1. Introduction
Forests cover over a third of the total land area of Europe [
1]. Climate change is drastically intensifying the threats to the forests, which are more pronounced in the Mediterranean climate-intense rain in winter and drier summers [
2]. Such factors foster higher levels of vegetation growth and the accumulation of fuel, which both contribute to extreme wildfires. The environmental impact of events between 2000 and 2017 in Europe resulted in losses of 8.5 million burned ha, approximately 480,000 ha/year [
3]. In Portugal’s mainland territory, the burned area in 2018 and 2019 amounted to 44,578 ha and 42,084 ha, respectively, according to the Forest Fires in Europe, Middle East and North Africa report for 2018 and 2019 [
4,
5]. In terms of economic fire impact on the most affected countries, Portugal, for example, may see an increase in losses of over EUR 5 billion/year by 2070–2100 (2.4% of Portugal GDP in 2019, Instituto Nacional de Estatística, INE data).
According to the European Commissioner for Research, Science and Innovation in 2018 [
3], “Making the wealth of knowledge and the implications of such knowledge available to develop forest fires risk mitigation strategies is a pre-requisite to implementing adequate policies and to better protecting European citizens, the economy and the environment against megafires.” Environmental changes, in particular, drainage and forest clearing, threaten the stability of forests [
6], making them susceptible to wildfire events. Wildfires are one of the most significant disturbances to land ecosystems on a regional and global scale, and generate large quantities of critical greenhouse gases [
7]. Extreme wildfires are a major hazard throughout Europe; however, these events are not fully understood. The current models of wildfire spread are still not sufficiently robust to effectively explain the fire’s behavior. Therefore, increasing the resilience and knowledge of society as far as these extreme events are concerned by taking advantage of new technologies such as satellites to gather new and critical data is pivotal to building science-based forest fire management strategies and for risk-informed decision-making.
Wildland fires emit large amounts of trace gases and particles [
8,
9,
10,
11] and these emissions are believed to significantly influence the chemical composition of the atmosphere [
12,
13] and the earth’s climate system. Combustion is a chemical process that results in the oxidation and breakdown of organic matter from living and dead vegetation. The wide variety of pollutants released by wildfires, due to complete or incomplete combustion, include greenhouse gases, carbon dioxide (CO
2) [
14], methane (CH
4), and photochemically reactive compounds such as carbon monoxide (CO) [
15]. In particular, the lifespan of CH
4 in the atmosphere is much shorter than that of CO
2; however, CH
4 is more efficient at trapping radiation than CO
2. The comparative impact of CH
4 is 25 times greater than CO
2 over a 100-year period [
16]. On the other hand, CO is a trace gas in the atmosphere that does not have a direct effect on the global temperature, as does methane; nonetheless, CO plays a major role in atmospheric chemistry, and it affects the ability of the atmosphere to cleanse itself of many other polluting gases and combined with other pollutants and solar radiation, it also takes part in the formation of lower-atmospheric ozone and urban smog. Thus, to enable the development of a mechanistic understanding of the changing role of these drivers (extreme wildfires and their by-product gases) and their impact on atmospheric composition, long-term wildfire records are needed. Satellites are important in improving the knowledge regarding fire events. They are commonly used after the fire to measure the burned area and fire severity, but are also useful to record smoke and gas emissions during the fire, to provide information on firefighting hazards [
17], to predict fire danger, to map fuels, to monitor fire dynamics [
18], and to assess air quality. Many of these objectives are better achieved by merging satellite information and in situ data [
19].
Global Monitoring for Environment and Security (GMES) is a joint initiative of the European Community (EC) and the European Space Agency (ESA). The overall objective of the GMES initiative is to support Europe’s goals regarding sustainable development and the global governance of the environment by providing timely and high-quality data, information, services, and knowledge. The Sentinel-5 Precursor (S5-P) mission is applicable for further integration of the air quality and climate issues at policy level [
20]. The S5-P mission is a single-payload satellite in a low Earth orbit that provides daily global information on concentrations of trace gases and aerosols that are important for air quality [
10]. The payload of the mission is the TROPOspheric Monitoring Instrument (TROPOMI). TROPOMI is a spectrometer with spectral bands in ultraviolet, visible, near-infrared, and shortwave infrared (SWIR). The selected wavelength range for TROPOMI allows for observation of key atmospheric constituents, including ozone, nitrogen dioxide (NO
2), carbon monoxide (CO), sulfur dioxide, methane (CH
4), formaldehyde, aerosols, and clouds [
21]. In addition to other objectives, the S5-P TROPOMI holds the understanding of the atmospheric chemistry related to climate and the chemistry–long-term observational records that are essential to validating the new generation of climate and Earth system models [
20]. Recent studies have shown the potential of TROPOMI for various pollutant emissions. Lama et al. [
22] investigated the use of co-located NO
2 and CO retrievals from the TROPOMI satellite to improve the quantification of burning efficiency and emission factors over different megacities. Additionally, Rooney et al. [
23] conducted a comprehensive investigation of air quality impacts, regarding PM
2.5 emissions on the Camp Fire using a combined analysis of ground-based and space-borne observations and WRF-Chem simulations. A year after, Van der Velde et al. [
24] examined different fire-prone regions around the world by means of an analysis of the biomass burning pollutants through the column measurements of nitrogen dioxide and carbon monoxide provided by TROPOMI, by using space-borne data to investigate the spatiotemporal efficiency of fire combustion.
On this basis, it is key to understand that the increase in CH
4 concentrations, which may be attributed to the increased tropospheric ozone observed in the 20th century [
25], and the transformation of gaseous precursors (e.g., CO) into radiative active constituents, are still poorly quantified. Further insights into these transformation processes are needed to link the climate impact of the primary forcing agents to mitigation options that are related to the gaseous precursor emissions [
20]. Hence, to tackle such challenges, the aim of this study is to ascertain the potential of the S5-P TROPOMI satellite for the monitoring and supervision of CO and CH
4 during wildfire events toward the analysis of (i) Level-2 data products and (ii) their connection with in situ data. Its potentiality is discussed for two particular Portuguese extreme wildfires: Monchique in 2018 and Vila de Rei/Mação in 2019.
3. Results and Discussion
The influence of weather conditions on the spread of any wildfire is fundamental. In the initial attack phase and the first hours of the extended attack, there is a very sharp increase in the energy of the fire, corresponding to a rapid progression with a combined effect of the different factors: fuel, temperature, and wind [
26,
27]. The fuel consists of the vegetation in the area covered by the fire and influences the type of combustion during the wildfire event and, consequently, the CO and CH
4 emissions [
26]. The relative humidity of the air and, in turn, the humidity of the dead fine fuels, typically varies, unlike the temperature of the air. Finally, the wind, the most difficult feature to predict, varies temporally and spatially in its speed and direction, which normally determines the direction of the fire. However, in order to build a solid understanding of wildfire incidents not only requires consideration of these factors but also a body of knowledge correlating in situ and remote sensing data. In Zheng et al. [
34], over the period of one year, the NO
2 column concentration based on remote sensing was found to be strongly correlated (R
2 = 0.72) with ground-based data provided by surface monitoring stations [
35,
36]. Accordingly,
Figure 2 illustrates the CO pattern for S5-P TROPOMI and the measurements made by the surface monitoring station. The David Neto station, located in Portimão, Portugal (lat. 37°8′17.988″ N, long. 8°32′31.992″ W), is included in the matrix area (77 × 77 km
2), and was therefore selected to validate the data provided by the satellite. It should be noted that as the results correspond to a short period (from 27 July to 19 August 2018), the coherence analysis of the Sentinel-5P TROPOMI CO data and the surface monitoring data is ancillary.
It is critical to emphasize that S5-P TROPOMI monitors the geolocated points of interest between 12:00 a.m. and 1:30 p.m. and the surface monitoring data is recorded hourly. Nonetheless, when the data was linked for the timeframe where the measurement corresponded to the overpassing time of the satellite, it was possible to observe a similar pattern in both surface and S5-P TROPOMI data, with a correlation of 50% (multiple R). This correlation shows that the accuracy of the S5-P TROPOMI CO measurements, even with fewer points (when compared to the surface data), was not compromised [
37]. In
Figure 2, a sharp increase for both datasets may be observed on the days of the fire, in particular between 6 and 7 August, the most intense days of fire.
Based on these observations (correlation coefficient and comparable CO emission trend), SP5-P TROPOMI appears to present possible potential to monitor and follow CO fluctuations in each of the fires under study. To evaluate this hypothesis, in the following sections, the Monchique and Vila de Rei/Mação wildfires were explored in consideration of the CO and CH4 spatial distribution, trends, and spatio-temporal analysis provided by S5-P TROPOMI.
Through these analyses, the retrieval uncertainty of CO column and XCH
4 mean average were 0.0011 mol/m
2 and 1.4697 ppb, respectively (the total CO column precision and XCH
4 mixing ratio precision are in
Table S1). It may be noted that for XCH
4 the measurements presented a higher frequency of NaN when compared to the CO column data.
3.1. CO and CH4 Emission: Spatial Distribution
3.1.1. Monchique Wildfire, 2018
The Monchique wildfire is estimated to have burned 27,154 ha, of which shrubs and eucalyptus comprised 35% and cork oak forest 15%. Additionally, according to the in situ reports, the Monchique wildfire pointed to considerable irregularity in the expansion of the burned area, characterized by rapid fire spread due to plant formations prone to rapid and intense combustion (eucalyptus and shrubs, cork oak with abundant shrub development). In fact, in this particular wildfire, the meteorological and vegetation contexts favored the development of the Monchique fire due to the combination of strong winds, low relative humidity, and thin dead fuel. Thus, for the analysis of both CO and CH
4 emissions, a matrix of 77 × 77 km
2 was attained.
Figure 3 shows the spatial distribution of the total CO column retrievals (sum of partial columns) between 3 August and 9 August 2018. Throughout the analysis of the XCH
4 total retrievals (sum of partial columns), no relevant spatial distribution was found. Thus, for this fire event, the XCH
4 data was not shown since it presented several NaN results due to acquisition errors. In that regard, it may be noted that the presence of radiometric artefacts may be a contributor to spectral errors arising from the spatially heterogeneous nature of the radiance emanating from the Earth’s surface (due to irregular cloud cover, e.g., intense smoke plumes or albedo variations within a spatial sample) [
38].
The wildfire began on 3 August 2018, burning 325 ha. It is possible to observe in
Figure 3 that the higher intensities of CO column were located predominantly to the west, as confirmed by the in situ data [
26]. The largest expansion of the fire occurred at the end of 5 August, with two fire fronts corresponding to 31.6% of the total burned area (8587 ha) [
26]. As S5-P TROPOMI covered this region around 12:00 a.m. and 1:30 p.m. every day (small variations depending on the day), the 5 August large fire expansion was not recorded in the data shown in
Figure 3 for this day. It should be noted that the intensity of the flame front depends on the speed of propagation and the fuel load consumed in the propagation. The most severe phase of the fire occurred on 6 and 7 August [
26]. The evolution of the fire may also be explained through its radiative power (for detailed information, please see the Monchique Independent Technical Observatory report [
26]). Through the analysis of each day, the fire was seen to be almost inactive on the mornings of 4 and 5 August, which is in line with the distribution illustrated in
Figure 3 for these days. The highest peaks of radiative power were observed at the end of the day on 5 August [
26] (not recorded by the S5P-TROPOMI) and in the early afternoon of 7 and 8 August, with values of up to 700 MW (recorded by the S5P-TROPOMI). These fire behaviors are visible in
Figure 3. Thus, the uppermost CO columns measured were in the average of 5.82 × 10
18 ± 2.47 × 10
18 molecules/cm
2 (attained on 3, 6 and 7 August in different geographic coordinates).
3.1.2. Vila de Rei/Mação Wildfire, 2019
The total burned area estimated in the Vila de Rei/Mação wildfire was 9249 ha, in which 6881 ha were forest stands, 1862 ha shrubs, and 506 ha agricultural areas.
Figure 4 shows the spatial distribution profile of the CO column and XCH
4 total retrievals (sum of partial columns) between 20 July and 23 July 2019, where the largest plume of CO was observed on 21 July 2019 (up to 4.6 × 10
18 molecules/cm
2).
In the Vila de Rei/Mação wildfire the direction of the wind was highly unstable, as may also be observed in the spatial distribution of both the CO column and XCH
4 in
Figure 4. During this wildfire, the wind varied temporally and spatially in its speed and direction [
27]. These different wind patterns may justify the unusual forms of dispersion of the smoke plumes presented in
Figure 4, from the Vila de Rei/Mação wildfire during the afternoon of 20 July and the unclear distribution provided by S5-P TROPOMI both for CO column (20 and 23 July) and XCH
4 (20 and 23 July).
Moreover, the temperature fluctuations that occurred in this fire event may have screened critical instabilities in remote measurements [
39] (observed on 23 July for the CO column and XCH
4,
Figure 4). Furthermore, analyzing the fire radiation power data presented in the Vila de Rei Independent Technical Observatory report [
27], it was concluded that it is in line with the spatial distribution presented in
Figure 4a (presented for 21 July), where a sharp increase in the energy of the fire (up to 850 MW) was observed. Additionally, as observed in
Figure 4, the radiative power reached almost zero on 23 July.
It is clear by observation of
Figure 4 that the fuel, and therefore the characteristics of the forest’s vegetation, were critical for clear monitoring measurements of the CO column and XCH
4. The high quantity of smoke observed for this fire may have decreased the capacity of S5-P TROPOMI to draw a robust and clear spatial distribution of these gas emissions and follow the path of the wildfire. Nevertheless, for 21 July it was possible to pinpoint the highest peaks of CO emissions, contrary to CH
4 measurements. The measurements of the CH
4 emissions, a gas with low density when compared to CO, appeared to be greatly affected by the wind direction and intensity, moving away according to the wind’s behavior. Additionally, it should be noted that the most observed XCH
4 NaN readings ranged from 1853 ppb to 1862 ppb.
3.2. Combustion and Fuel Types: CO and CH4 Emission Trends
CO and CH
4 fluctuations during wildfires are complex and difficult to explain, and even more complicated in the case of wildland fuels such as wood, blades of grass, and tree leaves. These types of fuels will consequently affect the type of combustion profile. Wildfires can be broadly divided into two types: smoldering (heterogeneous combustion) and flaming (homogeneous combustion) [
40]. Both are important in wildfires, and despite being fundamentally different, one can lead to the other [
40]. These different types of combustion vary in their rates of spread, heat release, and gas emissions. In particular, CO and CH
4 emissions during a wildfire vary according to the type and quantity of fuel consumed, fuel moisture, ignition pattern, wind, temperature, and other factors. Flaming combustion results from a rapid oxidation reaction at high temperatures with an abundant oxygen supply, resulting in the release of carbon dioxide and water vapor [
40]. Smoldering combustion is a non-flaming form of combustion recognized by an abundant production of smoke with large quantities of particulate matter (mostly carbon) and carbon monoxide [
41]. The type of vegetation will influence the type of combustion during a wildfire, and therefore variation in the emissions of detected CO and CH
4.
Figure 5 shows the CO column and XCH
4 trend prior to, during, and following the wildfires under study (for full geo-localization the geographic location maps for both fires are in
Figures S6 and S7 in the supplementary data). The geographic coordinates presented in
Figure 5 are related to the CO column and XCH
4 peaks considered the highest and lowest emissions observed during all the days studied for both fire events. In
Figure 5, a linear interpolation was performed to overcome the missing data points due to S5-P TROPOMI acquisition errors.
Regarding the Monchique wildfire, the in situ data stated that not only wind speed explained the fire propagation, with a proportion of 53%, but also the humidity of the dead fuel (28%), associated with the relative humidity of the air and type of vegetation (19%). The graph (a.1) clearly shows that prior to and following the forest fire the emission of CO remained steady and between 6 August and 7 August, this CO emission plummeted dramatically to a further 34% when comparing both days. The XCH
4 in the atmosphere in pre-and post-moments was slightly lower compared to the highest emission (
Figure 5(b1) day and did not present an evident increment as in the CO column trend. In fact, even though the CH
4 emissions stabilized in 1999 [
42], this gas has been on the increase since 2007 for essentially unknown reasons [
43]. Furthermore, an in-depth discussion may be warranted due to the fact that according to the in situ data provided, during the first two days (3 and 4 August) the fire mainly affected eucalyptus (55% of the burned area) and other forest (29%) and its spread was not particularly rapid, possibly due to the defense of young eucalyptus stains. The largest expansion of the fire occurred on 5 August, having affected eucalyptus in around 50% of the burned area during that period. On 6 and 7 August, the burned shrub area (41% of the total) gained ground compared to the eucalyptus (44%) [
26]. These types of fuels (shrub) typically result in smoldering combustion, which is characterized by higher emissions of incomplete combustion products, including CO and CH
4. On 8 August, the fire essentially consumed areas of shrubs (70%). On 9 August, the coniferous species, the most representative of which is the pine species, recorded a reduced burned area. Both days revealed flaming combustion, which is more efficient than smoldering combustion, emitting lower quantities of CO and CH
4.
On the other hand, the fire fuel of Vila de Rei/Mação was mainly constituted by forest stands (60% maritime pine and 15% eucalyptus) and 20% shrub areas and small agricultural patches. According to the analysis of the in situ data [
27], the fuel mainly consisted of old wood or stands resulting from natural regeneration and with no forest management, with an average height of 2 m, high horizontal and vertical continuity, and a high load containing a significant quantity of fine suspended dead material. Thus, the behavior of the fire was expected to present a high speed of propagation and intensity. As far as
Figure 5(a2) is concerned, comparing the CO column trend prior to, during, and following the wildfire, the peak in CO column is evident, which decreased on day 23 and gradually adjusted to typical CO emission values for non-fire days. Regarding XCH
4, there were some days with data acquisition errors, probably caused by wind direction instability and high smoke intensity, which enabled the ability of S5-P TROPOMI to consistently measure XCH
4 emissions. Smoke intensity is also related to the humidity of the dead fine fuels. Considering the in situ data and using the physical model of Anderson et al. [
44], which estimates the moisture of the dead fine fuels, from 20 to 23 August, a relative humidity of between 20% and 40% in the mid-afternoon to a maximum of around 90% during the night was recorded. Thus, minimum and maximum values corresponding to the moisture content of the fine fuels standing at approximately 7.5% and 20% were obtained, which may have affected the quantity of smoke emitted during this period.
It is also important to establish the relationship between the CO column and XCH
4 S5-P TROPOMI data, as these two gases are related to wildfire emissions with incomplete combustion and they are expected to have an upward trend during the fire and a downward, steady profile pre- and post-fire. To understand this relationship, a linear regression was performed for the data, which is presented in
Figure 5.
Figure 6 presents a line fit plot for 95% of the confidence level between the CO column and XCH
4 S5-P TROPOMI data.
Analyzing the regression, the CO column and XCH4 distributions were moderately correlated, with a correlation coefficient of 0.66 (18 mutual observations) for the Monchique fire and 0.42 (10 mutual observations) for the Vila de Rei/Mação fire. It should be noted that these correlations were primarily limited by the few days of analysis and missing measurement files, mostly in the Vila de Rei/Mação fire. From the regression analysis, profiles and trends may be observed, and CO, as expected, had a higher expression in the emission when an extreme wildfire occurred compared to XCH4.
3.3. Spatio-Temporal Analysis of CO Emission
To assess the performance of S5-P TROPOMI, a quantitative analysis was carried out to evaluate the association of CO emissions with the actively burning areas according to the propagation maps (
Figures S3 and S4 in the supplementary data).
Figure 7 shows the squared 77 × 77 km
2 (centered at lat. 37°17′55.644″ N, long. 8°30′35.064″ W) for the Monchique wildfire for the most significant days recorded by S5-P TROPOMI (6, 7, 8, and 9 August), indicating the area of active burning. A statistical comparison of the CO column data in the cells with active burning and those of the surrounding background is shown with ANOVA tables and a graphical display.
As previously mentioned, high wind speed was observed on 6, 7, and 8 August with an evident northwest-southwest direction, as validated by the more intense CO plume for the higher CO emissions (darker red squares,
Figure 7a). According to the ANOVA tables and plots in
Figure 7b, it is possible to conclude that the CO columns measured by the S5P-TROPOMI were significantly higher over cells with active burning, especially on 6 and 7 August, but also on 8 August, with
p < 0.000 (high level of significance). It may also be noted that as on 9 August the fire was almost extinct, the burning areas and the surrounding background were similar in terms of CO emissions, showing (as in
Figure 4) that the CO plume was more diffuse and presented low values on that day. It may be concluded that there was a strong and statistically significant influence of the wildfire on the CO emissions measured by S5-P TROPOMI, as the remarkable decrease and increase when burning and background areas were compared were evident.
Figure 8, referring to 21 July, the most representative CO emissions day for the Vila de Rei/Mação wildfire, shows the assimilated observations for CO dynamics for this day.
Figure 8 shows the high representativeness of S5-P TROPOMI measurements for each in situ observation in the burned area of 21 July (centered at lat. 39°45′5.688″ N, long. 8°3′26.172″ W), which presented a
p-value of < 0.000 (high level of significance) when burning areas and the surrounding background were compared according to CO emission levels. As is also observed in
Figure 7, for the Monchique wildfire, the wind orientation influenced the CO plume. In the Vila de Rei/Mação wildfire, the wind orientation was unstable; nevertheless, the moderate westerly and southwesterly winds were dominant, as may be noted with the more intense red color in
Figure 8a.
This spatial and/or temporal cross-validation made possible the quantitative evaluation of the changing patterns of CO columns measured by S5-P TROPOMI. The spatial and/or temporal analysis described in
Figure 7 and
Figure 8, which consider the link between in situ observations and S5-P TROPOMI CO measurements, was a crucial step to accurately infer the potential of monitoring CO emissions during an extreme wildfire, using satellite data time series.
3.4. CO2 Emissions
In addition to the significance of CO emissions by means of the S5-P TROPOMI data, it was also relevant to predict the quantity of carbon dioxide (CO
2) emitted by the two fires under study, since it is known that climate change and, consequently, its associated wildfires are expected to increase atmospheric CO
2 [
45]. Considering that combustion is never 100% complete in vegetation fires, the potential of Equation (1), proposed by Drysdale [
32] and Ward et al. [
33], was explored.
Table 2 presents the predicted CO
2 concerning CO column data provided by S5-P TROPOMI, considering that the MCE yield values for wildland fires with smoldering and flaming combustion ranged between 0.75 and 0.92.
As previously mentioned, smoldering combustion is less efficient than flaming combustion and results in lower emissions of carbon dioxide (CO
2), but higher emissions of CO and CH
4 [
46]. On 7 August, in the Monchique wildfire, an estimated CO
2 quantity of 7.6 × 10
19 molecules/cm
2 was emitted, considering 92% combustion efficiency, in an area of 7 × 7 km
2 for each geolocation. Regarding the Vila de Rei/Mação wildfire, the higher emission of predicted CO
2 revealed up to 1.4 × 10
19 molecules/cm
2 when 75% combustion efficiency was considered and 5.3 × 10
19 molecules/cm
2 considering 92% combustion efficiency. When the uppermost peaks of CO
2 were compared to other research articles, the estimated emissions were higher according to the values found by Al-Saadi et al. [
47], who reported 4.4 × 10
17 molecules/cm
2 of CO emission for biomass burning, and therefore, for both 92% and 75% combustion efficiency, a CO
2 emission was estimated to record an average of 4.9 × 10
18 or 1.3 × 10
18 molecules/cm
2, respectively. Conversely, close to the Senegal region, Buchwitz et al. [
48] monitored a CO
2 emission plume of 8.1 × 10
21 molecules/cm
2, showing that CO
2 emissions are also highly dependent on the burned area estimation, in particular for short-lived wildfires [
48]. The CO
2 emissions present high spatial heterogeneity, since they will be highly dependent on the fuel and weather conditions [
7].
4. Conclusions and Final Remarks
In this study, the potential of the S5-P TROPOMI satellite for the monitoring and supervision of CO and CH4 during wildfire events was assessed to analyze Level-2 data products and their correspondence with in situ data for two particular Portuguese extreme wildfires: Monchique in 2018 and Vila de Rei/Mação in 2019.
From the spatial distribution profiles created for the CO column and XCH4 emissions through the S5-P TROPOMI Level-2 data, it was concluded that, firstly, the in situ data is key to the construction of a more in-depth understanding of the patterns of these two gases during an extreme wildfire event.
Secondly, when comparing the robustness of S5-P TROPOMI for both gases, the CO column measurements presented a clear trend, patterns, and evident distribution, in line with the fire behavior and intensity. On the contrary, for XCH4 measurements, it was not possible to explain the fire direction, only the intensified emission when the fire occurred. In the XCH4 measurements, NaN results were mostly found in up to 1853 ppb, together with the higher burning intensity during the wildfire event. It should also be noted that as CH4 is lighter than CO, the gas may be carried away with sea winds, therefore compromising its measurements. Consequently, the wind and smoke plumes may be contributing factors in spectral errors, namely for XCH4 measurements.
Thirdly, it was concluded that S5-P TROPOMI’s potential for screening CO fluctuations during a fire event (namely, Pinus pinaster and Eucalyptus globulus burning fuel) is highly affected by the type of forest fire under study. For the Monchique fire, in CO column measurements, as the wildfire formed loft smoke plumes above the boundary layer and promoted the long-distance transport of gases and particulate matter, the S5-P TROPOMI was able not only to sense fluctuations in the emissions’ trends but also to monitor the direction of the fire’s propagation. However, for Vila de Rei/Mação, due to high wind instability, the smoke aerosols remained in the near-ground layer and were not sufficiently high to enable S5-P TROPOMI to clearly follow the CO direction in the last two days of the fire event.
Fourthly, by means of a spatio-temporal analysis, the quantitative influence of the fire events on CO emissions correlated with burned propagation maps, showing with a significant difference that S5-P TROPOMI was able to provide prospects in assessing and quantifying the CO columns during wildfire events. This analysis corroborates the data found in the qualitative and descriptive analysis.
Thus, it is important to highlight that S5-P TROPOMI’s potential for screening patterns and CO columns, contrary to XCH4 monitoring, which may be ambiguous, can provide a wealth of knowledge on mapping wildfire events.