Relative contribution of genotype, seed size and environment to secondary seed dormancy potential in Canadian spring oilseed rape (Brassica napus)

Secondary seed dormancy has been linked to seedbank persistence of volunteer oilseed rape (Brassica napus) in western Canada. It has been suggested that there is a genetic component to secondary seed dormancy expression in oilseed rape, but little is known of its importance in relation to non‐genetic factors. In a series of experiments we investigated the relative importance of genotype, seed size, time of windrowing and pre‐ and post‐harvest environment on the expression of secondary seed dormancy. We found that genotype contributed between 44 and 82% to the total variation in secondary seed dormancy. A broad range in secondary seed dormancy expression was observed among 16 genotypes examined. Nevertheless, three‐quarters of the genotypes investigated exhibited relatively high potential for the expression of secondary seed dormancy (back‐transformed mean 71% dormant seeds). Seed size contributed 21% to the total variation, while the influence of seed maturity (harvest regime) on secondary seed dormancy expression was negligible. Despite diverging environmental conditions during the four growing seasons spanning these experiments, the influence of pre‐harvest environment on seed dormancy expression was relatively small and ranged from 0.1% to 4.5%. Secondary seed dormancy potential decreased over time during seed storage. This decrease was greatest when seeds were stored at ambient temperatures and least when seeds were stored at ?70°C.     

Variation in the annual dormancy cycle in buried seeds of the weedy winter annual Viola arvensis

Seeds of Viola arvensis collected in different years and in different months within those years were buried in soil under natural seasonal temperature cycles, and changes in their germination requirements monitored. Seeds were dormant at maturity in May or June, but nondormant by autumn. During winter, some seeds entered dormancy, while others entered conditional dormancy, i.e. retained the ability to germinate at 15/6 and 20/10^oC but not at other thermoperiods. Dormant and conditionally dormant seeds became nondormant the following summer. Seeds collected in 1981 exhibited an annual dormancy:nondormancy cycle, while those collected in 1982 exhibited an annual conditional dormancy:nondormancy cycle. The type of dormancy cycle found in these seed lots during their first year of burial persisted in subsequent years. Thirty–five and 36% of seeds collected in May 1983 and 1986, respectively, were conditionally dormant the following May, while only 5 and 9% of those collected in the same field in June 1983 and 1986, respectively, were conditionally dormant. Dormant seeds collected in 1981,1982 and 1984 and buried at 5^oC during summer germinated to 0, 33 and 0% respectively, at 15/6^oC in autumn. After the 1982 seeds became nondormant during summer, only 25% entered conditional dormancy when buried at 5^oC, but after the 1981 and 1984 seeds became nondormant, 100% entered conditional dormancy at 5^oC. Thus, the persistent seed bank of V. arvensis at a population site may consist of seeds with an annual dormancy:mondormancy cycle and others with an annual conditional dormancy:nondormancy cycle. This is the first report of the two types of annual seed dormancy cycles in the same species.     

Seed germination behavior of glyphosate‐resistant and susceptible Italian ryegrass (Lolium multiflorum Lam.)

Ryegrass (Lolium multiflorum Lam.) is one of the most difficult annual weeds to control in cultivation systems worldwide, especially in temperate regions. The widespread use of herbicides in the past two decades has selected resistant biotypes of ryegrass in crops in Southern Brazil. Ryegrass seeds are dormant when disseminated and germination can be staggered over time (crop‐growing season). Knowledge of the germination behavior of seeds from herbicide‐resistant plants has been little studied, but it would be very useful in integrated weed management. Thus, this study aimed to characterize the dynamics of the soil seed bank of two biotypes of L. multiflorum, one glyphosate‐resistant and the other glyphosate‐susceptible, under a no‐tillage system. The treatments were arranged in a bifactorial scheme, using seeds from biotypes (glyphosate‐resistant and glyphosate‐susceptible) with monthly periods of removal from field (one to 12 months). Seeds of each biotype were placed on the soil surface and covered with soil and straw to simulate no‐till conditions. The percentage of germinated, dormant, and dead seeds was evaluated every 30 days. The ryegrass seed bank of glyphosate‐susceptible and glyphosate‐resistant biotypes was reduced to 11 and 15% of dormant seeds, respectively, at the end of 12 months. However, there was no variation in germination, dormancy, and seed mortality between susceptible and glyphosate‐resistant ryegrass. Seeds of glyphosate‐resistant biotype and susceptible showed germination behavior with similar dynamics in the soil over a period of 12 months.     

Seasonal changes in the germination of buried seeds of Monochoria vaginalis

This study investigates the seasonal variation of germination ability of buried seeds of Monochoria vaginalis (Burm.f.) Presl var. plantaginea Solms. The field-collected seeds were buried in a flooded or an upland field and then exhumed monthly. The exhumed seeds were germinated under four temperature regimes. The seeds exhumed from the flooded soil were dormant at the beginning of burial and proceeded into a conditional dormancy/non-dormancy/conditional dormancy cycle throughout the remaining period of the experiment. The seeds exhumed monthly from the non-flooded soil exhibited an annual dormant cycle, which is dormancy/conditional dormancy/non-dormancy/conditional dormancy/dormancy. At day and night temperatures of 25/20 °C, the exhumed seeds from both the flooded and the upland soil resembled each other in terms of seasonal variation of the germination percentage. In September and October, more seeds exhumed from upland soil failed to germinate under higher temperature than from flooded soil. Strictly avoiding exposure to light during seed exhuming and seed testing prevented the seeds from germinating. A short exposure of the exhumed seeds to light during preparation promoted dark germination when the seeds were at the non-dormant stage. The potential implications of our results for weed management strategies in rice production are discussed.     

Phenotypic selection for seed dormancy in white snakeroot (Eupatorium rugosum)

Eupatorium rugosum (Ageratina altissima), commonly known as white snakeroot, is a weedy plant that invades woodland areas in North America, Korea, and Japan. In order to examine the inheritance of seed dormancy in this species, seeds from a single population were screened for their differential germination response to stratification. After two cycles of recurrent selection, the seed from the shallow–dormant lines had 4.4 times greater germination prior to stratification than did the seed from the deep–dormant lines. The seed from the deep–dormant lines showed 3.4 times greater germination after stratification, compared to the seed from the shallow–dormant selections. This suggests that primary dormancy in the seed of white snakeroot is under some degree of genetic control. This perennial species produces overwintering rhizomes that give rise to adventitious, vegetative buds each spring. The plants selected for the production of seeds with lower levels of dormancy in the fall were observed to generate rhizomatous buds that were released from dormancy earlier in spring, compared to the plants that produced seeds with higher levels of dormancy. A statistically significant positive correlation also was observed between seed and bud dormancy in a naturally occurring population of white snakeroot. Common regulatory elements might be influencing dormancy in both the seeds and vegetative buds of this species.     

Winter annual grassy weeds increase over‐winter mortality in autumn‐sown wheat

Over‐winter mortality, that is, winterkill, reduces cereal crop competitive ability and yield. While management and environmental variables are known to affect winterkill, the extent to which weeds contribute to increased winterkill is largely unknown. Winter annual weeds may increase winterkill through resource competition and by increasing incidence of and damage from plant pathogens that cause winterkill. We evaluated the impact of summer annual (Avena fatua) and winter annual (Bromus tectorum) weeds on the over‐winter survival rate of winter wheat over three winters, during which plots were covered with snow. Pink snow mould (Microdochium nivale), a winterkill pathogen known to infect B. tectorum and winter wheat, was common in wheat stands. In weed‐free treatments, mortality rates were initially near zero, but increased by nearly 45% in each subsequent winter, presumably due to an increase in snow mould disease in continuously cropped winter wheat. Whereas A. fatua infestation had no impact on crop survival rates, winter wheat survival in B. tectorum‐infested plots was 50% less than the weed‐free control in the second and third years of this study. Among B. tectorum‐infested plots, winter wheat over‐winter survival declined with increasing weed seed produced in the previous summer. Overall, this study demonstrated that winter annual weed infestations can reduce crop stand densities below replanting thresholds by reducing fall‐sown cereal winter survival. The effects of winter annual weeds on winter wheat may be meditated by increased proliferation of snow mould disease.     

Seed dormancy and soil seedbank of the invasive weed Chenopodium hybridum in north‐western China

Seed dormancy and persistence in the soil seedbank play a key role in timing of germination and seedling emergence of weeds; thus, knowledge of these traits is required for effective weed management. We investigated seed dormancy and seed persistence on/in soil of Chenopodium hybridum, an annual invasive weed in north‐western China. Fresh seeds are physiologically dormant. Sulphuric acid scarification, mechanical scarification and cold stratification significantly increased germination percentages, whereas dry storage and treatments with plant growth regulators or nitrate had no effect. Dormancy was alleviated by piercing the seed coat but not the pericarp. Pre‐treatment of seeds collected in 2012 and 2013 with sulphuric acid for 30 min increased germination from 0% to 66% and 62% respectively. Effect of cold stratification on seed germination varied with soil moisture content (MC) and duration of treatment; seeds stratified in soil with 12% MC for 2 months germinated to 39%. Burial duration, burial depth and their interaction had significant effects on seed dormancy and seed viability. Dormancy in fresh seeds was released from October to February, and seeds re‐entered dormancy in April. Seed viability decreased with time for seeds on the soil surface and for those buried at a depth of 5 cm, and 39% and 10%, respectively, were viable after 22 months. Thus, C. hybridum can form at least a short‐lived persistent soil seedbank.     

Germination rates of weedy radish populations (Raphanus spp.) altered by crop‐wild hybridisation,not human‐mediated changes to soil moisture

Cultivated plants are known to readily hybridise with their wild relatives, sometimes forming populations with weedier life‐history strategies than their progenitors. Due to altered precipitation patterns from human‐induced global climate change, crop‐wild hybrid populations may have new and unpredictable environmental tolerances relative to parental populations, which would further challenge farming and land‐management weed control strategies. To recognise the role of seed dormancy variation in weed invasion, we compared seedbank dynamics of two cross‐type populations (wild radish, Raphanus raphanistrum, and crop‐wild hybrid radish, R. raphanistrum × R. sativus) across a soil moisture gradient. In a seed‐burial experiment, we assessed relative rates of seed germination, dormancy and seed mortality over two years across cross types (crop‐wild hybrid or wild) and watering treatments (where water was withheld, equal to annual rainfall, or double annual rainfall). Weekly population censuses in 2012 and 2013 assessed the frequency and timing of seedling emergence within a growing season. Generally, germination rates were two times higher and seed dormancy was 58% lower in hybrid versus wild populations. Surprisingly, experimental soil moisture conditions did not determine seedbank dynamics over time. Yet, seed bank dynamics changed between years, potentially related to different amounts of annual rainfall. Thus, variation in seedbank dynamics may be driven by crop‐wild hybridisation rates and, potentially, annual variation in soil moisture conditions.     

How much of seed dormancy in weeds can be related to seed traits?

Seed dormancy contributes to species persistence in unpredictable environments and is a key process to be taken into account in weed dynamics models. As the level of seed dormancy, photosensitivity and the dates of dormancy induction and release are difficult to measure, our objective was to relate weed seed dormancy with morphological, chemical or physiological seed traits and with expert knowledge. Dormancy of four species was studied experimentally during a 2‐year seed burial experiment. Experiments were supplemented with data from the literature to increase the number of species analysed, resulting in a data set of 29 species. Proportions of non–dormant seeds were higher for elongated than spherical seeds, even when accounting for phylogenetic relatedness between species. Elongated seeds, which tend to remain on the soil surface in undisturbed habitats, may have been selected for lack of dormancy and immediate germination to limit mortality due to predation. Dormancy increased with seed coat thickness, which can act as a chemical and physical barrier to germination, while no relation was found with seed lipid or protein content. No correlation was found between photosensitivity parameters and any of the species traits analysed. Variations in dormancy dates (induction and release) were highly correlated with average field emergence season estimated from expert knowledge. The observed correlations suggest that the level of dormancy results both from direct and from indirect effects of traits being involved in trade‐offs together with seed mortality.     

Variation in the development of secondary dormancy in oilseed rape genotypes under conditions of stress

Summary A substantial amount of seed is left in the fields before and during harvest of oilseed rape. Although this crop exhibits little or no primary dormancy, the absence of certain environmental cues that promote germination of imbibed seeds induces secondary dormancy. The work reported investigated the extent to which environmental stress conditions, including osmotic stress, low oxygen stress and anaerobiosis, induce secondary dormancy in oilseed rape, and examined the variation in development of secondary dormancy between and within genotypes. Osmotic stress was most effective in inducing dormancy. Anaerobic treatment produced very few dormant seeds, as did an atmosphere low in oxygen and high in nitrogen. The development of secondary dormancy under osmotic stress varied considerably between and within genotypes. Dormancy ranged from almost zero to about 60% for winter genotypes and about 85% for spring types. Within genotypes, variations occurred between seed lots and years of harvest. Temperature variations affected the percentage of dormant seeds. More dormant seeds were likely to be produced with incubation under water stress at 20 °C than at 12 °C. In winter genotypes, fewer dormant seeds were produced when incubation temperature and germination test temperatures differed. Thus, incubating at 20 °C and 12 °C, followed by germination tests at 20 °C and 12 °C, respectively, produced most dormant seeds. Also, in the winter genotypes, the potential development of secondary dormancy was positively correlated with the pattern and speed of germination of untreated seeds.     

The roles of light and pericarp on seed dormancy and germination in feral Raphanus sativus (Brassicaceae)

The timing of seed germination may determine the success of a weed species in an agroecosystem, and its expression is modulated by environmental conditions, but also by seed physiology and anatomy. The aims of this study were to investigate the roles of light, pericarp, dry storage and cold stratification on seed dormancy and germination in feral radish, a troublesome agricultural weed in temperate zones of the Americas that reduces crop yields. To this end, we used isolated intact pods and extracted seeds to test germination over time under contrasting temperature, light and storage conditions. Here, we showed that fresh seeds were non‐dormant, but that light and the presence of the pericarp reduced germination, especially under low temperatures. The pericarp reduced the final water content absorbed by seeds inside pods and decreased absorption/dehydration rates. The pericarp showed several small lignified cell layers in the endocarp, and x‐ray images displayed the lack of space between the partially embedded seed and the endocarp. Dry storage and cold stratification were ineffective in breaking the dormancy imposed by the pericarp. The apparent requirement for darkness and the mechanical restriction of the pericarp may have the potential to induce dormancy, spreading the timing of seed germination over a more extended period and hindering the control of feral radish.     

A review of the relationship between primary and secondary dormancy,with reference to the volunteer crop weed oilseed rape (Brassica napus)

Fresh seeds of oilseed rape (Brassica napus) are reported to be nondormant and nonphotoblastic. However, a portion of the seeds can be induced into a light‐requiring state (secondary dormancy) for germination and also exhibit dormancy cycling. Thus, if seeds become buried in the soil they can form a persistent seedbank and become a serious volunteer weed in succeeding crops. The capacity of nondormant seeds of B. napus to be induced into secondary dormancy is contrary to results of studies on fresh nondormant seeds of some other species. A reanalysis of published and unpublished data shows that fresh seeds of this species have some degree of primary dormancy and that there is a significant relationship between primary dormancy and the capacity to enter secondary dormancy. However, most germination tests on B. napus have not been done in enough detail to detect primary dormancy (or not) in fresh seeds of this species. The usefulness of information on the relationship between primary dormancy and the capacity of the seeds to enter secondary dormancy is discussed in relation to management of weedy volunteers of this species.     

Influence of hairy vetch seed germination and maturation on weediness in subsequent crops

Hairy vetch is a widely adopted cover crop in the United States. However, hairy vetch can become weedy in subsequent crops as seeds germinate after the cover crop growing season, which is largely attributed to seed dormancy. We conducted two field experiments to determine seed germination, viability and seed production phenology of two common hairy vetch cultivars in Blacksburg and Blackstone, Virginia, US. ‘Groff’ and ‘Purple Bounty’ seed were sown in October 2015 and May 2016 and germination was tracked until June 2017. Subsequently, ungerminated seeds were tested for viability. Both cultivars had <2% germination after the initial germination period, and <1% of seed recovered was still viable at the end of the experiments. We also conducted experiments to determine when these cultivars produce viable seed. Hairy vetch seeds were counted and tested for germination in the spring. Both cultivars produced seed beginning in late‐May, but most seed were not viable until mid‐June in Virginia. Our results indicate that seed dormancy is not the primary cause of hairy vetch weediness in subsequent crops as nearly all germination, 99% of the total germinated seed, occurred during the cover crop growing season. Also, if complete termination occurs before mid‐June in Virginia, it is unlikely viable seed will be added to the seed bank. To better utilise this cover crop species, cultivar selection and proper termination are important to prevent weediness.     

Integrating the herbicide imazapic and the fungal pathogen Pyrenophora semeniperda to control Bromus tectorum

Bromus tectorum is a winter annual grass that affects rangeland in western North America. A glasshouse pot experiment was conducted that integrated imazapic application and inoculation of the soil‐borne fungal pathogen, Pyrenophora semeniperda, for the purpose of providing greater control of B. tectorum. We hypothesised that P. semeniperda inoculation would reduce B. tectorum emergence and integration of imazapic and P. semeniperda would result in a greater reduction in B. tectorum biomass and density compared with either treatment applied alone. This study revealed that P. semeniperda significantly reduced B. tectorum emergence and density and the responses were greatest for seed placed below the soil surface. Further, B. tectorum biomass was similar between imazapic and P. semeniperda treatments. This indicates that P. semeniperda could be applied in advance of B. tectorum germination and emergence. After emergence, imazapic application could reduce B. tectorum biomass and kill seedlings. A two‐pronged approach to controlling B. tectorum that combines P. semeniperda inoculation and post‐emergent imazapic application may provide a greater opportunity to limit invasion of this weed in rangeland of western North America. Future work should be directed towards the pathogen–plant relationship and how it relates to integrating biological control with traditional methods, towards the effect of varying P. semeniperda inoculum and imazapic rates and lastly, to how environmental conditions in the field may affect implementation and efficacy of this two‐pronged approach.     

Does Fusarium‐caused seed mortality contribute to Bromus tectorum stand failure in the Great Basin?

Bromus tectorum (cheatgrass, downy brome) is an important invader in western North America, dominating millions of hectares of former semi‐arid shrubland. Stand failure or ‘die‐off’ is relatively common in monocultures of this annual grass. The study reported here investigated whether soil‐borne pathogens could be causal agents in die‐offs. Soils from two die‐off areas and adjacent B. tectorum stands were used in a glasshouse experiment with sterilised and non‐sterilised treatments. Soil sterilisation did not increase emergence, which averaged 80% in both die‐off and non‐die‐off soils. Seedling biomass was higher in die‐off soils, probably due to increased nitrogen availability. Fusarium was isolated from 80% of killed seeds in non‐sterilised soil treatments. In pathogenicity tests with 16 Fusarium isolates, host seeds incubated under water stress (?1.5MPa for 1 week prior to transfer to free water) suffered over twice the mortality of seeds incubated directly in free water (25–83% with water stress vs. 5–43% without water stress). These results suggest that soil‐borne Fusarium could play a role in B. tectorum stand failure in the field, but that low water stress conditions in the glasshouse experiment were not conducive to high levels of disease. Pathogenic Fusarium isolates were obtained from seeds planted in both die‐off and non‐die‐off soils, suggesting that microenvironmental factors that affect levels of water stress might be as important as relative abundance of soil‐borne pathogens in mediating spatial patterns of disease incidence in the field.     

Real‐time quantitative PCR assays for the rapid detection and quantification of Fusarium oxysporum f. sp. phaseoli in Phaseolus vulgaris (common bean) seeds

Fusarium oxysporum f. sp. phaseoli (Fop) is a devastating pathogen that can cause significant economic losses and can be introduced into fields through infested Phaseolus vulgaris (common bean) seeds. Efficient seed health testing methods can aid in preventing long‐distance dissemination of this pathogen by contaminated seeds. In order to improve detection of Fop in seed, a rapid, accurate and sensitive real‐time PCR assay (qPCR) protocol was developed for detection of Fop in common bean seeds. Seed lots of seven cultivars with infection incidence ranging from 0·25 to 20% were prepared by mixing known amounts of Fop‐infected seeds with Fop‐free seeds. Direct comparisons between SYBR Green and TaqMan qPCR methods were performed using primers based on the Fop virulence factor ftf1. The primers developed in this study produced a 63 bp product for highly virulent strains of Fop but did not produce an amplicon for nonpathogenic or weakly pathogenic isolates of F. oxysporum from P. vulgaris or other hosts. Under optimized conditions, both qPCR assays detected Fop infection at low levels (0·25%); however, the results suggest the TaqMan assay was more reliable at quantification than the SYBR Green assay. Linear regression models were fitted to the relationships between results of qPCR assays and infection incidence, but the models differed among cultivars. Fungal biomass per seed differed among cultivars and was related to seed size. The results indicate that the TaqMan assay developed in this study is a useful tool for the detection and quantification of Fop in bean seeds.     

Quantifying the dormancy of Alopecurus myosuroides seeds produced by plants exposed to different soil moisture and temperature regimes

In pot studies, seeds of Alopecurus myosuroides were less dormant when produced under warm and dry, than under cool and wet conditions. The temperature to which plants were exposed had a greater effect on seed dormancy than soil moisture. The timing of temperature stress had a big impact on initial seed dormancy. The critical period was during seed maturation, irrespective of temperature conditions during the earlier phase of panicle emergence and anthesis. A much higher proportion (57–62%) of seeds collected from fields in 2001, 2003 and 2005 were non‐dormant than in 2002 and 2004 (22–28%). Meteorological records showed that the mid‐June to mid‐July periods in England for 2001, 2003 and 2005 were warmer than average but in 2002 and 2004 were cooler than average. Consequently, results for samples collected from fields support those from experiments conducted under more controlled conditions. Studies in outdoor micro‐plots showed that the differences in seed dormancy recorded with freshly produced seed did affect the rate of germination in the field, 2–3 months after shedding.     

Infection of mungbean seed by Macrophomina phaseolina is more likely to result from localized pod infection than from systemic plant infection

The ubiquitous fungal pathogen Macrophomina phaseolina is best known as causing charcoal rot and premature death when host plants are subject to post‐flowering stress. Overseas reports of M. phaseolina causing a rapid rot during the sprouting of Australian mungbean seed resulted in an investigation of the possible modes of infection of seed. Isolations from serial portions of 10 mungbean plants naturally infected with the pathogen revealed that on most plants there were discrete portions of infected tissue separated by apparently healthy tissue. The results from these studies, together with molecular analysis of isolates collected from infected tissue on two of the plants, suggested that aerial infection of aboveground parts by different isolates is common. Inoculations of roots and aboveground parts of mungbean plants at nine temperature × soil moisture incubation combinations and of detached green pods strongly supported the concept that seed infection results from infection of pods by microsclerotia, rather than from hyphae growing systemically through the plant after root or stem infection. This proposal is reinforced by anecdotal evidence that high levels of seed infection are common when rainfall occurs during pod fill, and by the isolation of M. phaseolina from soil peds collected on pods of mungbean plants in the field. However, other experiments showed that when inoculum was placed within 130 mm of a green developing pod and a herbicide containing paraquat and diquat was sprayed on the inoculated plants, M. phaseolina was capable of some systemic growth from vegetative tissue into the pods and seeds.     

Impact of the pathogen Pyrenophora semeniperda on Bromus tectorum seedbank dynamics in North American cold deserts

Bromus tectorum is a dominant winter annual weed in cold deserts of western North America. We followed patterns of seed carry-over and abundance of the pathogen Pyrenophora semeniperda over 5 years at B. tectorum -dominated shadscale ( Atriplex confertifolia ) and sagebrush ( Artemisia tridentata ) sites in southern Idaho. We hypothesised that more seeds could potentially carry over at the drier shadscale site because of minimal autumn precipitation, but that P. semeniperda , a pathogen that primarily kills dormant seeds, would have more impact at the drier site, where a higher density of dormant seeds would likely be present in the early spring seedbank. Successful first-year seed carry-over was higher in years with below-average autumn precipitation. It was lower at the shadscale site than at the sagebrush site (9% vs.16%). The number of seeds killed during incubation by P. semeniperda averaged three times higher at the drier site and the number of field-killed seeds averaged almost five times higher. This suggests that pathogen-related mortality caused the greater decrease in seed carry-over at the drier site. Mortality risk increased dramatically with seed age. This climate–pathogen interaction apparently limits B. tectorum seedbank carry-over in cold deserts to 3 years or less. Pyrenophora semeniperda shows potential as a biocontrol agent for B. tectorum in these habitats.     

Longevity,dormancy and germination of Cyanus segetum

Cyanus segetum is an iconic, colourful weed in arable fields that provides ecological and societal services. To understand better both the infestation dynamics of C. segetum as an abundant, harmful weed and maintain sustainable populations where it provides beneficial services, we compared information on seed dormancy, seed longevity and germination conditions in two populations. Persistence of seeds buried in the soil was low, with <10% viable after 3 years. Periodic dormancy cycling was observed over the 4 years in the soil, with a maximum of dormant seeds in the spring and a minimum in the autumn; however, 20% of the seeds were non‐dormant all the time. Seeds of C. segetum were positive photosensitive, but light requirement varied among populations. Base water potential for germination was ?1 MPa. Base temperature ranged from 1 to 2°C. Optimum temperature for germination was about 10 to 15°C, but the mean thermal time varied greatly between populations, from 80 to 134 day °C. Photoperiod and temperature combinations had no effect on germination percentage, but both reduced the germination rate. Burial deeper than 2 cm greatly reduced germination and seedling emergence strongly decreased at depths >0.5 cm. No seeds buried deeper than 8 cm emerged. Low seed longevity and a wide range of germination conditions could partly explain the rapid disappearance of C. segetum populations after herbicide application began in western Europe. However, yearly sowing in restoration areas does not seem to be essential.