Manuscript submitted to Plant Physiology (Update) 1 2 Running Head: Leaf hydraulics and stomatal conductance 3 4 Corresponding author: 5 Fulton E. Rockwell 6 Harvard University 7 Department of Organismic and Evolutionary Biology 8 Cambridge, MA 02138. 9 Phone: (617) 496-0603 10 Email: [email protected] 11 12 Research Area: 13 Focus Issue on water: Update on stomata, Ecophysiology and Su...

Stomata control the flow of gases between plants and the atmosphere. This review is centered on stomatal responses to elevated CO2 concentration and considers other key environmental factors and underlying mechanisms at multiple levels. First, an outline of general responses in stomatal conductance under elevated CO2 is presented. Second, stomatal density response, its development, and the trad...

The current scenario of global warming has resulted in considerable uncertainty regarding the capacity of forest trees to adapt to increasing drought. Detailed ecophysiological knowledge would provide a basis to forecast expected species dynamics in response to climate change. Here, we compare the water balance (stomatal conductance, xylem water potential, needle osmotic adjustment) of Abies pi...

The physiological and physical components of the feedback loop involving intercellular CO(2) concentration (c(i)) and stomata are identified. The loop gain (G) is a measure of the degree of homeostasis in a negative feedback loop [the expression 1/(1-G) represents the fraction to which feedback reduces a perturbance]. Estimates are given for the effects of G on responses of stomata and c(i) to ...

Uptake of CO(2) by the leaf is associated with loss of water. Control of stomatal aperture by volume changes of guard cell pairs optimizes the efficiency of water use. Under water stress, the protein kinase OPEN STOMATA 1 (OST1) activates the guard-cell anion release channel SLOW ANION CHANNEL-ASSOCIATED 1 (SLAC1), and thereby triggers stomatal closure. Plants with mutated OST1 and SLAC1 are de...

Plant physiological adaptation to the global rise in atmospheric CO(2) concentration (CO(2)) is identified as a crucial climatic forcing. To optimize functioning under rising CO(2), plants reduce the diffusive stomatal conductance of their leaves (g(s)) dynamically by closing stomata and structurally by growing leaves with altered stomatal densities and pore sizes. The structural adaptations re...

Responses of stomata to environment have been intensively studied, but little is known of genetic effects on stomatal conductance or their consequences. In Pima cotton (Gossypium barbadense L.), a crop that is bred for irrigated production in very hot environments, stomatal conductance varies genetically over a wide range and has increased with each release of new higher-yielding cultivars. A c...

The terrestrial hydrological cycle is strongly influenced by transpiration--water loss through the stomatal pores of leaves. In this report we present studies showing that the energy content of radiation absorbed by the leaf influences stomatal control of transpiration. This observation is at odds with current concepts of how stomata sense and control transpiration, and we suggest an alternativ...

Plant gas exchange is a key process shaping global hydrological and carbon cycles and is often characterized by plant water use efficiency (WUE - the ratio of CO2 gain to water vapor loss). Plant fossil record suggests that plant adaptation to changing atmospheric CO2 involved correlated evolution of stomata density (d) and size (s), and related maximal aperture, amax . We interpreted the fossi...