Carbon Isotope and Stomatal Data of Late Pliocene Betulaceae Leaves from SW China: Implications for Palaeoatmospheric CO2-levels

The cuticular d13C values and stomatal parameters (stomatal density and stomatal index: SD and SI) of two Betulaceae species, Betula mioluminifera Hu et Chaney and Carpinus miofangiana Nathorst, from a suite of superposed horizons in West Yunnan, southwestern China, were measured in order to recover Late Pliocene CO2 levels. Correlations are given for d13C, SD, epidermal cell density (ECD), and SI. d13C reveals a positive trend with the SD and SI in the two species, and such a positive correlation can also be observed between the d13C and ECD in C. miofangiana. However, d13C has a slightly negative correlation with the ECD in B. mioluminifera (R2= 0.06), possibly influenced by their different genotypes. Reflecting the changes through time, the d13C values of B. mioluminifera and C. miofangiana significantly increase with high determination coefficients (R2= 0.67 and R2= 0.65, respectively), as do SD (R2= 0.66 and R2= 0.51, respectively) and SI (R2= 0.50 and R2= 0.79, respectively). Research on extant B. luminifera and C. fangiana shows that the SD and especially SI, exhibit a prominent negative correlation with CO2 concentration. Pliocene CO2 levels are reconstructed as 381.5-439.4 ppmv and 377.8-472.3 ppmv, respectively, based on comparisons of the two fossil species with their nearest living equivalent (NLE) species. The significant positive trends of the d13C, SD and SI with ascending position of the fossils in the section indicate that the atmospheric CO2 levels declined in the Late Pliocene (3.30-2.83 Ma). Furthermore, the calculated CO2 levels are higher than in other studies and probably demonstrate that local CO2 enrichment can be caused by frequent volcanic eruptions over a long time scale

Carbon Isotope and Stomatal Data of Late Pliocene Betulaceae Leaves from SW China: Implications for Palaeoatmospheric CO2-levels

The cuticular d13C values and stomatal parameters (stomatal density and stomatal index: SD and SI) of two Betulaceae species, Betula mioluminifera Hu et Chaney and Carpinus miofangiana Nathorst, from a suite of superposed horizons in West Yunnan, southwestern China, were measured in order to recover Late Pliocene CO2 levels. Correlations are given for d13C, SD, epidermal cell density (ECD), and SI. d13C reveals a positive trend with the SD and SI in the two species, and such a positive correlation can also be observed between the d13C and ECD in C. miofangiana. However, d13C has a slightly negative correlation with the ECD in B. mioluminifera (R2= 0.06), possibly influenced by their different genotypes. Reflecting the changes through time, the d13C values of B. mioluminifera and C. miofangiana significantly increase with high determination coefficients (R2= 0.67 and R2= 0.65, respectively), as do SD (R2= 0.66 and R2= 0.51, respectively) and SI (R2= 0.50 and R2= 0.79, respectively). Research on extant B. luminifera and C. fangiana shows that the SD and especially SI, exhibit a prominent negative correlation with CO2 concentration. Pliocene CO2 levels are reconstructed as 381.5-439.4 ppmv and 377.8-472.3 ppmv, respectively, based on comparisons of the two fossil species with their nearest living equivalent (NLE) species. The significant positive trends of the d13C, SD and SI with ascending position of the fossils in the section indicate that the atmospheric CO2 levels declined in the Late Pliocene (3.30-2.83 Ma). Furthermore, the calculated CO2 levels are higher than in other studies and probably demonstrate that local CO2 enrichment can be caused by frequent volcanic eruptions over a long time scale

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  • Anderson, J.E., Williams, J., Kriedemann, P.E., Austin, M.P. & Farquhar, G.D. 1996. Correlations between carbon isotope discrimination and climate of native habitats for diverse eucalypt taxa growing in a common garden. Australian Journal of Plant Physiology 23, 311–320.
  • Aucour, A.M., Gomez B., Sheppard, S.M.F. & Thévenard, F. 2008. δC and stomatal number variability in the Cretaceous conifer Frenelopsis. Palaeogeography, Palaeoclimatology, Palaeoecology 257, 462–473.
  • Beerling, D.J., Mcelwain, J.C. & Osborne, C.P. 1998. Stomatal responses of the ‘living fossil’ Ginkgo biloba L. to changes in atmospheric CO2 concentrations. Journal of Experimental Botany 49, 1603–1607.
  • Beerling, D.J. & Royer, D.L. 2002. Fossil plants as indicators of the Phanerozoic global carbon cycle. Annual Review of Earth and Planetary Sciences 30, 527–556.
  • Beerling, D.J. & Woodward, F.I. 1995. Stomatal responses of variegated leaves to CO2 enrichment. Annals of Botany 75, 507–511.
  • Beerling, D.J. & Woodward, F.I. 1997. Changes in land plant function over the Phanerozoic: reconstructions based on the fossil record. Botanical Journal of the Linnean Society 124, 137–153.
  • Berner, R.A. 2006. GEOCARBSULF: A combined model for Phanerozoic atmospheric O2 and CO. Geochimica et Cosmochimica Acta 70, 5653–5664.
  • Berner, R.A. & Kothavala, Z. 2001. Geocarb III: A revised model of atmospheric CO2 over Phanerozoic time. American Journal of Science 301, 182–204.
  • Cerling, T.E., Wang, Y. & Quade, J. 1993. Expansion of C4 ecosystems as an indicator of global ecological change in the late Miocene. Nature 361, 344–345.
  • Chen, P.N., Wang, G.A., Han, J.M., Liu, X.J. & Liu, M. 2009. δ13C diff erence between plants and soil organic matter along the eastern slope of Mount Gongga. Chinese Science Bulletin 55, 55–62.
  • Craig, H. 1953. Th e geochemistry of the stable carbon isotopes. Geochimica et Cosmochimica Acta 3, 53–92.
  • Dai, J., Sun, B., Xie, S., Wu, J. & Li, N. 2009. Carpinus miofangiana from the Pliocene of Tengchong in Yunnan Province and its palaeoclimatic signifi cance. Advances in Earth Science 24, 1024–1032 [in Chinese, with English Abstract].
  • Ehleringer, J.R. & Cerling, T.E. 1995. Atmospheric CO2 and the ratio of intercellular to ambient CO2 concentration in plants. Tree Physiology 15, 105–111.
  • Ehleringer, J.R., Field, C.B. & Lin, Z.F. 1986. Leaf carbon isotope and mineral composition in subtropical plants along an irradiance cline. Oecologia 70, 520–526.
  • Farquhar, G.D., Ball, M.C., Von Caemmerer, S. & Roksandic, Z. 1982a. Eff ect of salinity and humidity on δ13C value of halophytes. Evidence for diff usional isotope fractionation determined by the ratio of intercellular/atmospheric partial pressure of CO2 under diff erent environmental conditions. Oecologia 52, 121–124.
  • Farquhar, G.D., O’leary, M.H. & Berry, J.A. 1982b. On the relationship between carbon isotope discrimination and the intercellular carbon dioxide concentration in leaves. Australian Journal of Plant Physiology 9, 121–137.
  • Farquhar, G.D., Ehleringer, J.R. & Hubick, K.T. 1989. Carbon isotope discrimination during photosynthesis. Annual Review of Plant Physiology and Plant Molecular Biology 40, 503–37.
  • Feng, X. 1999. Trends in intrinsic water–use effi ciency of natural trees for the past 100–200 years: a response to atmospheric CO2 concentration. Geochimica et Cosmochimica Acta 63, 1891–1903.
  • Francey, R.J., Allison, C.E., Etheridge, D.M., Trudinger, C.M., Enting, I.G., Leuenberger, M., Langenfelds, R.L., Michel, E. & Steele, L.P. 1999. A 1000–year high precision record of δ13C in atmospheric CO2. Tellus B 51, 170–193.
  • Franks, P.J. & Farquhar, G.D. 2007. Gas exchange, stomatal behavior, and δ13C values of the fl acca Tomato Mutant in relation to Abscisic Acid. Plant Physiology 143, 78–87.
  • Gay, A.P. & Hurd, R.G. 1975. Th e infuence of light on stomatal density in the tomato. New Phytologist 75, 37–46.
  • Ge, H.R. & Li, D.Y. 1999. Cenozoic Coal-bearing basins and coal forming regularity in west Yunnan. Yunnan Science and Technology Press, Kunming, China, 20–85 [in Chinese].
  • Gebrekirstos, A., Worbes, M., Teketay, D., Fetene, M. & Itlöhner, R. 2009. Stable carbon isotope ratios in tree rings of co-occurring species from semi-arid tropics in Africa: Patterns and climatic signals. Global and Planetary Change 66, 253–260.
  • Guo, G.Y. & Lin, Z.H. 1999. Discussion on late Cenozoic volcanic activities in Tengchong area, Yunnan Province, China. Contributions to Geology and Mineral Resources Research 14, 8–15 [in Chinese, with English abstract].
  • Harrison, T.M., Copeland, P., Kidd, W.S.F. & Lovera, O.M. 1995. Activation of the Nyainqentanglha Shear Zone, applications for uplift of the southern Tibet Plateau. Tectonics 14, 658–676.
  • Harrison, T.M., Copeland, P., Kidd, W.S.F. & Yin, A. 1992. Raising Tibet. Science 255, 1663–1670.
  • Ipcc (Intergovernmental Panel on Climate Change) 2007. Climate Change 2007: Th e Physical Science Basis. Summary for Policymakers. Contribution of Working Group I to the Fourth Assessment Report of the Intergovernmental Panel on Climate Change. IPCC WGI Fourth Assessment Report, 1–26.
  • Jahren, A.H., Lepage, B.A. & Werts, S.P. 2004. Methanogenesis in Eocene Arctic soils inferred from δ13C of tree fossil carbonates. Palaeogeography, Palaeoclimatology, Palaeoecology 214, 347– 358.
  • Jiang, C.S. 1998. Period division of volcano activities in the Cenozoic era of Tengchong. Journal of Seismological Research 21, 320– 329 [in Chinese, with English abstract].
  • Keeling, C.D., Mook, W.M. & Tans, P. 1979. Recent trends in the 13C/12C ratio of atmospheric carbon dioxide. Nature 277, 121– 123.
  • Kouwenberg, L.L.R., Kürschner, W.M. & Mcelwain, J.C. 2007. Stomatal frequency change over altitudinal gradients: prospects for paleoaltimetry. Reviews in Mineralogy and Geochemistry 66, 215–241.
  • Kürschner, W.M. 2002. Carbon isotope composition of fossil leaves – revealing ecophysiological responses to past environmental change. New Phytologist 155, 199–201.
  • Kürschner, W.M., Van Der Burgh, J., Visscher, H. & Dilcher, D.L. 1996. Oak leaves as biosensors of late Neogene and early Pleistocene paleoatmospheric CO2 concentrations. Marine Micropaleontology 27, 299–312.
  • Li, D.M., Li, Q. & Chen, W.J. 2000. Volcanic activities in the Tengchong volcano area since Pliocene. Acta Petrologica Sinica 16, 362–370 [in Chinese, with English Abstract].
  • Li, F., & Xue, C.D. 1999. Geodynamic setting since the Cenozoic and its environmental eff ects in Northwest Yunnan, China. Geotectonica et Metallogenia 23, 115–122 [in Chinese, with English abstract].
  • Lockheart, M.J., Poole, I., Van Bergen, P.F. & Evershed, R.P. 1998. Leaf carbon isotope compositions and stomatal characters: important considerations for palaeoclimate reconstructions. Organic Geochemistry 29, 1003–1008.
  • McElwain, J.C. 1998. Do fossil plants signal palaeoatmospheric CO2 concentration in the geological past? Philosophical Transactions of the Royal Society B 353, 83–96.
  • McElwain, J.C. 2004. Climate-independent paleoaltimetry using stomatal density in fossil leaves as a proxy for CO partial pressure. Geology 32, 1017–1020.
  • McElwain, J.C. & Chaloner, W.G. 1995. Stomatal density and index of fossil plants track atmospheric carbon dioxide in the Paleozoic. Annals of Botany 76, 389–395.
  • McElwain, J.C. & Chaloner, W.G. 1996. Th e fossil cuticle as a skeletal record of environmental change. Palaios 11, 376–388.
  • Minami, M., Goto, A.S., Omori, T., Ohta, T. & Nakamura, T. 2010. Comparison of δ13C and 14C activities of CO2 samples combusted in closed-tube and elemental-analyzer systems. Nuclear Instruments and Methods in Physics Research Section B 268, 914–918.
  • Molnar, P. & England, P. 1990. Late Cenozoic uplift of mountain ranges and global climate change: chicken or egg? Nature 346, 29–34.
  • Pagani, M., Liu, Z., Lariviere, J. & Ravelo, A.C. 2010. High Earth- system climate sensitivity determined from Pliocene carbon dioxide concentrations. Nature Geoscience 3, 27–30.
  • Peters-Kottig, W., Strauss, H. & Kerp H. 2006. Th e land plant δ13C record and plant evolution in the Late Palaeozoic. Palaeogeography, Palaeoclimatology, Palaeoecology 240, 237– 252.
  • Polley, H.W., Johnson, H.B., Marino B.D. & Mayeux, H.S. 1993. Increase in C3 plant water-use effi ciency and biomass over Glacial to present CO2 concentrations. Nature 361, 61–63.
  • Poole, I. & Kürschner, W. M. 1999. Stomatal density and index: the practice. In: Jones, T.P. & Rowe, N.P. (eds), Fossil Plant and Spores: Modern Techniques. Th e Geological Society, London, UK, 257–260.
  • Quade, J.,  Cerling, T.E. & Bowman, J.R. 1989. Development of Asian monsoon revealed by marked ecological shift during the latest Miocene in northern Pakistan. Nature 342, 163–166.
  • Rajabi, A., Ober, E.S. & Griffiths, H. 2009. Genotypic variation for water use effi ciency, carbon isotope discrimination, and potential surrogate measures in sugar beet. Field Crops Research 112, 172–181.
  • Retallack, G.J. 2001. A 300-million-year record of atmospheric carbon dioxide from fossil plant cuticles. Nature 411, 287–290.
  • Royer, D.L. 2001. Stomatal density and stomatal index as indicators of paleoatmospheric CO2 oncentration. Review of Palaeobotany and Palynology 114, 1–28.
  • Royer, D.L., Berner, R.A. & Beerling, D.J. 2001. Phanerozoic atmospheric CO2 change: evaluating geochemical and paleobiological approaches. Earth–Science Reviews 54, 349– 392.
  • Salisbury, E.J. 1927. On the causes and ecological signifi cance of stomatal frequency, with special reference to the Woodland fl ora. Philosophical Transactions of the Royal Society of London B 216, 1–65.
  • Shang, Y.L. 2003. Tengchong diatomite deposit and its genesis. Yunnan Geology 22, 418–425 [in Chinese, with English abstract].
  • Sharma, G.K. & Dunn, D.B. 1968. Eff ect of environment on the cuticular features in Kalanchoe fedschenkoi. Bulletin of the Torrey Botanical Club 95, 464–473.
  • Sun, B.N., Cong, P.Y., Yan, D.F. & Xie, S.P. 2003. Cuticular structure of two angiosperm fossils in Neogene from Tengchong, Yunnan Province and its palaeoenvironmental signifi cance. Acta Palaeontologica Sinica 42, 216–222 [in Chinese, with English abstract].
  • Sun, B.N., Xiao, L., Xie, S.P., Deng, S.H., Wang, Y.D., Jia, H. & Turner, S. 2007. Quantitative analysis of paleoatmospheric CO2 level based on stomatal characters of fossil Ginkgo from Jurassic to Cretaceous in China. Acta Geologica Sinca 81, 931– 939.
  • Sun, B.N., Wu, J.Y., Liu, Y.S., Ding, S.T., Li, X.C., Xie, S.P., Yan, D.F. & Lin, Z.C. 2011. Reconstructing Neogene vegetation and climates to infer tectonic uplift in western Yunnan, China. Palaeogeography, Palaeoclimatology, Palaeoecology 304, 328−336.
  • Sun, H.L. & Zheng, D. 2003. Formation, Environment and Development of Qinghai–Xizang (Tibetan) Plateau. Shijiazhuang: Hebei Science & Technology Press, Shijiazhuang, China [in Chinese].
  • Tang, J. & Qian, J. 2000. Restructing CO2 concentration by the tree- ring carbon isotopic ratios of West Tianmu Mountain. Journal of Nanjing Forestry University 24, 45–48 [in Chinese, with English abstract].
  • Tans, P.P. & White, J.W.C. 1998. In balance, with a little help from the plants. Science 281, 183–184.
  • Tao, J.R. & Du, N.Q. 1982. Neogene fl ora of Tengchong basin in western Yunnan, China. Journal of Integrative Plant Biology 24, 273–281 [in Chinese, with English Abstract].
  • Tripati, A.K., Roberts, C.D. & Eagle, R.A. 2009. Coupling of CO2 and ice sheet stability over major climate transitions of the last 20 million years. Science 326, 1394–1397.
  • Tu, T.T.N., Kürschner, W.A., Schouten, S. & Van Bergen, P.F. 2004. Leaf carbon isotope composition of fossil and extant oaks grown under diff ering atmospheric CO2 levels. Palaeogeography, Palaeoclimatology, Palaeoecology 212, 199– 213.
  • Van Der Burgh, J., Vissher, H., Dilcher, D.L. & Kürschner, W.M. 1993. Paleoatmospheric signatures in Neogene fossil leaves. Science 260, 1788–1790.
  • Van De Water, P.K., Leavitt, S.W. & Betancourt, J.L. 2002. Leaf δ13C variability with elevation, slope aspect, and precipitation in the southwest United States. Oecologia 132, 332–343.
  • Wignall, P.B. 2001. Large igneous provinces and mass extinctions. Earth-Science Reviews 53, 1–33.
  • Woodward, F.I. 1987. Stomatal numbers are sensitive to increases in CO2 from pre-industrial levels. Nature 327, 617–18.
  • Wu, J.Y. 2009. Th e Pliocene Tuantian Flora of Tengchong, Yunnan Province and its Paleoenvironmental Analysis. PhD. Th esis, Lanzhou University, Lanzhou, China.
  • Wu, J.Y., Sun, B.N., Liu, Y.S., Xie, S.P. & Lin, Z.C. 2009. A new species of Exbucklandia (Hamamelidaceae) from the Pliocene of China and its paleoclimatic signiŞcance. Review of Palaeobotany and Palynology 155, 32–41.
  • Xu, J.X., Ferguson, D.K., Li, C.S., Wang, Y.F. & Du, N.Q. 2004. Climatic and ecological implications of Late Pliocene Palynofl ora from Longling, Yunnan, China. Quaternary International 117, 91–103.
  • Xu, J.X., Ferguson, D.K., Li, C.S. & Wang, Y.F. 2008. Late Miocene vegetation and climate of the Lühe region in Yunnan, southwestern China. Review of Palaeobotany and Palynology 148, 36–59.
  • Zhu, L., Liang, Z.S., Xu, X., Li, S.H. & Monneveux, P. 2009. Evidences for the association between carbon isotope discrimination and grain yield — Ash content and stem carbohydrate in spring wheat grown in Ningxia (Northwest China). Plant Science 176, 758–767.
  • Zimmerman, J.K. & Ehleringer, J.R. 1990. Carbon isotope ratios are correlated with irradiance levels in the Panamanian orchid catasetum viridifl avam. Oecologia 83, 247–249.
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