Downy brome seed production was measured in the field following the establishment of different moisture levels using a line source sprinkler irrigation system. Results indicated that seed production was strongly affected by different moisture levels, with a curvilinear decrease in seed number from higher to lower moisture. In a hydroponic study with water deficits induced by PEG-8000, no seeds were produced when plants were severely stressed (-1.1 MPa) for a 7-day period during culm elongation or anthesis. Number of seeds/panicle was reduced under severe water stress during seed fill, under moderate stress (-0.5 MPa) during anthesis or seed fill, and under mild stress (-0.1 MPa) during anthesis. Water stress also reduced apparent photosynthesis and increased diffusive resistance of flag leaves, particularly under severe stress. In general, water deficits did not affect seed weights or germination percentages in either study.

Common cocklebur, jimsonweed, and velvetleaf were grown with soybeans in the field to determine how soybean interference affects weed canopy architecture. Common cocklebur had more leaves within the soybean canopy than jimsonweed or velvetleaf. At the end of the season, common cocklebur leaf area was distributed evenly below and above the top of the soybean canopy, while nearly all the jimsonweed and velvetleaf leaf area was above the soybean canopy. Common cocklebur exhibited more shade tolerance than jimsonweed or velvetleaf by also maintaining leaves in the shade within the soybean canopy. Differences among these weeds in leaf distribution within the soybean canopy were not related to differences in abscission of the lower leaves but to a differential response of lower axillary buds to soybean shading. Growth from lower axillary buds in jimsonweed and velvetleaf was strongly inhibited by soybean interference, but interference had little effect on lower axillary bud growth in common cocklebur. Axillary bud growth in the lower canopies of both common cocklebur and soybeans, and their similarity in height, caused these plants to compete for the same aboveground niche. However, common cocklebur had more extensive axillary growth along the lower stem than soybeans, which may allow it to compete for resources in this niche more aggressively than soybeans. Velvetleaf and jimsonweed did not share the same aboveground niche with soybeans due to the placement of their leaves above rather than within the soybean canopy. The lower branching characteristics and apparent shade tolerance of common cocklebur may be important factors in the superior competitive ability with soybeans compared to jimsonweed and velvetleaf.

Bermudagrass plugs were transplanted from the greenhouse to the field at monthly intervals from March through October at Shafter, CA. Emergence began from the March plantings when soil temperatures at a depth of 5 cm reached 17 C. Although the initial growth of March, April, and May plantings was very slow, these plantings eventually produced about 60% more dry matter (2100 g/m2) than June, July, and August plantings (1300 g/m2) when harvested in December. At 8 weeks after planting, June to August plantings accumulated 120% more dry matter (460 g/m2) than March to May plantings (210 g/m2). At 12 weeks, dry matter accumulation was greatly reduced by shorter photoperiods and cool temperatures for March and September plantings (160 g/m2) when compared to all intermediate plantings (700 g/m2). All plantings, except October, produced rhizomes (15 to 120/m2) and seeds (154 to 73400/m2) before killing frosts occurred in late November. Although rhizomes and seeds were not collected until the 12-week harvest for the March to May plantings, these plantings produced or tended to produce the greatest number of rhizomes (85/m2) and seeds (49300/m2) by December. Rhizomes and seeds from the June to September plantings were collected within 8 weeks, indicating that declining photoperiods hastened rhizome and seed production.

Black nightshade plants were controlled by hoeing in the same cotton plots each year (1982 to 1986) for 3 to 15 weeks after crop emergence to evaluate the influence of several black nightshade-free periods on cotton yield, reproduction of black nightshade, and longevity of weed seeds in soil. Similar information, although limited, was also collected for Palmer amaranth that escaped the initial herbicidal treatment each year. Except for 1982, black nightshade competing with cotton for the duration of the growing season in nonhoed plots severely reduced yields (60 to 100%), with greatest yield reductions (82 to 100%) occurring in 1983 and 1984 when 0.5 to 0.7 cm of rain fell within 10 days after cotton planting. When combined with cultivation, a 3-week nightshade-free period at cotton planting was of sufficient duration to protect cotton yields. Weed seed production for all hoed treatments was less than 1% of the nonhoed treatment, and after five consecutive cotton crops (1982 to 1986), the amount of both black nightshade and Palmer amaranth seeds in soil was similar for all hoed treatments. These populations were 60 to 80% and 95 to 97% less than beginning populations of black nightshade and Palmer amaranth in 1982, respectively. After 5 yr of continuous treatments, cotton was grown in 1987, with standard cultivation as the only method of weed control, to evaluate how the weed-free periods in 1982 to 1986 influenced weed seed populations in the soil and the resultant effect on weed competition and cotton yields. Reduction of cotton yields in 1987, in the absence of weed-free periods, indicated that black nightshade seed survival in soil appears to be sufficiently long for ample establishment of this weed to compete with cotton. Thus, fields will have to be kept weed free for greater than 5 yr to reduce black nightshade populations to a level that will not reduce cotton yields.

The effects of bristly starbur interference with peanuts were studied from 1980 through 1983 on a Dothan sandy loam (Plinthic Paleudults). Peanut seed yields, which included kernels plus hulls, were reduced as bristly starbur densities increased from 2 to 64 plants/7.5 m of row. Full-season interference from 8, 16, 32, and 64 bristly starbur plants/7.5 m of row reduced peanut seed yields 14, 26, 43, and 50%, respectively. The seed yield of peanuts maintained weed free for 6 weeks after crop emergence was reduced by no more than 3% compared to peanuts maintained weed free for the entire season. Weed interference for 2 weeks after crop emergence reduced seed yield by an average of 4% over the 3-yr period, based on prediction equations. Bristly starbur interference for 13 weeks after crop emergence reduced peanut forage dry weight yield by 54%. Similarly, peanut interference for 13 weeks after emergence reduced bristly starbur forage dry weight yield by 32%. Bristly starbur density in the forage dry weight studies averaged 35/7.5 m of row. These bristly starbur were confined to a 35-cm band over the drill. Peanut density averaged 72/7.5 m of drill.

Sulfometuron, when applied as a foliar and/or soil application, prevented regrowth of bahiagrass. Sulfometuron application did not reduce regrowth of centipedegrass regardless of method of application. Sulfometuron was absorbed by the roots and foliage of centipedegrass and bahiagrass. Symplasmic translocation of the herbicide was evident in both species. Translocation of foliar-applied sulfometuron increased from approximately 1% at 48 h after application to 23% at 72 h in bahiagrass. Metabolism of sulfometuron was greater in centipedegrass (69% of foliar-applied, 10% of root-applied) at 72 h after application than in bahiagrass (30% of foliar-applied and 4% of root-applied). Tolerance of centipedegrass to sulfometuron appeared to be related to a high degree of herbicide metabolism in this species.

The relationship between trifluralin dosages detected in the soil at seeding, initial crop injury, and subsequent recovery of spring wheat during the growing season was investigated in field experiments in 1986 and 1987. As the amount of trifluralin in the soil increased, both crop density and dry matter production decreased such that at 1 kg/ha the two were reduced by 37 and 50%, respectively, early in the season. As the season progressed, crop growth rates (CGRs) of wheat in trifluralin-treated plots exceeded those of wheat in the untreated plots. Maximum CGRs occurred between Zadok's growth stages 30 and 45 where trifluralin levels in the soil were 0.3 to 0.5 kg ai/ha at seeding. Recovery from trifluralin injury was characterized by enhanced net assimilation rates of surviving plants, increased tillering and greater dry matter production per plant. Wheat seed yield was only weakly correlated with trifluralin levels in the soil at seeding. From a linear regression model it was determined that a 35% reduction in plant dry weight from the trifluralin injury at the beginning of tillering would result in no more than a 10% reduction in seed yield at final harvest.

Cotton and pitted morningglory emergence and dry weight decreased approximately 60 to 80% when these plants were grown under greenhouse conditions in the presence of increasing amounts (0.8 to 6.7 mg debris/g soil) of field-grown crimson clover or hairy vetch debris incorporated into the soil medium. Conversely, corn dry weight increased 20 to 75% when legume debris was placed on the soil surface; incorporated debris had very little effect on corn emergence or dry weight. Germination and seedling growth of corn, Italian ryegrass, cotton, pitted morningglory, and wild mustard decreased progressively, with species-dependent variation, when exposed to increasing concentrations (8.3 to 33.3 g debris/L) of aqueous crimson clover and hairy vetch extract. Mustard and ryegrass germination and growth were almost completely inhibited by full-strength extracts of both legumes. Bioassay species exhibited greater phytotoxic responses to hairy vetch than to crimson clover in the debris and extract studies. Emergence and growth of corn and cotton were not affected when planted into soil samples, containing root biomass and possible leaf and root exudates, collected from beneath field-grown hairy vetch and crimson clover plants. However, morningglory dry weight increased 35% in the presence of either legume root debris and accompanying soil.

Surgical experiments were conducted on cultured five-node apical rhizome segments of quackgrass. Removal of scale leaves promoted an initial burst of growth within the axillary buds but did not support the continued growth of buds as effectively as removal of the rhizome apex. Replacement of detached scale leaves over denuded buds temporarily repressed the promotive effect of scale leaf removal. Aqueous extracts of scale leaf material inhibited apical growth in rhizome segments but did not inhibit bud growth. Anatomical sections revealed that removal of scale leaves promoted development of buds: cells enlarged, vascular tissues differentiated, and new nodes began to form within 4 days of the removal of scale leaves. It is suggested that scale leaves contribute to apical dominance by inhibiting the initial development of axillary buds.

The phytotoxicity of the butyl ester of fluazifop to quackgrass was enhanced by the addition of a nonionic surfactant and an oil additive either alone or in mixture to the spray solution. The enhancement caused by the surfactant was consistently greater than that caused by the oil additive. A higher level of quackgrass control was achieved at the carrier volumes of 100, 200, or 400 L/ha, than at 800 L/ha. Quackgrass growth inhibition was greater following application of small herbicide droplets which averaged 0.25 μl compared to larger herbicide droplets at each herbicide application rate. When droplet concentration was varied and different doses of the herbicides applied to plants, no significant differences were noted at the highest dose. However, at intermediate dose treatments, the least concentrated droplets (2.5 μg/μl) were most phytotoxic. Herbicide droplets placed at basal areas of leaves were more phytotoxic than when placed at lamina apices and middle areas. This effect was most pronounced on adaxial rather than abaxial surfaces. In general, application of droplets to younger leaves resulted in greater phytotoxicity than treatment of older leaves.

Dormant barnyardgrass seeds imbibed in darkness for 8 days at 38 C displayed a very low fluence response to phytochrome, and very little germination occurred in darkness. However, if seeds were imbibed at temperatures >42 C or exposed to 46 C for only 0.5 h, considerable germination was evoked in the absence of a light stimulus. It is proposed that the high temperatures caused a transition in dormancy from a light-requiring to a light-independent state. The finding may have relevance to field behavior of barnyardgrass seeds where burial could prevent reception of the required light stimulus.

Establishment of seedlings of big sagebrush subsequent to range weed control treatments limits the economic feasibility of such treatments for increased forage production. This study investigated the dynamics of seed production by this species as one step in understanding seedling establishment. Studies were conducted on five different ecological sites along the arid extremity of big sagebrush distribution in western Nevada. Demography, physical dimensional parameters, biomass, and community structure were determined for each site and related to seed production over a 4-yr period. In addition, seeds harvested from each site were used to grow plants that were transplanted to establish reciprocal gardens at all sites. Seeds were subsequently harvested from the plants in these gardens. The average stand studied was capable of producing about 50 million seeds/ha annually. The plant characteristics most closely correlated with seed production were leaf weight, canopy density, and root crown diameter. The stand that consistently had the highest average seed production had the lowest woody biomass accumulation rate. In reciprocal gardens, plants grown from this stand had the highest average seed production. Seed production of big sagebrush plants appears to be related to site characteristics, shrub biomass characteristics, and inherent genetic potential of the plants in a given collection.

The purpose of this study was to investigate seed dispersal and germination of seeds in the soil as factors in establishment of big sagebrush seedlings. Seed dispersal began at seed maturity in December. Under the shrub canopy the dispersal of seeds was greater to the east. Between shrubs the dispersal of seeds tended to be uniform. For 6 months of each year there were no detectable germinable seeds in the litter and surface soil at the sites sampled. Germinable seeds in the soil increased rapidly during seed dispersal but were not detected by June of the next season. Enrichment of bioassay samples with GA3 or KNO3 did not enhance emergence of big sagebrush seedlings. Big sagebrush seedlings were found at very low densities in areas previously burned in wildfires. This suggests the presence of viable big sagebrush seeds in the soil at a very low density.

Competitive interactions of wheat and wild oats in relation to variations in plant density of both species were investigated in field studies under irrigation and added fertilizer. Competition studies included comparisons by both additive and replacement series. The additive series was used to study plant responses to competition under fixed density of wheat and increasing density of wild oats. The replacement series was used to study plant responses to competition under constant total plant density with differing proportions of wheat and wild oats. On a per plant basis, shoot dry weight and leaf area index of wild oats were less than those of wheat at anthesis. However, the replacement series experiment indicated that wheat and wild oats were equivalent in competitiveness. Relative density of wild oats gave a better regression fit for wheat yield than did absolute wild oats density (r2 values of 0.83 and 0.61, respectively). Yield of wheat grain was linearly proportional to relative density of wild oats.

Replacement studies were conducted under greenhouse conditions to determine if available soil water influences the competitive interaction between soybean and Florida beggarweed. Stomatal conductance and leaf water potential were determined for both species under different levels of available soil water to identify possible mechanisms involved in changes in the relative competitiveness induced by the water deficits. Soybean leaf area and aboveground biomass were greater than for Florida beggarweed under optimum water, but equal to or less than Florida beggarweed with water stress. Soybean was more competitive than Florida beggarweed when there was adequate soil water but less competitive than Florida beggarweed under water stress. Stomatal conductance was higher for soybean with optimum soil water (at high leaf water potentials) but equal to Florida beggarweed as soil water became limiting (low leaf water potentials). These data indicated that water stress differentially affected soybean and Florida beggarweed.

Several weed-free and johnsongrass competition periods were established and maintained in cotton to evaluate their influence on cotton yield and reproduction of johnsongrass. When johnsongrass was sprayed with fluazifop in field plots 3, 6, 9, or 12 weeks after cotton emergence, only plots sprayed at 3 weeks yielded as much cotton as weed-free plots. Johnsongrass permitted to compete for 6, 9, 12, and 25 weeks reduced cotton yields 20, 60, 80, and 90%, respectively. When johnsongrass was transplanted into weed-free plots 3, 6, 9, and 12 weeks after cotton emergence, a weed-free period of 9 weeks was required to prevent significant cotton yield reduction. Cotton in plots weed free for 3 and 6 weeks yielded 81 and 89% as much seed cotton, respectively, as weed-free controls. Johnsongrass competing with cotton for 9 to 12 weeks produced 20 and 40% as many seeds and rhizomes, respectively, as weedy control plots. Some seeds and rhizomes were produced (1% of weedy check plots) in plots weed free for 9 to 12 weeks. Cotton grades were reduced in plots weed free for 3 and 6 weeks, and in plots where johnsongrass competed for 9 to 25 weeks.

The effects of hogpotato interference on cotton and of the crop on the weed were measured under field conditions in four environments. Full-season interference from 105 ± 21 hogpotato plants/m2 reduced cotton plant height by 14 to 44%. Conversely, weed dry weight was reduced 54% through full-season interference from cotton. Lint yield reductions in cotton ranged from 31 to 98% following full-season weed interference. Interference during the first 7 weeks of crop growth reduced lint yield by approximately 40%; however, interference after 7 weeks of weed-free maintenance did not affect lint yield. Interference reduced boll size in 3 of 4 yr, lint percent in 2 of 4, and boll number in the only year it was measured. Cotton fiber length, uniformity index, and micronaire were reduced by full-season interference in 1 of 2 yr; however, fiber strength was not affected in either year. Significant use of soil water by hogpotato occurred at 120 cm and deeper in the soil while cotton used water primarily in the upper 75 cm.

Florida beggarweed seeds were collected in Georgia, Florida, and South Carolina from plants differing in morphological characteristics. Seedlings were transplanted into peanut rows in field studies at Tifton, GA, and Jay, FL, in 1986 and 1987, and frequent observations of vegetative and reproductive characteristics were made. The competitiveness of the Florida beggarweed selections was evaluated by comparing pod weights from peanut plants grown in rows adjacent to the individual weed selections with pod weights of weed-free peanuts. There were significant differences among selections of Florida beggarweed in days to maximum height, maximum node formation, maximum branching, and initial flowering and fruiting at both locations. Selection GA-1 generally reached these growth stages earliest, was shorter, narrower, had fewer nodes, and produced less dry matter and fewer seeds than GA-2, which was generally the latest maturing selection. GA-4 produced fewer branches and smaller seeds than the other selections. Peanut pod weights adjacent to Florida beggarweed plants were reduced 12 to 18% in 1986 and 10 to 24% in 1987 compared to weed-free checks. Florida beggarweed selection GA-2 was the most competitive and GA-4 was among the least competitive both years. The variation of measured parameters among Florida beggarweed selections in this study may contribute to the survival and adaptability of this weed with changing environmental conditions, cultural practices, and control measures.

Morphological and physiological variation among annual bluegrass populations from the green, fairway, and rough were measured to determine the role annual bluegrass infestations outside the green play in maintaining the population in the green. Annual bluegrass populations from the fairway and the rough were similar to each other but differed from that of the green in habit, dry mass production, flowering, seed size, and germination. Seeds from each population established best in the type of turf from which they originated. It is concluded that, since few genotypes were common to the green and its surroundings, the populations in the fairway and rough played little or no role in maintaining the population of the green. The same is likely to be true wherever the management of greens and their surroundings differs sufficiently for marked population differentiation to occur. This finding does not preclude the possibility that some genotypes adapted to the green persist in the surroundings, and that these genotypes serve as sources of seeds for the colonization or reinfestation of annual bluegrass-free greens.

Fresnel lenses are used to concentrate solar radiation to a line or point. A linear Fresnel lens (0.91 by 1.52 m, 0.74-m focal length, 0.01- by 1.52-m line focus) was investigated as a method for weed control. Field experiments were conducted to assess the effect of Fresnel lens concentrated solar radiation at various exposure times, stages of plant growth, and soil surface moisture conditions. On a dry soil surface exposure times of 1 to 10 s at 290 C resulted in control of redroot pigweed from 100% for a 1-s exposure at the cotyledon stage to 89% for a 10-s exposure at the 10-leaf stage. Redroot pigweed and kochia control was similar at exposures of 3 to 10 s, but less for kochia at 1 and 2 s. Green foxtail control was less than that of kochia and redroot pigweed. Control was reduced on a moist compared to a dry soil surface. Concentrated solar radiation holds the greatest potential for control of small dicot weeds on a dry soil surface.