The influence of ultraviolet-B (UV-B) radiation on seedling growth and leaf surface characteristics of important rangeland weeds Cynoglossum officinale L. (houndstongue), Centaurea diffusa Lam. (diffuse knapweed), and Tragopogon pratensis L. (meadow salsify) was investigated in a greenhouse by exposing seedlings to 0, 7, or 11 kJ m−2 d−1 of biologically effective UV-B radiation. UV-B radiation reduced leaf, stem, and root fresh weights, leaf area, and leaf: shoot ratio and increased shoot dry matter content, specific leaf weight, and leaf greenness of C. officinale seedlings. Leaf, stem, and root fresh weight, and leaf area of C. diffusa seedlings decreased, whereas shoot dry matter content, specific leaf weight, leaf: shoot ratio, and leaf greenness were unaffected. T. pratensis seedlings exposed to UV-B radiation had diminished leaf greenness, but no change was observed in leaf or stem fresh weight, leaf area, or leaf: shoot ratio. Uniseriate trichome abundance in C. officinale seedlings increased and trichome orientation changed in response to UV-B exposure. UV-B treatments decreased uniseriate trichome abundance in C. diffusa; glandular trichome abundance and the ratio of glandular: uniseriate trichomes were not affected. T. pratensis seedlings showed no change in the amount of epicuticular wax on the adaxial leaf surface in response to UV-B irradiation. Shoot dry weight was not influenced by removal of epicuticular wax prior to UV-B exposure. Results suggest that epicuticular wax is not an important factor in acclimation of T. pratensis seedlings to UV-B radiation. Susceptibility to UV-B–induced damage was greatest for C. officinale seedlings and least for T. pratensis seedlings. Modification of plant morphology or reduction in growth induced by enhanced UV-B radiation may influence competitive relationships between rangeland weeds and their associated forage species.

The reproductive characteristics of natural populations of meadow salsify were monitored between May 1990 and October 1991. Plants in even-aged populations did not produce seeds prior to the second winter and plants in uneven-aged populations died after seed production suggesting that meadow salsify at this site is a monocarpic perennial and not a true biennial. Delayed seed production may enhance abundance of this species by increasing the size of its bud bank. Plants of uneven-aged populations flowered over a range of root crown diameters; the percentage of plants bearing flowers increased with increasing root crown diameters. The minimum root crown diameter at which plants flowered in 1990 and 1991 was 0.2 and 0.6 cm respectively demonstrating that factor(s) other than plant size regulate flowering in this species. Seed production ranged between 100 to 850 seeds per plant. Total number of flower heads per plant and florets per plant were positively correlated with each other and with the root crown diameter. Root crown diameter is, therefore, a good indicator of potential fecundity in meadow salsify. Greater seed production by larger plants may compensate, at least in part, for the high juvenile mortality and longer generation time in this species. The results suggest that prolific seed production and long vegetative survival are important strategies in the maintenance of meadow salsify populations.

To understand the role of the seed coat in regulation of houndstongue seed dormancy, the effects of manipulation of seed coat integrity on seed germination and O2 uptake were studied. The results suggest that the seed coat of this weed regulates dormancy in part by interfering with the diffusion of O2 to the embryo. Scanning electron microscopy showed a network of ridges on the seed coat surface that were partially dissolved following 1.5 min of sulphuric acid scarification. Mechanical scarification removed fragments of the seed coat surface. Both scarification treatments stimulated seed germination. Supply of an elevated level of O2 also stimulated seed germination. O2 uptake by seeds imbibed in O2-saturated water was 150% higher than that for seeds imbibed in air-saturated water. Although all treatments that stimulated seed germination also stimulated O2 uptake, there was a lack of a consistent, quantitative relationship between increases in O2 uptake and seed germination in various experiments. This suggests that limitation of O2 availability to the embryo is not the only factor involved in regulation of houndstongue seed dormancy by the seed coat. Mechanical restriction of embryo expansion by the seed coat may also be important. Methanol-insoluble phenolics constituted < 1% of the total phenolic pool in the embryo. Their potential oxidation could not account for more than a small fraction of the previously reported massive stimulation of O2 uptake by the embryo upon decoating. The present O2 uptake and seed germination studies indicate that not all of the large increase in O2 uptake following decoating is essential for houndstongue seed germination.

Seasonal changes in germination behaviour of meadow salsify seeds buried at different depths, and survivorship of seed and plant populations were investigated. Freshly matured seeds were mixed with sterilized soil, placed into nylon mesh bags, and buried at three soil depths in a meadow salsify-infested rangeland. Two germination peaks were observed: one in the fall, 2 to 3 mo after burial, and a second the following spring. Burial depth affected seed dormancy. The number of seeds with enforced dormancy, and innate or induced dormancy, increased with burial depth in the 1989 cohort, and the number with enforced dormancy increased in the 1990 cohort. Burial depth also affected seed survivorship. The survivorship curves for 1989 and 1990 seed cohorts were not different as indicated by the Logrank test. The seed population was nearly depleted after 9 to 10 mo of burial; less than 3 % of the buried seeds remained viable after 13 mo. About 50% of the plants monitored in a natural meadow salsify population in 1990 died before winter, and an additional 35% died during winter. The mortality of the remaining plants during the second growing season was very low. Only 12% of the 1990 cohort remained in October 1991. Mortality of meadow salsify plants was density-independent.

Weed control in cole crops and onion by postemergence spraying with liquid ammonium nitrate was studied to determine its feasibility under Fraser Valley, British Columbia conditions. Ammonium nitrate solutions (7.5, 10, 15 and 20% N) were applied at 800 L ha−1 on warm, sunny days. Shepherd's-purse, low cudweed, redroot pigweed and ladysthumb were susceptible to this treatment; common lambsquarters, common purslane and annual bluegrass were tolerant. In order to determine the effect of weed density on weed control, several shepherd's-purse densities were established in broccoli and sprayed with ammonium nitrate solution (20% N; 800 L ha−1). Two days after treatment, weed control was 87.2% for an initial density of 500 shepherd's-purse plants m−2 (1987) and 76.1% for an initial density of 988 plants m−2 (1988). The seedlings that survived the treatment were sufficiently set back that they did not cause any adverse effect on crop yield. In a separate study, cabbage and onion were found to be tolerant to the ammonium nitrate treatment. Initially, cauliflower, broccoli and Brussels sprouts growth was slightly inhibited by the ammonium nitrate treatment but the plants recovered and crop yield was not affected.

To understand persistence strategies of meadow and western salsify, ecophysiological characteristics of their seed germination were studied. Anaerobiosis (immersion in deoxygenated water) induced secondary dormancy in seeds of both species. Dormancy could be induced in 86% of meadow salsify seeds and in 65% of western salsify seeds by a 1-d anaerobiosis treatment. The induced dormancy was gradually released during storage of air-dried secondary dormant meadow salsify seeds, and the rate of this release was influenced by storage temperature; 30 C was more effective than 10 or 20 C in releasing secondary dormancy. These results suggest that the two species may rely on induced dormancy as an option in their persistence strategy. The optimum temperature for germination of nondormant seeds of both species was 15 C. Maximum germination percentages for both species were established within 4 to 6 d of incubation at 15 C and within 14 to 28 d of incubation at 25 C. Nondormant seeds did not germinate below 10 or above 30 C. Stratification (at 5 C for 2 to 10 wk) stimulated germination of secondary dormant seeds of meadow salsify. This stratification requirement can be important in preventing germination of dormant salsify seeds in the fall, thereby avoiding high seedling mortality in the winter. Light (red and far-red) had no effect on germination of seeds in secondary dormancy. In a separate study, seeds of both species were planted in pots at depths of 2 to 14 cm and seedling emergence was observed. Maximum emergence occurred when seeds were buried 2 cm deep. Seeds planted 8 cm or deeper germinated but did not emerge.

Influence of aqueous leaf extracts, leaf residue, and leached-leaf residue of houndstongue, a noxious rangeland weed, on seedling emergence of forage grasses was studied. Ultraviolet-B (UV-B) effects during houndstongue growth on subsequent germination and growth-inhibitory activity of leaf extracts were investigated. Addition of glasshouse-grown houndstongue leaf extract to mineral soil decreased emergence of crested wheatgrass by 13% and prairie junegrass by 20% at 14 d after sowing. Idaho fescue emergence was unaffected. Incorporation of houndstongue leaf- and leached-leaf residue into soil (0.4 g residue : 20 g soil) delayed emergence of forage grasses. At 14 d after sowing, houndstongue leaf residue spread on the soil surface (0.2 g residue : 20 g soil) tended to inhibit seedling emergence more than leaf residues incorporated into soil. In separate experiments, houndstongue plants were grown at 0, 4, 7, and 11 kJ/m2/d biologically effective UV-B radiation for 6 wk, and leaf extracts (0.5, 1, 2, and 4% wt/v) were prepared. Exposure of houndstongue to increasing UV-B dose during plant growth generally increased the inhibitory activity of their leaf extract on prairie junegrass germination. Crested wheatgrass and Idaho fescue seedlings incubated in extracts of houndstongue leaves exposed to UV-B, compared with leaves grown in a UV-B–free environment, had decreased root lengths. Leaf extracts of plants exposed to elevated UV-B levels had higher absorbance at 300 nm, indicating greater concentration of UV-B–absorbing compounds. This study suggests houndstongue leaf extracts and residues inhibit seed germination and seedling emergence and that UV-B may enhance their allelopathic influence on some forage grasses. Field studies are needed to confirm the allelopathic influence of houndstongue under rangeland conditions.

Herbicidal activities of clove oil and its primary constituent eugenol on broccoli, common lambsquarters, and redroot pigweed and the role of crystalline leaf epicuticular wax (LEW) in susceptibility and retention of these essential oils were studied. Clove oil (2.5%) and eugenol (1.5%) were applied to leaves of greenhouse-grown broccoli, common lambsquarters, and redroot pigweed seedlings and effects on seedling growth and leaf cell membrane integrity were studied. Compared with eugenol, clove oil caused greater inhibition of seedling growth in all species. Both eugenol and clove oil caused greater loss of membrane integrity and inhibition of seedling growth in redroot pigweed, which has no crystalline LEW, compared with common lambsquarters, which has a thick layer of crystalline LEW. In broccoli seedlings with LEW, clove oil caused greater inhibition of growth than eugenol. Both clove oil and eugenol caused greater electrolyte leakage from broccoli leaves without LEW than in the leaves with LEW. Removal of LEW increased electrolyte leakage, an indicator of cell membrane damage, by 97% in eugenol-treated and 26% in clove oil–treated broccoli leaves. Susceptibility of broccoli seedlings and possibly some weed species may, therefore, be affected by factors (e.g., genetic, environmental) that influence the amount of LEW. Although the presence of LEW greatly reduced the retention of the essential oil solutions, there was no significant difference between the retention of clove oil and eugenol solutions, indicating that differences in their phytotoxicity to broccoli leaves was not due to differential foliar retention.

Herbicidal activity of clove oil and its main constituents eugenol, β-caryophyllene, and α-humulene was studied by measuring their effects on cell membrane integrity in broccoli and common lambsquarters plants at the three- and nine-leaf stage, respectively. Roles of essential oil constituents in the overall phytotoxicity of clove oil, dose-response (10 to 160 mM) relationships of their phytotoxicity, and the effect of light intensity on phytotoxicity of clove oil and eugenol were studied. Most of the phytotoxicity of clove oil (2.5% solution) was due to eugenol, its largest constituent. β-caryophyllene and α-humulene played little or no role. Dose-response relationships showed that at equimolar concentration, eugenol was the most phytotoxic essential oil constituent of the clove oil. On a per unit biomass basis, membrane damage in response to clove oil and eugenol sprays decreased with increasing light intensity. This suggests that efficacy of essential oil in causing plant damage could be affected by light intensity experienced by plants prior to the oil spray.

Ultraviolet-B (UVB, 280 to 320 nm) radiation levels reaching the earth's surface are increasing because of depletion of the stratospheric ozone layer. Adverse biological effects of this harmful radiation are a serious concern. The effects of UVB radiation on spotted chickweed, dandelion, downy brome, green foxtail, redstem filaree, and common catsear seed germination, shoot and radicle elongation, and seedling growth and development in a UVB-free environment after exposure to UVB were investigated in a greenhouse study. UVB radiation (4, 7, or 11 kJ m−2 d−1) did not influence seed germination of any species except downy brome. Postgermination UVB exposure (8 h d−1, for 10 d), however, inhibited radicle elongation in all species, except in spotted catsear. Shoot elongation was also inhibited in some species but to a lesser extent than radicle elongation. A significant inhibition by UVB treatment (11 kJ m−2 d−1) of root and shoot biomass, leaf area, and leaf number was observed in some species after transfer of UVB-treated seedlings to a UVB-free environment for 3 wk. The inhibition of postgermination shoot and radicle elongation by UVB radiation, the continuation of growth inhibition after transfer of the treated seedlings to a UVB-free environment, and the differential responses of weedy species could have significant implications for their ability to compete with each other and with associated crops in a UVB-enriched environment that is likely as the stratospheric ozone layer gets depleted.

Hound’s-tongue is an invasive, biennial weed that thrives in dry rangelands of British Columbia. Rosette formation in the first year of growth and a deep root system offer this weed a competitive advantage against associated grasses under dry conditions. To study effects of water stress on seedling growth and mycorrhizal colonization in hound’s-tongue, seedlings of this weed were grown in pots in a greenhouse and subjected to four (100, 80, 60, and 40% of field capacity) soil moisture treatments. Effects of soil moisture stress (SMS) on several growth parameters as well as mycorrhizal colonization of roots were studied. The total biomass, shoot and root fresh and dry weights, leaf number, petiole length, leaf area, and specific leaf weight (leaf dry weight per unit leaf area) decreased with increasing SMS; shoot and root water content was not affected. Because of a greater effect of SMS on root compared with the shoot biomass, shoot:root ratio increased as the moisture stress increased. Water stress decreased mycorrhizal colonization and arbuscule and vesicle abundance. A reduction in total biomass, leaf number and leaf area per plant, petiole length, and mycorrhizal colonization may reduce the competitive advantage of hound’s-tongue over its neighbors under drought conditions. The effect on plant size may also influence herbivory, by biocontrol agents and other herbivores, and fecundity of this weed.