Abstract

Abstract. The TROPOspheric Monitoring Instrument (TROPOMI) provides a daily, spatially resolved (initially 7×7 km2, upgraded to 7×5.6 km2 in August 2019) global dataset of CO columns; however, due to the relative sparseness of reliable ground-based data sources, it can be challenging to characterize the validity and accuracy of satellite data products in remote regions such as the high Arctic. In these regions, satellite intercomparisons can supplement model- and ground-based validation efforts and serve to verify previously observed differences. In this paper, we compare the CO products from TROPOMI, the Atmospheric Chemistry Experiment (ACE) Fourier transform spectrometer (FTS), and a high-Arctic ground-based FTS located at the Polar Environment Atmospheric Research Laboratory (PEARL) in Eureka, Nunavut (80.05∘ N, 86.42∘ W). A global comparison of TROPOMI reference profiles scaled by the retrieved total column with ACE-FTS CO partial columns for the period from 28 November 2017 to 31 May 2020 displays excellent agreement between the two datasets (R=0.93) and a small relative bias of -0.83±0.26% (bias ± standard error of the mean). Additional comparisons were performed within five latitude bands: the north polar region (60 to 90∘ N), northern mid-latitudes (20 to 60∘ N), the equatorial region (20∘ S to 20∘ N), southern mid-latitudes (60 to 20∘ S), and the south polar region (90 to 60∘ S). Latitudinal comparisons of the TROPOMI and ACE-FTS CO datasets show strong correlations ranging from R=0.93 (southern mid-latitudes) to R=0.86 (equatorial region) between the CO products but display a dependence of the mean differences on latitude. Positive mean biases of 7.93±0.61 % and 7.21±0.52 % were found in the northern and southern polar regions, respectively, while a negative bias of -9.41±0.55% was observed in the equatorial region. To investigate whether these differences are introduced by cloud contamination, which is reflected in the TROPOMI averaging kernel shape, the latitudinal comparisons were repeated for cloud-covered pixels and clear-sky pixels only, as well as for the unsmoothed and smoothed cases. Clear-sky pixels were found to be biased higher with poorer correlations on average than clear+cloudy scenes and cloud-covered scenes only. Furthermore, the latitudinal dependence on the biases was observed in both the smoothed and unsmoothed cases. To provide additional context to the global comparisons of TROPOMI with ACE-FTS in the Arctic, both satellite datasets were compared against measurements from the ground-based PEARL-FTS. Comparisons of TROPOMI with smoothed PEARL-FTS total columns in the period of 3 March 2018 to 27 March 2020 display a strong correlation (R=0.88); however, a positive mean bias of 14.7±0.16 % was also found. A partial column comparison of ACE-FTS with the PEARL-FTS in the period from 25 February 2007 to 18 March 2020 shows good agreement (R=0.79) and a mean positive bias of 7.89±0.21 % in the ACE-FTS product relative to the ground-based FTS. The magnitude and sign of the mean relative differences are consistent across all intercomparisons in this work, as well as with recent ground-based validation efforts, suggesting that the current TROPOMI CO product exhibits a positive bias in the high-Arctic region. However, the observed bias is within the TROPOMI mission accuracy requirement of ±15 %, providing further confirmation that the data quality in these remote high-latitude regions meets this specification.

Highlights

  • Carbon monoxide (CO) is an atmospheric pollutant that is present in relatively low concentrations globally but affects air quality, the climate, and human health

  • We have compared TROPOspheric Monitoring Instrument (TROPOMI), Atmospheric Chemistry Experiment (ACE)-Fourier transform spectrometer (FTS), and a high-Arctic ground-based FTS located in Eureka, Nunavut

  • A global comparison of TROPOMI with Atmospheric Chemistry Experiment Fourier transform spectrometer (ACE-FTS) CO partial columns was performed for the period from 28 November 2017 to 31 May 2020, resulting in excellent agreement, with a Pearson correlation coefficient of R = 0.93 and a mean relative bias of −0.79 ± 0.26 % globally

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Summary

Introduction

Carbon monoxide (CO) is an atmospheric pollutant that is present in relatively low concentrations globally but affects air quality, the climate, and human health. CO has an indirect influence on the global budgets of greenhouse gases such as CH4, CO2, and O3, and it serves as an important sink of the hydroxyl radical (OH), having implications for the chemistry and oxidative power of the atmosphere (Logan et al, 1981; Spivakovsky et al, 2000; Lelieveld et al, 2016). In the remote high-Arctic region, local emissions of CO are negligible, and transported anthropogenic and biomass burning emissions are the primary sources of CO and other reactive species (Yurganov, 1997; Law et al, 2014; Lutsch et al, 2020). Due to its long lifetime in the atmosphere of approximately 2 months, CO serves as an important longrange tracer species for observations of wildfire pollution plumes, in these remote regions (Duflot et al, 2010; Lutsch et al, 2016, 2019). As a result, having accurate and reliable measurements of CO columns over the high Arctic can enable quantification of the role and impacts of biomass burning pollution for the Arctic climate and environment

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