Flumioxazin has recently (2010) been registered for aquatic use for control of hydrilla and other noxious invasive aquatic plant species. Due to the rapid degradation of flumioxazin, especially in high pH water, some hydrilla research trials have produced less than desirable results with rapid plant regrowth. Therefore, laboratory experiments were conducted to evaluate the influence of pH on flumioxazin's effect on photosynthesis. Flumioxazin applied at concentrations ≥ 200 µg ai L⁻¹ in high (9.0) pH water and ≥ 100 µg L⁻¹ in low (6.0) pH water required 68 to 123 h to reduce photosynthesis by 50% (ET₅₀). The effect of 400 µg L⁻¹ flumioxazin on photosynthesis of apical hydrilla tips was also compared at low (20 µmol m⁻² s⁻¹), medium (170 µmol m⁻² s⁻¹), and high (400 µmol m⁻² s⁻¹) light levels at pH 9.0. Low light–treated tips were still photosynthetic at approximately 73% of the nontreated control plants 168 h after treatment. Low light–treated hydrilla required an estimated 303 h to achieve a 50% reduction in photosynthesis, while high light plants only required 99 h. Chlorophyll content of hydrilla was reduced as flumioxazin concentration was increased from 100 to 1,600 µg L⁻¹. These data indicate that flumioxazin activity on hydrilla photosynthesis is influenced by herbicide concentration, water pH, and light intensity.

Nomenclature: Flumioxazin; hydrilla, Hydrilla verticillata (L.f.) Royle HYLLI.

Wild oat is the second-most abundant, but most economically important, weed across the Canadian Prairies of western Canada. Despite the serious economic effects of resistance to acetyl-CoA carboxylase (ACC) or acetolactate synthase (ALS) inhibitors or both in this weed throughout the Northern Great Plains of North America, little research has examined the basis for herbicide resistance. We investigated target-site and nontarget-site mechanisms conferring ACC- and ALS-inhibitor resistance in 16 wild oat populations from across western Canada (four ACC-inhibitor resistant, four ALS-inhibitor resistant, and eight ACC- and ALS-inhibitor resistant). The ACC1 mutations were found in 8 of the 12 ACC inhibitor-resistant populations. The Ile1781Leu mutation was detected in three populations, the Trp2027Cys and Asp2078Gly mutations were in two populations each, and the Trp1999Cys, Ile2041Asn, Cys2088Arg, and Gly2096Ser substitutions were in one population each. Three populations had two ACC1 mutations. Only 2 of the 12 ALS inhibitor-resistant populations had an ALS target-site mutation—Ser653Thr and Ser653Asn substitutions. This is the first global report of ALS target-site mutations in Avena spp. and four previously undocumented ACC1 mutations in wild oat. Based on these molecular analyses, seedlings of five ACC ALS inhibitor-resistant populations (one with an ACC1 mutation; four with no ACC or ALS mutations) were treated with malathion, a known cytochrome P450 monooxygenase inhibitor, followed by application of one of four ACC- or ALS-inhibiting herbicides. Malathion treatment often resulted in control or suppression of these populations, suggesting involvement of this enzyme system in contributing to resistance to both ACC and ALS inhibitors.

Nomenclature: Wild oat, Avena fatua L. AVEFA.

Giant ragweed germination is delayed by both a physiological dormancy of the embryo (embryo dormancy) and an inhibitory influence of embryo-covering structures (covering structure-enforced [CSE] dormancy). To clarify the roles of embryo and CSE dormancy in giant ragweed seedling emergence timing, we conducted two experiments to address the following objectives: (1) determine changes in germinability for giant ragweed dispersal units (hereafter “involucres”) and their components under natural burial conditions, and (2) compare embryo and CSE dormancy alleviation and emergence periodicity between successional and agricultural populations. In Experiment 1, involucres were buried in crop fields at Columbus, OH, periodically excavated, and brought to the laboratory for dissection. Involucres, achenes, and embryos were then subjected to germination assays at 20 C. In Experiment 2, temporal patterns of seedling emergence were determined at a common burial site. Reductions in embryo and CSE dormancy were compared with controlled-environment stratification followed by germination assays at 12 and 20 C, temperatures representative of soil conditions in spring and summer. Results indicated that overwinter dormancy loss involved sequential reductions in embryo and CSE dormancy. CSE dormancy, which may limit potential for fatal germination during fall, was caused by the pericarp and/or embryo-covering structures within the pericarp. In Experiment 2, successional populations emerged synchronously in early spring, whereas agricultural populations emerged throughout the growing season. Levels of embryo dormancy were greater in the agricultural populations than the successional populations, but CSE dormancy levels were similar among populations. In 12 C germination assays, embryo dormancy levels were positively correlated with time required to reach 95% cumulative emergence (run 1: r  =  0.81, P  =  0.03; run 2: r  =  0.76, P  =  0.05). These results suggest that late-season emergence in giant ragweed involves high levels of embryo dormancy that prevent germination at low temperatures in spring.

Nomenclature: Giant ragweed, Ambrosia trifida L. AMBTR.

Weed composition may vary because of natural environment, management practices, and their interactions. In this study we presented a systematic approach for analyzing the relative importance of environmental and management factors on weed composition of the most conspicuous species in sugarcane. A data-mining approach represented by k-means cluster and classification and regression trees (CART) were used for analyzing the 11 most frequent weeds recorded in sugarcane cropping systems of northern Argentina. Data of weed abundance and explanatory factors contained records from 1976 sugarcane fields over 2 consecutive years. The k-means method selected five different weed clusters. One cluster contained 44% of the data and exhibited the lowest overall weed abundance. The other four clusters were dominated by three perennial species, bermudagrass, johnsongrass, and purple nutsedge, and the annual itchgrass. The CART model was able to explain 44% of the sugarcane's weed composition variability. Four of the five clusters were represented in the terminal nodes of the final CART model. Sugarcane burning before harvesting was the first factor selected in the CART, and all nodes resulting from this split were characterized by low abundance of weeds. Regarding the predictive power of the variables, rainfall and the genotype identity were the most important predictors. These results have management implications as they indicate that the genotype identity would be a more important factor than crop age when designing sugarcane weed management. Moreover, the abiotic control of crop–weed interaction would be more related to rainfall than the environmental heterogeneity related to soil type, for example soil fertility. Although all these exploratory patterns resulting from the CART data-mining procedure should be refined, it became clear that this information may be used to develop an experimental framework to study the factors driving weed assembly.

Nomenclature: Bermudagrass, Cynodon dactylon Pers. (CYNDA); johnsongrass, Sorghum halepense (L.) Pers. (SORHA); purple nutsedge, Cyperus rotundus L. (CYPRO); itchgrass, Rottboellia exaltata (L.) L.f.(ROOEX).

Natural dissemination of johnsongrass seeds as well as the effect of combine harvesting on this process were studied in corn fields. The estimation of natural dispersal was carried out by two different methods, collecting seeds throughout the season using seed traps and sampling soil–surface seed abundance before harvest using a vacuum device. Both methods showed the same dispersal pattern. A minimum of 84.6% was dispersed in the first 2 m from the focus and a maximum of 1.6% was dispersed beyond the first 5 m. An average of 76.3% of these dispersed seeds were lost or buried after shedding but before harvest. Seed dispersal by the combine harvester was estimated from the difference between soil–surface seed abundance in the same sites pre and postharvest. Although the quantity of seeds dispersed by the combine was similar to those dispersed by natural factors, dispersal distances were significantly higher. Around 90% of the dispersed seeds were found in the first 5 m forward and backward of the combine direction from the infestation source, and 1.6% of the seeds were found beyond 22 m forward and 10 m backward of the combine direction from the infestation source. A large proportion of the seeds dispersed were dormant or not viable. It is concluded that the major role of sexual reproduction in johnsongrass population dynamics may be to spread the risks, promoting dispersal in time and space.

Nomenclature: Johnsongrass, Sorghum halepense (L.) Pers. SORHA; corn, Zea mays L.

Silverleaf nightshade is a widespread, deep-rooted, summer-growing perennial that significantly reduces production in Australian crop and pasture systems. It has an extensive root system, which competes both directly and indirectly with summer and winter pastures and crops through depletion of soil moisture and nutrients. Long-distance dispersal of seeds is an important mechanism for its spread and management. A range of experiments was conducted to determine the factors influencing seed production and seedbank dynamics. Seed production ranged from 1,814 to 2,945 m⁻². Diurnally fluctuating temperatures of 25/15 C provided the optimal thermal conditions for germination, with germination not affected by light. Osmotic stress reduced germination, with no germination occurring at −1MPa. Germination was reduced to 5% at 160 mM NaCl, suggesting some salt sensitivity. Germination occurred over a pH range of 4 to 10, but declined with increasing acidity. Viability of buried seed declined to around 20% after 3 yr, with seed buried at 10 cm remaining the most viable. The prolonged seed persistence in the soil indicates a long-term control program is necessary for depleting the soil seedbank.

Nomenclature: Silverleaf nightshade, Solanum elaeagnifolium Cav. SOLEL.

Leafy spurge seeds are responsive to alternating temperature rather than constant temperature for germination. Transcriptome changes of dry leafy spurge seeds and seeds imbibed for 1 and 3 d at 20 C constant (C) and 20 ∶ 30 C alternating (A) temperature were determined by microarray analysis to examine temperature responsiveness. Principal component analysis revealed differences in the transcriptome of imbibed seeds based on the temperature regime. Computational methods in bioinformatics parsed the data into overrepresented AraCyc pathways and gene regulation subnetworks providing biological context to temperature responses. After 1 d of imbibition, the degradation of starch and sucrose leading to anaerobic respiration were common pathways at both temperature regimes. Several overrepresented pathways unique to 1 d A were associated with generation of energy, reducing power, and carbon substrates; several of these pathways remained overrepresented and up-regulated at 3 d A. At 1 d C, pathways for the phytohormones jasmonic acid and brassinosteroids were uniquely overrepresented. There was little similarity in overrepresented pathways at 1 d C between leafy spurge and arabidopsis seeds, indicating species-specific effects upon imbibition of dry seeds. Overrepresented gene subnetworks at 1 d and 3 d at both temperature regimes related to signaling processes and stress responses. A major overrepresented subnetwork unique to 1 d C related to photomorphogenesis via the E3 ubiquitin ligase COP1. At 1 d A, major overrepresented subnetworks involved circadian rhythm via LHY and TOC1 proteins and expression of stress-related genes such as DREB1A, which is subject to circadian regulation. Collectively, substantial differences were observed in the transcriptome of leafy spurge seeds imbibed under conditions that affect the capacity to germinate.

Nomenclature: Mouse-ear cress, Arabidopsis thaliana (L.) Heynh.; leafy spurge, Euphorbia esula L. (EPHES).

The dynamics of the host–parasite relationship between tomato cv. Brigade and Egyptian broomrape is temperature-related. This relationship was utilized for the development of an equation on the basis of thermal time (as measured by growing degree days, GDD, C) to predict the parasitism dynamics of Egyptian broomrape in tomato. To obtain a reliable prediction from thermal time values, studies based on a wide range of temperatures are essential. Four temperature-regime treatments and five levels of infestation with Egyptian broomrape seeds were tested in a multiclimate greenhouse (phytotron) and a temperature-controlled greenhouse, respectively. The day/night temperature regimes were 20/12 C, 23/15 C, 26/18 C, and 29/21 C and the infestation levels were 0 (noninfested control), 1, 5, 10, and 25 mg of Egyptian broomrape seeds per liter of soil. As expected, increasing temperature or infestation levels resulted in faster appearance and higher rate of attachments, respectively. The relation between development of attachments and GDD was described as a three-parameter logistic curve. In both temperature-regime and infestation-level experiments, the development of attachments began 200 GDD after planting and the maximal number of attachments was recorded 800 GDD after planting. A significant reduction in the aboveground biomass of the tomato plants due to increased Egyptian broomrape biomass was recorded only for the 26/18 C and 29/21 C day/night treatments and the three highest infestation levels (5, 10, and 25 mg L⁻¹ soil). The ability to predict the start of parasitism can be used to develop a climate-based system for Egyptian broomrape control with herbicides.

Nomenclature: Egyptian broomrape; Phelipanche aegyptiaca Pers. (syn. Orobanche aegyptiaca); tomato; Lycopersicon esculentum L.

Tall morningglory is an annual broadleaf vine and a problem weed in many annual and perennial crops in several countries including the United States. A better understanding of the germination biology of tall morningglory would facilitate the development of better control strategies for this weed. Experiments were conducted under greenhouse and laboratory conditions to evaluate the effects of various environmental factors, such as temperature, light, planting depth, pH, osmotic and salt stress, and flooding duration, on the germination of tall morningglory. The results suggested that the optimum day/night temperature range for the germination of tall morningglory was 20/12.5 to 35/25 C and maximum germination (89%) was observed at 30/20 C. Temperature higher and lower than the optimum range significantly reduced germination. Alternate light and dark did not have any adverse effect on the germination of tall morningglory seeds. The germination was 10% at an osmotic stress of −0.3 and −0.4 MPa, and above that, no germination was observed. Tall morningglory showed some tolerance to salt stress. The germination was 40% and 12% at salt concentrations of 50 mM and 200 mM, respectively. Germination was affected by pH levels, and maximum germination occurred at pH 6, whereas above or below that level, germination was significantly reduced. Maximum germination of seeds was 83 and 94% when sown at 0 and 2 cm depth in soil, within a week of sowing; however, germination was significantly reduced to 76% when placed at a depth of 4 cm or deeper. Under no flooding treatment, 87% of seed germinated, but flooding delayed and inhibited the germination of tall morningglory seeds. It is concluded that several environmental factors affected the germination of tall morningglory, and this information could help to predict the spread of tall morningglory in new areas such as Florida.

Nomenclature: Tall morningglory, Ipomoea purpurea (L.) Roth, PHBPU.

Modification of the cropping environment to make weed seed more susceptible to fatal germination or decay processes is based, in part, on the premise that seed longevity is affected by the crop-influenced environment in which seed is produced, hereafter, called the maternal crop environment. The objective of this investigation was to determine the influence of maternal crop environment on wild-proso millet seed production, germinability, and seed coat tone (i.e., lightness), a trait previously associated with seed longevity in wild-proso millet. Maternal corn environments were established by growing wild-proso millet plants in four morphologically different sweet corn hybrids in four replicates over 2 yr. Wild-proso millet seed was collected at sweet corn harvest, enumerated, characterized for seed coat tone, and tested for germination. Principal component factor analysis reduced six sweet corn traits measured between silking and harvest into a single maternal corn environment factor that accounted for 84% of the variation among crop canopies. Functional relationships between maternal corn environment factor scores and wild-proso millet seed characteristics were clarified by fitting linear models. For each unit decrease in maternal environment factor score, wild-proso millet seed production increased 1,535 seed m⁻², germination increased 2.2%, and seed coat tone was 1.8% lighter. These results show the size and germinability of wild-proso millet seed was highest in less-competitive maternal corn environments characterized by a short time to crop maturity and a small crop-canopy size.

Nomenclature: Wild-proso millet, Panicum miliaceum L., PANMI; sweet corn, Zea mays L.

A perennial species in its native range of Asia and Africa, Benghal dayflower in North America establishes annually from seed. This species has the unique ability to produce aerial and subterranean flowers and seeds. Information on how various environmental factors affect Benghal dayflower aerial and subterranean seed germination and emergence in the United States is lacking. Studies were conducted to determine the effect of temperature, planting depth, salt concentration, and pre-emergence herbicides on germination or emergence of aerial and subterranean Benghal dayflower seed. Maximum aerial seed germination occurred at 30 C, whereas maximum subterranean seed germination occurred at 30 and 35 C. Germination at 40 C was delayed relative to optimum temperatures. The seed coats in this study were mechanically disrupted to evaluate the response of seeds to temperature in the absence of physical dormancy. The physical dormancy imposed by the seed coat could require additional study. Benghal dayflower was not tolerant to ≥ 10 mM NaCl, indicating that this exotic species is not likely to become problematic in brackish marshes and wetlands of coastal plain regions. There was an inverse linear response of Benghal dayflower emergence and planting depth, with no emergence occurring at a planting depth of 12 cm. A field survey of Benghal dayflower emergence revealed that 42% of plants established from a depth of 1 cm in the soil profile, with 7 cm being the maximum depth from which seedlings plants could emerge. This suggests that PRE herbicides must remain in the relatively shallow depths of the soil profile to maximize control of germinating seedlings. Subterranean seeds were less sensitive than aerial seeds to S-metolachlor, the primary means of controlling this species in cotton. There were no differences between the germination of aerial and subterranean seed in response to treatment with diclosulam.

Nomenclature: Diclosulam; S-metolachlor; Benghal dayflower, Commelina benghalensis L., COMBE; cotton, Gossypium hirsutum L.; peanut, Arachis hypogaea L.

The critical period of weed control (CPWC) for ‘Pardina’ and ‘Brewer’ lentil was determined in field experiments near Pullman, WA, in 2008 and 2009. Trial treatments were kept either weed free for periods of 0, 14, 25, 35, 45, 60, 75, or ∼90 d after emergence (DAE), or weeds were allowed to grow before removal for periods of 0, 14, 25, 35, 45, 60, 75, or ∼90 DAE. Averaged across varieties, lentil with season-long weed interference had 29.5 and 32% seed yield reduction compared to weed-free lentils in 2008 and 2009, respectively. When measured at crop maturity, a 1% loss in lentil seed yield resulted from each 5.68 g m⁻² of dry weed biomass. Based on a 5% yield loss threshold, the CPWC for lentil was estimated to be from 270 to 999 growing degree days (GDD), 22 to 57 DAE, or crop growth stage (CGS) 7 to the early pod stage during 2008. In 2009, the CPWC was 624 to 650 GDD, with no occurrence of a CPWC when estimated using DAE and CGS. Spiny sowthistle emerged and competed with the lentil crop later in the growing season than mayweed chamomile, indicating that mayweed chamomile may be an earlier and stronger competitor than spiny sowthistle.

Nomenclature: Mayweed chamomile, Anthemis cotula L.; prickly lettuce, Lactuca serriola L.; spiny sowthistle, Sonchus asper (L.) Hill; lentil, Lens culinaris Medik. ‘Pardina’ and ‘Brewer’.

The critical period for weed control (CPWC) is an integral component of integrated weed management strategies. Several studies have defined the CPWC in soybean under varying agronomic conditions, yet none have described the mechanisms involved in crop yield losses caused by weed competition. We hypothesized that under nonresource-limiting conditions, morphological changes resulting from the expression of shade avoidance could be used to define a period of developmental sensitivity to low red-to-far-red ratio (R ∶ FR) that would overlap with the defined CPWC in soybean. Two experiments (a sequential harvest and a weed addition/removal series) were conducted in 2008 and 2009 under controlled environmental conditions to address this hypothesis. Two light-quality treatments were used: (1) high R ∶ FR ratio (i.e., weed-free), and (2) low R ∶ FR ratio (i.e., weedy). The low R ∶ FR ratio treatment induced shade avoidance responses in soybean, which included increases in height, internode length, and the shoot ∶ root ratio, as well as a reduction in biomass accumulation and leaf number. Using the morphological changes in biomass and leaf number observed in the weed addition/removal series, a period of developmental sensitivity to low R ∶ FR was defined between the first trifoliate (V1) and third trifoliate (V3) stages of soybean development. This period was found to be very similar to the CPWC previously defined by field studies of soybean–weed competition.

Nomenclature: Soybean, Glycine max (L.) Merr.

Weeds can infest management-intensive grazed pastures and impact forage quantity, forage quality, and animal health. Common burdock, plumeless thistle, and Canada thistle are three common pasture weeds in the midwestern United States that are managed to avoid these impacts. Experiments were established at two sites to determine if increasing grazing heights from fall through summer would reduce emergence and survival of burdock, plumeless thistle, and Canada thistle seedlings. Five simulated grazing heights (5, 10, 15, and 20 cm and a not-clipped treatment) were implemented in October 2008 and repeated in May through August. Density of all species was reduced from May to September, with reductions ranging from 65 to 78%, regardless of treatment. Treatments that left at least 15 cm of residual grass had reduced densities of burdock and Canada thistle compared to the 10-cm treatment. Regression analysis demonstrated that reduction in burdock and summed planted weed density was related to increased intercepted photosynthetically active radiation from forage in April. However, total biomass yield was reduced up to 60% when grazing heights were increased from 5 to 20 cm, although differences were only observed at the fall and early spring grazing events. Relative forage quality (RFQ) was similar across treatments, except at the third grazing event for which the 15 and 20-cm treatments had reduced RFQ compared with other treatments. Results suggest that increasing grazing heights can reduce emergence and survival of burdock and Canada thistle but can also result in a reduction in forage quantity in the fall and early spring.

Nomenclature: Canada thistle, Cirsium arvense (L.) Scop.; common burdock, Arctium minus Bernh.; plumeless thistle, Carduus acanthoides L.

Glyphosate is regularly used to control annual bluegrass populations in dormant bermudagrass turf. A population of annual bluegrass not controlled by glyphosate at 840 g ha⁻¹ (glyphosate resistant, GR) was identified on a golf course in Humboldt, TN in 2010. Mature tillers of GR plants were established in a greenhouse and treated with glyphosate at 0, 210, 420, 840, 1,680, 3,360, and 6,720 g ha⁻¹. Mature tillers of a biotype known to be susceptible to glyphosate (SS) were also established in the greenhouse and subjected to the same treatments. At 14 d after treatment (DAT), glyphosate controlled the SS biotype > 95% at rates > 420 g ha⁻¹. Comparatively, the GR biotype was only controlled 76% with glyphosate at 6,720 g ha⁻¹. The rates required to provide 50% control (I₅₀ values) for SS and GR biotypes were 236 and 2,812 g ha⁻¹ respectively, resulting in a resistance factor of 12. Photochemical efficiency (F_v/F_m) values on SS plants treated with glyphosate at > 210 g ha⁻¹ measured 0.000 at 14 DAT, whereas F_v/F_m values on GR plants were not significantly different from the untreated control with glyphosate rates ≤ 840 g ha⁻¹ on the same date. In laboratory experiments, the SS biotype accumulated greater shikimate concentrations than the GR biotype 3 to 6 DAT. Future research should evaluate strategies for managing GR and SS annual bluegrass with alternative modes of action.

Nomenclature: Annual bluegrass, Poa annua L.; bermudagrass, Cynodon dactylon L. Pers.; glyphosate; photochemical efficiency.

A wild population of a plant species, especially a cross-pollinated species, can display considerable genetic variation. Genetic variability is evident in differential susceptibility to an herbicide because the population can show continuous phenotypic variation. Recent, recurrent selection studies have revealed that phenotypic variation in response to low herbicide rates is heritable and can result in rapid evolution of herbicide resistance in genetically variable cross-pollinated rigid ryegrass. In this study, the heritable genetic variation in an herbicide-susceptible rigid ryegrass population was exploited to shift the population toward greater herbicide susceptibility by recurrent selection. To enhance herbicide susceptibility, herbicide-susceptible rigid ryegrass plants were divided into two identical clones, and one series of cloned plants was treated with a low rate of herbicide (diclofop). The nontreated clones of individuals that did not survive the herbicide treatment were selected and bulk-crossed to obtain the susceptible progeny. After two cycles of selection, the overall susceptibility to diclofop was doubled. The results indicate that minor genes for resistance are present in an herbicide-susceptible rigid ryegrass population, and their exclusion can increase susceptibility to diclofop.

Nomenclature: Diclofop; rigid ryegrass, Lolium rigidum Gaudin. LOLRI.

Field studies were used to examine the management strategies of mowing, herbicide, fertility, and all possible combinations on tall ironweed populations, weed biomass, and pasture yield at three Kentucky locations. Mowing was performed in July 2008 and 2009, herbicide was applied in August 2008, and fertilizer was applied in September 2008 and 2009 at all locations. Weed populations were measured in 2008, 2009, and 2010, and forage grass, clover, and weed biomass was collected in May or early June of 2009 and 2010. All treatments with herbicide reduced tall ironweed stems by 64% or greater in 2009 at all locations. Mowing alone, fertilizer alone, and mowing plus fertilizer did not reduce tall ironweed populations, except at one location where mowing alone reduced tall ironweed stems by 64% in 2009. Tall ironweed stems were not reduced in 2010 with any treatment at two locations, but herbicide combined with mowing or fertilizer reduced tall ironweed stems by 78% at the other location. Tall goldenrod population was reduced up to 100% by all treatments with herbicide or mowing alone, and mowing with fertilizer reduced tall goldenrod from 59 to 89%. Treatments did not reduce horsenettle populations. Herbicide-containing treatments reduced weed biomass at all locations. Weed biomass did not differ when comparing all treatments with and without mowing or treatments with or without fertilizer. Forage grass biomass was greatest with herbicide plus fertilizer and with the combination of mowing plus herbicide plus fertilizer at all locations in both years.

Nomenclature: horsenettle, Solanum carolinense L. SOLCA; tall goldenrod, Solidago canadensis L. var. scabra Torr. & Gray SOOAL; tall ironweed, Vernonia altissima Nutt. VENAL; tall fescue, Lolium arundinaceum (Schreb.) S. J. Darbyshire FESAR.

Previous greenhouse studies with a noncommercial glyphosate-resistant sugarbeet variety indicated that susceptibility to Rhizoctonia crown and root rot could increase after glyphosate was applied. Greenhouse and field experiments were conducted in 2008 and 2009 to determine if glyphosate influenced disease severity in potential commercially available varieties of glyphosate-resistant sugarbeet. In the first greenhouse experiment in 2008, Hilleshög 9027RR, the most tolerant variety to Rhizoctonia crown and root rot, exhibited an increase in disease severity when glyphosate was applied. There were no significant differences between herbicide treatments in Hilleshög 9028RR, and glyphosate decreased disease severity in Hilleshög 9032RR when compared with the no-herbicide treatment. Experiments conducted to determine if glyphosate influenced Rhizoctonia solani growth in vitro indicated that glyphosate did not increase the radial growth of R. solani, except at 10× (190 µg ae ml⁻¹) the normal rate of glyphosate plus ammonium sulfate (AMS). Field and additional greenhouse experiments were conducted using four commercial varieties. Differences in disease severity were observed when comparing varieties, but glyphosate did not significantly influence the severity of Rhizoctonia crown and root rot when compared with the no-herbicide control. Choosing a glyphosate-resistant sugarbeet variety with the best demonstrated tolerance to Rhizoctonia crown and root rot is an important factor in reducing disease severity and maintaining sugarbeet yield.

Nomenclature: Glyphosate; sugarbeet, Beta vulgaris L.; Rhizoctonia crown and root rot, Rhizoctonia solani Kühn.

Rapid adoption of glyphosate-resistant (GR) corn hybrids has led to the reemergence of volunteer corn as a problematic weed in soybean and has made controlling the initial stand of corn in a replant situation more difficult. If volunteer corn in soybean or the initial corn stand in a replant situation is not controlled, yield loss can occur. Clethodim and glufosinate are often used to control GR corn in corn replant situations and in soybean. The objectives of this research were to evaluate the response of two hybrid corn varieties and their F₂ progeny to clethodim and glufosinate and to evaluate the effect of plant nitrogen (N) concentration on clethodim and glufosinate efficacy. First, a dose-response study was conducted with clethodim and glufosinate on DeKalb 60-18 and 60-18F₂, and DeKalb 63-42 and 63-42F₂ to compare the response of the hybrids and their F₂ progeny to the herbicides. DeKalb 63-42 was more tolerant to clethodim than 60-18 and 60-18F₂. No differences were found between the hybrids and their respective F₂ progeny in the response to clethodim or glufosinate. In a second dose-response study assessing the effect of N conditions on herbicide efficacy, both clethodim and glufosinate were less injurious to plants growing in low N than in high N availability.

Nomenclature: Clethodim; glufosinate; corn Zea mays L.; soybean Glycine max (L.) Merr.

The increasing use of synthetic chemicals for pest control in rice has become an overwhelming economical border, and more important, it could pose a serious threat of the environment. In addition, the extensive use of synthetic herbicides has been the cause for the evolution of herbicide-resistant barnyardgrass worldwide. This weed species is the most competitive weed in rice after the red rice. Thus, this study was conducted to examine the combination effects of aqueous sunflower leaf extracts with lower rate of pretilachlor on barnyardgrass emergence and growth in Marang (sandy loam) and Seberang (silt loamy) soil series under glasshouse conditions. Interestingly, the ED₉₅ values (rate that causes 95% inhibition) of pretilachlor for emergence and shoot fresh weight (SFW) of barnyardgrass were reduced by 79 and 82%, respectively, when being mixed with sunflower leaf extracts in Marang series. In contrast, the addition of sunflower leaf extracts increased ED₉₅ value of pretilachlor in Seberang series. Rice seedlings at 4 and 8 d after sowing (DAS) were found to be tolerant to this mixture treatment. However, root growth of rice seedlings were inhibited at 0 and 2 DAS. These results suggest that sunflower leaf extracts have potential to reduce rate of pretilachlor for inhibiting emergence and growth of barnyardgrass without injuring rice seedlings in rice fields depending on soil types and growth stage of rice.

Nomenclature: Pretilachlor, 2-chloro-N-(2,6-diethylphenyl)-N-(2-propoxyethyl)acetamide; barnyardgrass, Echinochloa crus-galli (L.) Beauv., ECHCG; rice and red rice biotype, Oryza sativa L.; sunflower, Helianthus annuus L.

In a 4-yr field study, “weed suppressive” rice cultivars provided 30% greater control of barnyardgrass and sustained 44% less yield loss (relative to weed-free) compared to “nonsuppressive” tropical japonica rice cultivars. ¹³C analysis revealed that rice root mass predominated vertically and laterally within the soil profile of plots infested with barnyardgrass. Among all cultivars, rice roots accounted for 75 to 90% of the total root mass in samples, and this was most concentrated in the surface 5 cm of soil in the row. Barnyardgrass roots were most prevalent in the surface 5 cm between rows where they accounted for 30% of total root mass. Overall, barnyardgrass root mass was about twice as high in nonsuppressive rice compared to suppressive rice. Weed suppression by indica/tropical japonica rice crosses generally was intermediate between that of the other two rice groups. At the 0- to 5-cm depth, between-rows, barnyardgrass root mass was correlated negatively with rice height (r  =  −0.424), yield (r  =  −0.306), and weed control ratings (r  =  −0.524) in weedy plots. Control ratings in weedy plots also were negatively correlated with rice percent height reduction (r  =  −0.415) and % yield loss (r  =  −0.747) relative to weed-free plots, and with barnyardgrass root mass as a percent of total root mass (r  =  −0.612). Control ratings were positively correlated with rice yield under weed pressure (r  =  0.429) but were correlated with rice root mass in-rows only (r  =  −0.322). Clearly, rice root mass could not have been the major cause of the differences in barnyardgrass control between cultivars.

Nomenclature: Barnyardgrass, Echinochloa crus-galli (L.) Beauv.; rice, Oryza sativa L.