<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
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