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Mineral Tolerance of Domestic Animals (1980)
Board on Agriculture (BOA)

Page
459
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459

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Strontium Strontium (Sr) is one of the alkaline earth metals, and, because of its high chemical activity, it never occurs free in nature (Pidgeon and Preisman, 1969~. It occurs in nature principally in the minerals stronti- anite (SrC03) and celestite (SrS041. The role of strontium in biological systems received little attention until the late 1940's, when it became obvious that 90SF is an abundant and potentially hazardous radioactive by-product of nuclear fission. ESSENTIALITY Strontium has been reported to act as a plant growth stimulant (Underwood, 1977) and to be capable of replacing the calcium required by Chiorella (Walker, 1953~. It has not, however, been shown to be essential for either plants or animals. A report by Rygh (1949) indicated that the omission of strontium from the mineral supplement fed to rats and guinea pigs consuming a purified diet resulted in growth depres- sion, an impairment of the calcification of the bones and teeth, and a higher incidence of dental caries. This work has not been confirmed. METABOLISM Early studies of the metabolism of strontium showed a close relation- ship with calcium (Fay et al., 19421. It was shown that strontium be- 459

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460 MINERAL TOLERANCE OF DOMESTIC ANIMALS havior in mammals was similar but not identical to that of calcium. The strontium ion (Sew) is very similar to the calcium ion (Ca+2), both chemically and physiologically, and it can substitute for calcium in physiological processes. These include muscular contraction, blood clotting, and bone formation. One difference which has been observed is that the rates of most of these processes are slowed when strontium is substituted for calcium. The major differences between strontium and calcium behavior were found relative to gastrointestinal absorp- tion, renal excretion, lactation, and placental transfer. It appears that whenever there is a metabolically controlled passage of ions across a membrane, calcium is transported more effectively than strontium (Comer and Wasserman, 19641. Once absorbed, the element has a strong affinity for the skeletal system. Strontium is poorly absorbed by adult animals on natural diets, with a large proportion of the ingested strontium appearing in the feces. SOURCES There is limited information on the normal intake of strontium by farm animals. With ruminants, this will be influenced by the strontium status of the soil and by the proportion of legumes to grasses in the herbage consumed. Mitchell (1957) found red clover growing on different soils ranged from 53 to 115 (mean 74) ppm strontium and ryegrass from 5 to 18 (mean 10) ppm strontium (dry basis). Strontium compounds are not added to animal diets and would occur in such diets as contaminants of other ingredients. TOXICOSIS Strontium (Sr+2) is less toxic than calcium (Ca+21. When strontium is fed along with low levels of calcium to young or growing animals, bone formation is disturbed and a condition known as "strontium rickets" develops (Bartley and Reber, 1961; Colvin and Creger, 1967; Colvin et al., 1972~. It has also been reported that strontium in the diet gives rise to insoluble phosphates during digestion and to a phosphorus de- ficiency (Jones, 1938~. The rachitogenic action of strontium is probably related to the levels and ratio of calcium and phosphorus in the diet. Knight et al. (1967) fed growing beef cattle diets containing two levels of calcium (0. 13 and 3.1 percent) and three levels of strontium (13, 200, and 2,000 ppm) for a 100-day period. High-calcium diets reduced weight gains and the digestibility of both dry matter and energy. The various

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Strontium 461 strontium levels had no effect on these criteria. The amount of stron- tium in bone ash increased with each added increment of strontium in the diet. The amount deposited was reduced by high-calcium additions. Bartley and Reber (1961) reported on the toxic effects of strontium in pigs (3 to 8 weeks old). Dietary treatments included 0.89 or 0.16 percent calcium and "zero" or 6,700 ppm strontium. The pigs fed 6,700 ppm strontium and 0.16 percent calcium were the most severely affected by incoordination and weakness, followed by posterior paralysis. Weber et al. (1968) fed dietary calcium levels of 0.72 and 1.0 percent with 3,000 and 6,000 ppm strontium as SrCO3 to chicks. Feeding 6,000 ppm strontium reduced growth rate more severely at the lower calcium level. Higher levels of strontium appeared to reduce calcium retention, while phosphorus utilization was apparently unaffected. Higher levels of strontium in bone ash were found at the lower calcium level. In a later study, Doberenz et al. (1969) fed high dietary levels of stable strontium to mature hens. Levels of 3,000 to 50,000 ppm of strontium as carbonate were fed for a 4-week period. The diet con- tained 2.9 percent calcium. The mature hen was able to tolerate con- siderable amounts of strontium in the diet. Egg weight, egg production, feed consumed, and body weights were unaffected by dietary levels up to 30,000 ppm. At a dietary level of 50,000 ppm strontium, egg weight, egg production, and feed consumed were significantly reduced. TISSUE LEVELS Gerlach and Muller (1934) found the strontium concentration of a wide variety of animal tissues ranged from 0.01 to 0.10 ppm, with no evi- dence of accumulation in any particular species, organ, or tissue. Stud- ies have demonstrated that as dietary levels of strontium are increased, the strontium absorbed is concentrated in the bones or skeletal system and not the soft tissue. In a study of the strontium content of cow's milk, Jury et al. ~ 1960) reported levels ranging from 31 to 65 ppm of the ash, or approximately 0.2 to 0.4 ppm of the whole milk. A report by Murphy et al. (1972) on samples of milk collected from cities in the United States gave results in close agreement with those of Jury e! a]. (1960~. MAXIMUM TOLERABLE LEVELS The effect of strontium is very dependent on the dietary level of cal- cium, with more pronounced effects observed at low-calcium levels. When dietary calcium levels are at NRC recommended levels for the

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462 MINERAL TOLERANCE OF DOMESTIC ANIMALS respective species, animals have a high tolerance for strontium. Mature animals can tolerate higher levels than the young. Assuming adequate calcium, dietary strontium levels as high as 2,000 ppm (0.2 percent) can be tolerated for extended periods of time, even by the young. Swine and poultry can tolerate 3,000 ppm (0.3 percent) and the laying hen can tolerate levels of 30,000 ppm (3 percent). Limited data indicate that animal diets normally contain about 200 ppm strontium. SUMMARY Strontium is one of the alkaline earth metals, and, because of its high chemical activity, it never occurs free in nature. It has not been shown to be essential for either plants or animals. Strontium is metabolized similarly to calcium by animals, and it can substitute for calcium in physiological processes. When strontium is fed with low levels of cal- cium to young or growing animals, bone formation is disturbed and a condition known as "strontium rickets" develops. Assuming adequate calcium, dietary strontium levels as high as 2,000 ppm (0.2 percent) can be tolerated for extended periods of time? even by the young. Swine and poultry can tolerate 3,000 ppm (0.3 percents, and the laying hen can tolerate levels of 30,000 ppm (3 percent).

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Strontium REFERENCES 465 Bartley, J. C., and E. F. Reber. 1961. Toxic effects of stable strontium in young pigs. J. Nutr. 75:21. Colvin, L. B., and C. R. Creger. 1967. Stable strontium and experimental bone anoma- lies. Fed. Proc. 26:416. Calvin, L. B., C. R. Creger, T. M. Ferguson, and H. R. Crookshank. 1972. Experimental epiphyseal cartilage anomalies by dietary strontium. Poult. Sci. S1:576. Comar, C. L., and R. H. Wasserman. 1964. Strontium, pp. 52~572. In C. L. Comar and F. Bronner, eds. Mineral Metabolism, vol. 2. Academic Press, New York. Doberenz, A. R., C. W. Weber, and B. L. Reid. 1969. Effect of high dietary strontium levels on bone and egg shell calcium and strontium. Calcif. Tissue Res. 4:180. Fay, M., M. A. Andersch, and V. G. Behrmann. 1942. The biochemistry of strontium. J. Biol. Chem. 144:383. Gerlach, W., and R. Muller. 1934. The occurrence of strontium and barium in human organs and excrete. Virchows Arch. Pathol. Anat. Physiol. 294:210. Jones, J. A. 1938. Metabolism of calcium and phosphorus as influenced by addition to the diet of salts of metals which form insoluble phosphates. Am. J. Physiol. 124:230. Jury, R. V., M. S. Webb, and R. J. Webb. 1960. The spectrochemical determination of total strontium in bone, milk and vegetation. Anal. Chem. Acta 22:145. Knight, W. M., V. R. Bohman, A. L. Lesperance, and C. Blincoe. 1967. Strontium retention in the bovine. J. Anim. Sci. 26:839. Mitchell, R. L. 1957. The trace element content of plants. Research (London) 10:357. Murthy, G. K., U. S. Rhea, and J. T. Peeler. 1972. Copper, iron, manganese, strontium, and zinc content of market milk. J. Dairy Sci. 55:1666. Pidgeon, L. M., and L. Preisman. 1969. Kirk-Othmer Encyclopedia of Chemical Tech- nology, vol. 19, 2nd ed. John Wiley & Sons, New York. Rygh, O. 1949. Research on trace elements. 1. Importance of strontium, barium and zinc. Bull. Soc. Chim. Biol. 31:1052. Underwood, E. J. 1977. Trace Elements in Human and Animal Nutrition, 4th ed. Aca- demic Press, New York. Walker, J. B. 1953. Inorganic micronutrient requirements of Chlorella. I. Requirements for calcium (or strontium), copper' and molybdenum. Arch. Biochem. Biophys. 46:1. Weber, C. W., A. R. Doberenz, R. W. G. Wyckoff, and B. L. Reid. 1968. Strontium metabolism in chicks. Poult. Sci. 47:1318.

Representative terms from entire chapter:

strontium strontium strontium