An evaluation of the accuracy and precision of a stand-alone submersible continuous ruminal pH measurement system

The objectives of this study were 1) to develop and evaluate the accuracy and precision of a new stand-alone submersible continuous ruminal pH measurement system called the Lethbridge Research Centre ruminal pH measurement system (LRCpH; Experiment 1); 2) to establish the accuracy and precision of a well-documented, previously used continuous indwelling ruminal pH system (CIpH) to ensure that the new system ( LRCpH) was as accurate and precise as the previous system ( CIpH; Experiment 2); and 3) to determine the required frequency for pH electrode standardization by comparing baseline millivolt readings of pH electrodes in pH buffers 4 and 7 after 0, 24, 48, and 72 h of ruminal incubation ( Experiment 3). In Experiment 1, 6 pregnant Holstein heifers, 3 lactating, primiparous Holstein cows, and 2 Black Angus heifers were used. All experimental animals were fitted with permanent ruminal cannulas. In Experiment 2, the 3 cannulated, lactating, primiparous Holstein cows were used. In both experiments, ruminal pH was determined continuously using indwelling pH electrodes. Subsequently, mean pH values were then compared with ruminal pH values obtained using spot samples of ruminal fluid (MANpH) obtained at the same time. A correlation coefficient accounting for repeated measures was calculated and results were used to calculate the concordance correlation to examine the relationships between the LRCpH-derived values and MANpH, and the CIpH-derived values and MANpH. In Experiment 3, the 6 pregnant Holstein heifers were used along with 6 new submersible pH electrodes. In Experiments 1 and 2, the comparison of the LRCpH output (1- and 5-min averages) to MANpH had higher correlation coefficients after accounting for repeated measures (0.98 and 0.97 for 1- and 5-min averages, respectively) and concordance correlation coefficients (0.96 and 0.97 for 1- and 5-min averages, respectively) than the comparison of CIpH to MANpH (0.88 and 0.87, correlation coefficient and concordance correlation coefficient, respectively). The concordance correlation analysis indicated that the ruminal pH data for LRCpH ( 1- and 5-min averages) vs. MANpH had location shifts that were smaller than those of the CIpH vs. MANpH. However, the scale shift was similar between the LRCpH and the CIpH. The plotted data from both systems closely resembled the line y = x, indicating that both systems were accurate and precise. In Experiment 3, changes in baseline millivolt readings for pH readings after 24, 48, or 72 h of ruminal incubation were not significantly different than zero, indicating that daily standardization of new electrodes was not essential. Results from this study indicate that the LRCpH system can accurately and precisely measure ruminal pH; thus, it provides increased opportunity for researchers to measure ruminal pH and the occurrence of ruminal acidosis in unrestrained cattle.