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cascades. Interspersed amongst this structure are broad sandbars <br />and other depositional features more typical of erosive <br />southwestern streams. These shift seasonally (and dramatically) <br />according to duration and extent of flooding. Dominant riparian <br />vegetation is a mixture of native [Catclaw acacia (Acacia <br />greggii), Honey mesquite (Prosopis qlandulosa), Coyote Willow <br />(Salix exigua), Arrowweed (Tessaria sericea)), and nonnative <br />species [Tamarisk (Tamarix chinensis), Camelthorn (Alhagi <br />camelorum)) (Carothers and Brown, 1991; Johnson, 1991). Giant <br />reed (Phragmites australis) and cattail (Typha spp.) occur <br />patchily. The lower LCR passes through a narrow gorge that <br />progressively widens and deepens as it drops towards Marble <br />Canyon. A series of precipitous travertine falls at RKM 14.9 <br />(Atomizer Falls, Fig. 1--2b) mark upstream distribution of G. <br />cypha. <br />Base camps.---Three base camps were established in the LCR gorge: <br />Near its confluence (RKM 0.55); at Powell Canyon (RKM 3.1); and <br />at Salt Canyon (RKM 10.8). Biologists worked from each camp. <br />Those at the confluence fished the lower 1.2 km of river, while <br />those at Powell camp fished upriver from 1.3--7.0 km. Salt camp <br />personnel fished from 8.0--14.9 km. <br />Data collection.---Fishes were captured during 19 6--14 day trips <br />at approximately monthly intervals from July 1991 to December <br />1992. Hoop nets (0.76 or 1.2 m dia., 2.4 or 3.0 m length, four- <br />or six-hoop, single- or double-throat) were deployed in all <br />available habitat types of sufficient depth (i.e., > 0.4 m). <br />Trammel nets (7.6 to 45.7 m length, 1.8 m depth, 1.3 to 3.8 cm <br />inner and 30 cm outer meshes) were set routinely in the <br />confluence. Fishing effort for a particular trip was recorded as <br />number of net-hours per camp. <br />All captured fishes were identified, measured (TL to nearest <br />mm) and weighed (nearest g). Native species were examined for <br />tags, markings, secondary sexual characteristics, ripeness, and <br />general health and condition. Those greater than 150 mm TL <br />'adults') were injected with passive integrated transponder <br />(i.e., PIT) tags (see Prentice et al., 1990) and released near <br />points of capture. Nonnative fishes were scanned for presence of <br />PIT tags (a result of consuming tagged native fishes), then <br />sacrificed and either dissected immediately or preserved for <br />later study. <br />Analytical protocol.---One-way ANOVA (Proc GLM; SAS, 1985) was <br />used to compare total fishing effort and captures of adult G. <br />cypha by reach and year. To determine movements during 1992 <br />(which represented a full year of sampling), adult chubs were <br />grouped by reach and season (winter = December, January, <br />February; spring = March, April, May; summer = June, July, <br />August; and autumn = September, October, November). Numbers of G. <br />cypha tagged/recaptured in a given reach during a given trip were <br />3