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Last modified
7/14/2009 5:02:36 PM
Creation date
5/20/2009 2:49:41 PM
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UCREFRP
UCREFRP Catalog Number
9550
Author
Snyder, D. E. and R. T. Muth.
Title
Catostomid Fish Larvae and Early Juveniles of the Upper Colorado River Basin - Morphological Descriptions, Comparisons, and Computer-interactive Key.
USFW Year
2004.
USFW - Doc Type
Fort Collins, CO.
Copyright Material
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<br />There is often a noticeable amount of intra- <br />as well as interregional variability in many of <br />the characters to be discussed. This variability <br />necessitates confirmation of identity based on as <br />many diagnostic characters as possible. <br /> <br />Myomeres <br /> <br />Myomeres, because they are obvious mor- <br />phological features and relatively consistent in <br />number and position, are one ofthe most useful <br />characters available for identification of larvae <br />above (and sometimes at) the species level, <br />especially for proto larvae and meso larvae. They <br />begin as part of the embryonic somites and are <br />usually formed in their full complement prior to <br />hatching. Throughout the proto larval and much <br />of the meso larval phase, myomeres are <br />chevron-shaped, but by the metalarval phase <br />they evolve to their typical three-angled adult <br />form. Fish (1932) and many subsequent authors <br />observed that there is a nearly direct, one-to-one <br />correlation between total myomeres and total <br />vertebrae (including Weberian ossicles in <br />cypriniforrns). Snyder (1979) and Conner et al. <br />(1980) summarized myomere and vertebral <br />counts for many cypriniform fishes. <br />The most anterior and most posterior myo- <br />meres are frequently difficult to distinguish. <br />The most anterior myomeres are apparent only <br />in the epaxial or dorsal half of the body; the first <br />is often deltoid in shape and is located immed- <br />iately behind the occiput. The most posterior <br />myomere is defined as lying anterior to the most <br />posterior complete myoseptum. Siefert (1969) <br />describes a "false (partial) myoseptum" posterior <br />to the last complete myoseptum which adds to <br />the difficulty of discerning the last myomere. <br />Early in the larval period, myomeres are most <br />readily observed using transmitted light. Polar- <br />izing filters, depending on thickness and certain <br />other qualities of the preserved tissues, can dra- <br />matically increase contrast between the muscle <br />tissue of myomeres and the myosepta that separ- <br />ate them. Myomeres of some metalarvae and <br />most juveniles are difficult to observe even with <br />polarizing filters; reflected light at a low angle <br />from one side and higher magnification some- <br />times facilitates observation. <br />Typical counts used in taxonomic work <br />include total, preanal, and postanal myomeres. <br />Partial counts are frequently used to also refer- <br />ence the location of structures other than the <br /> <br />vent or anus. The most generally accepted <br />method of making partial counts was described <br />by Siefert (1969) for distinguishing preanal and <br />postanal myomeres: "postanal myomeres in- <br />clude all [entire] myomeres posterior to an <br />imaginary vertical line drawn through the body <br />at the posterior end of the anus . . . Remaining <br />myomeres, including those bisected by the line, <br />are considered preanal." The technique is <br />equally applicable with other structures or points <br />of reference such as origins of fins or finfolds. <br />The opposite approach was used by Snyder et al. <br />(1977), Snyder and Douglas (1978), Loos and <br />Fuiman (1977) and, according to the latter <br />authors, Fish (1932 )-only entire myomeres were <br />included in counts anterior to points of <br />reference. Siefert's method is recommended as <br />standard procedure because resulting counts <br />more nearly approximate the number of vertebrae <br />to the referenced structures. <br />In the United States and Canada, the range <br />of total myomere (and vertebral) counts for <br />cyprinids, 28 to 52, is slightly larger and nearly <br />includes that for catostomids, 32 to 53. Ranges <br />for preanal and postanal myomere counts also <br />overlap with 19 to 35 and 9 to 22, respectively, <br />for cyprinids and 25 to 42 and 5 (possibly 3) to <br />14, respectively, for catostomids. Despite the <br />magnitude of overlap in these ranges, propor- <br />tions of postanal to preanal and preanal to total <br />myomeres will distinguish most cyprinids from <br />catostomids (Snyder 1979). The postanal to <br />preanal myomere proportion is at least 2/5 (often <br />greater than 1/2) for cyprinids (exclusive of <br />subfamily Cyprininae, the carps) and less (often <br />less than 1/3) for catostomids. Also, the pro- <br />portion of preanal to total myomeres is 5/7 or <br />less (often less than 2/3) for cyprinids and <br />greater (often greater than 3/4) for catostomids. <br />For cypriniform fishes in the Upper Colorado <br />River System the degree of overlap in total and <br />preanal myomere counts is less and larvae with <br />fewer than 42 total or 32 preanal myomeres can <br />be cyprinids only. <br /> <br />Fins and finfolds <br /> <br />Fin-ray meristics and fin pOSItIons are <br />among the most useful characters for later <br />meso larvae and metalarvae, especially among <br />the cyprinids. These data can be detennined <br />from older juveniles and adults or gleaned from <br />published descriptions of adults. The sequence <br /> <br />10 <br />
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