Inhibitors of acetolactate synthase (ALS) are important herbicides for control of wild mustard, a common weed of the north central United States and Canada. Wild mustard that survived treatments with the ALS inhibitors cloransulam, imazethapyr, and thifensulfuron was sampled from a North Dakota soybean field in 1999. The mechanism of resistance and response of this wild mustard biotype to ALS-inhibiting herbicides was investigated. In vitro enzyme-inhibition experiments confirmed a resistance mechanism associated with the ALS enzyme; imazethapyr or imazamox at 1 × 10⁻⁴ M caused only 10 to 11% and 12 to 16% reductions in ALS activity, respectively. ALS from a susceptible wild mustard biotype was inhibited 50% (I₅₀) with imazethapyr at 8 × 10⁻⁷ M or imazamox at 1.1 × 10⁻⁶ M. Whole-plant greenhouse treatments confirmed cross-resistance across ALS-inhibitor classes. Treatment with twice-normal field rates of thifensulfuron, ethametsulfuron, triflusulfuron, imazamox, imazethapyr, flumetsulam, cloransulam, flucarbazone, and imazamethabenz reduced biomass of the susceptible biotype at least 96% 28 d after treatment. Biomass of the resistant biotype was reduced 49% by triflusulfuron and 35% by thifensulfuron, but was not reduced by other herbicides. DNA sequence analysis of ALS genes from resistant and susceptible biotypes revealed a point mutation inferring a Trp-to-Leu amino acid substitution in ALS of the resistant biotype. This mutation, corresponding to position 574 of the Arabidopsis ALS amino acid sequence, is known to confer cross-resistance to ALS-inhibiting herbicides and is the probable cause of resistance in the wild mustard biotype. Phylogenetic analysis of wild mustard and canola ALS sequences confirmed that the Trp₅₇₄ mutation arose within wild mustard and was not derived via introgression from imidazolinone-resistant canola. The results of this research indicate a naturally occurring target-site point mutation responsible for conferring cross-resistance to ALS-inhibiting herbicides in this wild mustard biotype.

Nomenclature: Cloransulam, ethametsulfuron, flucarbazone, flumetsulam, imazamethabenz, imazamox, imazethapyr, thifensulfuron, triflusulfuron, Arabidopsis, Arabidopsis thaliana (L.) Heynh., ARBTH; wild mustard, Sinapis arvensis L., SINAR; canola, Brassica napus L.; soybean, Glycine max (L.) Merr.

African rue is an exotic, herbaceous perennial established in several western states that tolerates harsh, water-stressed conditions. The influence of water-deficit stress on herbicide response and subsequent herbicide fate within the plant were compared. African rue seedlings were deprived of water for 0 to 7 d to establish a gradient of water-deficit levels before treatment with hexazinone, imazapyr, or metsulfuron. At herbicide application, water-deficit treatments reduced plant water potential values from −1.0 MPa to −4.7 MPa, causing concomitant reductions in photosynthesis. Thirty-five days after treatment, dry weight of imazapyr- and metsulfuron-treated plants was reduced in plants exposed to more than 4 d water-deficit stress before herbicide application. In contrast, hexazinone-treated plants had less dry weight than water-stressed, nonsprayed control plants regardless of water-deficit stress. Seventy-two hours after herbicide application, African rue leaves absorbed from 5 to 42% of herbicide applied; however, herbicide absorption did not correlate to efficacy. Less than 12% of absorbed herbicide translocated out of the treated leaf, regardless of herbicide. Radiolabel translocated from the treated leaf to acropetal or root tissue did not differ among herbicide treatments, regardless of water deficit before herbicide application. However, compared to other herbicides, translocation to basipetal shoot tissue was greatest in imazapyr-treated seedlings with the largest water deficit at herbicide application. Increased translocation occurred at higher levels of water stress than were necessary to increase herbicide efficacy, suggesting differential translocation was not involved in enhanced efficacy. In summary, African rue seedlings absorbed and mobilized three different herbicides at all levels of water-deficit stress. In addition, the efficacy of metsulfuron and imazapyr increased as water-deficit stress increased, but efficacy of hexazinone was not influenced by plant water status. This unusual relationship between water-deficit stress and herbicide performance may enable improved African rue management under stressful environments.

Nomenclature: African rue, Peganum harmala L. PEGHA.

A series of dose–response experiments were performed at low humidity to determine if glufosinate efficacy could be increased by lengthening the drying time through the addition of humectants. Of several humectants evaluated, only 5% glycerol or 5% triethylene glycol when applied with glufosinate produced dry weight reductions and mortality similar to exposure to high humidity. ¹⁴C-glufosinate movement through isolated wild oat cuticles was greater at high humidity, poorest at low humidity, but intermediate at low humidity in the presence of 5% glycerol in the spray solution. The increases in uptake observed at high humidity and with 5% glycerol at low humidity were characterized by greater initial uptake that continued much longer than that observed at low humidity without humectant.

Nomenclature: Wild oat, Avena fatua L. AVEFA.

In Australia, glyphosate resistance has been observed in rigid ryegrass in several states including New South Wales (NSW) and South Australia (SA). Several populations of glyphosate-resistant rigid ryegrass were analyzed for the inheritance of glyphosate resistance. Eight glyphosate-resistant populations were crossed to the same susceptible population to create first filial generation (F₁) families. Individuals from the F₁ families were subsequently treated with glyphosate. The response to glyphosate of F₁ families from all eight crosses was more similar to the resistant parent than the susceptible parent. Within crosses, dose responses of reciprocal F₁ families were not significantly different from each other, indicating glyphosate resistance is encoded on the nuclear genome in all eight populations. The level of dominance observed in dose–response experiments ranged from partial to total within the herbicide doses tested. F₁ individuals from five of the populations were crossed with susceptible (S) individuals to create backcross (BC) populations. Most of the families from these BC populations segregated in a manner consistent with a single gene controlling glyphosate resistance. These results indicate that resistance is inherited as a single dominant allele in four out of the five glyphosate-resistant rigid ryegrass populations. Such information is vital in the development of management strategies for glyphosate resistance in Australia.

Nomenclature: Glyphosate; rigid ryegrass, Lolium rigidum Gaud. LOLRI.

The expression of a candidate auxin-responsive gene was evaluated for use in a diagnostic assay for plant growth regulator (PGR) herbicide injury in soybean leaves. Expression of GH3, a primary auxin-responsive gene, was evaluated in response to dicamba and clopyralid at the RNA and protein levels, and proteomic analysis evaluated global expression of proteins in response to dicamba. Expression of GH3 was also analyzed in response to heat, drought, salt stress, and infection by soybean mosaic virus (SMV) and bean pod mottle virus (BPMV) to determine the specificity of GH3 expression as a diagnostic marker for PGR herbicide injury. At the RNA level, GH3 was strongly induced by dicamba and clopyralid within 8 h after application. Expression peaked 1 to 3 d after treatment (DAT) in response to 10% and 1% of a labeled dose of dicamba and clopyralid, with higher expression levels detected at higher herbicide rates. At the protein level, GH3 expression was also strongly induced at 1, 2, and 3 DAT by 10% vs. 1% of a labeled dose of dicamba and clopyralid. Heat, drought, and salt stress and infection with SMV or BPMV had no effect on GH3 expression at either the RNA or protein level. Proteomic analysis identified three proteins that were up-regulated in response to dicamba. Two were induced for less than 7 DAT, and a third was identified as a stress-response enzyme (superoxide dismutase) that is likely not specific to PGR herbicide injury. Expression of GH3 was highly induced by PGR herbicides at the RNA and protein level and was not affected by environmental stresses or viral infection, indicating that GH3 expression has excellent potential for use in a diagnostic assay for PGR herbicide injury.

Nomenclature: Clopyralid; dicamba; soybean, Glycine max L. Merr.

This research studies whether photoprotection mechanisms are able to counterbalance the short-term effect of two herbicides, acifluorfen methyl (AFM) and paraquat (PQ), that generate photo-oxidative stress in different subcellular locations. Duckweed plants grown under three light intensities (high-, medium-, and low light), and consequently expressing three levels of photoprotection, were exposed to both herbicides under the same light regime. Oxidative damage induced by AFM originated mainly from the cytosolic accumulation of protoporphyrin IX, leading to a process of plasma membrane disruption, a progressive and slow degradation of ascorbate and photosynthetic pigments, and glutathione accumulation. As most photoprotective mechanisms (antioxidants and xanthophylls-cycle-related energy dissipation) operate mainly within the chloroplast, these systems were unable to protect plants from AFM damage irrespective of the level of light acclimation. Paraquat effects developed more rapidly and to a greater extent than AFM in treated plants. Irrespective of the light intensity, the same sequence of degradation was observed: ascorbate followed by glutathione, α-tocopherol, pigments, and membrane disruption. In PQ-treated plants the generation of oxidative stress occurred mainly in the chloroplast, and cellular damage developed more slowly in highly photoprotected plants (high light); in fact, electrolyte leakage can be used as a marker for PQ tolerance. The effects of both herbicides indicate that the xanthophyll cycle is an early protective mechanism and confirms the central role of ascorbate in early photoprotection response. High levels of lipophilic and hydrophilic antioxidant contents did not lead to attenuated phytotoxicity of acifluorfen methyl and thus are not the basis to explain differential susceptibilities among duckweed plants.

Nomenclature: Acifluorfen; paraquat; duckweed, Lemna minor (L) LEMMI.

A downy brome population in a winter wheat field at Córdoba, Spain, survived use rates of chlortoluron (2.5 to 3.5 kg ai ha⁻¹) over 2 consecutive yr, where wheat monoculture and multiple annual chlortoluron applications had been carried out. The resistant (CR) biotype showed a higher ED₅₀ value (7.4 kg ai ha⁻¹; the concentration required for 50% reduction of fresh weight) than the susceptible (S) control (2.2 kg ai ha⁻¹), with a 3.4-fold increase in chlortoluron tolerance. Chlortoluron resistance in the CR downy brome biotype was not caused by altered absorption, translocation, or modification of the herbicide target site but by enhanced detoxification. The inhibition of both the recovery of photosynthetic electron transport and chlortoluron metabolism in the CR biotype due to the presence of the Cyt P450 inhibitor 1-aminobenzotriazole (ABT) indicates that herbicide metabolism catalyzed by Cyt P450 monooxygenases is related to chlortoluron resistance in CR plants. Although both biotypes degraded chlortoluron by N-dealkylation and ring-methyl hydroxylation and seem to share the same ability to form polar conjugates, degradation in the resistant biotype is more efficacious as this biotype metabolizes the parent herbicide faster and to a greater extent than its susceptible counterpart. The ability of the susceptible biotype to ring-hydroxylate chlortoluron, albeit at much slower rate, probably explains its moderate tolerance to chlortoluron observed in the growth assays and its minor photosynthetic electron transport recovery observed in fluorescence measurements.

Nomenclature: Chlortoluron; downy brome, Bromus tectorum L. BROTE.

Actinonin is a naturally occurring hydroxamic acid and a potent inhibitor of the essential cotranslational protein processing enzyme peptide deformylase. Actinonin has both pre- and post-emergence herbicidal activity, but it is rapidly metabolized by plants, thus limiting herbicidal efficacy. Studies designed to elucidate the metabolic fate of actinonin revealed that after absorption actinonin was metabolized by tobacco plants with only about 17% of the parent compound remaining 48 h after application. Subcellular fractionation revealed that a microsomal fraction was capable of metabolizing actinonin in vitro. Two actinonin metabolites were isolated by reverse-phase high-performance liquid chromatography and identified by mass spectrometric analyses. The major metabolite was derived from the hydrolysis of the hydroxamate group to its corresponding acid, and a relatively minor metabolite through reduction of the hydroxamate group to the corresponding amide. Both metabolites were functionally inactive as inhibitors of peptide deformylase. These results provide rationale for the low efficacy of actinonin as a broad-spectrum herbicide, and identify functional groups in actinonin targeted by plants during detoxification. This information may facilitate the design and synthesis of actinonin analogues with increased herbicidal efficacy.

Nomenclature: actinonin; tobacco, Nicotiana tabacum L. ‘Samsun NN’.

Field experiments were established in fall 1999 and 2000 near Huntley, MT, to determine the effects of soil water content on wild oat seed mortality and seedling emergence. Four supplemental irrigation treatments were implemented from June through September to establish plots with varying soil water content. Wild oat seed mortality during the summer increased linearly as soil water content increased. For seed banks established in 1999 (1999SB), seed mortality increased, on average, from 36 to 55% in 2000, and 15 to 55% in 2001 as soil water content increased from 6 to 24%. For seed banks established in 2000 (2000SB), seed mortality increased, on average, from 38 to 88% in 2001 and 53 to 79% in 2002 as soil water content increased from 6 to 24%. Increasing soil water content likely increased the activity of microorganisms that cause mortality in wild oat seeds. The increasing seed mortality rates (due to increasing soil water content) resulted in greater annual declines of wild oat seed banks and 2-yr cumulative decline rates. Total season emergence percentage was not affected by irrigation treatment. Results show that weed seed bank decline is more rapid in moist than in dry soils and suggest that management practices that increase or conserve soil moisture will also increase the rate of wild oat seed bank decline.

Nomenclature: Wild oat, Avena fatua L., AVEFA.

Knowledge about how the type, timing, and arrangement of cultural practices influence weed species composition is important for understanding the ecological results of control strategies and designing alternative crop management systems. We evaluated weed seed density, diversity, and community composition from 1997 to 1999 in a 35-yr-old study comparing cropping sequences (continuous corn, corn–soybean, corn–oat–hay) and tillage systems (conventional, minimum, and no-tillage) in Wooster, OH. Weed seedbank diversity, as measured by species richness (S), evenness (J), and the Shannon–Weiner index (H′), was influenced by crop diversity; mean values for each of the indices were generally higher for all combinations of the three-crop sequence than for the corn monoculture or the corn–soybean rotation. Except for 1998, mean seed density (to a depth of 10 cm) was higher in continuous corn (x̄ = 5,220 m⁻²) than in corn and soybean rotations (x̄ = 2,360 m⁻²). Species richness and seed density were also affected by tillage. Mean values for S (x̄ = 10.8 species) and mean germinable seeds (x̄ = 5,960 m⁻²) were greatest in the no-tillage system, where the soil was disturbed only by the coulter units of the planter. Differences in weed seedbank community composition among tillage and rotation treatments were examined using two multivariate analyses. Using a multiresponse permutation procedure and canonical discriminant analysis, results suggest that the weed seed community in a corn–oat–hay rotational system differs in structure and composition from communities associated with continuous corn and corn–soybean systems. Additionally, germinable weed seed communities in no-tillage differed in composition from those in conventional and minimum tillage. Crop sequence and tillage system influenced weed species density and diversity and therefore community structure. Manipulation of these factors could help reduce the negative impact of weeds on crop production.

Nomenclature: Oat, Avena sativa L.; soybean Glycine max L. Merr.; alfalfa, Medicago sativa L.; corn, Zea mays L.

Field and greenhouse studies were conducted in 2002 and 2003 to evaluate mechanically stimulated compensatory growth response of ivyleaf morningglory, common waterhemp, and giant ragweed. Compensatory growth was initiated by the physical removal of the apical shoot to break apical dominance. The amount of apical shoot removed had an effect on mechanically stimulated compensatory growth of common waterhemp and giant ragweed. With these species, the more of the apical shoot removed from the plant, the less compensatory growth occurred. Removal of the shoot from above the cotyledons resulted in giant ragweed that were 48% shorter and weighed 41% less than control plants at 6 wk after shoot removal. However, the amount of apical shoot removed had no effect on the growth of ivyleaf morningglory compared with control plants at the completion of the study. The influence of plant height at the time of shoot removal on compensatory growth was specific to each weed species. Ivyleaf morningglory exhibited less compensatory growth when the plants were 10 cm at the time of shoot removal compared with 20-, 30-, and 40-cm-tall plants. Removal of the shoot when common waterhemp plants were 30 or 40 cm in height reduced plant weight by 23 and 21%, respectively, compared with control plants. However, no reductions in plant weight were observed when common waterhemp were 10 or 20 cm tall at the time of shoot removal. Giant ragweed subjected to shoot removal was smaller in most growth parameters than control plants, regardless of plant height at the time of shoot removal.

Nomenclature: Common waterhemp, Amaranthus rudis Sauer AMATA; giant ragweed, Ambrosia trifida L. AMBTR; ivyleaf morningglory, Ipomoea hederacea (L.) Jacq. IPOHE.

Invasions of many different plants have occurred in ecosystems around the world and theories of the mechanisms of these invasions abound. All the proposed theories have value, and many of the proposed mechanisms may at least serve as facilitating factors, but no overarching conceptual framework for the mechanisms of plant invasion has emerged. One common theme in all invasions is that the invading plant, in the process of geographic displacement, has been dislocated from its coevolved biota and relocated with a less-familiar biota. The impacts of dislocation from coevolved mutualists, parasites, and competitors are different but follow general principles. The impacts of relocation with new mutualists, parasites, and competitors are also variable and will change as the introduced plant coevolves with its new biotic environment. I propose some hypotheses to guide predictions of the outcomes of the dislocation of plants from coevolved relationships and, hence, the outcomes of plant geographic displacement. Invasiveness in plants is not determined by their life history traits or the nature of the ecosystem they are invading. Invasiveness is primarily a result of the process of invasion itself. When plants are dislocated from coevolved relationships and confronted with new relationships, they can become ecologically transformed. This transformation can affect the ability of a plant population to become established, invasive, and naturalized in a new environment.

It has been proposed that cropping systems can be managed to promote the development of soil microbial communities that accelerate weed seed mortality. We examined soil fungal and bacterial communities, soil C:N ratio, soil particle size fractions, and weed seed mortality in soil from fields with over 10 yr of five contrasting management histories with the objective of determining if seed mortality could be explained by differences in soil properties. Seed mortality of giant foxtail and velvetleaf were greatest in soil from the conventionally managed systems and lowest in soil from a reduced input system. Principal-components analysis of soil microbial communities, as determined through denaturing gradient gel electrophoresis of polymerase chain reaction–amplified ribosomal RNA genes (PCR-DGGE), showed distinct differences in the composition of fungal and bacterial communities among the study soils. The first principal component of the 18S rDNA PCR-DGGE analysis of fungal community composition showed a strong negative correlation with both giant foxtail (− 0.52, P < 0.05) and velvetleaf (− 0.57, P < 0.01) seed mortality, as did ordination with nonmetric multidimensional scaling (NMS) [giant foxtail (− 0.54, P < 0.01) and velvetleaf (− 0.60, P < 0.01)], suggesting that seeds of the two species were affected similarly by changes in the soil fungal community. For giant foxtail, weed seed mortality was also positively correlated (r = 0.48, P < 0.05) with the first NMS axis of the bacterial 16S rDNA analysis. None of the other measured soil properties were significantly correlated with weed seed mortality. Thus, for the soils tested here, management history, microbial community composition, and weed seed mortality were linked. To extend these results to the field, more work is needed to identify components of the fungal and bacterial communities that are active in seed degradation, and to develop conservation biocontrol recommendations for these species.

Nomenclature: Giant foxtail, Setaria faberi Herrm., SETFA; velvetleaf, Abutilon theophrasti Medik., ABUTH.

Germination was investigated in 1-yr and 8-yr-old seed lots of barnyardgrass. Each seed lot was divided into a portion stored dry at 25 C (afterripening) and a portion buried in the field (stratification) in central Europe (latitude 50°N, longitude 14°E). The afterripened seed lost dormancy within 2 yr after dispersal, whereas buried seed passed through annual dormancy/nondormancy cycles. The seed was germinated at five constant temperatures between 17 and 35 C with an 18/6-h light/dark photoperiod. Germination was affected by both seed age and storage conditions. Germination percentage and rate in 8-yr-old afterripened and each of the stratified seed lots varied with temperature. Optimum temperatures for germination were between 27 and 31 C, and the range of adequate temperatures increased with seed age. A common base temperature for germination was 11.7 C. In 1-yr-old afterripened material, the proportion of germinating seed (< 5%) and germination rate were similar at all temperatures. Barnyardgrass thus revealed a plastic strategy of germination. Stratification during the first winter removed dormancy and allowed germination at a narrow range of temperatures. This constraint on optimum germination temperature decreased with increased seed age. Seedling emergence, thus, may vary according to whether seed population originates from the previous year or from old soil seed banks.

Nomenclature: Barnyardgrass, Echinochloa crus-galli (L.) Beauv. ECHCG.

Common waterhemp is an obligate outcrosser that has high genetic variability. However, under selection pressure, this weed shows population differentiation for adaptive traits. Intraspecific variation for herbicide resistance has been studied, but no studies have been conducted to determine the existence of variation for other adaptive traits that could influence weed management. The objective of this study was to examine the existence of different seed dormancy regulatory mechanisms in common waterhemp. Seed dormancy regulation, in response to different temperature and moisture regimes, was studied through germination experiments and proteome analysis using two common waterhemp biotypes (Ames and Everly) collected from agricultural fields in Iowa, and one biotype (Ohio) collected from a pristine area in Ohio. Without stratification, germination percentage among the different biotypes was 9, 29 and 88% for Ames, Everly, and Ohio respectively. The germination rate of seeds from Ames was dramatically increased after incubation at either 4 or 25 C under wet conditions, whereas germination of seeds from Everly was only increased at 25 C under wet conditions. The Ohio biotype showed no change in germination response to any of the incubation treatments. Germination studies indicated that the rate of seed dormancy alleviation differed between biotypes. Seed protein profiles obtained from the three biotypes differed in protein abundance, number, and type. A putative small heat-shock protein (sHSP) of 17.6 kDa and isoelectric point (pI) 6.1 increased whereas a putative glyceraldehyde-3-phosphate dehydrogenase (G3PDH) of 30.9 kDa and pI 6.4 decreased in abundance in the Ames biotype as seed dormancy was reduced in response to incubation at 4 C and wet conditions. These two proteins did not change in the Everly and Ohio biotypes, suggesting that these proteins changed their abundance in response to seed dormancy alleviation. The results of this study suggest that differences in seed dormancy levels between the biotypes were due to different physiological regulatory mechanisms.

Nomenclature: Common waterhemp, Amaranthus tuberculatus (Moq.) J.D. Sauer

Germination response of slender amaranth to temperature, solution pH, moisture stress, and depth of emergence was evaluated under controlled environmental conditions. Results indicated that 30 C was the optimum constant temperature for germination. Germination of slender amaranth seed at 21 d was similar, with 35/25, 35/20, 30/25, and 30/20 alternating temperature regimes. As temperatures in alternating regimes increased, time to onset of germination decreased and rate of germination increased. Slender amaranth germination was greater with acidic than with basic pH conditions. Germination declined with increasing water stress and was completely inhibited at water potentials below −0.6 MPa. Slender amaranth emergence was greatest at depths of 0.5 to 2 cm, but some seeds emerged from as deep as 6 cm. Information gained in this study will contribute to an integrated control program for slender amaranth.

Nomenclature: Slender amaranth, Amaranthus viridis L. AMAVI.

Death of the apical shoot and subsequent compensatory growth from previously inhibited axillary buds is a possible result of POST weed control practices. The objective of this research was to determine the efficacy of glyphosate and lactofen on ivyleaf morningglory, common waterhemp, and giant ragweed during mechanically stimulated compensatory growth. Plants were grown in the greenhouse to a height (or lateral growth) of 15 cm; at which time, the apical shoots were removed by cutting just above the cotyledonary node. Plants were allowed to regrow to 15 cm and treated with lactofen or glyphosate. Herbicide treatments were also applied to intact plants that were 15 cm in height for comparison. Weed response to herbicides during mechanically stimulated compensatory growth varied by weed species and herbicide. Giant ragweed under compensatory growth was less sensitive to both glyphosate and lactofen compared with intact plants. Comparison of GR₅₀ (the herbicide dose that reduced dry weight by 50%) values indicated that ivyleaf morningglory under compensatory growth was 1.5 times more sensitive to glyphosate than intact plants. Conversely, previously injured ivyleaf morningglory plants were less sensitive to lactofen than intact plants. The GR₅₀ for glyphosate applied to intact common waterhemp plants and plants under compensatory growth was similar. However, common waterhemp plants under compensatory growth were more sensitive to lactofen at the three lowest rates evaluated compared with intact plants. In summary, the efficacy of foliar herbicides applied to weeds that exhibit compensatory growth may be different from weeds under a normal growth state.

Nomenclature: Glyphosate; lactofen; common waterhemp, Amaranthus rudis Sauer AMATA; giant ragweed, Ambrosia trifida L. AMBTR; ivyleaf morningglory, Ipomoea hederacea (L.) Jacq. IPOHE.

Field studies were carried out in Laingsburg, MI, from 2002 to 2004 on Houghton muck soil to assess the impacts of cover crops and soil fertility regimes on weed populations and celery yield. The cover crops were oilseed radish, cereal rye, hairy vetch, and a bare ground control. The fertility rates were full (180, 90, and 450 kg ha⁻¹ nitrogen [N], phosphorus pentoxide [P₂O₅], and potassium oxide [K₂O], respectively), half (90, 45, and 225 kg ha⁻¹ N, P₂O₅, and K₂O, respectively), and low (90 kg ha⁻¹ N). Each cover crop treatment was combined with the low or half rate of fertilizer. An additional treatment with bare ground plus the full rate of fertilizer was added as standard practice. Treatments were maintained in the same location for the duration of the study. Major weed species were common chickweed, prostrate pigweed, shepherd's-purse, common purslane, and yellow nutsedge. Each year, oilseed radish consistently produced the greatest biomass and provided over 98% early season weed biomass suppression. Hairy vetch and cereal rye provided about 70% weed suppression in early spring. Soil fertility level affected weed populations during the 2004 growing season. In 2004, weed biomass in treatments without cover crops or with vetch increased when greater amounts of fertilizer were applied. Within individual fertility levels, higher celery yields were recorded in the oilseed radish plots. For example, in the low fertility rate, celery yield was 34.8, 29.2, 23.9, and 24.4 ton ha⁻¹ in the oilseed radish, cereal rye, hairy vetch, and control plots, respectively in 2003. Overall, the results of this experiment indicate that when included in a system where hoeing and hand-weeding are the only weed control methods, cover crops can successfully improve weed management and celery yield on muck soils, allowing reduced fertilizer inputs.

Nomenclature: Common chickweed, Stellaria media (L.) Vill. STEME; common purslane, Portulaca oleracea L. POROL; prostrate pigweed, Amaranthus blitoides S. Wats AMABL; shepherd's-purse, Capsella bursa-pastoris (L.) Medicus CAPBP; yellow nutsedge, Cyperus esculentus L. CYPES; celery, Apium graveolens L. ‘Dutchess’; cereal rye, Secale cereale L., ‘VNS’; hairy vetch, Vicia villosa Roth, ‘Common’; oilseed radish Raphanus sativus (L.) var. oleiferus Metzg (Stokes), ‘Diakon’.

Hand-held hyperspectral reflectance data were collected in the summers of 2002, 2003, and 2004 to differentiate unique spectral characteristics of common turfgrass and weed species. Turfgrass species evaluated were: bermudagrass, ‘Tifway 419’; zoysiagrass, ‘Meyer’; St. Augustinegrass, ‘Raleigh’; common centipedegrass; and creeping bentgrass, ‘Crenshaw’. Weed species evaluated were: dallisgrass, southern crabgrass, eclipta, and Virginia buttonweed. Reflectance data were collected from greenhouse and field locations. An overall classification accuracy of 85% was achieved for all species in the field. A total of 21 spectral bands between 378 and 1,000 nm that were consistent over the three data collection periods were used for analysis. Only centipedegrass, zoysiagrass, and dallisgrass were correctly classified less than 80% of the time. An overall classification accuracy of 69% was achieved for the greenhouse species. Spectral bands used in this analysis ranged from 353 to 799 nm. Creeping bentgrass and Virginia buttonweed were classified correctly at 96 and 92%, respectively.

Nomenclature: Eclipta, Eclipta prostrata L. ECLAL; Virginia buttonweed, Diodia virginiana L. DIQVI; dallisgrass, Paspalum dilatatum Poir. PASDI; southern crabgrass, Digitaria ciliaris (Retz.) Koel. DIGSP; bermudagrass, Cynodon dactylon (L.) Pers. × Cynodon transvaalensis Burtt-Davy, ‘Tifway 419’; zoysiagrass, Zoysia japonica Steud., ‘Meyer’; St. Augustinegrass, Stenotaphrum secundatum (Walt.) Kuntze, ‘Raleigh’; common centipedegrass, Eremochloa ophiuroides (Munro) Hack; creeping bentgrass, Agrostis stolonifera L., ‘Crenshaw’.

Residues of legume crops used to increase soil fertility may also serve as sources of phytotoxins that can suppress the germination and early growth of weed and crop species. To test the hypothesis that weed and crop susceptibility to extracts of red clover shoots would be inversely proportional to seed mass, we (1) identified 18 weeds and 44 crops whose 100-seed masses ranged from 20 to 26,250 mg; (2) exposed their seeds in petri dishes and filter paper to a 2% aqueous extract of ‘Marathon’ red clover shoots or distilled water; and (3) measured germination percentage and radicle length of germinated seeds after incubation for 4 days. In a second experiment, we assessed germination and radicle growth of four crop and four weed species after exposure to 1% extracts of Marathon or ‘Cherokee’ red clover or distilled water. Germination inhibition by red clover extracts was greatest for lighter seeds and least for heavier seeds in Experiment 1 (P = 0.0005), but was unrelated to seed mass in Experiment 2. Radicle inhibition by red clover extracts was inversely proportional to seed mass in both Experiment 1 (P < 0.0001) and Experiment 2 (P = 0.0047), and, in Experiment 1, was greater for monocots than dicots (P = 0.0002). Our findings corroborate the general relationship between seed mass and stress tolerance observed by other investigators and indicate that small-seeded monocots are most likely to be susceptible to phytotoxins contained in red clover shoots.

Nomenclature: Red clover, Trifolium pratense L.

Field research was conducted to determine the potential of hyperspectral and multispectral imagery for late-season discrimination and mapping of grass weed infestations in wheat. Differences in reflectance between weed-free wheat and wild oat, canarygrass, and ryegrass were statistically significant in most 25-nm-wide wavebands in the 400- and 900-nm spectrum, mainly due to their differential maturation. Visible (blue, B; green, G; red, R) and near infrared (NIR) wavebands and five vegetation indices: Normalized Difference Vegetation Index (NDVI), Ratio Vegetation Index (RVI), R/B, NIR-R and (R − G)/(R G), showed potential for discriminating grass weeds and wheat. The efficiency of these wavebands and indices were studied by using color and color-infrared aerial images taken over three naturally infested fields. In StaCruz, areas infested with wild oat and canarygrass patches were discriminated using the indices R, NIR, and NDVI with overall accuracies (OA) of 0.85 to 0.90. In Florida–West, areas infested with wild oat, canarygrass, and ryegrass were discriminated with OA from 0.85 to 0.89. In Florida–East, for the discrimination of the areas infested with wild oat patches, visible wavebands and several vegetation indices provided OA of 0.87 to 0.96. Estimated grass weed area ranged from 56 to 71%, 43 to 47%, and 69 to 80% of the field in the three locations, respectively, with per-class accuracies from 0.87 to 0.94. NDVI was the most efficient vegetation index, with a highly accurate performance in all locations. Our results suggest that mapping grass weed patches in wheat is feasible with high-resolution satellite imagery or aerial photography acquired 2 to 3 wk before crop senescence.

Nomenclature: Wild oat (Avena fatua L. AVEFA and A. sterilis L. AVEST); canarygrass (Phalaris paradoxa L. PHAPA and P. minor Retz PHAMI); ryegrass, Lolium rigidum Gaudin LOLRI; wheat, Triticum durum L. ‘Mexicali.’

Weeds that respond more to nitrogen fertilizer than crops may be more competitive under high nitrogen (N) conditions. Therefore, understanding the effects of nitrogen on crop and weed growth and competition is critical. Field experiments were conducted at two locations in 1999 and 2000 to determine the influence of varying levels of N addition on corn and velvetleaf height, leaf area, biomass accumulation, and yield. Nitrogen addition increased corn and velvetleaf height by a maximum of 15 and 68%, respectively. N addition increased corn and velvetleaf maximum leaf area index (LAI) by up to 51 and 90%. Corn and velvetleaf maximum biomass increased by up to 68 and 89% with N addition. Competition from corn had the greatest effect on velvetleaf growth, reducing its biomass by up to 90% compared with monoculture velvetleaf. Corn response to N addition was less than that of velvetleaf, indicating that velvetleaf may be most competitive at high levels of nitrogen and least competitive when nitrogen levels are low. Corn yield declined with increasing velvetleaf interference at all levels of N addition. However, corn yield loss due to velvetleaf interference was similar across N treatments except in one site–year, where yield loss increased with increasing N addition. Corn yield loss due to velvetleaf interference may increase with increasing N supply when velvetleaf emergence and early season growth are similar to that of corn.

Nomenclature: Velvetleaf, Abutilon theophrasti Medic. ABUTH; corn, Zea mays L. ‘Pioneer 33A14’.

Large crabgrass, redroot pigweed, and hairy galinsoga are three important weed species in bell pepper and other crops in the northeastern United States. Field experiments were conducted in 1998 and 1999 to determine the influence of density and relative emergence time of the three weed species on bell pepper fruit yield. Densities of 0, 1, 2, 4, 8, 16, and 32 plants m⁻¹ row were established for each weed species from naturally occurring weed populations. The effects of relative emergence time were studied by investigating the different yield responses to weeds emerging at two different times: 3 d or 2 wk after transplanting of pepper. Both weed density and relative emergence time affected pepper yield loss. The relative competitive ability of weed species varied between years. Large crabgrass was the most competitive species in 1998 and the measure of yield loss at low weed densities, I, was estimated to be 34% on the basis of the nonlinear hyperbolic equation. Redroot pigweed was most competitive in 1999 with an estimate of 88% for I. Hairy galinsoga was the least competitive weed in both years. Maximum yield loss under 32 plants m⁻¹ row ranged from 19% with late-emerging hairy galinsoga in 1998 to 99% with early-emerging redroot pigweed in 1999. A new equation was proposed to characterize the relation between yield loss and weed pressure by expanding the nonlinear hyperbolic equation to include a parameter to account for the change of maximum yield loss with emergence time. The expanded equation generally provided a more accurate prediction of yield loss. In addition, several models are introduced to describe both the effects of density and relative emergence time of multiple weed species on crop yield. Generally these models provided an adequate fit of the data and a good description of the competitive ability of the mixed population.

Nomenclature: Hairy galinsoga, Galinsoga ciliata (Raf.) Blake, GASCI; large crabgrass, Digitaria sanguinalis (L.) Scop. DIGSA; redroot pigweed, Amaranthus retroflexus L. AMARE; bell pepper, Capsicum annuum L.

Because soil-residual PRE herbicides reduce and delay annual weed emergence and decrease later weed growth, susceptible weeds surviving or recovering from herbicide treatment reduce crop yields less than do untreated weeds. Recently, corn yields were shown to be reduced differently by untreated weeds emerging in and between crop rows. However, equations have not been reported before that relate corn yield to in-row and between-row weed cover of mixed weed populations recovering from PRE soil-residual herbicides. Published data from PRE herbicide screening research for 3 site-yr in Missouri were reanalyzed to characterize this relation. In-row and between-row weed cover of mixed weed populations, chiefly giant foxtail and common waterhemp, were measured from photographs at midsummer. In 2 of 3 site-yr and with the 3 site-yr average, corn yields were a nonlinear function of both in-row and between-row weed cover recovering from various PRE soil-residual herbicide treatments. In 1 of 3 site-yr, corn yields were a nonlinear function of only between-row total weed cover. Subdividing weed cover into in-row and between-row subpopulations in equations accounted for more data variability in yield estimates than including either subpopulation alone. For all 3 site-yr after PRE herbicide treatment, corn yields were a nonlinear function of only between-row visually rated total weed control. Visual evaluation was less sensitive than photographic weed cover for measuring the contribution of in-row weeds to corn yield loss and characterizing the functional form of the equations.

Nomenclature: Common waterhemp, Amaranthus rudis Sauer AMATA; giant foxtail, Setaria faberii Herrm. SETFA; corn, Zea mays L. ZEAMX ‘Pioneer 33G28’.

Weeds generally occur in patches in production fields. Are these patches spatially and temporally stable? Do management recommendations change on the basis of these data? The population density and location of annual grass weeds and common ragweed were examined in a 65-ha corn/soybean production field from 1995 to 2004. Yearly treatment recommendations were developed from field means, medians, and kriging grid cell densities, using the hyperbolic yield loss (YL) equation and published incremental YL values (I), maximum YL values (A), and YL limits of 5, 10, or 15%. Mean plant densities ranged from 12 to 131 annual grasses m⁻² and < 1 to 37 common ragweed m⁻². Median weed densities ranged from 0 to 40 annual grasses m⁻² and were 0 for common ragweed. The grass I values used to estimate corn YL were 0.1 and 2% and treatment was recommended in only 1 yr when the high I value and either the mean or median density was used. The grass I values used for soybean were 0.7 and 10% and estimated YL was over 10% all years, regardless of I value. The common ragweed I values were 4.5 and 6% for corn and 5.1 and 15.6% for soybean. On the basis of mean densities, fieldwide treatment would have been recommended in 6 of 9 yr but in no years when the median density was used. Recommendations on the basis of grid cell weed density and kriging ranged from > 80% of the field treated for grass weeds in 3 of 4 yr in soybean to < 20% of the field treated for common ragweed in 2002 and 2004 (corn). Grass patches were more stable in time, space, and density than common ragweed patches. Population densities and spatial distribution generally were variable enough so that site-specific information within this field would improve weed management decisions.

Nomenclature: Common ragweed, Ambrosia artimisiifolia L. AMBEL; corn, Zea mays L. ZEAMA; soybean, Glycine max L. Merr. GLYMX.

Clopyralid, picloram, triclopyr, metsulfuron, and tebuthiuron were applied to control kudzu on four loblolly pine forest regeneration sites during July 1997. Spot treatments were applied to recovering kudzu in June 1998 and June 1999. Soil leachate was monitored for these five herbicides from July 1997 to December 2000. All herbicides were detected in shallow (51–58 cm deep) and deep lysimeters (84–109 cm deep). Clopyralid was not persistent and limited leaching occurred, with residue levels of 0.4 to 2.8 μg L⁻¹ in 12 of 102 deep lysimeter samples. Picloram was mobile and persisted at 0.6 to 2.5 μg L⁻¹ in shallow and deep lysimeters for at least 10 mo after the initial application. Triclopyr residues were not persistent in shallow lysimeters and remained < 6 μg L⁻¹ during the study. Metsulfuron persisted at < 0.1 μg L⁻¹ for 182 to 353 d in shallow lysimeters and at < 0.07 μg L⁻¹ for 182 to 300 d in the deep lysimeters in various plots. Tebuthiuron peaks in the deep lysimeters ranged from 69 to 734 μg L⁻¹ 34 to 77 d after the first spot treatment. In the soil that was essentially a fill area, tebuthiuron residues remained > 400 μg L⁻¹ (402–1,660 μg L⁻¹) in the shallow lysimeter samples and > 180 μg L⁻¹ (181–734 μg L⁻¹) in the deep lysimeters throughout a 354-d period that followed the first spot application. When used as part of a forest regeneration program, the relative potentials of the herbicides to move into shallow groundwater were: tebuthiuron > picloram > metsulfuron > clopyralid > triclopyr.

Nomenclature: Clopyralid; metsulfuron; picloram; tebuthiuron; triclopyr; kudzu, Pueraria montana (Lour.) Merr. PUEMO; loblolly pine, Pinus taeda L. PINTA.