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δ13C and water-use efficiency indicated by δ13C of different plant functional groups on Changbai Mountains, Northeast China

  • Articles/Geochemistry
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Chinese Science Bulletin

Abstract

Leaf δ 13C of different plant functional groups (trees, shrubs and forbs; evergreen and deciduous; annual, biennial and perennial) were examined on the Changbai Mountains, China. Life form has a significant influence on plant δ 13C, suggesting that leaf δ 13C is also ideal for distinguishing functional groups species in temperate and frigid zones with high humidity. Additionally, the difference of water-use efficiency (WUE) is significant among different plant functional groups. δ 13C and WUE are in the following order of forbs < shrubs < trees. Within shrubs, δ 13C and WUE are higher for evergreen shrubs than deciduous shrubs. Differences in δ 13C and WUE are significant among different lifespan herbs, and δ 13C and WUE follow the order of annual herbs > biennial herbs > perennial herbs, not in accordance with the pattern obtained by previous studies in deserts, suggesting that the ranking of δ 13C and WUE among annual, biennial and perennial herbs may be dependent on local water availability.

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References

  1. Shugart H H. Plant and ecosystem types. In: Smith T M, Shugart H H, Woodward F I, eds. Plant Functional Types: Their Relevance to Ecosystem Properties and Global Change. Cambridge: Cambridge University Press, 1997, 20–43

    Google Scholar 

  2. Domingues T F, Martinelli L A, Ehleringer J R. Ecophysiological traits of plant functional groups in forest and pasture ecosystems from eastern Amazônia, Brazil. Plant Ecol, 2007, 193: 101–112

    Article  Google Scholar 

  3. Farquhar G D, O’Leary M H, Berry J A. On the relationship between carbon isotope discrimination and the intercellular carbon dioxide concentration in leaves. Aust J Plant Physiol, 1982, 9: 121–137

    Article  Google Scholar 

  4. Farquhar G D, Richards P A. Isotopic composition of plant carbon correlates with water-use efficiency of wheat genotypes. Aust J Plant Physiol, 1984, 11: 539–552

    Google Scholar 

  5. Brooks J R, Flanagan L B, Buchmann N, et al. Carbon isotope composition of boreal plants: functional grouping of life forms. Oecologia, 1997, 110: 301–311

    Article  Google Scholar 

  6. Watkins J M Jr, Rundel P W, Cardelús C L. The influence of life forms on carbon and nitrogen relationships in tropical rainforest ferns. Oecologia, 2007, 153: 225–232

    Article  Google Scholar 

  7. Zheng S X, Shangguan Z P. Foliar δ 13C values of nine dominant species in the loess Plateau of China. Photosynthetica, 2007, 45: 110–119

    Article  Google Scholar 

  8. Ehleringer J R, Cooper T A. Correlations between carbon isotope ratio and microhabitat in desert plants. Oecologia, 1988, 76: 62–66

    Google Scholar 

  9. Lauteri M, Brugnoli E, Spaccino L. Carbon isotope discrimination in leaf soluble sugars and in whole plant dry matter in Helianthus annuus L. grown under different water conditions. In: Ehleringer J R, Hall A E, Farquhar G D, eds. Stable Isotope and Plant Carbon-Water Relations. San Diego: Academic Press, 1993. 93–108

    Google Scholar 

  10. Schuster W S F, Sandquist D R, Phillips S L, et al. Comparisons of carbon isotope discrimination in populations of aridland plant species differing in lifespan. Oecologia, 1992, 91: 332–337

    Article  Google Scholar 

  11. Su B, Han X G, Li L H, et al. Responses of δ 13C value and water use-efficiency of plant species to environmental gradients along the grassland zone of Northeast China Transect (in Chinese). Acta Phytoecol Sin, 2000, 24(6): 648–655

    Google Scholar 

  12. Peñuelas J, Filella I, Terradas J. Variability of plant nitrogen and water use in a 100-m transect of a subdesertic depression of the Ebro valley (Spain) characterized by leaf δ 13C and δ 15N. Acta Oecol, 1999, 20: 119–123

    Article  Google Scholar 

  13. Garten C T, Taylor G E. Foliar δ 13C within a temperate deciduous forest: spatial, temporal, and species sources of variation. Oecologia, 1992, 90: 1–7

    Article  Google Scholar 

  14. Kloeppel B D, Gower S T, Treichel I W, et al. Foliar carbon isotope discrimination in Larix species and sympatric evergreen conifers: a global comparison. Oecologia, 1998, 114: 153–159

    Article  Google Scholar 

  15. Marshall J D, Zhang J. Carbon isotope discrimination and water-use efficiency in native plants of the north-central Rockies. Ecology, 1994, 75: 1887–1895

    Article  Google Scholar 

  16. Smedley M P, Dawson T E, Comstock J P, et al. Seasonal carbon isotope discrimination in a grassland community. Oecologia, 1991, 85: 314–320

    Article  Google Scholar 

  17. Hinckley T M, Brooks J R, Cermak J, et al. Water flux in a hybrid poplar stand. Tree Physiol, 1994, 14: 1005–1018

    Google Scholar 

  18. Hollinger D Y, Kellher F M, Schulze E D, et al. Coupling of tree transpiration to atmospheric turbulence. Nature, 1994, 37: 160–162

    Google Scholar 

  19. Parker G G. Structure and microclimate of forest canopies. In: Lowman M D, Nadkarni N M, eds. Forest Canopies. San Diego: Academic Press, 1995. 73–106

    Google Scholar 

  20. Panek J A, Waring R H. Carbon isotope variation in Douglasfir foliage: improving the δ 13C-climate relationship. Tree Physiol, 1995, 15: 57–663

    Article  Google Scholar 

  21. Walcroft A S, Silvester W B, Grace J C, et al. Effects of branch length on carbon isotope discrimination in Pinus radiate. Tree Physiol, 1996, 16: 281–286

    Google Scholar 

  22. Brooks J R, Flanagan L B, Varney G T, et al. Vertical gradients of photosynthetic gas exchange and refixation of respired CO2 within boreal forest canopies. Tree Physiol, 1997, 117: 1–12

    Google Scholar 

  23. Schulze E D. Plant life forms and their carbon, water, and nutrient relations. In: Plant Physiological Ecology II. Berlin Heidelberg New York: Springer, 1982. 615–676

    Google Scholar 

  24. Chabot B F, Hicks D J. The ecology of leaf life spans. Annu Rev Ecol Syst, 1982, 13: 229–259

    Article  Google Scholar 

  25. Körner C H. Leaf diffusive conductance in the major vegetation types of the globe. In: Schulze E D, Caldwell M M, eds. Ecophysiology of Photosynthesis (Ecological Studies 100). Berlin Heidelberg New York: Springer, 1994. 463–490

    Google Scholar 

  26. Reich P B, Kloeppel B D, Ellsworth D S, et al. Different photosynthesis- nitrogen relations in deciduous hardwood and evergreen coniferous tree species. Oecologia, 1995, 104: 4–30

    Article  Google Scholar 

Download references

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Correspondence to GuoAn Wang.

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Supported by National Natural Science Foundation of China (Grant No. 40472159)

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Tan, W., Wang, G., Han, J. et al. δ13C and water-use efficiency indicated by δ13C of different plant functional groups on Changbai Mountains, Northeast China. Chin. Sci. Bull. 54, 1759–1764 (2009). https://doi.org/10.1007/s11434-009-0046-1

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  • DOI: https://doi.org/10.1007/s11434-009-0046-1

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