Description: The Arctic Ocean is an exceptional environment where hydrosphere, cryosphere, and atmosphere are closely interconnected. Changes in sea-ice extent and thickness affect ocean currents, as well as moisture and heat exchange with the atmosphere. Energy and water fluxes impact the formation and melting of sea ice and snow cover. Here, we present a comprehensive statistical analysis of the stable water isotopes of various hydrological components in the central Arctic obtained during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition in 2019–2020, including the understudied Arctic winter. Our dataset comprises >2200 water, snow, and ice samples. Snow had the most depleted and variable isotopic composition, with δ18O (–16.3‰) increasing consistently from surface (–22.5‰) to bottom (–9.7‰) of the snowpack, suggesting that snow metamorphism and wind-induced transport may overprint the original precipitation isotope values. In the Arctic Ocean, isotopes also help to distinguish between different sea-ice types, and whether there is a meteoric contribution. The isotopic composition and salinity of surface seawater indicated relative contributions from different freshwater sources: lower δ18O (approximately –3.0‰) and salinities were observed near the eastern Siberian shelves and towards the center of the Transpolar Drift due to river discharge. Higher δ18O (approximately –1.5‰) and salinities were associated with an Atlantic source when the RV Polarstern crossed the Gakkel Ridge into the Nansen Basin. These changes were driven mainly by the shifts within the Transpolar Drift that carried the Polarstern across the Arctic Ocean. Our isotopic analysis highlights the importance of investigating isotope fractionation effects, for example, during sea-ice formation and melting. A systematic full-year sampling for water isotopes from different components strengthens our understanding of the Arctic water cycle and provides crucial insights into the interaction between atmosphere, sea ice, and ocean and their spatio-temporal variations during MOSAiC.

Description: Surface processes alter the water stable isotope signal of the surface snow after deposition. However, it remains an open question to which extent surface post-depositional processes should be considered when inferring past climate information from ice core records. Here, we present simulations for the Greenland Ice Sheet, combining outputs from two climate models with an isotope-enabled snowpack model. We show that surface vapor exchange and associated fractionation imprint a climate signal into the firn, resulting in an increase in the annual mean value of δ18O by +2.3‰ and a reduction in d-excess by −6.3‰. Further, implementing isotopic fractionation during surface vapor exchange improves the representation of the observed seasonal amplitude in δ18O from 65.0% to 100.2%. Our results stress that surface vapor exchange is important in the climate proxy signal formation and needs consideration when interpreting ice core climate records.

Description: Mineral dust accumulated on the ocean floor is an important archive for reconstructing past atmospheric circulation changes and climatological conditions in the source areas. Dust emitted from Southern Hemisphere dust sources is widely deposited over the oceans. However, there are few records of dust deposition over the open ocean, and a large need for extended geographical coverage exists. We present a large data set (134 surface sediment samples) of Late Holocene dust deposition from seafloor surface sediments covering the entire South Atlantic Ocean. Polymodal grain-size distributions of the lithogenic fraction indicate that the sediments are composed of multiple sediment components. By using end-member modeling, we attempt to disentangle the dust signal from non-aeolian sediments. Combined with 230Th-normalized lithogenic fluxes, we quantified the specific deposition fluxes for mineral dust, crrent-sorted sediments and ice-rafted debris (IRD). Although the method could not completely separate the different components in every region, it shows that dust deposition off the most prominent dust source for the South Atlantic Ocean—southern South America—amounts up to approximately 0.7 g cm−2 Kyr−1 and decreases downwind. Bottom-current-sorted sediments and IRD are mostly concentrated around the continental margins. The ratio of the coarse to fine dust end members reveals input from north African dust sources to the South Atlantic. The majority of the observations are in good agreement with new model simulations. This extensive and relevant data set of dust grain size and deposition fluxes to the South Atlantic could be used to calibrate and validate further model simulations.

Description: The Arctic Ocean is an exceptional environment where hydrosphere, cryosphere, and atmosphere are closely interconnected. Changes in sea-ice extent and thickness affect ocean currents, as well as moisture and heat exchange with the atmosphere. Energy and water fluxes impact the formation and melting of sea ice and snow cover. Here, we present a comprehensive statistical analysis of the stable water isotopes of various hydrological components in the central Arctic obtained during the Multidisciplinary drifting Observatory for the Study of Arctic Climate (MOSAiC) expedition in 2019–2020, including the understudied Arctic winter. Our dataset comprises 〉2200 water, snow, and ice samples. Snow had the most depleted and variable isotopic composition, with d18O (–16.3%) increasing consistently from surface (–22.5%) to bottom (–9.7%) of the snowpack, suggesting that snow metamorphism and wind-induced transport may overprint the original precipitation isotope values. In the Arctic Ocean, isotopes also help to distinguish between different sea-ice types, and whether there is a meteoric contribution. The isotopic composition and salinity of surface seawater indicated relative contributions from different freshwater sources: lower d18O (approximately –3.0%) and salinities were observed near the eastern Siberian shelves and towards the center of the Transpolar Drift due to river discharge. Higher d18O (approximately –1.5%) and salinities were associated with an Atlantic source when the RV Polarstern crossed the Gakkel Ridge into the Nansen Basin. These changes were driven mainly by the shifts within the Transpolar Drift that carried the Polarstern across the Arctic Ocean. Our isotopic analysis highlights the importance of investigating isotope fractionation effects, for example, during sea-ice formation and melting. A systematic full-year sampling for water isotopes from different components strengthens our understanding of the Arctic water cycle and provides crucial insights into the interaction between atmosphere, sea ice, and ocean and their spatio-temporal variations during MOSAiC.

Description: The products from the Stable Water Isotope Intercomparison Group, Phase 2, are currently used for numerous studies, allowing water isotope model-data comparisons with various isotope-enabled atmospheric general circulation model (AGCMs) outputs. However, the simulations under this framework were performed using different parameterizations and forcings. Therefore, a uniform experimental design with state-of-the-art AGCMs is required to interpret isotope observations rigorously. Here, we evaluate the outputs from three isotope-enabled numerical models nudged by three different reanalysis products and investigate the ability of the isotope-enabled AGCMs to reproduce the spatial and temporal patterns of water isotopic composition observed at the surface and in the atmospheric airborne water. Through correlation analyses at various spatial and temporal scales, we found that the model's performance depends on the model or reanalysis we use, the observations we compare, and the vertical levels we select. Moreover, we employed the stable isotope mass balance method to conduct decomposition analyses on the ratio of isotopic changes in the atmosphere. Our goal was to elucidate the spread in simulated atmospheric column δ18O, which is influenced by factors such as evaporation, precipitation, and horizontal moisture flux. Satisfying the law of conservation of water isotopes, this budget method is expected to explain various fractionation phenomena in atmospheric meteorological and climatic events. It also aims to highlight the spreads in modeled isotope results among different experiments using multiple models and reanalyses, which are primarily dominated by uncertainties in moisture flux and precipitation, respectively.

Description: Based on a 6-year long record (2014–2020) of the isotopic composition of rain (δ18Op) at Réunion Island (55°E, 22°S), in the South-West Indian Ocean, this study shows that the annual isotopic composition of precipitation in this region is strongly controlled by the number of cyclones, the number of best-track days, and the proportion of cyclonic rain during the year. Our results support the use of δ18Op in annual-resolved tropical climate archives as a reliable proxy of past cyclone frequency. The influence of the proportion of cyclonic rain on the annual isotopic composition arises from the systematically more depleted precipitation and water vapor during cyclonic events than during less organized convective systems. The analysis of the daily to hourly isotopic composition of water vapor (δ18Ov) during low-pressure systems and the reproduction of daily δ18Ov observations by AGCMs with a global medium to coarse resolution (LMDZ-iso and ECHAM6-wiso) suggest that during cyclonic periods the stronger depletion mainly arises from both enhanced large-scale precipitation and water vapor-rain interactions under humid conditions.