Seeds from natural populations of fierce thornapple and velvetleaf collected in a corn-growing area in central Spain were incubated at a range of constant temperatures and water potentials to model the progress of germination on the basis of the accumulation of hydrothermal time. Previous to the germination tests, the seeds were treated in two different ways: (1) dark storage under dry conditions (nonchilled seeds), and (2) burying in the original soil at 10-cm depth during 2 mo in winter (naturally chilled seeds). The results indicated different mechanisms inhibiting germination in both weed species. Whereas fierce thornapple displayed some type of embryo dormancy, the lack of germination in velvetleaf appeared to be entirely due to the seed coat. On the other hand, significant differences between nonchilled and naturally chilled seeds in fierce thornapple were observed, mainly due to the decrease in the mean base water potential of the 50th percentile in the latter, which indicated a loss of dormancy by exposure of the seeds to natural conditions. Hydrothermal time appears to be a good description of the germination patterns in both weed species, but in the case of fierce thornapple, only for naturally chilled seeds. Thus, the development of the hydrothermal model in fierce thornapple raises some questions for consideration concerning the influence of the type of seeds (conditions of storage, pretreatments of the seeds before germination tests) on its germination capacity.

Amicarbazone is a new triazolinone herbicide with a broad spectrum of weed control. The phenotypic responses of sensitive plants exposed to amicarbazone include chlorosis, stunted growth, tissue necrosis, and death. Its efficacy as both a foliar- and root-applied herbicide suggests that absorption and translocation of this compound is very rapid. This new herbicide is a potent inhibitor of photosynthetic electron transport, inducing chlorophyll fluorescence and interrupting oxygen evolution ostensibly via binding to the QB domain of photosystem II (PSII) in a manner similar to the triazines and the triazinones classes of herbicides. As a result, its efficacy is susceptible to the most common form of resistance to PSII inhibitors. Nonetheless, amicarbazone has a good selectivity profile and is a more potent herbicide than atrazine, which enables its use at lower rates than those of traditional photosynthetic inhibitors.

Bispyribac-sodium selectively controls annual bluegrass in creeping bentgrass and perennial ryegrass, which might be attributed to differential metabolism among species. To test this hypothesis, we investigated metabolism of 14C-bispyribac-sodium in annual bluegrass, creeping bentgrass, and perennial ryegrass. Creeping bentgrass and perennial ryegrass metabolized approximately 50% of the 14C-bispyribac-sodium after 1 d, while annual bluegrass metabolized less than 20%. Parent herbicide recovered 7 d after treatment in annual bluegrass, creeping bentgrass, and perennial ryegrass was 73, 32, and 39% of total radioactivity per species, respectively. Polar metabolites recovered after 7 d in annual bluegrass, creeping bentgrass, and perennial ryegrass were 24, 59, and 55% of total radioactivity per species, respectively. Half-life of 14C-bispyribac-sodium in annual bluegrass, creeping bentgrass, and perennial ryegrass was estimated at greater than 7 d, 1 d, and 2 d, respectively. Results support the hypothesis that differential tolerances of these grasses are attributed to herbicide metabolism.

Growers of glyphosate-resistant crops apply micronutrients tank-mixed with glyphosate to save time and production costs. Therefore, effect of zinc (Zn), as Zn sulfate, on absorption, translocation, and efficacy of glyphosate on yellow nutsedge was investigated. Glyphosate at 850 g ae ha−1 provided 90% yellow nutsedge control at 5 wk after treatment (WAT). Presence of Zn at 1,000 ppmw in the glyphosate spray solution reduced yellow nutsedge control to 24 and 8%, 3 and 5 WAT, respectively. Yellow nutsedge control decreased with increasing Zn level (500 to 2,000 ppmw) in the spray solution. Yellow nutsedge treated with higher rates of Zn tank-mixed with glyphosate produced more tubers and tillers per plant than untreated plants. An abrupt decrease in absorption and translocation of 14C–glyphosate occurred between 500 and 1,000 ppmw Zn. The antagonistic effect of Zn on glyphosate depended mainly on reduced absorption and translocation of 14C–glyphosate within treated tissues. Less than 10% of applied 14C–glyphosate was absorbed when glyphosate was mixed with 1,000, 2,000, or 4,000 ppmw Zn as compared with 85% absorption for glyphosate alone. These treatments inhibited > 90% of 14C–glyphosate translocation out of the treated leaf and > 50% of tuber translocation relative to glyphosate alone. Results indicate that micronutrients containing Zn are not suitable for tank-mixing with glyphosate.

Japanese knotweed is an aggressive alien species in Europe, North America, and Australia, causing a range of environmental problems. Eradication of Japanese knotweed is proving to be a difficult task, because the plant is able to propagate generatively by intra- and interspecific hybridization, and vegetatively from shoot and tiny rhizome pieces. Despite the economic consequences of Japanese knotweed on natural and built environments, its physiology is not yet fully understood; especially important are sink-source relations between old and young parts of the rhizome and growth of lateral and latent rhizome buds. Current methods of chemical control include three types of phloem-mobile herbicides, such as glyphosate, imazapyr, and synthetic auxins. These herbicides have limitations on their use, and all fail to eradicate the plant completely, for the reasons discussed in this review. Our aim is to suggest prospective approaches to enable chemical eradication: use of signals to induce controlled growth and development of quiescent rhizome buds; use of phytohormones, sugars, and light to increase allocation of phloem-mobile herbicides to the rhizome; use of xylem-mobile herbicides to exterminate the old rhizome parts; and use of different phloem-mobile herbicides at different growth stages.

Synthetic seed banks are a useful tool for tracking how weed populations change over time. By sowing a known number of seeds of a given species within a quadrat with defined boundaries, an investigator can measure the number remaining and thereby calculate demographic rates (e.g., mortality). The alternative is to use in situ seeds and estimate their initial population density via sampling. To make a synthetic seed bank approach useful within an agricultural system subjected to soil disturbances such as tillage, one would need a way to account for seeds leaving the initial quadrat (i.e., a way to follow how the area encompassing the sown seeds changes over time). Without accounting for the change in location/extent of the synthetic seed bank, any field operation moving soil will create additional uncertainty in population size. Depending on the “aggressiveness” of specific field operations and the initial size of the quadrat, this effect might be negligible or so large as to be intractable. Here, we describe a method for following a synthetic seed bank over time using a “living boundary” of nondormant seeds, which effectively play the role of tracers used in the study of dynamics in other scientific disciplines. Study quadrats in East Lansing, MI, and Arlington, WI, were sown with giant foxtail and velvetleaf at a rate of 2,000 seeds m−2. The study quadrats were marked on the perimeter and diagonals using nondormant seeds of three marker species: kale, radish, and rye. The areas were then subjected to tillage and planting operations. Spatial coordinates of seedling locations for the marker and weed species were obtained through digital image processing. A nonparametric comparison of the spatial displacement of marker and weed species indicated that their empirical spatial distributions did not differ. The marker species quadrats described by the 50th, 90th, and 99th quantiles of movement contained all velvetleaf seedlings in Wisconsin, all velvetleaf seedlings in Michigan, and all giant foxtail seedlings in Michigan, respectively. The results suggest a simple rule for applying the method to field demography studies: after the original quadrat is deformed and seedlings have emerged, flag the polygon containing all marker seedlings to obtain the expanded quadrat containing the study weed population.

Soybean is a major crop cultivated in Brazil, and acetolactate synthase (ALS)-inhibiting herbicides are widely used to control weeds in this crop. The continuous use of these ALS-inhibiting herbicides has led to the evolution of herbicide-resistant weeds worldwide. Greater beggarticks is a polyploid species and one of the most troublesome weeds in soybean production since the discovery of ALS-resistant biotypes in 1996. To confirm and characterize the resistance of greater beggarticks to ALS inhibitors, whole-plant bioassays and enzyme experiments were conducted. To investigate the molecular basis of resistance in greater beggarticks the ALS gene was sequenced and compared between susceptible and resistant biotypes. Our results confirmed that greater beggarticks is resistant to ALS inhibitors and also indicated it possesses at least three isoforms of the ALS gene. Analysis of the nucleotide and deduced amino acid sequences among the isoforms and between the biotypes indicated that a single point mutation, G–T, in one ALS isoform from the resistant biotype resulted in an amino acid substitution, Trp574Leu. Two additional substitutions were observed, Phe116Leu and Phe149Ser, in a second isoform of the resistant biotype, which were not yet reported in any other herbicide-resistant ALS gene; thus, their role in conferring herbicide resistance is not yet ascertained. This is the first report of ALS mutations in an important, herbicide-resistant weed species from Brazil.

Exotic weeds can interfere with neighboring species by releasing allelochemicals that either directly inhibit growth and distribution of associated species or affect them indirectly by disrupting their interaction with soil organisms, such as arbuscular mycorrhizal fungi (AMF). The allelopathic potential of tall hedge mustard was assessed using aqueous root and shoot extracts in seed germination and radicle growth bioassays. Aqueous tall hedge mustard root and shoot extracts strongly inhibited seed germination and growth of bluebunch wheatgrass, Idaho fescue, and spotted knapweed, but had minimal autotoxicity. Chemical analysis of tall hedge mustard tissues revealed the presence of two major glucosinolates—isopropyl and sec-butyl glucosinolate. The degradation products of these glucosinolates (isopropyl isothiocyanate and sec-butyl isothiocyanate) were identified in dichloromethane extracts of tall hedge mustard aqueous root and shoot extracts. Commercially available isopropyl isothiocyanate and sec-butyl isothiocyanate inhibited seed germination and radicle growth, suggesting their role in the allelopathic potential of tall hedge mustard. Tall hedge mustard aqueous extracts and isothiocyanates incorporated into an agar medium inhibited the spore germination of the AMF, Glomus intraradices. Tall hedge mustard infestations were also found to reduce the AMF inoculum potential of soil under field conditions. The results from this study show that tall hedge mustard produces chemicals that can inhibit the growth of neighboring plant species and their AMF associates.

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

To assess the influence of long-term fertilization on weed communities of early and late rice crops, the weed species composition was investigated in experimental plots initiated in 1981 at the Key Field Experimental Monitoring Station of the Reddish Paddy Soil Eco-Environment in Wangcheng, China. The treatments were (1) a control (CK), no fertilizer; (2) N–P, no K; (3) N–K, no P; (4) P–K, no N; (5) N–P–K; (6) N–P–K + Ca, N, P, and K plus lime; (7) N–P + S, N and P plus additional rice straw return; (8) N–P–K + S, N, P, and K plus additional rice straw; (9) N–K + M, N and K plus swine manure. The results indicated that weed flora composition and density were influenced by the different fertilization treatments. Multivariate analyses indicated that changes in the weed community composition were primarily due to soil-available N, followed by light intensity on the field surface, and soil-available P. More weed species and total weed density were observed in the control and P–K plots than in plots in which N, P, and K were applied together. Omission of N application had a greater effect on the weed community than the omission of P or K applications. Nutrients derived from synthetic fertilizers and organic manure or the additional application of lime had no obvious effect on the weed community of late rice crops.

The development of fluridone resistance by hydrilla has significantly impacted hydrilla management, and research is ongoing to develop alternate herbicides for effective hydrilla control. We determined the potential cross-resistance in fluridone-resistant hydrilla to other bleaching herbicides norflurazon, mesotrione, and topramezone-methyl. Phytoene, β-carotene, and chlorophyll contents as a function of hydrilla biotype and herbicide treatment were evaluated. Hydrilla shoot tips were collected from fluridone-susceptible (S) and -resistant (R) biotypes and exposed to 5, 25, 50, 75, and 100 µg L−1 of herbicide. The susceptible biotype showed an increase in phytoene and a decrease in β-carotene and chlorophyll contents when treated with 5 µg L−1 fluridone, whereas higher doses of fluridone were required to affect these pigments in the resistant biotype. There was no difference in response by S and R biotypes to mesotrione and topramezone-methyl, with both biotypes showing significant affects on pigment contents at 5 µg L−1. Higher doses of norflurazon were required to affect these pigments in the R compared to the S biotype. The S biotype had EC50 values of 11.7, 12.2, and 4.7 µg L−1, whereas the R biotype had EC50 values of 56.6, 41.1, and 41.7 µg L−1 fluridone for phytoene, β-carotene, and chlorophyll contents, respectively. There was no difference in EC50 for phytoene, β-carotene, and chlorophyll values between the hydrilla biotypes for mesotrione and topramezone-methyl herbicides. In fluridone-susceptible and -resistant hydrilla biotypes, EC50 values for phytoene, β-carotene, and chlorophyll were 12.4 to 11.8, 10.2 to 13.2, and 3.1 to 4.6 µg L−1 mesotrione and 12.6 to 13.5, 13.3 to 11.9, and 4.6 to 5.7 µg L−1 topramezone-methyl, respectively. For norflurazon, S and R biotypes had EC50 values of 33.1, 45.4, and 40.6 µg L−1 and 84.6, 81.0, and 92.7 µg L−1 for phytoene, β-carotene, and chlorophyll, respectively. These studies confirmed negative cross-resistance of fluridone-resistant hydrilla to mesotrione and topramezone-methyl and a positive cross-resistance to norflurazon.

Crofton weed is a noxious invasive weed worldwide. However, the mechanisms underlying its invasiveness are still not well understood. We hypothesize that genetic differentiation and plasticity may help the plant invade heterogeneous habitats. To test this hypothesis, we compared the differences in seed morphometric and germination traits among 14 populations of the plant located at different elevations (640–2,430 m) in south Yunnan Province of southwest China. Germination capacity (GC) and index (GI) were markedly different among the 14 populations at the same temperature or water treatment. The results indicated genetic differentiations in these traits; maternal effects were not excluded. GC and GI were also different for each population across temperature or water treatments, showing phenotypic plasticity. Croton weed seed size and weight also responded genetically or plastically (or both) to different elevations. Seed width, weight, GC, and GI at each temperature increased with the increase of the elevation of origin, showing clinal variation patterns that reveal local adaptations to habitats encountered by the plant. The large seeds, high GC, and high GI could improve emergence, establishment, growth, and survival of seedlings at high elevation; the low GI could prevent seed germination before the onset of the rainy season at low elevation. On the basis of the results, genetic differentiation and plasticity in seed size and germination traits may help crofton weed acclimate to different elevations, facilitating its invasiveness.

The compositions of the germinable weed seedbank and aboveground weed communities in a long-term tillage and rotation study were characterized 4, 5, and 6 yr (2002 to 2004) after the adoption of glyphosate-tolerant corn and soybean. Averaged across rotation, mean germinable weed seed density and diversity were greatest in the no-tillage treatment as compared to the minimum- and conventional-tillage treatments. Averaged over tillage, density and diversity were greater in the corn–oat–hay (ryegrass + alfalfa) system as compared to the continuous corn and corn–soybean rotations. Similar trends in density and diversity were observed for the aboveground weed communities. Differences in community composition among treatments were quantified with the use of a multiresponse permutation procedure. Results indicated that the weed seedbank community in a corn–oat–hay rotational system differed from the communities associated with the continuous corn and corn–soybean rotational systems. Weed seedbank communities developing under a no-tillage operation differed from those in minimum- and conventional-tillage scenarios. Compositional differences among the aboveground weed communities were less pronounced in response to tillage and rotation. Indicator species analyses indicated that the number of significant indicator weed species was generally higher for no tillage than minimum or conventional tillage for both the seedbank and the aboveground weed communities. The number of significant indicator species for the seedbank and weed communities was generally greater in the three-crop rotation as compared to the continuous corn and corn–soybean rotations. The trends observed in density, diversity, and community composition after the adoption of glyphosate-tolerant corn and soybeans, and a glyphosate-dominated weed management program, were also observed when soil-applied herbicides were included in the study. We suggest that the switch to a POST-glyphosate protocol did not significantly alter weed communities in the short term in this study.

The commercialization of imazethapyr-resistant (Clearfield™, CL) rice in the southern United States has raised serious concerns about gene flow to red rice, producing imazethapyr-resistant red rice populations. Our objectives were to determine the impact of planting date, CL cultivars, and red rice biotypes on outcrossing rate; and to investigate the relative contribution of flowering time of CL rice and red rice biotypes, together with air temperature and relative humidity (RH), on outcrossing rate. Field experiments were conducted at Stuttgart, Rohwer, and Kibler, AR, from 2005 to 2007, at three or four planting times from mid-April to late May. ‘CL161’ (inbred cultivar) and ‘CLXL8’ (hybrid) rice were planted in nine-row plots, with red rice planted in the middle row. Twelve red rice biotypes were used. The flowering of red rice and CL rice, air temperature, and RH were recorded. Red rice seeds were collected at maturity. To estimate outcrossing rate, resistance to imazethapyr was evaluated in subsequent years and confirmed using rice microsatellite markers. CLXL8 rice flowered 2 to 4 d earlier than CL161 rice, and flowering was completed within 1 wk in all plantings. The flowering duration of most red rice biotypes ranged from 4 to 17 d. Flowering synchrony of red rice biotypes and CL rice ranged from 0 to 100% at different plantings. In general, CLXL8 had greater flowering overlap and higher outcrossing rate with red rice than did CL161 rice. The outcrossing rate of red rice biotypes ranged from 0 to 0.21% and 0 to 1.26% with CL161 and CLXL8 rice, respectively. The outcrossing rate differed within each planting date (P < 0.05). Outcrossing was generally lower in mid-May and late May than in mid-April and late April planting times. Flowering synchrony and outcrossing rate were not correlated (r2 < 0.01). Outcrossing with CL161 was primarily influenced by red rice biotype. A minimum air temperature of > 24 C in the evening also favors outcrossing with CL161. With CLXL8 rice, outcrossing was most affected by RH. When RH was < 54%, outcrossing was less (0.12%) than when RH was ≥ 54% (0.38%). With CLXL8 rice, a minimum RH of ≥ 54%, from mid-morning to noon, increased outcrossing with red rice. To fully understand the interaction effects of these factors on outcrossing with red rice, controlled experiments are needed.

Recent advances in molecular methods and statistical analyses provide weed scientists with powerful tools for examining the genetic structure of weedy plant populations. The value of these studies depends on effective sampling protocols; however, there is little consensus on how to sample plant populations for genetic diversity analyses. In this review, we draw on published literature that incorporates sampling theory and spatial statistics in population genetic analyses to identify key factors to consider when designing a sampling strategy. We discuss how sampling design is affected by research objectives, biology of the study species, population structure, marker choice, and the genetic parameters to be investigated, and we offer suggestions on defining sampling units and developing sampling protocols.

Research was conducted to determine the competitiveness and fitness of a protoporphyrinogen oxidase (protox)-resistant common waterhemp biotype. Protox-resistant and protox-susceptible biotypes were grown under noncompetitive and competitive arrangements in the greenhouse. In the noncompetitive study, a single plant of each biotype was planted separately in 15-cm-diam pots. Photosynthesis, leaf area, and plant biomass were measured 10, 20, 30, and 40 d after transplanting (DATP). In general, photosynthesis rate and plant biomass were similar between biotypes. However, the protox-resistant biotype had higher leaf area than the susceptible biotype at 20, 30, and 40 DATP. A replacement series study was conducted in the greenhouse to evaluate the relative competitiveness of protox-resistant and protox-susceptible common waterhemp. Photosynthesis, leaf area, plant height, and plant biomass were measured 7, 14, 21, and 28 DATP. Protox-resistant and -susceptible common waterhemp were equally competitive 28 DATP. Relative crowding coefficient values 28 DATP were 0.86, 0.89, 1.09, and 1.13 for photosynthesis, leaf area, plant height, and plant biomass, respectively. This suggests protox-resistant and -susceptible common waterhemp were equally competitive and the frequency of protox-resistant biotype is unlikely to decrease in the absence of protox–herbicide selection pressure.

Palmer amaranth is resistant to several herbicides, including glyphosate, and there is concern that the resistance traits can be transferred between spatially segregated populations via pollen movement. The objective of this study was to describe the physical properties of Palmer amaranth pollen, specifically size, density, and settling velocity (Vs), that influence pollen flight. The mean diameter for Palmer amaranth pollen, as determined by light microscopy, was 31 µm (range of 21 to 38 µm); mean pollen diameter as measured with the use of an electronic particle sizer was 27 µm (range of 21 to 35 µm). The mean density of the solid portion of the pollen grain was 1,435 kg m−3. Accounting for the density of the aqueous fraction, the mean density of a fully hydrated pollen grain was 1,218 kg m−3. By Stokes's law, the estimated mean theoretical Vs for individual Palmer amaranth pollen grains was 3.4 cm s−1 for the range of pollen diameters with a mean of 31 µm and 2.6 cm s−1 for the range of pollen diameters with a mean of 27 µm. Results from laboratory studies indicated the majority of single pollen grains settled at a rate of 5.0 cm s−1. The difference between the theoretical and empirical estimates of Vs was likely due to changes in pollen density and shape postanthesis, which are not accounted for using Stokes's law, as well as the presence pollen clusters.

Theory and models of crop yield loss from weed competition have led to decision models to help growers choose cost-effective weed management. These models are available for multiple-species weed communities in a single season of several crops. Growers also rely on crop rotation for weed control, yet theory and models of weed population dynamics have not led to similar tools for planning of crop rotations for cost-effective weed management. Obstacles have been the complexity of modeling the dynamics of multiple populations of weed species compared to a single species and lack of data. We developed a method to use limited, readily observed data to simulate population dynamics and crop yield loss of multiple-species weed communities in response to crop rotation, tillage system, and specific weed management tactics. Our method is based on the general theory of density dependence of plant productivity and extensive use of rectangular hyperbolic equations for describing crop yield loss as a function of weed density. Only two density-independent parameters are required for each species to represent differences in seed bank mortality, emergence, and maximum seed production. One equation is used to model crop yield loss and density-dependent weed seed production as a function of crop and weed density, relative time of weed and crop emergence, and differences among species in competitive ability. The model has been parameterized for six crops and 15 weeds, and limited evaluation indicates predictions are accurate enough to highlight potential weed problems and solutions when comparing alternative crop rotations for a field. The model has been incorporated into a decision support tool for whole-farm management so growers in the Central Great Plains of the United States can compare alternative crop rotations and how their choice influences farm income, herbicide use, and control of weeds in their fields.

Cadillo is an invasive species commonly found in pastures, rangelands, and disturbed areas. It is becoming a significant problem weed in Florida pastures and natural areas. The objectives of this research were to determine effective techniques to break seed dormancy and the effect of light, temperature, pH, water stress, and depth of seed burial on Cadillo germination. Cadillo seeds had significant levels of innate dormancy imposed by a hard seed coat; chemical scarification was the most effective technique for removing dormancy. Seeds germinated from 15 to 40 C, with an optimal temperature of 28 C. Germination was unaffected by pH levels. Water stress below −0.2 MPa reduced seed germination. Cadillo germination was not light-dependent and seeds emerged from depths up to 9 cm, with the greatest occurring emergence near the soil surface. Considering that Cadillo seed can germinate under a wide range of environmental conditions, it is not surprising that it has become a serious invasive weed in Florida.

A greenhouse study was conducted to determine the influence of soybean cyst nematode (SCN) –susceptible and –resistant plant combinations on SCN population densities and plant growth. Purple deadnettle, annual ryegrass, SCN-resistant and -susceptible soybean were planted in pots alone or in combination at one plant pot−1. Annual ryegrass and purple deadnettle reduced soybean growth. Pots with SCN-resistant plants had lower numbers of SCN cysts and eggs than pots with SCN-susceptible plants. However, an SCN-susceptible species grown with any of the SCN-resistant plants resulted in higher cyst counts than pots with only SCN-resistant plants. From an SCN management standpoint, this research suggests that there may be no incentive to using annual ryegrass as a cover crop over planting other SCN-resistant crops to reduce SCN population density.