Mesophyll porosity is modulated by the presence of functional stomata

[1]  A. Fleming,et al.  Reduced stomatal density in bread wheat leads to increased water-use efficiency , 2019, Journal of experimental botany.

[2]  Christopher Hepworth,et al.  Stomatal development: focusing on the grasses. , 2018, Current opinion in plant biology.

[3]  S. Mooney,et al.  Cell density and airspace patterning in the leaf can be manipulated to increase leaf photosynthetic capacity , 2017, The Plant journal : for cell and molecular biology.

[4]  J. Langdale,et al.  SHORTROOT-Mediated Increase in Stomatal Density Has No Impact on Photosynthetic Efficiency1[CC-BY] , 2017, Plant Physiology.

[5]  J. Berry,et al.  Disruption of stomatal lineage signaling or transcriptional regulators has differential effects on mesophyll development, but maintains coordination of gas exchange , 2017, The New phytologist.

[6]  A. Fleming,et al.  Formation of the Stomatal Outer Cuticular Ledge Requires a Guard Cell Wall Proline-Rich Protein1[CC-BY] , 2017, Plant Physiology.

[7]  H. Quesneville,et al.  Reconciling the evolutionary origin of bread wheat (Triticum aestivum). , 2017, The New phytologist.

[8]  P. Franks,et al.  Increasing water-use efficiency directly through genetic manipulation of stomatal density. , 2015, The New phytologist.

[9]  N. Ori,et al.  Leaf development and morphogenesis , 2014, Development.

[10]  D. Bergmann,et al.  Patterning and processes: how stomatal development defines physiological potential. , 2014, Current opinion in plant biology.

[11]  Dominique C Bergmann,et al.  An integrated model of stomatal development and leaf physiology. , 2014, The New phytologist.

[12]  Craig Sturrock,et al.  Increased leaf mesophyll porosity following transient retinoblastoma-related protein silencing is revealed by microcomputed tomography imaging and leads to a system-level physiological response to the altered cell division pattern , 2013, The Plant journal : for cell and molecular biology.

[13]  Kerstin Pingel,et al.  50 Years of Image Analysis , 2012 .

[14]  Kevin W Eliceiri,et al.  NIH Image to ImageJ: 25 years of image analysis , 2012, Nature Methods.

[15]  K. Torii,et al.  Mechanisms of stomatal development. , 2012, Annual review of plant biology.

[16]  P. Franks,et al.  Genetic manipulation of stomatal density influences stomatal size, plant growth and tolerance to restricted water supply across a growth carbon dioxide gradient , 2012, Philosophical Transactions of the Royal Society B: Biological Sciences.

[17]  Sandra J Shefelbine,et al.  BoneJ: Free and extensible bone image analysis in ImageJ. , 2010, Bone.

[18]  Ü. Niinemets,et al.  Leaf Functional Anatomy in Relation to Photosynthesis1 , 2010, Plant Physiology.

[19]  David J. Beerling,et al.  Maximum leaf conductance driven by CO2 effects on stomatal size and density over geologic time , 2009, Proceedings of the National Academy of Sciences.

[20]  J. Gray,et al.  The Signaling Peptide EPF2 Controls Asymmetric Cell Divisions during Stomatal Development , 2009, Current Biology.

[21]  Ilia J Leitch,et al.  Genome size is a strong predictor of cell size and stomatal density in angiosperms. , 2008, The New phytologist.

[22]  R. Joffre,et al.  Leaf morphology, photochemistry and water status changes in resprouting Quercus ilex during drought. , 2005, Functional plant biology : FPB.

[23]  Nigel J. Livingston,et al.  On the need to incorporate sensitivity to CO2 transfer conductance into the Farquhar–von Caemmerer–Berry leaf photosynthesis model , 2004 .

[24]  Dominique C Bergmann,et al.  Integrating signals in stomatal development. , 2004, Current opinion in plant biology.

[25]  F. Woodward,et al.  The role of stomata in sensing and driving environmental change , 2003, Nature.

[26]  A. Fossey,et al.  Stomatal length and frequency as a measure of ploidy level in black wattle, Acacia mearnsii (de Wild) , 2003 .

[27]  N. Sinha,et al.  Xcl1 causes delayed oblique periclinal cell divisions in developing maize leaves, leading to cellular differentiation by lineage instead of position. , 2002, Development.

[28]  I. Terashima,et al.  Slow development of leaf photosynthesis in an evergreen broad‐leaved tree, Castanopsis sieboldii: relationships between leaf anatomical characteristics and photosynthetic rate , 2001 .

[29]  D. W. James,et al.  Altered body morphology is caused by increased stearate levels in a mutant of Arabidopsis , 1994 .

[30]  Jane Masterson,et al.  Stomatal Size in Fossil Plants: Evidence for Polyploidy in Majority of Angiosperms , 1994, Science.

[31]  T. Sharkey,et al.  Estimation of Mesophyll Conductance to CO(2) Flux by Three Different Methods. , 1992, Plant physiology.

[32]  J. Marrison,et al.  Temporal and Spatial Development of the Cells of the Expanding First Leaf of Arabidopsis thaliana (L.) Heynh , 1991 .

[33]  S. Long,et al.  Separating the contribution of the upper and lower mesophyll to photosynthesis in Zea mays L. leaves , 1989, Planta.

[34]  T. Sachs.  Cellular Interactions in the Development of Stomatal Patterns in Vinca major L , 1979 .

[35]  G. Haberlandt.  Beiträge zur Anatomie und Physiologie der Laubmoose , 1886 .

[36]  PLANT METHODS METHODOLOGY Open Access Methodology , 2022 .

[37]  O. Witte,et al.  Stomatal Size in Fossil Plants : Evidence for Polyploidy in Majority of Angiosperms , 2022 .