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  <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-20-3569-2020</article-id><title-group><article-title>Evaluating China's anthropogenic <inline-formula><mml:math id="M1" 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> emissions inventories: a northern
China case study using continuous surface<?xmltex \hack{\break}?> observations from 2005 to 2009</article-title><alt-title>Evaluating China's anthropogenic <inline-formula><mml:math id="M2" 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> emissions
inventories</alt-title>
      </title-group><?xmltex \runningtitle{Evaluating China's anthropogenic {$\chem{CO_{{2}}}$} emissions
inventories}?><?xmltex \runningauthor{A.~Dayalu et~al.}?>
      <contrib-group>
        <contrib contrib-type="author" corresp="yes" rid="aff1 aff8">
          <name><surname>Dayalu</surname><given-names>Archana</given-names></name>
          <email>adayalu@aer.com</email>
        <ext-link>https://orcid.org/0000-0001-8663-9646</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff2 aff3">
          <name><surname>Munger</surname><given-names>J. William</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-1042-8452</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff4 aff5">
          <name><surname>Wang</surname><given-names>Yuxuan</given-names></name>
          
        <ext-link>https://orcid.org/0000-0002-1649-6974</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff2 aff3">
          <name><surname>Wofsy</surname><given-names>Steven C.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff6">
          <name><surname>Zhao</surname><given-names>Yu</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff1">
          <name><surname>Nehrkorn</surname><given-names>Thomas</given-names></name>
          
        <ext-link>https://orcid.org/0000-0003-0637-3468</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>Nielsen</surname><given-names>Chris</given-names></name>
          
        <ext-link>https://orcid.org/0000-0001-8043-2409</ext-link></contrib>
        <contrib contrib-type="author" corresp="no" rid="aff3">
          <name><surname>McElroy</surname><given-names>Michael B.</given-names></name>
          
        </contrib>
        <contrib contrib-type="author" corresp="no" rid="aff7">
          <name><surname>Chang</surname><given-names>Rachel</given-names></name>
          
        <ext-link>https://orcid.org/0000-0003-2337-098X</ext-link></contrib>
        <aff id="aff1"><label>1</label><institution>Atmospheric and Environmental Research, Lexington, MA, USA</institution>
        </aff>
        <aff id="aff2"><label>2</label><institution>Earth and Planetary Sciences, Harvard University, Cambridge, MA, USA</institution>
        </aff>
        <aff id="aff3"><label>3</label><institution>School of Engineering and Applied Sciences, Harvard University,
Cambridge, MA, USA</institution>
        </aff>
        <aff id="aff4"><label>4</label><institution>Department of Earth and Atmospheric Sciences, University of Houston,
Houston, TX, USA</institution>
        </aff>
        <aff id="aff5"><label>5</label><institution>Department of Earth System Sciences, Tsinghua University, Beijing,
China</institution>
        </aff>
        <aff id="aff6"><label>6</label><institution>School of the Environment, Nanjing University, Nanjing, China</institution>
        </aff>
        <aff id="aff7"><label>7</label><institution>Department of Physics and Atmospheric Science, Dalhousie University,
Halifax, Canada</institution>
        </aff>
        <aff id="aff8"><label>a</label><institution>formerly at: Earth and Planetary Sciences, Harvard University, Cambridge,
MA, USA</institution>
        </aff>
      </contrib-group>
      <author-notes><corresp id="corr1">Archana Dayalu (adayalu@aer.com)</corresp></author-notes><pub-date><day>25</day><month>March</month><year>2020</year></pub-date>
      
      <volume>20</volume>
      <issue>6</issue>
      <fpage>3569</fpage><lpage>3588</lpage>
      <history>
        <date date-type="received"><day>25</day><month>July</month><year>2019</year></date>
           <date date-type="accepted"><day>26</day><month>February</month><year>2020</year></date>
           <date date-type="rev-recd"><day>14</day><month>February</month><year>2020</year></date>
           <date date-type="rev-request"><day>12</day><month>September</month><year>2019</year></date>
      </history>
      <permissions>
        <copyright-statement>Copyright: © 2020 </copyright-statement>
        <copyright-year>2020</copyright-year>
      <license license-type="open-access"><license-p>This work is licensed under the Creative Commons Attribution 4.0 International License. To view a copy of this licence, visit <ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</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><title>Abstract</title>
    <?pagebreak page3570?><p id="d1e226">China has pledged reduction of carbon dioxide (<inline-formula><mml:math id="M3" 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>)
emissions per unit of gross domestic product (GDP) by 60 %–65 % relative to 2005 levels,
and to peak carbon emissions overall by 2030. However, the lack of
observational data and disagreement among the many available
inventories makes it difficult for China to track progress toward
these goals and evaluate the efficacy of control measures. To
demonstrate the value of atmospheric observations for constraining
<inline-formula><mml:math id="M4" 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> inventories we track the ability of <inline-formula><mml:math id="M5" 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>
concentrations predicted from three different <inline-formula><mml:math id="M6" 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>
inventories to match a unique multi-year continuous record of
atmospheric <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>. Our analysis time window includes the key
commitment period for the Paris Agreement (2005) and the Beijing
Olympics (2008). One inventory is China-specific and two are spatial
subsets of global inventories. The inventories differ in spatial
resolution, basis in national or subnational statistics, and reliance
on global or China-specific emission factors. We use a unique set of
historical atmospheric observations from 2005 to 2009 to evaluate the
three <inline-formula><mml:math id="M8" 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> emissions inventories within China's heavily
industrialized and populated northern region accounting for
<inline-formula><mml:math id="M9" display="inline"><mml:mo>∼</mml:mo></mml:math></inline-formula>33 %–41 % of national emissions. Each anthropogenic
inventory is combined with estimates of biogenic <inline-formula><mml:math id="M10" 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> within
a high-resolution atmospheric transport framework to model the time
series of <inline-formula><mml:math id="M11" 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> observations. To convert the model–observation
mismatch from mixing ratio to mass emission rates we distribute it
over a region encompassing 90 % of the total surface influence in
seasonal (annual) averaged back-trajectory footprints (L_0.90
region). The L_0.90 region roughly corresponds to northern
China. Except for the peak growing season, where assessment of
anthropogenic emissions is entangled with the strong vegetation
signal, we find the China-specific inventory based on subnational data
and domestic field studies agrees significantly better with
observations than the global inventories at all timescales. Averaged
over the study time period, the unscaled China-specific inventory
reports substantially larger annual emissions for northern China
(30 %) and China as a whole (20 %) than the two unscaled
global inventories. Our results, exploiting a robust time series of
continuous observations, lend support to the rates and geographic
distribution in the China-specific inventory Though even long-term
observations at a single site reveal differences among inventories,
exploring inventory discrepancy over all of China requires a denser
observational network in future efforts to measure and verify
<inline-formula><mml:math id="M12" 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> emissions for China both regionally and nationally. We
find that carbon intensity in the northern China region has decreased
by 47 % from 2005 to 2009, from approximately
4 <inline-formula><mml:math id="M13" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi></mml:mrow></mml:math></inline-formula> of <inline-formula><mml:math id="M14" 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> per USD (note that all references to USD in this paper refer to USD adjusted for purchasing power parity, PPP) in 2005 to about
2 <inline-formula><mml:math id="M15" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi></mml:mrow></mml:math></inline-formula> of <inline-formula><mml:math id="M16" 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> per USD in 2009
(Fig. 9c). However, the corresponding 18 % increase in
absolute emissions over the same time period affirms a critical point
that carbon intensity targets in emerging economies can be at odds
with making real climate progress. Our results provide an important
quantification of model–observation mismatch, supporting the increased
use and development of China-specific inventories in tracking China's
progress as a whole towards reducing emissions. We emphasize that this
work presents a methodology for extending the analysis to other
inventories and is intended to be a comparison of a subset of
anthropogenic <inline-formula><mml:math id="M17" 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> emissions rates from inventories that were
readily available at the time this research began. For this study's
analysis time period, there was not enough spatially distinct
observational data to conduct an optimization of the inventories.  The
primary intent of the comparisons presented here is not to judge
specific inventories, but to demonstrate that even a single site with
a long record of high-time-resolution observations can identify major
differences among inventories that manifest as biases in the
model–data comparison. This study provides a baseline analysis for
evaluating emissions from a small but important region within China,
as well a guide for determining optimal locations for future
ground-based measurement sites.</p>
  </abstract>
    </article-meta>
  </front>
<body>
      

      <?xmltex \hack{\allowdisplaybreaks}?>
<sec id="Ch1.S1" sec-type="intro">
  <label>1</label><title>Introduction</title>
      <p id="d1e397">China's contribution to world <inline-formula><mml:math id="M18" 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> emissions has been
steadily growing, becoming the largest in the world in 2006. China has
accounted for 60 % of the overall growth in global <inline-formula><mml:math id="M19" 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>
emissions over the past 15 years (US EIA, 2017) Under the United Nations
Framework Convention on Climate Change (UNFCCC) 2015 Paris
Agreement, China has committed to reducing its carbon intensity
(<inline-formula><mml:math id="M20" 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> emissions per unit of gross domestic product, GDP) by 60 %–65 % relative
to the baseline year of 2005, and to peak carbon emissions overall by
or before 2030. Demonstration of progress on emissions reduction and
evaluation of how well specific policies are working is hindered by
large uncertainty in the existing Chinese emission inventories. In
2012 the discrepancy between data reported at national and provincial
levels was approximately half of China's 2020 emission reduction goals
(US EIA, 2017; NDRC, 2015; Guan et al., 2012; Zhao et al.,
2012). Moreover, China is under mounting pressure to address severe
regional air pollution events that are often associated with
<inline-formula><mml:math id="M21" 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> emissions sources – vehicles, power plants, and other
fossil-fuel-burning operations. China's 11th Five Year Plan (11th FYP)
of 2006–2010 included aggressive measures to retire inefficient
coal-fired power plants and improve energy efficiency in other
industries starting in 2007 (Zhao et al., 2013; Nielsen and Ho,
2013). A number of pollution control measures that were implemented
specifically in preparation for the 2008 Beijing Summer Olympics were
also largely in effect by the end of 2007 (Nielsen and Ho, 2013; Wang
et al., 2010).</p>
      <p id="d1e444">A variety of top-down approaches including inverse analysis (Le Quéré
et al., 2016) and comparison between atmospheric observations and
Eulerian forward model predictions (X. Wang et al., 2013) have been
used to evaluate and constrain emission estimates, albeit at coarse
spatial resolution. As noted by Wang et al. (2011) grid-based
atmospheric models have difficulty in simulating high-concentration
pollution plumes at specific receptor sites that are too near the
source region. The expanding network of high-accuracy <inline-formula><mml:math id="M22" 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>
observations coupled with high spatial resolution transport models is
emerging as a viable tool for evaluating high-resolution emission
inventories (e.g., Sargent et al., 2018). In this paper we adopt
a Lagrangian transport model to simulate atmospheric mixing and
transport. Continuous observations of <inline-formula><mml:math id="M23" 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> for the period
2005–2009 at Miyun, an atmospheric observatory about 100 <inline-formula><mml:math id="M24" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula> northeast of Beijing, provide a top-down constraint for evaluating persistent
bias among emissions rates obtained from a suite of three independent
anthropogenic emission inventories that were readily available as
spatially gridded fluxes.</p>
      <p id="d1e477">The three inventories that are evaluated span a range of bottom-up
inventory approaches. They are not intended to be an exhaustive set,
but are examples to demonstrate the capability to identify significant
differences in the ability of different inventories to match the long
time series of observations. Emerging inventory approaches based on
updated (yet non-China-specific) point-source data and
satellite observations of night lights as a proxy for spatial
allocation of energy production (Oda et al., 2018) were not readily
available when this analysis began. Two of the inventories, the
Emissions Database for Global Atmospheric Research (EDGAR; European Commission, Joint Research Centre/Netherlands Environmental
Assessment Agency, 2013) and Carbon Dioxide Information Analysis Center
(CDIAC), are spatial subsets from larger global models of
<inline-formula><mml:math id="M25" 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> emissions (European Commission, Joint Research Centre/Netherlands Environmental
Assessment Agency, 2013; Andres et al.,
2016a). They rely on
national-level energy statistics and global default values for
sectoral emission factors, and they estimate activity levels using
generalized proxies (e.g., population). The third inventory (ZHAO) is
specific to China, with greater reliance on energy statistics at
provincial and individual facility levels as well as emission factors
from domestic field studies (Zhao et al., 2012). The ZHAO inventory
was readily accessible at the time of this research and represents
increased efforts in recent years to incorporate more China-specific
data into emissions inventories. Other China-specific inventories that
have been recently developed but were not readily available at the
time of this research include the Multi-resolution Emissions Inventory
(MEIC, <uri>http://www.meicmodel.org/</uri>, last access: 12 April 2019) and an inventory by Shan
et al., 2016. The primary intent of the<?pagebreak page3571?> comparisons presented here is
not to judge specific inventories, but to demonstrate that even
a single site with a long record of high-time-resolution observations
can identify the potential impact of major differences among
inventories that manifest as biases in the model–data comparison.</p>
      <p id="d1e494">A study by Turnbull et al. (2011) used weekly flask observations to
evaluate a hybrid approach to inventory construction where CDIAC and
EDGAR estimates were spatially allocated to a provincial
emissions-based grid. However, to our knowledge, none of the truly
China-specific <inline-formula><mml:math id="M26" 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> inventories have been evaluated with
independent high-temporal-resolution atmospheric observations. The
official national total for China's 2005 <inline-formula><mml:math id="M27" 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> emissions from
energy-related activities, used as the benchmark for the Paris
commitment, is approximately 5.4 <inline-formula><mml:math id="M28" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">Gt</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> (NDRC,
2015). ZHAO, EDGAR, and the CDIAC national total (Boden et al., 2016)
report total 2005 energy-related <inline-formula><mml:math id="M30" 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> emissions that are
higher by 31 % (7.1 <inline-formula><mml:math id="M31" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">Gt</mml:mi></mml:mrow></mml:math></inline-formula>), 9 % (5.9 <inline-formula><mml:math id="M32" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">Gt</mml:mi></mml:mrow></mml:math></inline-formula>), and
7 % (5.8 <inline-formula><mml:math id="M33" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">Gt</mml:mi></mml:mrow></mml:math></inline-formula>), respectively. As the official national
total is not available in a spatially allocated format, it cannot be
tested by observations and we refer to it only as a benchmark in our
analysis. We will show that the China-specific inventory (ZHAO)
provides excellent agreement with observations, and markedly more so
than EDGAR and CDIAC. The result provides guidance for efforts to
assess China's emissions at larger scales as well as potential updates
for the Paris Agreement base-year emissions.</p>
      <p id="d1e575">In order to independently evaluate and scale existing bottom-up
estimates of China's <inline-formula><mml:math id="M34" 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> emissions, we employ a top-down
approach using 5 years of continuous <inline-formula><mml:math id="M35" 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>
observations. Modeled concentrations of <inline-formula><mml:math id="M36" 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> are obtained
from convolving hourly <inline-formula><mml:math id="M37" 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> surface flux estimates with
surface influence estimates (“footprints”) derived from the
Stochastic Time-Inverted Lagrangian Transport Model driven with
meteorology from the Weather Research and Forecasting Model version
3.6.1 (WRF-STILT; Lin et al., 2003; Nehrkorn et al., 2010). NOAA
CarbonTracker (CT2015) provides modeled estimates of advected upwind
background concentrations of <inline-formula><mml:math id="M38" 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> that are enhanced or
depleted by processes in the study region. As atmospheric
<inline-formula><mml:math id="M39" 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> concentrations are significantly modulated by
photosynthetic and respiratory fluxes, we additionally prescribe
hourly biosphere fluxes of <inline-formula><mml:math id="M40" 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> using data-driven outputs
from the Vegetation, Photosynthesis, and Respiration Model (VPRM)
adapted for China (Mahadevan et al., 2008; Dayalu et al., 2018a). VPRM
provides a functional representation of biosphere fluxes based on data
from remote sensing platforms and eddy flux towers, with significantly
better observationally validated performance relative to subsets of
global vegetation models (Dayalu et al., 2018a). The WRF-STILT-VPRM
framework has been successfully adapted for similar emissions
evaluation studies in North America in regions where biogenic fluxes
dominate surface processes (e.g., Sargent et al., 2018; Karion et al.,
2016; Matross et al., 2006). For the northern China region,
anthropogenic fluxes exceed biogenic fluxes for all but the peak of
growing season, when they are roughly comparable (Dayalu et al.,
2018a), which reduces the magnitude of overall error from incorrect
modeling of the biosphere. In contrast to extensive measurement
networks that exist in North America, continuous high-temporal-resolution measurements of <inline-formula><mml:math id="M41" 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> necessary for inventory
evaluation applications are sparse and very few datasets are available
in China (Wang et al., 2010). Despite this limitation, our site
provides valuable information and constraints on emissions
inventories: the long time series and spatial sampling heterogeneities,
where the site receives both clean continental air as well as air from
one of the heaviest emitting regions of China, present a powerful and
unique dataset for the region. Our inventory scaling is confined to
the northern China region, but this region accounts for
33 %–41 % of China's total annual <inline-formula><mml:math id="M42" 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> emissions
from fossil-fuel combustion. Model–observation mismatches can be
converted from concentration units (ppm) to mass units (Mt
<inline-formula><mml:math id="M43" 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>) across the most relevant area subset from modeled
annual average surface sensitivity footprints (ppm <inline-formula><mml:math id="M44" 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="M45" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">µ</mml:mi></mml:mrow></mml:math></inline-formula>mol<inline-formula><mml:math id="M46" display="inline"><mml:msup><mml:mi/><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup></mml:math></inline-formula> <inline-formula><mml:math id="M47" 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> m<inline-formula><mml:math id="M48" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:math></inline-formula> s). Ultimately, we compare the inventories by
quantifying model–observation mismatch for seasons (using additive
mass units) and annually (using scaling factors). We note that
identical transport fields and modeled biogenic fluxes are applied to
all the anthropogenic emission fields. Unresolved transport error and
error in biogenic fluxes undoubtedly contributes to scatter in the
model–data comparison. While random transport errors are unlikely to
generate consistent biases among the inventories, systematic transport
errors can be attributed to biases among inventories with differing
spatial allocations.  Although the interaction of systematic transport
errors with differences in spatial distribution could bias individual
observations, averaging over longer timescales (seasons, years)
minimizes the bias of individual points.  With the available
observational data it is not possible to evaluate the error in spatial
allocation of individual emissions inventories. For example, future
access to total column measurements and/or aircraft vertical profiles
would provide additional constraints on spatial allocations of sources
and sinks.</p>
      <p id="d1e741">Section 2 of this paper describes the observational <inline-formula><mml:math id="M49" 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 used in this analysis. Section 3 details the analysis methods,
including WRF-STILT model configuration, a discussion of the main
features of the inventories, error evaluation, and inventory scaling
methods. We present the results in Sect. 4, beginning with an
assessment of seasonality impacts. We then compare inventory
performance against observations across multiple timescales from
hourly to annual. We conclude Sect. 4 with scaling results, and
a brief examination of regional carbon intensity over the study
period.  Concluding remarks are provided in Sect. 5. Additional
methodological details are provided in the accompanying Supplement
and at <ext-link xlink:href="https://doi.org/10.7910/DVN/OJESO0" ext-link-type="DOI">10.7910/DVN/OJESO0</ext-link>.</p>
</sec>
<?pagebreak page3572?><sec id="Ch1.S2">
  <label>2</label><?xmltex \opttitle{{$\protect\chem{CO_{{2}}}$} observations}?><title><inline-formula><mml:math id="M50" 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> observations</title>
      <p id="d1e777">This study uses 5 years (2005–2009) of continuous hourly averaged
<inline-formula><mml:math id="M51" 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> observations (LI-COR Biosciences Li-7000; <inline-formula><mml:math id="M52" display="inline"><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mi mathvariant="italic">σ</mml:mi></mml:mrow></mml:math></inline-formula>
analytical precision of 0.08 <inline-formula><mml:math id="M53" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>), measured at a site in
northern China (Miyun; 40<inline-formula><mml:math id="M54" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>29<inline-formula><mml:math id="M55" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> N,
116<inline-formula><mml:math id="M56" display="inline"><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:math></inline-formula>46.45<inline-formula><mml:math id="M57" display="inline"><mml:msup><mml:mi/><mml:mo>′</mml:mo></mml:msup></mml:math></inline-formula> E). The Miyun receptor is an atmospheric
measurement station in a rural site 100 <inline-formula><mml:math id="M58" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula> northeast of the
Beijing urban center (Fig. S2 in the Supplement). It was established in 2004 by
collaborating researchers at the Harvard China Project and operated by
researchers at Tsinghua University. The site is strategically located
to capture both clean continental background air from the
west and northwest and polluted air from the Beijing region to the
southwest. Miyun is located south of the foothills of the Yan
mountains; the region consists of grasslands, small-scale agriculture
intermingled with rural villages and manufacturing complexes, and
mixed temperate forest. Land use varies from rural to suburban and
dense urban to the south towards Beijing center and sparsely populated
and wooded mountains to the north and west. Further descriptions of
the site and details of the instrumentation including calibration
strategy and assessment of long-term drifts are provided in Wang
et al. (2010). Average annual data coverage (based on hourly data)
over the study time period was 83 % (range: 78 % to 92 %).</p>
</sec>
<sec id="Ch1.S3">
  <label>3</label><title>Methods</title>
      <p id="d1e862">We evaluate the performance of the ZHAO, EDGAR, and CDIAC inventories
coupled with biogenic fluxes by modeling 5 years of hourly
<inline-formula><mml:math id="M59" 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> observations using the Stochastic Time-Inverted
Lagrangian Transport Model (STILT; Lin et al., 2003) run in backward
time mode driven by high-resolution meteorology from the Weather
Research and Forecasting Model version 3.6.1 (WRF). The WRF-STILT tool
models the surfaces that influenced each measurement hour in the study
domain (Fig. 1). Hourly vegetation <inline-formula><mml:math id="M60" 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> fluxes are prescribed
by the VPRM adapted for China (Mahadevan et al., 2008; Dayalu et al.,
2018a). We categorize seasons by months based on regional growing
season patterns, which are heavily dominated by winter wheat and corn
dual-cropping regions in the North China Plain (Dayalu et al.,
2018a). Winter wheat emergence in the spring and corn emergence in
later summer shift the seasonal patterns such that regional seasons
are more appropriately represented as January, February, March
(JFM, winter); April, May, June (AMJ, spring); July, August, September
(JAS, summer); and October, November, December (OND, fall).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F1"><?xmltex \currentcnt{1}?><label>Figure 1</label><caption><p id="d1e889">Study domain configuration. Miyun receptor and Beijing center are
located within the innermost domain at a resolution of 3 <inline-formula><mml:math id="M61" display="inline"><mml:mo>×</mml:mo></mml:math></inline-formula> 3 <inline-formula><mml:math id="M62" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula>. NOAA ESRL/WMO (WMO) flask sampling sites used to evaluate bias in CT2015 modeled backgrounds are the solid shapes; nearest CT2015 comparison pixel is the corresponding unfilled shape.</p></caption>
        <?xmltex \igopts{width=236.157874pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f01.png"/>

      </fig>

      <p id="d1e913">Ultimately, modeled concentrations of <inline-formula><mml:math id="M63" 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> are obtained from
convolving hourly surface flux estimates with footprints derived from
the WRF-STILT framework. NOAA CarbonTracker (CT2015) provides
estimates of advected upwind background concentrations of
<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> that are enhanced or depleted by processes in the study
region. Our final model–measurement dataset is the subset
consisting of local daytime values (hourly data from 11:00 to 16:00 LT).  Of this subset, only individual hours for which
observational data exist (i.e., non-missing data) are included. The
final dataset was further filtered to include only CT2015 background
values satisfying true background criteria as described in Sect. 3.4
and in Sect. S4 in the Supplement. As is typical for studies of this
nature, our analysis focuses on observations during the 11:00 to
16:00 LT period. The stronger vertical mixing in the daytime
atmosphere (notably absent at night) reduces the influence of
extremely local emissions. We select the 11:00–16:00 window to avoid
the presence of shallow inversion layers that are poorly represented
in STILT and use the period when vertical mixing through the entire
boundary layer is at its maximum (McKain et al., 2015; Sargent et al.,
2018). We adjust fluxes based on model–measurement mismatch of this
final data subset, focusing on the region that our model finds to be the most
influential to the signal measured at the receptor. Method details and
model components are described individually below.</p>
<sec id="Ch1.S3.SS1">
  <label>3.1</label><title>WRF-STILT model configuration</title>
      <p id="d1e946">The WRF-STILT particle transport framework and optimal configuration
have been extensively tested in several studies using midlatitude
receptors (e.g., Sargent et al., 2018; McKain et al., 2015; Kort
et al., 2013; McKain et al., 2012; Miller et al., 2012). WRF is
configured with 41<?pagebreak page3573?> vertical levels and two-way nesting in three
domains, with the outermost domain covering nearly seven
administrative regions (Figs. 1 and 2), defined according to
convention in Piao et al. (2009). The domain resolutions from coarsest
to finest are 27 <inline-formula><mml:math id="M65" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula> (d01), 9 <inline-formula><mml:math id="M66" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula> (d02), and
3 <inline-formula><mml:math id="M67" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula> (d03). Initial and lateral WRF boundary conditions are
provided by NCEP FNL Operational Model Global Tropospheric Analyses at
<inline-formula><mml:math id="M68" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> spatial 6-hourly temporal resolution (NCEP,
1999). Nudging of fields is implemented in the outer domain only, and
never within the planetary boundary layer (PBL). WRF output is
evaluated against publicly accessible 24-hourly averaged observational
datasets from the Chinese Meteorological Administration (CMA); finer
temporal resolution meteorological data are not publicly available. WRF
run details are presented in Dayalu (2017) and at
<ext-link xlink:href="https://doi.org/10.7910/DVN/OJESO0" ext-link-type="DOI">10.7910/DVN/OJESO0</ext-link>. A snapshot of results from
comparison with China Meteorological Administration ground-station
measurements is presented Sect. S1 and Figs. S1–S4 in the Supplement.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F2" specific-use="star"><?xmltex \currentcnt{2}?><label>Figure 2</label><caption><p id="d1e998">2005–2009 mean seasonal <bold>(a–d)</bold> and Annual <bold>(e)</bold> footprint contours, as percentiles of influence highlighted by administrative region.  Red, blue, and black contour lines represent 50th, 75th, and 90th percentile regions, respectively. Stippling represents location of <inline-formula><mml:math id="M69" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> footprint and inventory grid cell centers, colored by relevant administrative regions. Northern China (red stippling) is the administrative region with predominant influence on Miyun observations, followed by Inner Mongolia and northeastern China. Southeastern and central China have minimal representation, and only during the spring and summer seasons</p></caption>
          <?xmltex \igopts{width=426.791339pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f02.png"/>

        </fig>

      <p id="d1e1033">The STILT model is configured in backward time mode. The particle
release point is set as the Miyun measurement sample inlet (the
receptor). The inlet height is 158 <inline-formula><mml:math id="M70" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">m</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mi mathvariant="normal">a</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">s</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">l</mml:mi><mml:mo>.</mml:mo></mml:mrow></mml:math></inline-formula>, corresponding to
6 <inline-formula><mml:math id="M71" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">m</mml:mi><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mi mathvariant="normal">a</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">g</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">l</mml:mi><mml:mo>.</mml:mo></mml:mrow></mml:math></inline-formula> In our study, the hilltop site was located in an
area where the surrounding land was not very productive or intensively
cultivated (Fig. S2). There is a long history of using
short towers in low-productivity areas for regional studies (e.g., NOAA
Earth Systems Research Laboratory – NOAA ESRL Barrow, Alaska,
observatory at 11 <inline-formula><mml:math id="M72" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">m</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="normal">a</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">g</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">l</mml:mi><mml:mo>.</mml:mo></mml:mrow></mml:math></inline-formula>). In addition, the station is
located on a small hilltop, so even though the actual inlet height
above ground is low, it has a topographic advantage in that it
effectively samples air from a greater height relative to the
surroundings.  Topographic advantage was exploited in a similar manner
in Karion et al. (2016) in the context of an Alaskan <inline-formula><mml:math id="M73" 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>
study. However, Karion et al. (2016) were able to use a suite of
additional data to confirm the validity of their assumption including
comparisons to concurrent aircraft measurements and multiple inlets at
31.7, 17.1, and 4.9 <inline-formula><mml:math id="M74" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">m</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="normal">a</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">g</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">l</mml:mi><mml:mo>.</mml:mo></mml:mrow></mml:math></inline-formula> In our study, independent
verification from concurrent aircraft measurements (for example) or
multi-level inlet locations were not available to quantify the impact
of absolute and relative inlet location on transport uncertainty.</p>
      <p id="d1e1132">Each hourly footprint (<inline-formula><mml:math id="M75" 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> concentration attributed to each
unit of flux as <inline-formula><mml:math id="M76" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="normal">µ</mml:mi><mml:msup><mml:mi mathvariant="normal">mol</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:msup><mml:mspace linebreak="nobreak" width="0.125em"/><mml:msup><mml:mi mathvariant="normal">m</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:mrow></mml:math></inline-formula>) provides an
estimate of surface influence on the measurement and is calculated
from releasing 500 particles from the measurement site (receptor)
until they reach the outer domain boundaries up to 7 d back in
time. The STILT <inline-formula><mml:math id="M77" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> footprint map for each
measurement hour up to 7 d back in time enables assessment of
regions in the study domain to which the receptor is most
sensitive. These entire gridded footprints are convolved with
anthropogenic and biogenic <inline-formula><mml:math id="M78" 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> flux estimates to provide
a final modeled concentration (ppm) of <inline-formula><mml:math id="M79" 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> at the
receptor. For clarity, we display the regions of importance to the
receptor based on contours calculated from the overall STILT
footprints at the 50th (L_0.50 region), 75th (L_0.75
region), and 90th (L_0.90 region) percentile levels (Fig. 2). The
percentile contours are calculated as follows: the average (seasonal,
annual) footprints from 2005 to 2009 are ordered from high to low. We
multiply each fraction (0.5, 0.75, 0.9) with the summed footprints and
use cumulative sums of the ordered footprints as a guide to select all
points with influence magnitude equal to or greater than this cutoff
value.  Figure S11 illustrates a single footprint map along
with the average influence and a plot of cumulative influence to
demonstrate the percentile-level selection process. We emphasize that
we use the entire STILT footprint convolved with fluxes to estimate
the receptor <inline-formula><mml:math id="M80" 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> concentration. We only use the L_0.90
region to provide a reasonable area across which to ascribe the
effective inventory adjustment (converted from parts per million model–observation
mismatch to mass units). As Fig. S11c shows, the L_0.90
region strikes a balance between capturing sufficient influence while
avoiding an unrealistically large adjustment region for a single
observation site. Conversely, corrections based on the smaller
L_0.75 region would include larger uncertainties from the diffuse
influence of emissions outside the L_0.75 region (not accounting
for 25 % of average surface sensitivity), yet the
model–observation mismatch would be ascribed to a region approximately
half the area of the L_0.90 region. Deriving correction factors
based on integration over the entire L_0.90 region is a more
conservative approach where the model–observation mismatch in mass
units is distributed over a larger area.</p>
      <p id="d1e1228">Further model details are available in
Sect. S2. Complete WRF-STILT settings and STILT footprint files are
available from <ext-link xlink:href="https://doi.org/10.7910/DVN/OJESO0" ext-link-type="DOI">10.7910/DVN/OJESO0</ext-link>.</p>
</sec>
<sec id="Ch1.S3.SS2">
  <label>3.2</label><?xmltex \opttitle{Anthropogenic {$\protect\chem{CO_{{2}}}$} emissions inventories}?><title>Anthropogenic <inline-formula><mml:math id="M81" 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> emissions inventories</title>
      <p id="d1e1254">ZHAO, EDGAR, and CDIAC report estimates of total annual emissions of
<inline-formula><mml:math id="M82" 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> at <inline-formula><mml:math id="M83" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M84" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula>, and <inline-formula><mml:math id="M85" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> original grid resolutions,
respectively. We regridded the EDGAR and CDIAC inventories to the
<inline-formula><mml:math id="M86" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> resolution, using the NCAR Command Language
version 6.2.1 Earth System Modeling Framework “conserve” regridding
algorithm to preserve the integral of emissions (Brown et al.,
2012). Differences between annual total emissions for EDGAR and CDIAC
inventories introduced by regridding are smaller than the interannual
trends or differences between the inventories (Sect. S3 and
Fig. S5). We present the main components and defining features of the
three anthropogenic <inline-formula><mml:math id="M87" 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> inventories below.</p>
      <p id="d1e1360">The ZHAO inventory provides estimates of total annual emissions for
2005 through 2009. In addition, the spatial location of emissions is given
for years 2005 and 2009 on a <inline-formula><mml:math id="M88" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula>
grid. Using 2005 and 2009 gridded values, we calculate an
average percent contribution of each grid cell to the total
emissions. The average contributions are used as weights to spatially
allocate 2006, 2007, and 2008 total<?pagebreak page3574?> annual emissions. We evaluate and
justify this assumption in detail in  Sect. S3 and
Fig. S6. The ZHAO inventory represents one of the first statistically
rigorous bottom-up <inline-formula><mml:math id="M89" 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> inventories for China. It relies on
provincial- and facility-level data rather than national-level data,
which has been noted previously as a major uncertainty in Chinese
emission inventories; total <inline-formula><mml:math id="M90" 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> emissions estimates based on
provincial data are typically higher than those using national
statistics (Zhao et al., 2013). Satellite observations of criteria air
pollutants (e.g., nitrogen dioxide, which serves as a proxy for fossil
fuel combustion) show greater agreement with provincial statistics
(Zhao et al., 2012). The increased use of China-specific emission
factors and activity levels based on domestic field studies is a shift
from other inventories that rely heavily on global averages to
estimate processes occurring in China. Despite the increased
incorporation of China-specific field data, the largest sources of
uncertainty to the ZHAO inventory are industrial emission factors, and
activity levels across all sectors. Total uncertainty in the inventory
is estimated as <inline-formula><mml:math id="M91" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">9</mml:mn></mml:mrow></mml:math></inline-formula> % to <inline-formula><mml:math id="M92" display="inline"><mml:mrow><mml:mo>+</mml:mo><mml:mn mathvariant="normal">11</mml:mn></mml:mrow></mml:math></inline-formula> % (Zhao et al., 2012).</p>
      <p id="d1e1425">The EDGAR emissions database continues to be a major prior in
atmospheric studies, and the <inline-formula><mml:math id="M93" 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> inventory is used to inform
key global scientific results considered by the UNFCCC Conference of
Parties. The EDGAR global inventory (atemporal EDGAR v4.2 FT2010
gridded emissions) takes total annual estimates of national emissions
and downscales emissions to a <inline-formula><mml:math id="M94" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> as
a function of road and shipping networks, population density,
energy and manufacturing point sources, and agricultural land. Estimates
for China are available for all 5 years as gridded
inventories. Reported uncertainties for global emissions are <inline-formula><mml:math id="M95" display="inline"><mml:mrow><mml:mo>±</mml:mo><mml:mn mathvariant="normal">10</mml:mn></mml:mrow></mml:math></inline-formula> % (<uri>https://themasites.pbl.nl/tridion/en/themasites/edgar/documentation/uncertainties/index-2.html</uri>, last access: 10 February 2020).
However, this applies to global averaged uncertainty; we expect
uncertainty for China to be much higher.</p>
      <p id="d1e1473">We include the CDIAC inventory here due to its historical prevalence
as a benchmark inventory for global indicators, including evaluations
of carbon intensity provided by the World Bank (World Bank, 2017). The
CDIAC inventory (v2016;
<ext-link xlink:href="https://doi.org/10.3334/CDIAC/ffe.ndp058.2016" ext-link-type="DOI">10.3334/CDIAC/ffe.ndp058.2016</ext-link>) allocates estimates
of national emissions to a <inline-formula><mml:math id="M96" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">1</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> grid,
primarily distributed according to human population
density. A thorough assessment of <inline-formula><mml:math id="M97" display="inline"><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mi mathvariant="italic">σ</mml:mi></mml:mrow></mml:math></inline-formula> uncertainties in the
CDIAC spatial allocation of emissions shows considerable spread in
regional uncertainties (Andres et al., 2016).</p>
      <p id="d1e1509">Our study is not intended to be an exhaustive sampling of inventory
approaches but serves to demonstrate the<?pagebreak page3575?> utility of continuous
high-accuracy observations as a top-down constraint on emissions
evaluations. Our inventory list notably does not include emerging
spatially resolved global inventories (e.g., Open Data Inventory for
Anthropogenic Carbon Dioxide, ODIAC) (Oda et al., 2018) that were not
readily available at the time this work was conducted. At <inline-formula><mml:math id="M98" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mo>×</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M99" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">km</mml:mi></mml:mrow></mml:math></inline-formula>, ODIAC does have a high spatial resolution of
nightlight proxy-based emissions; while this is a valuable method for
regions in Europe and North America for example, it is less valuable
for China where it is analogous to the CDIAC population-based
proxy. In China, power plant emissions are typically located far from
end-use regions and the night-light proxy can often break down (R. Wang
et al., 2013). Furthermore, ODIAC power plant emissions use the
2012 Carbon Monitoring for Action (CARMA) database, which notably does
not incorporate China-specific power plant data; in these instances,
CARMA categorizes China's power plants as “non-disclosed plants” and
reports using estimates derived from statistical models using averaged
emissions factors – comparable to methods in global inventories
subset over China (Ummel, 2012).  One of our main goals is to quantify
model–observation mismatch associated with use of China-specific power
plant data, and ODIAC does not address that issue particularly
differently from other global emissions inventories subset over
China. For completeness, however, evaluation of global inventories
like ODIAC and a suite of increasingly available China-specific
inventories (e.g., MEIC) would provide value as part of future
model–observation comparison efforts.</p>
      <p id="d1e1532">Based on multi-year means (2005 to 2009) and 95 % confidence
intervals derived from two-sample <inline-formula><mml:math id="M100" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> tests, we find that within the
L_0.90 evaluation region EDGAR and CDIAC report emissions that are
significantly lower than ZHAO by typically 20 % (<inline-formula><mml:math id="M101" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">24</mml:mn></mml:mrow></mml:math></inline-formula> %,
<inline-formula><mml:math id="M102" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">16</mml:mn></mml:mrow></mml:math></inline-formula> %) and 36 % (<inline-formula><mml:math id="M103" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">37</mml:mn></mml:mrow></mml:math></inline-formula> %, <inline-formula><mml:math id="M104" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">34</mml:mn></mml:mrow></mml:math></inline-formula> %),
respectively. Across China's administrative regions, the highest
discrepancy between the global and regional inventories is in northern
China (ZHAO is approximately 30 % higher than both EDGAR and
CDIAC). In addition, northern China represents one of the
administrative regions with the highest <inline-formula><mml:math id="M105" 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> emissions
density (2300 to 3300 <inline-formula><mml:math id="M106" display="inline"><mml:mrow class="unit"><mml:msub><mml:mi mathvariant="normal">MgCO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">km</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>,
compared to the average of 700 <inline-formula><mml:math id="M107" display="inline"><mml:mrow class="unit"><mml:msub><mml:mi mathvariant="normal">MgCO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">km</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula>
averaged across China) and is therefore a particularly rich spatial
subset for emissions inventory evaluation. A detailed breakdown of
emissions by region of China is provided ins Table S1 in the Supplement. Spatial differences are displayed in  Fig. S7.</p>
      <p id="d1e1634">Previous work has found that temporal variations in <inline-formula><mml:math id="M108" 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>
sources can be significant and surface <inline-formula><mml:math id="M109" 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> can be perturbed
by between 1.5 and 8 <inline-formula><mml:math id="M110" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula> within source regions based on the time of day
and/or day of week, resulting from a combination of changes in
activity patterns as well as synoptic-scale transport effects (Nassar
et al., 2013). However, appropriate data for establishing reasonable
temporal scaling factors for data-sparse regions such as China are
difficult to obtain, and as in the case of Nassar et al. (2013)
China's activity factors are based on US activity factors weighted
according to China's EDGARv4.2 emissions patterns. We applied the
weekly and diurnal Nassar et al. (2013) scaling factors to our
emissions, but these did not generate statistically significant
differences from the unscaled versions. These statistically
insignificant results suggest that a more rigorous set of temporal
scaling factors need to be developed for China. CDIAC does provide
monthly gridded inventories with seasonality embedded. However,
predictions based on that seasonality deviated even further from the
observations than predictions based on constant annual emissions. In
the CDIAC global dataset, the seasonality in emissions is based upon
generalized global activity factors that are not necessarily
appropriate for estimating seasonality of human activity in China.
Therefore, in this study we do not explicitly consider diel and
seasonal variation in anthropogenic <inline-formula><mml:math id="M111" 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> fluxes.</p>
</sec>
<sec id="Ch1.S3.SS3">
  <label>3.3</label><title>Vegetation flux inventory</title>
      <p id="d1e1686">We prescribe biotic contributions to the <inline-formula><mml:math id="M112" 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> signal by
adapting the VPRM model output for the study domain to generate
<inline-formula><mml:math id="M113" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">0.25</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula>  gridded estimates of hourly
<inline-formula><mml:math id="M114" 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> net ecosystem exchange (NEE) from 2005 to
2009. Details of the VPRM model and output for China are presented in
Dayalu et al. (2018a). The VPRM is driven by 8 d 500 <inline-formula><mml:math id="M115" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">m</mml:mi></mml:mrow></mml:math></inline-formula> MODIS
surface reflectance values and 10 <inline-formula><mml:math id="M116" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">min</mml:mi></mml:mrow></mml:math></inline-formula> averages of WRF downward
shortwave radiation and surface temperature fields. The VPRM
parameters are calibrated using eddy flux measurements in the study
domain representing each ecosystem type classified according to the
International Geosphere-Biosphere Programme (IGBP) scheme. Calibration
and evaluation eddy-flux data are obtained from FluxNet and ChinaFlux
collaborators. The L_0.90 region is dominated by croplands
(Fig. S8), in particular the winter wheat and corn dual cropping that
characterizes the North China Plain (Dayalu et al., 2018a). We use one
biosphere model in this study to simplify our assessment of variations
across the different emissions inventories. Our selection of the VPRM
in particular is based on results from Dayalu et al. (2018a), where the
VPRM was shown to have significantly lower regional bias than an
ensemble of global 3-hourly flux products subset over China.</p>
</sec>
<sec id="Ch1.S3.SS4">
  <label>3.4</label><title>Background concentrations</title>
      <p id="d1e1755">Appropriate quantification of background <inline-formula><mml:math id="M117" 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> concentrations
(i.e., the <inline-formula><mml:math id="M118" 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> concentration at the lateral edges of the
model domain and/or prior to interaction with domain surface
processes) enables realistic assessment of the study domain's
contribution to atmospheric <inline-formula><mml:math id="M119" 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> at varying
timescales. CT2015 estimates of <inline-formula><mml:math id="M120" 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> concentrations are
provided on a <inline-formula><mml:math id="M121" display="inline"><mml:mrow><mml:mn mathvariant="normal">3</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup><mml:mo>×</mml:mo><mml:mn mathvariant="normal">2</mml:mn><mml:msup><mml:mi/><mml:mo>∘</mml:mo></mml:msup></mml:mrow></mml:math></inline-formula> grid at upwind background
locations.  Background values are selected and corrected for
large-scale biases using methodology similar to Karion et al. (2016)
where a particle must originate from the outermost domain edge and/or
3000 <inline-formula><mml:math id="M122" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">m</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mi mathvariant="normal">a</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">s</mml:mi><mml:mo>.</mml:mo><mml:mi mathvariant="normal">l</mml:mi><mml:mo>.</mml:mo></mml:mrow></mml:math></inline-formula>; further details are provided in
Sect. S4. The predicted background <inline-formula><mml:math id="M123" 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> is shown in Fig. 3a together
with observed <inline-formula><mml:math id="M124" 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> at Miyun for the 11:00–16:00<?pagebreak page3576?> LT
period over the 5-year observational record. For most of the
year the measured <inline-formula><mml:math id="M125" 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> shows large enhancements above
background and only in midsummer is there a small depletion relative
to background values.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F3" specific-use="star"><?xmltex \currentcnt{3}?><label>Figure 3</label><caption><p id="d1e1879">Hourly (11:00 to 16:00 LT) modeled and measured <inline-formula><mml:math id="M126" 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="M127" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M128" 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>. Measured <inline-formula><mml:math id="M129" 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 modeled CT2015 background concentrations are displayed in <bold>(a)</bold>. Modeled versus measured <inline-formula><mml:math id="M130" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M131" 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> for each anthropogenic inventory is shown in <bold>(b)</bold>–<bold>(d)</bold>, colored by season. Histograms of modeled and measured residuals are shown in <bold>(e)</bold>–<bold>(g)</bold>. The VPRM vegetation component is included in all modeled <inline-formula><mml:math id="M132" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M133" 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> values.</p></caption>
          <?xmltex \igopts{width=398.338583pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f03.png"/>

        </fig>

</sec>
<sec id="Ch1.S3.SS5">
  <label>3.5</label><?xmltex \opttitle{Quantifying regional changes to background {$\protect\chem{CO_{{2}}}$} concentrations:
$\Delta${$\protect\chem{CO_{{2}}}$}}?><title>Quantifying regional changes to background <inline-formula><mml:math id="M134" 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> concentrations:
<inline-formula><mml:math id="M135" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M136" 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></title>
      <p id="d1e2014">We define hourly <inline-formula><mml:math id="M137" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M138" 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> as a regional change
(enhancement or depletion) imparted to concentrations of <inline-formula><mml:math id="M139" 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>
advected from the boundary (<inline-formula><mml:math id="M140" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CT</mml:mi><mml:mn mathvariant="normal">2015</mml:mn></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>) such that, for each
observation hour <inline-formula><mml:math id="M141" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula>,

                <disp-formula id="Ch1.E1" content-type="numbered"><label>1</label><mml:math id="M142" display="block"><mml:mrow><mml:mstyle class="stylechange" displaystyle="true"/><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>=</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>-</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CT</mml:mi><mml:mn mathvariant="normal">2015</mml:mn></mml:mrow></mml:msub></mml:mrow><mml:mo>.</mml:mo></mml:mrow></mml:math></disp-formula>

          For each modeled hour <inline-formula><mml:math id="M143" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">mod</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M144" display="inline"><mml:mi>i</mml:mi></mml:math></inline-formula> and <inline-formula><mml:math id="M145" display="inline"><mml:mi>j</mml:mi></mml:math></inline-formula> represent the surface grid cell locations and h represents the hour
of the 7 d back trajectory:

                <disp-formula id="Ch1.E2" content-type="numbered"><label>2</label><mml:math id="M146" display="block"><mml:mrow><mml:mstyle displaystyle="true" class="stylechange"/><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">mod</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>=</mml:mo><mml:munderover><mml:mo movablelimits="false">∑</mml:mo><mml:mrow><mml:mn mathvariant="normal">0</mml:mn><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mrow class="unit"><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">168</mml:mn><mml:mspace linebreak="nobreak" width="0.125em"/><mml:mrow class="unit"><mml:mi mathvariant="normal">h</mml:mi></mml:mrow></mml:mrow></mml:munderover><mml:munder><mml:mo movablelimits="false">∑</mml:mo><mml:mrow><mml:mi>i</mml:mi><mml:mi>j</mml:mi></mml:mrow></mml:munder><mml:msub><mml:mtext>foot</mml:mtext><mml:mrow><mml:mi>i</mml:mi><mml:mi>j</mml:mi></mml:mrow></mml:msub><mml:mspace width="0.125em" linebreak="nobreak"/><mml:mo>×</mml:mo><mml:mo>(</mml:mo><mml:msub><mml:mtext>ANTH</mml:mtext><mml:mrow><mml:mi>i</mml:mi><mml:mi>j</mml:mi></mml:mrow></mml:msub><mml:mo>+</mml:mo><mml:msub><mml:mtext>VPRM</mml:mtext><mml:mrow><mml:mi>i</mml:mi><mml:mi>j</mml:mi></mml:mrow></mml:msub><mml:mo>)</mml:mo><mml:mo>.</mml:mo></mml:mrow></mml:math></disp-formula>

          Note that for the modeled enhancement or depletion, only the VPRM
fluxes change hourly; as stated previously, the annual anthropogenic
fluxes are atemporal.</p>
      <p id="d1e2251">Without a sufficiently dense network of high-temporal-resolution
observations, a full-scale inverse modeling approach to inventory
scaling is inappropriate. At annual timescales, where anthropogenic
sources dominate the <inline-formula><mml:math id="M147" 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> signal, we compare annual observed
and modeled <inline-formula><mml:math id="M148" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M149" 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> to define a mean bias and derive
a scale factor to quantify the model–observation mismatch based on the
slope of the comparison. Isotopic analysis of atmospheric
<inline-formula><mml:math id="M150" 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> from a site in Beijing in 2014 suggests that annually
the fossil fuel burning does dominate the region, contributing
75 % <inline-formula><mml:math id="M151" display="inline"><mml:mo>±</mml:mo></mml:math></inline-formula> 15 % to the annual signal (Niu et al.,
2016). Annually, the biospheric impact in the region is not zero;
rather, the anthropogenic signal dominates. The biospheric quantity of
relevance annually is the net carbon flux as a balance of GPP and
respiration and is highly uncertain in both sign and magnitude in
this region (Piao et al., 2009). In the Piao et al. (2009) study,
regional inversions are based on the very limited dataset of nine
sites across all of Asia. Our assumption of dominant anthropogenic
influence in northern China is in keeping with the priors and
process-based models from the relevant regions in Piao et al. (2009)
that assume zero and are not significantly corrected by relatively
poorly constrained inversions.  At seasonal timescales, we use the
difference between observed and modeled <inline-formula><mml:math id="M152" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M153" 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>
normalized by L_0.90 area to obtain a mass flux offset that
combines vegetation and anthropogenic inventories. With the available
data it is not possible to independently evaluate both the
anthropogenic and biogenic <inline-formula><mml:math id="M154" 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> fluxes. For further details
of the scaling technique, please refer to  Sect. S5.</p><?xmltex \hack{\newpage}?>
<sec id="Ch1.S3.SS5.SSSx1" specific-use="unnumbered">
  <title>Uncertainty analysis</title>
      <p id="d1e2335">The sources of uncertainty in calculations of <inline-formula><mml:math id="M155" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M156" 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>
include uncertainty in CT2015 background concentrations, <inline-formula><mml:math id="M157" 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>
observations, STILT footprints, anthropogenic inventories, and the
biogenic <inline-formula><mml:math id="M158" 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> fluxes from the VPRM. We obtain 95 %
confidence bounds for <inline-formula><mml:math id="M159" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M160" 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> by following a procedure
similar to McKain et al. (2015) and Sargent et al. (2018) that
involves bootstrapping daily averages of hourly afternoon values. For
monthly and seasonal timescales, we obtain 95 % confidence
intervals for <inline-formula><mml:math id="M161" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> by performing a bootstrap
on probability distributions of errors in both the CT2015 and
observations 1000 times. (See  Sect. S4 and Fig. S9 for
details on parameterizing CT2015 uncertainty.) The relevant quantiles
are obtained from the resulting distribution, and are reported
relative to the mean <inline-formula><mml:math id="M162" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> of the original data
subset. We follow a slightly modified approach for <inline-formula><mml:math id="M163" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">mod</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> in that we construct monthly and seasonal
residual pools from daily averages of hourly afternoon
<inline-formula><mml:math id="M164" display="inline"><mml:mrow><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">mod</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>-</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula>. The residuals – the
deviation of the model from the true observed values – represent the
total uncertainty in the model and therefore aggregate the effects of
uncertainty in the footprints, background, and inventories. Monthly
and seasonal 95 % confidence intervals of
<inline-formula><mml:math id="M165" display="inline"><mml:mrow><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">mod</mml:mi></mml:mrow></mml:msub></mml:mrow><mml:mo>-</mml:mo><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> are then obtained from the
distribution of bootstrapping the residual pools 1000 times. We then
obtain the mean and 95 % confidence interval of <inline-formula><mml:math id="M166" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">mod</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> by applying the relevant quantiles of the
residuals to the mean <inline-formula><mml:math id="M167" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">obs</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> of the original
data subset. Similar to Sargent et al. (2018) and McKain
et al. (2015), distributions of seasonal averages obtained from the
above method are used to estimate annual averages and 95 %
confidence intervals.</p>
      <p id="d1e2551">Sargent et al. (2018) note that applying the same meteorological model
over a long time period (15 months) allows for detection of trends in
transport uncertainty. In this study, the drawback of a single
location is offset somewhat by a much longer time series
(60 months). Absent a dense network of observations, a more
sophisticated and extensive error analysis cannot be conducted with
meaningful results. Turnbull et al. (2011) faced a similar issue,
where weekly flask data collected between 2004 and 2010 from two sites
in the NOAA ESRL/WMO sampling network were used to evaluate
a bottom-up fossil inventory based on CDIAC and EDGAR
estimates. Turnbull et al. (2011) noted the difficulty in assessing
the transport error given the paucity of regional observations but
also demonstrate the power of top-down assessments given improvements
in regional transport modeling and density of observations.</p><?xmltex \hack{\newpage}?>
</sec>
</sec>
</sec>
<?pagebreak page3577?><sec id="Ch1.S4">
  <label>4</label><title>Results and discussion</title>
<sec id="Ch1.S4.SS1">
  <label>4.1</label><title>Impact of seasonality on evaluation region</title>
      <p id="d1e2573">As shown in Fig. 2, we find strong seasonality in the footprint
percentile contours, in agreement with previous analysis of Miyun
observations by Wang et al. (2010). At annual timescales, the
L_0.90 region is comparable to the WRF d02 extent. Northern China,
including Inner Mongolia, dominates the L_0.90 region both
seasonally and annually. Due to the heavy biosphere influence in the
regional growing season, previous work by Wang et al. (2010) used
Miyun non-growing-season measurements of <inline-formula><mml:math id="M168" 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 carbon
monoxide (CO) as an anthropogenic tracer to estimate combustion
efficiency for China. When compared to bottom-up estimates of national
combustion efficiency, observations suggested 25 % higher
combustion efficiency than bottom-up estimates of national combustion
efficiency; however, Wang et al. (2010) note that the regional
(northern China) and seasonal (winter) subsets could contribute to
such a discrepancy.  The seasonality exhibited in Fig. 2 indeed
suggests that combustion efficiency estimates derived from non-growing-season measurements alone do not represent anthropogenic processes in
provinces south of Miyun that are visible in the observations
primarily during the growing season. Low-emitting regions northwest of
Miyun such as Inner Mongolia influence the site more in the fall and
winter relative to other seasons. In the spring and summer, higher-emitting regions in provinces south of Miyun are more
influential. However, non-growing-season <inline-formula><mml:math id="M169" 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> is influenced
by often inefficient district heating in the northwest. And, while
growing-season <inline-formula><mml:math id="M170" 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> is influenced by intense urban activities
from Beijing and other cities to the south, vegetation draws down both
background and locally observed <inline-formula><mml:math id="M171" 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> significantly (Fig. 3a).</p>
</sec>
<sec id="Ch1.S4.SS2">
  <label>4.2</label><title>Unscaled models: performance at multiple timescales</title>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T1" specific-use="star"><?xmltex \currentcnt{1}?><label>Table 1</label><caption><p id="d1e2631">Quantification of model–observation mismatch at hourly
timescales averaged over 2005–2009 and pooled by season (W <inline-formula><mml:math id="M172" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> winter;
Sp <inline-formula><mml:math id="M173" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> spring; Su <inline-formula><mml:math id="M174" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> summer; F <inline-formula><mml:math id="M175" display="inline"><mml:mo>=</mml:mo></mml:math></inline-formula> fall). We provide standard major
axis (SMA) slopes and 95 % confidence intervals, <inline-formula><mml:math id="M176" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula>
quantities (those <inline-formula><mml:math id="M177" display="inline"><mml:mo>&gt;</mml:mo></mml:math></inline-formula> 0.2 are in bold), and mean bias and root mean
square error (RMSE) in ppm.</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="7">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="left"/>
     <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:thead>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col7">SMA slope (95 % CI) </oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3">All</oasis:entry>
         <oasis:entry colname="col4">W (JFM)</oasis:entry>
         <oasis:entry colname="col5">Sp (AMJ)</oasis:entry>
         <oasis:entry colname="col6">Su (JAS)</oasis:entry>
         <oasis:entry colname="col7">F (OND)</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M178" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3">0.89 (0.88,0.91)</oasis:entry>
         <oasis:entry colname="col4">1.0 (1.0,1.1)</oasis:entry>
         <oasis:entry colname="col5">0.74 (0.72,0.77)</oasis:entry>
         <oasis:entry colname="col6">0.88 (0.84,0.92)</oasis:entry>
         <oasis:entry colname="col7">0.92 (0.90,0.95)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M179" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3">0.77 (0.76, 0.78)</oasis:entry>
         <oasis:entry colname="col4">0.83 (0.81, 0.86)</oasis:entry>
         <oasis:entry colname="col5">0.62 (0.60, 0.65)</oasis:entry>
         <oasis:entry colname="col6">0.83 (0.80, 0.87)</oasis:entry>
         <oasis:entry colname="col7">0.77 (0.74, 0.79)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M180" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3">0.63 (0.62, 0.64)</oasis:entry>
         <oasis:entry colname="col4">0.63 (0.62, 0.65)</oasis:entry>
         <oasis:entry colname="col5">0.48 (0.46, 0.50)</oasis:entry>
         <oasis:entry colname="col6">0.79 (0.75, 0.82)</oasis:entry>
         <oasis:entry colname="col7">0.56 (0.54, 0.58)</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col7"><inline-formula><mml:math id="M181" display="inline"><mml:mrow><mml:msup><mml:mi>R</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msup></mml:mrow></mml:math></inline-formula></oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3">All</oasis:entry>
         <oasis:entry colname="col4">W (JFM)</oasis:entry>
         <oasis:entry colname="col5">Sp (AMJ)</oasis:entry>
         <oasis:entry colname="col6">Su (JAS)</oasis:entry>
         <oasis:entry colname="col7">F (OND)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M182" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3"><bold>0.49</bold></oasis:entry>
         <oasis:entry colname="col4"><bold>0.56</bold></oasis:entry>
         <oasis:entry colname="col5"><bold>0.26</bold></oasis:entry>
         <oasis:entry colname="col6"><bold>0.22</bold></oasis:entry>
         <oasis:entry colname="col7"><bold>0.56</bold></oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M183" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3"><bold>0.47</bold></oasis:entry>
         <oasis:entry colname="col4"><bold>0.55</bold></oasis:entry>
         <oasis:entry colname="col5"><bold>0.21</bold></oasis:entry>
         <oasis:entry colname="col6">0.18</oasis:entry>
         <oasis:entry colname="col7"><bold>0.55</bold></oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M184" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3"><bold>0.43</bold></oasis:entry>
         <oasis:entry colname="col4"><bold>0.55</bold></oasis:entry>
         <oasis:entry colname="col5">0.17</oasis:entry>
         <oasis:entry colname="col6">0.13</oasis:entry>
         <oasis:entry colname="col7"><bold>0.54</bold></oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry namest="col1" nameend="col7">Mean bias (RMSE), ppm </oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3">All</oasis:entry>
         <oasis:entry colname="col4">W (JFM)</oasis:entry>
         <oasis:entry colname="col5">Sp (AMJ)</oasis:entry>
         <oasis:entry colname="col6">Su (JAS)</oasis:entry>
         <oasis:entry colname="col7">F (OND)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M185" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3">0.32 (9.2)</oasis:entry>
         <oasis:entry colname="col4">0.014 (7.9)</oasis:entry>
         <oasis:entry colname="col5"><inline-formula><mml:math id="M186" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">0.033</mml:mn></mml:mrow></mml:math></inline-formula> (8.3)</oasis:entry>
         <oasis:entry colname="col6">3.1 (11)</oasis:entry>
         <oasis:entry colname="col7"><inline-formula><mml:math id="M187" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1.1</mml:mn></mml:mrow></mml:math></inline-formula> (9.7)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M188" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3"><inline-formula><mml:math id="M189" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>2.0 (9.3)</oasis:entry>
         <oasis:entry colname="col4"><inline-formula><mml:math id="M190" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>2.2 (7.7)</oasis:entry>
         <oasis:entry colname="col5"><inline-formula><mml:math id="M191" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.9 (8.7)</oasis:entry>
         <oasis:entry colname="col6">0.25 (10.8)</oasis:entry>
         <oasis:entry colname="col7"><inline-formula><mml:math id="M192" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>3.4 (10.1)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry namest="col1" nameend="col2"><inline-formula><mml:math id="M193" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula></oasis:entry>
         <oasis:entry colname="col3"><inline-formula><mml:math id="M194" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>3.3 (9.9)</oasis:entry>
         <oasis:entry colname="col4"><inline-formula><mml:math id="M195" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>3.1 (8.1)</oasis:entry>
         <oasis:entry colname="col5"><inline-formula><mml:math id="M196" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>3.3 (9.2)</oasis:entry>
         <oasis:entry colname="col6"><inline-formula><mml:math id="M197" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.1 (11.3)</oasis:entry>
         <oasis:entry colname="col7"><inline-formula><mml:math id="M198" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>5.0 (11.1)</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

      <p id="d1e3276">We evaluate unscaled model performance relative to observations at
hourly, seasonal, and annual timescales. While inventory scaling is
performed at the policy-relevant scales of seasons and years,
examination of the models at shorter<?pagebreak page3578?> timescales provides insight into
model bias and error aggregation at longer timescales. Table 1
summarizes hourly model bias across all years and pooled by season.</p>
      <p id="d1e3279">All modeled hourly quantities include the same biological component
from VPRM, background concentrations, and transport models such that
the only source of variation among models is the anthropogenic
inventory. With a few exceptions that are discussed in the following
sections, <inline-formula><mml:math id="M199" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M200" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula>, <inline-formula><mml:math id="M201" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula>, and <inline-formula><mml:math id="M202" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> systematically
underestimate observations, as indicated by larger deviation below the
<inline-formula><mml:math id="M203" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mo>:</mml:mo><mml:mn mathvariant="normal">1</mml:mn></mml:mrow></mml:math></inline-formula> line in the comparison of modeled to measured <inline-formula><mml:math id="M204" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><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:mrow></mml:math></inline-formula> (Table 1, Fig. 3b–d.)</p>
<sec id="Ch1.S4.SS2.SSS1">
  <label>4.2.1</label><title>Hourly</title>
      <p id="d1e3403">We examine the distribution of modeled-measured residuals at hourly
timescales for each anthropogenic inventory. While standard deviations
are consistent across all models of <inline-formula><mml:math id="M205" 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> flux (<inline-formula><mml:math id="M206" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mi mathvariant="italic">σ</mml:mi><mml:mo>=</mml:mo><mml:mn mathvariant="normal">9</mml:mn></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M207" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>; Fig. 3e–g) <inline-formula><mml:math id="M208" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> exhibits the
least bias relative to observations with a mean residual of
<inline-formula><mml:math id="M209" display="inline"><mml:mrow><mml:mn mathvariant="normal">0.32</mml:mn><mml:mo>(</mml:mo><mml:mn mathvariant="normal">0.12</mml:mn><mml:mo>,</mml:mo><mml:mn mathvariant="normal">0.53</mml:mn><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M210" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>. In contrast, <inline-formula><mml:math id="M211" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula>
and <inline-formula><mml:math id="M212" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> display significantly greater bias by
typically underestimating observations by large amounts: <inline-formula><mml:math id="M213" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2.0</mml:mn><mml:mo>(</mml:mo><mml:mo>-</mml:mo><mml:mn mathvariant="normal">1.8</mml:mn><mml:mo>,</mml:mo><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2.2</mml:mn><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M214" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula> and <inline-formula><mml:math id="M215" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3.3</mml:mn><mml:mo>(</mml:mo><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3.1</mml:mn><mml:mo>,</mml:mo><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3.5</mml:mn><mml:mo>)</mml:mo></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M216" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>, respectively.
Here, the 95 % confidence intervals are derived from a two-sample
<inline-formula><mml:math id="M217" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> test.  The EDGAR and CDIAC underestimation of <inline-formula><mml:math id="M218" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M219" 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> at the hourly scale is consistent across longer
timescales of seasons and years, as discussed in the following
sections, but we note where there are likely aliased effects of the
uncertainty in the VPRM biogenic component.</p><?xmltex \hack{\newpage}?>
</sec>
<sec id="Ch1.S4.SS2.SSS2">
  <label>4.2.2</label><title>Seasonal</title>
      <p id="d1e3633">The seasonally averaged modeled and measured <inline-formula><mml:math id="M220" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M221" 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>
values shown in Fig. 4 illustrate the overall biases for the four
inventories. Outside of June, July, August, and September, the
anthropogenic signal dominates in northern China (Wang et al.,
2010). We see from Table 1 that during seasons where biological
activity is lower or significantly lower than anthropogenic activity,
there is a consistent discrepancy among the <inline-formula><mml:math id="M222" 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> modeled by
the three different anthropogenic inventories suggesting systematic
differences largely attributable to the anthropogenic component (as we
do not vary any other component).  In the fall, where respiration is
the dominant biological process, all three modeled quantities are
consistently lower than observations – a likely a consequence of the
known underestimate of ecosystem respiration by the VPRM (Dayalu
et al., 2018a). Even so, China's significant anthropogenic component
still dominates during these months.  During the winter season, where
all biospheric activity is at a minimum, the model–observation
mismatch is most reflective of biases among anthropogenic inventories
rather than aliased impacts from the VPRM. As shown in the winter data
in Table 1, ZHAO displays the least bias relative to observations
(0.01 <inline-formula><mml:math id="M223" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>), followed by EDGAR (<inline-formula><mml:math id="M224" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2.2</mml:mn></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M225" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>) and CDIAC
(<inline-formula><mml:math id="M226" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">3.1</mml:mn></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M227" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F4" specific-use="star"><?xmltex \currentcnt{4}?><label>Figure 4</label><caption><p id="d1e3711">Modeled and measured seasonal <inline-formula><mml:math id="M228" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M229" 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>. CT2015 background is subtracted from observations to provide observed <inline-formula><mml:math id="M230" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M231" 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> (black line), and 95 % confidence bounds are derived from bootstrapping hourly afternoon concentrations for each season.</p></caption>
            <?xmltex \igopts{width=412.564961pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f04.png"/>

          </fig>

      <p id="d1e3754">With the exception of the peak JAS growing season, <inline-formula><mml:math id="M232" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> and <inline-formula><mml:math id="M233" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> typically
underestimate <inline-formula><mml:math id="M234" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula>CO<inline-formula><mml:math id="M235" display="inline"><mml:msub><mml:mi/><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mtext>OBS</mml:mtext></mml:mrow></mml:msub></mml:math></inline-formula>, even within the 95 %
uncertainty bounds. The VPRM has a limited calibration network that
contributes to an underestimate of regional <inline-formula><mml:math id="M236" 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> drawdown
during the growing season (Dayalu et al., 2018a). Therefore, while
<inline-formula><mml:math id="M237" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> agrees within 95 % confidence bounds
with <inline-formula><mml:math id="M238" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">OBS</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> during the non-growing seasons,
<inline-formula><mml:math id="M239" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> generally overestimates <inline-formula><mml:math id="M240" 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>
concentrations in the growing season (Fig. 4a). <inline-formula><mml:math id="M241" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">EDGAR</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> (Fig. 4b) and <inline-formula><mml:math id="M242" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> (Fig. 4c) display lower <inline-formula><mml:math id="M243" 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> concentrations and generally
result in better agreement<?pagebreak page3579?> with observations during the peak growing
season than at other times of the year; however, our wintertime and
overall analysis at hourly timescales (Fig. 4, Table 1) suggests this
is an artifact of lower anthropogenic emissions estimates relative to
ZHAO that counteracts the VPRM underestimating drawdown. Even during
the growing season, <inline-formula><mml:math id="M244" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">CDIAC</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> agrees with
observations typically at its upper confidence limits. However, during
times of the year where the impacts of underestimated respiration
become more significant (e.g., Fall) it is possible that the seemingly
better agreement of ZHAO <inline-formula><mml:math id="M245" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM is linked to a counteracting effect of
overestimated anthropogenic emissions.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F5"><?xmltex \currentcnt{5}?><label>Figure 5</label><caption><p id="d1e4003">Modeled mean monthly contribution (ppm) to Miyun CO2 concentrations from vegetation (VPRM) and anthropogenic (ZHAO) sources. Enhancement and depletion are relative to advected CT2015 background concentrations during the regional growing season (MJJAS), averaged over 2005 to 2009. Vertical lines represent <inline-formula><mml:math id="M246" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mi mathvariant="italic">σ</mml:mi></mml:mrow></mml:math></inline-formula> of monthly averages (green: vegetation; black: anthropogenic). Negative values represent depletion from CT2015 background; positive values represent enhancement of CT2015 background.</p></caption>
            <?xmltex \igopts{width=227.622047pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f05.png"/>

          </fig>

      <p id="d1e4022">As ZHAO <inline-formula><mml:math id="M247" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM demonstrates the least bias relative to observations at
hourly and seasonal scales, we model the relative contributions to the
monthly signal during the May through September peak regional growing
season as defined by Wang et al. (2010). Figure 5 displays the results
from partitioning the mean monthly  <inline-formula><mml:math id="M248" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula>
signal as a multi-year average into anthropogenic and vegetation
contributions. While the WRF-STILT-VPRM framework has been
successfully adapted for similar <inline-formula><mml:math id="M249" 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> inventory evaluation
studies in North American regions where biogenic fluxes dominate
surface processes (Karion et al., 2016; Matross et al., 2006), Fig. 5
shows the relative magnitude of biogenic fluxes and anthropogenic
emissions in the northern China region is comparable during peak
summer, making it difficult to independently constrain them with
observational data. As noted in Sect. 3, the regional peak uptake
during the growing season occurs with the onset of the corn growing
season around July and August. The atypical lower uptake during June
represents the winter wheat to corn transition period. These results are
consistent with the biological component estimated by Turnbull
et al. (2011). Furthermore, knowledge of the relative contribution of
vegetation and anthropogenic processes to the <inline-formula><mml:math id="M250" 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> signal
during the peak growing season is necessary to interpret satellite
retrievals of <inline-formula><mml:math id="M251" 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> over the region (Dayalu et al., 2018a).</p>
</sec>
<?pagebreak page3580?><sec id="Ch1.S4.SS2.SSS3">
  <label>4.2.3</label><title>Annual</title>
      <p id="d1e4096">Aggregation of uncertainty and anthropogenic inventory biases at
shorter timescales becomes most apparent at the annual timescales. For
annual budgeting we follow the assumptions of Piao et al. (2009) and
Jiang et al. (2016) that agricultural systems are in annual carbon
balance because crop biomass has a short residence time. In the
absence of data on regional transfer of agricultural products and
proportion of grains used in situ for livestock vs. human consumption
in China this is the most conservative assumption to make. Given the
dense population in most of Beijing province we expect there may be
net import of agricultural products from outside the L_0.90 region,
which would show up as additional respiration not captured by VPRM,
but that term will be small relative to the anthropogenic
<inline-formula><mml:math id="M252" 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> (Fig. 5) (Dayalu et al., 2018a).  Therefore, while the
VPRM is implicitly included in the modeled annual <inline-formula><mml:math id="M253" 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="M254" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M255" 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>, vegetation carbon stocks (including harvested
products and crop residues) from the portions of the L_0.90 region with
widespread agriculture largely turn over such that only the
anthropogenic inventories dominate the modeled <inline-formula><mml:math id="M256" 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>
signal. We evaluate annual <inline-formula><mml:math id="M257" 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> including CT2015 background
(Fig. 6a–c) and as regional enhancement relative to background
(Fig. 6d–f). We show that for all years, <inline-formula><mml:math id="M258" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:math></inline-formula> and
<inline-formula><mml:math id="M259" display="inline"><mml:mrow><mml:mi mathvariant="normal">Δ</mml:mi><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mi mathvariant="normal">ZHAO</mml:mi><mml:mo>+</mml:mo><mml:mi mathvariant="normal">VPRM</mml:mi></mml:mrow></mml:msub></mml:mrow></mml:mrow></mml:math></inline-formula> agree tightly within 95 % uncertainty
to observations (Fig. 6a and d).  EDGAR <inline-formula><mml:math id="M260" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM and CDIAC <inline-formula><mml:math id="M261" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM are
consistently biased significantly lower than observations.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F6" specific-use="star"><?xmltex \currentcnt{6}?><label>Figure 6</label><caption><p id="d1e4220">Mean annual <inline-formula><mml:math id="M262" 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="M263" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M264" 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> over the entire study time period. <bold>(a–c)</bold> <inline-formula><mml:math id="M265" 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> annual concentration; <bold>(d–f)</bold> <inline-formula><mml:math id="M266" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M267" 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> (regional enhancement, after removal of advected CT2015 background) with bootstrapped 95 % confidence intervals.</p></caption>
            <?xmltex \igopts{width=426.791339pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f06.png"/>

          </fig>

</sec>
</sec>
<sec id="Ch1.S4.SS3">
  <label>4.3</label><title>Evaluation of inventories at seasonal and annual timescales</title>
      <p id="d1e4301">We quantify model–observation mismatch by estimating the additive flux
corrections at seasonal timescales and multiplicative corrections at
annual timescales. We emphasize that these “corrections”, or
scalings, are not optimizations; rather, they simply reflect the
extent to which the individual anthropogenic <inline-formula><mml:math id="M268" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM flux models
deviate from the observations.  Complete seasonal and annual scaling
results are provided in Sect. S5 and Tables S2–S3.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F7" specific-use="star"><?xmltex \currentcnt{7}?><label>Figure 7</label><caption><p id="d1e4313">Scaled seasonal fluxes in the L_0.90 region (<inline-formula><mml:math id="M269" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msub><mml:mi mathvariant="normal">CO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub><mml:mspace width="0.125em" linebreak="nobreak"/><mml:msup><mml:mi mathvariant="normal">m</mml:mi><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">2</mml:mn></mml:mrow></mml:msup></mml:mrow></mml:math></inline-formula> per month). Anthropogenic and vegetation inventories are scaled together ([ANTH<inline-formula><mml:math id="M270" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula>VPRM_COR]). The black and yellow dashed line is the seasonal flux estimated by the original ANTH<inline-formula><mml:math id="M271" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula>VPRM model. All models have the same vegetation component (VPRM) and differ only in the anthropogenic inventory source. Shaded green represents negative flux (uptake by biosphere). The scaling based on additive corrections; the difference among scaled inventories is due to differing spatial allocations by anthropogenic inventories. Bootstrapped 95 % confidence intervals are represented by the black vertical lines.</p></caption>
          <?xmltex \igopts{width=312.980315pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f07.png"/>

        </fig>

      <p id="d1e4359">The observational record informing the scaling integrates the
biological and anthropogenic signals. At the seasonal scale, where
biological processes are significant contributors to the signal, we
scale the sum of the anthropogenic and biological fluxes
(Fig. 7). Scaled non-growing-season flux estimates are higher than
unscaled values, partially accounting for the VPRM generally
underestimating ecosystem respiration by an additive offset throughout
the year (Dayalu et al., 2018a). The multi-year seasonal results in
Table 1 suggest that this offset can aggregate to a 1–2 <inline-formula><mml:math id="M272" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula>
difference; the result would be a shift in baseline rather than
overall pattern for each of the three simulations. As the vegetation
and all other components are controlled across models, the inter-model
variance reflects the relative performance of the anthropogenic
estimates. We find that in the non-growing months the original
ZHAO <inline-formula><mml:math id="M273" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM inventory typically remains within the 95 % confidence
bounds of the scaled inventory. However, both EDGAR <inline-formula><mml:math id="M274" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM and
CDIAC <inline-formula><mml:math id="M275" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM are consistently significantly lower than their scaled
counterparts. At least in the winter, where biogenic processes are at
a minimum, this suggests that both EDGAR and CDIAC underestimate
anthropogenic emissions, and that ZHAO estimates are closer to actual
emissions. Improved representation of temporal anthropogenic activity
factors and biosphere processes are needed to extend the conclusions
of anthropogenic inventory performance to all seasons. In the absence
of such data, it is not possible to conclusively state whether
model–data mismatch is rooted in anthropogenic emissions biases or
biogenic biases. During the growing seasons, however, the afternoon
vegetation signal is significant, and the picture is more complex. In
the spring, the <inline-formula><mml:math id="M276" 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> signal at Miyun is significantly
affected by the North China Plain winter wheat growing season. The
effect of scaling in the spring from 2005 to 2007 is to increase
<inline-formula><mml:math id="M277" 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> emissions with a net positive seasonal flux; however, in
2008 and 2009 we find the net seasonal flux becomes negative such that
uptake dominates emissions. The prior models in all cases predict
positive flux. During the summer months, ZHAO <inline-formula><mml:math id="M278" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM predicts more
emissions and/or less uptake relative to EDGAR <inline-formula><mml:math id="M279" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM and
CDIAC <inline-formula><mml:math id="M280" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM. Scaling of summertime fluxes serves to significantly
increase ZHAO <inline-formula><mml:math id="M281" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM uptake estimates; the EDGAR <inline-formula><mml:math id="M282" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM and
CDIAC <inline-formula><mml:math id="M283" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM prior estimates are within the 95 % confidence bounds
of the scaling for reasons discussed previously.</p>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T2"><?xmltex \currentcnt{2}?><label>Table 2</label><caption><p id="d1e4461">Annual scaling factors (95 % CI) and corresponding corrected
emissions for the L_0.90 inventory evaluation region.</p></caption><oasis:table frame="topbot"><?xmltex \begin{scaleboxenv}{.85}[.85]?><oasis:tgroup cols="5">
     <oasis:colspec colnum="1" colname="col1" align="left"/>
     <oasis:colspec colnum="2" colname="col2" align="left"/>
     <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:thead>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3">Scaling factor</oasis:entry>
         <oasis:entry colname="col4">Corrected emissions,</oasis:entry>
         <oasis:entry colname="col5">Original</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3">(95 % CI)</oasis:entry>
         <oasis:entry colname="col4">MtCO<inline-formula><mml:math id="M284" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula> (95 % CI)</oasis:entry>
         <oasis:entry colname="col5">emissions,</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2"/>
         <oasis:entry colname="col3"/>
         <oasis:entry colname="col4"/>
         <oasis:entry colname="col5">MtCO<inline-formula><mml:math id="M285" display="inline"><mml:msub><mml:mi/><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:math></inline-formula></oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry colname="col1">2005</oasis:entry>
         <oasis:entry colname="col2">ZHAO</oasis:entry>
         <oasis:entry colname="col3">0.95 (0.84, 1.0)</oasis:entry>
         <oasis:entry colname="col4">2800 (2476, 3105)</oasis:entry>
         <oasis:entry colname="col5">3015</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">EDGAR</oasis:entry>
         <oasis:entry colname="col3">1.4 (1.3, 1.6)</oasis:entry>
         <oasis:entry colname="col4">3306 (2886, 3683)</oasis:entry>
         <oasis:entry colname="col5">2322</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">CDIAC</oasis:entry>
         <oasis:entry colname="col3">1.7 (1.5, 1.9)</oasis:entry>
         <oasis:entry colname="col4">3489 (3017, 3871)</oasis:entry>
         <oasis:entry colname="col5">1930</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2006</oasis:entry>
         <oasis:entry colname="col2">ZHAO</oasis:entry>
         <oasis:entry colname="col3">1.0 (0.91, 1.1)</oasis:entry>
         <oasis:entry colname="col4">3326 (2972, 3631)</oasis:entry>
         <oasis:entry colname="col5">3273</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">EDGAR</oasis:entry>
         <oasis:entry colname="col3">1.5 (1.3, 1.6)</oasis:entry>
         <oasis:entry colname="col4">3751 (3325, 4150)</oasis:entry>
         <oasis:entry colname="col5">2586</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">CDIAC</oasis:entry>
         <oasis:entry colname="col3">1.9 (1.6, 2.0)</oasis:entry>
         <oasis:entry colname="col4">3930 (3438, 4338)</oasis:entry>
         <oasis:entry colname="col5">2160</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2007</oasis:entry>
         <oasis:entry colname="col2">ZHAO</oasis:entry>
         <oasis:entry colname="col3">0.94 (0.85, 1.0)</oasis:entry>
         <oasis:entry colname="col4">3080 (2789, 3324)</oasis:entry>
         <oasis:entry colname="col5">3588</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">EDGAR</oasis:entry>
         <oasis:entry colname="col3">1.4 (1.2, 1.5)</oasis:entry>
         <oasis:entry colname="col4">3454 (3096, 3785)</oasis:entry>
         <oasis:entry colname="col5">2799</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">CDIAC</oasis:entry>
         <oasis:entry colname="col3">1.6 (1.5, 1.8)</oasis:entry>
         <oasis:entry colname="col4">3180 (2842, 3493)</oasis:entry>
         <oasis:entry colname="col5">2260</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2008</oasis:entry>
         <oasis:entry colname="col2">ZHAO</oasis:entry>
         <oasis:entry colname="col3">0.94 (0.82, 1.0)</oasis:entry>
         <oasis:entry colname="col4">3422 (3008, 3768)</oasis:entry>
         <oasis:entry colname="col5">3685</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">EDGAR</oasis:entry>
         <oasis:entry colname="col3">1.2 (1.1, 1.4)</oasis:entry>
         <oasis:entry colname="col4">3790 (3332, 4207)</oasis:entry>
         <oasis:entry colname="col5">3095</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">CDIAC</oasis:entry>
         <oasis:entry colname="col3">1.7 (1.5, 1.9)</oasis:entry>
         <oasis:entry colname="col4">3941 (3461, 4374)</oasis:entry>
         <oasis:entry colname="col5">2395</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2009</oasis:entry>
         <oasis:entry colname="col2">ZHAO</oasis:entry>
         <oasis:entry colname="col3">0.96 (0.86, 1.1)</oasis:entry>
         <oasis:entry colname="col4">3860 (3474, 4251)</oasis:entry>
         <oasis:entry colname="col5">3974</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">EDGAR</oasis:entry>
         <oasis:entry colname="col3">1.1 (1.0, 1.3)</oasis:entry>
         <oasis:entry colname="col4">3518 (3133, 3874)</oasis:entry>
         <oasis:entry colname="col5">3298</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">CDIAC</oasis:entry>
         <oasis:entry colname="col3">1.5 (1.3, 1.7)</oasis:entry>
         <oasis:entry colname="col4">3921 (3454, 4330)</oasis:entry>
         <oasis:entry colname="col5">2543</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup><?xmltex \end{scaleboxenv}?></oasis:table></table-wrap>

      <?pagebreak page3581?><p id="d1e4811">We report annual scaled anthropogenic inventories in the L_0.90
region in Fig. 8 and Table 2 as <inline-formula><mml:math id="M286" display="inline"><mml:mrow class="chem"><mml:msub><mml:mi mathvariant="normal">MtCO</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M287" display="inline"><mml:mrow class="unit"><mml:msup><mml:mi mathvariant="normal">yr</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>. As
discussed previously, the annual scalings are applied only to the
anthropogenic inventory, as the signal at the annual timescale is
effectively dominated by anthropogenic emissions; net ecosystem fluxes
are expected to be relatively minor in the L_0.90 region in
comparison. For all years, the emissions estimated by the original
ZHAO inventory lie within the 95 % confidence bounds of the scaled
ZHAO inventory. However, for EDGAR and CDIAC, the original inventories
consistently underestimate observations.  Averaged over the 5-year
study period, EDGAR and CDIAC lead to modeled estimates of
<inline-formula><mml:math id="M288" 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> mixing ratios that are typically lower than observations
by 30 % and 70 % respectively (Fig. 6). Averaged across the
5 years, this translates to EDGAR and CDIAC being scaled relative
to their unscaled values in the L_0.90 region by 1.3 and 1.7,
respectively (Fig. 8; Table 2). In the case of EDGAR, we note
a general increase in observational agreement from 2005 to 2009.</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F8"><?xmltex \currentcnt{8}?><label>Figure 8</label><caption><p id="d1e4852">Annually scaled emissions in the L_0.90 region. Scaling is based on
multiplicative scaling factors. Difference among scaled inventory means is due
to differing spatial allocations in original anthropogenic
inventories. Bootstrapped 95 % confidence intervals are represented by the
black vertical lines. <inline-formula><mml:math id="M289" display="inline"><mml:msup><mml:mi/><mml:mo>*</mml:mo></mml:msup></mml:math></inline-formula> Note the <inline-formula><mml:math id="M290" display="inline"><mml:mi>y</mml:mi></mml:math></inline-formula> axis origin begins at 1000 Mt <inline-formula><mml:math id="M291" 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> for visual clarity.</p></caption>
          <?xmltex \igopts{width=241.848425pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f08.png"/>

        </fig>

</sec>
<sec id="Ch1.S4.SS4">
  <label>4.4</label><title>Potential contributions to regional carbon emissions patterns from 2005
to 2009</title>
      <p id="d1e4896">We examine the statistical significance of the inter-annual observed
concentration and enhancement differences using a two-sample <inline-formula><mml:math id="M292" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> test
(Table 3). The observed concentrations including advected global
background (Fig. 6a–c) display an overall increasing trend of 1.87
(1.8, 1.9) <inline-formula><mml:math id="M293" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">ppm</mml:mi></mml:mrow></mml:math></inline-formula> <inline-formula><mml:math id="M294" 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="M295" display="inline"><mml:mrow class="unit"><mml:msup><mml:mi mathvariant="normal">yr</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> between 2005 and
2009, in agreement with flask samples obtained from nearby WMO sites
between 2007 and 2010 (Liu et al., 2015). The inter-annual increases
are statistically significant (Table 3). However, when we remove the
modeled background to more closely examine regional patterns that
would otherwise be drowned out by the global signal, we find that the
regional <inline-formula><mml:math id="M296" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M297" 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> trend (Fig. 6d–f; Table 3) does not
parallel the increasing global <inline-formula><mml:math id="M298" 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> trend (Fig. 6a–c;
Table 3). Regionally, the observed enhancements increase from 2005 to
2006 and plateau in 2007 before decreasing in 2008. Regional <inline-formula><mml:math id="M299" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M300" 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> increases again in 2009. Earlier work by Wang
et al. (2010) extended the Miyun observations of <inline-formula><mml:math id="M301" 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> growth
rate to all of China and estimates a lower <inline-formula><mml:math id="M302" 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> growth rate
than previously suggested. However, Fig. S6 suggests local reductions
in regions influencing Miyun, possibly in preparation for the Beijing
Olympics, are partially offset by increases elsewhere. A larger
network of sites would be needed to quantify this further in order to
evaluate the <inline-formula><mml:math id="M303" 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> growth rate for other regions in China and
for China as a whole.</p>
      <p id="d1e5018">In Fig. 9a we estimate gross regional product (GRP) for 8 of
China's 34 provincial-level administrative units, specifically those
encompassed significantly by the L_0.90 region: Beijing, Tianjin,
Henan, Shanxi, Shandong, Hebei, Inner Mongolia, and Liaoning. Using
data from the International Monetary Fund (IMF;
<uri>https://www.imf.org/en/Data</uri>, last access: 9 February 2020) and World Bank (World Bank, 2017)
we retrieved the GDP for each of the above provinces and summed them
to estimate the GRP. GDP calculations are inherently uncertain and
were available as single values for each province per year. A more
extensive economic analysis to estimate the uncertainty of these values is
beyond the scope of this study. Key economic events occurred during
the study time period and are likely contributors to the observed
interannual variation in regional <inline-formula><mml:math id="M304" 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> emissions (Fig. 6d–e)
and a doubling of GRP from 2005 to 2009 (Fig. 9a). In particular, the
time period from 2005 to 2009 saw industrial energy efficiency
improvements which began in 2007 under the 11th FYP, preparations for
and staging of the 2008 Beijing Summer Olympics, the global financial
crisis in late 2008, and a large Chinese fiscal stimulus in 2009. We
further note that the global financial crisis of 2008 correlates with
a<?pagebreak page3582?> plateauing of the percentage contribution of northern China GRP to
national GDP (Fig. 9a).</p>

      <?xmltex \floatpos{t}?><fig id="Ch1.F9" specific-use="star"><?xmltex \currentcnt{9}?><label>Figure 9</label><caption><p id="d1e5037">Estimates of regional carbon intensity
(<inline-formula><mml:math id="M305" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi></mml:mrow></mml:math></inline-formula> of <inline-formula><mml:math id="M306" 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> per USD). <bold>(a)</bold> PPP GRP by year and as a percentage of China's national GDP. No PPP GRP values were available for 2006 and
2007; PPP GRP for these years was derived from a linearly interpolated ratio of
nominal GRP/PPP GRP for 2005, 2008, and 2009. <bold>(b)</bold> Correlating
corrected regional emissions from Table 2 with PPP GRP; values are pooled
annual means among ZHAO, EDGAR, and CDIAC with <inline-formula><mml:math id="M307" display="inline"><mml:mrow><mml:mn mathvariant="normal">1</mml:mn><mml:mi mathvariant="italic">σ</mml:mi></mml:mrow></mml:math></inline-formula> error
bars. <bold>(c)</bold> Regional carbon intensity using scaled (solid) and unscaled
(grey) <inline-formula><mml:math id="M308" 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> estimates. Error bars are bootstrapped 95 % confidence
intervals. GRP and GDP data are from the IMF and World Bank. Provinces used in GRP
calculation are those significantly encompassed by the L_0.90 region: Beijing,
Henan, Shanxi, Tianjin, Shandong, Hebei, Inner Mongolia, and
Liaoning. <inline-formula><mml:math id="M309" display="inline"><mml:msup><mml:mi/><mml:mo>*</mml:mo></mml:msup></mml:math></inline-formula> Estimated by scaling the official national emissions total by the average contribution (39 %) of the L_0.90 region to total emissions in 2005. Uncertainty bars represent the percentage contribution range estimated by ZHAO, EDGAR, and CDIAC in 2005 (35 %, 42 %).</p></caption>
          <?xmltex \igopts{width=341.433071pt}?><graphic xlink:href="https://acp.copernicus.org/articles/20/3569/2020/acp-20-3569-2020-f09.png"/>

        </fig>

<?xmltex \floatpos{t}?><table-wrap id="Ch1.T3"><?xmltex \currentcnt{3}?><label>Table 3</label><caption><p id="d1e5109">Inter-annual observed <inline-formula><mml:math id="M310" 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="M311" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M312" 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> differences.  Differences are of observations between
consecutive years. The 95 % confidence intervals are derived from
a two-sample <inline-formula><mml:math id="M313" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> test. Italicized entries denote instances where the
inter-annual difference is not statistically significant (confidence
interval includes zero).</p></caption><oasis:table frame="topbot"><oasis:tgroup cols="3">
     <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:thead>
       <oasis:row>
         <oasis:entry colname="col1">Time interval</oasis:entry>
         <oasis:entry colname="col2">CO<inline-formula><mml:math id="M314" display="inline"><mml:msub><mml:mi/><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mtext>OBS</mml:mtext></mml:mrow></mml:msub></mml:math></inline-formula> (ppm)</oasis:entry>
         <oasis:entry colname="col3"><inline-formula><mml:math id="M315" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula>CO<inline-formula><mml:math id="M316" display="inline"><mml:msub><mml:mi/><mml:mrow><mml:mn mathvariant="normal">2</mml:mn><mml:mo>,</mml:mo><mml:mtext>OBS</mml:mtext></mml:mrow></mml:msub></mml:math></inline-formula> (ppm)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">(<inline-formula><mml:math id="M317" display="inline"><mml:mrow><mml:msub><mml:mi>y</mml:mi><mml:mn mathvariant="normal">2</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>–<inline-formula><mml:math id="M318" display="inline"><mml:mrow><mml:msub><mml:mi>y</mml:mi><mml:mn mathvariant="normal">1</mml:mn></mml:msub></mml:mrow></mml:math></inline-formula>)</oasis:entry>
         <oasis:entry colname="col2">mean difference</oasis:entry>
         <oasis:entry colname="col3">mean difference</oasis:entry>
       </oasis:row>
       <oasis:row rowsep="1">
         <oasis:entry colname="col1"/>
         <oasis:entry colname="col2">(95 % CI)</oasis:entry>
         <oasis:entry colname="col3">(95 % CI)</oasis:entry>
       </oasis:row>
     </oasis:thead>
     <oasis:tbody>
       <oasis:row>
         <oasis:entry colname="col1">2006–2005</oasis:entry>
         <oasis:entry colname="col2">4.86 (4.5, 5.2)</oasis:entry>
         <oasis:entry colname="col3">2.08 (1.9, 2.3)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2007–2006</oasis:entry>
         <oasis:entry colname="col2">1.08 (0.69, 1.5)</oasis:entry>
         <oasis:entry colname="col3"><italic>0.0693</italic> <italic>(</italic><inline-formula><mml:math id="M319" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula><italic>0.15, 0.29)</italic></oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2008–2007</oasis:entry>
         <oasis:entry colname="col2">0.772 (0.37, 1.2)</oasis:entry>
         <oasis:entry colname="col3"><inline-formula><mml:math id="M320" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.43 (<inline-formula><mml:math id="M321" display="inline"><mml:mo lspace="0mm">-</mml:mo></mml:math></inline-formula>1.6, <inline-formula><mml:math id="M322" display="inline"><mml:mo>-</mml:mo></mml:math></inline-formula>1.2)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2009–2008</oasis:entry>
         <oasis:entry colname="col2">2.60 (2.2, 3.0)</oasis:entry>
         <oasis:entry colname="col3">1.12 (0.88, 1.4)</oasis:entry>
       </oasis:row>
       <oasis:row>
         <oasis:entry colname="col1">2009–2005</oasis:entry>
         <oasis:entry colname="col2">9.31 (8.9, 9.7)</oasis:entry>
         <oasis:entry colname="col3">1.84 (1.6, 2.0)</oasis:entry>
       </oasis:row>
     </oasis:tbody>
   </oasis:tgroup></oasis:table></table-wrap>

      <p id="d1e5347">As policy targets are often measured as relative changes over multiple
years, an important component of emissions inventories is their
ability to accurately capture multi-year changes. Observations
indicate enhancements above background <inline-formula><mml:math id="M323" 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> increased by
28 % (22 %, 34 %) between 2005 and 2009. ZHAO <inline-formula><mml:math id="M324" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM
estimates a 20 % increase over the same time period while
EDGAR <inline-formula><mml:math id="M325" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM and CDIAC <inline-formula><mml:math id="M326" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM estimate 61 % and 56 % increases
respectively.</p>
</sec>
<?pagebreak page3583?><sec id="Ch1.S4.SS5">
  <label>4.5</label><title>Implications for assessing national carbon emission targets</title>
      <p id="d1e5391">China has pledged a 60 %–65 % reduction in carbon intensity
by 2030 and has additionally set a benchmark of 40 %–45 %
reduction in carbon intensity by 2020, where both targets are relative
to the baseline year 2005 (NDRC, 2015; Guan et al., 2014). However,
Guan et al. (2014) found that provincial trends in carbon intensity
can vary significantly from national trends. Using the GRP values
shown in Fig. 9a, we calculate a northern China regional carbon
intensity incorporating the eight provinces encompassed significantly
by the L_0.90 region (Fig. 9c). We also estimate an L_0.90
regional carbon intensity based on the official national
energy-related <inline-formula><mml:math id="M327" 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> emissions in NDRC (2015); we scale the
national total by 39 % (35 %, 42 %), which is the mean
(range) contribution of the L_0.90 region to the national emissions
in 2005, averaged across the three unscaled gridded emissions
inventories.  We emphasize that carbon intensity values are inherently
uncertain due to complexities in GRP and GDP
calculations such as double-counting due to inter-provincial trade or
spatial mismatch between emissions and economic data. Nevertheless,
the analysis provides valuable insight into trends rather than precise
values.</p>
      <p id="d1e5405">Over the study time period, the GRP of the L_0.90 region more than
doubled (Fig. 9a), exhibiting a moderate, positive correlation with
the increasing trend in emissions (Fig. 9b). Coinciding with the 2008
Beijing Summer Olympics, the region's contribution to China's GDP grew
from approximately 13.5 % in 2007 to nearly 16 % in 2008,
representing a 20 % increase, before plateauing into 2009
(Fig. 9a). As noted in Guan et al. (2014), reductions in carbon
emissions intensity can come about via two main pathways: the first,
within industries, through increased energy efficiency combined with
expanded production capacity; the second, across the economy, through
structural shifts from energy-intensive industrial sectors to service
sectors. The doubling of GRP with the apparent reduction in regional
carbon intensity suggests a combination of enlarged production
capacity (including production of higher valued goods) and a shift
toward a service-oriented economy. In the former instance, a larger
production capacity tends to reduce the overall energy (and,
therefore, carbon) consumption of a single production unit. In the
latter instance, the energy consumption by the service sector is
considerably lower than that required by industrial and manufacturing
processes. In the northern China region, however, industry continues
to dominate the economy, suggesting that carbon intensity reductions
are more due to enlarged production capacity. From 2005 to 2009,
carbon intensity for the L_0.90 region decreased by 47 %
(28 %, 65 %), based on a one-sample <inline-formula><mml:math id="M328" display="inline"><mml:mi>t</mml:mi></mml:math></inline-formula> test of pooled
emissions intensity changes across scaled inventories. Analysis
presented by organizations such as the World Bank (World Bank, 2017)
suggests China's carbon intensity at the national level decreased by
20 % in 2009 relative to 2005. However, we note that the carbon
emissions data source for the World Bank carbon intensity calculations
is CDIAC. We have shown that at least for the L_0.90 region, CDIAC
emissions lead to significant underestimates of observations. Our work
here suggests that carbon accounting organizations such as the World
Bank would benefit from basing their national estimates for China on
a variety of inventories, incorporating increasingly available
China-specific approaches (including but not limited to MEIC and PKU),
EDGAR, and newer global inventories such as ODIAC. However, we
emphasize a crucial point with respect to the value of carbon
intensity targets, in agreement with Guan et al. (2014): carbon
intensity targets are especially misleading in developing countries
where absolute emissions continue to significantly grow in concert
with economic development goals. We see that despite the decreasing
carbon intensity of the region, pooled emissions estimates from the
three scaled inventories suggest an 18 % increase in absolute
emissions from 2005 to 2009 (Table 2, Fig. 9b). In terms of the climate
impact, it is the absolute carbon emissions rather than the carbon
intensity that ultimately matters.</p>
</sec>
</sec>
<sec id="Ch1.S5" sec-type="conclusions">
  <label>5</label><title>Conclusions</title>
      <?pagebreak page3584?><p id="d1e5424">Continuous hourly <inline-formula><mml:math id="M329" 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> observations, significantly influenced
by the heavily <inline-formula><mml:math id="M330" 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>-emitting northern China region, are used
in a top-down evaluation and scaling of three bottom-up <inline-formula><mml:math id="M331" 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>
flux inventories. We focus on the policy-relevant time interval from
2005 to 2009, noting that 2005 is China's baseline year for carbon
commitments. The three inventories are distinct in their anthropogenic
component, with a common biogenic flux component provided by the VPRM,
a simple satellite data-driven biosphere model calibrated with
ground-level ecosystem observations. The ZHAO anthropogenic emissions
inventory incorporates a regional approach to China's <inline-formula><mml:math id="M332" 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>
emissions estimation, using activity data at the provincial and
facility levels as well as domestic emission factors. The EDGAR and
CDIAC emissions inventories incorporate a greater reliance on global
averages and China's national statistics and international default
emission factors and depend more heavily on proxies (e.g.,
population) to allocate the emissions geographically. The three
anthropogenic inventories represent a range of methods used to
estimate emissions for China.</p>
      <p id="d1e5471">The northern China administrative region, excluding Inner Mongolia,
dominates the L_0.90 region, which is the region over which we
distribute the model–observation mismatch (Fig. 2). We find strong
seasonality in the L_0.90 region; the northwest features more
strongly in the non-growing season and there is a more symmetric
influence in the growing season. Within the L_0.90 region, EDGAR
and CDIAC are – on average across the 5 study years – lower than
ZHAO by 20 % and 36 %, respectively. Across administrative
regions, the highest discrepancy between the global and regional
inventories is in northern China, where the ZHAO inventory estimates
emissions that are on average 30 % higher than both EDGAR and
CDIAC (Table S1).</p>
      <p id="d1e5474">We find the ZHAO <inline-formula><mml:math id="M333" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM inventory generally agrees very closely with
observations, often significantly better than the nationally
referenced inventories at all timescales (hourly<?pagebreak page3585?> through annually),
with the exception of the peak growing season. During the peak growing
season, the regional enhancement to background <inline-formula><mml:math id="M334" 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>
concentrations is modeled as approximately zero, due to an
agriculturally dominated vegetation signal that is equal in magnitude
and opposite in sign to the anthropogenic signal (Dayalu et al.,
2018a). While this agrees with previous work by Turnbull et al. (2011),
in both that study and the present study the sparse data prevent
a more conclusive statement about anthropogenic inventory performance
during the regional growing season. At annual timescales, the
anthropogenic signal dominates, and we find that emission rates from
EDGAR and CDIAC lead to underestimated emissions in the northern China
region by an average of 30 % and 70 %, respectively, averaged
across all study years. We note that the discrepancy between the
EDGAR-based time series and the observations generally decreases over
the 5-year study period. In contrast, emission rates from the ZHAO
inventory gives a priori results very close to observations
throughout and is not significantly affected by the scaling: the error
bars for the scaled estimates consistently include the original
estimate. Note that the EDGAR and CDIAC inventories can differ from
<inline-formula><mml:math id="M335" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">10</mml:mn></mml:mrow></mml:math></inline-formula> % to <inline-formula><mml:math id="M336" display="inline"><mml:mrow><mml:mo>-</mml:mo><mml:mn mathvariant="normal">20</mml:mn></mml:mrow></mml:math></inline-formula> % relative to ZHAO in their national
emissions totals (Table S1).  The inventories evaluated here exhibit
distinct differences in their ability to match observations. However,
observational data from a network of sites strategically located in
and around the eastern half of China would be required to (1) examine
whether differences in spatial allocation approaches contribute to
differences among the inventories and (2) conduct actual optimizations
of the inventories.</p>
      <p id="d1e5515">We find that carbon intensity in the region has decreased by
47 %(28 %, 65 %) from 2005 to 2009, from approximately
4 <inline-formula><mml:math id="M337" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi></mml:mrow></mml:math></inline-formula> of <inline-formula><mml:math id="M338" 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> per USD in 2005 to about
2 <inline-formula><mml:math id="M339" display="inline"><mml:mrow class="unit"><mml:mi mathvariant="normal">kg</mml:mi></mml:mrow></mml:math></inline-formula> of <inline-formula><mml:math id="M340" 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> per USD in 2009 (Fig. 9c). However, we
see that despite the decreasing carbon intensity of the region, there
is an 18 % increase in absolute emissions over time, affirming the
point made by Guan et al. (2014) that meeting carbon intensity targets
in emerging economies can be at odds with making real climate progress
(Table 2, Fig. 9b).</p>
      <p id="d1e5557">Despite the limitations of having data from a single site, this
analysis demonstrates how a long time series of continuous
observations can identify apparent overall biases in some
inventories. Our results, while specific to northern China regional
emissions in particular, also provide some insight into current
methods of carbon emissions accounting for China as a whole. We
emphasize that this work is intended to be a comparison of emission
rates from a subset of anthropogenic <inline-formula><mml:math id="M341" 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> inventories over
northern China that were readily available at the time this research
began and is not intended to be an advocate or criticism of any single
published inventory. Rather, we use a long 60-month continuous
observational record to examine model–data mismatch in an important
carbon-emitting region where local data are difficult to access and
global datasets are forced to rely on the best available public data,
which are not necessarily accurate assumptions of China-specific
activity. Second, while we recognize the height limitations – and
therefore the footprint – of the Miyun receptor, its topographic
advantage along with the low-productivity vicinity makes it similar to
other short-tower sites suitable for regional analysis. In addition,
a detailed assessment of uncertainty stemming from errors in
transport, biogenic inventories, and inventory spatial allocation
remains a challenge.  Independent verification from concurrent
aircraft measurements (for example) or multi-level inlet locations
were not available to quantify the impact of absolute and relative
inlet location on transport uncertainty. Finally, we emphasize our
implied seasonal and annual “corrections”, or scalings, of modeled
<inline-formula><mml:math id="M342" 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> relative to observations are not optimizations; rather,
they simply reflect the extent to which the individual
anthropogenic <inline-formula><mml:math id="M343" display="inline"><mml:mo>+</mml:mo></mml:math></inline-formula> VPRM <inline-formula><mml:math id="M344" 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> flux models deviate from the
observations. At least in the winter, where biogenic processes are at
a minimum, the low bias of ZHAO-modeled <inline-formula><mml:math id="M345" 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> concentrations
suggests the ZHAO inventory is closer to actual emissions. However,
improved representation of temporal anthropogenic activity factors and
biosphere processes are needed to extend the conclusions of
anthropogenic inventory performance to all seasons.  Effectively
evaluating and constraining inventory emissions rates at relevant
spatial scales requires multiple stations of high-temporal-resolution
observations, as well as improvements and greater diversity in
observationally constrained biogenic flux models. In its current
configuration, the single biogenic flux model precludes
a comprehensive multi-seasonal and annual disentangling of
contributions to <inline-formula><mml:math id="M346" 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>; particularly in our annual scale
analysis, we are ascribing more uncertainty to the anthropogenic
inventories over the biogenic contributions. Absent data from a dense
network of ecosystem flux and atmospheric measurements, there will
constantly be a tradeoff between drawing conclusions using
low-temporal-resolution flask measurements from a few sites and
continuous data from a single location.</p>
      <p id="d1e5623">In situ <inline-formula><mml:math id="M347" 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> observations interpreted within
a high-resolution model framework such as that described in this study
provide a powerful constraint to test and correct spatially explicit
inventories. The observation station available for the 2005–2009
period was strategically located to provide information on one of the
highest <inline-formula><mml:math id="M348" 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>-emitting regions of China. Within the
limitations described above, the observations provide strong evidence
supporting the use of China-specific methods, such as those employed
in ZHAO, for China's <inline-formula><mml:math id="M349" 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> emissions inventory derivation. In
future, access to a spatially dense network of measurements will allow
for a sophisticated error analysis that can more readily assess
uncertainty in key model components such as transport, flux fields,
and background concentrations.  Along with the results presented here,
previous studies (e.g., Turnbull et al., 2011) provide key information
that is necessary to guide and motivate more extensive future
measurement and emissions evaluation efforts. Such future efforts will
benefit substantially from incorporating newly available information
from column-average <inline-formula><mml:math id="M350" 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> concentrations acquired by<?pagebreak page3586?> orbiting
instruments or ground-based spectrometers to increase observational
coverage. A number of existing (OCO-2, OCO-3) and planned satellite
missions will significantly reduce the observational gap in China,
though surface observations provide additional constraints and a link
to absolute calibration scales. A denser network of <inline-formula><mml:math id="M351" 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>
measurement stations in China is required as a component for effective
monitoring, reporting, and verification of regional and national
inventories. The results of this research present a necessary baseline
for a key <inline-formula><mml:math id="M352" 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>-emitting region of China. Our results have
broad implications for designing future analyses as more
observations of China's <inline-formula><mml:math id="M353" 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> continue to become available,
particularly in the era of increased <inline-formula><mml:math id="M354" 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> satellite
coverage. However, as the quality of satellite retrievals can be
compromised by factors such as aerosol loading, surface observations
continue to be crucial for the region both in their own right and as
a key component of cross-platform evaluations.</p>
</sec>

      
      </body>
    <back><notes notes-type="codedataavailability"><title>Code and data availability</title>

      <p id="d1e5719">Code and data are available through the Harvard Dataverse at <ext-link xlink:href="https://doi.org/10.7910/DVN/OJESO0" ext-link-type="DOI">10.7910/DVN/OJESO0</ext-link> (Dayalu et al., 2018b). The code and data Supplement includes
observational and modeled <inline-formula><mml:math id="M355" 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> time series, WRF and STILT parameter
files, and STILT footprint files.</p>
  </notes><app-group>
        <supplementary-material position="anchor"><p id="d1e5736">The supplement related to this article is available online at: <inline-supplementary-material xlink:href="https://doi.org/10.5194/acp-20-3569-2020-supplement" xlink:title="pdf">https://doi.org/10.5194/acp-20-3569-2020-supplement</inline-supplementary-material>.</p></supplementary-material>
        </app-group><notes notes-type="authorcontribution"><title>Author contributions</title>

      <p id="d1e5745">AD, JWM, and SCW designed the research. AD performed the research
with guidance from all co-authors. YW and JWM monitored, maintained, and
provided access to the Miyun hourly observational dataset. YZ provided
the China-specific anthropogenic inventory. WRF-STILT simulations were
performed by AD with assistance from TN. AD constructed the vegetation
<inline-formula><mml:math id="M356" 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> inventory. AD and JWM wrote the paper with contributions from
all other co-authors.</p>
  </notes><notes notes-type="competinginterests"><title>Competing interests</title>

      <p id="d1e5762">The authors declare that they have no conflict of interest.</p>
  </notes><ack><title>Acknowledgements</title><p id="d1e5768">We thank Zhiming Kuang for providing computational
resources. We also thank Jenna Samra, Maryann Sargent, and Victoria Liublinska for helpful discussion.</p></ack><notes notes-type="financialsupport"><title>Financial support</title>

      <p id="d1e5773">This research has been supported by the Harvard-China Project and the Harvard Global Institute.</p>
  </notes><notes notes-type="reviewstatement"><title>Review statement</title>

      <p id="d1e5779">This paper was edited by Christoph Gerbig and reviewed by two anonymous referees.</p>
  </notes><ref-list>
    <title>References</title>

      <ref id="bib1.bib1"><label>1</label><?label 1?><mixed-citation>Andres, R. J., Boden, T. A., and Marland, G.: Annual Fossil-Fuel <inline-formula><mml:math id="M357" 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>
Emissions: Mass of Emissions Gridded by One Degree Latitude by One Degree
Longitude v2016. Carbon Dioxide Information Analysis Center, Oak Ridge
National Laboratory, US Department of Energy, Oak Ridge, Tenn., USA, <ext-link xlink:href="https://doi.org/10.3334/CDIAC/ffe.ndp058.2016" ext-link-type="DOI">10.3334/CDIAC/ffe.ndp058.2016</ext-link>, 2016a.</mixed-citation></ref>
      <ref id="bib1.bib2"><label>2</label><?label 2?><mixed-citation>Andres, R. J., Boden, T. A., and Higdon, D. M.: Gridded uncertainty in fossil fuel carbon dioxide emission maps, a CDIAC example, Atmos. Chem. Phys., 16, 14979–14995, <ext-link xlink:href="https://doi.org/10.5194/acp-16-14979-2016" ext-link-type="DOI">10.5194/acp-16-14979-2016</ext-link>, 2016b.</mixed-citation></ref>
      <ref id="bib1.bib3"><label>3</label><?label 3?><mixed-citation>Boden, T. A., Marland, G., and Andres, R. J.: Global, Regional, and National
Fossil-Fuel <inline-formula><mml:math id="M358" 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> Emissions. Carbon Dioxide Information Analysis Center,
Oak Ridge National Laboratory, US Department of Energy, Oak Ridge, Tenn., USA, <ext-link xlink:href="https://doi.org/10.3334/CDIAC/00001_V2016" ext-link-type="DOI">10.3334/CDIAC/00001_V2016</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib4"><label>4</label><?label 4?><mixed-citation>Brown, D., Brownrigg, R., Haley, M., and Huang, W.:  The NCAR Command Language (NCL) v6.0. 0, UCAR/NCAR Computational
and Information Systems Laboratory, Boulder, CO, <ext-link xlink:href="https://doi.org/10.5065/D6WD3XH5" ext-link-type="DOI">10.5065/D6WD3XH5</ext-link>, 2012.</mixed-citation></ref>
      <ref id="bib1.bib5"><label>5</label><?label 5?><mixed-citation>
Dayalu, A.: Exploring the Wide Net of Human Energy Systems: From
Carbon Dioxide Emissions in China to Hydraulic Fracturing Chemicals Usage in
the United States, PhD thesis, Harvard University, Cambridge, MA, 2017.</mixed-citation></ref>
      <ref id="bib1.bib6"><label>6</label><?label 6?><mixed-citation>Dayalu, A., Munger, J. W., Wofsy, S. C., Wang, Y., Nehrkorn, T., Zhao, Y., McElroy, M. B., Nielsen, C. P., and Luus, K.: Assessing biotic contributions to <inline-formula><mml:math id="M359" 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> fluxes in northern China using the Vegetation, Photosynthesis and Respiration Model (VPRM-CHINA) and observations from 2005 to 2009, Biogeosciences, 15, 6713–6729, <ext-link xlink:href="https://doi.org/10.5194/bg-15-6713-2018" ext-link-type="DOI">10.5194/bg-15-6713-2018</ext-link>, 2018a.</mixed-citation></ref>
      <ref id="bib1.bib7"><label>7</label><?label 6a?><mixed-citation>Dayalu, A., Munger,  J. W., Wang,  Y., Wofsy,  S. C., Zhao,  Y., Nehrkorn,  T., Nielsen,  C., McElroy,  M. B., and Chang,  R.: Replication Data for: Evaluating China's anthropogenic <inline-formula><mml:math id="M360" 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> emissions inventories: a northern China case-study using continuous surface observations from 2005–2009, <ext-link xlink:href="https://doi.org/10.7910/DVN/OJESO0" ext-link-type="DOI">10.7910/DVN/OJESO0</ext-link>, 2018b.</mixed-citation></ref>
      <ref id="bib1.bib8"><label>8</label><?label 7?><mixed-citation>European Commission, Joint Research Centre (JRC)/Netherlands Environmental
Assessment Agency (PBL): Emission Database for Global Atmospheric Research
(EDGAR), release EDGARv4.2 FT2010, available at: <uri>http://edgar.jrc.ec.europa.eu</uri> (last access: 13 March 2017),
2013.</mixed-citation></ref>
      <ref id="bib1.bib9"><label>9</label><?label 8?><mixed-citation>Guan, D., Liu, Z., Geng, Y., Lindner, S., and Hubacek, K.: The gigatonne gap
in China's carbon dioxide inventories, Nat. Clim. Change, 2, 672–675,
<ext-link xlink:href="https://doi.org/10.1038/nclimate1560" ext-link-type="DOI">10.1038/nclimate1560</ext-link>, 2012.</mixed-citation></ref>
      <ref id="bib1.bib10"><label>10</label><?label 9?><mixed-citation>Guan, D., Klasen, S., Hubacek, K., Feng, K., Liu, Z., He, K., Geng, Y., and
Zhang Q.: Determinants of stagnating carbon intensity in China, Nat. Clim.
Change, 4, 1017–1023, <ext-link xlink:href="https://doi.org/10.1038/nclimate2388" ext-link-type="DOI">10.1038/nclimate2388</ext-link>, 2014.</mixed-citation></ref>
      <ref id="bib1.bib11"><label>11</label><?label 10a?><mixed-citation>Jiang, F., Chen, J., Zhou, L., Ju, W., Zhang, H., Machida, T., Ciais, P., Peters, W., Wang, H., Chen, B., Liu, L., Zhang, C., Matsueda, H., and Sawa, Y.: A comprehensive estimate of recent carbon sinks in China using both top-down and bottom-up approaches, Sci. Rep.-UK, 6, 22130, <ext-link xlink:href="https://doi.org/10.1038/srep22130" ext-link-type="DOI">10.1038/srep22130</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib12"><label>12</label><?label 11?><mixed-citation>Karion, A., Sweeney, C., Miller, J. B., Andrews, A. E., Commane, R., Dinardo, S., Henderson, J. M., Lindaas, J., Lin, J. C., Luus, K. A., Newberger, T., Tans, P., Wofsy, S. C., Wolter, S<?pagebreak page3587?>., and Miller, C. E.: Investigating Alaskan methane and carbon dioxide fluxes using measurements from the CARVE tower, Atmos. Chem. Phys., 16, 5383–5398, <ext-link xlink:href="https://doi.org/10.5194/acp-16-5383-2016" ext-link-type="DOI">10.5194/acp-16-5383-2016</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib13"><label>13</label><?label 12?><mixed-citation>Kort, E. A., Angevine, W. M., Duren, R., and Miller, C. E.: Surface
observations for monitoring urban fossil fuel <inline-formula><mml:math id="M361" 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> emissions: Minimum
site location requirements for the Los Angeles megacity, J. Geophys. Res.-Atmos., 118, 1577–1584, <ext-link xlink:href="https://doi.org/10.1002/jgrd.50135" ext-link-type="DOI">10.1002/jgrd.50135</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib14"><label>14</label><?label 13?><mixed-citation>Le Quéré, C., Andrew, R. M., Canadell, J. G., Sitch, S., Korsbakken, J. I., Peters, G. P., Manning, A. C., Boden, T. A., Tans, P. P., Houghton, R. A., Keeling, R. F., Alin, S., Andrews, O. D., Anthoni, P., Barbero, L., Bopp, L., Chevallier, F., Chini, L. P., Ciais, P., Currie, K., Delire, C., Doney, S. C., Friedlingstein, P., Gkritzalis, T., Harris, I., Hauck, J., Haverd, V., Hoppema, M., Klein Goldewijk, K., Jain, A. K., Kato, E., Körtzinger, A., Landschützer, P., Lefèvre, N., Lenton, A., Lienert, S., Lombardozzi, D., Melton, J. R., Metzl, N., Millero, F., Monteiro, P. M. S., Munro, D. R., Nabel, J. E. M. S., Nakaoka, S., O'Brien, K., Olsen, A., Omar, A. M., Ono, T., Pierrot, D., Poulter, B., Rödenbeck, C., Salisbury, J., Schuster, U., Schwinger, J., Séférian, R., Skjelvan, I., Stocker, B. D., Sutton, A. J., Takahashi, T., Tian, H., Tilbrook, B., van der Laan-Luijkx, I. T., van der Werf, G. R., Viovy, N., Walker, A. P., Wiltshire, A. J., and Zaehle, S.: Global Carbon Budget 2016, Earth Syst. Sci. Data, 8, 605–649, <ext-link xlink:href="https://doi.org/10.5194/essd-8-605-2016" ext-link-type="DOI">10.5194/essd-8-605-2016</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib15"><label>15</label><?label 14?><mixed-citation>Lin, J. C., Gerbig, C., Wofsy, S. C., Andrews, A. E., Daube, B. C., Davis, K. J., and Grainger, C. A.: A near-field tool for simulating the upstream
influence of atmospheric observations: The Stochastic Time-Inverted
Lagrangian Transport (STILT) model, J. Geophys.
Res.-Atmos., 108, 4493, <ext-link xlink:href="https://doi.org/10.1029/2002JD003161" ext-link-type="DOI">10.1029/2002JD003161</ext-link>, 2003.</mixed-citation></ref>
      <ref id="bib1.bib16"><label>16</label><?label 15?><mixed-citation>
Liu, Z., Guan, D., Wei, W., Davis, S. J., Ciais, P., Bai, J., Peng, S.,
Zhang, Q., Hubacek, K., Marland, G., Andres, R. J., Crawford-Brown, D., Lin, J., Zhao, H., Hong, C., Boden, T. A., Feng, K., Peters, G. P., Xi, F., Liu, J., Li, Y., Zhao, Y., Zeng, N., and He, K.:  Reduced carbon emission
estimates from fossil fuel combustion and cement production in China, Nature,
524, 335–338, 2015.</mixed-citation></ref>
      <ref id="bib1.bib17"><label>17</label><?label 16?><mixed-citation>Mahadevan, P., Wofsy, S. C., Matross, D. M., Xiao, X., Dunn, A. L.,
Lin, J. C., Gerbig, C., Munger, J. W., Chow, V. Y., and Gottlieb, E. W.: A satellite-based biosphere parameterization for net ecosystem <inline-formula><mml:math id="M362" 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> exchange:
Vegetation Photosynthesis and Respiration Model (VPRM), Global Biogeochem.
Cy., 22, GB2005, <ext-link xlink:href="https://doi.org/10.1029/2006GB002735" ext-link-type="DOI">10.1029/2006GB002735</ext-link>, 2008.</mixed-citation></ref>
      <ref id="bib1.bib18"><label>18</label><?label 17?><mixed-citation>
Matross, D. M., Andrews, A., Pathmathevan, M., Gerbig, C., Lin, J. C.,
Wofsy, S. C., Daube, B. C., Gottlieb, E. W., Chow, V. Y., Lee, J. T., Zhao, C. L., Bakwin, P. S., Munger, J. W., and Hollinger, D. Y.: Estimating
regional carbon exchange in New England and Quebec by combining atmospheric,
ground-based and satellite data, Tellus B, 58, 344–358, 2006.</mixed-citation></ref>
      <ref id="bib1.bib19"><label>19</label><?label 19?><mixed-citation>
McKain, K., Wofsy, S. C., Nehrkorn, T., Eluszkiewicz, Ehleringer, J. R., and
Stephens, B. B.: Assessment of ground-based atmospheric observations for
verification of greenhouse gas emissions from an urban region, P. Natl.
Acad. Sci. USA, 109, 8423–8428, 2012.</mixed-citation></ref>
      <ref id="bib1.bib20"><label>20</label><?label 18?><mixed-citation>
McKain, K., Down, A., Raciti, S. M., Budney, J., Hutyra, L. R.,
Floerchinger, C., Herndon, S. C., Nehrkorn, T., Zahniser, M. S., and
Jackson, R. B.: Methane emissions from natural gas infrastructure and use in
the urban region of Boston, Massachusetts, P. Natl. Acad. Sci. USA, 112,
1941–1946, 2015.</mixed-citation></ref>
      <ref id="bib1.bib21"><label>21</label><?label 20?><mixed-citation>Miller, S. M., Kort, E. A., Hirsch, A. I., Dlugokencky, E. J., Andrews, A. E.,
Xu, X., Tian, H., Nehrkorn, T. Eluszkiewicz, J., Michalak, A. M., and Wofsy, S. C.: Regional sources of nitrous oxide over the United States: Seasonal
variation and spatial distribution, J. Geophys. Res., 117, D06310,
<ext-link xlink:href="https://doi.org/10.1029/2011JD016951" ext-link-type="DOI">10.1029/2011JD016951</ext-link>, 2012.</mixed-citation></ref>
      <ref id="bib1.bib22"><label>22</label><?label 21?><mixed-citation>Nassar, R., Napier-Linton, L., Gurney, K. R., Andres, R. J., Oda, T., Vogel, F. R., and Deng, F.: Improving the temporal and spatial distribution of
<inline-formula><mml:math id="M363" 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> emissions from global fossil fuel emission data sets, J. Geophys.
Res.-Atmos., 118, 917–933, <ext-link xlink:href="https://doi.org/10.1029/2012JD018196" ext-link-type="DOI">10.1029/2012JD018196</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib23"><label>23</label><?label 24?><mixed-citation>NCEP National Centers for Environmental Prediction/National Weather
Service/NOAA/US Department of Commerce: NCEP FNL Operational Model Global Tropospheric
Analyses, continuing from July 1999, <ext-link xlink:href="https://doi.org/10.5065/D6M043C6" ext-link-type="DOI">10.5065/D6M043C6</ext-link>,
Research Data Archive at the National Center for Atmospheric Research,
Computational and Information Systems Laboratory, Boulder, Co., updated
daily,  2000.</mixed-citation></ref>
      <ref id="bib1.bib24"><label>24</label><?label 26?><mixed-citation>NDRC National Development Reform Commission: Enhanced Actions on Climate
Change: China's Intended Nationally Determined Contributions,  Beijing, China, available at: <uri>https://www4.unfccc.int/sites/ndcstaging/PublishedDocuments/China%20First/China%27s%20First%20NDC%20Submission.pdf</uri> (last access: 20 March 2020), 2015.</mixed-citation></ref>
      <ref id="bib1.bib25"><label>25</label><?label 27?><mixed-citation>Nehrkorn, T., Eluszkiewicz, J., Wofsy, S. C., Lin, J., Gerbig, C., Longo, M.,
and Freitas, S.: Coupled weather research and forecasting–stochastic
time-inverted lagrangian transport (WRF–STILT) model, Meteorol. Atmos.
Phys., 107, 51–64,  <ext-link xlink:href="https://doi.org/10.1007/s00703-010-0068-x" ext-link-type="DOI">10.1007/s00703-010-0068-x</ext-link>, 2010.</mixed-citation></ref>
      <ref id="bib1.bib26"><label>26</label><?label 22?><mixed-citation>Nielsen, C. and Ho, M.: Clearer Skies Over China: Reconciling Air Quality,
Climate, and Economic Goals, MIT Press, ISBN 9780262019880, Cambridge, Mass., USA,
<ext-link xlink:href="https://doi.org/10.7551/mitpress/9780262019880.001.0001" ext-link-type="DOI">10.7551/mitpress/9780262019880.001.0001</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib27"><label>27</label><?label 23?><mixed-citation>Niu, Z., Zhou, W., Wu, S., Cheng, P., Lu, X., Xiong, X., Du, H., Fu, Y., and
Wang, G.: Atmospheric Fossil Fuel <inline-formula><mml:math id="M364" 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> Traced by <inline-formula><mml:math id="M365" display="inline"><mml:mi mathvariant="normal">Δ</mml:mi></mml:math></inline-formula><inline-formula><mml:math id="M366" display="inline"><mml:msup><mml:mi/><mml:mn mathvariant="normal">14</mml:mn></mml:msup></mml:math></inline-formula>C in Beijing and
Xiamen, China: Temporal Variations, Inland/Coastal Differences and
Influencing Factors, Environ. Sci. Technol., 50, 5474–5480, <ext-link xlink:href="https://doi.org/10.1021/acs.est.5b02591" ext-link-type="DOI">10.1021/acs.est.5b02591</ext-link>, 2016</mixed-citation></ref>
      <ref id="bib1.bib28"><label>28</label><?label 28?><mixed-citation>Oda, T., Maksyutov, S., and Andres, R. J.: The Open-source Data Inventory for
Anthropogenic <inline-formula><mml:math id="M367" 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>, version 2016 (ODIAC2016): a global monthly fossil fuel <inline-formula><mml:math id="M368" 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>
gridded emissions data product for tracer transport simulations and surface
flux inversions, Earth Syst. Sci. Data, 10, 87–107,
<ext-link xlink:href="https://doi.org/10.5194/essd-10-87-2018" ext-link-type="DOI">10.5194/essd-10-87-2018</ext-link>, 2018.</mixed-citation></ref>
      <ref id="bib1.bib29"><label>29</label><?label 29?><mixed-citation>
Piao, S., Fang, J., Ciais, P., Peylin, P., Huang, Y., Sitch, S., and Wang, T.: The carbon balance of terrestrial ecosystems in China, Nature,
458, 1009–1013, 2009.</mixed-citation></ref>
      <ref id="bib1.bib30"><label>30</label><?label 30?><mixed-citation>Sargent, M., Barrera, Y., Nehrkorn, T., Hutyra, L., Gately, C., Jones, T.,
McKain, K., Sweeney, C., Hegarty, J., Hardiman, B., Wang, J., and Wofsy, S.:
Anthropogenic and biogenic <inline-formula><mml:math id="M369" 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> fluxes in the Boston urban region, P.
Natl. Acad. Sci. USA, 115, 7491–7496, <ext-link xlink:href="https://doi.org/10.1073/pnas.1803715115" ext-link-type="DOI">10.1073/pnas.1803715115</ext-link>,
2018.</mixed-citation></ref>
      <ref id="bib1.bib31"><label>31</label><?label 31?><mixed-citation>Shan, Y., Liu, J., Liu, Z., Xu, X., Shao, S., Wang, P., and Guan, D.: New
provincial <inline-formula><mml:math id="M370" 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> emission inventories in China based on apparent energy
consumption da<?pagebreak page3588?>ta and updated emission factors, Appl. Energ., 184,
742–750, <ext-link xlink:href="https://doi.org/10.1016/j.apenergy.2016.03.073" ext-link-type="DOI">10.1016/j.apenergy.2016.03.073</ext-link>, 2016.</mixed-citation></ref>
      <ref id="bib1.bib32"><label>32</label><?label 32?><mixed-citation>Turnbull, J. C., Tans, P. P., Lehman, S. J., Baker, D., Chung, Y., Gregg, J. S.,
Miller, J. B., Southon, J. R., and Zhao, L.: Atmospheric observations of carbon
monoxide and fossil fuel <inline-formula><mml:math id="M371" 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> emissions from East Asia, J. Geophys. Res.-Atmos., 116, D24306, <ext-link xlink:href="https://doi.org/10.1029/2011JD016691" ext-link-type="DOI">10.1029/2011JD016691</ext-link>, 2011.</mixed-citation></ref>
      <ref id="bib1.bib33"><label>33</label><?label 33?><mixed-citation>Ummel, K.: CARMA Revisited: An Updated Database of Carbon Dioxide Emissions
from Power Plants Worldwide, CGD Working Paper 304,
Center for Global Development, Washington, DC, available at:
<uri>http://www.cgdev.org/content/publications/detail/1426429</uri> (last access: 20 March 2020),
2012.</mixed-citation></ref>
      <ref id="bib1.bib34"><label>34</label><?label 33a?><mixed-citation>US EIA (US Energy Information Administration: Total Carbon Dioxide Emissions from the Consumption of
Energy, available at: <uri>https://www.eia.gov/beta/international/data/browser</uri>, last access: 12 January 2017.</mixed-citation></ref>
      <ref id="bib1.bib35"><label>35</label><?label 34?><mixed-citation>Wang, R., Tao, S., Ciais, P., Shen, H. Z., Huang, Y., Chen, H., Shen, G. F., Wang, B., Li, W., Zhang, Y. Y., Lu, Y., Zhu, D., Chen, Y. C., Liu, X. P., Wang, W. T., Wang, X. L., Liu, W. X., Li, B. G., and Piao, S. L.: High-resolution mapping of combustion processes and implications for <inline-formula><mml:math id="M372" 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> emissions, Atmos. Chem. Phys., 13, 5189–5203, <ext-link xlink:href="https://doi.org/10.5194/acp-13-5189-2013" ext-link-type="DOI">10.5194/acp-13-5189-2013</ext-link>, 2013.</mixed-citation></ref>
      <ref id="bib1.bib36"><label>36</label><?label 35?><mixed-citation>Wang, X., Wang, Y. X., Hao, J. M., Kondo, Y., Irwin, M., Munger, J. W., and
Zhao, Y. J.: Top-down estimate of China's black carbon emissions using surface
observations: Sensitivity to observation representativeness and transport
model error, J. Geophys. Res.-Atmos., 118, 5781–5795, <ext-link xlink:href="https://doi.org/10.1002/jgrd.50397" ext-link-type="DOI">10.1002/jgrd.50397</ext-link>. 2013.
</mixed-citation></ref><?xmltex \hack{\newpage}?>
      <ref id="bib1.bib37"><label>37</label><?label 37?><mixed-citation>Wang, Y., Munger, J. W., Xu, S., McElroy, M. B., Hao, J., Nielsen, C. P., and Ma, H.: <inline-formula><mml:math id="M373" 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 its correlation with CO at a rural site near Beijing: implications for combustion efficiency in China, Atmos. Chem. Phys., 10, 8881–8897, <ext-link xlink:href="https://doi.org/10.5194/acp-10-8881-2010" ext-link-type="DOI">10.5194/acp-10-8881-2010</ext-link>, 2010.</mixed-citation></ref>
      <ref id="bib1.bib38"><label>38</label><?label 36?><mixed-citation>Wang, Y., Wang, X., Kondo, Y., Kajino, M., Munger, J. W., and Hao, J.: Black
carbon and its correlation with trace gases at a rural site in Beijing:
Top-down constraints from ambient measurements on bottom-up emissions,
J. Geophys. Res.-Atmos., 116, D24304, <ext-link xlink:href="https://doi.org/10.1029/2011jd016575" ext-link-type="DOI">10.1029/2011jd016575</ext-link>, 2011.</mixed-citation></ref>
      <ref id="bib1.bib39"><label>39</label><?label 38?><mixed-citation>World Bank:  <inline-formula><mml:math id="M374" 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> emissions (kg per PPP $ of GDP), available at:
<uri>https://data.worldbank.org/indicator/EN.ATM.CO2E.PP.GD?locations=CN</uri>,
last access: 12 May 2017.</mixed-citation></ref>
      <ref id="bib1.bib40"><label>40</label><?label 39?><mixed-citation>Zhao, Y., Nielsen, C. P., and McElroy, M.: China's <inline-formula><mml:math id="M375" 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> emissions
estimated from the bottom up: Recent trends, spatial distributions, and
quantification of uncertainties, Atmos. Environ., 59, 214–223, 2012.</mixed-citation></ref>
      <ref id="bib1.bib41"><label>41</label><?label 40?><mixed-citation>Zhao, Y., Zhang, J., and Nielsen, C. P.: The effects of recent control policies on trends in emissions of anthropogenic atmospheric pollutants and <inline-formula><mml:math id="M376" 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> in China, Atmos. Chem. Phys., 13, 487–508, <ext-link xlink:href="https://doi.org/10.5194/acp-13-487-2013" ext-link-type="DOI">10.5194/acp-13-487-2013</ext-link>, 2013.</mixed-citation></ref>

  </ref-list></back>
    <!--<article-title-html>Evaluating China's anthropogenic CO<sub>2</sub> emissions inventories: a northern China case study using continuous surface observations from 2005 to 2009</article-title-html>
<abstract-html><p>China has pledged reduction of carbon dioxide (CO<sub>2</sub>)
emissions per unit of gross domestic product (GDP) by 60&thinsp;%–65&thinsp;% relative to 2005 levels,
and to peak carbon emissions overall by 2030. However, the lack of
observational data and disagreement among the many available
inventories makes it difficult for China to track progress toward
these goals and evaluate the efficacy of control measures. To
demonstrate the value of atmospheric observations for constraining
CO<sub>2</sub> inventories we track the ability of CO<sub>2</sub>
concentrations predicted from three different CO<sub>2</sub>
inventories to match a unique multi-year continuous record of
atmospheric CO<sub>2</sub>. Our analysis time window includes the key
commitment period for the Paris Agreement (2005) and the Beijing
Olympics (2008). One inventory is China-specific and two are spatial
subsets of global inventories. The inventories differ in spatial
resolution, basis in national or subnational statistics, and reliance
on global or China-specific emission factors. We use a unique set of
historical atmospheric observations from 2005 to 2009 to evaluate the
three CO<sub>2</sub> emissions inventories within China's heavily
industrialized and populated northern region accounting for
 ∼ 33&thinsp;%–41&thinsp;% of national emissions. Each anthropogenic
inventory is combined with estimates of biogenic CO<sub>2</sub> within
a high-resolution atmospheric transport framework to model the time
series of CO<sub>2</sub> observations. To convert the model–observation
mismatch from mixing ratio to mass emission rates we distribute it
over a region encompassing 90&thinsp;% of the total surface influence in
seasonal (annual) averaged back-trajectory footprints (L_0.90
region). The L_0.90 region roughly corresponds to northern
China. Except for the peak growing season, where assessment of
anthropogenic emissions is entangled with the strong vegetation
signal, we find the China-specific inventory based on subnational data
and domestic field studies agrees significantly better with
observations than the global inventories at all timescales. Averaged
over the study time period, the unscaled China-specific inventory
reports substantially larger annual emissions for northern China
(30&thinsp;%) and China as a whole (20&thinsp;%) than the two unscaled
global inventories. Our results, exploiting a robust time series of
continuous observations, lend support to the rates and geographic
distribution in the China-specific inventory Though even long-term
observations at a single site reveal differences among inventories,
exploring inventory discrepancy over all of China requires a denser
observational network in future efforts to measure and verify
CO<sub>2</sub> emissions for China both regionally and nationally. We
find that carbon intensity in the northern China region has decreased
by 47&thinsp;% from 2005 to 2009, from approximately
4&thinsp;kg of CO<sub>2</sub> per USD (note that all references to USD in this paper refer to USD adjusted for purchasing power parity, PPP) in 2005 to about
2&thinsp;kg of CO<sub>2</sub> per USD in 2009
(Fig. 9c). However, the corresponding 18&thinsp;% increase in
absolute emissions over the same time period affirms a critical point
that carbon intensity targets in emerging economies can be at odds
with making real climate progress. Our results provide an important
quantification of model–observation mismatch, supporting the increased
use and development of China-specific inventories in tracking China's
progress as a whole towards reducing emissions. We emphasize that this
work presents a methodology for extending the analysis to other
inventories and is intended to be a comparison of a subset of
anthropogenic CO<sub>2</sub> emissions rates from inventories that were
readily available at the time this research began. For this study's
analysis time period, there was not enough spatially distinct
observational data to conduct an optimization of the inventories.  The
primary intent of the comparisons presented here is not to judge
specific inventories, but to demonstrate that even a single site with
a long record of high-time-resolution observations can identify major
differences among inventories that manifest as biases in the
model–data comparison. This study provides a baseline analysis for
evaluating emissions from a small but important region within China,
as well a guide for determining optimal locations for future
ground-based measurement sites.</p></abstract-html>
<ref-html id="bib1.bib1"><label>1</label><mixed-citation>
Andres, R. J., Boden, T. A., and Marland, G.: Annual Fossil-Fuel CO<sub>2</sub>
Emissions: Mass of Emissions Gridded by One Degree Latitude by One Degree
Longitude v2016. Carbon Dioxide Information Analysis Center, Oak Ridge
National Laboratory, US Department of Energy, Oak Ridge, Tenn., USA, <a href="https://doi.org/10.3334/CDIAC/ffe.ndp058.2016" target="_blank">https://doi.org/10.3334/CDIAC/ffe.ndp058.2016</a>, 2016a.
</mixed-citation></ref-html>
<ref-html id="bib1.bib2"><label>2</label><mixed-citation>
Andres, R. J., Boden, T. A., and Higdon, D. M.: Gridded uncertainty in fossil fuel carbon dioxide emission maps, a CDIAC example, Atmos. Chem. Phys., 16, 14979–14995, <a href="https://doi.org/10.5194/acp-16-14979-2016" target="_blank">https://doi.org/10.5194/acp-16-14979-2016</a>, 2016b.
</mixed-citation></ref-html>
<ref-html id="bib1.bib3"><label>3</label><mixed-citation>
Boden, T. A., Marland, G., and Andres, R. J.: Global, Regional, and National
Fossil-Fuel CO<sub>2</sub> Emissions. Carbon Dioxide Information Analysis Center,
Oak Ridge National Laboratory, US Department of Energy, Oak Ridge, Tenn., USA, <a href="https://doi.org/10.3334/CDIAC/00001_V2016" target="_blank">https://doi.org/10.3334/CDIAC/00001_V2016</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib4"><label>4</label><mixed-citation>
Brown, D., Brownrigg, R., Haley, M., and Huang, W.:  The NCAR Command Language (NCL) v6.0. 0, UCAR/NCAR Computational
and Information Systems Laboratory, Boulder, CO, <a href="https://doi.org/10.5065/D6WD3XH5" target="_blank">https://doi.org/10.5065/D6WD3XH5</a>, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib5"><label>5</label><mixed-citation>
Dayalu, A.: Exploring the Wide Net of Human Energy Systems: From
Carbon Dioxide Emissions in China to Hydraulic Fracturing Chemicals Usage in
the United States, PhD thesis, Harvard University, Cambridge, MA, 2017.
</mixed-citation></ref-html>
<ref-html id="bib1.bib6"><label>6</label><mixed-citation>
Dayalu, A., Munger, J. W., Wofsy, S. C., Wang, Y., Nehrkorn, T., Zhao, Y., McElroy, M. B., Nielsen, C. P., and Luus, K.: Assessing biotic contributions to CO<sub>2</sub> fluxes in northern China using the Vegetation, Photosynthesis and Respiration Model (VPRM-CHINA) and observations from 2005 to 2009, Biogeosciences, 15, 6713–6729, <a href="https://doi.org/10.5194/bg-15-6713-2018" target="_blank">https://doi.org/10.5194/bg-15-6713-2018</a>, 2018a.
</mixed-citation></ref-html>
<ref-html id="bib1.bib7"><label>7</label><mixed-citation>
Dayalu, A., Munger,  J. W., Wang,  Y., Wofsy,  S. C., Zhao,  Y., Nehrkorn,  T., Nielsen,  C., McElroy,  M. B., and Chang,  R.: Replication Data for: Evaluating China's anthropogenic CO<sub>2</sub> emissions inventories: a northern China case-study using continuous surface observations from 2005–2009, <a href="https://doi.org/10.7910/DVN/OJESO0" target="_blank">https://doi.org/10.7910/DVN/OJESO0</a>, 2018b.
</mixed-citation></ref-html>
<ref-html id="bib1.bib8"><label>8</label><mixed-citation>
European Commission, Joint Research Centre (JRC)/Netherlands Environmental
Assessment Agency (PBL): Emission Database for Global Atmospheric Research
(EDGAR), release EDGARv4.2 FT2010, available at: <a href="http://edgar.jrc.ec.europa.eu" target="_blank"/> (last access: 13 March 2017),
2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib9"><label>9</label><mixed-citation>
Guan, D., Liu, Z., Geng, Y., Lindner, S., and Hubacek, K.: The gigatonne gap
in China's carbon dioxide inventories, Nat. Clim. Change, 2, 672–675,
<a href="https://doi.org/10.1038/nclimate1560" target="_blank">https://doi.org/10.1038/nclimate1560</a>, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib10"><label>10</label><mixed-citation>
Guan, D., Klasen, S., Hubacek, K., Feng, K., Liu, Z., He, K., Geng, Y., and
Zhang Q.: Determinants of stagnating carbon intensity in China, Nat. Clim.
Change, 4, 1017–1023, <a href="https://doi.org/10.1038/nclimate2388" target="_blank">https://doi.org/10.1038/nclimate2388</a>, 2014.
</mixed-citation></ref-html>
<ref-html id="bib1.bib11"><label>11</label><mixed-citation>
Jiang, F., Chen, J., Zhou, L., Ju, W., Zhang, H., Machida, T., Ciais, P., Peters, W., Wang, H., Chen, B., Liu, L., Zhang, C., Matsueda, H., and Sawa, Y.: A comprehensive estimate of recent carbon sinks in China using both top-down and bottom-up approaches, Sci. Rep.-UK, 6, 22130, <a href="https://doi.org/10.1038/srep22130" target="_blank">https://doi.org/10.1038/srep22130</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib12"><label>12</label><mixed-citation>
Karion, A., Sweeney, C., Miller, J. B., Andrews, A. E., Commane, R., Dinardo, S., Henderson, J. M., Lindaas, J., Lin, J. C., Luus, K. A., Newberger, T., Tans, P., Wofsy, S. C., Wolter, S., and Miller, C. E.: Investigating Alaskan methane and carbon dioxide fluxes using measurements from the CARVE tower, Atmos. Chem. Phys., 16, 5383–5398, <a href="https://doi.org/10.5194/acp-16-5383-2016" target="_blank">https://doi.org/10.5194/acp-16-5383-2016</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib13"><label>13</label><mixed-citation>
Kort, E. A., Angevine, W. M., Duren, R., and Miller, C. E.: Surface
observations for monitoring urban fossil fuel CO<sub>2</sub> emissions: Minimum
site location requirements for the Los Angeles megacity, J. Geophys. Res.-Atmos., 118, 1577–1584, <a href="https://doi.org/10.1002/jgrd.50135" target="_blank">https://doi.org/10.1002/jgrd.50135</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib14"><label>14</label><mixed-citation>
Le Quéré, C., Andrew, R. M., Canadell, J. G., Sitch, S., Korsbakken, J. I., Peters, G. P., Manning, A. C., Boden, T. A., Tans, P. P., Houghton, R. A., Keeling, R. F., Alin, S., Andrews, O. D., Anthoni, P., Barbero, L., Bopp, L., Chevallier, F., Chini, L. P., Ciais, P., Currie, K., Delire, C., Doney, S. C., Friedlingstein, P., Gkritzalis, T., Harris, I., Hauck, J., Haverd, V., Hoppema, M., Klein Goldewijk, K., Jain, A. K., Kato, E., Körtzinger, A., Landschützer, P., Lefèvre, N., Lenton, A., Lienert, S., Lombardozzi, D., Melton, J. R., Metzl, N., Millero, F., Monteiro, P. M. S., Munro, D. R., Nabel, J. E. M. S., Nakaoka, S., O'Brien, K., Olsen, A., Omar, A. M., Ono, T., Pierrot, D., Poulter, B., Rödenbeck, C., Salisbury, J., Schuster, U., Schwinger, J., Séférian, R., Skjelvan, I., Stocker, B. D., Sutton, A. J., Takahashi, T., Tian, H., Tilbrook, B., van der Laan-Luijkx, I. T., van der Werf, G. R., Viovy, N., Walker, A. P., Wiltshire, A. J., and Zaehle, S.: Global Carbon Budget 2016, Earth Syst. Sci. Data, 8, 605–649, <a href="https://doi.org/10.5194/essd-8-605-2016" target="_blank">https://doi.org/10.5194/essd-8-605-2016</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib15"><label>15</label><mixed-citation>
Lin, J. C., Gerbig, C., Wofsy, S. C., Andrews, A. E., Daube, B. C., Davis, K. J., and Grainger, C. A.: A near-field tool for simulating the upstream
influence of atmospheric observations: The Stochastic Time-Inverted
Lagrangian Transport (STILT) model, J. Geophys.
Res.-Atmos., 108, 4493, <a href="https://doi.org/10.1029/2002JD003161" target="_blank">https://doi.org/10.1029/2002JD003161</a>, 2003.
</mixed-citation></ref-html>
<ref-html id="bib1.bib16"><label>16</label><mixed-citation>
Liu, Z., Guan, D., Wei, W., Davis, S. J., Ciais, P., Bai, J., Peng, S.,
Zhang, Q., Hubacek, K., Marland, G., Andres, R. J., Crawford-Brown, D., Lin, J., Zhao, H., Hong, C., Boden, T. A., Feng, K., Peters, G. P., Xi, F., Liu, J., Li, Y., Zhao, Y., Zeng, N., and He, K.:  Reduced carbon emission
estimates from fossil fuel combustion and cement production in China, Nature,
524, 335–338, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib17"><label>17</label><mixed-citation>
Mahadevan, P., Wofsy, S. C., Matross, D. M., Xiao, X., Dunn, A. L.,
Lin, J. C., Gerbig, C., Munger, J. W., Chow, V. Y., and Gottlieb, E. W.: A satellite-based biosphere parameterization for net ecosystem CO<sub>2</sub> exchange:
Vegetation Photosynthesis and Respiration Model (VPRM), Global Biogeochem.
Cy., 22, GB2005, <a href="https://doi.org/10.1029/2006GB002735" target="_blank">https://doi.org/10.1029/2006GB002735</a>, 2008.
</mixed-citation></ref-html>
<ref-html id="bib1.bib18"><label>18</label><mixed-citation>
Matross, D. M., Andrews, A., Pathmathevan, M., Gerbig, C., Lin, J. C.,
Wofsy, S. C., Daube, B. C., Gottlieb, E. W., Chow, V. Y., Lee, J. T., Zhao, C. L., Bakwin, P. S., Munger, J. W., and Hollinger, D. Y.: Estimating
regional carbon exchange in New England and Quebec by combining atmospheric,
ground-based and satellite data, Tellus B, 58, 344–358, 2006.
</mixed-citation></ref-html>
<ref-html id="bib1.bib19"><label>19</label><mixed-citation>
McKain, K., Wofsy, S. C., Nehrkorn, T., Eluszkiewicz, Ehleringer, J. R., and
Stephens, B. B.: Assessment of ground-based atmospheric observations for
verification of greenhouse gas emissions from an urban region, P. Natl.
Acad. Sci. USA, 109, 8423–8428, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib20"><label>20</label><mixed-citation>
McKain, K., Down, A., Raciti, S. M., Budney, J., Hutyra, L. R.,
Floerchinger, C., Herndon, S. C., Nehrkorn, T., Zahniser, M. S., and
Jackson, R. B.: Methane emissions from natural gas infrastructure and use in
the urban region of Boston, Massachusetts, P. Natl. Acad. Sci. USA, 112,
1941–1946, 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib21"><label>21</label><mixed-citation>
Miller, S. M., Kort, E. A., Hirsch, A. I., Dlugokencky, E. J., Andrews, A. E.,
Xu, X., Tian, H., Nehrkorn, T. Eluszkiewicz, J., Michalak, A. M., and Wofsy, S. C.: Regional sources of nitrous oxide over the United States: Seasonal
variation and spatial distribution, J. Geophys. Res., 117, D06310,
<a href="https://doi.org/10.1029/2011JD016951" target="_blank">https://doi.org/10.1029/2011JD016951</a>, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib22"><label>22</label><mixed-citation>
Nassar, R., Napier-Linton, L., Gurney, K. R., Andres, R. J., Oda, T., Vogel, F. R., and Deng, F.: Improving the temporal and spatial distribution of
CO<sub>2</sub> emissions from global fossil fuel emission data sets, J. Geophys.
Res.-Atmos., 118, 917–933, <a href="https://doi.org/10.1029/2012JD018196" target="_blank">https://doi.org/10.1029/2012JD018196</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib23"><label>23</label><mixed-citation>
NCEP National Centers for Environmental Prediction/National Weather
Service/NOAA/US Department of Commerce: NCEP FNL Operational Model Global Tropospheric
Analyses, continuing from July 1999, <a href="https://doi.org/10.5065/D6M043C6" target="_blank">https://doi.org/10.5065/D6M043C6</a>,
Research Data Archive at the National Center for Atmospheric Research,
Computational and Information Systems Laboratory, Boulder, Co., updated
daily,  2000.
</mixed-citation></ref-html>
<ref-html id="bib1.bib24"><label>24</label><mixed-citation>
NDRC National Development Reform Commission: Enhanced Actions on Climate
Change: China's Intended Nationally Determined Contributions,  Beijing, China, available at: <a href="https://www4.unfccc.int/sites/ndcstaging/PublishedDocuments/China%20First/China%27s%20First%20NDC%20Submission.pdf&#xA;" target="_blank"/> (last access: 20 March 2020), 2015.
</mixed-citation></ref-html>
<ref-html id="bib1.bib25"><label>25</label><mixed-citation>
Nehrkorn, T., Eluszkiewicz, J., Wofsy, S. C., Lin, J., Gerbig, C., Longo, M.,
and Freitas, S.: Coupled weather research and forecasting–stochastic
time-inverted lagrangian transport (WRF–STILT) model, Meteorol. Atmos.
Phys., 107, 51–64,  <a href="https://doi.org/10.1007/s00703-010-0068-x" target="_blank">https://doi.org/10.1007/s00703-010-0068-x</a>, 2010.
</mixed-citation></ref-html>
<ref-html id="bib1.bib26"><label>26</label><mixed-citation>
Nielsen, C. and Ho, M.: Clearer Skies Over China: Reconciling Air Quality,
Climate, and Economic Goals, MIT Press, ISBN 9780262019880, Cambridge, Mass., USA,
<a href="https://doi.org/10.7551/mitpress/9780262019880.001.0001" target="_blank">https://doi.org/10.7551/mitpress/9780262019880.001.0001</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib27"><label>27</label><mixed-citation>
Niu, Z., Zhou, W., Wu, S., Cheng, P., Lu, X., Xiong, X., Du, H., Fu, Y., and
Wang, G.: Atmospheric Fossil Fuel CO<sub>2</sub> Traced by Δ<sup>14</sup>C in Beijing and
Xiamen, China: Temporal Variations, Inland/Coastal Differences and
Influencing Factors, Environ. Sci. Technol., 50, 5474–5480, <a href="https://doi.org/10.1021/acs.est.5b02591" target="_blank">https://doi.org/10.1021/acs.est.5b02591</a>, 2016
</mixed-citation></ref-html>
<ref-html id="bib1.bib28"><label>28</label><mixed-citation>
Oda, T., Maksyutov, S., and Andres, R. J.: The Open-source Data Inventory for
Anthropogenic CO<sub>2</sub>, version 2016 (ODIAC2016): a global monthly fossil fuel CO<sub>2</sub>
gridded emissions data product for tracer transport simulations and surface
flux inversions, Earth Syst. Sci. Data, 10, 87–107,
<a href="https://doi.org/10.5194/essd-10-87-2018" target="_blank">https://doi.org/10.5194/essd-10-87-2018</a>, 2018.
</mixed-citation></ref-html>
<ref-html id="bib1.bib29"><label>29</label><mixed-citation>
Piao, S., Fang, J., Ciais, P., Peylin, P., Huang, Y., Sitch, S., and Wang, T.: The carbon balance of terrestrial ecosystems in China, Nature,
458, 1009–1013, 2009.
</mixed-citation></ref-html>
<ref-html id="bib1.bib30"><label>30</label><mixed-citation>
Sargent, M., Barrera, Y., Nehrkorn, T., Hutyra, L., Gately, C., Jones, T.,
McKain, K., Sweeney, C., Hegarty, J., Hardiman, B., Wang, J., and Wofsy, S.:
Anthropogenic and biogenic CO<sub>2</sub> fluxes in the Boston urban region, P.
Natl. Acad. Sci. USA, 115, 7491–7496, <a href="https://doi.org/10.1073/pnas.1803715115" target="_blank">https://doi.org/10.1073/pnas.1803715115</a>,
2018.
</mixed-citation></ref-html>
<ref-html id="bib1.bib31"><label>31</label><mixed-citation>
Shan, Y., Liu, J., Liu, Z., Xu, X., Shao, S., Wang, P., and Guan, D.: New
provincial CO<sub>2</sub> emission inventories in China based on apparent energy
consumption data and updated emission factors, Appl. Energ., 184,
742–750, <a href="https://doi.org/10.1016/j.apenergy.2016.03.073" target="_blank">https://doi.org/10.1016/j.apenergy.2016.03.073</a>, 2016.
</mixed-citation></ref-html>
<ref-html id="bib1.bib32"><label>32</label><mixed-citation>
Turnbull, J. C., Tans, P. P., Lehman, S. J., Baker, D., Chung, Y., Gregg, J. S.,
Miller, J. B., Southon, J. R., and Zhao, L.: Atmospheric observations of carbon
monoxide and fossil fuel CO<sub>2</sub> emissions from East Asia, J. Geophys. Res.-Atmos., 116, D24306, <a href="https://doi.org/10.1029/2011JD016691" target="_blank">https://doi.org/10.1029/2011JD016691</a>, 2011.
</mixed-citation></ref-html>
<ref-html id="bib1.bib33"><label>33</label><mixed-citation>
Ummel, K.: CARMA Revisited: An Updated Database of Carbon Dioxide Emissions
from Power Plants Worldwide, CGD Working Paper 304,
Center for Global Development, Washington, DC, available at:
<a href="http://www.cgdev.org/content/publications/detail/1426429" target="_blank"/> (last access: 20 March 2020),
2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib34"><label>34</label><mixed-citation>
US EIA (US Energy Information Administration: Total Carbon Dioxide Emissions from the Consumption of
Energy, available at: <a href="https://www.eia.gov/beta/international/data/browser" target="_blank"/>, last access: 12 January 2017.
</mixed-citation></ref-html>
<ref-html id="bib1.bib35"><label>35</label><mixed-citation>
Wang, R., Tao, S., Ciais, P., Shen, H. Z., Huang, Y., Chen, H., Shen, G. F., Wang, B., Li, W., Zhang, Y. Y., Lu, Y., Zhu, D., Chen, Y. C., Liu, X. P., Wang, W. T., Wang, X. L., Liu, W. X., Li, B. G., and Piao, S. L.: High-resolution mapping of combustion processes and implications for CO<sub>2</sub> emissions, Atmos. Chem. Phys., 13, 5189–5203, <a href="https://doi.org/10.5194/acp-13-5189-2013" target="_blank">https://doi.org/10.5194/acp-13-5189-2013</a>, 2013.
</mixed-citation></ref-html>
<ref-html id="bib1.bib36"><label>36</label><mixed-citation>
Wang, X., Wang, Y. X., Hao, J. M., Kondo, Y., Irwin, M., Munger, J. W., and
Zhao, Y. J.: Top-down estimate of China's black carbon emissions using surface
observations: Sensitivity to observation representativeness and transport
model error, J. Geophys. Res.-Atmos., 118, 5781–5795, <a href="https://doi.org/10.1002/jgrd.50397" target="_blank">https://doi.org/10.1002/jgrd.50397</a>. 2013.

</mixed-citation></ref-html>
<ref-html id="bib1.bib37"><label>37</label><mixed-citation>
Wang, Y., Munger, J. W., Xu, S., McElroy, M. B., Hao, J., Nielsen, C. P., and Ma, H.: CO<sub>2</sub> and its correlation with CO at a rural site near Beijing: implications for combustion efficiency in China, Atmos. Chem. Phys., 10, 8881–8897, <a href="https://doi.org/10.5194/acp-10-8881-2010" target="_blank">https://doi.org/10.5194/acp-10-8881-2010</a>, 2010.
</mixed-citation></ref-html>
<ref-html id="bib1.bib38"><label>38</label><mixed-citation>
Wang, Y., Wang, X., Kondo, Y., Kajino, M., Munger, J. W., and Hao, J.: Black
carbon and its correlation with trace gases at a rural site in Beijing:
Top-down constraints from ambient measurements on bottom-up emissions,
J. Geophys. Res.-Atmos., 116, D24304, <a href="https://doi.org/10.1029/2011jd016575" target="_blank">https://doi.org/10.1029/2011jd016575</a>, 2011.
</mixed-citation></ref-html>
<ref-html id="bib1.bib39"><label>39</label><mixed-citation>
World Bank:  CO<sub>2</sub> emissions (kg per PPP $ of GDP), available at:
<a href="https://data.worldbank.org/indicator/EN.ATM.CO2E.PP.GD?locations=CN" target="_blank"/>,
last access: 12 May 2017.
</mixed-citation></ref-html>
<ref-html id="bib1.bib40"><label>40</label><mixed-citation>
Zhao, Y., Nielsen, C. P., and McElroy, M.: China's CO<sub>2</sub> emissions
estimated from the bottom up: Recent trends, spatial distributions, and
quantification of uncertainties, Atmos. Environ., 59, 214–223, 2012.
</mixed-citation></ref-html>
<ref-html id="bib1.bib41"><label>41</label><mixed-citation>
Zhao, Y., Zhang, J., and Nielsen, C. P.: The effects of recent control policies on trends in emissions of anthropogenic atmospheric pollutants and CO<sub>2</sub> in China, Atmos. Chem. Phys., 13, 487–508, <a href="https://doi.org/10.5194/acp-13-487-2013" target="_blank">https://doi.org/10.5194/acp-13-487-2013</a>, 2013.
</mixed-citation></ref-html>--></article>
