Until recently, phytopathogenic bacteria have not been considered potential biological weed control candidates because they lack the ability to penetrate intact plants. This deficiency can be overcome by providing entry wounds or using surfactants. Spray application of Pseudomonas syringae pv. tagetis (5 × 108cells/ml) in aqueous buffer with a surfactant produced severe disease in Canada thistle, common ragweed, Jerusalem artichoke, sunflower, and certain other members of the Compositae under field conditions. Spray application of the bacterium without surfactant was ineffective on all reported hosts. Xanthomonas campestris pv. poannua controlled annual bluegrass in bermudagrass golf greens when applied by spray during mowing. The bacterium entered through mowing injuries, causing lethal, systemic wilt. Application of the bacterium to annual bluegrass in the absence of fresh mowing injuries failed to produce symptoms. Under field conditions, this previously unknown pathovar's host range was limited to a single subspecies of annual bluegrass, but inundative application to freshly mowed turf resulted in infection of diverse annual bluegrass biotypes. In field trials, six monthly applications resulted in greater than 70% control. The preceding examples are among the first attempts to use foliar phytopathogenic bacteria for biological weed control. Efficacy of these bacterial bioherbicides and of future biocontrol strategies employing bacteria is dependent on facilitated host penetration.

Fumonisin B1 (FB1) sprayed on intact jimsonweed plants at 10 to 200 μg ml–1 caused chlorosis and necrosis on three- to four-leaf plants and reduced their height and biomass. Excised leaves of jimsonweed were necrotic on both surfaces after treatment with FB1 at 10 to 200 μg ml–1. The degree of damage increased with the concentration of FB1. The minimum amount of FB1 that damaged excised leaves was 0.05 μg. The symptoms of toxicity on sensitive plants varied with concentration of FB1. Symptoms observed included: chlorosis (creeping cucumber), necrosis (jimsonweed and common sunflower), black leaf lesions (sicklepod), curl of tissues (soybean), stunting, defoliation (hemp sesbania and northern jointvetch), and death (prickly sida, spurred anoda, northern jointvetch, and jimsonweed). Monocots (barley, bermudagrass, corn, johnsongrass, rice, sorghum, and wheat) were not visibly affected by FB1. This is the first evidence of the phytotoxic properties of fumonisin B1 against a wide variety of weeds and crop cultivars.

Horsenettle was described quantitatively in two grazed bermudagrass pastures for two years. Six times from April through October, plants were counted, phenologically documented, and tops were harvested for estimation of above-ground phytomass. Roots were sampled for carbohydrate, N fraction, and macronutrient analyses. Top growth, flowering, fruiting, and chemical composition were similar between sites within years, but differed between years. Starch and total non-structural carbohydrates in roots increased following reproductive periods both years. Root concentrations of protein and non-protein N increased and concentrations of P decreased in August and September in one year only. Analysis of the relationship between seasonal trends in carbohydrate fluctuation and pasture management practices suggests that systemic herbicide application in mid-summer may lead to more effective control than application in spring.