迷迭香工厂化育苗技术

用迷迭香小苗枝条为外植体进行组织培养，用组培苗嫩梢作为插穗进行扦插育苗试验。结果表明：芽增殖以MS＋6BA0.5mg/L NAA0.01mg/L 蔗糖30g/L培养基的增殖率达1.4倍；不定根诱导以1／3MS＋IBA0.5mg/L 蔗糖20g/L的培养基效果好，生根率达100％；以组培苗嫩梢扦插，生根率达98％以上。利用芽增殖培养→生根炼苗培养→移栽上盆→扦插→出圃这一流程生产苗木，成本低、苗木质量优、繁殖速度快，可在生产上推广应用。     

米良一号猕猴桃的组织培养研究

米良一号猕猴桃外植体在不同激素的MS培养基上培养．结果表明：①诱导培养基以MS 1．0mg／L ZT为好，材料不经转移可直接分化出丛生芽，ZT浓度在1．5mg／L以上时，对愈伤组织形成有抑制作用，且在1．5mg／L ZT的同时．加0．5mg／L 6-AB，这2种细胞分裂素超量后的抑制作用是累加的，致使抑制作用加剧无芽茎段褐化死亡；②出芽周期长短与茎段年龄和有芽无芽有关，成熟茎段出芽早，幼嫩茎段出芽迟，有芽茎段出芽早，无芽茎段出芽迟，幼嫩的无芽茎段出芽虽晚30d左右．但由愈伤组织形成的丛芽多得多；③米良一号生根能力不强，出芽后不经生根诱导不能生根，1／2MS 1．0mg／L IBA 30g／L蔗糖，有较好的诱导生根作用；④叶片培养再生率正交实验结果表明生长素优先因子顺序为ZT、6-BA、NAA、TDZ，叶的最佳诱导分化培养基为MS 10mg／LBA 0．2mg／L NAA 1．0mg／L TDZ。     

核桃试管苗生根培养的研究

以新疆绵核桃为试材,对继代培养无根试管苗的生根进行了研究.结果表明：生根诱导方法、外源IBA水平及IBA处理时间、光周期以及试管苗发育状态等均对不定根发生具有明显影响.选取生长旺盛、节间较长,叶片嫩绿的幼态苗,采用间接诱导生根法,即用50～80 mg/L IBA浸渍处理试管苗基部60～90 min,然后转至不含生长调节物质的1/2 DKW培养基,先黑暗诱导14 d,再在16 h/d光照下培养,可诱导试管苗生根率达60%以上.     

红蝉花的组织培养及快速繁殖技术

以红蝉花(Mandevilla sanderi)带腋芽的成熟茎段、幼嫩茎段和茎尖作为外植体进行试管培养的结果表明：茎尖是初代培养最适合的外植体，MS BA2．0～4．0mg／L NAA0．1mg／L有利于外植体腋芽的萌生；最有效的芽增殖培养基为MS BA4．0mg／L NAA0．01mg／L，增殖系数达到4．3；最有效的生根培养基为MS NAA2．0mg／L C0．2％，生根率可达76．7％。     

几种造纸用丛生竹秆节育苗试验

在福建省邵武市对椽竹、孝顺竹、坭竹等几种造纸用丛生竹进行秆节育苗试验表明，用平埋方法育苗显著优于斜埋和直插，竹蔸平埋效果更佳；不同竹种秆节育苗成活率存在明显差异；不同年龄的秆节育苗成活率在不同竹种间表现不同；不同育苗时间（３月或５月）的成活率差异不显著。竹秆不同粗细、不同部位、单节段或双节段育苗对比试验，结果以细秆（胸径２．５ｃｍ）、上部节段、双节段育苗成活率较粗秆（胸径４．６ｃｍ）、下部节段、单节段的为高。椽竹秆节径用不同激素处理后，处理间成苗率差异显著，以２，４－Ｄ２０ｍｇ／ｋｇ处理５ｈ和硼酸２０ｍｇ／ｋｇ处理２４ｈ的效果最佳。几种造纸用丛生竹秆节育苗试验＊张文燕周道三马乃训叶长青曹德友张华明     

Tree growth and stand development of four Populus clones in large monoclonal plots

Four clones of Populus were planted in replicated monoclonal plots near Olympia, WA, to evaluate their suitability for use in short-rotation culture. All clones were easily established and had minimal problems from damaging agents during the first five years. Observed differences among clones in pattern and amount of growth appeared to be associated with differences in number and density of buds, sylleptic branching, and phenology. In addition, differences in drought tolerance and stockability may also have influenced clonal differences in annual growth and stand productivity. Individual tree growth was limited by the dense 1.0-m spacing, but the best-growing clones averaged 13 to 16 m tall, 7 to 9 cm in breast-high diameter (1.3 m), and produced stand basal areas exceeding 38 m²ha^-1at 8 years. Mortality was negligible for 7 years, after which various combined effects of competition, stem borer damage (Cryptorhyncus lapathi), and a severe windstorm caused mortality ranging from 18 to 36% in the three fastest growing clones.     

丽格海棠的离体快繁研究

组培快繁技术研究结果表明:适宜丽格海棠叶片诱导芽分化的培养基为MS 6 BA0 50mg/L NAA1 00mg/L;适宜丛生芽继代增殖的培养基为MS 6 BA0 25mg/L NAA1 00mg/L;适宜丽格海棠试管苗生根的培养基为1/2MS,其生根率为100%。     

信阳板栗低产林综合改造技术的研究

信阳市板栗生产中普遍存在产量低,品质差问题,本文通过对板栗低产原因的分析,为开发板栗资源,提出了优质高产栽培的重要途径和措施。     

Somatic embryo culture for propagation,artificial seed production,and conservation of sawara cypress (<Emphasis Type="Italic">Chamaecyparis pisifera</Emphasis> Sieb. et Zucc.)

 Somatic embryogenesis in Chamaecyparis pisifera Sieb. et Zucc. was initiated from immature seeds collected from the end of June to early July. Mass propagation through adventitious shoot bud production from somatic embryo culture on Woody Plant (WP) medium and artificial seed production using sodium alginate was achieved. A high bud forming index value (25.8) was obtained on medium supplemented with 1 μM 6-benzylaminopurine. The conversion rates from artificial seeds under aseptic and nonaseptic conditions were 60%–100% and 10%–12%, respectively. For germplasm conservation, somatic embryos and embryogenic cells were successfully stored at 4°C (medium-term storage) and in liquid nitrogen for long-term storage. Received: December 21, 2001 / Accepted: August 1, 2002 Acknowledgments This work was supported in part by the Japan Science and Technology Corporation and in part by a Grant for Research for the Future Program from the Japan Society for the Promotion of Science. Correspondence to:E. Maruyama     

Liquid culture and transformation of hinoki cypress (Chamaecyparis obtusa Sieb. et Zucc.)

Hinoki cypress (Chamaecyparis obtusa) is one of the most important timber resource forest trees in Japan. Because seed production from a seed orchard of hinoki cypress is not constant every year, micropropagation from a limited amount of material is useful. Up to now, the conventional tissue culture method using solid medium has been used. Here a new method using liquid culture in tubes rotated vertically is described. Shoot primordium of hinoki cypress was inoculated in Campbell and Durzan’s (CD) liquid medium containing different cytokinins (6-benzylaminopurine (BAP), Zeatin, thidiazurone (TDZ)), and the container tubes were rotated vertically around the axis at 2 times / min. Culture room temperature was 25°C and light condition was 16 h photoperiod per day of fluorescent lamps. Zeatin at 1μM concentration was the best for maintaining the shoot primordium production and TDZ induced callus on the surface of the shoot primordia. After shoot primordium multiplication in the liquid culture, they were transplanted to agar medium for shoot elongation. A high concentration of agar (up to 16 g/L) or AVF (anti vitrification factor from Dr. Nairn, 1995) was effective to prevent vitrification of the shoots. Transformation of shoot primordium was done using particle bombardment with vectors containingβ-glucuronidase (GUS) gene or herbicide resistance gene (bar). Positive result for transient transformation was observed with the histo-chemical study for transformation with GUS. Integration of a useful herbicidebar gene into the shoot primordium culture system was also tried and stably transformed plants were obtained. This is the first report of stable transformation of Japanese conifer using practically useful gene. The generous supply of AVF-B from Dr. B.J. Nairn, Tasman Forestry, NZ is also appreciated.