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Seasonal variation of temperature response of respiration in invasive Berberis thunbergii (Japanese barberry) and two co-occurring native understory shrubs in a northeastern US deciduous forest

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Abstract

In the understory of a closed forest, plant growth is limited by light availability, and early leafing is proposed to be an important mechanism of plant invasion by providing a spring C “subsidy” when high light is available. However, studies on respiration, another important process determining plant net C gain, are rare in understory invasive plants. In this study, leaf properties and the temperature response of leaf respiration were compared between invasive Berberis thunbergii, an early leafing understory shrub, and two native shrubs, Kalmia latifolia, a broadleaf evergreen and Vaccinium corymbosum, a late-leafing deciduous species, in an oak-dominated deciduous forest. The seasonal trend of the basal respiration rates (R 0) and the temperature response coefficient (E 0), were different among the three shrubs and species-specific negative correlations were observed between R 0 and E 0. All three shrubs showed significant correlation between respiration rate on an area basis (20°C) and leaf N on an area basis. The relationship was attributed to the variation of both leaf N on a mass basis and leaf mass per area (LMA) in B. thunbergii, but to LMA only in K. latifolia and V. corymbosum. After modeling leaf respiration throughout 2004, B. thunbergii displayed much higher annual leaf respiration (mass based) than the two native shrubs, indicating a higher cost per unit of biomass investment. Thus, respiratory properties alone were not likely to lead to C balance advantage of B. thunbergii. Future studies on whole plant C budgets and leaf construction cost are needed to address the C balance advantage in early leafing understory shrubs like B. thunbergii.

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References

  • Agren GI, Axelsson B (1980) Population respiration: a theoretical approach. Ecol Model 11:39–54

    Article  Google Scholar 

  • Amthor JS (1989) Respiration and crop productivity. Springer, New York

    Google Scholar 

  • Atkin OK, Tjoelker MG (2003) Thermal acclimation and the dynamic response of plant respiration to temperature. Trends Plant Sci 8:343–351

    Article  PubMed  CAS  Google Scholar 

  • Atkin OK, Holly C, Ball MC (2000) Acclimation of snow gum (Eucalyptus pauciflora) leaf respiration to seasonal and diurnal variations in temperature: the importance of changes in the capacity and temperature sensitivity of respiration. Plant Cell Environ 23:15–26

    Article  Google Scholar 

  • Baars R, Kelly D (1996) Survival and growth responses of native and introduced vines in New Zealand to light availability. N Z J Bot 34:389–400

    Google Scholar 

  • Barringer K, Clemants SE (2003) The vascular flora of Black Rock Forest, Cornwall, New York. J Torrey Bot Soc 130:292–308

    Article  Google Scholar 

  • Bolstad PV, Mitchell K, Vose JM (1999) Foliar temperature-respiration response functions for broad-leaved tree species in the southern Appalachians. Tree Physiol 19:871–878

    PubMed  Google Scholar 

  • Dewar RC, Medlyn BE, McMurtrie RE (1999) Acclimation of the respiration photosynthesis ratio to temperature: insights from a model. Global Change Biol 5:615–622

    Article  Google Scholar 

  • Dungan RJ, Whitehead D, Duncan RP (2003) Seasonal and temperature dependence of photosynthesis and respiration for two co-occurring broad-leaved tree species with contrasting leaf phenology. Tree Physiol 23:561–568

    PubMed  CAS  Google Scholar 

  • Engel VC, Stieglitz M, Williams M, Griffin KL (2002) Forest canopy hydraulic properties and catchment water balance: observations and modeling. Ecol Model 154:263–288

    Article  Google Scholar 

  • Finzi AC, Canham CD (2000) Sapling growth in response to light and nitrogen availability in a southern New England forest. For Ecol Manage 131:153–165

    Article  Google Scholar 

  • Givnish TJ (2002) Adaptive significance of evergreen versus deciduous leaves: solving the triple paradox. Silva Fenn 36:703–743

    Google Scholar 

  • Griffin KL, Turnbull M, Murthy R (2002) Canopy position affects the temperature response of leaf respiration in Populus deltoides. New Phytol 154:609–619

    Article  Google Scholar 

  • Gunnarsson U (2005) Global patterns of Sphagnum productivity. J Bryol 27:269–279

    Article  Google Scholar 

  • Harrington RA, Brown BJ, Reich PB (1989) ecophysiology of exotic and native shrubs in southern Wisconsin.1. Relationship of leaf characteristics, resource availability, and phenology to seasonal patterns of carbon gain. Oecologia 80:356–367

    Article  Google Scholar 

  • IPCC (2007) Fouth assessment report of Working Group I. United Nations Environment Programme, Geneva

    Google Scholar 

  • Lloyd J, Taylor JA (1994) On the temperature-dependence of soil respiration. Funct Ecol 8:315–323

    Article  Google Scholar 

  • Loveys BR, Atkinson LJ, Sherlock DJ, Roberts RL, Fitter AH, Atkin OK (2003) Thermal acclimation of leaf and root respiration: an investigation comparing inherently fast and slow-growing plant species. Global Change Biol 9:895–910

    Article  Google Scholar 

  • Lyons JM, Raison JK (1970) Oxidative activity of mitochondria isolated from plant tissues sensitive and resistant to chilling injury. Plant Physiol 45:386

    Article  PubMed  CAS  Google Scholar 

  • Myers CV, Anderson RC (2003) Seasonal variation in photosynthetic rates influences success of an invasive plant, garlic mustard (Alliaria petiolata). Am Midl Nat 150:231–245

    Article  Google Scholar 

  • Reich PB, et al. (1998a) Relationships of leaf dark respiration to leaf nitrogen, specific leaf area and leaf life-span: a test across biomes and functional groups. Oecologia 114:471–482

    Article  Google Scholar 

  • Reich PB, Walters MB, Tjoelker MG, Vanderklein D, Buschena C (1998b) Photosynthesis and respiration rates depend on leaf and root morphology and nitrogen concentration in nine boreal tree species differing in relative growth rate. Funct Ecol 12:395–405

    Article  Google Scholar 

  • Rosenzweig C, Solecki WD (2001) Climate change and a global city: the potential consequences of climate variability and change: metro east coast, report for the US. Global change research program, national assessment of the potential consequences of climate variability and change for the United States. Columbia Earth Institute, New York

    Google Scholar 

  • Ryan MG (1991) Effects of climate change on plant respiration. Ecol Appl 1:157–167

    Article  Google Scholar 

  • Ryan MG (1995) Foliar maintenance respiration of sub-alpine and boreal trees and shrubs in relation to nitrogen-content. Plant Cell Environ 18:765–772

    Article  CAS  Google Scholar 

  • Ryan MG, Hubbard RM, Pongracic S, Raison RJ, McMurtrie RE (1996) Foliage, fine-root, woody-tissue and stand respiration in Pinus radiata in relation to nitrogen status. Tree Physiol 16:333–343

    PubMed  Google Scholar 

  • Sliander JA, Klepeis DM (1999) The invasion ecology of Japanese barberry (Berberis thunbergii) in the New England landscape. Biol Inv 1:189–201

    Article  Google Scholar 

  • Taylor JR (1982) An introduction to error analysis: the study of uncertainties if physical measurements. Oxford University Press, Oxford

    Google Scholar 

  • Tissue DT, Lewis JD, Wullschleger SD, Amthor JS, Griffin KL, Anderson OR (2002) Leaf respiration at different canopy positions in sweetgum (Liquidambar styraciflua) grown in ambient and elevated concentrations of carbon dioxide in the field. Tree Physiol 22:1157–1166

    PubMed  Google Scholar 

  • Turnbull MH, Whitehead D, Tissue DT, Schuster WSF, Brown KJ, Griffin KL (2001) Responses of leaf respiration to temperature and leaf characteristics in three deciduous tree species vary with site water availability. Tree Physiol 21:571–578

    PubMed  CAS  Google Scholar 

  • Turnbull MH, Whitehead D, Tissue DT, Schuster WSF, Brown KJ, Griffin KL (2003) Scaling foliar respiration in two contrasting forest canopies. Funct Ecol 17:101–114

    Article  Google Scholar 

  • Turnbull MH, Tissue DT, Griffin KL, Richardson SJ, Peltzer DA, Whitehead D (2005) Respiration characteristics in temperate rainforest tree species differ along a long-term soil-development chronosequence. Oecologia 143:271–279

    Article  PubMed  Google Scholar 

  • Vose JM, Ryan MG (2002) Seasonal respiration of foliage, fine roots, and woody tissues in relation to growth, tissue N, and photosynthesis. Global Change Biol 8:182–193

    Article  Google Scholar 

  • Walters MB, Reich PB (1999) Low-light carbon balance and shade tolerance in the seedlings of woody plants: do winter deciduous and broad-leaved evergreen species differ? New Phytol 143:143–154

    Article  Google Scholar 

  • Whitehead D, et al. (2004) Response of total night-time respiration to differences in total daily photosynthesis for leaves in a Quercus rubra L. canopy: implications for modelling canopy CO2 exchange. Global Change Biol 10:925–938

    Article  Google Scholar 

  • Xu CY (2006) Foliar dark respiration: scaling gas exchange characteristics and isotopic signals from leaf to canopy and ecosystem level. PhD thesis, Columbia University

  • Xu CY, Griffin KL (2006) Seasonal variation in the temperature response of leaf respiration in Quercus rubra: foliage respiration and leaf properties. Funct Ecol 20:778–789

    Article  Google Scholar 

  • Zotz G, Franke M, Woitke M (2000) Leaf phenology and seasonal carbon gain in the invasive plant, Bunias orientalis L. Plant Biol 2:653–658

    Article  Google Scholar 

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Acknowledgements

We thank the Black Rock Forest staff for their assistance throughout the experiment and for access to the field site. This research was supported by the Black Rock Forest Consortium through the Stiefel Foundation Small Grants for Scientific Research. We also thank the reviewers and subject editor for their helpful critical comments.

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Correspondence to Cheng-Yuan Xu.

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Communicated by Robert Pearcy.

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Xu, CY., Schuster, W.S.F. & Griffin, K.L. Seasonal variation of temperature response of respiration in invasive Berberis thunbergii (Japanese barberry) and two co-occurring native understory shrubs in a northeastern US deciduous forest. Oecologia 153, 809–819 (2007). https://doi.org/10.1007/s00442-007-0790-3

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  • DOI: https://doi.org/10.1007/s00442-007-0790-3

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