Some effects of competition between Emex australis and E. spinosa

When plants of Emex australis Steinh. and E. spinosa Campd. were grown in pots in monoculture or in competition, there was greater seedling mortality in E. australis. In competition with E. spinosa, E. australis was later-flowering and had lower seed, leaf, root and total dry weights. However, in E. spinosa leaf, stem, seed and total dry weight were greater than they were in mono-culture. The more bulbous root and more erect stems of E. spinosa may be linked with its greater competitive ability. Although at present much more restricted in occurrence in Australia than E. australis, the results suggest that E. spinosa will in time become the dominant species where the two occur together.     

Effect of temperature during burial on dormant and non-dormant seeds of Lamium amplexicaule L. and ecological implications

Spring-produced seeds of Lamium amplexicaule L. were dormant at maturity in May and after-ripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6 and 20/10°C) and non-dormant at high (25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5 and 15/6°C, and non-dormant seeds germinated to high percentages at 5, 15/6, 20/10, 25/15 and 30/15°C. Seeds that became conditionally dormant at 5°C afterripened completely (i.e. became non-dormant) after transfer to 30/15°C. Buried seeds that became non-dormant in a non-temperature-controlled glasshouse during summer were still non-dormant after 12 weeks of storage at 30/15°C, while those stored at 5°C for 12 weeks had entered conditional dormancy. Thus, low temperatures cause reversal of the afterripening that takes place at high temperatures, but not that which takes place both at low and at high temperatures. Low winter temperatures cause dormant autumn-produced seeds and non-dormant seeds in the soil seed pool to become conditionally dormant. The ecological consequences of these responses to temperature are discussed in relation to the timing of seed germination in nature.     

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.     

Temperature requirements for after-ripening in buried seeds of four summer annual weeds

Freshly matured, seeds of the four summer annuals Ambrosia artemisiifolia, Polygonum pensylvanicum, Amaranthus hybridus and Chenopodium album were buried in soil at (12/12 h) daily thermoperiods of 15/6, 20/10, 25/15, 30/15 and 35/20°C and at a constant temperature of 5°C. After 0, 1, 3 and 5 months, seeds of each species at each temperature were exhumed and tested at a 14-h daily photoperiod at all six temperatures. Fresh seeds of A. artemisiifolia and P. pensylvanicum did not germinate at any temperature, those of A, hybridus germinated to 4 and 64% at 30/15 and 35/20°C, respectively, and those of C. album to 11–20% at 25/15, 30/15 and 35/20°C. Seeds of A. artemisiifolia and P. pensylvanicum, which germinate only in spring, required exposure to low (5, 15/6°C) temperature to after-ripen completely (i.e., to gain the ability to germinate over a wide range of temperatures), and little or no after-ripening occurred at high (25/15, 30/15 and 35/20°C) temperatures. Seeds of A. hybridus and C. album, which germinate in spring and summer, required exposure to low temperature to after-ripen completely, but at high temperatures they rapidly gained the ability to germinate at high temperatures. Regardless of the burial temperatures and species, when after-ripening occurred, seeds firs germinated at high and then at low temperatures. The minimum germination temperature for a species decreased with after-ripening temperature and with an increase in the length of the burial period.     

The role of light and alternating temperatures on germination of Polygonum aviculare seeds exhumed on various dates

The annual dormancy cycle was investigated in buried seeds of Polygonum aviculare L. exposed to natural temperature changes in Lexington, Kentucky, U.S.A. Seeds were exhumed monthly from December 1984 to February 1987 and tested in light (14-h daily photoperiod) and continuous darkness at 12/12-h daily alternating temperature regimes of 15/6, 20/10, 25/15, 30/15 and 35/20°C. During autumn and winter, seeds became non-dormant, and in March 1985 they germinated to 95-100% at all thermoperiods in light and to 7-61% in darkness. Seeds remained non-dormant during spring but became more specific in their germination requirements in early summer. During July and August 1985, seeds germinated to 17-53% in light at 30/15 and 35/20°C but to 0-10% at all other test conditions. By September, about 65% of the seeds were dormant, but the others were able to germinate under the higher alternating temperatures in light. A similar seasonal cycle was recorded in the following year through to the spring of 1987. The results confirm the seasonal pattern of dormancy in this species (Courtney, 1968) but indicate that alternating temperatures combined with light are important in determining germination potential in P. aviculare.     

Germination ecology of Emex spinosa and Emex australis,invasive weeds of winter crops

Emex spinosa and Emex australis are invasive dicotyledonous weeds. The effects of various environmental factors on the germination of these weeds were investigated under laboratory and glasshouse conditions. Germination response of both species was lower at warmer temperature, and maximum germination was recorded at 20/12°C (day/night). Light stimulated germination in both species, but considerable germination also occurred under darkness. More than 80% of E. spinosa seeds germinated at pH between 6 and 9, whereas E. australis seeds germination was considerably decreased at pH 9. Emex spinosa was fairly tolerant to salinity as compared with E. australis and germination (21%) of E. spinosa occurred even at 200 mm NaCl. Both species were sensitive to osmotic stress, but E. spinosa tolerated more osmotic stress than E. australis. Temperature above 20/12°C (day/night) and low osmotic potential increased time to start germination and mean germination time (MGT), as well as decreased germination index (GI) of both species. Darkness resulted in increased MGT and decreased GI in both species when compared with 10 h photoperiod. Salt stress strongly increased time to obtain 50% germination and reduced GI of both species. In both species, an increasing burial depth decreased emergence percentage and emergence index and increased time to start emergence, although some seed emerged even at 10 cm burial depth. It was concluded that both species can germinate over a wide range of environmental conditions. However, E. australis was more sensitive under adverse environmental conditions compared with E. spinosa. This information on germination ecology may aid in developing tools and strategies for management.     

Characterization of the germination and emergence response to temperature and soil moisture of Avena fatua and A. sterilis

Seeds of Avena fatua L. and )A. sterilis L. were germinated under a wide range of temperatures (5–30°C) and osmotic potentials (?25 to ?1400 KPa) in order to characterize their responses to these two environmental factors. Although both species behaved similarly at moderate temperatures, different responses were observed at the two extremes. )A. sterilis germinated and emerged in a higher proportion than A. fatua at temperatures below 10°C but the opposite was true at temperatures above 20°C. Although the rates of these two processes were similar in both species up to 18°C, above this temperature the germination and emergence of )A. sterilis was considerably delayed in comparison with that of A. fatua. The effect of decreasing osmotic potentials in reducing the germination was more pronounced in A. sterilis than in A. fatua. However, no differences were observed in the emergence responses of either species. The adaptative advantages of these characteristics and their relationship with the geographic distribution of the two species is discussed.     

Effects of after-harvest period and environmental factors on seed dormancy of Amaranthus species

The effects of seven constant temperatures (10–40°C at 5°C intervals) and seven after‐harvest periods (30–540 days after harvest) were evaluated on seed germination of nine Amaranthus species (A. albus, A. blitoides, A. cruentus, A. deflexus, A. graecizans, A. hybridus, A. lividus, A. retroflexus and A. viridis). Seeds of A. blitoides and A. viridis were also tested at alternating temperatures of 10/30°C (12/12 h thermoperiod) in continuous darkness and in an alternating 12/12 h dark/light photoperiod. With the exception of A. blitoides and A. viridis, germination increased as temperature increased from 20 to 35°C; the latter representing the optimum temperature (70–100% germination). At 10 and 15°C constant temperatures, no significant seed germination occurred in A. albus, A. deflexus, A. graecizans and A. lividus, while in A. cruentus, A. hybridus and A. retroflexus there was no germination at 10°C, but at 15°C more than 60% germination occurred. Germination was influenced strongly by after‐ripening period in A. cruentus, A. hybridus and A. retroflexus, partially in A. deflexus, and barely in A. graecizans and A. lividus. Seeds of A. blitoides and A. viridis required alternating temperatures and light to achieve high germination percentage (>90%). Primary dormancy in Amaranthus plays a fundamental role in extending germination over a longer period, so that the probability of seedling survival is maximised. The present study adds to the understanding of the environmental control and germination ecology of Amaranthus species and provides data that can contribute to predicting weed emergence dynamics.     

A rapid method to identify and quantify soft rot erwinias on seed potato tubers1

Potato tubers are usually contaminated by more than one species or pathovar of soft rot erwinia and, because blackleg incidence is related to the contamination level of seed tubers, the disease potential of seed stocks may be assessed by determining seed-tuber contamination level. A method is described for identifying and quantifying directly from tubers the three soft rot erwinias commonly associated with potatoes. Replicate lots of 10–15 tubers are peeled by dry abrasion in a commercial potato peeler and the peel weight determined by weighing the tubers before and after peeling. Sap is expressed from the peel, an antioxidant (0.075% dithiothreitol) added, and the sap is dilution-plated on a diagnostic selective medium (crystal violet pectate [CVP]). After incubating for 24 h at 20°C, the plates are velvet-replicated onto fresh plates of CVP with or without 35 μg ml^-1 erythromycin and incubated for 48 h at 27°C and 24 h at 33.5 or 37°C. Soft-rot erwinias typically form deep cup-like cavities on CVP and they can be identified and enumerated according to the pattern of cavity formation. Cavities are formed by Erwinia carotovora pv. atroseptica only at 27°C, by E. carotovora pv. carotovora at 27 and 33.5°C but not at 37°C, whereas E. chrysanthemi forms cavities at all temperatures but fails to grow in the presence of erythromycin. Contamination levels can be expressed as the number of different erwinias per tuber or per g peel.     

Germination strategies of annual and short-lived perennial species in the Arabian Desert

Germination timing is highly regulated in short-lived plant species since it strongly influences recruitment success of vegetation. In deserts, the spatiotemporal distribution of plant-available water is highly episodic and unpredictable, making winter months more favorable for seed germination when other abiotic conditions co-occur. We hypothesized that changes in photoperiod and thermoperiod would impact germination more in seeds that had undergone in situ storage. We assessed 21 annual and short-lived perennial species in the Arabian Desert to find (1) if seeds were dormant at maturity, (2) if in situ seed storage increased germination percentage compared with no storage, (3) if photoperiod and thermoperiod germination requirements were influenced by in situ storage, and (4) if a phylogenetic association in seed germination could be observed. Seeds of each species collected in early 2017 were divided into two batches. One was tested for germination within one week (fresh seeds). The other was stored in situ at the maternal location (stored seeds) until October 2017 and tested for seed germination in the first week of November. Seed germination was conducted in incubators at two thermoperiods (15°C/20°C and 20°C/30°C; 12 h/12 h), and two photoperiods (12 and 0 h light per day). Results indicated that seed germination percentages of 13 species were significantly enhanced by in situ storage. A thermoperiod response was exhibited by stored, but not fresh seeds. Light exposure increased germination of fresh seeds but had only a minimal effect on stored seeds. Germination traits exhibited no phylogenetic correlation. This result indicated that selection pressure for germination strategy was stronger than that for taxonomic traits of these desert species.     

Germination ecology of seeds of the annual weeds Capsella bursa-pastoris and Descurainia sophia originating from high northern latitudes

Low temperatures may inhibit dormancy break in seeds of winter annuals, therefore it was hypothesized that seeds of Capsella bursa‐pastoris and Descurainia sophia that mature at high latitudes in late summer–early autumn would not germinate until they had been exposed to high summer temperatures. Consequently, germination would be delayed until the second autumn. Most freshly matured seeds of both species collected in August and September in southern Sweden were dormant. After 3 weeks of burial at simulated August (20/10°C) and September (15/6°C) temperatures, 28 and 27%, respectively, of the C. bursa‐pastoris and 56 and 59%, respectively, of the D. sophia seeds germinated in light at 15/6°C. In contrast, in germination phenology studies conducted in Sweden, only a few seeds of either species germinated during the first autumn following dispersal. However, there was a peak of germination of both species the following spring, demonstrating that dormancy was lost during exposure to the low habitat temperatures between late summer and early autumn and spring. Nearly 100% of the seeds of both species subjected to simulated annual seasonal temperature changes were viable after 30.5 months of burial. In the burial study, exhumed seeds of C. bursa‐pastoris were capable of germinating to 98–100% in light at the simulated spring–autumn temperature regime (15/6°C) in both spring and autumn, while those of D. sophia did so only in autumn. In early spring, however, seeds of D. sophia germinated to 17–50% at 15/6°C. Thus, most seeds of these two annual weeds that mature in late summer do not germinate in the first autumn, but they may do so the following spring or in some subsequent autumn or spring.     

Temperature effects on Eleusine indica and Setana anceps grown in association (I)

Studies were made at Kairi on the Atherton Tableland of Queensland, Australia, on the effects of varying lemperature regimes, both controlled and natural, on the germination of seed of Setaria antcept Stapf. cv. Nandi and Eleusine indica (L.) Gaertn. The germination of E. indica seed was found to be much more temperature labile than that of S. ancepts. The temperature required for peak germination was higher for E. indica seed than for S. ancepts seed. The effects of temperature on competition between E. indica and S. ancepts were studied in the field by varying the time of planting. It was shown that at mean screen temperatures measured throughout the growth period of <23° C, S. ancepts was dominant in mixtures of the two species. At mean temperatures >23° C E. indica was dominant. There was a tendancy for S. aweps yields to decline with increase in E. indica plant density but there was a much closer negative correlation between E indica top dry weight and S. aancepts yield. From the meteorological data for Kairi for the past 25 years predictions were made on the best times to plant S. ancepts to avoid serious competition from E indica.     

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.     

Germination responses of buried seeds of Capsella bursa-pastoris exposed to seasonal temperature changes

Buried seeds of Capsella bursa-pastoris exhibit an annual conditional dormancy/non-dormancy cycle. Seeds after-ripen during summer and remain non-dormant during autumn and winter. Seeds enter conditional dormancy in early spring, first showing marked decreases in ability to germinate at high (35/20°C) and then at lower (30/15, 25/15°C) temperatures. Seeds do not lose the ability to germinate to high percentages at March (15/6°C) and April (20/10°C) temperatures in March and April. Thus, C. bursa-pastoris is a facultative winter annual, germinating in both autumn and spring if seeds are exposed to light. However, because some seeds retain the ability to germinate at 30/15 and 25/15°C, they could do so throughout the growing season in regions with cool, moist summers. Conditional dormancy developed in all seeds given 12 weeks at 5°C and subsequently kept for 4 weeks each at March (15/6°C), April (20/10°C) and May (25/15°C) temperatures. Thus, seeds of C. bursa-pastoris enter conditional dormancy as temperatures increase in spring.     

祁连山保护区种子植物属的区系研究

祁连山自然保护区位于甘肃西南部,祁连山北坡,北纬36°45′—39°30′,东经93°31′—102°40′,面积272.2万hm2,属青藏高原、黄土高原和蒙古高原的过渡带;分布有种子植物1286种,隶属84科431属,占中国种子植物科数的30.43%,属数的13.86%,种数的5.00%。含20种以上的属6属155种,含10-19种的属19属244种,含5-9种的属45属292种,含1-4种的属360属595种,其中,含1种的属217属217种。属的分布类型有12个分布类型和18个分布亚型,热带分布类型有3个类型、1个变型,共27属44种,占祁连山保护区总属数的6.26%;北温带分布及其变型在本区共173属,占本区属数的40.14%,其中北温带分布类型在本区共126属,占29.23%,为本区最大的分布类型;旧世界温带分布及其变型共64属,其中在旧世界温带分布的54属植物中,鹅观草属(Roegneria C.Coch.)为本区最大的属,共15种;地中海区、西亚至中亚分布及其变型共34属,其中地中海区、西亚至中亚分布在祁连山保护区均为含1—5种的小属;中亚分布及其变型共有24属,其中中亚分布中,除(Dilophia Thoms)和小甘菊属(Cancrinia Kar.et Kir.)各有3种外,其余11属均仅含1种;中国特有分布共9属10种,这些特有成分中,有青藏高原特有属(黄缨菊Xanthopappus C.Winkl.)、唐古特地区的特有属(穴丝荠属Coelonema Maxim.),大部分为本区与周围地区所共有的属,而无真正的本区特有属。温带成分占优势,植物区系年轻,草本植物丰富而乔木种类贫乏,特有属、种少,地理成分沿海拔高度明显不同。     

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.     

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 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.     

Effect of temperature on conidial germination, mycelial growth and aggressiveness of the defoliating and nondefoliating pathotypes of Verticillium dahliae from cotton in China

Three defoliating (D) pathotype isolates and five nondefoliating (ND) pathotype isolates of Verticillium dahliae from cotton in central China were tested for adaptation to various temperatures in conidial germination on water agar (10?C33°C), mycelial growth on potato dextrose agar (10?C33°C) and infection of cotton seedlings (Gossypium hirsutum cvs. ??E Mian 24?? and ??Yin Rui 361??) (25?C33°C). Results showed that the D-pathotype isolates adapted better than the ND-pathotype isolates to 30°C for conidial germination and mycelial growth, although the isolates of the two pathotypes had the same optimum temperature of 25°C. Under day/night temperatures of 25/25, 27/27 and 30/25°C for 20 and 25?days, the D-pathotype isolates induced the defoliation syndrome on seedlings of the two upland cotton cultivars, whereas the ND-pathotype isolates did not induce defoliation syndrome. The values for the areas under the disease progress curve (AUDPC) and the vascular discoloration index (VDI) were higher for the D-pathotype isolates than those for the ND-pathotype isolates in each temperature treatment. Under 30/30 or 33/27°C, at least two of the three D-pathotype isolates still had higher AUDPC values and/or VDI values than all the ND-pathotype isolates on E Mian 24. Therefore, the D-pathotype isolates appear more aggressive than the ND-pathotype isolates in infection of cotton. Results also showed that the cotton cultivar Yin Rui 361 was more tolerant than the cotton cultivar E Mian 24 to infection by both pathotypes of V. dahliae. This study suggests that the D-pathotype isolates can well adapt to high temperature and heavily infect cotton under 25?C30°C, and these features might be responsible for the rapid spread of this pathotype in central China.     

Asian spiderflower (Cleome viscosa) germination ecology in southern Iran

Cleome viscosa is one of the most important weeds of warm‐season crops in southern Iran. Laboratory experiments were conducted to assess the impact of environmental factors on seed germination of C. viscosa . Freshly harvested seeds exhibited dormancy that was relieved (>90%) after immersion for 20 min in concentrated sulfuric acid. Regardless of the temperature regime, the final percentage of germination in light/dark (69.3%) was significantly higher than in complete darkness (58.3%). The optimum temperature for germination was 35/25°C in both light and dark. No germination was observed at constant temperatures of either 15 or 45°C. The thermal thresholds for seed germination, the base (T _b) and the mean ceiling germination temperatures (T _c(50)) were estimated to be 18.8 and 39.9°C, respectively. A base water potential ( Ψ _b(50) ) of ?0.96 MPa was identified for C. viscosa seeds. The response threshold of C. viscosa to reduce 50% of maximum germination for salinity was estimated to be 255 mM. Seeds that were placed on the soil surface had the highest percentage of seedling emergence (77.3%), and no seedlings emerged from seeds placed at a depth of 6 cm. The findings of this study could help to improve the integrated weed management strategies for this species.