A comparative study of young ‘Thompson Seedless’ grapevines (Vitis vinifera L.) under drip and furrow irrigation. II. Growth, water use efficiency and nitrogen partitioning

The response of 3-year-old grapevines (Vitis vinifera L. cultivar ‘Thompson Seedless’) to furrow and drip irrigation was quantified in terms of water status, growth, and water use efficiency (WUE). Drip irrigation was applied daily according to best estimates of vineyard evapotranspiration while furrow irrigations were applied when 50% of the plant available soilwater content had been depleted. Drip and furrow irrigated vines showed similar water status (midday leaf water potential, Ψ₁) and shoot growth patterns throughout the season. Dry weight partitioning was not significantly different between treatments but root mass was somewhat larger for the furrow than drip irrigated vines. Nitrogen concentrations of the fruit and roots were significantly (P < 0.05) less for the drip irrigated vines when compared with the furrow treatment. Similar WUE (kg water kg⁻¹ fresh fruit wt.) were obtained for both treatments indicating that furrow irrigation was as efficient as drip irrigation under the conditions of this study. The data indicate that drip irrigation may increase the potential for control of vine growth by making vines more dependent on irrigation and N fertilization than furrow irrigation.     

Dynamics of anthocyanin and flavonol profiles in the ‘Crimson Seedless’ grape berry skin during development and ripening

‘Crimson Seedless’ grapes (Vitis vinifera L.) do not develop adequate berry colour in different parts of the world including Australia and USA leading to serious economic losses to the growers. In the present study, various anthocyanins and flavonols were identified in the skin of the ‘Crimson Seedless’ grape berries using LC/PDA/ESI-MS and their changes in the berry skin during development and ripening of ‘Crimson Seedless’ grape berries were investigated during 2005–2006 and 2006–2007. Eleven anthocyanins and two flavonols were identified in the berry skin using LC/PDA/ESI-MS. Of the anthocyanins identified, four anthocyanins including cyanidin 3-O-(6″-O-acetyl)-glucoside, peonidin 3-O-(6″-O-acetyl)-glucoside, malvidin 3-O-(6″-O-acetyl)-glucoside and malvidin 3-O-(6″-O-coumaroyl)-glucoside were not reported earlier. During both the years, the concentration of the 3-O-glucosides of delphinidin, petunidin, peonidin, and malvidin as well as the acetyl and coumaroyl esters of the 3-O-glucosides of cyanidin, peonidin, and malvidin in the berry skin increased during berry development and ripening. During 2006–2007, the concentration of cyanidin 3-O-glucoside in the berry skin increased during the early stages of berry ripening and subsequently declined till harvest while in 2005–2006, the concentration increased during the initial phase of berry ripening and remained relatively stable thereafter till harvest. The concentration of total anthocyanins in the berry skin was higher during 2006–2007 as compared to 2005–2006. During both years, the concentration of quercetin 3-O-glucoside in the berry skin increased during berry development and ripening while the concentration of quercetin 3-O-glucuronide in the berry skin decreased during the same period. To the best of our knowledge, this is the first report on the evolution of different anthocyanins and flavonols in the ‘Crimson Seedless’ berry skin during berry development and ripening.     

Capability of the ‘Ball-Berry’ model for predicting stomatal conductance and water use efficiency of potato leaves under different irrigation regimes

The capability of the ‘Ball-Berry’ model (BB-model) in predicting stomatal conductance (g_s) and water use efficiency (WUE) of potato (Solanum tuberosum L.) leaves under different irrigation regimes was tested using data from two independent pot experiments in 2004 and 2007. Data obtained from 2004 was used for model parameterization, where measurements of midday leaf gas exchange of potted potatoes were done during progressive soil drying for 2 weeks at tuber initiation and earlier bulking stages. The measured photosynthetic rate (A_n) was used as an input for the model. To account for the effects of soil water deficits on g_s, a simple equation modifying the slope (m) based on the mean soil water potential (Ψ_s) in the soil columns was incorporated into the original BB-model. Compared with the original BB-model, the modified BB-model showed better predictability for both g_s and WUE of potato leaves on the parameterization data set. The models were then tested using the data from 2007 where plants were subjected to four irrigation regimes: non-irrigation (NI), full irrigation (FI), partial root-zone drying (PRD), and deficit irrigation (DI) for 3 weeks during tuber initiation and earlier bulking stages. The simulation results showed that the modified BB-model better simulated g_s for the NI and DI treatments than the original BB-model, whilst the two models performed equally well for predicting g_s of the FI and PRD treatments. Although both models had poor predictability for WUE (0.47 < r² < 0.71) of potato leaves, the modified BB-model was able to distinguish the effects of the irrigation regimes on WUE being that the WUE was generally greater for PRD than for FI and DI plants. Conclusively, the modified BB-model is capable of predicting g_s and of accounting for the differential effects of irrigation regimes on WUE of potato leaves. This information is valuable for further simulating potato water use thereby optimizing WUE under field conditions.     

Effects of N–P–K deficiency and temperature regime on the growth and development of Lilium longiflorum ‘Nellie White’ during bulb production under phytotron conditions

One-year-old scale bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under a combination of six constant day/night temperature regimes and five N–P–K nutrient treatments under short days for 107 d (growing period 1 or GP-1) to compare the effects on growth and development and bulb production. Results during GP-1 were as follows: failure of bulblets to produce a shoot (“no-shows”) was found at high temperatures (30/26 and 26/22 °C) and not influenced by the nutrient treatments. Flower bud abortion was observed in the minus-N, minus-P, and minus-N–P–K treatments at high temperatures (30/26 or 26/22 °C), but not observed at any temperatures in the complete and minus-K treatments. The loss of bulb fresh weight in minus-N treated bulblets was less than in the other treatments resulting in less root and shoot growth in the minus-N treatment. At the intermediate temperatures where growth was highest, omission of N, P, K, or all three resulted in losses in stem bulb fresh weight, stem plus leaf fresh weight, number of flowers, and stem root fresh weight. Omission of N, P, or all three nutrients resulted in lowest basal root fresh weight. Bulb N and K concentrations were lowest in plants grown with complete nutrient solution at the two coldest temperature regimes (14/10 and 10/6 °C). Bulb P concentration was lowest at the three coldest (18/14, 14/10 and 10/6 °C) and the warmest (30/26 °C) temperature regimes. Stem length was shorter when P was omitted. Omission of any of the three nutrients resulted in lower concentrations of the other nutrients. The one exception was where low K did not affect N concentration. In the second phase of the experiment, plants grown at 18/14 °C and irrigated with the complete nutrient solution for 107 d (GP-1) were continued at this day/night temperature regime and five N–P–K nutrient treatments for another 89 d under long days (growing period 2 or GP-2). Results during GP-2 were as follows. Basal bulb yield was not impacted by omission of N, P, or K, or all three. Of all growth measurements, only stem plus leaf fresh weight was lower and only when all three nutrients (minus-N–P–K) were omitted. At the end of GP-2, basal bulb concentrations of N and P did not differ from the concentrations in bulbs at the beginning of GP-1; however, K concentration was lower at the end of GP-2. Omission of N or P further resulted in lower bulb K concentration, suggesting that a moderate supply of N, P, and K be applied during GP-2 since an additional year of bulb production is needed to produce forcing-sized bulbs.     

Growth and development of Lilium longiflorum ‘Nellie White’ during bulb production under controlled environments : I. Effects of constant,variable and greenhouse day/night temperature regimes on scale and stem bulblets

One-year-old scale and stem bulblets of Lilium longiflorum Thunb. ‘Nellie White’ (Easter lily) were grown under constant and variable growth chamber conditions and greenhouse conditions to compare growth and development and bulb production. Eight temperatures regimes were established using the following: six growth chambers set to provide day/night temperature regimes of 30/26, 26/22, 22/18, 18/14, 14/10 and 10/6 °C; a seventh growth chamber (VAR) programmed to begin at 22/18 °C, then decline in three 4–5 week steps to 10/6 °C, and subsequently increase in three 4–5 week steps to 22/18 °C to simulate seasonal field temperatures in the coastal bulb production area of northern California and southern Oregon; and a double layer polyethylene greenhouse (GH) set to begin cooling at 22 °C and heating at 18 °C. Ten percent of the scale bulblets and 35% of the stem bulblets failed to develop shoots (“no-shows”). “No-shows” increased with increasing temperature with a significant number starting at 18/14 °C. The moderately high GH temperature also induced “no-shows”. Maximum basal bulb (the main planted bulb) weight occurred at 26/22 °C for both bulblet types. Scale bulblets not only produced heavier basal bulbs with a larger circumference than stem bulblets, but also produced heavier stem bulbs. Stem bulb formation and production was maximized in the range of 18/14–26/22 °C and in the GH for scale bulblets. Stem bulb production from stem bulblets did not differ from zero. Scale bulblets produced more basal and stem roots than the stem bulblets at the end of the early growth period, but there was no significant difference at the end of the study. Root fresh weight was greatest in the range of 14/10–18/14 °C and declined at higher or lower temperatures. The VAR and GH treatments had similar root weights to those at 18/14 °C. Shoot length was maximized at 22/18 °C for stem bulblets and in the GH and at 22/18 °C for scale bulblets. Stem plus leaf (shoot) fresh weight was not statistically different between bulblet types with the exception of an increased weight for stem bulblets grown at 22/18 °C. Scale bulblets in the GH had greater stem plus leaf weights than scale bulblets in the other temperature regimes. Shoot leaf number was highest in stem bulblets at 22/18 °C and in the GH. In these two temperature treatments, more leaves were produced by stem bulblets than scale bulblets. In all other treatments, there was no significant difference in leaf number. Bulblet type had no effect on number of flowers produced. Flower number was maximum in the range 10/6–22/18 °C, decreased at 26/22 °C and in the GH, and was absent at 30/26 °C. For bulb production, reduced flowering is desired since flowers are generally removed during the outdoor bulb production period. Meristem abortion, which also causes a desirable reduction in flowers, was greater in scale bulblets. It occurred at 26/22 °C and was greater at 30/26 °C. Scale bulbs produced the largest main bulbs, with a maximum yield at 26/22 °C.