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

2000 ◽  
Vol 78 (9) ◽  
pp. 1199-1205 ◽  
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.

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

Horticulturae ◽  
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.

Seed dormancy and germination of the subalpine geophyte Crocus alatavicus (Iridaceae)

2013 ◽  
Vol 61 (5) ◽  
pp. 376 ◽  
Author(s):  
Ziyan Fu ◽  
Dunyan Tan ◽  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Central Asia ◽  
Seed Dormancy ◽  
Natural Habitat ◽  
Early Summer ◽  
Cold Stratification ◽  
Dormancy Breaking ◽  
Morphophysiological Dormancy ◽  
Radicle Emergence ◽  
Germination Requirements ◽  
Seed Dormancy And Germination

Crocus alatavicus Regel et Sem. is a cormous perennial primarily distributed in central Asia that may have potential in horticulture; however, relatively little is known about seed dormancy in the genus Crocus. The primary aim of the present study was to identify the dormancy breaking and germination requirements of seeds of C. alatvicus and to assign them to a dormancy category. In its natural habitat, the underdeveloped embryo in C. alatavicus seeds grows in early summer, and radicles emerge in early autumn. However, cotyledon emergence is delayed until the following spring. Radicle emergence was promoted by warm stratification and cotyledon emergence by cold stratification. GA3 was ineffective in promoting either radicle or epicotyl emergence. We conclude that seeds of C. alatavicus have deep simple epicotyl morphophysiological dormancy of the type C1bB(root) – C3(shoot). To our knowledge, this is the first detailed study on the ecophysiology of seed dormancy and germination in the genus Crocus.

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

2009 ◽  
Vol 19 (2) ◽  
pp. 115-123 ◽  
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.

The great diversity in kinds of seed dormancy: a revision of the Nikolaeva–Baskin classification system for primary seed dormancy

2021 ◽  
pp. 1-29
Author(s):  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Seed Dormancy ◽  
Seed Coat ◽  
Classification System ◽  
Primary Dormancy ◽  
Morphophysiological Dormancy ◽  
Physiological Dormancy ◽  
Whole Seed ◽  
Dust Seeds ◽  
Impermeable Seed Coat ◽  
Morphological Dormancy

Abstract This review provides a revised and expanded word-formula system of whole-seed primary dormancy classification that integrates the scheme of Nikolaeva with that of Baskin and Baskin. Notable changes include the following. (1) The number of named tiers (layers) in the classification hierarchy is increased from three to seven. (2) Formulae are provided for the known kinds of dormancy. (3) Seven subclasses of class morphological dormancy are designated: ‘dust seeds’ of mycoheterotrophs, holoparasites and autotrophs; diaspores of palms; and seeds with cryptogeal germination are new to the system. (4) Level non-deep physiological dormancy (PD) has been divided into two sublevels, each containing three types, and Type 6 is new to the system. (5) Subclass epicotyl PD with two levels, each with three types, has been added to class PD. (6) Level deep (regular) PD is divided into two types. (7) The simple and complex levels of class morphophysiological dormancy (MPD) have been expanded to 12 subclasses, 24 levels and 16 types. (8) Level non-deep simple epicotyl MPD with four types is added to the system. (9) Level deep simple regular epicotyl MPD is divided into four types. (10) Level deep simple double MPD is divided into two types. (11) Seeds with a water-impermeable seed coat in which the embryo-haustorium grows after germination (Canna) has been added to the class combinational dormancy. The hierarchical division of primary seed dormancy into many distinct categories highlights its great diversity and complexity at the whole-seed level, which can be expressed most accurately by dormancy formulae.

Intermediate morphophysiological dormancy allows for life-cycle diversity in the annual weed, Turgenia latifolia (Apiaceae)

2014 ◽  
Vol 62 (8) ◽  
pp. 630 ◽  
Author(s):  
Miregul Nurulla ◽  
Carol C. Baskin ◽  
Juan J. Lu ◽  
Dun Y. Tan ◽  
Jerry M. Baskin
Keyword(s):  
Life Cycle ◽  
Low Temperatures ◽  
Western China ◽  
Intermediate Complex ◽  
Dormancy Breaking ◽  
Morphophysiological Dormancy ◽  
Temperature Regimes ◽  
Germination Phenology ◽  
Physiological Dormancy ◽  
Winter Annual

Our aim was to determine the seed dormancy-breaking requirements and type of life cycle of Turgenia latifolia in north-western China. At dispersal in July, only 0–9% of the seeds germinated at 5/2°C, 15/2°C, 20/10°C and 25/15°C; thus, 91% of the seeds exhibited physiological dormancy (PD) and 9% were non-dormant. Also, the embryo was underdeveloped and embryo length : seed length ratio increased from 0.38 in fresh seeds to 0.79 at germination. Seeds buried in dry soil at the four temperature regimes for 12 weeks germinated to ≥50% when tested in darkness at 5/2°C, and those buried at 15/2°C and 20/10°C germinated to ≥50% when tested at 15/2°C. Seeds have intermediate complex morphophysiological dormancy (MPD). PD was broken at high and/or low temperatures, but embryo growth was completed only at low temperatures; gibberellic acid (GA3) promoted germination. Seeds buried under natural conditions during summer germinated to ~70% and ~55% at 5/2°C and 15/2°C, respectively, in darkness in autumn. In a germination-phenology study, cumulative germination was ~20% and ~80% in autumn and spring, respectively. Intermediate complex MPD allows the species to behave as a winter annual and as a short-lived summer annual.

A comparative study of the seed germination biology of a narrow endemic and two geographically-widespread species ofSolidago(Asteraceae). 1. Germination phenology and effect of cold stratification on germination

1997 ◽  
Vol 7 (1) ◽  
pp. 47-58 ◽  
Author(s):  
Jeffrey L. Walck ◽  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Small Area ◽  
Geographic Range ◽  
The Other ◽  
Cold Stratification ◽  
Dormancy Breaking ◽  
Widespread Species ◽  
Narrow Endemic ◽  
Germination Phenology ◽  
Primary Difference ◽  
Germination Requirements

AbstractSolidago shortiiis endemic to a small area in northcentral Kentucky (USA), whereas two of its sympatric congeners,S. altissimaandS. nemoralis, are geographically widespread. Seeds (achenes) ofS. shortii(0.370 mg) are significantly larger (PLSD,P=0.05) than those ofS. altissima(0.070 mg) andS. nemoralis(0.068 mg). Germination percentages of freshly-matured seeds of the threeSolidagospecies collected in November 1991, 1992 and 1994 were 0–2% in light at 15/6°C, 1–37% at 20/10°C, 9–56% at 25/15°C and 10–85% at 30/15 and 35/20°C. Stratification increased the percentage and rate of germination and decreased the time to the onset of germination (measured by Timson's index only at 20/10°C in light) in the three species. Following 12 weeks of cold stratification in light, seeds of the three species germinated to 72–100% in the light and to 22–100% in darkness over the range of thermoperiods; those cold-stratified in darkness germinated to 39–100% in light. Freshly-matured seeds ofS. altissimaand ofS. nemoralisgerminated to 0–4% in darkness, whereas those cold-stratified for 12 weeks in darkness germinated to 0–28% in darkness. On the other hand, freshly-matured and cold-stratified (in darkness) seeds ofS. shortiigerminated to 0–13 and 13–73%, respectively, in darkness. Under near-natural temperatures in a glasshouse without temperature control, germination of the three species peaked in March. Thus, the primary difference in dormancy-breaking and germination requirements of the three species is that the endemic germinates to a much higher percentage in darkness than its two congeners. Seeds ofS. shortiido not have any special dormancy-breaking or germination requirements that could not be fulfilled outside its present-day geographic range.

A new type of non-deep physiological dormancy: evidence from three annual Asteraceae species in the cold deserts of Central Asia

2014 ◽  
Vol 24 (4) ◽  
pp. 301-314 ◽  
Author(s):  
Mihray Nur ◽  
Carol C. Baskin ◽  
Juan J. Lu ◽  
Dun Y. Tan ◽  
Jerry M. Baskin
Keyword(s):  
Central Asia ◽  
Mechanical Resistance ◽  
Dormancy Breaking ◽  
Germination Phenology ◽  
Physiological Dormancy ◽  
Temperature Requirements ◽  
Dry Conditions ◽  
New Type ◽  
Late Stages ◽  
Germination Requirements

AbstractAlthough Asteraceae species are important in the cold deserts of Central Asia, little is known about their seed dormancy and germination. We determined dormancy breaking and germination requirements of three annual Asteraceae, Echinops gmelinii, Epilasia acrolasia and Koelpinia linearis. Achenes (seeds) were tested for germination in light and in darkness over a range of alternating temperatures after various periods of burial outdoors and of dry storage. Germination phenology was monitored for seeds sown in irrigated and non-irrigated sand, and temperature requirements for dormancy break were determined under wet and dry conditions. Effects of pericarp and phyllaries on germination of E. acrolasia and E. gmelinii, respectively, were determined. Low percentages of 20-day-old seeds of E. acrolasia and K. linearis were non-dormant and germinated to low percentages over the range of temperatures, whereas all seeds of E. gmelinii were dormant. As seeds of the three species afterripened, they germinated over the range of temperatures. Whether seeds germinated in autumn or spring depended on the amount of sand moisture. Mechanical resistance of the pericarp and phyllaries reduced germination of E. acrolasia and E. gmelinii, respectively. Temperature requirements for germination as seeds come out of dormancy do not correspond to any of the known five types of non-deep physiological dormancy (PD). Thus, a sixth type is recognized in which germination occurs over the same range of temperatures in the early and late stages of dormancy break. Type 6 allows seeds to germinate at high or at low temperatures, whenever sand moisture is non-limiting.

scholarly journals Seed Germination Biology of Four Pomegranate (Punica granatum) Cultivars from Xinjiang, China

HortScience ◽  
2015 ◽  
Vol 50 (6) ◽  
pp. 826-829 ◽  
Author(s):  
Dilinuer Shalimu ◽  
Ke Li ◽  
Carol C. Baskin ◽  
Jerry M. Baskin ◽  
Yujun Liu
Keyword(s):  
Sulfuric Acid ◽  
Seed Germination ◽  
Punica Granatum ◽  
Poor Quality ◽  
Cold Stratification ◽  
Dormancy Breaking ◽  
Physiological Dormancy ◽  
Pomegranate Seeds ◽  
Germination Requirements ◽  
New Cultivars

Pomegranate is an important fruit crop cultivated in many countries, and development of new cultivars depends on the plant breeders being able to produce plants from seeds. Poor quality and low yield of cultivars are widespread problems that greatly restrict development of the pomegranate industry. Our purpose was to gain a better understanding of the seed dormancy-breaking and germination requirements of four cultivars of pomegranate from Xinjiang Province, China, which would be useful in improving old cultivars and developing new ones. Fresh pomegranate seeds incubated on moist filter paper imbibed water, but they germinated to only 16% to 20%. Sulfuric acid scarification, cold stratification, and warm followed by cold stratification significantly increased germination percentages. Seeds soaked in concentrated H2SO4 for 40 minutes followed by cold stratification for 2 months germinated to 65%, and those warm stratified for 1–3 months followed by cold stratification for 2 months germinated to 75% to 80%. Seeds of pomegranate have nondeep physiological dormancy (PD).

Multiple environmental signals required for embryo growth and germination of seeds of Selinum carvifolia (L.) L. and Angelica sylvestris L. (Apiaceae)

2007 ◽  
Vol 17 (4) ◽  
pp. 283-291 ◽  
Author(s):  
Filip Vandelook ◽  
Nele Bolle ◽  
Jozef A. Van Assche
Keyword(s):  
Seedling Emergence ◽  
Early Spring ◽  
Time Interval ◽  
Short Time Interval ◽  
Cold Stratification ◽  
Dormancy Breaking ◽  
Environmental Signals ◽  
Morphophysiological Dormancy ◽  
Physiological Dormancy ◽  
Short Time

AbstractGermination and dormancy breaking requirements were studied in Selinum carvifolia (L.) L. and Angelica sylvestris L. (Apiaceae). Seeds of these two species have an underdeveloped embryo and are morpho-physiologically dormant. The embryo does not start to grow until physiological dormancy is broken by cold stratification. Incubating seeds at fluctuating temperatures in the light, after cold stratification, had a stimulating effect on embryo growth and seed germination. Seeds of S. carvifolia and A. sylvestris have non-deep simple morphophysiological dormancy (MPD), since gibberellic acid (GA3) could substitute for cold stratification. This is the first report of non-deep simple MPD that is broken by cold stratification in the Apiaceae. Under natural conditions, physiological dormancy is broken by low temperature conditions during winter. Embryo growth and germination occur in a short time interval when temperatures start rising in early spring. Due to the fact that multiple environmental signals regulate dormancy, seedling emergence in these species is timed very accurately in spring.

Dormancy-breaking and germination requirements of seeds of fourLoniceraspecies (Caprifoliaceae) with underdeveloped spatulate embryos

2000 ◽  
Vol 10 (4) ◽  
pp. 459-469 ◽  
Author(s):  
Siti N. Hidayati ◽  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Soil Surface ◽  
The Other ◽  
Cold Stratification ◽  
Dormancy Breaking ◽  
Morphophysiological Dormancy ◽  
Seed Maturity ◽  
Breaking Dormancy ◽  
Natural Temperature ◽  
To Come ◽  
Germination Requirements

AbstractDormancy-breaking requirements and types of dormancy were determined for seeds ofLonicera fragrantissimaLindl. & Paxt.,L. japonicaThunb.,L. maackii(Rupr.) Maxim. andL. morrowiiA. Gray. Seeds of all four species have underdeveloped spatulate embryos that are about 20–40%fully developed (elongated) when dispersed. Embryos in freshly matured, intact seeds grew better at 25/15°C than at 5°C. Gibberellic acid (GA3) (tested only in the light) was more effective in breaking dormancy inL. maackiiandL. morrowiithan inL. fragrantissimaandL. japonica. Warm- followed by cold stratification was required to break dormancy in seeds ofL. fragrantissima, whereas seeds ofL. japonicarequired cold stratification only. Thus, seeds ofL. fragrantissimahave deep simple morphophysiological dormancy (MPD) and those ofL. japonicanondeep simple MPD. About 50%of the seeds ofL. maackiirequired warm- or cold stratification only to come out of dormancy and 50% of those ofL. morrowiirequired warm stratification only, whereas the other 50% did not require stratification to germinate. Thus, about half of the seeds of the two species has nondeep simple MPD, and the other half has morphological dormancy (MD). In these laboratory tests, seeds ofL. japonica,L. maackii, andL. morrowiigenerally germinated to significantly higher percentages in light than in darkness; seeds ofL. fragrantissimawere not tested in darkness. Peaks of germination for seeds ofL. fragrantissima,L. japonica,L. maackiiandL. morrowiisown on a soil surface and covered withQuercusleaves under near-natural temperature conditions shortly after seed maturity and dispersal in late June 1997, late November 1997, early November 1996 and late June 1998, respectively, occurred in early March 1998, late February 1998, late March 1997 and early October 1998, respectively. The germination phenologies of seeds of the same species and seed lots buried in soil were similar to those of seeds under leaf litter. High percentages of seeds of all four species germinated both under litter (78–96%) and beneath the soil surface (78–97%). These germination patterns correspond closely with the requirements for embryo growth and dormancy break in the fourLoniceraspecies.

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