John B. Miller

Dr. John B. Miller

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Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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27 November 2007 in Proceedings of the National Academy of Sciences
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Journal Article
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WPWouter Peters
Wouter Peters
AJAndrew R. Jacobson
Andrew R. Jacobson
CSColm Sweeney
Colm Sweeney
AAArlyn E. Andrews
Arlyn E. Andrews
TCThomas J. Conway
Thomas J. Conway
PTPieter P. Tans
Pieter P. Tans
We present an estimate of net CO 2 exchange between the terrestrial biosphere and the atmosphere across North America for every week in the period 2000 through 2005. This estimate is derived from a set of 28,000 CO 2 mole fraction observations in the global atmosphere that are fed into a state-of-the-art data assimilation system for CO 2 called CarbonTracker. By design, the surface fluxes produced in CarbonTracker are consistent with the recent history of CO 2 in the atmosphere and provide constraints on the net carbon flux independent from national inventories derived from accounting efforts. We find the North American terrestrial biosphere to have absorbed −0.65 PgC/yr (1 petagram = 10 15 g; negative signs are used for carbon sinks) averaged over the period studied, partly offsetting the estimated 1.85 PgC/yr release by fossil fuel burning and cement manufacturing. Uncertainty on this estimate is derived from a set of sensitivity experiments and places the sink within a range of −0.4 to −1.0 PgC/yr. The estimated sink is located mainly in the deciduous forests along the East Coast (32%) and the boreal coniferous forests (22%). Terrestrial uptake fell to −0.32 PgC/yr during the large-scale drought of 2002, suggesting sensitivity of the contemporary carbon sinks to climate extremes. CarbonTracker results are in excellent agreement with a wide collection of carbon inventories that form the basis of the first North American State of the Carbon Cycle Report (SOCCR), to be released in 2007. All CarbonTracker results are freely available at http://carbontracker.noaa.gov .

1 September 2006 in Nature
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Journal Article
Closed access
PBP. Bousquet
P. Bousquet
PCP. Ciais
P. Ciais
JMJohn B. Miller
John B. Miller
EDE. J. Dlugokencky
E. J. Dlugokencky
DHD. A. Hauglustaine
D. A. Hauglustaine
JWJ. White
J. White

13 February 2018 in Nature Communications
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Journal Article
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Luiz AragaoLuiz Aragao
Luiz Aragao
LALiana O. Anderson
Liana O. Anderson
MFMarisa Fonseca
Marisa Fonseca
TRThais M. Rosan
Thais M. Rosan
LVLaura B. Vedovato
Laura B. Vedovato
SSSassan Saatchi
Sassan Saatchi
Tropical carbon emissions are largely derived from direct forest clearing processes. Yet, emissions from drought-induced forest fires are, usually, not included in national-level carbon emission inventories. Here we examine Brazilian Amazon drought impacts on fire incidence and associated forest fire carbon emissions over the period 2003–2015. We show that despite a 76% decline in deforestation rates over the past 13 years, fire incidence increased by 36% during the 2015 drought compared to the preceding 12 years. The 2015 drought had the largest ever ratio of active fire counts to deforestation, with active fires occurring over an area of 799,293 km2. Gross emissions from forest fires (989 ± 504 Tg CO2 year−1) alone are more than half as great as those from old-growth forest deforestation during drought years. We conclude that carbon emission inventories intended for accounting and developing policies need to take account of substantial forest fire emissions not associated to the deforestation process.

1 August 2012 in Nature
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Journal Article
Closed access
ABA. P. Ballantyne
A. P. Ballantyne
CACaroline Alden
Caroline Alden
JMJohn B. Miller
John B. Miller
PTP. P. Tans
P. P. Tans
JWJ. W. C. White
J. W. C. White

5 October 2016 in Nature
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Journal Article
Closed access
SSStefan Schwietzke
Stefan Schwietzke
OSOwen A. Sherwood
Owen A. Sherwood
LBLori M. P. Bruhwiler
Lori M. P. Bruhwiler
JMJohn B. Miller
John B. Miller
GEGiuseppe Etiope
Giuseppe Etiope
PTPieter P. Tans
Pieter P. Tans

17 September 2009 in Geophysical Research Letters
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Journal Article
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EDE. J. Dlugokencky
E. J. Dlugokencky
LBL. Bruhwiler
L. Bruhwiler
JWJ. W. C. White
J. W. C. White
LEL. K. Emmons
L. K. Emmons
PNP. C. Novelli
P. C. Novelli
LGLuciana V. Gatti
Luciana V. Gatti
Measurements of atmospheric CH4 from air samples collected weekly at 46 remote surface sites show that, after a decade of near‐zero growth, globally averaged atmospheric methane increased during 2007 and 2008. During 2007, CH4 increased by 8.3 ± 0.6 ppb. CH4 mole fractions averaged over polar northern latitudes and the Southern Hemisphere increased more than other zonally averaged regions. In 2008, globally averaged CH4 increased by 4.4 ± 0.6 ppb; the largest increase was in the tropics, while polar northern latitudes did not increase. Satellite and in situ CO observations suggest only a minor contribution to increased CH4 from biomass burning. The most likely drivers of the CH4 anomalies observed during 2007 and 2008 are anomalously high temperatures in the Arctic and greater than average precipitation in the tropics. Near‐zero CH4 growth in the Arctic during 2008 suggests we have not yet activated strong climate feedbacks from permafrost and CH4 hydrates.