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[1] Acidified waters are impacting commercial oyster production in the U.S. Pacific Northwest, and favorable carbonate chemistry conditions are predicted to become less frequent. Within 48 h of fertilization, unshelled Pacific oyster (Crassostrea gigas) larvae precipitate roughly 90% of their body weight as calcium carbonate. We measured stable carbon isotopes in larval shell and tissue and in algal food and seawater dissolved inorganic carbon in a longitudinal study of larval development and growth. Using these data and measured biochemical composition of larvae, we show that sensitivity of initial shell formation to ocean acidification results from diminished ability to isolate calcifying fluid from surrounding seawater, a limited energy budget and a strong kinetic demand for calcium carbonate precipitation. Our results highlight an important link between organism physiology and mineral kinetics in larval bivalves and suggest the consideration of mineral kinetics may improve understanding winners and losers in a high CO 2 world.

shelf-and river-derived elements to the central Arctic Ocean • The TPD is rich in dissolved organic matter (DOM), which facilitates long-range transport of trace metals that form complexes with DOM • Margin trace element fluxes may increase with future Arctic warming due to DOM release from permafrost thaw and increasing river discharge

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[1] The isotopic composition of the dissolved inorganic carbon (DIC) collected at sites of active methane discharge on Hydrate Ridge, Oregon, reveals anaerobic methane oxidation mediated by bacteria, with d 13 C DIC reaching values as low as À48% in the upper 4 cm of the sediment. In spite of the high sulfide levels in the discharging fluids, living specimens of the benthic foraminifera Uvigerina peregrina are abundant in the vents, probably owing to the rich bacterial food source. Although pore water d 13 C DIC is extremely low (À6 to À48%), the d 13 C values of living (Rose Bengal stained) foraminifera shells collected from active methane seeps are not significantly lower than those observed in nonventing pelagic sediments, and are within the range expected from local organic matter decomposition (0 to À4%). The apparent d 13 C disequilibrium between biogenic calcite and DIC suggests that at seep localities, foraminifera calcify mostly during periods when there is little methane discharge or during intermittent episodes of seawater flow into the sediments. The isotopic composition and Mg/ Ca ratios of fossil (unstained) foraminifera recovered at carbonate-rich sites on the northern Hydrate Ridge reveals overprinting of the biogenic record by inorganic calcite with high Mg/Ca and anomalously low d 13 C values. Thus overprinting of the original isotopic composition of foraminifera by overgrowths or recrystallization at or below the sediment surface, rather than primary calcification in contact with 13 C depleted DIC, can explain extreme 13 C depletion observed in fossil foraminifera recovered from sites of active methane discharge.