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Control of toxicity of fine particulate matter emissions in China

Abstract

Fine particulate matter (particulate matter with a diameter of 2.5 μm or less; PM2.5) causes millions of premature deaths globally1, but not all particles are equally harmful2,3,4. Current air-pollution control strategies, prioritizing PM2.5 mass reduction, have provided considerable health benefits but further refinements based on differences in the toxicity of various emission sources may provide greater benefits5,6,7. Here we integrated field measurements with air-quality modelling to assess the unequal toxicities of PM2.5 from various anthropogenic sources. Our findings revealed that the toxicity per unit of PM2.5 mass differed substantially between major sources, differing by up to two orders of magnitude. PM2.5 from solid fuel combustion in residential stoves had the highest toxicity, followed by those from the metallurgy industry, brake wear, diesel vehicles, petrol vehicles, the cement industry and power plants. We further analysed the source contributions of toxicity-adjusted PM2.5 emissions and population exposures in China. From 2005 to 2021, both the PM2.5 mass and relative-potency-adjusted emissions substantially decreased. Although industrial sources contributed 57.5% to the reduction in PM2.5 mass emissions, the reduction in relative potency-adjusted emissions was driven by residential combustion (approximately 80%). Clean-air policies should consider the differing toxicities of PM2.5 when formulating source-specific emission control regulations. This study proposes a cellular toxicity-based framework for PM2.5 reduction that could address the specific health risks in diverse regions, but further epidemiological studies will be required to confirm their relevance to human health outcomes and their application to public policy.

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Fig. 1: Relative toxic potencies of source-specific PM2.5.
Fig. 2: Sectoral contributions to the changes in RPAE and PM2.5 emissions in China during the period 2005–2021.
Fig. 3: Spatial distribution of RPAE and relative potency of PM2.5 emissions in China in 2021.
Fig. 4: Geographical disparities in PM2.5 exposure and associated toxicity in China in 2021.

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Data availability

The results of the cellular tests of source-specific PM2.5 samples are presented in the paper and/or the Supplementary Information. The mass fractions and relative contributions to oxidative stress toxicity of individual PAHs and metals are given in the Supplementary Data. The ABaCAS emissions inventory is available online at Figshare (https://doi.org/10.6084/m9.figshare.21777005.v1)62. The base map (approval no. GS(2019)1822) of Figs. 3 and 4 and Extended Data Figs. 5, 79 is sourced from the Standard Map Service System hosted by the Ministry of Natural Resources of China (http://bzdt.ch.mnr.gov.cn/index.html). The map is used unmodified and complies with public map regulations. Source data are provided with this paper.

Code availability

The open-source numerical models WRF (v.3.9.1, https://www.mmm.ucar.edu/models/wrf) and CMAQ (v.5.3.3, https://github.com/USEPA/CMAQ) were used for the modelling. The model codes used in this work as well as sample datasets used to test the codes are available at Figshare (https://figshare.com/s/c60433809e435a82e333)63.

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Acknowledgements

This research was supported by the National Natural Science Foundation of China (grant no. 22188102 to S. Wang, grant nos. U22A20405 and T2122006 to Q. Li, and grant no. 22406026 to D.W.), the National Key Research and Development Program (grant no. 2022YFC3702905 to S. Wang and grant no. 2022YFC3700501 to Q. Li), the New Cornerstone Science Foundation through the XPLORER PRIZE (to S. Wang), the Research Grants Council of Hong Kong (grant no. T24-508/22-N to X.D.L. and L.N.J., and grant nos. 25210420, 15213922 and C2002-22Y to L.N.J.), and the ‘GeoX’ Interdisciplinary Project of Frontiers Science Center for Critical Earth Material Cycling, Nanjing University (grant no. 20250210 to H.Z.). We thank A. Cheng, Y. Tan, L. Wang and T. Liu for supporting the collection of field samples and Y. Wu, S. Zhang and Z. Fu for contributing to the emissions inventory. A.J.C. is a consulting principal scientist at the Health Effects Institute. The views expressed here are those of the authors and do not necessarily reflect the views of the Health Effects Institute, or its sponsors.

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Authors and Affiliations

Authors

Contributions

S. Wang and Q. Li conceived and designed the experiments. D.W., Q. Li, X.C. and Y.L. performed the experiments. H.Z. and D.W. analysed the data and prepared the graphs. X.D.L., L.N.J., B.Z., S.L., Y.S., Z.D., Q.W., J.C., H.T., Q. Liu, J.J., H.K., K.H., H.H., C.C., J.Z., S. Weichenthal, J.S.J., A.J.C. and J.H. contributed materials and analysis tools. H.Z. and D.W. wrote the manuscript, and all of the authors helped to revise the manuscript.

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Correspondence to Shuxiao Wang or Qing Li.

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Extended data figures and tables

Extended Data Fig. 1 Chemical drivers of PM2.5 toxicity.

The mass fractions of key toxic components in PM2.5 emissions from residential combustion (fuel types: coal and biomass), power generation (fuel types: coal, biomass, and waste), transportation (including on-road gasoline/diesel vehicles, inland waterways, and non-exhaust emissions), and industrial sections (including iron and steel, non-ferrous metallurgy, cement, industry boilers, coking, and glass production): a, 16 US EPA priority PAHs; b, 10 selected toxic metals. The data are plotted as box-and-whiskers (the line in the box is the median, the solid squares are the mean values, the edges of the boxes are the quartile ranges (25th and 75th percentiles), and the lengths of the whiskers are within 1.5 times the interquartile range). PM2.5 from residential solid fuel combustion is rich in PAHs, while industrial emissions are rich in toxic metals. Data represent 16 PAHs (n = 268) and toxic metals (n = 275) per unit mass of PM2.5 samples. Results are derived from three independent experiments, each comprising a minimum of three technical replicates.

Extended Data Fig. 2 Industrial PM2.5 emissions and RPAE in China during 2005–2021.

a, PM2.5 emissions. b, RPAEOS. c, RPAECT. The gray and black curves denote the RPOS and RPCT of the PM2.5 emissions from industrial sources (right y-axis).

Extended Data Fig. 3 Transportation PM2.5 emissions and RPAE in China during 2005–2021.

a, PM2.5 emissions. b, RPAEOS. c, RPAECT. The gray and black curves denote the RPOS and RPCT of the PM2.5 emissions from transportation sources (right y-axis).

Extended Data Fig. 4 Source-resolved contributions to PM2.5 emissions and RPAE in China during 2005–2021.

a, PM2.5 mass. b, RPAEOS. c, RPAECT. The data in parentheses are the range (minimum to maximum) of percentage contributions among provinces. Residential combustion sources dominated the reductions in RPAE while industrial sources dominated the reductions in PM2.5 mass.

Extended Data Fig. 5 Spatial distribution of PM2.5 emissions, RPAE, and RP of PM2.5 emissions in China in 2021.

a, PM2.5 emissions (resolution: 9 km × 9 km). b, RPAECT. c, RPCT of PM2.5. The bold boundaries denote the Beijing-Tianjin-Hebei (BTH) region, Yangtze River Delta (YRD), Pearl River Delta (PRD), and Northwestern China (Northwest). The base map is from the Standard Map Service System hosted by the Ministry of Natural Resources of China.

Extended Data Fig. 6 Joint probability density distributions of PM2.5 emission intensity (t/km²) versus associated relative potencies.

a, RPOS. b, RPCT. For each region, 2,000 data points were sampled from grid cells, and the joint probability densities were estimated using Seaborn’s kdeplot function in Python. The contours represent the iso-proportion levels of the data density, with the lowest level threshold set at 0.33 to highlight primary density hotspots.

Extended Data Fig. 7 Spatial distribution of the RPAE and RP of PM2.5 emissions in the Beijing-Tianjin-Hebei (BTH) region in China in 2021.

a, RPAEOS (resolution: 9 km × 9 km). b, RPOS. c, RPAECT. d, RPCT. The base map is from the Standard Map Service System hosted by the Ministry of Natural Resources of China.

Extended Data Fig. 8 Multiscale exposure-toxicity relationship for PM2.5 exposure in China in 2021.

a-c, Grid-level distributions of the PM2.5 exposure, RPOS, and RPCT of exposure. d-f, Province-level spatial distributions of the PM2.5 exposure, RPOS, and RPCT of exposure. g-h, Province-level spatial distribution of RPOS- and RPCT-adjusted exposure. The base map is from the Standard Map Service System hosted by the Ministry of Natural Resources of China.

Extended Data Fig. 9 Provincial source apportionment of PM2.5 exposure (outer ring) and RPOS- (middle ring) and RPCT-adjusted exposure (inner ring) in China in 2021.

The top three sources per category are colored distinctly, while the remaining contributors are combined as “Others” in gray. The base map is from the Standard Map Service System hosted by the Ministry of Natural Resources of China.

Supplementary information

Supplementary Information (download PDF )

Supplementary Notes 1–5 and additional references, Figs. 1–12 and Tables 1–5.

Supplementary Data (download XLSX )

The mass fractions and relative contributions to oxidative stress toxicity of individual PAHs and metals.

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Zheng, H., Wu, D., Wang, S. et al. Control of toxicity of fine particulate matter emissions in China. Nature 643, 404–411 (2025). https://doi.org/10.1038/s41586-025-09158-w

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