Changes in leaf stomatal conductance, petiole hydraulics and vessel morphology in grapevine (Vitis vinifera cv. Chasselas) under different light and irrigation regimes
Silvina Dayer A , Jorge Perez Peña A , Katia Gindro B , Laurent Torregrosa C , Francine Voinesco B , Liliana Martínez D , Jorge A. Prieto A and Vivian Zufferey B EA INTA EEA Mendoza, San Martín 3853, Luján de Cuyo (5507), Mendoza, Argentina.
B Agroscope, Institut des sciences en production végétale IPV, Route de Duillier 50, 1260 Nyon, Switzerland.
C Montpellier SupAgro, UMR AGAP – DAAV research group, 2 place Viala, 34060 Montpellier Cedex 01, France.
D Cátedra de Fisiología Vegetal, Facultad de Ciencias Agrarias, UNCuyo, Almirante Brown 500, 5507 Chacras de Coria, Argentina.
E Corresponding author. Email: vivian.zufferey@agroscope.admin.ch
Functional Plant Biology 44(7) 679-693 https://doi.org/10.1071/FP16041
Submitted: 1 February 2016 Accepted: 21 March 2017 Published: 1 May 2017
Abstract
Hydraulic conductance and water transport in plants may be affected by environmental factors, which in turn regulate leaf gas exchange, plant growth and yield. In this study, we assessed the combined effects of radiation and water regimes on leaf stomatal conductance (gs), petiole specific hydraulic conductivity (Kpetiole) and anatomy (vessel number and size); and leaf aquaporin gene expression of field-grown grapevines at the Agroscope Research Station (Leytron, Switzerland). Chasselas vines were subjected to two radiation (sun and shade) levels combined with two water (irrigated and water-stressed) regimes. The sun and shade leaves received ~61.2 and 1.48 mol m–2 day–1 of photosynthetically active radiation, respectively, during a clear-sky day. The irrigated vines were watered weekly from bloom to veraison whereas the water-stressed vines did not receive any irrigation during the season. Water stress reduced gs and Kpetiole relative to irrigated vines throughout the season. The petioles from water-stressed vines showed fewer large-sized vessels than those from irrigated vines. The shaded leaves from the irrigated vines exhibited a higher Kpetiole than the sun leaves at the end of the season, which was partially explained by a higher number of vessels per petiole and possibly by the upregulation of some of the aquaporins measured in the leaf. These results suggest that not only plant water status but also the light environment at the leaf level affected leaf and petiole hydraulics.
Additional keywords: aquaporins, hydraulic conductivity, irradiance, stomatal conductance, water stress physiology, xylem.
References
Allen CD, Macalady AK, Chenchouni H, Bachelet D, McDowell N, Vennetier M, Kitzberger T, Rigling A, Breshears DD, Hogg EH, et al (2010) A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests. Forest Ecology and Management 259, 660–684.| A global overview of drought and heat-induced tree mortality reveals emerging climate change risks for forests.Crossref | GoogleScholarGoogle Scholar |
Baaziz KB, Lopez D, Rabot A, Combes D, Gousset A, Bouzid S (2012) Light-mediated k leaf induction and contribution of both the PIP1s and PIP2s aquaporins in five tree species: walnut (Juglans regia) case study. Tree Physiology 32, 423–434.
| Light-mediated k leaf induction and contribution of both the PIP1s and PIP2s aquaporins in five tree species: walnut (Juglans regia) case study.Crossref | GoogleScholarGoogle Scholar |
Bacelar EA, Moutinho-Pereira JM, Gonçalves BC, Ferreira HF, Correia CM (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.
| Changes in growth, gas exchange, xylem hydraulic properties and water use efficiency of three olive cultivars under contrasting water availability regimes.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXislWgtrg%3D&md5=b059f72a1c81f31d16f6b79b34f4dc3cCAS |
Breda N, Granier A, Barataud F, Moyne C (1995) Soil water dynamics in an oak stand. I. Soil moisture, water potentials and water uptake by roots. Plant and Soil 172, 17–27.
Brodribb TJ, Holbrook NM (2003) Stomatal closure during leaf dehydration, correlation with other leaf physiological traits. Plant Physiology 132, 2166–2173.
| Stomatal closure during leaf dehydration, correlation with other leaf physiological traits.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3sXmsVantbc%3D&md5=4a66a55d6e749dc26c7e26a47dc80a94CAS |
Brodribb TJ, Holbrook NM (2006) Declining hydraulic efficiency as transpiring leaves desiccate: two types of response. Plant, Cell & Environment 29, 2205–2215.
| Declining hydraulic efficiency as transpiring leaves desiccate: two types of response.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVaitA%3D%3D&md5=d7f4d303297681c37879f8f98f3e19aeCAS |
Bucci SJ, Scholz FG, Goldstein G, Meinzer F, Sternberg L (2003) Dynamic changes in hydraulic conductivity in petioles of two savanna tree species: factors and mechanisms contributing to the refilling of embolized vessels. Plant, Cell & Environment 26, 1633–1645.
| Dynamic changes in hydraulic conductivity in petioles of two savanna tree species: factors and mechanisms contributing to the refilling of embolized vessels.Crossref | GoogleScholarGoogle Scholar |
Carbonneau A (1998) Irrigation, vignoble et produits de la vigne. In ‘Traité d’Irrigation, Aspects qualitatifs’. (Ed. JR Tiercelin). pp. 257–298. (Lavoisier: Paris)
Charrier G, Torres-Ruiz JM, Badel E, Burlett R, Choat B, Cochard H, Delmas CEL, Domec JC, Jansen S, King A, Lenoir N, Martin-StPaul N, Gambetta GA, Delzon S (2016) Evidence for hydraulic vulnerability segmentation and lack of xylem refilling under tension. Plant Physiology 172, 1657–1668.
| Evidence for hydraulic vulnerability segmentation and lack of xylem refilling under tension.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2sXhs1Oru7c%3D&md5=508e38be83105d9bdf6d7d1176f808e7CAS |
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=f4b81212821cd0618bff9bf8414c8e4cCAS |
Chaves MM, Santos TP, Souza CR, Ortuno MF, Rodrigues ML, Lopes CM, Maroco JP, Pereira JS (2007) Deficit irrigation in grapevine improves water-use efficiency while controlling vigour and production quality. Annals of Applied Biology 150, 237–252.
| Deficit irrigation in grapevine improves water-use efficiency while controlling vigour and production quality.Crossref | GoogleScholarGoogle Scholar |
Choat B, Ball MC, Luly JG, Holtum JAM (2005) Hydraulic architecture of deciduous and evergreen dry rainforest tree species from north-eastern Australia. Trees 19, 305–311.
| Hydraulic architecture of deciduous and evergreen dry rainforest tree species from north-eastern Australia.Crossref | GoogleScholarGoogle Scholar |
Choat B, Sack L, Holbrook NM (2007) Diversity of hydraulic traits in nine Cordia species growing in tropical forests with contrasting precipitation. New Phytologist 175, 686–698.
| Diversity of hydraulic traits in nine Cordia species growing in tropical forests with contrasting precipitation.Crossref | GoogleScholarGoogle Scholar |
Choat B, Drayton WM, Brodersen C, Mattthews MA, Shackel KA, Wada H, McElrone AJ (2010) Measurement of vulnerability to water stress-induced cavitation in grapevine: a comparison of four techniques applied to a long-vesseled species: comparison of vulnerability curve technique in grapevine. Plant, Cell & Environment 33, 1502–1512.
Chouzouri A, Schultz HR (2005) Hydraulic anatomy, cavitation susceptibility and gas-exchange of several grapevine cultivars of different geographical origin. Acta Horticulturae 325–332.
| Hydraulic anatomy, cavitation susceptibility and gas-exchange of several grapevine cultivars of different geographical origin.Crossref | GoogleScholarGoogle Scholar |
Cochard H, Coll L, Roux XL, Améglio T (2002) Unraveling the effects of plant hydraulics on stomatal closure during water stress in walnut. Plant Physiology 128, 282–290.
| Unraveling the effects of plant hydraulics on stomatal closure during water stress in walnut.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XmvVSqtw%3D%3D&md5=5190143c14eb51495b3ec3eda0a408e4CAS |
Cochard H, Nardini A, Coll L (2004) Hydraulic architecture of leaf blades: where is the main resistance? Plant, Cell & Environment 27, 1257–1267.
| Hydraulic architecture of leaf blades: where is the main resistance?Crossref | GoogleScholarGoogle Scholar |
Cochard H, Venisse JS, Barigah TS, Brunel N, Herbette S, Guilliot A, Tyree MT, Sakr S (2007) Putative role of aquaporins in variable hydraulic conductance of leaves in response to light. Plant Physiology 143, 122–133.
| Putative role of aquaporins in variable hydraulic conductance of leaves in response to light.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXpt1OgtQ%3D%3D&md5=ed36f17eee037d66c6de90a960694cf3CAS |
Comstock JP (2002) Hydraulic and chemical signalling in the control of stomatal conductance and transpiration. Journal of Experimental Botany 53, 195–200.
| Hydraulic and chemical signalling in the control of stomatal conductance and transpiration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38XhtlWkt7s%3D&md5=15c0b5619bc1950f5befd9d5fd012da2CAS |
Coombe BG (1995) Growth stages of the grapevine: adoption of a system for identifying grapevine growth stages. Australian Journal of Grape and Wine Research 1, 104–110.
| Growth stages of the grapevine: adoption of a system for identifying grapevine growth stages.Crossref | GoogleScholarGoogle Scholar |
Flexas J, Bota J, Cifre J, Escalona J, Galmés J, Gulías J, Lefi EK, Martínez-Cañellas SF, Moreno MT, Ribas-Carbó M, Riera D, Sampol B, Medrano H (2004) Understanding down-regulation of photosynthesis under water stress: future prospects and searching for physiological tools for irrigation management. Annals of Applied Biology 144, 273–283.
| Understanding down-regulation of photosynthesis under water stress: future prospects and searching for physiological tools for irrigation management.Crossref | GoogleScholarGoogle Scholar |
Flexas J, Baron M, Bota J, Ducruet J-M, Galle A, Galmes J, Jiménez M, Pou A, Ribas-Carbó M, Sajnani C, Tomàs M, Medrano H (2009) Photosynthesis limitations during water stress acclimation and recovery in the drought-adapted Vitis hybrid Richter-110 (V. berlandieri × V. rupestris). Journal of Experimental Botany 60, 2361–2377.
| Photosynthesis limitations during water stress acclimation and recovery in the drought-adapted Vitis hybrid Richter-110 (V. berlandieri × V. rupestris).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXmtlyiurg%3D&md5=a23452c29eded2d3886f4b55602f769bCAS |
Fulton AR, Bucher R, Olson B, Schwankl L, Gilles C, Bertagna N, Walton J, Shackel K (2001) Rapid equilibration of leaf and stem water potential under field conditions in almonds, walnuts and prunes. HortTechnology 11, 609–615.
Galmés J, Pou A, Alsina MM, Tomás M, Medrano H, Flexas J (2007) Aquaporin expression in response to different water stress intensities and recovery in Richter-110 (Vitis sp.): relationship with ecophysiological status. Planta 226, 671–681.
| Aquaporin expression in response to different water stress intensities and recovery in Richter-110 (Vitis sp.): relationship with ecophysiological status.Crossref | GoogleScholarGoogle Scholar |
Guyot G, Scoffoni C, Sack L (2012) Combined impacts of irradiance and dehydration on leaf hydraulic conductance: insights into vulnerability and stomatal control: leaf hydraulic responses to light × dehydration. Plant, Cell & Environment 35, 857–871.
| Combined impacts of irradiance and dehydration on leaf hydraulic conductance: insights into vulnerability and stomatal control: leaf hydraulic responses to light × dehydration.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XosFSqsL0%3D&md5=3204adad527d4ad44ddc42ee8ba75c55CAS |
Heinen RB, Ye Q, Chaumont F (2009) Role of aquaporins in leaf physiology. Journal of Experimental Botany 60, 2971–2985.
| Role of aquaporins in leaf physiology.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXpsValsb0%3D&md5=153ce64533abbe71ce2a1efc30f8766cCAS |
Hochberg U, Albuquerque C, Rachmilevitch S, Cochard H, David‐Schwartz R, Brodersen CR, McElrone A, Windt CW (2016) Grapevine petioles are more sensitive to drought induced embolism than stems: evidence from in vivo MRI and microcomputed tomography observations of hydraulic vulnerability segmentation. Plant, Cell & Environment
| Grapevine petioles are more sensitive to drought induced embolism than stems: evidence from in vivo MRI and microcomputed tomography observations of hydraulic vulnerability segmentation.Crossref | GoogleScholarGoogle Scholar |
Johnson DM, Woodruff DR, McCulloh KA, Meinzer FC (2009) Leaf hydraulic conductance, measured in situ, declines and recovers daily: leaf hydraulics, water potential and stomatal conductance in four temperate and three tropical tree species. Tree Physiology 29, 879–887.
| Leaf hydraulic conductance, measured in situ, declines and recovers daily: leaf hydraulics, water potential and stomatal conductance in four temperate and three tropical tree species.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1Mvhs12isw%3D%3D&md5=3fd580abd0cf8d708a9418e2e66f6b08CAS |
Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, Kawai K, Galbraith D, Bohnert HJ (2001) Gene expression profiles during the initial phase of salt stress in rice. The Plant Cell 13, 889–905.
| Gene expression profiles during the initial phase of salt stress in rice.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjtFajsrw%3D&md5=9daf051e92c262c879ff32e2b1ab2c92CAS |
Kim YX, Steudle E (2009) Gating of aquaporins by light and reactive oxygen species in leaf parenchyma cells of the midrib of Zea mays. Journal of Experimental Botany 60, 547–556.
| Gating of aquaporins by light and reactive oxygen species in leaf parenchyma cells of the midrib of Zea mays.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXivFSmt7s%3D&md5=e52f7815ceb75c0b2309b1134008107aCAS |
Lian HL, Yu X, Lane D, Sun WN, Tang ZC, Su WA (2006) Upland rice and lowland rice exhibited different PIP expression under water deficit and ABA treatment. Cell Research 16, 651–660.
| Upland rice and lowland rice exhibited different PIP expression under water deficit and ABA treatment.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XmvFalsL0%3D&md5=46dd4cf014752640fdfad9bac39a8385CAS |
Lovisolo C, Schubert A (1998) Effects of water stress on vessel size and xylem hydraulic conductivity in Vitis vinifera L. Journal of Experimental Botany 49, 693–700.
Lovisolo C, Schubert A (2006) Mercury hinders recovery of shoot hydraulic conductivity during grapevine rehydration: evidence from a whole-plant approach. New Phytologist 172, 469–478.
| Mercury hinders recovery of shoot hydraulic conductivity during grapevine rehydration: evidence from a whole-plant approach.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xht1GntbrI&md5=22e1a0380be1cdaff38e84ad0de36d53CAS |
Lovisolo C, Perrone I, Hartung W, Schubert A (2008) An abscisic acid-related reduced transpiration promotes gradual embolism repair when grapevines are rehydrated after drought. New Phytologist 180, 642–651.
| An abscisic acid-related reduced transpiration promotes gradual embolism repair when grapevines are rehydrated after drought.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsVKms7vM&md5=75e1ec93fc9e27e7181255d05201de55CAS |
Lovisolo C, Perrone I, Carra A, Ferrandino A, Flexas J, Medrano H, Schubert A (2010) Drought-induced changes in development and function of grapevine (Vitis spp.) organs and in their hydraulic and non-hydraulic interactions at the whole-plant level: a physiological and molecular update. Functional Plant Biology 37, 98–116.
| Drought-induced changes in development and function of grapevine (Vitis spp.) organs and in their hydraulic and non-hydraulic interactions at the whole-plant level: a physiological and molecular update.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtlyhsrs%3D&md5=3a936cf49a5e380fc1e33804593176ebCAS |
Matzner SL, Rettedal DD, Harmon DA, Beukelman MR (2014) Constraints to hydraulic acclimation under reduced light in two contrasting Phaseolus vulgaris cultivars. Journal of Experimental Botany 65, 4409–4418.
| Constraints to hydraulic acclimation under reduced light in two contrasting Phaseolus vulgaris cultivars.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2MXitVGjsrvP&md5=0f6eef153f74f4b8a067016c032206d2CAS |
Maurel C, Verdoucq L, Luu DT, Santoni V (2008) Plant aquaporins: membrane channels with multiple integrated functions. Annual Review of Plant Biology 59, 595–624.
| Plant aquaporins: membrane channels with multiple integrated functions.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXntFaqtr4%3D&md5=b9e3557cf224aea3fef4475df919b2ecCAS |
Nardini A, Salleo S (2000) Limitation of stomatal conductance by hydraulic traits: sensing or preventing xylem cavitation? Trees 15, 14–24.
| Limitation of stomatal conductance by hydraulic traits: sensing or preventing xylem cavitation?Crossref | GoogleScholarGoogle Scholar |
Nardini A, Tyree MT, Salleo S (2001) Xylem cavitation in the leaf of Prunus laurocerasus and its impact on leaf hydraulics. Plant Physiology 125, 1700–1709.
| Xylem cavitation in the leaf of Prunus laurocerasus and its impact on leaf hydraulics.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD3MXjtFKqt7k%3D&md5=ce31eaf5c5daf611f44bd6fddfc7dc6cCAS |
Pfaffl M (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Research 29, e45
| A new mathematical model for relative quantification in real-time RT-PCR.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD38nis12jtw%3D%3D&md5=619ec73493e6f82f0b17304e270f4d2eCAS |
Postaire O, Tournaire-Roux C, Grondin A, Boursiac Y, Morillon R, Schaffner AR, Maurel C (2010) A PIP1 aquaporin contributes to hydrostatic pressure-induced water transport in both the root and rosette of Arabidopsis. Plant Physiology 152, 1418–1430.
| A PIP1 aquaporin contributes to hydrostatic pressure-induced water transport in both the root and rosette of Arabidopsis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXmsF2lsb0%3D&md5=b01d236028d17d23a89a48e8a87948b4CAS |
Pou A, Medrano H, Tomás H, Martorell S, Ribas-Carbó M, Flexas J (2012) Anisohydric behaviour in grapevines results in better performance under moderate water stress and recovery than isohydric behavior. Plant and Soil 359, 335–349.
| Anisohydric behaviour in grapevines results in better performance under moderate water stress and recovery than isohydric behavior.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhtlGmsrrP&md5=427fb2598c8047d509bac5ab41dd2647CAS |
Pou A, Medrano H, Flexas J, Tyerman SD (2013) A putative role for TIP and PIP aquaporins in dynamics of leaf hydraulic and stomatal conductances in grapevine under water stress and re-watering: Grapevine leaf conductances and aquaporins. Plant, Cell & Environment 36, 828–843.
| A putative role for TIP and PIP aquaporins in dynamics of leaf hydraulic and stomatal conductances in grapevine under water stress and re-watering: Grapevine leaf conductances and aquaporins.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXjs1eks74%3D&md5=d694a2003dba8826cd4abbf8d72759c1CAS |
Prado K, Maurel C (2013) Regulation of leaf hydraulics: from molecular to whole plant levels. Frontiers in Plant Science 4, 255
| Regulation of leaf hydraulics: from molecular to whole plant levels.Crossref | GoogleScholarGoogle Scholar |
Prado K, Boursiac Y, Tournaire-Roux C, Monneuse JM, Postaire O, Da Ines O, Schaffner AR, Hem S, Santoni V, Maurel C (2013) Regulation of Arabidopsis leaf hydraulics involves light-dependent phosphorylation of aquaporins in veins. The Plant Cell 25, 1029–1039.
| Regulation of Arabidopsis leaf hydraulics involves light-dependent phosphorylation of aquaporins in veins.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXnsFSisr4%3D&md5=9b380a53e1818107d28766c5bbf0a24aCAS |
Reynolds ES (1963) The use of lead citrate at high pH as an electron-opaque stain in electron microscopy. The Journal of Cell Biology 17, 208–212.
| The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaF3sXktVClu70%3D&md5=657504e7db12263004f8408ad22d7f89CAS |
Rockwell FE, Holbrook NM, Zwieniecki MA (2011) Hydraulic conductivity of red oak (Quercus rubra L.) leaf tissue does not respond to light: Light effects on red oak leaf hydraulics. Plant, Cell & Environment 34, 565–579.
| Hydraulic conductivity of red oak (Quercus rubra L.) leaf tissue does not respond to light: Light effects on red oak leaf hydraulics.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3M3ls1Okuw%3D%3D&md5=3f75bb462c1e62a8325605d502b662d4CAS |
Rockwell FE, Wheeler JK, Holbrook NM (2014) Cavitation and its discontents: opportunities for resolving current controversies. Plant Physiology 164, 1649–1660.
| Cavitation and its discontents: opportunities for resolving current controversies.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC2cXmsV2jsro%3D&md5=4cb867e0e32036b9e7f9b42ab10aa065CAS |
Roland JC, Vian B (1991) General preparation and staining of thin sections. In ‘Electron microscopy of plant cells. (Eds JL Hall, C Hawes) pp. 1–66. (Academic Press: London)
Sack L, Holbrook NM (2006) Leaf hydraulics. Annual Review of Plant Biology 57, 361–381.
| Leaf hydraulics.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XosVKhtrs%3D&md5=cf530f9dbd0bb63d69a3455b756ddc6cCAS |
Sack L, Melcher PJ, Zwieniecki MA, Holbrook NM (2002) The hydraulic conductance of the angiosperm leaf lamina: a comparison of three measurement methods. Journal of Experimental Botany 53, 2177–2184.
| The hydraulic conductance of the angiosperm leaf lamina: a comparison of three measurement methods.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xpt1KgtLg%3D&md5=baea30cd2af01a0e57090301387cc309CAS |
Sack L, Cowan PD, Jaikumar N, Holbrook NM (2003) The ‘hydrology’ of leaves: co-ordination of structure and function in temperate woody species. Plant, Cell & Environment 26, 1343–1356.
| The ‘hydrology’ of leaves: co-ordination of structure and function in temperate woody species.Crossref | GoogleScholarGoogle Scholar |
Sade N, Gebremedhin A, Moshelion M (2012) Risk-taking plants: anisohydric behavior as a stress-resistance trait. Plant Signaling & Behavior 7, 767–770.
| Risk-taking plants: anisohydric behavior as a stress-resistance trait.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3sXhtFGns7k%3D&md5=949386c4a8f9176537ee983577c717abCAS |
Salleo S, Nardini A, Pitt F, Lo Gullo MA (2000) Xylem cavitation and hydraulic control of stomatal conductance in laurel (Laurus nobilis L.). Plant, Cell & Environment 23, 71–79.
| Xylem cavitation and hydraulic control of stomatal conductance in laurel (Laurus nobilis L.).Crossref | GoogleScholarGoogle Scholar |
Salleo S, Lo Gullo MA, Raimondo F, Nardini A (2001) Vulnerability to cavitation of leaf minor veins: any impact on leaf gas exchange? Plant, Cell & Environment 24, 851–859.
| Vulnerability to cavitation of leaf minor veins: any impact on leaf gas exchange?Crossref | GoogleScholarGoogle Scholar |
Schultz HR (2003) Differences in hydraulic architecture account for near-isohydric and anisohydric behaviour of two field-grown Vitis vinifera L. cultivars during drought. Plant, Cell & Environment 26, 1393–1405.
| Differences in hydraulic architecture account for near-isohydric and anisohydric behaviour of two field-grown Vitis vinifera L. cultivars during drought.Crossref | GoogleScholarGoogle Scholar |
Schultz HR, Matthews MA (1993) Xylem development and hydraulic conductance in sun and shade shoots of grapevine (Vitis vinifera L.): evidence that low light uncouples water transport capacity from leaf area. Planta 190, 393–406.
| Xylem development and hydraulic conductance in sun and shade shoots of grapevine (Vitis vinifera L.): evidence that low light uncouples water transport capacity from leaf area.Crossref | GoogleScholarGoogle Scholar |
Scoffoni C, Pou A, Aasamaa K, Sack L (2008) The rapid light response of leaf hydraulic conductance: new evidence from two experimental methods. Plant, Cell & Environment 31, 1803–1812.
| The rapid light response of leaf hydraulic conductance: new evidence from two experimental methods.Crossref | GoogleScholarGoogle Scholar |
Shatil‐Cohen A, Attia Z, Moshelion M (2011) Bundle‐sheath cell regulation of xylem‐mesophyll water transport via aquaporins under drought stress: a target of xylem‐borne ABA? The Plant Journal 67, 72–80.
| Bundle‐sheath cell regulation of xylem‐mesophyll water transport via aquaporins under drought stress: a target of xylem‐borne ABA?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpsVyrtrg%3D&md5=b4a45a9287bb16b95d40a03182eb05ddCAS |
Sperry JS (2000) Hydraulic constraints on plant gas exchange. Agricultural and Forest Meteorology 104, 13–23.
| Hydraulic constraints on plant gas exchange.Crossref | GoogleScholarGoogle Scholar |
Sperry JS, Pockman WT (1993) Limitation of transpiration by hydraulic conductance and xylem cavitation in Betula occidentalis. Plant, Cell & Environment 16, 279–287.
| Limitation of transpiration by hydraulic conductance and xylem cavitation in Betula occidentalis.Crossref | GoogleScholarGoogle Scholar |
Tardieu F, Simonneau T (1998) Variability among species of stomatal control under fluctuating soil water status and evaporative demand: modelling isohydric and anisohydric behaviours. Journal of Experimental Botany 49, 419–432.
| Variability among species of stomatal control under fluctuating soil water status and evaporative demand: modelling isohydric and anisohydric behaviours.Crossref | GoogleScholarGoogle Scholar |
Tyerman SD, Niemietz CM, Bramley H (2002) Plant aquaporins: multifunctional water and solute channels with expanding roles. Plant, Cell & Environment 25, 173–194.
| Plant aquaporins: multifunctional water and solute channels with expanding roles.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xhslaktbk%3D&md5=c32a3139c1b36b432ec2cdd102a98137CAS |
Tyree MT, Ewers FW (1991) The hydraulic architecture of trees and other woody plants. New Phytologist 119, 345–360.
| The hydraulic architecture of trees and other woody plants.Crossref | GoogleScholarGoogle Scholar |
Tyree MT, Sperry JS (1988) Do woody plants operate near the point of catastrophic xylem dysfunction caused by dynamic water stress? Answer from a model. Plant Physiology 88, 574–580.
| Do woody plants operate near the point of catastrophic xylem dysfunction caused by dynamic water stress? Answer from a model.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BC3cnhvVGjtA%3D%3D&md5=080bf0d4ddedccdce98f7e38d8871f9aCAS |
Tyree MT, Nardini A, Salleo S, Sack L, El Omari B (2005) The dependence of leaf hydraulic conductance on irradiance during HPFM measurements: any role for stomatal response? Journal of Experimental Botany 56, 737–744.
| The dependence of leaf hydraulic conductance on irradiance during HPFM measurements: any role for stomatal response?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtV2ruro%3D&md5=3cbd4a59063e0af107ebfb39f4a54aacCAS |
Vandeleur RK, Mayo G, Shelden MC, Gilliham M, Kaiser BN, Tyerman SD (2009) The role of plasma membrane intrinsic protein aquaporins in water transport through roots: diurnal and drought stress responses reveal different strategies between isohydric and anisohydric cultivars of grapevine. Plant Physiology 149, 445–460.
| The role of plasma membrane intrinsic protein aquaporins in water transport through roots: diurnal and drought stress responses reveal different strategies between isohydric and anisohydric cultivars of grapevine.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXjt1WqtL8%3D&md5=a75200f7017d1d4f8e71c694913e293cCAS |
Voicu MC, Cooke JEK, Zwiazek JJ (2009) Aquaporin gene expression and apoplastic water flow in bur oak (Quercus macrocarpa) leaves in relation to the light response of leaf hydraulic conductance. Journal of Experimental Botany 60, 4063–4075.
| Aquaporin gene expression and apoplastic water flow in bur oak (Quercus macrocarpa) leaves in relation to the light response of leaf hydraulic conductance.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXht1WqtLnJ&md5=89c62cc9f59f9bac5e717ae0009dc7ceCAS |
Wheeler JK, Huggett BA, Tofte AN, Rockwell FE, Holbrook NM (2013) Cutting xylem under tension or supersaturated with gas can generate PLC and the appearance of rapid recovery from embolism. Plant, Cell & Environment 36, 1938–1949.
Zimmermann MH (1983) ‘Xylem structure and the ascent of sap.’ (Springer- Science & Business Media: Berlin)
Zufferey V, Cochard H, Ameglio T, Spring JL, Viret O (2011) Diurnal cycles of embolism formation and repair in petioles of grapevine (Vitis vinifera cv. Chasselas). Journal of Experimental Botany 62, 3885–3894.
| Diurnal cycles of embolism formation and repair in petioles of grapevine (Vitis vinifera cv. Chasselas).Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXptFGjs74%3D&md5=3a0cb5a9ad088a91cb25814355a0d35cCAS |
Zwieniecki MA, Hutyra L, Thompson MV, Holbrook NM (2000) Dynamic changes in petiole specific conductivity in red maple (Acer rubrum L.), tulip tree (Liriodendron tulipifera L.) and northern fox grape (Vitis labrusca L.). Plant, Cell & Environment 23, 407–414.
| Dynamic changes in petiole specific conductivity in red maple (Acer rubrum L.), tulip tree (Liriodendron tulipifera L.) and northern fox grape (Vitis labrusca L.).Crossref | GoogleScholarGoogle Scholar |