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Abstract This work evaluates glacial dust as a source of sediment, and associated iron (Fe), to the Fe‐limited Gulf of Alaska (GoA). A reanalysis of GoA sediment data, using rare earth elements and thorium as provenance tracers, suggests a flux to the ocean surface of Copper River (AK) glacial dust, and associated Fe, that is comparable to the flux of dust from Asia, at least 1,000 km from the narrow mountain valley glacial dust source area. This work suggests dust from Asia may not be the largest source of Fe to the GoA. Dust models fail to accurately simulate this glacial dust transport because their coarse resolution underestimates wind speeds, and the dust flux. This work suggests that glacial dust fluxes may have been important in the geologic past (e.g., the last glacial maximum) from locations where there was more extensive coverage by glaciers than at present. 

Abstract Re‐examination of previously published dissolved iron time‐series data from Ocean Station Papa in the central Gulf of Alaska (GoA) reveals 33%–70% increases in the dissolved iron inventories occurring between September and February of successive years, implying a source of Fe to this region during autumn or early winter. Because I can virtually rule out many possible iron sources at this time of year, I suggest Alaskan glacial dust is the likely iron source. Large plumes of such dust are known to be generated regularly in the autumn by anomalous offshore winds and channeled through mountain gaps, simultaneously from several locations spanning ∼1,000 km of the northern Gulf of Alaska coastline. Large dust flux events occur when below‐freezing, low‐humidity air temperatures persist for many days during the autumn. I suggest that existing state‐of‐the‐art global dust models fail to reproduce this Alaskan dust flux because the model spatial resolution is too coarse to resolve the high winds through the narrow mountain gaps that generate the dust. Future work that could help to confirm this Fe source to the central GoA includes time‐series profiles of iron concentrations, and ancillary information from sensor‐equipped profiling floats. If this mechanism of Fe supply to the central GoA were confirmed, it would imply this Alaskan dust is transported ≥1,100 km from the coast, more than twice as far as has been visually documented from satellite observations. 

The trace metal geochemistry of atmospheric dust and terrestrial surface particles were studied on the Qatar Peninsula from February 2014 to November 2015. We included samples of the mega dust-storm event on 01–02 April 2015. Atmospheric dust samples were collected using passive dust traps. Terrestrial surface deposits of recent dust accumulation and traffic particulate from roads were also sampled. All samples were total acid digested and analyzed for major and trace elements using ICP-OES analyzer. The concentration of thirteen elements (Ca, Mg, Ag, As, Cd, Cr, Cu, Mo, Ni, Se, Sn, Sr, Zn) were enriched in atmospheric dust samples, relative to upper continental crust (UCC). Calcium was especially enriched by up to 435% relative to UCC. About 33% of the total sample mass was CaCO3, reflecting the composition of surface rocks and soils in the source areas. Of the elements typically associated with anthropogenic activity, Ag, Ni, and Zn were most enriched relative to UCC, with enrichment factors (EF) of 182%, 233%, and 209%, respectively. Other metals, which normally reflect anthropogenic sources, including Pb and V, were not significantly enriched, with enrichment factors of 25% and 3%, respectively. Major elements (Al, Mn, Fe) were depleted (− 58%, − 35%, and − 5%, respectively) relative to UCC due to the large dilution effect of the enrichment of CaCO3. Back trajectories were determined at the date of sampling for each sample using the NOAA HYSPLIT model. These showed that the source of the dust particles was almost equally divided between northerly and southerly sources, except one sample, which appeared to originate from the west. More variability in particle source locations were observed during the winter months (October to March). Samples from the mega-dust storm were solubilized using an acetic acid-hydroxylamine hydrochloride leach procedure to obtain an upper estimate of the potential contribution of bioactive elements to surface seawater. The leach procedure solubilized a significant fraction of almost all elements. Ca was the element most affected (81% removed) because of the carbonate minerals present. Bioactive elements like Fe (25%) and P (58%) were also significantly solubilized. Because river input is so small to the Arabian Gulf, this solubilized fraction of dust is likely a major source of nutrients to surface seawater. Enrichment factors were also calculated with respect to the average composition of terrestrial surface deposits (TSD). Samples are not enriched significantly with respect to major components (EF < 2), with a depletion in Ca, K, Na in dust storm samples, reflecting a different origin. A significant enrichment of the same trace metals is evident in dust deposits and in traffic samples, but not in dust storms: Cu, Mo, Ni, Zn, possibly deriving from local atmospheric sources (traffic, industries). Samples with northern and southern origins were compared to see if the composition could be used to identify source. Only three elements were observed to be statistically different. Pb and Na were higher in samples from the south, while Cr was higher in those from the north.