Air pollution associated with wildfire smoke transport during the summer can significantly affect ozone (O3) and particulate matter (PM) concentrations, even in heavily populated areas like New York ...City (NYC). Here, we use observations from aircraft, ground-based lidar, in-situ analyzers and satellite to study and assess wildfire smoke transport, vertical distribution, optical properties, and potential impact on air quality in the NYC urban and coastal areas during the summer 2018 Long Island Sound Tropospheric Ozone Study (LISTOS). We investigate an episode of dense smoke transported and mixed into the planetary boundary layer (PBL) on August 15–17, 2018. The horizontal advection of the smoke is shown to be characterized with the prevailing northwest winds in the PBL (velocity > 10 m/s) based on Doppler wind lidar measurements. The wildfire sources and smoke transport paths from the northwest US/Canada to northeast US are identified from the NOAA hazard mapping system (HMS) fires and smoke product and NOAA-HYbrid Single Particle Lagrangian Integrated Trajectory (HYSPLIT) backward trajectory analysis. The smoke particles are distinguished from the urban aerosols by showing larger lidar-ratio (70-sr at 532-nm) and smaller depolarization ratio (0.02) at 1064-nm using the NASA High Altitude Lidar Observatory (HALO) airborne high-spectral resolution lidar (HSRL) measurements. The extinction-related angstrom exponents in the near-infrared (IR at 1020–1640 nm) and Ultraviolet (UV at 340–440 nm) from NASA-Aerosol Robotic Network (AERONET) product show a reverse variation trend along the smoke loadings, and their absolute differences indicate strong correlation with the smoke-Aerosol Optical Depth (AOD) (R > 0.94). We show that the aloft smoke plumes can contribute as much as 60–70% to the column AOD and that concurrent high-loadings of O3, carbon monoxide (CO), and black carbon (BC) were found in the elevated smoke layers from the University of Maryland (UMD) aircraft in-situ observations. Meanwhile, the surface PM2.5 (PM with diameter ≤ 2.5 μm), organic carbon (OC) and CO measurements show coincident and sharp increase (e.g., PM2.5 from 5 μg/m3 before the plume intrusion to ~30 μg/m3) with the onset of the plume intrusions into the PBL along with hourly O3 exceedances in the NYC region. We further evaluate the NOAA-National Air Quality Forecasting Capability (NAQFC) model PBL-height, PM2.5, and O3 with the observations and demonstrate good consistency near the ground during the convective PBL period, but significant bias at other times. The aloft smoke layers are sometimes missed by the model.
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•Characterize the wildfire smoke optical properties and mixing into PBL•Distinguish smoke particles and their mixture from urban aerosols•Demonstrate concurrent high-loadings of O3, CO and BC in the elevated smoke layers•Quantify dramatic impacts of transported smoke on the air quality in NYC area•Assess the NOAA-NAQFC modeling PBLH, PM2.5 and O3
Airborne differential absorption lidar (DIAL) offers a uniquely capable solution to the problem of measuring water vapor (WV) with high precision, accuracy, and resolution throughout the troposphere ...and lower stratosphere. The High Altitude Lidar Observatory (HALO) airborne WV DIAL was recently developed at NASA Langley Research Center and was first deployed in 2019. It uses four wavelengths near 935 nm to achieve sensitivity over a wide dynamic range and simultaneously employs 1064 nm backscatter and 532 nm high-spectral-resolution lidar (HSRL) measurements for aerosol and cloud profiling. A key component of the WV retrieval framework is flexibly trading resolution for precision to achieve optimal datasets for scientific objectives across scales. An approach to retrieving WV in the lowest few hundred meters of the atmosphere using the strong surface return signal is also presented.
The NASA Langley Research Center High Altitude Lidar Observatory (HALO) is a multi-functional and modular lidar developed to
address the observational needs of NASA's weather, climate, carbon cycle,
...and atmospheric composition focus areas. HALO measures atmospheric H2O
mixing ratios, CH4 mole fractions, and aerosol/cloud optical properties using the differential absorption lidar (DIAL) and high-spectral-resolution lidar (HSRL) techniques. In 2019 HALO participated in the NASA Atmospheric Carbon and Transport – America campaign on board the NASA C-130 to complement a suite of greenhouse gas in situ sensors and provide, for the first time, simultaneous measurements of column CH4 and aerosol/cloud profiles. HALO operated in 18 of 19 science flights where the DIAL and
integrated path differential absorption (IPDA) lidar techniques at 1645 nm were used for column and multi-layer measurements of CH4 mole fractions, and the HSRL and backscatter techniques were used at 532 and 1064 nm,
respectively, for retrievals of aerosol backscatter, extinction,
depolarization, and mixing layer heights. In this paper we present HALO's
measurement theory for the retrievals of column and multi-layer XCH4, retrieval accuracy, and precision including methods for bias correction and a comprehensive total column XCH4 validation comparison to in situ observations. Comparisons of HALO XCH4 to in situ-derived XCH4, collected during spiral ascents and descents, indicate a mean difference of 2.54 ppb and standard deviation (SD) of the differences of 16.66 ppb when employing 15 s along-track averaging (<3 km). A high correlation coefficient of R=0.9058 was observed for the 11 in situ spiral comparisons. Column XCH4 measured by HALO over regional scales covered by the ACT-America campaign is compared against in situ CH4 measurements carried out within the planetary boundary layer (PBL) from both the C-130 and B200 aircraft. Favorable correlation between the in situ point
measurements within the PBL and the remote column measurements from HALO
elucidates the sensitivity of a column-integrating lidar to CH4
variability within the PBL, where surface fluxes dominate the signal. Novel capabilities for CH4 profiling in regions of clear air using the DIAL technique are presented and validated for the first time. Additionally, profiling of CH4 is used to apportion the PBL absorption from the total column and is compared to previously reported IPDA cloud slicing techniques that estimate PBL columns using strong echoes from fair weather cumulus. The analysis presented here points towards HALO's ability to retrieve accurate and precise CH4 columns with the prospects for future multi-layer profiling in support of future suborbital campaigns.
The Lidar Atmospheric Sensing Experiment (LASE) on board the NASA DC-8 measured high-resolution profiles of water vapor and aerosols, and cloud distributions in 14 flights over the eastern North ...Atlantic during the NASA African Monsoon Multidisciplinary Analyses (NAMMA) field experiment. These measurements were used to study African easterly waves (AEWs), tropical cyclones (TCs), and the Saharan air layer (SAL). These LASE measurements represent the first simultaneous water vapor and aerosol lidar measurements to study the SAL and its interactions with AEWs and TCs. Three case studies were selected for detailed analysis: (i) a stratified SAL, with fine structure and layering (unlike a well-mixed SAL), (ii) a SAL with high relative humidity (RH), and (iii) an AEW surrounded by SAL dry air intrusions. Profile measurements of aerosol scattering ratios, aerosol extinction coefficients, aerosol optical thickness, water vapor mixing ratios, RH, and temperature are presented to illustrate their characteristics in the SAL, convection, and clear air regions. LASE extinction-to-backscatter ratios for the dust layers varied from 35 plus or minus 5 to 45 plus or minus 5 sr, well within the range of values determined by other lidar systems. LASE aerosol extinction and water vapor profiles are validated by comparison with onboard in situ aerosol measurements and GPS dropsonde water vapor soundings, respectively. An analysis of LASE data suggests that the SAL suppresses low-altitude convection. Midlevel convection associated with the AEW and transport are likely responsible for high water vapor content observed in the southern regions of the SAL on 20 August 2008. This interaction is responsible for the transfer of about 7 10 super(15) J (or 8 10 super(3) J m super(-2)) latent heat energy within a day to the SAL. Initial modeling studies that used LASE water vapor profiles show sensitivity to and improvements in model forecasts of an AEW.
Autotaxin (ATX, also known as ectonucleotide pyrophosphatase/phosphodiesterase-2, ENPP2) is a secreted lysophospholipase D that generates the lipid mediator lysophosphatidic acid (LPA), a mitogen and ...chemoattractant for many cell types. ATX-LPA signaling is involved in various pathologies including tumor progression and inflammation. However, the molecular basis of substrate recognition and catalysis by ATX and the mechanism by which it interacts with target cells are unclear. Here, we present the crystal structure of ATX, alone and in complex with a small-molecule inhibitor. We have identified a hydrophobic lipid-binding pocket and mapped key residues for catalysis and selection between nucleotide and phospholipid substrates. We have shown that ATX interacts with cell-surface integrins through its N-terminal somatomedin B-like domains, using an atypical mechanism. Our results define determinants of substrate discrimination by the ENPP family, suggest how ATX promotes localized LPA signaling and suggest new approaches for targeting ATX with small-molecule therapeutic agents.
In situ and laser remote measurements of gases and aerosols were made with airborne instrumentation to establish a baseline chemical signature of the atmosphere above the South Pacific Ocean during ...the NASA Global Tropospheric Experiment (GTE)/Pacific Exploratory Mission‐Tropics A (PEM‐Tropics A) conducted in August‐October 1996. This paper discusses general characteristics of the air masses encountered during this experiment using an airborne lidar system for measurements of the large‐scale variations in ozone (O3) and aerosol distributions across the troposphere, calculated potential vorticity (PV) from the European Centre for Medium‐Range Weather Forecasting (ECMWF), and in situ measurements for comprehensive air mass composition. Between 8°S and 52°S, biomass burning plumes containing elevated levels of O3, over 100 ppbv, were frequently encountered by the aircraft at altitudes ranging from 2 to 9 km. Air with elevated O3 was also observed remotely up to the tropopause, and these air masses were observed to have no enhanced aerosol loading. Frequently, these air masses had some enhanced PV associated with them, but not enough to explain the observed O3 levels. A relationship between PV and O3 was developed from cases of clearly defined O3 from stratospheric origin, and this relationship was used to estimate the stratospheric contribution to the air masses containing elevated O3 in the troposphere. The frequency of observation of the different air mass types and their average chemical composition is discussed in this paper.
The Lidar Atmospheric Sensing Experiment (LASE) was operated autonomously from the NASA high‐altitude ER‐2 aircraft on nine flights during July 10–26, 1996, as part of the Tropospheric Aerosol ...Radiative Forcing Observational Experiment (TARFOX). LASE measured high‐resolution profiles of water vapor and aerosols in regions of urban haze plumes over the U.S. eastern seaboard. Real‐time LASE aerosol measurements were used to guide the in situ aircraft to sample haze layers. In this paper the vertical and horizontal distributions of aerosol backscatter measured by LASE are presented along with the temporal evolution of the haze layers. The aerosol backscatter data also identify the presence of gradients in the aerosol plumes, the presence of low‐altitude clouds, and optically thin cirrus. This information is useful for many of the radiometeric observations made during TARFOX and can help explain observational differences among ground, airborne, and satellite observations. An iterative procedure is discussed which was used to invert lidar data to retrieve aerosol scattering ratios, extinction, and total optical depths from the LASE measurements. The sensitivity of these retrievals to assumed parameters is discussed and the results of retrievals are also compared to the well‐known Bernoulli method. LASE water vapor measurements were made across the entire troposphere using a three “line pair” method to cover the range of water vapor mixing ratio from < 0.01 g/kg near the tropopause to ∼ 20 g/kg near the surface in a single aircraft pass over the experiment region. These measurements also show two‐dimensional distributions of large spatial gradients in water vapor in the lower and upper troposphere. These observations are useful in the calculation of IR radiation fields and relative humidity fields, since relative humidity has a strong influence on the growth of aerosols and their scattering properties. Water vapor profiles, aerosol scattering ratios, aerosol extinction coefficients and aerosol optical depths were derived using the methodology presented in this paper from LASE measurements during TARFOX. These measurements are compared with other in situ and remote measurements during TARFOX in the companion papers Ferrare et al., this issue (a, b)
The NASA Langley UV differential absorption lidar (DIAL) system flew on the NASA DC‐8 aircraft during the Stratospheric Aerosol and Gas Experiment (SAGE) III Ozone Loss and Validation ...Experiment/Third European Stratospheric Experiment on Ozone 2000 (SOLVE/THESEO 2000) mission from 30 November 1999 to 15 March 2000. The UV DIAL system measured ozone (O3) profiles at altitudes from about 1 km above the aircraft up to about 26 km with a vertical resolution of 750 m and a horizontal resolution of 70 km below 19 km and 140 km above 19 km. In comparison with electrochemical concentration cell ozonesonde profiles, the UV DIAL O3 measurements agreed to within 5% up to 20 km and 10% from 20 to 25 km. Ozone loss during the season was determined using the UV DIAL O3 data along with air mass subsidence determined using N2O as a conservative tracer at five levels from 50 to 250 ppbv Greenblatt et al., 2002. O3 mixing ratios were determined inside the polar vortex, away from the collar region along these five levels during the mission. The maximum O3 loss determined from 30 November to 12 March was 1.55 ± 0.3 ppmv at the 440–450 K potential temperature (Θ) level, while the loss there between 20 January and 15 March was 1.3 ± 0.3 ppmv. These results are comparable to many of the other reported losses for these periods, but lower than several. Some of the determinations of higher losses used a different method to determine descent during the season. These results indicate that a series of vertical profiles of O3 that sample much of the vortex during the winter, along with determinations of the descent of air masses inside the vortex, can give a reasonable estimate of the O3 changes during the season.
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