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Explaining trends and changing seasonal cycles of surface ozone in North America and Europe over the 2000-2018 period: a global modelling study with NOx and VOC tagging

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F25%3A10508719" target="_blank" >RIV/00216208:11320/25:10508719 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=yLS.MEe6RQ" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=yLS.MEe6RQ</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.5194/acp-25-16833-2025" target="_blank" >10.5194/acp-25-16833-2025</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Explaining trends and changing seasonal cycles of surface ozone in North America and Europe over the 2000-2018 period: a global modelling study with NOx and VOC tagging

  • Original language description

    Surface ozone, with its long enough lifetime, can travel far from its precursor emissions, affecting human health, vegetation, and ecosystems on an intercontinental scale. Recent decades have seen significant shifts in ozone precursor emissions: reductions in North America and Europe, increases in Asia, and a steady global rise in methane. Observations from North America and Europe show declining ozone trends, a flattened seasonal cycle, a shift in peak ozone from summer to spring, and increasing wintertime levels. To explain these changes, we use TOAST 1.0, a novel ozone tagging technique implemented in the global atmospheric model CAM4-Chem which attributes ozone to its precursor emissions fully by NOx or VOC+CO+CH4 sources and perform multi-decadal model simulations for 2000-2018. Model-simulated maximum daily 8 h ozone (MDA8 O3) agrees well with rural observations from the TOAR-II database. Our analysis reveals that declining local NOx contributions to peak-season ozone (PSO) in North America and Europe are offset by rising contributions from natural NOx (due to increased O3 production), and foreign anthropogenic- and international shipping NOx due to increased emissions. Transported ozone dominates during spring. Methane is the largest VOC contributor to PSO, while natural NMVOCs become more important in summer. Contributions from anthropogenic NMVOCs remain smaller than those from anthropogenic NOx. Despite rising global methane levels, its contribution to PSO in North America and Europe has declined due to reductions in local NOx emissions. Our results highlight the evolving drivers of surface ozone and emphasize the need for coordinated global strategies that consider both regional emission trends and long-range pollutant transport.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10509 - Meteorology and atmospheric sciences

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Atmospheric Chemistry and Physics

  • ISSN

    1680-7316

  • e-ISSN

    1680-7324

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    22

  • Country of publishing house

    DE - GERMANY

  • Number of pages

    44

  • Pages from-to

    16833-16876

  • UT code for WoS article

    001622705900001

  • EID of the result in the Scopus database

    2-s2.0-105023319728