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1 Department of Animal and Poultry Science, University of Guelph, Guelph, Ontario, Canada N1G 2W1
2 Animal Nutrition and Health Department, Animal Biology Division, Scottish Agricultural College, Kings Buildings, West Mains Road, Edinburgh, UK EH9 3JG
3 Department of Human Biology and Nutritional Sciences, University of Guelph, Guelph, Ontario, Canada N1G 2W1
4 Department of Population Medicine, University of Guelph, Guelph, Ontario, Canada N1G 2W1
Corresponding author: G. Cottee; e-mail: gcottee{at}uoguelph.ca.
| ABSTRACT |
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Key Words: dairy cow ruminal acidosis water choice
Abbreviation key: PR = preference ratio, SARA = subacute ruminal acidosis, SB = sodium bicarbonate
| INTRODUCTION |
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To meet the increasing demands for nutrients during early lactation, diets high in fermentable carbohydrates are fed to high producing dairy cows. These diets decrease ruminal pH because of increased concentrations of VFA and lactic acid (Underwood, 1992). Subacute ruminal acidosis (SARA) occurs when ruminal pH is depressed between a minimum pH of 5.2 and 5.6 (Cooper and Klopfenstein, 1996) and is characterized by decreased DMI, decreased milk production, diarrhea, and an increased incidence of laminitis (Nocek, 1997).
Sodium bicarbonate (SB) is an important buffer of ruminal pH (Erdman, 1988). Sodium bicarbonate enters the rumen through increased salivation during chewing and is routinely added to dairy cow rations to prevent a decrease in ruminal pH (Erdman, 1988; Kohn and Dunlap, 1998). Additionally, Cooper et al. (1996) found that sheep fed diets that depress pH chose pellets containing SB vs. pellets without.
Water has been used as a medium to deliver many supplements such as minerals for poultry (Shlosberg et al., 1998; Yoselewitz et al., 1990), sodium chloride for rats (Kraly et al., 1995; Rowland et al., 1995), and glucose for the transition dairy cows (Osborne et al., 2002). Sodium bicarbonate is commonly added to water as the key ingredient in drenches to increase blood-buffering capacity of race horses (Freestone et al., 1989; Lloyd and Rose, 1995). Several experiments have been conducted with dietary choice and ruminal acidosis in sheep (Cooper et al., 1996; Phy and Provenza, 1998a,b). The idea of supplementing water with SB and offering it as a choice to dairy cows subjected to SARA has not been previously reported. The hypothesis was that the lactating dairy cow subjected to SARA would select drinking water supplemented with SB to attenuate this condition. The effect of SARA on water intake was examined, and the dairy cows preference for SB-supplemented and unsupplemented water while subjected to SARA was determined.
| MATERIALS AND METHODS |
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Cows were allocated to an 8-wk experiment utilizing a repeated measures block design. The experiment was conducted from June through August 2001. Each week consisted of 5 supplementation (sampling) days (d 1 to 5) and 2 non-sampling days (d 6 to 7). Each of the 4 wk when SARA occurred was preceded by a non-SARA or control week.
Control diets were fed for ad libitum intake during wk 1, 3, 5, and 7. The SARA induction diets were fed on wk 2, 4, 6, and 8. A single TMR (Table 1
) was fed for ad libitum intake twice daily at 0700 and 1700 h during wk 1, 3, 5, and 7. During wk 2, 4, 6, and 8, 25% of the total TMR (DM basis) was replaced with 50:50 wheat:barley pellets to induce SARA as per the method developed by Keunen et al. (2002) (Figure 1
). During wk 2, 4, 6, and 8, TMR was restricted to a 2-kg DM basis at 0700 h. Two 0.5-h free choice TMR feeding intervals occurred between 1100 and 1130 h and between 1500 and 1530 h. Subacute ruminal acidosis was induced by providing wheat:barley pellets at 0900 h (2/3 of daily total or approximately 4 kg) and at 1300 h (remaining 1/3 of daily total or approximately 2 kg). The TMR was offered again for ad libitum intake at 1700 h.
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Water intake was measured continuously during this trial. Each stall was equipped with 2 Colorado stainless steel water bowls (Alfa Laval Agri. Inc., Peterborough, ON, Canada). A bowl was positioned 0.5 m above the ground on both the right and left side of the tie stall. Well water (see Table 2
for chemical analysis) was supplied to each water bowl. Supplementation of SB was provided via 2 in-line liquid injectors (Models DI 150 and DI 16-11GPM; Dosatron International, France) that injected a SB solution achieving a final concentration of 2.5 g/L. The flow rate to each bowl could be adjusted. The water bowls were connected to a C700 B-Pulse in-line water meter (ABB Water Meters Inc., Mississauga, ON, Canada). A pulse was generated 1x/L consumed and sent by switch closure through 18-ga. wire to a data logger (CR10X; Campbell Scientific, Edmonton, AB, Canada). Software collected data and recorded totals every 15 min, hourly and daily.
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Water samples were collected weekly from non-supplemented and SB-supplemented water sources. Water samples were analyzed at Agri-Food Laboratories (Guelph, ON, Canada). Water was analyzed for pH, total salts, total hardness, bicarbonates, minerals, sulfates, and phosphorus (AOAC, 1990); total solids (Gravimetric); chloride (ion-specific electrode); and nitrates (Technicon-Cadmium reduction/Spectrophotometric analysis). The ground water in this area is hard, containing high levels of calcium carbonate.
At the midpoint of the experiment, the 2 different types of water presented had their position switched, i.e., if the bicarbonate water was delivered originally in the left bowl it was altered to right bowl and vice versa for the unsupplemented water, which provided the opportunity to determine whether the animals could detect the presence of the 2 different types of water and determine whether the position had an effect on water preference.
Ruminal pH was monitored continuously during the trial using an adaptation of a technique developed by Dado and Allen (1993). A Sensorex Combi pH Electrode 450 CD (Sensorex, Stanton, CA) was placed through a rumen fistula into the anterior region of the rumen ventral sac. The pH data were collected every second and an average for each minute was calculated and stored for subsequent analysis (Keunen et al., 2002). For each 24-h period, ruminal pH was summarized into daily averages and calculated for time below pH 6, time below 5.6, area under pH 6, and area under pH 5.6.
The position of the pH electrodes were checked daily at 0930 h when manual ruminal samples were taken from the anterior region of the rumen ventral sac. Ruminal pH was measured using a Corning Benchtop pH meter (Model Corning 220; Corning Inc., Corning, NY) and an Accumet Gel-filtered Polymet Body Combination Electrode (Fisher Scientific, Fairlawn, NJ). Electrodes and pH transmitters were calibrated once weekly using buffer solutions (pH 4.0 and 7.0) (Fisher Scientific).
Milk production was recorded daily throughout the experiment. Milk samples were collected 2 times daily at 0500 and 1500 h. Morning and afternoon milk samples were pooled daily based on milk yields. Milk samples were analyzed for fat, protein, and lactose by infrared spectroscopy using the Foss System 400 (Foss Electric, Hillerød, Denmark) at Laboratory Services Division, University of Guelph (Guelph, ON, Canada).
DMI and Feed Analysis
A weekly composite TMR sample (Table 1
) and orts sample were collected for chemical analysis. Orts were weighed every day at 0900 h. Weights of TMR and wheat:barley pellets were recorded daily. Dry matter of feeds and orts were determined by drying in an oven at 60°C for 48 h (AOAC, 1990). The TMR and wheat:barley pellets were analyzed by Agri-Food Laboratory for determination of CP using the macro-Kjeldahl procedure (AOAC, 1990), ADF (AOAC, 1990; Undersander et al., 1993), NDF (Goering and Van Soest, 1970), and Ca, P, K, Mg, and Na (AOAC, 1990).
Statistical Design and Model
Analysis of variance was conducted using the SAS General Linear Models procedure with a repeated measures block design (SAS, 1998). For water intake, the model used was
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where
| Yijklm | = | dependent variable,
| ![]() | = | overall true mean,
| l | = | effect of animal (i = 1, 2, 3, 4),
| ßj | = | effect of bowl placement (j = 1, 2),
| ( ß)ij | = | effect of animal-bowl interaction,
| Tk | = | effect of day (k = 1, 2, 3, 4, 5),
| l | = | effect of time of day,
| (T )kl | = | effect of day-time of day interaction,
| m | = | effect of treatment, and
| ijklm | = | random residual error.
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For ruminal pH the model used was
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where
| Yijkl | = | observation on the treatment I in block ijkl,
| ![]() | = | overall true mean,
| l | = | effect of animal (i = 1, 2, 3, 4),
| Tj | = | effect of day (j = 1, 2, 3, 4, 5),
| k | = | effect of time of day,
| (T )ik | = | effect of day-time of day interaction,
| l | = | effect of treatment, and
| ijkl | = | random residual error.
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The data set was tested for normality requiring no transformations. Least square means are reported for comparison of pH and water parameters between control and SARA periods. Paired t-tests were completed for comparison between PR. A probability level of (P < 0.05) was considered significant.
| RESULTS AND DISCUSSION |
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Daily water intake is summarized in Table 4
. Mean daily water intake remained unaltered during the SARA periods (Table 4
). Intakes of both SB-supplemented water and unsupplemented water were also unaltered during the SARA periods (Table 4
). The average daily bicarbonate intakes from the SB-supplemented water for the SARA and control periods are summarized in Table 4
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Ruminal pH depression was at the most severe point for 3 h during the afternoon period following the second feeding of the wheat:barley pellets (Table 5
). During this period, the mean ruminal pH decreased (P < 0.0001) during SARA when compared with the control period. Ruminal pH increased following a large drinking bout during this afternoon period. During the SARA periods, the ruminal pH increased (P < 0.05) after a drinking bout from 5.67 ± 0.08 to 5.91 ± 0.08. During the control period, ruminal pH also increased (P < 0.05) after a drinking bout from 6.04 ± 0.04 to 6.19 ± 0.04. During the 3-h period of maximum pH depression, total water intake was higher (P < 0.0001) during the SARA period than during the control period. In addition, the intake of unsupplemented water increased (P = 0.005) during SARA when compared with the control period. The mean PR remained unchanged during the period of maximum ruminal pH depression (Table 5
).
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| CONCLUSIONS |
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| ACKNOWLEDGEMENTS |
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Received for publication May 14, 2003. Accepted for publication November 28, 2003.
| REFERENCES |
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