Skip to main content
Log in

Effect of nutrient and light stress on the mortality and growth of young clonal and non-clonal herbs after biomass removal

  • Published:
Folia Geobotanica Aims and scope Submit manuscript

Abstract

Clonal herbs form belowground organs where they store reserves and bear regenerative buds. Based on these characteristics, clonal herbs may deal with disturbances better than non-clonal herbs, and clonality is seen as an adaptive strategy in disturbed habitats. The advantage of being clonal is likely to be enhanced in stressful conditions where larger belowground storage is beneficial. We conducted a greenhouse experiment to examine the ability of young plants to deal with biomass removal when exposed to light or nutrient stress or its combination. Using congeneric pairs of species, we evaluated the ability of clonal versus non-clonal groups to cope with biomass removal in terms of mortality, biomass productivity, specific leaf area and root-to-shoot ratio. We found that clonal and non-clonal herbs produce the same amount of biomass when injured and that nutrient and light stress does not alter biomass production. Both groups responded similarly to the biomass removal by increasing the specific leaf area and root-to-shoot ratio. Very young clonal herbs had higher mortality than non-clonal herbs of the same age. This fact suggests a higher survival probability in the non-clonal group, presumably originating from a greater population dependence on generative reproduction. We conclude that belowground organs in young plants, and thus bud banks and belowground storage, are not yet formed enough to give clonal herbs an advantage over non-clonal ones, and the advantage of clonality might manifest later in life when belowground organs are fully developed.

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

Similar content being viewed by others

References

  • Aarssen LW (2008) Death without sex – the ‘problem of the small’ and selection for reproductive economy in flowering plants. Evol Ecol 22:279–298

    Article  Google Scholar 

  • Batzer EE, Martina JP, Elgersma KJ, Goldberg DE (2017) Clonal plant allocation to daughter ramets is a simple function of parent size across species and nutrient levels. Pl Ecol 218:1299–1311

    Article  Google Scholar 

  • Benot ML, Morvan-Bertrand A, Mony C, Huet J, Sulmon C, Decau ML, Prud'homme MP, Bonis A (2019) Grazing intensity modulates carbohydrate storage pattern in five grass species from temperate grasslands. Acta Oecol 95:108–115

    Article  Google Scholar 

  • Casper BB, Jackson RB (1997) Plant competition underground. Annual Rev Ecol Syst 28:545–570

    Article  Google Scholar 

  • Chapin FS, Schulze E, Mooney HA (1990) The ecology and economics of storage in plants. Annual Rev Ecol Syst 21:423–447

    Article  Google Scholar 

  • Conner JK, Zangori LA (1998) Combined effects of water, nutrient, and UV-B stress on female fitness in Brassica (Brassicaceae). Amer J Bot 85:925–931

    Article  CAS  Google Scholar 

  • Day KJ, Hutchings MJ, John EA (2003) The effects of spatial pattern of nutrient supply on yield, structure and mortality in plant populations. J Ecol 91:541–553

    Article  Google Scholar 

  • Dong BC, Wang MZ, Liu RH, Luo FL, Li HL, Yu FH (2018) Direct and legacy effects of herbivory on growth and physiology of a clonal plant. Biol Invas 20:3631–3645

    Article  Google Scholar 

  • Drake PL, Mendham DS, White D, Ogden GN (2009) A comparison of growth, photosynthetic capacity and water stress in Eucalyptus globulus coppice regrowth and seedlings during early development. Tree Physiol 29:663–674

    Article  CAS  PubMed  Google Scholar 

  • Duchoslavová J, Jansa J (2018) The direction of carbon and nitrogen fluxes between ramets in Agrostis stolonifera changes during ontogeny under simulated competition for light. J Exp Bot 69:2149–2158

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  • Eriksson O, Jerling L (1990) Hierarchical selection and risk spreading in clonal plants. In van Groenendael J, de Kroon H (eds) Clonal growth in plants: regulation and function. SPB Academic Publishing, The Hague, pp. 79–94

  • Ferraro DO, Oesterheld M (2002) Effect of defoliation on grass growth. A quantitative review. Oikos 98:125–133

    Article  Google Scholar 

  • Ficken CD, Wright JP (2019) Nitrogen uptake and biomass resprouting show contrasting relationships with resource acquisitive and conservative plant traits. J Veg Sci 30:65–74

    Article  Google Scholar 

  • Fischer M, van Kleunen M (2002) On the evolution of clonal plant life histories. Ecol Evol 15:565–582

    Article  Google Scholar 

  • Grubb PJ, Lee WG, Kollmann J, Wilson JB (1996) Interaction of irradiance and soil nutrient supply on growth of seedlings of ten European tall-shrub species and Fagus sylvatica. J Ecol 84:827–840

    Article  Google Scholar 

  • He T, Lamont BB, Downes, KS (2011) Banksia born to burn. New Phytol 191:184–96

    Article  PubMed  Google Scholar 

  • Herben T, Šerá B, Klimešová J (2015) Clonal growth and sexual reproduction: tradeoffs and environmental constraints. Oikos 124:469–479

    Article  Google Scholar 

  • Hicks S, Turgtington R (2000) Compensatory growth of three herbaceous perennial species: the effects of clipping and nutrient availability. Canad J Bot 78:759–767

    Article  Google Scholar 

  • Hoffman MD, Gelman A (2014) The No-U-Turn sampler: adaptively setting path lengths in Hamiltonian Monte Carlo. J Machine Learning Res 4:1–30

    Google Scholar 

  • Janeček Š, Klimešová J (2014) Carbohydrate storage in meadow plants and its depletion after disturbance: Do roots and stem-derived organs differ in their roles? Oecologia 175:51–61

    Article  PubMed  Google Scholar 

  • Janovský Z, Herben T (2020) Reaching similar goals by different means - Differences in life-history strategies of clonal and non-clonal plants. Perspect Pl Ecol 44:125534

    Article  Google Scholar 

  • Keddy PA (2001) Competition. Kluwer, Dordrecht.

  • Klimešová J, Klimeš L (2008) Clonal growth diversity and bud banks of plants in the Czech flora: an evaluation using the CLO-PLA3 database. Preslia 80:255–275

    Google Scholar 

  • Klimešová J, Martínková J, Herben T (2018) Horizontal growth: An overlooked dimension in plant trait space. Perspect Plant Ecol 323:18–21. https://doi.org/10.1016/j.ppees.2018.02.002

  • Lapointe L, Bussieres J, Crete M, Ouellet JP (2010) Impact od growth form and carbohydrate reserves on tolerance to simulated deer herbivory and subsequent recovery in Liliaceae. Amer J Bot 97:913–924

    Article  Google Scholar 

  • Liu HD, Yu FH, He WM, Chu Y, Dong M (2007) Are clonal plants more tolerant to grazing than co-occurring non-clonal plants in inland dunes? Ecol Res 22:502–506

    Article  Google Scholar 

  • Martínková J, Klimeš A, Klimešová J (2020a) Young clonal and non-clonal herbs differ in growth strategy but not in aboveground biomass compensation after disturbance. Oecologia 193:925–935

    Article  PubMed  Google Scholar 

  • Martínková J, Klimeš A, Puy J, Klimešová J (2020b) Response of clonal versus non-clonal herbs to disturbance: different strategies revealed. Perspect Pl Ecol 44:125529

    Article  Google Scholar 

  • Maschinski J, Whitham TG (1989) The continuum of plant responses to herbivory: the influence of plant association, nutrient availability, and timing. Amer Nat 134:1–19

    Article  Google Scholar 

  • McKinley DC, Van Auken OV (2005) Influence of interacting factors on the growth and mortality of Juniperus seedlings. Amer Midl Naturalist 154:320–330

    Article  Google Scholar 

  • Moore NA, Camac JS, Morgan JW (2018) Effects of drought and fire on resprouting capacity of 52 temperate Australian perennial native grasses. New Phytol 221:1424–1433

    Article  PubMed  Google Scholar 

  • Ott JP, Klimešová J, Hartnett DC (2019) The ecology and significance of below-ground bud banks in plants. Ann Bot (London) 123:1099–1118

    Article  Google Scholar 

  • Ottaviani G, Lubbe FC, Lepš J, Lisner A, Martínková J, Mudrák O, Klimešová J (2021) Strong impact of management regimes on rhizome biomass across Central European temperate grasslands. Ecol Applic 31:e02317

    Article  Google Scholar 

  • Paula S, Ojeda F (2009) Belowground starch consumption after recurrent severe disturbance in three resprouter species of the genus Erica. Botany 87:253–259

    Article  Google Scholar 

  • Pennings SC, Callaway RM (2000) The advantages of clonal integration under different ecological conditions: a community-wide test. Ecology 81:709–716

    Article  Google Scholar 

  • Pérez-Harguindeguy N, Díaz S, Garnier E, Lavorel S, Poorter H, Jaureguiberry P, ... Cornelissen JHC (2013) New handbook for standardised measurement of plant functional traits worldwide. Aus J Bot 61:167–234. https://doi.org/10.1071/BT12225_CO

  • R Core Team (2016) R: a language and environment for statistical computing, R Foundation for Statistical Computing, Vienna. Available at https://www.r-project.org

  • Reich PB (2014) The world-wide ‘fast–slow’ plant economics spectrum: a traits manifesto. J Ecol 102:275–301

    Article  Google Scholar 

  • Šmilauerová M, Šmilauer P (2007) What youngsters say about adults: Seedling roots reflect clonal traits of adult plants. J Ecol 95:406–413

    Article  Google Scholar 

  • Stan Development Team (2018) RStan: the R interface to Stan. R package. Retrieved from http://mc-stan.org/

  • Thalmann M, Santelia D (2017) Starch as a determinant of plant fitness under abiotic stress. New Phytol 214:943–951

    Article  CAS  PubMed  Google Scholar 

  • Van Der Heyden F, Stock WD (1996) Regrowth of a semiarid shrub following simulated browsing: the role of reserve carbon. Funct Ecol 10:647–653

    Article  Google Scholar 

  • Wan JZ, Wang CJ, Yu FH (2019) Large-scale environmental niche variation between clonal and non-clonal plant species: roles of clonal growth organs and ecoregions. Sci Total Environm 652:1071–1076

    Article  CAS  Google Scholar 

  • Weiser M, Koubek T, Herben T (2016). Root foraging performance and life-history traits. Frontiers Pl Sci 7:779

    Google Scholar 

  • Wilson SD, Tilman D (1993) Plant competition and resource availability in response to disturbance and fertilization. Ecology 74:599–611

    Article  Google Scholar 

  • Wise MJ, Abrahamson WG (2005) Beyond the compensatory continuum: environmental resource levels and plant tolerance of herbivory. Oikos 109:417–428

    Article  Google Scholar 

  • Wise MJ, Abrahamson WG (2007) Effects of resource availability on tolerance of herbivory: a review and assessment of three opposing models. Amer Naturalist 169:443–454

    Article  Google Scholar 

  • Wright IJ, Reich PB, Westoby M, Ackerly DD, Baruch Z, Bonger F, Cavender-Bares J, Chapin T, Cornelissen JHC, Diemer M, Flexas J, Garnier E, Groom PK, Gulias J, Hikosaka K, Lamon BB, Lee T, Lee W, Lus C, Midgle JJ, Nava ML, Niinemets Ü, Oleksyn J, Osada N, Poorter H, Poot P, Prior L, Pyanko VI, Roumet C, Thoma SC, Tjoelker MG, Veneklaas EJ, Villar R (2004) The worldwide leaf economic spectrum. Nature 428:821–827

    Article  CAS  PubMed  Google Scholar 

  • Zhu C, Chen Y, Li W et al (2014) Effect of herbivory on the growth and photosynthesis of replanted Calligonum caputmedusaesaplings in an infertile arid desert. Plant Ecol 215:155–167. https://doi.org/10.1007/s11258-013-0286-7

Download references

Acknowledgements

The work was supported by the Czech Science Foundation (grant No. 19-13231S) and by the long-term research project of the Czech Academy of Sciences RVO 67985939. We would like to thank Tomáš Herben for valuable methodological and statistical advice.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jana Martínková.

Additional information

Publisher’s Note

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

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Martínková, J., Klimeš, A. & Klimešová, J. Effect of nutrient and light stress on the mortality and growth of young clonal and non-clonal herbs after biomass removal. Folia Geobot 56, 99–108 (2021). https://doi.org/10.1007/s12224-021-09395-7

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12224-021-09395-7

Keywords

Navigation