Factors affecting seed germination and emergence of button grass (Dactyloctenium radulans) (R.Br.) P.Beauv.

Button grass (Dactyloctenium radulans) is a native, widely spread summer grass weed species in Australia. However, limited information is available on the seed germination biology of this species. Experiments were conducted to evaluate the effect of environmental factors on the germination and emergence of two populations of D. radulans. The seeds of these populations were collected separately from Dalby, Queensland and Coleambally, NSW. Seeds were germinated at a range of constant and alternating temperatures (25/15, 30/20, 35/25 and 40/30°C day/night). The greatest seed germination was at a constant temperature of 30°C. Seed germination was reduced at the lowest alternating temperature (25/15°C). Germination of both populations was strongly stimulated by light, suggesting a great amount of emergence of D. radulans on bare ground, such as crop seedbeds. Germination of the D. radulans population collected from a northern cotton farming system (Dalby) was more tolerant to a greater range of salt stress than the population sourced from the south (Coleambally). Seeds of both populations germinated over a wide range of pH, between 4 and 10. However, germination was the greatest in a high pH buffer solution, indicating that the species prefers to germinate in alkaline soil. These results showed that D. radulans seeds possess a wide range of tolerance mechanisms to different environmental stresses. Information obtained in this study will help in developing more sustainable and effective integrated weed management strategies for the control of this weed and weeds with similar responses in summer cropping systems, such as cotton.     

Dormancy,germination and emergence of Urochloa panicoides regulated by temperature

Urochloa panicoides is an annual weed of summer crops. In Argentina, in subhumid areas with monsoon rainfall, it germinates and establishes in a single flush. To (i) identify the environmental factors that modify its seed dormancy level and germination and (ii) quantify the parameters describing the thermal behaviour of the germination and emergence dynamics of this weed under non‐limiting water conditions, we established a set of germination experiments performed (i) under controlled conditions using seeds after ripened for 3 or 6 months in different thermal and hydric conditions and (ii) under field conditions, where the soil temperature was modified by applying different shading levels. Seed dormancy level remained high with 3 months after ripening in all treatments. After 6 months, seeds stored at 4°C in dry conditions did not germinate at any temperature, while seeds stored at 25°C in dry conditions and in situ germinated c. 20% and 60% respectively. Germination percentage was higher in seeds harvested before their natural dispersal. The base, optimum and maximum temperatures for seed germination were 6, 35 and 45°C respectively. Shading reduced the number of emerged seedlings, possibly by reducing the soil thermal amplitude. The results explained the dormancy‐breaking mechanism of U. panicoides that allows a high germination rate in the field when rainfall occurs.     

Germination characteristics of Amaranthus quitensis as affected by seed production date and duration of burial

Thermal requirements for the germination of Amaranthus quitensis, a common annual weed in Argentina, were studied. In addition, temporal changes in dormancy from seeds produced at different times during the growing season were examined. For this second objective, thermal and light requirements for germination were tested in seeds buried at different depths, with or without crop residues. Base and optimum temperatures for germination rates were 12.8°C and 37°C respectively. At dispersal time, maximum percentage germination was 60–70% and this was generally recorded at 35°C/25°C in a 14-h photoperiod. Seed germination tended to increase in later seed collection dates. Seeds of A. quitensis showed seasonal changes in germinability in the soil. In winter, germination of retrieved seeds increased to over 90% until summer, after which there was a decrease until the following winter when germination was close to 40%. There were no differences in germinability between burial depths and crop residue levels. Germination requirements for alternating temperatures and light tended to disappear after burial. Initial viability was 99% and declined slightly during burial. Soil temperature seems to play a crucial role not only by regulating seasonal changes in dormancy, but also by defining the percentage and the germination rate in non-dormant seeds.     

Inter‐ and intrapopulation variation in dormancy of Oryza sativa (weedy red rice) and allelic variation in dormancy‐linked loci

Oryza sativa (weedy red rice), the same species as cultivated rice, is a serious problem in rice production worldwide. Seed dormancy contributes to its persistence. We determined the effect of germination temperature and after‐ripening period on germination capacity (GC) of red rice seeds from Arkansas rice fields in three production zones. We also determined the gene diversity (GD) of dormancy‐linked loci among selected populations. The germination behaviour was evaluated at three temperatures (1°C, 15°C and 35°C) and four after‐ripening periods (0, 30, 60 and 90 days) in two independent experiments. Germination response to temperature and after‐ripening time differed among and within populations in each production zone. Overall, populations from the Delta and Grand Prairie were more dormant than those from White River. Regardless of ecotype or production zone, incubation at 35°C (mean GC = 84–100%) favoured the germination of seeds after‐ripened for 60 days. Germination of these seeds was most variable at suboptimal temperature (15°C), with mean GC ranging from 44 to 97%; at 1°C, none of the seeds germinated. Primary dormancy was released in the majority of populations after 90 days of after‐ripening. Blackhull populations generally had lower mean GC than strawhull populations, regardless of temperature, and required longer after‐ripening time to release dormancy. They also showed a higher inter‐ and intrapopulation variation in germination and after‐ripening than strawhulls and had the highest gene diversity (GD = 0.55–0.58) among test populations. Non‐dormant strawhulls were most distant (D = 0.63) from dormant blackhulls. Ecotype influenced genotypic clustering more than the dormancy trait.     

Germination ecology of Leptochloa chinensis: a new weed in the Italian rice agro-environment

Leptochloa chinensis is a new weed that has been found with increasing frequency in Italian rice paddies. The germination ecology of L. chinensis seeds was studied in order to investigate the development mechanisms and survival strategy of this weed in rice paddies of northern Italy. Leptochloa chinensis seeds showed no dormancy and exhibited germination even in anoxic conditions. Germination was strongly influenced by temperature (minimum around 15°C; optimal 25–35°C) and light (phytochrome dependent). Temperature fluctuation caused an increase of seed germination in the dark. Seed burial also strongly inhibited germination and emergence of this species. At 5 cm seed burial only 5% of seedlings emerged in flooded conditions, while at the same depth, but with no flooding, no seedling emergence was observed. This phenomenon was not due to oxygen depletion, as germination was not inhibited by complete anoxia, as demonstrated by the fact that some seedlings did emerge in flooding conditions when water was no deeper than 6 cm. Seed burial and concomitant flooding induced an unusual germination: first coleoptile emergence and subsequently emergence of the radicle was observed. The possible exploitation of this knowledge for weed management is discussed.     

Modelling Chloris virgata germination and emergence under different temperature and light quality conditions

Chloris virgata is a problematic weed around the world. Prediction of weed germination rates could be a useful strategy to optimise timing of weed control actions. We studied the germination and emergence of C. virgata collected seeds under different after-ripening treatments and different exhumation dates after seed dispersal, to estimate seed dormancy level and predict weed emergence dynamics under field conditions. Three experiments were conducted under controlled conditions to determine base, optimum and maximum germination temperatures (T_b, T_o and T_m respectively) and comprised: (a) exposure of seeds to gradually increasing and decreasing temperatures between 5 and 35°C; (b) exposure of seeds to different constant temperatures; and (c) exposure of seeds to different light quality conditions (red – far red ratio) and temperature regimes (constant and alternating temperatures). To explore genuine environmental conditions, a field experiment was performed to determine weed emergence under different shading levels. Finally, with the data obtained, a thermal time model for dormancy release was used to predict C. virgata seedling emergence in the Argentine Pampas region. Seeds after-ripened in cold and wet conditions and constant 25°C showed the highest germination percentages. The values of T_b (7°C), T_o (28°C) and T_m (40°C) remained constant at all exhumation dates. Neither light quality nor thermal regime modified the final germination percentages. However, shading delayed seedling emergence under field conditions, even when it was adjusted by thermal time. These results may allow predicting C. virgata emergence in temperate regions and help to improve weed control in integrated weed management strategies.     

Seed germination, seedling establishment and growth patterns of wrinklegrass (Ischaemum rugosum Salisb.)

Several laboratory and glasshouse experiments were conducted to assess seed germination, seedling establishment and growth patterns of wrinklegrass (Ischaemum rugosum Salisb.) influenced by temperature and light regimes, and chemical media. Wrinklegrass was a positively photoblastic species, and seed germination was temperature‐dependent and light‐mediated. Seeds soaked in distilled water for 24 h, or oven‐dried at the respective temperature regimes of 15, 20, 25, 30, 35, or 40°C prior to treatment in distilled water and incubated in darkness, failed to germinate. Likewise, no germination prevailed when the seeds were exposed to similar temperature regimes and treated with 0.2 m KNO₃, 5% H₂O₂ or 0.01 m HNO₃, and incubated under continuous darkness. Seeds treated with 5% H₂O₂ at 30°C, or oven‐dried and treated with 0.01% M HNO₃ at 35°C registered 10 and 20% germination. Approximately 75 and 90% of the light‐exposed seeds for all treatments germinated in the first three and six days at 25°C. No germination occurred at 15°C in the first three days after treatment. Seeds subjected to 40°C for six days after treatment recorded 36% germination. The optimum temperatures for seed germination were 25–30°C. Seed drying and soaking treatments widened the windows of the optimal temperatures for wrinklegrass germination. The acidic media of KNO₃, H₂O₂ or HNO₃ favored seed germination. Less than 5% of seed germination occurred with burial or water inundation at depths exceeding 2 cm. Seed burial or inundation at ≥2 cm depths inhibited seed germination. Seeds sown onto moist paddy soils registered ca. 50% germination. Free‐floating seeds on the water surface registered ca. 98% germination within the first six days after seeding. The mean number of seedlings that survived was inversely proportional to water depths, with close to 100% mortality at the 14 cm depths of inundation. Both plant height and seedling survival were linearly proportional to the amount of root mass of seedlings which penetrated the soil. The weed was a prolific seed producer (ca. 6000 seeds/genet or 18 000 seeds/genet per year). The vegetative and reproductive efforts of each wrinklegrass plant registered values of 0.68 and 0.32, respectively.     

Seed dormancy,germination, emergence and seed longevity in Galinsoga parviflora and G. quadriradiata

Galinsoga quadriradiata (hairy galinsoga) and Galinsoga parviflora (smallflower galinsoga, gallant soldier) are very troublesome weeds in many vegetable row crops in Europe. To optimise management strategies for Galinsoga spp. control, an in‐depth study of germination biology was performed. Germination experiments were conducted to evaluate the impact of light and alternating temperatures on germination of a large set of Galinsoga populations. Seedling emergence was investigated by burying seeds at different depths in a sandy and sandy loam soil. Dormancy of fresh seeds harvested in autumn was evaluated by studying germination response in light at 25/20°C with and without nitrate addition. Seed longevity was investigated in an accelerated ageing experiment by exposing seeds to 45°C and 100% relative humidity. Galinsoga spp. seeds required light for germination; light dependency varied among populations. Seedling emergence decreased drastically with increasing burial depth. Maximum depth of emergence varied between 4 and 10 mm depending on soil type and population. In a sandy soil, emergence percentages were higher and seedlings were able to emerge from greater depths than in a sandy loam soil. Freshly produced G. parviflora seeds, harvested in autumn, showed a varying but high degree of primary dormancy and were less persistent than G. quadriradiata seeds that lack primary dormancy. Lack of primary dormancy of freshly harvested G. quadriradiata seeds and light dependency for germination may be used to optimise and develop Galinsoga management strategies.     

Factors affecting the seed germination and seedling emergence of redflower ragleaf (Crassocephalum crepidioides)

Redflower ragleaf (Crassocephalum crepidioides) is a weed, as well as a minor vegetable, in tropical and subtropical regions of the world. The influence of environmental factors and seed conditions on the germination and emergence of redflower ragleaf have been evaluated in order to help understand its distribution and to develop effective management strategies. The seeds germinated at a constant temperature in the range of 10–30°C and reached a maximum at 15–20°C. The highest germination rate was recorded at an alternating temperature of 20/15°C (day/night). The seeds germinated over a wide pH range (2–12), with the highest germination rate at between 4 and 10. Germination under saturated and flooded conditions was also high. The germination of seeds from opened (mature) capitula was significantly higher than from partially opened or unopened capitula. The germination of seeds without a pappus was significantly higher than for seeds with a pappus. The germination rate of 1 year old seeds decreased drastically when compared to that of freshly harvested seeds. The seedling emergence rate was ～63% for those seeds placed on the soil surface, but no seedling emerged from a depth of ≥1 cm. These results indicate that redflower ragleaf seeds can germinate in various environmental conditions, but that the percentage that germinates will be different in different environments. Regeneration could be effectively prevented by at least a 1 cm soil covering or by destroying the plant before the capitula open. In contrast, freshly harvested seeds from opened capitula should be sown on the soil surface when redflower ragleaf is to be cultivated as a vegetable.     

Dormancy studies in three populations of Poa annua L. seeds

Seeds of Poa annua from original collections in Louisiana, Maryland and Wisconsin were grown together in Louisiana over a 3-year period. The freshly harvested seeds and samples stored in moist soil at 30°C were tested for germination at a range of temperatures to compare dormancy and germination characteristics. Seeds of the Louisiana population were dormant over the germination temperature range of 5–25°C, and imbibed storage for 2 weeks did not break dormancy. Freshly harvested seeds of the Maryland population germinated well (78%) at 10°C. With 1 week of imbibed storage at 30°C, germination was good over the range from 5 to 15°C and near 50% at 20°C. Storage for 2 weeks had little further effect. Freshly harvested seeds of two Wisconsin populations germinated above 50% throughout the range of temperatures, and imbibed storage for 2 weeks at 30°C had no effect on germination. The variations in the dormancy of freshly harvested seeds and the varying responses of dormancy breaking from storing imbibed seeds at 30°C suggests that these populations have adapted to avoid high summer temperatures in Louisiana and Maryland but to grow as a summer annual in Wisconsin.     

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.     

Karrikins promote germination of physiologically dormant seeds of Chrysanthemoides monilifera ssp. monilifera (boneseed)

Physiological dormancy in weed species has significant implications for weed management, as viable seeds may persist in soil seedbanks for many years. The major stimulatory compound in smoke, karrikinolide (KAR₁), promotes germination in a range of physiologically dormant weed species allowing targeted eradication methods to be employed. Control of Chrysanthemoides monilifera ssp. monilifera (boneseed), a Weed of National Significance in Australia, may benefit from adopting such an approach. In this study, we hypothesised that seeds of C. monilifera ssp. monilifera exhibit physiological dormancy, germinate more rapidly as dormancy is alleviated, show fluctuations in sensitivity to KAR₁ and form a persistent soil seedbank. Seeds responded to 1 μM KAR₁ (40–60% germination) even during months (i.e. March, April, July, August) when seeds were observed to be more deeply dormant (control germination: 7–20%). Seeds germinated readily over a range of cooler temperatures (i.e. 10, 15, 20, 20/10 and 25/15°C) and were responsive to KAR₂ (~50% germination) as well. Eradication efforts for C. monilifera ssp. monilifera may benefit from use of karrikins to achieve synchronised germination from soil seedbanks, even at times of the year when C. monilifera ssp. monilifera seeds would be less likely to germinate, allowing more rapid depletion of the soil seedbank and targeted control of young plants.     

Factors affecting seed germination and emergence of Gomphrena perennis

Controlled growth chamber experiments were conducted to determine factors affecting seed germination and emergence of the troublesome weed Gomphrena perennis. The objective of this research was to examine the effects of temperature, light, moist chilling, osmotic potential, dry storage and depth of seed burial on G. perennis germination and emergence. The optimum temperature for germination was around 15–20°C. Seeds showed germination rates above 90% under 20/10 and 25/15°C temperature regimes. The minimum exposure to light needed to stimulate germination was 1 min. However, the light requirement was reduced after a long storage period. Furthermore, germination was high (>90%) in all moist‐chilling treatments tested. Germination was highly sensitive to increasing osmotic stress. The highest germination percentage (94%) was achieved at 0 MPa, and decreasing osmotic potential from 0 to ?0.3 MPa reduced germination to 11%. The highest seedling emergence occurred for seeds placed from 0 to 1 cm deep, and no seedlings emerged from a 5‐cm burial depth. Gomphrena perennis has a suitable environment in a no‐till soybean field, where seeds remaining on the surface have the required temperature, light and depth needed for germination.     

Influence of environmental factors on seed germination and emergence of Iresine diffusa

Iresine diffusa has become more abundant under no‐till soyabean in Argentina. The influence of temperature, light, cold‐wet storage, osmotic potential, dry storage and depth of seed burial on germination and emergence of I. diffusa was examined in a growth chamber experiment. Iresine diffusa seeds germinated at the highest proportion (>0.80) in all fluctuating day/night temperatures tested. Conversely, under a constant temperature regime, maximum germination rates occurred at 15 (0.78) and 20°C (0.82), and minimum germination rates occurred at 10 (0.19) and 30°C (0.36). Seed germination was not influenced by light exposure. However, germination decreased after 12 (0.76) and 16 (0.65) weeks in cold‐wet storage. To reduce germination significantly, ?0.4 MPa of osmotic potential (induced by PEG‐6000) or 120 mmol L^?1 of salt (NaCl) concentration was required. Seeds of I. diffusa showed high viability (0.85) after 720 days of dry storage. Low emergence was recorded for seeds buried at 2 cm, and seedling emergence was completely inhibited when seeds were buried at 5 and 10 cm. Iresine diffusa seeds had high viability and were capable of emerging in a broad range of environmental conditions. The thermal germination conditions, shallow soil depths and high moisture conditions in germination phase for I. diffusa are congruent with the conditions in Argentina no‐tillage soyabean. Thus, no‐tillage could provide better conditions for germination than conventional tillage systems. However, due to the fact that I. diffusa can reproduce by rhizomes, further research should be conducted to understand the relative importance of the vegetative reproductive strategy in relation to the presence and persistence of this weed in fields.     

Seed germination ecology of creeping mannagrass (Glyceria acutiflora) and response to POST herbicides

Creeping mannagrass is a perennial grass weed widely distributed in China and is becoming increasingly problematic in nurseries and landscapes in some regions. Understanding the germination ecology and response to commonly available POST herbicides of this weed is critical to determining its adaptive capabilities and potential for infestation, and assist in the development of effective control strategies. In the light/dark regime, creeping mannagrass germinated over a wide range of temperatures (15/5 to 30/20°C), with maximum germination at 20/10°C (95%). No seed germinated at 35/25 or 10/0°C. The time required for 50% of maximum germination increased as temperature decreased. Compared with the light/dark conditions, germination was slightly stimulated when seeds were placed in the dark. Creeping mannagrass is moderately tolerant to osmotic and salt stress, which had 53 and 50% germination rates at ?0.6 mPa osmotic potential and 200 mM NaCl concentration, respectively. Seedling emergence of the seeds buried at a depth of 0.5 cm (86%) was higher than those sowing on the soil surface (17%), but declined with burial depth increasing. There were no differences in the emergence rates from a burial depth 0.5–2 cm. Few seeds (4%) could emerge when seeds were sowed at a depth of 8 cm. POST application of haloxyfop‐R‐methyl, quizalofop‐p‐ethyl, sethoxydim, and pinoxaden provides 100% control of creeping mannagrass at the three‐leaf to five‐leaf stages. To achieve 80% control with clodinafop‐propargyl, mesosulfuron‐methyl, and fenoxaprop‐p‐ethyl, herbicides had to be applied at the three‐leaf stage.     

Factors affecting weed seed germination and seedling growth in lowland rice in Indonesia

Experiments were carried out in Indonesia to see whether weeds of lowland rice fields could be managed by manipulation of the water table and what factors affected germination of their seeds. It was found that seeds of two Scirpus spp. germinated when buried in anaerobic soil but not when on the surface, whereas seeds of two Echinochloa spp. germinated when on the surface of both aerobic and anaerobic soils but when buried germinated only in aerobic soil. The germination of weed seeds was affected to differing extents by submergence in water at depths down to 20 cm. Germination of Fimbristylis littoralis seeds was greatly reduced and of Ludwigia hyssopifolia was complétély inhibited by submergence. Conversely, germination of Monochoria vaginalis seeds was virtually unaffected. It is suggested that the effect of submergence on germination of some species may be due to their reaction to the amplitude of temperature fluctuation. The germination and emergence of seedlings under water were greatly reduced by a cover of Salvinia molesta. The practical importance of these findings is discussed.     

A high temperature requirement for after ripening of imbibed dormant Poa annua L. seeds

Freshly harvested seeds of Poa annua L. collected in south Louisiana were stored in moist soil at seven temperatures between 5°C and 35°C. At monthly intervals, seed lots were removed and germinated at each of the seven temperatures. Seed were dormant for at least 1 month at all test temperatures. Seeds stored for 2 months at 30 and 35°C showed conditional dormancy; there was 100% germination at 10 or 15°C, and poorer germination at 5 or 20°C. Seeds started to lose viability after 2 months at 35°C and were dead after 7 months. In seeds stored at 10–30°C, there were increased percentages and a wider range of germination temperatures as storage time or storage temperatures increased. Seeds stored at 10°C remained dormant for 9 months, but by 12 months of storage the seeds germinated only at 5 or 10°C. Nearly all seeds stored at the same temperatures in air dry soil remained dormant for 6 months, regardless of storage temperature. These results differ from other reports of low temperatures breaking seed dormancy in Poa annua L. and suggest an adaptation to subtropical climates.     

Germination,emergence, and persistence of Sonchus oleraceus,a major crop weed in subtropical Australia

Sonchus oleraceus (common sowthistle) is a dominant weed and has increased in prevalence in conservation cropping systems of the subtropical grain region of Australia. Four experiments were undertaken to define the environmental factors that favor its germination, emergence, and seed persistence. Seeds were germinated at constant temperatures between 5 and 35°C and water potentials between 0 and ?1.4 MPa. The maximum germination rate of 86–100% occurred at 0 and ?0.2 MPa, irrespective of the temperature when exposed to light (12 h photoperiod light/dark), but the germination rate was reduced by 72% without light. At water potentials of ?0.6 to ?0.8 MPa, the germination rate was reduced substantially by higher temperatures; no seed germinated at a water potential >?1.0 MPa. Emergence and seed persistence were measured over 30 months following seed burial at 0 (surface), 1, 2, 5, and 10 cm depths in large pots that were buried in a south‐eastern Queensland field. Seedlings emerged readily from the surface and 1 cm depth, with no emergence from below the 2 cm depth. The seedlings emerged during any season following rain but, predominantly, within 6 months of planting. Seed persistence was short‐term on the soil surface, with 2% of seeds remaining after 6 months, but it increased with the burial depth, with 12% remaining after 30 months at 10 cm. Thus, a minimal seed burial depth with reduced tillage and increased surface soil water with stubble retention has favored the proliferation of this weed in any season in a subtropical environment. However, diligent management without seed replenishment will greatly reduce this weed problem within a short period.     

Temperature requirements for germination of buried seeds of Aethusa cynapium L.

Freshly-collected mature mericarps of Aethusu cynapium were dormant, but some germinated at alternating (16 h low/8 high) temperatures when the seed coverings were removed. Burial during winter increased percentage germination and the temperature range over which it took place. In late spring the range narrowed, first at low and then at higher temperatures, widening again in autumn. Moist storage at both low (4°C) and high (30°C) temperatures overcame dormancy, but exposure to 30°C inhibited subsequent germination at low temperatures. Germination of intact mericarps was consistently lower than that of de-coated seeds. The cyclic change in dormancy status of the seeds appears to interact with the restricting effects of the seed coverings and perhaps other factors in determining the consistent pattern of spring emergence in A. cynapium.     

Germination of proximal and distal seeds of Poa trivialis L. from contrasting habitats

Seeds of Poa trivialis L. were collected from one grassland and two arable habitats. Seeds from the grassland population were less dormant than the arable populations. Distal (upper) seeds were consistently more dormant than proximal (basal) seeds. Dry storage at 4°C and 15°C for 4 weeks after shedding resulted in a slightly greater loss of dormancy than storage at 23°C. Germination was enhanced by subjecting seeds stored at 15°C to repeated hydration and dehydration cycles. Germination of P. trivialis seeds was density-dependent. Germination of distal seeds was particularly impaired at high densities. The ecological implications of these results are discussed in relation to seed survival strategies.