Systematic changes in the chemistry of evaporated seawater contained in primary fluid inclusions in marine halites indicate that seawater chemistry has fluctuated during the Phanerozoic. The fluctuations are in phase with oscillations in seafloor spreading rates, volcanism, global sea level, and the primary mineralogies of marine limestones and evaporites. The data suggest that seawater had high Mg ²⁺ /Ca ²⁺ ratios (>2.5) and relatively high Na ⁺ concentrations during the Late Precambrian [544 to 543 million years ago (Ma)], Permian (258 to 251 Ma), and Tertiary through the present (40 to 0 Ma), when aragonite and MgSO ₄ salts were the dominant marine precipitates. Conversely, seawater had low Mg ²⁺ /Ca ²⁺ ratios (<2.3) and relatively low Na ⁺ concentrations during the Cambrian (540 to 520 Ma), Silurian (440 to 418 Ma), and Cretaceous (124 to 94 Ma), when calcite was the dominant nonskeletal carbonate and K-, Mg-, and Ca-bearing chloride salts, were the only potash evaporites.

The geological record encodes the relationship between climate and atmospheric carbon dioxide (CO ₂ ) over long and short timescales, as well as potential drivers of evolutionary transitions. However, reconstructing CO ₂ beyond 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 CO ₂ record 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 CO ₂ thresholds in biological and cryosphere evolution.

Quantification of the atmospheric concentration of CO2 ([CO2]atm) during warm periods of Earth's history is important because burning of fossil fuels may produce future [CO2]atm approaching 1000 parts per million by volume (ppm). The early Eocene (~56 to 49 million years ago) had the highest prolonged global temperatures of the past 65 million years. High Eocene [CO2]atm is established from sodium carbonate minerals formed in saline lakes and preserved in the Green River Formation, western United States. Coprecipitation of nahcolite (NaHCO3) and halite (NaCl) from surface waters in contact with the atmosphere indicates [CO2]atm > 1125 ppm (four times preindustrial concentrations), which confirms that high [CO2]atm coincided with Eocene warmth.