Comparative CO2 exchange patterns in mosses from two tundra habitats at Barrow, Alaska

1976 ◽  
Vol 54 (12) ◽  
pp. 1355-1369 ◽  
Author(s):  
Walter C. Oechel ◽  
Nigel J. Collins
Keyword(s):  
Light Intensity ◽  
Water Content ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Co2 Exchange ◽  
Polar Regions ◽  
Light Intensities ◽  
Matter Production ◽  
Exchange Patterns

The effects of variation in light intensity, temperature, and water content on rates of net photosynthesis and dark respiration have been investigated in two common tundra mosses, Polytrichum alpinum from drier habitats and Calliergon sarmentosum from wetter habitats at Barrow, Alaska. Optimum temperatures for net photosynthesis of 10–15 °C for both species and saturating light intensities (photosynthetically active radiation (PhAR), 400–700 nm) of about 0.12 cal cm−2 min−1 for P. alpinum and 0.15 cal cm−2 min−1 for C. sarmentosum correlate well with measurements of light intensity and moss tissue temperatures made over the season at the collection site. It is suggested that depressions in net photosynthetic rates around midday might be caused by supraoptimal temperatures and possibly supraoptimal light intensities. Calliergon sarmentosum, a semiaquatic species required a higher water content (about 450% dry weight) than P. alpinum (about 200%) to reach maximal rates of net photosynthesis. Mean maximal rates of net photosynthesis ranged from about 2.6 to 4.4 mg CO2 g−1 dry weight h−1 for P. alpinum and from about 1.5 to 3.0 mg CO2 g−1 dry weight h−1 for C. sarmentosum. Predictions of net annual production have been made for both species. Predicted levels of 171 g C m−2 per 50-day season for C. sarmentosum compare well with results obtained for species of similar growth form elsewhere in polar regions. For P. alpinum the predicted level of 38.5 g C m−2 per 50-day season compares with observed dry matter production at the same site of 43 g m−2 per season.

scholarly journals Growth reactions of carnation, measured by net photosynthesis, on different air contents of the soil.

1970 ◽  
Vol 18 (3) ◽  
pp. 149-157
Author(s):  
A.L.M. Van Wijk ◽  
J. Buitendijk
Keyword(s):  
Light Intensity ◽  
Dry Matter ◽  
Dianthus Caryophyllus ◽  
Net Photosynthesis ◽  
Constant Level ◽  
Fresh Matter ◽  
Soil Air ◽  
Air Content ◽  
Light Intensities ◽  
Matter Production

In pot experiments, Dianthus caryophyllus plants grown for 2 1/2 months at soil-air levels of 20, 10 or 5% (v/v) produced approx. equal amounts of dry matter, but fresh-matter production at 5 and 10% soil air was 13 and 2% lower than at 20% soil air. The effect of aeration on growth (photosynthesis) increased with increasing light intensity. Decreasing content of soil air from 20, 10 and 5% to 5 and 2.5% respectively was accompanied by an immediate reduction of photosynthesis to a fairly constant level. This reduction increased with increasing light intensity. An increase in soil air from 2.5 to 20, 10 or 5% gave a recovery of photosynthesis which at the two lowest light intensities was complete within 1-3 days when the period of low air content was not >14 days. At the highest light intensity the recovery of photosynthesis was slower. (Abstract retrieved from CAB Abstracts by CABI’s permission)

Photosynthetic Performance of Two Closely Related Umbilicaria Species in Central Spain: Temperature as a Key Factor

1997 ◽  
Vol 29 (1) ◽  
pp. 67-82 ◽  
Author(s):  
L. G. Sancho ◽  
B. Schroeter ◽  
F. Valladares
Keyword(s):  
Water Content ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Distribution Patterns ◽  
Photon Flux ◽  
Photosynthetic Response ◽  
Central Spain ◽  
Natural Conditions ◽  
Thallus Water Content

AbstractNet photosynthesis (NP) and dark respiration (DR) of thalli of the lichen species Umbilicaria grisea and U. freyi growing together in the same habitat the Sierra de Guadarrama, central Spain, were measured under controlled conditions in the laboratory and under natural conditions in the field over a range of photosynthetic photon flux densities (PPFD), thallus temperatures and thallus water contents. Laboratory experiments revealed that the photosynthetic response to PPFD at optimum thallus water content is very similar in both species. The light compensation points of NP increased from PPFD of c. 20 µmol m−2 s−1 at 0°C up to c. 100 µmol m−2 s−1 PPFD at 25°C. In both species light saturation was not reached up to 700 µmol m−2 s−1 PPFD except at 0°C. By contrast, the temperature dependence of CO2 gas exchange differed substantially between U. grisea and U. freyi. Both species gave significant rates at 0°C. Optimal temperatures of NP were always higher in U. grisea at various PPFD levels if the samples were kept at optimal thallus water content. NP showed maximal rates at 95% dw in U. grisea and 110% dw in U. freyi respectively. In U. grisea a much stronger depression of NP was observed with only 5% of maximal NP reached at 180% dw. At all PPFD and temperature combinations U. freyi showed higher rates of NP and more negative rates of DR if calculated on a dry weight basis. This was also true under natural conditions at the same site, when U. freyi was always more productive than U. grisea. The differences in the photosynthetic response to temperature between both species correlated well with the different distribution patterns of both species. The possibility of genetic control of the physiological performance of these species and its influence on their distribution patterns and autecology is discussed.

scholarly journals On the Minimum Quantum Requirement of Photosynthesis

2009 ◽  
Vol 64 (9-10) ◽  
pp. 673-679 ◽  
Author(s):  
Yuzeir Zeinalov
Keyword(s):  
Light Intensity ◽  
Oxygen Evolution ◽  
Quantum Efficiency ◽  
Optical Density ◽  
Dark Respiration ◽  
Linear Part ◽  
Light Curves ◽  
Quantum Requirement ◽  
Light Intensities ◽  
Maximum Quantum Efficiency

An analysis of the shape of photosynthetic light curves is presented and the existence of the initial non-linear part is shown as a consequence of the operation of the non-cooperative (Kok’s) mechanism of oxygen evolution or the effect of dark respiration. The effect of nonlinearity on the quantum efficiency (yield) and quantum requirement is reconsidered. The essential conclusions are: 1) The non-linearity of the light curves cannot be compensated using suspensions of algae or chloroplasts with high (>1.0) optical density or absorbance. 2) The values of the maxima of the quantum efficiency curves or the values of the minima of the quantum requirement curves cannot be used for estimation of the exact value of the maximum quantum efficiency and the minimum quantum requirement. The estimation of the maximum quantum efficiency or the minimum quantum requirement should be performed only after extrapolation of the linear part at higher light intensities of the quantum requirement curves to “0” light intensity

Productivity of Vegetable Crops in a Region of High Solar Input. III. Carbon Balance of Potato Crops

1974 ◽  
Vol 1 (2) ◽  
pp. 283 ◽  
Author(s):  
PJM Sale
Keyword(s):  
Carbon Balance ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Gas Analysis ◽  
Co2 Uptake ◽  
Co2 Efflux ◽  
Vegetable Crops ◽  
Weight Changes ◽  
Potato Crops

The carbon balance of potato crops has been studied by measuring canopy net photosynthesis and dark respiration losses with a field assimilation chamber and semi-closed gas analysis system. Results are given for the latter part of growth in both a spring-planted and a summer-planted crop. Net CO2 uptake increased with solar input to reach 35–40mg dm-2 (ground area) h-1 at 400–450 W m-2, but light saturation then occurred and little or no further uptake resulted from increases in solar input up to 1000 W m-2. This supports the previous conclusion that net photosynthesis in the potato is determined by the size of the 'sink' provided by the developing tubers. The imposed experimental variables of reduced solar input (21 and 34% shade) and soil moisture were found not to affect the relation between solar input and CO2 uptake, and the effect of chamber temperature was also very small. Dark respiration rates of the canopy were markedly sensitive to temperature, and also to the solar input prior to measurement. Respiration from the below-ground plant parts accounted for a considerable part of the total plant respiration. In all, 15–20 % of the net assimilation during daylight hours was lost by night respiration. There was little variation in CO2 efflux from uncropped soil during the experiments. Dry weight changes calculated from the gasometric measurements were in accordance with those found from previous growth analysis. * Part II, Aust. J. Agric. Res., 1973, 24, 751–62.

AN ANALYSIS OF DRY MATTER PRODUCTION OF DOUGLAS-FIR SEEDLINGS IN RELATION TO TEMPERATURE AND LIGHT INTENSITY

1967 ◽  
Vol 45 (11) ◽  
pp. 2063-2072 ◽  
Author(s):  
Holger Brix
Keyword(s):  
Light Intensity ◽  
Leaf Area ◽  
Dry Matter ◽  
Douglas Fir ◽  
Dry Matter Production ◽  
Dry Matter Distribution ◽  
Pronounced Increase ◽  
Light Intensities ◽  
Matter Production ◽  
Net Assimilation

Seedlings of Douglas fir (Pseudotsuga menziesii (Mirb.) Franco) were grown in growth chambers under all combinations of three temperatures (13, 18, and 24 °C) and three light intensities (450, 1000, and 1800 ft-c). Dry matter production of leaves, stem, and roots was determined at 65 and 100 days after germination. The leaf area produced per unit of leaf dry weight and the dry matter distribution to the plant organs was measured. Net assimilation rates between the ages of 65 and 100 days were calculated. Rates of photosynthesis per unit of leaf were determined at different light intensities and temperatures, and rates of respiration of plant top and of roots were found for different temperatures.Increasing light intensity affected dry matter production in two opposing ways: (i) it increased the rate of photosynthesis per unit leaf area, and (ii) it decreased the leaf area added per unit of dry matter produced. A pronounced increase in growth with increase in temperature from 13 to 18 °C was a result of a temperature influence on production of leaf area rather than the effect of photosynthesis per unit of leaf. Net assimilation rates decreased with increase in temperature at all light intensities.

EAR LENGTH AND SPIKELET NUMBER OF WHEAT GROWN AT DIFFERENT TEMPERATURES AND LIGHT INTENSITIES

1965 ◽  
Vol 43 (3) ◽  
pp. 345-353 ◽  
Author(s):  
D. J. C. Friend
Keyword(s):  
Light Intensity ◽  
Low Temperatures ◽  
Dry Weight ◽  
High Light ◽  
Morphological Development ◽  
Spikelet Number ◽  
Light Intensities ◽  
Different Temperatures ◽  
Total Plant ◽  
Effects Of Temperature

The number of spikelets on the differentiating inflorescence and the ear at anthesis was highest at high light intensities and at low temperatures. The length of the developing inflorescence and the ear, the height of the main stem, and the total plant dry weight at the time of anthesis were also greatest under these conditions.These results are related to differential effects of temperature and light intensity on the rates and duration of apical elongation, morphological development of the ear, and spikelet formation.

Influence of temperature on net CO2 exchange in roses

1991 ◽  
Vol 71 (1) ◽  
pp. 235-243 ◽  
Author(s):  
J. Jiao ◽  
M. J. Tsujita ◽  
B. Grodzinski
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Effect Of Temperature ◽  
Flower Bud ◽  
Temperature Range ◽  
Whole Plant ◽  
Optimal Temperature Range ◽  
Influence Of Temperature On ◽  
Whole Plants

The effect of temperature on net CO2 exchange of source and sink tissues of the flowering shoots and of whole plants was examined using single-stemmed Samantha roses. At all stages of shoot development, the optimal temperature range for whole-plant carbon (C) gain at saturating irradiance and ambient CO2 level was between 20° and 25 °C, narrower than the temperature range for optimal leaf net photosynthesis. Dark respiration increased more dramatically than photosynthesis with temperatures between 15 and 35 °C. At 25 °C, C loss due to respiration from the flower bud at colour bud stage accounted for 45% of the C loss of the flowering shoot. At low irradiance levels (e.g. 200 μmol m−2 s−1) whole-plant net photosynthesis was greater at 16° than at 22 °C because of a greater reduction in respiration. Lowering the night temperature from 27 to 17 °C also increased daily C gain due to a reduction in the C lost at night. Whole-plant net photosynthesis of plants grown and measured at enriched (1000 ± 100 μL L−1) CO2 was greater than that of plants grown and measured at ambient (350 ± 50 μL L−1) level at temperatures between 15° and 35 °C. Furthermore, the optimal temperatures for whole-plant net photosynthesis in CO2 enrichment was higher than at ambient CO2 level. Key words: Dark respiration, net photosynthesis, Rosa hybrida, temperature

The ecology of Ramalina menziesii. VI. Laboratory responses of net CO2 exchange to moisture, temperature, and light

1987 ◽  
Vol 65 (1) ◽  
pp. 182-191 ◽  
Author(s):  
U. Matthes-Sears ◽  
T. H. Nash III ◽  
D. W. Larson
Keyword(s):  
Dark Respiration ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Response Curves ◽  
Central California ◽  
Photosynthetic Rates ◽  
Chlorophyll Contents ◽  
The Mean ◽  
The Difference ◽  
Thallus Water Content

The response of net CO2 exchange to thallus water content, thallus temperature, and photosynthetically active radiation was measured in the laboratory for two morphologically different forms of Ramalina menziesii collected from a coastal and an inland habitat in central California. Equations describing the response curves are fitted to the data and compared statistically for the two sites during two seasons. Significant differences were present for all responses both in summer and winter but were more pronounced for net photosynthesis than for dark respiration. The main differences between the two forms were in the absolute rates of net photosynthesis; a maximum of 6.2 was measured for the inland form but only 3.6 mg∙g−1∙h−1 for the coastal form. Chlorophyll contents were also different between the two forms, indicating that chlorophyll is the likely cause for the difference in net photosynthetic rates. Net photosynthetic rates were higher at low temperatures during winter than during summer, but otherwise seasonal variations in the gas exchange responses were relatively minor. Both forms of the lichen are light saturated at quantum fluxes greater than 200 μE∙m−2∙s−1. Both show an optimum temperature for maximum CO2 exchange at 25 °C, well above the mean operating temperature of R. menziesii in the field.

scholarly journals Photosynthetic responses of three common mosses from continental Antarctica

2005 ◽  
Vol 17 (3) ◽  
pp. 341-352 ◽  
Author(s):  
STEFAN PANNEWITZ ◽  
T.G. ALLAN GREEN ◽  
KADMIEL MAYSEK ◽  
MARK SCHLENSOG ◽  
ROD SEPPELT ◽  
...  
Keyword(s):  
Climate Change ◽  
Water Content ◽  
Dark Respiration ◽  
Temperature Response ◽  
Environmental Parameters ◽  
Net Photosynthesis ◽  
Photon Flux ◽  
Terrestrial Vegetation ◽  
Moss Species ◽  
Victoria Land

Predicting the effects of climate change on Antarctic terrestrial vegetation requires a better knowledge of the ecophysiology of common moss species. In this paper we provide a comprehensive matrix for photosynthesis and major environmental parameters for three dominant Antarctic moss species (Bryum subrotundifolium, B. pseudotriquetrum and Ceratodon purpureus). Using locations in southern Victoria Land, (Granite Harbour, 77°S) and northern Victoria Land (Cape Hallett, 72°S) we determined the responses of net photosynthesis and dark respiration to thallus water content, thallus temperature, photosynthetic photon flux densities and CO2 concentration over several summer seasons. The studies also included microclimate recordings at all sites where the research was carried out in field laboratories. Plant temperature was influenced predominantly by the water regime at the site with dry mosses being warmer. Optimal temperatures for net photosynthesis were 13.7°C, 12.0°C and 6.6°C for B. subrotundifolium, B. pseudotriquetrum and C. purpureus, respectively and fall within the known range for Antarctic mosses. Maximal net photosynthesis at 10°C ranked as B. subrotundifolium > B. pseudotriquetrum > C. purpureus. Net photosynthesis was strongly depressed at subzero temperatures but was substantial at 0°C. Net photosynthesis of the mosses was not saturated by light at optimal water content and thallus temperature. Response of net photosynthesis to increase in water content was as expected for mosses although B. subrotundifolium showed a large depression (60%) at the highest hydrations. Net photosynthesis of both B. subrotundifolium and B. pseudotriquetrum showed a large response to increase in CO2 concentration and this rose with increase in temperature; saturation was not reached for B. pseudotriquetrum at 20°C. There was a high level of variability for species at the same sites in different years and between different locations. This was substantial enough to make prediction of the effects of climate change very difficult at the moment.

scholarly journals PHOTOSYNTHESIS, RESPIRATION, AND CARBON COST OF DEVELOPING RABBITEYE BLUEBERRY FRUIT

HortScience ◽  
1990 ◽  
Vol 25 (9) ◽  
pp. 1165g-1166
Author(s):  
Keith Birkhold ◽  
Rebecca Darnell ◽  
Karen Koch
Keyword(s):  
Weight Gain ◽  
Fruit Development ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Total Carbon ◽  
Vaccinium Ashei ◽  
Gross Photosynthesis ◽  
Carbon Cost ◽  
Fruit Photosynthesis

Carbon exchange and content of blueberry (Vaccinium ashei) fruit were measured from anthesis through fruit ripening in order to determine the amount of imported carbon required for fruit development. Net photosynthesis occurred in blueberry fruit from petal fall through color break. During this time, gross photosynthesis of fruit decreased from 30.1 μmol CO2·g fw-1·hr-1 to 4.8 μmol CO2·g fw-1·hr-1, and dark respiration decreased from 14.3 μmol CO2·g fw-1·hr-1 to 4.6 μmol CO2·g fw-1·hr-1. After color break, the photosynthetic rate fell to zero, and the respiration rate increased to 8.0 μmol CO2·g fw-1·hr-1, before decreasing. Preliminary data suggest that fruit photosynthesis contributes 11% of the total carbon required (dry weight gain + respiratory loss) during fruit development however, it supplies 50% of the total carbon required during the first 5 days after petal fall. This contribution of carbon from fruit photosynthesis may be critical in initial fruit development since the current season's vegetative growth is not yet providing carbohydrates.

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