Carotene retention in vegetable leaf meals depends primarily on the storage temperature. Of the three temperatures used in these tests (So, 24", and 37.5" C.), the greatest carotene stability was at 5" and the least at 37.5'. Retention varied with the species of leaf, and a high oxalic acid content of the leaf seemed to be favorable. Carotene concentrates from leaf meals dissolved in oils are more stable than crystalline carotene in the same oils, possibly owing to the tocopherol i s the Concentrate. Levels of carotene up to 1000 micrograms per gram are more stable than the 5000-and 15,000-microgram levels. Oil solutions of carotene, of w-hatever source and at any concentration, are in most cases more stable at 5" C. than at higher temperatures. Addition of d-isoascorbyl palmitate and soybean lecithin to the carotene solution is ineffective in reducing loss of carotene.ERTAIN dry vegetable leaf meals can be prepared which C contain large amounts of carotene ( 6 ) . These meals can be used as poultry feed supplements (15) or as starting material for carotene concentrates (18). Since both the leaf meals and oil solutions of the carotene concentrate may often be held in storage for considerable periods, the carotene losses of these products under various storage conditions were investigated.Leaves of beet, carrot, broccoli, lima bean, rhubarb, spinach, and sweet corn were dried to a residual moisture content of 5% and ground 30 t o 40 mesh in a Wiley mill. Prior t o drying, portions of each material were blanched with steam at 100" C. or hot water at 90" to 100" for 5 minutes. The ground leaf meals were stored in 4-ounce screw-capped bottles; some were also stored in cloth bags. The meals were kept in the dark at 5 ", 24", and 37.5' C. A carotene concentrate was prepared from a mixture of a number of leaf meals. The mixture was extracted with Skellysolve B; the extract was saponified to remove chlorophyll, and finally purified with hydrated lime according to the procedure of Wall, Kelley, and Willaman (18). Removal of the solvent gave the carotene concentrate used for all the "concentrate" experiments.Aliquots of the concentrate, dissolved in Skellysolve B, were mixed with crude soybean and peanut oils; refined cottonseed, corn, soybean and peanut oils; lard, Crisco (a commercial shortening made from hydrogenated vegetable oil), and mineral oil. Aliquots were taken to give 100, 1000, 5000, and in some cases 15,000 micrograms of carotene per gram of oil. The solvent was removed on a warm water bath under nitrogen and vacuum. The oil solutions were stored in screw-capped vials in the dark at 5 O, 24", and 37.5 O C. I n the concentration range 100 to 5000 micrograms, 5 grams of oil solution were stored in 60 X 17 mm. vials. A t the 15,000-microgram range concentration, 2 grams of oil solution were stored in 45 X 15 mm. vials. Samples were analyzed for carotene over a period of 6 months, using single determinations. Similar studies were made with oil solutions of crystalline carotene prepared in the same manner as the c...