CA贮藏对新鲜石刁柏的影响

用9种不同的CA条件与低温空气贮藏进行比较,结果证明用CA贮藏法进行石刁柏的贮藏保鲜是可行的。在设定的10个试验区中,当O_2浓度保持在21％的前提下,适当提高CO_2的浓度可提高贮藏效果。以21％O_2,30％CO:_2的贮藏条件保鲜效果较好。当CO_2浓度为0％时,O_2的浓度在1～0％之间保鲜效果最好。在10个试验区中,以空气条件下贮藏效果最差。     

贮藏温度和包装方式对红富士苹果贮藏效果的影响

以红富士苹果为试材,分别于0℃和冰温条件下,研究了不同包装材料及保鲜剂对红富士苹果采后贮藏保鲜期间品质变化的影响。结果表明,在冰温条件下,"微孔保鲜袋+高效乙烯吸收剂"和"保鲜袋+化学吸收剂"2种贮藏方式效果最好,延缓了果肉硬度及可溶性固形物(TSS)的下降速率,贮藏8个月仍能保持良好的品质。     

联合气调包装贮藏对樱桃保鲜效果的影响

采用冷藏条件下联合自发气调包装(CMP)方式贮藏樱桃进行了调查研究,结果表明,贮藏10天樱桃的呼吸强度为4.1 mgCO2/kg·h左右,腐烂率基本控制在10%以内.与纯冷藏相比,联合气调包装保鲜方式可以有效地降低采后樱桃的呼吸强度与腐烂率,有效地保持了采后樱桃的硬度,提高其耐贮性,经济效益显著.     

蘑菇低温气调保鲜的初步研究

采用正交实验方法，探讨了NaCl浓度、护色时间及控制贮藏环境温度等3个因素对蘑菇子实体的开伞率、PPO酶活变化量及ADF质量分数的影响。结果表明，蘑菇经适当处理，可有效抑制其开伞和品质变化。采用均匀试验设计回归分析程序对实验结果进行拟合，得到以蘑菇开伞率、PPO酶活变化及ADF质量分数为因变量，3个因素的水平编码号为自变量的回归方程估计值与实测值吻合。相对于单纯低温保鲜，采用低温气调保鲜的蘑菇，其品质和理化指标更为理想。     

鲜切苹果自发气调包装研究

以低密度聚乙烯、高密度聚乙烯、聚丙烯膜为包装材料,研究其对鲜切苹果的保鲜效果。结果表明:3种保鲜膜包装均能不同程度地抑制鲜切苹果呼吸强度,推迟呼吸高峰期到来,减少营养物质消耗,0.04mmLDPE保鲜膜较适合于鲜切苹果的自发气调包装。     

Reciprocal recurrent selection for multitrait indices in maize

Summary Reciprocal recurrent selection was carried out with two populations of maize (Zea mays L.) having good combining ability. We selected for higher grain yield, early maturity, shorter plant height and lodging resistance. Two cycles were completed in two years (four seasons), by resorting to late planting of S1 lines for recombination in the main season in which top-cross families were assessed. Top-crosses and selfings were made in the off-season. The original and improved versions of the populations and their crosses were evaluated in multilocation trials. The superiority of the population hybrid was 10.3% for grain yield, 5.5% for plant height and 1.8 days to silk. The improved hybrid had delayed leaf senescence and better resistance to lodging and post-flowering stalk rots. Among the yield components, only ear girth showed improvement. Syn 2 of the improved population cross showed a yield reduction of 6.2% in comparison to Syn 1. Intrapopulation gains were not significant except for lodging resistance in one population.     

包装对龙眼果实贮藏期间果皮失水褐变和细胞超微结构的影响

研究了(10±1)℃和50%相对湿度贮藏条件下无包装和0.015 mm厚的聚乙烯薄膜袋密封包装的“福眼”龙眼果实果皮失水、果皮褐变和细胞超微结构变化。结果表明，无包装的龙眼果实采后极易失水导致果皮迅速褐变，且褐变随贮藏时间的延长和果皮失水率的增加而升高，果皮褐变指数与果皮失水率呈极显著正相关(P<0.01)。在龙眼果皮失水褐变过程中，果皮细胞的细胞器和膜系统的完整性受到严重的破坏。而聚乙烯薄膜袋密封包装则显著减少了果皮失水和抑制果皮褐变，并保持较好的果皮细胞的细胞器和膜系统的完整性。据此认为，聚乙烯薄膜袋密封包装抑制龙眼果实失水果皮褐变与其维持细胞器和细胞膜的完整性有联系。     

猪卵母细胞在不同条件下的体外成熟培养

研究了不同时间段添加外源激素及不同基础培养液和血清有无对猪卵母细胞体外成熟的影响。实验包括（1）猪卵母细胞以TCM199＋10％FBS＋10IU／mL pregnant more serum gonadotrophin（PMSG）＋10IU／mL human chorion gonadotrophin（hCG）＋2．5IU／mL follicle stimulate hormone（FSH）为成熟培养液体外培养44h，前22h在培养液中加激素，后22h不加激素及前22h不加激素，后22h添加激素和添加激素连续培养44h；（2）以实验（1）中激素添加的方案在体外添加激素连续培养44h，对不同基础培养液（TCM199粉剂、TCM199原液和改良TCM199（mM199））对猪卵母细胞体外成熟进行了研究；（3）以实验（2）中筛选出的mM199组为成熟培养液对比血清有无对猪卵母细胞体外成熟的影响。结果表明，实验（1）中3种激素添加不同时间段其成熟率分别为45．67％、45．29％和46．07％，对猪卵母细胞体外成熟无显著影响（P〉0．05）；实验（2）中，mM199组的成熟率（54．10％）高于TCM199粉剂组的成熟率（46．16％）及TCM199原液组的成熟率（47．14％），但差异不显著（P〉0．05）；实验（3）中无血清组的成熟率（67．10％）高于有血清清组的成熟率（52．22％），差异显著（P〈0．05）。由此表明，mM199＋10IU／mL PMSG＋10IU／mL hCG＋2．5IU／mL FSH是一种适合于猪卵母细胞体外成熟的培养液，体外成熟率达67．10％。     

乙烯分解纳米光催化反应器关键性能参数研究

果品与蔬菜在采后贮藏过程中所产生和释放的乙烯是加速成熟、衰老和腐烂的重要环境因子。该研究采用纳米光催化技术开发设计了一种可以去除气调库中乙烯的玻璃管光催化反应器，并对其主要性能参数进行了模拟测试与分析。结果表明：气体流量、玻璃管直径与长度以及光源种类均是影响光催化反应器乙烯分解性能的主要因素。在该试验条件下，气体流量在40～80 L/h的范围内较佳；玻璃管的适宜内径为50 mm；在相同功率条件下黑光灯的光催化效果优于紫光灯。光催化反应器可以多级串联使用，以便提高系统的乙烯分解能力。这些研究结果为气调库用光催化乙烯分解装置设计提供了基础设计参数和指标。     

Suppression of root-knot disease by Pseudomonas fluorescens CHA0 in tomato: importance of bacterial secondary metabolite, 2,4-diacetylpholoroglucinol

The antimicrobial metabolites 2,4-diacetylphloroglucinol (2,4-DAPG) and pyoluteorin contribute to the ability of Pseudomonas fluorescens strain CHA0 to control plant diseases caused by soil-borne pathogens. P. fluorescens strain CHA0 and its derivatives CHA89 (antibiotics-deficient) and CHA0/pME3424 (antibiotics overproducing) were investigated as potential biocontrol agents against Meloidogyne javanica the root-knot nematode. Exposure of root-knot nematode to culture filtrates of P. fluorescens under in vitro conditions significantly reduced egg hatch and caused substantial mortality of M. javanica juveniles. Nutrient broth yeast extract (NBY) medium amended with 2% (w/v) glucose or 1 mM EDTA markedly repressed hatch inhibition activity of the strain CHA0 but not that of CHA0/pME3424 or CHA89. On the other hand, NBY medium amended with glucose significantly enhanced nematicidal activity of the strain CHA0/pME3424. Neither glucose nor EDTA had an influence on the nematicidal activity of the strains CHA0 and CHA89. Under in vitro conditions, antibiotic overproducing strain CHA0/pME3424 and CHA0 expressed phl‘-’lacZ reporter gene but strain CHA89 did not. Expression of the reporter gene reflects actual production of DAPG. In general, CHA0/pME3424 expressed reporter gene to a greater extent compared to its wild type counterpart CHA0. Regardless of the bacterial strains, reporter gene expression was markedly enhanced when NBY medium was amended with glucose but EDTA had no such effect. A positive correlation between the degree of juvenile mortality and extent of phl‘-’lacZ reporter gene expression was also observed in vitro. Strain CHA0 produced zones of 4-6 mm on MM medium containing gelatin while strain CHA0/pME3424 and CHA89 did not. When MM medium containing gelatin was amended with 2% glucose of 1 mM EDTA size of haloes produced by the strain CHA0 reduced to 2 mm. Under glasshouse conditions aqueous cell suspension of the strains CHA0 or CHA0/pME3424 at various inoculum levels (10⁷, 10⁸ or 10⁹ cfu ml⁻¹) significantly reduced root-knot development. CHA89 caused significant reduction in galling when applied at 10⁹ cfu ml⁻¹. To better understand the mechanism of nematode suppression, split root bioassay was performed. Split-root experiments, that guarantee a spatial separation of inducing agent and a challenging pathogen, showed that soil treatment of one half of the root system with cell suspension of CHA0 or CHA0/pME3424 resulted in a significant systemic induced resistance leading to reduction of M. javanica infection of tomato roots in the non-baterized nematode treated half. The results clearly suggest that the antibiotic 2,4-DAPG from P. fluorescens CHA0 act as the inducing agents of systemic resistance in tomato roots. Populations of CHA0 and its derivatives declined progressively by 10-fold between first and fourth harvests (0-21 days after inoculation). However, bacterial populations increased at final harvest (28 days after application).