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The concentration of strontium and other minerals in animal feed ingredients

Published online by Cambridge University Press:  04 February 2014

L.C. Browning*
Affiliation:
Faculty of Veterinary Science, The University of Sydney, Camden, NSW 2570, Australia
A.J. Cowieson
Affiliation:
Faculty of Veterinary Science, The University of Sydney, Camden, NSW 2570, Australia
*
Corresponding author: [email protected]

Summary

Variance in macro- and micro-mineral concentration in feed ingredients for farmed livestock contributes to sub-optimal performance and may compromise health and welfare. Although routine quality assurance and quality control procedures in feed mills or integrated poultry or swine businesses may track variance in the concentration of minerals of immediate nutritional importance, such as phosphorus (P), calcium (Ca) and sodium (Na), micro-minerals such as strontium (Sr) attract less attention. In order to create a framework for further study, the mineral concentration in more than 130 animal feed ingredients commonly used in Australia were analysed by inductively coupled plasma optical emission spectroscopy (ICP-OES). Due to a dearth of information, the principal focus of the survey was Sr, but the concentration of Ca, P, magnesium (Mg), manganese (Mn), potassium (K), iron (Fe), copper (Cu), zinc (Zn), sulphur (S) and Na were analysed concurrently. Generally the minerals present at the highest concentrations in the various feed ingredients examined were Ca, P and Mg. As anticipated, the ingredients with the highest concentrations of Ca and P were inorganic phosphates, limestone and meat and bone meal. The average Ca concentration in limestone was 393 g/kg but a range of 376–415 g/kg was observed which may be nutritionally important. Furthermore, the Mg concentration in limestone ranged from 7–535 mg/kg suggesting some contamination by dolomite lime sources. A total of 24 meat and bone meal samples were included in the analysis and mean Ca and P concentrations were 109 and 54 g/kg respectively. However, the range of Ca and P in meat and bone meal was considerable with Ca concentrations from 51–148 g/kg and P concentrations from 26–66 g/kg. A total of 81 cereal, grain legume and cereal by-product samples were included as part of the survey and these vegetable feed ingredients contained relatively low concentrations of most minerals with Ca, P, Mg and K dominating. The K concentration of soybean meal was found to be around 23 g/kg and ranged from approximately 22–27 g/kg. In comparison, the Sr concentration in the feed ingredients was low relative to other minerals, with limestone having the highest level of strontium at 329 mg/kg. Overall those feed ingredients from a mineral origin had the highest level of Sr. In addition, meat and bone meal had a relatively high concentration of Sr (around 159 mg/kg).

Type
Original Research
Copyright
Copyright © Cambridge University Press and Journal of Applied Animal Nutrition Ltd. 2014 

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References

Ammann, P., Shen, V., Robin, B., Mauras, Y., Bonjour, J. P. & Rizzoli, R. (2004) Strontium ranelate improves bone resistance by increasing bone mass and improving architecture in intact female rats. Journal of Bone and Mineral Research, 19, 20122020.CrossRefGoogle ScholarPubMed
Bowen, H.J.M. (1966) Trace Elements in Biochemistry. Academic Press London New York 241ppGoogle Scholar
Comar, C. & Wasserman, R. (1964) Strontium. Mineral metabolism, 2, 523572.Google Scholar
Davy, H. (1808) Electro-chemical researches on the decomposition of the earths; with observations on the metals obtained from the alkaline earths, and on the amalgam procured from ammonia. Philosophical Transactions of the Royal Society of London, 98, 333370.Google Scholar
Deeks, E.D. & Dhillon, S. (2010) Strontium Ranelate. Drugs, 70, 733759.Google Scholar
Gulhan, I., Bilgili, S., Gunaydin, R., Gulhan, S. & Posaci, C. (2008) The effect of strontium ranelate on serum insulin like growth factor-1 and leptin levels in osteoporotic post-menopausal women: a prospective study. Archives of gynecology and obstetrics, 278, 437441.Google Scholar
Leeson, S. & Summers, J.D. (2001) Scott's nutrition of the chicken, University Books Ontario.Google Scholar
Li, Z., Lu, W.W., Chiu, P.K., Lam, R.W., Xu, B., Cheung, K., Leong, J.C. & Luk, K.D. (2008) Strontium–calcium coadministration stimulates bone matrix osteogenic factor expression and new bone formation in a large animal model. Journal of Orthopaedic Research, 27, 758762.Google Scholar
Meunier, P., Slosman, D., Delmas, P., Sebert, J., Brandi, M., Albanese, C., Lorenc, R., Pors-Nielsen, S., De Vernejoul, M. & Roces, A. (2002) Strontium ranelate: dose-dependent effects in established postmenopausal vertebral osteoporosis—a 2-year randomized placebo controlled trial. Journal of Clinical Endocrinology & Metabolism, 87, 2060.Google Scholar
Meunier, P.J., Roux, C., Seeman, E., Ortolani, S., Badurski, J.E., Spector, T.D., Cannata, J., Balogh, A., Lemmel, E. M. & Pors-Nielsen, S. (2004) The effects of strontium ranelate on the risk of vertebral fracture in women with postmenopausal osteoporosis. New England Journal of Medicine, 350, 459468.Google Scholar
Mongin, P. (1980) Electrolytes in nutrition: a review of basic principles and practical application in poultry and swine. 3rd Annual International Mineral conference, Orlando, Florida, 1–15 .Google Scholar
NRC. (1994). Nutrient requirements of poultry, National Academies Press.Google Scholar
Pagano, A.R., Yasuda, K., Roneker, K. R., Crenshaw, T.D. & Lei, X.G. (2007) Supplemental Escherichia coli phytase and strontium enhance bone strength of young pigs fed a phosphorus-adequate diet. The Journal of nutrition, 137, 17951801.Google Scholar
Schroeder, H., Tipton, I.H. & Nason, A.P. (1972) Trace Metals In Man - Strontium And Barium. Journal of Chronic Diseases, 25, 491517.Google Scholar
Shahnazari, M., Lang, D., Fosmire, G., Sharkey, N., Mitchell, A. & Leach, R. (2007) Strontium administration in young chickens improves bone volume and architecture but does not enhance bone structural and material strength. Calcified Tissue International, 80, 160166.Google Scholar
Shahnazari, M., Sharkey, N.A., Fosmire, G.J. & Leach, R.M. (2006) Effects of strontium on bone strength, density, volume, and microarchitecture in laying hens. Journal of Bone and Mineral Research, 21, 16961703.Google Scholar
Skoryna, S.C. (1981) Effects of oral supplementation with stable strontium. Canadian Medical Association Journal, 125, 703712.Google Scholar
Smith, K. (1971) The comparative uptake and translocation by plants of calcium, strontium, barium and radium II. Triticum vulgare (wheat). Plant and soil, 34, 643651.Google Scholar
Stefansson, A., Gunnarsson, I. & Giroud, N. (2007) New methods for the direct determination of dissolved inorganic, organic and total carbon in natural waters by Reagent-Free™ Ion Chromatography and inductively coupled plasma atomic emission spectrometry. Analytica chimica acta, 582, 6974.Google Scholar
Wilkinson, S., Ruth, B. & Cowieson, A. (2013) Mineral composition of calcium sources used by the australian poultry feed industry. In: 24th annual australian poultry science symposium, 24, 4547.Google Scholar