Search for: All records

Aerosol radiative forcing is an important but often poorly understood component of regional climate. While glacier ice contains the most detailed archives of past atmospheric aerosol composition and temperature, no well-preserved ice records extending into the last climatic transition have been reported for the historically important European region. Here, we use an Alpine ice core to document changes in European aerosols and climate from the end of the last glacial age (LGA) through the Holocene. The core was drilled on a glacier dome in the French Alps called the Dôme du Goûter (DDG), and it provides a stratigraphically intact record of aerosol and climate extending to at least 12 kyears (ky) before present. Although dating near the base of the glacier is not well constrained, the oldest DDG ice layers reflect glacial conditions in western Europe during the LGA. In addition to changes in atmospheric transport, increased sea-salt and dust deposition in western Europe recorded in the LGA ice suggest enhanced westerly winds and more active dust sources, possibly including North Africa. Deposition of terrestrial biogenic indicators during the cold LGA climate was lower, however, consistent with strongly reduced European vegetation. The DDG record of terrestrial biogenic emissions also suggests a decline of European forests throughout the Holocene, resulting from deterioration of climatic conditions and more recently from establishment of the first agricultural societies. The pronounced changes in atmospheric aerosol recorded in Alpine ice imply large variations in aerosol radiative forcing in western Europe during the last 12 ky. 

Abstract Iron emissions from human activities, such as oil combustion and smelting, affect the Earth's climate and marine ecosystems. These emissions are difficult to quantify accurately due to a lack of observations, particularly in remote ocean regions. In this study, we used long‐term, near‐source observations in areas with a dominance of anthropogenic iron emissions in various parts of the world to better estimate the total amount of anthropogenic iron emissions. We also used a statistical source apportionment method to identify the anthropogenic components and their sub‐sources from bulk aerosol observations in the United States. We find that the estimates of anthropogenic iron emissions are within a factor of 3 in most regions compared to previous inventory estimates. Under‐ or overestimation varied by region and depended on the number of sites, interannual variability, and the statistical filter choice. Smelting‐related iron emissions are overestimated by a factor of 1.5 in East Asia compared to previous estimates. More long‐term iron observations and the consideration of the influence of dust and wildfires could help reduce the uncertainty in anthropogenic iron emissions estimates.