The effect of cation-anion difference on calcium requirement, feed intake, body weight gain, and blood gasses and mineral concentrations of dairy calves

Our objective was to examine the effects of two diets with different cation-anion differences on Ca requirements in the growing calf. Holstein calves (n = 48, 24 males) were blocked at 56 to 70 d after birth (80+/-10 kg of body weight) according to sex and birth date and assigned randomly in a 2 x 3 factorial arrangement of dietary treatments containing cation-anion differences as meq (Na + K) - (Cl + S)/kg of diet dry matter and Ca content of 1) 0 and 0.35%, 2) 0 and 0.50%, 3) 0 and 0.65%, 4) 200 and 0.35%, 5) 200 and 0.50%, and 6) 200 and 0.65%. Feed intake and average daily gain did not differ among treatment groups. Plasma pH and Ca were unaffected by dietary Ca content or dietary cation-anion difference. Plasma Cl and P decreased linearly with increasing Ca content in the diet. Plasma HCO3 increased linearly with increased dietary Ca content. Plasma HCO3 and partial pressure of CO2 were higher in calves fed the 200 compared with calves fed the 0 cation-anion difference diets. Plasma Cl was, however, lower in calves fed the 200 compared with calves fed the 0 meq diets. An interaction of Ca content and dietary cation-anion difference was detected for plasma P content. Urinary pH increased linearly with increasing dietary Ca content. Calves fed the 200 meq dietary cation-anion difference had higher urinary pH values than those fed the 0 meq diet. Urinary P excretion was not altered by dietary cation-anion difference or Ca content of the diet. Calves fed the 0 meq diet had higher urinary cocnentrations of Ca and Cl when compared with those fed the 200 meq diet. Bone ash, P, Ca, Mg, and K content of the 10th rib were not affected by dietary treatments. Breaking strength of the seventh and ninth ribs increased quadratically with increasing dietary Ca content. Dietary cation-anion difference had no effect on the breaking strength of the seventh and ninth ribs. Varying the dietary cation-anion difference from 0 to 200 meq/kg of dietary dry matter had no effect on Ca requirement of the growing calf.     

Interactions of dietary cation-anion balance and phosphorus: effects on growth and serum inorganic phosphorus in dairy calves

Thirty-six male and female Holstein and Jersey calves were assigned at weaning to a randomized complete block design in a 2 x 3 factorial arrangement to evaluate the influence of two dietary cation-anion balances (-14 and +39 meq(Na + K)-(Cl + S) per 100 g diet DM) and three amounts of dietary P (.22, .29, and .37%) on performance and P metabolism from 9 to 19 wk of age. Feed intake, average daily gain, and serum inorganic P were higher on the anionic diets and increased with increasing dietary P. Body weights were higher on the .37% P diets by wk 3 and on the anionic diets by wk 6. The interaction of dietary P and cation-anion balance was responsible for significant differences in calf performance; the anionic diet exhibited marked improvement over the cationic diet at the lowest P concentration. Results indicate that the availability of P for young dairy calves may be higher with anionic than cationic diets.     

Role of magnesium in the dietary cation-anion balance equation for ruminants

Eight midlactation Holstein cows (four primiparous) were assigned to replicated 4 x 4 Latin squares with a 2 x 2 factorial arrangement of treatments. The basal diet was formulated to contain 0 milliequivalents (Na + K) - Cl/100 g of diet DM. Treatment diets of high and low dietary cation-anion balance were achieved by adding appropriate amounts of supplemental Na + K (added on an equivalent basis) or Mg to the basal diet. Milk and protein yield were increased as well as DMI and FCM for Na + K diets The high concentration of cation increased milk fat percentage. The cation-anion balance (using Mg as a cation) had no effect on any of the production parameters observed. The higher cation-anion balances increased blood bicarbonate levels and plasma Na. Urinary Ca excretion was increased for the Mg diets. Urinary pH increased with both the source of cation (Na + K) and the concentration of cation (high) in the diet. other minerals were unaffected in milk, plasma, or urine. Responses measured in this trial reflect treatments calculated using the equation milliequivalents (Na + K) - Cl/100 g diet DM or (Na + K) - (Cl + S)/100 g diet DM, suggesting that Mg plays a minor role in dietary cation-anion balance.     

Influence of dietary cation-anion balance on milk, blood, urine, and rumen fluid in lactating dairy cattle

Twelve lactating Holstein cows were blocked according to age and milk production into groups of three cows and assigned to three 4 x 4 Latin squares in a split-plot design with subtreatments. Treatments on each square were four diets formulated to provide -10, 0, +10, or +20 meq/Na + K) -Cl/100 g diet DM. The four balances were achieved on squares 1, 2, and 3 by manipulating Na, K, and Cl, respectively. Actual milk yield was 8.6% higher on +20 than -10 averaged across the three squares. Blood pH and bicarbonate increased linearly with dietary cation-anion balance. Rumen pH increased linearly with dietary cation-anion balance, but fermentation patterns were largely unaffected. Urine pH increased linearly and quadratically with increasing dietary cation-anion balance. Square times balance response differences proved nonsignificant for all parameters except blood bicarbonate and rumen isovalerate, indicating responses could be attributed to the dietary cation-anion balance itself rather than to the effects of a single ion. Regulation of dietary cation-anion balance may become a useful tool for improving the performance of lactating dairy cattle.     

Influence of sodium chloride or potassium chloride on systemic acid-base status, milk yield, and mineral metabolism in lactating dairy cows

Our objective was to evaluate the response of lactating dairy cows to dietary Na, K, and Cl while holding cation-anion balance constant. Fifteen lactating Holstein cows, blocked according to age and previous milk yield, were assigned randomly to replicated 3 x 3 Latin squares with experimental periods of 3 wk. Diets contained sorghum silage and concentrate in a 40:60 ratio (DM basis) and were formulated to provide +32 meq of [(Na + K) - Cl]/100 g diet DM via one of three variations: 1) basal concentrations of dietary Na, K, and Cl, 2) basal diet with addition of 20 meq of Na and 20 meq of Cl/100 g in the form of 1.17% added NaCl, or 3) basal diet with the addition of 20 meq of K and 20 meq of Cl/100 g in the form of 1.56% added KCl. Free proton concentration in blood was increased by addition of NaCl and KCl; however, this increase did not appear to be physiologically significant, and no other measures of acid-base status were significantly affected. Plasma K was higher and plasma Mg was lower for the diets with supplemental NaCl or KCl than for basal diet. Urine mineral excretion reflected dietary mineral concentration, except Ca and Mg excretion rates were reduced by feeding the KCl diet. Milk yield reflected DM intake, which was lowest with supplemental NaCl. Results of this study indicate that, at a dietary cation-anion balance of +32 meq/100 g of diet DM, the balance of Na and K to Cl in the diet is a more important determinant of dietary impact on systemic acid-base status than actual dietary concentrations of Na, K, and Cl.     

Potassium requirement of dairy calves

Thirty-five Holstein and Jersey calves were blocked according to breed and sex, then randomly assigned at 4 wk of age to four dietary concentrations of K (.55, .84, 1.02, or 1.32% of DM) for a 10-wk period. Plasma K, Na, Ca, and Mg; body weight change; and feed intake were similar among the four treatments, as was average daily gain, which averaged .73 kg across all diets. In a second trial, 16 Holstein calves were blocked according to sex and randomly assigned at 6 wk of age to two concentrations of dietary K (.34 and .58% of DM) for an 8-wk period. Plasma Ca was higher at wk 8, and plasma Mg lower at wk 4, on the .58% K diet, while plasma Na and K were unaffected by dietary K concentration. Average daily gain for the .58% K group was .74 kg compared with .60 kg for calves receiving .34% K. In addition, both feed intake and body weight change were higher during the last 4 wk of the trial for the calves fed .58% K. As a result of the increased performance exhibited by the calves receiving .58% K, we conclude that the dietary K requirement of the growing dairy calf is within the range of .34 to .58%.     

Effects of various dietary cation-anion balances on response to experimentally induced hypocalcemia in sheep.

We examined the effect of dietary cation-anion balance on bone Ca mobilization, measured by challenging wethers with a 5.6% EDTA infusion at a rate of 1.4 ml kg of BW-1. Dietary cation-anion balance was calculated as milliequivalents [(Na + K) - (Cl + S)]. Six crossbred wethers (average BW, 67.8 kg) were fed rations with high Ca (.74% dry basis) or normal Ca (.45%) and three different dietary cation-anion treatments, which differed in their mineral supplementation. Dietary cation-anion balances were 354, 125, and 32 meq kg of DM-1 for control and two treatments. A 6 x 4 incomplete Latin square design (six treatments, four periods) was used with five 15-d periods of 14 d of adaptation followed by 1 d of EDTA infusion. Concentrations of total and EDTA titratable plasma Ca were not affected by the level of dietary Ca or treatments. The decrease in plasma EDTA titratable Ca at conclusion of EDTA infusion (120 min) was least in wethers fed the lowest cation-anion balance within high Ca, and recovery of plasma EDTA titratable Ca during the 240-min postinfusion period was faster for sheep fed this diet than for the control. The amount of Ca mobilized and its rate of mobilization during the EDTA infusion period tended to be higher for diets with reduced cation-anion balances than for the control. Thus, reducing cation-anion balance increased the sheep's ability to mobilize Ca during hypocalcemia.     

Effects of manipulating dietary cation-anion balance on macromineral balance in sheep.

Effect on macromineral balance in sheep of dietary excess of inorganic anions (Cl and S) or inorganic cations (Na and K) was studied. Dietary cation-anion balance was calculated as milliequivalents [(Na + K) - (Cl + S)] kg-1 of DM. Eight crossbred wethers were fed two levels of Ca, designated high Ca (.82%) or normal Ca (.48%), with four treatment each, three of which differed in dietary cation-anion balance. Control and two treatments had +284, +61, and -27 meq kg-1 of DM for high Ca and +343, +218, and +63 meq kg-1 of DM for normal Ca, respectively. A fourth treatment was control plus injection of vitamin D3 (16,670 IU kg-1 of BW). Reducing dietary cation-anion balance reduced Ca retention by increasing excretion of urinary Ca. Apparent absorption of Ca was similar across cation-anion balances. There was no correlation observed between dietary cation-anion balance and concentration of plasma Ca. No difference was observed in apparent absorption of Ca between high and normal Ca. This result may be related to an oversupply of dietary Ca. Magnesium retention as a proportion of that absorbed for lowest cation-anion balance was smaller than that for the intermediate balance and control plus vitamin D3, although not different from control. Results showed that reduced dietary cation-anion balance resulted in a reduction of Ca retention.     

Effects of copper sources and dietary cation-anion balance on copper availability and acid-base status in dairy calves.

Twenty-four Holstein and Jersey calves (14 Holstein), 4 to 11 d of age, were assigned randomly to six treatments in a 2 x 3 factorial arrangement to examine the effects of Cu sources and dietary cation-anion balance on Cu availability and acid-base balance. Treatments were cationic basal diet (20 meq of dietary cation-anion balance on a DM basis), cationic basal diet supplemented with CuO, cationic basal diet supplemented with CuSO4, anionic basal diet (-10 meq), anionic basal diet supplemented with CuO, and anionic basal diet supplemented with CuSO4. Copper sources did not show any effect on growth of calves. The cationic diet increased calf growth compared with the anionic diet at wk 12 of the experiment. Blood pH was increased by the cationic diet in comparison with the anionic diet at wk 8 and 12. Blood pH also was increased by CuSO4 compared with CuO treatment in the early period of the treatment. Blood bicarbonate concentration was decreased by CuO and the anionic diet. Interactions between Cu sources and cation-anion balance were found for blood pH and bicarbonate concentration. Liver Cu concentration was increased by CuSO4 but not by CuO supplementation compared with control. Therefore, CuSO4 was found to be highly available, whereas CuO was a very poorly available source of Cu for young calves.     

Parturient hypocalcemia in jersey cows fed alfalfa haylage-based diets with different cation to anion ratios

Jersey cows were fed three alfalfa haylage-based diets with different cation-anion balances beginning 6 wk preceding third or later calving and ending 24 to 36 h postpartum. Sodium and Cl as percentages of dietary DM were .08 and 1.66 in diet 1 (anionic, 5 cows), .44 and .91 in diet 2 (intermediate, 6 cows), and 1.60 and .34 in diet 3 (cationic, 6 cows). Cation-anion balances were 22, 60, and 126 meq/100 g DM; Ca:P ratios averaged 4:1. Cows fed diet 1 in comparison with cows fed diets 2 or 3 over 6 wk had similar concentrations of Ca, P, and Na but higher concentrations of Mg and K in plasma and higher urinary excretions of Ca and Mg. Concentrations of 1,25-dihydroxyvitamin D 3 d before parturition were higher in cows fed diet 1 than in cows fed diets 2 or 3. Within 36 h after calving, mean concentrations of Ca in plasma (mg/dl, range) of cows fed diets 1 to 3, respectively, were 7 (8.7 to 6.2), 6.5 (7.8 to 3.9), and 6.3 (7.8 to 3.8). Number of cases of clinical milk fever by diet were 0 of 5, 2 of 6, and 1 of 6 cows. Alteration of dietary cation-anion balance by addition of Cl may effectively reduce incidence and severity of parturient hypocalcemia.     

Lactational responses to dietary magnesium, potassium, and sodium during winter in Florida

Forty-eight midlactation Holstein cows were used to evaluate dietary treatments arranged as a 4 x 2 x 2 factorial: .26, .38, .48, or .60% Mg, .24 or .62% Na, and 1.14 or 1.59% K. Supplemental Mg, K, and Na were supplied by feed-grade magnesium phosphate, potassium bicarbonate, or sodium chloride. All dietary treatments were equal in Ca and P. There were no effects of dietary Na or K on feed intake or milk production. Feed intakes were equal with .26, .38, and .48% Mg but declined 4.9% with .60% Mg. Milk yields responded curvilinearly to dietary Mg. Similarly, 4% FCM yields responded curvilinearly, increasing 7% with .48% Mg compared with .26% Mg then declining with .60% Mg. Milk fat percentages were unaffected by dietary Mg concentration, but milk fat yields responded curvilinearly. Milk protein percentages declined linearly as dietary Mg increased. Plasma Mg concentrations increased linearly from 2.52 to 2.68 mg/dl as dietary Mg increased. Renal fractional excretions of Ca responded curvilinearly as dietary Mg increased and decreased as dietary K increased. Results of this experiment suggested that current recommendations for dietary Mg do not maximize lactational performance. A companion laboratory experiment showed that feed-grade magnesium phosphate had less alkalizing capacity than two MgO sources.     

Effects of reducing dietary cation-anion balance on calcium kinetics in sheep.

A Ca kinetic study with a four-compartment model being fitted to radioisotope and balance data using the CONSAM (conversational, simulation, analysis, and modeling) computer program was conducted to examine the effects of dietary cation-anion balance, calculated as milliequivalents [(Na + K] - (Cl + S)]. Twelve crossbred wethers were used as eucalcemic control (period 1); then Ca loss during lactation was simulated by continuous infusion of ethylene glycol tetraacetate (period 2). Dietary cation-anion balance was manipulated by supplementation of various mineral salts and was +339, +35, and -127 meq of kg DM-1 during period 1 and +429, +68, and -147 meq of kg DM-1 during period 2 for control and two treatments, respectively. Animals responded to the simulated lactational Ca loss (period 2) by increasing true intestinal absorption of Ca and bone resorption and by reducing Ca accretion by bone. No difference was observed in concentration of total Ca in plasma, but treatments produced increased concentration of plasma ionized Ca during both periods. Both treatments produced hypercalciuria during both periods, and the lowest cation-anion balance increased true intestinal absorption of Ca and reduced bone accretion during period 2. The size of total exchangeable Ca pool did not differ between treatments or periods, but amount of Ca movement between the pools increased with the intermediate cation-anion balance during period 1 and with both treatments during period 2 compared with control. These results indicated that feeding reduced cation-anion balance diets increased Ca flux through the exchangeable Ca pool with no changes in the size of the pool, particularly when Ca demand was increased.     

Short communication: Blood mineral and gas concentrations of calves born to cows fed prepartum diets differing in dietary cation-anion difference and calcium concentration

Eighty-two multiparous Holstein cows were fed diets differing in dietary cation-anion difference (DCAD) and Ca concentrations in a randomized block design experiment beginning 4 wk before anticipated calving to determine the effects on colostrum yield and quality and acid-base balance and mineral status of newborn calves. Treatments were arranged as a 2 × 2 factorial to provide 2 DCAD [?22 mEq/100 g of dry matter (NEG) or ?3 mEq/100 g of dry matter (NEU)] and 2 supplemental Ca concentrations (1.3 or 1.8% of dry matter). After calving, cows were milked within 2 to 8 h and colostrum yield was recorded. Calves were fed 200 g of IgG of a commercial colostrum replacer within 4 h of birth. No differences were observed in birth weight or dystocia score among treatments, which averaged 42.7 kg and 1.12, respectively. Colostrum yield was not different among treatments and averaged 8.75 kg. Colostrum quality, as measured using a Brix refractometer, was not affected by DCAD but was higher for 1.3% compared with 1.8% Ca: 21.58% and 19.87%, respectively. Colostrum IgG concentrations were higher for NEG compared with NEU and for 1.3% compared with 1.8% Ca. No differences were observed in concentrations of serum IgG, Ca, P, K, Cl, anion gap, or whole-blood pH, partial pressure of O₂, or SO₂ of calves among treatments. Serum Mg and lactate concentrations were higher and CO₂ tended to be lower for calves born to cows fed 1.3% compared with 1.8% Ca. Interactions of DCAD and Ca were observed for serum Na and Cl, which were higher for NEU-1.3% Ca and NEG-1.8% Ca compared with NEU-1.8% Ca and NEG-1.3% Ca. Whole-blood partial pressure of CO₂, and HCO₃ exhibited an interaction of DCAD and Ca and tended to be lower for NEU-1.3% Ca and NEG-1.8% Ca compared with NEU-1.8% Ca and NEG-1.3% Ca. Results of this trial indicate that feeding prepartum diets with 1.8% compared with 1.3% supplemental Ca reduced colostrum quality and serum concentrations of Mg and lactate in calves immediately after birth. Feeding NEG supported higher colostrum IgG concentrations. Blood mineral concentrations and blood gas balance tended to differ, but the effects were not consistent across DCAD and Ca.     

Dietary cation-anion balance and cation source effects on production and acid-base status of heat-stressed cows.

Two 4 x 4 replicated Latin square studies, each containing 8 lactating Holstein cows, were conducted simultaneously in south Georgia during the summer. The effects of dietary cation source (Na or K) and increasing dietary cation-anion balance (milliequivalents of Na + K - Cl per kilogram of feed DM) within cation source (control = 120.4 meq/kg of feed DM; Na source = 219.7, 347.8, 464.1 meq/kg of feed DM; K source = 231.2, 352.6, 456.0 meq/kg of feed DM) were determined on performance and acid-base chemistry during hot, humid weather. Cow body temperatures were elevated by environmental conditions but were not affected by dietary cation-anion balance. Differences in body temperature from dietary cation source probably were related to differences in cow BW. Intake of DM increased linearly, but yields of milk and FCM did not change with increasing dietary cation-anion balance, and cation source had no effect. Milk fat and protein percentages were not altered by dietary cation-anion balance, and greater milk fat and protein percentages from cows offered the Na versus K source diets probably were due to differences between cows in the two Latin squares. Alterations in blood acid-base chemistry with increasing dietary cation-anion balance were as expected. Greater blood buffering capacity, indicated by blood base excess and bicarbonate content, may be responsible for the improved feed intake.     

Effects of diet magnesium on acid-base status and calcium metabolism of dry cows fed acidogenic salts.

The objective was to study effects of dietary Mg on acid-base status and Ca metabolism of Holstein cows fed acidogenic diets with relatively high Ca concentrations. Eight nonlactating, nonpregnant Holstein cows were used in a switchback experiment with three 28-d periods. The normal Mg (.2%, dry basis) diet consisted of corn silage plus a concentrate mix supplemented with NH4Cl (126 g/d per cow) and (NH4)2SO4 (126 g/d per cow). The high Mg (.37%, dry basis) diet had MgSO4 substituted for an equivalent amount of S supplied by (NH4)2SO4 in the normal Mg diet. Cation-anion differences of the two diets were -302 (normal Mg) and -289 (high Mg) meq/kg of dietary DM. Compared with cows fed the normal Mg diet, those fed high Mg tended to have higher blood pH and plasma concentrations of total Ca but lower plasma concentrations of P and lower urinary excretion of ammonium and net acid. Cows fed the high Mg diet also tended to increase Mg excretion with a decrease in urinary excretion of Ca. Metabolic responses to intravenous infusion of Na2-EDTA were similar among cows fed either diet. Results indicate that increasing Mg intake of cows fed acidogenic salts was of no advantage with regard to Ca metabolism.     

Sulfur and chlorine play a non-acid base role in periparturient calcium homeostasis

The increased risk of periparturient hypocalcaemia through offering high-K feeds in the precalving period has been reported previously. Two experiments (experiment 1 and 2) investigated the effect of KCl fertilizer on pasture mineral concentration, the dietary cation-anion difference (DCAD), and the subsequent effect of this on periparturient plasma and urine mineral status. Experiment 2 examined the effect of precalving Mg source (MgO, MgSO4, and MgCl2) and postcalving Ca supplementation on the concentration of Ca and Mg in plasma and urine. Unexpectedly, pasture DCAD increased (P = 0.06) from 434 to 535 mEq/kg DM in experiment 1 as pasture K concentration decreased from 4.2 to 3.5%, primarily because of a corresponding and greater decrease in pasture Cl concentration (from 1.9 to 1.3%). Plasma Ca or Mg concentrations were not affected by pasture K concentration. A linear decline (P < 0.10) in urine Mg suggested a decline in Mg absorption as pasture K increased. In experiment 2, pasture DCAD decreased (P < 0.05) linearly from 403 to 350 mEq/kg DM as pasture K concentration decreased from 3.8 to 3.3%. However, precalving urine pH was not affected by the declining DCAD. Postcalving plasma Ca concentration was affected by precalving Mg source with MgSO4 > MgCl2 > MgO. Differences in acid-base balance do not explain the difference between Mg salts. These results indicate that precalving dietary S and Cl concentration plays an important role in Ca homeostasis, in addition to its role in acid-base balance. Supplementation with Ca postcalving increased plasma Ca concentration for 2 d postcalving. Milk production was not affected.     

Changing dietary electrolyte balance for dairy cows in cool and hot environments

Two Latin square studies, each containing eight primiparous cows (four Holstein, four Jersey), were conducted to determine the effect of changing dietary electrolyte balance during cool and hot environmental conditions on performance of lactating dairy cows. Electrolyte balance, expressed as Na + K - Cl in milliequivalents per kilogram of diet, was altered by changing K and Cl content in the diet using potassium bicarbonate or calcium chloride. Maximum and minimum temperatures averaged 26.7 and 15.0 degrees C during the cool phase and 32.3 and 22.5 degrees C during the hot phase of the study. Milk yield improved linearly with increasing electrolyte balance with nonsignificant treatment by phase interaction, whereas DMI of cows improved quadratically with increasing dietary electrolyte balance. A treatment by phase interaction for DMI was detected, although intake of DM reached a plateau at a similar dietary electrolyte balance during the cool and hot phases. Body (milk) temperature of cows appeared to be related to the level of feed consumed and varied by treatment within phase. Body (milk) temperature was higher during the hot phase of the experiment. Blood bicarbonate and pH were lowest in cows offered the low electrolyte balance (high Cl) diet, and blood and urinary Na + K-Cl increased linearly with increasing dietary electrolyte balance. The response to dietary electrolyte balance appeared to be mediated through blood buffering and the impact on physiologic systems of the cow.     

Influence of dietary sodium bicarbonate on the potassium metabolism of growing dairy calves.

We evaluated the influence of supplemental dietary NaHCO3 on K metabolism of young dairy calves. Thirty-two Holstein and Jersey male and female calves were blocked at 56 to 70 d after birth according to breed, sex, and age and assigned randomly to a 2 x 2 factorial arrangement of dietary treatments for 8 wk: .4% K with 0% NaHCO3, .4% K with 2% NaHCO3, .6% K with 0% NaHCO3, and .6% K with 2% NaHCO3. Feed intake was not affected by dietary KCl or NaHCO3 supplementation, but average daily gain increased with increased K and tended to be reduced by dietary NaHCO3. Plasma K was elevated by increased dietary K but generally was unaffected by NaHCO3. Urinary Ca excretion appeared to be reduced by NaHCO3; urine pH increased with supplemental NaHCO3. Results indicate 1) the K requirement of the growing calf is between .40 and .55% of diet DM, 2) because urinary K excretion was elevated by dietary NaHCO3, the K requirement may be increased when the diet is supplemented with NaHCO3, and 3) average daily gain and plasma K are sensitive indicators of dietary K in the growing calf.     

Effects of dietary calcium, vitamin D3, and corn supplementation on growth performance and mineral metabolism in young goats fed whole milk diets

Twenty-four male goats, approximately 2 to 4 wk of age, were allotted to four dietary treatments in a 2 X 2 factorial design and were fed a basal milk diet at 12.5% body weight for 20 wk. Vitamin D3 was added to the milk in two different amounts with and without supplemental CaCO3. At the end of wk 7, corn was added to all diets at 1% body weight. Over 20 wk, average daily gain was unaltered by addition of Ca or vitamin D3 to the diet. When corn was added to the diet, gains increased from 48 to 180 g/d. Plasma Ca concentrations were not affected by dietary treatment. Supplemental Ca decreased plasma Mg concentrations. Corn supplementation curtailed a depression in plasma Mg and seemed to prevent a whole milk-induced hypomagnesemia. Fecal excretion of all minerals measured was increased in goats fed supplemental Ca. Dietary Ca increased urinary Ca but decreased urinary Mg. Percentage of apparent absorption of Ca, Mg, and total ash was lower in Ca-supplemented goats, as was apparent retention of Ca and Mg. The physiological responses reported suggest the goat as a potential research model for mineral metabolism studies in other ruminants.     

Manipulating the dietary cation-anion difference via drenching to early-lactation dairy cows grazing pasture

Diets offered to grazing dairy cows can vary considerably in their dietary cation-anion difference (DCAD) and are often well in excess of what has been considered optimal. The effects of a range of DCAD on the health and production of pasture-based dairy cows in early lactation was examined in a randomized block design. Four groups of 8 cows were offered a generous allowance of pasture (45 +/- 6 kg/d of dry matter (DM) per cow) for 35 d and achieved mean pasture intakes of approximately 17 kg/d of DM per cow. Cows were drenched twice daily with varying combinations of mineral compounds to alter the DCAD. Dietary cation-anion difference ranged from +23 to +88 mEq/100 g of DM. A linear increase in blood pH and HCO(3)(-) concentration and blood base excess, and a curvilinear increase in the pH of urine with increasing DCAD indicated a nonrespiratory effect of DCAD on metabolic acid-base balance. Plasma concentrations of Mg, K, and Cl declined as DCAD increased, whereas Na concentration increased. Urinary excretion of Ca decreased linearly as DCAD increased, although the data suggest that the decline may be curvilinear. These results in conjunction with the increased concentrations of ionized Ca suggest that intestinal absorption of Ca or bone resorption, or both, increased as DCAD declined. Dry matter intake, as measured using indigestible markers, was not significantly affected by DCAD. However, the linear increase in the yield of linolenic acid, vaccenic acid, and cis-9, trans-11 conjugated linoleic acid in milk, as DCAD increased is consistent with a positive effect of DCAD on DM intake. Increasing DCAD did not significantly affect milk yield or milk protein, but the concentration and yield of milk fat linearly increased with increasing DCAD. The increased milk fat yield was predominantly a result of increased de novo synthesis in the mammary epithelial cells, although an increase in the yield of preformed fatty acids also occurred. Milk production results suggest that DCAD for optimal production on pasture diets may be higher than the +20 mEq/100 g of DM previously identified for total mixed rations.