77 research outputs found

    Seasonality in Saharan Dust Across the Atlantic Ocean: From Atmospheric Transport to Seafloor Deposition

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    Saharan dust is transported in great quantities from the North African continent every year, most of which is deposited across the North Atlantic Ocean. This dust impacts regional and global climate by affecting the atmospheric radiation balance and altering ocean carbon budgets. However, little research has been carried out on time series of Saharan dust collected in situ across the open Atlantic. Here, we present a unique three-year time series of Saharan dust along a trans-Atlantic transect, sampled by moored surface buoys and subsurface sediment traps. Results show a good correlation between the particle-size distributions of atmospheric dust and the lithogenic particles settling to the deep ocean floor, confirming the aeolian origin of the lithogenic particles intercepted by the subsurface sediment traps, even in the distal western part of the Atlantic Ocean. Dust from both dry and wet deposition as collected by the sediment traps, shows increased deposition fluxes and coarser grain size in summer and/or autumn that coincides with increased precipitation at the sampling sites as derived from satellite data. In contrast, both buoys that sampled dust during transport at sea level show little seasonal variation in both concentration and particle size, as the large amounts of dust transported in summer and early autumn at high altitudes are far above their sampling range. This implies that wet deposition in summer and autumn defines the typical seasonal trends of both the dust deposition flux and its particle-size distribution observed in the sediment traps

    Environmental factors controlling the seasonal variability in particle size distribution of modern Saharan dust deposited off Cape Blanc

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    The particle sizes of Saharan dust in marine sediment core records have been used frequently as a proxy for trade-wind speed. However, there are still large uncertainties with respect to the seasonality of the particle sizes of deposited Saharan dust off northwestern Africa and the factors influencing this seasonality. We investigated a three-year time-series of grain-size data from two sediment-trap moorings off Cape Blanc, Mauritania and compared them to observed wind-speed and precipitation as well as satellite images. Our results indicate a clear seasonality in the grain-size distributions: during summer the modal grain sizes were generally larger and the sorting was generally less pronounced compared to the winter season. Gravitational settling was the major deposition process during winter. We conclude that the following two mechanisms control the modal grain size of the collected dust during summer: (1) wet deposition causes increased deposition fluxes resulting in coarser modal grain sizes and (2) the development of cold fronts favors the emission and transport of coarse particles off Cape Blanc. Individual dust-storm events throughout the year could be recognized in the traps as anomalously coarse-grained samples. During winter and spring, intense cyclonic dust-storm events in the dust-source region explained the enhanced emission and transport of a larger component of coarse particles off Cape Blanc. The outcome of our study provides important implications for climate modellers and paleo-climatologists

    Sample intervals, positions of sampling, and modal particle size of sediment-trap samples, shipboard-collected aerosol samples and Mauritanian soil samples

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    Large amounts of mineral dust are exported from North Africa across the Atlantic Ocean, impacting the atmosphere and ocean during transport and after deposition through biogeochemical processes. In order to characterize the isotopic signature of dust from different seasons and years, in relation to their bulk particle size, and to obtain a general idea of its provenance, Saharan dust was collected using subsurface sediment traps moored in the tropical North Atlantic Ocean in 2012–2013, and by shipboard aerosol collection during three trans-Atlantic research cruises in 2005, 2012 and 2015. The samples were analysed for radiogenic Strontium (Sr), Neodymium (Nd), and Hafnium (Hf) isotopes, rare earth element (REE; La-Lu) abundances and particle size. In addition, soil sediments from Mauritania, a potential source area, were analysed and compared to the Atlantic dust samples. The results indicate no relation between Sr and Nd isotopic compositions and dust particle size. In contrast, Hf isotopic compositions show a strong relation with particle size, associated to the so-called zircon effect. We explored alternative sources of lithogenic particles to the sediment traps such as Amazon River sediments. Our results reveal that the sediment-trap samples bear distinctly different geochemical signatures from sediments from the Amazon Basin and Amazon River tributaries, and confirm that the primary source of lithogenic particles is northern Africa. The collected dust samples show close relations to African dust aerosols collected at Barbados and samples from the Bodélé Depression, although differences between seasons are observed, which we relate to differences in source areas

    Sr-Nd-Hf isotopes, REEs and particle size of dust collected across the Atlantic Ocean

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    Saharan dust was collected using subsurface sediment traps mooried in the tropical North Atlantic Ocean in 2012-2013, and by shipboard aerosol collection during three trans-Atlantic research cruises in 2005, 2012 and 2015. The samples were analysed for radiogenic Strontium (Sr), Neodymium (Nd), and Hafnium (Hf) isotopes, rare earth element (REE; La-Lu) abundances and particle size. In addition, soil sediments from Mauritania, a potential source area, were analysed

    Simulating glacial dust changes in the Southern Hemisphere using ECHAM6.3-HAM2.3

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    Mineral dust aerosol constitutes an important component of the Earth’s climate system, not only on short timescales due to direct and indirect influences on the radiation budget but also on long timescales by acting as a fertilizer for the biosphere and thus affecting the global carbon cy- cle. For a quantitative assessment of its impact on the global climate, state-of-the-art atmospheric and aerosol models can be utilized. In this study, we use the ECHAM6.3-HAM2.3 model to perform global simulations of the mineral dust cy- cle for present-day (PD), pre-industrial (PI), and last glacial maximum (LGM) climate conditions. The intercomparison with marine sediment and ice core data, as well as other mod- eling studies, shows that the obtained annual dust emissions of 1221, 923, and 5159 Tg for PD, PI, and LGM, respectively, generally agree well with previous findings. Our analyses fo- cusing on the Southern Hemisphere suggest that over 90 % of the mineral dust deposited over Antarctica are of Australian or South American origin during both PI and LGM. How- ever, contrary to previous studies, we find that Australia con- tributes a higher proportion during the LGM, which is mainly caused by changes in the precipitation patterns. Obtained in- creased particle radii during the LGM can be traced back to increased sulfate condensation on the particle surfaces as a consequence of longer particle lifetimes. The meridional transport of mineral dust from its source regions to the South Pole takes place at different altitudes depending on the grain size of the dust particles. We find a trend of generally lower transport heights during the LGM compared to PI as a con- sequence of reduced convection due to colder surfaces, indi- cating a vertically less extensive Polar cell
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