Techniques for trace element analysis: x-ray fluorescence, x-ray excitation with protons, and flame atomic absorption.
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Blood Chemical Analysis↗
Biomedical subjects
R M Wheeler
Publications and source records attributed to R M Wheeler.
Soybean stem growth under high-pressure sodium with supplemental blue lighting.
High-pressure sodium (HPS) lamps are popular for plant lighting because of their high energy conversion efficiencies. Yet their spectrum has very little blue light (BL), which may cause undesirable morphological responses. To study this, McCall' soybean [Glycine max (L.) Merr.] plants were grown for 28 d in growth chambers using HPS lamps, with or without supplemental light from blue phosphor fluorescent lamps. Total photosynthetic photon flux (PPF) levels (including blue fluorescent) were kept near 300 or 500 micromoles m-2 s-1. Blue fluorescent levels ranged from 7 to 20 micromoles m-2 s-1, providing from 6 to 18 micromoles m-2 s-1 of supplemental BL (400-500 nm). Stem and internode lengths were longest under 300 micromoles m-2 s-1 HPS lighting and became progressively shorter with increasing supplemental BL until a total of approximately 30 micromoles m-2 s-1 of BL (from HPS and BL supplement) was present in the spectrum. Beyond this, extra BL had no effect. Two other lamps rich in BL, metal halide (Optimarc) and fluorescent (Vita-Lite), also produced plants with short stems, as did HPS lighting maintained at 500 micromoles m-2 s-1. Results suggest that use of high-pressure sodium or other blue-deficient sources for lighting at low to moderate photosynthetic photon flux levels may cause abnormal stem elongation, but this can be prevented by adding a small amount of supplemental blue light.
Light↗
Carbon dioxide effects on potato growth under different photoperiods and irradiance.
Carbon dioxide concentration can exert a strong influence on plant growth, but this influence can vary depending on irradiance. To study this, potato plants (Solanum tuberosum L.) cultivars Norland', Russet Burbank', and Denali' were grown in controlled-environment rooms at different levels of CO2 and irradiance. Carbon dioxide levels were maintained either at 350 or 1000 micromoles mol-1 and applied in combination with 12- or 24-h photoperiods at 400 or 800 micromoles m-2 s-1 photosynthetic photon flux. Air temperatures and relative humidity were held constant at 16 degrees C and 70%, respectively, and plants were harvested 90 d after planting. When averaged across all cultivars, CO2 enrichment increased tuber yield and total plant dry weight by 39 and 34%, respectively, under a 12-h photoperiod at 400 micromoles m-2 s-1; 27 and 19% under 12 h at 800 micromoles m-2 s-1; 9 and 9% under 24h at 400 micromoles m-2 s-1. It decreased dry weights by 9 and 9% under 24 h at 800 micromoles m-2 s-1. Tuber yield of Denali showed the greatest increase (21%) in response to increased CO2 across all irradiance treatments, while tuber yields of Russet Burbank and Norland were increased 18 and 9%, respectively. The results show a pattern of greater plant growth from CO2 enrichment under lower PPF and a short photoperiod.
Carbon Dioxide↗
Gas exchange characteristics of wheat stands grown in a closed, controlled environment.
Information on gas exchange of crop stands grown in controlled environments is limited, but is vital for assessing the use of crops for human life-support in closed habitats envisioned for space. Two studies were conducted to measure gas exchange of wheat stands (Triticum aestivum L. cv. Yecora Rojo) grown from planting to maturity in a large (20 m2 canopy area), closed growth chamber. Daily rates of dark-period respiration and net photosynthesis of the stand were calculated from rates of CO2 build-up during dark cycles and subsequent CO2 drawdown in the light (i.e., a closed-system approach). Lighting was provided as a 20-h photoperiod by high-pressure sodium lamps, with canopy-level photosynthetic photon flux density (PPFD) ranging from 500 to 800 micromoles m-2 s-1 as canopy height increased. Net photosynthesis rates peaked near 27 micromoles CO2 m-2 s-1 at 25 d after planting, which corresponded closely with stand closure, and then declined slowly with age. Similarly, dark-period respiration rates peaked near 14 micromoles CO2 m-2 s-1 at 25 d and then gradually declined with age. Responses to short-term changes in irradiance after canopy closure indicated the stand light compensation point for photosynthesis to be near 200 micromoles m-2 s-1 PPFD. Tests in which CO2 concentration was raised to approximately 2000 micromoles mol-1 and then allowed to draw down to a compensation point showed that net photosynthesis was nearly saturated at > 1000 micromoles mol-1; below approximately 500 micromoles mol-1, net photosynthesis rates dropped sharply with decreasing CO2. The CO2 compensation point for photosynthesis occurred near 50 micromoles mol-1. Short-term (24 h) temperature tests showed net photosynthesis at 20 degrees C > or = 16 degrees C > 24 degrees C, while dark-period respiration at 24 degrees C > 20 degrees C > 16 degrees C. Rates of stand evapotranspiration peaked near Day 25 and remained relatively constant until about Day 75, after which rates declined slowly. Results from these tests will be used to model the use of plants for CO2 removal, O2 production, and water evaporation for controlled ecological life support systems proposed for extraterrestrial environments.
Carbon Dioxide↗
Gas exchange in NASA's biomass production chamber: a preprototype closed human life support system.
An important aspect of environmental control in a life-support system is the monitoring and regulation of atmospheric gases (Sager et al. 1988) at concentrations required for the maintenance of all life forms. It will be necessary to know the rates of CO2 use, oxygen evolution, and water flux through evapotranspiration by a crop stand under various environmental conditions, so that appropriate designs and control systems for maintaining mass balances of those gases can be achieved for a full range of environmental regimes. Mass budgets of gases will also enable evaluation of crop health by monitoring directly the rates of gas exchange and indirectly the rate of accumulation of dry matter, based on rates of carbon dioxide use. This article focuses on the unique capabilities of the NASA biomass production chamber for monitoring and evaluating gas exchange rates, with special emphasis on results with wheat and soybean, two candidate species identified by NASA for CELSS.
Biomass↗