Debora Griffin

Dr. Debora Griffin

Air Quality Research Division, Environment and Climate Change Canada
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Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 January 2019 in Geophysical Research Letters
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DGDebora Griffin
Debora Griffin
XZXiaoyi Zhao
Xiaoyi Zhao
CMChris McLinden
Chris McLinden
FBFolkert Boersma
Folkert Boersma
ABAdam Bourassa
Adam Bourassa
MWMengistu Wolde
Mengistu Wolde
TROPOspheric Monitoring Instrument (TROPOMI), on‐board the Sentinel‐5 Precurser satellite, is a nadir‐viewing spectrometer measuring reflected sunlight in the ultraviolet, visible, near‐infrared, and shortwave infrared. From these spectra several important air quality and climate‐related atmospheric constituents are retrieved, including nitrogen dioxide (NO2) at unprecedented spatial resolution from a satellite platform. We present the first retrievals of TROPOMI NO2 over the Canadian Oil Sands, contrasting them with observations from the Ozone Monitoring Instrument satellite instrument, and demonstrate TROPOMI's ability to resolve individual plumes and highlight its potential for deriving emissions from individual mining facilities. Further, the first TROPOMI NO2 validation is presented, consisting of aircraft and surface in situ NO2 observations, and ground‐based remote‐sensing measurements between March and May 2018. Our comparisons show that the TROPOMI NO2 vertical column densities are highly correlated with the aircraft and surface in situ NO2 observations, and the ground‐based remote‐sensing measurements with a low bias (15–30 %); this bias can be reduced by improved air mass factors.

5 September 2020 in Geophysical Research Letters
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DGDaniel Goldberg
Daniel Goldberg
SASusan C. Anenberg
Susan C. Anenberg
DGDebora Griffin
Debora Griffin
CMChris McLinden
Chris McLinden
ZLZifeng Lu
Zifeng Lu
DSDavid G. Streets
David G. Streets
TROPOMI satellite data show substantial drops in nitrogen dioxide (NO2) during COVID‐19 physical distancing. To attribute NO2 changes to NOx emissions changes over short timescales, one must account for meteorology. We find that meteorological patterns were especially favorable for low NO2 in much of the United States in spring 2020, complicating comparisons with spring 2019. Meteorological variations between years can cause column NO2 differences of ~15% over monthly timescales. After accounting for solar angle and meteorological considerations, we calculate that NO2 drops ranged between 9.2% and 43.4% among 20 cities in North America, with a median of 21.6%. Of the studied cities, largest NO2 drops (>30%) were in San Jose, Los Angeles, and Toronto, and smallest drops (<12%) were in Miami, Minneapolis, and Dallas. These normalized NO2 changes can be used to highlight locations with greater activity changes and better understand the sources contributing to adverse air quality in each city.

2 October 2019 in Atmospheric Chemistry and Physics
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EDEnrico Dammers
Enrico Dammers
CMChris McLinden
Chris McLinden
DGDebora Griffin
Debora Griffin
MSMark W. Shephard
Mark W. Shephard
SGShelley Van Der Graaf
Shelley Van Der Graaf
JEJan Willem Erisman
Jan Willem Erisman
Ammonia (NH3) is an essential reactive nitrogen species in the biosphere and through its use in agriculture in the form of fertilizer (important for sustaining humankind). The current emission levels, however, are up to 4 times higher than in the previous century and continue to grow with uncertain consequences to human health and the environment. While NH3 at its current levels is a hazard to environmental and human health, the atmospheric budget is still highly uncertain, which is a product of an overall lack of measurements. The capability to measure NH3 with satellites has opened up new ways to study the atmospheric NH3 budget. In this study, we present the first estimates of NH3 emissions, lifetimes and plume widths from large (>∼5 kt yr−1) agricultural and industrial point sources from Cross-track Infrared Sounder (CrIS) satellite observations across the globe with a consistent methodology. The same methodology is also applied to the Infrared Atmospheric Sounding Interferometer (IASI) (A and B) satellite observations, and we show that the satellites typically provide comparable results that are within the uncertainty of the estimates. The computed NH3 lifetime for large point sources is on average 2.35±1.16 h. For the 249 sources with emission levels detectable by the CrIS satellite, there are currently 55 locations missing (or underestimated by more than an order of magnitude) from the current Hemispheric Transport Atmospheric Pollution version 2 (HTAPv2) emission inventory and only 72 locations with emissions within a factor of 2 compared to the inventories. The CrIS emission estimates give a total of 5622 kt yr−1, for the sources analyzed in this study, which is around a factor of ∼2.5 higher than the emissions reported in HTAPv2. Furthermore, the study shows that it is possible to accurately detect short- and long-term changes in emissions, demonstrating the possibility of using satellite-observed NH3 to constrain emission inventories.

2 October 2019 in Atmospheric Measurement Techniques
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KGKaterina Garane
Katerina Garane
MKMaria-Elissavet Koukouli
Maria-Elissavet Koukouli
TVTijl Verhoelst
Tijl Verhoelst
CLChristophe Lerot
Christophe Lerot
KHKlaus-Peter Heue
Klaus-Peter Heue
WZWalter Zimmer
Walter Zimmer
In October 2017, the Sentinel-5 Precursor (S5P) mission was launched, carrying the TROPOspheric Monitoring Instrument (TROPOMI), which provides a daily global coverage at a spatial resolution as high as 7 km × 3.5 km and is expected to extend the European atmospheric composition record initiated with GOME/ERS-2 in 1995, enhancing our scientific knowledge of atmospheric processes with its unprecedented spatial resolution. Due to the ongoing need to understand and monitor the recovery of the ozone layer, as well as the evolution of tropospheric pollution, total ozone remains one of the leading species of interest during this mission. In this work, the TROPOMI near real time (NRTI) and offline (OFFL) total ozone column (TOC) products are presented and compared to daily ground-based quality-assured Brewer and Dobson TOC measurements deposited in the World Ozone and Ultraviolet Radiation Data Centre (WOUDC). Additional comparisons to individual Brewer measurements from the Canadian Brewer Network and the European Brewer Network (Eubrewnet) are performed. Furthermore, twilight zenith-sky measurements obtained with ZSL-DOAS (Zenith Scattered Light Differential Optical Absorption Spectroscopy) instruments, which form part of the SAOZ network (Système d'Analyse par Observation Zénitale), are used for the validation. The quality of the TROPOMI TOC data is evaluated in terms of the influence of location, solar zenith angle, viewing angle, season, effective temperature, surface albedo and clouds. For this purpose, globally distributed ground-based measurements have been utilized as the background truth. The overall statistical analysis of the global comparison shows that the mean bias and the mean standard deviation of the percentage difference between TROPOMI and ground-based TOC is within 0 –1.5 % and 2.5 %–4.5 %, respectively. The mean bias that results from the comparisons is well within the S5P product requirements, while the mean standard deviation is very close to those limits, especially considering that the statistics shown here originate both from the satellite and the ground-based measurements. Additionally, the TROPOMI OFFL and NRTI products are evaluated against already known spaceborne sensors, namely, the Ozone Mapping Profiler Suite, on board the Suomi National Polar-orbiting Partnership (OMPS/Suomi-NPP), NASA v2 TOCs, and the Global Ozone Monitoring Experiment 2 (GOME-2), on board the Metop-A (GOME-2/Metop-A) and Metop-B (GOME-2/Metop-B) satellites. This analysis shows a very good agreement for both TROPOMI products with well-established instruments, with the absolute differences in mean bias and mean standard deviation being below +0.7 % and 1 %, respectively. These results assure the scientific community of the good quality of the TROPOMI TOC products during its first year of operation and enhance the already prevalent expectation that TROPOMI/S5P will play a very significant role in the continuity of ozone monitoring from space.

20 January 2023 in Journal of Geophysical Research: Atmospheres
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CWCarsten Warneke
Carsten Warneke
JSJoshua Schwarz
Joshua Schwarz
JDJack Dibb
Jack Dibb
OKOlga Kalashnikova
Olga Kalashnikova
GFGregory Frost
Gregory Frost
TTThe FIREX‐AQ Science Team
The FIREX‐AQ Science Team
The NOAA/NASA Fire Influence on Regional to Global Environments and Air Quality (FIREX‐AQ) experiment was a multi‐agency, inter‐disciplinary research effort to: (a) obtain detailed measurements of trace gas and aerosol emissions from wildfires and prescribed fires using aircraft, satellites and ground‐based instruments, (b) make extensive suborbital remote sensing measurements of fire dynamics, (c) assess local, regional, and global modeling of fires, and (d) strengthen connections to observables on the ground such as fuels and fuel consumption and satellite products such as burned area and fire radiative power. From Boise, ID western wildfires were studied with the NASA DC‐8 and two NOAA Twin Otter aircraft. The high‐altitude NASA ER‐2 was deployed from Palmdale, CA to observe some of these fires in conjunction with satellite overpasses and the other aircraft. Further research was conducted on three mobile laboratories and ground sites, and 17 different modeling forecast and analyses products for fire, fuels and air quality and climate implications. From Salina, KS the DC‐8 investigated 87 smaller fires in the Southeast with remote and in‐situ data collection. Sampling by all platforms was designed to measure emissions of trace gases and aerosols with multiple transects to capture the chemical transformation of these emissions and perform remote sensing observations of fire and smoke plumes under day and night conditions. The emissions were linked to fuels consumed and fire radiative power using orbital and suborbital remote sensing observations collected during overflights of the fires and smoke plumes and ground sampling of fuels.

26 February 2020 in Atmospheric Chemistry and Physics
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MSMark W. Shephard
Mark W. Shephard
EDEnrico Dammers
Enrico Dammers
KCKaren E. Cady-Pereira
Karen E. Cady-Pereira
SKShailesh K. Kharol
Shailesh K. Kharol
JTJesse Thompson
Jesse Thompson
QZQiong Zheng
Qiong Zheng
Despite its clear importance, the monitoring of atmospheric ammonia, including its sources, sinks, and links to the greater nitrogen cycle, remains limited. Satellite data are helping to fill the gap in monitoring from sporadic conventional ground- and aircraft-based observations to better inform policymakers and assess the impact of any ammonia-related policies. Presented is a description and survey that demonstrate the capabilities of the Cross-track Infrared Sounder (CrIS) ammonia product for monitoring, air quality forecast model evaluation, dry deposition estimates, and emission estimates from an agricultural hotspot. For model evaluation, while there is a general agreement in the spatial allocation of known major agricultural ammonia hotspots across North America, the satellite observations show some high-latitude regions during peak forest fire activity often have ammonia concentrations approaching those in agricultural hotspots. The CrIS annual ammonia dry depositions in Canada (excluding the territories) and the US have average and annual variability values of ∼0.8±0.08 and ∼1.23±0.09 Tg N yr−1, respectively. These satellite-derived dry depositions of reactive nitrogen from NH3 with NO2 show an annual ratio of NH3 compared to their sum (NH3+NO2) of ∼82 % and ∼55 % in Canada and the US, respectively. Furthermore, we show the use of CrIS satellite observations to estimate annual and seasonal emissions near Lethbridge, Alberta, Canada, a region dominated by high-emission concentrated animal feeding operations (CAFOs); the satellite annual emission estimate of 37.1±6.3 kt yr−1 is at least double the value reported in current bottom-up emission inventories for this region.