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;. .:.:. ; <br />.., atch /Samp . ... <br />` ardne � s� <br />; <br />(rr gil: }; <br />:�1(kalinity- <br />:_tmgiu , <br />' .Gtlr)duCt'ivity. <br />: - <br />Ammonia � <br />.(mgiCNi' <br />� TRC2. <br />. mglLi <br />2691 (Performance <br />Control Water) <br />96 <br />66 <br />336 <br /><1.0 <br /><0.05 <br />2696 (Dilution Water <br />40 <br />23 <br />142 <br /><1.0 <br /><0.05 <br />3.2 Dilution /Control Water <br />The dilution water was reconstituted laboratory water prepared to match (t 15 %) the <br />hardness of the receiving water (38 mg /L as CaCO ENSR sample #10165). A <br />performance control was conducted concurrently using moderately hard reconstituted <br />water prepared according to USEPA (1994) guidelines. Initial characterization of the <br />dilution water and performance control water was as follows: <br />'As CaCO <br />'Total Residual Chlorine. <br />4.1 Test Method <br />4.0 TEST CONDITIONS <br />8503 - 099 - 193 -010 <br />The study was a static - renewal short -term chronic test using Ceriodaphnia dubia, and was <br />conducted based on USEPA (1994) and Colorado Department of Health (1 993) guidelines. <br />The biological responses measured were death (defined as no visible movement nor any <br />response to gentle prodding with a blunt probe) and young production. The complete test <br />protocol is included as Appendix B. <br />4.2 Test Duration <br />Test duration was 6 days, beginning 1445 July 29, 1997 and ending 1510 August 4, <br />1997. <br />4.3 Test Apparatus <br />Test chambers were 30 -m1 plastic beakers containing 15 ml of test solution. Ten replicate <br />chambers were tested for each treatment, with 1 organism per chamber (10 per <br />treatment). The test chambers were held in an environmental chamber under fluorescent <br />lighting with a photoperiod of 16 hours light: 8 hours dark; target test temperature was <br />2511 °C. <br />4.4 Feeding <br />Test organisms were fed 0.2 ml of a 1:1 mixture of algae (Selenastrum capricornutum) <br />suspension (3.0 X 10' - 3.5 X 10 cells /ml) and an incubated mixture of yeast, trout chow, <br />and cereal leaves (YTC; USEPA 1994) daily during testing. <br />5 <br />