Little information is available on the oxygen consumption of specific portions of the central nervous system during their initial stages of embryonic development (1, 2). The spinal cord motor horns of chick embryos are well suited for such a study since their development has been well described (3)(4)(5)(6)(7)(8)(9)(10)(11)(12)(13)(14)(15). Therefore, in order to follow changes in the respiration rate of a neural tissue as it develops from neuroepithelium into arrays of neurons we measured the oxygen consumption of fragments of the anterior motor horns of chick embryo spinal cords at various stages of development.Methods. Fertile white Leghorn eggs were obtained from the Poultry Science Department, University of Saskatchewan, and were incubated at 38" until the desired embryonic stages (16) were reached, i.e., stages 11 k 1, 17, 26 =t 1, 36, and 42 (approximately 13i, 255, 5 , 10, and 16 days of incubation, respectively). The embryos were removed from the eggs, placed in Hanks' balanced salt solution and carefully staged. Under a dissecting microscope the spinal cord, brachial or presumptive brachial level, was dissected out of the embryo and transferred to incubation medium (150 m M NaC1; 3.0 m M KCl; 1.7 m M KH2P04; 8.0 m M Na2HP0,.7H20; 1.0 m M CaC12 .2H20; 0.6 m M MgCl,; 7 m M D-glucose; pH = 7.4, 327 mOsm per kg water) lying over 2 % "Special Agar-Noble" (Difco). Small cubes averaging approximately 10 X lo5 pm3 in size (range 5-30 X lo5 pm3) were cut out of the motor horns, or presumptive motor horns (see Fig. 1) by pressing finely sharpened tungsten needles through the cord into the agar. The actual dimensions of each cube were measured by means of a This work was supported by grants from the Medical Research Council of Canada (M.R.C.) to Drs.