When microbes are subjected to temporal changes in nutrient availability, growth rate and substrate affinity can contribute to competitive fitness and thereby affect microbial community structure. This hypothesis was tested using planktonic bacterial communities exposed to nutrient additions at 1-, 3-, 7-, or 14-day intervals. Growth rates after nutrient addition were inversely proportional to the pulse interval and declined from 0.5 h ؊1 to 0.15 h ؊1 as the pulse interval increased from 1 to 14 days. The dynamics of community structure were monitored by 16S rRNA gene PCR-denaturing gradient gel electrophoresis. At pulse intervals of more than 1 day, the community composition continued to change over 130 days. Although replicate systems exposed to the same pulse interval were physiologically similar, their community compositions could exhibit as much dissimilarity (Dice similarity coefficients of <0.5) as did systems operated at different intervals. Bacteria were cultivated from the systems to determine if the physiological characteristics of individual members were consistent with the measured performance of the systems. The isolates fell into three bacterial divisions, Bacteroidetes, Proteobacteria, and Actinobacteria. In agreement with community results, bacteria isolated from systems pulsed every day with nutrients had higher growth rates and ectoaminopeptidase specific activities than isolates from systems pulsed every 14 days. However, the latter isolates did not survive starvation longer than those provided with nutrients every day. The present study demonstrates the dynamic nature of microbial communities exposed to even simple and regular environmental discontinuities when a substantial pool of species that can catabolize the limiting substrate is present.In most natural ecosystems microorganisms are likely to experience alternating periods of unrestricted growth with surplus nutrients, nutrient-limited growth, and starvation (6, 35). For example, phototrophs are exposed to light-dark cycles (23), with resulting effects on substrate supply to heterotrophs (1). These nutrient pulses can take place at all scales in nature (36)-over kilometers in coastal marine upwellings (19) and millimeters in laminated microbial mats. For heterotrophic microorganisms, the availability of organic substrates as the carbon and energy source is probably the most significant environmental restriction on growth (24). This is particularly true in unsaturated soil habitats, where nutrient mobility is restricted and surface-attached bacteria may remain dormant for extended periods (6).The interval between nutrient pulses could have substantial effects on microbial community composition and perhaps on microbial community function. When a nutrient pulse recurs, the physiological traits that are selected may be in opposition to those required for the microbes to survive an extended period of starvation. The exposure of a starved community of bacteria to an energy source results in interspecies competition (9) and was predicted to s...