensitive to sparse and irregularly sampled observations. Thus, ECCO‐Darwin provides a basis for identifying and predicting the consequences of natural and anthropogenic perturbations to the ocean carbon cycle, as well as the climate‐related sensitivity of marine ecosystems. Our study further highlights the importance of physically consistent, property‐conserving reconstructions, as are provided by ECCO, for ocean biogeochemistry studies.

Using new and published marine fossil radiocarbon ( ¹⁴ C/C) measurements, a tracer uniquely sensitive to circulation and air-sea gas exchange, we establish several benchmarks for Atlantic, Southern, and Pacific deep-sea circulation and ventilation since the last ice age. We find the most ¹⁴ C-depleted water in glacial Pacific bottom depths, rather than the mid-depths as they are today, which is best explained by a slowdown in glacial deep-sea overturning in addition to a “flipped” glacial Pacific overturning configuration. These observations cannot be produced by changes in air-sea gas exchange alone, and they underscore the major role for changes in the overturning circulation for glacial deep-sea carbon storage in the vast Pacific abyss and the concomitant drawdown of atmospheric CO ₂ .

The inventory and variability of oceanic dissolved inorganic carbon (DIC) is driven by the interplay of physical, chemical, and biological processes. Quantifying the spatiotemporal variability of these drivers is crucial for a mechanistic understanding of the ocean carbon sink and its future trajectory. Here, we use the Estimating the Circulation and Climate of the Ocean‐Darwin ocean biogeochemistry state estimate to generate a global‐ocean, data‐constrained DIC budget and investigate how spatial and seasonal‐to‐interannual variability in three‐dimensional circulation, air‐sea CO ₂ flux, and biological processes have modulated the ocean sink for 1995–2018. Our results demonstrate substantial compensation between budget terms, resulting in distinct upper‐ocean carbon regimes. For example, boundary current regions have strong contributions from vertical diffusion while equatorial regions exhibit compensation between upwelling and biological processes. When integrated across the full ocean depth, the 24‐year DIC mass increase of 64 Pg C (2.7 Pg C year ⁻¹ ) primarily tracks the anthropogenic CO ₂ growth rate, with biological processes providing a small contribution of 2% (1.4 Pg C). In the upper 100 m, which stores roughly 13% (8.1 Pg C) of the global increase, we find that circulation provides the largest DIC gain (6.3 Pg C year ⁻¹ ) and biological processes are the largest loss (8.6 Pg C year ⁻¹ ). Interannual variability is dominated by vertical advection in equatorial regions, with the 1997–1998 El Niño‐Southern Oscillation causing the largest year‐to‐year change in upper‐ocean DIC (2.1 Pg C). Our results provide a novel, data‐constrained framework for an improved mechanistic understanding of natural and anthropogenic perturbations to the ocean sink.

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.

The δ³⁴S of seawater sulfate reflects processes operating at the nexus of sulfur, carbon, and oxygen cycles. However, knowledge of past seawater sulfate δ³⁴S values must be derived from proxy materials that are impacted differently by depositional and postdepositional processes. We produced new time series estimates for the δ³⁴S value of seawater sulfate by combining 6,710 published data from three sedimentary archives—marine barite, evaporites, and carbonate‐associated sulfate—with updated age constraints on the deposits. Robust features in multiple records capture temporal trends in the δ³⁴S value of seawater and its interplay with other Phanerozoic geochemical and stratigraphic trends. However, high‐frequency discordances indicate that each record is differentially prone to depositional biases and diagenetic overprints. The amount of noise, quantified from the variograms of each record, increases with age for all δ³⁴S proxies, indicating that postdepositional processes obscure detailed knowledge of seawater sulfate's δ³⁴S value deeper in time.