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Data refer to export fluxes of carbonate produced by calcifying phytoplankton (coccolithophores), and coccolith-CaCO₃ percent contribution to total carbonate flux across the tropical North Atlantic, from upwelling affected NW Africa, via three ocean sites along 12°N to the Caribbean. Sampling was undertaken by means of a spatial array of four time-series sediment traps (i.e., CB at 21°N 20°W; M1U at 12°N 23°W; M2U at 14°N 37°W; M4U at 12°N 49°W; Guerreiro et al., 2021) collecting particle fluxes in two-week intervals, from October 2012 to February 2014, allowing to track temporal changes along the southern margin of the North Atlantic central gyre. Auxiliary PIC (Particulate Inorganic Carbon) data from NASA's Ocean Biology Processing Group (https://oceancolor.gsfc.nasa.gov) are also provided for the sediment sampling period at all four trap sites. Particle flux data (mg/m²/d) of CaCO₃, organic matter, particulate organic carbon (POC), biogenic silica (bSiO₂) and unspecified residual fraction are provided for sediment trap site CB.

In this study we analyzed sediment trap time series from five tropical sites to assess seasonal variations in concentrations and fluxes of long-chain diols (LCDs) and associated proxies with emphasis on the long-chain diol index (LDI) temperature proxy. For the tropical Atlantic, we observe that generally less than 2 % of LCDs settling from the water column are preserved in the sediment. The Atlantic and Mozambique Channel traps reveal minimal seasonal variations in the LDI, similar to the two other lipid-based temperature proxies TEX86 and U37K′. In addition, annual mean LDI-derived temperatures are in good agreement with the annual mean satellite-derived sea surface temperatures (SSTs). In contrast, the LDI in the Cariaco Basin shows larger seasonal variation, as do the TEX86 and U37K′. Here, the LDI underestimates SST during the warmest months, which is possibly due to summer stratification and the habitat depth of the diol producers deepening to around 20–30 m. Surface sediment LDI temperatures in the Atlantic and Mozambique Channel compare well with the average LDI-derived temperatures from the overlying sediment traps, as well as with decadal annual mean SST. Lastly, we observed large seasonal variations in the diol index, as an indicator of upwelling conditions, at three sites: in the eastern Atlantic, potentially linked to Guinea Dome upwelling; in the Cariaco Basin, likely caused by seasonal upwelling; and in the Mozambique Channel, where diol index variations may be driven by upwelling from favorable winds and/or eddy migration.

Long chain n-alkanes are terrestrial higher plant biomarkers used to reconstruct continental paleoclimatic and paleohydrological conditions with marine sedimentary archives. Latitudinal variation in their concentration and distribution in marine sediments relatively close to the continent has been widely studied, but little is known on how far this continental signal extends into the ocean. Furthermore, no studies have examined the seasonal variation in the deposition of these biomarkers in marine sediments. Here we studied longitudinal variation in the composition of long chain n-alkanes and two other terrestrial higher plant biomarkers (long chain n-alkanols and long chain fatty acids) in atmospheric particles, as well as longitudinal and seasonal variation in long chain n-alkanes in sinking particles in the ocean at different water depths and in surface sediments, all collected along a 12°N transect across the tropical North Atlantic Ocean. The highest abundance of all three biomarker classes was closest to the African coast, as expected, because they are transported with Saharan dust and the largest part of the dust is deposited close to the source. At this proximal location, the seasonal variability in long chain n-alkane flux and the chain length distribution of the n-alkanes in sinking particles was most pronounced, due to seasonal change in the dust source or due to change in vegetation composition in the source area, related to the position of the Intertropical Convergence Zone (ITCZ). In contrast, in the open ocean the seasonal variability in both the long chain n-alkane flux and chain length distribution of the n-alkanes was low. The abundance of the alkanes was also lower, as expected because of the larger source-to-sink distance. At the western part of the transect, close to South America, we found an additional source of the alkanes in the sinking particles during spring and autumn in the year 2013. The d13C of the alkanes in the surface sediment closest to the South American continent indicated that the isotope signal is likely derived from C3 vegetation from the Amazon, implying an input from the Amazon River, as there is no significant aeolian input from South America there since the prevailing wind direction is from the east. Finally, the concentration of the alkanes was similar in the material collected from the atmosphere, the particles collected while settling through the marine water column, and in the surface sediments, providing evidence that degradation of long chain n-alkanes from the atmosphere to settling at the sediment-water interface at deep open ocean sites is minimal.

In this study we have analyzed sediment trap time series from five tropical sites to assess seasonal variations in concentrations and fluxes of long-chain diols (LCDs) and associated proxies with emphasis on the Long chain Diol Index (LDI). For the tropical Atlantic, we observe that generally less than 2 % of LCDs settling from the water column are preserved in the sediment. The Atlantic and Mozambique Channel traps reveal minimal seasonal variations in the LDI, similar to the TEX86 and UK´37. However, annual mean LDI-derived temperatures are in good agreement with the annual mean satellite-derived sea surface temperatures (SSTs). In the Cariaco Basin the LDI shows larger seasonal variation, as do the TEX86 and UK´37. Here, the LDI underestimates SST during the warmest months, which is likely due to summer stratification and the habitat depth of the diol producers deepening to around 20 to 30 m. Surface sediment LDI temperatures in the Atlantic and Mozambique Channel compare well with the average LDI-derived temperatures from the overlying sediment traps, as well as with decadal annual mean SST. Lastly, we observed large seasonal variations in the Diol Index, as indicator of upwelling conditions, at three sites, potentially linked to Guinea Dome upwelling (Eastern Atlantic), seasonal upwelling (Cariaco Basin) and seasonal upwelling and/or eddy migration (Mozambique Channel).

The Eastern Mediterranean Transient (EMT) occurred in the Aegean Sea from 1988 to 1995 and is the most significant intermediate-to-deep Mediterranean overturning perturbation reported by instrumental records. The EMT was likely caused by accumulation of high salinity waters in the Levantine and enhanced heat loss in the Aegean Sea, coupled with surface water freshening in the Sicily Channel. It is still unknown whether similar transients occurred in the past and, if so, what their forcing processes were. In this study, sediments from the Sicily Channel document surface water freshening (SCFR) at 1910±12, 1812±18, 1725±25 and 1580±30 CE. A regional ocean hindcast links SCFR to enhanced deep-water production and in turn to strengthened Mediterranean thermohaline circulation. Independent evidence collected in the Aegean Sea supports this reconstruction, showing that enhanced bottom water ventilation in the Eastern Mediterranean was associated with each SCFR event. Comparison between the records and multi-decadal atmospheric circulation patterns and climatic external forcings indicates that Mediterranean circulation destabilisation occurs during positive North Atlantic Oscillation (NAO) and negative Atlantic Multidecadal Oscillation (AMO) phases, reduced solar activity and strong tropical volcanic eruptions. They may have recurrently produced favourable deep-water formation conditions, both increasing salinity and reducing temperature on multi-decadal time scales.

Mineral dust has a large impact on regional and global climate, depending on its particle size. Especially in the Atlantic Ocean downwind of the Sahara, the largest dust source on earth, the effects can be substantial but are poorly understood. This study focuses on seasonal and spatial variations in particle size of Saharan dust deposition across the Atlantic Ocean, using an array of submarine sediment traps moored along a transect at 12° N. We show that the particle size decreases downwind with increased distance from the Saharan source, due to higher gravitational settling velocities of coarse particles in the atmosphere. Modal grain sizes vary between 4 and 33 µm throughout the different seasons and at five locations along the transect. This is much coarser than previously suggested and incorporated into climate models. In addition, seasonal changes are prominent, with coarser dust in summer, and finer dust in winter and spring. Such seasonal changes are caused by transport at higher altitudes and at greater wind velocities during summer than in winter. Also the latitudinal migration of the dust cloud, associated with the Intertropical Convergence Zone, causes seasonal differences in deposition as the summer dust cloud is located more to the north, and more directly above the sampled transect. Furthermore, increased precipitation and more frequent dust storms in summer coincide with coarser dust deposition. Our findings contribute to understanding Saharan dust transport and deposition relevant for the interpretation of sedimentary records for climate reconstructions, as well as for global and regional models for improved prediction of future climate.