不同包衣剂对直播稻苗期素质及产量的影响

通过选择市场上效果较好的包衣剂以及新推出的包衣剂,探究药剂包衣对直播稻秧苗素质及产量结构的影响.结果表明,多·咪·福美双处理可有效提高水稻出苗率、苗期根冠比及叶绿素含量,提高水稻秧苗素质,壮秧生长整齐,最终形成大穗,在同样栽培条件下,壮秧容易获得高产,即包衣剂处理可有效提高产量.     

耐低温耐低氧萌发野败不育系赣野A的选育

赣野A是江西省农科院水稻研究所将东乡野生稻的耐冷性和耐低氧萌发能力导入抗稻瘟病保持系赣香B后再与赣香A测交和回交育成的野败型三系籼稻不育系。该不育系败育彻底,异交结实率高,配合力较强,具有较强的耐冷性和耐低氧萌发能力,在直播杂交稻育种中应用前景广阔。2019年通过了江西省品种审定。     

Shikonin reverses HGF-induced resistance to gefitinib in lung cancer cells HCC827

AIM: To investigate the effect of shikonin on reversing hepatocyte growth factor(HGF)-induced resistance to gefitinib in lung cancer HCC827 cells, and to explore its possible mechanisms.METHODS: The gefitinib-resistant HCC827 cells induced by HGF were treated with shikonin and gefitinibthe alone or in combination. The inhibition rates of cell viability were determined by MTT assay. The invasive ability of HCC827 cells with HGF-induced resistance to gefitinib was determined by Transwell assay. The protein levels of epithelial-mesenchymal transition (EMT) and related signaling pathway in the HCC827 cells were detected by Western blot.RESULTS: The results of MTT assay showed that the cell activity of HCC827 cells was significantly inhibited by shikonin in a dose dependent manner. The IC₅₀ of shikonin in HCC827 cells was 3.06 μmol/L. And the IC₅₀ of gefitinib in HCC827 cells was 0.51 μmol/L. Under the condition of combined treatment with shikonin and gefitinib in the presence of HGF (20 μg/L), the IC₅₀ of gefitinib was 7.36 μmol/L, significantly lower than that treated with gefitinib alone (P<0.01), so did the result of the cell migration (P<0.01). HGF induced EMT, while shikonin reversed this effect. The protein expression level of p-AKT was significantly up-regulated by HGF, while markedly down-regulated treatment with shikonin and gefitinib compared with gefitinib alone (P<0.01).CONCLUSION: Shikonin reverses HGF-induced resistance to gefitinib in lung cancer HCC827 cells, and the mechanism may be likely related to the preventon of EMT and the inhibition of HGF-induced activation of p-AKT signaling pathway.     

梨三倍体新品种龙园洋红的选育

龙园洋红梨是梨三倍体新品种,亲本为56-520×乔玛,抗寒性强,短枝型.果实不规则长椭圆形,果形指数1.13,平均单果重185.5 g,每个果实平均2.5粒种子,种子小、不饱满,多畸形.果皮浅黄色,阳面有红晕,果肉乳白色,肉质细软多汁,风味甜,有香气,可溶性固形物16.05%.果实在哈尔滨地区9月中旬成熟.     

长安区城市森林建设思路探讨

本文探讨了如何在西安市近郊长安区发展城市森林,以适应西安现代国际化大都市建设发展的需要。     

大别山-桐柏山地区杀虫性植物资源调查初报

大别山、桐柏山属于亚热带向暖温带过渡地气候 ,是植物区系的交接过渡地带 ,既有亚热带典型的代表型 ,又体现着过渡性的特征。能产生具有杀虫活性的次生代谢产物的植物即杀虫性植物。通过广泛调查、采集与鉴定 ,大别山—桐柏山地区分布有杀虫性植物 72科 138种     

用RAPD技术筛选中国荷斯坦牛产奶量性状遗传标记

选用320条10碱基随机引物在由36头高产（305d产奶量〉8500kg）和32头低产（305d产奶量〈5600kg）中国荷斯坦牛所组成的2个DNA池间进行RAPD-PCR扩增，从中筛选出稳定性好、带型清晰且在2个DNA池间有明显差异的RAPD引物24条。用筛选到的24条引物对所有个体进行PCR检测，得到了5个与奶牛产奶量性状相关的RAPD标记，并对其中4个进行了克隆测序和SCAR标记转化以及生物信息学分析。结果表明：SCAR标记yield—s139与产奶量密切相关，应用电子克隆方法已将该标记由921bp延伸到2141bp，经同源性比较发现，此标记对应于奶牛基因组中LINEs家族中的一个重复元件，推测该元件附近可能存在与产奶量性状相关的QTLs或主效基因。     

葡萄子油及原花青素研究与开发利用

综述了葡萄子油、葡萄子原花青素等天然产物的提取与保健作用的研究进展,原花青素的生物活性及药理研究的现状,葡萄子油成分分析方法和葡萄子,提取物中原花青素含量测定的方法;介绍了用超临界CO2萃取法制取高质量的葡萄子油和应用夹带剂提取葡萄子中的原花青素的方法。分析了葡萄子的综合开发的应用前景。     

荔枝、龙眼园使用机油乳剂的安全性及其对荔枝蒂蛀虫的防治研究

利用机油乳剂对果树进行安全性和防治荔枝蒂蛀虫Conopomorpha sinensis Bradley研究试验，结果表明，喷施机油乳剂后荔枝和龙眼的落果率与对照树4无差异，喷清水的对照树其蒂蛀虫蛀果率比喷机油乳剂的处理树高，分别为150、200和250倍机油乳剂处理的2.8、3.0和2.7倍。在荔枝、龙眼园应用机油乳剂防治害虫不会导致落叶、落果、畸形叶和畸形果，也不会延缓果实的生长和成熟及降低单果重，而有利于控制介壳虫、螨类、蛀果类等害虫。机油乳剂可替代广谱性化学农药的使用，减少化学农药的污染，有利于果园天敌的生存、繁殖，提高生物多样性，改善果园生态环境。     

The genetic susceptibility of HLA-DRB1 alleles in esophageal neoplasm of Hubei Han Chinese

AIM: To probe into the genetic susceptibility of HLA-DRB1 alleles to esophageal neoplasm in Hubei Han Chinese. METHODS: HLA-DRB1 gene polymorphism in 42 patients with esophageal neoplasm and 136 normal control subjects was studied by PCR and sequence. RESULTS: Allele frequency of HLA-DRB1 *0901 allele was significantly higher in esophageal cancer patients than those in normal controls(0.2500 vs 0.1397, P =0.028; the odds ratiO².053; etiologic fraction 0.1282).There were no association between the rested HLA-DRB1 alleles with patients. CONCLUSION: Individuals carrying HLA-DRB1 *0901 may be susceptible to esophagealo carcinoma, its nucleotide sepuence approachs to the corresponded allele sequence(exoN²)published in GenBank.