The J. Derek Bewley Career Lectures presented at the triennial meetings of the International Society of Seed Science support early-career seed scientists by providing retrospective views, from those late in their careers, of lessons learned and future implications. Ambition, ability, inspiration, foresight, hard work and opportunity are obvious career requirements. The importance of mentoring and teamwork combined with the clear communication of results, understanding and ideas are emphasized. The role of illustration in research, and its dissemination, is outlined: illustration can support hypothesis development, testing and communication. Climate change may perturb the production of high-quality seed affecting conservation as well as agriculture, horticulture and forestry. An illustrative synthesis of the current understanding of temporal aspects of the effects of seed production environment on seed quality (assessed by subsequent seed storage longevity) is provided for wheat (Triticum aestivum L.) and rice (Oryza sativa L.). Seed science research can contribute to complex global challenges such as future food supplies from seed-propagated crops in our changing climate whilst conserving biological diversity (through seed ecology and technologies such as ex situ plant genetic resources conservation by long-term seed storage in genebanks), but only if that research can be – and then is – applied.

Plants that release molecules affecting other plants are a source of potential bioherbicides. Silver wattle (Acacia dealbata Link), considered invasive worldwide, was found to be phytotoxic to various other plant species. Combining the search for alternative bioherbicides while reducing the spread of this invader by preventing seed formation is a good potential strategy to solve both agricultural and environmental problems. This study aimed to identify nonvolatile compounds from A. dealbata flowers and explore their phytotoxicity on the germination process and seedling and plant growth of lettuce (Lactuca sativa L.), wheat (Triticum aestivum L.), and rigid ryegrass (Lolium rigidum Gaudin). We identified methyl cinnamate and methyl anisate as potential phytotoxins in the extracts, but we used pure commercial molecules to conduct bioassays. Methyl cinnamate showed higher phytotoxicity than methyl anisate and was selected for further bioassays. Methyl cinnamate reduced guaiacol peroxidase activity by 57% and 85% in L. rigidum and lettuce, respectively, and α-amylase by 6% in L. rigidum. This compound also inhibited early stem and radicle growth of dicotyledonous lettuce (60% and 89%, respectively) and monocotyledonous L. rigidum (76% and 87%, respectively), both species having small seeds. However, wheat with a larger seed size was not affected by the phytotoxin. The results obtained indicate a potential bioherbicidal effect for methyl cinnamate, and its application might be useful in wheat crops infested by L. rigidum. We suggest that collecting A. dealbata flowers would prevent Acacia seed formation and thus play a role in invasive pest management, as well as serving as a source of potential herbicides to other species.

The efficacy of herbicides applied broadcast by hand with a soil carrier or sprayed with water carrier were compared for Italian ryegrass control in winter wheat in central Oklahoma. Italian ryegrass was controlled 77 to 100% with BAY SMY 1500, chlorsulfuron, and CGA-131036 applied with both carriers. Metribuzin applied POST with 187 L ha–1 water was less phytotoxic to Italian ryegrass and wheat than with 200 kg ha–1 soil. All herbicides applied with 200 kg ha–1 silt loam soil as carrier at two locations controlled Italian ryegrass 96 to 100%. Increasing herbicide rate, soil carrier quantity, or broadcasting soil-carried herbicide in two directions rather than one did not significantly improve herbicide efficacy over that of conventional spraying.

Studies were conducted at the Main Agricultural Experiment Station in Fayetteville and the Vegetable Substation in Kibler, Arkansas, in 1992 and 1993 on the same plots to evaluate weed suppression by winter cover crops alone or in combination with reduced herbicide rates in no-till sweet corn and to evaluate cover crop effects on growth and yield of sweet corn. Plots seeded to rye plus hairy vetch, rye, or wheat had at least 50% fewer early season weeds than hairy vetch alone or no cover crop. None of the cover crops reduced population of yellow nutsedge. Without herbicides, hairy vetch did not suppress weeds 8 wk after cover crop desiccation. Half rates of atrazine and metolachlor (1.1 + 1.1 kg ai ha−1) reduced total weed density more effectively in no cover crop than in hairy vetch. Half rates of atrazine and metolachlor controlled redroot pigweed, Palmer amaranth, and goosegrass regardless of cover crop. Full rates of atrazine and metolachlor (2.2 + 2.2 kg ai ha−1) were needed to control large crabgrass in hairy vetch. Control of yellow nutsedge in hairy vetch was marginal even with full herbicide rates. Yellow nutsedge population increased and control with herbicides declined the second year, particularly with half rates of atrazine and metolachlor. All cover crops except hairy vetch alone reduced emergence, height, and yield of sweet corn. Sweet corn yields from half rates of atrazine and metolachlor equalled the full rates regardless of cover crops.

Scanning electron microscopy (SEM) was used to study alachlor microcapsule morphology and the effects of straw age and moisture on herbicide release. Microcapsule diameter in the formulation ranged from 2 to 15 μm. The polyurea encapsulating material was stable in water over time. Diffusion was suggested as the primary mode of alachlor release, with diffusion rate controlled by herbicide and salt concentration gradients between the microcapsule and the surrounding aqueous solution. Alachlor release was promoted by drying the microcapsules before addition to water. Microcapsule morphology was unchanged 48 h after application to dry straw, and microcapsules did not appear to adhere to the straw surface. Microcapsules applied to overwintered wet straw were shriveled at 48 h after treatment, indicating herbicide loss. Capsule walls were broken and appeared brittle after application to fresh wet straw. Organic constituents of the fresh straw cuticle may affect capsule wall integrity.

The allelochemicals 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA) and 6-methoxy-benzoxazolin-2-one (MBOA) in wheat are considered to have a role in plant defense against weeds. This study explored the effect of proximity to two weeds, wild oat and flixweed, on DIMBOA/MBOA production in wheat seedlings under hydroponic culture to identify whether the breeding of modern wheat varieties with higher concentrations of these compounds could ensure plant-mediated weed control. MBOA was detected and was noted to exert a significant response; its exudation by some wheat seedlings was significantly increased irrespective of whether the roots were in contact with or separate from those of the weeds. The weeds were a source of biotic stress to wheat when grown in proximity to it, and the stress resulted in production of higher levels of MBOA in wheat seedlings, although the concentration varied with the wheat cultivar. Therefore, the synthesis and exudation of DIMBOA/MBOA in wheat seedlings appears to be an active metabolic process influenced by the environment, particularly the presence of weeds.

Different herbicide-application strategies may serve as part of an integrated weed management (IWM) system. In 1987 and 1988, ten field trials were initiated in the south-central part of Sweden, with the objective of studying the long-term effects of herbicide-application strategies on the development of weed populations and productivity of spring-sown cereals. Each year until 1997, herbicides were applied at 25, 50, 75, or 100% of the full recommended dose. Treatments included herbicide exclusion every second year and herbicide application at 25 or 50% of a full dose during two out of three years, with a full dose applied in the third year. An untreated control was included. In 1998, weed densities in 25, 50, 75, and 100% of a full dose were reduced 43, 58, 64, and 67% compared with the control. At seven sites, the exclusion of herbicides every second year resulted in 43 to 178% higher weed densities than in 50% of a full dose, although the same amount of herbicide was applied when summarized over 2 yr. At four sites, herbicide application each year at 50, 75, or 100% of a full dose increased the density of difficult-to-control species by 24% compared with the untreated control. Averaged over sites, the untreated control contained 30% more weed species than herbicide application at 75 or 100% of a full dose. At three sites in 1996, the full dose resulted in 520 kg ha–1 (pooled over sites) higher barley yields than in the control. Neither in 1996 nor in 1997, was there any difference in crop yield between herbicide application at 25 and 100% of a full dose. This study demonstrates the potential of reducing the input of agrochemicals for weed control by using herbicides at reduced rates in competitive crops.

High levels of soil aluminium place serious constraints on wheat production on acidic soils, especially in the tropical areas of Africa and South America. Conventional plant breeding has improved the tolerance of the wheat crop, but available genetic variation is limited. The wild relatives of wheat provide a valuable gene pool for the introduction of further genetic variation. One wild species, Aegilops uniaristata Vis. (2n=2x=14,NN), is being utilized as a new source of tolerance. Of the addition lines of individual N genome chromosomes of A. uniaristata to wheat (Triticum aestivum L.) which have been established and characterized, chromosome 3N has been shown to confer tolerance to wheat. The three substitution lines in which 3N replaces the homoeologous wheat chromosomes, 3A, 3B or 3D, have also been produced. Growing plants to maturity in a low pH/high Al hydroponics system confirmed that chromosome 3N conferred tolerance to the substitution lines as well as to the addition line. By manipulating the genetic control of homoeologous chromosome pairing, chromosome 3N is being recombined with its wheat homoeologues in order to introduce a smaller alien segment which carries the gene(s) for tolerance but not the agronomically unacceptable brittle rachis gene also carried on chromosome 3N.