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<br />Keys -- Upper Colorado River Basin <br />Catostomids <br /> <br />The continual change in available char- <br />acte~s and c?aracter states and similarity of <br />specIes durmg larval and early juvenile <br />development are accommodated by separate <br />keys for eggs, each of four larval phases and <br />early juveniles up to 40 mm SL (about 50 mm <br />TL). Users must begin by determining the <br />devel?pmental interval of the specimen in <br />question: embryo (egg), protolarva, flexion <br />mesolarva, postflexion mesolarva metalarva <br />, , <br />or early (young-of-the-year) juvenile -- see <br />prec~ding section on developmental interval <br />termmology for complete defInitions. Users <br />must then determine standard length since <br />each key begins with size dependent charac- <br />ers. Alt.hough the polychotomous keys are <br />necessanly long and complex, often with <br />multiple paths leading to the same conclu- <br />ion, most specimens will require no more <br />than several steps to reach a terminus. <br />Supplemental keys based on selected skeletal <br />characters are provided to confIrm or better <br />resolve the identity of postflexion mesolarvae, <br />metalarvae and juveniles (specimens must be <br />cleared and preferably stained). <br /> <br />A discussion of characters useful in iden- <br />tifIcation of cypriniform larvae and diagrams <br />of anatomical features, methods of counts <br />and measures, gut loop phases, and selected <br />skelet~ structures (Figs. 2-6) precede results. <br />!he dIscussion of cypriniform characters <br />mclu?~s criteria for distinguishing the families <br />Cypnmdae and Catostomidae (see especially <br />fIns and fInfolds, last paragraph on myo- <br />meres, and .fIfth paragraph ?n morphology). <br />A comparative summary of diagnostic charac- <br />ters and species accounts immediately pre- <br />cede and follow this section, respectively. <br />The species accounts include full sets of <br />dorsal, lateral, and ventral view drawings. <br />Users of the keys should be familiar with this <br />material before proceeding. <br /> <br />The drawings in the species accounts are <br />fre9uently referenced in the keys, especially <br />t? illustrat.e specifIc patterns of melanophore <br />pIgmentation. However, referenced fIgures <br />are not necessarily of the species, develop- <br />men~al state, or size appropriate to the <br />portion of the key in which the reference is <br />made. Each spot of black or brown pigment <br />(melanin) represents a melanophore. In the <br /> <br />keys, melanophores refer only to those with <br />visible pigment (other melanophores may be <br />present but lack pigment or sufficient <br />amounts to be obvious under low power <br />magnification) . <br /> <br />These keys require the use of a low- <br />power microscope and some means of <br />m~asurin~ to ~he nearest 0.1 mm, e.g., <br />pomted dial calIpers, graduated mechanical <br />stage, or measuring eyepiece reticle with a <br />stage micrometer disc or slide for calibration. <br />If using the latter, be sure to set focus before <br />calibration; any subsequent changes in focus <br />or magnifIcation will require recalibration. If <br />using a zoom microscope and eyepiece reti- <br />cle, the scale can be calibrated for direct <br />millimeter measurement. A 10 mm reticle <br />scale in a lOX eyepiece focused on the speci- <br />men (or stage micrometer) with precisely 1X <br />of objective magnification will measure 10 <br />mm (note that zoom control magnifIcation <br />scales may not be accurate). At O.5X objec- <br />tive magnification, the reticle scale will <br />measure 20 mm (each 0.1 division then <br />equals 0.2 mm). If the specimen is not too <br />large, adjustment of magnifIcation to calibrate <br />the reticle scale to standard length (Fig. 4) of <br />the specimen will allow direct measurement <br />of specifIc structures or dimensions as a <br />percentage of standard length. <br /> <br />Except for fm lengths, measurements are <br />made parallel or perpendicular to the body <br />axis (Fig. 4). Specimens must be completely <br />s,ubmerged in fluid (usually water) and posi- <br />tioned such that their body axis is horizontal. <br />Flat pieces of glass can be used t.o prop or <br />hold-down a specimen. For fIsh which taper <br />from head to tail or have a pectoral fm pre- <br />venting it from lying flat on the bottom of a <br />dish, try suspending the head and part or <br />most of the body over the edge of a suffI- <br />ciently thick piece of glass. Lay another, <br />smaller and thinner piece of glass over the <br />tail to hold the specimen in position. Curved <br />or bent specimens that can't be straightened <br />or. gently. flattened under a cover slip or <br />thicker pIece of glass can be measured in <br />sections along the horizontal axis. Specimens <br />larger than the range of the measuring devise <br />also can be measured in sections. Measure- <br />ment units are the nearest whole or tenth of <br />a millimeter (e.g., a 12 mm specimen covers <br />the range 11.50 to 12.49 mm, and a measure <br />of 6.5 more precisely measures between 6.450 <br />and 6.549). <br /> <br />37 <br />