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Bresta P., Nikolopoulos D., Economou G., Vahamidis P., Lyra D., Karamanos A., Karabourniotis G. (2011) – Modification of water entry (xylem vessels) and water exit (stomata) orchestrates long term drought acclimation of wheat leaves – Plant and Soil 347(1-2): 179-193 – DOI: 10.1007/s11104-011-0837-4 – https://www.infona.pl/resource/bwmeta1.element.springer-d529decb-208f-3557-a9c3-072cf8f9cc8a – (On our blog : https://plantstomata.wordpress.com/2017/10/08/modification-of-water-entry-xylem-vessels-and-water-exit-stomata-orchestrates-long-term-drought-acclimation/)
Brewer C. A. (1992) – Responses by stomata on leaves to microenvironmental conditions – In C. A. Goldman (Ed.), Tested Studies for Laboratory Teaching (pp. 67-75) – Proceedings of the 13th Workshop/Conference of the Association for Biology Laboratory Education (ABLE) – 191 pages – pp.68-75 –https://www.researchgate.net/profile/Carol-Brewer-2/publication/267838659_Chapter_3_Responses_by_Stomata_on_Leaves_to_Microenvironmental_Conditions/links/56f5583308ae81582bf2109f/Chapter-3-Responses-by-Stomata-on-Leaves-to-Microenvironmental-Conditions.pdf – (On our blog : https://plantstomata.wordpress.com/2021/03/21/88837/ )
Bright J., Desikan R., Hancock J. T., Weir I. S., Neill S. J. (2006) – ABA-induced NO generation and stomatal closure in Arabidopsis are dependent on H2O2 synthesis. – The Plant Journal 45: 113–122 – PMID:16367958 – http://dx.doi.org/10.1111/j.1365-313X.2005.02615.x – (On our blog : https://plantstomata.wordpress.com/2015/09/08/strong-inter-relationship-between-aba-endogenous-h2o2-and-no-induced-stomatal-closure/)
Brillada C., Jiameng Zheng J., Rovira-Diaz E., Rojas-Pierce M., Kruger F., Askani J. C., Schumacher K. (2018) – Phosphoinositides control the localization of HOPS subunit VPS41, which together with VPS33 mediates vacuole fusion in plants – Proceedings of the National Academy of Sciences – DOI: 10.1073/pnas.1807763115 – https://news.ncsu.edu/2018/08/hops-in-vacuole-fusion/ – (On our blog : https://plantstomata.wordpress.com/2018/08/23/vacuoles-control-the-opening-and-closing-of-stomata/ )
Brindley H. M. (1990) – Fluxes of 86Rb+ in “isolated” guard cells of Vicia faba L. – Planta 181: 432–439 – https://www.jstor.org/stable/23380579?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2017/12/11/fluxes-of-86rb-in-stomata/)
Bringmann M., Bergmann D. C. (2013) – Stomatal Patterning. – Encyclopedia of Life Sciences – DOI:10.1002/9780470015902.a0024691 – http://www.els.net/WileyCDA/ElsArticle/refId-a0020125.html – (On our blog : https://plantstomata.wordpress.com/2017/11/01/stomatal-patterning-3/)
Bringmann M., Bergmann D. C. (2017) – Tissue-wide mechanical forces influence the polarity of stomatal stem cell in Arabidopsis – Curr. Biol. 27(6): 877-883 – http://dx.doi.org/10.1016/j.cub.2017.01.059 – https://www.infona.pl/resource/bwmeta1.element.elsevier-29084113-17b4-344d-95cd-7f91a36e79fb – (On our blog : https://plantstomata.wordpress.com/2017/10/22/mechanical-forces-influence-the-polarity-of-stomatal-stem-cells/)
Brinker M., Engelmann W., Kellmann J. W., Piechulla B. (2001) – Circadian rhythms of leaf and stomatal movements in gymnosperm species – Biol. Rhythm Res. 32(4): 471-478 – https://doi.org/10.1076/brhm.32.4.471.1329 – https://www.tandfonline.com/doi/abs/10.1076/brhm.32.4.471.1329 – (On our blog : https://plantstomata.wordpress.com/2020/11/30/a-circadian-clock-controls-leaf-and-stomatal-movements-in-gymnosperm-species/ )
Broadley M. R., Escobar-Gutierrez A. J., Burns A., Burns I. G. (2001) – Nitrogen-limited growth of lettuce is associated with lower stomatal conductance – New Phytol. 152: 97–106 – https://doi.org/10.1046/j.0028-646x.2001.00240.x – https://www.jstor.org/stable/1353584?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2018/10/01/nitrogen-limited-growth-and-lower-stomatal-conductance/ )
Brock A. K., Willmann R., Kolb D., Grefen L., Lajunen H. M., Bethke G., Lee J., Nürnberger T., Gust A. A. (2010) – The Arabidopsis Mitogen-Activated Protein Kinase Phosphatase PP2C5 Affects Seed Germination, Stomatal Aperture, and Abscisic Acid-Inducible Gene Expression – Plant Physiol. 153: 1098–1111 – doi: 10.1104/pp.110.156109 – (On our blog : https://plantstomata.wordpress.com/2016/05/09/pp2c5-and-stomatal-aperture/)
Brodribb Lab Publications: https://wordpress.com/post/plantstomata.wordpress.com/64256
Brodribb T. J. (1996) – Dynamics of Changing Intercellular CO2 Concentration (ci) during Drought and Determination of Minimum Functional ci – Plant Physiology 111: 179-185 – https://doi.org/10.1104/pp.111.1.179 – http://www.plantphysiol.org/content/111/1/179 – (On our blog : https://plantstomata.wordpress.com/2019/11/28/in-the-absence-of-patchy-stomatal-closure-ci-camin-gives-a-good-representation-of-the-drought-tolerance-of-foliage/ )
Brodribb T. J. (2012) – Passive valves or metabolic mouths? The evolution of stomatal physiology – 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/the-ecological-atmospheric-and-physiological-implications-of-a-stomatal-evolutionary-model/ )
Brodribb T. J., Anfodillo T. (2015) – Transport efficiency through uniformity: Organization of veins and stomata in angiosperm leaves – New Phytologist 209(1) – DOI: 10.1111/nph.13577 – https://www.researchgate.net/publication/280585417_Transport_efficiency_through_uniformity_Organization_of_veins_and_stomata_in_angiosperm_leaves – (On our blog : https://plantstomata.wordpress.com/2018/01/20/organization-of-veins-and-stomata-in-angiosperm-leaves/
Brodribb T. J., Hill R. S. (1997) – Imbricacy and stomatal wax plugs reduce maximum leaf conductance in southern hemisphere conifers. – Australian Journal of Botany 45: 657–668 – (On our blog : https://plantstomata.wordpress.com/2016/05/09/imbricacy-stomatal-wax-plugs-and-leaf-conductance/)
Brodribb T. J., Holbrook N. M. (2003) – Stomatal closure during leaf dehydration, correlation with other leaf physiological traits. – Plant Physiology 132(4): 2166–2173 – DOI: https://doi.org/10.1104/pp.103.023879 – http://www.plantphysiol.org/content/132/4/2166 – (On our blog : https://plantstomata.wordpress.com/2017/12/11/what-triggers-stomatal-closure-during-leaf-desiccation/)
Brodribb T. J., Holbrook N. M. (2004) – Stomatal protection against hydraulic failure: a comparison of coexisting ferns and angiosperms. New Phytologist 162: 663-670 – https://doi.org/10.1111/j.1469-8137.2004.01060.x – https://nph.onlinelibrary.wiley.com/doi/10.1111/j.1469-8137.2004.01060.x – (On our blog : https://plantstomata.wordpress.com/2015/09/08/behaviour-of-stomata-in-pteridophytes-and-angiosperms/).
Brodribb T. J., Holbrook N. M. (2004) – Diurnal depression of leaf hydraulic conductance in a tropical tree species – Plant, Cell and Environment 27: 820-827 – (On our blog : https://plantstomata.wordpress.com/2015/09/08/diurnal-patterns-of-hydraulic-conductance-in-a-tropical-tree-species/).
Brodribb T. J., Holbrook N. M., Edwards E. J., Guttiérrez M. V. (2003) – Relations between stomatal closure, leaf turgor and xylem vulnerability in eight tropical dry forest trees – Plant Cell Environ. 26(3): 443–450 – DOI: 10.1046/j.1365-3040.2003.00975.x – http://onlinelibrary.wiley.com/doi/10.1046/j.1365-3040.2003.00975.x/abstract – (On our blog : https://plantstomata.wordpress.com/2016/05/09/stomatal-closure-leaf-turgor-and-xylem-vulnerability/)
Brodribb T. J., Jordan G.J. (2008) – Internal coordination between hydraulics and stomatal control in leaves – Plant Cell Environ. 31: 1557-1564 – http://dx.doi.org/10.1111/j.1365-3040.2008.01865.x – PMid:18684244 – https://onlinelibrary.wiley.com/doi/full/10.1111/j.1365-3040.2008.01865.x – (On our blog : https://plantstomata.wordpress.com/2015/09/09/stomatal-control-in-leaves-and-hydraulics/).
Brodribb Lab – Stomatal Function and Evolution – http://www.brodribblab.org.au/research-areas/stomatal-function-and-evolution/ – (On our blog : https://plantstomata.wordpress.com/2017/01/03/stomatal-function-and-evolution-at-the-brodribb-lab/)
Brodribb T. J., McAdam S. A. M. (2011) – A Tale of Two Stomata – Science 331(6017): 509 – DOI: 10.1126/science.331.6017.509-a – https://science.sciencemag.org/content/331/6017/509.1 – (On our blog : https://plantstomata.wordpress.com/2020/12/07/stomata-of-seed-bearing-plants-function-differently-than-those-of-spore-bearing-plants/ )
Brodribb T. J., McAdam S. A. M. (2011) – Passive origins of stomatal control in vascular plants – Science 331: 582-585 – doi: 10.1126/science.1197985 – Epub 2010 Dec 16 – PMID: 21163966 – (On our blog : https://plantstomata.wordpress.com/2015/09/09/different-behavior-of-stomata-in-early-vascular-plants-and-seed-plants/)
Brodribb T. J., McAdam S. A. M. (2012) – Fern and lycophyte guard cells do not respond to endogenous ABA – The Plant Cell 24: 1510–1521 – doi: 10.1105/tpc.112.096404 – https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3398560/?report=reader#__ffn_sectitle – (On our blog : https://plantstomata.wordpress.com/2020/03/03/endogenous-aba-synthesized-by-ferns-and-lycophytes-plays-little-role-in-the-regulation-of-transpiration-with-stomata-passively-responsive-to-leaf-water-potential/ )
Brodribb T. J., McAdam S. A. M. (2012) – Stomatal (mis)behaviour – Tree Physiol. 31(10): 1039-1040 – doi: 10.1093/treephys/tpr100 – Epub 2011 Sep 24 – PMID: 21949027 – https://www.ncbi.nlm.nih.gov/pubmed/21949027 – (On our blog : https://plantstomata.wordpress.com/2018/10/01/stomatal-misbehaviour/ )
Brodribb T. J., McAdam S. A. M. (2013) – Abscisic acid mediates a divergence in the drought response of two conifers. – Plant Physiol. 162(3): 1370-1377 – doi: 10.1104/pp.113.217877 – Epub 2013 May 24 – PMID: 23709665 – http://www.brodribblab.org.au/wp-content/uploads/2014/05/ABA-and-drought-response-Plant-Phys-Brodribb-McAdam.pdf – (On our blog : https://plantstomata.wordpress.com/2016/02/19/two-contrasting-mechanisms-of-stomatal-regulation/).
Brodribb T. J., McAdam S. A. M. (2013) – Unique responsiveness of angiosperm stomata to elevated CO2 explained by calcium signalling. – PLoS One 8(11): e82057 – doi: 10.1371/journal.pone.0082057 – eCollection 2013 – PMID: 24278470 – (On our blog : https://plantstomata.wordpress.com/2016/02/19/unique-responsiveness-of-angiosperm-stomata/).
Brodribb T. J., McAdam S. A. M. (2015) – Evolution in the smallest valves (stomata) guides even the biggest trees – Tree Physiol. 35(5): 451-452 – doi: 10.1093/treephys/tpv042 – PMID:-26041093 – https://academic.oup.com/treephys/article/35/5/451/1642114 – (On our blog : https://plantstomata.wordpress.com/2018/10/11/different-ways-sister-species-respond-to-water-stress/ )
Brodribb T. J., McAdam S. A. M. (2017) – Evolution of the stomatal regulation of plant water content – Plant Physiology 174(2): 639-649 – DOI: 10.1104/pp.17.00078 – https://www.researchgate.net/publication/316111982_Evolution_of_the_stomatal_regulation_of_plant_water_content – (On our blog : https://plantstomata.wordpress.com/2017/06/25/the-function-of-early-stomata/)
Brodribb T. J., McAdam S. A. M., Carins Murphy M. R. (2017) – Xylem and Stomata, Coordinated Through Time and Space – Plant Cell and Environment 40: 872-880 – DOI: 10.1111/pce.12817 – https://www.researchgate.net/publication/306271326_Xylem_and_Stomata_Coordinated_Through_Time_and_Space – (On our blog : https://plantstomata.wordpress.com/2016/08/20/evolution-in-xylem-and-stomatal-function-and-their-interaction/)
Brodribb T. J., McAdam S. A. M., Jordan G. J., Feild T. S. (2009) – Evolution of stomatal responsiveness to CO2 and optimization of water-use efficiency among land plants – New Phytol. 183(3): 839-847 – doi: 10.1111/j.1469-8137.2009.02844.x – Epub 2009 Apr 23 – PMID: 19402882 – – (On our blog : https://plantstomata.wordpress.com/2016/05/10/stomatal-responsiveness-to-co2-and-optimization-of-wue/)
Brodribb T. J., McAdam S. A., Jordan G. J., Martins S. C. ( 2014) – Conifer species adapt to low-rainfall climates by following one of two divergent pathways. – Proc Natl Acad Sci U S A. 111(40): 14489-14493 – doi: 10.1073/pnas.1407930111 – Epub 2014 Sep 22 – – https://www.ncbi.nlm.nih.gov/pubmed/25246559 – (On our blog : https://plantstomata.wordpress.com/2016/12/31/the-simple-way-conifers-evolved-to-cope-with-water-shortage-a-critical-interaction-between-xylem-and-stomatal-tissues/)
Brodribb T. J., Sussmilch F., McAdam S. A. M. (2019) – From reproduction to production, stomata are the master regulators – The Plant Journal – Early View – Special Issue Article – https://doi.org/10.1111/tpj.14561 – https://onlinelibrary.wiley.com/doi/abs/10.1111/tpj.14561 – (On our blog : https://plantstomata.wordpress.com/2019/11/21/stomata-are-the-master-regulators/)
Brogårdh T., Johnsson A. (1974) – Effects of Lithium on Stomatal Regulation – Zeitschr. Naturforsch C Biosci 29(5): 298-300 – file:///C:/Users/wille/Downloads/10.1515_znc-1974-5-622%20(1).pdf – (On our blog : https://plantstomata.wordpress.com/2021/10/04/an-action-of-lithium-on-a-much-more-rapid-oscillation-which-under-certain-circumstances-occurs-in-stomatal-regulation/ )
Brogårdh T., Johnsson A. (1975) – Effects of Magnesium, Calcium and Lanthanum Ions on Stomatal Oscillations in Avena sativa L. – Planta 124(1): 99-103 – https://www.jstor.org/stable/23371619 – https://www.jstor.org/stable/23371619?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2019/04/03/effects-of-mg-ca-and-la-ions-on-stomatal-oscillations/ )
Brookbank B. P., Patel J., Gazzarrini S., Nambara E. (2021) – Role of Basal ABA in Plant Growth and Development – Genes 12(12): 1936- 22pp. – https://doi.org/10.3390/genes12121936 – https://www.mdpi.com/2073-4425/12/12/1936 – (On our blog : https://plantstomata.wordpress.com/2022/01/26/aba-and-stomata/ )
Brosché M., Merilo E., Mayer F ., Pechter P., Puzörjova I., Brader G ., Kangasjärvi J., Kollist H. (2010) – Natural variation in ozone sensitivity among Arabidopsis thaliana accessions and its relation to stomatal conductance – Plant Cell Environ. 33: 914-925 – DOI: 10.1111/j.1365-3040.2010.02116.x – http://onlinelibrary.wiley.com/doi/10.1111/j.1365-3040.2010.02116.x/full – (On our blog : https://plantstomata.wordpress.com/2016/10/10/the-role-of-stomata-in-regulating-o3-entry-and-damage/)
Brown A. B. (1931) – Effects of temperature on stomata ofexcised leaves of Zebrina pendula – https://escholarship.mcgill.ca/concern/theses/8g84mq42k – https://escholarship.mcgill.ca/concern/theses/8g84mq42k?locale=en –
Brown K. W., Jordan W. R., Thomas J. C. (1976) – Water stress induced alterations of the stomatal response to decreases in leaf water potential – Physiologia Plantarum 37: 1-5 – https://doi.org/10.1111/j.1399-3054.1976.tb01863.x – https://onlinelibrary.wiley.com/doi/10.1111/j.1399-3054.1976.tb01863.x – (On our blog : https://plantstomata.wordpress.com/2019/12/10/water-stress-induced-alterations-of-the-stomatal-response-to-decreases-in-leaf-water-potential/ )
Brown K. W., Rosenberg N. J. (1970) – Effect of Windbreaks and Soil Water Potential on Stomatal Diffusion Resistance and Photosynthetic Rate of Sugar Beets (Beta vulgaris) – Agronomy Journal 62(1): 4-8 – https://doi.org/10.2134/agronj1970.00021962006200010002x – https://acsess.onlinelibrary.wiley.com/doi/abs/10.2134/agronj1970.00021962006200010002x – (On our blog : https://plantstomata.wordpress.com/2021/12/07/effect-of-windbreaks-and-soil-water-potential-on-stomatal-diffusion-resistance/ )
Brown K. W., Rosenberg N. J. (1970) – Influence of leaf age, illumination, and upper and lower surfaces on stomatal resistance of sugar beet (Beta vulgaris) leaves – Agron. J. 62: 20-24 – doi:10.2134/agronj1970.00021962006200010007x – https://dl.sciencesocieties.org/publications/aj/abstracts/62/1/AJ0620010020?access=0&view=pdf – (On our blog : https://plantstomata.wordpress.com/2018/04/12/influence-of-leaf-age-illumination-and-upper-and-lower-surfaces-on-stomatal-resistance/ )
Brown P. H., Outlaw W. H. (1982) – Effect of Fusicoccin on Dark 14CO2 Fixation by Vicia faba Guard Cell Protoplasts – Plant Physiol. 70(6): 1700–1703 – DOI: https://doi.org/10.1104/pp.70.6.1700 – – http://www.plantphysiol.org/content/plantphysiol/70/6/1700.full.pdf – (On our blog : https://plantstomata.wordpress.com/2018/04/12/effect-of-fusicoccin-on-dark-14co2-fixation-by-stomatal-protoplasts/ )
Brown W. V., Johnson S. C. (1962) – The fine structure of the grass guard cell – Am. J. Bot. 49: 110-115 – https://www.jstor.org/stable/2439025?seq=1#page_scan_tab_contents – (On our blog : https://plantstomata.wordpress.com/2017/11/13/structure-of-grass-stomata/)
Brown W. V., Pratt G. A. (1965) – Stomatal Inactivity in Grasses – The Southwestern Naturalist 10(1): 48-56 – https://www.jstor.org/stable/3669389 – (On our blog : https://plantstomata.wordpress.com/2021/12/11/differences-in-stomatal-opening-in-grasses/ )
Brownlee C. (2001) – The long and the short of stomatal density signals. -Trends Plant Sci 6:441-442. – DOI: http://dx.doi.org/10.1016/S1360-1385(01)02095-7 – http://www.esalq.usp.br/lepse/imgs/conteudo_thumb/The-long-and-the-short-of-stomatal-density-signals.pdf – (On our blog : https://plantstomata.wordpress.com/2015/09/09/the-density-and-patterning-of-stomata-in-response-to-environmental-stimuli/)
Brownlee C. (2018) – Stomatal Physiology: Cereal Successes – Current Biology 28(9): R551-R553 – https://doi.org/10.1016/j.cub.2018.03.055 – https://www.sciencedirect.com/science/article/pii/S0960982218304135 – (On our blog : https://plantstomata.wordpress.com/2020/09/06/stomatal-physiology-cereal-successes/ )
Brüggemann L., Dietrich P., Becker D., Dreyer I., Palme K., Hedrich R. (1999) – Channel‐mediated high‐affinity K+ uptake into guard cells from Arabidopsis – Proceedings of the National Academy of Sciences USA 96: 3298-3302 -PMID: 10077678 PMCID: PMC15936 – https://www.ncbi.nlm.nih.gov/pubmed/10077678 – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/71187 )
Brüggemann L., Dietrich P., Dreyer I., Hedrich R. (1999) – Pronounced differences between the native K+ channels and KAT1 and KST1 alpha‐subunit homomers of guard cells – Planta 207: 370-376 – PMID: 9951733 – https://www.ncbi.nlm.nih.gov/pubmed/9951733 – (On our blog : https://plantstomata.wordpress.com/2018/09/12/differences-between-the-native-k-channels-and-kat1-and-kst1-alpha%e2%80%90subunit-homomers-of-stomata/ )
Brugnoli E., Björkman O. (1992) – Growth of cotton under continuous salinity stress: Influence on allocation pattern, stomatal and non-stomatal components of photosynthesis and dissipation of excess light energy – Planta 187: 335-347 – https://doi.org/10.1007/BF00195657 – https://link.springer.com/article/10.1007/BF00195657#citeas – (On our blog : https://plantstomata.wordpress.com/2019/04/18/influence-of-salinity-stress-on-stomatal-and-non-stomatal-components-of-photosynthesis/ )
Brugnoli E., Lauteri M. (1991) – Effects of Salinity on Stomatal Conductance, Photosynthetic Capacity, and Carbon Isotope Discrimination of Salt-Tolerant (Gossypium hirsutum L.) and Salt-Sensitive (Phaseolus vulgaris L.) C3 Non-Halophytes – Plant Physiology 95(2): 628-635 – https://doi.org/10.1104/pp.95.2.628 – http://www.plantphysiol.org/content/plantphysiol/95/2/628.full.pdf – (On our blog : https://plantstomata.wordpress.com/2017/09/30/effects-of-salinity-on-growth-and-stomatal-conductance/)
Brun W. A. (1962) – Rhythmic stomatal opening responses in banana leaves – Physiol. Plant. 15: 623-630 – DOI: 10.1111/j.1399-3054.1962.tb08110.x – http://onlinelibrary.wiley.com/doi/10.1111/j.1399-3054.1962.tb08110.x/full – (On our blog : https://plantstomata.wordpress.com/2018/02/19/rhythmic-stomatal-opening-responses/ )
Bruns H. N. (2016) – Flag Leaf Photosynthesis and Stomatal Function of Grain Sorghum as Influenced by Changing Photosynthetic Photon Flux Densities – International Journal of Agronomy 2016, Article ID 1363740, 6 pp. – http://dx.doi.org/10.1155/2016/1363740 – https://www.hindawi.com/journals/ija/2016/1363740/ – (On our blog : https://plantstomata.wordpress.com/2017/11/27/stomatal-function-of-grain-sorghum/)
Bucher S. F., Auerswald K., Grün-Wenzel C., Higgins S. I., Garcia Jorge J., Römermann C. (2017) – Stomatal traits relate to habitat preferences of herbaceous species in a temperate climate – Flora 229: 107-115 – DOI: 10.1016/j.flora.2017.02.011 – https://www.infona.pl/resource/bwmeta1.element.elsevier-d3f42e76-ec23-32b1-9ab2-5bbdb53fa470 – (On our blog : https://plantstomata.wordpress.com/2017/10/09/stomatal-traits-such-as-size-density-or-distribution-as-indicators/)
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Chen D., Cao Y., Li H., Kim D., Ahsan N., Thelen J., Stacey G. (2017) – Extracellular ATP elicits DORN1-mediated RBOHD phosphorylation to regulate stomatal aperture – Nature Communications 8, Article number: 2265 – doi:10.1038/s41467-017-02340-3 – https://www.nature.com/articles/s41467-017-02340-3 – (On our blog : https://plantstomata.wordpress.com/2018/01/02/dorn1-regulates-stomatal-closure-and-bacterial-defense/)
Chen D.-H., Acharya B., Liu W., Zhang W. (2013) – Interaction between Calcium and Actin in Guard Cell and Pollen Signaling Networks – Plants 2(4): 615 – doi:10.3390/plants2040615 – http://www.mdpi.com/2223-7747/2/4/615/pdf – (On our blog : https://plantstomata.wordpress.com/2017/11/13/calcium-and-actin-in-stomata/)
Chen D.-H., Liu H. P., Li C. L. (2019) – Calcium-dependent protein kinase CPK9 negatively functions in stomatal abscisic acid signaling by regulating ion channel activity in Arabidopsis – Plant Mol Biol. 99(1-2): 113-122 – doi: 10.1007/s11103-018-0805-y – Epub 2018 Dec 8 – https://www.ncbi.nlm.nih.gov/pubmed/30536042 – (On our blog : https://plantstomata.wordpress.com/2019/09/08/the-role-of-cpk9-in-stomatal-guard-cells-and-the-need-of-both-cpk9-and-cpk33-for-accurate-guard-cell-function/ )
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Chen G., Wang Y., Wang X., Yang Q., Quan X., Zeng J., Dai F., Zeng F., Wu F., Zhang G. (2018) – Leaf epidermis transcriptome reveals drought-Induced hormonal signalling for stomatal regulation in wild barley – Plant Growth Regulation 87: 39-54 – https://doi.org/10.1007/s10725-018-0450-0 – https://link.springer.com/article/10.1007/s10725-018-0450-0#citeas – (On our blog : https://plantstomata.wordpress.com/2022/12/08/drought-induced-hormonal-signalling-for-stomatal-regulation-in-wild-barley/ )
Chen H., Zhao X., Zhai L., Shao K., Jiang K., Shen C., Chen K., Wang S., Wang Y., Xu J. (2020) – Genetic Bases of the Stomata-Related Traits Revealed by a Genome-Wide Association Analysis in Rice (Oryza sativa L.) – Frontiers in Genetics 11
Chen J. W., Zhang Q., Li X. S., Cao K. F. (2010) – Gas exchange and hydraulics in seedlings of Hevea brasiliensis during water stress and recovery – Tree Physiol. 30(7): 876-885 – doi: 10.1093/treephys/tpq043 – Epub 2010 Jun 1 – PMID: 20516484 – https://pubmed.ncbi.nlm.nih.gov/20516484/ – (On our blog : https://plantstomata.wordpress.com/2022/08/26/stomatal-closure-effectively-reduces-the-risk-of-xylem-dysfunction-in-water-stressed-plants-at-the-cost-of-gas-exchange/ )
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Chen L., Cochran A. M., Waite J. M., Shirasu K., Bemis S. M., Torii K. U. (2022) – Direct attenuation of Arabidopsis ERECTA signalling by a pair of U-box E3 ligases – Nat. Plants – https://doi.org/10.1038/s41477-022-01303-x – https://www.nature.com/articles/s41477-022-01303-x#citeas – (On our blog : https://plantstomata.wordpress.com/2023/01/12/pub30-and-pub31-as-key-attenuators-of-erecta-signalling-for-two-developmental-processes-inflorescence-pedicel-growth-and-stomatal-development/)
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Chen L., Guan L., Qian P., Xu F., Wu Z., Wu Y., He K., Gou X., Li J., Hou S. (2016) – NRPB3, the third largest subunit of RNA polymerase II, is essential for stomatal patterning and differentiation in Arabidopsis – Development 143: 1600–1611 – doi: 10.1242/dev.129098 – https://dev.biologists.org/content/143/9/1600 – (On our blog : https://plantstomata.wordpress.com/2020/05/03/nrpb3-serves-as-an-acceptor-for-signals-from-transcription-factors-involved-in-stomatal-development/ )
Chen L., Wu Z., Hou S. (2020) – SPEECHLESS Speaks Loudly in Stomatal Development – Front. Plant Sci., 21 February 2020 – https://doi.org/10.3389/fpls.2020.00114 – https://www.frontiersin.org/articles/10.3389/fpls.2020.00114/full – (On our blog : https://plantstomata.wordpress.com/2020/05/03/reinforcing-the-idea-that-spch-is-the-central-molecular-hub-for-stomatal-development/ )
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Chen L. Q., Li C. S., Chaloner W. G., Beerling D. J., Sun Q. G., Collinson M. E., Mitchell P. L. (2001) – Assessing the potential for the stomatal characters of extant and fossil Ginkgo leaves to signal atmospheric CO2 change – Am J Bot. 88: 1309–1315 – PMID: 11454631 – https://www.ncbi.nlm.nih.gov/pubmed/11454631 – (On our blog : https://plantstomata.wordpress.com/2019/09/05/the-potential-for-the-stomatal-characters-of-extant-and-fossil-ginkgo-leaves-to-signal-atmospheric-co2-change/ )
Chen P.-Y., Ma M., Shi L.-y. (2019) – Trade-off Between Salt Secretion and Gas Exchange by Stomata in the Leaves of Glycyrrhiza uralensis – CURRENT SCIENCE 116(7): 1212-1217 – https://www.currentscience.ac.in/Volumes/116/07/1212.pdf – https://www.currentscience.ac.in/php/forthcoming/2019/31209.pdf – (On our blog : https://plantstomata.wordpress.com/2019/03/25/stomata-of-the-upper-leaves-are-mainly-used-for-gas-exchange-stomata-of-the-lower-leaves-are-responsible-for-secreting-excessive-salt/)
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Chen S., Assmann S. (2018) – Deciphering the guard cell metabolome in plant pathogen defense – https://fsrio.nal.usda.gov/fsrio/research-projects/deciphering-guard-cell-metabolome-plant-pathogen-defense – (On our blog : https://plantstomata.wordpress.com/2018/10/08/deciphering-the-stomatal-metabolome-in-plant-pathogen-defense/ )
Chen S., Jia H., Wang X., Shi C., Wang X., Ma P., Wang J., Ren M., Li J. (2020) – Hydrogen sulfide positively regulates abscisic acid signaling through persulfidation of SnRK2.6 in guard cells – Mol. Plant. 13: 732–744 – doi: 10.1016/j.molp.2020.01.004 – https://pubmed.ncbi.nlm.nih.gov/31958520/ – (On our blog : https://plantstomata.wordpress.com/2021/07/08/a-novel-post-translational-regulatory-mechanism-of-aba-signaling-whereby-h2s-persulfidates-snrk2-6-to-promote-aba-signaling-and-aba-induced-stomatal-closure/ )
Chen S.-N., Chen Z.-S.-N., Zhang Z.-Q. (2021) – Canopy stomatal conductance characteristics of Pinus tabulaeformis and Acer truncatum and their responses to environmental factors in the mountain area of Beijing – Chin J Plant Ecol 45(12): 1329-1340 – DOI: 10.17521/cjpe.2021.0198 – https://www.plant-ecology.com/EN/10.17521/cjpe.2021.0198 – (On our blog : https://plantstomata.wordpress.com/2023/02/05/the-response-of-stomata-to-environmental-factors-differs-between-tree-species-and-different-periods-of-the-growing-season/ )
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Chen W. F., Xu Z. J., Zhang L. B., Yang S. R. (1990) – Comparative studies on stomatal density and its relations to gas diffusion resistance and net photosynthetic rate in rice leaf – Chin J Rice Sci 4: 163–168 – https://www.cabdirect.org/cabdirect/abstract/19910744617 – (On our blog : https://plantstomata.wordpress.com/2020/03/10/comparative-studies-on-stomatal-density-and-its-relations-to-gas-diffusion-resistance/ )
Chen W.-L., Yang W.-J., Lo H.-F., Yeh D.-M. (2014) – Physiology, anatomy, and cell membrane thermostability selection of leafy radish (Raphanus sativus var. oleiformis Pers.) with different tolerance under heat stress – Scientia Horticutlturae 179: 364-375 – https://doi.org/10.1016/j.scienta.2014.10.003 –https://www.sciencedirect.com/science/article/pii/S0304423814005524 – (On our blog : https://plantstomata.wordpress.com/2019/04/11/line-9911-9-of-leafy-radish-was-able-to-tolerant-high-temperature-through-diminishing-both-stomatal-and-non-stomatal-limitations/ )
Chen W. Y., Liu C. H., Li Y. Y., Mi D. H. (2014) – Flag leaf vein traits in winter wheat varieties (lines) and their correlation with stomatal traits – Chin J Ecol. 33(7): 1839–1846 –
Chen Y., Li W., Turner J. A., Anderson C. T. (2021) – PECTATE LYASE LIKE12 patterns the guard cell wall to coordinate turgor pressure and wall mechanics for proper stomatal function in Arabidopsis – The Plant Cell https://doi.org/10.1093/plcell/koab161 – https://pubmed.ncbi.nlm.nih.gov/34109391/ – (On our blog : https://plantstomata.wordpress.com/2021/07/21/how-wall-modifying-genes-modulate-wall-mechanics-and-cell-pressurization-to-accomplish-the-dynamic-cellular-deformations-that-underlie-stomatal-function/ )
Chen Y., Zhu W., Yan T., Chen D., Jiang L., Chen Z. H., Wu D. (2022) – Stomatal morphological variation contributes to global ecological adaptation and diversification of Brassica napus – Planta 256(4): 64 – doi: 10.1007/s00425-022-03982-4 – PMID: 36029339 – https://pubmed.ncbi.nlm.nih.gov/36029339/ – (On our blog : https://plantstomata.wordpress.com/2022/09/02/the-relation-between-stomatal-phenotypic-variation-and-ecological-adaptation-in-rapeseed/ )
Chen Y.-H., Hu L., Punta M., Bruni R., Hillerich B., Kloss B., Rost B., Love J., Siegelbaum S. A., Hendrickson W. A. (2010) – Homologue structure of the SLAC1 anion channel for closing stomata in leaves – Nature 467: 1074–1080 – doi:10.1038/nature09487 – http://www.nature.com/nature/journal/v467/n7319/full/nature09487.html – (On our blog : https://plantstomata.wordpress.com/2017/09/17/a-bacterial-homologue-of-slac1-for-closing-stomata/)
Chen Y.-L., Huang R., Xiao Y.-M., Lü P., Chen J., Wang X.-C. (2004) – Extracellular Calmodulin-Induced Stomatal Closure Is Mediated by Heterotrimeric G Protein and H2O2 – Plant Physiology 136: 4096–4103 – Extracellular_Calmodulin-Induced_Stomata.pdf – (On our blog : https://wordpress.com/post/plantstomata.wordpress.com/64726)
Chen Y.-L., Zhang X. Q., Chen J., Wang X.-C. (2003) – Existence of extracellular CaM in abaxial epidermis of Vicia faba L. and its role in regulation of stomatal movements – Acta Bot Sin 45:40–46 – https://europepmc.org/abstract/cba/361042 – (On our blog : https://plantstomata.wordpress.com/2018/09/05/endogenous-extracellular-cam-promotes-stomatal-closure-and-inhibits-stomatal-opening/ )
Chen Z., Gallie D. R. (2004) – The ascorbic acid redox state controls guard cell signaling and stomatal movement. – Plant Cell. 2004;166(1):1143–1162. [PMC free article] [PubMed] – (On our blog : https://plantstomata.wordpress.com/2016/07/16/the-asc-redox-state-and-stomatal-movements/)
Chen Z., Li S., Luan J., Zhang Y., Zhu S., Wan X., Liu S. (2019) – Prediction of temperate broadleaf tree species mortality in arid limestone habitats with stomatal safety margins – Tree Physiol. 39(8): 1428-1437 – doi: 10.1093/treephys/tpz045 – PMID: 30977822 – https://pubmed.ncbi.nlm.nih.gov/30977822/ – (On our blog : https://plantstomata.wordpress.com/2022/12/02/the-stomatal-safety-margin-as-the-indicator-for-predicting-drought-induced-tree-mortality/ )
Chen Z., Li S., Wan X., Liu S. (2022) – Strategies of tree species to adapt to drought from leaf stomatal regulation and stem embolism resistance to root properties – Front Plant Sci 13: 926535 – doi: 10.3389/fpls.2022.926535 – eCollection 2022 – PMID: 36237513 – PMCID: PMC9552884 – https://pubmed.ncbi.nlm.nih.gov/36237513/ – (On our blog : https://plantstomata.wordpress.com/2022/12/02/adaptation-to-drought-from-leaf-stomatal-regulation-and-stem-embolism-resistance-to-root-properties/ )
Chen Z., Liu S., Lu H., Wan X. (2019) – Interaction of stomatal behaviour and vulnerability to xylem cavitation determines the drought response of three temperate tree species – AoB PLANTS 11: plz058 – doi: 10.1093/aobpla/plz058 – (On our blog : https://plantstomata.wordpress.com/2022/05/10/hsm-hydraulic-safety-margin-as-well-as-ssm-stomatal-safety-margin-allow-interpreting-the-sensitivity-of-the-three-sub-canopy-species-to-drought/ )
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PLANT STOMATA ENCYCLOPEDIA 