Abstract

Abstract. We compare MOPITT Version 7 (V7) Level 2 (L2) and Level 3 (L3) carbon monoxide (CO) products for the 1∘×1∘ L3 grid box containing the coastal city of Halifax, Canada (longitude −63.58∘, latitude 44.65∘), with a focus on the seasons DJF and JJA, and highlight a limitation in the L3 products that has significant consequences for the temporal trends in near-surface CO identified using those data. Because this grid box straddles the coastline, the MOPITT L3 products are created from the finer spatial resolution L2 products that are retrieved over both land and water, with a greater contribution from retrievals over water because more of the grid box lies over water than land. We create alternative L3 products for this grid box by separately averaging the bounded L2 retrievals over land (L3L) and water (L3W) and demonstrate that profile and total column CO (TCO) concentrations, retrieved at the same time, differ depending on whether the retrieval took place over land or water. These differences (ΔRET) are greatest in the lower troposphere (LT), where mean retrieved volume mixing ratios (VMRs) are greater in L3W than L3L, with maximum mean differences of 11.6 % (14.3 ppbv, p=0.001) at the surface level in JJA. Retrieved CO concentrations are more similar, on average, in the middle and upper troposphere (MT and UT), although large differences (in excess of 40 %) do infrequently occur. TCO is also greater in L3W than L3L in both seasons. By analysing L3L and L3W retrieval averaging kernels and simulations of these retrievals, we demonstrate that, in JJA, ΔRET is strongly influenced by differences in retrieval sensitivity over land and water, especially close to the surface where L3L has significantly greater information content than L3W. In DJF, land–water differences in retrieval sensitivity are much less pronounced and appear to have less of an impact on ΔRET, which analysis of wind directions suggests is more likely to reflect differences in true profile concentrations (i.e. real differences). The original L3 time series for the 1∘×1∘ grid box containing Halifax (L3O) corresponds much more closely to L3W than L3L, owing to the greater contribution from L2 retrievals over water than land. Thus, in JJA, variability in retrieved CO concentrations close to the surface in L3O is suppressed compared to L3L, and a declining trend detected using weighted least squares (WLS) regression analysis is significantly slower in L3O (strongest surface level trend identifiable is −1.35 (±0.35) ppbv yr−1) than L3L (−2.85 (±0.60) ppbv yr−1). This is because contributing L2 retrievals over water are closely tied to a priori CO concentrations used in the retrieval, owing to their lack of near-surface sensitivity in JJA, and these are based on monthly climatological CO profiles from a chemical transport model and therefore have no yearly change (surface level trend in L3W is −0.60 (±0.33) ppbv yr−1). Although our analysis focuses on DJF and JJA, we demonstrate that the findings also apply to MAM and SON. The results that we report here suggest that similar analyses be performed for other coastal cities before using MOPITT surface CO.

Highlights

  • The Measurement of Pollution in the Troposphere (MOPITT – Drummond et al, 2010, 2016; abbreviations are defined in Appendix A) instrument is one of a large fleet of satelliteborne instruments capable of observing the composition of the Earth’s atmosphere from space

  • We outline the impact that this has on the statistics of the resulting Level 3 (L3) carbon monoxide (CO) profiles, and we demonstrate the consequences that it has for temporal trend analysis with the L3 dataset, when compared to the results of the same analysis applied to the underlying Level 2 (L2) data that can be filtered by surface type to maximize information content (Sect. 3.2)

  • We restrict our analysis to days when the L3O surface index is mixed and both L3L and L3W retrievals are present, in order to minimize any potential differences in the true profile between land and water

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Summary

Introduction

The Measurement of Pollution in the Troposphere (MOPITT – Drummond et al, 2010, 2016; abbreviations are defined in Appendix A) instrument is one of a large fleet of satelliteborne instruments capable of observing the composition of the Earth’s atmosphere from space. The proportion of information about CO concentrations in each individual retrieval that comes directly from the satellite measurement, as opposed to the a priori, is highly variable It depends on scene-specific factors such as surface temperature, thermal contrast in the lower troposphere, and the actual (true) CO loading itself, as well as on instrumental noise The greatest information content is associated with daytime retrievals over land, during the summer season (MOPITT Algorithm Development Team, 2017; Deeter et al, 2015) This is where and when thermal contrast conditions are typically greatest, maximizing the instrument’s ability to sense CO absorption in the lowermost layers of the troposphere against the hot surface emission background (Deeter et al, 2007; Worden et al, 2010).

Instrument and retrieval overview
Surface type classification
Retrieval simulation
Additional datasets
Results and discussion
Climatology of land–water retrieval and a priori differences
Climatology of land–water retrieval sensitivity differences
Control of RET by land–water sensitivity differences
Regional land–water contrast in L2 data
Consequences for L3O time series
Impact on seasonal data distribution
Consequences for temporal trend analysis
Consideration of MAM and SON
Conclusions
Full Text
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