Skip to main content
Log in

UV-screening of grasses by plant silica layer?

  • Mini-review
  • Published:
Journal of Biosciences Aims and scope Submit manuscript

Abstract

UV-screening by terrestrial plants is a crucial trait since colonization of terrestrial environments has started. In general, it is enabled by phenolic substances. Especially for grasses it remains unclear why plants grown under the absence of UV-B-radiation exhibit nonetheless a high UV-B-screening potential. But this may be explained by the UV-screening effect of the silicon double layer. It was shown for seedlings of soybeans (Glycine max L.) and wheat (Triticum aestivum L.) that enhanced silicon supply reduces stress induced by UV-radiation. Even more important is a direct correlation between silicon content in the epidermis near area (intercellular spaces) and the absorption of UV-radiation in this area shown in other papers. The silicon double layer may act like a glass layer and decreases the transmission of UV-radiation at the epidermis near area. In summary, the absorbance/reflection of ultraviolet radiation is dependent on the characteristics of the epidermis near area of leaves, particularly the occurrence (qualitatively and quantitatively) of phenolic substances and/or a silicon double layer in this area. Consequently, UV-screening by plant silicon double layer should get more attention in future research with emphasis on effects of UV-radiation on plant physiology.

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.

Figure 1

Similar content being viewed by others

References

  • Cocker KM, Evans DE and Hodson MJ 1998 The amelioration of aluminium toxicity by silicon in wheat (Triticum aestivum L.): malate exudation as evidence for an in planta mechanism. Planta 204 318–323

    Article  CAS  Google Scholar 

  • Cooke J and Leishman MR 2011a Is plant ecology more siliceous than we realise? Trends Plant Sci. 16 61–68

  • Cooke J and Leishman MR 2011b Silicon concentration and leaf longevity: is silicon a player in the leaf dry mass spectrum? Funct. Ecol. 25 1181–1188

    Article  Google Scholar 

  • Cooper-Driver GA and Bhattacharya M 1998 Role of phenolics in plant evolution. Phytochemistry 49 1165–1174

    Article  CAS  Google Scholar 

  • Cornelis JT, Delvaux B, Cardinal D, Andre L, Ranger J and Opfergelt S 2010 Tracing mechanisms controlling the release of dissolved silicon in forest soil solutions using Si isotopes and Ge/Si ratios. Geochimica Et Cosmochimica Acta 74 3913–3924

    Article  CAS  Google Scholar 

  • Currie HA and Perry CC 2007 Silica in plants: Biological, biochemical and chemical studies. Ann. Bot. 100 1383–1389

    Article  PubMed  CAS  Google Scholar 

  • Derry LA, Kurtz AC, Ziegler K and Chadwick OA 2005 Biological control of terrestrial silica cycling and export fluxes to watersheds. Nature 433 728–731

    Article  PubMed  CAS  Google Scholar 

  • Eneji AE, Inanaga S, Muranaka S, Li J, Hattori T, An P and Tsuji W 2008 Growth and nutrient use in four grasses under drought stress as mediated by silicon fertilizers. J. Plant Nutr. 31 355–365

    Google Scholar 

  • Epstein E 1999 Silicon. Annu. Rev. Plant Physiol. Plant Mol. Biol. 50 641–664

  • Fang JY, Wan XC and Ma XL 2006 Nanoscale silicas in Oryza sativa L. and their UV absorption. Spectroscopy Spectral Anal. 26 2315–2318

    Google Scholar 

  • Fawe A, Abou-Zaid M, Menzies JG and Belanger RR 1998 Silicon-mediated accumulation of flavonoid phytoalexins in cucumber. Phytopathology 88 396–401

    Article  PubMed  CAS  Google Scholar 

  • Gatto A, Escoubas L, Roche P and Commandre M 1998 Simulation of the degradation of optical glass substrates caused by UV irradiation while coating. Optics Commun. 148 347–354

  • Goto M, Ehara H, Karita S, Takabe K, Ogawa N, Yamada Y, Ogawa S, Yahaya MS and Morita O 2003 Protective effect of silicon on phenolic biosynthesis and ultraviolet spectral stress in rice crop. Plant Sci. 164 349–356

  • Hodson MJ and Sangster AG 1988 Observations on the distribution of mineral elements in the leaf of wheat (Triticum aestivum L), with particular reference to silicon. Ann. Bot. 62 463–471

    Google Scholar 

  • Hodson MJ, White PJ, Mead A and Broadley MR 2005 Phylogenetic variation in the silicon composition of plants. Ann. Bot. 96 1027–1046

    Article  PubMed  CAS  Google Scholar 

  • Kitamura R, Pilon L and Jonasz M 2007 Optical constants of silica glass from extreme ultraviolet to far infrared at near room temperature. Appl. Optics 46 8118–8133

    Google Scholar 

  • Liang YC, Sun WC, Zhu YG and Christie P 2007 Mechanisms of silicon-mediated alleviation of abiotic stresses in higher plants: A review. Environ. Pollut. 147 422–428

    Article  PubMed  CAS  Google Scholar 

  • Ma JF and Yamaji N 2006 Silicon uptake and accumulation in higher plants. Trends Plant Sci. 11 392–397

    Google Scholar 

  • Ma JF, Tamai K, Yamaji N, Mitani N, Konishi S, Katsuhara M, Ishiguro M, Murata Y and Yano M 2006 A silicon transporter in rice. Nature 440 688–691

    Article  PubMed  CAS  Google Scholar 

  • Massey FP and Hartley SE 2009 Physical defences wear you down: progressive and irreversible impacts of silica on insect herbivores. J. Animal Ecol. 78 281–291

    Google Scholar 

  • McNaughton SJ and Tarrants JL 1983 Grass leaf silicification - natural-selection for an inducible defence against herbivores. Proc. Natl. Acad. Sci. USA – Biol. Sci. 80 790–791

  • Melzer SE, Knapp AK, Kirkman KP, Smith MD, Blair JM and Kelly EF 2010 Fire and grazing impacts on silica production and storage in grass dominated ecosystems. Biogeochemistry 97 263–278

    Article  CAS  Google Scholar 

  • Neumann D and zur Nieden U 2001 Silicon and heavy metal tolerance of higher plants. Phytochemistry 56 685–692

    Google Scholar 

  • Rozema J, vandeStaaij J, Bjorn LO and Caldwell M 1997 UV-B as an environmental factor in plant life: Stress and regulation. Trends Ecol. Evol. 12 22–28

    Google Scholar 

  • Schaller J, Brackhage C and Dudel E 2012a Silicon availability changes structural carbon ratio and phenol content of grasses. Environ. Exp. Bot. 77 283–287

    Article  CAS  Google Scholar 

  • Schaller J, Brackhage C, Gessner MO, Bäuker E and Gert Dudel E 2012b Silicon supply modifies C:N:P stoichiometry and growth of Phragmites australis. Plant Biol. 14 392–396

  • Schaller J, Brackhage C, Paasch S, Brunner E, Bäucker E and Dudel EG 2013 Silica uptake from nanoparticles and silica condensation state in different tissues of Phragmites australis. Sci. Total Environ. 442 6–9

    Google Scholar 

  • Schmitz-Hoerner R and Weissenbock G 2003 Contribution of phenolic compounds to the UV-B screening capacity of developing barley primary leaves in relation to DNA damage and repair under elevated UV-B levels. Phytochemistry 64 243–255

    Article  PubMed  CAS  Google Scholar 

  • Schoelynck J, Bal K, Backx H, Okruszko T, Meire P and Struyf E 2010 Silica uptake in aquatic and wetland macrophytes: a strategic choice between silica, lignin and cellulose? New Phytol. 186 385–391

  • Shen XF, Zhou YY, Duan LS, Li ZH, Eneji AE and Li JM 2010 Silicon effects on photosynthesis and antioxidant parameters of soybean seedlings under drought and ultraviolet-B radiation. J. Plant Physiol. 167 1248–1252

    Google Scholar 

  • Struyf E and Conley DJ 2009 Silica: an essential nutrient in wetland biogeochemistry. Front. Ecol. Environ. 7 88–94

    Article  Google Scholar 

  • Treutter D 2005 Significance of flavonoids in plant resistance and enhancement of their biosynthesis. Plant Biol. 7 581–591

  • Tuchinda C, Srivannaboon S and Lim HW 2006 Photoprotection by window glass, automobile glass, and sunglasses. J. Am. Acad. Dermatol. 54 845–854

    Article  PubMed  Google Scholar 

  • Webb EA and Longstaffe FJ 2000 The oxygen isotopic compositions of silica phytoliths and plant water in grasses: Implications for the study of paleoclimate. Geochimica Et Cosmochimica Acta 64 767–780

    Article  CAS  Google Scholar 

  • Winkel-Shirley B 2002 Biosynthesis of flavonoids and effects of stress. Curr. Opin. Plant Biol. 5 218–223

    Google Scholar 

  • Yao XQ, Chu JZ, Cai KZ, Liu L, Shi JD and Geng WY 2011 Silicon improves the tolerance of wheat seedlings to ultraviolet-B stress. Biol. Trace Element Res. 143 507–517

    Google Scholar 

  • Zimmermann F, Opfermann M, Bäucker E, Fiebig J and Nebe W 2000 Nutrition-physiological responses of spruce to different levels of sulphur dioxide stress in the Erzgebirge Mountains and the Thuringian Forest, Germany. Forstwissenschaftliches Centralblatt 119 193–207

    Article  CAS  Google Scholar 

Download references

Acknowledgements

The authors thank Mrs Julia Senft (Burg Giebichenstein Kunsthochschule Halle, Germany) for drafting the figure scheme.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jörg Schaller.

Additional information

Corresponding editor: MAN MOHAN JOHRI

[Schaller J, Brackhage C, Bäucker E and Dudel E G 2013 UV-screening of grasses by plant silica layer? J. Biosci. 38 1–4] DOI 10.1007/s12038-013-9303-1

Rights and permissions

Reprints and permissions

About this article

Cite this article

Schaller, J., Brackhage, C., Bäucker, E. et al. UV-screening of grasses by plant silica layer?. J Biosci 38, 413–416 (2013). https://doi.org/10.1007/s12038-013-9303-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12038-013-9303-1

Keywords

Navigation