EFFECT OF STRATIFICATION TEMPERATURE AND GERMINATION TEMPERATURE ON GERMINATION AND THE INDUCTION OF SECONDARY DORMANCY IN COMMON RAGWEED SEEDS

Stratification of common ragweed (Ambrosia artemisiifolia) seeds at 4 C was most successful for breaking dormancy, whereas -5 C was least effective and 10 C was intermediate. Germination in the light exceeded that in the dark at all stratification and germination temperatures. The optimum temperatures for germination in the light were 10/20, 15/25, and 20/30. Maximum germination in the dark occurred at 20/30 C for seeds stratified at 4 and 10 C but the optimum temperatures for seeds stratified at -5 C were 10/20, 15/25, and 20/30. Seeds stratified at -5 and 10 C germinated best after 15 weeks of stratification, whereas 12 weeks of stratification at 4 C resulted in maximum germination. Secondary dormancy was induced in seeds which did not germinate in the dark. This was affected by stratification temperature and duration and germination temperature. The ecological significance of these germination characteristics is discussed.     

SEED GERMINATION STUDIES IN MUSA. II. ALTERNATING TEMPERATURE REQUIREMENT FOR THE GERMINATION OF MUSA BALBISIANA

Stotzky , G., and Elsie A. Cox . (Central Research Labs., United Fruit Co., Norwood, Mass.) Seed germination studies in Musa. II. Alternating temperature requirement for the germination of Musa balbisiana. Amer. Jour. Bot. 49(7): 763–770. Illus. 1962.—Alternating temperatures were found to be required for the germination of seeds of Musa balbisiana. The temperature differentials optimal for germination in soil are dependent upon both the high and low temperatures, and range from 8–23 C. Germination is maximal when the seeds are held 6–12 hr at the high (27–35 C) and 12–18 hr at the low (12–18 C) temperatures. Some germination can be induced by short exposures to alternating temperatures followed by constant high temperatures, but continuous exposure to alternating temperatures is necessary for maximum germination. Excised embryos develop better at constant than at alternating temperatures, showing that the mechanisms affected by alternating temperatures reside elsewhere in the seed. Alternating temperatures are also required for germination of mechanically scarified seeds, although the temperature differentials are less than those necessary for intact seeds, indicating that the action of alternating temperatures is not on the permeability of the integuments.     

Seed germination and seedling growth ofCarex doenitzii growing on alpine zone of Mt. Fuji

Carex doenitzii on the upper timberline of Mt. Fuji were studied to determine the effect of thermal conditions on their seed germination and seedling growth. Mature seeds collected at the end of the growing season were divided into five test groups, and each was germinated at constant temperature, the temperatures being 15 C, 20 C, 25 C, 30 C and 35 C. Seed germination percentage was highest (93%) at 25 C. Seedlings germinated at 25 C were grown in chambers at 15/10 C, 25/20 C and 35/30 C. Growth of seedlings was greatest at 25/20 C. The data suggest that the seed germination and seedling growth ofC. doenitzii occur only under limited conditions in the field.     

AUTECOLOGICAL STUDIES ON THE MARINE DIATOM RHIZOSOLENIA FRAGILISSIMA BERGON. I. THE INFLUENCE OF LIGHT,TEMPERATURE, AND SALINITY1

The influence of 113 combinations of temperature (9, 12, 18, 25, 30 C), salinity (5–35 ‰ at 5 ‰ intervals), and light (4 levels) on the mean daily cell division rate (K) of the Narragansett Bay clone of Rhizosolenia fragilissima was examined following appropriate preconditioning. Growth did not occur below 9 C, but was excellent (K =～1.2) under certain combinations of light and salinity at 12, 18, and 25 C. The optimal salinity of 20–25 ‰ was temperature independent. Growth was not measurable at 5 ‰, although survival occurred. At 20 ‰ and 1200 ft-c, K increased approximately 1.8-fold from 0.65 to ～1.2 between 9 and 18–25 C. The optimal light intensity was generally 600 ft-c, although several light-temperature-salinity trends were found. At 10 ‰ at all temperatures, the mean daily division rate decreased with increasing light above 600 ft-c, a response found at all salinities at 12 C, but not at other temperatures. Between 15 and 25 ‰, at 18 and 25 C, mean growth was independent of light intensity; at 30–35 ‰ a direct relationship with light may be present with maximum growth occurring at 1200–1800 ft-c. The in situ and in vitro responses of Rhiz. fragilissima to salinity and the optimum and upper temperature levels are in general agreement. However, growth failure below 9 C in vitro is at odds with reports that natural populations occur even at ?1.11 C. The questions of to what extent this discrepancy reflects the occurrence of thermal clones, different taxa, and/or experimental artifacts are briefly discussed. It is suggested that naturally occurring populations found below 9 C might be designated as Rhiz. fragilissima f. faeröensis, and that Rhiz. fragilissima f. bergonii be used for populations growing at higher temperatures, until this matter is resolved. Observations on auxospore formation are presented.     

Effect of salinity on seed germination and seedling growth of the halophyte Suaeda japonica Makino

Seed germination and seedling growth of the annual halophyte species Suaeda japonica Makino were investigated in response to variable salinity of sediment pore water. The germination percentage of S. japonica’s soft brown seeds, which are dominant among dimorphic seeds, decreased with an increase in salinity, although germination was still observed at 1200‐mM NaCl concentration. The germination percentage and germination speed observed in April were higher than those observed in December when treated with sediment water with 400–1200 mM of NaCl concentrations. These data suggest that S. japonica seedlings could be established on sediments that experience high temperatures. Germination recovery of S. japonica seeds transferred from 600‐mM NaCl containing sediment (seawater equivalent) was lowest among 0–1200‐mM NaCl treatments, implying the low tolerance of seawater conditions of S. japonica seeds. Seeds germinated in 900‐ to 1200‐mM NaCl medium showed poor growth, but survived, in hypersaline conditions, and exhibited improvement in growth upon transfer to lower salinity.     

THE GERMINATION STRATEGY OF OLDFIELD ASTER (ASTER PILOSUS)

At maturity in November, a high percentage of Aster pilosus Willd. seeds germinated in light at high temperatures (30/15, 35/20 and 40/25 C). Stratification during winter lowered the temperature requirement for germination, and high percentages of germination were obtained in light at 15/6 and 20/10 C., as well as at 30/15, 35/20 and 40/25 C. Stratification in darkness was completely ineffective, but stratification in light was partially effective in overcoming the light requirement for germination. Inability of seeds to germinate at low temperatures prevents germination after dispersal in late autumn and winter, when freezing temperatures could kill the seedlings. The lowering of the temperature requirement for germination during winter stratification allows the seeds to germinate and the resulting vegetative rosettes to become well established before the onset of the periodic summer droughts that occur in habitats occupied by A. pilosus.     

GERMINATION ECOLOGY OF PHACELIA DUBIA VAR. DUBIA IN TENNESSEE GLADES

The germination characteristics of a population of the winter annual Phacelia dubia (L.) Trel. var. dubia from the middle Tennessee cedar glades were investigated in an attempt to define the factor(s) regulating germination in nature. Factors considered were changes in physiological response of the seeds (after-ripening), temperature, age, light and darkness, and soil moisture. At seed dispersal (late May to early June), approximately 50 % of the seeds were non-dormant but, would germinate only at low temperatures (10–15 C). As the seeds aged from June to September, there was an increase in rate and total percent of germination at 10, 15, and 20 C, and the maximum temperature for germination increased to 25 C. Little or no germination occurred at the June, July, and August temperatures in 0- to 2-month-old seeds, even in seeds on soil that was kept continuously moist during this 3-month period. At the September, October, and November temperatures 3- to 5-month-old seeds germinated to high percentages. In all experiments seeds germinated better at a 14-hr photoperiod than in constant darkness. Inability of 0- to 2-month-old seeds to germinate at high summer temperatures allows P. dubia dubia to pass the dry summer in the seed stage, while increase in optimum and maximum temperatures for germination during the summer permits seeds to germinate in late summer and early fall when conditions are favorable for seedling survival and eventual maturation.     

Light,temperature, dry after‐ripening and salt stress effects on seed germination of Phleum sardoum (Hackel) Hackel

Phleum sardoum is an endemic psammophilous species of Sardinia, growing exclusively on coastal sandy dunes. The effect of glumes on seed germination, germination requirements at constant (5–25°C) and alternating (25/10°C) temperatures, both in the light (12/12 h) and in the dark were evaluated, as well as the effect of a dry after‐ripening period (90 days at 25°C), the salt stress effect (0–600 mmol NaCl) and its recovery on seed germination. The presence of glumes reduced final germination percentages. For fresh naked seeds, high germination percentages were observed at 10°C. Dry after‐ripening increased germination rate at low temperatures, but did not affect final germination percentages. NaCl determined a secondary salt‐induced dormancy which recovery interrupted only partially. Our results highlighted that this species has its optimum of germination during autumn–winter when, under a Mediterranean climate, water availability is highest and soil salinity levels are minimal.     

Foliage colour influence on seed germination of Bienertia cycloptera in Arabian deserts

Bienertia cycloptera (Chenopodiaceae) produces two types of leaf foliage colour (reddish and yellowish). In order to determine the role of leaf colour variation in regulating the germination characteristics and salinity tolerance during germination, a study was conducted on seeds collected from plants of both colours. Seeds with and without pulp were germinated under two illumination conditions (12‐h light photoperiod and continuous dark), three alternating temperature regimes (15/25°C, 20/30°C and 25/35°C), and several salinity levels at 20/30°C. Germination percentage was significantly higher for seeds without pulp as compared to the seeds with pulp. The response of B. cycloptera seeds to salinity depended on the leaf colour. Thus, the seeds collected from reddish coloured plants were able to tolerate higher salinity compared to those of yellowish coloured plant. The germination recovery results indicate that the seeds from both coloured plants could remain viable in saline condition and they will be able to germinate once the salinity level are decreased by rain. The production of different foliage colours by B. cycloptera seems to be an adaptative strategy which increases the possibility for establishment in unpredictable environments by producing seeds with different germination requirements and salinity tolerance.     

Germination characteristics ofDiamorpha cymosa seeds and an ecological interpretation

Summary Laboratory-stored seeds ofDiamorpha cymosa (Nutt.) Britton (Crassulaceae) were germinated at monthly intervals starting shortly after maturity in late May and ending at approximately the time germination is completed in the field (November). Seeds were placed at 5, 10, 15, 20, 25, 30, 15/6, 20/10, 30/15 and 35/20°C at a 14-hr photoperiod (12/12 hr thermoperiods at the alternating temperature regimes) and in constant darkness. In June, seeds were almost completely dormant and thus germinated poorly or not at all under all conditions. As seeds aged from late May to November 1. germination at the 14-hr photoperiod increased in rate and total percentage, 2. the maximum germination temperature increased from 15 to 25°C at constant temperatures and from 20/10 to 30/15°C at the alternating temperature regimes and 3. the optimum temperature for germination increased from 15 to 15–20°C at constant temperatures but remained at20/10°C at alternating temperature regimes throughout the study. During the same period germination in constant darkness was negligible at constant and alternating temperature regimes. This pattern of physiological after-ripening apparently is an adaptation to summer-dry,winter-wet habitats such as rock outcrops of southeastern United States.A short period of illumination with white light given after a 12-hr imbibition period in darkness promoted germination in the dark at 25/10°C but not at 15 or 25°C. A short period of illumination given during the imbibition period was much less effective in promoting germination in the dark. Drying up to 7 days did not cause light-stimulated seeds to lose their ability to germinate in darkness. The light requirement for seed germination probably does not play a role in restrictingD. cymosa to its well-lighted habitats on granite and sandstone outcrops.This research was supported by funds from the University of Kentucky Research Foundation and by an NIH Biomedical Sciences Support Grant to the University of Kentucky.     

Variation in temperature and light but not salinity invokes antioxidant enzyme activities in germinating seeds of Salsola drummondii

Seeds with efficient antioxidant defence system show higher germination under stress conditions; however, such information is limited for the halophyte seeds. We therefore studied lipid peroxidation and antioxidant responses of a leaf-succulent halophyte Salsola drummondii during seed germination under different salinity levels (0, 200 and 800 mM NaCl), temperature (10/20, 20/30 and 25/35°C) and light regimes. Seeds absorbed water and germinated in less than 1 h in non-saline control while increases in salinity decreased the rate of water uptake as well as seed germination. Non-optimal temperatures (10/20 and 25/35°C) and complete dark condition reduced seed germination in comparison to those seeds germinated under optimal temperature (20/30°C) and 12-h photoperiod, respectively. Generally, higher lipid peroxidation and antioxidant enzyme activities were observed in seeds at non-optimal temperature and in those seeds germinated in dark. Decrease in reduced ascorbic acid content was found in highest salinity and temperature treatments, while reduced glutathione content did not change significantly with changes in salinity, temperature and light regimes. These results indicate variation in temperature and light but not salinity enhances antioxidant enzyme activities in germinating seeds of Salsola drummondii.     

Germination behaviour of Conyza bonariensis to constant and alternating temperatures across different populations

Conyza bonariensis is one of the most problematic weed species throughout the world. It is considered highly noxious due to its interference with human activities, and especially the competition it poses with economically important crops. This research investigated the temperature requirements for seed germination of four populations of C. bonariensis with distinct origin and the influence of daily alternating temperatures. For this, a set of germination tests were performed in growth chambers to explore the effect of constant and alternating temperatures. Seeds of the four populations (from Lleida, Badajoz and Seville, Spain and Bahía Blanca, Argentina) were maintained at constant temperatures ranging from 5 to 35°C. The final germination and cardinal temperatures (base, optimum and maximum) of each population were obtained. We also tested the influence of daily alternating temperatures on final germination. To do so, seeds were exposed to two temperature regimes: 5/15, 10/20, 15/25, 20/30 and 25/35°C night/day temperature (intervals increasing 5°C, with constant oscillation of 10°C) and to 18/22, 16/24, 14/26, 12/28 and 10/30°C night/day temperature (intervals with average of 20°C, but increasing the oscillation in 4°C between intervals). In general, all populations behaved similarly, with the highest germination percentages occurring in the optimum temperature range (between 21.7°C and 22.3°C) for both constant and alternating temperatures. In general, climatic origin affected germination response, where seeds obtained from the coldest origin exhibited the highest germination percentage at the lowest temperature assayed. In addition, we observed that the alternating temperatures can positively affect total germination, especially in oscillations that were further from the average optimum temperature (20°C), with high germination percentage for the oscillations of 15/25, 20/30, 18/22, 16/24, 14/26, 12/28 and 10/30°C in all populations. The cardinal temperatures obtained were significantly different across the populations. These results provide information that will facilitate a better understanding of the behaviour of Conyza and improve current field emergence models.     

Seed Germination and Radicle Growth of a Halophyte, Kalidium caspicum(Chenopodiaceae)

Effects of temperature, light, NaCl and polyethylene glycol(PEG)-6000 on seed germination and radicle growth in a halophyticshrub, Kalidium caspicum(L.) Ung.-Sternb. were investigated.When seeds were incubated in deionized water at constant temperaturesbetween 10 and 30°C, the percentage germination in the darkexceeded 75%; light suppressed seed germination at alternatingtemperatures. Incubating seeds with a hypersaline solution ofNaCl for 30 d had no adverse effect on their germinability.The percentage germination of seeds incubated with a –0.8MPa NaCl solution was 73, 80 and 54% at 10, 20 and 30°C,respectively, but all radicles died before their length exceeded5 mm. In contrast, when seeds were incubated with a –0.8MPa PEG solution at 20°C, 68% of seeds germinated, and 95%of the emerging radicles survived beyond 5 mm. The high sensitivityof small radicles of this species to salinity indicated thatsalt must be removed from the soil surface for seedling establishment.Copyright2000 Annals of Botany Company Chinese desert, radicle growth, germination, halophyte, Kalidium caspicum, salinity     

The performance of carrot seeds in relation to their viability

The germination and emergence characteristics, and early seedling growth, of carrot seeds cv. Chantenay red-cored from different sources with a range of germination from 54–94%, was compared. Seeds from protected crops (mean temperature of growth 21°C, r.h. 45–70%) gave higher percentage germination than those from crops grown outdoors (mean temperature 15°C, 70–100% r.h.). Germination was also higher from mature (seed moisture content at harvest 20% or lower) than immature seed (seed moisture content at harvest between 20 and 60%). High percentage germination (>90%) was associated with low mean germination times and low spreads of germination times whilst the reverse was true for low percentage germination. Similar relationships were found for seedling emergence characters in the field although a lower proportion of the viable seeds produced seedlings from slowly than rapidly germinating seed lots. In general, seed lots having a low percentage germination gave greater variability in plant weight than those of higher percentage germination. There was no effect of seed source on radicle or shoot relative growth rates or on post-emergence seedling growth rates.     

Effects of maternal salinity on salt tolerance during germination of Suaeda aegyptiaca,a facultative halophyte in the Arab Gulf desert

Suaeda aegyptiaca is a facultative halophyte found in saline and non‐saline habitats of the Arab Gulf desert, which produces small‐sized undispersible seeds. The interactive effects of maternal salinity and other environmental conditions, such as salinity, light and temperatures, that are prevailing during seed germination have received little attention for a facultative halophyte. This study tested the effects of maternal salinity on salt tolerance during seed germination of S. aegyptiaca under different light and temperature regimes. Seeds collected from both saline and non‐saline habitats of the United Arab Emirates (UAE) were germinated in 0, 50, 100, 200 and 400 mM NaCl, and incubated at 15/25°C, 20/30°C and 25/35°C in both 12‐h light/12‐h dark regimes and continuous darkness. Generally, seeds of the non‐saline habitat were 56% heavier and attained greater germination at the lower temperatures than seeds of the saline habitat. Seeds of the saline habitat germinated better in saline solutions at higher temperatures and in light. Germination was faster for seeds of the saline habitat than for seeds of non‐saline habitats. Germination recovery after transfer to distilled water was significantly greater for seeds from the non‐saline habitat, compared with seeds from saline habitats. Recovery was greater at lower and/or moderate temperatures, compared with at higher temperatures. Germination was significantly faster during recovery, compared with in the saline solutions. The study indicates that the maternal effect of salinity was confounded with the seed‐size effect and it cannot be conclusively confirmed.     

Ecophysiology of seed germination in Erythronium japonicum (Liliaceae) with underdeveloped embryos

Erythronium japonicum (Liliaceae) (Japanese name, katakuri) is indigenous to Japan and adjacent Far East regions. We examined their embryo elongation, germination, and seedling emergence in relationship to the temperature. In incubators, seeds did not germinate at 20°/10° (light 12 h/dark 12 h alternating temperature), 20°, 15°, 5°, or 0°C with a 12-h light photoperiod for 200 d. They germinated at 15°/5° or 10°C, starting on day 135. If seeds were kept at 20° or at 25°/15°C before being exposed to 5°C, the seeds germinated, but if kept at 25° or 30°C they did not. Embryos at 25°/15°C grew to half the seed length without germinating; at 0° or 5°C, embryos elongated little. Embryos grew and seeds germinated when kept at 25°/15°C for 90 d and then at 5°C. In the field, seeds are dispersed in mid-June in Hokkaido and in Honshu, mid-May to mid-June. Seeds do not germinate immediately after dispersal because the embryo is underdeveloped. Embryos elongated at medium temperatures in autumn after summer heat, and germination ends in November at 8°/0°C. After germination, seedling emergence was delayed, and most seedlings were observed in early April around the snowmelt when soil cover was 2-3 mm.     

A butenolide, isolated from smoke, can overcome the detrimental effects of extreme temperatures during tomato seed germination

The butenolide, 3-methyl-2H-furo[2, 3-c]pyran-2-one, is an highly active compound isolated from plant-derived smoke. This compound is known to stimulate seed germination in a wide range of plants akin to smoke or aqueous extracts of smoke. The present study attempted to elucidate the role of the butenolide in overcoming detrimental effects of low and high temperatures on tomato seed germination and seedling growth. The germination percentage followed a parabolic curve for temperatures ranging from 10 to 40°C, with 25°C being the optimum for all treatments. Control seeds showed radicle emergence at two extreme temperatures (10 and 40°C) and seedlings failed to develop further, even upon prolonged incubation. By comparison the butenolide-treated seeds grew into phenotypically normal seedlings at these non-optimum temperatures. The smoke–water-treated seeds had an intermediate response as only a fraction of germinated seed developed into normal seedlings. Seedling vigour indices as well as seedling weight were significantly higher (p ≤ 0.05) for butenolide-treated seeds at all temperatures. Furthermore, seedlings developed in the presence of the butenolide had about a 1:1 correspondence between root and shoot length. Butenolide-treated seeds grew better than the control seeds in the temperature shift experiments. A gradual decline in the vigour index values was recorded with an increased duration of incubation at the extreme temperatures. Results of the present study are very important from an horticultural point of view as they indicate the potential use of the butenolide compound in restoring normal seed germination and seedling establishment in tomato below and above optimum temperatures.     

THE EFFECT OF SEED DIMORPHISM ON THE GERMINATION AND SURVIVAL OF SALICORNIA EUROPAEA L. POPULATIONS

Seed dimorphism influenced the germination behavior of Salicornia europaea L., with small seeds being more dormant and less salt tolerant than large seeds. All of the large less dormant seeds of S. europaea germinated prior to May, and all seedlings produced after this time were from small seeds. A persistent seed bank was maintained by the small dormant seeds. Survivorship was relatively constant during the normal germination season, but increasing salinity stress at any time during the spring reduces the chance of seedling survival. Little germination occurred from July through September because of the high surface soil salinities during this period.     

FACTORS AFFECTING DORMANCY,GERMINATION, AND SEEDLING DEVELOPMENT OF AEGINETIA INDICA L. (OROBANCHACEAE)

Dormancy in seeds of the parasitic phanerogam Aeginetia indica L. can be broken by chemical treatment with sodium hypochlorite, which also helps to control contaminating microflora. A germination medium was developed that suppressed microbial contamination and permitted long-term observation of these slow-germinating seeds. The medium consisted of 10 ppm streptomycin, 10 ppm penicillin, and 10⁻⁵ m indole-3-acetic acid (IAA) (or other growth regulator) in 1 % water agar. Optimum germination range was 25–30 C. Dormancy could also be broken by exposure on agar for several days at 3-5 C (stratification), or by brief exposures (15 min) to 50 C. Continuous light as low as 0.1 ft-c completely inhibited germination on this growth medium. Brief, intermittent light exposures depressed germination. Germination and growth in vitro of nondormant seed of Aeginetina indica L. can be described in five stages: (1) Germination: expansion of spheroidal cells or nodule at micropylar end of the seed, stimulated by growth regulators. Unique stimulation of germination by IAA was noted; (2) Tendril formation: production of a root-hairlike protrusion in response to seedling roots or extract of pea seedlings; (3 and 4) Tendril septation and branching: induced by pea extract; (5) Seedling extension growth: cell growth and division adjacent to nodule by action of various carbohydrate-containing growth factors. This type of growth may bypass tendril formation.     

Germination responses of Diplotaxis harra to temperature and salinity

Diplotaxis harra (Forssk.) Boiss, an annual herb in the family of Brassicaceae, is widely distributed in many sandy and gypseous areas in southern Tunisia. Laboratory experiments were carried out to assess the effects of temperature and salinity on seed germination and recovery responses after seed transfer to distilled water. The germination responses of the seeds in complete darkness were determined over a wide range of temperatures (5, 10, 15, 20, 25 and 30 °C) and salinities (0, 50, 100, 150 and 200 mM NaCl). Germination was inhibited by either an increase or decrease in temperature from the optimal temperature (15 °C). Highest germination percentages were obtained under non-saline conditions and an increase in NaCl concentrations progressively inhibited seed germination. Rate of germination decreased with an increase in salinity at all temperatures but comparatively higher rates were obtained at 15 °C. Salt stress decreased both the percentage and the rate of germination. An interaction between salinity and temperature yielded no germination at 200 mM NaCl. Seeds were transferred from salt solution to distilled water after 20 days, and those from low salinities recovered at all temperatures. At NaCl concentration of 200 mM, the recovery of germination was completely inhibited.