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Key long-lived greenhouse gases (CO2, CH4, and N2O) are perhaps among the best-studied components of the Earth's atmosphere today; however, attempts to predict or explain trends or even shorter-term variations of these trace gases are not always successful. Infrared spectroscopy is a recognized technique for the ground-based long-term monitoring of the gaseous composition of the atmosphere. The current paper is focused on the analysis of new data on CO2, CH4, and N2O total columns (TCs) retrieved from high resolution IR solar spectra acquired during 2009–2022 at the NDACC atmospheric monitoring station of St. Petersburg State University (STP station, 59.88°N, 29.83°E, 20 m asl.). The paper provides information on the FTIR system (Fourier-transform infrared) installed at the STP station, and an overview of techniques used for the CO2, CH4, and N2O retrievals. Trends of key greenhouse gases and their confidence levels were evaluated using an original approach which combines the Lomb–Scargle method with the cross-validation and bootstrapping techniques. As a result, the following fourteen-year (2009–2022) trends of TCs have been revealed: (0.56 ± 0.01) % yr−1 for CO2; (0.46 ± 0.02) % yr−1 for CH4; (0.28 ± 0.01) % yr−1 for N2O. A comparison with trends based on the EMAC numerical modeling data was carried out. The trends of greenhouse gases observed at the STP site are consistent with the results of the in situ monitoring performed at the same geographical location, and with the independent estimates of the global volume mixing ratio growth rates obtained by the GAW network and the NOAA Global Monitoring Laboratory. There is reasonable agreement between the CH4 and N2O TC trends for 2009–2019, which have been derived from FTIR measurements at three locations: the STP site, Izaña Observatory and the University of Toronto Atmospheric Observatory. [ABSTRACT FROM AUTHOR]

Carbon dioxide (CO2) is a known greenhouse gas and one of the largest contributors to global warming in the Earth's atmosphere. The remote detection and measurement of CO2 from industrial emissions are not routinely carried out and are typically calculated from the fuel combusted or measured directly within ducted vents. However, these methods are not applicable for the quantification of fugitive emissions of CO2. This work presents the results of remote measurement of CO2 emissions using the differential absorption lidar (DIAL) technique at a wavelength of ~2 µm. The results from the DIAL measurements compare well with simultaneous in-stack measurements, these datasets were plotted against each other and can be described by a linear regression of y (t/h) = 1.04 x − 0.02, suggesting any bias in the DIAL data is likely small. Moreover, using the definition outlined in EN 15267-3 a lower detection limit of 0.12 t/h was estimated for the 2 µm wavelength DIAL data, this is three orders of magnitude lower than the corresponding CO2 detection limit measured by NPL in the 1.5 µm wavelength region. Thus, this paper demonstrates the feasibility of high-resolution, ground-based DIAL measurements for quantifying industrial CO2 emissions. [ABSTRACT FROM AUTHOR]

Comparing satellite retrieval with high-precision ground observations is an essential component for the validation of CO2 satellite products. The initial stage of assessing the bias in retrieval products from satellite and ground sources involves establishing a geographical connection between observations that are temporally and spatially proximate. The primary aim of this paper is to evaluate the influence of variations in neighborhood definitions and colocation methods on the assessment of satellite products and provide quantitative references. To achieve this, a series of experiments were conducted involving the Global Total Column Carbon Observation Network (TCCON) and the OCO-2 satellite. Various spatial-temporal neighborhoods and colocation methods were considered in these experiments. The results indicate that spatial neighborhoods exert a more substantial influence on bias compared to temporal neighborhoods. In the mid-latitudes of the Northern Hemisphere, there is an observed linear increase trend between the difference of OCO-2 and TCCON observations and the spatial neighborhood, with an average increase of 0.32 ppm as the neighborhood size changes from 1 ° to 10 ° . Regarding colocation methods, the simple spatiotemporal geographic constraints tend to overlook changes in the atmospheric state to a certain extent. The target geographic constraint method reduces the bias by 2% to 5% by increasing the proportion of OCO-2 observations targeting TCCON while the method of introducing T700 potential temperature reduces by 2% to 13% by screening the gradient of CO2 concentration change. Moreover, an evident correlation exists between the bias and their corresponding latitudes, with a 0.20 ppm increase in bias observed for every 10 ° increment in latitudes in the Northern Hemisphere. The bias of TCCON and OCO-2 shows a pronounced seasonal regularity, with the highest in summer. The study also discusses the selection of spatiotemporal matching with low satellite coverage, the bias distribution, and the attribution of bias to the natural wind field. [ABSTRACT FROM AUTHOR]

Carbon dioxide (CO2) is one of the main greenhouse gases leading to global warming, and the ocean is the largest carbon reservoir on the earth that plays an important role in regulating CO2 concentration on a global scale. The column-averaged dry-air mole fraction of atmospheric CO2 (XCO2) is a key parameter in describing ocean carbon content. In this paper, the Data Interpolation Empirical Orthogonal Function (DINEOF) and the Bayesian Maximum Entropy (BME) methods are combined to interpolate XCO2 data of Orbiting Carbon Observatory 2 (OCO-2) and Orbiting Carbon Observatory 3 (OCO-3) from January to December 2020 occurring within the geographical range of 15–45°N and 120–150°E. At the first stage of our proposed analysis, spatiotemporal information was used by the DINEOF method to perform XCO2 interpolation that improved data coverage; at the second stage, the DINEOF-generated interpolation results were regarded as soft data and were subsequently assimilated using the BME method to obtain improved XCO2 interpolation values. The performance of the synthetic DINEOF–BME interpolation method was evaluated by means of a five-fold cross-validation method. The results showed that the Mean Absolute Error (MAE), the Root Mean Square Error (RMSE), and the Bias of the DINEOF-based OCO-2 and OCO-3 interpolations were 2.106 ppm, 3.046 ppm, and 1.035 ppm, respectively. On the other hand, the MAE, RMSE, and Bias of the cross-validation results obtained by the DINEOF–BME were 1.285 ppm, 2.422 ppm, and −0.085 ppm, respectively, i.e., smaller than the results obtained by DINEOF. In addition, based on the in situ measured XCO2 data provided by the Total Carbon Column Observing Network (TCCON), the original OCO-2 and OCO-3 data were combined and compared with the interpolated products of the synthetic DINEOF–BME framework. The accuracy of the original OCO-2 and OCO-3 products is lower than the DINEOF–BME-generated XCO2 products in terms of MAE (1.751 ppm vs. 2.616 ppm), RMSE (2.877 ppm vs. 3.566 ppm) and Bias (1.379 ppm vs 1.622 ppm), the spatiotemporal coverage of XCO2 product also improved dramatically from 16% to 100%. Lastly, this study demonstrated the feasibility of the synthetic DINEOF–BME approach for XCO2 interpolation purposes and the ability of the BME method to be successfully combined with other techniques. [ABSTRACT FROM AUTHOR]

The traditional field-based measurements of carbon dioxide (pCO2) for inland waters are a snapshot of the conditions on a particular site, which might not adequately represent the pCO2 variation of the entire lake. However, these field measurements can be used in the pCO2 remote sensing modeling and verification. By focusing on inland waters (including lakes, reservoirs, rivers, and streams), this paper reviews the temporal and spatial variability of pCO2 based on published data. The results indicate the significant daily and seasonal variations in pCO2 in lakes. Rivers and streams contain higher pCO2 than lakes and reservoirs in the same climatic zone, and tropical waters typically exhibit higher pCO2 than temperate, boreal, and arctic waters. Due to the temporal and spatial variations of pCO2, it can differ in different inland water types in the same space-time. The estimation of CO2 fluxes in global inland waters showed large uncertainties with a range of 1.40–3.28 Pg C y−1. This paper also reviews existing remote sensing models/algorithms used for estimating pCO2 in sea and coastal waters and presents some perspectives and challenges of pCO2 estimation in inland waters using remote sensing for future studies. To overcome the uncertainties of pCO2 and CO2 emissions from inland waters at the global scale, more reliable and universal pCO2 remote sensing models/algorithms will be needed for mapping the long-term and large-scale pCO2 variations for inland waters. The development of inverse models based on dissolved biogeochemical processes and the machine learning algorithm based on measurement data might be more applicable over longer periods and across larger spatial scales. In addition, it should be noted that the remote sensing-retrieved pCO2/the CO2 concentration values are the instantaneous values at the satellite transit time. A major technical challenge is in the methodology to transform the retrieved pCO2 values on time scales from instant to days/months, which will need further investigations. Understanding the interrelated control and influence processes closely related to pCO2 in the inland waters (including the biological activities, physical mixing, a thermodynamic process, and the air–water gas exchange) is the key to achieving remote sensing models/algorithms of pCO2 in inland waters. This review should be useful for a general understanding of the role of inland waters in the global carbon cycle. [ABSTRACT FROM AUTHOR]

Nighttime light data can characterize urbanization, economic development, population density, energy consumption and other human activities. Additionally, carbon dioxide (CO2) emissions are closely related to the scope and intensity of human activities. In this study, we assess the utility of nighttime light data as a powerful tool to reflect CO2 emissions from energy consumption, analyze the uncertainty associated with different nighttime light data for modeling CO2 emissions, and provide guidance and a reference for modeling CO2 emissions based on nighttime light data. In this paper, Mainland China was taken as a case study, and nighttime light datasets (the Defense Meteorological Satellite Program's Operational Linescan System (DMSP-OLS) nighttime light data and the Suomi National Polar-Orbiting Partnership Visible Infrared Imaging Radiometer Suite (NPP-VIIRS) nighttime light data) as well as a global gridded CO2 emissions dataset (PKU-CO2) were used to perform simple regressions at provincial, prefectural and 0.1° × 0.1° grid levels, respectively. The analyses are aimed at exploring the accuracy and uncertainty of DMSP-OLS and NPP-VIIRS nighttime light data in modeling CO2 emissions at different spatial scales. The improvement of nighttime light index and the potential factors influencing the effects of modeling CO2 emissions based on nighttime light datasets were also explored. The results show that DMSP-OLS is superior to NPP-VIIRS in modeling CO2 emissions at all spatial scales, and the bigger the scale, the more evident the advantages of DMSP-OLS. When modeling CO2 emissions with nighttime light datasets, not only the total amount of lights within a given statistical unit but also the agglomeration degree of lights should be taken into account. Furthermore, the geographical location and socio-economic conditions at the study site, such as gross regional product per capita (GRP per capita), population, and urbanization were shown to have an impact on the regression effect of the nighttime lights-CO2 emissions model. The regression effect was found to be better at higher latitude and longitude areas with higher GRP per capita and higher urbanization, while population showed little effect on the regression effect of the nighttime lights - CO2 emissions model. The limitation of this study is that the thresholds of potential factors are unclear and the quantitative guidance is insufficient. [ABSTRACT FROM AUTHOR]

The Bering Sea, one of the largest and most productive marginal seas, is a crucial carbon sink for the marine carbonate system. However, restricted by the tough observation conditions, few underway datasets of sea surface partial pressure of carbon dioxide (pCO2) have been obtained, with most of them in the eastern areas. Satellite remote sensing data can provide valuable information covered by a large area synchronously with high temporal resolution for assessments of pCO2 that subsequently allow quantification of air-sea carbon dioxide 2 flux. However, pCO2 in the Bering Sea is controlled by multiple factors and thus it is hard to develop a remote sensing algorithm with empirical regression methods. In this paper pCO2 in the Bering Sea from July to September was derived based on a mechanistic semi-analytical algorithm (MeSAA). It was assumed that the observed pCO2 can be analytically expressed as the sum of individual components controlled by major factors. First, a reference water mass that was minimally influenced by biology and mixing was identified in the central basin, and then thermodynamic and biological effects were parameterized for the entire area. Finally, we estimated pCO2 with satellite temperature and chlorophyll data. Satellite results agreed well with the underway observations. Our study suggested that throughout the Bering Sea the biological effect on pCO2 was more than twice as important as temperature, and contributions of other effects were relatively small. Furthermore, satellite observations demonstrate that the spring phytoplankton bloom had a delayed effect on summer pCO2 but that the influence of this biological event varied regionally; it was more significant on the continental slope, with a later bloom, than that on the shelf with an early bloom. Overall, the MeSAA algorithm was not only able to estimate pCO2 in the Bering Sea for the first time, but also provided a quantitative analysis of the contribution of various processes that influence pCO2. [ABSTRACT FROM AUTHOR]

This paper provides an overview of the validation of National Oceanic and Atmospheric Administration (NOAA) operational retrievals of atmospheric carbon trace gas profiles, specifically carbon monoxide (CO), methane (CH4) and carbon dioxide (CO2), from the NOAA-Unique Combined Atmospheric Processing System (NUCAPS), a NOAA enterprise algorithm that retrieves atmospheric profile environmental data records (EDRs) under global non-precipitating (clear to partly cloudy) conditions. Vertical information about atmospheric trace gases is obtained from the Cross-track Infrared Sounder (CrIS), an infrared Fourier transform spectrometer that measures high resolution Earth radiance spectra from NOAA operational low earth orbit (LEO) satellites, including the Suomi National Polar-orbiting Partnership (SNPP) and follow-on Joint Polar Satellite System (JPSS) series beginning with NOAA-20. The NUCAPS CO, CH4, and CO2 profile EDRs are rigorously validated in this paper using well-established independent truth datasets, namely total column data from ground-based Total Carbon Column Observing Network (TCCON) sites, and in situ vertical profile data obtained from aircraft and balloon platforms via the NASA Atmospheric Tomography (ATom) mission and NOAA AirCore sampler, respectively. Statistical analyses using these datasets demonstrate that the NUCAPS carbon gas profile EDRs generally meet JPSS Level 1 global performance requirements, with the absolute accuracy and precision of CO 5% and 15%, respectively, in layers where CrIS has vertical sensitivity; CH4 and CO2 product accuracies are both found to be within ±1%, with precisions of ≈1.5% and ⪅0.5%, respectively, throughout the tropospheric column. [ABSTRACT FROM AUTHOR]

Nitrous oxide (N2O) is a potent and long-lived greenhouse gas that contributes to global warming with a global warming potential (GWP) 298 times that of carbon dioxide (CO2). In this paper, we analyzed the trend of N2O concentration in vertical layers of the stratosphere from 2005 to 2020 using the N2O observed from the Microwave Limb Sounder (MLS) that is on board the Aura satellite. We found that the local N2O concentration showed a downward trend in the lower stratosphere but rose or fluctuated in the upper stratosphere. The reduction reached −5 ppb/yr at pressure levels of 31.62 hPa and 68.13 hPa, with a confidence level of over 90%. The growth was around 1–2 ppb/yr in the upper stratosphere. In addition, a concentration anomaly was observed in the tropical stratosphere in 2013. After the appearance of this anomaly, the N2O concentration in the middle and lower layers of the tropical stratosphere was lower than before 2013. We speculated that the enhancement of the Brewer–Dobson circulation (BDC) upwelling before and after stratospheric sudden warming (SSW) is the main reason for the abnormal concentration distribution in 2013. Stratospheric N2O has changed significantly in the past 16 years with the mutual coupling effect of BDC and SSW and such changes can have further impact on the chemical equilibrium and radiation balance in the stratosphere, as well as on the persistent climate-warming trend. [ABSTRACT FROM AUTHOR]

The Greenhouse Gases Monitoring Instrument (GMI), on board the Chinese Gaofen-5 (GF-5) satellite, provides rich observation data for the global remote sensing of atmospheric CO2. To meet the high-precision satellite retrieval needs of atmospheric CO2, this paper designs a coupled bidirectional reflectance distribution function (BRDF) CO2 retrieval (CBCR) method, which describes the surface reflectance characteristics by the BRDF, corrects for atmospheric scattering based on full physics retrieval theory, and ensures the stable retrieval of multiple parameters and atmospheric CO2 by enriching prior constraints. Theoretical analysis shows that the influence of atmospheric scattering induced by the surface bidirectional reflectance characteristics is significantly related to the aerosol optical depth (AOD), solar zenith angle (SZA), and viewing zenith angle (VZA). The validation of GMI CO2 retrievals shows that the CBCR method significantly reduced the influence of the surface bidirectional reflectance characteristics under high AOD and high SZA conditions, decreased the atmospheric CO2 retrieval error from 0.58 ± 5.64 ppm to −1.33 ± 3.13 ppm, and increased the correlation with the temporal variation of actual atmospheric CO2 from 34.7 to 76.8%. Our CBCR method can correct the influence of atmospheric scattering induced by the surface bidirectional reflectance characteristics on atmospheric CO2 retrieval, and this work demonstrates that describing the surface reflectance characteristics by using BRDF is a promising idea in the field of satellite CO2 retrievals. [ABSTRACT FROM AUTHOR]

This paper presents a comparison of CO2 products derived from Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY), Greenhouse Gases Observing Satellite (GOSAT) and Atmospheric Infrared Sounder (AIRS), with reference to calibration data obtained using the high-resolution ground-based Fourier Transform Spectrometers (g-b FTS) in the Total Carbon Column Observing Network (TCCON). Based on the monthly averages, we calculate the global offsets and regional relative precisions between satellite products and g-b FTS measurements. The results are as follows: the monthly means of SCIAMACHY data are systemically slightly lower than g-b FTS, but limited in coverage; the GOSAT data are superior in stability, but inferior in systematic error; the mean difference between AIRS data and that of g-b FTS is small; and the monthly global coverage is above 95%. Therefore, the AIRS data are better than the other two satellite products in both coverage and accuracy. We also estimate linear trends based on monthly mean data and find that the differences between the satellite products and the g-b FTS data range from 0.25 ppm (SCIAMACHY) to 1.26 ppm (AIRS). The latitudinal distributions of the zonal means of the three satellite products show similar spatial features. The seasonal cycle of satellite products also illustrates the same trend with g-b FTS observations. [ABSTRACT FROM AUTHOR]

Fast radiative transfer models (RTMs) are required to process a great amount of satellite-based atmospheric composition data. Specifically designed acceleration techniques can be incorporated in RTMs to simulate the reflected radiances with a fine spectral resolution, avoiding time-consuming computations on a fine resolution grid. In particular, in the cluster low-streams regression (CLSR) method, the computations on a fine resolution grid are performed by using the fast two-stream RTM, and then the spectra are corrected by using regression models between the two-stream and multi-stream RTMs. The performance enhancement due to such a scheme can be of about two orders of magnitude. In this paper, we consider a modification of the CLSR method (which is referred to as the double CLSR method), in which the single-scattering approximation is used for the computations on a fine resolution grid, while the two-stream spectra are computed by using the regression model between the two-stream RTM and the single-scattering approximation. Once the two-stream spectra are known, the CLSR method is applied the second time to restore the multi-stream spectra. Through a numerical analysis, it is shown that the double CLSR method yields an acceleration factor of about three orders of magnitude as compared to the reference multi-stream fine-resolution computations. The error of such an approach is below 0.05%. In addition, it is analysed how the CLSR method can be adopted for efficient computations for atmospheric scenarios containing aerosols. In particular, it is discussed how the precomputed data for clear sky conditions can be reused for computing the aerosol spectra in the framework of the CLSR method. The simulations are performed for the Hartley–Huggins, O 2 A-, water vapour and CO 2 weak absorption bands and five aerosol models from the optical properties of aerosols and clouds (OPAC) database. [ABSTRACT FROM AUTHOR]

Carbon dioxide (CO2) is a significant atmospheric greenhouse gas and its concentrations can be observed by in situ surface stations, aircraft flights and satellite sensors. This paper investigated the ability of the CO2 satellite observations to monitor, analyze and predict the horizontal and vertical distribution of atmospheric CO2 concentration at global scales. CO2 observations retrieved by an Atmospheric Infrared Sounder (AIRS) were inter-compared with the Global Atmosphere Watch Program (GAW) and HIAPER Pole-to-Pole Observations (HIPPOs), with reference to the measurements obtained using high-resolution ground-based Fourier Transform Spectrometers (FTS) in the Total Carbon Column Observing Network (TCCON) from near-surface level to the mid-to-high troposphere. After vertically integrating the AIRS-retrieved values with the column averaging kernels of TCCON measurements, the AIRS observations are spatio-temporally compared with HIPPO-integrated profiles in the mid-to-high troposphere. Five selected GAW stations are used for comparisons with TCCON sites near the surface of the Earth. The results of AIRS, TCCON (5–6 km), GAW and TCCON (1 km) CO2 measurements from 2007 to 2013 are compared, analyzed and discussed at their respective altitudes. The outcomes indicate that the difference of about 3.0 ppmv between AIRS and GAW or other highly accurate in situ surface measurements is mainly due to the different vertical altitudes, rather than the errors in the AIRS. The study reported here also explores the potential of AIRS satellite observations for analyzing the spatial distribution and seasonal variation of CO2 concentration at global scales. [ABSTRACT FROM AUTHOR]

As one of the most influential greenhouse gases, carbon dioxide (CO2) has a profound impact on the global climate. The spaceborne integrated path differential absorption (IPDA) lidar will be a great sensor to obtain the columnar concentration of CO2 with high precision. This paper analyzes the performance of a spaceborne IPDA lidar, which is part of the Aerosol and Carbon Detection Lidar (ACDL) developed in China. The line-by-bine radiative transfer model was used to calculate the absorption spectra of CO2 and H2O. The laser transmission process was simulated and analyzed. The sources of random and systematic errors of IPDA lidar were quantitatively analyzed. The total systematic errors are 0.589 ppm. Monthly mean global distribution of relative random errors (RREs) was mapped based on the dataset in September 2016. Afterwards, the seasonal variations of the global distribution of RREs were studied. The global distribution of pseudo satellite measurements for a 16-day orbit repeat cycle showed relatively uniform distribution over the land of the northern hemisphere. The results demonstrated that 61.24% of the global RREs were smaller than 0.25%, or about 1 ppm, while 2.76% of the results were larger than 0.75%. The statistics reveal the future performance of the spaceborne IPDA lidar. [ABSTRACT FROM AUTHOR]

Accurate visualization of air temperature distribution can be useful for various thermal analyses in fields such as human health and heat transfer of local area. This paper presents a novel approach to measuring air temperature from midwave hyperspectral Fourier transform infrared (FTIR) imaging in the carbon dioxide absorption band (between 4.25–4.35 μ m). In this study, the proposed visual air temperature (VisualAT) measurement is based on the observation that the carbon dioxide band shows zero transmissivity at short distances. Based on analysis of the radiative transfer equation in this band, only the path radiance by air temperature survives. Brightness temperature of the received radiance can provide the raw air temperature and spectral average, followed by a spatial median-mean filter that can produce final air temperature images. Experiment results tested on a database obtained by a midwave extended FTIR system (Telops, Quebec City, QC, Canada) from February to July 2018 show a mean absolute error of 1.25 ∘ K for temperature range of 2.6−26.4 ∘ C. [ABSTRACT FROM AUTHOR]

NASA's carbon dioxide mission, Orbiting Carbon Observatory-2, began operating in September 2014. In this paper, we analyze four years (2015–2018) of global (60°S–60°N) XCO2 anomalies and their annual variations and seasonal patterns. We show that the anomaly patterns in the column-averaged CO2 dry air mole fraction, XCO2, are robust and consistent from year-to-year. We evaluate the method by comparing the anomalies to fluxes from anthropogenic, biospheric, and biomass burning and to model-simulated local concentration enhancements. We find that, despite the simplicity of the method, the anomalies describe the spatio-temporal variability of XCO2 (including anthropogenic emissions and seasonal variability related to vegetation and biomass burning) consistently with more complex model-based approaches. We see, for example, that positive anomalies correspond to fossil fuel combustion over the major industrial areas (e.g., China, eastern USA, central Europe, India, and the Highveld region in South Africa), shown as large positive XCO2 enhancements in the model simulations. We also find corresponding positive anomalies and fluxes over biomass burning areas during different fire seasons. On the other hand, the largest negative anomalies correspond to the growing season in the northern middle latitudes, characterized by negative XCO2 enhancements from simulations and high solar-induced chlorophyll fluorescence (SIF) values (indicating the occurrence of photosynthesis). The largest discrepancies between the anomaly patterns and the model-based results are observed in the tropical regions, where OCO-2 shows persistent positive anomalies over every season of every year included in this study. Finally, we demonstrate how XCO2 anomalies enable the detection of anthropogenic signatures for several local scale case studies, both in the Northern and Southern Hemisphere. In particular, we analyze the XCO2 anomalies collocated with the recent TROPOspheric Monitoring Instrument NO2 observations (used as indicator of anthropogenic fossil fuel combustion) over the Highveld region in South Africa. The results highlight the capability of satellite-based observations to monitor natural and man-made CO2 signatures on global scale. [ABSTRACT FROM AUTHOR]