Skip to main content
Log in

Are fire resprouters more carbon limited than non-resprouters? Effects of elevated CO2 on biomass, storage and allocation of woody species

  • Published:
Plant Ecology Aims and scope Submit manuscript

Abstract

Resprouting ability is a key functional trait determining plant responses and vegetation dynamics after disturbances such as fire that shape most global biomes. It is likely that rising atmospheric CO2 concentrations will alter resource allocation patterns in plants which in turn will alter resprouting responses. In this study, we asked: (1) do resprouters have greater allocation to storage than non-resprouters?; (2) if so, do resprouters account for this negative carbon balance by having reduced growth?; and (3) do resprouters have a relatively weaker growth response compared to non-resprouters under elevated CO2 levels due to their increased allocation to storage? To address these questions, we grew congeneric species-pairs of shrubs common to south-eastern Australia with contrasting resprouting abilities under ambient and elevated CO2 levels. We found that resprouters in general allocated more resources to storage (root non-structural carbohydrates and biomass) and had less total biomass than non-resprouters. Under elevated CO2 levels both sprouting types increased biomass production, suggesting they were carbon limited. Surprisingly, the resprouters allocated this additional carbon to biomass rather than to storage. This suggests that although elevated CO2 levels may not affect resprouting ability directly in resprouters, it may enhance other aspects of persistence such as escapability and bud protection. Furthermore, non-resprouters may also benefit from the additional carbon by being able to set seed more quickly and increase seed production thus enhancing their recruitment after fire. Thus, the relative benefits of elevated CO2 levels on resprouters versus non-resprouters remain equivocal.

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

Similar content being viewed by others

References

  • Bell TL, Ojeda F (1999) Underground starch storage in Erica species of the Cape Floristic Region—differences between seeders and resprouters. New Phytol 144:143–152

    Article  CAS  Google Scholar 

  • Bell TL, Pate JS (1996) Growth and fire response of selected Epacridaceae of south-western Australia. Aust J Bot 44:509–526

    Article  Google Scholar 

  • Bond WJ (2008) What limits trees in C4 grasslands and savannas? Annu Rev Ecol Evol Syst 39:641–659

    Article  Google Scholar 

  • Bond WJ, Midgley GF (2000) A proposed CO2-controlled mechanism of woody plant invasion in grasslands and savannas. Glob Change Biol 6:865–869

    Article  Google Scholar 

  • Bond WJ, Midgley GF (2012) Carbon dioxide and the uneasy interactions of trees and savannah grasses. Philos Trans R Soc B 367:601–612

    Article  CAS  Google Scholar 

  • Bradley KL, Pregitzer KS (2007) Ecosystem assembly and terrestrial carbon balance under elevated CO2. Trends Ecol Evol 22:538–547

    Article  PubMed  Google Scholar 

  • Buitenwerf R, Bond WJ, Stevens N, Trollope WSW (2012) Increased tree densities in South African savannas: >50 years of data suggests CO2 as a driver. Glob Change Biol 18:675–684

    Article  Google Scholar 

  • Chew SJ, Bonser SP (2009) The evolution of growth rate, resource allocation and competitive ability in seeder and resprouter tree seedlings. Evol Ecol 23:723–735

    Article  Google Scholar 

  • Clarke PJ, Dorji K (2008) Are trade-offs in plant resprouting manifested in community seed banks? Ecology 89:1850–1858

    Article  PubMed  Google Scholar 

  • Clarke PJ, Knox KJE (2009) Trade-offs in resource allocation that favour resprouting affect the competitive ability of woody seedlings in grassy communities. J Ecol 97:1374–1382

    Article  Google Scholar 

  • Clarke PJ, Lawes MJ, Midgley JJ (2010) Resprouting as a key functional trait in woody plants: challenges to developing new organizing principles. New Phytol 188:651–654

    Article  PubMed  Google Scholar 

  • Clarke PJ et al (2013) Resprouting as a key functional trait: how buds, protection and resources drive persistence after fire. New Phytol 197:19–35

    Article  CAS  PubMed  Google Scholar 

  • Cruz A, Perez B, Moreno J (2003) Plant stored reserves do not drive resprouting of the lignotuberous shrub Erica australis. New Phytol 157:251–261

    Article  Google Scholar 

  • Davis MA, Reich PB, Knoll MJB, Dooley LEE, Hundtoft M, Attleson I (2007) Elevated atmospheric CO2: a nurse plant substitute for oak seedlings establishing in old fields. Glob Change Biol 13:2308–2316

    Article  Google Scholar 

  • Dietze MC, Clark JS (2008) Changing the gap dynamics paradigm: vegetative regeneration control on forest response to disturbance. Ecol Monogr 78:331–347

    Article  Google Scholar 

  • Dijkstra FA, Blumenthal D, Morgan JA, LeCain DR, Follett RF (2010) Elevated CO2 effects on semi-arid grassland plants in relation to water availability and competition. Funct Ecol 24:1152–1161

    Article  Google Scholar 

  • Fensham RJ, Fairfax RJ, Archer SR (2005) Rainfall, land use and woody vegetation cover change in semi-arid Australian savanna. J Ecol 93:596–606

    Article  Google Scholar 

  • Higgins SI, Scheiter S (2012) Atmospheric CO2 forces abrupt vegetation shifts locally, but not globally. Nature 488:209–212

    Article  CAS  PubMed  Google Scholar 

  • Hoffmann WA, Bazzaz FA, Chatterton NJ, Harrison PA, Jackson RB (2000) Elevated CO2 enhances resprouting of a tropical savanna tree. Oecologia 123:312–317

    Article  Google Scholar 

  • Hoffmann WA, Orthen B, Do Nascimento PKV (2003) Comparative fire ecology of tropical savanna and forest trees. Funct Ecol 17:720–726

    Article  Google Scholar 

  • IPCC (2011) Summary for policymakers. In: Field CB et al (eds) Managing the risks of extreme events and disasters to advance climate change adaptation. Cambridge University Press, Cambridge

    Google Scholar 

  • IPCC (2013) Climate change 2013: a physical science basis. In: Joussaume S, Penner J, Tangang F (eds) Working group I contribution to the IPCC fifth assessment report. Cambridge University Press, Cambridge

    Google Scholar 

  • Jablonski LM, Wang X, Curtis PS (2002) Plant reproduction under elevated CO2 conditions: a meta-analysis of reports on 79 crop and wild species. New Phytol 156:9–26

    Article  Google Scholar 

  • Kabeya D, Sakai S (2005) The relative importance of carbohydrate and nitrogen for the resprouting ability of Quercus crispula seedlings. Ann Bot 96:479–488

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Kgope BS, Bond WJ, Midgley GF (2010) Growth responses of African savanna trees implicate atmospheric [CO2] as a driver of past and current changes in savanna tree cover. Austral Ecol 35:451–463

    Article  Google Scholar 

  • Knox KJE, Clarke PJ (2005) Nutrient availability induces contrasting allocation and starch formation in resprouting and obligate seeding shrubs. Funct Ecol 19:690–698

    Article  Google Scholar 

  • Lawes M, Clarke P (2011) Ecology of plant resprouting: populations to community responses in fire-prone ecosystems. Plant Ecol 212:1937–1943

    Article  Google Scholar 

  • Lawes MJ, Adie H, Russell-Smith J, Murphy B, Midgley JJ (2011) How do small savanna trees avoid stem mortality by fire? The roles of stem diameter, height and bark thickness. Ecosphere 2:art42

    Article  Google Scholar 

  • Manea A, Leishman MR (2015) Competitive interactions between established grasses and woody plant seedlings under elevated CO2 levels are mediated by soil water availability. Oecologia 177:499–506

    Article  CAS  PubMed  Google Scholar 

  • Michaletz ST, Johnson EA, Tyree MT (2012) Moving beyond the cambium necrosis hypothesis of post-fire tree mortality: cavitation and deformation of xylem in forest fires. New Phytol 194:254–263

    Article  CAS  PubMed  Google Scholar 

  • Midgley JJ, Lawes MJ, Chamaillae-Jammes S (2010) Turner review no. 19—Savanna woody plant dynamics: the role of fire and herbivory, separately and synergistically. Aust J Bot 58:1–11

    Article  Google Scholar 

  • Midgley JJ, Kruger LM, Skelton R (2011) How do fires kill plants? The hydraulic death hypothesis and Cape Proteaceae “fire-resisters”. S Afr J Bot 77:381–386

    Article  Google Scholar 

  • Moreira B, Tormo J, Pausas JG (2005) To resprout or not to resprout: factors driving intraspecific variability in resprouting. Oikos 121:1577–1584

    Article  Google Scholar 

  • Morgan JA, LeCain DR, Mosier AR, Milchunas DG (2001) Elevated CO2 enhances water relations and productivity and affects gas exchange in C3 and C4 grasses of the Colorado shortgrass steppe. Glob Change Biol 7:451–466

    Article  Google Scholar 

  • Morgan JA, Milchunas DG, LeCain DR, West M, Mosier AR (2007) Carbon dioxide enrichment alters plant community structure and accelerates shrub growth in the shortgrass steppe. Proc Natl Acad Sci 104:14724–14729

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Myers JA, Kitajima K (2007) Carbohydrate storage enhances seedling shade and stress tolerance in a neotropical forest. J Ecol 95:383–395

    Article  CAS  Google Scholar 

  • Nano C, Clarke P (2011) Assembly rules for flammable arid vegetation: how does drought and fire influence patterns of resprouting and recruitment in arid and semi-arid Australia? Plant Ecol 212:2095–2110

    Article  Google Scholar 

  • Palacio S, Maestro M, Montserrat-Marti G (2007) Relationship between shoot-rooting and root-sprouting abilities and the carbohydrate and nitrogen reserves of Mediterranean dwarf shrubs. Ann Bot 100:865–874

  • Palacio S, Hoch G, Sala A, Körner C, Millard P (2014) Does carbon storage limit tree growth? New Phytol 201:1096–1100

    Article  CAS  PubMed  Google Scholar 

  • Pate JS, Froend RH, Bowen BJ, Hansen A, Kuo J (1990) Seedling growth and storage characteristics of seeder and resprouter species of mediterranean-type ecosystems of SW Australia. Ann Bot 65:585–601

    Google Scholar 

  • Paula S, Pausas JG (2006) Leaf traits and resprouting ability in the Mediterranean basin. Funct Ecol 20:941–947

    Article  Google Scholar 

  • Polley HW, Johnson HB, Derner JD (2003) Increasing CO2 from subambient to superambient concentrations alters species composition and increases above-ground biomass in a C3/C4 grassland. New Phytol 160:319–327

    Article  CAS  Google Scholar 

  • Poorter L, Kitajima K (2007) Carbohydrate storage and light requirements of tropical moist and dry forest tree species. Ecology 88:1000–1011

    Article  PubMed  Google Scholar 

  • Poorter L, Kitajima K, Mercado P, Chubina J, Melgar I, Prins HH (2010) Resprouting as a persistence strategy of tropical forest trees: relations with carbohydrate storage and shade tolerance. Ecology 91:2613–2627

    Article  PubMed  Google Scholar 

  • Prentice IC, Harrison SP, Bartlein PJ (2011) Global vegetation and terrestrial carbon cycle changes after the last ice age. New Phytol 189:988–998

    Article  CAS  PubMed  Google Scholar 

  • Shaw MR, Zavaleta ES, Chiariello NR, Cleland EE, Mooney HA, Field CB (2002) Grassland responses to global environmental changes suppressed by elevated CO2. Science 298:1987–1990

    Article  CAS  PubMed  Google Scholar 

  • Verdaguer D, Ojeda F (2002) Root starch storage and allocation patterns in seeder and resprouter seedlings of two Cape Erica (Ericaceae) species. Am J Bot 89:1189–1196

    Article  PubMed  Google Scholar 

  • Vesk P, Westoby M (2004) Sprouting ability across diverse disturbances and vegetation types worldwide. J Ecol 92:310–320

    Article  Google Scholar 

  • Wang X, Taub D (2010) Interactive effects of elevated carbon dioxide and environmental stresses on root mass fraction in plants: a meta-analytical synthesis using pairwise techniques. Oecologia 163:1–11

    Article  PubMed  Google Scholar 

  • Way D et al (2010) Greater seed production in elevated CO2 is not accompanied by reduced seed quality in Pinus taeda. Glob Change Biol 16:1046–1056

    Article  Google Scholar 

  • Wright A et al (2013) Complex facilitation and competition in a temperate grassland: loss of plant diversity and elevated CO2 have divergent and opposite effects on oak establishment. Oecologia 171:449–458

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

We gratefully acknowledge M. Masood (Department of Biological Sciences, Macquarie University) for assistance in the glasshouses and David Appleton (School of Agriculture and Food Sciences, University of Queensland) for conducting all soluble carbohydrates and starch analyses. This research was funded by a Macquarie University Safety Net grant. The experiments conducted complied with all current laws and regulations of Australia, where they were conducted.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Anthony Manea.

Additional information

Communicated by Prof. Michael Lawes, Prof. Ross Bradstock and Prof. David Keith.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary material 1 (PDF 626 kb)

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Clarke, P.J., Manea, A. & Leishman, M.R. Are fire resprouters more carbon limited than non-resprouters? Effects of elevated CO2 on biomass, storage and allocation of woody species. Plant Ecol 217, 763–771 (2016). https://doi.org/10.1007/s11258-015-0528-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11258-015-0528-y

Keywords

Navigation