SWAS data show that in the Orion Molecular Cloud, gaseous water and
O2 are not the main reservoirs of elemental oxygen. Their
abundances account for much less than 1% of the total abundance of
oxygen; the total is constrained by observations of diffuse clouds
where the fractional abundance of all the oxygen not locked in grains
(in silicates) is of the order of 3.2 10-4. In
dense regions of interstellar space, however, a large portion of the
oxygen is found on grains as water ice.
Contrary to model predictions (e.g. Maréchal et al. 1997),
the SWAS results also indicate that O2 and H2O are not the major
coolants in general for molecular clouds, although in some localized
regions, such as shocked, hot regions, ISO has shown that the
gas-phase fractional abundance of water can be as high as 10-4 (Harwit et al. 1998; Nisini et al. 2000).
Bergin et al. (2000) summarized the constraints yielded by SWAS and ISO as follows:
The constraints imposed by SWAS (and ISO) represent a challenge for theorists. Why do simple models predict large abundances at steady-state for gaseous H2O and O2? Where is the oxygen in quiescent clouds, and in regions of low-mass and high-mass star formation? Chemical models must self-consistently reproduce: (i) the gas-phase molecular oxygen and water abundances observed with SWAS; (ii) the water ice abundance measured with ISO; (iii) the abundances of simple and complex oxygen and carbon bearing species observed with ground based telescopes, and (iv) the observed abundances in a variety of different environments such as regions of high and low mass star formation and starless cores. We note, however, that the SWAS beam is as large as 4 arcmin and that the SWAS observations inevitably encompass a variety of interstellar and circumstellar regions; in effect, the SWAS results give averages over a variety of conditions.
In this paper we explore two theoretical approaches which may provide solutions to the constraints imposed by SWAS while still satisfying the constraints of observations of other simple and complex species. Section 2 is dedicated to the first approach: we investigate time-dependent models where gas phase species are allowed to deplete on to the grains. Bergin et al. (2000) showed that the SWAS data can be explained with low temperature gas phase models only if the observed clumps are short-lived, and we explore this point in detail. We show that "transient" states in which the chemistry satisfies constraints arising from SWAS and other observations are very long-lived in models where most species freeze-out efficiently on to dust grains except for CO and N2 which are returned promptly to the gas phase. Section 3 concerns the applicability of bistability solutions to the interpretation of the SWAS results. The gas phase chemistries discussed in Sects. 2 and 3 are identical. Section 4 presents a discussion of our findings.
Copyright ESO 2001