以电导法配合Log istic方程确定茶梅‘小玫瑰’的抗寒性

 摘　要: 以不同处理时间、不同低温处理下茶梅‘小玫瑰’叶片的电解质外渗率(REC) 变化作曲线,并结合Logistic方程分别计算茶梅的半致死温度(LT50 ) , 结果发现在低温处理6 h以上, 茶梅叶片的REC均随着处理温度的降低而呈“S”形上升, 由此计算出“S”形拐点对应的温度即为茶梅叶片的LT50 , 其温度值在- 1215℃至- 14℃之间, 这可认为是茶梅抗寒能力的重要指标。关键词:     

花椰菜新品种———津品55

 ‘津品55’为秋中早熟花椰菜一代杂种, 成熟期约60 d, 内叶合抱护球, 花球较紧, 洁白,单球质量1.0 kg左右, 产量30000 kg/hm² 左右, 比对照品种‘丰花60’增产26.0% ～43.3% , 生长势强,抗病性好。     

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。     

杨桃果实生长发育过程中营养品质的变化

杨桃（Averrhoa arambola L．）为华南地区重要的热带水果。本试材为华南农业大学园艺分场种植的3年生盆栽马来西亚甜杨桃，砧木为酸杨桃。在杨桃的开花期，选择生长势、开花数量和时间较一致45株为试材，再选择受精时间一致的果实做标记。采样时问从开花后（2003年7月15日）至杨桃充分成熟（2003年10月25）。测定杨桃果实中的糖（蒽酮比色法）、有机酸（HPLC法）、维生素C（2，6-二氯靛酚钠滴定法）和单宁（高锰酸钾滴定法）的含量。     

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).     

黑穗醋栗新品种‘甜蜜’

 ‘甜蜜’是从波兰引进的黑穗醋栗试材中筛选出来的晚熟品种, 生长势强, 果穗长, 单果质量1.47 g, 可溶性固形物14% , 维生素C 1.6 g/kg FM。果实出汁率70%。风味酸甜, 鲜食口味佳。丰产性好。在长春地区7月中下旬成熟。     

嫁接西瓜肥料试验初报

试验结果表明,在土壤有机质含量高达4.07%的单栋钢管大棚中,进行嫁接西瓜栽培时,与常规施肥量相比,在4个减肥处理中,以减量20%的处理增产优质效果最佳。     

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.