...
首页> 外文期刊>Invasive Plant Science and Management >Laboratory methods for breaking dormancy in garlic mustard (Alliaria petiolata) seeds.
【24h】

Laboratory methods for breaking dormancy in garlic mustard (Alliaria petiolata) seeds.

机译:打破大蒜芥末( Alliaria petiolata )种子休眠的实验室方法。

获取原文
获取原文并翻译 | 示例
           

摘要

Garlic mustard seeds are dormant at maturity, and 90 to 105 d of cold-moist stratification at 4 C have been used to induce germination. We studied methods for breaking dormancy and inducing germination without cold stratification, for use in laboratory and greenhouse experiments with garlic mustard. Seeds were collected from large infestations, stored at room temperature, and subjected to chemical and mechanical scarification treatments. For chemical scarification, seeds were immersed in 3% (v/v) H2O2 for 12, 24, or 48 h with constant stirring, or immersed in concentrated (95 to 97%) H2SO4 for 1 or 5 min with stirring. For mechanical scarification, seeds were placed in a sandpaper-lined tumbler for 1 or 3 s. Scarified seeds, along with non-scarified seeds, were placed in petri dishes on germination blotters saturated with gibberellic acid (GA3, 10-3 M) or deionized water, and incubated for 35 d at either 20/10 C or 15/6 C (12 hr/12 hr). None of the non-scarified seeds germinated, regardless of germination solution or temperature. Seeds germinated only following scarification, and only when imbibed in GA3 solutions. Seeds immersed in H2SO4 for 5 min or mechanically scarified for 3 s had the highest level of germination in GA3. Cumulative percent germination after 35 d was greater for seeds stored 30 mo (44 to 83%), than for seeds stored 6 (2 to 60%) or 18 mo (35 to 79%), regardless of scarification treatment. The germination results, along with scanning electron micrographs of seed coats, suggest that the intact garlic mustard seed coat is permeable to water but not GA3; therefore, both scarification and GA3 are needed to break dormancy and induce germination without cold stratification.
机译:大蒜芥末种子在成熟时处于休眠状态,并且已在4 C下使用90至105 d的冷湿分层法来诱导发芽。我们研究了在不进行冷分层的情况下打破休眠并诱导发芽的方法,用于蒜芥的实验室和温室实验。从大批侵染中收集种子,在室温下保存,并进行化学和机械划痕处理。对于化学划痕,将种子在不断搅拌下浸入3%(v / v)H 2 O 2 达12、24或48 h,或浸入浓缩的( 95%至97%)的H 2 SO 4 搅拌1至5分钟。为了机械除草,将种子放在衬有砂纸的滚筒中1或3 s。将经过脱毛的种子和未脱钙的种子一起放在培养皿中的培养皿中,培养皿上装有赤霉素(GA 3 ,10 -3 M)或去离子水,在20/10 C或15/6 C(12 hr / 12 hr)下孵育35 d。不论发芽溶液或温度如何,所有非钙化种子均不会发芽。种子仅在划痕后萌发,并且仅在GA 3 溶液中萌发。 GA 3 中浸入H 2 SO 4 5分钟或机械刮擦3 s的种子​​发芽水平最高。无论是否进行松散处理,储存30 mo的种子(44%至83%)在35 d后的累积发芽百分比大于储存6 mo(2%至60%)或18 mo(35%至79%)的种子。种子发芽的结果以及种皮的扫描电子显微镜照片表明,完整的大蒜芥末种皮可透水,但GA 3 不透水;因此,为了消除休眠并诱导发芽而无需冷分层,既需要划痕也需要GA 3

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号