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ecosystem dimension (i.e., catchment size) is logically determined by the question <br />being examined or the resource being managed. <br />The time frame encompassing the research question or management problem is <br />of course also important. In geologic time, as a result of orogeny and erosion, <br />watersheds were bisected and catchments reorganized, which clearly had enormous <br />zoogeographic consequences (Stanford and Ward 1986). In a much shorter time <br />frame, engineering projects artificially connected catchments via trans-watershed <br />diversions of rivers in many areas (Stanford and Ward 1979; Davies and Walker 1986), <br />allowing differently adapted organisms to comingle (Guiver 1976) or greatly <br />accelerating immigration of nonnative biota introduced by other means (Stanford and <br />Ward 1986, Mooney and Drake 1986). <br />Given that catchments may be referred to as ecosystems and that the ecosystem <br />is dynamic in time and space as well as in its relation to environmental problem <br />solving, it is fundamentally important to recognize the major structural features and <br />dimensions of river ecosystems (Figure 1). Ecologists have appreciated for many years <br />the importance of microhabitats encompassed by the run-riffle-pool sequence as <br />influential on the distribution and abundance of biota within the river channel. Zonation <br />of biota within the longitudinal continuum has long been recognized as a fundamental <br />feature of the lotic environment (Hynes 1970), although mechanisms explaning <br />specific distribution patterns often remain contentious (Alstad 1982, 1986, Thorp et al. <br />1986). Within the last decade, the connection between riparian zones, including the <br />surficial floodplain dynamics, and ecological structure and function has been clearly <br />demonsrated (see reviews in Dodge 1989, Gregory et al. in press). Microbial <br />transformation and transport of solutes in groundwaters has been shown to be an <br />important source of plant growth nutrients for channel biotopes in streams (Stanford <br />and Ward 1988, Ford and Naiman 1989, Dahm et al. 1990, Stream Solute Workshop <br />1990, Grimm et al. in press, Valett et al. in press); and, penetration of groundwaters <br />(i.e., the hyporheic zone, Figure 1) by amphibiotic stream biota has been documented <br />(Schwoerbel 1967, Stanford and Gaufin 1974, Williams and Hynes 1974, Bretschko <br />1981, Danielopol 1984, Pugsley and Hynes 1986, Stanford and Ward 1988). But, the <br />presence of large-scale hyporheic zones and the critical importance of groundwater - <br />surface water interchange as a major landscape feature of catchments has only <br />recently been demonstrated (Stanford and Ward 1988, Danielopol 1989, Gibert et al. <br />1990). <br />River floodplains are often, if not always, penetrated by interstitial, subterranean <br />flow (Figure 2). Water penetrates (downwells) at the upstream end of the floodplain, <br />5