马铃薯杂种F1的SSR鉴定

为选育抗黑痣病、高产优质的马铃薯新品种,选用引进品种‘大西洋’分别与‘陇薯6号’、‘陇薯7号’杂交,获得了杂种F1代,利用SSR标记技术对‘大西洋’与‘陇薯6号’的42个杂种F1、‘大西洋’与‘陇薯7号’的9个杂种F1单株进行了鉴定。从59对SSR引物中筛选出2对在亲本间存在差异、扩增稳定、条带清晰的引物S184和STM1049,用于‘大西洋’ב陇薯6号’杂种F1、‘大西洋’ב陇薯7号’杂种F1及其亲本的基因组DNA扩增。SSR带型分析显示,杂种F1的SSR带型呈双亲互补型、缺失型、父本型和母本型4类,依据带型特征鉴定出供试的51个马铃薯杂种F1单株均为真杂种,表明SSR分子标记技术用于马铃薯杂种真实性鉴定是可行的。该研究可为进一步开展马铃薯杂交后代目标性状优异株系选育提供依据。     

3个马铃薯杂种优良株系的核型及SSR分析

为明确‘费乌瑞它’ב陇薯3号’杂种F1优良无性株系A1和A3及‘费乌瑞它’×J07-6杂种F1优良无性株系C2在染色体及DNA水平上的遗传差异,利用根尖染色体制片技术和SSR分子标记技术,对这3个优良株系的核型及SSR指纹特征进行分析。结果表明:(1)株系A1、A3和C2均为四倍体(2n=4x=48),其核型类型分别为2B、1B和1A;株系A1和A3核型公式均为2n=4x=48=36m+12sm,C2核型公式为2n=4x=48=48m。(2)利用筛选出的10对SSR适宜引物PCR扩增得到50个多态性位点,多态性位点百分率为79.37%。(3)建立了3个马铃薯杂种优良株系及其亲本的SSR指纹图,并以遗传距离(GD值)0.45为基准,将6个材料分为3类:母本‘费乌瑞它’、株系A1和父本‘陇薯3号’聚为一类,株系A3和C2聚为另一类,父本J07-6单独列为一类。     

长芒猬草与华山新麦草属间杂种的形态学和细胞学研究

为研究长芒猬草Hystrix duthiei ssp．longearistata的染色体组成,将其与华山新麦草Psathyrostachys huashanica进行了人工杂交,获得杂种F₁。对亲本及杂种F₁,花粉母细胞减数分裂染色体配对行为、繁育 特性和形态特征进行了比较分析。结果表明：杂种F₁的许多形态特征介于父母本之间,花粉完全不育, 结实率为0;杂种F₁花粉母细胞减数分裂中期Ⅰ染色体配对较高,55.12％的细胞形成5个或6个二价 体,其构型为：9.83Ⅰ+5.46Ⅱ+0.07Ⅲ,C-值为0.57。以上结果表明H．duthiei ssp．Longearistata含有Ns染色体组。本文还讨论了Hystrix与Leymus的关系。     

马铃薯杂种无性株系的SSR鉴定及花粉育性和染色体构型分析

为明确马铃薯‘MB09’ב陇薯7号’杂种F1无性株系在DNA和细胞遗传学水平上的差异,该试验以亲本材料为对照,利用SSR分子标记技术对其20个优良无性株系(F1无性系一代)的DNA指纹特征进行分析,并采用常规制片镜检方法对已选出的8个杂种优良株系(F1无性系二代)的花粉育性及花粉母细胞减数分裂中期Ⅰ(PMCMⅠ)的染色体配对构型进行了研究,为马铃薯杂交新品系选育提供分子细胞遗传学依据。结果显示:(1)试验共筛选出2对SSR特异引物C57和S25,通过PCR扩增建立了能识别出这20个杂种株系及其双亲的SSR指纹图。(2)杂种优异株系F1-1、F1-2、F1-7、F1-11、F1-13、F1-14、F1-15和F1-20的花粉可育率变幅为36.73%~87.08%,并以株系F1-7最高(87.08%),而且显著超过高亲(83.33%),说明各优良株系花粉育性有一定差异。(3)对8个优异株系花粉母细胞的PMCMⅠ观察发现,各优良株系的染色体配对构型明显不同,均包括单价体、二价体、三价体和四价体4类,其中二价体构型的比例最高,其介于49.13%~82.91%之间,其中以株系F1-7的二价体比例最高(82.91%)。该研究明确了20个马铃薯杂种优良株系的SSR指纹特征和8个优异株系的花粉育性及染色体配对构型差异。     

大气NH3浓度升高对不同氮效率玉米生理指标及生物量的影响

 该试验采用开顶式气室(Open top chambers)装置,在两种大气NH₃浓度水平(大气背景浓度值为10 nl&;#8226;L^－1和高NH₃浓度1 000 nl&;#8226;L^－1)和两种 供氮介质水平(高供氮介质和低供氮介质)下,对两种氮效率玉米(Zea mays)基因型(‘氮高效5号’(NE5)和‘氮低效四单19’(SD19))的叶绿素 指标值(SPAD值)、净光合速率(P_n)、气孔导度(G_s )、生物量和根冠比等生物学和生理学指标进行了测定。结果表明,大气NH₃浓度升高对两种 氮效率玉米基因型各生理指标有显著影响(p<0.05)。与大气背景NH₃浓度相比,当大气NH₃浓度为1 000 nl&;#8226;L^－1 时,生长在高供氮介质中‘氮 高效5号’的SPAD值、P_n和G_s分别降低7.0%、14.0%和6.5%,而‘氮低效四单19’的对应指标分别降低9.0%、11.0%和6.9%;生长在低供氮介质 中的两种氮效率玉米基因型各生理指标均显著增加(p<0.05)：‘氮高效5号’的SPAD值、P_n和G_s分别增加5.7%、7.1%和17%,‘氮低效四单19’ 的对应指标分别增加7.0%、11.0%和22.0%。高供氮介质中NH₃浓度升高对氮低效基因型玉米冠层生物 量抑制作用小于对氮高效基因型玉米的抑 制效应,而低供氮介质中NH₃浓度升高对氮高效基因型玉米冠部的促进作用显著高于对氮低效基因型玉米的促进作用(p<0.05);两种大气NH₃营 养下玉米根冠比的变化与采样时期有关。说明从大气中吸收NH3有利于改善生长在低供氮介质上玉米的氮素营养状况,而且对氮低效基因型玉米 的促进作用比对氮高效基因型玉米更加显著。     

浓度升高对不同氮效率玉米生理指标及生物量的影响

该试验采用开顶式气室(Open top chambers)装置,在两种大气NH₃浓度水平(大气背景浓度值为10 nl&#8226;L^－1和高NH₃浓度1 000 nl&#8226;L^－1)和两种 供氮介质水平(高供氮介质和低供氮介质)下,对两种氮效率玉米(Zea mays)基因型(‘氮高效5号’(NE5)和‘氮低效四单19’(SD19))的叶绿素 指标值(SPAD值)、净光合速率(P_n)、气孔导度(G_s )、生物量和根冠比等生物学和生理学指标进行了测定。结果表明,大气NH₃浓度升高对两种 氮效率玉米基因型各生理指标有显著影响(p<0.05)。与大气背景NH₃浓度相比,当大气NH₃浓度为1 000 nl&#8226;L^－1 时,生长在高供氮介质中‘氮 高效5号’的SPAD值、P_n和G_s分别降低7.0%、14.0%和6.5%,而‘氮低效四单19’的对应指标分别降低9.0%、11.0%和6.9%;生长在低供氮介质 中的两种氮效率玉米基因型各生理指标均显著增加(p<0.05)：‘氮高效5号’的SPAD值、P_n和G_s分别增加5.7%、7.1%和17%,‘氮低效四单19’ 的对应指标分别增加7.0%、11.0%和22.0%。高供氮介质中NH₃浓度升高对氮低效基因型玉米冠层生物 量抑制作用小于对氮高效基因型玉米的抑 制效应,而低供氮介质中NH₃浓度升高对氮高效基因型玉米冠部的促进作用显著高于对氮低效基因型玉米的促进作用(p<0.05);两种大气NH₃营 养下玉米根冠比的变化与采样时期有关。说明从大气中吸收NH3有利于改善生长在低供氮介质上玉米的氮素营养状况,而且对氮低效基因型玉米 的促进作用比对氮高效基因型玉米更加显著。     

普通小麦与鹅观草属间杂种F1及BC1的分子细胞遗传学、育性和赤霉病抗性研究

通过胚拯救, 成功获得鹅观草Roegneria kamoji (2n=6x=42, SSHHYY)和普通小麦中国春Triticum aesti-vum (2n=6x=42, AABBDD)的正反交属间杂种F1, 并对这些杂种F1及其BC1的形态学、减数分裂配对行为、育性和赤霉病抗性进行研究。结果表明, (鹅观草×中国春)F1和(中国春×鹅观草)F1的形态介于双亲之间。杂种F1花粉母细胞减数分裂中期I染色体构型分别为40.33I + 0.78II + 0.03III和40.40I + 0.79II 。杂种F1高度雄性不育, 用中国春花粉与其回交可获得BC1代种子。(鹅观草×中国春) F1×中国春BC1植株的染色体数目主要分布在55~63之间, 单价体较多, 植株高度不育; (中国春×鹅观草)F1×中国春BC₁植株染色体数目也主要分布在55~63之间, 但其中部分植株拥有整套小麦染色体且能正常配对、分离, 可形成部分可育花粉粒, 能收到少量自交结实种子。在 (鹅观草×中国春)F1中有1株穗型趋向中国春, 其染色体数目为2n=63, 经染色体分子原位杂交(GISH)检测, 含有42条小麦染色体和21条鹅观草染色体。该杂种F1在减数分裂中期I平均每个花粉母细胞有26.40I+18.30II, 但植株高度雄性不育, 用中国春花粉回交能收到BC₁种子。(鹅观草×中国春) F₁ (2n=63)×中国春BC₁的染色体数目主要分布在40~59之间, 其中的外源染色体已经逐渐减少, 虽然该BC₁的穗型已接近中国春, 但仍然高度不育。赤霉病抗性鉴定结果显示, 所有杂种F1及大部分BC₁对赤霉病均表现出较好的抗性。     

水杨酸对高温强光胁迫下小麦叶绿体D1蛋白磷酸化及光系统Ⅱ功能的影响

为了研究水杨酸（SA）对高温强光胁迫下小麦叶片类囊体膜D₁蛋白磷酸化和PSⅡ功能的影响,用0.5 mmol·L^-1 SA溶液预处理灌浆期小麦叶片,以水预处理为对照,然后将预处理植株进行高温强光（35 ℃,1 600 μmol·m^-2·s^-1）处理,测定胁迫处理过程中小麦旗叶光合电子传递速率、净光合速率、叶绿素荧光参数及D₁蛋白的变化.结果表明：SA预处理有效抑制了高温强光下D₁蛋白的净降解,保持了较高的D₁蛋白磷酸化水平、全链电子传递速率和PSⅡ电子传递速率,维持了较高的PSⅡ原初光化学效率（F_v/F_m）、实际光化学效率(Ф_PSⅡ)、光化学淬灭系数（q_P）和净光合速率（P_n）.表明外源SA通过调节小麦叶绿体D₁蛋白的周转,减轻了高温强光胁迫对叶片光合机构的损伤,有利于PSⅡ的正常运转.     

茶树SBP box转录因子的比较基因组学与遗传分析

SQUAMOSA启动子结合蛋白(SBP box)是植物特异性转录因子,在植物生长发育中发挥重要作用。该研究利用生物信息学分析方法,对不同‘铁观音’、‘黄棪’、‘舒茶早’和‘龙井43’茶树基因组的SBP基因进行鉴定和比较,通过qRT PCR技术分析CsTGY_SBP家族成员在不同茶树品种中的表达模式,为探究SBP基因在茶树杂种和亲本上的遗传规律提供参考。结果显示：(1)在茶树品种‘铁观音’、‘黄棪’、‘舒茶早’和‘龙井43’基因组中分别鉴定出21个、25个、24个和23个SBP家族基因。(2)系统进化树将其分为8个亚家族,共线性分析发现茶树和拟南芥、葡萄的SBP基因共线性关系与水稻相比更强,同物种内发现‘铁观音’与‘黄棪’的共线性关系更显著。(3)qRT PCR结果表明,CsTGY_SBP5、CsTGY_SBP9和CsTGY_SBP14在F₁‘金观音’中呈中亲表达的模式;大部分CsTGY_SBPs基因在F₁‘黄观音’呈低于双亲表达模式,CsTGY_SBP5和CsTGY_SBP8在F₁‘金牡丹’中显著高于亲本;CsTGY_SBP5、CsTGY_SBP7、CsTGY_SBP12、CsTGY_SBP16和CsTGY_SBP18在F₁‘紫玫瑰’中的表达量显著高于亲本,呈超高亲表达的模式;CsTGY_SBPs基因在F₁‘紫牡丹’中整体表达趋于亲本铁观音,在F₁‘瑞香’中整体呈现低于亲本‘黄棪’的表达模式。研究表明,CsTGY_SBP5在F₁‘金牡丹’和F₁‘紫玫瑰’中的表达均显著高于亲本,推测CsTGY_SBP5可能是茶树杂种优势的重要调控因子。     

甘肃定西地区主栽品种马铃薯颗粒全粉品质分析

以甘肃定西地区主栽的7个品种马铃薯为原料,采用微波工艺生产马铃薯颗粒全粉,并测定其原料品质指标（干物质、总淀粉、直链淀粉、还原糖、维生素C含量）和其颗粒全粉的功能指标（蓝值、持水性和持油性）。结果表明：除克新1号品种马铃薯的干物质含量偏低、还原糖含量较高以外,其余6个品种费乌瑞它、陇3、青薯6号、冀张薯8号、陇薯6号、庄薯3号均符合加工全粉的要求;马铃薯原料中总淀粉含量高,则游离淀粉的含量相对较高。7个品种马铃薯颗粒全粉的蓝值顺序为费乌瑞它>冀张薯8号>庄薯3号>青薯6号 > 陇薯3号>陇薯6号> 克新1号;持水性顺序为冀张薯8号>费乌瑞它>青薯6号>庄薯3号>陇薯3>陇薯6>克新1号;持油性高低顺序是克新1号>青薯6号>冀张薯8号>庄薯3号>陇薯3号>陇薯6号>费乌瑞它。该结果可为甘肃省定西地区马铃薯颗粒全粉生产的原料选择和颗粒全粉应用提供科学依据。     

穗花杉ISSR引物反应条件的优化与筛选

在研究穗花杉(Amentotaxus aragotaenia)的遗传多样性过程中,为了获得清晰、重复性好ISSR扩增结果,对影响ISSR-PCR的多个因素包括模板浓度、Taq酶的选择和用量、Mg²⁺和dNTPs浓度及退火温度等指标等进行了筛选和优化,确定了穗花杉ISSR-PCR分析的最适扩增条件： 20 μL PCR反应体系中,2 μL 10×Taq酶配套缓冲液,1.8 U Taq聚合酶（上海生工公司）,0.2 μmol·L^-1引物,0.18 mmol·L^-1 dNTP,1.5～2.5 mmol·L^-1 MgCl₂,10 ng·μL^-1模板DNA。用来自不同居群7个个体,以100个ISSR引物进行PCR扩增,筛选出扩增效果较好的10个引物。得到了92个位点,其中45个多态性位点,多态性位点比例为49%。     

Molecular Characterization of Brinjal (Solanum melongena L) Cultivars using RAPD and ISSR Markers

Molecular characterization of 19 advanced cultivars and landraces of brinjal was carried out using RAPD and ISSR markers. Twenty-nine RAPD primers generated a total of 240 amplified fragments, while 23 anchored and non-anchored ISSR primers produced 299 fragments. Of these, 66 (27.5%) RAPD and 56 (18.73%) ISSR fragments were polymorphic. All the cultivars could be distinguished based on RAPD and/or ISSR profiles. A set of two RAPD primers, OPW 11 and OPX 07, was adequate to distinguish all the 19 cultivars. On the other hand, a minimum of ten ISSR primers were required to achieve the same result. Eleven cultivars could be identified by the unique presence or absence of one to four markers. The correlation between primer Rp and the number of cultivars distinguished by RAPD was r = 0.873, while that for ISSR it was r = 0.327. The correlation between PIC of primer and the number of cultivars distinguished was r = 0.324 for RAPD, while for ISSR primers it was r = ? 0.066. The probability of chance identity between two cultivars for RAPD and ISSR markers was calculated as 8.94×10^?4 and 2.25×10^?2, respectively. The average Jaccard’s similarity coefficient between cultivars based on combined RAPD and ISSR data was estimated to be 0.919. The UPGMA analysis grouped the cultivars into three main clusters with significant bootstrap support. While the cultivars bred at Indian Agricultural Research Institute, New Delhi formed one sub-cluster; others did not show a prominent region-based clustering.     

DYNAMIC RESPONSE OF ROOT BORDER CELLS AND THEIR ASSOCIATED MUCILAGE EXUDATION IN SOYBEAN TO AI STRESS AND RECOVERY

 以耐铝性明显差异的两个大豆(Glycine max)基因型‘浙秋2号’(耐性)和‘浙春3号’(敏感)为材料, 研究根尖边缘细胞比活度、粘液分泌和根长对铝胁迫和解除胁迫的反应, 明确边缘细胞的粘液分泌对策在铝毒环境中的生态学意义。结果表明, ‘浙秋2号’在100~400 µmol&;#8226;L^–1 Al³⁺处理的3~12 h, 边缘细胞比活率呈递减趋势, 12 h后比活率又略有上升。‘浙春3号’在300和400 µmol&;#8226;L^–1 Al³⁺处理的变化与前者一致。两个大豆基因型的粘液层随着Al³⁺浓度增加和时间延长而增厚, 并于400 µmol&;#8226;L^–1 Al³⁺处理24 h时达到最大(>17 µm)。‘浙秋2号’在低浓度Al3+ (100和200 µmol&;#8226;L^–1)处理3~6 h后就会分泌大量粘液, ‘浙春3号’则在300 µmol&;#8226;L^–1 Al³⁺处理12 h后才有类似的变化。‘浙秋2号’在400 µmol&;#8226;L^–1 Al³⁺处理下的根相对伸长率均高于100~300 µmol&;#8226;L^–1 Al³⁺处理, ‘浙春3号’则表现为Al³⁺浓度越高, 根伸长受抑越明显。Al³⁺胁迫解除后, ‘浙秋2号’的粘液分泌速度和分泌量急剧下降, ‘浙春3号’在胁迫解除后的24 h, 仍会持续、大量地分泌粘液(>19 µm)。可见, 耐性大豆通过在铝胁迫初期快速、大量地分泌粘液以维持较高的边缘细胞活性和解除胁迫后迅速降低粘液的分泌速度及分泌量来适应铝毒害环境。     

Fiber yields inSansevieria interspecific hybrids

Fiber yields are reported for the interspecific hybrid ‘ Florida H-13’ (Sansevieria trifasciata Prain × S. deserti 2V. E. Brown), subjected to various harvesting cycles at three locations in southern Florida. Yields of ‘Florida H-13’ are compared with those of other F₁F₂triploid, and backcross hybrids and the parental species, S. trifasciata. Fiber yields were higher from plants grown on peat soil at Belle Glade than on sandy soil at Lake Worth or Immokalee, in spite of the significantly colder winters encountered at the former location. Average annual fiber yields at first harvest increased up to 30 months of age at Belle Glade and Lake Worth and up to 66 months of age at Immokalee. Re-growth yields were higher than original yields front plants grown at Belle Glade, sometimes higher from those grown at Lake Worth, but significantly lower from those grown at Immokalee. Annual harvests of ‘Florida H-13’ were neither feasible nor necessary, even though plants sustained frost damage each winter at Belle Glade and lmmokalee. None of the other hybrids yielded significantly more fiber than ‘Florida H-13’, but one F₁, clone, H52-151, and two triploid clones, H54-4 and H54-5, sometimes yielded as much. Results suggest that ‘Florida H-13’ could be grown successfully as a fiber crop in southern Florida, particularly on peat soils, where high yields would be associated with low fertilizer costs.     

An interstitial telomere array proximal to the distal telomere of mouse chromosome 13

Lambda clones of mouse DNA from BALB/c and C57BL/10, each containing an array of telomere hexamers, were localized by FISH to a region close to the telomere of Chr 13. Amplification of mouse genomic DNA with primers flanking SSRs within the cloned DNA showed several alleles, which were used to type eight sets of RI strains. The two lambda clones contained allelic versions of the interstitial telomere array, Tel-rs4, which is 495 bp in C57BL/10 and which includes a variety of sequence changes from the consensus telomere hexamer. Comparison of the segregation of the amplification products of the SSRs with the segregation of other loci in an interspecies backcross (C57BL/6JEi × SPRET/Ei) F₁× SPRET/Ei shows recombination suppression, possibly associated with ribosomal DNA sequences present on distal Chr 13 in Mus spretus, when compared with recombination in an interstrain backcross, (C57BL/6J × DBA/J) F₁× C57BL/6J, and with the MIT F₂ intercross. Analysis of recombination in females using a second interstrain backcross, (ICR/Ha × C57BL/6Ha) F₁× C57BL/6Ha, also indicates recombination suppression when compared with recombination in males of the same strains, using backcross C57BL/6Ha × (ICR/Ha × C57BL/6Ha) F₁. Thus, more than one cause may contribute to recombination suppression in this region. The combined order of the loci typed was D13Mit37–D13Mit30–D13Mit148–(D13Rp1, 2, 3, 4, Tel-rs4)–D13Mit53–D13Mit196–D13Mit77–(D13Mit78, 35). Data from crosses where apparently normal frequencies of recombination occur suggest that the telomere array is about 6 map units proximal to the most distal loci on Chr 13. This distance is consistent with evidence from markers identified in two YAC clones obtained from the region. Received: 24 September 1996/Accepted: 20 January 1997     

Expression of the nuclear gene TaF(A)d is under mitochondrial retrograde regulation in anthers of male sterile wheat plants with timopheevii cytoplasm

Alterations of mitochondrial-encoded subunits of the F_oF₁-ATPsynthase are frequently associated with cytoplasmic male sterility(CMS) in plants; however, little is known about the relationshipof the nuclear encoded subunits of this enzyme with CMS. Inthe present study, the full cDNA of the gene TaF_Ad that encodesthe putative F_Ad subunit of the F_oF₁-ATP synthase was isolatedfrom the wheat (Triticum aestivum) fertility restorer ‘2114’for timopheevii cytoplasm-based CMS. The deduced 238 amino acidpolypeptide is highly similar to its counterparts in dicotsand other monocots but has low homology to its mammalian equivalents.TaF_Ad is a single copy gene in wheat and maps to the short armof the group 6 chromosomes. Transient expression of the TaF_Ad–GFPfusion in onion epidermal cells demonstrated TaF_Ad's mitochondriallocation. TaF_Ad was expressed abundantly in stem, leaf, anther,and ovary tissues of 2114. Nevertheless, its expression wasrepressed in anthers of CMS plants with timopheevii cytoplasm.Genic male sterility did not affect its expression in anthers.The expression of the nuclear gene encoding the 20 kDa subunitof F_o was down-regulated in a manner similar to TaF_Ad in theT-CMS anthers while that of genes encoding the 6 kDa subunitof F_o and the subunit of F₁ was unaffected. These observationsimplied that TaF_Ad is under mitochondrial retrograde regulationin the anthers of CMS plants with timopheevii cytoplasm. Key words: CMS, F_Ad subunit, F_oF₁-ATP synthase, retrograde regulation, wheat Received 8 October 2007; Revised 9 January 2008 Accepted 28 January 2008     

Using SSR markers for hybrid identification and resource management in Vietnamese <Emphasis Type="Italic">Acacia</Emphasis> breeding programs

We used a set of 16 SSR markers to check the identity of pure-species and hybrid clones in Vietnam’s Acacia auriculiformis, Acacia mangium, and acacia hybrid (A. mangium × A. auriculiformis) breeding programs. The statistics package HIest, applied to a large synthesized population, enabled accurate allocation of genotypes to the two pure species, F₁ and F₂ inter-specific hybrids and backcrosses, based on estimates of hybridity and heterozygosity. The hybridity status of putatively pure A. mangium and A. auriculiformis clones in adjacent clonal seed orchards was checked. Four out of 100 clones selected as A. mangium were found to be backcrosses (A. mangium × F₁ inter-specific hybrid) while out of 96 clones selected as A. auriculiformis, two were F₁ hybrids and two were backcrosses (A. auriculiformis × F₁ hybrid). The markers were then applied to check the hybridity status of 160 putative acacia F₁ hybrid genotypes that had been selected on morphological criteria from open-pollinated progenies collected from A. auriculiformis and A. mangium parents. Many selections based on morphology were found to be mistaken. Only thirteen of 63 clones originating from A. auriculiformis mothers were F₁ hybrids, four were backcrosses, and the remaining 46 were pure A. auriculiformis. Fewer mistakes were evident for clones selected from A. mangium mothers, with 82 out of 89 clones confirmed as F₁ hybrids, three as backcrosses, and four as pure A. mangium. The occurrence of F₁ hybrids and backcrosses in pure-species seed orchards and their progeny shows that inter-species contamination is an issue requiring management in both pure-species and in hybrid breeding of these species in Vietnam. Examination of genetic distances among verified clones showed patterns of relatedness that were consistent with pedigree records. Implications for resource management as well as for breeding and clonal selection strategies are considered.     

FISH分析栽培高粱×拟高粱、甜高粱×拟高粱的染色体行为

采用荧光原位杂交技术对45S rDNA在栽培高粱×拟高粱、甜高粱×拟高粱F1的有丝分裂和减数分裂染色体进行定位研究。在有丝分裂中期染色体上2个杂种分别检测到2个杂交信号, 在减数分裂粗线期、终变期、中期Ⅰ染色体上45S rDNA位于一个二价体上, 说明这两个杂种携带45S rDNA的染色体为同源染色体。根据45S rDNA位点随细胞减数分裂过程的位置变化, 表明这两个杂种染色体配对行为正常, 平均构型为2n=2x=20(10Ⅱ), 证明45S rDNA可作为染色体的一个识别指标间接地观察细胞减数分裂过程染色体的变化行为。