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Photosynthesis, carboxylation and leaf nitrogen responses of 16 species to elevated pCO 2 across four free-air CO 2 enrichment experiments in forest, grassland and desert

dc.contributor.authorEllsworth, David S.en_US
dc.contributor.authorReich, Peter B.en_US
dc.contributor.authorNaumburg, Elke S.en_US
dc.contributor.authorKoch, George W.en_US
dc.contributor.authorKubiske, Mark E.en_US
dc.contributor.authorSmith, Stan D.en_US
dc.date.accessioned2010-06-01T19:41:54Z
dc.date.available2010-06-01T19:41:54Z
dc.date.issued2004-12en_US
dc.identifier.citationEllsworth, David S.; Reich, Peter B.; Naumburg, Elke S.; Koch, George W.; Kubiske, Mark E.; Smith, Stan D. (2004). "Photosynthesis, carboxylation and leaf nitrogen responses of 16 species to elevated pCO 2 across four free-air CO 2 enrichment experiments in forest, grassland and desert." Global Change Biology 10(12): 2121-2138. <http://hdl.handle.net/2027.42/72832>en_US
dc.identifier.issn1354-1013en_US
dc.identifier.issn1365-2486en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/72832
dc.description.abstractThe magnitude of changes in carboxylation capacity in dominant plant species under long-term elevated CO 2 exposure (elevated pC a ) directly impacts ecosystem CO 2 assimilation from the atmosphere. We analyzed field CO 2 response curves of 16 C 3 species of different plant growth forms in favorable growth conditions in four free-air CO 2 enrichment (FACE) experiments in a pine and deciduous forest, a grassland and a desert. Among species and across herb, tree and shrub growth forms there were significant enhancements in CO 2 assimilation ( A ) by +40±5% in elevated pC a (49.5–57.1 Pa), although there were also significant reductions in photosynthetic capacity in elevated pC a in some species. Photosynthesis at a common pC a ( A a ) was significantly reduced in five species growing under elevated pC a , while leaf carboxylation capacity ( V cmax ) was significantly reduced by elevated pC a in seven species (change of −19±3% among these species) across different growth forms and FACE sites. Adjustments in V cmax with elevated pC a were associated with changes in leaf N among species, and occurred in species with the highest leaf N. Elevated pC a treatment did not affect the mass-based relationships between A or V cmax and N, which differed among herbs, trees and shrubs. Thus, effects of elevated pC a on leaf C assimilation and carboxylation capacity occurred largely through changes in leaf N, rather than through elevated pC a effects on the relationships themselves. Maintenance of leaf carboxylation capacity among species in elevated pC a at these sites depends on maintenance of canopy N stocks, with leaf N depletion associated with photosynthetic capacity adjustments. Since CO 2 responses can only be measured experimentally on a small number of species, understanding elevated CO 2 effects on canopy N m and N a will greatly contribute to an ability to model responses of leaf photosynthesis to atmospheric CO 2 in different species and plant growth forms.en_US
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dc.format.extent3109 bytes
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dc.publisherBlackwell Science Ltden_US
dc.rights© 2004 Blackwell Publishing Ltden_US
dc.subject.otherDownregulationen_US
dc.subject.otherElevated CO 2en_US
dc.subject.otherFree-air CO 2 Enrichmenten_US
dc.subject.otherLeaf Carboxylation Capacityen_US
dc.subject.otherLeaf Nitrogenen_US
dc.subject.otherNitrogen Allocation to RuBP Carboxylase Enzymeen_US
dc.subject.otherPhotosynthesis–Nitrogen Relationshipsen_US
dc.subject.otherPhotosynthetic Nitrogen-use Efficiencyen_US
dc.subject.otherPlant Functional Groupsen_US
dc.titlePhotosynthesis, carboxylation and leaf nitrogen responses of 16 species to elevated pCO 2 across four free-air CO 2 enrichment experiments in forest, grassland and deserten_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbsecondlevelGeology and Earth Sciencesen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumSchool of Natural Resources and Environment, University of Michigan, 430 East University Ave., Ann Arbor, MI 48109, USA ,en_US
dc.contributor.affiliationother† Department of Forest Resources, University of Minnesota, St Paul, MN 55108, USA ,en_US
dc.contributor.affiliationother† Department of Biological Sciences, University of Nevada-Las Vegas, Las Vegas, NV 89154, USA ,en_US
dc.contributor.affiliationother§ Department of Biological Sciences, Northern Arizona University, Flagstaff, AZ 86011, USA ,en_US
dc.contributor.affiliationother¶ USDA Forest Service, North Central Research Station, Forestry Sciences Lab 5985 Hwy K, Rhinelander, WI 54501, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/72832/1/j.1365-2486.2004.00867.x.pdf
dc.identifier.doi10.1111/j.1365-2486.2004.00867.xen_US
dc.identifier.sourceGlobal Change Biologyen_US
dc.identifier.citedreferenceAber JD, Reich PB, Goulden ML ( 1996 ) Extrapolating leaf CO 2 exchange to the canopy: a generalized model of forest photosynthesis validated by eddy correlation. Oecologia, 106, 267 – 275.en_US
dc.identifier.citedreferenceAinsworth EA, Davey PA, Hymus GJ et al. ( 2003 ) Is stimulation of leaf photosynthesis by elevated carbon dioxide concentration maintained in the long term? A test with Lolium perenne grown for 10 years at two nitrogen fertilization levels under Free Air CO 2 Enrichment (FACE). Plant Cell and Environment, 26, 705 – 714.en_US
dc.identifier.citedreferenceBaldocchi D, Meyers T ( 1998 ) On using eco-physiological, micrometeorological and biogeochemical theory to evaluate carbon dioxide, water vapor and trace gas fluxes over vegetation: a perspective. Agricultural and Forest Meteorology, 90, 1 – 25.en_US
dc.identifier.citedreferenceBassiriRad H, Constable JVH, Lussenhop J et al. ( 2003 ) Widespread foliage delta N-15 depletion under elevated CO 2: inferences for the nitrogen cycle. Global Change Biology, 9, 1582 – 1590.en_US
dc.identifier.citedreferenceBassiriRad H, Gutschick VP, Lussenhop J ( 2001 ) Root system adjustments: regulation of plant nutrient uptake and growth responses to elevated CO 2. Oecologia, 126, 305 – 320.en_US
dc.identifier.citedreferenceBernacchi CJ, Singsaas EL, Pimentel C et al. ( 2001 ) Improved temperature response functions for models of Rubisco-limited photosynthesis. Plant Cell and Environment, 24, 253 – 260.en_US
dc.identifier.citedreferenceCanadell JG, Mooney HA, Baldocchi DD et al. ( 2000 ) Carbon metabolism of the terrestrial biosphere: a multitechnique approach for improved understanding. Ecosystems, 3, 115 – 130.en_US
dc.identifier.citedreferenceCrous KY, Ellsworth DS ( 2004 ) Canopy position affects photosynthetic adjustments to long-term CO 2 enrichment in a mature Pinus taeda L. forest. Tree Physiology, 24, 961 – 970.en_US
dc.identifier.citedreferenceCurtis PS ( 1996 ) A meta-analysis of leaf gas exchange and nitrogen in trees grown under elevated carbon dioxide. Plant Cell and Environment, 19, 127 – 137.en_US
dc.identifier.citedreferenceCurtis PS, Wang XZ ( 1998 ) A meta-analysis of elevated CO 2 effects on woody plant mass, form, and physiology. Oecologia, 113, 299 – 313.en_US
dc.identifier.citedreferenceDiaz S, Grime JP, Harris J et al. ( 1993 ) Evidence of a feedback mechanism limiting plant-response to elevated carbon dioxide. Nature, 364, 616 – 617.en_US
dc.identifier.citedreferenceDickson RE, Lewin KF, Isebrands JG et al. ( 2000 ) USDA Forest Service North Central Experiment Station, General Technical Report NC-214, pp. 1–68.en_US
dc.identifier.citedreferenceDrake BG, GonzÀlez-Meler MA, Long SP ( 1997 ) More efficient plants: a consequence of rising atmospheric CO 2 ? Annual Review of Plant Physiology and Plant Molecular Biology, 48, 609 – 639.en_US
dc.identifier.citedreferenceEllsworth DS ( 2000 ) Seasonal CO 2 assimilation and stomatal limitations in a Pinus taeda canopy. Tree Physiology, 20, 435 – 445.en_US
dc.identifier.citedreferenceEvans JR ( 1989 ) Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia, 78, 9 – 19.en_US
dc.identifier.citedreferenceEvans JR, Poorter H ( 2001 ) Photosynthetic acclimation of plants to growth irradiance: the relative importance of specific leaf area and nitrogen partitioning in maximizing carbon gain. Plant Cell and Environment, 24, 755 – 767.en_US
dc.identifier.citedreferenceEvans JR, Von Caemmerer S ( 1996 ) Carbon dioxide diffusion inside leaves. Plant Physiology, 110, 339 – 346.en_US
dc.identifier.citedreferenceFarquhar GD, Von Caemmerer S, Berry JA ( 1980 ) A biochemical model of photosynthetic CO 2 assimilation in leaves of C 3 species. Planta, 149, 78 – 90.en_US
dc.identifier.citedreferenceField CB, Chapin III FS, Matson PA et al. ( 1992 ) Responses of terrestrial ecosystems to the changing atmosphere: a resource-based approach. Annual Review of Ecology and Systematics, 23, 201 – 235.en_US
dc.identifier.citedreferenceField CB, Mooney HA ( 1986 ) In: On the Economy of Plant form and Function ( ed. Givnish TJ ), pp. 25 – 55. Cambridge University Press, Cambridge, MA.en_US
dc.identifier.citedreferenceGriffin KL, Tissue DT, Turnbull MH et al. ( 2000 ) The onset of photosynthetic acclimation to elevated CO 2 partial pressure in field-grown Pinus radiata D. Don. after 4 years. Plant Cell and Environment, 23, 1089 – 1098.en_US
dc.identifier.citedreferenceGunderson CA, Wullschleger SD ( 1994 ) Photosynthetic acclimation in trees to rising atmospheric CO 2 – a broader perspective. Photosynthesis Research, 39, 369 – 388.en_US
dc.identifier.citedreferenceHendrey GR, Ellsworth DS, Lewin KF et al. ( 1999 ) A free-air enrichment system for exposing tall forest vegetation to elevated atmospheric CO 2. Global Change Biology, 5, 293 – 309.en_US
dc.identifier.citedreferenceHikosaka K, Hirose T ( 1998 ) Leaf and canopy photosynthesis of C3 plants at elevated CO 2 in relation to optimal partitioning of nitrogen among photosynthetic components: theoretical prediction. Ecological Modelling, 106, 247 – 259.en_US
dc.identifier.citedreferenceHu S, Chapin FS, Firestone MK et al. ( 2001 ) Nitrogen limitation of microbial decomposition in a grassland under elevated CO 2. Nature, 409, 188 – 191.en_US
dc.identifier.citedreferenceHuxman TE, Hamerlynck EP, Moore BD et al. ( 1998 ) Photosynthetic down-regulation in Larrea tridentata exposed to elevated atmospheric CO 2: interactions with drought under glasshouse and field conditions. Plant Cell and Environment, 21, 1153 – 1161.en_US
dc.identifier.citedreferenceJordan DN, Zitzer SF, Hendrey GR et al. ( 1999 ) Biotic, abiotic and performance aspects of the Nevada desert free-air CO 2 enrichment (FACE) facility. Global Change Biology, 5, 659 – 669.en_US
dc.identifier.citedreferenceKÖrner C ( 2000 ) Biosphere responses to CO 2 enrichment. Ecological Applications, 10, 1590 – 1619.en_US
dc.identifier.citedreferenceKÖrner C, Pelaez-Riedl S, van Bel AJE ( 1995 ) CO 2 responsiveness of plants – a possible link to phloem-loading. Plant Cell and Environment, 18, 595 – 600.en_US
dc.identifier.citedreferenceLee TD, Reich PB, Tjoelker MG ( 2003 ) Legume presence increases photosynthesis and N concentrations of co-occurring non-fixers but does not modulate their responsiveness to carbon dioxide enrichment. Oecologia, 137, 22 – 31.en_US
dc.identifier.citedreferenceLee TD, Tjoelker MG, Ellsworth DS et al. ( 2001 ) Leaf gas exchange responses of 13 prairie grassland species to elevated CO 2 and increased nitrogen supply. New Phytologist, 150, 405 – 418.en_US
dc.identifier.citedreferenceLewin KF, Hendrey GR, Nagy J et al. ( 1994 ) Design and application of a free-air carbon dioxide enrichment facility. Agricultural and Forest Meteorology, 70, 15 – 29.en_US
dc.identifier.citedreferenceLuo Y, Field CB, Mooney HA ( 1994 ) Predicting responses of photosynthesis and root fraction to elevated CO 2 (a) – interactions among carbon, nitrogen, and growth. Plant Cell and Environment, 17, 1195 – 1204.en_US
dc.identifier.citedreferenceMcMurtrie RE, Medlyn BE, Dewar RC ( 2001 ) Increased understanding of nutrient immobilization in soil organic matter is critical for predicting the carbon sink strength of forest ecosystems over the next 100 years. Tree Physiology, 21, 831 – 839.en_US
dc.identifier.citedreferenceMedlyn BE, Badeck FW, De Pury DGG et al. ( 1999 ) Effects of elevated CO 2 on photosynthesis in European forest species: a meta-analysis of model parameters. Plant Cell and Environment, 22, 1475 – 1495.en_US
dc.identifier.citedreferenceMoore BD, Cheng SH, Sims D et al. ( 1999 ) The biochemical and molecular basis for photosynthetic acclimation to elevated atmospheric CO 2. Plant Cell and Environment, 22, 567 – 582.en_US
dc.identifier.citedreferenceNaumburg E, Housman DC, Huxman TE et al. ( 2003 ) Photosynthetic responses of Mojave Desert shrubs to free air CO 2 enrichment are greatest during wet years. Global Change Biology, 9, 276 – 285.en_US
dc.identifier.citedreferenceNoormets A, McDonald EP, Dickson RE et al. ( 2001a ) The effect of elevated carbon dioxide and ozone on leaf- and branch-level photosynthesis and potential plant-level carbon gain in aspen. Trees-Structure and Function, 15, 262 – 270.en_US
dc.identifier.citedreferenceNoormets A, Sober A, Pell EJ et al. ( 2001b ) Stomatal and non-stomatal limitation to photosynthesis in two trembling aspen ( Populus tremuloides Michx.) clones exposed to elevated CO 2 and/or O 3. Plant Cell and Environment, 24, 327 – 336.en_US
dc.identifier.citedreferencePearcy RW, BjÖrkman O ( 1983 ) Physiological effects. In: CO 2 and Plants: The Response of Plants to Rising Levels of Atmospheric Carbon Dioxide. AAAS Selected Symposium, Vol. 84 ( ed. Lemon E ), pp. 65 – 105. American Association for Advancement of Science, Washington, DC.en_US
dc.identifier.citedreferencePeterson AG, Field CB, Ball JT et al. ( 1999 ) Reconciling the apparent difference between mass- and area-based expressions of photosynthesis–nitrogen relationship. Oecologia, 118, 144 – 150.en_US
dc.identifier.citedreferencePoorter H ( 1993 ) Interspecific variation in the growth response of plants to an elevated CO 2 concentration. Vegetatio, 104/105, 77 – 97.en_US
dc.identifier.citedreferencePoorter H ( 1998 ) Do slow-growing species and nutrient-stressed plants respond relatively strongly to elevated CO 2 ? Global Change Biology, 4, 693 – 697.en_US
dc.identifier.citedreferencePoorter H, Evans JR ( 1998 ) Photosynthetic nitrogen-use efficiency of species that differ inherently in specific leaf area. Oecologia, 116, 26 – 37.en_US
dc.identifier.citedreferenceReich PB, Ellsworth DS, Walters MB ( 1998 ) Leaf structure (specific leaf area) modulates photosynthesis–nitrogen relations: evidence from within and across species and functional groups. Functional Ecology, 12, 948 – 958.en_US
dc.identifier.citedreferenceReich PB, Ellsworth DS, Walters MB et al. ( 1999 ) Generality of leaf trait relationships: a test across six biomes. Ecology, 80, 1955 – 1969.en_US
dc.identifier.citedreferenceReich PB, Kloeppel BD, Ellsworth DS et al. ( 1995 ) Different photosynthesis–nitrogen relations in deciduous hardwood and evergreen coniferous tree species. Oecologia, 104, 24 – 30.en_US
dc.identifier.citedreferenceReich PB, Knops J, Tilman D et al. ( 2001 ) Plant diversity enhances ecosystem responses to elevated CO 2 and nitrogen deposition. Nature, 410, 809 – 812.en_US
dc.identifier.citedreferenceRoderick M, Berry SL, Noble I ( 1999 ) The relationship between leaf composition and morphology at elevated CO 2 concentrations. New Phytologist, 143, 63 – 72.en_US
dc.identifier.citedreferenceRogers A, Ellsworth DS ( 2002 ) Photosynthetic acclimation of Pinus taeda (loblolly pine) to long-term growth in elevated pCO (2) (FACE). Plant Cell and Environment, 25, 851 – 858.en_US
dc.identifier.citedreferenceSage RF ( 1994 ) Acclimation of photosynthesis to increasing atmospheric CO 2 – the gas exchange perspective. Photosynthesis Research, 39, 351 – 368.en_US
dc.identifier.citedreferenceSage RF, Sharkey TD, Seemann JR ( 1989 ) Acclimation of photosynthesis to elevated CO 2 in five C 3 species. Plant Physiology, 89, 590 – 596.en_US
dc.identifier.citedreferenceSaxe H, Ellsworth DS, Heath J ( 1998 ) Tree and forest functioning in an enriched CO 2 atmosphere. New Phytologist, 139, 395 – 436.en_US
dc.identifier.citedreferenceSellers PJ, Bounoua L, Collatz GJ et al. ( 1996 ) Comparison of radiative and physiological effects of doubled atmospheric CO 2 on climate. Science, 271, 1402 – 1406.en_US
dc.identifier.citedreferenceSmith SD, Huxman TE, Zitzer S et al. ( 2000 ) Elevated CO 2 increases productivity and invasive species success in an arid ecosystem. Nature, 408, 79 – 82.en_US
dc.identifier.citedreferenceSokal RR, Rohlf FJ ( 1995 ) Biometry. W.H. Freeman, New York, NY.en_US
dc.identifier.citedreferenceStitt M ( 1991 ) Rising CO 2 levels and their potential significance for carbon flow in photosynthetic cells. Plant Cell and Environment, 14, 741 – 762.en_US
dc.identifier.citedreferenceStitt M, Krapp A ( 1999 ) The interaction between elevated carbon dioxide and nitrogen nutrition: the physiological and molecular background. Plant Cell and Environment, 22, 583 – 621.en_US
dc.identifier.citedreferenceWohlfahrt G, Bahn M, Haubner E et al. ( 1999 ) Interspecific variation of the biochemical limitation to photosynthesis and related leaf traits of 30 species from mountain grassland ecosystems under different land use. Plant Cell and Environment, 22, 1281 – 1296.en_US
dc.identifier.citedreferenceWullschleger SD ( 1993 ) Biochemical limitations to carbon assimilation in C 3 plants – a retrospective analysis of the A/Ci curves from 109 Species. Journal of Experimental Botany, 44, 907 – 920.en_US
dc.identifier.citedreferenceYin X ( 2002 ) Responses of leaf nitrogen concentration and specific leaf area to atmospheric CO 2 enrichment: a retrospective analysis. Global Change Biology, 8, 631 – 642.en_US
dc.identifier.citedreferenceZak DR, Holmes WE, Finzi AC et al. ( 2003 ) Soil nitrogen cycling under elevated CO 2: a synthesis of forest FACE experiments. Ecological Applications, 13, 1508 – 1514.en_US
dc.identifier.citedreferenceZak DR, Pregitzer KS, Curtis PS et al. ( 2000 ) Atmospheric CO 2, soil-N availability, and allocation of biomass and nitrogen by Populus tremuloides. Ecological Applications, 10, 34 – 46.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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