Raymond M. Wheeler
Raymond M. Wheeler
Raymond M. Wheeler, Barbara V. Peterson and Gary W. Stutte
Ethylene production by 10 or 20 m2 stands of wheat, soybean, lettuce, potato, and tomato was monitored throughout growth and development in an atmospherically closed plant chamber. Chamber ethylene levels varied among species and rose during periods of canopy expansion and rapid growth for all species. Following this, ethylene levels either declined during seed fill and maturation for wheat and soybean, or remained relatively constant for potato and tomato (during flowering and early fruit development). Lettuce plants were harvested during rapid growth and peak ethylene production. Chamber ethylene levels increased rapidly during tomato ripening, reaching concentrations about 10 times that measured during vegetative growth. The highest ethylene production rates during vegetative growth ranged from 1.6 to 2.5 nmol·m-2·d-1 during rapid growth of lettuce and wheat stands, or about 0.3 to 0.5 nmol·g-1 fresh weight per hour. Estimates of stand ethylene production during tomato ripening showed that rates reached 43 nmol·m-2·d-1 in one study and 93 nmol·m-2·d-1 in a second study with higher lighting, or about 50× that of the rate during vegetative growth of tomato. In a related test with potato, the photoperiod was extended from 12 to 24 hours (continuous light) at 58 days after planting (to increase tuber yield), but this change in the environment caused a sharp increase in ethylene production from the basal rate of 0.4 to 6.2 nmol·m-2·d-1. Following this, the photoperiod was changed back to 12 h at 61 days and ethylene levels decreased. The results suggest three separate categories of ethylene production were observed with whole stands of plants: 1) production during rapid vegetative growth, 2) production during climacteric fruit ripening, and 3) production from environmental stress.
Kenneth A. Corey, Phil A. Fowler and Raymond M. Wheeler
Reduced atmospheric pressures may be used to minimize mass and engineering requirements for plant growth habitats used in some extraterrestrial applications. A chamber with high vacuum capability and thermal control at Kennedy Space Center was used to measure water loss of lettuce plants at reduced atmospheric pressures. A test stand with three, high-pressure sodium vapor lamps was used to determine short-term plant responses to reduced pressure. Initial experiments with lettuce showed that a pressure of 10 kPa (≈0.1 atm) resulted in a 6.1-fold increase in the rate of water loss compared to water loss at ambient pressure. However, due to low relative humidity, plants wilted after 30 minutes exposure to 10 kPa. A follow-up experiment in which relative humidity was controlled between 70% and 85%, demonstrated that water loss was directly proportional to the vapor pressure gradient, regardless of atmospheric pressure in the pressure range of 10 to 101 kPa. However, the response was curvilinear, suggesting effects on the pathway resistance. Results indicate that plant growth at atmospheric pressures of 5 to 10 kPa should be achievable. Further work will necessitate better relative humidity control and carbon dioxide control in order to separate vapor pressure deficit effects from diffusion effects.
Gary W. Stutte, Neil C. Yorio and Raymond M. Wheeler
The effect of photoperiod (PP) on net carbon assimilation rate (Anet) and starch accumulation in newly mature canopy leaves of `Norland' potato (Solanum tuberosum L.) was determined under high (412 ∝mol·m-2·s-1) and low (263 ∝mol·m-2·s-1) photosynthetic photon flux (PPF) conditions. The Anet decreased from 13.9 to 11.6 and 9.3 μmol·m-2·s-1, and leaf starch increased from 70 to 129 and 118 mg·g-1 drymass (DM) as photoperiod (PP) was increased from 12/12 to 18/6, and 24/0, respectively. Longer PP had a greater effect with high PPF conditions than with low PPF treatments, with high PPF showing greater decline in Anet. Photoperiod did not affect either the CO2 compensation point (50 μmol·mol-1) or CO2 saturation point (1100-1200 μmol·mol-1) for Anet. These results show an apparent limit to the amount of starch that can be stored (≈15% DM) in potato leaves. An apparent feedback mechanism exists for regulating Anet under high PPF, high CO2, and long PP, but there was no correlation between Anet and starch concentration in individual leaves. This suggests that maximum Anet cannot be sustained with elevated CO2 conditions under long PP (≥12 hours) and high PPF conditions. If a physiological limit exists for the fixation and transport of carbon, then increasing photoperiod and light intensity under high CO2 conditions is not the most appropriate means to maximize the yield of potatoes.
Gregory D. Goins, Neil C. Yorio and Raymond M. Wheeler
The National Aeronautics and Space Administration (NASA) has been conducting controlled environment research with potatoes (Solanum tuberosum L.) in recirculating nutrient film technique (NFT)-hydroponic systems as a human life support component during long-duration spaceflight. Standard nutrient solution management approaches include constant pH regulation with nitric acid (HNO3) and daily adjustment of electrical conductivity (EC) equivalent to half-strength modified Hoagland's solution, where nitrate (NO3-) is the sole nitrogen (N) source. Although tuber yields have been excellent with such an approach, N use efficiency indices are expected to be low relative to tuber biomass production. Furthermore, the high amount of N used in NFT-hydroponics, typically results in high inedible biomass, which conflicts with the need to minimize system mass, volume, and expenditure of resources for long-duration missions. More effective strategies of N fertilization need to be developed to more closely match N supply with demand of the crop. Hence, the primary objective of this study was to identify the optimal N management regime and plant N requirement to achieve high yields and to avoid inefficient use of N and excess inedible biomass production. In separate 84-day cropping experiments, three N management protocols were tested. Treatments which decreased NO3 --N supply indirectly through lowering nutrient solution EC (Expt. I), or disabling pH control, and/or supplying NH4 +-N (Expt. III) did not significantly benefit tuber yield, but did influence N use efficiency indices. When supplied with an external 7.5 mm NO-3 --N for the first 42 days after planting (DAP), lowered to 1.0 mm NO3 -N during the final 42 days (Expt. II), plants were able to achieve yields on par with plants which received constant 7.5 mm NO3 --N (control). By abruptly decreasing N supply at tuber initiation in Expt. II, less N was taken up and accumulated by plants compared to those which received high constant N (control). However, proportionately more plant accumulated N was used (N use efficiency) to produce tuber biomass when N supply was abruptly lowered at tuber initiation in Expt. II. Hence, a hydroponic nutrient solution N management system may be modified to elicit greater plant N-use while maintaining overall high tuber yield as opposed to achieving high tuber yields through excess N supply and shoot growth.
Hyeon-Hye Kim, Gregory D. Goins, Raymond M. Wheeler and John C. Sager
Plants will be an important component of future long-term space missions. Lighting systems for growing plants will need to be lightweight, reliable, and durable, and light-emitting diodes (LEDs) have these characteristics. Previous studies demonstrated that the combination of red and blue light was an effective light source for several crops. Yet the appearance of plants under red and blue lighting is purplish gray making visual assessment of any problems difficult. The addition of green light would make the plant leave appear green and normal similar to a natural setting under white light and may also offer a psychological benefit to the crew. Green supplemental lighting could also offer benefits, since green light can better penetrate the plant canopy and potentially increase plant growth by increasing photosynthesis from the leaves in the lower canopy. In this study, four light sources were tested: 1) red and blue LEDs (RB), 2) red and blue LEDs with green fluorescent lamps (RGB), 3) green fluorescent lamps (GF), and 4) cool-white fluorescent lamps (CWF), that provided 0%, 24%, 86%, and 51% of the total PPF in the green region of the spectrum, respectively. The addition of 24% green light (500 to 600 nm) to red and blue LEDs (RGB treatment) enhanced plant growth. The RGB treatment plants produced more biomass than the plants grown under the cool-white fluorescent lamps (CWF treatment), a commonly tested light source used as a broad-spectrum control.
Neil C. Yorio, Gregory D. Goins, Hollie R. Kagie, Raymond M. Wheeler and John C. Sager
Radish (Raphanus sativus L. cv. Cherriette), lettuce (Lactuca sativa L. cv. Waldmann's Green), and spinach (Spinacea oleracea L. cv. Nordic IV) plants were grown under 660-nm red light-emitting diodes (LEDs) and were compared at equal photosynthetic photon flux (PPF) with either plants grown under cool-white fluorescent lamps (CWF) or red LEDs supplemented with 10% (30 μmol·m-2·s-1) blue light (400-500 nm) from blue fluorescent (BF) lamps. At 21 days after planting (DAP), leaf photosynthetic rates and stomatal conductance were greater for plants grown under CWF light than for those grown under red LEDs, with or without supplemental blue light. At harvest (21 DAP), total dry-weight accumulation was significantly lower for all species tested when grown under red LEDs alone than when grown under CWF light or red LEDs + 10% BF light. Moreover, total dry weight for radish and spinach was significantly lower under red LEDs + 10% BF than under CWF light, suggesting that addition of blue light to the red LEDs was still insufficient for achieving maximal growth for these crops.
Guntur V. Subbarao, Raymond M. Wheeler, L.H. Levine and Gary W. Stutte
Accumulation of glycinebetaine occurs in Chenopodiaceae members and is thought to assist in osmotic adjustment and protect cytoplasm from sodium toxicity. Red beet has an ability to tolerate high tissue sodium levels, which may result in increased glycinebetaine production. To test this hypothesis, two cultivars of red beet ['Scarlet Supreme' (SS) and `Ruby Queen' (RQ)] were grown under nonsaline (4.75 mM Na) and saline (54.75 mM Na) conditions in a recirculating hydroponic system for 42 days at elevated CO2 (1200 μmol•mol-1) in a growth chamber. Leaf glycinebetaine level, relative water content, and osmotic potential were measured at weekly intervals. Leaf glycinebetaine levels increased with plant age and reached a maximum of 67 μmol•g-1 dw under nonsaline and 101 μmol•g-1 dry weight (dw) under saline conditions at 42 days in SS; in RQ, the glycinebetaine levels reached a maximum of 91 μmol•g-1 dw under nonsaline and 121 μmol•g-1 dw under saline conditions by 26 days. The mean glycinebetaine levels were increased over two-thirds under saline conditions in both the cultivars. RQ accumulated significantly higher (37% more under nonsaline, and 46% more under salinity) glycinebetaine than SS. The turgid leaf osmotic potential of RQ was consistently higher than SS under nonsaline (2.23 MPa in RQ vs. 1.82 MPa in SS) and saline (2.48 MPa in RQ vs. 2.02 MPa in SS) conditions. The results indicate that higher glycinebetaine levels in the leaf could result in better osmotic adjustment, and glycinebetaine accumulation in red beet can vary among cultivars and is strongly affected by external salinity.
Gioia D. Massa, Hyeon-Hye Kim, Raymond M. Wheeler and Cary A. Mitchell
Light-emitting diodes (LEDs) have tremendous potential as supplemental or sole-source lighting systems for crop production both on and off earth. Their small size, durability, long operating lifetime, wavelength specificity, relatively cool emitting surfaces, and linear photon output with electrical input current make these solid-state light sources ideal for use in plant lighting designs. Because the output waveband of LEDs (single color, nonphosphor-coated) is much narrower than that of traditional sources of electric lighting used for plant growth, one challenge in designing an optimum plant lighting system is to determine wavelengths essential for specific crops. Work at NASA's Kennedy Space Center has focused on the proportion of blue light required for normal plant growth as well as the optimum wavelength of red and the red/far-red ratio. The addition of green wavelengths for improved plant growth as well as for visual monitoring of plant status has been addressed. Like with other light sources, spectral quality of LEDs can have dramatic effects on crop anatomy and morphology as well as nutrient uptake and pathogen development. Work at Purdue University has focused on geometry of light delivery to improve energy use efficiency of a crop lighting system. Additionally, foliar intumescence developing in the absence of ultraviolet light or other less understood stimuli could become a serious limitation for some crops lighted solely by narrow-band LEDs. Ways to prevent this condition are being investigated. Potential LED benefits to the controlled environment agriculture industry are numerous and more work needs to be done to position horticulture at the forefront of this promising technology.