Effects of Restricted Oxygen, Nitric oxide, and Mercuric Chloride on the Seed Germination and Early Elongation Growth of Rice

  • Yang Woon-Ho (National Institute of Crop Science, Rural Development Administration) ;
  • Kim Je-Kyu (International Technical Cooperation Center, Rural Development Administration) ;
  • Smucker Alvin J.M. (Department of Crop and Soil Sciences, Michigan State University)
  • Published : 2006.09.01

Abstract

Germination and early elongation of rice after germination were investigated in anoxic air treatment, nitric oxide gas treatment, and six concentrations of mercuric chloride solutions to determine the effects of limited oxygen environment, nitric oxide, and inhibited water flux through cell membrane in $17^{\circ}C$. Anoxic air treatment affected germination of tested six varieties very little. However root elongation rates were severely inhibited while shoot growth was affected less. Reductions in shoot and root elongations demonstrated genotypic variations. Nitric oxide delayed the germination of rice even though it didn't affect the final percent germination. Elongations of root and shoot were inhibited in nitric oxide treatment. The inhibitor effect of nitric oxide on the shoot elongation of rice was less severe, while nitric oxide completely inhibited the root emergence of rice. Concentrations of $HgCl_2$ greater than $300{\mu}M$ dramatically reduced the rate and percentage of germination when compared to distilled water treatment. The reduced percent germination showed the greatest variation among rice varieties in $500{\mu}M$ solution of mercuric chloride. Ansanbyeo, Jinheung, and Odaebyeo were affected less by $HgCl_2$, Nonganbyeo and Sangmibyeo were intermediate, and the germination of Andabyeo was greatly reduced by $HgCl_2$. Root elongation of germinated rice seedlings was more sensitive to oxygen deficits, nitric oxide, and $HgCl_2$ treatments than germination and shoot elongation. In conclusion, poor seedling establishment of rice sown in flooded paddy soils, in which the oxygen supply to the seeds is restricted, appears to the result of limited root elongation rate.

Keywords

References

  1. Bertani, A., I. Brambilla, S. Mapelli, and R. Reggiani. 1997. Elongation growth in the absence of oxygen: The rice coleoptile. Russian Journal of Plant Physiology 44 (4): 543-547
  2. Beligni, M. V. and L. Lamattina. 2000. Nitric oxide stimulates seed germination and de-etiolation, and inhibits hypocotyl elongation, three light-inducible responses in plants. Planta 210: 215-221 https://doi.org/10.1007/PL00008128
  3. Biswas, J. K. and M. Yamauchi. 1997. Mechanism of seedling establishment of direct-seeded rice under lowland conditions. Botanical Bulletin of Academia Sinica 38 (1): 29-32
  4. Daniels, M. J., T. E. Mirkov, and M. J. Chrispeels. 1994. The plasma membrane of Arabidopsis thaliana contains a mercury-insensitive aquaporin that is a homolog of the tonoplast water channel protein TIP. Plant Physiology 106: 1325-1333 https://doi.org/10.1104/pp.106.4.1325
  5. Francois, C., B. Francois, M. H. Eliet, and J. C. Maarten. 1998. Characterization of a maize tonoplast aquaporin expressed in zones of cell division and elongation. Plant Physiology 117: 1143-1152 https://doi.org/10.1104/pp.117.4.1143
  6. Guglielminetti, L., J. Yamaguchi, P. Perata, and A. Alpi. 1995. Amylolytic activities in cereal seeds under aerobic and anaerobic conditions. Plant Physiology 109 (3): 1069-1076 https://doi.org/10.1104/pp.109.3.1069
  7. Horton, R. F. 1991. The effect of ethylene and other regulators on coleoptile growth of rice under anoxia. Plant Science 79(1): 57-62 https://doi.org/10.1016/0168-9452(91)90069-K
  8. Hoshikawa, K. 1974. The growing rice plant. An anatomical monograph. pp. 1-310
  9. Ishimoto, N. 1982. Calper-the agent based on calcium peroxide: an improved method of water-seeded rice cultivation by use of rice seeds coated with Calper. Japan Plant Protection Association (41): 25-28
  10. Kubota, F., Y. Takada, W. Agata, and K. Ishimaru. 1994. Evaluation of the seed-germination vigor of rice varieties by sodium dithionate treatment. Journal of the Faculty of Agriculture. Kyushu Univ. 38(3-4): 183-192
  11. Lu, Z. and P. M. Neumann. 1999. Water stress inhibits hydraulic conductance and leaf growth in rice seedlings but not the transport of water via mercury-sensitive water channels in the root. Plant Physiology 120: 143-152 https://doi.org/10.1104/pp.120.1.143
  12. Maggio, A. and R. J. Joly. 1995. Effects of mercuric chloride on the hydraulic conductivity of tomato root systems-Evidence for a channel mediated water pathway. Plant Physiology 109 (1): 331-335 https://doi.org/10.1104/pp.109.1.331
  13. Maurel, C. 1997. Aquaporins and water permeability of plant membranes. Annu. Rev. Plant Mol. Biol. 48: 399-429 https://doi.org/10.1146/annurev.arplant.48.1.399
  14. Perata, P., N. Geshi, J. Yamaguchi, and T. Akazawa. 1993. Effects of anoxia on the induction of alpha-amylase in cereal seeds. Planta 191(3): 402-408
  15. Perata, P., L. Guglielminetti, and A. Alpi. 1997. Mobilization of endosperm reserves in cereal seeds under anoxia. Annals of Botany 79: 49-56 https://doi.org/10.1093/oxfordjournals.aob.a010306
  16. Wan, X. C. and J. J. Zwiazek. 1999. Mercuric chloride effects on root water transport in aspen seedling. Plant Physiology 121 (3): 939-946 https://doi.org/10.1104/pp.121.3.939
  17. Zhang, W. H. and S. D. Tyerman. 1999. Inhibition of water channels by $HgCl_2$ in intact wheat root cells. Plant Physiology 120: 849-857 https://doi.org/10.1104/pp.120.3.849