Greenhouse experiments were conducted to determine the effect of mixing bromoxynil with clethodim, sethoxydim, fluazifop-P, fluazifop-P plus fenoxaprop-P, or quizalofop-P on annual grass control. Antagonism with mixtures of bromoxynil and graminicides was dependent upon species and the graminicide in the mixture. Goosegrass control was unaffected by mixing bromoxynil with any graminicide. Mixing bromoxynil with clethodim, sethoxydim, fluazifop-P, or fluazifop-P plus fenoxaprop-P had no effect on control of Texas panicum, but the rate of quizalofop-P required for 80% control was increased 240%. Mixing bromoxynil with clethodim or sethoxydim had no effect on control of large crabgrass or yellow foxtail, but the rate of fluazifop-P, fluazifop-P plus fenoxaprop-P, or quizalofop-P required for 80% control was increased 180 to 290%. Antagonism of large crabgrass and yellow foxtail control with mixtures of quizalofop-P and bromoxynil increased as the rate of bromoxynil increased. Antagonism toward large crabgrass and yellow foxtail was alleviated by applying bromoxynil 6 d before the graminicides or 3 or 6 d after the graminicides.

Field experiments were conducted on eight weed species to determine if chlorimuron, fomesafen, imazethapyr, or sulfentrazone at two rates (labeled and one-half the labeled rate) were complementary tank mixtures with glyphosate at 210 and 420 g ai ha−1. Laboratory experiments were conducted on barnyardgrass, pitted morningglory, Palmer amaranth, and velvetleaf using radiolabeled glyphosate, chlorimuron, and imazethapyr to determine the absorption and translocation pattern of these herbicides applied alone and in combination. In the field, glyphosate plus chlorimuron tank mixtures were generally additive. Adding chlorimuron did not decrease absorption or translocation of 14C-glyphosate by barnyardgrass, pitted morningglory, or velvetleaf. Adding glyphosate increased absorption of 14C-chlorimuron by Palmer amaranth and velvetleaf. All four fomesafen plus glyphosate rate combinations were antagonistic to goosegrass, sicklepod, Palmer amaranth, and velvetleaf, and three of the four were antagonistic to barnyardgrass and entireleaf morningglory. Fomesafen decreased absorption and translocation of 14C-glyphosate in barnyardgrass, pitted morningglory, and velvetleaf. Ninety percent of glyphosate plus imazethapyr combinations were additive or synergistic, with all rate combinations synergistic for pitted morningglory. Adding glyphosate to imazethapyr increased absorption of 14C-imazethapyr by Palmer amaranth and velvetleaf. Glyphosate plus sulfentrazone tank mixtures were antagonistic at all rate combinations for barnyardgrass and Palmer amaranth and at three of the four combinations for goosegrass and entireleaf morningglory, indicating that these herbicides are not complementary in tank mixtures.

Weed control by heat or flaming typically uses flames to burn small weeds, directed away from desired crops. This research studied an enclosed flaming system for weed control before turfgrass establishment. Field research trials were conducted to explore the efficacy of a PL-8750 flame sanitizer at two application timings. Treatments included various application methods of PL-8750 flame sanitizer and common thermal and chemical weed control methods. Data were weed control relative to the control treatment. Species evaluated included carpetweed, Virginia buttonweed, spotted spurge, large crabgrass, goosegrass, old world diamond-flower, cocks-comb kyllinga, and yellow nutsedge. Turfgrass establishment was not successful in summer but was successful in fall. Fall-application timing trials resulted in > 60% tall fescue establishment at 6 wk after seeding (WAS) for all treatments. Summer-application timing trials resulted in unacceptable turfgrass establishment (≤ 18%) for all evaluated turfgrass species at 6 WAS. Broadleaf and grassy weeds were better controlled compared with sedge weeds. Overall, solarization; covered, emerged-weed flaming; and double applications of covered, emerged-weed flaming were the most successful treatments. Solarization controlled carpetweed, Virginia buttonweed, spotted spurge, large crabgrass, and goosegrass > 80% at 6 WAS. Weed control across thermal treatments were equal to or greater than the comparison chemical treatment (dazomet at 389 kg ha−1). Results indicate thermal weed control has potential for reducing weed populations before turfgrass establishment.

The occurrence of glyphosate-resistant weeds has been reported after more than 20 yr of extensive use. Rigid ryegrass that evolved resistance to glyphosate was found in Australia and in California. Glyphosate-resistant rigid ryegrass plants were collected from northern California and selected through generations 8 and 5 to segregate the most resistant (R) and sensitive (S) biotypes. The eighth generation of R and the fifth generation of S biotypes survived 6.72 and died from 0.11 kg ae ha−1 glyphosate, respectively. The objectives of this study were to evaluate the role of metabolism in the observed resistance, to study the effect of glyphosate on the activity of 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS; EC 2.5.1.19), and to characterize the EPSPS gene in R and S rigid ryegrass. Neither quantitative nor qualitative difference was observed in the metabolism of 14C-glyphosate between the biotypes. Activity of constitutive EPSPS decreased more significantly in the S than R biotype in the presence of 5, 50, 500, and 5,000 µM glyphosate. Inhibition of 50% (I50) of the EPSPS activity by glyphosate was more than 90-fold in S compared to R biotype. Decreased EPSPS sensitivity in the R biotype appeared to be a major contributor to glyphosate resistance in rigid ryegrass from California. Fragments of the EPSPS gene containing 1,320 nucleotides were isolated from mRNA of S and R biotypes. A single nucleotide mutation from cytosine (C) to thymine (T) was identified at nucleotide 301 of the truncated EPSPS gene of the R biotype. This mutation changed the amino acid code from proline (Pro) to serine (Ser), which was similar to that reported for the glyphosate-resistant goosegrass from Malaysia and correlated with glyphosate insensitivity of EPSPS.

Few studies on herbicide resistance report data to establish unambiguously the correlation between genotype and phenotype. Here we report on the importance of the EPSPS prolyl106 point mutation to serine (P106S) in conferring resistance to glyphosate in a goosegrass population from Davao, Mindanao Island, the Philippines (Davao). Initial rate-response studies showed clear survivors within the Davao population at glyphosate rates that completely controlled the standard sensitive goosegrass population (STD1). Assessment of potential resistance mechanisms identified the presence of P106S mutant individuals in the Davao population. Polymerase chain reaction (PCR) amplification of specific alleles (PASA) analysis established that the mixed-resistant Davao population was comprised of 39.1% homozygous proline wild-type (PP106), 3.3% heterozygous serine mutant (PS106), and 57.6% homozygous serine mutant (SS106) genotypes. Further rate-response studies on plants with a predetermined genotype estimated the Davao SS106 individuals to be approximately 2-fold more resistant to glyphosate compared to Davao PP106 individuals. Extensive analysis at different goosegrass growth stages and glyphosate rates established strong correlation (P < 0.001) between presence of P106S in EPSPS and the resistant phenotype. Importantly, no differences in the pattern of absorbed or translocated 14C–glyphosate were observed between PP106 and SS106 Davao genotypes or Davao and STD1 individuals, suggesting that glyphosate resistance in the Davao population was attributable to an altered target site mechanism. This study demonstrates that whilst P106S in EPSPS confers a moderate resistance level to glyphosate, the mechanism is sufficient to endow glyphosate failure at the recommended field rates.

Field studies were conducted in five states at six locations from 2002 through 2003 to evaluate weed control and cotton response to early POST (EPOST), POST/POST-directed spray (PDS), and late POST-directed (LAYBY) systems using glyphosate-trimethylsulfonium salt (TM), s-metolachlor, trifloxysulfuron, prometryn, and MSMA. Early POST applications were made from mid May through mid June; POST/PDS applications were made from early June through mid July; and LAYBY applications were made from early July through mid August. Early season cotton injury and discoloration was minimal (< 1%) with all treatments; mid- and late-season injury was minimal (< 2%) except for trifloxysulfuron POST (11 and 9%, respectively). Annual grasses evaluated included barnyardgrass, broadleaf signalgrass, goosegrass, and large crabgrass. Broadleaf weeds evaluated included entireleaf morningglory, pitted morningglory, sicklepod, and smooth pigweed. For the EPOST, POST/PDS, and LAYBY applications, weeds were at cotyledon to 10 leaf, 1 to 25 leaf, and 2 to 25 leaf stage, respectively. Annual broadleaf and grass control was increased with the addition of s-metolachlor to glyphosate-TM EPOST systems (85 to 98% control) compared with glyphosate-TM EPOST alone (65 to 91% control), except for sicklepod control where equivalent control was observed. Annual grass control was greater with glyphosate-TM plus trifloxysulfuron PDS than with trifloxysulfuron POST or PDS, or trifloxysulfuron plus MSMA PDS (90 to 94% vs. 75 to 83% control). With few exceptions, broadleaf weed control was equivalent for trifloxysulfuron applied POST alone or PDS alone or in combination with glyphosate-TM PDS or MSMA PDS herbicide treatments (81 to 99% control). The addition of a LAYBY herbicide treatment increased broadleaf weed control by 11 to 36 percentage points compared with systems without a LAYBY. Cotton lint yield increased 420 kg/ha with the addition of s-metolachlor to glyphosate-TM EPOST treatments compared with systems without s-metolachlor EPOST. Cotton lint yield was increased 330 to 910 kg/ha with the addition of a POST herbicide treatment compared with systems without a POST/PDS treatment. The addition of a LAYBY herbicide treatment increased cotton lint yield by 440 kg/ha compared with systems without a LAYBY.

Field studies were conducted at four locations in North Carolina in 1998 and 1999 to evaluate the use of the Herbicide Application Decision Support System (HADSS™) for weed management in nontransgenic, bromoxynil-resistant, and glyphosate-resistant cotton. Weed management systems included trifluralin preplant incorporated (PPI) plus fluometuron preemergence (PRE) or no soil-applied herbicides. Postemergence (POST) options included bromoxynil, glyphosate, or pyrithiobac early POST (EPOST) followed by (fb) MSMA plus prometryn late postemergence–directed (LAYBY) or herbicide recommendations given by HADSS. Glyphosate-resistant systems provided control equivalent to or better than control provided by bromoxynil-resistant and nontransgenic systems for smooth pigweed, Palmer amaranth, large crabgrass, goosegrass, ivyleaf morningglory, and fall panicum. Trifluralin PPI fb fluometuron PRE fb HADSS POST provided equivalent or higher levels of weed control and yield than trifluralin PPI fb fluometuron PRE fb bromoxynil, glyphosate, or pyrithiobac EPOST fb MSMA plus prometryn LAYBY. The trifluralin PPI fb fluometuron PRE fb HADSS POST systems controlled large crabgrass at Goldsboro and fall panicum better than HADSS POST-only systems in nontransgenic cotton. Cotton yield and net returns in the glyphosate-resistant systems were always equal to or higher than the nontransgenic and bromoxynil-resistant systems. Net returns were higher for the soil-applied fb HADSS POST treatments in 8 of 12 comparisons with HADSS POST systems without soil-applied herbicides. Early-season weed interference reduced cotton lint yields and net returns in POST-only systems.

Four field studies were conducted in 2004 to evaluate corn tolerance, weed control, grain yield, and net returns in glufosinate-resistant (GUR), glyphosate-resistant (GYR), imidazolinone-tolerant (IT), and nontransgenic (NT) corn with various herbicide systems. No significant differences between hybrid systems were observed for weed control. Limited corn injury (< 5%) was observed for all herbicide treatments. A single early POST (EPOST) system without S-metolachlor and sequential POST over the top (POT) herbicide systems, averaged over corn hybrids and PRE and late POST-directed (LAYBY) herbicide options, provide 93 and 99% control of goosegrass, respectively, and at least 83 and 97% control of Texas panicum, respectively. A single EPOST system without S-metolachlor, averaged over corn hybrids and LAYBY treatment options, provided at least 88% control of large crabgrass. When averaged over corn hybrid and PRE herbicide options, a sequential POT herbicide system alone provided at least 98, 99, 98, and 100 control of large crabgrass, morningglory species, Palmer amaranth, and common lambsquarters, respectively. The addition of ametryn at LAYBY to a single EPOST system without S-metolachlor was beneficial for improving control of morningglory species, common lambsquarters, and Palmer amaranth, depending on location. However, the observed increases (7 percentage points or less) are likely of limited biological significance. Grain yield was variable between hybrids and locations because of environmental differences. Consequently, net returns for each hybrid system within a location were also variable. Any POT system with or without ametryn at LAYBY, averaged over corn hybrid and PRE herbicide options, provided at least 101, 97, 92, and 92% yield protection at Clayton, Kinston, Lewiston, and Rocky Mount, NC, respectively. Net returns were maximized with treatments that provided excellent weed control with minimal inputs.

Field trials were conducted in the spring of 2004 and the spring and summer of 2005 to evaluate cantaloupe tolerance to rimsulfuron and halosulfuron applied to cantaloupe at the two-leaf stage, five- to six-leaf stage, plants having 30- to 40-cm vines, and plants having up to 5-cm-diam melons. Additionally, control of eight weed species was evaluated in these trials in 2005. Cantaloupe plant injury from rimsulfuron differed among application timings and trials, but applications were generally more injurious when applied at the two early crop stages. Halosulfuron was less injurious to cantaloupe, but 31 and 14% injury occurred following the two-leaf and five- to six-leaf applications, respectively, in the second trial in 2005. In the first trial of 2005, number of marketable melons the first week of harvest was lower for all halosulfuron applications compared with the nontreated control (30 to 37% reduction). In the second trial of 2005, total number of marketable melons was comparable to the nontreated control for each of the halosulfuron treatments, except the five- to six-leaf and up to 5-cm-diam melon applications. Injury estimates were poor indicators of occurrence or absence of delays in crop earliness or number of marketable melons. Rimsulfuron was generally effective (≥ 80% control) in controlling seedling Texas panicum, large crabgrass, tall morningglory, pitted morningglory, and Palmer amaranth, but was ineffective against yellow and purple nutsedge and goosegrass. Halosulfuron was effective in controlling yellow and purple nutsedge, but was ineffective against Texas panicum, large crabgrass, goosegrass, pitted morningglory, tall morningglory, and Palmer amaranth.

Applications of metribuzin plus MSMA have been used to control goosegrass in bermudagrass turf for over 20 yr. In 2003, two goosegrass biotypes on the island of Kauai, Hawaii were found to be resistant to applications of metribuzin plus MSMA. Metribuzin plus MSMA applied at rates of 0.28 kg ai/ha plus 2.2 kg/ha, respectively, followed by MSMA at 2.2 kg/ha 7 d later, provided 100% control of two susceptible goosegrass biotypes, but no control of two resistant biotypes. At the flowering growth stage, metribuzin applied at a rate of 0.28 kg/ha controlled both susceptible biotypes (> 92%), but did not control the two resistant biotypes. Two applications of MSMA applied at a rate of 2.2 kg/ha (7 d apart) did not control any of the four biotypes at the flowering growth stage. The two resistant biotypes were approximately 100 to 200 times less sensitive to increasing rates of metribuzin than the two susceptible biotypes. The two biotypes that were resistant to metribuzin plus MSMA were also resistant to applications of simazine plus MSMA. However, all four biotypes were susceptible to applications of glyphosate and foramsulfuron.

Research was conducted for 2 yr at Marianna, AR, to determine whether the fall-planted cover crops rye, wheat, turnip, and a blend of brown and white mustard (Caliente) would aid weed management programs in conservation-tilled, enhanced, glyphosate-resistant cotton. Wheat and rye easily were established both years and turnip and mustard blend stands were better in the second year. The cover crops alone were more suppressive of Palmer amaranth, pitted morningglory, and goosegrass in 2007 than in 2008. Rye was generally superior to wheat in suppressing the three evaluated weeds. Once herbicides were applied, there were seldom differences among cover crops for a particular herbicide program as a result of the highly efficacious herbicide programs. Cotton yields were not affected by wheat, rye, or the mustard blend, but yields were lowest in plots that followed turnip both years, possibly because of allelopathy. Integration of cover crops, especially cereals, into conservation-tilled, glyphosate-resistant cotton aided early-season weed management and could reduce the selection of glyphosate for herbicide resistance.

Twenty-one grass weeds have evolved resistance to herbicides in Latin America, particularly in rice, soybean, wheat, and orchards. Junglerice, the most widespread and economically important rice weed, evolved resistance to propanil, acetyl-coenzyme A carboxylase (ACCase)-inhibitor herbicides, quinclorac, and imazapyr in Central America, Colombia, and Venezuela. Some junglerice populations are resistant to at least three herbicide modes of action. Other herbicide-resistant (HR) rice weeds are barnyardgrass and gulf cockspur to quinclorac in Brazil, and saramollagrass to ACCase-inhibitor herbicides in Colombia and bispyribac in Venezuela. Populations of weedy rice resistant to imidazolinones are now emerging, most likely originated from gene flow from imidazolinone-resistant rice. Saramollagrass also became resistant to nicosulfuron in corn in Venezuela. Eight species associated with soybean are resistant to ACCase-inhibitor herbicides in Brazil (alexandergrass, goosegrass, and southern crabgrass) and Bolivia (Louisiana cupgrass, itchgrass, sudangrass, and two common wild sorghum species). Four more ACCase-inhibitor–resistant species (hedgehog dogtailgrass, wild oat, rigid ryegrass, and Italian ryegrass) are found in Chile infesting canola and wheat. ACCase-inhibitor–resistant hood canarygrass, littleseed canarygrass, and wild oat are important in wheat in Mexico. Resistance to acetolactate synthase (ALS)-inhibitor herbicides has been reported in itchgrass, goosegrass, and Mexican grass. Italian ryegrass populations resistant to glyphosate have been found in Chile and Brazil. Glyphosate resistance has also evolved in goosegrass in Bolivia and johnsongrass in Argentina. In general, little is done to prevent resistance evolution. An exception is the stewardship programs aiming to prevent gene flow from imidazolinone-resistant rice to weedy rice. Once resistance evolves, HR populations are mostly managed by shifting to herbicides with different modes of action and, in some cases, by slightly modifying agronomic practices. Propanil formulations containing a synergist are used to manage propanil-resistant junglerice. Increased no-till agriculture and planting of glyphosate-resistant crops are likely to select more glyphosate-resistant weeds.

Laboratory and greenhouse experiments were conducted to determine the allelopathic potential of centipedegrass. Germination and growth of indicator species were evaluated in soil leachates, leaf debris, and aqueous leaf extracts of centipedegrass. Centipedegrass soil leachates did not inhibit annual bluegrass, goosegrass, henbit, large crabgrass, or perennial ryegrass germination compared with the nonfertilized control. Incorporated centipedegrass leaf debris did not reduce lettuce germination, shoot weight, or root weight compared with the control. However, shoot and root dry weights of radish were reduced with increasing rates of centipedegrass leaf debris. Six and 9 mg debris g−1 soil reduced radish shoot weight by 49 and 64%, respectively, compared with the control. Aqueous leaf extracts of centipedegrass reduced lettuce germination; however, radicle and hypocotyl length were similar to the control. These data do not conclusively suggest centipedegrass has widespread allelopathic activity; however, significant reductions in shoot and root weight of radish with increasing centipedegrass leaf debris demonstrate a pattern of inhibition of one species against another, which fulfills a requirement of allelopathic interactions.

Goosegrass is considered one of the most important grassy weeds of rice, particularly in rain-fed environments. Experiments were conducted in laboratory, screenhouse, and field to study the germination ecology of goosegrass seeds. In the laboratory, germination was greater at higher alternating temperatures (30/20 and 35/25 C) than at the lowest alternating temperatures (25/15 C). An after-ripening period of at least 3 mo was required to improve the germination of goosegrass. Germination was tolerant of salt stress but sensitive to a high degree of water stress. A pH range of 5 to 10 did not influence seed germination (92 to 95%). In the screenhouse study, seedling emergence of goosegrass was greatest (82%) for seeds placed on the soil surface, but decreased exponentially after that, no seedlings emerged at a burial depth of 8 cm. Seedling emergence and seedling dry matter declined markedly with the addition of crop residue to the soil surface at rates equivalent to 4 to 6 ton (t) ha−1. In the field, seedling emergence of goosegrass was greater under zero-till (ZT; 16 to 18%) than under minimum tillage (MINT; 8 to 11%). Because seedling emergence was greater from surface-sown seeds and emergence was favored by ZT, this species is likely to become a problematic weed in ZT systems. The information gained from this study could be used in developing effective weed management strategies.

Field studies were conducted in 1999, 2000, and 2001 to evaluate weed control and cotton response from PRE herbicides followed by (fb) trifloxysulfuron POST. In the first study, trifloxysulfuron at 3.8, 7.5, or 15 gai/ha was applied POST with or without pendimethalin at 690 gai/ha applied PRE in a factorial treatment arrangement. Visible crop injury occurred after all trifloxysulfuron applications, but injury was not affected by application of pendimethalin PRE. Cotton injury was 19 to 22% 7 d after POST treatment (DAT) from trifloxysulfuron at 3.8 to 15 g/ha but was 5 to 12% 28 DAT. Trifloxysulfuron controlled smooth pigweed, common ragweed, and common cocklebur, but spurred anoda, large crabgrass, goosegrass, and stinkgrass were not controlled by trifloxysulfuron. Morningglory species (tall morningglory, ivyleaf morningglory, and pitted morningglory) control with trifloxysulfuron at 7.5 and 15 g/ha was at least 79%, whereas velvetleaf was controlled 66% over all years. In a second study, clomazone, pendimethalin, pendimethalin plus fluometuron, pyrithiobac, or flumioxazin were applied PRE fb 7.5 g/ha trifloxysulfuron POST. Cotton injury from PRE herbicides fb trifloxysulfuron was 13 to 39% 7 DAT. Spurred anoda control exceeded 54% only with treatments that included flumioxazin or pyrithiobac PRE. Common lambsquarters, common cocklebur, and morningglory species were controlled at least 75% with all treatments that included trifloxysulfuron POST, whereas pendimethalin and clomazone usually controlled annual grasses. In both studies, the application of pendimethalin PRE controlled annual grass species and improved control of smooth pigweed and common lambsquarters over that controlled by trifloxysulfuron POST without a PRE herbicide.

A study was conducted in 2004 and 2005 to evaluate the benefit of applying fluometuron PRE versus glyphosate-only POST programs in second-generation GR cotton (Roundup Ready Flex®). Fluometuron was either included or excluded with POST application timings of glyphosate at the following cotton growth stages: (1) 3 leaf (lf) followed by (fb) 7 lf fb 14 lf (over the top) OT (2) 3 fb 7 lf OT (3) 7 lf OT fb 14 lf postemergence directed (PD), and (4) 7 fb 14 lf OT. Control of goosegrass, Palmer amaranth, pitted morningglory, sicklepod, and smellmelon was increased 2 to 8 percentage points with the addition of fluometuron PRE. The inclusion of fluometuron PRE did not improve control of barnyardgrass, browntop millet, hemp sesbania, johnsongrass, or redroot pigweed and control ranged from 81% to 84%, 69% to 75%, 94% to 94%, 87% to 89%, and 92% to 93%, respectively. By 56 d after the last POST application, control of johnsongrass, Palmer amaranth, pitted morningglory, and smellmelon was at least 83%, 93%, 92%, and 86%, respectively, with only slight differences noted among POST glyphosate programs. Control of barnyardgrass, browntop millet, and redroot pigweed was 68%, 47%, 86%, respectively, with the POST glyphosate program of 3 fb 7 lf OT, which was significantly less than all other glyphosate POST programs. Cotton yield increased 32% and 36% with the addition of fluometuron PRE to glyphosate POST programs consisting of 7 lf OT fb 14 lf PD and 7 lf fb 14 lf OT, respectively. Cotton yield for other glyphosate POST programs including an earlier 3 lf application was not improved when fluometuron was applied PRE. Without inclusion of fluometuron PRE, yield was maximized with the glyphosate POST program that included three applications of glyphosate (2,510 kg/ha). Overall, this research emphasizes the fact that weed control is important in the early season as well as in the late season in second-generation GR cotton.

Crop residues acting as mulches can influence weed seedling emergence and weed biomass. A field study was conducted to evaluate the effect of rice residue amounts (0, 3, and 6 t ha−1) on seedling emergence of eight weed species in zero-till dry-seeded rice. The highest seedling emergence of spiny amaranth, southern crabgrass, crowfootgrass, junglerice, eclipta, goosegrass, and Chinese sprangletop was observed in the absence of residue. Seedling emergence of these weeds declined with increasing residue amounts; however, the greatest and most substantial reductions in emergence occurred with 6 t ha−1 of residue. The presence of residue also resulted in less weed biomass than with the no-residue treatment. The emergence and biomass of threelobe morningglory seedlings, however, were not influenced by residue amounts. The use of residue also increased the time taken to reach 50% of maximum emergence for some species, for example, spiny amaranth and Chinese sprangletop. The results of our study suggest that the use of residue at high rates can help suppress seedling emergence and growth of many weeds. However, there is a need to integrate other weed management strategies with residue retention to achieve season-long weed control.

Cotton gins in Arkansas, western Tennessee, and western Mississippi were sampled for weed seed contamination of gin trash in fall 2007. A total of 473 samples were collected, with 453 samples from Arkansas. The objectives of this research were to determine the weed species most frequently found in gin trash and determine what means gin operators are using to dispose of gin trash. There were 25 weed species found in the gin trash samples—11 grass and 14 broadleaf weeds. Grass and broadleaf weeds were present in 41.4 and 8.5% of the samples, respectively. The most frequently found species were large crabgrass (19.0%), barnyardgrass (14.0%), goosegrass (12.9%), red sprangletop (8.2%) and Palmer amaranth (4.2%). Viable seeds of barnyardgrass, large crabgrass, Palmer amaranth, and prickly sida were present in the surface layer (0- to 25-cm depth) of gin trash piles after 1 yr of composting. Viable Palmer amaranth seeds were present in the surface layer of gin trash piles after 2 yr of composting, but no germinable seeds were found deeper than 25 cm following 1 yr of composting. Gin trash disposal involved application of the material to crop fields during the fall or winter months; composting followed by application of the compost as mulch or a soil amendment to gardens, flower beds, or crop fields; use as cattle feed; and coverage for landfills to reduce erosion and encourage growth of vegetation. Because of the demonstrated potential for weed seed dispersal via gin trash, including composted material, development of technologies to ensure disposal of a gin-trash product free of viable weed seed are justified.

Research was conducted at Marianna, AR, for 2 yr to determine whether hairy vetch and Austrian winter pea cover crops would aid weed management programs in conservation-tilled, enhanced glyphosate-resistant cotton. Both cover crops were easily established and produced rapid growth in early spring, with biomass production of 435 to 491 g m−2 by Austrian winter pea and 415 to 438 g m−2 by hairy vetch. The effect of cover crops on weed control was short-lived in both years, with herbicide programs being the major determinant of weed control and seed-cotton yield. Averaged over cover crops, seed-cotton yields when the initial in-crop glyphosate application was delayed to the four-node cotton stage were up to 710 kg ha−1 less than in a PRE herbicide program. In 1 of 2 yr, seed-cotton yields were greater in PRE-treated plots compared with a program where initial weed management was delayed to the one-leaf stage of cotton. As a result of rapid decay of hairy vetch and Austrian winter pea biomass following cotton planting and the lack of adequate Palmer amaranth, pitted morningglory, and goosegrass control in the absence of herbicides, it appears there may be minimal weed management benefits from the use of hairy vetch and Austrian winter pea in Midsouth cotton production.

Transgenic, herbicide-resistant cultivars and equipment to spindle-pick 38-cm rows has renewed interest in narrow-row cotton production. Field experiments were conducted at four locations in North Carolina during 2004 and 2005 to evaluate weed management systems in glufosinate-resistant cotton planted in 38- and 97-cm rows. Weeds included broadleaf signalgrass, goosegrass, fall panicum, large crabgrass, Palmer amaranth, smooth pigweed, pitted morningglory, and tall morningglory. Greater than 90% control of annual grasses and Amaranthus spp. in 2004 and Ipomoea spp. in both years was obtained in narrow-row cotton with glufosinate applied early POST (EPOST) and mid-POST (MPOST) to two- and six-leaf cotton, respectively. With good early-season control by glufosinate and rapid canopy closure, there was little benefit from pendimethalin, fluometuron, or pyrithiobac applied PRE, S-metolachlor or pyrithiobac mixed with glufosinate applied MPOST, or trifloxysulfuron applied late POST (LPOST) to 11-leaf cotton in 2004. In 2005, with larger weeds at initial application, glufosinate EPOST and MPOST did not adequately control annual grasses and Amaranthus spp. Pendimethalin PRE increased control to greater than 90% and increased yields 59 to 75%. Pendimethalin PRE followed by S-metolachlor or pyrithiobac mixed with glufosinate at MPOST was no more effective than pendimethalin alone. Without PRE herbicides, trifloxysulfuron applied LPOST increased Amaranthus but not annual grass control. Cotton row spacing had no effect on cotton yield and little effect on weed control.