This study was designed to characterize the mechanisms of N-stimulated peach Prunus persica (L.) Batsch productivity. The effects of N fertilization on potential assimilate availability (source capacity) and on the growth capacity of individual fruit (sink capacity) were assessed. On heavily thinned trees, fertilization did not stimulate fruit growth rates relative to those on nonfertilized trees, suggesting that fruit growth rates were not assimilate-limited throughout the period of fruit development. However, N fertilization resulted in a longer fruit development period and increased the growth potential of individual fruit by 20% (fresh mass) and 15% (dry mass) vs. controls. In unthinned trees, N fertilization increased total fruit yield by 49% (fresh mass) and 40% (dry mass) compared to the unthinned, nonfertilized controls. N fertilization increased total fruit yield per tree in unthinned peach trees by extending the fruit development period and thus increasing the amount of assimilate accumulated for fruit growth. The fruit development period was prolonged both by assimilate deprivation associated with increasingly higher crop loads and by N fertilization. Thus, the prolongation of the peach fruit development period by N-fertilization appears inconsistent with the role of N in increasing assimilate availability for fruit growth. We conclude that N fertilization stimulates peach yields by increasing the period for fruits to use assimilates (sink capacity). The effect of N on assimilate availability was not directly evaluated. The timing of fertilizer N availability did not influence fruit growth potential.
J.L. Saenz, T.M. DeJong, and S.A. Weinbaum
evaluated the relative growth rates to compare plant growth rate at different growth stages. To determine the plant growth rate from transplanting to harvesting, we calculated the relative growth rate between 10 and 35 d after sowing (RGR DAS35 ). However
Marc van Iersel
Container size can affect the growth and development of bedding plants. The effects of widely differing container sizes on growth and development of salvia (Salvia splendens F. Sellow ex Roem. & Schult.) were quantified. Plants were grown in a greenhouse in 7.3-, 55-, 166-, and 510-mL containers. Container volume affected plant growth as early as 18 days after planting. Growth was positively correlated with pot size and differences increased throughout most of the growing period. Growth of the plants in the 7.3-mL cells was reduced because of a low net assimilation rate (4.34 g·m-2·d-1), compared to the plants in the 55-, 166-, and 510-mL pots (≈5.44 g·m-2·d-1). Plants in 510-mL containers grew faster than those in 55- and 166-mL containers because of a higher leaf area ratio. Both lateral branching and leaf expansion were suppressed by root restriction and flowering was delayed. The growth rate of plants in 166-mL pots declined after the onset of flowering, and final plant size was comparable for plants in 55- and 166-mL pots. Although water deficit stress or nutrient deficiencies cannot be excluded as contributing factors, these were probably not the main reason for observed differences.
Marjorie Reyes-Díaz, Claudio Inostroza-Blancheteau, Rayen Millaleo, Edgardo Cruces, Cristián Wulff-Zottele, Miren Alberdi, and María de la Luz Mora
different Al treatments in the same conditions mentioned above. At the end of the experiment (20 d), the Al-treated plants were harvested for fresh and dry weight determinations (W 2 ). Growth was expressed as the relative growth rate (RGR) from the mean
Edgar L. Vinson III, Kaitlyn J. Price, J. Raymond Kessler, Elina D. Coneva, Masuzyo Mwanza, and Matthew D. Price
weights were combined to determine plant weight. Relative growth rate (RGR) was calculated using the following equation ( Fernandez et al., 2001 ): R G R = l n P D W 2 − l n P D W 1 T 2 − T 1 , where lnPDW2 is the natural log of plant dry weight 2
than continuous light, and large seeds than small seeds in the early seedling stage. Table 3. Shoot height (SH), average growth height (AGH), and relative growth rate (RGR) of large and small seeds in C. bungei at 15 (T15), 20 (T20), and 25 °C (T25
Jer-Chia Chang and Tzong-Shyan Lin
) characterized fruit growth of ‘73-S-20’, an irregular bearing line of ‘No Mai Tsz’ litchi found in JiJi, Nantou, central Taiwan (lat. 23°N) ( Yen et al., 1984 ) and documented that during the peak periods of the fruit, relative growth rate (RGR in dry weight
Anke van der Ploeg, Ranathunga J.K.N. Kularathne, Susana M.P. Carvalho, and Ep Heuvelink
in SD. With the dry weight and leaf area observations collected in Expt. 2, relative growth rate (RGR), net assimilation rate (NAR), leaf area ratio (LAR), specific leaf area (SLA), and leaf weight ratio (LWR) were calculated over the LD period
Jun Zhu, Duane P. Bartholomew, and Guillermo Goldstein
Despite the potential impact of rising global CO2 levels, only a limited number of studies have been conducted on the effects of ambient and elevated CO2 on plants having Crassulacean acid metabolism (CAM). To our knowledge, there are no studies for pineapple [Ananas comosus (L.) Merr.], the most commercially important CAM plant. Pineapple plants were grown at CO2 levels of ≈330 (ambient) and ≈730 (elevated) μmol·mol-1 in open-top chambers for 4 months. The mean air temperature in the chambers was ≈39 °C day/24 °C night. Average plant dry mass at harvest was 180 g per plant at elevated CO2 and 146 g per plant at ambient CO2. More biomass was partitioned to stem and root but less to leaf for plants grown at elevated CO2; leaf thickness was 11% greater at elevated than at ambient CO2. The diurnal difference in leaf titratable acidity (H+) at elevated CO2 reached 347 mmol·m-2, which was up to 42% greater than levels in plants grown in ambient CO2. Carbon isotopic discrimination (Δ) of plants was 3.75% at ambient CO2 and 3.17% at elevated CO2, indicating that CO2 uptake via the CAM pathway was enhanced more by elevated CO2 than uptake via the C3 pathway. The nonphotochemical quenching coefficient (qN) of leaves was ≈45% lower in the early morning for plants grown at elevated than at ambient CO2, while afternoon values were comparable. The qN data suggested that the fixation of external CO2 was enhanced by elevated CO2 in the morning but not in the afternoon when leaf temperature was ≥40 °C. We found no effect of CO2 levels on leaf N or chlorophyll content. Pineapple dry matter gain was enhanced by elevated CO2, mainly due to increased CO2 dark fixation in environments with day temperatures high enough to suppress C3 photosynthesis.
Ming Li and Wei-tang Song
treatment. These results coincide with those of Yelle (1990) . Hence, the change in plant responses to eCO 2 can be detected with these methods. Fig. 10. Relative growth rate ( RGR ) of Angelica transplants calculated based on the estimated dry weight of