PHYSIO-BIBLIOGRAPHY W-Z

Waadt R., Manalansan B., Rauniyar N., Munemasa S., Booker M. A., Brandt B., Waadt C., Nusinow D. A., Kay S. A., Kunz H.-H.,  Schumacher K., DeLong A., Yates J. R., Schroeder J. I. (2015) – Identification of open stomata1-interacting proteins reveals interactions with sucrose non-fermenting1-related protein Kinases2 and with Type 2A protein phosphatases that function in abscisic acid responses – Plant Physiol. 169: 760–779 – doi: 10.1104/pp.15.00575 – http://www.plantphysiol.org/content/169/1/760 – (On our blog : https://plantstomata.wordpress.com/2018/02/02/the-roles-of-regulatory-pp2aa-subunits-and-catalytic-pp2ac-subunits-in-aba-responses/ )

Wada T., Tachibana T., Shimura Y., Okada K. (1997) – Epidermal cell differentiation in Arabidopsis determined by a Myb homolog – CPC Science 277: 1113–1116 –

Wagg S., Mills G., Hayes F., Wilkinson S., Davies W. J. (2013) – Stomata are less responsive to environmental stimuli in high background ozone in Dactylis glomerata and Ranunculus acris – Environmental Pollution 175: 82-91 – http://dx.doi.org/10.1016/j.envpol.2012.11.027 – https://www.sciencedirect.com/science/article/pii/S0269749112005052?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2018/01/31/stomatal-responses-and-ozone/ )

Waggoner P. E. (1964) – Decreasing Transpiration of Field Plants by Chemical Closure of Stomata – Nature 201(4914): 97-98 – DOI: 10.1038/201097b0https://ui.adsabs.harvard.edu/abs/1964Natur.201…97W/abstract – (On our blog : https://plantstomata.wordpress.com/2021/11/19/the-effect-of-chemical-closure-of-stomata-on-transpiration-by-a-population-of-plants-in-the-field/ )

Waggoner P. E. (1965) – Relative effectiveness of change in upper and lower stomatal openings – Crop Sci. 5: 291 –https://dl.sciencesocieties.org/publications/cs/abstracts/5/4/CS0050040291?access=0&view=pdf – (On our blog : https://plantstomata.wordpress.com/2017/09/16/effectiveness-of-change-in-upper-and-lower-stomatal-openings/ )

Waggoner P. E., Bravdo B.-A. (1967) – Stomata and the hydrologic cycle – Proc. Nat. Acad. Sci. U. S. 57: 1096-1102 – https://doi.org/10.1073/pnas.57.4.1096https://www.pnas.org/content/57/4/1096 – (On our blog : https://plantstomata.wordpress.com/2021/11/16/95496/ )

Waggoner P. E., Monteith J. L., Szeicz G. (1964) – Decreasing Transpiration of Field Plants by Chemical Closure of Stomata – Nature 201: 97–98 – doi:10.1038/201097b0 – https://www.nature.com/articles/201097b0 – (On our blog : https://plantstomata.wordpress.com/2018/01/05/chemical-closure-of-stomata-and-the-decrease-of-transpiration/ )

Waggoner P. E., Pallas J. E. Jr (xxxx) – Saving the water spent by plants – https://naldc.nal.usda.gov/download/IND43895178/PDF – (On our blog : https://plantstomata.wordpress.com/2021/11/15/saving-the-water-spent-by-plants/ )

Waggoner P. E., Simmonds N. W. (1966) – Stomata and transpiration of droopy potatoes – Plant Physiol. 41: 1268-1271 – DOI: 10.1104/pp.41.8.1268https://pdfs.semanticscholar.org/6575/fa8a46403a7b552fd9ebf98f4e497bc2cf4c.pdf – (On our blog : https://plantstomata.wordpress.com/2019/06/04/stomata-and-transpiration-of-droopy-potatoes/ )

Waggoner P. E., Turner N. C., (2020) – Transpiration and its Control by Stomata in a Pine Forest – Bull Conn Agric Expt Sta No. 726, 87p. – DOI: 10.13140/RG.2.2.18910.38727https://www.researchgate.net/publication/339999015_Waggoner_and_Turner_1971_Transpiration_and_its_Control_by_Stomata_in_a_Pine_Forest_Bull_Conn_Agric_Expt_Sta_No_726_87p – (On our blog : https://plantstomata.wordpress.com/2021/10/27/transpiration-and-its-control-by-stomata-2/ )

Waggoner P. E., Zelitch I. (1965) – Transpiration and the stomata of leaves – Science 150(3702): 1413-1420 – DOI: 10.1126/science.150.3702.1413 http://science.sciencemag.org/content/150/3702/1413 – (On our blog : https://plantstomata.wordpress.com/2018/01/06/stomata-and-transpiration/ )

Wagner F. (1998) – The influence of environment on the stomatal frequency in BetulaPhD Thesis – LPP Contributions Series no.9, LPP Foundation, 102p. (summary: www.bio.uu.nl/~palaeo/Personeel/Rike/Rikew.htm)

Wagner F., Aaby B., Visscher H. (2002) – Rapid atmospheric CO2 changes associated with the 8,200-years-B.P. cooling event – PNAS  99(19): 12011-12014 – https://doi.org/10.1073/pnas.182420699https://www.pnas.org/content/99/19/12011 – (On our blog : https://plantstomata.wordpress.com/2020/08/13/quantification-of-the-stomatal-frequency-signal-corroborates-a-distinctive-temperature-co2-correlation/ )

Wagner F., Below R., De Klerk P., Dilcher D. L., Joosten H., Kürschner W. M., Visscher H. (1996) – A natural experiment on plant acclimation: lifetime stomatal frequency response of an individual tree to annual atmospheric CO2 increase – Proceedings of the National Academy of Sciences of the United States of America 93: 11705-11708 – https://doi.org/10.1073/pnas.93.21.11705 –https://www.pnas.org/content/93/21/11705 – (On our blog : https://plantstomata.wordpress.com/2019/02/19/lifetime-stomatal-frequency-response-to-annual-atmospheric-co2-increase/ )

Wagner F., Dilcher D. L., Visscher H. (2005) – Stomatal frequency responses in hardwood‐swamp vegetation from Florida during a 60‐year continuous CO2 increase – American Journal of Botany 92(4): – https://doi.org/10.3732/ajb.92.4.690https://bsapubs.onlinelibrary.wiley.com/doi/full/10.3732/ajb.92.4.690 – (On our blog : https://plantstomata.wordpress.com/2020/05/20/stomatal-frequency-responses-in-hardwood%e2%80%90swamp-vegetation/ )

Wagner-Cremer F., Visscher H., Kurschner W. M., Dilcher D. L. (2007) – Influence of ontogeny and atmospheric CO2 on stomata parameters of Osmunda regalis – Advances in Angiosperm Paleobotany and Paleoclimatic Reconstruction 258: 183–189 – ( CFS Courier Forschungsinstitut Senckenberg)

Waidyarathne P., Samarasinghe S. (2018) – Boolean Calcium Signalling Model Predicts Calcium Role in Acceleration and Stability of Abscisic Acid-Mediated Stomatal Closure – Scientific Reports 8, Article number: 17635 (2018)  – https://www.nature.com/articles/s41598-018-35872-9 – (On our blog : https://plantstomata.wordpress.com/2019/01/11/calcium-role-in-acceleration-and-stability-of-aba-mediated-stomatal-closure/ )

Waisel Y., Bokgeb G. A., Kozlowski T. T. (1969) – Effect of phenylmercuric acetate on stomatal movement and transpiration of exscised Betula papyrijera Marsh leaves – Plant Physiol. 44: 685-690 –

Wakeel A., Wang L., Xu M. (2021) – SPEECHLESS and MUTE Mediate Feedback Regulation of Signal Transduction during Stomatal Development – Plants 2021, 10: 432 – https://doi.org/10.3390/plants10030432, file:///C:/Users/wille/Downloads/plants-10-00432-v2%20(1).pdf – (On our blog : https://plantstomata.wordpress.com/2021/07/09/the-feedback-mechanisms-driven-by-spch-and-mute-in-the-regulation-of-epf2-and-the-erecta-family-and-intersections-of-the-molecular-mechanisms-for-fate-determination-of-stomatal-lineage-cells/ )

Walker D. A., Zelitch I. 1963) – Some effects of metabolic inhibitors, temperature, and anaeroobic conditions on stomatal movement – Plant Physiology 38: 390-396 – PMCID: PMC549940 – PMID: 16655803 –https://www.ncbi.nlm.nih.gov/pmc/articles/PMC549940/ – (On our blog : https://plantstomata.wordpress.com/2019/02/19/biochemical-reactions-responsible-for-stomatal-movements-occur-simultaneously-in-the-light/ )

Wall G. W., Adam N. R., Brooks T. J., Kimball B. A., Pinter P. J., LaMorte R. L., Adamsen F. J., Hunsaker D. J., Wechsung G., Wechsung F., Gossman-Clarke S., Leavitt S., Matthias A. D., Webber A. N. (2000) –  Acclimation response of spring wheat in a free-air CO2 enrichment (FACE) atmosphere with variable soil nitrogen regimes. 2. Net assimilation and stomatal conductance of leaves – Photosynth. Res. 66: 79-95 – https://doi.org/10.1023/A:1010646225929https://link.springer.com/article/10.1023/A:1010646225929#citeas – (On our blog : https://plantstomata.wordpress.com/2019/02/19/net-assimilation-and-stomatal-conductance/ )

Wallace A., Deutsch A. (1968) – Phosphorus deficiency decreases stomatal activity and water use of plants – Calif Agr 22(8): 15-16 – https://calag.ucanr.edu/Archive/?article=ca.v022n08p15 – (On our blog : https://plantstomata.wordpress.com/2021/11/14/phosphorus-deficiency-decreases-stomatal-activity/ )

Wallace J., Roberts J., Sivakumar M. (1990) – The estimation of transpiration from sparse dryland millet using stomatal conductance and vegetation area indices – Agric. For. Meteorol. 51: 35–49 – https://doi.org/10.1016/0168-1923(90)90040-Dhttps://www.sciencedirect.com/science/article/abs/pii/016819239090040D?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2022/04/20/the-estimation-of-transpiration-using-stomatal-conductance-and-vegetation-area-indices/ )

Wallheimer B. (2011) – Gene helps plants use less water without biomass loss – Purdue University News Service – https://www.purdue.edu/newsroom/research/2011/110111MickelbartGene.html – (On our blog : https://plantstomata.wordpress.com/2020/12/07/gene-helps-plants-use-less-water-without-biomass-loss/ )

Wallin G. (1990) – On the impact of tropospheric ozone on photosynthesis and stomatal conductance of Norway spruce, Picea abies (L.) Karst. – Ph. D. Thesis, University of Göteborg

Wallin G., Ottosson S., Selldén G. (1992) – Long term exposure of Norway spruce, Picea abies(L.) Karst., to ozone in open-top chambers – IV. Effects on the stomatal and the non-stomatal limitation of photosynthesis and on the carboxylation efficiency – New Phytol. 121(3): – https://doi.org/10.1111/j.1469-8137.1992.tb02939.x – https://nph.onlinelibrary.wiley.com/doi/full/10.1111/j.1469-8137.1992.tb02939.x – (On our blog : https://plantstomata.wordpress.com/2019/02/19/effects-of-ozone-on-the-stomatal-and-the-non-stomatal-limitation-of-photosynthesis/ )

Wallin G., Skärby L. (1992) – The influence of ozone on the stomata1 and non-stomatal limitation of photosynthesis in Norway spruce, Picea abies (L.) Karst, exposed to soil moisture deficit – Trees, Structure and Function 6: 128-136 – https://link.springer.com/article/10.1007/BF00202428 – (On our blog : https://plantstomata.wordpress.com/2018/07/10/the-influence-of-ozone-on-the-stomatal-and-non-stomatal-limitation-of-photosynthesis/ )

Walter J., Rastorfer J. R., Eigsti O. J. (1976) – Comparison of chlorophyll contents hill reactions number of chloroplasts in guard cells and lengths of guard cells in diploid and tetraploid plants of Tradescantia ohiensis – Transactions of the Illinois State Academy of Science 69(2): 218 – https://eurekamag.com/research/026/294/026294419.php – (On our blog : https://plantstomata.wordpress.com/2022/01/07/number-of-chloroplasts-in-stomatal-guard-cells-and-lengths-of-guard-cells-in-diploid-and-tetraploid-plants/ )

Walter K. (2018) – Scientists Manipulate Crops to Need Less Water – R&D magazine 2018-03-06 – https://www.rdmag.com/article/2018/03/scientists-manipulate-crops-need-less-water – (On our blog : https://plantstomata.wordpress.com/2018/03/07/increased-psbs-expression-allows-crop-plants-to-be-more-conservative-with-water-use-triggering-stomata-to-close/ )

Walton B. C., Galson E., Harrison M. A. (1977) – The Relationship between Stomatal Resistance and Abscisic-acid Levels in Leaves of Water-stressed Bean Plants – Planta 133: 145-148 –

Walton P. D. (1974) –  The genetics of stomatal length and frequency in clones of Bromus inermis and the relationships between these traits and yield – Canadian Journal of Plant Science 54: 749-754 – https://doi.org/10.4141/cjps74-127 – http://www.nrcresearchpress.com/doi/10.4141/cjps74-127 – (On our blog : https://plantstomata.wordpress.com/2019/02/19/the-importance-of-stomatal-size-and-frequency-in-a-breeding-program-in-relation-to-agronomic-practices/ )

Wan X., Landhäusser S. M., Zwiazek J. J., Lieffers V. J. (2004) – Stomatal conductance and xylem sap properties of aspen (Populus tremuloides) in response to low soil temperature – Physiologia Plantarum 122: 79–85 – https://doi.org/10.1111/j.1399-3054.2004.00385.x –https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1399-3054.2004.00385.x – (On our blog : https://plantstomata.wordpress.com/2019/02/25/stomatal-conductance-and-xylem-sap-properties-in-response-to-low-soil-temperature/ )

Wan X., Zwiazek J. J. (2001) – Root water flow and leaf stomatal conductance in aspen ( Populus tremuloides ) seedlings treated with abscisic acid – Planta 213: 741-747 – DOI 10.1007/s004250100547Root_water_flow_and_leaf_stomatal_conduc.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/20/75564/ )

Wang B. X., Zeng Y. H., Wang D. Y., Zhao R., Xu X. (2010) – Responses of leaf stomata to environmental stresses in distribution and physiological characteristics – Agricultural Research in the Arid Areas 28: 122-126 –


[ 王碧霞, 曾永海, 王大勇, 赵蓉, 胥晓 (2010). 叶片气孔分布及生理特征对环境胁迫的响应. 干旱地区农业研究, 28,122-126.]

Wang C., He J., Zhao T.-H., Cao Y., Wang G., Sun B., Yan X., Guo W., Li M.-H. (2019) – The Smaller the Leaf Is, the Faster the Leaf Water Loses in a Temperate Forest – Front. Plant Sci., 04 February 2019 – https://doi.org/10.3389/fpls.2019.00058https://www.frontiersin.org/articles/10.3389/fpls.2019.00058/full – (On our blog : https://plantstomata.wordpress.com/2019/12/29/evidences-for-leaf-size-in-leaf-temperature-regulation-in-dry-environment-with-strong-radiation/ )

Wang C., Hu H., Qin X., Zeise B., Xu D., Rappel W. J., Boron W. F., Schroeder J. I. (2016) – Reconstitution of CO2 Regulation of SLAC1 Anion Channel and Function of CO2-Permeable PIP2;1 Aquaporin as CARBONIC ANHYDRASE4 Interactor – Plant Cell. 28(2): 568-582 – doi: 10.1105/tpc.15.00637 – Epub 2016 Jan 13 – https://www.ncbi.nlm.nih.gov/pubmed/26764375 – (On our blog : https://plantstomata.wordpress.com/2019/09/08/slac1-as-a-bicarbonate-responsive-protein-contributing-to-co2-regulation-of-s-type-anion-channels-in-stomata/ )

Wang C.,  Li Y., Cui D., Su H. (1997) – Study on the doubling effect of colchicine on leaves in vitro of apple seedlings – Acta Agriculturae Nucleatae Sinica 11(1): 21-25 – ISSN 1000-8551 – https://inis.iaea.org/search/search.aspx?orig_q=RN:28046760 – (On our blog : https://plantstomata.wordpress.com/2022/09/18/study-on-the-stomata-and-the-doubling-effect-of-colchicine-on-leaves-in-vitro-of-apple-seedlings/ )

Wang C., Liu S., Dong Y., Zhao Y., Geng A., Xia X., et al. (2016) – PdEPF1 regulates water-use efficiency and drought tolerance by modulating stomatal density in poplar -Plant Biotechnol. J. 14: 849–860 – DOI:  10.1111/pbi.12434 –  https://www.ncbi.nlm.nih.gov/pubmed/26228739 – (On our blog : https://plantstomata.wordpress.com/2019/02/25/pdepf1-is-modulating-stomatal-density/ )

Wang C., Zhang J., Wu J., Brodsky D. E., Schroeder J. I. (2018) – Cytosolic malate and oxaloacetate activate S‐type anion channels in Arabidopsis guard cells – New Phytol. Online Version of Record  – https://doi.org/10.1111/nph.15292 – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.15292?af=R – (On our blog : https://plantstomata.wordpress.com/2018/07/12/cytosolic-organic-anions-function-in-guard-cell-plasma-membrane-ion-channel-regulation-of-stomata/ )

Wang C. Y., Pang Y. M., Li M. S., et al. (2013) – Effects of drought stress on soybean stomatal characteristics and photosynthetic parameter – Journal of Agricultural Science and Technology 15(1): 109-115 – http://d.old.wanfangdata.com.cn/Periodical/zgnykjdb201301024

Wang F., Jia J., Wang Y., Wang W., Chen Y., Liu T., Shang Z. (2014) – Hyperpolization-activated Ca2+ channels in guard cell plasma membrane are involved in extracellular ATP-promoted stomatal opening in Vicia faba – J. Plant. Physiol. 171: 1241–1247 – https://doi.org/10.1016/j.jplph.2014.05.007https://www.sciencedirect.com/science/article/abs/pii/S0176161714001424?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2022/02/21/eatp-may-promote-stomatal-opening-via-reactive-oxygen-species-that-regulate-guard-cell-plasma-membrane-ca2-channels/ )

Wang F., Robson T. M., Casal J. J., Shapiguzov A., Aphalo P. J. (2020) – Contributions of cryptochromes and phototropins to stomatal opening through the day – Functional Plant Biology 47(3): 226-238 – https://doi.org/10.1071/FP19053https://www.publish.csiro.au/fp/FP19053 – (On our blog : https://plantstomata.wordpress.com/2021/05/09/90752/ )

Wang F., Xin X., Wei H., Qiu X., Liu B. (2020) – In Vitro Regeneration, Ex Vitro Rooting and Foliar Stoma Studies of Pseudostellaria heterophylla
(Miq.) Pax – Agronomy 10: 949 – doi:10.3390/agronomy10070949file:///C:/Users/wille/Downloads/agronomy-10-00949.pdf – (On our blog : https://plantstomata.wordpress.com/2021/04/17/stomata-studies-of-pseudostellaria-heterophylla/ )

Wang F.-F., Lian H.-L., Kang C.-Y., Yang H.-Q. (2010) – Phytochrome B Is Involved in Mediating Red Light-Induced Stomatal Opening in Arabidopsis thaliana – Molecular Plant 3(1): 246-259 – https://doi.org/10.1093/mp/ssp097https://www.sciencedirect.com/science/article/pii/S167420521460410X – (On our blog : https://plantstomata.wordpress.com/2018/12/03/phyb-and-cry-might-regulate-stomatal-opening-by-regulating-myb60-expression/

Wang G. X.,  Zhang J.,  Liao J.-X.,  Wang J.-L. (2001) – Hydropassive evidence and effective factors in stomatal oscillations of Glycyrrhiza inflata under desert conditions – Plant Science 160: 1007-1013 – https://doi.org/10.1016/S0168-9452(01)00344-2 –https://www.sciencedirect.com/science/article/pii/S0168945201003442?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/04/07/hydropassive-evidence-and-effective-factors-in-stomatal-oscillations-under-desert-conditions/ )

Wang H. Z., Han L., Xu Y. L., Niu J. L. (2015) – Model analysis of the stomatal conductance response to light in Populus pruinosa at different temperatures in the Taklimakan desert – Ecology and Environmental Sciences 24: 741-748 – [ 王海珍, 韩路, 徐雅丽, 牛建龙 (2015). 不同温度下灰胡杨叶片气孔导度对光强响应的模型分析. 生态环境学报, 24,741-748.]

Wang H., Clarke J. M. (1993) – Relationship of excised-leaf water loss and stomatal frequency in wheat / Rapport entre la déperdition d’eau sur feuilles excisées et la fréquence stomatique chez le blé. – Can. J. Plant. Sci. 73(1): 93-99 – https://www.nrcresearchpress.com/doi/pdfplus/10.4141/cjps93-012 – (On our blog : https://plantstomata.wordpress.com/2020/06/20/excised-leaf-water-loss-and-stomatal-frequenc/ )

Wang H., Clarke J. M. (1993) – Genotypic, intraplant, and environmental variation in stomatal frequency and size in wheat – Can. J. Plant. Sci. 73(3): 671-678 – https://doi.org/10.4141/cjps93-088 – http://www.nrcresearchpress.com/doi/10.4141/cjps93-088 – (On our blog : https://plantstomata.wordpress.com/2018/10/06/stomatal-frequency-and-size-in-wheat/ )

Wang H., Guo S., Qiao X., Guo J., Li Z., Zhou Y., Bai S., Gao Z., Wang D., Wang P., Galbraith D. W., Song C. P. (2019) – BZU2/ZmMUTE controls symmetrical division of guard mother cell and specifies neighbor cell fate in maize – PLoS Genet. 15(8):e1008377 – doi: 10.1371/journal.pgen.1008377 – PMID: 31465456 – PMCID: PMC6738654 – https://pubmed.ncbi.nlm.nih.gov/31465456/ – (On our blog : https://plantstomata.wordpress.com/2021/03/30/89224/ )

Wang H., Ngwenyama N., Liu Y., Walker J. C., Zhang S. (2007) – Stomatal development and patterning are regulated by environmentally responsive mitogen-activated protein kinases in Arabidopsis – Plant Cell 19: 63–73 – doi: 10.1105/tpc.106.048298 – (On our blog : https://plantstomata.wordpress.com/2015/03/14/environmentally-responsive-mitogen-activated-protein-kinases/)

Wang H., Wei Z., Li J., Wang X. (2017) – 9 – Brassinosteroids – In : Hormone Metabolism and Signaling in Plants 2017, Pages 291-326 – https://doi.org/10.1016/B978-0-12-811562-6.00009-8https://www.sciencedirect.com/science/article/pii/B9780128115626000098 – (On our blog : https://plantstomata.wordpress.com/2021/02/08/br-regulated-plant-developmental-processes-include-stomatal-development/ )

Wang H., Yan S., Xin H., Huang W., Zhang H., Teng S., Yu Y.-C., Fernie A. R., Lu X., Li P., Li S., Zhang C., Ruan Y.-L., Chen L.-Q, Lang Z. (2019) – A Subsidiary Cell-Localized Glucose Transporter Promotes Stomatal Conductance and Photosynthesis – Plant Cell – https://doi.org/10.1105/tpc.18.00736http://www.plantcell.org/content/31/6/1328 – (On our blog : https://plantstomata.wordpress.com/2019/06/14/cst1-as-a-missing-link-in-the-feedback-regulation-of-stomatal-movement/ )

Wang H.-B., Wang X.-C., Chen J., Cao M., Li Y.-Y. (1997) – Relationship of stomata sensitivity to ABA and ABA-binding proteins on the plasmalemma of guard cells in Vicia faba – Acta Bot Sin. 39: 126-129 (in Chinese with English abstract) –

Wang J., Lu W., Tong Y., Yang Q. (2016) – Leaf Morphology, Photosynthetic Performance, Chlorophyll Fluorescence, Stomatal Development of Lettuce (Lactuca sativa L.) Exposed to Different Ratios of Red Light to Blue Light – Front. Plant Sci., 10 March 2016 | http://dx.doi.org/10.3389/fpls.2016.00250 – http://journal.frontiersin.org/article/10.3389/fpls.2016.00250/full – (On our blog : https://plantstomata.wordpress.com/2016/03/28/8946/ )

Wang J., Shi L., Song S., Tian J., Kang X. (2013) – Tetraploid production through zygotic chromosome doubling in Populus – Silva Fennica 47(2): article id 932 – https://doi.org/10.14214/sf.932https://silvafennica.fi/article/932/ref/3 – (On our blog : https://plantstomata.wordpress.com/2022/01/26/size-and-frequency-of-leaf-stomata-between-tetraploid-and-diploid-plants-were-significantly-different/ )

Wang J., Wen X. (2022) – Excess radiation exacerbates drought stress impacts on stomatal conductance along aridity gradients – European Geosciences Union: Biogeosciences (preprint currently under review for the journal BG) – https://doi.org/10.5194/bg-2022-50https://bg.copernicus.org/preprints/bg-2022-50/ – (On our blog : https://plantstomata.wordpress.com/2022/03/19/the-need-to-integrate-multiple-stressors-and-plant-properties-to-determine-spatial-variability-in-stomatal-conductance-gs/ )

Wang J., Wen X., Lyu S., Guo Q. (2021) – Soil properties mediate ecosystem intrinsic water use efficiency and stomatal conductance via taxonomic diversity and leaf economic spectrum – Science of the Total Environment  (IF7.963) – DOI: 10.1016/j.scitotenv.2021.146968https://en.x-mol.com/paper/article/1382786176436428800https://www.sciencedirect.com/science/article/abs/pii/S0048969721020386 – (On our blog : https://plantstomata.wordpress.com/2022/03/30/complex-feedbacks-that-regulate-intrinsic-water-use-efficiency-iwue-and-stomatal-conductance-gs-at-ecosystem-level/ )

Wang K., Gao Y., Li S., Zhang M., Wu Z., Liu L., Sun H., Li C., Zhang Y. (2019) – Response of leaf stomata and photosynthetic parameters to short-term drought stress in cotton (Gossypium hirsutum L.) – Chinese Journal of Eco-Agriculture 27(6): 901-907 – doi: 10.13930/j.cnki.cjea.180928http://www.ecoagri.ac.cn/en/article/doi/10.13930/j.cnki.cjea.180928?utm_source=TrendMD&utm_medium=cpc&utm_campaign=Chinese_Journal_of_Eco-Agriculture_TrendMD_1 – (On our blog : https://plantstomata.wordpress.com/2022/03/23/the-simulated-drought-induced-by-peg-6000-may-result-in-cotton-stomatal-closure-and-an-increase-in-stomatal-density/ )

Wang L., Li Q.-T., Lei Q., Feng C., Zheng X., Zhou F., Li L., Liu X., Wang Z., Kong J. (2017) – Ectopically expressing MdPIP1;3, an aquaporin gene, increased fruit size and enhanced drought tolerance of transgenic tomatoes – BMC Plant Biol. 17(1): 246 – doi: 10.1186/s12870-017-1212-2 – PMID: 29258418 – PMCID: PMC5735821 – https://pubmed.ncbi.nlm.nih.gov/29258418/ – (On our blog : https://plantstomata.wordpress.com/2022/09/08/enhanced-drought-tolerance-of-transgenic-tomatoes-partially-via-reduced-water-loss-controlled-by-stomata-closure-in-leaves/ )

Wang M., Feifei Y., Hao H., Zhang Y., Zhao H., Guo A., Hu J., Zhou X., Xie C. (2013) – BolOST1, an ortholog of Open Stomata 1 with alternative splicing products in Brassica oleracea, positively modulates drought responses in plants. – Biochem. Biophys. Res. Commun. 442: 214–220 – doi: 10.1016/j.bbrc.2013.11.032 – https://www.sciencedirect.com/science/article/pii/S0006291X13019141 – (On our blog : https://plantstomata.wordpress.com/2018/07/10/bolost1-is-a-functional-snrk2-type-protein-kinase-positively-modulates-drought-responses-stomata/ )

Wang M., Ji Q., Liu P., Liu Y. (2022) – Guarding and hijacking: stomata on the move – Trends in Plant Science – https://doi.org/10.1016/j.tplants.2022.05.004https://www.cell.com/trends/plant-science/fulltext/S1360-1385(22)00142-X – (On our blog : https://plantstomata.wordpress.com/2022/05/26/106804/ )

Wang M., Wei H., Jeong B. R. (2021) – Lighting Direction Affects Leaf Morphology, Stomatal Characteristics, and Physiology of Head Lettuce (Lactuca sativa L.) – Int. J. Mol. Sci. 22(6): 3157 – https://doi.org/10.3390/ijms22063157https://www.mdpi.com/1422-0067/22/6/3157/htm – (On our blog : https://plantstomata.wordpress.com/2021/12/16/the-lighting-direction-has-a-profound-effect-on-the-morphological-characteristics-of-lettuce/ )

Wang M. H., Wang J. R., Zhang X. W., Zhang A. P., Sun S., Zhao C. M. (2019) – Phenotypic plasticity of stomatal and photosynthetic features of four Picea species in two contrasting common gardens – AoB Plants 11(4): plz034 – doi: 10.1093/aobpla/plz034https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6621916/ – (On our blog : https://plantstomata.wordpress.com/2019/10/09/phenotypic-plasticity-of-stomatal-and-photosynthetic-features/ )

Wang P., Dong F., Song C.-P., (2001) – Requirement for increasing production of hydrogen peroxide in salicylic acid induced stomatal closure in Vicia faba guard cells – Plant Biology (Rockville) : 36 – https://eurekamag.com/research/035/653/035653794.php

Wang P., Du Y., Hou Y. J., Zhao Y., Hsu C. C., Yuan F., et al. (2015) – Nitric oxide negatively regulates abscisic acid signaling in guard cells by S-nitrosylation of OST1. Proc. Natl. Acad. Sci. U.S.A. 112: 613–618 – doi: 10.1073/pnas.1423 481112 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299189/ – (On our blog : https://plantstomata.wordpress.com/2018/07/10/nitric-oxide-negatively-regulates-aba-signaling-in-stomata/ )

Wang P., Du Y., Zhao X., Miao Y., Song C.-P. (2012) – The MPK6-ERF-ROSE7/GCC-box complex modulates oxidative gene transcription and ROS signaling in Arabidopsis thaliana – Presentation at New Phytologist Symposium Nr. 29 on Stomata 2012 –https://www.newphytologist.org/app/webroot/img/upload/files/29thNPSAbstractBook.pdf – (On our blog : https://plantstomata.wordpress.com/2018/01/11/the-mpk6-erf-rose7-gcc-box-complex-in-stomata/ )

Wang Q., He Q., Zhou G. (2018) – Applicability of common stomatal conductance models in maize under varying soil moisture conditions – Science of The Total Environment 628–629: 141-149 – ISSN 0048-9697 –
https://doi.org/10.1016/j.scitotenv.2018.01.291
https://www.sciencedirect.com/science/article/pii/S0048969718303309 – (On our blog : https://plantstomata.wordpress.com/2022/05/05/a-basis-for-selecting-appropriate-stomatal-conductance-models-under-drought-conditions/ )

Wang P., Song C. P. (2008) – Guard-cell signalling for hydrogen peroxide and abscisic acid. – New Phytol. 178: 703–718 – doi: 10.1111/j.1469-8137.2008.02431.x – https://www.ncbi.nlm.nih.gov/pubmed/18373649 – (On our blog : https://plantstomata.wordpress.com/2018/07/11/points-of-connection-between-aba-and-h2o2-signalling-in-stomata/ )

Wang R., Yu G., He N., Wang Q., Zhao N., Xu Z., Ge J. (2014) – Elevation-Related Variation in Leaf Stomatal Traits as a Function of Plant Functional Type: Evidence from Changbai Mountain, China. – PLoS ONE 9(12): e115395 – https://doi.org/10.1371/journal.pone.0115395https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0115395 – (On our blog : https://plantstomata.wordpress.com/2021/09/18/elevation-related-patterns-of-stomatal-characteristics-in-leaves-are-primarily-a-function-of-pft/ )

Wang R., Yu G., He N., Wang Q., Zhao N., Xu Z., Ge J. (2015) – Latitudinal variation of leaf stomatal traits from species to community level in forests: linkage with ecosystem productivity – Scientific Reports 5, Article number: 14454 – https://www.nature.com/articles/srep14454 – (On our blog : https://plantstomata.wordpress.com/2019/04/01/new-insight-into-the-relationship-between-leaf-stomatal-traits-and-ecosystem-function/ )

Wang R. L., Yu G. R., He N. P., Wang Q. F, Zhao N., Xu Z. W. (2016) – Altitudinal variation in the covariation of stomatal traits with leaf functional traits in Changbai Mountain – Acta Ecologica Sinica 36: 2175-2184 –


[ 王瑞丽, 于贵瑞, 何念鹏, 王秋凤, 赵宁, 徐志伟 (2016). 气孔特征与叶片功能性状之间关联性沿海拔梯度的变化规律——以长白山为例. 生态学报, 36,2175-2184.]

Wang R. S., Pandey S., Li S., Gookin T. E., Zhao Z., Albert R., Assmann S. M. (2011) – Common and unique elements of the ABA-regulated transcriptome of Arabidopsis guard cells – BMC Genomics 12:216 – doi: 10.1186/1471-2164-12-216 – https://www.ncbi.nlm.nih.gov/pubmed/21554708 – (On our blog : https://plantstomata.wordpress.com/2018/07/10/elements-of-the-aba-regulated-transcriptome-of-stomata/ )

Wang S., Dong F., Sun D., Chen Y., Yan X., Jing R. ( 2018) – QTL analysis for stomatal density and size in wheat spike organ – Emirates Journal of Food and Agriculture. 30(3): 173-179 – doi: 10.9755/ejfa.2018.v30.i3.1636https://www.researchgate.net/publication/324649827_QTL_analysis_for_stomatal_density_and_size_in_wheat_spike_organ – (On our blog : https://plantstomata.wordpress.com/2019/09/20/qtl-analysis-for-stomatal-density-and-size/ )

Wang S., Jia S., Sun D., Fan H., Chang X., Jing R. (2016) – Mapping QTLs for stomatal density and size under drought stress
in wheat (Triticum aestivum L.) – Journal of Integrative Agriculture 15(9): 1955–1967 – https://core.ac.uk/download/pdf/82226104.pdf – (On our blog : https://plantstomata.wordpress.com/2020/04/12/mapping-qtls-for-stomatal-density-and-size-under-drought-stress-2/ )

Wang S., Sun J., Fan F., Tan Z., Zou Y., Lu D. (2016) – A Xanthomonas oryzae pv. oryzae effector, XopR, associates with receptor-like cytoplasmic kinases and suppresses PAMP-triggered stomatal closure – Sci. China Life Sci. 59: 897–905 – doi: 10.1007/s11427-016-5106-6https://www.frontiersin.org/articles/10.3389/fpls.2021.668797/full – (On our blog : https://plantstomata.wordpress.com/2021/11/09/xopr-likely-suppresses-plant-immunity-by-targeting-bik1-and-other-rlcks-and-it-suppresses-pamp-triggered-stomatal-closure/ )

Wang S., Yang Y., Trishchenko A. P., Barr A. G., Black T. A., McCaughey H., (2009) – Modeling the Response of Canopy Stomatal Conductance to Humidity – Journal of Hydrometeorology 10(2): 521-532 – https://doi.org/10.1175/2008JHM1050.1https://journals.ametsoc.org/view/journals/hydr/10/2/2008jhm1050_1.xml – (On our blog : https://plantstomata.wordpress.com/2021/02/18/new-models-to-improve-the-response-of-canopy-stomatal-conductance-to-humidity/ )

Wang S., Zhou Z., Rahiman R., Lee G. S. Y., Yeo Y. K., Yang X., Lau O. S. (2021) – Light regulates stomatal development by modulating paracrine signaling from inner tissues – Nat Commun 123403 – https://doi.org/10.1038/s41467-021-23728-2https://www.nature.com/articles/s41467-021-23728-2 – (On our blog : https://plantstomata.wordpress.com/2021/07/04/a-molecular-link-between-light-signaling-and-stomatal-development/ )

Wang S.-W., Li Y., Zhang X.-L., Yang H.-Q., Han X.-F., Liu Z.-H., Shang Z.-L., Asano T., Yoshioka Y., Zhang C.-G., Chen Y.-L. (2014)  – Lacking chloroplasts in guard cells of crumpled leaf attenuates stomatal opening: both guard cell chloroplasts and mesophyll contribute to guard cell ATP levels – Plant, Cell & Environment 37(9): 2201-2210 – https://doi.org/10.1111/pce.12297 – https://onlinelibrary.wiley.com/doi/abs/10.1111/pce.12297 – (On our blog : https://plantstomata.wordpress.com/2018/10/06/both-stomatal-chloroplasts-and-mesophyll-contribute-to-the-atp-source-for-h-extrusion-by-guard-cells/)

Wang W., Ganzeveld L., Rossabi S., Hueber J., Helmig D. (2020) – Measurement report: Leaf-scale gas exchange of atmospheric reactive trace species (NO2, NO, O3) at a northern hardwood forest in Michigan – Atmos. Chem. Phys. 20: 11287–11304 – https://doi.org/10.5194/acp-20-11287-2020https://acp.copernicus.org/articles/20/11287/2020/ – (On our blog : https://plantstomata.wordpress.com/2022/04/17/the-foliar-no2-and-o3-uptake-largely-followed-a-diurnal-cycle-correlating-with-that-of-the-leaf-stomatal-conductance/ )

Wang W., Liu Z., Bao L.-J., Zhang S.-S., Zhang C.-G., Li X., Li H.-X., Zhang X.-L., Bones A. M., Yang Z., Chen Y.-L. (2017) – The RopGEF2-ROP7/ROP2 pathway activated by phyB suppresses red light-induced stomatal opening – Plant Physiol 174: 717–731 – http://www.plantphysiol.org/content/174/2/717 – (On our blog : https://plantstomata.wordpress.com/2017/11/11/the-ropgef2-rop7-rop2-pathway-and-the-red-light-induced-stomatal-opening/)

Wang W.-H., Chen J., Liu T.-W., Chen J., Han A.-D., Simon M., Dong X.-J., He J.-X., Zheng H.-L. (2013) – Regulation of the calcium-sensing receptor in both stomatal movement and photosynthetic electron transport is crucial for water use efficiency and drought tolerance in Arabidopsis – Journal of Experimental Botany 65(1): 223–234 – doi:10.1093/jxb/ert362http://jxb.oxfordjournals.org/content/65/1/223.full.pdf+html – (https://plantstomata.wordpress.com/2016/12/10/cas-stomatal-movement-wue-and-drought-tolerance/ )

Wang W. H., He E. M., Chen J., Guo Y., Chen J., Liu X., Zheng H. L. (2016) – The
reduced state of the plastoquinone pool is required for chloroplast-mediated stomatal closure in response to calcium stimulation – Plant J. 86(2): 132-144 –
doi:10.1111/tpj.13154

Wang W. H., Yi X. Q., Han A. D., Liu T. W., Chen J., Wu F. H., Dong X. J., He J. X., Pei Z. M., Zheng H. L. (2011) – Calcium-sensing receptor regulates stomatal closure through hydrogen peroxide and nitric oxide in response to extracellular calcium in Arabidopsis – J. Exp. Bot. 63: 177–190 – doi: 10.1093/jxb/err259 – https://www.ncbi.nlm.nih.gov/pubmed/21940718 – (On our blog : https://plantstomata.wordpress.com/2018/07/11/a-hypothetical-model-whereby-ca2o-induces-h2o2-and-no-accumulation-in-stomata/ )

Wang W. N., Tarafdar J. C., Biswas P. (2013) – Nanoparticle synthesis and delivery by an aerosol route for watermelon plant foliar uptake – J Nanopart Res 15: 1417 – https://doi.org/10.1007/s11051-013-1417-8https://link.springer.com/article/10.1007/s11051-013-1417-8#citeas – (On our blog : https://plantstomata.wordpress.com/2022/09/29/certain-fractions-of-nanoparticles-generated-by-the-aerosol-process-could-enter-the-leaf-following-the-stomatal-pathway/ )

Wang X., Arora R., Horner H. T., Krebs S. L. (2008) – Structural Adaptations in Overwintering Leaves of Thermonastic and Nonthermonastic Rhododendron – American Society for Horticultural Science 133(6) – Doi:10.21273/JASHS.133.6.768https://www.researchgate.net/publication/252966100_Structural_Adaptations_in_Overwintering_Leaves_of_Thermonastic_and_Nonthermonastic_Rhododendron – (On our blog : https://plantstomata.wordpress.com/2019/08/06/stomata-in-thermonastic-and-nonthermonastic-rhododendron/ )

Wang X., Du T., Huang J., Peng S., Xiong D. (2018) – Leaf hydraulic vulnerability triggers the decline in stomatal and mesophyll conductance during drought in rice – J Exp Bot. 69(16): 4033-4045 – doi: 10.1093/jxb/ery188 – PMID: 29788146 – PMCID: PMC6054168 – https://pubmed.ncbi.nlm.nih.gov/29788146/ – (On our blog : https://plantstomata.wordpress.com/2021/11/26/the-decline-in-stomatal-and-mesophyll-conductance-during-drought-2/ )

Wang X., Wang Q., Nguyen P., Lin jC. (2014) – Chapter Seven – Cryptochrome-Mediated Light Responses in Plants – in Book The Enzymes 35: 167-189 – https://doi.org/10.1016/B978-0-12-801922-1.00007-5https://www.sciencedirect.com/science/article/pii/B9780128019221000075 – (On our blog : https://plantstomata.wordpress.com/2021/02/25/cryptochrome-mediated-light-responses-in-plants-stomata/ )

Wang X., Du T., Huang J., Peng S., Xiong D. (2018) – Leaf hydraulic vulnerability triggers the decline in stomatal and mesophyll conductance during drought in rice (Oryza sativa) – J Exp Bot 69: 4033–4045 – doi: 10.1093/jxb/ery188https://www.ncbi.nlm.nih.gov/pubmed/29788146 – (On our blog : https://plantstomata.wordpress.com/2019/05/15/the-decline-in-stomatal-and-mesophyll-conductance-during-drought/ )

Wang X. Q., Ullah H., Jones A. M., Assmann S. M. (2001) – G protein regulation of ion channels and abscisic acid signaling in Arabidopsis guard cells. -Science 292: 2070–2072 – doi: 10.1126/science.1059046 – https://www.ncbi.nlm.nih.gov/pubmed/11408655 – (On our blog : https://plantstomata.wordpress.com/2018/07/11/stomatal-opening-in-gpa1-plants-is-insensitive-to-inhibition-by-aba/

Wang X. Q., Wu W. H., Assmann S. M. (1998) – Differential responses of abaxial and adaxial guard cells of broad bean to abscisic acid and calcium – Plant Physiol 118: 1421–1429 – https://doi.org/10.1104/pp.118.4.1421http://www.plantphysiol.org/content/118/4/1421?ijkey=32fa9e41146ef1ce52eedd7701307e0dc0c4603c&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2019/01/11/osmo-sensitive-and-stretch-activated-ca2-channels-stomata-and-their-regulation-by-osmotic-changes-and-actin-dynamics/ )

Wang Y. (2009) – Enhanced plant photosynthesis and growth through manipulation of stomatal apertures – IAR Letter, 15 – http://www.aip.nagoya-u.ac.jp/en/public/nu_research/features/detail/0004138.html – (On our blog : https://plantstomata.wordpress.com/2018/11/26/overexpression-of-h-atpase-in-stomatal-guard-cells-enhances-plant-productivity/

Wang Y., Anderegg W. R. L., Venturas M. D., Trugman A. T., Yu K.,
Christian Frankenberg C. (2021)
– Optimization theory explains nighttime stomatal responses – New Phytologist – doi: 10.1111/nph.17267https://escholarship.org/content/qt80760038/qt80760038_noSplash_424551c0ada57ff84f901c20ccf49e92.pdf?t=r69w9s – (On our blog : https://plantstomata.wordpress.com/2022/04/01/why-do-plants-lose-water-at-night-and-how-to-model-it-at-large-scales/ )

Wang Y., Blatt M. R. (2011) – Anion channel sensitivity to cytosolic organic acids implicates a central role for oxaloacetate in integrating ion flux with metabolism in stomatal guard cells – Biochem. J. 439: 161–170 – doi: 10.1042/BJ20110845. – https://www.ncbi.nlm.nih.gov/pubmed/21745184 – (On our blog : https://plantstomata.wordpress.com/2019/02/25/a-central-role-for-oxaloacetate-in-integrating-ion-flux-with-metabolism-in-stomatal-guard-cells/ )

Wang Y., Chen Z. H. (2020) – Does Molecular and Structural Evolution Shape the Speedy Grass Stomata? – Frontiers in Plant Science 11 – DOI: 10.3389/fpls.2020.00333https://www.researchgate.net/publication/339727342_Does_Molecular_and_Structural_Evolution_Shape_the_Speedy_Grass_Stomata – (On our blog : https://plantstomata.wordpress.com/2020/04/29/the-differential-stomatal-morphology-developmental-mechanism-and-guard-cell-signaling-in-monocots-and-eudicots/ )

Wang Y., Chen X, Xiang C. (2007) –  Stomatal density and bio-water saving – Journal of Integrative Plant Biology 49(10): 1435–1444 – https://doi.org/10.1111/j.1672-9072.2007.00554.xhttps://onlinelibrary.wiley.com/doi/full/10.1111/j.1672-9072.2007.00554.x – (On our blog : https://plantstomata.wordpress.com/2018/07/12/genes-regulating-stomatal-density-and-the-role-of-stomatal-density-in-plant-water-use-efficiency/ )

Wang Y., Chen Z. H., Zhang B., Hills A., Blatt M. R. ( 2013) – PYR/PYL/RCAR abscisic acid receptors regulate K+ and Cl channels through reactive oxygen species‐mediated activation of Ca2+ channels at the plasma membrane of intact Arabidopsis guard cells – Plant Physiol 163: 566– 577 – DOI: 10.1104/pp.113.219758 –https://www.ncbi.nlm.nih.gov/pubmed/23899646?dopt=Abstract – (On our blog : https://plantstomata.wordpress.com/2019/03/22/pyr-pyl-rcar-receptor-coupling-to-the-activation-by-aba-of-plasma-membrane-ca2-channels-through-ros-affecting-ca2i-and-its-regulation-of-stomatal-closure/ )

Wang Y., Gehring C. A., Irving H. R. (2011) – Plant natriuretic peptides are apoplastic and paracrine stress response molecules – Plant and Cell Physiology 52(5): 837–850 – doi:10.1093/pcp/pcr036https://repository.kaust.edu.sa/handle/10754/561750 – (On our blog : https://plantstomata.wordpress.com/2022/09/13/atpnp-a-modulates-the-effects-of-aba-on-stomata/ )

Wang Y., Hills A., Blatt M. R. ((2014) – Systems analysis of guard cell membrane transport for enhanced stomatal dynamics and water use efficiency – Plant Physiology 164: 1593-1599 – https://doi.org/10.1104/pp.113.233403http://www.plantphysiol.org/content/164/4/1593 – (On our blog : https://plantstomata.wordpress.com/2019/09/26/systems-analysis-of-guard-cell-membrane-transport-for-enhanced-stomatal-dynamics/ )

Wang Y., Hills A., Vialet-Chabrand S., Papanatsiou M., Griffiths H., Rogers S., Lawson T., Lew V. L., Blatt M. R. (2017) – Unexpected Connections between Humidity and Ion Transport Discovered Using a Model to Bridge Guard Cell-to-Leaf Scales – Plant Cell 29: 2921–2935 – DOI: https://doi.org/10.1105/tpc.17.00694 – http://www.plantcell.org/content/29/11/2921?ijkey=615d52f6f112083b64a7d81e76985c6f96eb7ef4&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2018/02/02/66246/ )

Wang Y., Holroyd G., Hetherington A. M., Ng C. K.‐Y. (2004) – Seeing “cool” and ‘hot’—infrared thermography as a tool for non‐invasive, high‐throughput screening of Arabidopsis guard cell signalling mutants – J Exp Bot. 55( 400): 1187‐ 1193 –  https://doi.org/10.1093/jxb/erh135https://academic.oup.com/jxb/article/55/400/1187/528654/ – (On our blog : https://plantstomata.wordpress.com/2019/10/08/the-use-of-infrared-thermography-as-a-non%e2%80%90invasive-high%e2%80%90throughput-tool-and-the-versatility-of-this-technique-for-screening-defective-in-stomatal-regulation/ )

Wang Y., Köhler P., He L., Doughty R., Braghiere R. K., Wood J. D., Frankenberg C. (2021) – Testing stomatal models at stand level in deciduous angiosperm and evergreen gymnosperm forests using CliMA Land (v0.1) – Geosci. Model Dev. Discuss. [preprint] – https://doi.org/10.5194/gmd-2021-154, in review, 2021 – https://gmd.copernicus.org/preprints/gmd-2021-154/ – (On our blog : https://plantstomata.wordpress.com/2021/07/07/using-stomatal-optimization-with-a-comprehensive-rt-model-showed-high-accuracy-in-simulating-land-surface-processes/ )

Wang Y., Liu S., Zhang H., Zhao Y., Zhao H., Liu H. (2014) – Glycine betaine application in grain filling wheat plants alleviates heat and high light-induced photoinhibition by enhancing the psbA transcription and stomatal conductance – Acta Physiologiae Plantarum 36(8): 2195-2202 – http://dx.doi.org/10.1007/s11738-014-1596-7https://link.springer.com/article/10.1007/s11738-014-1596-7 – (On our blog : https://plantstomata.wordpress.com/2020/11/12/gb-accumulation-in-vivo-was-involved-in-the-regulation-of-stomatal-conductance/ )

Wang Y., Ma G., Du X., Liu Y., Wang B., Xu G., Mao H. (2020) – Effects of Nutrient Solution Irrigation Quantity and Downy Mildew Infection on Growth and Physiological Traits of Greenhouse Cucumber – Agronomy 10: 1921 – doi:10.3390/agronomy10121921www.mdpi.com/journal/agronomyfile:///C:/Users/wille/Downloads/agronomy-10-01921.pdf – (On our blog : https://plantstomata.wordpress.com/2022/03/03/leaf-photosynthesis-rate-transpiration-rate-intercellular-co2-concentration-and-stomatal-conductance-were-significantly-decreased-under-b1t2-b1t3-b2t2-and-b2t3-treatments/ )

Wang Y., Noguchi K., Ono N., Inoue S.-i., Terashima I., Kinoshita T. (2014) – Overexpression of plasma membrane H+-ATPase in guard cells promotes light-induced stomatal opening and enhances plant growth – PNAS 111(1): 533-538 – https://doi.org/10.1073/pnas.1305438111 –http://www.pnas.org/content/111/1/533 – (On our blog : https://plantstomata.wordpress.com/2018/11/26/stomatal-aperture-is-a-limiting-factor-in-photosynthesis-and-plant-growth/

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Wilkinson S., Davies W. J. (2008) – Manipulation of the apoplastic pH of intact plants mimics stomatal and growth responses to water availability and microclimatic variation – Journal of Experimental Botany 59: 619– 631 – https://doi.org/10.1093/jxb/erm338https://academic.oup.com/jxb/article/59/3/619/576618 – (On our blog : https://plantstomata.wordpress.com/2019/09/11/manipulation-of-the-apoplastic-ph-of-intact-plants-mimics-stomatal-and-growth-responses/ )

Wilkinson S., Davies W. J. (2009) – Ozone suppresses soil drying- and abscisic acid (ABA)-induced stomatal closure via an ethylene-dependent mechanism – Plant, Cell & Environment 32: 949–959 https://doi.org/10.1111/j.1365-3040.2009.01970.xhttps://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-3040.2009.01970.x – (On our blog : https://plantstomata.wordpress.com/2019/09/11/ozone-suppresses-soil-drying-and-aba-induced-stomatal-closure/ )

Will R. E., Teskey R. O. (1997) – Effect of irradiance and vapour pressure deficit on stomatal responses to CO2 enrichment of four tree species – Journal of Experimental Botany 48: 2095–2102 – https://www.jstor.org/stable/23695484?seq=1 – (On our blog : https://plantstomata.wordpress.com/2021/05/26/stomatal-responses-to-co2-enrichment-2/ )

Wille A. C., Lucas W. J. (1984) – Ultrastructural and histochemical studies on guard cells – Planta 160: 129-142 – https://doi.org/10.1007/BF00392861– https://link.springer.com/article/10.1007/BF00392861#citeas – (On our blog : https://plantstomata.wordpress.com/2018/01/17/ultrastructural-and-histochemical-studies-on-stomata/ )

Willer C. M., Kanai R., Pallas J. E. Jr., Black C. C. Jr. (1973) – Detection of high levels of phosphoenolpyruvate carboxylase in leaf epidermal tissue and its significance in stomatal movements – Life Sci. 12: 151–155 – https://doi.org/10.1016/0024-3205(73)90207-5https://www.sciencedirect.com/science/article/abs/pii/0024320573902075 – (On our blog : https://plantstomata.wordpress.com/2018/11/12/phosphoenolpyruvate-carboxylase-in-leaf-epidermal-tissue-and-its-significance-in-stomatal-movements/ )

Williams A. F. (2013) – Identification of proteins that putatively bind the promoter of the stomatal master regulator gene, MUTE – MSc Thesis Washington University – WWU Graduate School Collection 308 – https://doi.org/10.25710/p944-zy62https://cedar.wwu.edu/wwuet/308/ – (On our blog : https://plantstomata.wordpress.com/2021/12/12/97381/ )

Williams M. (2017)  Autocrine regulation of stomatal differentiation potential by EPF1 and ERECTA-LIKE1 ligand-receptor signaling – March 17, 2017 – in Plant Science Research Weekly – https://plantae.org/autocrine-regulation-of-stomatal-differentiation-potential-by-epf1-and-erecta-like1-ligand-receptor-signaling/ – (On our blog : https://plantstomata.wordpress.com/2022/03/22/a-model-in-which-the-co-presence-of-epf1-erl1-and-mute-inhibits-stomatal-fate-and-epf1-acts-as-an-autocrine-signal/ )

Williams M. (2017) Small Pores with a Big Impact  – https://plantae.org/blog/plant-physiology-focus-issue-on-stomata-published/ – (On our blog : https://plantstomata.wordpress.com/2017/09/18/small-pores-with-a-big-impact/ )

Williams M. (2017) Update: Blue light regulation of stomatal opening and the plasma membrane H+-ATPase – https://plantae.org/update-blue-light-regulation-of-stomatal-opening-and-the-plasma-membrane-h-atpase/?utm_source=TrendMD&utm_medium=cpc&utm_campaign=Plantae_TrendMD_0 – (On our blog : https://plantstomata.wordpress.com/2018/04/14/blue-light-regulation-of-stomatal-opening/ )

Williams M. (2017) – ABA-induced stomatal closure involves ALMT4, a phosphorylation-dependent vacuolar anion channel – in Plant Science – https://plantae.org/blog/aba-induced-stomatal-closure-involves-almt4-a-phosphorylation-dependent-vacuolar-anion-channel/ – (On our blog : https://plantstomata.wordpress.com/2019/11/05/aba-induced-stomatal-closure-involves-almt4/

Williams M. (2020) – Review: Guard cell metabolism and stomatal function (Annu. Rev. Plant Biol.) – June 12, 2020 – in Plant Science Research Weekly – https://plantae.org/review-guard-cell-metabolism-and-stomatal-function-annu-rev-plant-biol/ – (On our blog : https://plantstomata.wordpress.com/2022/03/22/stomatal-guard-cell-metabolism-and-function/ )

Williams M., Rastetter E. B., Fernandes D. N., Goulden M. L.,Wofsy S. C., Shaver G. R., Melillo J. M., Munger J. W., Fan S.-M., Nadelhoffer K. J. (1996) – Modelling the soil-plant-atmosphere continuum in a Quercus- Acer stand at Harvard Forest: the regulation of stomatal conductance by light, nitrogen and soil/plant hydraulic properties – Plant Cell Environ. 19: 911–927 –

Williams W. E., Grivet C., Zeiger E. (1983) – Gas exchange in Paphiopedilum – lack of chloroplasts in guard cells correlates with low stomatal conductance – Plant Physiol 72: 906–908 – https://doi.org/10.1104/pp.72.3.906 – http://www.plantphysiol.org/content/72/3/906.long?utm_source=TrendMD&utm_medium=cpc&utm_campaign=Plant_Physiol_TrendMD_0 – (On our blog : https://plantstomata.wordpress.com/2018/12/11/lack-of-chloroplasts-in-stomata-correlates-with-low-stomatal-conductance/ )

Williams W. T. (1947) – Shock-induced stomatal movements – Nature 160: 364-365 – https://doi.org/10.1038/160364b0https://www.nature.com/articles/160364b0#citeas – (On our blog : https://plantstomata.wordpress.com/2021/12/27/shock-induced-stomatal-movements/ )

Williams W. T. (1949) – Studies in stomatal behaviour. III. The sensitivity of stomata to mechanical shock – Annals of Bot. N. S. 13: 309-329 – https://doi.org/10.1093/oxfordjournals.aob.a083220https://academic.oup.com/aob/article-abstract/13/3/309/207848 – (On our blog : https://plantstomata.wordpress.com/2021/12/23/sensitivity-of-stomata-to-mechanical-shock/ )

Williams W. T. (1950) – Studies in Stomatal Behaviour: IV. THE WATER-RELATIONS OF THE EPIDERMIS – Journal of Experimental Botany 1(1): 114–131 – https://doi.org/10.1093/jxb/1.1.114https://academic.oup.com/jxb/article-abstract/1/1/114/653271?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2021/12/26/the-stomatal-phenomena-and-the-water-relations-of-the-epidermis/ )

Williams W. T. (1952) – Studies in Stomatal Behaviour: II. THE ROLE OF STARCH IN THE LIGHT RESPONSE OF STOMATA – Journal of Experimental Botany 3(1): 110–127 – https://doi.org/10.1093/jxb/3.1.110https://academic.oup.com/jxb/article-abstract/3/1/110/437217 – (On our blog : https://plantstomata.wordpress.com/2021/12/16/the-function-of-carbohydrate-changes-in-stomata-is-the-amplifying-and-stabilizing-of-changes-primarily-controlled-by-other-factors/ )

Williams W. T. (1954) – A new theory of the mechanism of stomatal movement – Jour. Exp. Bot. 5(15): 545-552 – http://www.jstor.org/stable/23686181 – (On our blog : https://plantstomata.wordpress.com/2021/12/16/the-mechanism-of-stomatal-movement-2/ )

Williams W. T., Spencer G. (1950) – Quantitative Estimation of Stomatal Starch – Nature 166: 34–35 – https://doi.org/10.1038/166034b0https://www.nature.com/articles/166034b0#citeas – (On our blog : https://plantstomata.wordpress.com/2021/12/19/quantitative-estimation-of-stomatal-starch/ )

Williams W. T., Shipton M. E. (1950) – Stomatal Behaviour in Buffer Solutions – Physiol. Plant. 3: 479-486 –

Willmer C. M. (1983) – Stomata – London, Longman – 

Willmer C. M. (1983) – Stomatal development and differenciation and the ultrastructure of guard cells. In: Willmer M. (Ed) Stomata (pp 28–50). Longman –

Willmer C. M. (1983) – Phosphoenolpyruvatc carboxylase activity and stomatal operation – Physiologie végétale 21: 943-953 –

Willmer C. M. (1988) – Stomatal sensing of the environment – Biological Journal of the Linnean Society 34: 205-217 – https://doi.org/10.1111/j.1095-8312.1988.tb01959.xhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1095-8312.1988.tb01959.x – (On our blog : https://plantstomata.wordpress.com/2021/05/11/stomatal-sensing-of-the-environment/ )

Willmer C.M. (1993)  The evolution, structure and functioning of stomata – Botanical Journal of Scotland 46(3): 433-445 – https://doi.org/10.1080/03746609308684805 – http://www.tandfonline.com/doi/pdf/10.1080/03746609308684805 – (On our blog : https://plantstomata.wordpress.com/2017/11/30/stomatal-structure-and-functioning/ )

Willmer C. M., Beattle L. N. J. P. (1978) – Cellular osmotic phenomena during stomatal movements of Commelina communisProtoplasma 95(4): 321–332https://doi.org/10.1007/BF01291408https://link.springer.com/article/10.1007/BF01291408#citeas – (On our blog : https://plantstomata.wordpress.com/2019/08/12/cellular-osmotic-phenomena-during-stomatal-movements/ )

Willmer C. M., Dittrich P. (1974) – Carbon dioxide fixation by epidermal and mesophyll tissues of Tulipa and Commelina – Planta 117: 123-132 – doi: 10.1007/BF00390794https://www.ncbi.nlm.nih.gov/pubmed/24458325 – (On our blog : https://plantstomata.wordpress.com/2019/02/27/carbon-dioxide-fixation-by-epidermal-stomata-and-mesophyll-tissues/ )

Willmer C. M., Don R., Parker W. (1978) – Levels of short-chain fatty acids and of abscisic acid in water-stressed and non-stressed leaves and their effects on stomata in epidermal strips and excised leaves – Planta 139: 281–287 – doi: 10.1007/BF00388642 – https://www.ncbi.nlm.nih.gov/pubmed/24414272 – (On our blog : https://plantstomata.wordpress.com/2018/07/17/fatty-acids-aba-and-their-effects-on-stomata-in-epidermal-strips-and-excised-leaves/

Willmer C. M., Fricker M. (1996) – Stomata – In : Topics in Plant Functional Biology: 2 – Eds. M. Black and B. Charlwood – Springer-Science+ Business Media B. V. – https://books.google.be/books?id=9sjoCAAAQBAJ&pg=PA12&lpg=PA12&dq=stomata&source=bl&ots=tIpu1rPm39&sig=YGbF_YtCyNa-YR3F8_QWpf3UugI&hl=en&sa=X&ved=0ahUKEwiS3e-4ocbYAhVMmbQKHcY3DWw4HhDoAQgoMAA#v=onepage&q=stomata&f=false – (On our blog : https://plantstomata.wordpress.com/2018/01/07/stomata-3/ )

Willmer C. M., Fricker M. (1996) – The theory of gas diffusion through stomata – In: Stomata. Springer, Dordrecht – https://doi.org/10.1007/978-94-011-0579-8_5

Willmer C. M., Kanai R., Pallas J. E., Black C. C. (1973) – Detection of high levels of phosphoenolpyruvate carboxylase in leaf epidermal tissue and its significance in stomatal movements – Life Sci. 12: 151-155 –

Willmer C. M., Mansfield T. A. (1969) – A Critical Examination of the Use of Detached Epidermis in Studies of Stomatal Physiology – New Phytol. 68: 363-375 –

Willmer C. M., Mansfield T. A. (1969) – Active cation transport and stomatal opening: possible physiological role of sodium ions – Z. Pflanzenphysiol. 61: 398-400 –

Willmer C. M., Mansfield T. A. (1970) – Further observations of cation-stimulated stomatal opening in isolated epidermis – New Phytol. 69(3): 639-645 – https://doi.org/10.1111/j.1469-8137.1970.tb02451.xhttps://nph.onlinelibrary.wiley.com/doi/abs/10.1111/j.1469-8137.1970.tb02451.x – (On our blog : https://plantstomata.wordpress.com/2019/08/28/active-transport-of-monovalent-cations-into-stomatal-guard-cells-might-explain-the-co2%e2%80%90independent-light-responses-of-stomata-but-not-their-light%e2%80%90independent-co2-responses/ )

Willmer C. M., Mansfield T. A. (1970) – Effects of some metabolic inhibitors and temperature on ion-stimulated stomatal opening in detached epidermis – New Phytol. 69: 983-992 –

Willmer C. M., Pallas J. E. Jr. (1973) – A survey of stomatal movements and associated potassium fluxes in the plant kingdom – Canadian Journal of Botany 51(1): 37-42 – https://doi.org/10.1139/b73-006 – http://www.nrcresearchpress.com/doi/abs/10.1139/b73-006?journalCode=cjb1 – (On our blog : https://plantstomata.wordpress.com/2018/01/28/stomatal-movements-and-associated-potassium-fluxes/ )

Willmer C. M., Pallas J. E. Jr. (1974) – Stomatal movements and ion fluxes within epidermis of Commelina communis L. – Nature (Lond.) 252: 126-l27 – https://doi.org/10.1038/252126a0https://www.nature.com/articles/252126a0#citeas – (On our blog : https://plantstomata.wordpress.com/2021/10/02/stomatal-movements-and-ion-fluxes/ )

Willmer C. M., Pallas J. E., Black C. C. (1973) – Carbon dioxide metabolism in leaf epidermal tissue – Plant Physiol 52: 448-452 –  PMID: 16658581 PMCID: PMC366521 –http://www.plantphysiol.org/content/plantphysiol/52/5/448.full.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/27/carbon-dioxide-metabolism-in-leaf-epidermis-stomata/ )

Willmer C. M., Pantoja O. (1992) – The plasma membrane and tonoplast of guard cells. In: Plant Membranes. Springer, Dordrecht – Plant Membranes : 220-238 – https://link.springer.com/chapter/10.1007/978-94-017-2683-2_11 – (On our blog : https://plantstomata.wordpress.com/2018/09/18/ion-transport-across-the-tonoplast-and-plasma-membrane-play-a-central-role-in-stomatal-functioning/

Willmer C. M., Rutter J. C. (1977) –  Guard Cell Malic Acid Metabolism during Stomtal Movements – Nature 269: 327-328 –

Willmer C. M., Sexton R. (1979)  Stomata and plasmodesmata – Protoplasma 100: 113 – https://doi.org/10.1007/BF01276305 – https://link.springer.com/article/10.1007/BF01276305#citeas – (On our blog : https://plantstomata.wordpress.com/2018/01/07/stomata-and-plasmodesmata/ )

Willmer C. M., Thorpe N., Rutter J. C., Milthorpe F. L. (1978) – Stomatal metabolism: fixation in attached and detached epidermis of Commelina – Aust. J. Plant Physiol. 5: 767–778 – https://doi.org/10.1071/PP9780767http://www.publish.csiro.au/FP/PP9780767 – (On our blog : https://plantstomata.wordpress.com/2019/04/04/stomatal-metabolism-fixation-in-attached-and-detached-epidermis/ )

Willmer C. M., Wilson A. B., Jones H. G. (1988) – Changing responses of
stomata to abscisic acid and CO2 as leaves and plants age – Journal of
Experimental Botany 39: 401–410 – https://doi.org/10.1093/jxb/39.4.401https://academic.oup.com/jxb/article-abstract/39/4/401/438052?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2020/11/18/changing-responses-of-stomata-to-abscisic-acid-and-co2-as-leaves-and-plants-age/ )

Wilson C. C. (1948) – The effect of some environmental factors on the movements of guard cells – Plant Physiol. Lancaster 23: 5-37 –

Wilson D. (1971) – Selection responses of stomatal length and frequency, epidermal ridging, and other leaf characteristics in Lolium perenne l.‘grasslands ruanui’ – New
Zealand Journal of Agricultural Research 14(4): 761-771 – DOI: 10.1080/00288233.1971.10421670https://www.tandfonline.com/doi/pdf/10.1080/00288233.1971.10421670 – (On our blog : https://plantstomata.wordpress.com/2022/02/05/selection-responses-of-stomatal-length-and-frequency-2/ )

Wilson D. (1975) – Leaf growth, stomatal diffusion resistances and photosynthesis during droughting of Lolium perenne populations selected for contrasting stomatal length and frequency – Ann. Applied Biol. – https://doi.org/10.1111/j.1744-7348.1975.tb01523.x – https://onlinelibrary.wiley.com/doi/full/10.1111/j.1744-7348.1975.tb01523.x – (On our blog : https://plantstomata.wordpress.com/2018/03/30/stomatal-diffusion-resistances-and-photosynthesis-during-droughting/ )

Wilson I. D., Ribeiro D. M., Bright J., Confraria A., Harrison J., Barros R. S., Desikan R., Neill S. J., Hancock J. T. (2009) – Role of nitric oxide in regulating stomatal apertures – Plant Signal. Behav. 4: 467-469 – doi: 10.4161/psb.4.5.8545 –https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2676769/ – (On our blog : https://plantstomata.wordpress.com/2019/01/09/a-role-for-no-in-the-fine-tuning-of-the-stomatal-apertures-of-turgid-leaves/ )

Wilson J. A., Ogunkanmi A. B., Mansfield T. A. (1978) – Effects of external potassium supply on stomatal closure induced by abscisic acid – Plant Cell Environ. 1: 199–201 – https://doi.org/10.1111/j.1365-3040.1978.tb00761.x –https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-3040.1978.tb00761.x – (On our blog : https://plantstomata.wordpress.com/2019/04/04/effects-of-external-potassium-supply-on-stomatal-closure-induced-by-aba/ )

Wilson K. B., Baldocchi D. D., Hanson P. J. (2000) – Quantifying stomatal and non-stomatal limitations to carbon assimilation resulting from leaf aging and drought in mature deciduous tree species – Tree Physiology 20: 787–797 – PMID: 12651499 – https://nature.berkeley.edu/biometlab/pdf/wilson_et_al_tree_physiol_2000_vol20_787.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/27/quantifying-stomatal-and-non-stomatal-limitations-to-carbon-assimilation/ )

Wilson K. B., Bunce J. A. (1997) – Effects of carbon dioxide concentration on the interactive effects of temperature and water vapour on stomatal conductance in soybean – Plant, Cell & Environment 20: 230-238 – DOI (10.1046/j.1365-3040.1997.d01-58.x) – https://pubag.nal.usda.gov/catalog/1412253 – (On our blog : https://plantstomata.wordpress.com/2019/02/28/effects-of-co2-concentration-on-the-interactive-effects-of-temperature-and-water-vapour-on-stomatal-conductance/ )

Winkel T., Rambal S. (1990) – Stomatal conductance of some grapevines growing in the field under a Mediterranean environment – Agric. For. Meteorol. 51: 107-121 – https://doi.org/10.1016/0168-1923(90)90010-4https://www.sciencedirect.com/science/article/pii/0168192390900104 – (On our blog : https://plantstomata.wordpress.com/2019/05/13/stomatal-conductance-of-some-grapevines-growing-in-the-field-under-a-mediterranean-environment/ )

Winner W. E. (1980) – Cross-sections of stomata on leaves of Grand fir after heat treatments. Washington. 1980 – https://www.sciencebase.gov/catalog/item/get/51dd9641e4b0f72b4471d317?files.sort=dateUploaded&files.order=desc&files.metadataFirst=false – (On our blog : https://plantstomata.wordpress.com/2021/08/31/cross-sections-of-stomata-on-leaves-of-grand/ )

Winner W. E., Mooney H. A. (1980) – Responses of Hawaiian plants to volcanic sulfur dioxide: stomatal behavior and foliar injury – Science 210(4471): 789–791 – doi:10.1126/science.210.4471.789

Winner W. E., Mooney H. A. (1980) – Ecology of SO2 resistance. II. Photosynthetic changes of shrubs in relation to SO2 absorption and stomatal behavior – Oecologia 44: 296–302 – https://doi.org/10.1007/BF00545231https://link.springer.com/article/10.1007%2FBF00545231#citeas – (On our blog : https://plantstomata.wordpress.com/2021/04/22/the-effects-of-so2-on-photosynthesis-partitioned-between-stomatal-and-nonstomatal-components/ )

Winter K., Schramm M. J. (1986) – Analysis of stomatal and nonstomatal components in the environmental control of CO2 exchange in leaves of Welwitschia mirabilis – Plant Physiol. 82: 173-178 – DOI: https://doi.org/10.1104/pp.82.1.173http://www.plantphysiol.org/content/82/1/173 – (On our blog : https://plantstomata.wordpress.com/2018/11/12/stomatal-and-nonstomatal-components-in-the-environmental-control-of-co2-exchange-in-leaves/ )

Wise R. R. (2016) – Organizational Cell Biology – in Encyclopedia of Cell Biology 2: 324-330 – https://doi.org/10.1016/B978-0-12-394447-4.20030-8https://www.sciencedirect.com/science/article/pii/B9780123944474200308 and https://www.sciencedirect.com/topics/immunology-and-microbiology/plant-stoma – (On our blog : https://plantstomata.wordpress.com/2021/03/02/guard-cell-chloroplasts/ )

Withers C. M., Gay A. P., Mur La. J. (2011) – Are stomatal responses the key to understanding the cost of fungal disease resistance in plants? – Journal of the Science of Food and Agriculture 91: 1538-1540 –

Wittig V. E., Ainsworth E. A., Long S. P. (2007) – To what extent do current and projected increases in surface ozone affect photosynthesis and stomatal conductance of trees? A meta-analytic review of the last 3 decades of experiments – Plant Cell Environ. 30: 1150–1162 – DOI: 10.1111/j.1365-3040.2007.01717.x – https://www.ncbi.nlm.nih.gov/pubmed/17661752 – (On our blog : https://plantstomata.wordpress.com/2019/02/28/effect-of-ozone-on-photosynthesis-and-stomatal-conductance/ )

Witoń D., Sujkowska-Rybkowska M., Dąbrowska-Bronk J., Czarnocka W., Bernacki M., Szechyńska-Hebda M., Karpiński S. (2021) -MITOGEN-ACTIVATED PROTEIN KINASE4 impacts leaf development, temperature, and stomatal movement in hybrid aspen – Plant Physiol. : kiab186 – doi: 10.1093/plphys/kiab186 – Epub ahead of print – PMID: 34010410 – https://pubmed.ncbi.nlm.nih.gov/34010410/ – (On our blog : https://plantstomata.wordpress.com/2021/07/21/the-role-of-mpk4-in-the-genetic-and-environmental-regulation-of-stomatal-formation-differentiation-signaling-and-function/ )

Wohlfahrt G., Brilli F., Hörtnagl L., Xu X., Bingemer H., Hansel A., Loretto F. (2012) – Carbonyl sulfide (COS) as a tracer for canopy photosynthesis, transpiration and stomatal conductance: potential and limitations – Plant, Cell and Environment 35: 657–667 – doi: 10.1111/j.1365-3040.2011.02451.xCarbonyl_sulfide_COS_as_a_tracer_for_can.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/21/cos-as-a-tracer-for-canopy-photosynthesis-transpiration-and-stomatal-conductance/ )

Wolf A., Anderegg W. R. L., Pacala S. W. (2016) – Optimal stomatal behavior with competition for water and risk of hydraulic impairment – PNAS 113 (46) E7222-E7230 – doi:10.1073/pnas.1615144113  –http://www.pnas.org/content/early/2016/10/27/1615144113.short – (On our blog : https://plantstomata.wordpress.com/2016/11/06/optimal-stomatal-behavior/

Wolf T., Guinot D. R., Hedrich R., Dietrich P., Marten I. (2005) – Nucleotides and Mg2+ ions differentially regulate K+ channels and non-selective cation channels present in cells forming the stomatal complex – Plant Cell Physiol. 46(10): 1682-1689 – doi: 10.1093/pcp/pci184 – Epub 2005 Aug 4 – https://pubmed.ncbi.nlm.nih.gov/16081526/ – (On our blog : https://plantstomata.wordpress.com/2021/03/07/the-nucleotide-and-mg2-dependencies-of-time-dependent-kin-and-kout-channels-from-maize-subsidiary-cells-were-examined-showing-that-mgatp-as-well-as-mgadp-function-as-channel-activators/ )

Wolf T., Heidelmann T., Marten I. (2006) – ABA regulation of K(+)-permeable channels in maize subsidiary cells – Plant Cell Physiol. 47(10):1372-1380 – doi: 10.1093/pcp/pcl007 – Epub 2006 Sep 14 – https://pubmed.ncbi.nlm.nih.gov/16973684/ – (On our blog : https://plantstomata.wordpress.com/2021/03/07/the-aba-induced-changes-in-time-dependent-kin-and-kout-currents-from-subsidiary-cells-are-very-similar-to-those-previously-described-for-guard-cells/ )

Wolz K. J., Wertin T. M., Abordo M., Wang D., Leakey A. D. B. (2017) – Diversity in stomatal function is integral to modelling plant carbon and water fluxes – Nature Ecology & Evolution1: 1292–1298 – doi:10.1038/s41559-017-0238-zhttps://www.nature.com/articles/s41559-017-0238-z – (On our blog : https://plantstomata.wordpress.com/2017/11/24/diversity-in-stomatal-function/ )

Wong S. C. (1979) – Stomatal behaviour in relation to photosynthesis – PhD thesis Australian National University – https://www-legacy.dge.carnegiescience.edu/publications/berry/AnnRev2012/1979%20Wong-1.pdf – (On our blog : https://plantstomata.wordpress.com/2021/12/11/97324/ )

Wong S. C., Cowan I. R., Farquhar G. D. (1978) – Leaf Conductance in Relation to Assimilation in Eucalyptus pauciflora Sieb. ex Spreng (Influence of Irradiance and Partial Pressure of Carbon Dioxide) – Plant Physiology 62(4): – https://doi.org/10.1104/pp.62.4.670http://www.plantphysiol.org/content/62/4/670.short – (On our blog : https://plantstomata.wordpress.com/2020/11/30/leaf-conductance-in-relation-to-assimilation/ )

Wong S. C., Cowan I. R., Farquhar G. D. (1979) – Stomatal conductance correlates with photosynthetic capacity – Nature: 282: 424-426 – doi: 10.1038/282424a0https://www.nature.com/articles/282424a0 – (On our blog : https://plantstomata.wordpress.com/2019/02/28/stomatal-conductance-correlates-with-photosynthetic-capacity/ )

Wong S. L., Chen C. W., Huang H. W., Weng J. H. (2012) – Using combined measurements for comparison of light induction of stomatal conductance, electron transport rate and CO2 fixation in woody and fern species adapted to different light regimes – Tree Physiology 32: 535–544 – https://doi.org/10.1093/treephys/tps037 – https://academic.oup.com/treephys/article/32/5/535/1735291 – (On our blog : https://plantstomata.wordpress.com/2019/02/28/combined-measurements-for-comparison-of-light-induction-of-stomatal-conductance-electron-transport-rate-and-co2-fixation/ )

Woo J. G., Kim H. D., Oh B. S. (1991) – Estimation of the ploidy of anther derived Chinese cabbage Brassica campestris ssp. pekinensis by the number of chloroplasts in the guard cells – Res. Rep. Rur. Dev. Adm. 33: 35-39 –

Woo K. B. (1965) Dynamic simulation model of transpiration process with stomatal control mechanism – PhD Thesis Oregon State University – file:///C:/Users/wille/Downloads/WooKwangB1965.pdf – (On our blog : https://plantstomata.wordpress.com/2021/11/20/a-possible-model-of-the-stomatal-control-mechanism-is-proposed/ )

Woo K. B., Stone L. N., Boersma L. (1966) – A conceptual model of stomatal control mechanisms – Wat. Resour. Res. 2(1): 71-84 – DOI: 10.1029/WR002i001p00071https://ui.adsabs.harvard.edu/abs/1966WRR…..2…71W/abstract – (On our blog : https://plantstomata.wordpress.com/2021/11/17/a-conceptual-model-of-the-stomatal-control-mechanism/ )

Woo S. Y. (2010) – Epidermal leaf characteristics and seasonal changes of net photosynthesis of five Populus – African Journal of Biotechnology 9(10): – https://www.ajol.info/index.php/ajb/article/view/78319 – (On our blog : https://plantstomata.wordpress.com/2020/12/08/a-wide-significant-variation-in-the-stomata-size-and-density-of-the-genotypes-of-five-populus/ )

Wood J. G. (1932) – The physiology of xerophytism in Australian plants: The carbohydrate metabolism of plants with tomentose succulent leaves – Immunology & Cell Biology – https://doi.org/10.1038/icb.1932.31https://onlinelibrary.wiley.com/doi/pdf/10.1038/icb.1932.31 – (On our blog : https://plantstomata.wordpress.com/2019/05/13/the-carbohydrate-metabolism-of-plants-with-tomentose-succulent-leaves/ )

Wood J. G. (1934) – The physiology of xerophytism in Australian plants: the stomatal frequencies, transpiration and osmotic pressures of sclerophyll and tomentose-succulent leaved plants – J. Ecol. 22: 69–87 – doi:10.2307/2256096https://www.jstor.org/stable/2256096?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2019/05/13/stomatal-frequencies-transpiration-and-osmotic-pressures-of-sclerophyll-and-tomentose-succulent-leaved-plants/ )

Wood N. T., Allan A. C., Haley A., Viry-Moussaid M., Trewavas A. J. (2000) – The characterization of differential calcium signalling in tobacco guard cells – Plant J 24: 335–344 – https://doi.org/10.1046/j.1365-313x.2000.00881.x – https://onlinelibrary.wiley.com/doi/full/10.1046/j.1365-313x.2000.00881.x – (On our blog :  https://plantstomata.wordpress.com/2019/02/28/differential-calcium-signalling-in-stomatal-guard-cells/ )

Woods D. B., Turner N. C. (1971) – Stomatal response to changing light by four tree species of varying shade tolerance – New Phytol. 70: 77–84 – https://doi.org/10.1111/j.1469-8137.1971.tb02512.x – https://nph.onlinelibrary.wiley.com/doi/full/10.1111/j.1469-8137.1971.tb02512.x – (On our blog : https://plantstomata.wordpress.com/2018/07/19/stomatal-response-to-changing-light/ )

Woodruff D. R., Mcculloh K. A., Warren J. M., Meinzer F. C., Lachenbruch B. (2007) – Impacts of tree height on leaf hydraulic architecture and stomatal control in Douglas-fir – Plant Cell Environ. 30: 559–569 – https://doi.org/10.1111/j.1365-3040.2007.01652.xhttps://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-3040.2007.01652.x – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/88613)

Woodruff D., Meinzer F. C., McCulloh K. A. (2009) – Height-related trends in stomatal sensitivity to leaf-to-air vapour pressure deficit in a tall conifer – Journal of Experimental Botany 61(1): 203-210 –https://www.ncbi.nlm.nih.gov/pubmed/19933710 – (On our blog : https://plantstomata.wordpress.com/2016/11/06/stomatal-sensitivity-to-leaf-to-air-vapour-pressure-deficit/ )

Woodward A. W., Bartel B. (2018) – Biology in Bloom: A Primer on the Arabidopsis thaliana Model System – GENETICS 208(4): 1337-1349 – https://doi.org/10.1534/genetics.118.300755http://www.genetics.org/content/208/4/1337 – (On our blog : https://plantstomata.wordpress.com/2019/02/08/arabidopsis-thaliana-model-system/ )

Woodward F. I. (1987)  Stomatal numbers are sensitive to increases in CO2 from pre-industrial levels – Nature 327: 617–618 – doi:10.1038/327617a0https://www.nature.com/nature/journal/v327/n6123/abs/327617a0.html – (On our blog : https://plantstomata.wordpress.com/2017/07/23/increases-in-co2-from-pre-industrial-levels-and-stomatal-density/ )

Woodward F. I. (1998) – Do plants really need stomata? – Journal of Experimental Botany 49: 471-480 – http://www.esalq.usp.br/lepse/imgs/conteudo_thumb/Do-plants-really-need-stomata.pdf – (On our blog : https://plantstomata.wordpress.com/2017/10/26/do-plants-really-need-stomata/ )

Woodward F. I. (2012) – Stomata – a global view  – Presentation at New Phytologist Symposium Nr. 29 on Stomata 2012 –https://www.newphytologist.org/app/webroot/img/upload/files/29thNPSAbstractBook.pdf – (On our blog : https://plantstomata.wordpress.com/2018/01/13/a-global-view-on-stomata/ )

Woodward F. I., Bazzaz F. A. (1987) – The responses of stomatal density to CO2 partial-pressure – Journal of Experimental Botany 39: 1771–1781 – https://doi.org/10.1093/jxb/39.12.1771 – https://academic.oup.com/jxb/article-abstract/39/12/1771/542607 – (On our blog : https://plantstomata.wordpress.com/2019/02/28/stomatal-density-and-co2-partial-pressure/ )

Woodward F. I., Kelly C. K. (1995) – The influence of CO2 concentration on stomatal density – New Phytologist 131: 311-327 – http://onlinelibrary.wiley.com/store/10.1111/j.1469-8137.1995.tb03067.x/asset/j.1469-8137.1995.tb03067.x.pdf?v=1&t=jd6h95wl&s=df4433366e7bdeb84775b67a8c73c5d4c03837ca – (On our blog : https://plantstomata.wordpress.com/2018/02/02/co2-concentration-and-stomatal-density-2/ )

Woodward F. I., Lake C. K., Quick W. P. (2002) – Stomatal development and CO2:  ecological consequences – New Phytologist 153: 477-484 – https://doi.org/10.1046/j.0028-646X.2001.00338.x – https://nph.onlinelibrary.wiley.com/doi/abs/10.1046/j.0028-646X.2001.00338.x – (On our blog : https://plantstomata.wordpress.com/2018/10/13/stomatal-development-and-co2-ecological-consequences/ )

Woolfenden H. C., Baillie A. L., Gray J. E., Hobbs J. K., Morris R. J., Fleming A. J. (2018) – Models and Mechanisms of Stomatal Mechanics –  In Press Corrected Proof – Trends in Plant Science – https://doi.org/10.1016/j.tplants.2018.06.003 – https://www.cell.com/trends/plant-science/fulltext/S1360-1385(18)30132-8 – (On our blog : https://plantstomata.wordpress.com/2018/07/13/a-reassessment-of-accepted-paradigms-and-a-new-understanding-of-the-mechanism-of-stomatal-mechanics/ )

Woolfenden H. C., Bourdais G., Kopischke M., Miedes E., Molina A., Robatzek S., Morris R. J. (2017)  A computational approach for inferring the cell wall properties that govern guard cell dynamics – The Plant Journal – DOI: 10.1111/tpj.13640 – http://onlinelibrary.wiley.com/doi/10.1111/tpj.13640/abstract – (On our blog : https://plantstomata.wordpress.com/2017/07/29/proper-stomatal-dynamics-builds-on-two-key-properties-of-the-cell-wall-namely-anisotropy-in-the-form-of-hoop-reinforcement-and-strain-stiffening/ )

Wong S. C., Canny M. J., Holloway-Phillips M., Stuart-Williams H., Cernusak L. A., Márquez D. A., Farquhar G. D. (2022) – Humidity gradients in the air spaces of leaves – Nat. Plants 8: 971–978 – https://doi.org/10.1038/s41477-022-01202-1https://www.nature.com/articles/s41477-022-01202-1 – (On our blog : https://plantstomata.wordpress.com/2022/08/19/humidity-gradients-in-the-air-spaces-of-leaves/ )

Wright L. A., Murphy T. M. (1982) – Short-wave ultraviolet light closes leaf stomata – Am J Bot 69: 1196–1199 – https://doi.org/10.1002/j.1537-2197.1982.tb13364.xhttps://bsapubs.onlinelibrary.wiley.com/doi/abs/10.1002/j.1537-2197.1982.tb13364.x – (On our blog : https://plantstomata.wordpress.com/2019/06/27/closing-of-stomata-may-account-for-the-acceleration-of-senescence-that-is-induced-by-ultraviolet-light/ )

Wu B., Long J. Ci (2001) – Landscape change and desertification development in the Mu Us Sandland, Northern China – J. Arid Environ. 50: 429-444 – DOI: 10.1006/jare.2001.0847

Wu B. J., Liu Y. J., Jiang C. D., Shi L. (2015) – Effects of stomatal development on leaf temperature during leaf expansion – Plant Physiology Journal 51: 119-126 –


[ 吴冰洁, 刘玉军, 姜闯道, 石雷 (2015). 叶片生长进程中气孔发育对叶温调节的影响. 植物生理学报, 51,119-126.]

Wu B.-J., Chow W. S., Liu Y.-J., Shi L., Jiang C.-D. ( 2014) – Effects of stomatal development on stomatal conductance and on stomatal limitation of photosynthesis in Syringa oblata and Euonymus japonicus Thunb – Plant Science 229: 23–31 – Effects_of_stomatal_development_on_stoma.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/19/effects-of-stomatal-development-on-stomatal-conductance-and-on-stomatal-limitation-of-photosynthesis/ )

Wu F., Chi Y., Jiang Z. et al. (2020) – Hydrogen peroxide sensor HPCA1 is an LRR receptor kinase in Arabidopsis – Nature (2020) – https://doi.org/10.1038/s41586-020-2032-3 https://www.nature.com/articles/s41586-020-2032-3#citeas – (On our blog : https://plantstomata.wordpress.com/2020/02/20/hpca1-mediates-h2o2-induced-activation-of-ca2-channels-in-guard-cells-and-is-required-for-stomatal-closure/ )

Wu G., Jia H., Huang Y., Gan L., Fu C., Zhang L., Yu L., Li M. (2014) – Characterization and Molecular Interpretation of the Photosynthetic Traits of Lonicera confusa in Karst Environment – PLoS ONE 9(6): e100703 – https://doi.org/10.1371/journal.pone.0100703https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0100703 – (On our blog : https://plantstomata.wordpress.com/2022/09/18/transpiration-stomata-conductance-and-photosynthetic-traits-of-lonicera-confusa-in-karst-environment/ )

Wu G., Liu H., Hua L., Luo Q., Lin Y., He P., Feng S., Liu J., Ye Q. (2018) – Differential Responses of Stomata and Photosynthesis to Elevated Temperature in Two Co-occurring Subtropical Forest Tree Species – Front. Plant Sci. 9: 467-479 – https://doi.org/10.3389/fpls.2018.00467 – https://www.frontiersin.org/articles/10.3389/fpls.2018.00467/full – (On our blog : https://plantstomata.wordpress.com/2018/10/13/two-tree-species-responded-differently-to-water-deficit-caused-by-elevated-temperature-through-the-adjustment-of-stomata/ )

Wu H.-C, Huang Y.-C., Stracovsky L., Jinn T.-L. (2017)  Pectin methylesterase is required for guard cell function in response to heat – Plant Signaling & Behavior  12(6) – http://dx.doi.org/10.1080/15592324.2017.1338227 http://www.tandfonline.com/doi/full/10.1080/15592324.2017.1338227?src=recsys – (On our blog : https://plantstomata.wordpress.com/2017/10/28/the-significant-role-of-pme34-in-heat-tolerance-through-the-regulation-of-stomatal-movement/ )

Wu H.-i., Sharpe P. J. H. (1979) – Stomatal mechanics – II: Material properties of guard cell walls – Plant, Cell and Environment 2: 235-244 –  DOI: 10.1111/j.1365-3040.1979.tb00075.xhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-3040.1979.tb00075.x – (On our blog : https://plantstomata.wordpress.com/2019/02/28/material-properties-of-stomatal-guard-cell-walls/ )

Wu H.-i, Sharpe P. J. H., Spence R. D. (1985) – Stomatal mechanics. III. Geometric interpretation of the mechanical advantage – Plant, Cell & Environment 8: 269–274 – https://doi.org/10.1111/1365-3040.ep11604674 – https://onlinelibrary.wiley.com/doi/abs/10.1111/1365-3040.ep11604674 – (On our blog : https://plantstomata.wordpress.com/2019/02/28/simple-geometric-relationships-calculated-from-measurable-anatomical-dimensions-of-the-stomatal-system/ )

Wu J., Serbin S. P., Ely K. S., Wolfe B. T., Dickman L. T., Grossiord C., Michaletz S. T., Collins A. D., Detto M., McDowell N. G., Wright S. J., Rogers A. (2019) – The response of stomatal conductance to seasonal drought in tropical forests – Global Change Biology – https://doi.org/10.1111/gcb.14820https://onlinelibrary.wiley.com/doi/abs/10.1111/gcb.14820 – (On our blog : https://plantstomata.wordpress.com/2022/05/14/response-of-stomatal-conductance-to-seasonal-drought/ )

Wu L., Huang Z., Li X.,  Ma L., Gu Q..Wu H., Liu J., Borriss R., Wu Z., Gao X., (2018) – Stomatal Closure and SA-, JA/ET-Signaling Pathways Are Essential for Bacillus amyloliquefaciens FZB42 to Restrict Leaf Disease Caused by Phytophthora nicotianae in Nicotiana benthamiana – Front. Microbiol. 27 April 2018 – https://doi.org/10.3389/fmicb.2018.00847 – https://www.frontiersin.org/articles/10.3389/fmicb.2018.00847/full – (On our blog : https://plantstomata.wordpress.com/2018/09/19/stomatal-movements-and-a-biocontrol-mechanism-of-soil-rhizobacteria-in-a-plant/ )

Wu S., Maseyk K., Lett C., Seibt U. (2018 ?) – Stomatal control of leaf fluxes of carbonyl sulfide and CO2 in a Typha freshwater marsh – Biogeosciences Discuss. – https://doi.org/10.5194/bg-2017-431, in review, 2017 – https://www.biogeosciences-discuss.net/bg-2017-431/ – (On our blog : https://plantstomata.wordpress.com/2018/01/07/stomatal-control-of-leaf-fluxes-of-cos-and-co2/ )

Wu T.-C., Lin B.-L., Kao W.-Y. (2020) – Active stomatal control of Marsilea crenata in response to CO2 concentration and exogenous application of ABA – Taiwania 65(4): 431–437 – DOI: 10.6165/tai.2020.65.431https://taiwania.ntu.edu.tw/pdf/tai.2020.65.431.pdf – (On our blog : https://plantstomata.wordpress.com/2021/04/16/active-stomatal-control-in-response-to-co2-concentration-and-exogenous-application-of-aba/ )

Wu T.-C., Lin B.-L., Kao W.-Y. (2020) – Stomatal blue light response is present in Marsilea crenata, an amphibious fern – Taiwania 65(4): 456-462 – DOI: 10.6165/tai.2020.65.456https://taiwania.ntu.edu.tw/abstract.php?type=referance&id=1709 – (On our blog : https://plantstomata.wordpress.com/2021/01/24/stomatal-bl-specific-response-in-a-fern/ )

Wu W. H., Assmann S. M. (1993) – Photosynthesis by guard cell chloroplasts of Vicia faba L. : effects of factors associated with stomatal movement – Plant Cell Physiology 34: 1015-1022 – https://doi.org/10.1093/oxfordjournals.pcp.a078514 –https://academic.oup.com/pcp/article-abstract/34/7/1015/1810682?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2019/03/01/photosynthesis-by-guard-cell-chloroplasts-effects-of-factors-associated-with-stomatal-movement/ )

Wu W. H., Assmann S. M. (1994) – A membrane-delimited pathway of G protein regulation of the guard-cell inward K+channel – Proc Natl Acad Sci USA 91: 6310–6314 – https://doi.org/10.1073/pnas.91.14.6310 – http://www.pnas.org/content/91/14/6310?ijkey=0c9c7541994d9f3dd37d34ba334875c55d199d9e&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2018/09/05/g-proteins-can-act-via-a-membrane-delimited-pathway-to-regulate-inward-k-channels-in-stomata/ )

Wu W. H., Assmann S. M. (1995) – Is ATP required for K+ channel activation in Vicia guard cells? – Plant Physiol. 107: 101–109 – https://doi.org/10.1104/pp.107.1.101http://www.plantphysiol.org/content/107/1/101 – (On our blog : https://plantstomata.wordpress.com/2019/03/01/atp-is-required-for-activation-of-the-inward-k-channels-of-the-stomatal-guard-cell-plasma-membrane/ )

Wu X., Qiao Z., Liu H., Acharya B. R., Li C., Zhang W. (2017) – CML20, an Arabidopsis Calmodulin-like Protein, Negatively Regulates Guard Cell ABA Signaling and Drought Stress Tolerance – Front Plant Sci. 8: 824-824 – doi:10.3389/fpls.2017.00824

Wu X., Sun T., Xu W., Sun Y., Wang B., Wang Y., Li Y., Wang J., Wu X., Lu Z., Xu P., Li G. (2021) – Unraveling the Genetic Architecture of Two Complex, Stomata-Related Drought-Responsive Traits by High-Throughput Physiological Phenotyping and GWAS in Cowpea (Vigna. unguiculata L. Walp) – Front. Genet., 28 October 2021 – https://doi.org/10.3389/fgene.2021.743758https://www.frontiersin.org/articles/10.3389/fgene.2021.743758/full – (On our blog : https://plantstomata.wordpress.com/2022/02/01/forward-genetic-mapping-of-the-genetic-architecture-of-stomatal-traits-related-to-drought-tolerance/ )

Wu X., Xu Y., Shi J., Zuo Q., Zhang T., Wang L., Xue X., Ben-Gal A. (2021) – Estimating stomatal conductance and evapotranspiration of winter wheat using a soil-plant water relations-based stress index -Agricultural and Forest Meteorology 303: 108393 – ISSN 0168-1923 –
https://doi.org/10.1016/j.agrformet.2021.108393
https://www.sciencedirect.com/science/article/pii/S0168192321000769 – (On our blog : https://plantstomata.wordpress.com/2022/04/20/a-novel-soil-water-stress-index-%cf%89-should-be-feasible-and-reliable-to-delineate-the-response-of-stomatal-physiological-reaction-to-water-stress/ )

Wu Y. P., Hu X. W., Wang Y. R. (2009) – Growth, water relations, and stomatal development of Caragana korshinskii Kom. and Zygophyllum xanthoxylum (Bunge) Maxim. seedlings in response to water deficits – New Zealand Journal of Agricultural Research 52(2): 185-193 – DOI: 10.1080/00288230909510503https://www.tandfonline.com/doi/pdf/10.1080/00288230909510503 – (On our blog : https://plantstomata.wordpress.com/2021/12/23/stomatal-development-under-three-watering-regimes/ )

Wu Z., Chen L., Yu Q., Zhou W., Gou X., Li J., Hou S. (2019) – Multiple transcriptional factors control stomata development in rice – New Phytologist – https://doi.org/10.1111/nph.15766 –https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.15766?af=R – (On our blog : https://plantstomata.wordpress.com/2019/03/03/how-various-species-reprogramme-the-molecular-mechanisms-to-generate-different-stomatal-types-during-evolution/ )

Wullschleger S. D., Gunderson C. A., Hanson P. J., Wilson K. B., Norby R. J. (2002) – Sensitivity of stomatal and canopy conductance to elevated CO2 concentration – interacting variables and perspectives of scale – New Phytologist 153: 485–496 – https://doi.org/10.1046/j.0028-646X.2001.00333.x –https://nph.onlinelibrary.wiley.com/doi/10.1046/j.0028-646X.2001.00333.x – (On our blog : https://plantstomata.wordpress.com/2019/03/01/sensitivity-of-stomatal-and-canopy-conductance-to-elevated-co2-concentration/ )

Wullschleger S. D., Hanson P. J., Sage R. F. (1992) – PHOTOBIO: Modeling the Stomatal and Biochemical Control of Plant Gas Exchange -J. Nat. Resour. Life Sci. Educ. 21: 141-145 – https://www.crops.org/files/publications/nse/pdfs/jnr021/021-02-0141.pdf – (On our blog : https://plantstomata.wordpress.com/2018/09/23/modeling-the-stomatal-and-biochemical-control-of-plant-gas-exchange/ )

Wullschleger S. D., Oosterhuis D. M. (1989) – The occurrence of an internal cuticle in cotton (Gossypium hirsutum L.) leaf stomates -Environmental and Experimental Botany 29: 229– 235 –

Würzburg University (Germany) – Department of Botany I – Plant Physiology and Biophysics (xxxx) – Prof. R. Hedrich – Stomatal movement – guard cell physiology – http://www.bot1.biozentrum.uni-wuerzburg.de/en/research/prof-dr-rainer-hedrich/stomata-guard-cell-action/ – (On our blog : https://plantstomata.wordpress.com/2018/01/17/stomatal-movements/ )

Würzburg University (Germany) – Department of Botany I – Plant Physiology and Biophysics (xxxx) – Prof. R. Hedrich – ABA action and receptors – http://www.bot1.biozentrum.uni-wuerzburg.de/en/research/prof-dr-rainer-hedrich/stomata-guard-cell-action/ – (On our blog : https://plantstomata.wordpress.com/2018/01/17/aba-action-and-receptors-in-stomata/ )

Würzburg University (Germany) – How Plants React to Fungi – 10/07/2019 – https://www.uni-wuerzburg.de/en/news-and-events/news/detail/news/how-plants-react-to-fungi/ – (On our blog : https://plantstomata.wordpress.com/2019/12/03/how-the-plant-recognizes-fungi-and-the-molecular-signalling-chain-via-which-the-chitin-triggers-the-closure-of-the-stomata/ )

Wyka T. P., Duarte H. M., Lüttge U. E. (2005) – Redundancy of stomatal control for the circadian photosynthetic rhythm in Kalanchoë daigremontiana Hamet et Perrier – Plant Biol (Stuttg) 7(2): 176-181 – doi: 10.1055/s-2005-837541https://pubmed.ncbi.nlm.nih.gov/15822013/ – (On our blog : https://plantstomata.wordpress.com/2022/03/08/photosynthetic-rhythmicity-is-independent-of-stomatal-regulation-and-may-originate-in-the-mesophyll/ )

Wynn J. G. (2003)  Towards a physically based model of CO2-induced stomatal frequency response – New Phytol. 157: 394–398 –Towards_a_physically_based_model_of_CO2-.pdf – (On our blog : https://plantstomata.wordpress.com/2017/12/12/a-physically-based-model-of-co2-induced-stomatal-frequency-response/ )

Wynn W. (1976) – Appressorium formation over stomata by the bean rust fungus: response to a surface contact stimulus – Phytopathology 66: 136–146 – DOI: 10.1094/Phyto-66-136https://www.apsnet.org/publications/phytopathology/backissues/Documents/1976Abstracts/Phyto66_136.htm – (On our blog : https://plantstomata.wordpress.com/2021/04/02/the-specific-surface-feature-which-induced-appressorium-formation-on-leaves-was-apparently-the-stomatal-lips/ )

Xia X. J., Gao C. J., Song L. X., Zhou Y. H., Shi K., Yu J. Q. (2014) – Role of H2O2 dynamics in brassinosteroid-induced stomatal closure and opening in Solanum lycopersicum – Plant Cell Environ. 37: 2036–2050 – doi: 10.1111/pce.12275 – https://www.ncbi.nlm.nih.gov/pubmed/24428600 – (On our blog : https://plantstomata.wordpress.com/2018/07/20/aba-deficiency-abolished-ebr-induced-stomatal-closure-but-did-not-affect-ebr-induced-stomatal-opening/

Xia Z. H., Chen Y. N., Zhu C. G., Zhou Y. Y., Chen X. L. (2018) – Stomatal change in leaves of population euphratica under drought stress – Arid Zone Research 35: 1111-1117 –


[ 夏振华, 陈亚宁, 朱成刚, 周莹莹, 陈晓林 (2018). 干旱胁迫环境下的胡杨叶片气孔变化. 干旱区研究, 35,1111-1117.]

Xiang Q., Lott A. A., Assmann S. M., Chen S. (2021) – Advances and perspectives in the metabolomics of stomatal movement and the disease triangle – Plant Science 302 – https://doi.org/10.1016/j.plantsci.2020.110697https://www.sciencedirect.com/science/article/abs/pii/S0168945220303034?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2021/12/02/recent-advances-toward-understanding-the-stomatal-disease-triangle-in-the-context-of-newly-discovered-signaling-molecules/ )

Xiao C., Guo H., Tang J., Li J., Yao X. (2021) – Expression Pattern and Functional Analyses of Arabidopsis Guard Cell-Enriched GDSL Lipases – Frontiers in Plant Science 12 – DOI: 10.3389/fpls.2021.748543https://www.researchgate.net/publication/354731386_Expression_Pattern_and_Functional_Analyses_of_Arabidopsis_Guard_Cell-Enriched_GDSL_Lipases – (On our blog : https://plantstomata.wordpress.com/2021/09/27/functional-insights-into-the-ggls-to-control-stomatal-dynamics-and-development-plant-growth-and-adaptation-to-the-environment/ )

Xie C., Zhang R., Qu Y., Miao Z., Zhang Y., Shen X., Wang T, Dong J. (2012) – Overexpression of MtCAS31 enhances drought tolerance in transgenic Arabidopsis by reducing stomatal density – New Phytol. 19: 5124–135 – DOI:  10.1111/j.1469-8137.2012.04136.x – https://www.ncbi.nlm.nih.gov/pubmed/22510066 – (On our blog : https://plantstomata.wordpress.com/2019/03/01/interaction-of-mtcas31-and-atice1-caused-the-decrease-in-stomatal-density/ )

Xie K. (2019) – Food for the Future: How Artificial Intelligence Can Improve Drought Resistance – FFAR Dec. 19, 2019 – https://foundationfar.org/2019/12/19/food-for-the-future-how-artificial-intelligence-can-improve-drought-resistance/ – (On our blog : https://plantstomata.wordpress.com/2020/04/22/can-we-find-a-good-balance-point-where-plants-capture-the-most-co2-possible-while-using-the-least-possible-amount-of-water/ )

Xie R., Zhao J., Lu L., Brown P., Guo J., Tian S. (2020) – Penetration of foliar-applied Zn and its impact on apple plant nutrition status: in vivo evaluation by synchrotron-based X-ray fluorescence microscopy – Hortic Res 7, Art.147 – https://doi.org/10.1038/s41438-020-00369-yhttps://www.nature.com/articles/s41438-020-00369-y#Sec15 – (On our blog : https://plantstomata.wordpress.com/2021/01/22/direct-visual-evidence-for-the-zn-penetration-process-across-the-leaf-surface/ )

Xie S., Luo X. (2003) – Effect of leaf position and age on anatomical structure, photosynthesis, stomatal conductance and transpiration of Asian pear – Bot. Bull. Acad. Sin. 44: 297-303 – https://ejournal.sinica.edu.tw/bbas/content/2003/4/bot444-06.html – (On our blog : https://plantstomata.wordpress.com/2018/01/13/leaf-position-and-age-stomatal-conductance-and-transpiration-of-asian-pear/ )

Xie X., Mayfield-Jones D., Erice G., Choi M., Leakey A. D. B. (2020) – Optical topometry and machine learning to rapidly phenotype stomatal patterning traits for QTL mapping in maize – BioRXiv – https://doi.org/10.1101/2020.10.09.333880https://www.biorxiv.org/content/10.1101/2020.10.09.333880v1 – (On our blog : https://plantstomata.wordpress.com/2021/05/01/how-discovery-of-the-genetic-basis-for-stomatal-patterning-can-be-accelerated-in-maize/ )

Xie X., Wang Y., Williamson L., Holroyd G. H., Tagliavia C., Murchie E., Theobald J., Knight M. R., Davies W. J., Leyser H. M. O., Hetherington A. M. (2006) – The identification of genes involved in the stomatal response to reduced atmospheric relative humidity. – Curr. Biol. 16: 882–887 – https://doi.org/10.1016/j.cub.2006.03.028 – http://www.cell.com/current-biology/fulltext/S0960-9822(06)01324-8?_returnURL=http%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0960982206013248%3Fshowall%3Dtrue – (On our blog : https://plantstomata.wordpress.com/2018/02/02/genes-for-the-stomatal-response-to-reduced-atmospheric-relative-humidity/ )

Xie Y., Mao Y., Duan X., Zhou H., Lai D., Zhang Y., Shen W. (2016) – Arabidopsis HY1-Modulated Stomatal Movement: An Integrative Hub Is Functionally Associated with ABI4 in Dehydration-Induced ABA Responsiveness – Plant Physiology 170(3):  –https://doi.org/10.1104/pp.15.01550 –http://www.plantphysiol.org/content/170/3/1699 – (On our blog : https://plantstomata.wordpress.com/2017/11/06/hy1-modulated-stomatal-movement/ )

Xie Y., Mao Y., Zhang W., Lai D., Wang Q., Shen W. (2014) – Reactive oxygen species-dependent nitric oxide production contributes to hydrogen- promoted stomatal closure in Arabidopsis – Plant Physiol. 165: 759–773 – doi: 10.1104/pp.114.237925 – http://www.plantphysiol.org/content/early/2014/04/14/pp.114.237925 – (On our blog : https://plantstomata.wordpress.com/2018/07/20/no-production-contributes-to-h2-promoted-stomatal-closure/ )

Xie Z., Lee E., Lucas J. R., Morohashi K., Li D., Murray J. A., Sack F. D., Grotewold E. (2010) – Regulation of cell proliferation in the stomatal lineage by the Arabidopsis MYB FOUR LIPS via direct targeting of core cell cycle genes – The Plant Cell 22: 2306–2321 –  https://doi.org/10.1105/tpc.110.074609http://www.plantcell.org/content/22/7/2306 – (On our blog : https://plantstomata.wordpress.com/2019/05/03/regulation-of-cell-proliferation-in-the-stomatal-lineage-by-myb-four-lips-via-direct-targeting-of-core-cell-cycle-genes/ )

Xie Z., Li D., Wang L., Sack F. D., Grotewold E. (2010) – Role of the stomatal development regulators FLP/MYB88 in abiotic stress responses – The Plant Journal 64(5): 731-739 – https://doi.org/10.1111/j.1365-313X.2010.04364.xhttps://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-313X.2010.04364.x – (On our blog : https://plantstomata.wordpress.com/2021/05/02/the-stomatal-development-regulators-flp-myb88/ )

Xinhua (2017) – Grass stomata seen as possible lead to crops better surviving climate change – http://news.xinhuanet.com/english/2017 – 03/17/c_136135449.htm – (On our blog : https://plantstomata.wordpress.com/2017/10/30/these-findings-may-lead-to-producing-other-plants-with-four-celled-stomata/ )

Xiong D., Douthe C., Flexas J. (2018) Differential coordination of stomatal conductance, mesophyll conductance and leaf hydraulic conductance in response to changing light across species – Plant Cell Environ. 41: 821-827 – https://doi.org/10.1111/pce.13111http://onlinelibrary.wiley.com/doi/10.1111/pce.13111/abstract – (On our blog : https://plantstomata.wordpress.com/2017/12/10/differential-coordination-of-stomatal-conductance/ )

Xiong D., Flexas J. (2020) – From one side to two sides: the effects of stomatal distribution on photosynthesis – New Phytologist 228(6): 1754-1766 –  doi: 10.1111/nph.16801 – Epub 2020 Aug 28 – https://pubmed.ncbi.nlm.nih.gov/32652573/ – (On our blog : https://plantstomata.wordpress.com/2021/01/25/the-shift-of-stomatal-pores-from-one-leaf-side-to-both-sides-played-an-important-role-in-regulating-co2-diffusion-via-both-stomata-and-mesophyll-tissues/ )

Xiong D., Flexas J., Peng S., Huang J. (2017) – Leaf anatomy mediates coordination of leaf hydraulic conductance and mesophyll conductance to CO2 in Oryza – New Phytol. 213(2): 572-583 – doi: 10.1111/nph.14186 – Epub 2016 Sep 2 – https://www.ncbi.nlm.nih.gov/pubmed/27653809 – (On our blog : https://plantstomata.wordpress.com/2019/08/30/kleaf-was-not-correlated-with-the-maximum-theoretical-stomatal-conductance/ )

Xiong H., Ma C. E., Li L., Zeng H., Guo D. L. (2014) – Stomatal characteristics of ferns and angiosperms and their responses to changing light intensity at different habitats – Chinese Journal of Plant Ecology 38: 868-877 -[ 熊慧, 马承恩, 李乐, 曾辉, 郭大立 (2014). 不同生境条件下蕨类和被子植物的气孔形态特征及其对光强变化的响应. 植物生态学报, 38,868-877.]

Xiong Z., Xiong D., Cai D., Wang W., Cui K., Peng J., Huang J. (2021) – Effect of stomatal morphology on leaf photosynthetic induction under fluctuating light across diploid and tetraploid rice – Environmental and Experimental Botany 194(12): 104757 – DOI: 10.1016/j.envexpbot.2021.104757https://www.researchgate.net/publication/357107150_Effect_of_stomatal_morphology_on_leaf_photosynthetic_induction_under_fluctuating_light_across_diploid_and_tetraploid_rice – (On our blog : https://plantstomata.wordpress.com/2022/04/22/the-function-of-stomata-in-regulating-photosynthetic-induction-and-water-use-efficiency-under-fluctuating-light/ )

Xu B., Long Y., Feng X., Zhu X., Sai N., Chirkova L., Betts A., Herrmann J., Edwards E. J., Okamoto M., Hedrich R., Gilliham M. (2021) – GABA signalling modulates stomatal opening to enhance plant water use efficiency and drought resilience – Nat Commun 12: 1952 – https://doi.org/10.1038/s41467-021-21694-3 – https://www.nature.com/articles/s41467-021-21694-3 – (On our blog : https://plantstomata.wordpress.com/2021/07/04/gaba-signalling-modulates-stomatal-opening/ )

Xu B.-s., Zhang R.-h. ( 2002) – Study on chlorophyll content and stomata morphology of Pïnus massoniana – Chemistry and Industry of Forest Products 22(3): 59-61  – http://www.cifp.ac.cn/EN/abstract/abstract94.shtml – (On our blog : https://plantstomata.wordpress.com/2018/02/06/stomata-density-is-negatively-correlated-with-stomata-diameter-in-pinus/ )

Xu D. Q., Terashima K., Crang R. F. E., Chen X. M., Hesketh J. D. (1994) – Stomatal and nonstomatal acclimation to a CO2 enriched atmosphere – Biotronics 23: 1–9 –

Xu H.-L., Gauthier L., Gosselin A. (1995) – Stomatal and Cuticular Transpiration of Greenhouse Tomato Plants in Response to High Solution Electrical Conductivity and Low Soil Water Content – J. AMER. SOC. HORT. SCI. 120(3): 417-422 – file:///C:/Users/wille/Downloads/[23279788%20-%20Journal%20of%20the%20American%20Society%20for%20Horticultural%20Science]%20Stomatal%20and%20Cuticular%20Transpiration%20of%20Greenhouse%20Tomato%20Plants%20in%20Response%20to%20High%20Solution%20Electrical%20Conductivity%20and%20Low%20Soil%20Water%20Co%20(1).pdf – (On our blog : https://plantstomata.wordpress.com/2021/04/01/stomatal-and-cuticular-transpiration-of-greenhouse-tomato-plants/ )

Xu J., Zheng Y., He Y., Zhu F., Mai B., Wang S., Zhang M., Zhao X., Wang L., Xu L., Ding L., Guo Z. (2019) – Estimating stomatal conductance and partitioning total ozone uptake over a winter wheat field – Atmospheric Pollution Research 10(3): 904-912 – https://doi.org/10.1016/j.apr.2018.12.018https://www.sciencedirect.com/science/article/abs/pii/S1309104218305099 – (On our blog : https://plantstomata.wordpress.com/2022/04/17/estimating-stomatal-conductance-and-partitioning-total-ozone-uptake/ )

Xu K., Guo L., Ye H. (2019) – A naturally optimized mass transfer process: The stomatal transpiration of plant leaves – J Plant Physiol. 234-235: 138-144 – doi: 10.1016/j.jplph.2019.02.004https://www.ncbi.nlm.nih.gov/pubmed/30798115 – (On our blog : https://plantstomata.wordpress.com/2019/04/04/stomatal-transpiration-of-leaves/ )

Xu L., Baldocchi D. D. (2003) – Seasonal trends in photosynthetic parameters and stomatal conductance of blue oak (Quercus douglasii) under prolonged summer drought and high temperature – Tree Physiology 23: 865–877 – https://doi.org/10.1093/treephys/23.13.865 –https://academic.oup.com/treephys/article/23/13/865/1650675 – (On our blog : https://plantstomata.wordpress.com/2019/03/01/seasonal-trends-in-photosynthetic-parameters-and-stomatal-conductance/ )

Xu L., Najeeb U., Naeem M. S., Daud M. K., Cao J. S., Gong H. J., Shen W. Q., Zhou W. J. (2010) Induction of tetraploidy in Juncus effusus by colchicine – Biologia Plantarum 54(4): 659-663 – https://doi.org/10.1007/s10535-010-0117-9https://espace.library.uq.edu.au/view/UQ:721082 – (On our blog : https://plantstomata.wordpress.com/2020/02/19/differences-between-diploid-and-tetraploid-plants-larger-stomata-but-lower-stomatal-density-in-tetraploid-plants/ )

Xu M., Chen F., Qi S., Zhang L., Wu S. (2018) – Loss or duplication of key regulatory genes coincides with environmental adaptation of the stomatal complex in Nymphaea colorata and Kalanchoe laxiflora – Horticulture Research (2018)5: 42 – DOI 10.1038/s41438-018-0048-8 – Loss_or_duplication_of_key_regulatory_genes_coinci.pdf – (On our blog : https://plantstomata.wordpress.com/2018/09/09/loss-or-duplication-of-key-regulatory-genes-is-associated-with-environmental-adaptation-of-the-stomatal-complex/ )

Xu W., Li Y., Cheng Z., Xia G., Wang M. (2016) – A wheat histone variant gene TaH2A.7 enhances drought tolerance and promotes stomatal closure in Arabidopsis – Plant Cell Rep. 35(9): 1853-1862 – doi: 10.1007/s00299-016-1999-6 – Epub 2016 May 23 – PMID: 27215438 – https://pubmed.ncbi.nlm.nih.gov/27215438/ – (On our blog : https://plantstomata.wordpress.com/2022/03/10/tah2a-7-can-enhance-drought-tolerance-via-at-least-in-part-promoting-stomatal-closure/ )

Xu X., Chen Y., Li B., Zhang Z., Qin G., Chen T., Tian S. (2022) – How do horticultural crops defend themselves against fungal pathogens? – Horticulture Research 9: uhac066 – https://doi.org/10.1093/hr/uhac066 – EurekAlert! / AAAS – NANJING AGRICULTURAL UNIVERSITY THE ACADEMY OF SCIENCE – https://www.eurekalert.org/news-releases/961975 – (On our blog : https://plantstomata.wordpress.com/2022/08/19/research-progress-on-defense-responses-of-horticultural-crops-to-fungal-pathogens-and-novel-regulatory-strategies-to-regulate-induction-of-plant-resistance/ )

Xu X.-D., Lou C.-H. (1980)The presence of roots as a prerequisite for normal functioning of stomata on sweet potato leaves – Acta Agriculturae Universitatis Pekinensis (Journal of Peking Agricultural University) – (in Chinese) 1: 37-45 – ISSN :0479-8007 – https://www.cabdirect.org/cabdirect/abstract/19800712248 – (On our blog : https://plantstomata.wordpress.com/2019/03/30/a-physiologically-active-substance-from-roots-was-necessary-for-normal-stomatal-function/ )

Xu Y.-f.1, Chen H.1, Zhou H.2, Jin J.-w.1-3, Hu T.-m.1 (2011) – Acclimation of morphology and physiology in turf grass to low light environment: A review – African Journal of Biotechnology 10(48): 9737-9742 – http://www.academicjournals.org/AJBDOI: 10.5897/AJB11.1260 – ISSN 1684–5315 – file:///C:/Users/wille/Downloads/95744-Article%20Text-247816-1-10-20131024%20(2).pdf – (On our blog : https://plantstomata.wordpress.com/2022/09/13/plants-gain-limited-light-quantum-in-the-low-light-adversity-so-leaf-temperature-is-reduced-stomata-limitation-increased-stomata-conductance-decreased/ )

Xu Z., Jiang Y., Jia B., Zhou G. (2016) – Elevated-CO2 Response of Stomata and Its Dependence on Environmental Factors – Front. Plant Sci., 13 May 2016 – https://doi.org/10.3389/fpls.2016.00657 – https://www.frontiersin.org/articles/10.3389/fpls.2016.00657/full – (On our blog : https://plantstomata.wordpress.com/2018/01/24/how-stomata-respond-to-elevated-co2-levels-and-environmental-factors/ )

Xu Z. Z., Zhou G. (2008) – Responses of leaf stomatal density to water status and its relationship with photosynthesis in a grass – J. Exp. Bot. 59: 3317–3325 – DOI: 10.1093/jxb/ern185 – https://academic.oup.com/jxb/article-lookup/doi/10.1093/jxb/ern185 – (On our blog : https://plantstomata.wordpress.com/2017/06/15/stomatal-density-and-size/)

Xuan X., Wang Y., Ma S. M., Ye X.( 2011) – Comparisons between stomatal parameters between normal and abnormal leaf of Bougainvillea spectabilis Willd. – African Journal of Biotechnology 10(36): 6973-6978 – 94698-243748-1-PB.pdf – (On our blog : https://plantstomata.wordpress.com/2018/07/20/stomatal-parameters-of-normal-and-abnormal-leaves/ )

Xue S., Hu H., Ries A., Merilo E., Kollist H., Schroeder J. I. (2011) – Central functions of bicarbonate in S-type anion channel activation and OST1 protein kinase in CO2 signal transduction in guard cell – EMBO J. 30: 1645–1658 –  doi: 10.1038/emboj.2011.68 – http://labs.biology.ucsd.edu/schroeder/bggn227/oldfiles13/emboj201168%20Xue%20Hu%20et%20al.pdf – (On our blog : https://plantstomata.wordpress.com/2018/07/20/bicarbonate-in-s-type-anion-channel-activation-and-ost1-protein-kinase-in-co2-signal-transduction-in-stomata-2/

Xue S., Yang P. (2005) – Effects of La 3+ on inward K + channels at plasma membrane in guard cells – Science in China Series B Chemistry 48(2): 143-147 –https://www.researchgate.net/publication/244742609_Effects_of_La_3_on_inward_K_channels_at_plasma_membrane_in_guard_cells – (On our blog : https://plantstomata.wordpress.com/2017/12/14/effects-of-la-3-on-inward-k-channels-at-plasma-membrane-in-guard-cells/ )

Xue S. W., Hu H. H., Ries A., Merilo E., Kollist H., Schroeder J. I. (2011) – Central functions of bicarbonate in S-type anion channel activation and OST1 protein kinase in CO2 signal transduction in guard cell – Embo Journal 30: 1645-1658 – doi:10.1038/emboj.2011.68

Xue X., Bian C., Guo X., Di R., Dong J. (2020) – The MAPK substrate MASS proteins regulate stomatal development in Arabidopsis – PLOS Genetics 16(4): e1008706 – https://doi.org/10.1371/journal.pgen.1008706https://journals.plos.org/plosgenetics/article/comments?id=10.1371/journal.pgen.1008706 – (On our blog : https://plantstomata.wordpress.com/2020/07/25/mass-proteins-regulate-stomatal-development/ )

Yaaran A., Negin B., Moshelion M. (2017) – Role of guard-cell ABA in determining maximal stomatal aperture and prompt vapor-pressure-deficit response – Biorxiv – doi: https://doi.org/10.1101/218719 – https://www.biorxiv.org/content/early/2017/11/13/218719 – (On our blog : https://plantstomata.wordpress.com/2018/01/18/aba-maximal-stomatal-aperture-and-prompt-vapor-pressure-deficit-response/ )

Yamaguchi M., Kinose Y., Matsumura H., Izuta T. (2019) – Evaluation of O3 effects on cumulative photosynthetic CO2 uptake in seedlings of four Japanese deciduous broad-leaved forest tree species based on stomatal O3
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Yamamoto Y., Negi J., Wang C., Isogai Y., Schroeder J. I., Iba K . (2016) – The Transmembrane Region of Guard Cell SLAC1 Channels Perceives CO2 Signals via an ABA-Independent Pathway in Arabidopsis – Plant Cell.  28(2): 557-567 – Epub 2016 Jan 13 – https://doi.org/10.1105/tpc.15.00583http://www.plantcell.org/content/28/2/557 – (On our blog : https://plantstomata.wordpress.com/2019/03/01/stomatal-guard-cell-slac1-channels-perceives-co2-signals-via-an-aba-independent-pathway/ )

Yamamuro C., Miki D., Zheng Z., Ma J., Wang J., Yang Z., Dong J., Zhu J.-K. (2014) – Overproduction of stomatal lineage cells in Arabidopsis mutants defective in active DNA demethylation – Nat. Commun. 5: 4062 –

Yamasaki M., Moriya A. (1939) – Polyploidy and the size of stomata in the sugar-cane – Bot. Zool. 7: 1069-1072 – https://eurekamag.com/research/013/466/013466486.php – (On our blog : https://plantstomata.wordpress.com/2022/01/07/the-length-of-stomata-makes-it-possible-to-distinguish-easily-between-diploid-and-allopolyploid-strains/ )

Yamashita T. (1952) – Influences of potassium supply upon various properties and movement of guard cell – Sielboldia Acta Biollogy 1: 51–70 –

Yamauchi S., Mano S., Oikawa K., Hikino K., Teshima K. M., Kimori Y., Nishimura M., Shimazaki K.-i., Takemiya A. (2019) – Autophagy controls reactive oxygen species homeostasis in guard cells that is essential for stomatal opening – PNAS 116(38): 19187-19192 – https://doi.org/10.1073/pnas.1910886116https://www.pnas.org/content/116/38/19187 – (On our blog : https://plantstomata.wordpress.com/2019/10/15/autophagy-controls-stomatal-guard-cell-ros-homeostasis-by-eliminating-oxidized-peroxisomes-thereby-allowing-stomatal-opening/ )

Yamauchi S., Takemiya A., Sakamoto T., Kurata T., Tsutsumi T., Kinoshita T., Shimazaki K.-i. (2016)  The Plasma Membrane H+-ATPase AHA1 Plays a Major Role in Stomatal Opening in Response to Blue Light – Plant Physiology 171(4) – https://doi.org/10.1104/pp.16.01581 – http://www.plantphysiol.org/content/171/4/2731 – (On our blog : https://plantstomata.wordpress.com/2017/11/11/aha1-plays-a-major-role-in-stomatal-opening-in-response-to-blue-light/ )

Yamazaki D., Yoshida S., Asami T., Kuchitsu K. (2003) – Visualization of abscisic acid-perception sites on the plasma membrane of stomatal guard cells – Plant J. 35: 129–139 – doi: 10.1046/j.1365-313X.2003.01782.x — https://www.ncbi.nlm.nih.gov/pubmed/12834408 – (On our blog : https://plantstomata.wordpress.com/2018/01/17/visualization-of-the-aba-perception-sites-and-the-nature-of-membrane-associated-aba-receptors-in-stomata/ )

Yamazaki T., Kato K., Ito T., Nakai T., Matsumoto K., Miki N., Park H., Ohta T. (2013) – A common stomatal parameter set used to simulate the energy and water balance over boreal and temperate forests – Journal of the Meteorological Society of Japan 91: 273–285 – DOI: 10.2151/jmsj.2013-303https://www.jstage.jst.go.jp/article/jmsj/91/3/91_2013-303/_pdf – (On our blog : https://plantstomata.wordpress.com/2019/03/01/a-common-stomatal-parameter-set-used-to-simulate-the-energy-and-water-balance-over-boreal-and-temperate-forests/ )

Yamori W., Kusumi K., Iba K., Terashima I. (2020) – Increased stomatal conductance induces rapid changes to photosynthetic rate in response to naturally fluctuating light conditions in rice – Plant, Cell & Environment – https://doi.org/10.1111/pce.13725https://onlinelibrary.wiley.com/doi/abs/10.1111/pce.13725 – (On our blog : https://plantstomata.wordpress.com/2020/08/15/increased-stomatal-conductance-induces-rapid-changes-to-photosynthetic-rate/ )

Yan F., Li X., Liu F. (2017) – ABA signaling and stomatal control in tomato plants exposure to progressive soil drying under ambient and elevated atmospheric CO2 concentration – Environ. Exp. Bot. 139: 99–104 – https://doi.org/10.1016/j.envexpbot.2017.04.008https://www.sciencedirect.com/science/article/abs/pii/S009884721730103X?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/09/27/aba-signaling-and-stomatal-control/ )

Yan F., Liu F. (2016) – Effects of different concentration of Ca (NO 3)on quinoa treated with salinity – Peer J. Preprints 4:e1956v1 – https://doi.org/10.7287/peerj.preprints.1956v1https://peerj.com/preprints/1956/ – (On our blog : https://plantstomata.wordpress.com/2021/12/11/stomata-and-the-effects-of-cano3-2-applications/ )

Yan F., Sun Y., Song F., Liu F. (2012) – Differential responses of stomatal morphology to partial root-zone drying and deficit irrigation in potato leaves under varied nitrogen rates – Scientia Horticulturae 145: 76-83 – https://doi.org/10.1016/j.scienta.2012.07.026 – https://www.sciencedirect.com/science/article/pii/S0304423812003573 – (On our blog : https://plantstomata.wordpress.com/2018/02/04/partial-root-zone-drying-prd-reduces-plant-water-use-via-modulating-stomatal-morphology-under-high-n-rate/

Yan G., Alassimone J., Varnau R., Sharma N., Cheung L. S., Bergmann D. C.  (2021) – Tuning self-renewal in the Arabidopsis stomatal lineage by hormone and nutrient regulation of asymmetric cell division – eLife 10:e63335 – DOI: 10.7554/eLife.63335https://elifesciences.org/articles/63335 – (On our blog : https://plantstomata.wordpress.com/2022/03/31/a-mechanistic-understanding-of-how-nutritional-status-and-environmental-factors-tune-stem-cell-behavior-in-the-stomatal-lineage/ )

Yan J., Yu H., Li B., Fan A., Melkonian J., Wang X., Zhou T., Hua J. (2019) – Cell autonomous and non-autonomous functions of plant intracellular immune receptors in stomatal defense and apoplastic defense – PloS Pathog 15(10): e1008094 – https://doi.org/10.1371/journal.ppat.1008094https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008094 – (On our blog : https://plantstomata.wordpress.com/2020/02/29/an-unexpected-regulation-of-stomatal-defense-by-nlr-genes/ )

Yan W., Zhong Y., Shangguan Z. (2017) – Contrasting responses of leaf stomatal characteristics to climate change: a considerable challenge to predict carbon and water cycles – Glob. Change Biol. 104: 145–157 – doi: 10.1111/gcb.13654 – https://onlinelibrary.wiley.com/doi/abs/10.1111/gcb.13654 https://plantstomata.wordpress.com/2019/03/01/a-common-stomatal-parameter-set-used-to-simulate-the-energy-and-water-balance-over-boreal-and-temperate-forests/)

Yáñez M. A., Urzua J. I., Espinoza S. E., Peña V. L. (2021) – Limited Phenotypic Variation in Vulnerability to Cavitation and Stomatal Sensitivity to Vapor Pressure Deficit among Clones of Aristotelia chilensis from Different Climatic Origins – Plants (Basel) 10(9): 1777 – doi: 10.3390/plants10091777 – PMID: 34579309 – PMCID: PMC8469263 – https://pubmed.ncbi.nlm.nih.gov/34579309/ – (On our blog : https://plantstomata.wordpress.com/2021/12/26/stomatal-sensitivity-to-vapor-pressure-deficit-3/ )

Yang C., Jinyu S., Du X., Hui D., Liang M. (1998) – Studies on the stomata of apple leaves – J. Shandong Agril. Univ. 29: 8-14 – https://europepmc.org/article/cba/313244 – (On our blog : https://plantstomata.wordpress.com/2021/04/18/stomata-are-of-stable-heredity-character-an-microcosmic-morphological-character-when-studing-the-heredity-breeding-of-fruit-trees-distinguishing-cultivars-and-strains/ )

Yang D. L., Shi Z., Bao Y., Yan J., Yang Z., Yu H., Li Y., Gou M., Wang S., Zou B., Xu D., Ma Z., Kim J., Hua J. (2017) – Calcium Pumps and Interacting BON1 Protein Modulate Calcium Signature, Stomatal Closure, and Plant Immunity – Plant Physiology 175(1): –  https://doi.org/10.1104/pp.17.01136 – http://www.plantphysiol.org/content/175/1 – (On our blog : https://plantstomata.wordpress.com/2017/11/12/aca10-8-and-bon1-interact-on-plasma-membrane-and-function-in-the-generation-of-cytosol-calcium-signatures-critical-for-stomatal-movement/

Yang F., Devetter L.W., Strik B.C., Bryla D.R. (2019) – Stomatal functioning and its influence on calcium accumulation during fruit development in northern highbush blueberry – HortScience. 53(9): 96-102 – https://doi.org/10.21273/HORTSCI14482-19https://www.ars.usda.gov/research/publications/publication/?seqNo115=352174 – (On our blog : https://plantstomata.wordpress.com/2019/12/09/although-stomatal-conductance-is-low-in-developing-blueberries-it-appears-to-be-an-important-mechanism-by-which-ca-is-delivered-to-the-berries/ )

Yang H. M. (2004) – Studies on the physiological and molecular regulation mechanisms of stomatal oscillation – PhD thesis, University of Lanzhou, China.

Yang H. M., Wang G. X. (2001) – Leaf stomatal densities and distribution in Triticum aestivum under drought and CO2 enrichment – Acta Phytoecologica Sinica 25: 312–316 – https://europepmc.org/abstract/cba/540904 – (on our blog : https://plantstomata.wordpress.com/2019/03/02/leaf-stomatal-densities-and-distribution-under-drought-and-co2-enrichment/ )

Yang H. M., Zhang X. Y., Tang Q.-L., Wang G.-X. (2006)  Extracellular calcium is involved in stomatal movement through the regulation of water channels in broad bean – Plant Growth Regulation 50(1): 79-83 – DOI: 10.1007/s10725-006-9128-0 –https://www.infona.pl/resource/bwmeta1.element.springer-6f95dbbd-1b60-3c0e-baed-9c2cbcc6471f – (On our blog : https://plantstomata.wordpress.com/2017/10/24/extracellular-calcium-and-the-regulation-of-water-channels-in-stomatal-movement/ )

Yang H. M., Zhang X. Y., Wang G.X. (2004) – Cytosolic calcium oscillation signaling in guard cell – Plant Science 166: 549-556 – https://doi.org/10.1016/j.plantsci.2003.11.005 –https://www.sciencedirect.com/science/article/pii/S0168945203004813 – (On our blog : https://plantstomata.wordpress.com/2019/03/02/how-ca2cyt-oscillations-are-encoded-and-decoded-and-water-channels-may-be-involved-in-stomatal-oscillation/ )

Yang H. M., Zhang X. Y., Wang G.X. (2004) – Effects of heavy metals on stomatal movements in broad bean leaves – Russian Journ. Plant Physiol. 51(4): 464-468 (Fiziologiya Rastenii 51(4): 516-520) – http://www.paper.edu.cn/scholar/showpdf/MUT2MNxINTj0Axwh – (On our blog : https://plantstomata.wordpress.com/2021/01/23/effects-of-heavy-metals-on-stomatal-movements/ )

Yang H. M., Zhang J., Zhang X. (2005) – Regulation mechanisms of stomatal oscillation – Journal of Integrative Plant Biology 47: 1159–1172 – https://doi.org/10.1111/j.1744-7909.2005.00146.x – https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1744-7909.2005.00146.x – (On our blog : https://plantstomata.wordpress.com/2018/10/28/a-summary-of-studies-on-stomatal-oscillation-and-a-discussion-regarding-the-mechanisms-of-regulation-of-stomatal-oscillation/ )

Yang J., Li C., Kong D., Guo F., Wei H. (2020) – Light-Mediated Signaling and Metabolic Changes Coordinate Stomatal Opening and Closure – Front. Plant Sci., 04 December 2020 | https://doi.org/10.3389/fpls.2020.601478https://www.frontiersin.org/articles/10.3389/fpls.2020.601478/full – (On our blog : https://plantstomata.wordpress.com/2021/03/27/mechanisms-regulating-the-trade-off-between-stomatal-opening-and-closure-may-have-potential-applications-toward-generating-superior-crops-with-improved-water-use-efficiency/ )

Yang J., Liang T., Liu L., Pan T., Zou Z. (2019) – Stomatal opening and growth in tomato seedlings treated with different proportions of red and blue light – Canadian Journal of Plant Science 99(5): 688-700 – https://doi.org/10.1139/cjps-2018-0241https://www.nrcresearchpress.com/doi/abs/10.1139/CJPS-2018-0241 – (On our blog : https://plantstomata.wordpress.com/2020/09/08/red-and-blue-light-dependent-stomatal-opening-processes/ )

Yang J., Ordiz I. M., Jaworski J. G., Beachy, R. N. (2011) – Induced accumulation of cuticular waxes enhances drought tolerance in Arabidopsis by changes in development of stomata – Plant Physiol. Biochem. 49: 1448–1455 – doi: 10.1016/j.plaphy.2011.09.006https://www.sciencedirect.com/science/article/abs/pii/S0981942811002580?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/12/29/drought-tolerance-caused-by-the-induction-of-win1-shin-gene-may-be-due-to-reduced-numbers-of-stomata-as-well-as-to-cuticular-wax-accumulation/ )

Yang J., Weyers J., Zhu Q., Peng Z. (1995) – Effect of water deficit stress on the stomatal frequency, stomatal conductance and abscisic acid in rice leaves – Acta Agronomica Sinica 21: 533–539 – https://europepmc.org/abstract/cba/282006 – (On our blog : https://plantstomata.wordpress.com/2019/03/02/effect-of-water-deficit-stress-on-stomatal-frequency-and-stomatal-conductance/ )

Yang J., Weyers J., Zhu Q., Peng Z. (1995) – Effect of water deficit stress on the stomatal frequency, stomatal conductance and abscisic acid in rice leaves – Acta Agron. Sin. 21: 533– 539 – https://europepmc.org/article/cba/282006 – (On our blog : https://plantstomata.wordpress.com/2020/11/04/effect-of-water-deficit-stress-on-the-stomatal-frequency-stomatal-conductance-and-aba/ )

Yang K., Jiang M., Le J. (2014) – A new loss‐of‐function allele 28y reveals a role of ARGONAUTE1 in limiting asymmetric division of stomatal lineage ground cell – Journal of Integrative Plant Biology 56(6): – https://doi.org/10.1111/jipb.12154https://onlinelibrary.wiley.com/doi/abs/10.1111/jipb.12154 – (On our blog : https://plantstomata.wordpress.com/2020/04/08/upregulation-of-agamous%e2%80%90like16-agl16-in-28y-mutants-suggests-that-ago1-is-required-to-restrict-agl16%e2%80%90mediated-stomatal-spacing-divisions/ )

Yang K., Jiang M., Wang M., Xue S., Zhu L.-l., Wang H.-Z., Zou J., Lee E.-K., Sack F. D., Le J. (2015) – Phosphorylation of Serine 186 of bHLH Transcription Factor SPEECHLESS Promotes Stomatal Development in Arabidopsis – Molecular Plant 8(5): 783-795 – https://doi.org/10.1016/j.molp.2014.12.014 –https://www.sciencedirect.com/science/article/pii/S1674205214000513 – (On our blog : https://plantstomata.wordpress.com/2019/03/02/phosphorylation-of-serine-186-of-bhlh-transcription-factor-speechless-promotes-stomatal-development/ )

Yang K., Le J. (2019) – A conserved but plant specific CDK-mediated regulation of DNA replication protein A2 in the precise control of stomatal terminal division – PNAS – See : Scientists find precise control of terminal division during plant stomatal developmenthttps://phys.org/news/2019-08-scientists-precise-terminal-division-stomatal.html – (On our blog : https://plantstomata.wordpress.com/2020/08/02/scientists-find-precise-control-of-terminal-division-during-plant-stomatal-development/ )

Yang K., Zhu L., Wang H., Jiang M., Xiao C., Hu X., Vanneste S., Dong J., Le J. (2019) – A conserved but plant-specific CDK-mediated regulation of DNA replication protein A2 in the precise control of stomatal terminal division – PNAS 116(36): 18126-18131- https://doi.org/10.1073/pnas.1819345116https://www.pnas.org/content/early/2019/08/19/1819345116 – (On our blog : https://plantstomata.wordpress.com/2019/08/21/the-precise-control-of-stomatal-terminal-division/ )

Yang K.-T., Chang H.-L., Chen G.-P., Yu X.-Y., Xian J.-R. (2021) – Stomatal traits of main greening plant species in Lanzhou – Chin J Plant Ecol  45(2): 187-196 – DOI: 10.17521/cjpe.2020.0257https://www.plant-ecology.com/EN/10.17521/cjpe.2020.0257 – (On our blog : https://plantstomata.wordpress.com/2021/11/28/96405/ )

Yang L., Mei H., Zhou G., Li J. (2007) – The changes of water-use efficiency and stoma density of Leymus chinensis along Northeast China Transect – Acta Ecologica Sinica 27: 16–24 – https://doi.org/10.1016/S1872-2032(07)60006-7 –https://www.sciencedirect.com/science/article/pii/S1872203207600067 –  https://plantstomata.wordpress.com/2016/02/16/water-use-efficiency-and-stoma-density/ )

Yang L.-N., Liu H., Wang Y.-P., Seemlatti J., Grenville-Briggs L. J., Wang Z., Zhan J. (2021) – Pathogen-Mediated Stomatal Opening: A Previously Overlooked Pathogenicity Strategy in the Oomycete Pathogen Phytophthora infestans – Front. Plant Sci., 12 July 2021 – https://doi.org/10.3389/fpls.2021.668797https://www.frontiersin.org/articles/10.3389/fpls.2021.668797/full – (On our blog : https://plantstomata.wordpress.com/2021/11/09/95163/ )

Yang M., Sack F. D. (1995) – The too many mouths and four lips mutations affect stomatal production in Arabidopsis – Plant Cell 7: 2227–2239 – doi: 10.1105/tpc.7.12.2227 – https://www.jstor.org/stable/3870164?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2018/03/22/two-mutations-affect-stomatal-production-more-than-patterning-or-differentiation/ )

Yang S., Liu X., Tyree M. T. (1998) – A model of stomatal conductance in sugar maple (Acer saccharum Marsh) – J Theor Biol 191: 197–211 –

Yang S. H., Berberich T., Sano H., Kusano T. (2001) – Specific association of transcripts of tbzF and tbz17, tobacco genes encoding basic region leucine zipper-type transcriptional activators, with guard cells of senescing leaves and/or flowers – Plant Physiol. 127(1): 23-32 – doi: 10.1104/pp.127.1.23 – PMID: 11553731 – PMCID: PMC117959 – https://pubmed.ncbi.nlm.nih.gov/11553731/ – (On our blog : https://plantstomata.wordpress.com/2021/04/25/tbzf-and-tbz17-are-both-involved-in-controlling-gene-transcription-related-to-functions-of-stomata-in-senescing-leaves-tbzf-acts-bifunctionally-in-floral-development/ )

Yang S.-L., Ho C.-M. K. (2022) – The coordination between stomata and cuticles – The Plant Cell: In a Nutshell February 15, 2022 – https://plantae.org/the-coordination-between-stomata-and-cuticles/ – (On our blog : https://plantstomata.wordpress.com/2022/04/22/coordination-between-stomata-and-cuticles/ )

Yang S.-L., Tran N., Tsai M.-Y., Ho C.-M. K. (2021) – Misregulation of MYB16 expression causes stomatal cluster formation by disrupting polarity during asymmetric cell divisions – The Plant Cell – koab260 – https://doi.org/10.1093/plcell/koab260https://academic.oup.com/plcell/advance-article-abstract/doi/10.1093/plcell/koab260/6412568 – (On our blog : https://plantstomata.wordpress.com/2021/11/27/96281/ )

Yang T. Z., Yu Y. Q., Le D. Y., Mei Z. Y. (2004) – Relationships between ozone injury and stoma parameters and activities of antioxidant enzyme – Acta-Phytoecologica_Sinica 28: 672-679 – https://europepmc.org/abstract/cba/465258 – (On our blog : https://plantstomata.wordpress.com/2019/07/17/ozone-injury-stoma-parameters-and-activities-of-antioxidant-enzyme/ )

Yang T. Z., Zhang X. Y., Wang G. X. (2004) – Relationships between stomatal character, photosynthetic character and seed chemical composition in grass pea at different water availabilities – Journal of Agricultural Science 142: 675-681 –  https://agris.fao.org/agris-search/search.do?recordID=US201301014975 – (On our blog : https://plantstomata.wordpress.com/2020/12/08/stomatal-aperture-may-be-more-closely-related-to-photosynthetic-character-and-seed-chemical-composition-in-grass-pea-and-water-deficit-may-enhance-the-correlations/ )

Yang W., Ruan M., Xiang M., Deng A., Du J., Xiao C. (2019) – Overexpression of a pectin methylesterase gene PtoPME35 from Populus tomentosa influences stomatal function and drought tolerance in Arabidopsis thaliana – BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS

Yang X. et al. (2017) – Drought-resistant plant genes could accelerate evolution of water-use efficient crops – https://phys.org/news/2017-12-drought-resistant-genes-evolution-water-use-efficient.html#jCp – (On our blog : https://plantstomata.wordpress.com/2017/12/02/stomata-cam-plants-water-use-efficiency-and-drought-resistant-plant-genes/ )

Yang X., Short T. H., Fox R. D., Bauerle W. L. (1990) – Transpiration, leaf temperature and stomatal resistance of a greenhouse cucumber crop – Agricultural and Forest Meteorology 51(3-4): 197-209 – https://doi.org/10.1016/0168-1923(90)90108-Ihttps://www.sciencedirect.com/science/article/abs/pii/016819239090108I – (On our blog : https://plantstomata.wordpress.com/2021/03/31/no-significant-correlations-between-stomatal-resistance-and-other-climatic-variables/ )

Yang X., Yang Y., Ji C., Feng T., Shi Y., Lin L., Ma J., He J.-S. (2014) – Large-scale patterns of stomatal traits in Tibetan and Mongolian grassland species – Basic and Applied Ecology 15(2): 122-132 – https://doi.org/10.1016/j.baae.2014.01.003 –https://www.sciencedirect.com/science/article/pii/S1439179114000048?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/04/01/the-low-temperature-and-high-insolation-at-high-altitudes-may-be-responsible-for-the-larger-and-fewer-stomata/ )

Yang Y., Chen J., Liu Q., Ben C., Todd C. D., Shi J., Yang Y., Hu X. (2012) – Comparative proteomic analysis of the thermotolerant plant Portulaca oleracea acclimation to combined high temperature and humidity stress – J Proteome Res. 11(7): 3605-3623 – doi: 10.1021/pr300027a – Epub 2012 Jun 7 – PMID: 22616707 – https://pubmed.ncbi.nlm.nih.gov/22616707/ – (On our blog : https://plantstomata.wordpress.com/2022/09/11/quickly-accumulations-of-proline-content-and-heat-shock-proteins-and-depleting-aba-were-also-found-in-portulaca-oleracea-under-stress-conditions-that-resulted-into-greater-stomata-conductance/ )

Yang Y., Costa A., Leonhardt N., Siegel R. S., Schroeder J. I. (2008) – Isolation of a strong Arabidopsis guard cell promoter and its potential as a research tool – Plant Methods 4: 6 – https://doi.org/10.1186/1746-4811-4-6 – https://plantmethods.biomedcentral.com/articles/10.1186/1746-4811-4-6 – (On our blog : https://plantstomata.wordpress.com/2018/01/18/isolation-of-a-strong-arabidopsis-guard-cell-promoter-and-its-potential-as-a-research-tool/ )

Yang Y., Yu L., Wang L., Guo S. (2015) – Bottle gourd rootstock-grafting promotes photosynthesis by regulating the stomata and non-stomata performances in leaves of watermelon seedlings under NaCl stress – Science.gov (United States) – https://worldwidescience.org/topicpages/c/closing+plant+stomata.html – (On our blog : https://plantstomata.wordpress.com/2022/03/06/promotion-of-photosynthesis-by-the-activation-of-stomatal-and-non-stomatal-abilities-especially-the-regulation-of-a-variety-of-photosynthetic-enzymes/ )

Yang Y.-J., Bi M., Nie Z., Jiang H., Liu X., Fang X., Brodribb T. J., (2021) – Evolution of stomatal closure to optimise water use efficiency in response to dehydration in ferns and seed plants – New Phytologist – DOI: 10.1111/nph.17278https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.17278https://www.researchgate.net/publication/349314771_Evolution_of_stomatal_closure_to_optimise_water_use_efficiency_in_response_to_dehydration_in_ferns_and_seed_plants – (On our blog : https://plantstomata.wordpress.com/2021/02/24/evolution-of-stomatal-closure-to-optimise-water-use-efficiency-in-response-to-dehydration/ )

Yang Z. Q., Tan W., Liu Z. X., Chen Y. Q. (2015) – Effect of soil water stress on stomatal characters of greenhouse tomato leaves – Chinese Journal of Ecology 34: 1234-1240 –


[ 杨再强, 谭文, 刘朝霞, 陈艳秋 (2015). 土壤水分胁迫对设施番茄叶片气孔特性的影响. 生态学杂志, 34,1234-1240.]

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Zeiger E., Stebbins L. (1972) – Developmental genetics in barley: a mutant for stomatal development – American Journal of Botany 59: 143–148 – https://doi.org/10.1002/j.1537-2197.1972.tb10073.xhttps://bsapubs.onlinelibrary.wiley.com/doi/10.1002/j.1537-2197.1972.tb10073.x – (On our blog : https://plantstomata.wordpress.com/2022/07/06/an-abnormal-stomatal-development-as-a-pleiotropic-effect-2/)

Zeiger E., Talbott L. D., Frechilla S., Srivastava A., Zhu J. (2002) – The guard cell chloroplast: a perspective for the twenty-first century – New Phytol 153: 415–424 – https://doi.org/10.1046/j.0028-646X.2001.NPH328.doc.x – https://nph.onlinelibrary.wiley.com/doi/full/10.1046/j.0028-646X.2001.NPH328.doc.x – (On our blog : https://plantstomata.wordpress.com/2018/10/05/the-properties-of-the-stomatal-chloroplast/ )

Zeiger E., Zhu J. (1998) – Role of zeaxanthin in blue light photoreception and the modulation of light-CO2 interactions in guard cells – J. Exp. Bot. 49: 433–442 – DOI: 10.1093/jxb/49.Special_Issue.433 – https://www.jstor.org/stable/23695976?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2018/07/21/blue-light-sensing-by-guard-cell-zeaxanthin-has-a-regulatory-role-in-the-light-response-of-stomata/

Zeilinger C., Palme K., Hedrich R. (1992) – Identification of a potassium channel in mesophyll and guard cell plasma membranes of Vicia faba leaves – 9th International workshop on plant membrane biology, Monterey July 19-24, 1992, Abstr. No. 51 –

Zelitch I. (1961) – Biochemical control of stomatal opening in leaves – Proc. Natl. Acad. Sci. U. S. 47: 1423-1433 – doi: 10.1073/pnas.47.9.1423https://www.ncbi.nlm.nih.gov/pmc/articles/PMC223154/ – (On our blog : https://plantstomata.wordpress.com/2021/12/04/biochemical-control-of-stomatal-opening/ )

Zelitch I. (1963) Stomata and water relations in plants – Advanced Science Seminar on the Physiology and Biochemistry of Leaf Stomata – Conn. Agric. Expt. Sta.,  Bull. 664. 116 pp – http://www.ct.gov/caes/lib/caes/documents/publications/bulletins/b664.pdf – (On our blog : https://plantstomata.wordpress.com/2017/11/22/stomata-and-water-relations/ )

Zelitch I. (1963) – The control and mechanism of stomatal movement. In: Stomata and water relations in plants – Bull. Conn, Agric. Exp. Stn. 664: 18 –

Zelitch I. (1964)  Stomata and Water Relationships in Plants – Soil Science:  98(1): 347 https://journals.lww.com/soilsci/Citation/1964/11000/Stomata_and_Water_Relationships_in_Plants.15.aspx – (On our blog : https://plantstomata.wordpress.com/2021/11/19/stomata-and-water/ )

Zelitch I. (1965) – Environmental and biochemical control of stomatal movement in leaves – Biological Reviews 40(4): 463-481 –  https://doi.org/10.1111/j.1469-185X.1965.tb00811.x – https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1469-185X.1965.tb00811.x – (On our blog : https://plantstomata.wordpress.com/2019/03/03/environmental-and-biochemical-control-of-stomatal-movement/ )

Zelitch I. (1967) – Control of leaf stomata – Their role in transpiration and photosynthesis – American Scientist 55(4): 472-486 – https://www.jstor.org/stable/27837040?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2019/01/08/the-role-of-stomata-in-transpiration-and-photosynthesis/ )

Zelitch I. (1969) – Stomatal control – Annual Review of Plant Biology 20(1): 329-350 – https://doi.org/10.1146/annurev.pp.20.060169.001553 –https://app.dimensions.ai/details/publication/pub.1018400569 – (On our blog : https://plantstomata.wordpress.com/2019/01/30/stomatal-control/ )

Zelitch I. (1969) – Mechanisms of Carbon Fixation and Associated Physiological Responses – Agronomy & Horticulture Department at DigitalCommons@University of Nebraska – Lincoln – Faculty Publications 198 – https://digitalcommons.unl.edu/agronomyfacpub/198 – Published in Physiological Aspects of Crop Yield: Proceedings of a symposium January 20-24, 1969. Edited by Jerry D. Eastin, F. A. Haskins, C. Y. Sullivan, C. H. M. Van Bavel, and Richard C. Dinauer (Madison, Wisconsin: American Society of Agronomy & Crop Science Society of America, 1969) – https://digitalcommons.unl.edu/cgi/viewcontent.cgi?article=1191&context=agronomyfacpub;Mechanisms – (On our blog : https://plantstomata.wordpress.com/2021/11/13/stomatal-opening-in-light-and-inhibitors-of-stomatal-opening/ )

Zelitch I., Waggoner P. E. (1962) – Effect of chemical control of stomata on transpiration and photosynthesis – Proc. Natl. Acad. Sci. U. S. 48: 1101-1108 – PNAS 48(7): 1101-1108 – https://doi.org/10.1073/pnas.48.7.1101https://www.pnas.org/content/48/7/1101 – (On our blog : https://plantstomata.wordpress.com/2021/11/19/chemical-control-of-stomata-on-transpiration-and-photosynthesis/ )

Zelitch I., Waggoner P. E. (1962) – Effect of chemical control of stomata on transpiration of intact plants – PNAS 48(8): 1297-1299 – https://doi.org/10.1073/pnas.48.8.1297https://www.pnas.org/content/48/8/1297 – (On our blog : https://plantstomata.wordpress.com/2021/11/20/chemical-control-of-stomata-on-transpiration/ )

Zelitch I., Walker D. A. (1964) – The role of glycolic acid metabolism in opening of leaf stomata – Plant Physiol. 39: 856-862 –

Zemel E., Gepstein S. (1985) – Immunological evidence for the presence of ribulose bisphosphate carboxylase in guard cell chloroplasts – Plant Physiol. 78: 586–590 – https://doi.org/10.1104/pp.78.3.586http://www.plantphysiol.org/content/78/3/586 – (On our blog : https://plantstomata.wordpress.com/2019/03/03/ribulose-bisphosphate-carboxylase-in-stomatal-guard-cell-chloroplasts/ )

Zenes N., Kerr K. L., Trugman A. T., Anderegg W. R. L. (2020) – Competition and Drought Alter Optimal Stomatal Strategy in Tree Seedlings – Front. Plant Sci., 08 May 2020 – https://doi.org/10.3389/fpls.2020.00478https://www.frontiersin.org/articles/10.3389/fpls.2020.00478/full – (On our blog : https://plantstomata.wordpress.com/2021/10/19/stomatal-strategies-are-dynamic-and-change-with-climate-and-competition-stressors/ )

Zeng S. M., Lo E. K. W., Hazelton B. J., Morales M. F., Torii K. U. (2020) – Effective range of non-cell autonomous activator and inhibitor peptides specifying plant stomatal patterning – Development 147: dev192237 – doi: 10.1242/dev.192237https://dev.biologists.org/content/147/17/dev192237 – (On our blog : https://plantstomata.wordpress.com/2020/09/24/non-cell-autonomous-activator-and-inhibitor-peptides-specifying-plant-stomatal-patterning/ )

Zeng W., Brutus A., Kremer J. M., Withers J. C., Gao X., Jones A. D., He S. Y. (2011) – A genetic screen reveals Arabidopsis stomatal and/or apoplastic defenses against Pseudomonas syringae pv. tomato DC3000 – PLoS Pathog. 2011 Oct.7(10):e1002291 – doi: 10.1371/journal.ppat.1002291 – Epub 2011 Oct 6 – https://www.ncbi.nlm.nih.gov/pubmed/21998587 – (On our blog : https://plantstomata.wordpress.com/2019/12/07/identification-of-scord5-begins-to-implicate-an-important-role-of-stress-associated-protein-translation-in-stomatal-guard-cell-signaling-in-response-to-microbe-associated-molecular-patterns-and-bacter/ )

Zeng W., He S. Y. (2010) – A prominent role of the flagellin receptor FLAGELLIN-SENSING2 in mediating stomatal response to Pseudomonas syringae pv tomato DC3000 in Arabidopsis – Plant Physiol. 153: 1188–1198 – doi: 10.1104/pp.110.157016 – http://www.plantphysiol.org/content/153/3/1188 – (On our blog : https://plantstomata.wordpress.com/2018/07/22/the-flagellin-receptor-flagellin-sensing2-in-mediating-stomatal-response-to-pseudomonas-syringae/ )

Zeng W., Melotto M., He S. Y. (2010) – Plant stomata: a checkpoint of host immunity and pathogen virulence – Curr. Opin. Biotechnol. 21: 599–603 – doi: 10.1016/j.copbio.2010.05.006 – https://www.ncbi.nlm.nih.gov/pubmed/20573499 – (On our blog : https://plantstomata.wordpress.com/2018/07/22/signaling-events-involved-in-bacterium-triggered-stomatal-closure-and-virulence-factors-to-actively-counter-stomatal-closure-to-facilitate-invasion/ )

Responses of two semiarid conifer tree species to reduced precipitation and warming reveal new perspectives for stomatal regulation – Plant, Cell & Environment

Zeppel M., Lewis J. D., Chaszar B., Smith R. A., Medlyn B. E., Huxman T. E., Tissue D. T. (2012) – Nocturnal stomatal conductance responses to rising [CO2], temperature and drought –  New Phytol. 193: 929–938 – Doi: 10.1111/j.1469-8137.2011.03993.x -yhttps://www.ncbi.nlm.nih.gov/pubmed/22150067 – (On our blog : https://plantstomata.wordpress.com/2019/03/03/nocturnal-stomatal-conductance-responses-to-rising-co2-temperature-and-drought/ )

Zeppel M., Logan B., Lewis D., Phillips N. Tissue D. (2013) – Why lose water at night? Disentangling the mystery of nocturnal sap flow, transpiration and stomatal conductance – When, where, who? – Acta Horticulturae 991: 307-312 – International Workshop on Sap Flow (9th : 2013) – Ghent, Belgium – https://researchers.mq.edu.au/en/publications/why-lose-water-at-night-disentangling-the-mystery-of-nocturnal-sa – (On our blog : https://plantstomata.wordpress.com/2022/01/06/nocturnal-sap-flow-transpiration-and-stomatal-conductance/ )

Zeppel M., Macinnis-Ng C. M. O., Yunusa I. A. M., Whitley R. J.Eamus D. (2008) – Long term trends of stand transpiration in a remnant forest during wet and dry years – Journal of Hydrology 349: 200 – 213 – doi:10.1016/j.jhydrol.2007.11.001https://www.academia.edu/13850056/Long_term_trends_of_stand_transpiration_in_a_remnant_forest_during_wet_and_dry_years?email_work_card=view-paper – (On our blog : https://plantstomata.wordpress.com/2021/04/07/89648/ )

Zgallai H., Steppe K., Lemeur R. (2006) – Effects of different levels of water stress on leaf water potential, stomatal resistance, protein and chlorophyll content and certain anti-oxidative enzymes in tomato plants – Journal of Integrative Plant biology 48(6): 679-685 – https://doi.org/10.1111/j.1744-7909.2006.00272.xhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1744-7909.2006.00272.x -n (On our blog : https://plantstomata.wordpress.com/2020/04/10/effects-of-different-levels-of-water-stress-on-leaf-water-potential-and-stomatal-resistance/ )

Zhang A., Huang R., Wang X., Yuan M. (2001) – Identification of integrin-like in guard cells of Vicia faba – Chinese Science Bulletin 46: 1100–1102 – https://doi.org/10.1007/BF02900687https://link.springer.com/article/10.1007/BF02900687 – (On our blog : https://plantstomata.wordpress.com/2019/03/04/integrins-like-are-present-at-the-stomatal-guard-cell-plasma-membrane/ )

Zhang A., Ren H. M., Tan Y. Q., Qi G. N., Yao F. Y., Wu G. L., Yang L. W., Hussain J., Sun S. J., Wang Y. F. (2016) – S-type Anion Channels SLAC1 and SLAH3 Function as Essential Negative Regulators of Inward K+ Channels and Stomatal Opening in Arabidopsis – Plant Cell. 28(4): 949-955 – doi: 10.1105/tpc.16.01050http://www.plantcell.org/content/28/4/949 – (On our blog : https://plantstomata.wordpress.com/2019/03/11/a-novel-regulatory-mechanism-for-stomatal-movement-2/ )

Zhang B., Liu Y., Xu D., Cai J., Zhao N. (2011) – Estimation of summer corn canopy conductance by scaling up leaf stomatal conductance – Transactions of the CSAE 27: 80–86 – [In Chinese with English summary] – https://www.ingentaconnect.com/content/tcsae/tcsae/2011/00000027/00000005/art00013 – (On our blog : https://plantstomata.wordpress.com/2019/03/04/leaf-stomatal-conductance-gs-and-canopy-conductance-gc/ )

Zhang C., Huang H., Zhou Y., Lin H., Xie T., Liao C. (2019) – Stomatal Response of Maize (Zea mays L.) to Crude Oil Contamination in Soils – Appl. Sci. 9: 4074 – doi:10.3390/app9194074 – applsci-09-04074 – (On our blog : https://plantstomata.wordpress.com/2020/03/02/controlling-stomata-movement-will-be-beneficial-to-phytoremediation-of-contaminated-soil/ )

Zhang D., Liu Y., Zhang H., Zhang Z.-J., Wang Y., Liu M.-C. (2021) – Response of Photosynthesis and Leaf Morphological Characteristics to Drought Stress in Glycyrrhiza uralensis – Bulletin Bot. Res. (BBR) 41(3): 449-457 – doi: 10.7525/j.issn.1673-5102.2021.03.016http://bbr.nefu.edu.cn/article/2021/1673-5102/1673-5102-2021-41-3-449.shtml – (On our blog : https://plantstomata.wordpress.com/2022/03/31/severe-drought-stress-accelerated-the-programmed-death-of-stomatal-cells-pcd-and-seedlings-lost-their-ability-to-resist-drought/ )

Zhang D., Tian C., Yin K., Wang W., Qiu J. L. ( 2019) – Postinvasive Bacterial Resistance Conferred by Open Stomata in Rice – Mol Plant Microbe Interact. 32(2): 255-266 – doi: 10.1094/MPMI-06-18-0162-Rhttps://www.ncbi.nlm.nih.gov/pubmed/30124364 – (On our blog : https://plantstomata.wordpress.com/2019/04/06/a-novel-role-of-stomata-in-plant-immunity-through-modulation-of-leaf-water-status/ )

Zhang D. C., Zhu Y. H., Li S. Z. (2018) – Variation in stomatal characteristics of eight plant species along a soil moisture gradient in alpine meadow of the Dongda Mountains in southeast Tibet – Acta Prataculturae Sinica 27: 36-46 –


[ 张大才, 朱玉怀, 李双智 (2018). 东达山高寒草甸8种植物气孔特征沿土壤水分梯度的变化. 草业学报, 27,36-46.]

Zhang D. P. (1989) – Studies of stomata on the rice plant leaf blade. II. Dynamic morphogenesis of stomata under varied ecological conditions – Journal of Fujian Agricultural College 18(3): 302-307 – https://eurekamag.com/research/001/954/001954998.php – (On our blog : https://plantstomata.wordpress.com/2022/01/13/dynamic-morphogenesis-of-stomata-under-varied-ecological-conditions/ )

Zhang F.-P., Carins-Murphy M. R., Cardoso A. A., Jordan G. J., Brodribb T. J. (2018) – Similar geometric rules govern the distribution of veins and stomata in petals, sepals and leaves – New Phytologist – https://doi.org/10.1111/nph.15210 – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.15210?af=R – (On our blog : https://plantstomata.wordpress.com/2018/05/22/the-relationships-between-veins-stomata-and-epidermal-cells-in-leaves-sepals-and-petals/ )

Zhang G., Thompson A., Schisler D., Johnson E. T. (2019) – Characterization of the infection process by Peronospora belbahrii on basil by scanning electron microscopy – Heliyon 5(1): e01117 – https://doi.org/10.1016/j.heliyon.2019.e01117
https://www.sciencedirect.com/science/article/pii/S2405844018353829 – (On our blog : https://plantstomata.wordpress.com/2019/12/09/one-or-more-sporangiophores-grew-through-stomata-to-produce-new-sporangia-on-both-the-abaxial-and-adaxial-surfaces-of-leaves/ )

Zhang H. (2012) – Using soil drying as a regulative tool to enhance crop water use efficiency – Presentation at New Phytologist Symposium Nr. 29 on Stomata 2012 –https://www.newphytologist.org/app/webroot/img/upload/files/29thNPSAbstractBook.pdf – (On our blog : https://plantstomata.wordpress.com/2018/01/13/a-controlled-soil-drying-can-enhance-whole-plant-senescence-and-crop-water-use-efficiency/ )

Zhang H., Dong S., Wang M., Wang W., Song W., Dou X., Zheng X., Zhang Z. (2010) – The role of vacuolar processing enzyme (VPE) from Nicotiana benthamiana in the elicitor-triggered hypersensitive response and stomatal closure – J. Exp. Bot. 61: 3799–3812 – doi: 10.1093/jxb/erq189https://academic.oup.com/jxb/article/61/13/3799/534541 – (On our blog : https://plantstomata.wordpress.com/2020/09/10/vpe-functions-not-only-in-elicitor-induced-hr-but-also-in-elicitor-induced-stomatal-closure/ )

Zhang H., Fang Q., Zhang Z., Wang Y., Zheng X. (2009) – The role of respiratory burst oxidase homologues in elicitor-induced stomatal closure and hypersensitive response in Nicotiana benthamiana. – J. Exp. Bot. 60, 3109–3122. – doi: 10.1093/jxb/erp146 – https://www.ncbi.nlm.nih.gov/pubmed/19454596 – (On our blog : https://plantstomata.wordpress.com/2018/07/22/two-rboh-function-in-elicitor-induced-stomatal-closure-but-not-in-elicitor-induced-hr/ )

Zhang H., Pan C. Z., Gu S. H., Ma Q. M., Zhang Y. Q., Li X., Shi K. (2019) – Stomatal movements are involved in elevated CO2-mitigated high temperature stress in tomato – Physiol Plant. 165(3): 569–583 – doi:10.1111/ppl.12752 – https://onlinelibrary.wiley.com/doi/abs/10.1111/ppl.12752 – (On our blog : https://plantstomata.wordpress.com/2020/01/13/rboh1%e2%80%90dependent-h2o2-accumulation-was-involved-in-the-eco2%e2%80%90induced-stomatal-closure/ )

Zhang H., Wang X., Wang S. (2004) – A study on stomatal traits of Platanus acerifolia under urban stress – Journal of Fudan University  43: 651–656 – http://europepmc.org/abstract/cba/460789 – (On our blog : https://plantstomata.wordpress.com/2019/03/04/stomatal-density-and-stomatal-length-are-more-sensitive-and-available-to-indicate-urban-environmental-stress/ )

Zhang J., Davies W. J. (1986) – Chemical and hydraulic influences on the stomata of flooded plants – J. Exp. Bot. 37: 1479-1491 – https://doi.org/10.1093/jxb/37.10.1479https://academic.oup.com/jxb/article-abstract/37/10/1479/519902?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2020/06/10/nutrient-deficiency-may-limit-stomatal-opening-and-growth-in-flooded-plants/ )

Zhang J., Davies W. J. (1989) – Sequential responses of whole plant water relations towards prolonged soil drying and the mediation by xylem sap ABA concentrations in the regulation of stomatal behaviour of sunflower plants – New Phytol 113: 167–174 – DOI: 10.1111/j.1469-8137.1989.tb04703.x – https://www.jstor.org/stable/2556693?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2019/03/04/the-mediation-by-xylem-sap-aba-concentrations-in-the-regulation-of-stomatal-behaviour/ )

Zhang J., De‐Oliveira‐Ceciliato P., Takahashi Y., Schulze S., Dubeaux G., Hauser F., Azoulay‐Shemer T., Toldsepp K., Kollist H., Rappel W.- J., Schroeder J. I. (2018) – Insights into the molecular mechanisms of CO2‐mediated regulation of stomatal movements – Current Biology 28: R1356– R1363 – https://doi.org/10.1016/j.cub.2018.10.015https://www.cell.com/current-biology/fulltext/S0960-9822(18)31344-7?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0960982218313447%3Fshowall%3Dtrue#%20 – (On our blog : https://plantstomata.wordpress.com/2019/11/27/molecular-mechanisms-of-co2%e2%80%90mediated-regulation-of-stomatal-movements/ )

Zhang J., Pian R., Yang E., Zhou W., He Q., Chen X. (2020)In vitro induction and characterisation of tetraploid drumstick tree (Moringa oleifera Lam.) – Open Life Sciences – https://doi.org/10.1515/biol-2020-0087 -De Gruyter Open Access November 18, 2020 – https://www.degruyter.com/document/doi/10.1515/biol-2020-0087/html – (On our blog : https://plantstomata.wordpress.com/2022/04/07/the-tetraploid-of-moringa-exhibited-superior-agronomical-traits-improved-biomass-yield-and-significantly-enhanced-leaf-and-stomatal-size-than-diploids/ )

Zhang J., Schurr U., Davies W. J. (1987) – Control of stomatal behavior by abscisic acid which apparently originates in the roots – Journ. Exp. Bot. 38(6): 1174-1181 – Control of Stomatal Behaviour by Abscisic Acid which Apparently Originates in the Rootshttps://doi.org/10.1093/jxb/38.7.1174 – https://academic.oup.com/jxb/article-abstract/38/7/1174/440751?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2019/03/22/aba-can-move-from-the-roots-to-the-epidermis-and-restrict-stomatal-aperture/ )

Zhang J., Wang N., Miao Y., Hauser F., McCammon J. A., Rappel W.-J., Schroeder J. I. (2018) – Identification of SLAC1 anion channel residues required for CO2/bicarbonate sensing and regulation of stomatal movements – PNAS 115 (44): 11129-11137 – https://doi.org/10.1073/pnas.1807624115 – http://www.pnas.org/content/115/44/11129 –  (On our blog : https://plantstomata.wordpress.com/2018/11/01/slac1-anion-channel-residues-required-for-regulation-of-stomatal-movements/ )

Zhang J., Zhou H., Zhou M., Ge Z., Zhang F., Foyer C. H., Yuan X., Xie Y. (2020) – The coordination of guard-cell autonomous ABA synthesis and DES1 function in situ regulates plant water deficit responses – J Adv Res. 27: 191-197 – doi: 10.1016/j.jare.2020.07.013 – PMID: 33318877 – PMCID: PMC7728585 – https://pubmed.ncbi.nlm.nih.gov/33318877/ – (On our blog : https://plantstomata.wordpress.com/2022/03/14/the-coordinated-synthesis-of-aba-and-des1-expression-is-required-for-drought-induced-stomatal-closure/ )

Zhang J. H., Fu C., Kanzawa H. (2001) – Simulating canopy stomatal conductance of winter wheat and its distribution using remote sensing information – Journal of Environmental Sciences 13(4): 439-443 – (Article not found)

Zhang J.-Y., He S.-B., Li L., Yang H.-Q. (2014) – Auxin inhibits stomatal development through MONOPTEROS repression of a mobile peptide gene STOMAGEN in mesophyll – PNAS 111 (29) E3015-E3023 – doi:10.1073/pnas.1400542111 – http://www.pnas.org/content/111/29/E3015.full – (On our blog : https://plantstomata.wordpress.com/2018/01/20/auxin-signaling-in-mesophyll-to-coordinate-stomatal-development-with-photosynthesis/ )

Zhang L., Liu L., Zhao H., Jiang Z., Cai J., (2020) – Differences in Near Isohydric and Anisohydric Behavior of Contrasting Poplar Hybrids (I-101 (Populus alba L.) × 84K (Populus alba L. × Populus glandulosa Uyeki)) under Drought-Rehydration Treatments – Forests 11(4): 402- – https://doi.org/10.3390/f11040402https://www.mdpi.com/1999-4907/11/4/402 – (On our blog : https://plantstomata.wordpress.com/2021/12/06/the-trade-off-between-carbon-distribution-and-stomatal-regulation-should-be-considered-separately-within-genotypes-of-the-same-species/ )

Zhang L., Moran M. D., Brook J. R. (2001) – A comparison of models to estimate in-canopy photosynthetically active radiation and their influence on canopy stomatal resistance – Atmos. Environ. 35: 4463-4470 – DOI:10.1029/98JD01564

Zhang L., Niu H., Wang S., Li Y., Zhao X. (2010) – Effects of temperature increase and grazing on stomatal density and length of four alpine Kobresia meadow species, Qinghai-Tibetan Plateau – Acta Ecol. Sin. 30: 6961–6969 – http://en.cnki.com.cn/Article_en/CJFDTotal-STXB201024032.htm – (On our blog : https://plantstomata.wordpress.com/2019/03/04/effects-of-temperature-increase-and-grazing-on-stomatal-density-and-length/ )

Zhang L. R., Niu H. S., Wang S. P., Zhu X., Luo C., Li Y. N., Zhao X. Q. (2012) – Gene or environment? Species-specific control of stomatal density and length – Ecology and Evolution 2 (5): 1065–1070 – DOI: 10.1002/ece3.233 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399171/ – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/69825 )

Zhang L., Takahashi Y., Hsu P.-K., Kollist H., Merillo E., Krysan P. J., Schroeder J. I. (2020) – FRET kinase sensor development reveals SnRK2/OST1 activation by ABA but not by MeJA and high CO2 during stomatal closure – https://elifesciences.org/articles/56351 – (On our blog : https://plantstomata.wordpress.com/2021/01/28/stomatal-co2-signaling-requires-basal-aba-and-snrk2-signaling-but-not-snrk2-activation/ )

Zhang L., Wang S., Yang X., Cui X., Niu H. (2021) – An Intrinsic Geometric Constraint on Morphological Stomatal Traits – Front Plant Sci. 12: 658702 – doi: 10.3389/fpls.2021.658702 – PMID: 33968115 – PMCID: PMC8097139 – https://pubmed.ncbi.nlm.nih.gov/33968115/ – (On our blog : https://plantstomata.wordpress.com/2022/09/02/geometric-constraint-on-morphological-stomatal-traits/ )

Zhang R.-X., Ge S., He J., Li S., Hao Y., Du H., Liu Z., Cheng R., Feng Y.-Q., Xiong L., Li C., Hetherington A. M., Liang Y.-K. (2018) – BIG regulates stomatal immunity and jasmonate production in Arabidopsis -New Phytologist published online and citable – https://doi.org/10.1111/nph.15568 – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/nph.15568?af=R – (On our blog : https://plantstomata.wordpress.com/2018/10/30/big-negatively-and-positively-regulate-the-myc2%e2%80%90-and-erf1%e2%80%90-arms-of-the-ja-signalling-pathway-in-stomata/ )

Zhang S., Cai Z., Wang X. (2009) – The primary signaling outputs of brassinosteroids are regulated by abscisic acid signaling – PNAS 106(11): 4543-4548 – https://doi.org/10.1073/pnas.0900349106 – http://www.pnas.org/content/106/11/4543?ijkey=aa2f23b79d7deb06e9721fe8f74ed38c1bcb0bd6&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2018/09/12/the-molecular-mechanisms-by-which-brs-could-interact-with-aba/

Zhang S., Li Q., Ma K., Chen L., (2001) – Temperature-dependent gas exchange and stomatal/nonstomatal limitation to CO2 assimilation of Quercus liaotungensis under midday higher irradiance – Photosynthetica 39: 383-388 –

Zhang S.-B., Guan Z.-J., Chang W., Hu H., Yin Q,, Cao K.-F. (2011) – Slow photosynthetic induction and low photosynthesis in Paphiopedilum armeniacum are related to its lack of guard cell chloroplast and peculiar stomatal anatomy – Physiologia Plantarum 142: 118–127 – https://pdfs.semanticscholar.org/41b2/eb995324236f2d172d28f8d314a03d27b30d.pdf – (On our blog : https://plantstomata.wordpress.com/2018/09/07/evidence-for-the-morphological-and-physiological-evolution-of-stomata-relation-for-water-conservation-under-natural-selection/ )

Zhang S.-B., Guan Z.-J., Sun M., Zhang J.-J., Cao K.-F., Hu H. (2012) – Evolutionary Association of Stomatal Traits with Leaf Vein Density in Paphiopedilum, Orchidaceae – Plos One – https://doi.org/10.1371/journal.pone.0040080https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0040080 – (On our blog : https://plantstomata.wordpress.com/2020/02/24/evolutionary-association-of-stomatal-traits-with-leaf-vein-density/ )

Zhang S. Q., Outlaw W. H. Jr. (2001) – The guard‐cell apoplast as a site of abscisic acid accumulation in Vicia faba L. – Plant, Cell and Environment 24: 347–355 – https://doi.org/10.1046/j.1365-3040.2001.00677.x –https://onlinelibrary.wiley.com/doi/full/10.1046/j.1365-3040.2001.00677.x – (On our blog : https://plantstomata.wordpress.com/2019/03/04/stomata-will-display-higher-sensitivity-to-leaf-apoplastic-aba-if-stomata-are-widely-open-in-a-relatively-dry-atmosphere/ )

Zhang S. Q., Outlaw W. H. Jr. (2001) – Abscisic acid introduced into the transpiration stream accumulates in the guard-cell apoplast and causes stomatal closure – Plant, Cell and Environment 24: 1045-1054 – https://doi.org/10.1046/j.1365-3040.2001.00755.x – https://onlinelibrary.wiley.com/doi/full/10.1046/j.1365-3040.2001.00755.x – (On our blog : https://plantstomata.wordpress.com/2019/02/04/abscisic-acid-accumulates-in-the-guard-cell-apoplast-and-causes-stomatal-closure/ )

Zhang S. Q., Outlaw W. H. Jr. (2001) – Gradual long-term water stress results in abscisic acid accumulation in the guard-cell symplast and guard-cell apoplast of intact Vicia faba L. plants – J Plant Growth Regul 20: 300–307 – https://doi.org/10.1007/s003440010021https://library.vukrom.cz/documents/29345?back=https%3A%2F%2Flibrary.vukrom.cz%2Fauthorities%2F110336%3Flocale%3Dcs&group=36945,21202,29345,26415,36944,36630,36943,21257 – (On our blog : https://plantstomata.wordpress.com/2019/03/04/water-stress-results-in-aba-accumulation-in-the-stomatal-guard-cell-symplast-and-guard-cell-apoplast/ )

Zhang S. Q., Outlaw W. H. Jr., Aghoram K. (2001) – Relationship between changes in the guard cell abscisic acid content and other stress$related physiological parameters in intact plants – J. Exp. Bot. 52(355): 301-308 – https://watermark.silverchair.com/520301.pdf? – (On our blog : https://plantstomata.wordpress.com/2018/03/28/changes-in-the-guard-cell-aba-content-and-other-stress-related-physiological-parameters/ )

Zhang T., Chen S., Harmon A. C. (2014) – Protein phosphorylation in stomatal movement – Plant Signa. Behav. 9:e972845 – doi: 10.4161/ 15592316.2014.972845 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4622631/ – (On our blog : https://plantstomata.wordpress.com/2018/07/23/the-essential-role-of-protein-phosphorylation-in-aba-induced-stomatal-closure-and-in-blue-light-induced-stomatal-opening/ )

Zhang T.-Y., Li F.-C., Fan C.-M., Li X., Zhang F.-F., He J.-M. (2017) – Role and interrelationship of MEK1-MPK6 cascade, hydrogen peroxide and nitric oxide in darkness-induced stomatal closure – Plant Science 262: 190-199 – https://doi.org/10.1016/j.plantsci.2017.06.010https://www.sciencedirect.com/science/article/abs/pii/S0168945217301875?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2021/05/11/genetic-and-biochemical-evidences-not-only-show-that-mek1-mpk6-cascade-atrbohd-f-dependent-h2o2-and-nia1-dependent-no-are-all-involved-in-dark-induced-stomatal-closure/ )

Zhang W. (2011) – Roles of heterotrimeric G proteins in guard cell ion channel regulation – Plant Signal Behav. 6(7): 986-990 – doi: 10.4161/psb.6.7.15461 – PMID: 21617376 – PMCID: PMC3257774 – https://pubmed.ncbi.nlm.nih.gov/21617376/ – (On our blog : https://plantstomata.wordpress.com/2021/10/03/g-protein-regulation-of-ion-channels-on-the-plasma-membrane-of-stomatal-guard-cells/ )

Zhang W., Fan L. M., Wu W. H. (2007) – Osmo-sensitive and stretch-activated calcium-permeable channels in Vicia faba guard cells are regulated by actin dynamics – Plant Physiology 143: 1140–1151 – https://doi.org/10.1104/pp.106.091405http://www.plantphysiol.org/content/143/3/1140 – (On our blog : https://plantstomata.wordpress.com/2019/01/11/osmo-sensitive-and-stretch-activated-ca2-channels-stomata-and-their-regulation-by-osmotic-changes-and-actin-dynamics/ )

Zhang W., He J., Zhang L., He S. Y., Ryser E., Li H. (2019) – Stomata Facilitated Sorption of Silver Nanoparticles by Arabidopsis thaliana – Geophysical Research Abstracts Vol. 21, EGU2019-15061, 2019 – https://meetingorganizer.copernicus.org/EGU2019/EGU2019-15061.pdf – (On our blog : https://plantstomata.wordpress.com/2019/03/21/stomata-facilitated-sorption-of-silver-nanoparticles/ )

Zhang W., He S. Y., Assmann S. M. (2008) – The plant innate immunity response in stomatal guard cells invokes G-protein-dependent ion channel regulation – Plant J. 56: 984–996 – doi: 10.1111/j.1365-313X.2008.03657.x – https://www.ncbi.nlm.nih.gov/pubmed/18702674 – (On our blog : https://plantstomata.wordpress.com/2018/07/23/insights-into-the-elusive-signaling-process-underlying-pti-associated-stomatal-responses/ )

Zhang W., Jeon B. W., Assmann S. M. (2011) – Heterotrimeric G-protein regulation of ROS signaling and calcium currents in Arabidopsis guard cells – J. Exp. Bot. 62: 2371–2379 – doi: 10.1093/jxb/erq424 – https://www.ncbi.nlm.nih.gov/pubmed/21262908 – (On our blog : https://plantstomata.wordpress.com/2018/07/23/heterotrimeric-g-protein-regulation-of-ros-signaling-and-calcium-currents-in-stomata/ )

Zhang W., Nilson S. E., Assmann S. M. (2008) – Isolation and whole-cell patch clamping of Arabidopsis guard cell protoplasts – CSH Protoc. 2008: pdb prot5014 – doi: 10.1101/pdb.prot5014 – http://cshprotocols.cshlp.org/content/2008/6/pdb.prot5014.abstract – (On our blog : https://plantstomata.wordpress.com/2018/01/19/isolation-and-whole-cell-patch-clamping-of-guard-cell-protoplasts-stomata/ )

Zhang X., Dong F. C., Gao J. F., Song C. P. (2001) – Hydrogen peroxide- induced changes in intracellular pH of guard cells precede stomatal closure – Cell Res. 11: 37–43 – doi: 10.1038/sj.cr.7290064 – http://www.esalq.usp.br/lepse/imgs/conteudo_thumb/Hydrogen-peroxide-induced-changes-in-intracellular-pH-of-guard-cells-precede-stomatal-closure-1.pdf – (On our blog : https://plantstomata.wordpress.com/2018/07/23/h2o2-is-important-at-an-early-stage-in-the-signal-cascade-leading-to-stomatal-closure/ )

Zhang X., Mei X., Wang Y., Huang G., Feng F., Liu X., Guo R., Gu F., Hu X., Yang Z., Zhong X., Li Y. (2020) – Stomatal conductance bears no correlation with transpiration rate in wheat during their diurnal variation under high air humidity – PeerJ. 8: e8927 – DOI: 10.7717/peerj.8927https://peerj.com/articles/8927.pdf – (On our blog : https://plantstomata.wordpress.com/2021/02/19/stomatal-conductance-bears-no-correlation-with-transpiration-rate-under-high-air-humidity/ )

Zhang X., Miao Y. C., An G. Y., Zhou Y., Shangguan Z. P., Gao J. F., Song C. P. (2001) – K+ channels inhibited by hydrogen peroxide mediate abscisic acid signaling in guard cells – Cell Res. 11: 195–202 – DOI: 10.1038/sj.cr.7290086 – https://www.nature.com/articles/7290086 – (On our blog : https://plantstomata.wordpress.com/2019/03/04/h2o2-mediates-aba-induced-stomatal-movement-by-targeting-inward-k-channels-at-plasma-membrane/ )

Zhang X., Takemiya A., Kinoshita T., Shimazaki K. (2007) – Nitric oxide inhibits blue light-specific stomatal opening via abscisic acid signaling pathways in Vicia guard cells – Plant Cell Physiol. 48: 715-723 – https://academic.oup.com/pcp/article/48/5/715/2279068 – (On our blog : https://plantstomata.wordpress.com/2018/07/24/no-and-h-2-o-2-inhibit-blue-light-induced-activation-of-h-atpase-and-stimulate-stomatal-closure-by-aba/ )

Zhang X., Wang H., Takemiya A., Song C., Kinoshita T., Shimazaki K. (2004) – Inhibition of blue light-dependent H+ pumping by abscisic acid through hydrogen peroxide-induced dephosphorylation of the plasma membrane H+-ATPase in guard cell protoplasts – Plant Physiol. 136: 4150–4158 – DOI: 10.1104/pp.104.046573 – http://europepmc.org/abstract/MED/15563626 – (On our blog : https://plantstomata.wordpress.com/2018/03/23/inhibition-of-blue-light-dependent-h-pumping-by-aba-through-hydrogen-peroxide-induced-dephosphorylation-in-stomatal-protoplasts/ )

Zhang X., Yu C. M., An G. Y., Zhou Y., Shangguan Z. P., Gao J. F., Song C. P. (2001) – K+channels inhibited by hydrogen peroxide mediate abscisic acid signaling in Vicia guard cells – Cell Res. 11: 195–202 – DOI: 10.1038/sj.cr.7290086https://www.nature.com/articles/7290086.pdf?origin=ppub – (On our blog : https://plantstomata.wordpress.com/2019/05/28/h2o2-mediates-aba-induced-stomatal-movement-by-targeting-inward-k-channels-at-plasma-membrane-2/ )

Zhang X., Zhang L., An G. Y., Gao J. F., Song C. P. (2001) – Studies on ABA-induced H2O2 in Vicia guard cells by means of confocal laser scanning microscopy – Acta Biol Exp Sin 34(1): 71-76 – PMID: 12549013 – https://www.ncbi.nlm.nih.gov/pubmed/12549013 – (On our blog : https://plantstomata.wordpress.com/2019/05/28/h2o2-is-possibly-involved-in-aba-signaling-leading-to-stomatal-closure/ )

Zhang X., Zhang L., Dong F., Song C. P., Gao J., (2000) – Generation of hydrogen peroxide in abscisic acid signalling in stomatal guard cells of Vicia faba L. – Plant Biology (Rockville) : 38 – https://eurekamag.com/research/034/978/034978888.php

Zhang X., Zhang L., Dong F., Gao J., Galbraith D. W., Song C. P. (2001) – Hydrogen peroxide is involved in abscisic acid-induced stomatal closure in Vicia faba – Plant Physiol. 126: 1438–1448 – https://doi.org/10.1104/pp.126.4.1438 – http://www.plantphysiol.org/content/126/4/1438 – (On our blog : https://plantstomata.wordpress.com/2018/07/24/aba-may-close-the-stomata-via-a-pathway-with-h2o2-production-involved-and-h2o2-may-be-an-intermediate-in-aba-signaling/ )

Zhang X. Q., Wei P. C., Xiong Y. M., Yang Y., Chen J., Wang X. C. (2011) – Overexpression of the Arabidopsis α-expansin gene AtEXPA1 accelerates stomatal opening by decreasing the volumetric elastic modulus –Plant Cell Rep 30: 27–36 – doi: 10.1007/s00299-010-0937-2 – https://www.ncbi.nlm.nih.gov/pubmed/20976459?dopt=Abstract – (On our blog : https://plantstomata.wordpress.com/2018/12/03/the-putative-role-of-atexpa1-as-controller-of-stomatal-opening-rate-and-its-regulation/

Zhang X. Y., Wang H. M., Hou Z. D., Wang G. X. (2003) – Stomatal density and distributions of spring wheat leaves under different planting densities and soil moisture levels – Acta Phytoecologica Sinica 27: 133–136 – doi: 10.17521/cjpe.2003.0020 – http://www.plant-ecology.com/EN/10.17521/cjpe.2003.0020 – (On our blog : https://plantstomata.wordpress.com/2019/03/04/changes-in-stomatal-densities-and-distributions-are-the-result-of-different-water-conditions-induced-by-planting-densities/ )

Zhang Y., Bergmann D. C., Dong J. (2016) – Fine-scale dissection of the subdomains of polarity protein BASL in stomatal asymmetric cell division – J Exp Bot.(17): 5093-5103 – doi: 10.1093/jxb/erw274 – PMID: 27422992  – https://www.ncbi.nlm.nih.gov/pubmed/27422992 – (On our blog : https://plantstomata.wordpress.com/2018/10/05/basl-integrates-multiple-regulatory-inputs-to-provide-a-mechanism-that-promotes-difference-during-stomatal-lineage-acds/ )

Zhang Y., Guo X., Dong J. (2016) – Phosphorylation of the Polarity Protein BASL Differentiates Asymmetric Cell Fate through MAPKs and SPCH – Curr. Biol. 26(21): 2957-2965 – https://doi.org/10.1016/j.cub.2016.08.066https://www.cell.com/current-biology/fulltext/S0960-9822(16)31011-9 – (On our blog : https://plantstomata.wordpress.com/2021/12/05/basl-polarization-leads-to-elevated-nuclear-mpk6-signaling-and-lowered-spch-abundance-in-one-of-the-two-daughter-cells/ )

Zhang Y., Kaiser E., Li T., Marcelis L. F. M. (2021) –  Salt stress slows down dynamic photosynthesis mainly through osmotic effects on dynamic stomatal behavior – Authorea – June 02, 2021 – DOI: 10.22541/au.162264615.56315760/v1https://www.authorea.com/users/417597/articles/524631-salt-stress-slows-down-dynamic-photosynthesis-mainly-through-osmotic-effects-on-dynamic-stomatal-behavior – (On our blog : https://plantstomata.wordpress.com/2021/07/27/osmotic-effect-strongly-impacts-dynamic-stomatal-and-photosynthetic-behavior-under-salt-stress/ )

Yuqin Zhang, Himabindu Vasuki Kilambi, Jie Liu, Hamutal Bar, Shani Lazary, Aiman Egbaria, Dagmar Ripper, Laurence Charrier, Zeinu Mussa Belew, Nikolai Wulff, Suresh Damodaran, Hussam Hassan Nour-Eldin, Asaph Aharoni, Laura Ragni, Lucia Strader, Nir SadeRoy Weinstain, Markus Geisler, Eilon Shani, (2021) – ABA homeostasis and long-distance translocation are redundantly regulated by ABCG ABA importers – SCIENCE ADVANCES 7(43): – https://www.science.org/doi/10.1126/sciadv.abf6069 – (On our blog : https://plantstomata.wordpress.com/2021/11/11/abcg17-and-abcg18-double-knockdown-revealed-that-the-transporters-encoded-by-these-genes-not-only-limit-stomatal-aperture-size-conductance-and-transpiration/ )

Zhang Y., Lv S., Wang G. (2018) – Strigolactones are common regulators in induction of stomatal closure in planta – Plant Signal Behav. 13(3): e1444322 – doi: 10.1080/15592324.2018.1444322 – Epub 2018 Mar 13 – https://pubmed.ncbi.nlm.nih.gov/29473784/ – (On our blog : https://plantstomata.wordpress.com/2020/12/31/sls-could-serve-as-common-regulators-in-the-modulation-of-stomatal-apertures-of-various-plant-species/ )

Zhang Y.-J., Meinzer F. C., Qi J.-H., Goldstein G., Cao K.-F. (2013) – Midday stomatal conductance is more related to stemrather than leaf water status in subtropical deciduous andevergreen broadleaf trees – Plant, Cell and Environment  36: 149–158 – https://www.academia.edu/18598975/Midday_stomatal_conductance_is_more_related_to_stem_rather_than_leaf_water_status_in_subtropical_deciduous_and_evergreen_broadleaf_trees – (On our blog : https://plantstomata.wordpress.com/2022/01/07/99170/ )

Zhang Y., Novick K. A., Song C., Zhang Q., Hwang T. (2017) – Representation of physiological drought at ecosystem level based on model and eddy covariance measurements – American Geophysical Union, Fall Meeting 2017, abstract #B13H-1852 – https://ui.adsabs.harvard.edu/abs/2017AGUFM.B13H1852Z/abstract – (On our blog : https://plantstomata.wordpress.com/2022/09/05/a-phenomena-of-isohydricity-in-which-plants-tend-to-close-stomata-to-keep-the-leaf-water-potential-constant-and-reduce-the-risk-of-hydraulic-failure/ )

Zhang Y., Sun Y., Liu X., Deng J., Yao J., Zhang Y., Deng S., Zhang H., Zhao N., Li J., Zhou X., Zhao R., Chen S. (2021) Populus euphratica Apyrases Increase Drought Tolerance by Modulating Stomatal Aperture in Arabidopsis – Int. J. Mol. Sci. 22: 9892 – https://doi.org/10.3390/ ijms22189892file:///C:/Users/wille/Downloads/ijms-22-09892.pdf – (On our blog : https://plantstomata.wordpress.com/2022/02/21/a-speculative-model-of-apyrase-signaling-in-eatp-and-aba-regulated-stomatal-movements-under-drought/ )

Zhang Y., Wang P., Shao W., Zhu J. K., Dong J. (2015) -The BASL polarity protein controls a MAPK signaling feedback loop in asymmetric cell division – Dev Cell 33(2): 136-149 – https://doi.org/10.1016/j.devcel.2015.02.022

Zhang Y., Yang S. J., Sun M., Cao K. F. (2014) – Stomatal traits are evolutionarily associated with vein density in basal angiosperms – Plant Science Journal 32: 320-328 –


[ 张亚, 杨石建, 孙梅, 曹坤芳 (2014). 基部被子植物气孔性状与叶脉密度的关联进化. 植物科学学报, 32,320-328.]

Zhang Y., Zhu H., Zhang Q., Li M., Yan M., Wang R., Wang L., Welti R., Zhang W., Wang X. (2009) – Phospholipase Dα1 and phosphatidic acid regulate NADPH oxidase activity and production of reactive oxygen species in ABA-mediated stomatal closure in Arabidopsis – Plant Cell 21, 2357–2377 – doi: 10.1105/tpc.108.062992 – http://www.plantcell.org/content/early/2009/08/18/tpc.108.062992 – (On our blog : https://plantstomata.wordpress.com/2018/07/25/the-role-of-pld%ce%b11-and-pa-in-aba-induced-production-of-ros-in-stomata/ )

Zhang Y.-J., Meinzer F. C., Qi J.-H. et al (2013) – Midday stomatal conductance is more related to stem rather than leaf water status in subtropical deciduous and evergreen broadleaf trees – Plant Cell Environ 36: 149–158 –  https://doi.org/10.1111/j.1365-3040.2012.02563.x – https://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-3040.2012.02563.x – (On our blog : https://plantstomata.wordpress.com/2019/03/04/the-functional-significance-of-stomatal-regulation-in-broadleaf-tree-species-is-probably-for-preventing-stem-xylem-dysfunction/ )

Zhang Y. P., Wang Z. M., Wu Y. C., Zhang X. (2006) – Stomatal characteristics of different green organs in wheat under different irrigation regimes – Acta Agronomica Sinica 32: 70–75 – http://agris.fao.org/agris-search/search.do?recordID=CN2006001624 – (On our blog : https://plantstomata.wordpress.com/2019/03/05/stomatal-characteristics-of-different-green-organs-under-different-irrigation-regimes/ )

Zhang Z. F., Liu J. H., Fu X. F., et al (2017) – Effect of drought stress on stomata and ultrastructure of mesophyll cells of oat leaf – Journal of Triticeae Crops 37(9): 1216-1223 – http://d.old.wanfangdata.com.cn/Periodical/mlzwxb201709012

Zhang Z. Z., Zhao P., McCarthy H. R., Zhao X. H., Niu J. F., Zhu L. W., Ni G. Y., Ouyang L., Huang Y. Q. (2016) – Influence of the decoupling degree on the estimation of canopy stomatal conductance for two broadleaf tree species – Agricultural and Forest Meteorology 221: 230-241 – ISSN : 0168-1923 – doi: 10.1016/j.agrformet.2016.02.018https://www.infona.pl/resource/bwmeta1.element.elsevier-425c99c5-3f19-3a53-937b-e9947c3316cc – (On our blog : https://plantstomata.wordpress.com/2022/02/28/some-light-on-the-prediction-error-of-stomatal-conductance-derived-from-the-simplified-equation-in-different-forest-types/ )

Zhao C. (2019) – A conserved chloroplast retrograde signal regulates stomatal closure for drought tolerance in plants – https://researchdirect.westernsydney.edu.au/islandora/object/uws%3A51886 – (On our blog : https://plantstomata.wordpress.com/2022/05/13/mechanisms-from-both-physiological-and-molecular-aspects-of-a-chloroplast-retrograde-signal-that-enhances-plant-drought-tolerance-by-regulating-stomatal-closure/ )

Zhao C., Cai S., Wang Y., Chen Z. H. (2016) – Loss of nitrate reductases NIA1 and NIA2 impairs stomatal closure by altering genes of core ABA signalling components in Arabidopsis – Plant signalling & behavior 11(6): e1183088

Zhao C., Chavan S., He X., Zhou M., Cazzonelli C. I., Chen Z.-H., Tissue D. T., Ghannoum O. (2020) – Smart Film Impacts Stomatal Sensitivity of Greenhouse Capsicum Through Altered Light – biorxiv – doi: https://doi.org/10.1101/2020.09.22.309427https://www.biorxiv.org/content/10.1101/2020.09.22.309427v1.full – (On our blog : https://plantstomata.wordpress.com/2021/03/27/sg-upregulated-the-expression-of-key-genes-involved-in-stomatal-regulation-and-light-sensing/ )

Zhao C., Haigh A. M., Holford P., Chen Z. H. (2018) – Roles of Chloroplast Retrograde Signals and Ion Transport in Plant Drought Tolerance – International Journal of Molecular Sciences 19(4): 963 –

Zhao C., Wang Y. Y., Chan K. X., Chen G., Holford P., Haigh A. M., Chen Z. H. ( ) – Chloroplastretrograde Signal PAP bypasses Open Stomatal 1 to rescue gene expression of critical ABA signalling elements in guard cells and mesophyll cells of Arabidopsis –

Zhao C., Wang Y., Chan K. X., Marchant D. B., Franks P. J., Randall D., Tee E. E., Chen G., Ramesh S., Phua S. Y., Zhang B., Hills A., Dai F., Xye D., Gilliham M., Tyerman S., Nevo E., Wu F., Zhang G., Wong G. K.-S., Leebens-Mack J. H., Melkonian M., Blatt M. R., Soltis P. S., Soltis D. E., Pogson B. J., Chen Z.-H. (2019) – Evolution of chloroplast retrograde signaling facilitates green plant adaptation to land – PNAS 116 (11) 5015-5020 – https://doi.org/10.1073/pnas.1812092116https://www.pnas.org/content/116/11/5015 – (On our blog : https://plantstomata.wordpress.com/2019/04/02/pap-regulates-stomatal-closure-via-secondary-messengers-and-ion-transport-in-guard-cells/ )

Zhao L. , Sack F. D. (1999) –  Ultrastructure of stomatal development in Arabidopsis (Brassicaceae) leaves. – Amer. J. Botany 86: 929-939 – http://www.amjbot.org/content/86/7/929.full – (On our blog : https://plantstomata.wordpress.com/2018/01/29/ultrastructure-of-stomatal-development-2/ )

Zhao L., Wang L., Li J., Bai G., Shi Y., Ge Y. (2021) – Toward accurate estimating of crop leaf stomatal conductance combining thermal IR imaging, weather variables, and machine learning – Proceedings Volume 11747, Autonomous Air and Ground Sensing Systems for Agricultural Optimization and Phenotyping VI; 117470L – https://doi.org/10.1117/12.2587577
Event: SPIE Defense + Commercial Sensing, 2021, Online Only – https://www.spiedigitallibrary.org/conference-proceedings-of-spie/11747/117470L/Toward-accurate-estimating-of-crop-leaf-stomatal-conductance-combining-thermal/10.1117/12.2587577.short?SSO=1 – (On our blog : https://plantstomata.wordpress.com/2021/11/29/estimating-of-crop-leaf-stomatal-conductance-combining-thermal-ir-imaging-weather-variables-and-machine-learning/ )

Zhao P.-X., Miao Z.-Q., Zhang J., Chen S.-Y., Liu Q.-Q, Xiang C.-B. (2020) – Arabidopsis MADS-box factor AGL16 negatively regulates drought resistance via stomatal density and stomatal movement – Journal of Experimental Botany 71(19): 6092–6106 –
doi:10.1093/jxb/eraa303 – (On our blog : https://plantstomata.wordpress.com/2022/04/07/agl16-acts-as-a-negative-regulator-of-drought-resistance-by-modulating-leaf-stomatal-density-and-aba-accumulation/ )

Zhao R., Dielen V., Kinet J.-M., Boutry M. (2000) – Cosuppression of a plasma membrane H+-ATPaseisoform impairs sucrose translocation, stomatal opening, plant growth, and male fertility – Plant Cell. 12: 535–546 – PMCID: PMC139851 – PMID: 10760242 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139851/ – (On our blog : https://plantstomata.wordpress.com/2019/05/28/cosuppression-of-pma4-affected-the-guard-cells-stomatal-opening-and-photosynthesis-in-mature-leaves/ )

Zhao R. X., Zhang Q. B., Wu X. Y., Wang Y. (2001) – The effects of drought on epidermal cells and stomatal density of wheat leaves. Inner Mongolia Agricultural Science and Technology 6: 6–7 – 

Zhao S., Chen W., Ma D., Zhao F. (2006) – Influence of different salt level on stomatal character in rice leaves – Reclaiming and Rice Cultivation 6: 26–29 – http://en.cnki.com.cn/Article_en/CJFDTOTAL-KZDZ200606012.htm – (On our blog : https://plantstomata.wordpress.com/2019/03/05/different-salt-levels-and-stomatal-characters/ )

Zhao S., Jiang Y., Zhao Y., Huang S., Yuan M., Zhao Y., Guo Y. (2016) – CASEIN KINASE1-LIKE PROTEIN2 Regulates Actin Filament Stability and Stomatal Closure via Phosphorylation of Actin Depolymerizing Factor – Plant Cell – https://doi.org/10.1105/tpc.16.00078http://www.plantcell.org/content/28/6/1422?utm_source=TrendMD&utm_medium=cpc&utm_campaign=Plant_Cell_TrendMD_0 – (On our blog : https://plantstomata.wordpress.com/2020/01/15/ckl2-regulates-actin-filament-reorganization-and-stomatal-closure-mainly-through-phosphorylation-of-adf/ )

Zhao W., Fu P., Liu G., Zhao P. (2020) – Difference between emergent aquatic and terrestrial monocotyledonous herbs in relation to the coordination of leaf stomata with vein traits – AoB Plants 12(5): plaa047 – doi: 10.1093/aobpla/plaa047 – PMID: 33376587 – PMCID: PMC7750939 – https://pubmed.ncbi.nlm.nih.gov/33376587/ – (On our blog : https://plantstomata.wordpress.com/2021/04/24/the-differences-in-water-supply-between-emergent-aquatic-and-terrestrial-plants-modify-the-coordination-of-their-leaf-veins-and-stomatal-traits/ )

Zhao W., Liu B., Chang X., Yang Q., Yang Y., Liu Z., Cleverly J., Eamus D. (2016) – Evapotranspiration partitioning, stomatal conductance, and components of the water balance: A special case of a desert ecosystem in China – J. Hydrol. 538: 374–386 – https://doi.org/10.1016/j.jhydrol.2016.04.042https://www.sciencedirect.com/science/article/abs/pii/S0022169416302335?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2022/04/20/the-role-of-stomatal-regulation-of-canopy-transpiration-tc-as-a-determinant-of-ecosystem-water-balance/ )

Zhao W., Sun Y., Kjelgren R., Liu X. (2015) – Response of Stomatal Density and Bound Gas Exchange in Leaves of Maize to Soil Water Deficit – Plants, Soils, and Climate Faculty Publications. Paper 732 –  http://digitalcommons.usu.edu/psc_facpub/732 – https://digitalcommons.usu.edu/cgi/viewcontent.cgi?article=1731&context=psc_facpub – (On our blog : https://plantstomata.wordpress.com/2018/02/04/response-of-stomatal-density-and-bound-gas-exchange-to-soil-water-deficit/ )

Zhao W.-L., Chen Y.-J., Brodribb T. J., Cao K.-F. (2016) – Weak co-ordination between vein and stomatal densities in 105 angiosperm tree species along altitudinal gradients in Southwest China – Functional Plant Biology – http://dx.doi.org/10.1071/FP16012http://www.brodribblab.org.au/wp-content/uploads/2016/11/Weak-co-ordination.pdf – (On our blog : https://plantstomata.wordpress.com/2020/05/09/weak-co-ordination-between-vein-and-stomatal-densities/ )

Zhao W. L., Siddiq Z., Fu P. L., Zhang J. L., Cao K. F. (2017) – Stable stomatal number per minor vein length indicates the coordination between leaf water supply and demand in three leguminous species – Scientific reports 7: 2211 –

Zhao X., Li Y. Y., Xiao H. L., Xu C. S., Zhang, X. (2013) – Nitric oxide blocks blue light-induced K+ influx by elevating the cytosolic Ca2+ concentration in Vicia faba guard cells – J. Integr. Plant Biol. 55: 527–536 – doi: 10.1111/jipb.12038 – https://www.ncbi.nlm.nih.gov/pubmed/23384172 – (On our blog : https://plantstomata.wordpress.com/2018/07/25/ca2-plays-dual-and-distinctive-roles-in-the-crosstalk-between-bl-and-no-signaling-in-stomata-2/ )

Zhao X., Zhao M., Xiao J. T., Zhang W. X., Guan D., Wang M. Y., Li J. N., Zhang N. (2003) – Stomata characteristics of leaves of high-photosynthetic efficiency progenies from a cross between Oryza sativa and O. rufipogon and their parents – Acta Agronomica Sinica 29(2): 216-221 – https://eurekamag.com/research/004/328/004328511.php – (On our blog : https://plantstomata.wordpress.com/2019/02/01/stomata-characteristics-of-progenies-from-a-cross-between-oryza-sativa-and-o-rufipogon-and-their-parents/ )

Zhao X., Wang Y.-J., Wang Y.-L., Wang X.-L., Zhang X. (2011) –  Extracellular Ca2+ alleviates NaCl–induced stomatal opening through a pathway involving H2O2-blocked Na+ influx in Vicia guard cells – J. Plant Physiol. 168: 903-910 – PMID:21367483 – http://dx.doi.org/10.1016/j.jplph.2010.11.024http://www.sciencedirect.com/science/article/pii/S0176161711000630 – (On our blog : https://plantstomata.wordpress.com/2017/09/30/extracellular-ca2-alleviates-nacl-induced-stomatal-opening/ )

Zhao X., Yang Y., Shen, Z., Zhang H., Wang G., Gan Y. (2006) – Stomatal clustering in Cinnamomum camphora – South African Journal of Botany 72: 565-569 – https://doi.org/10.1016/j.sajb.2006.03.006 – https://www.sciencedirect.com/science/article/pii/S0254629906000883 – (On our blog : https://plantstomata.wordpress.com/2018/03/19/stomatal-clusters-are-probably-able-to-assist-in-water-conservation/ )

Zhao Y. (2019) – Researchers reveal factor in subtropical plant photosynthesis – CGTN – Plant 2019-12-23 – https://news.cgtn.com/news/2019-12-23/Researchers-reveal-factor-in-subtropical-plant-photosynthesis-MEswOHB6EM/index.html – (On our blog : https://plantstomata.wordpress.com/2019/12/23/82502/ )

Zhao Y., Chan Z., Gao J., Xing L., Cao M., Yu C., Hu Y., You J., Shi H., Zhu Y., Gong Y., Mu Z., Wang H., Deng X., Wang P., Bressan R. A., Zhu J.-K., (2016) – ABA receptor PYL9 promotes drought resistance and leaf senescence – PNAS 113(7): 1949-1954 – https://doi.org/10.1073/pnas.1522840113https://www.pnas.org/content/113/7/1949 – (On our blog: https://plantstomata.wordpress.com/2021/12/23/the-molecular-mechanism-of-aba-induced-leaf-senescence-and-an-important-role-of-pyl9-and-leaf-senescence-in-promoting-resistance-to-extreme-drought-stress/ )

Zhao Y., Zhao S., Mao T., Qu X., Cao W., Zhang L., Zhang W., He L., Li S., Ren S., Zhao J., Zhu G., Huang S., Ye K., Yuan,M., Guo Y. (2011) – The plant-specific actin binding protein SCAB1 stabilizes actin filaments and regulates stomatal movement in Arabidopsis – Plant Cell 23: 2314-2330 – https://doi.org/10.1105/tpc.111.086546http://www.plantcell.org/content/23/6/2314 – (On our blog : https://plantstomata.wordpress.com/2019/03/05/scab1-is-required-for-the-precise-regulation-of-actin-filament-reorganization-during-stomatal-closure/ )

Zhao Y. Y., Lyu M. A., Miao F., Chen G., Zhu X. G. (2022) – The evolution of stomatal traits along the trajectory toward C4 photosynthesis – Plant Physiol. 190(1): 441-458 – doi: 10.1093/plphys/kiac252 – PMID: 35652758 – https://pubmed.ncbi.nlm.nih.gov/24860185/ – (On our blog : https://plantstomata.wordpress.com/2022/09/13/insights-into-the-pattern-mechanism-and-role-of-stomatal-evolution-along-the-road-toward-c4/ )

Zhao Z. (2011)Arabidopsis Stomatal Opening and Closing Experiment – Bio-101: e74 – DOI: 10.21769/BioProtoc.74https://bio-protocol.org/bio101/e74 – (On our blog : https://plantstomata.wordpress.com/2020/12/07/how-to-measure-stomatal-apertures-following-aba-treatment/ )

Zhao Z., Assmann S. M. (2011) – The glycolytic enzyme, phosphoglycerate mutase, has critical roles in stomatal movement, vegetative growth, and pollen production in Arabidopsis thaliana –  J. Exp. Bot. 62: 5179–5189 – doi: 10.1093/jxb/err223 – https://www.ncbi.nlm.nih.gov/pubmed/21813794 – (On our blog : https://plantstomata.wordpress.com/2018/07/25/ipgams-and-glycolytic-activity-are-critical-for-stomatal-function-and-fertility/

Zhao Z., Stanley B. A., Zhang W., Assmann S. M. (2010) – ABA-Regulated G Protein Signaling in Arabidopsis Guard Cells: A Proteomic Perspective – J. Proteome Res. 9(4): 1637–1647 – DOI10.1021/pr901011h – http://pubs.acs.org/doi/abs/10.1021/pr901011h – (On our blog : https://plantstomata.wordpress.com/2018/01/17/aba-regulated-g-protein-signaling-in-stomata/ )

Zhao Z. X., Zhang W., Stanley B. A., Assmann S. M. (2008) – Functional proteomics of Arabidopsis thaliana guard cells uncovers new stomatal signaling pathways – Plant Cell 20: 3210–3226 – doi: 10.1105/tpc.108.063263 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2630442/ – (On our blog : https://plantstomata.wordpress.com/2018/07/26/functional-proteomics-uncovers-new-stomatal-signaling-pathways/ )

Zheng F.-Y., Peng S.-L., Zhao P. (2001) – Changes in Stomatal Density and Intrinsic Water Use Efficiency of Two Trema Species over the Last Century – Chin J Plan Ecolo  25(4): 405-409 – https://www.plant-ecology.com/EN/abstract/abstract6944.shtml – (On our blog : https://plantstomata.wordpress.com/2022/03/04/stomatal-densities-declining-and-water-use-efficiency-increasing-with-time/ )

Zheng L., Van Labeke M. C. (2017) – Long-Term Effects of Red- and Blue-Light Emitting Diodes on Leaf Anatomy and Photosynthetic Efficiency of Three Ornamental Pot Plants – Frontiers in Plant Science 8: 917- DOI: 10.3389/fpls.2017.00917https://europepmc.org/article/med/28611818 – (On our blog : https://plantstomata.wordpress.com/2020/03/05/long-term-effects-of-red-and-blue-light-on-stomata/ )

Zheng S-X., Shangguan Z.-P. (2005) – Relationship between stomata parameters of plants and atmospheric CO2 concentration change – Ecological Science 24(3): 264-267 – http://journal15.magtechjournal.com/Jwk_stkx/EN/abstract/abstract856.shtml# – (On our blog : https://plantstomata.wordpress.com/2022/02/18/the-progress-of-plant-stomata-parameters-in-the-reconstruction-of-the-palaeo-atmospheric-co2-concentration/ )

Zheng S-X., Shangguan Z.-P., Xue Q-W. (2006) – Changes of stomatal parameters of four typical species in the Loess Plateau of China over the last century – Acta Agriculturae Scandinavica, Section B – Soil & Pl.Sci. 56: 284-291 – https://doi.org/10.1080/09064710500321532https://www.tandfonline.com/doi/abs/10.1080/09064710500321532 – (On our blog : https://plantstomata.wordpress.com/2019/05/25/changes-of-stomatal-parameters-over-the-last-century/ )

Zheng T. C., Zhang X. K., Yin G. H., Wang L. N., Han Y. L., Chen L., Huang F., Tang J. W., Xia X. C., He Z. H. (2011) – Genetic gains in grain yield, net photosynthesis and stomatal conductance achieved in Henan Province of China between 1981 and 2008 – Field Crops Research 122: 225–233 – https://doi.org/10.1016/j.fcr.2011.03.015https://www.sciencedirect.com/science/article/abs/pii/S0378429011000979?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2020/06/23/genetic-gains-in-stomatal-conductance/ )

Zheng W., Jiang Y., Wang X., Huang S., Yuan M., Guo Y. (2019) – AP3M harbors actin filament binding activity that is crucial for vacuole morphology and stomatal closure in Arabidopsis – Proc. Natl. Acad. Sci. U.S.A. 116: 18132–18141 – doi: 10.1073/pnas.1901431116https://www.pnas.org/content/116/36/18132 – (On our blog : https://plantstomata.wordpress.com/2021/12/04/the-f-actin-binding-activity-of-ap3m-is-required-for-the-regulation-of-vacuole-morphology-in-guard-cells-during-stomatal-closure/ )

Zheng X., Kang S., Jing Y., Ren Z., Li L., Zhou J. -M., Berkowitz G., Shi J., Fu A., Lan W., Zhao F. Luan S. (2018) – Danger-Associated Peptides Close Stomata by OST1-Independent Activation of Anion Channels in Guard Cells – The Plant Cell 30 (5): 1132-1146 – DOI: 10.1105/tpc.17.00701 – http://www.plantcell.org/content/30/5/1132 – (On our blog : https://plantstomata.wordpress.com/2018/06/10/a-damp-triggered-signaling-pathway-triggers-stomata-immunity-through-an-ost1-independent-mechanism/

Zheng Y., Xu M., Hou R., Shen R., Qiu S., Ouyang Z. (2013) – Effects of experimental warming on stomatal traits in leaves of maize (Zea may L.) – Ecol. Evol. 3: 3095–3110 – doi: 10.1002/ece3.674 – https://onlinelibrary.wiley.com/doi/abs/10.1002/ece3.674 – (On our blog : https://plantstomata.wordpress.com/2018/10/15/effects-of-experimental-warming-on-stomatal-traits-2/ )

Zheng Y. P., Ming X. U., Wang J. S., Qin S., Wang H. X. (2015) – Responses of the stomatal traits and gas exchange of Maize leaves to climate warming – Acta Agron. Sin. 41: 601 – DOI: 10.3724/SP.J.1006.2015.00601https://www.researchgate.net/publication/289983261_Responses_of_the_Stomatal_Traits_and_Gas_Exchange_of_Maize_Leaves_to_Climate_Warming – (On our blog :

Zheng Z. L., Nafisi M., Tam A., Li H., Crowell D. N., Chary S. N., Schroeder J. I., Shen J., Yang Z. (2002) – Plasma membrane-associated ROP10 small GTPase is a specific negative regulator of abscisic acid responses in Arabidopsis – Plant Cell 14(11): 2787-2797 – PMID: 12417701 – PMCID: PMC152727 – https://www.ncbi.nlm.nih.gov/pubmed/12417701 – (On our blog : https://plantstomata.wordpress.com/2018/07/26/rop10-a-pm-localized-signaling-molecule-involved-in-the-negative-regulation-of-aba-signaling-in-stomata/ )

Zhengmin H., Tongming Y. (1998) – The relationship between the resistance of poplar to Marssonina brunnea and size and density of stomata and peroxidase activity – Journal of Nanjing Forestry University 22(4): 91-94 – https://eurekamag.com/research/003/313/003313244.php – (On our blog : https://plantstomata.wordpress.com/2022/01/08/no-relationship-between-resistance-and-the-size-and-density-of-stomata-or-the-transpiration-rate/ )

Zhenzhu X., Guangsheng Z. (2008) – Responses of leaf stomatal density to water status and its relationship with photosynthesis in a grass – Journal of Experimental Botany 59 (12): 3317-3325 – https://doi.org/10.1093/jxb/ern185https://academic.oup.com/jxb/article/59/12/3317/627451 – (On our blog : https://plantstomata.wordpress.com/2020/02/25/high-flexibilities-in-stomatal-density-and-guard-cell-size-will-change-in-response-to-water-status/ )

Zhong M. (2010) – Plant Vacuoles and the Regulation of Stomatal Opening – Nature Education 3(9): 45 – https://www.nature.com/scitable/topicpage/plant-vacuoles-and-the-regulation-of-stomatal-14163334/ – (On our blog : https://plantstomata.wordpress.com/2021/03/21/key-regulators-of-stomata-are-plant-vacuoles-fluid-filled-organelles-bound-by-a-single-membrane-called-the-tonoplast/ )

Zhong M., Cerabolini B. E. L., Castro-Diez P., Puyravaud J.-P., Cornelissen J. H. C. (2020) – Allometric co-variation of xylem and stomata across diverse woody seedlings – Plant, Cell & Environment ( IF 6.362 ) – DOI: 10.1111/pce.13826https://www.x-mol.com/paper/1273038415424155648 – (On our blog : https://plantstomata.wordpress.com/2021/01/25/allometric-co-variation-of-xylem-and-stomata)

Zhou N., Wang Y., Ya L., Porter A., Kürschner W. M., Li L., Lu N., McElwain J. C. (2019) – An inter-comparison study of three stomatal-proxy methods for CO2 reconstruction applied to early Jurassic Ginkgoales plants – Palaeogeography Palaeoclimatology Palaeoecology 109547 – DOI: 10.1016/j.palaeo.2019.109547https://www.sciencedirect.com/science/article/abs/pii/S0031018219304183?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2019/12/30/a-likely-occurrence-of-polyploidy-in-sphenobaiera-huangii-may-result-in-underestimated-paleo-co2-when-applying-mechanistic-method-due-to-an-increase-in-the-size-of-the-stomatal-complex/ )

Zhou S., Duursma R. A., Medlyn B. E., Kelly J. W. G., Prentice I. C. (2013) – How should we model plant responses to drought? An analysis of stomatal and non-stomatal responses to water stress – Agricultural and forest meteorology 182-183: 204-214 – DOI: 10.1016/j.agrformet.2013.05.009http://www.researchonline.mq.edu.au/vital/access/manager/Repository/mq:28087;jsessionid=F5E8393B52B58BBF6E4EBAA5E20A0755f0=sm_subject%3A%22Photosynthetic+limitation%22 – (On our blog : https://plantstomata.wordpress.com/2022/03/01/stomatal-and-non-stomatal-limitations-to-photosynthesis-must-both-be-considered-for-the-short-term-response-to-drought/ )

Zhou S., Medlyn B., Sabaté S., Sperlich D., Prentice I. C. (2014) – Short‐term water stress impacts on stomatal, mesophyll and biochemical limitations to photosynthesis differ consistently among tree species from contrasting climates – Tree Physiol 34: 1035–1046 – doi: 10.1093/treephys/tpu072. Epub 2014 Sep 4https://www.ncbi.nlm.nih.gov/pubmed/25192884 – (On our blog : https://plantstomata.wordpress.com/2019/03/05/adaptive-interspecific-differences-in-drought-responses-stomatal-mesophyll-and-biochemical-limitations-to-photosynthesis/ )

Zhou S.-X., Prentice I. C., Medlyn B. E. (2019) – Bridging Drought Experiment and Modeling: Representing the Differential Sensitivities of Leaf Gas Exchange to Drought – Front. Plant Sci., 15 January 2019 – https://doi.org/10.3389/fpls.2018.01965https://www.frontiersin.org/articles/10.3389/fpls.2018.01965/full – (On our blog : https://plantstomata.wordpress.com/2020/01/09/how-experimentally-derived-quantitative-information-can-improve-the-representation-of-stomatal-and-non-stomatal-photosynthetic-responses-to-drought-in-large-scale-vegetation-models/ )

Zhou S.-X., Prentice I. C., Medlyn B. E., Sabaté S. (2013) – Evidence-based modelling of diverse plant water use strategies on stomatal and non-stomatal components under drought – American Geophysical Union, Fall Meeting 2013, abstract id. B53C-0480 – https://ui.adsabs.harvard.edu/abs/2013AGUFM.B53C0480Z/abstract – (On our blog : https://plantstomata.wordpress.com/2022/03/12/water-use-strategies-and-stomatal-and-non-stomatal-components-under-drought/ )

Zhou Y., Vroegop-Vos I., Schuurink R. C., Pieterse C. M. J. , Van Wees S. C. M. (2017) – Atmospheric CO2 Alters Resistance of Arabidopsis to Pseudomonas syringae by Affecting Abscisic Acid Accumulation and Stomatal Responsiveness to Coronatine – Front. Plant Sci., 16 May 2017 – https://doi.org/10.3389/fpls.2017.00700 –https://www.frontiersin.org/articles/10.3389/fpls.2017.00700/full – (On our blog : https://plantstomata.wordpress.com/2017/10/29/co2-aba-accumulation-and-stomatal-responsiveness-to-coronatine/ )

Zhou X. F., Jin Y. H., Yoo C. Y., Lin X.-L., Kim W.-Y., Yun D.-J., Bressan R. A.,  Hasegawa P. M., Jin J. B. (2013) – CYCLIN H;1 regulates drought stress responses and blue light-induced stomatal opening by inhibiting reactive oxygen species accumulation in Arabidopsis – Plant Physiol. 162: 1030–1041  –http://chemport.cas.org/cgi-bin/sdcgi?APP=ftslink&action=reflink&origin=npg&version=1.0&coi=1:CAS:528:DC%2BC3sXps1OqsLo%3D&md5=9148d023de1dca6c9f9e0f7c9e793052 – (https://plantstomata.wordpress.com/2016/12/07/cych1-regulates-blue-light-mediated-stomatal-opening-by-controlling-reactive-oxygen-species-homeostasis/ )

Zhou X. M., Wu W. H., Yuan M., Wang X. C. (1999) – Regulation of the inward K+ -channels in stomatal guard cells by cytoskeletal microtubules – Chinese Science Bulletin 44: 919–923 –

Zhou Y. M., Han S. J. (2005) – Photosynthetic response and stomatal behaviour of Pinus koraiensis during the fourth year of exposure to elevated CO2 concentration – Photosynthetica 43: 445-449 – https://doi.org/10.1007/s11099-005-0071-5https://link.springer.com/article/10.1007/s11099-005-0071-5 – (On our blog : https://plantstomata.wordpress.com/2019/03/05/photosynthetic-response-and-stomatal-behaviour-during-the-fourth-year-of-exposure-to-elevated-co2-concentration/ )

Zhou Z., Lau O. S. (2021) – Dissecting the developmental roles of Pol II-associated proteins through the stomatal pores – New Phytol. 230: 11-13 – https://doi.org/10.1111/nph.17157https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.17157 – (On our blog : https://plantstomata.wordpress.com/2021/12/02/the-developmental-roles-of-pol-ii-associated-proteins-through-the-stomatal-pores/ )

Zhou Z., Wu Y., Yang Y., Du M., Zhang X., Guo Y., Li C., Zhou J.-M. (2015) – An Arabidopsis plasma membrane proton ATPase modulates JA signaling and is exploited by the Pseudomonas syringae effector protein AvrB for stomatal invasion – Plant Cell 27: 2032–2041 – doi: 10.1105/tpc.15.00466https://academic.oup.com/plcell/article/27/7/2032/6096642 – (On our blog : https://plantstomata.wordpress.com/2021/11/09/a-previously-unknown-pathway-exploited-by-pseudomonas-syringae-that-acts-upstream-of-coi1-to-regulate-ja-signaling-and-stomatal-opening/ )

Zhu J., Park J.-H., Lee S., Lee J. H., Hwang D., Kwak J. M., Kim Y. J. (2020) – Regulation of stomatal development by stomatal lineage miRNAs – PNAS 117(11): 6237-6245 – https://doi.org/10.1073/pnas.1919722117https://www.pnas.org/content/117/11/6237 – (On our blog : https://plantstomata.wordpress.com/2020/04/08/84012/ )

Zhu J., Talbott L. D., Jin X., Zeiger E. (1998) – The stomatal response to CO2 is linked to changes in guard cell zeaxanthin – Plant Cell Environment 21: 813-820 – https://doi.org/10.1046/j.1365-3040.1998.00323.x –https://onlinelibrary.wiley.com/doi/abs/10.1046/j.1365-3040.1998.00323.x – (On our blog : https://plantstomata.wordpress.com/2019/03/05/co2%e2%80%90dependent-changes-in-the-zeaxanthin-content-of-stomata-could-modulate-co2%e2%80%90dependent-changes-of-stomatal-apertures-in-the-light/ )

Zhu J., Yu Q., Xu C., Li J., Qin G. (2018) – Rapid Estimation of Stomatal Density and Stomatal Area of Plant Leaves Based on Object-Oriented Classification and Its Ecological Trade-Off Strategy Analysis – forests-09-00616.pdf – (On our blog : https://plantstomata.wordpress.com/2019/08/01/rapid-estimation-of-stomatal-density-and-stomatal-area/ )

Zhu K., Sun Z., Zhao F., Yang T., Tian Z., Lai J., Long B., Li S. (2020) – Remotely sensed canopy resistance model for analyzing the stomatal behavior of environmentally-stressed winter wheat –  ISPRS J. Photogramm. Remote Sens. 168: 197–207 – https://doi.org/10.1016/j.isprsjprs.2020.08.012https://www.sciencedirect.com/science/article/abs/pii/S0924271620302276?via%3Dihub – (On our blog : https://plantstomata.wordpress.com/2022/04/20/remotely-sensed-canopy-resistance-model-for-analyzing-the-stomatal-behavior/ )

Zhu K., Wang A., Wu J., Yuan F., Guan D., Jin C., Zhang Y., Gong C., (2020) – Effects of nitrogen additions on mesophyll and stomatal conductance in Manchurian ash and Mongolian oak – Sci Rep. 10(1): 10038 – doi: 10.1038/s41598-020-66886-x – PMID: 32572068 – PMCID: PMC7308411 – https://pubmed.ncbi.nlm.nih.gov/32572068/ – (On our blog : https://plantstomata.wordpress.com/2021/01/25/improvements-in-leaf-n-content-and-aqp-and-ca-activities-significantly-promote-gm-and-gsc-increases/ )

Zhu M., Assmann S. M. (2017) – Metabolic Signatures in Response to Abscisic Acid (ABA) Treatment in Brassica napus Guard Cells Revealed by Metabolomics – Scientific Reports 7(1) – DOI: 10.1038/s41598-017-13166-w – https://www.researchgate.net/publication/320288731_Metabolic_Signatures_in_Response_to_Abscisic_Acid_ABA_Treatment_in_Brassica_napus_Guard_Cells_Revealed_by_Metabolomics – (On our blog : https://plantstomata.wordpress.com/2018/07/28/metabolic-signatures-in-response-to-aba-in-stomatal-protoplasts/ )

Zhu M., Dai S., Chen S. (2012) – The stomata frontline of plant
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Zhu M., Dai S., Zhu N., Booy A., Simons B., Yi S., Chen S. (2012) – Methyl jasmonate responsive proteins in Brassica napus guard cells revealed by iTRAQ-based quantitative proteomics – J. Proteome Res. 11: 3728–3742 – DOI: 10.1021/pr300213k – https://pubs.acs.org/doi/abs/10.1021/pr300213k – (On our blog : https://plantstomata.wordpress.com/2018/07/28/meja-responsive-molecular-mechanisms-in-stomata/

Zhu M., Geng S., Chakravorty D., Guan Q., Chen S, Assmann S. M. (2020) – Metabolomics of red-light-induced stomatal opening in Arabidopsis thaliana: Coupling with abscisic acid and jasmonic acid metabolism – Plant J. 101(6): 1331-1348 – doi: 10.1111/tpj.14594 – Epub 2019 Dec 15 – PMID: 31677315 – https://pubmed.ncbi.nlm.nih.gov/31677315/ – (On our blog : https://plantstomata.wordpress.com/2021/06/29/stomatal-opening-response-to-red-light-is-correlated-with-a-decrease-in-guard-cell-abscisic-acid-content-and-an-increase-in-jasmonic-acid-content/ )

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Zhu M., Li X., Su Y.-H., Lu L., Huang C.-L., Ninemets Ü. (2011) – Seasonal fluctuations and temperature dependence in photosynthetic parameters and stomatal conductance at the leaf scale of Populus euphratica Oliv. – Tree Physiology  31(2): 178–195 – https://doi.org/10.1093/treephys/tpr005 – https://academic.oup.com/treephys/article/31/2/178/1716620 – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/72284 )

Zhu M., Simons B., Zhu N., Oppenheimer D. G., Chen S. (2010) – Analysis of abscisic acid responsive proteins in Brassica napus guard cells by multiplexed isobaric tagging – J. Proteomics 73: 790–805 – doi: 10.1016/j.jprot.2009.11.002 – https://www.sciencedirect.com/science/article/pii/S1874391909003303 – (On our blog : https://plantstomata.wordpress.com/2018/07/28/inventory-of-aba-responsive-proteins-and-new-proteins-for-further-investigation-of-their-functions-in-guard-cell-aba-signaling/ )

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Zhu P., Zhuang Q, Ciais P., Welp L., Li W., Xin Q. (2017) – Elevated atmospheric CO2 negatively impacts photosynthesis through radiative forcing and physiology-mediated climate feedback – Geophys. Res. Lett. 44 – doi:10.1002/2016GL071733https://www.eaps.purdue.edu/ebdl/pdfs/Zhu_GRL_2017.pdf – (On our blog : https://plantstomata.wordpress.com/2022/02/07/stomatal-closure-reduces-evapotranspiration-and-increases-sensible-heat-emissions-from-ecosystems-leading-to-decreased-atmospheric-moisture-and-precipitation-and-local-warming/ )

Zhu X., Cao Q., Sun L., Yang X., Yang W., Zhang H. (2018) – Stomatal Conductance and Morphology of Arbuscular Mycorrhizal Wheat Plants Response to Elevated CO2 and NaCl Stress – Front Plant Sci. 9: 1363 – doi: 10.3389/fpls.2018.01363 – eCollection 2018 – https://www.ncbi.nlm.nih.gov/pubmed/30283478 – (On our blog : https://plantstomata.wordpress.com/2019/09/09/am-symbiosis-alters-stomatal-morphology-by-changing-sd-and-the-size-of-the-stomatal-guard-cells-and-pores/ )

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Zhu Y., Huang L., Dang C. H., Wang H. X., Jiang G. B., Li Y. Z., Zhang Z. C., Lou X., Zheng Y. P. (2016) – Effects of high temperature on leaf stomatal traits and gas exchange parameters of blueberry – Trans CSAE 32(1): 218–225 (in Chinese with English abstract) –

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