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Within-twig biomass allocation in subtropical evergreen broad-leaved species along an altitudinal gradient: allometric scaling analysis

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Abstract

We studied the effects of twig size and altitude on biomass allocation within plant twigs (terminal branches of current-year shoots), to determine whether species with large twigs/leaves or living at low altitude allocate a higher proportion of biomass to laminas than their counterparts with small twigs/leaves or living at high altitude. Stem mass, lamina mass and area, and petiole mass were measured for terminal branches of current-year shoots in 80 subtropical evergreen broad-leaved species belonging to 38 genera from 24 families along an altitudinal gradient of Mt. Emei, Southwest China. The scaling relationships between the biomass allocations of within-twig components were determined using model type II regression method. Isometric relationships were found between leaf mass and twig mass and between lamina mass and twig mass, suggesting that the biomass allocation to either leaves or laminas was independent of twig mass. Petiole mass disproportionally increased with both lamina mass and twig mass, indicating the importance of leaf petioles to the within-twig biomass allocation. These cross-species correlations were consistent with those among evolutionary divergences. In addition, species at low altitude tended to have a greater leaf and lamina mass but a smaller stem mass at a given twig mass than at middle and high altitudes. This is possibly due to the high requirement in physical support and the low efficiency of eco-physiological transport for the species living at high altitude. In general, within-twig biomass allocation pattern was not significantly affected by twig size but was greatly modulated by altitude.

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References

  • Bonser SP, Aarssen LW (1996) Meristem allocation: a new classification theory for adaptive strategies in herbaceous species. Oikos 77:347–352. doi:10.2307/3546076

    Article  Google Scholar 

  • Bazzaz FA, Grace J (1997) Plant resource allocation. Academic Press, London

    Google Scholar 

  • Brouat C, Gibernau M, Amsellem L, McKey D (1998) Corner’s rules revisited: ontogenetic and interspecific patterns in leaf-stem allometry. New Phytol 139:459–470. doi:10.1046/j.1469-8137.1998.00209.x

    Article  Google Scholar 

  • Chapin FSIII, Schulze ED, Mooney HA (1990) The ecology and economics of storage in plants. Annu Rev Ecol Syst 21:423–447. doi:10.1146/annurev.es.21.110190.002231

    Article  Google Scholar 

  • Corner EJH (1949) The durian theory or the origin of the modern tree. Ann Bot (Lond) 13:367–414

    Google Scholar 

  • Davis SD, Sperry JS, Hacke UG (1999) The relationship between xylem conduit diameter and cavitation caused by freezing. Am J Bot 86:1367–1372. doi:10.2307/2656919

    Article  PubMed  Google Scholar 

  • Editor Committee of the Chinese Academy of Sciences for Flora of China (ECCAS) (1974–1999) Flora of China (in Chinese). Science Press, Beijing

  • Enquist BJ, West GB, Charnov EL, Brown JH (1999) Allometric scaling of production and life-history variation in vascular plants. Nature 401:907–911. doi:10.1038/44819

    Article  CAS  Google Scholar 

  • Evans GC (1972) The quantitative analysis of plant growth. Blackwell, London

    Google Scholar 

  • Falster DS, Warton DI, Wright IJ (2006) User’s guide to SMATR: Standardised major axis tests and routines Version 2.0, Copyright 2006. http://www.bio.mq.edu.au/ecology/SMATR/ 13 Nov 2006

  • Gebauer RLE, Reynolds JF, Strain BR (1996) Allometric relations and growth in Pinus taeda: the effect of elevated CO2 and changing N availability. New Phytol 134:85–93. doi:10.1111/j.1469-8137.1996.tb01148.x

    Article  Google Scholar 

  • Givnish T (1984) Leaf and canopy adaptations in tropical forests. In: Medina E, Mooney HA, Vázquez-Yánes C (eds) Physiological ecology of plants of the wet tropics. Dr. W. Junk Publishers, Boston, pp 51–84

    Google Scholar 

  • Harper JL (1977) Population biology of plants. Academic Press, New York

    Google Scholar 

  • Li G, Yang D, Sun S (2008) Allometric relationships between lamina area, lamina mass and petiole mass of 93 temperate woody species vary with leaf habit, leaf form and altitude. Funct Ecol 22:557–564. doi:10.1111/j.1365-2435.2008.01407.x

    Article  Google Scholar 

  • Martins EP (2004) COMPARE, version 4.6b. Computer programs for the statistical analysis of comparative data. Distributed by the author at http://compare.bio.indiana.edu/. Department of Biology, Indiana University, Bloomington IN, USA

  • Mediavilla S, Escudero A (2003) Leaf life span differs from retention time of biomass and nutrients in the crowns of evergreen species. Funct Ecol 17:541–548. doi:10.1046/j.1365-2435.2003.00766.x

    Article  Google Scholar 

  • McConnaughay KDM, Coleman JS (1999) Biomass allocation in plants: ontogeny or optimality? A test along three resource gradients. Ecology 80:2581–2593

    Article  Google Scholar 

  • Niinemets Ü (1997) Distribution patterns of foliar carbon and nitrogen as affected by tree dimensions and relative light conditions in the canopy of Picea abies. Trees (Berl) 11:144–154

    Google Scholar 

  • Niinemets Ü (1998) Are compound-leaved woody species inherently shade-intolerant? An analysis of species ecological requirements and foliar support costs. Plant Ecol 134:1–11. doi:10.1023/A:1009773704558

    Article  Google Scholar 

  • Niinemets Ü, Kull O (1999) Biomass investment in leaf lamina versus lamina support in relation to growth irradiance and leaf size in temperate deciduous trees. Tree Physiol 19:349–358

    PubMed  Google Scholar 

  • Niinemets Ü, Portsmuth A, Tobias M (2006) Leaf size modifies support biomass distribution among stems, petioles and mid-ribs in temperate plants. New Phytol 171:91–104. doi:10.1111/j.1469-8137.2006.01741.x

    Article  PubMed  Google Scholar 

  • Niinemets Ü, Portsmuth A, Tobias M (2007a) Leaf shape and venation pattern alter the support investments within leaf lamina in temperate species: a neglected source of leaf physiological differentiation? Funct Ecol 21:28–40. doi:10.1111/j.1365-2435.2006.01221.x

    Article  Google Scholar 

  • Niinemets Ü, Portsmuth A, Tena D, Tobias M, Matesanz S, Valladares F (2007b) Do we underestimate the importance of leaf size in plant economics? Disproportional scaling of support costs within the spectrum of leaf physiognomy. Ann Bot (Lond) 100:283–303. doi:10.1093/aob/mcm107

    Article  CAS  Google Scholar 

  • Niklas KJ (1992) Petiole mechanics, light interception by lamina, and ‘economy in design’. Oecologia 90:518–526. doi:10.1007/BF01875445

    Article  Google Scholar 

  • Niklas KJ (1993) Testing ‘economy in design’ in plants: are the petioles and rachises of leaves ‘designed’ according to the principle of uniform strength? Ann Bot (Lond) 71:33–41. doi:10.1006/anbo.1993.1004

    Article  Google Scholar 

  • Niklas KJ (1999) Research review: a mechanical perspective on foliage leaf form and function. New Phytol 143:19–31. doi:10.1046/j.1469-8137.1999.00441.x

    Article  Google Scholar 

  • Niklas KJ, Enquist BJ (2002) On the vegetative biomass partitioning of seed plant leaves, stems, and roots. Am Nat 159:482–497. doi:10.1086/339459

    Article  PubMed  Google Scholar 

  • Normand F, Bissery C, Damour G, Lauri PE (2008) Hydraulic and mechanical stem properties affect leaf-stem allometry in mango cultivars. New Phytol 178:590–602. doi:10.1111/j.1469-8137.2008.02380.x

    Article  PubMed  CAS  Google Scholar 

  • Osada N (2006) Crown development in a pioneer tree, Rhus trichocarpa, in relation to the structure and growth of individual branches. New Phytol 172:667–678. doi:10.1111/j.1469-8137.2006.01857.x

    Article  PubMed  Google Scholar 

  • Pearcy RW, Muraoka H, Valladares F (2005) Crown architecture in sun and shade environments: assessing function and trade-offs with a three-dimensional simulation model. New Phytol 166:791–800. doi:10.1111/j.1469-8137.2005.01328.x

    Article  PubMed  Google Scholar 

  • Pickup M, Westoby M, Basden A (2005) Dry mass costs of deploying leaf area in relation to leaf size. Funct Ecol 19:88–97. doi:10.1111/j.0269-8463.2005.00927.x

    Article  Google Scholar 

  • Pitman ETG (1939) A note on normal correlation. Biometrika 31:9–12

    Google Scholar 

  • Preston KA, Ackerly DD (2003) Hydraulic architecture and the evolution of shoot allometry in contrasting climates. Am J Bot 90:1502–1512. doi:10.3732/ajb.90.10.1502

    Article  Google Scholar 

  • Shinozaki K, Yoda K, Hozumi K, Kira T (1964a) A quantitative analysis of plant form the pipe model theory. I. Basic analyses. Jap J Ecol 14:97–105

    Google Scholar 

  • Shinozaki K, Yoda K, Hozumi K, Kira T (1964b) A quantitative analysis of plant form the pipe model theory II. Further evidence of the theory and its application in forest ecology. Jap J Ecol 14:133–139

    Google Scholar 

  • Silvertown JW, Doust JL (1993) Introduction to plant population biology. Blackwell, London

    Google Scholar 

  • Sobrado MA (1997) Embolism vulnerability in drought-deciduous and evergreen species of a tropical dry forest. Acta Oecol 18:383–391. doi:10.1016/S1146-609X(97)80030-6

    Article  Google Scholar 

  • Sun S, Jin D, Shi P (2006) The leaf size–twig size spectrum of temperate woody species along an altitudinal gradient: an invariant allometric scaling relationship. Ann Bot (Lond) 97:97–107. doi:10.1093/aob/mcj004

    Article  Google Scholar 

  • Warton DI, Weber NC (2002) Common slope tests for bivariate structural relationships. Biometrical J 44:161–174. doi:10.1002/1521-4036(200203)44:2<161::AID-BIMJ161>3.0.CO;2-N

    Article  Google Scholar 

  • Warton DI, Wright IJ, Falster DS, Westoby M (2006) Bivariate line-fitting methods for allometry. Biol Rev Camb Philos Soc 81:259–291. doi:10.1017/S1464793106007007

    Article  PubMed  Google Scholar 

  • Westoby M, Falster DS, Moles AT, Vesk PA, Wright IJ (2002) Plant ecology strategies: some leading dimensions of variation between species. Annu Rev Ecol Syst 33:125–159. doi:10.1146/annurev.ecolsys.33.010802.150452

    Article  Google Scholar 

  • Westoby M, Wright IJ (2003) The leaf size-twig size spectrum and its relationship to other important spectra of variation among species. Oecologia 135:621–628

    PubMed  Google Scholar 

  • White PS (1983) Evidence that temperate east North American evergreen woody plants follow Corner’s rules. New Phytol 95:139–145. doi:10.1111/j.1469-8137.1983.tb03477.x

    Article  Google Scholar 

  • Wright IJ, Reich PB, Westoby M, Ackerly DD, Baruch Z, Bongers F, Cavender-Bares J, Chapin FS, Cornelissen JHC, Diemer M, Flexas J, Garnier E, Groom PK, Gulias J, Hikosaka K, Lamont BB, Lee T, Lee W, Lusk C, Midgley JJ, Navas ML, Niinemets Ü, Oleksyn J, Osada N, Poorter H, Poot P, Prior L, Pyankov VI, Roumet C, Thomas SC, Tjoelker MG, Veneklaas E, Villar R (2004) The world-wide leaf economics spectrum. Nature 428:821–827. doi:10.1038/nature02403

    Article  PubMed  CAS  Google Scholar 

  • Wright IJ, Falster DS, Pickup M, Westoby M (2006) Cross-species patterns in the coordination between leaf and stem traits, and their implications for plant hydraulics. Physiol Plant 127:445–456. doi:10.1111/j.1399-3054.2006.00699.x

    Article  CAS  Google Scholar 

  • Wright IJ, Ackerly DD, Bongers F, Harms KE, Ibarra-Manriquez G, Martinez-Ramos M, Mazer SJ, Muller-Landau HC, Paz H, Pitman NCA, Poorter L, Silman MR, Vriesendorp CF, Webb CO, Westoby M, Wright SJ (2007) Relationships among ecologically important dimensions of plant trait variation in seven Neotropical forests. Ann Bot (Lond) 99:1003–1015. doi:10.1093/aob/mcl066

    Article  Google Scholar 

  • Yang D, Li D, Sun S (2008) The generality of leaf size versus number tradeoff in temperate woody species. Ann Bot 102:623–629. doi:10.1093/aob/mcn135

    Article  PubMed  Google Scholar 

  • Zhong Y (1984) The vertical distribution of climate in the east slope of Mt. Emei in China. J Southwest China Norm Coll 5:111–116. Natural Science

    Google Scholar 

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Acknowledgments

We thank Xianming Gao, Guoyong Li, Dongmei Yang, Yanan Li, Yin Zou, Shuo Wang and Qin Shi for assistance in the field investigation, and Osbert Sun for English improvement. Thanks are also due to the staff of biological station at Mt. Emei for permitting this study to be conducted. The research was funded by the Chinese Academy of Sciences (KZCX2-XB2-02), National Science Foundation of China (30670333), and NCET to Shucun Sun.

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Correspondence to Shucun Sun.

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Communicated by S. Linder.

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Xiang, S., Wu, N. & Sun, S. Within-twig biomass allocation in subtropical evergreen broad-leaved species along an altitudinal gradient: allometric scaling analysis. Trees 23, 637–647 (2009). https://doi.org/10.1007/s00468-008-0308-6

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