<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 />
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<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 />
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