Soil water availability influences the temperature response of photosynthesis and respiration in a grass and a woody shrub
Tony Joseph A , David Whitehead B and Matthew H. Turnbull A CA School of Biological Sciences, University of Canterbury, Private Bag 4800, Christchurch 8041, New Zealand.
B Landcare Research, PO Box 69040, Lincoln 7640, New Zealand.
C Corresponding author. Email: matthew.turnbull@canterbury.ac.nz
Functional Plant Biology 41(5) 468-481 https://doi.org/10.1071/FP13237
Submitted: 7 August 2013 Accepted: 28 November 2013 Published: 6 January 2014
Abstract
Seedlings of the shrub kānuka (Kunzea ericoides var. ericoides (A. Rich) J. Thompson) and the pasture grass brown top (Agrostis capillarus L.) were grown in intact soil cores in climate-controlled cabinets to analyse the thermal response of leaf-level carbon exchange at four levels of volumetric soil water content (θ). The objective was to resolve the combined effects of relatively rapid and short-term changes in θ and temperature on the thermal responses of both photosynthesis and respiration in these two contrasting plant types. Results showed that θ had a greater effect on the short-term temperature response of photosynthesis than the temperature response of respiration. The optimum value of θ for net photosynthesis was around 30% for both plants. The photosynthetic capacity of kānuka and the grass declined significantly when θ fell below 20%. The temperature sensitivity of photosynthesis was low at low soil water content and increased at moderate to high soil water content in both plant types. Statistical analysis showed that the temperature sensitivity of photosynthetic parameters was similar for both plant types, but the sensitivity of respiratory parameters differed. Respiratory capacity increased with increasing soil water content in kānuka but declined significantly when θ fell below 15%. There was no significant influence of soil water content on respiratory capacity in the grass. Collectively, our results indicate that θ influenced the temperature sensitivity of photosynthesis and respiration, and altered the balance between foliar respiration and photosynthetic capacity in both plant types.
Additional keywords: Agrostis capillarus, kānuka, Kunzea ericoides, soil water content.
References
Amthor JS (1991) Respiration and crop productivity. Plant Growth Regulation 10, 271–273.| Respiration and crop productivity.Crossref | GoogleScholarGoogle Scholar |
Armstrong AF, Badger MR, Day DA, Barthet MM, Smith PMC, Millar AH, Whelan J, Atkin OK (2008) Dynamic changes in the mitochondrial electron transport chain underpinning cold acclimation of leaf respiration. Plant, Cell & Environment 31, 1156–1169.
| Dynamic changes in the mitochondrial electron transport chain underpinning cold acclimation of leaf respiration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtVSgt7rJ&md5=994b60e7e8670aef0d225f22cfa822cdCAS |
Atkin OK, Macherel D (2009) The crucial role of plant mitochondria in orchestrating drought tolerance. Annals of Botany 103, 581–597.
| The crucial role of plant mitochondria in orchestrating drought tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXktVGnu7k%3D&md5=e8bf1cfdaa2a05f6c87b28d266a677a4CAS | 18552366PubMed |
Atkin OK, Tjoelker MG (2003) Thermal acclimation and the dynamic response of plant respiration to temperature. Trends in Plant Science 8, 343–351.
| Thermal acclimation and the dynamic response of plant respiration to temperature.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXls1CjtLk%3D&md5=dba3e1660bd04a80bc9d831efa600834CAS | 12878019PubMed |
Atkin OK, Holly C, Ball MC (2000) Acclimation of snow gum (Eucalyptus pauciflora) leaf respiration to seasonal and diurnal variations in temperature: the importance of changes in the capacity and temperature sensitivity of respiration. Plant, Cell & Environment 23, 15–26.
| Acclimation of snow gum (Eucalyptus pauciflora) leaf respiration to seasonal and diurnal variations in temperature: the importance of changes in the capacity and temperature sensitivity of respiration.Crossref | GoogleScholarGoogle Scholar |
Atkin OK, Zhang Q, Wiskich JT (2002) Effect of temperature on rates of alternative and cytochrome pathway respiration and their relationship with the redox poise of the quinone pool. Plant Physiology 128, 212–222.
| Effect of temperature on rates of alternative and cytochrome pathway respiration and their relationship with the redox poise of the quinone pool.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XmvVSruw%3D%3D&md5=dec07a04f472f17e6c2ef56c0961774aCAS | 11788767PubMed |
Atkin OK, Bruhn D, Hurry VM, Tjoelker MG (2005a) Evans Review no. 2: the hot and the cold: unravelling the variable response of plant respiration to temperature. Functional Plant Biology 32, 87–105.
| Evans Review no. 2: the hot and the cold: unravelling the variable response of plant respiration to temperature.Crossref | GoogleScholarGoogle Scholar |
Atkin OK, Bruhn D, Tjoelker MG (2005b) Response of plant respiration to changes in temperature: mechanisms and consequences of variations in the Q 10 and acclimation. In ‘Plant respiration: from cell to ecosystem’. (Eds H Lambers, M Ribas-Carbo) pp. 95–136. (Springer: Dordrecht)
Atkin OK, Loveys BR, Atkinson LJ, Pons TL (2006a) Phenotypic plasticity and growth temperature: understanding interspecific variability. Journal of Experimental Botany 57, 267–281.
| Phenotypic plasticity and growth temperature: understanding interspecific variability.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XisFKnsg%3D%3D&md5=d596b9d66f0eb2c2f7b69139a35368abCAS | 16371402PubMed |
Atkin OK, Scheurwater I, Pons TL (2006b) 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.
| High thermal acclimation potential of both photosynthesis and respiration in two lowland Plantago species in contrast to an alpine congeneric.Crossref | GoogleScholarGoogle Scholar |
Baldocchi D (2005) The carbon cycle under stress. Nature 437, 483–484.
| The carbon cycle under stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtVajs73M&md5=cdecbe4a5b50833767b0724c9b7d153fCAS | 16177771PubMed |
Bauerle WL, Bowden JD, Wang GG (2007) The influence of temperature on within-canopy acclimation and variation in leaf photosynthesis: spatial acclimation to microclimate gradients among climatically divergent Acer rubrum L. genotypes. Journal of Experimental Botany 58, 3285–3298.
| The influence of temperature on within-canopy acclimation and variation in leaf photosynthesis: spatial acclimation to microclimate gradients among climatically divergent Acer rubrum L. genotypes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXht1Kmt77F&md5=891566e9faf1036ef55d1134c8060f69CAS | 17804430PubMed |
Berry J, Bjorkman O (1980) Photosynthetic response and adaptation to temperature in higher plants. Annual Review of Plant Physiology 31, 491–543.
| Photosynthetic response and adaptation to temperature in higher plants.Crossref | GoogleScholarGoogle Scholar |
Bota J, Medrano H, Flexas J (2004) Is photosynthesis limited by decreased Rubisco activity and RuBP content under progressive water stress? New Phytologist 162, 671–681.
| Is photosynthesis limited by decreased Rubisco activity and RuBP content under progressive water stress?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXltlyrsro%3D&md5=255f4a1c95870b56f35c584e6aacefd7CAS |
Brown M, Whitehead D, Hunt JE, Clough TJ, Arnold GC, Baisden WT, Sherlock RR (2009) Regulation of soil surface respiration in a grazed pasture in New Zealand. Agricultural and Forest Meteorology 149, 205–213.
| Regulation of soil surface respiration in a grazed pasture in New Zealand.Crossref | GoogleScholarGoogle Scholar |
Bunce J (2000) Acclimation of photosynthesis to temperature in eight cool and warm climate herbaceous C3 species: temperature dependence of parameters of a biochemical photosynthesis model. Photosynthesis Research 63, 59–67.
| Acclimation of photosynthesis to temperature in eight cool and warm climate herbaceous C3 species: temperature dependence of parameters of a biochemical photosynthesis model.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXlsVymtb0%3D&md5=e8c6fbb70c10d3ba666b11a89bc64aebCAS | 16252165PubMed |
Chaves MM (1991) Effects of water deficits on carbon assimilation. Journal of Experimental Botany 42, 1–16.
| Effects of water deficits on carbon assimilation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK3MXhtFyntrw%3D&md5=be5b83a48b4282bc6b0f18767d2b9518CAS |
Chaves MM, Maroco JP, Pereira JS (2003) Understanding plant responses to drought –from genes to the whole plant. Functional Plant Biology 30, 239–264.
| Understanding plant responses to drought –from genes to the whole plant.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXjtVKlt7o%3D&md5=308e85a17dc620123b40725d9fc5bb2eCAS |
Ciais P, Reichstein M, Viovy N, Granier A, Ogée J, Allard V, Aubinet M, Buchmann N, Bernhofer C, Carrara A, et al (2005) Europe-wide reduction in primary productivity caused by the heat and drought in 2003. Nature 437, 529–533.
| Europe-wide reduction in primary productivity caused by the heat and drought in 2003.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtVajs7rL&md5=20f493881df55bce959d0b279629a345CAS | 16177786PubMed |
Collier DE, Cummins WR (1996) The rate of development of water deficits affects Saxifraga cernua leaf respiration. Physiologia Plantarum 96, 291–297.
| The rate of development of water deficits affects Saxifraga cernua leaf respiration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK28XivFekt74%3D&md5=e171e4a33312a149475f8b7348a63668CAS |
Cox PM, Betts RA, Jones CD, Spall SA, Totterdell IJ (2000) Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model. Nature 408, 184–187.
| Acceleration of global warming due to carbon-cycle feedbacks in a coupled climate model.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3cXotFChsLk%3D&md5=7a0c7d7df36caae06f36b269406c0051CAS | 11089968PubMed |
Criddle RS, Hopkin MS, McArthur ED, Hansen LD (1994) Plant distribution and the temperature coefficient of metabolism. Plant, Cell & Environment 17, 233–243.
| Plant distribution and the temperature coefficient of metabolism.Crossref | GoogleScholarGoogle Scholar |
Diaz-Espejo A, Walcroft AS, Fernandez JE, Hafidi B, Palomo MJ, Giron IF (2006) Modeling photosynthesis in olive leaves under drought conditions. Tree Physiology 26, 1445–1456.
| Modeling photosynthesis in olive leaves under drought conditions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtlSnur%2FK&md5=377fcb856c155bf0bdd2673546c738bfCAS | 16877329PubMed |
Dillaway DN, Kruger EL (2010) Thermal acclimation of photosynthesis: a comparison of boreal and temperate tree species along a latitudinal transect. Plant, Cell & Environment 33, 888–899.
| Thermal acclimation of photosynthesis: a comparison of boreal and temperate tree species along a latitudinal transect.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXnvVagsLg%3D&md5=06961ac3a68a8d124e3131b91447cbdcCAS |
Dungan RJ, Whitehead D, Duncan RP (2003) Seasonal and temperature dependence of photosynthesis and respiration for two co-occurring broad-leaved tree species with contrasting leaf phenology. Tree Physiology 23, 561–568.
| Seasonal and temperature dependence of photosynthesis and respiration for two co-occurring broad-leaved tree species with contrasting leaf phenology.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXkvVyhtro%3D&md5=826be5c767f4cf58f049a7d3493662edCAS | 12730048PubMed |
Farquhar GD, Sharkey TD (1982) Stomatal conductance and photosynthesis. Annual Review of Plant Physiology 33, 317–345.
| Stomatal conductance and photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL38XktlKjs7o%3D&md5=3a73a520dccb5d008b17264757da14c1CAS |
Farquhar GD, von Caemmerer S (1982) Modeling of photosynthetic response to environmental conditions. In ‘Physiological plant ecology II. Vol. 12B’. (Eds OL Lange, PS Nobel, CB Osmond, H Ziegler) pp. 549–587. (Springer-Verlag: New York)
Farquhar GD, Caemmerer S, Berry JA (1980) A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species. Planta 149, 78–90.
| A biochemical model of photosynthetic CO2 assimilation in leaves of C3 species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaL3cXksVWrt7w%3D&md5=b0753d90a732e686217d58be94f309baCAS | 24306196PubMed |
Flexas J, Medrano H (2002) Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited. Annals of Botany 89, 183–189.
| Drought-inhibition of photosynthesis in C3 plants: stomatal and non-stomatal limitations revisited.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XkslymsLs%3D&md5=6950e97670ca3009c324cbf1597a8dd8CAS | 12099349PubMed |
Flexas J, Bota J, Loreto F, Cornic G, Sharkey TD (2004) Diffusive and metabolic limitations to photosynthesis under drought and salinity in C3 plants. Plant Biology 6, 269–279.
| Diffusive and metabolic limitations to photosynthesis under drought and salinity in C3 plants.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD2c3ksVOlug%3D%3D&md5=7d142b7ea3e4d55721c556d5c0230445CAS | 15143435PubMed |
Flexas J, Galmes J, Ribas-Carbo M, Medrano H (2005) The effects of water stress on plant respiration. In ‘Plant respiration: from cell to ecosystem. Vol. 18.’ (Eds H Lambers, M Ribas-Carbo) pp. 85–94. (Springer: Dordrecht)
Flexas J, Bota J, Galmés J, Medrano H, Ribas-Carbó M (2006) Keeping a positive carbon balance under adverse conditions: responses of photosynthesis and respiration to water stress. Physiologia Plantarum 127, 343–352.
| Keeping a positive carbon balance under adverse conditions: responses of photosynthesis and respiration to water stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XosVKhu7o%3D&md5=d285770523d464463fb48e72249a065bCAS |
Flexas J, Ribas-Carb ÓM, Diaz-Espejo A, Galm ÉSJ, Medrano H (2008) Mesophyll conductance to CO2: current knowledge and future prospects. Plant, Cell & Environment 31, 602–621.
| Mesophyll conductance to CO2: current knowledge and future prospects.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXlvFehtbc%3D&md5=ad6d862d57cb993d28d80dc13c662f62CAS |
Galmés J, Ribas-Carbó M, Medrano H, Flexas J (2007) Response of leaf respiration to water stress in Mediterranean species with different growth forms. Journal of Arid Environments 68, 206–222.
| Response of leaf respiration to water stress in Mediterranean species with different growth forms.Crossref | GoogleScholarGoogle Scholar |
Ghashghaie J, Duranceau M, Badeck FW, Cornic G, Adeline MT, Deleens E (2001) δ13C of CO2 respired in the dark in relation to δ13C of leaf metabolites: comparison between Nicotiana sylvestris and Helianthus annuus under drought. Plant, Cell & Environment 24, 505–515.
| δ13C of CO2 respired in the dark in relation to δ13C of leaf metabolites: comparison between Nicotiana sylvestris and Helianthus annuus under drought.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXkt1Oit7k%3D&md5=67c434bcc8844b34d5a0be2ecdea0c79CAS |
Gifford RM (2003) Plant respiration in productivity models: conceptualisation, representation and issues for global terrestrial carbon-cycle research. Functional Plant Biology 30, 171–186.
| Plant respiration in productivity models: conceptualisation, representation and issues for global terrestrial carbon-cycle research.Crossref | GoogleScholarGoogle Scholar |
Grassi G, Magnani F (2005) Stomatal, mesophyll conductance and biochemical limitations to photosynthesis as affected by drought and leaf ontogeny in ash and oak trees. Plant, Cell & Environment 28, 834–849.
| Stomatal, mesophyll conductance and biochemical limitations to photosynthesis as affected by drought and leaf ontogeny in ash and oak trees.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXms12gsL0%3D&md5=904c1624fcd05f093ea80e006e0dfbc9CAS |
Griffin KL, Turnbull M, Murthy R (2002) Canopy position affects the temperature response of leaf respiration in Populus deltoides. New Phytologist 154, 609–619.
| Canopy position affects the temperature response of leaf respiration in Populus deltoides.Crossref | GoogleScholarGoogle Scholar |
Gulias J, Flexas J, Abadia A, Madrano H (2002) Photosynthetic responses to water deficit in six Mediterranean sclerophyll species: possible factors explaining the declining distribution of Rhamnus ludovici-salvatoris, an endemic Balearic species. Tree Physiology 22, 687–697.
| Photosynthetic responses to water deficit in six Mediterranean sclerophyll species: possible factors explaining the declining distribution of Rhamnus ludovici-salvatoris, an endemic Balearic species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xlsl2murg%3D&md5=409601991b822bb7f41ccfba3509d7b0CAS | 12091150PubMed |
Gunderson CA, Norby RJ, Wullschleger SD (2000) Acclimation of photosynthesis and respiration to simulated climatic warming in northern and southern populations of Acer saccharum: laboratory and field evidence. Tree Physiology 20, 87–96.
| Acclimation of photosynthesis and respiration to simulated climatic warming in northern and southern populations of Acer saccharum: laboratory and field evidence.Crossref | GoogleScholarGoogle Scholar | 12651476PubMed |
Harte J, Shaw R (1995) Shifting dominance within a montane vegetation community: results of a climate-warming experiment. Science 267, 876–880.
| Shifting dominance within a montane vegetation community: results of a climate-warming experiment.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXjslCms78%3D&md5=d78441ec283befcdd912cc4dcb15e17eCAS | 17813919PubMed |
Hewitt AE (1998) ‘New Zealand soil classification.’ (Manaaki Whenua Press: Lincoln, New Zealand)
Hikosaka K, Murakami A, Hirose T (1999) Balancing carboxylation and regeneration of ribulose-1,5-bisphosphate in leaf photosynthesis: temperature acclimation of an evergreen tree, Quercus myrsinaefolia. Plant, Cell & Environment 22, 841–849.
| Balancing carboxylation and regeneration of ribulose-1,5-bisphosphate in leaf photosynthesis: temperature acclimation of an evergreen tree, Quercus myrsinaefolia.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXlsFGnsro%3D&md5=9ee32a295d7288cb7af6bc5ee56f4c5cCAS |
Hikosaka K, Ishikawa K, Borjigidai A, Muller O, Onoda Y (2006) Temperature acclimation of photosynthesis: mechanisms involved in the changes in temperature dependence of photosynthetic rate. Journal of Experimental Botany 57, 291–302.
| Temperature acclimation of photosynthesis: mechanisms involved in the changes in temperature dependence of photosynthetic rate.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XisFKntw%3D%3D&md5=e0418ec0a7c92c5212db2c0710db6e93CAS | 16364948PubMed |
Hoefnagel MHN, Atkin OK, Wiskich JT (1998) Interdependence between chloroplasts and mitochondria in the light and the dark. Biochimica et Biophysica Acta (BBA) – Bioenergetics 1366, 235–255.
Hozain MI, Salvucci ME, Fokar M, Holaday AS (2010) The differential response of photosynthesis to high temperature for a boreal and temperate Populus species relates to differences in Rubisco activation and Rubisco activase properties. Tree Physiology 30, 32–44.
| The differential response of photosynthesis to high temperature for a boreal and temperate Populus species relates to differences in Rubisco activation and Rubisco activase properties.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXks1Sltb0%3D&md5=f7dd906bb665080eaedc49e0999eeba0CAS | 19864261PubMed |
Jones HG (2007) Monitoring plant and soil water status: established and novel methods revisited and their relevance to studies of drought tolerance. Journal of Experimental Botany 58, 119–130.
| Monitoring plant and soil water status: established and novel methods revisited and their relevance to studies of drought tolerance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtlOltrg%3D&md5=d2d20f37479409d2dc7031a72a120352CAS | 16980592PubMed |
Katja H, Irina B, Hiie I, Olav K, Tiit P, Bahtijor R, Mari T, Ülo N (2012) Temperature responses of dark respiration in relation to leaf sugar concentration. Physiologia Plantarum 144, 320–334.
| Temperature responses of dark respiration in relation to leaf sugar concentration.Crossref | GoogleScholarGoogle Scholar |
Kattge J, Knorr W (2007) Temperature acclimation in a biochemical model of photosynthesis: a reanalysis of data from 36 species. Plant, Cell & Environment 30, 1176–1190.
| Temperature acclimation in a biochemical model of photosynthesis: a reanalysis of data from 36 species.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVeiurrE&md5=695a554beb636c357356145dd03ecf94CAS |
Kim J, van Iersel MW (2011) Slowly developing drought stress increases photosynthetic acclimation of Catharanthus roseus. Physiologia Plantarum 143, 166–177.
| Slowly developing drought stress increases photosynthetic acclimation of Catharanthus roseus.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXht1WjtrbM&md5=1b04131885f44fb2fa2e6f051aa0a643CAS | 21645003PubMed |
Kositsup B, Montpied P, Kasemsap P, Thaler P, Améglio T, Dreyer E (2009) Photosynthetic capacity and temperature responses of photosynthesis of rubber trees (Hevea brasiliensis Müll. Arg.) acclimate to changes in ambient temperatures. Trees – Structure and Function 23, 357–365.
| Photosynthetic capacity and temperature responses of photosynthesis of rubber trees (Hevea brasiliensis Müll. Arg.) acclimate to changes in ambient temperatures.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXivFSms70%3D&md5=2d424c502e20dbf721c5d61d7bd7119fCAS |
Larigauderie A, Korner C (1995) Acclimation of leaf dark respiration to temperature in alpine and lowland plant species. Annals of Botany 76, 245–252.
| Acclimation of leaf dark respiration to temperature in alpine and lowland plant species.Crossref | GoogleScholarGoogle Scholar |
Lawlor DW (2002b) Limitation to photosynthesis in water-stressed leaves: stomata vs. metabolism and the role of ATP. Annals of Botany 89, 871–885.
| Limitation to photosynthesis in water-stressed leaves: stomata vs. metabolism and the role of ATP.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsVeitLk%3D&md5=28161a8edf55aab82fee7d75a8c4dbb3CAS | 12102513PubMed |
Lawlor DW (2009) Musings about the effects of environment on photosynthesis. Annals of Botany 103, 543–549.
| Musings about the effects of environment on photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXktVGnu7o%3D&md5=4d84c01ea43dbcb13e36299c49f9a8ceCAS | 19205084PubMed |
Lawlor DW, Cornic G (2002) Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants. Plant, Cell & Environment 25, 275–294.
| Photosynthetic carbon assimilation and associated metabolism in relation to water deficits in higher plants.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xhslakur0%3D&md5=2976b9458aa5c91694e9e77c07899fb1CAS |
Leuning R (2002) Temperature dependence of two parameters in a photosynthesis model. Plant, Cell & Environment 25, 1205–1210.
| Temperature dependence of two parameters in a photosynthesis model.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XnvVWitLg%3D&md5=6b754b3fee947ba27198e87c9c4c0774CAS |
Lewis JD, Phillips NG, Logan BA, Hricko CR, Tissue DT (2011) Leaf photosynthesis, respiration and stomatal conductance in six Eucalyptus species native to mesic and xeric environments growing in a common garden. Tree Physiology 31, 997–1006.
| Leaf photosynthesis, respiration and stomatal conductance in six Eucalyptus species native to mesic and xeric environments growing in a common garden.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhsVCls7jP&md5=b76727d9c24f091e3371631eefe66eaeCAS | 21937672PubMed |
Limousin JM, Misson L, Lavoir AV, Martin NK, Rambal S (2010) Do photosynthetic limitations of evergreen Quercus ilex leaves change with long-term increased drought severity? Plant, Cell & Environment 33, 863–875.
Lin Y-S, Medlyn BE, Ellsworth DS (2012) Temperature responses of leaf net photosynthesis: the role of component processes. Tree Physiology 32, 219–231.
| Temperature responses of leaf net photosynthesis: the role of component processes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XmslGjsb8%3D&md5=b232a4021fe132760083cc153a629fd3CAS | 22278379PubMed |
Lloyd J, Taylor JA (1994) On the temperature dependence of soil respiration. Functional Ecology 8, 315–323.
| On the temperature dependence of soil respiration.Crossref | GoogleScholarGoogle Scholar |
Loik ME, Harte J (1996) High-temperature tolerance of Artemisia tridentata and Potentilla gracilis under a climate change manipulation. Oecologia 108, 224–231.
Loik ME, Harte J (1997) Changes in water relations for leaves exposed to a climate-warming manipulation in the rocky mountains of Colorado. Environmental and Experimental Botany 37, 115–123.
| Changes in water relations for leaves exposed to a climate-warming manipulation in the rocky mountains of Colorado.Crossref | GoogleScholarGoogle Scholar |
Loik ME, Redar SP, Harte J (2000) Photosynthetic responses to a climate-warming manipulation for contrasting meadow species in the Rocky Mountains, Colorado, USA. Functional Ecology 14, 166–175.
| Photosynthetic responses to a climate-warming manipulation for contrasting meadow species in the Rocky Mountains, Colorado, USA.Crossref | GoogleScholarGoogle Scholar |
Loveys BR, Atkinson LJ, Sherlock DJ, Roberts RL, Fitter AH, Atkin OK (2003) Thermal acclimation of leaf and root respiration: an investigation comparing inherently fast- and slow-growing plant species. Global Change Biology 9, 895–910.
| Thermal acclimation of leaf and root respiration: an investigation comparing inherently fast- and slow-growing plant species.Crossref | GoogleScholarGoogle Scholar |
Maricle BR, Adler PB (2011) Effects of precipitation on photosynthesis and water potential in Andropogon gerardii and Schizachyrium scoparium in a southern mixed grass prairie. Environmental and Experimental Botany 72, 223–231.
| Effects of precipitation on photosynthesis and water potential in Andropogon gerardii and Schizachyrium scoparium in a southern mixed grass prairie.Crossref | GoogleScholarGoogle Scholar |
Medlyn BE, Dreyer E, Ellsworth D, Forstreuter M, Harley PC, Kirschbaum MUF, Le Roux X, Montpied P, Strassemeyer J, Walcroft A, Wang K, Loustau D (2002a) Temperature response of parameters of a biochemically based model of photosynthesis. II. A review of experimental data. Plant, Cell & Environment 25, 1167–1179.
| Temperature response of parameters of a biochemically based model of photosynthesis. II. A review of experimental data.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XnvVWitL0%3D&md5=7d83305e56413b982b18cf159d1e0465CAS |
Medlyn BE, Loustau D, Delzon S (2002b) Temperature response of parameters of a biochemically based model of photosynthesis I. Seasonal changes in mature maritime pine (Pinus pinaster Ait.). Plant, Cell & Environment 25, 1155–1165.
| Temperature response of parameters of a biochemically based model of photosynthesis I. Seasonal changes in mature maritime pine (Pinus pinaster Ait.).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XnvVWitLw%3D&md5=a1984636041405febd68ad1e820f650aCAS |
Misson L, Limousin JM, Rodriguez R, Letts MG (2010) Leaf physiological responses to extreme droughts in Mediterranean Quercus ilex forest. Plant, Cell & Environment 33, 1898–1910.
| Leaf physiological responses to extreme droughts in Mediterranean Quercus ilex forest.Crossref | GoogleScholarGoogle Scholar |
Miyazawa Y, Kikuzawa K (2006) Physiological basis of seasonal trend in leaf photosynthesis of five evergreen broad-leaved species in a temperate deciduous forest. Tree Physiology 26, 249–256.
| Physiological basis of seasonal trend in leaf photosynthesis of five evergreen broad-leaved species in a temperate deciduous forest.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhslWqs7w%3D&md5=7ae83e321785fae1b68ff6cb5b2285b6CAS | 16356922PubMed |
Onoda Y, Hikosaka K, Hirose T (2005) The balance between RuBP carboxylation and RuBP regeneration: a mechanism underlying the interspecific variation in acclimation of photosynthesis to seasonal change in temperature. Functional Plant Biology 32, 903–910.
| The balance between RuBP carboxylation and RuBP regeneration: a mechanism underlying the interspecific variation in acclimation of photosynthesis to seasonal change in temperature.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtVKns7%2FN&md5=31c3c76cd4517370f8c93eefa3067cffCAS |
Ow LF, Griffin KL, Whitehead D, Walcroft AS, Turnbull MH (2008a) Thermal acclimation of leaf respiration but not photosynthesis in Populus deltoides × nigra. New Phytologist 178, 123–134.
| Thermal acclimation of leaf respiration but not photosynthesis in Populus deltoides × nigra.Crossref | GoogleScholarGoogle Scholar | 18221247PubMed |
Ow LF, Whitehead D, Walcroft AS, Turnbull MH (2008b) Thermal acclimation of respiration but not photosynthesis in Pinus radiata. Functional Plant Biology 35, 448–461.
| Thermal acclimation of respiration but not photosynthesis in Pinus radiata.Crossref | GoogleScholarGoogle Scholar |
Ow LF, Whitehead D, Walcroft AS, Turnbull MH (2010) Seasonal variation in foliar carbon exchange in Pinus radiata and Populus deltoides: respiration acclimates fully to changes in temperature but photosynthesis does not. Global Change Biology 16, 288–302.
| Seasonal variation in foliar carbon exchange in Pinus radiata and Populus deltoides: respiration acclimates fully to changes in temperature but photosynthesis does not.Crossref | GoogleScholarGoogle Scholar |
Parry MAJ, Andralojc PJ, Khan S, Lea PJ, Keys AJ (2002) Rubisco activity: effects of drought stress. Annals of Botany 89, 833–839.
| Rubisco activity: effects of drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XlsVeitLo%3D&md5=df12d0dfbda72c6ad92236eb122f4d53CAS |
Picon C, Ferhi A, Guehl J-M (1997) Concentration and σ13C of leaf carbohydrates in relation to gas exchange in Quercus robur under elevated CO2 and drought. Journal of Experimental Botany 48, 1547–1556.
Pinheiro JC, Bates DM (Eds) (2000) ‘Mixed-effects models in S and S-Plus.’ (Springer-Verlag: New York)
Reich PB (2010) The carbon dioxide exchange. Science 329, 774–775.
| The carbon dioxide exchange.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtVyktrnO&md5=9a7e2fcb40e539947dda9210f62540daCAS | 20705842PubMed |
Ribas-Carbo M, Taylor NL, Giles L, Busquets S, Finnegan PM, Day DA, Lambers H, Medrano H, Berry JA, Flexas J (2005) Effects of water stress on respiration in soybean (Glycine max. L.) leaves. Plant Physiology 139, 466–473.
| Effects of water stress on respiration in soybean (Glycine max. L.) leaves.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtVCgurrI&md5=6441f074ccbdf0750eb330070e423ac2CAS | 16126857PubMed |
Rodríguez-Calcerrada J, Limousin J-M, Martin-StPaul NK, Jaeger C, Rambal S (2012) Gas exchange and leaf aging in an evergreen oak: causes and consequences for leaf carbon balance and canopy respiration. Tree Physiology 32, 464–477.
| Gas exchange and leaf aging in an evergreen oak: causes and consequences for leaf carbon balance and canopy respiration.Crossref | GoogleScholarGoogle Scholar | 22491489PubMed |
Sage RF, Kubien DS (2007) The temperature response of C3 and C4 photosynthesis. Plant, Cell & Environment 30, 1086–1106.
| The temperature response of C3 and C4 photosynthesis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVeiurrP&md5=594c3d91da854d0188a652fb28f862aeCAS |
Sage RF, Way DA, Kubien DS (2008) Rubisco, Rubisco activase, and global climate change. Journal of Experimental Botany 59, 1581–1595.
| Rubisco, Rubisco activase, and global climate change.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXmtleltLc%3D&md5=0def0f11c423630115da3bdab7ee2730CAS | 18436544PubMed |
Sanhueza C, Bascunan-Godoy L, Corcuera LJ, Turnbull MH (2013) The response of leaf respiration to water stress in Nothofagus species. New Zealand Journal of Botany 51, 88–103.
| The response of leaf respiration to water stress in Nothofagus species.Crossref | GoogleScholarGoogle Scholar |
Santakumari M, Berkowitz GA (1990) Correlation between the maintenance of photosynthesis and in situ protoplast volume at low water potentials in droughted wheat. Plant Physiology 92, 733–739.
| Correlation between the maintenance of photosynthesis and in situ protoplast volume at low water potentials in droughted wheat.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cnhvFCqsA%3D%3D&md5=a947aa4e91b335bf24542bff7a0f93c0CAS | 16667342PubMed |
Schimel DS, House JI, Hibbard KA, Bousquet P, Ciais P, Peylin P, Braswell BH, Apps MJ, Baker D, Bondeau A (2001) Recent patterns and mechanisms of carbon exchange by terrestrial ecosystems. Nature 414, 169–172.
| Recent patterns and mechanisms of carbon exchange by terrestrial ecosystems.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXosFaisLo%3D&md5=c555962c7df3923e2b66167f3983f0f0CAS | 11700548PubMed |
Schulze ED (1986) Carbon dioxide and water vapor exchange in response to drought in the atmosphere and in the soil. Annual Review of Plant Physiology 37, 247–274.
| Carbon dioxide and water vapor exchange in response to drought in the atmosphere and in the soil.Crossref | GoogleScholarGoogle Scholar |
Sergeant K, Spiess N, Renaut J, Wilhelm E, Hausman JF (2011) One dry summer: a leaf proteome study on the response of oak to drought exposure. Journal of Proteomics 74, 1385–1395.
| One dry summer: a leaf proteome study on the response of oak to drought exposure.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpvFGitbk%3D&md5=ab3493ca7cda35b06f50208a70dbfb63CAS | 21439417PubMed |
Silim S, Ryan N, Kubien D (2010) Temperature responses of photosynthesis and respiration in Populus balsamifera L.: acclimation versus adaptation. Photosynthesis Research 104, 19–30.
| Temperature responses of photosynthesis and respiration in Populus balsamifera L.: acclimation versus adaptation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXlsFKltL4%3D&md5=def3f19c7054d873029ce0235ce63a18CAS | 20112068PubMed |
Šircelj H, Tausz M, Grill D, Batič F (2005) Biochemical responses in leaves of two apple tree cultivars subjected to progressing drought. Journal of Plant Physiology 162, 1308–1318.
| Biochemical responses in leaves of two apple tree cultivars subjected to progressing drought.Crossref | GoogleScholarGoogle Scholar | 16425449PubMed |
Slot M, Zaragoza-Castells J, Atkin OK (2008) Transient shade and drought have divergent impacts on the temperature sensitivity of dark respiration in leaves of Geum urbanum. Functional Plant Biology 35, 1135–1146.
| Transient shade and drought have divergent impacts on the temperature sensitivity of dark respiration in leaves of Geum urbanum.Crossref | GoogleScholarGoogle Scholar |
Smith NG, Dukes JS (2013) Plant respiration and photosynthesis in global-scale models: incorporating acclimation to temperature and CO2. Global Change Biology 19, 45–63.
| Plant respiration and photosynthesis in global-scale models: incorporating acclimation to temperature and CO2.Crossref | GoogleScholarGoogle Scholar | 23504720PubMed |
Tenhunen JD, Serra AS, Harley PC, Dougherty RL, Reynolds JF (1990) Factors influencing carbon fixation and water use by mediterranean sclerophyll shrubs during summer drought. Oecologia 82, 381–393.
| Factors influencing carbon fixation and water use by mediterranean sclerophyll shrubs during summer drought.Crossref | GoogleScholarGoogle Scholar |
Tezara W, Mitchell VJ, Driscoll SD, Lawlor DW (1999) Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP. Nature 401, 914–917.
| Water stress inhibits plant photosynthesis by decreasing coupling factor and ATP.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1MXntFyltbo%3D&md5=9b3184e567e8413c34684bc81de6b09fCAS |
Tissue DT, Wright SJ (1995) Effect of seasonal water availability on phenology and the annual shoot carbohydrate cycle of tropical forest shrubs. Functional Ecology 9, 518–527.
| Effect of seasonal water availability on phenology and the annual shoot carbohydrate cycle of tropical forest shrubs.Crossref | GoogleScholarGoogle Scholar |
Tjoelker MG, Oleksyn J, Reich PB (2001) Modelling respiration of vegetation: evidence for a general temperature-dependent Q 10. Global Change Biology 7, 223–230.
| Modelling respiration of vegetation: evidence for a general temperature-dependent Q 10.Crossref | GoogleScholarGoogle Scholar |
Tjoelker MG, Oleksyn J, Lorenc-Plucinska G, Reich PB (2009) Acclimation of respiratory temperature responses in northern and southern populations of Pinus banksiana. New Phytologist 181, 218–229.
| Acclimation of respiratory temperature responses in northern and southern populations of Pinus banksiana.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXhtlaktL0%3D&md5=b34c0c55ea1089f7369ffa80df6c9a66CAS | 18811616PubMed |
Turnbull MH, Whitehead D, Tissue DT, Schuster WSF, Brown KJ, Griffin KL (2001) Responses of leaf respiration to temperature and leaf characteristics in three deciduous tree species vary with site water availability. Tree Physiology 21, 571–578.
| Responses of leaf respiration to temperature and leaf characteristics in three deciduous tree species vary with site water availability.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD38%2Fht1Gquw%3D%3D&md5=3ad426c33e7531f1105f69f7ea2b2dd7CAS | 11390301PubMed |
Turnbull MH, Whitehead D, Tissue DT, Schuster WSF, Brown KJ, Engel VC, Griffin KL (2002) Photosynthetic characteristics in canopies of Quercus rubra, Quercus prinus and Acer rubrum differ in response to soil water availability. Oecologia 130, 515–524.
| Photosynthetic characteristics in canopies of Quercus rubra, Quercus prinus and Acer rubrum differ in response to soil water availability.Crossref | GoogleScholarGoogle Scholar |
Turnbull MH, Whitehead D, Tissue DT, Schuster WSF, Brown KJ, Griffin KL (2003) Scaling foliar respiration in two contrasting forest canopies. Functional Ecology 17, 101–114.
| Scaling foliar respiration in two contrasting forest canopies.Crossref | GoogleScholarGoogle Scholar |
Turnbull MH, Tissue DT, Griffin KL, Richardson SJ, Peltzer DA, Whitehead D (2005) Respiration characteristics in temperate rainforest tree species differ along a long-term soil-development chronosequence. Oecologia 143, 271–279.
| Respiration characteristics in temperate rainforest tree species differ along a long-term soil-development chronosequence.Crossref | GoogleScholarGoogle Scholar | 15657760PubMed |
Vassileva V, Simova-Stoilova L, Demirevska K, Feller U (2009) Variety-specific response of wheat (Triticum aestivum L.) leaf mitochondria to drought stress. Journal of Plant Research 122, 445–454.
| Variety-specific response of wheat (Triticum aestivum L.) leaf mitochondria to drought stress.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXntlOjurw%3D&md5=b572c3702e005ce4286dece2b365c08aCAS | 19319627PubMed |
Vassileva V, Signarbieux C, Anders I, Feller U (2011) Genotypic variation in drought stress response and subsequent recovery of wheat (Triticum aestivum L.). Journal of Plant Research 124, 147–154.
| Genotypic variation in drought stress response and subsequent recovery of wheat (Triticum aestivum L.).Crossref | GoogleScholarGoogle Scholar | 20502935PubMed |
Walcroft AS, Whitehead D, Silvester WB, Kelliher FM (1997) The response of photosynthetic model parameters to temperature and nitrogen concentration in Pinus radiata D. Don. Plant, Cell & Environment 20, 1338–1348.
| The response of photosynthetic model parameters to temperature and nitrogen concentration in Pinus radiata D. Don.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK1cXkslen&md5=3759f1242686b9ddd1d5abca3e3a20f6CAS |
Warren CR (2008) Does growth temperature affect the temperature responses of photosynthesis and internal conductance to CO2? A test with Eucalyptus regnans. Tree Physiology 28, 11–19.
| Does growth temperature affect the temperature responses of photosynthesis and internal conductance to CO2? A test with Eucalyptus regnans.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXitVGrsbk%3D&md5=96255158542e78030e911c7886ad6f70CAS | 17938109PubMed |
Way DA, Oren R (2010) Differential responses to changes in growth temperature between trees from different functional groups and biomes: a review and synthesis of data. Tree Physiology 30, 669–688.
| Differential responses to changes in growth temperature between trees from different functional groups and biomes: a review and synthesis of data.Crossref | GoogleScholarGoogle Scholar | 20368338PubMed |
Way DA, Sage RF (2008) Thermal acclimation of photosynthesis in black spruce (Picea mariana (Mill.) B.S.P.). Plant, Cell & Environment 31, 1250–1262.
| Thermal acclimation of photosynthesis in black spruce (Picea mariana (Mill.) B.S.P.).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXht1SqsbrO&md5=a12ae322b2d3dc03a8da2767044ffca8CAS |
Wei Z, Yanling J, Feng L, Guangsheng Z (2008) Responses of photosynthetic parameters of Quercus mongolica to soil moisture stresses. Acta Ecologica Sinica 28, 2504–2510.
| Responses of photosynthetic parameters of Quercus mongolica to soil moisture stresses.Crossref | GoogleScholarGoogle Scholar |
Wertin TM, McGuire MA, Teskey RO (2011) Higher growth temperatures decreased net carbon assimilation and biomass accumulation of northern red oak seedlings near the southern limit of the species range. Tree Physiology 31, 1277–1288.
| Higher growth temperatures decreased net carbon assimilation and biomass accumulation of northern red oak seedlings near the southern limit of the species range.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xit1yktrk%3D&md5=a5d9e3410e1767d5983a926223287645CAS | 21937670PubMed |
Weston DJ, Bauerle WL, Swire-Clark GA, Moore B, Baird WV (2007) Characterization of Rubisco activase from thermally contrasting genotypes of Acer rubrum (Aceraceae). American Journal of Botany 94, 926–934.
| Characterization of Rubisco activase from thermally contrasting genotypes of Acer rubrum (Aceraceae).Crossref | GoogleScholarGoogle Scholar | 21636461PubMed |
Whitehead D, Griffin KL, Turnbull MH, Tissue DT, Engel VC, Brown KJ, Schuster WS, Walcroft AS (2004a) Response of total night-time respiration to differences in total daily photosynthesis for leaves in a Quercus rubra L. canopy: implications for modelling canopy CO2 exchange. Global Change Biology 10, 925–938.
| Response of total night-time respiration to differences in total daily photosynthesis for leaves in a Quercus rubra L. canopy: implications for modelling canopy CO2 exchange.Crossref | GoogleScholarGoogle Scholar |
Whitehead D, Walcroft AS, Scott NA, Townsend JA, Trotter CM, Rogers GND (2004b) Characteristics of photosynthesis and stomatal conductance in the shrubland species manuka (Leptospermum scoparium) and kanuka (Kunzea ericoides) for the estimation of annual canopy carbon uptake. Tree Physiology 24, 795–804.
| Characteristics of photosynthesis and stomatal conductance in the shrubland species manuka (Leptospermum scoparium) and kanuka (Kunzea ericoides) for the estimation of annual canopy carbon uptake.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXmtVSjtrk%3D&md5=e0523a1e52d1a3407475df0e0ce26d48CAS | 15123451PubMed |
Wohlfahrt G, Bahn M, Haubner E, Horak I, Michaeler W, Rottmar K, Tappeiner U, Cernusca A (1999) Inter-specific variation of the biochemical limitation to photosynthesis and related leaf traits of 30 species from mountain grassland ecosystems under different land use. Plant, Cell & Environment 22, 1281–1296.
| Inter-specific variation of the biochemical limitation to photosynthesis and related leaf traits of 30 species from mountain grassland ecosystems under different land use.Crossref | GoogleScholarGoogle Scholar |
Wythers KR, Reich PB, Tjoelker MG, Bolstad PB (2005) Foliar respiration acclimation to temperature and temperature variable Q 10 alter ecosystem carbon balance. Global Change Biology 11, 435–449.
| Foliar respiration acclimation to temperature and temperature variable Q 10 alter ecosystem carbon balance.Crossref | GoogleScholarGoogle Scholar |
Xu CY, Griffin KL (2006) Seasonal variation in the temperature response of leaf respiration in Quercus rubra: foliage respiration and leaf properties. Functional Ecology 20, 778–789.
| Seasonal variation in the temperature response of leaf respiration in Quercus rubra: foliage respiration and leaf properties.Crossref | GoogleScholarGoogle Scholar |
Xu Z, Zhou G (2011) Responses of photosynthetic capacity to soil moisture gradient in perennial rhizome grass and perennial bunchgrass. BMC Plant Biology 11, 21
| Responses of photosynthetic capacity to soil moisture gradient in perennial rhizome grass and perennial bunchgrass.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXhvFant74%3D&md5=d7b668abccdc5471da643e08bc2f3cf9CAS | 21266062PubMed |
Yamori W, Noguchi K, Terashima I (2005) Temperature acclimation of photosynthesis in spinach leaves: analyses of photosynthetic components and temperature dependencies of photosynthetic partial reactions. Plant, Cell & Environment 28, 536–547.
| Temperature acclimation of photosynthesis in spinach leaves: analyses of photosynthetic components and temperature dependencies of photosynthetic partial reactions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXjs1WltLs%3D&md5=07c8baa0c04cecf4c143ce2c4526100bCAS |
Yamori W, Suzuki K, Noguchi K, Nakai M, Terashima I (2006) Effects of Rubisco kinetics and Rubisco activation state on the temperature dependence of the photosynthetic rate in spinach leaves from contrasting growth temperatures. Plant, Cell & Environment 29, 1659–1670.
| Effects of Rubisco kinetics and Rubisco activation state on the temperature dependence of the photosynthetic rate in spinach leaves from contrasting growth temperatures.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XotlSmur4%3D&md5=e4d77777b5082061b998685fc0766dd5CAS |
Zhou X, Liu X, Wallace LL, Luo Y (2007) Photosynthetic and respiratory acclimation to experimental warming for four species in a tallgrass prairie ecosystem. Journal of Integrative Plant Biology 49, 270–281.
| Photosynthetic and respiratory acclimation to experimental warming for four species in a tallgrass prairie ecosystem.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXjs1Gks7s%3D&md5=98a62a5a1b700be10a31dfce9f2e0195CAS |