Changes In Ozone Precursor Emissions Research Articles

Quantifying the tropospheric ozone radiative effect and its temporal evolution in the satellite era

Abstract. Using state-of-the-art satellite ozone profile products, and a chemical transport model, we provide an updated estimate of the tropospheric ozone radiative effect (TO3RE) and observational constraint on its variability over the decade 2008–2017. Previous studies have shown the short-term (i.e. a few years) globally weighted average TO3RE to be 1.17 ± 0.03 W m−2. However, from our analysis, using decadal (2008–2017) ozone profile datasets from the Infrared Atmospheric Sounding Interferometer, average TO3RE ranges between 1.21 and 1.26 W m−2. Over this decade, the modelled and observational TO3RE linear trends show a negligible change (e.g. ± 0.1 % yr−1). Two model sensitivity experiments fixing emissions and meteorology to 1 year (i.e. start year – 2008) show that temporal changes in ozone precursor emissions (increasing contribution) and meteorological factors (decreasing contribution) have counteracting tendencies, leading to a negligible globally weighted average TO3RE trend.

Trend analysis of measured surface ozone at the megacity of Tehran for the summertime 2007–2021

High concentrations of surface ozone in urban and industrial regions worldwide have been a major air quality issue. Tehran, as the capital and the most populous city of Iran, has experienced intense ambient air pollution over the last three decades. This study aims to assess the long-term trends of ozone over this city in recent decades. Data series of maximum 8-h daily average (MDA8) ozone were obtained for the period between 2007 and 2021. To determine the MDA8 ozone trend attributed to the long-term changes in ozone precursor emissions, we isolated the effects of meteorology and short-term ozone variability. The results show a downward trend from 2007 to 2014 (P1) and an upward trend from 2014 onward (P2). The long-term precursor emissions changes contribute to a 29.1% negative trend (=−0.7 ppb year−1) over P1 and an 8.95% upward trend (=0.1 ppb year−1) over P2. To find the causes of the trend transition, we investigated the relationship between the adjusted MDA8 and several ozone precursors, namely NOx and CO. It is found that, over P1, the dominant chemistry regime is mixed, in which the decline of CO and NOx (attributed to industrial sources) is associated with the downward trend of ozone. On the other hand, the upward trend of ozone over P2 is associated with an increase in NOx mostly attributed to road transport (passenger cars) and residential sectors.

Lower air pollution during COVID-19 lock-down: improving models and methods estimating ozone impacts on crops.

We suggest that the unprecedented and unintended decrease of emissions of air pollutants during the COVID-19 lock-down in 2020 could lead to declining seasonal ozone concentrations and positive impacts on crop yields. An initial assessment of the potential effects of COVID-19 emission reductions was made using a set of six scenarios that variously assumed annual European and global emission reductions of 30% and 50% for the energy, industry, road transport and international shipping sectors, and 80% for the aviation sector. The greatest ozone reductions during the growing season reached up to 12 ppb over crop growing regions in Asia and up to 6 ppb in North America and Europe for the 50% global reduction scenario. In Europe, ozone responses are more sensitive to emission declines in other continents, international shipping and aviation than to emissions changes within Europe. We demonstrate that for wheat the overall magnitude of ozone precursor emission changes could lead to yield improvements between 2% and 8%. The expected magnitude of ozone precursor emission reductions during the Northern Hemisphere growing season in 2020 presents an opportunity to test and improve crop models and experimentally based exposure response relationships of ozone impacts on crops, under real-world conditions.This article is part of a discussion meeting issue ‘Air quality, past present and future’.

Multi-decadal surface ozone trends at globally distributed remote locations

Extracting globally representative trend information from lower tropospheric ozone observations is extremely difficult due to the highly variable distribution and interannual variability of ozone, and the ongoing shift of ozone precursor emissions from high latitudes to low latitudes. Here we report surface ozone trends at 27 globally distributed remote locations (20 in the Northern Hemisphere, 7 in the Southern Hemisphere), focusing on continuous time series that extend from the present back to at least 1995. While these sites are only representative of less than 25% of the global surface area, this analysis provides a range of regional long-term ozone trends for the evaluation of global chemistry-climate models. Trends are based on monthly mean ozone anomalies, and all sites have at least 20 years of data, which improves the likelihood that a robust trend value is due to changes in ozone precursor emissions and/or forced climate change rather than naturally occurring climate variability. Since 1995, the Northern Hemisphere sites are nearly evenly split between positive and negative ozone trends, while 5 of 7 Southern Hemisphere sites have positive trends. Positive trends are in the range of 0.5–2 ppbv decade–1, with ozone increasing at Mauna Loa by roughly 50% since the late 1950s. Two high elevation Alpine sites, discussed by previous assessments, exhibit decreasing ozone trends in contrast to the positive trend observed by IAGOS commercial aircraft in the European lower free-troposphere. The Alpine sites frequently sample polluted European boundary layer air, especially in summer, and can only be representative of lower free tropospheric ozone if the data are carefully filtered to avoid boundary layer air. The highly variable ozone trends at these 27 surface sites are not necessarily indicative of free tropospheric trends, which have been overwhelmingly positive since the mid-1990s, as shown by recent studies of ozonesonde and aircraft observations.

Detection of trends in surface ozone in the presence of climate variability

AbstractTrends in trace atmospheric constituents can be driven not also by trends in their (precursor) emissions but also by trends in meteorology. Here we use ground‐level ozone as an example to highlight the extent to which unforced, low‐frequency climate variability can drive multidecadal trends. Using output from six experiments of the Geophysical Fluid Dynamics Laboratory chemistry‐climate model (CM3), we demonstrate that 20 year trends in surface ozone driven by climate variability alone can be as large as those forced by changes in ozone precursor emissions or by anthropogenic climate change. We highlight regions and seasons where surface ozone is strongly influenced by climate variability and thus where a given forced trend may be more difficult to detect. A corollary is that this approach identifies regions and seasons of low variability, where measurement sites may be most effectively deployed to detect a particular trend driven by changing precursor emissions. We find that the representative concentration pathways 4.5 (RCP4.5) and RCP8.5 forced surface ozone trends in most locations emerge over background variability during the first half of the 21st century. Ozone trends are found to respond mostly to changes in emissions of ozone precursors and unforced climate variability, with a comparatively small impact from anthropogenic climate change. Thus, attempts to attribute observed trends to regional emissions changes require consideration of internal climate variability, particularly for short record lengths and small forced trends.

Drivers of the tropospheric ozone budget throughout the 21st century under the medium-high climate scenario RCP 6.0

Abstract. Because tropospheric ozone is both a greenhouse gas and harmful air pollutant, it is important to understand how anthropogenic activities may influence its abundance and distribution through the 21st century. Here, we present model simulations performed with the chemistry–climate model SOCOL, in which spatially disaggregated chemistry and transport tracers have been implemented in order to better understand the distribution and projected changes in tropospheric ozone. We examine the influences of ozone precursor emissions (nitrogen oxides (NOx), carbon monoxide (CO) and volatile organic compounds (VOCs)), climate change (including methane effects) and stratospheric ozone recovery on the tropospheric ozone budget, in a simulation following the climate scenario Representative Concentration Pathway (RCP) 6.0 (a medium-high, and reasonably realistic climate scenario). Changes in ozone precursor emissions have the largest effect, leading to a global-mean increase in tropospheric ozone which maximizes in the early 21st century at 23% compared to 1960. The increase is most pronounced at northern midlatitudes, due to regional emission patterns: between 1990 and 2060, northern midlatitude tropospheric ozone remains at constantly large abundances: 31% larger than in 1960. Over this 70-year period, attempts to reduce emissions in Europe and North America do not have an effect on zonally averaged northern midlatitude ozone because of increasing emissions from Asia, together with the long lifetime of ozone in the troposphere. A simulation with fixed anthropogenic ozone precursor emissions of NOx, CO and non-methane VOCs at 1960 conditions shows a 6% increase in global-mean tropospheric ozone by the end of the 21st century, with an 11 % increase at northern midlatitudes. This increase maximizes in the 2080s and is mostly caused by methane, which maximizes in the 2080s following RCP 6.0, and plays an important role in controlling ozone directly, and indirectly through its influence on other VOCs and CO. Enhanced flux of ozone from the stratosphere to the troposphere as well as climate change-induced enhancements in lightning NOx emissions also increase the tropospheric ozone burden, although their impacts are relatively small. Overall, the results show that under this climate scenario, ozone in the future is governed largely by changes in methane and NOx; methane induces an increase in tropospheric ozone that is approximately one-third of that caused by NOx. Climate impacts on ozone through changes in tropospheric temperature, humidity and lightning NOx remain secondary compared with emission strategies relating to anthropogenic emissions of NOx, such as fossil fuel burning. Therefore, emission policies globally have a critical role to play in determining tropospheric ozone evolution through the 21st century.

Declining ozone exposure of European vegetation under climate change and reduced precursor emissions

Abstract. The impacts of changes in ozone precursor emissions as well as climate change on the future ozone exposure of the vegetation in Europe were investigated. The ozone exposure is expressed as AOT40 (Accumulated exposure Over a Threshold of 40 ppb O3) as well as PODY (Phytotoxic Ozone Dose above a threshold Y). A new method is suggested to express how the length of the period during the year when coniferous and evergreen trees are sensitive to ozone might be affected by climate change. Ozone precursor emission changes from the RCP4.5 scenario were combined with climate simulations based on the IPCC SRES A1B scenario and used as input to the Eulerian Chemistry Transport Model MATCH from which projections of ozone concentrations were derived. The ozone exposure of vegetation over Europe expressed as AOT40 was projected to be substantially reduced between the periods 1990–2009 and 2040–2059 to levels which are well below critical levels used for vegetation in the EU directive 2008/50/EC as well as for crops and forests used in the LRTAP convention, despite that the future climate resulted in prolonged yearly ozone sensitive periods. The reduction in AOT40 was mainly driven by the emission reductions, not changes in the climate. For the toxicologically more relevant POD1 index the projected reductions were smaller, but still significant. The values for POD1 for the time period 2040–2059 were not projected to decrease to levels which are below critical levels for forest trees, represented by Norway spruce. This study shows that substantial reductions of ozone precursor emissions have the potential to strongly reduce the future risk for ozone effects on the European vegetation, even if concurrent climate change promotes ozone formation.

European summer surface ozone 1990–2100

Abstract. The impact of climate change and changes in ozone precursor emission on summer surface ozone in Europe was studied using a regional CTM over the period 1990 to 2100. Two different climate simulations under the SRES A1B scenario together with ozone precursor emission changes from the RCP4.5 scenario were used as model input. In southern Europe regional climate change leads to increasing surface ozone concentrations during April–September, but projected emission reductions in Europe have a stronger effect, resulting in net reductions of surface ozone concentrations. In northern Europe regional climate change decreases surface O3 and reduced European emissions acts to further strengthen this trend also when including increasing hemispheric background concentrations. The European O3 precursor emission reductions in RCP4.5 are substantial and it remains to be seen if these reductions can be achieved. There is substantial decadal variability in the simulations forced by climate variability which is important to consider when looking at changes in surface O3 concentrations, especially until the first half of the 21st century. In order to account for changes in background O3 future regional model studies should couple global (hemispheric) and regional CTMs forced by a consistent set of meteorological and precursor emission data.

Effect of regional precursor emission controls on long-range ozone transport – Part 2: Steady-state changes in ozone air quality and impacts on human mortality

Abstract. Large-scale changes in ozone precursor emissions affect ozone directly in the short term, and also affect methane, which in turn causes long-term changes in ozone that affect surface ozone air quality. Here we assess the effects of changes in ozone precursor emissions on the long-term change in surface ozone via methane, as a function of the emission region, by modeling 10% reductions in anthropogenic nitrogen oxide (NOx) emissions from each of nine world regions. Reductions in NOx emissions from all world regions increase methane and long-term surface ozone. While this long-term increase is small compared to the intra-regional short-term ozone decrease, it is comparable to or larger than the short-term inter-continental ozone decrease for some source-receptor pairs. The increase in methane and long-term surface ozone per ton of NOx reduced is greatest in tropical and Southern Hemisphere regions, exceeding that from temperate Northern Hemisphere regions by roughly a factor of ten. We also assess changes in premature ozone-related human mortality associated with regional precursor reductions and long-range transport, showing that for 10% regional NOx reductions, the strongest inter-regional influence is for emissions from Europe affecting mortalities in Africa. Reductions of NOx in North America, Europe, the Former Soviet Union, and Australia are shown to reduce more mortalities outside of the source regions than within. Among world regions, NOx reductions in India cause the greatest number of avoided mortalities per ton, mainly in India itself. Finally, by increasing global methane, NOx reductions in one hemisphere tend to cause long-term increases in ozone concentration and mortalities in the opposite hemisphere. Reducing emissions of methane, and to a lesser extent carbon monoxide and non-methane volatile organic compounds, alongside NOx reductions would avoid this disbenefit.

Ozone air quality and radiative forcing consequences of changes in ozone precursor emissions

[1] Changes in emissions of ozone (O3) precursors affect both air quality and climate. We first examine the sensitivity of surface O3 concentrations (O3srf) and net radiative forcing of climate (RFnet) to reductions in emissions of four precursors – nitrogen oxides (NOx), non-methane volatile organic compounds, carbon monoxide, and methane (CH4). We show that long-term CH4-induced changes in O3, known to be important for climate, are also relevant for air quality; for example, NOx reductions increase CH4, causing a long-term O3 increase that partially counteracts the direct O3 decrease. Second, we assess the radiative forcing resulting from actions to improve O3 air quality by calculating the ratio of ΔRFnet to changes in metrics of O3srf. Decreases in CH4 emissions cause the greatest RFnet decrease per unit reduction in O3srf, while NOx reductions increase RFnet. Of the available means to improve O3 air quality, therefore, CH4 abatement best reduces climate forcing.

Ozone air quality and radiative forcing consequences of changes in ozone precursor emissions

Ozone air quality and radiative forcing consequences of changes in ozone precursor emissions