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Arbuscular mycorrhizae and phosphate solubilising bacteria of the rhizosphere of the mangrove ecosystem of Great Nicobar island, India

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Abstract

Mangroves form an important ecosystem of Great Nicobar, a continental island in the Bay of Bengal with luxuriant tropical rainforests. The rhizosphere of the mangrove plants of Great Nicobar was investigated for the presence of arbuscular mycorrhizal fungus (AMF) and phosphate solubilising bacteria (PSB). The soils of the Great Nicobar mangroves were silt–clays and were poor in phosphate content. Five species of AMF belonging to the genus Glomus were isolated. The %AMF colonization in the mangrove plants was between 0 and 17%, and the presence of AMF in the aerenchymatous cortex suggests that the mangrove plants may be aiding in AMF survival by providing oxygen. Two strains of phosphate solubilising Pseudomonas aeruginosa were found in the mangrove soils of Great Nicobar. Phosphate solubilisation by the two isolated strains was almost 70% under in vitro conditions. PSB may play a role in the mangrove ecosystems of Great Nicobar by mobilising insoluble phosphate. The plant roots could pick up the released phosphate directly or with the aid of AMF hyphae.

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References

  • Allen SE, Grimshaw HM, Parkinson JA, Quaramby C (1974) Chemical analysis of ecological materials. Blackwell, Oxford

    Google Scholar 

  • Andrade G (2004) Role of functional groups of microorganisms on the rhizosphere microcosm dynamics. In: Varma A, Abbot L, Werner D, Hampp R (eds) Plant surface microbiology. Springer, Berlin Heidelberg New York, pp 51–69

    Google Scholar 

  • Azcon-Aguilar C, Gianinazzi-Pearson V, Fardeau JC, Gianinazzi S (1986) Effect of vesicular arbuscular mycorrhizal fungi and phosphate solubilizing bacteria on growth and nutrition of soybean in a neutral-calcareous soil amended with 32P-45Ca-tricalcium phosphate. Plant Soil 96:3–15

    Article  CAS  Google Scholar 

  • Brady NC (1990) The nature and property of soils, 10th edn. Prentice Hall, New Delhi

    Google Scholar 

  • Brady NC, Weil RR (1999) The nature and properties of soils, 12th edn. Prentice Hall, New Jersey

    Google Scholar 

  • Brown AM, Bledsoe C (1996) Spatial and temporal dynamics of mycorrhizas in Jaumea carnosa, a tidal salt marsh halophyte. J Ecol 84:703–715

    Article  Google Scholar 

  • Cataldo DA, Harron M, Schrader LE, Youngs VL (1975) Rapid colorimetric determination of nitrate in plant tissues by nitration of salicylic acid. Commun Soil Sci Plant Anal 6:71–80

    Article  CAS  Google Scholar 

  • Chen PS Jr, Toribara TY, Warner H (1956) Microdetermination of phosphorous. Anal Chem 28:1756–1758

    Article  CAS  Google Scholar 

  • Cooke JC, Butler RH, Madole G (1993) Some observations on the vertical distribution of vesicular arbuscular mycorrhizae in roots of salt marsh grasses growing in saturated soils. Mycologia 85:547–550

    Article  Google Scholar 

  • Copley J (2000) Ecology goes underground. Nature 406:452–454

    Article  PubMed  CAS  Google Scholar 

  • Cui M, Caldwell MM (1996) Facilitation of plant phosphate acquisition by arbuscular mycorrhizae from enriched soil patches.II. Hyphae exploiting root-free soil. New Phytol 133:461–467

    Article  CAS  Google Scholar 

  • Garbaye J (1991) Biological interactions in the mycorrhizosphere. Experientia 47:370–375

    Article  Google Scholar 

  • Gerdemann JW, Nicholson TH (1963) Spores of mycorrhizal Endogone species extracted by wet sieving and decanting. Trans Br Mycol Soc 46:235–244

    Google Scholar 

  • Fitter AH, Garbaye J (1994) Interactions between mycorrhizal fungi and other soil organisms. Plant Soil 159:123–132

    Google Scholar 

  • Hackney CT, Padgett DE, Posey MH (2000) Fungal and bacterial contribution to the decomposition of Cladium and Typha leaves in nutrient enriched and nutrient poor areas of the Everglades, with a note on ergosterol concentrations in Everglades soils. Mycol Res 104:666–670

    Article  Google Scholar 

  • Hirrel MC, Gerdemann JW (1980) Improved growth of onion and bell pepper in saline soils by vesicular arbuscular mycorrhizal fungi. Soil Sci Soc Am J 44:654–655

    Article  CAS  Google Scholar 

  • Jackson ML (1973) Soil chemical analysis. Prentice Hall, New Delhi

    Google Scholar 

  • Koch MS, Snedaker SC (1997) Factors influencing Rhizophora mangle L. seedling development in Everglades carbonate soils. Aquat Bot 59:87–98

    Article  Google Scholar 

  • Kothamasi DM (2000) Arbuscular mycorrhizal diversity and plant community patterns in the insular tropical rainforest ecosystems of Great Nicobar Biosphere Reserve. PhD Thesis, University of Delhi

  • LeTacon F, Skinner FA, Mosse B (1983) Spore germination and hyphal growth of a vesicular–arbuscular mycorrhizal fungus, Glomus mosseae (Gerdemann and Trappe), under decreased oxygen and increased carbon dioxide concentrations. Can J Microbiol 29:1280–1285

    Article  CAS  Google Scholar 

  • Lugo AE, Snedaker SC (1974) The ecology of mangroves. Ann Rev Ecolog Syst 5:39–64

    Article  Google Scholar 

  • Nicolson TH (1955) The mycotrophic habit in grass. Thesis, University of Nottingham

  • Ong JE, Khoon GW, Clough BF (1995) Structure and productivity of a 20-year old stand of Rhizophora apiculata Bl. Mangrove forest. J Biogeogr 22:417–424

    Article  Google Scholar 

  • Pfeiffer CJ, Bloss HE (1988) Growth and nutrition of guayule (Parthenium argentums) in a saline soil as influenced by vesicular arbuscular mycorrhiza and phosphorous fertilization. New Phytol 91:211–220

    Google Scholar 

  • Phillips JM, Hayman DS (1970) Improved procedures for clearing roots and staining parasitic and vesicular arbuscular mycorrhizal fungi for rapid assessment of infection. Trans Br Mycol Soc 55:158–161

    Article  Google Scholar 

  • Pond EC, Menje JA, Jarell WM (1984) Improved growth of tomato in salinized soils by vesicular arbuscular mycorrhizal fungi collected from saline soils. Mycologia 76:74–84

    Article  Google Scholar 

  • Read DJ (1990) Mycorrhizas in ecosystems—natures response to the law of minimum. In: Hawksworth DL (ed) Frontiers in Mycology. 4th International Mycological Congress, Regensburg, CAB International. Wallingford, UK, pp 101–130

    Google Scholar 

  • Richards PW (1996) The tropical rain forest: an ecological study, 2nd edn. Cambridge University Press, Cambridge, UK

    Google Scholar 

  • Schenck NC, Pérez Y (1990) Manual for identification of VA mycorrhizal fungi. INVAM, 2nd edn. Synergistic Publications, Gainsville, FL

    Google Scholar 

  • Scholander PF (1968) How mangroves desalinate sea water. Physiol Plant 21:251–261

    Article  CAS  Google Scholar 

  • Sengupta A, Chaudhuri S (1990) Vesicular arbuscular mycorrhiza (VAM) in pioneer salt marsh plants of the Ganges river delta in West Bengal (India). Plant Soil 122:111–113

    Google Scholar 

  • Sengupta A, Chaudhuri S (2002) Arbuscular mycorrhizal relations of mangrove plant community at the Ganges river estuary in India. Mycorrhiza 12:169–174

    Article  PubMed  Google Scholar 

  • Smith SE, Read DJ (1997) Mycorrhizal symbiosis, 2nd Edn. Academic, London

    Google Scholar 

  • Subba Rao NS (1988) Biofertilizers in agriculture. Oxford and IBH Publishing, New Delhi

    Google Scholar 

  • Toro M, Azcón R, Barea JM (1998) The use of isotopic dilution techniques to evaluate the interactive effects of Rhizobium genotype, mycorrhizal fungi, phosphate solubilizing rhizobacteria and rock phosphate on nitrogen and phosphorous acquisition by Medicago sativa. New Phytol 138:265–273

    Article  CAS  Google Scholar 

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Acknowledgements

The authors thank Prof. C. Manoharachary, Osmania University, Hyderabad, and Prof. D.J. Bagyaraj, University of Agricultural Sciences, GKVK campus, Bangalore, for help in identification of the AMF species and structures; the anonymous referee and the editor for critical advice; Drs. R.S. Sharma and R. Tandon for help; Dr. V. Shimpale for assistance in the collection of the roots; the Forest Department of Andaman and Nicobar and the Botanical Survey of India, Port Blair Circle, for help and assistance; the Ministry of Environment and Forests, Government of India, for sanction of Project No. J22016/11/93–BR and CSIR for grant of Senior Research Fellowship to David Kothamasi.

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Kothamasi, D., Kothamasi, S., Bhattacharyya, A. et al. Arbuscular mycorrhizae and phosphate solubilising bacteria of the rhizosphere of the mangrove ecosystem of Great Nicobar island, India. Biol Fertil Soils 42, 358–361 (2006). https://doi.org/10.1007/s00374-005-0035-8

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