Seed dormancy in bay laurel (Laurus nobilis L.)

The germination of bay laurel (Laurus nobilis L.) seeds wasexamined both in the laboratory and in the field during twoyears. Seeds were collected from a grove in a garden in the townof Drama, Northern Greece, by mid November in the first year andby late November in the second year. The seeds with and withoutpericarp were given a warm-moist (20 °C day/12 °C night) oncold-moist (4±1 °C) treatment in peat or sand. After treatment theseeds were placed in the germinator along with controls. Thegermination of seeds with and without pericarp was alsoinvestigated in the field (late fall sowing). It was found thatthe pericarp caused dormancy. In seeds without pericarp,cold-moist and warm-moist stratification both proved to besuccessful in breaking embryo dormancy (100% and 96% successrespectively). The required stratification duration was 50 daysfor the warm-moist and 60 days for the cold-moist treatments.During the cold-moist stratification no germination was observed.On the other hand, seeds started to germinate during thewarm-moist stratification by about the 50th day. In the fallsowing germination was 20% for seeds with pericarp and 41% for seeds without pericarp. Drying bay laurel seeds caused areduction of the seed germination.     

Effects of tallowtree seed coat on seed germination

We measured physiological parameters including water uptake, in-vitro embryo germination ratio, and seed coat structure observed by scanning electron microscopy (SEM) to explore the influence of seed coat on the germination of seeds of tallow tree (Sapium sebiferum (Linn) Roxb.). Tallow tree seeds had good water permeability. We found that germination of cabbage seeds was inhibited when cabbage seeds were soaked in extracted solutions from tallow tree seed coat. Seed coat structure at the side of the radicle appeared to be a barrier to seed germination. We tested methods to break tallow tree seed dormancy. Dormancy of tallow tree seeds was overcome by soaking the seeds in 500 mg·L-1 or 1000 mg·L-1 GA3, followed by 100 days of cold stratification.     

Variation in germination character of Robinia pseudoacacia L. (Leguminosae) seeds at individual tree level

To demonstrate the seed dormancy and germination characters of Robinia pseudoacacia L., an exotic tall tree species in Japan, we applied scarification, cold stratification, diurnal thermal regime, heat shock, and/or winter weathering treatments to the seeds. These characters differed markedly among three seed sources (Trees K, B, and I). Scarification revealed that most seeds from Tree K showed physical dormancy, whereas those from Tree B had no physical dormancy. The seeds from Tree I showed weak physical dormancy so that the seeds eventually germinate without any treatments as time goes by. The physical dormancy in Tree K was broken by a long, high heat shock treatment. The results imply that seeds from Tree K respond to fire in natural conditions. Seeds from Tree I responded to a wide range of thermal regimes, except for long, high heat shock. In contrast, most seeds from Tree B absorbed water during cold stratification and some germinated. However, many seeds from Tree B died in the soil during the winter, presumably because of microbial and fungal infections. Seeds from Trees I and B acquired physical dormancy by weathering during the winter, implying that seedpods that remain in the crown function as an aerial seed bank. R. pseudoacacia may be able to produce various levels in dormancy with respect to the winter condition.     

Seedling growth and establishment in natural stands of yellow-cedar (Chamaecyparis nootkatensis) seedlings derived from the use of modified seed dormancy-breaking treatments

Following dispersal from the parent tree, seeds of yellow-cedar (Chamaecyparis nootkatensis[D. Don] Spach) exhibit low germination, primarily as a result of coat-imposed dormancy. Dormancy of the mature (intact) seed is effectively terminated by traditional warm/cold treatments. A chemical treatment using the anaesthetic 1-propanol combined with a three day warm water soak (30 °C), a two day GA₃ treatment and 60 d of moist chilling not only promotes high germinability of yellow-cedar seeds, but also elicits vigorous post-germinative growth following seedling emergence under nursery greenhouse conditions. Here we compare the effectiveness of the more traditional warm/cold treatments with the chemical treatment in terms of their capacity to elicit vigorous growth and establishment in natural stands following transplant of seedlings from a nursery greenhouse environment. Two seed lots (42313 and 43697) and open-pollinated seed from parent trees 13-6 and 19-8 showed equivalent seedling growth in natural stands following the chemical treatment and two traditional warm/cold treatments typically used for dormancy breakage by the forest industry and by the Ministry of Forests in British Columbia. The chemical protocol offers the advantage of reducing the time required to break seed dormancy. We have now demonstrated that it yields seedlings that exhibit vigorous growth and are capable of withstanding the vagaries of the environment.     

林木种子休眠研究评述

种子休眠,是指在充分满足各种发芽条件时,有生命力的种子一时不能发芽或发芽困难的自然现象。处于休眠的种子,种皮坚硬、含水量低,细胞内养分处于难溶态,代谢活动较低。一般将种子休眠划分为三个类型:即强迫休眠、生理休眠和综合休眠。种子生理休眠的机理包括:种果皮的抑制;植物激素的作用;种子的二次休眠;综合因素造成的休眠;分子变化等方面。     

Variations in seed germination of Hippophae salicifolia with different presoaking treatments

Mature seeds of H. salicifolia, collected from five provenances (i.e. Hanuman Chatti, Helang, Lata, Rambara and Janggal Chatti) in west Himalaya, India, were treated with stratification (at 4°C for 15, 30 and 60 days) and in different concentrations of GA₃ (5, 10, 20 mM), KNO₃ (50, 100, 200 mM) and Thiourea (50, 100, 200 mM) solution to determine the variations in seed germination. Results reveal that the germination rates of seeds from different provenances under different pre-sowing treatments are significantly increased compared to those in control (24%–30%). The seeds treated with Thiourea (100 mM) have highest germination rate (76%–83% for different seed sources), followed by those (63%–71% for different seed sources) pretreated with stratification (4°C, 30 days). GA3 treatment significantly shortens the mean germination time (MGT) and improves seed germination percentage. Considering the practical applicability and cost effectiveness, thiourea (100 mM) and stratification (at 4°C) treatments for seed germination are recommended for mass multiplication through seeds of H. salicifolia in village/forest nurseries of the west Himalaya, India.     

Optimal germination condition by sulfuric acid pretreatment to improve seed germination of Sabina vulgaris Ant.

Understanding the germination traits of plants is important not only for understanding natural regeneration processes but also for developing seedling production techniques for planting. Sabina vulgaris Ant. is a common species used for reforestation in semi-arid areas of the Mu-Us Desert, in Inner Mongolia, China, but its extremely low germination rate, both in situ and in vivo, is a bottleneck for seedling production. Sulfuric acid pretreatment was applied to improve germination, and the germination rate was compared for different soaking time (10, 30, 60, 90, and 120 min), different temperatures (10, 15, 20, 30, and 35°C) and under different lighting conditions (dark and light). Sulfuric acid treatment gave a high germination rate, reaching 60% at 30 days after sowing. However, the non-treated seeds produced no germination. The optimal treatment time in sulfuric acid was 120 min. Germination after sulfuric acid treatment increased at incubation temperatures from 10 to 30°C, but decreased at 35°C. Incubation at 25–30°C gave maximum germination of more than 50%. Light treatment had little effect on germination. Pretreatment with sulfuric acid improved water absorption by the embryo by creating cracks and cavities in the seed coat tissue. These results indicated that S. vulgaris seeds have physical dormancy caused by their hard seed coats, which prevents absorption of water into the embryo. A combination of pretreatment with sulfuric acid and incubation at 25–30°C was most effective in improving the germination of S. vulgaris seeds.     

Primary metabolite mobilization and hormonal regulation during seed dormancy release in Cornus japonica var. chinensis

The combination of gibberellin acid (GA) soaking with moist chilling plays a pivotal role in seed dormancy breaking. However, knowledge involving physiological and biochemical mechanisms for such a response is limited. This work focused on the effects of GA₃ and moist chilling on overcoming seed dormancy as well as the response of endogenous hormones and nutrient reserves to dormancy release in Chinese dogwood (Cornus kousa var. chinensis). Seeds subjected to GA₃ soaking and moist chilling exhibited a high germination percentage (average 97%), and the combination of 500 mg·L^?1 GA₃ soaking for 3 days followed with moist chilling for 50 days was more effective than other treatments. For GA₃ treatments, lipids were initially hydrolyzed during the first stage of moist chilling (0–20 days), resulting in the increase of starch and soluble sugars, while proteins were kept relatively stable. During the second stage (20–50 days), contents of lipids, starch, soluble sugars, and proteins decreased by 46%, 82%, 61% and 59%, respectively. Abscisic acid (ABA) contents and ratios of ABA to GA₃ in GA₃ treatments decreased by nearly 70% and over 90%, respectively, when dormancy was terminated. However, endogenous GA₃ contents in all treatments significantly increased with prolonged moist chilling. The present results provide insight into the metabolic mechanism involving hormonal regulation and mobilization of reserves during the release of seed dormancy in Chinese dogwood.     

Germination traits and adaptive regeneration strategies of the threeCarpinus species

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

华中樱桃种子生物学特性研究初探

为探究华中樱桃 Cerasus conradinae种子生物学特性,以 湖北省赤壁市的野生华中樱桃的自然成熟未落地的果实为试验 材料,观察其种子形态,并测定种子长度、宽度、厚度、千粒 重、吸水特性和发芽特性。结果表明：华中樱桃种子为卵形,长 7.64±0.73mm,宽5.28±0.55mm,厚4.39±0.47mm,千粒重 62.77±2.91g,属中粒种子;种子浸种0~4 h吸水较快,后渐趋 缓,浸种24 h近饱和,吸水率为33.23%,种子饱和状态时吸水率 为33.30%;用750 mg/L 赤霉素（GA3）溶液浸种处理的种子发芽 效果较清水浸种好,但差异不明显,两者发芽率分别为65.3%和 62.7%;华中樱桃幼苗个体间差异大。     

Rapid predictions of cold tolerance in Douglas-fir seedlings using chlorophyll fluorescence after freezing

Chlorophyll fluorescence measurements were performed on the foliage of 3-year-old (11/2+11/2) nursery-grown Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco] seedlings after exposure to controlled freezing temperatures, in the laboratory, to assess low temperature tolerance. The seedlings were propagated in an Irish nursery and lifted at monthly intervals overwinter 1999 and 1999–2000. Excised shoots from first-order laterals were frozen, in the dark. After freezing, needles were immediately assessed using chlorophyll fluorescence. The excised shoots were then maintained under controlled conditions for 14 days and visually assessed for needle damage. The chlorophyll fluorescence parameter, F _v/F _m, accurately predicted cold hardiness and was linearly related to visual needle damage and short-term survival. An equation was constructed using F _v/F _m data for determining the LT₅₀, that is, the freeze temperature causing 50% seedling damage. The predictions of F.LT₅₀ (fluorescence-based empirical determination of LT₅₀) have been tested over two seasons (i.e., against a second independent data set) with variability between 0 and 1.8°C of visual estimates, though predictions were often 1.1°C of the visual assessment. This approach provided a simple, rapid and accurate prediction of cold tolerance, under climatic conditions where in situ measurements are unreliable. The method can be used to predict if Douglas-fir seedlings have developed sufficient tolerance for lifting to the cold-store, or for planting.     

Effect of seed coverings and seed pretreatments on the germination response of <Emphasis Type="Italic">Alnus glutinosa</Emphasis> and <Emphasis Type="Italic">Betula pubescens</Emphasis> seeds

The germination of common alder (Alnus glutinosa (L.) Gaertn.) and downey birch (Betula pubescens Ehrh.) seeds is often poor in bare-root nurseries. The effect of a variety of seed coverings and a few seed pretreatments on seedling emergence was examined in this study in an attempt to address this problem. Seeds of each species were sown in trays containing nursery soil, covered with grit, gravel, sand, combinations of these coverings, a hydromulch or a sealed plastic cloche and then incubated for 6 weeks at 17–20°C. The grit combined with sand or gravel, the hydromulch and the cloche increased seedling emergence when compared with the standard grit. In another experiment, seeds of each species were fully imbibed (FI) (>50% moisture content, MC), as per standard practice, or adjusted to target MC (TMC) (30–35% MC) levels, and then chilled to release dormancy. Some seeds of each MC treatment were primed at 20°C for 2 days following chilling, after which all seeds were evaluated in laboratory tests and a nursery trial. Germination potential of the FI seeds declined in the lab tests by the second test date, which was reflected in low seedling emergence in the nursery in birch. The primed FI seeds of alder germinated most rapidly in the nursery, but other effects were not significant. Seedling emergence was better in the nursery in response to the TMC than the FI pretreatment in birch.

Promotion of germination of coniferous seeds by snow stratification combined with dehydration-rehydration treatment

Five chemical and four non-chemical presowing treatments were tested on seeds of three conifers (Larix principis-rupprechtii Mayr, Pinus sylvestris L. var. mongolica Litv, and Pinus tabulaeformis Carr.). By itself, cold stratification with snow for 60 days did not significantly improve the germination percentage over that of soaking the seed in warm water (45 °C) for 12 hours. However, including either one or two dehydration-rehydration cycles after the cold stratification did improve both the percentage and speed of germination of seed from all three species. Soaking seed for 12 hours in various chemicals (KNO₃, CaCl₂, CuSO₄, KMnO₄ and GA₃) before germination was less effective than the snow stratification followed by double dehydration-rehydration treatments (Chang and Lin, 1989).     

Enhancement of seed germination in Macaranga peltata for use in tropical forest restoration

We used pre-sowing treatments v/z., soaking seeds in concen- trated sulphudc acid （CSA）, gibberellic acid （GA）, combined treatment of CSA ＋ GA and mechanical scarification to overcome seed dormancy and enhance synchronous germination of Macaranga peltata seeds. We analysed percent seed germination data by logistic regression and con- finned that except in GA treatment, time and acid concentration together were crucial for enhancing germination. The combination treatment of CSA and GA resulted in higher percent germination （up to 74%） than either treatment used separately, but produced defective seedlings （26%）. Mechanical scarification of seed coat had the greatest impact in enhanc- ing germination （78%） and reducing imbibition time （6 days） against the control （0%）. Germination studies and SEM analysis confirmed that seed germination in M. peltata was inhibited by seed coat dormancy.     

Physical attributes as indicator of seed maturity and germination enhancement in Himalayan Wild Cherry (<Emphasis Type="Italic">Prunus cerasoides</Emphasis> D. Don.)

Prunus cerasoides has poor regeneration in its natural habitat due to its hard seed coat. The information about maturity time of fruit/seed is scanty and studies on seed germination enhancement lacking. In the present study, the main focus has been given to the physical fruits/seeds attributes which are reliable indicators of maturity and seed pretreatments which help to enhance germination. The fruits/seeds were collected from low and high elevational sites covering the altitudinal range of the species during the period of fruit/seed development (last week of February–mid April) for two consecutive years (2003–2004). The change in fruit colour from dark green to pale red or red was a useful indicator of seed maturity in P. cerasoides. Fruit moisture content between 46.57 ± 0.45% and 56.81 ± 1.14% and seed moisture content between 29.8 ± 1.35% and 34.13 ± 1.50% coincided with maximum germination (41.11 ± 13.96% and 59.99 ± 12.05%) across sites. The removal of seed coat (mechanical treatment) enhanced the germination of seeds to 70 ± 0% at low elevation and 100 ± 0% at high elevation in comparison of control or untreated seeds (germination range between 5.83 ± 0.83% and 31.68 ± 25.02%). Positive correlation existed between seed size and germination (r = 0.280; P < 0.01).     

Desiccation and storage behavior of bay laurel (Laurus nobilis L.) seeds

The effect of seed moisture content (m.c.) and seed storage conditions of bay laurel (Laurus nobilis L.) was investigated in relation to seed viability. In the first experiment, the effect of drying rate on seed moisture and seed germination was investigated. Fresh seeds, with their original moisture content displayed a germination percentage of 55.1%. When the seed moisture content was reduced by 2.0% in an oven, the germination percentage rose to 81.0%. When the seed moisture content was reduced even more by using the same method, the germination percentages decreased dramatically. Reducing the seed moisture content to 28.7 and 23.5% by drying the seeds in alternating room conditions resulted in an increase of seed germinability to 84.3 and 90.9%, respectively. The drying of the seeds for 45, 60 and 75 days reduced their seed germination to 66.8, 49.4 and 48.0%, respectively. Reducing seed moisture content below 15.0% resulted in practically nullifying seed germinability. The fact that bay laurel seeds cannot retain their germinability at lower moisture contents demonstrates that it is a species with recalcitrant seeds. In the second experiment, moist and dry storage conditions were tested under different temperatures and moisture contents. The storage experiment showed that the most effective way of conserving the bay laurel seeds is moist storage at 0 ± 1°C for 4 months without previous drying of the seeds.     

Mechanical but not physical dormancy is a cause of poor germination in teak (Tectona grandis L.f.)

Poor seed germination is a significant problem for propagation of teak and it particularly hampers the deployment of genetically improved material into plantations. Seed dormancy is the putative cause for delayed and sporadic germination of teak seed but specific dormancy mechanisms have not been proven. In this paper we investigate whether physical or mechanical dormancy could affect teak germination. Physical dormancy was disproved when we observed water in every examined locule of fruit which had been immersed for 12–24 h (n = 1,700 fruits from six diverse sources). Mechanical dormancy was found to affect teak seed germination by means of valve structures which must open for the radicle to emerge. All 1,450 germinating seeds in 16 samples emerged from the endocarp via the detachment of a valve. Germination over 16 days was compared between extracted seeds (ex situ) and seeds within their endocarp (in situ) to determine the effect of mechanical dormancy on germination. Significantly greater germination of the ex situ seeds (62 ± 2% SE; n = 486) than of the in situ seeds (32 ± 2% SE; n = 564) indicated that mechanical dormancy is an important factor in the poor germination of teak.     

Roles of gibberellins and abscisic acid in dormancy and germination of red bayberry (Myrica rubra) seeds

Intact seeds from freshly harvested fruits of Myrica rubra (Sieb et Zucc.) were dormant and required 8 weeks of warm stratification followed by 12 weeks of cold stratification for germination. Exogenous application of gibberellic acid (GA(3)) to intact fresh seeds was effective in breaking dormancy, with > 70% of seeds germinating when treated with 5.2 mM GA(3) and incubated at a day/night temperature of 30/20 degrees C for 20 weeks. Removing the hard endocarp or endocarp plus seed coat of fresh seeds promoted germination, and addition of GA(3) to the embryo accelerated germination. The gibberellins GA(1) and GA(4) were more effective than GA(3) in promoting germination of seeds with the endocarp removed. Endogenous contents of GA(1), GA(3), GA(4), GA(7) and GA(20) were quantified by gas chromatography-mass spectrometry-selected ion monitoring in the endocarps, seed coats and embryos of fresh seeds treated with 5.2 mM GA(3). The content of GA(3) decreased in the endocarp during incubation, whereas GA(1) contents increased in the endocarp and seed coat. A high GA(1) content was detected in the endocarps and embryos of newly germinated seeds. We speculate that GA(3) was converted to GA(1) during incubation and that GA(1) is involved in seed germination. Endogenous abscisic acid (ABA) contents were measured in fresh seeds and in warm and cold stratified seeds. The ABA content in fresh seeds was distributed in the order endocarp > seed coat > embryo, with the content in the endocarp being about 132-fold higher than in the seed coat and embryo. Total ABA content of seeds subjected to warm or cold stratification, or both, was 8.7- to 14.0-fold lower than that of fresh seeds. Low contents of endogenous GA(1), GA(3), GA(7) and GA(20), but elevated contents of GA(4), were found in the seed coats and endocarps of warm plus cold stratified seeds and in the seed coats and embryos of newly germinated seeds. These observations, coupled with the finding that GA stimulated germination of dormant Myrica seeds, provide evidence that endogenous ABA inhibited release of dormancy and that endogenous gibberellins, especially GA(4) or GA(1), or both, are involved in germination.     

Effects of osmopriming and hydropriming on vigour and germination of China aster (Callistephus chinensis (L.) Nees.) seeds

The aim of this research was to evaluate the effects of osmopriming and different hydropriming treatments on the vigour and germination of China aster (Callistephus chinensis) seeds. Seed vigour and germination tests were conducted at 10, 20 and 30°C in darkness for untreated, osmoprimed and hydroprimed seeds. The following parameters and categories of seeds and seedlings were evaluated: the mean germination time (MGT), T10, T50, U75–25, U90–10, the percentage of germinating seeds (Gmax), germination capacity, percentage of abnormal seedlings and dead seeds. The results showed that osmopriming accelerated seed germination to the largest extent and improved the uniformity of germination at 10 and 30°C. Among the hydropriming treatments the highest speed of germination was observed for seeds hydrated in 500 μL of water per 1 g of seeds for 48 h at 15°C. This treatment accelerated seed germination at 10°C compared with the control. Osmopriming increased seed germination capacity at 30°C. None of the applied hydropriming treatments improved this parameter.     

Some biological interactions between the parasitoid <Emphasis Type="Italic">Anagyrus pseudococci</Emphasis> (Girault) (Hymenoptera: Encyrtidae) and its host <Emphasis Type="Italic">Planococcus ficus</Emphasis> (Signoret) (Hemiptera: Coccoidea: Pseudococcidae)

The development, longevity, fecundity and life-table parameters of the endoparasitoid Anagyrus pseudococci (Girault) (Hymenoptera: Encyrtidae), 15 d.o. (3rd-instar nymphs) and 21 d.o. (young adult females) of the vine mealybug, Planococcus ficus (Signoret) (Hemiptera: Pseudococcidae) at 28 ± 1°C, 65 ± 10%RH and 16:8h L:D under laboratory conditions. The developmental time of female parasitoids within the host was 17.7 ± 0.39 days in 15 d.o. and 16.65 ± 0.25 days in 21 d.o. hosts; for males, development time was 16.85 ± 0.29 and 15.25 ± 0.09 days, respectively. The average number of offspring per female was 22.35 ± 1.68 in 15 d.o. and 34.8 ± 2.56 in 21 d.o. vine mealybugs. The longevity of female parasitoids was 14.8 ± 0.98 days in 15 d.o. and 15.65 ± 0.92 days in 21 d.o. mealybugs, respectively; for males, longevity was determined as 7.3 ± 0.43 and 6.7 ± 0.54 days, respectively. The mean time of pupation was 7.85 ± 0.003 days in 15 d.o. mealybugs and 8.65 ± 0.003 days in 21 d.o. mealybugs. The aggregate encapsulation rate in the parasitized 15 d.o. mealybugs was 49.73 and 60.36% in 21 d.o. mealybugs. Furthermore, effective encapsulation was 24.82% in 15 d.o. mealybugs and 37.50% in 21 d.o. mealybugs. Population growth rate (r _m) for A. pseudococci was 0.0999 female/female/days in 15 d.o. mealybugs and 0.1269 female/female/days in 21 d.o. mealybugs. The mean population generation time was 23.49 days for parasitoids reared in 15-days-old and 22.39 days when reared in 21 d.o. mealybugs.