毛乌素沙地东南缘植被恢复中优势灌木的保育作用分析

以毛乌素沙地东南缘优势灌木作为保育植物,选择油松(Pinus tabulaeformis)和樟子松(Pinus sylvestris)幼苗作为目标物种,将其分别种植在开阔地和优势灌木冠层下,连续3 a统计松树幼苗的存活率和主枝生长长度,从而确定毛乌素沙地优势灌木对松树幼苗的定居是否存在保育作用。同时,测量开阔地和灌木冠层下的环境指标,揭示优势灌木保育作用产生的机理。结果表明:1优势灌木冠层下松树幼苗的总存活率显著高于开阔地(P0.05),说明优势灌木可增加松树幼苗的存活率。2在持续3 a的恢复实验期间,优势灌木对松树幼苗定居的保育作用不随时间的变化而发生改变。3优势灌木冠层下松树幼苗的主枝生长良好,并未受到抑制。4优势灌木通过改善微环境,从而对其冠层下松树幼苗的定居产生保育作用,其中改善最为明显的是光照强度和土壤湿度,其次是土壤的有机质和全氮含量。总的来说,优势灌木对松树幼苗的定居存在保育作用,保育植物技术可作为一种有效的恢复措施,应用在毛乌素沙地东南缘的植被恢复中,从而为该区植被的恢复与生态保护提供基础数据。     

利用自制骨炭除氟剂处理农村高氟地下水研究

在不同实验条件下将家畜骨制成骨炭除氟剂,通过除氟效果的比较筛选出最佳除氟剂制备方法。利用所制得的骨炭进行除氟静态吸附实验,研究了骨炭对氟的吸附效果以及温度、pH和地下水中常见阴阳离子等不同影响因素对骨炭除氟效果的影响。实验结果表明温度对骨炭除氟效果影响不大;低pH条件有利于骨炭对氟的去除;地下水常见阴阳离子中,Ca2＋和Mg2＋对骨炭除氟有一定的促进作用,而阴离子则起到不同程度的抑制作用。除氟后的骨炭可以利用NaOH浸泡方法进行再生,经三次再生后其吸附容量仍可达原来的94.3%,说明骨炭除氟剂具有良好的再生能力且可反复用于水中除氟。     

油松林内横山叠梗天然更新试验

为防止雨水将油松落果和种子冲击至山下腹或沟谷,影响自然撒种更新数量,进行了横山叠梗的留存种子方法试验,结果表明横山叠梗可大量提高油松的更新数量,试验区平均更新量为523.6万株hm^-2,是对照区更新量的5.29倍.油松林内横山叠梗天然更新效果显著.     

湘南典型残次阔叶林人工促进更新技术研究

于2003年在湖南省汝城县益将国有林场天然残次阔叶林内设置试验样地和对照样地各3个,采用林地清理、补植、补播等手段促进天然更新,并分别于2006年和2011年进行2次人工促进干预;同时,在6个样地内各设置3个样方,共计18个样方,分别于2003、2008、2013年冬,对幼树、幼苗、萌条的数量及地径进行统计,并对样方内胸径≥5 cm的立木进行每木调查。结果表明:种子补播保存率43%,幼苗补植保存率20%,平均保存率32%。树高≤30 cm且地径0.5 cm、31 cm≤树高≤50 cm且0.5 cm地径0.7 cm幼树的数量下降率分别是对照样地的17.5%、21.59%,树高≥51 cm且地径0.7 cm幼树的数量下降率是对照样地的121.66%。2008年单位面积蓄积量是对照样地的2.28倍,2013年达到3.80倍;经过10年更新,单位面积蓄积量是试验前的11.57倍,对照样地单位面积蓄积量仅是试验前的2.55倍;单位面积蓄积量是对照样地的4.54倍。人工促进天然更新所需的人工成本为1 860元/hm2,仅为同期人工营造杉木幼林所需人工成本5 310元/hm2的35%。     

冰草属植物组织培养再生体系的建立

以适宜西北地区种植的优质牧草冰草属(AgropyronGaertn)中的三个不同种———蒙古冰草新品系(A.mongolicumKeng)、航道冰草(A.cristatumcv.Fairway)、诺丹冰草(A.desertorumcv.Nordan)和一个种间杂种冰草———蒙农杂种冰草(A.cristatum×A.desertorumcv.Mengnong)为材料,分别以幼穗为外植体建立了冰草组织培养再生体系。诱导愈伤组织的培养基为改良MS+2,4 D2.0mg/L,分化培养基为MS(无附加成分),在1/2MS培养基上生根后得到完整小植株。结果表明在本试验条件下,不同长度的幼穗在培养时,其愈伤组织发生的部位及其增殖速度不同;4种材料愈伤组织诱导率和分化率无明显差异,均可有效诱导愈伤组织并分化成再生植株,再生植株的产生主要通过直接器官发生途径。     

苎麻悬浮细胞原生质体培养再生植株

苎麻品种浏阳大叶绿的子叶在含有２，４－Ｄ０．５ｍｇ／Ｌ、ＫＴ０．５ｍｇ／Ｌ的ＭＳＢ固体培养基上，形成愈伤组织。愈伤组织经３￣４次继代培养后作液体振荡培养，产生悬浮细胞系。从悬浮系分离的原生质体，只有以海藻酸钠包埋方式培养在ＫＭ８Ｐ培养基中，５０天左右才能形成肉眼可见的小愈伤组织。该愈伤组织在附加２，４－Ｄ０．２ｍｇ／Ｌ、６－ＢＡ０．１ｍｇ／Ｌ的ＭＳＢ生长培养基上增殖，然后转入附加６－ＢＡ２．０ｍｇ     

人工合成甘蓝型油菜高频率再生研究初报

资源材料保存在作物遗传资源的研究与利用中起到非常重要的作用。该实验以不同来源的人工合成甘蓝型油菜KH106，KH109，KH111D为材料，以花序轴，子房，果柄为外植体研究其再生情况，结果表明，由芥蓝和小白菜人工合成的甘蓝型油菜KH106的再生频率极显著高于由羽衣甘蓝和白菜型油菜人工合成的甘蓝型油菜KH109和KH111；与花序轴和子房为外植体再生频率相比，以果柄为外植体平均再生频率最高，差异达到极显著水平；利用不同预处理培养基处理不同时间，结果显示不经过预处理直接接种到分化培养基上再生频率最高。     

陆地棉（G．hirsutumL．）茎尖分生组织培养及其在基因导入上的应用

陆地棉栽培品种的种子无菌发芽１～３天。将萌动种子的顶端分生组织培养在无激素或附加低浓度激素ＭＳ基本培养基上，直接再生完整小植株。从顶端分生组织到再生植株所需的最短培养时间约１０天。顶端分生组织供体种芽的萌芽天数及其所连接的胚轴长度对植株再生频率有明显影响，但与品种的关系较小，不同品种均能获得再生植株。应用基因枪轰击法将ＣＰＴⅠ基因和ＮＰＴⅡ基因的重组质粒导入到棉花茎尖分生组织，培养获得卡那霉素抗性株。     

Continuous Plant Regeneration from Established Embryogenic Cell Suspension Cultures of Italian Ryegrass and Tall Fescue

The suitability of different protocols was compared for entire plant regeneration by somatic embryogenesis, of the forage plants Lolium multiflorum Lam. (Italian ryegrass) and Festuca arundinacea Schreb. (tall fescue). In the first protocol, miniature embryos were used as starting material, while mature seeds were retained in the other two. Whichever the considered protocol, undifferentiated calli were produced on Murashige and Skoog MS medium supplemented with 2,4-D. The calli were subcultured in the dark on solid MS agar medium, containing 5 mg/1 2,4-D (protocol 2) or on solid MS medium followed by transfer to a rotated liquid MS medium with 2 mg/1 2,4-D (protocol 1). In these conditions, induction of somatic embryogenesis occurred, and whole plants were regenerated during a limited lapse of time, upon transfer in the light, to MS medium supplemented with BAP but devoid of 2,4-D. The simultaneous elimination of 2,4-D and transfer to light appeared essential for full regeneration of the plants. Using this characteristic, an additional step was added to a new protocol (protocol 3) in which microcalli, cultured on liquid MS medium containing 5 mg/1 2,4-D, were transferred to the same medium with 2 mg/1 2,4-D, in the dark. In these conditions, the suspensions kept their embryogenic potential for months. In all cases, plantlets were successfully transferred into the soil. An evaluation of the somaclonal variation potential of the plants issued from each protocol is now underway.     

Genotypic differences in organogenesis from callus of ten triticale lines

Summary Callus was obtained from immature excised embryos of triticale using MS medium supplemented with 3 mg/l 2,4-D and 1 mg/l kinetin. The presence of 2,4-D was essential for continued callus proliferation. Plantlets were induced from the calli by sub-culturing on medium either devoid of auxin or containing 0.1 mg/l 2,4-D. The capacity to produce callus and to form organs and plantlets differed markedly among the genotypes used. Lines also had distinct response to presence and absence of 2,4-D in the regeneration media. The callus of most triticale lines used differentiated into organs more readily on MS medium supplemented with 0.1 mg/l 2,4-D than on medium without growth regulators. Very high frequencies (up to 75%) of plantlet regeneration were observed in several of the triticale lines studied.