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Current guidelines for phytotoxicity testing rely heavily on short-term testing of primarily crop species to predict the sensitivity of non-target, wild plants to herbicides. However, little is known on how plants recover following initial growth inhibitions in standard 14-28 day greenhouse tests conducted for pesticide assessment and registration. The objectives of this study were to assess the ability of plant species to recover (biomass and reproduction) when tested at the juvenile stage (routine regulatory testing), comparing crop and wild species and using the herbicide glufosinate ammonium. Ten crops and 10 wild species were tested with a one-time exposure to glufosinate ammonium in a greenhouse. Half the plants of each species (9 doses × 6 replicates) were harvested 3 weeks after being sprayed (short-term). The remaining plants were harvested several weeks later, coinciding with seed set or natural senescence (long-term). Total aboveground biomass and several endpoints related to crop production and plant reproduction were measured. Calculated IC50 values (dosage that results in a 50% decrease in the biomass of a plant as compared to the untreated controls) based solely on aboveground biomass, for species harvested in the long-term were generally higher than those obtained in the short-term (with two exceptions), indicating recovery over time. Crop species did not differ from wild species in terms of sensitivity. However, in seven out of 12 cases where reproduction was measurable, reproductive endpoints were more sensitive than either short or long-term biomass endpoints, indicating the importance of examining these parameters in phytotoxicity testing. Glufosinate ammonium was found to be phytotoxic at low doses (2.64-7.74% g ai/ha of the label rate).

We report on the free diffusion of single molecule near an interface studied using fluorescence correlation spectroscopy. In particular, we show that the chemical nature of the substrate may modify the free diffusion of a widely used molecule (rhodamine 6G), thus inducing unexpected effects in fluorescence correlation spectroscopy measurements. Our results show a strong influence, up to a few micrometer from the interface, of the surface polarity. This effect is assessed through the relative weight of the two dimensions diffusion process observed close to the surface. Our results are discussed in terms of competition between surface-solvent, solvent-molecule and molecule-surface specific interactions.