Summaryborn to healthy sows at known full term. All piglets were suckledPlasma volume and red cell mass of various organs in piglets aged 24 hr (n = 7) and 7 (n = 6). and 14 (n = 6) days were measured using eemTc-labeled albumin and "Cr-labeled red blood cells. Organ activities were counted in a whole-body counter. Blood volume and hematwrit were calculated. The blood volumes in $/g varied markedly between various organs. The lowest blood volumes at 24 hr of age were found in skin (21.9 + 5.0 pl/g), brain (33.3 ~t 8.4), and skeletal muscle (35.5 + 7.4). The highest values at this age were noted in liver (670.0 + 89.1), lung (533.8 f 80.7), spleen (332.0 + 82.8), and kidney (300.6 + 55.5). Blood volumes of about 150 pl/g were observed in heart muscle and thyroid gland and those of about 100 pl/g in thymus and gastrointestinal tract.The total blood volume was 100.2 * 3.9 pl/g at 24 hr and remained unchanged during the first 2 wk of life. A significant decrease in relative blood volume with growth was noted in liver and lung ( P c 0.01), and in skeleton ( P < 0.05). The blood volume, contained in the great vessels outside the organs, increased from 29.5 * 5.5% of total blood volume at 24 hr to 31.2 * 5.7% at 7 days and to 38.2 k 7.5% at 14 days of life. The total body/venous hematwrit ratio was about 0.84. Accordingly, tissue hematwrits of most organs were below the venous hematocrit. Only in spleen was the tissue/ venous hematwrit ratio (TH/VH) higher than 1.0. TH/VH of brain, gastrointestinal tract, thyroid gland, and thymus approached unity. The lowest TH/VH was found in kidney (0.54 f 0.08 at day 1). In skin, the TH/VH decreased from 0.98 * 0.10 to 0.82 * 0.07 during the first 2 wk of life.by their mothers. They were not treated 4 t i iron. The right atrium was cannulated with polyethylen catheters via the right external jugular vein for injection and withdrawal of blood. Each piglet received local analgesia with procaine at the site of catheterization, but no systemic drugs. Two ml of blood were withdrawn from the catheter and centrifu ed for 5 min at 1000 x g. The red R blood cells were labeled with chromium (17). Salt-poor human serum albumin (25%) was labeled by means of a commercial kit for electrolytic preparation of -technetium (New England Nuclear Corp., North Billerica, MA). Each preparation of *"Tclabeled albumin was carefully checked for particulate matter, turbidity, and pH (6). Labeling efficiency was determined with trichloracetic acid and membrane filtration (14). Batches containing more than 1% of unbound -Tc were discarded. One postmix blood sample of 1 ml was taken 10 min after injection of labeled red blood cells and 5 min after injection of labeled albumin. Previous equilibration studies have shown that mixing of red blood cells and of albumin are complete within that period (16). Loss of albumin from the intravascular space has been found negligible in this short time. The piglets were killed immediately after the labeling and blood collecting procedure by injection of 2 mval KC1 via the ca...