273 research outputs found

    Changes in New Zealand pan evaporation since the 1970s,

    Get PDF
    ABSTRACT Several previous studies have reported declines in pan evaporation rate throughout the Northern Hemisphere of about 2-4 mm a −2 for various periods since the 1950s. A recent analysis of Australian pan evaporation reported a similar decline and raises the possibility that part of the phenomenon may be related to the greenhouse effect. To assess that possibility, one needs to know whether the decline in evaporative demand is happening in other parts of the Southern Hemisphere. As a first step to addressing the latter question, we examined the trend in pan evaporation at 19 New Zealand sites. We found statistically significant declines in pan evaporation rate at 6 of the 19 sites. There were no sites with statistically significant increases in pan evaporation. When averaged across all 19 sites, the decline in pan evaporation rate was roughly 2 mm a −2 (i.e. mm per annum per annum) since the 1970s. Over a 30-year period, this is equivalent to a decline of about 60 mm a −1 in annual pan evaporation. These results are generally consistent with those reported throughout the Northern Hemisphere and in Australia. We conclude that the trend for decreasing evaporative demand previously reported throughout the Northern Hemisphere terrestrial surface may also be widespread in the Southern Hemisphere. This may be, in part, a greenhouse-related phenomenon

    On the extent of genetic variation for transpiration efficiency in sorghum

    Get PDF
    A glasshouse study examined 49 diverse sorghum lines for variation in transpiration efficiency. Three of the 49 lines grown were Sorghum spp. native to Australia; one was the major weed Johnson grass (Sorghum halepense), and the remaining 45 lines were cultivars of Sorghum bicolor. All plants were grown under non-limiting water and nutrient conditions using a semi-automatic pot watering system designed to facilitate accurate measurement of water use. Plants were harvested 56–58 days after sowing and dry weights of plant parts were determined. Transpiration efficiency differed signficantly among cultivars. The 3 Australian native sorghums had much lower transpiration efficiency than the other 46 cultivars, which ranged from 7·7 to 6·0 g/kg. For the 46 diverse cultivars, the ratio of range in transpiration efficiency to its l.s.d. was 2·0, which was similar to that found among more adapted cultivars in a previous study. This is a significant finding as it suggests that there is likely to be little pay-off from pursuing screening of unadapted material for increased variation in transpiration efficiency. It is necessary, however, also to examine absolute levels of transpiration efficiency to determine whether increased levels have been found. The cultivar with greatest transpiration efficiency in this study (IS9710) had a value 9% greater (P < 0·05) than the accepted standard for adapted sorghum cultivars. The potential impact of such an increase in transpiration efficiency warrants continued effort to capture it. Transpiration efficiency has been related theoretically and experimentally to the degree of carbon isotope discrimination in leaf tissue in sorghum, which thus offers a relatively simple selection index. In this study, the variation in transpiration efficiency was not related simply to carbon isotope discrimination. Significant associations of transpiration efficiency with ash content and indices of photosynthetic capacity were found. However, the associations were not strong. These results suggest that a simple screening technique could not be based on any of the measures or indices analysed in this study. A better understanding of the physiological basis of the observed genetic differences in transpiration efficiency may assist in developing reliable selection indices. It was concluded that the potential value of the improvement in transpiration efficiency over the accepted standard and the degree of genetic variation found warrant further study on this subject. It was suggested that screening for genetic variation under water-limiting conditions may provide useful insights and should be pursued

    Effects of rising temperatures and [CO2] on the physiology of tropical forest trees

    Get PDF
    Using a mixture of observations and climate model outputs and a simple parametrization of leaf-level photosynthesis incorporating known temperature sensitivities, we find no evidence for tropical forests currently existing ‘dangerously close’ to their optimum temperature range. Our model suggests that although reductions in photosynthetic rate at leaf temperatures (TL) above 30°C may occur, these are almost entirely accountable for in terms of reductions in stomatal conductance in response to higher leaf-to-air vapour pressure deficits D. This is as opposed to direct effects of TL on photosynthetic metabolism. We also find that increases in photosynthetic rates associated with increases in ambient [CO2] over forthcoming decades should more than offset any decline in photosynthetic productivity due to higher D or TL or increased autotrophic respiration rates as a consequence of higher tissue temperatures. We also find little direct evidence that tropical forests should not be able to respond to increases in [CO2] and argue that the magnitude and pattern of increases in forest dynamics across Amazonia observed over the last few decades are consistent with a [CO2]-induced stimulation of tree growth

    Simulating daily field crop canopy photosynthesis: an integrated software package

    Get PDF
    Photosynthetic manipulation is seen as a promising avenue for advancing field crop productivity. However, progress is constrained by the lack of connection between leaf-level photosynthetic manipulation and crop performance. Here we report on the development of a model of diurnal canopy photosynthesis for well watered conditions by using biochemical models of C-3 and C-4 photosynthesis upscaled to the canopy level using the simple and robust sun-shade leaves representation of the canopy. The canopy model was integrated over the time course of the day for diurnal canopy photosynthesis simulation. Rationality analysis of the model showed that it simulated the expected responses in diurnal canopy photosynthesis and daily biomass accumulation to key environmental factors (i.e. radiation, temperature and CO2), canopy attributes (e.g. leaf area index and leaf angle) and canopy nitrogen status (i.e. specific leaf nitrogen and its profile through the canopy). This Diurnal Canopy Photosynthesis Simulator (DCaPS) was developed into a web-based application to enhance usability of the model. Applications of the DCaPS package for assessing likely canopy-level consequences of changes in photosynthetic properties and its implications for connecting photosynthesis with crop growth and development modelling are discussed

    An improved system to measure leaf gas exchange on adaxial and abaxial surfaces

    Get PDF
    Measurement of leaf carbon gain and water loss (gas exchange) in planta is a standard procedure in plant science research for attempting to understand physiological traits related to water use and photosynthesis. Leaves carry out gas exchange through the upper (adaxial) and lower (abaxial) surfaces at different magnitudes, depending on the stomatal density, stomatal aperture, cuticular permeability, etc., of each surface, which we account for in gas exchange parameters such as stomatal conductance. Most commercial devices measure leaf gas exchange by combining the adaxial and abaxial fluxes and calculating bulk gas exchange parameters, missing details of the plant's physiological response on each side. Additionally, the widely used equations to estimate gas exchange parameters neglect the contribution of small fluxes such as cuticular conductance, adding extra uncertainties to measurements performed in water-stress or low-light conditions. Accounting for the gas exchange fluxes from each side of the leaf allows us to better describe plants' physiological traits under different environmental conditions and account for genetic variability. Here, apparatus and materials are presented for adapting two LI-6800 Portable Photosynthesis Systems to work as one gas exchange system to measure adaxial and abaxial gas exchange simultaneously. The modification includes a template script with the equations to account for small fluxes. Instructions are provided for incorporating the add-on script into the device's computational sequence, display, variables, and spreadsheet results. We explain the method to obtain an equation to estimate boundary layer conductance to water for the new setup and how to embed this equation in the devices' calculations using the provided add-on script. The apparatus, methods, and protocols presented here provide a simple adaptation combining two LI-6800s to obtain an improved system to measure leaf gas exchange on adaxial and abaxial surfaces

    Assessing the CO2 concentration at the surface of photosynthetic mesophyll cells

    Get PDF
    We present a robust estimation of the CO2 concentration at the surface of photosynthetic mesophyll cells (cw), applicable under reasonable assumptions of assimilation distribution within the leaf. We used Capsicum annuum, Helianthus annuus and Gossypium hirsutumas model plants for our experiments. We introduce calculations to estimate cw using independent adaxial and abaxial gas exchange measurements, and accounting for the mesophyll airspace resistances. The cw was lower than adaxial and abaxial estimated intercellular CO2 concentrations (ci). Differences between cw and the ci of each surface were usually larger than 10 μmol mol−1. Differences between adaxial and abaxial ci ranged from a few μmol mol−1 to almost 50 μmol mol−1, where the largest differences were found at high air saturation deficits (ASD). Differences between adaxial and abaxial ci and the ci estimated by mixing both fluxes ranged from −30 to +20 μmol mol−1, where the largest differences were found under high ASD or high ambient CO2 concentrations. Accounting for cw improves the information that can be extracted from gas exchange experiments, allowing a more detailed description of the CO2 and water vapor gradients within the leaf

    Oscillations in Stomatal Conductance

    Full text link
    corecore