The koala is the most specialized of the Australian marsupials, its diet being confined to certain species of eucalyptus leaves. Some years ago it was in danger of extinction but active conservation has saved it and it is still highly protected. Permission granted by the Fisheries and Wildlife department allowed us to investigate adrenal secretory function in one animal, a male weighing 7\m=.\5 kg.Anaesthesia was induced with ether and maintained by an i.v. infusion of sodium pentobarbitone. The adrenal venous collections were made as previously reported (Weiss & McDonald, 1965). Procedures for isolation, characterization and quantitative assay of steroids are described in previous publications (Weiss & McDonald, 1967;Weiss, 1968). Additional procedures employed were: (1) thin-layer chromatography on silica gel G (Stahl) in systems chloroform:ethyl acetate (1:50), chloroform: n-hexane (1: 10); (2) gas chromatography of 17 keto-and 21 deoxy-steroids using a model 402 F and M instrument with a glass column and 5 % SE-30 packing, temp. 230°C , nitrogen gas flow 35 ml/min, the quantitative measurements being made by using standard steroids and internal markers and measuring the relative peak areas, and (3) the basic double isotope method of Kliman & Peterson (1960) was used for aldosterone assay but substituting the chromatography systems with the LB 53/80 and L/80 (for 40 h) (Bush, 1961), TLC benzene : ethyl acetate (1:10) and 66% methanol on mesitylene-impregnated paper. The specific activity of [4-14C]aldosterone was 15 mCi/mmol and of acetic anhydride-T, 100 mCi/mmol. The combined adrenal glands gave a low ratio of 49 mg adrenal tissue/kg body weight, which is in the range reported by Bolliger (1953), who found an average of 68 mg/kg body weight in three koalas. Ten steroids were isolated and identified from adrenal venous blood, namely cortisol, corticosterone, aldosterone, 21-deoxycortisol, 11-deoxycortisol, ll/?-OH progesterone, 17a-0H progesterone, ll/?-OH androstene¬ dione, A4-androstenedione and progesterone. All showed the characteristics of a 4-3 oxo group, and their Chromatographie mobilities and retention times matched the appropriate reference steroid both before and after acetylation and oxidation. The reactions given by the biological extracts with blue tetrazolium, Porter-Silber and Zimmermann reagents were identical to those obtained with authentic reference steroids. Except for aldosterone, a sulphuric acid spectrum was obtained from each of the reported steroids and these matched exactly the spectra of authentic steroids.Two collections of adrenal venous blood were taken, one before and the second during corticotrophin (ACTH) infusion. Porcine ACTH was infused at a rate of