The Northern Great Plains of the United States is a major production region for organic pulse crops that are prone to yield losses due to weeds. Weed management in organic systems relies on the integration of several tactics to stack additive effects and for redundancy to deal with variable efficacy of individual weed management practices. To address the need for effective, integrated weed management, we conducted a 2-yr trial that evaluated the effects of planting date, seeding rate, and preemergent weed control practices (shallow tillage and flame weeding) on weed biomass, crop density, and yield in organically managed chickpea (Cicer arietinum L.) in Montana. Stacking weed management practices increased yields. Early planting had the largest effects on yields, increasing them by 1.8- to 3.6-fold compared with planting 10 to 14 d later. Increasing the seeding rate from the standard rate (43 viable seeds m−2) by 50% increased yields by 47% from 889 to 1,304 kg ha−1. Both preemergent weed control practices increased yields by 40% to 50 % relative to the non-weeded controls. By integrating all three practices, yields of organic chickpea increased greater than 6-fold from 318 kg ha−1 in the controls to 2,006 kg ha−1. The effects of weed control treatments on midseason weed biomass were complex and variable. Although efficacy of the cultural (seeding rate and planting date) and physical (preemergent) treatments on weed biomass varied between years and when combined with other treatments, their full integration, that is, early planted, at higher seeding rate, and preemergent weed control, produced consistently lower weed biomass (84% reduction on average) compared with the standard grower practice (later planting, standard seeding rate, no preemergent weed control). The results lend support to the concept of integrating multiple weed management practices to achieve weed control and high yields in organically managed crops.

In Oklahoma, downy brome and cheat are difficult-to-control winter annual grasses. In the past, cheat infested most of the winter wheat hectares harvested in Oklahoma. Biotypes that are cross-resistant to acetolactate synthase–inhibiting herbicides have left growers with minimal management options for conventional and herbicide-tolerant systems. Field trials near Lahoma, Oklahoma, in 2019–2020 and 2020–2021 evaluated integrated management of cheat and downy brome using three strategies: planting date (optimal, delayed, and late), cultivar selection (high and low competitiveness), and herbicide choice (no herbicide, sulfosulfuron at 35.2 g ai ha−1 and pyroxsulam at 18.4 g ai ha−1). Visual control, weed species present, wheat biomass at heading, and grain yield data were collected. In 2019–2020, 8 to 9 wk after treatment, visual control increased by 15% with the delayed planting compared with the optimal planting date and 14% with the late planting date. In 2020–2021, similar control (∼99%) was recorded for delayed and late plantings with 23% greater control than the optimal timing. Due to a lack of weed coverage, weed biomass in 2019–2020 had no response to planting date, cultivar, or herbicide treatment. Downy brome biomass during 2020–2021 was approximately 90% lower with delayed to late planting dates than the optimal planting date. In the same year, downy brome and cheat biomass were low (≤0.4 and 0.2 g m−2) and 98% less after an herbicide application than a nontreated area. Wheat grain yield at the optimal planting date was greater than yields from delayed and late plantings in 2019–2020. A delay in planting from the optimal date to delayed or late timings decreased wheat yield by 14% and 21%, respectively. In 2020–2021, wheat yield from the late planting was reduced by 57% compared with the optimal planting yield. Delaying the planting date and the use of a common herbicide can suppress cheat and downy brome, but a decline in wheat yield may occur.

Weed interference is a major factor that reduces peanut (Arachis hypogaea L.) yield in the United States. Peanut growers rely heavily on herbicides for weed control. Although effective, herbicides are not a complete solution to the complex challenge that weeds present. Therefore, the use of nonchemical weed management options is essential. The literature on weed research in peanut in the past 53 yr in the United States was reviewed to assess the achievements and identify current research gaps and prospects for nonchemical weed management for future research. More than half (79%) of the published studies were from the southeastern United States. Most studies (88%) focused on weed management, while fewer studies (12%) addressed weed distribution, ecology, and competitive mechanisms. Broadleaf weeds were the most frequently studied weed species (60%), whereas only 23% and 19% of the published studies were relevant to grasses and Cyperus spp., respectively. Seventy-two percent of the published studies focused on curative measures using herbicides. Nonchemical methods using mechanical (5%) and preventive (13%) measures that influence crop competition and reduce the buildup of the weed seedbank, seedling recruitment, and weed seed production have received less attention. In most studies, the preventive weed management measures provided weed suppression and reduced weed competition but were not effective enough to reduce the need for herbicides to protect peanut yield. Therefore, future research should focus on developing integrated weed management strategies based on multiple preventive measures rather than one preventive measure combined with one or more curative measures. We recommend that research on mechanical weed management should focus on the role of cultivation when integrated with currently available herbicides. For successful weed management with lasting outcomes, the dominant weed communities of specific target locations should be addressed within the context of climate change and emerging constraints rather than focusing on single problematic species.

Junglerice [Echinochloa colona (L.) Link.] is the most important grass weed species in Australian summer cropping systems. Although it is mainly a spring- and summer-emerging weed species, field observations suggest that E. colona is expanding its seasonality. A common garden experiment was conducted at the University of Queensland farm to examine the effect of planting dates on phenology, growth, and fecundity of eight populations of E. colona. All populations were planted every second month from September to July in 2019 to 2020 and 2020 to 2021. Echinochloa colona took the shortest time (4 to 6 d) to emerge when planted in November or January. However, the November population took the longest number of growing degree days to exhibit panicle emergence. In both years, populations differed in height and leaf, tiller, panicle, and seed production in response to planting times. Plants produced significantly greater biomass for the November planting (123 to 147 g plant−1) followed by the January planting and then the September planting. The March planting produced the lowest biomass. In the first year, the lowest number of seeds (3,500 seeds plant−1) was produced by the March planting; however, in the second year, similar numbers of seeds were produced by the March and July plantings. In the first year, seed production (51,000 seeds plant−1) was greatest for the November planting; however, some populations also produced a similar number of seeds for the January planting. In the second year, significantly greater seed production (111,000 seeds plant−1) was observed for the January planting compared with other planting dates. The aboveground biomass and seed production of E. colona were positively correlated. This study reveals variations among E. colona populations and suggests that although greater emphasis must be placed on controlling spring- and summer-emerging plants, management practices need to be extended throughout the year to control E. colona in southeastern Australia.

The role of weed suppression by the cultivated crop is often overlooked in annual row cropping systems. Agronomic practices such as planting time, row spacing, tillage and herbicide selection may influence the time of crop canopy closure. The objective of this research was to evaluate the influence of the aforementioned agronomic practices and their interaction with the adoption of an effective preemergence (PRE) soil residual herbicide program on soybean canopy closure and yield. A field experiment was conducted in 2019 and 2020 in Arlington, WI, as a 2×2×2×2 factorial in a randomized complete block design, including early (late April) and standard (late May) planting time, narrow (38 cm) and wide (76 cm) row spacing, conventional tillage and no-till, and soil-applied PRE herbicide (yes and no; flumioxazin 150 g ai ha−1 + metribuzin 449 g ai ha−1 + pyroxasulfone 190 g ai ha−1). All plots were maintained weed-free throughout the growing season. In both years, early planted soybeans reached 90% green canopy cover (T90) before (7 to 9 d difference) and yielded more (188 to 902 kg ha−1 difference) than the standard planted soybeans. Narrow-row soybeans reached T90 earlier than wide-row soybeans (4 to 7 d difference), but yield was similar between row spacing treatments. Conventional tillage resulted in a higher yield compared to a no-till system (377 kg ha−1 difference). The PRE herbicide slightly delayed T90 (4 d or less) but had no impact on yield. All practices investigated herein influenced the time of soybean canopy closure but only planting time and tillage impacted yield. Planting soybeans earlier and reducing their row spacing expedites the time to canopy closure. The potential delay in canopy development and yield loss if soybeans are allowed to compete with weeds early in the season would likely outweigh the slight delay in canopy development by an effective PRE herbicide.

Organic crop production is often limited by the inability to control weeds. An 18-yr data set of weed cover in organic crop rotations at the long-term Farming Systems Project at Beltsville, MD, was analyzed to identify meteorological and management factors influencing weed abundance. A path analysis using structural equation models was employed to distinguish between the direct effect of factors on weed cover and the indirect effect on weed cover through effects on crop competitiveness. Grain yield of corn (Zea mays L.) and soybean [Glycine max (L.) Merr.] served as a surrogate for crop competitiveness and was found to be the most important factor influencing weed cover. Precipitation during late vegetative and early reproductive crop growth had a strong positive effect on crop yield, and thereby a negative indirect effect on weed cover, but this effect was partially offset by a positive direct effect on weed cover. Delayed crop planting date and crop rotational diversification including crops other than summer row crops had a moderate negative effect on weed cover, while having minimal effect on crop performance. Rotary hoeing also had a direct negative effect on weed cover, but a corresponding negative effect on crop performance resulted in a diminished total effect on weeds. Results demonstrate the complex interactions that define the relative abundance of weeds faced by organic growers, but, generally, factors that enhanced crop competitiveness provided the most effective weed management.

The influence of relative planting date on the growth of common cocklebur (Xanthium pensylvanicum Wallr. ♯ XANST), common ragweed (Ambrosia artemesiifolia L. ♯ AMBEL), sicklepod (Cassia obtusifolia L. ♯ CASOB), and redroot pigweed (Amaranthus retroflexus L. ♯ AMARE) grown in competition with soybean [Glycine max (L.) Merr. ‘Bragg’] was studied in the greenhouse. Increases in dry matter and height were slower for the five weed species than for soybean throughout the period of the study. The root: shoot ratio of soybean was the highest of any plant in the study, while common ragweed, common cocklebur, common lambsquarters, and sicklepod were intermediate, and redroot pigweed was the lowest. Soybean dry weight was always reduced when grown in competition with a weed. Soybean dry-matter production was reduced most when weeds were planted 2 weeks before soybean, especially with common cocklebur and common lambsquarters. Weed dry-matter content was severely reduced when the weed seed were planted simultaneously with or following soybean. Soybean height was usually reduced by competition with the weeds. The height of common ragweed was increased, however, when planted simultaneously with soybean. Common lambsquarters, redroot pigweed, and common ragweed heights were increased when planted 2 weeks prior to soybean.

The ability of honeyvine milkweed [Ampelamus albidus (Nutt.) Britt.] to establish and develop from seed was studied in laboratory and field experiments. Optimum germination temperature was 30 C. Seed incubated at cooler temperatures and then transferred to 30 C germinated equally as well as seed incubated continually at 30 C. Germination was unaffected at moisture stress levels between 0 and −4.6 bars, but was decreased at levels between −4.6 and −12.8 bars. The optimum pH range for germination was between 5 and 7. The greatest emergence of seedlings occurred at a depth of 0.5 cm with no emergence occurring at depths greater than 5 cm. Greater emergence was obtained with a loam than sandy loam at all planting depths except 0.5 cm. Field plots seeded on May 1 gave maximum seed production. Seed production decreased with each 2-week delay in planting. Planting dates of July 10 or later produced no seed. Seed germination was affected little by delayed planting. The following spring, regrowth from plants seeded on June 12 or later was less vigorous than regrowth from plants seeded earlier.

Fall-planted longspine sandbur began to emerge in April, peaked in late April or May, and continued at low levels through October. During the first year after seeding, 98% of the total seedlings emerged prior to June. Fall-planted puncturevine began to emerge in late April or May and continued through October. Puncturevine emergence was multipeaked and 75% of each season's total emerged prior to mid-July. A similar number of puncturevine seedlings emerged the second and third years after planting as in the first. The emergence pattern for a species was similar each year regardless of how long the seed had lain in the soil. Longspine sandbur required 7 to 13 weeks from emergence to heading and produced approximately 2600, 1300, 180, and 3 spikes per plant when planted in May, June, July, and August, respectively. Puncturevine flowered within 3 to 4 weeks after emergence when temperatures were favorable and produced an average of 5600, 5200, 3600, and 200 burs per plant when planted in May, June, July, and August, respectively.

Controlled – environment studies were conducted to determine the influence of temperature, light, seed weight, depth of planting, substrate pH, and salinity on the germination and emergence of silverleaf nightshade (Solanum elaeagnifolium Cav.). The effects of planting date, top removal, and root-cutting length on establishment were studied in the field. Fluctuating temperatures of 20 to 30C produced 57% germination. Maximum germination, 59%, occurred between pH 6 and 7. NaCl concentrations greater than 2500 ppmw caused germination to decrease 85% or more compared to the control. Light was not important for germination. Mean seedling emergence was 46% from depths of 1.0 to 2.5 cm. Silverleaf nightshade seedling emergence from a 2-cm depth was 31% greater in a sandy soil than a loam. Delayed seeding caused a decline in dry-weight accumulation of above-ground parts. Fifteen percent of seedlings clipped 15 days after emergence were capable of regrowth, and after 30 days or more, 90% of the clipped plants regrew.

Field studies evaluated the effects of crop, crop rotation, planting date, row spacing, no-till planting, and herbicides on wild-proso millet control. Benefin and EPTC reduced wild-proso millet biomass in new seedings of alfalfa, and the combination of herbicides and forage harvest prevented wild-proso millet seed production in that crop. Wild-proso millet seedling populations were reduced and corn yields increased when corn followed 1 to 4 yr of alfalfa. Apparent effectiveness of herbicides in corn increased after cropping with alfalfa. Germination of buried wild-proso millet seed decreased approximately 90% after 54 months which is equivalent to 4-yr prior cropping to alfalfa. Wild-proso millet control and field and sweet corn yields increased when the crops were planted late season (May 17) rather than early season (April 27). Planting sweet corn in rows spaced 76 cm rather than 108 cm apart also increased sweet corn yields. EPTC plus dichlormid (EPTC+) plus cyanazine always controlled wild-proso millet equal to or better than EPTC+ alone. When field corn was planted no-till into killed alfalfa sod, combinations of pendimethalin plus simazine and pendimethalin plus cyanazine provided the best wild-proso millet control and corn yields. But the following year when corn was no-till planted into corn stubble of the identical plots, wild-proso millet control from the same treatments tended to be lower and corn yields were reduced.

Interseeding annual clovers in cereal grains may help organic producers reduce use of tillage following cereal harvest. Using clovers that winterkill would minimize need for tillage in the spring also. The objective of this study was to evaluate seedling emergence and survival of berseem clover (Trifolium alexandrinum L.) in winter wheat (Triticum aestivum L.). Berseem clover (hereafter, referred to as berseem) was planted 0, 2 and 4 weeks after initiation of winter wheat growth in the spring. Berseem density was highest when planted on April 12, 2 weeks after winter wheat broke dormancy. Establishment density was 40–80% less with the other planting dates. A dry interval during the 5 weeks preceding winter wheat harvest reduced seedling survival of berseem, killing more than 80% of seedlings. Winter wheat yield was reduced at the last planting date of berseem, which was attributed to mechanical injury to winter wheat by the drill when planting berseem. Berseem may not be viable for interseeding at this location or in drier regions. Clover species that are more drought tolerant will be needed.

Cultivated rice yield losses due to red rice infestation vary by cultivar, red rice density, and duration of interference. The competition effects of red rice could be influenced further by emergence characteristics, red rice biotype, and planting time of cultivated rice. We aimed to characterize the emergence of red rice biotypes at different planting dates and evaluate the effect of red rice biotype, rice cultivar, and planting date on cultivated rice yield loss. Field experiments were conducted at the Southeast Research and Extension Center, Rohwer, AR, and at the Arkansas Rice Research and Extension Center, Stuttgart, AR, in the summer of 2005 and 2006. The experimental design was a split-split plot with three or four replications. Planting time, ClearfieldTM (CL) rice cultivar, and red rice biotype were the main plot, subplot, and sub-subplot factors, respectively. There were three planting times from mid-April to mid-May at 2-wk intervals. CL rice cultivars, CL161 and hybrid CLXL8, and 12 red rice biotypes were planted. The emergence rate and coefficient of uniformity of germination differed among some red rice biotypes within a planting time. Planting date affected the emergence characteristics of red rice biotypes. The mean emergence rate of red rice was 0.043 d−1 in the mid-April planting and 0.058 d−1 in the late April planting. For the mid-April planting, 50% of red rice biotypes emerged in 20 ± 2 d compared with 15 ± 2 d for CL rice cultivars. Yield losses due to red rice biotypes generally increased in later planting dates, up to 49%. Yield losses due to interference from red rice biotypes ranged from 14 to 45% and 6 to 35% in CL161 and CLXL8, respectively. Cultivated rice became less competitive with red rice in later plantings, resulting in higher yield losses.

Grower adoption of no-tillage (NT) approaches to organic soybean production has been limited, in part because of the perceived risks of ineffective cover crop management and lack of season-long weed suppression. We conducted research in 2008 and 2009 to assess those risks by quantifying the effects of winter rye cover-crop management (tilling, crimping, or mowing), soybean planting date (mid May or early June), and row width (19 or 76 cm) on weed recruitment, emergence patterns, season-long suppression, and late-season weed community composition in transitional organic production systems. The weed plant community consisted largely of summer annual species in each year, with velvetleaf or common lambsquarters as the most abundant species. Seedling recruitment from the soil seedbank varied between years, but velvetleaf recruitment was consistently greater in the tilled rye than in the NT rye treatments. Weed emergence tended to peak early in the season in the tilled rye treatment, but in the NT rye treatments, the peak occurred in mid or late season. More-diverse summer annual and perennial species were associated with the NT rye treatments. Even so, weed suppression (as measured by late-season weed shoot mass) was much greater in crimped or mowed rye NT treatments than it was in the tilled treatment. Weed suppression among NT rye treatments was greater in 19- than in 76-row spacing treatments in each year and was greater for mid May than it was for early June planted soybean in 2009. The NT planting of soybean into standing rye before termination (crimping or mowing) facilitated timely planting of soybean, as well as effective, season-long weed suppression, suggesting that those approaches to rye and weed management are of less risk than those typically perceived by growers. Our results suggest that NT systems in winter rye provide effective weed-management alternatives to the typical tillage-intensive approach for organic soybean production.

Benghal dayflower (formerly known as tropical spiderwort) is one of the most troublesome weeds in Georgia cotton. Field studies were conducted from 2003 to 2005 to evaluate the relationship between the duration of Benghal dayflower interference and cotton yield to establish optimum weed-control timing. To determine the critical period of weed control (CPWC), Benghal dayflower interference with cotton was allowed or prohibited in 2-wk intervals between 0 to 12 wk after crop planting. Maximum yield loss from Benghal dayflower in May-planted cotton was 21 to 30% in 2004 and 2005, whereas cotton planting delayed until June resulted in maximum yield losses of 40 to 60%. June-planted cotton had a CPWC of 190 to 800 growing degree days (GDD) in 2004 (52-d interval beginning at 16 d after planting [DAP]) and 190 to 910 GDD in 2005 (59-d interval beginning at 18 DAP). In contrast, May-planted cotton in 2005 had a narrower CPWC interval of 396 to 587 GDD (18 d) that occurred 3 wk later in the growing season (initiated at 39 DAP). May-planted cotton in 2004 did not have a critical range of weed-free conditions. Instead, a single weed removal at 490 GDD (44 DAP) averted a yield loss greater than 5%. It is recommended that fields infested with Benghal dayflower be planted with cotton early in the growing season to minimize weed interference with the crop.

Sweet corn is planted over a long season to temporally extend the perishable supply of ears for fresh and processing markets. Most growers' fields have weeds persisting to harvest (hereafter called residual weeds), and evidence suggests the crop's ability to endure competitive stress from residual weeds (i.e., crop tolerance) is not constant over the planting season. Field studies were conducted to characterize changes in the residual weed community over the long planting season and determine the extent to which planting date influences crop tolerance to weed interference in growth and yield traits. Total weed density at harvest was similar across five planting dates from mid-April to early-July; however, some changes in composition of species common to the midwestern United States were observed. Production of viable weed seed within the relatively short growth period of individual sweet corn plantings showed weed seedbank additions are influenced by species and planting date. Crop tolerances in growth and yield were variable in the mid-April and both May plantings, and the crop was least affected by weed interference in the mid-June and early-July planting dates. As the planting season progressed from late-May to early-July, sweet corn accounted for a great proportion of the total crop–weed biomass. Based on results from Illinois, a risk management perspective to weeds should recognize the significance of planting date on sweet corn competitive ability. This work suggests risk of yield loss from weed control failure is lower in late-season sweet corn plantings (June and July) than earlier plantings (April and May).

In the northern Great Plains, fields are land rolled after the planting of annual pulse and forage crops to push rocks back into the soil to prevent damage to harvest equipment. Field trials were conducted in 2004 and 2005 to determine if land rolling influenced weed density or biomass associated with field pea, forage barley, and summer fallow. The experiment included two planting dates, conventional and delayed, for both barley and pea. Separate fallow plots were included with each planting date. Preplant tillage was conducted with a field cultivator for all treatments. Across years, crops, and planting dates, land rolling approximately doubled densities of tumble mustard, Russian thistle, kochia, and redroot pigweed shortly after crop emergence and at harvest compared with nonrolled. Land rolling increased density of early-emerging green foxtail but density at harvest was not affected. Wild oat densities were not influenced by rolling. Weed biomass at harvest was greater after land rolling than nonrolled. Land rolling after planting decreased subsequent pea yield by 330 kg/ha, but did not influence water use or water use efficiency. Land rolling is advantageous by hastening depletion of soil broadleaf weed seed banks in forage barley, but may increase problematic broadleaf weeds in pea.

A study was conducted in 1995 and 1996 to determine the effect of soybean planting date, tillage level, and glyphosate application on sicklepod control and seed production. Soybean was planted in April, May, June, and July into conventional and no-till seedbeds. Herbicide programs evaluated were metribuzin plus chlorimuron preemergence (PRE) followed by (fb) chlorimuron postemergence (POST) (standard program [STD]), metribuzin plus chlorimuron PRE fb glyphosate POST as-needed, and glyphosate POST as-needed. Control was similar across planting dates in both years with slight variations due to weather. The July planting date had the lowest total sicklepod seed production over the 2-yr study. Sicklepod control was better in conventional tillage, but soybean yields were greater in no-till. Herbicide programs that included glyphosate provided greater sicklepod control, lower sicklepod seed production, and higher soybean yields than the STD. Use of glyphosate in combination with later planting dates, especially July, has the potential to prevent sicklepod seed accumulation in the soil while maintaining yields in a dryland soybean production system.

Stem and cob borers cause substantial damage to maize and affect the quality and economic value of maize in West Africa. Manipulation of planting dates is considered a possible mechanism for averting the overall impact of borers and their damage to the crop. Experiments were carried out in southern Benin to evaluate the effect of various planting dates on the incidence and damage to maize by Sesamia calamistis (Hampson). The trials were conducted at the Benin station of the International Institute of Tropical Agriculture (IITA) at Abomey-Calavi and at Sèhouè, located 70 km north of the IITA, Benin station. The planting dates were: early planting (the day following the first rains), intermediate planting (2–3 weeks after the early planting) and late planting (4–5 weeks after the early planting). The experiments were carried out in the main and minor cropping seasons, respectively, during two successive years in 2003 and 2004. The variables measured included population density of S. calamistis, percentage of infested plants and cob damage. In the main cropping season, incidence of stemborers and percentage of infested plants were higher in the late planting than in the early planting and intermediate planting treatments. The manipulation of planting dates for the control of S. calamistis during the minor maize growing season is not recommended.

Introduction. Planting time is considered as one of the most important factors for successful strawberry cultivation. Traditionally, under north-Indian plains, strawberry is planted after the second week of October, which results in the availability of fruits for a month or so. With the use of plasticulture techniques, the planting time can be enhanced, which facilitates early and higher production, and enhances availability of the fruit for a longer period. Mulching is the most important cultural practice in strawberry, which influences plant growth, fruit yield and quality. Hence, studies were conducted to determine the influence of planting time and mulching on growth, flowering and fruiting behaviour, yield and quality of strawberry in northern plains of India. Materials and methods. Studies were conducted on ‘Chandler’ strawberry with three planting times (mid-September, mid-October and mid-November) as the main effect and three mulching materials (black polyethylene, clear polyethylene and paddy straw) as the sub-main effect in a split-plot design with three replications. Standard procedures were adopted for making observations on plant growth parameters, flowering and fruiting behaviour, yield and quality parameters under different treatment combinations. Results and discussion. Mid-September planting favoured vigorous growth, enhanced flowering and fruiting, which resulted in the production of the largest fruits and highest yield of the best quality. Among the three different mulch materials, plants mulched with black polyethylene had the best growth, fruit weight, yield and quality compared with those mulched with clear polyethylene or paddy straw mulch. The [planting time × mulching] interaction was also found to be significant for all measured parameters. Conclusion. Our study revealed that, in northern plains of India, to get an early and high yield of the best quality under a micro-irrigation system, Chandler strawberry could be planted in mid-September if mulched with black polyethylene.