141 POSTER SESSION 23 Nutrition & Photosynthesis/Fruits (General)
David C. Percival, John T.A. Proctor, and M.J. Tsujita
M. Raviv, J.H. Lieth, and D.W. Burger
Rose plants (cv. Kardinal, grafted on Natal Brier) were grown in UC mix (42% fir bark, 33% peat, and 25% sand) and in coir. Water tension in the media was maintained within a predetermined narrow range using electronic tensiometers. Whole plant net photosynthesis as a function of the water tension in the medium was determined and the results were later normalized to measured leaf area. Simultaneous measurements of metabolic heat and respiration rate were carried out on detached young (FW = 10-20 mg.) leaflet samples, using differential scanning calorimeter (model 4100, Calorimetry Sciences, Provo, Utah). Only a small amount of plant material is removed for analyses so the assay is essentially non-destructive for the whole plant. Physical characteristics of the media greatly affect the relationship between water tension and water availability to plants. At similar tension values, water availability is much lower in coir than in UC mix. The effects of water availability on net photosynthesis, metabolic heat rate, and respiration will be discussed in relation to their effect on productivity.
E.D. Leonardos, M.J. Tsujita, B. Grodzinski, and T.J. Blom
Leaf and whole plant gas exchange (net photosynthesis Pn, dark respiration Dr, transpiration Tr, and resistance R) of `Jacqueline' Alstroemeria, grown in pots inside a greenhouse, were measured under lab conditions using an openflow and a semi-closed system respectively.
Temperature responses of apical fully expanded leaves, on flowering and non-flowering shoots, showed an optimum range for net photosynthesis (Pn) from 15 to 20 °C. Above 25 °C Pn dropped considerably as temperature increased. Leaf transpiration rates over the same range of temperature showed a similar decrease, indicating that low leaf Pn rates at higher temperatures were due in part to increased stomatal resistance.
Whole plant photosynthetic response to temperature was similar to that of leaf gas exchange. The optimum temperature range for whole plant Pn was from 12 to 17 °C. These results show that moderately low temperatures are essential for carbon assimilation and efficient water use in Alstroemeria. Temperature interactions with other environmental factors will also be presented in models describing Pn rates as a function of irradiance, CO2 concentration, and temperature.
Jason J. Griffin, Thomas G. Ranney, and D. Mason Pharr
Net photosynthesis (Pn) of two ecotypes of redbud (Cercis canadensis L.) was studied following growth under high temperatures and increasing drought. Although mexican redbud [C. canadensis var. mexicana (Rose) M. Hopkins] exhibited greater Pn than eastern redbud (C. canadensis var. canadensis L.), Pn decreased at a similar rate under water deficit stress for both ecotypes. Mexican redbud also had greater instantaneous water use efficiency [net photosynthesis: transpiration (WUE)] than eastern redbud. Differences in both Pn and WUE might have been due to differences in leaf thickness. The optimum temperature for potential photosynthetic capacity (37 °C) was unaffected by irrigation or ecotype. Tissue osmotic potential at full turgor was more negative in eastern redbud, but was unaffected by drought stress in either ecotype. Soluble carbohydrate content was higher in eastern redbud, and in both ecotypes, d-pinitol was the major soluble carbohydrate and was considerably more abundant in the water-stressed plants. Total polyol content (myo-inositol + ononitol + pinitol) was also greater in the water-stressed plants. Both ecotypes were very tolerant of high temperatures and drought.
Susanna Marchi, Luca Sebastiani, Riccardo Gucci, and Roberto Tognetti
Net photosynthesis, dark respiration, chlorophyll and carbohydrate content, and leaf and shoot growth of deciduous peach [Prunus persica (L.) Batsch] saplings, grown in greenhouse conditions, were measured to assess changes in carbon balance during leaf development. The 6th, 12th, and 16th leaf node were measured from the first flush at the base through expansion to maturity (the first node being the oldest). Shoot and leaves expanded following a sigmoid pattern in all nodes. The shape of the logistic curve did not vary between the 6th and the 16th leaf node, while the 12th leaf node showed a steeper response, suggesting that the latter reached 50% expansion relatively earlier. Photosynthesis varied with leaf development as young leaves had low CO2 assimilation rates that were reflected in their chlorophyll concentration. Net daily CO2 assimilation was negative in young expanding leaves. The sink-source transition, defined to be the time when the increase in daily carbohydrate exchange rate exceeded the daily increase in leaf carbohydrate content, occurred before full leaf expansion. The transition from import to export was attained 11-12 days after budbreak (corresponding to 41% to 45% of full leaf expansion) for the 6th leaf, about 7-9 days after (38% to 52% of full expansion) for the 12th leaf and after 9-10 days (32% to 38% of full expansion) for the 16th leaf. Below 30% to 50% of full expansion leaves might not respond to assimilate requirements from sinks, being sinks themselves.
Rongcai Yuan and Duane W. Greene
BA was applied at 50 or 100 mg·L-1 to `More-Spur McIntosh'/Malling 7 (M.7) apple trees [Malus sylvestris (L.) Mill var. domestica (Borkh.) Mansf.] at the 10 mm stage of fruit development. BA thinned fruit and increased fruit size. There were two distinguishable peaks of fruit abscission during `June drop'. BA accentuated the naturally occurring waves of fruit abscission, and enhanced translocation of 14C-sorbitol from leaves to fruit when applied directly to the fruit, but not when applied directly to the leaves. Net photosynthesis was decreased and dark respiration was increased when temperature following BA application was high (30 °C), whereas there was no effect when temperature was lower (20 °C). Total nonstructural carbohydrates, total soluble sugars, and starch in the leaves decreased dramatically over the 12- or 13-day observation period, regardless of BA treatment. These carbohydrate concentrations in the leaves were lowered further by BA application. Abscising fruit, based on specific reddening of the pedicel, had higher carbohydrate levels than persisting fruit, regardless of BA application. We conclude that BA thins fruit, at least in part, by increasing dark respiration and decreasing net photosynthesis. Chemical name used: N-(phenylmethyl)-1H-purine-6-amine [benzyladenine (BA)].
Jens N. Wünsche, Alan N. Lakso, Terence L Robinson, Fritz Lenz, and Steven S. Denning
Although apple (Malus domestica Borkh.) system yield differences are generally related to whole-canopy light interception, this study tested the hypothesis that these orchard yields are related primarily to total light intercepted by the spur canopy. Seasonal leaf area development of different shoot types, exposed bourse shoot leaf net photosynthesis, fruit growth, whole canopy light interception (by image analysis of fisheye photographs) and relative light interception by different shoot types (by a laser assisted canopy scanning device) were estimated within four 14-year-old `Empire' apple production systems (slender spindle/M.9, central leader/M.7, central leader/M.9/MM.111 and Y-trellis/M.26). The final LAI values were CL/M.7 = 1.8, CL/9/111 = 2.3, SS/M.9 = 2.6 and Y/M.26 = 3.6. Exposed leaf net photosynthesis showed few differences and was not dependent upon the production system. Yields of the pyramidal shaped tree forms were 40 to 42 t·ha-1 while Y-trellis produced 59 t·ha-1, with similar fruit sizes. Again, yields were primarily related to the percentage of light intercepted by the whole canopy, 48% to 53% for conic forms versus 62% for the Y-trellis system. Laser analyses showed that the Y-trellis system intercepted about 20% to 30% more light with the spur canopy than the conic tree forms, supporting the hypothesis. Yields were better correlated with spur canopy LAI and spur canopy light interception than with extension shoot canopy LAI and light interception.
Ian R. Rodriguez, Lambert B. McCarty, Joe E. Toler, and Roy B. Dodd
Use of creeping bentgrass [Agrostis stoloniferous L. var. palustris (Huds.)] on golf greens has expanded into the hotter, more humid regions of the United States where its quality is often low during summer months. The summer decline in bentgrass quality may be partially attributed to respiration rates exceeding photosynthesis during periods of supraoptimal temperatures and adverse soil conditions, such as excessive CO2 and inadequate O2 levels. The objectives of this study were to examine the effects of high temperature, high soil CO2, and irrigation scheduling on creeping bentgrass growth. A growth chamber study was conducted using `A-1' creeping bentgrass. Treatments included all combinations of three day/night temperature regimes (26.5/21 °C, 29.5/24 °C, and 32/26.5 °C), three irrigation schedules (field capacity daily, field capacity every two d, and half field capacity daily), and four soil CO2 injection levels (10%, 5%, 0.03%, and a noinjection control). Creeping bentgrass shoot and root dry weights and net photosynthetic rates were greater for day/night temperatures <32/26.5 °C. High temperatures (32/26.5 °C) and 10% CO2 reduced bentgrass net photosynthesis by 37.5 μmol CO2/m2/s. Shoot and root total nonstructural carbohydrates also were lowest for highest temperature regime. Respiration exceeded gross photosynthesis at 32/26.5 °C when 5% and 10% CO2 injection levels were used, indicating a carbon deficit occurred for these conditions. Irrigation volume and frequency did not affect bentgrass growth. High temperatures combined with high soil CO2 levels produced poorest turf quality.
Jun Ying Zhao, Li Jun Wang, Pei Ge Fan, Zhan Wu Dai, and Shao Hua Li
Half or whole root systems of micropropagated `Gala' apple (Malus ×domestica Borkh.) plants were subjected to drought stress by regulating the osmotic potential of the nutrient solution using polyethylene glycol (20% w/v) to investigate the effect of root drying on NO3- content and metabolism in roots and leaves and on leaf photosynthesis. No significant difference in predawn leaf water potential was found between half root stress (HRS) and control (CK), while predawn leaf water potential from both was significantly higher than for the whole root stress (WRS) treatment. However, diurnal leaf water potential of HRS was lower than CK and higher than WRS during most of the daytime. Neither HRS nor WRS influenced foliar NO3- concentration, but both significantly reduced NO3- concentration in drought-stressed roots as early as 4 hours after stress treatment started. This reduced NO3- concentration was maintained in HRS and WRS roots to the end of the experiment. However, there were no significant differences in NO3- concerntation between CK roots and unstressed roots of HRS. Similar to the effect on root NO3- concentration, both HRS and WRS reduced nitrate reductase activity in drought-stressed roots. Moreover, leaf net photosynthesis, stomatal conductance and transpiration rate of HRS plants were reduced significantly throughout the experiment when compared with CK plants, but the values were higher than those of WRS plants in the first 7 days of stress treatment though not at later times. Net photosynthesis, stomatal conductance and transpiration rate were correlated to root NO3- concentration. This correlation may simply reflect the fact that water stress affected both NO3- concentration in roots and leaf gas exchange in the same direction.
Jonathan M. Frantz and Bruce Bugbee
Cloudy days cause an abrupt reduction in daily photosynthetic photon flux (PPF), but we have a poor understanding of how plants acclimate to this change. We used a unique 10-chamber, steady-state, gas-exchange system to continuously measure daily photosynthesis and night respiration of populations of a starch accumulator [tomato (Lycopersicon esculentum Mill. cv. Micro-Tina)] and a sucrose accumulator [lettuce (Lactuca sativa L. cv. Grand Rapids)] over 42 days. All measurements were done at elevated CO2 (1200 μmol·mol-1) to avoid any CO2 limitations and included both shoots and roots. We integrated photosynthesis and respiration measurements separately to determine daily net carbon gain and carbon use efficiency (CUE) as the ratio of daily net C gain to total day-time C fixed over the 42-day period. After 16 to 20 days of growth in constant PPF, plants in some chambers were subjected to an abrupt PPF reduction to simulate shade or a series of cloudy days. The immediate effect and the long term acclimation rate were assessed from canopy quantum yield and carbon use efficiency. The effect of shade on carbon use efficiency and acclimation was much slower than predicted by widely used growth models. It took 12 days for tomato populations to recover their original CUE and lettuce CUE never completely acclimated. Tomatoes, the starch accumulator, acclimated to low light more rapidly than lettuce, the sucrose accumulator. Plant growth models should be modified to include the photosynthesis/respiration imbalance and resulting inefficiency of carbon gain associated with changing PPF conditions on cloudy days.