Aalto, T. and Juurola, E. (2002). A three-dimensional model of CO2 transport in airspaces and mesophyll cells of a silver birch leaf. Plant, Cell and Environment, 25, 1399–1409.CrossRefGoogle Scholar

Aasamaa, K., Sober, A. and Rahi, M. (2001). Leaf anatomical characteristics associated with hydraulic conductance, stomatal conductance and stomatal sensitivity to changes of leaf water status in temperate deciduous trees. Australian Journal of Plant Physiology, 28, 765–774.Google Scholar

Aasamaa, K., Sõber, A., Hartung, W., et al. (2002). Rate of stomatal opening, shoot hydraulic conductance and photosynthesis characteristics in relation to leaf abscisic acid concentration in six temperate deciduous trees. Tree Physiology, 22, 267–276.CrossRefGoogle ScholarPubMed

Aasamaa, K., Sõber, A., Hartung, W., et al. (2004). Drought acclimation of two deciduous tree species of different layers in a temperate forest canopy. Trees: Structure and Function, 18, 93–101.Google Scholar

Abadía, J., Morales, F. and Abadía, A. (1999). Photosystem II efficiency in low chlorophyll, iron-deficient leaves. Plant and Soil, 215, 183–192.CrossRefGoogle Scholar

Abadía, J., Nishio, J.N. and Terry, N. (1986). Chlorophyll-protein and polypeptide composition of Mn-deficient sugar beet thylakoids. Photosynthesis Research, 7, 379–381.CrossRefGoogle ScholarPubMed

Abbink, T.E.M., Peart, J.R., Mos, T.N.M., et al. (2002). Silencing of a gene encoding a protein component of the oxygen-evolving complex of Photosystem II enhances virus replication in plants. Virology, 295, 307–319.CrossRefGoogle ScholarPubMed

Abe, H., Urao, T., Ito, T., et al. (2003). Arabidopsis AtMYC2 (bHLH) and AtMYB2 (MYB) function as transcriptional activators in abscisic acid signaling. Plant Cell, 15, 63–78.CrossRefGoogle ScholarPubMed

Abeledo, J.G., Calderini, D.F. and Slafer, G.A. (2003). Genetic improvement of barley yield potential and its physiological determinants in Argentina (1944–1998). Euphytica, 130, 325–334.CrossRefGoogle Scholar

Abeles, F.B. (1986). Plant Chemiluminescence. Annual Review of Plant Physiology, 37, 49–72.CrossRefGoogle Scholar

Aber, J.D., Reich, P.B. and Goulden, M.L. (1996). Extrapolating leaf CO2 exchange to the canopy: a generalized model of forest photosynthesis compared with measurements by eddy correlation. Oecologia, 106, 257–265.CrossRefGoogle ScholarPubMed

Abrams, M.D. (1996). Distribution, historical development and ecophysiological attributes of oak species in the eastern United States. Annales des Sciences Forestieres, 53, 487–512.CrossRefGoogle Scholar

Ache, P., Bauer, H., Kollist, H., et al. (2010). Stomatal action directly feeds back on leaf turgor: new insights into the regulation of the plant water status from non-invasive pressure probe measurements. The Plant Journal, 62, 1072–1082.Google ScholarPubMed

Ackerly, D. (1997). Allocation, leaf display, and growth in fluctuating light environments. In: Plant Resource Allocation (eds Bazzaz, F. A. and Grace, J.). Academic Press, San Diego.

Adams, K.L. and Wendel, J.F. (2005). Polyploidy and genome evolution in plants. Current Opinion in Plant Biology, 8, 135–141.CrossRefGoogle ScholarPubMed

Adams, M.L., Norvell, W.A., Peverly, J.H., et al. (1993). Fluorescence and reflectance characteristics of manganese deficient soybean leaves: effects of leaf age and choice of leaflet. Plant and Soil, 155/156, 235–238.CrossRefGoogle Scholar

Adams, M.S. and Strain, B.R. (1968). Photosynthesis in stems and leaves of Cercidium floridum: spring and summer diurnal field response and relation to temperature. Oecologia Plantarum, 3, 285–297.Google Scholar

Adams, P., Nelson, D.E., Yamada, S., et al. (1998). Growth and development of Mesembryanthemum crystallinum (Aizoaceae). New Phytologist, 138, 171–190.CrossRefGoogle Scholar

Adams, W.W. III and Demmig-Adams, B. (1994). Carotenoid composition and down regulation of photosystem II in three conifer species during the winter. Physiologia Plantarum, 92, 451–458.CrossRefGoogle Scholar

Adams, W.W. III, Demmig-Adams, B., Rosenstiel, T.N., et al. (2002). Photosynthesis and photoprotection in overwintering plants. Plant Biology, 4, 535–654.Google Scholar

Adams, W.W. III, Demmig-Adams, B., Verhoeven, A.S., et al. (1995). ‘Photoinhibition’ during winter stress: involvement of sustained xanthophyll cycle-dependent energy dissipation. Australian Journal of Plant Physiology, 22, 261–276.CrossRefGoogle Scholar

Adams, W.W. III, Demmig-Adams, B., Winter, K., et al. (1990a). The ratio of variable to maximum chlorophyll fluorescence from photosystem II, measured at room temperature and 77K, as indicator of the photon yield of photosynthesis. Planta, 180, 166–174.CrossRefGoogle Scholar

Adams, W.W. III, Winter, K. and Lanzl, A. (1989). Light and the maintenance of photosynthetic competence in leaves of Populus balsamifera L. during short-term exposures to high concentrations of sulfur dioxide. Planta, 177, 91–97.CrossRefGoogle ScholarPubMed

Adams, W.W. III, Winter, K., Schreiber, U., et al. (1990b). Photosynthesis and chlorophyll fluorescence characteristics in relationship to changes in pigment and element composition of leaves of Platanus occidentalis L. during autumnal leaf senescence. Plant Physiology, 93, 1184–1190.CrossRefGoogle Scholar

Affek, H.P., Krisch, M.J. and Yakir, D. (2006). Effects of intraleaf variations in carbonic anhydrase activity and gas echange on leaf C18OO isoflux in Zea mays. New Phytologist, 169, 321–329.CrossRefGoogle Scholar

Aganchich, B., Wahbi, S., Loreto, F., et al. (2009). Partial root zone drying: regulation of photosynthetic limitations and antioxidant enzymatic activities in young olive (Olea europaea) saplings. Tree Physiology, 29, 685–696.CrossRefGoogle ScholarPubMed

Agati, G., Cerovic, Z.G. and Moya, I. (2000). The effect of decreasing temperature up to chilling values on the in vivo F685/F735 chlorophyll fluorescence ratio in Phaseolus vulgaris and Pisum sativum. The role of the photosystem I contribution to the 735 nm fluorescence band. Photochemistry and Photobiology, 72, 75–84.2.0.CO;2>CrossRefGoogle ScholarPubMed

Agati, G., Cerovic, Z.G., Dalla Marta, A., et al. (2008). Optically assessed preformed flavonoids and susceptibility of grapevine to Plasmopora viticola under different light regimes. Functional Plant Biology, 35, 77–84.CrossRefGoogle Scholar

Agati, G., Galardi, C., Gravano, E., et al. (2002). Flavonoid distribution in tissues of Phillyrea latifolia L. leaves as estimated by microspectrofluorometry and multispectral fluorescence microimaging. Photochemistry and Photobiology, 76, 350–360.2.0.CO;2>CrossRefGoogle ScholarPubMed

Agati, G., Mazzinghi, P., Fusi, F., et al. (1995). The F685/730 chlorophyll fluorescence ratio as a tool in plant physiology: response to physiological and environmental factors. Journal of Plant Physiology, 145, 228–238.CrossRefGoogle Scholar

Agati, G., Meyer, S., Matteini, P., et al. (2007). Assessment of anthocyanins in grape (Vitis vinifera L.) berries using a noninvasive chlorophyll fluorescence method. Journal of Agricultural and Food Chemistry, 55, 1053–1061.CrossRefGoogle ScholarPubMed

Agbariah, K.T. and Roth-Bejerano, N. (1990). The effect of blue light on energy levels in epidermal strips. Physiologia Plantarum, 78, 100–104.CrossRefGoogle Scholar

Ågren, G.I. and Ingestad, T. (1987). Root:shoot ratio as a balance between nitrogen productivity and photosynthesis. Plant Cell Environment, 10, 579–586.Google Scholar

Aguirreolea, J., Irigoyen, J., Sánchez-Díaz, M., et al. (1995). Physiological alterations in pepper during wilt induced by Phytophthora capsici and soil water deficit. Plant Pathology, 44, 587–596.CrossRefGoogle Scholar

Agustí, S., Enríquez, S., Frost-Christensen, H., et al. (1994). Light harvesting among photosynthetic organisms. Functional Ecology, 8, 273–279.CrossRefGoogle Scholar

Agustynowicz, J. and Gabrys, H. (1999). Chloroplast movements in fern leaves: correlation of movement dynamics and environmental flexibility of the species. Plant, Cell and Environment, 22, 1239–1248.CrossRefGoogle Scholar

Aharon, R., Shahak, Y., Wininger, S., et al. (2003). Overexpression of a plasma membrane aquaporin in transgenic tobacco improves plant vigor under favourable growth conditions but not under drought or salt stress. The Plant Cell, 15, 439–447.CrossRefGoogle ScholarPubMed

Ahn, T.K., Avenson, T.J., Ballottari, M., et al. (2008). Architecture of a charge-transfer state regulating light harvesting in a plant antenna protein. Science, 320, 794–797.CrossRefGoogle Scholar

Ainsworth, E., Davey, P., Bernacchi, C., et al. (2002). A meta-analysis of elevated [CO2] effects on soybean (Glycine max) physiology, growth and yield. Global Change Biology, 8, 695–709.CrossRefGoogle Scholar

Ainsworth, E., Leakey, A., Ort, D., et al. (2008b). FACE-ing the facts: inconsistencies and interdependence among field, chamber and modeling studies of elevated [CO2] impacts on crop yield and food supply. New Phytologist, 179, 5–9.CrossRefGoogle ScholarPubMed

Ainsworth, E.A. (2008). Rice production in a changing climate: a meta-analysis of responses to elevated carbon dioxide and elevated ozone concentration. Global Change Biology, 14, 1642–1650.CrossRefGoogle Scholar

Ainsworth, E.A. and Long, S.P. (2005). What have we learned from 15 years of free-air CO2 enrichment (FACE)? A meta-analytic review of the responses of photosynthesis, canopy properties and plant production to rising CO2. New Phytologist, 165, 351–372.CrossRefGoogle ScholarPubMed

Ainsworth, E.A. and Rogers, A. (2007). The response of photosynthesis and stomatal conductance to rising [CO2]: mechanisms and environmental interactions. Plant, Cell and Environment, 30, 258–270.CrossRefGoogle Scholar

Ainsworth, E.A., Davey, P.A., Hymus, G.J., 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 CO2 enrichment (FACE). Plant, Cell and Environment, 26, 705–714.CrossRefGoogle Scholar

Ainsworth, E.A., Rogers, A. and Leakey, A.D.B. (2008a). Targets for crop biotechnology in a future high CO2 and HighO3 world. Plant Physiology, 147, 13–19.CrossRefGoogle Scholar

Ainsworth, E.A., Rogers, A.Nelson, R., et al. (2004). Testing the “source-sink” hypothesis of down-regulation of photosynthesis in elevated CO2 in the field with single gene substitutions in Glycine max. Agricultural and Forest meteorology, 122, 85–94.CrossRefGoogle Scholar

Akhani, H., Barroca, J., Koteeva, N., et al. (2005). Bienertia sinuspersici (Chenopodiaceae): A new species from southwest Asia and discovery of a third terrestrial C4 plant without Kranz anatomy. Systematic Botany, 30, 290–301.CrossRefGoogle Scholar

Akhani, H., Trimborn, P. and Ziegler, H. (1997). Photosynthetic pathways in Chenopodiaceae from Africa, Asia and Europe with their ecological, phytogeographical and taxonomical importance. Plant Systematics and Evolution, 206, 187–221.CrossRefGoogle Scholar

Al-Abbas, A.H., Barr, R., Hall, J.D., et al. (1974). Spectra of normal and nutrient deficient maize leaves. Agronomy Journal, 66, 16–20.CrossRefGoogle Scholar

Alboresi, A., Gerotto, C., Giacometti, G.M., et al. (2010). Physcomitrella patens mutants affected on heat dissipation clarify the evolution of photoprotection mechanisms upon land colonization. Proceedings of the National Academy of Sciences USA, 107, 11128–11133.CrossRefGoogle ScholarPubMed

Aldea, M., Frank, T.D. and DeLucia, E.H. (2006a). A method for quantitative analysis of spatially variable physiological processes across leaf surfaces. Photosynthesis Research, 90, 161–172.CrossRefGoogle ScholarPubMed

Aldea, M., Hamilton, J.G., Resti, J.P., et al. (2005). Indirect effects of insect herbivory on leaf gas exchange in soybean. Plant, Cell and Environment, 28, 402–411.CrossRefGoogle Scholar

Aldea, M., Hamilton, J.G., Resti, J.P., et al. (2006b). Comparison of photosynthetic damage from arthropod herbivory and pathogen infection in understory hardwood saplings. Oecologia, 149, 221–232.CrossRefGoogle ScholarPubMed

Al-Hazmi, M., Lakso, A.N. and Denning, S.S. (1997). Whole canopy versus single leaf gas exchange responses to water stress in Cabernet Sauvignon grapevines. In: Proceedings of the IVth International Symposium on Cool Climate Viticulture and Enology (eds Edson, C., Wolf, T., Pool, R., Reynolds, A., Henick-Kling, T., Acree, T., Reisch, B. and Harkness, E.), Eastern Section, Am. Soc. Enol. Vitic., Geneva, NY, USA, pp. II.47-II.48.Google Scholar

Ali, B., Hasan, S.A., Hayat, S., et al. (2008). A role for brassinosteroids in the amelioration of aluminium stress through antioxidant system in mung bean (Vigna radiata L. Wilczek). Environmental and Experimental Botany, 62, 153–159.CrossRefGoogle Scholar

Allard, V., Ourcival, J.M., Rambal, S., et al. (2008). Seasonal and annual variation of carbon exchange in an evergreen Mediterranean forest in southern France. Global Change Biology, 14, 1–12.CrossRefGoogle Scholar

Allen, D.J. and Ort, D.R. (2001). Impacts of chilling temperatures on photosynthesis in warm-climate plants. Trends Plant Sciences, 6, 36–42.CrossRefGoogle ScholarPubMed

Allen, D.J., Ratner, K., Giller, Y.E., et al. (2000). An overnight chill induces a delayed inhibition of photosynthesis at midday in mango (Mangifera indica L.). Journal of Experimental Botany, 51, 1893–1902.CrossRefGoogle Scholar

Allen, D.K., Shachar-Hill, Y. and Ohlrogge, J.B. (2007). Compartment-specific labeling information in 13C metabolic flux analysis of plants. Phytochemistry, 68, 2197–2210.CrossRefGoogle Scholar

Allen, J.F. (1992). How does protein phosphorylation regulate photosynthesis?Trends in Biochemical Sciences, 17, 12–17.CrossRefGoogle ScholarPubMed

Allen, J.F. (2003). Cyclic, pseudocyclic and noncyclic photophosphorylation: new links in the chain. Trends Plant Sciences, 8, 15–19.CrossRefGoogle ScholarPubMed

Allen, J.F. and Forsberg, J. (2001). Molecular recognition in thylakoid structure and function. Trends Plant Sciences, 6, 317–326.CrossRefGoogle ScholarPubMed

Allen, J.F. and Nilsson, A. (1997). Redox signalling and the structural basis of regulation of photosynthesis by protein phosphorylation. Physiologia Plantarum, 100, 863–868.CrossRefGoogle Scholar

Allen, L.H., Pan, D., Boote, K.J., et al. (2003). Carbon dioxide and temperature effects on evapotranspiration and water use efficiency of soybean. Agronomy Journal, 95, 1071–1081.CrossRefGoogle Scholar

Allen, M.F. (1991). The Ecology of Mycorrhizae. Cambridge University Press, Cambridge, UK.Google Scholar

Almási, A., Harsányi, A. and Gáborjányi, R. (2001). Photosynthetic alterations on virus infected plants. Acta Phytopathologica et Entomologica Hungarica, 36, 15–29.CrossRefGoogle Scholar

Alo, C.A. and Wang, G.L. (2008). Potential future changes of the terrestrial ecosystem based on climate projections by eight general circulation models. Journal of Geophysical Research – Biogeosciences, 113, Article number G01004.CrossRefGoogle Scholar

Alongi, D.M., Ayukai, T., Brunskill, G.J., et al. (1998). Sources, sinks and export of organic carbon through a tropical, semi-enclosed delta (Hinchinbrook Channel, Australia). Mangrove and Salt Marshes, 2, 237–242.CrossRefGoogle Scholar

Alonso, A.A. and Machado, S.R. (2007). Morphological and developmental investigations of the underground system of Erythroxylum species from Brazilian cerrado. Australian Journal of Botany, 55, 749–758.CrossRefGoogle Scholar

Alterio, G., Giorio, P. and Sorrentino, G. (2006). Open-system chamber for measurements of gas exchanges at plant level. Environmental Science and Technology, 40, 1950–1955.CrossRefGoogle ScholarPubMed

Altesor, A., Ezcurra, E. and Silva, C. (1992). Changes in the photosynthetic metabolism during early ontogeny of four cactus species. Acta Oecologica, 13, 777–785.Google Scholar

Althawadi, A.M. and Grace, J. (1986). Water use by the desert cucurbit Citrullus colocynthis (L.) Schrad. Oecologia, 70, 475–480.CrossRefGoogle ScholarPubMed

Amthor, J.S. (1991). Respiration in a future, higher-CO2 world. Plant Cell and Environment, 14, 13–20.CrossRefGoogle Scholar

Amthor, J.S. (1994). Scaling CO2-photosynthesis relationships from the leaf to the canopy. Photosynthesis Research, 39, 321–350.CrossRefGoogle ScholarPubMed

Amthor, J.S. (2000). The McCree–de Wit–Penning de Vries–Thornley respiration paradigms: 30 years later. Annals of Botany, 86, 1–20.CrossRefGoogle Scholar

Amthor, J.S. (2007). Improving photosynthesis and yield potential. In: Improvement of Crop Plants for Industrial End Uses, (ed. Ramalli, P.), Springer, NY, USA, pp. 27–58.Google Scholar

Amthor, J.S., Goulden, M.L., Munger, J.W., et al. (1994). Testing a mechanistic model of forest-canopy mass and energy exchange using eddy correlation: carbon dioxide and ozone uptake by a mixed oak-maple stand. Australian Journal of Plant Physiology, 21, 623–651.CrossRefGoogle Scholar

Ananyev, G.S., Kolber, Z.S., Klimov, D., et al. (2005). Remote sensing of heterogeneity in photosynthetic efficiency, electron transport and dissipation of excess light in Populus deltoides stands under ambient and elevated CO2 concentrations, and in a tropical forest canopy, using a new laser-induced fluorescence transient device. Global Change Biology, 11, 1195–1206.CrossRefGoogle Scholar

Anderson, D.E. and Verma, S.B. (1986). Carbon dioxide, water vapor and sensible heat exchanges of a grain sorghum canopy. Boundary Layer Meteorology, 34, 317–331.CrossRefGoogle Scholar

Anderson, J.M., Chow, W.S., and Goodchild, D.J. (1988). Thylakoid membrane organization in sun shade acclimation. Australian Journal of Plant Physiology, 15, 11–26.CrossRefGoogle Scholar

Anderson, L.J., Maherali, H., Johnson, H.B., et al. (2001). Gas exchange and photosynthetic acclimation over subambient to elevated CO2 in a C3-C4 grassland. Global Change Biology, 7, 693–707.CrossRefGoogle Scholar

Andersson, A., Keskitalo, J., Sjödin, A., et al. (2004). A transcriptional timetable of autumn senescence. Genome Biology, 5, R24.CrossRefGoogle ScholarPubMed

Andersson, B. and Barber, J. (1996). Mechanisms of photodamage and protein degradation during photoinhibition of photosystem II. In: Advances in Photosynthesis Vol.5: Photosynthesis and the Environment (ed. Baker, N.R.), Kluwer Academic Publishers, Dordrecht, Netherlands, pp. 101–121.Google Scholar

Andrade, J.L. and Nobel, P.S. (1996). Habitat, CO2 uptake and growth for the CAM epiphytic cactus Epiphyllum phyllanthus in a Panamanian tropical forest. Journal of Tropical Ecology, 12, 291–306.CrossRefGoogle Scholar

Andralojc, P.J., Keys, A.J., Kossmann, J., et al. (2002). Elucidating the biosynthesis of 2-carboxyarabinitol 1-phosphate through reduced expression of chloroplastic fructose 1,6-bisphosphate phosphatase and radiotracer studies with 14CO2. Proceedings of National Academy of Sciences of USA, 99, 4742–4747.CrossRefGoogle ScholarPubMed

Andralojc, P.J., Keys, A.J., Martindale, W., et al. (1996). Conversion of Δ-hamamelose into 2-carboxy D-arabinitol and 2-carboxy D-arabinitol 1-phosphate in leaves of Phaseolus vulgaris L. Journal of Biological Chemistry, 271, 26803–26809.CrossRefGoogle ScholarPubMed

Andrews, J.R., Bredenkamp, G.J. and Baker, N.R. (1993). Evaluation of the role of State transitions in determining the efficiency of light utilisation for CO2 assimilation in leaves. Photosynthesis Research, 38, 15–26.CrossRefGoogle ScholarPubMed

Andrews, T.J. and Muller, G.J. (1985). Photosynthetic gas exchange of the mangrove, Rhizophora stylosa, in its natural environment. Oecologia, 65, 449–455.CrossRefGoogle ScholarPubMed

Angelopulos, K., Dichio, B. and Xiloyannis, C. (1996). Inhibition of photosynthesis in olive trees (Olea europaea L.) during water stress and rewatering. Journal of Experimental Botany, 47, 1093–1100.CrossRefGoogle Scholar

Ankele, E., Kindgren, P., Pesquet, E., et al. (2007). In vivo visualisation of Mg-protoporphyrin IX, a coordinator of photosynthetic gene expression in the nucleus and the chloroplast. The Plant Cell, 19, 1964–1979.CrossRefGoogle Scholar

Antlfinger, A.E. and Wendel, L.F. (1997). Reproductive effort and floral photosynthesis in Spiranthes cernua (Orchidaceae). American Journal of Botany, 84, 769–780.CrossRefGoogle Scholar

Apel, K. and Hirt, H. (2004). Reactive oxygen species: Metabolism, oxidative stress and signal transduction. Annual Reviews of Plant Biology, 55, 373–399.CrossRefGoogle ScholarPubMed

Aphalo, P.J. and Jarvis, P.G. (1991). Do stomata respond to relative humidity. Plant, Cell and Environment, 14, 127–132.CrossRefGoogle Scholar

Aphalo, P.J. and Jarvis, P.G. (1993). An analysis of Ball’s empirical model of stomatal conductance. Annals of Botany, 72, 321–327.CrossRefGoogle Scholar

Apostol, S., Szalai, G., Sujbert, L., et al. (2006). Non-invasive monitoring of the light-induced cyclic photosynthetic electron flow during cold hardening in wheat leaves. Zeitschrift für Naturforschung, 61c, 734–740.Google Scholar

Aranda, I., Pardo, F., Gil, L., et al. (2004). Anatomical basis of the change in leaf mass per area and nitrogen investment with relative irradiance within the canopy of eight temperate tree species. Acta Oecologica, 25, 187–195.CrossRefGoogle Scholar

Aranda, I., Pardos, M., Puértolas, J., et al. (2007). Water-use efficiency in cork oak (Quercus suber) is modified by the interaction of water and light availability. Tree Physiology, 27, 671–677.CrossRefGoogle Scholar

Araujo, W.L., Dias, P.C., Moraes, G.A.B.K., et al. (2008). Limitations to photosynthesis in coffee leaves from different canopy positions. Plant Physiology and Biochemistry, 46, 884–890.CrossRefGoogle ScholarPubMed

Araus, J.L. (2004). The problems of sustainable water use in the Mediterranean and research requirements agriculture. Annals of Applied Biology, 144, 259–272.Google Scholar

Araus, J.L., Bort, J., Steduto, P., et al. (2003). Breeding cereals for Mediterranean conditions: ecophysiological clues for biotechnology application. Annals of Applied Biology, 142, 129–141.CrossRefGoogle Scholar

Araus, J.L., Brown, H.R., Febrero, A., et al. (1993). Ear photosynthesis, carbon isotope discrimination and the contribution of respiratory CO2 to differences in grain mass in Durum Wheat. Plant, Cell and Environment, 16, 383–392.CrossRefGoogle Scholar

Araus, J.L., Sánchez, C. and Cabrera-Bosquet, LL. (2010). Is heterosis in maize mediated through better water use?New Phytologist, 187, 392–406.CrossRefGoogle ScholarPubMed

Araus, J.L., Slafer, G.A., Royo, C., et al. (2008). Breeding for yield potential and stress adaptation in cereals. Critical Reviews in Plant Science, 27, 377–412.CrossRefGoogle Scholar

Arbaugh, M., Bytnerowicz, A., Grulke, N., et al. (2003). Photochemical smog effects in mixed conifer forests along a natural gradient of ozone and nitrogen deposition in the San Bernardino Mountains. Environment International, 29, 401–406.CrossRefGoogle ScholarPubMed

Arbona, V., López-Climent, M.F., Pérez-Clemente, R.M., et al. (2009). Maintenance of a high photosynthetic performance is linked to flooding tolerance in citrus. Environmental and Experimental Botany, 66, 135–142.CrossRefGoogle Scholar

Archetti, M. (2009). Classification of hypotheses on the evolution of autumn colours. Oikos, 118, 328–333.CrossRefGoogle Scholar

Archetti, M., Doring, T.F., Hagen, S.B., et al. (2009). Unravelling the evolution of autumn colours: an interdisciplinary approach. Trends Ecology Evolution, 24, 166–173.CrossRefGoogle Scholar

Ares, A., Fownes, J.H. and Sun, W. (2000). Genetic differentiation of intrinsic water-use efficiency in the Hawaiian native Acacia koa. International Journal of Plant Sciences, 161, 909–915.CrossRefGoogle Scholar

Ariana, D., Guyer, D.E. and Shrestha, B. (2006). Integrating multispectral reflectance and fluorescence imaging for defect detection on apples. Computers and Electronics in Agriculture, 50, 148–161.CrossRefGoogle Scholar

Arimura, G.I., Ozawa, R., Nishioka, T., et al. (2002). Herbivore-induced volatiles induce the emission of ethylene in neigbouring lima bean plants. Plant Journal, 29, 87–98.CrossRefGoogle Scholar

Armond, P.A., Björkman, O. and Staehelin, H.A. (1980) Dissociation of supramolecular complexes in chloroplast membranes. A manifestation of heat damage to the photosynthetic apparatus. Biochimica et Biophysica Acta, 601, 433–442.CrossRefGoogle ScholarPubMed

Armstrong, J.K., Williams, K., Huenneke, L.F., et al. (1988). Topographic position effects on growth depression of California Sierra Nevada pines during the 1982–83 El Niño. Arctic and Alpine Research, 20, 352–357.CrossRefGoogle Scholar

Armstrong, W. and Armstrong, J. (2005). Stem photosynthesis not pressurized ventilation is responsible for light-enhanced oxygen supply to submerged roots of alder (Alnus glutinosa). Annals of Botany, 96, 591–612.CrossRefGoogle Scholar

Arneth, A., Niinemets, Ü. and Pressley, S. (2007). Process-based estimates of terrestrial ecosystem isoprene emissions: incorporating the effects of a direct CO2-isoprene interaction. Atmospheric Chemistry and Physics, 7, 31–53.CrossRefGoogle Scholar

Arnon, D.I. (1949). Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiology, 24, 1–15.CrossRefGoogle ScholarPubMed

Arnon, D.I. (1959). Conversion of light into chemical energy in photosynthesis. Nature, 184, 10–21.CrossRefGoogle ScholarPubMed

Aro, E.M., Virgin, I. and Andersson, B. (1993). Photoinhibition of photosystem II. Inactivation, protein damage and turnover. Biochicima et Biophysica Acta. (Bioenegetics), 1143, 113–134.CrossRefGoogle ScholarPubMed

Aronne, G. and De Micco, V. (2001). Seasonal dimorphism in the Mediterranean Cistus incanus L. subsp. incanus. Annals of Botany, 87, 789–794.CrossRefGoogle Scholar

Arp, W.J. (1991). Effects of source-sink relations on photosynthetic acclimation to elevated CO2. Plant Cell and Environment, 14, 869–875.CrossRefGoogle Scholar

Arquero, O., Barranco, D. and Benlloch, M. (2006). Potassium starvation increases stomatal conductance in olive trees. Hortscience, 41, 433–436.Google Scholar

Arulanantham, A., Rao, I. and Terry, N. (1990). Limiting factors in photosynthesis. VI. Regeneration of ribulose 1, 5-bisphosphate limits photosynthesis at low photochemical capacity. Plant Physiology, 93, 1466–1475.CrossRefGoogle ScholarPubMed

Asada, K. (1996). Radical production and scavenging in the chloroplasts. In: Advances in Photosynthesis Vol.5: Photosynthesis and the Environment (ed. Baker, N.R.), Kluwer Academic Publishers, Dordrecht, Netherlands, pp. 123–150.Google Scholar

Asada, K. (1999). The water-water cycle in chloroplasts: scavenging of active oxygen and dissipation of excess photons. Annual Review of Plant Physiology and Plant Molecular Biology, 50, 601–639.CrossRefGoogle Scholar

Asada, K. (2000). The water–water cycle as alternative photon and electron sinks. Philosophical Transactions of the Royal Society of London B, 355, 11419–1432.CrossRefGoogle ScholarPubMed

Aschan, G. and Pfanz, H. (2003). Non-foliar photosynthesis: a strategy of additional carbon acquisition. Flora, 198, 81–97.CrossRefGoogle Scholar

Aschan, G., Pfanz, H., Vodnik, D., et al. (2005). Photosynthetic performance of vegetative and reproductive structures of green hellebore (Helleborus viridis L. agg.). Photosynthetica, 43, 55–64.CrossRefGoogle Scholar

Ashley, D.A. and Boerma, H.R. (1989). Canopy photosynthesis and its association with seed yield in advanced generations of a soybean cross. Crop Science, 29, 1042–1045.CrossRefGoogle Scholar

Ashmore, M.R. (2002). Effects of oxidants at the whole plant and community level. In: Air pollution and Plant Life 2nd edn (eds Bell, J.N.B. and Treshow, M.), John Wiley and Sons, Chichester, USA, pp. 89–118.Google Scholar

Ashmore, M.R. (2005). Assessing the future global impacts of ozone on vegetation. Plant, Cell and Environment, 28, 949–964.CrossRefGoogle Scholar

Asmus, G.L. and Ferraz, L.C.C.B. (2002). Effect of population densities of Heterodera glycines race 3 on leaf area, photosynthesis and yield of soybean. Fitopatologia Brasileira, 27, 273–278.CrossRefGoogle Scholar

Asner, G.P. and Wessman, C.A. (1997). Scaling PAR absorption from the leaf to landscape level in spatially heterogeneous ecosystems. Ecological Modelling, 103, 81–97.CrossRefGoogle Scholar

Asner, G.P., Wessman, C.A., Bateson, A.C., et al. (2000). Impact of tissue, canopy, and landscape factors on the hyperspectral reflectance variability of arid ecosystems. Remote Sensing of Environment, 74, 69–84.CrossRefGoogle Scholar

Asokanthan, P., Johnson, R.W., Griffith, M., et al. (1997). The photosynthetic potential of canola embryos. Physiologia Plantarum, 101, 353–360.CrossRefGoogle Scholar

Athanasiou, K., Dyson, B.C., Webster, R.E. et al. (2010). Dynamic acclimation of photosynthesis increases plant fitness in changing environments. Plant Physiology, 152, 366–373.CrossRefGoogle ScholarPubMed

Atkin, O.K. and Macherel, D. (2009). The crucial role of plant mitochondria in orchestrating drought tolerance. Annals of Botany, 103, 581–597.CrossRefGoogle ScholarPubMed

Atkin, O.K. and Tjoelker, M.G. (2003). Thermal acclimation and the dynamic response of plant respiration to temperature. Trends Plant Science, 8, 343–351.CrossRefGoogle Scholar

Atkin, O.K., Botman, B. and Lambers, H. (1996). The causes of inherently slow growth in alpine plants: an analysis based on the underlying carbon economies of alpine and lowland Poa species. Functional Ecology, 10, 698–707.CrossRefGoogle Scholar

Atkin, O.K., Evans, J.R. and Siebke, K. (1998). Relationship between the inhibition of leaf respiration by light and enhancement of leaf dark respiration following light treatment. Australian Journal of Plant Physiology, 25, 437–443.CrossRefGoogle Scholar

Atkin, O.K., Scheurwater, I. and Pons, T.L. (2006). High thermal acclimation potential of both photosynthesis and respiration in two lowland Plantago species in contrast to an alpine congeneric. Global Change Biology, 12, 500–515.CrossRefGoogle Scholar

Atkin, O.K., Scheurwater, I. and Pons, T.L. (2007). Respiration as a percentage of daily photosynthesis in whole plants is homeostatic at moderate, but not high, growth temperatures. New Phytologist, 174, 367–380.CrossRefGoogle Scholar

Atkin, O.K., Evans, J.R., Ball, M.C., et al. (2000b). Leaf respiration of snow gum in the light and dark. Interactions between temperature and irradiance. Plant Physiology, 122, 915–923.CrossRefGoogle ScholarPubMed

Atkin, O.K., Millar, A.H., Gärdestrom, P., et al. (2000a). Photosynthesis, carbohydrate metabolism and respiration in leaves of higher plants. In: Photosynthesis, Physiology and Metabolism (eds Leegood, R. C., Sharkey, T. D. and von Caemmerer, S.) Kluwer Academic Publisher, London.Google Scholar

Atkins, C.A., Kuo, J., Pate, J.S., et al. (1977). Photosynthetic pod wall of pea (Pisum sativum L.). Distribution of carbon dioxide-fixing enzymes in relation to pod structure. Plant Physiology, 60, 779–786.CrossRefGoogle ScholarPubMed

Attiwill, P.M. and Adams, M.A. (1993). Nutrient cycling in forests. New Phytologist, 124, 561–582.CrossRefGoogle Scholar

Attiwill, P.M. and Clough, B.F. (1980). Carbon dioxide and water vapor exchange in the white mangrove (Avicennia marina). Photosynthetica, 14, 40–47.Google Scholar

Au, S.F. (1969). Internal leaf surface and stomatal abundance in arctic and alpine populations of Oxyria digyna. Ecology, 50, 131–134.CrossRefGoogle Scholar

Aubert, S., Assard, N., Boutin, J.P., et al. (1999). Carbon metabolism in the subantarctic Kerguelen cabbage Pringlea antiscorbutica R.Br.: environmental controls over carbohydrates and proline contents and relation to phenology. Plant Cell and Environment, 22, 243–254.CrossRefGoogle Scholar

Aubert, S., Choler, P., Pratt, J., et al. (2004). Methyl-beta-D-glucopyranoside in higher plants: accumulation and intraccellular localization in Geum montanum L. leaves and in model systems studied by 13C nuclear magnetic resonance. Journal of Experimental Botany, 55, 2179–2189.CrossRefGoogle Scholar

Aubinet, M., Heinesch, B. and Yernaux, M. (2003). Horizontal and vertical CO2 advection in a sloping forest. Boundary Layer Meteorology, 108, 397–417.CrossRefGoogle Scholar

Aubinet, M., Berbigier, P., Bernhofer, Ch., et al. (2005). Comparing CO2 storage and advection conditions at night at different Carboeuroflux sites. Boundary Layer Meteorology, 116, 63–94.CrossRefGoogle Scholar

Aubinet, M., Grelle, A., Ibrom, A., et al. (2000). Estimates of the annual net carbon and water exchange of forests: the EUROFLUX methodology. Advances in Ecological Research, 30, 113–175.CrossRefGoogle Scholar

Augspurger, C.K. and Bartlett, E.A. (2003). Differences in leaf phenology between juvenile and adult trees in a temperate deciduous forest. Tree Physiology, 23, 517–525.CrossRefGoogle Scholar

Augspurger, C.K., Cheeseman, J.M. and Salk, C.F. (2005). Light gains and physiological capacity of understory woody plants during physiological avoidance of canopy shade. Functional Ecology, 19, 537–546.CrossRefGoogle Scholar

Augusti, A. and Schleucher, J. (2007). The ins and outs of stable isotopes in plants. New Phytologist, 174, 473–475.CrossRefGoogle ScholarPubMed

Austin II, J. and Webber, A.N. (2005). Photosynthesis in Arabidopsis thaliana mutants with reduced chloroplast number. Photosynthesis Research, 85, 373–384.Google Scholar

Avenson, T.J., Cruz, J.A., Kanazawa, A., et al. (2005a). Regulating the proton budget of higher plant photosynthesis. Proceedings of the National Academy of Sciences (USA), 102, 9709–9713.CrossRefGoogle ScholarPubMed

Avenson, T.J., Kanazawa, A., Cruz, J.A., et al. (2005b). Integrating the proton circuit into photosynthesis: progress and challenges. Plant, Cell and Environment, 28, 97–109.CrossRefGoogle Scholar

Awramik, S.M. (1992). The oldest records of photosynthesis. Photosynthesis Research, 33, 75–89.CrossRefGoogle ScholarPubMed

Axelrod, D.I. (1966). Origin of deciduous and evergreen habits in temperate forests. Evolution, 20, 1–15.CrossRefGoogle ScholarPubMed

Baas, W.J. (1989). Secondary plant compounds, their ecological significance and consequences for the carbon budget. In: Causes and Consequences of Variation in Growth Rate and Productivity of Higher Plants (ed. Lambers, H.), SPB Academic Publishing, The Hague, pp. 313–340.Google Scholar

Bacelar, E.A., Mountibho-Pereira, J.M., Gonçalves, B.C., et al. (2007). Changes in growth, gas exchange, xylem hydraulic properties and water use efficiency of three olive cultivars under contrasting water availability regimes. Environmental and Experimental Botany, 60, 183–192.CrossRefGoogle Scholar

Bachereau, F., Marigo, G. and Asta, J. (1998). Effect of solar radiation (UV and visible) at high altitude on CAM-cycling and phenolic compound biosynthesis in Sedum album. Physiologia Plantarum, 104, 203–210.CrossRefGoogle Scholar

Bachmann, A., Fernándes-López, J., Ginsburg, J., et al. (1994). Stay green genotypes of Phaseolus vulgaris L.: chloroplast proteins and chlorophyll catabolites during foliar senescence. New Phytologist, 126, 593–600.CrossRefGoogle Scholar

Backhausen, J., Kitzmann, C., Horton, P., et al. (2000). Electron acceptors in isolated intact spinach chloroplasts act hierarchically to prevent over-reduction and competition for electrons. Photosynthesis Research, 64, 1–13.CrossRefGoogle ScholarPubMed

Badeck, F.W. (1995). Intra-leaf gradient of assimilation rate and optimal allocation of canopy nitrogen: a model on the implications of the use of homogeneous assimilation functions. Australian Journal of Plant Physiology, 22, 425–439.CrossRefGoogle Scholar

Badger, M.R. and Collatz, G.J. (1977). Studies on the kinetic mechanism of ribulose-1,5-bisphosphate carboxylase and oxygenase reactions, with particular reference to the effect of temperature on kinetic parameters. Carnegie Institution of Washington Year Book, 76, 355–361.Google Scholar

Badger, M.R., Björkman, O. and Armond, P.A. (1982). An analysis of photosynthetic response and adaptation to temperature in higher plants: temperature acclimation in the desert evergreen Nerium oleander L. Plant, Cell and Environment, 5, 85–99.Google Scholar

Badger, M.R., Sharkey, T.D. and von Caemmerer, S. (1984). The relationship between steady state gas exchange of bean leaves and the levels of carbon-reduction cycle intermediates. Planta, 160, 305–313.CrossRefGoogle ScholarPubMed

Badger, M.R., Spalding, M.H., Leegood, R.C., et al. (2000a). CO2 acquisition, concentration and fixation in cyanobacteria and algae. In: Advances in Photosynthesis, vol. 9: Photosynthesis, Physiology and Metabolism (ed. Leegood, R.C., Sharkey, T.D. and von Caemmerer, S.), Kluwer Academic, Dordrecht, Netherlands, pp. 369–397.Google Scholar

Badger, M.R., von Caemmerer, S., Ruuska, S., et al. (2000b). Electron flow to oxygen in higher plants and algae: rates and control of direct photoreduction (Mehler reaction) and Rubisco oxygenase. Philosophical Transactions of The Royal Society, 355, 1433–1446.CrossRefGoogle ScholarPubMed

Bahn, M., Rodeghiero, M., Anderson, M., et al. (2008). Soil respiration in European grasslands in relation to climate and assimilate supply. Ecosystems, 11, 1352–1367.CrossRefGoogle ScholarPubMed

Bailey Serres, J. and Voesenek, L.A.C.J. (2008). Flooding stress: acclimations and genetic diversity. Annual Review of Plant Biology, 59, 313–339.CrossRefGoogle ScholarPubMed

Baker, J.T., Kimb, S.H., Gitz, D.C., et al. (2004). A method for estimating carbon dioxide leakage rates in controlled-environment chambers using nitrous oxide. Environmental Experimental Botany, 51, 103–110.CrossRefGoogle Scholar

Baker, J.T., Van Pelt, S., Gitz, D.C., et al. (2009). Canopy gas exchange measurements of cotton in an open system. Agronomy Journal, 101, 52–59.CrossRefGoogle Scholar

Baker, N.R. (2008). Chlorophyll fluorescence: a probe of photosynthesis in vivo. Annual Reviews of Plant Biology, 59, 89–113.CrossRefGoogle ScholarPubMed

Baker, N.R. and Ort, D.R. (1992). Light and crop photosynthetic performance. In Topics in Photosynthesis. Crop Photosynthesis: Spatial and Temporal Determinants. (ed. Baker, N.R. and Thomas, H.), Elsevier, UK, pp. 289–312.Google Scholar

Baker, N.R. and Rosenqvist, E. (2004). Applications of chlorophyll fluorescence can improve crop production strategies: an examination of future possibilities. Journal of Experimental Botany, 55, 1607–1621.CrossRefGoogle ScholarPubMed

Baker, N.R., Harbinson, J. and Kramer, D.M. (2007). Determining the limitations and regulation of photosynthetic energy transduction in leaves. Plant, Cell and Environment, 30, 1107–1125.CrossRefGoogle ScholarPubMed

Baker, N.R., Oxborough, K., Lawson, T., et al. (2001). High resolution imaging of photosynthetic activities of tissues, cells and chloroplasts in leaves. Journal of Experimental Botany, 52, 615–621.CrossRefGoogle ScholarPubMed

Balachandran, S. and Osmond, C.B. (1994). Susceptibility of tobacco leaves to photoinhibition following infection with two strains of tobacco mosaic virus under different light and nitrogen nutrition regimes. Plant Physiology, 104, 1051–1057.CrossRefGoogle ScholarPubMed

Balachandran, S., Hurry, V.M., Kelley, S.E., et al. (1997). Concepts of plant biotic stress: some insights into the stress physiology of virus-infected plants, from the perspective of photosynthesis. Physiologia Plantarum, 100, 203–213.CrossRefGoogle Scholar

Balaguer, L., Manrique, E., de los Rios, A., et al. (1999). Long-term responses of the green-algal lichen Parmelia caperata to natural CO2 enrichment. Oecologia, 119, 166–174.CrossRefGoogle ScholarPubMed

Balaguer, L., Pugnaire, F. I., Martínez-Ferri, E., et al. (2002). Ecophysiological significance of chlorophyll loss and reduced photochemical efficiency under extreme aridity in Stipa tenacissima L. Plant and Soil, 240, 343–352.CrossRefGoogle Scholar

Baldocchi, D. (1994). An analytical solution for coupled leaf photosynthesis and stomatal conductance models. Tree Physiology, 14, 1069–1079.CrossRefGoogle ScholarPubMed

Baldocchi, D. (2003). Assessing the eddy covariance technique for evaluating carbon dioxide exchange rates of ecosystems: past, present and future. Global Change Biology, 9, 479–492.CrossRefGoogle Scholar

Baldocchi, D. and Collineau, S. (1994). The physical nature of solar radiation in heterogeneous canopies: spatial and temporal attributes. In: Exploitation of Environmental Heterogeneity by Plants (eds Caldwell, M.M. and Pearcy, R.W.), Academic Press, San Diego, California, pp. 21–71.Google Scholar

Baldocchi, D.D. (1993). Scaling water vapour and carbon dioxide exchanges from leaves to canopy: rules and tool. In: Scaling Physiological Processes: Leaf to Global (eds Ehleringer, J.R. and Field, C.B.), Academic Press, San Diego, USA, pp. 77–114.Google Scholar

Baldocchi, D.D. (2008). ‘Breathing’ of the terrestrial biosphere: lessons learned from a global network of carbon dioxide flux measurement systems. Australian Journal of Botany, 56, 1–26.CrossRefGoogle Scholar

Baldocchi, D.D. and Amthor, J.S. (2001). Canopy photosynthesis: history, measurements, and models. In: Terrestrial Global Productivity: Past, Present, and Future (eds Mooney, H.A., Saugier, B. and Roy, J.), Academic Press, Inc, San Diego. pp. 9–31.Google Scholar

Baldocchi, D.D. and Harley, P.C. (1995). Scaling carbon dioxide and water vapour exchange from leaf to canopy in a deciduous forest. II. Model testing and application. Plant Cell and Environment, 18, 1157–1173.CrossRefGoogle Scholar

Baldocchi, D.D. and Valentini, R. (associated eds.) (1996). Thematic issue: Strategies for monitoring and modelling CO2 and water vapour fluxes over terrestrial ecosystems. Global Change Biology, 2, 159–318.CrossRefGoogle Scholar

Baldocchi, D.D., Wilson, K.B. and Gu, L. (2002). How the environment, canopy structure and canopy physiological functioning influence carbon, water and energy fluxes of a temperate broad-leaved deciduous forest – an assessment with the biophysical model CANOAK. Tree Physiology, 22, 1065–1077.CrossRefGoogle Scholar

Baldocchi, D.D., Xu, L. and Kiang, N.Y. (2004). How plant functional-type, weather, seasonal drought, and soil physical properties alter water and energy fluxes of an oak-grass savanna and an annual grassland. Agricultural and Forest Meteorology, 123, 13–39.CrossRefGoogle Scholar

Baldocchi, D.D., Falge, E., Gu, L., et al. (2001). FLUXNET: a new tool to study the temporal and spatial variability of ecosystem-scale carbon dioxide, water vapor and energy flux densities. Bulletin of the American Meteorological Society, 82, 2415–2434.2.3.CO;2>CrossRefGoogle Scholar

Baldocchi, D.D., Finnigan, J.J., Wilson, K., et al. (2000). On measuring net ecosystem carbon exchange over tall vegetation on complex terrain. Boundary Layer Meteorology, 96, 257–291.CrossRefGoogle Scholar

Baldocchi, D.D., Hicks, B.B. and Meyers, T.P. (1988). Measuring biosphere-atmosphere exchanges of biologically related gases with micrometeorological methods. Ecology, 69, 1331–1340.CrossRefGoogle Scholar

Baldocchi, D.D., Valentini, R., Running, S., et al. (1996). Strategies for measuring and modelling carbon dioxide and water vapour fluxes over terrestrial ecosystems. Global Change Biology, 2, 159–168.CrossRefGoogle Scholar

Baldwin, A., Egnotovich, M., Ford, M., et al. (2001). Regeneration in fringe mangrove forests damaged by Hurricane Andrew. Plant Ecology, 157, 149–162.CrossRefGoogle Scholar

Baldwin, I.T. (2001). An ecologically motivated analysis of plant-herbivore interactions in native tobacco. Plant Physiology, 127, 1449–1458.CrossRefGoogle ScholarPubMed

Baldwin, I.T. and Callahan, P. (1993). Autotoxicity and chemical defense: nicotine accumulation and carbon gain in solanaceous plants. Oecologia, 94, 534–541.CrossRefGoogle ScholarPubMed

Ball, J.T., Woodrow, I.E. and Berry, J.A. (1987). A model predicting stomatal conductance and its contribution to the control of photosynthesis under different environmental conditions. In: Progress in Photosynthesis Research, Vol. IV (ed. Biggins, I.), Martinus-Nijhoff Publishers, Dordrecht, Netherlands, pp. 221–224.Google Scholar

Ball, M.C. (2002). Interactive effects of salinity and irradiance on growth: implications for mangrove forest structure along salinity gradients. Trees, 16, 126–139.CrossRefGoogle Scholar

Ball, M.C. and Critchley, C. (1982). Photosynthetic responses to irradiance by the grey mangrove, Avicennia marina, grown under different light regimes. Plant Physiology, 70, 1101–1106.CrossRefGoogle ScholarPubMed

Ballare, C.L., Scopel, A.L., Stapleton, A.E., et al. (1996). Solar ultraviolet-B radiation affects seedling emergence, DNA integrity, plant morphology, growth rate, and attractiveness to herbivore insects in Datura ferox. Plant Physiology, 112, 161–170.CrossRefGoogle ScholarPubMed

Baltzer, J.L. and Thomas, S.C. (2007a). Determinants of whole-plant light requirements in Bornean rain forest tree saplings. Journal of Ecology, 95, 1208–1221.CrossRefGoogle Scholar

Baltzer, J.L. and Thomas, S.C. (2007b). Physiological and morphological correlates of whole-plant light compensation point in temperate deciduous tree seedlings. Oecologia, 153, 209–223.CrossRefGoogle ScholarPubMed

Baltzer, J.L., Davies, S.J., Bunyavejchewin, S., et al. (2008). The role of desiccation tolerance in determining tree species distributions along the Malay Thai Peninsula. Functional Ecology, 22, 221–231.CrossRefGoogle Scholar

Baltzer, J.L., Thomas, S.C., Nilus, R., et al. (2005). Edaphic specialization in tropical trees: physiological correlates and responses to reciprocal transplantation. Ecology, 86, 3063–3077.CrossRefGoogle Scholar

Bansal, S. and Germino, M.J. (2008). Carbon balance of conifer seedlings at timberline: relative changes in uptake, storage, and utilization. Oecologia, 158, 217–227.CrossRefGoogle ScholarPubMed

Barak, P. and Helmke, P.A. (1993). The chemistry of zinc. In: Zinc in Soils and Plants, Developments in Plants and Soil Sciences (ed. Robson, A). Kluwer Academic Press, New York, USA, pp. 1–13.Google Scholar

Barbehenn, R.V., Karowe, D.N. and Zhong, C. (2004).Performance of a generalist grasshopper on a C3 and a C4 grass: compensation for the effects of elevated CO2 on plant nutritional quality. Oecologia, 140, 96–103.CrossRefGoogle Scholar

Barber, J. (2008a). Photosynthetic generation of oxygen. Philosophical Transactions of the Royal Society B, 363, 2665–2674.CrossRefGoogle ScholarPubMed

Barber, J. (2008b). Crystal structure of the oxygen-evolving complex of Photosystem II. Inorganic Chemistry, 47, 1700–1710.CrossRefGoogle ScholarPubMed

Barbour, M.M. (2007). Stable oxygen isotope composition of plant tissue: a review. Functional Plant Biology, 34, 83–94.CrossRefGoogle Scholar

Barbour, M.M. and Buckley, T.N. (2007). The stomatal response to evaporative demand persists at night in Ricinus communis plants with high nocturnal conductance. Plant, Cell and Environment, 30, 711–721.CrossRefGoogle ScholarPubMed

Barbour, M.M. and Farquhar, G.D. (2000). Relative humidity and ABA-induced variation in carbon and oxygen isotope ratios of cotton leaves. Plant, Cell and Environment, 23, 473–485.CrossRefGoogle Scholar

Barbour, M.M., Cernusak, L.A. and Farquhar, G.D. (2005). Factors affecting the oxygen isotope ratio of plant organic material. In: Stable Isotopes and Biosphere-Atmosphere Interactions (eds Flanagan, L.B., Ehleringer, J.R. and Pataki, D.E.), Elsevier Academic Press, San Diego, pp. 9–28.Google Scholar

Barbour, M.M., Fischer, R.A., Sayre, K.D., et al. (2000b). Oxygen isotope ratio of leaf and grain material correlates with stomatal conductance and grain yield in irrigated wheat. Australian Journal of Plant Physiology, 27, 625–637.Google Scholar

Barbour, M.M., McDowell, N.G., Tcherkez, G., et al. (2007). A new measurement technique reveals rapid post-illumination changes in the carbon isotope composition of leaf-respired CO2. Plant, Cell and Environment, 30, 469–482.CrossRefGoogle ScholarPubMed

Barbour, M.M., Shurr, U., Henry, B.K., et al. (2000a). Variation in the oxygen isotope ratio of phloem sap sucrose from castor bean: evidence in support of the Péclet effect. Plant Physiology, 123, 671–679.CrossRefGoogle ScholarPubMed

Barbour, M.M., Warren, C.R., Farquhar, G.D., et al. (2010). Variability in mesophyll conductance between barley genotypes, and effects on transpiration efficiency and carbon isotope discrimination. Plant, Cell and Environment, 33, 1176–1185.Google ScholarPubMed

Bar-Even, A., Noor, E., Lewis, N.E., et al. (2010). Design and analysis of synthetic carbon fixation pathways. Proceedings of the National Academy of Sciences USA, 107, 8889–8894.CrossRefGoogle ScholarPubMed

Bariac, T., Gonzales-Dunia, J., Tardieu, F., et al. (1994). Spatial variation of the isotopic composition of water (18O, 2H) in organs of aerophytic plants. 1. Assessment under laboratory conditions. Chemical Geology, 115, 307–315.CrossRefGoogle Scholar

Barker, D.A., Seaton, G.G.R. and Robinson, S.A. (1997). Internal and external photoprotection in developing leaves of the CAM plant Cotyledon orbiculata. Plant Cell and Environment, 20, 617–624.CrossRefGoogle Scholar

Barker, D.H., Vanier, C., Naumburg, E., et al. (2006). Enhanced monsoon precipitation and nitrogen deposition affect leaf traits and photosynthesis differently in spring and summer in the desert shrub Larrea tridentata. New Phytologist, 169, 799–808.CrossRefGoogle ScholarPubMed

Barker, E.R., Press, M.C., Scholes, J.D., et al. (1996). Interactions between the parasitic angiosperm Orobanche aegyptiaca and its tomato host: growth and biomass allocation. New Phytologist, 133, 637–642.CrossRefGoogle Scholar

Barnes, B.B., Zak, D.R., Denton, S.R., et al. (1998). Forest Ecology, 4th edn. John Wiley and Sons Inc., New York, USA.Google Scholar

Barnes, J., Davison, A., Balaguer, L., et al. (2007). Resistance to air pollutants: from cell to community. In: Functional Plant Ecology (eds Pugnaire, F.I. and Valladares, F.) 2nd edn: CRC Press, USA, pp. 601–626.Google Scholar

Barnes, P.W. and Archer, S. (1996). Influence of an overstorey tree (Prosopis glandulosa) on associated shrubs in a savanna parkland: implications for patch dynamics. Oecologia, 105, 493–500.CrossRefGoogle Scholar

Baroli, I. and Niyogi, K.K. (2000). Molecular genetics of xanthophyll-dependent photoprotection in green algae and plants. Philosophical Transactions of the Royal Society B, 355, 1385–1394.CrossRefGoogle ScholarPubMed

Baroli, I., Price, G.D., Badger, M.R., et al. (2008). The contribution of photosynthesis to the red light response of stomatal conductance. Plant Physiology, 146, 737–747.CrossRefGoogle ScholarPubMed

Barón, M., Arellano, J.B. and López Gorgé, J. (1995). Copper and photosystem II: a controversial relationship. Physiologia Plantarum, 94, 174–180.CrossRefGoogle Scholar

Barrantes, O., Moliner, E., Plaza, M., et al. (1997). Preliminary results of an SO2 experiment with Pinus halepensis Mill. seedlings in open top chambers. In: Impact of Global Change on Tree Physiology and Forest Ecosystems (eds Mohren, G.M.J., Kramer, K. and Sabaté, S.), Kluwer Academic Publishers, Dordrecht, Netherlands, pp. 111–118.Google Scholar

Barry, J.C., Morgan, M.E., Flynn, L.J., et al. (2002). Faunal and environmental change in the late Miocene Siwaliks of northern Pakistan. Paleobiology Memoirs, 28, 1–55.CrossRefGoogle Scholar

Barry, R.G. (2008). Mountain, weather and climate. 3rd edn. Cambridge University Press, Cambridge, UK.

Barta, C. and Loreto, F. (2006). The relationship between the methyl-erythritol phosphate pathway leading to emission of volatile isoprenoids and abscisic acid content in leaves. Plant Physiology, 141, 1676–1683.CrossRefGoogle ScholarPubMed

Barták, M., Gloser, J. and Hájek, J. (2005). Visualized photosynthetic characteristics of the lichen Xanthoria elegans related to daily courses of light, temperature and hydration: a field study from Galindez Island, maritime Antarctica. Lichenologist, 37, 433–443.CrossRefGoogle Scholar

Barták, M.L., Váczi, P., Hájek, J., et al. (2006). Low-temperature limitation of primary photosynthetic processes in Antarctic lichens Umbilicaria antarctica and Xanthoria elegans. Polar Biology, 31, 47–51.CrossRefGoogle Scholar

Bartelink, H.H. (1998). A model of dry matter partitioning in trees. Tree Physiology, 18, 91–101.CrossRefGoogle ScholarPubMed

Bartels, D. and Salamini, F. (2001). Desiccation tolerance in the resurrection plant Craterostigma plantagineum: a contribution to the study of drought tolerance at the molecular level. Plant Physiology, 127, 1346–1353.CrossRefGoogle Scholar

Bartoli, C.G., Gómez, F., Gergoff, G., et al. (2005). Up-regulation of the mitochondrial alternative oxidase pathway enhances photosynthetic electron transport under drought conditions. Journal of Experimental Botany, 56, 1269–1276.CrossRefGoogle ScholarPubMed

Barton, A.M., Fetcher, N. and Redhead, S. (1989). The relationship between treefall gap size and light-flux in a Neotropical rain-forest in Costa-Rica. Journal of Tropical Ecology, 5, 437–439.CrossRefGoogle Scholar

Baruch, Z. and Bilbao, B. (1999). Effects of fire and defoliation on the life history of native and invader C-4 grasses in a Neotropical savanna. Oecologia, 119, 510–520.CrossRefGoogle Scholar

Basak, U.C., Das, A.B. and Das, P. (1996). Chlorophylls, carotenoids, proteins and secondary metabolites in leaves of 14 species of mangrove. Bulletin of Marine Science, 58, 654–659.Google Scholar

Basha, E., Lee, G.J., Breci, L.A., et al. (2004). The identity of proteins associated with a small heat shock protein during heat stress in vivo indicates that these chaperones protect a wide range of cellular functions. Journal of Biological Chemistry, 279, 7566–7575.CrossRefGoogle ScholarPubMed

Basile, B., Reidel, E.J., Weinbaum, S.A., et al. (2003). Leaf potassium concentration, CO2 exchange and light interception in almond trees (Prunus dulcis (Mill) D.A. Webb). Scientia Horticulturae, 98, 185–194.CrossRefGoogle Scholar

Bassham, J.A. and Calvin, M. (1957). The Path of Carbon in Photosynthesis. Prentice-Hall, N.J., USA, p. 104.Google Scholar

Baszynski, T., Wajda, L., Krol, M., et al. (1980). Photosynthetic activities of cadmium-treated tomato plants. Physiologia Plantarum, 48, 365–370.CrossRefGoogle Scholar

Bauer, H., Nagele, M., Comploj, M., et al. (1994). Photosynthesis in cold-acclimated leaves of plants with various degrees of freezing tolerance. Physiologia Plantarum, 91, 403–412.CrossRefGoogle Scholar

Bauerle, W.L., Hinckley, T.M., Chermák, J., et al. (1999). The canopy water relations of old-growth Douglas-fir trees. Trees, 13, 211–217.CrossRefGoogle Scholar

Baxter, C.J., Redestig, H., Schauer, N., et al. (2007). The metabolic response of heterotrophic Arabidopsis cells to oxidative stress. Plant Physiology, 143, 312–325.CrossRefGoogle ScholarPubMed

Bazzaz, F.A., Carlson, R.W. and Harper, J.L. (1979). Contribution to reproductive effort by photosynthesis of flowers and fruits. Nature, 279, 554–555.CrossRefGoogle Scholar

Beadle, N.C.W. (1966). Soil phosphate and its role in molding segments of the Australian flora and vegetation with special reference to xeromorphy and sclerophylly. Ecology, 47, 992–1007.CrossRefGoogle Scholar

Bean, R.C., Porter, G.G. and Barr, K.B. (1963). Photosynthesis and respiration in developing fruits. III. Variations in photosynthesis capacity during colour change. Plant Physiology, 38, 285–290.CrossRefGoogle Scholar

Beauchamp, J., Wisthaler, A., Hansel, A., et al. (2005). Ozone induced emissions of biogenic VOC from tobacco: relations between ozone uptake and emission of LOX products. Plant, Cell and Environment, 28, 1334–1343.CrossRefGoogle Scholar

Beauford, W., Barber, J. and Barringer, A.R. (1977). Uptake and distribution of mercury within higher plants. Physiologia Plantarum, 39, 261–265.CrossRefGoogle Scholar

Becher, M., Talke, I.N., Krall, L., et al. (2004). Cross-species microarray transcript profiling reveals high constitutive expression of metal homeostasis genes in shoots of the zinc hyperaccumulator Arabidopsis halleri. Plant Journal, 37, 251–268.CrossRefGoogle ScholarPubMed

Beck, C. (2005). Signaling pathways from the chloroplast to the nucleus. Planta, 222, 743–756.CrossRefGoogle ScholarPubMed

Beck, E., Senser, M., Scheibe, R., et al. (1982). Frost avoidance and freezing tolerance in Afroalpine ‘giant rosette’ plants. Plant Cell and Environment, 5, 215–222.Google Scholar

Bednarz, C.W. and van Iersel, M.W. (1999). Continuous whole plant carbon dioxide exchange rates in cotton treated with pyrithiobac. The Journal of Cotton Science, 3, 53–59.Google Scholar

Bednarz, C.W. and van Iersel, M.W. (2001). Temperature response of whole-plant CO2 exchange rates of four upland cotton cultivars differing in leaf shape and leaf pubescence. Communications in Soil Science and Plant Analysis, 32, 2485–2501.CrossRefGoogle Scholar

Beer, C., Ciais, P., Reichstein, M., et al. (2009). Temporal and among-site variability of inherent water use efficiency at the ecosystem level. Global Biogeochemical Cycles, 23, GB2018.CrossRefGoogle Scholar

Beer, C., Reichstein, M., Ciais, P., et al. (2007). Mean annual GPP of Europe derived from its water balance. Geophysical Research Letters, 34, L05401.CrossRefGoogle Scholar

Beer, C., Reichstein, M., Tomelleri, E. et al. (2010). Terrestrial gross carbon dioxide uptake: global distribution and covariation with climate. Science, 329, 834–838.CrossRefGoogle ScholarPubMed

Beerling, D.J. (2005). Leaf evolution: gases, genes and geochemistry. Annals of Botany, 96, 345–352.CrossRefGoogle ScholarPubMed

Beerling, D.J. and Kelly, C.K. (1996). Evolutionary comparative analyses of the relationship between leaf structure and function. The New Phytologist, 134, 35–51.CrossRefGoogle Scholar

Beerling, D.J. and Osborne, C.P. (2006). The origin of the savanna biome. Global Change Biology, 12, 2023–2031.CrossRefGoogle Scholar

Beerling, D.J. and Rundgren, M. (2000). Leaf metabolic and morphological responses of dwarf willow (Salix herbacea) in the Sub-Arctic to the past 9000 years of global environmental change. New Phytologist, 145, 257–269.CrossRefGoogle Scholar

Beerling, D.J. and Woodward, F.I. (1996). Paleo-ecophysiological perspectives on plant responses to global change. Trends in Ecology and Evolution, 11, 20–23.CrossRefGoogle ScholarPubMed

Beerling, D.J. and Woodward, F.I. (1997). Changes in land plant function over the Phanerozoic: recontructions based on the fossil record. Botanical Journal of the Linnean Society, 124, 137–153.CrossRefGoogle Scholar

Beerling, D.J. and Woodward, F.I. (2001). Vegetation and the Terrestrial Carbon Cycle: Modelling the First 400 Million Years. Cambridge University Press,Cambridge, UK.CrossRefGoogle Scholar

Beerling, D.J., McElwain, J.C. and 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.Google Scholar

Beerling, D.J., Osborne, C.P., Chaloner, W.G. (2001). Evolution of leaf-form in land plants linked to atmospheric CO2 decline in the Late Paleozoic era. Nature, 410, 352–354.CrossRefGoogle Scholar

Behrensmeyer, A.K., Quade, J., Cerling, T.E., et al. (2007). The structure and rate of late Miocene expansion of C4 plants: evidence from lateral variation in stable isotopes in paleosols of the Siwalik Group, northern Pakistan. Geological Society of America Bulletin, 119, 1486–1505.CrossRefGoogle Scholar

Belkhodja, R., Morales, F., Quílez, R., et al. (1998). Iron deficiency causes changes in chlorophyll fluorescence due to the reduction in the dark of the photosystem II acceptor side. Photosynthesis Research, 56, 265–276.CrossRefGoogle Scholar

Bellingham, P.J., Kohyama, T. and Aiba, S.I. (1996). The effects of a typhoon on Japanese warm temperate rainforests. Ecological Research, 11, 229–247.CrossRefGoogle Scholar

Belsky, A.J., Amundson, R.G.Duxbury, J.M. et al. (1989). The effects of trees on their physical, chemical, and biological environments in a semi-arid savanna in Kenya. Journal of Applied Ecology, 26, 1005–1024.CrossRefGoogle Scholar

Bendall, D.S. and Manasse, R.S. (1995). Cyclic photophosphorylation and electron transport. Biophysica et Biochimica Acta (Bioenergetics), 1229, 23–38.CrossRefGoogle Scholar

Bender, M., Sowers, T. and Labeyrie, L. (1994). The Dole effect and its variations during the last 130,000 years as measured in the Vostok ice core. Global Biogeochemical Cycles, 8, 363–376.CrossRefGoogle Scholar

Bender, M.M. (1968). Mass spectrometric studies of carbon-13 variations in corn and other grasses. Radiocarbon, 10, 468–472.CrossRefGoogle Scholar

Bender, M.M. (1971). Variations in the 13C/12C ratios of plants in relations to the pathway of photosynthetic carbon dioxide fixation. Phytochemistry, 10, 1239–1244.CrossRefGoogle Scholar

Bender, M.M., Rouhani, I., Vines, H.M., et al. (1973). 13C/12C ratio changes in crassulacean acid metabolism plants. Plant Phisiology, 52, 427–430.CrossRefGoogle Scholar

Benkeblia, N., Shinano, T. and Osaki, M. (2007). Metabolite profiling and assessment of metabolome compartmentation of soybean leaves using non-aqueous fractionation and GC-MS analysis. Metabolomics, 2, 297–305.CrossRefGoogle Scholar

Bennoun, P. (2001). Chlororespiration and the process of carotenoid biosynthesis. Biochimica et Biophysica Acta – Bioenergetics, 1506, 133–142.CrossRefGoogle ScholarPubMed

Benowicz, A., Guy, R.D. and El-Kassaby, Y.A. (2000). Geographic pattern of genetic variation in photosynthetic capacity and growth in two hardwood species from British Columbia. Oecologia, 123, 168–174.CrossRefGoogle ScholarPubMed

Benzing, D.H. (1990). Vascular Epiphytes: General Biology and Related Biota. Cambridge University Press, Cambridge, UK.CrossRefGoogle Scholar

Berard, R.G. and Thurtell, G.W. (1990). Respiration measurements of maize plants using a whole-plant enclosure system. Agronomy Journal, 82, 641–643.CrossRefGoogle Scholar

Berenbaum, M.R. and Zangerl, A.R. (2008). Facing the future of plant-insect interaction research: le retour a la “raison d’etre”. Plant Physiology, 146, 804–811.CrossRefGoogle ScholarPubMed

Berger, B., Parent, B. and Tester, M. (2010). High-throughput shoot imaging to study drought responses. Journal of Experimental Botany, 61, 3519–3528.CrossRefGoogle ScholarPubMed

Berger, S., Benediktyová, Z., Matouš, K., et al. (2007). Visualization of dynamics of plant-pathogen interaction by novel combination of chlorophyll fluorescence imaging and statistical analysis: differential effects of virulent an avirulent strains of P. syringae and of oxylipins on A. thaliana. Journal of Experimental Botany, 58, 797–806.CrossRefGoogle ScholarPubMed

Berger, S., Papadopoulos, M., Schreiber, U., et al. (2004). Complex regulation of gene expression, photosynthesis and sugar levels by pathogen infection in tomato. Physiologia Plantarum, 122, 419–428.CrossRefGoogle Scholar

Beringer, J., Hutley, L.B., Tapper, N.J., et al. (2007). Savanna fires and their impact on net ecosystem productivity in North Australia. Global Change Biology, 13, 990–1004.CrossRefGoogle Scholar

Bernacchi, C.J., Calfapietra, C., Davey, P.A., et al. (2003b). Photosynthesis and stomatal conductance responses of poplars to free-air CO2 enrichment (PopFACE) during the first growth cycle and immediately following coppice. New Phytologist, 159, 609–621.CrossRefGoogle Scholar

Bernacchi, C.J., Hollinger, S.E. and Meyers, T. (2005b). The conversion of the corn/soybean ecosystem to no-till agriculture may result in a carbon sink. Global Change Biology, 11, 1867–1872.Google Scholar

Bernacchi, C.J., Kimball, B., Quarles, D., et al. (2007). Decreases in stomatal conductance of soybean under open-air elevation of [CO2] are closely coupled with decreases in ecosystem evapotranspiration. Plant Physiology, 143, 134–144.CrossRefGoogle Scholar

Bernacchi, C.J., Leakey, A.D.B., Heady, L.E., et al. (2006). Hourly and seasonal variation in photosynthesis and stomatal conductance of soybean grown at future CO2 and ozone concentrations for 3 years under fully open-air field conditions. Plant, Cell and Environment, 29, 2077–2090.CrossRefGoogle Scholar

Bernacchi, C.J., Morgan, P.B., Ort, D.R., et al. (2005a). The growth of soybean under free air [CO2] enrichment (FACE) stimulates photosynthesis while decreasing in vivo Rubisco capacity. Planta, 220, 434–446.CrossRefGoogle ScholarPubMed

Bernacchi, C.J., Pimentel, C. and Long, S.P. (2003a). In vivo temperature response functions of parameters required to model RuBP-limited photosynthesis. Plant, Cell and Environment, 26, 1419–1430.CrossRefGoogle Scholar

Bernacchi, C.J., Portis, A.R., Nakano, H., et al. (2002). Temperature response of mesophyll conductance: implications for the determination of Rubisco enzyme kinetics and for limitations to photosynthesis in vivo. Plant Physiology, 130, 1992–1998.CrossRefGoogle ScholarPubMed

Bernacchi, C.J., Singsaas, E.L., Pimentel, C., et al. (2001). Improved temperature response functions for models of Rubisco-limited photosynthesis. Plant Cell and Environment, 24, 253–259.CrossRefGoogle Scholar

Berner, R.A. (1990). Atmospheric carbon dioxide levels over phanerozoic time. Science, 249, 1382–1386.CrossRefGoogle ScholarPubMed

Berner, R.A. and Canfield, D.E. (1989). A new model for atmospheric oxygen over phaenerozoic time. American Journal of Science, 289, 333–361.CrossRefGoogle ScholarPubMed

Berni, J.A., Zarco-Tejada, P.J., Suarez, L., et al. (2009). Thermal and narrowband multispectral remote sensing for vegetation monitoring from an unmanned aerial vehicle. IEEE Transactions on Geoscience and Remote Sensing, 47, 722–738.CrossRefGoogle Scholar

Berninger, F. (1997). Effects of drought and phenology on GPP a simulation study along a geographical gradient. Functional Ecology, 11, 33–42.CrossRefGoogle Scholar

Berova, M., Stoeva, N., Zlatev, Z., et al. (2007). Physiological changes in bean (Phaseolus vulgaris L.) leaves, infected by the most important bean diseases. Journal of Central European Agriculture, 8, 57–62.Google Scholar

Berry, J.A. and Björkman, O. (1980). Photosynthetic response and adaptation to temperature in higher plants. Annual Review of Plant Physiology, 31, 491–543.CrossRefGoogle Scholar

Bertamini, M., Muthuchelian, K. and Nedunchezhian, N. (2004). Effect of grapevine leafroll on the photosynthesis of field grown grapevine plants (Vitis vinifera L. cv. Lagrein). Journal of Phytopathology, 152, 145–152.CrossRefGoogle Scholar

Bertone, P. and Snyder, M. (2007). Prospects and challenges in proteomics. Plant Physiology, 138, 560–562.CrossRefGoogle Scholar

Bertsch, W.F. and Azzi, J.R. (1965). A relative maximum in the decay of long-term delayed light emission from the photosynthetic apparatus. Biochimica et Biophysica Acta, 94, 15–26.CrossRefGoogle ScholarPubMed

Berveiller, D., Kierzkowski, D. and Damesin, C. (2007a). Interspecific variability of stem photosynthesis among tree species. Tree Physiology, 27, 53–61.CrossRefGoogle ScholarPubMed

Berveiller, D., Vidal, J., Degrouard, J., et al. (2007b). Tree stem phosphoenolpyruvate carboxylase (PEPC): lack of biochemical and localization evidence for a C4-like photosynthesis system. New Phytologist, 176, 775–781.CrossRefGoogle ScholarPubMed

Besson-Bard, A., Pugin, A. and Wendehenne, D. (2008). New insights into nitric oxide signaling in plants. Annual Review of Plant Biology, 59, 21–39.CrossRefGoogle ScholarPubMed

Betts, R.A., Boucher, O., Collins, M., et al. (2007). Projected increase in continental runoff due to plant responses to increasing carbon dioxide. Nature, 448, 1037–1041.CrossRefGoogle ScholarPubMed

Betzelberger, A.M., Gillespie, K.M., McGrath, J.M., et al. (2010). Effects of chronic elevated ozone concentration on antioxidant capacity, photosynthesis and seed yield of 10 soybean cultivars. Plant, Cell and Environment, 33, 1569–1581.Google ScholarPubMed

Beuker, E. (1994). Adaptations to climate change of the timing of bud burst of Pinus sylvestris L. And Picea abies Karst. Trees, 14, 961–970.Google Scholar

Beyschlag, W., Kresse, F., Ryel, R.J., et al. (1994). Stomatal patchiness in conifers: experiments with Picea abies (L.) Karst. and Abies alba Mill. Trees: Structure and Function, 8, 132–138.CrossRefGoogle Scholar

Beyschlag, W., Pfanz, H. and Ryel, R.J. (1992). Stomatal patchiness in Mediterranean evergreen sclerophylls. Phenomenology and consequences for the interpretation of the midday depression in photosynthesis and transpiration. Planta, 187, 546–553.CrossRefGoogle ScholarPubMed

Bickford, C.P., Hanson, D.T. and McDowell, N.G. (2010). Influence of diurnal variation in mesophyll conductance on modeled 13C discrimination: results from a field study. Journal of Experimental Botany, 61, 3223–3233.CrossRefGoogle Scholar

Bickford, C.P., McDowell, N.G., Erhardt, E.B., et al. (2009). High-frequency field measurements of diurnal carbon isotope discrimination and internal conductance in a semi-arid species, Juniperus monosperma. Plant, Cell and Environment, 32, 796–810.CrossRefGoogle Scholar

Bieleski, R.L. (1973). Phosphate pools, phosphate transport, and phosphate availability. Annual Review of Plant Physiology, 24, 225–252.CrossRefGoogle Scholar

Bigras, F.J. and Bertrand, A. (2006). Responses of Picea mariana to elevated CO2 concentration during growth, cold hardening and dehardening: phenology, cold tolerance, photosynthesis and growth. Tree Physiology, 26, 875–888.CrossRefGoogle Scholar

Bilger, H.W., Schreiber, U. and Lange, O.L. (1984). Determination of leaf heat resistance: comparative investigation of chlorophyll fluorescence changes and tissue necrosis methods. Oecologia, 63, 256–262.CrossRefGoogle Scholar

Bilger, W. and Björkman, O. (1991). Temperature dependence of violaxanthin de-epoxidation and non-photochemical fluorescence quenching in intact leaves of Gossypium hirsutum L. and Malva parviflora L. Planta, 184, 226–234.CrossRefGoogle ScholarPubMed

Bilger, W., Björkmann, O. and Thayer, S.S. (1989). Light-induced spectral absorbance changes in relation to photosynthesis and the epoxidation state of xanthophyll cycle components in cotton leaves. Plant Physiology, 91, 542–551.CrossRefGoogle ScholarPubMed

Bilger, W., Veit, M., Schreiber, L., et al. (1997). Measurement of leaf epidermal transmittance of UV radiation by chlorophyll fluorescence. Physiologia Plantarum, 101, 754–763.CrossRefGoogle Scholar

Bilgin, D.D., Zavala, J.A., Zhu, J., et al. (2010). Biotic stress globally downregulates photosynthesis genes. Plant, Cell and Environment, 33, 1597–1613.CrossRefGoogle ScholarPubMed

Billesbach, D.P., Fischer, M.L., Torn, M.S., et al. (2004). A portable eddy covariance system for the measurement of ecosystem–atmosphere exchange of CO2, water vapor, and Energy. Journal of Atmospheric and Oceanic Technology, 21, 639–650.2.0.CO;2>CrossRefGoogle Scholar

Billings, W.D. (1973). Arctic and alpine vegetations: similarities, differences and susceptibility to disturbance. BioScience, 37, 58–67.Google Scholar

Billings, W.D. (1974). Adaptations and origins of alpine plants. Arctic and Alpine Research, 6, 129–142.CrossRefGoogle Scholar

Billings, W.D. and Mooney, H.A. (1968). The ecology of arctic and alpine plants. Biological Reviews, 481–529.CrossRefGoogle Scholar

Bird, A.F. (1974). Plant response to root-knot nematode. Annual Review of Phytopathology, 12, 69–85.CrossRefGoogle Scholar

Bird, I.F., Cornelius, M.J. and Keys, A.J. (1982). Affinity of RuBP carboxylases for carbon dioxide and inhibition of the enzymes by oxygen. Journal of Experimental Botany, 33, 1004–1013.CrossRefGoogle Scholar

Birkhold, K.T., Koch, K.E. and Darnell, R.L. (1992). Carbon and nitrogen economy of developing rabbiteye blueberry fruit. Journal of the American Society of Horticultural Sciences, 117, 139–145.Google Scholar

Birth, G.S. and McVey, G.R. (1968). Measuring the colour of growing turf with a reflectance spectrophotometer. Agronomy Journal, 60, 640–643.CrossRefGoogle Scholar

Biswal, B., Smith, A.J. and Rogers, L.J. (1994). Changes in carotenoids but not in D1 protein in response to nitrogen depletion and recovery in a cyanobacterium. FEMS Microbiology Letters, 116, 341–347.CrossRefGoogle Scholar

Biswal, U.C., Biswal, B. and Raval, M.K. (2003). Chloroplast Biogenesis: From Protoplastid to Gerontoplast, Kluwer Academic Publishers, Dordrecht, Netherlands.CrossRefGoogle Scholar

Björkman, O. (1971). Comparative photosynthetic CO2 exchange in higher plants. In: Photosynthesis and Photorespiration (eds Hatch, M.D., Osmond, C.B. and Slatyer, R.O.), Wiley Interscience, New York, USA. pp. 18–32.Google Scholar

Björkman, O. (1981). Responses to different quantum flux densities. In: Physiological Plant Ecology, vol I, Encyclopedia of Plant Physiology, 12A (eds Lange, O.L., Nobel, P.S., Osmond, C.B. and Ziegler, H.), Springer-Verlag, Berlin, pp. 57–107.Google Scholar

Björkman, O. (1994). Responses to long-term drought and high-irradiance stress in natural vegetation. Carnegie Institution of Washington Yearbook, 94, 62–63.Google Scholar

Björkman, O. and Demmig, B. (1987). Photon yield of O2 evolution and chlorophyll fluorescence characteristics at 77K among vascular plants of diverse origins. Planta, 170, 489–504.CrossRefGoogle Scholar

Björkman, O. and Demmig-Adams, B. (1994). Regulation of photosynthetic light energy capture, conversion and dissipation in leaves of higher plants. In: Ecophysiology of Photosynthesis (eds Schulze, E.-D. and Caldwell, M.M.), Springer-Verlag. Berlin. pp. 17–47.Google Scholar

Björkman, O., Badger, M.R. and Armond, P.A. (1980). Response and adaptation of photosynthesis to high temperature. In: Adaptations of Plants to Water and High Temperature Stress (eds Turner, N.C. and Kramer, P.J.), Wiley Interscience, NY, USA, pp. 223–249.Google Scholar

Björkman, O., Pearcy, R.W, Harrison, A.T., et al. (1972). Photosynthetic adaptation to high temperatures: a field study in Death Valley, California. Science, 175, 786–789.CrossRefGoogle ScholarPubMed

Black, C.C. (1973). Photosynthetic carbon fixation in relation to net CO2 uptake. Annual Review of Plant Physiology, 24, 253–286.CrossRefGoogle Scholar

Black, K., Davis, P., McGrath, J., et al. (2005). Interactive effects of irradiance and water availability on the photosynthetic performance of Picea sitchensis seedlings: implications for seedling establishment under different management practices. Annals of Forest Science, 62, 413–422.CrossRefGoogle Scholar

Black, T.A., Gaumont-Guay, D., Jassla, R., et al. (2005). Measurement of CO2 exchange between the boreal forest and the atmosphere. In: The Carbon Balance of Forest Biomes (eds Griffiths, H and Jarvis, P.G., Taylor & Francis, Oxon.Google Scholar

Blackburn, G.A. (2007). Hyperspectral remote sensing of plant pigments. Journal of Experimental Botany, 58, 855–867.CrossRefGoogle ScholarPubMed

Blanke, M.M. (2002). Photosynthesis of strawberry fruit. Acta Horticulturae, 567, 373–376.CrossRefGoogle Scholar

Blanke, M.M. and Cooke, D.T. (2004). Effects of flooding and drought on stomatal activity, transpiration, photosynthesis, water potential and water channel activity in strawberry stolons and leaves. Plant Growth Regulation, 42, 153–160.CrossRefGoogle Scholar

Blanke, M.M. and Lenz, F. (1989). Fruit photosynthesis. Plant, Cell and Environment, 12, 31–46.CrossRefGoogle Scholar

Blankenship, R.E. (1992). Origin and early evolution of photosynthesis. Photosynthesis Research, 33, 91–111.CrossRefGoogle ScholarPubMed

Blankenship, R.E., Tiede, D.M., Barber, J. et al. (2011). Comparing photosynthetic and photovoltaic efficiencies and recognizing the potential for improvement. Science, 332, 805–809.CrossRefGoogle Scholar

Bläsing, O.E., Ernst, K., Streubel, M., et al. (2002). The non-photosynthetic phosphoenolpyruvate carboxylases of the C4 dicot Flaveria trinervia: implications for the evolution of C4 photosynthesis. Planta, 215, 448–456.Google ScholarPubMed

Blasius, B., Neff, R., Beck, F., et al. (1999). Oscillatory model of crassulacean acid metabolism with a dynamic hysteresis switch. Proceedings of the Royal Society of London Series B, 266, 93–101.CrossRefGoogle Scholar

Bligny, R. and Douce, R. (2001). NMR and plant metabolism. Current Opinion in Plant Biology, 4, 191–196.CrossRefGoogle ScholarPubMed

Bliss, L.C. (1962). Adaptations of arctic and alpine plants to environmental conditions. Arctic, 15, 117–144.CrossRefGoogle Scholar

Blödner, C., Majcherczyk, A., Kües, U., et al. (2007). Early drought induced changes to the needle proteome of Norway spruce. Tree Physiology, 27, 1423–1431.CrossRefGoogle ScholarPubMed

Blom, C.W.P.M. and Voesenek, L.A.C.J. (1996). Flooding: the survival strategies of plants. Trends in Ecology and Evolution, 11, 290–295.CrossRefGoogle Scholar

Bloom, A.J., Smart, D.R., Nguyen, D.T., et al. (2002). Nitrogen assimilation and growth of wheat under elevated carbon dioxide. Proceedings of the National Academy of Sciences of the United States of America, 99, 1730–1735.CrossRefGoogle ScholarPubMed

Blum, A. (2005). Drought resistance, water-use efficiency, and yield potential: are they compatible, dissonant, or mutually exclusive?Australian Journal of Agricultural Research, 56, 1159–1168.CrossRefGoogle Scholar

Blum, A. (2009). Effective use of water (EUW) and not water-use efficiency (WUE) is the target of crop yield improvement under drought stress. Field Crops Research, 112, 119–123.CrossRefGoogle Scholar

Boardman, N.K. (1977). Comparative photosynthesis of sun and shade plants. Annual Review of Plant Physiology, 28, 355–377.CrossRefGoogle Scholar

Boccalandro, H.E., Rugnone, M.L., Moreno, J.E., et al. (2009). Phytochrome B enhances photosynthesis at the expense of water-use efficiency in Arabidopsis. Plant Physiology, 150, 1083–1092.CrossRefGoogle ScholarPubMed

Boccara, M., Boue, C., Garmier, M., et al. (2001). Infrared thermography revealed a role for mitochondria in pre-symptomatic cooling during harpin-induced hypersensitive response. Plant Journal, 28, 663–670.CrossRefGoogle ScholarPubMed

Bode, S., Quentmeier, C.C., Liao, P.-N., et al. (2009). On the regulation of photosynthesis by excitonic interactions between carotenoids and chlorophylls. Proceedings of the National Academy of Sciences USA, 106, 12311–12316.CrossRefGoogle ScholarPubMed

Bogeat-Triboulot, M.B, Brosché, M., Renaut, J., et al. (2007). Gradual soil water depletion results in reversible changes of gene expression, protein profiles, ecophysiology, and growth performance in Populus euphratica, a poplar growing in arid regions. Plant Physiology, 143, 876–892.CrossRefGoogle ScholarPubMed