Skip to main content

Advertisement

Log in

Altered seawater salinity levels affected growth and photosynthesis of Ulva fasciata (Ulvales, Chlorophyta) germlings

  • Published:
Acta Oceanologica Sinica Aims and scope Submit manuscript

Abstract

Seawater salinity is greatly influenced by tide, evaporation and rain falls. In this study, we investigated the growth and photosynthetic responses of zygote-derived Ulva fasciata Delile germlings to short-term (minutes) and prolonged (days) exposure to different salinity gradients, to evaluate the effect of salinity variation on the early stage of life history in this seaweed. The results showed that, the maximum net photosynthetic rates (NPRm) of U. fasciata germlings was observably decreased in desalted (25 and 15) and high (45) salinity seawater in short-term exposure tests (in minutes). However, after 30 min, the photosynthesis activity in medium salinity (25) was maintained at a relative high level (above 70%). After 8 d prolonged culture, the photosynthesis and mean relative growth rate (RGR) of germlings were all markedly lowered, whereas the malondialdehyde (MDA) contents increased as the salinity desalted from 34 to 15. The salinity decrease from 34 to 25 had no significant effect on the RGR, but obviously influenced the morphology of the germlings. High salinity level (45) significantly depressed the RGR and photosynthesis of U. fasciata germlings, while it notably increased the MDA contents. The results showed that the salinity elevation had more detrimental effects on Ulva fasciata germlings than salinity decrease did. The germlings grown at the salinity seawater levels from 25 to 34, performed preferable photosynthetic acclimation both in temporary and prolonged culture. Broad salinity tolerance from 25 to 34 in U. fasciata germlings may have partly evolved as a response to regular diurnal tides.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Ahmad I, Hellebust J A. 1988. The relationship between inorganic nitrogen metabolism and proline accumulation in osmoregulatory responses of two euryhaline microalgae. Plant Physiology, 88(2): 348–354

    Article  Google Scholar 

  • Bisson M A, Kirst G O. 1979. Osmotic adaption in the marine alga Griffithsia monilis (Rhodophyceae): the role of ions and organic compounds. Australian Journal of Plant Physiology, 6(4): 523–538

    Google Scholar 

  • Bowler C, van Montagu M, Inze D. 1992. Superoxide dismutase and stress tolerance. Annual Review of Plant Physiology and Plant Molecular Biology, 43: 83–116

    Article  Google Scholar 

  • Chang W-C, Chen M-H, Lee T-M. 1999. 2, 3, 5 triphenyltetrazolium chloride reduction in the viability assay of Ulva fasciata (Chlorophyta) in response to salinity stress. Botanical Bulletin Academia Sinica, 40: 207–212

    Google Scholar 

  • Corney H J, Sasse J M, Ades P K. 2003. Assessment of salt tolerance in eucalypts using chlorophyll fluorescence attributes. New Forests, 26(3): 233–246

    Article  Google Scholar 

  • Davison I R, Pearson G A. 1996. Stress tolerance in intertidal seaweeds. Journal of Phycology, 32(2): 197–211

    Article  Google Scholar 

  • Dawes C J. 1998. Marine Botany. 2nd ed. New York: John Wiley & Sons, Inc, 82–85

    Google Scholar 

  • Dickson D M, Wyn Jones R G, Davenport J. 1980. Steady state osmotic adaptation in Ulva lactuca. Planta, 150(2): 158–165

    Article  Google Scholar 

  • Durack P J, Wijffels S E, Matear R J. 2012. Ocean salinities reveal strong global water cycle intensification during 1950 to 2000. Science, 336(6080): 455–458

    Article  Google Scholar 

  • Florides G A, Christodoulides P. 2009. Global warming and carbon dioxide through sciences. Environment International, 35(2): 390–401

    Article  Google Scholar 

  • Gessner E, Schramm W. 1971. Salinity: plants. In: Kinne O, ed. Marine Ecology. Volume 1. London: Wiley-Interscience, 705–720

    Google Scholar 

  • González-Moreno S, Gómez-Barrera J, Perales H, et al. 1997. Multiple effects of salinity on photosynthesis of the protist Euglena gracilis. Physiologia Plantarum, 101(4): 777–786

    Article  Google Scholar 

  • Heath R L, Packer L. 1968. Photoperoxidation in isolated chloroplasts: I. Kinetics and stoichiometry of fatty acid peroxidation. Archives of Biochemistry and Biophysics, 125(1): 189–198

    Article  Google Scholar 

  • Hellebust J A. 1976. Effect of salinity on photosynthesis and mannitol synthesis in the green flagellate Platymonas suecica. Canadian Journal of Botany, 54(15): 1735–1741

    Article  Google Scholar 

  • Henley W J. 1993. Measurement and interpretation of photosynthetic light-response curves in algae in the context of photoinhibition and diel changes. Journal of Phycology, 29(6): 729–739

    Article  Google Scholar 

  • Hiraoka M, Oka N. 2008. Tank cultivation of Ulva prolifera in deep seawater using a new “germling cluster” method. Journal of Applied Phycology, 20(1): 97–102

    Article  Google Scholar 

  • Huang Qing, Shen Hanming. 2009. To die or to live: the dual role of poly (ADP-ribose) polymerase-1 in autophagy and necrosis under oxidative stress and DNA damage. Autophagy, 5(2): 273–276

    Article  Google Scholar 

  • IPCC (Intergovernmental Panel on Climate Change). 2007. Climate Change 2007: Synthesis Report. Cambridge, UK: Cambridge University Press

  • Lartigue J, Neill A, Hayden B L, et al. 2003. The impact of salinity fluctuations on net oxygen production and inorganic nitrogen uptake by Ulva lactuca (Chlorophyceae). Aquatic Botany, 75(4): 339–350

    Article  Google Scholar 

  • Lee Y-H, Kim D-J, Kim H-K. 2003. Characteristics of the seawater quality variation on the South Coastal Area of Korea. KSCE Journal of Civil Engineering, 7(2): 123–130

    Article  Google Scholar 

  • Liu Jingwen, Dong Shuangxiu, Ma Shen. 2001. Effects of temperature and salinity on growth of G. tenuistipitata var. liui, U. pertusa, G. filicina and NH4-N uptake of G. tenuistipitata var. liui. Haiyang Xuebao (in Chinese), 23(2): 109–116

    Google Scholar 

  • Lu Congming, Vonshak A. 2002. Effects of salinity stress on photosystem II function in cyanobacterial Spirulina platensis cells. Physiologia Plantarum, 114(3): 405–413

    Article  Google Scholar 

  • Mantri V A, Singh R P, Bijo A J, et al. 2011. Differential response of varying salinity and temperature on zoospore induction, regeneration and daily growth rate in Ulva fasciata (Chlorophyta, Ulvales). Journal of Applied Phycology, 23(2): 243–250

    Article  Google Scholar 

  • Ohno M. 2006. Recent developments in the seaweed cultivation and industry in Japan. In: Phang S M, Critchley A T, Ang P O, et al., eds. Advances in Seaweed Cultivation and Utilisation in Asia. Kuala Lumpur: University of Malaya Maritime Research Center, 1–20

    Google Scholar 

  • Richter M, Rühle W, Wild A. 1990. Studies on the mechanism of photosystem II photoinhibition I. A two-step degradation of D1-protein. Photosynthesis Research, 24(3): 229–235

    Article  Google Scholar 

  • Satoh K, Smith C M, Fork D C. 1983. Effects of salinity on primary processes of photosynthesis in the red alga Porphyra perforata. Plant Physiology, 73(3): 643–647

    Article  Google Scholar 

  • Schmitt R W. 1996. If rain falls on the ocean-does it make a sound? Fresh water's effect on ocean phenomena. Oceanus, 39(2): 4–8

    Google Scholar 

  • Steen H. 2004. Effects of reduced salinity on reproduction and germling development in Sargassum muticum (Phaeophyceae, Fucales). European Journal of Phycology, 39(3): 293–299

    Article  Google Scholar 

  • Wong C-L, Phang S-M. 2004. Biomass production of two Sargassum species at Cape Rachado, Malaysia. Hydrobiologia, 512(1–3): 79–88

    Article  Google Scholar 

  • Xia Jianrong, Li Yongjun, Zou Dinghui. 2004. Effects of salinity stress on PSII in Ulva lactuca as probed by chlorophyll fluorescence measurements. Aquatic Botany, 80(2): 129–137

    Article  Google Scholar 

  • Yamochi S. 2013. Effects of desiccation and salinity on the outbreak of a green tide of Ulva pertusa in a created salt marsh along the coast of Osaka Bay, Japan. Estuarine, Coastal and Shelf Science, 116: 21–28

    Article  Google Scholar 

  • Ying Weihai, Alano C C, Garnier P, et al. 2005. NAD+ as a metabolic link between DNA damage and cell death. Journal of Neuroscience Research, 79(1–2): 216–223

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Dinghui Zou.

Additional information

Foundation item: The National Natural Science Foundation of China under contract Nos 41276148 and 41076094.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chen, B., Zou, D. Altered seawater salinity levels affected growth and photosynthesis of Ulva fasciata (Ulvales, Chlorophyta) germlings. Acta Oceanol. Sin. 34, 108–113 (2015). https://doi.org/10.1007/s13131-015-0654-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s13131-015-0654-3

Keywords

Navigation