Successful weed management, particularly use of chemical control, is very important for commercial lettuce production on organic soils in the Everglades Agricultural Area in south Florida. Field experiments were conducted in 2016 and 2017 to determine the efficacy of herbicides (pronamide, bensulide, imazethapyr, or oxyfluorfen) applied preemergence (PRE) either alone or followed by a postemergence (POST) application of imazethapyr for weed control and lettuce (romaine and iceberg) yield. Preemergence-applied oxyfluorfen (0.56 kg ha−1) resulted in significant lettuce injury, including stand loss, while PRE applications of pronamide (4.44 kg ha−1), bensulide (5.6 and 10.1 kg ha−1), or imazethapyr (0.035 g ha−1) resulted in transient lettuce injury and no significant stand loss. Similarly, PRE-applied pronamide, bensulide, and imazethapyr followed by POST-applied imazethapyr did not result in significant lettuce stand loss or injury. When contrasted as a group, PRE-applied herbicides followed by a POST application of imazethapyr provided better spiny amaranth and common lambsquarters control compared with PRE-applied herbicides or POST-applied imazethapyr-only treatments. Lettuce yield was highest with PRE herbicides followed by POST imazethapyr compared with PRE herbicides or POST-applied imazethapyr-only treatments, indicating a yield benefit of having a PRE followed by POST herbicide weed control program in lettuce grown on organic soils. However, oxyfluorfen is not an option for lettuce on organic soils because of unacceptable stand reduction and crop injury. Whether to apply pronamide, bensulide, or imazethapyr PRE followed by a POST application of imazethapyr for broadleaf weed control in lettuce on organic soils depends on the species present, cost, and ease of application.

Herbicide carrier water hardness and pH can be variable depending on the source and geographic location. Herbicide efficacy can be affected by the pH and hardness of water used for spray solution. Field and greenhouse studies were conducted to evaluate the effect of carrier water pH and hardness on premixed dicamba and glyphosate efficacy. Treatments were combinations of water pH at 4, 6.5, or 9; and water hardness at 0 (deionized water), 400, or 800 mg L−1 of CaCO3 equivalent. In the field study, dicamba and glyphosate were applied at 0.55 and 1.11 kg ae ha−1, respectively, and half of these rates were applied in the greenhouse study. There was no interaction between carrier water pH and hardness on dicamba and glyphosate efficacy; however, the main effects of carrier water pH and hardness were significant. Herbicide efficacy was reduced with carrier water at pH 9 compared with pH 4. In the field study, common lambsquarters, common ragweed, horseweed, or Palmer amaranth control was improved 6% or more at carrier water at pH 4 compared with pH 9. Similar results were observed with water pH for giant ragweed, Palmer amaranth, or pitted morningglory control in the greenhouse study. Carrier water hardness at 400 or 800 mg L−1 reduced common ragweed, giant ragweed, or horseweed control compared with 0 mg L−1. Similarly, common lambsquarters, Palmer amaranth, or pitted morningglory control was reduced at least 10% with carrier water hardness at 800 mg L−1 compared with 0 mg L−1. These results indicate carrier water at acidic pH and of no hardness is critical for dicamba and glyphosate application, and spray solution needs to be amended appropriately for an optimum efficacy.

Tall weeds escaping early weed management, such as weeds resistant to one or multiple herbicides, are an increasing concern. When weeds reach a certain size, few options other than hand weeding will limit the production and dispersal of seeds. The objective of this project was to evaluate the efficacy of the Bourquin Organic Weed Puller® (a rotating series of wheels that grab and pull) at removing tall weeds before they shed seeds in soybean and adzuki bean. Trials were set up in Canada at the Agriculture and Agri-Food Canada research farms at Saint-Jean-sur-Richelieu (SJR), QC (2 yr), and Harrow (HAR), ON (1 yr), on a loamy and a sandy soil, respectively. The experimental design included crops of different potential heights (different soybean cultivars and adzuki bean), two weed species per location (common lambsquarters [both locations] and common ragweed or redroot pigweed at HAR), and two pulling dates. The set-up also included weedy and herbicide-treated control plots. Weeds overtopping the crop canopy by at least 10 cm were tagged and characterized. Damage from the weed puller was rated as 1, pulled (desired effect); 2, cut; 3, folded; 4, stripped; and 5, intact. The seed production of damaged and intact weeds was also recorded. Less than one-third of common ragweed or redroot pigweed plants were pulled during any treatment combination. The highest pulling rates were observed for common lambsquarters at SJR (43%), but very few were pulled at HAR (3.1% max). Pulling rates were not high enough to potentially control seed inputs from herbicide-resistant populations, and successfully pulled common lambsquarters left on the ground produced thousands of viable seeds.

Previous reports have underscored antagonism that may result from mixing glyphosate and glufosinate across a wide range of application rates and for various broadleaf and grass weed species, but no investigation has been conducted to characterize glyphosate absorption and translocation when combined with glufosinate. The objectives of this study were to evaluate herbicide efficacy and assess herbicide interaction and physiological response with combinations of glyphosate and glufosinate on common lambsquarters, velvetleaf, and giant foxtail. Greenhouse studies to determine interaction resulted in strong and persistent antagonism between glyphosate at 110 and 220 g ae ha−1 and glufosinate at 20 or 40 g ae ha−1 in giant foxtail, whereas only transient and reduced antagonism was noted for velvetleaf and common lambsquarters. Combining glyphosate and glufosinate increased the maximum absorption of glyphosate by 9% and 23% in velvetleaf and giant foxtail, respectively, compared with glyphosate alone. In velvetleaf, averaged over time, only 2.6% of the applied radioactivity translocated out of the treated leaf when glufosinate was mixed with glyphosate compared with 9.9% when glyphosate was applied alone. In giant foxtail, 21.6% of the [14C]glyphosate translocated out of the treated leaf when glufosinate was mixed with glyphosate compared with 52.4% when glyphosate was applied alone. Conversely, no change in the radioactive pattern of translocation was noted for common lambsquarters. These results suggest that reduced translocation of glyphosate is the physiological mechanism responsible for the antagonism observed between glyphosate and glufosinate in giant foxtail and, to a lesser extent, in velvetleaf.

Biofumigation is practiced to control soilborne pests and weeds in agronomic fields. The objectives of this research were to assess the dose response of weed seeds to Indian mustard biofumigation and associate responses to seed dormancy state, initial dormancy, and seed parameters. A petri dish biofumigation methodology was developed to expose seeds of common lambsquarters, bird vetch, wild carrot, common ragweed, green foxtail, velvetleaf, hairy galinsoga, and red clover to allelochemicals produced after rehydrating 0 (control), 1.94, 2.90, 5.81, 11.61, and 17.41 mg cm−2 of dried mustard powder. Weed species expressed specific dose responses, estimated ED50, LD50, and maximal mortality. Hairy galinsoga and wild carrot were consistently the most affected by biofumigation, with maximal mortality reaching 97% and 95%, ED50 values for germination were 1.91 and 2.68 mg cm−2 , and LD50 values were 3.31 and 3.69 mg cm−2 of dried mustard tissue, respectively. Initial dormancy was assessed by germination and tetrazolium tests. Seed parameters such as testa thickness, relative weight of the testa, and seed size were measured directly by manual dissection, weighing seed structures, and stereomicroscopic imaging software measurements. Linear regression analyses revealed initial dormancy to be positively related to ED50 and LD50 values with a significant interaction with seed surface and seed width, respectively. Exposure to 5.81 mg cm−2 of dried mustard powder increased common ragweed seed mortality for after-ripened seeds by 293% and by 58% for primary dormant seeds compared with untreated seeds. Mortality of common lambsquarters secondary and primary dormant seeds increased by 730% and 106%, respectively, and for wild carrot by 1,193 and 156%, respectively. Results underline the potential to incorporate biofumigation into weed management programs for repression of susceptible weed species.

Field experiments were conducted in 1992 and 1993 to characterize the weed seed bank, to determine the influence of moldboard plowing and secondary soil disturbance on the emergence pattern of weeds, and to measure weed seed bank depletion by emergence in a long-term moldboard plow corn cropping system. Viable seeds of common lambsquarters, redroot pigweed, and each of 10 other species accounted for about 85, about 9, and less than 1%, respectively, of the total weed species in the seed bank. A negative binomial distribution described the spatial distribution of viable seeds of 10 species, but not of common lambsquarters or of redroot pigweed. Decreased density of seeds among species was associated with increased aggregation. Secondary soil disturbance increased the rate and magnitude of common lambs quarters emergence in 1992 but did not influence emergence in 1993. Secondary soil disturbance did not influence the magnitude and rate of emergence of redroot pigweed or velvetleaf. Whereas cumulative growing degree days from April through July were similar between years, the amount of rainfall was about 50% less in 1992 than in 1993. Secondary soil disturbance may have increased common lambsquarters emergence by increasing the availability of soil moisture and improving conditions for seed germination during the dry year. Even though seed bank depletion by seedling emergence was relatively low for all species, secondary soil disturbance in creased seed bank depletion of common lambsquarters and redroot pigweed about 7- and 3-fold, respectively, in 1992. Seasonal variation in the amount of rainfall may have influenced the effect of soil disturbance on emergence and seed bank depletion of common lambsquarters, which is the most abundant species in the weed community.

The influence of secondary soil disturbance on the emergence pattern and seed bank depletion of an annual weed community in a long-term, no-tillage corn cropping system was determined in 1992 and 1993. As a component of this research, the seed bank was characterized prior to implementation of soil disturbance treatments. The seed bank was initially composed of common lambsquarters, redroot pigweed, and giant foxtail, with approximately 55, 36, and 8% of the total viable seeds, respectively. The remaining 1% was comprised of five other species in 1992 and eight in 1993. The spatial distribution of viable seeds of each species, except common lambsquarters and redroot pigweed, was described by a negative binomial distribution. Three dispersion indices indicated that seeds of individual and total weed species were aggregated and that the level of aggregation of viable seeds of a species was associated with seed density; at lower seed densities, the level of aggregation was greater. Soil disturbance increased common lambsquarters emergence 6-fold in 1992 relative to nondisturbed soil, but did not influence emergence in 1993. Rainfall was about 50% less in 1993. In contrast, soil disturbance increased giant foxtail and redroot pigweed emergence approximately 6- and 3-fold in 1992 and 1993, respectively. Seedling emergence associated with soil disturbance, relative to nondisturbed soil, increased seed bank depletion of common lambsquarters 16-fold in 1992, and giant foxtail and redroot pigweed and average of 6- and 3-fold in 1992 and 1993, respectively. These results indicated that soil disturbance increased seedling emergence and seed bank depletion of the predominant species in the weed community of a long-term, no-tillage system, but that this response was dependent on rainfall for common lambsquarters.

Differential response of three weed species to prosulfuron was examined through studies of acetolactate synthase (ALS) sensitivity, uptake, translocation, and metabolism of the herbicide. Sensitivity of common cocklebur, common lambsquarters, and sicklepod ALS to prosulfuron was similar with I50 values of 3.3, 4.5, and 8.8 nM, respectively. Absorption of the herbicide increased with time for all three weed species. Percent absorption 2 d after application for common cocklebur, common lambsquarters, and sicklepod was 8, 33, and 26%, respectively. An average of 53% of the absorbed herbicide remained in the treated leaves of common cocklebur, 80% in common lambsquarters, and 93% in sicklepod. Approximately 33, 15, and 5% of the absorbed herbicide was translocated into the upper shoots of common cocklebur, common lambsquarters, and sicklepod, respectively. Metabolism of 14C-prosulfuron 1, 2, and 4 d after application was greater in sicklepod than in common lambsquarters or common cocklebur. The results suggest a combination of differential rates of translocation and metabolism may account for the differing sensitivity of these weeds at the whole plant level.

In a semiarid Mediterranean site in central Spain, field experiments were conducted on a Calcic Haploxeralf (noncalcic brown soil), which had been managed with three crop rotations and two tillage systems (no-tillage and conventional tillage) since 1987. The crop rotations consisted of barley→vetch, barley→sunflower, and a barley monoculture. The study took place in two growing seasons (1992–1994) to assess the effects of management practices on the weed seedbank. During this period, spring weed control was not carried out in winter crops. In the no-tillage system, there was a significant increase in the number of seeds of different weed species: anacyclus, common purslane, corn poppy, knotted hedge-parsley, mouse-ear cress, spring whitlowgrass, tumble pigweed, venus-comb, and Veronica triphyllos. Conversely, the presence of prostrate knotweed and wild radish was highest in plots under conventional tillage. These results suggest large differences in the weed seedbank as a consequence of different soil conditions among tillage systems, but also the necessity of spring weed control when a no-tillage system is used. With regard to crop rotations, the number of seeds of knotted hedge-parsley, mouse-ear cress, and spring whitlowgrass was greater in the plots under the barley→vetch rotation. Common lambsquarters dominated in the plots under the barley→sunflower rotation, whereas venus-comb was the most frequent weed in the barley monoculture. Larger and more diverse weed populations developed in the barley→vetch rotation rather than in the barley→sunflower rotation or the barley monoculture.

Greenhouse and laboratory studies were conducted to determine the effects of bentazon on the crop safety, efficacy, foliar absorption, and translocation of thifensulfuron when it is applied to soybean, velvetleaf, and common lambsquarters. A metabolism study was conducted on soybean. Thifensulfuron applied at 1.1 g ai ha−-1 with 28% urea ammonium nitrate (2.5% v/v) and BAS-0904805 (Dash) adjuvant (0.63% v/v) reduced the growth of velvetleaf and common lambsquarters by an average of 91 and 84%, respectively. The addition of 420 g ai bentazon ha−-1 had no effect on thifensulfuron efficacy in the weed species. Soybean dry weights were decreased by 58% when thifensulfuron was applied at 2.2 g ha−-1 but were decreased by only 36% when bentazon, at 420 g ha−-1, was added. In the absorption study, the addition of bentazon reduced foliar absorption of 14C-thifensulfuron into velvetleaf and common lambsquarters 8 and 24 h after treatment (HAT), but absorption into soybean was not affected. Bentazon reduced the translocation of 14C from thifensulfuron out of the treated leaves of velvetleaf and common lambsquarters by at least 16 and 11%, respectively, beyond 24 HAT. Soybean translocated 18, 29, and 26% of absorbed 14C out of the treated leaflets 24, 72, and 168 HAT, respectively. These translocation values were reduced to 7, 12, and 11%, respectively, when bentazon was tank-mixed with thifensulfuron. Soybean metabolized 35% of recovered 14C-thifensulfuron by 24 HAT. Addition of bentazon did not change this level of metabolism. These studies suggest that the physiological basis for the decrease of soybean injury from thifensulfuron, when it is tank-mixed with bentazon, is decreased thifensulfuron translocation.

Peak germination and emergence of common lambsquarters usually occur in early to mid-spring, but both processes can occur during summer and fall. Seeds produced by different common lambsquarters cohorts (seedlings that emerge at nearly the same time) may vary in dormancy status, response to environmental conditions, and response to management factors. Therefore, experiments were conducted to determine the influence of different cohorts on common lambsquarters demography. Field experiments determined plant density, biomass, and seed production of different common lambsquarters cohorts within a crop-free community of annual weed species that included redroot pigweed, giant foxtail, and velvetleaf. Common lambsquarters plant density and aboveground biomass were greater for a mid-May cohort than for early June, late June, mid-July, or early August cohorts, but seed production of the mid-May and early June cohorts did not differ (about 192,000 seeds m−2) and was greater than that of other cohorts (111,500 seeds m−2 or less). In the laboratory, percent germination prior to stratification (exposure of seeds to low temperatures) was less for seeds harvested from early May and late May cohorts (≥ 9%) than those of mid-June or early July cohorts (≤ 75%). After stratification in the field, percent emergence (seedlings per number of planted seeds) and mean emergence time were similar among early May, late May, mid-June, and early July cohort seed sources, and were not influenced by shallow burial in soil. These results suggest that recruitment from seeds produced by different common lambsquarters cohorts is similar, but proportional to the number of seeds produced by each cohort.

A better understanding of the influence of various crop and weed management practices on spatiotemporal dynamics of weeds could improve the design of integrated weed management systems. We examined the influence of 18- and 76-cm soybean row spacings on emergence pattern and spatial aggregation of giant foxtail, common lambsquarters, and velvetleaf seedling cohorts. In addition, we characterized the soil seedbank and determined the quantitative and spatial relationship between the seedbank and seedling populations. Viable seeds of about 10 weed species and twice as many species of seedlings were identified in the weed community. Giant foxtail and common lambsquarters were the predominant species in the seedling and seedbank population, respectively, each accounting for 60 to 70% of the total weed species density. Emergence of giant foxtail, common lambsquarters, and velvetleaf depleted 12 to 33%, < 2% and 12 to 49% of the seedbank in the upper 10 cm of the soil profile. Peak time and periodicity of weed emergence was not influenced by soybean row spacing, and peak time of emergence of giant foxtail, common lambsquarters, and velvetleaf occurred 3 to 4, 3 to 6, and 3 to 9 weeks after soybean planting (WAP), respectively. Magnitude of giant foxtail emergence 5, 6, and 9 WAP was 98, 96, and 76% greater in 76- than in 18-cm row soybeans only when the population of 76-cm row soybeans was 57% lower than the 18-cm soybeans in 1997. Giant foxtail and common lambsquarters seeds in the seedbank were aggregated in 1996 and 1997 according to the Taylor power law (TPL) and the negative binomial distribution (NBD). The TPL and the NBD were similar in describing the spatial aggregation of giant foxtail and common lambsquarters but not some velvetleaf seedling cohorts. The spatial aggregation of seedlings varied among cohorts for different weed species and was likely due to species-specific biological characteristics that influence seed dispersal, germination, and seedling emergence. Within a 1.5-ha area, aggregation declined with decreasing density. Within a 24-m2 area, the level of aggregation of all weed species decreased as seedling densities increased. These results indicated that soybean row spacing influenced neither weed emergence pattern nor weed spatial aggregation; thus, several management decisions can be similar in 18- and 76-cm row soybeans.

Weed seeds can require an exposure to light for induction of germination. Conducting tillage operations at night and thus preventing the photoinduction of germination has been proposed as a means to reduce weed emergence in agricultural systems. This research was conducted to evaluate night tillage as a weed management option and to determine which tillage operations have the greatest effect on light-mediated recruitment. Weed emergence was evaluated after conducting factorial combinations of day and night moldboard plowing and disking in the springtime from 1992 through 1995. The light environment during disking generally had a slightly greater effect on emergence than the light environment during plowing. Emergence of pigweed species and giant foxtail was, at most, 30 to 55% higher following day vs. night disking. Emergence of other weeds was not affected by the light environment during tillage. We conclude that night tillage may not be a viable approach to weed management due to insufficient reductions in weed emergence associated with night tillage and the high degree of variability in the recruitment response to light conditions during tillage.

Many growers perceive that reduced herbicide inputs and greater reliance on mechanical methods will result in increased weed management problems over time. Previous research has shown short-term benefits of integrated weed management strategies, but information concerning the long-term implications of these strategies is lacking. Therefore, research was conducted from 1992 through 1995 to determine the influence of full-rate preemergence broadcast, half-rate preemergence broadcast plus cultivation, and full-rate preemergence band plus cultivation treatments on weed population and seedbank dynamics in no-tillage (NT), chisel plow (CP), and moldboard plow (MP) systems in both continuous corn (CC) and corn—soybean (CS) rotation. Seventeen weed species were identified in the plant population and seedbank across all treatments, but common lambsquarters, giant foxtail, and redroot pigweed dominanted. Vertical distribution of weed seeds in soil was influenced by tillage, with 74, 59, and 43% of the total viable seed of these species less than 10 cm deep in NT, CP, and MP, respectively. In contrast, seed dormancy in the spring was not influenced greatly by tillage and averaged 79, 10, and 42% for common lambsquarters, giant foxtail, and redroot pigweed, respectively, across tillage methods. Crop rotation was not a major factor influencing weed population and seedbank dynamics. From 1992 to 1995, reduction of shoot biomass and seed production of the predominant weed species were similar among weed management treatments in most tillage and crop rotation systems. The influence of weed management treatments on the seedbank was also similar, with up to 50, 95, and 92% less seed of common lambsquarters, giant foxtail, and redroot pigweed, respectively, in the seedbank in 1995 than in 1992. Corn and soybean grain yields were similar among weed management treatments and were greater than the nontreated check in each tillage and crop rotation treatment. These results indicate that reduced herbicide inputs plus interrow cultivation were as effective as full-rate herbicide inputs for the management of several annual weed species in both conventional- and conservation-tillage systems over 4 yr.

Field experiments, conducted from 1991 to 1994, generated information on weed seedbank emergence for 22 site-years from Ohio to Colorado and Minnesota to Missouri. Early spring seedbank densities were estimated through direct extraction of viable seeds from soil cores. Emerged seedlings were recorded periodically, as were daily values for air and soil temperature, and precipitation. Percentages of weed seedbanks that emerged as seedlings were calculated from seedbank and seedling data for each species, and relationships between seedbank emergence and microclimatic variables were sought. Fifteen species were found in 3 or more site-years. Average emergence percentages (and coefficients of variation) of these species were as follows: giant foxtail, 31.2 (84%); velvetleaf, 28.2 (66); kochia, 25.7 (79); Pennsylvania smartweed, 25.1 (65); common purslane, 15.4 (135); common ragweed, 15.0 (110); green foxtail, 8.5 (72); wild proso millet, 6.6 (104); hairy nightshade, 5.2 (62); common sunflower, 5.0 (26); yellow foxtail, 3.4 (67); pigweed species, 3.3 (103); common lambsquarters, 2.7 (111); wild buckwheat, 2.5 (63), and prostrate knotweed, 0.6 (79). Variation among site-years, for some species, could be attributed to microclimate variables thought to induce secondary dormancy in spring. For example, total seasonal emergence percentage of giant foxtail was related positively to the 1st date at which average daily soil temperature at 5 to 10 cm soil depth reached 16 C. Thus, if soil warmed before mid April, secondary dormancy was induced and few seedlings emerged, whereas many seedlings emerged if soil remained cool until June.

Greenhouse and field experiments were conducted to evaluate the potential for antagonistic or synergistic interactions from tank mixtures of glyphosate plus a selective herbicide applied postemergence. In the greenhouse, glyphosate at 420 g ae ha−1 plus 28% liquid urea-ammonium nitrate (28% UAN) provided at least 89% control of common lambsquarters and common ragweed. Glyphosate at 1,680 g ha−1 plus 28% UAN provided less than 81% control of velvetleaf and less than 75% control of ivyleaf morningglory. Tank mixing bentazon at 1,120 g ai ha−1 with glyphosate at 420 g ha−1 synergistically increased control of velvetleaf. Tank mixtures of glyphosate plus a selective herbicide were predominately additive in control of common lambsquarters, common ragweed, and velvetleaf. Several tank mix combinations of chlorimuron or imazethapyr plus glyphosate plus 28% UAN were antagonistic in control of ivyleaf morningglory. In the field, glyphosate at 840 g ha−1 plus 28% UAN provided at least 88% control of common lambsquarters and velvetleaf in 1994. However, glyphosate at 840 g ha−1 plus 28% UAN provided only 60% control of velvetleaf in 1995. Tank-mixing bentazon or CGA-248757 with glyphosate at 420 g ha−1 increased velvetleaf and common lambsquarters control in 1995. In general, adding chlorimuron, imazethapyr, or thifensulfuron to glyphosate plus 28% UAN did not increase control of common lambsquarters or velvetleaf. Tank mixing imazethapyr with glyphosate plus 28% UAN antagonized velvetleaf control in 1994 and in 1995. The tank mixture of thifensulfuron at 2 g ha−1 plus glyphosate at 420 g ha−1 plus 28% UAN increased soybean injury in the field in 1994. However, tank mixing chlorimuron, imazethapyr, or thifensulfuron with glyphosate plus 28% UAN did not increase soybean injury in the greenhouse or in the field in 1995.

Field and greenhouse experiments were conducted in 1995 and 1996 to determine soybean injury and weed control differences from imazamox and imazethapyr applied postemergence with a nonionic surfactant or methylated seed oil and with selected tank mixtures. Soybean injury from imazamox at 35 g ai ha−1 plus either a methylated seed oil or nonionic surfactant was equal to injury from imazethapyr at 70 g ai ha−1 in the greenhouse and field. Imazamox provided greater common lambsquarters control than imazethapyr in the field in 1995 and in the greenhouse. Thifensulfuron tank mixed with imazethapyr increased common lambsquarters control, while soybean response increased when thifensulfuron was tank mixed with imazamox. Common ragweed dry weight was reduced 61 to 64% from 35 g ha−1 imazamox and 70 g ha−1 imazethapyr in the field; however, imazamox provided greater common ragweed control than imazethapyr in the greenhouse. Tank mixtures of lactofen with imazamox or imazethapyr increased common ragweed control and resulted in greater soybean seed yield in 1996 than when imazamox and imazethapyr were applied alone; however, lactofen antagonized giant foxtail control with imazamox and imazethapyr, and antagonized common lambsquarters control with imazamox. Giant foxtail control in the greenhouse was antagonized more when acifluorfen, fomesafen, and lactofen were tank mixed with 35 g ha−1 imazethapyr than with 35 g ha−1 imazamox. Giant foxtail control with imazamox or imazethapyr applied alone or with diphenyl ether herbicides increased when 28% urea ammonium nitrate was added with nonionic surfactant compared with nonionic surfactant only. Imazethapyr antagonized giant foxtail control by clethodim in the field and was more antagonistic than imazamox in the greenhouse. A methylated seed oil improved common ragweed control by imazethapyr at 70 g ha−1 and imazamox at 18 and 35 g ha−1, while common lambsquarters and velvetleaf control increased when a methylated seed oil was included with 18 g ha−1 imazethapyr compared to nonionic surfactant in the greenhouse.

Greenhouse and laboratory experiments were conducted to evaluate foliar absorption, translocation, and efficacy of glufosinate on four weed species. The rate of glufosinate required to reduce shoot dry weight by 50% (GR50) varied between weed species. GR50 values for giant foxtail, barnyardgrass, velvetleaf, and common lambsquarters were 69, 186, 199, and 235 g ai ha−1, respectively. Absorption of 14C-glufosinate increased with time and reached a plateau 24 hours after treatment (HAT). Absorption of 14C-glufosinate was 67, 53, 42, and 16% for giant foxtail, barnyardgrass, velvetleaf, and common lambsquarters, respectively. Translocation of absorbed 14C-glufosinate from the treated leaf was greatest for giant foxtail and barnyardgrass (15 and 14% 24 HAT of absorbed 14C-glufosinate, respectively). This compared to 5 and < 1% for translocation of absorbed 14C-glufosinate from the treated leaves of velvetleaf and common lambsquarters. The majority of 14C-glufosinate translocated by giant foxtail and barnyardgrass was found below the treated leaf and in the roots, indicating phloem mobility of the herbicide. Differential absorption and translocation of 14C-glufosinate may be contributing factors to the differential sensitivity observed between weed species.

The relative leaf area of weeds is a good predictor of the outcome of weed-crop competition. However, this variable has not been used in decision-making tools for integrated weed management because leaf area cannot be measured quickly. A powerful image analysis system for measuring leaf cover (the vertical projection of plant canopy on the ground) has been developed and validated. This research was conducted to compare the efficiency of weed relative leaf area and relative leaf cover in predicting corn yield loss. Field studies were conducted in 1996 and 1997 using varying densities of common lambsquarters, barnyardgrass, common lambsquarters plus barnyardgrass, and a natural weed community. Corn grain yield and biomass loss varied with weed infestation type and year. Values of the relative damage coefficient of weeds (q) were smaller in 1997 compared with 1996. For both years, the relative leaf area of weeds was an adequate predictor of corn yield loss (r 2 varied from 0.61 to 0.92). The precision of the predictions was not influenced by the leaf area sampling period (four- or eight-leaf stage of corn). In general, smaller values of q and m (predicted maximum yield loss) were obtained as a consequence of using the relative leaf cover of weeds in model fitting. However, percentages of variation explained by the model (from 0.67 to 0.90) were similar to values obtained with the relative leaf area. On the basis of the residual mean squares, neither of the variables could be declared superior to the other in yield loss prediction. The development of weed control decision-making tools using the relative leaf cover of weeds may require improvements prior to being used in weed management systems. Such improvements would include use of appropriate sampling and image-processing techniques, development and validation of empirical models specific to individual situations, and proper identification of the crop growth stage at which leaf cover must be assessed.

Generalizations concerning the effects of management practices on weed community dynamics often lack robustness, most likely because of the concomitant effects of agronomic and environmental factors. However, such generalizations, when valid, provide useful grounds for predictions and are thus desirable. This study attempted to evaluate the relative importance of crop rotation, tillage, and weed management as factors affecting weed communities and tested the hypothesis of an association between management practices and weeds from certain life cycle groups. Principal component analysis (PCA) of weed density data from a 4-yr field study conducted on a Kamouraska clay and a Saint-André gravelly sandy loam at La Pocatière QC, Canada, identified groups of weed species, while an analysis of variance (ANOVA) of PCA scores associated these groups with management factors. A multivariate analysis of variance (MANOVA) of regression coefficients describing time courses of density for each species confirmed treatment effects. Species segregated roughly according to life cycles. Interactions among weed management intensity, tillage, and crop rotation mostly explained species dominance in the various cropping systems. A first group of species, mostly annual dicots, largely dominated in minimum weed management treatments; their relative importance in each rotation varied with their level of susceptibility to postemergence herbicides. A second group included annuals and perennials, whose commonality seemed to be their tolerance to herbicides; these species also had a particular affinity for chisel and no-till treatments. A third group was formed by perennial species, each with a different response to tillage. The tenuous correspondence between commonly used classification schemes and management factors suggests that other aspects of weed biology (e.g., seed size, dispersal, production, germination requirements, and seedbank longevity) should be considered when trying to explain and predict the presence and dominance of certain weed species with regard to management practices.