全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Glomus intraradices Attenuates the Negative Effect of Low Pi Supply on Photosynthesis and Growth of Papaya Maradol Plants

DOI: 10.1155/2012/129591

Full-Text   Cite this paper   Add to My Lib

Abstract:

Low inorganic phosphorus (Pi) supply limits the photosynthetic process and hence plants growth and development. Contradictory reports exist in the literature on whether mycorrhyzal association can attenuate the negative effects of low Pi supply on photosynthesis and growth. In the present paper, the effect that low Pi supply may have on photosynthesis and growth of papaya Maradol plants was evaluated in intact plants and in those inoculated with two different strains of the arbuscular mycorrhizal fungi Glomus intraradices. Plant growth was significantly reduced as the Pi supply decreased. However, inoculation with any strain of G. intraradices was able to attenuate such effect. Without Pi in the nutrient solution, the mycorrhizal plants had on average 6.1 times and 7.5 higher photosynthesis than non mycorrhizal plants. The chlorophyll fluorescence values were significantly higher in mycorrhizal than in non-mycorrhizal plants. These results could be associated to an increased ability of mycorhyzal plants to take up Pi from the substrate, as they had higher Pi content than non-mycorrhizal plants. A high correlation was found between internal Pi content and plant biomass. The lower correlation between Pi content and photosynthesis, suggests that some photosynthates could had been used to maintain the symbiosis. 1. Introduction The scarcity of nutrients is a factor that limits physiological processes in plants, including photosynthesis, their growth, and development [1]. Phosphorus (P) deficiency normally reduces the root system development and plant establishment because it has an important role in cell division, growth, photosynthesis (Pn), respiration, energy storage, and transfer [2–4]. So that, in many agricultural systems, it is necessary to supply P in order to have good productivity [5]. When plants grow with nutrient scarcity, some of them are capable of modifying their root architecture, to exude organic acids, or to establish associations with some beneficial organisms as strategies to compensate for the low concentration of nutrient in the substrate. Among the beneficial organisms for plants, the arbuscular mycorrhizal (AM) fungi have a very important role in plant nutrition [6, 7]. It is through AM association that plants increase their capacity to take up organic phosphorus (Pi) from the soil solution [8–10] that normally translates into better growth than that of non-AM plants [11, 12]. Nevertheless, it has been reported that AM association could be more or less beneficial to the plant growth depending on the plant species and the AM fungi

References

[1]  B. S. Ripley, S. P. Redfern, and J. Dames, “Quantification of the photosynthetic performance of phosphorus-deficient Sorghum by means of chlorophyll-a fluorescence kinetics,” South African Journal of Science, vol. 100, no. 11-12, pp. 615–618, 2004.
[2]  J. Jacob and D. W. Lawlor, “Stomatal and mesophyll limitations of photosynthesis in phosphate deficient sunflower, maize and wheat plants,” Journal of Experimental Botany, vol. 42, no. 8, pp. 1003–1011, 1991.
[3]  H. Marschner, Mineral Nutrition of Higher Plants, Academic Press, San Diego, Calif, USA, 1995.
[4]  K. G. Raghothama, “Phosphate acquisition,” Annual Review of Plant Biology, vol. 50, pp. 665–693, 1999.
[5]  D. P. Schachtman, R. J. Reid, and S. M. Ayling, “Phosphorus uptake by plants: from soil to cell,” Plant Physiology, vol. 116, no. 2, pp. 447–453, 1998.
[6]  S. E. Smith and D. J. Read, “Uptake, translocation and transfer of nutrients in mycorrhizal symbioses,” in Mycorrhizal Symbiosis, S. E. Smith and J. D. Read, Eds., pp. 379–308, Academic Press, New York, NY, USA, 1990.
[7]  S. Ravnskov and I. Jakobsen, “Functional compatibility in arbuscular mycorrhizas measured as hyphal P transport to the plant,” New Phytologist, vol. 129, no. 4, pp. 611–618, 1995.
[8]  S. H. Burleigh, T. Cavagnaro, and I. Jakobsen, “Functional diversity of arbuscular mycorrhizas extends to the expression of plant genes involved in P nutrition,” Journal of Experimental Botany, vol. 53, no. 374, pp. 1593–1601, 2002.
[9]  G. Al-Karaki, B. McMichael, and J. Zak, “Field response of wheat to arbuscular mycorrhizal fungi and drought stress,” Mycorrhiza, vol. 14, no. 4, pp. 263–269, 2004.
[10]  P. E. Mortimer, E. Archer, and A. J. Valentine, “Mycorrhizal C costs and nutritional benefits in developing grapevines,” Mycorrhiza, vol. 15, no. 3, pp. 159–165, 2005.
[11]  A. Alarcón, F. T. Davies, J. N. Egilla, T. C. Fox, A. A. Estrada-Luna, and R. Ferrera-Cerrato, “Short term effects of Gloms claroideum and Azospirillum brasilense on growth and root acid phosphatase activity of Carica papaya L. under phosphorus stress,” Revista Latinoamericana de Microbiologia, vol. 44, no. 1, pp. 31–37, 2002.
[12]  G. Bohrer, V. Kagan-Zur, N. Roth-Bejerano, D. Ward, G. Beck, and E. Bonifacio, “Effects of different Kalahari-desert VA mycorrhizal communities on mineral acquisition and depletion from the soil by host plants,” Journal of Arid Environments, vol. 55, no. 2, pp. 193–208, 2003.
[13]  A. V. Trindade, J. O. Siquiera, and P. F. de Almeida, “Dependencia micorrízica de variedades comerciais de mamoeiro,” Pesquisa Agropecuária Brasileira, vol. 36, pp. 1485–1494, 2001.
[14]  C. A. Martin and J. C. Stutz, “Interactive effects of temperature and arbuscular mycorrhizal fungi on growth, P uptake and root respiration of Capsicum annuum L,” Mycorrhiza, vol. 14, no. 4, pp. 241–244, 2004.
[15]  S. E. Smith, F. A. Smith, and I. Jakobsen, “Functional diversity in arbuscular mycorrhizal (AM) symbioses: the contribution of the mycorrhizal P uptake pathway is not correlated with mycorrhizal responses in growth or total P uptake,” New Phytologist, vol. 162, no. 2, pp. 511–524, 2004.
[16]  D. R. Hoagland and H. I. Arnon, The Water-Culture Method for Growing Plants without Soil, vol. 347, California Experimental Agriculture Station Circular, Berkeley, Claif, USA, 1950.
[17]  T. Hoffmann, C. Kutter, and J. M. Santamaría, “Capacity of Salvinia minima baker to tolerate and accumulate As and Pb,” Engineering in Life Sciences, vol. 4, no. 1, pp. 61–65, 2004.
[18]  J. M. Phillips and D. S. Hayman, “Improved procedures for clearing roots and staining parasitic and vesicular-arbuscular mycorrhizal fungi for rapid assessment of infection,” Transactions of the British Mycological Society, vol. 55, pp. 158–161, 1970.
[19]  M. P. Sharma and A. Adholeya, “Effect of arbuscular mycorrhizal fungi and phosphorus fertilization on the post vitro growth and yield of micropropagated strawberry grown in a sandy loam soil,” Canadian Journal of Botany, vol. 82, no. 3, pp. 322–328, 2004.
[20]  T. S. L. Lau, E. Eno, G. Goldstein, C. Smith, and D. A. Christopher, “Ambient levels of UV-B in Hawaii combined with nutrient deficiency decrease photosynthesis in near-isogenic maize lines varying in leaf flavonoids: flavonoids decrease photoinhibition in plants exposed to UV-B,” Photosynthetica, vol. 44, no. 3, pp. 394–403, 2006.
[21]  I. M. Rao and N. Terry, “Leaf phosphate status, photosynthesis, and carbon partitioning in sugar beet. IV. Changes with time following increased supply of phosphate to low-phosphate plants,” Plant Physiology, vol. 107, no. 4, pp. 1313–1321, 1995.
[22]  E. Epstein and A. J. Bloom, Mineral Nutrition of Plants: Principles and Perspectives, Sinauer Associates, Sunderland, Mass, USA, 2004.
[23]  G. H. Krause and E. Weis, “Chlorophyll fluorescence and photosynthesis: the basics,” Annual Review of Plant Physiology and Plant Molecular Biology, vol. 42, no. 1, pp. 313–349, 1991.
[24]  D. P. Wright, J. D. Scholes, and D. J. Read, “Effects of VA mycorrhizal colonization on photosynthesis and biomass production of Trifolium repens L,” Plant, Cell and Environment, vol. 21, no. 2, pp. 209–216, 1998.
[25]  D. P. Wright, D. J. Read, and J. D. Scholes, “Mycorrhizal sink strength influences whole plant carbon balance of Trifolium repens L,” Plant, Cell and Environment, vol. 21, no. 9, pp. 881–891, 1998.
[26]  P. A. Olsson, I. M. Van Aarle, W. G. Allaway, A. E. Ashford, and H. Rouhier, “Phosphorus effects on metabolic processes in monoxenic arbuscular mycorrhiza cultures,” Plant Physiology, vol. 130, no. 3, pp. 1162–1171, 2002.
[27]  G. Cruz-Flores, S. Avilés Marín, and J. C. Cortés Castelán, “Estudio de adaptabilidad del triticale a diferentes dosis de calcio y fósforo en andisoles,” Terra, vol. 16, no. 1, pp. 63–69, 1998.
[28]  M. Gryndler, J. Larsen, H. Hrselová, V. Rezácová, H. Gryndlerová, and J. Kubát, “Organic and mineral fertilization, respectively, increase and decrease the development of external mycelium of arbuscular mycorrhizal fungi in a long-term field experiment,” Mycorrhiza, vol. 16, no. 3, pp. 159–166, 2006.
[29]  M. H. Ryan and J. F. Angus, “Arbuscular mycorrhizae in wheat and field pea crops on a low P soil: increased Zn-uptake but no increase in P-uptake or yield,” Plant and Soil, vol. 250, no. 2, pp. 225–239, 2003.
[30]  M. S. Schroeder and D. P. Janos, “Plant growth, phosphorus nutrition, and root morphological responses to arbuscular mycorrhizas, phosphorus fertilization, and intraspecific density,” Mycorrhiza, vol. 15, no. 3, pp. 203–216, 2005.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133