Of the greenhouse gases (CO2, CH4, O3, N2O, H2O, synthetic greenhouse gases, e.g. HFCs, SF6) tropospheric ozone is perhaps the most difficult to observe and quantify on the global scale, due to its acute spatial variability resulting from its variable lifetime (minutes in the polluted boundary layer, to roughly three weeks in the free troposphere [Young et al., 2013]) and its range of sources (injection from the stratosphere, or photochemical production from natural and anthropogenic precursor gases) and sinks (surface deposition and chemical destruction) [Monks et al., 2009; 2015; Lin et al., 2019]. The challenge is compounded by varying emissions of ozone precursor gases which, over the past few decades, have shifted from high and mid-latitudes toward low latitudes, where ozone production efficiency is greater [Zhang et al., 2016]. With respect to quantifying tropospheric ozone’s impact on climate change, the most useful observations are those from globally distributed, long-term surface sites in remote locations, and free tropospheric observations (ozonesonde or aircraft), especially those from the upper troposphere, where ozone’s long-wave radiative effect is most effective [Kuai et al., 2017].
Since the 1990s, periodic updates of observed surface and free tropospheric ozone trends in remote locations have appeared in the literature at irregular intervals [e.g. Logan 1985, 1999a, b, 2012; Oltmans and Levy, 1994; Oltmans et al., 1998, 2006, 2013; Parrish et al., 2012; Gaudel et al., 2018]. These data analyses have been complemented by a series of assessments that summarize the current state of knowledge regarding tropospheric ozone’s global distribution and trends [e.g. IPCC, 2013; Cooper et al., 2014; Gaudel et al., 2018; Blunden et al., 2018]. These studies and assessments have been extremely useful for keeping the research community and policy makers informed on tropospheric ozone’s trends and variability. However, due to ozone’s continuous global redistribution and the 1–2 year time lag between data availability and publication date, these findings quickly become outdated. Furthermore, most of the previous global trend analyses focused on very few sites, some of which were impacted by local and regional pollution sources, as will be shown later.
Recently, The Tropospheric Ozone Assessment Report (TOAR) produced a series of peer-reviewed publications that documented the state of knowledge on ozone’s global distribution and trends, relying on surface observations through the year 2014 (https://collections.elementascience.org/toar). While TOAR provided a wide range of analysis on global ozone trends with relevance to climate [see Gaudel et al., 2018, also known as TOAR-Climate] it could not cover every aspect in detail. Fortunately, TOAR was specifically designed to enable new research, independent of the original TOAR effort, allowing future studies to explore unaddressed science questions. This paper is part of that growing legacy, joining several new independent studies that have been enabled by the wide range of ozone metrics archived in the TOAR Surface Ozone Database [Lu et al., 2018; Jaffe et al., 2018; Strode et al., 2018; Chang et al., 2019; Shen et al., 2019; Seltzer et al., 2020]. Our analysis has several goals: 1) identify the most useful sites in the TOAR database for understanding long-term ozone trends at remote locations worldwide, for the purpose of evaluating global chemistry-climate models; 2) document and display the wide range of ozone trends and multi-year ozone fluctuations recorded at remote sites around the world using the most recently available data (most sites have data through 2017–2018); 3) demonstrate that the ozone trends recorded at high altitude Alpine sites in central Europe do not match the ozone increases observed by commercial aircraft in the lower free troposphere above Europe; and 4) use the TOAR database and the recent peer-reviewed literature to place these remote ozone time series in the context of ozone trends observed in the polluted boundary layer and the free troposphere.
This analysis focuses on ozone observations from 27 remotes sites, selected from over 9000 ozone time series in the TOAR Surface Ozone Database [Schultz et al., 2017]. Although few in number, these are the best available sites for understanding long-term ozone trends at remote locations worldwide, and they are well suited for evaluating the ozone trends calculated by the global chemistry-climate models that simulate the evolution of tropospheric ozone on multi-decadal time scales [Collins et al., 2017; Myhre et al., 2017; Young et al., 2018]. Our analysis goes beyond the scope of TOAR, which only addressed five of the 27 sites selected for this paper [Gaudel et al., 2018], by using the most recently available data, and by using a more refined trend analysis method that is based on monthly anomalies.
The analysis and results are presented as follows. Section 2 describes the site selection method and the statistical analysis applied to estimate the long-term ozone trends at each site, as well as periods of multi-year ozone fluctuations. Sites were limited to those with continuous ozone time series that extend from the present back to at least 1995, so that multi-decadal ozone trends can be assessed. Importantly, all sites have at least 20 years of data, which improves the likelihood that any robust trend value is due to changes in ozone precursor emissions and/or forced climate change rather than naturally occurring climate variability [Weatherhead et al., 1998; Barnes et al., 2016]. Section 3 presents the results of the trend analysis focusing on: 1) the four longest remote ozone time series, established in the mid-1970s; 2) all 27 remote sites since 1995; and 3) a comparison between the long-term trends at the high elevation surface sites in the Alps, and the lower free-troposphere above Europe, as observed by commercial aircraft. Section 4 provides context for the ozone trends at the 27 remote sites by comparing them to observed trends in the polluted boundary layer and the free troposphere. Finally, Appendix S-A in the Supplemental Material describes the advantages of the statistical methods employed by this study over those used by TOAR. The appendix also provides a comparison between these statistical methods and several other popular methods, as well as an evaluation of polynomial fits, which can lead to inaccurate trend estimates.
All ozone observations reported in this paper were made using the standard modern method, based on ozone’s ultraviolet (UV) absorption cross-section [Galbally et al., 2013], with the exception of some early observations made in the 1950s–1970s, as described below. A history of the UV-absorption method and its comparison to a wide range of other ozone measurement techniques is provided by the Tropospheric Ozone Assessment Report (TOAR) [Tarasick and Galbally et al., 2019]. We report ozone observations from 27 remote surface sites, listed in Table 1, along with their locations and the original data sources. Many of these sites are part of the World Meteorological Organization’s (WMO) Global Atmosphere Watch (GAW) program and therefore follow strict data quality control guidelines [Galbally et al., 2013; Schultz et al., 2015], with station audits and calibration information available from the World Calibration Centre for Surface Ozone, Carbon Monoxide, Methane and Carbon Dioxide [Klausen et al., 2003; Buchmann et al., 2009; WCC-Empa, 2019]. All surface ozone data were uploaded to the TOAR Surface Ozone Database [Schultz et al., 2017], processed by the TOAR Database team and then retrieved from the TOAR Surface Ozone Database via the JOIN web interface: https://join.fz-juelich.de. Data processing involved reformatting the data, and where necessary, unit conversions and time shift to UTC. Ozone observations made from commercial aircraft above Western Europe are also used, as described below.
lat. long. alt. (m a.s.l.)
|Years with data||Monitoring institution or network2||Primary data source|
|Remote sites in the Northern Hemisphere|
|Alert, Canada (P)
82.5° N, 62.5° W, 187 m
|Zeppelin, Svalbard (P)
78.9° N, 11.9° E, 474 m
|Barrow, Alaska (P,M)
71.3° N, 156.6° W, 11 m
|Esrange, Sweden (P)
67.9 ° N, 21.1° E, 524 m
65.8 N, 13.9° E, 439 m
63.7° N, 149.0° W, 663 m
|1987–2017||US EPA CASTNET||https://www.epa.gov/castnet|
|Strath Vaich Dam, Scotland
57.7° N, 4.8° W, 266 m
|1987–2017||Scottish Environment Protection Agency||1987–2016: http://ebas.nilu.no/
|Mace Head, Ireland (M)
53.3° N, 9.9° W, 8 m
|1988–2017||GAW/National University of Ireland Galway||http://ebas.nilu.no/|
|IAGOS profiles above northwestern Europe
47°–55° N, 0°–15° E
|Zugspitze, Germany (H,Mt)
47.4° N, 11.0° E, 2800 m
|Sonnblick, Austria (H,Mt)
47.1° N, 13.0° E, 3106 m
|Jungfraujoch, CH (H,Mt)
46.5° N, 8.0° E, 3580 m
|Kislovodsk, Russia (H,Mt)
43.7° N, 42.7° E, 2096 m
|1989–2013||Oboukhov Institute of Atmospheric Physics||Irina Senik, personal communication to TOAR|
|Centennial, Wyoming (H)
41.4° N, 106.2° W, 3175 m
|1989–2017||US EPA CASTNET||https://www.epa.gov/castnet|
|Great Basin, Nevada (H)
39.0° N, 114.2° W, 2058 m
|1993–2017||US EPA CASTNET||https://www.epa.gov/castnet|
|Gothic, Colorado (H)
39.0° N, 107° W, 2915 m
|1989–2017||US EPA CASTNET||https://www.epa.gov/castnet|
|Grand Canyon, Arizona (H)
36.1° N, 112.2° W, 2073 m
|1989–2017||US EPA CASTNET||https://www.epa.gov/castnet|
|Mt. Waliguan, China (H,Mt)
36.3° N, 100.9° E, 3810 m
|1994–2016||GAW/China Meteorological Administration||http://www.cma.gov.cn/en2014|
|Izaña, Canary Islands (H,Mt)
28.3° N, 16.5° W, 2367 m
|1987–2017||GAW/Izaña Atmospheric Research Centre, AEMET||http://ebas.nilu.no/|
|Minamitorishima, N. Pacific
24.3° N, 154° E, 8 m (M)
|1994–2018||GAW/Japan Meteorological Agency||http://ebas.nilu.no/|
|MLO, Hawaii (H,Mt,T)
19.5° N, 155.6° W, 3397 m
|Remote sites in the Southern Hemisphere|
|American Samoa, S. Pacific
–14.2° S, 170.6° W, 42 m (M,T)
|El Tololo, Chile
30.2 S, 70.8 W, 2220 m (Mt)
|1995–2016||GAW/Dirección Meteorológica de Chile||
|Cape Point, South Africa (M)
34.4° S, 18.5° E, 230 m
|1983-2017||GAW/South African Weather Service||Thumeka Mkololo, personal communication to TOAR|
|Cape Grim, Tasmania (M)
40.7° S, 144.7° E, 94 m
|1982–2017||GAW/Australian Bureau of Meteorology and CSIRO||https://www.gaw-wdcrg.org/|
54.8° S, 68.3° W, 18 m
|1994–2017||GAW/Servicio Meteorológico Nacional||http://www3.smn.gob.ar/?mod=htms&id=8|
|Neumayer, Antarctica (P)
70.7° S, 8.3° W, 42 m
|1995–2017||GAW/Alfred Wegener Institute||http://ebas.nilu.no/|
|South Pole, Antarctica (P,H)
90.0° S, 59.0° E, 2840 m
|Rural sites in the boundary layer of southern Germany|
49.3° N, 7.8° E, 606 m
|1990–2018||Landesamt für Umwelt, Wasserwirtschaft und Gewerbeaufsicht, Rheinland Pfalz||UBA Germany, personal communication|
47.8° N, 11.0° E, 985 m
47.8° N, 7.8° E, 920 m
|1990–2018||Landesamt für Umwelt, Messungen und Naturschutz, Baden-Württemberg||UBA Germany, personal communication|
To describe and quantify the long term changes in ozone at each site we chose a linear regression model (described below) to quantify the ozone rate of change, and locally weighted regression (or lowess, or loess smoother) to describe the nonlinear multi-year ozone fluctuations at each site [Cleveland, 1979; Cleveland and Devlin, 1988]. We considered other statistical methods for estimating the long-term rate of change and multiyear fluctuations, and we provide a detailed comparison of all methods in Appendix S-A to demonstrate why the linear regression model and locally weighted regression are appropriate for this study.
Due to ozone’s strong seasonal cycle, the trend estimated from monthly observed ozone can be less accurate than the trend estimated from monthly anomalies, if several months of data are missing. Therefore, we report trends based on monthly mean ozone anomalies, which also reveal the influence of unforced climate variability on interannual ozone fluctuations [Logan et al., 2012; Oltmans et al., 2013; Tarasick et al., 2016; Lin et al., 2014; 2015; 2017]. The observed monthly means are calculated by the TOAR Surface Ozone Database from hourly observations (for either daytime or nighttime conditions, as described below). Acceptance of a monthly mean depends on the hourly data availability being greater than 75%; the data availability requirement was relaxed to 50% for Kislovodsk due to intermittent data sampling in the early part of the record. To calculate a monthly anomaly we first calculated monthly mean ozone at a particular site for the entire time series, and then calculated the 16-year mean for all 12 months of the year over the base period 1995–2010. The difference between the observed monthly mean and the 16-year monthly mean for the same month yields the monthly anomaly.
Trends are estimated with the following linear regression model:(1)
Where y is the monthly mean ozone anomaly, t is a monthly index from January 1957 to December 2018, α is a constant, β is a linear trend, γ and δ are coefficients for a 12-month harmonic series of seasonal cycle (M = 1,…, 12), and Rt is AR(1) to account for autocorrelation, i.e. Ri = ρRt–1 + ∈t with ∈t a normal random error series. The sine and cosine terms account for any residual seasonal signal that may remain in the monthly anomalies. Equation (1) follows the form of standard statistical methods for calculating trends in time series of environmental data characterized by seasonal cycles and autocorrelation [Cochrane and Orcutt, 1949; Weatherhead et al., 1998; Chandler and Scott, 2011]. This method is appropriate for long time series and the estimated trends are not disproportionately affected by outliers as the time series are comprised of at least twenty years of monthly values. Trends are reported with 95% confidence intervals and p-values. The p-value is the probability under a specified statistical model that a statistical summary of the data would be equal to or more extreme than its observed value. Following the recent recommendation of the American Statistical Association [Wasserstein and Lazar, 2016; Wasserstein et al., 2019] we do not treat p < 0.05 as a “bright-line” to label a trend as statistically significant or meaningful. Trend values are reported regardless of p-value, and some of the figures follow the TOAR color scheme for indicating the p-value of a particular ozone time series [Fleming and Doherty et al., 2018; Gaudel et al., 2018; Mills et al., 2018].
The Supplemental Material illustrates the degree to which trends can differ when they are based on simple linear regression of observed monthly means, versus the linear regression model (1) and monthly anomalies. For example, at Tustervatn, Norway (Figure S-1a) the ozone trend based on the observed monthly mean is 0.6 ± 0.9 ppbv decade–1 (p = 0.17), while the trend based on anomalies is stronger with tighter confidence limits, 0.9 ± 0.8 ppbv decade–1 (p = 0.02). Minamitorishima, is a very small island at the edge of the tropics in the North Pacific Ocean (Figure S-1b), impacted by Asian outflow during the winter months [Wada et al., 2011]. The trend at Minamitorishima based on observed monthly means indicates an ozone decrease of 14% (–1.7 ± 1.8 ppbv decade–1; p = 0.07) from 1994 to 2018. However, the trend based on anomalies shows a weaker decrease of only 3% (–0.6 ± 0.8 ppbv decade–1; p = 0.17). In addition, the monthly anomalies reveal repeated cycles of ozone increases and decreases that are not evident from the observed monthly means. The ozone fluctuations at Minamitorishima are related to shifting transport patterns produced by climate variability [Okamoto et al., 2018].
Monthly anomaly time series and their associated linear trend values are shown for all sites in Appendix S-B. These plots also show the results of the locally weighted regression (or lowess, or loess) method, which is used to describe the multi-year ozone fluctuations at each site [Cleveland, 1979; Cleveland and Devlin, 1988]. The lowess smoother fits are not used for a formal trend estimate, instead they represent a method for estimating a regression surface through a multivariate smoothing procedure, fitting the monthly ozone anomalies to the most attributable long term variability in the time series, in a moving fashion analogous to how a moving average is computed for a time series. The attributable long-term variability is subjective and for our purposes we selected a time scale of 10 years for examining ozone variability. A comparison of our selected lowess smoother to one that is sensitive to a shorter time scale, and to a similar low pass, filter-based fast Fourier transform is presented in Appendix S-A. As shown in Appendix S-B, the lowess smoother can be used to identify multi-year periods of ozone increases and decreases not detected by the linear regression model. In most cases the linear trend provides an adequate description of the long-term rate of change; clear exceptions are, 1) Zugspitze, which can be summarized by a strong upward trend (6.4 ± 1.1 ppb decade–1, p ≤ 0.01) over 1978–1997, and a weak downward trend (–1.2 ± 1.0 ppb decade–1, p = 0.01) over 1998–2017; 2) Centennial, which exhibits a sharp drop in 2004; 3) Jungfraujoch which experienced several years of anomalously low ozone in the early 1990s; and 4) Izaña, where ozone increased abruptly in the late 1990s.
Appendix S-A in the Supplemental Material provides an evaluation of polynomial fits, which have been used in previous research (e.g. Logan et al., 2012; Parrish et al., 2014) to estimate long-term ozone trends. The idea of a polynomial fit is analogous to gradually adding “nodes” to the trend estimate, with each additional term of the polynomial equation adding another bend to the curve, thus one or multiple change(s) in the trend can be revealed in the resulting estimate. However, due to the challenges of fitting polynomials to highly variable tropospheric ozone time series (described below) they are not as effective as the lowess smoother for identifying the multi-year ozone variability common to tropospheric ozone observations. Here we provide a brief summary of two of the most severe problems associated with polynomial fits, and the reader is referred to Appendix S-A for further details.
The focus of this study is to quantify long-term ozone trends worldwide, at as many remote monitoring sites as possible. We require each site to have at least 20 years of data, beginning no later than 1995 and extending to the present (2013–2018). Sites must be in remote locations far from fresh anthropogenic emissions, which could lead to localized production or destruction of ozone [Escudero et al., 2014; Simon et al., 2015; Strode et al., 2018]. The TOAR Surface Ozone Database, which holds ozone metrics from more than 9,000 sites worldwide [Schultz et al., 2017], was scanned for sites that meet these criteria, yielding the 27 remote surface sites reported in Table 1. Twenty sites are in the Northern Hemisphere and seven are in the Southern Hemisphere; six sites are in the polar regions and two are in the tropics; thirteen sites are high elevation (>1500 m), of which eight are mountaintop sites; six sites are influenced by the marine boundary layer due to their island or coastal locations (see Table 1 for a listing of the sites in each of these environments). The diurnal ozone cycle at each site was examined to select the time of day when atmospheric conditions are well-mixed. This criterion typically resulted in daytime (08:00 to 19:59 solar time) data being selected for low elevation sites, to avoid the nighttime hours when ozone is likely to be depleted under the nighttime temperature inversion. Conversely, nighttime (20:00 to 07:59 solar time) data were selected for mountaintop sites to focus on regionally representative ozone, and to avoid local air masses with depleted ozone that are transported from the valleys to the mountaintops under daytime upslope wind conditions [Price and Pales, 1963; Weiss-Penzias et al., 2006; Gheusi et al., 2011; Gallagher et al., 2012; Cristofanelli et al., 2013]. The mountaintop sites in this analysis are Mauna Loa, Hawaii [Oltmans et al., 1986]; Zugspitze [Gilge et al., 2010], Jungfraujoch [Cui et al., 2011] and Sonnblick [Gilge et al., 2010] in the Alps; Mt. Waliguan in central China [Xu et al., 2016]; Kislovodsk High Mountain Station in southern Russia [Tarasova et al., 2009]; Izaña on the island of Tenerife in the Canary Islands [Cuevas et al., 2013]; and El Tololo in the Andes Mountains of Chile [Anet et al., 2017]. In the case of Kislovodsk High Mountain Station, which has a weak diurnal cycle, 24-hour data were used due to limited sampling in the early part of the record. Some sites, such as those in the polar regions (e.g Zeppelin [Solberg, 2003]) or those in the marine boundary layer (e.g. American Samoa), have virtually no diurnal ozone cycle and therefore data from day or night, or all 24 hours of the day can be used. The time of day selected for each site is indicated in Tables 2 and 3.
|Site name||Full record, beginning 1971–1990||Full record, beginning 1991–1994||Since 1995||Since 2000|
|Remote sites in the Northern Hemisphere|
|Alert (D)||0.1 ± 0.8 p = 0.72||–0.5 ± 0.9 p = 0.29||–0.5 ± 1.5 p = 0.47|
|Zeppelin (D)||0.6 ± 0.7 p = 0.06||0.3 ± 1.0 p = 0.52||–0.7 ± 1.2 p = 0.23|
|Barrow (24)||0.6 ± 0.3 p = 0.00||0.8 ± 0.9 p = 0.08||1.0 ± 1.4 p = 0.16|
|Esrange (D)||0.8 ± 0.7 p = 0.04||0.0 ± 0.8 p = 0.92||0.0 ± 1.2 p = 0.97|
|Tustervatn (D)||0.9 ± 0.8 p = 0.02||–0.6 ± 0.7 p = 0.12||–1.4 ± 1.0 p = 0.00|
|Denali (D)||0.7 ± 0.6 p = 0.01||0.7 ± 0.9 p = 0.14||1.1 ± 1.3 p = 0.10|
|Strath Vaich Dam (D)||0.2 ± 0.7 p = 0.49||–0.4 ± 1.0 p = 0.42||–0.7 ± 1.5 p = 0.34|
|Mace Head (D)||1.1 ± 0.5 p = 0.00||0.7 ± 0.8 p = 0.08||0.6 ± 0.9 p = 0.18|
|IAGOS, 650 hPa (24)||1.3 ± 0.8 p = 0.00||1.2 ± 0.8 p = 0.00||1.2 ± 1.0 p = 0.02|
|Zugspitze (N)||2.3 ± 0.7 p = 0.00||–0.8 ± 0.6 p = 0.00||–0.6 ± 0.8 p = 0.13|
|Sonnblick (N)||0.0 ± 0.6 p = 0.98||–1.0 ± 0.7 p = 0.00||–1.8 ± 0.9 p = 0.00|
|Jungfraujoch (N)||1.1 ± 0.6 p = 0.00||0.2 ± 0.6 p = 0.45||–0.2 ± 0.7 p = 0.66|
|Kislovodsk (24)||–3.4 ± 1.5 p = 0.00||–1.1 ± 1.6 p = 0.17||0.5 ± 2.0 p = 0.61|
|Centennial (D)||–0.6 ± 0.9 p = 0.16||–1.5 ± 1.2 p = 0.01||–2.6 ± 1.8 p = 0.00|
|Great Basin (D)||0.5 ± 0.9 p = 0.26||0.2 ± 1.0 p = 0.67||–0.5 ± 1.4 p = 0.48|
|Gothic (D)||–1.0 ± 0.6 p = 0.00||–1.9 ± 0.8 p = 0.00||–2.8 ± 1.1 p = 0.00|
|Grand Canyon (D)||–0.3 ± 0.7 p = 0.33||–1.5 ± 0.8 p = 0.00||–2.6 ± 1.1 p = 0.00|
|Mt. Waliguan (N)||1.8 ± 0.5 p = 0.00||1.7 ± 0.5 p = 0.00||1.6 ± 0.8 p = 0.00|
|Izaña (N)||1.3 ± 0.6 p = 0.00||0.5 ± 0.9 p = 0.28||0.3 ± 1.0 p = 0.55|
|Minamitorishima (N)||–0.6 ± 0.8 p = 0.17||–0.4 ± 0.9 p = 0.35||0.5 ± 1.2 p = 0.38|
|MLO–all (N)||1.3 ± 0.5 p = 0.00||0.9 ± 1.4 p = 0.20||1.3 ± 2.1 p = 0.23|
|MLO-low humidity (N)||2.1 ± 0.4 p = 0.00||2.4 ± 1.0 p = 0.00||3.3 ± 1.5 p = 0.00|
|MLO-high humidity (N)||1.0 ± 0.3 p = 0.00||0.6 ± 0.9 p = 0.16||0.4 ± 1.3 p = 0.51|
|Remote sites in the Southern Hemisphere|
|American Samoa (24)||0.2 ± 0.2 p = 0.05||1.5 ± 0.7 p = 0.00||2.2 ± 0.9 p = 0.00|
|El Tololo (N)||0.2 ± 0.6 p = 0.52||0.2 ± 0.9 p = 0.63|
|Cape Point (24)||1.6 ± 0.3 p = 0.00||1.2 ± 0.6 p = 0.00||0.9 ± 0.9 p = 0.05|
|Cape Grim (D)||0.4 ± 0.2 p = 0.00||0.3 ± 0.3 p = 0.08||–0.2 ± 0.4 p = 0.27|
|Ushuaia (D)||–0.9 ± 0.5 p = 0.00||–0.9 ± 0.5 p = 0.00||–0.8 ± 0.6 p = 0.00|
|Neumayer (D)||1.0 ± 0.4 p = 0.00||0.8 ± 0.6 p = 0.01|
|South Pole (24)||0.3 ± 0.4 p = 0.16||1.5 ± 0.6 p = 0.00||1.0 ± 0.7 p = 0.00|
|Rural sites in the boundary layer of southern Germany|
|Pfälzerwald-Hort. (D)||0.2 ± 0.8 p = 0.69||–0.9 ± 1.0 p = 0.07||–0.6 ± 1.4 p = 0.40|
|Hohenpeissenberg (D)||1.8 ± 0.5 p = 0.00||–1.3 ± 1.0 p = 0.02||–2.2 ± 1.5 p = 0.00|
|Schwarzwald-Süd (N)||–2.4 ± 1.1 p = 0.00||–2.2 ± 1.4 p = 0.00||–1.0 ± 1.6 p = 0.21|
|Site name||Full record, beginning 1971–1990||Full record, beginning 1991–1994||Since 1995||Since 2000|
|Remote sites in the Northern Hemisphere|
|Alert (D)||0.4 ppbv, 1%||–1.2 ppbv, –3%||–1.0 ppbv, –3%|
|Zeppelin (D)||1.8 ppbv, 5%||0.7 ppbv, 2%||–1.2 ppbv, –4%|
|Barrow (24)||2.6 ppbv, 12%||1.9 ppbv, 6%||1.8 ppbv, 7%|
|Esrange (D)||2.0 ppbv, 7%||0.1 ppbv, 0%||0.0 ppbv, 0%|
|Tustervatn (D)||2.6 ppbv, 9%||–1.3 ppbv, –4%||–2.4 ppbv, –6%|
|Denali (D)||2.2 ppbv, 8%||1.5 ppbv, 4%||1.8 ppbv, 6%|
|Strath Vaich Dam (D)||0.7 ppbv, 2%||–0.9 ppbv, –3%||–1.2 ppbv, –3%|
|Mace Head (D)||3.1 ppbv, 8%||1.5 ppbv, 4%||1.0 ppb, 3%|
|IAGOS, 650 hPa (24)||2.9 ppbv, 6%||2.6 ppbv, 7%||2.1 ppbv, 5%|
|Zugspitze (N)||9.1 ppbv, 26%||–1.8 ppbv, –4%||–1.1 ppbv, –2%|
|Sonnblick (N)||0.0 ppbv, 0%||–2.1 ppbv, –5%||–2.9 ppbv, –7%|
|Jungfraujoch (N)||3.5 ppbv, 5%||0.5 ppbv, 1%||–0.3 ppbv, –1%|
|Kislovodsk (24)||–8.2 ppbv, –17%||–2.0 ppbv, –5%||0.7 ppbv, 2%|
|Centennial (D)||–1.8 ppbv, –3%||–3.2 ppbv, –8%||–4.4 ppbv, –10%|
|Great Basin (D)||1.3 ppbv, 3%||0.5 ppbv, 2%||–0.8 ppbv, –2%|
|Gothic (D)||–2.7 ppbv, –5%||–4.3 ppbv, –10%||–4.8 ppbv, –11%|
|Grand Canyon (D)||–1.0 ppbv, –2%||–3.4 ppbv, –9%||–4.4 ppbv, –11%|
|Mt. Waliguan (N)||4.0 ppbv, 9%||3.6 ppbv, 8%||2.6 ppbv, 6%|
|Izaña (N)||3.9 ppbv, 8%||1.1 ppbv, 3%||0.5 ppbv, 1%|
|Minamitorishima (N)||–1.4 ppbv, –3%||–0.9 ppbv, –2%||1.0 ppbv, 3%|
|MLO–all (N)||5.9 ppbv, 16%||2.0 ppbv, 6%||2.3 ppbv, 6%|
|MLO-low humidity (N)||9.1 ppbv, 24%||5.4 ppbv, 13%||5.9 ppbv, 12%|
|MLO-high humidity (N)||4.3 ppbv, 14%||1.4 ppbv, 5%||0.8 ppbv, 2%|
|Remote sites in the Southern Hemisphere|
|American Samoa (24)||0.9 ppbv, 7%||2.9 ppbv, 37%||3.2 ppbv, 54%|
|El Tololo (N)||0.4 ppbv, 1%||0.3 ppbv, 1%|
|Cape Point (24)||5.5 ppbv, 37%||2.7 ppbv, 20%||1.5 ppbv, 9%|
|Cape Grim (D)||1.6 ppbv, 10%||0.6 ppbv, 3%||–0.4 ppbv, –2%|
|Ushuaia (D)||–2.1 ppbv, –13%||–2.0 ppbv, –14%||–1.4 ppbv, –9%|
|Neumayer (D)||2.1 ppbv, 13%||1.3 ppbv, 10%|
|South Pole (24)||1.3 ppbv, 5%||3.4 ppbv, 14%||1.8 ppbv, 7%|
|Rural sites in the boundary layer of southern Germany|
|Pfälzerwald-Hort. (D)||0.4 ppbv, 2%||–2.2 ppbv, –10%||–1.0 ppbv, –4%|
|Hohenpeissenberg (D)||8.1 ppbv, 48%||–2.8 ppbv, –9%||–3.7 ppbv, –11%|
|Schwarzwald-Süd (N)||–6.7 ppbv, –18%||–5.1 ppbv, –15%||–1.8 ppbv, –5%|
Every surface site selected for this analysis was screened to ensure its remote location, using information provided by the TOAR Surface Ozone Database. The first step was to identify all rural sites with data spanning 1995–2015, using an objective algorithm developed by TOAR [Schultz et al., 2017]. This algorithm takes advantage of several global gridded geo-data sets (human population density, satellite-detected tropospheric column NO2, a bottom-up NOx emission inventory, satellite-detected nighttime lights of the world, and satellite-detected land cover), which are cross-referenced with the locations of each site in the TOAR database. Using thresholds of human population, satellite-detected tropospheric column NO2, and satellite-detected nighttime lights of the world, the algorithm identified 400 rural sites in the Northern Hemisphere and just 8 in the Southern Hemisphere. Next, the JOIN web interface (https://join.fz-juelich.de) was used to visually inspect the surroundings of each rural site, as revealed by current satellite imagery (provided by Google maps; see Schultz et al.  for further details), to identify the sites in remote settings. All sites are more than 100 km from large urban areas, with the exception of the three Alpine sites and Cape Point. As described below the data at these sites were filtered by time of day (Alpine sites) or wind direction (Cape Point) to limit the influence from nearby urban areas.
Sections 2.3.1 through 2.3.6 provide additional information on selected sites to describe unique data filtering methods, historical observations, or site characteristics that may influence interpretation of the ozone time series. Three additional sites from the rural German boundary layer are described in Section 2.3.7. These sites are not remote, and they are shown to provide context to the ozone trends observed at the high altitude Alpine sites. Finally, Section 2.3.8 described the IAGOS commercial aircraft observations above Western Europe. Focus is placed on the observations at 650 hPa to demonstrate that the IAGOS data reveal the ozone trend in the lower free troposphere above Europe, while ozone observations at the same altitude in the Alps are impacted by the European boundary layer.
The longest continuous time series of surface ozone observations in remote locations are from the four baseline observatories maintained by the NOAA Global Monitoring Laboratory (GML) [Oltmans et al., 1986]: Barrow Atmospheric Baseline Observatory (BRW) on the northern coast of Alaska, near the small town of Utqiaġvik (71.3° N, –156.6° E, 11 m); Mauna Loa Observatory (MLO) on the Big Island of Hawaii (19.5° N, –155.6° E, 3397 m); American Samoa Observatory (SMO) in the tropical South Pacific Ocean (14.3° S, –171.6° E, 42 m); and South Pole Observatory (SPO) at the geographical South Pole (90.0° S, 59.0° E, 2840 m). Surface ozone observations began in 1973 at BRW and MLO, and in 1975 at SMO and SPO [Oltmans, 1981]. Prior to 1975, ozone was measured using an electrochemical concentration cell (ECC) meter, which depends on the oxidation-reduction of potassium iodide to measure ozone. In 1975 the measurement technique was updated to the modern UV-absorption method. As described by Oltmans , concurrent measurements using both methods were conducted to ensure time series consistency. Ozone observations at American Samoa were suspended in January, 2016, but may resume at a later date.
Historical ozone observations are available at MLO and SPO and are reported here in order to extend the MLO and SPO time series as far back in time as possible. Ozone was first measured at MLO over a 2-year period from August, 1957 to July, 1959 [Price and Pales, 1963] using the Regener Automatic instrument, based on the Ehmert technique [Bowen and Regener, 1951]. As discussed by TOAR [Tarasick and Galbally et al., 2019], the Ehmert technique is a wet chemical method that uses a neutral buffered sampling solution containing iodide and thiosulfate (S2O32-). The technique is reliable and compares very well to the UV-absorption method [Tarasick and Galbally et al., 2019]. A Regener Automatic instrument also measured ozone at SPO from February 1961 to July 1963 [Oltmans and Komhyr, 1976a, b].
MLO is located at the interface between the tropics and mid-latitudes, and is therefore influenced by both easterly tropical air masses and westerly mid-latitude air masses [Harris and Kahl, 1990; Oltmans et al., 2006]. The frequency of these air masses varies with time of year and on interannual and even decadal time scales due to unforced short-term climate variability associated with El Niño/Southern Oscillation (ENSO) and the Pacific-North American pattern [Lin et al., 2014]. Ozone is typically greater in the mid-latitude air masses, and the long term trend at MLO is affected by the relative frequency of air mass transport from high and low latitudes in response to climate variability [Lin et al., 2014]. To reduce the noise in the long-term ozone trend due to climate variability we apply an air-mass classification method for examining ozone trends at MLO, previously used by the NOAA State of the Climate reports [Arndt et al., 2018] and described in detail by the Tropospheric Ozone Assessment Report [Gaudel et al., 2018]. Co-located dewpoint observations are used to separate the ozone observations into low humidity air samples, representative of mid-latitude air masses that originate at higher altitudes and higher latitudes, and high humidity air samples, representative of tropical air masses from lower latitudes and lower altitudes.
Ozone was measured at the summit of Zugspitze (2960 m) in the Alps of southern Germany from 1978 to 2010 by the late H.-E. Scheel of the Fraunhofer Institute (IFU) and the Karlsruher Institut für Technologie, Garmisch-Partenkirchen, Germany [Scheel et al., 1997]. These data have been widely reported in the literature [Oltmans et al., 2006; Gilge et al., 2010; Logan et al., 2012; Gaudel et al., 2018] and are available from the TOAR Surface Ozone Database. A chemiluminescence instrument was used from 1978 to 1996, when a UV-absorption instrument was installed [Logan et al., 2012]. The two instruments overlapped for three years and the data from the two methods were found to have similar accuracy, according to WMO/GAW audits [Herzog et al., 1996]. In particular, the long-term stability of the sensitivity of the chemiluminescence instrument (Bendix 8002) has been comparable or even better than the stability of the different UV instruments used at the site. In 2000 the German Federal Environment Agency (UBA) commenced ozone measurements from the Schneefernerhaus station (2656 m), 300 m below the Zugspitze summit [Gilge et al., 2010], however the record in the TOAR Surface Ozone Database begins in 2002. Comparison of the overlapping time period shows that the summit and Schneefernerhaus ozone records are very similar in terms of diurnal, seasonal and interannual variations, with the main difference being that the Schneefernerhaus ozone values are slightly lower [Zellweger et al., 2011]. To estimate the ozone trend at Zugspitze from 1978 to the present, the summit and Schneefernerhaus ozone anomaly records must be merged. A complication arises because reference ozone values spanning the 1995–2010 base period can’t be calculated for the Schneefernerhaus record, which only begins in 2002. Therefore, the following procedure was employed. First, monthly mean nighttime ozone at Schneefernerhaus was compared to the corresponding summit values for the period 2002–2010. Due to its lower elevation, ozone at Schneefernerhaus is 1.3 ppbv less than the summit values, on average. Monthly ozone anomalies were calculated at the summit site using the summit’s 1995–2010 base period. The summit ozone base period was then reduced by 1.3 ppbv (making the two overlapping times series virtually indistinguishable from each other) and used to calculate monthly ozone anomalies at Schneefernerhaus. The two monthly ozone anomaly records could then be merged, using 1978–2001 data from the summit, and 2002–2016 data from Schneefernerhaus.
The monitoring site of Mace Head, Ireland, is situated in a very rural area, 50 km west of Galway, the largest municipality in the region (population, 80,000). While this site on the western edge of Europe often samples aged marine boundary layer air from the North Atlantic Ocean, it is also impacted by air masses containing aged pollution from Europe [Derwent et al., 2007]. Previous studies have filtered the Mace Head data using co-located trace gas observations or back trajectories to remove the influence from distant European emissions [Derwent et al., 2018], resulting in a different trend for the filtered data compared to the full unfiltered record. For the present analysis the full unfiltered ozone record has been utilized, although nighttime data were omitted to avoid observations affected by local nighttime deposition. Therefore, the ozone trends reported for Mace Head are influenced by both the marine boundary layer and aged air masses from Europe. Comparison of the daytime ozone observations to the baseline values reported by Derwent et al.  shows that both data sets have similar seasonal cycles, with the annual mean baseline ozone being approximately 2 ppbv greater than the unfiltered daytime data. Derwent et al.  concluded that coarse resolution global models (e.g. 2° × 2.5°) may have difficulty in simulating the recirculation of aged air masses from Europe to Mace Head, and recommended that these particular models be evaluated against the filtered time series. Looking forward, the most recent generation of global atmospheric chemistry models are run at much higher resolution (e.g. 1° × 1°, or finer) [Ziemke et al., 2019; He et al., 2020], and therefore evaluating these models against the full unfiltered ozone record will test their ability to replicate ozone levels in the aged European plumes.
Another coastal monitoring site used in this analysis is Cape Point, South Africa. This site is not remote due to its proximity to Cape Town Metropolitan Municipality, 25 km to the north (population 4.0 million). However, the station’s principal investigator uses observed wind direction to filter the data set and omit ozone observations influenced by recent emissions from the nearby urban area, equal to 22% of the total data set [Brunke et al., 2004]. The subset of data filtered by wind direction is used for this analysis; no other remote ozone time series in the TOAR database was archived with a full time series and a subset filtered by wind direction. Due to the filtering of this time series by wind direction these ozone observations are representative of the air masses originating to the west of Cape Point. Therefore, when comparing this filtered time series to a global chemistry-climate model we recommend that the model grid cell chosen for evaluation be located to the west of Cape Point, where recent continental outflow is infrequent.
Australia’s Cape Grim Baseline Air Pollution Station is located on a rural coastal bluff in northwestern Tasmania and was established in 1976 [Derek et al., 2016]. The ozone monitoring program commenced in 1976 and surface ozone data with quality assured measurements have been obtained since 1982 [Galbally et al., 2000]. The Cape Grim ozone record is the longest mid-latitude record available from the Southern Hemisphere and it is an important data set for monitoring ozone changes in this part of the world. While the air sampled at Cape Grim generally approaches from the Southern Ocean to the west, the observed ozone can often be modified due to influence from the boundary layer of Australia or Tasmania. Molloy and Galbally  used co-located observations of radon, wind speed, wind direction and condensation nuclei to filter 10 years (1992–2001) of Cape Grim ozone data to identify baseline transport conditions from the Southern Ocean (wind and radon data are available from the TOAR database). They found that approximately 40% of the data set was representative of baseline conditions and that the positive ozone trend was approximately 8% greater in baseline air compared to the full data set for those years. The data set used here is the recently produced 1982–2017 Cape Grim surface ozone on the WMO GAW/BiPM standard scale, available at the World Data Centre for Reactive Gases (https://www.gaw-wdcrg.org/). This record has not yet been selected for baseline conditions.
The Izaña high mountain Observatory (28.3° N, –16.5° E, 2367 m), Canary Islands, located in the subtropical North Atlantic Ocean under the descending branch of the Hadley cell (around 30° N), is representative, most of the time, of free-tropospheric background conditions [Cuevas et al., 2013]. These conditions are fully assured during nighttime (20:00–08:00 UTC) when katabatic flow conditions predominate. Surface ozone measurements began in 1987 in the framework of what is now the WMO/GAW program. Surface ozone quality assurance is maintained with periodic audits carried out by Empa, The Swiss Federal Laboratories for Materials Science and Technology (6 in total, with a seventh in progress, WCC-Empa (2019)).
The free troposphere background conditions at Izaña are characterized by the presence of air masses from the mid-troposphere over the central and western North Atlantic Ocean, with relatively high ozone values because they are frequently impacted by upper tropospheric air masses throughout their trajectories [Prospero et al., 1995; Oltmans et al., 1996; Rodríguez et al., 2004; Rodríguez and Cuevas, 2013], or by strong stratosphere-troposphere exchange processes, driven by deep lows and cut-off lows north of the Canary Islands [Kentarchos et al., 2000; Cuevas et al., 2013]. The opposite situation occurs with the arrival of Saharan air masses, characterized by low ozone values [Cuevas et al., 2013]. The low ozone values are partly due to a low latitude origin within the North African continental boundary layer, and partly due to these air masses having a high mineral dust content, and relatively high water vapor (in contrast to clean free troposphere conditions), that lead to ozone destruction [Andrey et al., 2014]. The impact of each of these two factors on the observed ozone is still an open question. Therefore, tropospheric ozone interannual variability and trends at Izaña are modulated not only by changes in tropospheric chemistry, but also by changes in natural atmospheric processes such as baroclinic events that favor ozone enrichment in the mid- and upper troposphere, and those that modulate the frequency and intensity of the Saharan Air Layer intrusions over the subtropical North Atlantic, mainly in summer, which cause ozone reduction. These processes are, in turn, modulated by changes in large-scale processes and meteorological patterns, such as mid-latitude Rossby waves, the Saharan Heat Low, and the North African Dipole Intensity [Rodríguez et al., 2015; Cuevas et al. 2017]. The ozone trend at Izaña was previously found to be 0.19 ± 0.05% yr–1 for the period 1988–2009 [Cuevas et al., 2013].
Three long-term ozone monitoring sites located at relatively low elevations in the southern German boundary layer were selected for comparison to the high elevation Alpine sites: Hohenpeissenberg, Schwarzwald-Süd and Pfälzerwald-Hortenkopf (Table 1). The sites are in rural locations and unlikely to be influenced by fresh NO emissions, which destroy ozone. However, the sites are impacted by aged boundary layer pollution and the long-term trends at these sites reflect ozone levels as they have responded to changing ozone precursor emissions within Germany and neighboring countries.
As detailed in Section 3.3 below, Alpine mountain sites, which have previously been used to assess long-term ozone changes in the free troposphere over Europe, show significant impacts from aged regional pollution. A more robust estimate of lower free tropospheric ozone changes can be obtained from frequent commercial aircraft observations. Since 1994 the In-Service Aircraft for the Global Observing System (IAGOS) program (formerly known as MOZAIC, 1994–2011) has measured ozone worldwide, using instruments onboard commercial aircraft of internationally operating airlines [Marenco et al., 1998; Petzold et al., 2015; http://www.iagos.org]. Ozone is measured using a dual-beam UV-absorption monitor (time resolution of 4 seconds) with an accuracy estimated at about ± (2 nmol mol–1 + 2%) [Thouret et al., 1998; Nédélec et al., 2015]. Because most IAGOS aircraft have belonged to airlines based in Europe since the program began in 1994, Western Europe is the program’s most frequently sampled region of the world. Above northwestern Europe (0°–15° E, 47°–55° N) IAGOS aircraft measured 34,600 ozone profiles between 1994 and 2016, with 99% of profiles from Frankfurt, Paris, Munich, Brussels, Dusseldorf and Amsterdam. The lower tropospheric portions of the profiles have been shown to be regionally representative of ozone across Western Europe [Petetin et al., 2018]. The sampling frequency varies according to airline schedules, but on average, four profiles are recorded somewhere in this region every day. Previous analysis has shown that 12 profiles per month can produce monthly mean ozone values in the free troposphere with an uncertainty less than 5–10% [Saunois et al., 2012], which demonstrates that the high sampling frequency by IAGOS aircraft above Western Europe can easily produce accurate monthly mean ozone profiles. IAGOS aircraft can take-off and land at any time of day and all data are used in this analysis. No diurnal ozone cycle occurs in the free troposphere above Europe (above the 750 hPa level), although a clear ozone cycle occurs in the boundary layer, and is strongest below 950 hPa [Petetin et al., 2016]. For this analysis ozone trends are estimated for several pressure levels from 950 to 250 hPa, which avoids the lowest layers with very strong diurnal cycles. Any data points in the stratosphere were removed from the analysis, as determined from the potential vorticity values associated with each ozone profile, and available from the IAGOS data portal (https://doi.org/10.25326/20). Particular attention is given to the ozone trend at 650 hPa because this pressure surface resides in the lower free troposphere, and because it is close to the average pressure of the high elevation ozone monitor at the summit of Jungfraujoch (located at 3580 m above sea level with an annual average pressure of 655 hPa, based on observations by MeteoSwiss, as reported in the TOAR Surface Ozone Database).
Following the methods of Schultz  and Weiss-Penzias et al.  this analysis also takes advantage of IAGOS observations of relative humidity, temperature and pressure to calculate vertical profiles of specific humidity. Relative humidity was measured by the MOZAIC Capacitive Hygrometer (1994–2011) [Helten et al., 1998; Neis et al., 2015a] and the IAGOS Capacitive Hygrometer (2011-present) [Neis et al., 2015b]. These observations are used to estimate the quantity of European boundary layer air at the summit of Jungfraujoch. We used the observed monthly median specific humidity values in the boundary layer and at 650 hPa, as measured by IAGOS (Figure S-2), to answer the question: How much air from the European boundary layer must be mixed with free tropospheric air at 650 hPa to achieve the same specific humidity values as Jungfraujoch? These calculations were based on simple linear mixing ratio relationships, with the assumption that specific humidity is a conserved tracer. However, specific humidity is not entirely conserved within an air mass ascending from the boundary layer to a pressure level of 650 hPa, because some of the moisture will be lost through precipitation. Therefore, estimates of the percentage of boundary layer air at the summit of Jungfraujoch are considered to be a lower bound.
Before focusing on ozone trends based on monthly anomalies, we first illustrate the range of ozone values that can be found at remote locations around the world, in terms of the seasonal cycle, interannual variability, multi-year fluctuations and long-term trends. We examine ambient monthly mean ozone values at the four sites that provide the longest continuous ozone time series at remote locations (40+ years), beginning in either 1973 or 1975: Barrow Atmospheric Baseline Observatory, Mauna Loa Observatory (MLO), American Samoa Observatory and South Pole Observatory. Trends from these sites are periodically reported in the literature [Oltmans et al. 1994, 1998, 2006, 2013; Arndt et al., 2018; Gaudel et al., 2018], and here we include the most recently available data, along with the reliable historical observations from MLO (1957–1959) and South Pole (1961–1963) to evaluate ozone changes over six decades. These time series are shown in Figure 3 with straight lines fit through the data, based on simple linear regression for illustrative purposes; for time series of this length, the slope of the trend line through the ambient ozone values is very similar to the slope estimated from monthly anomalies, as reported in Tables 2 and 3. Monthly ozone anomalies for each of these sites are shown in Appendix S-B (see Supplemental Material). The two Northern Hemisphere sites show increasing ozone since the 1970s, with the trend at MLO in the tropics being twice as strong as the trend at Barrow in the Arctic. In the Southern Hemisphere, trends at Samoa (tropical South Pacific Ocean) and South Pole are similarly positive and weak, but with South Pole having a much higher p-value (p = 0.22). Extension of the trend lines at MLO and South Pole back to the time of the historical observations shows that ozone at South Pole has changed little since the early 1960s, while ozone at MLO has increased by roughly 50% since the late 1950s (based on an average value of ~30 ppbv in the late 1950s and 45 ppbv in 2018). This increase, on the northern edge of the tropics, is similar to the northern mid-latitude increases reported by Tarasick and Galbally et al. , who compared a range of historical ozone observations at rural sites (made between 1896 and 1975) to modern observations.
Figure 3 also shows that ozone in the low humidity air masses (biased toward a mid-latitude origin) is much greater than ozone in the high humidity air masses (biased toward a tropical origin); see Section 2.3.1 for a description of the method for selecting low and high humidity air samples at MLO. Table 2 shows that ozone in the low humidity air masses has increased at twice the rate of ozone in the high humidity air masses. Specifically, since 1974, ozone has increased in the low humidity air masses at MLO at the rate of 2.1 ± 0.4 ppbv decade–1, for a total increase of 9.1 ppbv or 24% (1974–2018), with the lowess smoother showing only small deviations from the linear regression line (Appendix S-B). As discussed by Gaudel et al. , the low humidity air masses at MLO are more likely to represent mid-latitude air originating to the west (i.e. Asia) than the high humidity air masses which are more likely to come from the tropics and from the east (i.e. Central America). Ozone precursor emission rates are changing rapidly across Asia due to economic forces and air quality control policies, with increases in some regions and decreases in others [Zhang et al., 2016; Lin et al., 2017; Miyazaki et al., 2017; van der A et al., 2017; Hoesly et al., 2018]. Therefore, further modelling work is required to quantify the impact of changing Asian emissions on the MLO ozone trend.
Focus is now shifted to all 27 remote surface sites in an attempt to assess long-term surface ozone trends on the global scale. Trends are also assessed for the IAGOS aircraft observations at 650 hPa above Western Europe, and for the low and high humidity air masses observed at MLO (see anomaly time series plots in Appendix S-B). The lowess fits to each of these time series are shown in Figure 4, comparing the ozone fluctuations for all sites in northern high latitudes, northern mid-latitudes, the tropics and the southern extra-tropics. The lowess fits demonstrate the variability that is found among sites even in the same latitude bands. For example, in the northern polar region both Zeppelin and Tustervatn show a strong increase of ozone from 1990 until 2004, followed by a strong decrease, a pattern not seen at the other four sites. At northern mid-latitudes most sites show an increase of ozone during the 1990s, but since 2000 the time series diverge with some showing increases and others decreases. In the tropics the dry air masses at MLO are unique as they show a steady increase from 1973 to 2018, while Minamitorishima has a repeated cycle not seen at the other sites. In the southern extra-tropics the time series have diverged since 2010 with half showing increasing ozone and the other half showing decreases.
Figure 5 shows the ozone trends for each time series with an arrow-based approach, used previously by Cooper et al.  and by TOAR [Fleming et al., 2018; Gaudel et al., 2018; Mills et al., 2018]. The figure reports trends (based on monthly anomalies) through the most recently available year, but beginning in two different time periods: 1) 21 sites that began between 1974 and 1990; and 2) all 27 sites since 1995. The corresponding numeric values of the trends, including confidence intervals and p-values, are reported in Tables 2 and 3. Because trends since 1995 are available for all sites, and because this time period is longer than 20 years (necessary to overcome the influence of periodic climate variability [Barnes et al., 2016]) the main conclusions from this analysis are based on trends since 1995. As a first step towards periodically documenting 21st century ozone trends, and for comparison to the global trends reported by TOAR-Climate, Figure S-3 shows trends beginning in the year 2000.
Northern Hemisphere trends since 1974–1990 are mainly positive with 11 of 17 time series showing positive trends in the range of 0.6–2.3 ppbv decade–1 (p-values less than 0.10). Two time series have negative trends (p-values less than 0.10) occurring in the Caucasus Mountains of southern Russia (Kislovodsk) and the high elevations of the western USA (Gothic in Colorado). Only 4 sites are available from the Southern Hemisphere, all tending towards increasing ozone, with the strongest trends at the mid-latitude sites of Cape Grim and Cape Point (0.4–1.6 ppbv decade–1; p-value < 0.05). Trends are positive but weak at American Samoa (0.2 ± 0.2 ppbv decade–1; p = 0.05) and at South Pole (0.3 ± 0.4 ppbv decade–1; p = 0.16).
Northern Hemisphere trends since 1995 are nearly evenly split with 5 of 23 time series having positive trends (p < 0.10), and 5 sites having negative trends (p < 0.10). The remaining sites show no clear indication of a trend. The positive trends occurred in the Arctic, western Ireland, Western Europe (IAGOS observations), central China and in the low humidity air masses at MLO, while the negative trends are clustered in the western USA and the Alps. Section 4 provides some discussion of the variable ozone trends at northern mid-latitudes and places these trends in the context of free tropospheric trends, which are less variable and predominantly positive. To understand if the trends vary seasonally, Supplemental Figure S-4 shows results for all four seasons. In general, the latitudinal variation of trends is similar in all seasons, however the magnitude and sign of the trends can vary greatly from one season to the next. For example, in the Northern Hemisphere negative trends dominate during June–July–August, while positive trends dominate during December–January–February.
Since 1995 seven time series are available from the Southern Hemisphere with five having positive trends (p < 0.10), one site (El Tololo) with little or no change, and only the site of Ushuaia in southern Argentina showing a negative trend (p < 0.05). Lu et al.  used a global chemical transport model to explore the impact of the poleward expansion of the Southern Hemisphere Hadley circulation on tropospheric ozone across the Southern Hemisphere. They determined that the observed ozone increases cannot be explained by increases of anthropogenic ozone precursor emissions. Rather, the poleward expansion of the Southern Hemisphere Hadley circulation has changed transport patterns across Southern mid- and high latitudes, and it has also shifted the flux of stratospheric ozone into the troposphere toward higher latitudes. The shifting transport patterns and their redistribution of ozone precursors has produced an environment at mid- and high latitudes that is more conducive to photochemical ozone production, which may partially explain the positive ozone trends at four of the Southern Hemisphere extratropical sites. Further work is required to understand why the trend at Ushuaia is opposite to the other Southern Hemisphere sites. This coastal site is on a peninsula with a small airport runway 500 m to the north and the city of Ushuaia (population 75,000) 5 km to the north. While fresh anthropogenic emissions can affect the site, the frequency is low as the winds are predominantly westerly, guided by the mountainous terrain bordering the Beagle Channel [Adame et al., 2019]. Furthermore, the station operator removes observations from the ozone record when the site is impacted by air mass transport from the city. Adame et al. , conducted a transport climatology for Ushuaia based on back-trajectories and found that during all seasons the site is impacted by air masses transported from the mid- and high latitudes of the South Pacific Ocean and from Antarctica. This extensive source region is virtually devoid of anthropogenic or biomass burning emissions, and the seasonal cycle of ozone and CO is consistent with photochemical processes in the remote marine boundary layer where low NOx concentrations lead to net ozone destruction [Galbally et al., 2000]. Therefore, the trend at this site is likely to have greater impact from climate variability than from changes of ozone precursors.
Since 2000 Northern Hemisphere ozone trends have a similar pattern to the trends beginning in 1995, with a range of negative and positive values, but with the rate of change becoming more extreme in some cases (Figure S-3). The wider spread in the range of trend values can be partly explained by the shorter length of the time series (15–18 years) as short-term climate variability (e.g. El Niño/Southern Oscillation) modulates ozone at remote locations due to periodic shifts of transport pathways [Barnes et al., 2016; Fischer et al., 2011; Lin et al., 2014]. Timescales greater than 20 years are typically required to overcome the influence of climate variability. As in the Northern Hemisphere, the pattern of ozone trends in the Southern Hemisphere is similar to that when the time series began in 1995, but with more variability and greater p-values.
This section demonstrates that the IAGOS commercial aircraft observations can be used to quantify the ozone trend in the lower free troposphere above Western Europe, whereas unfiltered nighttime ozone observations at the high Alpine sites are impacted by the European boundary layer and therefore do not reflect the ozone trend in the lower free troposphere of Western Europe. The Alpine sites of Zugspitze, Jungfraujoch and Sonnblick have provided important ozone observations from the center of Western Europe since 1978, and the trends have been analyzed to gain insight into the changes of baseline ozone that flows into Europe [Zanis et al., 1999; Oltmans et al., 2006; 2013; Gilge et al., 2010; Cui et al., 2011; Logan et al., 2012; Parrish et al., 2012; Cooper et al., 2014; Gaudel et al., 2018]. Because these sites are located 2800–3600 m above sea level, some past studies have considered these sites to be representative of the lower free-troposphere. However, many studies of trace gas and particulate matter observations at these and other Alpine sites, in conjunction with regional-scale transport analyses, have clearly shown that Alpine peaks are frequently impacted by emissions from the European boundary layer, especially in the summer months [Baltensperger et al., 1997; Carnuth et al., 2002; Zellweger et al., 2003; Henne et al., 2004; Steinbacher et al., 2004; Henne et al., 2005; Kaiser et al., 2007; Folini et al., 2009; Zellweger et al., 2009; Henne et al., 2010; Griffiths et al., 2014; Collaud Coen et al., 2018; Yuan et al., 2019a]. Previous work has questioned the reliability of the Jungfraujoch observations prior to 1994 [Zanis et al., 1999; Logan et al., 2012], however the remainder of this analysis focuses on data since 1994.
The Alpine sites are not truly remote because they are located in the center of Europe. However, local influences can be avoided by limiting the trend analysis to nighttime observations, which excludes the daytime upslope winds that transport air from the valleys up to the summits. The nighttime air masses may contain residual air from the previous day’s boundary layer if the boundary layer exceeded the elevation of the mountaintop, as demonstrated at North American sites like Mt. Bachelor, Oregon (2.8 km above sea level) [Weiss-Penzias et al., 2006] and Whistler, British Columbia (2.2 km above sea level) [Gallagher et al., 2012]. Influence from the European boundary layer at the Alpine summits is most common in the warm months, as determined from an analysis of the boundary layer tracer, radon, which has elevated levels at Jungfraujoch during the months of April–September [Griffiths et al., 2014]. Similarly, studies have documented the growth of the Alpine boundary layer to more than 1 km above the summit of Zugspitze [Carnuth et al., 2002], and a weekly cycle of CO2 at the summit of Zugspitze, caused by regional scale emissions [Yuan et al., 2019a, b]. Moist Alpine boundary layer air has also been observed in the lower free troposphere above Milan, Italy, after vertical transport by mountain venting processes and subsequent advection from the Alps to Milan [Henne et al., 2005].
In contrast to the high Alpine sites, the IAGOS observations at 650 hPa are above the European boundary layer [Petetin et al., 2016], as described in Section 2.3.8. This difference is illustrated by Figure 6 which compares monthly values of observed specific humidity (based on a 1995–2014 climatology) at the summit of Jungfraujoch to specific humidity at 650 hPa above Western Europe, as reported by IAGOS commercial aircraft (at the same altitude as Jungfraujoch). Nighttime specific humidity values are greater at Jungfraujoch during all months, indicating a greater influence from the moist boundary layer at Jungfraujoch, with an even larger difference for daytime conditions. The enhancement is greatest during the warm months, matching the Jungfraujoch radon analysis by Griffiths et al. . Comparison of European boundary layer specific humidity values to the values at 650 hPa and at Jungfraujoch (see Section 2.3.8) indicates that approximately 18% of the air at Jungfraujoch is from the boundary layer during the daytime or nighttime hours of winter (December-February), increasing to 33% during the night and 45% during the day in the summer months (June–August). This measurement-based analysis demonstrates that the Alpine observations are not fully representative of the lower free-tropospheric air masses observed by the IAGOS aircraft, especially in summer.
Figure 7 shows ozone trends above Western Europe (1994–2017) as measured by IAGOS aircraft on 10 pressure levels from the lower troposphere to the upper troposphere. The monthly means of ambient ozone are shown to illustrate the pronounced seasonal cycle of ozone that occurs above Western Europe, with a strong peak in summer at all levels (the data were filtered according to potential vorticity to remove stratospheric observations from the highest levels). Based on monthly anomalies, ozone increased in the mid- and upper troposphere (600–250 hPa) at the rate of 1.3 to 4.5 ppbv decade–1 (p-values less than 0.05), consistent with ozone increases above Germany and Belgium as observed by ozonesondes [Oltmans et al., 2013; Van Malderen et al., 2016]; trends in the lower troposphere (950–700 hPa) are also positive, but weaker (1.0–1.2 ppbv decade–1; p-values less than 0.05). The trend at 650 hPa, at the same altitude as Jungfraujoch, is 1.3 ppbv decade–1 (p = 0.00) (Table 2), which is similar to the trends in the mid-tropospheric layers above.
Figure 8 directly compares the IAGOS trend at 650 hPa to the trends at the three Alpine sites since 1995, plus the trends at three low-elevation rural sites in southern Germany, which are indicative of the polluted European boundary layer (see also Table S-1). IAGOS is the only time series with a clear positive trend, whereas ozone at Jungfraujoch is relatively unchanged since 1995, and ozone has decreased at Sonnblick, Zugspitze and the three low-elevation sites. These trends are based on data from all months of the year, and as shown next, the difference between IAGOS and the Alpine sites is driven by the summer months.
Figure 9 shows the ozone anomaly trends at the same sites as in Figure 8, but for the warm months of May–August when the European boundary layer is deep, and for the cold months of November–February when the boundary layer is shallow. During the cold months differences among the sites are small. IAGOS and Jungfraujoch show small positive trends, while ozone is flat at Zugspitze and Sonnblick, similar to the low-elevation sites. However, there is a greater difference between IAGOS and the other sites during the warm months. Ozone has decreased since 1995 at the three low-elevation sites, consistent with widespread summertime ozone decreases observed across much of Europe, as illustrated by the TOAR analysis in Supplemental Figure S-5. The low-elevation sites show the high surface ozone anomalies that occurred across Europe during the heatwave of August, 2003 [Vautard et al., 2005]. The trends at the Alpine sites are similar and they also show the summertime peak in 2003. In contrast the IAGOS trend (above the boundary layer) is positive but weak (0.6 ppbv decade–1; p = 0.34), and it shows no peak during 2003 (although IAGOS observed strong ozone enhancements below 650 hPa during August, 2003 [Tressol et al., 2008]). Further analysis is provided in Supplemental Figure S-6, to determine if the trends of the high and low ozone extremes (5th and 95th percentiles) are similar between IAGOS and Jungfraujoch. During the warm months there are no clear similarities between the two sites, but during the cold months positive trends are strongest for the 5th percentiles (1.0 – 1.9 ppbv decade–1), at both sites.
In conclusion, the negative trends at Sonnblick and Zugspitze, based on data from all months (Figure 8), are driven by the summertime decreases (Figure 9), which are also seen at the low elevation sites in southern Germany. The relatively flat trend at the higher elevation site of Jungfraujoch is in between the positive IAGOS trend and the negative trends at Sonnblick and Zugspitze (Figure 8). This observation is consistent with the analysis of Collaud Coen et al. , who found less influence from the European boundary layer at Jungfraujoch than at Zugspitze or Sonnblick. While the IAGOS data provide the most straight-forward assessment of lower free-tropospheric ozone trends above Europe (1.3 ± 0.8 ppbv decade–1 since 1994), it is still feasible to filter the Alpine data to isolate observations made in the free troposphere using co-located observations of trace gases and particulate matter [Zellweger et al., 2003; Yuan et al., 2018]. As a basic illustration, we used specific humidity observations at Jungfraujoch to isolate the low humidity air samples, which should be biased towards free tropospheric conditions. We found that during the warm months, the trend at Jungfraujoch approaches that of IAGOS when the sampling is restricted to low humidity air samples (Table S-2).
The goal of this analysis has been to examine long-term ozone trends at as many remote surface sites as possible, for the purposes of understanding multi-decadal regional-scale changes of surface ozone and for the evaluation of global atmospheric chemistry models [Young et al., 2018]. However, because these 27 sites only cover a relatively small portion of the globe, they do not provide a comprehensive overview of global surface ozone trends. Current research is attempting to quantify the extent to which the global ozone monitoring network represents the global ozone distribution at the surface and in the free troposphere [Sofen et al., 2016; Brown-Steiner et al., 2018; Chang et al., 2019; Young et al., 2018]. Sofen et al.  gathered present-day ozone observations from approximately 2400 regionally-representative monitoring sites worldwide, including most of the sites from the present analysis. Using a global atmospheric chemistry model they determined that these sites are representative of 25% of the Earth’s surface area (33% in the Northern Hemisphere and 18% in the Southern Hemisphere). The coverage was limited despite the large number of sites because most sites were clustered in North America, Europe and Japan. Therefore, we conclude that the trends reported by the present analysis are representative of far less than 25% of the Earth’s surface.
To place the 27 remote sites in the context of the global ozone monitoring network, Figure 10 shows the global distribution of observed surface ozone using all available monitoring sites (approximately 5000) from the TOAR Surface Ozone Database, below 2000 m elevation, and averaged onto a 2° × 2° grid for the period 2005–2014 [Schultz et al., 2017]. These data were retrieved from the TOAR archive (https://doi.pangaea.de/10.1594/PANGAEA.876108), which contains many observation-based data products (data through 2014) to facilitate research on regional and global ozone distributions. The ozone metric shown in Figure 10 is the monthly mean of the maximum daily 8-hour average, selected because the majority of these sites (urban, suburban and rural) experience diurnal cycles [Strode et al., 2018], and this metric avoids the nighttime and early morning hours when surface ozone is at a minimum due to surface deposition under stable conditions. The value shown for each grid cell is the annual maximum of the 12 monthly values to reveal the time of year and the ozone values associated with peak photochemical ozone production, which is strongest in low and mid-latitudes (plots of standard seasonal ozone values from the TOAR database are provided by Schultz et al.  and Gaudel et al. ). In terms of the seasonal ozone peak, the greatest ozone values are found from April to August at northern mid-latitudes (25°–45° N), primarily in the southwestern USA, the Mediterranean region, northern India, eastern China, South Korea and Japan. Ozone values are much less in the tropics and southern mid-latitudes. Similar results are found when the data are limited to just the rural sites (Figure S-7). With respect to latitude, peak ozone levels occur between 20°–50° N, the same zone with the greatest diversity of ozone trends seen at our remote sites (Figure 5) and in the polluted boundary layer of North America, Europe and East Asia (Figure S-5; Chang et al., 2017), consistent with the expectation that photochemical ozone production is most active in this region and is responding to changing precursor emissions [Zhang et al., 2016; Ziemke et al., 2019].
Focusing on the variable ozone trends at northern mid-latitudes, one might conclude that overall, ozone decreases are more common than increases since 1995 (Figure 5). But as discussed above, the number of available sites is too small to construct an area-weighted trend that is representative of the entire latitude band. An obvious shortcoming of this analysis is the lack of long-term rural monitoring sites across South and East Asia where ozone increases are expected due to increasing ozone precursor emissions [Zhang et al., 2016; Lin et al., 2017; Ziemke et al., 2019]. Relying on the peer-reviewed literature and the TOAR surface ozone database (with data through 2014), Gaudel et al.  concluded that surface and lower tropospheric ozone has generally increased across East Asia over the past two decades. This conclusion is reinforced by a new study that has provided the first overview of China’s extensive surface ozone monitoring network (1600 non-rural sites) for the period 2013–2017 [Lu et al., 2018]. Over this short 5-year period the data show a broad increase of ozone across the country. An update to this trend spanning the years 2013–2018 is provided in Supplemental Figure S-8, showing that ozone was similarly high in 2018. Our analysis also lacks long-term rural ozone monitoring at the west coast of North America, which would indicate the impact of rising Asian ozone on the eastern side of the North Pacific Ocean. Focusing on annual average baseline ozone observations, Jaffe et al.  found ozone increases at the summit of Mt Bachelor, Oregon (2763 m above sea level), from 2004 to 2016, but decreases over the same period at the marine boundary layer site of Trinidad Head on the northern California coast, located 850 km to the southwest of Mt. Bachelor (neither site has data prior to 2004). The opposing ozone trends at these baseline monitoring sites in the same region of the western USA illustrate the variable nature of ozone trends at northern mid-latitudes.
In terms of its contribution to radiative forcing, ozone in the free troposphere has a greater impact than ozone at the surface [Lacis et al., 1990; Forster and Shine, 1997; Worden et al., 2008, 2011; Bowman et al., 2013; Kuai et al., 2017]. Supplemental Table S-3 summarizes recent studies that have quantified trends of free tropospheric ozone and tropospheric column ozone at multiple locations around the world based on ozonesondes and IAGOS commercial aircraft observations [Oltmans et al., 2013; Cooper et al., 2014; Tarasick et al., 2016; Van Malderen et al., 2016; Cohen et al., 2018; Gaudel et al., 2018], and serves as an update to a similar table that appeared in the Fifth Assessment Report of the Intergovernmental Panel on Climate Change [IPCC, 2013; see Table 2.SM.1 in Hartmann et al., 2013]. Focusing on time series at least 20-years in length, Table S-3 demonstrates a general increase of ozone in the free troposphere of both hemispheres, although a few regions show no increase, or even a decrease in a few isolated layers of the troposphere. For the longest time series (>30 years) the trends can vary across shorter time periods, depending on the decades chosen for analysis [Oltmans et al., 2013; Tarasick et al., 2016]. These findings are consistent with the earlier assessment by IPCC [IPCC, 2013]. The ozone increases are especially prevalent across the northern tropics and mid-latitudes, with the strongest increases above South and East Asia in the range 2–6 ppbv decade–1, which are generally far greater than trends at the remote surface sites (Table 2). Clearly, the highly variable positive and negative trends at the surface, as shown in Figure 5, are not indicative of ozone trends in the free troposphere, which are overwhelmingly positive. This comparison is a further demonstration that scattered surface ozone trends cannot be assumed to be representative of ozone trends in other regions and levels of the troposphere.
While the TOAR database reveals the observation-based surface ozone distribution from all available monitoring sites (see Figure 10, and Gaudel et al. ), very large data gaps exist and models must be used for a complete global picture. The surface ozone distribution from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP) multi-model ensemble generally captures the same ozone peaks as the TOAR observations but with a high bias [Young et al., 2013a, 2013b, 2018]. The ACCMIP ensemble also indicates that the northern mid-latitude ozone enhancement (Figure 10) circles the globe, and is present in regions without ozone observations. Comparison to model simulations of pre-industrial ozone indicates that the northern mid-latitude ozone enhancement is due to anthropogenic emissions [Young et al. 2013a, 2013b]. Over time, the region of the Northern Hemisphere with the greatest net ozone production due to anthropogenic emissions has migrated southward as emissions have shifted from North America and Europe to Asia. A model study determined that emissions changes (in terms of magnitude and location) increased lower tropospheric ozone in the 10°–30° N latitude band by 3–5 ppb over the period 1980–2010 [Zhang et al., 2016]. This modeled rate of increase (1.0–1.7 ppbv decade–1) is similar to the observed rates at MLO and Izaña (Table 2). No other long-term remote monitoring sites are available from high elevations in the 10°–30° N latitude band, however additional support is provided by IAGOS commercial aircraft profiles, which revealed lower tropospheric ozone increases above southern India and Southeast Asia from the period 1994–2004 to 2005–2014 [Gaudel et al., 2018]. Furthermore, the Hok Tsui coastal site just south of Hong Kong has measured ozone in this very polluted region of southern China since 1994. The data have been filtered by Wang et al. [2009; 2019] to focus on marine air masses from the South China Sea, revealing a strong ozone increase of 3.6 ppbv decade–1.
Finally, we show how newly available ozone observations (since 2010) have updated our understanding of ozone variability at the three high elevation Alpine sites. Previous analysis of long-term ozone trends at these sites concluded that ozone increased throughout the 1990s, peaked in the early 2000s and then decreased until the time series ended in 2009–2011 [Parrish et al., 2012, 2014]. The rates of decrease were strongest in summer and were determined with quadratic fits. Our analysis, based on the lowess smoother, also shows ozone maxima in the late 1990s or early 2000s, followed by decreasing ozone until approximately 2010 (see time series plots in Appendix S-B in the Supplemental Material). However, the newly available data through 2016–2018 show that ozone has remained approximately level at the three Alpine sites since 2010, with a slight increase since 2015 at Jungfraujoch. When focusing on just the summer months, ozone in recent years is consistent with the overall decreasing trends observed at these sites since the late 1990s or early 2000s (Section 3.3 and Table S-1). In contrast, ozone in the other seasons has remained level or increased slightly (e.g Jungfraujoch in winter, Table S-1), resulting in annually averaged ozone levels that have changed little since 2010. Extension of these time series with future observations, and application of the lowess smoother to the new data, can quickly reveal if the near-level ozone values of recent years will continue.
This study has estimated surface ozone trends at 27 globally distributed remote locations (20 in the Northern Hemisphere, and 7 in the Southern Hemisphere), focusing on continuous ozone time series that extend from the present back to at least 1995. The analysis builds on the original TOAR effort by providing multi-decadal trend analysis at 22 remote sites that were not explored by Gaudel et al. . To avoid the confounding influence of ozone’s seasonal cycle and periods of missing data, the trends are based on monthly mean ozone anomalies rather than ambient ozone mixing ratios, using a statistical method that was not employed by TOAR [Gaudel et al., 2018]. Since 1995, ozone trends at the available Northern Hemisphere sites are nearly evenly split between positive and negative trends, with more than half of the trends being relatively weak, between 1 and –1 ppbv decade–1 (p-values typically greater than 0.10); the Southern Hemisphere had positive trends at 5 out of 7 sites. In both hemispheres, the robust positive trends (p-values less than 0.10) are in the range of 0.5–2 ppbv decade–1. The longest time series available are from South Pole, where ozone is essentially unchanged since the early 1960s, and Mauna Loa, Hawaii where ozone has increased by roughly 50% since the late 1950s (~2.3 ppbv decade–1).
Particular focus was placed on the high elevation Alpine monitoring sites, which were compared to IAGOS commercial aircraft observations in the lower free-troposphere above Western Europe. The Alpine sites are frequently impacted by the polluted European boundary layer, especially in summer, and can only be used to quantify lower free tropospheric ozone if the time series are carefully filtered to avoid observations impacted by the boundary layer. In contrast, the IAGOS observations at 650 hPa are above the European boundary layer, and show that ozone in the lower free troposphere above Western Europe has increased at the rate of 1.3 ± 0.8 ppbv decade–1 since 1994. Stronger increases were detected in the mid- and upper troposphere (1.5–4.5 ppbv decade–1).
We emphasize that while we used all long-term remote monitoring sites available, the data are only representative of much less than 25% of the global surface area, and therefore they cannot be used to produce a global mean surface ozone trend. Full understanding of global surface ozone trends based on observations would require a major expansion of the surface ozone observation network. Based on newly developed methods [Sofen et al., 2016; Weatherhead et al., 2017; Chang et al., 2019] the locations of these additional sites could be carefully planned to maximize their spatial representativeness.
We conducted a review of the recent peer-reviewed literature to summarize free tropospheric (primarily in the range 700–300 hPa) and tropospheric column ozone trends around the world, beginning in 1995 or earlier (Table S-3). The results revealed a general increase of ozone in the free troposphere of both hemispheres, although a few sites showed no increase, or even a decrease in a few isolated layers of the troposphere, and the trends can vary depending on the time period chosen for analysis. Since the mid-1990s free tropospheric ozone increases are especially prevalent across the northern tropics and mid-latitudes, with the strongest increases above South and East Asia in the range 2–6 ppbv decade–1, which are generally far greater than trends at the remote surface sites, either at sea level or on mountaintops. We conclude that the highly variable positive and negative trends at the surface are not necessarily indicative of ozone trends in the free troposphere, which have been overwhelmingly positive since the mid-1990s.
The ozone time series presented in this analysis provide an important benchmark for the evaluation of multi-decadal chemistry-climate model simulations of tropospheric ozone. We recommend that these remote sites constitute one component of a three-step approach:
Care is required when selecting the appropriate model grid cell and vertical layer for comparison to these remote surface sites. For example, the Cape Point data were filtered for onshore flow conditions when transport is from the west and south. Therefore to focus on conditions above the South Atlantic Ocean a model grid cell should be chosen that is to the west of Cape Town where recent continental outflow is infrequent. For a mountaintop site, such as Jungfraujoch, the actual elevation of the station will likely be far above the coarse model terrain, and therefore a grid cell should be chosen that does not reside in the free troposphere above the Alpine boundary layer. However, this complication does not arise for Mauna Loa because the terrain of Hawaii is not resolved by a coarse-resolution global-scale model. Therefore, a direct comparison can be made between the nighttime ozone observations at Mauna Loa (representative of the lower free troposphere) and a free tropospheric model grid cell at the same elevation. Selection of the most appropriate grid cell for model evaluation will vary by model. We recommend that a range of grid cells surrounding the sampling coordinates be examined, in order to identify the cell that most closely matches the sampling environment of the remote monitoring site.
Once the appropriate model time series has been selected for evaluation against the observed ozone time series, we recommend the following straightforward statistical analysis to determine if the modeled long-term ozone trend, bias and interannual variability are consistent with the observed values.
The field of climate change research has developed a range of widely accepted statistical methods for the analysis of trends, extreme events and model evaluation [von Storch and Zwiers, 1999; Zwiers and von Storch, 2004; Hennemuth et al., 2013], as well as common practices for communicating uncertainty in assessment findings [Mastrandrea et al., 2011]. Statistical analysis in the field of atmospheric chemistry has not yet reached this level of maturity. Development of a suite of best statistical practices for atmospheric chemistry would be of great value to the field, and is an endeavor that could be effectively addressed by the next phase of the Tropospheric Ozone Assessment Report (https://igacproject.org/activities/TOAR/TOAR-II).
The surface ozone observations reported in this paper, from 1970 to the present, can be downloaded from the TOAR Surface Ozone Database via the JOIN web interface: https://join.fz-juelich.de. The historical ozone observations from MLO (1957–1959) and SPO (1961–1963) are available from NOAA’s Global Monitoring Laboratory: ftp://aftp.cmdl.noaa.gov/data/ozwv/SurfaceOzone/Historical/. IAGOS aircraft observations are available from: https://doi.org/10.25326/20.
In addition, the monthly surface ozone values upon which the trends were calculated can be easily downloaded as ASCII text files from the following URL: http://doi.org/10.34730/e792cad833174ebcafd9f052711e5660.
The supplemental file for this article can be found as follows:
We thank Forschungszentrum Jülich for funding of the TOAR database development and its maintenance. Many of the times series in this analysis were obtained from the EBAS database, which is largely funded by the UN-ECE CLRTAP (EMEP), AMAP and through Norwegian Institute for Air Research (NILU) internal resources. Specific developments have been possible due to projects like EUSAAR (EU-FP5), EBAS-Online (Norwegian Research Council INFRA) and HTAP (European Commission DG-ENV). A large number of specific projects have supported development of data and meta data reporting schemes in dialog with EBAS data providers. The IAGOS program acknowledges the European Commission for its support of the MOZAIC project (1994–2003) the preparatory phase of IAGOS (2005–2013) and IGAS (2013–2016); the partner institutions of the IAGOS Research Infrastructure (FZJ, DLR, MPI, KIT in Germany, CNRS, Météo-France, Université Paul Sabatier in France, and University of Manchester, UK); the French Atmospheric Data Center AERIS for hosting the database; and the participating airlines (Lufthansa, Air France, China Airlines, Iberia, Cathay Pacific, Hawaiian Airlines) for transporting the instrumentation free of charge. Special thanks also goes to the following scientists, air quality specialists and agencies for providing ozone data from the remote and rural monitoring sites: Weili Lin, Meteorological Observation Center, China Meteorological Administration, Beijing, for the Mt. Waliguan data; Rolf Weller, Alfred Wegener Institute, Germany, for the Neumayer, Antarctica data; Mr. Kazuyuki Saito (firstname.lastname@example.org), Japan Meteorological Agency (JMA) for the Minamitorishima GAW global station data; Gary Lear, U.S. Environmental Protection Agency Clean Air Markets Division Clean Air Status and Trends Network (CASTNET), for the data from Denali, Gothic, Great Basin, Grand Canyon and Centennial; Ute Dauert and Stefan Feigenspahn, Umweltbundesamt Dessau, Germany for obtaining the ozone measurements from the German federal air quality network; Thumeka Mkololo, South African Weather Service, for providing the baseline filtered ozone data at Cape Point; Gastón Torres Aravena, Dirección Meteorológica de Chile, for providing the data from El Tololo, Chile; Iris Buxbaum, Umweltbundesamt/Federal Environment Agency, Austria, for providing the Sonnblick data; Landesamt für Umwelt, Wasserwirtschaft und Gewerbeaufsicht, Rheinland Pfalz provided the Pfälzerwald-Hortenkopf measurements; Landesanstalt für Umwelt, Messungen und Naturschutz, Baden-Württemberg provided the Schwarzwald-Süd measurements; the Scottish Environment Protection Agency provided the Strath Vaich Dam data. Martin Steinbacher acknowledges funding from the GAW Quality Assurance/Science Activity Centre Switzerland (QA/SAC-CH), which is supported by MeteoSwiss and Empa.
The authors have no competing interests to declare.
Adame, JA, Cupeiro, M, Yela, M, Cuevas, E and Carbajal, G. 2019. Ozone and carbon monoxide at the Ushuaia GAW-WMO global station. Atmospheric Research 217: 1–9. DOI: 10.1016/j.atmosres.2018.10.015
Anet, JG, Steinbacher, M, Gallardo, L, Velásquez Álvarez, PA, Emmenegger, L and Buchmann, B. 2017. Surface ozone in the Southern Hemisphere: 20 years of data from a site with a unique setting in El Tololo, Chile. Atmos. Chem. Phys ., 17: 6477–6492. DOI: 10.5194/acp-17-6477-2017
Baltensperger, U, Gäggeler, HW, Jost, DT, Lugauer, M, Schwikowski, M, Weingartner, E and Seibert, P. 1997. Aerosol climatology at the high-alpine site Jungfraujoch, Switzerland. J. Geophys. Res ., 102(D16): 19707–19715. DOI: 10.1029/97JD00928
Banerjee, A, Fyfe, JC, Polvani, LM, Waugh, D and Chang, K-L. 2020. A pause in Southern Hemisphere circulation trends due to the Montreal Protocol. Nature 579: 544–548. DOI: 10.1038/s41586-020-2120-4
Barnes, EA, Fiore, AM and Horowitz, LW. 2016. Detection of trends in surface ozone in the presence of climate variability. J. Geophys. Res. Atmos ., 121: 6112–6129. DOI: 10.1002/2015JD024397
Blunden, J, Arndt, DS and Hartfield, G. (eds.). 2018. State of the Climate in 2017. Bull. Amer. Meteor. Soc ., 99(8): Si–S332. DOI: 10.1175/2018BAMSStateoftheClimate.1
Bowen, IG and Regener, VH. 1951. On the automatic chemical determination of atmospheric ozone. Journal of Geophysical Research 56(3): 307–324. DOI: 10.1029/JZ056i003p00307
Bowman, KW, Shindell, DT, Worden, HM, Lamarque, JF, Young, PJ, Stevenson, DS, Qu, Z, de la Torre, M, Bergmann, D, Cameron-Smith, PJ and Collins, WJ. 2013. Evaluation of ACCMIP outgoing longwave radiation from tropospheric ozone using TES satellite observations. Atmos. Chem. Phys ., 13: 4057–4072. DOI: 10.5194/acp-13-4057-2013
Box, GE, Jenkins, GM, Reinsel, GC and Ljung, GM. 2015. Time series analysis: forecasting and control (5th ed.). John Wiley & Sons.
Brown-Steiner, B, Selin, NE, Prinn, RG, Monier, E, Tilmes, S, Emmons, L and Garcia-Menendez, F. 2018. Maximizing ozone signals among chemical, meteorological, and climatological variability. Atmos. Chem. Phys ., 18: 8373–8388. DOI: 10.5194/acp-18-8373-2018
Brunke, EG, Labuschagne, C, Parker, B, Scheel, HE and Whittlestone, S. 2004. Baseline air mass selection at Cape Point, South Africa: application of 222Rn and other filter criteria to CO2. Atmospheric Environment 38(33): 5693–5702. DOI: 10.1016/j.atmosenv.2004.04.024
Buchmann, B, Klausen, J and Zellweger, C. 2009. Traceability of Long-Term Atmospheric Composition Observations across Global Monitoring Networks: Chemical Metrology Applied to the Measurements of Constituents in Air, Water, and Soil. CHIMIA International Journal for Chemistry , Volume 63, Number 10, Month: October 2009, 657–660(4). DOI: 10.2533/chimia.2009.657
Carnuth, W, Kempfer, U and Trickl, T. 2002. Highlights of the tropospheric lidar studies at IFU within the TOR project. Tellus B: Chemical and Physical Meteorology 54(2): 163–185. DOI: 10.3402/tellusb.v54i2.16656
Chandler, R and Scott, M. 2011. Statistical Methods for Trend Detection and Analysis in the Environmental Sciences , 368. John Wiley & Sons. DOI: 10.1002/9781119991571
Chang, K-L, Cooper, OR, West, JJ, Serre, ML, Schultz, MG, Lin, M, Marécal, V, Josse, B, Deushi, M, Sudo, K, Liu, J and Keller, CA. 2019. A new method (M3Fusion v1) for combining observations and multiple model output for an improved estimate of the global surface ozone distribution. Geosci. Model Dev ., 12: 955–978. DOI: 10.5194/gmd-12-955-2019
Chang, K-L, Petropavlovskikh, I, Cooper, OR, Schultz, MG and Wang, T. 2017. Regional trend analysis of surface ozone observations from monitoring networks in eastern North America, Europe and East Asia. Elem Sci Anth ., 5: 50. DOI: 10.1525/elementa.243
Cleveland, WS. 1979. Robust locally weighted regression and smoothing scatterplots. Journal of the American statistical association 74(368): 829–836. DOI: 10.1080/01621459.1979.10481038
Cleveland, WS and Devlin, SJ. 1988. Locally weighted regression: an approach to regression analysis by local fitting. Journal of the American Statistical Association 83(403): 596–610. DOI: 10.1080/01621459.1988.10478639
Cochrane, D and Orcutt, GH. 1949. Application of least squares regression to relationships containing auto-correlated error terms. Journal of the American Statistical Association 44(245): 32–61. DOI: 10.2307/2280349
Cohen, Y, Petetin, H, Thouret, V, Marécal, V, Josse, B, Clark, H, Sauvage, B, Fontaine, A, Athier, G, Blot, R, Boulanger, D, Cousin, J-M and Nédélec, P. 2018. Climatology and long-term evolution of ozone and carbon monoxide in the UTLS at northern mid-latitudes, as seen by IAGOS from 1995 to 2013. Atmos. Chem. Phys ., 18: 5415–5453. DOI: 10.5194/acp-18-5415-2018
Collaud Coen, M, Andrews, E, Aliaga, D, Andrade, M, Angelov, H, Bukowiecki, N, Ealo, M, Fialho, P, Flentje, H, Hallar, AG, Hooda, R, Kalapov, I, Krejci, R, Lin, N-H, Marinoni, A, Ming, J, Nguyen, NA, Pandolfi, M, Pont, V, Ries, L, Rodríguez, S, Schauer, G, Sellegri, K, Sharma, S, Sun, J, Tunved, P, Velasquez, P and Ruffieux, D. 2018. Identification of topographic features influencing aerosol observations at high altitude stations. Atmos. Chem. Phys ., 18: 12289–12313. DOI: 10.5194/acp-18-12289-2018
Collins, WJ, Lamarque, J-F, Schulz, M, Boucher, O, Eyring, V, Hegglin, MI, Maycock, A, Myhre, G, Prather, M, Shindell, D and Smith, SJ. 2017. AerChemMIP: quantifying the effects of chemistry and aerosols in CMIP6. Geosci. Model Dev ., 10: 585–607. DOI: 10.5194/gmd-10-585-2017
Cooper, OR, Gao, R-S, Tarasick, D, Leblanc, T and Sweeney, C. 2012. Long-term ozone trends at rural ozone monitoring sites across the United States, 1990–2010. J. Geophys. Res ., 117: D22307. DOI: 10.1029/2012JD018261
Cooper, OR, Parrish, DD, Ziemke, J, Balashov, NV, Cupeiro, M, Galbally, IE, Gilge, S, Horowitz, L, Jensen, NR, Lamarque, J-F, Naik, V, Oltmans, SJ, Schwab, J, Shindell, DT, Thompson, AM, Thouret, V, Wang, Y and Zbinden, RM. 2014. Global distribution and trends of tropospheric ozone: An observation-based review. Elem Sci Anth 2: 29. DOI: 10.12952/journal.elementa.000029
Cristofanelli, P, di Carlo, P, Salisburgo, CD, Tuccella, P, Biancofiore, F, Stocchi, P, Verza, GP, Landi, TC, Marinoni, A, Calzolari, F and Duchi, R. 2013. Analysis of Summer Ozone Observations at a High Mountain Site in Central Italy (Campo Imperatore, 2388 m a.s.l.). Pure Appl. Geophys ., 170: 1985–1999. DOI: 10.1080/01621459.1988.10478639
Cuevas, E, Gómez-Peláez, AJ, Rodríguez, S, Terradellas, E, Basart, S, García, RD, García, OE and Alonso-Pérez, S. 2017. The pulsating nature of large-scale Saharan dust transport as a result of interplays between mid-latitude Rossby waves and the North African Dipole Intensity. Atmospheric Environment 167: 586–602. ISSN 1352-2310. DOI: 10.1016/j.atmosenv.2017.08.059
Cuevas, E, González, Y, Rodríguez, S, Guerra, JC, Gómez-Peláez, AJ, Alonso-Pérez, S, Bustos, J and Milford, C. 2013. Assessment of atmospheric processes driving ozone variations in the subtropical North Atlantic free troposphere. Atmos. Chem. Phys 13: 1973–1998. DOI: 10.5194/acp-13-1973-2013
Cui, J, Pandey Deolal, S, Sprenger, M, Henne, S, Staehelin, J, Steinbacher, M and Nédélec, P. 2011. Free tropospheric ozone changes over Europe as observed at Jungfraujoch (1990–2008): An analysis based on backward trajectories. J. Geophys. Res ., 116. D10304. DOI: 10.1029/2010JD015154
Derek, N, Krummel, P and Cleland, S. (eds.). 2016. Baseline: History and Recollections – 40th Anniversary Special Edition. Melbourne, Australia: CSIRO Oceans and Atmosphere and Bureau of Meteorology. http://www.bom.gov.au/inside/cgbaps/baseline/Baseline_40_Anniv_special_edition.pdf.
Derwent, RG, Manning, AJ, Simmonds, PG, Spain, TG and O’Doherty, S. 2018. Long-term trends in ozone in baseline and European regionally-polluted air at Mace Head, Ireland over a 30-year period. Atmos. Environ ., 179: 279–287. DOI: 10.1016/j.atmosenv.2018.02.024
Derwent, RG, Simmonds, PG, Manning, AJ and Spain, TG. 2007. Trends over a 20-year period from 1987 to 2007 in surface ozone at the atmospheric research station, Mace Head, Ireland. Atmospheric Environment 41(39): 9091–9098. DOI: 10.1016/j.atmosenv.2007.08.008
Escudero, M, Lozano, A, Hierro, J, Valle, JD and Mantilla, E. 2014. Urban influence on increasing ozone concentrations in a characteristic Mediterranean agglomeration. Atmos. Environ ., 99: 322–332. DOI: 10.1016/j.atmosenv.2014.09.061
Fischer, EV, Jaffe, DA and Weatherhead, EC. 2011. Free tropospheric peroxyacetyl nitrate (PAN) and ozone at Mount Bachelor: Potential causes of variability and timescale for trend detection. Atmospheric Chemistry and Physics 11: 5641–5654. DOI: 10.5194/acp-11-5641-2011
Fleming, ZL, Doherty, RM, von Schneidemesser, E, Malley, CS, Cooper, OR, Pinto, JP, Colette, A, Xu, X, Simpson, D, Schultz, MG, Lefohn, AS, Hamad, S, Moolla, R, Solberg, S and Feng, Z. 2018. Tropospheric Ozone Assessment Report: Present-day ozone distribution and trends relevant to human health. Elem Sci Anth ., 6(1): 12. DOI: 10.1525/elementa.273
Folini, D, Kaufmann, P, Ubl, S and Henne, S. 2009. Region of influence of 13 remote European measurement sites based on modeled carbon monoxide mixing ratios. J. Geophys. Res ., 114: D08307. DOI: 10.1029/2008JD011125
Fornberg, B and Zuev, J. 2007. The Runge phenomenon and spatially variable shape parameters in RBF interpolation. Computers & Mathematics with Applications 54(3): 379–398. DOI: 10.1016/j.camwa.2007.01.028
Forster, P and Shine, K. 1997. Radiative forcing and temperature trends from stratospheric ozone changes. J. Geophys. Res. Atmos ., 102: 10841–10855. DOI: 10.1029/96JD03510
Galbally, IE, Bentley, ST and Meyer, CP. 2000. Mid-latitude marine boundary-layer ozone destruction at visible sunrise observed at Cape Grim, Tasmania, 41°S. Geophysical Research Letters 27(23): 3841–3844. DOI: 10.1029/1999GL010943
Galbally, IE, Schultz, MG, Buchmann, B, Gilge, S, Guenther, F, Koide, H, Oltmans, S, Patrick, L, Scheel, H-E, Smit, H, Steinbacher, M, Steinbrecht, W, Tarasova, O, Viallon, J, Volz-Thomas, A, Weber, M, Wielgosz, R and Zellweger, C. 2013. Guidelines for Continuous Measurement of Ozone in the Troposphere, GAW Report No 209, Publication WMO-No. 1110, ISBN 978-92-63-11110-4, WMO, Geneva. http://www.wmo.int/pages/prog/arep/gaw/gaw-reports.html.
Gallagher, JP, McKendry, IG and Cottle, PW. 2012. Application of Lidar Data to Assist Airmass Discrimination at the Whistler Mountaintop Observatory. J. of Applied Meteorology and Climate 51: 1733–1739. DOI: 10.1175/JAMC-D-12-067.1
Gaudel, A, Cooper, OR, Ancellet, G, Barret, B, Boynard, A, Burrows, JP, Clerbaux, C, Coheur, PF, Cuesta, J, Cuevas, E, Doniki, S, Dufour, G, Ebojie, F, Foret, G, Garcia, O, Granados-Muñoz, MJ, Hannigan, JW, Hase, F, Hassler, B, Huang, G, Hurtmans, D, Jaffe, D, Jones, N, Kalabokas, P, Kerridge, B, Kulawik, S, Latter, B, Leblanc, T, Le Flochmoën, E, Lin, W, Liu, J, Liu, X, Mahieu, E, McClure-Begley, A, Neu, JL, Osman, M, Palm, M, Petetin, H, Petropavlovskikh, I, Querel, R, Rahpoe, N, Rozanov, A, Schultz, MG, Schwab, J, Siddans, R, Smale, D, Steinbacher, M, Tanimoto, H, Tarasick, DW, Thouret, V, Thompson, AM, Trickl, T, Weatherhead, E, Wespes, C, Worden, HM, Vigouroux, C, Xu, X, Zeng, G and Ziemke, J. 2018. Tropospheric Ozone Assessment Report: Present-day distribution and trends of tropospheric ozone relevant to climate and global atmospheric chemistry model evaluation. Elem. Sci. Anth ., 6(1): 39. DOI: 10.1525/elementa.291
Gheusi, F. 2011. Pic 2005, a field campaign to investigate low-tropospheric ozone variability in the Pyrenees. Atmospheric Research 101: 640–665. DOI: 10.1016/j.atmosres.2011.04.014
Gilge, S, Plass-Duelmer, C, Fricke, W, Kaiser, A, Ries, L, Buchmann, B and Steinbacher, M. 2010. Ozone, carbon monoxide and nitrogen oxides time series at four alpine GAW mountain stations in central. Europe, Atmos. Chem. Phys ., 10: 12295–12316. DOI: 10.5194/acp-10-12295-2010
Griffiths, AD, Conen, F, Weingartner, E, Zimmermann, L, Chambers, SD, Williams, AG and Steinbacher, M. 2014. Surface-to-mountaintop transport characterised by radon observations at the Jungfraujoch. Atmospheric Chemistry and Physics 14(23): 12763–12779. DOI: 10.5194/acp-14-12763-2014
Harris, JM and Kahl, JD. 1990. A descriptive atmospheric transport climatology for the Mauna Loa Observatory using clustered trajectories. J. Geophys. Res ., 95: 13651–13667. DOI: 10.1029/JD095iD09p13651
Hartmann, DL, Klein Tank, AMG, Rusticucci, M, Alexander, L, Brönnimann, S, Charabi, Y, Dentener, F, Dlugokencky, E, Easterling, D, Kaplan, A, Soden, B, Thorne, P, Wild, M and Zhai, PM. 2013. Observations: Atmosphere and Surface Supplementary Material. In: Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change . In: Stocker, TF, Qin, D, Plattner, G-K, Tignor, M, Allen, SK, Boschung, J, Nauels, A, Xia, Y, Bex, V and Midgley, PM (eds.). Available from www.climatechange2013.org and www.ipcc.ch.
He, J, Naik, V, Horowitz, LW, Dlugokencky, E and Thoning, K. 2020. Investigation of the global methane budget over 1980–2017 using GFDL-AM4.1. Atmos. Chem. Phys ., 20: 805–827. DOI: 10.5194/acp-20-805-2020
Helten, M, Smit, HGJ, Sträter, W, Kley, D, Nedelec, P, Zöger, M and Busen, R. 1998. Calibration and performance of automatic compact instrumentation for the measurement of relative humidity from passenger aircraft. J. Geophys. Res. Atmos ., 103(D19): 25643–25652. DOI: 10.1029/98JD00536
Henne, S, Brunner, D, Folini, D, Solberg, S, Klausen, J and Buchmann, B. 2010. Assessment of parameters describing representativeness of air quality in-situ measurement sites. Atmos. Chem. Phys ., 10: 3561–3581. DOI: 10.5194/acp-10-3561-2010
Henne, S, Furger, M, Nyeki, S, Steinbacher, M, Neininger, B, de Wekker, SFJ, Dommen, J, Spichtinger, N, Stohl, A and Prévôt, ASH. 2004. Quantification of topographic venting of boundary layer air to the free troposphere. Atmospheric Chemistry and Physics 4: 497–509. DOI: 10.5194/acp-4-497-2004
Henne, S, Furger, M and Prévôt, ASH. 2005. Climatology of Mountain Venting–Induced Elevated Moisture Layers in the Lee of the Alps. J. of Applied Meteorology , 44: 620–633. DOI: 10.1175/JAM2217.1
Hennemuth, B, Bender, S, Bülow, K, Dreier, N, Keup-Thiel, E, Krüger, O, Mudersbach, C, Radermacher, C and Schoetter, R. 2013. Statistical methods for the analysis of simulated and observed climate data: applied in projects and institutions dealing with climate change impact and adaptation, CSC Report 13, Climate Service Center, Germany.
Herzog, A, Buchmann, B and Hofer, P. 1996. System and performance audit for surface ozone – Global GAW station Zugspitze Germany, APRIL 1996. https://www.empa.ch/web/s503/wcc-empa.
Hoesly, RM, Smith, SJ, Feng, L, Klimont, Z, Janssens-Maenhout, G, Pitkanen, T, Seibert, JJ, Vu, L, Andres, RJ, Bolt, RM and Bond, TC. 2018. Historical (1750–2014) anthropogenic emissions of reactive gases and aerosols from the Community Emissions Data System (CEDS). Geoscientific Model Development 11(1): 369–408. DOI: 10.5194/gmd-11-369-2018
IPCC. 2013. Climate Change 2013: The Physical Science Basis. Contribution of Working Group I to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. In: Stocker, TF, Qin, D, Plattner, G-K, Tignor, M, Allen, SK, Boschung, J, Nauels, A, Xia, Y, Bex, V and Midgley, PM (eds.). 1535. Cambridge, United Kingdom and New York, NY, USA: Cambridge University Press.
Jaffe, DA, Cooper, OR, Fiore, AM, Henderson, BH, Tonneson, GS, Russell, AG, Henze, DK, Langford, AO, Lin, M and Moore, T. 2018. Scientific assessment of background ozone over the U.S.: Implications for air quality management. Elem. Sci. Anth ., 6(1): 56. DOI: 10.1525/elementa.309
Judd, CM, McClelland, GH and Ryan, CS. 2011. Data analysis: A model comparison approach. Routledge. DOI: 10.4324/9780203892053
Kaiser, A, Schelfinger, H, Spangl, W, Weiss, A, Gilge, S, Fricke, W, Ries, L, Cemas, D and Jesenovec, B. 2007. Transport of nitrogen oxides, carbon monoxide and ozone to the Alpine Global Atmosphere Watch stations Jungfraujoch (Switzerland), Zugspitze and Hohenpeissenberg (Germany), Sonnblick (Austria) and Mt. Krvavec (Slovenia). Atmos. Environ ., 41: 9273–9287. DOI: 10.1016/j.atmosenv.2007.09.027
Kentarchos, A, Roelofs, GJ, Lelieveld, J and Cuevas, E. 2000. On the origin of elevated surface ozone concentrations at Izana Observatory during the last days of March 1996: a model study. Geophys. Res. Lett ., 27(22): 3,699–3,702. DOI: 10.1029/2000GL011518
Klausen, J, Zellweger, C, Buchmann, B and Hofer, P. 2003. Uncertainty and bias of surface ozone measurements at selected Global Atmosphere Watch sites. J. Geophys. Res ., 108: 4622. DOI: 10.1029/2003JD003710
Krause, P, Boyle, DP and Bäse, F. 2005. Comparison of different efficiency criteria for hydrological model assessment. Adv. Geosci ., 5: 89–97. DOI: 10.5194/adgeo-5-89-2005
Kuai, L, Bowman, KW, Worden, HM, Herman, RL and Kulawik, SS. 2017. Hydrological controls on the tropospheric ozone greenhouse gas effect. Elem Sci Anth , 5: 10. DOI: 10.1525/elementa.208
Lacis, AA, Wuebbles, DJ and Logan, JA. 1990. Radiative forcing of climate by changes in the vertical distribution of ozone. J. Geophys. Res ., 95: 9971–9981. DOI: 10.1029/JD095iD07p09971
Lin, M, Horowitz, LW, Payton, R, Fiore, AM and Tonnesen, GS. 2017. US surface ozone trends and extremes from 1980 to 2014: quantifying the roles of rising Asian emissions, domestic controls, wildfires, and climate. Atmos. Chem. Phys ., 17: 2943–2970. DOI: 10.5194/acp-17-2943-2017
Lin, M, Fiore, AM, Horowitz, LW, Langford, AO, Oltmans, SJ, Tarasick, D and Rieder, HE. 2015. Climate variability modulates western US ozone air quality in spring via deep stratospheric intrusions. Nature communications 6: 7105. DOI: 10.1038/ncomms8105
Lin, M, Horowitz, LW, Oltmans, SJ, Fiore, AM and Fan, S. 2014. Tropospheric ozone trends at Mauna Loa Observatory tied to decadal climate variability. Nature Geoscience 7: 136–143 DOI: 10.1038/ngeo2066
Lin, MY, Malyshev, S, Shevliakova, E, Paulot, F, Horowitz, LW, Fares, S, Mikkelsen, TN and Zhang, L. 2019. Sensitivity of ozone dry deposition to ecosystem-atmosphere interactions: A critical appraisal of observations and simulations. Global Biogeochemical Cycles 33(10). DOI: 10.1029/2018GB006157
Liu, G, Liu, J, Tarasick, DW, Fioletov, VE, Jin, JJ, Moeini, O, Liu, X, Sioris, CE and Osman, M. 2013. A global tropospheric ozone climatology from trajectory-mapped ozone soundings. Atmos. Chem. Phys ., 13: 10659–10675. DOI: 10.5194/acp-13-10659-2013
Logan, JA. 1985. Tropospheric ozone: Seasonal behavior, trends, and anthropogenic influence. Journal of Geophysical Research: Atmospheres 90(D6): 10463–10482. DOI: 10.1029/JD090iD06p10463
Logan, JA. 1999a. An analysis of ozonesonde data for the troposphere: Recommendations for testing 3-D models, and development of a gridded climatology for tropospheric ozone. J. Geophys. Res ., 104: 16115–16149. DOI: 10.1029/1998JD100096
Logan, JA, Megretskaia, IA, Miller, AJ, Tiao, GC, Choi, D, Zhang, L, Stolarski, RS, Labow, GJ, Hollandsworth, SM, Bodeker, GE, Claude, H, De Muer, D, Kerr, JB, Tarasick, DW, Oltmans, SJ, Johnson, B, Schmidlin, F, Staehelin, J, Viatte, P and Uchino, O. 1999b. Trends in the vertical distribution of ozone: A comparison of two analyses of ozonesonde data. J. Geophys. Res ., 104: 26373–26399. DOI: 10.1029/1999JD900300
Logan, JA, Staehelin, J, Megretskaia, IA, Cammas, J-P, Thouret, V, Claude, H, De Backer, H, Steinbacher, M, Scheel, H-E, Stübi, R, Fröhlich, M and Derwent, R. 2012. Changes in ozone over Europe: Analysis of ozone measurements from sondes, regular aircraft (MOZAIC) and alpine surface sites. J. Geophys. Res ., 117: D09301. DOI: 10.1029/2011JD016952
Lu, X, Hong, J, Zhang, L, Cooper, OR, Schultz, MG, Xu, X, Wang, T, Gao, M, Zhao, Y and Zhang, Y. 2018. Severe surface ozone pollution in China: a global perspective. Environ. Sci. Technol. Lett . 5: 487–494. DOI: 10.1021/acs.estlett.8b00366
Lu, X, Zhang, L, Zhao, Y, Jacob, DJ, Hu, Y, Hu, L, Gao, M, Liu, X, Petropavlovskikh, I, McClure-Begley, A and Querel, R. 2019. Surface and tropospheric ozone trends in the Southern Hemisphere since 1990: possible linkages to poleward expansion of the Hadley Circulation. Science Bulletin 64: 400–409. DOI: 10.1016/j.scib.2018.12.021
Marenco, A, Thouret, V, Nédélec, P, Smit, H, Helten, M, Kley, D, Karcher, F, Simon, P, Law, K, Pyle, J and Poschmann, G. 1998. Measurement of ozone and water vapor by Airbus in-service aircraft: The MOZAIC airborne program, an overview. J. Geophys. Res ., 103(D19): 25631–25642. DOI: 10.1029/98JD00977
Mastrandrea, MD, Mach, KJ, Plattner, GK, Edenhofer, O, Stocker, TF, Field, CB, Ebi, KL and Matschoss, PR. 2011. The IPCC AR5 guidance note on consistent treatment of uncertainties: a common approach across the working groups. Climatic Change , 108(4): 675. DOI: 10.1007/s10584-011-0178-6
Mills, G, Pleijel, H, Malley, CS, Sinha, B, Cooper, OR, Schultz, MG, Neufeld, HS, Simpson, D, Sharps, K, Feng, Z, Gerosa, G, Harmens, H, Kobayashi, K, Saxena, P, Paoletti, E, Sinha, V and Xu, X. 2018. Tropospheric Ozone Assessment Report: Present-day tropospheric ozone distribution and trends relevant to vegetation, Elem. Sci. Anth ., 6(1): 47. DOI: 10.1525/elementa.302
Miyazaki, K, Eskes, H, Sudo, K, Boersma, KF, Bowman, K and Kanaya, Y. 2017. Decadal changes in global surface NOx emissions from multi-constituent satellite data assimilation. Atmos. Chem. Phys ., 17: 807–837. DOI: 10.5194/acp-17-807-2017
Molloy, SB and Galbally, IE. 2014. Analysis and identification of a suitable baseline definition for tropospheric ozone at Cape Grim, Tasmania, in Baseline Atmospheric Program (Australia) 2009–2010 . In: Derek, N, Krummel, PB and Cleland, SJ (eds.), 7–16. Melbourne, Australia: Australian Bureau of Meteorology and CSIRO Marine and Atmospheric Research.
Monks, PS, Granier, C, Fuzzi, S, Stohl, A, Williams, M, Akimoto, H, Amman, M, Baklanov, A, Baltensperger, U, Bey, I, Blake, N, Blake, RS, Carslaw, K, Cooper, OR, Dentener, F, Fragkou, E, Frost, G, Generoso, S, Ginoux, P, Grewe, V, Guenther, A, Hansson, HC, Henne, S, Hjorth, J, Hofzumahaus, A, Huntrieser, H, Jenkin, ME, Kaiser, J, Kanakidou, M, Klimont, Z, Kulmala, M, Lawrence, MG, Lee, JD, Liousse, C, McFiggans, G, Metzger, A, Mieville, A, Moussiopoulos, N, Orlando, JJ, O’Dowd, C, Palmer, PI, Parrish, DD, Petzold, A, Platt, U, Pöschl, U, Prévôt, ASH, Reeves, CE, Reiman, S, Rudich, Y, Sellegri, K, Steinbrecher, R, Simpson, D, ten Brink, H, Theloke, J, van der Werf, G, Vautard, R, Vestreng, V, Vlachokostas, CH and vonGlasow, R. 2009. Atmospheric Composition Change – Global and Regional Air Quality. Atmos. Environ ., 43: 5268–5350.
Monks, PS, Archibald, AT, Colette, A, Cooper, O, Coyle, M, Derwent, R, Fowler, D, Granier, C, Law, KS, Mills, GE, Stevenson, DS, Tarasova, O, Thouret, V, von Schneidemesser, E, Sommariva, R, Wild, O and Williams, ML. 2015. Tropospheric ozone and its precursors from the urban to the global scale from air quality to short-lived climate forcer. Atmos. Chem. Phys ., 15: 8889–8973. DOI: 10.5194/acp-15-8889-2015
Myhre, G, Aas, W, Cherian, R, Collins, W, Faluvegi, G, Flanner, M, Forster, P, Hodnebrog, Ø, Klimont, Z, Lund, MT and Mülmenstädt, J. 2017. Multi-model simulations of aerosol and ozone radiative forcing due to anthropogenic emission changes during the period 1990–2015. Atmospheric Chemistry and Physics 17(4): 2709–2720. DOI: 10.5194/acp-17-2709-2017
Nédélec, P, Blot, R, Boulanger, D, Athier, G, Cousin, J, Gautron, B, Petzold, A, Volz-Thomas, A and Thouret, V. 2015. Instrumentation on commercial aircraft for monitoring the atmospheric composition on a global scale: the IAGOS system, technical overview of ozone and carbon monoxide measurements. Tellus B 67. DOI: 10.3402/tellusb.v67.27791
Neis, P, Smit, HGJ, Krämer, M, Spelten, N and Petzold, A. 2015a. Evaluation of the MOZAIC Capacitive Hygrometer during the airborne field study CIRRUS-III. Atmos. Meas. Tech ., 8(3): 1233–1243. DOI: 10.5194/amt-8-1233-2015
Neis, P, Smi, H, Rohs, S, Bundke, U, Krämer, M, Spelten, N, Ebert, V, Buchholz, B, Thomas, K and Petzold, A. 2015b. Quality assessment of MOZAIC and IAGOS capacitive hygrometers: insights from airborne field studies. Tellus B 67. DOI: 10.3402/tellusb.v67.28320
Okamoto, S, Tanimoto, H, Hirota, N, Ikeda, K and Akimoto, H. 2018. Decadal shifts in wind patterns reduced continental outflow and suppressed ozone trend in the 2010s in the lower troposphere over Japan. Journal of Geophysical Research: Atmospheres 123(22): 12–980. DOI: 10.1029/2018JD029266
Oltmans, SJ and Komhyr, WD. 1976a. Air Resources Laboratories. Surface Ozone in Antarctica; Noaa Technical Memorandum, Erl Arl-56; Boulder, Colo: Air Resources Laboratory, Environmental Research Laboratories.
Oltmans, SJ and Komhyr, WD. 1976b. Surface ozone in Antarctica. J. Geophys. Res ., 81: 5359–5364. DOI: 10.1029/JC081i030p05359
Oltmans, SJ. 1981. Surface ozone measurements in clean air. J. Geophys. Res ., 86: 1174–1180. DOI: 10.1029/JC086iC02p01174
Oltmans, SJ and Komhyr, WD. 1986. Surface ozone distributions and variations from 1973–1984: Measurements at the NOAA Geophysical Monitoring for Climatic Change Baseline Observatories. Journal of Geophysical Research: Atmospheres 91(D4): 5229–5236. DOI: 10.1029/JD091iD04p05229
Oltmans, SJ and Levy II, H. 1994. Surface ozone measurements from a global network. Atmospheric Environment 28(1): 9–24. DOI: 10.1016/1352-2310(94)90019-1
Oltmans, S, Levy II, H, Harris, JM, Merrill, JT, Moody, JL, Lathrop, J, Cuevas, E, Trainer, M, O’Neill, MS, Prospero, JM, Vömel, H and Johnson, BJ. 1996. Summer and Spring Ozone Profiles Over the North Atlantic from Ozonesonde Measurements. J. Geophys. Res ., 101(D22): 29179–29200. DOI: 10.1029/96JD01713
Oltmans, SJ, Lefohn, AS, Harris, JM, Galbally, I, Scheel, HE, Bodeker, G, Brunke, E, Claude, H, Tarasick, D, Johnson, BJ, Simmonds, P, Shadwick, D, Anlauf, K, Hayden, K, Schmidlin, F, Fujimoto, T, Akagi, K, Meyer, C, Nichol, S, Davies, J, Redondas, A and Cuevas, E. 2006. Long-term Changes in Tropospheric Ozone. Atmos. Environ ., 40: 3156–3173. DOI: 10.1016/j.atmosenv.2006.01.029
Oltmans, SJ, Lefohn, AS, Scheel, HE, Harris, JM, Levy II, H, Galbally, IE, Brunke, E-G, Meyer, CP, Lathrop, JA, Johnson, BJ, Shadwick, DS, Cuevas, E, Schmidlin, FJ, Tarasick, DW, Claude, H, Kerr, JB, Uchino, O and Mohnen, V. 1998. Trends of ozone in the troposphere. Geophysical Research Letters , 25(2): 139–142. DOI: 10.1029/97GL03505
Oltmans, SJ, Lefohn, AS, Shadwick, D, Harris, JM, Scheel, H-E, Galbally, I, Tarasick, DW, Johnson, BJ, Brunke, EG, Claude, H, Zeng, G, Nichol, S, Schmidlin, FJ, Davies, J, Cuevas, E, Redondas, A, Naoe, H, Nakano, T and Kawasato, T. 2013. Recent Tropospheric Ozone Changes – A Pattern Dominated by Slow or No Growth. Atmospheric Environment 67: 331–351. DOI: 10.1016/j.atmosenv.2012.10.057
Parrish, DD, Law, KS, Staehelin, J, Derwent, R, Cooper, OR, Tanimoto, H, Volz-Thomas, A, Gilge, S, Scheel, H-E, Steinbacher, M and Chan, E. 2012. Long-term changes in lower tropospheric baseline ozone concentrations at northern mid-latitudes. Atmos. Chem. Phys 12: 11485–11504. DOI: 10.5194/acp-12-11485-2012
Parrish, DD, Lamarque, J-F, Naik, V, Horowitz, L, Shindell, DT, Staehelin, J, Derwent, R, Cooper, OR, Tanimoto, H, Volz-Thomas, A, Gilge, S, Scheel, H-E, Steinbacher, M and Fröhlich, M. 2014. Long-term changes in lower tropospheric baseline ozone concentrations: Comparing chemistry-climate models and observations at northern midlatitudes. J. Geophys. Res. Atmos ., 119. DOI: 10.1002/2013JD021435
Petetin, H, Thouret, V, Athier, G, Blot, R, Boulanger, D, Cousin, J-M, Gaudel, A, Nedelec, P and Cooper, O. 2016. Diurnal cycle of ozone throughout the troposphere over Frankfurt as measured by MOZAIC-IAGOS commercial aircraft. Elem Sci Anth ., 4: 129. DOI: 10.12952/journal.elementa.000129
Petetin, H, Jeoffrion, M, Sauvage, B, Athier, G, Blot, R, Boulanger, D, Clark, H, Cousin, J-M, Gheusi, F, Nedelec, P, Steinbacher, M and Thouret, V. 2018. Representativeness of the IAGOS airborne measurements in the lower troposphere. Elem Sci Anth 6: 23. DOI: 10.1525/elementa.280
Petzold, A, Thouret, V, Gerbig, C, Zahn, A, Brenninkmeijer, C, Gallagher, M, Hermann, M, Pontaud, M, Ziereis, H, Boulanger, D, Marshall, J, Nédélec, P, Smit, H, Friess, U, Flaud, J, Wahner, A, Cammas, J and Volz-Thomas, A. 2015. Global-scale atmosphere monitoring by in-service aircraft – current achievements and future prospects of the European Research Infrastructure IAGOS. Tellus B 67. DOI: 10.3402/tellusb.v67.28452
Price, S and Pales, JC. 1963. Mauna Loa Observatory: The first five years. Monthly Weather Review , Month: October–December , 1963. DOI: 10.1175/1520-0493(1963)091%3C0665:MLOTFF%3E2.3.CO;2
Prospero, JM, Schmitt, R, Cuevas, E, Savoie, D, Graustein, W, Turekian, K, Volz-Thomas, A, Diaz, A, Oltmans, S and Levy II, H. 1995. Temporal Variability of Summer-time Ozone and Aerosols in the Free Troposphere over the Eastern North Atlantic. Geophys. Res. Lett ., 22(21): 2925–2928. DOI: 10.1029/95GL02791
Rodríguez, S, Cuevas, E, Prospero, JM, Alastuey, A, Querol, X, López-Solano, J, García, MI and Alonso-Pérez, S. 2015. Modulation of Saharan dust export by the North African dipole. Atmos. Chem. Phys ., 15: 7471–7486, DOI: 10.5194/acp-15-7471-2015
Rodriguez, S, Torres, C, Guerra, JC and Cuevas, E. 2004. Transport Pathways to Ozone to Marine and Free-Troposphere Sites in Tenerife, Canary Islands. Atmos. Environ ., 38: 4733–4747. DOI: 10.1016/j.atmosenv.2004.05.021
Rodriguez-Franco, JJ and Cuevas, E. 2013. Characteristics of the subtropical tropopause region based on long-term highly-resolved sonde records over Tenerife. J. Geophys. Res. Atmos ., 118. DOI: 10.1002/jgrd.50839
Runge, C. 1901. Über empirische Funktionen und die Interpolation zwischen äquidistanten Ordinaten. Zeitschrift für Mathematik und Physik 46: 224–243. available at www.archive.org.
Saunois, M, Emmons, L, Lamarque, JF, Tilmes, S, Wespes, C, Thouret, V and Schultz, M. 2012. Impact of sampling frequency in the analysis of tropospheric ozone observations. Atmospheric chemistry and physics 12(15): 6757–6773. DOI: 10.5194/acp-12-6757-2012
Scheel, HE, Areskoug, H, Geiss, H, Gomiscek, B, Granby, K, Haszpra, L, Klasinc, L, Kley, D, Laurila, T, Lindskog, A and Roemer, M. 1997. On the spatial distribution and seasonal variation of lower-troposphere ozone over Europe. Journal of Atmospheric Chemistry 28(1–3). 11–28. DOI: 10.1023/A:1005882922435
Schultz, M. 1995. Die Bedeutung von Stickoxiden für die Ozonbilanz in Reinluftgebieten (Doctoral dissertation, Ph. D. thesis, Univ. of Wuppertal, Wuppertal, Germany).
Schultz, MG, Akimoto, H, Bottenheim, J, Buchmann, B, Galbally, IE, Gilge, S, Helmig, D, Koide, H, Lewis, AC, Novelli, PC, Plass-Dülmer, C, Ryerson, TB, Steinbacher, M, Steinbrecher, R, Tarasova, O, Tørseth, K, Thouret, V and Zellweger, C. 2015. The Global Atmosphere Watch reactive gases measurement network. Elem Sci Anth ., 3: 000067. DOI: 10.12952/journal.elementa.000067
Schultz, MG, Schröder, S, Lyapina, O, Cooper, O, Galbally, I, Petropavlovskikh, I, von Schneidemesser, E, Tanimoto, H, Elshorbany, Y, Naja, M, Seguel, R, Dauert, U, Eckhardt, P, Feigenspahn, S, Fiebig, M, Hjellbrekke, A-G, Hong, Y-D, Christian Kjeld, P, Koide, H, Lear, G, Tarasick, D, Ueno, M, Wallasch, M, Baumgardner, D, Chuang, M-T, Gillett, R, Lee, M, Molloy, S, Moolla, R, Wang, T, Sharps, K, Adame, JA, Ancellet, G, Apadula, F, Artaxo, P, Barlasina, M, Bogucka, M, Bonasoni, P, Chang, L, Colomb, A, Cuevas, E, Cupeiro, M, Degorska, A, Ding, A, Fröhlich, M, Frolova, M, Gadhavi, H, Gheusi, F, Gilge, S, Gonzalez, MY, Gros, V, Hamad, SH, Helmig, D, Henriques, D, Hermansen, O, Holla, R, Huber, J, Im, U, Jaffe, DA, Komala, N, Kubistin, D, Lam, K-S, Laurila, T, Lee, H, Levy, I, Mazzoleni, C, Mazzoleni, L, McClure-Begley, A, Mohamad, M, Murovic, M, Navarro-Comas, M, Nicodim, F, Parrish, D, Read, KA, Reid, N, Ries, L, Saxena, P, Schwab, JJ, Scorgie, Y, Senik, I, Simmonds, P, Sinha, V, Skorokhod, A, Spain, G, Spangl, W, Spoor, R, Springston, SR, Steer, K, Steinbacher, M, Suharguniyawan, E, Torre, P, Trickl, T, Weili, L, Weller, R, Xu, X, Xue, L and Zhiqiang, M. 2017. Tropospheric Ozone Assessment Report: Database and metrics data of global surface ozone observations. Elem Sci. Anth ., 5: 58. DOI: 10.1525/elementa.244
Seltzer, KM, Shindell, DT, Kasibhatla, P and Malley, CS. 2020. Magnitude, trends, and impacts of ambient long-term ozone exposure in the United States from 2000 to 2015. Atmos. Chem. Phys ., 20: 1757–1775. DOI: 10.5194/acp-20-1757-2020
Shen, L, Jacob, DJ, Liu, X, Huang, G, Li, K, Liao, H and Wang, T. 2019. An evaluation of the ability of the Ozone Monitoring Instrument (OMI) to observe boundary layer ozone pollution across China: application to 2005–2017 ozone trends. Atmos. Chem. Phys ., 19: 6551–6560. DOI: 10.5194/acp-19-6551-2019
Simon, H, Reff, A, Wells, B, Xing, J and Frank, N. 2015. Ozone Trends Across the United States over a Period of Decreasing NOx and VOC Emissions. Environ. Sci. Technol ., 49: 186–195. DOI: 10.1021/es504514z
Sofen, ED, Bowdalo, D and Evans, MJ. 2016. How to most effectively expand the global surface ozone observing network. Atmos. Chem. Phys ., 16: 1445–1457. DOI: 10.5194/acp-16-1445-2016
Solberg, S. 2003. Monitoring of boundary layer ozone in Norway from 1977 to 2002. Norwegian Institute for Air Research, NILU Report No. OR, 85/2003 . ISBN 82-425-1523-9, ISSN 0807-7207.
Stauffer, RM, Thompson, AM and Witte, JC. 2018. Characterizing global ozonesonde profile variability from surface to the UT/LS with a clustering technique and MERRA-2 reanalysis. Journal of Geophysical Research: Atmospheres 123(11): 6213–6229. DOI: 10.1029/2018JD028465
Steinbacher, M, Henne, S, Dommen, J, Wiesen, P and Prévôt, ASH. 2004. Nocturnal Trans-Alpine Transport of Ozone and its Effects on Air Quality on the Swiss Plateau. Atmospheric Environment 38: 4539–4550. DOI: 10.1016/j.atmosenv.2004.05.008
Strode, SA, Ziemke, JR, Oman, LD, Lamsal, LN, Olsen, MA and Liu, J. 2018. Global changes in the diurnal cycle of surface ozone. Atmos. Environ ., 199: 323–333. DOI: 10.1016/j.atmosenv.2018.11.028
Tarasick, DW, Davies, J, Smit, HGJ and Oltmans, SJ. 2016. A re-evaluated Canadian ozonesonde record: measurements of the vertical distribution of ozone over Canada from 1966 to 2013. Atmos. Meas. Tech ., 9: 195–214. DOI: 10.5194/amt-9-195-2016
Tarasick, DW, Galbally, IE, Cooper, OR, Schultz, MG, Ancellet, G, Leblanc, T, Wallington, TJ, Ziemke, J, Liu, X, Steinbacher, M, Staehelin, J, Vigouroux, C, Hannigan, JW, García, O, Foret, G, Zanis, P, Weatherhead, E, Petropavlovskikh, I, Worden, H, Osman, M, Liu, J, Chang, K-L, Gaudel, A, Lin, M, Granados-Muñoz, M, Thompson, AM, Oltmans, SJ, Cuesta, J, Dufour, G, Thouret, V, Hassler, B, Trickl, T and Neu, JL. 2019. Tropospheric Ozone Assessment Report: Tropospheric ozone from 1877 to 2016, observed levels, trends and uncertainties. Elem Sci Anth ., 7(1). DOI: 10.1525/elementa.376
Tarasova, OA, Senik, IA, Sosonkin, MG, Cui, J, Staehelin, J and Prévôt, ASH. 2009. Surface ozone at the Caucasian site Kislovodsk High Mountain Station and the Swiss Alpine site Jungfraujoch: data analysis and trends (1990–2006). Atmos. Chem. Phys ., 9: 4157–4175. DOI: 10.5194/acp-9-4157-2009
Thouret, V, Marenco, A, Logan, JA, Nédélec, P and Grouhel, C. 1998. Comparisons of ozone measurements from the MOZAIC airborne program and the ozone sounding network at eight locations. J. Geophys. Res ., 103(D19): 25695–25720, DOI: 10.1029/98JD02243
Tørseth, K, Aas, W, Breivik, K, Fjæraa, AM, Fiebig, M, Hjellbrekke, AG, Lund Myhre, C, Solberg, S and Yttri, KE. 2012. Introduction to the European Monitoring and Evaluation Programme (EMEP) and observed atmospheric composition change during 1972–2009. Atmos. Chem. Phys ., 12: 5447–5481. DOI: 10.5194/acp-12-5447-2012
Tressol, M, Ordonez, C, Zbinden, R, Brioude, J, Thouret, V, Mari, C, Nedelec, P, Cammas, J-P, Smit, H, Patz, H-W and Volz-Thomas, A. 2008. Air pollution during the 2003 European heat wave as seen by MOZAIC airliners. Atmos. Chem. Phys ., 8: 2133–2150. DOI: 10.5194/acp-8-2133-2008
van der A, RJ, Mijling, B, Ding, J, Koukouli, ME, Liu, F, Li, Q, Mao, H and Theys, N. 2017. Cleaning up the air: effectiveness of air quality policy for SO2 and NOx emissions in China. Atmos. Chem. Phys ., 17: 1775–1789. DOI: 10.5194/acp-17-1775-2017
Van Malderen, R, Allaart, MAF, De Backer, H, Smit, HGJ and De Muer, D. 2016. On instrumental errors and related correction strategies of ozonesondes: possible effect on calculated ozone trends for the nearby sites Uccle and De Bilt. Atmos. Meas. Tech ., 9: 3793–3816. DOI: 10.5194/amt-9-3793-2016
Vautard, R, Honore, C, Beekmann, M and Rouil, L. 2005. Simulation of ozone during the August 2003 heat wave and emission control scenarios. Atmospheric Environment 39(16): 2957–2967. DOI: 10.1016/j.atmosenv.2005.01.039
Von Storch, H and Zwiers, FW. 1999. Statistical Analysis in Climate Research . Cambridge University Press. DOI: 10.1007/978-3-662-03744-7_2
Wada, A, Matsueda, H, Sawa, Y, Tsuboi, K and Okubo, S. 2011. Seasonal variation of enhancement ratios of trace gases observed over 10 years in the western North Pacific. Atmospheric Environment 45(12): 2129–2137. DOI: 10.1016/j.atmosenv.2011.01.043
Wang, T, Dai, J, Lam, KS, Poon, CN and Brasseur, GP. 2019. Twenty-five years of lower tropospheric ozone observations in subtropical East Asia: The influence of emissions and weather patterns. Geophysical Research Letters 46. DOI: 10.1029/2019GL084459
Wang, T, Wei, XL, Ding, AJ, Poon, SC, Lam, KS, Li, YS, Chan, LY and Anson, M. 2009. Increasing surface ozone concentrations in the background atmosphere of Southern China, 1994–2007. Atmos. Chem. Phys ., 9: 6217–6227. DOI: 10.5194/acp-9-6217-2009
Wasserstein, RL and Lazar, NA. 2016. The ASA’s Statement on p-Values: Context, Process, and Purpose. The American Statistician 70: 129–133. DOI: 10.1080/00031305.2016.1154108
Wasserstein, RL, Schirm, AL and Lazar, NA. 2019. Moving to a World Beyond “p < 0.05”. The American Statistician 73(sup1): 1–19. DOI: 10.1080/00031305.2019.1583913
Weatherhead, EC, Bodeker, GE, Fassò, A, Chang, K, Lazo, JK, Clack, CT, Hurst, DF, Hassler, BJ, English, M and Yorgun, S. 2017. Spatial Coverage of Monitoring Networks: A Climate Observing System Simulation Experiment. J. Appl. Meteor. Climatol ., 56: 3211–3228. DOI: 10.1175/JAMC-D-17-0040.1
Weatherhead, EC, Reinsel, GC, Tiao, GC, Meng, XL, Choi, D, Cheang, WK, Keller, T, DeLuisi, J, Wuebbles, DJ, Kerr, JB and Miller, AJ. 1998. Factors affecting the detection of trends: Statistical considerations and applications to environmental data. Journal of Geophysical Research: Atmospheres , 103(D14): 17149–17161. DOI: 10.1029/98JD00995
Weiss-Penzias, P, Jaffe, DA, Swartzendruber, P, Dennison, JB, Chand, D, Hafner, W and Prestbo, E. 2006. Observations of Asian air pollution in the free troposphere at Mount Bachelor Observatory during the spring of 2004. J. Geophys. Res ., 111: D10304. DOI: 10.1029/2005JD006522
WCC-Empa. 2019. https://www.empa.ch/web/s503/wcc-empa.
Worden, H, Bowman, K, Kulawik, S and Aghedo, A. 2011. Sensitivity of outgoing longwave radiative flux to the global vertical distribution of ozone characterized by instantaneous radiative kernels from Aura-TES. J. Geophys. Res ., 116: D14115. DOI: 10.1029/2010JD015101
Worden, HM, Bowman, KW, Worden, JR, Eldering, A and Beer, R. 2008. Satellite measurements of the clear-sky greenhouse effect from tropospheric ozone. Nat. Geosci ., 1: 305–308. DOI: 10.1038/ngeo182
Xu, W, Lin, W, Xu, X, Tang, J, Huang, J, Wu, H and Zhang, X. 2016. Long-term trends of surface ozone and its influencing factors at the Mt Waliguan GAW station, China–Part 1: Overall trends and characteristics. Atmospheric Chemistry and Physics 16(10): 6191–6205. DOI: 10.5194/acp-16-6191-2016
Young, PJ, Archibald, AT, Bowman, KW, Lamarque, J-F, Naik, V, Stevenson, DS, Tilmes, S, Voulgarakis, A, Wild, O, Bergmann, D, Cameron-Smith, P, Cionni, I, Collins, WJ, Dalsøren, SB, Doherty, RM, Eyring, V, Faluvegi, G, Horowitz, LW, Josse, B, Lee, YH, MacKenzie, IA, Nagashima, T, Plummer, DA, Righi, M, Rumbold, ST, Skeie, RB, Shindell, DT, Strode, SA, Sudo, K, Szopa, S and Zeng, G. 2013a. Pre-industrial to end 21st century projections of tropospheric ozone from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP). Atmos. Chem. Phys ., 13: 2063–2090. DOI: 10.5194/acp-13-2063-2013
Young, PJ, Archibald, AT, Bowman, KW, Lamarque, J-F, Naik, V, Stevenson, DS, Tilmes, S, Voulgarakis, A, Wild, O, Bergmann, D, Cameron-Smith, P, Cionni, I, Collins, WJ, Dalsøren, SB, Doherty, RM, Eyring, V, Faluvegi, G, Horowitz, LW, Josse, B, Lee, YH, MacKenzie, IA, Nagashima, T, Plummer, DA, Righi, M, Rumbold, ST, Skeie, RB, Shindell, DT, Strode, SA, Sudo, K, Szopa, S and Zeng, G. 2013b. Corrigendum to “Pre-industrial to end 21st century projections of tropospheric ozone from the Atmospheric Chemistry and Climate Model Intercomparison Project (ACCMIP)” published in Atmos. Chem. Phys., 13, 2063–2090. 2013. Atmos. Chem. Phys ., 13: 5401–5402. DOI: 10.5194/acp-13-5401-2013
Young, PJ, Naik, V, Fiore, AM, Gaudel, A, Guo, J, Lin, MY, Neu, JL, Parrish, DD, Rieder, HE, Schnell, JL, Tilmes, S, Wild, O, Zhang, L, Ziemke, JR, Brandt, J, Delcloo, A, Doherty, RM, Geels, C, Hegglin, MI, Hu, L, Im, U, Kumar, R, Luhar, A, Murray, L, Plummer, D, Rodriguez, J, Saiz-Lopez, A, Schultz, MG, Woodhouse, MT and Zeng, G, 2018. Tropospheric Ozone Assessment Report: Assessment of global-scale model performance for global and regional ozone distributions, variability, and trends. Elem Sci Anth 6(1): 10. DOI: 10.1525/elementa.265
Yuan, Y, Ries, L, Petermeier, H, Steinbacher, M, Gómez-Peláez, AJ, Leuenberger, MC, Schumacher, M, Trickl, T, Couret, C, Meinhardt, F and Menzel, A. 2018. Adaptive selection of diurnal minimum variation: a statistical strategy to obtain representative atmospheric CO2 data and its application to European elevated mountain stations. Atmos. Meas. Tech ., 11: 1501–1514. DOI: 10.5194/amt-11-1501-2018
Yuan, Y, Ries, L, Petermeier, H, Trickl, T, Leuchner, M, Couret, C, Sohmer, R, Meinhardt, F and Menzel, A. 2019a. On the diurnal, weekly, and seasonal cycles and annual trends in atmospheric CO2 at Mount Zugspitze, Germany, during 1981–2016. Atmos. Chem. Phys ., 19: 999–1012. DOI: 10.5194/acp-19-999-2019
Yuan, Y, Sussmann, R, Rettinger, M, Ries, L, Petermeier, H and Menzel, A. 2019b. Comparison of Continuous In-Situ CO2 Measurements with Co-Located Column-Averaged XCO2 TCCON/Satellite Observations and CarbonTracker Model Over the Zugspitze Region. Remote Sensing 11(24): 2981. DOI: 10.3390/rs11242981
Zanis, P, Schuepbach, E, Scheel, H, Baudenbacher, M and Buchmann, B. 1999. Inhomogeneity and trends in the surface ozone record (1988–1996) at Jungfraujoch in the Swiss Alps. Atmos. Environ ., 33: 3777–3786. DOI: 10.1016/S1352-2310(99)00088-6
Zellweger, C, Forrer, J, Hofer, P, Nyeki, S, Schwarzenbach, B, Weingartner, E, Ammann, M and Baltensperger, U. 2003. Partitioning of reactive nitrogen (NOy) and dependence on meteorological conditions in the lower free troposphere. Atmospheric Chemistry and Physics 3(3): 779–796. DOI: 10.5194/acp-3-779-2003
Zellweger, C, Hüglin, C, Klausen, J, Steinbacher, M, Vollmer, M and Buchmann, B. 2009. Inter-comparison of four different carbon monoxide measurement techniques and evaluation of the long-term carbon monoxide time series of Jungfraujoch. Atmospheric Chemistry and Physics 9(11): 3491–3503. DOI: 10.5194/acp-9-3491-2009
Zellweger, C, Steinbacher, M and Buchmann, B. 2011. System and performance audit of surface ozone, methane, carbon dioxide, nitrous oxide and carbon monoxide at the Global GAW Station Zugspitze-Schneefernerhaus, Germany, June 2011, WCC-Empa Report 11/2. https://www.empa.ch/web/s503/wcc-empa.
Zhang, Y, Cooper, OR, Gaudel, A, Thompson, AM, Nédélec, P, Ogino, S-Y and West, JJ. 2016. Tropospheric ozone change from 1980 to 2010 dominated by equatorward redistribution of emissions. Nature Geoscience 9(12): 875. DOI: 10.1038/ngeo2827
Ziemke, JR, Oman, LD, Strode, SA, Douglass, AR, Olsen, MA, McPeters, RD, Bhartia, PK, Froidevaux, L, Labow, GJ, Witte, JC, Thompson, AM, Haffner, DP, Kramarova, NA, Frith, SM, Huang, L-K, Jaross, GR, Seftor, CJ, Deland, MT and Taylor, SL. 2019. Trends in global tropospheric ozone inferred from a composite record of TOMS/OMI/MLS/OMPS satellite measurements and the MERRA-2 GMI simulation. Atmos. Chem. Phys ., 19: 3257–3269. DOI: 10.5194/acp-19-3257-2019
Zwiers, FW and Von Storch, H. 2004. On the role of statistics in climate research. International Journal of Climatology: A Journal of the Royal Meteorological Society 24(6): 665–680. DOI: 10.1002/joc.1027