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<br />head, snout, eye, and fm lengths, as well as <br />snout-to-vent and snout-to-origin-of-fm (dor- <br />sal, anal and pelvic) lengths. <br /> <br />Snout-to-vent length is measured to the <br />posterior margin of the vent or anus. It is a <br />primary diagnostic character for many spe- <br />cies, especially at the family and sometimes <br />subfamily level. In the Upper Colorado <br />River System, most cyprinid larvae are readily <br />differentiated from catostomid larvae by <br />snout-to-vent lengths less than 72% SL. <br />Exceptions are most larvae of common carp <br />( Cyprinus carpio) and occasionally mesolarvae <br />of Colorado squawfISh. The term "preanal <br />length" is often applied to this measure but <br />might be misinterpreted as length to origin of <br />the anal fm. For many fishes, including <br />cypriniforms, the latter measure is approx- <br />imately the same as snout-to-vent length since <br />the anal fm begins at or near the posterior <br />margin of the vent. <br /> <br />Head length is typically measured to the <br />posterior margin of the operculum in juven- <br />iles and adults, but the operculum may be <br />absent or incomplete throughout much of the <br />larval period. Accordingly, many biologists <br />have redefmed head length for larvae to be <br />measured to the posterior end of the auditory <br />vesicle or the anterior or posterior margin of <br />the cleithrum, one of the first bones to ossify <br />in fish larvae (Berry and Richards 1973). <br />Unfortunately, the auditory vesicle and <br />cleithrum are not always easy to observe, <br />especially in postflexion mesolarvae and <br />metalarvae. Also, resultant measures to the <br />auditory vesicle are considerably anterior to <br />the eventual posterior margin of the oper- <br />culum. Snyder et al. (1977) and Snyder and <br />Douglas (1978) measured larval head length <br />to origin (anterior insertion) of the pectoral <br />fin. This measure has distinct advantages <br />over the alternatives -- the base of the <br />pectoral fm is readily observed throughout <br />the larval period (except in the few species <br />that hatch prior to pectoral bud formation), <br />it somewhat approximates the position of the <br />cleithrum (part of its supporting structure), <br />and it more nearly approximates the posterior <br />margin of the operculum than does the pos- <br />terior margin of the auditory vesicle. Accord- <br />ingly, we recommend this definition of head <br />length (Snyder 1983b) and have used it in all <br />our descriptive work. For purposes of consis- <br />tency, we apply it to juveniles as well as <br />larvae. The measure is most precisely deter- <br /> <br />mined while examining the specimen from <br />above or below and, if necessary, holding the <br />fm away from the body. <br /> <br />Body depths and widths are measured in <br />planes perpendicular to the horizontal axis of <br />the fISh. Many biologists report these as <br />maximum or minimum measures (e.g., great- <br />est head depth, greatest body depth, and least <br />caudal peduncle depth). However, for com- <br />parative purposes, it seems more logical to <br />specify standard reference points for such <br />measures as was done by Moser and Ahl- <br />strom (1970), Fuiman (1979), and Snyder and <br />Douglas (1978). Five specific locations, four <br />corresponding to specific length measure- <br />ments, are used herein: (1) immediately <br />posterior to eyes, (2) origin of pectoral fm, <br />(3) origin of dorsal fin, (4) immediately <br />posterior to vent, and (5) at anterior margin <br />of most posterior myomere (along the hori- <br />zontal myosepta). It is often desirable to <br />approximate position of reference points in <br />larvae prior to formation of the referenced <br />structure ( e.g., origin of dorsal fm in <br />protolarvae and flexion mesolarvae based on <br />position in later stages). Neither fms nor <br />fInfolds are included in depth measurements <br />herein. As mentioned earlier, care must be <br />used in evaluation of depth and width mea- <br />sures affected by body condition and gut <br />contents (e.g., measures at the origin of the <br />dorsal fm). <br /> <br />Other morphological characters such as <br />position, size, and form of the mouth and gut, <br />and related changes, can be among the more <br />useful characters for identification to the <br />species level. Size of the mouth, as well as its <br />position, its angle of inclination, and the form <br />of specific mouth structures are diagnostic for <br />some cypriniforms, especially in metalarvae. <br />Timing of mouth migration from terminal to <br />inferior position can be especially useful for <br />catostomid metalarvae. Gut loop length, tim- <br />ing of loop formation, and eventual degree <br />and form of the gut loops, folds, or coils can <br />be diagnostic for the larvae many fishes. <br />Such characters are especially useful in <br />distinguishing postflexion mesolarvae, meta- <br />larvae and early juveniles of certain catos- <br />tomids. <br /> <br />Pigmentation <br /> <br />Basic patterns of chromatophore distribu- <br />tion, and changes in these patterns as fish <br /> <br />13 <br />