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Tagawa T. (1936) – The influence of atmosplieric humidity upon the suction force of the plant shoot, with special reference to the stomatal aperture – Jap. Journ. Bot. 8: 85-94 –

Tagawa T. (1936) – The influence of light on the stomatal opening – Jap. Journ. Bot. 8: 95-112 –

Tagawa T. (1937) – The influence of the temperature of the culture water on the water ahsorption by the root and on the stomatal aperture – Journ. Facul. Agr., Hokkaido Imp. Univ., Sapporo 39: 271-296 – https://eprints.lib.hokudai.ac.jp/dspace/bitstream/2115/12716/1/39%284%29_p271-296.pdf – (On our blog : https://plantstomata.wordpress.com/2022/01/26/stomatal-behaviour-and-changes-in-temperature/ )

Tagawa T. (1938) – Further studies on the influence of the water temperature on the water absorption and the stomatal aperture – Journal of the Faculty of Agriculture, Hokkaido Imperial University 45(1): 1-3 – https://eprints.lib.hokudai.ac.jp/dspace/bitstream/2115/12735/1/45%281%29_p1-33.pdf – (On our blog : https://plantstomata.wordpress.com/2022/01/22/the-variation-of-the-stomatal-aperture-is-due-not-only-to-the-change-of-the-turgor-pressure-of-the-guard-cells-themselves-but-also-passively-to-the-variation-of-the-side-pressure-of-the-epidermal-cel/ )

Taiz L., Zeiger E. (1998) – Plant Physiology, 2nd Edn. Sunderland, MA: Sinauer Associates.

Taiz L., Zeiger E., Moeller I. M., Murphy A. (2015) – Plant Physiology and Development, Sixth Edition – Topic 10.4 – Phytochrome-mediated Responses in Stomata – http://6e.plantphys.net/index.html – (On our blog : https://plantstomata.wordpress.com/2017/11/08/phytochrome-mediated-responses-in-stomata/ )

Takagi K., Tsuboya T., Takahashi H. (1998) -Diurnal hystereses of stomatal and bulk surface conductances in relation to vapor pressure deficit in a cool-temperate wetland – Agric. For. Meteorol. 91: 177–191 –

Takahashi F., Suzuki T., Osakabe Y., Betsuyaku S., Kondo Y., Dohmae N., Fukuda H., Yamaguchi-Shinozaki K., Shinozaki K. (2018) – A small peptide modulates stomatal control via abscisic acid in long-distance signalling – Nature 556: 235–238 – https://www.nature.com/articles/s41586-018-0009-2 – (On our blog : https://plantstomata.wordpress.com/2019/05/31/a-small-peptide-modulates-stomatal-control-via-aba-3/ )

Takahashi S., Monda K., Higaki T., Hashimoto-Sugimoto M., Negi J., Hasezawa S., Iba K. (2017) – Different Effects of Phosphatidylinositol 4-Kinase (PI4K) and 3-Kinase (PI3K) Inhibitors on Stomatal Responses to Environmental Signals – Frontiers in Plant Science – 8: 677 – doi: 10.3389/fpls.2017.00677

Takahashi S., Monda K., Negi J., Konishi F., Ishikawa S., Hashimoto-Sugimoto M., Goto N., Iba K. (2015) – Natural Variation in Stomatal Responses to Environmental Changes among Arabidopsis thaliana Ecotypes – PLoS One 10: e0117449 — https://doi.org/10.1371/journal.pone.0117449 – https://journals.plos.org/plosone/article/related?id=10.1371/journal.pone.0117449 – (On our blog : https://plantstomata.wordpress.com/2018/11/24/differences-between-ecotypes-in-intrinsic-stomatal-response-mechanisms-to-environmental-signals/

Takahashi Y., Bosmans K. C., Hsu P.-K., Paul K., Seitz C. , Yeh C.-Y., Wang Y.-S. , Yarmolinsky D., Sierla M., Vahisalu T.,  McCammon J. A., Kangasjärvi J., Zhang L., Kollist H., Trac T., Schroeder J. I. (2022) – Stomatal CO2/bicarbonate sensor consists of two interacting protein kinases, Raf-like HT1 and non-kinase-activity activity requiring MPK12/MPK4 – Science Advances 8(49): – DOI: 10.1126/sciadv.abq6161https://www.science.org/doi/10.1126/sciadv.abq6161 – (On our blog : https://plantstomata.wordpress.com/2022/12/14/stomatal-co2-bicarbonate-sensor-consists-of-two-interacting-protein-kinases/ )

Takahashi Y., Ebisu Y., Kinoshita T., Doi M., Okuma E., Murata Y., Shimazaki K.-i (2013) – bHLH transcription factors that facilitate K+ uptake during stomatal opening are repressed by abscisic acid through phosphorylation – Sci. Signal. 6, ra48 – doi: 10.1126/scisignal.2003760 – https://www.ncbi.nlm.nih.gov/pubmed/23779086https://hero.epa.gov/hero/index.cfm/reference/details/reference_id/4300409 (On our blog : https://plantstomata.wordpress.com/2018/06/27/aks-family-of-bhlh-transcription-factors-facilitates-stomatal-opening-through-transcription-of-genes/ ) 

Takahashi Y, Ebisu Y, Kinoshita T, Doi M, Okuma E, Murata Y, Shimazaki K. (2013) – bHLH transcription factors that facilitate K+ uptake during stomatal
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Takahashi Y., Ebisu Y., Shimazaki K.-i. (2017) – Reconstitution of abscisic acid signaling from the receptor to DNA via bHLH transcription factors – Plant Physiol 174: 815–822 – https://doi.org/10.1104/pp.16.01825http://www.plantphysiol.org/content/174/2/815 – (On our blog : https://plantstomata.wordpress.com/2019/02/05/aba-signaling-from-the-receptor-to-dna-in-stomata/ )

Takahashi Y., Kinoshita T. (2015) – Stomatal function has an element of hysteresis – New Phytologist 205: 455–457 – http://www.esalq.usp.br/lepse/imgs/conteudo_thumb/Stomatal-function-has-an-element.pdf – (On our blog : https://plantstomata.wordpress.com/2020/12/13/how-does-stomatal-memory-contribute-to-the-physiological-performance-of-plants/ )

Takahashi Y., Kinoshita T., Matsumoto M., Shimazaki K.-i. (2016) – Inhibition of the Arabidopsis bHLH transcription factor by monomerization through abscisic acid-induced phosphorylation – Plant J. 87(6): 559-67 – doi: 10.1111/tpj.13217 – Epub 2016 Jul 19 – https://pubmed.ncbi.nlm.nih.gov/27227462/ – (On our blog : https://plantstomata.wordpress.com/2020/12/13/a-mechanism-that-inhibits-gene-expression-by-phosphorylation-of-a-bhlh-transcription-factor-in-stomata/ )

Takahashi Y., Kinoshita T., Shimazaki K.-i. (2007) – Protein phosphorylation and binding of a 14-3-3 protein in Vicia guard cells in response to ABA – Plant Cell Physiol. 48: 1182–1191 – doi: 10.1093/pcp/pcm093 – https://www.ncbi.nlm.nih.gov/pubmed/17634179 – (On our blog : https://plantstomata.wordpress.com/2018/06/26/61-kda-protein-may-be-a-substrate-for-aapk-and-it-is-located-upstream-of-h2o2-and-ca2-or-on-ca2-independent-signaling-pathways-in-stomata/ )

Takai T., Ohsumi A., San-Oh Y., Laza M. R. C., Kondo M., Yamamoto T., Yano M. (2009) – Detection of a quantitative trait locus controlling carbon isotope discrimination and its contribution to stomatal conductance in japonica rice – Theoretical Applied Genetics 118: 1401–1410 – https://doi.org/10.1007/s00122-009-0990-9https://link.springer.com/article/10.1007/s00122-009-0990-9 – (On our blog : https://plantstomata.wordpress.com/2019/02/06/detection-of-a-quantitative-trait-locus-and-its-contribution-to-stomatal-conductance/ )

Takai T., Yano M., Yamamoto T. (2010) – Canopy temperature on clear and cloudy days can be used to estimate varietal differences in stomatal conductance in rice – Field Crops Research 115: 165–170 – https://doi.org/10.1016/j.fcr.2009.10.019 –https://www.sciencedirect.com/science/article/pii/S0378429009003001 – (On our blog : https://plantstomata.wordpress.com/2019/02/06/infrared-thermography-may-be-a-simple-method-of-evaluating-varietal-differences-in-stomatal-conductance-through-ctd/ )

Takakura T., Goudriaan J., Louwerse W. (1975) – A behaviour model to simulate stomatal resistance – Agricultural Meteorology 15: 393-404 – https://edepot.wur.nl/218538 – (On our blog : https://plantstomata.wordpress.com/2021/10/15/behaviour-model-may-be-good-enough-to-account-for-the-rather-complicated-interrelations-that-govern-the-stomatal-movement/ )

Takanashi S., Kosugi Y., Matsuo N., Tani M., Ohte N. (2006) – Patchy stomatal behavior in broad-leaved trees grown in different habitats – Tree Physiology 26: 1565–1578 – DOI: 10.1093/treephys/26.12.1565 – https://www.researchgate.net/publication/6629959_Patchy_stomatal_behavior_in_broad-leaved_trees_grown_in_different_habitats – (On our blog : https://plantstomata.wordpress.com/2018/12/12/patchy-stomatal-behavior-in-broad-leaved-trees-grown-in-different-habitats/

Takaoka Y., Miyagawa S., Nakamura A., Egoshi S. Tsukiji S., Ueda M. (2020) – Hoechst-tagged Fluorescein Diacetate for the Fluorescence Imaging-based Assessment of Stomatal Dynamics in Arabidopsis thaliana – Sci Rep 10: 5333 – https://doi.org/10.1038/s41598-020-62239-whttps://www.nature.com/articles/s41598-020-62239-w#citeas – (On our blog : https://plantstomata.wordpress.com/2020/07/18/fluorescein-diacetate-for-the-fluorescence-imaging-based-assessment-of-stomatal-dynamics/ )

Takemiya A., Doi A., Yoshida S., Okajima K., Tokutomi S., Shimazaki K. (2016) – Reconstitution of an Initial Step of Phototropin Signaling in Stomatal Guard Cells – Plant Cell Physiol. 57(1):152-159 – doi: 10.1093/pcp/pcv180 – Epub 2015 Dec 26 – PMID: 26707730 – https://pubmed.ncbi.nlm.nih.gov/26707730/ – (On our blog : https://plantstomata.wordpress.com/2023/04/01/an-initial-step-of-phototropin-signaling-in-stomatal-guard-cells-2/)

Takemiya A., Kinoshita T., Asanuma M., Shimazaki K. (2006) – Protein phosphatase 1 positively regulates stomatal opening in response to blue light in Vicia faba – Proc. Natl. Acad. Sci. USA 103: 13549–13554 – https://doi.org/10.1073/pnas.0602503103https://www.pnas.org/content/103/36/13549 – (On our blog : https://plantstomata.wordpress.com/2019/02/06/pp1-functions-downstream-of-phototropins-and-upstream-of-the-h-atpase-in-the-blue-light-signaling-pathway-of-stomata-2/ )

Takemiya A., Shimazaki K.-i. (2010) – Phosphatidic acid inhibits blue light- induced stomatal opening via inhibition of protein phosphatase – Plant Physiol. 153: 1555–1562 – https://doi.org/10.1104/pp.110.155689 – http://www.plantphysiol.org/content/153/4/1555 – (On our blog : https://plantstomata.wordpress.com/2018/06/28/pa-inhibits-blue-light-signaling-in-stomata-by-pp1c-inhibition-accelerating-stomatal-closure/ )

Takemiya A, Shimazaki K. (2016) – Arabidopsis phot1 and phot2 phosphorylate BLUS1 kinase with different efficiencies in stomatal opening – J Plant Res. 129(2): 167-174 – doi: 10.1007/s10265-015-0780-1 – Epub 2016 Jan 16 – PMID: 26780063 – https://pubmed.ncbi.nlm.nih.gov/26780063/ – (On our blog : https://plantstomata.wordpress.com/2023/04/01/phot1-and-phot2-phosphorylate-blue-light-signaling1-blus1-kinase-as-a-common-substrate-in-stomatal-opening/ )

Takemiya A., Sugiyama N., Fujimoto H., Tsutsumi T., Yamauchi S., Hiyama A., Tada Y., Christie J. M., Shimazaki K.-i. (2013) – Phosphorylation of BLUS1 kinase by phototropins is a primary step in stomatal opening – Nat Commun4: 2094  -DOI: 10.1038/ncomms3094 – https://www.ncbi.nlm.nih.gov/pubmed/23811955 – (On our blog : https://plantstomata.wordpress.com/2018/06/27/blus1-functions-as-a-phototropin-substrate-and-primary-regulator-of-stomatal-control-2/

Takemiya A., Yamauchi S., Yano,T., Ariyoshi C., Shimazaki K. (2013) – Identification of a regulatory subunit of protein phosphatase 1 which mediates blue light signaling for stomatal opening – Plant Cell Physiol. 54: 24–35 – doi: 10.1093/pcp/pcs073 – https://www.ncbi.nlm.nih.gov/pubmed/22585556 (On our blog : https://plantstomata.wordpress.com/2018/06/26/prsl1-functions-as-a-regulatory-subunit-of-pp1-and-regulates-blue-light-signaling-in-stomata-2/ )

Takenaka Y. (1943) – On polyploidy and the size of organs, in particular the size of the stomata – Jap. J. Genet 19: 21-45 – https://eurekamag.com/research/013/447/013447629.php – (On our blog : https://plantstomata.wordpress.com/2022/01/07/gigas-characteristics-and-increases-in-stomatal-dimensions-associated-with-chromosome-reduplication/ )

Takeuchi Y., Kondo N. (1988) – Effect of abscisic acid on glucose metabolism in guard cells of Vicia faba L. – Plant Cell Physiology 29: 247–253 – https://doi.org/10.1093/oxfordjournals.pcp.a077488 –https://academic.oup.com/pcp/article-abstract/29/2/247/1811034 – (On our blog : https://plantstomata.wordpress.com/2019/02/10/aba-may-have-two-different-actions-on-stomatal-movement/ )

Takeuchi Y., Kondo N. (1988) – Effect of abscisic acid on cell-wall metabolism in guard cells of Vicia faba L. – Plant Cell Physiology 29: 573–580 – https://doi.org/10.1093/oxfordjournals.pcp.a077531 –https://academic.oup.com/pcp/article-abstract/29/4/573/1814810 – (On our blog : https://plantstomata.wordpress.com/2019/02/10/cell-wall-metabolism-in-the-guard-cells-may-play-a-role-in-the-regulation-of-stomatal-movement/ )

Takuya F., Tatsumi H., Sokabe M. (2008) – Mechano-sensitive channels regulate the stomatal aperture in Vicia faba – Biochemical and Biophysical Research Communications 366: 758–762 – Mechano-sensitive_channels_regulate_the.pdf –  (On our blog : https://plantstomata.wordpress.com/2017/12/14/mechano-sensitive-channels-regulate-the-stomatal-aperture/ )

Tal M. (1966) – Abnormal stomatal behavior in wilty mutants of tomato – Plant Physiol. 41: 1387-1391 – PMCID: PMC550536 – PMID: 16656409 – https://pdfs.semanticscholar.org/22d2/c97f4d7b27da79699f1e3224e5d0992182a0.pdf – (On our blog : https://plantstomata.wordpress.com/2019/06/04/abnormal-stomatal-behavior-in-wilty-mutants-of-tomato/ )

Tal M., Eshel A., Witztum A. (1976) – Abnormal Stomatal Behaviour and Ion Imbalance in Capsicum scabrous diminutive – Journ. Exp. Bot. 27( 100): 953-960 – (On our blog : https://plantstomata.wordpress.com/2021/09/22/abnormal-stomatal-behaviour-in-capsicum-scabrous-diminutive/ )

Tal M., Imber D. (1970) – Abnormal stomatal behaviour and hormonal imbalance in flacca, a wilty mutant of tomato. II. Auxin and abscisic acid like activity – Plant PhysioL. Lancaster 46: 373-376 – DOI: 10.1104/pp.46.3.373https://www.ncbi.nlm.nih.gov/pubmed/16657470 – (On our blog : https://plantstomata.wordpress.com/2019/05/28/abnormal-stomatal-behaviour-ii-auxin-and-abscisic-acid-like-activity/ )

Tal M., Imber D. (1971) – Abnormal stomatal behaviour and hormonal imbalance in flacca, a wilty mutant of tomato. III. Hormonal effects on the water status in the plant – Plant PhysioL. 47(6): 849-850 – PMCID: PMC396785 – PMID: 16657719 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC396785/ – (On our blog : https://plantstomata.wordpress.com/2019/05/28/abnormal-stomatal-behaviour-iii-hormonal-effects-on-the-water-status-in-the-plant/ )

Tal M., Imber D. (1972) – The effect of abscisic acid on stomatal behavior in flacca, a wilty mutant of tomato, in darkness – New Phytol. 71: 81-84 – https://doi.org/10.1111/j.1469-8137.1972.tb04812.xhttps://nph.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-8137.1972.tb04812.x – (On our blog : https://plantstomata.wordpress.com/2019/06/04/the-effect-of-aba-on-stomatal-behavior/ )

Tal M., Imber D., Erez A., Epstein E. (1979) – Abnormal stomatal behaviour and hormonal imbalance in flacca, a wilty mutant of tomato: V. Effect of Abscisic Acid on Indoleacetic Acid Metabolism and Ethylene Evolution – Plant Physiol. 63(6): – DOI: 10.1104/pp.63.6.1044https://www.researchgate.net/publication/24854076_Abnormal_Stomatal_Behavior_and_Hormonal_Imbalance_in_flacca_a_Wilty_Mutant_of_Tomato_V_Effect_of_Abscisic_Acid_on_Indoleacetic_Acid_Metabolism_and_Ethylene_Evolution – (On our blog : https://plantstomata.wordpress.com/2019/05/28/abnormal-stomatal-behaviour-v-effect-of-aba-on-indoleacetic-acid-metabolism-and-ethylene-evolution/ )

Tal M., Imber D., Gardi L. (1974) – Abnormal stomatal behaviour and hormonal imbalance in flacca, a wilty mutant of tomato. Effect of abscisic acid and auxin on stomatal behaviour and peroxidase activity – J. Expo. Bot. 25: 51-60 –

Tal M., Imber D., Itai C. (1970) – Abnormal stomatal behaviour and hormonal imbalance in flacca, a wilty mutant of tomato. I. Root effect and kinetin-like activity – Plant Physiol. 46: 367-372 – https://doi.org/10.1104/pp.46.3.367http://www.plantphysiol.org/content/46/3/367 – (On our blog : https://plantstomata.wordpress.com/2019/05/28/abnormal-stomatal-behaviour-i-root-effect-and-kinetin-like-activity/ )

Tal M. Nevo Y. (1973) – Abnormal stomatal behaviour and root resistance, and hormonal imbalance in three wilty mutants of tomato – Biochem. Genet. 8: 291–300 – https://doi.org/10.1007/BF00486182https://link.springer.com/article/10.1007%2FBF00486182 – (On our blog : https://plantstomata.wordpress.com/2019/06/04/abnormal-stomatal-behaviour/ )

Talbott L. D. (2006) – The Blue–Green Reversibility of the Blue-Light Response of Stomata – Plant Physiology and Development, Sixth Edition (Eds. Taiz L., Zeiger E., Moeller I. M., Murphy A.,© 2015 Sinauer Associates) – http://6e.plantphys.net/essay10.04.html – (On our blog : https://plantstomata.wordpress.com/2017/11/08/blue-light-response-of-stomata/ )

Talbott L. D., Hammad J. W., Harn L. C., Nguyen V. H., Patel J., Zeiger E. (2006) – Reversal by green light of blue light-stimulated stomatal opening in intact, attached leaves of Arabidopsis operates only in the potassium-dependent, morning phase of movement – Plant Cell Physiol. 47: 332–339 – https://doi.org/10.1093/pcp/pci249 –https://academic.oup.com/pcp/article/47/3/332/1922980 – (On our blog : https://plantstomata.wordpress.com/2019/02/10/stomatal-sensitivity-to-green-light-was-observed-only-in-the-morning-coinciding-with-the-use-of-potassium-as-a-guard-cell-osmoticum/ )

Talbott L. D., Nikolova G., Ortiz A., Shmayevich I. J., Zeiger E. (2002) – Green light reversal of blue light-stimulated stomatal opening is found in a wide range of plant species – Am J Bot 89: 366-368 –  https://doi.org/10.3732/ajb.89.2.366 –https://onlinelibrary.wiley.com/doi/full/10.3732/ajb.89.2.366 – (On our blog : https://plantstomata.wordpress.com/2018/12/03/blue-green-reversibility-of-stomatal-opening-is-a-basic-photobiological-property-of-guard-cells/

Talbott L. D., Rahveh E., Zeiger E. (2003) – Relative humidity is a key factor in the acclimation of the stomatal response to CO2 – Journal of Experimental Botany 54: 2141–2147 – https://doi.org/10.1093/jxb/erg215https://academic.oup.com/jxb/article/54/390/2141/606437 – (On our blog : https://plantstomata.wordpress.com/2019/09/10/humidity-regulation-of-stomatal-co2-sensitivity-could-function-as-a-signal-for-promoting-stomatal-opening-under-low-light-low-co2-conditions/ )

Talbott L. D., Shmayevich I. J., Chung Y., Hammad J. W., Zeiger E. (2003) – Blue Light and Phytochrome-Mediated Stomatal Opening in the npq1 and phot1 phot2Mutants of Arabidopsis – Plant Physiology 133: 1522-1529 – https://doi.org/10.1104/pp.103.029587 – http://www.plantphysiol.org/content/133/4/1522 – (On our blog : https://plantstomata.wordpress.com/2018/12/03/blue-light-and-phytochrome-mediated-stomatal-opening/

Talbott L. D., Srivastava A., Zeiger E. (1996) – Stomata from growth-chamber-grown Vicia faba have an enhanced sensitivity to CO2 – Plant, Cell & Environment 19: 1188-1194 – https://doi.org/10.1111/j.1365-3040.1996.tb00434.xhttps://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-3040.1996.tb00434.x – (On our blog : https://plantstomata.wordpress.com/2019/05/11/acclimation-to-environmental-conditions-alters-the-sensitivity-of-stomata-to-co2-2/ )

Talbott L. D., Zeiger E. (1988) – Light quality and osmoregulation in Vicia guard cells: evidence for involvement of three metabolic pathways. – Plant Physiol. 88: 887–895 – doi: 10.1104/pp.88.3.887 – (On our blog : https://plantstomata.wordpress.com/2017/07/19/light-quality-and-osmoregulation-in-stomata/

Talbott L. D., Zeiger, E. (1993) – Sugar and organic acid accumulation in guard cells of Vicia faba in response to red and blue light – Plant Physiol. 102: 1163–1169 – https://doi.org/10.1104/pp.102.4.1163 – http://www.plantphysiol.org/content/102/4/1163 – (On our blog : https://plantstomata.wordpress.com/2018/06/28/light-quality-modulates-alternative-mechanisms-of-osmotic-accumulation-in-stomata-2/ )

Talbott L. D., Zeiger E. (1996) – Central roles for potassium and sucrose in guard-cell osmoregulation – Plant Physiol. 111: 1051–1057 – https://doi.org/10.1104/pp.111.4.1051 – http://www.plantphysiol.org/content/111/4/1051 – (On our blog : https://plantstomata.wordpress.com/2018/06/27/stomatal-osmoregulation-in-intact-leaves-depends-on-at-least-two-different-osmoregulatory-pathways-k-transport-and-sucrose-metabolism/ )

Talbott L. D., Zeiger E. (1998) – The role of sucrose in guard cell osmoregulation – J. Exp. Bot. 49: 329–337 – doi: 10.1093/jexbot/49.suppl_1.329 – https://academic.oup.com/jxb/article/49/Special_Issue/329/507976 – (On our blog : https://plantstomata.wordpress.com/2018/06/26/sucrose-in-stomatal-osmoregulation/ )

Talbott L. D., Zhu J., Han S. W., Zeiger E. (2002) – Phytochrome and blue light-mediated stomatal opening in the orchid, Paphiopedilum – Plant Cell Physiol 43: 639–646 – PMID: 12091717 – https://doi.org/10.1093/pcp/pcf075 – https://www.ncbi.nlm.nih.gov/pubmed/12091717 – (On our blog : https://plantstomata.wordpress.com/2018/12/03/paphiopedilum-stomata-possess-both-a-blue-light-mediated-opening-response-a-novel-phytochrome-mediated-opening-response/

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Tallman G. (2004) – Are diurnal patterns of stomatal movement the result of alternating metabolism of endogenous guard cell ABA and accumulation of ABA delivered to the apoplast around guard cells by transpiration? – J. Exp. Bot. 55: 1963–1976 – doi: 10.1093/jxb/erh212 – https://www.ncbi.nlm.nih.gov/pubmed/15310824 – (On our blog : https://plantstomata.wordpress.com/2018/06/27/a-model-to-reconcile-proposed-cellular-mechanisms-for-guard-cell-signal-transduction-with-patterns-of-stomatal-movements-in-leaves/

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Tanaka Y., Fujii K., Shiraiwa T. (2010)  Variability of Leaf Morphology and Stomatal Conductance in Soybean [Glycine max (L.) Merr.] Cultivars – Crop Science – 50(6): 2525-2532 – doi:10.2135/cropsci2010.02.0058https://dl.sciencesocieties.org/publications/cs/abstracts/50/6/2525 – (On our blog : https://plantstomata.wordpress.com/2017/11/22/stomatal-conductance-in-soybean-glycine-max/ )

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Tang J. W., Bolstad P. V., Ewers B. E., Desai A. R., Davis K. J., Carey E. V. (2006) – Sap flux-upscaled canopy transpiration, stomatalconductance, and water use efficiency in an old growth forestin the Great Lakes region of the United States – Journal of Geophysical Research-Biogeosciences 111: G02009 – doi:10.1029/2005JG000083

Tang Y., Liang N. (2000) – Characterization of the photosynthetic induction response in a Populus species with stomata barely responding to light changes – Tree Physiology 20: 969–976 – https://www.ncbi.nlm.nih.gov/pubmed/11303572 – (On our blog : https://plantstomata.wordpress.com/2018/01/11/photosynthetic-induction-response-with-stomata-barely-responding-to-light-changes/ )

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Tardieu F. (2016)  Too many partners in root–shoot signals. Does hydraulics qualify as the only signal that feeds back over time for reliable stomatal control? – New Phytologist 212(4): 802–804 – DOI: 10.1111/nph.14292http://onlinelibrary.wiley.com/doi/10.1111/nph.14292/abstract . This article is a Commentary on Visentin et al., 212: 954–963 – (On our blog : https://plantstomata.wordpress.com/2016/11/09/hydraulics-and-stomatal-control/ )

Tardieu F., Davies W. J. (1992) – Stomatal response to abscisic acid is a function of current plant water status – Plant Physiol. 98: 540-545 – https://doi.org/10.1104/pp.98.2.540 – https://www.ncbi.nlm.nih.gov/pubmed/16668674 – (On our blog : https://plantstomata.wordpress.com/2018/10/11/epidermal-water-relations-may-act-as-a-modulator-of-the-responses-of-stomata-to-aba-2/ )

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Tardieu F., Katerji N., Bethenod O., Zhang J., Davies W. J. (1991) – Maize stomatal conductance in the field: Its relationship with soil and plant water potentials, mechanical constraints and ABA concentration in the xylem sap – Plant, Cell and Environment 14: 121–126 – https://doi.org/10.1111/j.1365-3040.1991.tb01378.x –https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1365-3040.1991.tb01378.x – (On our blog : https://plantstomata.wordpress.com/2019/02/11/maize-stomatal-conductance-in-the-field/ )

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Tardieu F., Simonneau T. (1998) – Variability among species of stomatal control under fluctuating soil water status and evaporative demand: modelling isohydric and anisohydric behaviours – Journal of Experimental Botany 49: 419–432 – https://doi.org/10.1093/jxb/49.Special_Issue.419 –https://academic.oup.com/jxb/article/49/Special_Issue/419/508002 – (On our blog : https://plantstomata.wordpress.com/2019/02/13/variability-of-stomatal-control-under-fluctuating-soil-water-status-and-evaporative-demand/ )

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Tarkowska J. A., Wierzbicka M., Grzegölka M. (1975) – Development of stomata in Hordeum vulgare L. under the influence of oleander glycosides and colchicine – Acta Societatis Botanicorum Poloniae XLIV(4): 637- 647 – file:///C:/Users/wille/Downloads/5057-10201-1-PB.pdf – (On our blog : https://plantstomata.wordpress.com/2021/10/02/stomata-are-formed-with-a-changed-number-of-guard-cells-or-subsidiary-cells-a-changed-shape-orientation-and-dimension/ )

Tarutani Y., Morimoto T., Sasaki A., Yasuda M., Nakashita H., Yoshida S., Yamaguchi I., Suzuki Y. (2004) – Molecular Characterization of Two Highly Homologous Receptor-like Kinase Genes, RLK902 and RKL1, in Arabidopsis thaliana – Bioscience, Biotechnology, and Biochemistry 68(9): 1935-1941 – DOI: 10.1271/bbb.68.1935https://www.tandfonline.com/doi/abs/10.1271/bbb.68.1935 – (On our blog : https://plantstomata.wordpress.com/2022/01/15/the-rkl1-promoter-activity-was-dominant-in-the-stomata-cells/ )

Tateda C., Obara K., Abe Y., Sekine R., Nekoduka S., Hikage T., Nishihara M., Sekine K.-T., Fujisaki K. (2019) – The Host Stomatal Density Determines Resistance to Septoria gentianae in Japanese Gentian – Molecular Plant-Microbe Interactions MPMI 32(4): – ISSN:0894-0282 – e-ISSN:1943-7706 – https://doi.org/10.1094/MPMI-05-18-0114-Rhttps://apsjournals.apsnet.org/doi/full/10.1094/MPMI-05-18-0114-R – (On our blog : https://plantstomata.wordpress.com/2021/04/25/stomatal-density-on-the-adaxial-leaf-surface-is-one-of-the-major-factors-determining-the-susceptibility-of-gentian-cultivars-to-septoria-gentianae-and-to-confer-septoria-resistance/ )

Tateda C., Obara K., Abe Y., Sekine R., Nekoduka S., Hikage T., Nishihara M., Sekine K.-T., Fujisaki K. (2019) – The Host Stomatal Density Determines Resistance to Septoria gentianae in Japanese Gentian – APS – https://doi.org/10.1094/MPMI-05-18-0114-Rhttps://apsjournals.apsnet.org/doi/10.1094/MPMI-05-18-0114-R – (On our blog : https://plantstomata.wordpress.com/2021/03/25/stomatal-density-control-may-represent-an-effective-strategy-to-confer-septoria-resistance/ )

Tátrai Z. A., Sanoubar R., Pluhár Z., Mancarella S., Orsini F., Gianquinto G. (2015) – Morphological and Physiological Plant Responses to Drought Stress in Thymus citriodorus – International Journal of Agronomy
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Taub D. R., Wang X. (2013) – Chapter 4.04 – Effects of Carbon Dioxide Enrichment on Plants – Reference Module in Earth Systems and Environmental Sciences – Climate Vulnerability – Understanding and Addressing Threats to Essential Resources 4: 35-50 – https://doi.org/10.1016/B978-0-12-384703-4.00404-4https://www.sciencedirect.com/science/article/pii/B9780123847034004044 – (On our blog : https://plantstomata.wordpress.com/2021/08/18/co2-and-stomatal-conductance-2/ )

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Thiel G., Blatt M. R., Fricker M. D., White I. R., Millner P. (1993) – Modulation of K+ channels in Vicia stomatal guard cells by peptide homologs to the auxin‐binding protein C terminus – Proceedings of the National Academy of Sciences, USA 90: 11.493-11.497 – https://doi.org/10.1073/pnas.90.24.11493 –https://www.pnas.org/content/90/24/11493 – (On our blog : https://plantstomata.wordpress.com/2019/02/13/modulation-of-k-channels-in-stomatal-guard-cells-by-peptide-homologs/ )

Thiel G., MacRobbie E. A., Blatt M. R. (1992) – Membrane transport in stomatal guard cells: the importance of voltage control – Journal of Membrance Biology 126: 1-18 – https://doi.org/10.1007/BF00233456https://link.springer.com/article/10.1007/BF00233456 – (On our blog : https://plantstomata.wordpress.com/2019/05/11/voltage-control-and-membrane-transport-in-stomatal-guard-cells/ )

Thiel G., Wolf A. H. (1997) – Operation of K+‐channels in stomatal movement – Trends in Plant Science 2: 339-345 – https://doi.org/10.1016/S1360-1385(97)84621-3https://www.sciencedirect.com/science/article/pii/S1360138597846213 – (On our blog : https://plantstomata.wordpress.com/2019/05/11/k-%e2%80%90channels-in-stomatal-movement/ )

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Thimann K. V., Satler S. (1979) – Relation between senescence and stomatal opening: senescence in darkness. – Proc. Natl. Acad. Sci. U.S.A. 76: 2770–2773 – doi: 10.1073/pnas.76.6.2770 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC383690/ – (On our blog : https://plantstomata.wordpress.com/2018/06/28/a-parallel-between-stomatal-aperture-and-senescence-with-strong-indication-that-the-stomatal-aperture-is-the-causal-factor/ )

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Thimann K. V., Tan Z.-Y., Park J. (1992) – CYCLING OF STOMATAL APERTURE IN LEAVES OF PLANTS WITH CRASSULACEAN ACID METABOLISM UNDER CONSTANT CONDITIONS – American Journal of Botany 79(1): – https://bsapubs.onlinelibrary.wiley.com/action/doSearch?AllField=Stomata&SeriesKey=15372197&startPage=2&pageSize=20 – (On our blog : https://plantstomata.wordpress.com/2022/07/05/senescence-of-these-leaves-is-modified-by-stomatal-aperture/ )

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Thomas D. A. (1970) – The regulation of stomatal aperture in tobacco leaf epidermal strips I. The effect of ions – Aust. J. Biol. Sci. 23: 961–979 – https://doi.org/10.1071/BI9700961http://www.publish.csiro.au/bi/BI9700961 – (On our blog : https://plantstomata.wordpress.com/2019/04/04/the-effect-of-ions-on-the-regulation-of-stomatal-aperture/ )

Thomas D. A. (1970} -The regulation of stomatal aperture in tobacco leaf epidermal strips. II. The effect of ouabain – Aust. J. biol. Sci. 23: 981-989 – https://www.publish.csiro.au/BI/pdf/BI9700981 – (On our blog : https://plantstomata.wordpress.com/2022/12/30/the-k-dependent-light-stimulated-opening-of-stomata-was-found-to-be-rapidly-reduced-by-low-concentrations-of-ouabain-g-strophanthin/ )

Thomas D. A. (1971) – The regulation of stomatal aperture in tobacco leaf epidermal strips. III The effect of ATP – Aust. J. biol. Sci. 24: 689-707 – https://www.publish.csiro.au/bi/pdf/BI9710689 – (On our blog : https://plantstomata.wordpress.com/2021/10/31/the-effect-of-atp-on-stomatal-movements/ )

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Thomas D. S., Eamus D. (2002) – Seasonal patterns of xylem sap pH, xylem [ABA], leaf water potential and stomatal conductance of 6 evergreen and deciduous Australian savanna tree species – Australian Journal of Botany 50: 229-236 https://doi.org/10.1071/BT01045http://www.publish.csiro.au/bt/BT01045 – (On our blog : https://plantstomata.wordpress.com/2019/09/11/changes-in-xylem-sap-ph-and-aba-content-do-occur-seasonally-in-the-wet-dry-tropics-of-australia-and-that-these-changes-influence-stomatal-conductance-in-evergreen-and-semi-deciduous-species/ )

Thomas D. S., Eamus D., Bell D. (1999) – Optimization theory of stomatal behaviour I. A critical evaluation of five methods of calculation – Journal of Experimental Botany 50(332): 385–392 – (On our blog : https://plantstomata.wordpress.com/2021/09/15/five-methods-for-calculating-the-mar-ginal-unit-water-cost-of-plant-carbon-gain-%e2%88%82e-%e2%88%82a-of-leaves-of-two-australian-tropical-tree-species/ )

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Thomas E. (2018) – Plants Also Absorb Mercury – The Talking Democrat April 3, 2018 – https://www.thetalkingdemocrat.com/2018/04/plants-also-absorb-mercury/ – (On our blog : https://plantstomata.wordpress.com/2018/04/04/plants-also-absorb-mercury-through-their-stomata/ )

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Tombesi S., Nardini A., Frioni T., Soccolini M., Zadra C., Farinelli D., Poni S., Palliotti A. (2015) – Stomatal closure is induced by hydraulic signals and maintained by ABA in drought-stressed grapevine – Scientific Reports 5, Article 12449 – https://doi.org/10.1038/srep12449 –https://www.nature.com/articles/srep12449 – (On our blog : https://plantstomata.wordpress.com/2019/04/05/stomatal-closure-is-induced-by-hydraulic-signals-and-maintained-by-aba-in-drought-stressed-grapevine/ )

Tomimatsu H., Sakata T., Fukayama H., Tang Y. (2019) – Short-term effects of high CO2 accelerate photosynthetic induction in Populus koreana × trichocarpa with always-open stomata regardless of phenotypic changes in high CO2 growth conditions – Tree Physiol. 39: 474–483 – doi: 10.1093/treephys/tpy078https://academic.oup.com/treephys/article/39/3/474/5059390 – (On our blog ;https://plantstomata.wordpress.com/2021/11/08/the-acceleration-of-photosynthetic-induction-under-high-co2-environment-was-mainly-contributed-by-a-short-term-co2-effect-rather-than-by-a-long-term-acclimation-effect-when-stomatal-limitati/ )

Tomimatsu H., Sakata T., Fukayama H., Tang Y. (2019) – Short-term effects of high CO2 accelerate photosynthetic induction in Populus koreana × trichocarpa with always-open stomata regardless of phenotypic changes in high CO2 growth conditions – Tree Physiol. 39: 474–483 – doi: 10.1093/treephys/tpy078https://academic.oup.com/treephys/article/39/3/474/5059390 – (On our blog ;https://plantstomata.wordpress.com/2021/11/08/the-acceleration-of-photosynthetic-induction-under-high-co2-environment-was-mainly-contributed-by-a-short-term-co2-effect-rather-than-by-a-long-term-acclimation-effect-when-stomatal-limitati/ )

Tomimatsu H., Sakata T., Fukayama H., Tang Y. (2019) – Short-term effects of high CO2 accelerate photosynthetic induction in Populus koreana × trichocarpa with always-open stomata regardless of phenotypic changes in high CO2 growth conditions – Tree Physiol. 39: 474–483 – doi: 10.1093/treephys/tpy078https://academic.oup.com/treephys/article/39/3/474/5059390 – (On our blog ;https://plantstomata.wordpress.com/2021/11/08/the-acceleration-of-photosynthetic-induction-under-high-co2-environment-was-mainly-contributed-by-a-short-term-co2-effect-rather-than-by-a-long-term-acclimation-effect-when-stomatal-limitati/ )

Tomimatsu H, Tang Y. (2012) – Elevated CO2 differentially affects photosynthetic induction response in two Populus species with different stomatal behavior – Oecologia 169: 869–878 – doi: 10.1007/s00442-012-2256-5https://pubmed.ncbi.nlm.nih.gov/22302511/ – (On our blog : https://plantstomata.wordpress.com/2021/11/08/a-high-co2-environment-can-reduce-both-biochemical-and-stomatal-limitations-of-leaf-carbon-gain-during-the-photosynthetic-induction-process/ )

Tominaga J., Kawamitsu Y. (2015) – Cuticle Affects Calculations of Internal CO2 in Leaves Closing Their Stomata – Plant and Cell Physiology 56(10): 1900–1908 – https://doi.org/10.1093/pcp/pcv109https://academic.oup.com/pcp/article/56/10/1900/2460822 – (On our blog : https://plantstomata.wordpress.com/2020/11/04/86113/ )

Tominaga J., Stinziano J. R., Hanson D. T. (2020) – Minimum conductance in leaves—cuticle, leaky stomata, or water vapor saturation? – bioRxiv – https://doi.org/10.1101/2020.05.28.120634https://www.biorxiv.org/content/10.1101/2020.05.28.120634v1 – (On our blog : https://plantstomata.wordpress.com/2020/08/13/minimum-conductance-in-leaves-cuticle-leaky-stomata-or-water-vapor-saturation/ )

Tominaga M., Kinoshita T., Shimazaki K. (2001) – Guard-cell chloroplasts provide ATP required for H+ pumping in the plasma membrane and stomatal opening – Plant Cell Physiol. 42: 795–802 – https://doi.org/10.1093/pcp/pce101https://academic.oup.com/pcp/article/42/8/795/1828112 – (On our blog :  https://plantstomata.wordpress.com/2018/12/03/gccs-supply-atp-to-the-cytosol-under-rl-and-atp-is-utilized-by-the-plasma-membrane-h-atpase-for-h-pumping-in-stomatal-opening/

Tong L., Feng Z. W., Sudebilige-Wang Q., Geng C. M., Lu F., Wang W., Wang X. K. (2012) – Stomatal ozone uptake modeling and comparative analysis of flux-response relationships of winter wheat – Acta Ecologica Sinica 32: 2890–2899 – [In Chinese with English summary] –

Tong L., Wang X.-k., Sudebilige, 2, Wang Q., Geng C. M., Wang W., Song W-z., Lu F.,1, Liu H.-J., 3, Yin B.-h., 3, Sui L.-h., 4, Feng Z.-w. (2011) – Stomatal ozone uptake modeling and comparative analysis of flux-response relationships of rice – Journal of Agro-Environmental Science 30: 1930–1938 – [In Chinese with English summary] – http://en.cnki.com.cn/Article_en/CJFDTOTAL-NHBH201110005.htm – (On our blog : https://plantstomata.wordpress.com/2019/02/07/stomatal-ozone-uptake-modeling/ )

Tonzig S., Ott-Candella (1946) – L’azione della colchicina sullo svippo degli apparati stomataci – Nueva G. Bot. Ital. (N. S.) 53: 835-847 –

Tooulakou G., Giannopoulos A., Nikolopoulos D., Bresta P., Dotsika E., Orkoula M. G., Kontoyannis C. G., Fasseas C., Liakopoulos G., Klapa M. I., Karabourniotis G. (2016) – Reevaluation of the plant “gemstones”: Calcium oxalate crystals sustain photosynthesis under drought conditions – Science.gov (United States) –https://worldwidescience.org/topicpages/c/closing+plant+stomata.html# – (On our blog : https://plantstomata.wordpress.com/2022/03/06/pigweed-amaranthusis-able-to-photosynthesize-even-under-drought-conditionswhen-stomata-are-closed-and-water-losses-are-limited-using-carbon-dioxide-from-crystal-decomposition-i/ )

Torii K. U. (2006) – Communication, fate, and decision making during stomatal development – Journal of the Society of Japanese Women Scientists 7: 12-17 –

Torii K. U. (2006) – Stomatal patterning and differentiation in plants: Emerging roles of cell-cell signaling – Tanpakushitsu Kakusan Koso 51(2):145-154 – In Japanese – PMID: 16457206 –

Torii K. U. (2007) – Giving Voice to Stomata Differentiation – Cell 128(3): 419 – https://doi.org/10.1016/j.cell.2007.01.025https://www.cell.com/cell/fulltext/S0092-8674(07)00123-7?_returnURL=https%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS0092867407001237%3Fshowall%3Dtrue – (On our blog : https://plantstomata.wordpress.com/2022/01/30/stomata-differentiation/ )

Torii K. U. (2007) – Stomatal patterning and guard cell differentiation – In: Cell Division Control in Plants – Plant Cell Monograph (9) Eds. by D.P.S.Verma and Z. Hong. Springer-Verlag, 343-359 – DOI:  10.1007/7089_2007_135https://www.researchgate.net/publication/225829006_Stomatal_Patterning_and_Guard_Cell_Differentiation – (On our blog : https://plantstomata.wordpress.com/2022/12/30/cell-state-transition-events-leading-to-stomatal-guard-cell-differentiation-and-cell-cell-signaling-mechanisms-controlling-stomatal-patterning/ )

Torii K. U. (2012) – Cell-cell-communication and stomatal patterning – 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/stomatal-patterning-and-differentiation/ )

Torii K. U. (2012) – Chemical signal helps plants control their “breathing” – HomeBiologyBiotechnology 2012 – https://phys.org/news/2012-01-chemical.html – (On our blog : https://plantstomata.wordpress.com/2019/02/08/chemical-signal-helps-plants-control-their-breathing/ )

Torii K. U. (2012) – Mix-and-match: ligand-receptor pairs in stomatal development and beyond – Trends Plant Sci. 17(12): 711-719 – doi: 10.1016/j.tplants.2012.06.013 – Epub 2012 Jul 21 – https://www.ncbi.nlm.nih.gov/pubmed/22819466 – (On our blog : https://plantstomata.wordpress.com/2019/09/07/ligand-receptor-pairs-in-stomatal-development-and-beyond/ )

Torii K. U. (2015) – Stomatal differentiation: the beginning and the end – Curr. Opin. Plant Biol. 28: 16–22 – doi: 10.1016/j.pbi.2015.08.005 – https://www.infona.pl/resource/bwmeta1.element.elsevier-cc2b73be-b5a3-3aee-a460-2d28ab3581a9 – (On our blog : https://plantstomata.wordpress.com/2017/10/09/the-beginning-and-the-end-of-stomatal-differentiation/ )

Torii K. U. (2021) – Stomatal Development in the Context of Epidermal Tissues – Annals of Botany – 128: 137-148 – PMID: 33877316 – DOI: 10.1093/aob/mcab052file:///C:/Users/wille/Downloads/Stomatal_Development_in_the_Context_of_Epidermal_T.pdf – (On our blog : https://plantstomata.wordpress.com/2021/06/04/stomatal-development-in-the-context-of-epidermal-tissues/ )

Torii Lab (xxxx) – The Mechanisms of Stomatal Development – Torii Laboratory – https://www.plant-stomata.org/stomatal-development – (On our blog : https://plantstomata.wordpress.com/2022/05/01/stomatal-development-4/ )

Torii Lab (2012) – Research 1 – Stomatal development – http://faculty.washington.edu/ktorii/stomata.html – (On our blog : https://plantstomata.wordpress.com/2017/11/08/stomatal-development-torii-lab/ )

Torii Lab (2012) – Research 2 – Cell-Cell Communication and Stomatal Patterning – https://faculty.washington.edu/ktorii/stomata2.html – (On our blog : https://plantstomata.wordpress.com/2021/02/21/cell-cell-communication-and-stomatal-patterning/ )

Torii Lab (2012) – Research 3 – A Trio of ‘Key Switch’ Genes Directing Stomatal Differentiation – https://faculty.washington.edu/ktorii/index.html – (On our blog : https://plantstomata.wordpress.com/2021/02/21/88295/ )

Torii Lab (2012) – Research 4 – Peptide ligands specifying stomatal patterning – https://faculty.washington.edu/ktorii/stomata4.html – (On our blog : https://plantstomata.wordpress.com/2021/02/21/comparative-studies-of-stomatal-patterning-might-unravel-the-underlying-molecular-basis-of-the-evolution-and-diversity-of-stomatal-patterning/ )

Torii K. U., Kanaoka M. M., Pillitteri L. J., Bogenschutz N. L. (2007) – Stomatal development: Three steps for cell-type differentiation – Plant Signaling & Behavior 2: 311-313 – PMID: 19704632 – PMCID: PMC2634161 – DOI: 10.4161/psb.2.4.4072https://pubmed.ncbi.nlm.nih.gov/19704632/ – (On our blog : https://plantstomata.wordpress.com/2022/12/30/a-three-step-relay-of-the-three-bhlhs-establishes-the-molecular-framework-for-stomatal-differentiation/ )

Torralbo F., González-Moro M. B., Baroja-Fernández E., Aranjuelo I., González-Murua C. (2019) – Differential Regulation of Stomatal Conductance as a Strategy to Cope With Ammonium Fertilizer Under Ambient Versus Elevated CO2 – Front Plant Sci. 10: 597 – doi: 10.3389/fpls.2019.00597 -eCollection 2019 – https://www.ncbi.nlm.nih.gov/pubmed/31178873 – (On our blog : https://plantstomata.wordpress.com/2019/09/08/differential-regulation-of-stomatal-conductance/ )

Torre S., Fjeld T., Gislerod H. R., Moe R. (2003) – Leaf anatomy and stomatal morphology of greenhouse roses grown at moderate or high air humidity – J. Amer. Hort. Sci. 128(4): 598-602 – http://journal.ashspublications.org/content/128/4/598.full.pdf – (On our blog : https://plantstomata.wordpress.com/2017/12/21/65132/ )

Torrecillas A., Ruiz-Sanchez M. C., Leon A., Garcia A. L. (1988) – Stomatal response to leaf water potential in almond trees under drip irrigated and non irrigated conditions – Plant Soil 112: 151- 153 – https://doi.org/10.1007/BF02181765https://link.springer.com/article/10.1007/BF02181765 – (On our blog : https://plantstomata.wordpress.com/2019/02/07/stomatal-response-to-leaf-water-potential/ )

Torres‐Ruiz J. M., Diaz‐Espejo A., Morales‐Sillero A., Martín‐ Palomo M. J., Mayr S., Beikircher B., Fernandez J. E. (2013) – Shoot hydraulic characteristics, plant water status and stomatal response in olive trees under different soil water conditions – Plant Soil 373: 77–87 – https://doi.org/10.1007/s11104-013-1774-1https://link.springer.com/article/10.1007/s11104-013-1774-1 – (On our blog : https://plantstomata.wordpress.com/2019/02/07/stomatal-response-in-olive-trees-under-different-soil-water-conditions/ )

Torres‐Ruiz J. M., Diaz‐Espejo A., Perez-Martin A., Hernandez-Santana V. (2015) – Role of hydraulic and chemical signals in leaves, stems and roots in the stomatal behaviour of olive trees under water stress and recovery conditions – Tree Physiol. 35(4): 415-424 – doi: 10.1093/treephys/tpu055 – Epub 2014 Jul 15 – https://pubmed.ncbi.nlm.nih.gov/25030936/ – (On our blog : https://plantstomata.wordpress.com/2020/07/15/role-of-hydraulic-and-chemical-signals-in-leaves-stems-and-roots-in-the-stomatal-behaviour/ )

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Tossi V., Lamattina L., Jenkins G. I., Cassia R. O. (2014) – Ultraviolet-B-induced stomatal closure in Arabidopsis is regulated by the UV RESISTANCE LOCUS8 photoreceptor in a nitric oxide-dependent mechanism – Plant Physiol. 164: 2220–2230 – https://doi.org/10.1104/pp.113.231753http://www.plantphysiol.org/content/164/4/2220?ijkey=9cbe07ae01485281372ca65fb986d746702ec4d6&keytype2=tf_ipsecsha – (On our blog : https://plantstomata.wordpress.com/2019/10/04/the-uvr8-pathway-regulates-stomatal-closure-by-a-mechanism-involving-both-h2o2-and-no-generation-in-response-to-uv-b-exposure/ )

Toum L., Torres P. S., Gallego S. M., Benavídes M. P., Vojnov A. A., Gudesblat G. E. (2016) – Coronatine Inhibits Stomatal Closure through Guard Cell-Specific Inhibition of NADPH Oxidase-Dependent ROS Production – Front Plant Sci. 7: 1851 – doi: 10.3389/fpls.2016.01851 – eCollection 2016 – https://www.ncbi.nlm.nih.gov/pubmed/28018388 – (On lour blog : https://plantstomata.wordpress.com/2019/09/09/inhibition-of-nadph-oxidase-dependent-ros-synthesis-in-stomatal-guard-cells-plays-an-important-role-during-endophytic-colonization-by-pst-through-stomata/ )

Trafton A. (2017) – Sensors applied to plant leaves warn of water shortage – http://news.mit.edu/2017/sensors-applied-plant-leaves-warn-water-shortage-1108 – (On our blog : https://plantstomata.wordpress.com/2017/11/08/monitoring-stomatal-movements-continuously/ )

Travis A. J., Mansfield T. A. (1977) – Studies of malate formation in isolated guard cells – New Phytol 78: 541-546 – https://doi.org/10.1111/j.1469-8137.1977.tb02157.x – https://nph.onlinelibrary.wiley.com/doi/10.1111/j.1469-8137.1977.tb02157.x – (On our blog : https://plantstomata.wordpress.com/2019/02/12/carboxylation-of-phosphenolpyruvate-plays-no-major-part-in-the-formation-of-malate-in-stomata/ )

Travis A. J., Mansfield T. A. (1979) – Reversal of CO2 responses of stomata by fusicoccin – New Phytol. 83: 607-614 – http://onlinelibrary.wiley.com/doi/10.1111/j.1469-8137.1979.tb02292.x/full –https://plantstomata.wordpress.com/2017/07/16/fusicoccin-and-the-reversal-of-the-co2-responses-of-stomata/ )

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Travis A. J., Mansfield T. A. (1981) – Light saturation of stomatal opening on the adaxial and abaxial epidermis of Commelina communis – J Exp Bot 32: 1169–1179 – https://doi.org/10.1093/jxb/32.6.1169https://academic.oup.com/jxb/article-abstract/32/6/1169/486455?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2019/01/11/stomata-on-the-abaxial-epidermis-were-considerably-more-sensitive-to-light-than-those-on-the-adaxial-epidermis/ )

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Trejo C. L., Davies W. J. (1991) – Drought-induced closure of Phaseolus vulgaris L. stomata precedes leaf water deficit and any increase in xylem ABA concentration – J. Exp. Bot. 42: 1507-1515 – PMID: 12228634 PMCID: PMC161380 – https://doi.org/10.1093/jxb/42.12.1507 –https://academic.oup.com/jxb/article-abstract/42/12/1507/603882?redirectedFrom=PDF – (On our blog : https://plantstomata.wordpress.com/2019/02/08/an-as-yet-unidentified-regulator-of-stomatal-behaviour/ )

Trejo C. L., Davies W. J., Ruiz L. P. (1993) – Sensitivity of stomata to abscisic acid. An effect of the mesophyll – Plant Physiol. 102: 497–502 –  PMID: 12231838 PMCID: PMC158804 – https://www.ncbi.nlm.nih.gov/pubmed/12231838?dopt=Abstract – (On our blog : https://plantstomata.wordpress.com/2018/10/11/an-important-role-for-aba-metabolism-in-the-regulation-of-stomatal-behavior/ )

Triboulot M. B., Fauveau M. L., Breda N., Label P., Dreyer E. (1996)  – Stomatal conductance and xylem-sap abscisic acid (ABA) in adult oak trees during a gradually imposed drought – Annals of Forest Science 53: 207–220 – DOI: 10.1051/forest:19960204 – https://www.afs-journal.org/articles/forest/abs/1996/02/AFS_0003-4312_1996_53_2-3_ART0004/AFS_0003-4312_1996_53_2-3_ART0004.html – (On our blog : https://plantstomata.wordpress.com/2018/11/01/stomatal-conductance-and-xylem-sap-aba-during-a-gradually-imposed-drought/ )

Tricker P. J., Gibbings J. G., Rodriguez Lopez C. M., Hadley P., Wilkinson M. J. (2012) – Low relative humidity triggers RNA-directed de novo DNA methylation and suppression of genes controlling stomatal development – J. Exp. Bot. 63:  3799–3813 – DOI:  10.1093/jxb/ers076 –  https://www.ncbi.nlm.nih.gov/pubmed/22442411 – (On our blog : https://plantstomata.wordpress.com/2019/02/08/epigenetic-regulation-of-stomatal-development/ )

Tricker P. J., Trewin H., Kull O., Clarkson G. J. J., Eensalu E., Tallis M. J., Colella A., Doncaster C. P., Sabatti M., Taylor G. (2005) – Stomatal conductance and not stomatal density determines the long-term reduction in leaf transpiration of poplar in elevated CO2 – Oecologia 143: 652–660 – DOI: 10.1007/s00442-005-0025-4Stomatal_conductance_and_not_stomatal_de.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/20/altered-cuticular-development-during-canopy-closure-may-partially-explain-the-changing-response-of-stomata-to-elevated-co2/ )

Triviño M., Martín-Trillo M., Ballesteros I., Delgado D., De Marcos A., Desvoyes B., Gutiérrez C., Mena M., Fenoll C. (2013) – Timely expression of the Arabidopsis stoma-fate master regulator MUTE is required for specification of other epidermal cell types – Plant J. 75: 808–822 – DOI:  10.1111/tpj.12244 – https://www.ncbi.nlm.nih.gov/pubmed/23662679 – (On our blog : https://plantstomata.wordpress.com/2019/02/08/timely-mute-expression-is-essential-to-prevent-stomatal-fate-in-slgcs-and-to-promote-their-differentiation-as-pavement-cells-2/ )

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Tsai H.-J., Shao K.-H., Chan M.-T., Cheng C.-O., Yeh K.-W., Oelmüller R., Wang S.-J. (2020)Piriformospora indica symbiosis improves water stress tolerance of rice through regulating stomata behavior and ROS scavenging systems – Plant Signaling & Behavior 15(2): – https://doi.org/10.1080/15592324.2020.1722447https://www.tandfonline.com/doi/abs/10.1080/15592324.2020.1722447?scroll=top&needAccess=true&journalCode=kpsb20 – (On our blog : https://plantstomata.wordpress.com/2020/05/14/piriformospora-indica-promotes-rice-performance-under-water-stress-by-stomata-closure/ )

Tsai M.-Y., Kuan C., Guo Z.-L., Yang H.-A., Chung K.-F., Ho C.-M. K. (2022) – Stomatal clustering in Begonia improves water use efficiency by modulating stomatal movement and leaf structure – Plant-Environment Interactions 3(4): 141-154 – https://doi.org/10.1002/pei3.10086https://onlinelibrary.wiley.com/doi/full/10.1002/pei3.10086 – (On our blog : https://plantstomata.wordpress.com/2022/09/20/tight-support-between-stomatal-development-and-environmental-adaption/ )

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Tucker D. T. (2017) – Stanford study shows U.S. grasslands affected more by atmospheric dryness than precipitation – Stanford News Service – https://news.stanford.edu/press-releases/2017/03/06/u-s-grasslands-ated-dry-air-rain/ – (On our blog : https://plantstomata.wordpress.com/2018/11/27/conditions-under-which-plants-in-u-s-grasslands-open-and-close-their-stomata/

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Tupitsyn N. V., Zakharov V. G. (1996) – Inheritance of the stomatal length on the plate of the first leaf of shoots – Dokl. Ross. Akad. S-Kh. Nauk, 1996(2): 9–12 –

Tupitsyn N. V., Zakharov V. G. (1996) – Inheritance of the stomatal length of the first leaf blade of sprouts – Russian Agricultural Sciences 3: 13-17 – https://eurekamag.com/research/002/873/002873866.php – (On our blog : https://plantstomata.wordpress.com/2022/01/13/stomatal-length-of-the-first-leaf-blade-of-wheat-seedlings/ )

Turan M. A., Elkarim A. H. A., Taban N., Taban S. (2009) – Effect of salt stress on growth, stomatal resistance, proline and chlorophyll concentrations on maize plant – African Journal of Agricultural Research 4(9): 893-897 – ISSN 1991-637X – https://www.researchgate.net/publication/228878906_Effect_of_salt_stress_on_growth_stomatal_resistance_proline_and_chlorophyll_concentrations_on_maize_plant – (On our blog : https://plantstomata.wordpress.com/2022/12/30/effect-of-salt-stress-on-growth-and-stomatal-resistance/ )

Turan M. A., Katkat V., Taban S. (2007) – Variations in proline, chlorophyll and mineral elements contents of wheat plants grown under salinity stress – J. Agron. 6: 137-141 – DOI: 10.3923/ja.2007.137.141https://scialert.net/abstract/?doi=ja.2007.137.141 – (On our blog : https://plantstomata.wordpress.com/2022/12/30/stomata-and-salinity-stress/ )

Turan M. A., Katkat V., Taban S. (2007) – Salinity-induced stomatal resistance, proline, chlorophyll and ion concentrations of bean – Int. J. Agric. Res. 2: 483-488 – DOI: 10.3923/ijar.2007.483.488https://scialert.net/abstract/?doi=ijar.2007.483.488 – (On our blog : https://plantstomata.wordpress.com/2022/12/30/while-stomatal-resistance-proline-na-and-cl-concentrations-of-plants-were-increased-by-high-salinity-total-chlorophyll-and-k-concentrations-were-decreased/ )

Turan M. A., Turkmen N., Taban N. (2007) – Effect of NaCl on Stomatal Resistance and Proline, Chlorophyll, Na, Cl and K Concentrations of Lentil Plants – Journal of Agronomy 6: 378-381 – DOI: 10.3923/ja.2007.378.381https://scialert.net/abstract/?doi=ja.2007.378.381 – (On our blog : https://plantstomata.wordpress.com/2021/12/25/stomatal-resistance-and-concentrations-of-proline-na-and-cl-were-increased-by-treatment-with-nacl/ )

Turnbull M. H., Whitehead D., Tissue D. T., Schuster W. S., Brown K. J., Engel V. C., Griffin K. L. (2002) – Photosynthetic characteristics in canopies of Quercus rubra, Quercus prinus and Acer rubrum differ in response to soil water availability – Oecologia 130(4): 515-524 – doi: 10.1007/s00442-001-0842-z – Epub 2002 Feb 1 – https://www.ncbi.nlm.nih.gov/pubmed/28547252 – (On our blog : https://plantstomata.wordpress.com/2019/08/31/stomatal-behavior-and-photosynthetic-characteristics-in-canopies-differ-in-response-to-soil-water-availability/ )

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Turner N. C. (1969) – Stomatal Resistance to Transpiration in Three Contrasting Canopies – Crop Science 9(3): – https://doi.org/10.2135/cropsci1969.0011183X000900030015xhttps://acsess.onlinelibrary.wiley.com/doi/abs/10.2135/cropsci1969.0011183X000900030015x – (On our blog : https://plantstomata.wordpress.com/2020/06/01/stomatal-resistance-to-transpiration/ )

Turner N. C. (1970) – Response of adaxial and abaxial stomata to light – New Phytologist 69: 647-653 – https://www.jstor.org/stable/2430521https://www.jstor.org/stable/2430521?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2019/05/11/response-of-adaxial-and-abaxial-stomata-to-light/ )

Turner N. C. (1972) – STOMATAL BEHAVIOR OF AVENA SATIVA TREATED WITH TWO PHYTOTOXINS, VICTORIN AND FUSICOCCIN – American Journal of Botany 59(2): – https://bsapubs.onlinelibrary.wiley.com/action/doSearch?AllField=Stomata&SeriesKey=15372197&startPage=2&pageSize=20 – (On our blog : https://plantstomata.wordpress.com/2022/07/05/victorin-and-fusicoccin-differ-in-their-effects-on-the-guard-cells/ )

Turner N. C. (1972) – Fusicoccin–a phytotoxin that opens stomata – Phytotoxins in Plant Diseases; Proceedings of the NATO Advanced Study Institute : 399-402 – https://agris.fao.org/agris-search/search.do?recordID=US201302311644

Turner N. C. (1972) – K+ uptake by guard cells stimulated by fusicoccin – Nature 235: 341-342 – DOI: 10.1038/235341a0 – http://adsabs.harvard.edu/abs/1972Natur.235..341T – (On our blog : https://plantstomata.wordpress.com/2019/02/12/accumulation-of-potassium-in-stomata-during-opening-in-darkness/ )

Turner N. C. (1973) – Action of fusicoccin on the potassium balance of guard cells of Phaseolus vulgaris – Amer. J. Bot. 60(7): 717-725 – DOI: 10.1002/j.1537-2197.1973.tb05978.x – https://www.researchgate.net/publication/322829146_ACTION_OF_FUSICOCCIN_ON_THE_POTASSIUM_BALANCE_OF_GUARD_CELLS_OF_PHASEOLUS_VULGARIS – (On our blog : https://plantstomata.wordpress.com/2018/11/12/action-of-fusicoccin-on-the-potassium-balance-of-stomatal-guard-cells/ )

Turner N. C. (1974) – Stomatal Behavior and Water Status of Maize, Sorghum, and Tobacco under Field Conditions II. At Low Soil Water Potential – PMCID: PMC543223 – PMID: 16658706 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC543223/ – (On our blog : https://plantstomata.wordpress.com/2019/02/13/stomatal-behavior-at-low-soil-water-potential/ )

Turner N. C. (1974) – Stomatal responses to light and water under field conditions – In R. Bieleski (Ed.), mechanisms of Regulation of Plant Growth, Bulletin 12: 423-432 – Royal Society of New Zealand

Turner N. C. (1975) – Concurrent comparisons of stomatal behavior, water status, and evaporation of maize in soil at high or low water potential – Plant Physiol. 55(5): 932-936 – DOI:10.1104/PP.55.5.932https://www.semanticscholar.org/paper/Concurrent-comparisons-of-stomatal-behavior%2C-water-Turner/42be46261e5ea45e16be3cb5b3fe1c21f9c22c5f – (On our blog : https://plantstomata.wordpress.com/2021/09/25/93679/ )

Turner N. C. (1979) – Differences in response of adaxial and abaxial stomata to environmental variables. In “Structure, Function and Ecology of Stomata” (D. S. Sen, D. D. Chawan and R. P. Bansal, eds), 229-250 – Bishen Singh, Mahendra Pal Singh, Dehra Dun. –

Turner N. C. (1991) – Measurement and influence of environmental and plant factors on stomatal conductance in the field – Agricultural and Forest Meteorology 54(2–4): 137-154 – https://doi.org/10.1016/0168-1923(91)90003-9https://www.sciencedirect.com/science/article/abs/pii/0168192391900039 – (On our blog : https://plantstomata.wordpress.com/2021/05/15/the-implications-of-environmental-and-plant-factors-on-the-measured-values-of-stomatal-conductance/ )

Turner N. C., Begg J. E. (1973) – Stomatal behaviour and water status of maize, sorghum and tobacco under field conditions. I. At high water potential – Plant Physiol. 51: 31-36 – http://www.plantphysiol.org/content/plantphysiol/51/1/31.full.pdf – (On our blog : https://plantstomata.wordpress.com/2019/02/13/stomatal-behaviour-at-high-water-potential/ )

Turner N. C., Begg J. E., Tonnet M. L. (1978) – Osmotic adjustment of sorghum and sunflower crops in response to water deficits and its influence on the water potential at which stomata close – Australian Journ. Plant Physiology 5: 597-608 – https://doi.org/10.1071/PP9780597http://www.publish.csiro.au/FP/PP9780597 – (On our blog : https://plantstomata.wordpress.com/2019/05/11/osmotic-adjustment-in-response-to-water-deficits-and-its-influence-on-the-water-potential-at-which-stomata-close/ )

Turner N. C., Graniti A. (1969) – Fusicoccin: a fungal toxin that opens stomata – Nature 223: 1070–1071 – doi: 10.1038/2231070a0https://www.nature.com/articles/2231070a0 – (On our blog : https://plantstomata.wordpress.com/2019/05/28/fusicoccin-a-fungal-toxin-that-opens-stomata/ )

Turner N. C., Heichel G. H. (1977) – Stomatal development and seasonal changes in diffusive resistance of primary and regrowth foliage of red oak (Quercus rubra L) and red maple (Acen rabrum L) – New Phytol 78: 71–81 – https://doi.org/10.1111/j.1469-8137.1977.tb01544.x – https://nph.onlinelibrary.wiley.com/doi/abs/  – (On our blog : https://plantstomata.wordpress.com/2019/02/14/the-development-of-light-sensitivity-was-strongly-dependent-on-environmental-regulation-of-stomatal-metabolism/ )

Turner N. C., Incoll L. D. (1972) – The vertical distribution of photosynthesis in crops of tobacco and sorghum – Journal of Applied Ecology – Published online 19 Dec 1972 – DOI: 10.2307/2402894https://www.britishecologicalsociety.org/applied-ecology-resources/document/19721702630/ – (On our blog : https://plantstomata.wordpress.com/2021/10/22/stomata-and-vertical-distribution-of-photosynthesis-in-crops/ )

Turner N. C., O’Toole J. C., Cruz R. Z., Yambao E. B., Ahmad S., Namuco O. S., Dingkuhn M. (1986) – Responses of seven diverse rice cultivars to water deficits. II. Osmotic adjustment, leaf elasticity, leaf extension, leaf death, stomatal conductance and photosynthesis – Field Crop Res. 13: 273–286 – doi: 10.1016/0378-4290(86)90028-6https://www.sciencedirect.com/science/article/pii/0378429086900286 – (On our blog : https://plantstomata.wordpress.com/2019/02/14/osmotic-adjustment-leaf-elasticity-leaf-extension-leaf-death-stomatal-conductance-and-photosynthesis/ )

Turner N. C., Rich S., Tomlinson H. (1972) – Stomatal conductance, fleck injury and growth of tobacco cultivars varying in ozone tolerance – Phytopathology 62: 63-67 – https://www.apsnet.org/publications/phytopathology/backissues/Documents/1972Articles/Phyto62n01_63.PDF – (On our blog : https://plantstomata.wordpress.com/2021/11/13/stomatal-conductance-and-frequency/ )

Turner N. C., Schulze E.-D., Gollan T. (1984) – The response of stomata and leaf gas exchange to vapor pressure deficits and soil water content. I. Species comparison at high soil water contents – Oecologia 63: 338-342 – https://link.springer.com/article/10.1007%2FBF00390662 – (On our blog :  https://plantstomata.wordpress.com/2017/07/16/the-response-of-stomata-to-vapor-pressure-deficits-and-soil-water-content/

Turner N. C., Schulze E.-D., Gollan T. (1985) – The responses of stomata and leaf gas exchange to vapor pressure deficits and soil water content. II. In the mesophytic herbaceous species Helianthus annuus – Oecologia 65: 348-355 – doi: 10.1007/BF00378908 – https://www.ncbi.nlm.nih.gov/pubmed/2 – (On our blog : https://plantstomata.wordpress.com/2018/12/13/soil-water-status-not-leaf-water-status-affects-the-stomatal-behaviour-and-photosynthesis/

Turner N. C., Singh D. P. (1984) – Responses of adaxial and abaxial stomata to light and water deficits in sunflower and sorghum – New Phytologist 96: 187-193 –  https://nph.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1469-8137.1984.tb03555.x – (On our blog : https://plantstomata.wordpress.com/2019/05/11/responses-of-adaxial-and-abaxial-stomata-to-light-and-water-deficits/ )

Turner N. C., Waggoner P. E. (1968) – Effects of changing stomatal widths in a red pine forest on soil water content, leaf water potential, bole diameter and growth – Plant Physiol. 43 : 973-978 – doi: 10.1104/pp.43.6.973https://pubmed.ncbi.nlm.nih.gov/16656870/ – (On our blog : https://plantstomata.wordpress.com/2022/12/30/changing-stomatal-widths/ )

Turrell F. M. (1947) – Citrus leaf stomata, structure, composition, and pore size in relation to penetration of liquids – Bot. Gaz. 108: 476-483 –http://www.journals.uchicago.edu/doi/abs/10.1086/335435 – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/64420 )

Turrell F. M., Klotz L. J. (xxxx) –  Density of Stomata and Oil Glands and Incidence of Water Spot in the Rind of Washington Navel Orange – Botanical Gazette 101(4): – https://www.journals.uchicago.edu/doi/pdf/10.1086/334920 – (On our blog : https://plantstomata.wordpress.com/2021/04/17/stomata-in-the-rind-of-washington-navel-orange/ )

Turunen M., Huttunen S. (1990) – A Review of the Response of Epicuticular Wax of Conifer Needles to Air Pollution – Journal of Environmental Quality 19(1): 35-45 – https://doi.org/10.2134/jeq1990.00472425001900010003x https://acsess.onlinelibrary.wiley.com/doi/abs/10.2134/jeq1990.00472425001900010003x – (On our blog : https://plantstomata.wordpress.com/2021/08/22/increased-or-decreased-stomatal-and-cuticular-diffusion-resistance-of-the-needles-leads-to-altered-transpiration-rates/ )

Turunen M., Huttunen S. (1991) – Effect of simulated acid rain on the epicuticular wax of Scots pine needles under northerly conditions – Canadian Journal of Botany 69(2): 412-419 – https://doi.org/10.1139/b91-057https://cdnsciencepub.com/doi/abs/10.1139/b91-057?journalCode=cjb1 – (On our blog : https://plantstomata.wordpress.com/2021/05/17/four-types-of-deformed-stomatal-complex-namely-narrow-half-formed-occluded-and-double-sized-were-found/ )

TutorVista (2010) – Video: Structure And Working Of Stomata – https://www.youtube.com/watch?v=IlmgFYmbAUg – (On our blog : https://plantstomata.wordpress.com/2017/11/10/video-on-stomata/ )

Tuzet A., Perrier A., Leuning R. A. (2003) – A coupled model of stomatal conductance, photosynthesis and transpiration – Plant Cell Environ. 26: 1097-1116 – https://doi.org/10.1046/j.13653040.2003.01035.x – https://onlinelibrary.wiley.com/doi/10.1046/j.1365-3040.2003.01035.x – (On our blog : https://plantstomata.wordpress.com/2019/02/12/stomatal-conductance-cannot-be-modelled-in-isolation-but-must-be-fully-coupled-with-models-of-photosynthesis-respiration/ )

Twalla J. T., Ding B., Cao G., Bao S., Li M., Chen X., Xie X., Wang J. (2021) Roles of stomata in gramineous crops growth and biomass production – CEREAL RESEARCH COMMUNICATIONS (2021) – https://doi.org/10.1007/s42976-021-00216-3https://link.springer.com/article/10.1007%2Fs42976-021-00216-3 – (On our blog : https://plantstomata.wordpress.com/2021/12/02/while-stomata-enforce-majority-of-the-essential-processes-in-crops-their-performance-remains-highly-prone-to-the-effects-of-unfavorable-environmental-conditions/ )

Tyree M. T. Nardini A., Salleo S., Sack L., El Omari B. (2005) – The dependence of leaf hydraulic conductance on irradiance during HPFM measurements: any role for stomatal response? – Journ. Exp. Bot. 56: 737-744 – doi:10.1093/jxb/eri045https://sites.lifesci.ucla.edu/eeb-sacklab/wp-content/uploads/sites/71/2016/03/TyreeetalJXB2005.pdf – (On our blog : https://plantstomata.wordpress.com/2019/03/28/the-irradiance-dependence-of-kl-is-more-consistent-with-an-effect-on-extravascular-and-or-vascular-tissues-rather-than-stomatal-aperture/ )

Tyree M. T., Yianoulis P. (1980) – The site of water evaporation from sub-stomatal cavities, liquid path resistance and hydroactive stomatal closure – Annals of Botany 46: 175–193 – https://doi.org/10.1093/oxfordjournals.aob.a085906 –https://academic.oup.com/aob/article-abstract/46/2/175/155121?redirectedFrom=fulltex – (On our blog : https://plantstomata.wordpress.com/2019/02/13/hydroactive-stomatal-closure/ )

Tyutereva E. , Dmitrieva V. , Shavarda A., Voitsekhovskaja O. (2017) – Stomata control is changed in chlorophyll b-free barley mutant – Functional Plant Biology – http://www.publish.csiro.au/FP/justaccepted/FP17056 – (On our blog : https://plantstomata.wordpress.com/2017/10/29/the-chlorophyll-b-free-barley-mutant-and-its-stomata/)

Uddling J., Hall,M., Wallin G., Karlsson P. E. (2005) – Measuring and modelling stomatal conductance and photosynthesis in mature birch in Sweden – Agricultural and Forest Meteorology 132: 115–131 – https://doi.org/10.1016/j.agrformet.2005.07.004 – https://www.sciencedirect.com/science/article/pii/S016819230500136X – (On our blog : https://plantstomata.wordpress.com/2019/02/15/two-multiplicative-models-are-more-successful-in-predicting-stomatal-conductance-than-the-combined-stomatal-photosynthesis-model/ )

Uddling J., Hogg A. J., Teclaw R. M., Mary Anne Carroll M. A., Ellsworth D. S. (2010)  Stomatal uptake of O3 in aspen and aspen-birch forests under free-air CO2 and O3 enrichment – Environmental Pollution 158: 2023–2031 –Stomatal_uptake_of_O3_in_aspen_and_aspen.pdf – (On our blog : https://plantstomata.wordpress.com/2017/12/12/stomatal-uptake-of-o3/ )

Uddling J., Pleijel H. (2006) – Changes in stomatal conductance and net photosynthesis during phonological development in spring wheat: Implications for gas exchange modelling – International Journal of Biometeorology 51: 37–48 – DOI: 10.1007/s00484-006-0039-6 – https://www.ncbi.nlm.nih.gov/pubmed/16733690 – (On our blog : https://plantstomata.wordpress.com/2019/02/15/changes-in-stomatal-conductance-and-net-photosynthesis/ )

Udegbunam S. (2020) – Transpiration in Plants – The Best Learning Guide (2021) – Afrilcate – https://afrilcate.com/transpiration/ – (On our blog : https://plantstomata.wordpress.com/2022/03/29/plant-transpiration/ )

Ueda A., Aihara Y., Sato S., Kano K., Mishiro-Sato E., Kitano H., Sato A., Fujimoto K. J., Yanai T., Amaike K., Kinoshita T., Itami K. (2022) – Discovery of 2,6-Dihalopurines as Stomata Opening Inhibitors: Implication of an LRX-mediated H+-ATPase Phosphorylation Pathway – https://chemrxiv.org/engage/api-gateway/chemrxiv/assets/orp/resource/item/6333edeb084700950b8c2885/original/discovery-of-2-6-dihalopurines-as-stomata-opening-inhibitors-implication-of-an-lrx-mediated-h-at-pase-phosphorylation-pathway.pdf – (On our blog : https://plantstomata.wordpress.com/2023/01/19/26-dihalopurines-as-stomata-opening-inhibitors-and-their-mechanistic-study/ )

Ueno K., Kinoshita T., Inoue S., Emi T., Shimazaki K. (2005) – Biochemical characterization of plasma membrane H+-ATPase activation in guard cell protoplasts of Arabidopsis thaliana in response to blue light – Plant Cell Physiol. 46: 955–963 – doi: 10.1093/pcp/pci104 – https://www.ncbi.nlm.nih.gov/pubmed/15821287 – (On our blog : https://plantstomata.wordpress.com/2018/07/07/arabidopsis-guard-cell-protoplasts-can-be-useful-for-biochemical-analysis-of-stomatal-functions/ )

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