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Nightside Ionosphere of Mars: Composition, Vertical Structure, and Variability

Authors :
Girazian, Z
Mahaffy, P. R
Lillis, R. J
Benna, Mehdi
Elrod, Meredith K
Jakosky, B. M
Source :
Journal of Geophysical Research: Space Physics. 122(4)
Publication Year :
2017
Publisher :
United States: NASA Center for Aerospace Information (CASI), 2017.

Abstract

We provide an overview of the composition, vertical structure, and variability of the nightside ionosphere of Mars as observed by Mars Atmosphere and Volatile EvolutioN (MAVEN)'s Neutral Gas and Ion Mass Spectrometer (NGIMS) through 19 months of the MAVEN mission. We show that O+2 is the most abundant ion down to ∼130 km at all nightside solar zenith angles (SZA). However, below 130 km NO+ is the most abundant ion, and NO+ densities increase with decreasing altitude down to at least 120 km. We also show how the densities of the major ions decrease with SZA across the terminator. At lower altitudes the O+2 and CO+2 densities decrease more rapidly with SZA than the NO+ and HCO+ densities, which changes the composition of the ionosphere from being primarily O+2 on the dayside to being a mixture of O+2, NO+, and HCO+ on the nightside. These variations are in accord with the expected ion-neutral chemistry, because both NO+ and HCO+ have long chemical lifetimes. Additionally, we present median ion density profiles from three different nightside SZA ranges, including deep on the nightside at SZAs greater than 150∘ and discuss how they compare to particle precipitation models. Finally, we show that nightside ion densities can vary by nearly an order of magnitude over month long timescales. The largest nightside densities were observed at high northern latitudes during winter and coincided with a major solar energetic particle event.

Details

Language :
English
Volume :
122
Issue :
4
Database :
NASA Technical Reports
Journal :
Journal of Geophysical Research: Space Physics
Notes :
NNH15CO48B, , 80GSFC17M0002, , NNG17PT01A
Publication Type :
Report
Accession number :
edsnas.20180003592
Document Type :
Report
Full Text :
https://doi.org/10.1002/2016JA023508