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Differences in the compensatory growth of two co-occurring grass species in relation to water availability

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Abstract

We compared the potential for compensatory growth of two grass species from the Mongolian steppe that differ in their ability to persist under grazing: the rhizomatous Leymus chinensis and the caespitose Stipa krylovii, and investigated how this ability might be affected by drought. Plants were grown in a greenhouse under wet and dry conditions and subjected to a clipping treatment (biweekly removal of 75–90% of the aerial mass). Leymus exhibited a much stronger compensatory growth after clipping than Stipa. Leymus showed a significant increase in its relative growth rate (RGR) after clipping, while for Stipa RGR was negatively affected. Clipped Leymus plants maintained leaf productivity levels that were similar to undamaged individuals, while leaf-productivity in clipped Stipa dropped to less than half of that of the controls. In Leymus, there was less compensatory growth under dry than under wet conditions, while in Stipa the compensation was increased under drought. This difference probably reflects the fact that Stipa is more drought-tolerant than Leymus. The greater compensatory growth of Leymus compared to Stipa mainly resulted from a greater stimulation of its net assimilation rate (NAR), and its greater capacity to store and reallocate carbohydrates by clipping. The greater increase in NAR was probably the result of a stronger reduction in self-shading, because Leymus shoots were much denser than those of Stipa, which resulted in a higher increase in light penetration to remaining leaves after clipping. The results of this study suggest that the greater ability of Leymus to persist under grazing is the result of its larger capacity for compensatory growth.

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References

  • Anten NPR, Ackerly DD (2001a) Canopy-level photosynthetic compensation after defoliation in a tropical understorey palm. Funct Ecol 15:252–262

    Article  Google Scholar 

  • Anten NPR, Ackerly DD (2001b) A new method of growth analysis for plants that experience periodic losses of leaf mass. Funct Ecol 15:804–811

    Article  Google Scholar 

  • Anten NPR, Martinez-Ramos M, Ackerly DD (2003) Defoliation and growth in an understory palm: quantifying the contributions of compensatory responses. Ecology 84:2905–2918

    Article  Google Scholar 

  • Archer S, Detling JK (1986) Evaluation of potential herbivore mediation of plant water status in a North American mixed-grass prairie. Oikos 47:287–291

    Article  Google Scholar 

  • Belsky AJ, Carson WP, Jensen CL, Fox GA (1993) Overcompensation by plants: herbivore optimization or red herring? Evol Ecol 7:109–121

    Article  Google Scholar 

  • Caldwell MM, Richards JH, Johnson DA, Nowak RS, Dzurec RS (1981) Coping with herbivory: photosynthetic capacity and resource allocation in two semiarid Agropyron bunchgrasses. Oecologia 50:14–24

    Article  Google Scholar 

  • Chapin FS III, Schulze ED, Mooney HA (1990) The ecology and economics of storage in plants. Ann Rev Ecol Syst 21:423–427

    Article  Google Scholar 

  • Coughenour MB, Detling JK, Bamberg IE, Mugambi MM (1990) Production and nitrogen responses of the African dwarf shrub Indigofera spinosa to defoliation and water limitation. Oecologia 83:546–552

    Article  Google Scholar 

  • Davidson JL, Milthorpe FL (1966) The effect of defoliation on the carbon balance in Dactylis glomerata. Ann Bot 30:185–198

    CAS  Google Scholar 

  • Day TA, Detling JK (1994) Water relations of Agropyron smithii and Bouteloua gracilis and community evapotranspiration following long-term grazing by Prairie dogs. Am Mid Nat 132:381–392

    Article  Google Scholar 

  • Evans JR (1989) Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia 78:9–19

    Article  Google Scholar 

  • Fernandez-Gimenez M, Allen-Diaz B (2001) Vegetation change along gradients from water sources in three grazed Mongolian ecosystems. Plant Ecol 157:101–118

    Article  Google Scholar 

  • Gold WG, Caldwell MM (1990) The effects of the spatial pattern of defoliation on regrowth of a tussock grass III. Photosynthesis, canopy structure and light interception. Oecologia 82:12–17

    Article  Google Scholar 

  • Gunin PD, Vostokova EA, Dorofeyuk PE, Tarasov PE, Black CC (1999) Analysis of present-day vegetation dynamics. In: Vegetation dynamics of Mongolia. Geobotany 26:131–164

  • Hilbert DW, Swift DM, Detling JK, Dyer MI (1981) Relative growth rates and the grazing optimization hypothesis. Oecologia 51:14–18

    Article  Google Scholar 

  • Hilbig W (1995) The vegetation of Mongolia. SPB Academic Publishers, Amsterdam

    Google Scholar 

  • Kobe RK (1997) Carbohydrate allocation to storage as a basis of interspecific variation in sapling survivorship and growth. Oikos 80:226–233

    Article  Google Scholar 

  • Mack RN, Thompson JN (1982) Evolution in steppe with few large, hooved mammals. Am Nat 119:757–777

    Article  Google Scholar 

  • McNaughton SJ (1983) Compensatory plant growth as a response to herbivory. Oikos 40:329–336

    Article  Google Scholar 

  • Milchunas DG, Sala OE, Lauenroth WK (1988) A generalized model of the effects of grazing by large herbivores on grassland community structure. Am Nat 132:87–106

    Article  Google Scholar 

  • McPherson K, Williams K (1998) The role of carbohydrate reserves in the growth, resilience, and persistence of cabbage palm seedlings (Sabal palmetto). Oecologia 117:460–468

    Article  Google Scholar 

  • Nowak RS, Caldwell MM (1984) A test of compensatory photosynthesis in the field: implications for herbivory tolerance. Oecologia 61:311–318

    Article  Google Scholar 

  • Oesterheld M (1992) Effect of defoliation intensity on aboveground and belowground relative growth rates. Oecologia 92:313–316

    Article  Google Scholar 

  • Oesterheld M, McNaughton SJ (1988) Intraspecific variation in the response of Themeda triandra to defoliation: the effect of time of recovery and growth rates on compensatory growth. Oecologia 77:181–186

    Article  Google Scholar 

  • Oesterheld M, McNaughton SJ (1991) Effect of stress and time for recovery on the amount of compensatory growth after grazing. Oecologia 85:305–313

    Article  Google Scholar 

  • Richards JH, Caldwell MM (1985) Soluble carbohydrates, concurrent photosynthesis and efficiency in regrowth following defoliation: a field study with Agropyron species. J Appl Ecol 22:907–920

    Article  Google Scholar 

  • Senock RS, Sisson WB, Donart GB (1991) Compensatory photosynthesis of sporobolus flexuosus (Thurb.) Rydb. following simulated herbivory in the northern Chichuahuan desert. Bot Gaz 152:275–281

    Article  Google Scholar 

  • Stowe KA, Marquis RJ, Hochwender CG, Simms EL (2000) The evolutionary ecology of tolerance to consumer damage. Ann Rev Ecol Syst 31:565–595

    Article  Google Scholar 

  • Takhi reintroduction centre (1998) Inventories and monitoring at Hustain Nuruu National Park. Mongolian association for conservation of nature and the environment. Internal report

  • Trlica MJ, Cook CW (1971) Defoliation effects on carbohydrate reserves of desert species. J Range Manage 24:418–425

    Article  CAS  Google Scholar 

  • Wallis de Vries MF, Manibazar N, Dugerlham S (1996) The vegetation of the forest-steppe region of Hustain Nuruu, Mongolia. Vegetatio 122:111–127

    Article  Google Scholar 

  • Werger MJA, Hirose T, During HJ, Heil GW, Hikosaka K, Ito T, Nachinshonhor UG, Nagamatsu D, Shibasaki K, Takatsuki S, Van Rheenen JW, Anten NPR (2002) Light partitioning among species and species replacement in early successional grasslands. J Veg Sci 13:615–626

    Article  Google Scholar 

  • Xiao X, Wang Y, Jiang S, Ojima DS, Bonham CD (1995) Interannual variation in the climate and above-ground biomass of Leymus chinense steppe and Stipa grandis steppe in the Xilin river basin, Inner Mongolia, China. J Arid Environ 31:283–299

    Article  Google Scholar 

  • Xie Y, Wittig R (2003) Growth parameters of characteristic species of Stipa steppes in Norhern China as indicators of the grazing intensity. J Appl Bot 77:68–74

    Google Scholar 

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Acknowledgements

We thank Sonja Huggers, Sander van Hal, Henri Noordman, Amparo Carrillo-Gavilán and Betty Verduyn for their technical assistance with the greenhouse experiment. We also thank Marinus Werger and Heinjo During for comments on the manuscript and the staff of Hustai National Park for logistical support. MAvS acknowledges financial support by the Foundation for the Preservation and Protection of the Przewalski Horse (FPPPH) and the Schure-Beijerinck-Popping Fonds. Our experiments comply with the current laws in The Netherlands.

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Correspondence to Niels P.R. Anten.

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Communicated by Christian Koerner

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van Staalduinen, M.A., Anten, N.P. Differences in the compensatory growth of two co-occurring grass species in relation to water availability. Oecologia 146, 190–199 (2005). https://doi.org/10.1007/s00442-005-0225-y

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