Access the full text.
Sign up today, get DeepDyve free for 14 days.
C. Black, G. Squire (1979)
Effects of Atmospheric Saturation Deficit on the Stomatal Conductance of Pearl Millet (Pennisetum typhoides S. and H.) and Groundnut (Arachis hypogaea L.)Journal of Experimental Botany, 30
O. Osonubi, W. Davies (1980)
The influence of plant water stress on stomatal control of gas exchange at different levels of atmospheric humidityOecologia, 46
R. Losch (1981)
Stomatal responses to humidity-phenomenon and mechanism
U. Maier-Maercker (1981)
«Peristomatal Transpiration» and Stomatal Movement: A Controversial View: V. Rubidium-86 in the Epidermal Transpiration StreamZeitschrift für Pflanzenphysiologie, 101
H. Meidner (1975)
Water supply, evaporation, and vapour diffusion in leavesJournal of Experimental Botany, 26
H. Meidner, M. Edwards (1975)
Direct Measurements of Turgor Pressure Potentials of Guard Cells, I.Journal of Experimental Botany, 26
U. Maier-Maercker (1979)
«Peristomatal Transpiration» and Stomatal Movement: A Controversial View III. Visible Effects of Peri stomatal Transpiration on the EpidermisZeitschrift für Pflanzenphysiologie, 91
E. Reynolds (1963)
THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPYThe Journal of Cell Biology, 17
A. Spurr (1969)
A low-viscosity epoxy resin embedding medium for electron microscopy.Journal of ultrastructure research, 26 1
Z. Glinka (1971)
The Effect of Epidermal Cell Water Potential on Stomatal Response to Illumination of Leaf Discs of Vicia fabaPhysiologia Plantarum, 24
J. Smith, S. Heuer (1981)
Determination of the Volume of Intercellular Spaces in Leaves and Some Values for CAM PlantsAnnals of Botany, 48
Uta Maercker (1965)
Zur Kenntnis der Transpiration der SchließzellenProtoplasma, 60
C. Osmond, M. Ludlow, R. Davis, I. Cowan, S. Powles, K. Winter (1979)
Stomatal responses to humidity in Opuntia inermis in relation to control of CO2 and H2O exchange patternsOecologia, 41
U. Maier-Maercker (1979)
«Peristomatal Transpiration» and Stomatal Movement: A controversial ViewZeitschrift für Pflanzenphysiologie, 91
E. Schulze, M. Küppers (2004)
Short-term and long-term effects of plant water deficits on stomatal response to humidity in Corylus avellana L.Planta, 146
J. Landsberg, D. Butler (1980)
Stomatal response to humidity: implications for transpirationPlant Cell and Environment, 3
D. Sheriff (1977)
The Effect of Humidity on Water Uptake by, and Viscous Flow Resistance of, Excised Leaves of a Number of Species: Physiological and Anatomical ObservationsJournal of Experimental Botany, 28
E. Schulze, O. Lange, M. Evenari, L. Kappen, U. Buschbom (1975)
The role of air humidity and temperature in controlling stomatal resistance of Prunus armeniaca L. under desert conditionsOecologia, 19
M. Edwards, H. Meidner (1978)
Stomatal Responses to Humidity and the Water Potentials of Epidermal and Mesophyll TissueJournal of Experimental Botany, 29
U. Maercker (1965)
[Contributions to the histochemistry of guard cells].Protoplasma, 60 2
G. Farquhar (1978)
Feedforward Responses of Stomata to HumidityFunctional Plant Biology, 5
P. Jarvis (1964)
THE ADAPTABILITY TO LIGHT INTENSITY OF SEEDLINGS OF QUERCUS PETRAEA (MATT.) LIEBL.Journal of Ecology, 52
E. Ernest (1934)
The Effect of Intercellular Pressure on the Suction Pressure of CellsAnnals of Botany
U. Maier-Maercker (1979)
«Peristomatal Transpiration» and Stomatal Movement: A Controversial View: II. Observation of Stomatal Movements under Different Conditions of Water Supply and DemandZeitschrift für Pflanzenphysiologie, 91
G. Fogg (1966)
The state and movement of water in living organisms.Journal of the Marine Biological Association of the United Kingdom, 46
H. Meidner (1965)
Stomatal control of transpirational water loss.Symposia of the Society for Experimental Biology, 19
E. Schulze, O. Lange, U. Buschbom, L. Kappen, M. Evenari (1972)
Stomatal responses to changes in humidity in plants growing in the desertPlanta, 108
M. Ludlow, N. Turner, P. Kramer (1980)
Adaptive significance of stomatal responses to water stress.
A. Hall, S. Camacho-B, M. Kaufmann (1975)
Regulation of Water Loss by Citrus LeavesPhysiologia Plantarum, 33
O. Lange, R. Lösch, E. Schulze, L. Kappen (1971)
Responses of stomata to changes in humidityPlanta, 100
U. Maier-Maercker (1979)
«Peristomatal Transpiration» and Stomatal Movement: A Controversial View IV. Ion Accumulation by Peristomatal TranspirationZeitschrift für Pflanzenphysiologie, 91
Douglas Johnson, M. Caldwell (1976)
Water Potential Components, Stomatal Function, and Liquid Phase Water Transport Resistances of Four Arctic and Alpine Species in Relation to Moisture StressPhysiologia Plantarum, 36
H. Saxe (1979)
A STRUCTURAL AND FUNCTIONAL STUDY OF THE COORDINATED REACTIONS OF INDIVIDUAL COMMELINA COMMUNIS L. STOMATA (COMMELINACEAE)American Journal of Botany, 66
U. Maier-Maercker (1980)
≪Peristomatal Transpiration≫ and Stomatal Movement: A Controversial View: VI. Lanthanum Deposits in the Epidermal ApoplastZeitschrift für Pflanzenphysiologie, 100
D. Carr (1976)
Plasmodesmata in Growth and Development
Gas exchange measurements made with single leaves from Wych elm ( Ulmus glabra Huds.), Lombardy poplar ( Populus nigra ‘Italica’ L.) and common oak ( Quercus robur L.) seedlings grown at high irradiance showed significant interspecific differences in the stomatal response to variation in atmospheric humidity. Elm and poplar seedlings showed low conductances at high vapour pressure differences (VPD), while the stomatal conductance of oak was little influenced by an increase in VPD between the leaf and the surrounding air. Mild water stress (leaf water potentials of approximately 0.4 MPa) reduced the sensitivity of stomata of elm to humidity and caused almost complete stomatal closure in poplar. Oak seedlings grown at low irradiance showed enhanced stomatal sensitivity to changes in VPD and comparatively high water use efficiencies. Significant reductions in stomatal conductance and transpiration of elm leaves at high VPD suggest that some water loss must occur directly from the external surfaces of the guard cell complex. At high VPD, this loss may maintain the guard cells in a flaccid condition and therefore the stomatal pore will remain closed, even though the plant may be relatively turgid. Differential staining of guard cell walls in light microscope sections of elm and oak leaves suggested an area of the wall that may be permeable to water and transmission electron micrographs revealed a corresponding cuticle-free area on the inner wall of the guard cells of elm leaves. S.E.M. and T.E.M. pictures and light micrographs form the basis of a hypothesis to explain the modifying influence of mild water stress and leaf structure on the response of elm and oak stomata to humidity.
Oecologia – Springer Journals
Published: Jan 1, 1983
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.