A&A 413, 373-380 (2004)
DOI: 10.1051/0004-6361:20031515
O. Mousis
CNRS-UMR 6091, Observatoire de Besançon, BP 1615, 25010 Besançon Cedex, France
Received 9 January 2003 / Accepted 12 September 2003
Abstract
We study the thermodynamical conditions existing in the
Uranian subnebula from which the regular satellites were presumably
formed, assuming it was produced by an earth-sized body impact on
proto-Uranus (Stevenson 1984; Slattery et al. 1992). Two evolutionary
turbulent models of the Uranian subnebula are constructed. Both are derived
from the solar nebula analytical model of Dubrulle (1993) and Drouart
et al. (1999). Each model provides a distinct chemical composition which
depends on the assumed origin of the subdisk's material (proto-Uranus or
impactor ejected material). Moreover, the evolution of the chemistry of C
and N compounds is examined in order to assess the nature of major volatiles
trapped into the ices of regular satellites. The temporal evolution of the D/H
ratio in water is also explored in the Uranian subdisk, as a function of
the gas phase composition. Such an analysis may provide constraints on the
origin of the material which led to the formation of the regular satellite system.
Key words: planets and satellites: Uranus - solar system: formation - accretion, accretion disks
Table 1: Major regular satellites radii, densities, and per mass ice/rock ratios derived from Brown et al. (1991).
In this paper, the 1D solar nebula analytical model elaborated by Dubrulle (1993) is used to investigate the thermodynamical conditions existing in the protosatellite accretion disk surrounding Uranus, assuming it was produced by a giant collision. Given the uncertainties on the origin of the material forming the Uranian subnebula (proto-Uranus or impactor originating material), we consider two turbulent models which provide different chemical compositions. These models allow us to explore the evolution of carbon and nitrogen gas-phase chemistries in the Uranian subnebula and to deduce the nature of C and N volatiles trapped in icy planetesimals from which the regular satellites were presumably formed. The evolution of the D/H ratio in the vapor phase of water is also examined in the Uranian subnebula. Indeed, since it strongly depends on the chemical composition of the subdisk, such an analysis is likely to provide constraints on the origin of the material that formed the Uranian satellites.
The outline of the paper is as follows. In Sect. 2, a description of the structure and the evolution of the Uranian subnebula is given. Two different models, which provide different chemical compositions and thermodynamical parameters, are proposed. Section 3 is devoted to the investigation of the evolution of CO/CH4 and N2/NH3 ratios in both models of the Uranian subnebula. In Sect. 4, we discuss the trapping of C and N volatiles into the ices of the protosatellite disk. Section 5 is dedicated to the estimate of the D/H ratio in the water ice incorporated into regular satellites and its implications for the origin of the subnebula material. A summary is given in Sect. 6.
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In this study, two models of the Uranian subnebula are developed, each providing a different composition. The first model, hereafter labeled water-rich subnebula, is based on the conclusions of Slattery et al. (1992), who used hydrodynamic simulations to describe the evolution of the proto-Uranus and impactor system. Slattery et al. (1992) employed similar internal structure models, with respect to their sizes, for both proto-Uranus and impactor, which were derived from the interior models of Uranus developed by Hubbard & Marley (1989). We followed the prescription of Slattery et al. (1992), which consisted of selecting, among the dozens of results of their runs, those for which the rotation period of proto-Uranus consecutive to the impact is nearly similar to that of today. Most of the runs in compliance with this constraint revealed that the majority of the remaining orbiting material after the collision came from the impactor and was mainly composed of vaporized ices in orbit. Such a chemical composition of the initial gas phase of the Uranian subnebula should be close to that of the Oort comets. Indeed, since both Oort comets and the impactor are expected to be formed in the region of Uranus and Neptune, they probably shared a similar composition. Therefore, we infered from Iro et al. (2003) the abundances of major C and N molecules found in comets which could take part with H2O in the composition of the water-rich subnebula at t=0. In these conditions, CO, CH4, and NH3 gases are supposed to be the main C and N compounds in the subdisk, with abundances relative to H2O not exceeding 15% for CO, and 1.5% for both NH3 and CH4. Consequently, assuming that H2O was the major gas constituent, the gas mean molecular weight of the water-rich subnebula is about 18 g mole-1.
The second model, hereafter named water-poor subnebula, is based on the hypothesis of a blowout disk engendered by the giant collision, where a part of the giant planet's envelope was ejected into orbit to produce a satellite disk. In the blowout disk scenario proposed by Stevenson (1984), the H2-He-CH4-H2O atmosphere of proto-Uranus was shocked, involving the complete chemical conversion of the expelled methane into carbon monoxyde. As a consequence of this conversion, some oxygen was associated with carbon and reduced the quantity of water in the subnebula. Furthermore, assuming that NH3 exists in solar proportions in the atmosphere of Uranus (Gulkis et al. 1978), its conversion into N2 also occurred in the expelled part of the envelope, as a result of the heating due to the shock (Pollack et al. 1991). Table 2 reflects the abundances of major species at t = 0 in the water-poor subnebula which were inferred from the atmosphere of Uranus. The He/H2 ratio is deduced from Voyager measurements (Conrath et al. 1987). According to Baines et al. (1993), carbon is enriched 32 times compared to its solar value in the atmosphere of Uranus. Since O/H has never been measured in the atmosphere of Uranus, oxygen is conservatively assumed to be enriched, compared to its solar value, by the same factor as carbon. Such a composition leads to a mean molecular weight of 3.1 g mole-1 for the water-poor subnebula.
Table 2: Per volume abundances of He, O and C elements in the water-poor Uranian subnebula. He, CO, and H2O are the dominant species with hydrogen gas in the water-poor subnebula.
Table 3: Thermodynamical parameters of the water-rich and water-poor subnebulae.
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Figure 1:
Temperature profiles throughout the water-rich subnebula characterized by
the parameters
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Figures 1-3 exhibit radial profiles of temperature T, pressure P, and surface
density
respectively, at various epochs throughout the water-rich subnebula. Radial profiles of T, P and
are similar for the water-poor subnebula, even if its radius is more
extended than that of the water-rich subnebula. In both models, water remains in vapor phase at
t = 0 and T, P, and
decrease with time and with the uranocentric distance. The
cooling of the water-rich subnebula allows the propagation front of crystalline water to reach
the orbits of Oberon (22.3
), Titania (16.6
), Umbriel (10.1
),
Ariel (7.3
), and Miranda (5
)
at
,
,
106,
,
and
years. In the case of the water-poor
subnebula, crystalline water condenses at the same orbits at
,
,
,
,
and
years.
Both water-rich and
water-poor Uranian subnebulae display structures similar to those detailed by Mousis et al. (2002a)
and Mousis & Gautier (2003) for the Saturnian and Jovian subdisks. Figure 4 shows, as a function of time, the mass of gas and planetesimals contained in a ring of one
width in the water-poor subnebula, centered at a distance R of Uranus.
This figure illustrates that, at each time, gas and planetesimals are mainly located in the
outer part of the subdisk. This remark is also valid for the water-rich subnebula.
In fact, such structures demand that the zone of formation of regular satellites
was fed by planetesimals that migrated inwards from the outer part of the subnebula (Coradini et al. 1989).
Indeed, following the mechanism invoked by Makalkin et al. (1999) in the case of the
formation of Galilean satellites,
the high efficiency of the capture of particles by the growing satellite embryos may have
led to the accumulation of solid material on the orbits of regular satellites in the subdisk.
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Figure 2: Pressure profiles throughout the water-rich subnebula characterized by the same parameters as in Fig. 1, for various values of t in years. |
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Figure 3: Surface density profiles throughout the water-rich subnebula characterized by the same parameters as in Fig. 1, for various values of t in years. |
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Figure 4: Mass distribution in the water-poor subnebula as a function of time. Most of the mass is in the outer part of the subnebula. |
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In the case of the water-poor subnebula, its hydrogen-dominated medium required us to check
the possibility of CO
CH4 and N2
NH3 conversions.
The gas phase chemistries of carbon and nitrogen in media dominated by H2 are represented
in Figs. 5 and 6, respectively. At equilibrium, CO/CH4 and N2/NH3 ratios depend only
upon local conditions of temperature and pressure
(Prinn & Barshay 1977; Lewis & Prinn 1980; Smith 1998).
CO/CH4 and N2/NH3 ratios of 1000, 1, and 0.001 are plotted in Figs. 5 and 6, and compared to the water-poor subnebula at t = 103,
104, and 105 years. On these figures, it can be seen that at early epochs and if the kinetics
of chemical reactions are ignored, CO and CH4, and N2 and NH3 exist together in the water
poor subnebula. With time, the part of the subnebula where CH4 and NH3 dominate increases,
as it is indicated in Figs. 5 and 6.
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Figure 5:
Calculated ratios of CO/CH4 in the water-poor subnebula at equilibrium. The solid
line labelled CO-CH4 corresponds to the case in which the abundances of the two gases are equal.
When moving towards the left side of the solid line, CO/CH4 increases, while when moving
towards the right side of the solid line, CO/CH4 decreases. The dotted contours labelled -3, 0,
3 correspond to log10 CO/CH4 contours. Adiabats of our turbulent model of the
Uranian subnebula are calculated at three epochs. The origin of time corresponds to the moment when the
giant impact occured. The uranocentric distance, in
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Figure 6: Same as in Fig. 5, but for calculated ratios of N2/NH3 atequilibrium. |
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Figure 7: Chemical times profiles calculated for CO/CH4 and N2/NH3 conversions in the water-poor subnebula. The conversion of CO to CH4 and of N2 to NH3 is inhibited in the subdisk, except quite close to Uranus. |
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However, taking into account the kinetics of C and N chemical conversions dramatically changes the
situation. Indeed, based on the appropriate kinetic data described by Smith (1998), we calculated
the chemical times that characterize the rates of
and
conversions by using the temperature and pressure radial profiles at different epochs of the
water-poor subnebula.
These calculations, illustrated by Fig. 7, show that, assuming C and N are initially entirely in the
forms of CO and N2 at t = 0 in the water-poor subnebula, their conversions into CH4
and NH3 can occur in a realistic timescale only quite close to Uranus and at early epochs. Considering the
structure of the disk where most of the mass is located in its cold outer part (see Fig. 4), one can argue
that the amount of CH4 and NH3 produced is too small to affect the initial abundances of CO and N2,
even if transport by turbulent diffusion is taken into account.
Thus, both models of the Uranian subnebula have preserved during their evolution the CO/CH4 and N2/NH3 ratios they initially acquired, as long as no condensation or trapping of these species occurred. The next step is now to examine how C and N volatiles were trapped in the ices of the Uranian subnebula and subsequently in the regular satellites.
During the cooling of the water-poor subnebula, most of CO and N2 was trapped by H2O ice
in the forms of CO-5.75H2O and N2-5.66H2O clathrate hydrates, respectively (Lunine &
Stevenson 1985; Davidson et al. 1987).
Figure 8 describes the temporal evolution of the crystallization radii of these ices throughout
the water-poor subnebula. At t = 0, H2O, CO and N2 remain in the vapor phase in the whole
subnebula.
The cooling of this medium allows the condensation of water to start at t = 103 yr at the
level of its outer edge. At this position, the trapping of CO and N2 by crystalline water
in the forms of clathrate hydrates begins at
yr and
yr.
With time, the condensation fronts of CO-5.75H2O and N2-5.66H2O clathrate hydrates propagate
inwards. The clathration of CO occurs at the current orbits of Oberon (22.3
)
and Miranda (5
)
at t = 0.4 Myr and t = 2.6 Myr, respectively. In turn, N2 is trapped by crystalline
water as a clathrate hydrate at t = 0.6 Myr and t = 4.2 Myr at the same orbits. This implies
that, in the case of the water-poor subnebula, the incorporation in planetesimals of CO and N2 in
the forms of clathrate hydrates should lead to the presence of important amounts of CO and N2 in
the interiors of regular icy satellites. The resulting C/N ratio in these bodies should reflect the
oversolar value present in the atmosphere of Uranus. Moreover, CH4/CO and NH3/N2 ratios should
be negligible in the satellite ices.
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Figure 8: Formation radii of water ice, CO-5.75H2O and N2-5.66H2O clathrate hydrates in the water-poor subnebula, as a function of time. The stability curve of N2-5.66H2O clathrate hydrate is calculated assuming that N/H is solar and all nitrogen is in the form of N2. The abundances of H2O and CO are given in Table 2. |
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A similar mechanism is invoked for the trapping conditions of C and N volatiles in the water-rich subnebula. Indeed, the cooling of this medium allows the formation of NH3-H2O hydrate, and CH4-5.75H2O and CO-5.75H2O clathrate hydrates at t = 0.42, 0.61 and 0.72 Myr respectively, at the current orbit of Oberon, if one assumes that NH3, CH4 and CO abundances are those prescribed in Sect. 2.2 for the water-rich subnebula. At the present orbit of Miranda, NH3-H2O, CH4-5.75H2O, and CO-5.75H2O never condense before t = 3.9, 5.6, and 6.6 Myr, respectively. This analysis implies that, in the case of the water-rich subnebula, CH4, CO, and NH3 should be the main C and N compounds trapped as hydrates or clathrate hydrates in the interiors of regular icy satellites. Furthermore, C/N should be oversolar in the satellite ices, since the trapping of C and N species in the water-rich subnebula must have preserved the initial mixing ratios.
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In the case of the water-poor subnebula, the situation is quite different. Indeed, in opposition to
the composition of the water-rich subnebula, hydrogen is the most important deuterium reservoir
in the subdisk. In addition, the D/H ratio in hydrogen must reflect the value measured in
the atmosphere of Uranus (
,
Feuchtgruber et al. 1999).
In these conditions, the evolution of f is
ruled by the equation of diffusion previously detailed by Drouart et al. (1999) and Mousis et al. (2000), which is:
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Equation (5) is valid as long as H2O does not condense. Indeed, the isotopic exchange
is inhibited between the vapor phase and the solid phase. This statement implies that
the value of the enrichment in microscopic ices is the one obtained at the time and at
the location of the condensation of vapor. As soon as grains reach the millimeter size,
they begin to decouple from gas, continue to grow, and form planetesimals. Whatever
the subsequent evolution of these bodies, their D/H ratio is that of microscopic grains.
In other words, the D/H ratio in H2O ices contained in the Uranian satellites is that
of these species when they condensed.
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Figure 9:
Calculated deuterium enrichment factor f in H2O as a function of Uranocentric
distance
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The enrichment factor f(R,t) is thus obtained by integrating Eq. (5), which requires spatial and
temporal boundary conditions. Spatial boundary conditions are determined by setting
= 0 at both
and
.
When condensation occurs within
,
we set
at the radius of condensation. Our scenario implies that,
at the time of the collision with the impactor, the temperature following the impact was high enough to
decompose in elements all the volatiles presents in the expelled material. This hypothesis seems
realistic since Stevenson (1984) described a shocked gas following impact reaching temperatures as
high as 104 K. Therefore, if the molecules have been exclusively produced from the recombination of elements
in the initially hot water-poor Uranian subnebula, there is no initial fractionation between D/H ratios
in water and molecular hydrogen (f=1). Setting f(R) = 1 at t = 0 when integrating
Eq. (5) reveals that,
as shown in Fig. 9, f(R,t) would never exceed 1.3 at the level of the regular satellite system in the
life of the water-poor Uranian subnebula. This implies that water ice should not present a
deuterium enrichment greater than 4.4 times the protosolar value in the water-poor subnebula.
Finally, we have shown that the value of the D/H ratio in the water ice incorporated in regular satellites strongly depends on the primordial composition of the protosatellite disk. Subsequent in situ measurements of the D/H ratio in the ices of these bodies should provide constraints on the scenario which led to their formation. Indeed, if the measured deuterium enrichment in water ice, compared to the solar value, is close to that of Oort comets, it can be presumed that, as is shown by Slattery et al. (1992), most of the subnebula material came from the impactor. On the other hand, the measurement of a substantially lower deuterium enrichment in water ice would signify that most of the material came from a hydrogen-rich subnebula. Such an observation would comply with the blowout disk hypothesis defended by Stevenson (1984).
During their temporal evolution, both models of the Uranian subnebula have preserved the CO/CH4 and N2/NH3 ratios they initially acquired. In the case of the water-rich subnebula, assuming an initial gas phase composition close to that of Oort comets, CO, CH4 and NH3 should remain the major C and N compounds in the subdisk. In the case of the water-poor subnebula, as a consequence of the heating suffered by the expelled part of the giant planet's envelope composing the subdisk, CO and N2 should remain the main C and N compounds. In both models of the Uranian subnebula, C and N volatiles were trapped as clathrate hydrates or hydrates in planetesimals before they became incorporated into the regular satellites.
Furthermore, the evolution of the D/H ratio in water has been investigated in both models of the Uranian subnebula. It is shown that the resulting value of the D/H ratio in water ice taking part in the regular satellite composition is strongly dependent on the nature of the main reservoir of deuterated molecules existing in the subdisk's gas phase. In other words, this involves that future measurements of such a ratio in the regular satellite ices may constrain the origin of the subnebula which led to their formation.
Acknowledgements
Many thanks are due to Daniel Gautier for helpful discussions about this work. I wish to acknowledge Guy Moreels, Céline Reylé and Jean-Marc Petit for their valuable comments on the manuscript.