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Last modified
7/14/2009 5:02:28 PM
Creation date
5/20/2009 11:00:45 AM
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UCREFRP
UCREFRP Catalog Number
7016
Author
Larval Fishes Laboratory.
Title
Development of Marking and Otolith-ageing Techniques for Colorado Squawfish
USFW Year
1986.
USFW - Doc Type
Report on Study-Phase 1.
Copyright Material
NO
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Y ? <br />!I -F= `'hi =e rr/1 m'. 4, 12 end h^'Irr' 3 5;7e <br />mg/l at 4, 12, an-di 36 hours; 500 mg/l at 4, 12, and <br />36 hours) with one control per life stage = 10 <br />lots per life stage. <br />--Three life stages will be tested (see Muth et al. <br />1985 for roundtail chub developmental data): (1) <br />embryo (pigmented eye stage; for roundtail chub, <br />ca 105 hours after fertilization), newly hatched <br />larvae (early protolarva; for roundtail chub, ca <br />126-156 hours after fertilization), and pre <br />swim-up larvae (late protolarva; for roundtail <br />chub, swim-up occurs ca 48 hours after hatching); <br />three life stages X 10 lots per life stage = 30 <br />lots. <br />--100-200 eggs/larvae per lot. <br />--Marking will be conducted in 1,000 ml beakers <br />containing the pH adjusted solutions; solutions <br />will be aerated and beakers placed in constant <br />temperature (19-20C) flow-through water baths; <br />larvae will not be fed during marking. <br />--After marking, 10 specimens from each lot will be <br />fixed and preserved; five in phosphate buffered <br />formalin (buffered near neutral; 10% buffered <br />formalin initial fixative, after 24 hr transferred <br />to 3% buffered formalin for preservation) and five <br />in 95% ethyl alcohol. The remaining eggs/larvae <br />will be transferred from the marking beakers to <br />three pairs of flow-through troughs (each pair <br />divided into 10 sections = 30 lots; eggs/larvae <br />will either be placed directly into troughs or <br />placed in containers, e,g., aerated jars). Samples <br />of 10 specimens from each lot will be taken every <br />seven days and fixed/preserved in the same manner <br />as noted above. Samples will be placed in separate <br />containers, labeled, and stored in the dark. <br />--Lots will be checked twice daily and dead fish- <br />removed, recorded, and preserved. <br />--Larvae (post swim-up) will be fed twice daily <br />(morning and evening) with brine shrimp nauplii <br />and commercial TetraMin Fry Diet and Staple Food. <br />--Water chemistry parameters (i.e., DO, pH, and <br />total water hardness) and water temperature will <br />be monitored during the experiment. <br />--Otoliths will be removed from specimens, mounted <br />on slides and examined under U-V light microscope <br />(Zeiss flourescent microsope, CSU Department of <br />Pathology, contact Charlie Curley). Precise <br />procedures will have to be worked out once <br />otoliths are removed from the specimens. It may <br />11
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