of 6
New constraints on Northern Hemisphere growing season net flux
Z. Yang,
1
R. A. Washenfelder,
2,3
G. Keppel-Aleks,
2
N. Y. Krakauer,
1,4
J. T. Randerson,
5
P. P. Tans,
6
C. Sweeney,
7
and P. O. Wennberg
1,2
Received 5 March 2007; revised 27 April 2007; accepted 1 May 2007; published 23 June 2007.
[
1
] Observations of the column-averaged dry molar mixing
ratio of CO
2
above both Park Falls, Wisconsin and Kitt Peak,
Arizona, together with partial columns derived from aircraft
profiles over Eurasia and North America are used to estimate
the seasonal integral of net ecosystem exchange (NEE)
between the atmosphere and the terrestrial biosphere in the
Northern Hemisphere. We find that NEE is

25% larger than
predicted by the Carnegie Ames Stanford Approach
(CASA) model. We show that the estimates of NEE
may have been biased low by too weak vertical mixing in
the transport models used to infer seasonal changes in
Northern Hemisphere CO
2
mass from the surface
measurements of CO
2
mixing ratio.
Citation:
Yang, Z.,
R. A. Washenfelder, G. Keppel-Aleks, N. Y. Krakauer, J. T.
Randerson, P. P. Tans, C. Sweeney, and P. O. Wennberg (2007),
New constraints on Northern Hemisphere growing season net flux,
Geophys. Res. Lett.
,
34
, L12807, doi:10.1029/2007GL029742.
1. Introduction
[
2
] Forecasting CO
2
levels in the atmosphere is needed to
predict future climate. Accurate forecasts require an im-
proved understanding of carbon sources and sinks [
Inter-
governmental Panel on Climate Change
, 2001]. During the
1990s, fossil fuel combustion and cement production added
approximately 6 Pg C yr

1
to the atmosphere. These fluxes
are well constrained spatially and temporally [
Andres et al.
,
1996]. From the observed atmospheric increase and the
known anthropogenic emissions, the combined ocean and
terrestrial biosphere carbon sinks must have been close to 3
Pg C yr

1
[
Intergovernmental Panel on Climate Change
,
2001].
[
3
] To estimate the spatial and temporal distribution of
these carbon sinks, inverse methods have been used to infer
carbon fluxes from geographically sparse observations of
atmospheric CO
2
mixing ratio, typically measured at the
surface [e.g.,
Tans et al.
, 1990]. In these methods, surface
fluxes are scaled within the framework of an atmospheric
transport model to minimize the difference between the
observed and simulated spatial and temporal gradients of
atmospheric CO
2
mixing ratio [
Enting et al.
, 1995;
Kaminski
et al.
, 1999;
Rayner et al.
, 1999;
Bousquet et al.
, 2000;
Krakauer et al.
, 2004;
Baker et al.
, 2006]. Estimates of both
net ecosystem exchange (NEE) and the geographical distri-
bution of fossil fuel carbon sinks vary substantially due in
large part to errors in the atmospheric transport models used
in these inversions [e.g.,
Gurney et al.
, 2004]. This is quite
understandable; estimation of fluxes (i.e., mass m

2
s

1
)on
large geographical scales requires knowledge of temporal
and spatial gradients in CO
2
column abundance (i.e., mass
m

2
) in the atmosphere. These gradients in CO
2
column can
be inferred from gradients in the observed mixing ratio at
the surface only if the vertical structure of atmospheric CO
2
is well known. Proper simulation of the vertical structure
requires accurate simulation of the exchange between the
planetary boundary layer (PBL) and the free troposphere: a
difficult requirement and an area of active research in the
atmospheric dynamics community.
[
4
] In this study, we use newly available observations of
the column and vertical profile dry air CO
2
molar mixing
ratios above eight sites (Table 1) to estimate the seasonally-
varying carbon flux (NEE) in the northern hemisphere.
Because these observations are of the column or partial
column abundance, they come close to directly representing
a measure of atmospheric CO
2
mass per unit area. As
a result, our estimate of NEE are less sensitive to errors in
the vertical transport than estimates based solely on surface
mixing ratio observations. Our analysis suggests that the
seasonally-varying fluxes are substantially larger than the
NEE fluxes from the CASA model used in the TransCom 3
studies. We further show, using vertically resolved observa-
tions of CO
2
obtained at several sites in Eurasia and North
America, that the TransCom models underestimate the
seasonally-varying fluxes because they underestimate the
efficiency of CO
2
mixing throughout the free troposphere.
2. Measurements and Models
[
5
] Measurements of column-averaged dry mixing ratio
of CO
2
were obtained at Park Falls, Wisconsin beginning in
2004. Using an automated solar observatory, direct solar
spectra were acquired continuously during clear-sky, day-
time conditions. These spectra were used to determine
vertically integrated CO
2
with high precision (0.1%) and
accuracy (0.3%) [
Washenfelder et al.
, 2006]. The 337 days
of measurements were taken during May 2004 to November
2006 and have been averaged daily. We also included
similar but much infrequent (only 96 days during the two
periods: Jan 1979 to Dec 1985 and Mar 1989 to Mar 1995)
column measurements obtained at the Kitt Peak solar obser-
vatory, Arizona [
Yang et al.
, 2002]. In addition to the ground-
GEOPHYSICAL RESEARCH LETTERS, VOL. 34, L12807, doi:10.1029/2007GL029742, 2007
1
Division of Geological and Planetary Sciences, California Institute of
Technology, Pasadena, California, USA.
2
Division of Engineering and Applied Science, California Institute of
Technology, Pasadena, California, USA.
3
Now at Chemical Sciences Division, Earth System Research
Laboratory, NOAA, Boulder, Colorado, USA.
4
Now at Department of Earth and Planetary Science, University of
California, Berkeley, California, USA.
5
Department of Earth System Science, University of California, Irvine,
California, USA.
6
Earth System Research Laboratory, NOAA, Boulder, Colorado, USA.
7
Cooperative Institute for Research in Environmental Sciences,
University of Colorado, Boulder, Colorado, USA.
Copyright 2007 by the American Geophysical Union.
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0
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4
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0
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L12807
1of6
based total columns, multi-level aircraft CO
2
measurements
were available at six sites in North America and Eurasia
during 2003–2004 (Table 1). Discrete CO
2
samples were
acquired biweekly or monthly during aircraft profiles up to
7500 m above the surface [e.g.,
Levin et al.
, 2002]. In our
analysis, we used the interpolations of these measurements at
fixed temporal (48 per year) and spatial (every 500 m in
altitude) intervals [
GLOBALVIEW-CO
2
, 2006].
[
6
] To compare with the observations, we used the twelve
TransCom 3 experiment models that differ in spatial reso-
lution, advection scheme, driving winds, and sub-grid scale
parameterizations [
Gurney et al.
, 2003]. Monthly terrestrial
biosphere exchange (1
°

1
°
) was derived from the Carne-
gie-Ames-Stanford Approach (CASA) terrestrial biosphere
model [
Randerson et al.
, 1997], and is annually balanced at
each grid cell.
3. Methods
[
7
] In our analysis, we compare the observed amplitude
and phase of the atmospheric CO
2
seasonal cycles to
simulations obtained from propagating seasonal surface
fluxes from a terrestrial biosphere model (CASA) with
annually-balanced fluxes through the twelve different trans-
port models. Since the same fluxes are used, differences in
the simulated atmospheric CO
2
seasonal cycles at different
altitudes and locations result only from the differences in
transport in the models. To quantify the differences between
the observations and the simulations, we use a simple least
squares fit, assuming the observed seasonal cycle
S
(t) can
be expressed as a function of the simulated CASA bio-
sphere model response
S
0
(t), adjusted by scale factor
A
, time
delay
T
, and offset
B
:
S
t
ðÞ¼
A

S
0
t

T
ðÞþ
B
ð
1
Þ
[
8
] Focusing on the shape of seasonal cycle, we report
A
and
T
but not offset
B
. The
A
and
T
parameters can also be
thought of as two spatially uniform adjustments to all
CASA surface fluxes because of the linear relationship
between these fluxes and
S
(t). Besides the simulations from
the twelve models, the mean of all these models’ simula-
tions is considered as our ‘‘best’’ estimate and included in
the comparison. The fitting rms (
s
) for the all-model mean
simulation is reported to measure the goodness of the fit,
and to derive a weighted mean CASA scale factor (but not
time delay) for
n
different sites:

A
¼
P
n
i
¼
1
A
i
=
s
2
i
P
n
i
¼
1
1
=
s
2
i
ð
2
Þ
[
9
] To compare the observations with the neutral bio-
sphere simulations, the measurements were detrended and
offset by the annual mean value. The interannual trend for
the Park Falls column CO
2
was empirically determined as
1.80 ppm yr

1
during 2004 to 2006. For Kitt Peak, the
trends were 1.41 ppm yr

1
during 1979 to 1985 and
0.83 ppm yr

1
during 1989 to 1995. For the temporally
evenly spaced GlobalView assimilations, their seasonal
cycles were directly decomposed using the empirical mode
decomposition method [
Huang et al.
, 1998] and folded into
one year.
4. Results and Discussion
[
10
] The comparison between the Park Falls CO
2
season-
al cycle of column-averaged observation and the TransCom
simulations is shown in Figure 1. The observed seasonal
CO
2
cycle amplitude is larger than any model simulation. A
best fit was obtained by increasing the CASA fluxes by
34%. Models also underestimated the CO
2
seasonal cycle at
Kitt Peak and at all the other six aircraft sites. The average
difference across all the column and partial column sites
was 28% (Table 1). Because these vertically-integrated
observations sample a substantial fraction of the northern
hemisphere landmass, they provide a measure of CO
2
variations that is not highly sensitive to error in the transport
fields. As a group, the seasonal cycle in column CO
2
is most
sensitive to the seasonal fluxes themselves. This is sup-
ported by the relatively small variation in the model
simulations of the columns illustrated for Park Falls in
Table 1.
Column and Profile Observation Sites and the CO
2
Seasonal Cycle Amplitude Comparison With Model Simulations
Site Name (Code)
Location
Altitude Range
Above
Surface, m
Mean Scale
Factor
A
of the 12
Models
a,b
Phase Shift
T
of 12
Models,
days
Scale Factor
A
for the
Mean Response
of the 12
Models
RMS in Fitting
the Mean Response
of the 12
Models, ppm
Poker Flats, AK (PFA)
65.07
°
N, 147.29
°
W 1500–7500 1.20 ± 0.11

16.8 ± 4.5
1.21
0.71
Zotino, Russia (ZOT)
60.75
°
N, 89.38
°
E
500–3500 1.44 ± 0.21

18.4 ± 2.8
1.42
1.70
Estevan Point, Canada (ESP)
49.38
°
N, 126.55
°
W 500–5500 1.20 ± 0.12

16.0 ± 3.2
1.20
0.54
Orleans, France (ORL)
47.80
°
N, 2.50
°
E
500–3500 1.39 ± 0.18

19.6 ± 3.1
1.38
0.43
Park Falls, WI (LEF)
45.93
°
N, 90.27
°
W Total column 1.34 ± 0.14

7.3 ± 4.0
1.34
0.43
Harvard Forest, MA (HFM)
42.54
°
N, 72.17
°
W
500–7500 1.38 ± 0.09

16.0 ± 2.7
1.38
0.67
Carr, CO (CAR)
40.90
°
N, 104.80
°
W 1500–6500 1.20 ± 0.11

7.6 ± 7.3
1.21
0.56
Kitt Peak, AZ
c
(KTP)
31.90
°
N, 111.60
°
W Total column 1.11 ± 0.07 15.3 ± 4.6
1.12
0.56
Mean
1.28

14.5 ± 5.0
d
1.28
0.70
Mean of 35 surface sites
e
in 30
°
N

70
°
N
1.12

11.9 ± 9.8
1.11
1.07
a
For LEF and KTP, total CO
2
columns were simulated for the comparison. For the aircraft sites, only partial columns with measurements were simulated.
The scale factor
A
and phase shift
T
here are described by equation (1).
b
The names of the models are CSU.gurney, GISS.prather, GISS.prather2, GISS.prather3, JMA-CDTM.maki, MATCH.bruhwiler, MATCH.chen,
MATCH.law, RPN.yuen, SKYHI.fan, TM3.heimann, GCTM.baker. For more detail refer to TransCom website (http://www.purdue.edu/transcom/) and
Gurney et al.
[2003].
c
The Kitt Peak observations were taken from Jan 1979 to Mar 1995, for more detail refer to
Yang et al.
[2002].
d
Excluding Kitt Peak due to different observation time period.
e
These surface sites are part of the
Globalview-CO
2
[2006] network, for a detailed list see auxiliary material.
L12807
YANG ET AL.: LARGER NORTH HEMISPHERE NET ECOSYSTEM EXCHANGE
L12807
2of6
Figure 1 and for the other sites in the accompanying
auxiliary material
1
. Our column-based optimization implies
that the true growing season net flux (GSNF) in the northern
hemisphere is approximately 28% greater than that pre-
dicted by CASA. North of 30
°
N, this corresponds to a
GSNF of 7.9 Pg C/yr.
[
11
] The results shown here are not sensitive to the
seasonally-varying fossil fuel fluxes. We repeated our
analysis to investigate the impact of seasonally-varying
fossil fuel emissions (in 1995) estimated by A. L. Brenkert
(Carbon dioxide emission estimates from fossil-fuel burn-
ing, hydraulic cement production, and gas flaring for 1995
on a one degree grid cell basis, 1998 (data available at http://
cdiac.esd.ornl.gov/epubs/ndp/ndp058a/ndp058a.html)) on
our estimate of the seasonal cycle of carbon dioxide due to
terrestrial processes. Including this estimate of fossil fuel
emissions increases our estimate of the terrestrial fluxes
obtained from the column data by

1% in average and
decreases the estimate obtained from the surface observations
by a similar amount (see auxiliary material).
[
12
] The NEE from CASA was derived from 1990
satellite observations, and so the observed 0.66% yr

1
increase rate of CO
2
seasonal-signal amplitude between
1981 to 1995 [
Randerson et al.
, 1997] may explain some,
but clearly not all, of the differences between the observa-
tions and simulations of the CO
2
seasonal cycle amplitude.
In addition, the phase analysis of CO
2
seasonal cycles
shown in Table 1 shows that for all sites except Kitt Peak,
CASA fluxes needed to be shifted earlier by one to three
weeks, which may, in part, be explained by advances in the
timing of spring thaw since 1988 [
Smith et al.
, 2004]. More
generally, although changes in the seasonality of terrestrial
fluxes and the annual mean flux are probably linked by
means of long-term trends in photosynthesis and respiration,
this relationship is complex and not necessarily predictable
without more information about the underlying drivers
[
Randerson et al.
, 1999]. For example, if the 2.3 Pg C/yr
Northern Hemisphere terrestrial sink inferred by
Gurney et
al.
[2002] were caused by long-term gains in carbon during
spring or fall, it might cause the seasonal cycle of atmo-
spheric carbon dioxide to decrease, whereas gains during
mid-summer may have the opposite effect. Further, rela-
tively large carbon sinks may be sustained by very small
long-term increases in net primary production (much less
than 1% yr

1
)[
Friedlingstein et al.
, 1995] that would have
a small influence on the observed season cycle of CO
2
.
[
13
] In contrast to the column results, comparison of the
simulations of the seasonal cycle with CO
2
observations
obtained at the surface (GLOBALVIEW-CO
2
flasks)
between 30
°
Nto70
°
N shows a much smaller under-
estimation of seasonal cycle (

12%, Table 1) and a smaller
phase delay (
T
surface
=

11.9 days;
T
column
=

14.5 days).
Both the amplitude and phase differences between the
estimates from surface and column observations suggest
that the TransCom models as a group do not mix the surface
fluxes into the free troposphere quickly enough.
[
14
] The vertical propagation of the seasonal cycle of
CO
2
from its source at the surface into the interior of the
atmosphere is sensitive to the efficiency of vertical ex-
change. To investigate the accuracy of the TRANSCOM
model simulations of this propagation, we analyzed the CO
2
vertical profiles at the six sites sampled by the aircraft.
Directly comparing the simulations and observations for
these sites using the same analysis method as described
above was, however, hampered by large differences in the
shape of the CO
2
seasonal cycle at some sites (e.g., ZOT in
Figure 2). (The results of such an analysis are shown in the
online supplement
1
; the retrieved CASA scale factors
increase with altitude, but the increase is not statistically
significant.) To minimize the impact of this mismatch, we
analyzed the simulations (using the a priori CASA fluxes)
and the atmospheric observation separately. At each site, we
defined a reference height (3500 m) and fit the seasonal
cycles
S
H
(t) at all other heights (H) in both the observations
and simulations by:
S
H
t
ðÞ¼
A
H

S
3500
t

T
H
ðÞþ
B
ð
3
Þ
Figure 1.
(a) Atmospheric column-average CO
2
mole
fractions at Park Falls for May 2004–March 2006. (b) The
monthly mean of observations (closed circles) compared
with the TransCom simulations (grey shade shows range of
12-model predictions; thin solid line represents average).
Each of the 12 models underpredicts the seasonal cycle
observed in the column measurements. The best match to the
observations is achieved by scale the model-mean simula-
tions by 1.34 and shift them 7 days earlier (thick solid line).
1
Auxiliary material data sets are available at ftp://ftp.agu.org/apend/gl/
2007gl029742. Other auxiliary material files are in the HTML.
L12807
YANG ET AL.: LARGER NORTH HEMISPHERE NET ECOSYSTEM EXCHANGE
L12807
3of6
where
T
H
represents the time delay,
A
H
is the scaled
amplitude and
B
is a seasonally-invariant offset. The
comparison for each site is shown in Figure 2 and the
retrieved values of
A
H
and
T
H
are listed in Table 2. In
the model simulations, the scale factors monotonically
decrease with altitude at all sites, while the time delays
monotonically increase. In contrast, in the observations at or
above 2500 m, all sites except ESP showed smaller
decreases or even increases in the amplitude scale factor
with altitude as well as shorter delay, and even advance (at
PFA) in the seasonal cycle phase. For levels below 2500 m,
the observations showed mixed trends from site to site,
again possibly influenced by strong PBL variation. The
observation-model differences above 2500 m strongly
suggest that the atmospheric vertical and/or meridional
mixing within the free troposphere is faster than the
TransCom simulations.
5. Summary and Implications
[
15
] Comparison of the column-averaged CO
2
dry volume
mixing ratio measurements and the TransCom models
implies that GSNF north of 30
°
Nis

7.9 Pg C/yr, approx-
imately 28% larger than that predicted by CASA. Using
multi-level observed CO
2
from the Northern hemisphere to
diagnose the model performance at different altitudes, we
identify substantial underestimation of free troposphere
vertical mixing rates by TransCom models. While the
mixing between the PBL and the free troposphere has
been a major focus of carbon flux inversion experiments
(i.e. TransCom), this analysis suggests that equally large
Figure 2.
Comparison of the CO
2
seasonal cycles at different levels, for both (left) the aircraft observations and (right)
the TransCom 12-model mean simulation. Each altitude level is represented by a different line and each row represents
one site respectively. The range of model simulations for 3500 meters altitude is also shown in the left panel as the
shaded area.
L12807
YANG ET AL.: LARGER NORTH HEMISPHERE NET ECOSYSTEM EXCHANGE
L12807
4of6
errors exist in the rate of vertical mixing throughout the
free troposphere.
[
16
] The weak vertical exchange of the TransCom models
will have impacts beyond the estimation of seasonal CO
2
exchange between the biosphere and atmosphere.
Gurney et
al.
[2004] have shown, for example, that the inferred uptake
of fossil fuel carbon by land in the Northern Hemisphere by
the various TransCom models (from 0.0 to 4.0 Pg C/yr
depending on which transport model is used) is correlated
with their estimate of the CO
2
seasonal cycle produced by
the biosphere fluxes. Gurney et al. suggest that this corre-
lation is consistent with errors in parameterization of the
seasonal mixing efficiency between the planetary boundary
layer (PBL) and the free troposphere (FT), which co-varies
in time with the surface carbon exchange direction and
strength [
Denning et al.
, 1995]. Our finding suggests that as
a group, the TransCom models may have too little vertical
mixing in the free troposphere and so may overestimate the
size of the Northern Hemisphere land sink. The validity of
this inference, however, depends in part on the how the
transport errors vary seasonally, something this study has
not addressed.
[
17
] The analysis described in this letter illustrates the
utility of having information about the vertical distribution
of CO
2
from aircraft. In addition, the total column measure-
ments allow a more continuous record of CO
2
mass. The
Total Carbon Column Observing Network (TCCON) is
being established to expand the number of sites where
CO
2
columns are measured (data available at http://
www.tccon.caltech.edu). TCCON will include a number
of sites in both the Northern and Southern Hemispheres.
These observations should provide an improved measure of
the gradient in CO
2
mass between two hemispheres. Based
on the findings of this study, we expect that the N–S
gradient will be larger than predicted by the TransCom
inversions tied to surface observations.
[
18
]
Acknowledgments.
We thank the TransCom 3 modeling com-
munity (K. Gurney, M. Prather, T. Maki, L. Bruhwiler, Y. Chen, R. Law,
C. Yuen, S. Fan, M. Heimann, and D. Baker) for making the results of
their simulations publicly available. This work was supported by a NASA
grant NNG05GD07G. N. Y. Krakauer was supported by Graduate Fellow-
ships from both NASA Earth and Space Science and the Betty and
Gordon Moore Foundation.
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Table 2.
Optimal Values of Scale Factor,
A
H
, and Time Delay in Days,
T
H
, Applied to 3500-m-Level Seasonal CO
2
Cycle for Best
Matching the Other Levels (Equation (3))
a
Altitude
Optimal Values for Scale Factor
A
H
PFA
ZOT
ESP
ORL
HFM
CAR
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
7500 m
0.88
0.80
0.78
0.74
6500 m
0.93
0.85
0.87
0.78
1.05
0.90
5500 m
0.89
0.90
0.74
0.91
0.83
0.84
1.00
0.94
4500 m
0.92
0.95
0.89
0.95
0.85
0.91
1.05
0.98
3500 m
1.00
1.00
1.00
1.00
1.00
1.00
1.00
1.00
1.00
1.00
1.00
1.00
2500 m
1.03
1.12
1.18
1.20
1.07
1.07
1.03
1.06
1.25
1.23
0.98
1.12
1500 m
1.33
1.30
1.32
1.51
1.24
1.16
1.41
1.12
1.67
1.57
0.96
1.26
Optimal Values for Time Delay
T
H
, days
Altitude
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
Obs.
Mod.
7500 m

2.0
7.0
13.0
13.0
6500 m

4.0
6.0
11.0
10.0
3.0
12.0
5500 m

1.0
4.0
8.0
1.0
10.0
8.0

2.0
10.0
4500 m
0.0
2.0

3.0
1.0
6.0
4.0

4.0
8.0
3500 m
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
0.0
2500 m

5.0

4.0

4.0

5.0

4.0

1.0

5.0

3.0

6.0

6.0

4.0

8.0
1500 m

7.0

10.0

10.0

10.0

4.0

2.0

12.0

7.0

21.0

13.0

4.0

16.0
a
For each site, the left column is for the observations and the right column is for the 12-model mean simulations.
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G. Keppel-Aleks and P. O. Wennberg, Division of Engineering and
Applied Science, California Institute of Technology, Pasadena, CA 91125,
USA. (wennberg@caltech.edu)
N. Y. Krakauer, Department of Earth and Planetary Science, University of
California, Berkeley, CA 94720, USA. (niryk@berkeley.edu)
J. T. Randerson, Department of Earth System Science, University of
California, Irvine, CA 92697, USA. (jranders@uci.edu)
C. Sweeney, Cooperative Institute for Research in Environmental Sciences,
University of Colorado, Boulder, CO 80309, USA. (colm.sweeney@noaa.
gov)
P. P. Tans, Earth System Research Laboratory, National Oceanic and
Atmospheric Administration, Boulder, CO 80305, USA. (pieter.tans@
noaa.gov)
R. A. Washenfelder, Chemical Sciences Division, Earth System Research
Laboratory, NOAA, Boulder, CO 80305, USA. (rebecca.washenfelder@
noaa.gov)
Z. Yang, Division of Geological and Planetary Sciences, California
Institute of Technology, Pasadena, CA 91125, USA. (yangzh@caltech.edu)
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