Stomatal anatomy and closing ability is affected by supplementary light intensity in rose (Rosa hybrida L.)
Blom-Zandstra Margaretha, Pot C.Sander, Maas Frank M., Schapendonk Ad H.C.M. (1995): Effects of different light treatments on the nocturnal transpiration and dynamics of stomatal closure of two Rose cultivars. Scientia Horticulturae, 61, 251-262
https://doi.org/10.1016/0304-4238(94)00751-Z
Boyer J. S., Wong S. C., Farquhar G. D. (1997): CO2 and Water Vapor Exchange across Leaf Cuticle (Epidermis) at Various Water Potentials. Plant Physiology, 114, 185-191
https://doi.org/10.1104/pp.114.1.185
Carvalho Dália R.A., Fanourakis Dimitrios, Correia Maria J., Monteiro José A., Araújo-Alves José Pedro L., Vasconcelos Marta W., Almeida Domingos P.F., Heuvelink Ep, Carvalho Susana M.P. (2016): Root-to-shoot ABA signaling does not contribute to genotypic variation in stomatal functioning induced by high relative air humidity. Environmental and Experimental Botany, 123, 13-21
https://doi.org/10.1016/j.envexpbot.2015.11.001
Domínguez Eva, Heredia-Guerrero José Alejandro, Heredia Antonio (2011): The biophysical design of plant cuticles: an overview. New Phytologist, 189, 938-949
https://doi.org/10.1111/j.1469-8137.2010.03553.x
Drake Paul L., Froend Ray H., Franks Peter J. (2013): Smaller, faster stomata: scaling of stomatal size, rate of response, and stomatal conductance. Journal of Experimental Botany, 64, 495-505
https://doi.org/10.1093/jxb/ers347
Fanourakis Dimitrios, Bouranis Dimitrios, Giday Habtamu, Carvalho Dália R.A., Rezaei Nejad Abdolhossein, Ottosen Carl-Otto (2016): Improving stomatal functioning at elevated growth air humidity: A review. Journal of Plant Physiology, 207, 51-60
https://doi.org/10.1016/j.jplph.2016.10.003
Fanourakis Dimitrios, Carvalho Susana M.P., Almeida Domingos P.F., van Kooten Olaf, van Doorn Wouter G., Heuvelink Ep (2012): Postharvest water relations in cut rose cultivars with contrasting sensitivity to high relative air humidity during growth. Postharvest Biology and Technology, 64, 64-73
https://doi.org/10.1016/j.postharvbio.2011.09.016
Fanourakis Dimitrios, Heuvelink Ep, Carvalho Susana M.P. (2013): A comprehensive analysis of the physiological and anatomical components involved in higher water loss rates after leaf development at high humidity. Journal of Plant Physiology, 170, 890-898
https://doi.org/10.1016/j.jplph.2013.01.013
Fanourakis Dimitrios, Giday Habtamu, Milla Rubén, Pieruschka Roland, Kjaer Katrine H., Bolger Marie, Vasilevski Aleksandar, Nunes-Nesi Adriano, Fiorani Fabio, Ottosen Carl-Otto (2015): Pore size regulates operating stomatal conductance, while stomatal densities drive the partitioning of conductance between leaf sides. Annals of Botany, 115, 555-565
https://doi.org/10.1093/aob/mcu247
Fanourakis Dimitrios, Heuvelink Ep, Carvalho Susana M. P. (2015): Spatial heterogeneity in stomatal features during leaf elongation: an analysis using Rosa hybrida. Functional Plant Biology, 42, 737-
https://doi.org/10.1071/FP15008
Fanourakis Dimitrios, Pieruschka Roland, Savvides Andreas, Macnish Andrew J., Sarlikioti Vaia, Woltering Ernst J. (2013): Sources of vase life variation in cut roses: A review. Postharvest Biology and Technology, 78, 1-15
https://doi.org/10.1016/j.postharvbio.2012.12.001
Fanourakis D., Velez-Ramirez A.I., In B.-C., Barendse H., van Meeteren U., Woltering E.J. (2015): A SURVEY OF PREHARVEST CONDITIONS AFFECTING THE REGULATION OF WATER LOSS DURING VASE LIFE. Acta Horticulturae, , 195-204
https://doi.org/10.17660/ActaHortic.2015.1064.22
Giday Habtamu, Fanourakis Dimitrios, Kjaer Katrine H., Fomsgaard Inge S., Ottosen Carl-Otto (2013): Foliar abscisic acid content underlies genotypic variation in stomatal responsiveness after growth at high relative air humidity. Annals of Botany, 112, 1857-1867
https://doi.org/10.1093/aob/mct220
Giday Habtamu, Kjaer Katrine H., Fanourakis Dimitrios, Ottosen Carl-Otto (2013): Smaller stomata require less severe leaf drying to close: A case study in Rosa hydrida. Journal of Plant Physiology, 170, 1309-1316
https://doi.org/10.1016/j.jplph.2013.04.007
Heuvelink E., Bakker M.J., Hogendonk L., Janse J., Kaarsemaker R., Maaswinkel R. (2006): HORTICULTURAL LIGHTING IN THE NETHERLANDS: NEW DEVELOPMENTS. Acta Horticulturae, , 25-34
https://doi.org/10.17660/ActaHortic.2006.711.1
James S. A., Bell D. T. (2000): Influence of light availability on leaf structure and growth of two Eucalyptus globulus ssp. globulus provenances. Tree Physiology, 20, 1007-1018
https://doi.org/10.1093/treephys/20.15.1007
Kerstiens Gerhard (1996): Cuticular water permeability and its physiological significance. Journal of Experimental Botany, 47, 1813-1832
https://doi.org/10.1093/jxb/47.12.1813
Poorter Hendrik, Niinemets Ülo, Walter Achim, Fiorani Fabio, Schurr Uli (2010): A method to construct dose–response curves for a wide range of environmental factors and plant traits by means of a meta-analysis of phenotypic data. Journal of Experimental Botany, 61, 2043-2055
https://doi.org/10.1093/jxb/erp358
Terashima Ichiro, Hanba Yuko T., Tazoe Youshi, Vyas Poonam, Yano Satoshi (2006): Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO2 diffusion. Journal of Experimental Botany, 57, 343-354
https://doi.org/10.1093/jxb/erj014
Xue Dawei, Zhang Xiaoqin, Lu Xueli, Chen Guang, Chen Zhong-Hua (2017): Molecular and Evolutionary Mechanisms of Cuticular Wax for Plant Drought Tolerance. Frontiers in Plant Science, 8, -
https://doi.org/10.3389/fpls.2017.00621
YANO S., TERASHIMA I. (2004): Developmental process of sun and shade leaves in Chenopodium album L.. Plant, Cell and Environment, 27, 781-793
https://doi.org/10.1111/j.1365-3040.2004.01182.x
Blom-Zandstra Margaretha, Pot C.Sander, Maas Frank M., Schapendonk Ad H.C.M. (1995): Effects of different light treatments on the nocturnal transpiration and dynamics of stomatal closure of two Rose cultivars. Scientia Horticulturae, 61, 251-262
https://doi.org/10.1016/0304-4238(94)00751-Z
Boyer J. S., Wong S. C., Farquhar G. D. (1997): CO2 and Water Vapor Exchange across Leaf Cuticle (Epidermis) at Various Water Potentials. Plant Physiology, 114, 185-191
https://doi.org/10.1104/pp.114.1.185
Carvalho Dália R.A., Fanourakis Dimitrios, Correia Maria J., Monteiro José A., Araújo-Alves José Pedro L., Vasconcelos Marta W., Almeida Domingos P.F., Heuvelink Ep, Carvalho Susana M.P. (2016): Root-to-shoot ABA signaling does not contribute to genotypic variation in stomatal functioning induced by high relative air humidity. Environmental and Experimental Botany, 123, 13-21
https://doi.org/10.1016/j.envexpbot.2015.11.001
Domínguez Eva, Heredia-Guerrero José Alejandro, Heredia Antonio (2011): The biophysical design of plant cuticles: an overview. New Phytologist, 189, 938-949
https://doi.org/10.1111/j.1469-8137.2010.03553.x
Drake Paul L., Froend Ray H., Franks Peter J. (2013): Smaller, faster stomata: scaling of stomatal size, rate of response, and stomatal conductance. Journal of Experimental Botany, 64, 495-505
https://doi.org/10.1093/jxb/ers347
Fanourakis Dimitrios, Bouranis Dimitrios, Giday Habtamu, Carvalho Dália R.A., Rezaei Nejad Abdolhossein, Ottosen Carl-Otto (2016): Improving stomatal functioning at elevated growth air humidity: A review. Journal of Plant Physiology, 207, 51-60
https://doi.org/10.1016/j.jplph.2016.10.003
Fanourakis Dimitrios, Carvalho Susana M.P., Almeida Domingos P.F., van Kooten Olaf, van Doorn Wouter G., Heuvelink Ep (2012): Postharvest water relations in cut rose cultivars with contrasting sensitivity to high relative air humidity during growth. Postharvest Biology and Technology, 64, 64-73
https://doi.org/10.1016/j.postharvbio.2011.09.016
Fanourakis Dimitrios, Heuvelink Ep, Carvalho Susana M.P. (2013): A comprehensive analysis of the physiological and anatomical components involved in higher water loss rates after leaf development at high humidity. Journal of Plant Physiology, 170, 890-898
https://doi.org/10.1016/j.jplph.2013.01.013
Fanourakis Dimitrios, Giday Habtamu, Milla Rubén, Pieruschka Roland, Kjaer Katrine H., Bolger Marie, Vasilevski Aleksandar, Nunes-Nesi Adriano, Fiorani Fabio, Ottosen Carl-Otto (2015): Pore size regulates operating stomatal conductance, while stomatal densities drive the partitioning of conductance between leaf sides. Annals of Botany, 115, 555-565
https://doi.org/10.1093/aob/mcu247
Fanourakis Dimitrios, Heuvelink Ep, Carvalho Susana M. P. (2015): Spatial heterogeneity in stomatal features during leaf elongation: an analysis using Rosa hybrida. Functional Plant Biology, 42, 737-
https://doi.org/10.1071/FP15008
Fanourakis Dimitrios, Pieruschka Roland, Savvides Andreas, Macnish Andrew J., Sarlikioti Vaia, Woltering Ernst J. (2013): Sources of vase life variation in cut roses: A review. Postharvest Biology and Technology, 78, 1-15
https://doi.org/10.1016/j.postharvbio.2012.12.001
Fanourakis D., Velez-Ramirez A.I., In B.-C., Barendse H., van Meeteren U., Woltering E.J. (2015): A SURVEY OF PREHARVEST CONDITIONS AFFECTING THE REGULATION OF WATER LOSS DURING VASE LIFE. Acta Horticulturae, , 195-204
https://doi.org/10.17660/ActaHortic.2015.1064.22
Giday Habtamu, Fanourakis Dimitrios, Kjaer Katrine H., Fomsgaard Inge S., Ottosen Carl-Otto (2013): Foliar abscisic acid content underlies genotypic variation in stomatal responsiveness after growth at high relative air humidity. Annals of Botany, 112, 1857-1867
https://doi.org/10.1093/aob/mct220
Giday Habtamu, Kjaer Katrine H., Fanourakis Dimitrios, Ottosen Carl-Otto (2013): Smaller stomata require less severe leaf drying to close: A case study in Rosa hydrida. Journal of Plant Physiology, 170, 1309-1316
https://doi.org/10.1016/j.jplph.2013.04.007
Heuvelink E., Bakker M.J., Hogendonk L., Janse J., Kaarsemaker R., Maaswinkel R. (2006): HORTICULTURAL LIGHTING IN THE NETHERLANDS: NEW DEVELOPMENTS. Acta Horticulturae, , 25-34
https://doi.org/10.17660/ActaHortic.2006.711.1
James S. A., Bell D. T. (2000): Influence of light availability on leaf structure and growth of two Eucalyptus globulus ssp. globulus provenances. Tree Physiology, 20, 1007-1018
https://doi.org/10.1093/treephys/20.15.1007
Kerstiens Gerhard (1996): Cuticular water permeability and its physiological significance. Journal of Experimental Botany, 47, 1813-1832
https://doi.org/10.1093/jxb/47.12.1813
Poorter Hendrik, Niinemets Ülo, Walter Achim, Fiorani Fabio, Schurr Uli (2010): A method to construct dose–response curves for a wide range of environmental factors and plant traits by means of a meta-analysis of phenotypic data. Journal of Experimental Botany, 61, 2043-2055
https://doi.org/10.1093/jxb/erp358
Terashima Ichiro, Hanba Yuko T., Tazoe Youshi, Vyas Poonam, Yano Satoshi (2006): Irradiance and phenotype: comparative eco-development of sun and shade leaves in relation to photosynthetic CO2 diffusion. Journal of Experimental Botany, 57, 343-354
https://doi.org/10.1093/jxb/erj014
Xue Dawei, Zhang Xiaoqin, Lu Xueli, Chen Guang, Chen Zhong-Hua (2017): Molecular and Evolutionary Mechanisms of Cuticular Wax for Plant Drought Tolerance. Frontiers in Plant Science, 8, -
https://doi.org/10.3389/fpls.2017.00621
YANO S., TERASHIMA I. (2004): Developmental process of sun and shade leaves in Chenopodium album L.. Plant, Cell and Environment, 27, 781-793
https://doi.org/10.1111/j.1365-3040.2004.01182.x