Influence of Drought on Graminicide Phytotoxicity in Wild Oat (Avena fatua) Grown under Different Temperature and Humidity Conditions

Controlled environmental experiments were carried out to determine the phytotoxicity of several graminicides on wild oat (Avena futua L.) as influenced by combination of drought and temperature stress or drought and low relative humidity. Compared with unstressed conditions (20/15°C plus adequate soil moisture), imazamethabenz phytotoxicity to wild oat was reduced significantly when plants were exposed to a combination of drought and high temperature (30/20°C) stress. Imazamethabenz phytotoxicity was reduced almost as much by high temperature stress alone as by a combined temperature and drought stress. When herbicides were applied to wild oat plants subjected to drought alone or to drought plus high temperature, the observed reduction in phytotoxicity from greatest to least was: fenoxaprop = diclofop > flamprop > imazamethabenz. Fenoxaprop performance was most inhibited by the combination of drought plus high temperature, although drought alone and to a lesser degree, high temperature alone, inhibited fenoxaprop action. High temperature had an adverse effect on the efficacy of fenoxaprop at lower application rates. Raising fenoxaprop application rates to 400 g ha⁻¹ overcame the inhibition caused by high temperature alone but only partially alleviated the effect of drought combined with high temperature. When plants were grown under a low temperature regimen the imposition of drought stress had little effect on imazamethabenz phytotoxicity but did reduce fenoxaprop phytotoxicity. At 25/15°C drought reduced the phytotoxicity of fenoxaprop and diclofop greatly but had no significant impact on the performance of any of the herbicides examined, regardless of soil moisture regimen. Received April 14, 1997; accepted September 22, 1997     

Effect of ammonium sulfate on the phytotoxicity, foliar uptake, and translocation of imazamethabenz in wild oat

Experiments were conducted in greenhouse, growth chamber, and laboratory conditions to determine the effect of ammonium sulfate [(NH₄)₂SO₄] on the phytotoxicity, foliar uptake, and translocation of imazamethabenz on wild oat. Rates of (NH₄)₂SO₄ up to 5% (w/v) applied with a greenhouse sprayer did not affect the phytotoxicity of the herbicide when the mix was applied at the one- to two-leaf stage. However, inclusion of 1 and 2% (NH₄)₂SO₄ increased the phytotoxicity of the herbicide when the mix was sprayed at the two- to three-leaf, or the three- to four-leaf stage. At 10%, (NH₄)₂SO₄ decreased the phytotoxicity of the sublethal dosage of the herbicide. When the herbicide was applied as individual drops to the growth chamber-grown plants, inclusion of (NH₄)₂SO₄ at 1% did not affect phytotoxicity as measured by shoot growth. The presence of (NH₄)₂SO₄ did not affect the amount of imazamethabenz retained by wild oat foliage, but it decreased [¹⁴C]imazamethabenz absorption, slightly antagonized acropetal translocation, and increased the basipetal translocation of [¹⁴C]imazamethabenz. It was concluded that application methods greatly modify the effect of (NH₄)₂SO₄ on imazamethabenz phytotoxicity. Herbicide absorption and translocation as determined by one method do not necessarily represent the absorption and translocation patterns when different application methods are used. Absorption and translocation were not the factors that were responsible for the observed effect of (NH₄)₂SO₄ on the herbicide phytotoxicity.Abbreviations SC suspension concentrate     

Tillers Do Not Influence Phytotoxicity of Imazamethabenz in Wild Oat (Avena fatua)

The response of wild oat to imazamethabenz varies with the growth stage, but the role of tillers in this regard is unclear. Removal of tillers at the three-leaf stage before spraying with imazamethabenz did not significantly affect the total shoot fresh weight measured 3 weeks later. The leaf area and dry weight of intact plants at the three-leaf stage were 17–21% greater than for plants with coleoptilar and first leaf main shoot tillers (T0 and T1) removed. The greater leaf area may have increased herbicide interception per plant. Similar fresh weight reductions in main shoot, total tillers, and total shoots were found whether imazamethabenz was applied to the plant at the two-leaf without tillers or the three-leaf with two tillers stage. Imazamethabenz applied only to the main shoot reduced total shoot dry weight more than an equivalent amount of imazamethabenz applied only to tiller T1 or applied over the whole shoot. Imazamethabenz had the least inhibitory effect on whole plant growth when applied only to T1. When ¹⁴C-herbicide was applied to the first main shoot leaf of plants at the three-leaf stage with two tillers, the ¹⁴C translocated 38% to roots, 33% to the main shoot, and nearly 30% to all tillers. When ¹⁴C-herbicide was applied to the first leaf of T1 then the ¹⁴C translocated 50% to T1, 25% to the main shoot, 20% to roots, and 5% to all other tillers. The translocation pattern and fresh weight values suggested that the presence of early tillers during herbicide application neither increased nor decreased imazamethabenz efficacy in wild oat. Received June 4, 1997; accepted June 5, 1997     

Influence of nutrient supply and plant growth regulators on phytotoxicity of imazamethabenz in wild oat (Avena fatua L.)

The influences of nutrient supply and plant growth regulators on the phytotoxicity of imazamethabenz in wild oat (Avena fatua L.) were evaluated in the greenhouse. Wild oat plants supplied with half-strength rather than one-eighth-strength Hoagland solution were more susceptible to imazamethabenz, showing greater growth reduction in main shoot and tillers. The improved herbicide efficacy at higher nutrient levels appeared related to increased herbicide interception by the greater leaf surface available. Leaves developing at either nutrient level did not differ significantly in epicuticular wax, so differential absorption appeared unlikely. Wild oat plants supplemented with nutrient, switching from low to high levels at the time of herbicide application, were as susceptible to imazamethabenz or even more so than plants growing with a constant high level of nutrition. The wild oat pure-line Montana 73, a strongly tillering line, was more susceptible to imazamethabenz than the limited-tillering line, Crop Science 40. Both 2,4-D and GA₃ reduced imazamethabenz-induced tillering. Imazamethabenz efficacy was increased by GA₃ but not by 2,4-D. These results support the hypothesis that lowering apical dominance of wild oat increases imazamethabenz activity in tillers, and that increased tillering following sublethal doses of imazamethabenz treatment is associated with the release of apical dominance.     

Effect of decapitation on absorption,translocation, and phytotoxicity of imazamethabenz in wild oat (Avena fatua L.)

The release of apical dominance by the physical destruction in situ of the apical meristem and associated leaf primordia (decapitation) promoted the growth of tillers in non-herbicide-treated wild oat plants, as indicated by increased tiller lengths and fresh weights. At 96 h after [¹⁴C] herbicide treatment following decapitation, the absorption of [¹⁴C]imazamethabenz and total translocation of radioactivity were respectively increased by 28% and 49%. By 96 h after [¹⁴C]imazamethabenz application, the radioactivity detected in the roots of decapitated plants was 45% higher than that in the roots of nondecapitated plants while the radioactivity in tillers of decapitated plants was 2.6-fold that in tillers of intact plants. Decapitation together with foliar spraying of imazamethabenz at 200 g ha^–1 further reduced tiller fresh weight, greatly decreased the total tiller number, and thereafter significantly increased overall phytotoxicity by 32% as measured by total shoot fresh weight. The results of this study support the hypothesis that main shoot apical dominance limits translocation of applied imazamethabenz to lateral shoots, rendering tillers less susceptible to growth inhibition by the herbicide.     

Reduced leaching of the herbicide MCPA after bioaugmentation with a formulated and stored Sphingobium sp.

The use of pesticides on sandy soils and on many non-agricultural areas entails a potentially high risk of water contamination. This study examined leaching of the herbicide 4-chloro-2-methylphenoxyacetic acid (MCPA) after bioaugmentation in sand with differently formulated and stored Sphingobium sp. T51 and at different soil moisture contents. Dry formulations of Sphingobium sp. T51 were achieved by either freeze drying or fluidised bed drying, with high initial cell viability of 67–85 %. Storage stability of T51 cells was related to formulation excipient/carrier and storage conditions. Bacterial viability in the fluidised bed-dried formulations stored at 25 °C under non-vacuum conditions was poor, with losses of at least 97 % within a month. The freeze-dried formulations could be stored substantially longer, with cell survival rates of 50 %, after 6 months of storage at the same temperature under partial vacuum. Formulated and long-term stored Sphingobium cells maintained their MCPA degradation efficacy and reduced MCPA leaching as efficiently as freshly cultivated cells, by at least 73 % when equal amounts of viable cells were used. The importance of soil moisture for practical field bioaugmentation techniques is discussed.     

The effect of heat waves,elevated [CO2] and low soil water availability on northern red oak (Quercus rubra L.) seedlings

The frequency and intensity of heat waves are predicted to increase. This study investigates whether heat waves would have the same impact as a constant increase in temperature with the same heat sum, and whether there would be any interactive effects of elevated [CO₂] and soil moisture content. We grew Quercus rubra seedlings in treatment chambers maintained at either ambient or elevated [CO₂] (380 or 700 μmol CO₂ mol^?1) with temperature treatments of ambient, ambient +3 °C, moderate heat wave (+6 °C every other week) or severe heat wave (+12 °C every fourth week) temperatures. Averaged over a 4‐week period, and the entire growing season, the three elevated temperature treatments had the same average temperature and heat sum. Half the seedlings were watered to a soil water content near field capacity, half to about 50% of this value. Foliar gas exchange measurements were performed morning and afternoon (9:00 and 15:00 hours) before, during and after an applied heat wave in August 2010. Biomass accumulation was measured after five heat wave cycles. Under ambient [CO₂] and well‐watered conditions, biomass accumulation was highest in the +3 °C treatment, intermediate in the +6 °C heat wave and lowest in the +12 °C heat wave treatment. This response was mitigated by elevated [CO₂]. Low soil moisture significantly decreased net photosynthesis (A_net) and biomass in all [CO₂] and temperature treatments. The +12 °C heat wave reduced afternoon A_net by 23% in ambient [CO₂]. Although this reduction was relatively greater under elevated [CO₂], A_net values during this heat wave were still 34% higher than under ambient [CO₂]. We concluded that heat waves affected biomass growth differently than the same amount of heat applied uniformly over the growing season, and that the plant response to heat waves also depends on [CO₂] and soil moisture conditions.     

Influence of temperature and light intensity on absorption, translocation, and phytotoxicity of fenoxaprop-ethyl and imazamethabenz-methyl in Avena fatua

The absorption and translocation of fenoxaprop-ethyl and imazamethabenz-methyl were investigated in wild oat (Avena fatua L.) plants grown under different temperature and light intensity conditions by using ¹⁴C tracer techniques. The phytotoxicity of both herbicides, applied as individual droplets, was also determined under similar environments. The absorption of fenoxaprop-ethyl and imazamethabenz-methyl was increased by high temperature (30/20°C) and to a lesser extent by 70% shading; low temperature (10/5°C) had limited effect on the absorption. The basipetal translocation of fenoxaprop-ethyl was not affected by high temperature, and the increase in imazamethabenz-methyl translocation at high temperature was likely the result of the increased absorption. Low temperature decreased total translocation and translocation efficiency in both fenoxaprop-ethyl and imazamethabenz-methyl. Low light intensity tended to reduce the efficiency of basipetal translocation of both herbicides. Fenoxaprop-ethyl phytotoxicity was reduced by high temperature but not by low temperature. Temperature had little effect on imazamethabenz-methyl effectiveness. Under 70% shading, the phytotoxicity of both herbicides was enhanced.Abbreviation S.E.D. standard errors of difference     

Indole-3-Acetic Acid Control on Acidic Oat Cell Wall Peroxidases

Incubation of oat coleoptile segments with 40 μm indoleacetic acid (IAA) induced a decrease of 35–60% in peroxidase activity at the cell wall compartment. Treatment with IAA also produced a similar decrease in the oxidation of NADH and IAA at the cell wall. Isoelectric focusing of ionic, covalent, and intercellular wall peroxidase fractions showed that acidic isoforms (pI 4.0–5.5) were reduced preferentially by IAA treatment. Marked differences were found between acidic and basic wall isoperoxidases in relation to their efficacy in the oxidation of IAA. A peroxidase fraction containing acidic isoforms oxidized IAA with a V _max/s_0.5 value of 2.4 × 10⁻² min⁻¹· g fw⁻¹, 4.0 times higher than that obtained for basic peroxidase isoforms (0.6 × 10⁻² min⁻¹· g fw⁻¹). In contrast, basic isoforms were more efficient than acidic isoperoxidases in the oxidation of coniferyl alcohol or ferulic acid with H₂O₂ (5.6 and 2.1 times, respectively). The levels of diferulate and lignin in the walls of oat coleoptile segments were not altered by treatment with IAA. The decrease in cell wall peroxidase activity by IAA was related more to reduced oxidative degradation of the hormone than to covalent cell wall cross-linking. Received November 1, 1998; accepted December 14, 1998     

Effect of surfactants and oils on the phytotoxicity of difenzoquat to Avena fatua, barley and wheat

Controlled drop (CDA) and conventional applications of difenzoquat to pot-grown Avena fatua were compared. With the recommended surfactant (0.5% v/v Agral), very low volume CDA was less effective than conventional spray application. However, addition of extra Agral or various blends of paraffinic oil with Agral and the surfactants Burtemul A2 or Burtemul P2 improved the effects of the CDA treatments. When difenzoquat was absent the additives were inactive against A. fatua. They had little direct effect on wheat and barley and did not substantially increase the phytotoxicity of difenzoquat to these crops. Oil/surfactant mixtures were less viscous than high concentrations of Agral, and so easier to spray. In a pot experiment, smaller (150 μm diameter) drops of difenzoquat solution were more active against A. fatua than larger (200 μm-300 μm) drops. Reduction of the spray volume within the range 40 litres/ha to 5 litres/ha also reduced phytotoxicity. An oil/surfactant additive improved the activity of all difenzoquat CDA treatments. There was slightly more effect at the lowest spray volume but interactions between additive and application treatments were not statistically significant. When simulated rain treatments were applied 2 h or 5 h after spraying, difenzoquat controlled drop application was much less phytotoxic than a conventional 150 litres/ha treatment. However, addition of an oil/surfactant mixture markedly improved the performance of CDA. When rain was withheld for 24 h the additive had relatively less effect. In the field an oil/surfactant mixture improved control of A. fatua by difenzoquat with both conventional and controlled drop treatments. The additive did not increase injury to the wheat crop. The oil/surfactant mixtures markedly improved the spreading and wetting properties of sprays. This reduced localised contact injury, which, it is suggested, improved uptake and translocation of difenzoquat.     

Activity of Triclopyr Herbicide Enhanced by Combination with Cobalt Chloride or Ammonium Nitrate

Cobalt chloride at a rate of 16 oz/acre when combined with the auxin herbicide triclopyr at 1 oz/acre synergistically enhanced the activity of the herbicide. A similar response was elicited by the addition of ammonium nitrate. Mg²⁺ or Mn²⁺ was antagonistic. The enhancement of activity by Co²⁺ or NH⁺ ₄ appeared not to be the result of a simple enhancement of triclopyr uptake by the cations. Triclopyr uptake, as determined by gas chromatography/microwave-induced plasma/chemical reaction interface mass spectroscopy, was unaffected by the cation additions. Received March 31, 1997; accepted March 24, 1998     

The transformation of nitrogen and carbon in the soil during humification of straw labelled with N15

Summary Laboratory tests were made on the effect of NaNO₃ or (NH₄)₂CO₃ on the dynamics of humification in the soil of oat straw tagged with N¹⁵. The mixture was incubated for 112 days, at constant temperature and moisture conditions. It was found that NH₄-N accelerated the straw humifications more than NO₃-N. Humification started directly after the straw was introduced into the soil. N¹⁵ derived from straw consituted a part of the forming humic compounds. Already after 14 days of incubation, the N¹⁵ of straw was found in all fractions of humic compounds. Mineralization accompanied humification. The added inorganic-N accelerated not only straw humification, but also the mineralization of forming humic compounds. This is why the added inorganic-N had no influence on the content of humic compounds. The decisive factor in the increase of humic and fulvic acids in the soil, was the straw. The inorganic N added to the straw, had no influence on the quality of humic acids formed in the soil.     

Stomatal diffusion resistances and leaf growth during droughting of Lolium perenne plants selected for contrasting epidermal ridging

Groups of Lolium perenne plants selected for either deep or shallow adaxial epidermal ridging were grown in a 16 h day of 70 W m^-2 at 25°C, and either watered daily to 33% or allowed to dry to and then watered daily to 21% or to 16% soil moisture. During a 9 day experimental period, adaxial leaf resistances (r₁) were measured with a diffusion porometer four times daily, transpiration was estimated gravimetrically, and daily rates of leaf extension were recorded. Measurements were also made of minimum abaxial resistances, stomatal frequencies and lengths, and relative leaf water content (RLWC). At 33%, 21% or 16% soil moisture, leaf extension rates of deep ridged leaves were, respectively, slower, the same, and more rapid than those with shallow ridges. At 21% or 16% soil moisture, the adaxial r_l of deep-ridged was much lower than that of shallow-ridged leaves at all four sampling times. This difference was most marked on leaves below the youngest fully expanded, and was observed among older leaves even when plants were well watered. At low RLWC (< 85%), leaf resistance was greatest in leaves with shallow ridges. There was no significant difference between the leaf types in the calculated contributions of stomatal frequency or of morphology at any one pore opening, to r_l but deep-ridged leaves had more stomataonthe abaxial surface. Daily rate of plant water loss was directly correlated (r=+ 0.86, P < 0.01) with mean daily maximum stomatal conductance (1/r_l), and rate of leaf extension negatively with maximum r_l. It is suggested that stomata operating in the concavity formed by deep ridges open wider and are less responsive to internal changes in, for example, leaf water status, than those on shallow-ridged leaves because of a more humid microenvironment at the epidermal surface. The results are discussed in relation to the concept of ‘water-savers’ and ‘water-spenders’ and its application to breeding for dry conditions.     

Thermomorphogenic and Photomorphogenic Control of Stem Elongation in Fuchsia Is Not Mediated by Changes in Responsiveness to Gibberellins

Stem elongation in Fuchsia × hybrida was influenced by cultivation at different day and night temperatures or in different light qualities. Internode elongation of plants grown at a day (25°C) to night (15°C) temperature difference (DIF+10) in white light was almost twofold that of plants grown at the opposite temperature regime (DIF−10). Orange light resulted in a threefold stimulation of internode elongation compared with white light DIF−10. Surprisingly, internode elongation in orange light was similar for plants grown at DIF−10 and DIF+10. Flower development was accelerated at DIF−10 compared with DIF+10 in both white and orange light. To examine whether the effects of DIF and light quality on shoot elongation were related to changes in gibberellin metabolism or plant sensitivity to gibberellins (GAs), the stem elongation responses of paclobutrazol-treated plants to applied gibberellins were determined. In the absence of applied gibberellins paclobutrazol (>0.32 μmol plant⁻¹) strongly retarded shoot elongation. This inhibition was nullified by the application of about 10–32 nmol of GA₁, GA₄, GA₉, GA₁₅, GA₁₉, GA₂₀, GA₂₄, or GA₄₄. The results are discussed in relation to possible effects of DIF and light quality on endogenous gibberellin levels and gibberellin sensitivity of fuchsia and their effects on stem elongation. Received October 4, 1997; accepted December 17, 1997     

Arbuscular mycorrhizal symbiosis and nonhydraulic signaling of soil drying in Vigna unguiculata (L.) Walp.

 We examined the influence of Glomus intraradices on nonhydraulic signaling of soil drying, in a drought-avoiding plant having stomates that are extremely sensitive to changes in soil moisture. Cowpea [Vigna un guiculata (L.) Walp. 'White Acre'] seedlings were grown in a greenhouse with root systems split between two pots. The 2×3×2 experimental design included two levels of mycorrhizal colonization (presence or absence of Glomus intraradices Schenck & Smith UT143), three levels of phosphorus fertilization within each mycorrhizal treatment and two levels of water (both pots watered or one pot watered, one pot allowed to dry). Stomatal conductance was mostly similar in fully watered mycorrhizal and nonmycorrhizal controls. However, g _s of half-dried, nonmycorrhizal plants was reduced on fewer days and to a lesser extent than g _s of half-dried, mycorrhizal plants, perhaps related to quicker soil drying in mycorrhizal pots. The partial soil drying treatment had little effect on leaf relative water content or osmotic potential, indicating that declines in g _s and leaf growth were induced by some nonhydraulic factor. Leaf growth was inhibited only in nonmycorrhizal plants, evidently due to a difference in phosphorus nutrition between mycorrhizal and nonmycorrhizal plants. The mycorrhizal effect on g _s was not associated with phosphorus nutrition. Inhibition of g _s was directly related to extent of soil drying, while inhibition of leaf growth was inversely related to extent of soil drying. Accepted: 4 August 1995     

Permeability of Boric Acid Across Lipid Bilayers and Factors Affecting It

Boron enters plant roots as undissociated boric acid (H₃BO₃). Significant differences in B uptake are frequently observed even when plants are grown under identical conditions. It has been theorized that these differences reflect species differences in permeability coefficient of H₃BO₃ across plasma membrane. The permeability coefficient of boric acid however, has not been experimentally determined across any artificial or plant membrane. In the experiments described here the permeability coefficient of boric acid in liposomes made of phosphatidylcholine was 4.9 × 10⁻⁶ cm sec⁻¹, which is in good agreement with the theoretical value. The permeability coefficient varied from 7 × 10⁻⁶ to 9.5 × 10⁻⁹ cm sec⁻¹ with changes in sterols (cholesterol), the type of phospholipid head group, the length of the fatty acyl chain, and the pH of the medium. In this study we also used Arabidopsis thaliana mutants which differ in lipid composition to study the effect of lipid composition on B uptake. The chs1-1 mutant which has lower proportion of sterols shows 30% higher B uptake compared with the wild type, while the act1-1 mutant which has an increased percentage of longer fatty acids, exhibited 35% lower uptake than the wild type. Lipid composition changes in each of the remaining mutants influenced B uptake to various extents. These data suggest that lipid composition of the plasma membrane can affect total B uptake. Received: 15 October 1999/Revised: 11 February 2000     

N-Carbamoyl Amino Acid Solid–Gas Nitrosation by NO/NO x : A New Route to Oligopeptides via α-Amino Acid N-Carboxyanhydride. Prebiotic Implications

α-N-Carbamoyl amino acid (CAA), whose conditions of formation in a prebiotic hydrosphere have been described previously (Taillades et al. 1998), could have been an important intermediate in prebiotic peptide synthesis through reaction with atmospheric NO _x . Nitrosation of solid CAA (glycine or valine derivative) by a 4/1 NO/O₂ gaseous mixture (1 atm) yields N-carboxyanhydride (NCA) quantitatively in less than 1 h at room temperature. The crude solid NCA undergoes quantitative oligomerization (from trimer to nonamer under the conditions we used) when treated with a (bi)carbonate aqueous buffer at pH 9. We therefore suggest that part of the prebiotic amino acid activation/polymerization process may have taken place in a dry phase (``drying-lagoon' scenario). Received: 23 June 1998 / Accepted: 7 December 1998     

Exogenous Jasmonic and Abscisic Acids Act Differentially in Elongating Tissues from Oat Stem Segments

Segments can be cut from the peducular-1 internode of oat (Avena sativa L.) shoots so as to contain the graviresponsive, auxin-sensitive leaf sheath pulvinus, and the gibberellin-sensitive internodal tissue. These two growth-capable tissues were used to study the effects and interactions of jasmonic acid (JA) and abscisic acid (ABA) in regulating cell elongation. When supplied alone at physiologic concentrations (10⁻⁵, 10⁻⁴ m), JA promoted growth and cell wall synthesis in the internodal tissue, whereas by itself, ABA inhibited internodal elongation and even inhibited JA-promoted growth. When gibberellic acid (GA₃) was used to stimulate internodal elongation, JA and ABA caused similar levels of inhibition and, at certain concentrations, were synergistic. Inhibition by ABA was initiated several hours earlier than inhibition by JA, and only the ABA effect could be partially overcome by 10⁻³ m aminoethoxyvinylglycine. Both JA and ABA inhibited elongation of pulvinar tissue that was induced to grow by gravistimulus or auxin, although here JA was more potent than ABA at equimolar concentrations. When 10⁻⁵ m fusicoccin was used as a general nonphysiologic growth stimulus, JA had no effect on the internode but inhibited the pulvinus, whereas ABA had no effect on the pulvinus but inhibited the internode. These results provide strong physiologic evidence that JA and ABA act by different mechanisms in the regulation of elongation, at least in this representative grass. Received May 28, 1996; accepted November 7, 1996     

Effects of Ring D-Modified Gibberellins on Gibberellin Levels and Development in Selected Sorghum bicolor Maturity Genotypes

Plants of early flowering mutant and wild type genotypes of Sorghum bicolor were treated with ring D-modified gibberellins (GAs), and the effects on endogenous GA levels were determined. The growth and timing of floral initiation in 58M plants grown under 18-h days (which significantly delays floral initiation in this short day plant) following treatment with these compounds, relative to GA₃ and GA₅ treatments, were also investigated. Application of the endo-isomer of C16,17-dihydro-GA₅ (endo-DiHGA₅), the exo-isomer of C16,17-dihydro-GA₅ (exo-DiHGA₅), and C16α,17-dichloromethanodihydro-GA₅ (DMDGA₅) altered GA levels in both genotypes. Each ring D-modified GA significantly inhibited shoot growth while significantly decreasing levels of GA₁ and increasing levels of its immediate precursor, GA₂₀. Gibberellin A₈ levels also decreased. Tillering was not affected by any treatment. For the early flowering genotype 58M, grown under noninductive long days, both dihydro-GA₅ isomers promoted floral initiation while shoot growth was strongly inhibited, and floral development was strongly advanced beyond floral stage 4. Gibberellin A₃ and GA₅, applied under the same conditions, promoted shoot growth slightly and gave ``floral-like' apical meristems that did not develop past floral stage 1. These results suggest that the reduced shoot growth of sorghum, which follows application of those ring D-modified GAs, is due to their inhibiting the 3β hydroxylation of GA₂₀ to GA₁, thereby reducing the GA₁ content. That floral initiation was hastened and floral development promoted in genotype 58M by application of both isomers of DiHGA₅ are in contrast to the effects of other GA biosynthesis inhibitors, which act earlier in the GA biosynthesis pathway, but are consistent with results seen for long day grasses. This suggests that endo-DiHGA₅ and exo-DiHGA₅ may be acting directly in promoting floral initiation and subsequent floral apex development of this short day plant under long day conditions. Received October 3, 1996; accepted January 22, 1997     

A genetic model and molecular markers for wild oat (Avena fatua L.) seed dormancy

Seed dormancy allows weed seeds to persist in agricultural soils. Wild oat (Avena fatua L.) is a major weed of cereal grains and expresses a range of seed dormancy phenotypes. Genetic analysis of wild oat dormancy has been complicated by the difficulty of phenotypic classification in segregating populations. Therefore, little is known about the nature of the genes that regulate dormancy in wild oat. The objectives of our studies were to develop methods to classify the germination responses of segregating wild oat populations and to find molecular markers linked to quantitative trait loci (QTL) that regulate seed dormancy in wild oat. RAPD markers OPX-06 and OPT-04 explained 12.6% and 6.8% respectively, of the F₂ phenotypic variance. OPF-17 was not significant in a simple regression model, but it was linked in repulsion to OPT-04. A three-locus model of seed dormancy in wild oat is presented based on the 41-day germination profiles of F₁, F₂, F₃, BC₁P₁F₁, BC₁P₁F₂, and BC₁P₂F₁ generations, and the 113 day germination profile of 126 F₇ recombinant inbred lines. Loci G ₁ and G ₂ promote early germination, and the D locus promotes late germination. If at least one copy of the dominant G ₁ or G ₂ alleles are present regardless of the genotype at D locus, then the individual will be nondormant. If the genotype is g ₁ g ₁ g ₂ g ₂ D_, then the phenotype will be dormant. Received: 1 December 1998 / Accepted: 1 February 1999