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Biomedical subjects

S P Long

Publications and source records attributed to S P Long.

13 recordsLinked to original sources
PubMed2006

Can fast-growing plantation trees escape biochemical down-regulation of photosynthesis when grown throughout their complete production cycle in the open air under elevated carbon dioxide?

Poplar trees sustain close to the predicted increase in leaf photosynthesis when grown under long-term elevated CO2 concentration ([CO2]). To investigate the mechanisms underlying this response, carbohydrate accumulation and protein expression were determined over four seasons of growth. No increase in the levels of soluble carbohydrates was observed in the young expanding or mature sun leaves of the three poplar genotypes during this period. However, substantial increases in starch levels were observed in the mature leaves of all three poplar genotypes grown in elevated [CO2]. Despite the very high starch levels, no changes in the expression of photosynthetic Calvin cycle proteins, or in the starch biosynthetic enzyme ADP-glucose pyrophosphorylase (AGPase), were observed. This suggested that no long-term photosynthetic acclimation to CO2 occurred in these plants. Our data indicate that poplar trees are able to 'escape' from long-term, acclimatory down-regulation of photosynthesis through a high capacity for starch synthesis and carbon export. These findings show that these poplar genotypes are well suited to the elevated [CO2] conditions forecast for the middle of this century and may be particularly suited for planting for the long-term carbon sequestration into wood.

Air↗
PubMed2005

Net carbon storage in a poplar plantation (POPFACE) after three years of free-air CO2 enrichment.

A high-density plantation of three genotypes of Populus was exposed to an elevated concentration of carbon dioxide ([CO(2)]; 550 micromol mol(-1)) from planting through canopy closure using a free-air CO(2) enrichment (FACE) technique. The FACE treatment stimulated gross primary productivity by 22 and 11% in the second and third years, respectively. Partitioning of extra carbon (C) among C pools of different turnover rates is of critical interest; thus, we calculated net ecosystem productivity (NEP) to determine whether elevated atmospheric [CO(2)] will enhance net plantation C storage capacity. Free-air CO(2) enrichment increased net primary productivity (NPP) of all genotypes by 21% in the second year and by 26% in the third year, mainly because of an increase in the size of C pools with relatively slow turnover rates (i.e., wood). In all genotypes in the FACE treatment, more new soil C was added to the total soil C pool compared with the control treatment. However, more old soil C loss was observed in the FACE treatment compared with the control treatment, possibly due to a priming effect from newly incorporated root litter. FACE did not significantly increase NEP, probably as a result of this priming effect.

Biomass↗
PubMed2003

Gas exchange measurements, what can they tell us about the underlying limitations to photosynthesis? Procedures and sources of error.

The principles, equipment and procedures for measuring leaf and canopy gas exchange have been described previously as has chlorophyll fluorescence. Simultaneous measurement of the responses of leaf gas exchange and modulated chlorophyll fluorescence to light and CO2 concentration now provide a means to determine a wide range of key biochemical and biophysical limitations on photo synthesis in vivo. Here the mathematical frameworks and practical procedures for determining these parameters in vivo are consolidated. Leaf CO2 uptake (A) versus intercellular CO2 concentration (Ci) curves may now be routinely obtained from commercial gas exchange systems. The potential pitfalls, and means to avoid these, are examined. Calculation of in vivo maximum rates of ribulose-1,5-bisphosphate (RuBP) carboxylase/oxygenase (Rubisco) carboxylation (Vc,max), electron transport driving regeneration of RuBP (Jmax), and triose-phosphate utilization (VTPU) are explained; these three parameters are now widely assumed to represent the major limitations to light-saturated photosynthesis. Precision in determining these in intact leaves is improved by the simultaneous measurement of electron transport via modulated chlorophyll fluorescence. The A/Ci response also provides a simple practical method for quantifying the limitation that stomata impose on CO2 assimilation. Determining the rate of photorespiratory release of oxygen (Rl) has previously only been possible by isotopic methods, now, by combining gas exchange and fluorescence measurements, Rl may be determined simply and routinely in the field. The physical diffusion of CO2 from the intercellular air space to the site of Rubisco in C3 leaves has long been suspected of being a limitation on photosynthesis, but it has commonly been ignored because of the lack of a practical method for its determination. Again combining gas exchange and fluorescence provides a means to determine mesophyll conductance. This method is described and provides insights into the magnitude and basis of this limitation.

Botany↗
PubMed2003

The role of herbicides in the erosion of salt marshes in eastern England.

Laboratory studies and field trials were conducted to investigate the role of herbicides on saltmarsh vegetation, and their possible significance to saltmarsh erosion. Herbicide concentrations within the ranges present in the aquatic environment were found to reduce the photosynthetic efficiency and growth of both epipelic diatoms and higher saltmarsh plants in the laboratory and in situ. The addition of sublethal concentrations of herbicides resulted in decreased growth rates and photosynthetic efficiency of diatoms and photosynthetic efficiency of higher plants. Sediment stability also decreased due to a reduction in diatom EPS production. There was qualitative evidence that diatoms migrated deeper into the sediment when the surface was exposed to simazine, reducing surface sediment stability by the absence of a cohesive biofilm. Sediment loads on leaves severely reduced photosynthesis in Limonium vulgare. This, coupled with reduced carbon assimilation from the effects of herbicides, could have large negative consequences for plant productivity and over winter survival of saltmarsh plants. The data support the hypothesis that sublethal herbicide concentrations could be playing a role in the increased erosion of salt marshes that has occurred over the past 40 years.

Analysis of Variance↗
PubMed2003

The clonal structure of Quercus geminata revealed by conserved microsatellite loci.

The scrub oak communities of the southeastern USA may have existed at their present locations for thousands of years. These oaks form suckers, and excavations of root systems suggest that clones may occupy very large areas. Resolution of the clonal nature of scrub oaks is important both to manage the tracts of this ecosystem that remain, and in conducting long-term ecological studies, where the study area must substantially exceed the area occupied by any single clone. Microsatellites were used to determine the genetic diversity of a dominant oak species within a 2-ha long-term experimental site on Merritt Island at the Kennedy Space Center. This area contains a long-term study of the effects of elevated CO2 on the ecosystem. Conservation of seven microsatellite loci, previously identified in the sessile oak, Quercus petraea, was tested in two Florida scrub oak species, Q. geminata and Q. myrtifolia. Sequence analysis revealed that all seven microsatellite loci were conserved in Q. geminata and five loci were conserved in Q. myrtifolia. Six microsatellite loci were polymorphic in Q. geminata and these were subsequently used to investigate the clonal structure of the Q. geminata population. Twenty-one unique combinations of microsatellites, or haplotypes, occurred only once, whereas the remaining 26 individuals belonged to a total of seven different haplotypes. Trees with identical haplotypes were in close proximity, supporting the interpretation that they were clones. The results showed that there is significant genetic diversity within the 2-ha experimental site. Microsatellites provided a powerful and noninvasive tool for distinguishing individual genotypes and determining an adequate area for long-term ecosystem studies.

Base Sequence↗
PubMed2001

Small decreases in SBPase cause a linear decline in the apparent RuBP regeneration rate, but do not affect Rubisco carboxylation capacity.

The response of net photosynthetic CO(2) uptake (A) to increasing leaf intercellular CO(2) concentration (c(i)) was determined in antisense Nicotiana tabacum plants, derived from six independent transformation lines, displaying a range of sedoheptulose-1, 7-bisphosphatase (SBPase) activities. The maximum in vivo ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) carboxylation (V(c,max)) and RuBP regeneration (J(max)) rates were calculated from the steady-state measurements of the A to c(i) response curves. In plants with reductions in SBPase activity of between 9% and 60%, maximum RuBP regeneration capacity declined linearly (r(2)=0.79) and no significant change in apparent in vivo Rubisco activity (V(c,max)) was observed in these plants. No correlation between V(c,max) and a decrease in capacity for RuBP regeneration was observed (r(2)=0.14) in the SBPase antisense plants. These data demonstrate that small decreases in SBPase activity limit photosynthetic carbon assimilation by reducing the capacity for RuBP regeneration.

Carbon Dioxide↗
PubMed2001

Growth in elevated CO(2) can both increase and decrease photochemistry and photoinhibition of photosynthesis in a predictable manner. Dactylis glomerata grown in two levels of nitrogen nutrition.

Biochemically based models of C(3) photosynthesis can be used to predict that when photosynthesis is limited by the amount of Rubisco, increasing atmospheric CO(2) partial pressure (pCO(2)) will increase light-saturated linear electron flow through photosystem II (J(t)). This is because the stimulation of electron flow to the photosynthetic carbon reduction cycle (J(c)) will be greater than the competitive suppression of electron flow to the photorespiratory carbon oxidation cycle (J(o)). Where elevated pCO(2) increases J(t), then the ratio of absorbed energy dissipated photochemically to that dissipated non-photochemically will rise. These predictions were tested on Dactylis glomerata grown in fully controlled environments, at either ambient (35 Pa) or elevated (65 Pa) pCO(2), and at two levels of nitrogen nutrition. As was predicted, for D. glomerata grown in high nitrogen, J(t) was significantly higher in plants grown and measured at elevated pCO(2) than for plants grown and measured at ambient pCO(2). This was due to a significant increase in J(c) exceeding any suppression of J(o). This increase in photochemistry at elevated pCO(2) protected against photoinhibition at high light. For plants grown at low nitrogen, J(t) was significantly lower in plants grown and measured at elevated pCO(2) than for plants grown and measured at ambient pCO(2). Elevated pCO(2) again suppressed J(o); however growth in elevated pCO(2) resulted in an acclimatory decrease in leaf Rubisco content that removed any stimulation of J(c). Consistent with decreased photochemistry, for leaves grown at low nitrogen, the recovery from a 3-h photoinhibitory treatment was slower at elevated pCO(2).

Acclimatization↗
PubMed1997

Pain management.

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Chronic Disease↗
PubMed1995

WIMOVAC: a software package for modelling the dynamics of plant leaf and canopy photosynthesis.

The ability to predict net carbon exchange and production of vegetation in response to predicted atmospheric and climate change is critical to assessing the potential impacts of these changes. Mathematical models provide an important tool in the study of whole plant, canopy and ecosystem responses to global environmental change. Because this requires prediction beyond experience, mechanistic rather than empirical models are needed. The uniformity and strong understanding of the photosynthetic process, which is the primary point of response of plant production to global atmospheric change, provides a basis for such an approach. Existing modelling systems have been developed primarily for expert modellers and have not been easily accessible to experimentalists, managers and students. Here we describe a modular modelling system operating within Windows to provide this access. WIMOVAC (Windows Intuitive Model of Vegetation response to Atmosphere and Climate Change) is designed to facilitate the modelling of various aspects of plant photosynthesis with particular emphasis on the effects of global climate change. WIMOVAC has been designed to run on IBM PC-compatible computers running Microsoft Windows. The package allows the sophisticated control of the simulation processes for photosynthesis through a standardized Windows user interface and provides automatically formatted results as either tabulated data or as a range of customizable graphs. WIMOVAC has been written in Microsoft Visual Basic, to facilitate the rapid development of user-friendly modules within the familiar Windows framework, while allowing a structured development. The highly interactive nature of controls adopted by WIMOVAC makes it suitable for research, management and educational purposes.

Algorithms↗
PubMed1991

The Sequence of Change within the Photosynthetic Apparatus of Wheat following Short-Term Exposure to Ozone.

The basis of inhibition of photosynthesis by single acute O(3) exposures was investigated in vivo using analyses based on leaf gas exchange measurements. The fully expanded second leaves of wheat plants (Triticum aestivum L. cv Avalon) were fumigated with either 200 or 400 nanomoles per mole O(3) for between 4 and 16 hours. This reduced significantly the light-saturated rate of CO(2) uptake and was accompanied by a parallel decrease in stomatal conductance. However, the stomatal limitation, estimated from the relationship between CO(2) uptake and the internal CO(2) concentration, only increased significantly during the first 8 hours of exposure to 400 nanomoles per mole O(3); no significant increase occurred for any of the other treatments. Analysis of the response of CO(2) uptake to the internal CO(2) concentration implied that the predominant factor responsible for the reduction in light-saturated CO(2) uptake was a decrease in the efficiency of carboxylation. This was 58 and 21% of the control value after 16 hours at 200 and 400 nanomoles per mole O(3), respectively. At saturating concentrations of CO(2), photosynthesis was inhibited by no more than 22% after 16 hours, indicating that the capacity for regeneration of ribulose bisphosphate was less susceptible to O(3). Ozone fumigations also had a less pronounced effect on light-limited photosynthesis. The maximum quantum yield of CO(2) uptake and the quantum yield of oxygen evolution showed no significant decline after 16 hours with 200 nanomoles per mole O(3), requiring 8 hours at 400 nanomoles per mole O(3) before a significant reduction occurred. The photochemical efficiency of photosystem II estimated from the ratio of variable to maximum chlorophyll fluorescence and the atrazine-binding capacity of isolated thylakoids demonstrated that photochemical reactions were not responsible for the initial inhibition of CO(2) uptake. The results suggest that the apparent carboxylation efficiency appears to be the initial cause of decline in photosynthesis in vivo following acute O(3) fumigation.

Journal Article↗
PubMed1991

Effect of the Long-Term Elevation of CO(2) Concentration in the Field on the Quantum Yield of Photosynthesis of the C(3) Sedge, Scirpus olneyi.

CO(2) concentration was elevated throughout 3 years around stands of the C(3) sedge Scirpus olneyi on a tidal marsh of the Chesapeake Bay. The hypothesis that tissues developed in an elevated CO(2) atmosphere will show an acclimatory decrease in photosynthetic capacity under light-limiting conditions was examined. The absorbed light quantum yield of CO(2) uptake (ø(abs) and the efficiency of photosystem II photochemistry were determined for plants which had developed in open top chambers with CO(2) concentrations in air of 680 micromoles per mole, and of 351 micromoles per mole as controls. An Ulbricht sphere cuvette incorporated into an open gas exchange system was used to determine ø(abs) and a portable chlorophyll fluorimeter was used to estimate the photochemical efficiency of photosystem II. When measured in an atmosphere with 10 millimoles per mole O(2) to suppress photorespiration, shoots showed a ø(abs) of 0.093 +/- 0.003, with no statistically significant difference between shoots grown in elevated or control CO(2) concentrations. Efficiency of photosystem II photochemistry was also unchanged by development in an elevated CO(2) atmosphere. Shoots grown and measured in 680 micromoles per mole of CO(2) in air showed a ø(abs) of 0.078 +/- 0.004 compared with 0.065 +/- 0.003 for leaves grown and measured in 351 micromoles per mole CO(2) in air; a highly significant increase. In accordance with the change in ø(abs), the light compensation point of photosynthesis decreased from 51 +/- 3 to 31 +/- 3 micro-moles per square meter per second for stems grown and measured in 351 and 680 micromoles per mole of CO(2) in air, respectively. The results suggest that even after 3 years of growth in elevated CO(2), there is no evidence of acclimation in capacity for photosynthesis under light-limited conditions which would counteract the stimulation of photosynthetic CO(2) uptake otherwise expected through decreased photorespiration.

Journal Article↗
PubMed1988

Photosynthesis and temperature, with particular reference to effects on quantum yield.

Previous reviews of the effects of temperature on in vivo photosynthesis have mainly concerned the effects of temperature on light saturated rates. The quantum yield of photosynthesis (phi), as a measure of light limited photosynthesis, has generally been regarded as temperature insensitive. At temperatures close to the minima and maxima at which plants can sustain photosynthetic CO2 assimilation, light may damage the photosynthetic apparatus, an effect termed photoinhibition. A constant feature of photoinhibition is a reduction in phi. In maize, chilling-dependent photoinhibition reduces both phi and the light saturated rate of CO2 assimilation (Asat) and of O2 evolution. Analysis of recovery of CO2 uptake in these leaves suggests that whilst Asat recovers in a few hours, phi may not be fully restored for days. Examination of mature crop canopies shows that only a small proportion of the leaves are likely to become light saturated and then only for part of the day. The relative significance of temperature-induced changes in Asat and phi have also been tested in canopy models of maize crop photosynthesis. These suggest that whilst changes in either parameter will have similar effects on total canopy photosynthesis on the sunniest days of the year, for an average summer's day changes in phi will be of far greater importance. Consideration is therefore given to the factors associated with thylakoid membranes that may determine temperature-induced decreases in phi. Chilling of maize leaves under high light levels reduces the quantum yield of PSII and whole chain electron transport in concert with a decrease in the capacity of isolated thylakoids to bind atrazine, which is indicative of a loss or damage to the QB protein. Besides such classical symptoms of photoinhibition of PSII, chilling also induces the accumulation of a 31 kDa polypeptide in the thylakoids of maize leaves. This polypeptide fractionates with the light-harvesting chlorophyll a/b protein complex (LHCII) and has been tentatively identified as an unprocessed precursor of CP29 since it binds chlorophyll and is immunologically related to CP29. Accumulation of the 31 kDa polypeptide is associated with a modification in the energetics of LHCII, which may result in a decrease in excitation energy from LHCII to PSII and contribute to a decrease in phi. Examination is also made of how stress-induced modifications of interactions between PSII complexes, functioning of the cyt b6/f complex, the permeability of the thylakoid membrane to protons and the activity of the coupling factor may contribute to decreases in phi.

Cold Temperature↗