On Photosynthesis and Organic Carbon, Carbon Dioxide, and Oxygen Flows in the Ocean

The modern concept of photosynthesis as a mechanism for utilizing the energy of solar radiation is used as the basis for assessing the scale of photosynthetic production of initial organic matter in the ocean (primary biological production), its destruction, the carbon and carbon dioxide cycles (flows) involved in this process, and the size of oil- and gas-bearing hydrocarbonaceous formations originating in sedimentary deposits.     

Effect of Temperature, CO(2) Concentration, and Light Intensity on Oxygen Inhibition of Photosynthesis in Wheat Leaves

The effect of 21% O₂ and 3% O₂ on the CO₂ exchange of detached wheat leaves was measured in a closed system with an infrared carbon dioxide analyzer. Temperature was varied between 2° and 43°, CO₂ concentration between 0.000% and 0.050% and light intensity between 40 ft-c and 1000 ft-c. In most conditions, the apparent rate of photosynthesis was inhibited in 21% O₂ compared to 3% O₂. The degree of inhibition increased with increasing temperature and decreasing CO₂ concentration. Light intensity did not alter the effect of O₂ except at light intensities or CO₂ concentrations near the compensation point. At high CO₂ concentrations and low temperature, O₂ inhibition of apparent photosynthesis was absent. At 3% O₂, wheat resembled tropical grasses in possessing a high rate of photosynthesis, a temperature optimum for photosynthesis above 30°, and a CO₂ compensation point of less than 0.0005% CO₂. The effect of O₂ on apparent photosynthesis could be ascribed to a combination of stimulation of CO₂ production during photosynthesis, and inhibition of photosynthesis itself.     

Effects of Strong Light and Active Oxygen on Photosynthesis in Soybean

With the use of chlorophyll fluorescence technique, it was found that the net photosynthetic oxygen evolution rate decreased after strong light (2 000 μmol· m-2·2-1 ) treatment for two hours in soybean ( Glycine max L. ) leaves. The chlorophyll fluorescence parameters, Fm/Fo, Fv/Fm, ФPSII, qp and qN decreased along with the increase of light intensity. In strong light, exogenous active oxygen H202、·OH and 'O2 were harmful to soybean leaves. The destruction of 'O2 and·OH to leaves was most evident, as was shown that Fv/Fm and PS H decreased significantly. The antioxidants DABCO, mannitol, ascorbate and histidine protected the leaves, but weakly, from strong light. In darkness, the SOD inhibitor sodium diethyldithiocar- bamate (DDC) had no significant effect on Fm/Fo and Fv/Fm, but NAN,, the ascorbate peroxidase (APX)inhibitor, significantly decreased Fm/Fo, Fv/Fm and ФPS II. In strong light, however, beth DDC and NaN3 reduced the above-mentioned fluorescence parameters, but NaN3 was more effective than DDC. The results suggested that photoinhibition did take place in soybean leaves under strong light, and it was related to active oxygen in vivo.     

Effects of High Air and Soil Temperature Stress on Growth and Tuberization in Solanum tuberosum

Potato plants (Solanum tuberosum L.) were grown at differentair and soil temperatures to determine the effects of high-temperaturestress on root, tuber, and shoot growth. Cooling the soil (17–27C) at high air temperatures (30–40 C) relieved noneof the visible symptoms of heat stress on shoot growth; norwas the degree of induction to tuberize in leaves increased,as reflected in tuberization of leaf-bud cuttings. Heating thesoil (27–35 C) at cool (17–27 C) air temperatureshad no apparent detrimental effect on shoot growth or inductionof leaves to tuberize. However, in each case hot soil largelyeliminated tuber development. In one experiment stolons grewup out of the hot soil and formed aerial tubers upon reachingthe cool air. When leaf-bud cuttings from induced plants wereused as a model system, high soil temperatures inhibited tuberdevelopment from the buried leaf buds, in the absence of anyroot growth. Apparently the induction of leaves to tuberizeis affected principally by air rather than soil temperature,but expression of the signal to tuberize can be blocked by highsoil temperature. Solanum tuberosum L., potato, temperature stress, soil temperature, tuberization     

Modelling and Measuring Transpiration from Scots Pine with Increased Temperature and Carbon Dioxide Enrichment

Starting in 1996, individual trees of Scots pine (Pinus sylvestrisL.) aged 30 years, were grown in closed-top chambers and exposedto either normal ambient conditions (CON), elevated CO₂(approx.700 µmol mol^-1; Elev. C), elevated temperature (approx.2 °C and approx. 6 °C above the outside ambient temperatureduring the ‘growing season’ and ‘off season’,respectively; Elev. T) or a combination of elevated CO₂and warmertemperature (Elev. CT). Sap flow was monitored simultaneouslyby the constant-power heat balance method in a total of 16 trees,four for each treatment, over a 32 d period in summer 1998 (afterthe completion of needle expansion and branch elongation). Toquantify the contributions of crown and physical environmentalvariables to total crown transpiration, a ‘sun/shade model’was developed and used to partition the changes in transpirationto different sources. The results of the sap flow measurementsindicate that (1) total daily sap flow (E_tree.d) varied from0.15–3.41 kg per tree; (2) the treatment effect on E_tree.ddependedgreatly on the weather conditions; (3) the cumulative E_tree.dforthe 32 d dropped significantly by 22% relative to CON (P =0.038)under Elev. C and increased significantly by 21% (P =0.043)and 16% (P =0.048) under Elev. T and Elev. CT, respectively.In general, the modelled transpiration gave good agreement withthe sap flow results. The model computations showed that, ona typical sunny day in summer, the effect of treatment on crownstomatal conductance was responsible for approx. 80% of thechange inE_tree.d , while the increase in needle area and theeffect on total radiation absorption contributed only a smallpercentage. Furthermore, sunlit needles were responsible forover 60% of change in transpiration. The effect of the treatmentson E_tree.dwas larger at high temperature and vapour pressuredeficit but was not sensitive to incident daily radiation. Copyright2000 Annals of Botany Company Transpiration model, sap flow, CO₂and temperature elevation, environment-controlled chamber, Pinus sylvestris L.     

The Relationship Between Photosynthesis and Tuber Growth in Solanum tuberosum L.

Measurements of the rate of photosynthesis of plants of Solanumtuberosum L. var. King Edward were made, using ¹⁴CO₂, at weeklyintervals throughout their growth in a controlled environment.Leaf area and dry weight of sections of the plant were alsodetermined. The results are discussed in relation to existingtheories that photosynthesis can be limited by carbohydrateaccumulation in the leaves, and stimulated by the initiationof tubers.     

Effect of Leaf Age and Shading on Photosynthesis in Potatoes (Solanum tuberosum)

The effects of leaf age and of shading on photosynthetic rateand on other leaf parameters of potato (Solanum tuberosum L.)were studied using a portable gas exchange system. A rapid decreasein the rate of photosynthesis during leaf senescence was observed.This was accompanied by an increase in stomatal resistance,and as a result a fairly constant level of sub-stomatal CO₂concentration was maintained at all leaf ages. The reductionin the photosynthetic rate in older leaves was therefore assumedto be essentially mesophyllic in origin, whereas the stomatalresponse was probably secondary. Canopy density significantly affected the rate of photosyntheticreduction with leaf age. Leaves maintained under high radiationintensities manifested a slower decline in their photosyntheticrate, especially in the early stages of their senescence, thanleaves kept under shade conditions. The latter leaves were foundto be more adapted to low radiation intensities, as indicatedby changes in their chlorophyll a:b ratio and specific leafweight Solanum tuberosum L, potato, photosynthetic rate, mesophyll, stomata, leaf age, radiation intensity, chlorophyll a:b ratio     

Effect of Night Temperature on Photosynthesis, Transpiration, and Growth of Spray Carnations

Spray carnation plants were grown for several weeks under an8 h day/16 h night regime at temperatures of approximately 21°C by day and 6, 17, or 30 °C by night. Subsequently,the rates of photosynthesis and transpiration at 20 °C weresimilar. This contrasts with evidence published for some otherspecies. Night temperature had only a slight effect on the plant's growthrate. Leaf area ratios were also similar between treatmentsand for two intervals covering a 5 week period. At the highnight temperature flowers were initiated sooner and there werefewer side shoots per plant than at the lower temperatures. The implications of these results for the optimization of theclimatic environment are discussed briefly, and the resultsare compared with those reported for other species.     

Daily Irradiance and Feedback Inhibition of Photosynthesis at Elevated Carbon Dioxide Concentration in Brassica oleracea

The fundamental cause of down-regulation of photosynthesis at elevated carbon dioxide concentration (EC) is thought to be a slower rate of utilization of saccharides than their stimulated rate of production, but there are few studies directly supporting this idea under field conditions. We hypothesized that within Brassica oleracea, down-regulation would not occur in kohlrabi because it has a large sink for saccharides in an enlarged stem, but would occur in collards, which lack this sink. Field tests were consistent with this hypothesis. In collards, the degree of down-regulation of photosynthesis in plants grown at EC varied depending on the daily integral of photosynthetically active radiation (PAR) of the day prior to the measurement of photosynthetic capacity, as did leaf saccharide content. However, EC did not result in lower leaf contents of chlorophyll, soluble protein, ribulose-1,5-bisphosphate carboxylase, or nitrate in collards, nor was there any evidence of a triose phosphate utilization rate limiting photosynthesis. Experiments in controlled environment chambers confirmed that there was a threshold response for the down-regulation of photosynthesis in collards at EC to the PAR of the previous day, with down-regulation only occurring above a minimum daily integral of PAR. Down-regulation of photosynthesis could be induced in plants grown at ambient carbon dioxide by a single night at low temperature or by a single day with high PAR and EC. In the controlled environment study, the degree of down-regulation of photosynthesis was highly correlated with leaf glucose, fructose, and sucrose contents, and less well correlated with starch content. Hence down-regulation of photosynthesis at EC in collards in the field represented feedback inhibition from the accumulation of soluble saccharides and day-to-day variation in its occurrence was predictable from the weather.     

Carbon Dioxide and Light Responses of Photosynthesis in Cowpea and Pigeonpea during Water Deficit and Recovery

Greenhouse-grown pigeonpea (Cajanus cajan, [L.] Millsp.; cultivar UW-10) and cowpea (Vigna unguiculata, [L.] Walp.; cultivar California No. 5) were well-watered (control) or subjected to low water potential by withholding water to compare their modes of adaptation to water-limited conditions. Leaf CO₂ exchange rate (CER), leaf diffusive conductance to CO₂ (g_l), and CO₂ concentration in the leaf intercellular air space (C_i) were determined at various CO₂ concentrations and photon flux densities (PFD) of photosynthetically active radiation (400 to 700 nanometer). In cowpea, g_l declined to less than 15% of controls and total water potential (ψ_w) at midafternoon declined to −0.8 megapascal after 5 days of withholding water, whereas g_l in pigeonpea was about 40% of controls even though midafternoon ψ_w was −1.9 megapascal. After 8 days of withholding water, ψ_w at midafternoon declined to −0.9 and −2.4 megapascals in cowpea and pigeonpea, respectively. The solute component of water potential (ψ_s) decreased substantially less in cowpea than pigeonpea. Photosynthetic CER at saturation photon flux density (PFD) and ambient external CO₂ concentration (360 microliters per liter) on day 5 of withholding decreased by 83 and 55% in cowpea and pigeonpea, respectively. When measured at external, CO₂ concentration in bulk air of 360 microliters per liter, the CER of cowpea had fully recovered to control levels 3 days after rewatering; however, at 970 microliters per liter the PFD-saturated CERs of both species were substantially lower than in controls, indicating residual impairment. In stressed plants of both species the CER responses to C_i from 250 to 600 microliters per liter indicated that a substantial nonstomatal inhibition of CER had occurred. Although the sensitivity of g_l to water limitation in cowpea suggested a dehydration avoidance response, parallel measurements of CER at various C_i and PFD indicated that photosynthetic activity of cowpea mesophyll was substantially inhibited by the water-limited treatment.     

The Effects of Increased Atmospheric Carbon Dioxide on Growth, Carbohydrates, and Photosynthesis in Radish, Raphanus sativus

The effects of sink capacity on the regulation of the acclimationof photosynthetic capacity to elevated levels of carbon dioxideare important from a global perspective. We investigated theeffeocts of elevated (750 µmol mol^–1) and ambient(350 µmol mol^–1) atmospheric CO₂ on growth, carbohydratelevels, and photosynthesis in radish seedlings from 15 to 46d after planting. In radish, a major sink is the storage root,and its thickening is initiated early. Elevated CO₂ increasedthe accumulation of dry matter by 111% but had no effect onthe acclimation of the rate of photosynthesis or on the levelsof carbohydrates in leaves at dawn. Elevated CO₂ increased thedry weight in storage roots by 105% by 46 d after planting,apparently enhancing the sink capacity. This enhanced capacityseemed to be responsible for absorption of elevated levels ofphotosynthate and to result in the absence of any over-accumulationof carbohydrates in source leaves and the absence of negativeacclimation of photosynthetic capacity at the elevated levelof CO₂. (Received July 4, 1997; Accepted October 16, 1997)     

Effects of Temperature, Light, Nutrients and Carbon Dioxide on the Strength of the Self-Incompatibility Response in Detached Flowers of Lycopersicon peruvianum

The effects of temperature, light, nutrients and CO₂on the gametophyticself-incompatibility response in a clone of Lycopersicon peruvianumhave been quantified using fluorescence microscopy of stylesquashes prepared from detached flowers held under experimentalconditions for 48 h after self pollination. Self-incompatibilitywas significantly weakened by raising the temperature from 15°C to 22 or 25°C, and by incubating flowers withoutan energy source - i.e. in the dark and/or without externallysupplied sucrose. The sucrose effect was not duplicated by equimolarmannitol or a full mineral nutrient solution plus vitamins.CO₂ applied at 5% in air for 8 h after pollination had no detectableeffect on pollen tube arrest. Observed weakening effects werenot sufficient for use in production of selfed seed. They indicate,however, that self-incompatibility in this clone of L. peruvianumis a temperature-sensitive, energy-dependent process, and supportthe oppositional model of self-incompatibility in which incompatiblepollen tubes are actively inhibited. Lycopersicon, Solanaceae, carbon dioxide, light, nutrients, self-incompatibility, temperature     

Glycolate Excretion and the Oxygen to Carbon Dioxide Net Exchange Ratio during Photosynthesis in Chlamydomonas reinhardtii

Chlamydomonas reinhardtii cells were grown in high (5% v/v) or low (0.03% v/v) CO₂ concentration in air. O₂ evolution, HCO₃⁻ assimilation, and glycolate excretion were measured in response to O₂ and CO₂ concentration. Both low- and high-CO₂-grown cells excrete glycolate. In low-CO₂-grown cells, however, glycolate excretion is observed only at much lower CO₂ concentrations in the medium, as compared with high-CO₂-adapted cells. It is postulated that the activity of the CO₂-concentrating mechanism in low-CO₂-grown cells is responsible for the different dependence of glycolate excretion on external CO₂ concentration in low- versus high-CO₂-adapted cells.     

Carbon Dioxide, Oxygen and Ethylene Effects on Potato Tuber Dormancy Release and Sprout Growth

The possible roles of oxygen and carbon dioxide treatments inthe presence or absence of ethylene on tuber dormancy releasein potato (Solanum tuberosumL.) were examined. Using two gascompositions (I: 60% CO₂–20% O₂–20% N₂and II: 20%CO₂–40% O₂–40% N₂), the phase of tuber dormancyand previous storage temperature were demonstrated to be importantparameters for dormancy release by these gas mixtures. Gas Icaused decreased abscisic acid (ABA) levels within 24 h regardlessof previous storage temperature, although this effect was reversible.Exogenous C₂H₄, an effective dormancy release agent, also causeddecreased ABA levels within 24 h. It also enhanced dormancyrelease and further promoted ABA losses by gas I. Gas II treatmentled to slight reductions in ABA levels that were further decreasedby C₂H₄. Sprout length was modelled successfully by multipleregression analysis in terms of glucose and ABA levels withinthe apical eye tissues of Russet Burbank tubers immediatelyafter, and regardless of, previous gas treatments or storagetemperatures. Solanum tuberosum,potato, abscisic acid, ethylene, carbon dioxide, oxygen, dormancy.     

Affinity of RuBP Carboxylases for Carbon Dioxide and Inhibition of the Enzymes by Oxygen

Ribulose bisphosphate carboxylase (E.C.4.1.1.39) was purifiedfrom leaves of Triticum aestivum, Hordeum vulgare, Spinaceaoleracea, Petroselinum crispum, salad mustard-most likely Brassicanapus, Helianthus annuus, Solanum tuberosum, Beta vulgaris,Lolium perenne, Equisetum arvense, Zea mays, Ginkgo biloba,Pteris aquilina, Salix babylonica, Chamaecyparis lawsonianaand Atrichum undulatum by density gradient centrifugation andgel filtration or by ammonium sulphate fractionation, densitygradient centrifugation, ion-exchange chromatography and gelfiltration. Purified enzymes were freeze-dried and then storedat 0 °C to 4 °C. Portions of each enzyme preparationwere reactivated at 25 °C for 5 h in the presence of 10mM HCO₂ and 20 mM MgCl₂-RuBP carboxylase activities were measuredat four different concentrations of CO₂ at 25 °C and pH8.2 in solutions equilibrated with pure nitrogen or air (21%O₂, 79% N₂). K_m(CO₂), V_max and K₁(O₂) values were computed fromthe results. Significant differences were found in the K_m(CO₂)values for enzymes isolated from different species. Sensitivityof the enzymes to oxygen was less variable.