Seed Dormancy Class and Ecophysiological Features of Veronicastrum sibiricum (L.) Pennell (Scrophulariaceae) Native to the Korea Peninsula

Veronicastrum sibiricum is a perennial species distributed in Korea, Japan, Manchuria, China, and Siberia. This study aimed to determine the requirements for germination and dormancy break of V. sibiricum seeds and to classify the kind of seed dormancy. Additionally, its class of dormancy was compared with other Veronicastrum and Veronica species. V. sibiricum seeds were permeable to water and had a mature embryo during seed dispersal. In field conditions, germination was prevented by physiological dormancy, which was, however, relieved by March of the next year, allowing the start of germination when suitable environmental conditions occurred. In laboratory experiments, the seeds treated with 0, 2, 4, 8, and 12 weeks of cold stratification (4 °C) germinated to 0, 79, 75, 72, and 66%, respectively. After the GA3 treatment (2.887 mM), ≥90% of the seeds germinated during the four incubation weeks at 20/10 °C. Thus, 2.887 mM GA3 and at least two weeks at 4 °C were effective in breaking physiological dormancy and initiating germination. Therefore, the V. sibiricum seeds showed non-deep physiological dormancy (PD). Previous research, which determined seed dormancy classes, revealed that Veronica taxa have PD, morphological (MD), or morphophysiological seed dormancy (MPD). The differences in the seed dormancy classes in the Veronicastrum-Veronica clade suggested that seed dormancy traits had diverged. The results provide important data for the evolutionary ecological studies of seed dormancy and seed-based mass propagation of V. sibiricum.

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Practical Methods for Breaking Seed Dormancy in a Wild Ornamental Tulip Species Tulipa thianschanica Regel

Agronomy ◽

10.3390/agronomy10111765 ◽

2020 ◽

Vol 10 (11) ◽

pp. 1765

Author(s):

Wei Zhang ◽

Lian-Wei Qu ◽

Jun Zhao ◽

Li Xue ◽

Han-Ping Dai ◽

...

Keyword(s):

Seed Germination ◽

Seed Dormancy ◽

Combined Treatment ◽

Individual Treatment ◽

Cold Stratification ◽

Slight Effect ◽

Sowing Depth ◽

Physiological Dormancy ◽

Commercial Breeding ◽

Breaking Seed Dormancy

The innate physiological dormancy of Tulipa thianschanica seeds ensures its survival and regeneration in the natural environment. However, the low percentage of germination restricts the establishment of its population and commercial breeding. To develop effective ways to break dormancy and improve germination, some important factors of seed germination of T. thianschanica were tested, including temperature, gibberellin (GA3) and/or kinetin (KT), cold stratification and sowing depth. The percentage of germination was as high as 80.7% at a constant temperature of 4 °C, followed by 55.6% at a fluctuating temperature of 4/16 °C, and almost no seeds germinated at 16 °C, 20 °C and 16/20 °C. Treatment with exogenous GA3 significantly improved the germination of seeds, but KT had a slight effect on the germination of T. thianschanica seeds. The combined treatment of GA3 and KT was more effective at enhancing seed germination than any individual treatment, and the optimal hormone concentration for the germination of T. thianschanica seeds was 100 mg/L GA3 + 10 mg/L KT. In addition, it took at least 20 days of cold stratification to break the seed dormancy of T. thianschanica. The emergence of T. thianschanica seedlings was the highest with 82.4% at a sowing depth of 1.5 cm, and it decreased significantly at a depth of >3.0 cm. This study provides information on methods to break dormancy and promote the germination of T. thianschanica seeds.

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Non-Deep Physiological Dormancy in Seed and Germination Requirements of Lysimachia coreana Nakai

Horticulturae ◽

10.3390/horticulturae7110490 ◽

2021 ◽

Vol 7 (11) ◽

pp. 490

Author(s):

Saeng Geul Baek ◽

Jin Hyun Im ◽

Myeong Ja Kwak ◽

Cho Hee Park ◽

Mi Hyun Lee ◽

...

Keyword(s):

Seed Germination ◽

Seed Dormancy ◽

Germination Rate ◽

Seed Viability ◽

Cold Stratification ◽

Dormancy Breaking ◽

Viability Test ◽

Physiological Dormancy ◽

Different Temperatures ◽

Germination Requirements

This study aimed to determine the type of seed dormancy and to identify a suitable method of dormancy-breaking for an efficient seed viability test of Lysimachia coreana Nakai. To confirm the effect of gibberellic acid (GA3) on seed germination at different temperatures, germination tests were conducted at 5, 15, 20, 25, 20/10, and 25/15 °C (12/12 h, light/dark), using 1% agar with 100, 250, and 500 mg·L−1 GA3. Seeds were also stratified at 5 and 25/15 °C for 6 and 9 weeks, respectively, and then germinated at the same temperature. Seeds treated with GA3 demonstrated an increased germination rate (GR) at all temperatures except 5 °C. The highest GR was 82.0% at 25/15 °C and 250 mg·L−1 GA3 (4.8 times higher than the control (14.0%)). Additionally, GR increased after cold stratification, whereas seeds did not germinate after warm stratification at all temperatures. After cold stratification, the highest GR was 56.0% at 25/15 °C, which was lower than the GR observed after GA3 treatment. We hypothesized that L. coreana seeds have a non-deep physiological dormancy and concluded that 250 mg·L−1 GA3 treatment is more effective than cold stratification (9 weeks) for L. coreana seed-dormancy-breaking.

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Cool–Warm Temperature Stratification and Simulated Bird Digestion Optimize Removal of Dormancy in Rosa rugosa Seeds

Frontiers in Plant Science ◽

10.3389/fpls.2021.808206 ◽

2022 ◽

Vol 12 ◽

Author(s):

Peng Gao ◽

Jie Dong ◽

Sihan Wang ◽

Wuhua Zhang ◽

Tao Yang ◽

...

Keyword(s):

Water Absorption ◽

Seed Dormancy ◽

Global Climate ◽

Natural Populations ◽

Suitable Condition ◽

Growth Potential ◽

Cold Stratification ◽

Rosa Rugosa ◽

Physiological Dormancy ◽

Mechanical Constraint

Rosa rugosa Thunb. has been explored multi-function in medicinal, edible, cosmetic, ornamental and ecological etc. However, R. rugosa natural populations have recently declined substantially in China, besides of global climate change, this species also has the defect of limiting the reproduction of itself such as the hard-to-release seed dormancy. In this study, only 30% of R. rugosa seeds were viable, and the others were incompletely developed or diseased seeds. Without stratification, morphologically complete viable seeds imbibed water but those seeds could not germinate even after seed husk removal under suitable condition to exhibit a physiological dormancy. After cold (4°C) and warm (18 ± 2°C) stratification, macromolecular substances containing carbon or nitrogen accumulated, and respiration, antioxidant enzyme activity, and gibberellin (GA3) /abscisic acid (ABA) and auxin (IAA)/ABA ratios increased significantly in seeds. Water absorption also increased as endocarps softened. Thus, physiological dormancy of seed was broken. Although warm and cold stratification increased separation between endocarp and embryo, the endocarp binding force was removed insufficiently, because only 10.20% of seeds germinated. Therefore, stratified seeds were treated with simulated bird digestion. Then, folds and cracks in loosened endocarps increased permeability, and water absorption rate increased to 64.43% compare to 21.14% in cold and warm stratification treatment. With simulated digestion, 24.20% of radicles broke through the endocarp with plumules and cambiums to develop into seedlings. Thus, the seed dormancy type of R. rugosa is physiological as seeds imbibed water and possessed fully developed embryos with a low growth potential in combination with a mechanical constraint from the endocarp. Cold stratification helped remove physiological dormancy, and additional warm stratification accelerated the process. The optimal stratification treatment was 4°C for 45 days followed by 18 ± 2°C for 15 days. After warm and cold stratification, simulated bird digestion broke the mechanical constraint from the seed covering layers. Based on this research, production of R. rugosa seedlings can be greatly increased to help protect the species from further declines.

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Germination of drupelets in multi-seeded drupes of the shrub Leptecophylla tameiameiae (Ericaceae) from Hawaii: a case for deep physiological dormancy broken by high temperatures

Seed Science Research ◽

10.1079/ssr2005223 ◽

2005 ◽

Vol 15 (4) ◽

pp. 349-356 ◽

Cited By ~ 19

Author(s):

Carol C. Baskin ◽

Jerry M. Baskin ◽

Alvin Yoshinaga ◽

Ken Thompson

Keyword(s):

Gibberellic Acid ◽

Seed Dormancy ◽

Cold Stratification ◽

Long Period ◽

Subtype B ◽

Physiological Dormancy ◽

To Come ◽

Subtype A ◽

Number Of Seeds ◽

Excised Embryos

This study addressed the difficulty of germinating drupelets (hereafter seeds) in the multi-seeded stony dispersal units (drupes) of Leptecophylla tameiameiae (Ericaceae). Embryos in fresh seeds were 77% the length of the endosperm, and seeds inside the intact drupes imbibed water. We monitored germination at 15/6, 20/10 and 25/15°C for 162 weeks, after which each drupe was cut open and ungerminated seeds counted. Drupes contained 1–6 seeds, and the total number of seeds in all treatments and controls was 1977, with 20, 29, 25, 18, 7 and <1% of them occurring in one-, two-, three-, four-, five- and six-seeded drupes, respectively. The percentage of seeds germinating in one-, two-, three-, four-, five- and six-seeded drupes was 74, 66, 65, 72, 56 and 0, respectively. Neither warm nor cold stratification for 6 or 12 weeks significantly increased germination percentages, compared to controls incubated continuously at 25/15°C for 162 weeks, where 72% of the seeds in the drupes germinated. At 25/15°C, 24–49 weeks were required for 20% of the seeds to germinate. Warm followed by cold stratification did not promote germination, and there was no widening of the temperature range for germination. Like seeds of other species known to have deep physiological dormancy (PD), those of L. tameiameiae required extended periods of time (16 to ≥162 weeks) to come out of dormancy and germinate, gibberellic acid (GA3) did not promote germination and excised embryos failed to grow. Thus, we conclude that seeds of L. tameiameiae have deep PD. However, unlike seeds of other species with deep PD, those of L. tameiameiae required an extensive period of warm rather than of cold stratification to come out of dormancy. It is suggested that a subtype a (seeds require a long period of cold stratification to come out of dormancy) and a subtype b (seeds require a long period of exposure to warm stratification to come out of dormancy) of deep PD be recognized in the Nikolaeva formula system for classifying seed dormancy.

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Non-deep physiological dormancy in seeds of Euphorbia jolkinii Boiss. native to Korea

Journal of Ecology and Environment ◽

10.1186/s41610-021-00194-x ◽

2021 ◽

Vol 45 (1) ◽

Author(s):

Hye Jin Oh ◽

Un Seop Shin ◽

Seung Youn Lee ◽

Sang Yong Kim ◽

Mi Jin Jeong

Keyword(s):

Gibberellic Acid ◽

Seed Dormancy ◽

Coastal Area ◽

Jeju Island ◽

Perennial Species ◽

Physiological Dormancy ◽

Different Temperatures ◽

Number Of Seeds ◽

Seed Dormancy And Germination

Abstract Background Euphorbia jolkinii Boiss. is a perennial species native to Jeju Island and the southern coastal area of Korea. Particularly on Jeju Island, the yellow flowers of E. jolkinii Boiss. have a high ornamental value because of their contrast with basalt. This study was conducted to investigate the effects of different temperatures (5, 15, 20, and 25 °C) and gibberellic acid (GA3) concentrations (0, 10, 100, or 1000 mg/L) on seed dormancy and germination of E. jolkinii. In addition, we classified the seed dormancy type and compared types with those of other species in the same genus. Results The number of seeds with viable embryos and endosperms was approximately 66%. The final germination percentages at 5, 15, 20, and 25 °C were 51.7%, 83.5%, 2.6%, and 0.0%, respectively. In GA3 concentration experiments, the final germination percentages of 0, 10, 100, and 1000 mg/L were 83.5%, 91.7%, 79.1%, and 83.4%, respectively, at 15 °C conditions, and 0.0%, 6.9%, 13.2%, and 27.3%, respectively, at 25 °C. Conclusions Germination improved at temperatures of 15 °C or lower. Furthermore, GA3 treatment effectively reduced germination times. Thus, the seeds of E. jolkinni were classified as having non-deep physiological dormancy.

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Dormancy-breaking and germination requirements for seeds of Diervilla lonicera (Caprifoliaceae), a species with underdeveloped linear embryos

Canadian Journal of Botany ◽

10.1139/b00-094 ◽

2000 ◽

Vol 78 (9) ◽

pp. 1199-1205 ◽

Cited By ~ 5

Author(s):

Siti N Hidayati ◽

Jerry M Baskin ◽

Carol C Baskin

Keyword(s):

Seed Dormancy ◽

Constant Darkness ◽

Cold Stratification ◽

Dormancy Breaking ◽

Morphophysiological Dormancy ◽

Germination Phenology ◽

Physiological Dormancy ◽

Temperature Controlled ◽

Germination Requirements ◽

Morphological Dormancy

Dormancy-breaking requirements and type of dormancy were determined for seeds of Diervilla lonicera Mill. Seeds have an underdeveloped linear embryo that is about 35% of the length of the seed at maturity. Embryos (in intact seeds) grew at 25:15°C but not at 5°C. Up to 85% of the freshly matured seeds had morphological dormancy (MD), and thus, they germinated within about 30 days on a moist substrate in light at 30:15°C; a maximum of 3% of the seeds germinated in constant darkness. The other portion of fresh seeds had nondeep simple morphophysiological dormancy (MPD) and required a period of warm stratification or treatment with GA3 to break dormancy. These seeds also required light to germinate. In contrast, cold stratification induced dormancy, and dry storage for up to 1 year did not effectively break dormancy. Seeds with MD germinated to significantly higher percentages on soil than on filter paper or on sand. Seeds sown on soil in a non-temperature-controlled greenhouse in mid-November germinated mostly in late May, whereas those sown in mid-April germinated in early May. Apparently, embryos of November-sown seeds were induced into physiological dormancy during winter. Thus, seeds had MPD in spring and needed several weeks of warm temperatures for dormancy break, embryo growth, and germination. This is the first report on seed dormancy in the genus Diervilla.Key words: embryo growth, germination phenology, Diervilla lonicera, morphological seed dormancy, morphophysiological seed dormancy, underdeveloped linear embryo.

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Seed Dormancy and Soil Seed Bank of the Two Alpine Primula Species in the Hengduan Mountains of Southwest China

Frontiers in Plant Science ◽

10.3389/fpls.2021.582536 ◽

2021 ◽

Vol 12 ◽

Author(s):

De-Li Peng ◽

Li-E Yang ◽

Juan Yang ◽

Zhi-Min Li

Keyword(s):

Seed Dormancy ◽

Seed Bank ◽

Southwest China ◽

Soil Seed Bank ◽

Cold Stratification ◽

Hengduan Mountains ◽

Dormancy Release ◽

Physiological Dormancy ◽

Alpine Environments ◽

Seed Dormancy And Germination

The timing of germination has long been recognized as a key seedling survival strategy for plants in highly variable alpine environments. Seed dormancy and germination mechanisms are important factors that determining the timing of germination. To gain an understanding of how these mechanisms help to synchronize the germination event to the beginning of the growing season in two of the most popular Primula species (P. secundiflora and P. sikkimensis) in the Hengduan Mountains, Southwest China, we explored their seed dormancy and germination characteristics in the laboratory and their soil seed bank type in the field. Germination was first tested using fresh seeds at two alternating temperatures (15/5 and 25/15°C) and five constant temperatures (5, 10, 15, 20, and 25°C) in light and dark, and again after dry after-ripening at room temperature for 6 months. Germination tests were also conducted at a range of temperatures (5–30, 25/15, and 15/5°C) in light and dark for seeds dry cold stored at 4°C for 4 years, after which they were incubated under the above-mentioned incubation conditions after different periods (4 and 8 weeks) of cold stratification. Base temperatures (Tb) and thermal times for 50% germination (θ50) were calculated. Seeds were buried at the collection site to test persistence in the soil for 5 years. Dry storage improved germination significantly, as compared with fresh seeds, suggesting after-ripening released physiological dormancy (PD); however, it was not sufficient to break dormancy. Cold stratification released PD completely after dry storage, increasing final germination, and widening the temperature range from medium to both high and low; moreover, the Tb and θ50 for germination decreased. Fresh seeds had a light requirement for germination, facilitating formation of a persistent soil seed bank. Although the requirement reduced during treatments for dormancy release or at lower alternating temperatures (15/5°C), a high proportion of viable seeds did not germinate even after 5 years of burial, showing that the seeds of these two species could cycle back to dormancy if the conditions were unfavorable during spring. In this study, fresh seeds of the two Primula species exhibited type 3 non-deep physiological dormancy and required light for germination. After dormancy release, they had a low thermal requirement for germination control, as well as rapid seed germination in spring and at/near the soil surface from the soil seed bank. Such dormancy and germination mechanisms reflect a germination strategy of these two Primula species, adapted to the same alpine environments.

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Regulation of Seed Dormancy and Germination Mechanisms in a Changing Environment

International Journal of Molecular Sciences ◽

10.3390/ijms22031357 ◽

2021 ◽

Vol 22 (3) ◽

pp. 1357

Author(s):

Ewelina A. Klupczyńska ◽

Tomasz A. Pawłowski

Keyword(s):

Climate Change ◽

Seed Germination ◽

Seed Dormancy ◽

Environmental Conditions ◽

Global Climate ◽

Plant Evolution ◽

Suitable Habitat ◽

Climate Change Scenarios ◽

Adaptation Mechanism ◽

Seed Dormancy And Germination

Environmental conditions are the basis of plant reproduction and are the critical factors controlling seed dormancy and germination. Global climate change is currently affecting environmental conditions and changing the reproduction of plants from seeds. Disturbances in germination will cause disturbances in the diversity of plant communities. Models developed for climate change scenarios show that some species will face a significant decrease in suitable habitat area. Dormancy is an adaptive mechanism that affects the probability of survival of a species. The ability of seeds of many plant species to survive until dormancy recedes and meet the requirements for germination is an adaptive strategy that can act as a buffer against the negative effects of environmental heterogeneity. The influence of temperature and humidity on seed dormancy status underlines the need to understand how changing environmental conditions will affect seed germination patterns. Knowledge of these processes is important for understanding plant evolution and adaptation to changes in the habitat. The network of genes controlling seed dormancy under the influence of environmental conditions is not fully characterized. Integrating research techniques from different disciplines of biology could aid understanding of the mechanisms of the processes controlling seed germination. Transcriptomics, proteomics, epigenetics, and other fields provide researchers with new opportunities to understand the many processes of plant life. This paper focuses on presenting the adaptation mechanism of seed dormancy and germination to the various environments, with emphasis on their prospective roles in adaptation to the changing climate.

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Morphological and physiological dormancy in seeds of Aegopodium podagraria (Apiaceae) broken successively during cold stratification

Seed Science Research ◽

10.1017/s0960258509301075 ◽

2009 ◽

Vol 19 (2) ◽

pp. 115-123 ◽

Cited By ~ 14

Author(s):

Filip Vandelook ◽

Nele Bolle ◽

Jozef A. Van Assche

Keyword(s):

Low Temperature ◽

Seedling Emergence ◽

Early Spring ◽

Temperate Climate ◽

Cold Stratification ◽

Dormancy Breaking ◽

Morphophysiological Dormancy ◽

Temperature Requirement ◽

Physiological Dormancy ◽

Chilling Period

AbstractA low-temperature requirement for dormancy break has been observed frequently in temperate-climate Apiaceae species, resulting in spring emergence of seedlings. A series of experiments was performed to identify dormancy-breaking requirements of Aegopodium podagraria, a nitrophilous perennial growing mainly in mildly shaded places. In natural conditions, the embryos in seeds of A. podagraria grow in early winter. Seedlings were first observed in early spring and seedling emergence peaked in March and April. Experiments using temperature-controlled incubators revealed that embryos in seeds of A. podagraria grow only at low temperatures (5°C), irrespective of a pretreatment at higher temperatures. Seeds did not germinate immediately after embryo growth was completed, instead an additional cold stratification period was required to break dormancy completely. Once dormancy was broken, seeds germinated at a range of temperatures. Addition of gibberellic acid (GA3) had a positive effect on embryo growth in seeds incubated at 10°C and at 23°C, but it did not promote germination. Since seeds of A. podagraria have a low-temperature requirement for embryo growth and require an additional chilling period after completion of embryo growth, they exhibit characteristics of deep complex morphophysiological dormancy.

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Sensitivity cycling and its ecological role in seeds with physical dormancy

Seed Science Research ◽

10.1017/s096025850818730x ◽

2009 ◽

Vol 19 (1) ◽

pp. 3-13 ◽

Cited By ~ 29

Author(s):

K.M.G. Gehan Jayasuriya ◽

Jerry M. Baskin ◽

Carol C. Baskin

Keyword(s):

Life Cycle ◽

Environmental Conditions ◽

Common Phenomenon ◽

Ecological Role ◽

Dormancy Breaking ◽

Physical Dormancy ◽

Physiological Dormancy ◽

Seed Coats

AbstractCycling of physically dormant (PY) seeds between states insensitive and sensitive to dormancy-breaking factors in the environment has recently been demonstrated inFabaceaeandConvolvulaceae, and it may be a common phenomenon in seeds with water-impermeable seed coats. In contrast to seeds of many species with physiological dormancy (PD), those with PY cannot cycle between dormancy and non-dormancy (ND). In this paper, we evaluate the role of sensitivity cycling in controlling the timing of germination of seeds with PY in nature, and show that sensitivity cycling in seeds with PY serves the same ecological role as dormancy cycling in seeds with PD. Thus, sensitivity cycling in seeds with PY ensures that germination in nature occurs only at (a) time(s) of the year when environmental conditions for growth are, and are likely to remain, suitable long enough for the plant to complete its life cycle or to form a perennating structure. Further, we describe the experimental procedures necessary to determine whether sensitivity cycling is occurring, and discuss briefly the possible relevance of sensitivity cycling to dormancy classification.

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