温室网纹甜瓜发育模拟模型研究

 通过研究甜瓜的发育生理生态过程, 建立了以生理发育时间为基础的温室甜瓜发育过程模拟模型, 并利用不同播期、地点和品种的试验资料对模型进行了检验。结果表明, 模型对发芽期、幼苗期、伸蔓期、开花期、结果期等各生育期及全生育期的模拟预测值与实际观测值的符合度较好, 其回归估计标准误差(RMSE) 分别为1、3、2.2、1.8、1.1、2.6 d。     

利用RAPD和同工酶研究中国兜兰属种间亲缘关系

 本文选择14种10个碱基的寡核苷酸引物和7种酶系统, 应用RAPD和同工酶分子标记技术分析中国兜兰属(Paphiopedilum) 种间亲缘关系, 并与陈心启和Cribb的传统分类、Cox等的ITS结果进行比较。研究结果显示, RAPD和同工酶两种手段对种间亲缘关系的划分与传统分类大致吻合, 同工酶比RAPD的结果更接近传统分类。兜兰亚属需进一步分组, 彩云兜兰、卷萼兜兰、紫纹兜兰及其变种云南虎皮应自成一个组。     

几种植物提取物和药剂对桃蚜和萝卜蚜生长发育的影响

研究了苍耳提取物和合果芋(白蝴蝶)提取物以及常用天然药剂机油乳剂和 0. 3 %印楝素乳油对桃蚜和萝卜蚜实验种群的影响,两种提取物和药剂对桃蚜一龄若蚜的影响依次为: 0 3 % 印楝素乳油 (2 000×) >苍耳提取物(DW 0 04g·mL-1 ) >机油乳剂(400 ×) >白蝴蝶提取物(DW 0 04g·mL-1 ),对萝卜蚜一龄若蚜的影响依次为: 0. 3 %印楝素乳油(2 000×) >机油乳剂 ( 400×) >苍耳提取物 (DW 0. 04g·mL-1 ) >白蝴蝶提取物(DW 0. 04g·mL-1 );苍耳提取物对萝卜蚜实验种群有明显干扰控制作用,处理后萝卜蚜下代的种群增长量仅为对照的 24. 9 %;此外,苍耳提取物可延缓桃蚜和萝卜蚜的生长发育进程,使发育历期延长,对桃蚜的作用效果比对萝卜蚜的作用效果强;白蝴蝶提取物对萝卜蚜的实验种群也有一定的干扰作用,并可延长桃蚜的发育历期。     

无土栽培循环营养液的灭菌

与传统的土壤栽培方式相比,无土栽培的优点在于既可以生产廉价的无公害、绿色食品以满足人们的生活需要,又可向高精尖的方向发展,提高农产品的种植密度以提高产量,甚至可以满足航天、极地条件下的农作物生产的需要,所以无土栽培的发展前景不可估量.近年来,我国的无土栽培面积迅速增加,2000年达到500 hm2(公顷),2002年达到了856 hm2(公顷).     

台湾青枣不同品种花粉萌发和生活力测定

以5个台湾青枣品种盛花期花粉为试材，应用正交试验测定不同品种花粉萌发率及适宜的萌发条件，并用4种不同方法测定花粉生活力。结果表明：（1）不同品种的花粉萌发率存在显著差异，其中大世界的花粉萌发率最高。（2）硼酸浓度、培养温度等因素对花粉萌发率有极显著影响。最适培养基为含琼脂1％、蔗糖15％、硼酸0．02％的组合，适宜温度为30—32℃。（3）花粉生活力的测定中，离体萌发法是最佳选择，I—KI染色法、醋酸洋红染色法和TTC染色法不适宜用作台湾青枣花粉生活力的测定。     

壳寡糖与草莓细胞结合过程的研究

 壳寡糖是一类能有效的诱导植物抗病性的重要激发子。本研究用2 - 氨基吖啶酮(22AMAC)标记壳寡糖, 应用激光共聚焦显微成像技术, 研究了壳寡糖与草莓细胞结合过程。结果表明壳寡糖能通过草莓细胞壁与细胞膜结合, 在细胞壁和细胞膜上有其结合位点, 与壳寡糖的结合具有专一性。     

黑鹳F2的人工孵化及育雏的研究

2001～2004年在齐齐哈尔市龙沙公园对黑鹳F2的5只雏鸟的人工孵化温度和湿度进行记录。并对人工育雏成活的雏鸟的一系列生长指标如：体重、体长、喙长、翅长、跗跖长和尾长等进行测量，探讨黑鹳体长、体重等生长指标生长变化规律。结果表明：黑鹳卵的前中期（1～29d）孵化温度为37．7℃，湿度为55％，后期（29～31d）出雏温度为37℃，相对湿度65％；育雏箱的温度前7d为37℃，以后以每天0．5℃幅度逐渐降低，箱内湿度保持在55％，20日龄后可在室温下饲养；黑鹳F2雏鸟各生长指标的增长呈Logistic曲线。     

利用游离小孢子培养育成早熟大白菜新品种‘豫新5号’

 ‘豫新5号’是采用游离小孢子培养双单倍体育种技术选育的一代杂种，该品种生育期60 d，单球质量23 kg，球形指数1.35，高抗病毒病、霜霉病和软腐病，净菜产量56.7 t·hm^-2，可兼作早熟、晚熟栽培。     

Sca-1+ cells from mouse fetal liver can differentiate into neurons in vitro

AIM: To study whether Sca-1⁺ cells from fetal liver can be induced to differentiate into neuronal cells in vitro. METHODS:Sca-1⁺cells from 14 5-days-old murine fetal liver were isolated with a magnetic cell sorting kit, and were cultured in Dulbecco s modif ied Eagle s medium(DMEM)/F12 supplemented with 10%fetal bovine serum(FBS), and passaged at a rat io of 1 3 when cells reached more than 80%confluence.The 5 passage cells were induced by 10^-3mol/Lβ-mercaptoethanol(β-ME)and 5×10^-7 mol/L all-trans-retinoic acid(RA)for 24 hours, and then incubated in serum-free medium for 5 hours to 5 days.The characteristics of treated cel s were assayed by immunocytochemistry staining analysis at 5 hours, or 5 days.RESULTS: Cells treated with β-ME and RA exhibited neuronal phenotype and expressed neuron-specific protein such as neuron-specific nuclear protein (NeuN), neuronfilament-M, and neuron-specific tubulin-1 (TuJ-1) but not tau, MAP-2, or the astrocyte-specific marker glial fibrillary acidic protein (GFAP).CONCLUSION: Sca-1⁺ cells from fetal liver, of which most are regarded as hematopoietic stem cells, could differentiate into early immature neuronal cells in vitro. These findings suggest that Sca-1⁺ cells from fetal liver may be an alternative source in cell therapy and gene therapy of neural dysfunction.     

The transdifferentiation of Sca-1+ cells from murine fetal liver

AIM:To explore transdifferentiation potential of Sca-1⁺ cells from murine fetal liver. METHODS:2×10³ of Sca-1⁺ cells from male murine fetal liver were transfused into female mouse irradiated lethally with γ ray from ⁶⁰ Co source (10 Gy) via tail vein. Two months later, FISH and immunohistochemistry were used to detect the situation for transdifferentiating of the donor cells (male cells) in tissues of female recipient mouse. RESULTS:The renal tubular epitheliocyte-like and neurocyte-like cells with Y chromosome were found on the sections of renal and brain tissues from female recipient mice. These cells have phenotype characteristics of RCA⁺/CD₄₅^-F_4/80^- and NueN⁺/CD₄₅^-F_4/80^-, respectively. CONCLUSION:The evidence is provided for Sca-1⁺ cells from murine fetal liver to transdifferentiate into both renal and brain tissue cells.