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.     

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.     

First report of <Emphasis Type="Italic">Ageratum enation virus</Emphasis> infecting <Emphasis Type="Italic">Crassocephalum crepidioides</Emphasis> (Benth.) S. Moore and <Emphasis Type="Italic">Ageratum conyzoides</Emphasis> L. in India

In October 2009, vein yellowing disease was observed on the weeds Crassocephalum crepidioides and Ageratum conyzoides in a subtemperate region in northern India. Ageratum enation virus (AEV), along with a nanovirus like satellite DNA 1, was found to be associated with both weeds. The isolates had 99% identity with each other and with an isolate of AEV reported from Zinnia elegans from this region. To the best of our knowledge, this report is the first of any begomovirus infection in C. crepidioides in India and the first on AEV infecting C. crepidioides worldwide and A. conyzoides in India.     

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.     

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.     

Seasonal changes in the germination responses of buried Lamium amplexicaule seeds

Spring-produced seeds of Lamium amplexicaule L. were buried in pots of soil in an unheated glasshouse in June 1978, and at 1–2-month intervals, for 27 months, they were exhumed and tested for germination in light and darkness at temperatures simulating those in the habitat from early spring to late autumn. Freshly-matured seeds were dormant, but by autumn 85% or more germinated in light at 15/6, 20/10, 25/15 and 30/15°C but only 7% or less in darkness. During late autumn and winter germination in light decreased at 25/15 and 30/15 °C but not at 15/6 and 20/10 °C, and germination in darkness increased at 15/6 and 20/10 °C. During late winter and early spring germination in light at 15/6 and 20/10 °C decreased, and seeds lost the ability to germinate in darkness. By the second autumn of burial, seeds germinated to near 100% in light at 15/6 to 30/15 °C and to 10–25% in darkness at 15/6 and 20/10 °C. The cycle of germination responses was repeated during the second winter and spring and the third summer of burial. Autumn-produced seeds were dormant when buried in November 1979, but by spring they germinated to 81 and 36% at 15/6 and 20/10 °C, respectively, in light. These seeds afterripened further during summer. The consequence of seasonal changes in germination responses is that (1) seeds can germinate in the habitat in late summer, autumn and spring but not in early- to mid-summer or in late autumn and winter and (2) during both germination seasons, seeds produced during the previous spring(s) and/or autumn(s) can germinate.     

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 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.     

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.     

Influence of environmental factors on conidial germination and survival of Sphaeropsis pyriputrescens

Sphaeropsis pyriputrescens is the cause of Sphaeropsis rot in apples and pears. In this study, effects of temperature, wetness duration, relative humidity (RH), dryness, and interrupted wetness duration on conidial germination of the fungus were evaluated. Conidial germination and germ tube elongation occurred at temperatures from 0°C to 30°C. The optimum temperature for germination and germ tube elongation appeared to be 20°C, at which a minimum wetness period of 5 h was required. Conidia germinated at RH as low as 92% after 36 h at 20°C, but not at 88.5% RH. The effect of dry periods on germination depended on RH. Conidial germination at 85% RH was higher than that at 25% RH within a 4-h dry period, after which time no difference was observed. Less than 10% conidia germinated after a 10-day dry period at both 20°C and 28°C. Conidial germination decreased as the wetness duration prior to dryness increased. Conidia wetted for 6 h prior to dryness died within a 1-h dry period. After a 12-h dry period, no or few conidia germinated at 25% RH, whereas 3% to 10% of the conidia germinated at 85% RH and no further decrease was observed as the dry period increased. The results contribute to our understanding of conditions required for conidial germination of S. pyriputrescens and infection of fruit leading to Sphaeropsis rot.     

The influence of temperature on germination of gorse (Ulex europaeus L.)

The germination of U. europaeus seed was investigated at temperatures between 4 and 40°C on a thermal gradient bar. At constant temperature the germination rate increased linearly with temperature from a minimum near 0°C to an optimum at 18°C and then decreased to a maximum at 26°C. At still higher temperatures seeds became imbibed but only germinated when transferred to cooler conditions. Above 35°C viability was lost. The rate of imbibition prior to germination increased with temperature over the whole range. Germination was not increased either by a light treatment or by potassium nitrate. Germination was not stimulated by a wide range of alternating temperature regimes and at mean temperatures below the optimum the germination rate could be adequately predicted from a formula based on performance at constant temperature. At higher temperatures the observed rates became progressively slower than predicted. Seeds from three different sources were tested, all showing similar relationships between germination rate and temperature but differing in the proportion of hard seed. The proportion was least with seed extracted from the soil, intermediate with a collection from the surface and greatest from pods. The findings are discussed in relation to germination in the field following clearing of gorse thicket.     

Arrowleaf sida (Sida rhombifolia) and prickly sida (Sida spinosa): germination and emergence

Maximum arrowleaf sida (Sida rhombifolia L.) germination occurred at 35°C, whereas prickly sida (Sida spinosa L.) germinated to the same extent at 35 or 40°C. Arrowleaf sida germinated better than prickly sida at 20 and 25°C, but did not germinate at 40°C. Less than 50% of seed from both species were viable at 45°C after 21 days of exposure. Both species exhibited more than 75% germination at a range of pH from 5.0 to 8.0. Arrowleaf sida germinated to a greater extent than prickly sida from 0 to —800 kPa, and an osmotic stress of —200 kPa reduced prickly sida germination, whereas —400 kPa was necessary to reduce arrowleaf sida germination. Prickly sida emergence was optimal at a planting depth of 0.5 cm, and declined rapidly at deeper planting depths. However, arrowleaf sida emergence was equivalent at planting depths of 0.5–2.0 cm, with declining emergence below 2.0 cm. Neither species emerged from depths exceeding 5.0 cm. Light did not influence the germination of arrowleaf sida or prickly sida. Sida rhombifolia et Sida spinosa: germination et levee Le maximum du germination pour Sida rhombifolia L. a été atteint à 35°C tandis que Sida spinosa L. a germé de facon équivalente à 35 ou 40°C. S. rhombifolia a mieux germé que S. spinosaà 20 et 25°C, mais n'a pas germéà 40°C. Moins de 20% de graines des deux espèces étaient encore viables à 45°C après 21 jours dèxposition. Les deux especes ont germéà plus de 75% dans des niveaux de pH allant de 5 à 8. S. rhombifolia a mieux germe que S. spinosa de 0 à 800 kPa, et un stress osmotique de —200 kPa a réduit la germination de S. spinosa, tandis que —400 kPa ont été nécessaires pour réquire la germination de S. rhombifolia. La levée de S. spinosaétait optimale à une profondeur de semis de 0,5 cm, et décroissait rapidement à des profondeurs plus élevées. Cependant la levée de S. rhombifoliaétait équivalente pour des profondeurs de 0,5 à 2 cm, avec une baisse à partir de 2 cm. Aucune des deux espèces n'a levéà des profondeurs supérieurs à 5 cm. La lumière n'a pas d'influence sur la germination des 2 espèces. Keimung und Auflaufen der Sidafaserpflanze (Sida rhombifolia L.) und der Stacheligen Samtmalve (Sida spinosa L.) Die stärkste Keimung lag bei der Sidafaserpflanze (Sida rhombifolia L.) bei 35 °C vor, während Samen der Stacheligen Samtmalve (Sida spinosa L.) bei 35 oder 40 °C gleich gut keimten. Samen der Sidafaserpflanze keimten bei 20 und 25 °C besser als die der Stacheligen Samtmalve, keimten jedoch nicht bei 40 °C. Nach Lagerung bei 45 °C für 21 Tage waren die Samen beider Arten zu < 20% keimfähig. Bei pH-Werten zwischen 5 und 8 keimten beide Arten zu >75%. Bei osmotischen Drücken zwischen 0 und —800 kPa keimte die Sidafaserpflanze besser als die Stachelige Samtmalve, deren Keimung ab —200 kPa gehemmt wurde, wahrend bei der Sidafaserpflanze —400 kPa erforderlich waren, die Keimung zu verringern. Samen der Stacheligen Samtmalve keimten am besten in 0,5 cm Tiefe, in gröβerer Ablagetiefe schnell schlechter. Bei der Sidafaserpflanze jedoch waren Aussaattiefen zwischen 0,5 und 2,0 cm gleich gut, erst bei Tiefen unter 2 cm ging der Auflauf zurück. Aus Tiefen unter 5 cm keimte keine der beiden Arten. Durch Licht wurde die Keimung der beiden Sida Arten nicht beeinflußt.     

The effect of temperature on glutathione S-transferase activity and glutathione content in Alopecurus myosuroides (black grass) biotypes susceptible and resistant to herbicides

Herbicide‐resistant populations of Alopecurus myosuroides (black grass) have become widespread throughout the UK since the early 1980s. Previous observations in this laboratory have demonstrated that natural climatic fluctuations caused increases in endogenous glutathione S‐transferase (GST) enzyme activity in A. myosuroides plants as they mature, which is thought to be linked to herbicide resistance in this species. The present study has investigated the effects of plant growth at 10°C and 25°C, and reports GST specific activity and glutathione (GSH) pool size in resistant and susceptible A. myosuroides biotypes. Findings demonstrate differences in GST activity between resistant and susceptible populations, which are transient at lower growth temperatures. The GSH pool size was elevated at lower growth temperature in both biotypes. We speculate that these endogenous responses are part of a natural mechanism of acclimation to environmental change in this species and suggest that resistant plants are more able to adapt to environmental stress, as indicated in this instance by temperature change. These observations imply that the control of resistant A. myosuroides by graminicides may be more effective when applied at lower temperatures and at earlier growth stages.     

Factors affecting seed germination and emergence of Aegilops tauschii

Information on seed germination and emergence ecology of Aegilops tauschii is scant, despite it being a widespread invasive weed in China. We conducted this study to determine the effects of various factors on seed germination and seedling emergence in three A. tauschii populations. Seeds germinated across a wide range of temperatures (5–35°C), with germination of over 90% at 15–20°C. Germination was completely inhibited when dry seeds were exposed to a temperature of 160°C for 5 min; a similar response was observed for pre-soaked seeds at 100°C. Light was neither required for nor inhibited germination. Germination was not significantly affected by pH. Aegilops tauschii was relatively tolerant to low osmotic potential and high salt stress: over 80% of seeds germinated at −0.3 MPa, and all three populations germinated in the presence of 400 mM salt (NaCl) although salt tolerance varied among the populations. Seeds buried at depths of 1–3 cm emerged well, but emergence was completely inhibited at depths greater than 8 cm. The addition of maize straw caused a linear reduction in seedling emergence, although the rate of reduction varied among the populations. The results of this study have contributed to understanding the requirements of A. tauschii germination and emergence and optimising an integrated management system for this weed in Huang–Huai–Hai Plain of China. In addition, our study provides data for development of models to predict the geographical distribution of this weed.     

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.     

Seed banks of some arable soils in the English midlands

Numbers of viable seeds in the 0–15 cm soil layer were determined for 64 arable fields, mainly heavy soils cropped with cereals and leys, in north Oxfordshire and south Warwickshire. When first sampled in 1972 or 1973, there was a range from 1500 to 67 000 seeds m^?2 with a median of 4360 m^?2. Seeds of Poa annua L. occurred in all fields, often in large numbers (up to 35 550 m^?2), while Polygonum aviculare L., Stellaria media (L.) Vill., Bilderdykia convolvulus (L.) Dumort., Aethusa cynapium L., Alopecurus myosuroides Huds., Veronica persica Poir., Chenopodium album L., Veronica arvensis L. and Capsella bursa-pastoris (L.) Med. also occurred frequently. When the fields were sampled again 2 and 4 years later many showed little change either in total seed bank or in species representation. The most pronounced fluctuations involved the annual grasses A. myosuroides, which tended to increase where winter cereals were grown, and P. annua which increased where leys were established. The results are discussed in relation to crop management and compared with those from other surveys. Les stocks de graines dans quelques sols arables des Midlands d'Angleterre Le nombre des graines viables présentes entré 0 et 15 cm de profondeur a été déterminé pour 64 sols arables, principalement des sols lourds occupés par des céréales et des prairies temporaires, dans le nord de l'Oxfordshire et le sud du Warwickshire. Lors de la première estimation, en 1972 ou 1973, les comptages ont donné de 1500 à 67 000 graines m^?2 avec une médiane de 4360. Des graines de Poa annua L. ont été trouvées dans tous les champs, souvent en grand nombre (jusqu'à 35 550 m^?2); on a aussi trouvé fréquemment des graines de Polygonum aviculare L., Stellaria media (L.) Vill., Bilderdykia convolvulus (L.) Dumort., Aethusa cynapium L., Alopecurus myosuroides Huds., Veronica persica Poir., Chenopodium album L., Veronica arvensis L. et Capsella bursa-pastoris (L.) Med. Beaucoup de dénombrements opérés 2 et 4 ans plus tard n'ont montré que peu de changements du nombre total de graines ou de la représentation des diverses espèces. Les fluctuations les plus notables ont été observées à propos des graminées annuelles A. myosuroides, qui tendaient à s'accroitre dans les cultures de céréales, et P. annua, qui augmentait dans les prairies temporaires. Les résultats sont discutés en relation avec la conduite des cultures et comparés avec ceux d'autres dénombrements. Samenvorrat in einigen Ackerböden in Mittelengland In den obersten 15 cm von 64, meist schweren, mit Getreide oder Grasgemischen bepflanzten Ackerböden im nördlichen Oxfordshire und südlichen Warwickshire wurde die Anzahl keimfähiger Samen bestimmt. Bei der ersten, 1972 oder 1973 erfolgten, Bestandesaufnahme wurden zwischen 1500 und 67 000, im Mittel 4360 Samen m^?2 gezählt. In allen Böden wurden Samen von Poa annua L., oft in sehr grosser Zahl (bis zu 35 550 m^?2), gefunden. Häufig waren auch Polygonum aviculare L., Stellaria media (L.) Vill., Bilderdykia convolvulus (L.) Dumort., Aethusa cynapium L., Alopecurus myosuroides Huds., Veronica persica Poir., Chenopodium album L., Veronica arvensis L. und Capsella bursa-pastoris (L.) Med. 2 und 4 Jahre später durchgeführte Zählungen zeigten in vielen Fällen nur geringe Veränderungen, sowohl in Bezug auf Samenzahl als auch auf vorhandene Arten. Die markantesten Aenderungen wurden bei anuellen Gräsern festgestellt; so zeigte A. myosuroides eine zunehmende Tendenz auf mit Wintergetreide bepflanzten Flächen, während P. annua in höherer Anzahl auf Flächen gefunden wurde, wo Grasland angelegt worden war. Die Ergebnisse werden in Bezug auf Kulturmethoden und Fruchtwechsel diskutiert und mit den Resultaten anderer Untersuchungen verglichen.     

A pollen test to detect ACCase target‐site resistance within Alopecurus myosuroides populations

This study was conducted to determine a suitable medium for in vitro germination of Alopecurus myosuroides pollen and to develop a reliable test for the rapid screening of ACCase target site‐resistant plants within populations. The assay is based upon germination of pollen in a medium supplemented with ACCase inhibitors. A 0.25% agar medium, containing 200 mg L^–1 CaNO₃, 100 mg L^–1 H₃BO₃, 200 g L^–1 sucrose, was selected as a suitable medium for in vitro pollen germination. At 25 °C, this medium supported a mean germination rate of 85% within two hours. Plants highly resistant (Rh) to aryloxyphenoxypropionate (APP), owing to the expression of an insensitive ACCase, were found to express this resistance in their pollen. In contrast, plants moderately resistant (Rm) to APP herbicides, owing to an enhanced capacity to detoxify herbicides, did not exhibit this resistance in their pollen. Concentrations of 120 μM fenoxaprop and 1000 μM clodinafop were selected as the best for reliable discrimination of the target‐site‐resistant biotypes. At these concentrations there was more than 50% germination of the Rh pollen grains whereas less than 10% of the S and Rm pollen grains germinated. This test, using haploid material, may also permit distinction between homozygous‐ and heterozygous‐resistant individuals.     

Seed dormancy and periodicity of seedling emergence in Veronica hederifolia L.

Emergence of Veronica hederifolia seedlings began in mid-October and continued into spring; few appeared from June to September. Ripe seeds shed in June were dormant but wben buried in soil outdoors developed a capacity for germination initially at low temperatures (constant4 C; daily alternations of 4-10° and 4-1 5 C) and later at somewhat higher temperatures, with peak germination in September-November. During winter, spring and early summer thc germination capacity declined, to increase again in late summer and early autumn. Cyclic physiological changes thus occur in seeds of V,hederifolia present in the soil, with which lhe consistent seasonal periodicity of seedling emergence is associated. In dry storage ihe capacity for germination progressively increased, but alter 12 months there was a sharp decline in germination at 4° C. Few seeds germinated at 20° C, but moistening with GA 4/7; brought about complete germination at this temperature.     

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.     

Role of temperature in regulating timing of germination in soil seed reserves of Lamium purpureum L.

Fresh seeds of Lamium purpureum L. were dormant at maturity, and when buried and exposed to natural seasonal temperature changes they exhibited an annual dormancy/non-dormancy cycle. During burial in summer, fresh seeds and those that had been buried for 1 year afterripened and thus were non-dormant by September and October; light was required for germination. During autumn and winter seeds re-entered dormancy, and during the following summer they became non-dormant again. Dormant seeds afterripened when buried and stored over a range of temperatures, becoming conditionally dormant at low (5, 15/6°C) and non-dormant at high (20/10, 25/15, 30/15 and 35/20°C) temperatures. Conditionally dormant seeds germinated to high percentages at 5, 15/6 and 20/10°C, while non-dormant seeds germinated to high percentages additionally at 25/15, 30/15 and 35/20°C. Low temperatures caused non-dormant seeds to re-enter dormancy, while high temperatures caused a sharp decline in germination only at 30/15 and 5°C. The temperature responses of L. purpureum seeds are compared to those of L. amplexicaule L.