limit the transferability of the results resulting from regional, climatic, and site-specific variables. In fact, no controlled environment research could be found evaluating low-temperature N uptake, metabolism, and use of turfgrass or the response
Daniel T. Lloyd, Douglas J. Soldat and John C. Stier
Chieri Kubota, Cynthia A. Thomson, Min Wu and Jamal Javanmardi
extended to Controlled Environment Agriculture Program and EuroFresh Farms for the technical and financial support.
Manette Schönfeld and Cary A. Mitchell
121 ORAL SESSION (Abstr. 613-620) CROSS-COMMODITY GROWTH CHAMBERS AND CONTROLLED ENVIRONMENTS
Thomas S.C. Li, K.E. Bedford and P.L. Sholberg
Traditionally, American ginseng (Panax quinquefolium L.) seeds are stratified for 18 to 22 months, before seeding, in a sandbox buried outdoors in late August or early September. Uncontrolled fluctuating temperature and moisture levels and the presence of pathogenic organisms in the seed box can cause seeds to sprout prematurely, rot, dry out and die. A study was initiated to shorten the lengthy stratification period, and to increase seed viability and percentage of germination by stratifying seeds indoors under a controlled environment. Seeds were subjected to various periods of warm [15 or 20 °C (59 or 68 °F)] and cold [2 °C (35.6 °F)] temperature stratification regimes in growth chambers. Embryo growth and viability, and seed moisture content were tested periodically during stratification. The best warm regime for embryo development, seed viability and germination after subsequent cold treatment was 15 °C (59 °F). The first “split” seeds, indicating incipient germination, were observed after 3 months of warm [15 °C (59 °F)] and 4 months of cold [2 °C (35.6 °F)] treatment, when average embryo length reached 6 mm (0.24 inch). Greenhouse germination of stratified seeds was as high as 80%. The results from this study indicate that good germination is possible when ginseng seeds are stratified indoors under a controlled environment and seeds can be made to germinate at any time of the year.
David R. Dreesen and Robert W. Langhans
Abbreviations: CEGR, controlled environment growth rooms; HI, high irradiante levels; LI, low irradiance levels; MHI, medium high irradiance levels; MLI, medium low irradiance levels 1 Former graduate research assistant, currently research associate
Norman R. Scott, Corinne Johnson Rutzke and Louis D. Albright
One of the deterrents to the commercial adoption of controlled-environment agriculture (CEA) on a broad scale is the significant energy cost for lighting and thermal environmental control. Advances in energy conversion technologies, such as internal combustion engines (ICs), microturbines and fuel cells, offer the potential for combined heat and power (CHP) systems, which can be matched with the needs of CEA to reduce fossil-based fuels consumption. A principal concept delineated is that an integrated entrepreneurial approach to create business and community partnerships can enhance the value of energy produced (both electrical and heat). Energy production data from a commercial dairy farm is contrasted with energy use data from two greenhouse operations with varying energy-input requirements. Biogass produced from a 500-cow dairy combined with a 250-kW fuel cell could meet nearly all of the energy needs of both the dairy and an energy-intensive 740-m2 CEA greenhouse lettuce facility. The data suggest CEA greenhouses and other closely compatible enterprises can be developed to significantly alter agriculture, as we have known it.
Harry Janes, James Cavazzoni, Guna Alagappan, David Specca and Joseph Willis
A qualitative systems approach to controlled environment agriculture (CEA) is presented by means of several multi-institutional projects integrated into a demonstration greenhouse at the Burlington County Resource Recovery Complex (BCRRC), N.J. The greenhouse has about 0.4 ha of production space, and is located about 800 m from the about 40-ha BCRRC landfill site. A portion of the landfill gas produced from the BCRRC site is used for microturbine electricity generation and for heating the greenhouse. The waste heat from the turbines, which are roughly 15 m from the greenhouse, is used as the main heat source for the greenhouse in the winter months, and to desalinate water when heating is not required. Recovery of this waste heat increases the energy efficiency of the four 30-kW turbines from about 25% to 75%. Within the greenhouse, aquaculture and hydroponic crop production are coupled by recycling the aquaculture effluent as a nutrient source for the plants. Both the sludge resulting from the filtered effluent and the inedible biomass from harvested plants are vermicomposted (i.e., rather than being sent to the landfill), resulting in marketable products such as soil amendments and liquid plant fertilizer. If suitably cleaned of contaminants, the CO2 from the landfill gas may be used to enrich the plant growing area within the greenhouse to increase the yield of the edible products. Landfill gas from the BCRRC site has successfully been processed to recover liquid commercial grade CO2 and contaminant-free methane-CO2, with the potential for this gas mixture to be applied as a feedstock for fuel cells or for methanol production. Carbon dioxide from the turbine exhaust may also be recovered for greenhouse enrichment. Alternatively, algal culture may be used to assimilate CO2 from the turbine exhaust into biomass, which may then be used as a biofuel, or possibly as fish feed, thus making the system more self-contained. By recycling energy and materials, the system described would displace fossil fuel use, mitigating negative environmental impacts such as greenhouse gas emissions, and generate less waste in need of disposal. Successful implementation of the coupled landfill (gas-to-energy · aquaponic · desalination) system would particularly benefit developing regions, such as those of the Greater Caribbean Basin.
Charles F. Forney and David G. Brandl
Solutions of glycerol and water provide a convenient and inexpensive system to control the relative humidity (RH) in small controlled-environment chambers. The relationship between the specific gravity (SG) of a glycerol-water solution and its equilibrium RH is described by the equation SG = [-0.189 (RH) + 19.9]0.0806. Gas can be humidified by bubbling it through jars containing solutions of glycerol-water with the desired equilibrium RH. The effects of flow rate, volume of solution, temperature, and pressure on the equilibrium RH are discussed.
K.S. Yourstone and D.H. Wallace
This study was undertaken to determine whether plastochron index (PI), a mathematical construct that quantifies shoot development, can be applied to indeterminate bean (Phaseolus vulgaris L.) genotypes. Length measurements of the middle trifoliate leaflet were the basis of the PI calculation. The expansion of each middle trifoliate leaflet at every node on each plant tested was measured over time to determine whether the growth pattern of each leaflet fits the assumptions of the PI construct. Plants from five indeterminate bean genotypes were grown in two controlled environments: A constant 29C with 12-hr of daylength, and a constant 23C with 12-hr daylength extended to 14 hr with low light intensity. Early leaflet expansion was exponential for all five genotypes in both environments. Expansion rates of successive leaflets were also similar, although a few leaflets in three of the 10 genotype-environment combinations differed in their rates of expansion. Exponential and equal rates of expansion validate the calculation of the fractional component of the PI. In both environments, all genotypes exhibited an increasing rate of leaf initiation with time, which precludes the use of a simple linear slope in estimating rate of development.
Jorge M. Fonseca, James W. Rushing, Nihal C. Rajapakse, Ronald L. Thomas and Melissa B. Riley
The purpose of this review is to promote a discussion about the potential implications of herb production in controlled environments, focusing on our recent works conducted with feverfew. Research suggests that the content of secondary metabolites in medicinal plants fluctuates with changing environmental conditions. Our studies with feverfew (Tanacetum parthenium [L.] Schultz-Bip., Asteraceae) lend support to this hypothesis. Feverfew plants exposed to different water and light conditions immediately before harvest exhibited changes in content of some secondary metabolites. The highest yield of parthenolide (PRT) was in plants that received reduced-water regimes. Phenolics concentration however, was higher in plants receiving daily watering. Light immediately before harvest enhanced accumulation of PRT, but reduced the phenolic content. Notably, PRT decreased at night whereas total phenolics decreased during the photoperiod and increased at night. PRT also increased with increased plant spacing. UV light supplementation increased PRT only in plants that had undergone water stress, whereas phenolics increased when UV was applied to continuosly watered plants. Clearly, production of medicinal plants under greenhouse conditions is a promising method for controlling levels of phytochemicals through manipulation of light and water as discussed here, and possibly other environmental factors such as temperature and daylength. However, better understanding of how the environment alter secondary metabolite levels is needed as it was revealed that manipulating the environment to favor increased accumulation of one group of phytochemicals could result in a decline of other key metabolites.