See discussions, stats, and author profiles for this publication at: https://www.researchgate.net/publication/260940191 Chemical composition and sources of particle pollution in affluent and poor neighborhoods of Accra, Ghana Article  in  Environmental Research Letters · December 2013 DOI: 10.1088/1748-9326/8/4/044025 CITATIONS READS 18 155 12 authors, including: Zheng Zhou Kathie Dionisio Baylor College of Medicine United States Environmental Protection Agency 107 PUBLICATIONS   1,237 CITATIONS    33 PUBLICATIONS   812 CITATIONS    SEE PROFILE SEE PROFILE Thiago Gomes Veríssimo Raphael E Arku University of São Paulo University of Massachusetts Amherst 4 PUBLICATIONS   51 CITATIONS    23 PUBLICATIONS   330 CITATIONS    SEE PROFILE SEE PROFILE Some of the authors of this publication are also working on these related projects: CAPAS study View project Life Cycle Analysis-Human Exposure Model View project All content following this page was uploaded by Kathie Dionisio on 09 January 2015. The user has requested enhancement of the downloaded file. Home Search Collections Journals About Contact us My IOPscience Chemical composition and sources of particle pollution in affluent and poor neighborhoods of Accra, Ghana This content has been downloaded from IOPscience. Please scroll down to see the full text. 2013 Environ. Res. Lett. 8 044025 (http://iopscience.iop.org/1748-9326/8/4/044025) View the table of contents for this issue, or go to the journal homepage for more Download details: IP Address: 134.67.237.142 This content was downloaded on 13/03/2014 at 15:08 Please note that terms and conditions apply. IOP PUBLISHING ENVIRONMENTAL RESEARCH LETTERS Environ. Res. Lett. 8 (2013) 044025 (9pp) doi:10.1088/1748-9326/8/4/044025 Chemical composition and sources of particle pollution in affluent and poor neighborhoods of Accra, Ghana Zheng Zhou1,2, Kathie L Dionisio1,2, Thiago G Verissimo3, Americo S Kerr3, Brent Coull2,4, Raphael E Arku2, Petros Koutrakis2, John D Spengler2, Allison F Hughes5, Jose Vallarino2, Samuel Agyei-Mensah6 and Majid Ezzati7 1 Department of Global Health and Population, Harvard School of Public Health, Boston, MA, USA 2 Department of Environmental Health, Harvard School of Public Health, Boston, MA, USA 3 Institute of Physics, University of Sao Paulo, Sao Paulo, Brazil 4 Department of Biostatistics, Harvard School of Public Health, Boston, MA, USA 5 Department of Physics, University of Ghana, Legon, Ghana 6 Department of Geography and Resource Development, University of Ghana, Legon, Ghana 7 Medical Research Council–Public Health England Centre for Environment and Health, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, UK E-mail: majid.ezzati@imperial.ac.uk Received 7 September 2013 Accepted for publication 10 October 2013 Published 30 October 2013 Online at stacks.iop.org/ERL/8/044025 Abstract The highest levels of air pollution in the world now occur in developing country cities, where air pollution sources differ from high-income countries. We analyzed particulate matter (PM) chemical composition and estimated the contributions of various sources to particle pollution in poor and affluent neighborhoods of Accra, Ghana. Elements from earth’s crust were most abundant during the seasonal Harmattan period between late December and late January when Saharan dust is carried to coastal West Africa. During Harmattan, crustal particles accounted for 55 µg m−3 (37%) of fine particle (PM2.5) mass and 128 µg m−3 (42%) of PM10 mass. Outside Harmattan, biomass combustion, which was associated with higher black carbon, potassium, and sulfur, accounted for between 10.6 and 21.3 µg m−3 of fine particle mass in different neighborhoods, with its contribution largest in the poorest neighborhood. Other sources were sea salt, vehicle emissions, tire and brake wear, road dust, and solid waste burning. Reducing air pollution in African cities requires policies related to energy, transportation and urban planning, and forestry and agriculture, with explicit attention to impacts of each strategy in poor communities. Such cross-sectoral integration requires emphasis on urban environment and urban poverty in the post-2015 Development Agenda. Keywords: air pollution, particulate matter, source apportionment, urbanization, sustainable development, Africa S Online supplementary data available from stacks.iop.org/ERL/8/044025/mmedia Content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence. Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI. 1748-9326/13/044025+09$33.00 1 ©c 2013 IOP Publishing Ltd Printed in the UK Environ. Res. Lett. 8 (2013) 044025 Z Zhou et al 1. Introduction the samples were quantified by energy dispersive x-ray fluorescence (ED-XRF) at the Institute of Astronomy, The highest levels of air pollution in the world now occur in Geophysics and Atmospheric Science, University of Sao cities in Asia, Middle East, and Africa [1]. In these settings, Paulo, Brazil. Measured elements in our study included the concentrations of fine particles (less than 2.5 µm in sodium (Na), magnesium (Mg), aluminum (Al), silicon aerodynamic diameter; PM2.5), which are associated with (Si), sulfur (S), chlorine (Cl), potassium (K), calcium (Ca), hazardous effects on health, approach or reach 100 µg m−3, titanium (Ti), vanadium (V), chromium (Cr), nickel (Ni), compared to less than 20 µg m−3 in most European and manganese (Mn), iron (Fe), copper (Cu), zinc (Zn), bromine North American cities [1]. The sources of air pollution in (Br), and lead (Pb). We converted the major crustal elements developing country cities include those that are common to their most abundant oxide forms as most of earth’s crust in high-income nations, e.g., vehicle emissions, as well as consists of mineral oxides. We also converted sulfur (S) to biomass and coal combustion for household and commercial sulfate (SO2−4 ), the most common form in the atmosphere. purposes and resuspended dust from unpaved roads. In coastal Other elements, whose forms in the atmosphere vary by West Africa, sea salt and long-range-transported Saharan dust source, are reported in their elemental form. Gallium (Ga), may also be sources of particles in some seasons [2–4]. selenium (Se), rubidium (Rb), yttrium (Y), niobium (Nb), Yet little is known about the relative contributions of these barium (Ba), and hafnium (Hf) were excluded from the sources to pollution levels in African cities, where the urban analysis because a relatively large number of the measured population is growing faster than any other region; neither is concentrations were below the limit of detection. it known how the source diversity affects particle chemistry, Black carbon (BC) concentrations were estimated which may in turn affect both health hazards and impacts on primarily using data on reflectance coefficients. For 52 anthropogenic climate change. site-days, we also collected co-located PM samples on We conducted a study in Accra, Ghana, one of Africa’s quartz fiber filters, which were used to directly measure fastest growing cities to understand the levels, chemical BC concentrations. We used site-days with both direct properties, and sources of particle pollution. Three quarters measurement and data on reflectance coefficient to develop of sub-Saharan Africa’s population use biomass fuels as a regression equation that related the natural logarithm (ln) of their main source of energy, including over one half of BC concentration to the reflectance coefficient. The regression urban households [5, 6]. In Accra, and other developing equation was then used to estimate the BC concentrations of country cities, there are significant differences in road the remaining samples whose reflectance, but not BC, had conditions, traffic patterns, and fuel use between the affluent been measured. We used the positive matrix factorization neighborhoods and poor ‘slum’ areas [6–8]. For this reason, (PMF) of the elemental mass to identify and quantify the we collected data at sites located in poor and affluent sources of PM at five sites [9]. neighborhoods. Details on methods for particle sample collection, measurement of total and elemental mass concentrations, and 2. Materials and methods the PMF model are described in the supplementary material (available at stacks.iop.org/ERL/8/044025/mmedia). We collected particulate matter (PM) samples between September 2007 and August 2008 in four neighborhoods 3. Results of varying degrees of poverty and affluence. The four neighborhoods lie on a line from the coast to Accra’s northern 3.1. Particle chemical composition boundaries: James Town/Usher Town (JT), Asylum Down (AD), Nima (NM) and East Legon (EL) (figure 1). JT and Particle mass concentrations were reported elsewhere [10]. NM are densely populated low-income communities where Here, we analyzed and report the elemental composition most residents use biomass for cooking at home and for of PM2.5 and PM10; PM10 includes both fine and coarse street food. AD is a middle-class neighborhood and EL is fractions in the respirable range. Total particle mass, crustal an upper-class, sparsely-populated residential neighborhood components like SiO2, and to a lesser extent K peaked where most families live on large plots of land and in modern sharply in all neighborhoods between December and February low-rise homes. Fewer people use biomass fuels in AD and (figure 2), the seasonal Harmattan period when northeast trade EL than in JT and NM. winds blow from the Sahara at an altitude of about 1500 m, Between September 2007 and August 2008, we simulta- carrying large amounts of Saharan dust and emissions from neously operated five monitoring sites in four neighborhoods dry-season bushfires [2–4]. SO2−4 also had a strong seasonal (JT, AD, NM-1, NM-2, and EL). Measurements were done for pattern, peaking in January and August and being lowest one 48-h period every six days. We also used geo-coded data in May and October. The latter months coincide with rainy from the Ghana Population and Housing Census on household seasons, when wet deposition helps remove the water-soluble socioeconomic status and fuel use and data from the Ghana SO2−4 . In contrast to these components, chlorine concentration Survey Department on road locations and types. changed little over time but had a noticeable spatial pattern, PM mass concentrations were measured on a Mettler being highest in JT and lowest in EL; JT also had higher Toledo MT5 microbalance at the Harvard School of sodium (Na) concentrations; see tables 1 and 2. JT is close to Public Health Laboratory. The elemental concentrations of the ocean and hence has more particles from sea spray. Black 2 Environ. Res. Lett. 8 (2013) 044025 Z Zhou et al Figure 1. Study neighborhoods and measurement sites. The polygons on the central panel show census enumeration areas (EAs). Each EA has approximately the same population; hence the area of an EA is inversely related to population density. EAs are categorized according to quintile in terms of per cent of household using biomass fuels. Each color represents a different quintile. The sites were at locations that were typical of each neighborhood’s living environment, with the EL site being far from major traffic and the AD site being next to a road with moderate traffic. In NM we also had a second site next to a road with heavy traffic. The distances of measurement sites to the ocean coast were: JT 0.5 km, AD 3 km, NM 4.5 km, and EL 9 km. carbon, K, and SO2−4 were also higher in JT, the neighborhood in the fine fraction was below 40% for crustal oxides (MgO, with the highest biomass use density (figure 1). K and SO2− Al2O3, SiO2, CaO, TiO2, MnO, and Fe4 2O3) and for elements are linked to biomass burning and BC to emissions from in sea salt (Na and Cl), indicating that they were mostly in the combustion sources including biomass smoke. Potassium in form of coarse particles. In contrast, 60% or more of SO 2− 4 , biomass smoke is emitted mostly as potassium salts such as K, Ni, Zn, Br, Pb and BC mass was in the fine fraction, which can penetrate deeper into lungs. These elements are KCl and K2SO4; with aging, most KCl particles are converted mainly associated with biomass and solid waste burning, to K2SO4 [11, 12]. motor vehicle emissions, and industrial sources. Between 49% and 59% of PM10 mass was in the fine There was strong correlation among the concentrations fraction at different sites (table 3). The proportion of mass of crustal elements (tables S1 and S2, available at 3 Environ. Res. Lett. 8 (2013) 044025 Z Zhou et al Figure 2. Concentrations of total particle mass and of selected elements for (a) PM2.5 and (b) PM10 over the study period at the five measurement sites. Changes along the horizontal direction show variations over time and the spread along the vertical direction shows variation across measurement sites. For comparison, the World Health Organization (WHO) guideline for annual mean PM2.5 concentration is 10 µg m−3. stacks.iop.org/ERL/8/044025/mmedia), especially during non-Harmattan months, when a sea breeze is more frequent. Harmattan (correlation coefficients ≥ 0.9), when the Saharan Similarly, there was moderate correlation among Br, Pb, and dust falls on the city. During Harmattan, crustal elements Zn, which are all present in vehicle emissions, tire and brake were also highly correlated with total particle mass. Sea salt wear, road dust, and in smoke generated from burning solid elements (Na and Cl) were also correlated with one another in waste [13, 14]. 4 Environ. Res. Lett. 8 (2013) 044025 Z Zhou et al Table 1. Average concentrations of total PM2.5 mass and its chemical components at five monitoring sites during the non-Harmattan months. Chemical species AD (n = 35) EL (n = 37) JT (n = 36) NM-1 (n = 39) NM-2 (n = 52) Total massa 27 ± 8 23 ± 8 50 ± 12 28 ± 8 34 ± 9 MgO 103 ± 128 (0.4%)b 141 ± 187 (0.6%) 179 ± 192 (0.4%) 125 ± 155 (0.5%) 132 ± 153 (0.4%) Al2O3 909 ± 936 (3.4%) 1212 ± 1245 (5.4%) 1335 ± 1549 (2.6%) 1103 ± 1140 (4.0%) 1514 ± 1102 (4.4%) SiO2 2334 ± 2603 (8.6%) 3115 ± 3399 (13.8%) 3540 ± 4343 (7.0%) 2814 ± 3165 (10.2%) 3664 ± 2977 (10.7%) CaO 319 ± 223 (1.2%) 351 ± 291 (1.6%) 543 ± 424 (1.1%) 404 ± 264 (1.5%) 635 ± 311 (1.9%) TiO2 53 ± 50 (0.2%) 68 ± 65 (0.3%) 75 ± 83 (0.1%) 64 ± 59 (0.2%) 93 ± 60 (0.3%) MnO 10 ± 6 (<0.1%) 9 ± 7 (<0.1%) 11 ± 9 (<0.1%) 9 ± 7 (<0.1%) 12 ± 6 (<0.1%) Fe2O3 495 ± 372 (1.8%) 604 ± 470 (2.7%) 594 ± 584 (1.2%) 534 ± 420 (1.9%) 771 ± 427 (2.3%) SO2−4 1985 ± 778 (7.3%) 1815 ± 753 (8.1%) 2538 ± 829 (5.0%) 1894 ± 696 (6.8%) 2028 ± 726 (5.9%) Na 295 ± 217 (1.1%) 239 ± 174 (1.1%) 502 ± 336 (1.0%) 284 ± 266 (1.0%) 226 ± 143 (0.7%) K 585 ± 233 (2.2%) 633 ± 230 (2.8%) 1873 ± 414 (3.7%) 858 ± 248 (3.1%) 936 ± 232 (2.7%) Cl 239 ± 269 (0.9%) 152 ± 119 (0.7%) 1450 ± 817 (2.9%) 346 ± 258 (1.2%) 366 ± 209 (1.1%) V 1 ± 1 (<0.1%) 1 ± 1 (<0.1%) 1 ± 1 (<0.1%) 1 ± 1 (<0.1%) 1 ± 1 (<0.1%) Cr 1 ± 1 (<0.1%) 1 ± 1 (<0.1%) 2 ± 1 (<0.1%) 1 ± 1 (<0.1%) 2 ± 1 (<0.1%) Ni 4 ± 1 (<0.1%) 3 ± 1 (<0.1%) 4 ± 1 (<0.1%) 3 ± 2 (<0.1%) 3 ± 1 (<0.1%) Cu 6 ± 5 (<0.1%) 2 ± 2 (<0.1%) 5 ± 4 (<0.1%) 5 ± 4 (<0.1%) 6 ± 6 (<0.1%) Zn 38 ± 15 (0.1%) 15 ± 8 (0.1%) 45 ± 16 (0.1%) 29 ± 13 (0.1%) 32 ± 11 (0.1%) Br 29 ± 22 (0.1%) 10 ± 4 (<0.1%) 36 ± 23 (0.1%) 23 ± 21 (0.1%) 23 ± 19 (0.1%) Sr 2 ± 1 (<0.1%) 3 ± 2 (<0.1%) 4 ± 3 (<0.1%) 3 ± 2 (<0.1%) 4 ± 2 (<0.1%) Zr 1 ± 1 (<0.1%) 2 ± 1 (<0.1%) 2 ± 2 (<0.1%) 1 ± 1 (<0.1%) 2 ± 1 (<0.1%) Pb 14 ± 5 (0.1%) 6 ± 2 (<0.1%) 31 ± 15 (0.1%) 13 ± 4 (<0.1%) 14 ± 4 (<0.1%) BCc 6603 ± 1642 3676 ± 1774 (16.1%) 8613 ± 1509 5176 ± 1584 (18.5%) 6200 ± 1268 (18.2%) (24.4%) (17.2%) % of total mass 52% 52% 43% 49% 49% accounted a Units are in ng m−3 except for total mass, which is in µg m−3. b Mean ± standard deviation. Numbers in parenthesis show the per cent of total mass. c The 52 site-days with direct BC measurements using PM samples on quartz fiber filters also provided data on organic carbon (OC), measured following NIOSH Protocol 5040. For those 52 samples, OC accounted for 11–44% (mean 26%) of total PM mass. Mean OC/BC ratio in these samples was 1.7 (SD 0.6). In these samples, the correlation between OC and BC was around 0.6. 3.2. Source contributions 10.6 µg m−3 in AD and 11.2 µg m−3 in EL. Road dust and traffic aerosols had a more important role in the two sites near We identified 5–6 potential sources for fine particles and traffic routes, one of NM’s sites by a busy road and the AD 4–5 for PM10 at different sites during non-Harmattan months site. A last source, which is likely to be burning of solid waste, (figure 3). The estimated contributions of sea salt to total was identified for fine particles in all neighborhoods except PM2.5 mass ranged between around 2 µg m−3 in NM-2 and affluent EL, being largest in JT where old tires and other solid EL (4.5 and 9 km from the coast) to 13.9 µg m−3 (25% waste are commonly burned. of total PM2.5 mass) in JT (500 m from the coast) during There was about 10 times as much particle mass from non-Harmattan months. Similarly, sea salt contribution to crustal sources during Harmattan as there had been in other PM10 was smallest in EL and largest in JT, accounting for 3 3 months (figure 3). During Harmattan, there was also an6.4 µg m− (14%) and 27.5 µg m− (31%) of total PM10 increase in particle pollution from resuspended road dust and mass, respectively. In contrast to sea salt, crustal sources from biomass burning. The absolute amount of particle mass made up a larger share of total particle mass in EL, the from other sources changed little, leading to a reduction in northernmost neighborhood. For example 38% of PM2.5 and their share of total mass. 46% of PM10 mass in EL were from crustal sources, compared to only 17% and 16% in JT. Despite having a larger share from crustal sources, lower total particle mass in EL meant 4. Strengths and limitations that the absolute contribution of crustal aerosols was only slightly higher than other neighborhoods, e.g., 10.5 µg m−3 To our best knowledge, this paper uses one of the richest data in PM2.5 compared to 9.5 µg m−3 in JT. This higher absolute sets on particle air pollution levels, chemical composition, contribution may have been because more spread-out low- and sources in a developing country city. The unique data rise homes do not block the windblown Saharan or local dust. come from our own measurements in poor and affluent Biomass smoke contributed more particle pollution in neighborhoods and in different seasons, combined with NM and JT, where the density of households who use data from the Population and Housing Census and the biomass fuels is substantially higher [6], than in AD and EL; Survey Department, all with detailed geospatial information. biomass-related particles accounted for 15.7–21.3 µg m−3 of The consistent and comparable data in poor and affluent PM2.5 mass in the former two neighborhoods, compared to neighborhoods alone allow us to examine, for the first time, 5 Environ. Res. Lett. 8 (2013) 044025 Z Zhou et al Table 2. Average concentrations of total PM10 mass and its chemical components at five monitoring sites during the non-Harmattan months. Chemical species AD (n = 33) EL (n = 37) JT (n = 33) NM-1 (n = 40) NM-2 (n = 54) Total massa 55 ± 18 46 ± 19 81 ± 22 51 ± 20 70 ± 21 MgO 454 ± 289 (0.8%)b 446 ± 342 (1%) 741 ± 346 (0.9%) 430 ± 335 (0.8%) 515 ± 329 (0.7%) Al2O3 3026 ± 2220 (5.5%) 3646 ± 2516 (7.9%) 3088 ± 2626 (3.8%) 3239 ± 2535 (6.3%) 4882 ± 2780 (7.0%) SiO2 8484 ± 6441 9749 ± 7245 8764 ± 7635 8744 ± 7126 (17.0%) 12 270 ± 7374 (15.5%) (21.1%) (10.8%) (17.6%) CaO 1520 ± 788 (2.8%) 1340 ± 804 (2.9%) 2260 ± 1023 (2.8%) 1682 ± 958 (3.3%) 2653 ± 1127 (3.8%) TiO2 212 ± 140 (0.4%) 233 ± 151 (0.5%) 215 ± 159 (0.3%) 218 ± 154 (0.4%) 343 ± 182 (0.5%) MnO 26 ± 15 (<0.1%) 24 ± 17 (0.1%) 27 ± 18 (<0.1%) 25 ± 16 (<0.1%) 35 ± 18 (0.1%) Fe2O3 2096 ± 1060 (3.8%) 2171 ± 1110 (4.7%) 1783 ± 1169 (2.2%) 1956 ± 1210 (3.8%) 2895 ± 1261 (4.1%) SO2−4 2601 ± 847 (4.7%) 2138 ± 682 (4.6%) 3301 ± 879 (4.1%) 2276 ± 737 (4.4%) 2625 ± 758 (3.8%) Na 1033 ± 624 (1.9%) 616 ± 463 (1.3%) 2021 ± 838 (2.5%) 739 ± 505 (1.4%) 739 ± 505 (1.4%) K 880 ± 332 (1.6%) 874 ± 328 (1.9%) 2188 ± 490 (2.7%) 1123 ± 354 (2.2%) 1324 ± 356 (1.9%) Cl 2023 ± 930 (3.7%) 1203 ± 570 (2.6%) 4871 ± 1362 (6.0%) 1711 ± 658 (3.3%) 2087 ± 733 (3%) V 3 ± 1 (<0.1%) 3 ± 1 (<0.1%) 2 ± 1 (<0.1%) 2 ± 2 (<0.1%) 3 ± 2 (<0.1%) Cr 4 ± 1 (<0.1%) 4 ± 1 (<0.1%) 4 ± 2 (<0.1%) 3 ± 2 (<0.1%) 5 ± 2 (<0.1%) Ni 3 ± 1 (<0.1%) 3 ± 1 (<0.1%) 3 ± 1 (<0.1%) 3 ± 1 (<0.1%) 3 ± 1 (<0.1%) Cu 10 ± 5 (<0.1%) 4 ± 2 (<0.1%) 8 ± 4 (<0.1%) 8 ± 3 (<0.1%) 11 ± 5 (<0.1%) Zn 55 ± 18 (0.1%) 26 ± 13 (0.1%) 71 ± 27 (0.1%) 41 ± 18 (0.1%) 55 ± 16 (0.1%) Br 35 ± 24 (0.1%) 12 ± 5 (<0.1%) 44 ± 21 (0.1%) 28 ± 23 (0.1%) 32 ± 24 (<0.1%) Sr 8 ± 4 (<0.1%) 8 ± 5 (<0.1%) 14 ± 6 (<0.1%) 10 ± 5 (<0.1%) 13 ± 6 (<0.1%) Zr 5 ± 4 (<0.1%) 6 ± 4 (<0.1%) 5 ± 4 (<0.1%) 5 ± 4 (<0.1%) 8 ± 4 (<0.1%) Pb 22 ± 6 (<0.1%) 9 ± 3 (<0.1%) 36 ± 14 (<0.1%) 17 ± 5 (<0.1%) 21 ± 5 (<0.1%) BC 7407 ± 1664 3617 ± 1450 (7.8%) 9587 ± 1463 5358 ± 1884 (10.5%) 6283 ± 1476 (9.0%) (13.5%) (11.8%) % of total mass 54% 57% 48% 54% 53% accounted a Units are in ng m−3 except for total mass, which is in µg m−3. b Mean ± standard deviation. Numbers in parenthesis show the per cent of total mass. how air pollution levels, composition, and sources differ in for air pollution control in rapidly expanding developing relation to socioeconomic status. country cities like Accra. First, the role of urban biomass Similar to all field measurement studies, our work burning as a source of air pollution creates both policy is affected by some limitations. Logistical difficulties and complexities and opportunities. Large-scale transitions to time-intensive field work restricted our ability to run cleaner fuels such as liquefied petroleum gas (LPG) may multiple measurement sites simultaneously in each study require targeted subsidies for fuel and/or financial assistance neighborhood to assess within-neighborhood variation. It towards the initial cost of an LPG stove for poor households. would have been desirable to conduct consecutive 48 h Perhaps more importantly, sustained use of clean fuels measurements, but this was beyond our resources. requires improving the energy delivery and distribution Limitations in the analysis include the reliance of infrastructure so that people can have regular trouble-free source apportionment analysis on relatively stable source access to fuel purchase, currently not available in poor profiles across samples. In reality, source profiles may neighborhoods [6]. On the other hand, addressing household somewhat differ overtime, even at the same site. The fuel use in cities can take advantage of high population density choice of the number of PM sources is based on the best and urban infrastructure versus in rural areas, where long compromise between the goodness of model fit and the distances and poor roads and energy infrastructures make fuel physical meaningfulness of the resolved factors; we tried the switching more challenging. In addition to urban biomass use, source apportionment with different numbers of factors and long-range transport of particles from wild bushfires or from compared the results before selecting the current number of land clearing/preparation for agriculture by burning may be sources. In addition, labeling PM sources after PMF analysis responsible for urban particle pollution in West Africa [16]. also involves some subjectivity. All of these limitations should Reducing regional biomass pollution requires attention to land inform the design of future research on the sources of urban use and agriculture policies and should be accompanied by air pollution in cities in low- and middle-income countries local strategies for wildfire management [17]. where combustion and non-combustion sources are changing Second, while resuspended dust may seem outside the relatively rapidly. realm of policy interventions, local and regional strategies do exist: road and urban dust can be addressed through 5. Discussion and conclusions paving roads, traffic control, and, where affordable, regular road cleaning. Regional dust pollution is intensified by Our findings on the chemical composition and sources deforestation and desertification, and can be gradually re- of air pollution provide a number of important directions duced through afforestation and grassland restoration [18–21]. 6 Environ. Res. Lett. 8 (2013) 044025 Z Zhou et al Figure 3. Contributions of pollution sources to particle mass during (a) non-Harmattan months, by neighborhood and (b) peak Harmattan (25 December 2007 to 30 January 30 2008). Sea salt is characterized primarily by Na, Cl, and S (in aged sea salt, the Cl ion is replaced by SO2−4 as a result of reaction with sulfuric acid; this chemical transformation is more pronounced in coastal areas than in inland regions [15]). Crustal sources are characterized by Si, Al, Mg, Ti, Mn and Fe. Biomass smoke is primarily characterized by K, Cl, S, and black carbon (BC) [12]. Road dust and traffic particles are characterized by Al, Si, Ca, Fe, and BC. Solid waste burning is characterized by Br [14]. During Harmattan, data from the five sites were pooled to increase sample size, after confirming that source profiles (but not contributions) were similar across sites. Beyond ecological considerations, such strategies should be their health hazards, especially if the harms disproportionately connected with programs related to population growth and affect poor urban communities relative to the benefits. Fourth, mobility, and those that improve the economic conditions of there was a larger contribution from burning of solid waste rural households who rely on land resources. The important in poor neighborhoods, where trash collection is less frequent role of seasonal dust as a pollution source also demonstrates than in affluent neighborhoods. This demonstrates the need the need for research on the acute and chronic health for equitable provision of urban services, now largely absent effects of exposure to crustal particles [22, 23], and whether from poor slums. air pollution regulations in developing countries should be Air pollution regulation and technological advances based on total particle mass or specifically target combustion related to emissions from vehicles, power plants, and sources. factories, have led to cleaner cities in high-income countries. Third, while traffic sources accounted for a relatively Some cities have also benefited from reducing pollution small share of particle pollution in Accra, their absolute from local or regional dust, for example through sweeping contribution towards PM2.5 was over 10 µg m−3 in some and washing roads, stabilizing the road surface with dust neighborhoods, larger than WHO guidelines for total PM2.5 suppressants, and planting trees. Lower particle pollution has concentration. If African cities follow Asian and Middle in turn contributed to improved health [26]. The highest Eastern megacities, where traffic management and pollution pollution levels, and about 90% of the global disease burden is a major policy challenge, there will be even more from air pollution, now occur outside the Americas and traffic-related pollution. Curbing and reducing traffic air Europe [1, 27]. Therefore, while efforts to further reduce air pollution will inevitably require a sustainable pro-poor pollution in these regions continue, there is an urgent need public transportation system, as implemented in cities like to tackle air pollution in cities in the developing world. The Bogota [24]. African countries are a market for old cars diversity of sources demonstrates the need for integration that do not meet emissions standards in Europe and North of policies and interventions across environment, energy, America [25]. 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