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舞钢玉兰芽种类与成枝成花规律的研究 被引量:24
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作者 赵天榜 高炳振 +2 位作者 傅大立 周惠茹 陈志秀 《武汉植物学研究》 CSCD 2003年第1期81-90,共10页
报道了舞钢玉兰芽的种类、分枝习性与成枝生长规律 ,拟花蕾、着生位置、解剖结构及其分化发育成花规律。从中发现 :(1)当年生枝上有休眠芽、叶芽 (侧叶芽和顶叶芽 )、拟花蕾 3种 ;(2 )拟花蕾有缩台枝、芽鳞状托叶、雏枝、雏芽及雏蕾组... 报道了舞钢玉兰芽的种类、分枝习性与成枝生长规律 ,拟花蕾、着生位置、解剖结构及其分化发育成花规律。从中发现 :(1)当年生枝上有休眠芽、叶芽 (侧叶芽和顶叶芽 )、拟花蕾 3种 ;(2 )拟花蕾有缩台枝、芽鳞状托叶、雏枝、雏芽及雏蕾组成 ,因其外形似“花蕾”,称为“拟花蕾” ;(3)缩台枝是枝与花着生的中间过渡枝变阶段 ,是由母枝顶端节间缩短、增粗的枝段和当年由雏枝生长的 1次极短新枝所组成 ;(4 ) 4~ 5月及 7~ 8月前后两批形成的拟花蕾 ,均经过未分化发育期、花被分化发育期、雄蕊群分化发育期及离心皮雌蕊群分化发育期 ,各期均依次递后交错进行 ,但不逆转 ,也不能截然分开 ,直到翌春花分化发育全部结束 ,开花后才能结实 ;(5 )芽鳞状托叶是托叶的变态 ,最外层薄革质 ,外面密被短柔毛 ,始落期 6月中下旬 ,其余纸质——膜质 ,外面密被或疏被长柔毛 ,翌春开花时脱落完毕 ;(6 )雏蕾有雏梗、雏花及包被雏花的佛焰苞状托叶组成 ;(7)分枝习性与成枝生长规律为预生分枝及预生一同生分枝呈单阶无歧、单阶 1歧生长规律 ,稀有单阶 2歧生长规律。 展开更多
关键词 舞钢玉兰 芽种类 拟花蕾 缩台枝 生长习性 拟花蕾分化 玉兰属
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木兰属等3属植物的芽种类、结构与成枝规律研究 被引量:3
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作者 陈建业 鲁国荣 +2 位作者 宁玉霞 赵天榜 陈志秀 《中国农学通报》 CSCD 2012年第34期46-52,共7页
为进一步了解木兰亚枓植物有预生分枝、同生分枝的科学性、真实性,及其在该亚科分类系统中的应用前景,选取木兰属、玉兰属和含笑属等3属植物的代表种——荷花木兰、玉兰、耐冬含笑,对其芽种类、结构解剖、分枝习性等进行研究。结果表明:... 为进一步了解木兰亚枓植物有预生分枝、同生分枝的科学性、真实性,及其在该亚科分类系统中的应用前景,选取木兰属、玉兰属和含笑属等3属植物的代表种——荷花木兰、玉兰、耐冬含笑,对其芽种类、结构解剖、分枝习性等进行研究。结果表明:(1)荷花木兰芽有4种:盲芽、休眠芽、叶芽、混合芽;玉兰芽有3种:休眠芽、叶芽、玉蕾;耐冬含笑芽有4种:休眠芽、叶芽、花蕾、混合芽。同时,首次发现含笑属有混合芽及单歧聚伞花序。3属混合芽与玉蕾区别显著,具有系统学意义。(2)Figlar提出的预生分枝和同生分枝的基础不同,无可比性,无系统学意义。荷花木兰等植物均具有预生分枝及预生-同生分枝,绝无同生分枝的现象。其成枝规律随树种、立地条件、栽培技术、树龄不同,且区别明显。Figlar以分枝习性不同,将合笑属并入木兰属是不妥的。 展开更多
关键词 荷花木兰 玉兰 耐冬含笑 芽种类 结构解剖 成枝生长规律
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Response to temperature stress of reactive oxygen species scavenging enzymes in the cross-tolerance of barley seed germination 被引量:8
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作者 Yu-qin MEI Song-quan SONG 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE CAS CSCD 2010年第12期965-972,共8页
A number of studies have shown the existence of cross-tolerance in plants, but the physiological mechanism is poorly understood. In this study, we used the germination of barley seeds as a system to investigate the cr... A number of studies have shown the existence of cross-tolerance in plants, but the physiological mechanism is poorly understood. In this study, we used the germination of barley seeds as a system to investigate the cross-tolerance of low-temperature pretreatment to high-temperature stress and the possible involvement of reactive oxygen species (ROS) scavenging enzymes in the cross-tolerance. After pretreatment at 0 ℃ for different periods of time, barley seeds were germinated at 35 ℃, and the content of malondialdehyde (MDA) and the activities of ROS scavenging enzymes were measured by a spectrophotometer analysis. The results showed that barley seed germinated very poorly at 35 ℃, and this inhibitive effect could be overcome by pretreatment at 0 ℃. The MDA content varied, depending on the temperature at which seeds germinated, while barley seeds pretreated at 0 ℃ did not change the MDA content. Compared with seeds germinated directly at 35 ℃, the seeds pretreated first at 0 ℃ and then germinated at 35 ℃ had markedly increased activities of superoxide dismutase (SOD), ascorbate peroxidase (APX), catalase (CAT), and glutathione reductase (GR). The SOD and APX activities of seeds germinated at 35 ℃ after 0 ℃-pretreatment were even substantially higher than those at 25 ℃, and GR activity was similar to that at 25 ℃, at which the highest germination performance of barley seeds was achieved. These results indicate that low-temperature pretreatment can markedly increase the tolerance of barley seed to high temperature during germination, this being related to the increase in ROS scavenging enzyme activity. This may provide a new method for increasing seed germination under stress environments, and may be an excellent model system for the study of cross-tolerance. 展开更多
关键词 Barley seed CROSS-TOLERANCE Germination/growth Reactive oxygen species (ROS) scavenging enzyme Pretreatment at low temperature Temperature stress
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