Consumption of fruit and vegetable crops rich in lutein and β-carotene carotenoids is associated with reduced risk of cancers and aging eye diseases. Kale (Brassica oleracea L. var. acephala D.C.) ranks highest for lutein concentrations and is an excellent source of dietary carotenoids. Kale plants were grown under varied photoperiods to determine changes in the accumulation of fresh and dry biomass, chlorophyll a and b, and lutein and β-carotene carotenoids. The plants were cultured in a controlled environment using nutrient solutions under photoperiod treatments of 6, 12, 16, or 24 hours (continuous). Fresh and dry mass production increased linearly as photoperiod increased, reaching a maximum under the 24-hour photoperiod. Maximum accumulation of lutein, β-carotene, and chlorophyll b occurred under the 24-h photoperiod at 13.5, 10.4, and 58.6 mg/100 g fresh mass, respectively. However, maximum chlorophyll a (235.1 mg/100 g fresh mass) occurred under the 12-hour photoperiod. When β-carotene and lutein were measured on a dry mass basis, the maximum accumulation was shifted to the 16-hour photoperiod. An increase in photoperiod resulted in increased pigment accumulation, but maximum concentrations of pigments were not correlated with maximum biomass production.
Mark G. Lefsrud, Dean A. Kopsell, Robert M. Augé, and A.J. Both
A.J. Both, E. Reiss, J.F. Sudal, K.E. Holmstrom, C.A. Wyenandt, W.L. Kline, and S.A. Garrison
The impact of a manually operated energy curtain on the recorded nighttime inside air and soil temperatures, relative humidity (RH), and daily light integrals during early-season high tunnel tomato (Lycopersicon esculentum) production in central and southern New Jersey were examined. Environmental data (air and soil temperatures, RH, and photosynthetically active radiation) were collected from late March through mid-May at two New Jersey locations for the 2004 and 2005 growing seasons. The continued impact of the early use of an energy curtain was further evaluated by collecting light, temperature, and marketable fruit yield data for the remainder of both growing seasons for one of the two experimental sites. Results showed that although the use of the curtain modestly increased early season nighttime inside air and soil temperatures and RH, the curtain reduced accumulated light integral during the first 7 weeks after transplanting and resulted in a marginal early yield increase. The main benefit of the energy curtain occurred on cold nights when an early season crop might otherwise be exposed to potentially damaging low temperatures.
Mark Lefsrud, Dean Kopsell, Carl Sams, Jim Wills, and A.J. Both
Drying of spinach (Spinacia oleracea L.) and kale (Brassica oleracea L. var. acephala D.C.) is required to determine percentage of dry matter (%DM) and pigment concentration of fresh leaves. ‘Melody’ spinach and ‘Winterbor’ kale were greenhouse-grown in hydroponic nutrient solutions containing 13 or 105 mg·L−1 N. Using vacuum freeze dryers and convection ovens, plant tissues were dried for 120 h at five different temperature treatments: 1) freeze drying at −25 °C; 2) freeze drying at 0 °C; 3) vacuum drying at +25 °C; 4) oven drying at +50 °C; and 5) oven drying at +75 °C. Spinach leaf tissue %DM was affected, but kale %DM was unaffected by drying temperature. Spinach and kale leaf tissue %DM were both affected by N level. The high N spinach decreased from 7.3 to 6.4%DM when drying temperature increased from +25 to +75 °C. The low N spinach decreased from 12.7 to 9.6%DM as the drying temperature increased from −25 to +50 °C. Kale averaged from 14.8%DM for the high N treatment and from 21.8%DM for the low N treatment. However, drying temperature did not have a significant impact on measured %DM in kale. Lutein, β-carotene, and chlorophyll levels for both spinach and kale leaf tissue were affected by drying temperature. Measured concentrations of all pigments decreased over 70% as the drying temperature increased from −25 to 75 °C. The largest pigment fresh and dry weight concentrations for spinach and kale were measured at drying temperatures below +25 °C. The spinach and kale samples dried between −25 and +25 °C were not significantly different from each other in %DM or pigment concentration measured on a dry or fresh weight basis. Thus, drying leaf tissue for accurate pigment analysis requires temperatures below +25 °C using vacuum or freeze drying technology.
David S. de Villiers, Robert W. Langhans, A.J. Both, Louis D. Albright, and Sue Sue Scholl
CO2 enrichment increases efficiency of light utilization and rate of growth, thereby reducing the need for supplemental lighting and potentially lowering cost of production. However, during warmer periods of the year, CO2 enrichment is only possible intermittently due to the need to vent for temperature control. Previous research investigated the separate and combined effects of daily light integral and continuous CO2 enrichment on biomass accumulation in lettuce. The current research was designed to look at the efficiency with which lettuce is able to utilize intermittent CO2 enrichment, test the accuracy with which growth can be predicted and controlled, and examine effects of varying CO2 enrichment and supplemental lighting on carbon assimilation and plant transpiration on a minute by minute basis. Experiments included application of various schedules of intermittent CO2 enrichment and gas exchange analysis to elucidate underlying physiological processes. Same-day and day-to-day adjustments in daily light integrals were made in response to occasional CO2 venting episodes, using an up-to-the-minute estimate of growth progress based on an integration of growth increments that were calculated from actual light levels and CO2 concentrations experienced by the plants. Results indicated lettuce integrates periods of intermittent CO2 enrichment well, achieving expected growth targets as measured by destructive sampling. The gas-exchange work quantified a pervasive impact of instantaneous light level and CO2 concentration on conductance and CO2 assimilation. Implications for when to apply supplemental lighting and CO2 enrichment to best advantage and methods for predicting and controlling growth under intermittent CO2 enrichment are discussed.
Robin G. Brumfield, Laura B. Kenny, Alyssa J. DeVincentis, Andrew K. Koeser, Sven Verlinden, A.J. Both, Guihong Bi, Sarah T. Lovell, and J. Ryan Stewart
Greenhouse growers find themselves under increasing pressure to respond to consumer preferences to use environmentally sustainable practices and materials while maintaining profitable operations. These consumer preferences reflect a mounting awareness of the environmental issues, such as climate change and their associated social costs. Ideally, sustainable horticultural production accounts for both traditional economic considerations and such social costs, some of which can be explained through the calculation of global warming potential (GWP). An obvious candidate for a sustainable intervention is the traditional plastic pot, which growers can replace with alternative biocontainers with varying degrees of GWP. This study calculates the variability of direct costs of production using alternative containers to offer a comparison of social and economic costs. We evaluated these direct costs of producing petunia (Petunia ×hybrida) grown in pots made of traditional plastic, bioplastic, coir, manure, peat, bioplastic sleeve, slotted rice hull, solid rice hull, straw, wood fiber, and recycled reground plastic containers used in a previous assessment of GWP. Our analysis of the costs when using a traditional plastic pot showed that the highest contributors to GWP were different from the highest contributors to direct costs, revealing that the price does not reflect the environmental impact of several inputs. Electricity, the plastic shuttle tray, and the plastic pot contributed most to GWP, whereas labor, the plastic container, and paclobutrozol growth regulator contributed most to direct cost of production (COP). At 64% of total cost, labor was the most expensive input. Watering by hand added another $0.37–$0.54 per plant in labor. When we analyzed input costs of each alternative container separately, container type had the largest impact on total direct costs. Before adding container costs, the direct COP ranged from $0.56 to $0.61 per plant. After adding containers, costs ranged from $0.61 to $0.97 per plant. Wood fiber pots were the most expensive and recycled reground plastic pots were the least expensive in this study. Based on our assessment and the observed small variation in GWP between alternative containers, growers would benefit from selecting a container based on price and consumer demand. Some social costs that we are not aware of yet may be associated with some or all biocontainers.