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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Public Health</journal-id>
<journal-title>Frontiers in Public Health</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Public Health</abbrev-journal-title>
<issn pub-type="epub">2296-2565</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fpubh.2025.1515009</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Public Health</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Probabilistic human health risk assessment of PM<sub>2.5</sub> exposure in communities affected by local sources and gold mine tailings</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Thabethe</surname> <given-names>Nomsa Duduzile Lina</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
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<role content-type="https://credit.niso.org/contributor-roles/formal-analysis/"/>
<role content-type="https://credit.niso.org/contributor-roles/methodology/"/>
<role content-type="https://credit.niso.org/contributor-roles/software/"/>
<role content-type="https://credit.niso.org/contributor-roles/validation/"/>
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</contrib>
<contrib contrib-type="author">
<name><surname>Makonese</surname> <given-names>Tafadzwa</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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</contrib>
<contrib contrib-type="author">
<name><surname>Masekameni</surname> <given-names>Daniel</given-names></name>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
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</contrib>
<contrib contrib-type="author">
<name><surname>Brouwer</surname> <given-names>Derk</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
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<aff id="aff1"><sup>1</sup><institution>Department of Environmental Sciences, University of South Africa</institution>, <addr-line>Florida</addr-line>, <country>South Africa</country></aff>
<aff id="aff2"><sup>2</sup><institution>Health Sciences Faculty, School of Public Health, University of the Witwatersrand</institution>, <addr-line>Johannesburg</addr-line>, <country>South Africa</country></aff>
<aff id="aff3"><sup>3</sup><institution>Department of Development Studies, University of South Africa</institution>, <addr-line>Pretoria</addr-line>, <country>South Africa</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: Mohsen Saeedi, University Canada West, Canada</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: Mohamed F. Yassin, Kuwait Institute for Scientific Research, Kuwait</p>
<p>Adagunodo Theophilus Aanuoluwa, Covenant University, Nigeria</p>
<p>Aydin Shishegaran, Bauhaus-Universit&#x00E4;t Weimar, Germany</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Nomsa Duduzile Lina Thabethe, <email>ethabend@unisa.ac.za</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>28</day>
<month>07</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>13</volume>
<elocation-id>1515009</elocation-id>
<history>
<date date-type="received">
<day>22</day>
<month>10</month>
<year>2024</year>
</date>
<date date-type="accepted">
<day>15</day>
<month>07</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Thabethe, Makonese, Masekameni and Brouwer.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Thabethe, Makonese, Masekameni and Brouwer</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<p>Epidemiological studies have found that exposure to fine particulate matter (PM<sub>2.5</sub>) poses potential human health risks, including respiratory, cardiovascular and cerebrovascular diseases. This study aimed to assess the potential human health risks associated with exposure to PM<sub>2.5</sub> in the eMbalenhle community which is near gold mine Tailings Storage Facilities (TSFs). Ambient PM<sub>2.5</sub> concentrations were measured for 1&#x202F;year (from February 2022 to February 2023) using the Clarity Node-S low-cost monitor (LCM). The United States Environmental Protection Agency (USEPA) equations were used to estimate the carcinogenic and non-carcinogenic health risks associated with exposure to PM<sub>2.5</sub> in toddlers, children, adults and the older adult. Lastly, a probabilistic Human Health Risk Assessment (HHRA) model, which employs Monte Carlo simulations (MCS), was applied to assess the sensitivity and uncertainty risks. The annual PM<sub>2.5</sub> Geometric Mean (GM) concentration were 17, with a Standard Deviation of (SD) of 10.4 and a Geometric Standard Deviation (GSD) of 1.69&#x202F;&#x03BC;g/m<sup>3</sup>. This was below the South African annual National Ambient Air Quality Standards (NAAQS) of 20&#x202F;&#x03BC;g/m<sup>3</sup>. However, this concentration exceeded the World Health Organization (WHO) guidelines and the USEPA annual limit values of 5 and 9&#x202F;&#x03BC;g/m<sup>3</sup>, respectively. For the WHO guidelines, South African and USEPA NAAQS, the HQ was highest at the 95th percentile for all subgroups. For the South African NAAQS, the HQ was estimated to be 0.9 for all subgroups, indicating safe levels. When utilizing the USEPA NAAQS, a value of 2.5 was reported, while the WHO guidelines recorded the highest HQ of 3.5, indicating unsafe levels. This demonstrated that the SA NAAQS underestimated exposure to PM<sub>2.5</sub> concentrations. Probabilistic HHRA assessed potential cancer risk (CR) due to continuous exposure to PM<sub>2.5</sub> concentrations. For both male and female elders, the CR was approximately 1 in 10, meaning that about 100,000 out of 1,000,000 exposed elders were at an increased risk of developing cancer over their lifetime. The study recommends revising the current South African PM<sub>2.5</sub> NAAQS to adopt more stringent measures and align them to international benchmarks to safeguard the public from adverse health effects due to PM<sub>2.5</sub> exposure.</p>
</abstract>
<kwd-group>
<kwd>fine particulate matter</kwd>
<kwd>exposure assessment</kwd>
<kwd>Monte Carlo simulations</kwd>
<kwd>sensitivity analysis</kwd>
<kwd>mining activities</kwd>
</kwd-group>
<counts>
<fig-count count="4"/>
<table-count count="5"/>
<equation-count count="3"/>
<ref-count count="84"/>
<page-count count="12"/>
<word-count count="8434"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Environmental Health and Exposome</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1">
<label>1</label>
<title>Introduction</title>
<p>Ambient air pollution is regarded as a significant threat to human health. According to the World Health Organization (<xref ref-type="bibr" rid="ref1">1</xref>), the combined effects of ambient air pollution and household air pollution account for 6.7 million premature deaths globally. Fine particulate matter, with an aerodynamic diameter of 2.5&#x202F;&#x03BC;m (PM<sub>2.5</sub>), has been associated with many adverse health outcomes (<xref ref-type="bibr" rid="ref2 ref3 ref4 ref5">2&#x2013;5</xref>) because it can penetrate deeper into the alveolar regions of the lungs (<xref ref-type="bibr" rid="ref6">6</xref>, <xref ref-type="bibr" rid="ref7">7</xref>). Human health risks of exposure to PM<sub>2.5</sub> extend beyond respiratory diseases to include cerebrovascular and cardiovascular diseases (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref9">9</xref>), lung cancer, cardiopulmonary mortality, stroke, asthma, arrhythmia (<xref ref-type="bibr" rid="ref10">10</xref>, <xref ref-type="bibr" rid="ref11">11</xref>). Exposure to PM<sub>2.5</sub> affects individuals differently based on their health status, age (<xref ref-type="bibr" rid="ref12">12</xref>), gender and duration of exposure (<xref ref-type="bibr" rid="ref13">13</xref>).</p>
<p>Vulnerable population sub-groups are likely to develop diseases due to lifetime PM<sub>2.5</sub> exposure to PM<sub>2.5</sub> (<xref ref-type="bibr" rid="ref14">14</xref>). These groups include pregnant women, infants and children. Children breathe faster than adults because smaller lungs require more frequent breaths to meet oxygen demands (<xref ref-type="bibr" rid="ref15">15</xref>, <xref ref-type="bibr" rid="ref16">16</xref>). Exposure to high PM<sub>2.5</sub> in these groups can affect how their lungs develop over time, increasing their chances of developing lung diseases (<xref ref-type="bibr" rid="ref17">17</xref>). Exposure to PM<sub>2.5</sub> during pregnancy can impact fetal development and may have long-term health consequences (<xref ref-type="bibr" rid="ref18">18</xref>, <xref ref-type="bibr" rid="ref19">19</xref>). The physiological development, high Inhalation Rate (IR), Body Weight (BW), Exposure Duration (ED) and Exposure Frequency (EF) are some factors that make individuals vulnerable to the adverse health risks of PM<sub>2.5</sub> exposure (<xref ref-type="bibr" rid="ref20">20</xref>). Organs such as the lungs and heart undergo significant maturation over time (<xref ref-type="bibr" rid="ref21">21</xref>). Exposure to PM<sub>2.5</sub> during these stages of organ development can lead to long-term health risks (<xref ref-type="bibr" rid="ref22">22</xref>). The older adult are more at risk of developing adverse health risks due to weakened respiratory and cardiovascular systems (<xref ref-type="bibr" rid="ref23">23</xref>). Furthermore, pre-existing medical conditions, including asthma, heart disease and chronic obstructive pulmonary disease (<xref ref-type="bibr" rid="ref24">24</xref>), increase their vulnerability to the harmful effects of pollution (<xref ref-type="bibr" rid="ref25">25</xref>).</p>
<p>Fine particulate matter (PM<sub>2.5</sub>) is emitted from natural and anthropogenic sources (<xref ref-type="bibr" rid="ref26">26</xref>). Natural sources of PM<sub>2.5</sub> include forest fires and volcanic eruptions. Forest fires emit huge amounts of PM<sub>2.5</sub> from the combustion of vegetation and biomass (<xref ref-type="bibr" rid="ref27">27</xref>). Volcanic eruptions release ash and PM<sub>2.5</sub> into the atmosphere. Anthropogenic sources of PM<sub>2.5</sub> include industrial processes, domestic fuel burning, mining operations and agricultural activities. Burning of wood, coal and other solid fuels for residential heating and cooking also emits PM<sub>2.5</sub> (<xref ref-type="bibr" rid="ref28">28</xref>). Gold mine tailings storage facilities (TSFs) are also a potential source of PM<sub>2.5</sub> emissions. The TSFs are designed to store waste generated during mineral extraction and processing. These tailings consist of crushed rocks, particles and residuals of chemicals left over from the gold extraction process (<xref ref-type="bibr" rid="ref29">29</xref>).</p>
<p>PM<sub>2.5</sub> comprises a complex mixture of biological and chemical components (<xref ref-type="bibr" rid="ref30">30</xref>). The chemical and biological components of PM<sub>2.5</sub> may originate from various sources (<xref ref-type="bibr" rid="ref31">31</xref>). The biological components of PM<sub>2.5</sub> include bacteria, fungi, viruses and pollen (<xref ref-type="bibr" rid="ref32">32</xref>). The chemical components of PM<sub>2.5</sub> include organic compounds (<xref ref-type="bibr" rid="ref33">33</xref>), inorganic compounds (<xref ref-type="bibr" rid="ref34">34</xref>) and trace elements (<xref ref-type="bibr" rid="ref35">35</xref>). The physicochemical properties of fine particulate matter influence their toxicity and health impacts. Particles with larger surface areas and reactive chemical elements, can induce oxidative stress and inflammation, resulting in adverse respiratory and cardiovascular outcomes (<xref ref-type="bibr" rid="ref36">36</xref>).</p>
<p>The assessment of exposure to PM<sub>2.5</sub> is a complex process. It requires information about the sources, site selection and data quality assurance (<xref ref-type="bibr" rid="ref37">37</xref>). PM<sub>2.5</sub> concentrations vary spatially due to differences in emission sources, meteorological conditions, and topographical features. Furthermore, PM<sub>2.5</sub> concentrations can fluctuate over time due to diurnal patterns and seasonal variations (<xref ref-type="bibr" rid="ref38">38</xref>). Human health risks can be assessed by applying the HHRA model (<xref ref-type="bibr" rid="ref39">39</xref>), which estimates the likelihood of adverse human health risks associated with PM<sub>2.5</sub> exposure (<xref ref-type="bibr" rid="ref40">40</xref>). Most studies have used deterministic HHRA models to assess potential human health risks (<xref ref-type="bibr" rid="ref41 ref42 ref43">41&#x2013;43</xref>). A deterministic HHRA model uses single-point estimates for input parameters to calculate specific risk values. One of the advantages of deterministic risk assessment is its simplicity. The disadvantage is its inability to account for the variability among individuals and the uncertainties in environmental data (<xref ref-type="bibr" rid="ref44">44</xref>).</p>
<p>This study used a probabilistic HHRA model to estimate the potential human health risks of continuous exposure to PM<sub>2.5</sub> concentrations. The probabilistic HHRA model was chosen because it uses statistical techniques to account for variability and uncertainty in risk estimates (<xref ref-type="bibr" rid="ref45">45</xref>). Furthermore, the model employs Monte Carlo simulations to generate a distribution of risk estimates based on random sampling from the probability distributions of input parameters (<xref ref-type="bibr" rid="ref46">46</xref>). The advantage of probabilistic HHRA provides a more complete picture of potential health risks by estimating the range and likelihood of different outcomes. The disadvantage is that it requires detailed data on the distribution of input parameters (<xref ref-type="bibr" rid="ref47">47</xref>).</p>
<p>This study introduces a novel approach by applying a probabilistic Human Health Risk Assessment (HHRA) to evaluate the health risks associated with PM<sub>2.5</sub> exposure in eMbalenhle, a community near gold mine tailings storage facilities (TSFs). While most existing studies rely on deterministic risk assessments that often fail to capture the inherent uncertainties and variability in PM<sub>2.5</sub> exposure (<xref ref-type="bibr" rid="ref39">39</xref>, <xref ref-type="bibr" rid="ref41">41</xref>, <xref ref-type="bibr" rid="ref43">43</xref>), this study addresses these limitations by adopting a probabilistic framework. Furthermore, the application of this method to communities affected by gold mine TSFs remains limited in the current literature. Importantly, this is the first study to assess human health risks in eMbalenhle using PM<sub>2.5</sub> data collected from low-cost monitors (LCMs), offering a cost-effective and practical strategy for air quality and risk assessment in resource-constrained settings. The findings of this study will contribute to Sustainable Development Goal 3 (SDG 3). SDG 3 aims at ensuring good health and well-being for all. Monitoring the ambient PM<sub>2.5</sub> contributes to achieving Target 3.9 of SDG 3, which addresses environmental pollution and its health consequences (<xref ref-type="bibr" rid="ref48">48</xref>).</p>
</sec>
<sec sec-type="materials|methods" id="sec2">
<label>2</label>
<title>Methods and materials</title>
<sec id="sec3">
<label>2.1</label>
<title>Study design</title>
<p>The study followed a cross-sectional design following quantitative data collection and analysis methods.</p>
</sec>
<sec id="sec4">
<label>2.2</label>
<title>Study area</title>
<p>eMbalenhle (&#x2212;26&#x00B0;550613&#x00B0;S; 29.078937&#x00B0;E) is in the Govan Mbeki Municipality, Mpumalanga, South Africa. eMbalenhle has a population of 118,889 people with an annual growth of 2.5% (<xref ref-type="bibr" rid="ref49">49</xref>). eMbalenhle is known for its gold and coal mining operations, which are potential sources of PM<sub>2.5</sub>. The area falls within the Highveld Priority Area (HPA). This area was declared an air pollution &#x201C;hotspot&#x201D; in terms of Section 18 (<xref ref-type="bibr" rid="ref5">5</xref>) of the National Ambient Air Quality Act, Act 39 of 2004 (<xref ref-type="bibr" rid="ref50">50</xref>). The town is close to industries, open-cast mines, and coal-fired power stations. As of the 16th of July 2024, the real-time Air Quality Index (AQI) displayed a PM<sub>2.5</sub> concentration in eMbalenhle of 155&#x202F;&#x03BC;g/m<sup>3</sup>, about 31 times above the WHO annual air quality Guideline value (<xref ref-type="bibr" rid="ref51">51</xref>). This further indicated an unhealthy situation for vulnerable groups living in the area (<xref ref-type="bibr" rid="ref52">52</xref>).</p>
</sec>
<sec id="sec5">
<label>2.3</label>
<title>Data collection and analysis</title>
<p>The PM<sub>2.5</sub> emissions were measured at the Sasol Recreation Centre (&#x2212;26&#x00B0;550613&#x00B0;S; 29.078937&#x00B0;E) in eMbalenhle for 1&#x202F;year (February 2022 to February 2023) using Clarity Node-S low-cost monitors (LCM) (<xref ref-type="bibr" rid="ref53">53</xref>). These LCM measured PM<sub>2.5</sub> concentrations every 15&#x202F;min in micrograms per cubic meter (&#x03BC;g/m<sup>3</sup>). The ambient PM<sub>2.5</sub> data monitored by the government ambient air monitoring station (also collocated at the Sasol Community Recreation Centre) for the same period was used as reference data. The reference data was used to compare and validate the data collected with the LCM. Both data sets (LCM and reference data) underwent quality control to ensure that the monitored and reference data were not erroneous (<xref ref-type="bibr" rid="ref54">54</xref>). The meteorological data for the same period (February 2022 to February 2023) was obtained from the South African Air Quality Information System website (<xref ref-type="bibr" rid="ref55">55</xref>). The average annual PM<sub>2.5</sub> concentrations were calculated in a Microsoft Excel sheet and compared with the SA NAAQS, USEPA NAAQS and the WHO Guidelines. The PM<sub>2.5</sub> annual Reference Concentrations (Rfc) values used in this study are given in <xref ref-type="table" rid="tab1">Table 1</xref>.</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Local and international ambient PM<sub>2.5</sub> annual reference concentration values.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top" rowspan="2">Standard</th>
<th align="center" valign="top">Reference value</th>
<th align="left" valign="top" rowspan="2">Description</th>
</tr>
<tr>
<th align="center" valign="top">(&#x03BC;g/m<sup>3</sup>)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">NAAQS (SA)</td>
<td align="center" valign="middle">20</td>
<td align="left" valign="middle">National Standard</td>
</tr>
<tr>
<td align="left" valign="middle">US EPA (USA)</td>
<td align="center" valign="middle">9</td>
<td align="left" valign="middle">National Standard</td>
</tr>
<tr>
<td align="left" valign="middle">WHO</td>
<td align="center" valign="middle">5</td>
<td align="left" valign="middle">Guidelines</td>
</tr>
</tbody>
</table>
</table-wrap>
</sec>
<sec id="sec6">
<label>2.4</label>
<title>Probabilistic human health risk assessment</title>
<p>The population of eMbalenhle was divided into eight sub-groups because of the differences in exposure duration and development stages. The eight sub-groups included male and female toddlers (1&#x2013;2&#x202F;years) because their bodies are still developing and they have low IR; male and female children (6&#x2013;11&#x202F;years) because their bodies have developed and they have increased IR; male and female adults (21&#x2013;60&#x202F;years) because their bodies are fully developed and they have a much higher IR as compared to the toddlers and children; and male and female elders (61&#x2013;70&#x202F;years) because their health is weakening (<xref ref-type="bibr" rid="ref56">56</xref>).</p>
<sec id="sec7">
<label>2.4.1</label>
<title>Monte Carlo simulation</title>
<p>Monte Carlo Simulation (MCS) was employed to generate samples from probability distributions, using an Oracle Crystal Ball spreadsheet-based application for predictive modeling. parameters, including PM<sub>2.5</sub> concentrations (C<sub>air</sub>), EF, Exposure Time (ET), ED, and Average Time (AT), were considered as variables in the model. The ET, EF, ED and AT parameters were allocated triangular, uniform and normal distributions. The C<sub>air</sub> was allocated a lognormal distribution. The model used Geometric Mean (GM) and Geometric Standard Deviation (GSD) of the annual PM<sub>2.5</sub> concentrations as C<sub>air</sub>.</p>
<p><xref ref-type="table" rid="tab2">Table 2</xref> lists all the variables used in the probabilistic HHRA model. The annual GM and GSD PM<sub>2.5</sub> concentrations used in the model were measured from February 2022 to February 2023. The ET was assumed to be 16 (minimum), 18 (mode), and 20 (maximum) hours for toddlers and children (<xref ref-type="bibr" rid="ref16">16</xref>, <xref ref-type="bibr" rid="ref22">22</xref>, <xref ref-type="bibr" rid="ref24">24</xref>), and 20, 22, 24 for adults and elders. The EF was estimated based on the assumption that all population sub-groups leave the area for a maximum of 1&#x202F;month, which translates to 335&#x202F;days per year and a minimum of 2&#x202F;weeks for vacation (i.e., the minimum EF is 350&#x202F;days per year). The worst-case scenario assumed that all population subgroups are exposed 365&#x202F;days per year. The AT for CR was based on chronic exposure during the lifetime. Lifetime values were obtained from the life-expectancy data according to the national census and population estimates (<xref ref-type="bibr" rid="ref57">57</xref>). Population estimates for life expectancy from 2002 to 2022 were used to compute the life expectancy arithmetic mean and the standard deviation values used in our model.</p>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Variables used in the probabilistic human health risk assessment model.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Parameter</th>
<th align="left" valign="top">Unit</th>
<th align="left" valign="top">Distribution</th>
<th align="left" valign="top">Value</th>
<th align="left" valign="top">Source</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle">C<sub>air</sub></td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Lognormal</td>
<td align="left" valign="middle">GM 17 (GSD 1.69)</td>
<td align="left" valign="middle">PM<sub>2.5</sub> Annual Average Concentrations (<xref ref-type="bibr" rid="ref53">53</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">ET (Toddler)</td>
<td align="left" valign="middle">hours/day</td>
<td align="left" valign="middle">Triangle</td>
<td align="left" valign="middle">Min-mode-max 18&#x2013;22&#x2013;24</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">ET (Child)</td>
<td align="left" valign="middle">hours/day</td>
<td align="left" valign="middle">Triangle</td>
<td align="left" valign="middle">16&#x2013;22&#x2013;24</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">ET (Adult)</td>
<td align="left" valign="middle">hours/day</td>
<td align="left" valign="middle">Triangle</td>
<td align="left" valign="middle">20&#x2013;22&#x2013;24</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">ET (Elder)</td>
<td align="left" valign="middle">hours/day</td>
<td align="left" valign="middle">Triangle</td>
<td align="left" valign="middle">20&#x2013;22&#x2013;24</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">AT (CR) &#x2013; All Males</td>
<td align="left" valign="middle">years</td>
<td align="left" valign="middle">Normal</td>
<td align="left" valign="middle">57.26&#x202F;&#x00B1;&#x202F;4.71</td>
<td align="left" valign="middle">(<xref ref-type="bibr" rid="ref49">49</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">AT (CR) &#x2013; All Females</td>
<td align="left" valign="middle">years</td>
<td align="left" valign="middle">Normal</td>
<td align="left" valign="middle">62.19&#x202F;&#x00B1;&#x202F;5.53</td>
<td align="left" valign="middle">(<xref ref-type="bibr" rid="ref49">49</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">ED (Toddler)</td>
<td align="left" valign="middle">years</td>
<td align="left" valign="middle">Uniform</td>
<td align="left" valign="middle">Min-max 1&#x2013;2</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">ED (Child)</td>
<td align="left" valign="middle">years</td>
<td align="left" valign="middle">Uniform</td>
<td align="left" valign="middle">6&#x2013;11</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">ED (Adult)</td>
<td align="left" valign="middle">years</td>
<td align="left" valign="middle">Uniform</td>
<td align="left" valign="middle">21&#x2013;60</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">ED (older adult)</td>
<td align="left" valign="middle">years</td>
<td align="left" valign="middle">Uniform</td>
<td align="left" valign="middle">61&#x2013;70</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">EF</td>
<td align="left" valign="middle">days/year</td>
<td align="left" valign="middle">Triangle</td>
<td align="left" valign="middle">335&#x2013;350&#x2013;365</td>
<td align="left" valign="middle">(Section 2.3.1)</td>
</tr>
<tr>
<td align="left" valign="middle">Rfc (Annual PM<sub>2.5</sub> -SA NAAQS)</td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">20</td>
<td align="left" valign="middle">(<xref ref-type="bibr" rid="ref50">50</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Rfc (Annual PM<sub>2.5</sub> &#x2013; WHO Guidelines)</td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">5</td>
<td align="left" valign="middle">(<xref ref-type="bibr" rid="ref51">51</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">Rfc (Annual PM<sub>2.5</sub> US EPA NAAQS)</td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">9</td>
<td align="left" valign="middle">(<xref ref-type="bibr" rid="ref53">53</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">IUR</td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">0.008</td>
<td align="left" valign="middle">(<xref ref-type="bibr" rid="ref63">63</xref>)</td>
</tr>
<tr>
<td align="left" valign="middle">C<sub>air-adj (HQ)</sub></td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">Calculated</td>
<td align="left" valign="middle">Output</td>
</tr>
<tr>
<td align="left" valign="middle">C<sub>air-adj (CR)</sub></td>
<td align="left" valign="middle">&#x03BC;g/m<sup>3</sup></td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">Calculated</td>
<td align="left" valign="middle">Output</td>
</tr>
<tr>
<td align="left" valign="middle">HQ (SA-NAAQS)</td>
<td align="left" valign="middle">Unitless</td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">Calculated</td>
<td align="left" valign="middle">Output</td>
</tr>
<tr>
<td align="left" valign="middle">HQ (WHO Guidelines)</td>
<td align="left" valign="middle">Unitless</td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">Calculated</td>
<td align="left" valign="middle">Output</td>
</tr>
<tr>
<td align="left" valign="middle">HQ (US EPA NAAQS)</td>
<td align="left" valign="middle">Unitless</td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">Calculated</td>
<td align="left" valign="middle">Output</td>
</tr>
<tr>
<td align="left" valign="middle">Cancer Risk</td>
<td align="left" valign="middle">Unitless</td>
<td align="left" valign="middle">Not Applicable</td>
<td align="left" valign="middle">Calculated</td>
<td align="left" valign="middle">Output</td>
</tr>
</tbody>
</table>
</table-wrap>
<p>Once the distributions of the variables were determined as normal, lognormal or triangle, the model randomly selected a value for each variable and calculated the risk. In MCS, each calculation is called an iteration, and a set of iterations is called a simulation (<xref ref-type="bibr" rid="ref58">58</xref>). The probabilistic health risk distribution was obtained by running 10,000 iterations (<xref ref-type="bibr" rid="ref59">59</xref>, <xref ref-type="bibr" rid="ref60">60</xref>).</p>
<p>The HQ was calculated using <xref ref-type="disp-formula" rid="EQ1">Equation 1</xref> for each population sub-group to assess the non-carcinogenic health risks associated with exposure to PM<sub>2.5</sub>.<disp-formula id="EQ1">
<label>(1)</label>
<mml:math id="M1">
<mml:mi>HQ</mml:mi>
<mml:mo>=</mml:mo>
<mml:msub>
<mml:mi mathvariant="normal">C</mml:mi>
<mml:mrow>
<mml:mi>air</mml:mi>
<mml:mo>&#x2212;</mml:mo>
<mml:mi>adj</mml:mi>
</mml:mrow>
</mml:msub>
<mml:mo>/</mml:mo>
<mml:mi>Rfc</mml:mi>
</mml:math>
</disp-formula></p>
<p>Where:</p>
<p>HQ is unitless, representing the ratio of the concentration of PM<sub>2.5</sub> in the air (C<sub>air</sub>) to the Reference Concentration (Rfc), (<xref ref-type="bibr" rid="ref61">61</xref>). Since the Rfc assumes continuous exposure 24&#x202F;h/7&#x202F;days a week and 52&#x202F;weeks/year, the measured concentration of PM<sub>2.5</sub> must be adjusted to the actual duration of the exposure. The adjusted PM<sub>2.5</sub> concentrations (C<sub>air-adj</sub>) were estimated using <xref ref-type="disp-formula" rid="EQ2">Equation 2</xref> derived from the USEPA (<xref ref-type="bibr" rid="ref61">61</xref>).<disp-formula id="EQ2">
<label>(2)</label>
<mml:math id="M2">
<mml:msub>
<mml:mi mathvariant="normal">C</mml:mi>
<mml:mrow>
<mml:mi>air</mml:mi>
<mml:mo>&#x2212;</mml:mo>
<mml:mi>adj</mml:mi>
</mml:mrow>
</mml:msub>
<mml:mo>=</mml:mo>
<mml:msub>
<mml:mi mathvariant="normal">C</mml:mi>
<mml:mi>air</mml:mi>
</mml:msub>
<mml:mo>&#x00D7;</mml:mo>
<mml:mo stretchy="true">(</mml:mo>
<mml:mi>ET</mml:mi>
<mml:mo>&#x00D7;</mml:mo>
<mml:mn>1</mml:mn>
<mml:mo>/</mml:mo>
<mml:mn>24</mml:mn>
<mml:mspace width="0.25em"/>
<mml:mtext>hours</mml:mtext>
<mml:mo stretchy="true">)</mml:mo>
<mml:mo>&#x00D7;</mml:mo>
<mml:mo stretchy="true">(</mml:mo>
<mml:mi>EF</mml:mi>
<mml:mo>&#x00D7;</mml:mo>
<mml:mn>1</mml:mn>
<mml:mo>/</mml:mo>
<mml:mn>365</mml:mn>
<mml:mo stretchy="true">)</mml:mo>
<mml:mo>&#x00D7;</mml:mo>
<mml:mi>ED</mml:mi>
<mml:mo>/</mml:mo>
<mml:mi>AT</mml:mi>
</mml:math>
</disp-formula></p>
<p>Where:<list list-type="bullet">
<list-item>
<p>C<sub>air</sub> =&#x202F;Concentration of contaminant in air (&#x03BC;g/m<sup>3</sup>)</p>
</list-item>
<list-item>
<p>ET&#x202F;=&#x202F;Exposure time (hours/day)</p>
</list-item>
<list-item>
<p>EF&#x202F;=&#x202F;Exposure frequency (days/year)</p>
</list-item>
<list-item>
<p>ED&#x202F;=&#x202F;Exposure duration (years)</p>
</list-item>
<list-item>
<p>AT&#x202F;=&#x202F;Averaging time (years)</p>
</list-item>
</list></p>
<p>For non-carcinogenic health risks/sub-chronic exposure, or when evaluating acute exposures or short-term events where the exposure duration aligns with the exposure averaging time, AT equals ED; therefore, AT and ED can be left out of <xref ref-type="disp-formula" rid="EQ2">Equation 2</xref>. In contrast, for carcinogenic risk/chronic exposure, the AT is equal to the estimated life expectancy.</p>
<p>The Rfc(s) represent the PM<sub>2.5</sub> concentration values unlikely to cause adverse human health risks over a specified period. The Rfc(s) were derived from toxicological studies and are expressed in the same units as C<sub>air</sub> (i.e., &#x03BC;g/m<sup>3</sup>). According to USEPA (<xref ref-type="bibr" rid="ref62">62</xref>), if the HQ is less or equal to one (HQ&#x202F;&#x2264;&#x202F;1), the concentration of PM<sub>2.5</sub> (C<sub>air</sub>) is equal to or less than the Rfc. If the HQ is greater than one (HQ&#x202F;&#x003E;&#x202F;1), there is an increased likelihood of developing non-carcinogenic adverse health outcomes.</p>
<p>The CR was calculated using <xref ref-type="disp-formula" rid="EQ3">Equation 3</xref> for each population sub-group to assess the carcinogenic health risks associated with exposure to PM<sub>2.5</sub>.<disp-formula id="EQ3">
<label>(3)</label>
<mml:math id="M3">
<mml:mi>CR</mml:mi>
<mml:mo>=</mml:mo>
<mml:mi>IUR</mml:mi>
<mml:mo>&#x00D7;</mml:mo>
<mml:msub>
<mml:mi mathvariant="normal">C</mml:mi>
<mml:mrow>
<mml:mi>air</mml:mi>
<mml:mo>&#x2212;</mml:mo>
<mml:mi>adj</mml:mi>
</mml:mrow>
</mml:msub>
</mml:math>
</disp-formula></p>
<p>Where:</p>
<p>CR is the cancer risk, which represents the estimated probability of developing cancer over a lifetime due to exposure to PM<sub>2.5</sub> through inhalation.</p>
<p>IUR is the inhalation unit risk, representing the increased risk of cancer per unit exposure to PM<sub>2.5</sub> through inhalation. The IUR for PM<sub>2.5</sub> is 0.008&#x202F;&#x03BC;g/m<sup>3</sup> (<xref ref-type="bibr" rid="ref63">63</xref>).</p>
<p>A value greater than 1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;04</sup> (1 in 10,000) indicates a significant CR and may indicate a need for regulatory action or intervention to reduce exposure, as it exceeds the accepted risk threshold. On the other hand, a value less than 1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;06</sup> (1 in 1,000,000) indicates a negligible or &#x201C;acceptable&#x201D; risk. It can be ignored as it does not require regulatory action or interventions to reduce exposure (<xref ref-type="bibr" rid="ref64">64</xref>).</p>
</sec>
</sec>
</sec>
<sec id="sec8">
<label>3</label>
<title>Ethical considerations</title>
<p>The study was approved by the University of the Witwatersrand Human Research Ethics Committee [HREC] (No: HRECNMW21/05/09).</p>
</sec>
<sec sec-type="results" id="sec9">
<label>4</label>
<title>Results</title>
<sec id="sec10">
<label>4.1</label>
<title>Probabilistic human health risk assessment</title>
<sec id="sec11">
<label>4.1.1</label>
<title>Adjusted PM<sub>2.5</sub> concentrations for non-carcinogenic and carcinogenic health risks</title>
<p>The adjusted PM<sub>2.5</sub> concentrations for non and carcinogenic health risks of the different population sub-groups in eMbalenhle are presented in <xref ref-type="table" rid="tab3">Table 3</xref>. The 50th, 75th, and 95th percentile for adjusted PM<sub>2.5</sub> concentrations for non-cancer risks was slightly higher in male and female adults compared to other subgroups due to the higher estimated ET. The 50<sup>th</sup> percentile (median) adjusted PM<sub>2.5</sub> concentrations for CR ranged from 0.4&#x202F;&#x03BC;g/m<sup>3</sup> (male and female toddlers and children) and 10.9&#x202F;&#x03BC;g/m<sup>3</sup> (male elders) due to the different estimates of the AT.</p>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>The adjusted PM<sub>2.5</sub> concentrations (&#x03BC;g/m<sup>3</sup>) for non and carcinogenic health risks.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top" rowspan="2">Sub-groups</th>
<th align="center" valign="top" colspan="2">50th percentile</th>
<th align="center" valign="top" colspan="2">75th percentile</th>
<th align="center" valign="top" colspan="2">95th percentile</th>
</tr>
<tr>
<th align="center" valign="top">&#x002A;NCR</th>
<th align="center" valign="top">&#x002A;&#x002A;CR</th>
<th align="center" valign="top">&#x002A;NCR</th>
<th align="center" valign="top">&#x002A;&#x002A;CR</th>
<th align="center" valign="top">&#x002A;NCR</th>
<th align="center" valign="top">&#x002A;&#x002A;CR</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Male toddlers</td>
<td align="center" valign="top">14.4</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">15.6</td>
<td align="center" valign="top">0.5</td>
<td align="center" valign="top">17.4</td>
<td align="center" valign="top">0.6</td>
</tr>
<tr>
<td align="left" valign="top">Female toddlers</td>
<td align="center" valign="top">14.5</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">15.6</td>
<td align="center" valign="top">0.4</td>
<td align="center" valign="top">17.4</td>
<td align="center" valign="top">0.5</td>
</tr>
<tr>
<td align="left" valign="top">Male children</td>
<td align="center" valign="top">14.0</td>
<td align="center" valign="top">2.2</td>
<td align="center" valign="top">15.3</td>
<td align="center" valign="top">2.6</td>
<td align="center" valign="top">17.2</td>
<td align="center" valign="top">3.2</td>
</tr>
<tr>
<td align="left" valign="top">Female children</td>
<td align="center" valign="top">14.1</td>
<td align="center" valign="top">1.9</td>
<td align="center" valign="top">15.3</td>
<td align="center" valign="top">2.2</td>
<td align="center" valign="top">17.2</td>
<td align="center" valign="top">2.7</td>
</tr>
<tr>
<td align="left" valign="top">Male adults</td>
<td align="center" valign="top">14.9</td>
<td align="center" valign="top">10.5</td>
<td align="center" valign="top">16.0</td>
<td align="center" valign="top">13.1</td>
<td align="center" valign="top">17.8</td>
<td align="center" valign="top">16.4</td>
</tr>
<tr>
<td align="left" valign="top">Female adults</td>
<td align="center" valign="top">14.9</td>
<td align="center" valign="top">9.6</td>
<td align="center" valign="top">16.0</td>
<td align="center" valign="top">12.0</td>
<td align="center" valign="top">17.7</td>
<td align="center" valign="top">15.1</td>
</tr>
<tr>
<td align="left" valign="top">Male elders</td>
<td align="center" valign="top">14.9</td>
<td align="center" valign="top">17.0</td>
<td align="center" valign="top">16.0</td>
<td align="center" valign="top">18.7</td>
<td align="center" valign="top">17.7</td>
<td align="center" valign="top">21.6</td>
</tr>
<tr>
<td align="left" valign="top">Female elders</td>
<td align="center" valign="top">14.9</td>
<td align="center" valign="top">15.7</td>
<td align="center" valign="top">16.0</td>
<td align="center" valign="top">17.3</td>
<td align="center" valign="top">17.7</td>
<td align="center" valign="top">20.0</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>&#x002A;NCR: Non-Carcinogenic Health Risks.</p>
<p>&#x002A;&#x002A;CR: Carcinogenic Health Risks.</p>
</table-wrap-foot>
</table-wrap>
<p>Non-carcinogenic health risks based on PM<sub>2.5</sub> annual reference standards are presented in <xref ref-type="table" rid="tab4">Table 4</xref>. Based on the annual PM<sub>2.5</sub> SA NAAQS, all population sub-groups in eMbalenhle showed 95th percentile HQ values below 1. Using the USEPA NAAQS, all population subgroups showed HQ values greater than 1, using the 50th, 75th and 95th percentiles of C<sub>air-adj</sub>. Throughout all the reference standards (WHO Guidelines, SA and US EPA NAAQS), the 50th, 75th and 95th HQ percentiles indicated varying health risks of exposure to PM<sub>2.5</sub> eMbalenhle. The WHO Guidelines showed the highest potential to curb non-carcinogenic risks, followed by USEPA and the SA NAAQS. When estimating the hazard quotient (HQ) for the 95th percentile of the SA NAAQS, the risk of developing non-carcinogenic health effects was four times lower than WHO&#x2019;s HQ. This difference indicates that using NAAQS to evaluate health risks could underestimate the risk for individuals exposed to PM<sub>2.5</sub> in eMbalenhle.</p>
<table-wrap position="float" id="tab4">
<label>Table 4</label>
<caption>
<p>Non-carcinogenic risk assessment of PM<sub>2.5</sub> among population sub-groups in eMbalenhle.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Population</th>
<th align="left" valign="top">Standard/guideline</th>
<th align="center" valign="top">Percentile</th>
<th align="center" valign="top">HQ</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="middle" rowspan="9">&#x002A;All Population Sub-groups (Male and Female Toddlers, Children, Adults, and Elders)</td>
<td align="left" valign="middle" rowspan="3">SA NAAQS</td>
<td align="center" valign="middle">50th</td>
<td align="center" valign="middle">0.7</td>
</tr>
<tr>
<td align="center" valign="middle">75th</td>
<td align="center" valign="middle">0.8</td>
</tr>
<tr>
<td align="center" valign="middle">95th</td>
<td align="center" valign="middle">0.9</td>
</tr>
<tr>
<td align="left" valign="middle" rowspan="3">USEPA</td>
<td align="center" valign="middle">50th</td>
<td align="center" valign="middle">1.7</td>
</tr>
<tr>
<td align="center" valign="middle">75th</td>
<td align="center" valign="middle">1.8</td>
</tr>
<tr>
<td align="center" valign="middle">95th</td>
<td align="center" valign="middle">2.0</td>
</tr>
<tr>
<td align="left" valign="middle" rowspan="3">WHO</td>
<td align="center" valign="middle">50th</td>
<td align="center" valign="middle">3.0</td>
</tr>
<tr>
<td align="center" valign="middle">75th</td>
<td align="center" valign="middle">3.2</td>
</tr>
<tr>
<td align="center" valign="middle">95th</td>
<td align="center" valign="middle">3.5</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p>&#x002A;The computed HQ values for each subpopulation group are the same based on the NCR values presented in <xref ref-type="table" rid="tab3">Table 3</xref>.</p>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="sec12">
<label>4.1.2</label>
<title>Carcinogenic risk assessment of exposure to PM<sub>2.5</sub> in eMbalenhle</title>
<p>The results in <xref ref-type="table" rid="tab5">Table 5</xref> and <xref ref-type="fig" rid="fig1">Figure 1</xref> report the CR for male and female age groups in eMbalenhle based on exposure to adjusted PM<sub>2.5</sub> related to their characteristics. For both male and female elders, the CR was approximately 1 in 10, meaning that about 100,000 out of 1,000,000 exposed elders were at an increased risk of developing cancer over their lifetime due to PM<sub>2.5</sub> exposure at the reported levels. Even for toddlers born and raised in eMbalenhle, the probability of developing cancer during their lifetime exceeds the critical 1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;04</sup> level.</p>
<table-wrap position="float" id="tab5">
<label>Table 5</label>
<caption>
<p>Carcinogenic human health risks of exposure to PM<sub>2.5</sub>.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Population sub-groups</th>
<th align="center" valign="top">50th-percentile</th>
<th align="center" valign="top">75th-percentile</th>
<th align="center" valign="top">95th-percentile</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="bottom">Male toddlers</td>
<td align="center" valign="bottom">3&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;3</sup></td>
<td align="center" valign="bottom">4&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;3</sup></td>
<td align="center" valign="bottom">4&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;3</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Female toddlers</td>
<td align="center" valign="bottom">3&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;3</sup></td>
<td align="center" valign="bottom">3&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;3</sup></td>
<td align="center" valign="bottom">4&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;3</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Male children</td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">3&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Female children</td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Male adults</td>
<td align="center" valign="bottom">8&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">10&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Female adults</td>
<td align="center" valign="bottom">7&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">10&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;2</sup></td>
<td align="center" valign="bottom">1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Male elders</td>
<td align="center" valign="bottom">1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
</tr>
<tr>
<td align="left" valign="bottom">Female elders</td>
<td align="center" valign="bottom">1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
<td align="center" valign="bottom">1&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
<td align="center" valign="bottom">2&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;1</sup></td>
</tr>
</tbody>
</table>
</table-wrap>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Maps showing the study area within the Country, Province, and District.</p>
</caption>
<graphic xlink:href="fpubh-13-1515009-g001.tif">
<alt-text content-type="machine-generated">Map illustrating Mpumalanga in South Africa with insets highlighting Gert Sibande and Govan Mbeki regions. The larger map shows areas including Secunda, Evander, and Bethal. A red boundary outlines Govan Mbeki, with monitoring stations marked. A compass indicates orientation.</alt-text>
</graphic>
</fig>
</sec>
<sec id="sec13">
<label>4.1.3</label>
<title>Sensitivity analysis of model inputs based on non-cancer and cancer risks</title>
<p>The contribution of input parameters to the variance in non-cancer risks is shown in <xref ref-type="fig" rid="fig2">Figures 2</xref>, <xref ref-type="fig" rid="fig3">3</xref>. The variation of C<sub>air</sub> showed the highest contribution to the variance in the non-cancer risk (72.4%, range of 57&#x2013;87%), whereas on average, ET and EF contributed 25.5% (range of 11&#x2013;41%) and 4% (range of 1&#x2013;7%), respectively to the variance in non-cancer risks.</p>
<fig position="float" id="fig2">
<label>Figure 2</label>
<caption>
<p>Sensitivity analysis of the parameters based on non-cancer risks.</p>
</caption>
<graphic xlink:href="fpubh-13-1515009-g002.tif">
<alt-text content-type="machine-generated">Bar chart titled "Hazard Quotient" with horizontal bars representing input parameters on the y-axis: EF, ET, and Cair. The x-axis shows percentages. EF is just above 0%, ET is around 30%, and Cair is close to 70%.</alt-text>
</graphic>
</fig>
<fig position="float" id="fig3">
<label>Figure 3</label>
<caption>
<p>Sensitivity analysis of the input parameters based on cancer risks.</p>
</caption>
<graphic xlink:href="fpubh-13-1515009-g003.tif">
<alt-text content-type="machine-generated">Bar graph titled "Cancer Risk" shows percent risk across population sub-groups categorized into male and female toddlers, children, adults, and elders. Variables include ED, Cair, AT, ET, and EF, represented by different colored bars. Male toddlers, female toddlers, male children, female children, male adults, and female adults have high ED values around 60%. Cair is significant for male and female elders. AT, ET, and EF values are comparatively low across groups.</alt-text>
</graphic>
</fig>
<p><xref ref-type="fig" rid="fig3">Figure 3</xref> shows that the parameter sensitivity for the variance in CR for the older adult subgroups deviates from the other age groups. The highest contributions to the CR variance for the older adult were the C<sub>air</sub> and the AT, whereas the ED showed the highest sensitivity for the other subgroups.</p>
</sec>
</sec>
</sec>
<sec sec-type="discussion" id="sec14">
<label>5</label>
<title>Discussion</title>
<p>This study reported an annual GM PM<sub>2.5</sub> concentration of 17&#x202F;&#x03BC;g/m<sup>3</sup>. Various PM<sub>2.5</sub> sources, including traffic emissions, industrial activities, domestic cooking, space heating, waste-burning and dust from gold mine TSFs, could have contributed to the increased levels of PM<sub>2.5</sub> in eMbalenhle. This annual concentration level was below the South African NAAQS of 20&#x202F;&#x03BC;g/m<sup>3</sup>. However, it exceeded the WHO air quality guidelines and the USEPA NAAQS of 5&#x202F;&#x03BC;g/m<sup>3</sup> and 9&#x202F;&#x03BC;g/m<sup>3</sup>, respectively. This indicated that although the local air quality standards are met, the exposed population may still experience significant health risks when the reported PM<sub>2.5</sub> concentrations are compared with international reference standards. The exceedances of international standards from February 2022 to February 2023 indicated a potential public health concern, especially for vulnerable population sub-groups living close to sources of PM<sub>2.5</sub> and gold mine TSFs. Although annual PM<sub>2.5</sub> emissions reported in this study are slightly below the SA NAAQS, Millar et al. (<xref ref-type="bibr" rid="ref65">65</xref>) that, for the past 10&#x202F;years (2009&#x2013;2019), the annual PM<sub>2.5</sub> concentrations in eMbalenhle exceeded the SA NAAQS each year. The study used high-resolution data from the South African Weather Service (SAWS) air quality monitoring station.</p>
<p>Different countries have varying ambient PM<sub>2.5</sub> NAAQSs. This is due to environmental, health, social, political and economic factors (<xref ref-type="bibr" rid="ref66">66</xref>) affecting these countries. The WHO (<xref ref-type="bibr" rid="ref51">51</xref>) provides guidelines for air quality, but countries adopt these recommendations differently based on their national circumstances. In most cases, developing countries may prioritize economic growth and industrialization over strict air quality standards to avoid limiting industrial expansion (<xref ref-type="bibr" rid="ref67">67</xref>). In contrast, developed countries may impose more stringent regulations to protect public health and the environment. Moreover, countries with advanced air quality management and monitoring technologies may set and enforce stricter NAAQS (<xref ref-type="bibr" rid="ref68">68</xref>). Countries with less technological capacity may set more lenient standards due to challenges in air quality monitoring (<xref ref-type="bibr" rid="ref69">69</xref>).</p>
<p>For the probalistic HHRA, the PM<sub>2.5</sub> concentrations were adjusted to reflect an accurate estimation of an equivalent full-day exposure over 1&#x202F;year in the eMbalenhle population. The results showed that the median (50th percentile) for non-carcinogenic risk was low (below 1) across all population subgroups based on SA NAAQS. However, compared to the more restrictive USEPA and WHO air quality guidelines, even the median HQ values demonstrated a substantially increased risk with HQ values of 1.5 and 2.8, respectively. Amnuaylojaroen and Parasin (<xref ref-type="bibr" rid="ref70">70</xref>) computed higher HQ values than this study. This is partly because they used RfC of 35&#x202F;&#x03BC;g/m<sup>3</sup> to calculate the HQ and worst-case assumptions regarding the risk parameters. The mean HQs were 2.93, 2.59, 2.28, 1.88, and 1.26 for newborns, toddlers, young children, school-age children, and adolescents, respectively.</p>
<p>Although the WHO air quality guidelines are widely adopted and used in many countries, they are not absolute and can be overly simplistic. First, the guidelines fail to account for cumulative risks and variability in individual susceptibility. Second, the guidelines fail to account for risk tolerance, which can vary between populations and regulatory bodies. Given this, there is a greater need to develop more robust and advanced approaches that factor in these issues to reflect real-world exposures accurately and avoid underestimating or overestimating risk.</p>
<p>For the cancer risk (CR), results showed values greater than 1.0&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;4</sup> (1 in 10,000) for all population subgroups, which is generally considered significant, calling for stricter regulatory action and interventions to prevent further exposure. For example, the 50th, 75th and 95th percentile values indicated significant CRs (all greater than 1.0&#x202F;&#x00D7;&#x202F;10<sup>&#x2212;4</sup>) across all population sub-groups. The CR became more significant in male and female elders. This result is similar to Wu et al. (<xref ref-type="bibr" rid="ref71">71</xref>), who found the CR more significant in male elders. In contrast, Stapelfeld et al. (<xref ref-type="bibr" rid="ref72">72</xref>) found that females were more at risk of developing cancer than males. In our study, the slightly higher CR for men was due to the lower life expectancy than women, but this difference is not statistically significant. Furthermore, males have different hormonal profiles compared to females (<xref ref-type="bibr" rid="ref73">73</xref>) and as they age, the risk of developing cancer increases (<xref ref-type="bibr" rid="ref74">74</xref>).</p>
<p>The female children showed the least chance of developing CR because of PM<sub>2.5</sub> exposure compared to the other groups. Our estimations were determined by the ED/AT ratio, which was the lowest for toddlers and the highest for elders. Since toddlers and children are young, their risk for developing cancer is reduced because they have less accumulated genetic mutations (<xref ref-type="bibr" rid="ref75">75</xref>). Contrary to this, Siegel et al. (<xref ref-type="bibr" rid="ref76">76</xref>) observed that pediatric cancers were more pronounced in male children than in females.</p>
<p>The sensitivity analysis indicated that C<sub>air</sub> and ET had the most significant impact on non-cancer risks. Since C<sub>air</sub> is measured, the estimates for ET are key for estimating the extent of non-cancer risk. These findings call for regulatory action and policies to reduce exposures, especially to vulnerable groups. Strategies could include promulgating stringent emission standards for petrochemical industries, power plants, coal mines and gold mines. Inside the community, there should be an advocation for the transition to cleaner fuels, energy-efficient cookstoves and renewable energy sources to mitigate combustion-related PM<sub>2.5</sub> emissions (<xref ref-type="bibr" rid="ref77">77</xref>). Other strategies could include the spatial resolution of air quality monitoring in the area by adopting low-cost sensors (<xref ref-type="bibr" rid="ref78">78</xref>), issuing early warnings for high pollution days (<xref ref-type="bibr" rid="ref79">79</xref>), and raising public awareness to empower communities to take protective measures. On the other hand, the ED was the most sensitive parameter for the CR due to the assumed uniform distribution in the adult subgroup. For the older adult, where the ED/AT ratio is close to one, the variation in C<sub>air</sub> becomes more significant for the estimates of the CR. In a similar study, Amoatey et al. (<xref ref-type="bibr" rid="ref80">80</xref>) observed that long durations of exposure to ambient PM<sub>2.5</sub> increased adverse health outcomes amongst the Roman population.</p>
<p>Applying the probabilistic HHRA model may be more complex than the deterministic approach (<xref ref-type="bibr" rid="ref81">81</xref>). The determinist HHRA approach uses fixed point estimates for input variables (ED, ET, EF, AT) (<xref ref-type="bibr" rid="ref82">82</xref>). Often, the maximum values are used, resulting in worst-case assessments. In contrast, the probabilistic HHRA uses probability distributions for input variables to account for variability and uncertainty (<xref ref-type="bibr" rid="ref83">83</xref>). Amnuaylojaroen and Parasin (<xref ref-type="bibr" rid="ref70">70</xref>) applied a deterministic risk assessment model to assess the health impacts of exposure to PM<sub>2.5</sub> in different age groups of children in Northern Thailand. Compared to the probabilistic HHRA model that was applied in this study, their model considered the body weight and inhalation rate as variables, as also in Morakinyo et al. (<xref ref-type="bibr" rid="ref84">84</xref>). The study also postulated that PM<sub>2.5</sub> exposure might affect children differently depending on gender, with males at a higher risk than females in adolescence (<xref ref-type="bibr" rid="ref70">70</xref>).</p>
</sec>
<sec sec-type="conclusions" id="sec15">
<label>6</label>
<title>Conclusion</title>
<p>The findings of the study demonstrated that the SA NAAQS may not adequately protect public health as it may underestimate the risks associated with PM<sub>2.5</sub>. To protect public health, there is a need for the government to adopt more stringent standards and align them closely with international standards, including the WHO guidelines.</p>
<p>Using a probabilistic human health risk assessment (HHRA) approach, the study revealed that non-carcinogenic risks were low when benchmarked against the SA NAAQS, but substantially elevated when compared with international guidelines. Vulnerable groups, particularly newborns and toddlers, exhibited higher hazard quotients (HQs), underscoring their increased susceptibility. For cancer risks (CR), results exceeded the generally acceptable threshold of 1 in 10,000 across all population groups, particularly affecting the older adult.</p>
<p>PM<sub>2.5</sub> concentrations were the most significant factor in increased non-cancer health problems in all sub-population groups. This emphasizes the need for control measures to reduce PM<sub>2.5</sub> concentrations, including the maintenance of TSFs and increasing monitoring in hot spot areas. The ED was the most critical factor for the cancer risks, followed by the air concentration for all population sub-groups except for the older adult. Strategies to reduce the ED and EF, such as limiting outdoor activities during high pollution events could further minimize health risks associated with exposure to PM<sub>2.5</sub>. The sensitivity analysis indicated that ambient PM<sub>2.5</sub> concentration (C<sub>air</sub>) and exposure time (ET) had the most influence on non-cancer risk estimates, while exposure duration (ED) was key for cancer risks. These observations indicate the urgent need for targeted interventions to minimize exposure, especially among vulnerable populations. Policy actions could include tighter emissions controls, community-level interventions to promote dust control alternatives, TSF management strategies, and expanded air quality monitoring networks using low-cost sensors.</p>
<p>Considering the above, this study calls for an urgent review of the current South African NAAQS. However, policymakers should strike a good and functional balance between economic imperatives and public health outcomes. Even though the WHO provides global benchmarks, countries can adopt these to meet their socio-economic context, technological feasibility and regulatory frameworks.</p>
</sec>
<sec id="sec16">
<label>7</label>
<title>Study limitations</title>
<p>The LCM measurement results over the year represent the temporal variations; however, spatial variations were not covered, limiting the representativeness of the PM<sub>2.5</sub> concentration data for the general population of eMbalenhle. In addition to this measured parameter (C<sub>air</sub>), the HQ and CR risk equations, distribution and values for all other parameters, except life expectancy, were only estimates and not based on actual data or information from the community. In-depth population studies are needed to collect more relevant information, especially for the highest sensitivity risk parameters. Therefore, this study&#x2019;s HQ and CR probability distributions can only be considered to flag potential health risks for the eMbalenhle residents. Lastly, this study made assumptions for the ED and EF for all population subgroups. This can limit the reliability and generalizability of the findings, as these parameters may not accurately reflect the diverse exposure patterns across the population subgroups. Uniform distribution patterns and assumptions of uniform exposure may overlook important activity data, including age-specific behaviours and varying susceptibility. This could lead to potential underestimation or overestimation of risks.</p>
</sec>
</body>
<back>
<sec sec-type="data-availability" id="sec17">
<title>Data availability statement</title>
<p>The raw data supporting the conclusions of this article will be made available by the authors without undue reservation.</p>
</sec>
<sec sec-type="author-contributions" id="sec18">
<title>Author contributions</title>
<p>NT: Conceptualization, Data curation, Formal analysis, Methodology, Software, Validation, Writing &#x2013; original draft, Writing &#x2013; review &#x0026; editing. TM: Supervision, Writing &#x2013; review &#x0026; editing. DM: Supervision, Writing &#x2013; review &#x0026; editing. DB: Formal analysis, Supervision, Methodology, Writing &#x2013; review &#x0026; editing.</p>
</sec>
<sec sec-type="funding-information" id="sec19">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. This study was funded under the Masters and Doctoral Support Programme (MDSP) of the University of South Africa (UNISA).</p>
</sec>
<ack>
<p>We want to thank Dr. G. Keretetse for assisting with the training on how to run the simulation model.</p>
</ack>
<sec sec-type="COI-statement" id="sec20">
<title>Conflict of interest</title>
<p>The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
</sec>
<sec sec-type="ai-statement" id="sec21">
<title>Generative AI statement</title>
<p>The authors declare that Gen AI was used in the creation of this manuscript. AI was used to improve the language and grammar.</p>
</sec>
<sec sec-type="disclaimer" id="sec22">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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<app-group>
<app id="app1">
<title>Appendix A: sensitivity analysis for population sub-groups in eMbalenhle</title>
<fig position="float" id="fig4">
<label>Figure A1</label>
<caption>
<p>Sensitivity analysis of the parameters based on non-cancer risks in eMbalenhle.</p>
</caption>
<graphic xlink:href="fpubh-13-1515009-g004.tif">
<alt-text content-type="machine-generated">Bar chart titled "Hazard Quotient" showing different population sub-groups on the y-axis: Female Elders, Male Elders, Female Adults, Male Adults, Female Child, Male Child, Female Toddlers, and Male Toddlers. The x-axis represents hazard quotient in percentages from 0 to 100. Each sub-group has three color-coded bars: gray for EF, orange for ET, and blue for Cair, with various lengths indicating different hazard levels for each parameter.</alt-text>
</graphic>
</fig>
</app>
</app-group>
</back>
</article>