Skip to main content
Log in

Silicification patterns in wheat leaves related to ontogeny and soil silicon availability under field conditions

  • Regular Article
  • Published:
Plant and Soil Aims and scope Submit manuscript

Abstract

Purpose

Silicon (Si) accumulation is an important strategy for plant defense against biotic and abiotic stress. Solid amorphous silica (ASi) deposits have been found to protect plants against different stressors (e.g., drought stress, ultraviolet radiation, herbivory, and pests). Most research on ASi deposits and their subsequent function is conducted under lab conditions. However, it is still unclear at which stage in ontogeny ASi deposits are developed to fulfill their function in plant protection under field conditions.

Methods

We combined SEM–EDX, NMR spectroscopy, and Si extractions to analyze silicification patterns in wheat leaves (blades and sheaths) in relation to ontogeny and soil Si availability.

Results

Silicification patterns in wheat leaves varied strongly in intensity between four different growth stages (tillering, stem extension, heading, and grain filling) and ASi deposition did not just continuously increase over the growing season. Newly formed leaf tissues showed relatively low Si concentrations, which increased over time. A high condensation state of the silica bodies and trichomes was found at all growth stages, referring to a high rigidity of the silica bodies.

Conclusions

Our results indicate that development of ASi deposits in wheat leaves depends on growth stage and Si availability. Detailed knowledge on solid ASi deposition in wheat during ontogeny and its consequences for stress mitigation is crucial for farmers worldwide.

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.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5
Fig. 6
Fig. 7
Fig. 8
Fig. 9

Similar content being viewed by others

Data availability

The data that support the findings of this study are available from the corresponding author upon reasonable request.

References

  • Agarie S, Agata W, Uchida H, Kubota F, Kaufman PB (1996) Function of silica bodies in the epidermal system of rice (Oryza sativa L.): testing the window hypothesis. J Exp Bot 47:655–660

    Article  CAS  PubMed  Google Scholar 

  • Alexieva V, Sergiev I, Mapelli S, Karanov E (2001) The effect of drought and ultraviolet radiation on growth and stress markers in pea and wheat. Plant, Cell Environ 24:1337–1344

    Article  CAS  Google Scholar 

  • Boege K (2005) Herbivore attack in Casearia nitida influenced by plant ontogenetic variation in foliage quality and plant architecture. Oecologia 143:117–125

    Article  PubMed  Google Scholar 

  • Bolhàr-Nordenkampf HR, Draxler G (1993) Functional leaf anatomy. In: DO Hall, JMO Scurlock, HR Bolhàr-Nordenkampf, RC Leegood, SP Long (eds) Photosynthesis and Production in a Changing Environment: A field and laboratory manual. Springer Netherlands, Dordrecht

  • Clarke AR, Zalucki MP (2000) Foraging and vein-cutting behaviour of Euploea core corinna (WS Macleay)(Lepidoptera: Nymphalidae) caterpillars feeding on latex-bearing leaves. Aust J Entomol 39:283–290

    Article  Google Scholar 

  • Cooke J, Leishman MR (2012) Tradeoffs between foliar silicon and carbon-based defences: evidence from vegetation communities of contrasting soil types. Oikos 121:2052–2060

    Article  Google Scholar 

  • Cooke J, Leishman MR (2016) Consistent alleviation of abiotic stress with silicon addition: a meta-analysis. Funct Ecol 30:1340–1357

    Article  Google Scholar 

  • Deshmukh R, Bélanger RR (2016) Molecular evolution of aquaporins and silicon influx in plants. Funct Ecol 30:1277–1285

    Article  Google Scholar 

  • Epstein E (1999) Silicon. Annu Rev Plant Physiol Plant Molec Biol 50:641–664

    Article  CAS  Google Scholar 

  • Fauteux F, Remus-Borel W, Menzies JG, Belanger RR (2005) Silicon and plant disease resistance against pathogenic fungi. FEMS Microbiol Lett 249:1–6

    Article  CAS  PubMed  Google Scholar 

  • Fung BM, Khitrin AK, Ermolaev K (2000) An improved broadband decoupling sequence for liquid crystals and solids. J Magn Reson 142:97–101

    Article  CAS  PubMed  Google Scholar 

  • Gao X, Zou C, Wang L, Zhang F (2006) Silicon decreases transpiration rate and conductance from stomata of maize plants. J Plant Nutr 29:1637–1647

    Article  CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Hall CR, Dagg V, Waterman JM, Johnson SN (2020) Silicon alters leaf surface morphology and suppresses insect herbivory in a model grass species. Plants 9:643

    Article  CAS  PubMed Central  Google Scholar 

  • Hartley SE, Fitt RN, McLarnon EL, Wade RN (2015) Defending the leaf surface: intra-and inter-specific differences in silicon deposition in grasses in response to damage and silicon supply. Front Plant Sci 6:35

    Article  PubMed  PubMed Central  Google Scholar 

  • Hodson MJ, 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

    Article  Google Scholar 

  • Katz O (2019) Silicon content is a plant functional trait: implications in a changing world. Flora 254:88–94

    Article  Google Scholar 

  • Katz O (2020) Silicon and Plant-Animal Interactions: Towards an Evolutionary Framework. Plants 9:430

    Article  PubMed Central  Google Scholar 

  • Katz O, Lev-Yadun S, Bar P (2018) Plant silicon and phytolith contents as affected by water availability and herbivory: integrating laboratory experimentation and natural habitat studies. SILICON 10:2387–2389

    Article  CAS  Google Scholar 

  • Katz O, Puppe D, Kaczorek D, Prakash NB, Schaller J (2021) Silicon in the Soil-Plant Continuum: Intricate Feedback Mechanisms within Ecosystems. Plants 10:652

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kempe A, Sommer M, Neinhuis C (2013) A Comparative Analysis of the Mechanical Role of Leaf Sheaths of Poaceae, Juncaceae, and Cyperaceae. Journal of Botany.

  • Klotzbücher T, Klotzbücher A, Kaiser K, Vetterlein D, Jahn R, Mikutta R (2018) Variable silicon accumulation in plants affects terrestrial carbon cycling by controlling lignin synthesis. Glob Change Biol 24:e183–e189

    Article  Google Scholar 

  • Kumar S, Milstein Y, Brami Y, Elbaum M, Elbaum R (2017a) Mechanism of silica deposition in sorghum silica cells. New Phytol 213:791–798

    Article  CAS  PubMed  Google Scholar 

  • Kumar S, Soukup M, Elbaum R (2017b) Silicification in grasses: variation between different cell types. Front Plant Sci 8:438

    PubMed  PubMed Central  Google Scholar 

  • Liang YC, Hua HX, Zhu YG, Zhang J, Cheng CM, Romheld V (2006) Importance of plant species and external silicon concentration to active silicon uptake and transport. New Phytol 172:63–72

    Article  CAS  PubMed  Google Scholar 

  • Ma JF, Yamaji N (2015) A cooperated system of silicon transport in plants. Trends Plant Sci 20:435–442

    Article  CAS  PubMed  Google Scholar 

  • Massey FP, Ennos AR, Hartley SE (2007) Herbivore specific induction of silica-based plant defences. Oecologia 152:677–683

    Article  PubMed  Google Scholar 

  • Miliarakis S (1884) Die Verkieselung lebender Elementarorgane bei den Pflanzen

  • Mitani N, Ma JF (2005) Uptake system of silicon in different plant species. J Exp Bot 56:1255–1261

    Article  CAS  PubMed  Google Scholar 

  • Neu S, Schaller J, Dudel EG (2017) Silicon availability modifies nutrient use efficiency and content, C:N:P stoichiometry, and productivity of winter wheat (Triticum aestivum L.). Scientific Reports 7: 40829

  • Pierantoni M, Tenne R, Brumfeld V, Kiss V, Oron D, Addadi L, Weiner S (2017) Plants and light manipulation: the integrated mineral system in okra leaves. Advanced Science 4:1600416

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Potter DA, Kimmerer TW (1988) Do holly leaf spines really deter herbivory? Oecologia 75:216–221

    Article  PubMed  Google Scholar 

  • Puppe D, Kaczorek D, Schaller J, Barkusky D, Sommer M (2021) Crop straw recycling prevents anthropogenic desilication of agricultural soil-plant systems in the temperate zone – Results from a long-term field experiment in NE Germany. Geoderma 403:115187

    Article  CAS  Google Scholar 

  • Reynolds OL, Keeping MG, Meyer JH (2009) Silicon-augmented resistance of plants to herbivorous insects: a review. Ann Appl Biol 155:171–186

    Article  CAS  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Schaller J, Brackhage C, Bäucker E, Dudel EG (2013a) UV-screening of grasses by plant silica layer? J Biosci 38:413–416

    Article  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Schaller J, Heimes R, Ma JF, Meunier J-D, Shao JF, Fujii-Kashino M, Knorr KH (2019) Silicon accumulation in rice plant aboveground biomass affects leaf carbon quality. Plant Soil 444:399–407

    Article  CAS  Google Scholar 

  • Schaller J, Puppe D, Kaczorek D, Ellerbrock R, Sommer M (2021) Silicon Cycling in Soils Revisited Plants 10:295

    CAS  PubMed  Google Scholar 

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

    Article  CAS  PubMed  Google Scholar 

  • Strasburger E, Noll F, Schenck H, Schimper AFW (1962) Lehrbuch der Botanik. Auflage Stuttgart: 732

  • Teixeira NC, Valim JOS, Campos WG (2017) Silicon-mediated resistance against specialist insects in sap-sucking and leaf-chewing guilds in the Si non-accumulator collard. Entomol Exp Appl 165:94–108

    Article  CAS  Google Scholar 

  • de Tombeur F, Roux P, Cornelis J-T (2021) Silicon dynamics through the lens of soil-plant-animal interactions: perspectives for agricultural practices. Plant Soil: 1–28

  • Trembath-Reichert E, Wilson JP, McGlynn SE, Fischer WW (2015) Four hundred million years of silica biomineralization in land plants. Proc Natl Acad Sci 112:5449–5454

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Ueno O, Agarie S (2005) Silica deposition in cell walls of the stomatal apparatus of rice leaves. Plant Production Science 8:71–73

    Article  Google Scholar 

  • Vandegeer RK, Zhao C, Cibils‐Stewart X, Wuhrer R, Hall CR, Hartley SE, Tissue DT, Johnson SN (2020) Silicon deposition on guard cells increases stomatal sensitivity as mediated by K+ efflux and consequently reduces stomatal conductance. Physiol Plant

  • Wang M, Gao L, Dong S, Sun Y, Shen Q, Guo S (2017) Role of silicon on plant–pathogen interactions. Front Plant Sci 8:701

    Article  PubMed  PubMed Central  Google Scholar 

  • Waterman JM, Hall CR, Mikhael M, Cazzonelli CI, Hartley SE, Johnson SN (2020) Short‐term resistance that persists: Rapidly induced silicon anti‐herbivore defence affects carbon‐based plant defences. Funct Ecol

Download references

Acknowledgements

Special thanks to Sven Schnabel, Frank Gesper, and Uwe Busse (Experimental Infrastructure Platform, ZALF) for setting up and managing the experiment, and to the team of the central laboratory of ZALF for analyses of plant and soil extracts. We also thank Rivka Elbaum (The Hebrew University of Jerusalem) and Scott Nicholas Johnson (Western Sydney University) for their comments on an earlier version of the manuscript. Last but not least many thanks to three anonymous reviewers, whose critical comments improved the quality of our manuscript substantially.

Funding

DP was funded by the Deutsche Forschungsgemeinschaft (DFG) under grant PU 626/2–1.

Author information

Authors and Affiliations

Authors

Contributions

J.S. and M.S. designed the study and conducted the experiment. J.B. performed SEM–EDX analyses. S.P. and E.B. measured the condensation state of silica in the plant material. J.S. and D.P. wrote the manuscript with help of all other authors. All authors approved the final manuscript.

Corresponding author

Correspondence to Jörg Schaller.

Ethics declarations

Conflicts of interest

The authors declare that there are no conflicts of interest or competing interests.

Consent to participate and for publication

All authors consent to participate and for publication of the manuscript.

Additional information

Responsible Editor: Martin J. Hodson.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (DOCX 85 KB)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Schaller, J., Puppe, D., Busse, J. et al. Silicification patterns in wheat leaves related to ontogeny and soil silicon availability under field conditions. Plant Soil 477, 9–23 (2022). https://doi.org/10.1007/s11104-022-05385-6

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11104-022-05385-6

Keywords

Navigation