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Detailed Reference Information |
Hallett, J.T., Shemansky, D.E. and Liu, X. (2005). Fine-structure physical chemistry modeling of Uranus H2 X quadrupole emission. Geophysical Research Letters 32: doi: 10.1029/2004GL021327. issn: 0094-8276. |
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A new hydrogen physical chemistry model has been developed at the fine-structure level for application to the giant outer planet thermospheres. The model is applied to Uranus because observations of dayglow H2 X 1Σg+ (v) quadrupole and H3+ vibration-rotation emission made at NASA IRTF and UKIRT provide critical constraints for thermospheric modeling. The observed H3+ vibration-rotation emission infers an H3+ dominant ionosphere, predicted only for non-LTE H2 X (v : J). Excitation mechanisms explored are solar and non-solar electron energy deposition. Non-solar electron forcing is constrained by the EUV H2 Lyman and Werner band emission measured by Voyager UVS. Analysis indicates that non-solar electrons are dominant in the energy budget required to predict the observed thermospheric temperature profile. The modeled H2 X quadrupole emission infers that an additional mechanism is required to excite the H2 X (v = 1) population. Non-thermal H produced in dissociative excitation of H2 X is a primary candidate. |
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BACKGROUND DATA FILES |
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Abstract |
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Keywords
Atmospheric Composition and Structure, Ion chemistry of the atmosphere (2419, 2427), Atmospheric Composition and Structure, Thermosphere, energy deposition, Planetary Sciences, Fluid Planets, Atmospheres (0343, 1060), Planetary Sciences, Fluid Planets, Ionospheres, Planetary Sciences, Solar System Objects, Uranus |
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Publisher
American Geophysical Union 2000 Florida Avenue N.W. Washington, D.C. 20009-1277 USA 1-202-462-6900 1-202-328-0566 service@agu.org |
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