ABSTRACT
The behavior of water in weightlessness, as occurs in orbiting spacecraft, presents multiple challenges for plant growth. Soils remain saturated, impeding aeration, and leaf surfaces remain wet, impeding gas exchange. Herein we report developmental and biochemical anomalies of "Super Dwarf" wheat (Triticum aestivum L.) grown aboard Space Station Mir during the 1996-97 "Greenhouse 2" experiment. Leaves of Mir-grown wheat were hyperhydric, senesced precociously and accumulated aromatic and branched-chain amino acids typical of tissues experiencing oxidative stress. The highest levels of stress-specific amino acids occurred in precociously-senescing leaves. Our results suggest that the leaf ventilation system of the Svet Greenhouse failed to remove sufficient boundary layer water, thus leading to poor gas exchange and onset of oxidative stress. As oxidative stress in plants has been observed in recent space-flight experiments, we recommend that percentage water content in apoplast free-spaces of leaves be used to evaluate leaf ventilation effectiveness. Mir-grown plants also tillered excessively. Crowns and culms of these plants contained low levels of abscisic acid but high levels of cytokinins. High ethylene levels may have suppressed abscisic acid synthesis, thus permitting cytokinins to accumulate and tillering to occur.
Subject(s)
Air Movements , Oxidative Stress/physiology , Plant Leaves/physiology , Space Flight , Triticum/growth & development , Water/physiology , Weightlessness/adverse effects , Environment, Controlled , SpacecraftABSTRACT
We carried out three experiments with Super Dwarf wheat in the Bulgarian/Russian growth chamber Svet (0.1 m2 growing area) on the Space Station Mir. This paper mostly describes the first of these NASA-supported trials, began on Aug. 13, 1995. Plants were sampled five times and harvested on Nov. 9 after 90 days. Equipment failures led to low irradiance (3, then 4 of 6 lamp sets failed), instances of high temperatures (ca. 37 degrees C), and sometimes excessive substrate moisture. Although plants grew for the 90 d, no wheat heads were produced. Considering the low light levels, plants were surprisingly green, but of course biomass production was low. Plants were highly disoriented (low light, mirror walls?). Fixed and dried samples and the root module were returned on the U.S. Shuttle Atlantis on Nov. 20, 1995. Samples of the substrate, a nutrient-charged zeolite called Balkanine, were taken from the root module, carefully examined for roots, weighed, dried, and reweighed. The Svet control unit and the light bank were shipped to Moscow. An experiment validation test (EVT) of plant growth and experimental procedures, carried out in Moscow, was highly successful. Equipment built in Utah to measure CO2, H2O vapor, irradiance, air and leaf (IR) temperature, O2, pressure, and substrate moisture worked well in the EVT and in space. After this manuscript was first prepared, plants were grown in Mir with a new light bank and controller for 123 d in late 1996 and 39 days in 1996/1997. Plants grew exceptionally well with higher biomass production than in any previous space experiment, but the ca. 280 wheat heads that were produced in 1996 contained no seeds. Ethylene in the cabin atmosphere was responsible.
Subject(s)
Environment, Controlled , Seeds/growth & development , Space Flight/instrumentation , Triticum/growth & development , Weightlessness , Culture Media , Environmental Monitoring/instrumentation , Equipment Design , Equipment Failure , Ethylenes/pharmacology , Light , Plant Growth Regulators/pharmacology , Seeds/drug effects , Seeds/radiation effects , Triticum/drug effects , Triticum/radiation effects , ZeolitesABSTRACT
The SVET Greenhouse on-board the Orbital Station Mir was used to measure canopy photosynthesis and transpiration rates for the first time in space. During the Greenhouse IIB experiment on Mir (June-January 1997), carbon and water vapor fluxes from two wheat (cv. Superdwarf) canopies were measured using the US developed Gas Exchange Measurement System (GEMS). Gas analyzers capable of resolving CO2 concentration differences of 5 micromoles mol-1 against a background of 0.9% CO2, are necessary to measure photosynthetic and respiratory rates on Mir. The ability of the GEMS gas analyzers to measure these CO2 concentration differences was determined during extensive ground calibrations. Similarly, the sensitivity of the analyzers to water vapor was sufficient to accurately measure canopy evapotranspiration. Evapotranspiration, which accounted for over 90% of the water added to the root zone, was estimated using gas exchange and used to estimate substrate moisture content. This paper presents canopy photosynthesis and transpiration data during the peak vegetative phase of development in microgravity.
Subject(s)
Environmental Monitoring , Photosynthesis/physiology , Plant Transpiration/physiology , Space Flight/instrumentation , Triticum/metabolism , Weightlessness , Air Conditioning/instrumentation , Carbon Dioxide/metabolism , Environment, Controlled , Plant Roots/metabolism , Triticum/growth & development , Water/metabolismABSTRACT
Wheat (Triticum aestivum L.) plants were grown under four irradiance levels: 1,400, 400, 200, and 100 micromol m-2 s-1. Leaves and roots were sampled before, during, and after the boot stage, and levels of abscisic acid (ABA), indole-3-acetic acid (IAA), zeatin, zeatin riboside, dihydrozeatin, dihydrozeatin riboside, isopentenyl adenine, and isopentenyl adenosine were quantified using noncompetitive indirect ELISA systems. Levels of IAA in leaves and roots of plants exposed to 100 micromol m-2 s-1 of irradiance were 0.7 and 2.9 micromol kg-1 dry mass (DM), respectively. These levels were 0.2 and 1.0 micromol kg-1 DM, respectively, when plants were exposed to 1,400 micromol m-2 s-1. Levels of ABA in leaves and roots of plants exposed to 100 micromol m-2 s-1 were 0.65 and 0.55 micromol kg-1 DM, respectively. They were 0.24 micromol kg-1 DM (both leaves and roots) when plants were exposed to 1,400 micromol m-2 s-1. Levels of isopentenyl adenosine in leaves (24.3 nmol kg-1 DM) and roots (29.9 nmol kg-1 DM) were not affected by differences in the irradiance regime. Similar values were obtained in a second experiment. Other cytokinins could not be detected (<10 nmol kg 1 DM) in either experiment with the sample sizes used (150-600 mg DM for roots and shoots, respectively).
Subject(s)
Abscisic Acid/metabolism , Cytokinins/metabolism , Indoleacetic Acids/metabolism , Light , Triticum/metabolism , Triticum/radiation effects , Abscisic Acid/radiation effects , Indoleacetic Acids/radiation effects , Photons , Photoperiod , Plant Growth Regulators/metabolism , Plant Growth Regulators/radiation effects , Plant Leaves/metabolism , Plant Leaves/radiation effects , Plant Roots/metabolism , Plant Roots/radiation effectsABSTRACT
Super-Dwarf wheat plants were grown in growth chambers under 12 treatments with three photoperiods (18 h, 21 h, 24 h) and four carbon dioxide (CO2) levels (360, 1,200, 3,000 and 7,000 micromoles mol-1). Carbon dioxide concentrations affected flower initiation rates of Super-Dwarf wheat. The optimum CO2 level for flower initiation and development was 1,200 micromoles mol-1. Super-optimum CO2 levels delayed flower initiation, but did not decrease final flower bud number per head. Longer photoperiods not only accelerated flower initiation rates, but also decreased deleterious effects of super-optimum CO2. Flower bud size and head length at the same developmental stage were larger under longer photoperiods, but final flower bud number was not affected by photoperiod.
Subject(s)
Carbon Dioxide/pharmacology , Photoperiod , Triticum/growth & development , Dose-Response Relationship, Drug , Environment, Controlled , Space Flight , Time Factors , Triticum/drug effects , Triticum/radiation effects , WeightlessnessABSTRACT
Three monoclonal antibodies (all IgG1) were prepared against the plant cytokinin dihydrozeatin riboside (diH[9R]Z) and characterized for suitability in the isolation and quantification of dihydrozeatin-type phytohormones. These antibodies detected as little as 5-10 pg of the homologous cytokinin when used in both competitive and noncompetitive immunoassays and each had characteristic crossreactivity with structurally-related cytokinins. One antibody was used to quantify HPLC-purified diH[9R]Z recovered from wheat tissue. The same antibody also was linked to an insoluble support for use in affinity purification of a mixture of cytokinins. These antibodies will be useful for purification and quantification of dihydrozeatin and its 9-riboside and 9-glucoside in plant tissue.
Subject(s)
Antibodies, Monoclonal , Cytokinins/immunology , Animals , Cross Reactions , Enzyme-Linked Immunosorbent Assay , Female , Hybridomas/metabolism , Mice , Mice, Inbred BALB C , Oxidoreductases/metabolism , Triticum/chemistry , Zeatin/metabolismABSTRACT
The Spacelab-Mir-1 (SLM-1) mission is the first docking of the Space Shuttle Atlantis (STS-71) with the Orbital Station Mir in June 1995. The SLM-1 "Greenhouse-2" experiment will utilize the Russian-Bulgarian-developed plant growth unit (Svet). "Greenhouse-2" will include two plantings (1) designed to test the capability of Svet to grow a crop of Superdwarf wheat from seed to seed, and (2) to provide green plant material for post-flight analysis. Protocols, procedures, and equipment for the experiment have been developed by the US-Russian science team. "Greenhouse-2" will also provide the first orbital test of a new Svet Instrumentation System (SIS) developed by Utah State University to provide near real time data on plant environmental parameters and gas-exchange rates. SIS supplements the Svet control and monitoring system with additional sensors for substrate moisture, air temperature, IR leaf temperature, light, oxygen, pressure, humidity, and carbon-dioxide. SIS provides the capability to monitor canopy transpiration and net assimilation of the plants growing in each vegetation unit (root zone) by enclosing the canopy in separate, retractable, ventilated leaf chambers. Six times during the seed-to-seed experiment, plant samples will be collected, leaf area measured, and plant parts fixed and/or dried for ground analysis. A second planting initiated 30 days before the arrival of a U.S. Shuttle [originally planned to be STS-71] is designed to provide green material at the vegetative development stage for ground analysis. [As this paper is being edited, the experiment has been delayed until after the arrival of STS-71.]
Subject(s)
Ecological Systems, Closed , Life Support Systems/instrumentation , Spacecraft/instrumentation , Triticum/growth & development , Cell Respiration , Computer Systems , Environment, Controlled , Environmental Monitoring , International Cooperation , Plant Leaves/growth & development , Plant Leaves/metabolism , Plant Roots/growth & development , Plant Roots/metabolism , Research Design , Russia , Triticum/metabolism , United StatesABSTRACT
In cooperation with Russian colleagues, we will carry out three experiments with a super-dwarf cultivar of wheat in the plant growth chamber Svet on the Russian Space Station Mir: an early test of the root module and other instruments (July-August, 1995), a seed-to-seed experiment (1996), and a third planting that will be harvested after about 35 days, frozen, and returned to Earth for chemical analysis (1996). Plants will be photographed, sampled,and chemically fixed at intervals during the first two plantings. Instrumentation has been constructed to measure CO2, water vapor, air temperatures, infrared leaf temperatures, oxygen, pressure, irradiance levels, and moisture in the root module substrate (Balkanine). The primary objective of this equipment is to allow controllers to eliminate plant environmental stresses, leading to vigorous plant growth in microgravity. We are testing sampling and analysis techniques and growing plants in ground versions of Svet in Moscow and in Svet mockups in Utah: 12 chambers in two temperature-controlled rooms, with two compartments in each chamber (two temperatures, four CO2 concentrations, and three photoperiods in a current experiment).
Subject(s)
Ecological Systems, Closed , Life Support Systems/instrumentation , Plant Roots/growth & development , Space Flight/instrumentation , Triticum/growth & development , Weightlessness , Air Conditioning , Carbon Dioxide/analysis , Equipment Design , International Cooperation , Photoperiod , Plant Roots/physiology , Russia , Space Simulation , Temperature , Triticum/physiology , United StatesABSTRACT
Monoclonal antibodies were prepared against the plant growth regulator abscisic acid (ABA) conjugated to keyhole limpet hemocyanin through C-4. One of these antibodies was characterized for use in a competition fluorescence enzyme-linked immunosorbent assay (F-ELISA). The antibody detected femtomole quantities of ABA when used in the F-ELISA and showed minimal cross-reactivity with ABA metabolites and structural analogs. Dilution analysis suggested that the F-ELISA could be used to determine the ABA content of methanolic extracts of crude samples of wheat seeds without further purification. The F-ELISA was used to determine the effect of seed priming on ABA levels in wheat seeds. The antibody also was used in a modified noncompetitive indirect ELISA to measure ABA content of wheat caryopses. The noncompetitive ELISA was more sensitive than the F-ELISA, although the F-ELISA had a broader measuring range. When our anti-ABA antibody and a commercially available anti-ABA antibody were compared by indirect ELISA, there were no significant differences between the ABA estimates.
Subject(s)
Abscisic Acid/immunology , Antibodies, Monoclonal/immunology , Abscisic Acid/analogs & derivatives , Abscisic Acid/analysis , Abscisic Acid/metabolism , Animals , Antibodies, Monoclonal/isolation & purification , Binding, Competitive , Cross Reactions , Enzyme-Linked Immunosorbent Assay , Female , Hemocyanins/immunology , Hybridomas/immunology , Mice , Mice, Inbred BALB C , Seeds , Triticum/chemistryABSTRACT
Wheat (Triticum aestivum L., 2n = 6x = 42, AABBDD) florets were emasculated and pollinated using two apomictic wheatgrass [Elymus rectisetus (Nees in Lehm.) A. Love & Connor, 2n = 6x = 42, SSYYWW] accessions, one of which produces 2n pollen. A 2n = 42 (BII) hybrid and four 2n = 63 (B III) hybrids were obtained. The spike morphology of the B II hybrid was intermediate to that of its parents. The pollen mother cells (PMCs) of this hybrid contained on average 38.361 and 1.62 II, which was consistent with its disparate genome composition (ABDSYW). Its pollen failed to stain and no BC1 progeny was obtained. The B III hybrids (reduced egg fertilized with unreduced sperm) were grasslike and had a full complement of E. rectisetus chromosomes, the synapsis of which was slightly impaired by wheat haplome and/or cytoplasm. Their PMCs contained on average 16.30 II, 25.72 I, and 1.54 multivalents (III plus IV). Pollen stainability in these hybrids was low (<1%), and when they were used as females, one 54- and 60-chromosome BC1 were obtained. A mean of 13.25 II was observed in PMCs of the 54-chromosome BC1 and pollen stainability was 10%. Pollen stainability in the 60-chromosome BC1 was only 5%. The use of 2n-pollen-producing E. rectisetus accession accelerated hybrid and BC1 formation and may accelerate the ultimate transfer of apomixis to wheat.
ABSTRACT
Cytophotometric analyses were conducted to determine whether the DNA content of wheat callus varied by tissue culture medium or age of callus. Wheat,Triticum aestivum L. line PCYT-20, was cultured on three variations of the Murashige and Skoog (1962) growth medium. At the end of 2, 4, 6 and 8 weeks, samples were collected and prepared for Feulgen cytophotometry. Standards for the DNA measurements were readings from 100 telophase nuclei in wheat meristematic root tips. Amounts of DNA per nucleus present in telophase cells from callus grown on single-strength MS indicated that ploidy level increased 52%, 74% and 39%, respectively, over time from 2, 4, and 6 weeks as compared to the double-strength MS medium, and 29%, 60% and 32%, respectively, when coconut water was added to the single-strength MS culture medium. The shape of the mitotically-active cells in callus was more variable than in root tips cells. Callus grown on double-strength MS medium produced more shoots than callus grown on single-strength MS. Double-strength MS medium and, to a lesser extent, additional sucrose and organic nitrogen overcame the effects of 2,4-D on DNA amplification. Improved media may reduce the somaclonal variation induced by tissue culture.
ABSTRACT
The effects of O2, growth-regulators and desiccation on callus growth and somatic embryo (embryoid) development were investigated in cultures of immature embryos of two lines of Triticum aestivum L. Callus and embryoid formation were induced on media that contained N(6)-furfurylamin-opurine (kinetin) and either 2,4-dichlorophenoxyacetic acid or 3,6-dichloro-o-anisic acid, either with or without abscisic acid (ABA). Cultures containing differentiated embryoids were then exposed to high concentrations of both ABA and indole-3-acetic acid, after which samples were desiccated to approx. 10% tissue moisture. Incubating cultures in 3.2 mmol·l(-1) O2 (approx. 9%, low-O2) increased embryoid formation sixfold in one wheat line and nearly threefold in another. In the former line low-O2 caused the formation of mostly embryogenic callus. Low-O2 also decreased precocious germination of immature embryos, decreased callus growth, and improved development and viability of the resultant embryoids. Including 1.9 µmol·l(-1) ABA in the callus-induction medium reduced germination of immature embryos and reduced the incidence of embryoids with visible abnormalities. Despite the improved morphology, significantly fewer of the embryoids produced on ABA-containing medium germinated. Desiccation significantly enhanced germination of these embryoids as well as those produced on ABA-free medium.
ABSTRACT
Plant populations of Schizachyrium scoparium var. frequens with a history of long-term grazing by domestic herbivores were characterized by shorter and narrower leaf blades and tillers of lower weight than plants from populations with a history of no grazing. Following four biweekly defoliation events plants from the grazed populations additionally displayed lower specific leaf weights, lower amounts of biomass removed per tiller upon defoliation and a greater number of new and regrowing tillers. Production values per plant remained similar between the two populations because of a greater number of tillers per plant in the grazed population.A large amount of allozymic polymorphism was observed in both the grazed and non-grazed populations. Results of the electrophoretic analyses indicated that a minimum of 66% of the plants sampled represented separate genotypes. No distinction could be made between grazed and non-grazed populations in terms of allozymic partitioning. The morphological variation observed between these two populations may represent a shift in the relative dominance of a series of genotypes variously adapted to herbivory.