scholarly journals Spatio-Temporal Validation of AIRS CO2 Observations Using GAW, HIPPO and TCCON

2020 ◽  
Vol 12 (21) ◽  
pp. 3583
Author(s):  
Hui Yang ◽  
Gefei Feng ◽  
Ru Xiang ◽  
Yunjing Xu ◽  
Yong Qin ◽  
...  

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.

2019 ◽  
Author(s):  
Mai Ouchi ◽  
Yutaka Matsumi ◽  
Tomoki Nakayama ◽  
Kensaku Shimizu ◽  
Takehiko Sawada ◽  
...  

Abstract. A novel, practical observation system for measuring tropospheric carbon dioxide (CO2) concentrations using a non-dispersive infrared analyzer carried by a small helium-filled balloon (CO2 sonde), has been developed for the first time. Onboard calibrations, using CO2 standard gases, is possible to measure the vertical profiles of atmospheric CO2 accurately with a 240–400 m altitude resolution. The standard deviations (1σ) of the measured mixing ratios in the laboratory experiments using a vacuum chamber at a temperature of 298 K were approximately 0.6 ppm at 1010 hPa and 1.2 ppm at 250 hPa. Compared with in situ aircraft data, although the difference up to the altitude of 7 km was 0.6 ± 1.2 ppm, this bias and difference were within the precision of the CO2 sonde. In field experiments, the CO2 sonde detected an increase in CO2 concentration in an urban area and a decrease in a forested area near the surface. The CO2 sonde was shown to be a useful instrument for observing and monitoring the vertical profiles of CO2 concentration in the troposphere.


2021 ◽  
Author(s):  
Rory Scarrott ◽  
Fiona Cawkwell ◽  
Mark Jessopp ◽  
Caroline Cusack

<p>The Ocean-surface Heterogeneity MApping (OHMA) algorithm is an objective, replicable approach to map the spatio-temporal heterogeneity of ocean surface waters. It is used to processes hypertemporal, satellite-derived data and produces a single-image surface heterogeneity (SH) dataset for the selected parameter of interest. The product separates regions of dissimilar temporal characteristics. Data validation is challenging because it requires In-situ observations at spatial and temporal resolutions comparable to the hyper-temporal inputs. Validating this spatio-temporal product highlighted the need to optimise existing vessel-based data collection efforts, to maximise exploitation of the rapidly-growing hyper-temporal data resource.</p><p>For this study, the SH was created using hyper-temporal 1km resolution satellite derived Sea Surface Temperature (SST) data acquired in 2011. Underway ship observations of near surface temperature collected on multiple scientific surveys off the Irish coast in 2011 were used to validate the results. The most suitable underway ship SST data were identified in ocean areas sampled multiple times and with representative measurements across all seasons.</p><p>A 3-stage bias reduction approach was applied to identify suitable ocean areas. The first bias reduction addressed temporal bias, i.e., the temporal spread of available In-situ ship transect data across each satellite image pixel. Only pixels for which In-situ data were obtained at least once in each season were selected; resulting in 14 SH image pixels deemed suitable out of a total of 3,677 SH image pixels with available In-situ data. The second bias reduction addressed spatial bias, to reduce the influence of over-sampled areas in an image pixel with a sub-pixel approach. Statistical dispersion measures and statistical shape measures were calculated for each of the sets of sub-pixel values. This gave heterogeneity estimates for each cruise transit of a pixel area. The third bias reduction addressed bias of temporally oversampled seasons. For each transit-derived heterogeneity measure, the values within each season were averaged, before the annual average value was derived across all four seasons in 2011.</p><p>Significant associations were identified between satellite SST-derived SH values, and In-situ heterogeneity measures related to shape; absolute skewness (Spearman’s Rank, n=14, ρ[12]= +0.5755, P<0.05), and kurtosis (Spearman’s Rank, n=14, ρ[12] = 0.5446, P < 0.05). These are a consequence of (i) locally-extreme measurements, and/or (ii) increased presence of sharp transitions detected spatially by In-situ data. However, the number and location of suitable In-situ validation sites precluded a robust validation of the SH dataset (14 pixels located in Irish waters, for a dataset spanning the North Atlantic). This requires more targeted data. The approach would have benefited from more samples over the winter season, which would have enabled more offshore validation sites to be incorporated into the analysis. This is a challenge that faces satellite product developers, who want to deliver spatio-temporal information to new markets. There is a significant opportunity for dedicated, transit-measured (e.g. Ferry box data), validation sites to be established. These could potentially synergise with key nodes in global shipping routes to maximise data collected by vessels of opportunity, and ensure consistent data are collected over the same area at regular intervals.</p>


2021 ◽  
Author(s):  
Enrico Dammers ◽  
Mark Shephard ◽  
Evan White ◽  
Debora Griffin ◽  
Evan Chow ◽  
...  

<p>While ammonia (NH3) at its current levels is known to be a hazard to environmental and human health, the atmospheric budget is still quite uncertain. This can largely be attributed to the short lifetime of ammonia in combination with an overall lack of (dense) in-situ measurement networks. The capability to observe ammonia distributions with satellites has opened new ways to study the atmospheric ammonia budget. Previous studies have demonstrated the capability of current ammonia satellite sensors to resolve emissions from point like sources, biomass burning, and constraining emission sources at a regional level with methods involving the use of air quality models.</p><p>In this study, we present the first spatially resolved ammonia emission estimates across the globe using a consistent methodology based solely on ammonia satellite observations from the Cross-track Infrared Sounder (CrIS) instrument and ECMWF ERA5 wind fields. The concept was evaluated for North Western Europe and demonstrated the ability to constrain annual emissions at county- to provincial-levels with most deviations within the bounds found in the error analysis. Furthermore, we show that for some regions the spatial patterns found in the satellite observations are consistent while others do not match the current inventories. Finally, the results indicate that the absolute emission levels tend to be underestimated for parts of the globe.</p>


2020 ◽  
Vol 12 (3) ◽  
pp. 576 ◽  
Author(s):  
Zhonghua He ◽  
Liping Lei ◽  
Yuhui Zhang ◽  
Mengya Sheng ◽  
Changjiang Wu ◽  
...  

Column-averaged dry air mole fraction of atmospheric CO2 (XCO2), obtained by multiple satellite observations since 2003 such as ENVISAT/SCIAMACHY, GOSAT, and OCO-2 satellite, is valuable for understanding the spatio-temporal variations of atmospheric CO2 concentrations which are related to carbon uptake and emissions. In order to construct long-term spatio-temporal continuous XCO2 from multiple satellites with different temporal and spatial periods of observations, we developed a precision-weighted spatio-temporal kriging method for integrating and mapping multi-satellite observed XCO2. The approach integrated XCO2 from different sensors considering differences in vertical sensitivity, overpass time, the field of view, repeat cycle and measurement precision. We produced globally mapped XCO2 (GM-XCO2) with spatial/temporal resolution of 1 × 1 degree every eight days from 2003 to 2016 with corresponding data precision and interpolation uncertainty in each grid. The predicted GM-XCO2 precision improved in most grids compared with conventional spatio-temporal kriging results, especially during the satellites overlapping period (0.3–0.5 ppm). The method showed good reliability with R2 of 0.97 from cross-validation. GM-XCO2 showed good accuracy with a standard deviation of bias from total carbon column observing network (TCCON) measurements of 1.05 ppm. This method has potential applications for integrating and mapping XCO2 or other similar datasets observed from multiple satellite sensors. The resulting GM-XCO2 product may be also used in different carbon cycle research applications with different precision requirements.


Processes ◽  
2020 ◽  
Vol 8 (11) ◽  
pp. 1373
Author(s):  
Amir Izzuddin Adnan ◽  
Mei Yin Ong ◽  
Saifuddin Nomanbhay ◽  
Pau Loke Show

Carbon dioxide is the most influential gas in greenhouse gasses and its amount in the atmosphere reached 412 µmol/mol in August 2020, which increased rapidly, by 48%, from preindustrial levels. A brand-new chemical industry, namely organic chemistry and catalysis science, must be developed with carbon dioxide (CO2) as the source of carbon. Nowadays, many techniques are available for controlling and removing carbon dioxide in different chemical processes. Since the utilization of CO2 as feedstock for a chemical commodity is of relevance today, this study will focus on how to increase CO2 solubility in culture media used for growing microbes. In this work, the CO2 solubility in a different medium was investigated. Sodium hydroxide (NaOH) and monoethanolamine (MEA) were added to the culture media (3.0 g/L dipotassium phosphate (K2HPO4), 0.2 g/L magnesium chloride (MgCl2), 0.2 g/L calcium chloride (CaCl2), and 1.0 g/L sodium chloride (NaCl)) for growing microbes in order to observe the difference in CO2 solubility. Factors of temperature and pressure were also studied. The determination of CO2 concentration in the solution was measured by gas analyzer. The result obtained from optimization revealed a maximum CO2 concentration of 19.029 mol/L in the culture media with MEA, at a pressure of 136.728 kPa, operating at 20.483 °C.


2019 ◽  
Vol 19 (15) ◽  
pp. 9797-9831 ◽  
Author(s):  
Sean Crowell ◽  
David Baker ◽  
Andrew Schuh ◽  
Sourish Basu ◽  
Andrew R. Jacobson ◽  
...  

Abstract. The Orbiting Carbon Observatory-2 has been on orbit since 2014, and its global coverage holds the potential to reveal new information about the carbon cycle through the use of top-down atmospheric inversion methods combined with column average CO2 retrievals. We employ a large ensemble of atmospheric inversions utilizing different transport models, data assimilation techniques, and prior flux distributions in order to quantify the satellite-informed fluxes from OCO-2 Version 7r land observations and their uncertainties at continental scales. Additionally, we use in situ measurements to provide a baseline against which to compare the satellite-constrained results. We find that within the ensemble spread, in situ observations, and satellite retrievals constrain a similar global total carbon sink of 3.7±0.5 PgC yr−1, and 1.5±0.6 PgC yr−1 for global land, for the 2015–2016 annual mean. This agreement breaks down in smaller regions, and we discuss the differences between the experiments. Of particular interest is the difference between the different assimilation constraints in the tropics, with the largest differences occurring in tropical Africa, which could be an indication of the global perturbation from the 2015–2016 El Niño. Evaluation of posterior concentrations using TCCON and aircraft observations gives some limited insight into the quality of the different assimilation constraints, but the lack of such data in the tropics inhibits our ability to make strong conclusions there.


2014 ◽  
Vol 14 (5) ◽  
pp. 2541-2554 ◽  
Author(s):  
S. X. Fang ◽  
L. X. Zhou ◽  
P. P. Tans ◽  
P. Ciais ◽  
M. Steinbacher ◽  
...  

Abstract. Atmospheric carbon dioxide (CO2) mole fractions were continuously measured from January 2009 to December 2011 at four atmospheric observatories in China using cavity ring-down spectroscopy instruments. The stations are Lin'an (LAN), Longfengshan (LFS), Shangdianzi (SDZ), and Waliguan (WLG), which are regional (LAN, LFS, SDZ) or global (WLG) measurement stations of the World Meteorological Organization's Global Atmosphere Watch program (WMO/GAW). LAN is located near the megacity of Shanghai, in China's economically most developed region. LFS is in a forest and rice production area, close to the city of Harbin in northeastern China. SDZ is located 150 km northeast of Beijing. WLG, hosting the longest record of measured CO2 mole fractions in China, is a high-altitude site in northwestern China recording background CO2 concentration. The CO2 growth rates are 3.7 ± 1.2 ppm yr−1 for LAN, 2.7 ± 0.8 ppm yr−1 for LFS, 3.5 ± 1.6 ppm yr−1 for SDZ, and 2.2 ± 0.8 ppm yr−1 (1σ) for WLG during the period of 2009 to 2011. The highest annual mean CO2 mole fraction of 404.2 ± 3.9 ppm was observed at LAN in 2011. A comprehensive analysis of CO2 variations, their diurnal and seasonal cycles as well as the analysis of the influence of local sources on the CO2 mole fractions allows a characterization of the sampling sites and of the key processes driving the CO2 mole fractions. These data form a basis to improve our understanding of atmospheric CO2 variations in China and the underlying fluxes using atmospheric inversion models.


Sensors ◽  
2021 ◽  
Vol 21 (19) ◽  
pp. 6436
Author(s):  
Mai Hu ◽  
Bing Chen ◽  
Lu Yao ◽  
Chenguang Yang ◽  
Xiang Chen ◽  
...  

Research on carbon dioxide (CO2) geological and biogeochemical cycles in the ocean is important to support the geoscience study. Continuous in-situ measurement of dissolved CO2 is critically needed. However, the time and spatial resolution are being restricted due to the challenges of very high submarine pressure and quite low efficiency in water-gas separation, which, therefore, are emerging the main barriers to deep sea investigation. We develop a fiber-integrated sensor based on cavity ring-down spectroscopy for in-situ CO2 measurement. Furthermore, a fast concentration retrieval model using exponential fit is proposed at non-equilibrium condition. The in-situ dissolved CO2 measurement achieves 10 times faster than conventional methods, where an equilibrium condition is needed. As a proof of principle, near-coast in-situ CO2 measurement was implemented in Sanya City, Haina, China, obtaining an effective dissolved CO2 concentration of ~950 ppm. The experimental results prove the feasibly for fast dissolved gas measurement, which would benefit the ocean investigation with more detailed scientific data.


2019 ◽  
Author(s):  
Minqiang Zhou ◽  
Bavo Langerock ◽  
Mahesh Kumar Sha ◽  
Nicolas Kumps ◽  
Christian Hermans ◽  
...  

Abstract. TCCON (Total Carbon Column Observing Network) column-averaged dry air mole fraction of CH4 (XCH4) measurements have been widely used to validate satellite observations and to estimate model simulations. The GGG2014 code is the standard TCCON retrieval software performing a profile scaling retrieval. In order to obtain several vertical information in addition to total column, in this study, the SFIT4 retrieval code is applied to retrieve CH4 mole fraction vertical profile using TCCON spectra (SFIT4TCCON) at six sites (Ny-Ålesund, Sodankylä, Bialystok, Bremen, Orléans and St Denis) during the time period of 2016−2017. The retrieval strategy of SFIT4TCCON is investigated. The degree of freedom for signal of the SFIT4TCCON retrieval is about 2.4, with two distinct species of information in the troposphere and in the stratosphere. The averaging kernel and error budget of the SFIT4TCCON retrieval are presented. The data accuracy and precision of the SFIT4TCCON retrievals, including the total column and two partial columns (in the troposphere and stratosphere), are estimated by TCCON standard retrievals, ground-based in situ measurements, ACE-FTS satellite observations, TCCON proxy data and AirCore measurements. By comparison against TCCON standard retrievals, it is found that the retrieval uncertainty of SFIT4TCCON XCH4 is similar to that of TCCON standard retrievals with the systematic uncertainty within 0.35 % and the random uncertainty about 0.5 %. The tropospheric and stratospheric XCH4 from SFIT4TCCON retrievals are assessed by comparing with AirCore measurements at Sodankylä, and there is a 1.2 % overestimation in the SFIT4TCCON tropospheric XCH4 and a 4.0 % underestimation in the SFIT4TCCON stratospheric XCH4, which are within the systematic uncertainties of SFIT4TCCON retrieved partial columns in the troposphere and stratosphere, respectively.


2021 ◽  
Author(s):  
Juan Cuesta ◽  
Lorenzo Costantino ◽  
Matthias Beekmann ◽  
Guillaume Siour ◽  
Laurent Menut ◽  
...  

Abstract. We present a comprehensive study integrating satellite observations of ozone pollution, in situ measurements and chemistry transport model simulations for quantifying the role of anthropogenic emission reductions during the COVID-19 lockdown in spring 2020 over Europe. Satellite observations are derived from the IASI+GOME2 multispectral synergism, which provides particularly enhanced sensitivity to near-surface ozone pollution. These observations are first analysed in terms of differences between the average on 1–15 April 2020, when the strictest lockdown restrictions took place, and the same period in 2019. They show clear enhancements of near-surface ozone in Central Europe and Northern Italy, and some other hotspots, which are typically characterized by VOC-limited chemical regimes. An overall reduction of ozone is observed elsewhere, where ozone chemistry is limited by the abundance of NOx. The spatial distribution of positive and negative ozone concentration anomalies observed from space is in relatively good quantitative agreement with surface in situ measurements over the continent (a correlation coefficient of 0.55, a root-mean-squared difference of 11 ppb and the same standard deviation and range of variability). An average bias of ∼8 ppb between the two observational datasets is remarked, which can partly be explained by the fact the satellite approach retrieves partial columns of ozone with a peak sensitivity above the surface (near 2 km of altitude). For assessing the impact of the reduction of anthropogenic emissions during the lockdown, we adjust the satellite and in situ surface observations for withdrawing the influence of meteorological conditions in 2020 and 2019. This adjustment is derived from the chemistry transport model simulations using the meteorological fields of each year and identical emission inventories. This observational estimate of the influence of lockdown emission reduction is consistent for both datasets. They both show lockdown-associated ozone enhancements in hotspots over Central Europe and Northern Italy, with a reduced amplitude with respect to the total changes observed between the two years, and an overall reduction elsewhere over Europe and the ocean. Satellite observations additionally highlight the ozone anomalies in the regions remote from in situ sensors, an enhancement over the Mediterranean likely associated with maritime traffic emissions and a marked large-scale reduction of ozone elsewhere over ocean (particularly over the North Sea), in consistency with previous assessments done with ozonesondes measurements in the free troposphere. These observational assessments are compared with model-only estimations, using the CHIMERE chemistry transport model. For analysing the uncertainty of the model estimates, we perform two sets of simulations with different setups, differing in the emission inventories, their modifications to account for changes in anthropogenic activities during the lockdown and the meteorological fields. Whereas a general qualitative consistency of positive and negative ozone anomalies is remarked between all model and observational estimates, significant changes are seen in their amplitudes. Models underestimate the range of variability of the ozone changes by at least a factor 2 with respect to the two observational data sets, both for enhancements and decreases of ozone, while the large-scale ozone decrease is not simulated. With one of the setups, the model simulates ozone enhancements a factor 3 to 6 smaller than with the other configuration. This is partly linked to the emission inventories of ozone precursors (at least a 30 % difference), but mainly to differences in vertical mixing of atmospheric constituents depending on the choice of the meteorological model.


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