<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing with OASIS Tables v3.0 20080202//EN" "journalpub-oasis3.dtd">
<article xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:oasis="http://docs.oasis-open.org/ns/oasis-exchange/table" dtd-version="3.0">
  <front>
    <journal-meta>
<journal-id journal-id-type="publisher">ACP</journal-id>
<journal-title-group>
<journal-title>Atmospheric Chemistry and Physics</journal-title>
<abbrev-journal-title abbrev-type="publisher">ACP</abbrev-journal-title>
<abbrev-journal-title abbrev-type="nlm-ta">Atmos. Chem. Phys.</abbrev-journal-title>
</journal-title-group>
<issn pub-type="epub">1680-7324</issn>
<publisher><publisher-name>Copernicus Publications</publisher-name>
<publisher-loc>Göttingen, Germany</publisher-loc>
</publisher>
</journal-meta>

    <article-meta>
      <article-id pub-id-type="doi">10.5194/acp-17-6477-2017</article-id><title-group><article-title><?xmltex \hack{\vspace{-3.5mm}}?>Surface ozone in the Southern Hemisphere: 20 years of data from a site with
a unique setting in El Tololo, Chile</article-title>
      </title-group><?xmltex \runningtitle{20~years of ozone data from El Tololo, Chile}?><?xmltex \runningauthor{J.~G.~Anet et al.}?>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes" rid="aff1 aff2">
          <name><surname>Anet</surname><given-names>Julien G.</given-names></name>
          <email>julien.anet@bluewin.ch</email>
        <ext-link>https://orcid.org/0000-0002-2949-1363</ext-link></contrib>
        <contrib contrib-type="author" corresp="yes" rid="aff1">
          <name><surname>Steinbacher</surname><given-names>Martin</given-names></name>
          <email>martin.steinbacher@empa.ch</email>
        <ext-link>https://orcid.org/0000-0002-7195-8115</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3 aff4">
          <name><surname>Gallardo</surname><given-names>Laura</given-names></name>
          
        <ext-link>https://orcid.org/0000-0001-7605-3721</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff5 aff6">
          <name><surname>Velásquez Álvarez</surname><given-names>Patricio A.</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-7835-9094</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Emmenegger</surname><given-names>Lukas</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-9812-3986</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Buchmann</surname><given-names>Brigitte</given-names></name>
          
        </contrib>
        <aff id="aff1"><label>1</label><institution>Laboratory for Air Pollution/Environmental Technology, Swiss Federal Laboratories for Materials Science and Technology Empa, Duebendorf, Switzerland</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>WSL Institute for Snow and Avalanche Research SLF, Davos, Switzerland</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>Departamento de Geofísica de la Universidad de Chile, Blanco Encalada 2002, piso 4, Santiago, Chile</institution>
        </aff>
        <aff id="aff4"><label>4</label><institution>Center for Climate and Resilience Research (CR2), Blanco Encalada 2002, Santiago, Chile</institution>
        </aff>
        <aff id="aff5"><label>5</label><institution>Dirección Meteorológica de Chile, Av. Portales 3450, Estación Central, Santiago, Chile</institution>
        </aff>
        <aff id="aff6"><label>6</label><institution>Climate and Environmental Physics, Physics Institute, University of Bern, Bern, Switzerland</institution>
        </aff>
      </contrib-group>
      <author-notes><corresp id="corr1">Julien G. Anet (julien.anet@bluewin.ch) and Martin Steinbacher (martin.steinbacher@empa.ch)</corresp></author-notes><pub-date><day>31</day><month>May</month><year>2017</year></pub-date>
      
      <volume>17</volume>
      <issue>10</issue>
      <fpage>6477</fpage><lpage>6492</lpage>
      <history>
        <date date-type="received"><day>12</day><month>July</month><year>2016</year></date>
           <date date-type="rev-request"><day>7</day><month>October</month><year>2016</year></date>
           <date date-type="rev-recd"><day>24</day><month>March</month><year>2017</year></date>
           <date date-type="accepted"><day>25</day><month>April</month><year>2017</year></date>
      </history>
      <permissions>
<license license-type="open-access">
<license-p>This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/3.0/">http://creativecommons.org/licenses/by/3.0/</ext-link></license-p>
</license>
</permissions><self-uri xlink:href="https://acp.copernicus.org/articles/.html">This article is available from https://acp.copernicus.org/articles/.html</self-uri>
<self-uri xlink:href="https://acp.copernicus.org/articles/.pdf">The full text article is available as a PDF file from https://acp.copernicus.org/articles/.pdf</self-uri>


      <abstract>
    <p>The knowledge of surface ozone mole fractions and their global distribution
is of utmost importance due to the impact of ozone on human health and
ecosystems and the central role of ozone in controlling the oxidation
capacity of the troposphere. The availability of long-term ozone records is
far better in the Northern than in the Southern Hemisphere, and recent
analyses of the seven accessible records in the Southern Hemisphere have
shown inconclusive trends. Since late 1995, surface ozone is measured in situ
at “El Tololo”, a high-altitude (2200 <inline-formula><mml:math id="M1" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> a.s.l.) and pristine
station in Chile (30<inline-formula><mml:math id="M2" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> S, 71<inline-formula><mml:math id="M3" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> W). The dataset has been
recently fully quality controlled and reprocessed. This study presents the
observed ozone trends and annual cycles and identifies key processes driving
these patterns. From 1995 to 2010, an overall positive trend of
<inline-formula><mml:math id="M4" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula> 0.7 <inline-formula><mml:math id="M5" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula> is found. Strongest trends per season
are observed in March and April. Highest mole fractions are observed in late
spring (October) and show a strong correlation with ozone transported from
the stratosphere down into the troposphere, as simulated with a model. Over
the 20 years of observations, the springtime ozone maximum has shifted to
earlier times in the year, which, again, is strongly correlated with a
temporal shift in the occurrence of the maximum of simulated stratospheric
ozone transport at the site. We conclude that background ozone at El Tololo
is mainly driven by stratospheric intrusions rather than photochemical
production from anthropogenic and biogenic precursors. The major footprint of
the sampled air masses is located over the Pacific Ocean. Therefore, due to
the negligible influence of local processes, the ozone record also allows
studying the influence of El Niño and La Niña episodes on background
ozone levels in South America. In agreement with previous studies, we find
that, during La Niña conditions, ozone mole fractions reach higher levels
than during El Niño conditions.</p>
  </abstract>
    </article-meta>
  </front>
<body>
      

<sec id="Ch1.S1" sec-type="intro">
  <title>Introduction</title>
      <p>Tropospheric ozone (<inline-formula><mml:math id="M6" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>) is a key atmospheric compound
that plays an important role in many respects: it acts as a greenhouse gas,
which is contributing to radiative forcing of up to 21 % relative to the
radiative forcing induced by <inline-formula><mml:math id="M7" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> (Myhre et al., 2013). Ozone has
adverse effects on crop yields and on human health, being an irritating agent
and triggering asthma and cardiovascular diseases (Reich and Amundson, 1985;
Brook, 2002; Fiscus et al., 2005). Ozone is also a major source of
hydroxyradicals and, thereby, influences the oxidative capacity of the
atmosphere (Crutzen, 1971; Staehelin et al., 2001).</p>
      <p>Various processes determine the amount of ozone in the troposphere: ozone is
naturally produced by oxidation of methane, by reaction of oxygen with
lightning-induced NO production, as well as by photochemical formation in the
presence of volatile organic compounds (VOCs), nitrogen oxides
(<inline-formula><mml:math id="M8" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M9" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>), and sunlight (Crutzen, 1971, 1973; Crutzen and Zimmermann,
1991; Winer et al., 1992; Derwent et al., 1998). Thus, changes in ozone
precursor emissions – which are partly due to anthropogenic activities –
considerably influence the tropospheric ozone burden. However, a
straightforward attribution of emission changes to ozone trends is
challenging due to the highly nonlinear photochemistry, different (VOC- and
<inline-formula><mml:math id="M10" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M11" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>-limited) ozone production regimes, and also photochemical loss
processes (Crutzen, 1971; Sillman and He, 2002). A significant part of
tropospheric ozone originates from stratosphere–troposphere transport (STT),
also known as stratosphere–troposphere exchange (STE), happening, e.g., in
tropopause folds (Holton et al., 1995; Škerlak, 2014; Škerlak et
al., 2014; Lefohn and Cooper, 2015). The STE is not evenly distributed over
the globe and hotspots of transport of stratospheric ozone into the planetary
boundary layer exist in the region of the Rocky Mountains, Tibetan Plateau,
Andes (around 30<inline-formula><mml:math id="M12" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> S), storm tracks, and Indian Ocean (Škerlak et
al., 2014). Recent modeling studies postulate that the contribution from STE
to the tropospheric ozone burden may be as high as 23 % of the net
photochemical production (Stevenson et al., 2006; Sudo and Akimoto, 2007).
This contribution may change in the future due to climate change and could
lead to more than 20 % STE increase (Collins et al., 2003; Hegglin and
Shepherd, 2009; Neu et al., 2014).</p>
      <p>Ozone sinks include catalytic destruction involving <inline-formula><mml:math id="M13" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">HO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> and
photolytic destruction; <inline-formula><mml:math id="M14" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> can also be removed from the atmosphere by
dry deposition, wet scavenging, and uptake by vegetation (Galbally, 1968;
Stevenson et al., 2006).</p>
      <p>The first ozone observations in the atmosphere were performed in the 19th
century in Montsouris, Paris (Volz and Kley, 1988). However, regular and
geographically distributed measurements have become more established only in
the second half of the 20th century. Nowadays, surface ozone observations are
widespread and data are available from various data repositories such as the
World Data Centre for Greenhouse Gases (WDCGG) of the Global Atmospheric
Watch (GAW) programme of WMO or from regional environmental agencies like the
European Environment Agency (AirBase), the US Environmental Protection Agency
(CASTNET, AQS), and the Acid Deposition Monitoring Network in East Asia
(EANET). Currently, observations in the Southern Hemisphere (SH) in general,
and in South America in particular, are very sparse (Sofen et al., 2016a, b).</p>
      <p>Following Parrish et al. (2012), Oltmans et al. (2013), and Cooper et
al. (2014), emissions of anthropogenic volatile organic compound and
hydrocarbon emissions have led to a strong rise of ozone production in the
last century. In fact, ozone has been generally increasing by up to 3 and
7 <inline-formula><mml:math id="M15" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula> in the SH and Northern Hemisphere (NH),
respectively, averaged over different time spans (all between 1971 and 2011
and at least averaged over 10 years; see, e.g., Table 1 of Cooper et
al., 2014). Thorough research has been undertaken to explain the difference
in the trends between the two hemispheres. The more pronounced trend in the
NH can possibly be explained by (i) higher precursor emissions than in the SH
and (ii) relatively short lifetime of ozone and subsequent lack of transport
into the SH. Moreover, trends in the NH are very different from location to
location. Recent work raised the attention to the flattening of the positive
trend in NH tropospheric ozone at certain sites, especially at those located
in Europe or eastern North America (Cooper et al., 2014). At most stations,
this finding can be explained by decreasing nitrogen oxides (<inline-formula><mml:math id="M16" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M17" display="inline"><mml:mrow><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub><mml:mo>=</mml:mo></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M18" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M19" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> <inline-formula><mml:math id="M20" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">NO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>) emissions in the developed western
countries. Such a leveling off is currently not observed in the western
United States as <inline-formula><mml:math id="M21" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M22" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula> sources in upstream regions such as eastern
Asia are still significantly increasing (Cooper et al., 2012). In contrast,
the few SH ozone monitoring stations only partly recorded a flattening of the
trend (Cooper et al., 2014). These ozone time series show either increasing
positive trends (Oltmans et al., 2013; Thompson et al., 2014) or no
significant change at all (Oltmans et al., 2013; Cooper et al., 2014). A
worldwide map of ozone trends interpolated from the existing surface ozone
measurement stations is not yet available. Wespes et al. (2016) recently
tried to map ozone mixing ratio trends in the lower troposphere by using
remote sensing satellite data from 2008 to 2013. They showed that ozone
mixing ratios in the lower troposphere were generally decreasing all over the
SH and in most parts of the NH during this period. However, this trend cannot
be generalized as polluted areas of the world still show significant positive
ozone trends.</p>
      <p>Tropospheric ozone records often show a pronounced seasonal cycle. While in
polluted areas a strong photochemically driven summer peak is observed, a
spring peak with stratospheric influence dominates in most continental
pristine regions (Wang et al., 1998a, b; Monks, 2000). Stations in the marine
boundary layer in the SH such as Cape Grim, Australia, rarely reveal a
distinct spring peak but rather show a summer peak due to <inline-formula><mml:math id="M23" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">HO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>
photochemistry (Ayers et al., 1992; Monks, 2000). Measurements in the SH free
troposphere (e.g., La Quiaca, Argentina; 3459 <inline-formula><mml:math id="M24" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> a.s.l.) show a
spring maximum (Barlasina et al., 2013) similar to the NH ozone time series
from unpolluted stations. These findings were more broadly confirmed by
Cooper et al. (2014), who, using satellite-measured total column ozone
datasets, classified the onsets of the total column ozone (<inline-formula><mml:math id="M25" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">TCO</mml:mi></mml:mrow></mml:math></inline-formula>) maxima
globally. In general, spring <inline-formula><mml:math id="M26" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">TCO</mml:mi></mml:mrow></mml:math></inline-formula> maxima are found rather on the SH,
while summer TCO maxima are prominent in the NH. This latter work is in
contrast to the results of Monks (2000), who concluded that the spring
phenomenon is primarily a NH feature. Wang et al. (1998a) and, more recently,
Lin et al. (2015) state that at least some NH spring peaks originate from a
combination of ozone-rich stratospheric influx (February–April) and
formation by local ozone chemistry (April–June). A recent analysis of the
ozone seasonal cycle at northern midlatitudes revealed a shift of these ozone
spring peak concentrations backwards by 3 to 6 days per decade (Parrish et
al., 2013). They conclude that this feature may be explained by changes in
atmospheric dynamics, possibly combined with variations in the geographical
distribution of the precursor emissions.</p>
      <p>At low latitudes, tropospheric ozone levels at remote sites are known to be
sensitive to teleconnections like the El Niño/Southern Oscillation
(ENSO). For example, Lin et al. (2014) analyzed the seasonal cycle of a
long-term ozone dataset from Mauna Loa (MLO, Hawaii), a tropical station in
the Pacific. There, long-term springtime ozone observations only marginally
increased in the 2000s whereas fall ozone was observed to significantly
augment in the 1990s. Lin et al. (2015) found the cause to be the ENSO,
which, by altering SST, convection, and large-scale atmospheric patterns,
reduced (augmented) advection of air masses from Asia in spring (fall) during
La Niña (El Niño) events. In the extratropics, the opposite is found:
springtime ozone levels have increased over time. Lin et al. (2015) explain
this discrepancy with ENSO-driven decadal shifts in the atmospheric dynamics,
leading to cooling pattern in the eastern Pacific equatorial region. The
ENSO-sensitive pattern limits itself not only to tropospheric ozone but also
to <inline-formula><mml:math id="M27" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">TCO</mml:mi></mml:mrow></mml:math></inline-formula>, as has been shown in Ziemke et al. (2010), who retrieved an
independent ENSO index based on TCO anomalies in the pacific region (Ozone
ENSO index, OEI).</p>
      <p>The GAW ozone network has a satisfactory station coverage over the NH. This
is not the case for the SH, where the network is very sparse and additional
surface ozone time series are needed to understand the global picture of
ozone dynamics. This paper describes a recently quality controlled 20-year
surface ozone dataset from “El Tololo”, a midlatitudes, subtropical
mountain site in Chile, South America, where ozone and a standard set of
meteorological variables have been measured since 1995. Recently, the station
has been equipped with a new ozone monitor and a <inline-formula><mml:math id="M28" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">CO</mml:mi></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M29" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>, and
<inline-formula><mml:math id="M30" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CH</mml:mi><mml:mn mathvariant="normal">4</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> analyzer by Empa (Swiss Federal Laboratories for Materials
Science and Technology).</p>
      <p>El Tololo is currently the only GAW station in the SH above the marine
boundary layer regularly submitting tropospheric ozone data to WDCGG.
Therefore, the station provides highly valuable information on the ozone
distribution in the unpolluted atmosphere. Gallardo et al. (2000) and
Rondanelli et al. (2002) published analyses of the early phase of the ozone
record, pointing at particular characteristics of the ozone time series in
connection with large-scale Hadley circulation, cutoff lows, and deep troughs
or related to transport from the boundary layer.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F1"><caption><p>Position of El Tololo, La Serena, Valparaíso, and Santiago de
Chile including topographic information. Terrain data source: NOAA ETOPO1,
plotted using marmap (Pante and Simon-Bouhet, 2013).</p></caption>
        <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f01.jpg"/>

      </fig>

      <p>The main objectives of this study are to characterize the complete time
series of this station, which is likely representative of a large domain of
the background SH, and to provide insight into the key processes driving the
observed variability and trends. Section 2 gives an overview of the
measurement station and the instrumentation. In Sect. 3, the data series are
presented and interpreted. Finally, we present our conclusions in the last
section.</p>
</sec>
<sec id="Ch1.S2">
  <title>Station characterization</title>
<sec id="Ch1.S2.SS1">
  <title>Location</title>
      <p>The atmospheric monitoring station “El Tololo” (TLL) is located in the
Coquimbo region at 2200 <inline-formula><mml:math id="M31" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> a.s.l., 30<inline-formula><mml:math id="M32" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>10<inline-formula><mml:math id="M33" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> S,
70<inline-formula><mml:math id="M34" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>47<inline-formula><mml:math id="M35" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> W, 400 km north of Santiago de Chile, around 90 <inline-formula><mml:math id="M36" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula>
below the top of the mountain Cerro Tololo. At Cerro Tololo, astronomical
telescopes and instruments are operated as the Cerro Tololo Inter-American
Observatory (CTIO), which belongs to the US National Optical Astronomy
Observatory (NOAO). The Chilean Meteorological Service (Dirección
Meteorológica de Chile, DMC) runs the El Tololo station on the CTIO area.
The distance from El Tololo to the next bigger cities is 50 <inline-formula><mml:math id="M37" display="inline"><mml:mi mathvariant="normal">km</mml:mi></mml:math></inline-formula> to the
NW (La Serena, Coquimbo) with smaller towns nearby (Vicuña, 20 <inline-formula><mml:math id="M38" display="inline"><mml:mi mathvariant="normal">km</mml:mi></mml:math></inline-formula>
NE; Paiguano, 30 <inline-formula><mml:math id="M39" display="inline"><mml:mi mathvariant="normal">km</mml:mi></mml:math></inline-formula> NE; Andacollo, 30 <inline-formula><mml:math id="M40" display="inline"><mml:mi mathvariant="normal">km</mml:mi></mml:math></inline-formula> SW; Ovalle,
60 <inline-formula><mml:math id="M41" display="inline"><mml:mi mathvariant="normal">km</mml:mi></mml:math></inline-formula> SW; see Fig. 1). Fifteen kilometers north of El Tololo, the
Elqui Valley, which is dominated by agricultural activity, is located in a
W–E elongation. The population density of this region is low: 17 inhabitants
per km<inline-formula><mml:math id="M42" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:math></inline-formula>.</p><?xmltex \hack{\newpage}?>
</sec>
<sec id="Ch1.S2.SS2">
  <title>Climatology</title>
      <p>Climate at TLL is classified as cool and arid. Between 1995 and 2015, the
average temperature was 13.4 <inline-formula><mml:math id="M43" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>C (see Fig. S3 in the Supplement) and,
in most years, less than 70 <inline-formula><mml:math id="M44" display="inline"><mml:mi mathvariant="normal">mm</mml:mi></mml:math></inline-formula> of rainfall was registered, which
classifies climate as a “desert climate” (BWk) following Köppen climate
classification of Geiger (1961) and Kottek et al. (2006). The wind measured
at TLL mostly blows from the SSW sector during the summer months (December,
January, and February, DJF) and from the NNE sector during the remaining time
of the year (see Fig. S4). However, the wind direction data do not
necessarily represent the free atmosphere, as the local topography at the
station partially obstructs advection from the NW to N sectors. Moreover,
turbulent eddies downwind of the mountain top influence the measured wind
direction. Kalthoff et al. (2002) described the mesoscale wind regimes
affecting the area.</p>
      <p>In order to identify the main origin of the air masses arriving at TLL,
backward trajectory simulations from the FLEXTRA model (e.g., Stohl et
al., 1995), calculated at Empa, were used. The model uses wind fields from
the European Centre for Medium-Range Weather Forecasts (ECMWF), and
subsequent analysis locates the source of the trajectories in the
northwestern to southern sector with some rare events from the north and
southeast (see Fig. 2). The influence of air parcels from the northeastern
parts of South America is minor since the Andes are efficiently blocking any
advection of air masses from this direction. Therefore, local pollution
events from the greater Santiago de Chile region are more relevant than
large-scale pollution events originating, e.g., from biomass burning in the
Amazon region. 71 % of the 10-day-trajectories start at an altitude
between 0 and 5000 <inline-formula><mml:math id="M45" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula>, and 10 % of the 10-day-trajectories
originate from altitudes higher than 8000 <inline-formula><mml:math id="M46" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> (see Fig. S5). The
origins of the trajectories follow clearly distinguishable seasonal patterns:
during the summer months (DJF), most trajectories originate from south of the
station and from the lower troposphere. During the winter months (JJA), more
trajectories start north of the station, as the southeastern pacific high
shifts to more northern latitudes at that time of the year (e.g., Rahn and
Garreaud, 2014). This also explains why trajectories from the upper
troposphere are more frequent in JJA compared to DJF (<inline-formula><mml:math id="M47" display="inline"><mml:mrow><mml:mo>+</mml:mo><mml:mn mathvariant="normal">50</mml:mn></mml:mrow></mml:math></inline-formula> %), following
increased subsidence. The mean air trajectory length is highest during spring
time (SON) and lowest during fall (MAM, see Fig. S6).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F2"><caption><p>FLEXTRA trajectory footprint from April 2013 to December 2015,
originating at El Tololo (TLL), 370 <inline-formula><mml:math id="M48" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> above model topography. Color
indicates the total residence time of air parcels, summed up over the time
period. TLL is marked with a black dot.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f02.pdf"/>

        </fig>

      <p>Being located in the subtropics, TLL is rarely affected by frontal or
cyclonic systems. Nevertheless, during spring and summer time (SON, DJF),
cutoff lows and troughs from higher latitude may reach subtropical regions,
thus influencing the large-scale advection patterns at TLL (Rondanelli et
al., 2002) on short timescales. This leads both to advection of polar air
masses as well as upward transport of marine boundary layer air potentially
polluted by human activities in the nearby cities, possibly influencing the
chemical composition of the air at TLL.</p>
      <p>Apart from meteorological frontal systems, climatological patterns like the
ENSO do influence the large-scale origin of air masses arriving at TLL. In
Fig. 3, the wind climatology and the change in the wind field during an
exemplary strong El Niño (1997–1998) and La Niña (1988–1989) event
are shown for austral spring and austral fall (ERA-Interim reanalysis (ERAI),
700 hPa wind, climatology from 1979 to 2015; see Sect. 4.3 for details).</p>
      <p>The subtropical Pacific high determines subsidence in the Tololo area
year-round, interrupted occasionally by passing fronts or cutoff lows
(Fuenzalida et al., 2005). It also drives a low-level jet (LLJ) along the
west coast of South America, which peaks in intensity in spring (Garreaud and
Muñoz, 2005; Muñoz and Garreaud, 2005). During El Niño (La
Niña) years, the Pacific high becomes weaker (stronger), which leads to
negative (positive) anomalies in subsidence and coastal southerly winds.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F3" specific-use="star"><caption><p>ERAI wind climatology at 700 <inline-formula><mml:math id="M49" display="inline"><mml:mi mathvariant="normal">hPa</mml:mi></mml:math></inline-formula> (<bold>a</bold>  MAM and
<bold>b</bold> SON) and wind change in vector and strength during an exemplary El
Niño event (1997–1998) (<bold>c</bold> MAM and <bold>d</bold> SON) and a La
Niña event (1988–1989) (<bold>e</bold> MAM and
<bold>f</bold> SON).</p></caption>
          <?xmltex \igopts{width=483.69685pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f03.png"/>

        </fig>

      <p>As mentioned earlier, ozone transport due to STE is an important factor of
the tropospheric <inline-formula><mml:math id="M50" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> burden particularly in the remote SH. The ERAI
climatology shows a “hotspot” of downward transport of stratospheric,
ozone-rich air masses above TLL (see Fig. 2 in Škerlak et al., 2014),
especially during austral spring and summer. This can most probably only be
explained by gravity wave triggering when air parcels originating from the
southern pacific region suddenly encounter a strong change in orographic
height (Andean barrier, up to 6000 <inline-formula><mml:math id="M51" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> a.s.l.). Moreover, the
weakening of the subtropical jet stream in DJF favors additional wave
breaking, triggering downward transport of ozone through tropopause folds.
This potentially leads to a higher burden of tropospheric ozone in DJF. We
will discuss this subject more thoroughly later in this work.</p><?xmltex \hack{\newpage}?>
</sec>
</sec>
<sec id="Ch1.S3">
  <title>Data and methods</title>
<sec id="Ch1.S3.SS1">
  <title>Ozone data at El Tololo</title>
      <p>In 1995, TLL has been equipped with an ozone photometer and a set of
meteorological sensors. Ozone at TLL is measured by UV absorption with a
Thermo Environmental Instruments Inc. TECO 49-003 analyzer. The station is
equipped with an external ozonator which allows producing defined levels of
ozone to conduct performance checks. Measurements are done continuously and
data are recorded on a Campbell Scientific 21X data logger as 15 min
averages. Zero and span checks on multiple levels are done twice weekly and
once monthly, respectively, to keep track of the background signal and the
instrument response. Regularly, the operator visually inspects the recorded
data for obvious anomalies.</p>
      <p>The TECO 49-003 analyzer measures the UV light absorption in the Hartley band
(220–310 <inline-formula><mml:math id="M52" display="inline"><mml:mi mathvariant="normal">nm</mml:mi></mml:math></inline-formula>) where ozone is a strong absorber. The optical bench is
a dual-cell device which is connected to a mercury lamp (245 <inline-formula><mml:math id="M53" display="inline"><mml:mi mathvariant="normal">nm</mml:mi></mml:math></inline-formula>) as
light source. Alternately, one cell is flushed with ozone-free air while the
other is simultaneously flushed with sample air. This allows a correction for
changes in light intensity and potential interfering species. The TECO 49-003
has a sensitivity of <inline-formula><mml:math id="M54" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>1 <inline-formula><mml:math id="M55" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula> and a precision of 2 <inline-formula><mml:math id="M56" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula>. The
response time is on the order of 20 <inline-formula><mml:math id="M57" display="inline"><mml:mi mathvariant="normal">s</mml:mi></mml:math></inline-formula> to reach 95 % of the new
signal (TEI, 1992). In September 2010, instrument performance of the analyzer
was assessed during the SMN/WMO/GAW 4th Tropospheric Ozone Analyzer
Intercomparison at the Servicio Meteorológico Nacional, Observatorio
Central de Buenos Aires, Buenos Aires, Argentina. The instrument passed all
checks and a comparison with an ozone traveling standard of the World
Calibration Centre for Surface Ozone (WCC-Empa) confirmed the validity of the
instrument calibration (see WCC report at
<uri>http://empa.ch/documents/56101/250799/2010_BsAs_RCC-O3.pdf</uri>).</p>
      <p>In early 2013, the station was equipped with an additional instrument
measuring greenhouse gases (Picarro Inc. G2301 CRDS for <inline-formula><mml:math id="M58" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>,
<inline-formula><mml:math id="M59" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CH</mml:mi><mml:mn mathvariant="normal">4</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M60" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">CO</mml:mi></mml:mrow></mml:math></inline-formula>, and <inline-formula><mml:math id="M61" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">H</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub><mml:mi mathvariant="normal">O</mml:mi></mml:mrow></mml:math></inline-formula> analysis) and a refurbished ozone
photometer (Thermo Scientific, TE49c) using the same measurement principle as
the TECO 49, as the latter is reaching the end of its life. The two
independent ozone time series agree well. A small systematic offset has been
observed which is most likely due to different inlet heights above ground for
the two measurement systems. A short overview comparing the overlapping
measurements of the two devices is given in the Supplement (Sect. S1,
Fig. S1). Figure S7 shows the time series of meteorological parameters.</p>
</sec>
<sec id="Ch1.S3.SS2">
  <title>Ozone data used in this study</title>
      <p>In situ ozone data from other surface stations in the GAW network (K-puszta
(Hungary), Ushuaia (USH, Argentina), Cape Point (CPT, South Africa), Cape
Grim (CGO, Australia), and La Quiaca (LQO, Argentina); see
<uri>https://gawsis.meteoswiss.ch</uri> for more details) were downloaded from the
WDCGG (<uri>http://ds.data.jma.go.jp/gmd/wdcgg/</uri>) and are used for comparison
purposes.</p>
      <p>In addition to the surface ozone measurements, ozone sondes are recording
valuable information about the vertical ozone distribution in the atmosphere,
e.g., within the SHADOZ project since 1998 (Thompson et al., 2007). Frequent
data are available from Ascension Island (United Kingdom), Suva (Fiji),
Watukosek (Java), Natal (Brazil), La Réunion (France), Pago Pago
(American Samoa), San Cristobal (Ecuador), and Irene (South Africa), where
sondes have been launched every 2 to 6 days. Additionally, ozone soundings
from Easter Island (Rapa Nui, Chile) have been kindly provided by the DMC
(P. Velázquez, personal communication, 2016) as the long-term data were
not available from any data center yet. The ozone sondes are all equipped
with an electrochemical concentration cell (ECC). According to Thompson
(2003) the agreement between the sonde and the ground-based measurements lies
around 2–7 %.</p>
      <p>Model data from two sources are used in this work to study the atmospheric
large-scale influences on the local measurements at TLL: (i) an STE
climatology from Škerlak et al. (2014) and (ii) wind field climatologies
from the ERAI. The STE climatology allows identifying the footprint of a
potential ozone contribution from the stratosphere, while the ERAI is used to
help understanding the effect of climatic variability associated, for
example, with ENSO.</p>
</sec>
<sec id="Ch1.S3.SS3">
  <title>Methods</title>
      <p>Prior to the long-term trend analysis, data are rigorously screened to
eliminate all data potentially influenced by local pollution. In a first
step, values above 55 <inline-formula><mml:math id="M62" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula> or below 10 <inline-formula><mml:math id="M63" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula> are flagged and
visually inspected for outliers, as those data points mostly arise from
zero/span checks or local influences (Fig. S2a). In a second step, a further
filtering is applied inspired by the well-established approach from Thoning
et al. (1989) applied to the long-term <inline-formula><mml:math id="M64" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> record at Mauna Loa,
Hawaii. Adapting their method to ozone and to the conditions at El Tololo,
data points with ozone mole fractions experiencing a change of more than
4 <inline-formula><mml:math id="M65" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula> from one hour to the next are excluded (Fig. S2b). This value
of 4 <inline-formula><mml:math id="M66" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula> has been defined as such to avoid too many false positives
or negatives during the automatic filtering process in order to minimize the
workload during the manual dataset review process. In a third step, a
polynomial fit is applied to the nocturnal data (23:00–06:00 LT) and data
points exceeding twice the standard deviation of all data points of the
nocturnal fit computed over one night are excluded (Fig. S2c and d). An
example of the effects of this filtering can be seen in the Supplement,
Sect. S2. A final visual inspection is performed in order to exclude any
periods of sampling problems or local pollution events referenced in the
station log books (see Table S1). As well, correction of “false negatives”
flagged by the automatic filtering routine can be recovered. Only then are
the 15-minute ambient air data averaged to hourly data, hourly averages to
daily data, and daily averages to monthly data. The filtering excludes
approximately 4.9 % of the available data, indicating the pristine
setting of the sampling site with hardly any influence from local pollution
sources from the premises' infrastructure.</p>
      <p>Trends are computed from filtered, deseasonalized monthly averages.
Deseasonalization is done using an additive model (Kendall and Stuart, 1983),
separating the seasonal component and the trend from the time series.
Significance is estimated by means of a two-sided Student <inline-formula><mml:math id="M67" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> test at the
5 % significance level except where explicitly noted. In order to make
the analysis more robust, all-time (24 <inline-formula><mml:math id="M68" display="inline"><mml:mi mathvariant="normal">h</mml:mi></mml:math></inline-formula>), nighttime (22–04 LT), and
daytime (11–17 LT) data are analyzed separately. To discern changes in the
diurnal and annual cycle, seasonal and monthly means based on hourly data of
two periods (1996–2000 and 2011–2015) are computed. Correlation tests are
assessed with the Pearson's product moment correlation coefficient, which
follows a <inline-formula><mml:math id="M69" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> distribution.</p>
      <p>To discern changes in the annual cycle, daily data have also been
investigated. The Huang–Hilbert transform technique was selected to
decompose those daily data into intrinsic mode functions (IMF) with the use
of ensemble empirical mode decomposition (EEMD; Huang and Wu, 2008; Wu and
Huang, 2009). The EEMD allows decomposition of the time series into a residual
trend and various oscillating signals representative of variations at
seasonal, synoptic, and other timescales. EEMD turned out to be particularly
powerful for this time series analysis as it succeeds to mimic the asymmetric
seasonal cycle peaking in October (see later), which is rather hard to match
with sine-curve fitting. However, EEMD is not a very suitable tool for
discontinuous time series (Barnhart et al., 2011), making it less potent when
trying to investigate particular seasons individually.</p>
      <p>Datasets of daily averages from the other GAW stations do not undergo the
filtering process. However, in order to distinguish more easily the time at
which seasonal maximum ozone mole fractions occur, a running mean with a
window of 4 days is applied to the data, including those of TLL.</p>
      <p>Ozone sounding data (see Sect. 3.2) were cumulated per station in order to get
annual cycles as follows: for each station, all soundings with valid data
were temporally aligned in order to reach data densities of as many days per
year as possible, thus creating a small climatology. Multiple values for the
same day of the year were averaged. Stations with less than 70 % data
coverage in a given year were rejected. Similarly to the surface stations,
the annual cycle is smoothed with a running mean (width of filter: soundings
with visually homogeneous, regular seasonal cycle of 10 days; soundings
with visually irregular seasonal cycles (Macquarie island, Marambio, and
Ushuaia) of 20 days) at pressure levels of 1000, 900, 800, 700, 600, and
500 <inline-formula><mml:math id="M70" display="inline"><mml:mi mathvariant="normal">hPa</mml:mi></mml:math></inline-formula> in order to compute the timing of the seasonal ozone maximum
for several altitudes.</p>
      <p>The dataset used for large-scale stratosphere-to-troposphere ozone transport
studies (Škerlak et al., 2014) is based on the ERAI data from ECMWF
(Simmons et al., 2007). Driven by the wind field of ERAI, Škerlak et
al. (2014) calculated kinematic trajectories using a three-step iterative
Eulerian integration scheme (Sprenger and Wernli, 2015). Trajectories are
started on a dense global grid and calculated for 24 <inline-formula><mml:math id="M71" display="inline"><mml:mi mathvariant="normal">h</mml:mi></mml:math></inline-formula>, where only
the ones crossing the tropopause are flagged. These flagged trajectories are
extended 4 days backward and forward, and those with a residence time in the
troposphere shorter than 48 <inline-formula><mml:math id="M72" display="inline"><mml:mi mathvariant="normal">h</mml:mi></mml:math></inline-formula> are excluded from the climatology.
Škerlak et al. (2014) estimated a transport of <inline-formula><mml:math id="M73" display="inline"><mml:mrow><mml:mn mathvariant="normal">6.52</mml:mn><mml:mo>×</mml:mo><mml:msup><mml:mn mathvariant="normal">10</mml:mn><mml:mn mathvariant="normal">11</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M74" display="inline"><mml:mi mathvariant="normal">kg</mml:mi></mml:math></inline-formula> of ozone per trajectory (<inline-formula><mml:math id="M75" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>m</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>), which is
given by the size of the model grid cell. The mass flux
(<inline-formula><mml:math id="M76" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mtext>MF</mml:mtext><mml:mrow class="chem"><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>) is then a multiplication of the number of
trajectories (<inline-formula><mml:math id="M77" display="inline"><mml:mi>n</mml:mi></mml:math></inline-formula>) per unit of time (<inline-formula><mml:math id="M78" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula>) times the mass of ozone transported
downwards through a certain model level surface (<inline-formula><mml:math id="M79" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>m</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>):

                <disp-formula id="Ch1.Ex1"><mml:math id="M80" display="block"><mml:mrow><mml:mstyle class="stylechange" displaystyle="true"/><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mtext>MF</mml:mtext><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:msub><mml:mo>≈</mml:mo><mml:mi>n</mml:mi><mml:mo>⋅</mml:mo><mml:mi>t</mml:mi><mml:mo>⋅</mml:mo><mml:mi mathvariant="normal">Δ</mml:mi><mml:msub><mml:mi>m</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:msub><mml:mo>.</mml:mo></mml:mrow></mml:math></disp-formula>

          For example, mass fluxes around TLL (see Fig. S8) amount to
8–10 <inline-formula><mml:math id="M81" display="inline"><mml:mrow><mml:mi mathvariant="normal">kg</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mo>(</mml:mo><mml:msup><mml:mi mathvariant="normal">km</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mi mathvariant="normal">s</mml:mi><mml:msup><mml:mo>)</mml:mo><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>; for comparison, the half-morning production
of ozone over the whole city of Santiago de Chile (641 <inline-formula><mml:math id="M82" display="inline"><mml:mrow><mml:msup><mml:mi mathvariant="normal">km</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>) on a
summer day amounts to around 6680 <inline-formula><mml:math id="M83" display="inline"><mml:mrow><mml:mi mathvariant="normal">kg</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mo>(</mml:mo><mml:mn mathvariant="normal">3</mml:mn><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="normal">h</mml:mi><mml:msup><mml:mo>)</mml:mo><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula> (Elshorbany et
al., 2009).</p>
</sec>
</sec>
<sec id="Ch1.S4">
  <title>Results and discussion</title>
      <p>The complete available ozone dataset at TLL from 1996 to 2015 is shown in
Fig. 4a. There are only a few extended data gaps, which are all documented in
the station log book (see Supplement, Table S1). The overall data
availability is 87 %.</p>
<sec id="Ch1.S4.SS1">
  <title>Long-term trend analysis</title>
      <p>Time series of the filtered deseasonalized monthly means is shown in Fig. 4b.
A highly significant increase of 0.66 <inline-formula><mml:math id="M84" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula> is found for
the entire period from 1996 to 2015 (<inline-formula><mml:math id="M85" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value 0.0008). The variability of
the filtered deseasonalized monthly means is within <inline-formula><mml:math id="M86" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>8 <inline-formula><mml:math id="M87" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula>.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F4"><caption><p>Time series of <bold>(a)</bold> hourly ozone mole fractions at TLL
(black) and data gaps (grey) and <bold>(b)</bold> deseasonalized monthly means of
ozone mole fractions at TLL (blue) with linear fit (red). Slope of the linear
fit is 0.66 <inline-formula><mml:math id="M88" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>; <bold>(c)</bold> residual trend of the EEMD
decomposition.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f04.pdf"/>

        </fig>

      <p>The deseasonalized ozone time series can be further decomposed using the
Huang–Hilbert transform technique. By analyzing the residual, a flattening
and a reversal of the trend are observed since 2008 and 2010, respectively
(Fig. 4c). Up to September 2010, the EEMD calculation reveals a positive
linear trend of 0.67 <inline-formula><mml:math id="M89" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>, which is in accord to the
linear fit. The EEMD calculation reverses after September 2010, resulting in
a negative trend of <inline-formula><mml:math id="M90" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>0.41 <inline-formula><mml:math id="M91" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>. Long-term trends
similar to TLL can also be found at other stations in both the SH and the NH.
Perennial trend analysis can be found in the literature, e.g., for Cape
Point, Mace Head, Cape Grim, Mauna Loa, and western US regions (e.g.,
Yellowstone National Park, Lassen, and others), and most of them show a
distinct increase in ozone mixing ratios up to the millennial years – though
mostly larger than at TLL – before showing signs of leveling off (GAW, 2013;
Carslaw, 2005; Derwent et al., 2013, 2007; Oltmans et al., 2013; Cooper et
al., 2014; Baylon et al., 2015; Lin et al., 2014). This phenomenon is
particularly pronounced at certain NH stations in Europe and in the western
US, as shown in Cooper et al. (2014): global ozone concentrations which have
been rising for more than 20 years tend to level off and even reverse quite
significantly in those regions since the millennial change. This is primarily
due to large-scale changes in <inline-formula><mml:math id="M92" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M93" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula> and VOC emissions. In contrast,
some western US stations still show signs of growing ozone concentrations, as
they are downwind of pollutants from eastern Asia. Those stations, including
Mauna Loa (Hawaii), which sample air with origin over the Pacific Ocean, may
be partly comparable with the TLL station, which is also sampling air from
oceanic origin, although the emissions of pollutants upwind of the western US
coast are by far much higher than the emissions at similar longitudes from
southern hemispheric regions (e.g., Janssens-Maenhout et al., 2015). NH
emissions are moreover prevalent over the whole year (industrial, coal
mining, and energy production being the greatest sources) compared to those
of the SH, which can be classified as seasonal peaks from biomass burning,
originating in Southeast Asia. Considering, however, the influence of ENSO on
the ozone time series (see Sect. 4.3), we conclude that air at TLL is
certainly influenced at least by a fraction by air masses originating in
Southeast Asia and Australia.</p>
      <p>Next, the ozone data from TLL will be discussed jointly with data from other
stations before the influence of large-scale phenomena is discussed in
Sect. 4.3.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F5"><caption><p><bold>(a)</bold> Mean annual cycle of ozone anomalies at different
background stations showing a spring maximum (El Tololo, TLL; La Quiaca, LQO;
Mauna Loa, MLO), a summer maximum (K-puszta, KPS), or a summer minimum (Cape
Point, CPT). Anomalies are deviations from the annual mean. The <inline-formula><mml:math id="M94" display="inline"><mml:mi>x</mml:mi></mml:math></inline-formula> axis
shows the season of the year. Northern hemispheric data are
shifted by 182 days. <bold>(b)</bold> Sine fit to the annual cycles shown
in <bold>(a)</bold>.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f05.pdf"/>

        </fig>

</sec>
<sec id="Ch1.S4.SS2">
  <?xmltex \opttitle{Annual cycles of {$\chem{O_{3}}$} at El Tololo, other ground-based sites, and from
ozone sondes}?><title>Annual cycles of <inline-formula><mml:math id="M95" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> at El Tololo, other ground-based sites, and from
ozone sondes</title>
      <p>In the following, the ozone data from TLL and other remote sites will be
discussed with respect to the time of the ozone maximum during the year as
well as the shape and the amplitude of the annual cycle.</p>
      <p>Next to TLL, different monitoring stations in the NH (Jungfraujoch (JFJ),
MLO, KPS, Payerne (PAY), and Vindeln (VDL)) and in the SH (Arrival Heights
(ARH), Baring Head (BHD), CPT, CGO, USH, and LQO) were analyzed for
comparison. Typical averaged annual cycles of selected available data
(reduced to five typical cycles with KPS (summer maximum), TLL, LQO, and MLO
(spring maximum), and CPT (winter maximum) for more clarity) are illustrated
in Fig. 5a and b, where the annual cycle of NH stations has been shifted by
182 days for comparability purposes to align the seasons for both NH and SH
stations.</p>
      <p>In order to characterize TLL as a certain type of station, a clustering of
the 10 stations into characteristic annual cycle categories has first to be
done. All investigated ground-based in situ ozone measurements  show a
maximum in either winter, spring, or summer, mainly for the three following
reasons.
(i) Winter maxima can be mainly seen in clean marine environments which are
primarily driven by ozone depletion due to negative <inline-formula><mml:math id="M96" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M97" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula> anomalies
and methyl iodide production in summer (Combrink et al., 1995; or
Nzotungicimpaye et al., 2014). (ii) Spring maxima are mainly influenced by
STE of ozone-rich air, influencing the regional chemical composition of air
through dynamic forcing. (iii) Summer maxima are mainly observed at stations
influenced by ozone precursor emissions where photochemical production of
ozone is the major process driving the annual ozone cycle.</p>
      <p>TLL stands as a good example of a station featuring a spring maximum. An
in-depth analysis of the drivers for this maximum is given below.</p>
      <p>Photochemical ozone production is mainly following the sine-shaped
availability of solar radiation, unless there is a strong seasonal variation
in the precursors, e.g., due to biomass burning emissions. Dynamic processes
such as the north–south movement of the intertropical convergence zone
(ITCZ), shifts in synoptic weather patterns, and ozone entrainment by STE can
result in less regular patterns, as the time of occurrence of the processes
is usually concentrated over a shorter time period. The STE effect at TLL,
visible in Fig. S9, smoothly starts in June, reaches a peak in August, and
regresses until December, staying at low levels until May. Little to no STE
influence is to be expected during the 5 months between January and May (see
also Sect. 4.3). This is the reason why ozone concentrations at TLL follow a
slightly asymmetric course over the year. Hence, in order to understand the
annual cycles of ozone “in three dimensions” at different latitudes in the
SH, additional data are needed.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F6"><caption><p>Composite plot showing the different southern hemispheric ozone
measurements (SHADOZ and WOUDC network and ground-based in situ data): the
<inline-formula><mml:math id="M98" display="inline"><mml:mi>x</mml:mi></mml:math></inline-formula> axis shows the southern latitude and the <inline-formula><mml:math id="M99" display="inline"><mml:mi>y</mml:mi></mml:math></inline-formula> axis represents the delta
between the maximum and the minimum of the annual cycle (“peak-to-peak
amplitude”). The size of the points represents the height of the station
(ground based) or of the ozone sonde measurement (SHADOZ and WOUDC). The
colors depict the day of year when the maximum of the annual cycle is
reached. Points with a black spot illustrate sonde measurements. TLL can be
seen at 30<inline-formula><mml:math id="M100" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> S and an amplitude of 15 <inline-formula><mml:math id="M101" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula>.</p></caption>
          <?xmltex \igopts{width=236.157874pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f06.pdf"/>

        </fig>

      <p>Therefore, ozone soundings from 12 SH remote locations (San Cristobal (SCR), Natal (NTL),
Java (JVA), Ascension Island (ASC), Samoa (SMA), Fiji (FJI), La Réunion (RNO), Irene (IRN), Rapa Nui (RAP),
Macquarie Islands (MAQ), Ushuaia (UHA), and Marambio (MAR)) have been analyzed. In Fig. 6, a compilation of our analysis of
both soundings and ground measurements is illustrated on an <inline-formula><mml:math id="M102" display="inline"><mml:mi>x</mml:mi></mml:math></inline-formula>–<inline-formula><mml:math id="M103" display="inline"><mml:mi>y</mml:mi></mml:math></inline-formula> diagram.</p>
      <p>Ozone maxima are generally shifting to later times in the year with
increasing altitude; i.e., peaks in the annual cycle at 500 <inline-formula><mml:math id="M104" display="inline"><mml:mi mathvariant="normal">hPa</mml:mi></mml:math></inline-formula> occur
later than the peaks in the annual cycle at 1000 <inline-formula><mml:math id="M105" display="inline"><mml:mi mathvariant="normal">hPa</mml:mi></mml:math></inline-formula> (see Fig. 6).
This can to a great extent be explained by the location of the soundings,
which are all launched in a marine environment. As we have learned before, in
most marine surface ozone time series a winter maximum prevails (around the
days of the year 180–220). An ascending
sounding will first sample air that is influenced by photochemistry in the
marine boundary layer. Thus, the higher a station is above sea level, the
larger is the share of stratospheric input of ozone. At high altitudes, peak
concentrations of ozone are therefore shifted towards later in the year.
However, this picture is perturbed by the fact that (i) north of
25<inline-formula><mml:math id="M106" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> S, little to no STE occurs, and (ii) the solar cycle is weak
north of 10<inline-formula><mml:math id="M107" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> S. There, interhemispheric mixing explains the late
maximum. This process allows some of the NH pollutants to penetrate into the
SH across the ITCZ. The ITCZ is also located in a region where biomass
burning prevails all year long, leading to a very efficient upward transport
of pollutants up to the tropopause. Following the position of the ITCZ, the
most intense ozone production via the <inline-formula><mml:math id="M108" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M109" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>–<inline-formula><mml:math id="M110" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">HO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M111" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>–VOC
cycle occurs late in the year. Therefore, we would expect that the maximum
shifts from a summer maximum at the equator to a spring maximum at high
latitudes.</p>
      <p>This hypothesis is further supported by a majority of the soundings (see
Fig. 6). Especially for soundings made from 25<inline-formula><mml:math id="M112" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> S southward down to
the polar regions, a clear gradient from late maxima to earlier maxima is
recognizable (shift from darker to brighter blues). This observation applies
not only to soundings but also to ground-based measurements. A trend to
earlier maxima is observed from LQO to ARH, although a smoother grading (more
stations) would be beneficial to solidify our hypothesis. When classifying
TLL, which reaches maximum values around mid-October, it can be noticed
that the timing is a bit later than one would expect from extrapolating the
ozone sonde measurements, as it is a continental station. Maximum
concentrations at CPT, CGO, BRH, USH, or ARH are reached far earlier, mainly
due to (i) the marine influence at the stations and (ii) the lack of
stratospheric influence down to the surface.</p>
      <p>The annual cycle at TLL can best be compared to sonde data taken at similar
latitude and height. This is fulfilled best by RNO and FJI. A
far weaker peak-to-peak amplitude is found at the surface station
TLL (see Fig. 6) than in the free
atmosphere. Part of this difference can be explained by the origin of air
masses, which is dynamically driven. Focusing on the soundings at Rapa Nui
(RAP), during the summer and fall months, a strong high-pressure system with
center over the island limits the advection of pollutants from the west,
hindering photochemical production of ozone. Later in the season, the
high-pressure system moves slightly eastward, allowing transport of air
masses from the northwest (Oceania) towards the southern Pacific and,
therefore, advecting biomass burning pollutants from Southeast Asia and
Oceania via the zonal wind field. In contrast, the sampled air mass at TLL is
to a greater part pristine (see above), preventing strong photolytic ozone
production in summer.</p>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T1" specific-use="star"><caption><p>Seasonal linear trends of ozone (<inline-formula><mml:math id="M113" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) at TLL for
(a) all-day data (00:00–24:00 UTC), (b) nighttime data from 22:00 to 04:00, and
(c) daytime data from 11:00 to 17:00. Significant trends are labeled with
<inline-formula><mml:math id="M114" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">a</mml:mi></mml:msup></mml:math></inline-formula> (95 %) or <inline-formula><mml:math id="M115" display="inline"><mml:msup><mml:mi/><mml:mi mathvariant="normal">b</mml:mi></mml:msup></mml:math></inline-formula> (90 %), and standard error is shown
as <inline-formula><mml:math id="M116" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>.</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="9">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="right"/>
     <oasis:colspec colnum="3" colname="col3" align="right"/>
     <oasis:colspec colnum="4" colname="col4" align="right"/>
     <oasis:colspec colnum="5" colname="col5" align="right"/>
     <oasis:colspec colnum="6" colname="col6" align="right"/>
     <oasis:colspec colnum="7" colname="col7" align="right"/>
     <oasis:colspec colnum="8" colname="col8" align="right"/>
     <oasis:colspec colnum="9" colname="col9" align="right"/>
     <oasis:thead>
       <oasis:row rowsep="1">  
         <oasis:entry colname="col1">Time of day/season</oasis:entry>  
         <oasis:entry colname="col2">DJF</oasis:entry>  
         <oasis:entry colname="col3"><inline-formula><mml:math id="M117" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value</oasis:entry>  
         <oasis:entry colname="col4">MAM</oasis:entry>  
         <oasis:entry colname="col5"><inline-formula><mml:math id="M118" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value</oasis:entry>  
         <oasis:entry colname="col6">JJA</oasis:entry>  
         <oasis:entry colname="col7"><inline-formula><mml:math id="M119" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value</oasis:entry>  
         <oasis:entry colname="col8">SON</oasis:entry>  
         <oasis:entry colname="col9"><inline-formula><mml:math id="M120" display="inline"><mml:mi>p</mml:mi></mml:math></inline-formula> value</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>  
         <oasis:entry colname="col1">All</oasis:entry>  
         <oasis:entry colname="col2"><inline-formula><mml:math id="M121" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>0.1 <inline-formula><mml:math id="M122" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 0.05</oasis:entry>  
         <oasis:entry colname="col3">0.619</oasis:entry>  
         <oasis:entry colname="col4"><inline-formula><mml:math id="M123" display="inline"><mml:mrow><mml:msup><mml:mn mathvariant="normal">1.6</mml:mn><mml:mi mathvariant="normal">a</mml:mi></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.06</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col5">0.0353</oasis:entry>  
         <oasis:entry colname="col6"><inline-formula><mml:math id="M124" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.2</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.04</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col7">0.855</oasis:entry>  
         <oasis:entry colname="col8"><inline-formula><mml:math id="M125" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.1</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.07</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col9">0.881</oasis:entry>
       </oasis:row>
       <oasis:row>  
         <oasis:entry colname="col1">Nighttime</oasis:entry>  
         <oasis:entry colname="col2"><inline-formula><mml:math id="M126" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.03</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.06</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col3">0.843</oasis:entry>  
         <oasis:entry colname="col4"><inline-formula><mml:math id="M127" display="inline"><mml:mrow><mml:msup><mml:mn mathvariant="normal">1.8</mml:mn><mml:mi mathvariant="normal">a</mml:mi></mml:msup><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.07</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col5">0.0271</oasis:entry>  
         <oasis:entry colname="col6"><inline-formula><mml:math id="M128" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.3</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.04</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col7">0.745</oasis:entry>  
         <oasis:entry colname="col8"><inline-formula><mml:math id="M129" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.1</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.07</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col9">0.821</oasis:entry>
       </oasis:row>
       <oasis:row>  
         <oasis:entry colname="col1">Daytime</oasis:entry>  
         <oasis:entry colname="col2"><inline-formula><mml:math id="M130" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>0.4 <inline-formula><mml:math id="M131" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 0.05</oasis:entry>  
         <oasis:entry colname="col3">0.231</oasis:entry>  
         <oasis:entry colname="col4"><inline-formula><mml:math id="M132" display="inline"><mml:mrow><mml:msup><mml:mn mathvariant="normal">1.2</mml:mn><mml:mi mathvariant="normal">b</mml:mi></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.06</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col5">0.0909</oasis:entry>  
         <oasis:entry colname="col6"><inline-formula><mml:math id="M133" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.1</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.01</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col7">0.866</oasis:entry>  
         <oasis:entry colname="col8"><inline-formula><mml:math id="M134" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.1</mml:mn><mml:mo>±</mml:mo><mml:mn mathvariant="normal">0.06</mml:mn></mml:mrow></mml:math></inline-formula></oasis:entry>  
         <oasis:entry colname="col9">0.802</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

</sec>
<sec id="Ch1.S4.SS3">
  <title>Large-scale influences at TLL</title>
      <p>There are several large-scale processes which potentially impact either
short-term or long-term ozone variations at TLL. These factors include
large-scale advection of air masses either via the subtropical jet or via
potential vorticity cutoffs from the polar jet region,
STE of ozone-rich air from the stratosphere,
as well as pattern changes in tropical up- or downwelling. The impact of
these different elements not only vary over the course of a day (storm-scale)
or of a year (seasonal cycles) but may also oscillate over timescales of 2
to 7 years, following teleconnections and large-scale oscillations from
features like the quasi-biennial oscillation (QBO) or ENSO.</p>
      <p>All these influences are visible in the different ozone data products from
TLL. We initially focus on the changes in the mean annual cycle of ozone over
time and, based on this, elaborate further on the timing of the maximum and
on the shape of the cycle. We conclude this section with a short overview of
the observed short-term variations (week scale) including a possible
interpretation for those findings.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F7"><caption><p>Mean annual cycles of ozone mole fraction (1996–2000 and
2011–2015) showing mean, upper 95th percentile, and lower 5th percentile. For
better readability, the monthly means for both periods have been shifted by
<inline-formula><mml:math id="M135" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>6 days.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f07.pdf"/>

        </fig>

      <?xmltex \floatpos{t}?><fig id="Ch1.F8"><caption><p>Mean annual cycle over 19 years (1996–2015) of ozone at TLL and of
trajectories indicating STE above TLL. For better readability, the monthly
means for both variables have been shifted by
<inline-formula><mml:math id="M136" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula>6 days.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f08.pdf"/>

        </fig>

      <p>First, two mean seasonal cycles for two 5-year periods, one at the beginning
of the measurements (1996–2000) and the other one in the recent past
(2011–2015), were analyzed for potential differences. In Fig. 7, the monthly
means, with the upper 95th and the lower 5th percentiles including associated
uncertainties, are presented. Table 1 summarizes the findings in numbers. The
two periods show a very similar annual cycle. However, there are subtle
differences: especially in austral fall (February–March), the 5th
percentile, mean, and  95th percentile increased remarkably from the first
to the second period. Among the three curves, the 5th percentile shows the
most persistent increase from February up to June in the more recent period.
For the other months of the year, changes are minor except for October, where
2011–2015 show slightly lower values of <inline-formula><mml:math id="M137" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>. The annual cycle and
some of the differences between the two periods are mainly driven by the
annual cycle of ozone-STE mass flux (see Figs. 8 and S9). However, the
increase of ozone mole fractions from March to May cannot be explained by STE
only, as at that time ozone-STE mass flux shows negative anomalies
(Fig. S9). Here, three other factors, like QBO or ENSO, change in large-scale
dynamics and precursor species have to be taken into account.
<list list-type="custom"><list-item><label>i.</label>
      <p>As Neu et al. (2014) showed, positive QBO shear and the multivariate
ENSO index (MEI) lead to increased stratospheric air circulation, negative
upper troposphere ozone anomalies (due to upwelling of relatively
ozone-depleted air), and therefore potentially decreased ozone-STE activity
in the sub- and extratropics. Doherty et al. (2006) and Sekiya and Sudo
(2012) explained the decrease in total column ozone found in the eastern
Pacific region during El Niño conditions with a decrease in <inline-formula><mml:math id="M138" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M139" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>
production due to a decrease in lightning activity. The ozone anomalies at
TLL and the MEI show significant correlations especially in
September–October (correlation of <inline-formula><mml:math id="M140" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>0.78), and the annual cycles of ozone
during El Niño years and La Niña years indeed show significantly
different values especially in austral fall and spring (Fig. 10). During La
Niña events, ozone levels reach higher values – especially from
September to November – than during El Niño events. Figure S10
illustrates that the 1996–2000 period not only had a weak positive
correlation (correlation of 0.28) of both (QBO shear/ME) indexes but also had one single
strong El Niño event lasting nearly 2 years, possibly leading to a
decreased ozone-STE burden in 1997–1998. The second, later period showed
nearly no in-phase correlation of MEI and QBO shear index (correlation of
<inline-formula><mml:math id="M141" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>0.04) and no significant El Niño event.</p></list-item><list-item><label>ii.</label>
      <p>The subtropical jet
has to be considered as contributing factor to the MAM anomaly in the
2011–2015 period. We assume that with the broadening of the Hadley cell (HC;
Choi et al., 2014; Nguyen et al., 2013), the extratropical jet, moving to
higher latitudes, increasingly advected more polluted air from Southeast
Asia, e.g., in the form of peroxyacetyl nitrate (PAN; Jiang et al., 2016), during
this period of the year, when biomass burning prevails (e.g., Streets et
al., 2003). More work has to be done to confirm this theory, e.g., using
satellite measurements, as this would go beyond the scope of this work.</p></list-item><list-item><label>iii.</label>
      <p>An increase of biomass burning in Southeast Asia (e.g., Shi and
Yamaguchi, 2014; Verma et al., 2015) and Australia (Cooper et al., 2014) with
subsequent eastward transport of ozone precursors could also explain the
positive anomaly in MAM in the 2011–2015 period, as the northward migration
of the ITCZ during this time of the year starts to allow effects of NH
emissions to be seen in the SH and prevailing westerly conditions (see
Fig. 2) exclude any sensitivity of ozone mole fractions at TLL to emissions
on the South American continent. At most, the ozone increase may originate
from regional pollution from the La Serena region, which – in fall – may
get transported upwards due to the PBL height and occasional support by
frontal systems. This latter assumption remains, however, hypothetical. A
confirmation would require high-resolution numerical simulations to resolve
the transport in the mountainous terrain of TLL.</p></list-item></list></p>
      <p>In summary, we conclude that the annual cycle is mostly driven by STE from
June to January. From February to April, however, the broadening of the HC
with subsequent transport of pollutants from Southeast Asia, the contrast to
El Niño dominated (1996–2000) versus average years (2011–2015), and the
increase in precursor species in Southeast Asia are the best explanations for
the positive ozone anomaly in the more recent period. From Table 1, we
conclude furthermore that, in general, differences between nighttime and
daytime trends are very low, which indicates that TLL is a very good
background station with similar ozone levels under free-tropospheric
conditions and under planetary boundary layer (PBL) influence. Mean ozone
mole fractions at TLL only vary between 32.5 and 31.0 <inline-formula><mml:math id="M142" display="inline"><mml:mi mathvariant="normal">ppb</mml:mi></mml:math></inline-formula> during day
and night, while other stations located near greater cities (e.g., eastern
US; Bloomer et al., 2010) report up to 50 ppb peak differences between
nighttime and daytime. This finding is most probably attributed not only to
the remote location, far away from pollutant sources, but also to the high
altitude located above the PBL.</p>
      <p>Regarding the 2-month lag between the recent maximum of STE ozone mass flux
and the recent maximum of ozone mixing ratio in Figs. 7 vs. S9, we explain
this delayed response of ozone to STE by the following mechanisms:
(i) a certain amount of time is needed to equally distribute ozone stemming
from STE in the lower troposphere (e.g., titration of <inline-formula><mml:math id="M143" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M144" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula> and
<inline-formula><mml:math id="M145" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">HO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M146" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula> residing in the atmosphere) in order to reach chemical
equilibrium; and (ii) deep convection underestimation as well as seasonal
cycle uncertainties within the ERAI dataset (Škerlak et al., 2014) lead
to doubts concerning the exact onset of ozone-STE mass flux maximum around
the cordillera.</p>
      <p>Concerning the timing of the maximum, Fig. 8 shows a strong correlation
(correlation of 0.89) between
the mean annual cycle of STE trajectories (Škerlak, 2014) and of the
ozone concentration. The two parameters show a strikingly similar pattern,
indicating that STE may be a strong driver for <inline-formula><mml:math id="M147" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>. Note that the
“mass flux into the PBL” illustrated in Fig. S9 shows a slightly earlier
peak occurrence than the number of “STE trajectories”. Another indication
for the coupling of <inline-formula><mml:math id="M148" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> concentration and STE is a coherent shift in
the maximum of these quantities over the observation period towards an
earlier occurrence in the year. This is illustrated in Fig. 9. For
calculation, a 4-year sliding window of daily data was defined and run over
all data between 1996 and 2015. Then, an empirical mode decomposition was
done (Huang and Wu, 2008; Wu and Huang, 2009). Out of the Hilbert
periodogram, the IMF resembling the most to an annual cycle is selected and
the IMF data points are extracted. The latter are averaged to get an average
of IMF over the 4-year window. Finally, the day-of-year matching the maximum
value of the IMF is extracted. For the ozone time series, a regression of
<inline-formula><mml:math id="M149" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>10 days per decade was calculated. For STT, an even larger trend of <inline-formula><mml:math id="M150" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>11
or <inline-formula><mml:math id="M151" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>21 days per decade was obtained for the maximum number of trajectories
of stratospheric origin and for the mass flux into the PBL, respectively.
Note that the regression is only poorly visible in Fig. 7, where data are
aggregated in monthly bins and a comparison of three different percentiles of
5-year monthly averages, instead of absolute maximal values, is shown.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F9"><caption><p>Time of  year for which the maximum of ozone (red), STE
trajectories (blue), and STE mass flux into the PBL (green) are reached. A
4-year sliding window of daily data was applied. Average values for the years
1996–1999 are shown as the data point at the end of December 1997, 1997–2000 at the
end of December 1998, and so forth, until years 2012–2015, which are shown as
data point at the end of December 2013.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f09.pdf"/>

        </fig>

      <?xmltex \floatpos{t}?><fig id="Ch1.F10"><caption><p>Computed annual cycle of <inline-formula><mml:math id="M152" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> mole fractions at TLL in daily
resolution during El Niño days (NINO3.4 Index <inline-formula><mml:math id="M153" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 0.5, total 1914 days
between December 1995 and December 2015) and La Niña days
(NINO3.4 Index <inline-formula><mml:math id="M154" display="inline"><mml:mo>&lt;</mml:mo></mml:math></inline-formula> <inline-formula><mml:math id="M155" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>0.5, total 2330 days between December 1995 and
December 2015). Black lines show significant differences between the two
curves. NINO3.4 data are derived from daily index reconstructions from SST OI
v2 <inline-formula><mml:math id="M156" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mo>/</mml:mo><mml:mn mathvariant="normal">4</mml:mn></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M157" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula> data by NOAA.</p></caption>
          <?xmltex \igopts{width=213.395669pt}?><graphic xlink:href="https://acp.copernicus.org/articles/17/6477/2017/acp-17-6477-2017-f10.pdf"/>

        </fig>

      <p>This shift in the seasonal cycle to earlier times in the year has already
been presented in other studies for other locations (Parrish et al., 2013;
Lin et al., 2014). For instance, spring peaks are observed in the NH to
regress with a rate of 3–14 days per decade (Parrish et al., 2013). Parrish
et al. (2013) also suggest that the relative contribution from the
stratosphere may at least partly explain the shift in the annual cycle at
high-altitude stations in the NH like Jungfraujoch, being located at
3580 <inline-formula><mml:math id="M158" display="inline"><mml:mi mathvariant="normal">m</mml:mi></mml:math></inline-formula> a.s.l. However, a conclusive explanation for this shift of the
seasonal cycle remains missing. Schnell et al. (2016) recently suggested that
future climate change will shift the maximum of the ozone seasonal cycle to
earlier in the year, but they did not provide any clear explanation for this
phenomenon.</p>
      <p>Considering the short-term variations, it is known from previous studies that
a (anti)correlation between ozone and relative humidity exists at TLL, but
only in very specific cases. Gallardo et al. (2000), analyzing the first
years of data collected at Tololo, found such an anticorrelation between
ozone and water vapor in summer in connection with upslope transport of
boundary layer air associated with a thermally driven circulation. Rondanelli
et al. (2002) investigated the effect of troughs associated with a frontal
zone passing over TLL and classified their observations in two
categories: wet and dry events. During wet events, relatively humid air from
the PBL is advected to TLL and, shortly after regression of relative
humidity, ozone rises rapidly. During dry events, ozone rises, but
relative humidity stays at normal, dry levels or drops even further. Carbon
monoxide, a good PBL pollutant and hence an optimal tracer, has been measured
in TLL since April 2013. Therefore, the dependence of CO and ozone was
investigated. This analysis revealed a significant correlation (not shown) in
rare, specific episodes, during which less-pristine air from the PBL –
originating from the La Serena, Valparaíso, and Santiago regions – reaches TLL. Those events were not always associated with low potential
vorticity values (PV streamer, reconstructed from ERAI data, not
shown) or frontal zones, but some of them were. This confirms the finding of
Rutllant et al. (2013), who, during the VOCALS-REx campaign, found a
persistent, regular southwesterly advection via thermals,  able to
transport air masses in the afternoon from the marine region into the Andes,
which would allow inbound transport of slightly more polluted air masses to
TLL. An in-depth analysis of <inline-formula><mml:math id="M159" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">CO</mml:mi></mml:mrow></mml:math></inline-formula>–<inline-formula><mml:math id="M160" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> correlations over several
years may be promising to provide more robust conclusions. However, the CO
time series is still limited in time and an extended study would go beyond
the scope of the paper.</p><?xmltex \hack{\newpage}?>
</sec>
</sec>
<sec id="Ch1.S5" sec-type="conclusions">
  <title>Conclusions</title>
      <p>The 20-year-long surface ozone time series of El Tololo, Chile
(TLL), has been presented and analyzed. It was characterized and put into a
global context with the help of STE
climatology, trajectory analysis, surface ozone data from other stations, as
well as ozone soundings. The analysis shows that El Tololo represents a
remote measuring site in a pristine setting, which rarely gets influenced by
local pollution, and thus represents an excellent remote GAW station. An
indication of this is the relatively small amplitude of the diurnal cycle,
even in summer.</p>
      <p>The following list summarizes the most important conclusions:
<list list-type="bullet"><list-item>
      <p>Only a few data gaps exist in the 20-year-long ozone dataset.</p></list-item><list-item>
      <p>A positive trend of <inline-formula><mml:math id="M161" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula>0.66 <inline-formula><mml:math id="M162" display="inline"><mml:mrow><mml:mi mathvariant="normal">ppb</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula> is found up to recent
years, which gets weaker from 2010 on and possibly reverses in 2011.</p></list-item><list-item>
      <p>Over the entire period, the strongest increase in ozone
concentrations is observed in austral fall and the strongest decrease in austral
summer. This most probably is related to different origins of the air masses
and to an increase in precursor species over Southeast Asia.</p></list-item><list-item>
      <p>In general, the average annual cycle at TLL is dominated by peak
concentrations in late spring, followed by a sharp decrease in late winter to
early fall, correlating with the shape of average annual STE. TLL can,
therefore, be mainly classified as a STE-influenced station, in contrast to
stations that are in the marine boundary layer or significantly influenced by
anthropogenic pollution.</p></list-item><list-item>
      <p>Characterizing the TLL dataset with the help of ozone soundings
makes it possible to see that the free-tropospheric influence is very strong
compared to other stations.</p></list-item><list-item>
      <p>The maximum ozone concentrations were reached around week 41 (early
October) in 1996 and have been retrograding since; recently, maximum
concentrations are reached around week 38 (<inline-formula><mml:math id="M163" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>10 <inline-formula><mml:math id="M164" display="inline"><mml:mrow><mml:mi mathvariant="normal">days</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>).
This is attributed to a retrogradation in the same magnitude of the maximum
in the ST mass flux into the PBL (<inline-formula><mml:math id="M165" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>21 <inline-formula><mml:math id="M166" display="inline"><mml:mrow><mml:mi mathvariant="normal">days</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>) and of the
number of STE trajectories around El Tololo
(<inline-formula><mml:math id="M167" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>11 <inline-formula><mml:math id="M168" display="inline"><mml:mrow><mml:mi mathvariant="normal">days</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">decade</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>).</p></list-item><list-item>
      <p>The ozone concentrations at El Tololo are sensitive to the ENSO. Over
the entire year, ozone concentrations are higher during La Niña
conditions than during El Niño conditions, especially in late austral
spring. This is related to large-scale atmospheric circulation anomalies over
the Pacific, changing the strength of the tropical upwelling and coming along
with less <inline-formula><mml:math id="M169" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M170" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula> production by lightning and changing circulation patterns.</p></list-item></list></p>
      <p>While many aspects of the <inline-formula><mml:math id="M171" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> time series are well explained, two
observations remain unclear and may be elucidated with the help of regional
and a global modeling studies. Firstly, the origin of the retrogradation of
the timing of ozone-STE maximum is yet unclear. Our hypothesis is that
large-scale gravity wave momentum transport has changed over years due to
changing tropopause height. Secondly, different ozone trends for different
seasons (austral fall versus austral summer) are observed. While part of it
can be explained with an increase in precursor species during the biomass
burning season over Southeast Asia, we postulate that a second explanation
that polluted air masses from the greater Santiago area are transported
northwards up to La Serena, where the local wind systems (Elqui Valley wind)
transports the plume up to El Tololo. This process has been confirmed by a
short preliminary study with a regional model. At least 1 year of
high-resolution regional model results is required to be able to confirm or
reject this hypothesis.</p>
</sec>

      
      </body>
    <back><notes notes-type="dataavailability">

      <p>The data product of El Tololo are available on the WDCGG
web page free of charge
(<uri>http://ds.data.jma.go.jp/gmd/wdcgg/cgi-bin/wdcgg/download.cgi?index=TLL330S00-DMC&amp;param=201412030001&amp;select=inventory</uri>)</p>
  </notes><app-group>
        <supplementary-material position="anchor"><p><bold>The Supplement related to this article is available online at <inline-supplementary-material xlink:href="http://dx.doi.org/10.5194/acp-17-6477-2017-supplement" xlink:title="pdf">doi:10.5194/acp-17-6477-2017-supplement</inline-supplementary-material>.</bold></p></supplementary-material>
        </app-group><notes notes-type="competinginterests">

      <p>The authors declare that they have no conflict of
interest.</p>
  </notes><ack><title>Acknowledgements</title><p>We acknowledge the support of the Federal Office of Meteorology and
Climatology MeteoSwiss through the project Capacity Building and Twinning for
Climate Observing Systems (CATCOS) Phase 2, contract no. 81025332, between
the Swiss Agency for Development and Cooperation (SDC) and MeteoSwiss.
Moreover, we would like to express our gratitude towards Michael Sprenger and
Bojan Skerlak, who both advised us how to use their ozone-STE climatology. As
well, we thank Dr. Stephan Henne for his support concerning the FLEXTRA
datasets and Dr. Dominik Brunner for his valuable comments. Laura Gallardo is
grateful for the support of FONDAP 15110009. We would also like to thank the
two anonymous reviewers and the editor, Jason West, for their detailed and
helpful comments.<?xmltex \hack{\newline}?><?xmltex \hack{\newline}?>
Edited by: J. West <?xmltex \hack{\newline}?>
Reviewed by: two anonymous referees</p></ack><?xmltex \hack{\newpage}?><?xmltex \hack{\newpage}?><ref-list>
    <title>References</title>

      <ref id="bib1.bib1"><label>1</label><mixed-citation>Ayers, G. P., Penkett, S. A., Gillet, R. W., Bandy, B., Galbally, I. E.,
Meyer, C. P., Elsworth, C. M., Bentley, S. T., and Forgan, B. W.: Evidence
for photochemical control of ozone concentrations in unpolluted marine air,
Nature, 360, 446–449, <ext-link xlink:href="http://dx.doi.org/10.1038/360446a0" ext-link-type="DOI">10.1038/360446a0</ext-link>, 1992.</mixed-citation></ref>
      <ref id="bib1.bib2"><label>2</label><mixed-citation>Barlasina, M. E., Carbajal Benitez, G., Copes, G., Demasi, M., and Cupeiro,
M.: Estudio del ozono troposférico en tres observatorios de la red de
medición del servicio meteorológico nacional – argentina,
Proceedings CONGREMET XI, Mendoza, 29 May–1 June 2012, available at:
<uri>http://www.congremet.prmarg.org/upload/barlasinamaelena.pdf</uri> (last
access: 20 May 2017), 2013.</mixed-citation></ref>
      <ref id="bib1.bib3"><label>3</label><mixed-citation>Barnhart, B. L., Nandage, H. K. W., and Eichinger, W.: Assessing
Discontinuous Data Using Ensemble Empirical Mode Decomposition, Advances in
Adaptive Data Analysis, 03, 483–491, <ext-link xlink:href="http://dx.doi.org/10.1142/s179353691100091x" ext-link-type="DOI">10.1142/s179353691100091x</ext-link>, 2011.</mixed-citation></ref>
      <ref id="bib1.bib4"><label>4</label><mixed-citation>Baylon, P., Jaffe, D. A., Wigder, N. L., Gao, H., and Hee, J.: Ozone
enhancement in western US wildfire plumes at the Mt. Bachelor Observatory:
The role of <inline-formula><mml:math id="M172" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M173" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>, Atmos. Environ., 109, 297–304,
<ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2014.09.013" ext-link-type="DOI">10.1016/j.atmosenv.2014.09.013</ext-link>, 2015.</mixed-citation></ref>
      <ref id="bib1.bib5"><label>5</label><mixed-citation>Bloomer, B. J., Vinnikov, K. Y., and Dickerson, R. R.: Changes in seasonal
and diurnal cycles of ozone and temperature in the eastern U.S, Atmos.
Environ., 44, 2543–2551, <ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2010.04.031" ext-link-type="DOI">10.1016/j.atmosenv.2010.04.031</ext-link>, 2010.</mixed-citation></ref>
      <ref id="bib1.bib6"><label>6</label><mixed-citation>Brook, R. D.: Inhalation of Fine Particulate Air Pollution and Ozone Causes
Acute Arterial Vasoconstriction in Healthy Adults, Circulation, 105,
1534–1536, <ext-link xlink:href="http://dx.doi.org/10.1161/01.CIR.0000013838.94747.64" ext-link-type="DOI">10.1161/01.CIR.0000013838.94747.64</ext-link>, 2002.</mixed-citation></ref>
      <ref id="bib1.bib7"><label>7</label><mixed-citation>Carslaw, D. C.: On the changing seasonal cycles and trends of ozone at Mace
Head, Ireland, Atmos. Chem. Phys., 5, 3441–3450,
<ext-link xlink:href="http://dx.doi.org/10.5194/acp-5-3441-2005" ext-link-type="DOI">10.5194/acp-5-3441-2005</ext-link>, 2005.</mixed-citation></ref>
      <ref id="bib1.bib8"><label>8</label><mixed-citation>Choi, J., Son, S.-W., Lu, J., and Min, S.-K.: Further observational evidence
of Hadley cell widening in the Southern Hemisphere, Geophys. Res. Lett., 41,
2590–2597, <ext-link xlink:href="http://dx.doi.org/10.1002/2014GL059426" ext-link-type="DOI">10.1002/2014GL059426</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib9"><label>9</label><mixed-citation>
Collins, W. J., Derwent, R. G., Garnier, B., Johnson, C. E., Sanderson,
M. G., and Stevenson, D. S.: Effect of stratosphere-troposphere exchange on
the future tropospheric ozone trend, J. Geophys. Res., 108, 8528,
10.1029/2002JD002617, 2003.</mixed-citation></ref>
      <ref id="bib1.bib10"><label>10</label><mixed-citation>Combrink, J., Diab, R. D., Sokolic, F., and Brunke, E. G.: Relationship
between surface, free tropospheric and total column ozone in two contrasting
areas in South Africa, Atmos. Environ., 29, 685–691,
<ext-link xlink:href="http://dx.doi.org/10.1016/1352-2310(94)00313-A" ext-link-type="DOI">10.1016/1352-2310(94)00313-A</ext-link>, 1995.</mixed-citation></ref>
      <ref id="bib1.bib11"><label>11</label><mixed-citation>Cooper, O. R., Gao, R. S., Tarasick, D., Leblanc, T., and Sweeney, C.:
Long-term ozone trends at rural ozone monitoring sites across the United
States, 1990–2010, J. Geophys. Res., 117, 1990–2010,
<ext-link xlink:href="http://dx.doi.org/10.1029/2012JD018261" ext-link-type="DOI">10.1029/2012JD018261</ext-link>, 2012.</mixed-citation></ref>
      <ref id="bib1.bib12"><label>12</label><mixed-citation>Cooper, O. R., Parrish, D. D., Ziemke, J., Balashov, N. V., Cupeiro, M.,
Galbally, I. E., Gilge, S., Horowitz, L., Jensen, N. R., Lamarque, J. F.,
Naik, V., Oltmans, S. J., Schwab, J., Shindell, D. T., Thompson, A. M.,
Thouret, V., Wang, Y., and Zbinden, R. M.: Global distribution and trends of
tropospheric ozone: An observation-based review, Elementa, 2, 000029,
<ext-link xlink:href="http://dx.doi.org/10.12952/journal.elementa.000029" ext-link-type="DOI">10.12952/journal.elementa.000029</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib13"><label>13</label><mixed-citation>Crutzen, P.: A discussion of the chemistry of some minor constituents in the
stratosphere and troposphere, Pure Appl. Geophys., 106, 1385–1399,
<ext-link xlink:href="http://dx.doi.org/10.1007/bf00881092" ext-link-type="DOI">10.1007/bf00881092</ext-link>, 1973.
</mixed-citation></ref><?xmltex \hack{\newpage}?>
      <ref id="bib1.bib14"><label>14</label><mixed-citation>Crutzen, P. J.: Ozone production rates in an oxygen-hydrogen-nitrogen oxide
atmosphere, J. Geophys. Res., 76, 7311–7311, <ext-link xlink:href="http://dx.doi.org/10.1029/JC076i030p07311" ext-link-type="DOI">10.1029/JC076i030p07311</ext-link>,
1971.</mixed-citation></ref>
      <ref id="bib1.bib15"><label>15</label><mixed-citation>Crutzen, P. J. and Zimmermann, P. H.: The changing photochemistry of the
troposphere, Tellus B, 43, 136–151,
<ext-link xlink:href="http://dx.doi.org/10.1034/j.1600-0889.1991.t01-1-00012.x" ext-link-type="DOI">10.1034/j.1600-0889.1991.t01-1-00012.x</ext-link>, 1991.</mixed-citation></ref>
      <ref id="bib1.bib16"><label>16</label><mixed-citation>Derwent, R. G., Jenkin, M. E., Saunders, S. M., and Pilling, M. J.:
Photochemical ozone creation potentials for organic compounds in northwest
Europe calculated with a master chemical mechanism, Atmos. Environ., 32,
2429–2441, <ext-link xlink:href="http://dx.doi.org/10.1016/S1352-2310(98)00053-3" ext-link-type="DOI">10.1016/S1352-2310(98)00053-3</ext-link>, 1998.</mixed-citation></ref>
      <ref id="bib1.bib17"><label>17</label><mixed-citation>Derwent, R. G., Simmonds, P. G., Manning, A. J., and Spain, T. G.: Trends
over a 20-year period from 1987 to 2007 in surface ozone at the atmospheric
research station, Mace Head, Ireland, Atmos. Environ., 41, 9091–9098,
<ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2007.08.008" ext-link-type="DOI">10.1016/j.atmosenv.2007.08.008</ext-link>, 2007.</mixed-citation></ref>
      <ref id="bib1.bib18"><label>18</label><mixed-citation>Derwent, R. G., Manning, A. J., Simmonds, P. G., Spain, T. G., and O'Doherty,
S.: Analysis and interpretation of 25 years of ozone observations at the Mace
Head Atmospheric Research Station on the Atlantic Ocean coast of Ireland from
1987 to 2012, Atmos. Environ., 80, 361–368,
<ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2013.08.003" ext-link-type="DOI">10.1016/j.atmosenv.2013.08.003</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib19"><label>19</label><mixed-citation>Doherty, R. M., Stevenson, D. S., Johnson, C. E., Collins, W. J., and
Sanderson, M. G.: Tropospheric ozone and El Niño–Southern Oscillation:
Influence of atmospheric dynamics, biomass burning emissions, and future
climate change, J. Geophys. Res., 111, D19304, <ext-link xlink:href="http://dx.doi.org/10.1029/2005JD006849" ext-link-type="DOI">10.1029/2005JD006849</ext-link>,
2006.</mixed-citation></ref>
      <ref id="bib1.bib20"><label>20</label><mixed-citation>Elshorbany, Y. F., Kleffmann, J., Kurtenbach, R., Rubio, M., Lissi, E.,
Villena, G., Gramsch, E., Rickard, A. R., Pilling, M. J., and Wiesen, P.:
Summertime photochemical ozone formation in Santiago, Chile, Atmos. Environ.,
43, 6398–6407, <ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2009.08.047" ext-link-type="DOI">10.1016/j.atmosenv.2009.08.047</ext-link>, 2009.</mixed-citation></ref>
      <ref id="bib1.bib21"><label>21</label><mixed-citation>Fiscus, E. L., Booker, F. L., and Burkey, K. O.: Crop responses to ozone:
Uptake, modes of action, carbon assimilation and partitioning, Plant Cell
Environ., 28, 997–1011, <ext-link xlink:href="http://dx.doi.org/10.1111/j.1365-3040.2005.01349.x" ext-link-type="DOI">10.1111/j.1365-3040.2005.01349.x</ext-link>, 2005.</mixed-citation></ref>
      <ref id="bib1.bib22"><label>22</label><mixed-citation>Fuenzalida, H. A., Sánchez, R., and Garreaud, R. D.: A climatology of
cutoff lows in the Southern Hemisphere, J. Geophys. Res., 110, D18101,
<ext-link xlink:href="http://dx.doi.org/10.1029/2005JD005934" ext-link-type="DOI">10.1029/2005JD005934</ext-link>, 2005.</mixed-citation></ref>
      <ref id="bib1.bib23"><label>23</label><mixed-citation>Galbally, I.: Some Measurements of Ozone Variation and Destruction in the
Atmospheric Surface Layer, Nature, 218, 456–457, <ext-link xlink:href="http://dx.doi.org/10.1038/218456a0" ext-link-type="DOI">10.1038/218456a0</ext-link>,
1968.</mixed-citation></ref>
      <ref id="bib1.bib24"><label>24</label><mixed-citation>Gallardo, L., Carrasco, J., and Olivares, G.: An analysis of ozone
measurements at Cerro Tololo (30<inline-formula><mml:math id="M174" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>S, 70<inline-formula><mml:math id="M175" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>W, 2200 m.a.s.l.) in
Chile, Tellus B, 52, 50–59, <ext-link xlink:href="http://dx.doi.org/10.1034/j.1600-0889.2000.00959.x" ext-link-type="DOI">10.1034/j.1600-0889.2000.00959.x</ext-link>, 2000.</mixed-citation></ref>
      <ref id="bib1.bib25"><label>25</label><mixed-citation>Garreaud, R. D. and Muñoz, R. C.: The Low-Level Jet off the West Coast of
Subtropical South America: Structure and Variability, Mon. Weather Rev., 133,
2246–2261, <ext-link xlink:href="http://dx.doi.org/10.1175/mwr2972.1" ext-link-type="DOI">10.1175/mwr2972.1</ext-link>, 2005.</mixed-citation></ref>
      <ref id="bib1.bib26"><label>26</label><mixed-citation>
GAW: GAW Report No. 209: Guidelines for Continuous Measurements of Ozone in
the Troposphere, WMO and GAW, WMO-No. 1110, 82 pp., 2013.</mixed-citation></ref>
      <ref id="bib1.bib27"><label>27</label><mixed-citation>Geiger, R.: Überarbeitete Neuausgabe von Geiger, R:
Köppen-Geiger/Klima der Erde, Wandkarte <inline-formula><mml:math id="M176" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mo>:</mml:mo><mml:mn mathvariant="normal">16</mml:mn></mml:mrow></mml:math></inline-formula> Mill., Klett-Perthes,
Gotha, 1961.</mixed-citation></ref>
      <ref id="bib1.bib28"><label>28</label><mixed-citation>Hegglin, M. I. and Shepherd, T. G.: Large climate-induced changes in
ultraviolet index and stratosphere-to-troposphere ozone flux, Nat. Geosci.,
2, 687–691, <ext-link xlink:href="http://dx.doi.org/10.1038/ngeo604" ext-link-type="DOI">10.1038/ngeo604</ext-link>, 2009.</mixed-citation></ref>
      <ref id="bib1.bib29"><label>29</label><mixed-citation>Holton, J. R., Haynes, P. H., McIntyre, M. E., Douglass, A. R., Rood, R. B.,
and Pfister, L.: Stratosphere–troposphere exchange, Rev. Geophys., 33,
403–403, <ext-link xlink:href="http://dx.doi.org/10.1029/95RG02097" ext-link-type="DOI">10.1029/95RG02097</ext-link>, 1995.</mixed-citation></ref>
      <ref id="bib1.bib30"><label>30</label><mixed-citation>Huang, N. E. and Wu, Z.: A review on Hilbert-Huang transform: Method and its
applications to geophysical studies, Rev. Geophys., 46, RG2006,
<ext-link xlink:href="http://dx.doi.org/10.1029/2007RG000228" ext-link-type="DOI">10.1029/2007RG000228</ext-link>, 2008.</mixed-citation></ref>
      <ref id="bib1.bib31"><label>31</label><mixed-citation>Janssens-Maenhout, G., Crippa, M., Guizzardi, D., Dentener, F., Muntean, M.,
Pouliot, G., Keating, T., Zhang, Q., Kurokawa, J., Wankmüller, R., Denier
van der Gon, H., Kuenen, J. J. P., Klimont, Z., Frost, G., Darras, S., Koffi,
B., and Li, M.: HTAP_v2.2: a mosaic of regional and global emission grid
maps for 2008 and 2010 to study hemispheric transport of air pollution,
Atmos. Chem. Phys., 15, 11411–11432, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-15-11411-2015" ext-link-type="DOI">10.5194/acp-15-11411-2015</ext-link>, 2015.</mixed-citation></ref>
      <ref id="bib1.bib32"><label>32</label><mixed-citation>Jiang, Z., Worden, J. R., Payne, V. H., Zhu, L., Fischer, E., Walker, T., and
Jones, D. B. A.: Ozone export from East Asia: The role of PAN, J. Geophys.
Res.-Atmos., 121, 6555–6563, <ext-link xlink:href="http://dx.doi.org/10.1002/2016JD024952" ext-link-type="DOI">10.1002/2016JD024952</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib33"><label>33</label><mixed-citation>Kalthoff, N., Bischoff-Gauß, I., Fiebig-Wittmaack, M., Fiedler, F.,
Thürauf, J., Novoa, E., Pizarro, C., Castillo, R., Gallardo, L.,
Rondanelli, R., and Kohler, M.: Mesoscale Wind Regimes in Chile at
30<inline-formula><mml:math id="M177" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>S, J. Appl. Meteorol., 41, 953–970,
<ext-link xlink:href="http://dx.doi.org/10.1175/1520-0450(2002)041&lt;0953:mwrica&gt;2.0.co;2" ext-link-type="DOI">10.1175/1520-0450(2002)041&lt;0953:mwrica&gt;2.0.co;2</ext-link>,
2002.</mixed-citation></ref>
      <ref id="bib1.bib34"><label>34</label><mixed-citation>
Kendall, M. and Stuart, A.: The Advanced Theory of Statistics, Griffin, High
Wycombe, UK, 1983.</mixed-citation></ref>
      <ref id="bib1.bib35"><label>35</label><mixed-citation>Kottek, M., Grieser, J., Beck, C., Rudolf, B., and Rubel, F.: World map of
the Köppen-Geiger climate classification updated, Meteorol. Z., 15,
259–263, <ext-link xlink:href="http://dx.doi.org/10.1127/0941-2948/2006/0130" ext-link-type="DOI">10.1127/0941-2948/2006/0130</ext-link>, 2006.</mixed-citation></ref>
      <ref id="bib1.bib36"><label>36</label><mixed-citation>Lefohn, A. S. and Cooper, O. R.: Introduction to the special issue on
observations and source attribution of ozone in rural regions of the western
United States, Atmos. Environ., 109, 279–281,
<ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2015.03.030" ext-link-type="DOI">10.1016/j.atmosenv.2015.03.030</ext-link>, 2015.</mixed-citation></ref>
      <ref id="bib1.bib37"><label>37</label><mixed-citation>Lin, M., Horowitz, L. W., Oltmans, S. J., Fiore, A. M., and Fan, S.:
Tropospheric ozone trends at Mauna Loa Observatory tied to decadal climate
variability, Nat. Geosci., 7, 136–143, <ext-link xlink:href="http://dx.doi.org/10.1038/ngeo2066" ext-link-type="DOI">10.1038/ngeo2066</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib38"><label>38</label><mixed-citation>Lin, M., Fiore, A. M., Horowitz, L. W., Langford, A. O., Oltmans, S. J.,
Tarasick, D., and Rieder, H. E.: Climate variability modulates western US
ozone air quality in spring via deep stratospheric intrusions, Nature
Communications, 6, 7105, <ext-link xlink:href="http://dx.doi.org/10.1038/ncomms8105" ext-link-type="DOI">10.1038/ncomms8105</ext-link>, 2015.</mixed-citation></ref>
      <ref id="bib1.bib39"><label>39</label><mixed-citation>Monks, P.: A review of the observations and origins of the spring ozone
maximum, Atmos. Environ., 34, 3545–3561,
<ext-link xlink:href="http://dx.doi.org/10.1016/S1352-2310(00)00129-1" ext-link-type="DOI">10.1016/S1352-2310(00)00129-1</ext-link>, 2000.</mixed-citation></ref>
      <ref id="bib1.bib40"><label>40</label><mixed-citation>Muñoz, R. C. and Garreaud, R. D.: Dynamics of the Low-Level Jet off the
West Coast of Subtropical South America, Mon. Weather Rev., 133, 3661–3677,
<ext-link xlink:href="http://dx.doi.org/10.1175/mwr3074.1" ext-link-type="DOI">10.1175/mwr3074.1</ext-link>, 2005.</mixed-citation></ref>
      <ref id="bib1.bib41"><label>41</label><mixed-citation>Myhre, G., Shindell, D., Bréon, F.-M., Collins, W., Fuglestvedt, J.,
Huang, J., Koch, D., Lamarque, J.-F., Lee, D., Mendoza, B., Nakajima, T.,
Robock, A., Stephens, G., Takemura, T., and Zhan, H.: Anthropogenic and
Natural Radiative Forcing, Chapter 8, 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, edited by: Stocker, T. F.,
Qin, D., Plattner, G.-K., Tignor, M. M. B., Allen, S. K., Boschung, J.,
Nauels, A., Xia, Y., Bex, V., and Midgley, P. M., Cambridge University Press,
Cambridge, United Kingdom and New York, NY, USA, 659–740,
<ext-link xlink:href="http://dx.doi.org/10.1017/CBO9781107415324.018" ext-link-type="DOI">10.1017/CBO9781107415324.018</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib42"><label>42</label><mixed-citation>Neu, J. L., Flury, T., Manney, G. L., Santee, M. L., Livesey, N. J., and
Worden, J.: Tropospheric ozone variations governed by changes in
stratospheric circulation, Nat. Geosci., 7, 340–344, <ext-link xlink:href="http://dx.doi.org/10.1038/ngeo2138" ext-link-type="DOI">10.1038/ngeo2138</ext-link>,
2014.</mixed-citation></ref>
      <ref id="bib1.bib43"><label>43</label><mixed-citation>Nguyen, H., Evans, A., Lucas, C., Smith, I., and Timbal, B.: The Hadley
Circulation in Reanalyses: Climatology, Variability, and Change, J. Climate,
26, 3357–3376, <ext-link xlink:href="http://dx.doi.org/10.1175/jcli-d-12-00224.1" ext-link-type="DOI">10.1175/jcli-d-12-00224.1</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib44"><label>44</label><mixed-citation>Nzotungicimpaye, C.-M., Abiodun, B. J., and Steyn, D. G.: Tropospheric ozone
and its regional transport over Cape Town, Atmos. Environ., 87, 228–238,
<ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2014.01.063" ext-link-type="DOI">10.1016/j.atmosenv.2014.01.063</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib45"><label>45</label><mixed-citation>Oltmans, S. J., Lefohn, A. S., Shadwick, D., Harris, J. M., Scheel, H. E.,
Galbally, I., Tarasick, D. W., Johnson, B. J., Brunke, E. G., Claude, H.,
Zeng, G., Nichol, S., Schmidlin, F., Davies, J., Cuevas, E., Redondas, A.,
Naoe, H., Nakano, T., and Kawasato, T.: Recent tropospheric ozone changes –
A pattern dominated by slow or no growth, Atmos. Environ., 67, 331–351,
<ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2012.10.057" ext-link-type="DOI">10.1016/j.atmosenv.2012.10.057</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib46"><label>46</label><mixed-citation>Pante, E. and Simon-Bouhet, B.: marmap: A Package for Importing, Plotting and
Analyzing Bathymetric and Topographic Data in R, PLoS ONE, 8, 6–9,
<ext-link xlink:href="http://dx.doi.org/10.1371/journal.pone.0073051" ext-link-type="DOI">10.1371/journal.pone.0073051</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib47"><label>47</label><mixed-citation>Parrish, D. D., Law, K. S., Staehelin, J., Derwent, R., Cooper, O.`R.,
Tanimoto, H., Volz-Thomas, A., Gilge, S., Scheel, H.-E., Steinbacher, M., and
Chan, E.: Long-term changes in lower tropospheric baseline ozone
concentrations at northern mid-latitudes, Atmos. Chem. Phys., 12,
11485–11504, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-12-11485-2012" ext-link-type="DOI">10.5194/acp-12-11485-2012</ext-link>, 2012.</mixed-citation></ref>
      <ref id="bib1.bib48"><label>48</label><mixed-citation>Parrish, D. D., Law, K. S., Staehelin, J., Derwent, R., Cooper, O. R.,
Tanimoto, H., Volz-Thomas, A., Gilge, S., Scheel, H. E., Steinbacher, M., and
Chan, E.: Lower tropospheric ozone at northern midlatitudes: Changing
seasonal cycle, Geophys. Res. Lett., 40, 1631–1636, <ext-link xlink:href="http://dx.doi.org/10.1002/grl.50303" ext-link-type="DOI">10.1002/grl.50303</ext-link>,
2013.</mixed-citation></ref>
      <ref id="bib1.bib49"><label>49</label><mixed-citation>Rahn, D. A. and Garreaud, R. D.: A synoptic climatology of the near-surface
wind along the west coast of South America, Int. J. Climatol., 34, 780–792,
<ext-link xlink:href="http://dx.doi.org/10.1002/joc.3724" ext-link-type="DOI">10.1002/joc.3724</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib50"><label>50</label><mixed-citation>Reich, P. B. and Amundson, R. G.: Ambient levels of ozone reduce net
photosynthesis in tree and crop species, Science, 230, 566–570,
<ext-link xlink:href="http://dx.doi.org/10.1126/science.230.4725.566" ext-link-type="DOI">10.1126/science.230.4725.566</ext-link>, 1985.</mixed-citation></ref>
      <ref id="bib1.bib51"><label>51</label><mixed-citation>Rondanelli, R., Gallardo, L., and Garreaud, R. D.: Rapid changes in ozone
mixing ratios at Cerro Tololo (30<inline-formula><mml:math id="M178" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>10<inline-formula><mml:math id="M179" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula>S, 70<inline-formula><mml:math id="M180" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>48<inline-formula><mml:math id="M181" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula>W, 2200 m)
in connection with cutoff lows and deep troughs, J. Geophys. Res., 107, 4677,
<ext-link xlink:href="http://dx.doi.org/10.1029/2001JD001334" ext-link-type="DOI">10.1029/2001JD001334</ext-link>, 2002.</mixed-citation></ref>
      <ref id="bib1.bib52"><label>52</label><mixed-citation>Rutllant, J. A., Muõz, R. C., and Garreaud, R. D.: Meteorological
observations on the northern Chilean coast during VOCALS-REx, Atmos. Chem.
Phys., 13, 3409–3422, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-13-3409-2013" ext-link-type="DOI">10.5194/acp-13-3409-2013</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib53"><label>53</label><mixed-citation>Schnell, J. L., Prather, M. J., Josse, B., Naik, V., Horowitz, L. W., Zeng,
G., Shindell, D. T., and Faluvegi, G.: Effect of climate change on surface
ozone over North America, Europe, and East Asia, Geophys. Res. Lett., 43,
3509–3518, <ext-link xlink:href="http://dx.doi.org/10.1002/2016GL068060" ext-link-type="DOI">10.1002/2016GL068060</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib54"><label>54</label><mixed-citation>Sekiya, T. and Sudo, K.: Role of meteorological variability in global
tropospheric ozone during 1970–2008, J. Geophys. Res., 117, D18303,
<ext-link xlink:href="http://dx.doi.org/10.1029/2012JD018054" ext-link-type="DOI">10.1029/2012JD018054</ext-link>, 2012.
</mixed-citation></ref><?xmltex \hack{\newpage}?>
      <ref id="bib1.bib55"><label>55</label><mixed-citation>Shi, Y. and Yamaguchi, Y.: A high-resolution and multi-year emissions
inventory for biomass burning in Southeast Asia during 2001–2010, Atmos.
Environ., 98, 8–16, <ext-link xlink:href="http://dx.doi.org/10.1016/j.atmosenv.2014.08.050" ext-link-type="DOI">10.1016/j.atmosenv.2014.08.050</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib56"><label>56</label><mixed-citation>Sillman, S. and He, D.: Some theoretical results concerning
<inline-formula><mml:math id="M182" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>-<inline-formula><mml:math id="M183" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M184" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>-VOC chemistry and NOx-VOC indicators, J. Geophys.
Res., 107, 4659, <ext-link xlink:href="http://dx.doi.org/10.1029/2001JD001123" ext-link-type="DOI">10.1029/2001JD001123</ext-link>, 2002.</mixed-citation></ref>
      <ref id="bib1.bib57"><label>57</label><mixed-citation>
Simmons, A., Uppala, S., Dee, D., and Kobayashi, S.: ERA-Interim: New ECMWF
reanalysis products from 1989 onwards, ECMWF Newsletter, 110, 25–35, 2007.</mixed-citation></ref>
      <ref id="bib1.bib58"><label>58</label><mixed-citation>Škerlak, B.: Climatology and process studies of tropopause folds,
cross-tropopause exchange, and transport into the boundary layer,
Dissertation, ETH-Zurich, Zürich, Nr. 22036,
<ext-link xlink:href="http://dx.doi.org/10.3929/ethz-a-010256937" ext-link-type="DOI">10.3929/ethz-a-010256937</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib59"><label>59</label><mixed-citation>Škerlak, B., Sprenger, M., and Wernli, H.: A global climatology of
stratosphere-troposphere exchange using the ERA-Interim data set from 1979 to
2011, Atmos. Chem. Phys., 14, 913–937, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-14-913-2014" ext-link-type="DOI">10.5194/acp-14-913-2014</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib60"><label>60</label><mixed-citation>Sofen, E. D., Bowdalo, D., and Evans, M. J.: How to most effectively expand
the global surface ozone observing network, Atmos. Chem. Phys., 16,
1445–1457, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-16-1445-2016" ext-link-type="DOI">10.5194/acp-16-1445-2016</ext-link>, 2016a.</mixed-citation></ref>
      <ref id="bib1.bib61"><label>61</label><mixed-citation>Sofen, E. D., Bowdalo, D., Evans, M. J., Apadula, F., Bonasoni, P., Cupeiro,
M., Ellul, R., Galbally, I. E., Girgzdiene, R., Luppo, S., Mimouni, M.,
Nahas, A. C., Saliba, M., and Tørseth, K.: Gridded global surface ozone
metrics for atmospheric chemistry model evaluation, Earth Syst. Sci. Data, 8,
41–59, <ext-link xlink:href="http://dx.doi.org/10.5194/essd-8-41-2016" ext-link-type="DOI">10.5194/essd-8-41-2016</ext-link>, 2016b.</mixed-citation></ref>
      <ref id="bib1.bib62"><label>62</label><mixed-citation>Sprenger, M. and Wernli, H.: The LAGRANTO Lagrangian analysis tool –
version 2.0, Geosci. Model Dev., 8, 2569–2586,
<ext-link xlink:href="http://dx.doi.org/10.5194/gmd-8-2569-2015" ext-link-type="DOI">10.5194/gmd-8-2569-2015</ext-link>, 2015.</mixed-citation></ref>
      <ref id="bib1.bib63"><label>63</label><mixed-citation>
Staehelin, J., Harris, N. R. P., Appenzeller, C., and Eberhard, J.: Ozone
trends: A review, Rev. Geophys., 39, 231–290, 2001.</mixed-citation></ref>
      <ref id="bib1.bib64"><label>64</label><mixed-citation>Stevenson, D. S., Dentener, F. J., Schultz, M. G., Ellingsen, K., van Noije,
T. P. C., Wild, O., Zeng, G., Amann, M., Atherton, C. S., Bell, N., Bergmann,
D. J., Bey, I., Butler, T., Cofala, J., Collins, W. J., Derwent, R. G.,
Doherty, R. M., Drevet, J., Eskes, H. J., Fiore, A. M., Gauss, M.,
Hauglustaine, D. A., Horowitz, L. W., Isaksen, I. S. A., Krol, M. C.,
Lamarque, J. F., Lawrence, M. G., Montanaro, V., Müller, J. F., Pitari,
G., Prather, M. J., Pyle, J. A., Rast, S., Rodriquez, J. M., Sanderson,
M. G., Savage, N. H., Shindell, D. T., Strahan, S. E., Sudo, K., and Szopa,
S.: Multimodel ensemble simulations of present-day and near-future
tropospheric ozone, J. Geophys. Res., 111, D08301,
<ext-link xlink:href="http://dx.doi.org/10.1029/2005JD006338" ext-link-type="DOI">10.1029/2005JD006338</ext-link>, 2006.</mixed-citation></ref>
      <ref id="bib1.bib65"><label>65</label><mixed-citation>Stohl, A., Wotawa, G., Seibert, P., and Kromp-Kolb, H.: Interpolation Errors
in Wind Fields as a Function of Spatial and Temporal Resolution and Their
Impact on Different Types of Kinematic Trajectories, J. Appl. Meteorol., 34,
2149–2165,
<ext-link xlink:href="http://dx.doi.org/10.1175/1520-0450(1995)034&lt;2149:IEIWFA&gt;2.0.CO;2" ext-link-type="DOI">10.1175/1520-0450(1995)034&lt;2149:IEIWFA&gt;2.0.CO;2</ext-link>,
1995.</mixed-citation></ref>
      <ref id="bib1.bib66"><label>66</label><mixed-citation>Streets, D. G., Yarber, K. F., Woo, J.`H., and Carmichael, G. R.: Biomass
burning in Asia: Annual and seasonal estimates and atmospheric emissions,
Global Biogeochem. Cy., 17, 1099, <ext-link xlink:href="http://dx.doi.org/10.1029/2003GB002040" ext-link-type="DOI">10.1029/2003GB002040</ext-link>, 2003.</mixed-citation></ref>
      <ref id="bib1.bib67"><label>67</label><mixed-citation>Sudo, K. and Akimoto, H.: Global source attribution of tropospheric ozone:
Long-range transport from various source regions, J. Geophys. Res., 112,
D12302, <ext-link xlink:href="http://dx.doi.org/10.1029/2006JD007992" ext-link-type="DOI">10.1029/2006JD007992</ext-link>, 2007.
</mixed-citation></ref><?xmltex \hack{\newpage}?>
      <ref id="bib1.bib68"><label>68</label><mixed-citation>Thompson, A. M.: Southern Hemisphere Additional Ozonesondes (SHADOZ)
1998–2000 tropical ozone climatology 2. Tropospheric variability and the
zonal wave-one, J. Geophys. Res., 108, 8241, <ext-link xlink:href="http://dx.doi.org/10.1029/2002JD002241" ext-link-type="DOI">10.1029/2002JD002241</ext-link>,
2003.</mixed-citation></ref>
      <ref id="bib1.bib69"><label>69</label><mixed-citation>Thompson, A. M., Witte, J. C., Smit, H. G. J., Oltmans, S. J., Johnson,
B. J., Kirchhoff, V. W. J. H., and Schmidlin, F. J.: Southern Hemisphere
Additional Ozonesondes (SHADOZ) 1998-2004 tropical ozone climatology:
3. Instrumentation, station-to-station variability, and evaluation with
simulated flight profiles, J. Geophys. Res., 112, D03304,
<ext-link xlink:href="http://dx.doi.org/10.1029/2005JD007042" ext-link-type="DOI">10.1029/2005JD007042</ext-link>, 2007.</mixed-citation></ref>
      <ref id="bib1.bib70"><label>70</label><mixed-citation>Thompson, A. M., Balashov, N. V., Witte, J. C., Coetzee, J. G. R., Thouret,
V., and Posny, F.: Tropospheric ozone increases over the southern Africa
region: bellwether for rapid growth in Southern Hemisphere pollution?, Atmos.
Chem. Phys., 14, 9855–9869, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-14-9855-2014" ext-link-type="DOI">10.5194/acp-14-9855-2014</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib71"><label>71</label><mixed-citation>Thoning, K. W., Tans, P. P., and Komhyr, W. D.: Atmospheric carbon dioxide at
Mauna Loa Observatory: 2. Analysis of the NOAA GMCC data, 1974–1985,
J. Geophys. Res., 94, 8549–8549, <ext-link xlink:href="http://dx.doi.org/10.1029/JD094iD06p08549" ext-link-type="DOI">10.1029/JD094iD06p08549</ext-link>, 1989.</mixed-citation></ref>
      <ref id="bib1.bib72"><label>72</label><mixed-citation>Verma, S. K., Kawamura, K., Chen, J., Fu, P., and Zhu, C.: Thirteen years of
observations on biomass burning organic tracers over Chichijima Island in the
western North Pacific: An outflow region of Asian aerosols, J. Geophys.
Res.-Atmos., 120, 4155–4168, <ext-link xlink:href="http://dx.doi.org/10.1002/2014JD022224" ext-link-type="DOI">10.1002/2014JD022224</ext-link>, 2015.</mixed-citation></ref>
      <ref id="bib1.bib73"><label>73</label><mixed-citation>Volz, A. and Kley, D.: Evaluation of the Montsouris series of ozone
measurements made in the nineteenth century, Nature, 332, 240–242,
<ext-link xlink:href="http://dx.doi.org/10.1038/332240a0" ext-link-type="DOI">10.1038/332240a0</ext-link>, 1988.
</mixed-citation></ref><?xmltex \hack{\newpage}?>
      <ref id="bib1.bib74"><label>74</label><mixed-citation>Wang, Y., Jacob, D. J., and Logan, J. A.: Global simulation of tropospheric
<inline-formula><mml:math id="M185" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>-<inline-formula><mml:math id="M186" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M187" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>-hydrocarbon chemistry: 3. Origin of tropospheric
ozone and effects of nonmethane hydrocarbons, J. Geophys. Res., 103,
10757–10767, <ext-link xlink:href="http://dx.doi.org/10.1029/98JD00156" ext-link-type="DOI">10.1029/98JD00156</ext-link>, 1998a.</mixed-citation></ref>
      <ref id="bib1.bib75"><label>75</label><mixed-citation>Wang, Y., Logan, J. A., and Jacob, D. J.: Global simulation of tropospheric
<inline-formula><mml:math id="M188" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">O</mml:mi><mml:mn mathvariant="normal">3</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>-<inline-formula><mml:math id="M189" display="inline"><mml:mrow class="chem"><mml:mi mathvariant="normal">NO</mml:mi></mml:mrow></mml:math></inline-formula><inline-formula><mml:math id="M190" display="inline"><mml:msub><mml:mi/><mml:mi>x</mml:mi></mml:msub></mml:math></inline-formula>-hydrocarbon chemistry: 2. Model evaluation and
global ozone budget, J. Geophys. Res., 103, 10727–10755,
<ext-link xlink:href="http://dx.doi.org/10.1029/98JD00157" ext-link-type="DOI">10.1029/98JD00157</ext-link>, 1998b.</mixed-citation></ref>
      <ref id="bib1.bib76"><label>76</label><mixed-citation>Wespes, C., Hurtmans, D., Emmons, L. K., Safieddine, S., Clerbaux, C.,
Edwards, D. P., and Coheur, P.-F.: Ozone variability in the troposphere and
the stratosphere from the first 6 years of IASI observations (2008–2013),
Atmos. Chem. Phys., 16, 5721–5743, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-16-5721-2016" ext-link-type="DOI">10.5194/acp-16-5721-2016</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib77"><label>77</label><mixed-citation>Winer, A. M., Arey, J., Atkinson, R., Aschmann, S. M., Long, W. D., Morrison,
C. L., and Olszyk, D. M.: Emission rates of organics from vegetation in
California's Central Valley, Atmos. Environ. A-Gen., 26, 2647–2659,
<ext-link xlink:href="http://dx.doi.org/10.1016/0960-1686(92)90116-3" ext-link-type="DOI">10.1016/0960-1686(92)90116-3</ext-link>, 1992.</mixed-citation></ref>
      <ref id="bib1.bib78"><label>78</label><mixed-citation>Wu, Z. and Huang, N. E.: Ensemble Empirical Mode Decomposition: A
noise-assisted data analysis method, Advances in Adaptive Data Analysis, 01,
1–41, <ext-link xlink:href="http://dx.doi.org/10.1142/S1793536909000047" ext-link-type="DOI">10.1142/S1793536909000047</ext-link>, 2009.</mixed-citation></ref>
      <ref id="bib1.bib79"><label>79</label><mixed-citation>Ziemke, J. R., Chandra, S., Oman, L. D., and Bhartia, P. K.: A new ENSO index
derived from satellite measurements of column ozone, Atmos. Chem. Phys., 10,
3711–3721, <ext-link xlink:href="http://dx.doi.org/10.5194/acp-10-3711-2010" ext-link-type="DOI">10.5194/acp-10-3711-2010</ext-link>, 2010.</mixed-citation></ref>

  </ref-list><app-group content-type="float"><app><title/>

    </app></app-group></back>
    <!--<article-title-html>Surface ozone in the Southern Hemisphere: 20 years of data from a site with a unique setting in El Tololo, Chile</article-title-html>
<abstract-html><p class="p">The knowledge of surface ozone mole fractions and their global distribution
is of utmost importance due to the impact of ozone on human health and
ecosystems and the central role of ozone in controlling the oxidation
capacity of the troposphere. The availability of long-term ozone records is
far better in the Northern than in the Southern Hemisphere, and recent
analyses of the seven accessible records in the Southern Hemisphere have
shown inconclusive trends. Since late 1995, surface ozone is measured in situ
at <q>El Tololo</q>, a high-altitude (2200 m a.s.l.) and pristine
station in Chile (30° S, 71° W). The dataset has been
recently fully quality controlled and reprocessed. This study presents the
observed ozone trends and annual cycles and identifies key processes driving
these patterns. From 1995 to 2010, an overall positive trend of
 ∼  0.7 ppb decade<sup>−1</sup> is found. Strongest trends per season
are observed in March and April. Highest mole fractions are observed in late
spring (October) and show a strong correlation with ozone transported from
the stratosphere down into the troposphere, as simulated with a model. Over
the 20 years of observations, the springtime ozone maximum has shifted to
earlier times in the year, which, again, is strongly correlated with a
temporal shift in the occurrence of the maximum of simulated stratospheric
ozone transport at the site. We conclude that background ozone at El Tololo
is mainly driven by stratospheric intrusions rather than photochemical
production from anthropogenic and biogenic precursors. The major footprint of
the sampled air masses is located over the Pacific Ocean. Therefore, due to
the negligible influence of local processes, the ozone record also allows
studying the influence of El Niño and La Niña episodes on background
ozone levels in South America. In agreement with previous studies, we find
that, during La Niña conditions, ozone mole fractions reach higher levels
than during El Niño conditions.</p></abstract-html>
<ref-html id="bib1.bib1"><label>1</label><mixed-citation>
Ayers, G. P., Penkett, S. A., Gillet, R. W., Bandy, B., Galbally, I. E.,
Meyer, C. P., Elsworth, C. M., Bentley, S. T., and Forgan, B. W.: Evidence
for photochemical control of ozone concentrations in unpolluted marine air,
Nature, 360, 446–449, <a href="http://dx.doi.org/10.1038/360446a0" target="_blank">doi:10.1038/360446a0</a>, 1992.
</mixed-citation></ref-html>
<ref-html id="bib1.bib2"><label>2</label><mixed-citation>
Barlasina, M. E., Carbajal Benitez, G., Copes, G., Demasi, M., and Cupeiro,
M.: Estudio del ozono troposférico en tres observatorios de la red de
medición del servicio meteorológico nacional – argentina,
Proceedings CONGREMET XI, Mendoza, 29 May–1 June 2012, available at:
<a href="http://www.congremet.prmarg.org/upload/barlasinamaelena.pdf" target="_blank">http://www.congremet.prmarg.org/upload/barlasinamaelena.pdf</a> (last
access: 20 May 2017), 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib3"><label>3</label><mixed-citation>
Barnhart, B. L., Nandage, H. K. W., and Eichinger, W.: Assessing
Discontinuous Data Using Ensemble Empirical Mode Decomposition, Advances in
Adaptive Data Analysis, 03, 483–491, <a href="http://dx.doi.org/10.1142/s179353691100091x" target="_blank">doi:10.1142/s179353691100091x</a>, 2011.
</mixed-citation></ref-html>
<ref-html id="bib1.bib4"><label>4</label><mixed-citation>
Baylon, P., Jaffe, D. A., Wigder, N. L., Gao, H., and Hee, J.: Ozone
enhancement in western US wildfire plumes at the Mt. Bachelor Observatory:
The role of NO<sub><i>x</i></sub>, Atmos. Environ., 109, 297–304,
<a href="http://dx.doi.org/10.1016/j.atmosenv.2014.09.013" target="_blank">doi:10.1016/j.atmosenv.2014.09.013</a>, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib5"><label>5</label><mixed-citation>
Bloomer, B. J., Vinnikov, K. Y., and Dickerson, R. R.: Changes in seasonal
and diurnal cycles of ozone and temperature in the eastern U.S, Atmos.
Environ., 44, 2543–2551, <a href="http://dx.doi.org/10.1016/j.atmosenv.2010.04.031" target="_blank">doi:10.1016/j.atmosenv.2010.04.031</a>, 2010.
</mixed-citation></ref-html>
<ref-html id="bib1.bib6"><label>6</label><mixed-citation>
Brook, R. D.: Inhalation of Fine Particulate Air Pollution and Ozone Causes
Acute Arterial Vasoconstriction in Healthy Adults, Circulation, 105,
1534–1536, <a href="http://dx.doi.org/10.1161/01.CIR.0000013838.94747.64" target="_blank">doi:10.1161/01.CIR.0000013838.94747.64</a>, 2002.
</mixed-citation></ref-html>
<ref-html id="bib1.bib7"><label>7</label><mixed-citation>
Carslaw, D. C.: On the changing seasonal cycles and trends of ozone at Mace
Head, Ireland, Atmos. Chem. Phys., 5, 3441–3450,
<a href="http://dx.doi.org/10.5194/acp-5-3441-2005" target="_blank">doi:10.5194/acp-5-3441-2005</a>, 2005.
</mixed-citation></ref-html>
<ref-html id="bib1.bib8"><label>8</label><mixed-citation>
Choi, J., Son, S.-W., Lu, J., and Min, S.-K.: Further observational evidence
of Hadley cell widening in the Southern Hemisphere, Geophys. Res. Lett., 41,
2590–2597, <a href="http://dx.doi.org/10.1002/2014GL059426" target="_blank">doi:10.1002/2014GL059426</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib9"><label>9</label><mixed-citation>
Collins, W. J., Derwent, R. G., Garnier, B., Johnson, C. E., Sanderson,
M. G., and Stevenson, D. S.: Effect of stratosphere-troposphere exchange on
the future tropospheric ozone trend, J. Geophys. Res., 108, 8528,
10.1029/2002JD002617, 2003.
</mixed-citation></ref-html>
<ref-html id="bib1.bib10"><label>10</label><mixed-citation>
Combrink, J., Diab, R. D., Sokolic, F., and Brunke, E. G.: Relationship
between surface, free tropospheric and total column ozone in two contrasting
areas in South Africa, Atmos. Environ., 29, 685–691,
<a href="http://dx.doi.org/10.1016/1352-2310(94)00313-A" target="_blank">doi:10.1016/1352-2310(94)00313-A</a>, 1995.
</mixed-citation></ref-html>
<ref-html id="bib1.bib11"><label>11</label><mixed-citation>
Cooper, O. R., Gao, R. S., Tarasick, D., Leblanc, T., and Sweeney, C.:
Long-term ozone trends at rural ozone monitoring sites across the United
States, 1990–2010, J. Geophys. Res., 117, 1990–2010,
<a href="http://dx.doi.org/10.1029/2012JD018261" target="_blank">doi:10.1029/2012JD018261</a>, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib12"><label>12</label><mixed-citation>
Cooper, O. R., Parrish, D. D., Ziemke, J., Balashov, N. V., Cupeiro, M.,
Galbally, I. E., Gilge, S., Horowitz, L., Jensen, N. R., Lamarque, J. F.,
Naik, V., Oltmans, S. J., Schwab, J., Shindell, D. T., Thompson, A. M.,
Thouret, V., Wang, Y., and Zbinden, R. M.: Global distribution and trends of
tropospheric ozone: An observation-based review, Elementa, 2, 000029,
<a href="http://dx.doi.org/10.12952/journal.elementa.000029" target="_blank">doi:10.12952/journal.elementa.000029</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib13"><label>13</label><mixed-citation>
Crutzen, P.: A discussion of the chemistry of some minor constituents in the
stratosphere and troposphere, Pure Appl. Geophys., 106, 1385–1399,
<a href="http://dx.doi.org/10.1007/bf00881092" target="_blank">doi:10.1007/bf00881092</a>, 1973.

</mixed-citation></ref-html>
<ref-html id="bib1.bib14"><label>14</label><mixed-citation>
Crutzen, P. J.: Ozone production rates in an oxygen-hydrogen-nitrogen oxide
atmosphere, J. Geophys. Res., 76, 7311–7311, <a href="http://dx.doi.org/10.1029/JC076i030p07311" target="_blank">doi:10.1029/JC076i030p07311</a>,
1971.
</mixed-citation></ref-html>
<ref-html id="bib1.bib15"><label>15</label><mixed-citation>
Crutzen, P. J. and Zimmermann, P. H.: The changing photochemistry of the
troposphere, Tellus B, 43, 136–151,
<a href="http://dx.doi.org/10.1034/j.1600-0889.1991.t01-1-00012.x" target="_blank">doi:10.1034/j.1600-0889.1991.t01-1-00012.x</a>, 1991.
</mixed-citation></ref-html>
<ref-html id="bib1.bib16"><label>16</label><mixed-citation>
Derwent, R. G., Jenkin, M. E., Saunders, S. M., and Pilling, M. J.:
Photochemical ozone creation potentials for organic compounds in northwest
Europe calculated with a master chemical mechanism, Atmos. Environ., 32,
2429–2441, <a href="http://dx.doi.org/10.1016/S1352-2310(98)00053-3" target="_blank">doi:10.1016/S1352-2310(98)00053-3</a>, 1998.
</mixed-citation></ref-html>
<ref-html id="bib1.bib17"><label>17</label><mixed-citation>
Derwent, R. G., Simmonds, P. G., Manning, A. J., and Spain, T. G.: Trends
over a 20-year period from 1987 to 2007 in surface ozone at the atmospheric
research station, Mace Head, Ireland, Atmos. Environ., 41, 9091–9098,
<a href="http://dx.doi.org/10.1016/j.atmosenv.2007.08.008" target="_blank">doi:10.1016/j.atmosenv.2007.08.008</a>, 2007.
</mixed-citation></ref-html>
<ref-html id="bib1.bib18"><label>18</label><mixed-citation>
Derwent, R. G., Manning, A. J., Simmonds, P. G., Spain, T. G., and O'Doherty,
S.: Analysis and interpretation of 25 years of ozone observations at the Mace
Head Atmospheric Research Station on the Atlantic Ocean coast of Ireland from
1987 to 2012, Atmos. Environ., 80, 361–368,
<a href="http://dx.doi.org/10.1016/j.atmosenv.2013.08.003" target="_blank">doi:10.1016/j.atmosenv.2013.08.003</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib19"><label>19</label><mixed-citation>
Doherty, R. M., Stevenson, D. S., Johnson, C. E., Collins, W. J., and
Sanderson, M. G.: Tropospheric ozone and El Niño–Southern Oscillation:
Influence of atmospheric dynamics, biomass burning emissions, and future
climate change, J. Geophys. Res., 111, D19304, <a href="http://dx.doi.org/10.1029/2005JD006849" target="_blank">doi:10.1029/2005JD006849</a>,
2006.
</mixed-citation></ref-html>
<ref-html id="bib1.bib20"><label>20</label><mixed-citation>
Elshorbany, Y. F., Kleffmann, J., Kurtenbach, R., Rubio, M., Lissi, E.,
Villena, G., Gramsch, E., Rickard, A. R., Pilling, M. J., and Wiesen, P.:
Summertime photochemical ozone formation in Santiago, Chile, Atmos. Environ.,
43, 6398–6407, <a href="http://dx.doi.org/10.1016/j.atmosenv.2009.08.047" target="_blank">doi:10.1016/j.atmosenv.2009.08.047</a>, 2009.
</mixed-citation></ref-html>
<ref-html id="bib1.bib21"><label>21</label><mixed-citation>
Fiscus, E. L., Booker, F. L., and Burkey, K. O.: Crop responses to ozone:
Uptake, modes of action, carbon assimilation and partitioning, Plant Cell
Environ., 28, 997–1011, <a href="http://dx.doi.org/10.1111/j.1365-3040.2005.01349.x" target="_blank">doi:10.1111/j.1365-3040.2005.01349.x</a>, 2005.
</mixed-citation></ref-html>
<ref-html id="bib1.bib22"><label>22</label><mixed-citation>
Fuenzalida, H. A., Sánchez, R., and Garreaud, R. D.: A climatology of
cutoff lows in the Southern Hemisphere, J. Geophys. Res., 110, D18101,
<a href="http://dx.doi.org/10.1029/2005JD005934" target="_blank">doi:10.1029/2005JD005934</a>, 2005.
</mixed-citation></ref-html>
<ref-html id="bib1.bib23"><label>23</label><mixed-citation>
Galbally, I.: Some Measurements of Ozone Variation and Destruction in the
Atmospheric Surface Layer, Nature, 218, 456–457, <a href="http://dx.doi.org/10.1038/218456a0" target="_blank">doi:10.1038/218456a0</a>,
1968.
</mixed-citation></ref-html>
<ref-html id="bib1.bib24"><label>24</label><mixed-citation>
Gallardo, L., Carrasco, J., and Olivares, G.: An analysis of ozone
measurements at Cerro Tololo (30°S, 70°W, 2200 m.a.s.l.) in
Chile, Tellus B, 52, 50–59, <a href="http://dx.doi.org/10.1034/j.1600-0889.2000.00959.x" target="_blank">doi:10.1034/j.1600-0889.2000.00959.x</a>, 2000.
</mixed-citation></ref-html>
<ref-html id="bib1.bib25"><label>25</label><mixed-citation>
Garreaud, R. D. and Muñoz, R. C.: The Low-Level Jet off the West Coast of
Subtropical South America: Structure and Variability, Mon. Weather Rev., 133,
2246–2261, <a href="http://dx.doi.org/10.1175/mwr2972.1" target="_blank">doi:10.1175/mwr2972.1</a>, 2005.
</mixed-citation></ref-html>
<ref-html id="bib1.bib26"><label>26</label><mixed-citation>
GAW: GAW Report No. 209: Guidelines for Continuous Measurements of Ozone in
the Troposphere, WMO and GAW, WMO-No. 1110, 82 pp., 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib27"><label>27</label><mixed-citation>
Geiger, R.: Überarbeitete Neuausgabe von Geiger, R:
Köppen-Geiger/Klima der Erde, Wandkarte 1 : 16 Mill., Klett-Perthes,
Gotha, 1961.
</mixed-citation></ref-html>
<ref-html id="bib1.bib28"><label>28</label><mixed-citation>
Hegglin, M. I. and Shepherd, T. G.: Large climate-induced changes in
ultraviolet index and stratosphere-to-troposphere ozone flux, Nat. Geosci.,
2, 687–691, <a href="http://dx.doi.org/10.1038/ngeo604" target="_blank">doi:10.1038/ngeo604</a>, 2009.
</mixed-citation></ref-html>
<ref-html id="bib1.bib29"><label>29</label><mixed-citation>
Holton, J. R., Haynes, P. H., McIntyre, M. E., Douglass, A. R., Rood, R. B.,
and Pfister, L.: Stratosphere–troposphere exchange, Rev. Geophys., 33,
403–403, <a href="http://dx.doi.org/10.1029/95RG02097" target="_blank">doi:10.1029/95RG02097</a>, 1995.
</mixed-citation></ref-html>
<ref-html id="bib1.bib30"><label>30</label><mixed-citation>
Huang, N. E. and Wu, Z.: A review on Hilbert-Huang transform: Method and its
applications to geophysical studies, Rev. Geophys., 46, RG2006,
<a href="http://dx.doi.org/10.1029/2007RG000228" target="_blank">doi:10.1029/2007RG000228</a>, 2008.
</mixed-citation></ref-html>
<ref-html id="bib1.bib31"><label>31</label><mixed-citation>
Janssens-Maenhout, G., Crippa, M., Guizzardi, D., Dentener, F., Muntean, M.,
Pouliot, G., Keating, T., Zhang, Q., Kurokawa, J., Wankmüller, R., Denier
van der Gon, H., Kuenen, J. J. P., Klimont, Z., Frost, G., Darras, S., Koffi,
B., and Li, M.: HTAP_v2.2: a mosaic of regional and global emission grid
maps for 2008 and 2010 to study hemispheric transport of air pollution,
Atmos. Chem. Phys., 15, 11411–11432, <a href="http://dx.doi.org/10.5194/acp-15-11411-2015" target="_blank">doi:10.5194/acp-15-11411-2015</a>, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib32"><label>32</label><mixed-citation>
Jiang, Z., Worden, J. R., Payne, V. H., Zhu, L., Fischer, E., Walker, T., and
Jones, D. B. A.: Ozone export from East Asia: The role of PAN, J. Geophys.
Res.-Atmos., 121, 6555–6563, <a href="http://dx.doi.org/10.1002/2016JD024952" target="_blank">doi:10.1002/2016JD024952</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib33"><label>33</label><mixed-citation>
Kalthoff, N., Bischoff-Gauß, I., Fiebig-Wittmaack, M., Fiedler, F.,
Thürauf, J., Novoa, E., Pizarro, C., Castillo, R., Gallardo, L.,
Rondanelli, R., and Kohler, M.: Mesoscale Wind Regimes in Chile at
30°S, J. Appl. Meteorol., 41, 953–970,
<a href="http://dx.doi.org/10.1175/1520-0450(2002)041&lt;0953:mwrica&gt;2.0.co;2" target="_blank">doi:10.1175/1520-0450(2002)041&lt;0953:mwrica&gt;2.0.co;2</a>,
2002.
</mixed-citation></ref-html>
<ref-html id="bib1.bib34"><label>34</label><mixed-citation>
Kendall, M. and Stuart, A.: The Advanced Theory of Statistics, Griffin, High
Wycombe, UK, 1983.
</mixed-citation></ref-html>
<ref-html id="bib1.bib35"><label>35</label><mixed-citation>
Kottek, M., Grieser, J., Beck, C., Rudolf, B., and Rubel, F.: World map of
the Köppen-Geiger climate classification updated, Meteorol. Z., 15,
259–263, <a href="http://dx.doi.org/10.1127/0941-2948/2006/0130" target="_blank">doi:10.1127/0941-2948/2006/0130</a>, 2006.
</mixed-citation></ref-html>
<ref-html id="bib1.bib36"><label>36</label><mixed-citation>
Lefohn, A. S. and Cooper, O. R.: Introduction to the special issue on
observations and source attribution of ozone in rural regions of the western
United States, Atmos. Environ., 109, 279–281,
<a href="http://dx.doi.org/10.1016/j.atmosenv.2015.03.030" target="_blank">doi:10.1016/j.atmosenv.2015.03.030</a>, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib37"><label>37</label><mixed-citation>
Lin, M., Horowitz, L. W., Oltmans, S. J., Fiore, A. M., and Fan, S.:
Tropospheric ozone trends at Mauna Loa Observatory tied to decadal climate
variability, Nat. Geosci., 7, 136–143, <a href="http://dx.doi.org/10.1038/ngeo2066" target="_blank">doi:10.1038/ngeo2066</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib38"><label>38</label><mixed-citation>
Lin, M., Fiore, A. M., Horowitz, L. W., Langford, A. O., Oltmans, S. J.,
Tarasick, D., and Rieder, H. E.: Climate variability modulates western US
ozone air quality in spring via deep stratospheric intrusions, Nature
Communications, 6, 7105, <a href="http://dx.doi.org/10.1038/ncomms8105" target="_blank">doi:10.1038/ncomms8105</a>, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib39"><label>39</label><mixed-citation>
Monks, P.: A review of the observations and origins of the spring ozone
maximum, Atmos. Environ., 34, 3545–3561,
<a href="http://dx.doi.org/10.1016/S1352-2310(00)00129-1" target="_blank">doi:10.1016/S1352-2310(00)00129-1</a>, 2000.
</mixed-citation></ref-html>
<ref-html id="bib1.bib40"><label>40</label><mixed-citation>
Muñoz, R. C. and Garreaud, R. D.: Dynamics of the Low-Level Jet off the
West Coast of Subtropical South America, Mon. Weather Rev., 133, 3661–3677,
<a href="http://dx.doi.org/10.1175/mwr3074.1" target="_blank">doi:10.1175/mwr3074.1</a>, 2005.
</mixed-citation></ref-html>
<ref-html id="bib1.bib41"><label>41</label><mixed-citation>
Myhre, G., Shindell, D., Bréon, F.-M., Collins, W., Fuglestvedt, J.,
Huang, J., Koch, D., Lamarque, J.-F., Lee, D., Mendoza, B., Nakajima, T.,
Robock, A., Stephens, G., Takemura, T., and Zhan, H.: Anthropogenic and
Natural Radiative Forcing, Chapter 8, 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, edited by: Stocker, T. F.,
Qin, D., Plattner, G.-K., Tignor, M. M. B., Allen, S. K., Boschung, J.,
Nauels, A., Xia, Y., Bex, V., and Midgley, P. M., Cambridge University Press,
Cambridge, United Kingdom and New York, NY, USA, 659–740,
<a href="http://dx.doi.org/10.1017/CBO9781107415324.018" target="_blank">doi:10.1017/CBO9781107415324.018</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib42"><label>42</label><mixed-citation>
Neu, J. L., Flury, T., Manney, G. L., Santee, M. L., Livesey, N. J., and
Worden, J.: Tropospheric ozone variations governed by changes in
stratospheric circulation, Nat. Geosci., 7, 340–344, <a href="http://dx.doi.org/10.1038/ngeo2138" target="_blank">doi:10.1038/ngeo2138</a>,
2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib43"><label>43</label><mixed-citation>
Nguyen, H., Evans, A., Lucas, C., Smith, I., and Timbal, B.: The Hadley
Circulation in Reanalyses: Climatology, Variability, and Change, J. Climate,
26, 3357–3376, <a href="http://dx.doi.org/10.1175/jcli-d-12-00224.1" target="_blank">doi:10.1175/jcli-d-12-00224.1</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib44"><label>44</label><mixed-citation>
Nzotungicimpaye, C.-M., Abiodun, B. J., and Steyn, D. G.: Tropospheric ozone
and its regional transport over Cape Town, Atmos. Environ., 87, 228–238,
<a href="http://dx.doi.org/10.1016/j.atmosenv.2014.01.063" target="_blank">doi:10.1016/j.atmosenv.2014.01.063</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib45"><label>45</label><mixed-citation>
Oltmans, S. J., Lefohn, A. S., Shadwick, D., Harris, J. M., Scheel, H. E.,
Galbally, I., Tarasick, D. W., Johnson, B. J., Brunke, E. G., Claude, H.,
Zeng, G., Nichol, S., Schmidlin, F., Davies, J., Cuevas, E., Redondas, A.,
Naoe, H., Nakano, T., and Kawasato, T.: Recent tropospheric ozone changes –
A pattern dominated by slow or no growth, Atmos. Environ., 67, 331–351,
<a href="http://dx.doi.org/10.1016/j.atmosenv.2012.10.057" target="_blank">doi:10.1016/j.atmosenv.2012.10.057</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib46"><label>46</label><mixed-citation>
Pante, E. and Simon-Bouhet, B.: marmap: A Package for Importing, Plotting and
Analyzing Bathymetric and Topographic Data in R, PLoS ONE, 8, 6–9,
<a href="http://dx.doi.org/10.1371/journal.pone.0073051" target="_blank">doi:10.1371/journal.pone.0073051</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib47"><label>47</label><mixed-citation>
Parrish, D. D., Law, K. S., Staehelin, J., Derwent, R., Cooper, O.`R.,
Tanimoto, H., Volz-Thomas, A., Gilge, S., Scheel, H.-E., Steinbacher, M., and
Chan, E.: Long-term changes in lower tropospheric baseline ozone
concentrations at northern mid-latitudes, Atmos. Chem. Phys., 12,
11485–11504, <a href="http://dx.doi.org/10.5194/acp-12-11485-2012" target="_blank">doi:10.5194/acp-12-11485-2012</a>, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib48"><label>48</label><mixed-citation>
Parrish, D. D., Law, K. S., Staehelin, J., Derwent, R., Cooper, O. R.,
Tanimoto, H., Volz-Thomas, A., Gilge, S., Scheel, H. E., Steinbacher, M., and
Chan, E.: Lower tropospheric ozone at northern midlatitudes: Changing
seasonal cycle, Geophys. Res. Lett., 40, 1631–1636, <a href="http://dx.doi.org/10.1002/grl.50303" target="_blank">doi:10.1002/grl.50303</a>,
2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib49"><label>49</label><mixed-citation>
Rahn, D. A. and Garreaud, R. D.: A synoptic climatology of the near-surface
wind along the west coast of South America, Int. J. Climatol., 34, 780–792,
<a href="http://dx.doi.org/10.1002/joc.3724" target="_blank">doi:10.1002/joc.3724</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib50"><label>50</label><mixed-citation>
Reich, P. B. and Amundson, R. G.: Ambient levels of ozone reduce net
photosynthesis in tree and crop species, Science, 230, 566–570,
<a href="http://dx.doi.org/10.1126/science.230.4725.566" target="_blank">doi:10.1126/science.230.4725.566</a>, 1985.
</mixed-citation></ref-html>
<ref-html id="bib1.bib51"><label>51</label><mixed-citation>
Rondanelli, R., Gallardo, L., and Garreaud, R. D.: Rapid changes in ozone
mixing ratios at Cerro Tololo (30°10′S, 70°48′W, 2200 m)
in connection with cutoff lows and deep troughs, J. Geophys. Res., 107, 4677,
<a href="http://dx.doi.org/10.1029/2001JD001334" target="_blank">doi:10.1029/2001JD001334</a>, 2002.
</mixed-citation></ref-html>
<ref-html id="bib1.bib52"><label>52</label><mixed-citation>
Rutllant, J. A., Muõz, R. C., and Garreaud, R. D.: Meteorological
observations on the northern Chilean coast during VOCALS-REx, Atmos. Chem.
Phys., 13, 3409–3422, <a href="http://dx.doi.org/10.5194/acp-13-3409-2013" target="_blank">doi:10.5194/acp-13-3409-2013</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib53"><label>53</label><mixed-citation>
Schnell, J. L., Prather, M. J., Josse, B., Naik, V., Horowitz, L. W., Zeng,
G., Shindell, D. T., and Faluvegi, G.: Effect of climate change on surface
ozone over North America, Europe, and East Asia, Geophys. Res. Lett., 43,
3509–3518, <a href="http://dx.doi.org/10.1002/2016GL068060" target="_blank">doi:10.1002/2016GL068060</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib54"><label>54</label><mixed-citation>
Sekiya, T. and Sudo, K.: Role of meteorological variability in global
tropospheric ozone during 1970–2008, J. Geophys. Res., 117, D18303,
<a href="http://dx.doi.org/10.1029/2012JD018054" target="_blank">doi:10.1029/2012JD018054</a>, 2012.

</mixed-citation></ref-html>
<ref-html id="bib1.bib55"><label>55</label><mixed-citation>
Shi, Y. and Yamaguchi, Y.: A high-resolution and multi-year emissions
inventory for biomass burning in Southeast Asia during 2001–2010, Atmos.
Environ., 98, 8–16, <a href="http://dx.doi.org/10.1016/j.atmosenv.2014.08.050" target="_blank">doi:10.1016/j.atmosenv.2014.08.050</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib56"><label>56</label><mixed-citation>
Sillman, S. and He, D.: Some theoretical results concerning
O<sub>3</sub>-NO<sub><i>x</i></sub>-VOC chemistry and NOx-VOC indicators, J. Geophys.
Res., 107, 4659, <a href="http://dx.doi.org/10.1029/2001JD001123" target="_blank">doi:10.1029/2001JD001123</a>, 2002.
</mixed-citation></ref-html>
<ref-html id="bib1.bib57"><label>57</label><mixed-citation>
Simmons, A., Uppala, S., Dee, D., and Kobayashi, S.: ERA-Interim: New ECMWF
reanalysis products from 1989 onwards, ECMWF Newsletter, 110, 25–35, 2007.
</mixed-citation></ref-html>
<ref-html id="bib1.bib58"><label>58</label><mixed-citation>
Škerlak, B.: Climatology and process studies of tropopause folds,
cross-tropopause exchange, and transport into the boundary layer,
Dissertation, ETH-Zurich, Zürich, Nr. 22036,
<a href="http://dx.doi.org/10.3929/ethz-a-010256937" target="_blank">doi:10.3929/ethz-a-010256937</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib59"><label>59</label><mixed-citation>
Škerlak, B., Sprenger, M., and Wernli, H.: A global climatology of
stratosphere-troposphere exchange using the ERA-Interim data set from 1979 to
2011, Atmos. Chem. Phys., 14, 913–937, <a href="http://dx.doi.org/10.5194/acp-14-913-2014" target="_blank">doi:10.5194/acp-14-913-2014</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib60"><label>60</label><mixed-citation>
Sofen, E. D., Bowdalo, D., and Evans, M. J.: How to most effectively expand
the global surface ozone observing network, Atmos. Chem. Phys., 16,
1445–1457, <a href="http://dx.doi.org/10.5194/acp-16-1445-2016" target="_blank">doi:10.5194/acp-16-1445-2016</a>, 2016a.
</mixed-citation></ref-html>
<ref-html id="bib1.bib61"><label>61</label><mixed-citation>
Sofen, E. D., Bowdalo, D., Evans, M. J., Apadula, F., Bonasoni, P., Cupeiro,
M., Ellul, R., Galbally, I. E., Girgzdiene, R., Luppo, S., Mimouni, M.,
Nahas, A. C., Saliba, M., and Tørseth, K.: Gridded global surface ozone
metrics for atmospheric chemistry model evaluation, Earth Syst. Sci. Data, 8,
41–59, <a href="http://dx.doi.org/10.5194/essd-8-41-2016" target="_blank">doi:10.5194/essd-8-41-2016</a>, 2016b.
</mixed-citation></ref-html>
<ref-html id="bib1.bib62"><label>62</label><mixed-citation>
Sprenger, M. and Wernli, H.: The LAGRANTO Lagrangian analysis tool –
version 2.0, Geosci. Model Dev., 8, 2569–2586,
<a href="http://dx.doi.org/10.5194/gmd-8-2569-2015" target="_blank">doi:10.5194/gmd-8-2569-2015</a>, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib63"><label>63</label><mixed-citation>
Staehelin, J., Harris, N. R. P., Appenzeller, C., and Eberhard, J.: Ozone
trends: A review, Rev. Geophys., 39, 231–290, 2001.
</mixed-citation></ref-html>
<ref-html id="bib1.bib64"><label>64</label><mixed-citation>
Stevenson, D. S., Dentener, F. J., Schultz, M. G., Ellingsen, K., van Noije,
T. P. C., Wild, O., Zeng, G., Amann, M., Atherton, C. S., Bell, N., Bergmann,
D. J., Bey, I., Butler, T., Cofala, J., Collins, W. J., Derwent, R. G.,
Doherty, R. M., Drevet, J., Eskes, H. J., Fiore, A. M., Gauss, M.,
Hauglustaine, D. A., Horowitz, L. W., Isaksen, I. S. A., Krol, M. C.,
Lamarque, J. F., Lawrence, M. G., Montanaro, V., Müller, J. F., Pitari,
G., Prather, M. J., Pyle, J. A., Rast, S., Rodriquez, J. M., Sanderson,
M. G., Savage, N. H., Shindell, D. T., Strahan, S. E., Sudo, K., and Szopa,
S.: Multimodel ensemble simulations of present-day and near-future
tropospheric ozone, J. Geophys. Res., 111, D08301,
<a href="http://dx.doi.org/10.1029/2005JD006338" target="_blank">doi:10.1029/2005JD006338</a>, 2006.
</mixed-citation></ref-html>
<ref-html id="bib1.bib65"><label>65</label><mixed-citation>
Stohl, A., Wotawa, G., Seibert, P., and Kromp-Kolb, H.: Interpolation Errors
in Wind Fields as a Function of Spatial and Temporal Resolution and Their
Impact on Different Types of Kinematic Trajectories, J. Appl. Meteorol., 34,
2149–2165,
<a href="http://dx.doi.org/10.1175/1520-0450(1995)034&lt;2149:IEIWFA&gt;2.0.CO;2" target="_blank">doi:10.1175/1520-0450(1995)034&lt;2149:IEIWFA&gt;2.0.CO;2</a>,
1995.
</mixed-citation></ref-html>
<ref-html id="bib1.bib66"><label>66</label><mixed-citation>
Streets, D. G., Yarber, K. F., Woo, J.`H., and Carmichael, G. R.: Biomass
burning in Asia: Annual and seasonal estimates and atmospheric emissions,
Global Biogeochem. Cy., 17, 1099, <a href="http://dx.doi.org/10.1029/2003GB002040" target="_blank">doi:10.1029/2003GB002040</a>, 2003.
</mixed-citation></ref-html>
<ref-html id="bib1.bib67"><label>67</label><mixed-citation>
Sudo, K. and Akimoto, H.: Global source attribution of tropospheric ozone:
Long-range transport from various source regions, J. Geophys. Res., 112,
D12302, <a href="http://dx.doi.org/10.1029/2006JD007992" target="_blank">doi:10.1029/2006JD007992</a>, 2007.

</mixed-citation></ref-html>
<ref-html id="bib1.bib68"><label>68</label><mixed-citation>
Thompson, A. M.: Southern Hemisphere Additional Ozonesondes (SHADOZ)
1998–2000 tropical ozone climatology 2. Tropospheric variability and the
zonal wave-one, J. Geophys. Res., 108, 8241, <a href="http://dx.doi.org/10.1029/2002JD002241" target="_blank">doi:10.1029/2002JD002241</a>,
2003.
</mixed-citation></ref-html>
<ref-html id="bib1.bib69"><label>69</label><mixed-citation>
Thompson, A. M., Witte, J. C., Smit, H. G. J., Oltmans, S. J., Johnson,
B. J., Kirchhoff, V. W. J. H., and Schmidlin, F. J.: Southern Hemisphere
Additional Ozonesondes (SHADOZ) 1998-2004 tropical ozone climatology:
3. Instrumentation, station-to-station variability, and evaluation with
simulated flight profiles, J. Geophys. Res., 112, D03304,
<a href="http://dx.doi.org/10.1029/2005JD007042" target="_blank">doi:10.1029/2005JD007042</a>, 2007.
</mixed-citation></ref-html>
<ref-html id="bib1.bib70"><label>70</label><mixed-citation>
Thompson, A. M., Balashov, N. V., Witte, J. C., Coetzee, J. G. R., Thouret,
V., and Posny, F.: Tropospheric ozone increases over the southern Africa
region: bellwether for rapid growth in Southern Hemisphere pollution?, Atmos.
Chem. Phys., 14, 9855–9869, <a href="http://dx.doi.org/10.5194/acp-14-9855-2014" target="_blank">doi:10.5194/acp-14-9855-2014</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib71"><label>71</label><mixed-citation>
Thoning, K. W., Tans, P. P., and Komhyr, W. D.: Atmospheric carbon dioxide at
Mauna Loa Observatory: 2. Analysis of the NOAA GMCC data, 1974–1985,
J. Geophys. Res., 94, 8549–8549, <a href="http://dx.doi.org/10.1029/JD094iD06p08549" target="_blank">doi:10.1029/JD094iD06p08549</a>, 1989.
</mixed-citation></ref-html>
<ref-html id="bib1.bib72"><label>72</label><mixed-citation>
Verma, S. K., Kawamura, K., Chen, J., Fu, P., and Zhu, C.: Thirteen years of
observations on biomass burning organic tracers over Chichijima Island in the
western North Pacific: An outflow region of Asian aerosols, J. Geophys.
Res.-Atmos., 120, 4155–4168, <a href="http://dx.doi.org/10.1002/2014JD022224" target="_blank">doi:10.1002/2014JD022224</a>, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib73"><label>73</label><mixed-citation>
Volz, A. and Kley, D.: Evaluation of the Montsouris series of ozone
measurements made in the nineteenth century, Nature, 332, 240–242,
<a href="http://dx.doi.org/10.1038/332240a0" target="_blank">doi:10.1038/332240a0</a>, 1988.

</mixed-citation></ref-html>
<ref-html id="bib1.bib74"><label>74</label><mixed-citation>
Wang, Y., Jacob, D. J., and Logan, J. A.: Global simulation of tropospheric
O<sub>3</sub>-NO<sub><i>x</i></sub>-hydrocarbon chemistry: 3. Origin of tropospheric
ozone and effects of nonmethane hydrocarbons, J. Geophys. Res., 103,
10757–10767, <a href="http://dx.doi.org/10.1029/98JD00156" target="_blank">doi:10.1029/98JD00156</a>, 1998a.
</mixed-citation></ref-html>
<ref-html id="bib1.bib75"><label>75</label><mixed-citation>
Wang, Y., Logan, J. A., and Jacob, D. J.: Global simulation of tropospheric
O<sub>3</sub>-NO<sub><i>x</i></sub>-hydrocarbon chemistry: 2. Model evaluation and
global ozone budget, J. Geophys. Res., 103, 10727–10755,
<a href="http://dx.doi.org/10.1029/98JD00157" target="_blank">doi:10.1029/98JD00157</a>, 1998b.
</mixed-citation></ref-html>
<ref-html id="bib1.bib76"><label>76</label><mixed-citation>
Wespes, C., Hurtmans, D., Emmons, L. K., Safieddine, S., Clerbaux, C.,
Edwards, D. P., and Coheur, P.-F.: Ozone variability in the troposphere and
the stratosphere from the first 6 years of IASI observations (2008–2013),
Atmos. Chem. Phys., 16, 5721–5743, <a href="http://dx.doi.org/10.5194/acp-16-5721-2016" target="_blank">doi:10.5194/acp-16-5721-2016</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib77"><label>77</label><mixed-citation>
Winer, A. M., Arey, J., Atkinson, R., Aschmann, S. M., Long, W. D., Morrison,
C. L., and Olszyk, D. M.: Emission rates of organics from vegetation in
California's Central Valley, Atmos. Environ. A-Gen., 26, 2647–2659,
<a href="http://dx.doi.org/10.1016/0960-1686(92)90116-3" target="_blank">doi:10.1016/0960-1686(92)90116-3</a>, 1992.
</mixed-citation></ref-html>
<ref-html id="bib1.bib78"><label>78</label><mixed-citation>
Wu, Z. and Huang, N. E.: Ensemble Empirical Mode Decomposition: A
noise-assisted data analysis method, Advances in Adaptive Data Analysis, 01,
1–41, <a href="http://dx.doi.org/10.1142/S1793536909000047" target="_blank">doi:10.1142/S1793536909000047</a>, 2009.
</mixed-citation></ref-html>
<ref-html id="bib1.bib79"><label>79</label><mixed-citation>
Ziemke, J. R., Chandra, S., Oman, L. D., and Bhartia, P. K.: A new ENSO index
derived from satellite measurements of column ozone, Atmos. Chem. Phys., 10,
3711–3721, <a href="http://dx.doi.org/10.5194/acp-10-3711-2010" target="_blank">doi:10.5194/acp-10-3711-2010</a>, 2010.
</mixed-citation></ref-html>--></article>
