Field experiments were conducted in Louisiana over 2 yr to evaluate the influence of full-season interference from johnsongrass, common cocklebur, or hemp sesbania at densities of 2.5, 0.5, and 2.0 plants m–1 of row, respectively, and simulated insect defoliation of soybean on weed and soybean growth. Defoliation at R2 (full bloom) and R5 (beginning seed development) soybean growth stages was accomplished by removal of zero, one, or two leaflets per soybean trifoliate, which approximated 0, 33, and 66% defoliation, respectively. Height and dry weight of all weeds were not affected by soybean defoliation level or defoliation stage. Soybean height 3 wk after defoliation at R5 was not influenced by weed interference, soybean defoliation level, or defoliation stage in either year. Averaged across soybean defoliation levels and stages in 1994, johnsongrass, common cocklebur, and hemp sesbania reduced soybean yields 30, 15, and 14%, respectively. In 1995, johnsongrass reduced soybean yield 35%. As soybean defoliation level increased, a linear decrease in soybean yield was observed. Averaged across weeds and soybean defoliation stages, 33 and 66% defoliation reduced soybean yield 6 and 20% in 1994 and 12 and 33% in 1995, respectively. Defoliation at R5 resulted in 10% lower yield than defoliation at R2 in one of two years. Yield reduction due to combinations of weeds and soybean defoliation was additive.

Glycine max fields with Sesbania exaltata and Senna obtusifolia were selected to evaluate weed effects on insecticide spray droplet deposition within the crop canopy and soybean looper (Pseudoplusia includens) mortality. Weedy and weed-free treatments with and without thiodicarb insecticide application were included. Soybean looper populations in plots with S. exaltata and S. obtusiolia were approximately half those found in weed-free plots. Thiodicarb reduced soybean looper larval survival in the absence of weeds or when weeds were present in three of four experiments. Dye-sensitive cards placed in the top, middle, and bottom thirds of the G. max canopy showed droplet coverage to be highest on cards placed in the top of the canopy. Weeds reduced insecticide coverage in the top of the G. max canopy 26 to 43%. Thiodicarb deposition within the middle and bottom levels of the canopy was not reduced by weeds. Leaflets from the top, middle, and bottom thirds of the crop canopy were collected immediately after insecticide application to bioassay for insecticide deposition. For both years, mortality of soybean looper larvae on leaflets collected from the middle or top of weedy and weed-free G. max treated with thiodicarb was equivalent. Assuming that an economic return can be expected, soybean looper management may not need to be altered when moderate infestations of S. exaltata and S. obtusifolia are present in G. max in late season.

With the shift to earlier maturing soybean cultivars, harvest interference data are needed at low weed densities that will not reduce yield, but may affect soybean quality or harvesting efficiency. Field experiments were conducted in 1995 and 1996 to determine the density of five weeds necessary to warrant desiccation treatments. There were no consistent differences in losses of harvestable soybean due to weed density. Common cocklebur increased foreign material and soybean moisture at a greater rate than did hemp sesbania, ivyleaf morningglory, or redroot pigweed, with sicklepod intermediate among these species. Soybean test weight was reduced by 17, 13, and 59 g/L for each plant/meter of row with redroot pigweed, sicklepod, and common cocklebur, respectively, whereas hemp sesbania and ivyleaf morningglory did not affect test weight. However, all species evaluated increased damaged soybean seeds by 8.2 to 11.1% for each plant/meter of row. Combine speed was not affected substantially by the weed densities evaluated.

Greenhouse studies were conducted to determine host status of weed species for Rhizoctonia solani AG-1, which causes Rhizoctonia foliar blight of soybean. Weed species were barnyardgrass, broadleaf signalgrass, common cocklebur, entireleaf morningglory, hemp sesbania, itchgrass, johnsongrass, large crabgrass, northern jointvetch, prickly sida, purple nutsedge, redweed, sicklepod, and smooth pigweed. Seedling weeds were inoculated with suspensions containing intraspecific group IA and IB isolates of the fungus. In the first study, sclerotia of IA were recovered from tissue of all weeds except smooth pigweed, and mycelia of IA were recovered from all except smooth pigweed and redweed. In that study, neither microsclerotia nor mycelia of IB were recovered from sicklepod, barnyardgrass, or large crabgrass, and only microsclerotia were recovered from itchgrass and purple nutsedge. In the second study, sclerotia of IA, microsclerotia of IB, and mycelia of each isolate were recovered from all weed species. In other studies, R. solani spread from at least six of seven weed species to a noninfected soybean plant growing in close proximity. These studies emphasize the importance of weed control, not only for reducing plant competition and increasing yield, but also for the potential impact on development of RFB.

Full-season interference effects of hemp sesbania [Sesbania exaltata (Raf.) Cory. # SEBEX] on cotton (Gossypium hirsutum L. 'Stoneville 213′) were investigated on a fine sandy loam soil for 3 yr at Stoneville, MS. Experimentally induced hemp sesbania populations of ≥ 3223 plants/ha significantly reduced cotton yields. Interference of hemp sesbania at 3223, 6456, 16 114, and 32 228 plants/ha, equivalent to 1, 2, 5, and 10 plants/3.3 m, reduced seed cotton yields by 19, 25, 45, and 53%, respectively. Cotton boll weights were reduced by 9% when hemp sesbania infestations were ≥ 16 114 plants/ha. Cotton plant density, seedling vigor, and initial cotton white blooms/ha at ≤75 days after planting (DAP) did not differ with varying densities of hemp sesbania. Cotton white blooms/ha were reduced by 32 228 hemp sesbania plants/ha by 77 DAP and by all weed densities by 98 DAP. Hemp sesbania height was equal to or greater than cotton height by 55 to 65 DAP. Light penetration at 1 m above the top of the cotton canopy was 36% less than in weed-free plots when hemp sesbania densities were ≤6446 plants/ha. Likewise, light penetration was reduced at the cotton canopy top and at midcanopy but was not less at the soil surface unless hemp sesbania densities were ≤ 32 223 plants/ha.

The weed control spectrum of clomazone, the influence of clomazone on the performance of other herbicides, and the performance of tank mixtures containing clomazone were evaluated from 1985 through 1987. Clomazone applied preemergence at 280 g ai/ha controlled 90 to 100% of barnyardgrass, giant foxtail, goosegrass, large crabgrass, seedling johnsongrass, prickly sida, and velvetleaf. Clomazone at reduced rates was more effective applied preemergence than preplant-incorporated for 10 of 23 weed species. Clomazone enhanced imazaquin activity on entireleaf morningglory and sicklepod in 1986. A tank mixture of clomazone, imazaquin, and metribuzin at half the labeled rates reduced soybean injury, increased soybean yield, and controlled weeds as well as the mixture at labeled rates.

In greenhouse experiments, conidia of Colletotrichum truncatum applied in an invert emulsion formulation controlled hemp sesbania 100% in the absence of a dew treatment. In field experiments, hemp sesbania control averaged 95 and 97% in 1989 and 1990, respectively, when this formulation was applied to hemp sesbania seedlings using tractor-mounted, air-assist nozzles. This level of weed control was comparable to that achieved from the herbicide acifluorfen. These results indicate that C. truncatum has excellent potential as a mycoherbicide for controlling hemp sesbania and that this potential can be augmented by formulating the pathogen as an invert emulsion.

Hemp sesbania interference in cotton was investigated in the greenhouse and in a 2-yr field experiment at Stoneville, MS. In greenhouse experiments, cotton and hemp sesbania heights and plant dry weights (PDW) were not different in ratios of cotton to hemp sesbania of 4:0, 2:2, 1:3, and 0:4 at 3 and 5 wk after emergence (WAE). Hemp sesbania PDW were less for ratios of cotton to hemp sesbania of 3:1 when compared to hemp sesbania PDW of other ratios. Early season cotton seedling vigor and growth (0 to 28 DAP) were not affected by 32 000 hemp sesbania plants ha-1 (3 plants m of row-1). Hemp sesbania plants were hand removed 28, 42, 56, 70, and 84 d after planting (DAP). White cotton blooms and yields were reduced when hemp sesbania plants were not removed by 70 DAP. Seed cotton yields were 2590, 2570, 2460, 2030, 1610, and 1070 kg ha-1 for hemp sesbania removed at 28, 42, 46, 70 and 84 DAP or not removed, respectively. The critical period of weed control or removal of hemp sesbania in cotton is ≤62 DAP.

Metribuzin and the ethyl ester of chlorimuron were evaluated alone and in combination for preemergence broadleaf weed control in soybeans. Neither herbicide alone controlled all broadleaf weeds tested, but combinations showed both complementary and additive action. Two field studies quantified these interactions on broadleaf weeds and showed that low rates of either herbicide alone controlled Pennsylvania smartweed and redroot pigweed. Metribuzin was more effective than chlorimuron in controlling prickly sida and hemp sesbania, while chlorimuron was more effective on common cocklebur, sicklepod, and ivyleaf and pitted morningglories. Additive action was most important on velvetleaf, sicklepod, annual morningglories, and hemp sesbania. Because the components were both additive and complementary, a range of mixture rates and ratios were more effective for weed control than either herbicide alone.

Experiments were conducted at three locations in Louisiana from 1992 to 1994 to evaluate broadleaf weed control with sulfentrazone. Sulfentrazone at 0.42 kg ai/ha applied PPI or PRE provided at least 93% control of entireleaf morningglory in all years at all locations, which was greater than control with metribuzin PRE. Prickly sida control with sulfentrazone ranged from 83 to 94%, which was equal to or greater than control with metribuzin. Hemp sesbania and sicklepod control with sulfentrazone was unacceptable (≤75%) regardless of application method and generally was lower than control with metribuzin. Greater than 90% control of smellmelon and hophornbeam copperleaf was observed with all treatments. Minor but transient soybean injury was noted at one location in one year. Soybean yields following sulfentrazone PRE at St. Joseph were greater than yields with metribuzin as a result of the general increase in broadleaf weed control.

Hemp sesbania control by chlorimuron applied with crop oil concentrate at 1.0% v/v, BCH 815 at 1.0% v/v, methylated seed oil at 1.0% v/v, a blend of methylated seed oil and organosilicone surfactant at 0.5% v/v, organosilicone-based surfactant at 0.125% v/v, and nonionic surfactant at 0.25% v/v was evaluated in field studies in 1994 and 1995. Control by chlorimuron at 4.5 g ae/ha was greater when applied with BCH 815, organosilicone-based surfactant, and nonionic surfactant than with crop oil concentrate, methylated seed oil, and a blend of methylated seed oil and organosilicone surfactant. When chlorimuron was applied at 4.5 g/ha with BCH 815 or nonionic surfactant, hemp sesbania control was similar to that by chlorimuron at 9 g/ha applied with methylated seed oil, the blend of methylated seed oil and organosilicone surfactant, or organosilicone-based surfactant.

A 3-yr study was conducted to compare the performance of several herbicides applied alone and in mixtures under three flooding conditions in dry-seeded rice (Oryza sativa L. ‘Labelle’). When the soil remained moist during the 2-week unflooded periods (1979 and 1981), weed emergence was slowed and no advantage with respect to enhanced weed control and increased rice yields could be demonstrated over that of the standard sequential propanil (3′,4′-dichloropropionanilide) application. However, in 1980 when drought stress may have reduced initial postemergence activity and weeds emerged during the 14-day unflooded periods, differences in weed control between herbicides were obtained. Results of this study also indicate that yield losses from weed competition resulted primarily from early season competition, and that the principal advantage of the residual herbicides in dry-seeded rice may be to eliminate the need for retreatment with propanil when flooding is delayed or fields are drained.

Greenhouse studies were conducted to investigate the effects of adjuvant and rainfall on bentazon spray retention, efficacy, and foliar washoff in hemp sesbania, sicklepod, smooth pigweed, and velvetleaf. Bentazon was applied at 0.28 to 2.24 kg ai/ha with Agri-Dex, a crop oil concentrate (COC) or Kinetic, an organiosilicone-nonionic surfactant blend (OSB) when weeds were at the three- to five-leaf stage. Plants were subjected to 2.5 cm simulated rainfall for 20 min at 1 and 24 h after application of bentazon. Shoot fresh weight reduction assessed 2 wk after treatment was similar with either adjuvant on velvetleaf and smooth pigweed. OSB enhanced bentazon efficacy in hemp sesbania and sicklepod as compared to COC. Rainfall at 1 h after application generally reduced bentazon activity in all weeds. OSB maintained bentazon activity in hemp sesbania when subjected to rainfall at 1 h after application as compared to COC. Overall, bentazon spray retention on plants was 9 to 550% higher with OSB as compared to COC among the species at 1 h after application. Amount of bentazon residue washed off from the foliage by rainfall within a weed species was relatively similar for both adjuvants except in smooth pigweed and ranged from 39 to 98% among the four weed species at 1 h after application. OSB exhibited specificity for certain weed species and the potential to minimize bentazon spray reaching the soil by increasing deposition.

Field experiments were conducted from 1993 to 1995 to compare weed control by the isopropylamine salt of glyphosate at 0.21, 0.42, 0.63, and 0.84 kg ae/ha applied at three stages of weed growth. Weed control by glyphosate applied at these rates alone or with ammonium sulfate at 2.8 kg/ha was also evaluated. In other experiments, potential interactions between glyphosate and acifluorfen, chlorimuron, and 2,4-DB were evaluated. Velvetleaf, prickly sida, sicklepod, pitted morningglory, entireleaf morningglory, palmleaf morningglory, and hemp sesbania were controlled more easily when weeds had one to three leaves compared with control when weeds had four or more leaves. Glyphosate controlled redroot pigweed, velvetleaf, prickly sida, sicklepod, and barnyardgrass more effectively than pitted morningglory, entireleaf morningglory, palmleaf morningglory, or hemp sesbania. Increasing the rate of glyphosate increased control, especially when glyphosate was applied to larger weeds. Greater variation in control was noted for pitted morningglory, palmleaf morningglory, prickly sida, and velvetleaf than for redroot pigweed, sicklepod, entireleaf morningglory, or hemp sesbania. Ammonium sulfate increased prickly sida and entireleaf morningglory control but did not influence sicklepod, hemp sesbania, or barnyardgrass control. Acifluorfen applied 3 d before glyphosate or in a mixture with glyphosate reduced barnyardgrass control compared with glyphosate applied alone. Chlorimuron did not reduce efficacy. Mixtures of glyphosate and 2,4-DB controlled sicklepod, entireleaf morningglory, and barnyardgrass similar to glyphosate alone.

Field experiments were conducted in 1986, 1987, and 1988 to evaluate imazethapyr rate and time of application on postemergence control of 24 weed species. Contour graphs were developed that predicted imazethapyr rates required for various levels of weed control based upon weed leaf number at application. Rates below the labeled rate (70 g ha−1) provided 90% or greater control of common cocklebur, smallflower morningglory, and smooth pigweed if applied to 3 true-leaf or smaller weeds and of barnyardgrass, seedling johnsongrass, and Palmer amaranth if applied while weeds were in the cotyledon or 1 true-leaf stage. A rate of 70 g ha−1 provided 90% control of large crabgrass in the 1 true-leaf stage. Entireleaf morningglory, red rice, pitted morningglory, and velvetleaf are not susceptible enough to imazethapyr for 90% or greater control to be obtained with rates lower than 70 g ha−1 at the 1 true-leaf growth stage. These data demonstrate how control data can be used for developing effective reduced-rate herbicide recommendations based on weed leaf number.

A tandem mass spectrometric procedure was developed to detect sesbanimide A and its isomers in plant materials. Analysis of seed extracts from 10 Sesbania species using this procedure readily detected sesbanimides in Drummond rattlebush, rattlebush, and bagpod sesbania. The toxic sesbanimides were not detected in hemp sesbania or in other species with no known history of animal toxicity.

Sicklepod (Cassia obtusifolia L. ♯6 CASOB), hemp sesbania [Sesbania exaltata (Raf.) Cory ♯ SEBEX], and showy crotalaria (Crotalaria spectabilis Roth. ♯ CVTSP) were grown in controlled-environment greenhouses with day/night temperatures of 23/17, 26/20, 29/23, and 32/26 C. Plant height, leaf area, and total dry weight at 53 days after planting increased significantly with temperatures between 23/17 and 29/23 C in sicklepod and showy crotalaria, and between 23/17 and 32/26 C in hemp sesbania. In all species, leaves were produced more rapidly as temperature increased. Axillary branch leaf production was greatest at 29/23 C in sicklepod, and at 29/23 and 26/20 C in showy crotalaria; hemp sesbania showed little axillary branch development. Total dry-matter production in all species was closely correlated with leaf area duration, but not with net assimilation rate. Differences in total main stem leaf area in all species were primarily due to differences in leaf number rather than to differences in leaf size at maturity.

Field studies were conducted from 1988 to 1990 on a Sharkey clay to evaluate residual weed control in rice with quinclorac applied PPI, PRE to dry soil, and PRE to moist soil. Quinclorac applied at 0.4 or 0.6 kg ai ha−1 PPI or PRE to dry or moist soil controlled more than 80% of barnyardgrass, pitted morningglory, and hemp sesbania without rice injury. Quinclorac applied at 0.3 kg ha−1 controlled these three weed species substantially but inconsistently. No rice injury was observed from any quinclorac treatment. Except for one of three years when irrigation was delayed for 7 d after PRE application to dry soil, application timing did not consistently affect weed control or rice yield.

In greenhouse experiments, unrefined corn oil was tested as an adjuvant with the mycoherbicidal fungus, Colletotrichum truncatum. A1:1 (V/V) fungus/corn oil tank mixture extended by at least 70 h the period of time in which the fungus remains infective between inoculation and the onset of dew. This formulation also reduced the dew period requirements for optimal weed pathogenesis and mortality from 12 h to 2 h, and reduced the required spray volume by 100-fold, from 500 L/ha to 5 L/ha. These results suggest that formulating C. truncatum in unrefined corn oil greatly improves the bioherbicidal potential of this pathogen.

Soybean yield loss from weed interference depends upon weed density and competitiveness of crop and weed species in response to environment. Soil water availability and nitrogen fertility were evaluated for their effect on competitiveness of individual species in field experiments. Early-season temperatures in 1995, which were cool compared to 1994, slowed hemp sesbania growth without affecting soybean growth. This resulted in negligible competition with soybean by hemp sesbania at densities of 3 or 6 plants m−2. In 1994, hemp sesbania grew above the soybean canopy, decreasing soybean light interception 29 to 68%, and reducing soybean yield 30 to 48%. Fertilizer nitrogen increased soybean competitiveness, as indicated by biomass production, only in irrigated plots with hemp sesbania at 3 m−2, but did not affect soybean yield. Apparently, competition for light is a primary cause of soybean yield loss from hemp sesbania infestations. In growth chamber studies, simulating temperatures from the field, hemp sesbania growth was stimulated more by warm temperatures than was soybean. Hemp sesbania and soybean dry weights increased 4.4- and 2.7-fold, respectively, at 30/20 C day/night temperatures compared to 25/15 C.