Peter J.H. Sharpe’s research while affiliated with Texas A&M University and other places

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Publications (72)


An overview of the TAMBEETLE model of Dendroctonus frontalis population dynamics
  • Article

June 2006

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26 Reads

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18 Citations

Robert N. Coulson

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P. J. H. Sharpe

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[...]

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T. L. Payne

Population dynamics of the southern pine beetle Dendroctonus frontalis has been the subject of intensive research in the USA for more than a decade. TAMBEETLE, an acronym for the mechanistic model of population dynamics of D. frontalis, was developed to abstract contemporary knowledge on the insect. This model was developed as a joint venture between the Biosystems Research Group of Industrial Engineering and the Department of Entomology at Texas A&M University. The approach used to develop the model and the structure of component submodels is described. Research leading to the development of the model involved a series of field and laboratory studies aimed at various aspects of the population system of the insect. This research is reviewed. Important areas needing further research are identified. Studies dealing with factors involved in initiation of infestions, biome-level epidemiology, host susceptibility, stand modeling, and dynamics of within-tree mortality were emphasized as important topics for further research.


The role of the epidermal cells in the carbon dioxide response of stomata of Vicia faba L

May 2006

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19 Reads

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4 Citations

S ummary The role of the epidermal cell has rarely been adequately investigated in studies of stomatal movements. In this study of Vicia faba , the changes in aperture in isolated epidermal strips and in intact leaf sections in response to a variety of CO 2 concentrations and temperatures in both light and darkness have been observed for guard cells that were in contact with live epidermal cells. The results indicate that the response of the stomatal system to CO 2 is largely dependent upon the degree to which the guard cell is functionally connected to the rest of the leaf. Stomata of guard cells in contact with live epidermal cells from leaf sections showed a significant decrease in aperture with increased CO 2 . Stomata of guard cells in contact with live epidermal cells on isolated epidermal strips, however, showed an increase in aperture with increased CO 2 which also appears to be related to temperature. Results can be interpreted as supporting the chemiosmotic hypothesis of stomatal movements. The data also indicate that there are two opposing responses in the stomatal system to CO 2 : an opening response located in the epidermis and an overriding closing response controlled by the mesophyll.


Response of guard cells to temperature at different concentrations of carbon dioxide in Vicia faba L

May 2006

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16 Reads

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5 Citations

S ummary One of the least understood areas in guard cell movements remains the effect of CO 2 , particularly its effect on isolated guard cells. In this study the reactions of guard cells in both isolated epidermal strips and intact leaf sections from Vicia faba have been observed in a variety of temperatures and CO 2 concentrations in both light and darkness. The results are consistent with the hypothesis that stomatal aperture in the isolated guard cell is the result of two temperature‐dependent systems. A decrease in aperture consistently observed at 30 to 35°C in the light reflects the transition from one system to the other. The low temperature system appears consistent with the chemiosmotic hypothesis of phosphoenolpyruvate carboxylase regulation of malate. It demonstrates some sensitivity to CO 2 between 25 and 35 °C, resulting in a shift in optimum aperture to slightly higher temperatures. The high temperature system shows no apparent sensitivity to CO 2 . Stomata from intact leaf sections showed a considerable decrease in aperture as the CO 2 concentration increased from 0 to 60 μl 1 ⁻¹ . The stomatal response threshold to CO 2 appears to be at least as low as 60μ1 1 ⁻¹ and centred in the mesophyll tissue. All observable CO 2 responses in both strips and leaf sections disappeared at temperatures in excess of 35 °C in the light.


Stomatal mechanics. III. Geometric interpretation of the mechanical advantage*

April 2006

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49 Reads

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29 Citations

Plant Cell and Environment

Previous mathematical analyses of stomatal mechanics have demonstrated, and experimental measurements have confirmed, that the turgor-generated force of the epidermal cells dominates that of the guard cells in determining aperture. DcMichele & Sharpe (1973) termed the phenomenon the mechanical advantage of the epidermal cells, while Cooke et al. (1976) expressed it as an antagonism ratio. Both of these formulations, however, have theoretical or practical limitations. This study presents a biophysical analysis demonstrating that the effective forces in the stomatal system may be studied in terms of simple stomatal geometry. From this analysis, the mechanical advantage can be redefined and interpreted based upon simple geometric relationships calculated from measurable anatomical dimensions.


Stomatal mechanics II: material properties of guard cell walls

April 2006

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120 Reads

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27 Citations

Plant Cell and Environment

Abstract In this revised formulation of guard cell mechanics, the material properties of the walls are re-examined. The observed elastic anisotropy of guard cell walls can be explained by non-random orientation of the cellulose micellae in the unstrained state. This micellar network is assumed to be loosely embedded in the wall matrix causing a two phase elongation process. In the first phase, the micellar network is ‘loose’ resulting in the walls behaving as an isotropic polymer when stretched. As the volume of the cell expands beyond some threshold, the network becomes ‘tightened’ and a second phase of elongation is initiated. During this anisotropic phase of cell expansion, wall elasticity reflectes changes in the orientation of the network to reduce its load. Using the above theoretical analysis, a turgor-pressure versus lumen volume relationship is simulated for Vicia faba. The relationship between aperture and water potential for this species is also established. The simulated results agree with the experimental evidence reported for Vicia faba. The estimated shear modulus of elasticity for guard cell walls is 2 MPa (20 bars) which is well within the limits of reported values for other biological tissues.


Water stress effects on guard cell anatomy and the mechanical advantage of the epidermal cells

April 2006

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340 Reads

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106 Citations

Plant Cell and Environment

Abstract Vicia faba plants grown under water deficit were found to have guard cells considerably smaller than those of plants grown under well-watered conditions. Stomala of plants adapted to drought conditions have been observed in past studies to maintain opening at plant water potentials lower than those of plants not so adapted. By employing the geometric interpretation of the mechanical advantage (Wu, Sharpe & Spence, 1985), an anatomical/mechanical basis was found that helps explain how such opening in drought conditions can occur. The geometry and resulting mechanical properties of small stomata, in contrast to larger stomata, give them the capability of opening or maintaining open pores with lower guard cell turgor pressures, relative to the turgor of the surrounding epidermal cells.


Generation of mechanistic variability in a process-based object-oriented plant model

June 1993

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10 Reads

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12 Citations

Ecological Modelling

A cotton crop model based on individual plant developmental behavior and variability was developed. Object-oriented simulation (OOS) provided the conceptual basis for the new model structure. The procedural model, COTSIM, provided the theoretical background for cotton plant development. Data collected during 1987 from field-grown cotton were used for model development and verification, and data from 1988 were used for model validation. The model predicted mass accretion and production of organs within the patterns and magnitudes observed in the field. The model also predicted crop development aspects that had not previously been described by procedural models. Age and size of leaves and fruit and associated developmental variability were included in the model through representation of objects and their variable behavior defined by their position on the plant and how this constrains their growth. Observed variability was the result of the aggregate behavior of components. Variability in our OOS model is an output as opposed to being an input in most procedural plant models. The model has recreated both realistic plants and populations in a mechanistic simulation. Object-oriented models are an important step towards common structures and languages for model design and the development of simulations. It was noted that increased mechanistic detail resulted in an increase of procedure calls (messages) and a five-fold increase in model run time.




Object-oriented simulation: plant growth and discrete organ-to-organ interaction

November 1991

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25 Reads

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67 Citations

Ecological Modelling

This paper reviews and applies new hierarchical approaches to ecological modelling. These new approaches are made possible by the development of the object-oriented paradigm. This paradigm draws upon the notion of ‘universal’ or classes dating back to early Greek philosophy. It is an intriguing approach to simulation because it is based upon the concepts of hierarchy and taxonomy, two of the basic organizing principles in ecology. Adopting an object-oriented approach to simulation can result in a reduction of mathematical and statistical abstraction. The object-oriented approach lends itself directly to incorporation of mechanisms within appropriate hierarchies.


Citations (69)


... The kidney-shaped guard cells of angiosperms open each stomatal pore by changing contour along the vertical/transversal axis, as well as by outward movement of dorsal walls into adjacent cells (Fig. 2d;Sharpe et al., 1987;Franks & Farquhar, 2007). This lateral movement depends on radially oriented fibres that strengthen the guard cell walls and/or pectin-based mechanical restrictions at the polar ends of these cells (Carter et al., 2017). ...

Reference:

On the origins of osmotically driven stomatal movements
Stomatal mechanics
  • Citing Article
  • January 1987

... It is often suitable where conditions of strict randomness of the exponential distribution are not satisfied [8]. The Weibull has been used by several authors for analyzing and describing seed germination [6,7,9]. The function's parameters are biologically interpretable, reflecting maximum germination (M), germination rate (K), lag in onset of germination (L), and the shape of the cumulative distribution (C). ...

Modeling Distributions of Crop and Weed Seed Germination Time
  • Citing Article
  • September 1989

Weed Science

... If not controlled, spots may grow to encompass new trees at rates of a few to dozensin extreme cases, hundredsper week (Hedden and Billings 1979;Clarke and Billings 2003). Southern pine beetle spot infestations typically are initiated in the spring (Coulson et al. 1985;Ayres et al. 2011;Martinson et al. 2013) and often start in single trees or small groups of trees weakened by lightning strike (Hodges and Pickard 1971;Coulson et al. 1983). They may continue to accumulate infested trees along their margin throughout the summer and early fall (Thatcher and Pickard 1964;Franklin 1970). ...

Population dynamics of initiation and growth of southern pine beetle infestations
  • Citing Article
  • January 1985

... While light intensity experiments are carried out with adequate light and appropriate temperature conditions, dark experiments require a supply of ATP and a reducing agent [H] (Jagendorf, 1963). Young (new bud) leaves formed under 0 µmol m − 2 •s − 1 by a dark reaction process (Sharpe, 1983), while at 31 µmol m − 2 •s -1 to 411 µmol m − 2 •s − 1 , young leaves were synthesized autonomously by photoreactive processes (Miller & Urey, 1959). ...

Responses of Photosynthesis and Dark Respiration to Temperature
  • Citing Article
  • September 1983

Annals of Botany

... The modeled response mechanism of carbon allocation to environmental changes remains unclear. Theoretically, the dynamic characteristics of plant carbon allocation result from their response in terms of using carbon to capture the most limiting resources (e.g., light, water, and nutrients) (Sharpe and Rykiel 1991;Kobe et al. 2010). The limitation of critical resources, such as water and nutrients, can enhance carbon allocation to the roots of plants to increase their uptake and alleviate resource deficits (Ikegami et al. 2007;Matzek 2011;Peng et al. 2017;Brunn et al. 2022). ...

Modelling Integrated Response of Plants to Multiple Stresses
  • Citing Chapter
  • December 1991

... However, osmotic adjustments observed in infested Bing and Van trees apparently were not involved in maintaining cell turgor because J L min was about 1.5 MPa higher (less negative) than the osmotic potential at the turgor loss point (p 0 ) and thus cell turgor loss is unlike to occur in all cultivars. We hypothesized that osmotic adjustment in defoliated trees of Van and Bing cultivars is an anti-herbivory response related to the production of chemical compounds to deter herbivores (Sharpe et al., 1986). ...

Forest Pests: The Role of Phloem Osmotic Adjustment in the Defensive Response of Conifers to Bark Beetle Attack
  • Citing Chapter
  • January 1986

... Upon examination of the existing mechanistic models defining each of these parts, it was found that only two of the above parts had been described by physiologically-based models. Steady-state source models have been developed by Sharpe and DeMichele (1974), Charles-Edwards and Ludwig (1974) and DeMichele et al. (1978). A steady-state model of the movement of sucrose along the path region has been developed by Goeschl et al. (1976). ...

A Morphological and Physiological Model of the Leaf
  • Citing Article
  • January 1974

Transactions of the ASAE. American Society of Agricultural Engineers

... tion data using an empirically determined pan factor, which was a function of the leaf area index as given by Wierenga (1983). During 1982 were scheduled on the basis of the reference crop evapotranspiration determined from pan evaporation (Doorenbos and Pruitt, 1977 ), with help of the crop coefficients for chile peppers determined by Saddiq (1983). In 1977, water treatments were applied directly after planting. From 1979 on, treatments were started after a good stand was obtained, usually about 80 days after planting. Before each treatment began, the plots were usually irrigated once a week. After treatments began, all plots were irrigated three times per week in the years 1979 through 19 ...

The Influence of Trickle Irrigation on the Quality of Irrigation Return Flow
  • Citing Article

... Clearing of woodlands generally promotes grass growth (Walker et al. 1972(Walker et al. , 1986, primarily by increasing insolation to ground-layer vegetation (Specht and Morgan 1981). However, while there are typically substantial increases in pasture biomass in the short-term, longer-term studies suggest that these gains may not be sustainable over longer time frames (> 20 years) due to nutrient rundown (Kaur et al. 2005;Sangha et al. 2005a;). ...

Herbage response to tree thinning in a Eucalyptus cebra woodland
  • Citing Article
  • June 1986

Austral Ecology