Abstract. The Orbiting Carbon Observatory-2 (OCO-2) carries and points a three-channel imaging grating spectrometer designed to collect high-resolution, co-boresighted spectra of reflected sunlight within the molecular oxygen (O 2 ) Aband at 0.765 microns and the carbon dioxide (CO 2 ) bands at 1.61 and 2.06 microns. These measurements are calibrated and then combined into soundings that are analyzed to retrieve spatially resolved estimates of the column-averaged CO 2 dry-air mole fraction, XCO 2 . Variations of XCO 2 in space and time are then analyzed in the context of the atmospheric transport to quantify surface sources and sinks of CO 2 . This is a particularly challenging remote-sensing observation because all but the largest emission sources and natural absorbers produce only small (< 0.25 %) changes in the background XCO 2 field. High measurement precision is therefore essential to resolve these small variations, and high accuracy is needed because small biases in the retrieved XCO 2 distribution could be misinterpreted as evidence for CO 2 fluxes.To meet its demanding measurement requirements, each OCO-2 spectrometer channel collects 24 spectra s −1 across a narrow (< 10 km) swath as the observatory flies over the sunlit hemisphere, yielding almost 1 million soundings each day. On monthly timescales, between 7 and 12 % of these soundings pass the cloud screens and other data quality filters to yield full-column estimates of XCO 2 . Each of these soundings has an unprecedented combination of spatial resolution (< 3 km 2 /sounding), spectral resolving power (λ/ λ > 17 000), dynamic range (∼ 10 4 ), and sensitivity (continuum signal-to-noise ratio > 400).The OCO-2 instrument performance was extensively characterized and calibrated prior to launch. In general, the instrument has performed as expected during its first 18 months in orbit. However, ongoing calibration and science analysis activities have revealed a number of subtle radiometric and spectroscopic challenges that affect the yield and quality of the OCO-2 data products. These issues include increased numbers of bad pixels, transient artifacts introduced by cosmic rays, radiance discontinuities for spatially non-uniform scenes, a misunderstanding of the instrument polarization orientation, and time-dependent changes in the throughput of the oxygen A-band channel. Here, we describe the OCO-2 instrument, its data products, and its on-orbit performance. We then summarize calibration challenges encountered during its first 18 months in orbit and the methods used to mitigate their impact on the calibrated radiance spectra distributed to the science community.

Abstract. This overview paper highlights the successes of the Ozone Monitoring Instrument (OMI) on board the Aura satellite spanning a period of nearly 14 years. Data from OMI has been used in a wide range of applications and research resulting in many new findings. Due to its unprecedented spatial resolution, in combination with daily global coverage, OMI plays a unique role in measuring trace gases important for the ozone layer, air quality, and climate change. With the operational very fast delivery (VFD; direct readout) and near real-time (NRT) availability of the data, OMI also plays an important role in the development of operational services in the atmospheric chemistry domain.

Abstract. The Orbiting Carbon Observatory-2 (OCO-2) is the first National Aeronautics and Space Administration (NASA) satellite designed to measure atmospheric carbon dioxide (CO 2 ) with the accuracy, resolution, and coverage needed to quantify CO 2 fluxes (sources and sinks) on regional scales. OCO-2 was successfully launched on 2 July 2014 and has gathered more than 2 years of observations. The v7/v7r operational data products from September 2014 to January 2016 are discussed here. On monthly timescales, 7 to 12 % of these measurements are sufficiently cloud and aerosol free to yield estimates of the column-averaged atmospheric CO 2 dry air mole fraction, X CO 2 , that pass all quality tests. During the first year of operations, the observing strategy, instrument calibration, and retrieval algorithm were optimized to improve both the data yield and the accuracy of the products. With these changes, global maps of X CO 2 derived from the OCO-2 data are revealing some of the most robust features of the atmospheric carbon cycle. This includes X CO 2 enhancements co-located with intense fossil fuel emissions in eastern US and eastern China, which are most obvious between October and December, when the north-south X CO 2 gradient is small. Enhanced X CO 2 coincident with biomass burning in the Amazon, central Africa, and Indonesia is also evident in this season. In May and June, when the north-south X CO 2 gradient is largest, these sources are less apparent in global maps. During this part of the year, OCO-2 maps show a more than 10 ppm reduction in X CO 2 across the Northern Hemisphere, as photosynthesis by the land biosphere rapidly absorbs CO 2 . As the carbon cycle science community continues to analyze these OCO-2 data, information on regional-scale sources (emitters) and sinks (absorbers) which impart X CO 2 changes on the order of 1 ppm, as well as far more subtle features, will emerge from this high-resolution global dataset.

Abstract. The Los Angeles megacity, which is home to more than 40 % of the population in California, is the second largest megacity in the United States and an intense source of anthropogenic greenhouse gases (GHGs). Quantifying GHG emissions from the megacity and monitoring their spatiotemporal trends are essential to be able to understand the effectiveness of emission control policies. Here we measure carbon dioxide (CO 2 ) and methane (CH 4 ) across the Los Angeles megacity using a novel approach -ground-based remote sensing from a mountaintop site. A Fourier transform spectrometer (FTS) with agile pointing optics, located on Mount Wilson at 1.67 km above sea level, measures reflected nearinfrared sunlight from 29 different surface targets on Mount Wilson and in the Los Angeles megacity to retrieve the slant column abundances of CO 2 , CH 4 and other trace gases above and below Mount Wilson. This technique provides persistent space-and time-resolved observations of path-averaged dry-air GHG concentrations, XGHG, in the Los Angeles megacity and simulates observations from a geostationary satellite. In this study, we combined high-sensitivity measurements from the FTS and the panorama from Mount Wilson to characterize anthropogenic CH 4 emissions in the megacity using tracer-tracer correlations. During the period between September 2011 and October 2013, the observed XCH 4 : XCO 2 excess ratio, assigned to anthropogenic activities, varied from 5.4 to 7.3 ppb CH 4 (ppm CO 2 ) −1 , with an average of 6.4 ± 0.5 ppb CH 4 (ppm CO 2 ) −1 compared to the value of 4.6 ± 0.9 ppb CH 4 (ppm CO 2 ) −1 expected from the California Air Resources Board (CARB) bottom-up emission inventory. Persistent elevated XCH 4 : XCO 2 excess ratios were observed in Pasadena and in the eastern Los Angeles megacity. Using the FTS observations on Mount Wilson and the bottom-up CO 2 emission inventory, we derived a topdown CH 4 emission of 0.39 ± 0.06 Tg CH 4 year −1 in the Los Angeles megacity. This is 18-61 % larger than the state government's bottom-up CH 4 emission inventory and consistent with previous studies.

We present satellite based ozone profile estimates derived by combining radiances measured at thermal infrared (TIR) wavelengths from the Aura Tropospheric Emission Spectrometer (TES) and ultraviolet (UV) wavelengths measured by the Aura Ozone Monitoring Instrument (OMI). The advantage of using these combined wavelengths and instruments for sounding ozone over either instrument alone is improved sensitivity near the surface as well as the capability to consistently resolve the lower troposphere, upper troposphere, and lower stratosphere for scenes with varying geophysical states. For example, the vertical resolution of ozone estimates from either TES or OMI varies strongly by surface albedo and temperature. Typically, TES provides 1.6 degrees of freedom for signal (DOFS) and OMI provides less than 1 DOFS in the troposphere. The combination provides 2 DOFS in the troposphere with approximately 0.4 DOFS for near surface ozone (surface to 700 hPa). We evaluated these new ozone profile estimates with ozonesonde measurements and found that calculated errors for the joint TES and OMI ozone profile estimates are in reasonable agreement with actual errors as derived by the root-mean-square (RMS) difference between the ozonesondes and the joint TES/OMI ozone estimates. We also used a common a priori profile in the retrievals in order to evaluate the capability of different retrieval approaches on capturing near-surface ozone variability. We found that the vertical resolution of the joint TES/OMI ozone profile estimates shows significant improvements on quantifying variations in near-surface ozone with RMS differences of 49.9% and correlation coefficient of R = 0.58 for the TES/OMI near-surface estimates as compared to 67.2% RMS difference and R = 0.33 for TES and 115.8% RMS difference and R = 0.09 for OMI. This comparison removes the impacts of using the climatological a priori in the retrievals. However, it results in artificially large sonde/retrieval differences. The TES/OMI ozone profiles from the production code of joint retrievals will use climatological a priori and therefore will have more realistic ozone estimates than those from using a common a priori volume mixing ratio profile