Sunmnmary. The products oif short time photosynthesis and of enlhanced dark 14CO2 fixation (illumination in helium prior to addition of 14CO, in dark) by Chlorella pyrenoidosa and Anacystis nidulans were compared. Glycerate 3-phosphate, phosphoenolpyruvate, alanine, and aspartate accounted for the bulk of the 14C assimilated dturing enhanced dark fixation while hexose and pentose phosphates accounted for the largest fraction of isotope assimilateed during photosynthesis. During the enhanced dark fixation period, glycerate 3-phosphate is carboxyl labeled and glucose 6-phosphate is predominantly labeled in carbon atom 4 with lesser amounts in the upper half of the C6 chain and traces in carbon atoms ; and 6. Tracer spread throughout all the carbon atoms of photo.synthetically synthesized glycerate 3-phosphate and glucose 6-phosphate. During the enhanced dlark fixation period, there was a slow formation of sugar phosphates which subsequently continued at 5 times the initial rate long after the cessation of 14C,O2 uptake. To explain the kinetics of changes in the labelling patterns and in the litmited formation of the sugar phosphates during enhanced dark C02 fixation, the suggestion is made that most of the reductant medi,ating these effects did not have its origin in the preillumination phase.I't is concluded that a complete photosynthetic carboni reduction cycle operates to a limited extent, if at all, in the dark period subsequent to preillumination.A current concept of photosynthesis postulates that a reductant generated in the light mediates the assimiliation of CO. through the "light independent" reactions of the reductive pentose ph-osphate cycle. If this is correct, then it should be possible to separate the overall process into 2 steps: the generation of the reductant in the light phase and its utilization in a subsequent dark period. Calvin and Bens,on (1, 2) showed that Chlorellat and Scenedesmus illuminated in an atmosphere of 100 % N2 (preillumination) were able to assiimilate briefly 1' CO. in the subsequent dark period at a rate higher than that of an unillu.minated sample. From analysis of the products of this enhanced dark "4CO2 fixation, which included labeled sugars, they concluded that both carboxvlation of an accumuilated CO2 acceptor and reduction of some of the subsequently labeled glycerate 3-P to the carbohydrate level to-ok place. They postulated the existence of a long lived reductant that survived into the dark period. Ba,ssha'm and Kirk (3) reported a rapid and parallel incorporation of tracer into glycerate-3-P and hexose monophosphate dulrinlg enhanced (lark '4CO., fixation following a period of photosynthesis. These workers envisaged the generation of long lived reducing power along with ribbulose 1,5-diP during the period of illuminatioil ani(I the conversion of -"CO. to carbohydrate in the dark through the reactions of the photosynthetic carbo-n redtuction cycle, mediated by this reducing power.Gaffron and co-workers (4, 5) investilgated the existence of enhanced dark "+C0O. fixat...