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may group into . differing levels of <br />degradation. Future studies need to <br />ascertain if this is true. The results also <br />suggest that chironomid subfamily <br />groupings may have merit in IBI <br />development. Faunal regions for benthic <br />macroinvertebrate taxa indicate an <br />elevational gradient in two groups of taxa. <br />They also represent, to some extent, <br />variation in their tolerance to environmental <br />degradation. Future analyses should <br />explore the utility of urging data for <br />benthic macromvertebrate taxa with data for <br />chironomid subfamilies. <br />The results for fish presence/absence data <br />indicate three fish faunal regions in the <br />upper Rio Grande drainage. These fish <br />faunal regions appear to have some degree <br />of drainage specificity that is caused by the <br />presence or absence of a few key species. <br />Site groupings with relative abundance data <br />for fish suggest two things. First, relative <br />abundance data may have utility. for <br />identifying acceptable versus unacceptable <br />sites with respect to criterion related to <br />desired abundance of certain species. <br />Second, relative abundance data may be <br />useful in identifying reference sites for use <br />with an IBI. <br />Several analyses would provide a clearer <br />understanding of how to proceed with <br />development of IBI's. Future analyses of <br />fish data should determine if fish faunal <br />regions identified on a coarser taxonomic <br />basic, e.g., trophic guilds and/or <br />reproductive guilds, are more consistent <br />with ecoregions obtained with <br />environmental data. Use of alternative <br />taxonomic schemes would accommodate <br />Regier's (1993) observation that "normal <br />and good" doesn't necessarily mean pristine <br />and undisturbed. Alternative taxonomic <br />schemes may also provide an effective <br />means to handle variation between drainages <br />that lie in the same aquatic ecoregion. <br />Similarly, future analyses should determine <br />if a coarser taxonomic classification for <br />chironomids would yield greater similarity <br />with faunal regions obtained with fish <br />species data. In northern New Mexico, our <br />a priori expectation was that there would be <br />a close parallel between -fish distribution and- <br />clvronomid distribution. A cold-water fish <br />fauna dominated by salmonids and selected <br />cypriniforms was expected to be <br />accompanied by a chironomid fauna <br />dominated by diamesine and orthocladine <br />species. However, the present analyses <br />have failed to demonstrate significant <br />similarity between fish and chironomid <br />faunal regions. The differences between <br />fish and chironomid faunal regions lie at <br />different landscape scales, i.e., the high <br />proportion of unique chironomid species per <br />site (about 25 %) confers a high degree of <br />specificity to individual reaches within a <br />stream for chironomid faunal regions. In <br />contrast, the presence of a few introduced <br />species confers some specificity to drainages <br />in fish faunal regions. <br />Similarity of Faunal Regions and <br />Aquatic Ecoregions <br />In general, classifications of sites by cluster <br />analysis on chironomid data have little <br />resemblance to the aquatic ecoregions <br />defined by analysis of environmental <br />variables. This could indicate that an IBI <br />based solely on chironomid species may not <br />be feasible for the upper Rio Grande. The <br />faunal regions obtained using fish <br />presence/absence data had some similarity <br />to the aquatic ecoregions. However, the <br />fish faunal regions also had some degree of <br />