The abundance of individuals in microbial species is so large that dispersal is rarely (if ever) restricted by geographical barriers. This "ubiquitous" dispersal requires an alternative view of the scale and dynamics of biodiversity at the microbial level, wherein global species number is relatively low and local species richness is always sufficient to drive ecosystem functions.

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Published estimates of protozoan respiratory rates are reviewed with the object of clarifying their value in ecological studies. The data show a surprisingly large variance when similarly sized cells or individual species are compared. This is attributed to the range of physiological states in the cells concerned. The concept of basal metabolism has little meaning in protozoa. During balanced growth, energy metabolism is nearly linearly proportional to the growth rate constant; at the initiation of starvation, metabolic rate rapidly declines. Motility requires an insignificant fraction of the energy budget of protozoans. For growing cells, metabolic rate is approximately proportional to weight(0.75) and the data fall nearly exactly on a curve extrapolated from that describing the respiration rates of poikilotherm metazoans as a function of body weight. It is conceivable that protozoan species exist with lower maximum potential growth and metabolic rates than those predicted from cell volume and the equations derived from the available data. However, the lack of information concerning the state of the cells studied prevents verification of this idea. Laboratory measurements of protozoan respiratory rates have no predictive value for protozoa in nature other than delimiting a potential range. For small protozoans, this range may, on an individual basis, represent a factor of 50.

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We have quantified the bacteria, heterotrophic nanoplankton (HNAN), and other microorganisms in 108 lakes, ponds, rivers, and bogs worldwide. These water bodies span the range of biological productivities in freshwater. Numbers of HNAN and bacteria are correlated over four orders of magnitude in each (3 × 102 to 4 × 106 ml−1 and 3 × 105 to 1 × 109 ml−1, respectively) and both increase with the productivity of the water body. Most HNAN are small (2– 5 µm), colorless, flagellated protists. They grow at about the same rate as bacteria (µ = 0.01–0.02 h−1) and are capable of consuming the entire bacterial production. We suggest that bacterial abundances are regulated by substrate supply and HNAN grazing pressure. Ciliates and other grazing microzooplankton probably limit HNAN abundance, especially in the more productive water bodies. The structure and function of microbial food webs in freshwater environments may thus be similar to those suggested for marine systems.

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