leaves, stems, and storage roots in proportion to their growth rates. Bouwkamp (1983) noted that sweetpotato may be source- or sink-limited depending on cultivar, environment, or canopy management. It has been reported that long days enhance vegetative
Victor N. Njiti, Qun Xia, Leonna S. Tyler, Lakeisha D. Stewart, Antione T. Tenner, Chunquan Zhang, Dovi Alipoe, Franklin Chukwuma, and Ming Gao
Yehoshua Saranga, Avishag Levi, Pavel Horcicka, and Shmuel Wolf
The cause for the differences in germination ability of large and small confection sunflower (Helianthus annuus L.) seeds was investigated over 3 years. The source-sink relationship was manipulated to better explore the differences between seeds of various sizes and to study the role of the embryo and the pericarp (hull) in controlling germination ability. Percent germination of large seeds was significantly lower than that of small seeds when tests were performed at 15 °C. Increasing the ratio of leaf area to number of developing seeds caused an increase in mean seed mass, but resulted in a lower percentage of germination. Seed vigor, as measured by mean time to germination or to emergence of hulled seeds or by rate of root elongation, was negatively correlated with embryo mass, indicating that the low vigor of large seeds is not due to the mechanical barrier imposed by the hull. Analysis of electrolyte leakage confirmed the hypothesis that the low quality of large seeds results from a disturbance during the process of seed development.
William B. Miller and Robert W. Langhans
The effects of reduced irradiance on dry weight partitioning in Easter lilies was examined by forcing vernalized bulbs of Lilium longiflorum Thumb. ‘Nellie White’ during two growing seasons. Forcing commenced in a glasshouse under standard growing conditions; immediately following flower bud initiation (FBI), plants were transferred to a range of irradiance reduction treatments (0%, 20%, 50%, or 85% reduction) in the greenhouse or to complete darkness in a growth chamber. Greenhouse irradiance reduction treatments resulted in alterations in whole-plant source-sink relationships. Total plant dry weight and overall plant quality were reduced in shaded plants. The depletion rate of mother bulb dry matter was not affected by reduced irradiance, whereas daughter bulb reserve loss was increased by irradiance reduction treatments. There was no daughter bulb reserve remobilization in plants grown in complete darkness after FBI. Flower bud and open flower dry weights were progressively reduced as irradiance was reduced. With an 85% irradiance reduction, plants forced from 17.5-cm bulbs had 63% bud abortion, whereas, with 20.0-cm bulbs, only 12% of the buds aborted. Plants grown in complete darkness after FBI became etiolated, and flowers failed to open. These results demonstrate differences in the ability of various morphological regions of the bulb to respond to reductions in greenhouse irradiance. Since the daughter bulb response to reduced irradiance was relatively slow, additional remobilization of dry matter from the daughter bulb is probably of minimal benefit during short periods of reduced irradiance in commercial greenhouses.
P.I. Garriz, G.M. Colavita, and H.L. Alvarez
Crop load and the genetic biological carrying capacity (source–sink relationships) determine the potential for fruit size development on apple; however, the environment within which the fruit grows attenuates this potential. The effects of different crop loads on the growth pattern and the progress of maturity in apples were evaluated at the Comahue National Univ., Argentina (lat. 38 56'S long 67 59'W), during the 1998–99 growing season. Our experiment was conducted on 6-year-old `Braeburn'/Malling Merton 111 apple (Malus domestica Borkh.) trees spaced 4.0 × 2.3 m and trained to palmette leader. Treatments were 1) light crop load (LC), 2.5 fruit/cm2 trunk cross-sectional area (TCSA), 2) moderate crop load (MC), 6.5 fruit/cm2 TCSA (standard commercial crop load) and 3) high crop load (HC), minimum 8 fruit/cm2 TCSA, no fruit removed from tree. Whole trees were hand-thinned 19 days after full bloom (DAFB). Fruit diameter (FD) was taken at two weekly intervals (n = 24 per date and treatment) and maturity indexes were determined at harvest. Analysis of variance was used and mean separations were computed with Student's t test. From 38 DAFB until harvest, fruit size was significantly reduced (P < 0.01) in the HC trees, indicating that they were source-limited during growth. At 166 DAFB, FD was 7.48, 7.14, and 6.89 cm for the LC, MC and HC treatments, respectively. Adequate carbon was apparently available to support a commercial crop load since no differences were found between LC and MC trees. Crop level influenced flesh firmness; at 173 DAFB, it was significantly lower in HC trees than MC and LC trees (84.33, 92.51, and 91.57 N, respectively). These results suggest some goals of thinning for ensuring sizable `Braeburn' fruit.
Jingwei Dai and Robert E. Paull
The growth and development of Anthurium andraeanum Andre cv. Kaumana flower before and after emergence from the subtending leaf base was studied. Eighty days before emergence, the anthurium flower was =0.3 cm long, enclosed by two tightly rolled stipules at the base of the subtending leaf petiole. During the rapid elongation stage of the leaf petiole, the flower (0.8 to 1.0 cm long) entered a period of slow growth 40 to 60 days before flower emergence. After the subtending leaf blade unfurled and had a positive photosynthetic rate, flower growth resumed. Spathe color development started =28 days before emergence when the flower was =50% of the emergence flower length (4.5 cm). At flower emergence, the spathe, excluding the lobes, was =75% red. The lobes did not develop full redness until 7 to 10 days after emergence. Peduncle growth was sigmoidal with the maximum growth rate 21 days after emergence. Spathe growth is characterized by a double sigmoid curve. The young, growing, subtending leaf blade had a negative net photosynthetic rate. Removal of this leaf blade advanced flower emergence by 18 days. The soft green leaf (25 to 30 days after leaf emergence) had a slightly positive measured net photosynthetic rate, and the removal of this leaf resulted in flower emergence 11 days earlier. A mature subtending leaf had the highest measured net photosynthetic rate, and its removal had little effect on flower emergence. The subtending leaf acted as a source of nutrients required for the developing flower. Altering the source-sink relationship by leaf removal accelerated flower emergence, probably by reducing the slow growth phase of the flower.
Desmond R. Layne and J.A. Flore
The source-sink ratio of l-year-old, potted `Montmorency' sour cherry (Prunus cerasus) trees was manipulated by partial defoliation (D) or continuous lighting (CL) to investigate the phenomenon of end-product inhibition of photosynthesis. Within 24 hours of D, net CO2 assimilation rate (A) of the most recently expanded source leaves of D plants was significantly higher than nondefoliated (control) plants throughout the diurnal photoperiod. Between 2 and 7 days after D, A was 30% to 50% higher and stomatal conductance rate (g,) was 50% to 100% higher than in controls. Estimated carboxylation efficiency(k) and ribulose-1,5-bisphosphate (RuBP) regeneration rate increased significantly within 2 days and remained consistently higher for up to 9 days after D. Leaf starch concentration and dark respiration rate decreased but sorbitol and sucrose concentration increased after D. The diurnal decline in A in the afternoon after D may have been due to feedback inhibition from accumulation of soluble carbohydrates (sucrose and sorbitol) in the cytosol. This diurnal decline indicated that trees were sink limited. By 9 days after D, photochemical efficiency was significantly higher than in control plants. In the long term, leaf senescence was delayed as indicated by higher A and gs in combination with higher chlorophyll content up to 32 days after D. CL resulted in a significant reduction of A, gs, k, variable chlorophyll fluorescence (Fv), photochemical efficiency, and estimated RuBP regeneration rate of the most recently expanded source leaves within 1 day. During the exposure to CL, A was reduced 2- to 3-fold and k was reduced up to 4-fold. The normal linear relationship between A and gs was uncoupled under CL indicating that A was not primarily limited by gs and since internal CO2 concentration was not significantly affected, the physical limitation to A imposed by the stomata was negligible. The decrease in Fv and photochemical efficiency indicated that leaves were photoinhibited within 1 day. The decrease in instantaneous chlorophyll fluorescence after at least 1 day of CL indicated that there was a reversible regulatory mechanism whereby the damage to photosystem II reaction centers was repaired. Leaf chlorophyll content was not altered by 1,2, or 3 days of exposure to CL, indicating that photooxidation of chlorophytl did not occur. The time to full photosynthetic recovery from CL increased as the duration of exposure increased. CL plants that were photoinhibited accumulated significant starch in the chloroplast in a companion study (Layne and Flore, 1993) and it is possible that an orthophosphate limitation in the chloroplast stroma was occurring. D plants that were continuously illuminated were not photosynthetically inhibited. After 7 days of CL, plants that were then partially defoliated yet remained in CL photosynthetically recovered within 5 days to pre-CL values. Under the conditions of this investigation, end-product inhibition of A occurred in young, potted sour cherry trees but the mechanism of action in D plants was different than in CL plants.
Sorkel Kadir, Gaganpreet Sidhu, and Kassim Al-Khatib
Thermotolerance of photosynthesis and productivity in `Chandler' and `Sweet Charlie' strawberry plants (Fragaria ×ananassa Duch.) exposed to three temperature regimes was studied. Net CO2 assimilation rate (A), variable chlorophyll fluorescence (Fv), efficiency of photosystem II (Fv/Fm), relative chlorophyll content, plant growth, and fruit yield and quality were measured. High temperature (40 °C day/35 °C night) was more detrimental to photosynthesis and productivity than the moderate or low temperature (30/25 or 20/15 °C). Net CO2 assimilation rate in both cultivars was markedly reduced by 40/35 °C, although there was slight decline in `Sweet Charlie' at 30/25 °C. `Chandler' maintained significantly higher A rates than `Sweet Charlie' for at least three weeks of heat stress, indicating that `Chandler' might tolerate longer exposure to high temperature. In parallel to the decrease in A rate, intercellular CO2 concentration (Ci) and instantaneous water use efficiency (WUE) were significantly decreased at high temperature. `Chandler' leaves were cooler and transpired more than `Sweet Charlie' leaves, suggesting that each cultivar adopted different heat resistance mechanisms at 40/35 °C. There were changes in Fv and Fv/Fm with increasing temperature, indicating irreversible damage to photosystem II at 40/35 °C might have occurred. The trend of reduction in stomatal conductance (g S) in both cultivars at high temperature did not coincide with the reduction in A rates. Decline in A rates at high temperature was more related to changes in Fv/Fm than to g S activity. The optimal temperature for vegetative growth was 30/25 °C. Reduction in A rate at high temperature resulted in reduction in total leaf area (LA), shoot, root, and leaf biomasses. Strawberry roots were more responsive than shoot growth to temperatures above 20/15 °C. Fruit yield for `Chandler' was higher at 20/15 °C than at 30/25 °C, suggesting that `Chandler' might have a higher source-to-sink relationship at 20/15 °C than at 30/25 °C. Fruit skin color was temperature dependent only for `Chandler'. A quadratic relationship between flower development and duration of exposure to 30/25 °C for both cultivars was observed; more than two weeks of 30/25 °C can be detrimental to flower development. Regardless of the cultivar and duration of exposure, 40/35 °C was the temperature regime most detrimental to fruit set.
Marlene Ayala and Gregory Lang
( Tables 4 and 5 ). Conversely, Kappel (1991) reported that, with ‘Lambert’ sweet cherry on vigorous P. avium seedling rootstocks, ES growth had a greater sink strength for photosynthates than fruit. Source–sink relationships and relative C
Rebecca L. Darnell, Nicacio Cruz-Huerta, and Jeffrey G. Williamson
effects on overall growth, cell number, and cell size in bell pepper ovaries Ann. Bot. (Lond.) 110 987 994 10.1093/aob/mcs173 Hall, A.J. Milthorpe, F.L. 1978 Assimilate source-sink relationships in Capsicum annuum L. 3. Effects of fruit excision on
Jieshan Cheng, Peige Fan, Zhenchang Liang, Yanqiu Wang, Ning Niu, Weidong Li, and Shaohua Li
Crop yield and fruit quality in fruit trees are highly dependent on efficient capture of solar energy and subsequent allocation of photoassimilate. Source-sink relationships are important factors influencing these allocation patterns. Fruit