首页> 外文学位 >CLONAL PROPAGATION OF ENDANGERED NATIVE PLANTS RHODODENDRON CHAPMANII GRAY, TAXUS FLORIDANA NUTT., AND TORREYA TAXIFOLIA ARN. (MICROPROPAGATION, IN VITRO/TISSUE CULTURE, PLANT PROPAGATION, WOODY ORNAMENTALS).
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CLONAL PROPAGATION OF ENDANGERED NATIVE PLANTS RHODODENDRON CHAPMANII GRAY, TAXUS FLORIDANA NUTT., AND TORREYA TAXIFOLIA ARN. (MICROPROPAGATION, IN VITRO/TISSUE CULTURE, PLANT PROPAGATION, WOODY ORNAMENTALS).

机译:濒危原生植物杜鹃花CHAPMANII灰色,TAXUS FLORIDANA NUTT。和TORREYA TAXIFOLIA ARN的克隆繁殖。 (微繁殖,体外/组织培养,植物繁殖,木质装饰物)。

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摘要

Clonal propagation utilizing conventional and micropropagation techniques was investigated for three endemic and endangered Florida plant species, Rhododendron chapmanii Gray, Taxus floridana Nutt. and Torreya taxifolia Arn. This is critical for their preservation since these species exist in limited numbers but have high ornamental value which has threatened their survival due to illegal collection.;Torreya and Taxus cuttings could be easily propagated when treated with 2,000-4,000 mg/l IBA. However, cuttings taken from lateral branches demonstrated strict plagiotropic growth. Best rooting and growth of Torreya cuttings (20%) occurred following treatment with 4000 mg/l IBA. Taxus cuttings rooted best (67%) following treatment with 2000 mg/l IBA.;Shoot-tip cultures (3-5 cm long) of Taxus and Torreya developed only 2-3 lateral shoots, apparently from preformed buds. Cultured "embryonic shoots" from expanding vegetative buds failed to produce multiple shoots. Excised embryos did not germinate following liquid culture to leach inhibitors. Micro- and megasporangia did not grow or differentiate in culture.;The most promising technique for Torreya involved application of cytokinins (4 weekly sprays with 100-200 mg/l BA or 2-i-P) to seedlings before culture. Newly stimulated axillary shoots developed additional shoots and multiple "bud-masses" when cultured on WPM with BA (1 mg/l) and NAA (0.01 mg/l). These were slow to develop but could be subcultured with additional growth of multiple shoots. No rooted plantlets were obtained.;Micropropagation of R. chapmanii was investigated using shoot-tip cultures. An average of 7.6 fold increase in lateral shoots was achieved for three additional Stage II multiplication cycles on low salts Woody Plant Medium (WPM) with 2-i-P (10 mg/l) and adenine sulfate (80 mg/l). Microcuttings rooted in 4-6 weeks when direct-stuck into autoclaved 1:1:1 (v:v:v) Canadian peat:vermiculite:perlite medium in covered flats. A 5 second quick-dip in 1000 mg/l IBA (20% EtOH + 80% H(,2)O) increased survival and rooting of microcuttings. Inoculation of plantlets with the mycorrhizal fungus, Pezizella ericae increased survival and growth when plantlets were established in a less than optimal soil-less medium (1:1 v:v Fired montmorillonite clay:Canadian peat) but not in MetroMix-500.
机译:利用常规和微繁殖技术,对三种特有和濒危佛罗里达植物,杜鹃花查普曼尼·格雷,南方红豆杉的克隆繁殖进行了研究。和托雷娅的士兰阿恩。这对于它们的保护至关重要,因为这些物种数量有限,但具有很高的观赏价值,由于非法采摘而威胁到它们的生存。用2,000-4,000 mg / l IBA处理的Torreya和Taxus插条很容易繁殖。然而,取自侧枝的插条显示出严格的斜生性生长。用4000 mg / l IBA处理后,香Torre插条生根和生长最佳(20%)。用2000 mg / l IBA处理后,红豆杉插条生根最好(67%)。红豆杉和Torreya的尖顶培养物(长3-5 cm)仅形成2-3个侧生芽,显然是来自预先形成的芽。来自不断增长的营养芽的培养“胚芽”未能产生多芽。液体培养后浸出的抑制剂不会使胚萌发。微孢子囊和大孢子囊菌没有在培养中生长或分化。;托雷亚最有前途的技术涉及在培养前向幼苗施用细胞分裂素(4次每周喷洒100-200 mg / l BA或2-i-P)。当在WPM上用BA(1 mg / l)和NAA(0.01 mg / l)培养时,新刺激的腋生芽形成更多的芽和多个“芽团”。这些植物发育缓慢,但可以通过多芽的额外生长进行继代培养。没有生根的小植株。;使用芽尖培养物研究了查普曼红杆菌的微繁殖。在具有2-i-P(10 mg / l)和硫酸腺嘌呤(80 mg / l)的低盐木本植物培养基(WPM)上进行的另外三个II期繁殖循环,侧枝平均增加了7.6倍。当直接嵌入高压灭菌的1:1:1:1(v:v:v)加拿大泥炭:ver石:珍珠岩培养基中的微型地板中时,可在4-6周内扎根。在1000 mg / l IBA(20%EtOH + 80%H(,2)O)中浸泡5秒可增加微切屑的存活率和生根。当在不太理想的无土培养基(1:1 v:v焙烧蒙脱土:加拿大泥炭)中建立小植株时,用菌根真菌Pezizella ericae接种小植株可提高存活和生长,但在MetroMix-500中则不能。

著录项

  • 作者

    BARNES, LEE ROY, JR.;

  • 作者单位

    University of Florida.;

  • 授予单位 University of Florida.;
  • 学科 Agriculture Plant Culture.
  • 学位 Ph.D.
  • 年度 1985
  • 页码 85 p.
  • 总页数 85
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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