Photosynthesis and Respiration of Developing Soybean Pods

1977 ◽  
Vol 4 (5) ◽  
pp. 713 ◽  
Author(s):  
EY Sambo ◽  
J Moorby ◽  
FL Milthorpe
Keyword(s):  
Dark Respiration ◽  
Photochemical Efficiency ◽  
Net Photosynthesis ◽  
Dry Weight ◽  
Daily Basis ◽  
Co2 Uptake ◽  
Response Curves ◽  
Total Import ◽  
Co2 Response ◽  
Gross Photosynthesis

Net CO2 uptake by soybean pods in the light was much less and output in darkness much greater than from equal areas of leaves. The net photosynthesis decreased, becoming negative, and dark respiration increased as seed filling progressed. The photochemical efficiency was the same but the diffusive resistance of pods was about twice and the internal resistance two to three times those of leaves. Fluxes into open deseeded pods were initially much greater than into intact pods but drying out of the tissue soon led to fluxes only about three times greater. From these measurements and light- and CO2-response curves of intact pods, estimates of gross photosynthesis, photorespiration and dark respiration of seeds and hulls were made. These indicated that seed reassimilated slightly more CO2 than they respired when young and about two-thirds thereof at a later stage. Hulls fixed about similar amounts but these were insufficient to prevent net effluxes from pods during the later stages of their development, even at irradiances of 190 W m-2. On a daily basis, direct uptake of CO2 made a negligible contribution to the total import of dry weight by the pod; nevertheless, photosynthesis in the seeds and hulls refixed some 50-70% of the CO2 respired by these tissues.

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.

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.

Temperature Response of Whole-plant CO2 Exchange Rates of Magnolia (Magnolia grandiflora L.)

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 511d-511
Author(s):  
Marc W. van Iersel ◽  
Orville M. Lindstrom
Keyword(s):  
Dark Respiration ◽  
Temperature Response ◽  
Net Photosynthesis ◽  
Co2 Exchange ◽  
Limiting Factor ◽  
Response Curves ◽  
Gross Photosynthesis ◽  
Temperature Range ◽  
Whole Plant ◽  
Increasing Temperature

Photosynthesis and respiration temperature-response curves are useful in predicting the ability of plants to perform under different environmental conditions. Whole crop CO2 exchange of two groups of magnolia `Greenback' plants was measured over a 26 °C temperature range. Net photosynthesis (Pnet) increased from 2 to 17% C and decreased again at higher temperatures. The Q10 for Pnet decreased from ≈4 at 6 °C to 0.5 at 24 °C. The decrease in Pnet at temperatures over 17 °C was caused by a rapid increase in dark respiration (Rdark) with increasing temperature. The Q10 for Rdark was estimated by fitting an exponential curve to data, resulting in a temperature-independent Q10 of 2.8. Gross photosynthesis (Pgross), estimated as the sum of Rdark and Pnet, increased over the entire temperature range (up to 25 °C). The Q10 for Pgross decreased with increasing temperature, but remained higher than 1. The data suggest that high respiration rates may be the limiting factor for growth of magnolia exposed to high temperatures, since it may result in a net carbon loss from the plants. At temperatures below 5 °C, both Pnet and Rdark become low and the net CO2 exchange of the plants would be expected to be minimal.

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.

scholarly journals Short-term Temperature Change Affects the Carbon Exchange Characteristics and Growth of Four Bedding Plant Species

2003 ◽  
Vol 128 (1) ◽  
pp. 100-106 ◽  
Author(s):  
Marc W. van Iersel
Keyword(s):  
Growth Rate ◽  
Dark Respiration ◽  
Net Photosynthesis ◽  
Tagetes Patula ◽  
Short Term ◽  
Response Curves ◽  
Gross Photosynthesis ◽  
Bedding Plants ◽  
Bedding Plant ◽  
Wide Range

Bedding plants are exposed to a wide range of environmental conditions, both during production and in the landscape. This research compared the effect of short-term temperature changes on the CO2 exchange rates of four popular bedding plants species. Net photosynthesis (Pnet) and dark respiration (Rdark) of geranium (Pelargonium ×hortorum L.H. Bail.), marigold (Tagetes patula L.), pansy (Viola ×wittrockiana Gams.), and petunia (Petunia ×hybrida Hort. Vilm.-Andr.) were measured at temperatures ranging from 8 to 38 °C (for Pnet) and 6 to 36 °C (for Rdark). Net photosynthesis of all species was maximal at 14 to 15 °C, while Rdark of all four species increased exponentially with increasing temperature. Gross photosynthesis (Pgross) was estimated as the sum of Pnet and Rdark, and was greater for petunia than for the other three species. Gross photosynthesis was less sensitive to temperature than either Pnet or Rdark, suggesting that temperature effects on Pnet were caused mainly by increased respiration at higher temperatures. Gas exchange-temperature response curves were not useful in determining the heat tolerance of these species. There were significant differences among species in the estimated Rdark at 0 °C and the Q10 for Rdark. Differences in the Q10 for Rdark were related to growth rate and plant size. Large plants had a greater Q10 for Rdark, apparently because these plants had a higher ratio of maintenance to growth respiration than small plants. The Q10 of the maintenance respiration coefficient was estimated from the correlation between the Q10 and relative growth rate, and was found to be 2.5 to 2.6.

The morphological basis of variation in net photosynthetic and respiratory responses of the mat-forming lichen species Stereocaulon virgatum and S. tomentosum

1989 ◽  
Vol 67 (1) ◽  
pp. 167-176 ◽  
Author(s):  
D. S. Coxson ◽  
J. Lancaster
Keyword(s):  
Water Vapor ◽  
Dark Respiration ◽  
Cloud Forest ◽  
A Priori ◽  
Net Photosynthesis ◽  
Vapor Transport ◽  
Water Vapor Transport ◽  
Response Curves ◽  
Morphological Variations ◽  
Closed Canopy

Response patterns of net photosynthesis and dark respiration are examined in two species of Stereocaulon: S. tomentosum Fr., from early successional pine forest communities of the southern Canadian Rockies, and S. virgatum Ach., an early colonizer in tropical cloud-forest environments. These responses, measured in both intact and dissected mat segments, are described in the context of the influence of morphological variations on patterns of water vapor transport. Saturation response curves are fitted to data, allowing description of maximal rates of both net photosynthesis and dark respiration, water contents at which rates are half maximal, maximal water efficiency, and moisture compensation points. In S. tomentosum the closed-canopy nature of the lichen mat profile results in the development of a distinct shade ecotype in lower thallus segments. This canopy profile also impedes water vapor transport from within the mat profile, creating a more mesic microclimate for photobionts located at depth within the lichen mat. This stands in contrast to the open upper canopy profile of S. virgatum, which allows greater convective exchange at depth and appears to preclude the development of distinct sun–shade photobiont ecotypes. Net photosynthetic activity remains high in fully saturated thalli of S. tomentosum, yet in S. virgatum it is depressed by over 50% at full thallus saturation. This greater depression of photosynthetic uptake at full thallus saturation in the species of the more mesic environment contradicts a priori assumptions based on previous concepts of xeric–mesic response gradients in lichens. These responses are discussed in context of other selective pressures influencing lichen mat morphology.

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 Rate, Flowering, and Yield Component Alteration in Hazelnut in Response to Different Light Environments

1996 ◽  
Vol 121 (6) ◽  
pp. 1103-1111 ◽  
Author(s):  
Cheryl R. Hampson ◽  
Anita N. Azarenko ◽  
John R. Potter
Keyword(s):  
Photosynthetic Rate ◽  
Dark Respiration ◽  
Stomatal Density ◽  
Chlorophyll Concentration ◽  
Light Response ◽  
Dry Weight ◽  
Yield Component ◽  
Response Curves ◽  
Photosynthetic Rates ◽  
Light Response Curves

In hazelnut (Corylus avellana L.), vigorous vegetative growth and traditional orchard practices that include little or no pruning combine to produce a dense, shady canopy. A study designed to quantify the effect of shade on reproduction and photosynthetic rate in this shade-tolerant species was undertaken to assess whether some degree of pruning might improve productivity. Shade cloth was used to exclude 30%, 47%, 63%, 73%, or 92% of ambient sunlight from whole `Ennis' and `Barcelona' trees from mid-May until harvest. Photosynthetic light response curves were obtained for leaves that had developed in full sunlight, deep inside the canopy of unshaded trees, or in 92% shade. Light-saturated net photosynthetic rates were 12.0, 6.1, and 9.3 μmol·m-2·s-1 of CO2 and dark respiration rates were 2.0, 1.1, and 0.7 μmol·m-2·s-1 of CO2, respectively, for the three light regimes. Light-saturated photosynthetic rates of leaves from 30% or 63% shade differed little from the control (0% shade). Area per leaf increased by 49% and chlorophyll concentration (dry weight basis) by 157% as shading increased from 0% to 92%. Shading to 92% reduced specific leaf weight (68%), stomatal density (30%), light compensation point (69%), and dark respiration rate (63%) compared to controls. Female inflorescence density declined by about one-third and male inflorescence density by 64% to 74% in the most heavily shaded trees of both cultivars compared to controls. Shade was more detrimental to yield than flowering: yield per tree dropped by >80%, from 2.9 to 3.4 kg in full sun to 0.6 to 0.9 kg in 92% shade. Shade reduced yield primarily by decreasing nut number and secondarily by decreasing nut size. The incidence of several kernel defects increased as shade increased. Therefore, hazelnut leaves showed considerable capacity to adapt structurally and functionally to shade, but improving light penetration into the canopy would probably increase orchard productivity.

scholarly journals Shading Affects Morphology, Dry-matter Partitioning, and Photosynthetic Response of Greenhouse-grown `Chardonnay' Grapevines

HortScience ◽  
2004 ◽  
Vol 39 (1) ◽  
pp. 65-70 ◽  
Author(s):  
Justine E. Vanden Heuvel ◽  
John T.A. Proctor ◽  
K. Helen Fisher ◽  
J. Alan Sullivan
Keyword(s):  
Dry Matter ◽  
Dark Respiration ◽  
Light Response ◽  
Leaf Size ◽  
Dry Weight ◽  
Volume Density ◽  
Response Curves ◽  
Dry Matter Partitioning ◽  
Light Response Curves ◽  
Whole Plant

In order to gain an understanding of the capacity of severely shaded leaves to be productive in dense canopies, the effects of increased shading on morphology, dry-matter partitioning, and whole-plant net carbon exchange rate (NCER) were investigated on greenhouse-grown Vitis vinifera L. `Chardonnay' grapevines. Vines were subjected to whole-plant shading levels of 0%, 54%, 90%, and 99% of direct sun 3 weeks after potting. Data were collected 8 to 10 weeks after potting. Nonlinear regression was used to investigate the relationship of leaf morphological traits and organ dry weights to increased shading. Leaf size was maintained with increased shading to approximately the 90% shading level, while leaf fresh weight, volume, density, and thickness were immediately reduced with increased shading. Root dry weight was most affected by increased shading, and root to shoot ratio was reduced. When nonlinear regressions were produced for light response curves, light compensation point was reduced by approximately 49% by moderate shading, and 61% by severe shading. Shaded leaves approached the asymptote of the light response curve more quickly, and had reduced dark respiration rates, indicating that the morphological compensation responses by the vine allow shaded leaves to use available light more efficiently. However, the long-term ramifications of reduced root growth in the current year on vines with shaded leaves may be significant.

Photosynthetic light and temperature responses of Eucalyptus cloeziana and Eucalyptus argophloia

2003 ◽  
Vol 51 (5) ◽  
pp. 573 ◽  
Author(s):  
Michael R. Ngugi ◽  
Mark A. Hunt ◽  
David Doley ◽  
Paul Ryan ◽  
Peter J. Dart
Keyword(s):  
Quantum Yield ◽  
Dark Respiration ◽  
Temperature Response ◽  
Net Photosynthesis ◽  
Photosynthetic Photon Flux Density ◽  
Photon Flux ◽  
Photon Flux Density ◽  
Response Curves ◽  
Growth Environment ◽  
Eucalyptus Cloeziana

Acclimation of gas exchange to temperature and light was determined in 18-month-old plants of humid coastal (Gympie) and dry inland (Hungry Hills) provenances of Eucalyptus cloeziana F.Muell., and in those of a dry inland provenance of Eucalyptus argophloia Blakely. Plants were acclimated at day/night temperatures of 18/13, 23/18, 28/23 and 33/28�C in controlled-temperature glasshouses for 4 months. Light and temperature response curves were measured at the beginning and end of the acclimation period. There were no significant differences in the shape and quantum-yield parameters among provenances at 23, 28 and 33�C day temperatures. Quantum yield [μmol CO2 μmol–1 photosynthetic photon flux density (PPFD)] ranged from 0.04 to 0.06 and the light response shape parameter ranged from 0.53 to 0.78. Similarly, no consistent trends in the rate of dark respiration for plants of each provenance were identified at the four growth temperatures. Average values of dark respiration for the plants of the three provenances ranged from 0.61 to 1.86 μmol m–2 s–1. The optimum temperatures for net photosynthesis increased from 23 to 32�C for the humid- and from 25 to 33�C for the dry-provenance E. cloeziana and from 21 to 33�C for E. argophloia as daytime temperature of the growth environment increased from 18 to 33�C. These results have implications in predicting survival and productivity of E. cloeziana and E. argophloia in areas outside their natural distribution.

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