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Over the last decades, sea surface temperature (SST) reconstructions based on the Mg/Ca of foraminiferal calcite have frequently been used in combination with the δ18 O signal from the same material to provide estimates of the δ18 O of water (δ18 O w), a proxy for global ice volume and sea surface salinity (SSS). However, because of error propagation from one step to the next, better calibrations are required to increase the accuracy and robustness of existing isotope and element to temperature proxy relationships. Towards that goal, we determined Mg/Ca , Sr/Ca and the oxygen isotopic composition of Trilobatus sacculifer (previously referenced as Globigerinoides sacculifer) collected from surface waters (0–10 m) along a north–south transect in the eastern basin of the tropical and subtropical Atlantic Ocean. We established a new paleotemperature calibration based on Mg/Ca and on the combination of Mg/Ca and Sr/Ca. Subsequently, a sensitivity analysis was performed in which one, two or three different equations were considered. Results indicate that foraminiferal Mg/Ca allows for an accurate reconstruction of surface water temperature. Combining equations, δ18 O w can be reconstructed with a precision of about ± 0.5 ‰. However, the best possible salinity reconstruction based on locally calibrated equations only allowed for a reconstruction with an uncertainty of ± 2.49. This was confirmed by a Monte Carlo simulation, applied to test successive reconstructions in an "ideal case" in which explanatory variables are known. This simulation shows that from a purely statistical point of view, successive reconstructions involving Mg/Ca and δ18 O c preclude salinity reconstructions with a precision better than ± 1.69 and hardly better than ± 2.65 due to error propagation. Nevertheless, a direct linear fit to reconstruct salinity based on the same measured variables (Mg/Ca and δ18 O c) was established. This direct reconstruction of salinity led to a much better estimation of salinity (± 0.26) than the successive reconstructions. [ABSTRACT FROM AUTHOR]

To date, observations on a single location indicate that cryogenic gypsum (Ca[SO4]⋅2H2O) may constitute an efficient but hitherto overlooked ballasting mineral enhancing the efficiency of the biological carbon pump in the Arctic Ocean. In June–July 2017 we sampled cryogenic gypsum under pack ice in the Nansen Basin north of Svalbard using a plankton net mounted on a remotely operated vehicle (ROVnet). Cryogenic gypsum crystals were present at all sampled stations, which suggested a persisting cryogenic gypsum release from melting sea ice throughout the investigated area. This was supported by a sea ice backtracking model, indicating that gypsum release was not related to a specific region of sea ice formation. The observed cryogenic gypsum crystals exhibited a large variability in morphology and size, with the largest crystals exceeding a length of 1 cm. Preservation, temperature and pressure laboratory studies revealed that gypsum dissolution rates accelerated with increasing temperature and pressure, ranging from 6%d−1 by mass in polar surface water (−0.5°C) to 81 % d−1 by mass in Atlantic Water (2.5°C at 65 bar). When testing the preservation of gypsum in formaldehyde-fixed samples, we observed immediate dissolution. Dissolution at warmer temperatures and through inappropriate preservation media may thus explain why cryogenic gypsum was not observed in scientific samples previously. Direct measurements of gypsum crystal sinking velocities ranged between 200 and 7000 m d−1, suggesting that gypsum-loaded marine aggregates could rapidly sink from the surface to abyssal depths, supporting the hypothesized potential of gypsum as a ballasting mineral in the Arctic Ocean. [ABSTRACT FROM AUTHOR]