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Dehydrogenase and phosphatase activities in soil as influenced by the growth of arid-land crops

Published online by Cambridge University Press:  27 March 2009

A. V. Rao ,
K. Bala  and
J. C. Tarafdar
A. V. Rao
Affiliation:
Division of Arable Cropping Systems, Central Arid Zone Research Institute, Jodhpur 342 003, India
K. Bala
Affiliation:
Division of Arable Cropping Systems, Central Arid Zone Research Institute, Jodhpur 342 003, India
J. C. Tarafdar
Affiliation:
Division of Arable Cropping Systems, Central Arid Zone Research Institute, Jodhpur 342 003, India
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Summary

The distribution of dehydrogenase activity (DHA) and the activities of phosphatases were studied in the rhizosphere of four varieties each of clusterbean (Cyamopsis tetragonoloba (L.) Taub.), mung bean (Vigna radiata (L.) Wilczek), moth bean (Vigna aconitifolia (Jacq.) Marechal) and pearl millet (Pennisetum americanum (L.) Leeke) grown in pots containing soil low in available P. Activities of dehydrogenase and phosphatases were greatest 25 days after sowing and remained constant from 50 days after sowing until crop maturity. Rhizosphere soils showed higher activities than other soils: 26–158% for acid phosphatase, 66–264% for alkaline phosphatase and up to 292% for DHA. Dehydrogenase and alkaline phosphatase activities were significantly higher in the rhizospheres of legumes than in those of P. americanum.In general, the rhizospheres of C. tetragonoloba ‘HFG314’, V. radiata ‘PDM62’, V. aconitifolia ‘IPCMO344’ and P. americanum ‘RCB2’ had higher activities than those of other varieties of the same species. Acid phosphatase activity was lower than alkaline phosphatase activity and differences between species and varieties were small and nonsignificant. The results suggest that the higher phosphatase activities in the rhizospheres of some crops may increase P availability and utilization from arid soils.

Type
Crops and Soils
Information
The Journal of Agricultural Science , Volume 115 , Issue 2 , October 1990 , pp. 221 - 225
Copyright
Copyright © Cambridge University Press 1990

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References

REFERENCES

Burn, R. G. (1982). Enzyme activity in soil: location and a possible role in microbial ecology. Soil Biology and Biochemistry 14, 423–427.CrossRefGoogle Scholar
Chhonkar, P. K. & Tarafdar, J. C. (1981). Characteristics and location of phosphatases in soil plant system. Journal of the Indian Society of Soil Science 29, 215–219.Google Scholar
Chhonkar, P. K. & Tarafdar, J. C. (1984). Accumulation of phosphatases in soils. Journal of the Indian Society of Soil Science 32, 266–272.Google Scholar
Cosgrove, D. J., Irving, G. C. & Bromfield, S. M. (1970). Inositol phosphate phosphatase of microbial origin. The isolation of soil bacteria having inositol phosphate phosphatase activity. Australian Journal of Biological Science 23, 339–343.CrossRefGoogle Scholar
Greaves, M. P. & Wabley, D. M. (1965). A study of the breakdown of organic phosphates by microorganisms from the root region of certain pasture grasses. Journal of Applied Bacteriology 28, 454–465.CrossRefGoogle ScholarPubMed
Hedley, M. J., White, R. E. & Nye, P. H. (1982). Plantinduced changes in the rhizosphere of rape (Brassica napus var. Emerald) seedlings. III. Changes in L value, soil phosphate fractions and phosphatase activity. New Phytologist 91, 45–56.CrossRefGoogle Scholar
Helal, H. M. & Sauerbeck, D. R. (1984). Influence of plant roots on C and P metabolism in soil. Plant and Soil 76, 175–182.CrossRefGoogle Scholar
Ingham, E. R. & Klein, D. A. (1984). Phosphatase activity of Penicillium citrinum submerged batch cultures and its relationship to fungal activity. Plant and Soil 81, 61–68.CrossRefGoogle Scholar
Kamath, M. S. & Oza, A. M. (1979). Crop characteristics in relation to use of fertiliser phosphorus. Bulletin of the Indian Society of Soil Science 12, 117–125.Google Scholar
Kitson, R. E. & Mellon, M. G. (1944). Colorimetric determination of phosphorus as molybdovanadophosphoric acid. Indian Engineering Chemical Analysis 16, 379–383.CrossRefGoogle Scholar
Kuprevich, V. F. & Shcherbakova, T. A. (1971). Comparative enzymatic activity in diverse types of soils. In Biochemistry (Eds. McLaren, A. D. & Skujins, J.), pp. 169–201. New York: Marcel Dekker.Google Scholar
Neal, J. L. (1973). Influence of selected grasses and forbs on soil phosphatase activity. Canadian Journal of Soil Science 53, 119–121.CrossRefGoogle Scholar
Sharpley, A. N. (1985). Phosphorus cycling in unfertilised and fertilised agricultural soils. Soil Science Society of America Journal 49, 905–911.CrossRefGoogle Scholar
Skujins, J. (1973). Dehydrogenase activity: an indicator of biological activity in arid soils. Bulletin of Ecological Research Communication 17, 235–241.Google Scholar
Stanton, W. R. (1966). Grain Legumes of Africa. Rome: FAO.Google Scholar
Tabatabai, M. A. (1982). Soil enzymes. In Methods of Soil analysis. Part 2. Chemical and Microbiological Properties, 2nd edn (Ed. Page, A. L.), pp. 903–947. Madison, Wisconsin: American Society of Agronomy.Google Scholar
Tabatabai, M. A. & Bremner, J. M. (1969). Use of p-nitrophenyl phosphate for assay of soil phosphatase activity. Soil Biology and Biochemistry 1, 301–307.CrossRefGoogle Scholar
Tarafdar, J. C., Bala, K. & Rao, A. V. (1989). Phosphatase activity and distribution of phosphorus in arid soil profiles under different land use patterns. Journal of Arid Environments 16, 29–34.CrossRefGoogle Scholar
Tarafdar, J. C. & Jungk, A. (1987). Phosphatase activity in the rhizosphere and its relation to the depletion of soil organic phosphorus. Biology and Fertility of Soils 3, 199–204.CrossRefGoogle Scholar