Greenhouse effects of aircraft emissions as calculated by a radiative transfer model

1995 ◽  
Vol 13 (4) ◽  
pp. 413-418 ◽  
Author(s):  
J. P. F. Fortuin ◽  
R. van Dorland ◽  
W. M. F. Wauben ◽  
H. Kelder

Abstract. With a radiative transfer model, assessments are made of the radiative forcing in northern mid-latitudes due to aircraft emissions up to 1990. Considered are the direct climate effects from the major combustion products carbon dioxide, nitrogen dioxide, water vapor and sulphur dioxide, as well as the indirect effect of ozone production from NOx emissions. Our study indicates a local radiative forcing at the tropopause which should be negative in summer (–0.5 to 0.0 W/m2) and either negative or positive in winter (–0.3 to 0.2 W/m2). To these values the indirect effect of contrails has to be added, which for the North Atlantic Flight Corridor covers the range –0.2 to 0.3 W/m2 in summer and 0.0 to 0.3 W/m2 in winter. Apart from optically dense non-aged contrails during summer, negative forcings are due to solar screening by sulphate aerosols. The major positive contributions come from contrails, stratospheric water vapor in winter and ozone in summer. The direct effect of NO2 is negligible and the contribution of CO2 is relatively small.

2009 ◽  
Vol 9 (19) ◽  
pp. 7397-7417 ◽  
Author(s):  
M. W. Shephard ◽  
S. A. Clough ◽  
V. H. Payne ◽  
W. L. Smith ◽  
S. Kireev ◽  
...  

Abstract. Presented here are comparisons between the Infrared Atmospheric Sounding instrument (IASI) and the "Line-By-Line Radiative Transfer Model" (LBLRTM). Spectral residuals from radiance closure studies during the IASI JAIVEx validation campaign provide insight into a number of spectroscopy issues relevant to remote sounding of temperature, water vapor and trace gases from IASI. In order to perform quality IASI trace gas retrievals, the temperature and water vapor fields must be retrieved as accurately as possible. In general, the residuals in the CO2 ν2 region are of the order of the IASI instrument noise. However, outstanding issues with the CO2 spectral regions remain. There is a large residual ~−1.7 K in the 667 cm−1 Q-branch, and residuals in the CO2 ν2 and N2O/CO2 ν3 spectral regions that sample the troposphere are inconsistent, with the N2O/CO2 ν3 region being too negative (warmer) by ~0.7 K. Residuals on this lower wavenumber side of the CO2 ν3 band will be improved by line parameter updates, while future efforts to reduce the residuals reaching ~−0.5 K on the higher wavenumber side of the CO2 ν3 band will focus on addressing limitations in the modeling of the CO2 line shape (line coupling and duration of collision) effects. Brightness temperature residuals from the radiance closure studies in the ν2 water vapor band have standard deviations of ~0.2–0.3 K with some large peak residuals reaching ±0.5–1.0 K. These are larger than the instrument noise indicating that systematic errors still remain. New H2O line intensities and positions have a significant impact on the retrieved water vapor, particularly in the upper troposphere where the water vapor retrievals are 10% drier when using line intensities compared with HITRAN 2004. In addition to O3, CH4, and CO, of the IASI instrument combined with an accurate forward model allows for the detection of minor species with weak atmospheric signatures in the nadir radiances, such as HNO3 and OCS.


2021 ◽  
Author(s):  
Filippo Calì Quaglia ◽  
Daniela Meloni ◽  
Alcide Giorgio di Sarra ◽  
Tatiana Di Iorio ◽  
Virginia Ciardini ◽  
...  

<p>Extended and intense wildfires occurred in Northern Canada and, unexpectedly, on the Greenlandic West coast during summer 2017. The thick smoke plume emitted into the atmosphere was transported to the high Arctic, producing one of the largest impacts ever observed in the region. Evidence of Canadian and Greenlandic wildfires was recorded at the Thule High Arctic Atmospheric Observatory (THAAO, 76.5°N, 68.8°W, www.thuleatmos-it.it) by a suite of instruments managed by ENEA, INGV, Univ. of Florence, and NCAR. Ground-based observations of the radiation budget have allowed quantification of the surface radiative forcing at THAAO. </p><p>Excess biomass burning chemical tracers such as CO, HCN, H2CO, C2H6, and NH3 were  measured in the air column above Thule starting from August 19 until August 23. The aerosol optical depth (AOD) reached a peak value of about 0.9 on August 21, while an enhancement of wildfire compounds was  detected in PM10. The measured shortwave radiative forcing was -36.7 W/m2 at 78° solar zenith angle (SZA) for AOD=0.626.</p><p>MODTRAN6.0 radiative transfer model (Berk et al., 2014) was used to estimate the aerosol radiative effect and the heating rate profiles at 78° SZA. Measured temperature profiles, integrated water vapour, surface albedo, spectral AOD and aerosol extinction profiles from CALIOP onboard CALIPSO were used as model input. The peak  aerosol heating rate (+0.5 K/day) was  reached within the aerosol layer between 8 and 12 km, while the maximum radiative effect (-45.4 W/m2) is found at 3 km, below the largest aerosol layer.</p><p>The regional impact of the event that occurred on August 21 was investigated using a combination of atmospheric radiative transfer modelling with measurements of AOD and ground surface albedo from MODIS. The aerosol properties used in the radiative transfer model were constrained by in situ measurements from THAAO. Albedo data over the ocean have been obtained from Jin et al. (2004). Backward trajectories produced through HYSPLIT simulations (Stein et al., 2015) were also employed to trace biomass burning plumes.</p><p>The radiative forcing efficiency (RFE) over land and ocean was derived, finding values spanning from -3 W/m2 to -132 W/m2, depending on surface albedo and solar zenith angle. The fire plume covered a vast portion of the Arctic, with large values of the daily shortwave RF (< -50 W/m2) lasting for a few days. This large amount of aerosol is expected to influence cloud properties in the Arctic, producing significant indirect radiative effects.</p>


2013 ◽  
Vol 13 (14) ◽  
pp. 6687-6711 ◽  
Author(s):  
M. J. Alvarado ◽  
V. H. Payne ◽  
E. J. Mlawer ◽  
G. Uymin ◽  
M. W. Shephard ◽  
...  

Abstract. Modern data assimilation algorithms depend on accurate infrared spectroscopy in order to make use of the information related to temperature, water vapor (H2O), and other trace gases provided by satellite observations. Reducing the uncertainties in our knowledge of spectroscopic line parameters and continuum absorption is thus important to improve the application of satellite data to weather forecasting. Here we present the results of a rigorous validation of spectroscopic updates to an advanced radiative transfer model, the Line-By-Line Radiative Transfer Model (LBLRTM), against a global dataset of 120 near-nadir, over-ocean, nighttime spectra from the Infrared Atmospheric Sounding Interferometer (IASI). We compare calculations from the latest version of LBLRTM (v12.1) to those from a previous version (v9.4+) to determine the impact of spectroscopic updates to the model on spectral residuals as well as retrieved temperature and H2O profiles. We show that the spectroscopy in the CO2 ν2 and ν3 bands is significantly improved in LBLRTM v12.1 relative to v9.4+, and that these spectroscopic updates lead to mean changes of ~0.5 K in the retrieved vertical temperature profiles between the surface and 10 hPa, with the sign of the change and the variability among cases depending on altitude. We also find that temperature retrievals using each of these two CO2 bands are remarkably consistent in LBLRTM v12.1, potentially allowing these bands to be used to retrieve atmospheric temperature simultaneously. The updated H2O spectroscopy in LBLRTM v12.1 substantially improves the a posteriori residuals in the P-branch of the H2O ν2 band, while the improvements in the R-branch are more modest. The H2O amounts retrieved with LBLRTM v12.1 are on average 14% lower between 100 and 200 hPa, 42% higher near 562 hPa, and 31% higher near the surface compared to the amounts retrieved with v9.4+ due to a combination of the different retrieved temperature profiles and the updated H2O spectroscopy. We also find that the use of a fixed ratio of HDO to H2O in LBLRTM may be responsible for a significant fraction of the remaining bias in the P-branch relative to the R-branch of the H2O ν2 band. There were no changes to O3 spectroscopy between the two model versions, and so both versions give positive a posteriori residuals of ~ 0.3 K in the R-branch of the O3 ν3 band. While the updates to the H2O self-continuum employed by LBLRTM v12.1 have clearly improved the match with observations near the CO2 ν3 band head, we find that these updates have significantly degraded the match with observations in the fundamental band of CO. Finally, significant systematic a posteriori residuals remain in the ν4 band of CH4, but the magnitude of the positive bias in the retrieved mixing ratios is reduced in LBLRTM v12.1, suggesting that the updated spectroscopy could improve retrievals of CH4 from satellite observations.


2013 ◽  
Vol 13 (1) ◽  
pp. 2415-2456 ◽  
Author(s):  
L. Zhang ◽  
Q. B. Li ◽  
Y. Gu ◽  
K. N. Liou ◽  
B. Meland

Abstract. Atmospheric mineral dust particles exert significant direct radiative forcings and are critical drivers of climate change. Here, we use the GEOS-Chem global three-dimensional chemical transport model (3-D CTM) coupled online with the Fu-Liou-Gu (FLG) radiative transfer model (RTM) to investigate the dust radiative forcing and heating rates based on different dust vertical profiles. The coupled calculations using a realistic dust vertical profile simulated by GEOS-Chem minimize the physical inconsistencies between 3-D CTM aerosol fields and the RTM. The use of GEOS-Chem simulated aerosol optical depth (AOD) vertical profiles as opposed to the FLG prescribed AOD vertical profiles leads to greater and more spatially heterogeneous changes in estimated radiative forcing and heating rate produced by dust. Both changes can be attributed to a different vertical structure between dust and non-dust source regions. Values of the dust AOD are much larger in the middle troposphere, though smaller at the surface when the GEOS-Chem simulated AOD vertical profile is used, which leads to a much stronger heating rate in the middle troposphere. Compared to FLG vertical profile, the use of GEOS-Chem vertical profile reduces the solar radiative forcing effect by about 0.2–0.25 W m−2 and the Infrared (IR) radiative forcing over the African and Asia dust source regions by about 0.1–0.2 W m−2. Differences in the solar radiative forcing at the surface between using the GEOS-Chem vertical profile and the FLG vertical profile are most significant over the Gobi desert with a value of about 1.1 W m−2. The radiative forcing effect of dust particles is more pronounced at the surface over the Sahara and Gobi deserts by using FLG vertical profile, while it is less significant over the downwind area of Eastern Asia.


2011 ◽  
Vol 28 (1) ◽  
pp. 85-93 ◽  
Author(s):  
Ian J. Barton

Abstract Analyses based on atmospheric infrared radiative transfer simulations and collocated ship and satellite data are used to investigate whether knowledge of vertical atmospheric water vapor distributions can improve the accuracy of sea surface temperature (SST) estimates from satellite data. Initially, a simulated set of satellite brightness temperatures generated by a radiative transfer model with a large maritime radiosonde database was obtained. Simple linear SST algorithms are derived from this dataset, and these are then reapplied to the data to give simulated SST estimates and errors. The concept of water vapor weights is introduced in which a weight is a measure of the layer contribution to the difference between the surface temperature and that measured by the satellite. The weight of each atmospheric layer is defined as the layer water vapor amount multiplied by the difference between the SST and the midlayer temperature. Satellite-derived SST errors are then plotted against the difference in the sum of weights above an altitude of 2.5 km and that below. For the simple two-channel (with typical wavelengths of 11 and 12 μm) analysis, a clear correlation between the weights differences and the SST errors is found. A second group of analyses using ship-released radiosondes and satellite data also show a correlation between the SST errors and the weights differences. The analyses suggest that, for an SST derived using a simple two-channel algorithm, the accuracy may be improved if account is taken of the vertical distribution of water vapor above the ocean surface. For SST estimates derived using algorithms that include data from a 3.7-μm channel, there is no such correlation found.


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