The development of sustainable farming systems depends on our ability to predict and manage the response of weed communities to changes in cropping practices. A study was established at Normandin, Québec, Canada, to investigate the influence of liquid dairy manure and mineral fertilizer, as well as chisel and moldboard plow tillage systems, in a spring barley monoculture and a 3-yr spring barley-forage rotation that included red clover and timothy. Weed species richness (Margalef's DMG), evenness (Shannon's E), and diversity (Shannon's H') were examined in these treatments from 1992 to 1995. Nutrient source had no effect on any of the three diversity indices. Evenness values were extremely low in all years, suggesting dominance of a few weed species in most treatments. Weed species richness and diversity generally were greater in the barley-forage rotation compared with the monoculture. Tillage effects on richness and diversity varied with crop rotation. Margalef's DMG and Shannon's H' were greater in 1993 and 1995, but they were lower in 1994 when chisel was compared with moldboard plowing in the monoculture. In 1994, chickweed density was about five times greater in the chisel-plowed monoculture compared with other treatment combinations of rotation and tillage. In 1995, only one species with a density of six plants m−2 occurred in the moldboard-plowed monoculture compared with three to six species and densities of 51 to 832 plants m−2 in the other rotation by tillage treatments. Climatic conditions and herbicide use patterns in the different crop rotation treatments may have contributed to the more dynamic nature of weed species diversity in the barley monoculture. Reduced frequency of tillage and herbicide application; management of the forage stands, especially with regard to their termination; and improved soil resource availability likely explained the increased but more stable diversity of the weed communities in the barley-forage rotation.

Weed management decisions based on weed threshold models offer the opportunity to reduce herbicide use by allowing the possibility of forgoing treatment or lowering rates. Weed thresholds based on a relative leaf-cover model were tested during a 4-yr period at two locations. Two 1.62-ha fields, planted to conventional and glyphosate-resistant corn (2004, 2005, 2007) or soybean (2006), were divided in 900 m2 sections. Herbicides were applied postemergence to each of these sections with either variable rates based on weed thresholds, or constant full rates. Variable herbicide rates included: no application, half rate, or full rate. Relative weed cover values of 0.2 and 0.4 (corn) or 0.1 and 0.3 (soybean) served as thresholds for incremental rates. Digital images were used to evaluate the relative weed cover. Weed density was assessed before and after herbicide application. Weed seed production was estimated for two species in 2004 and 2005. No difference in crop yield, relative weed cover, weed density, or weed seed production was observed between conventional and glyphosate-resistant cropping systems. During the first year, herbicide use reduction was obtained (−85.4%) with marginal crop yield loss (5 to 15%). In the subsequent 3 yr, preherbicide weed densities increased and concomitant increases in relative weed cover values did not allow more than a 10% overall reduction in herbicide use. This threshold model designed to maintain crop yields within a given year did not allow significant reduction in herbicide use during the following 3 yr. Residual weed populations most likely replenished the seed bank to levels that allowed weed densities to increase afterward. Increased weed density over time in plots treated with full rates of herbicide every year also indicated that a single postemergence herbicide treatment was not sufficient to contain weed populations at low levels every year in this corn–soybean rotation.

The presence of volunteer canola is becoming a significant agro-ecological concern, given the large-scale use of herbicide-tolerant varieties in some areas. Our goal was to estimate the frequency and persistence of volunteer canola in Québec cropping systems by surveying fields that included a single canola crop since 1995. A survey was conducted in 131 fields in the main canola-growing areas of Québec: in the Saguenay-Lac Saint-Jean region and the Québec City–La Pocatière area. Volunteer canola plants were counted in 0.25-m2 quadrats every 10 m along a W pattern, and every 15 m along the margins of 88 fields. Volunteer canola plants were found in 90% of the fields surveyed and in a wide range of crops, including cereal, corn, and soybean. Average densities of 4.9 and 3.9 plants/m2 were found 1 yr after canola production in fields and field margins, respectively. Volunteer canola densities decreased significantly over time. However, volunteer plants were still present at low densities 4 and 5 yr after production. Dense stands of volunteer canola were found before postemergence herbicide application in no-till fields (9.8 ± 4.1 plants/m2), suggesting that, contrary to what was suggested in the literature, seeds could become dormant in no-till as well as in tilled systems. A small proportion of the volunteer canola plants observed in no-till fields near Québec City and Ottawa included plants that had overwintered, either originating from fall-germinated seedlings, harvested adult plants that had grown new leaves before the onset of winter, or spring regrowth from the base of unharvested adult plants from experimental plots. The presence and persistence of low densities of volunteer canola may not have been a cause of concern until now. However, producers should be made more aware of the potential short-and long-term problems associated with potential gene flow between different herbicide-tolerant canola (HT canola) varieties and also between HT canola and related weed species.

Since 1995, canola cultivars with herbicide resistance (HR) have been readily adopted by Canadian producers. Gene flow between these cultivars with different HR traits has led to the occurrence of double herbicide–resistant (2HR) volunteers. To evaluate the fitness of canola volunteers with double HR, we compared three 2HR combinations to each of their parent single-HR plants (1HR: glufosinate-R, imidazolinone-R, glyphosate-R) commercial canola lines in separate greenhouse experiments. The replacement series design included five ratios of 2HR vs. 1HR plants at a single density of 129 plants m−2 and three stress treatments: herbicide application with either glufosinate, imazethapyr, or glyphosate; competition with a wheat crop; and a control without herbicide or wheat competition. Fitness indicators included aboveground biomass at 5 and 12 to 16 wk, seed production, and reproductive allocation. The 2HR plants showed delayed reproductive growth but were generally as competitive as 1HR commercial lines. Plant biomass of 2HR canola was comparable to or greater than 1HR canola, whereas seed biomass of 2HR canola was less than that of 1HR canola in half of the cases, likely because of delayed reproductive growth and early harvesting. Glufosinate–glyphosate 2HR was the fittest combination. Herbicide application had little effect on 2HR biomass at harvest, except for imazethapyr, which reduced the biomass and seed production of 2HR plants with imidazolinone-glyphosate resistance by 30%. The latter effect could have been from the unsuspected presence of 2HR plants with only one of the two acetolactate synthase mutations conferring resistance to imidazolinones. Wheat competition reduced fitness values of both 2HR and 1HR canola similarly, but seed production was still 64% that of the controls. Overall, there was little indication of reduced fitness in 2HR canola compared with commercial 1HR varieties.

Phenoxy herbicides are frequently used to control volunteer canola populations. However, there have been claims that poor control could be due to cold acclimation of canola plants in the spring. The objective of this study was to determine whether cold acclimation or growth stage affected the response of canola volunteers to herbicides. In a growth room experiment, canola plants were prehardened and cold acclimated or were grown at 20/12 C and treated with one of six 2,4-D doses. Cold acclimation as achieved by this experiment affected upper and lower asymptotes of the dose–response curve but not the herbicide dose required to reduce canola weight by 50% relative to the nontreated control (GR50), indicating limited cold-related effects on canola tolerance to 2,4-D. Field experiments, conducted in the provinces of Québec and Saskatchewan, examined the effects of canola growth stage on the efficacy of 2,4-D, MCPA, and carfentrazone. Comparisons of the estimates from the dose–response curves confirmed that herbicide efficacy was consistently greater when canola plants were treated at an early growth stage, regardless of cultivar or herbicide used. The GR50 estimates for canola plants treated at a later growth stage exceeded the recommended rates. Some canola plants grown as volunteers in a wheat crop survived 2,4-D or MCPA treatments at 0.5× and 1× rates and produced up to 148 seeds/m2. Efficient control of canola volunteers will be obtained when plants are sprayed at an early growth stage, but near-total control will be highly desirable in order to restrict seedbank buildup, particularly when dealing with canola cultivars with different herbicide-resistant traits.

Many conditions need to be satisfied for gene flow to occur between a transgenic crop and its weedy relatives. Flowering overlap is one essential requirement for hybrid formation. Hybridization can occur between canola and its wild relative, wild radish. We studied the effects of wild radish plant density and date of emergence, canola (glyphosate resistant) planting dates, presence of other weeds, and presence of a wheat crop on the synchrony of flowering between wild radish and canola (as a crop and volunteer). Four field experiments were conducted from 2000 to 2002 in St-David de Lévis, Québec. Flowering periods of wild radish emerging after glyphosate application overlapped with early-, intermediate-, and late-seeded canola 14, 26, and 55%, respectively, of the total flowering time. Flowering periods of early-emerging wild radish and canola volunteers in uncropped treatments overlapped from mid-June until the end of July, ranging from 26 to 81% of the total flowering time. Flowering periods of wild radish and canola volunteers emerging synchronously on May 30 or June 5 as weeds in wheat overlapped 88 and 42%, respectively, of their total flowering time. For later emergence dates, few flowers or seeds were produced by both species because of wheat competition. Wild radish density in canola and wild radish and canola volunteer densities in wheat did not affect the mean flowering dates of wild radish or canola. Increasing wild radish density in uncropped plots (pure or weedy stands) hastened wild radish flowering. Our results show that if hybridization is to happen, it will be most likely with uncontrolled early-emerging weeds in crops or on roadsides, field margins, and uncultivated areas, stressing the need to control the early flush of weeds, weedy relatives, and crop volunteers in noncrop areas.

In July 1996, major floods destroyed several houses occupied by pre-retirees (ages 50–59) and retirees (ages 60 and over). Faced with the task of relocating and rebuilding a new home, several of those older adults lived through difficult post-traumatic adaptation periods. The data collected during in-depth interviews with 31 aging people clearly show that the biopsychosocial health of pre-retirees and retirees, as well as their conception of home were greatly disturbed. The floods also had significant consequences on their behaviour, character and beliefs. A list of recommendations from the victims interviewed to individuals, workers and different government departments shows the need to take into account the emotional distress of victims in implementing emergency measures.

Pollen-mediated gene flow in space is well documented and isolation distances are recommended to ensure genetic purity of Brassica napus seed crops. Isolation in time could also contribute to gene flow management but has been little investigated. We assessed the effects of asynchronous and synchronous flowering on intraspecific B. napus gene flow by seeding adjacent plots of transgenic spring canola cultivars, either resistant to glyphosate or glufosinate, over a 0–4 week interval and measuring outcrossing rates and seed-set. Outcrossing rates, evaluated in the center of the first adjacent row, were reduced to the lowest level in plots flowering first when the seeding interval > 2 weeks. Increasing the time gap increased outcrossing rates in plots flowering second up to a seeding interval of two weeks. Flowers that opened during the last week of the flowering period produced fewer seed (< 10% of total seed production) and a smaller fraction of outcrossed seed (–25%). Observed time gap effects were likely caused by extraneous pollen load during the receptivity of productive seed-setting early flowers. Clearly, manipulation of B. napus flowering development through staggered planting dates can contribute to gene flow management. The approach will need to be validated by additional site-years and increased isolation distances.