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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 22 (1999), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: 
 A, carbon assimilation rate
ABA, abscisic acid
Ci, intercellular space CO2 concentration
g, leaf conductance
WUE, water use efficiency

Carbon dioxide and abscisic acid (ABA) are two major signals triggering stomatal closure. Their putative interaction in stomatal regulation was investigated in well-watered air-grown or double CO2-grown Arabidopsis thaliana plants, using gas exchange and epidermal strip experiments. With plants grown in normal air, a doubling of the CO2 concentration resulted in a rapid and transient drop in leaf conductance followed by recovery to the pre-treatment level after about two photoperiods. Despite the fact that plants placed in air or in double CO2 for 2 d exhibited similar levels of leaf conductance, their stomatal responses to an osmotic stress (0·16–0·24 MPa) were different. The decrease in leaf conductance in response to the osmotic stress was strongly enhanced at elevated CO2. Similarly, the drop in leaf conductance triggered by 1 μM ABA applied at the root level was stronger at double CO2. Identical experiments were performed with plants fully grown at double CO2. Levels of leaf conductance and carbon assimilation rate measured at double CO2 were similar for air-grown and elevated CO2-grown plants. An enhanced response to ABA was still observed at high CO2 in pre-conditioned plants. It is concluded that: (i) in the absence of stress, elevated CO2 slightly affects leaf conductance in A. thaliana; (ii) there is a strong interaction in stomatal responses to CO2 and ABA which is not modified by growth at elevated CO2.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Stomatal responses to light of Arabidopsis thaliana wild-type plants and mutant plants deficient in starch (phosphoglucomutase deficient) were compared in gas exchange experiments. Stomatal density, size and ultrastructure were identical for the two phenotypes, but no starch was observed in guard cells of the mutant plants whatever the time of day. The overall extent of changes in stomatal conductance during 14 h light–10 h dark cycles was similar for the two phenotypes. However, the slow endogenous stomatal opening occurring in darkness in the wild type was not observed in the mutant plants. Stomata in the mutant plants responded much more slowly to blue light (70 μmol m−2 s−1) though the response to red light (250 μmol m−2 s−1) was similar to that of wild-type plants. In paradermal sections, stomatal responses to red light (300 μmol m−2 s−1) were weak for wild-type plants as well as for mutant plants. Stomatal opening was greater under low blue light (75 μmol m−2 s−1) than under red light for the two genotypes. However, in mutant plants, a high chloride concentration (50 mol m−3) was necessary to achieve the same stomatal aperture as observed for the wild-type plants. These results suggest that starch metabolism, via the synthesis of a counter-ion to potassium (probably malate), is required for full stomatal response to blue light but is not involved in the stomatal response to red light.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Plant, cell & environment 13 (1990), S. 0 
    ISSN: 1365-3040
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Abstract In normal air, illumination with a low level of blue or red light (40 μmol m−2 s−1) did not induce stomatal opening in maize plantlets. In CO2-free air, 40 μmol m−2 s−1 of blue or red light promoted an enhancement in stomatal opening. At the same quantum flux, blue light was more efficient than red light and stomatal closure occurred more rapidly with a significantly shorter lag phase after blue light. Anoxia inhibited light-dependent stomatal opening, even under 320 μmol m−2 s−1 illumination. However, after 60 min of illumination with 40 μmol m−2 s−1 of blue light in anoxia, transient stomatal opening was observed when the plant was returned to darkness and normal air. This transient stomatal opening was weaker after pretreatment with red light. We conclude that a blue-light-dependent process induced under anoxia leads to stomatal opening provided oxygen is present. Possible mechanisms associated with blue-light-effect and the nature of the oxygen-consuming processes are discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 69 (1987), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Maize plants (Zea mays L. hybrid INRA 508) were placed under controlled conditions of light and CO2 partial pressure. The K+, Cl− and P contents were then determined by X-ray microanalysis in the bulbous end of guard cells and in the center of subsidiary cells. The results were interpreted in connection with the stomatal conductance at the time of sampling.In normal air, the K+ and Cl− contents in guard cells only rose from a light threshold of about 300 μmol m−2 s−1 at which stomata were already largely open. At 600 μmol m−2 s−1, the K+ and Cl− levels in guard cells attained values that were 3- and 8-fold greater, respectively, than the values observed in darkness. The K+ and Cl− contents in the subsidiary cells remained quite constant irrespective of the light conditions. CO2-free air in darkness induced a significant K+ influx towards guard and subsidiary cells. Under light and in CO2-free air, the K+ and Cl− contents dramatically increased in the guard cells, but slightly decreased in the subsidiary cells. Thus, when subjected to strong light in CO2-free air, the K+ and Cl− contents in the subsidiary cells were approximately equal to those measured in normal air conditions. In the guard cells, stomatal opening was associated with a marked shift of the Cl−/K+ ratio – from 0.3 for closed stomata to ca 1 for fully open stomata. This could imply a slow change in the nature of the principal counterion accompanying K+ during stomatal opening. The content of P in guard cells appeared, in contrast to that of K+ and Cl−, to be practically independent of stomatal aperture.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Physiologia plantarum 71 (1987), S. 0 
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: In Zea mays L., Bryophylum laxiflorum Bak., Gossypium hirsutum L., Helianthus annuus L., Oryza sativa L. and Vigna radiata L., a pre-illumination in nitrogen causes transient stomatal opening upon returning the plant to darkness and normal air. In Zea mays L. hybrid INRA 508, K+ and Cl− fluctuations in the stomatal complex during this stomatal opening in darkness were similar to those observed during a light-induced opening in normal air. These results are consistent with a two-phase mechanism for stomatal opening: a light phase that may occur in the absence of oxygen and carbon dioxide, and a dark phase during which oxygen is necessary for ion accumulation and other mechanisms of osmotic adjustment.
    Type of Medium: Electronic Resource
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