Volume 64, no. 2, p. 784–788, 1998. p. 786, Table 1. Table 1 should read as shown below.
TABLE 1.
Inactivation rates of C. parvum oocysts exposed to measured concentrations of ammoniaa
| [NH3] (mol/liter) | K ± 95% CI/hb | Days to reach 99.999% inactivationc |
|---|---|---|
| 0.007 | 0.014 ± 0.004 | 34.3 |
| 0.026 | 0.027 ± 0.007 | 17.8 |
| 0.039 | 0.050 ± 0.005 | 9.6 |
| 0.060d | 0.047 ± 0.014 | 10.2 |
| 0.104 | 0.059 ± 0.034 | 8.1 |
| 0.148 | 0.066 ± 0.030 | 7.3 |
| 5.8e | 0.479 | 1 |
Based on data from the dye permeability assay after a 24-h exposure.
It was assumed that oocyst inactivation was a first-order process. The coefficient of inactivation was determined by regressing ln (P0/Pt) against time (derived from the equation Pt = P0 · e−Kt, where P0 is the initial percentage of viable oocysts, Pt is the percentage of viable oocysts at time t, in hours, and K is the coefficient of inactivation). The 95% confidence intervals (CI) were determined by multiplying the Student t value at the appropriate degree of freedom and at an α level (two-sided) of 0.025 by the standard deviations of K.
Calculated by the equation t = ln (P0/Pt)/K.
This concentration of NH3 and exposure time were used in the validation experiment shown in Table 2.
A power function, y = 2.523x−0.525 (r2 = 0.993), that fit the regression of [NH3] against days to reach 99.999% inactivation was used to determine the concentration of ammonia that would reduce the viability of oocysts by 99.999% in 1 day. The K value for this concentration of ammonia was then derived.
Page 787, column 2, line 9: “26.5 days” should read “55.1 days.”
