We report the results of inorganic carbon (C) uptake experiments and activity measurements for carbonic anhydrase, ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco), and phosphoenolpyruvate carboxylase (PEPC) in offshore and coastal regions of the eastern subarctic Pacific Ocean. HCO 2 3 was the dominant source of inorganic C taken up by phytoplankton at all sampling locations, accounting for ,60-90% of total C uptake. The uptake of HCO 2 3 occurred primarily through a direct transport system, while indirect HCO 2 3 use, mediated by extracellular carbonic anhydrase (eCA), played a minor role in the C uptake system. Direct HCO 2 3 transport and eCA activity were not related to ambient nutrient or CO 2 concentrations or to phytoplankton biomass (chlorophyll a [Chl a]) or primary productivity. There was significant variability in the biomass-normalized activities of Rubisco, PEPC, and total (intracellular and extracellular) carbonic anhydrase. The activities of all of the enzymes measured exhibited significant correlations with both CO 2 concentrations and Chl a. PEPC activity averaged 20% of Rubisco activity (range 0.5-110%), and the PEPC : Rubisco ratio was positively correlated with CO 2 concentrations and negatively correlated with Chl a. Carbonic anhydrase activity was strongly anticorrelated with CO 2 and positively correlated with Chl a. The results provide evidence for the importance of CO 2 -regulated carbon concentrating mechanisms in marine waters.Laboratory studies have documented the existence of inorganic carbon concentrating mechanisms (CCMs) in a variety of marine algal and cyanobacterial species (see Kaplan andReinhold 1999, andColman et al. 2002 for recent reviews). Although the molecular pathways have not been fully resolved, it is clear that CCMs enable cells to saturate carbon (C) fixation by ribulose 1,5-bisphosphate carboxylase/oxygenase (Rubisco) despite the poor catalytic efficiency of this enzyme (Spreitzer and Salvucci 2002) and the relatively low CO 2 concentrations in seawater. The CCM consists of a high affinity uptake system for inorganic C and the intracellular accumulation of CO 2 in the vicinity of Rubisco. Many phytoplankton species appear to use the abundant HCO 2 3 ion as a C source, through either a direct transport system or an indirect uptake pathway in which carbonic anhydrase (CA) catalyzes the otherwise slow dehydration of HCO 2 3 to CO 2 in the cell boundary layer (Sü ltemeyer et al. 1993;Badger 2004). Recent evidence also suggests that some phytoplankton species may possess a C 4 photosynthetic pathway in which intracellular HCO 2 3 is converted to an organic acid via phosphoenolpyruvate carboxylase (PEPC), and CO 2 is subsequently liberated by decarboxylation in close proximity to Rubisco (Reinfelder et al. 2000). By regulating the activity of the C transport system, Rubisco, carbonic anhydrase, and potentially PEPC, phytoplankton species may optimize growth over a wide range of ambient CO 2 concentrations.While laboratory experiments have provided detai...