DENSITIES AND VIBRATIONAL DISTRIBUTION OF H-3+ IN THE JOVIAN AURORAL IONOSPHERE

被引:63
作者
KIM, YH
FOX, JL
PORTER, HS
机构
[1] SUNY STONY BROOK, DEPT MECH ENGN, STONY BROOK, NY 11794 USA
[2] FURMAN UNIV, DEPT COMP SCI, GREENVILLE, SC 29613 USA
关键词
D O I
10.1029/92JE00454
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Observations of the H-3+ infrared emission at 2 and 4 mum have suggested that H-3+ is in local thermodynamic equilibrium (LTE) in the region of the Jovian ionosphere from which the emissions originate. We have tested this assumption by calculating the vibrational distribution of H-3+ over the altitude range of 350 to 1500 km above the methane cloud tops (1 to 4 X 10(-3) mubar). We have constructed a model of the Jovian auroral ionosphere in which the neutral temperatures are enhanced over those of the mid-latitude ionosphere, as suggested by observations and models of the auroral region. We have modeled the precipitation of 10-keV electrons with an energy flux of 1 erg cm-2 s-1. Both the energy and energy flux are less than those that are implicated in the production of the UV aurora. We have computed the densities and vibrational distribution of H-3+ and find that the distribution of the six lowest states of H-3+ can be determined fairly well in spite of uncertainties in the atomic and molecular data. Since the nearly resonant transfer of vibration from H-2(v=1) is an important process in populating the H-3+ (v1=0,v2=2) state, it is necessary to model the vibrational distribution of H-2 as well. The computed altitude profiles and vibrational distributions of H-3+ and H-2 are consistent with the observations of infrared emission in the 2- and 4-mum regions. The H-3+ is not in LTE near and above the H+ peak, since loss of the H-3+ (v1=0,v2=1) and H+ (v1=0,v2=2) states by radiation is approximately equal to the collisional loss rate.
引用
收藏
页码:6093 / 6101
页数:9
相关论文
共 65 条
[1]   MEASUREMENTS OF DISSOCIATIVE RECOMBINATION COEFFICIENTS OF H-3+, HCO+, N2H+, AND CH5+ AT 95-K AND 300-K USING THE FALP APPARATUS [J].
ADAMS, NG ;
SMITH, D ;
ALGE, E .
JOURNAL OF CHEMICAL PHYSICS, 1984, 81 (04) :1778-1784
[2]  
ADAMS NG, 1987, IAU S, V120, P1
[3]   SIMPLE ULTRAVIOLET CALIBRATION SOURCE WITH REFERENCE SPECTRA AND ITS USE WITH THE GALILEO ORBITER ULTRAVIOLET SPECTROMETER [J].
AJELLO, JM ;
SHEMANSKY, DE ;
FRANKLIN, B ;
WATKINS, J ;
SRIVASTAVA, S ;
JAMES, GK ;
SIMMS, WT ;
HORD, CW ;
PRYOR, W ;
MCCLINTOCK, W ;
ARGABRIGHT, V ;
HALL, D .
APPLIED OPTICS, 1988, 27 (05) :890-914
[5]  
Allison A. C., 1970, Atomic Data, V1, P289
[7]   THE DISSOCIATIVE RECOMBINATION RATE COEFFICIENTS OF H-3+, HN2+, AND HCO+ [J].
AMANO, T .
JOURNAL OF CHEMICAL PHYSICS, 1990, 92 (11) :6492-6501
[8]   A COMPUTER STUDY OF THE FORMATION OF H-3+ AND ITS VIBRATIONAL DEACTIVATION USING A STATISTICAL-MODEL [J].
ANICICH, VG ;
FUTRELL, JH .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY AND ION PROCESSES, 1984, 55 (02) :189-215
[9]   JUPITER - STRUCTURE AND COMPOSITION OF THE UPPER-ATMOSPHERE [J].
ATREYA, SK ;
DONAHUE, TM ;
FESTOU, MC .
ASTROPHYSICAL JOURNAL, 1981, 247 (01) :L43-L47
[10]  
ATREYA SK, 1986, ATMOSPHERES IONOSPHE, P124