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  • Author or Editor: K. Hill x
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The effects of within-channel spacings (WCS; 13, 18, 25 cm) and between-channel spacings (BCS; 13, 25,38 cm) on yield and linear growth rate of sweetpotatoes [Ipomoea batalas (L.) Lam.] grown by use of the nutrient film technique (NFT) were evaluated. Storage root count, fresh and dry weights, and linear growth rate, expressed as root area, declined linearly in response to decreased BCS, while fresh and dry foliage weight decreased linearly and quadratically as spacing was reduced within the growth channels. Neither linear growth rate on a canopy area basis nor the edible biomass index was significantly affected by WCS or BCS.

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`Georgia Red' peanut (Arachis hypogaea L.) was grown hydroponically at 20/16 °C, 24/20 °C, 28/24 °C, and 32/28 °C, day/night air temperatures to evaluate effects on pod and seed yield, flowering, harvest index, and oil content. Ten-day-old peanut seedlings were transplanted into rectangular nutrient film technique troughs (0.15 × 0.15 × 1.2 m) and grown for 110 days. Growth chamber conditions were as follows: photosynthetic photon flux (PPF) mean of 436 μmol·m-2·s-1, 12 h light/12 h dark cycle, and 70% ± 5% relative humidity. The nutrient solution used was a modified half-Hoagland with pH and electrical conductivity maintained between 6.5 to 6.7, and 1000 to 1300 μS·cm-1, respectively, and was replenished weekly. Vegetative growth (foliage, stem growth, total leaf area, and leaf number) was substantially greater at increasingly warmer temperatures. Reproductive growth was significantly influenced by temperature. Flowering was extremely sensitive to temperature as the process was delayed or severely restricted at 20/16 °C. The number of gynophores decreased with temperature and was virtually nonexistent at the lowest temperature. Pod yield increased with temperatures up to 28/24 °C but declined by 15% at the highest temperature (32/28 °C). Seed yield, maturity, and harvest index were highest at 28/24 °C. Oil content (percent crude fat) increased an average of 23% and was highest at the warmest temperature (32/28 °C). These results clearly suggest that vegetative and reproductive growth, as well as oil content of peanut in controlled environments, are best at warmer temperatures of 28/24 °C to 32/28 °C than at cooler temperatures of 20/16 °C to 24/20 °C.

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A greenhouse study was conducted to evaluate the influence of harvest intervals on biomass yield and omega fatty acids of ‘Golden purslane’ (Portulaca oleracea). Nutrients were supplied as a modified full-strength Hoagland solution two to three times weekly. Plants were harvested sequentially at 20, 40, and 60 days after transplanting (DAT) corresponding to 42, 63, and 84 days after sowing. Fatty acids were determined using a gas chromatography–mass spectrometry. Harvest intervals significantly influenced foliage fresh and dry weight, leaf number and plant height, and root length and fresh weight and were greatest at 60 DAT. Fatty acid analysis verified the presence of myristate, palmitate, linoleate, and linolenate at 20 DAT and in all three harvests, whereas stearate and oleate were detected only in the last two harvests (40 and 60 DAT). Linoleate, palminate, and linolenate were the most abundant fatty acids in purslane with levels in excess of 300 mg·kg−1. Those for myristate, stearate, and oleate were in excess of 200 mg·kg−1. The ratio of omega-6/omega-3 ranged from 0.44 for Harvest 1 to 1.1 for Harvest 3, whereas ratios for harvest intervals two and three were equal to or greater than the recommended daily human requirement. Results showed qualitative and quantitative differences of harvest intervals of purslane, suggesting that an optimal ratio of omega-6 to omega-3 fatty acids can be achieved ≈20 DAT.

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Growth chamber experiments were conducted to study the physiological and growth response of sweetpotato [Ipomoea batatas (L.) Lam.] to either 50% or 85 % relative humidity (RH). Vine cuttings of T1-155 were grown using the nutrient film technique in a randomized complete-block design with two replications. Temperature regimes of 28/22C were maintained during the light/dark periods with irradiance at canopy level of 600 μmol·m-2·s-1 and a 14/10-hour photoperiod. High RH (85%) increased the number of storage roots per plant and significantly increased storage root fresh and dry weight, but produced lower foliage fresh and dry weight than plants grown at 50% RH. Edible biomass index and linear growth rate (in grams per square meter per day) were significantly higher for plants grown at 85 % than at 50% RH. Leaf photosynthesis and stomatal conductance were higher for plants at 85 % than at 50% RH. Thus, the principal effect of high RH on sweetpotato growth was the production of higher storage root yield, edible biomass, growth rate, and increased photosynthetic and stomatal activity.

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Two sweetpotato [Ipomoea batatas (L.) Lam] genotypes (`Georgia Jet' and the breeding clone TI-155) were grown at 12-, 15-, 18-, and 21-h light/12-, 9-, 6-, 3-h dark cycles, respectively, to evaluate their growth and elemental concentration responses to duration and amount of daily lighting. Vine cuttings (15 cm long) of both genotypes were grown in rectangular nutrient film technique channels for 120 days. Conditions were as follows: photosynthetic photon flux (PPF) mean 427 μmol·m–2·s–1, 28C day/22C night air cycle, and 70% ± 5% relative humidity. The nutrient solution used was a modified half-strength Hoagland's solution. Storage root count per plant and per unit area, yield (in grams per square meters per day), and harvest index increased, while production efficiency (in grams per mole) decreased with increased daily PPF. Stomatal conductance for both genotypes declined with increased daily PPF. Leaves were smallest for both genotypes at the 21-h light period, while storage root yield declined as leaf area index increased. Except for a linear decrease in leaf N and K with increased light period, elemental concentration was not significantly influenced.

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Growth chamber experiments were conducted to study the physiological and growth response of peanut (Arachis hypogaea L.) to 50% and 85% relative humidity (RH). The objective was to determine the effects of RH on pod and seed yield, harvest index, and flowering of peanut grown by the nutrient film technique (NFT). `Georgia Red' peanut plants (14 days old) were planted into growth channels (0.15 × 0.15 × 1.2 m). Plants were spaced 25 cm apart with 15 cm between channels. A modified half-Hoagland solution with an additional 2 mm Ca was used. Solution pH was maintained between 6.4 and 6.7, and electrical conductivity (EC) ranged between 1100 and 1200 μS·cm–1. Temperature regimes of 28/22 °C were maintained during the light/dark periods (12 hours each) with photosynthetic photon flux (PPF) at canopy level of 500 μmol·m–2·s–1. Foliage and pod fresh and dry weights, total seed yield, harvest index (HI), and seed maturity were greater at high than at low RH. Plants grown at 85% RH had greater total and individual leaflet area and stomatal conductance, flowered 3 days earlier and had a greater number of flowers reaching anthesis. Gynophores grew more rapidly at 85% than at 50% RH.

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Growth chamber experiments were conducted to evaluate the effect of irradiance and daily light period on storage root yield and leaf elemental concentration of two sweetpotato cultivars grown hydroponically by use of the nutrient film technique (NFT). Stem cuttings (15 cm) of cv. Whatley/Loretan and Georgia Jet were grown in NFT channels (0.15 × 0.15 × 1.2 m) in reach-in growth chambers under light period/irradiance combinations of 18 h: 300 μmol·m−2·s−1 or 9 h: 600 μmol·m−2·s−1 photosynthetic photon flux. Temperature was 28/22 °C light/dark with a relative humidity of 70% ± 5%. Storage root and foliage yields were greater in both cultivars exposed to a longer daily light period and lower irradiance. The main effect of cultivar indicated that storage root yield was significantly greater among plants of ‘Whatley/Loretan’ compared with that of ‘Georgia Jet’, whereas foliage yield was similar between cultivars. Leaves of plants grown under longer daily light period and lower irradiance had significantly lower concentrations of all elements, nitrogen, phosphorus, potassium, calcium, magnesium, manganese, iron, calcium, boron, and zinc, except for calcium, manganese, and boron. There were no significant differences in leaf elemental concentration between cultivars. Thus, a longer daily light and lower irradiance enhanced biomass production of sweetpotato but reduced leaf elemental concentration probably because of a “dilution” effect.

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Two sweetpotato [Ipomoea batatas (L.) Lam] genotypes (TU-82-155 and NCC-58) were grown hydroponically and subjected to a temporary loss of lighting in the form of 14 days of prolonged darkness compared with a lighted control under standard daily light periods to determine the impact on growth responses and storage root yield. Vine cuttings of both genotypes were grown in rectangular channels. At 65 days after planting, lights were turned off in the treatment chambers and replaced by a single incandescent lamp, providing between 7 and 10 µmol·m−2·s−1 photosynthetic photon flux (PPF) for 18 hours, and the temperature lowered from 28/22 °C light/dark, to a constant 20 °C. Plants remained under these conditions for 14 days after which the original light level was restored. Growth chamber conditions predark included, a PPF mean provided by 400-W metal halide lamps, of 600 ± 25 µmol·m−2·s−1, an 18-hour light/6-hour dark cycle and a relative humidity of 70% ± 5%. The nutrient solution used was a modified half-Hoagland with pH and electrical conductivity (EC) maintained between 5.5–6.0 and 1000–1200 μS·cm−1, respectively, and was adjusted weekly. Storage root number and fresh weight were similar regardless of treatments. Plants exposed to prolonged darkness produced 10.5% and 25% lower fibrous root fresh and dry mass, respectively, but similar foliage yield and harvest index (HI). ‘NCC-58’ produced an average of 31% greater storage root yield than that of ‘TU-82-155’ but the number of storage roots as well as % dry matter (%DM) were similar. ‘NCC-58’ also produced 31% greater fibrous root dry weight, whereas ‘TU-82-155’ produced a 44% greater HI. The significant interaction between prolonged darkness and cultivars for %DM of the storage roots showed that DM for ‘TU-82-155’ was 18.4% under prolonged darkness and 17.9% in the light. That for ‘NCC-58’ was 16.4% under prolonged darkness compared with 19.4% (14.8% greater) for plants that were not subjected to prolonged darkness. The evidence that there were no adverse impacts on storage root yield following the exposure to prolonged darkness suggests that the detrimental effects were below the detectable limits for these cultivars in response to the short perturbation in the available light and that sweetpotatoes would be hardy under short-term failure situations.

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The effects of elevated CO2 on growth, pod, and seed yield, and gas exchange of `Georgia Red' peanut (Arachis hypogaea L.) were evaluated under controlled environmental conditions. Plants were exposed to concentrations of 400 (ambient), 800, and 1200 μmol·mol–1 CO2 in reach-in growth chambers. Foliage fresh and dry weights increased with increased CO2 up to 800 μmol·mol–1, but declined at 1200 μmol·mol–1. The number and the fresh and dry weights of pods also increased with increasing CO2 concentration. However, the yield of immature pods was not significantly influenced by increased CO2. Total seed yield increased 33% from ambient to 800 μmol·mol–1 CO2, and 4% from 800 to 1200 μmol·mol–1 CO2. Harvest index increased with increasing CO2. Branch length increased while specific leaf area decreased linearly as CO2 increased from ambient to 1200 μmol·mol–1. Net photosynthetic rate was highest among plants grown at 800 μmol·mol–1. Stomatal conductance decreased with increased CO2. Carboxylation efficiency was similar among plants grown at 400 and 800 μmol·mol–1 and decreased at 1200 μmol·mol–1CO2. These results suggest that CO2 enrichment from 400 to 800 μmol·mol–1 had positive effects on peanut growth and yield, but above 800 μmol·mol–1 enrichment seed yield increased only marginally.

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