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RESEARCH ARTICLE

Summer warming effects on biomass production and clonal growth of Leymus chinensis

Jun-Feng Wang A B , Song Gao A B , Ji-Xiang Lin A B , Yong-Guang Mu C and Chun-Sheng Mu A B D
+ Author Affiliations
- Author Affiliations

A Key Laboratory of Vegetation Ecology, Ministry of Education, Institute of Grassland Science, Northeast Normal University, Changchun 130024, People’s Republic of China.

B School of Life Sciences, Northeast Normal University, Changchun 130024, People’s Republic of China.

C School of Life Sciences, Jilin Normal University, Siping 136000, People’s Republic of China.

D Corresponding author. Email: mucs821@gmail.com

Crop and Pasture Science 61(8) 670-676 https://doi.org/10.1071/CP10012
Submitted: 13 January 2010  Accepted: 28 June 2010   Published: 13 August 2010

Abstract

Understanding how the biomass production and clone growth of perennial grasses respond to summer warming is crucial for understanding how grassland productivity responds to global warming. Here, we experimentally investigated the effects of summer warming on the biomass production and clonal growth of potted Leymus chinensis in a phytotron. Summer warming significantly decreased the biomass of both parent and daughter shoots, slightly increased the belowground biomass, and lead to a significant increase in root : shoot ratio. Warming significantly increased the total belowground bud number and decreased the daughter shoot number. Importantly, the proportions of each type of bud changed; vertical apical rhizome buds decreased, while horizontal rhizome buds increased in number. The change in proportions of each type of bud is closely related to the decrease in daughter shoot number, rhizome number and length, as well as the decrease in aboveground biomass and increase in belowground biomass. These results indicate that, as a rhizomatous, perennial grass, L. chinensis adopts a selective growth strategy that reduces the energy allocated to aboveground growth and emphasises the development of belowground organs. The implication is that continued summer warming, will further reduce the aboveground biomass production of temperate grasslands dominated by rhizomatous, perennial grasses. Inevitably, species that depend on these grasses for forage will suffer should global climate warming continue.

Additional keywords: biomass production, bud bank, clone growth, Leymus chinensis, summer warming.


Acknowledgments

The research was funded by National Natural Science Foundation of China (30471231). We thank M. S. Hui Yu and M. S. Guang Yang for their help in the laboratory.


References


Aber JD , Melillo JM (1991) ‘Terrestrial ecosystems.’ (Saunders College Publishing: Philadelphia, PA)

Alward RD, Detling JK, Milchunas DG (1999) Grassland vegetation changes and nocturnal global warming. Science 283, 229–231.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Baldocchi DD, Falge E, Gu L, Olson R, Hollinger D, Running S, Anthoni P, Bernhofer C, Davis K, Evans R, Fuentes J, Goldstein A, Katul G, Law B, Lee X, Malhi Y, Meyers T, Munger W, Oechel W, Paw U KT, Pilegaard K, Schmid HP, Valentini R, Verma S, Vesala T, Wilson K, Wofsy S (2001) Fluxnet: a new tool to study the temporal and spatial variability of the ecosystem-scale carbon dioxide, water vapor, and energy flux densities. Bulletin of the American Meteorological Society 82, 2415–2434.
Crossref | GoogleScholarGoogle Scholar | open url image1

Bao SD (2000) ‘Soil-agricultural chemistry analysis methods.’ pp. 42–58. (China Agriculture Press: Beijing)

Benson EJ, Hartnett DC (2006) The role of seed and vegetative reproduction in plant recruitment and demography in tallgrass prairie. Plant Ecology 187, 163–178.
Crossref | GoogleScholarGoogle Scholar | open url image1

Benson EJ, Hartnett DC, Mann KH (2004) Belowground bud banks and meristem limitation in tallgrass prairie plant populations. American Journal of Botany 91, 416–421.
Crossref | GoogleScholarGoogle Scholar | open url image1

Bond WJ, Midgley JJ (2001) Ecology of sprouting in woody plants: the persistence niche. Trends in Ecology & Evolution 16, 45–51.
Crossref | GoogleScholarGoogle Scholar | open url image1

Chaves MM, Pereira JS, Maroco J, Rodrigues ML, Ricardo CPP, Osorio ML, Carvalho I, Faria T, Pinheiro C (2002) How plants cope with water stress in the field? Photosynthesis and growth. Annals of Botany 89, 907–916.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Chen MJ , Jia SX (2002) ‘Fodder plants of China.’ pp. 194–198. (Agriculture Press of China: Beijing)

Dalgleish HJ, Hartnett DC (2006) Below-ground bud banks increase along a precipitation gradient of the North American Great Plains: a test of the meristem limitation hypothesis. New Phytologist 171, 81–89.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

De Boeck HJ, Lemmens CMHM, Gielen B, Malchair S, Carnol M, Merckx R, Van den Berge J, Ceulemans R, Nijs I (2007) Biomass production in experimental grasslands of different species richness during three years of climate warming. Biogeosciences Discussions 4, 4605–4629.
Crossref | GoogleScholarGoogle Scholar | open url image1

De Kroon H , Bobbink R (1997) Clonal plant dominance under elevated nitrogen deposition, with special reference to Brachypodium pinnatum in chalk grassland. In ‘The ecology and evolution of clonal plants’. (Eds H De Kroon, J Van Groenendael) pp. 359–379. (Backhuys Publishers: Leiden)

Gao Q, Yu M, Zhang XS, Guan F (1997) Dynamic modeling of northeast China transect responses to global change – a regional vegetation model driven by remote sensing information. Acta Botanica Sinica 39, 800–810. open url image1

Harper JL (1977) ‘Population biology of plants.’ (Academic Press: London)

Houghton JT , Ding Y , Griggs DJ , Noguer M , van der Linden PJ , Dai X , Maskell K , Johnson CA (2001) ‘Climate Change 2001: the scientific basis.’ (Cambridge University Press: New York)

IPCC (2007) ‘IPCC WGI Fourth Assessment Report. Climatic Change: the physical science basis.’ (Intergovernmental Panel on Climate Change: Geneva)

Knapp AK, Smith MD (2001) Variation among biomes in temporal dynamics of aboveground primary production. Science 291, 481–484.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Lamber H , Chapin FS III , Pons TL (1998) ‘Plant physiological ecology.’ (Springer: New York)

Loik ME, Redar SP, Harte J (2000) Photosynthetic response to a climate-warming manipulation for contrasting meadow species in the Rocky Mountains, Colorado, USA. Functional Ecology 14, 166–175.
Crossref | GoogleScholarGoogle Scholar | open url image1

McCallum MH, Kirkegaard JA, Green TW, Creswell HP, Davies SL, Angus JF, Peoples MB (2004) Improved subsoil macroporosity following perennial pastures. Australian Journal of Agricultural Research 44, 299–307. open url image1

Niu SL, Wu MY, Han Y, Xia JY, Li LH, Wan SQ (2008) Water-mediated responses of ecosystem carbon fluxes to climatic change in a temperate steppe. New Phytologist 177, 209–219.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Pedersen JK (2009) Above and belowground phenology in a heathland during future climate change. In ‘Climate Change: Global Risks, Challenges and Decisions’. IOP Conference Series, IOP Publishing. Earth and Environmental Science 312011. doi:10.1088/1755-1307/6/1/312011

Peltzer DA (2002) Does clonal integration improve competitive ability? A test using aspen (Populus termuloides [Salicaceae]). Invasion into prairie. American Journal of Botany 89, 494–499.
Crossref | GoogleScholarGoogle Scholar | open url image1

Piao SL, Fang JY, Chen AP (2003) Seasonal dynamics of terrestrial net primary production in response to climatic changes in China. Acta Botanica Sinica 45, 269–275. open url image1

Pitelka LF , Ashmun JW (1985) Physiology and integration of ramets in clonal plants. In ‘Population biology and evolution of clonal organisms’. (Eds JBC Jackson, LW Buss, RE Cook) pp. 399–436. (Yale University Press: New Haven, CT)

Post E, Pedersen C (2008) Opposing plant community responses to warming with and without herbivores. Proceedings of the National Academy of Sciences of the United States of America 105, 12 353–12 358.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Post E, Pedersen C, Wilmers CC, Forchhammer MC (2008) Phenological sequences reveal aggregate life history response to climate. Ecology 89, 363–370.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Rogers WE, Hartnett DC (2001) Temporal vegetation dynamics and recolonization mechanisms on different-sized soil disturbances in tallgrass prairie. American Journal of Botany 88, 1634–1642.
Crossref | GoogleScholarGoogle Scholar | open url image1

Rustad LE, Campbell JL, Marion GM, Norby RJ, Mitchell MJ, Hartley AE, Cornelissen JHC, Gurevitch J, GCTE-News (2001) A meta-analysis of the response of soil respiration, net nitrogen mineralization, and aboveground plant growth to experimental ecosystem warming. Oecologia 126, 543–562.
Crossref | GoogleScholarGoogle Scholar | open url image1

Rustad LE , Norby RJ (2002) Temperature increase: effects on terrestrial ecosystems. In ‘The Earth System: Biological and Ecological Dimensions of Global Environmental Change. Vol. 2. Encyclopedia of Global Environmental Change’. (Eds HA Mooney, JG Canadell) pp. 575–581. (John Wiley and Sons: Chichester, UK)

Ryan MG (1991) Effects of climate change on plant respiration. Ecological Applications 1, 157–167.
Crossref | GoogleScholarGoogle Scholar | open url image1

Shapiro SS, Wilk MB (1965) An analysis of variance test for normality. Biometrika 52, 591–599. open url image1

Shaver GR, Canadell J, Chapin FS, Gurevitch J, Henry JHG, Ineson P, Jonasson S, Melillo J, Pitelka L, Rustad L (2000) Global warming and terrestrial ecosystems: a conceptual framework for analysis. Bioscience 50, 871–882.
Crossref | GoogleScholarGoogle Scholar | open url image1

Vegis A (1964) Dormancy in higher plants. Annual Review of Plant Physiology 15, 185–224.
Crossref | GoogleScholarGoogle Scholar | open url image1

Vesk PA, Westoby M (2004) Funding the bud bank: a review of the costs of buds. Oikos 106, 200–208.
Crossref | GoogleScholarGoogle Scholar | open url image1

Wan SQ, Hui DF, Wallace LL, Luo YQ (2005) Direct and indirect warming effects on ecosystem carbon processes in a tallgrass prairie. Global Biogeochemical Cycles 19, GB2014.
Crossref | GoogleScholarGoogle Scholar | open url image1

Wan SQ, Xia JY, Liu WX, Niu SL (2009) Photosynthetic overcompensation under nocturnal warming enhances grassland carbon sequestration. Ecology 90, 2700–2710.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Wang JF, Xie JF, Zhang YT, Gao S, Zhang JT, Mu CS (2010) Methods to improve seed yield of Leymus chinensis based on nitrogen application and precipitation analysis. Agronomy Journal 102, 277–281.
Crossref | GoogleScholarGoogle Scholar | open url image1

Wilmking M, Juday GP, Barber VA, Zald HSJ (2004) Recent climate warming forces contrasting growth responses of white spruce at treeline in Alaska through temperature thresholds. Global Change Biology 10, 1724–1736.
Crossref | GoogleScholarGoogle Scholar | open url image1

Xia JY, Niu SL, Wan SQ (2009) Response of ecosystem carbon exchange to warming and nitrogen addition during two hydrologically contrasting growing seasons in a temperate steppe. Global Change Biology 15, 1544–1556.
Crossref | GoogleScholarGoogle Scholar | open url image1

Zhang JT, Mu CS, Wang DL, Wang JF, Chen GX (2009) Shoot population recruitment from a bud bank, over two seasons of undisturbed growth of Leymus chinensis. Canadian Journal of Botany 87, 1242–1249.
Crossref | GoogleScholarGoogle Scholar | open url image1