Attempts to correlate values of stomatal conductance and leaf water potential with particular environmental variables in the field are generally of only limited success because they are simultaneously affected by a number of environmental variables. For example, correlations between leaf water potential and either flux of radiant energy or vapour pressure deficit show a diurnal hysteresis which leads to a scatter diagram if many values are plotted. However, a simple model may be adequate to relate leaf water potential to the flow of water through the plant. The stomatal conductance of illuminated leaves is a function of current levels of temperature, vapour pressure deficit, leaf water potential (really turgor pressure) and ambient CO $_2$ concentration. Consequently, when plotted against any one of these variables a scatter diagram results. Physiological knowledge of stomatal functioning is not adequate to provide a mechanistic model linking stomatal conductance to all these variables. None the less, the parameters describing the relationships with the variables can be conveniently estimated from field data by a technique of non-linear least squares, for predictive purposes and to describe variations in response from season to season and plant to plant.

The Interpretation of the Variations in Leaf Water Potential and Stomatal Conductance Found in Canopies in the Field

INTRODUCTION 492 ECOLOGICAL ASPECTS OF PHOTOSYNTHETIC TEMPERATURE ADAPTATION 493 Photosynthetic Temperature Dependence in Thermally Contrasting Climates ........ 493 Photosynthetic Temperature Acclimation 497 Seasonal acclimation in natural habitats ...... ....... 497 Studies in controlled environments 499 THE MECHANISTIC BASIS FOR PHOTOSYNTHETIC RESPONSE AND ADAPTATION TO TEMPERATURE 504 Reversible Temperature Respon.ses 505 Stomata! effec� o� the . temJH!.rature response 0/ photo.rynthesis ......... ....... 505 Interacttons with /lght mtenslty 507 C, photo.rynthesis (lM photorespiration 507 C, photo.rynthesis 515 Comparison 0/ plants from contrasting thermol regimes ...... ...... 517 ["eversible Temperature Respon.ses 519 Low temperature sensitMty ....... 519 High temperature sensitivity 524 Adoptive responses in the heat stability 0/ the photosynthetic apparatus 530 CONCLUDING REMARKS 532

Photosynthetic Response and Adaptation to Temperature in Higher Plants

Characterization and Distribution of Water-repellent, Self-cleaning Plant Surfaces

Stomata, the small pores on the surfaces of leaves and stalks, regulate the flow of gases in and out of leaves and thus plants as a whole. They adapt to local and global changes on all timescales from minutes to millennia. Recent data from diverse fields are establishing their central importance to plant physiology, evolution and global ecology. Stomatal morphology, distribution and behaviour respond to a spectrum of signals, from intracellular signalling to global climatic change. Such concerted adaptation results from a web of control systems, reminiscent of a 'scale-free' network, whose untangling requires integrated approaches beyond those currently used.

http://www.bio.bristol.ac.uk/research/HetheringtonLab/pdfs/nature01843.pdf

The role of stomata in sensing and driving environmental change.

Communities of microscopic plant life, or phytoplankton, dominate the Earth's aquatic ecosystems. This important new book by Colin Reynolds covers the adaptations, physiology and population dynamics of phytoplankton communities in lakes and rivers and oceans. It provides basic information on composition, morphology and physiology of the main phyletic groups represented in marine and freshwater systems and in addition reviews recent advances in community ecology, developing an appreciation of assembly processes, co-existence and competition, disturbance and diversity. Although focussed on one group of organisms, the book develops many concepts relevant to ecology in the broadest sense, and as such will appeal to graduate students and researchers in ecology, limnology and oceanography.

/pdf/the-ecology-of-phytoplankton-4ev70n3jsq.pdf

The Ecology of Phytoplankton

Large areas of the lower epidermis of full-grown leaves of Polypodium vulgare (and Valerianella locusta) are normally separated from the mesophyll by an extensive subepidermal airspace. Epidermal stripes were prepared for experiments to simulate these conditions in order to investigate stomatal reactions. They were placed with their inner surface in contact with an airspace of uniformly high humidity. The outer surface was treated with air of varying degrees of humidity. The stomatal reactions were observed by microscope and the opening of the guard cells determined photographically. Treatment of the outer side of the epidermis with dry air led to a rapid closing of the stomata, whilst moist air caused opening. This induction of opening and closing movements could be repeated up to 15 times with the same stoma by changing the degree of humidity. Neighbouring groups of stomata showed different apertures according to their individual humidity conditions. The degree of aperture of the stomata depended on the water potential of the ambient air and also on the humidity conditions in the subepidermal airspace. The cause of this stomatal behaviour could lie in the “peristomatal transpiration”. In this way, the guard cells are able to function as “humidity sensors” which “measure” the difference in water potential inside and outside the leaf. Their aperture thus is controlled by their individual transpiration conditions. This controlling mechanism could be very important for the water economy of plants. They would appear to be able to reduce their transpiration through an increase in diffusion resistance of the stomata during decreasing humidity in the ambient air, without changing the water status of the whole leaf.

Responses of stomata to changes in humidity.

Water and Plant Life

Publisher Summary This chapter illustrates the physiological and morphological responses of lichens to extreme environmental stresses, which include drought and desiccation, wetness, temperature, humidity, visible or ionizing radiation, gamma irradiation, radioactive materials, and mechanical influences. The drought resistance of lichen is directly correlated to the intensity of desiccation (relative humidity) and to the length of the desiccation period. The stimulation of respiration after desiccation stress causes considerable loss of carbohydrates. Photosynthesis increases spontaneously with water vapor intake at a relative humidity below 100%. Further, the desiccation resistance varies according to species. The comparative analyses of resistance to submersion shown by terrestrial and aquatic lichens clearly demonstrate the ecological importance of the moisture regime for the distribution of lichens. The life of lichen is characterized by rapid changes between active and inactive states. These changes can be optimally profitable if they allow for sufficient time (continuation) and intensity of metabolism, thus, producing biomass. Their resistance allows lichens to persist under environmental stress either in the active state (plasmatic tolerance) or by diminishing the stress in the anabiotic, desiccated state, which is made possible by their poikilohydric nature (constitutional resistance). Lichen can respond to adverse conditions by morphological adjustments, by pigmentation of the thallus, and by changes in the symbiotic state. Erratic lichens in deserts and steppes indicate the ability to be translocated to more favorable environments.

Response to extreme environments

Annual gross productivity of the lichen-dominated cryptoendolithic community was calculated from a computer analysis of photosynthetic response based on laboratory measurements of CO2 exchange and three years (1985-1988) of field nanoclimate data. Photosynthetic optimum increased from -3 to 2 degrees C between irradiance levels of 100 and 1500 micromoles photons m-2 s-1, while the upper compensation point rose from 1 to 17 degrees C. The mean yearly total time available for metabolic activity (temperature above -10 degrees C and moisture present) was 771.3 h for horizontal rock, 421.5 h for northeast-oriented sloped rock, and 1042.2 h for a small depression in horizontal rock (the characteristic site of occasional lichen apothecia). The calculated mean gross productivity value for a horizontal rock was 1215 mg C m-2 y-1, and net photosynthetic gain was 606 mg C m-2 y-1. Net ecosystem productivity (annual accretion of cellular biomass) estimated from long-term events amounted to only about 3 mg C m-2 y-1. The difference between these two values may represent the long-term metabolic costs of the frequent dehydration-rehydration and freezing-thawing cycles or of overwintering, and may account for the leaching of organic substances to the rock. The yearly gross productivity of the cryptoendolithic microbial community of the entire Ross Desert area was estimated at approximately 120,000-180,000 kg C. Of this, 600-900 kg C is in microbial biomass, and much of the rest is soluble compounds that leach into the rocks and possibly percolate to the valleys, providing a source of organic matter for lakes, rivers, and soils.

Long-term productivity in the cryptoendolithic microbial community of the Ross Desert, Antarctica.

Experiments with Prunus armeniaca were carried out under conditions of constant temperature but varying air humidity. Experiments were also contucted with a constant water vapor difference between the evaporating sites in a leaf and the air, but with varying leaf temperature. These served as a basis for predicting the daily course of total diffusion resistance under the natural climatic conditions of a desert. For the simulation, the rsults of the experiments at constant conditions with only one variable factor are fitted with empirical equations which serve as "calibration curves" to predict the change in diffusion resistance caused by a change in humidity and temperature calculated from the meteorological data of a desert day. The simulation shows that for P. armeniaca humidity and temperature are the dominating factors in controlling the daily course of diffusion resistance. For meteorologically very different days the simulation allows the increase in diffusion resistance in the morning to be predicted with an accuracy of 90%-105% as compared to directly observed measurements. In the afternoon, especially after extreme climatic conditions during the morning, the deviation between predicted and observed values of diffusion resistance may be greater, but not more than -20% to -30%. This possibly indicates the existence of an additional factor of significance which was not included in the simulation. The two peaked curves of net photosynthesis and transpiration characteristic of plants living under arid conditions can be explained in this species by the humidity-and temperature-controlled stomatal response. This stomatal regulation leads to a decreasing total daily transpirational water loss on a dry day as compared to a moist one. The significance of this controlling mechanism for the primary production and the water relations of P. armeniaca is discussed.

The role of air humidity and leaf temperature in controlling stomatal resistance of Prunus armeniaca L. under desert conditions : I. A simulation of the daily course of stomatal resistance.

Ludger Kappen

Papers

Responses of stomata to changes in humidity.

Water and Plant Life

Response to extreme environments

Long-term productivity in the cryptoendolithic microbial community of the Ross Desert, Antarctica.

The role of air humidity and leaf temperature in controlling stomatal resistance of Prunus armeniaca L. under desert conditions : I. A simulation of the daily course of stomatal resistance.