Comparison of light-regulated seed germination in Ficus spp. and Cecropia obtusifolia: ecological implications

The major components of annual seed deposition in the rain forest at Los Tuxtlas, Veracruz, México are seeds of the pioneer tree species Cecropia obtusifolia and those of some species of Ficus. Cecropia obtusifolia Bertol. forms a relatively persistent viable soil seed bank, whereas seeds of Ficus are seldom found in the soil. Both genera require light for seed germination; however, the species differ in their germination responses to far red (FR) light under laboratory and field conditions. Seeds of C. obtusifolia did not germinate in low red/far red (R/FR) or pure FR, whereas seeds of the Ficus species did. This suggests that Ficus seeds do not become dormant under the light conditions (low R/FR ratio) beneath the leaf canopy of the rain forest. This difference may explain why the species differ in their presence in the soil seed bank.     

Target seed moisture content,chilling and priming pretreatments influence germination temperature response in Alnus glutinosa and Betula pubescens

Abstract

The response of common alder [Alnus glutinosa (L.) Gaertn.] and downy birch (Betula pubescens Ehrh.) seeds to germination temperature was examined following chilling and priming. Seeds of two seed lots of each species were subjected to combinations of chilling (4±1°C) and priming (20°C) treatments in fully imbibed (FI) state or a lower target seed moisture content (TMC) level (30% and 35% in alder and birch, respectively). After treatment, the seeds were allowed to germinate for 56 days at constant temperatures of 7.5, 10, 15, 20, 25 or 30°C. The response to temperature and pretreatment differed between species, but the effect was consistent in each seed lot within each species. In alder, the TMC seeds germinated well across the full range of temperatures, whereas there was an optimum temperature (22–23°C) for seeds given the FI pretreatment. Priming had no significant effect on the germination response of the TMC seeds in alder, but priming greatly improved germination in the FI seeds, especially at the lower germination temperatures (optimum 18–19°C). In contrast, in birch, the TMC seeds germinated better across the full temperature range, but the optimal germination temperature (15°C) was the same for all seed pretreatments. Priming improved germination in both the FI and TMC seeds in birch.     

Seed germination and seedling establishment of Neotropical dry forest species in response to temperature and light conditions

A study was conducted to examine the germination requirements of Cedrela odorata, Guaiacum sanctum and Calycophyllum candidissimum seeds, and the effect of light intensity on survival and growth of C. Odorata and G. Sanctum seedlings planted on open, partially-open and beneath the canopy of a dry forest in Nicaragua. The results show that germination of C. Candidissimum seeds was significantly higher in light than darkness at constant temperatures ranging from 20–35oC. Both C. Odorata and G. Sanctum seeds germinated in light and darkness to a varying extent, and the optimal germination temperature was around 20-25oC. Alternating temperature regimes did not improve germination. Survival of G. Sanctum seedlings was 70% beneath the canopy and 80% in the open, and its relative growth rate in collar diameter was 1.88 mm/month in the open and 1.42 mm/month in the understory. Survival was generally poor for C. Odorata, particularly in the understory. We concluded that light is an absolute requirement for the germination of C. Candidissimum seeds while germination of C. Odorata and G. Sanctum seeds are more sensitive to temperature. Owing to its high survival rate on open site, G. Sanctum could serve as a candidate species for reforestation of degraded sites.     

Improving the collection and germination of West African <Emphasis Type="Italic">Garcinia kola</Emphasis> Heckel seeds

Garcinia kola is highly used as chew-stick for dental care in West Africa, but it is nearly commercially extinct in nature. To help find methods to increase rate and percentage of germination, we investigated its seed germination responses by using several collections and pre-treatments. Seeds processed from 6-week old green fruits did not germinate, whilst those of 10-week old partly-mature, at the intermediate stage through full development, germinated 46%. Seeds from orange mature fruits reached maximum 54–62% germination. Radicles emerged 6 weeks after sowing and normal germination with emergence of the primary single shoot growth occurred after 12 weeks. There was no significant difference (P ≥ 0.05) between germination responses of seeds from Ghana and Cote d’Ivoire. Seeds did not germinate when dried to below ca. 30% MC. De-coating seeds or soaking intact seeds in a 70% ethanol solution increased germination to 82–92%, and also increased germination rate; however germination was not uniform. Because difficulties in germinating these seeds stem from the physical presence of the seed coats and the slow growth of the embryos contained therein, we recommend that fresh seeds from mature fruits be de-coated and immediately sown in preferably, an aerated medium (e.g., sawdust) for cultivation.     

Effects of livestock on seed germination of guava (Psidium guajava L.)

This paper reports on the effects that livestock have on seed germination of guava (Psidium guajava L.). Experiments here reported were intended to simulate gastric scarification using different soaking periods in a 0.01 N HCl solution alone or combined with rumen treatments. Additional experiments evaluated germination of defecated and nondefecated seeds germinated in petri dishes and in cow dung.Passage through the digestive tract of cattle did not affect seed germination of guava. Lowered germination was obtained for seeds germinated in cow dung as compared to laboratory germinated seeds. Nevertheless this difference may reflect an inadequate surface-volume ratio of the cow pat used. Large variations in germination between years were recorded. Nothing is known about the effects this may have on the ecology of pasture invasion by guavas.     

Effect of harvest date,drying, short-term storage and freezing after chilling on the germination of rowan seeds

The effects of seed pretreatment and harvest date on the germination of European rowan (Sorbus aucuparia L) seeds were examined. In one experiment, seeds were subjected to drying, storage, soaking, warm and chilling treatments after harvesting in mid- and late August. In another experiment, fully imbibed (FI) seeds were given warm treatment for six weeks and then various durations of chilling (4?±?1°C) for up to 24 weeks. Thereafter, the seeds were adjusted to target moisture content of 35% and 30% or remained in the FI state and were then subjected to either subsequent chilling or freezing (?3°C) for up to 32 weeks. The treated seeds were allowed to germinate at a constant 15°C with 8 hours of lighting per day. Treatment effects were generally consistent for each harvest date. Seeds did not germinate unless they were chilled and germination rates were low unless the seeds were soaked. Warm treatment applied before chilling appeared to induce dormancy. The effect of storage varied with harvest date and storage treatment, with germination being highest for seeds harvested in late August. Mild freezing of ≥16 weeks duration following 16–24 weeks initial chilling resulted in >80% germination, more than could be achieved using chilling alone.     

Regulation of Picea abies seed dormancy by red and far‐red light at various moisture contents

The effects of red (R), far‐red (FR) and R + FR light on Norway spruce seed dormancy were studied at five different moisture contents (MC) between 5 and 20%. The degree of dormancy was studied by germinating seeds over a wide range of temperatures in the dark. The non‐irradiated control seeds were shallowly dormant, only a proportion of them germinated and within a limited temperature range. Red light progressively stimulated germination between 5 and 17% MC, but this effect was reversed if a FR treatment followed, although all germination could not be inhibited by one FR pulse. Far‐red light had a slightly stimulating effect at 19% MC. To generate seeds able to germinate over a wide range of temperatures in darkness, an artificial light pretreatment should be given to seeds at MC above 17% in order to receive maximum response.     

Seed germination and seedling development in the mango (Mangifera indica L.)

Mango (Mangifera indica L., cv Ruby) seeds taken from ripe fruit showed no dormancy. They germinated at temperatures between 5 and 40 degrees C, but germination was most rapid near the upper end of this range (25-40 degrees C). The fresh seeds had a high moisture content (85%, dry weight basis) and quickly died on dehydration. The optimal temperature for growth of the seedlings was close to 30 degrees C. High temperatures (40 degrees C) and temperatures below 15 degrees C were lethal. Growth of the stem occurred in successive flushes separated by rest periods. When the leaves of the preceding flush finished growing, the axis lengthened beneath the apical bud.     

Predispersal seed predation in Acacia macrostachya,its impact on seed viability,and germination responses to scarification and dry heat treatments

Predispersal seed predation among individual Acacia macrostachya trees over two sites in Burkina Faso was assessed. In addition, the effects of seed predation on seed viability; germination responses to scarification (mechanical, hot water at 60, 70 and 80°C, and sulphuric acid for 10, 20 and 30 min) and dry heat (at 60, 70 and 80°C for 15, 30 and 60 min each) treatments were investigated under laboratory conditions. The results indicated a large difference in predation intensity among individual trees, as well as between sites. Predispersal predation significantly decreased seed germination, particularly when the number of insect larvae per seed increased. Scarified and unscarified seeds germinated equally well, except for hot water treatments of high temperature. This indicates lack of physical dormancy and dispersed seeds can readily germinate provided that conditions for germination are conducive. Seeds exposed to dry heat treatments also germinated close to 97% under low intensity and short exposure times. This suggests that fire, under natural condition, plays a key role in triggering germination of A. macrostachya seeds.     

Germination traits and adaptive regeneration strategies of the threeCarpinus species

Germination tests in the three sympatricCarpinus species,C. laxiflora, C. tshonoskii, andC. cordata, were carried out to clarify their germination traits in relation to the regeneration strategies. Seeds did not germinate just after ripening under any conditions in the three species. After one or two rounds of cold stratification, however,C. laxiflora andC. tshonoskii showed high germination percentages (>80%) at alternating temperature in light whileC. cordata did not. After a long-term (10 months) cold stratification, about 100% ofC. cordata seeds germinated, although about 70% of these seeds were in “conditional dormancy” and cannot germinate in the dark. Seed germination in the threeCarpinus species was enhanced by alternating temperature, but not by light exposure. These results suggest that the seeds of the three species are dormant just after ripening and the dormancy is broken by cold stratification. with intra-generic variations in the breakage. Germination traits in each species may be closely related to the regeneration strategy;C. cordata maintains a persistent seed bank with seed dormancy and regenerates after disturbances as a seed bank strategist, whereas the other two species germinate in the next spring after seedfall and regenerate depending either on existing disturbed-sites or sites of recent disturbances after seedling establishment as a seed rain strategist (C. tschonoskii) or seedling bank strategist (C. laxiflora). This study was supported by grants from the Ministry of Agriculture, Forestry and Fisheries (BCP-97-III-A).     

The effect of different pre-sowing seed treatments, temperature and light on the germination of five Senna species from Ethiopia

The germination requirements of five Senna species: S. bicapsularis, S. didymobotrya, S. multiglandulosa, S. occidentalis and S. septemtrionalis have been investigated. Seeds possess dormancy which is caused by their hard seed coats hampering maximum, uniform and rapid germination. To overcome this dormancy, seeds of the five species were pre-treated with (a) mechanical scarification, (b) concentrated sulphuric acid for 15, 30, 45 and 60 minutes and (c) boiling water for 15, 30, 45 and 60 seconds. To determine the effects of temperature on the germination of seeds, pre-treated seeds from each species were incubated at 10, 15, 20, 25 and 30°C. Germination was also tested in the dark. Both acid treatment and mechanical scarification resulted in fast and uniform germination. The highest germination (95–100%) for all species was obtained from seeds treated with sulphuric acid for 60 minutes. Mechanical scarification resulted in 100% germination in all the species except S. septemtrionalis (59%). Boiling water improved germination significantly in S. didymobotrya (98%), S. occidentalis (82%) and S. septemtrionalis (97%), but had very little effect on S. multiglandulosa and reduced germination in S. bicapsularis. Senna seeds germinated over a wide range of temperatures with the optimum temperatures for germination falling around 20–25°C. Germination was either completely inhibited or very low at 10°C. Seeds of all species germinated both in light and dark conditions.     

Freezing tolerance of conifer seeds and germinants

Survival after freezing was measured for seeds and germinants of four seedlots each of interior spruce (Picea glauca x engelmannii complex), lodgepole pine (Pinus contorta Dougl. ex Loud.), Douglas-fir (Pseudotsuga menziesii (Mirb.) Franco) and western red cedar (Thuja plicata Donn ex D. Donn). Effects of eight seed treatments on post-freezing survival of seeds and germinants were tested: dry, imbibed and stratified seed, and seed placed in a growth chamber for 2, 5, 10, 15, 20 or 30 days in a 16-h photoperiod and a 22/17 degrees C thermoperiod. Survival was related to the water content of seeds and germinants, germination rate and seedlot origin. After freezing for 3 h at -196 degrees C, dry seed of most seedlots of interior spruce, Douglas-fir and western red cedar had 84-96% germination, whereas lodgepole pine seedlots had 53-82% germination. Freezing tolerance declined significantly after imbibition in lodgepole pine, Douglas-fir and interior spruce seed (western red cedar was not tested), and mean LT50 of imbibed seed of these species was -30, -24.5 and -20 degrees C, respectively. Freezing tolerance continued to decline to a minimum LT50 of -4 to -7 degrees C after 10 days in a growth chamber for interior spruce, Douglas-fir and lodgepole pine, or after 15 days for western red cedar. Minimum freezing tolerance was reached at the stage of rapid hypocotyl elongation. In all species, a slight increase in freezing tolerance of germinants was observed once cotyledons emerged from the seed coat. The decrease in freezing tolerance during the transition from dry to germinating seed correlated with increases in seed water content. Changes in freezing tolerance between 10 and 30 days in the growth chamber were not correlated with seedling water content. Within a species, seedlots differed significantly in freezing tolerance after 2 or 5 days in the growth chamber. Because all seedlots of interior spruce and lodgepole pine germinated quickly, there was no correlation between seedlot hardiness and rate of germination. Germination rate and freezing tolerance of Douglas-fir and western red cedar seedlots was negatively correlated. There was a significant correlation between LT50 after 10 days in the growth chamber and minimum spring temperature at the location of seedlot origin for interior spruce and three seedlots of western red cedar, but no relationship was apparent for lodgepole pine and Douglas-fir.     

Effects of storage conditions on dormancy and vigor of Picea abies seeds

The dormancy and vigor of Picea abies seeds were studied after five months of storage at 25 and 75% relative humidity (RH) and 5 and 12 °C. Dormancy was evaluated by studying germination response to light and moist chilling at 12 and 21 °C. Dormancy causing germination reduction in the dark was induced in seeds during storage at 25% RH (5–6% moisture content, MC) in darkness. The dormancy was greater when seeds were germinated at 12 than at 21 °C and after storage at 12 than at 5 °C. The effective dormancy relief by light indicates that germination was under phytochrome control. Moist chilling could partly replace light. According to accelerated aging and leachate conductivity tests, dry seeds could be stored at 12 °C for five months without affecting their vigor. After storage at 75% RH (11% MC) and 5 °C, the seeds germinated slowly and incompletely. The decreased germination response to light indicates that other processes than those mediated directly by phytochrome restricted germination of these seeds. The positive germination response to moist chilling suggested that secondary dormancy was induced in the seeds. However, vigor tests gave some evidence of simultaneous decrease of vigor. Storage at 75% RH and 12 °C decreased germination nearly to 0%. Germination of seeds stored at 75% RH could be stimulated by a short accelerated aging period.     

Seed dormancy and germination of Ficus lundellii and tropical forest restoration

We investigated seed dormancy and germination in Ficus lundellii Standl. (Moraceae), a native species of Mexico's Los Tuxtlas tropical rain forest. In an 8-h photoperiod at an alternating diurnal (16/8 h) temperature of 20/30 degrees C, germination was essentially complete (96%) within 28 days, whereas in darkness, all seeds remained dormant. Neither potassium nitrate (0.05-0.2%) applied continuously nor gibberellic acid applied either continuously (10-200 ppm) or as a 24 hour pretreatment (2000 ppm) induced germination in the dark. Germination in the light was not reduced by a 24-h hydrochloric acid (0.1-1%) pretreatment, but it was reduced both by a 24-h pretreatment with either H(2)O(2) (0.1-5 M) or 5% HCl, or by more than 5 days of storage at 40 degrees C (4.5% seed water content). In a study with a 2-dimensional temperature gradient plate, seeds germinated fully and rapidly in the light at a constant temperature of 30 degrees C, and fully but less rapidly in the light at alternating temperatures with low amplitudes (< 12 degrees C) about the optimal constant temperature. The base, optimal and ceiling temperatures for rate of germination were estimated as 13.8, 30.1 and 41.1 degrees C, respectively. In all temperature regimes, light was essential for the germination of F. lundellii seeds.     

Differentiation of seed germination traits in relation to the natural habitats of three <Emphasis Type="Italic">Ulmus</Emphasis> species in Japan

Germination traits of three Japanese Ulmus species, including two summer-fruiting species, U. davidiana var. japonica (UD) and U. laciniata (UL), and an autumn-fruiting species, U. parvifolia (UP), were investigated. Germination tests that controlled light (16 h dark–8 h light/24 h dark) and temperature (alternating 20–30°C/constant 23°C) conditions were conducted just after seed dissemination. Under the preferred (light and alternating temperature) conditions, UD germinated quickly and percentage germination was high (99%), whereas UL and UP germinated moderately to slowly (65.2 and 23.8%, respectively) and the remaining seeds were primarily dormant. When the seeds were exposed to unsuitable conditions for germination, secondary dormancy was induced in all three Ulmus species. Because primary and secondary dormancy of these species was not strict, the existing dormancy could be released by moist conditions and low temperature during the winter. Thus, all three Japanese Ulmus can germinate either just after seed dissemination or in the following spring. Nevertheless, the predominant germination of summer-fruiting UD just after seed dissemination seems to be advantageous for finding safe sites that might become available after a large-scale fluvial disturbance. Similarly, the delayed germination of autumn-fruiting UP until the following spring seems to be advantageous for preventing germination at the end of the growing season. Summer-fruiting UL had a more negative response to favorable light conditions just after seed dissemination, which seems to be advantageous for establishment in canopy gaps. These germination traits seem to be adaptive responses to the dominant disturbance regimes of their natural habitats.     

Seed Size as a Predictor of Germination Success and Early Seedling Growth in ‘Hollong’ (Dipterocarpus macrocarpus Vesque)

In species with seeds losing viability shortly after dispersal and exhibiting inherently low germination, quick decisions are required with respect to seeds that should be selected to maximize germination success and vigorous growth of seedlings. In ‘hollong’ (Dipterocarpus macrocarpus Vesque), I address the following questions: (a) are seeds that germinate randomly distributed within a seed population, (b) are subpopulations of viable and non-viable seeds separable, (c) does seed size predict which seeds germinate and (d) does seed size predict time required for germination and seedling vigour? Two estimators of seed size, diameter and weight, demonstrated a significant positive linear relationship endorsing assumption that accumulation of mass increases with increase in diameter of seeds. A threshold for selection of potential seeds for germination could not be derived from diameter measurements since seeds in an entire range of diameter did or did not germinate. All seeds <11 g did not germinate, but this threshold lies at the far lower end of the weight range and allows rejection of only a few seeds and acceptance of many seeds that will not germinate. A risk of potential seeds being rejected or non-viable seeds being picked exists if selection was derived from either diameter or weight. However, viable seeds could be better predicted from a scatter-plot of diameter on x-axis and weight on y-axis. Seeds showed a fan-shaped scatter and those developing the lower blade of the fan did not germinate while those following the handle were successful. Hence, two subpopulations segregated, but with a fuzzy edge. Mean diameter and mean weight of germinated seeds were significantly greater than those of ungerminated seeds. Most ungerminated seeds were those that had relatively smaller weight compared to their diameter. Although some large diameter seeds with small weight did germinate, but failed to develop into seedlings. Germination time and seedling vigour parameters (height, leaf number and collar diameter) were correlated both with diameter and weight. However, weight appears to have mattered more than diameter in germination success and early seedling growth.     

杜鹃花种子休眠打破技术的研究

以杜鹃花的两个种映山红（R.simsiiPlanch.）和蓝荆子（R.mucronulatumTurcz.）的种子为实验材料,用不同浓度的硫酸、有机溶剂和氧化剂处理种皮并分别处理不同时间,在培养皿中进行萌发对比实验;用赤霉素、层积及变温处理种子在培养皿中进行萌发的对比实验。结果表明,40%硫酸处理种皮20min、100%乙醚处理种皮20min、5%次氯酸钠处理种皮30min、层积处理及10%赤霉素处理24h均能有效提高映山红种子萌发的发芽率、发芽势和发芽指数;20%硫酸处理种皮10min、层积处理和赤霉素处理能显著提高蓝荆子种子发芽率、发芽势和发芽指数,100%乙醚处理10min能明显著提高蓝荆子种子的发芽率。     

Germination response of alder and birch seeds to applied gibberellic acid and priming treatments in combination with chilling

The effects of seed moisture content (MC), gibberellic acid (GA₃) concentration, chilling and priming pretreatments on the germination of common alder (Alnus glutinosa) and downey birch (Betula pubescens) seeds were examined. After treatment, the seeds were allowed to germinate for 42 days at 15 °C or 20 °C (dark)/30 °C (light). Treatment responses were similar at both temperatures and in both species. GA₃ treatment of seeds in fully imbibed (FI) state for 30 days, or at the lower, target moisture content (TMC) for 30–90 days, significantly improved germination, but longer treatment periods reduced it (FI seeds) or had no effect (TMC seeds). Priming for two days improved germination in the FI seeds, but more than 4 days reduced it. Priming for up to 14 days had little effect on the germination of the TMC seeds.     

Viability of litter-stored Pinus taeda L. seeds after simulated prescribed winter burns

Stratified loblolly pine (Pinus taeda L.) seeds were placed at three depths in a reconstructed forest floor and subjected to simulated prescribed winter burns. Within the forest floor, pine seeds were placed at the L/upper-F interface, upper-F/lower-F interface, and lower-F/mineral-soil interface. Wind was generated by electric box-fans. Seeds that survived the burns were transferred to moist sand flats for 30-day germination tests. About 96% of seeds placed at the two upper layers in the forest floor were either destroyed by the fires or failed to germinate. Germinative capacity of seeds placed at the lower-F/mineral-soil interface averaged 79% as compared to 97% for unburned control seeds.     

Effects of KNO3 pretreatment and temperature on seed germination of Sorbus pohuashanensis

We characterized the effects of KNO3 pretreatment and germination temperature on dormancy breaking and germination of mature mountain ash seeds. Seeds treated with KNO3 and germinated at 25 ℃ followed by 5 ℃ had significantly higher germination percentages and germination potentials (51% and 49%, respectively), compared with controls. These treated seeds also exhibited reduced germination initiation times (minimum of 48 days), and elevated germination rate indices (up to 97). The germination of seeds subjected to long-term cold storage (2 years at 0-5 ℃) was also significantly improved by 3 days of 4% KNO3 pretreatment before germinating under a variable temperature regimen (5 ℃ followed by 25 ℃, and followed by 5 ℃). Germination percentages and germination potentials for these cold-stored seeds reached 67% and 54%, respectively, and the germination rate index increased to 126.99. Pretreatment of mountain ash seeds with KNO3 represents a practical, effective, and pollution-free method for improving germination, and can be implemented easily within a variety of nursery settings.