INTRODUCTION The influence of El Niño on climate is accompanied by large changes to the carbon cycle, and El Niño–induced variability in the carbon cycle has been attributed mainly to the tropical continents. However, owing to a dearth of observations in the tropics, tropical carbon fluxes are poorly quantified, and considerable debate exists over the dominant mechanisms (e.g., plant growth, respiration, fire) and regions (e.g., humid versus semiarid tropics) on the net carbon balance. RATIONALE The launch of the Orbiting Carbon Observatory-2 (OCO-2) shortly before the 2015–2016 El Niño, the second strongest since the 1950s, has provided an opportunity to understand how tropical land carbon fluxes respond to the warm and dry climate characteristics of El Niño conditions. The El Niño events may also provide a natural experiment to study the response of tropical land carbon fluxes to future climate changes, because anomalously warm and dry tropical environments typical of El Niño are expected to be more frequent under most emission scenarios. RESULTS The tropical regions of three continents (South America, Asia, and Africa) had heterogeneous responses to the 2015–2016 El Niño, in terms of both climate drivers and the carbon cycle. The annual mean precipitation over tropical South America and tropical Asia was lower by 3.0σ and 2.8σ, respectively, in 2015 relative to the 2011 La Niña year. Tropical Africa, on the other hand, had near equal precipitation and the same number of dry months between 2015 and 2011; however, surface temperatures were higher by 1.6σ, dominated by the positive anomaly over its eastern and southern regions. In response to the warmer and drier climate anomaly in 2015, the pantropical biosphere released 2.5 ± 0.34 gigatons more carbon into the atmosphere than in 2011, which accounts for 83.3% of the global total 3.0–gigatons of carbon (gigatons C) net biosphere flux differences and 92.6% of the atmospheric CO 2 growth-rate differences between 2015 and 2011. It indicates that the tropical land biosphere flux anomaly was the driver of the highest atmospheric CO 2 growth rate in 2015. The three tropical continents had an approximately even contribution to the pantropical net carbon flux anomaly in 2015, but had diverse dominant processes: gross primary production (GPP) reduced carbon uptake (0.9 ± 0.96 gigatons C) in tropical South America, fire increased carbon release (0.4 ± 0.08 gigatons C) in tropical Asia, and respiration increased carbon release (0.6 ± 1.01 gigatons C) in Africa. We found that most of the excess carbon release in 2015 was associated with either extremely low precipitation or high temperatures, or both. CONCLUSION Our results indicate that the global El Niño effect is a superposition of regionally specific effects. The heterogeneous climate forcing and carbon response over the three tropical continents to the 2015–2016 El Niño challenges previous studies that suggested that a single dominant process determines carbon cycle interannual variability, which could also be due to previous disturbance and soil and vegetation structure. The similarity between the 2015 tropical climate anomaly and the projected climate changes imply that the role of the tropical land as a buffer for fossil fuel emissions may be reduced in the future. The heterogeneous response may reflect differences in temperature and rainfall anomalies, but intrinsic differences in vegetation species, soils, and prior disturbance may contribute as well. A synergistic use of multiple satellite observations and a long time series of spatially resolved fluxes derived from sustained satellite observations will enable tests of these hypotheses, allow for a more process-based understanding, and, ultimately, aid improved carbon-climate model projections. Diverse climate driver anomalies and carbon cycle responses to the 2015–2016 El Niño over the three tropical continents. Schematic of climate anomaly patterns over the three tropical continents and the anomalies of the net carbon flux and its dominant constituent flux (i.e., GPP, respiration, and fire) relative to the 2011 La Niña during the 2015–2016 El Niño. GtC, gigatons C.

We estimate methane emissions from North America with high spatial resolution by inversion of Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) satellite observations using the Goddard Earth Observing System Chemistry (GEOS-Chem) chemical transport model and its adjoint. The inversion focuses on summer 2004 when data from the Intercontinental Chemical Transport Experiment-North America (INTEX-A) aircraft campaign over the eastern U.S. are available to validate the SCIAMACHY retrievals and evaluate the inversion. From the INTEX-A data we identify and correct a water vapor-dependent bias in the SCIAMACHY data. We conduct an initial inversion of emissions on the horizontal grid of GEOS-Chem (1/2°× 2/3°) to identify correction tendencies relative to the Emission Database for Global Atmospheric Research (EDGAR) v4.2 emission inventory used as a priori. We then cluster these grid cells with a hierarchical algorithm to extract the maximum information from the SCIAMACHY observations. A 1000 cluster ensemble can be adequately constrained, providing~100 km resolution across North America. and Environmental Protection Agency (EPA) inventories, respectively. We find that U.S. livestock emissions are 40% greater than in these two inventories. No such discrepancy is apparent for overall U.S. oil and gas emissions, although this may reflect some compensation between overestimate of emissions from storage/distribution and underestimate from production. We find that U.S. livestock emissions are 70% greater than the oil and gas emissions, in contrast to the EDGAR v4.2 and EPA inventories where these two sources are of comparable magnitude.

Several viable but conflicting explanations have been proposed to explain the recent ~8 p.p.b. per year increase in atmospheric methane after 2006, equivalent to net emissions increase of ~25 Tg CH4 per year. A concurrent increase in atmospheric ethane implicates a fossil source; a concurrent decrease in the heavy isotope content of methane points toward a biogenic source, while other studies propose a decrease in the chemical sink (OH). Here we show that biomass burning emissions of methane decreased by 3.7 (±1.4) Tg CH4 per year from the 2001–2007 to the 2008–2014 time periods using satellite measurements of CO and CH4, nearly twice the decrease expected from prior estimates. After updating both the total and isotopic budgets for atmospheric methane with these revised biomass burning emissions (and assuming no change to the chemical sink), we find that fossil fuels contribute between 12–19 Tg CH4 per year to the recent atmospheric methane increase, thus reconciling the isotopic- and ethane-based results.

SignificanceEmissions of nitrogen oxides (NOx) have a large impact on air quality and climate change as precursors in the formation of ozone and secondary aerosols. We find that NOx emissions have not been decreasing as expected in recent years (2011–2015) when comparing top-down estimates from satellites and surface NO2 measurements to the trends predicted from the US Environmental Protection Agency’s emission inventory data. The discrepancy can be explained by the growing relative contribution of industrial, area, and off-road mobile sources of emissions, decreasing relative contribution of on-road gasoline vehicles, and slower than expected decreases in on-road diesel NOx emissions, with implications for air-quality management.