IT was shown by Collee, Rutter and Watt (1971) that the difficulties encountered in the surface culture of Clostridium oedematiens (CZ. novyi) types B and D can be overcome by the use of modified Moore's medium (Moore, 1968) or by sprinkling sterile iron filings on the surface of a seeded blood agar plate. This approach made it possible to study quantitatively whether the growth was derived from spores or from vegetative cells. It was found for type D of this exacting organism that vegetative cells can account for an appreciable part of the growth obtained when a broth culture is subcultured on solid medium. This finding may be of practical importance also in the case of other anaerobes. It raises the question whether the traditional methods give adequate recovery of anaerobic organisms for clinical purposes or whether more elaborate procedures such as those of Hungate (1950) The following organisms were subcultured in nutrient broth after isolation from clinical material and identification : two strains of Staphylococcus aureus; one strain of Streptococcus pyogenes (group A), one strain of Bacillus anthracoides; one strain of Neisseria gonorrhoeae ; one strain of Veillonella sp.; and two strains of Haernophilus influenzae.Media. Cooked-meat broth was prepared as described by Cruickshank (1968, p. 757), but the infusion broth component was made from Nutrient Broth no. 2 (Oxoid). Oxoid Nutrient Broth was also used for the subculture of some of the test organisms. "Presteamed nutrient broth " was used as a diluent in the quantitative studies; it was heated by steaming at 100°C for 30 min. to remove dissolved air, then cooled rapidly to 37°C.In the initial studies, Watt's modification of Moore's medium (cysteine-dithiothreitol human blood agar) was used (Collee et ~1 . ) . In later studies, a further modification (cysteinedithiothreitol equine blood agar was prepared by substituting 10 per cent. horse blood for 33 per cent. human blood.Blood agar plates were prepared with Oxoid Blood Agar Base no. 2 enriched with equine blood (10 per cent.) or human blood (33 per cent.).Blood. Outdated citrated human blood was obtained from the Blood Transfusion Department, Edinburgh Royal Infirmary. Defibrinated equine blood was supplied by Wellcome Laboratories.