Tliis study attempted to 1) identify the metabolic pathways and enzymes involved in the photos>mthetic fixation of carbon and to determine 2) if metabolic intermediates were altered by changes in the supply of nitrogen and phosphorus; 3) if activity level of specific enzymes differed in tissue of superior and nonsuperior trees and their half-sibling seedling progeny; 4) if the activity was altered by the soils in which seedlings grew. Distribution of photoassimilated^^U02 measured in ethanolsoluble fractions of green tissue from 3-month-old Ocala sand pines grown from seed in sand culture and complete nutrient solutions containing two levels each of nitrogen and phosphorus. Portions of the metabolic pathways involved in carbon fixation were determined. Tlie activity and electrophoretic migration rate of malate dehydrogenase isoenz\nres, glucose-6-phosphate dehydrogenase isoenzymes, and proteins were compared in green tissue from saw log-size superior viii and neighboring, nonsuperior sand pine trees and their half-sibling progeny grown in pots on Lakeland coarse sand and Paola sand. Sugars contained 75%, organic acids 19%, and amino acids 6% of the radioactive carbon in the ethanol-soluble fraction from green tissue. Radioactivity was highest in fructose, glucose, and galactose. Nitrogen directly affected chlorophyll formation, seedling growth, and photosynthetic incorporation of 14c. Phosphorus appeared to be the principal rate-limiting element in the incorporation of carbon in sugars and in some organic acid precursors of amino acids. Results indicated that enzymes of glycolysis, the Calvin cycle, and the tricarboxylic acid cycle were principally involved in fixation of carbon in sand pine seedlings allowed to photoassimilate^^C 02 for 10 minutes in a controlled environment. Measurements of activity and migration of isoenzymes did not provide an index of growth superiority in parent trees or in halfsibling seedling progeny. Superior parent trees, but not their progeny, lacked one or more protein bands found in nonsuperior trees indicating that a genetic marker exists. However, no relationship was found between the location of malate dehydrogenase and glucose-6-phophate dehydrogenase isoenzymes and protein bands. Activity and Rf values of some malate dehydrogenase isoenzyme and protein bands were altered by the soil in which seedlings grew as well as by genetic factors. Both the isoenzyme and protein bands and factors influencing them were identifiable.