Anoda cristata control with glyphosate in narrow- and wide-row soyabean

Experiments evaluated the effect of glyphosate rate and Anoda cristata density, on crop and weed biomass and weed seed production in wide (70 cm) and narrow rows (35 cm) glyphosate‐resistant soyabean (Glycine max). Soyabean density was higher at 35 cm row spacing as an increase in planting rate in narrow‐row soyabean is recommended for producers in Argentina. Soyabean biomass at growth stage V4 (four nodes on the main stem with fully developed leaves beginning with the unifoliate leaves) was higher when grown on narrow than in wide‐rows but was not affected by the presence of A. cristata. At growth stage R5 (seed initiation – seed 3 mm long in a pod at one of the four uppermost nodes on the main stem, with a fully developed leaf and full canopy development), crop biomass was greater in narrow rows compared with wide rows with 12 plants m^?2 of A. cristata. In narrow‐row soyabean, a single application of a reduced rate of glyphosate maintained soyabean biomass at R5 and provided excellent weed control regardless of weed density. In wide‐row soyabean control was reduced at the high weed density. Regardless of row spacing, A. cristata biomass and seed production were severely reduced by half of the recommended dose rate of glyphosate but the relationship between biomass and seed production was not altered. Glyphosate rates as low as 67.5 g a.e. ha^?1 in narrow rows or 540 g a.e. ha^?1 in wide rows provided excellent control of A. cristata. To minimize glyphosate use, planting narrow‐row soyabean are effective where A. cristata density is low.     

Consequences of narrow crop row spacing and delayed Echinochloa colona and Trianthema portulacastrum emergence for weed growth and crop yield loss in maize

Echinochloa colona and Trianthema portulacastrum are weeds of maize that cause significant yield losses in the Indo‐Gangetic Plains. Field experiments were conducted in 2009 and 2010 to determine the influence of row spacing (15, 25 and 35 cm) and emergence time of E. colona and T. portulacastrum (0, 15, 25, 35, 45 and 55 days after maize emergence; DAME) on weed growth and productivity of maize. A season‐long weed‐free treatment and a weedy control were also used to estimate maize yield and weed seed production. Crop row spacing as well as weed emergence time had a significant influence on plant height, shoot biomass and seed production of both weed species and grain yield of maize in both years. Delay in emergence of weeds resulted in less plant height, shoot biomass and seed production. However, increase in productivity of maize was observed by delay in weed emergence. Likewise, growth of both weed species was less in narrow row spacing (15 cm) of maize, as compared with wider rows (25 and 35 cm). Maximum seed production of both weeds was observed in weedy control plots, where there was no competition with maize crop and weeds were in rows 35 cm apart. Nevertheless, maximum plant height, shoot biomass and seed production of both weed species were observed in 35 cm rows, when weeds emerged simultaneously with maize. Both weed species produced only 3–5 seeds per plant, when they were emerged at 55 DAME in crop rows spaced at 15 cm. Infestation of both weeds at every stage of crop led to significant crop yield loss in maize. Our results suggested that narrow row spacing and delay in weed emergence led to reduced weed growth and seed production and enhanced maize grain yield and therefore could be significant constituents of integrated weed management strategies in maize.     

Weed seed decay in conventional and diversified cropping systems

Diversified cropping systems can have high soil microbial biomass and thus strong potential to reduce the weed seedbank through seed decay. This study, conducted in Iowa, USA, evaluated the hypothesis that weed seed decay is higher in a diversified 4‐year maize–soyabean–oat/lucerne–lucerne cropping system than in a conventional 2‐year maize–soyabean rotation. Mesh bags filled with either Setaria faberi or Abutilon theophrasti seeds and soil were buried at two depths in the maize phase of the two cropping systems and sampled over a 3‐year period. Setaria faberi seed decay was consistently greater at 2 cm than at 20 cm burial depth and was higher in the more diverse rotation than in the conventional rotation in 1 year. Abutilon theophrasti seeds decayed very little in comparison with seeds of S. faberi. Separate laboratory and field experiments confirmed differences in germination and seed decay among the seed lots evaluated each year. Fusarium, Pythium, Alternaria, Cladosporium and Trichoderma were the most abundant genera colonising seeds of both species. A glasshouse experiment determined a relationship between Pythium ultimum and S. faberi seed decay. Possible differences in seed susceptibility to decay indicate the need to evaluate weed seedbank dynamics in different cropping systems when evaluating overall population dynamics and formulating weed management strategies.     

Predispersal seed predation of Amaranthus retroflexus and Chenopodium album growing in soyabean fields

Field experiments were made in 1998 and 1999 to determine the influence of tillage and soyabean (Glycine max) row width on predispersal weed seed predation in Amaranthus retroflexus L. (redroot pigweed) and Chenopodium album L. (common lambsquarters). Soyabean was planted in wide (76 cm) and narrow (19 cm) rows with conventional or conservation tillage. Additional control plots without soyabean were also established. The two objectives were to determine (1) whether predispersal seed predation occurs in A. retroflexus or C. album, and (2) whether disturbance (soil tillage) or microclimate (planting pattern) influence predation level. Mean rates of seed predation were 26% and 4% in A. retroflexus and C. album, respectively. Although these levels were low at the population level, individual plants of both species had predation levels ranging from 0% to 80%, however, very few individuals of C. album had levels of predation above 10%. Differences among tillage and row width treatments occurred for A. retroflexus, but not for C. album. Amaranthus retroflexus and C. album growing within the soyabean crop received less light than those in the no‐crop plots, and produced less above‐ground biomass, smaller terminal inflorescences, and fewer seeds per inflorescence. Plant height, terminal inflorescence weight, and total seeds were correlated with predation in both weed species.     

Effects of crop management practices on Echinochloa crus-galli and Chenopodium album seed production in a maize/soyabean rotation

Seed production of residual weed populations needs to be taken into account when estimating the long-term impact of low-input agronomic practices. The objective of this study was to measure the effects and interactions of crop, weed control, tillage practice and nutrient source on the seed production of the dominant residual weed species in a maize/soyabean rotation at two sites: Echinochloa crus-galli (L.) Beauv. on a Sainte-Rosalie clay and Chenopodium album L. on a Duravin clay loam. Seed production per unit area was estimated in each experimental unit. Weed seed production was greater under mechanical weed control compared with chemical weed control. In 1997, E. crus-galli seed production reached over 326 000 seeds m^–2 in mechanical weed control treatments, but averaged less than 500 seeds m^–2 in the chemical weed control treatments. Chenopodium album produced in the range of 766 000 and 73 000 seeds m^–2 in mechanical and chemical weed control treatments respectively. Very few or no weed seeds were produced in soyabean under chemical control. Tillage intensity and nutrient source did not affect seed production of either weed species, with the exception that E. crus-galli produced more seeds in chisel than in mouldboard plough tillage in soyabean. Weed control method had more impact on seed production than tillage intensity and nutrient source in a maize/soyabean rotation.     

Phalaris minor seedbank studies: longevity, seedling emergence and seed production as affected by tillage regime

Studies were conducted to investigate seed longevity, seedling emergence and seed production of the weed Phalaris minor in wheat in northern India. The longevity of P. minor seeds buried in bags in the field was often limited to less than 1 year, although many seeds buried at 30 cm depth in a rice–wheat rotation remained viable for longer. The application of direct seeding in wheat reduced the seedling emergence rate of P. minor , when compared with conventional ploughing and sowing. However, a larger P. minor seedbank in the upper soil layer in plots under direct seeding partly reversed this positive effect in one of the two studies. Besides differences in relative distribution of weed seeds through the soil profile, it was likely that other factors such as reduced soil disturbance and soil characteristics associated with the application of direct seeding were also involved in regulating the emergence rate. Mature P. minor plants in wheat were found to invest a stable part (27%) of their aboveground biomass in seed, so that total seed weight was strongly linearly correlated with the aboveground biomass of the mother plant. Individual seed weight, however, was little affected by the weight of the mother plant.     

Digitaria sanguinalis seed dormancy release and seedling emergence are affected by crop canopy and stubble

Digitaria sanguinalis is a troublesome annual weed that causes important yield losses in different crops. Despite this, there is scarce information about different aspects of its biology under field conditions. New knowledge about the establishment process of this species will be of paramount importance in order to maximise the effectiveness of weed management. The aims of this paper were to evaluate the effect of stubble found on the surface on seed dormancy levels through the season, the effects of stubble and soyabean crop canopy on seedling emergence and to determine the field emergence pattern as a consequence of seed dormancy level at dispersal time. Seeds on the soil surface, which showed a high dormancy level at the beginning of autumn, were released from dormancy by low winter temperatures and germinated during spring as temperatures rose, showing a transient surface seedbank. Seeds covered by stubbles had delayed the emergence in the field due to lower alternating temperatures perceived by the surface seedbank. On the other hand, the presence of a soyabean crop and stubble together reduced the number of seedlings. Seeds with a high dormancy level at dispersal time showed a delayed emergence in the next season when compared with seeds with a lower dormancy level. However, the final number of seedlings was similar. Both stubble on surface and crop canopy are useful factors to lessen and delay the seedling emergence allowing the design of weed management strategies in order to diminish the population levels of this species.     

Reducing intrarow weed numbers in row crops by means of a biennial cultivation system

Intrarow weed emergence in row crops can be reduced by means of a biennial cultivation system that is based on an exhaustion of the weed seedbank in the upper soil layer of crop‐free bands established in a preceding cereal crop, year I, before the row crop, year II. In this study, a series of field experiments is presented focusing more specifically on the influence of prevention of weed seed shedding and of different cultivation tactics in the system on intrarow weed emergence in the bands in year II. As the system excludes inverting soil tillage between years I and II, the prevention of weed seed shedding in year I turned out to be a key factor in achieving the desired effect of the system. This was seen with spring barley grown in year I, but not with winter wheat, where the system actually resulted in an increase in intrarow weed numbers in spite of the measures taken in year I. Cultivating the crop‐free bands in spring barley in year I with conventional goose‐foot shares in order to enhance seed germination and mortality further had no significant effects regardless of time and intensity. Results from two other experiments, in which freshly shed weed seeds were incorporated into the soil, supported the finding that cultivating the bands was of no advantage.     

Modelling population dynamics of Sinapis arvensis in organically grown spring wheat production systems

Although we know that alterations in crop density, crop spatial pattern and inclusion of more selective weed control can improve weed suppression for organic growers, it is unknown whether these result in changes to the weed seedbank that increase cropping system profitability over time. Data collected from field trials conducted in 2009 and 2010 in Maine, USA, comparing regional grower practices (Standard) with management that aimed to (i) facilitate better physical weed control through the use of wide row spacing and inter‐row cultivation (Wide) or (ii) enhance crop–weed competition through increased seeding rate and narrow inter‐row spacing (Narrow HD), were used to construct a matrix population model with an economic sub‐model. Using field measurements of grain yield and weed survival and fecundity, we investigated the lasting implications of employing alternative organic spring wheat (Triticum aestivum) production practices on Sinapis arvensis population dynamics. In most scenarios, the model indicated that regional production practices were not sufficient to prevent an increase in the weed seedbank, even with excellent weed control. The two alternative methods, on the other hand, were able to limit weed population growth when initial densities were low or cultivation efficacy was >80%. Due to higher seed costs in the Narrow HD system, net returns were still lower after 10 years of simulation in this system compared with wide rows with cultivation, despite a lower weed seedbank.     

The role of arable weed seeds for agroecosystem functioning

A literature study was conducted to gather knowledge on the impact of weed seeds on agroecosystem functioning other than effects related to the production of weed seedlings and plants. The results of the review suggested that a larger and more diverse weed seedbank can contribute to the biodiversity of various groups of macrofauna and microbiota, with a positive or negative impact on the agroecosystem. However, relationships between weed seed availability and functional biodiversity in the field have generally not been established, with the exception of case studies of seeds sustaining populations of granivorous farmland birds or acting as reservoirs and vectors of plant pathogens. To value the contribution of different weed seeds to sustaining populations of functional biota, more detailed information on their relationships with seeds is essential. Hypotheses and related questions that can be used to explore the impact of weed seeds on functional biodiversity have been identified. The identification of weed seed species that are a key to sustaining functional biota may lead to a weed management strategy aiming to minimise the damage of weeds to crops while taking the alternative ecological roles of weed seeds into account.     

Tumbleweeds in the Western Australian cropping system: seed dispersal characteristics of Salsola australis

Salsola australis, like other agricultural weed species of the Salsola genus, produces a mobile seedbank. Aspects of this mobile seedbank were investigated in three field trials, including total seed production, rate of seed shedding, rate at which seeds lose germinability and the distance and directionality of plant movement. Total seed production was highly variable (ranging from 138 to 7734 seeds per plant), but was directly related to aboveground plant biomass at maturity. Following senescence, mature plants broke free of their root system and the wind driven plants moved considerable distances (1.6–1247.2 m). Half of the mobile plants moved <100 m, as they became entangled with other S. australis plants within the stand. Seed shedding commenced before the plants became mobile and increased with movement, but was also related to the aging and weathering processes experienced by stationary or mobile plants. All plants retained a proportion of their seed in spite of movement, weathering and ageing of the plants, although germinability of retained seed dropped to <2% after 2 months. Salsola australis engages in broad scale seed dispersal similar to that observed in other species of the Salsola genus, allowing this species to maintain a high rate of invasion and range expansion.     

The demography of Datura ferox (L.) in soybean crops

The emergence, survival, seed production and seed dispersal of Datura ferox was studied in soybean fields in 1982–1983 and 1984–1985. Most seedling emergence occurred within one month of crop sowing. Later germination, associated with inter-row cultivation, represented 4–26% of the total seedlings, and none survived to seed production. Only 5% of the first cohort in 1982–1983, and 7% in 1984–1985, survived to seed production; it was independent of initial density. Although weed density was greatly reduced by control measures, negative relationships were observed between peak seedling density and plant height, stem diameter, number of ramifications, number of reproductive structures and seed production per plant. Only a small proportion of seeds (about 1%) were shed prior to soybean harvest. Combine harvesters collected more than 90% of capsules, but between 7% and 40% of the seeds were returned to the field. Seed viability was unaffected by passing through the machine. The patterns of seed dispersal varied depending on the design of the combine harvester. Two models shed seeds between 0 m and 21 m from their source, but another shed seeds between 0 m and 98 m. Calculations, based in life history parameters, showed that weed seed production would increase more rapidly if the seeds were dispersed during crop harvesting than if they arc not, even when the return of seeds to the soil by the combine is not large.     

A mathematical model to predict the population dynamics of Oryza sativa var. sylvatica

A mathematical model has been developed for the prediction of the population dynamics of Oryza sativa L. var. sylvatica . The input variables included in the model were the seedbank composition; the number of panicles per plant and seeds per panicle; the rate of shattering; the seed longevity and the number of weed seeds contained in the sown grain; the type of soil tillage (ploughing, minimum and No tillage); the weed control efficacy; and the predation. The output variables were the number of seedlings that emerged from different depths and the seedbank evolution. The model relies on probability matrices that predict the vertical movement of the seeds after different soil tillage practices. Sensitivity analysis showed that the weed control efficacy and number of grains per panicle were the parameters that had the highest influence on the development of the weed population. The model evaluation was carried out by comparing the predicted with the observed seedling emergence at different seedbank values and under different soil tillage conditions. The model performance showed a tendency to overestimate seedling densities. The agreement between the estimated and experimental data was closely related to the accuracy of the input values of the seed distribution along the soil profile.     

Seed survival and predation of Anoda cristata in soyabean crops

Anoda cristata is a troublesome annual broad-leaved weed in summer crops in the rolling Pampa in Argentina; seeds are the only source of regeneration of this species. Seed persistence or depletion is the result of survival and loss processes, including predation. The objective of this study was to determine survival at two burial depths in undisturbed soil and predation rates of A. cristata seeds in soyabean crops in different rotations and tillage systems. Survival was discontinuous and decreased to 25% after 35 months, after which no further reduction in survival was observed to the end of the experiment at 96 months. No differences in seed survival between seeds placed on the soil surface and buried 5 cm below the soil surface were found at 80 months, but at later times survival was lower for seeds placed on the soil surface. Predation rates ranged between 0.3% day⁻¹ and 6.7% day⁻¹. Of the models tested, a polynomial regression of the rate of predation with time gave the best representation of seed predation. From January to July, predation was higher in non-tillage plots in the wheat/soyabean rotation. There was no significant difference in predation rates between tillage systems in the soyabean monoculture and no difference between planting densities. Higher crop residue levels in non-tillage plots in the wheat/soyabean rotation was the dominant factor influencing seed predation, probably because such habitat favours the presence of seed predators.     

Agronomic practises for weed control in turmeric (Curcuma longa L.)

Weeds are the main problem with turmeric (Curcuma longa L.) cultivation where herbicides are not allowed. This is because herbicides cause water contamination, air pollution, soil microorganism hazards, health hazards, and food risks. Considering turmeric's medicinal value and the environmental problems caused by herbicides, various agronomic practises have been evaluated for non‐chemical weed control in turmeric. One additional weeding is required before turmeric emergence and weed infestation is much higher when turmeric is planted in February and March, as compared to April, May or June planting. A similarly higher yield of turmeric is achieved when it is planted in February, March, and April, compared to late plantings. Weed emergence and interference are not affected by planting depth, seed size, planting pattern, planting space, ridge spacing, and the row number of turmeric until 60 days after planting. This is because turmeric cannot develop a canopy structure until then. Thereafter, weed infestation reduces similarly and significantly when turmeric is planted at depths of 8, 12, and 16 cm, compared to shallower depths. The yield of turmeric at these depths is statistically the same, but the yield for the 16 cm depth is difficult to harvest and it tends to decrease. Turmeric grown from seed rhizomes (daughter rhizomes) weighing 30–40 g reduces weed infestation significantly and obtains a significantly higher yield compared to smaller seeds. The mother rhizome also can suppress weed infestation and increase the yield markedly. Around 9% weed control and 11% higher yield are achieved by planting turmeric in a triangular pattern compared to a quadrate pattern. The lowest weed infestation is found in turmeric grown in a 20 or 30 cm triangular pattern and the highest yield is obtained with the 30 cm triangular pattern. Turmeric gown on two‐row ridges spaced 75 cm apart shows excellent weed control efficiency and obtains the highest yield. This review concludes that turmeric seed rhizomes of 30–40 g and/or the mother rhizome could be planted in a 30 cm triangular pattern at the depth of 8–12 cm on two‐row ridges spaced 75–100 cm apart during March to April in order to reduce weed interference and obtain a higher yield. Mulching also suppresses weed growth and improves the yield. The above agronomic practises could not control weeds completely; biological weed management practises could be integrated in turmeric fields using rabbits, goats, sheep, ducks, cover crops or intercrops.     

Diversity in weed seed production and the soil seed bank: Contrasting responses between two agroecosystems

This study was carried out to compare the diversity in seed production and the soil seed bank in a dryland and an irrigated agroecosystem in the dry tropics. Both agroecosystems showed a comparable number of species, but only 25% and 38% similarity during the winter and rainy cropping seasons, respectively. In the irrigated agroecosystem, the amount of seed production diversity was almost double in the winter season, compared to the rainy season. The weed seedbank diversity was low but was sensitive to cropping practices and seasons in both agroecosystems. A considerably smaller soil seedbank size in the irrigated agroecosystem (cf. dryland) was related to lowered weed seed production. The dryland agroecosystem showed a greater accumulation of the seeds of broad‐leaved weeds, whereas the irrigated agroecosystem accumulated more seeds of the grasses or sedges. About three‐fourths of the seeds during the winter season were accounted for by Anagallis arvensis and Chenopodium album in the dryland agroecosystem and by C. album and Melilotus indica in the irrigated agroecosystem. However, during the rainy season, Ammannia baccifera, Echinochloa colona and Cyperus rotundus dominated in both agroecosystems. The changes in the weed seed bank and its diversity are mainly attributed to differences in water management, which tends to reduce species diversity, especially at a lower depth, but leads to the dominance of some potentially noxious weeds (e.g. Phalaris minor and M. indica). Approximately double the soil seedbank size and a greater diversity at a lower depth might indicate an adaptive mechanism in the storage of weed seeds in the dryland agroecosystem.     

A comparison of techniques for estimation of arable soil seedbanks and their relationship to weed flora

Summary. Post harvest soil samples taken during the autumn of 1985 and 1986 were split and estimates made of the weed seedbank using two methods: (1) a physical separation of seed from the soil mineral fraction by a sieving/flotation procedure and (2) by placing soil in shallow containers in a greenhouse where seeds could germinate and be periodically counted over a period of eight months. Seedbank estimates derived from each procedure were analysed to determine the suitability of each technique for detecting treatment differences from an experiment evaluating tillage/herbicide effects on weed populations. Both techniques were suitable for determination of seedbank changes due to different tillage treatments and herbicide inputs. The two techniques also proved effective for detection of individual species in the seedbank and the two techniques provided comparable estimates of the relative density of individual weed species in the seedbank. Weed seedbank estimates obtained by the physical extraction procedure from the autumn 1985 soil samples were correlated with weed seedling counts made in the spring of 1986. In most cases, weed seedlings represented less than 10% of the number of seeds estimated by physical extraction the preceding autumn. Individual species seed estimates and subsequent weed counts were poorly correlated which indicated that the seed count estimates alone were poor predictors of weed flora.     

Potential of weed seedbanks for managing weeds: a review of recent New Zealand research

Weed seedbanks are the primary source of weeds in cultivated soils. Some knowledge of the weed seedbank may therefore be appropriate for integrated weed management programs. It would also be very useful in planning herbicide programs and reducing the total herbicide use. However, a number of problems are inherent in the estimation of the seedbank size for arable weeds that usually have annual life cycles. In a long-term research project we have investigated the dynamics of weed seedbanks in corn fields for the past 8 years. Specific studies have included (i) developing cheap and efficient methods for estimating the weed seedbank; (ii) developing guidelines for efficient soil sampling (including the number and size of samples); (iii) influence of cultivation methods on weed seed distribution; (iv) mapping the spatial variability of the seedbank; (v) estimating the rate of seedbank decline for certain weed species; and (vi) assessing the potential of using the weed seed content in the soil to predict future weed problems. This paper reviews and summarizes the results of our research on the above aspects. The strong correlation between seedlings emerged in the greenhouse and seeds extracted in the laboratory for the most abundant weed species has demonstrated the potential for using the weed seed content of the soil to predict future weed infestations. The next step is to establish correlations with field emergence under commercial conditions using the sampling guidelines developed in our studies. Subsequently, we aim to offer the weed seedbank estimation as a commercial service to farmers for planning the most appropriate weed management options.     

Impact of cropping systems on the weed seed banks in the northern Great Plains, USA

Very little research has been done on weed seedbank communities in the northern Great Plains region of the USA. The objectives of this study were to evaluate the effects of management systems on the weed seed banks and to assess the relationship between the weed seed banks and the above-ground weed communities. The seed banks were sampled along a range of areas of above-ground weed diversity in organic and conventional spring wheat production fields near Big Sandy, Montana, over 2 years. Eight 1 m × 0.33 m areas were selected in each field to encompass a wide range of above-ground weed diversity and soil cores were taken in each area to a depth of 20 cm and split in half at 10 cm. The number of seeds recovered from the top 10 cm of soil and the 10–20 cm depth were significantly affected by the sampling year and an interaction between the cropping system and the sampling year. The year was the only significant predictor affecting the weed seedbank diversity at both depths. A significant interaction between the management system and the year observed at the 10–20 cm sampling depth reflected the higher rate of decrease in diversity occurring between 2005 and 2006 in the conventionally managed fields compared with the organic fields. A multivariate ordination indicated that, although the year played a significant role in determining the weed seedbank communities, the management system had a role only during 2006. We failed to detect strong correlations between the above-ground and underground weed communities. The results of this study suggest that, in the studied region, yearly fluctuations in environmental factors have significant impacts on the weed seed banks.     

Application method of nitrogen fertilizer affects weed growth and competition with winter wheat

The management of crop fertilization may be an important component of integrated weed management systems. A field study was conducted to determine the effect of various application methods of nitrogen (N) fertilizer on weed growth and winter wheat yield in a zero-tillage production system. Nitrogen fertilizer was applied at 50 kg ha⁻¹ at the time of planting winter wheat over four consecutive years to determine the annual and cumulative effects. The nitrogen treatments consisted of granular ammonium nitrate applied broadcast on the soil surface, banded 10 cm deep between every crop row, banded 10 cm deep between every second crop row, and point-injected liquid ammonium nitrate placed between every second crop row at 20 cm intervals and 10 cm depth. An unfertilized control was also included. Density, shoot N concentration and the biomass of weeds was often lower with subsurface banded or point-injected N than with broadcast N. The winter wheat density was similar with all N fertilizer application methods but wheat shoot N concentration and yield were consistently higher with banded or point-injected N compared with broadcast N. In several instances, the surface broadcast N did not increase the weed-infested wheat yield above that of the unfertilized control, indicating that it was the least preferred N application method. Depending on the weed species, the weed seedbank at the conclusion of the 4 year study was reduced by 29–62% with point-injected N compared with broadcast N. Information gained from this study will be used to develop more integrated weed management programs for winter wheat.