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...

Occurrence and Distribution of a Diatom-Diazotrophic Cyanobacteria Association during a Trichodesmium Bloom in the Southeastern Arabian Sea

DOI: 10.1155/2013/350594

Full-Text   Cite this paper   Add to My Lib

Abstract:

Symbiotic diatom-diazotrophic cyanobacteria association (DDA) of Rhizosolenia hebetata and Rhizosolenia formosa with endosymbiotic cyanobacteria Richelia intracellularis was noticed and documented for the first time during a bloom of the cyanobacterium Trichodesmium erythraeum in the oligotrophic shelf waters along Kochi and Mangalore transects, southeastern Arabian Sea (SEAS), during spring intermonsoon (April 2012). Although the host is frequently seen, the symbiont is rarely reported in the Indian EEZ. The presence of nitrogen-fixing symbiotic association of Rhizosolenia-Richelia along with Trichodesmium erythraeum highlights the significance of DDAs on the nutrient and energy budgets of phytoplankton in the oligotrophic environments of the Arabian Sea during spring intermonsoon. 1. Introduction Planktonic organisms that fix atmospheric nitrogen (diazotrophs) have a critical role in oceanic production and in the marine nitrogen cycle [1]. Abundance and growth rates of such organisms depend on their ability to assimilate various sources of nitrogen [2]. The availability of fixed nitrogen (such as nitrate and ammonium) can limit the productivity of the sea [3]. Diatom-diazotroph associations (DDAs) are widely reported in oligotrophic waters and have the capacity to form episodic, largely monospecific blooms that exhibit very high rates of carbon and nitrogen fixation worldwide [4–7]. Annually, Trichodesmium contributes 1–5?mmol?N?m?2?d?1; while diazotrophic diatoms, contribute 0.4–2.4?mmol?N?m?2?d?1, which forms one quarter of the total input of nitrogen to the sea [8]. Globally, DDAs fix 4.79?Tg?N?y?1 [9], which forms almost 25% of total input of nitrogen to the sea [8]. One of the most conspicuous free-living, diazotrophic species is the colony-forming cyanobacteria, a species of the Trichodesmium that is found throughout tropical and subtropical oceans and forms large-scale surface blooms [10]. A unique group of open ocean diazotrophs is the heterocystous cyanobacteria that live symbiotically with other members of phytoplankton, primarily diatoms. Such endosymbiotic associations help most of the diatoms to fix atmospheric nitrogen in oligotrophic waters with the help of such endosymbiotic associations [11–13]. The cyanobacteria, Richelia intracellularis and Calothrix rhizosoleniae, were found in association with diatom genera such as Rhizosolenia, Hemiaulus, Bacteriastrum,??and Chaetoceros. They are also seen as epiphyte or endosymbiont in Guinardia cylindrus in warm tropical and subtropical oligotrophic waters [6, 12, 14]. Only a few workers have

References

[1]  J. E. Dore, R. M. Letelier, M. J. Church, R. Lukas, and D. M. Karl, “Summer phytoplankton blooms in the oligotrophic North Pacific Subtropical Gyre: historical perspective and recent observations,” Progress in Oceanography, vol. 76, no. 1, pp. 2–38, 2008.
[2]  B. D. Jenkins, J. P. Zehr, A. Gibson, and L. Campbell, “Cyanobacterial assimilatory nitrate reductase gene diversity in coastal and oligotrophic marine environments,” Environmental Microbiology, vol. 8, no. 12, pp. 2083–2095, 2006.
[3]  A. White, “The trouble with the bubble,” Nature, vol. 488, pp. 290–291, 2012.
[4]  R. A. Foster, A. Subramaniam, C. Mahaffey, E. J. Carpenter, D. G. Capone, and J. P. Zehr, “Influence of the Amazon River plume on distributions of free-living and symbiotic cyanobacteria in the western tropical north Atlantic Ocean,” Limnology and Oceanography, vol. 52, no. 2, pp. 517–532, 2007.
[5]  L. Martínez, M. W. Silver, J. M. King, and A. L. Alldredge, “Nitrogen fixation by floating diatom mats: a source of new nitrogen to oligotrophic ocean waters,” Science, vol. 221, no. 4606, pp. 152–154, 1983.
[6]  A. L. Alldredge and M. W. Silver, “Abundance and production rates of floating diatom mats (Rhizosolenia castracanei and R. imbricata var. shrubsolei) in the Eastern Pacific Ocean,” Marine Biology, vol. 66, no. 1, pp. 83–88, 1982.
[7]  T. H. Mague, N. M. Weare, and O. Holm-Hansen, “Nitrogen fixation in the North Pacific Ocean,” Marine Biology, vol. 24, no. 2, pp. 109–119, 1974.
[8]  A. J. Poulton, M. C. Stinchcombe, and G. D. Quartly, “High numbers of Trichodesmium and diazotrophic diatoms in the southwest Indian Ocean,” Geophysical Research Letters, vol. 36, no. 15, Article ID L15610, 2009.
[9]  E. J. Carpenter, J. P. Montoya, J. Burns, M. R. Mulholland, A. Subramaniam, and D. G. Capone, “Extensive bloom of a N2-fixing diatom/cyanobacterial association in the tropical Atlantic Ocean,” Marine Ecology Progress Series, vol. 185, pp. 273–283, 1999.
[10]  D. G. Capone, J. A. Burns, J. P. Montoya et al., “Nitrogen fixation by Trichodesmium spp.: an important source of new nitrogen to the tropical and subtropical North Atlantic Ocean,” Global Biogeochemical Cycles, vol. 19, no. 2, Article ID GB2024, pp. 1–17, 2005.
[11]  R. A. Foster, A. Subramaniam, and J. P. Zehr, “Distribution and activity of diazotrophs in the Eastern Equatorial Atlantic,” Environmental Microbiology, vol. 11, no. 4, pp. 741–750, 2009.
[12]  M. E. Ferrario, V. Villafane, W. Helbling, and O. Holm-Hansen, “The occurrence of the symbiont Richelia in Rhizosolenia and Hemiaulus in the North Pacific,” Revista Brasileira de Biologia, vol. 55, no. 3, pp. 439–443, 1995.
[13]  T. A. Villareal, “Marine nitrogen-fixing diatom-cyanobacteria symbioses,” in Marine Pelagic Cyanobacteria: Trichodesmium and Other Diazotrophs, E. J. Carpenter, D. G. Capone, and J. G. Rueter, Eds., pp. 163–175, Kluwer Academic Publishers, Amsterdam, The Netherlands, 1992.
[14]  F. Gómez, K. Furuya, and S. Takeda, “Distribution of the cyanobacterium Richelia intracellularis as an epiphyte of the diatom Chaetoceros compressus in the western Pacific Ocean,” Journal of Plankton Research, vol. 27, no. 4, pp. 323–330, 2005.
[15]  M. O. P. Iyengar and T. V. Desikachary, “A systematic account of some marine Myxophyceae of the South Indian coast,” Journal of Madras University, vol. 16, pp. 37–63, 1944.
[16]  R. Subrahmanyan, “A systematic account of the marine plankton diatoms of the Madras coast,” Proceedings of the Indian Academy of Sciences B, vol. 24, no. 4, pp. 85–197, 1946.
[17]  V. V. Kulkarni, R. R. Chitari, D. D. Narale, J. S. Patil, and A. C. Anil, “Occurrence of cyanobacteria-diatom symbiosis in the Bay of Bengal: implications in biogeochemistry,” Current Science, vol. 99, no. 6, pp. 736–737, 2010.
[18]  K. B. Padmakumar, B. R. Smitha, L. C. Thomas et al., “Blooms of Trichodesmium erythraeum in the South Eastern Arabian Sea during the onset of 2009 summer monsoon,” Ocean Science Journal, vol. 45, no. 3, pp. 151–157, 2010.
[19]  K. Grasshoff, M. Erhardt, and K. Kremling, Eds., Methods of Seawater Analysis, Chemie, Weinheim, Germany, 2nd edition, 1983.
[20]  C. R. Tomas, Identifying Marine Phytoplankton, Academic press, New York, NY, USA, 1997.
[21]  R. Santhanam, N. Ramanathan, K. Venkataramanujam, and G. Jegatheesan, “Phytoplankton of the Indian seas,” in An Aspects of Marine Botany, Daya, Delhi, India, 1987.
[22]  T. J. Lyimo, “Distribution and abundance of the cyanobacterium Richelia intracellularis in the coastal waters of Tanzania,” Journal of Ecology and the Natural Environment, vol. 3, no. 3, pp. 85–94, 2011.
[23]  S. Janson, J. Wouters, B. Bergman, and E. J. Carpenter, “Host specificity in the Richelia-diatom symbiosis revealed by hetR gene sequence analysis,” Environmental microbiology, vol. 1, no. 5, pp. 431–438, 1999.
[24]  H. Habeebrehman, M. P. Prabhakaran, J. Jacob et al., “Variability in biological responses influenced by upwelling events in the Eastern Arabian Sea,” Journal of Marine Systems, vol. 74, no. 1-2, pp. 545–560, 2008.
[25]  A. N. Rai, E. S?derb?ck, and B. Bergman, “Cyanobacterium–plant symbioses,” New Phytologist, vol. 147, no. 3, pp. 449–481, 2000.
[26]  T. K. Westberry and D. A. Siegel, “Spatial and temporal distribution of Trichodesmium blooms in the world's oceans,” Global Biogeochemical Cycles, vol. 20, no. 4, Article ID GB4016, 2006.
[27]  N. Gandhi, A. Singh, S. Prakash et al., “First direct measurements of N2 fixation during a Trichodesmium bloom in the eastern Arabian Sea,” Global Biogeochemical Cycles, vol. 25, no. 4, Article ID GB4014, 2011.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133

WeChat 1538708413