Infestations of common milkweed (Asclepias syriaca L.), in descending order of incidence in Nebraska, occurred on areas occupied by soybean [Glycine max (L.) Merr.], oats (Avena sativa L.), sorghum [Sorghum bicolor (L.) Moench.], railroad rights-of-way, fallow land, roadsides, corn (Zea mays L.), winter wheat (Triticum aestivum L.), pasture, and alfalfa (Medicago sativa L.). Average crop yield reductions, within common milkweed communities of 11100 to 45 200 plants/ha, ranged from 2 to 10% for corn, 4 to 29% for sorghum, and 12 to 19% for soybeans. Reductions in crop yields tended to increase with increasing common milkweed populations. Germination percentage of common milkweed and sorghum were not significantly affected by growing medium conductivities below 7 and 13 mmho/cm2, respectively. Growth media at pH 2 significantly reduced germination percentage, hypocotyl length, and radicle length of both common milkweed and sorghum as compared with pH 4 to 10. Undiluted aqueous extracts of common milkweed shoot and root material significantly reduced germination percentage, hypocotyl length, and radicle length of sorghum.

A better understanding of the persistence of jointed goatgrass seed in soil and its dormancy will lead to the development of more effective weed-management strategies. Three populations of jointed goatgrass were collected from winter wheat fields in Oregon, and grown together with the winter wheat variety ‘Madsen’ in nurseries at Moro and Pendleton, OR. Germination responses of jointed goatgrass and wheat seed were recorded over 14 d at 5/5, 15/10, 15/15, 25/15, 25/25, and 30/20 C day/night temperatures and a 12-h photoperiod. Because jointed goatgrass spikelets often contain two seed, primary and secondary seed germination values were recorded. Secondary seed germination was defined as 3-mm radicle protrusion, and primary seed germination was defined as 5-mm emergence of the second coleoptile. Jointed goatgrass secondary seed germinated when exposed to all temperature regimes. Jointed goatgrass secondary seed germination occurred 3 d earlier in temperature regimes involving 15 C compared to germination at 5/5, 25/25, and 30/20 C. Final germination values for jointed goatgrass secondary seed were greatest when seed were incubated at 25/15 C. Wheat seed germinated at all temperature regimes, although the onset of germination occurred 1 to 1.5 d later at 5/5 C compared to other temperature regimes. Jointed goatgrass primary seed germinated only at 15/10, 15/15, and 25/15 C, and maximum germination occurred at 25/15 C. Dormancy in jointed goatgrass might prevent germination of seed within freshly shattered spikelets until autumn when temperatures are low and moisture is available. Because final germination percentages in jointed goatgrass primary and secondary seed were less than 100%, additional research on factors regulating dormancy is needed.

A pot bioassay, based on root growth of pregerminated corn, was used to evaluate factors influencing field persistence of chlorsulfuron, metsulfuron, triasulfuron, and tribenuron, which were applied preemergence at 0, 10, 20, and 40 g ai ha−1 to wheat grown in three soils that differed in texture (sandy loam, sandy clay loam, and silty clay loam) and pH (7.9, 4.7, and 7.6). Residual activity and leaching of all herbicides in all soils increased with increasing rate of application, with the exception of tribenuron which showed practically no residual activity and leaching in sandy clay loam soil. Sunflower sown 4 mo after tribenuron application in all soils was not injured by any rate used but was significantly affected by the other herbicides. Lentil and sugarbeet also were affected by all herbicides in all soils. These three crops sown 8 mo after herbicide application were not affected by any herbicide used in the sandy clay loam soil but were injured by chlorsulfuron, triasulfuron, and metsulfuron in the sandy loam soil. Only lentil and sugarbeet were injured by chlorsulfuron in the silty clay loam soil.

Trifloxysulfuron controls green and false-green kyllinga more effectively than halosulfuron. Studies were conducted to evaluate the absorption, translocation, and metabolism of 14C-halosulfuron and 14C-trifloxysulfuron when foliar applied to green and false-green kyllinga. No differences were observed between the two kyllinga spp. with regard to absorption, translocation, or metabolism of either herbicide. The majority of 14C-halosulfuron and 14C-trifloxysulfuron was absorbed by 4 h, with an accumulation of 63 and 47% radioactivity, respectively. Accumulation of both herbicides occurred in the treated leaf and the primary shoot from whence the treated leaf was removed, with minor accumulation occurring in the roots and newly formed rhizomes. Of the total amount of 14C-halosulfuron absorbed into the plant, 77% remained in the form of the parent compound compared with 61% of 14C-trifloxysulfuron. The parent compound was distributed mainly in the treated leaf and primary shoot, whereas polar metabolites were concentrated in the roots and rhizomes. Nonpolar metabolites of 14C-trifloxysulfuron accumulated in the treated leaf and primary shoot. These data indicate that absorption, translocation, or metabolism could not explain the variation in green and false-green kyllinga control between halosulfuron and trifloxysulfuron.

‘Mars’, ‘Lemont’, and ‘Tebonnet’ rice were treated in 1987 and 1988 with fenoxaprop, sethoxydim, and haloxyfop at 3- to 4-leaf preflood and at panicle initiation postflood growth stages. Rice stunting and stand loss generally were greater from herbicides applied at postflood than at preflood with all cultivars. Mars yields were reduced from 11 to 23% by fenoxaprop at 168 and 336 g ha−1 applied preflood or postflood. Only postflood applications of fenoxaprop reduced Lemont and Tebonnet yields. Sethoxydim at 112 and 224 g ai ha−1 reduced yields of all cultivars when applied postflood, but yields were not reduced with preflood applications. Haloxyfop preflood at 140 g ai ha−1 and postflood at 70 and 140 g ai ha−1 reduced yields of Mars both years compared to the untreated control. Yields for Lemont and Tebonnet were reduced both years only when haloxyfop was applied postflood at 140 g ha−1.

Field experiments were conducted in 1985 and 1986 under eight environments to evaluate the population dynamics of a range of silverleaf nightshade densities and to measure the effects of those populations on cotton lint yield. Dry weed weights of silverleaf nightshade stands were influenced by growing conditions among years, but were positively related to initial densities as long as 2 yr after establishment. Stem numbers increased as initial densities and stand age increased. A negative linear relationship existed between cotton lint yield and weed biomass and between cotton lint yield and stem number from both 1- and 2-yr-old weed stands. For each 1 kg/10 m of row increase in dry weed weight from 1- and 2-yr-old stands, a 9 and 21% lint yield loss/ha was predicted, respectively. For each stem/10 m of row, a 0.35 and 0.31% yield loss was predicted, respectively. Late-planted cotton was less vulnerable to yield reductions by silverleaf nightshade; however, its yield potential was also less.

The tolerance of bermudagrasses ‘Tifway’, ‘Tifgreen’, ‘Tifdwarf’, ‘Ormond’, and ‘Floraturf’ [Cynodon dactylon (L.) Pers.] cultivars to repeated annual applications of oxadiazon [2-tert-butyl-4-(2,4-dichloro-5-isopropoxyphenyl)-Δ2-1,3,4-oxadiazolin-5-one] and butralin [4-(1,1-dimethylethyl)-N-(1-methylpropyl)-2,6-dinitrobenzenamine] were evaluated over a 4-yr period. Oxadiazon treatments did not affect growth characteristics of these bermudagrasses. Butralin caused moderate to severe reduction in sod density. ‘Tifway’, ‘Ormond’, and ‘Floraturf’ were more tolerant to butralin than ‘Tifgreen’ and ‘Tifdwarf’.

Replacement series and growth analysis experiments under greenhouse and field conditions quantified and explained the competitive ability of wild oats and barley. Barley was a stronger competitor than wild oats under greenhouse and field conditions. The reciprocal yield approach showed that barley's intraspecific competition was 7.3 times greater than its interspecific competition with wild oats when calculated on a dry weight per plant basis. When leaf area per plant was the yield variable, barley's intraspecific competition was only 2.4 times greater than its interspecific competition. The difference was explained by wild oats' higher leaf area ratio. Barley had a greater leaf area, root and shoot biomass, absolute growth rate, and shoot-root ratio than wild oats, but wild oats' leaf area ratio was always higher. No differences were detected in relative growth rate and net assimilation rate.

Growth and regeneration of field horsetail (Equisetum arvense L. ♯ EQUAR) were investigated under field and greenhouse conditions. Field horsetail produced shoots during the entire summer but its growth was detrimentally affected by the presence of corn (Zea mays L.). Field horsetail regrew as well whether it had been hoed once or 16 times during the growing season; and during the subsequent summer, there were no significant differences between horsetail growth in plots kept weed-free the previous growing season and in plots where field horsetail grew freely. In the greenhouse, rhizome segments 1 cm long placed 15 cm deep easily regenerated plants. Simulations were done using the growth and regenerative ability of field horsetail to estimate its potential spread in agricultural fields. The results of these simulations indicate that this weed can infest a hectare within 6 yr of its introduction into a new area.

Soil samples representing a time series from forest before clearing to land in cultivation for 20 yr were taken near Delta Junction, AK, to determine the changes that occur in the soil seed bank following clearing and agricultural use. The total number of seed was initially low in the forested sites but increased after 3 to 5 yr in cultivation due to seed production by native colonizers and by introduced weeds such as common lambsquarters (Chenopodium album L. ♯3 CHEAL). Viability of seed of several mature forest species was low. There was a shift from a seed bank dominated by native species in the forest and newly cleared sites to a seed bank dominated by introduced colonizers in the older fields. Although seed of introduced species increased in importance over time, native species, especially native colonizers, continued to be an important component of the seed bank throughout the 20-yr period represented.

Seed were harvested from soybean [Glycine max (L.) Merr. ‘Cutler’] plants treated at flowering and pod filling with (2,4-dichlorophenoxy)acetic acid (2,4-D), 4-(2,4-dichlorophenoxy)butyric acid (2,4-DB), and 3,6-dichloro-o-anisic acid (dicamba). Progeny of plants treated at flowering with 2,4-D and 2,4-DB or at pod filling with the lowest rate were normal. When higher rates were applied at pod filling, these phenoxy herbicides caused appreciable injury to the progeny in the form of reduced emergence and dry weight and malformed unifoliate leaves. Dicamba was much more injurious to the progeny of treated plants than 2,4-D and 2,4-DB. Even at low rates dicamba caused reduced germination, emergence, and dry weight and malformed first trifoliate leaves.

Understanding spatial distribution has become increasingly important in weed science. Seed dispersal, both between and within agricultural fields, is an important component of weed spatial distribution. Analysis of the effect of dispersal between fields has been relatively neglected in theoretical studies of weed population dynamics. In this paper, we present a simple landscape-level model of the influence of seed dispersal on winter wild oat population dynamics between fields. In the model, two fields are interconnected, with seeds being carried from one field to another as would occur when seeds are carried by field equipment or in irrigation water. The model is intended to characterize the effect of field-level weed management decisions on landscape-level weed population dynamics. Three scenarios were studied. The first employed no control measures in either field. The second employed annual application of herbicides in field 1 with field 2 receiving no treatment. In the third scenario, an herbicide application took place in field 1 only if the weed population in that field exceeded an action threshold. In the first scenario, the net result of the immigration and emigration processes determined the increase or decrease of the stable plant population. In the second scenario, weeds in the controlled field (field 1) were not driven to extinction as might be expected. The weed populations grew for practically all the dispersal parameter space. Each change in the parameter's values produced a new stable equilibrium. This situation might correspond to a multiplicity of stable states. The uncontrolled field (field 2) experienced an indirect control effect due to the use of control measures in field 1. In the third scenario, we observed an interesting behavior of the populations in both fields. The population in field 1 was not driven under the economic threshold, and both fields showed complex dynamics within defined combinations of migration and emigration values.

Among 12 of the more effective surfactants selected from a preliminary experiment, there were few differences in their ability to increase atrazine toxicity to large crabgrass [Digitaria sanguinalis (L.) Scop.] and sorghum (Sorghum vulgare Pers.), or in toxicity to large crabgrass and sorghum when used alone. Surfactants per se showed some toxicity to large crabgrass and sorghum. As large crabgrass increased in size, it became less susceptible to injury from atrazine plus dodecyl ether of polyethylene glycol (Surfactant WK). Early spraying with atrazine plus Surfactant WK reduced the top-growth yield of six grass species.

In field studies, atrazine alone and surfactants plus atrazine applied at the 1-in weed height gave very good early weed control. Field plots treated at the 4-in weed height generally produced more weed top-growth and less sorghum than plots treated at the 1-in height. Only the preemergence atrazine treatments gave weed yields that were equal to treatments that included handweeding. Sorghum injury from the surfactants was evidenced by reduced stover yields.

Atrazine plus surfactant toxicity to emerged large crabgrass, grown in growth chambers, increased with higher relative humidities. This was not true for sorghum. The 1% surfactant mixtures generally had a lower surface tension than the 0.1% concentrations although the differences were not great. Surface tension was not the main factor governing the phytotoxicity of foliar-applied atrazine solutions. Translocation of atrazine from sorghum and large crabgrass leaves dipped in a C14-ring-labeled atrazine solution was very slight or nonexistent.

The sensitivity of giant duckweed (Spirodela polyrhyza (L.) Schleid), common duckweed (Lemna minor L.), Wolffiella floridana (Smith) Thomp., azolla (Azolla caroliniana Willd.), and watermeal (Wolffia columbiana Karst.) to diquat (6, 7-dihydrodipyrido [1,2-a:2’,1′-c] pyrazidiinium salt) and paraquat (1,1′-dimethyl-4,4′-bipyridinium salt) was in that order (most to least sensitive). The rapidity of chlorosis in giant duckweed was directly related to the light intensity. The light quality having the most effect on the activity of diquat and paraquat on duckweed was red (600+ millimicrons), and green (510–560 millimicrons) had the least effect.

A growth cabinet study was conducted to evaluate the effect of temperature on the distribution of several herbicides in quackgrass. Uniformly labeled 14C-sucrose and the radiolabeled herbicides glyphosate, sethoxydim, cloproxydim, the butyl ester of fluazifop, the methyl ester of haloxyfop, and the ethyl ester of quizalofop were applied to quackgrass grown at three day / night temperature regimes (10/5, 20/15, and 30/25 C). Seven days after treatment the plants were harvested, lyophilized, and later sectioned, mapped, and oxidized in preparation for 14C quantification. Quackgrass rhizome growth was more vigorous at 20/15 than 30/25 or 10/5 C. of the herbicides tested, haloxyfop was the most inhibitory to rhizome growth. Temperature increases from 10/5 to 20/15 or from 20/15 to 30/25 C resulted in more translocation to shoots. Increasing temperature had various effects on translocation to rhizomes depending on the chemical applied. At all three temperature regimes, more 14C was recovered from distal than basal buds in plants treated with 14C-sethoxydim. In contrast, at all three temperature regimes, similar amounts of 14C were recovered from the distal and basal buds of plants treated with 14-C-sucrose.

Twelve analogs of the strigol D-ring (butenolides) were evaluated at 0.1 mM as germination regulators of 26 weed and crop seeds. In general, the butenolides either inhibited or did not affect monocot germination, although the hydroxybutenolide stimulated germination of dormant cheat and nondormant perennial ryegrass and sorghum seeds. The response rate for dicots was greater but still primarily inhibitory. Dormant lettuce seeds (both light-sensitive and light-insensitive), Palmer amaranth, and redroot pigweed showed several significant responses, both inhibitory and stimulatory. Some of the butenolides that had not been previously assayed against witchweed were tested as 10-4 to 10-11 M dilution series. The allyloxybutenolide demonstrated activity comparable to strigol (30 to 60% germination at 10-6 to 10-11 M); the sec-butyloxybutenolide was somewhat less active (20 to 40% germination) but still effective at 10-9 M. In general, the butenolide analogs of strigol were less effective in stimulating seed germination than the multiring analogs.

Field and greenhouse experiments were conducted to observe and measure the phytotoxicity of glyphosate [N-(phosphonomethyl)glycine] to potatoes (Solanum tuberosum L. ‘Russet Burbank’) applied at different stages of growth and to determine if glyphosate was translocated into the original mother tuber (seed piece) prior to initiation of daughter tubers. Glyphosate injury symptoms appeared 1 day after treatment and at least 50% of the foliage was necrotic within 7 days. Significant decreases in plant height, shoot and root dry matter content, and daughter tuber production were recorded at the 0.28- and 0.56-kg/ha rates. Higher rates of 1.12 and 2.24 kg/ha did not give further significant reductions. Maximum levels of 14C activity accumulated in all plant parts 4 days after application of the 14 C-glyphosate. The 14 C-glyphosate accumulated primarily in the apical meristem and roots. Extremely low levels of 14 C activity were detected in the mother tuber regardless of plant age when treated. Phytotoxic effects on the eyes of the mother tuber increased in severity with increasing rates of glyphosate as evidenced by abnormal sprouting.

Long-term absorption of 14C-atrazine [2-chloro-4 - (ethylamino) - 6 - (isopropylamino) - s - triazine] by excised velvetleaf (Abutilon theophrasti Medic.) roots was investigated. A rapid, initial phase of absorption was followed by a long-term, linear phase of absorption, which resulted in atrazine accumulation in the tissue to concentrations above the external solution. This accumulation did not result from metabolism of the atrazine. Aging of the excised tissue appeared to be responsible for the accumulation. Dinitrophenol, but not cyanide, inhibited accumulation. Atrazine accumulation decreased as the temperature during absorption was decreased. The Q10 the absorption rate was ca. 2.5 between 15 and 25 C. Efflux of atrazine from the tissue occurred in two phases. At 25 C, loss of 80% of the atrazine occurred in 20 min. At 4C, the rate of this efflux was slower and the phase lasted longer. At both 4 and 25 C a second, slower phase of efflux occurred through at least 6 h and resulted in loss of equal amounts of atrazine at the two temperatures. These experiments show that, in addition to rapid absorption of atrazine to a passive equilibrium, excised velvetleaf roots accumulate atrazine by a metabolically dependent process over long periods of time.

Growth and reproductive potential of individual yellow nutsedge plants were examined under two nitrogen levels and three soil moisture regimes. Irrigation levels were selected on the basis of irrigating at soil water potentials of −20, −50, and −80 kPa. Yellow nutsedge patch expansion was measured using digital images to determine ground cover, while plots were subsampled to estimate total shoot and tuber production. High nitrogen increased shoot production in 2004. When plots were irrigated at a soil water potential of −20 kPa, a single yellow nutsedge plant produced 3,000 and 1,700 shoots and 19,000 and 20,000 tubers in 2003 and 2004, respectively. Patch expansion at −20 kPa was exponential, with the greatest expansion occurring between the middle of July and mid to late August. This research demonstrates that the vegetative and reproductive potential of yellow nutsedge is greatly influenced by irrigation level. With such extensive growth and reproductive potential, management strategies for yellow nutsedge should focus on prevention, early detection and containment, early treatment, and integration of control strategies to reduce its competitiveness and spread.

Striga hermonthica reduces cereal yields in large areas of sub-Saharan Africa. Recent research has shown that transplanting maize seedlings that are more than 15 d old reduced Striga emergence and improved crop yields. Field experiments were conducted in 1998 and 1999 to determine whether maize varieties with different maturity periods and susceptibility to Striga parasitism respond similarly to transplanting. There was a considerable difference in Striga emergence between varieties in direct-seeded maize, but transplanting clearly reduced Striga emergence for all varieties. Transplanting of maize in plastic tubes gave the best Striga control until 8 wk after transplanting, whereas transplants from nurseries provided better season-long control. Transplanting improved grain yields 50 to 100% compared with direct seeding for three of the four varieties tested. Only the early-maturing variety ‘Morogoro’ had lower yields with transplanting than with direct seeding, indicating that transplanting caused more stress on the plants than was alleviated by the lower Striga infestation. The two varieties (‘Pioneer 3251’ and ‘H622’) most susceptible to Striga parasitism profited the most from transplanting, and the concomitant reduction in Striga induced stresses. Increases in productivity because of transplanting were associated with increases in biomass or harvest index. Transplanting of different maize varieties under rain-fed conditions has proven to be a biologically efficient method to improve maize yield and reduce Striga infestation within one season.