Hostname: page-component-8448b6f56d-jr42d Total loading time: 0 Render date: 2024-04-25T01:39:36.042Z Has data issue: false hasContentIssue false

Alleviation of solar ultraviolet radiation (UVR)-induced photoinhibition in diatom Chaetoceros curvisetus by ocean acidification

Published online by Cambridge University Press:  22 October 2014

Heng Chen
Affiliation:
Department of Marine Science, School of Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China
Wanchun Guan*
Affiliation:
Department of Marine Science, School of Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang 325035, China
Guoquan Zeng
Affiliation:
Zhejiang Mariculture Research Institute, Wenzhou 325005, China
Ping Li
Affiliation:
Marine Biology Institute, Shantou University, Shantou, Guangdong 515063, China
Shaobo Chen
Affiliation:
Zhejiang Mariculture Research Institute, Wenzhou 325005, China
*
Correspondence should be addressed to:G. Wanchun, Department of Marine Science, School of Life Sciences, Wenzhou Medical University, Wenzhou, Zhejiang, 325035, China. email: gwc@wmu.edu.cn

Abstract

The study aimed to unravel the interaction between ocean acidification and solar ultraviolet radiation (UVR) in Chaetoceros curvisetus. Chaetoceros curvisetus cells were acclimated to high CO2 (HC, 1000 ppmv) and low CO2 concentration (control, LC, 380 ppmv) for 14 days. Cell density, specific growth rate and chlorophyll were measured. The acclimated cells were then exposed to PAB (photosynthetically active radiation (PAR) + UV-A + UV-B), PA (PAR + UV-A) or P (PAR) for 60 min. Photochemical efficiency (ΦPSII), relative electron transport rate (rETR) and the recovery of ΦPSII were determined. HC induced higher cell density and specific growth rate compared with LC. However, no difference was found in chlorophyll between HC and LC. Moreover, ΦPSII and rETRs were higher under HC than LC in response to solar UVR. P exposure led to faster recovery of ΦPSII, both under HC and LC, than PA and PAB exposure. It appeared that harmful effects of UVR on C. curvisetus could be counteracted by ocean acidification simulated by high CO2 when the effect of climate change is not beyond the tolerance of cells.

Type
Research Article
Copyright
Copyright © Marine Biological Association of the United Kingdom 2014 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Andersson, A.J., Mackenzie, F.T. and Gattuso, J.-P. (2011) Effects of ocean acidification on benthic processes, organisms, and ecosystems. Ocean Acidification 8, 122153.Google Scholar
Badger, M.R., Andrews, T.J., Whitney, S., Ludwig, M., Yellowlees, D.C., Leggat, W. and Price, G.D. (1998) The diversity and coevolution of Rubisco, plastids, pyrenoids, and chloroplast-based CO2-concentrating mechanisms in algae. Canadian Journal of Botany 76, 10521071.Google Scholar
Beardall, J. and Raven, J.A. (2004) The potential effects of global climate change on microalgal photosynthesis, growth and ecology. Phycologia 43, 2640.Google Scholar
Beardall, J., Sobrino, C. and Stojkovic, S. (2009) Interactions between the impacts of ultraviolet radiation, elevated CO2, and nutrient limitation on marine primary producers. Photochemical and Photobiological Sciences 8, 12571265.CrossRefGoogle ScholarPubMed
Behrenfeld, M.J., Lean, D.R. and Lee, H. (1995) Ultraviolet-b radiation effects on inorganic nitrogen uptake by natural assemblages of oceanic plankton. Journal of Phycology 31, 2536.Google Scholar
Boelen, P., de Boer, M.K., Kraay, G.W., Veldhuis, M.J. and Buma, A.G. (2000) UVBR-induced DNA damage in natural marine picoplankton assemblages in the tropical Atlantic Ocean. Marine Ecology Progress Series 193, 19.Google Scholar
Caldeira, K. and Wickett, M.E. (2003) Oceanography: anthropogenic carbon and ocean pH. Nature 425, 365.CrossRefGoogle ScholarPubMed
Chavez, F.P., Messié, M. and Pennington, J.T. (2011) Marine primary production in relation to climate variability and change. Annual Review of Marine Science 3, 227260.Google Scholar
Chen, S. and Gao, K. (2011) Solar ultraviolet radiation and CO2-induced ocean acidification interacts to influence the photosynthetic performance of the red tide alga Phaeocystis globosa (Prymnesiophyceae). Hydrobiologia 675, 105117.Google Scholar
Chen, X. and Gao, K. (2004) Characterization of diurnal photosynthetic rhythms in the marine diatom Skeletonema costatum grown in synchronous culture under ambient and elevated CO2 . Functional Plant Biology 31, 399404.Google Scholar
Collins, S., Sueltemeyer, D. and Bell, G. (2006) Changes in C uptake in populations of Chlamydomonas reinhardtii selected at high CO2 . Plant, Cell and Environment 29, 18121819.CrossRefGoogle Scholar
Crawley, A., Kline, D.I., Dunn, S., Anthony, K. and Dove, S. (2010) The effect of ocean acidification on symbiont photorespiration and productivity in Acropora formosa . Global Change Biology 16, 851863.Google Scholar
Davis, A.R., Coleman, D., Broad, A., Byrne, M., Dworjanyn, S.A. and Przeslawski, R. (2013) Complex responses of intertidal molluscan embryos to a warming and acidifying ocean in the presence of UV radiation. PLoS ONE 8, e55939.Google Scholar
Flynn, K.J., Blackford, J.C., Baird, M.E., Raven, J.A., Clark, D.R., Beardall, J., Brownlee, C., Fabian, H. and Wheeler, G.L. (2012) Changes in pH at the exterior surface of plankton with ocean acidification. Nature Climate Change 2, 510513.Google Scholar
Gao, K., Helbling, E.W., Haeder, D.-P. and Hutchins, D.A. (2012a) Responses of marine primary producers to interactions between ocean acidification, solar radiation, and warming. Marine Ecology Progress Series 470, 167189.Google Scholar
Gao, K., Xu, J., Gao, G., Li, Y., Hutchins, D.A., Huang, B., Wang, L., Zheng, Y., Jin, P., Cai, X., Häder, D.-P., Li, W., Xu, K., Liu, N. and Riebesell, U. (2012b) Rising CO2 and increased light exposure synergistically reduce marine primary productivity. Nature Climate Change 2, 519523.Google Scholar
Genty, B., Harbinson, J. and Baker, N. (1990) Relative quantum efficiencies of the two photosystems of leaves in photorespiratory and non-respiratory conditions. Plant Physiology and Biochemistry (Paris) 28, 110.Google Scholar
Giordano, M., Beardall, J. and Raven, J.A. (2005) CO2 concentrating mechanisms in algae: mechanisms, environmental modulation, and evolution. Annual Review of Plant Biology 56, 99131.Google Scholar
Guan, W. and Gao, K. (2008) Light histories influence the impacts of solar ultraviolet radiation on photosynthesis and growth in a marine diatom, Skeletonema costatum . Journal of Photochemistry and Photobiology B: Biology 91, 151156.Google Scholar
Guan, W. and Gao, K. (2010) Impacts of UV radiation on photosynthesis and growth of the coccolithophore Emiliania huxleyi (Haptophyceae). Environmental and Experimental Botany 67, 502508.Google Scholar
Guan, W., Li, P., Jian, J., Wang, J. and Lu, S. (2011) Effects of solar ultraviolet radiation on photochemical efficiency of Chaetoceros curvisetus (Bacillariophyceae). Acta Physiologiae Plantarum 33, 979986.CrossRefGoogle Scholar
Guan, W. and Lu, S. (2010) The short-and long-term response of Scrippsiella trochoidea (Pyrrophyta) to solar ultraviolet radiation. Photosynthetica 48, 287293.Google Scholar
Guillard, R.R. and Ryther, J.H. (1962) Studies on marine planktonic diatoms. I. Cyclotella nana (Hustedt) and Detonula confervaceae (Cleve). Canadian Journal of Microbiology 8, 229239.Google Scholar
Häder, D.-P. (2011) Does enhanced solar UV-B radiation affect marine primary producers in their natural habitats? Photochemistry and Photobiology 87, 263266.CrossRefGoogle ScholarPubMed
Häder, D.-P., Kumar, H., Smith, R. and Worrest, R. (2007) Effects of solar UV radiation on aquatic ecosystems and interactions with climate change. Photochemical and Photobiological Sciences 6, 267285.Google Scholar
Häder, D.-P., Lebert, M., Marangoni, R. and Colombetti, G. (1999) ELDONET –European light dosimeter network hardware and software. Journal of Photochemistry and Photobiology B: Biology 52, 5158.CrossRefGoogle Scholar
Hughes, L. (2000) Biological consequences of global warming: is the signal already apparent? Trends in Ecology and Evolution 15, 5661.Google Scholar
Jassby, A.D. and Platt, T. (1976) Mathematical formulation of the relationship between photosynthesis and light for phytoplankton. Limnology and Oceanography 21, 540547.Google Scholar
Koch, M., Bowes, G., Ross, C. and Zhang, X.H. (2013) Climate change and ocean acidification effects on seagrasses and marine macroalgae. Global Change Biology 19, 103132.CrossRefGoogle ScholarPubMed
Kroeker, K.J., Kordas, R.L., Crim, R., Hendriks, I.E., Ramajo, L., Singh, G.S., Duarte, C.M. and Gattuso, J.-P. (2013) Impacts of ocean acidification on marine organisms: quantifying sensitivities and interaction with warming. Global Change Biology 19, 18841896.Google Scholar
Li, Y., Gao, K., Villafañe, V. and Helbling, E. (2012) Ocean acidification mediates photosynthetic response to UV radiation and temperature increase in the diatom Phaeodactylum tricornutum . Biogeosciences Discussions 9, 71977226.Google Scholar
Liang, Y., Beardall, J. and Heraud, P. (2006) Effect of UV radiation on growth, chlorophyll fluorescence and fatty acid composition of Phaeodactylum tricornutum and Chaetoceros muelleri (Bacillariophyceae). Journal of Photochemistry and Photobiology B: Biology 82, 161172.Google Scholar
Mathis, J.T., Cross, J.N. and Bates, N.R. (2011). Coupling primary production and terrestrial runoff to ocean acidification and carbonate mineral suppression in the eastern Bering Sea. Journal of Geophysical Research: Oceans 116, C02030.Google Scholar
Millero, F.J. (1995) Thermodynamics of the carbon dioxide system in the oceans. Geochimica et Cosmochimica Acta 59, 661677.Google Scholar
Porra, R.J. (2005) The chequered history of the development and use of simultaneous equations for the accurate determination of chlorophylls a and b. Advances in Photosynthesis and Respiration 20, 633640.Google Scholar
Riebesell, U., Wolf-Gladrow, D. and Smetacek, V. (1993) Carbon dioxide limitation of marine phytoplankton growth rates. Nature 361, 249251.CrossRefGoogle Scholar
Rost, B., Riebesell, U., Burkhardt, S. and Sültemeyer, D. (2003) Carbon acquisition of bloom-forming marine phytoplankton. Limnology and Oceanography 48, 5567.Google Scholar
Sobrino, C., Neale, P.J. and Lubián, L.M. (2005) Interaction of UV radiation and inorganic carbon supply in the inhibition of photosynthesis: spectral and temporal responses of two marine picoplankters. Photochemistry and Photobiology 81, 384393.CrossRefGoogle ScholarPubMed
Sobrino, C., Ward, M.L. and Neale, P.J. (2008) Acclimation to elevated carbon dioxide and ultraviolet radiation in the diatom Thalassiosira pseudonana: effects on growth, photosynthesis, and spectral sensitivity of photoinhibition. Limnology and Oceanography 53, 494.Google Scholar
Turley, C., Blackford, J., Widdicombe, S., Lowe, D., Nightingale, P. and Rees, A. (2006) Reviewing the impact of increased atmospheric CO2 on oceanic pH and the marine ecosystem. In Schellnhuber, H.J., Cramer, W., Nakicenovic, N., Wigley, T. and Yohe, G. (eds) Avoiding Dangerous Climate Change. Cambridge: Cambridge University Press, pp. 6570.Google Scholar
van Rijssel, M. and Buma, A.G. (2002) UV radiation induced stress does not affect DMSP synthesis in the marine prymnesiophyte Emiliania huxleyi . Aquatic Microbial Ecology 28, 167174.Google Scholar
Wang, X.-l., Yang, R.-j. and Zhu, C.-J. (2004) Studies on size effect on Chaetoceros curvisetus in different concentrations of petroleum hydrocarbon. Journal of Ocean University of Qingdao 5, 27.Google Scholar
Wu, X., Gao, G., Giordano, M. and Gao, K. (2012) Growth and photosynthesis of a diatom grown under elevated CO2 in the presence of solar UV radiation. Fundamental and Applied Limnology/Archiv für Hydrobiologie 180, 279290.CrossRefGoogle Scholar
Wu, Y., Gao, K. and Riebesell, U. (2010) CO2-induced seawater acidification affects physiological performance of the marine diatom Phaeodactylum tricornutum . Biogeosciences Discussions 7, 38553878.Google Scholar
Xiong, F. (2001) Evidence that UV-B tolerance of the photosynthetic apparatus in microalgae is related to the D1-turnover mediated repair cycle in vivo . Journal of Plant Physiology 158, 285294.Google Scholar
Zheng, Y. and Gao, K. (2009). Impacts of solar UV radiation on the photosynthesis, growth, and UV-absorbing compounds in Gracilaria lemaneiformis (Rhodophyta) grown at different nitrate concentrations. Journal of Phycology 45, 314323.Google Scholar