The isothermal oxidation behavior of three alumina forming austenitic (AFA) stainless steels with varying composition was studied at 650 and 800°C in dry air and gases which contained water vapor. The AFA alloys exhibited better oxidation resistance than a ''good chromia former'' at 650°C, particularly in H 2 Ocontaining atmospheres by virtue of alumina-scale formation. Although the AFA alloys were more resistant than chromia formers, their oxidation resistance was degraded at 650°C in the presence of water vapor. In dry air the AFA alloys formed, thin continuous alumina scales, whereas in Ar-4%H 2 -3%H 2 O the areas of continuous alumina were reduced and Fe oxide-rich nodules and regions of Cr, Mnrich oxides formed. In some regions internal oxidation of the aluminum occurred in the H 2 O-containing gas. The alloy OC8 had slightly better resistance than OC4 or OC5 in this atmosphere. The alumina-forming capability of the AFA alloys decreases with increasing temperature and, at 800°C, they are borderline alumina formers, even in dry air. The oxidation resistance of all three alloys was degraded at 800°C in atmospheres, which contained water vapor (Air-10%H 2 O, Ar-3%H 2 O and Ar-4%H 2 -3%H 2 O). The areas, which formed continuous alumina, were reduced in these atmospheres and areas of internal oxidation occurred. However, as a result of the borderline alumina-forming capability of the AFA alloys it was not possible to determine which of the H 2 O-containing atmospheres was more severe or to rank the alloys in terms of their performance. The experimental results indicate that the initial microstructure of the AFA alloys also plays a role in their oxidation performance. Less protective oxides formed at 800°C when alloy OC8 was equilibrated before exposure rather than being exposed in the as-processed condition.