Gehan Jayasuriya K M G, Baskin Jerry M, Geneve Robert L, Baskin Carol C
Department of Biology, University of Kentucky, Lexington, KY 40506, USA.
Ann Bot. 2007 Sep;100(3):459-70. doi: 10.1093/aob/mcm137. Epub 2007 Jul 24.
Disruption of one or both of the bulges (water gap) in the seed coat adjacent to the micropyle is responsible for breaking physical dormancy (PY) in seeds of Ipomoea lacunosa and other taxa of Convolvulaceae. Hitherto, neither ontogeny of these bulges nor onset of PY together with anatomical development and maturation drying of the seed had been studied in this family. The aims of this study were to monitor physiological and anatomical changes that occur during seed development in I. lacunosa, with particular reference to ontogeny of the water gap.
Developmental anatomy (ontogeny) of seed coat and dry mass, length, moisture content, germinability and onset of seed coat impermeability to water were monitored from pollination to seed maturity. Blocking/drying and dye-tracking experiments were done to identify site of moisture loss during the final stages of seed drying.
Physiological maturity of seeds occurred 22 d after pollination (DAP), and 100 % of seeds germinated 24 DAP. Impermeability of the seed coat developed 27-30 DAP, when seed moisture content was 13 %. The hilar fissure was identified as the site of moisture loss during the final stages of seed drying. The entire seed coat developed from the two outermost layers of the integument. A transition zone, i.e. a weak margin where seed coat ruptures during dormancy break, formed between the bulge and hilar ring and seed coat away from the bulge. Sclereid cells in the transition zone were square, whereas they were elongated under the bulge.
Although the bulge and other areas of the seed coat have the same origin, these two cell layers underwent a different series of periclinal and anticlinal divisions during bulge development (beginning a few hours after pollination) than they did during development of the seed coat away from the bulge. Further, the boundary between the square sclereids in the transition zone and the elongated ones of the bulge delineate the edge of the water gap.
紧挨珠孔的种皮凸起(水隙)一处或两处遭到破坏会打破缺萼飞蛾藤及旋花科其他类群种子的物理休眠(PY)。迄今为止,该科尚未对这些凸起的个体发育以及休眠与种子的解剖学发育和成熟干燥过程的起始进行研究。本研究的目的是监测缺萼飞蛾藤种子发育过程中发生的生理和解剖变化,尤其关注水隙的个体发育。
从授粉到种子成熟,监测种皮的发育解剖(个体发育)、干质量、长度、含水量、发芽能力以及种皮不透水性的起始。进行了阻断/干燥和染料追踪实验,以确定种子干燥最后阶段水分流失的部位。
种子在授粉后22天(DAP)达到生理成熟,24 DAP时100%的种子发芽。种皮不透水性在27 - 30 DAP形成,此时种子含水量为13%。脐裂缝被确定为种子干燥最后阶段水分流失的部位。整个种皮由珠被的最外层两层发育而来。在凸起和脐环与远离凸起的种皮之间形成了一个过渡区,即休眠破除期间种皮破裂的薄弱边缘。过渡区的石细胞呈方形,而在凸起下方则呈细长形。
尽管种皮的凸起和其他区域起源相同,但这两层细胞在凸起发育期间(授粉后数小时开始)经历的平周分裂和垂周分裂系列与远离凸起的种皮发育期间不同。此外,过渡区方形石细胞与凸起处细长石细胞之间的边界划定了水隙的边缘。