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opercula, and mandibles soon after administration. The <br />mark forms a band in the bony material, invisible in <br />normal light but which fluoresces yellow under <br />ultraviolet light. Three forms of TC have been used for <br />marking fish, including the pazent form, oxytetracycline <br />(OTC) and chlortetracycline. Oxytetracycline is <br />commonly used in the hatchery system because it does <br />not affect palatability of the diet, and mazk retention is <br />high (Weber and Ridgeway 1962, 1967; Weber and <br />Wahle 1969; Odense and Logan 1974; Koenings et al. <br />1968). <br />Tetracycline is typically administered in one of three <br />ways: ingestion of TC-dosed diet, intraperitoneal <br />injection, or immersion in a TC solution. In the dietary <br />method, the most widely used (Moring and Fay 1984), <br />efficiency increases as the calcium content of the feed is <br />reduced. Glucosamine, dimethyl sulfoxide, and <br />terephthalic acid (referred to as potentiators) can assist <br />in the uptake of TC from the diet and incorporation into <br />calcified structures (Weber and Ridgeway 1967; <br />Schidmore and Olsen 1969). <br />Contrary to the fmdings of Weber and Ridgeway <br />(1962,1967), Koenings et al. (1986) determined that the <br />length of the feeding period was secondary in <br />importance to marking fish at a size above which a lazge <br />percentage of the OTC assimilated was not <br />incorporated. Kcenings et al. (1986) suggested that <br />juvenile sockeye salmon (Oncorhynchus nerka) must be <br />larger than 40 mm (0.6 g) before orally administered <br />OTC produces a functional mazk. They also reported a <br />new fluorometric technique that detects OTC in the <br />skeletal structure before a visible ring is formed. This <br />new technique offers the additional advantage of being <br />able to distinguish the different forms of TC, increasing <br />its usefulness as a tagging agent. <br />The immersion process has not been as useful as <br />orally administered TC for tagging fish (Choate 1964; <br />Schidmore and Olson 1969; Hettler 1984); however, <br />encowaging results were reported recently when eggs <br />and larvae of ayu (Plecoglossus altivalis) were immersed <br />in TC solutions (200300 mg/L for 248 h for eggs and <br />200-300 mg/L for 3-24 h for larvae). Mark retention was <br />100% at 100 d post-immersion, with no special <br />preparations for detection (Tsukamoto 1985). <br />Injections of tetracycline have been used successfully <br />in marking killifishes (Bevelander and Goss 1962) and <br />flounders and cods (Jensen and Cummings 1967); <br />however, mazk incorporation may be slow with this <br />method (Moring and Fay 1984). <br />Moring and Fay (1984) listed the following <br />advantages and disadvantages. <br />Advantages <br />1. Marks aze essentially permanent (Jensen and <br />Cumming 1967; Weber and Ridgeway 1967; Weber and <br />Wahle 1969; Trojnaz 1973; Odense and Logan 1974). <br />2. Effect on survival and growth or behavior is limited <br />(Arnold 1966; Weber and Ridgeway 1967; Weber and <br />Wahle 1969; Schidmore and Olson 1969). <br />3. No handling or anesthetic is required, unless fish are <br />injected (Weber and Ridgeway 1967; Trojnar 1973; <br />Odense and Logan 1974). <br />4. Lazge quantities of fish can be tagged with relatively <br />little effort. <br />5. Coding and data processing aze simple. <br />6. Life stages and sizes from egg to smolt can be marked <br />(Trojnar 1973; Tsukamoto 1985). <br />7. Long-term storage of samples is possible (Trojnar <br />1973). <br />Disadvantages <br />1. Limited permutations for mazked groups (Weber <br />and Ridgeway 1967; Thomas 1975; Raymond 1974). <br />2. Wild fish are difficult to mark. <br />3. Lack of an external identifier, although external bony <br />parts (fms and opercles) fluoresce for a short period <br />(Choate 1964). <br />4. Fish must usually be sacrificed to enable detection. <br />5. Extraction and mark identification are tedious. <br />6. Sunlight deactivates TC fluorescence until <br />melanophores are developed (Choate 1964; Trojnar <br />1973; Odense and Logan 1974). <br />7. TC marks aze more readily detected in the fin rays of <br />small fish and the bones of larger fish (Trojnar 1973). <br />8. Hatchery stocks treated with TC for disease are <br />inadvertently tagged -which can be a source of <br />confusion in mazking studies. <br />Fluorescent Pigments <br />When fish are marked with fluorescent pigments, the <br />objective is to spray pigment granules onto or beneath the <br />skin (beneath the scales) and later detect their presence <br />under ultraviolet light. This method was first described in <br />1959, when it was used to mark landlocked Atlantic <br />salmon (Jackson 1959). Thereafter the technique was <br />used on a variety of species (Andrews 1979). <br />In the marking of smolt-sized salmon, pigment <br />granules aze sprayed through asand-blasting apparatus <br />at pressures of 7.0 to 8.4 kg/cm2, at a distance of 20 to <br />46 cm from the fish (Pribble 1976; Everhart and Youngs <br />1981; Evenson and Ewing 19$5). Fish aze typically dip- <br />netted onto an inclined, plastic-lined trough (Moring <br />and Fay 1984; Evenson and Ewing 1985) or conveyor <br />belt (Pribble 1976) on which they pass under the pres- <br />surized spray. Marking rates are high and have been <br />reported to be 32,000 sockeye salmon smolts per hour <br />by athree-person crew (Everhazt and Youngs 1981); or <br />25,000 juvenile Chinook or 40,000 juvenile rainbow trout <br />(Salmo gairdneri) on a conveyor system (Pribble 1976). <br />And recently, 35,000 spring Chinook salmon and sum- <br />mer steelhead were tagged per hour by afour-person <br />crew at the Cole River Hatchery on the Rogue River, <br />