Lecture 5: Hydrogen Escape, Part 1

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41st Saas-Fee Course From Planets to Life 3-9 April 2011 Lecture 5: Hydrogen Escape, Part 1 Prebiotic O 2 levels/ Kinetic theory of gases/ Jeans escape/ Nonthermal escape J. F. Kasting

Why do we care about hydrogen escape? Most H comes initially from H 2 O. Thus, when H escapes, O is left behind terrestrial planets become more oxidized with time, even without biology Atmospheric scientists got the prebiotic O 2 level wrong for many years before Jim (J.C.G.) Walker finally got it right The reason they got it wrong was because they didn t understand hydrogen escape This problem is important, because it bears on the question of whether O 2 in an exoplanet atmosphere is a sign of life

Prebiotic O 2 levels historical Berkner and Marshall (1964, 1965, 1966, 1967) tried to estimate prebiotic O 2 concentrations They recognized that the net source of O 2 was photolysis of H 2 O followed by escape of H to space These authors assumed that O 2 would build up until it shielded H 2 O from photolysis perspective

UV absorption coefficients of various gases S-R continuum Schumann -Runge bands Herzberg continuum Source: J.F. Kasting, Ph.D. thesis, Univ. of Michigan, 1979

Berkner and Marshall s model Resulting O 2 mixing ratio is of the order of 10-3 to 10-4 PAL (times the Present Atmospheric Level) Don t worry if you can t read this graph, because their conclusion is completely wrong!

Brinkman s model Brinkman (Planet. Space Sci. 19, 791-794, 1971) predicted abiotic O 2 concentrations as high as 0.27 PAL Sinks for O 2 He included a sink due to crustal oxidation, but he neglected volcanic outgassing of reduced species (e.g., H 2, CO) Source of O 2 He assumed that precisely 1/10 th of the H atoms produced by H 2 O photolysis escaped to space. This fraction is much too high Not until 1973 did we understand what controls the hydrogen escape rate on Earth. Don Hunten (J. Atmos. Sci., 1973) figured this out while studying H escape from Saturn s moon, Titan

Hydrogen escape Hydrogen escape can be limited either at the exobase (~500 km altitude) or at the homopause (~100 km altitude) Exobase the altitude at which the atmosphere becomes collisionless An exobase may not exist in a hydrogen-dominated upper atmosphere get hydrodynamic escape In any case, the factor limiting H escape in this case is energy (from solar EUV heating) Mean free path = local scale height = molecular collision cross section

Hydrogen escape (cont.) Homopause the altitude at which molecular diffusion replaces eddy diffusion as the dominant vertical transport mechanism Light gases separate out from heavier ones above this altitude The flux of hydrogen through the homopause is limited by diffusion Homopause 100 km Exobase 500 km

Hydrogen escape (cont.) Molecular diffusion Eddy diffusion (log scale)

500 Exosphere (Collisionless) Exobase H Altitude (km) 100 Heterosphere (Molecular diffusion light gases separate from heavier ones) Homopause H or H 2 0 Homosphere (Eddy diffusion gases are well-mixed) Surface

Hydrogen escape from the exobase Earth s upper atmosphere is rich in O 2 (a good EUV absorber) and poor in CO 2 (a good IR radiator) the exosphere is hot T 700 K (solar min) 1200 K (solar max) Furthermore, H 2 is broken apart into H atoms by reaction with hot O atoms H 2 + O H + OH OH + O O 2 + H Escape of light H atoms is therefore relatively easy

Thermospheric temperature profiles for Earth T n T i T e T n T i T e Solar minimum T n = neutral temperature T i = ion temperature T e = electron temperature Solar maximum F. Tian, J.F. Kasting, et al., JGR (2008)

Hydrogen escape from the exobase For Earth, there are 3 important H escape mechanisms: Jeans escape: thermal escape from the high-energy tail of the Maxwellian velocity distribution Charge exchange with hot H + ions in the magnetosphere The polar wind Let s consider Jeans escape first

Kinetic theory of gases Jeans escape is a form of thermal escape. Jeans theory relied on previous work by Maxwell James Clerk Maxwell (1831-1879) (The work of Maxwell)... the most profound and the most fruitful that physics has experienced since the time of Newton. Albert Einstein, The Sunday Post Image from Wikipedia

Maxwellian velocity distribution Let f(v) be the number of molecules with speeds between v and v + dv Constants: k = Boltzmann s constant, 1.38 10-23 J/K m = molecular mass T = temperature (K)

Kinetic theory of gases Sir James Jeans (1877-1946) Wrote: The Dynamical Theory of Gases (1904) Figured out large chunks of what we now study in physics classes Image from Wikipedia

Jeans (thermal) escape H atoms with velocities exceeding the escape velocity can be lost v esc

Escape velocity In order to escape, the kinetic energy of an escaping molecule must exceed its gravitational potential energy and it must be headed upwards and not suffer any collisions that would slow it down Who can do this mathematically?

Escape velocity ½mv 2 e = GMm/r (K.E.) (P.E.) v e = (2 GM/r) 1/2 = 10.8 km/s (at 500 km altitude) m = mass of atom (1.67 10-27 kg for H) M = mass of the Earth (5.98 10 24 kg) G = universal gravitational constant (6.67 10-11 N m 2 /kg 2 ) r = radial distance to the exobase (6.871 10 6 m)

Most probable velocity v s H atoms with velocities exceeding the escape velocity can be lost v esc

Root mean square velocity Energy: ½ kt per degree of freedom Translational energy: 3 degrees of freedom KE = 3/2 kt ½ mv 2 = 3/2 kt v rms = (3 kt/m) 1/2

Most probable velocity Most probable velocity: v s = (2 kt/m) 1/2 Evaluate for atomic H at T = 1000 K v s = 4.07 km/s Compare with escape velocity v esc = 10.8 km/s These numbers are not too different an appreciable number of H atoms can escape

Escape parameter, Define the escape parameter, c, as the ratio of gravitational potential energy to thermal energy at the critical level, r c c = GMm/r c = GMm/r c ½mv2 s ½m (2kT/m) c = GMm ktr c

Jeans escape flux The Jean s escape velocity can be calculated by integrating over the Maxwellian velocity distribution, taking into account geometrical effects (escaping atoms must be headed upwards). The result is The escape flux is equal to the escape velocity times the number density of hydrogen atoms at the critical level, or exobase esc = n c v J

If the exospheric temperature is high, then Jeans escape is efficient and hydrogen is easily lost In this case, the rate of hydrogen escape is determined at the homopause (diffusionlimited flux) If the exospheric temperature is low, then hydrogen escape may be bottled up at the exobase

Hydrogen escape processes Mars and Venus have CO 2 - dominated upper atmospheres which are very cold (350-400 K) Escape from the exobase is limiting on both planets

Venus dayside temperature Upper atmosphere is relatively cool, despite being strongly heated by the Sun CO 2 is a good infrared radiator, as well as absorber profile http://www.atm.ox.ac.uk/user/fwt/webpage /Venus%20Review%204.htm

Hydrogen escape processes For Earth, Jeans escape is efficient at solar maximum but not at solar minimum However, there are also other nonthermal H escape processes that can operate..

Nonthermal escape processes Charge exchange with hot H + ions from the magnetosphere H + H + (hot) H + + H (hot) The New Solar System, ed., 3, p. 35

Nonthermal escape processes The polar wind: H + ions can be accelerated out through open magnetic field lines near each pole The upward acceleration is set up by a charge separation electric field that exists in the ionosphere Electrons are lighter than the dominant O + ions; hence, they tend to diffuse to higher altitudes http://www.sprl.umich.edu/sprl/research /polar_wind.html

Conclusion: Hydrogen can escape efficiently from the present exobase at both solar maximum and solar minimum H escape is limited by diffusion through the homopause Corollary: The escape rate is easy to calculate (see next lecture)