The Role of Light in the Germination of Naturally Occurring Populations of Buried Weed Seeds

Large populations of viable buried arable weed seeds have beenfound in soil which has been continuously used as pasture forthe last six years. Small numbers of dicotyledonous seedlingswere found to germinate within the grass sward, but did notappear to become established. A disturbance of this soil, ascaused by cultivation, resulted in a large flush of germinationduring the subsequent 4 weeks. Under laboratory conditions only10 per cent of these seedlings emerged in the absence of illumination.Under field conditions there was no germination at all in thedark. A short ‘light-break’ of only 90 sec was sufficientto cause the germination of a large proportion of seeds. Onthe basis of these results it is concluded that the appearanceof all weed seedlings from buried seeds, following cultivation,is dependent upon the exposure of these seeds to light.     

Phytochrome-mediated long-term memory of seeds

The question is how long phytochrome, stored within the cytoplasm of plant diaspores, may stimulate their germination. This question arose from the observation that soil cultivations in darkness for weed control gave inconsistent results. Namely, after a single nighttime or daytime cultivation during spring and summer, differences in weed emergence became hardly detectable after a period of six weeks. However, after nighttime and daytime cultivations in late autumn, emergence differences persisted for up to nine months. To examine whether this differing memory effect is phytochrome-mediated, seeds of Chenopodium album and Stellaria media were sown in pots with wet peat, either in daylight or after sunset. In the latter, seeds were irradiated with far-red light for one day prior to being covered and buried. For more than two years the far-red irradiated seeds produced significantly reduced emergence, indicating that germination and emergence of weeds in the field may be supported by maternal far-red absorbing seed phytochrome B(fr) over several months or even years. This conclusion allows refining of the strategy of lightless tillage.     

Stimulation of weed seed germination by 1–(3-chlorophthalirnido) cyclohexanecarboxamide (AC 94377)

The N-substituted phthalimide, AC 94377, promoted the germination of dry-stored seeds of 17 out of 24 weed species in Petri-dish tests maintained at 22°C. In a further test it was able to substitute for light and/or alternating temperatures in promoting the germination of some species. AC 94377 was more active than GA, in stimulating Solanum nigrum seed to germinate. When mixed with soil in the laboratory, AC 94377 again promoted germination of S. nigrum but the level and persistence of activity differed between soils. In the glasshouse, with soil containing a natural weed seed population, more seedlings emerged from treated than from untreated soil but this number represented fewer than half of the apparently viable seeds present. Field applications of AC 94377 promoted the germination of hand-sown seeds of certain weed species but did not increase the number of seedlings emerging from the natural weed seed bank.     

After-ripening and phytochrome action in seeds of dormant lines of wild oat (Avena fatua)

The effects of a short exposure to red, far-red or alternate red/far-red light on the germination of seeds after-ripened for different periods of time were studied in dormant lines of wild oat ( Avena fatua L.). Three stages were distinguishable in the after-ripening period in the response of germination to light. Seeds stayed dormant and showed no response to light during stage I. Phytochrome-mediated germination was observed in seeds during stage II. The phytochrome action disappeared during stage III, i.e. seeds fully germinated following treatments of all light qualities. When the seeds were imbibed in polyethylene glycol solutions, dark germination was reduced and phytochrome again had an effect, which suggested the involvement of phytochrome in water uptake of the seed.     

An unusual effect of the far-red absorbing form of phytochrome: Photoinhibition of seed germination inBromus sterilis L.

Seeds ofBromus sterilis L. germinated between 80–100% in darkness at 15° C but were inhibited by exposure to white or red light for 8 h per day. Exposure to far-red light resulted in germination similar to, or less than, that of seeds maintained in darkness. Germination is not permanently inhibited by light as seeds attain maximal germination when transferred back to darkness. Germination can be markedly delayed by exposure to a single pulse of red light following 4 h inhibition in darkness. The effect of the red light can be reversed by a single pulse of far-red light indicating that the photoreversible pigment phytochrome is involved in the response. The response ofB. sterilis seeds to light appears to be unique; the far-red-absorbing form of phytochrome (Pfr) actually inhibiting germination.Abbreviations Pr red absorbing form of phytochrome - Pfr far-red absorbing form of phytochrome     

Photomanipulation of phytochrome in lettuce seeds

Seeds of lettuce (Lactuca sativa L. cv. Grand Rapids) were imbibed and given either short irradiation with red or far red light prior to drying or dried under continuous red or far red light. Seeds treated with either short or continuous red germinate in darkness, whereas seeds treated with either short or continuous far red require a short exposure to red light, after a period of imbibition, to stimulate germination. Irradiation of dry red seeds with far red light immediately before sowing results in a marked inhibition of germination. This result was predicted since far red-absorbing form phytochrome can be photoconverted to the intermediate P650 (absorbance maximum 650 nm) in freeze-dried tissue. A similar far red treatment to continuous red seeds is less effective and it is concluded that in these seeds a proportion of total phytochrome is blocked as intermediates between red-absorbing and far red-absorbing form phytochrome, which only form the far red-absorbing form of phytochrome on imbibition. The inhibition of dry short red seeds by far red light can be reversed by an irradiation with short red light given immediately before sowing, confirming that P650 can be photoconverted back to the far red-absorbing form of phytochrome. The results are discussed in relation to seed maturation (dehydration) on the parent plant.     

Phytochrome E Controls Light-Induced Germination of Arabidopsis

Germination of Arabidopsis seeds is light dependent and under phytochrome control. Previously, phytochromes A and B and at least one additional, unspecified phytochrome were shown to be involved in this process. Here, we used a set of photoreceptor mutants to test whether phytochrome D and/or phytochrome E can control germination of Arabidopsis. The results show that only phytochromes B and E, but not phytochrome D, participate directly in red/far-red light (FR)-reversible germination. Unlike phytochromes B and D, phytochrome E did not inhibit phytochrome A-mediated germination. Surprisingly, phytochrome E was required for germination of Arabidopsis seeds in continuous FR. However, inhibition of hypocotyl elongation by FR, induction of cotyledon unfolding, and induction of agravitropic growth were not affected by loss of phytochrome E. Therefore, phytochrome E is not required per se for phytochrome A-mediated very low fluence responses and the high irradiance response. Immunoblotting revealed that the need of phytochrome E for germination in FR was not caused by altered phytochrome A levels. These results uncover a novel role of phytochrome E in plant development and demonstrate the considerable functional diversification of the closely related phytochromes B, D, and E.     

Dark Reversion of Phytochrome in Lettuce Seeds Stored in a Water-saturated Atmosphere

Dark reversion of the far red-absorbing form of phytochrome, which does not occur in dry lettuce (Lactuca sativa var. Grand Rapids) seeds, appears to take place in seeds stored in a water-saturated atmosphere. The water content (approximately 70% after 10 days) of such seeds is insufficient to support germination; however the treatment enhances germination in seeds stored for 1 to 5 days, but this enhancement subsequently disappears, and the effect of extended storage (up to 28 days) is inhibiting. The half-time for dark far red-absorbing phytochrome reversion is 7 to 8 days, and at this time it can be completely reversed by exposing the seeds to a flash of red light. Storage of more than 7 to 8 days decreases red light enhancement of germination.     

The effects of domestic compost upon the germination and emergence of barley and six arable weeds

In a bioassay, leachate from composted household waste was found to decrease both cress germination and the germination of barley and six arable weeds, especially in the light. The effect of compost depth upon the emergence of these species was examined in a glasshouse experiment. Compost had no significant effect on barley emergence. However, weed emergence, particularly of those with small seeds, was reduced greatly by the physical effect of compost and, to a lesser extent, by its chemical effect. The emergence of the large-seeded species was relatively unaffected by increasing depths of compost, whereas that of the smaller-seeded weeds steadily decreased, being almost completely prevented by a 3 cm layer. The use of compost to control arable weeds in the field is discussed.     

Possible significance of changes in the light requirement of Cirsium palustre seeds after dispersal in ash coppice

Abstract. It is demonstrated that after the feelling of ash coppice Cirsium palustre becomes established from seed that was produced during the previous coppice cycle and has lain underground for several years. These seeds are light-requiring and it is probable that their germination is triggered by exposure to light during coppicing in winter.
It is assumed that the seeds become light-requiring because phytochrome in the far-red absorbing form high. This facilitates their incorporation in the seed bank in summer. However, the disappearance of Pfr is inhibited at low temperatures; this means that the seeds can store the light stimulus in winter and will not germinate until they experience higher temperatures in spring. The significance of the inhibition of seed germination under a leaf canopy is that it enhances the seeds chance of being incorporated in the soil seed bank.     

The Induction of Light Sensitivity in Weed Seeds by Burial

Seeds of a number of weed species were buried in soil for aperiod of 50 weeks. At the end of this period the soil was disturbedunder controlled illumination. In three species germinationappeared to be unaffected by light, prior to burial. Followingburial, however, germination took place only in the light, suggestingthe induction of light sensitivity. In eight other species,which showed varying degrees of light sensitivity when freshseeds were examined, germination, following burial, was completelydependent upon exposure to light. Seed germination has also been shown to be inhibited by burialunder laboratory conditions. The extent of this inhibition isdependent upon the depth of burial and the water content ofthe medium. Experiments using artificial aeration indicate thatit is the presence of a gaseous inhibitor in the soil atmospherewhich prevents germination. This inhibitor appears to arisefrom the seeds themselves and is not carbon dioxide.     

Interactions between Mild NaCl Stress and Red Light during Lettuce (Lactuca sativa L. cv Grand Rapids) Seed Germination

The sensitivity of lettuce (Lactuca sativa L. cv Grand Rapids) seeds to red light was reduced by NaCl concentrations which had no effect upon the germination of continuously illuminated seeds. The germination capacity of the seeds was fully restored by increased red light exposures. Indirect evidence indicates that NaCl does not affect the photoconversion of red-absorbing form of phytochrome to the far-red absorbing form of phytochrome. Instead, the increased red light requirements are attributable to increases in the threshold levels of the far-red absorbing form of phytochrome necessary to induce germination and to changes in the slopes of the fluence-response curves. Results also show that the sensitivity of the seeds to NaCl decreased as the time between red light irradiation and the imposition of NaCl stress increased.     

紫茎泽兰土壤种子库特征及其对幼苗的影响

研究紫茎泽兰(Eupatorium adenophorum)土壤种子库特征及其对紫茎泽兰种子的萌发、幼苗命运的影响, 在综合治理紫茎泽兰入侵危害及防止紫茎泽兰的继续扩散等方面有着重要的意义。该文在攀枝花紫茎泽兰入侵严重的地区, 通过采集果园、放牧灌丛以及禁牧灌丛3种不同生境紫茎泽兰土壤种子库的样本, 以说明不同干扰程度下紫茎泽兰种子在土壤中的分布状况。通过野外调查并结合盆栽实验, 初步研究了紫茎泽兰土壤种子库基本特征以及光照和种子在土壤中的埋藏深度等对紫茎泽兰幼苗的影响。结果表明: 1)果园、放牧灌丛和禁牧灌丛等3种干扰程度不同生境的深层种子量占总种子量的比例分别为56.44%、46.96%和24.86% (p=0.006), 这说明土壤深层种子量大小与干扰成正比, 干扰越大, 深层次紫茎泽兰种子量占总种子量的比重越大。2)播种在0、1和5 cm深度的种子萌发率分别为64.67%、22.67%和13.33%, 即种子埋藏越深, 萌发率越低, 不同层次种子萌发率差异极显著(p=0.00); 幼苗死亡率分别为27.95%、0和0, 表层种子萌发的幼苗有较高的死亡率, 而由埋藏在深层的种子萌发的幼苗没有死亡, 土壤表层发芽的幼苗与不同埋藏深度种子萌发的幼苗之间死亡率差异极显著(p=0.00)。3)在无遮蔽、半遮蔽和全遮蔽3种不同情况下, 紫茎泽兰幼苗的死亡率分别为72.15%、30.38%和4.87%, 定居率分别为6.66%、33.99%和46.67%, 即遮蔽程度越高, 死亡率越低, 定居率越高, 不同处理之间死亡率和定居率差异均极显著(p=0.00)。研究结果暗示, 强光可能是导致紫茎泽兰幼苗死亡的重要原因, 人类活动的干扰可能导致更多的紫茎泽兰种子进入土壤深层, 从而改变了紫茎泽兰土壤种子库的结构。由于土壤深层种子比表层种子具有更强的抵抗强光照射等不良环境因子影响的能力, 所萌发的幼苗成活率高, 表明其具有更高的繁殖效率, 因此人类活动干扰是紫茎泽兰入侵后难以根除的原因之一。     

Photocontrol of seed germination in Impatiens wallerana Hook. f.

General characteristics of light sensitivity of Impatients wallerana seeds were investigated. Germination was absolutely dependent on light, irrespective of temperature. High percentages of germination were obtained by exposure to long periods of illumination or, alternatively, to several repeated short irradiations with red light. In this case, responsiveness to light was not altered by increasing either the initial incubation period in darkness or the dark intervals between short exposures. Effects of red light were reversed by far-red light, thus demonstrating the involvement of phytochrome. Evidence was presented for an interactive effect, of unknown physiological nature between red and far-red light on the germination of the seeds.Abbreviations P_r phytochrome, red light absorbing form - Pfr phytochrome far-red absorbing form     

Effect of light environment during soil disturbance on germination and emergence pattern of weeds

This paper describes results from experiments which investigated the effects of light intensity during soil disturbance on germination and emergence pattern of weeds. Different emergence patterns were demonstrated for seeds which are instantly flash induced compared to seeds which are induced to germinate by integrating a weak light signal over a period of time. A reduced and delayed emergence is achieved after a disturbance in darkness compared to a soil disturbance in daylight. The increased emergence after soil disturbance in daylight is due to additional plants originating from seeds placed at a soil depth in the pots where daylight cannot penetrate and induce seeds to germinate, but which are induced during the short exposure period. A close relationship between soil disturbance intensity and number of weed plants emerging was found in field experiments with shallow harrowings. It was also shown that a portion of the increased number of seedlings arising when soil disturbance is carried out in daylight, compared to soil cultivation in darkness, originates from seeds germinating from deeper soil layers, resulting in a deeper average germination depth.     

ENVIRONMENTAL CONTROL OF SEED GERMINATION IN THLASPI ARVENSE (CRUCIFERAE)

The effect of environmental conditions during storage and imbibition on germination was investigated in field pennycress (Thlaspi arvense L.), a weed species that can behave as a winter or a summer annual. Freshly harvested seeds of an inbred line with a cold requirement for flowering exhibited primary dormancy that was rapidly lost following 1 month of afterripening in a dry state. Nondormant seeds were positively photoblastic. The light effect was mediated through phytochrome since germination was promoted by red light and inhibited by far red light. Seedling emergence was also inhibited by light filtered through a canopy of wheat leaves. Germination of field pennycress seeds was considerably more sensitive to moisture stress than two sympatric species, wild oat (Avena fatua L.) and wheat (Triticum aestivum L., cv. ERA). Seeds of the latter two species were chosen in order to compare the effect of water potential on germination in field pennycress with that in sympatric species. It was concluded that the major environmental factor limiting nondormant field pennycress seeds on the soil surface was water availability. Imbibition of fully afterripened seeds at low temperatures (6 C) induced a deep secondary dormancy. In contrast to primary dormancy, cold-induced dormancy was not alleviated by red light, alternating temperatures (21/5 C), or 2 months of dry storage at 6, 15, or 35 C. However, exogenous gibberellin A₃ or 24 weeks of dry storage resulted in germination in cold-induced dormant seeds. Secondary dormancy was not observed in fully afterripened seeds that were preincubated at 21 C for 1 or 2 days prior to the cold treatment. These results may explain the failure in field experiments to observe the cold-induced secondary dormancy that limits spring emergence in other winter annuals (J. Baskin, C. Baskin, Weed Res. 1979 19: 285–292).     

Photocontrol of seed germination in the hemiparasite Buchnera hispida (Scrophulariaceae)

Abstract Buchnera hispida, a facultative root parasite of grasses and graminaceous crops, has a light requirement for germination. Studies were carried out on the effects of varying photoperiods with or without preceding dark incubation, on seed germination. Buchnera seeds showed long-day behaviour, since they germinated at all photoperiods including continuous light, and longer photoperiods were more effective in triggering seed germination than shorter photoperiods. Also, effects of red and far-red light indicated that the phytochrome system is operative in the light-induced germination of Buchnera. Although dark incubation in water before illumination was not absolutely necessary for germination, it caused the seeds to respond more rapidly to light. The longer the time of the dark incubation the more responsive the seeds were to photoperiod except when 15 min light was given. The effectiveness of a preceding dark incubation in making Buchnera seeds sensitive to rapid light action was completely inhibited at 4°C. This is in agreement with the hypothesis that a reaction partner of the far-red absorbing form of phytochrome is produced during dark incubation of Buchnera seeds. Such an intermediate has also been reported in some positively photoblastic seeds of non-parasitic flowering plants.     

Photoinduced Seed Germination of Oenothera biennis L: I. General Characteristics

General characteristics of light-induced germination of Oenothera biennis L. seeds were investigated at 24°C. During dark imbibition, seeds reached maximal respiration in 7 hours and maximal water content and photosensitivity in 24 hours. After dark imbibition of 24 hours, seeds required a long exposure (>36 hours) to red or white light for maximal germination. Two photoperiods (12 and 2 hours) separated by a period of darkness of 10 to 16 hours gave near maximal germination. For the two photoperiod regime, the first light potentiates a reversible phytochrome response by the second light. A 35°C treatment for 2 to 3 hours in the dark immediately prior or subsequent to 8 hours of light caused a higher percentage of germination. A 2 hour treatment at 35°C also potentiates a reversible phytochrome response. Halved seeds germinated at 100% in light or darkness indicating that the light requirement of the seeds is lost in the halving procedure. After-ripened seeds required less light and germinated more rapidly and at higher percentages than seeds tested shortly after maturation.     

Influence of Light on Germination of Pinus palustris Seeds

Red light with a wavelength of 660 nm promotes germination of longleaf pine (Pinus palustris Mill.) seeds, and far-red light (730 nm) inhibits germination. The promotion-inhibition process is repeatedly reversible, indicating that germination is controlled by the photoreversible reaction of phytochrome. Response varied greatly between single-tree lots and was dependent on the length of time seeds were imbibed at 5°C. Dry seeds did not respond to light treatments when they were subsequently imbibed and tested in darkness. Stratification for 28 days essentially removed the light requirements for germination.     

Blue light induced inhibition of seed germination: The necessity of the fruit coats for the blue light response

The seeds (achenes) of Laportea bulbifera require a chilling to break their dormancy and are negatively photoblastic. Their germination is inhibited by both continuous blue light and continuous or prolonged far-red radiation. The germination of de-coated seeds, prepared by removing the fruit coats, however, was strongly inhibited by continuous far-red, but not by continuous blue light. Photoreversible germination by a brief irradiation with red light occurred when the chilled seeds were exposed to prolonged far-red light. These results suggest that far-red light may regulate the germination of L. bulbifera seeds through the phytochrome system which exists in the regions other than fruit coats and that the blue light reaction may be governed by other photoreceptor system(s).