Abstract. Global observations of column-averaged dry air mole fractions of carbon dioxide (CO2), denoted by XCO2 , retrieved from SCIAMACHY on-board ENVISAT can provide important and missing global information on the distribution and magnitude of regional CO2 surface fluxes. This application has challenging precision and accuracy requirements. In a previous publication (Heymann et al., 2012), it has been shown by analysing seven years of SCIAMACHY WFM-DOAS XCO2 (WFMDv2.1) that unaccounted thin cirrus clouds can result in significant errors. In order to enhance the quality of the SCIAMACHY XCO2 data product, we have developed a new version of the retrieval algorithm (WFMDv2.2), which is described in this manuscript. It is based on an improved cloud filtering and correction method using the 1.4 μm strong water vapour absorption and 0.76 μm O2-A bands. The new algorithm has been used to generate a SCIAMACHY XCO2 data set covering the years 2003–2009. The new XCO2 data set has been validated using ground-based observations from the Total Carbon Column Observing Network (TCCON). The validation shows a significant improvement of the new product (v2.2) in comparison to the previous product (v2.1). For example, the standard deviation of the difference to TCCON at Darwin, Australia, has been reduced from 4 ppm to 2 ppm. The monthly regional-scale scatter of the data (defined as the mean intra-monthly standard deviation of all quality filtered XCO2 retrievals within a radius of 350 km around various locations) has also been reduced, typically by a factor of about 1.5. Overall, the validation of the new WFMDv2.2 XCO2 data product can be summarised by a single measurement precision of 3.8 ppm, an estimated regional-scale (radius of 500 km) precision of monthly averages of 1.6 ppm and an estimated regional-scale relative accuracy of 0.8 ppm. In addition to the comparison with the limited number of TCCON sites, we also present a comparison with NOAA's global CO2 modelling and assimilation system CarbonTracker. This comparison also shows significant improvements especially over the Southern Hemisphere.
Abstract. Methane is an important atmospheric greenhouse gas and an adequate understanding of its emission sources is needed for climate change assessments, predictions, and the development and verification of emission mitigation strategies. Satellite retrievals of near-surface-sensitive column-averaged dry-air mole fractions of atmospheric methane, i.e. XCH4, can be used to quantify methane emissions. Maps of time-averaged satellite-derived XCH4 show regionally elevated methane over several methane source regions. In order to obtain methane emissions of these source regions we use a simple and fast data-driven method to estimate annual methane emissions and corresponding 1σ uncertainties directly from maps of annually averaged satellite XCH4. From theoretical considerations we expect that our method tends to underestimate emissions. When applying our method to high-resolution atmospheric methane simulations, we typically find agreement within the uncertainty range of our method (often 100 %) but also find that our method tends to underestimate emissions by typically about 40 %. To what extent these findings are model dependent needs to be assessed. We apply our method to an ensemble of satellite XCH4 data products consisting of two products from SCIAMACHY/ENVISAT and two products from TANSO-FTS/GOSAT covering the time period 2003–2014. We obtain annual emissions of four source areas: Four Corners in the south-western USA, the southern part of Central Valley, California, Azerbaijan, and Turkmenistan. We find that our estimated emissions are in good agreement with independently derived estimates for Four Corners and Azerbaijan. For the Central Valley and Turkmenistan our estimated annual emissions are higher compared to the EDGAR v4.2 anthropogenic emission inventory. For Turkmenistan we find on average about 50 % higher emissions with our annual emission uncertainty estimates overlapping with the EDGAR emissions. For the region around Bakersfield in the Central Valley we find a factor of 5–8 higher emissions compared to EDGAR, albeit with large uncertainty. Major methane emission sources in this region are oil/gas and livestock. Our findings corroborate recently published studies based on aircraft and satellite measurements and new bottom-up estimates reporting significantly underestimated methane emissions of oil/gas and/or livestock in this area in EDGAR.
Abstract. Urban areas, which are home to the majority of today's world population, are responsible for more than two-thirds of the global energy-related carbon dioxide emissions. Given the ongoing demographic growth and rising energy consumption in metropolitan regions particularly in the developing world, urban-based emissions are expected to further increase in the future. As a consequence, monitoring and independent verification of reported anthropogenic emissions is becoming more and more important. It is demonstrated using SCIAMACHY nadir measurements that anthropogenic CO2 emissions can be detected from space and that emission trends might be tracked using satellite observations. This is promising with regard to future satellite missions with high spatial resolution and wide swath imaging capability aiming at constraining anthropogenic emissions down to the point-source scale. By subtracting retrieved background values from those retrieved over urban areas we find significant CO2 enhancements for several anthropogenic source regions, namely 1.3 ± 0.7 ppm for the Rhine-Ruhr metropolitan region and the Benelux, 1.1 ± 0.5 ppm for the East Coast of the United States, and 2.4 ± 0.9 ppm for the Yangtze River Delta. The order of magnitude of the enhancements is in agreement with what is expected for anthropogenic CO2 signals. The larger standard deviation of the retrieved Yangtze River Delta enhancement is due to a distinct positive trend of 0.3 ± 0.2 ppm yr−1, which is quantitatively consistent with anthropogenic emissions from the Emission Database for Global Atmospheric Research (EDGAR) in terms of percentual increase per year. Potential contributions to the retrieved CO2 enhancement by several error sources, e.g. aerosols, albedo, and residual biospheric signals due to heterogeneous seasonal sampling, are discussed and can be ruled out to a large extent.
Abstract. Carbon dioxide (CO2) is the most important greenhouse gas whose atmospheric loading has been significantly increased by anthropogenic activity leading to global warming. Accurate measurements and models are needed in order to reliably predict our future climate. This, however, has challenging requirements. Errors in measurements and models need to be identified and minimised. In this context, we present a comparison between satellite-derived column-averaged dry air mole fractions of CO2, denoted XCO2, retrieved from SCIAMACHY/ENVISAT using the WFM-DOAS (weighting function modified differential optical absorption spectroscopy) algorithm, and output from NOAA's global CO2 modelling and assimilation system CarbonTracker. We investigate to what extent differences between these two data sets are influenced by systematic retrieval errors due to aerosols and unaccounted clouds. We analyse seven years of SCIAMACHY WFM-DOAS version 2.1 retrievals (WFMDv2.1) using CarbonTracker version 2010. We investigate to what extent the difference between SCIAMACHY and CarbonTracker XCO2 are temporally and spatially correlated with global aerosol and cloud data sets. For this purpose, we use a global aerosol data set generated within the European GEMS project, which is based on assimilated MODIS satellite data. For clouds, we use a data set derived from CALIOP/CALIPSO. We find significant correlations of the SCIAMACHY minus CarbonTracker XCO2 difference with thin clouds over the Southern Hemisphere. The maximum temporal correlation we find for Darwin, Australia (r2 = 54%). Large temporal correlations with thin clouds are also observed over other regions of the Southern Hemisphere (e.g. 43% for South America and 31% for South Africa). Over the Northern Hemisphere the temporal correlations are typically much lower. An exception is India, where large temporal correlations with clouds and aerosols have also been found. For all other regions the temporal correlations with aerosol are typically low. For the spatial correlations the picture is less clear. They are typically low for both aerosols and clouds, but depending on region and season, they may exceed 30% (the maximum value of 46% has been found for Darwin during September to November). Overall we find that the presence of thin clouds can potentially explain a significant fraction of the difference between SCIAMACHY WFMDv2.1 XCO2 and CarbonTracker over the Southern Hemisphere. Aerosols appear to be less of a problem. Our study indicates that the quality of the satellite derived XCO2 will significantly benefit from a reduction of scattering related retrieval errors at least for the Southern Hemisphere.
Abstract Indonesia experienced an exceptional number of fires in 2015 as a result of droughts related to the recent El Niño event and human activities. These fires released large amounts of carbon dioxide (CO 2 ) into the atmosphere. Emission databases such as the Global Fire Assimilation System version 1.2 and the Global Fire Emission Database version 4s estimated the CO 2 emission to be approximately 1100 MtCO 2 in the time period from July to November 2015. This emission was indirectly estimated by using parameters like burned area, fire radiative power, and emission factors. In the study presented in this paper, we estimate the Indonesian fire CO 2 emission by using the column‐averaged dry air mole fraction of CO 2 , X CO 2 , derived from measurements of the Orbiting Carbon Observatory‐2 satellite mission. The estimated CO 2 emission is 748 ± 209 MtCO 2 , which is about 30% lower than provided by the emission databases.
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