黄花菜胚囊受精前后的超微结构观察

 应用透射电镜技术研究黄花菜（Hemerocallis citrine Baroni）助细胞、卵细胞、中央细胞、 合子与初生胚乳核的超微结构特征。结果如下：助细胞有高度发达的丝状器;一个助细胞在花粉管进入 后退化;宿存助细胞在合子期退化。受精前,卵细胞、助细胞合点端无壁,细胞膜完整;受精后,合子 被完整的细胞壁包围。受精前超微结构特征显示卵细胞代谢活动低,合子期的代谢活性被激活;中央细 胞、初生胚乳核代谢活性较高。卵细胞质中的精核由双层核膜包被,染色质高度凝聚,核孔数少。助细 胞、卵细胞、中央细胞缺乏中央大液泡是黄花菜成熟胚囊的显著特征。     

两系杂交油菜早中熟组合精量直播栽培性状比较研究

开展优质核不育两系杂交油菜早中熟新组合比较试验,结果表明:2种熟期类型杂交组合间产量差异明显,中熟组合单位面积产量极显著高于早熟组合,对比分析产量构成因子,主要是平均角粒数多和千粒重重,2种熟期类型组合间株高和一次分枝数差异较小,油菜菌核病感病程度中熟组合相对较轻。因此,油菜生产不可一味选择和使用早熟类型品种或组合,不然将较难获得理想产量和生产效益。     

小麦异源细胞质对主要病害抗性影响的初步研究

在大田自然发病和人工诱发条件下,研究了小麦异源细胞质对条锈、叶锈、秆锈、白粉和赤霉5种主要小麦病害抗性的影响。结果表明在同核条件下,不同异源细胞质对同一病害抗(感)性的影响不同,同一种细胞质对不同病害抗(感)性的影响也不完全相同;并且在不同地区试验的结果有时也有差异。根据初步研究结果,无芒山羊草、拟斯卑尔脱山     

偏型、粘型和易型小麦雄性不育系的初步研究

调查了10种不同山羊草(Aegilops)细胞质的异质小麦品种 Chris 与1B /1R 小黑麦易位系77(2)杂交 F_1及回交后代的育性表现,结果表明:1.在同核背景下,山羊草不同种的细胞质在对77(2)的育性反应上明显不同,依此差异进行特定的质核组配,能得到更宜于培育杂种小麦的新型不育系;2.不同的不育胞质在同核背景下虽都能产生雄性不育,但     

中国高粱细胞质对杂种一代的影响

采用中国高粱(麦茬)、迈罗及粒用草原1号三个不同细胞质的高粱雄性不育系,经过核置换,转育成为两套同核异质的6个高粱雄性不育系,并分别与同一个恢复系杂交得到两套共6个同核异质杂交种,以此为试材,观察了各个杂种一代的主要性状。结果表明,在生育天数、自交结实率、产量、千粒重、株高和叶片数等性状上,中国高粱细胞质与迈罗细胞质在相同的核背景下无显著差异。     

葡萄双受精过程的形态学观察

观察了葡萄双受精过程中雌雄性核的融合。结果表明:花粉管通过珠孔穿入退化助细胞,释放出二精子;精子核接近并贴附在卵核和次生核上,二者核膜融合,精核沉入卵核及次生核,染色质松解,并与雌性核染色质融合,出现雄性核仁,两性核仁融合,形成合子及初生胚乳核。卵核完成受精较次生核晚。受精属有丝分裂前型。精核进入卵核前看到了它的核仁。少数胚囊具有两套卵器。     

Effects of hypothalamic supraoptic ADH neurons at different times after hypophysectomy in Wistar rats

AIM:To observe the effects of supraoptic ADH neurons and central diabetes insipidus (CDI) in Wistar rats at different times after hypophysectomy.METHODS:Hypophysectomy was undergone by stereotaxic instrument.Water intake,urine output and urine specific gravity (SG) were observed each day.The survival rate of supraoptic ADH neurons was determined by immunofluorescence after hypophysectomy at different times.RESULTS:The rats manifested triphasic CDI after hypophysectomy.The average water intake in experiment group was 73.9 mL vs 30.9 mL in control group (P<0.01).Urine output was 59.7 mL vs 14.7 mL (P<0.01) and SG was 1.015 vs 1.036 (P<0.01).There was minor decrease in ADH neurons at the 3rd day after hypophysectomy (survival 94%,P>0.05),but the cellular body hypertrophy appeared.The survival rate at 10th day was 72％(P<0.01),31% at 20th day and 29% at 30th day.There was no difference between the 20th and 30th day (P>0.05),but they were all less than the 10th day (P<0.01).The ADH immunoreactivity enhanced in median eminence (ME) at the 20th day.CONCLUSION:The triphasic CDI appeard and supraoptic ADH neurons degenerated but the function of those survival neurons had compensatory enhancement after hypophysectomy.     

Effect of hypothalamic arcuate nucleus damaged by monosodium glutamate on bone histomorphometry parameters in rat

AIM: To investigate the effect of hypothalamic arcuate nucleus(ARC) damaged by monosodium glutamate (MSG) on bone histomorphometry parameters in rats. METHODS: (1) Newborn SD rats of experimental group were hypodermically injected 10% MSG (4 g/kg BW) on the postnatal lst, 3rd, 5th, 7th, 9th day. Meanwhile, the newborn rats of the control group were given equal volume of normal saline and the rats after the postnatal 70th, 72th, 74th, 76th and 78th day were hypodermically injected 10% MSG (4 g/kg BW) as the MSG toxicity control group. After survivial for 160 days, all rats were killed. (2) Morphological methods were used to estimate the ARC neurons and the bone histomorphometry parameters. (3) Radioimmunoassay was used to measure the levels of the serum growth hormoen(GH), estradiol(E2) and testosterone(T). RESULTS: The number of the hypothalamic arcuate nucleus neurons, the levels of serum E2, T, GH and the %Tb·Ar, Tb·Th, Tb·N of proximal tibial metaphysis(PTM) significantly decreased, while Tb·Sp of proximal tibial metaphysis(PTM) significantly increased, and the osteoporotic alterations appeared obviously. All these changes did not appear in the rats of NS group and MSG toxicity control group. CONCLUSION: (1) The changes of the bone in MSG guoup rats are not the effect of the MSG toxicity on the bone directly. (2) The hypothalamic arcuate nucleus participates in the regulation of the bone metabolism. (3) ARC regulates bone metabolism via altering the functions of the hypothalamus-GH-IGF-1 axis and the hypothalamus-pituitary-gonal axis.