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  <front>
    <journal-meta><journal-id journal-id-type="publisher">ACP</journal-id><journal-title-group>
    <journal-title>Atmospheric Chemistry and Physics</journal-title>
    <abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title><abbrev-journal-title abbrev-type="nlm-ta">Atmos. Chem. Phys.</abbrev-journal-title>
  </journal-title-group><issn pub-type="epub">1680-7324</issn><publisher>
    <publisher-name>Copernicus Publications</publisher-name>
    <publisher-loc>Göttingen, Germany</publisher-loc>
  </publisher></journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.5194/acp-25-13007-2025</article-id><title-group><article-title>Different response characteristics of ambient  hazardous trace metals and health impacts  to global emission reduction</article-title><alt-title>Global emission reduction generated marked health benefits</alt-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author" equal-contrib="yes" corresp="no" rid="aff1 aff2 aff3">
          <name><surname>Sun</surname><given-names>Wenwen</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-6960-6989</ext-link></contrib>
        <contrib contrib-type="author" equal-contrib="yes" corresp="no" rid="aff4">
          <name><surname>Liu</surname><given-names>Xing</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="yes" rid="aff5">
          <name><surname>Li</surname><given-names>Rui</given-names></name>
          <email>rli@geo.ecnu.edu.cn</email>
        </contrib>
        <aff id="aff1"><label>1</label><institution>Department of Research, Shanghai University of Medicine &amp; Health Sciences Affiliated Zhoupu Hospital, Shanghai 201318, China</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention (LAP<sup>3</sup>), Department of Environmental Science and Engineering, Fudan University, Shanghai 200433, China</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>College of Medical Technology, Shanghai University of Medicine &amp; Health Sciences, Shanghai 201318, China</institution>
        </aff>
        <aff id="aff4"><label>4</label><institution>State Environmental Protection Key Laboratory of Coastal Ecosystem, National Marine Environmental Monitoring Center, Dalian 116023, China</institution>
        </aff>
        <aff id="aff5"><label>5</label><institution>Key Laboratory of Geographic Information Science of the Ministry of Education, School of Geographic Sciences, East China Normal University, Shanghai 200241, China</institution>
        </aff><author-comment content-type="econtrib"><p>These authors contributed equally to this work.</p></author-comment>
      </contrib-group>
      <author-notes><corresp id="corr1">Rui Li (rli@geo.ecnu.edu.cn)</corresp></author-notes><pub-date><day>20</day><month>October</month><year>2025</year></pub-date>
      
      <volume>25</volume>
      <issue>20</issue>
      <fpage>13007</fpage><lpage>13018</lpage>
      <history>
        <date date-type="received"><day>5</day><month>May</month><year>2025</year></date>
           <date date-type="accepted"><day>28</day><month>August</month><year>2025</year></date>
           <date date-type="rev-recd"><day>12</day><month>August</month><year>2025</year></date>
           <date date-type="rev-request"><day>2</day><month>June</month><year>2025</year></date>
      </history>
      <permissions>
        <copyright-statement>Copyright: © 2025 Wenwen Sun et al.</copyright-statement>
        <copyright-year>2025</copyright-year>
      <license license-type="open-access"><license-p>This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link></license-p></license></permissions><self-uri xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025.html">This article is available from https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025.html</self-uri><self-uri xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025.pdf">The full text article is available as a PDF file from https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025.pdf</self-uri>
      <abstract><title>Abstract</title>

      <p id="d2e136">Airborne hazardous trace metals pose significant risks to human health. However, the response characteristics of ambient trace metals to emission reductions remain poorly understood. The COVID-19 pandemic offered a unique opportunity to investigate these response mechanisms and optimize emission control strategies. In this study, we employed the Global Modeling System for Chemistry (GEOS-Chem) chemical transport model to predict global variations in atmospheric concentrations of nine hazardous trace metals (As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn) and assess their responses to COVID-19 lockdown measures. Our results revealed that global average concentrations of As, Cd, Cr, Cu, Mn, Ni, and V decreased by 1 %–7 %, whereas Pb and Zn levels increased by 0.4 % and 2 %, respectively. The rise in Pb and Zn concentrations during lockdowns was primarily linked to sustained coal combustion and non-ferrous smelting activities, which remained essential for residential energy demands. Spatially, India, Western Europe (WE), and North America (NA) experienced the most pronounced declines in trace metal levels, while Sub-Saharan Africa (SS) and Australia showed minimal sensitivity to lockdown-induced emission reductions. Based on the scenario analysis, we found the concentrations of trace metals displayed linear response to emission reduction. Combined with the health risk assessment, we demonstrated the reduced emissions of Pb and As during the lockdown period yielded the greatest health benefits – Pb reductions were associated with lower non-carcinogenic risks, while As declines contributed most significantly to reduced carcinogenic risks. Targeting fossil fuel combustion should be prioritized in Pb and As mitigation strategies.</p>
  </abstract>
    
<funding-group>
<award-group id="gs1">
<funding-source>National Natural Science Foundation of China</funding-source>
<award-id>U23A2030</award-id>
</award-group>
</funding-group>
</article-meta>
  </front>
<body>
      

<sec id="Ch1.S1" sec-type="intro">
  <label>1</label><title>Introduction</title>
      <p id="d2e148">With the rapid advancement of industrial development and urbanization, numerous hazardous trace metals have been released into the atmosphere (Cheng et al., 2015; Yu et al., 2012; Zhu et al., 2020). These toxic elements injected into the air can negatively impact terrestrial and aquatic ecosystems through dry or wet deposition and pose significant risks to human health through long-term exposure (Al-Sulaiti et al., 2022; Pan and Wang, 2015; Sharma et al., 2023). Certain trace elements, including arsenic (As), cadmium (Cd), chromium (Cr), and lead (Pb), have been classified as carcinogens by the International Agency for Research on Cancer (IARC) (Bai et al., 2023; Loomis et al., 2018; Pearce et al., 2015). Therefore, it is crucial to investigate the spatiotemporal characteristics of hazardous trace metals in the atmosphere and assess their health impacts. Such efforts are instrumental in identifying hotspots and formulating effective control measures to mitigate health risks.</p>
      <p id="d2e151">A growing body of studies have explored the long-term trends of ambient trace elements in various cities (Das et al., 2023; Guo et al., 2022; Nirmalkar et al., 2021). For example, Farahani et al. (2021) reported significant decreases in <inline-formula><mml:math id="M1" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">PM</mml:mi><mml:mn mathvariant="normal">2.5</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>-bound levels of nickel (Ni), vanadium (V), zinc (Zn), lead (Pb), manganese (Mn), and copper (Cu) in central Los Angeles between 2005 and 2018 (Farahani et al., 2021). Although some studies have analyzed the long-term trends of ambient hazardous trace metals in specific regions, the spatiotemporal variations in most areas remain poorly understood due to the limited spatial representativeness of monitoring sites. To address these limitations, some researchers have utilized chemical transport models to predict regional or global concentrations of ambient hazardous trace metals. For instance, Liu et al. (2021) employed the Community Multiscale Air Quality (CMAQ) model to estimate the concentrations of 11 trace elements and found that most of these elements exhibited higher levels in the North China Plain (NCP). Additionally, Zhang et al. (2020) used the GEOS-Chem model to predict global ambient arsenic (As) concentrations from 2005 to 2015. Their findings revealed that atmospheric As levels in India exceeded those in eastern China, primarily due to the sharp increase in coal combustion across India. However, to date, the spatiotemporal variations of multiple hazardous trace metals on a global scale remain poorly understood. Moreover, the response of ambient trace elements to changes in emissions is still unknown. Bridging this knowledge gap is crucial for implementing effective control and prevention measures targeted at specific trace elements.</p>
      <p id="d2e165">COVID-19 swept across the globe between January and April 2020 (da Fonseca et al., 2021; Saadat et al., 2020; Venter et al., 2020). To prevent the rapid spread of this complex disease, many strict lockdown measures such as lockdown were implemented (Meo et al., 2020; Onyeaka et al., 2021; Xing et al., 2021). These stringent control measures led to dramatic decreases in the levels of many gaseous precursors, such as <inline-formula><mml:math id="M2" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">NO</mml:mi><mml:mi>x</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> and CO. Keller et al. (2021) estimated that global <inline-formula><mml:math id="M3" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">NO</mml:mi><mml:mi>x</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> emissions were reduced by 3.1 <inline-formula><mml:math id="M4" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">Tg</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mi mathvariant="normal">N</mml:mi></mml:mrow></mml:math></inline-formula> during January–June 2020, accounting for 5.5 % of total anthropogenic emissions. Although the impacts of COVID-19 lockdown on multiple pollutants have been explored, the response of ambient hazardous trace metals to emission changes and the emission reduction thresholds during the COVID-19 period still remained unknown. Additionally, the separate contributions of emission reductions and meteorological factors to ambient hazardous trace metal levels are also unclear. The COVID-19 pandemic provided an unprecedented opportunity to uncover these response mechanisms and marginal benefits of emission reduction, offering valuable insights for developing effective air pollution mitigation strategies.</p>
      <p id="d2e201">Here, we developed a new trace metal emission inventory and employed the GEOS-Chem model to predict the global variations of ambient trace elements before and during the COVID-19 period. First, we analyzed the spatiotemporal variations of ambient trace metal levels. Then, we distinguished the contributions of emission changes and meteorology. Finally, we quantified the health benefits resulting from emission reductions. Our study provides valuable insights and targeted policy implications for future air pollution control.</p>
</sec>
<sec id="Ch1.S2">
  <label>2</label><title>Materials and methods</title>
<sec id="Ch1.S2.SS1">
  <label>2.1</label><title>Overview</title>
      <p id="d2e219">The workflow of our methodology is depicted in Fig. S2. At first, we developed a global trace metal emission inventory based on activity levels and emission factors. Then, we incorporated the global emission inventory into the chemical transport model to estimate the global trace metal concentrations during 2017–2020. The parametrization scheme of chemical transport model was configured based on the ground-level observations. The optimal scheme was set up to obtain the accurate spatial maps of global trace metal concentrations. At last, we assessed the health risks associated with the trace metal exposures during this period.</p>
</sec>
<sec id="Ch1.S2.SS2">
  <label>2.2</label><title>The global emission inventory of hazardous trace metals</title>
      <p id="d2e230">According to the classification standard proposed by Streets et al. (2011), all countries and regions worldwide could be categorized into five groups, ranging from the most developed (Region 1) to the least developed (Region 5). Anthropogenic emission factors and the removal efficiency of hazardous trace metals vary significantly among these regions. Detailed data were obtained from Tables S1–S9 in the Supplement. Coal combustion sources were further divided into two subcategories: coal-fired power plants and other coal-fired sectors. Non-coal combustion sources were classified into six subsectors: liquid fuel combustion, ferrous metal smelting, non-ferrous metal smelting, non-metallic mineral manufacturing, vehicle emissions, and municipal solid waste incineration. Natural emissions, including those from dust, biomass burning, and sea salt (Tables S10–S13), were estimated in detail using the methodology described by Wu et al. (2020). Based on these categorizations and methodologies, an emission inventory for nine trace metals including As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn was developed. The detailed emission inventory description was introduced in the Supplement (Sects. S1 and S2).</p>
</sec>
<sec id="Ch1.S2.SS3">
  <label>2.3</label><title>Ground-level observations</title>
      <p id="d2e241">Most of the ground-level ambient hazardous trace metal observations (<inline-formula><mml:math id="M5" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">PM</mml:mi><mml:mn mathvariant="normal">10</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>) mainly focused on China, Western Europe, and Contiguous United States. China did not possess regular ground-level observations of ambient trace metals, and thus we only collected these data from previous references. Both of Western Europe and Contiguous United States possessed regular ambient trace metal observations. The European Monitoring and Evaluation Programme (EMEP) comprises of more than 100 sites about trace metal observations across Europe in past 20 years. The quality control of EMEP was explained by Tørseth et al. (2012). The dataset of daily ambient trace metal concentrations in many sites across the United States were downloaded from the website of <uri>https://www.epa.gov/</uri> (last access: 5 May 2025) (Fig. S1 and Table S14 in the Supplement).</p>
</sec>
<sec id="Ch1.S2.SS4">
  <label>2.4</label><title>GEOS-Chem model</title>
      <p id="d2e266">The GEOS-Chem model (v12-01) was utilized to simulate the concentration differences of nine hazardous trace metals in the atmosphere during the period from 23 January to 30 April, comparing 2020 to 2017–2019. These differences were attributed to the combined effects of emission changes and meteorological variations. The core mechanism of this model integrates tropospheric <inline-formula><mml:math id="M6" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">NO</mml:mi><mml:mi>x</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>-VOC-<inline-formula><mml:math id="M7" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>-aerosol chemistry (Mao et al., 2010; Park et al., 2004). In our study, we treated the deposition processes of trace metals similarly as aerosol particles because most (90 % or more) atmospheric trace metals sorb onto aerosols especially fine-mode (i.e., <inline-formula><mml:math id="M8" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">PM</mml:mi><mml:mn mathvariant="normal">2.5</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>) aerosols. Furthermore, the trace metals were generally considered to be inert, and thus the chemical reactions were not added in the trace metal modelling. Only physical processed such as emission, mixing, transport, and depositions were considered in the model. Wet deposition processes include sub-grid scavenging in convective updrafts, in-cloud rainout, and below-cloud washout (Liu et al., 2001). Dry deposition was calculated using a resistance-in-series model (Wesely, 2007). The model was driven by meteorological data assimilated from the MERRA2 reanalysis (Qiu et al., 2020). A global simulation at a 2° <inline-formula><mml:math id="M9" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 2.5° resolution was conducted to estimate the concentrations of hazardous trace metals on a global scale (Qiu et al., 2020). Anthropogenic trace metal emission inventories for 2017–2019 and 2020 were derived from Sect. <xref ref-type="sec" rid="Ch1.S2.SS1"/>, while natural emissions included dust, biomass burning, and sea salt. The modelled trace metal concentration is the sum of trace metal concentrations in particle sizes <inline-formula><mml:math id="M10" display="inline"><mml:mo>≤</mml:mo></mml:math></inline-formula> 5 <inline-formula><mml:math id="M11" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi><mml:mi mathvariant="normal">m</mml:mi></mml:mrow></mml:math></inline-formula> in diameter (accumulation mode) and particle sizes between 2.5 and 10 <inline-formula><mml:math id="M12" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi><mml:mi mathvariant="normal">m</mml:mi></mml:mrow></mml:math></inline-formula> in diameter (coarse mode). Model performance was evaluated using several statistical indicators, with the detailed equations provided in the Supplement (SI).</p>
      <p id="d2e339">To isolate the effects of emission reductions and meteorological changes on ambient hazardous trace metals, simulations using the 2017–2019 emission inventory and 2020 meteorological conditions (<inline-formula><mml:math id="M13" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mrow><mml:mn mathvariant="normal">2017</mml:mn><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2019</mml:mn><mml:mi mathvariant="normal">emi</mml:mi><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2020</mml:mn><mml:mi mathvariant="normal">met</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>) were also conducted. <inline-formula><mml:math id="M14" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mn mathvariant="normal">2020</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> and <inline-formula><mml:math id="M15" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mrow><mml:mn mathvariant="normal">2017</mml:mn><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2019</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula> represent simulation results based on the emissions and meteorological conditions of 2020 and 2017–2019, respectively. The pollutant concentration differences between 2017–2019 and 2020 caused by emissions (<inline-formula><mml:math id="M16" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mi mathvariant="normal">emi</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>) and meteorology (<inline-formula><mml:math id="M17" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mi mathvariant="normal">met</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>) were quantified using the following equations:

                <disp-formula specific-use="align" content-type="numbered"><mml:math id="M18" display="block"><mml:mtable displaystyle="true"><mml:mlabeledtr id="Ch1.E1"><mml:mtd><mml:mtext>1</mml:mtext></mml:mtd><mml:mtd><mml:mstyle displaystyle="true" class="stylechange"/></mml:mtd><mml:mtd><mml:mrow><mml:mstyle class="stylechange" displaystyle="true"/><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mi mathvariant="normal">emi</mml:mi></mml:msub></mml:mrow><mml:mo>=</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mn mathvariant="normal">2020</mml:mn></mml:msub></mml:mrow><mml:mo>-</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mrow><mml:mn mathvariant="normal">2017</mml:mn><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2019</mml:mn><mml:mi mathvariant="normal">emi</mml:mi><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2020</mml:mn><mml:mi mathvariant="normal">met</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:mtd></mml:mlabeledtr><mml:mlabeledtr id="Ch1.E2"><mml:mtd><mml:mtext>2</mml:mtext></mml:mtd><mml:mtd><mml:mstyle displaystyle="true" class="stylechange"/></mml:mtd><mml:mtd><mml:mrow><mml:mstyle displaystyle="true" class="stylechange"/><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mi mathvariant="normal">met</mml:mi></mml:msub></mml:mrow><mml:mo>=</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mrow><mml:mn mathvariant="normal">2017</mml:mn><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2019</mml:mn><mml:mi mathvariant="normal">emi</mml:mi><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2020</mml:mn><mml:mi mathvariant="normal">met</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>-</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mrow><mml:mn mathvariant="normal">2017</mml:mn><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2019</mml:mn></mml:mrow></mml:msub></mml:mrow><mml:mo>.</mml:mo></mml:mrow></mml:mtd></mml:mlabeledtr></mml:mtable></mml:math></disp-formula></p>
      <p id="d2e516">The detailed calculation process is as follows. First, the concentrations of ambient trace metals for both 2017–2019 and 2020 were simulated. In the second step, the meteorology for 2020 was fixed, and the emission inventory was adjusted to 2017–2019 to calculate <inline-formula><mml:math id="M19" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mrow><mml:mn mathvariant="normal">2019</mml:mn><mml:mi mathvariant="normal">emi</mml:mi><mml:mtext>–</mml:mtext><mml:mn mathvariant="normal">2020</mml:mn><mml:mi mathvariant="normal">met</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>. The simulated ambient trace metal levels for 2020 were then subtracted from the simulated concentrations with 2017–2019 emissions and 2020 meteorology (Eq. <xref ref-type="disp-formula" rid="Ch1.E1"/>) to determine the contribution of emissions to the total difference in ambient trace metals during the COVID-19 period (<inline-formula><mml:math id="M20" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mi mathvariant="normal">emi</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>). Similarly, based on Eq. (<xref ref-type="disp-formula" rid="Ch1.E2"/>), the same method was applied to estimate the contribution of meteorology to the total difference in ambient trace metals during the COVID-19 period (<inline-formula><mml:math id="M21" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">GC</mml:mi><mml:mi mathvariant="normal">met</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula>). Different regions exerted lockdown measures during different periods. The lockdown periods in various regions were collected from <uri>https://en.wikipedia.org/wiki/COVID-19_pandemic_lockdowns</uri> (last access: 20 May 2025) (Keller et al., 2021). Five scenarios including base, 20 %_reduction, 40 %_reduction, 60 %_reduction, and 80 %_reduction were set up to assess the response of trace metal concentrations to emission change. For example, the 20 %_reduction means the global trace metal emission experienced 20 % reduction. In our study, the trace metal concentrations in eight major study regions including China, India, Western Europe (WE), North America (NA), South America (SA), Sub-Sahara Africa (SS), Russia, and Australia were simulated and further analyzed.</p>
</sec>
<sec id="Ch1.S2.SS5">
  <label>2.5</label><title>Health risk assessment model</title>
      <p id="d2e578">In this study, the carcinogenic and non-carcinogenic risks associated with hazardous trace metals in aerosols were evaluated using statistical thresholds established by IARC. Based on the IARC classification, trace metals such as As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn are identified as potentially carcinogenic to humans (Marufi et al., 2024; Tikadar et al., 2024). The risks of exposure to these hazardous trace metals were assessed for both adults (<inline-formula><mml:math id="M22" display="inline"><mml:mo lspace="0mm">≥</mml:mo></mml:math></inline-formula> 24 years old) and children (<inline-formula><mml:math id="M23" display="inline"><mml:mo lspace="0mm">&lt;</mml:mo></mml:math></inline-formula> 6 years old) using carcinogenic risk (CR) and hazard quotient (HQ) metrics. Both CR and HQ were derived from the average daily dose (ADD). The formulas used to calculate ADD, CR, and HQ were adopted from Kan et al. (2021) and Zhang et al. (2021) (Tables S15 and S16):

                <disp-formula specific-use="align" content-type="numbered"><mml:math id="M24" display="block"><mml:mtable displaystyle="true"><mml:mlabeledtr id="Ch1.E3"><mml:mtd><mml:mtext>3</mml:mtext></mml:mtd><mml:mtd><mml:mstyle displaystyle="true" class="stylechange"/></mml:mtd><mml:mtd><mml:mrow><mml:mstyle displaystyle="true" class="stylechange"/><mml:mtext>ADD</mml:mtext><mml:mo>=</mml:mo><mml:mo>(</mml:mo><mml:mi>C</mml:mi><mml:mo>×</mml:mo><mml:mtext>InhR</mml:mtext><mml:mo>×</mml:mo><mml:mtext>EF</mml:mtext><mml:mo>×</mml:mo><mml:mtext>ED</mml:mtext><mml:mo>)</mml:mo><mml:mo>/</mml:mo><mml:mo>(</mml:mo><mml:mtext>BW</mml:mtext><mml:mo>×</mml:mo><mml:mtext>AT</mml:mtext><mml:mo>)</mml:mo></mml:mrow></mml:mtd></mml:mlabeledtr><mml:mlabeledtr id="Ch1.E4"><mml:mtd><mml:mtext>4</mml:mtext></mml:mtd><mml:mtd><mml:mstyle displaystyle="true" class="stylechange"/></mml:mtd><mml:mtd><mml:mrow><mml:mstyle class="stylechange" displaystyle="true"/><mml:mtext>HQ</mml:mtext><mml:mo>=</mml:mo><mml:mtext>ADD</mml:mtext><mml:mo>/</mml:mo><mml:mtext>RfD</mml:mtext></mml:mrow></mml:mtd></mml:mlabeledtr><mml:mlabeledtr id="Ch1.E5"><mml:mtd><mml:mtext>5</mml:mtext></mml:mtd><mml:mtd><mml:mstyle displaystyle="true" class="stylechange"/></mml:mtd><mml:mtd><mml:mrow><mml:mstyle displaystyle="true" class="stylechange"/><mml:mtext>CR</mml:mtext><mml:mtext> =  ADD</mml:mtext><mml:mo>×</mml:mo><mml:mtext>CSF</mml:mtext></mml:mrow></mml:mtd></mml:mlabeledtr></mml:mtable></mml:math></disp-formula>

          where <inline-formula><mml:math id="M25" display="inline"><mml:mi>C</mml:mi></mml:math></inline-formula> (<inline-formula><mml:math id="M26" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">mg</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) represents the concentration of hazardous trace metals in the atmosphere, whereas InhR denotes the respiratory rate (<inline-formula><mml:math id="M27" display="inline"><mml:mrow class="unit"><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">d</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) (Table S15). EF refers to the exposure frequency (day), ED is the exposure duration (years), BW represents the average body weight (<inline-formula><mml:math id="M28" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi></mml:mrow></mml:math></inline-formula>), and AT is the average exposure time (days). ADD indicates the average daily intake (<inline-formula><mml:math id="M29" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">mg</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">kg</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">d</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) of hazardous trace metals, RfD is the reference dose (<inline-formula><mml:math id="M30" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">mg</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">kg</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">d</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) derived from reference concentrations, and CSF is the cancer slope factor (<inline-formula><mml:math id="M31" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="normal">d</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">mg</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) (Table S16). The potential non-carcinogenic risk of hazardous trace metals is considered high if the hazard quotient (HQ) exceeds 1.0, indicating significant health concerns. Conversely, an HQ below 1.0 suggests negligible health risks. The carcinogenic risk (CR) of each hazardous trace metal is assessed as significant if CR exceeds 10<sup>−4</sup>.</p>

      <fig id="F1" specific-use="star"><label>Figure 1</label><caption><p id="d2e820">The predictive accuracy of nine trace metals including As <bold>(a)</bold>, Cd <bold>(b)</bold>, Cr <bold>(c)</bold>, Cu <bold>(d)</bold>, Mn <bold>(e)</bold>, Ni <bold>(f)</bold>, Pb <bold>(g)</bold>, V <bold>(h)</bold>, and Zn <bold>(i)</bold> at the global scale based on GEOS-Chem model (Unit: <inline-formula><mml:math id="M33" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ng</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>).</p></caption>
          <graphic xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025-f01.png"/>

        </fig>

</sec>
</sec>
<sec id="Ch1.S3">
  <label>3</label><title>Results and discussions</title>
<sec id="Ch1.S3.SS1">
  <label>3.1</label><title>Model evaluation</title>
      <p id="d2e887">Initially, the GEOS-Chem model was employed to estimate ambient trace metal concentrations at the global scale. The correlation coefficients (R values) between the simulated and observed values for As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn were 0.79, 0.81, 0.81, 0.78, 0.79, 0.81, 0.83, 0.78, and 0.79 (Fig. <xref ref-type="fig" rid="F1"/>), respectively. The root mean square errors (RMSE) for As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn were 2.57, 4.43, 4.84, 11.0, 12.7, 3.64, 28.1, 9.33, and 30.1 <inline-formula><mml:math id="M34" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ng</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>, respectively. The mean absolute errors (MAE) for these trace metals were 0.94, 2.88, 2.15, 5.48, 6.73, 1.60, 12.3, 4.09, and 13.5 <inline-formula><mml:math id="M35" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ng</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>, respectively. Only Ni and V were overestimated, while the concentrations of most other trace metals were slightly underestimated. The predictive <inline-formula><mml:math id="M36" display="inline"><mml:mi>R</mml:mi></mml:math></inline-formula> values in our study were generally higher than those reported by Liu et al. (2021), with the exception of Mn (<inline-formula><mml:math id="M37" display="inline"><mml:mi>R</mml:mi></mml:math></inline-formula> <inline-formula><mml:math id="M38" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.87) and Cu (<inline-formula><mml:math id="M39" display="inline"><mml:mi>R</mml:mi></mml:math></inline-formula> <inline-formula><mml:math id="M40" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.86). It is likely that Liu et al. (2021) simulated ambient trace metal concentrations specifically in China, which experiences some of the most severe trace metal pollution globally. As a result, the simulated values in China were often underestimated. In contrast, our study conducted global simulations, which helped avoid such significant underestimation. Additionally, the predictive accuracy for ambient As concentrations in our study was higher than that of Zhang et al. (2020) (<inline-formula><mml:math id="M41" display="inline"><mml:mi>R</mml:mi></mml:math></inline-formula> <inline-formula><mml:math id="M42" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> 0.69). Overall, the predictive accuracy of ambient trace metal concentrations in our study was satisfactory, allowing us to use these data to further analyze the spatiotemporal characteristics of trace metal distributions.</p>

      <fig id="F2" specific-use="star"><label>Figure 2</label><caption><p id="d2e972">The global difference of trace element concentrations between January–April during 2017-2-019 and 2020. Nine trace elements including As <bold>(a)</bold>, Cd <bold>(b)</bold>, Cr <bold>(c)</bold>, Cu <bold>(d)</bold>, Mn <bold>(e)</bold>, Ni <bold>(f)</bold>, Pb <bold>(g)</bold>, V <bold>(h)</bold>, and Zn <bold>(i)</bold> were selected to analyze the annual variations (Unit: <inline-formula><mml:math id="M43" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ng</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>).</p></caption>
          <graphic xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025-f02.png"/>

        </fig>

</sec>
<sec id="Ch1.S3.SS2">
  <label>3.2</label><title>The concentration differences of ambient trace metals</title>
      <p id="d2e1031">Based on the simulated results, the global average concentrations of ambient As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn during January–April in 2017–2019 (2020) were 0.05 (0.04), 0.02 (0.02), 0.13 (0.12), 0.41 (0.37), 0.22 (0.20), 0.17 (0.16), 0.84 (0.83), 0.25 (0.22), and 0.43 (0.44) <inline-formula><mml:math id="M44" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ng</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula> (Figs. <xref ref-type="fig" rid="F2"/> and S2–S4), respectively. Most trace metals in the atmosphere experienced decreases during the COVID-19 period in 2020 compared to the “business-as-usual” period during 2017–2019. The global average concentrations of ambient As, Cd, Cr, Cu, Mn, Ni, and V decreased by 8 %, 1 %, 4 %, 7 %, 9 %, 6 %, and 10 %, respectively. However, global average concentrations of particulate Pb and Zn exhibited slight increases of 0.4 % and 2 %, respectively, during the same period.</p>

      <fig id="F3" specific-use="star"><label>Figure 3</label><caption><p id="d2e1052">The violin graphs of nine trace elements including As <bold>(a)</bold>, Cd <bold>(b)</bold>, Cr <bold>(c)</bold>, Cu <bold>(d)</bold>, Mn <bold>(e)</bold>, Ni <bold>(f)</bold>, Pb <bold>(g)</bold>, V <bold>(h)</bold>, and Zn <bold>(i)</bold> in eight major regions during January–April in 2020. Chi, Ind, WE, NA, SA, SS, Rus, and Aus represent China, India, Western Europe, North America, South America, Sub-Sahara Africa, Russia, and Australia, respectively.</p></caption>
          <graphic xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025-f03.png"/>

        </fig>

      <p id="d2e1089">The ambient hazardous trace metals exhibited distinct spatial variations across regions during this period. Nearly all trace metal concentrations in India (Ind), WE, and NA showed significant decreases following the COVID-19 outbreak (Figs. <xref ref-type="fig" rid="F3"/> and S5). For example, particulate As concentrations in these regions decreased by 8 %, 18 %, and 11 %, respectively. These reductions are likely linked to the high trace metal emissions during the “business-as-usual” period, driven by fossil fuel combustion for industrial activities (activity level decreased by 23 %), which were substantially curtailed by stay-at-home orders (Bai et al., 2023; Doumbia et al., 2021). In China, the concentrations of As, Cu, Mn, and V decreased by 10 %, 8 %, 11 %, and 11 %, respectively. However, ambient levels of Cd, Ni, Pb, and Zn increased by 3 %, 2 %, 6 %, and 7 %, respectively. It was assumed that most of these trace metals were mainly derived from residential fossil fuel combustion (increase by 5 %) and essential industrial emissions (remained relatively stable) (Zhu et al., 2020; Zhu et al., 2018), which even increased due to the stay-at-home order. In SA, the concentrations of nearly all of the trace metals showed slight decreases during the COVID-19 period. Conversely, ambient trace metal concentrations in SS and Australia (Aus) were relatively insensitive to COVID-19 lockdown measures, remaining stable or showing slight increases throughout the period. It was supposed that the concentrations of trace metals in these regions were relatively low during the “business-as-usual” period. Besides, the natural source dominated the ambient trace metal concentrations in Australia, which remained relatively stable or slight increases during COVID-19 period.</p>

      <fig id="F4" specific-use="star"><label>Figure 4</label><caption><p id="d2e1097">The emission and meteorological contributions to ambient As concentrations during 2017–2020 at global and eight major regions. Chi, Ind, WE, NA, SA, SS, Rus, and Aus represent China, India, Western Europe, North America, South America, Sub-Sahara Africa, Russia, and Australia, respectively.</p></caption>
          <graphic xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025-f04.png"/>

        </fig>

      <p id="d2e1106">Although the absolute concentrations provide an overall indication of the impact of lockdown measures on ambient trace metals, the contribution of meteorological factors cannot be disregarded. Meteorological conditions can significantly influence ambient trace metal concentrations, potentially complicating the interpretation of trace metal responses to emission changes. To isolate this effect, we applied the isolation technique to separate the contributions of emission changes from those of meteorological factors. At the global scale, most ambient trace metal concentrations, except for Pb and Zn, showed slight decreases, reflecting minor emission reductions coupled with favorable meteorological conditions that decreased concentrations (Figs. <xref ref-type="fig" rid="F4"/> and S6–S13). However, the slight increases in Pb and Zn concentrations were likely due to the fact that favorable meteorological conditions could not offset the significant rise in emissions of these metals during the period. It is assumed that Pb and Zn were primarily derived from coal combustion and non-ferrous smelting industries (Li et al., 2023a). In our study, the global residential energy consumption even increased by 5 % during COVID-19 period based on the statistical data (<uri>https://www.iea.org/</uri> (last access: 21 May 2025), which could lead to slight increases of Pb and Zn concentrations. Previous studies also have confirmed that residential coal consumption increased notably (10 %–20 %) during the lockdown period (Li et al., 2021; Smith et al., 2021). Emission changes and meteorological conditions exhibited significant spatial heterogeneity. In China, overall meteorological conditions were not favorable to the trace metal removal (Chang et al., 2020; Huang et al., 2021; Li et al., 2023b). Our previous studies also have confirmed that the low wind speed and high relative humidity aggravated the particle pollution during COVID-19 period in China (Li et al., 2023b). Despite this, the concentrations of most trace metals still showed marked decreases due to large emission reduction. However, emission-induced concentrations of Cd, Ni, Pb, and Zn in China still showed slight increases during the COVID-19 period, suggesting that essential sectors, such as coal and non-ferrous industries, could not be fully shut down. The data of National Bureau of Statistics (<uri>https://data.stats.gov.cn/index.htm</uri>, last access: 30 April 2025) also verified that the coal consumption and products of non-ferrous industries in China nearly remained invariable during this period. In regions like India, WE, and NA, favorable meteorological conditions combined with substantial emission reductions led to decreases in most trace metal concentrations. Keller et al. (2021) demonstrated that stay-at-home orders in WE and parts of NA resulted in more than a 50 % reduction in <inline-formula><mml:math id="M45" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">NO</mml:mi><mml:mi>x</mml:mi></mml:msub></mml:mrow></mml:math></inline-formula> emissions (mainly from vehicle emission and industrial activity), a trend consistent with the trace metal reductions observed in our study. Furthermore, our results suggested that the natural-derived trace metal concentrations in WE showed marked decreases (e.g., Cr (<inline-formula><mml:math id="M46" display="inline"><mml:mo lspace="0mm">-</mml:mo></mml:math></inline-formula>16 %), Cu (<inline-formula><mml:math id="M47" display="inline"><mml:mo lspace="0mm">-</mml:mo></mml:math></inline-formula>18 %), and Mn (<inline-formula><mml:math id="M48" display="inline"><mml:mo lspace="0mm">-</mml:mo></mml:math></inline-formula>18 %) during COVID-19 period, which also promoted the decreases of the trace metal concentrations in WE (Figs. S14–S22). In SA, the emission-induced reductions of trace metals were more pronounced than those due to meteorological conditions. This might be because countries such as Chile and Brazil have relatively high non-essential trace metal emissions, which were strongly affected by lockdown measures (Huber et al., 2016; La Colla et al., 2021; Zhu et al., 2020). In SS, the lockdown measures did not show marked impact on trace metal concentrations and their concentrations even experienced slight increases due to high dust contribution. In Australia, emission-induced reductions (even display slight increase) were also less significant compared to China, WE, and NA. Despite its developed mineral mining industries, Australia has more effective pollution control measures, resulting in lower total trace metal emissions (Zhu et al., 2020; Pacyna and Pacyna, 2001; Zhou et al., 2015). Moreover, most of the ambient trace metals in Australia were mainly sourced from the natural emissions (e.g., dust emissions), which was closely associated with the local meteorological conditions (Fig. S14–S22).</p>
      <p id="d2e1151">In order to assess the response of trace metal concentrations to assumed emission change, the five emission scenarios (base (annual average concentration in 2019), 20 %, 40 %, 60 %, and 80 %) were set up to evaluate the impact of emission reduction. In our study, the results suggested that the As concentrations in China, India, WE, NA, SA, SS, Russia, and Australia decreased from 1.14, 0.55, 0.13, 0.09, 0.04, 0.01, 0.08, and 0.01 to 0.23, 0.11, 0.03, 0.02, 0.01, 0, 0.02, and 0 <inline-formula><mml:math id="M49" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ng</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula> (Fig. S13a), respectively. Besides, concentrations of other trace metals also displayed linear decreases with the increasing of emission reduction ratio (Fig. S23). It was assumed that these trace metals did not participate in chemical reactions in the atmosphere and were only affected by physical processes.</p>
</sec>
<sec id="Ch1.S3.SS3">
  <label>3.3</label><title>Unexpected health benefits from COVID-19 period</title>
      <p id="d2e1176">Based on the Eqs. (<xref ref-type="disp-formula" rid="Ch1.E3"/>)–(<xref ref-type="disp-formula" rid="Ch1.E5"/>), the global health risk indicators including CR (carcinogenic risk) and HQ (hazard quotient) values were calculated. At the global scale, among all of the trace metals, Pb showed the highest CR values (9.8 <inline-formula><mml:math id="M50" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (adult, 95 % CI: 7.4 <inline-formula><mml:math id="M52" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–1.2 <inline-formula><mml:math id="M54" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M55" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">7</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula> and 2.4 <inline-formula><mml:math id="M56" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−7</sup> (children, 95 % CI: 1.8 <inline-formula><mml:math id="M58" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−7</sup>–3 <inline-formula><mml:math id="M60" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−7</sup>)), followed by Ni (3.6 <inline-formula><mml:math id="M62" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 2.8 <inline-formula><mml:math id="M64" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–4.4 <inline-formula><mml:math id="M66" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>)  and 8.7 <inline-formula><mml:math id="M68" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 6.7 <inline-formula><mml:math id="M70" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–1.1 <inline-formula><mml:math id="M72" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M73" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">7</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>), Cd (3.4 <inline-formula><mml:math id="M74" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 2.7 <inline-formula><mml:math id="M76" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–4.1 <inline-formula><mml:math id="M78" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>) and 8.4 <inline-formula><mml:math id="M80" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 6.7 <inline-formula><mml:math id="M82" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–1 <inline-formula><mml:math id="M84" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M85" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">7</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>), As (1.7 <inline-formula><mml:math id="M86" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 1.4 <inline-formula><mml:math id="M88" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–2 <inline-formula><mml:math id="M90" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>) and 4.1 <inline-formula><mml:math id="M92" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 3.3 <inline-formula><mml:math id="M94" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–4.9 <inline-formula><mml:math id="M96" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M97" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">8</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>), and Cr (1.5 <inline-formula><mml:math id="M98" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 1.2 <inline-formula><mml:math id="M100" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–1.8 <inline-formula><mml:math id="M102" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>) and 3.6 <inline-formula><mml:math id="M104" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup> (95 % CI: 2.8 <inline-formula><mml:math id="M106" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−8</sup>–4.4 <inline-formula><mml:math id="M108" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M109" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">8</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>), and the lowest ones for Cu, Mn, V, and Zn for both of adults and children, respectively. For non-carcinogenic risk, HQ values showed the higher values for As (3.7 <inline-formula><mml:math id="M110" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup> (95 % CI: 2.6 <inline-formula><mml:math id="M112" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup>–4.8 <inline-formula><mml:math id="M114" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup>) and 9.1 <inline-formula><mml:math id="M116" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup> (95 % CI: 6.6 <inline-formula><mml:math id="M118" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup>–1.2 <inline-formula><mml:math id="M120" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M121" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">4</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>) and Cu (2.4 <inline-formula><mml:math id="M122" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup> (95 % CI: 1.7 <inline-formula><mml:math id="M124" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup>–3.1 <inline-formula><mml:math id="M126" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup>) and 5.7 <inline-formula><mml:math id="M128" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup> (95 % CI: 4.1 <inline-formula><mml:math id="M130" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<sup>−5</sup>–7.3 <inline-formula><mml:math id="M132" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 10<inline-formula><mml:math id="M133" display="inline"><mml:mrow><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">5</mml:mn></mml:mrow></mml:msup><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula>). The results were in good agreement with previous studies because As often showed the higher non-carcinogenic risk (Li et al., 2023c).</p>

      <fig id="F5" specific-use="star"><label>Figure 5</label><caption><p id="d2e2018">The total CR and HQ differences of adults and children for all of the nine hazardous trace metals during January–April during 2017–2019 and 2020 (the minus of CR and HQ values in 2020 and those during 2017–2019).</p></caption>
          <graphic xlink:href="https://acp.copernicus.org/articles/25/13007/2025/acp-25-13007-2025-f05.png"/>

        </fig>

      <p id="d2e2027">The CR and HQ values can be summed to estimate the total carcinogenic and non-carcinogenic risks. By comparing the CR and HQ values between 2017–2019 and 2020, we quantified the health burden (or benefits) attributable to the COVID-19 lockdown (Figs. <xref ref-type="fig" rid="F5"/>, S24 and S25). At the spatial scale, significant decreases in health burden were observed across most regions of the NCP, Southeast China, WE, the Dun River Basin, and the eastern United States. Following 23 January 2020, at least 29 provinces in China reported confirmed COVID-19 cases. In response, strict control measures, including the shutdown of commercial activities and the lockdown of entire cities, were implemented. These measures significantly reduced emissions, particularly in populous regions such as the NCP and Southeast China (Jia et al., 2021; Shi and Brasseur, 2020). Similarly, in New York, stay-at-home orders and social restrictions were rigorously enforced by late March 2020 (Tzortziou et al., 2022). These interventions contributed to substantial reductions in trace metal emissions, thereby mitigating associated health damages. In contrast, notable increases in health burden were observed in Northeast China, the southern coastal regions of China, and certain scattered areas in the Middle East. The rise in health risks linked to trace metal exposure in Northeast China and southern coastal regions may be associated with pollution aggravation during the COVID-19 period (Huang et al., 2021). This is primarily because these regions have relatively high humidity, which facilitates the aggregation of fine particulate matter. Additionally, low wind speeds and limited environmental capacity hinder the dispersion of pollutants, leading to elevated concentrations of particulate matter and high levels of trace metals adsorbed onto these particles (Huang et al., 2021; Li et al., 2023b). Previous studies have highlighted that these regions experienced persistent air pollution or increased metal concentrations during the lockdown, primarily due to unfavorable meteorological conditions (Li et al., 2023b). For instance, the prevalence of stable weather patterns, such as reduced wind speeds and atmospheric stagnation, significantly elevated ambient trace metal concentrations (McClymont and Hu, 2021; Şahin, 2020). To confirm the assumption, we isolated the contributions of emission change and meteorology to the total changes of health risks. For instance, the emission-induced CR and HQ values of As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn accounted for <inline-formula><mml:math id="M134" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>111 %, 95 %, <inline-formula><mml:math id="M135" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>121 %, <inline-formula><mml:math id="M136" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>113 %, <inline-formula><mml:math id="M137" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>112 %, 129 %, 60 %, <inline-formula><mml:math id="M138" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>111 %, and 101 % of the total changes after COVID-19 outbreak, respectively. The meteorology-induced CR and HQ values of As, Cd, Cr, Cu, Mn, Ni, Pb, V, and Zn accounted for 11 %, 5 %, 21 %, 13 %, 12 %, <inline-formula><mml:math id="M139" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>29 %, 40 %, 11 %, and <inline-formula><mml:math id="M140" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1 %, respectively. The results were in good agreement with our assumptions, indicating Chinese lockdown measures overcome the unfavorable meteorological conditions to decrease the health risks associated with the trace metal exposures (Table S17).</p>
      <p id="d2e2083">During the COVID-19 period, China and India demonstrated the highest health benefits resulting from reductions in trace metal emissions. Additionally, WE, NA, and Russia also exhibited significant health benefits. In contrast, SS and Australia showed the lowest health benefits, with some areas even experiencing an increase in health burden following the COVID-19 outbreak. The ambient trace metals in SS and Australia appeared to be less sensitive to lockdown measures due to relatively low baseline trace metal exposures in these regions. Combined the response of trace metal concentration to emission reduction in five scenarios, we also demonstrated that trace metal emission reductions are most effective in mitigating health damages in regions with high baseline exposures, such as China and India. Future efforts to target emission reductions in these regions could yield substantial public health benefits.</p>
      <p id="d2e2086">In addition, we performed the sensitivity experiment to assess the responses of CR and HQ values to some indicators. The results suggested that both of InhR and BW showed the approximately linear relationship with both of CR and HQ values (Fig. S26). Overall, the results confirmed the health risk assessment model was robust because both of CR and HQ values did not show intense or irregular changes along with the linear change of InhR and BW.</p>
</sec>
</sec>
<sec id="Ch1.S4" sec-type="conclusions">
  <label>4</label><title>Conclusions and implications</title>
      <p id="d2e2098">The global lockdowns during the COVID-19 pandemic significantly reduced anthropogenic emissions, yet the response of ambient trace metal concentrations to these control measures remains insufficiently understood. In this study, we developed an updated global trace metal emission inventory and employed a chemical transport model to predict the concentrations of nine trace metals for January–April in 2017–2019 and 2020. Our results revealed that the response characteristics of trace metals to lockdown measures varied substantially. Global average concentrations of ambient As, Cd, Cr, Cu, Mn, Ni, and V decreased by 8 %, 1 %, 4 %, 7 %, 9 %, 6 %, and 10 %, respectively, following the COVID-19 outbreak. However, global average concentrations of particulate Pb (0.4 %) and Zn (2 %) showed slight increases during the same period. This trend can be attributed to coal combustion and non-ferrous smelting industries for essential sectors, which are critical sectors for meeting residential needs and thus less responsive to emission control measures. Significant spatial variations in trace metal responses to lockdown measures were also observed. For instance, lockdown interventions were more effective in reducing trace metal pollution in India, WE, and NA compared to other regions. Moreover, the trace metal concentrations show the linear response to emission reduction, and thus the prioritizing emission reductions in heavily polluted areas (e.g., China, India, WE, and NA) yields higher marginal benefits and greater public health gains. From a health burden perspective, controlling emissions of Pb and As emerged as the most effective strategies for mitigating carcinogenic and non-carcinogenic risks, respectively. Both elements are primarily associated with fossil fuel combustion (coal combustion). However, the persistent increase in energy consumption poses a challenge to achieving meaningful reductions in Pb and As emissions. In the future, it will be essential to implement additional control measures to curb Pb and As emissions during coal combustion processes, thereby maximizing health benefits and reducing environmental risks.</p>
      <p id="d2e2101">It is important to acknowledge several limitations in our study. Firstly, the simulated concentrations of hazardous trace metals in SA and SS might contain uncertainties due to the scarcity of ground-level observations in these regions. This lack of observational data makes it challenging to accurately evaluate the predictive reliability of ambient trace metal concentrations in these areas. Consequently, these uncertainties may also propagate to the health risk assessments. To address this, it is crucial to establish more monitoring sites for ambient trace metals in SA and SS. Secondly, the health risk assessment in this study was based solely on trace metal concentrations, without considering population exposure. In reality, health impacts are closely tied to population size and distribution. Future research should prioritize the development of more accurate methodologies that incorporate population exposure to better assess the health impacts of ambient trace metal exposure.</p>
</sec>

      
      </body>
    <back><notes notes-type="codeavailability"><title>Code availability</title>

      <p id="d2e2109">The GEOS-Chem model is available at <uri>https://geoschem.github.io/</uri> (last access: 6 October 2025).</p>
  </notes><notes notes-type="dataavailability"><title>Data availability</title>

      <p id="d2e2118">The meteorological data including MERRA-2 are available at <uri>http://geoschemdata.wustl.edu/ExtData/</uri> (last access: 6 October 2025).</p>
  </notes><app-group>
        <supplementary-material position="anchor"><p id="d2e2124">The supplement related to this article is available online at <inline-supplementary-material xlink:href="https://doi.org/10.5194/acp-25-13007-2025-supplement" xlink:title="pdf">https://doi.org/10.5194/acp-25-13007-2025-supplement</inline-supplementary-material>.</p></supplementary-material>
        </app-group><notes notes-type="authorcontribution"><title>Author contributions</title>

      <p id="d2e2133">Conceptualization: RL, Data Curation: WS and XL, Formal analysis: RL.</p>
  </notes><notes notes-type="competinginterests"><title>Competing interests</title>

      <p id="d2e2139">The contact author has declared that none of the authors has any competing interests.</p>
  </notes><notes notes-type="disclaimer"><title>Disclaimer</title>

      <p id="d2e2145">Publisher's note: Copernicus Publications remains neutral with regard to jurisdictional claims made in the text, published maps, institutional affiliations, or any other geographical representation in this paper. While Copernicus Publications makes every effort to include appropriate place names, the final responsibility lies with the authors. Also, please note that this paper has not received English language copy-editing. Views expressed in the text are those of the authors and do not necessarily reflect the views of the publisher.</p>
  </notes><ack><title>Acknowledgements</title><p id="d2e2151">This work was supported by the National Natural Science Foundation of China (42577111); Opening Project of Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention (LAP3) (grant number FDLAP24002); Academic Mentorship for Scientific Research Cadre Project (grant number AMSCP-24-05-03).</p></ack><notes notes-type="financialsupport"><title>Financial support</title>

      <p id="d2e2156">This research has been supported by the National Natural Science Foundation of China (grant no. U23A2030).</p>
  </notes><notes notes-type="reviewstatement"><title>Review statement</title>

      <p id="d2e2162">This paper was edited by Sergio Rodríguez and reviewed by two anonymous referees.</p>
  </notes><ref-list>
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