USGS Science⌕ Search
Home/Archive/USGS

USGS · 70102295

A radiogenic isotope tracer study of transatlantic dust transport from Africa to the Caribbean

A. Kumar·W. Abouchami·S.J.G. Galer·V.H. Garrison·E. Williams·M.O. Andreae
View original source ↗Export metadata ↓

Abstract

Many studies have suggested that long-range transport of African desert dusts across the Atlantic Ocean occurs, delivering key nutrients and contributing to fertilization of the Amazon rainforest. Here we utilize radiogenic isotope tracers – Sr, Nd and Pb – to derive the provenance, local or remote, and pathways of dust transport from Africa to the Caribbean. Atmospheric total suspended particulate (TSP) matter was collected in 2008 on quartz fibre filters, from both sides of the Atlantic Ocean at three different locations: in Mali (12.6°N, 8.0°W; 555 m a.s.l.), Tobago (11.3°N, 60.5°W; 329 m a.s.l.) and the U.S. Virgin Islands (17.7°N, 64.6°W; 27 m a.s.l.). Both the labile phase, representative of the anthropogenic signal, and the refractory detrital silicate fraction were analysed. Dust deposits and soils from around the sampling sites were measured as well to assess the potential contribution from local sources to the mineral dust collected. The contribution from anthropogenic sources of Pb was predominant in the labile, leachate phase. The overall similarity in Pb isotope signatures found in the leachates is attributed to a common African source of anthropogenic Pb, with minor inputs from other sources, such as from Central and South America. The Pb, Sr and Nd isotopic compositions in the silicate fraction were found to be systematically more radiogenic than those in the corresponding labile phases. In contrast, Nd and Sr isotopic compositions from Mali, Tobago, and the Virgin Islands are virtually identical in both leachates and residues. Comparison with existing literature data on Saharan and Sahelian sources constrains the origin of summer dust transported to the Caribbean to mainly originate from the Sahel region, with some contribution from northern Saharan sources. The source regions derived from the isotope data are consistent with 7-day back-trajectory analyses, demonstrating the usefulness of radiogenic isotopes in tracing dust provenance and atmospheric transport.

Explore related subjects

Atmospheric EnvironmentArticle
90° N90° S · 180° W ← longitude → 180° E
Source-reported bounding extent: -20° to 40° latitude; -80° to 45° longitude. This indicates report coverage, not an exact sampling location. View area on OpenStreetMap.

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

A. Kumar, W. Abouchami, S.J.G. Galer, V.H. Garrison, E. Williams, M.O. Andreae. 2014. A radiogenic isotope tracer study of transatlantic dust transport from Africa to the Caribbean. https://doi.org/10.1016/j.atmosenv.2013.10.021

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related USGS reports

USGS2021

Trends in precipitation chemistry across the U.S. 1985–2017: Quantifying the benefits from 30 years of Clean Air Act amendment regulation

Acid rain was first recognized in the 1970s in North America and Europe as an atmospheric pollutant that was causing harm to ecosystems. In response, the U.S. Congress enacted Title IV of the Clean Air Act Amendments (CAA) in 1990 to reduce sulfur and nitrogen emissions from fossil fuel burning power plants. This study reports trends in wet-precipitation chemistry in response to emissions reductions implemented as part of the CAA. Trends were calculated for sulfate (SO 4 ), nitrate (NO 3 ) and ammonium (NH 4 ) from 1985 to 2017 at 168 stations operated by the National Atmospheric Deposition Program (NADP); stations were divided into 9 regions across the United States. Trend analyses were conducted for three time periods: Period 1 (1985–1999), Period 2 (2000–2017), and the entire study period (1985–2017). Seasonal and regional Kendall trend analyses reveal significant decreasing trends in mean wet-precipitation SO 4 concentrations in all 9 regions during the entire study period. The largest decreasing trends in monthly mean SO 4 precipitation-weighted concentrations were measured in the Mid-Atlantic (−1.29 μeq/l/yr), Midwest (−1.15 μeq/l/yr), and Northeast regions (−1.10 μeq/l/yr). The trends in monthly mean NO 3 concentrations were not as strong as those for SO 4 , but all of the regions had significant decreasing trends in NO 3 and again the Mid-Atlantic (−0.53 μeq/l/yr), Midwest (−0.44 μeq/l/yr), and Northeast regions (−0.50 μeq/l/yr) had the strongest trends. Trends were steepest during Period 2 for SO 4 and NO 3 , in fact for NO 3 86% of the stations had significant decreasing trends during Period 2 while only 8% of the stations had significant decreasing trends during Period 1. The stations with the highest concentrations of SO 4 and NO 3 at the beginning of the study had the strongest decreasing trends and the relations were stronger during Period 2 than Period 1. For NH 4 , 22% of the stations had statistically significant increasing trends in concentration during Period 1. The largest increasing trends in wet-precipitation NH 4 concentration occurred in the North-Central region during Period 1, Period 2 and throughout the entire study. By comparison, NH 4 trends in the Rocky-North and Rocky-South regions were about half as steep and trends in the South-Central and Midwest regions were about one-third as steep. We compared trends in SO 4 and NO 3 concentrations from NADP stations to emissions of sulfur dioxide and nitrogen oxides, respectively to determine whether there was a relation between emissions and wet-precipitation concentration trends within proximity to NADP stations. There was a statistically significant relation (r 2 = 0.62–0.69, p < 0.01) between the trend in SO 4 concentrations at individual NADP stations and total and mean sulfur dioxide (SO 2 ) emissions from power plants within a range of 750 km and 1000 km from each station. There were also significant relations between NO 3 concentration trends at NADP stations and power plant emissions of nitrogen oxides, but they were not nearly as strong (r 2 = 0.18–0.36, p < 0.01) as those for SO 4 and were strongest for emissions within a range of 1000 km and 1500 km from each NADP station. Decreases in wet-precipitation SO 4 concentrations were more consistent across regions and through time than decreases in NO 3 and SO 4 trends were more closely linked to stationary emissions sources than NO 3 trends. There were statistically significant increases in NH 4 wet-precipitation concentrations, as have been reported in previous studies, but this study found that those increases were strongest during Period 1 and were not consistent across the United States. During the first 3 years of the study period, wet-precipitation acidity was dominated by SO 4 in 8 of the 9 regions; by 2017 NO 3 dominated the acidity of wet-precipitation in 7 of the 9 regions. There has also been a downward shift in the NO 3 :NH 4 ratio of wet-precipitation as the emissions of nitrogen oxides have declined while ammonia emissions have remained essentially constant. This shift has resulted in an increase in wet-precipitation total nitrogen concentrations in 7 of the 9 regions and indicate that efforts to control NH 3 emissions will become increasingly important as emissions of nitrogen oxides continue to decline.

Atmospheric Environment↗
USGS2021

Trends and current status of aluminum chemistry in Adirondack headwater streams 30 Years after the Clean Air Act Amendments of 1990

Mobilization of toxic forms of aluminum (Ali) have been one of the most harmful effects of acidic deposition on aquatic ecosystems. Large decreases in acidic deposition levels have resulted in decreases in Ali concentrations in surface waters starting in the 1990s. However, recent studies indicate that fish communities are still being impaired by elevated Ali concentrations in streams, suggesting the need for a present-day assessment of the recovery status of Al chemistry in impacted regions such as the Adirondack region of New York, United States. Therefore, the recovery status of Al was assessed from long-term high-frequency monitoring of three Adirondack streams up through 2019, and multiple resampling of 127 headwater streams throughout the Adirondack region between 2004/2005 and 2018/2019. Results indicated that concentrations of Ali have continued to decrease throughout the Adirondack region, but that harmful conditions still exist in a substantial number of streams during spring snowmelt. In the western Adirondack region, 35 percent of streams during spring snowmelt, (typically the most acidic period), and 10 percent of streams during summer were still experiencing harmful concentrations of Ali ( >1.0 μmol L −1 ) in 2018/2019. In the less-impacted east-central Adirondack region, 10 percent of streams during snowmelt, and 4 percent of streams during summer were experiencing harmful Ali concentrations in 2018. Temporal decreases in Ali concentrations were due in part to a shift in speciation from Ali to non-toxic organically complexed Al as dissolved organic carbon concentrations increased, which was also a response to decreasing acidic deposition. Increased availability of calcium resulting from acid-neutralization processes such as weathering also contributed to the decrease in Ali over the past 5–8 years. The current low levels of acidic deposition may have begun to enhance recovery by increasing the effectiveness of ambient acid neutralization processes.

New York↗
USGS2021

Biological and chemical recovery of acidified Catskill Mountain streams in response to the Clean Air Act Amendments of 1990

Decades of acidic deposition have adversely affected aquatic and terrestrial ecosystems in acid-sensitive watersheds in parts of the eastern United States. The national Acid Rain Program (Title IV of the 1990 Clean Air Act Amendments - CAAA) helped reduce emissions of sulfur dioxide (SO 2 ) and nitrogen oxides (NO x ) and resulted in sharp decreases in the acidity of atmospheric deposition. The decrease in acidic deposition produced a steady decline in the acidity of streams in many poorly buffered waters across the western Adirondacks and parts of the Catskill Mountains of New York. Until recently, however, there has been little evidence of biological recovery in most acid-sensitive streams in both regions. Long-term deposition and stream-chemistry records and fish-community data from quantitative surveys done during 1991–93 and again during 2012–19 at 13 sites in the upper Neversink River and its tributaries were evaluated to determine if chemical and biological recovery were evident in this Catskill Mountain watershed and if they could be linked to regional declines in acidic deposition. Between 1991 and 2019, large decreases in sulfate and nitrate deposition in the basin mirrored declines in total nationwide SO 2 and NO x emissions. There were corresponding decreases in sulfate and nitrate concentrations in deposition at a National Trends Network station at Frost Valley (NY68) and coincident declines in sulfate concentrations at four long-term monitoring sites in the Neversink River watershed. Mean acid neutralizing capacity and pH increased and inorganic aluminum (Al i ) concentrations from routine summertime samples decreased significantly at most moderately to severely acidified sites between the two study periods. Richness, density, and biomass of fish communities increased at most sites, while the density and biomass of brook trout Salvelinus fontinalis populations increased at fewer sites that were undergoing chemical recovery. Although recovery is far from complete, trends in deposition chemistry, water quality, and fish assemblages in streams of the upper Neversink watershed indicate that the 1990 CAAA is having positive impacts on aquatic ecosystems in the Catskill Mountain region, New York.

New York↗