Wild oat is a long-standing weed problem in Australian grain cropping systems, potentially reducing the yield and quality of winter grain crops significantly. The effective management of wild oat requires an integrated approach comprising diverse control techniques that suit specific crops and cropping situations. This research aimed to construct and validate a bioeconomic model that enables the simulation and integration of weed control technologies for wild oat in grain production systems. The Avena spp. integrated management (AIM) model was developed with a simple interface to provide outputs of biological and economic data (crop yields, weed control costs, emerged weeds, weed seedbank, gross margins) on wild oat management data in a cropping rotation. Uniquely, AIM was validated against real-world data on wild oat management in a wheat and sorghum cropping rotation, where the model was able to reproduce the patterns of wild oat population changes as influenced by weed control and agronomic practices. Correlation coefficients for 12 comparison scenarios ranged between 0.55 and 0.96. With accurate parameterization, AIM is thus able to make useful predictions of the effectiveness of individual and integrated weed management tactics for wild oat control in grain cropping systems.

Herbicide resistance, documented in many economically damaging weed species, is a major threat to global crop production. The injudicious use of herbicides, often in the absence of diverse weed control strategies, poses an immense selection pressure on weed communities for resistance evolution and weed adaptive traits such as high seed dormancy. This study evaluates the interaction among developing herbicide resistance, seed size, and seed dormancy of ripgut brome (Bromus diandrus Roth), wild oat (Avena fatua L.), and hare barley [Hordeum leporinum Link; syn. Hordeum murinum L. ssp. leporinum (Link) Arcang.] collected from within intensively managed fields (in-crop) in comparison with populations in surrounding ruderal (non-crop disturbed) areas with no history of exposure to herbicides within the Western Australian grainbelt. Seed size of the three species varied by farming system (continuous cereal-intensive annual crops, diverse annual crops, pasture based) and habitat (in-crop, ruderal). Field populations of H. leporinum and B. diandrus tended to have greater seed size compared with ruderal populations. Larger seeds had significantly more dormancy in all three weed species. Field-collected populations that were exposed to herbicide applications for at least the past 5 yr exhibited significantly greater seed dormancy compared with their counterparts present in ruderal areas within the same geographic area. The association between increased seed dormancy and developing multiple herbicide resistance further complicates effective weed management.

Wild oat is a herbicide resistance-prone global weed species that causes significant economic losses in dryland and horticultural agriculture. As a result, there has been a significant research effort to control this species. A major impediment to this research is the seed coat-mediated dormancy of wild oat, which requires a labor-intensive incision or puncturing of the seed coat to initiate seed germination. This study defines the most efficient settings of a mechanical thresher to overcome wild oat seed dormancy and then validates these settings using multiple populations collected from the Western Australian grain belt. We also compare the effects of rapid mechanical scarification and known germination stimulus tactics such as scarification with sulfuric acid (H2SO4), partial endosperm removal, sandpaper scarification of the seed coat, and immersion in sodium nitroprusside (NO donor SNP) solution on wild oat seedling growth rate. Threshing treatment of 1,500 rpm for 5 s provides equivalent germination compared with manually puncturing individual wild oat seeds, with no difference in seedling relative growth rate. The mechanical scarification of seeds using the thresher resulted in greater germination (66%) than H2SO4 scarification (0%), partial endosperm removal (10%), sandpaper seed coat scarification (25%), and exposure to NO donor SNP (34%). This study demonstrates that the physical dormancy of wild oat can be rapidly overcome using a commercially available mechanical thresher.

The objective of this paper was to review the reproductive biology, herbicide-resistant (HR) biotypes, pollen-mediated gene flow (PMGF), and potential for transfer of alleles from HR to herbicide-susceptible grass weeds including barnyardgrass, creeping bentgrass, Italian ryegrass, johnsongrass, rigid (annual) ryegrass, and wild oats. The widespread occurrence of HR grass weeds is at least partly due to PMGF, particularly in obligate outcrossing species such as rigid ryegrass. Creeping bentgrass, a wind-pollinated turfgrass species, can efficiently disseminate herbicide resistance alleles via PMGF and movement of seeds and stolons. The genus Agrostis contains about 200 species, many of which are sexually compatible and produce naturally occurring hybrids and hybrids with species in the genus Polypogon. The self-incompatibility, extremely high outcrossing rate, and wind pollination in Italian ryegrass clearly point to PMGF as a major mechanism by which herbicide resistance alleles can spread across agricultural landscapes, resulting in abundant genetic variation within populations and low genetic differentiation among populations. Italian ryegrass can readily hybridize with perennial ryegrass and rigid ryegrass due to their similarity in chromosome numbers (2n = 14), resulting in interspecific gene exchange. Johnsongrass, barnyardgrass, and wild oats are self-pollinated species, so the potential for PMGF is relatively low and limited to short distances; however, seeds can easily shatter upon maturity before crop harvest, leading to wider dispersal. The occurrence of PMGF in reviewed grass weed species, even at a low rate, is greater than that of spontaneous mutations conferring herbicide resistance in weeds and thus can contribute to the spread of herbicide resistance alleles. This review indicates that the transfer of herbicide resistance alleles occurs under field conditions at varying levels depending on the grass weed species.

While climate change mainly applies to global warming and subsequent drought periods, freezing periods also are changing and may trigger genetic adaptation. However, there are few prospective, experimental demonstrations. This paper investigates how effectively genetic frost-resistant variants can respond differently to frost periods, especially in farmers’ fields where various other selection pressures occur. An experiment using Avena fatua variants was set up in the field over 8 years of winter crop rotation. The frequency of each variant identified by their leaf isozymes was estimated every year. Six years were necessary to observe a weak trend towards an increased frequency of the frost-resistant phenotype, while the other variants had apparent erratic behaviour. Selection of the frost-resistant variant was challenged by irregular low temperature selection pressure, differential dormancy, germination and seed production, and possibly herbicide sensitivity that mitigated the expression of the selection response. This experiment shows how plant polymorphism and farmers’ practices that superimpose habitat unpredictability diversify possible responses to selection pressures and delay adaptation. However, if climate change brings both higher mean temperatures and extreme values, changes of apparent plant phenology could happen for weeds species displaying the appropriate genetic variability within the time-frame of farmers’ career, thus necessitating correlative adaptation of farming practices.

Imazamethabenz is a selective herbicide used to control wild oat in small grains. The effects of rate, volume of carrier, and surfactant concentration on the efficacy of this herbicide in controlling wild oat were studied in field experiments. As each of the variables increased, wild oat control increased; the greatest degree of wild oat growth inhibition occurred at the highest herbicide rate, highest volume of carrier, and highest surfactant concentration.

AC 222,293, a postemergence herbicide for wild oat control in wheat, barley, and sunflower, was applied at five rates at three locations in Montana in the spring of 1985. Twelve and 11 crops were seeded into treated soil in 1985 and 1986, respectively. Sugarbeet, lentil, and rape were injured by residual levels of AC 222,293 14 months after application. Injury was significantly greater at one location, indicating herbicide bioavailability varied by location. Soil pH was correlated negatively with crop injury, indicating the herbicide persists longer on lower pH soils.

Field experiments were conducted from 1986 to 1988 at Lacombe and Lethbridge, Alberta and Scott, Saskatchewan to determine growth and yield response of canola to mixtures of ethametsulfuron with specific grass herbicides. Ethametsulfuron did not usually cause canola injury when mixed with sethoxydim. However, ethametsulfuron mixtures with the following grass herbicides listed in decreasing order of injury potential, often caused canola injury and yield loss: haloxyfop > fluazifop > fluazifop-P > quizalofop > quizalofop-P. Canola yield losses were severe in some experiments, ranging from 59% with quizalofop mixtures to 97% with haloxyfop mixtures; in other experiments, the same mixtures did not cause significant yield losses. ‘Tobin,’ a Brassica rapa cultivar, tended to be more susceptible to injury than the B. napus cultivars ‘Pivot’ and ‘Westar.’ Canola injury symptoms were consistent with those expected from sulfonylurea herbicides. Therefore, we suggest that specific grass herbicides differentially impair the ability of canola to metabolize ethametsulfuron to inactive forms.

Dormant line M73 wild oat caryopses were utilized to develop a system for the culture of excised embryos, to evaluate whether embryo dormancy exists, and to investigate the physiological basis for breaking dormancy. Dormant embryos cultured on N6 medium solidified with 0.25% Bacto agar displayed 70% germination in 2 d compared with approximately 20% for the other gelling agents. The non-plant-based gelling agent gellum at a concentration of 0.25% was selected for further experiments on breaking dormancy after it was determined that concentrations ≥ 0.5% decreased the rate of germination. Amending N6 medium with concentrations of 0.1 to 10 μM gibberellic acid (GA) increased the rate and extent of germination. Embryos treated with 0 to 0.01 μM GA required 6 d to attain 90% germination. Germination of dormant embryos on N6 medium without GA suggested that either true embryo dormancy did not exist in M73 or some constituent of the N6 medium promoted breaking of dormancy. Subsequent experiments indicated that the 88 mM sucrose was the constituent in the N6 medium responsible for breaking dormancy. Concentrations of sucrose from 40 to 200 mM were effective in breaking dormancy. Ten μM GA increased the rate and extent of germination of embryos cultured with 88 to 200 mM sucrose. At 88 mM, fructose, maltose, glucose, and sucrose all broke embryo dormancy. Fructose was the most active soluble sugar for breaking embryo dormancy, promoting nearly 100% germination in 4 d. As with sucrose, there was an interaction between GA and the soluble sugars in breaking dormancy. Ten μM GA with 88 mM fructose provided nearly 100% germination in 1 d. Amylose, but not amylopectin or pullulan, may substitute for soluble sugars. However, with 10 μM GA amylose, amylopectin and pullulan were equally effective in breaking dormancy. Breaking dormancy of embryos on N6 medium was independent of temperatures from 12 to 24 C in the presence of GA, but in its absence the optimum was 12 C. Application of GA to dormant caryopses significantly increased and decreased the level of glucose and sucrose, respectively, in the embryo. Gibberellic acid had a similar effect on glucose and sucrose in the endosperm tissue, except the differences were not significant at all times after treatment. The change in carbohydrate metabolism, especially in embryo tissue, may be important when considered in context with the observation that soluble sugars and GA act independently in breaking dormancy in excised M73 embryos. Breaking wild oat embryo dormancy with GA may be mainly a substitution for sugar requirement.

In growth room studies, POST applications of fenoxaprop-ethyl at 50 g ai ha−1 at the four- to five-leaf stage of development were non-toxic to barnyardgrass, large crabgrass, and yellow foxtail. POST applications of fenchlorazole-ethyl at 12.5 or 25.0 g ai ha−1 were also nontoxic to these same three species. However, when the two chemicals were applied in combination at the above rates they were toxic to all three species, indicating a synergistic interaction in all three species. In additional studies, a sensitive biotype of wild oat was severely injured by fenoxaprop-ethyl at 50 g ai ha−1 and a resistant biotype of wild oat was only slightly injured by fenoxaprop-ethyl at rates as high as 800 g ai ha−1. However, no significant interactions were observed between fenoxaprop-ethyl and fenchlorazole-ethyl in either of these wild oat biotypes.

Experiments were conducted in the field and controlled-environment chambers to determine wild oat (Avena fatua L. # AVEFA) control with difenzoquat (1,2-dimethyl-3,5-diphenyl-1H-pyrazolium) as influenced by applications at 4-h intervals during the day. Difenzoquat phytotoxicity was significantly higher in four of the six field experiments when applied at 1300 and 1700 h than at other times and was increased in the other two experiments. Difenzoquat phytotoxicity increased with temperature at treatment in the field experiments. Wild oat control was not increased by 8 h of 28 C before or after difenzoquat application compared to a constant 18 C in controlled-environment chambers. In controlled-environment chambers, wild oat control with difenzoquat was not influenced by the time of application during the day when humidity and temperature were kept constant.

The phytotoxicity of difenzoquat (1,2-dimethyl-3,5-diphenyl-1H-pyrazolium) applied to the three-leaf stages of hard red spring wheat (Triticum aestivum L. ‘Waldron’ and ‘Era’), barley (Hordeum vulgare L. ‘Beacon’) and wild oat (Avena fatua L. ♯ AVEFA) grown under constant, fluctuating, or alternating day-night temperatures was determined in controlled environment chambers. Difenzoquat injury to wild oat and Era wheat was greater at a constant 20 or 30 than at 10 C; however, injury to Waldron wheat was similar at 10, 20, and 30 C. Difenzoquat caused only slight injury to barley, and injury was similar at all temperatures. In Era wheat, selectivity of difenzoquat for wild oat was maximum with a 10-C night temperature in an otherwise 30-C-temperature environment; in Beacon barley selectivity was maximum with 3 or more days of 20- or 30-C posttreatment temperature; and in Waldron wheat selectivity was not adequate at any of the temperatures studied.

Accurate and precise estimation of weed seed bank populations is critical to studying weed seed bank demographics. Research was conducted over 3 site-years in Montana to (1) examine the spatial distribution of wild oat seed banks on a small scale (1 m2 plots), (2) compare wild oat seed bank density sample means and precision between two soil samplers, and (3) predict the sample area needed to quantify a range of wild oat seed bank densities at several levels of precision. Seed bank sample means obtained with a large sampler (10- by 10-cm box) were greater than means obtained with a small sampler (4.4- or 3.8-cm-diam cylinder) for 15 of 18 seed banks. There was no clear advantage in precision (SE/mean) when sampling seed banks using a large number of small soil samples rather than using a small number of large soil samples. Furthermore, at very low seed bank densities, using a small number of large samples gave better precision. Precision improved as sample number increased for each seed bank at each site-year. High-density seed banks tended to have better precision than low-density seed banks at any given sample number. Seed banks had an aggregated spatial distribution when sampled with either soil sampler. As the desired precision level decreases (becomes more precise), the predicted sample area required increases greatly. A seed bank containing 6,000 seeds m−2 has a predicted sample area of 0.5, 0.7, 1.3, and 2.9% of the total area to obtain precision levels of 0.5, 0.4, 0.3, and 0.2, respectively.

Yellow starthistle represents one of the most spectacular examples of biological invasion in the western United States. However, the mechanisms leading to its success have not been clearly elucidated. Although its success has been attributed to superior competitive ability, few competition studies have been performed with yellow starthistle to test this assertion. Yellow starthistle and wild oat (a dominant component of California annual grasslands) were grown in monocultures and mixtures to assess the strength of competitive interactions between them. For either species, intraspecific competition exerted a greater influence over mean plant weight than did interspecific competition. A companion study revealed temporal separation in the phenology of these plants, explaining the weak role of interspecific competition. Additional measurements of growth and soil moisture dynamics in large 270-cm-tall by 50-cm-diam polyvinyl chloride columns also showed a lack of interspecific competition and confirmed that water use patterns differed between these species, indicating niche partitioning. Wild oat reduced soil moisture to 5% but only to a depth of approximately 150 cm. Yellow starthistle depleted soil moisture to less than 5% throughout the column to a depth of at least 270 cm. These patterns were present when wild oat and yellow starthistle were grown individually or together in the columns, indicating that yellow starthistle had a greater impact on soil moisture and to greater depths. Yellow starthistle's invasion of grasslands in California does not appear to be due to superior competitive ability, but may be due to its ability to access deeper soil moisture. These results support the empty niche hypothesis that implies that invasive species are successful in new habitats because they access resources not available to resident species.

A survey conducted across agricultural ecoregions of Saskatchewan in 1996 revealed that wild oat (Avena fatua) populations resistant to acetyl-CoA carboxylase (ACCase) inhibitors were present in approximately 10% of Saskatchewan fields (2.4 million ha). In the Aspen Parkland and Boreal Transition ecoregions, this increased to 17%. The objective of this study was to determine if agronomic practices promoted or delayed resistance and to assess producer awareness of herbicide resistance. Weed resistance and management questionnaire data from the 1996 resistance survey and management questionnaire data from the 1995 Saskatchewan weed survey were submitted to multiway frequency analysis. The frequency of occurrence of herbicide-resistant wild oat was related directly to ACCase inhibitor use. Resistance to cyclohexanedione (CHD) herbicides was not related to CHD use but to frequency of ACCase inhibitor use (i.e., CHD + aryloxyphenoxypropanoate [AOPP]), suggesting that the pressure imposed by AOPPs contributed to the selection of CHD resistance in wild oat. ACCase inhibitor use was more extensive in the Aspen Parkland and Boreal Transition ecoregions than in the Mixed and Moist Mixed Grassland ecoregions. Crop rotations were not conducive to rotation of herbicides with different sites of action. Frequency of ACCase inhibitor use increased with frequency of annual crops, in spite of the inclusion of cereal and dicot crops in the rotation. Producers utilizing conservation tillage practices in the Grassland ecoregions used proportionally more ACCase inhibitors than those using conventional tillage practices. This increase in ACCase use in conservation tillage systems did not result in an increased incidence of wild oat populations resistant to ACCase inhibitors. Producers reporting troublesome wild oat populations tended to have proportionally more ACCase-resistant wild oat. Producers who reported practicing weed sanitation were less likely to have resistant wild oat than those who were less careful. Increased awareness and implementation of management practices that will reduce the dependency on ACCase herbicides are required to better enable producers to prevent, delay, or manage herbicide-resistant wild oat populations.

Empirical models of crop–weed competition are integral components of bioeconomic models, which depend on predictions of the impact of weeds on crop yields to make cost-effective weed management recommendations. Selection of the best empirical model for a specific crop–weed system is not straightforward, however. We used information–theoretic criteria to identify the model that best describes barley yield based on data from barley–wild oat competition experiments conducted at three locations in Montana over 2 yr. Each experiment consisted of a complete addition series arranged as a randomized complete block design with three replications. Barley was planted at 0, 0.5, 1, and 2 times the locally recommended seeding rate. Wild oat was planted at target infestation densities of 0, 10, 40, 160, and 400 plants m−2. Twenty-five candidate yield models were used to describe the data from each location and year using maximum likelihood estimation. Based on Akaike's Information Criterion (AIC), a second-order small-sample version of AIC (AICc), and the Bayesian Information Criterion (BIC), most data sets supported yield models with crop density (Dc), weed density (Dw), and the relative time of emergence of the two species (T) as variables, indicating that all variables affected barley yield in most locations. AIC, AICc, and BIC selected identical best models for all but one data set. In contrast, the Information Complexity criterion, ICOMP, generally selected simpler best models with fewer parameters. For data pooled over years and locations, AIC, AICc, and BIC strongly supported a single best model with variables Dc, Dw, T, and a functional form specifying both intraspecific and interspecific competition. ICOMP selected a simpler model with Dc and Dw only, and a functional form specifying interspecific, but no intraspecific, competition. The information–theoretic approach offers a rigorous, objective method for choosing crop yield and yield loss equations for bioeconomic models.

It has been proposed that gibberellic acid (GA3) promotes germination by overcoming restrictions in sugar production and utilization in afterripening-responsive dormant caryopses. While their germination rates were similar, germination commenced sooner in afterripened wild oat (Avena fatua L.) caryopses than in dormant caryopses treated with GA3 and dormant excised embryos treated with GA3 plus fructose (Fru). Limited germination occurred in dormant excised embryos cultured with GA3 alone. Carbohydrate concentrations were measured over time in dormant caryopses and excised embryos whose germination was induced with GA3 and GA3 plus Fru. The concentration of sucrose (Suc) in the endosperm declined prior to germination of dormant GA3-treated caryopses. Raffinose (Raf) family oligosaccharides in the embryos of dormant GA-treated caryopses remained relatively constant prior to and shortly after the onset of germination. In contrast, Raf family oligosaccharides in the embryos of afterripened caryopses declined prior to germination. Together this suggests Raf family oligosaccharide utilization is not associated with germination per se. Increased starch levels, which occurred in dormant excised embryos treated with Fru and GA3 plus Fru, were associated with dormancy because similar effects were not apparent in afterripened embryos cultured with Fru. An initial decline in the concentration of Raf family oligosaccharides in dormant embryos cultured with GA3 or GA3 plus Fru seems to be a result of the excision process. GA3 appears to stimulate the germination of dormant embryos by enhancing the uptake or utilization of Fru. It appears that GA3 and afterripening-induced changes in carbohydrate utilization in dormant caryopses are different.