Seed germination ecology of poison hemlock, Conium maculatum

1990 ◽  
Vol 68 (9) ◽  
pp. 2018-2024 ◽  
Author(s):  
Jerry M. Baskin ◽  
Carol C. Baskin
Keyword(s):  
Late Winter ◽  
Cold Stratification ◽  
North Central ◽  
Conium Maculatum ◽  
Morphophysiological Dormancy ◽  
Key Words Dispersal ◽  
Embryo Dormancy ◽  
Monocarpic Perennial ◽  
Autumn And Winter ◽  
Morphological Dormancy

In north-central Kentucky, United States, seeds of Conium maculatum are dispersed from mid-September to mid to late February, with up to 95% of them being dispersed by late December. Depending on the year, 40–85% of the freshly matured seeds had morphological dormancy (MD) and thus needed only a moist substrate, 10–15 14-h photoperiod days and 12-h alternating thermoperiods of 30:15 °C for embryo growth and germination. The other seeds had morphophysiological dormancy (MPD), and embryo dormancy had to be broken before embryo growth and germination could occur. MPD was broken in some of the undispersed seeds during summer, and by September 50–85% (depending on the year) germinated at 25:15 °C in light. During late autumn and winter, 35–95% (depending on the year) of the undispersed seeds in MD in autumn entered MPD. Cold stratification at 5 °C induced about half the seeds with MD into MPD. Seeds in MD germinated to higher percentages on soil than on sand, and in light than in darkness. Most of the seeds sown on soil in a nonheated greenhouse in July, August, and September germinated in September. Seeds sown in October and November germinated in autumn, late winter, and the following autumn, and those sown in late winter germinated in spring and autumn. The later seeds were sown, the higher germination percentages were the following autumn. Key words: dispersal, dormancy, germination, morphological dormancy, poison hemlock, Conium maculatum, monocarpic perennial.

Underdeveloped embryos and kinds of dormancy in seeds of two gymnosperms: Podocarpus costalis and Nageia nagi (Podocarpaceae)

2013 ◽  
Vol 23 (1) ◽  
pp. 75-81 ◽  
Author(s):  
Shun-Ying Chen ◽  
Carol C. Baskin ◽  
Jerry M. Baskin ◽  
Ching-Te Chien
Keyword(s):  
Seed Plants ◽  
Cold Stratification ◽  
Morphophysiological Dormancy ◽  
Seed Maturity ◽  
Basal Clade ◽  
Radicle Emergence ◽  
Primitive Condition ◽  
Morphological Dormancy

AbstractAlthough it has been speculated that seeds of the gymnosperm family Podocarpaceae have an underdeveloped embryo, no detailed studies have been done to definitively answer this question. Our purpose was to determine if embryos in seeds of two species of Podocarpaceae, Podocarpus costalis and Nageia nagi, from Taiwan are underdeveloped and to examine the kind of dormancy the seeds have. Embryos in fresh seeds of P. costalis were 4.6 ± 0.5 mm long, and they increased in length by about 54% before radicle emergence (germination), demonstrating that the embryo is underdeveloped at seed maturity. Seeds germinated to >90% at 30/20, 25/15 and 25°C in light in ≤ 4 weeks, without any cold stratification pretreatment. Thus, seeds of P. costalis have morphological dormancy (MD). Embryos in fresh seeds of N. nagi were 7.4 ± 0.8 mm long and they increased in length by about 39% before radicle emergence (germination) occurred, indicating that the embryo is underdeveloped at seed maturity. Seeds germinated to < 25% at 30/20 and 25°C in light in 4 weeks but to >90% at the same temperatures in 12 weeks. Thus, most seeds of N. nagi have morphophysiological dormancy (MPD). Although underdeveloped embryos are considered to be a primitive condition in seed plants, they also occur in the most advanced orders. The occurrence of underdeveloped embryos in Podocarpaceae documents that they are not restricted to a basal clade in gymnosperms.

scholarly journals Different levels of morphophysiological seed dormancy in Ribes alpinum and R. uva-crispa (Grossulariaceae) facilitate adaptation to differentiated habitats

2020 ◽  
Vol 29 (2) ◽  
pp. e017
Author(s):  
Raquel Herranz-Ferrer ◽  
Miguel Ángel Copete-Carreño ◽  
José María Herranz-Sanz ◽  
Elena Copete-Carreño ◽  
Pablo Ferrandis-Gotor
Keyword(s):  
Seed Dormancy ◽  
Seedling Emergence ◽  
Late Summer ◽  
Late Winter ◽  
Minimal Size ◽  
Morphophysiological Dormancy ◽  
Radicle Emergence ◽  
Embryo Length ◽  
Different Levels ◽  
Morphological Dormancy

Aim of the study: To study the germination ecology of two species of the genus Ribes to reveal their levels of morphophysiological dormancy (MPD) and to facilitate the production of plants from seeds, a key tool for population reinforcement.Area of study: Experiments were carried out both outdoors and in the laboratory in Albacete (Spain) with seeds from the Meridional Iberian System mountain range.Material and methods: Seeds from one population of Ribes alpinum and from other of Ribes uva-crispa were collected during several years. Embryo length, radicle and seedling emergence, and effects on germination of stratification and GA3 were analysed to determine the level of MPD.Main results: In R. alpinum, embryo length in fresh seeds was 0.49 mm, needing to grow to 1.30 mm to germinate. Warm stratification (25/10ºC) promoted embryo length enlargement to 0.97 mm. Afterwards, seeds germinated within a wide temperature range. Embryo growth and seedling emergence occur late summer-early autumn. In R. uva-crispa, embryo length in fresh seeds was 0.52 mm, being 2.10 mm the minimal size to germinate. Embryos exposed to a moderately warm stratification (20/7ºC + 15/4ºC) followed by cold (5ºC) grew to 2.30 mm. Then, seeds germinated ≥ 80% when incubated at temperatures ≥ 15/4ºC. Embryos grew in autumn/early winter, and seedlings emerged late winter-early spring.Research highlights: These results showed that R. alpinum seeds have a nondeep simple MPD while R. uva-crispa seeds have a nondeep complex MPD. Moreover, the different germinative models found for each species help explain their installation in distinct habitats.Keywords: Ribes; seed dormancy break; radicle emergence; seedling emergence; nondeep simple and nondeep complex MPD.Abbreviations used: Morphophysiological dormancy (MPD), morphological dormancy (MD), Gibberellic acid (GA3), months (m).

scholarly journals Seed dormancy and germination in Cardiocrinum giganteum var. yunnanense, a perennial herb in China with post-dispersal embryo growth

2020 ◽  
Vol 48 (2) ◽  
pp. 303-314
Author(s):  
Ye-Fang Li ◽  
Jie Song ◽  
Wen-Ling Guan ◽  
Feng-Rong Li
Keyword(s):  
Seed Germination ◽  
Seed Dormancy ◽  
Practical Knowledge ◽  
Perennial Herb ◽  
Late Winter ◽  
Dormancy Breaking ◽  
Morphophysiological Dormancy ◽  
Summer Temperatures ◽  
Autumn And Winter ◽  
Seed Dormancy And Germination

Seeds of Cardiocrinum giganteum var. yunnanense, which is native to China, has underdeveloped embryos when dispersed from parent plants that did not grow until the second autumn and winter after exposure to summer temperatures. Radicles and cotyledons emerged in late winter and spring. Thus, a 15–16 month period was required from dispersal to seed germination. Under laboratory conditions, this period could be shortened to 5–6 months in a 25°C/15°C (60 days) → 15°C/5°C (60 days) → 5°C (60 days) temperature sequence. Based on dormancy-breaking requirements, the seeds have deep simple morphophysiological dormancy (MPD). This is practical knowledge for propagation of the species from seeds.

Seeds of Thalictrum mirabile (Ranunculaceae) require cold stratification for loss of nondeep simple morphophysiological dormancy

2000 ◽  
Vol 77 (12) ◽  
pp. 1769-1776 ◽  
Author(s):  
Jeffrey L Walck ◽  
Carol C Baskin ◽  
Jerry M Baskin
Keyword(s):  
Gibberellic Acid ◽  
Seed Bank ◽  
Soil Seed Bank ◽  
Early Spring ◽  
Late Winter ◽  
Cold Stratification ◽  
Morphophysiological Dormancy ◽  
Physiological Dormancy ◽  
Buried Seeds ◽  
Persistent Soil Seed Bank

Seeds of the eastern North American herbaceous polycarpic perennial Thalictrum mirabile Small have differentiated but underdeveloped (small) embryos that are physiologically dormant at maturity in September. Physiological dormancy was broken effectively by cold stratification at 1°C, but embryos required temperatures [Formula: see text]15:6°C for growth after physiological dormancy was broken. Gibberellic acid substituted for cold stratification. Breaking of physiological dormancy in seeds exposed to natural temperatures in a greenhouse occurred during winter, and embryo growth and germination occurred in late winter - early spring. Furthermore, seeds in the greenhouse remained viable until the second and third (spring) germination seasons. Thus, T. mirabile seeds have the capacity to form a short-lived persistent soil seed bank. Buried seeds of T. mirabile apparently go through an annual dormancy-nondormancy cycle. Seeds buried in September 1994 were nondormant when exhumed in April 1995 and April 1996 and incubated in light at 25:15°C for 2 weeks, but they were dormant in June 1995 and September 1995. Seeds of T. mirabile have nondeep simple morphophysiogical dormancy. This is the first report of nondeep simple morphophysiological dormancy being broken by cold, and not by warm, stratification.

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.

Taiwanese montaneSambucus chinensisseeds require warm stratification, contrasting with other congeneric temperate members

2014 ◽  
Vol 24 (3) ◽  
pp. 217-228 ◽  
Author(s):  
Shun-Ying Chen ◽  
Ching-Te Chien ◽  
Siti N. Hidayati ◽  
Jeffrey L. Walck
Keyword(s):  
North America ◽  
Cold Stratification ◽  
Cold Temperatures ◽  
Tropical Regions ◽  
Morphophysiological Dormancy ◽  
Primary Mechanism ◽  
Northern Latitudes ◽  
Northern Hemispheric ◽  
Response To Temperature ◽  
Seed Characteristics

AbstractMany temperate plant genera, likeSambucus, have species with range disjunctions among North America, Europe and/or Asia. Cold stratification (sometimes in combination with warm stratification) is the primary mechanism to break seed dormancy in these species. For some of these genera showing Northern Hemispheric disjunctions, members also occur in subtropical or tropical regions, mostly confined to higher elevations where climate and vegetation differ from those in northern latitudes. We made two hypotheses concerning germination for the subtropical TaiwaneseSambucus chinensis: (1) seeds from populations exposed to warm temperatures would require warm stratification, and (2) seeds from populations exposed to cold temperatures need cold stratification. We investigated the germination (including embryo growth) of non-stratified seeds over a range of temperatures and tested the effects of cold stratification and of gibberellins GA3and GA4on germination. The amount and timing of germination among populations varied substantially in response to temperature treatments. Seeds from all populations of this species required warm temperatures for dormancy break and germination, regardless of environmental conditions. As such, the majority of seeds had non-deep simple morphophysiological dormancy, which, until now, has not been reported in any members ofSambucus. The seed characteristics of the subtropicalS. chinensisare different from those of temperate members of the genus in which cold stratification is the predominate treatment to overcome dormancy.

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.

Dormancy of apple embryos. Are starch and reserve protein changes related to dormancy breaking?

1984 ◽  
Vol 62 (11) ◽  
pp. 2308-2315 ◽  
Author(s):  
Michelle Bouvier-Durand ◽  
Alina Dawidowicz-Grzegorzewska ◽  
Claudine Thévenot ◽  
Daniel Come
Keyword(s):  
Cold Treatment ◽  
Moderate Temperature ◽  
The Other ◽  
Cold Stratification ◽  
Dormancy Release ◽  
Dormancy Breaking ◽  
Germination Process ◽  
Embryo Dormancy ◽  
Reserve Protein ◽  
Apple Seeds

During cold stratification of apple seeds both dormancy removal and initiation of the germination process occur. To characterize these two processes and to dissociate them from each other, two different cold treatments were used. One of them (cold treatment within the fruits) excluded the germination process, the other corresponded to classical stratification. Control treatments at moderate temperature were also applied. Starch accumulated in the radicle during breaking of embryo dormancy by stratification, whereas it disappeared when dormancy was broken inside the fruits. The comparison of starch changes at 0 and at 20 °C also showed that these changes cannot be related to dormancy release. Moreover, no proteolysis occurred whether dormancy was broken or not. Proteolysis observed during stratification of the embryos seemed to be linked to their imbibition (the first step of the germination). These data refute previous observations on this problem; they demonstrate that neither starch variations nor reserve protein changes can be related to breaking of embryo dormancy.

Germination of Viburnum odoratissimum seeds: a new level of morphophysiological dormancy

2008 ◽  
Vol 18 (3) ◽  
pp. 179-184 ◽  
Author(s):  
Carol C. Baskin ◽  
Ching-Te Chien ◽  
Shun-Ying Chen ◽  
Jerry M. Baskin
Keyword(s):  
Incubation Temperature ◽  
Cold Stratification ◽  
Morphophysiological Dormancy ◽  
Physiological Dormancy ◽  
Radicle Emergence ◽  
Viburnum Odoratissimum

AbstractPrevious studies indicated that seeds of Viburnum odoratissimum had only physiological dormancy (PD), but no measurements of embryos were made during the dormancy-break treatments. Thus, we investigated embryo growth and radicle and cotyledon emergence over a range of temperatures. Seeds have underdeveloped embryos, and their length increased about 300% before radicle emergence. Embryos also had PD, as evidenced by delays in beginning of embryo growth (2–3 weeks) and of germination after embryos were elongated (4 weeks). After radicle emergence, epicotyl emergence was delayed 1–8 weeks, depending on incubation temperature, but cold stratification was not required to break PD of the epicotyl. Unlike seeds of many previously studied Viburnum spp., epicotyls of V. odoratissimum have non-deep, rather than deep, PD. Hence, a new level of MPD called non-deep, simple, epicotyl MPD has been identified.

Seed yield and hardseededness of two amphicarpic pasture legumes (Vicia sativa ssp. amphicarpa and Lathyrus ciliolatus) and two annual medics (Medicago rigidula and M. noeana)

1996 ◽  
Vol 126 (4) ◽  
pp. 421-427 ◽  
Author(s):  
S. Christiansen ◽  
A. M. Abd El Moneim ◽  
P. S. Cocks ◽  
M. Singh
Keyword(s):  
Seed Yield ◽  
Extended Period ◽  
Vicia Sativa ◽  
Pasture Legumes ◽  
Embryo Dormancy ◽  
Medicago Rigidula ◽  
Annual Medics ◽  
Total Seed ◽  
Seed Yields ◽  
Autumn And Winter

SUMMARYYields and hardseed breakdown of underground and aerial seeds in subterranean vetch (Vicia sativa ssp. amphicarpa) and lathyrus (Lathyrus ciliolatus) and aerial seeds of Medicago rigidula and M. noeana were compared at Tel Hadya, near Aleppo, in north Syria between 1990 and 1992. Underground and aerial seed and straw (mature herbage) yields were measured at maturity in the first spring, and hardseed breakdown over the following summer, autumn and winter. Regenerating herbage production was measured in the second spring.In the establishment year (292 mm rainfall) the medics produced twice as much straw as the amphicarpic species. In contrast, seed yields were less than half: M. rigidula and M. noeana produced 412 and 110 kg/ha respectively, while subterranean vetch and lathyrus produced 1174 and 736 kg/ha. More than 95 % of the total seed yield of the amphicarpic legumes was underground. Underground seeds of the amphicarpic legumes were larger than aerial seeds, and almost 10 times as large as the medic seeds.Seeds of all species were > 90% hard when newly set in summer. At the first seasonal rains > 95% of underground seed had softened, compared with 5 and 40% of the aerial seeds of vetch and lathyrus respectively. The medics remained > 90% hardseeded. In laboratory tests, embryo dormancy was observed in all species prior to the onset of first seasonal rains. For the amphicarpic legumes, but not for the medics, embryo dormancy persisted into winter. In the field, and after all germination events, 900–1430 seeds/m2 of subterranean vetch seed remained in the soil. This was considerably more than expected, based on the low levels of hardseededness and embryo dormancy observed in the laboratory. The results suggest that dormant seeds of the amphicarpic legumes need light to germinate.In the second year (353 mm rainfall), regenerating M. rigidula produced 5·3 t/ha compared with 3·4 t/ha by the best subterranean vetch from approximately equal numbers of seedlings. The amphicarpic legumes germinated later and over a more extended period than the medics, indicating that they could become weeds in a cereal/pasture rotation. However, the results suggest that in drier areas or in drier years the vetches will compare favourably with the medics in most respects. Clearly, subterranean vetch and lathyrus have great potential for pasture improvement in dry areas.

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