CHANGE IN DORMANCY STATUS OF FRASERA CAROLINIENSIS SEEDS DURING OVERWINTERING ON PARENT PLANT

Seeds of the monocarpic perennial Frasera caroliniensis ripen in late summer, and most of them are dispersed in late autumn and winter. However, some viable seeds may remain undispersed for more than a year. Embryos are underdeveloped (ca. 1.1–1.3 mm long) at seed maturity and do not grow while seeds remain on plants in the field. Dormancy in freshlymatured seeds was broken by 12 to 14 weeks of cold stratification at 5 C, during which the embryos elongated. On the other hand, seeds collected in January and March required a period of warm stratification followed by a period of cold stratification to germinate. Seeds collected in September and sown in a nonheated greenhouse germinated to 83% the first spring after maturation, whereas those collected and sown in January and March did not germinate until the second spring. Thus, seeds that remained on plants in the field until winter entered a deepened state of dormancy, and a warm (summer) followed by a cold (winter) stratification period was required to overcome it.     

DORMANCY FACTORS IN IRIS (IRIDACEAE) SEEDS

Utilizing a newly developed radish seed bioassay, it has been demonstrated that Iris seed dormancy is caused by water-soluble inhibitor(s). Leached Iris seeds germinate freely when planted in soil without previous chilling. The inhibitor(s) can prevent germination of representative species of both monocotyledonous and dicotyledonous seeds.     

NONDEEP COMPLEX MORPHOPHYSIOLOGICAL DORMANCY IN SEEDS OF OSMORHIZA CLAYTONII (APIACEAE)

Freshly matured seeds of Osmorhiza claytonii exhibit a type of morphophysiological dormancy (MPD). Under natural conditions, embryo growth begins in late September and early October and continues until mid***- to late February, with the peak in October and November. Most seeds germinate between mid-February and late March. Embryos did not grow in seeds incubated for 24 weeks at 30/15 (warm stratification) or 5 C (cold stratification). However, in seeds given 12 weeks at 30/15 and then 12 weeks at 5 C, embryo length increased 1,246% while seeds were at 5 C. Zero to 7 days of warm followed by 24 weeks of cold stratification resulted in 2%–27% germination of fresh seeds, whereas 2 to 12 weeks of warm followed by 24 weeks of cold stratification resulted in 80%–98% germination. Warm plus cold stratification was required for embryo growth and germination of seeds that remained undispersed for a year in the field. GA₃ was partially effective in substituting for warm stratification. The name “nondeep complex MPD” is proposed for the type of MPD found in O. claytonii and a few other species, making a total of eight types of MPD presently known.     

DORMANCY AND GERMINATION OF COMMON RAGWEED SEEDS IN THE FIELD

Common ragweed (Ambrosia artemisiifolia) seeds were stored under natural environmental conditions by placing them at three soil levels (surface, 5 cm, and 15 cm) in the field on November 1, 1972. Germination tests at 4-week intervals indicated that dormancy was broken by the end of January. Germination was initially greater at high temperatures, but this difference decreased with increasing time in the field. Secondary dormancy was evident in surface seeds by March 21 but not until April 18 at 5 cm and June 13 at 15 cm. Germination in the field was greatest at the surface but was observed at all soil levels by March 21. Seedling survival was 68% at the surface and 0% at 5 and 15 cm on June 13. Maximum and minimum soil temperatures were recorded at each soil level during the experiment and were correlated with the results. Greater germination and survival at the surface supports the evidence for ragweed's dependence on soil disturbance for germination, and the induction of secondary dormancy explains why ragweed does not constitute a dominant part of the vegetation when disturbance occurs after the soil warms to a critical point in the summer.     

TWO TYPES OF MORPHOPHYSIOLOGICAL DORMANCY IN SEEDS OF TWO GENERA (OSMORHIZA AND ERYTHRONIUM) WITH AN ARCTO-TERTIARY DISTRIBUTION PATTERN

Temperature requirements for embryo growth and germination were determined for seeds of Osmorhiza occidentalis, O. chilensis, and Erythronium grandiflorum collected in western North America (Utah). Initially, embryos were 1.2, 0.6, and 0.8 mm in length, respectively, and they grew to 9.4, 9.2, and 4.1 mm, respectively, before germination occurred. Embryo growth and germination occurred during cold stratification (1, 5, 5/1 C), without a warm stratification pretreatment. However, warm stratification pretreatments at 30/15 C increased rates of embryo growth in O. occidentalis and E. grandiflorum seeds moved to low temperatures and germination rates in all three species. Optimum germination temperatures were 1, 5, or 5/1 C; gibberellic acid did not substitute for cold stratification. Thus, seeds of the three species have deep complex morphophysiological dormancy (MPD). In comparison, two species each of Osmorhiza and Erythronium from eastern North America have nondeep complex MPD and require warm followed by cold stratification for germination. Thus, disjunct species in genera with an Arcto-Tertiary distribution pattern can have different types of MPD. It is suggested that deep complex may have been derived from nondeep complex MPD.     

休眠与萌发过程中苹果种子的呼吸代谢

“秦冠”苹果种子的总呼吸强度和EMP途径的呼吸强度在2℃条件下层积之后逐渐增加,解除休眠临界期大体在层积后第30天发生,此后增长速度较快。HMP途径和TCAC在临界期之前变化极慢,而后急剧增加。种子萌发后子叶和胚轴的总呼吸强度、EMP和TCAC初期呈急剧上升趋势,大约当胚轴长度达2cm时迅速下降,HMP在萌发过程中始终呈上升趋势。细胞透性层积之后逐渐降低,解除休眠至萌发阶段呈上升趋势。用不同浓度呼吸抑制剂处理解除休眠种子的试验结果表明,除1mM碘乙酸能明显刺激萌发和生长外,NaCN、SHAM和丙酮酸都表现为抑制作用。     

REPRODUCTIVE STRATEGY OF CLEISTES DIVARICATA (ORCHID ACEAE)

In Cleistes divaricata, a hinged anther dispenses a sequence of loosely aggregated pollen tetrad masses onto the dorsal thorax of Bombus and Megachile workers. This mechanism allows more than one bee to receive pollen from a single flower. To determine the effectiveness of this strategy, plants in bud were caged and hand pollinated using pollen from sequential releases. Capsules produced from a flower's first three pollen dumps were significantly larger and heavier and contained more seeds than those produced by later pollen deposits with fewer tetrads. Decreasing pollen dosage did not affect fruit set, capsule development, individual seed weight, or percentage of healthy looking embryos per fruit. Fruit set for artificial pollinations was 93% for pollen dumps 1–3 and 97% for dumps 4–18. As set of naturally pollinated marked plants was only 38%, low frequency of pollinator visits apparently limited seed production. Efficacy of infrequent visits is maximized, however, because a flower's first pollen releases contain the most pollen, but later low-dosage dumps can produce some seeds. An unexpected cost was a higher investment of pericarp per seed in low-dosage capsules (130 ng pericarp seed^-1 fresh weight) than in high-dosage pollinations (only 27 ng pericarp seed^–1). Flower fading in plants receiving low pollen dosage was as slow as that in caged, unpollinated controls, thus increasing opportunity for additional pollination.     

DORMANCY AND GERMINATION IN SEEDS OF COMMON RAGWEED WITH REFERENCE TO BEAL'S BURIED SEED EXPERIMENT

Common ragweed (Ambrosia artemisiifolia L.) was one of 19 herbaceous weedy species used by Beal in his buried viable seed experiment started in 1879. No seeds germinated during the first 35 years of the experiment when germination tests were performed in late spring, summer or early autumn. Germination did occur in seeds buried for 40 years when seeds were exhumed and tested for germination in early spring. Data obtained in more recent research provide the probable explanation for these results. Seeds of common ragweed that do not germinate in spring enter secondary dormancy by mid to late spring and will not germinate until dormancy is broken the following late autumn and winter. Thus, during the first 35 years of the experiment seeds were dormant when tested for germination, whereas seeds buried for 40 years were nondormant. Seeds buried 50 years or longer did not germinate when tested in spring, probably because they had lost viability and/or seeds germinated during burial and seedlings died.     

桦叶荚蒾种子的休眠和催芽研究

桦叶英莲是一种经济和观赏植物。它的种子的下胚轴和上胚轴都有休眠。在自然条件下,下胚轴的休眠期长达295—420天,上胚轴的休眠期长达50—120天。下胚轴的休眠可用暖层积打破,上胚轴的休眠可用冷层积打破。种子经硫脲处理和在人工控制的条件下,下胚轴的休眠可比自然条件下的缩短近一半。GA和暖处理对解除上胚轴的休眠没有影响。子叶的去留和暗处理对上胚轴萌发的作用不大。     

PHYSIOLOGICAL BASIS OF ACHENE DORMANCY IN POLYGONUM CONVOLVULUS (POLYGONACEAE)

Germination of dormant achenes of wild buckwheat (Polygonum convolvulus L.) was promoted at 25 C if they were stratified at low temperatures. Preincubation at either 2 C or 10 C promoted subsequent germination at 25 C equally, although the period of time to reach maximum germination was shorter for the 2 C treatment. Moreover, a preincubation treatment of a daily alternating cycle 2 C for 20 hr and 10 C for 4 hr promoted germination at 25 C more than either temperature alone. Removing portions of the hard pericarp and testa did not promote germination of dormant achenes at 25 C except when the portion of those structures covering the tip of the radicle was removed. This suggests that the structures covering the embryo do not prevent germination by restricting the movement of water or gases but rather restrict growth mechanically. Complete removal of the pericarp promoted germination, but much higher germination was obtained when the testa was also removed, indicating that the pericarp may not be the main factor in dormancy. Thus the role of low temperature in the loss of dormancy in wild buckwheat achenes may be to promote the production of hydrolytic enzymes that lower the mechanical resistance of pericarp and testa and/or increase the embryo growth potential beyond some threshold level and thereby enable the radicle to overcome the resistance to growth imposed by the structures covering the embryo.     

豚草和三裂叶豚草种子休眠规律研究

豚草和三裂叶豚草是菊科豚草属一年生草本植物,其种子休眠程度随生育地的纬度不同而有变化,纬度越高,种子成熟后进入休眠状态的比例越大,解除休眠所需的低温层积时间也越长。在高纬度的牡丹江市,成熟的豚草和三裂叶豚草种子全部进入休眠状态,低温层积１２周时萌发率达９５％以上,而在低纬度的南昌市,有１０％左右的豚草和三裂叶豚草种子没有进入休眠状态,低温层积８周时,萌发率即可达９５％以上。进入休眠状态的豚草和三裂叶豚草种子,不经过低温层积处理,在１５℃的室温下保存半年以上,也有一定比例的种子可以解除休眠。豚草和三裂叶豚草种子休眠机制可能是由抑制物质和促进物质复合体所控制,休眠种子含有高水平的抑制剂和低水平的促进剂,非休眠种子这种平衡转向有利于促进剂,不同纬度地区的温度差异和低温层积以及长期室温贮藏的呼吸代谢过程,可能对这种平衡产生影响,改变种子的休眠状态     

乙烯与水浮莲(Pistia stratiotes)种子需光性休眠的关系

水浮莲种子是一种奇特的需光种子。在黑暗中,GA_2或BA均不能代替光照诱导萌发,可是0.1μl/l乙烯却能引起部分种子萌发,在1000μ1/1乙烯的作用下,发芽率可达80％,接近全光照处理的萌发水平(91％发芽率)。ACC也能诱导水浮莲种子的萌发,0.1 mM浓度可获30％发芽率。在较短光照下,ACC对种子萌发有增效作用。在光照前应用ACC,其诱导效应大于两者同时施用。在照光萌发中,种子的内源ACC含量及乙烯释放量均显著增加。CoCl_2和AOA均能抑制光的诱导萌发。推论光打破休眠诱导萌发的作用是与乙烯的生成密切相关。     

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

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