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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., Li N., Li H., Zhang S., Zhang X., Yan X., Wang Z., Yang Y., Zhang S. (2023) – Overexpression of NtGCN2 improves drought tolerance in tobacco by regulating proline accumulation, ROS scavenging ability, and stomatal closure – Plant Physiol Biochem.198: 107665 – doi: 10.1016/j.plaphy.2023.107665 – Epub 2023 Mar 28 – PMID: 37018865 – https://pubmed.ncbi.nlm.nih.gov/37018865/ – (On our blog : https://plantstomata.wordpress.com/2023/05/27/ntgcn2-might-regulate-drought-tolerance-by-regulating-proline-accumulation-reactive-oxygen-species-ros-scavenging-and-stomatal-closure-in-tobacco-and-may-have-the-potential-for-application-in-the/ )
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., Wang Y., Sang T., Lin Z., Li R., Ren W., Shen X., Zhao B., Wang X., Zhang X., Zhou S., Dai S., Hu H., Song C.-P., Wang P. (2023) – Cell type-specific proteomics uncovers a RAF15-SnRK2.6/OST1 kinase cascade in guard cells – Journal of Integrative Plant Biology – https://doi.org/10.1111/jipb.13536 – https://onlinelibrary.wiley.com/doi/10.1111/jipb.13536 – (On our blog : https://plantstomata.wordpress.com/2023/06/13/how-aba-activates-snrk2-6-ost1-in-guard-cells-and-represents-a-resource-potentially-providing-further-insights-into-the-molecular-basis-of-stomatal-guard-cell-and-mesophyll-cell-development-metabolis/ )
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/B978-0-12-811562-6.00009-8 – https://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.18.00736 – http://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) – https://scholars.uab.edu/display/pub2430955 – (On our blog : https://plantstomata.wordpress.com/2023/01/01/the-change-of-stomata-sensitivity-of-aba-by-light-dark-could-be-regulated-through-the-change-of-dissociation-contant-to-the-aba-binding-proteins/ )
Wang J. (2024) – Unlocking-the-potential-of-AI-for-studying-leaf-stomata : A-valuable-image-dataset-for-ecologists-and-plant-scientists – Plant Science and Anatomy & Physiology 2024 – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/123224)
Wang J., Cui D., Wang L., Du M., Yin Y., Ma R., Sun H., Jiao Z. (2021) – Atmospheric pressure plasma treatment induces abscisic acid production, reduces stomatal aperture and improves seedling growth in Arabidopsis thaliana, Plant Biology 23(4): 564-573 – https://doi.org/10.1111/plb.13245 – https://onlinelibrary.wiley.com/doi/10.1111/plb.13245 – (On our blog : https://plantstomata.wordpress.com/2023/05/27/capps-treatment-accelerates-aba-accumulation-in-arabidopsis-at-early-growth-stages-and-aba-regulates-ros-and-ca2-concentrations-to-affect-stomatal-aperture/ )
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.932 – https://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-2022-50 – https://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.2021.146968 – https://en.x-mol.com/paper/article/1382786176436428800 – https://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.180928 – http://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., Bai X., Qiao Y., Si L., Yu Z., Ni C., Li T., Guo C., Qiao K. (2022) – tae-miR9674a, a microRNA member of wheat, confers plant drought and salt tolerance through modulating the stomata movement and ROS homeostasis – Plant Biotechnology Reports 17(9): – DOI: 10.1007/s11816-022-00787-5 – ww.researchgate.net/publication/363035183 – (On our blog : https://plantstomata.wordpress.com/2024/02/03/tae-mir9674a-is-an-essential-mediator-in-plant-osmotic-stress-tolerance-by-positively-regulating-osmotic-stress-acclimation-cellular-ros-homeostasis-and-related-defensive-processes-modulating-the-s/)
Wang L., Chang C. (2023) – The exploration of stomatal development for crop stress resistance – Journal of Experimental Botany – DOI: 10.1093/jxb/erad477 – https://www.researchgate.net/publication/375913630 – (On our blog : https://plantstomata.wordpress.com/2024/02/15/the-most-recent-advances-in-studies-of-crop-stomata-formation-and-its-multifaceted-functions-in-abiotic-stress-tolerance/ )
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.2022.05.004 – https://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/ijms22063157 – https://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., Yang K., Le J. (2014) – Organ-specific effects of brassinosteroids on stomatal production coordinate with the action of TOO MANY MOUTHS – Journal of integrative plant biology 57(3): 247-255 – https://doi.org/10.1111/jipb.12285 – https://onlinelibrary.wiley.com/doi/10.1111/jipb.12285 – (On our blog : https://plantstomata.wordpress.com/2023/05/22/the-br-organ-specific-effects-on-stomatal-production-might-coordinate-with-the-tmm-organ-specific-actions/ )
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/plz034 – https://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 P., Qi S., Wang X., Dou L., Jia M.-A., Mao T., Guo Y., Wang X. (2023) – The OPEN STOMATA1-SPIRAL1 module regulates microtubule stability during abscisic acid-induced stomatal closure in Arabidopsis – Plant Cell. 35(1): 260-278 – doi: 10.1093/plcell/koac307 – PMID: 36255272 – PMCID: PMC9806620 – https://pubmed.ncbi.nlm.nih.gov/36255272/ – (On our blog : https://plantstomata.wordpress.com/2023/01/10/spr1-positively-regulates-microtubule-disassembly-during-aba-induced-stomatal-closure-which-depends-on-ost1-mediated-phosphorylation/ )
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 P., Wang S., Chen B., Amir M., Wang L., Chen J., Ma L., Wang X., Liu Y., Zhu K. (2022) – Light and Water Conditions Co-Regulated Stomata and Leaf Relative Uptake Rate (LRU) during Photosynthesis and COS Assimilation: A Meta-Analysis – Sustainability 10.3390/su14052840 – 14(5) : – https://doi.org/10.3390/su14052840 – https://www.mdpi.com/2071-1050/14/5/2840 – (On our blog : https://plantstomata.wordpress.com/2022/12/05/during-plant-photosynthesis-and-cos-assimilation-light-and-water-conditions-co-regulated-the-stomata-and-lru/ )
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 R. (2021) – The application of the replicated spatial point pattern analysis method to the spatial characteristics of stomata of the eight Magnoliaceae species. MD Thesis, Nanjing Forestry University, China –
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.0115395 – https://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.i3.1636 – https://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., Li S., Wang J., Li Q., Xin X. F., Zhou S., Wang Y., Li D., Xu J., Luo Z. Q., He S. Y., Sun W. (2021) – A bacterial kinase phosphorylates OSK1 to suppress stomatal immunity in rice – Nat Commun.12(1): 5479 – doi: 10.1038/s41467-021 -25748-4 – PMID: 34531388 – PMCID: PMC8445998 – https://pubmed.ncbi.nlm.nih.gov/34531388/ – (On our blog : https://plantstomata.wordpress.com/2023/05/22/a-bacterial-kinase-phosphorylates-osk1-to-suppress-stomatal-immunity/ )
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/s11427-016-5106-6 – https://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/10.1175/2008JHM1050.1 – https://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 12: 3403 – https://doi.org/10.1038/s41467-021-23728-2 – https://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 T., Wei Q., Wang Z., Liu W., Zhao X., Ma C., Gao J., Xu Y., Hong B. (2021) – CmNF-YB8 affects drought resistance in chrysanthemum by altering stomatal status and leaf cuticle thickness – Journal of Integrative Plant BiologyVolume 64(3): 741-755 – https://doi.org/10.1111/jipb.13201 – https://onlinelibrary.wiley.com/doi/10.1111/jipb.13201 – (On our blog : https://plantstomata.wordpress.com/2023/05/24/cmnf-yb8-thus-regulates-cmcipk6-and-cmshn3-expression-to-alter-stomatal-movement-and-cuticle-thickness-in-the-leaf-epidermis-thereby-affecting-drought-resistance/ )
Wang T., Yang R., Shi N., Yang J., Yan H., Wang J., Ding Z., Huang W., Luo Q., Lin Y., Gao J., Han M. (2019) – Cu,N-Codoped Carbon Nanodisks with Biomimic Stomata-Like Interconnected Hierarchical Porous Topology as Efficient Electrocatalyst for Oxygen Reduction Reaction – Small 15(43): 1902410 – https://doi.org/10.1002/smll.201902410 – https://onlinelibrary.wiley.com/doi/10.1002/smll.201902410 – (On our blog : https://plantstomata.wordpress.com/2023/12/20/high-quality-2d-cu-n-c-nanodisks-nds-with-biomimic-stomata-like-interconnected-hierarchical-porous-topology-are-synthesized-via-carbonization-of-cu-tetrapyridylporphyrin-tpyp-metal-organic/ )
Wang T., Ye W., Wang Y., Zhang M., Aihara Y., Kinoshita T. (2021) – Protease Inhibitor-Dependent Inhibition of Light-Induced Stomatal Opening – Front. Plant Sci. 12: 735328 – https://doi.org/10.3389/fpls.2021.735328 – https://www.frontiersin.org/articles/10.3389/fpls.2021.735328/full – (On our blog : https://plantstomata.wordpress.com/2023/04/11/pis-suppress-bl-induced-stomatal-opening-at-least-in-part-by-inhibiting-pm-h-atpase-activity-but-not-the-aba-signaling-pathway/ )
Wang T., Zheng L., Xiong D., Wang F., Man J., Deng N., Cui K., Huang J., Peng S., Ling X. (2022) – Stomatal Ratio Showing No Response to Light Intensity in Oryza – Plants (Basel) 12(1): 66 – doi: 10.3390/plants12010066 – PMID: 36616195 – PMCID: PMC9823486 – https://pubmed.ncbi.nlm.nih.gov/36616195/ – (On our blog : https://plantstomata.wordpress.com/2023/03/01/stomatal-traits-of-oryza-tend-to-shift-together-during-plasticity-to-diverse-growing-conditions-but-the-previously-projected-sensitive-trait-stomatal-ratio-does-not-shape-growth-condition/ )
Wang W., Chen Q., Xu S., Liu W.-C., Zhu X., Song C.-P. (2020) – Trehalose-6-phosphate phosphatase E modulates ABA-controlled root growth and stomatal movement in Arabidopsis – Journal of Integrative Plant Biology 62(10): 1518-1534 – https://doi.org/10.1111/jipb.12925 – https://onlinelibrary.wiley.com/doi/10.1111/jipb.12925 – (On our blog : https://plantstomata.wordpress.com/2023/05/24/tppe-is-involved-in-aba-controlled-root-elongation-and-stomatal-movement-by-inducing-ros-accumulation/ )
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-20-11287-2020 – https://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., Shi X., Chen D., Wang F., Zhang H. (2020) – The Brassica napus MYC2 regulates drought tolerance by monitoring stomatal closure – Eur.J.Hortic.Sci. 85 (4) 226-231 | DOI: 10.17660/eJHS.2020/85.4.3– ISSN 1611-4426 print and 1611-4434 online | © ISHS 2020 | European Journal of Horticultural Science | Original article – https://www.pubhort.org/ejhs/85/4/3/index.htm – (On our blog : https://plantstomata.wordpress.com/2024/04/01/123287/ )
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/ert362 –http://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 – PMID: 26945669 – https://pubmed.ncbi.nlm.nih.gov/26945669/ – (On our blog : https://plantstomata.wordpress.com/2023/01/03/a-mechanism-for-chloroplast-mediated-stomatal-closure-involving-the-generation-of-mesophyll-chloroplastic-h2o2-based-on-the-reduced-state-of-the-pq-pool-which-is-calcium-sensing-receptor-cas-and-lh/ )
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. H., Zheng H. L. (2012) – Mechanisms for calcium sensing receptor-regulated stomatal closure in response to the extracellular calcium signal – Plant Signal Behav. 7(2):289-91 – doi: 10.4161/psb.18882 – Epub 2012 Feb 1 – https://pubmed.ncbi.nlm.nih.gov/22415046/ – (On our blog : https://plantstomata.wordpress.com/2023/01/03/nitric-oxide-no-and-the-hydrogen-peroxide-h%e2%82%82o%e2%82%82-accumulated-in-the-stomatal-guard-cell-chloroplast-are-the-two-elements-that-act-downstream-of-the-cas-signaling-and-trigger-the-stom/ )
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/s11051-013-1417-8 – https://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.133.6.768 – https://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/B978-0-12-801922-1.00007-5 – https://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/ery188 – https://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.-L., Gao X.-Q., Wang X.-C. (2011) – Stochastic dynamics of actin filaments in guard cells regulating chloroplast localization during stomatal movement – Plant, Cell & Environment 34(8): 1248-1257 – https://doi.org/10.1111/j.1365-3040.2011.02325.x – https://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.2011.02325.x – (On our blog : https://plantstomata.wordpress.com/2023/06/26/the-stochastic-dynamics-of-actin-filaments-in-guard-cells-regulate-chloroplast-localization-during-stomatal-movement/ )
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.118.4.1421 – http://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.,
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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.2020.00333 – https://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.x – https://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., Chen Z. H., Zhang B., Hills A. (2019) – The role of ion channels in regulating stomatal movement – Plant Cell Reports 38(2): 149-162 –
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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.113.233403 – http://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/erh135 – https://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., Li J., Li C., Liang Y. (2016) – A comparative study of cadmium and zinc uptake and distribution in two contrasting ecotypes of Sedum alfredii – Journal of Hazardous Materials 304: 146-155 –
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/s11738-014-1596-7 – https://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/agronomy10121921 – www.mdpi.com/journal/agronomy – file:///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/ )
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Wang Y., Noguchi K., Terashima I. (2008) – Distinct light responses of the adaxial and abaxial stomata in intact leaves of Helianthus annuus L. – Plant Cell Environ. 31: 1307-1316 – DOI: 10.1111/j.1365-3040.2008.01843.x – https://pubmed.ncbi.nlm.nih.gov/18537998/ – (On our blog : https://plantstomata.wordpress.com/2021/01/05/distinct-light-responses-of-the-adaxial-and-abaxial-stomata/ )
Wang Y., Noguchi K., Terashima I. (2011) – Photosynthesis-dependent and-independent responses of stomata to blue, red and green monochromatic light: differences between the normally oriented and inverted leaves of sunflower –
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Wang Y., Papanatsiou M., Eisenach C., Karnik R., Williams M., Hills A., Lew V. L., Blatt M. R. (2012) – Systems Dynamic Modeling of a Guard Cell Cl− Channel Mutant Uncovers an Emergent Homeostatic Network Regulating Stomatal Transpiration – Plant Physiol 160:1956–1967 – DOI: https://doi.org/10.1104/pp.112.207704 – http://www.plantphysiol.org/content/160/4/1956?ijkey=cfc390beba20130ff1b1ff8b2c4ebc6af21a8836&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2018/02/02/emergent-homeostatic-network-regulating-stomatal-transpiration/ )
Wang Y., Sperry J. S., Anderegg W. R. L., Venturas M. D., Trugman A. T. (2020) – A theoretical and empirical assessment of stomatal optimization modeling – New Phytologist 227: 311-325 – https://doi.org/10.1111/nph.16572 – https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.16572 – (On our blog : https://plantstomata.wordpress.com/2022/04/19/10-different-optimization-models-in-how-they-quantify-the-penalty-and-how-well-they-predict-stomatal-responses-to-the-environment/ )
Wang Y., Sperry J. S., Venturas M. D., Trugman A. T., Love D. M., Anderegg W. R. L. (2019) – The stomatal response to rising CO2 concentration and drought is predicted by a hydraulic trait-based optimization model – Tree Physiology 00: 1-12 – https://doi.org/10.1093/treephys/tpz038 – http://sperry.biology.utah.edu/publications/Wang_et_al_2019_TPH.pdf – (On our blog : https://plantstomata.wordpress.com/2019/06/14/the-stomatal-response-to-rising-co2-concentration-and-drought/ )
Wang Y., Wang Y., Tang Y., Xin-Guang Zhu X.-G. (2022) – Stomata conductance as a goalkeeper for increased photosynthetic efficiency –
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Wang Z.-Q., Liu Q., Wu J.-H., Li J., He J.-M., Zhang Y., Li S. (2020) – Downregulating VAC14 in Guard Cells Causes Drought Hypersensitivity by Inhibiting Stomatal Closure – Front. Plant Sci., 17 December 2020 – https://doi.org/10.3389/fpls.2020.602701 – https://www.frontiersin.org/articles/10.3389/fpls.2020.602701/full – (On our blog : https://plantstomata.wordpress.com/2021/12/04/96685/ )
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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.x – https://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)90207-5 – https://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-zy62 – https://cedar.wwu.edu/wwuet/308/ – (On our blog : https://plantstomata.wordpress.com/2021/12/12/97381/ )
Williams C. N. (1971) – Growth and Productivity of Tapioca (Manihot utilissima) II. Stomatal Functioning and Yield – Experimental Agriculture 7(1): 49-62 – doi:10.1017/S0014479700004786 – https://www.cambridge.org/core/journals/experimental-agriculture/article/abs/growth-and-productivity-of-tapioca-manihot-utilissima-ii-stomatal-functioning-and-yield/7C0B50553A9C3F785886B8B33B1F6609 – (On our blog : https://plantstomata.wordpress.com/2023/06/16/stomatal-functioning-could-be-related-to-canopy-type-and-to-planting-conditions/ )
Williams L. E., Baeza P., Vaughn P. (2012) – Midday measurements of leaf water potential and stomatal conductance are highly correlated with daily water use of Thompson Seedless grapevines – Irrig Sci 30: 201–212 – https://doi.org/10.1007/s00271-011-0276-2 – https://link.springer.com/article/10.1007/s00271-011-0276-2 – (On our blog : https://plantstomata.wordpress.com/2023/03/31/midday-measurements-of-stomatal-conductance-and-%cf%88l-were-significantly-correlated-with-one-another/ )
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 – https://doi.org/10.1111/j.1365-3040.1996.tb00456.x – https://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.1996.tb00456.x – (On our blog : https://plantstomata.wordpress.com/2023/01/04/the-regulation-of-stomatal-conductance-by-light-nitrogen-and-soil-plant-hydraulic-properties/ )
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/10.1038/160364b0 – https://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.a083220 – https://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/1.1.114 – https://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/3.1.110 – https://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/10.1038/166034b0 – https://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 – DOI: 10.1111/j.1399-3054.1950.tb07675.x – Wiley Online Library | –https://eurekamag.com/research/025/526/025526760.php – (On our blog : https://plantstomata.wordpress.com/2017/06/08/stomatal-behaviour-in-buffer-solutions/ )
Willis A. J., Balasubramaniam S. (1968) – STOMATAL BEHAVIOUR IN RELATION TO RATES OF PHOTOSYNTHESIS AND TRANSPIRATION IN PELARGONIUM – New Phytologist 67(2): 265-285 – https://doi.org/10.1111/j.1469-8137.1968.tb06383.x – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/j.1469-8137.1968.tb06383.x – (On our blog : https://plantstomata.wordpress.com/2023/07/22/watering-leads-to-stomatal-closure-at-first-with-decreased-rates-of-photosynthesis-and-transpiration-but-subsequently-leaf-resistance-diminishes-and-the-rates-increase-as-normal-turgor-relations-in/ )
Willmer C. M. (1980) – SOME CHARACTERISTICS OF PHOSPHOENOLPYRUVATE CARBOXYLASE ACTIVITY FROM LEAF EPIDERMAL TISSUE IN RELATION TO STOMATAL FUNCTIONING – New Phytologist 84(4): 593-602 – https://doi.org/10.1111/j.1469-8137.1980.tb04773.x – https://nph.onlinelibrary.wiley.com/doi/10.1111/j.1469-8137.1980.tb04773.x – (On our blog : https://plantstomata.wordpress.com/2023/07/22/aba-does-not-control-stomatal-movements-via-its-effect-on-pep-carboxylase/ )
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.x – https://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 communis – Protoplasma 95(4): 321–332 – https://doi.org/10.1007/BF01291408 – https://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/BF00390794 – https://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 – https://link.springer.com/chapter/10.1007/978-94-011-0579-8_5#citeas – (On our blog : https://plantstomata.wordpress.com/2023/01/04/the-theory-of-gas-diffusion-through-stomata/ )
Willmer C. M., Fricker M. (1996) – The influence of hormones and other naturally occurring compounds on stomatal behaviour – In: Stomata. Springer, Dordrecht – https://doi.org/10.1007/978-94-011-0579-8_7 – https://link.springer.com/chapter/10.1007/978-94-011-0579-8_7 – (On our blog : https://plantstomata.wordpress.com/2023/06/25/groups-of-hormones-such-as-the-cytokinins-may-be-involved-in-the-control-of-stomata/ )
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 – PMID: 4708202 – https://doi.org/10.1016/0024-3205(73)90207-5 – https://pubmed.ncbi.nlm.nih.gov/4708202/ – https://www.sciencedirect.com/science/article/abs/pii/0024320573902075 – (On our blog : https://plantstomata.wordpress.com/2023/01/05/phosphoenolpyruvate-carboxylase-in-leaf-epidermal-tissue-and-its-significance-in-stomatal-movements-2/ )
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 – https://doi.org/10.1111/j.1469-8137.1969.tb06449.x –https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/j.1469-8137.1969.tb06449.x – (On our blog : https://plantstomata.wordpress.com/2016/03/18/the-use-of-detached-epidermis-in-studies-of-stomatal-physiology/ )
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.x – https://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 – https://doi.org/10.1111/j.1469-8137.1970.tb02477.x – https://nph.onlinelibrary.wiley.com/doi/abs/10.1111/j.1469-8137.1970.tb02477.x – (On our blog : https://plantstomata.wordpress.com/2023/01/05/effects-of-some-metabolic-inhibitors-and-temperature-on-ion-stimulated-stomatal-opening/ )
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/10.1038/252126a0 – https://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 Stomatal Movements – Nature 269: 327-328 – https://doi.org/10.1038/269327a0 – https://www.nature.com/articles/269327a0#citeas – (On our blog : https://plantstomata.wordpress.com/2023/01/05/stomatal-guard-cell-malic-acid-metabolism-during-stomatal-movements/ )
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/PP9780767 – http://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/39.4.401 – https://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 – doi: 10.1104/pp.23.1.5 – https://pubmed.ncbi.nlm.nih.gov/16654148/ – (On our blog : https://plantstomata.wordpress.com/2023/01/05/environmental-factors-and-the-movements-of-guard-cells/ )
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: 10.1080/00288233.1971.10421670 – https://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., Davies W. J. (1979) – Farnesol-like antitranspirant activity and stomatal behaviour in maize and Sorghum lines of differing drought tolerance – Plant, Cell & Environment 2(1): 49-57 – https://doi.org/10.1111/j.1365-3040.1979.tb00773.x – https://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.1979.tb00773.x – (On our blog : https://plantstomata.wordpress.com/2024/05/12/there-was-no-consistent-relationship-between-plant-water-stress-and-antitranspirant-level-or-between-stomatal-behaviour-and-antitranspirant-level/ )
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/ )
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Xing Q., Liao J., Cao S., Li M., Lv T., Qi H. (2020) – CmLOX10 positively regulates drought tolerance through jasmonic acid -mediated stomatal closure in oriental melon (Cucumis melo var. makuwa Makino) – Sci Rep. 10(1): 17452 – doi: 10.1038/s41598-020-74550-7 – PMID: 33060707 – PMCID: PMC7562952 – https://pubmed.ncbi.nlm.nih.gov/33060707/ – (On our blog : https://plantstomata.wordpress.com/2023/06/30/important-roles-of-cmlox10-in-the-regulation-of-drought-tolerance-in-oriental-melon-seedlings-through-ja-mediated-stomatal-closure-and-ja-signaling-mediated-feedback-through-cmmyc2/ )
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.13111 –http://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/ )
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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 ([ 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.]) – Chinese Journal of Plant Ecology 38: 868-877 – DOI: 10.3724/SP.J.1258.2014.00081 – https://www.plant-ecology.com/EN/10.3724/SP.J.1258.2014.00081 – (On our blog : https://plantstomata.wordpress.com/2023/01/06/both-habitat-and-plant-type-affect-the-stomatal-response-to-light/ )
Xiong Z., Dun Z., Wang Y., Yang D., Xiong D., Cui K., Peng S., Huang J. (2022) – Effect of Stomatal Morphology on Leaf Photosynthetic Induction Under Fluctuating Light in Rice – Front Plant Sci. 12: 754790 – doi: 10.3389/fpls.2021.754790 – PMID: 35185944 – PMCID: PMC8851391 – https://pubmed.ncbi.nlm.nih.gov/35185944/ – (On our blog : https://plantstomata.wordpress.com/2023/02/05/the-important-role-of-stomatal-morphology-in-regulating-photosynthetic-efficiency-and-plant-growth-under-fluctuating-light-conditions/ )
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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.2021.104757 – https://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. Q., Wang J. J., Peng Y., Huang H., Sun L. L., Yang R., Suo L. N., Wang S. H., Zhao W. C. (2022) – SlMYC2 mediates stomatal movement in response to drought stress by repressing SlCHS1 expression – Front Plant Sci. 13: 952758 – doi: 10.3389/fpls.2022.952758 – PMID: 35937339 – PMCID: PMC9354244 – https://pubmed.ncbi.nlm.nih.gov/35937339/ – (On our blog : https://plantstomata.wordpress.com/2023/03/06/slmyc2-drives-stomatal-closure-by-modulating-the-accumulation-of-flavonol-and-the-ja-and-aba-contents-helping-to-decipher-the-mechanism-of-stomatal-movement-under-drought-stress/ )
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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.2018.12.018 – https://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.2019.02.004 – https://www.ncbi.nlm.nih.gov/pubmed/30798115 – (On our blog : https://plantstomata.wordpress.com/2019/04/04/stomatal-transpiration-of-leaves/ )
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Xu L., Zhao H., Wang J., Wang X., Jia X., Wang L., Xu Z., Li R., Jiang K., Chen Z., Luo J., Xie X., Yi K. (2023) – AIM1-dependent high basal salicylic acid accumulation modulates stomatal aperture in rice – New Phytologist 238(4): 1420-1430 – https://doi.org/10.1111/nph.18842 – https://nph.onlinelibrary.wiley.com/doi/10.1111/nph.18842 – (On our blog : https://plantstomata.wordpress.com/2023/08/07/the-synthesis-of-basal-sa-in-rice-shoot-is-dependent-on-osaim1-and-the-critical-role-of-the-pal-pathway-in-the-biosynthesis-of-high-basal-level-sa-which-plays-an-important-role-in-the-regulation/ )
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Xu M., Gruber B. D., Delhaize E., White R. G., James R. A., You J., Yang Z., Ryan P. R. (2014) – The barley anion channel, HvALMT1, has multiple roles in guard cell physiology and grain metabolism – Physiologia Plantarum 153(1) : 183-193 – https://doi.org/10.1111/ppl.12234 – https://onlinelibrary.wiley.com/doi/10.1111/ppl.12234 – (On our blog : https://plantstomata.wordpress.com/2023/06/04/hvalmt1-releases-malate-and-perhaps-other-anions-from-guard-cells-to-promote-stomatal-closure/ )
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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/ )
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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/AJB – DOI: 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/ )
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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.2017.04.008 – https://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)2 on quinoa treated with salinity – Peer J. Preprints 4:e1956v1 – https://doi.org/10.7287/peerj.preprints.1956v1 – https://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.63335 – https://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 H., Shah S. S., Zhao W., Liu F. (2020) – Variations in water relations, stomatal characteristics, and plant growth between quinoa and pea under salt-stress conditions – Pak J Bot 52(1): 1-7 –
Yan J., Tsuichihara N., Etoh T., Iwai S. (2007) – Reactive oxygen species and nitric oxide are involved in ABA inhibition of stomatal opening – Plant, Cell & Environment 30(10) : 1320-1325 – https://doi.org/10.1111/j.1365-3040.2007.01711.x – https://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.2007.01711.x – (On our blog :
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.1008094 – https://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 S., McLamore E. S., Dong S., Gao H., Taguchi M., Wang N., Zhang T., Su X., Shen Y. (2015) – The role of plasma membrane H+-ATPase in jasmonate-induced ion fluxes and stomatal closure in Arabidopsis thaliana – The Plant Journal 83(4): 638-649 – https://doi.org/10.1111/tpj.12915 – https://onlinelibrary.wiley.com/doi/10.1111/tpj.12915 – (On our blog : https://plantstomata.wordpress.com/2023/07/08/the-elevation-of-cytosolic-ca2-concentration-and-the-depolarized-pm-drive-the-efflux-of-k-from-the-cell-resulting-in-loss-of-turgor-and-closure-of-the-stomata/ )
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/HORTSCI14482-19 – https://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., 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 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., Zhang J.-H. (2006) – Water Channels Are Involved in Stomatal Oscillations Encoded by Parameter-Specific Cytosolic Calcium Oscillations – Journal of Integrative Plant Biology 48(7): 790-799 – https://doi.org/10.1111/j.1744-7909.2006.00261.x – https://onlinelibrary.wiley.com/doi/10.1111/j.1744-7909.2006.00261.x – (On our blog : https://plantstomata.wordpress.com/2023/05/25/water-channels-are-involved-in-stomatal-oscillation-as-a-downstream-element-of-ca2cyt-oscillation-signaling/ )
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.2020.601478 – https://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-2018-0241 – https://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.2011.09.006 – https://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 J., Zhang N., Bai J., Duan X., Zhang L., Liu S., Tang X., Jin X., Li S., Si H. (2022) – Stu-miR827-Targeted StWRKY48 Transcription Factor Negatively Regulates Drought Tolerance of Potato by Increasing Leaf Stomatal Density – Int J Mol Sci. 23(23): 14805 – doi: 10.3390/ijms232314805 – PMID: 36499135 – PMCID: PMC9741430 – https://pubmed.ncbi.nlm.nih.gov/36499135/ – (On our blog : https://plantstomata.wordpress.com/2023/02/05/suppression-of-stu-mir827-might-lead-to-overexpression-of-stwrky48-which-may-contribute-to-negatively-regulating-the-drought-adaptation-by-increasing-the-stomatal-density/ )
Yang K., Yang J., Lv C., Hu Z., Yu L., Sun W. (2023) – Effects of three patterns of elevated CO2 in single and multiple generations on photosynthesis and stomatal features in rice – Annals of Botany 131(3): 463–473 – https://doi.org/10.1093/aob/mcad021 – https://academic.oup.com/aob/article-abstract/131/3/463/7008608?redirectedFrom=fulltext&utm_source=etoc&utm_campaign=aob&utm_medium=email – (On our blog : https://plantstomata.wordpress.com/2023/04/08/elevated-co2-retained-intergenerational-effects-on-photosynthesis-and-stomatal-features-and-there-were-no-multigenerational-differences-in-the-effects-of-gradually-elevated-co2-and/ )
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.12154 – https://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 development – https://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.1819345116 – https://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.2020.0257 – https://www.plant-ecology.com/EN/10.17521/cjpe.2020.0257 – (On our blog : https://plantstomata.wordpress.com/2021/11/28/96405/ )
Yang L., Han M., Zhou G., Li J. (2007) – The changes in water-use efficiency and stoma density of Leymus chinensis along Northeast China Transect – Acta Ecologica Sinica 27(1): 16-24 – https://doi.org/10.1016/S1872-2032(07)60006-7 – https://www.sciencedirect.com/science/article/abs/pii/S1872203207600067 – (On our blog : https://plantstomata.wordpress.com/2023/01/06/changes-in-water-use-efficiency-and-stomata-density/ )
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.2021.668797 – https://www.frontiersin.org/articles/10.3389/fpls.2021.668797/full – (On our blog : https://plantstomata.wordpress.com/2021/11/09/95163/ )
Yang M., He J;, Sun Z., Li Q., Cai J., Zhou Q, Wollenweber B., Jiang D., Wang X. (2023) – Drought priming mechanisms in wheat elucidated by in-situ determination of dynamic stomatal behavior -Front Plant Sci.:14: 1138494 – doi: 10.3389/fpls.2023.1138494 – eCollection 2023 – https://pubmed.ncbi.nlm.nih.gov/36875605/ – (On our blog : https://plantstomata.wordpress.com/2024/03/18/priming-promoted-faster-stomatal-closure-under-drought-stress-and-faster-reopening-during-post-drought-recovery-in-relation-to-non-primed-plants-thereby-enhancing-overall-drought-tolerance/ )
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 M. B., Yang J. L., Yang J. Y., Liang N., Qing H. (2007) – Changes on characteristics of the leaf epidermis and genetic diversity of Caragana davazamcii in different habitats in Ordos plateau, China – Journal of Plant Ecology (Chinese Version) 31: 1181–1189 (in Chinese with English abstract) –
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 – https://doi.org/10.1006/jtbi.1997.0583 – https://www.sciencedirect.com/science/article/abs/pii/S002251939790583X – (On our blog : https://plantstomata.wordpress.com/2023/01/06/a-model-to-describe-stomatal-conductance-as-a-function-of-photosynthetically-active-radiation-leaf-water-potential-leaf-temperature-and-vapor-pressure-difference/ )
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.-J., Sun M., Zhang Y.-J., Cochard H., Cao K.-F. (2014) – Strong leaf morphological, anatomical, and physiological responses of a subtropical woody bamboo (Sinarundinaria nitida) to contrasting light environments – Plant Ecology 215(1): 97-109 – http://www.jstor.org/stable/24552072 – (On our blog : https://plantstomata.wordpress.com/2023/04/29/stomatal-size-and-leaf-phosphorous-concentration-per-unit-mass-remained-relatively-constant-regardless-of-light-regime/ )
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/koab260 – https://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., Gavya L., Zhou S., Urano D., –Lau S. (2022) – Abscisic acid regulates stomatal production by imprinting a SnRK2 kinase–mediated phosphocode on the master regulator SPEECHLESS – SCIENCE ADVANCES 8(40): – DOI: 10.1126/sciadv.add2063 – https://www.science.org/doi/10.1126/sciadv.add2063 – (On our blog : https://plantstomata.wordpress.com/2022/10/15/regulation-of-stomatal-production-by-imprinting-a-snrk2-kinase-mediated-phosphocode-on-the-master-regulator-speechless/ )
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-I – https://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.-H., Xi Z., Li J., Feng X., Zhu X., Guo S., Song C. (2021) – Deep Transfer Learning-Based Multi-Object Detection for Plant Stomata Phenotypic Traits Intelligent Recognition – IEEE/ACM Transactions on Computational Biology and Bioinformatics PP(99):1-1 – DOI: 10.1109/TCBB.2021.3137810 – https://dl.acm.org/doi/abs/10.1109/TCBB.2021.3137810 – (On our blog : https://plantstomata.wordpress.com/2024/01/28/for-different-cultivars-multi-scales-rich-background-features-high-density-and-small-stomata-object-images-the-proposed-method-can-precisely-locate-multiple-stomata-in-microscope-images-and-autom/ )
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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.x – https://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/BF02900687 – https://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.16.01050 – http://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 C, Song Z., Jin P., Zhou X., Zhang H. (2021) – Xylooligosaccharides induce stomatal closure via salicylic acid signaling-regulated reactive oxygen species and nitric oxide production in Arabidopsis – Physiologia Plantarum 172(4): 1908-1918 – https://doi.org/10.1111/ppl.13403 – https://onlinelibrary.wiley.com/doi/10.1111/ppl.13403 – (On our blog : https://plantstomata.wordpress.com/2023/07/17/xylooligosaccharides-can-elicit-stomatal-closure-via-salicylic-acid-signaling-mediated-production-of-reactive-oxygen-species-and-nitric-oxide-in-a-manner-independent-of-aba-signaling/ )
Zhang C., Tetteh C., Luo S., Jin P., Hao X., Sun M., Fang N., Liu Y. Zhang H. (2024) – Exogenous application of pectin triggers stomatal closure and immunity in Arabidopsis – Molecular Plant Pathology 25(2): e13438 – https://doi.org/10.1111/mpp.13438 – https://bsppjournals.onlinelibrary.wiley.com/doi/10.1111/mpp.13438 – (On our blog : https://plantstomata.wordpress.com/2024/03/30/exogenous-pectin-induced-stomatal-closure-was-associated-with-ros-and-no-production-regulated-by-aba-and-sa-signalling-contributing-to-defence-against-pst-dc3000-in-arabidopsis/ )
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.1673-5102.2021.03.016 – http://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., Spiegelhalder R. P., Abrash E. B., Nunes T. D.G., Hidalgo I., Anleu Gil M. X., Jesenofsky B., Lindner H., Bergmann D. C., Raissig M. T. (2022) – Opposite polarity programs regulate asymmetric subsidiary cell divisions in grasses – Elife. 2022 Dec 20;11:e79913 – doi: 10.7554/eLife.79913 – PMID: 36537077 – PMCID: PMC9767456 – https://pubmed.ncbi.nlm.nih.gov/36537077/ – (On our blog : https://plantstomata.wordpress.com/2023/01/11/two-opposing-polarity-domains-that-coordinate-the-stomatal-subsidiary-cell-division-a-process-crucial-for-grass-stomatal-physiology/ )
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-R – https://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 ([ 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.]) – Acta Prataculturae Sinica 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., Wang B., Lu F., Zhang X. (2023) – Rotating Stomata Measurement Based on Anchor-Free Object Detection and Stomata Conductance Calculation – Plant Phenomics 5(9) – DOI: 10.34133/plantphenomics.0106 – https://www.researchgate.net/publication/374393447 – (On our blog : https://plantstomata.wordpress.com/2024/01/29/a-novel-approach-named-deeprsd-deep-learning-based-rotating-stomata-detection-for-detecting-rotating-stomata-and-calculating-stomata-basic-traits-at-the-same-time-simultaneously-the-stomata-cond/ )
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/erq189 – https://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., Ni L., Liu Y., Wang Y., Zhang A., Tan M., Jiang M. (2016) – SnRK2. 6-mediated channel phosphorylation controls stomatal aperture and transpiration by modulating ion flux – Plant Cell 28(11): 2894-2907 –
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. (2023) – Estimating crop stomatal conductance through high-throughput plant phenotyping (Master’s Thesis) – Biological Systems Engineering–Dissertations, Theses, and Student Research – Department of Biological Systems Engineering, University of Nebraska, Lincoln – https://digitalcommons.unl.edu/biosysengdiss/141/ – (On our blog : https://plantstomata.wordpress.com/2023/05/10/the-potential-of-estimating-gs-from-remote-sensing-and-field-phenotyping-platforms-to-help-growers-obtain-information-about-the-water-status-of-crops-and-plan-irrigation-more-efficiently/ )
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/37.10.1479 – https://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.2018.10.015 – https://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 Roots – https://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 –
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 K., Xue M., Qin F., He Y., Zhou Y. (2023) – Natural polymorphisms in ZmIRX15A affect water-use efficiency by modulating stomatal density in maize – Plant Biotechnology Journal Early View – Online Version of Record before inclusion in an issue – https://doi.org/10.1111/pbi.14153 – https://onlinelibrary.wiley.com/doi/10.1111/pbi.14153 – (On our blog : https://plantstomata.wordpress.com/2023/08/15/genetic-insights-into-the-natural-variation-of-leaf-sd-in-maize-and-the-identified-loci-or-genes-can-serve-as-direct-targets-for-enhancing-drought-resistance-in-molecular-assisted-maize-breeding/ )
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/f11040402 – https://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., Shi X., Zhang Y., Wang J., Yang J., Ishida T., Jiang W., Han X., Kang J., Wang X., Pan L., Lv S., Cao B., Zhang Y., Wu J., Han H., Hu Z., Cui L., Sawa S., He J., Wang G. (2019) – CLE9 peptide-induced stomatal closure is mediated by abscisic acid, hydrogen peroxide, and nitric oxide in Arabidopsis thaliana – Plant, Cell & Environment 42(3): 1033-1044 – https://doi.org/10.1111/pce.13475 – https://onlinelibrary.wiley.com/doi/10.1111/pce.13475 – (On our blog : https://plantstomata.wordpress.com/2023/06/09/a-novel-aba-dependent-function-of-cle9-in-the-regulation-of-stomatal-apertures/ )
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 M., Gao H., Chen S., Wang X., Mo W., Yang X., Wang X., Wang Z., Wang R. (2022) – Linkages between stomatal density and minor leaf vein density across different altitudes and growth forms – Front Plant Sci. 13: 1064344 – doi: 10.3389/fpls.2022.1064344 – PMID: 36561450 – PMCID: PMC9765094 – https://pubmed.ncbi.nlm.nih.gov/36561450/ – (On our blog : https://plantstomata.wordpress.com/2023/01/08/coordinating-stomatal-number-and-minor-vein-length-within-one-leaf-rather-than-stomatal-and-vein-density-may-be-a-common-choice-of-plants-in-the-fluctuating-environment/ )
Zhang N., Berman S. R., Joubert D., Vialet-Chabrand S., Marcelis L. F. M., Kaiser E. (2022) – Variation of Photosynthetic Induction in Major Horticultural Crops Is Mostly Driven by Differences in Stomatal Traits – Frontiers in Plant Science 13 [860229] – https://doi.org/10.3389/fpls.2022.860229 – https://research.wur.nl/en/publications/variation-of-photosynthetic-induction-in-major-horticultural-crop – (On our blog : https://plantstomata.wordpress.com/2023/01/22/manipulating-stomatal-traits-may-speed-up-photosynthetic-induction-and-growth-of-horticultural-crops-under-natural-irradiance-fluctuations/ )
Zhang N. (2023) – Artificially modulating stomatal development may improve crop stress tolerance – Phys. Org. – https://phys.org/news/2023-06-artificially-modulating-stomatal-crop-stress.html – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/116692 )
Zhang Q., Peng S., Li Y. (2019) – Increase rate of light-induced stomatal conductance is related to stomatal size in the genus Oryza – J Exp Bot. 70(19): 5259-5269 – doi: 10.1093/jxb/erz267 – PMID: 31145797 – PMCID: PMC6793446 – https://pubmed.ncbi.nlm.nih.gov/31145797/ – (On our blog : https://plantstomata.wordpress.com/2023/02/05/the-influence-of-stomatal-size-on-dynamic-photosynthesis-is-correlated-with-%ce%bb-and-gsinitial/ )
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., Gao R. (2000) – Diurnal Changes of Gas Exchange, Chlorophyll Fluorescence, and Stomatal Aperture of Hybrid Poplar Clones Subjected to Midday Light Stress – Photosynthetica 37: 559–571 – DOI: 10.1023/A:1007119524389 – https://ps.ueb.cas.cz/artkey/phs-199914-0011_diurnal-changes-of-gas-exchange-chlorophyll-fluorescence-and-stomatal-aperture-of-hybrid-poplar-clones-subjec.php – (On our blog : https://plantstomata.wordpress.com/2024/01/11/midday-depression-of-photosynthesis-can-be-attributed-to-both-stomatal-and-non-stomatal-limitations/ )
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., Ma K., Chen L. (2002) – Tempo-spatial variations in stomatal conductance, aperture and density of Ligustrum sinense acclimated to different light environments – Acta Botany of Sinica 44: 1225–1232 – https://europepmc.org/article/cba/378247 – (On our blog : https://plantstomata.wordpress.com/2023/04/20/the-sensitivity-of-stomata-to-changing-environment-for-high-light-leaves-was-higher-than-that-for-low-light-leaves-which-may-also-relative-to-the-higher-stomatal-density-for-the-high-light-leaves/ )
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.0040080 – https://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/s003440010021 – https://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 S. Q., Outlaw W. H., Chollet R. ( 1994) – Lessened malate inhibition of guard-cell phosphoenolpyruvate carboxylase velocity during stomatal opening – FEBS Letters 352(1): 45-48 – https://doi.org/10.1016/0014-5793(94)00916-3 – https://febs.onlinelibrary.wiley.com/doi/10.1016/0014-5793%2894%2900916-3 – (On our blog : https://plantstomata.wordpress.com/2023/05/29/the-lessened-sensitivity-of-guard-cell-pepc-activity-to-malate-inhibition-is-an-important-regulatory-feature-of-stomatal-opening/ )
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.2017.06.010 – https://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 T.-Y., Li Z.-Q., Zhao Y.-D., Shen W.-J., Chen M.-S., Gao H.-Q., Ge X.-M., Wang H.-Q., Xue Li X., He J.-M. (2021) – Ethylene-induced stomatal closure is mediated via MKK1/3–MPK3/6 cascade to EIN2 and EIN3 – Journal of Integrative Plant Biology 63(7): 1324-1340 – https://doi.org/10.1111/jipb.13083 – https://onlinelibrary.wiley.com/doi/10.1111/jipb.13083 – (On our blog : https://plantstomata.wordpress.com/2023/05/25/the-mkk1-3-mpk3-6-cascade-mediates-ethylene-induced-stomatal-closure-by-functioning-downstream-of-etr1-ctr1-and-h2o2-to-interact-with-ein2-thereby-promoting-ein3-accumulation-and-ein3/ )
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., Calla B., Thiruppathi D. (2021) – Deep learning-based high-throughput phenotyping accelerates gene discovery for stomatal traits – Plant Physiol. 187(3): 1273-1275 – doi: 10.1093/plphys/kiab398 – PMID: 34734281 – PMCID: PMC8566201 – https://academic.oup.com/plphys/article/187/3/1273/6420538 – (On our blog : https://plantstomata.wordpress.com/2023/08/15/deep-learning-based-high-throughput-phenotyping-accelerates-gene-discovery-for-stomatal-traits/ )
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.106.091405 – http://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 W. (炜 张), Zhao Y. (杨 赵), Guo Y. (岩 郭), Ye K. (克穷 叶) (2012) – Plant Actin-binding Protein SCAB1 Is Dimeric Actin Cross-linker with Atypical Pleckstrin Homology Domain – PROTEIN STRUCTURE AND FOLDING 287(15): 11981-11990 – https://doi.org/10.1074/jbc.M111.338525 – https://www.jbc.org/article/S0021-9258(20)53123-2/fulltext – (On our blog : https://plantstomata.wordpress.com/2023/03/08/scab1-is-a-novel-plant-specific-actin-binding-protein-that-binds-bundles-and-stabilizes-actin-filaments-and-regulates-stomatal-movement/ )
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.8927 – https://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.7290086 – https://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., Zhang Y., Tian J., Ma N., Wang Y.-P. (2022) – CO2 fertilization is spatially distinct from stomatal conductance reduction in controlling ecosystem water-use efficiency increase – Environ. Res. Lett. 17: 054048 – DOI 10.1088/1748-9326/ac6c9c – https://iopscience.iop.org/article/10.1088/1748-9326/ac6c9c – (On our blog : https://plantstomata.wordpress.com/2023/04/11/the-co2-fertilization-effect-on-photosynthesis-23-was-similar-to-the-co2-suppression-effect-on-stomatal-conductance-28/ )
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.2016.08.066 – https://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/v1 – https://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/ )
Zhang Y., Kaiser E., Li T., Marcelis L. F. M., (2022) – NaCl affects photosynthetic and stomatal dynamics by osmotic effects and reduces photosynthetic capacity by ionic effects in tomato – Journal of Experimental Botany 73(11): 3637-3650 – https://doi.org/10.1093/jxb/erac078 – https://academic.oup.com/jxb/article-abstract/73/11/3637/6537450?redirectedFrom=fulltext – (On our blog : https://plantstomata.wordpress.com/2023/04/10/nacl-impacts-dynamic-stomatal-and-photosynthetic-kinetics-by-osmotic-effects-and-reduces-photosynthetic-capacity-by-ionic-effects/ )
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., Liu B., Jia G., Yu G., Zhang X., Yin X., Zhao Z., Cheng C., Wang Y., Xin Y. (2022) – Scaling Up from Leaf to Whole-Plant Level for Water Use Efficiency Estimates Based on Stomatal and Mesophyll Behaviour in Platycladus orientalis – Water 14(2): 263 – DOI: 10.3390/w14020263 – https://www.researchgate.net/publication/357904238_Scaling_Up_from_Leaf_to_Whole-Plant_Level_for_Water_Use_Efficiency_Estimates_Based_on_Stomatal_and_Mesophyll_Behaviour_in_Platycladus_orientalis – (On our blog : https://plantstomata.wordpress.com/2023/07/27/in-shaping-the-expression-of-the-short-term-water-use-efficiencyp-the-role-of-both-stomatal-gsw-and-mesophyll-conductance-gmwere-emphasized/ )
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., Oren R., Kang S. (2012) – Spatiotemporal variation of crown-scale stomatal conductance in an arid Vitis vinifera L. cv. Merlot vineyard: direct effects of hydraulic properties and indirect effects of canopy leaf area – Tree Physiology 32(3): 262–279 – https://doi.org/10.1093/treephys/tpr120 – https://academic.oup.com/treephys/article/32/3/262/1686919 – (On our blog : https://plantstomata.wordpress.com/2023/02/05/spatiotemporal-variation-of-crown-scale-stomatal-conductance/ )
Zhang Y., Su J., Wu T., Wu Y. (2019) – New insights into the regulation of stomatal development and patterning – International Journal of Molecular Sciences 20(15): 3783-
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/ ijms22189892 – file:///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.-D., Véry A.-A., Wang L.-M., Deng Y.-W., Sentenac H., Huang D.-F. (2010) – A K+ channel from salt-tolerant melon inhibited by Na+– New Phytologist 189(3): Special Issue: Featured papers on ‘Unearthing the truffle genome’ : 856-868 – https://doi.org/10.1111/j.1469-8137.2010.03526.x – https://nph.onlinelibrary.wiley.com/doi/10.1111/j.1469-8137.2010.03526.x – (On our blog : https://plantstomata.wordpress.com/2023/07/24/expressed-in-guard-cells-melon-inward-rectifying-k-channel-mirk-might-control-na-arrival-to-the-shoots-via-regulation-of-stomatal-aperture-by-na/ )
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 – Epub 2015 Apr 2 – PMID: 25843888 – PMCID: PMC4406870 – https://pubmed.ncbi.nlm.nih.gov/25843888/ – (On our blog : https://plantstomata.wordpress.com/2023/01/07/breaking-of-asymmetry-in-the-stomatal-lineage-basl-is-polarized-to-control-stomatal-asymmetric-division/ )
Zhang Y., Xu W., Li Z., Deng X. W., Wu W., Xue Y. (2008) – F-box protein DOR functions as a novel inhibitory factor for abscisic acid-induced stomatal closure under drought stress in Arabidopsis – Plant Physiol. 148(4): 2121-2133 – doi: 10.1104/pp.108.126912 – Epub 2008 Oct 3 – PMID: 18835996 – PMCID: PMC2593669 – https://pubmed.ncbi.nlm.nih.gov/18835996/ – (On our blog : https://plantstomata.wordpress.com/2023/06/09/dor-acts-independent-of-phospholipase-dalpha1-in-an-aba-signaling-pathway-to-inhibit-the-aba-induced-stomatal-closure-under-drought-stress/ )
Zhang Y., Xue Y. (2009) – DOR: a link between an F-box protein and guard cell ABA signaling – Plant Signal Behav 4(5): 470-471 – doi: 10.1104/pp.108.126912 – Epub 2009 May 24 – PMID: 19816119 – PMCID: PMC2676770 – https://pubmed.ncbi.nlm.nih.gov/19816119/ – (On our blog : https://plantstomata.wordpress.com/2023/06/09/dor-is-a-guard-cell-preferential-f-box-protein-it-likely-forms-two-negative-feedback-regulatory-loops-for-the-aba-induced-stomatal-closure-under-drought-conditions-in-arabidopsis/ )
Zhang Y., Yang S. J., Sun M., Cao K. F. (2014) – Stomatal traits are evolutionarily associated with vein density in basal angiosperms ([ 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.]) – Plant Science Journal 32: 320-328 – https://www.cabdirect.org/cabdirect/abstract/20143327314 – (On our blog : https://plantstomata.wordpress.com/2023/01/07/stomatal-traits-are-evolutionarily-associated-with-vein-density-in-basal-angiosperms/ )
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. 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.2016.02.018 – https://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 – doi: 10.1080/15592324.2016.1183088 – PMID: 27171851 – PMCID: PMC4973779 – https://pubmed.ncbi.nlm.nih.gov/27171851/ – (On our blog : https://plantstomata.wordpress.com/2023/01/08/mutating-nia1-and-nia2-impaired-nearly-all-the-key-components-of-guard-cell-aba-signaling-pathway-in-arabidopsis/ )
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/10.1101/2020.09.22.309427 – https://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 – PMID: 29570668 – PMCID: PMC5979362 – DOI: 10.3390/ijms19040963 – https://pubmed.ncbi.nlm.nih.gov/29570668/ – (On our blog : https://plantstomata.wordpress.com/2023/01/08/the-roles-of-important-plasma-membrane-and-tonoplast-ion-transporters-that-are-involved-in-regulating-stomatal-movement/ )
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.1812092116 – https://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 J., Zhang W., da Silva J. A. T., Liu X., Duan J. (2021) – Rice histone deacetylase HDA704 positively regulates drought and salt tolerance by controlling stomatal aperture and density – Planta 254(4): 79 –
Zhao J. R. (2023) – The relationship between the wettability and the density of stomata – Theoretical and Natural Science 6(1): 359-363 – DOI: 10.54254/2753-8818/6/20230285 – https://www.researchgate.net/publication/372883982 – (On our blog : https://plantstomata.wordpress.com/2024/01/31/elm-leaves-ulmaceae-lower-surface-with-superhydrophobic-function-is-covered-by-large-amount-of-stomata-while-the-bottom-surface-with-hydrophilic-performance-is-smooth-and-covered-by-a-small-amount/ )
Zhao J. T., Yang K., Wang X., Ma C., Zhang G Q. (2023) – Effect of Phosphorus Application on Physiological Parameters and Antioxidant Capacity in Alfalfa Leaves – Scientia Agricultura Sinica 56(3): 453-465 – doi: 10.3864/j.issn.0578-1752.2023.03.005 – https://www.chinaagrisci.com/EN/10.3864/j.issn.0578-1752.2023.03.005 – (On our blog : https://plantstomata.wordpress.com/2023/02/14/phosphorus-application-and-stomatal-aperture/ )
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 M. (2022) – Evapotranspiration frequently increases during droughts – Nature Climate Change – DOI: 10.1038/s41558-022-01505-3 – www.nature.com/articles/s41558-022-01505-3 – https://phys.org/news/2022-10-key-drought.html – (On our blog : https://plantstomata.wordpress.com/2022/11/13/109828/ ) – See also https://www.newsclick.in/Plant-Processes-Make-Soil-Drier-During-Droughts
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.16.00078 – http://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.2016.04.042 – https://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., Sun Y., Kjelgren R., Liu X. (2015) – Response of Stomatal Density and Bound Gas Exchange in Leaves of Maize to Soil Water Deficit – Acta Physiologiae Plantarum 37(1): 1-9 – doi: 10.1007/s11738-014-1746-y –
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/FP16012 – http://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., 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) – DOI: 10.1093/aobpla/plaa047 – https://www.researchgate.net/publication/344703098_Difference_between_emergent_aquatic_and_terrestrial_monocotyledonous_herbs_in_relation_to_the_coordination_of_leaf_stomata_with_vein_traits – (On our blog : https://plantstomata.wordpress.com/2023/05/18/the-differences-in-water-supply-between-emergent-aquatic-and-terrestrial-plants-modify-the-coordination-of-their-leaf-veins-and-stomatal-traits-2/ )
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 – PMID: 28526823 – PMCID: PMC5438398 – DOI: 10.1038/s41598-017-02448-y – https://pubmed.ncbi.nlm.nih.gov/28526823/ – (On our blog : https://plantstomata.wordpress.com/2023/01/08/the-significance-of-sv-stomatal-number-per-minor-vein-length-and-new-insight-into-the-coordination-between-stomatal-number-and-minor-vein-length/ )-
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.2010.11.024 – http://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.1522840113 – https://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.111.086546 – http://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 Y. Y., Yan F., Hu L. P., Zhou X. T., Zou Z. R., Cui L. R. (2015) – Effects of exogenous 5-aminolevulinic acid on photosynthesis, stomatal conductance, transpiration rate, and PIP gene expression of tomato seedlings subject to salinity stress – Genet. Mol. Res. 14: 6401–6412 – doi: 10.4238/2015.June.11.16 – https://www.funpecrp.com.br/gmr/year2015/vol14-2/pdf/gmr5197.pdf – (On our blog : https://plantstomata.wordpress.com/2022/12/03/effects-of-exogenous-5-aminolevulinic-acid-on-photosynthesis-and-stomatal-conductance/ )
Zhao Z. (2011) – Arabidopsis Stomatal Opening and Closing Experiment – Bio-101: e74 – DOI: 10.21769/BioProtoc.74 – https://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 – DOI: 10.1021/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/ )
Zhen S., Bugbee B. (2020) – Steady-state stomatal responses of C3 and C4 species to blue light fraction: Interactions with CO2 concentration – Plant, Cell & Environment 43(12) : 3020-3032 – https://doi.org/10.1111/pce.13888 – https://onlinelibrary.wiley.com/doi/10.1111/pce.13888 – (On our blog : https://plantstomata.wordpress.com/2024/01/08/the-blue-light-induced-stomatal-opening-minimally-enhanced-photosynthesis-and-consistently-decreased-water-use-efficiency/ )
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.2017.00917 – https://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/10.1080/09064710500321532 – https://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.2011.03.015 – https://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.1901431116 – https://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/ )
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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/ern185 – https://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.13826 – https://www.x-mol.com/paper/1273038415424155648 – (On our blog : https://plantstomata.wordpress.com/2021/01/25/allometric-co-variation-of-xylem-and-stomata)
Zhong Z., He B., Wang Y.-P., Chen H. W., Chen D., Fu Y. H., Chen YU., Guo L., Deng Y., Huang L., Yuan W., Hao X., Tang R., Liu H., Sun L., XIE X., Zhang Y. (2023) – Disentangling the effects of vapor pressure deficit on northern terrestrial vegetation productivity – Science Advances 9(32) – eadf3166 –
DOI: 10.1126/sciadv.adf3166 – https://www.science.org/doi/10.1126/sciadv.adf3166 – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/119485 )
Zhong M., Cerabolini B. E. L., Castro-Díez P., Puyravaud J.-P., Cornelissen J. H. C. (2020) – Allometric co-variation of xylem and stomata across diverse woody seedlings – Plant, Cell & Environment 43(9): 2301-2310 – https://doi.org/10.1111/pce.13826 – https://onlinelibrary.wiley.com/doi/10.1111/pce.13826 – (On our blog :
Zhong Z., He B., Wang Y.-P., Chen H. W., Chen D., Fu Y. H., Chen YU., Guo L., Deng Y., Huang L., Yuan W., Hao X., Tang R., Liu H., Sun L., XIE X., Zhang Y. (2023) – Disentangling the effects of vapor pressure deficit on northern terrestrial vegetation productivity – Science Advances 9 (32) – DOI: 10.1126/sciadv.adf3166 – https://www.science.org/doi/10.1126/sciadv.adf3166 – (On our blog :
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.2019.109547 – https://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.2013.05.009 – http://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 4 – https://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.2018.01965 – https://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 X., Wu W., Yuan M., Wang X. (1999) – Regulation of the inward K+ -channels in stomatal guard cells by cytoskeletal microtubules – Chinese Science Bulletin 44: 919–923 – https://doi.org/10.1007/BF02885065 – https://link.springer.com/article/10.1007/BF02885065#citeas – (On our blog : https://plantstomata.wordpress.com/2023/01/08/the-regulation-of-the-inward-k-channels-in-guard-cells-by-microtubules-may-mediate-the-regulation-of-stomatal-movements-by-cytoskeleton/ )
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 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 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/s11099-005-0071-5 – https://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 Y. M., Han S. J., Liu Y., Jia X. (2005) – Stomatal response ofPinus sylvestriformis to elevated CO2 concentrations during the four years of exposure – Journal of Forestry Research 16: 15–18 – https://link.springer.com/article/10.1007/BF02856846 – (On our blog : https://plantstomata.wordpress.com/2023/04/20/elevated-co2-concentrations-reduced-the-total-stomatal-number-of-whole-needle-by-the-decline-of-stomatal-line-and-changed-the-allocation-pattern-of-stomata-between-upper-and-lower-surface-of-need/ )
Zhou Y. M., Schaub M., Shi L. X., Guo Z. L., Fan A. A., Yan C. F., Wang X. J., Wang C. G., Han S. J., Li M. H. (2012) – Non-linear response of stomata in Pinus koraiensis to tree age and elevation – Trees 26: 1389–1396 – doi:10.1007/s00468-012-0713-8 –
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.17157 – https://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.15.00466 – https://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.1919722117 – https://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.2020.08.012 – https://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 L. W., Zhao P., Wang Q., Ni G. Y., Niu J. F., Zhao X. H., Zhang Z. Z., Zhao P. Q., Gao J. G., Huang Y. Q., Gu D. X., Zhang Z. F. (2015) – Stomatal and hydraulic conductance and water use in a eucalypt plantation in Guangxi, southern China – Agricultural and Forest Meteorology 202: 61-68, ISSN 0168-1923 – https://doi.org/10.1016/j.agrformet.2014.12.003 –https://www.sciencedirect.com/science/article/pii/S0168192314003050 – (On our blog : https://plantstomata.wordpress.com/2024/05/04/canopy-stomatal-conductance-gs-was-higher-in-july-than-in-october-and-linearly-decreased-with-the-natural-logarithm-of-the-vapor-pressure-deficit/ )
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
interaction with the environment-perspectives from hormone regulation –
Front. Biol. 7: 96-112 – https://doi.org/10.1007/s11515-012-1193-3 – https://link.springer.com/article/10.1007/s11515-012-1193-3#citeas – (On our blog : https://plantstomata.wordpress.com/2021/03/14/hormone-signaling-networks-in-guard-cells-and-how-the-networks-integrate-environmental-signals-to-plant-physiological-output/ )
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/ )
Zhu M., Jeon B. W., Geng S., Yu Y., Balmant K., Chen S., Assmann S. M. (2016) – Preparation of epidermal peels and guard cell protoplasts for cellular, electrophysiological, and -omics assays of guard cell function – Methods Mol. Biol. 1363: 89–121 – doi: 10.1007/978-1-4939-3115-6_9 – https://pubmed.ncbi.nlm.nih.gov/26577784/ – (On our blog : https://plantstomata.wordpress.com/2023/01/08/preparation-of-epidermal-peels-and-stomatal-guard-cell-protoplasts/ )
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/ )
Zhu M. , Zhang T., Ji W., Silva-Sanchez C., Song W.-y., Assmann S. M., Harmon A. C., Chen S. 2017) – Redox regulation of a guard cell SNF1-related protein kinase in Brassica napus, an oilseed crop – Biochemical Journal 474(15): 2585-2599 – DOI: 10.1042/BCJ20170070 – http://www.biochemj.org/content/474/15/2585 – (On our blog : https://plantstomata.wordpress.com/2018/01/19/bnsnrk2-4-1c-is-redox-regulated-with-potential-roles-in-guard-cell-signal-transduction-in-stomata/ )
Zhu M., Zhou M., Shabala L., Shabala S. (2015) – Linking osmotic adjustment and stomatal characteristics with salinity stress tolerance in contrasting barley accessions – Funct Plant Biol. 42(3): 252–263 – doi: 10.1071/FP14209 – https://pubmed.ncbi.nlm.nih.gov/32480671/ – (On our blog : https://plantstomata.wordpress.com/2023/01/10/increasing-stomata-density-as-an-adaptive-tool-to-optimise-efficiency-of-co2-assimilation-under-moderate-saline-conditions/ )
Zhu M., Zhu N., Song W.-Y., Harmon A. C., Assmann S. M., Chen S. (2014) – Thiol-based redox proteins in abscisic acid and methyl jasmonate signaling in Brassica napus guard cells – Plant J. 78: 491–515 – doi: 10.1111/tpj.12490 – https://www.ncbi.nlm.nih.gov/pubmed/24580573 – (On our blog : https://plantstomata.wordpress.com/2018/07/30/potential-redox-switches-and-a-protein-redox-regulatory-mechanism-in-aba-and-meja-signal-transduction-in-stomata/ )
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:10.1002/2016GL071733 – https://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/ )
Zhu Y., Ge X. M., Wu M. M., Li X., He J. M. (2014) – The role and interactions of cytosolic alkalization and hydrogen peroxide in ultraviolet B-induced stomatal closure in Arabidopsis – Plant Sci. 215–216: 84–90 – doi: 10.1016/j.plantsci.2013.11.010 – https://www.sciencedirect.com/science/article/pii/S0168945213002537 – (On our blog : https://plantstomata.wordpress.com/2018/07/30/cytosolic-alkalization-and-hydrogen-peroxide-in-ultraviolet-b-induced-stomatal-closure/ )
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