skip to main content


Search for: All records

Award ID contains: 1831013

Note: When clicking on a Digital Object Identifier (DOI) number, you will be taken to an external site maintained by the publisher. Some full text articles may not yet be available without a charge during the embargo (administrative interval).
What is a DOI Number?

Some links on this page may take you to non-federal websites. Their policies may differ from this site.

  1. Abstract

    Emission factors (EFs) are crucial in understanding the effects of wildfire emissions on air quality. We examined the variability of EFs of three wildfires (Nethker, Castle, and 204 Cow) during the 2019 Western US wildfire season using the Aerodyne Mobile Laboratory (AML) and compared them to previous studies. The AML sampling captured the high degree of variability present in wildfires, and we report results for a range of combustion conditions that is more extensive than previous field and laboratory studies. For instance, we captured emissions from freshly started flaming fuels and we report rare EF measurements at very high modified combustion efficiencies (MCEs); MCEs >0.9. Differences in emissions between AML‐observed wildfires were attributed to burning state/MCE rather than fuel type. A comparison of EFs versus MCE was made and linear fits were compared to previous observations to reveal important differences that incorporate these high MCEs. For some species, there remains an EF dependence on MCE at these high values, while others reach a minimum value and exhibit either no or a weak dependence above it. EF differences were found for many of the studied compounds when comparing ground‐based and airborne observations, with generally greater airborne EFs possibly due to photochemical oxidation. The largest differences were from monoterpenes and acetaldehyde. Comparisons were made between AML‐observed wildfires, aircraft observations, and the values in literature for EFs and emission ratios, with mixed agreement due to the high degree of variability caused by differences in MCE. Differences in MCE drove the diurnal EF differences.

     
    more » « less
  2. Abstract

    Long‐term exposure to ambient fine particulate matter (PM2.5) is the second leading risk factor of premature death in Sub‐Saharan Africa. We use GEOS‐Chem to quantify the effects of (a) trash burning, (b) residential solid‐fuel burning, and (c) open biomass burning (BB) (i.e., landscape fires) on ambient PM2.5and PM2.5‐attributable mortality in Africa. Using a series of sensitivity simulations, we excluded each of the three combustion sources in each of five African regions. We estimate that in 2017 emissions from these three combustion sources within Africa increased global ambient PM2.5by 2%, leading to 203,000 (95% confidence interval: 133,000–259,000) premature mortalities yr−1globally and 167,000 premature mortalities yr−1in Africa. BB contributes more ambient PM2.5‐related premature mortalities per year (63%) than residential solid‐fuel burning (29%) and trash burning (8%). Open BB in Central Africa leads to the largest number of PM2.5‐attributed mortalities inside the region, while trash burning in North Africa and residential solid‐fuel burning in West Africa contribute the most regional mortalities for each source. Overall, Africa has a unique ambient air pollution profile because natural sources, such as windblown dust and BB, contribute strongly to ambient PM2.5levels and PM2.5‐related mortality. Air pollution policies may need to focus on taking preventative measures to avoid exposure to ambient PM2.5from these less‐controllable sources.

     
    more » « less
  3. null (Ed.)
  4. null (Ed.)
  5. null (Ed.)
    Abstract. There are many fuels used for domestic purposes in east Africa, producing a significant atmospheric burden of the resulting aerosols, which includes biomass burning particles. However, the aerosol physicochemical properties are poorly understood. Here, the combustion of eucalyptus, acacia, and olive fuels was performed at 500 and 800 ∘C in a tube furnace, followed by immediate filter collection for fresh samples or introduction into a photochemical chamber to simulate atmospheric photochemical aging under the influence of anthropogenic emissions. The aerosol generated in the latter experiment was collected onto filters after 12 h of photochemical aging. 500 and 800 ∘C were selected to simulate smoldering and flaming combustion, respectively, and to cover a range of combustion conditions. Methanol extracts from Teflon filters were analyzed by ultra-performance liquid chromatography interfaced to both a diode array detector and an electrospray ionization high-resolution quadrupole time-of-flight mass spectrometer (UPLC/DAD-ESI-HR-QTOFMS) to determine the light absorption properties of biomass burning organic aerosol constituents chemically characterized at the molecular level. Few chemical or UV–visible (UV: ultraviolet) differences were apparent between samples for the fuels when combusted at 800 ∘C. Differences in single-scattering albedo (SSA) between fresh samples at this temperature were attributed to compounds not captured in this analysis, with eucalyptol being one suspected missing component. For fresh combustion at 500 ∘C, many species were present; lignin pyrolysis and distillation products are more prevalent in eucalyptus, while pyrolysis products of cellulose and at least one nitro-aromatic species were more prevalent in acacia. SSA trends areconsistent with this, particularly if the absorption of those chromophoresextends to the 500–570 nm region. Upon aging, both show that resorcinolor catechol was removed to the highest degree, and both aerosol types weredominated by loss of pyrolysis and distillation products, though they differed in the specific compounds being consumed by the photochemical aging process. 
    more » « less
  6. null (Ed.)
    Biomass burning (BB) aerosols contribute to climate forcing, but much is still unknown about the extent of this forcing, owing partially to the high level of uncertainty regarding BB aerosol optical properties. A key optical parameter is the refractive index (RI), which influences the absorbing and scattering properties of aerosols. This quantity is not measured directly, but it is obtained by fitting the measured scattering cross section and extinction cross section to a theoretical model using the RI as a fitting parameter. We used the Rayleigh–Debye–Gans (RDG) approximation to retrieve the complex RI of freshly emitted BB aerosol from two fuels (eucalyptus and olive) from Africa in the spectral range of 500–580 nm. Experimental measurements were carried out using cavity ring-down spectroscopy to measure extinction over the range of wavelengths of 500–580 nm and nephelometry to measure scattering at three wavelengths of 450, 550, and 700 nm for size-selected BB aerosol particles. The fuels were combusted in a tube furnace at a temperature of 800 °C, which is representative of the flaming stage of burning. Filter samples were collected and imaged using tunneling electron microscopy to obtain information on the morphology and size of the particles, which was used in the RDG calculations. The mean radii of the monomers were 27.8 and 31.5 nm for the eucalyptus and the olive fuels, respectively. The components of the retrieved complex RI were in the range of 1.31 ≤ n ≤ 1.56 and 0.045 ≤ k ≤ 0.468. The real and complex parts of the RI increase with increasing particle mobility diameter. The real part of the RI is lower, and the imaginary part is higher than what was recommended in literature for black carbon generated by propane or field measurements from fires of mixed wood samples. Fuel dependent results from controlled laboratory experiments can be used in climate modeling efforts and to constrain field measurements from biomass burning. 
    more » « less
  7. null (Ed.)
    Abstract. An accurate measurement of the optical properties of aerosol is critical for quantifying the effect of aerosol on climate. Uncertainties persist and results of measurements vary significantly. Biomass burning (BB) aerosol has been extensively studied through both field and laboratory environments for North American fuels to understand the changes in opticaland chemical properties as a function of aging. There is a need for a widersampling of fuels from different regions of the world for laboratory studies. This work represents the first such study of the optical andchemical properties of wood fuel samples commonly used for domestic purposes ineast Africa. In general, combustion temperature or modified combustionefficiency (MCE) plays a major role in the optical properties of the emitted aerosol. For fuels combusted with MCE of 0.974±0.015, which is referred to as flaming-dominated combustion, the single-scattering albedo (SSA) values were in the range of 0.287 to 0.439, while for fuels combusted with MCE of 0.878±0.008, which is referred to as smoldering-dominated combustion, the SSA values were in the range of 0.66 to 0.769. There is a clear but very small dependence of SSA on fuel type. A significant increase in the scattering and extinction cross section (with no significant change inabsorption cross section) was observed, indicating the occurrence of chemistry, even during dark aging for smoldering-dominated combustion. Thisfact cannot be explained by heterogeneous oxidation in the particle phase,and we hypothesize that secondary organic aerosol formation is potentiallyhappening during dark aging. After 12 h of photochemical aging, BB aerosolbecomes highly scattering with SSA values above 0.9, which can be attributedto oxidation in the chamber. Aging studies of aerosol from flaming-dominatedcombustion were inconclusive due to the very low aerosol number concentration. We also attempted to simulate polluted urban environments byinjecting volatile organic compounds (VOCs) and BB aerosol into the chamber, but no distinct difference was observed when compared to photochemical aging in the absence of VOCs. 
    more » « less