Showing papers by "Julianne I. Moses published in 2011"

DISEQUILIBRIUM CARBON, OXYGEN, AND NITROGEN CHEMISTRY IN THE ATMOSPHERES OF HD 189733b AND HD 209458b

Abstract: We have developed a one-dimensional photochemical and thermochemical kinetics and diffusion model to study the effects of disequilibrium chemistry on the atmospheric composition of “hot-Jupiter” exoplanets. Here we investigate the coupled chemistry of neutral carbon, hydrogen, oxygen, and nitrogen species on HD 189733b and HD 209458b and we compare the model results with existing transit and eclipse observations. We find that the vertical profiles of molecular constituents are significantly affected by transport-induced quenching and photochemistry, particularly on the cooler HD 189733b; however, the warmer stratospheric temperatures on HD 209458b help maintain thermochemical equilibrium and reduce the effects of disequilibrium chemistry. For both planets, the methane and ammonia mole fractions are found to be enhanced over their equilibrium values at pressures of a few bar to less than an mbar due to transport-induced quenching, but CH4 and NH3 are photochemically removed at higher altitudes. Disequilibrium chemistry also enhances atomic species, unsaturated hydrocarbons (particularly C2H2), some nitriles (particularly HCN), and radicals like OH, CH3, and NH2. In contrast, CO, H2O, N2, and CO2 more closely follow their equilibrium profiles, except at pressures 1 μbar, where CO, H2O, and N2 are photochemically destroyed and CO2 is produced before its eventual high-altitude destruction. The enhanced abundances of CH4, NH3, and HCN are expected to affect the spectral signatures and thermal profiles of HD 189733b and other relatively cool, transiting exoplanets. We examine the sensitivity of our results to the assumed temperature structure and eddy diffusion coefficients and discuss further observational consequences of these models.

Disequilibrium Carbon, Oxygen, and Nitrogen Chemistry in the Atmospheres of HD 189733b and HD 209458b

Abstract: We have developed 1-D photochemical and thermochemical kinetics and diffusion models for the transiting exoplanets HD 189733b and HD 209458b to study the effects of disequilibrium chemistry on the atmospheric composition of "hot Jupiters." Here we investigate the coupled chemistry of neutral carbon, hydrogen, oxygen, and nitrogen species, and we compare the model results with existing transit and eclipse observations. We find that the vertical profiles of molecular constituents are significantly affected by transport-induced quenching and photochemistry, particularly on cooler HD 189733b; however, the warmer stratospheric temperatures on HD 209458b can help maintain thermochemical equilibrium and reduce the effects of disequilibrium chemistry. For both planets, the methane and ammonia mole fractions are found to be enhanced over their equilibrium values at pressures of a few bar to less than a mbar due to transport-induced quenching, but CH4 and NH3 are photochemically removed at higher altitudes. Atomic species, unsaturated hydrocarbons (particularly C2H2), some nitriles (particularly HCN), and radicals like OH, CH3, and NH2 are enhanced overequilibrium predictions because of quenching and photochemistry. In contrast, CO, H2O, N2, and CO2 more closely follow their equilibrium profiles, except at pressures < 1 microbar, where CO, H2O, and N2 are photochemically destroyed and CO2 is produced before its eventual high-altitude destruction. The enhanced abundances of HCN, CH4, and NH3 in particular are expected to affect the spectral signatures and thermal profiles HD 189733b and other, relatively cool, close-in transiting exoplanets. We examine the sensitivity of our results to the assumed temperature structure and eddy diffusion coefficientss and discuss further observational consequences of these models.

Quenching of Carbon Monoxide and Methane in the Atmospheres of Cool Brown Dwarfs and Hot Jupiters

Abstract: We explore quench kinetics in the atmospheres of substellar objects using updated timescale arguments, as suggested by a thermochemical kinetics and diffusion model that transitions from the thermochemical-equilibrium regime in the deep atmosphere to a quench-chemical regime at higher altitudes. More specifically, we examine CO quench chemistry on the T dwarf Gliese 229B and CH4 quench chemistry on the hot-Jupiter HD 189733b. We describe a method for correctly calculating reverse rate coefficients for chemical reactions, discuss the predominant pathways for interconversion as indicated by the model, and demonstrate that a simple timescale approach can be used to accurately describe the behavior of quenched species when updated reaction kinetics and mixing-length-scale assumptions are used. Proper treatment of quench kinetics has important implications for estimates of molecular abundances and/or vertical mixing rates in the atmospheres of substellar objects. Our model results indicate significantly higher Kzz values than previously estimated near the CO quench level on Gliese 229B, whereas current-model-data comparisons using CH4 permit a wide range of Kzz values on HD 189733b. We also use updated reaction kinetics to revise previous estimates of the Jovian water abundance, based upon the observed abundance and chemical behavior of carbon monoxide. The CO chemical/observational constraint, along with Galileo entry probe data, suggests a water abundance of approximately 0.51-2.6 × solar (for a solar value of H2O/H2 = 9.61 × 10–4) in Jupiter's troposphere, assuming vertical mixing from the deep atmosphere is the only source of tropospheric CO.

Quenching of Carbon Monoxide and Methane in the Atmospheres of Cool Brown Dwarfs and Hot Jupiters

Abstract: We explore CO-CH4 quench kinetics in the atmospheres of substellar objects using updated time-scale arguments, as suggested by a thermochemical kinetics and diffusion model that transitions from the thermochemical-equilibrium regime in the deep atmosphere to a quench-chemical regime at higher altitudes. More specifically, we examine CO quench chemistry on the T dwarf Gliese 229B and CH4 quench chemistry on the hot-Jupiter HD 189733b. We describe a method for correctly calculating reverse rate coefficients for chemical reactions, discuss the predominant pathways for CO-CH4 interconversion as indicated by the model, and demonstrate that a simple time-scale approach can be used to accurately describe the behavior of quenched species when updated reaction kinetics and mixing-length-scale assumptions are used. Proper treatment of quench kinetics has important implications for estimates of molecular abundances and/or vertical mixing rates in the atmospheres of substellar objects. Our model results indicate significantly higher Kzz values than previously estimated near the CO quench level on Gliese 229B, whereas current model-data comparisons using CH4 permit a wide range of Kzz values on HD 189733b. We also use updated reaction kinetics to revise previous estimates of the Jovian water abundance, based upon the observed abundance and chemical behavior of carbon monoxide. The CO chemical/observational constraint, along with Galileo entry probe data, suggests a water abundance of approximately 0.51-2.6x solar (for a solar value of H2O/H2=9.61E-04) in Jupiter's troposphere, assuming vertical mixing from the deep atmosphere is the only source of tropospheric CO.

Hydrocarbon ions in the Lower Ionosphere of Saturn

Abstract: [1] Radio occultation measurements of the Saturn ionosphere have shown that persistent but variable electron density layers appear well below the major peaks. We model here the region of hydrocarbon ions that is below the main peak and is produced by absorption of solar photons in the wavelength range 842 to 1116 A, which penetrate to altitudes below the methane homopause in the wings of the H2 absorption lines, and in the gaps between groups of lines. In this wavelength range, H2 absorbs photons in discrete transitions to rovibrational levels of electronically excited states, which then decay to a range of rovibrational levels of the electronic ground state, or to the continuum of the ground state. The cross sections for these discrete absorptions vary by several orders of magnitude from the peaks to the wings of the absorption lines. We find that the adoption of high resolution photoabsorption cross sections for the H2 bands leads to different photoionization profiles for both the hydrocarbons and H atoms, and to peak inline imagephotoproduction profiles that are more than an order of magnitude larger than those computed with low resolution cross sections. For the present model, we find that ionization by energetic electrons that accompany the absorption of soft X-rays appears in the same altitude range. We predict that a broad region of hydrocarbon ions appears well below the main peak, in the altitude range 600 to 1000 km above the 1 bar level (2–0.04 μbar) with a maximum electron density of ∼3×103cm−3 at low solar activity.