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Leaf flushing and shedding, bud and flower production, and stem elongation in tall birch trees subjected to increases in aboveground temperature

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Tall birch trees allocate extra resource due to aboveground temperature elevation to bud and male flower production rather than to plant growth. Saplings increased only plant growth under warming. Size-dependent response should be considered.

Abstract

We experimentally heated canopy organs of tall birch trees (Betula ermanii Cham.; 18–20 m high) growing at a high latitude to determine how leaf phenology, plant growth, and bud and male flower production might shift in response to increases in aboveground temperature during global climate change. We warmed the canopies with infrared heat lamps fixed to steel pipe scaffolds built around the trees. The temperature of the warmed canopies increased by approximately 1 °C. Warming extended the length of the growing season of canopy leaves (by accelerating leaf flush and delaying leaf fall), and significantly increased the numbers of buds and male flowers per shoot. Bud production and shoot length were positively correlated in both warmed and control branches. However, warming did not increase canopy shoot lengths. The intercept value of the positive regression slope between bud production and shoot length for warmed branches was higher than that for control branches. Thus, canopy warming had a direct positive effect on the bud production but had no indirect effect via increases in shoot length. Our experiment showed that tall birch trees allocated extra resources made available by increased aboveground temperature to bud and male flower production rather than to plant growth.

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References

  • Arft AM, Walker MD, Gurevitch J et al (1999) Response of tundra plants to experimental tundra experiment. Ecol Monogr 69:491–511. doi:10.1890/0012-9615(1999)069[0491:ROTPTE]2.0.CO;2

  • Aronson EL, McNulty SG (2009) Appropriate experimental ecosystem warming methods by ecosystem, objective, and practicality. Agric For Meteorol 149:1791–1799. doi:10.1016/j.agrformet.2009.06.007

    Article  Google Scholar 

  • Augspurger CK, Bartlett EA (2003) Differences in leaf phenology between juvenile and adult trees in a temperate deciduous forest. Tree Physiol 23:517–525. doi:10.1093/treephys/23.8.517

    Article  PubMed  Google Scholar 

  • Basset Y, Horlyck V, Wright J (2003) Forest canopies and their importance. In: Basset Y, Horlyck V, Wright J (eds) Studying forest canopies from above: the international canopy crane network. Smithsonian Tropical Research Institute and UNEP, Panama, pp 27–34

    Google Scholar 

  • Bond BJ, Czarnomski NM, Cooper C et al (2000) Developmental decline in height growth in Douglas-fir. Tree Physiol 27:441–453. doi:10.1093/treephys/27.3.441

    Article  Google Scholar 

  • Chung H, Muraoka H, Nakamura M et al (2013) Experimental warming studies on tree species and forest ecosystems: a literature review. J Plant Res 126:447–460. doi:10.1007/s10265-013-0565-3

    Article  PubMed  Google Scholar 

  • de Kroon H, Huber H, Stuefer JF et al (2005) A modular concept of phenotypic plasticity in plants. New Phytol 166:73–82. doi:10.1111/j.1469-8137.2004.01310.x

    Article  PubMed  Google Scholar 

  • Delagrange S, Messier C, Lechowicz MJ et al (2004) Physiological, morphological and allocational plasticity in understory deciduous trees: importance of plant size and light availability. Tree Physiol 24:775–784. doi:10.1093/treephys/24.7.775

    Article  PubMed  Google Scholar 

  • Hiura T, Fujiwara K, Hojo G et al (1995) Stand structure and long-term dynamics of primeval forests in Nakagawa Experimental Forest, Hokkaido University. Res Bull Hokkaido Univ For 52:85–94 (in Japanese with English summary)

    Google Scholar 

  • Hyvönen R, Ågren GI, Linder S et al (2007) The likely impact of elevated [CO2], nitrogen deposition, increased temperature and management on carbon sequestration in temperate and boreal forest ecosystems: a literature review. New Phytol 173:463–480. doi:10.1111/j.1469-8137.2007.01967.x

    Article  PubMed  Google Scholar 

  • IPCC (2014) Climate change 2014: synthesis report. In: Core Writing Team, Pachauri RK, Meyer LA (eds) Contribution of Working Groups 1, 2 and 3 to the fifth assessment report of the intergovernmental panel on climate change. IPCC, Geneva, p 151

    Google Scholar 

  • Ishii HT, Tanabe S, Hiura T (2004) Exploring the relationships among canopy structure, stand productivity, and biodiversity of temperate forest ecosystems. For Sci 50:342–355

    Google Scholar 

  • Knight TM, Steets JA, Vamosi JC et al (2005) Pollen limitation of plant reproduction: pattern and process. Ann Rev Ecol Evol Syst 36:467–497. doi:10.1146/annurev.ecolsys.36.102403.115320

    Article  Google Scholar 

  • Masaka K, Maguchi S (2001) Modelling the masting behaviour of Betula platyphylla var. japonica using the resource budget model. Ann Bot 88:1049–1055. doi:10.1006/anbo.2001.1547

    Article  Google Scholar 

  • Nabeshima E, Kubo T, Hiura T (2010) Variation in tree diameter growth in response to the weather conditions and tree size in deciduous broad-leaved trees. For Ecol Manag 259:1055–1066. doi:10.1016/j.foreco.2009.12.012

    Article  Google Scholar 

  • Nakamura M, Muller O, Tayanagi S et al (2010) Experimental branch warming alters tall tree leaf phenology and acorn production. Agric For Meteorol 150:1026–1029. doi:10.1016/j.agrformet.2010.04.001

    Article  Google Scholar 

  • Nakamura M, Nakaji T, Muller O et al (2014) Different initial responses of the canopy herbivory rate in mature oak trees to experimental soil and branch warming in a soil-freezing area. Oikos 124:1071–1077. doi:10.1111/oik.01940

    Article  Google Scholar 

  • Niu SL, Li ZX, Xia JY et al (2008) Climatic warming changes plant photosynthesis and its temperature dependence in a temperate steppe of northern China. Environ Exp Bot 63:91–101. doi:10.1016/j.envexpbot.2007.10.1016

    Article  Google Scholar 

  • Rustad LE, Campbell JL, Marion GM et al (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. doi:10.1007/s004420000544

    Article  Google Scholar 

  • Saxe H, Cannell MGR, Johnsen Ø et al (2001) Tree and forest functioning in response to global warming. New Phytol 149:369–400. doi:10.1046/j.1469-8137.2001.00057.x

    Article  CAS  Google Scholar 

  • Shaver GR, Canadell J, Chapin FS (2000) Global warming and terrestrial ecosystems: a conceptual framework for analysis. Bioscience 50:871–882. doi:10.1641/0006-3568(2000)050[0871:GWATEA]2.0.CO;2

  • Shen KP, Harte J (2000) Ecosystem climate manipulation. In: Sala OER, Jackson B, Mooney HA et al (eds) Methods in ecosystem science. Springer, New York, pp 353–369

    Chapter  Google Scholar 

  • Sugiyama S, Bazzas FA (1998) Size dependence of reproductive allocation: the influence of resource availability, competition and genetic identity. Funct Ecol 12:280–288. doi:10.1046/j.1365-2435.1998.00187.x

    Article  Google Scholar 

  • Tatewaki M, Igarashi T (1971) Forest vegetation in the Teshio and the Nakagawa district experimental forest of Hokkaido University, Prov. Teshio, N. Hokkaido, Japan. Res Bull Coll Exp For Hokkaido Univ 28:1–192 (in Japanese with English summary)

    Google Scholar 

  • Turnbull MH, Tissue DT, Merthy R et al (2004) Noctunal warming increases photosynthesis at elevated CO2 partial pressure in Populus detoides. New Phytol 161:819–826. doi:10.1111/j.1469-8137.2004.00994.x

    Article  Google Scholar 

  • Vitasse Y (2013) Ontogenetic changes rather than difference in temperature cause understory trees to leaf out earlier. New Phytol 198:149–155. doi:10.1111/nph.12130

    Article  PubMed  Google Scholar 

  • Weiner J, Thomas SC (2001) The nature of tree growth and the age-related decline in forest productivity. Oikos 94:374–376. doi:10.1034/j.1600-0706.2001.940219.x

    Article  Google Scholar 

  • Xu Z, Hu T, Zhang Y (2012) Effects of experimental warming on phenology, growth and gas exchange of treeline birch (Betula utilis) sapling, Eastern Tibetan Plateau, China. Eur J For Res 131:811–819. doi:10.1007/s10342-011-0554-9

    Article  Google Scholar 

  • Yasaka M, Kobayashi S, Takeuchi S et al (2009) Prediction of birch airborne pollen counts by examining male catkin numbers in Hokkaido, northern Japan. Aerobiologia 25:111–117. doi:10.1007/s10453-009-9116-8

    Article  Google Scholar 

Download references

Acknowledgments

We thank staff members at Nakagawa Experimental Forest Hokkaido University for their support during the study. This work was supported by Grants from the Japan Society for the Promotion of Science (No. 26450188 to MN and Nos. 19657007 and 21248017 to TH) and the Ministry of Environment (S-9-3 to TH).

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Correspondence to Masahiro Nakamura.

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Communicated by G. Piovesan.

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Nakamura, M., Makoto, K., Tanaka, M. et al. Leaf flushing and shedding, bud and flower production, and stem elongation in tall birch trees subjected to increases in aboveground temperature. Trees 30, 1535–1541 (2016). https://doi.org/10.1007/s00468-016-1387-4

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  • DOI: https://doi.org/10.1007/s00468-016-1387-4

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