Wright State University CORE Scholar Physics Faculty Publications 1990 A Signature of Auroral Precipitation in the Nightside Ionosphere of Venus Jane L. Fox H. A. Taylor Jr. Follow this and additional works at: http://corescholar.libraries.wright.edu/physics Part of the Physics Commons Repository Citation Fox, J. L., & Taylor, H. A. (1990). A Signature of Auroral Precipitation in the Nightside Ionosphere of Venus. Geophysical Research Letters, 17 (10), 1625-1628. http://corescholar.libraries.wright.edu/physics/327 This Article is brought to you for free and open access by the Physics at CORE Scholar. It has been accepted for inclusion in Physics Faculty Publications by an authorized administrator of CORE Scholar. For more information, please contact [email protected]. Physics GEOPHYSICAL RESEARCH LETTERS, VOL. 17,NO. 10,PAGES1625-1628, SEPTEMBER 1990 A SIGNATUREOF AUROtLiLPRECIPITATIONIN THE NIGHTSIDEIONOSPHEREOF VENUS J. L. Fox InstituteforTerrestrial andPlanetary Atmospheres StateUniversity ofNewYorkat StonyBrook H. A. Taylor, Jr. TaylorEnterprises, BeaverRiver,NovaScotia Abstract. We show here that the densities of mass- plainedsinceN2 + reactsrapidlywithO to produce NO+ 28 ionsmeasuredby the Pioneer Venus Orbiter ion mass Nt + O -+ NO+ + N. spectrometer (OIMS) onthenightside ofYenusarehighly ,ariab!e and show little correlation with the values of the Becauseof the high ionizationpotentialsof both N2 and CO, the chemicalsourcesare limited. Yet a survey of early Pioneer Venus orbits with periapsisbelow 165 km reveals a large variability in the maximum densitiesof 0 + densities.We have determinedthe total production ratesof mass-28ionsin the chemicalequih'briumregion and •nd that this production rate cannot be explained by known chemicalproduction reactions. We propose that the "excess"production is due to precipitation of electronsinto the nightsidethermosphere. mass-28 ionswithvalues rangingfromabout10 cm-3 to about104cm -3. Tayloret al. [1982]hadearlierremarked thattheoccasional largedensities of NO+ andO• mea- The sourceof the Venus nightsideionospherehas been disputedsincethe first radio occultationmeasurementsof sured by the OIMS appeared to require a sourcein addition to ion transpo•; they suggestedthat the densities were enhancedby particle precipitation, but the mechanism of the sourcewas not resolved. We propose that thenightside electrondensityprofileby Mariner5 [K!iore the excess NO+ is produced fromN2 + created by parti- etal.,1967].Sincethen,theviablemechanisms,have been cle precipitation,and that high densitiesof mass-28ions in the nightsideionosphereare an in situ signature of precipitation of electronsinto the nightsideatmosphere. Introduction reducedto two: transport of atomic ions, mostly O+, from the daysideand precipitation of energetic electrons that havebeen observedin the Venusumbra. Models appropriate to high solar activity have shown that plasma transport is the dominant maintenance mechan•m, since In the discussionthat follows, we identify the sources and sinksof mass-28ions.in the chemicaleq 'ui!ibriumregion, that below approximately165-170kin. There the ion productionand lossrates are equal, so the magnitude it alonecanproducethe observeddensitiesof O+, with electronprecipitation playing a possiblesecondaryrole of the source can be estimated because the total loss rate in enhancing the lower02+ peak[Spenner et al., 1981; can be computed fairly accurately. From the loss rate and the known chemical sources, the %xcess" production rate, that we ascribehere to particle precipitation, Cravenset al., 1983]. Gringauzet al. [1977']maintain that precipitation of electronsalone is sufficient to pro- is determined. ducethe main ion peak, as measuredby the Venera9 and !0 radio occultationexperimentsat solar minimum. We havebeeninvestigatingthe chemistryof the nightsideionosphere,with a view towazd elucidatingthe relative roles of electron precipitation and plasma trans- Sources ofN•+ andCO+ Reactions,referencesand rate coefficientsused in this work are summarized in Table 1, and the reactions num- port in its maintenance. Model calculations based on bers cited below refer to the numbers in that table. Be- ion transport as the sourceof the nightside ionosphere causeof the highionizationpotentia!of N2 (15.58eV), only a few chargetransferreactionsof atmosphericspe- sho•ed that the reaction ot + N -+ ciesareenergetically capable ofproducing N•+, including charge transfer fromHe+, 0 ++ andO+(2D)(reactions 3- ++ o 5). Reaction(3) • potentiallyimportant,sincenighttime He+ densitiesare largerthan daytimevalues,peakingin the the pre-dawnsector[Tayloret al., 1980]. Densities of O++ weremeasuredby the PV OIMS, but are often wasthe major sourceof NO+in the chemicalequilibrium region.Ana!y-sis of data from eight P•neer Venus(PV) orbitschosen lot lowperiapshand the availabilityof data showedthat the NO + densities could be modeled with re- above the noise level of the instrtunent only above the action(1) asthe solesourceforsomeorbits,but forothers it wascompletely inadequate.A closelookat thoseorbits showed that they werean character• by high densities chemicalequilibriumregion.In addition,the product•of reaction(4) are unknown;the large exothermidtysuggeststhat the dissociativechanne!probablydominates. ofmass-28 ions(N•+ + CO+)..Thisdeviation is easilyex- Charge transfer from0+(2/)) to N2,reaction (5), isa major source of N2 + in thedayside ionosphere [Fax,1•2], and the importanceof t]:dsreaction dependson whet.her Copyright 1990 by the American Geophysical Union. the roetastable O+(2D) ioncouldsurvivetransportfrom the dayside. A detailed analysiswo•d be required to Paper number 90GL01458 0094-8276 / 90 / 9 0GL-0! 4 5:8503.00 modelthe roleof reaction(5) in producing the observed !625 ! 626 Fox and Taylor: Auroral Signaturein VenusIonosphere Table1. Ratecoefficients forreactions involved in thechemistry ofN•+ andCO+ in theVenus nightside ionosphere. No. Reaction Rate Coefficient (cm3s -•) References (2) N•+ + O --,NO+ + N 1.4(-10)a(300/Ti) 0'44 McFarland et al. (197'4) _• 1.6(-9)b Anicichet al. (1977) Howorkaet al. (1979) Johnsenand Biondi(1980) (3) (4) He+ + Ns--*N2 + + He O++ + Ns-• N•+ + 0 + O+(2D)+N• • N•+ + O (6) He+ + COs • He + CO+ + 0 O++ + COs -• CO+ + O+ + O O ++ + CO -• CO + + O + (9) C+ + CO•. -+ CO+ + CO N + + COs -* CO + + NO (11) N + + CO -+ CO + + N CO + + O -, CO + 0 + 5.9(--10) (13) (14) ++ + CO* CO+ + CO• -• CO• + + CO N•++e•N+N ?.?(--10) 1(-9) (16) CO +.+ e-* C+ 0 a. Read 1.4 x 10- xø AdamsandSmith(1976);Rakshitet al. (1978) _<2(-9) _• 1.6(-9)b (8) - Johnsen and Biondi c (assumed the sameasfor reaction5) z)(3oo/i. 2(- ?)(300/T,)ø'4s Fahey et al. (1981) Smith et al. (197'8) Miller et al. (1984) Fehsenfeld and Ferguson(197'2) Smith et al. (1978) Adamset al. (1978) (98o) MitchellandHus (1985) b. The productsin the reactionsof 0 ++ are unknown,sothe rate coefficients are upperlimits only. c. Private communication to Fox and Victor (1981). N•+, butwewillshowbelowthatit canberuledouton imate the total lossrate of mass-28ionswe usedaveraged morphologicalgrounds. CO also has a fairly high ionization potential of 14.01 values for the rate coefficients. Errors of less than 15% eV. CO+ can be producedby the dissociativecharge transferreactionof He+ with CO•. (reaction6) with a yield of about 79%. The reactionof He+ with CO producesverylittle CO+ , resultingalmostcompletelyin dissociativeionization[Rakshitet al., 1978]. Productionof CO+ in thereactionof O++ with CO2 and with CO (reactions7 and 8) is energeticallyfeasible,but the products in these reactions are unknown. Other possible production mechanismsare reactionsof C+ and N + with COs and CO (reactions9-11). Thesereactionsare potentially important,sinceC+ andN+ shouldbe transportedfrom the daysidealongwith O+, althoughwith muchsmaller or so, substantially lessthan the uncertainty in the rate coefficientsthemselves,result from this assumption. 220 200 180 J• The source due to chemical reactions can be computedif the densitiesof the speciesinvolved are measured. The OIMS measureddensitiesof He+, O++, C+, and N +, but valuesare not availablefor all of the nightsidepassesof the PVO, nor at all altitudes. Nonetheless,it is possibleto computethe sourceof mass28 ionsdueto reactions(3-11) for a numberof orbitsover somepart of the chemicalequilibrium region. Total Production Rate of Mass-28 Ions ;,"'..,,-'?-' : _+ ,' ..• •__-'.,.'-'.•--. ...... :: ....... •,•..... •-.-•,. 140 1 160 2 3 4 5 LOGIONDENSITIES (CM-•) b. -- '"'ol'':' I'' "'I''' '..... '.... cially electronimpact, on Ns, CO and COs remains a viable mechanism. '; _.•. '•, 2•' .-,.NO..-' F 160 fluxes. If chemical sourcesare insufficient to produce the observed mass-28ion densities, only particle impact, espe- L 150 o 140 ,,, 0 l,.... , ,, )',, , , ) , ,,, 1 2 3 4 LOGPRODUCTION ORLOSSRATE(CM-aS -•) Fig. la. Densities of majorionsfor orbit505 (inbound) from PV orbiter ion massspectrometerdata. lb. Total productionrate of mass-28ions(filledcircles),production rate due to chemicalreactions(opencircles)and excess production (opensquares), for Orbit 505(inbound). SincebothN•+ andCO+ contribute to the measured Figuresla and 2a showthe major ion densitiesfor or- density,it is not possibleto computethe total lossrate exactly. Fortunately,however,the rate coefcients for bits 505 and 529. Periapsesfor orbits 505 and 529 were the majorreactions of CO+ andN2 + arenearlyequal, at 22.1 and0.7 hourslocaltime andsolarzenith anglesof so an approximatevaluefor the total lossrate can be !49.5 ø and 163.2ø, respectively,so both orbits were near obtained. The most important lossmechanismfor both the antisolarpoint. The maximum mass-28ion density is a factorof morethan 25 largerfor orbit 529 than orbit ionsis reactionwith 0 (reactions2 and 12). The rate coefficients for both reactions(2) and (12) are closeto 1.4x 10-•øcm3s -z. N•+ andCO+ alsoreactat nearlygas kineticrateswith C02 (reactions 13 and 14). Dissociariverecombination (reactions 15and16)isthemajorloss mechanism for both ionsat high altitudes. Rate coefcientsof 2.2 x 10-z and 2.0 x 10-7 cm3s-x at 300 K have beenreported forN•+ andCO+, respectively. Toapprox- 505. Figureslb and 2b comparethe total lossratesof mass-28ions(reactions2 and 12-16) to the production ratesdueto reactions(3-11) in the chemicalequilibrium regionfor the two orbits. The maximummass-28ion lossrate for orbit 529 is about 104cm-3s-•, whereasthe productionrate dueto chemical reactionsis only 10- 20 cm-as -•. Theexcess production is onthe orderof 104 FoxandTaylor:AuroralSignature in Venus Ionosphere 220 titude below 1(35kin, and data at the mass-28 ion peak , for thedensities of O+, O•+, He+, CO•, O, andN•. In - - this calcui•tion,only the reactionsof He+ (reactions3 200 - and •) wereincludedaschemicalsourcesof mass-28ions, - - since experiencewith individual orbits showed the other sourcesto be unimportant. The electron temperature was assumedto be about I000 K for all the data points. 180 - . - 1•0 _ -- 140 -, 1 • , • I • • • , I ,,,,• ,,,,, I • • f ,- 2 3 4 LOGION DENSITIES (CM-•) 160 ß Errors resultingfrom this assumptionshould be small, since the electron temperature dependenceof the dissociative recombination coefficientis weak, and dissociative recombinationis not the major lossmechanism. In order to reduce the effectsof variability due to changesin the neutral atmosphereand in the altitude of periapsis, the excessproduction"frequency"was obtainedby dividing 150 the rate by the factor$[N•.]4-0.1[CO•]. The first term ø% 140 o 1627 1 2 in the factor representsionization of N• and CO, and was chosenbecausethe CO density is about twice the N• • Fig. 2. Sameas for Fig. 1, but for Orbit 529 (inbound). In Fig. 2b, the total productionrate and excessproduction rate axe essentially superimposed. cm-as-x. For orbit 505, the maximumauroralproduction rate is about a factor of 40 less than for orbit 529, althoughthe production rates due to chemicalreactions are about the same for the two orbitsß Other evidence for the precipitation of electrons into the nightsidethermosphereexists. Fluxes of su,pratherreal electronshave been measuredabovethe atmosphere in the Venusumbraby the PV retardingpotentialanalyzer(ORPA) [e.g. Knudsen"andMiller, •985] as well as by the plasma analyzers on the Soviet Venera 9 and 10 spacecraft[e.g. Gringauzet al., 1977]. Continuous but highly variable emissionsof atomic oxygen at 1304 and1356]k.havebeenobserved in images of the nightsideof Venusby the P V orbiter ultraviolet spectrometer densityon the nightsideabovethe homopause tHedinet al., 1983]. The secondterm representsthe contribution of dissociativeionization of CO•; the factor 0.10 is the high energy ratio of the electron impact crosssections for productionof CO+ from CO• and CO. On the dayside, the excessproduction is due to direct ionization and chemicalreactionotherthan reactions(3) and (6). The production frequencyappearslarge on the dayside also becauseCO is moreabundantrelativeto N•. there tHedin et al., 1983].The variabilityon the daysideis small,because all the data were taken near solar maximum, but somescatter remainsfrom the variation of periapsisalti- tude. The largevariabilityin the sourceon the nightside, ranging over more than two orders of magnitude, itself suggestsparticle precipitation as the sourcemechanism. Some excessproductionappears to be present in nearly all the orbits. This is consistentwith the morphologyof the1304• aurora[Phillips et al., !986],whichis nearly alwaysvisibleon the nightside,but exhibitslarge spatial and temporal variations. (OUVS) [phillipset al., 1986]. Fox and Stewart[1990] haveproposedthat theseemissionsaxecausedby the precipitationof soft electronsinto the nightsideatmosphere. ø -4 ' ß ' d,'• "..,..• I ;- J-' ;," ß ' ,,,ira, .h•/" .. . '•-' '• ; -- :":... ! , _ . o '1' 0 14 8 !2 it) 20 24 LOCAL TIME o o Fig. 4. Ratioof [28+][0]/[N•]at the mass-28 ionpeakto the densityof O+ •t its peak,as a functionof local•ime for the first 600 orbits. The variability on the nightsideis substantiallygreaterthan •he •riability on the dayside. Fig. 3. Productionfrequency of mass-28ionsin excess of that that can be accountedfor by chemicalreactions at the mass-28ion peak as a functionof local time for -all orbits of the first 600 for which sut•ci.ent data are available. Figure 3 showsthe exce• .t)roduction" --u•'ncy -•' of mass-28ionsat the mass-28ion peak for all orbits among •hefirst600that meetthefollowing criteria:periapsis Since models have shown that the measured 0 + densi- ties can only be accountedfor by transport from the dayside, and if mass-28ionsare mostly producedby auroral processes,the relative values of the maximum m•28 ion and 0 + densities would be indicative of the relative importance of ion transport and particle precipitation in the nightsideionosphere. Figure4 is a plot of the ratio of thepeakmass-28 iondensity(dividedby [N•]/[O]) to the peak0 + densityasa functionof localtime for all orbits 1628 Fox and Taylor: Auroral Signaturein VenusIonosphere with periapsi$below 165 km and with availablemass-28 Fox, J. L. and G. A. Victor, O++ in the Venusianiono- ion, 0 +, N2 and Oder.sities.Here the factor [N2]/[O] is sphere,J. Geophys.Res., 86, 2438, 1981. Gringauz, K. I., M. I. Verigin, T. K. Breus and T. Gom- chosento limit the scatter due to the variability of the neutral atmosphereand the changein the altitude of peflapsis. The remaininglarge orbit to orbit variability is itself ir.dicative of particle precipitation as the source of the mass-28ion. The occurrenceof very high values is of particular interest, as it showsthat sufficientelectron precipitation is present, at least occasionally,to affect the ion densitiessubstantially. The large variation in the ratio also showsthat high mass-28 ion densities are not correlatedwith high O+ densitiesand that transport of 0 + (2D) is unlikelyasa sourceof mass-28 ions,sincethe transport of the metastable ion would be expected to be correlatedwith the transportof O+. Conclusions We have shown that the total production rate of mass28 ions in the Venus nightside ionosphere cannot be accountedfor by chemicalproduction resulting from transport of atomic ions from the dayside for a substantial number of orbits of the Pioneer Venus spacecraft. We ascribethe missingproduction to precipitation of particles, possibly the same electrons that are implicated in the production of the ultraviolet "auroral" emissions. A study of the production rate at the mass-28 ion density maximum for all orbits of the first 600 for which sufficient data are available shows that the auroral production rate is highlyvariable,with maximumvaluesof about 10't cm-Ss-•. Thisgreatvariabilitypointsto particleprecipitation as the source. Acknowledgments.JLF thanks NASA Goddard Space Flight Center for their hospitality and aid in accessing the UADS data base. This work has been supported in part by NASA grants NAGW-665 and NAG2-523 to the State University of New York. References Adams, N. G. and D. Smith, Product ion distributions for someion-moleculereactions, Y. Phys. B., 9, 1439, 1976. Adams, N. G., D. Smith and D. Grief, Reactions of HnCO+ with moleculesat 300 K, Int. Y. Mass $pectr. Ion Phys., œ6,405, 1978. Anicich,V. G., J. B. Laudenslager,W. T. Huntress,and J. H. Futrell, J. Chem. Phys 67, 4340, 1977. Craver.s, T. E., S. L. Crawford, A. F. Nagy and T. I. Gombosi,A two-dimensional modelof the ior,osphere of Venus, Y. Geophys.Res. 88, 5595, 1983. Fahey,D. W., F. C. Fehsenfeld,and E. E. Ferguson,Rate constam for the reaction C+ + C02 at collision en- bosi, Electroncurrentsmeasuredin the opticalshadow of Venus by the Venera-9 and Venera-10 satellites, Soy. Phys. Dokl., 22, 53, 1977. Hedin, A. E., H. B. Niemann, W. T. Kasprzak, and A. Seiff, Global empirical model of the Venus thermosphere, J. Geophys. Res., 88, 73, 1983. Howorka, F., et al., Laboratory studies of O++ reac- tionsof ionospheric importance,J. Geophys.Res., 8•{, 5941, 1979. Kliore, A., et al., Atmosphere and ionosphere of Venus from the Mariner V S-band radio occultation mea- surement, Science, 158, 1683, 1967. Knudsen, W. C. and K. L. Miller, Pioneer Venus superthermal electron flux measurementsin the Venus umbra, J. Geophys.Res., 90, 2695, 1985. 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Spermer, K., et al., On the maintenance of the Vetres nightside ionosphere: electron precipitation and plasma transport, J. Geophys.Res., 86, 9170, 1981. Taylor, H. A., Jr., et al., Global observationsof the composition and dynamics of the ionosphereof Venus: Implicationsfor solarwind interaction,Y. Geophys. Res., 85, 7765, 1980. Taylor, H. A., Jr., et al., Observedcompositionof the ionosphereof Venus: implications for the ionization peak ar.d the maintenanceof the nightsideionosphere, Icarus, 51, 283, 1982. Zipf,E. C., The dissociative recombination ofvibrational- ly excitedN•+ ions,Geophys.Res. Left., 7, 645, 1980. ergies0.04 to 2.5 eV, Geophys.Res. Left, 8, 1115, 1981. Fehsenfeld,F. C., and E. E. Ferguson,Thermal energy reaction rate constantsfor H + and CO + with O and NO, or. Chem. Phys, 56, 3066, 1972. Fox, J. L., The chemistryof roetastablespeciesin the J. L. Fox, Departmentof MechanicalEngineering,State University of New York, Stony Brook, NY 11794. H. A. Taylor, Jr., TaylorEnterprises,R. R. 1, Box2495, Beaver River, Nova Scotia B5A 4A5, Canada. Venustanionosphere,Icarus, 5i, 248, 1982. Fox,J. L. and A. I. F. Stewart,The Venusultravioletaurora: a soft electronsource,submitted to J. Geophys. Res., 1990. (ReceivedJune 4, 1990; acceptedJune 19, 1990.)
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