PHYSIO-BIBLIOGRAPHY J-L

Jackson M. B., Hall K. C. (1987) – Early stomatal closure in waterlogged pea plants is mediated by abscisic acid in the absence of foliar water deficits – Plant Cell Environ. 10: 121–130 – https://doi.org/10.1111/1365-3040.ep11602085https://onlinelibrary.wiley.com/doi/abs/10.1111/1365-3040.ep11602085 – (On our blog : https://plantstomata.wordpress.com/2018/04/05/early-stomatal-closure-in-waterlogged-pea-plants-is-mediated-by-aba-in-the-absence-of-foliar-water-deficits/ )

Jackson M. B., Kowalewska A. K. B. (1983) – Positive and negative messages from roots induce foliar desiccation and stomatal closure in flooded pea plants – J. Exp. Bot. 34: 493-506 – https://doi.org/10.1093/jxb/34.5.493https://academic.oup.com/jxb/article-abstract/34/5/493/453248?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2020/06/10/messages-from-roots-induce-foliar-desiccation-and-stomatal-closure/

Jackson M. B., Saker L. R., Crisp C. M., Else M. A., Janowiak F. (2003) – Ionic and pH signalling from roots to shoots of flooded tomato plants in relation to stomatal closure – Plant and Soil 253(1): 103–113 – https://link.springer.com/article/10.1023%2FA%3A1024588532535?LI=true – (On our blog : https://plantstomata.wordpress.com/2017/10/05/stomatal-closure-and-ionic-and-ph-signalling-from-roots-to-shoots/)

Jacob J., Lawlor D. W. (1991) – Stomatal and mesophyll limitations of photosynthesis in phosphate deficient sunflower, maize and wheat plants – Journal of Experimental Botany 42: 1003-1011 – DOI: 10.1093/jxb/42.8.1003https://www.researchgate.net/publication/31163283_Stomatal_and_Mesophyll_Limitations_of_Photosynthesis_in_Phosphate_Deficient_Sunflower_Maize_and_Wheat_Plants – (On our blog : https://plantstomata.wordpress.com/2020/02/28/stomatal-and-mesophyll-limitations-of-photosynthesis-in-phosphate-deficient-plants/ )

Jacob T., Ritchie S., Assmann S. M., Gilroy S. (1999) – Abscisic acid signal transduction in guard cells is mediated by phospholipase D activity – Proc. Natl. Acad. Sci. USA 96: 12192–12197 – (On our blog : https://plantstomata.wordpress.com/2016/07/01/aba-signal-transduction-in-stomata-is-mediated-by-pld-activity/)

Jacobs C. M. J., van den Hurk B. M. M., de Bruin H. A. R. (1996) – Stomatal behavior and photosynthetic rate of unstressed grapevines in semi-arid conditions – Agric Forest Meteorology 80: 111–134 – https://doi.org/10.1016/0168-1923(95)02295-3https://www.sciencedirect.com/science/article/pii/0168192395022953 – (On our blog : https://plantstomata.wordpress.com/2019/03/16/stomatal-behavior-of-unstressed-grapevines-in-semi-arid-conditions/ )

Jacobsen S.-E.., Liu F., Jensen C. R. (2009) – Does root-sourced ABA play a role for regulation of stomata under drought in quinoa (Chenopodium quinoa Willd.) – Scientia Horticulturae 122(2): 281-287 – DOI: 10.1016/j.scienta.2009.05.019 – http://static-curis.ku.dk/portal/files/15292895/Jacobsen_SE.pdf – On our blog : https://plantstomata.wordpress.com/2017/09/19/abas-role-for-regulation-of-stomata-under-drought-in-quinoa/)

Jafri A., Ahmad R. (1995) – Effect of soil salinity on leaf development, stomatal size and its distribution in cotton (Gossypium hirsutum L.) – Pakistan Journal of Botany 27: 297-303 –

Jahan M. S., Ogawa K., Nakamura Y., Shimoishi Y., Mori I. C., Murata Y. (2008) – Deficient glutathione in guard cells facilitates abscisic acid-induced stomatal closure but does not affect light-induced stomatal opening – Biosci. Biotechnol. Biochem. 72: 2795–2798 – doi: 10.1271/bbb.80407 – https://www.ncbi.nlm.nih.gov/pubmed/18838781 – (On our blog : https://plantstomata.wordpress.com/2018/12/18/the-role-of-glutathione-gsh-in-stomatal-movements/

Jaiwal P. K., Bhamble S. (1983) – Influence of Morphactin on Leaf Morphology and Stomatal Apparatus of Vigna radiata (L.) Wilczek – Giornale Botanico Italiano 117(1-2): 39-46  – https://doi.org/10.1080/11263508309428078 – https://www.researchgate.net/publication/249034444_Influence_of_Morphactin_on_Leaf_Morphology_and_Stomatal_Apparatus_of_Vigna_radiata_L_Wilczek – (On our blog : https://plantstomata.wordpress.com/2016/07/26/the-effect-of-morphactin-on-stomata/)

Jakobson L.Vaahtera L.Tõldsepp K.Nuhkat M.Wang C.Wang Y.-S.Hõrak H.Valk E.Pechter P.Sindarovska Y.Tang J.Xiao C.Xu Y.Talas U. G.Remm M.Kangasjärvi S.Roelfsema M. R. G.Hu H.Kangasjärvi J.Loog M.Schroeder J. I.Kollist H.Brosché M. (2016) – Natural Variation in Arabidopsis Cvi-0 Accession Uncovers Regulation of Guard Cell CO2 Signaling by MPK12 – doi: https://doi.org/10.1101/073015 – https://www.biorxiv.org/content/early/2016/09/01/073015 – (On our blog : https://plantstomata.wordpress.com/2017/11/13/a-new-function-for-plant-mpks-as-protein-kinase-inhibitors-guard-cell-co2-signaling/)

Jalakas P., Huang Y.-C., Yeh Y.-H., Zimmerli L., Merilo E., Kollist H., Brosché M. (2017) – The role of ENHANCED RESPONSES TO ABA1 (ERA1) in Arabidopsis stomatal responses is beyond ABA signaling – Plant Physiol 174(2): 665–671 – https://doi.org/10.1104/pp.17.00220 – http://www.plantphysiol.org/content/174/2/665 – (On our blog : https://plantstomata.wordpress.com/2017/11/11/a-function-for-era1-in-stomatal-opening/)

Jalakas P., Merilo E., Kollist H., Brosche M. (2018) – ABA‐mediated regulation of stomatal density is OST1‐independent – Plant Direct 2(9): e00082 – https://doi.org/10.1002/pld3.82 – https://onlinelibrary.wiley.com/doi/full/10.1002/pld3.82 – (On our blog : https://plantstomata.wordpress.com/2018/12/13/aba%e2%80%90mediated-regulation-of-stomatal-density-is-ost1%e2%80%90independent/

Jalakas P., Merilo E., Kollist H., Brosche M. (2018) – Complexity of ABA signaling for stomatal development and aperture regulation – BioRxiv May 31, 2018 – doi: https://doi.org/10.1101/335810 – https://www.biorxiv.org/content/early/2018/05/31/335810 – (On our blog : https://plantstomata.wordpress.com/2018/10/06/two-signaling-pathways-to-regulate-stomatal-conductance/ )

Jalakas P., Yarmolinsky D., Hannes Kollist H., Brosche M. (2017) – Isolation of Guard-cell Enriched Tissue for RNA Extraction – Bio-Protocol 7(15) – DOI:   https://bio-protocol.org/e2447 – 10.21769/BioProtoc.2447 – (On our blog : https://plantstomata.wordpress.com/2018/01/18/isolation-of-guard-cell-enriched-tissue-for-rna-extraction/ )

James S. A., Bell D. T. (2000) – Leaf orientation, light interception and stomatal conductance of Eucalyptus globulus ssp. globulus leaves – Tree Physiology 20: 815–823 – (On our blog : https://plantstomata.wordpress.com/2021/12/12/97374/ )

Jamieson A. P., Willmer C. M. (1984) – Functional Stomata in a Variegated Leaf Chimera of Pelargonium zonale L. without Guard Cell Chloroplasts – Journal of Experimental Botany 35(156): 1053-1059 – https://www.jstor.org/stable/23691123?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2019/10/09/chloroplasts-are-not-essential-for-the-normal-functioning-of-stomata/ )

Jammes F., Leonhardt N., Tran D., Bousserouel H., Véry A.-A., Renou J.-P.,Vavasseur A., Kwak J. M., Sentenac H., Bouteau F., Leung J. (2014) – Acetylated 1,3-diaminopropane antagonizes abscisic acid-mediated stomatal closing in Arabidopsis – Plant J. 79: 322–333 – doi: 10.1111/tpj.12564 – https://www.ncbi.nlm.nih.gov/pubmed/24891222 – (On our blog : https://plantstomata.wordpress.com/2018/04/08/acetyl-dap-could-refrain-stomates-from-complete-closure-to-sustain-co2-diffusion/

Jammes F., Song C., Shin D., Munemasa S., Takeda K., Gu D., Choa D., Lee S., Giordo R.,  Sritubtim S., Leonhardt N., Ellis B. E., Murata Y., Kwak J. M. (2009) – MAP kinases MPK9 and MPK12 are preferentially expressed in guard cells and positively regulate ROS-mediated ABA signaling – Proc. Natl. Acad. Sci. U.S.A. 106: 20520–20525 – doi: 10.1073/pnas.0907205106 – (On our blog : https://plantstomata.wordpress.com/2016/07/01/mpk9-and-mpk12-function-downstream-of-ros-to-regulate-guard-cell-aba-signaling-positively/)

Jammes F., Yang X., Xiao S., Kwak J. M. (2011) – Two Arabidopsis guard cell-preferential MAPK genes, MPK9 and MPK12, function in biotic stress response – Plant Signal. Behav. 6: 1875–1877 – doi: 10.4161/psb.6.11.17933 – (On our blog : https://plantstomata.wordpress.com/2016/07/01/regulation-of-stomatal-apertures-by-mpk9-and-mpk12-contributes-to-the-first-line-of-defense-against-pathogens/)

Janan P. D. (1974) – The diffusion of carbon dioxide and water vapour through stomata – J. Expt. Bot. 25: 927-936 –

Jane G.T., Green T. G. A. (1985) – Patterns of stomatal conductance in six evergreen tree species from a new zealand cloud forest – Botanical Gazette 146(3): 413-420 – https://eurekamag.com/research/006/075/006075863.php – (On our blog : https://plantstomata.wordpress.com/2022/01/09/patterns-of-stomatal-conductance-2/ )

Jang C.‐J., Nakajima N., Kondo N. (1996) – Disruption of microtubules by abscisic acid in guard cells of Vicia faba L. – Plant Cell Physiology 37: 697–701 – https://doi.org/10.1093/oxfordjournals.pcp.a029001 – https://academic.oup.com/pcp/article-pdf/37/5/697/5147219/37-5-697.pdf – (On our blog : https://plantstomata.wordpress.com/2018/12/18/disruption-of-microtubules-seems-to-be-a-specific-effect-of-aba-in-stomata/

Jangra R., Damen H., Lee J. S. (2019) – MKP1 acts as a key modulator of stomatal development – Journal Plant Signaling & Behavior 14(7): https://doi.org/10.1080/15592324.2019.1604017https://www.tandfonline.com/doi/abs/10.1080/15592324.2019.1604017 – (On our blog : https://plantstomata.wordpress.com/2019/08/25/a-novel-role-of-mkp1-in-plant-development/ )

Jannat R., Uraji M., Morofuji M., Islam M. M., Bloom R. E., Nakamura Y., McClung C. R., Schroeder J. I., Mori I. C., Murata Y. (2011) – Roles of intracellular hydrogen peroxide accumulation in abscisic acid signaling in Arabidopsis guard cells – J. Plant Physiol. 168: 1919–1926 – doi: 10.1016/j.jplph.2011.05.006 – https://pdfs.semanticscholar.org/e6f7/143785beda04e311bf426915b4527414b827.pdf – (On our blog : https://plantstomata.wordpress.com/2018/04/08/aba-inducible-cytosolic-h2o2-elevation-functions-in-aba-induced-stomatal-closure/ )

Jannat R., Uraji M., Morofuji M., Hossain M. A., Islam M. M., Nakamura Y., Mori I. C., Murata Y. (2011) – The roles of CATALASE2 in abscisic acid signaling in Arabidopsis guard cells – Bioscience, Biotechnology and Biochemistry 75(10): 2034-2036 – DOI: 10.1271/bbb.110344https://www.researchgate.net/publication/51699067_The_roles_of_CATALASE2_in_abscisic_acid_signaling_in_Arabidopsis_guard_cells – (On our blog : https://plantstomata.wordpress.com/2019/10/22/the-roles-of-catalase2-in-aba-signaling-in-stomatal-guard-cells/ )

Janowska B., Mansfeld N., Andrzejak R. (2014) – Effect of BA and GA3 on the Morphological Features of Stomata in the Leaf Epidermis of the Zantedeschia albomaculata cv. ‘Albomaculata’ – Not Bot Horti Agrobo 42(1): 104-108 – http://www.notulaebotanicae.ro/index.php/nbha/article/download/9318/7687 – (On our blog : https://plantstomata.wordpress.com/2015/03/26/stomata-in-zantedeschia-monocots/).

Jansen M. A. K., Van Den Noort R. E.. (2000) – Ultraviolet-B radiation induces complex alterations in stomatal behaviour – Physiol Plant 110: 189–194 – https://doi.org/10.1034/j.1399-3054.2000.110207.xhttps://onlinelibrary.wiley.com/doi/abs/10.1034/j.1399-3054.2000.110207.x – (On our blog : https://plantstomata.wordpress.com/2019/06/27/ultraviolet-b-radiation-induces-complex-alterations-in-stomatal-behaviour/ )

Janu V., Raghuvanshi R. K. (2011) – Microscopic studies on epidermal cells and stomatal behavior of some globular cacti (Mammillaria spp.) – Insight Botany 1(1): 1–4 – DOI: 10.5567/BOTANY-IK.2011.1.4 – http://insightknowledge.org/fulltext/?doi=BOTANY-IK.2011.1.4 – (On our blog : https://plantstomata.wordpress.com/2018/04/17/stomatal-behavior-of-some-globular-cacti/ )

Jara-Rojas F., Ortega-Farias S., Valdés-Gomez H., Poblete C., del Pozo A. (2009) – Model Validation for Estimating the Leaf Stomatal Conductance in cv. Cabernet Sauvignon Grapevines – Chilean Journal of Agricultural Research 69(1): 88-96 – Model_Validation_for_Estimating_the_Leaf.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/21/model-validation-for-estimating-the-leaf-stomatal-conductance/ )

Jarman P. D. (1974) – The diffusion of carbon dioxide and water vapour through stomata – Journal of Experimental Botany 25: 927-936 – https://doi.org/10.1093/jxb/25.5.927 – https://academic.oup.com/jxb/article-abstract/25/5/927/431879?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2018/04/08/diffusion-of-co2-and-water-vapour-through-stomata/ )

Jarvis A. J.Davies W. J. (1998) – The coupled response of stomatal conductance to photosynthesis and transpiration – Journal of Experimental Botany 49: 399406 – DOI: 10.1093/jexbot/49.suppl_1.399 – https://www.jstor.org/stable/23695973?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2018/05/19/stomata-respond-to-a-signal-in-proportion-to-the-degree-to-which-the-photosynthetic-capacity-is-realized/ )

Jarvis A. J., Mansfield T. A., Davies W. J. (2002) – Stomatal behavior, photosynthesis and transpiration under rising CO2 – Plant, Cell and Environment 22: 639–648 – https://doi.org/10.1046/j.1365-3040.1999.00407.xhttps://onlinelibrary.wiley.com/doi/full/10.1046/j.1365-3040.1999.00407.x – (On our blog : https://plantstomata.wordpress.com/2019/11/28/stomatal-behavior-under-rising-co2/ )

Jarvis A. J., Young P. C., Taylor C. J., Davies W. J. (1999) – An analysis of the dynamic response of stomatal conductance to a reduction in humidity over leaves of Cedrella oderata – Plant, Cell & Environm. 22: 913–924 – https://doi.org/10.1046/j.1365-3040.1999.00446.xhttps://onlinelibrary.wiley.com/doi/full/10.1046/j.1365-3040.1999.00446.x – (On our blog : https://plantstomata.wordpress.com/2018/12/18/the-dynamic-response-of-stomatal-conductance-to-a-reduction-in-humidity-over-leaves/ )

Jarvis P. G. (1976) – The interpretation of the variations in leaf water potential and stomatal conductance found in canopies in the field – Philosophical Transactions of the Royal Society London, Series B 273: 593610 – DOI: 10.1098/rstb.1976.0035 http://rstb.royalsocietypublishing.org/content/273/927/593 – (On our blog : https://plantstomata.wordpress.com/2018/05/19/variations-in-leaf-water-potential-and-stomatal-conductance-found-in-canopies/ )

Jarvis P. G. (1980) – Stomatal response to water stress in conifers. In: Turner NC, Kramer PJ (eds) Adaptation of plants to water and high temperatures stress – John Wiley and Sons 105- 122 –

Jarvis P. G. (1981) – Stomatal conductance, gaseous exchange and transpiration – In Plants and their Atmospheric Environment (edited bv Grace J. – Ford E. D. and Jarvis P. G. 175-204 – Blackwells, Oxford –

Jarvis P. G., Mansfield T. A. (1980) – Reduced stomatal responses to light, carbon dioxide and abscisic acid in the presence of sodium ions –  Plant, Cell and Environment 3: 279283 – https://doi.org/10.1111/1365-3040.ep11581831 – – https://onlinelibrary.wiley.com/doi/pdf/10.1111/1365-3040.ep11581831 – (On our blog : https://plantstomata.wordpress.com/2018/04/10/control-of-stomatal-movements-by-light-co2-and-aba-at-the-level-of-cation-uptake-or-extrusion/ )

Jarvis P. G., Mansfield T. A. (1981) – Stomatal Physiology – Edn. Cambridge University Press, London 89-130 – https://books.google.be/books?hl=en&lr=&id=Y1GCxYwNapMC&oi=fnd&pg=PA51&ots=rpWM-Jxvz-&sig=e3vWl4BSP5ZMUgdrtRAMtBFuDEU&redir_esc=y#v=onepage&q&f=false – (On our blog : https://plantstomata.wordpress.com/2017/02/15/physiology-of-stomata/)

Jarvis P.G.McNaughton K.G. (1986) – Stomatal control of transpiration: Scaling up from leaf to region – Adv. Ecol. Res. 15149 – https://doi.org/10.1016/S0065-2504(08)60119-1 – – https://www.sciencedirect.com/science/article/pii/S0065250408601191 – (On our blog : https://plantstomata.wordpress.com/2018/04/17/transpiration-depends-on-stomatal-conductance/ )

Jarvis P. G., Morison J. I. L. (1981) – The control of transpiration and photosynthesis by the stomata. In Stomatal Physiology (eds P.G. Jarvis & T.A. Mansfield)  247–279 – Cambridge University Press, New York –

Jarvis P. G., Rose C. W., Begg J. E. (1967) – An experimental and theoretical comparison of viscous and diffuse resistance to gas flow through amphistomatous leaves – Agr. Meteorol. 4: 103-117 –

Jarvis P. G., Slatyer R. O. (1970) – The role of the mesophyll cell wall in leaf transpiration – Planta 90: 303–322 –https://doi.org/10.1007/BF00386383https://link.springer.com/article/10.1007%2FBF00386383#citeas – (On our blog : https://plantstomata.wordpress.com/2022/01/01/doubt-on-the-validity-of-the-long-standing-assumption-that-the-water-vapour-pressure-at-the-evaporation-sites-stomata-is-equal-to-the-saturation-vapour-pressure-under-all-conditions/ )

Jayakody H., Liu S., Whitty M., Petrie P. (2017) – Microscope image based fully automated stomata detection and pore measurement method for grapevines – Plant Methods 13(1): 94 – https://doi.org/10.1186/s13007-017-0244-9https://plantmethods.biomedcentral.com/articles/10.1186/s13007-017-0244-9 – (On our blog : https://plantstomata.wordpress.com/2019/10/08/fully-automated-stomata-detection-and-pore-measurement-method/ )

Jayakody H. S., Petrie P., de Boer H., Whitty M., (2020) – A Generalised Approach for High-throughput Instance Segmentation of Stomata in Microscope Images – Research Square – doi: 10.21203/rs.3.rs-33223/v1https://www.researchsquare.com/article/rs-33223/v1 – (On our blog : https://plantstomata.wordpress.com/2020/07/27/high-throughput-instance-segmentation-of-stomata-in-microscope-images/ )

Jeffree C. E., Johnson R. P. C., Jarvis P. G. (1971) – Epicuticular wax in the stomatal antechamber of sitka spruce and its effect on the diffusion of water vapour and carbon dioxide – Planta 98: 1-10 – doi: 10.1007/BF00387018https://www.ncbi.nlm.nih.gov/pubmed/24493303 – (On our blog : https://plantstomata.wordpress.com/2018/04/10/wax-filled-stomatal-antechambers-are-excellent-antitranspirants-2/ )

Jefferson J. L., Maxwell R. M., Constantine P. G. (2017) – Exploring the Sensitivity of Photosynthesis and Stomatal Resistance Parameters in a Land Surface Model – AMS – https://doi.org/10.1175/JHM-D-16-0053.1https://journals.ametsoc.org/doi/full/10.1175/JHM-D-16-0053.1 – (On our blog : https://plantstomata.wordpress.com/2020/05/04/sensitivity-of-photosynthesis-and-stomatal-resistance-parameters/ )

Jelbert G. (2018) – Stomatal data vs ice core measurements to measure CO2 levels – https://skepticalscience.com/plant-stomata-co2-levels.htm – (On our blog : https://plantstomata.wordpress.com/2018/03/29/stomatal-data-vs-ice-core-measurements-to-measure-co2-levels/

Jenkins B. C. (1944) – The relations of stomatal size and generation to the yielding ability of bulked wheat hybrids – MSc. Thesis University of Alberta, Department of Field Crops – https://www.biodiversitylibrary.org/item/245140#page/5/mode/1up – (On our blog : https://plantstomata.wordpress.com/2022/01/03/the-relation-between-stomatal-size-and-yield-has-no-selection-value/ )

Jeon B. W., Acharya B. R., Assmann S. M. (2019) – The Arabidopsis heterotrimeric G protein β subunit, AGB1, is required for guard cell calcium sensing and calcium‐induced calcium release – Plant Journ. – https://doi.org/10.1111/tpj.14318 –https://onlinelibrary.wiley.com/doi/abs/10.1111/tpj.14318?af=R – (On our blog : https://plantstomata.wordpress.com/2019/03/19/g-protein-signaling-via-agb1-agg1-agg2-is-essential-for-cao%e2%80%90regulation-of-stomatal-apertures/ )

Jeon B. W., Hwang J. U., Hwang Y., Song W. Y., Fu Y., Gu Y., Bao F., Cho D., Kwak J. M., Yang Z., Lee Y. (2008) – The Arabidopsis small G protein ROP2 is activated by light in guard cells and inhibits light-induced stomatal opening – Plant Cell 20(1): 75-87 – doi:  10.1105/tpc.107.054544 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2254924/ – (On our blog : https://plantstomata.wordpress.com/2018/04/17/rop2-is-activated-by-light-in-guard-cells-and-inhibits-light-induced-stomatal-opening/ )

Jeong H., Ryu J.-H., Na S.-i., Cho J. (2020) – Estimation of Stomatal Conductance using Crop Water Stress Index based on the Thermal Image at a Leaf Scale – EGU2020-11926 – https://doi.org/10.5194/egusphere-egu2020-11926EGU General Assembly 2020 https://meetingorganizer.copernicus.org/EGU2020/EGU2020-11926.html?EGUSphere – (On our blog : https://plantstomata.wordpress.com/2020/06/08/estimation-of-stomatal-conductance-using-crop-water-stress-index/ )

Jewaria P. K., Hara T., Tanaka H., Kondo T., Betsuyaku S., Sawa S., Sakagami Y., Aimoto S., Kakimoto T. (2008) – Differential effects of the peptides stomagen, EPF1, and EPF2 on activation of the MAP kinase MPK6 and the SPCH protein level – Plant Cell Physiol. 49(6): 934-943 – doi: 10.1093/pcp/pct076 – https://www.ncbi.nlm.nih.gov/pubmed/23686240 – (On our blog : https://plantstomata.wordpress.com/2018/04/17/effects-of-epf1-and-epf2-on-activation-of-the-map-kinase-mpk6-and-the-spch-protein-level-in-stomata/ )

Jewer P. C., Incoll L. D. (1980) – Promotion of stomatal opening in the grass Anthephora pubescens Nees by a range of natural and synthetic cytokinins. – Planta150: 218–221 – doi: 10.1007/Bf00390829 – https://www.ncbi.nlm.nih.gov/pubmed/24306685 – (On our blog : https://plantstomata.wordpress.com/2018/04/17/natural-and-synthetic-cytokinins-for-stomatal-opening/ )

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Jewer P. C., Neales T. F., Incoll L. D. (1985) – Stomatal responses to carbon dioxide of isolated epidermis from a C 3 plant, the Argenteum mutant of Pisum sativum L., and a crassulacean-acid-metabolism plant Kalanchoë diagremontiana Hamet et Perr – Planta 164(4): 495-500 – https://www.jstor.org/stable/23388454 – (On our blog : https://plantstomata.wordpress.com/2021/10/18/94546/ )

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Jiao X.-C., Song X.-M., Zhang D.-L., Du Q.-J., Li J.-M. (2019) – Coordination between vapor pressure deficit and CO2 on the regulation of photosynthesis and productivity in greenhouse tomato production – Scientific Reports 9, Article number: 8700  – https://www.nature.com/articles/s41598-019-45232-w – (On our blog : https://plantstomata.wordpress.com/2019/08/13/the-interaction-of-vpd-and-co2-on-plant-water-status-stomatal-characteristics-and-gas-exchange-parameters/ )

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Johansson K. S. L., El-Soda M., Pagel E., Meyer R. C., Tõldsepp K., Nilsson A. K., Brosché M., Kollist H., Uddling J., Andersson M. X. (2020) – Genetic controls of short- and long-term stomatal CO2 responses in Arabidopsis thaliana – Annals of Botany 126(1): 179–190 – https://doi.org/10.1093/aob/mcaa065https://academic.oup.com/aob/article/126/1/179/5820690 – (On our blog : https://plantstomata.wordpress.com/2020/06/23/84937/ )

John Innes Centre (2017) – Changing of the guard: Research sheds light on how plants breathe – Science Daily 2017-09 – https://www.sciencedaily.com/releases/2017/09/170921101743.htm – (On our blog : https://plantstomata.wordpress.com/2017/09/22/the-first-full-3d-model-of-a-guard-cell/)

John Innes Centre (2020) – Plant water saving system works like clockwork, it transpires – https://phys.org/news/2020-03-clockwork-transpires.html – (On our blog : https://plantstomata.wordpress.com/2020/03/18/stomata-and-the-circadian-clock/ )

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Johnson C. (2001) – The getting of plant wisdom – ABC Science 2001 http://www.abc.net.au/science/articles/2001/05/10/293607.htm – (On our blog : https://plantstomata.wordpress.com/2015/03/14/stomata-in-different-levels-of-carbon-dioxide-and-light/ )

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Johnson D. M., Domec J.-C., Woodruff D. R., McCulloh K. A., Meinzer F. C. (2013) – Contrasting hydraulic strategies in two  tropical lianas and their host trees – American Journal of Botany 100(2): 374–383 – doi:10.3732/ajb.1200590https://www.academia.edu/32629516/Johnson_et_al_AJB_2013?email_work_card=view-paper – (On our blog : https://plantstomata.wordpress.com/2022/01/15/reduced-stomatal-conductance-prevented-leaf-or-stem-%ef%bf%bcembolism/ )

Johnson D. M., McCulloh K. A., Meinzer F. C., Woodruff D. R., Eissenstat D. M. (2011) – Hydraulic patterns and safety margins, from stem to stomata, in three eastern U.S. tree species – Tree Physiol. 31(6): 659-668 – doi: 10.1093/treephys/tpr050 – Epub 2011 Jun 30 – PMID: 21724585 – https://www.fs.usda.gov/treesearch/pubs/39940 – (On our blog : https://plantstomata.wordpress.com/2017/09/19/stem-and-leaf-vulnerability-to-hydraulic-dysfunction-and-measuring-in-situ-daily-patterns-of-stomatal-conductance-in-the-field/)

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Jones H. G. (1977) – Transpiration in barley lines with differing stomatal frequencies – J Exp Bot 28162168 – https://doi.org/10.1093/jxb/28.1.162 – https://academic.oup.com/jxb/article-abstract/28/1/162/501971?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2018/04/20/the-size-of-stomata-and-differences-in-stomatal-frequency/ )

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Jones H. G. (1985) – Partitioning stomatal and non-stomatal limitations to photosynthesis – Plant, Cell and Environment 8: 95104 – DOI: 10.1111/j.1365-3040.1985.tb01227.x (On our blog : https://plantstomata.wordpress.com/2016/07/04/stomatal-and-non-stomatal-limitations-to-photosynthesis/ )

Jones H. G. (1987) – Breeding for stomatal characters – In: Stomatal Function Eds. E. Zeiger, G.D. Farquhar, I.R. Cowan – Stanford University Press, Stanford., 431-443 –

Jones H.G. (1998) – Stomatal control of photosynthesis and transpiration – J. Exp. Bot. 49: 387-398 – http://jxb.oxfordjournals.org/content/49/Special_Issue/387.short – (On our blog :  https://plantstomata.wordpress.com/2016/02/15/the-control-exerted-by-stomata-over-transpiration-and-photosynthesis/ ).

Jones H. G. (1999) – Use of thermography for quantitative studies of spatial and temporal variation of stomatal conductance over leaf surfaces – Plant Cell Environ 22: 1043–1055 – DOI: 10.1046/j.1365-3040.1999.00468.x – (On our blog : https://plantstomata.wordpress.com/2016/07/04/thermography-and-stomatal-conductance/ )

Jones H. G. (1999) – Use of infrared thermometry for estimation of stomatal conductance in irrigation scheduling – Agricultural and Forest Meteorology 95: 139–149 – https://doi.org/10.1016/S0168-1923(99)00030-1 – https://www.sciencedirect.com/science/article/pii/S0168192399000301 – (On our blog : https://plantstomata.wordpress.com/2019/02/06/infrared-thermometry-for-estimation-of-stomatal-conductance/ )

Jones H. G. (2013) – Stomata – In Plants and Microclimate: A Quantitative Approach to Environmental Plant Physiology (122-152) – Cambridge: Cambridge University Press – doi:10.1017/CBO9780511845727.007https://www.cambridge.org/core/books/abs/plants-and-microclimate/stomata/AFF4FF56E4359AEB99825BEE75EED3FF# – (On our blog : https://plantstomata.wordpress.com/2022/03/15/smartphone-stomata-detection-to-rapidly-characterize-leaf-surface-and-smartphone-based-nanosensor-detection-for-in-field-applications-of-plant-nanobionics/ )

Jones H. G., Fanjul L (1983) – Effects of water stress and CO2 exchange in apple – In: Stress Effects on Photosynthesis (R Marcelle, ed) 75-84 –

Jones H. G.Stoll M.Santos T.de Sousa C.Chaves M. M.Grant O. M. (2002) – Use of infrared thermography for monitoring stomatal closure in the field: application to grapevine – Journal of Experimental Botany 5322492260 – PMID: 12379792  – https://www.ncbi.nlm.nih.gov/pubmed/12379792 – (On our blog : https://plantstomata.wordpress.com/2018/04/11/infrared-thermography-for-monitoring-stomatal-closure/

Jones H. G., Sutherland R.A. (1991) – Stomatal control of xylem embolism – Plant Cell Environ. 14(6): 607-612 – doi:10.1111/j.1365-3040.1991.tb01532.x  – https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-3040.1991.tb01532.x – (On our blog : https://plantstomata.wordpress.com/2018/04/19/stomatal-control-of-xylem-embolism/ )

Jones L., Milne J. L., Ashford D., McCann M. C., McQueen-Mason S. J. (2005) – A conserved functional role of pectic polymers in stomatal guard cells from a range of plant species – Planta 221: 255–264 – DOI: 10.1007/s00425-004-1432-1  – https://www.ncbi.nlm.nih.gov/pubmed/15578215 – (On our blog : https://plantstomata.wordpress.com/2018/04/10/pectins-and-phenolic-esters-have-a-conserved-functional-role-in-stomatal-guard-cell-walls/ ):

Jones L. A. (2011) – Anatomical adaptations of four Crassula species to water availability – Bioscience Horizons 4(1,1): 13–22 – https://doi.org/10.1093/biohorizons/hzr002 – https://academic.oup.com/biohorizons/article/4/1/13/238409 – (On our blog : https://plantstomata.wordpress.com/2018/04/13/stomatal-adaptations-to-water-availability/ )

Jones M. M., Rawson H. M. (2006) – Influence of Rate of Development of Leaf Water Deficits upon Photosynthesis, Leaf Conductance, Water Use Efficiency, and Osmotic Potential in Sorghum – Physiologia Plantarum 45(1): 103-111 – DOI: 10.1111/j.1399-3054.1979.tb01672.xhttps://www.researchgate.net/publication/229898840_Influence_of_Rate_of_Development_of_Leaf_Water_Deficits_upon_Photosynthesis_Leaf_Conductance_Water_Use_Efficiency_and_Osmotic_Potential_in_Sorghum – (On our blog : https://plantstomata.wordpress.com/2021/01/07/stomatal-closure-occurs-slowly-over-a-wide-range-of-leaf-water-potential-the-range-being-greater-for-slower-rates-of-stress/ )

Jones M. R., Leith I. D., Raven J. A., Fowler D., Sutton M. A., Nemitz E., Cape J. N.,  Sheppard L. J., Smith R. I. (2007) – Concentration-dependent NH3 deposition processes for moorland plant species with and without stomata – Atmospheric Environment 41(39): 8980-8994 – DOI: 10.1016/j.atmosenv.2007.08.015 – https://www.infona.pl/resource/bwmeta1.element.elsevier-5c59d159-9a8b-3414-833c-9e9a06771f12 – (On our blog : https://plantstomata.wordpress.com/2017/10/07/concentration-dependent-nh3-deposition-processes-with-and-without-stomata/)

Jones R. J.
, Mansfield T. A. (
1970) Suppression of stomatal opening in leaves treated with abscisic acid. Journal of Experimental Botany 21: 714719 – doi: 10.1093/jxb/21.3.714 – (On our blog : https://plantstomata.wordpress.com/2016/07/04/aba-and-stomatal-behaviour/)

Jones R. J., Mansfield T. A. (1972) – Effects of abscisic acid and its esters on stomatal aperture and the transpiration ratio – Physiol.
Plant. 26: 321-327 – https://doi.org/10.1111/j.1399-3054.1972.tb01117.xhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-3054.1972.tb01117.x – (On our blog : https://plantstomata.wordpress.com/2020/06/10/effects-of-aba-and-its-esters-on-stomatal-aperture/ )

Jorba J., Tapia L., Sant D. (1985) – Photosynthesis, leaf water potential, and stomatal conductance in Olea europaea under wet and drought conditions – Acta Hortic. 171: 237-246 – doi: 10.17660/ActaHortic.1985.171.21 – https://www.actahort.org/books/171/171_21.htm – (On our blog : https://plantstomata.wordpress.com/2019/02/07/stomatal-conductance-in-olive-trees-under-wet-and-drought-conditions/ )

Jordan F. L., Yoklic M., Morino K., Brown P., Seaman R., Glenn E. P., (2009) – Consumptive water use and stomatal conductance of Atriplex lentiformis irrigated with industrial brine in a desert irrigation district – Agricultural and Forest Meteorology 149(5): 899-912 – https://doi.org/10.1016/j.agrformet.2008.11.010 – http://www.sciencedirect.com/science/article/pii/S0168192308003201 – (On our blog : https://plantstomata.wordpress.com/2017/10/02/consumptive-water-use-and-stomatal-conductance/)

Jordan G. J., Carins-Murphy M., Brodribb T. (2014) – Acclimation to humidity modifies the link between leaf size and the density of veins and stomata – (http://www.brodribblab.org.au/publication/acclimation-to-humidity-modifies-the-link-between-leaf-size-and-the-density-of-veins-and-stomata/) – (On our blog : https://plantstomata.wordpress.com/2015/01/30/stomata-during-leaf-acclimation/).

Jordan G. J., Carins-Murphy M., Brodribb T. (2016) – Cell expansion not cell differentiation predominantly co-ordinates veins and stomata within and among herbs and woody angiosperms grown under sun and shade – Ann. Bot. – http://www.brodribblab.org.au/publication/cell-expansion-not-cell-differentiation-predominantly-co-ordinates-veins-and-stomata-within-and-among-herbs-and-woody-angiosperms-grown-under-sun-and-shade/ – (On our blog : https://plantstomata.wordpress.com/2017/09/30/57420/)

Jordan G.J., Carpenter R. J., Brodribb T. J. (2014) – Using fossil leaves as evidence for open vegetation – Palaeogeography, Palaeoclimatology, Palaeoecology 395: 168-175 – DOI: 10.1016/j.palaeo.2013.12.035 – https://www.infona.pl/resource/bwmeta1.element.elsevier-440650e4-46ff-39f0-acb4-c501b3707339 – (On our blog : https://plantstomata.wordpress.com/2017/10/07/amphistomatic-fossil-leaves-of-dicotyledonous-angiosperms-provide-a-strong-proxy-for-open-vegetation/)

Jordan G. J., Carpenter R. J., Holland B. R., Beeton N. J., Woodhams M. D., Brodribb T. J. (2020) – Links between environment and stomatal size through evolutionary time in Proteaceae – Proc. Royal Soc. B – https://doi.org/10.1098/rspb.2019.2876https://royalsocietypublishing.org/doi/full/10.1098/rspb.2019.2876 – (On our blog : https://plantstomata.wordpress.com/2020/01/30/stomatal-size-is-significantly-affected-by-environmental-factors-other-than-atmospheric-co2/ )

Jordan G. J., Carpenter R. J., Koutoulis A., Price A., Brodribb T. J. (2015) – Environmental adaptation in stomatal size independent of the effects of genome size. – New Phytol. 205(2): 608-617 – doi: 10.1111/nph.13076. Epub 2014 Sep 30 – PMID: 25266914 – (On our blog : https://plantstomata.wordpress.com/2016/02/19/6196/).

Jordan G. J. Weston P. H.Carpenter R. J. Dillon R. A., Brodribb T. J. (2008) – The evolutionary relations of sunken, covered, and encrypted stomata to dry habitats in Proteaceae – Amer. J. Bot. 95(5): 521-530 – (http://www.amjbot.org/content/95/5/521.full) – (On our blog : https://plantstomata.wordpress.com/2015/03/29/sunken-covered-and-encrypted-stomata/).

Jordan W. R., Brown K. W., Thomas J. C. (1975) – Leaf age as a determinant in stomatal control of water loss from cotton during water stress. – Plant Physiology 56: 595599 – https://doi.org/10.1104/pp.56.5.595 – http://www.plantphysiol.org/content/56/5/595 – (On our blog : https://plantstomata.wordpress.com/2018/04/19/leaf-age-as-a-determinant-in-stomatal-control-of-water-loss/ )

Jordan-Meille L., Martineau E., Bornot Y., Lavres J., Abreu-Junior C. H., Domec J.-C. (2018) – How Does Water-Stressed Corn Respond toPotassium Nutrition? A Shoot-Root Scale ApproachStudy under Controlled Conditions – Agriculture 8: 180 – doi: 10.3390/agriculture8110180 – https://www.academia.edu/37951082/How_Does_Water-Stressed_Corn_Respond_to_Potassium_Nutrition_A_Shoot-Root_Scale_Approach_Study_under_Controlled_Conditions?email_work_card=title – (On our blog : https://plantstomata.wordpress.com/2018/12/11/water-stress-and-potassium-nutrition/

Joshi P., Joshi N., Purohit S. D. (2006) – Stomatal characteristics during micropropagation of Wrightia tomentosa – Biologia Plantarum 2006: 275-278 – DOI:10.1007/s10535-006-0019-zhttps://www.semanticscholar.org/paper/Stomatal-characteristics-during-micropropagation-of-Joshi-Joshi/cc84812061281afcf6555fc89e0186ca317da0c6 – (On our blog : https://plantstomata.wordpress.com/2020/02/17/stomatal-characteristics-during-micropropagation-2/ )

Joshi-Saha A., Valon C., Leung, J. A. (2011) – Brand New START: abscisic acid perception and transduction in the guard cell – Sci. Signal. 4:re4 – doi: 10.1126/scisignal.2002164 – http://stke.sciencemag.org/content/4/201/re4.full – (On our blog : https://plantstomata.wordpress.com/2018/04/11/aba-perception-and-transduction-in-stomata/ )

Josifoski R. (2018) – Plant Stomata density is related to the plant adaptation in the environment – Griffith University 1041 SCG Biological Systems – Lab Report 2 – Plant_Stomata_density_is_related_to_the.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/22/plant-stomata-density-and-adaptation-in-the-environment/ )

Jossier M., Kroniewicz L., Dalmas F., Le Thiec D., Ephritikhine G., Thomine S., Barbier-Brygoo H., Vavasseur A., Filleur S., Leonhardt N. (2010) – The Arabidopsis vacuolar anion transporter, AtCLCc, is involved in the regulation of stomatal movements and contributes to salt tolerance – Plant J. 64: 563576 – doi: 10.1111/j.1365-313X.2010.04352.x –  (On our blog : https://plantstomata.wordpress.com/2016/07/04/atclcc-stomatal-movements-and-salt-tolerance/)

Jost M., Glatki Jost M. (1975) – The relative water content in flag leaves of wheat (T. aestivum subsp. vulgare) in relation to the number and size of stomata – Agronomski Glasnik 37(5/6): 285-294 – https://eurekamag.com/research/000/552/000552231.php – (On our blog : https://plantstomata.wordpress.com/2022/02/19/the-relative-water-content-in-flag-leaves-of-wheat-in-relation-to-the-number-and-size-of-stomata/ )

Joudoi T., Shichiri Y., Kamizono N., Akaike T., Sawa T., Yoshitake J., Yamada N., Iwai S. (2013) – Nitrated cyclic GMP modulates guard cell signaling in Arabidopsis – Plant Cell 25: 558–571 – doi: 10.1105/tpc.112.105049 – (On our blog : https://plantstomata.wordpress.com/2016/07/04/8-nitro-cgmp-acts-as-a-guard-cell-signaling-molecule-in-stomata/)

Jover-Gil S.Candela H.Robles P.Aguilera V.Barrero J. M.Micol J. L., Ponce M. R. (2012) – The MicroRNA Pathway Genes AGO1, HEN1and HYL1 Participate in Leaf Proximal–Distal, Venation and Stomatal Patterning in Arabidopsis – Plant Cell Physiol 53(7): 1322-1333 – doi: 10.1093/pcp/pcs077  http://pcp.oxfordjournals.org/content/53/7/1322.abstract – (On our blog : https://plantstomata.wordpress.com/2016/03/24/the-microrna-pathway-genes-ago1-hen1and-hyl1-and-stomata/)

Juárez C. (2011) Caracterización química y estomática y\ crecimiento de tallos de Acanthocereus tetragonusA. subinermis e Hylocereus undatus – Tesis, Maestría en Ciencias (Master of Science thesis). Colegio de PostgraduadosEdo. de México. México. pp. 44 –  

Juárez Lopez J. F. (xxxx) Respuesta de la fotosíntesis a la concentración de CO2 : limitaciones estomáticas y bioquímicas de la fotosíntesis en Quercus ilex Subsp Ballota y Q. fagineaTesis Universidad de Salamanca, Facultad de Biología, Area de Ecología –

Juenger T., McKay J. K., Hausmann N., Keurntjes J. J. B., Sen S., Stowe K. A., Dawson T. E., Simms E. L., Richards J. H. (2005) – Identification and characterization of QTL underlying whole‐plant physiology in Arabidopsis thaliana: δ13C, stomatal conductance and transpiration efficiency – Plant, Cell & Environment 28(6): 697-708 –https://doi.org/10.1111/j.1365-3040.2004.01313.xhttps://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-3040.2004.01313.x – (On our blog : https://plantstomata.wordpress.com/2019/11/02/allelic-effects-on-%ce%b413c-through-the-upstream-trait-of-stomatal-conductance-with-subsequent-consequences-for-whole-plant-transpiration-efficiency-and-water-loss/ )

Juma M. A., Hornung R. K. W. (1998) – Effects of induced water stress on coconut leaf stomata –

Jumrani K., Bhatia V. S., Pandey G. P. (2017) – Impact of elevated temperatures on specific leaf weight, stomatal density, photosynthesis and chlorophyll fluorescence in soybean – Photosynthesis Research 131: 333–350 – https://doi.org/10.1007/s11120-016-0326-yhttps://link.springer.com/article/10.1007/s11120-016-0326-y#citeas – (On our blog : https://plantstomata.wordpress.com/2019/06/13/elevated-temperatures-and-stomatal-density/ )

Jung C., Seo J. S., Han S. W., Koo Y. J., Kim C. H., Song S. I., Nahm B. H., Choi Y. D., Cheong J.-J. (2007) – Overexpression of AtMYB44 enhances stomatal closure to confer abiotic stress tolerance in transgenic Arabidopsis – Plant Physiol. 146: 623–635 – https://doi.org/10.1104/pp.107.110981http://www.plantphysiol.org/content/146/2/623 – (On our blog : https://plantstomata.wordpress.com/2019/05/27/overexpression-of-atmyb44-enhances-stomatal-closure/ )

Jung J.-Y., Kim Y.-W., Kwak J. M., Hwang J.-U., Young J., Schroeder J. I., Hwang I., Lee Y. (2002) – Phosphatidylinositol 3- and 4-phosphate are required for normal stomatal movements. – Plant Cell 14: 2399–2412 – (On our blog : https://plantstomata.wordpress.com/2016/07/05/pi3p-and-pi4p-play-an-important-role-in-the-modulation-of-stomatal-movements/)

Juárez-Lopez, F. J., Escudero A., Mediavilla S. (2008) – Ontogenetic changes in stomatal and biochemical limitations to photosynthesis of two co-occurring Mediterranean oaks differing in leaf life span – Tree Physiology 28: 367–374 – https://doi.org/10.1093/treephys/28.3.367 –https://academic.oup.com/treephys/article/28/3/367/1655251 – (On our blog : https://plantstomata.wordpress.com/2019/03/16/ontogenetic-changes-in-stomatal-and-biochemical-limitations-to-photosynthesis/ )

Juhrbandt J., Leuschner C., Hölscher D. (2004) – The relationship between maximal stomatal conductance and leaf traits in eight Southeast Asian early successional tree species – Forest Ecol Management 202: 245–256 – https://doi.org/10.1016/j.foreco.2004.07.021https://www.sciencedirect.com/science/article/pii/S0378112704005389 – (On our blog : https://plantstomata.wordpress.com/2019/03/16/leaf-size-might-be-a-good-predictor-for-maximal-stomatal-conductance-2/ )

Julius-Maximilians-Universität Würzburg (2019) – How plants learned to save water – Phys.Org. FEBRUARY 21, 2019 – https://phys.org/news/2019-02-how-plants-learned-to-save.html – (On our blog : https://plantstomata.wordpress.com/2019/08/10/80028/ )

Jumrani K., Bhatia V. S., Pandey G. P. (2017) – Impact of elevated temperatures on specific leaf weight, stomatal density, photosynthesis and chlorophyll fluorescence in soybean – Photosynth Res. 131(3): 333-350 – doi: 10.1007/s11120-016-0326-y – Epub 2016 Dec 26 – https://www.ncbi.nlm.nih.gov/pubmed/?term=Bhatia+stomata – (On our blog : https://plantstomata.wordpress.com/2020/01/06/impact-of-elevated-temperatures-on-specific-leaf-weight-and-stomatal-density/ )

Jung C., Seo J. S., Han S. W., Koo Y. J., Kim C. H., Song S. I., Nahm B. H., Choi Y. D., Cheong J.-J. (2007) – Overexpression of AtMYB44 enhances stomatal closure to confer abiotic stress tolerance in transgenic Arabidopsis – Plant Physiol. 146: 623–635 – https://doi.org/10.1104/pp.107.110981http://www.plantphysiol.org/content/146/2/623 – (On our blog : https://plantstomata.wordpress.com/2020/03/07/overexpression-of-atmyb44-enhances-stomatal-closure-2/ )

Jung J.‐Y., Kim Y.‐W., Kwak J.M., Hwang J.‐U., Young J., Schroeder J. I., Hwang I., Lee Y. ( 2002) – Phosphatidylinositol 3‐ and 4‐phosphate are required for normal stomatal movements – The Plant Cell 14: 2399– 2412 – https://doi.org/10.1105/tpc.004143http://www.plantcell.org/content/14/10/2399 – (On our blog : https://plantstomata.wordpress.com/2019/04/02/pi3p-and-pi4p-play-an-important-role-in-the-modulation-of-stomatal-closing/ )

Jung P. K., Scott H. D. (1980) – Leaf water potential, stomatal resistance, and temperature relations in field-grown soybeans – Agron. J. 72: 986-990 –

Jurca M., Sjölander J., Ibáñez C., Matrosova A., Johansson , Kozarewa I., Takata N., Bakó L., Webb A. A. R., Israelsson M., Eriksson M. E. (2022) – ZEITLUPE Promotes ABA-Induced Stomatal Closure in Arabidopsis and Populus – Frontiers in Plant Science 13 – DOI: 10.3389/fpls.2022.829121https://www.researchgate.net/publication/358967274_ZEITLUPE_Promotes_ABA-Induced_Stomatal_Closure_in_Arabidopsis_and_Populus – (On our blog : https://plantstomata.wordpress.com/2022/03/27/zeitlupe-ztl-a-blue-light-photoreceptor-and-clock-component-regulates-aba-induced-stomatal-closure/ )

Jurczyk B., Grzesiak M., Pociecha E., Wlazło M., Rapacz M., (2019) – Diverse Stomatal Behaviors Mediating Photosynthetic Acclimation to Low Temperatures in Hordeum vulgare – Frontiers in Plant Science 09 January 2019 – https://doi.org/10.3389/fpls.2018.01963https://www.frontiersin.org/articles/10.3389/fpls.2018.01963/full – (On our blog : https://plantstomata.wordpress.com/2020/01/04/diverse-stomatal-behaviors-mediating-photosynthetic-acclimation-to-low-temperatures/ )

Jurczyk B., Janowiak F., Rapacz M.,  (    ) – Variation in waterlogging-triggered stomatal behavior contributes to changes in the cold acclimation process in prehardened Lolium perenne and Festuca pratensis – https://www.academia.edu/29446157/Variation_in_waterlogging-triggered_stomatal_behavior_contributes_to_changes_in_the_cold_acclimation_process_in_prehardened_Lolium_perenne_and_Festuca_pratensis – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/64806)

Jurenic I. (2016) – Natural variation in stomatal responsiveness of Arabidopsis thaliana plants grown at high and moderate relative humidity (MSc thesis) – Wageningen University & Research – https://www.wur.nl/en/article/Natural-variation-in-stomatal-responsiveness-of-Arabidopsis-thaliana-plants-grown-at-high-and-moderate-relative-humidity..htm – (On our blog : https://plantstomata.wordpress.com/2018/01/24/humidity-and-stomatal-responsiveness/ )

Karabourniotis G., Tzobanoglou D., Nikolopoulos D., Liakopoulos G. (2001) – Epicuticular Phenolics Over Guard Cells: Exploitation for in situ Stomatal Counting by Fluorescence Microscopy and Combined Image Analysis – Annals of Botany 87(5): 631–639 – https://doi.org/10.1006/anbo.2001.1386https://academic.oup.com/aob/article/87/5/631/2588449/ – (On our blog : https://plantstomata.wordpress.com/2019/10/08/in-situ-stomatal-counting-by-fluorescence-microscopy-and-combined-image-analysis-3/ )

Kagan M. L., Novoplansky N., Sachs T. (1991) – Variable cell lineages form the functional pea epidermis – Annals of Botany 69: 303–312 –  https://doi.org/10.1093/oxfordjournals.aob.a088346 –https://academic.oup.com/aob/article-abstract/69/4/303/172678?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2019/03/16/an-intracellular-program-which-generates-stomatal-patterns-during-rather-than-preceding-development/ )

Kagan M. L., Novoplansky N., Sachs T. (1992)Variable cell lineages during the formation of stomatal patterns – Annals of Botany 69: 303-312 –

Kaiser E., Morales A., Harbinson J., Heuvelink E., Marcelis L. F. M. (2020) – High Stomatal Conductance in the Tomato Flacca Mutant Allows for Faster Photosynthetic Induction – Front. Plant Sci. 25 August 2020 – https://doi.org/10.3389/fpls.2020.01317https://www.frontiersin.org/articles/10.3389/fpls.2020.01317/full – (On our blog : https://plantstomata.wordpress.com/2021/11/08/high-stomatal-conductance-in-tomato-flacca-mutant-it-keeps-its-stomata-open-at-all-times-at-the-cost-of-reduced-water-use-efficiency/ )

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Kaiser H. (1999) – Die stomatäre Reaktion von Sambucus nigra und Aegopodium podagraria in Abhängigkeit von Licht und Luftfeuchte – PhD Thesis Christian-Albrechts-Universität zu Kiel 129 pp. – https://macau.uni-kiel.de/servlets/MCRFileNodeServlet/dissertation_derivate_00000359/d359.pdf – (On our blog : https://plantstomata.wordpress.com/2018/03/27/die-stomatare-reaktion-in-abhangigkeit-von-licht-und-luftfeuchte/ )

Kaiser H. (2009) – The relation between stomatal aperture and gas exchange under consideration of pore geometry and diffusional resistance in the mesophyll – Plant, Cell and Environment 32: 1091–1098 – doi: 10.1111/j.1365-3040.2009.01990.x – https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-3040.2009.01990.x – (On our blog : https://plantstomata.wordpress.com/2018/09/22/the-relation-between-stomatal-aperture-and-gas-exchange/ )

Kaiser H., Eckstein J., Beyschlag W., Kappen L. (1999) – Variabilität stomatärer Aperturen bei Auftreten fleckenhafter Chlorophyllfluoreszenz – Bielefelder Ökologische Beiträge 14: 246–252 –

Kaiser H., Grams T. E. E. (2006) – Rapid hydropassive opening and subsequent active stomatal closure follow heat-induced electrical signals in Mimosa pudica – Journal of Experimental Botany 57(9): 2087–2092 – https://doi.org/10.1093/jxb/erj165https://academic.oup.com/jxb/article/57/9/2087/623683 – (On our blog : https://plantstomata.wordpress.com/2019/10/19/stomatal-movements-can-be-induced-by-electrical-signals/ )

Kaiser H., Kappen L. (1997) – In situ observations of stomatal movements in different light‐dark regimes: the influence of endogenous rhythmicity and long‐term adjustments – Journal of Experimental Botany 48: 1583–1589 – https://doi.org/10.1093/jxb/48.8.1583 –https://academic.oup.com/jxb/article/48/8/1583/501886 – (On our blog : https://plantstomata.wordpress.com/2019/02/11/the-influence-of-endogenous-rhythmicity-and-long%e2%80%90term-adjustments-on-stomatal-movements/ )

Kaiser H., Kappen L. (2000) – In-situ-observation of stomatal movements and gas exchange of Aegopodium podagraria L. in the understorey – Journal of Experimental Botany 51: 1741–1749 – DOI: 10.1093/jexbot/51.351.1741http://www.esalq.usp.br/lepse/imgs/conteudo_thumb/In-situ-observations-of-stomatal-movements-of-Glycyrrhiza-inflata-under-desert-conditions-of-Glycyrrhiza-inflata-under-desert-conditions.pdf – (On our blog : https://plantstomata.wordpress.com/2019/03/16/76380/ )

Kaiser H., Kappen L. (2001) – Stomatal oscillations at small apertures: indications for a fundamental imperfection of stomatal feedback-control inherent in the stomatal turgor mechanism – Journal of Experimental Botany 52: 1303–1313 – https://doi.org/10.1093/jexbot/52.359.1303 –https://academic.oup.com/jxb/article/52/359/1303/510917 – (On our blog : https://plantstomata.wordpress.com/2019/02/11/stomatal-oscillations-at-small-apertures/ )

Kaiser H. & Legner N. (2007) – Localization of mechanisms involved in hydropassive and hydroactive stomatal responses of Sambucus nigra to dry air – Plant Physiology 143: 1068–1077 – DOI: 10.1104/pp.106.089334https://www.ncbi.nlm.nih.gov/pubmed/17158586 – (On our blog : https://plantstomata.wordpress.com/2019/03/17/mechanisms-involved-in-hydropassive-and-hydroactive-stomatal-responses-to-dry-air/ )

Kaiser H., Paoletti E. (2014) – Dynamic stomatal changes. In: Tausz M, Grulke N (eds) Trees in a changing environment: ecophysiology, adaptation, and future survival – Springer, Dordrecht, Netherlands, pp 61–82.

Kakulas F., Evans J. R., Ludwig M., Veneklaas E. (2009) – Stomatal crypts may facilitate diffusion of CO2 to adaxial mesophyll cells in thick sclerophylls – Plant Cell and Environment 32(11):1596-611Doi: 10.1111/j.1365-3040.2009.02024.xhttps://www.researchgate.net/publication/26690884_Stomatal_crypts_may_facilitate_diffusion_of_CO2_to_adaxial_mesophyll_cells_in_thick_sclerophylls – (On our blog : https://plantstomata.wordpress.com/2019/08/06/stomatal-crypts-may-facilitate-diffusion-of-co2/ )

Kala J., De Kauwe M. G., Pitman A. J., Lorenz R., Medlyn B. E., Wang Y. -P., Lin Y. -S., Abramowitz G., (2015) – Implementation of an optimal stomatal conductance scheme in the Australian Community Climate Earth Systems Simulator (ACCESS1.3b) – DOI:10.5194/gmd-8-3877-2015https://ui.adsabs.harvard.edu/abs/2015GMD…..8.3877K/abstract (On our blog : https://plantstomata.wordpress.com/2020/10/25/an-optimal-stomatal-conductance-scheme-in-the-australian-community-climate-earth-systems-simulator/ )

Kala J., De Kauwe M. G., Pitman A. J., Medlyn B. E., Wang Y.-P., Lorenz R., Perkins-Kirkpatrick S. E. (2016) – Impact of the representation of stomatal conductance on model projections of heatwave intensity – Scientific Reports 6, Article number: 23418 – doi: 10.1038/srep23418 – https://www.nature.com/articles/srep23418 – (On our blog : https://plantstomata.wordpress.com/2019/03/26/impact-of-the-representation-of-stomatal-conductance-on-model-projections-of-heatwave-intensity/ )

Kalariya K. A., Mehta D., Goswami N., Singh A. L., Chakraborty K., Mahatma M. K., Zala P. V., Patel C. B. (2017) – Stomatal clustering pattern in Arachis hypogea L. under water deficit stress – Indian J. Experim. Biol. 55:880-883 – http://nopr.niscair.res.in/bitstream/123456789/43225/1/IJEB%2055%2812%29%20880-883.pdf – (On our blog : https://plantstomata.wordpress.com/2022/02/28/stomatal-clustering-pattern-under-water-deficit-stress/ )

Kalariya K. A., Shahi D., Singh A. L., Roy S. (2021) – Stomatal Development and Impact of Stomatal Movement on Secondary Metabolism in Medicinal Plants – JSM Environmental Science & Ecology 9(1): 1074 – https://www.jscimedcentral.com/EnvironmentalScience/environmentalscience-9-1074.pdf – (On our blog : https://plantstomata.wordpress.com/2022/02/28/formation-of-stomata-is-under-strict-genetic-control-but-is-governed-greatly-by-the-conditions-like-temperature-light-pathogens-etc/ )

Kale L., Nakurte I., Jalakas P., Kunga-Jegere L., Brosché M., Rostoks N. (2019) – Arabidopsis mutant dnd2 exhibits increased auxin and abscisic acid content and reduced stomatal conductance – Plant Physiol Biochem. 140: 18-26 – doi: 10.1016/j.plaphy.2019.05.004 – Epub 2019 May 3 -PMID: 31078052 – https://pubmed.ncbi.nlm.nih.gov/31078052/ – (On our blog : https://plantstomata.wordpress.com/2021/01/27/arabidopsis-dnd2-mutant-exhibited-aba-overaccumulation-and-stomatal-phenotypes-which-may-contribute-to-the-observed-improvement-in-drought-stress-resistance/ )

Kalliola M., Jakobson L., Davidsson P., Pennanen V., Waszczak C., Yarmolinsky D., Zamora O., Tapio Palva E., Kariola T., Kollist H., Brosché M. (2019) – The role of strigolactones in regulation of stomatal conductance and plant-pathogen interactions in Arabidopsis thaliana – biorxiv – doi: https://doi.org/10.1101/573873https://www.biorxiv.org/content/10.1101/573873v2 – (On our blog : https://plantstomata.wordpress.com/2019/03/21/the-role-of-strigolactones-in-regulation-of-stomatal-conductance/ )

Kalliola M., Jakobson L., Davidsson P., Pennanen V., Waszczak C., Yarmolinsky D., Zamora O., Tapio Palva E., Kariola T., Kollist H., Brosché M. (2020) – Differential role of MAX2 and strigolactones in pathogen, ozone, and stomatal responses – Plant Direct 4: e00206 – doi: 10.1002/pld3.206https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047155/ – (On our blog : https://plantstomata.wordpress.com/2020/12/31/differential-role-of-max2-and-strigolactones-in-pathogen-ozone-and-stomatal-responses/ )

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Kamakura M., Kosugi Y., Takanashi S., Matsumoto K., Okumura M., Philip E. (2011) – Patchy stomatal behavior during midday depression of leaf CO₂ exchange in tropical trees – Tree Physiology 31(2): 160-168 – DOI:10.1093/treephys/tpq102 –https://www.semanticscholar.org/paper/Patchy-stomatal-behavior-during-midday-depression-Kamakura-Kosugi/a534b058ab8042d8c5fad92a719fb4b13b08c668 – (On our blog : https://plantstomata.wordpress.com/2019/03/15/patchy-stomatal-behavior-during-midday-depression-of-leaf-co%e2%82%82-exchange/ )

Kamakura M., Kosugi Y., Takanashi S., Tobita H., Uemura A., Utsugi H. (2012) – Observation of the scale of patchy stomatal behavior in leaves of Quercus crispula using an Imaging-PAM chlorophyll fluorometer – Tree Physiology 32: 839-846 – doi: 10.1093/treephys/tps053https://www.academia.edu/18409128/Observation_of_the_scale_of_patchy_stomatal_behavior_in_leaves_of_Quercus_crispula_using_an_Imaging-PAM_chlorophyll_fluorometer?auto=download – (On our blog : https://plantstomata.wordpress.com/2019/11/20/the-spatial-scale-of-stomatal-patches/ )

Kamakura M., Kosugi Y., Takanashi S., Uemura A., Utsugi H., Kassim A. R. (2018) – Occurrence of stomatal patchiness and its spatial scale in leaves from various sizes of trees distributed in a south-east asian tropical rainforest in peninsular Malaysia – Tree Physiol. 35: 61–70 – doi: 10.1093/treephys/tpu109https://academic.oup.com/treephys/article/35/1/61/1675621 – (On our blog : https://plantstomata.wordpress.com/2019/12/10/stomatal-patchiness-and-its-spatial-scale-in-leaves-from-various-sizes-of-trees/ )

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Kammer P. M., Steiner J. S., Schöb C. (2015) – Arabis alpina and Arabidopsis thaliana have different stomatal development strategies in response to high altitude pressure conditions – Alpine Botany, 125(2): 101-112 – http://doi.org/10.5167/uzh-112101 – http://www.zora.uzh.ch/112101/– (On our blog : https://plantstomata.wordpress.com/2016/08/04/17522/)

Kamrani Y. Y., Shomali A., Aliniaeifard S., Oksana Lastochkina O., Moosavi-Nezhad M., Nima Hajinajaf N., Talar U. (2022) – Regulatory Role of Circadian Clocks on ABA Production and Signaling, Stomatal Responses, and Water-Use Efficiency under Water-Deficit Conditions – MDPI Cells 11(7): 1154 – https://doi.org/10.3390/cells11071154https://www.mdpi.com/2073-4409/11/7/1154 – (On our blog : https://plantstomata.wordpress.com/2022/04/19/the-circadian-clock-through-aba-directs-plants-to-modulate-their-stomatal-responses-and-feedback-mechanisms-to-ensure-survival-and-to-enhance-their-fitness-under-drought-conditions/ )

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Kang X., Xu G., Lee B., Chen C., Zhang H., Kuang R., Ni M. (2018) – HRB2 and BBX21 interaction modulates Arabidopsis ABI5 locus and stomatal aperture – Plant, Cell & Environment – Online Version of Record  – https://doi.org/10.1111/pce.13336 – https://onlinelibrary.wiley.com/doi/pdf/10.1111/pce.13336 – (On our blog : https://plantstomata.wordpress.com/2018/05/28/two-light-signalling-proteins-repress-aba-signalling-to-sustain-gas-exchange-during-periodic-drought/ )

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Kangur O., Steppe K., Schreel J., von der Crone J., Sellin A. (2021) – Variation in nocturnal stomatal conductance and development of predawn disequilibrium between soil and leaf water potentials in nine temperate deciduous tree species – FUNCTIONAL PLANT BIOLOGY 48(5): 483–492 – https://doi.org/10.1071/FP20091https://biblio.ugent.be/publication/8704400 – (On our blog : https://plantstomata.wordpress.com/2021/07/23/how-nocturnal-stomatal-conductance-differs-among-potted-saplings-in-wet-and-dry-soil-conditions/ )

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Karanam A., He D., Hsu P.-K., Schulze S., Dubeaux G., Karmakar R., Schroeder J. I., Rappel W.-J. (2021) – Boolink: a graphical interface for open access Boolean network simulations and use in guard cell CO2 signaling – Plant Physiology – DOI: 10.1093/plphys/kiab344https://www.researchgate.net/publication/353789953_Boolink_a_graphical_interface_for_open_access_Boolean_network_simulations_and_use_in_guard_cell_CO2_signaling – (On our blog : https://plantstomata.wordpress.com/2021/08/16/boolink-used-in-guard-cell-co2-signaling/ )

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Kelly G., Lugassi N., Belausov E., Wolf D., Khamaisi B., Brandsma D., Kottapalli J., Fidel L., Ben-Zvi B., Egbaria A., Acheampong A. K., Zheng C., Or E., Distelfeld A., David-Schwartz R., Carmi N., Granot D. (2017) – The Solanum tuberosum KST1 partial promoter as a tool for guard cell expression in multiple plant species – J Exp Bot. 68(11): 2885-2897 – doi: 10.1093/jxb/erx159 – PMID: 28531314 – PMCID: PMC5853950 – https://pubmed.ncbi.nlm.nih.gov/28531314/ – (On our blog : https://plantstomata.wordpress.com/2021/06/29/kst1ppro-can-be-used-to-drive-constitutive-guard-cell-expression-in-monocots-and-dicots/ )

Kelly G., Moshelion M., David-Schwartz R., Halperin O., Wallach R., Attia Z.Belausov E., Granot D. (2013) – Hexokinase mediates stomatal closure – Plant Journal 75: 977988 (2013)  – doi: 10.1111/tpj.12258 – https://www.infona.pl/resource/bwmeta1.element.wiley-tpj-v-75-i-6-tpj12258 – (On our blog: https://plantstomata.wordpress.com/2017/10/22/surplus-sucrose-is-carried-toward-the-stomata-by-the-transpiration-stream-and-stimulates-stomatal-closure-via-hxk/)

Kelly W. B., Esser J. E., Schroeder J. I. (1995) – Effects of cytosolic calcium and limited, possible dual, effects of G protein modulators on guard cell inward potassium channels – Plant J. 8:479–489 – (On our blog : https://plantstomata.wordpress.com/2016/07/05/cytosolic-calciumg-protein-modulators-and-stomata/)

Kennard J. L., Cleary A. L. (1997) – Pre-mitotic nuclear migration in subsidiary mother cells of Tradescantia occurs in G1 on the cell cycle and requires F-actin – Cell Motility and Cytoskeleton 36: 55–67 – https://doi.org/10.1002/(SICI)1097-0169(1997)36:1<55::AID-CM5>3.0.CO;2-G –https://onlinelibrary.wiley.com/doi/abs/10.1002/%28SICI%291097-0169%281997%2936%3A1%3C55%3A%3AAID-CM5%3E3.0.CO%3B2-G – (On our blog : https://plantstomata.wordpress.com/2019/04/29/pre-mitotic-nuclear-migration-in-subsidiary-mother-cells-of-stomata/ )

Kenzo T., Yoneda R., Sano M., Araki M., Shimizu A., Tanaka-Oda A., Chann S. (2012) – Variations in Leaf Photosynthetic and Morphological Traits with Tree Height in Various Tree Species in a Cambodian Tropical Dry Evergreen Forest – Japan Agricultural Research Quarterly: JARQ 46(2): 167-180 – ISSN:0021-3551 – (https://www.jstage.jst.go.jp/article/jarq/46/2/46_2_167/_pdf) – (On our blog : https://plantstomata.wordpress.com/2015/04/16/stomata-and-tree-height/)

Kereston R. (2022) – Stomata Molecular Switches and the Future of Agriculture with Dr. Sixue Chen – University of Florida/Genetics Institute – https://biotech.ufl.edu/stomata-molecular-switches-and-the-future-of-agriculture-with-dr-sixue-chen/https://express.adobe.com/page/O29V2vHgAwcej/ – (On our blog : https://plantstomata.wordpress.com/2022/03/15/stomata-molecular-switches/ )

Kerl H. W. (1929) – Beitrag zur Kenntnis der Spaltöffnungsbewegung – Planta 9: 407-463 –

Kerr P. S., Rufty T. W., Huber S. C. (1985) – Endogenous rhythms in photosynthesis, sucrose phosphate synthase activity, and stomatal resistance in leaves of soybean (Glycine max L. Merr.) – Plant Physiol. 77: 275–280 – DOI: 10.1104/pp.77.2.275https://www.ncbi.nlm.nih.gov/pubmed/16664041?dopt=Abstract – (On our blog : https://plantstomata.wordpress.com/2019/09/21/endogenous-rhythms-in-photosynthesis-sucrose-phosphate-synthase-activity-and-stomatal-resistance/ )

Kerstiens G. (1996) – Diffusion of water vapour and gases across cuticles and through stomatal pores presumed closed – In: Kerstiens, G. (ed.): Plant Cuticles – An Integrated Functional Approach. Pp. 121-134 – BIOS Scientific Publishers, Oxford 1996

Kerstiens G. (1996) –  Cuticular water permeability and its physiological significance – Journal of Experimental Botany 47(305): 1813-1832 – https://www.jstor.org/stable/23695572 – (On our blog : https://plantstomata.wordpress.com/2022/02/06/contrasting-evidence-for-an-interaction-between-cuticular-transpiration-and-stomatal-sensitivity-to-air-humidity-is-presented/ )

Kerstiens G. (1997) – In vivo manipulation of cuticular water permeance and its effect on stomatal response to air humidity – New Phytologist 137: 473–480 – https://doi.org/10.1046/j.1469-8137.1997.00847.xhttps://nph.onlinelibrary.wiley.com/doi/abs/10.1046/j.1469-8137.1997.00847.x – (On our blog : https://plantstomata.wordpress.com/2019/04/29/cuticular-water-permeance-and-its-effect-on-stomatal-response-to-air-humidity/ )

Kerstiens G., Tych W., Robinson M. F., Mansfield T. A. (2002) Sodium-related partial stomatal closure and salt tolerance of Aster tripolium – New Phytologist 153(3): 509-515 – http://onlinelibrary.wiley.com/doi/10.1046/j.0028-646X.2001.00330.x/full – (On our blog : https://plantstomata.wordpress.com/2016/07/05/na-stomata-and-salt-tolerance/)

Ketellapper H. J. (1959) – The mechanism of stomatal movement – Amer. Jour. Bot.  46(3): 225-231 – (On our blog : https://plantstomata.wordpress.com/2017/03/24/stomatal-movement-mechanism/)

Ketellapper H. J. (1963) – Stomatal physiology – Annual Rev. Pl. Physiol. 14: 249-270 – https://doi.org/10.1146/annurev.pp.14.060163.001341 – https://www.annualreviews.org/doi/abs/10.1146/annurev.pp.14.060163.001341?journalCode=arplant.1 – (On our blog : https://plantstomata.wordpress.com/2018/04/30/stomatal-physiology-2/  )

Keys S. C. (1976) – Stomatal activity patterns of Provenance plantations of Abies concolor and Abies grandisMSci Thesis – file:///C:/Users/wille/Downloads/KeysStevenC1977%20(2).pdf – (On our blog : https://plantstomata.wordpress.com/2021/10/15/stomatal-activity-patterns-of-provenance-plantations/ )

Khalil A. M., Grace J. (1993) – Does xylem sap ABA control the stomatal behaviour of water stressed Sycamore (Acer pseudoplatanus L.) seedlings? – Journal of Experimental Botany 44: 1127-1134 – https://doi.org/10.1093/jxb/44.7.1127 –https://academic.oup.com/jxb/article-abstract/44/7/1127/480326?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2019/02/04/does-xylem-sap-aba-control-the-stomatal-behaviour/ )

Khan A., Zheng J., Tan D. K. Y., Khan A., Akhtar K., Kong X., Munsif F., Iqbal A., Afridi M. Z., Ullah A., Fahad S., Zhou R. (2019) – Changes in Leaf Structural and Functional Characteristics when Changing Planting Density at Different Growth Stages Alters Cotton Lint Yield under a New Planting Model – Agronomy 9(12): 859- https://doi.org/10.3390/agronomy9120859https://www.mdpi.com/2073-4395/9/12/859/htm – (On our blog : https://plantstomata.wordpress.com/2021/09/18/changes-in-leaf-structural-and-functional-characteristics-of-different-cotton-varieties-in-order-to-change-the-planting-densities-to-improve-lint-yield-under-a-new-planting-model/ )

Khan F., Yousaf Z., Ahmed H. S., Arif A., Rehman H. A., Younas A., Rashid M., Tariq Z., Raiz N. (2014) – Stomatal Patterning: An Important Taxonomic Tool for Systematical Studies of Tree Species of Angiosperm – Annual Research & Review in Biology 4(24): 4034-4053 – http://www.journalrepository.org/media/journals/ARRB_32/2014/Jul/Khan4242014ARRB10073_1.pdf – (On our blog : https://plantstomata.wordpress.com/2017/11/08/stomatal-patterning-as-an-important-taxonomic-tool/)

Khan M., Rozhon W., Bigeard J., Pflieger D., Husar S., Pitzschke A., Teige M., Jonak C., Hirt H., Poppenberger B. (2013) – Brassinosteroid-regulated GSK3/Shaggy-like Kinases phosphorylate mitogen-activated protein (MAP) Kinase Kinases, which control stomata development in Arabidopsis thaliana – Journal of Biological Chemistry 288: 75197527 – doi:10.1074/jbc.M112.384453 – http://www.jbc.org/content/288/11/7519.full – (On our blog : https://plantstomata.wordpress.com/2018/04/23/bin2-phosphorylates-mkk4-which-inhibits-its-activity-against-mpk6-in-a-mapk-module-that-controls-stomata-patterning/

Khan P. S. S. V., Kozai T., Nguyen Q. T., Kubota C., Dhawan V. (2003) – Growth and Water Relations of Paulownia fortunei Under Photomixotrophic and Photoautotrophic Conditions – Biologia Plantarum 46:161–166 – https://doi.org/10.1023/A:1022844720795https://link.springer.com/article/10.1023%2FA%3A1022844720795#citeas – (On our blog : https://plantstomata.wordpress.com/2020/02/17/stomata-and-photomixotrophic-and-photoautotrophic-conditions/ )

Khan R., Rehman F., Gulafshan, Khan A., (2020) – Effect of salinity (Na2SO4) on stomata, and yield parameters of Indian mustard (Brassica juncea L) var. Goldi – Int J Nanomater Nanotechnol Nanomed 6(2): 021-023 – DOI: 10.17352/2455-3492.000036https://www.peertechzpublications.com/articles/IJNNN-6-136.php – (On our blog : https://plantstomata.wordpress.com/2021/02/03/due-to-salinity-levels-stomata-become-destroyed-without-showing-any-damage-of-physiological-characters/ )

Khanna R., Li J., Tseng T.-S., Schroeder J. I., Ehrhardt D. W., Briggs W.R. (2014) – COP1 Jointly modulates cytoskeletal processes and electrophysiological responses required for stomatal closure – Mol. Plant. 7: 1441–1454 – https://www.cell.com/molecular-plant/pdf/S1674-2052(14)60947-3.pdf – (On our blog : https://plantstomata.wordpress.com/2022/03/03/cop1-is-revealed-as-a-potential-coordinator-of-cytoskeletal-and-electrophysiological-activities-required-for-stomatal-guard-cell-function/ )

Khatoon S., Majid S. A., Bibi A., Javed G., Ulfat A. (2016) – Yield stability evaluation of wheat (Triticum aestivum L.) cultivated on different environments of district Poonch (AJK) Pakistan based upon water-related parameters – International Journal of Agronomy and Agricultural Research (IJAAR) 8(4): 11-21 – ISSN: 2223-7054 –
https://www.researchgate.net/publication/319954996_Yield_stability_evaluation_of_wheat_Triticum_aestivum_L_cultivated_on_different_environments_of_district_Poonch_AJK_Pakistan_based_upon_water-related_parameters – (On our blog : https://plantstomata.wordpress.com/2020/03/22/the-more-thermostable-genotypes-holding-an-optimum-relative-water-content-and-more-stomatal-size-and-frequency-had-more-biological-yield/ )

Khazaei H., Mohammady S., Monneveux P., Stoddard F. (2011) – Determination of direct and indirect effects of carbon isotope discrimination (∆), stomatal characteristics and water use efficiency on grain yield in wheat using sequential path analysis – Australian Journal of Crop Sciences 5(4): 466-472 – https://researchportal.helsinki.fi/en/publications/determination-of-direct-and-indirect-effects-of-carbon-isotope-di – (On our blog : https://plantstomata.wordpress.com/2020/07/05/85021/ )

Khazaei H., Monneveux P., Hongbo S., Mohammady S. (2010) – Variation for stomatal characteristics and water use efficiency among diploid, tetraploid and hexaploid Iranian wheat landraces. Genet. Resour. Crop Evol. 57: 307-314 – http://link.springer.com/article/10.1007%2Fs10722-009-9471-x – (On our blog : https://plantstomata.wordpress.com/2016/02/16/water-use-efficiency-and-stomatal-characteristics/ ).

Khazaei H., O’Sullivan, Silanpää M. J., Stoddard F. L. (2014)  Use of synteny to identify candidate genes underlying QTL controlling stomatal traits in faba bean (Vicia faba L.) – Theor Appl Genet. 127(11): 2371–2385 –DOI: 10.1007/s00122-014-2383-y – https://www.researchgate.net/publication/265342275_Use_of_synteny_to_identify_candidate_genes_underlying_QTL_controlling_stomatal_traits_in_faba_bean_Vicia_faba_L – (On our blog : https://plantstomata.wordpress.com/2016/11/16/synteny-and-identification-of-candidate-genes-underlying-qtl-controlling-stomatal-traits/ )

Khazaei H., Street K., Santanen A., Bari A., Stoddard F. L. (2013) – Do faba bean (Vicia faba L.) accessions from environments with contrasting seasonal moisture availabilities differ in stomatal characteristics and related traits? – Genet. Resour. Crop Evol. 60: 23-43 – doi:10.1007/s10722-013-0002-46363 – http://link.springer.com/article/10.1007%2Fs10722-013-0002-4 – (On our blog : https://plantstomata.wordpress.com/2016/11/16/stomatal-characteristics-and-the-environment/ )

Khokon M. A. R., Hossain M. A., Munemasa S., Uraji M., Nakamura Y., Mori I. C., Murata Y. (2010) – Yeast elicitor-induced stomatal closure and peroxidase- mediated ROS production in Arabidopsis – Plant Cell Physiol. 51: 1915–1921 – doi: 10.1093/pcp/pcq145 – https://www.ncbi.nlm.nih.gov/pubmed/20876608 – (On our blog : https://plantstomata.wordpress.com/2018/04/23/yel-induces-stomatal-closure-accompanied-by-ros-production-mediated-by-peroxidases-and-no-production/ )

Khokon M., Jahan M. S., Rahman T., Hossain M. A., Muroyama D., Minami I., Munemasa S, Mori I. C., Nakamura Y, Murata Y.(2011) – Allyl isothiocyanate (AITC) induces stomatal closure in Arabidopsis. – Plant Cell Environ. 34: 1900–1906 – doi: 10.1111/j.1365-3040.2011.02385.x – https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1365-3040.2011.02385.x – (On our blog : https://plantstomata.wordpress.com/2018/04/24/aitc-induces-stomatal-closure/ )

Khokon M. A. R., Okuma E., Hossain M. A., Munemasa S., Uraji M., Nakamura Y., Mori I. C., Murata Y. (2011) – Involvement of extracellular oxidative burst in salicylic acid-induced stomatal closure in Arabidopsis – Plant Cell Environ. 34: 434–443 – doi: 10.1111/j.1365-3040.2010.02253.x  – (On our blog :  https://plantstomata.wordpress.com/2016/07/06/salicylic-acid-induced-stomatal-closure/)

Khokon M. A. R., Salam M. A., Jammes F., Ye W., Hossain M. A., Uraji M., Nakamura Y., Mori I. C., Kwak J. M., Murata Y. (2015) – Two guard cell MAPKs, MPK9 and MPK12, function in methyl jasmonate-induced stomatal closure in Arabidopsis thaliana – Plant Biology (Stuttg) 17: 946–952 – doi: 10.1111/plb.12321 –  (https://plantstomata.wordpress.com/page/11/). – (On our blog : https://plantstomata.wordpress.com/2015/02/19/stomatal-closure-in-arabidopsis-thaliana/ ).

Khokon M. A. R.,  Salam M. A., Jammes F., Ye W., Hossain M. A., Okuma E., Nakamura Y., Mori I. C., Kwak J. M., Murata Y. (2017) – MPK9 and MPK12 function in SA-induced stomatal closure in Arabidopsis thaliana – Bioscience Biotechnology and Biochemistry 81(7):1-7 – DOI: 10.1080/09168451.2017.1308244 – https://www.researchgate.net/publication/315826548_MPK9_and_MPK12_function_in_SA-induced_stomatal_closure_in_Arabidopsis_thaliana – (On our blog : https://plantstomata.wordpress.com/2018/08/14/mpk9-and-mpk12-are-positive-regulators-of-sa-signaling-in-stomata/ )

Khokon M. A. R., Uraji M., Munemasa S., Okuma E., Nakamura Y., Mori I. C., et al. (2010) – Chitosan-induced stomatal closure accompanied by peroxidase- mediated reactive oxygen species production in Arabidopsis – Biosci. Biotechnol. Biochem. 74: 2313–2315 – doi: 10.1271/bbb.100340 – https://www.ncbi.nlm.nih.gov/pubmed/21071853 – (On our blog : https://plantstomata.wordpress.com/2018/05/02/chitosan-induces-ros-production-mediated-by-peroxidase-resulting-in-stomatal-closure/ )

Khorsgani O. A., Flores F. B., PessarakliM. (2018) – Plant signaling pathways involved in stomatal movement under drought stress conditions ) – Advances in Plants & Agriculture Research 8 (3) : EISSN: 2373-6402 – https://medcraveonline.com/APAR/plant-signaling-pathways-involved-in-stomatal-movement-under-drought-stress-conditions.html -(On our blog : https://plantstomata.wordpress.com/2020/12/10/improved-stomatal-responses-under-various-environmental-conditions-particularly-stress-conditions-and-specifically-drought-stress/ )

Kiani-Pouya A., Rasouli F., Rabbi B., Falakboland Z., Yong M., Chen Z.-H., Zhou M., Shabala S. (2020) – Stomatal traits as a determinant of superior salinity tolerance in wild barley – Journal Plant Physiology 245: – https://doi.org/10.1016/j.jplph.2019.153108 –https://www.sciencedirect.com/science/article/pii/S0176161719302378 – (On our blog : https://plantstomata.wordpress.com/2020/05/11/stomatal-traits-and-superior-salinity-tolerance/ )

Kilic S. (2009) –  Anatomical and Pollen Characters in the Silene L. (Caryophyllaceae) from Turkey – Botany Research Journal 2: 34-44 – http://medwelljournals.com/abstract/?doi=brj.2009.34.44  – (On our blog : https://plantstomata.wordpress.com/2018/03/27/stomata-in-the-silene-caryophyllaceae/ )

Kim C. Y. (2012) – Stomatal responses of C3 and C4 Cyperus species(Cyperaceae) in Korea to elevated CO2 concentration, M.S.D. Dissertation, Sungshin Women’s University, Seoul, Korea.

Kim D. J., Lee J. S. (2007) – Current theories for mechanism of stomatal opening: Influence of blue light: Mesophyll cells and sucrose – J. Plant Biol. 50: 523-556 – http://link.springer.com/article/10.1007%2FBF03030704 – (On our blog : https://plantstomata.wordpress.com/2016/02/16/mechanism-of-stomatal-opening/ )

Kim H. H., Goins G. D., Wheeler R. M., Sager J. C. (2004) – Stomatal conductance of lettuce grown under or exposed to different light qualities – Ann. Bot. 94(5): 691-697 – https://doi.org/10.1093/aob/mch192https://academic.oup.com/aob/article/94/5/691/151928 – (On our blog : https://plantstomata.wordpress.com/2020/09/08/stomatal-conductance-is-responsive-to-spectral-quality-during-growth/ )

Kim H., Lee S. J. (xxxx) – Stomata‐Inspired Membrane Produced Through Photopolymerization Patterning – Advanced Functional Materials 25(28): 4496 – 4505 – DOI: 10.1002/adfm.201501445 – https://www.infona.pl/resource/bwmeta1.element.wiley-adfm-v-25-i-28-adfm201501445 – (On our blog : https://plantstomata.wordpress.com/2017/10/10/a-stomata%e2%80%90inspired-membrane/)

Kim H., Lee S. J. (2016) – Fabrication of Triple-parted Stomata-inspired Membrane with Stimulus-responsive Functions – Sci Rep 6: 21258 – https://doi.org/10.1038/srep21258https://www.nature.com/articles/srep21258 – (On our blog : https://plantstomata.wordpress.com/2022/04/12/105293/ )

Kim H., Ridenour J. B., Dunkle L. D., Bluhm B. H. (2011) – Regulation of Stomatal Tropism and Infection by Light in Cercospora zeae-maydis: Evidence for Coordinated Host/Pathogen Responses to Photoperiod? –  PLoS Pathog 7(7): e1002113 – https://doi.org/10.1371/journal.ppat.1002113https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1002113 – (On our blog : https://plantstomata.wordpress.com/2022/02/03/a-novel-molecular-mechanism-underlying-stomatal-tropism-in-a-foliar-fungal-pathogen/ )

Kim J., Joo Y., Kyung J., Jeon M., Park J. Y., Lee H. G., Chung D. S., Lee E., Lee I. (2018) – A molecular basis behind heterophylly in an amphibious plant, Ranunculus trichophyllus – Science.gov (United States) – https://worldwidescience.org/topicpages/c/closing+plant+stomata.html# – (On our blog : https://plantstomata.wordpress.com/2022/03/06/in-terrestrial-leaves-of-ranunculus-trichophyllus-abi3-mediated-activation-of-the-adaxial-genes-rthd-zipiiis-and-stomagen-and-vdn7-established-leaf-polarity-and-stomata-and-vessel-develo/ )

Kim J., van Iersel M. W. (2008) – ABA drenches induce stomatal closure and prolong shelf life of Salvia splendens – Southern Nursery Assn. Res. Conf. 53: 107-111 – SNA Research Conference Vol. 53 – https://www.researchgate.net/profile/Marc_Van_Iersel2/publication/258514885_ABA_dreches_induce_stomatal_closure_and_prolong_shelf_life_of_Salvia_splendens/links/55c633c308aea2d9bdc5452f/ABA-dreches-induce-stomatal-closure-and-prolong-shelf-life-of-Salvia-splendens.pdf – (On our blog : https://plantstomata.wordpress.com/2020/12/09/aba-drenches-induce-stomatal-closure-and-prolong-shelf-life/ )

Kim J., Verma S. (1991) – Modelling canopy stomatal conductance in a temperate grassland ecosystem – Agric Forest Meteorol. 55: 149–166 – doi: 10.1016/0168-1923(91)90028-Ohttps://www.sciencedirect.com/science/article/pii/016819239190028O – (On our blog : https://plantstomata.wordpress.com/2019/05/06/modelling-canopy-stomatal-conductance/ )

Kim J.-H., Oh Y., Yoon H., Hwang I., Chang Y.-S. (2015) – Iron Nanoparticle-Induced Activation of Plasma Membrane H+-ATPase Promotes Stomatal Opening in Arabidopsis thaliana – Environ. Sci. Technol. 49(2): 1113–1119 – –https://doi.org/10.1021/es504375thttps://pubs.acs.org/doi/10.1021/es504375t – (On our blog : https://plantstomata.wordpress.com/2022/01/31/nzvi-enhances-stomatal-opening-by-inducing-the-activation-of-plasma-membrane-h-atpase/ )

Kim J. S., Jeong W. G., Sung M. W. (1987) – Effects of abscisic acid on the epidermal structure and ontogeny of stomata in Orostachys malacophyllus leaves -Korean Journal of Botany 30(1): 21-30 –
https://eurekamag.com/research/005/287/005287395.php – (On our blog : https://plantstomata.wordpress.com/2019/02/01/effects-of-aba-on-the-epidermal-structure-and-stomata/ )

Kim L., Balani S., Edelberg M., Macke N. (2021) – Effects of Various Environmental Factors on Stomatal Density, Area, and Potential Conductance Index – Journal of Emerging Investigators – www.emerginginvestigators.org – 4(1) – https://emerginginvestigators.org/articles/effects-of-various-environmental-factors-on-stomatal-density-area-and-potential-conductance-index/pdf – (On our blog : https://plantstomata.wordpress.com/2022/04/02/making-generalizations-about-the-impact-of-co2-in-combination-with-other-environmental-factors-is-risky/ )

Kim M., Hepler P. K., Eun S. O., Ha K. S., Lee Y. (1995) – Actin filaments in mature guard cells are radially distributed and involved in stomatal movement – Plant Physiol. 109: 1077–1084 – (On our blog https://plantstomata.wordpress.com/2016/07/06/microfilaments-participate-in-stomatal-aperture-regulation/ )

Kim S.-H., Lieth J. H. (2003) – A Coupled Model of Photosynthesis, Stomatal Conductance and Transpiration for a Rose Leaf (Rosa hybrida L.)  – Annals of Botany 91(4): 771-781 – https://doi.org/10.1093/aob/mcg080 –https://academic.oup.com/aob/article/91/7/771/177691 – (On our blog : https://plantstomata.wordpress.com/2019/03/22/a-coupled-model-of-photosynthesis-stomatal-conductance-and-transpiration/ )

Kim S. J., Hahn E. J., Heo J. W., Paek K. Y. (2004) – Effects of LEDs on net photosynthetic rate, growth and leaf stomata of Chrysantemum plantlets in vitro – Sci. Hort.  101: 143- 151 – https://doi.org/10.1016/j.scienta.2003.10.003 – (On our blog : https://plantstomata.wordpress.com/2018/04/24/effects-of-leds-on-stomata/ )

Kim T. H., Böhmer M., Hu H. H., Nishimura N., Schroeder J. I. (2010) – Guard cell signal transduction network: advances in understanding abscisic acid, CO2, and Ca2+ signaling – Annu. Rev. Plant Biol. 61: 561-591 – doi: 10.1146/annurev-arplant-042809-112226 – (On our blog : https://plantstomata.wordpress.com/2016/02/16/abscisic-acid-co2-and-ca2-signaling-in-stomata/).

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Knapp A. K., Smith W. K. (1988) – Effect of water stress on stomatal and photosynthetic responses in Subalpine plants to cloud patterns – America Journal of Botany 75: 851–858 – https://doi.org/10.1002/j.1537-2197.1988.tb13508.xhttps://bsapubs.onlinelibrary.wiley.com/doi/abs/10.1002/j.1537-2197.1988.tb13508.x – (On our blog : https://plantstomata.wordpress.com/2019/05/09/effect-of-water-stress-on-stomatal-responses-to-cloud-patterns/ )

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Knight R. C. (1922) – Further Observations on the Transpiration, Stomata, Leaf Water-content, and Wilting of Plants – Annals of Botany. Vol. XXXVL No. CXLIH: 361-383 – https://ia800708.us.archive.org/view_archive.php?archive=/28/items/crossref-pre-1923-scholarly-works/10.1093%252Foxfordjournals.aob.a089774.zip&file=10.1093%252Foxfordjournals.aob.a089812.pdf – (On our blog : https://plantstomata.wordpress.com/2022/03/02/further-observations-on-the-transpiration-stomata-leaf-water-content-and-wilting-of-plants/ )

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Kolbe A. R.Brutnell T. P.Cousins A. B.Studer A. J. (2018) – Carbonic Anhydrase Mutants in Zea mays Have Altered Stomatal Responses to Environmental Signals – Plant Physiol. 2018 – https://doi.org/10.1104/pp.18.00176 – http://www.plantphysiol.org/content/177/3/980 – (On our blog : https://plantstomata.wordpress.com/2018/07/16/ca-mediated-signaling-in-the-control-of-stomatal-movement-but-not-stomatal-development/ )

Kolbe A. R., Studer A. J., Cornejo O. E., Cousins A. B. (2019) – Insights from transcriptome profiling on the non-photosynthetic and stomatal signaling response of maize carbonic anhydrase mutants to low CO2 – BMC Genomics 20, Article number: 138 – https://bmcgenomics.biomedcentral.com/articles/10.1186/s12864-019-5522-7 – (On our blog : https://plantstomata.wordpress.com/2019/08/15/the-importance-of-ca-for-c4-photosynthesis-and-its-role-in-stomatal-signaling/ )

Kolla V. A., Raghavendra A. S. (2007) – Nitric oxide is a signaling intermediate during bicarbonate-induced stomatal closure in Pisum sativum – Physiologia Plantarum 130: 91–98 – https://doi.org/10.1111/j.1399-3054.2007.00887.x – https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-3054.2007.00887.x – (On our blog : https://plantstomata.wordpress.com/2018/04/30/no-and-bicarbonate-induced-stomatal-closure/ )

Kolla V. A., Vavasseur A., Raghavendra A. S. (2007) – Hydrogen peroxide production is an early event during bicarbonate induced stomatal closure in abaxial epidermis of Arabidopsis –Planta 225: 1421–1429 – doi: 10.1007/s00425-006-0450-6 – (On our blog : https://plantstomata.wordpress.com/2016/07/06/h2o2-is-an-essential-secondary-messenger-during-bicarbonate-induced-stomatal-closure/)

Kollist H., Jossier M., Laanemets K., Sébastien Thomine S. (2011) Anion channels in plant cells – FEBS Journal 278(22): 4277-4292 – DOI: 10.1111/j.1742-4658.2011.08370.x —  http://onlinelibrary.wiley.com/doi/10.1111/j.1742-4658.2011.08370.x/full – (On our blog : https://plantstomata.wordpress.com/2016/07/06/anion-channel-genes-in-stomata/)

Kollist H., Moldau H., Mortensen L., Rasmussen S. K.,Jørgensen L. B. (2000) – Ozone Flux to Plasmalemma in Barley and Wheat is controlled by Stomata rather than by direct Reaction of Ozone with Cell Wall Ascorbate – Journal of Plant Physiology 156(5-6): 645-651 – DOI10.1016/S0176-1617(00)80226-6 – https://www.infona.pl/resource/bwmeta1.element.elsevier-7a8fdc42-2209-357d-8d42-1cd632dfbf41 – (On our blog : https://plantstomata.wordpress.com/2017/10/10/ozone-flux-to-plasmalemma-is-controlled-by-stomata/)

Kollist T., Moldau H., Rasulov B., Oja V., Rämma H., Hüve K., Jaspers P., Kangasjärvi J., Kollist H. (2007) – A novel device detects a rapid ozone-induced transient stomatal closure in intact Arabidopsis and its absence in abi2 mutant – Physiol Plant. 129: 796–803 – https://doi.org/10.1111/j.1399-3054.2006.00851.xhttps://onlinelibrary.wiley.com/doi/10.1111/j.1399-3054.2006.00851.x – (On our blog : https://plantstomata.wordpress.com/2019/03/18/specifying-complex-molecular-and-genetic-interactions-in-rapid-responses-in-stomatal-guard-cells-in-vivo/ )

Kollist H., Nuhkat M., Roelfsema M. R. G. (2014) – Closing gaps: linking elements that control stomatal movement – New Phytol. 203, 44–62 – doi: 10.1111/nph.12832 – (On our blog : https://plantstomata.wordpress.com/2015/06/21/control-of-stomatal-movement/)

Koman V. B., Lew T. T. S., Wong M. H., Kwak S.-Y., Giraldo J. P., Strano M. S. (2017) – Persistent drought monitoring using a microfluidic-printed electro-mechanical sensor of stomata in planta – Lab on a Chip 23 – DOI: 10.1039/c7lc00930ehttps://pubs.rsc.org/en/content/articlelanding/2017/lc/c7lc00930e/unauth#!divAbstract – (On our blog : https://plantstomata.wordpress.com/2019/08/12/persistent-drought-monitoring-using-a-microfluidic-printed-electro-mechanical-sensor-of-stomata-in-planta/ )

Koman V. B., Park M., Lew T. T. S., Wan S., Yarwood E. S., Gong X., Shikdar T. S., Oliver R. J., Cui J., Gordiichuk P., Sarojam R.,  Strano M. S., (2022) – Emerging investigator series: linking nanoparticle infiltration and stomatal dynamics for plant nanobionics – Environmental Science: Nano – https://pubs.rsc.org/en/content/articlelanding/2022/en/d1en01154e/unauth – (On our blog : https://plantstomata.wordpress.com/2022/03/19/stomata-type-and-open-fraction-determine-the-pressure-drop-and-the-infiltration-efficiency-with-spinach-plants-having-the-most-active-stomata/ )

Konarska A. (2005) – Response of leaves of three plant species to aluminium stress – (Reakcja liści trzech gatunków roślin uprawnych na stres glinowy) – Acta Agrobotanica 58(1): 175-184 –https://doi.org/10.5586/aa.2005.023https://pbsociety.org.pl/journals/index.php/aa/article/view/aa.2005.023/1547 – (On our blog : https://plantstomata.wordpress.com/2022/03/09/increased-stomatal-density-with-increasingal-concentration/ )

Kondamudi R., Swamy K. N., Rao Y. V., Kiran T. V., Suman K., Rao D. S., Rao P. R., Subrahmanyam D., Sarla N., Ramana B. K., Voleti S. R. (2016) – Gas exchange, carbon balance and stomatal traits in wild and cultivated rice (Oryza sativa L.) genotypes – Acta Physiol Plant. 38(16): 1–9 – https://doi.org/10.1007/s11738-016-2173-zhttps://europepmc.org/article/PMC/6103955 – (On our blog : https://plantstomata.wordpress.com/2020/03/10/stomatal-traits-in-wild-and-cultivated-rice/ )

Kondo N., Maruta I. (1987) – Abscisic acid-induced stomatal closure in Vicia faba epidermal strips. Excretion of solutes from guard cells and increase in elastic modulus of guard cell wall – Plant Cell Physiology 28: 355–364 – https://doi.org/10.1093/oxfordjournals.pcp.a077303 –https://academic.oup.com/pcp/article-abstract/28/2/355/1854700?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2019/03/18/aba-may-cause-an-increase-in-the-elastic-modulus-of-the-cell-walls-of-stomatal-guard-cells/ )

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Kondo T., Kajita R., Miyazaki A., Hokoyama M., Nakamura-Miura T., Mizuno S., Masuda Y., Irie K., Tanaka Y., Takada S., Kakimoto T., Sakagami Y. (2010) – Stomatal density is controlled by a mesophyll-derived signaling molecule – Plant Cell Physiol. 51: 1–8 – doi: 10.1093/pcp/pcp180 – Epub 2009 Dec 9 – https://www.ncbi.nlm.nih.gov/pubmed/20007289 – (On our blog : https://plantstomata.wordpress.com/2018/05/03/stomagen-is-a-mesophyll-to-epidermis-signaling-molecule-that-positively-regulates-stomatal-density/ )

Kong D., Hu H.-C., Okuma E., Lee Y., Lee H. S., Munemasa S., Cho D., Ju C., Pedoeim L., Rodriguez B., Wang J., Im W., Murata Y., Pei Z.-M., Kwak J. (2016) – L-Met Activates Arabidopsis GLR Ca2+ Channels Upstream of ROS Production and Regulates Stomatal Movement – Cell Reports 17(10): 2553-2561 – https://doi.org/10.1016/j.celrep.2016.11.015 – https://www.cell.com/cell-reports/fulltext/S2211-1247(16)31556-X?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS221112471631556X%3Fshowall%3Dtrue – (On our blog : https://plantstomata.wordpress.com/2019/02/15/l-met-regulates-stomatal-movement/ )

Kong D., Karve R., Willet A., Chen M. K., Oden J., Shpak E. D. (2012) – Regulation of plasmodesmatal permeability and stomatal patterning by the glycosyltransferase-like protein KOBITO1 –  Plant Physiology 159: 156-168 – https://doi.org/10.1104/pp.112.194563 – http://www.plantphysiol.org/content/159/1/156 – (On our blog : https://plantstomata.wordpress.com/2018/05/03/kobito1-and-stomatal-patterning/ )

Kong W., Yoo M.-J., Noble J. D., Kelley T. M., Li J., Kirst M., Assmann S. M., Chen S. (2019) – Molecular changes in Mesembryanthemum crystallinum guard cells underlying the C3 to CAM transition – biorxivhttp://dx.doi.org/10.1101/607333https://www.biorxiv.org/content/biorxiv/early/2019/04/12/607333.full.pdf – (On our blog : https://plantstomata.wordpress.com/2019/05/03/c3-to-cam-transition-of-ice-plant-stomatal-guard-cells/ )

Konings A. G., Williams A. P., Gentine P., (2017) – Sensitivity of grassland productivity to aridity controlled by stomatal and xylem regulation – Nature Geoscience 10(4): 284-288 – DOI: 10.1038/ngeo2903 – http://www.military-technologies.net/2017/12/07/how-grasslands-regulate-their-productivity-in-response-to-droughts/ – (On our blog : https://plantstomata.wordpress.com/2017/12/09/coordination-between-stomatal-closure-strategies-and-the-loss-of-xylem-conductance-under-drought/)

Kono A.Umeda-Hara C.Adachi S., Nagata N.Konomi M.Nakagawa T.Uchimiya H.Umeda M. (2007) – The Arabidopsis D-Type Cyclin CYCD4 Controls Cell Division in the Stomatal Lineage of the Hypocotyl Epidermis – The Plant Cell 19(4): 1265-1277 –  http://dx.doi.org/10.1105/tpc.106.046763 – http://www.plantcell.org/content/19/4/1265.full – (On our blog : https://plantstomata.wordpress.com/2016/04/02/cyclin-cycd4-controls-cell-division-in-the-stomatal-lineage/)

Konrad K. R. , Hedrich R. (2008) – The use of voltage-sensitive dyes to monitor signal-induced changes in membrane potential-ABA triggered membrane depolarization in guard cells – Plant Journal 55: 161-173 – doi: 10.1111/j.1365-313X.2008.03498.x – https://www.ncbi.nlm.nih.gov/pubmed/18363788 – (On our blog : https://plantstomata.wordpress.com/2018/05/05/voltage-sensitive-dyes-provide-an-excellent-tool-for-the-study-of-changes-in-the-membrane-potential-in-vacuole-as-well-as-guard-cell-populations/ )

Konrad W., Katul G., Roth-Nebelsick A., Grein M. (2017) – A reduced order model to analytically infer atmospheric CO2 concentration from stomatal and climate data – Advances in Water Resources 104: 145–157 – https://doi.org/10.1016/j.advwatres.2017.03.018https://www.sciencedirect.com/science/article/pii/S0309170816305024 – (On our blog : https://plantstomata.wordpress.com/2019/08/13/a-reduced-order-model-to-analytically-infer-atmospheric-co2-concentration-from-stomatal-and-climate-data/ )

Konrad W., Roth-Nebelsick, A., Grein, M. (2008) Modelling of stomatal density response to atmospheric CO2. – Journal of Theoretical Biology 253: 638–658 – https://doi.org/10.1016/j.jtbi.2008.03.032 – https://www.sciencedirect.com/science/article/pii/S0022519308001677 – (On lour blog : https://plantstomata.wordpress.com/2018/05/05/stomatal-density-response-to-atmospheric-co2/

Konstantinos P. A.., Toumi I., Panaglotis M. N., Roubelakis-Angelakis K. A.(2010) – ABA-dependent amine oxidases-derived H2O2 affects stomata conductance – Plant Signal. Behav.5: 1153–1156 – https://doi.org/10.4161/psb.5.9.12679https://www.tandfonline.com/doi/full/10.4161/psb.5.9.12679 – (On our blog : https://plantstomata.wordpress.com/2019/07/08/aba-dependent-amine-oxidases-derived-h2o2-affects-stomata-conductance/ )

Kopka J., Provart N. J., Müller-Röber B. (1997) Potato guard cells respond to drying soil by a complex change in the expression of genes related to carbon metabolism and turgor regulation. – Plant Journal 11: 871882 – DOI: 10.1046/j.1365-313X.1997.11040871.x – (On our blog : https://plantstomata.wordpress.com/2016/07/07/stomatal-gene-expression-under-drought-stress-conditions/ )

Korn R. W. (1972) – Arrangement of stomata on the leaves of Pelargonium zonale and Sedum stahlii – Ann. Bot. 36325–333 – DOI: 10.1093/oxfordjournals.aob.a084592 – https://academic.oup.com/aob/article-abstract/36/2/325/190820?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2018/05/05/arrangement-of-stomata-in-pelargonium-zonale-and-sedum/

Korn R. W. (1993) – Evidence in dicots for stomatal patterning by inhibition. – International Journal of Plant Sciences 154367–377 – https://doi.org/10.1086/297118 – http://www.journals.uchicago.edu/doi/abs/10.1086/297118 – (On our blog : https://plantstomata.wordpress.com/2018/01/20/stomatal-patterning-by-inhibition/ )

Korn R. W. (2009) – A new hypothesis for stomatal placement in Arabidopsis. – J. Theor. Biol. 260: 172–174 – DOI: 10.1016/j.jtbi.2009.05.012 – https://www.ncbi.nlm.nih.gov/pubmed/19481098 – (No abstract available)

Korn R. W., Fredrick G. W. (1973) – Development of D-type stomata in the leaves of Ilex crenata var. convexa – Ann. Bot. Lond. 37: 647-656 – DOI: 10.1093/oxfordjournals.aob.a084731 – https://academic.oup.com/aob/article-abstract/37/3/647/151284?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2018/08/28/development-of-d-type-stomata/ )

Körner C. (1981) – Stomatal behaviour and water potential in apricot (Prunus armeniaca) with symptoms of wilt disease (Chondrostereum) – Angewandte Botanik 55: 469–476 – ISSN : 0066-1759 –

Körner C. (1988) – Does global increase of CO2 alter stomatal density? – Flora 181: 253-257 – https://doi.org/10.1016/S0367-2530(17)33116-X – https://www.sciencedirect.com/science/article/pii/S036725301733116X – (On our blog : https://plantstomata.wordpress.com/2018/05/05/global-increase-of-co2-and-stomatal-density/ )

Körner C. (2017) – When meta-analysis fails: A case about stomata – Global Change Biology 23(7): 2533–2534 – https://doi.org/10.1111/gcb.13700 – https://onlinelibrary.wiley.com/doi/10.1111/gcb.13700 – (On our blog : https://plantstomata.wordpress.com/2020/09/09/when-meta-analysis-fails-a-case-about-stomata/ )

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Launiainen S., Katul G. G., Kolari P., Vesala T., Hari P. (2011) – Empirical and optimal stomatal controls on leaf and ecosystem level CO2 and H2O exchange rates – Agricultural and Forest Meteorology 151: 1672-1689 – https://doi.org/10.1016/j.agrformet.2011.07.001https://researchportal.helsinki.fi/en/publications/empirical-and-optimal-stomatal-controls-on-leaf-and-ecosystem-lev – (On our blog : https://plantstomata.wordpress.com/2022/03/01/linkage-between-the-leaf-level-stomatal-conductance-gs-response-to-environmental-stimuli-and-canopy-level-mass-exchange-processes/ )

Laur J., Hacke U.G. (2013) – Transpirational demand affects aquaporin expression in poplar roots – Journal of Experimental Botany 64(8): – DOI: 10.1093/jxb/ert096 – https://www.researchgate.net/publication/236228367_Transpirational_demand_affects_aquaporin_expression_in_poplar_roots – (On our blog : https://plantstomata.wordpress.com/2018/12/02/stomatal-conductance-and-modulation-of-water-uptake-in-a-dynamic-manner/

Laurin É. , Nunes M.C.N. , Émond J.-P., Brecht J. K. (2006) – Residual effect of low-pressure stress during simulated air transport on Beit Alpha-type cucumbers: Stomata behavior – Postharvest Biology and Technology 41(2): 121-127 – DOI: 10.1016/j.postharvbio.2005.09.012 – https://www.infona.pl/resource/bwmeta1.element.elsevier-865ba4b2-f898-33fc-807d-3924301b6aa1 – (On our blog : https://plantstomata.wordpress.com/2017/10/16/stomata-behavior-during-simulated-air-transport/)

Lavergne A., Voelker S., Gsank A., Graven H., de Boer H. J., Daux V., Robertson I., Dorado-Linan I., Martinez-Sancho E., Battipaglia G., Bloomfield K. J., Still C. J., Meinzer F. C., Dawson T. E., Camarero J. J., Clisby R., Fang Y., Menzel A., Keen R. M., Roden J. S., Prentice I. C. (2019) – Historical changes in the stomatal limitation of photosynthesis: empirical support for an optimality principle – New Phytologist 225(6) – https://doi.org/10.1111/nph.16314https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.16314 – (On our blog : https://plantstomata.wordpress.com/2020/05/04/the-stomatal-limitation-of-photosynthesis/ )

Lavilla M., Seral A., Murciano A., Molino S., Fuente P. de la, Gabriel y Galán J. M. (2017) – Stomatal traits in Iberian populations of Osmunda regalis (Osmundaceae, Polypodiopsida) and its relationship with bioclimatic variables – Acta Botanica Malacitana 42(1): 5-13 – https://doi.org/10.24310/abm.v42i1.3029https://revistas.uma.es/index.php/abm/article/view/3029 – (On our blog : https://plantstomata.wordpress.com/2022/02/17/102118/ )

Lavoie-Lamoureux A., Sacco D., Risse P. A., Lovisolo C. (2017) – Factors influencing stomatal conductance in response to water availability in grapevine: a meta-analysis – Physiologia Plantarum 159: 468–482 – DOI: 10.1111/ppl.12530https://pubmed.ncbi.nlm.nih.gov/27859326/ – (On our blog : https://plantstomata.wordpress.com/2022/05/10/a-continuum-exists-in-the-range-of-stomatal-sensitivities-to-water-stress-in-vitis-vinifera-rather-than-an-isohydric-anisohydric-dichotomy/)

Law S. R. (2021) – Those in glass houses – Physiologia Plantarum (In the spotlight) – https://doi.org/10.1111/ppl.13354https://onlinelibrary.wiley.com/doi/full/10.1111/ppl.13354 – (On our blog : https://plantstomata.wordpress.com/2022/03/29/silica-deposited-in-gurad-cells-increased-their-sensitivity-to-aba/ )

Lawlor D. W. (2002) – Limitation to Photosynthesis in Water‐stressed Leaves: Stomata vs. Metabolism and the Role of ATP – Annals of Botany 89(7): 871–885 – https://doi.org/10.1093/aob/mcf110 – https://academic.oup.com/aob/article/89/7/871/151155/Limitation-to-Photosynthesis-in-Water-stressed – (On our blog : https://plantstomata.wordpress.com/2017/10/26/stomata-vs-metabolism-and-the-role-of-atp/)

Lawlor D. W., Lake J. V. (1976) –  Evaporation rate, leaf water potential and stomatal conductance in Lolium, Trifolium and Lysimachia in drying soil – J. Appl. Ecol. 13: 639–646 – DOI: 10.2307/2401809 – https://www.jstor.org/stable/pdf/2401809.pdf?seq=1#page_scan_tab_contents (On our blog : https://plantstomata.wordpress.com/2018/11/25/evaporation-rate-leaf-water-potential-and-stomatal-conductance-in-drying-soil/

Lawrence S. R., Gaitens M., Guan Q., Dufresne C., Chen S. (2020) – S-Nitroso-Proteome Revealed in Stomatal Guard Cell Response to Flg22 – Int. J. Mol. Sci. 21(5): 1688 – https://doi.org/10.3390/ijms21051688https://www.mdpi.com/1422-0067/21/5/1688 – (On our blog : https://plantstomata.wordpress.com/2020/04/13/the-molecular-mechanisms-and-regulatory-roles-of-sno-in-stomata-immunity-against-bacterial-pathogens/ )

Lawson S. S., Pijut P. M., Michler C.H. (2014) – The cloning and characterization of a poplar stomatal density gene – Genes and Genomics 36: 427–441 – https://doi.org/10.1007/s13258-014-0177-x – https://link.springer.com/article/10.1007/s13258-014-0177-x – (On our blog : https://plantstomata.wordpress.com/2018/05/08/a-poplar-stomatal-density-gene/ )

Lawson S. S., Pijut P. M., Michler C.H. (2014) – Comparison of Arabidopsis Stomatal Density Mutants Indicates Variation in Water Stress Responses and Potential Epistatic Effects – J. Plant Biol. (2014) 57:162-173 –http://www.fs.fed.us/nrs/pubs/jrnl/2014/nrs_2014_lawson_002.pdf – (On our blog : https://plantstomata.wordpress.com/2015/03/27/stomata-and-biomass/)

Lawson S. S., Pijut P. M., Michler C. H. (2014) – Comparison of Arabidopsis stomatal density mutants indicates variation in water stress responses and potential epistatic effects – J. Plant Biol. 57: 162–173 – DOI: 10.1007/s12374-014-0017-1 – https://www.fs.usda.gov/treesearch/pubs/46282 – (On our blog : https://plantstomata.wordpress.com/2018/10/30/comparison-of-stomatal-density-mutants-indicates-variation-in-water-stress-responses/

Lawson T. (2009) – Guard cell photosynthesis and stomatal function – New Phytol. 181: 13-34 – doi: 10.1111/j.1469-8137.2008.02685.x – (On our blog : https://plantstomata.wordpress.com/2016/03/18/7709/)

Lawson T. (2019) – Stomatal-based systems analysis of water use efficiency – UKri – https://gtr.ukri.org/project/BA273D8A-FB5A-45AC-A59F-804214C14D7B – (On our blog : https://plantstomata.wordpress.com/2019/05/04/stomatal-based-systems-analysis-of-wue/ )

Lawson T., Blatt M. R. (2014) – Stomatal size, speed, and responsiveness impact on photosynthesis and water use efficiency – Plant Physiol. 164(4): 1556-1570 – doi: 10.1104/pp.114.237107 – Epub 2014 Feb 27 – https://plantstomata.wordpress.com/2016/07/21/the-rapidity-of-stomatal-responses/)

Lawson T., Blatt R. M. (2014) – Stomatal size, speed, and responsiveness impact on photosynthesis and water use efficiency – Plant Physiol.164: 1556–1570 – https://doi.org/10.1104/pp.114.237107 – http://www.plantphysiol.org/content/164/4/1556 – (On our blog : https://plantstomata.wordpress.com/2018/10/30/stomatal-size-speed-and-responsiveness-impact-on-photosynthesis-and-water-use-efficiency/ )

Lawson T., Craigon J., Black C. R., Colls J. J., Landon G., Weyers J. D. (2002) –  Impact of elevated CO2 and O3 on gas exchange parameters and epidermal characteristics in potato (Solanum tuberosum L.) –  J. Exp. Bot. 53(369): 737–746 – https://doi.org/10.1093/jexbot/53.369.737 – https://academic.oup.com/jxb/article/53/369/737/614573 – (On our blog : https://plantstomata.wordpress.com/2018/05/08/impact-of-elevated-co2-and-o3-on-stomata/ )

Lawson T., Flexas J. (2020) – Fuelling life: recent advances in photosynthesis research – The Plant Journal 101(4): – https://doi.org/10.1111/tpj.14698https://onlinelibrary.wiley.com/doi/10.1111/tpj.14698 – (On our blog : https://plantstomata.wordpress.com/2020/05/11/stomata-and-recent-advances-in-photosynthesis-research/ )

Lawson T., James W., Weyers J. (1998) – A surrogate measure of stomatal aperture – Journal of Experimental Botany 49(325): 1397–1403 – (On our blog : https://plantstomata.wordpress.com/2017/09/19/measuring-stomatal-aperture/)

Lawson T., Lefebvre S., Baker N. R., Morison J. I. L., Raines C. A. (2008) – Reductions in mesophyll and guard cell photosynthesis impact on the control of stomatal responses to light and CO2  – Journal of Experimental Botany 59: 3609–3619 – (On our blog: https://plantstomata.wordpress.com/2016/07/21/photosynthesis-and-stomatal-responses-to-light-and-co2/)

Lawson T., Matthews J. (2020) – Guard Cell Metabolism and Stomatal Function – Annual Review of Plant Biology 71: 273-302 – https://doi.org/10.1146/annurev-arplant-050718-100251https://www.annualreviews.org/doi/abs/10.1146/annurev-arplant-050718-100251 (On our blog : https://plantstomata.wordpress.com/2020/05/12/guard-cell-metabolism-and-stomatal-function/ )

Lawson T., McElwain J. C. (2016) – Evolutionary trade-offs in stomatal spacing – New Phytologist 210: 1149-1151  – DOI: 10.1111/nph.13972 – http://onlinelibrary.wiley.com/doi/10.1111/nph.13972/full – (On our blog : https://plantstomata.wordpress.com/2016/05/10/stomatal-spacing/)

Lawson T., Morison J. I. L. (2010) – Guard Cell Photosynthesis – Plant Physiol. & Developm., 6th ed., Essay 10.1 – http://6e.plantphys.net/essay10.01.html – (On our blog : https://plantstomata.wordpress.com/2015/10/24/guard-cell-photosynthesis-and-fluorescence/)

Lawson T., Oxborough K., Morison J. I. L., Baker N. R. (2002) – Responses of Photosynthetic Electron Transport in Stomatal Guard Cells and Mesophyll Cells in Intact Leaves to Light, CO2, and Humidity – Plant Physiology 128(1): 52-62 – DOI: https://doi.org/10.1104/pp.010317 http://www.plantphysiol.org/content/128/1/52 – (On our blog : https://plantstomata.wordpress.com/2019/05/07/photosynthetic-electron-transport-in-stomatal-guard-cell-chloroplasts-responds-to-internal-not-ambient-co2-concentration/ )

Lawson T., Oxborough K., Morison J. I., Baker N. R. (2003) – The responses of guard and mesophyll cell photosynthesis to CO2, O2, light, and water stress in a range of species are similar – J. Exp. Bot. 54: 1743–1752 – doi: 10.1093/jxb/erg186 – https://www.ncbi.nlm.nih.gov/pubmed/12773521 – (On our blog : https://plantstomata.wordpress.com/2018/05/08/photosynthetic-efficiency-in-stomata-is-determined-by-the-same-factors-that-determine-it-in-the-mesophyll/ )

Lawson T., Oxborough K., Morison J. I., Baker N. R. (200x) – Evaluating guard cell photosynthesis in intact green leaves using chlorophyll fluorescence imaging – http://www.publish.csiro.au/sa/pdf/SA0403560 – (On our blog : https://plantstomata.wordpress.com/2017/11/13/evaluating-photosynthesis-in-stomata-in-intact-green-leaves/)

Lawson T., Simkin A. J., Kelly G., Granot D. (2014) – Mesophyll photosynthesis and guard cell metabolism impacts on stomatal behaviour – New Phytol. 203: 1064–1081 – doi: 10.1111/nph.12945 – https://nph.onlinelibrary.wiley.com/doi/full/10.1111/nph.12945 – (On our blog : https://plantstomata.wordpress.com/2020/01/09/stomatal-guard-cell-metabolism-impacts-on-stomatal-behaviour/ )

Lawson T., Terashima I., Fujita T.,,Wang Y. (2018) – “Coordination between photosynthesis and stomatal behavior,” in The Leaf: A Platform for Performing Photosynthesis. Advances in Photosynthesis and Respiration (Including Bioenergy and Related Processes) 44, eds W. Adams III and I. Terashima (Cham: Springer) – 141–161 – doi: 10.1007/978-3-319-93594-2_6https://link.springer.com/chapter/10.1007%2F978-3-319-93594-2_6 – (On our blog : https://plantstomata.wordpress.com/2022/01/03/the-mechanisms-and-signal-transduction-pathways-that-facilitate-the-well-observed-correlation-between-mesophyll-photosynthetic-rates-and-stomatal-conductance/ )

Lawson T., Vialet-Chabrand S. (2018) – Speedy stomata, photosynthesis and plant water use efficiency – New Phytol. Online Version of Record – https://doi.org/10.1111/nph.15330 – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.15330?af=R – (On our blog : https://plantstomata.wordpress.com/2018/07/12/the-rapidity-of-stomatal-responses-2/ )

Lawson T., von Caemmerer S., Baroli I. (2011) – Photosynthesis and stomatal behaviour – Progress in Botany 72: 265-304 – https://doi.org/10.1007/978-3-642-13145-5_11https://link.springer.com/chapter/10.1007/978-3-642-13145-5_11 – (On our blog : https://plantstomata.wordpress.com/2019/05/07/photosynthesis-and-stomatal-behaviour/ )

Lawson T., Weyers J. D. B., A’Brook R. (1998) – The nature of heterogeneity in the stomatal behaviour of Phaseolus vulgaris L. primary leaves – Journal of Experimental Botany  49(325): 1387–1395 – The_nature_of_heterogeneity_in_the_stoma.pdf – (On our blog : https://plantstomata.wordpress.com/2017/12/14/the-nature-of-heterogeneity-in-the-stomatal-behaviour/)

Laxalt A. M., Garcia Mata C., Lamattina L. (2016) – The dual role of nitric oxide in guard cells: promoting and attenuating the ABA and phospholipid-derived signals leading to the stomatal closure – Frontiers Plant Sci. 7: 476 – doi: 10.3389/fpls.2016.00476 – http://journal.frontiersin.org/article/10.3389/fpls.2016.00476/full – (On our blog : https://plantstomata.wordpress.com/2016/09/03/dual-role-of-no-in-stomata/)

Laza M. R. C., Kondo M., Ideta O., Barlaan E., Imbe T. (2010) – Quantitative trait loci for stomatal density and size in lowland rice – Euphytica 172: 149–158 – DOI: 10.1007/s10681-009-0011-8 – Quantitative_trait_loci_for_stomatal_den.pdf – (On our blog : https://plantstomata.wordpress.com/2017/12/13/quantitative-trait-loci-for-stomatal-density-and-size-in-lowland-rice/)

Le J., Liu X.-G., Yang K.-Y., Chen X.-L., Zou J.-J., Wang H.-Z., Wang M., Vanneste S., Morita M., Tasaka M., Ding Z.-J., Friml J., Beeckman T., Sack F. (2014) – Auxin transport and activity regulate stomatal patterning and development – Nature Communications 5: – doi: 10.1038/ncomms4090 – http://www.nature.com/articles/ncomms4090 – (On our blog : https://plantstomata.wordpress.com/2016/12/16/auxin-stomatal-patterning-and-development/)

Le J., Zou J., Yang K., Wang M. (2014) – Signaling to stomatal initiation and cell division – Front. Plant Sci. 5: Art. 297 – https://doi.org/10.3389/fpls.2014.00297 –  fpls-05-00297.pdf – (On our blog : https://plantstomata.wordpress.com/2018/12/13/signaling-involved-in-stomatal-initiation-and-in-divisions-in-the-cell-lineage/ )

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Leakey A. D. B. (2019) – PE1200: Phenomics of Stomata and Water Use Efficiency in C4 Species – Plant & Animal Genome Conference XXVII, San Diego – https://pag.confex.com/pag/xxvii/meetingapp.cgi/Paper/37365 – (On our blog : https://plantstomata.wordpress.com/2019/03/21/phenomics-of-stomata/ )

Leakey A., Bernacchi C., Ort D., Long S. (2006) – Long-term growth of soybean at elevated [CO2] does not cause acclimation of stomatal conductance under fully open-air conditions – Plant Cell Environ. 29: 1794–1800 – https://doi.org/10.1111/j.1365-3040.2006.01556.x – https://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-3040.2006.01556.x – (On our blog : https://plantstomata.wordpress.com/2018/05/11/elevated-co2-and-stomatal-conductance/ )

Lebaudy A.Pascaud F.Véry A. A., Alcon C.Dreyer I.Thibaud J. B.Lacombe B. (2010) – Preferential KAT1-KAT2 heteromerization determines inward K+ current properties in Arabidopsis guard cells – J Biol Chem 285: 62656274 – DOI: 10.1074/jbc.M109.068445 – http://www.jbc.org/content/285/9/6265/F1.expansion.html –  https://www.ncbi.nlm.nih.gov/pubmed/20040603 – (On our blog : https://plantstomata.wordpress.com/2018/05/11/arabidopsis-guard-cell-inward-shaker-channels-are-mainly-heteromers-of-kat1-and-kat2-subunits/ )

Lebaudy A., Vavasseur A., Hosy E., Dreyer I., Leonhardt N., Thibaud J.-B., Véry A.-A., Simonneau T., Sentenac H. (2008) – Plant adaptation to fluctuating environment and biomass production are strongly dependent on guard cell potassium channels – Proc. Natl Acad. Sci. USA 105:5271–5276 – doi: 10.1073/pnas.0709732105 – (On our blog : https://plantstomata.wordpress.com/2016/07/22/gckin-activity-plays-pleiotropic-roles-in-stomata/)

Lebourgeois F., Lévy G., Aussenac G., Clerc B., Willm F. (1998) – Influence of soil drying on leaf water potential, photosynthesis, stomatal conductance and growth in two black pine varieties – Ann. For. Sci. 55: 287-299 – DOI: 10.1051/forest:19980302https://www.afs-journal.org/articles/forest/abs/1998/03/AFS_0003-4312_1998_55_3_ART0002/AFS_0003-4312_1998_55_3_ART0002.html – (On our blog : https://plantstomata.wordpress.com/2021/04/02/the-influence-of-long-term-soil-water-deficit-on-growth-and-physiological-processes-stomatal-conductance/ )

LeBrasseur N. (2006) – Stomata fight infection – J Cell Biol 174(7): 909b – https://doi.org/10.1083/jcb.1747rr1https://rupress.org/jcb/article/174/7/909b/44546/Stomata-fight-infection – (On our blog : https://plantstomata.wordpress.com/2020/12/29/stomata-fight-infection/ )

Lechowski Z. (1997) – Stomatal response to exogenous cytokinin treatment of the hemiparasite Melampyrum arvense L. before and after attachment to the host – Biol. Plant. 39: 13- 21 – https://doi.org/10.1023/A:1000392502943 – https://link.springer.com/article/10.1023%2FA%3A1000392502943#citeas – (On our blog : https://plantstomata.wordpress.com/2018/05/11/stomatal-response-to-exogenous-cytokinin-treatment/ )

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Lee D. M., Assmann S. M. (1992) – Stomatal responses to light in the facultative Crassulacean acid metabolism species, Portulacaria afra – Physiol. Plant. 85: 35–42 – https://doi.org/10.1111/j.1399-3054.1992.tb05260.x – https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-3054.1992.tb05260.x – (On our blog : https://plantstomata.wordpress.com/2018/10/30/portulacaria-afra-individuals-performing-c3-metabolism-possess-typical-stomatal-responses-to-light/ )

Lee E., Liu X., Eglit Y., Sack F. (2013)  – FOUR LIPS and MYB88 conditionally restrict the G1/S transition during stomatal formation – J. Exp. Bot. 64(16): 5207-5219 – doi: 10.1093/jxb/ert313 – http://jxb.oxfordjournals.org/content/64/16/5207.abstract?ijkey=22e89154124e32cc948637e8891ecf4c6450bd72&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2016/09/27/four-lips-flp-and-myb88-genes-and-nonstomatal-epidermal-cells/)

Lee E., Lucas J. R., Goodrich J., Sack F. D. (2014) – Arabidopsis Guard Cell Integrity Involves the Epigenetic Stabilization of the FLP and FAMA Transcription Factor Genes – THE PLANT JOURNAL 78(4) – DOI: 10.1111/tpj.12516 – https://www.researchgate.net/publication/261030727_Arabidopsis_Guard_Cell_Integrity_Involves_the_Epigenetic_Stabilization_of_the_FLP_and_FAMA_Transcription_Factor_Genes – (On our blog : https://plantstomata.wordpress.com/2015/06/21/stomata-guard-cell-integrity/)

Lee E., Lucas J. R., Sack F. D. (2014)  – Deep functional redundancy between FAMA and FOUR LIPS in stomatal development – Plant Journ. 78(4): 555-565 – doi: 10.1111/tpj.12489 – Epub 2014 Apr 23 – http://www.ncbi.nlm.nih.gov/pubmed/24571519 – (On our blog : https://plantstomata.wordpress.com/2016/07/23/interactions-between-flp-and-fama-with-the-retinoblastoma-related-rbr-protein-in-stomatal-functions/)

Lee E. H., Beedlow P. A., Brooks J. R., Tingey D. T., Wickham C., Rugh W. (2021) – Physiological responses of Douglas-fir to climate and forest disturbances as detected by cellulosic carbon and oxygen isotope ratios – Tree Physiology, tpab122 – https://doi.org/10.1093/treephys/tpab122, https://academic.oup.com/treephys/advance-article/doi/10.1093/treephys/tpab122/6370950 – (On our blog : https://plantstomata.wordpress.com/2021/10/30/94924/ )

Lee H. C. (2002) – Sensing, Signaling and Cell Adaptation – Cell and Molecular Response to Stress – https://www.sciencedirect.com/topics/immunology-and microbiology/plant-stoma – (On our blog : https://plantstomata.wordpress.com/2021/03/02/3-cadpr-and-plant-response-to-environmental-stress/ )

Lee H. J., Tucker E. B., Crain R. C., Lee Y. (1993) – Stomatal Opening Is Induced in Epidermal Peels of Commelina communis L. by GTP Analogs or Pertussis Toxin – Plant Physiol. 102(1): 95-100 – doi: 10.1104/pp.102.1.95https://pubmed.ncbi.nlm.nih.gov/12231800/ – (On our blog : https://plantstomata.wordpress.com/2021/10/02/93996/ )

Lee H. K., Khaine I., Kwak M.-J., Jang J., Lee T., Lee J. K., Kim L. R., Kim W. I., Oh K. S., Woo S.-Y. (2017) – The relationship between SO2 exposure and plant physiology: A mini review – Horticulture, Environment and Biotechnology 58(6): 523-529 – DOI: 10.1007/s13580-017-0053-0https://www.researchgate.net/publication/321800325_The_relationship_between_SO2_exposure_and_plant_physiology_A_mini_review – (On our blog : https://plantstomata.wordpress.com/2021/09/27/stomata-so2-exposure-and-plant-physiology/ )

Lee J. H., Jung J. H., Park C. M. (2017) – Light inhibits COP1-Mediated degradation of ICE transcription factors to induce stomatal development in Arabidopsis – The Plant Cell 29: 2817–2830 – https://doi.org/10.1105/tpc.17.00371https://pubmed.ncbi.nlm.nih.gov/29070509/ – (On our blog : https://plantstomata.wordpress.com/2021/07/09/light-is-directly-linked-with-the-ice-directed-signaling-module-via-the-cop1-mediated-protein-surveillance-system-in-the-modulation-of-stomatal-development/ )

Lee J. S. (1998) – The mechanism of stomatal closing by salicylic acid in Commelina communis L. – Plant Biol. (1998) 41: 97 – https://doi.org/10.1007/BF03030395 – https://link.springer.com/article/10.1007/BF03030395#citeas – (On our blog : https://plantstomata.wordpress.com/2018/01/07/stomatal-closing-by-sa/ )

Lee J. S. (2000) – The Effects of Two Abscisic Acid Analogues, WL19224 and WL19377, on Stomatal Closure – Journal of Plant Biology 43(1): 56-59 –doi:10.1007/BF03031037https://link.springer.com/article/10.1007/BF03031037 – (On our blog : https://plantstomata.wordpress.com/2021/05/09/the-effect-on-stomatal-closure-by-aba-and-its-analogues-wl19224-and-wl19377/ )

Lee J. S. (2005) – Three Possible Mechanisms for Stomatal Opening in Response to Light – The Korean Journal of Ecology 28(2): 105-112 – https://doi.org/10.5141/jefb.2005.28.2.105 http://koreascience.or.kr/article/JAKO200509905763269.page – (On our blog : https://plantstomata.wordpress.com/2021/08/08/three-possible-mechanisms-for-the-light-response-of-stomata/ )

Lee J. S. (2006) – The Relationship between Stomatal Opening and Photosynthetic Activity of the Mesophyll in Commelina communis L. – Korean Journal of Environmental Science 15(12): 1109-1117 –

Lee J. S. (2010) – Stomatal Opening Mechanism of CAM Plants –  J. Plant Biol. (2010) 53: 19-23 –  https://doi.org/10.1007/s12374-010-9097-8 – https://link.springer.com/article/10.1007/s12374-010-9097-8 – (On our blog : https://plantstomata.wordpress.com/2017/09/26/stomata-of-cam-plants/)

Lee J. S. (2013) – Do really close stomata by soil drying ABA produced in the roots and transported in transpiration stream? – American J Plant Science 4: 169-173 – https://doi.org/10.4236/ajps.2013.41022https://www.scirp.org/journal/paperinformation.aspx?paperid=27662 – (On our blog : https://plantstomata.wordpress.com/2021/05/09/stomatal-response-to-the-abrupt-water-stress-is-very-rapid/ )

Lee J. S. (2014) – The Electrophysiology Application on Guard Cells to See the Influence of Carbon Dioxide – Journal of Environmental Science International (한국환경과학회지) 23(5): 763-770 – https://doi.org/10.5322/JESI.2014.5.763https://www.koreascience.or.kr/article/JAKO201416760765129.pa1ff8ge – (On our blog : https://plantstomata.wordpress.com/2021/05/08/co2-flowing-could-stimulate-proton-efflux-which-is-a-necessary-precursor-of-stomatal-opening/ )

Lee J. S. (2020) – What kinds of osmotic materials induce stomatal opening – https://d197for5662m48.cloudfront.net/documents/publicationstatus/47940/preprint_pdf/d0644cd3c9095dee41a82050fae97f49.pdf – (On our blog : https://plantstomata.wordpress.com/2022/01/07/although-various-solutes-including-k-are-required-for-stomata-to-open-sucrose-is-believed-to-be-the-most-important-substance-that-can-increase-the-vacuoles-osmotic-pressure/ )

Lee J. S., Bowling D. J. F. (1992) – Effect of the mesophyll on stomatal opening in Commelina communis – Journal of Experimental Botany 43: 951–957 – https://doi.org/10.1093/jxb/43.7.951 – https://academic.oup.com/jxb/article-abstract/43/7/951/531126?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2018/10/27/the-mesophyll-plays-an-important-role-in-stomatal-opening-in-the-light/ )

Lee J. S., Bowling D. J. F. (1992) – Effect of the mesophyll on stomatal opening in Commelina communis – J. Exp. Bot. 43: 951–957 – doi: 10.1093/jxb/43.7.951 – http://www.esalq.usp.br/lepse/imgs/conteudo_thumb/Effect-of-the-Mesophyll-on-Stomatal-Opening-in-Commelina-communis.pdf  – (On our blog : https://plantstomata.wordpress.com/2016/02/16/the-effect-of-a-number-of-factors-on-the-opening-of-stomata/)

Lee J. S., Bowling D. J. F. (1993) – Influence of the Mesophyll on the Change of Electrical Potential Difference of Guard Cells Induced by Red Light and CO2 in Commelina communis L. and Tradescantia virginiana L. – Korean Journal of Plant Biology 36(4): 383-389 –

Lee J. S., Bowling D. J. F. (1993) – The effect of a mesophyll factor on the swelling of guard cell protoplasts of Commelina communis – Journal of Plant Physiology 142: 203–207 – https://doi.org/10.1016/S0176-1617(11)80964-8 –https://www.sciencedirect.com/science/article/pii/S0176161711809648?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/04/08/the-effect-of-a-mesophyll-factor-on-the-swelling-of-stomatal-guard-cell-protoplasts/ )

Lee J. S., Bowling D. J. F. (1995) – Influence of the mesophyll on stomatal opening – Aust. J Plant Physiol. 22: 357-363 – https://doi.org/10.1071/PP9950357https://www.publish.csiro.au/fp/PP9950357 – (On our blog : https://plantstomata.wordpress.com/2021/05/09/the-participation-of-the-mesophyll-in-stomatal-control/ )

Lee J. S., Hnilova M., Maes M., Lin Y.-C. L., Putarjunan A., Han S.-K., Avila J.,Torii K. U. (2015) – Competitive binding of antagonistic peptides fine-tunes stomatal patterning – Nature 522: 439–443 – doi:10.1038/nature14561 – (On our blog : https://plantstomata.wordpress.com/2016/07/04/antagonistic-peptides-and-stomatal-patterning/)

Lee J. -S., Kim B.-W. (1997) – Stomatal response by ozone – Korean J. Ecol. 20(2): 83-94 – http://koreascience.or.kr/article/JAKO199711919962498.pdf – (On our blog : https://plantstomata.wordpress.com/2021/09/04/stomatal-closing-by-ozone/ )

Lee J. S., Kuroha T., Hnilova M., Khatayevich D., Kanaoka M. M., McAbee J. M., Sarikaya M., Tamerler C., Torii K. U. (2012) – Direct interaction of ligand-receptor pairs specifying stomatal patterning  Genes Dev. 26: 126-136 – doi: 10.1101/gad.179895.111 – (On our blog : https://plantstomata.wordpress.com/2016/02/16/ligand-receptor-pairs-specifying-stomatal-patterning/)

Lee J. S., Webb A. A. R. (1997) – The effect ethylene on stomatal closing in Commelina communis L.

Lee L. R., Bergmann D. C. (2019) – The plant stomatal lineage at a glance – Journal of Cell Science 132: jcs228551 – doi: 10.1242/jcs.228551https://jcs.biologists.org/content/132/8/jcs228551.abstract – (On our blog : https://plantstomata.wordpress.com/2019/08/13/the-stomatal-lineage-is-dynamic-and-flexible-altering-stomatal-production-in-response-to-environmental-change/ )

Lee L. R., Wengier D. L., Bergmann D. C. (2019) – Cell-type–specific transcriptome and histone modification dynamics during cellular reprogramming in the Arabidopsis stomatal lineage – PNAS 116(43): 21914-21924 – https://doi.org/10.1073/pnas.1911400116https://www.pnas.org/content/116/43/21914 – (On our blog : https://plantstomata.wordpress.com/2020/08/27/transcriptome-and-histone-modification-dynamics-in-the-arabidopsis-stomatal-lineage/ )

Lee M., Choi Y., Burla B., Kim Y.-Y., Jeon B., Maeshima M., Yoo J.-Y., Martinoia M., Lee Y. (2008) – The ABC transporter AtABCB14 is a malate importer and modulates stomatal response to CO2 – Nature Cell Biol. 10: 1217–1223 – (On our blog : https://plantstomata.wordpress.com/2016/07/23/atabcb14-modulates-stomatal-movement/)

Lee R. (1967) – The hydrologic importance of transpiration control by stomata – Water Res. AGU100 3(3): 737-752 – https://doi.org/10.1029/WR003i003p00737https://agupubs.onlinelibrary.wiley.com/doi/abs/10.1029/WR003i003p00737 – (On our blog : https://plantstomata.wordpress.com/2019/11/27/the-hydrologic-importance-of-transpiration-control-by-stomata/ )

Lee R., Gates D. M. (1964) – Diffusion resistance in leaves as related to their stomatal anatomy and microstructure – Am. J. Botany 31: 963-975 –

Lee S., Choi H., Suh S., Doo I. S., Oh K. Y., Choi E. J., et al. (1999) – Oligogalacturonic acid and chitosan reduce stomatal aperture by inducing the evolution of reactive oxygen species from guard cells of tomato and Commelina communis – Plant Physiol. 121: 147–152 – doi: 10.1104/pp.121.1.147 – http://www.plantphysiol.org/content/121/1/147 – (On our blog : https://plantstomata.wordpress.com/2018/05/11/guard-cells-infected-by-pathogens-may-close-their-stomata-via-a-pathway-involving-h2o2-production/ )

Lee S., Ishiga Y., Clermont K., Mysore K. S. (2013) – Coronatine inhibits stomatal closure and delays hypersensitive response cell death induced by nonhost bacterial pathogens – Peer J. 1, e34 – doi:  10.7717/peerj.34 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3628748/ – (On our blog : https://plantstomata.wordpress.com/2018/05/11/stomatal-closure-induced-by-a-nonhost-pathogen-was-disrupted-by-cor/ )

Lee S., Rojas C. M., Oh S., Kang M., Choudhury S. R., Lee H.-K., Allen R. D., Pandey S., Mysore K. S. (2018) – Nucleolar GTP-Binding Protein 1-2 (NOG1-2) Interacts with Jasmonate-ZIMDomain Protein 9 (JAZ9) to Regulate Stomatal Aperture during Plant Immunity – Int. J. Mol. Sci. 19: 1922 – doi:10.3390/ijms19071922file:///C:/Users/wille/Downloads/ijms-19-01922.pdf – (On our blog : https://plantstomata.wordpress.com/2022/03/02/the-function-of-a-small-gtpase-nog1-2-in-guard-cell-signaling-and-early-plant-defense-in-response-to-bacterial-pathogen/ )

Lee S., Senthil-Kumar M., Kang M., Rojas C. M., Tang Y., Oh S., Choudhury S. R., Lee H.-K., Ishiga Y., Allen R. D., Pandey S., Mysore K. S. (2017) – The small GTPase, nucleolar GTP-binding protein 1 (NOG1), has a novel role in plant innate immunity – Scientific Reports 7: Nr.: 9260 – doi:10.1038/s41598-017-08932-9 – https://www.nature.com/articles/s41598-017-08932-9 – (On our blog : https://plantstomata.wordpress.com/2017/09/17/the-new-functional-role-of-small-gtpase-nog1-in-guard-cell-signaling-for-stomatal-response/)

Lee S. C.Lan W.Buchanan B. B.Luan S. (2009) – A protein kinase-phosphatase pair interacts with an ion channel to regulate ABA signaling in plant guard cells – Proc Natl Acad Sci USA 106: 21419–21424 – doi: 10.1073/pnas.0910601106 – (On our blog : https://plantstomata.wordpress.com/2016/07/24/aba-signaling-is-mediated-by-a-physical-interaction-chain-to-regulate-stomatal-movements/)

Lee S. C., Lim C. W., Lan W., He K., Luan S. (2013) – ABA Signaling in guard cells entails a dynamic protein–protein interaction relay from the PYL-RCAR Family receptors to ion channels- Mol. Plant 6: 528–538 – doi: 10.1093/mp/sss078 – (On our blog : https://plantstomata.wordpress.com/2016/07/25/aba-and-a-dynamic-protein-protein-interaction-relay-from-the-pyl-rcar-family-receptors-to-ion-channels/)

Lee S. C., Luan S. (2012) ABA signal transduction at the crossroad of biotic and abiotic stress responses – Plant, Cell & Environment 35(1): 53 – DOI: 10.1111/j.1365-3040.2011.02426.x – http://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.2011.02426.x/full – (On our blog : https://plantstomata.wordpress.com/2016/07/25/aba-signal-transduction-and-activation-of-ion-channels-in-guard-cells-and-stomatal-closure/ )

Lee S. H., Tewari R. K., Hahn E. J., Paek K. Y. (2007) – Photon flux density and light quality induce changes in growth, stomatal development, photosyntesis plantlets – Plant Cell Tiss. Org. Cult. 90: 141-151 – doi:10.1007/s11240-006-9191-2 – http://link.springer.com/article/10.1007/s11240-006-9191-2 – (On our blog : https://plantstomata.wordpress.com/2016/12/19/quality-and-quantity-of-light-affect-stomatal-development/)

Lee T. T. (1965) – Sugar content and stomatal width as related to ozone injury in tobacco leaves – Canadian Journal of Botany 43(6): 677-685 – https://doi.org/10.1139/b65-075https://www.nrcresearchpress.com/doi/abs/10.1139/b65-075 – (On our blog : https://plantstomata.wordpress.com/2020/05/23/high-levels-of-sucrose-and-reducing-sugars-were-associated-with-closure-of-stomata/ )

Lee Y., Assmann S. M. (1990)Diacylglycerol induces both ion pumping in patch clamped guard cell protoplasts and stomatal opening – Plant Physiology 93(1 Suppl.): 17 – https://eurekamag.com/research/030/899/030899253.php

Lee Y., Assmann S. M. (1991) – Diacylglycerols induce both ion pumping in patch-clamped guard-cell protoplasts and opening of intact stomata – Proc Natl Acad Sci USA. 88(6): 2127–2131 – PMID: 11607161 PMCID: PMC51182 – https://www.ncbi.nlm.nih.gov/pubmed/11607161 – (On our blog : https://plantstomata.wordpress.com/2018/05/12/diacylglycerols-and-opening-of-intact-stomata/

Lee Y., Choi Y. B., Suh S., Lee J., Assmann S. M., Joe C. O., Kelleher J. F., Crain R. C. (1996)Abscisic acid-induced phosphoinositide turnover in guard cell protoplasts of Vicia faba – Plant Physiol. 110: 987–996 – http://dx.doi.org/10.1104/pp.110.3.987 – (On our blog : https://plantstomata.wordpress.com/2016/07/26/phosphoinositide-signaling-and-coupling-aba-to-guard-cell-shrinking-and-stomatal-closure/)

Lee Y., Kim Y. J., Kim M.-H., Kwak J. M. (2016) – MAPK Cascades in Guard Cell Signal Transduction – Front. Plant Sci. 7:80 – http://dx.doi.org/10.3389/fpls.2016.00080 – (On our blog  : https://plantstomata.wordpress.com/2016/02/29/mapk-mediated-guard-cell-signaling-in-stomata/)

Lee Y., Kim Y.-W., Jeon B. W., Park K.-Y., Suh S. J., Seo J., Kwak J. M., Martinoia E., Hwang I., Lee Y. (2007) – Phosphatidylinositol 4,5-bisphosphate is important for stomatal opening – Plant J. 52: 803–816 – PMID:17883374 – DOI:10.1111/j.1365-313X.2007.03277.x – (On our blog : https://plantstomata.wordpress.com/2016/07/26/full-stomatal-opening-and-ptdins45p2/)

Lee Y., Lee H. J., Crain R. C., Lee A., Korn S. J. (1994) – Polyunsaturated fatty acids modulates stomatal aperture and two distinct K+ channel currents in guard cells – Cell. Signal. 6: 181–186 – doi: 10.1016/0898-6568(94)90075-2 – https://www.ncbi.nlm.nih.gov/pubmed/8086281 – (On our blog : https://plantstomata.wordpress.com/2018/05/12/fatty-acids-regulate-stomatal-aperture-by-modulation-of-two-different-k-channels/

Lefoulon C., Boxall S. F., Hartwell J., Blatt M. R. (2020) – Crassulacean acid metabolism guard cell anion channel activity follows transcript abundance and is suppressed by apoplastic malate – New Phytol. 227(6): 1847-1857 – doi: 10.1111/nph.16640 – Epub 2020 Jun 16 – PMID: 32367511 – https://pubmed.ncbi.nlm.nih.gov/32367511/ – (On our blog : https://plantstomata.wordpress.com/2022/01/03/the-diurnal-cycle-of-anion-channel-gene-transcription-rather-than-the-physiological-signal-of-mal-release-is-a-key-factor-in-the-inverted-cam-stomatal-cycle/ )

Lehmann P., Or D. (2015) – Effects of stomata clustering on leaf gas exchange. – New Phytol. 207: 1015–1025 – doi:10.1111/nph.13442 – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.13442 – (On our blog : https://plantstomata.wordpress.com/2018/05/12/effects-of-stomata-clustering-on-leaf-gas-exchange/ )

Lei Z. Y., Han J. M., Yi, X. P., Zhang W. F., Zhang Y. L. (2018) – Coordinated variation between veins and stomata in cotton and its relationship with water-use efficiency under drought stress – Photosynthetica  56: 1326-1335 –  https://doi.org/10.1007/s11099-018-0847-z – https://link.springer.com/article/10.1007/s11099-018-0847-z – (On our blog : https://plantstomata.wordpress.com/2018/09/24/coordinated-changes-in-vein-and-stomatal-density-improve-the-wue-of-cotton-under-drought-stress/ )

Leick E. (1927) – Untersuchungen über den Einfluß des Lichtes auf die öffnungsweite unterseitiger und oberseitiger Stomata desselben Blattes – Jahrbücher für Wissenschaftliche Botanik 67: 771848 –

Leick E. (1955) Periodische Neuanlage von Blattstomata – Flora 14245–64 – 

Leidi E. O., Lopez J. M., Lopez M., Gutierrez J. C. (1993) – Searching for tolerance to water stress in cotton genotypes: photosynthesis, stomatal
conductance and transpiration – Photosynthetica 28: 383-390 –

Leila (2015) – How do stomata help conserve water? – Socratic, Biology Topics – https://socratic.org/questions/how-do-stomata-help-conserve-water – (On our blog : https://plantstomata.wordpress.com/2019/01/14/74774/ )

Leinonen I., Grant O. M., Tagliavia C. P. P., Chaves M. M., Jones H. G. (2006) – Estimating stomatal conductance with thermal imagery – Plant, Cell and Environment 29: 1508–1518 – doi: 10.1111/j.1365-3040.2006.01528.xEstimating_stomatal_conductance_with_the.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/19/estimating-stomatal-conductance-with-thermal-imagery/ )

Leitgeb H. (1888) – Beiträge zur Physiologie der Spaltöffnungsapparate – Mitt. Bot. Inst. Graz, Jena 1: 123-

Lekhak H. D., Sen D. N. (1982) – Stomatal responses towards neutral red uptake and particulate movement in some arid zone plants – Biologia Plantarum (Praha) 24(2): 101-108 – (On our blog : https://plantstomata.wordpress.com/2017/03/28/37084/)

Lemichez E., Wu Y., Sanchez J.  P., Mettouchi A., Mathur J., Chua N. H. (2001) – Inactivation of AtRac1 by abscisic acid is essential for stomatal closure – Genes Dev.15: 1808–1816 – doi:10.1101/gad.900401 – (On our blog : https://plantstomata.wordpress.com/2016/07/27/atrac1-is-a-central-element-for-plant-adaptation-to-drought-by-stomatal-closure/)

Lemtiri-Chlieh F. (1996) – Effects of internal K+ and ABA on the voltage- and time-dependence of the outward K+-rectifier in Vicia guard cells – J Membr Biol 1563: 105–116 – https://doi.org/10.1007/s002329900114 – https://link.springer.com/article/10.1007%2Fs002329900114 – (On our blog : https://plantstomata.wordpress.com/2018/05/14/k-aba-and-stomata/

Lemtiri-Chlieh F., MacRobbie E. A. C. (1994) –  Role of calcium in the modulation of Vicia guard cell potassium channels by abscisic acid: a patch clamp study – J. Membr. Biol. 137: 99107 – DOI: 10.1007/BF00233479 – (On our blog : https://plantstomata.wordpress.com/2016/07/27/ca2-k-and-aba-in-stomatal-closure/)

Lemtiri-Chlieh F., MacRobbie E. A. C., Brearley C. A. (2000) – Inositol hexakisphosphate is a physiological signal regulating the K+ -inward rectifying conductance in guard cells – Proc. nat. Acad. Sci. USA 97: 8687-8692 – DOI: 10.1073/pnas.140217497https://www.ncbi.nlm.nih.gov/pubmed/10890897?dopt=Abstract – (On our blog : https://plantstomata.wordpress.com/2019/05/27/insp6-may-play-a-major-role-in-the-physiological-response-of-stomatal-guard-cells-to-aba/ )

Lemtiri-Chlieh F., MacRobbie E. A. C., Webb A. A. R., Manison N. F., Brownlee C., Skepper J. N.,Chen J., Prestwich G. D., Brearley C. A. (2003) – Inositol hexakisphosphate mobilizes an endomembrane store of calcium in guard cells – Proc. Natl. Acad. Sci. U.S.A. 100: 10091 – doi: 10.1073/pnas.1133289100 – (On our blog : https://plantstomata.wordpress.com/2016/07/27/insp6-as-an-endomembrane-acting-calcium-release-signal-in-stomata/)

Leng Q., Huang L., Hua B., Lou C. (1998) – Grey relation function between local electrical potential and stomatal behavior during light exposure in plants – Chinese Science Bulletin 43(19): 1642-1646 – https://doi.org/10.1007/BF02883410https://link.springer.com/article/10.1007/BF02883410 – (On our blog : https://plantstomata.wordpress.com/2019/03/30/lep-could-represent-the-dominant-factor-in-executing-the-stomatal-movement-under-the-light-exposure/ )

Leon J. (2021) – Deceleration of cell cycle underpins a switch from proliferative-to-terminal division in plant stomatal lineage (bioRxiv) – Plantae – https://plantae.org/deceleration-of-cell-cycle-underpins-a-switch-from-proliferative-to-terminal-division-in-plant-stomatal-lineage-biorxiv/ – (On our blog : https://plantstomata.wordpress.com/2021/07/22/particular-combinations-of-cell-cycle-regulators-deployed-at-highly-specific-developmental-stages-carry-out-crucial-roles-in-plant-stomatal-lineage/ )

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Li J., Zhang G.-Z., Li X., Wang Y., Wang F.-Z., Li X.-M. (2019) – Seasonal change in response of stomatal conductance to vapor pressure deficit and three phytohormones in three tree species – Plant Signaling & Behavior 14(12) – https://doi.org/10.1080/15592324.2019.1682341https://www.tandfonline.com/doi/full/10.1080/15592324.2019.1682341 – (On our blog : https://plantstomata.wordpress.com/2020/01/13/seasonal-change-in-response-of-stomatal-conductance-to-vapor-pressure-deficit-and-three-phytohormones/ )

Li J.-H., Liu Y.-Q., Lü P., Lin H.-F., Bai Y., Wang X.-C. et al. (2009) – A signaling pathway linking nitric oxide production to heterotrimeric G protein and hydrogen peroxide regulates extra cellular calmodulin induction of stomatal closure in Arabidopsis – Plant Physiol. 150: 114–124 – doi: 10.1104/pp.109. 137067 – http://www.plantphysiol.org/content/150/1/114 – (On our blog : https://plantstomata.wordpress.com/2018/05/15/a-signaling-pathway-leading-to-extcam-induced-stomatal-closure/ )

Li K., Huang J., Song W., Wang J., Lv S., Wang X. (2019) – Automatic segmentation and measurement methods of living stomata of plants based on the CV model – Plant Methods 15: 67 https://doi.org/10.1186/s13007-019-0453-5https://link.springer.com/article/10.1186/s13007-019-0453-5#citeas – (On our blog : https://plantstomata.wordpress.com/2019/08/14/measurement-methods-of-living-stomata/ )

Li L.‐J., Ren F., Gao X.‐Q., Wei P.‐C., Wang X.‐C. (2013) – The reorganization of actin filaments is required for vacuolar fusion of guard cells during stomatal opening in Arabidopsis – Plant, Cell & Environment 36: 484– 497 – https://doi.org/10.1111/j.1365-3040.2012.02592.xhttps://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.2012.02592.x – (On our blog : https://wordpress.com/block-editor/post/plantstomata.wordpress.com/81325 )

Li M., Wang C., Song J., Chi Y., Wang X., Wu Y. (2008) – Evolutional trends of leaf stomatal and photosynthetic characteristics in wheat evolutions – Acta Ecologica Sinica 28(11): 5385-5391 – https://doi.org/10.1016/S1872-2032(09)60010-Xhttps://www.sciencedirect.com/science/article/abs/pii/S187220320960010X – (On our blog : https://plantstomata.wordpress.com/2020/04/15/as-ploidy-increased-the-stomatal-length-width-perimeter-and-area-were-found-to-increase/ )

Li N., Dong F., Liu T., Yang J., Shi Y., Wang S., Sun D. Jing R. (2022) – Quantitative trait loci mapping and candidate gene analysis of stoma-related traits in wheat (Triticum aestivum L.) glumes – Peer J. 10: e13262 – https://doi.org/10.7717/peerj.13262https://peerj.com/articles/13262/ – (On our blog : https://plantstomata.wordpress.com/2022/05/19/106685/ )

Li Q., Hou J., He N., Xu L., Zhang Z. (2021) – Changes in leaf stomatal traits of different aged temperate forest stands – J. For. Res. 32: 927–936 – https://doi.org/10.1007/s11676-020-01135-5https://link.springer.com/article/10.1007/s11676-020-01135-5#citeas – (On our blog : https://plantstomata.wordpress.com/2022/05/15/spatial-variation-in-stomatal-traits-across-forest-patches-does-not-need-to-be-incorporated-in-future-ecological-models/ )

Li Q., Serbin S. P., Lamour J., Davidson K., Ely K., Rogers A. (2022) – Implementation and evaluation of the unified stomatal optimization approach in the Functionally Assembled Terrestrial Ecosystem Simulator (FATES) – EGU Geoscientific Model Development – DOI: 10.5194/gmd-2021-414https://www.researchgate.net/publication/358104303_Implementation_and_evaluation_of_the_unified_stomatal_optimization_approach_in_the_Functionally_Assembled_Terrestrial_Ecosystem_Simulator_FATES – (On our blog : https://plantstomata.wordpress.com/2022/05/14/the-25-parameterization-of-stomatal-conductance-models-and-current-model-response-to-drought-are-the-critical-areas-for-improving-model-simulation-of-co2-and-water-fluxes-in-tropical-forests/ )

Li Q., Wang Y.-J., Liu C.-K., Pei Z.-M., Shi W.-L. (2017) – The crosstalk between ABA, nitric oxide, hydrogen peroxide, and calcium in stomatal closing of Arabidopsis thaliana – Published Online: 2017-10-31 – https://doi.org/10.1515/biolog-2017-0126 – https://www.degruyter.com/view/j/biolog.2017.72.issue-10/biolog-2017-0126/biolog-2017-0126.xml?utm_source=TrendMD&utm_medium=cpc&utm_campaign=Biologia_TrendMD_0 – (On our blog : https://plantstomata.wordpress.com/2018/01/19/aba-nitric-oxide-hydrogen-peroxide-and-calcium-in-stomatal-closing/ )

Li Q., Yu L.-j., Deng Y., Li W., Li M.-t., Cao J.-h. (2007) – Leaf epidermal characters of Lonicera japonica and Lonicera confuse and their ecology adaptation – J. For. Res. 18: 103-108  – https://link.springer.com/article/10.1007%2Fs11676-007-0020-1 – (On our blog : https://plantstomata.wordpress.com/2017/03/02/stomata-in-lonicera-dicots-2/)

Li R. T., Zhang Y. N., Tian D. L. (2004) – Studies on Stomata of Citrus Plant Leaves – J. Fru. Sci. 21(5): 419–424 –

Li S., Assmann S. M., Albert R. (2006) –  Predicting essential components of signal transduction networks: a dynamic model of guard cell abscisic acid signaling – PLoS Biol.4:e312 – doi: 10.1371/journal.pbio.0040312 – (On our blog : https://plantstomata.wordpress.com/2016/07/29/a-dynamic-model-of-guard-cell-abscisic-acid-signaling/)

Li S., Harley P. C., Niinemets Ü. (2017) – Ozone-induced foliar damage and release of stress volatiles is highly dependent on stomatal openness and priming by low-level ozone exposure in Phaseolus vulgaris – Plant, Cell & Environment – doi: 10.1111/pce.13003 – http://onlinelibrary.wiley.com/doi/10.1111/pce.13003/abstract – (On our blog : https://plantstomata.wordpress.com/2017/06/19/key-role-of-stomatal-conductance-in-controlling-ozone-uptake-leaf-injury-and-volatile-release/)

Li S., Li L., Fan W., Ma S., Zhang C., Kim J. C., Wang K., Russinova E., Zhu Y., Zhou Y. (2022) – LeafNet: a tool for segmenting and quantifying stomata and pavement cells – The Plant Cell 34(4): 1171–1188 –  https://doi.org/10.1093/plcell/koac021https://academic.oup.com/plcell/article-abstract/34/4/1171/6515637?redirectedFrom=fulltext&login=false – (On our blog : https://plantstomata.wordpress.com/2022/04/22/leafnet-a-tool-that-automatically-localizes-stomata-segments-pavement-cells-and-reports-multiple-morphological-parameters-for-a-variety-of-leaf-epidermal-images/ )

Li S., Li X., Wei Z., Liu F. (2020) – ABA-mediated modulation of elevated CO2 on stomatal response to drought – Current Opinion in Plant Biology – Available online 11 January 2020 – https://doi.org/10.1016/j.pbi.2019.12.002https://www.sciencedirect.com/science/article/pii/S1369526619301177 – (On our blog : https://plantstomata.wordpress.com/2020/01/24/aba-mediated-modulation-of-elevated-co2-on-stomatal-response-to-drought/ )

Li S., Liu J., Liu H., Qiu R., Gao Y., Duan A. (2021) – Role of Hydraulic Signal and ABA in Decrease of Leaf Stomatal and Mesophyll Conductance in Soil Drought-Stressed Tomato – Front Plant Sci. 12: 653186 – doi: 10.3389/fpls.2021.653186 – Erratum in: Front Plant Sci. 12: 710792 – PMID: 33995449 – PMCID: PMC8118518 – https://pubmed.ncbi.nlm.nih.gov/33995449/ – (On our blog : https://plantstomata.wordpress.com/2021/11/26/leaf-stomatal-conductance-gs-shows-a-higher-sensitivity-to-drought-than-mesophyll-conductance-gm/ )

Li S., Zhang J., Liu L., Wang Z., Li Y., Guo L., Li Y., Zhang X., Ren S., Zhao B., Zhang N., Guo Y.-D. (2020) SlTLFP8 reduces water loss to improve water-use efficiency by modulating cell size and stomatal density via endoreduplication – Plant, Cell & Environmente 43(11): 2666-2679 – https://doi.org/10.1111/pce.13867https://onlinelibrary.wiley.com/doi/10.1111/pce.13867 – (On our blog : https://plantstomata.wordpress.com/2022/04/14/sltlfp8-a-member-of-tlp-family-regulates-water-deficient-resistance-by-modulating-water-loss-via-affecting-stomatal-density/ )

Li T., Kromdijk J., Heuvelink E., van Noort F. R., Kaiser E., Marcelis L. F. M. (2016) – Effects of Diffuse Light on Radiation Use Efficiency of Two Anthurium Cultivars Depend on the Response of Stomatal Conductance to Dynamic Light Intensity – Front. Plant Sci., 04 February 2016 | http://dx.doi.org/10.3389/fpls.2016.00056 – http://journal.frontiersin.org/article/10.3389/fpls.2016.00056/full – (On our blog : https://plantstomata.wordpress.com/2016/03/28/response-of-stomatal-conductance-to-dynamic-light-intensity/)

Li X., Li J. H., He S., Pang Z., Lin S., Li H. (2020) – Investigation of Stomata in Cut ‘Master’ Carnations: Organographic Distribution, Morphology, and Contribution to Water Loss – HortScience 55(7): 1144-1147 – https://doi.org/10.21273/HORTSCI14945-20https://journals.ashs.org/hortsci/view/journals/hortsci/55/7/article-p1144.xml – (On our blog : https://plantstomata.wordpress.com/2020/11/15/the-differential-contributions-of-stomata-in-leaves-stems-and-floral-organs-to-water-loss-2/ )

Li X., Li J. H., Wang W., Chen N.Z., Ma T. S., Xi Y. N., Zhang X. L., Lin H. F., Bai Y., Huang S. J., Chen Y. L. (2014) – ARP2/3 complex-mediated actin dynamics is required for hydrogen peroxide-induced stomatal closure in Arabidopsis – Plant Cell Environ 37: 1548- 1560 – https://doi.org/10.1111/pce.12259 –https://onlinelibrary.wiley.com/doi/full/10.1111/pce.12259 – (On our blog : https://plantstomata.wordpress.com/2019/05/07/a-possible-causal-relation-between-the-production-of-h2o2-and-actin-dynamics-in-aba%e2%80%90mediated-stomatal-guard-cell-signalling/ )

Li X., Ma X., He J. (2013) – Stomatal Bioassay in Arabidopsis Leaves – Bio-protocol 3(19): e921 – DOI: 10.21769/BioProtoc.921https://bio-protocol.org/e921 – (On our blog : https://plantstomata.wordpress.com/2020/11/12/how-to-measure-stomatal-apertures-under-multiple-treatments/ )

Li X., Palta J. A., Liu F. (2022) – Editorial: Modulation of Stomatal Response by Elevated CO2 in Plants Under Drought and Heat Stress – Frontiers in Plant Science 13: 843999 – https://doi.org/10.3389/fpls.2022.843999https://www.frontiersin.org/articles/10.3389/fpls.2022.843999/full – (On our blog : https://plantstomata.wordpress.com/2022/04/25/modulation-of-stomatal-response-by-elevated-co2/ )

Li X., Smith R., Choat B., Tissue D. T. (2020) – Drought resistance of cotton (Gossypium hirsutum) is promoted by early stomatal closure and leaf shedding – Funcional Plant Biology 47(2): 91-98 – https://www.publish.csiro.au/fp – (On our blog: https://plantstomata.wordpress.com/2020/01/24/irrigation-should-be-applied-shortly-following-stomatal-closure-to-ensure-canopy-photosynthesis-during-and-after-water-deficit/ )

Li X., Wilkinson S., Shen J., Forde B. G., Davies W. J. (2017) – Stomatal and growth responses to hydraulic and chemical changes induced by progressive soil drying – J Exp Bot 68(21-22): 5883-5894 – doi: 10.1093/jxb/erx381https://pubmed.ncbi.nlm.nih.gov/29126265/ – (On our blog : https://plantstomata.wordpress.com/2020/07/15/stomatal-and-growth-responses-to-hydraulic-and-chemical-changes/ )

Li X., Wu T., Cheng Y., Tan N.-D., Jiang F., Liu S.-Z., Chu G.-W., Meng Z., Liu J.-X. (2020) – Ecophysiological adaptability of four tree species in the southern subtropical evergreen broad-leaved forest to warming – Chin J Plant Ecol. 44(12): 1203-1214 – DOI: 10.17521/cjpe.2020.0318https://www.plant-ecology.com/EN/10.17521/cjpe.2020.0318 – (On our blog : https://plantstomata.wordpress.com/2022/04/18/leaf-stomatal-traits-anatomical-structure-and-photosynthetic-characteristics-were-measured-to-represent-the-abilities-of-stomatal-regulation-leaf-tissue-regulation-and-nutrient-maintenance-respecti/ )

Li Y., Ding Y., Qu L., Li X., Lai Q., Zhao P., Gao Y., Xiang C., Cang C., Liu X., Sun L. (2022) –  Structure of the Arabidopsis guard cell anion channel SLAC1 suggests activation mechanism by phosphorylation – Nat Commun 13: 2511 – https://doi.org/10.1038/s41467-022-30253-3https://www.nature.com/articles/s41467-022-30253-3#citeas – (On our blog : https://plantstomata.wordpress.com/2022/05/20/understanding-of-the-regulation-of-slac1-activity-and-stomatal-aperture-in-plants/ )

Li Y., Li H., Li Y., Zhang S. (2017) – Improving water-use efficiency by decreasing stomatal conductance and transpiration rate to maintain higher ear photosynthetic rate in drought-resistant wheat – The Crop Journal 5: 231–239 – https://doi.org/10.1016/j.cj.2017.01.001https://www.sciencedirect.com/science/article/pii/S2214514117300016?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/12/04/drought-resistance-is-regulated-by-stomatal-characteristics-through-a-decrease-in-transpiration-rate-in-order-to-improve-integral-wue-and-photosynthetic-performance-and-through-sustaining-a-higher-ea/ )

Li Y., Wang Y., Wang B., Wang Y., Yu W. (2019) – The Response of Plant Photosynthesis and Stomatal Conductance to Fine Particulate Matter (PM2.5) based on Leaf Factors Analyzing – J. Plant Biol. 62: 120-128 – https://doi.org/10.1007/s12374-018-0254-9https://link.springer.com/article/10.1007/s12374-018-0254-9#citeas – (On our blog : https://plantstomata.wordpress.com/2019/12/07/response-of-plant-photosynthesis-and-stomatal-conductance-to-fine-particulate-matter-pm2-5/ )

Li Y., Xu S., Gao J., Pan S., Wang G. (2016) – Glucose– and mannose-induced stomatal closure is mediated by ROS production, Ca and water channels in Vicia faba – Physiol. Plant. 156(3): 252-261 – doi: 10.1111/ppl.12353 – Epub 2015 Jun 25 – https://www.ncbi.nlm.nih.gov/pubmed/26046775 – (On our blog : https://plantstomata.wordpress.com/2018/05/15/ros-production-is-involved-in-glucose-and-mannose-induced-stomatal-closure/ )

Li Y., Xu S., Gao J., Pan S., Wang G. (2016) – Bacillus subtilis-regulation of stomatal movement and instantaneous water use efficiency in Vicia faba – Plant Growth Regulation 78(1): 43-55 – http://link.springer.com/article/10.1007%2Fs10725-015-0073-7 – (On our blog : https://plantstomata.wordpress.com/2016/04/04/microbes-and-stomatal-movement/)

Li Y., Xu S., Wang Z., He L., Xu K. Wang G. (2018) – Glucose triggers stomatal closure mediated by basal signaling through HXK1 and PYR/RCAR receptors in Arabidopsis – Journ. Exp. Bot. 69(7): 1471-1484 – https://doi.org/10.1093/jxb/ery024 https://academic.oup.com/jxb/article/69/7/1471/4850518 – (On our blog : https://plantstomata.wordpress.com/2019/03/21/glucose-triggered-stomatal-closure-may-be-dependent-on-basal-signaling-through-pyr-rcar-receptors-and-hexokinase1-hxk1/ )

Li Y.-M., Liu J. Z., Shi Y., Zhang F. (2011) Effects of Aluminum Stress on the Stomatal Characteristics and Photosynthesis of Scutellaria baicalensis Georgi Seedlings – Journal of Anhui Agricultural Sciences 2011-10 http://en.cnki.com.cn/Article_en/CJFDTOTAL-AHNY201110051.htm – (On our blog : https://plantstomata.wordpress.com/2016/02/16/effects-of-aluminum-stress-on-the-stomatal-characteristics/)

Li Y. P., Li H. B., Li Y. Y., Zhang S. Q. (2017) –  Improving water-use efficiency by decreasing stomatal conductance and transpiration rate to maintain higher ear photosynthetic rate in drought-resistant wheat – The Crop Journal 5: 231-239 –

Li Y.-Z., Zhao Z.-Q., Song D.-D., Yuan Y.-X., Sun H.-J., Zhao J.-F., Chen Y.-L., Zhang C.-G. (2021) – SnRK2.6 interacts with phytochrome B and plays a negative role in red light-induced stomatal opening – Taylor-Francis Online – https://doi.org/10.1080/15592324.2021.1913307https://www.tandfonline.com/doi/full/10.1080/15592324.2021.1913307?src=recsys – (On our blog : https://plantstomata.wordpress.com/2021/07/28/the-negative-role-of-snrk2-6-in-red-light-induced-stomatal-opening/)

Li Z., Liu D. (2012) – ROPGEF1 and ROPGEF4 are functional regulators of ROP11 GTPase in ABA-mediated stomatal closure in Arabidopsis – FEBS Lett 586(9): 1253-1258 – https://doi.org/10.1016/j.febslet.2012.03.040 – https://www.sciencedirect.com/science/article/pii/S0014579312002402 – (On our blog : https://plantstomata.wordpress.com/2018/05/19/the-role-of-ropgef1-and-ropgef4-in-aba-mediated-stomatal-closure/ )

Li Z., Kang J., Sui N., Liu, D. (2012) – ROP11 GTPase is a negative regulator of multiple ABA responses in Arabidopsis. – J Integr Plant Biol 54(3): 169-179 – doi: 10.1111/j.1744-7909.2012.01100.x – https://www.ncbi.nlm.nih.gov/pubmed/22233300 – (On our blog : https://plantstomata.wordpress.com/2018/05/19/rop11-is-a-negative-regulator-of-multiple-aba-responses/ )

Li Z. H., Liu J. P., Gu H. L., et al. (2016) – Review on the effects of drought stress on plant stomatal characteristics – Subtropical Plant Science 45(2): 195-200 – doi: 10.3969/j.issn.1009-7791.2016.02.021

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Liang K. M. , Lin Z. F. , Ren H. , Liu N. , Zhang Q. M. , Wang J. , Wang Z. F. , Guan L. L. (2010) – Characteristics of sun- and shade-adapted populations of an endangered plant Primulina tabacum Hance – Photosynthetica 48(4): 494-506 – DOI: 10.1007/s11099-010-0066-8  – https://www.infona.pl/resource/bwmeta1.element.springer-c6c9025f-1427-3c2e-b4f7-be821acadc26 – (On our blog : https://plantstomata.wordpress.com/2017/10/20/stomata-in-sun-and-shade-adapted-populations-of-primulina-tabacum-gesneriaceae/)

Liang S.Lu K.Wu Z.Jiang S.-C.Yu Y.-T.Bi C.Xin Q.Wang X.-F.Zhang D.-P. (2015) – A link between magnesium-chelatase H subunit and sucrose nonfermenting 1 (SNF1)-related protein kinase SnRK2.6/OST1 in Arabidopsis guard cell signalling in response to abscisic acid – J. Exp. Bot. 66(20): 6355-6369 – doi: 10.1093/jxb/erv341 – http://jxb.oxfordjournals.org/content/66/20/6355.full – (On our blog : https://plantstomata.wordpress.com/2015/09/30/a-link-between-abarchlh-and-snrk2-6ost1-in-guard-cell-signalling-in-response-to-aba/)

Liang Y.-K., Dubos C., Dodd I. C., Holroyd G. H., Hetherington A. M., Campbell M. M. (2005) – AtMYB61, an R2R3-MYB Transcription Factor Controlling Stomatal Aperture in Arabidopsis thaliana – Current Biology 15(13): 1201-1206 – DOI: 10.1016/j.cub.2005.06.041  – https://www.infona.pl/resource/bwmeta1.element.elsevier-fa396381-caec-31cf-8b44-00de1da5f223 – (On our blog : https://plantstomata.wordpress.com/2017/10/24/atmyb61-encodes-the-first-transcription-factor-implicated-in-the-closure-of-stomata/)

Liang Y.-K., Xie X., Lindsay S. E., Wang Y. B., Masle J., Williamson L., Leyser O., Hetherington A. M. (xxxx) – Cell wall composition contributes to the control of transpiration efficiency in Arabidopsis thaliana – The Plant Journal 64(4): 679 – 686 – DOI: 10.1111/j.1365-313X.2010.04362.x – https://www.infona.pl/resource/bwmeta1.element.wiley-tpj-v-64-i-4-tpj4362 – (On our blog : https://plantstomata.wordpress.com/2017/10/25/genes-involved-in-cell-wall-biosynthesis-will-have-an-impact-on-water-use-efficiency-reduced-stomatal-pore-widths/)

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Liu C., Hölttä T., Tian X., Berninger F., Mäkelä A. (2020) – Weaker Light Response, Lower Stomatal Conductance and Structural Changes in Old Boreal Conifers Implied by a Bayesian Hierarchical Model – Front Plant Sci. 11: 579319 – doi: 10.3389/fpls.2020.579319 – eCollection 2020 – https://pubmed.ncbi.nlm.nih.gov/33240299/ – (On our blog : https://plantstomata.wordpress.com/2021/09/01/the-optimal-state-of-stomatal-behaviour-and-a-bayesian-hierarchical-model/ )

Liu C., Li Y., Xu L., Chen Z., He N. (2019) – Variation in leaf morphological, stomatal, and anatomical traits and their relationships in temperate and subtropical forests – Sci Rep. 9: 5803 doi: 10.1038/s41598-019-42335-2https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6456615/ – (On our blog : https://plantstomata.wordpress.com/2019/07/20/leaf-morphological-stomatal-and-anatomical-traits-in-temperate-and-subtropical-forests/ )

Liu C., Li Y., Xu L., Li M., Wang J., Yan P., He N. (2021) – Stomatal Arrangement Pattern: A New Direction to Explore Plant Adaptation and Evolution – Frontiers in Plant Science 12: 655255 – DOI: 10.3389/fpls.2021.655255https://www.researchgate.net/publication/351231518_Stomatal_Arrangement_Pattern_A_New_Direction_to_Explore_Plant_Adaptation_and_Evolution – (On our blog : https://plantstomata.wordpress.com/2021/05/07/three-indices-to-address-the-shortcoming-of-stomatal-density/ )

Liu C., Muir C. D., Li Y., Xu L., Li M., Zhang J., de Boer H. J., Sack L., Han X.-G., Yu G., He N. (2021) – Scaling between stomatal size and density in forest plants – bioRxiv – doi: https://doi.org/10.1101/2021.04.25.441252https://www.biorxiv.org/content/10.1101/2021.04.25.441252v1 – (On our blog : https://plantstomata.wordpress.com/2021/05/07/understanding-of-optimal-stomatal-conductance-photosynthesis-and-plant-water-use-efficiency/ )

Liu C., Sack L., Li Y., He N. (2021) – Stomatal trait distributions (Contrasting adaptation and optimization of stomatal traits across communities at continental-scale) – bioRxiv preprint – https://doi.org/10.1101/2021.11.30.470674https://www.biorxiv.org/content/10.1101/2021.11.30.470674v1.full.pdf – (On our blog : https://plantstomata.wordpress.com/2022/02/20/102427/ )

Liu F., Andersen M. N., Jacobsen S. E., Jensen C. R. (2005) – Stomatal control and water use efficiency of soybean (Glycine max L. Merr.) during progressive soil drying – Environmental and Experimental Botany 54: 33–40 – https://doi.org/10.1016/j.envexpbot.2004.05.002https://www.sciencedirect.com/science/article/abs/pii/S0098847204000772?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2020/06/01/stomatal-control-and-water-use-efficiency/ )

Liu F., Jensen C. R., Andersen M. N. (2003) – Hydraulic and chemical signals in the control of leaf expansion and stomatal conductance in soybean exposed to drought stress – Functional Plant Biology  30: 65-73 – https://doi.org/10.1071/FP02170http://www.publish.csiro.au/fp/FP02170 – (On our blog : https://plantstomata.wordpress.com/2019/02/04/hydraulic-and-chemical-signals-in-the-control-of-leaf-expansion-and-stomatal-conductance/ )

Liu F.Jensen C. R.Shahanzari A.Andersen M. N.Jacobsen S. E. (2005) – ABA regulated stomatal control and photosynthetic water use efficiency of potato (Solanum tuberosum L.) during progressive soil drying – Plant Science 168: 831836 – http://dx.doi.org/10.1016/j.plantsci.2004.10.016 http://www.sciencedirect.com/science/article/pii/S0168945204004674 – (On our blog : https://plantstomata.wordpress.com/2016/10/02/aba-regulated-stomatal-control-during-progressive-soil-drying/)

Liu F.Shahanzari A.,  Jacobsen S. E., Jensen C. R.,  Janowiak F., Walligorski P., Andersen M. N. (2008) – Effects of Deficit Irrigation and Partial Root-Zone Drying on Soil and Plant Water Status, Stomatal Conductance, Plant Growth and Water Use Efficiency in Tomato during Early Fruiting Stage – Acta horticulturae 792: 413-420 – DOI 10.17660/ActaHortic.2008.792.48 – https://www.researchgate.net/publication/260172503_Effects_of_Deficit_Irrigation_and_Partial_Root-Zone_Drying_on_Soil_and_Plant_Water_Status_Stomatal_Conductance_Plant_Growth_and_Water_Use_Efficiency_in_Tomato_during_Early_Fruiting_Stage – (On our blog : plantstomata.wordpress.com/2017/12/13/effects-of-deficit-irrigation-and-partial-root-zone-drying-on-stomatal-conductance/)

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Liu H., Shen J., Yuan C., Lu D., Acharya B. R., Wang M., Chen D., Zhang W. (2021) – The Cyclophilin ROC3 Regulates ABA-Induced Stomatal Closure and the Drought Stress Response of Arabidopsis thaliana – Front. Plant Sci., 25 May 2021 – https://doi.org/10.3389/fpls.2021.668792https://www.frontiersin.org/articles/10.3389/fpls.2021.668792/full – (On our blog : https://plantstomata.wordpress.com/2022/03/20/roc3-positively-regulates-aba-induced-stomatal-closure/ )

Liu H., Xue S. (2021) – Interplay between hydrogen sulfide and other signaling molecules in the regulation of guard cell signaling and abiotic/biotic stress response – Plant Communications 2(3): 100179 – https://doi.org/10.1016/j.xplc.2021.100179https://www.sciencedirect.com/science/article/pii/S2590346221000572 – (On our blog : https://plantstomata.wordpress.com/2021/07/09/the-regulatory-role-of-h2s-in-stomatal-movement-including-the-dynamic-regulation-of-phytohormones-ion-homeostasis-and-cell-structural-components/ )

Liu J., Elmore J. M., Fuglsang A. T., Palmgren M. G., Staskawicz B. J., Coaker G. (2009) – RIN4 functions with plasma membrane H+-ATPases to regulate stomatal apertures during pathogen attack – PLoS Biol. 7: 1000139 – doi: 10.1371/journal.pbio.1000139 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2694982/ – (On our blog : https://plantstomata.wordpress.com/2018/05/22/rin4-functions-with-the-pm-h-atpases-to-regulate-stomatal-apertures/

Liu J., Hou L., Liu G., Liu X., Wang X. (2011) – Hydrogen sulfide induced by nitric oxide mediates ethylene-induced stomatal closure of Arabidopsis thaliana – Chin. Sci. Bull. 56: 3547–3553 – doi: 10.1007/s11434-011-4819-y – https://link.springer.com/content/pdf/10.1007/s11434-011-4819-y.pdf – (On our blog : https://plantstomata.wordpress.com/2018/05/23/h2s-and-no-are-involved-in-the-signal-transduction-pathway-of-ethylene-induced-stomatal-closure/ )

Liu J., Liu G.-H., Hou L.-X., Liu X. (2010) – Ethylene-induced nitric oxide production and stomatal closure in Arabidopsis thaliana depending on changes in cytosolic pH – Chin. Sci. Bull. 55: 2403–2409 – doi: 10.1007/s11434-010-4033-3 – https://link.springer.com/article/10.1007%2Fs11434-010-4033-3 – (On our blog : https://plantstomata.wordpress.com/2018/04/18/no-production-and-stomatal-closure-depending-on-changes-in-cytosolic-ph/ )

Liu J., Hou Z., Liu G., Hou L., Liu X. (2012) – Hydrogen sulfide may function downstream of nitric oxide in ethylene-induced stomatal closure in Vicia faba L. – J. Integr. Agric. 11: 1644–1653 – doi: 10.1016/S2095-3119(12)60167-1 – https://www.sciencedirect.com/science/article/pii/S2095311912601671 – (On our blog : https://plantstomata.wordpress.com/2018/05/23/h2s-may-represent-a-novel-component-downstream-of-no-in-the-ethylene-induced-stomatal-movement/ )

Liu J., Xia Z., Wang M., Zhang X., Yang T., Wu J. (2013) – Overexpression of a maize E3 ubiquitin ligase gene enhances drought tolerance through regulating stomatal aperture and antioxidant system in transgenic tobacco – Plant Physiol. Biochem. 73: 114–120 –

Liu J.Zhang C.Wei C.Liu X.Wang M.Yu F.Xie Q.Tu J. (2016) – The RING Finger Ubiquitin E3 Ligase OsHTAS Enhances Heat Tolerance by Promoting H2O2-Induced Stomatal Closure in Rice – Plant Physiology 170(1): –  https://doi.org/10.1104/pp.15.00879 – http://www.plantphysiol.org/content/170/1/429 – (On our blog : https://plantstomata.wordpress.com/2017/11/06/ring-finger-ubiquitin-e3-ligase-oshtas-enhances-heat-tolerance-through-modulation-of-hydrogen-peroxide-induced-stomatal-closure/)

Liu J., Zhang F., Zhou J., Chen F., Wang B., Xie X. (2012) – Phytochrome b control of total leaf area and stomatal density affects drought tolerance in rice – Plant Mol. Biol. 78: 289–300 – doi: 10.1007/s11103-011-9860-3https://pubmed.ncbi.nlm.nih.gov/22138855/ – (On our blog : https://plantstomata.wordpress.com/2021/11/19/reduced-stomatal-density-resulted-in-reduced-transpiration-per-unit-leaf-area-in-the-phyb-mutants/ )

Liu K.Fu H.Bei Q.Luan S. (2000) – Inward potassium channel in guard cells as a target for polyamine regulation of stomatal movements – Plant Physiol 124: 13151326 – https://doi.org/10.1104/pp.124.3.1315 – http://www.plantphysiol.org/content/124/3/1315.short – (On our blog : https://plantstomata.wordpress.com/2017/10/03/polyamine-regulation-of-stomatal-movements/)

Liu K., Luan S. (1998) Voltage-dependent K+ channels as targets of osmosensing in guard cells – Plant Cell 10: 19571970 – http://dx.doi.org/10.1105/tpc.10.11.1957 – (On our blog : https://plantstomata.wordpress.com/2016/07/29/k-channels-as-targets-of-osmosensing-in-stomata/)

Liu L., McDonald A. J. S., Stadenberg I., Davies W. J. (2001) – Abscisic acid in leaves and roots of willow: significance for stomatal conductance – Tree Physiol. 21: 759-764 – PMID:11470662 – https://www.ncbi.nlm.nih.gov/pubmed/11470662 – (On our blog : https://plantstomata.wordpress.com/2016/10/02/significance-of-aba-for-stomatal-conductance/)

Liu L., McDonald A. J. S., Stadenberg I., Davies W. J. (2001) – Stomatal and leaf growth responses to partial drying of root tips in willow – Tree Physiol 21(11): 765-770 – doi: 10.1093/treephys/21.11.765https://pubmed.ncbi.nlm.nih.gov/11470663/ – (On our blog : https://plantstomata.wordpress.com/2020/07/15/stomatal-and-leaf-growth-responses-to-partial-drying-of-root-tips/ )

Liu L., Kon H., Matsuoka N. Kobayashi T. (2005) – Coordination between stomatal conductance and leaf-specific hydraulic conductance in maize (Zea mays L. ) – J. Agric. Meteorol. 61(3): 143-152 – https://www.jstage.jst.go.jp/article/agrmet/61/3/61_3_143/_pdf – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/71487 )

Liu L.-M., Qi H., Luo X.-L., Zhang X. – Coordination effect between vapor water loss through plant stomata and liquid water supply in soil-plant-atmosphere continuum (SPAC): a review – Review Ying Yong Sheng Tai Xue Bao. 2008;19(9): 2067-2073 – https://pubmed.ncbi.nlm.nih.gov/19102325/ – (On our blog : https://plantstomata.wordpress.com/2020/07/15/vapor-water-loss-through-plant-stomata-and-liquid-water-supply-in-spac-article-in-chinese/

Liu P., Sun F., Gao R., Dong H. (2012) – RAP2.6L overexpression delays waterlogging induced premature senescence by increasing stomatal closure more than antioxidant enzyme activity – Plant Mol. Biol. 79: 609–622 – doi: 10.1007/s11103-012-9936-8 – https://www.ncbi.nlm.nih.gov/pubmed/22661072 – (On our blog : https://plantstomata.wordpress.com/2018/05/23/rap2-6l-overexpression-delays-waterlogging-induced-premature-senescence-by-increasing-stomatal-closure/ )

Liu S., Jia F., Jiao Z., Wang J., Xia X., Yin W. (2019) – Ectopic expression of secretory peptide PdEPF3 in Arabidopsis confers drought tolerance with reduced stomatal density – Acta Soc Bot Pol. 88(2): 3627 – https://doi.org/10.5586/asbp.3627https://pbsociety.org.pl/journals/index.php/asbp/article/view/asbp.3627/7715 – (On our blog : https://plantstomata.wordpress.com/2022/01/19/reduced-stomatal-density-of-transgenic-plants-and-pdepf3-can-be-used-in-transgenic-breeding-to-enhance-plant-drought-tolerance/ )

Liu S., Li H., Lv X., Ahammed G. J., Xia X., Zhou J., Shi K,, Asami T., Yu J., Zhou Y. (2016) – Grafting cucumber onto luffa improves drought tolerance by increasing ABA biosynthesis and sensitivity – Scientific Reports 6, Article number: 20212 – doi:10.1038/srep20212 – http://www.nature.com/articles/srep20212 – (On our blog : https://plantstomata.wordpress.com/2016/03/24/drought-tolerance-aba-and-stomata/

Liu S.-p., Liu J., Cao J., Bai C., Shi R. (2006) – Stomatal distribution and character analysis of leaf epidermis of jujube under drought stress – Journal of Anhui Agricultural Science 34: 1315–1318 – http://en.cnki.com.cn/Article_en/CJFDTOTAL-AHNY200607018.htm – (On our blog : https://plantstomata.wordpress.com/2018/10/31/stomatal-distribution-in-jujube-under-drought-stress/ )

Liu S., Yang M., Zhao H., Li H., Suo B., Wang Y. (2015) – Exogenous abscisic acid inhibits the water-loss of postharvest romaine lettuce during storage by inducing stomatal closure – Food Sci. Technol, Campinas 35(4): 729-733 – http://dx.doi.org/10.1590/1678-457X.0002https://www.scielo.br/pdf/cta/v35n4/0101-2061-cta-35-4-729.pdf – (On our blog : https://plantstomata.wordpress.com/2020/11/12/aba-can-obviously-reduce-the-transpiration-rate-of-lettuce-leaves-by-promoting-the-stomatal-closure-of-postharvest-lettuce/ )

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Liu T. D., Zhang X. W., Xu Y. (2019) – Influence of red light on the expression of genes on stomatal formation in maize seedlings – Canadian Journal of Plant Science • 7 November 2019 • https://doi.org/10.1139/cjps-2019-0140https://cdnsciencepub.com/doi/10.1139/cjps-2019-0140 – (On our blog : https://plantstomata.wordpress.com/2022/05/02/influence-of-red-light-on-the-expression-of-genes-on-stomatal-formation/ )

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Liu X., Afrin T., Pajerowska-Muhtar K. M. (2019) – Arabidopsis GCN2 kinase contributes to ABA homeostasis and stomatal immunity – Communications Biology  2, Article number: 302  – https://www.nature.com/articles/s42003-019-0544-x – (On our blog : https://plantstomata.wordpress.com/2019/08/13/a-conserved-role-of-gcn2-in-various-forms-of-immune-responses-and-stomatal-immunity/ )

Liu X., Liu H., Gleason S. M., Goldstein G., Zhu S., He P., Hou H., Li R., Ye Q. (2019) – Water transport from stem to stomata: the coordination of hydraulic and gas exchange traits across 33 subtropical woody species – Tree Physiol 39(10): 1665-1674 – doi: 10.1093/treephys/tpz076https://pubmed.ncbi.nlm.nih.gov/31314105/ – (On our blog : https://plantstomata.wordpress.com/2021/03/29/water-transport-efficiencies-of-stem-and-leaf-xylem-are-important-determinants-of-stomatal-conductance/ )

Liu X., Fan Y., Mak M., Babla M., Holford P., Wang F., Chen G. Scott G., Wang G., Shabala S., Zhou M., Chen Z.-H. (2017) – QTLs for stomatal and photosynthetic traits related to salinity tolerance in barley – BMC Genomics 18: 9 – DOI: 10.1186/s12864-016-3380-0https://bmcgenomics.biomedcentral.com/track/pdf/10.1186/s12864-016-3380-0.pdf – (On our blog : https://plantstomata.wordpress.com/2021/12/24/the-lack-of-major-qtls-for-gas-exchange-and-stomatal-traits-under-control-and-saline-conditions-indicates-a-complex-relationship-between-salinity-and-leaf-gas-exchange-under-the-control-of-multiple-ge/ )

Liu X., Mak M., Babla M., Holford P., Wang F., Chen G., Scott G., Wang G., Shabala S., Zhou M., Chen Z.-H. (2017) – QTLs for stomatal and photosynthetic traits related to salinity tolerance in barley – BMC Genomics 18(1): 1-13 – DOI:10.1186/s12864-016-3380-0  – https://www.infona.pl/resource/bwmeta1.element.springer-doi-10_1186-S12864-016-3380-0 – (On our blog : https://plantstomata.wordpress.com/2017/10/24/qtls-for-stomatal-traits-related-to-salinity-tolerance/)

Liu X., Mak M., Babla M., Wang F., Chen G., Veljanoski F., Wang G., Shabala S., Zhou M., Chen Z.-H. (2014) Linking stomatal traits and expression of slow anion channel genes HvSLAH1 and HvSLAC1 with grain yield for increasing salinity tolerance in barley – Frontiers in Plant Science 5  – http://dx.doi.org/10.3389/fpls.2014.00634 – http://dx.doi.org/10.3389/fpls.2014.00634 – http://journal.frontiersin.org/article/10.3389/fpls.2014.00634/abstract – (On our blog : https://plantstomata.wordpress.com/2016/07/29/16910/)

Liu X., Suarez D. L. (2021) – Lima Bean Growth, Leaf Stomatal and Nonstomatal Limitations to Photosynthesis, and 13C Discrimination in Response to Saline Irrigation – 146(2): – Journal of the American Society for Horticultural Science – https://doi.org/10.21273/JASHS04996-20https://journals.ashs.org/jashs/view/journals/jashs/146/2/article-p132.xml – (On our blog : https://plantstomata.wordpress.com/2022/02/08/leaf-stomatal-and-nonstomatal-limitations-to-photosynthesis/ )

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Liu X.-s., Liang C.-c., Hou S.-g., Wang X., Chen D.-h., Shen J.-l., Zhang W., Wang M. (2020) – The LRR-RLK Protein HSL3 Regulates Stomatal Closure and the Drought Stress Response by Modulating Hydrogen Peroxide Homeostasis – Front. Plant Sci. – https://doi.org/10.3389/fpls.2020.548034https://www.frontiersin.org/articles/10.3389/fpls.2020.548034/full – (On our blog : https://plantstomata.wordpress.com/2021/03/19/hsl3-was-concluded-to-participate-in-the-regulation-of-the-response-to-moisture-deficit-through-aba-induced-stomatal-closure/ )

Liu X. Y., Gao Q., Han M., Jin J. H. (2016) – Estimates of late middle Eocene pCO2 based on stomatal density of modern and fossil Nageia leaves – Clim. Past 12: 241–253 – doi:10.5194/cp-12-241-2016 – https://www.clim-past.net/12/241/2016/cp-12-241-2016.pdf – (On our blog : https://plantstomata.wordpress.com/2018/03/20/stomatal-density-for-estimates-of-late-middle-eocene-pco2/ )

Liu X. Y., Guo S. R., Xu Z. G., Jiao X. L., Tezuka T. (2011) – Regulation of chloroplast ultrastructure, cross-section anatomy of leaves, and morphology of stomata of cherry tomato by different light irradiations of light-emitting diodes – HortScience 46(2): 217-221 – https://doi.org/10.21273/HORTSCI.46.2.217https://journals.ashs.org/hortsci/view/journals/hortsci/46/2/article-p217.xml – (On our blog : https://plantstomata.wordpress.com/2020/09/08/morphology-of-stomata-by-different-light-irradiations-of-light-emitting-diodes/ )

Liu Y., Maierhofer T., Rybak K., Sklenar J., Breakspear A., Johnston M. G., Fliegmann J., Huang S., Roelfsema M. R. G., Felix G., Faulkner C., Menke F. L. H., Geiger D., Hedrich R. , Robatzek S. (2019) – Anion channel SLAH3 is a regulatory target of chitin receptor-associated kinase PBL27 in microbial stomatal closure – eLife 2019;8:e44474 – DOI: 10.7554/eLife.44474https://elifesciences.org/articles/44474?utm_source=miragenews&utm_medium=miragenews&utm_campaign=news – (On our blog : https://plantstomata.wordpress.com/2019/10/08/slah3-is-a-regulatory-target-of-chitin-receptor-associated-kinase-pbl27-in-microbial-stomatal-closure/ )

Liu Y., Mauve C., Lamothe‐Sibold M., Guérard F., Glab N., Hodges M., Jossier M. (2019) – Photorespiratory serine hydroxymethyltransferase 1 activity impacts abiotic stress tolerance and stomatal closure – Plant, Cell & Environment – https://doi.org/10.1111/pce.13595https://onlinelibrary.wiley.com/doi/abs/10.1111/pce.13595?af=R – (On our blog : https://plantstomata.wordpress.com/2019/07/08/shmt1-activity-impacts-abiotic-stress-tolerance-and-stomatal-closure/ )

Liu Y., Qin L., Han L., Xiang Y., Zhao D. (2015) – Overexpression of maize SDD1 (ZmSDD1) improves drought resistance in Zea mays L. by reducing stomatal density – Plant Cell Tiss. Organ Cult. 122: 147–159 – DOI: 10.1007/s11240-015-0757-8 – https://link.springer.com/article/10.1007/s11240-015-0757-8#citeas – (On our blog : https://plantstomata.wordpress.com/2018/10/31/overexpression-of-zmsdd1-improves-drought-resistance-by-reducing-stomatal-density/

Liu Y.-B., Li X.-R., Li M.-M., Liu D., Zhang W.-L. (2016) – Leaf (or assimilation branch) epidermal micromorphology of desert plant in arid and semiarid areas of China – Chinese Journal of Plant Ecology 40(11): 1189-1207- ISSN:1005-264X – http://jtp.cnki.net/bilingual/detail/html/ZWSB201611008 – (On our blog : https://plantstomata.wordpress.com/2020/04/15/the-main-epidermal-appendages-of-desert-plants-and-epidermal-structures-stomata-could-cooperate-with-each-other-to-improve-the-resistance-of-desert-plants-to-drought/ )

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Liu Y.-L., Xu S. S., Gao J, Pan S., Wang G. X. (2016) – Glucose- and mannose-induced stomatal closure is mediated by ROS production, Ca2+ and water channel in Vicia faba – Physiologia Plantarum 156: 252–261 – https://doi.org/10.1111/ppl.12353 – https://onlinelibrary.wiley.com/doi/abs/10.1111/ppl.12353 – (On our blog : https://plantstomata.wordpress.com/2018/05/28/glucose-and-mannose-induced-stomatal-closure/ )

Liu Z., Hou S., Rodrigues O., Wang P., Luo D., Munemasa S. Lei J., Liu J., Ortiz-Morea F. A., Wang X., Nomura K., Yin C., Wang H., Zhang W., Zhu-Salzman K., He S. Y., He P., Shan L. (2022) –  Phytocytokine signalling reopens stomata in plant immunity and water loss – Nature – https://doi.org/10.1038/s41586-022-04684-3https://www.nature.com/articles/s41586-022-04684-3#citeas – (On our blog : https://plantstomata.wordpress.com/2022/05/11/the-screw-nut-system-has-an-important-role-in-preventing-uncontrolled-stomatal-closure-caused-by-abiotic-and-biotic-stresses-to-optimize-plant-fitness/ )

Liu Z., Wang W., Zhang C.-G., Zhao J.-F., Chen Y.-L. (2017) – GUS Staining of Guard Cells to Identify Localised Guard Cell Gene Expression – Bio-protocol 7(14): e2446 – DOI: 10.21769/BioProtoc.2446 – https://bio-protocol.org/e2446 – (On our blog : https://plantstomata.wordpress.com/2018/01/17/gus-staining-of-guard-cells-stomata/ )

Liu Z., Zhou Y., Guo J., Li J., Tian Z., Zhu Z., Wang J., Wu R., Zhang B., Hu Y., Sun Y., Shangguan Y., Li W., Li T., Hu Y., Guo C., Rochaix J.-D., Miao Y., Sun X. (2020) – Global Dynamic Molecular Profiles of Stomatal Lineage Cell Development by Single-Cell RNA Sequencing – Biorxiv preprint – https://doi.org/10.1101/2020.02.13.947549https://www.biorxiv.org/content/10.1101/2020.02.13.947549v1.full.pdf – (On our blog : https://plantstomata.wordpress.com/2020/04/17/new-regulatory-mechanisms-during-development-of-stomatal-cell-lineage/ )

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Lu W., Deng M.,Guo F., Wang M., Zeng Z., Han N., Yang Y., Zhu M., Bian H. (2016) – Suppression of OsVPE3 Enhances Salt Tolerance by Attenuating Vacuole Rupture during Programmed Cell Death and Affects Stomata Development in Rice – Rice 9(1): 1-13 – DOI: 10.1186/s12284-016-0138-x  – https://www.infona.pl/resource/bwmeta1.element.springer-doi-10_1186-S12284-016-0138-X – (On our blog : https://plantstomata.wordpress.com/2017/10/11/osvpe3-plays-a-crucial-role-in-vacuole-mediated-pcd-and-in-stomatal-development-in-rice/)

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Lu Y., Duursma R. A., Medlyn B. E. (2016) – Optimal stomatal behaviour under stochastic rainfall – Journal of Theoretical Biology 394: 160-171 – https://doi.org/10.1016/j.jtbi.2016.01.003 –https://www.sciencedirect.com/science/article/pii/S0022519316000047?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/03/26/optimal-stomatal-behaviour-under-stochastic-rainfall/ )

Lu Y. Equiza M. A., Deng X., Tyree M. T. (2010) – Recovery of Populus tremuloides seedlings following severe drought causing total leaf mortality and extreme stem embolism – Physiol Plant. 140(3): 246-257 – doi: 10.1111/j.1399-3054.2010.01397.x – Epub 2010 Jul 27 – https://www.ncbi.nlm.nih.gov/pubmed/20618763 – (On our blog : https://plantstomata.wordpress.com/2019/08/30/stomatal-conductance-and-recovery-of-seedlings-following-severe-drought/ )

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