This study was carried out between January and February 2013, at two sites in the city of Cuernavaca, México, using low-volume equipment. Fifteen Polycyclic aromatic hydrocarbons (PAHs), were identified by gas chromatography coupled with mass spectrometry. The total average concentration observed for PAHs was 24.0 ng·m −3 , with the high molecular weight compounds being the most abundant. The estimated equivalent concentration for Benzo (a) P (BaPE) was 4.05 ng·m −3 . Diagnostic ratios together with the principal components analysis (PCA) allowed for establishing coal burning and vehicle OPEN ACCESSAtmosphere 2015, 6 1260 emissions as being the main sources of these compounds in the area. The PAHs used to calculate this index account for 51% of the 15 PAHs identified, which probably involves a risk to the exposed population.

Polycyclic aromatic hydrocarbons (PAHs) are formed in natural processes during combustion of biomass (e.g., forest fires) and by anthropogenic activities at high temperatures. In according with the suggestion the major sources of PAHs in the environment. The main sources of PAHs come basically from heat and power generation (e.g., coal, gas, wood, and oil), industrial processes (e.g., coke production), refuse burning and vehicle emissions. Human exposure to airborne PAHs can result from these processes, as well as from emissions from other sources, such as cooking, smoking, and materials containing PAHs (e.g., petroleum products and fuels). The potential serious health effects resulting from acute and chronic human exposure to PAHs are of concern. For this reason, the identification and quantification of PAHs in airborne particles have been a real challenge, given the multiple impacts that these substances represent for human health. In the last decade, multiple technological developments have been implemented, ranging from sampling systems, extraction and analysis of these compounds with the aim of obtaining more accurate and reliable results. This chapter was prepared to describe and to assess the state of the art about the evolution and application of sampling, extraction and analysis methodologies for the determination of PAHs in airborne particles.

Atmospheric particles with an aerodynamic diameter less than or equal to 2.5 micrometers (PM2.5) were collected at two sites located in the urban area of the city of Cuernavaca (Morelos) during a season when a large number of forest fires occurred. Three dicarboxylic acids (malonic, glutaric and succinic) and levoglucosan were analyzed by liquid chromatography coupled with mass spectrometry (ESI-Q-TOF) and soluble potassium (K+) was analyzed by ion chromatography. The concentration of PM2.5 increased on the days when the highest number of forest fires occurred. A strong correlation was observed between levoglucosan and K+, confirming the hypothesis that both are tracers of biomass burning (r = 0.57, p < 0.05). Levoglucosan (average 367.6 ng m−3, Site 2) was the most abundant compound, followed by succinic acid (average 101.7 ng m−3, Site 2), glutaric acid (average 63.2 ng m−3, Site 2), and malonic acid (average 46.9 ng m−3, Site 2), respectively. The ratio of C3/C4 concentrations ranged from 0.5 to 1.2, with an average of 0.8, which suggests great photochemical activity in the Cuernavaca atmosphere. The ratio of K+/levoglucosan concentrations (0.44) indicates that open fires are the main source of these tracers. The positive correlations between PM2.5 and levoglucosan and succinic and malonic acids suggest that such compounds are contributing to secondary organic aerosol particle formation.