The Air-Sea Exchange of Particulate Organic Matter: The Sources and Long-Range Transport of Lipids in Aerosols

This review focuses on the long-range atmospheric transport of metals to organic-rich surface soils (mostly 50–90% organic matter) in the temperate, coniferous, and boreal zones of North America and Europe. From various air-pollution related measurements (air, precipitation, moss, peat cores) Pb and Zn are known to be transported long distances in the air in large amounts. Arsenic, Cd, Hg, Sb, and Se are also typical representatives of long-range transported air masses, and there is evidence that Ag, Bi, In, Mo, Tl, and W belong to this group of elements. Through the use of “environmental archives” such as ice and peat cores it has become evident that long-range transport of pollutants and associated contamination of natural surfaces is not just a recent phenomenon. There is compelling evidence for widespread enrichment of surface soil horizons in Pb from long-range transport, and many studies support enrichment of Zn. Mercury is also generally elevated by anthropogenic emissions over natural levels in organic-rich surface soils, whereas results for Cd are less conclusive. There is evidence that As, Se, Ag, Mo, In, Sb, W, Tl, and Bi all are subject to some enrichment in organic-rich surface soils from long-range atmospheric transport, but studies are still few for most of these elements. With the exception of Pb, little is known about residence times of the elements in the organic-rich surface horizon, and more research is needed on this topic. Further studies are desirable on the temporal and spatial trends in supply of the above elements, which are poorly known in large parts of the northern temperate zone.Key words: natural soils, metals, long-range atmospheric transport, organic matter, lead, zinc, cadmium, mercury.

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Long-term measurements of carbonaceous aerosols in the Eastern Mediterranean: evidence of long-range transport of biomass burning

Atmospheric Chemistry and Physics ◽

10.5194/acp-8-5551-2008 ◽

2008 ◽

Vol 8 (18) ◽

pp. 5551-5563 ◽

Cited By ~ 126

Author(s):

J. Sciare ◽

K. Oikonomou ◽

O. Favez ◽

E. Liakakou ◽

Z. Markaki ◽

...

Keyword(s):

Organic Matter ◽

Organic Carbon ◽

Long Range ◽

Biomass Burning ◽

Water Soluble ◽

Long Range Transport ◽

Crete Island ◽

Yearly Average ◽

Range Transport

Abstract. Long-term (5-year) measurements of Elemental Carbon (EC) and Organic Carbon (OC) in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island). A multi-analytical approach (including thermal, optical, and thermo-optical techniques) was applied for these EC and OC measurements. Light absorbing dust aerosols were shown to poorly contribute (+12% on a yearly average) to light absorption coefficient (babs) measurements performed by an optical method (aethalometer). Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March–April and July–September). The contribution of biomass burning to the concentrations of EC and OC was shown to be rather small (20 and 14%, respectively, on a yearly basis), although this contribution could be much higher on a monthly basis and showed important seasonal and interannual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC) have shown that the monthly mean WSOC/OC ratio remains stable throughout the year (0.45±0.12), suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA) formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A.D.<1.5μm) showed that the mass contribution of organic matter (POM) was found to be essentially invariable during the year (monthly average of 26±5%).

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Long-term measurements of carbonaceous aerosols in the eastern Mediterranean: evidence of long-range transport of biomass burning

Atmospheric Chemistry and Physics Discussions ◽

10.5194/acpd-8-6949-2008 ◽

2008 ◽

Vol 8 (2) ◽

pp. 6949-6982 ◽

Cited By ~ 4

Author(s):

J. Sciare ◽

K. Oikonomou ◽

O. Favez ◽

Z. Markaki ◽

E. Liakakou ◽

...

Keyword(s):

Organic Matter ◽

Organic Carbon ◽

Long Range ◽

Biomass Burning ◽

Water Soluble ◽

Long Range Transport ◽

Crete Island ◽

Yearly Average ◽

Range Transport

Abstract. Long-term (5-yr) measurements of Black Carbon (BC) and Organic Carbon (OC) in bulk aerosols are presented here for the first time in the Mediterranean Basin (Crete Island). A multi-analytical approach (including thermal, optical, and thermo-optical techniques) was applied for these BC and OC measurements. Light absorbing dust aerosols have shown to poorly contribute (+17% on a yearly average) to light absorption coefficient (babs) measurements performed by an optical method (aethalometer). Long-range transport of agricultural waste burning from European countries surrounding the Black Sea was shown for each year during two periods (March–April and July–September). The contribution of biomass burning to the concentrations of BC and OC has shown to be rather small (20 and 14%, respectively, on a yearly basis), although this contribution could be much higher on a monthly basis and is expected a high intra and inter annual variability. By removing the biomass burning influence, our data revealed an important seasonal variation of OC, with an increase by almost a factor of two for the Spring months of May and June, whereas BC was found to be quite stable throughout the year. Preliminary measurements of Water Soluble Organic Carbon (WSOC) have shown that the monthly mean WSOC/OC ratio remains stable throughout the year (0.45±0.12), suggesting that the partitioning between water soluble and water insoluble organic matter is not significantly affected by biomass burning and secondary organic aerosol (SOA) formation. A chemical mass closure performed in the fine mode (Aerodynamic Diameter, A.D.<1.5 μm) showed that the mass contribution of organic matter (POM) was found to be essentially invariable during the year (monthly average of 26±5%).

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Joint analysis of continental and regional background environments in the western Mediterranean: PM<sub>1</sub> and PM<sub>10</sub> concentrations and composition

Atmospheric Chemistry and Physics ◽

10.5194/acp-15-1129-2015 ◽

2015 ◽

Vol 15 (2) ◽

pp. 1129-1145 ◽

Cited By ~ 19

Author(s):

A. Ripoll ◽

M. C. Minguillón ◽

J. Pey ◽

N. Pérez ◽

X. Querol ◽

...

Keyword(s):

Organic Matter ◽

Chemical Composition ◽

Long Range ◽

Western Mediterranean ◽

Anthropogenic Sources ◽

Long Range Transport ◽

Background Site ◽

Regional Background ◽

Range Transport ◽

Dust Resuspension

Abstract. The complete chemical composition of atmospheric particulate matter (PM1 and PM10) from a continental (Montsec, MSC, 1570 m a.s.l.) and a regional (Montseny, MSY, 720 m a.s.l) background site in the western Mediterranean Basin (WMB) were jointly studied for the first time over a relatively long-term period (January 2010–March 2013). Differences in average PMX concentration and composition between both sites were attributed to distance to anthropogenic sources, altitude, and different influence of atmospheric episodes. All these factors result in a continental-to-regional background increase of 4.0 μg m−3 for PM10 and 1.1 μg m−3 for PM1 in the WMB. This increase is mainly constituted by organic matter, sulfate, nitrate, and sea salt. However, higher mineral matter concentrations were measured at the continental background site owing to the higher influence of long-range transport of dust and dust resuspension. Seasonal variations of aerosol chemical components were attributed to evolution of the planetary boundary layer (PBL) height throughout the year, variations in the air mass origin, and differences in meteorology. During warmer months, weak pressure gradients and elevated insolation generate recirculation of air masses and enhance the development of the PBL, causing the aging of aerosols and incrementing pollutant concentrations over a large area in the WMB, including the continental background. This is reflected in a more similar relative composition and absolute concentrations of continental and regional background aerosols. Nevertheless, during colder months the thermal inversions and the lower vertical development of the PBL leave MSC in the free troposphere most of the time, whereas MSY is more influenced by regional pollutants accumulated under winter anticyclonic conditions. This results in much lower concentrations of PMX components at the continental background site with respect to those at the regional background site. The influence of certain atmospheric episodes caused different impacts at regional and continental scales. When long-range transport from central and eastern Europe and from north Africa occurs, the continental background site is frequently more influenced, thus indicating a preferential transport of pollutants at high altitude layers. Conversely, the regional background site was more influenced by regional processes. Continental and regional aerosol chemical composition from the WMB revealed (a) high relevance of African dust transport and regional dust resuspension; (b) low biomass burning contribution; (c) high organic matter contribution; (d) low summer nitrate concentrations; and (e) high aerosol homogenization in summer.

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