Elsevier

Atmospheric Environment

Volume 41, Issue 31, October 2007, Pages 6497-6509
Atmospheric Environment

Effect of local and long-range transport emissions on the elemental composition of PM10–2.5 and PM2.5 in Beirut

https://doi.org/10.1016/j.atmosenv.2007.04.032Get rights and content

Abstract

The elemental composition of PM10−2.5 and PM2.5 were studied in winter, summer, stormy and non-stormy dates during a period extending from February 2004 till January 2005, in a populated area of Beirut. Results of PIXE analysis and enrichment factor (E.F.) calculation, using Si as a reference of crustal material, showed that crustal elements (E.F.<10) like Si, Ca, K, Ti, Mn and Fe were more abundant in PM10−2.5 while enriched elements (E.F.>10) like S, Cu, Zn and Pb predominated in PM2.5. In PM10−2.5, concentrations of crustal elements increased during stormy episodes, all time high Ca concentrations were due to the abundance of calcite and limestone rocks in Lebanon, and increased Cl levels correlated with marine air masses. In PM2.5, sulfur concentrations were more prominent in the summer due to the enhancement of photochemical reactions. Sources of sulfur were attributed to local, sea-water and long-range transport from Eastern Europe, with the latter being the most predominate. Anthropogenic elements like Cu and Zn were generated from worn brakes and tires in high traffic density area and spikes of Pb were directly linked to a southerly wind originated from Egypt and/or Israel as determined by the air trajectory HYSPLIT model. In brief, elemental variations depended on the regional variability of the transport pattern and the different removal rates of aerosols.

Introduction

The Mediterranean basin is considered one of the most controversial regions for aerosol transportation due to its location at the intersection of air masses circulating among the three continents (Lelieveld et al., 2002). It is situated just North of the Saharan Desert of Africa, and South of the heavily populated and highly industrialized European continent. Other studies conducted in the North-Western (Spain, France, Italy) (Bergametti et al., 1989; Chester et al., 1999; Dulac et al., 1987; Migon et al., 1991; Querol et al., 2001; Sandroni and Migon, 1997) and eastern (Greece, Turkey, Israel) Mediterranean regions (Chabas and Lefevre, 2000; Erduran and Tuncel, 2001; Erel et al., 2006; Ganor et al., 1991; Graham et al., 2004; Gullu et al., 2000; Maenhaut et al., 1999; Mamane et al., 1980; Manalis et al., 2005; Manoli et al., 2002; Mihalopoulos et al., 1997; Thomaidis et al., 2003; Vousta et al., 2002; Yatin et al., 2000) emphasized the diversity of the atmosphere over the Mediterranean basin. In Lebanon, seasonal dust storms coming from the Arabian (South-East) and Saharan Deserts (South-West) in the Fall and Spring mild seasons, constitute the major source of mineral elements (Kubilay et al., 2000). Long-range transport of pollutants coming from central Europe enrich the air with sulfur dioxide (SO2) (Ganor et al., 2000; Luria et al., 1996; Sciare et al., 2003; Tsitouridou et al., 2003; Zerefos et al., 2000), whereas marine aerosols contribute to sea-salt aerosols. Moreover, local emission cause an increase in the levels of nitrate and sulfate aerosols derived from oxides of nitrogen and SO2, respectively (Danalatos and Glavas, 1999; Erduran and Tuncel, 2001; Kassomenos et al., 1999). Sulfur (S) concentration increases in the hot and humid summer (June, July and August) due to the enhancement of photochemical oxidation of SO2, and drops in the rainy winter (December, January, and February) (Kouyoumdjian and Saliba, 2006). The purpose of this study was to determine the elemental content of PM10–2.5 and PM2.5 in Beirut during selected days in winter, summer, stormy and non-stormy episodes, using the particulate-induced X-ray emission (PIXE) technique. Also, a comparison between the elemental composition of the two particle sizes and the source apportionment through elemental–meteorological correlations are established.

Section snippets

Sampling

The sampling was conducted in one of the busiest areas of Beirut; Bourj Hammoud (33°53′N, 35°32′E) (Fig. 1) located in the North-Eastern suburb of Beirut at about 1 km away from the Mediterranean coast at an elevation of less than 10 m above sea level. This site is characterized by a high density of residential and commercial premises, and a very high volume of vehicular traffic. It also experiences a high volume of sea-spray, exhausts from Beirut harbor operations and some waste-mass burning

Results and discussion

The mass concentrations of PM10–2.5 and PM2.5 and their corresponding elemental composition (Si, S, Cl, K, Ca, Ti, Mn, Fe, Cu, Zn, and Pb) are presented in Table 2. Other elements such as V, Cr, Co, Ni, Cd, As, Se and Br were found to be below the limit of detection. Ca, Si and Fe prevailed in the PM10–2.5 samples forming an average of 17% of the total mass average. In PM2.5, this percentage decreased to 3%, while S; the most abundant element, constituted almost 4.6% of the average mass

Conclusions

Elemental analysis of PM10–2.5 and PM2.5 particles using PIXE analysis showed the presence of Si, S, Cl, K, Ca, Ti, Mn, Fe, Cu, Zn, and Pb. Based on the E.F. calculation, the crustal elements were defined as Si, K, Ti, Mn, Ca and Fe while the rest were classified as non-crustal. Their distribution between PM10–2.5 and PM2.5 and their source apportionment were as follows:

  • Elevated concentrations of crustal elements, mostly present in PM10–2.5, were associated with desert storms coming from the

Acknowledgements

This study was supported by the University Research Board (URB) at the American University of Beirut. The authors would like to thank the California Air resources Board, specifically Dr. Bart Croes, for the donation of the virtual impactor. A special thank is also extended to the municipality of Bourj Hammoud, especially (Mrs. Arpiné Mangasarian), for their great cooperation and help, and the NOAA Laboratory for making HYSPLIT model available to researchers all over the world.

References (44)

  • N. Kubilay et al.

    An illustration of the transport and deposition of mineral dust onto the Eastern Mediterranean

    Atmospheric Environment

    (2000)
  • G. Lonati et al.

    Major chemical components of PM2.5 in Milan (Italy)

    Atmospheric Environment

    (2005)
  • W. Maenhaut et al.

    Detailed mass size distributions of atmospheric aerosol species in the Negev Desert, Israel, during ARACHNE-96

    Nuclear Instruments & Methods B

    (1999)
  • N. Manalis et al.

    Toxic metal content of particulate matter (PM10), within the Greater Area of Athens

    Chemosphere

    (2005)
  • E. Manoli et al.

    Chemical characterization and source identification/apportionment of fine and coarse air particles in Thessaloniki, Greece

    Atmospheric Environment

    (2002)
  • J.A. Maxwell et al.

    The Guelph PIXE software

    Nuclear Instruments & Methods in Physics Research Section B

    (1989)
  • C. Migon et al.

    Evolution of total atmospheric deposition of Pb, Cd, Cu and Zn to the Ligurian Sea

    Science of Total Environment

    (1991)
  • X. Querol et al.

    PM10 and PM2.5 source apportionment in the Barcelona Metropolitan area, Catalonia, Spain

    Atmospheric Environment

    (2001)
  • V. Sandroni et al.

    Significance of trace metal medium range transport in the Western Mediterranean

    Science of Total Environment

    (1997)
  • H. Shaka’ et al.

    Concentration measurements and chemical composition of PM10–2.5 and PM2.5 at a coastal site in Beirut, Lebanon

    Atmospheric Environment

    (2004)
  • N.S. Thomaidis et al.

    Characterization of lead, cadmium, arsenic and nickel in PM2.5 particles in the Athens atmosphere, Greece

    Chemosphere

    (2003)
  • K. Torfs et al.

    Chemical relations between atmospheric aerosols, deposition and stone decay layers on historic buildings at the Mediterranean coast

    Atmospheric Environment

    (1997)
  • Cited by (70)

    • Comprehensive chemical characterization of PM<inf>2.5</inf> in the large East Mediterranean-Middle East city of Beirut, Lebanon

      2023, Journal of Environmental Sciences (China)
      Citation Excerpt :

      High PM2.5 concentrations were recorded between the 3rd and the 6th of May, where the concentration of fine particles reached 99 and 129 μg/m3 at USJ and Hersh, respectively. Lebanon experiences seasonal dust storms coming from the Arabian and Saharan Deserts in the fall and spring seasons, respectively (Saliba et al., 2007). FLEXPART retroplumes showed that air masses in Beirut during this period were transported from North Africa (Fig. 2), which could explain the high PM2.5 and mineral dust concentrations for these days.

    • Chemical characteristics of PM<inf>2.5-0.3</inf> and PM<inf>0.3</inf> and consequence of a dust storm episode at an urban site in Lebanon

      2016, Atmospheric Research
      Citation Excerpt :

      Taking together with the back-trajectories, it could suggest that the dust storm had directly influenced the beginning of the first sampling period, and then indirectly influenced the rest of the sampling campaign by the re-suspension of deposited dust particles in dry weather conditions throughout the study period. It is well known that Lebanon is subjected to seasonal dust storms coming from the Arabian (South-East) and Saharan Deserts (South-West) in the fall and spring mild seasons (Dada et al., 2013; Jaafar et al., 2014; Saliba et al., 2007). In addition, many studies conducted in the Mediterranean region (Alastuey et al., 2005; Balis et al., 2004; De Tomas et al., 2003; Griffin et al., 2007; Kandler et al., 2007; Remoundaki et al., 2011) and other regions such as over the Atlantic (Aarons et al., 2013), in Ireland (Dall'Osto et al., 2010), in Germany (Flentje et al., 2015), in Switzerland (Schwikowski et al., 1995) and Hungary (Szoboszlai et al., 2009) were focused on Saharan dust storms because the Sahara produces more aeolian soil dusts than any other world desert (Aydin et al., 2012) and this can be transported by wind over long distances (Szoboszlai et al., 2009).

    • Evaluation and mapping of PM<inf>2.5</inf> atmospheric aerosols in Arasia region using PIXE and gravimetric measurements

      2016, Nuclear Instruments and Methods in Physics Research, Section B: Beam Interactions with Materials and Atoms
    View all citing articles on Scopus
    View full text