Physiological acclimation of plants to light has been studied mostly at the leaf level; however whole-plant responses are more relevant in relation to crop growth. To examine the physiological changes associated with different daily light integrals (DLI) during growth of wax begonia (Begonia semperflorens-cultorum Hort.), we grew plants under DLI of 5.3, 9.5, 14.4, and 19.4 mol·m-2·d-1 in a whole-plant gas exchange system. Photosynthesis-light response curves of groups of 12 plants were determined after 25 d of growth. Physiological parameters were estimated per m2 ground area and per m2 leaf area. On a ground area basis, significant increases in dark respiration (Rd), quantum yield (α), the light compensation point (LCP), and maximum gross photosynthesis (Pg,max) were seen with increasing DLI. Variations in physiological parameters among different treatments were small when corrected for differences in leaf area. On a leaf area basis, α, LCP, and the light saturation point (LSP) did not change significantly, whereas significant increases in Rd and Pg,max were seen with increasing DLI. There was a small decrease in leaf chlorophyll concentration (6.3%, measured in SPAD units) with increasing DLI. This study indicates that wax begonias acclimate to low DLI by increasing their leaf chlorophyll concentration, presumably to more efficiently capture the available light, and to high DLI by increasing Pg,max to efficiently utilize the available light, thereby maximizing carbon gain under both situations.
Krishna S. Nemali and Marc W. van Iersel
Sydney Lykins, Katlynn Scammon, Brian T. Lawrence, and Juan Carlos Melgar
photosynthesis ( P Nmax ), dark respiration ( R D ), light compensation point ( I comp ), and light saturation point ( I max ). The P N values at PH or AH did not decline with increasing irradiance, with the exception of the PH curve of ‘Natchez’, which
John Erwin and Esther Gesick
saturation point (irradiance at 95% of P max ), predicted dark respiration rate (CO 2 evolution in dark at 24 °C), and quantum efficiency among three varieties of kale ( Brassica oleracea and B. napus pabularia ), three varieties of spinach ( Spinacea
Elisa Solis-Toapanta and Celina Gómez
is the curvature factor describing the convexity of the curve (range, 0–1). The light compensation point and light saturation point were calculated as the PPF- associated photosynthetic rates when A net = 0 and A net = A max × 0
Gang-Yi Wu, Jun-Ai Hui, Zai-Hua Wang, Jie Li, and Qing-Sheng Ye
CE of RuBPCase. The P n at the CO 2 light saturation point was the regenerating rate of RuBP. Temperature response curve. The P n value of each temperature gradient within the range of 18 to 34 °C was measured from low to high temperature using the
Joshua K. Craver, Krishna S. Nemali, and Roberto G. Lopez
compensation point (LCP), light saturation point (LSP), and quantum yield (α). Measurements were conducted using an LED light source providing a descending PPFD of 1500, 1250, 1000, 500, 250, 100, 50, and 0 µmol·m −2 ·s –1 , with 3 min of acclimation at each
Mengmeng Gu, James A. Robbins, Curt R. Rom, and Hyun-Sug Choi
Net CO2 assimilation (A) of four birch genotypes (Betula nigra L. ‘Cully’, B. papyrifera Marsh., B. alleghaniensis Britton, and B. davurica Pall.) was studied under varied photosynthetic photon flux density (PPFD) and CO2 concentrations (CO2) as indicators to study their shade tolerance and potential for growth enhancement using CO2 enrichment. Effect of water-deficit stress on assimilation under varied PPFD and (CO2) was also investigated for B. papyrifera. The light saturation point at 350 ppm (CO2) for the four genotypes varied from 743 to 1576 μmol·m−2·s−1 photon, and the CO2 saturation point at 1300 μmol·m−2·s−1 photon varied from 767 to 1251 ppm. Light-saturated assimilation ranged from 10.4 μmol·m−2·s−1 in B. alleghaniensis to 13.1 μmol·m−2·s−1 in B. davurica. CO2-saturated A ranged from 18.8 μmol·m−2·s−1 in B. nigra ‘Cully’ to 33.3 μmol·m−2·s−1 in B. davurica. Water-deficit stress significantly reduced the light saturation point to 366 μmol photon m−2·s−1 but increased the CO2 saturation point in B. papyrifera. Carboxylation efficiency was reduced 46% and quantum efficiency was reduced 30% by water-deficit stress in B. papyrifera.
Amanda M. Miller, Marc W. van Iersel, and Allan M. Armitage
Light and temperature responses of whole-plant CO2 exchange were determined for two cultivars of Angelonia angustifolia Benth., `AngelMist Purple Stripe' and `AngelMist Deep Plum'. Whole crop net photosynthesis (Pnet) of `AngelMist Purple Stripe' and `AngelMist Deep Plum' were measured at eight temperatures, ranging from 17 to 42 °C. Pnet for both cultivars increased from 17 to ≈20 °C, and then decreased as temperature increased further. Optimal temperatures for Pnet of `AngelMist Purple Stripe' and `AngelMist Deep Plum' were 20.8 and 19.8 °C, respectively. There was no significant difference between the two cultivars, irrespective of temperature. The Q10 (the relative increase with a 10 °C increase in temperature) for Pnet of both cultivars decreased over the entire temperature range. Dark respiration (Rdark) of both cultivars showed a similar linear increase as temperature increased. As photosynthetic photon flux (PPF) increased from 0 to 600 μmol·m-2·s-1, Pnet of both cultivars increased. Light saturation was not yet reached at 600 μmol·m-2·s-1. The light compensation point occurred at 69 μmol·m-2·s-1 for `AngelMist Purple Stripe' and at 89 μmol·m-2·s-1 for `AngelMist Deep Plum'. The lower light saturation point of `AngelMist Purple Stripe' was the result of a higher quantum yield (0.037 mol·mol-1 for `AngelMist Purple Stripe' and 0.026 mol·mol-1 for `AngelMist Deep Plum'). The difference in quantum yield between the two cultivars may explain the faster growth habit of `AngelMist Purple Stripe'.
Lailiang Cheng, Leslie H. Fuchigami, and Patrick J. Breen
Bench-grafted `Fuji' apple [Malus sylvestris (L.) Mill. var. domestica (Borkh.) Mansf.] trees on Malling 26 (M.26) rootstocks were fertigated for 6 weeks with N concentrations ranging from 0 to 20 mm. These treatments produced levels of leaf N ranging from 0.9 to 4.3 g·m-2. Over this range, leaf absorptance increased curvilinearly from 74.8% to 92.5%. The light saturation point for CO2 assimilation expressed on the basis of absorbed light increased linearly at first with increasing leaf N, then reached a plateau at a leaf N content of ≈3 g·m-2. Under high light conditions (photosynthetic photon flux of 1500 μmol·m-2·s-1), the amount of absorbed light in excess of that required to saturate CO2 assimilation decreased with increasing leaf N. Chlorophyll fluorescence measurements revealed that the maximum photosystem II (PSII) efficiency of dark-adapted leaves was relatively constant over the leaf N range, except for a slight decrease at the lower end. As leaf N increased, nonphotochemical quenching declined under high light, and there was an increase in the efficiency with which the absorbed photons were delivered to open PSII centers. The photochemical quenching coefficient remained high except for a decrease at the lower end of the leaf N range. Actual PSII efficiency increased curvilinearly with increasing leaf N, and was highly correlated with light-saturated CO2 assimilation. The fraction of absorbed light potentially going into singlet oxygen formation was estimated to be ≈10%, regardless of leaf N status. It was concluded that there was more excess absorbed light in low N leaves than in high N leaves under high light conditions. Nonphotochemical quenching was enhanced with decreasing leaf N to reduce both the PSII efficiency and the probability of damage from photooxidation by excess absorbed light.
Jason J. Griffin, Thomas G. Ranney, and D. Mason Pharr
Tolerance to high solar irradiation is an important aspect of stress tolerance for landscape plants, particularly for species native to understory conditions. The objective of this study was to evaluate differential tolerance to high solar irradiation and underlying photosynthetic characteristics of diverse taxa of Illicium L. grown under full sun or 50% shade. Eleven commercially available taxa of Illicium were evaluated for light tolerance by measuring light-saturated photosynthetic capacity (Amax), dark-adapted quantum efficiency of photosystem II (Fv/Fm), and relative chlorophyll content using a SPAD chlorophyll meter. Comparisons of Amax indicated that three of the 11 taxa (I. anisatum L., I. parviflorum Michx. ex Vent., and I. parviflorum `Forest Green') maintained similar rates of light-saturated carbon assimilation when grown in either shade or full sun. All other taxa experienced a significant reduction in Amax when grown in full sun. Chlorophyll fluorescence analysis demonstrated that Fv/Fm was similar between sun and shade plants for the same three taxa that were able to maintain Amax. These taxa appeared to experience less photoinhibition than the others and maintained greater maximum photochemical efficiency of absorbed light. SPAD readings were not significantly reduced in these three taxa either, whereas most other taxa experienced a significant reduction. In fact, SPAD readings were significantly higher in I. parviflorum `Forest Green' when grown under full sun, which also maintained the highest Amax of all the taxa. These results suggest that there is considerable variation in light tolerance among these taxa, with I. parviflorum `Forest Green' demonstrating superior tolerance to high light among the plants compared. A more rigorous examination of I. parviflorum `Forest Green' (high light tolerance) and I. floridanum Ellis (low-light tolerance) demonstrated that I. parviflorum `Forest Green' had a considerably higher Amax, a higher light saturation point, greater potential photosynthetic capacity, reduced susceptibility to photoinhibition as indicated by superior PSII efficiency following light exposure, greater capacity for thermal de-excitation as indicated by a higher rate of nonphotochemical quenching (NPQ) under full sun, greater apparent electron transport rate (ETR) at mid-day, and higher concentrations of the free-radical scavenger myo-inositol. All of these factors contribute potentially to a greater capacity to use light energy for carbon fixation while minimizing photodamage.