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<br />, <br /> <br />.' <br /> <br />., <br /> <br />occupies a mid-column position or is pelagic. there may he <br />little difference hetween the mean column and nose veloci- <br />ties, However. simulation of mean column vehlCIlies for a <br />demersal species can have two detrimental results, First. <br />there will be an overall tendency for the amount of available <br />habitat to be underestimated for the higher flows. because <br />the mean column velocity will consistently be too fast for <br />the fish. Second, when usable microhabitat is plotted against <br />discharge, the resulting curve will peak at a relatively low <br />discharge, and will decrease rapidly at higher flows. Use of <br />nose velocities typically results in a more robust habitat vs. <br />discharge relationship (i.e., a broader curve) which may <br />peak at a higher flow than one based on mean column veloci- <br />ties. <br />We have avoided a definition of what differentiates a large <br />river from a small one. Many investigators would probably <br />make this distinction on the basis of channel width. mean <br />annual discharge, drainage area, or some other size-related <br />characteristic. Based on the foregoing discussion, the best <br />distinguishing characteristic may be channel depth, as this <br />will determine the vertical location of the mean column <br />velocity measurement. When measuring stream velocities, <br />as a rule of thumb, hydrologists change from a single mea- <br />surement at 0.6 of the depth to an average of two measure- <br />ments at 0.2 and 0.8 of the depth, when the depth exceeds <br />about 1 m. Therefore, it is suggested that whenever the <br />depth exceeds one meter, nose velocities be used instead of <br />mean column velocities, and that this is one criterion <br />differentiating small from large rivers. Based on this stan- <br />dard, there are relatively few small streams in North <br />America. <br />However, there is one other characteristic that distin- <br />guishes truly large rivers - the relative importance of <br />specialized or isolated habitat types associated with the river <br />margin. In small and medium-sized streams, the same spe- <br />cies is found at suitable locations throughout the stream. <br />There may be much more habitat partitioning in larger <br />rivers, with certain species associated only with edge <br />habitats, and others found almost exclusively in mid-stream. <br />It should be noted that this tendency is related more to the <br />combined effects of physical and hydraulic structure than to <br />the size of the channel. If a stream that would otherwise be <br />classified as large has the same structural diversity of a small <br />stream, the same species will probably be scattered through- <br />out the channel. However, many large rivers tend to have <br />a definite zonation, consisting of a hydraulically efficient <br />(and often biologically devoid) main channel, and the bio- <br />logically rich zones associated with the edges. In contrast, <br />the biologically rich zones tend to overlap in small rivers. <br />In many large rivers, the role of streamflow in the main <br />channel is little more than providing water to the zones <br />occupied by the fish. The determination and simulation of <br />flow-induced habitat fluctuations in these specialized habitat <br />areas provides the challenge in large-river investigations, <br />because of their tendency to be hydraulically controlled by <br />a variable backwater. The hydraulic complexities of these <br />areas can prove to be difficult to simulate, but are rarely <br />insurmountable. The more perplexing problem is that many <br />instream flow investigators do not (or cannot) recognize <br />variable backwaters when they see them. This emphasizes <br />the advantage of including expertise in hydraulics, hydrol- <br />ogy, and biology on any riverine habitat analysis team. <br />The determination of instream flow requirements to pro- <br /> <br />28 <br /> <br />vide suitable habitat for lishes can be assisted by use of <br />physical habitat versus srreamllow functions and the analy- <br />sis of instream benefits produced by alternative flow <br />regimes. These can be compared to benetits from diversion- <br />ar~ uses in order to obtain a reasonable mix of uses as the <br />!!~al of the allocation of the water resource. <br />~ If a habitat versus streamflow relationship is used as a sur- <br />rogate production function. a water management project can <br />be formulated to include instream flows as an equal among <br />various project purposes in the overall project production <br />function (MiIhous 1983). In contrast, if the function is used <br />only for the evaluation of impacts, the resulting instream <br />flow requirements are treated as constraints on the alloca- <br />tion of water to "useful" purposes (Henrikson 1980; Hoff- <br />man 1980; Christiano5). The use of the habitat-streamflow <br />function in a reservoir analysis was given by Milhous <br />(1982a), Sale et al. (1982), and Olive and Lamb (1984). <br /> <br />I <br />t <br />i <br />~ <br />I <br />t <br />i <br /> <br />f <br />1 <br />: <br /> <br />References <br /> <br />ANNEAR, T. C., AND A. L. CONDER. 1984. Relative bias of <br />several fisheries instream flow methods. N. Am. J. Fish. <br />Manage. 4: 531-539. <br /> <br />AMERICAN SOCIETY OF CIVIL ENGINEERS. 1962. Nomenclature of <br />hydraulics. ASCE manuals and reports on Engineering Prac- <br />tice No. 43. New York, NY. 501 p. <br />BAlDRIGE, J. E., AND D. AMOS. 1981. A technique for determin- <br />ing fish habitat suitability criteria: a comparison between hab- <br />itat utilization and availability, p.251-258. In N. B. <br />Armentrout [ed.] Acquisition and util ization of aquatic habitat <br />inventory information. Am. Fish. Soc., Bethesda, MD. <br />BINNS, N. A., AND F. M. EISERMAN. 1979. Quantification of flu- <br />vial trout habitat in Wyoming. Trans. Am. Fish. Soc. 108: <br />215-228. <br />BOVEE, K. D. 1982. A guide to stream habitat analysis using the <br />instream flow incremental methodology. Instream Flow <br />Information Paper No. 12. U.S. Fish Wild\. Servo <br />FWS/0BS-82/26. 248 p. <br />1985. Evaluation of effects of hydropeaking on aquatic <br />macro invertebrates using PHABSIM, p. 236-241. In F. W. <br />Olson, R. G. White. and R. H. Hamre [ed.] Proc. Symp. on <br />small hydropower and fisheries. Am. Fish. Soc., Bethesda, <br />MD. <br />1986. Development and evaluation of habitat suitability <br />criteria for use in the instream flow incremental methodology . <br />Instream Flow Information Paper No. 21. U.S. Fish Wildl. <br />Serv. BioI. Rep. 86(7): 235 p. <br />BRAY, D. I. 1982. Regime equations for gravel-bed rivers, <br />p. 517-542. In R. D. Hay, J. C. Bathurst, and C. R. Thorne <br />[ed.] Gravel-bed rivers. John Wiley and Sons, London. <br />BRUNGS, W. A., AND B. R. JONES. 1977. Temperature criteria for <br />freshwater fish: protocol and procedures. U.S. Envi- <br />ronmental Protection Agency, Ecol. Res. Series. <br />EPA-600/3-77-061. <br />BURNS, C. V. 1971. Kansas streamflow characteristics, Part 8, <br />In-channel hydraulic geometry of streams in Kansas. Kansas <br />Water Resour. Bd., Tech. Rep. 8. <br />CAIRNS, J., JR. 1%8. Suspended solids standards for the protec- <br />tion of aquatic organisms. Purdue Univ. Eng. Bull. 129(1): <br />16-27. <br /> <br />5 CHRISTIANO, D. J. 1981. Negotiating for instream water. <br />Presented at the 1981 Conference of the American Water Works <br />Association, St. Louis, MO, USA. <br />