Leaf carbohydrates assimilation and metabolism affect seed yield of rapeseed with different waterlogging tolerance under the interactive effects of nitrogen and waterlogging

Waterlogging is a main factor causing rapeseed (Brassica napus L.) yield loss, and reasonable nitrogen (N) applications can compensate for this loss. To investigate the effects of N rates on seed yield of waterlogged rapeseed, the waterlogging-tolerant rapeseed variety ZS 9 and sensitive variety GH01 were waterlogged for 0 and 10 days with five leaves at the seedling stage under four N rates (0, 90, 180 and 270 kg/ha). Waterlogging significantly decreased seed yield, while N application can alleviate the yield loss. The yield decrease rate of waterlogged GH01 was greater than that of ZS 9 under the same N rate. During the seedling and bolting stage, the leaf photosynthetic rate (Pn) and ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) activity increased, while activities of adenosine diphosphate glucose pyrophosphorylase (AGPase), sucrose synthase (SuSy) and sucrose phosphate synthase (SPS) decreased with more N under the same watering conditions. Compared to the plants without waterlogging, the leaf Pn and Rubisco activity, starch and sucrose contents of waterlogged rapeseed decreased at the two stages; activities of AGPase, SuSy and SPS of waterlogged rapeseed decreased at the seedling while increased at the bolting stage for both the two varieties. At the flowering stage, the Pn, the activities of Rubisco, AGPase, SuSy, SPS and contents of sucrose, starch increased with more N application for both ZS 9 and GH01. Compared to the plants without waterlogging, the Pn and Rubisco activity for waterlogged plants of the two varieties increased; the waterlogged plants of tolerant variety had higher activities of AGPase, SuSy and SPS, while those of sensitive variety was significantly lower. However, the decreased starch and sucrose content were found in both tolerant and sensitive varieties. The activities of AGPase, SuSy and SPS at flowering were highly positively correlated with yield under the interactive effects of N and waterlogging. These results suggested that the flowering stage is the most important stage that N had the positive regulation on waterlogged rapeseed growth. The carbohydrates translocation from leaves to seeds of the tolerant variety were enhanced after waterlogging, while that of the sensitive variety was still inhibited. This was the main reason for the difference in yield between the two waterlogged varieties.     

花生壳黄酮的提取纯化工艺

本文采用酶法预处理结合超声波辅助提取的方式，最大程度地提高了花生壳总黄酮的得率，并优化大孔树脂纯化工艺，提高了有效成分的纯度。花生壳黄酮的最佳提取工艺为：花生壳粉与水混合，半纤维素酶与木聚糖酶按1:1（m/m）复配，用量0.25‰，50℃酶解30 min后，按料液比1:20（m/V）加入乙醇至终浓度60%，于功率1000 W，55℃超声波辅助提取60 min，花生壳总黄酮的得率约为2.5%。选用D101型大孔树脂，上样缓冲液为pH 5.0的60%乙醇溶液，洗脱液为pH 10.0的70% 乙醇溶液，上样与洗脱流速为0.75 BV/h和1.5 BV/h。纯化后的花生壳总黄酮和木犀草素的纯度分别为10.54%和5.85%，提高了90%和120%。     

优质国审棉品种——ZHM19

概述了ZHM19的选育过程、特征特性、产量、纤维品质和抗病性等特点及主要栽培技术措施。     

Screening of antagonistic Trichoderma strains and their application for controlling stalk rot in maize

Maize is one of the major crops in China, but maize stalk rot occurs nationwide and has become one of the major challenges in maize production in China. In order to find an environment-friendly and feasible technology to control this disease, a Trichoderma-based biocontrol agent was selected. Forty-eight strains with various inhibition activities to Fusarium graminearum, and Fusarium verticillioides were tested. A group of Trichoderma strains(DLY31, SG3403, DLY1303 and GDFS1009) were found to provide an inhibition rate to pathogen growth in vitro of over 70%. These strains also prevented pathogen infection over 65% and promoted the maize seedling growth for the main root in vivo by over 50%. Due to its advantage in antifungal activity against pathogens and promotion activity to maize, Trichoderma asperellum GDSF1009 was selected as the most promising strain of the biocontrol agent in the Trichoderma spectrum. Pot experiments showed that the Trichoderma agent at 2–3 g/pot could achieve the best control of seedling stalk rot and promotion of maize seedling growth. In the field experiments, 8–10 g/hole was able to achieve over 65% control to stalk rot, and yield increased by 2–11%. In the case of natural morbidity, the control efficiency ranged from 27.23 to 48.84%, and the rate of yield increase reached 11.70%, with a dosage of Trichoderma granules at 75 kg ha~(-1). Based on these results, we concluded that the Trichoderma agent is a promising biocontrol approach to stalk rot in maize.     

不同新型作用机制杀菌剂对梨树主要病菌毒力及防治流程应用

 为明确多种新型作用机制杀菌剂与引起梨树褐斑病、黑星病、白粉病等病原菌的有效对靶关系及制定梨树主要病害防治流程,采用菌丝生长速率法、离体叶片法与田间药效方法研究新型杀菌剂对靶标病原菌的毒力、对靶标病害的防效及其田间有效应用,建立替代梨树主要病害传统化学杀菌剂的防治流程技术。结果显示,双胍三辛烷基苯磺酸盐在离体叶片法下对褐斑病的防效大于85%,田间药效验证3次用药后7 d防效大于85%、30 d防效大于80%、90 d防效仍大于60%,兼治轮纹病菌其毒力EC₅₀值均小于1 μg·mL^-1。双胍三辛烷基苯磺酸盐、辛菌胺醋酸盐、吩嗪α-2羧酸在离体叶片法下对黑星病防效大于90%且毒力EC₅₀值小于1 μg·mL^-1;田间药效验证1次用药后7 d防效大于80%、30 d防效仍大于75%。噻肟菌酯、硝苯菌酯、丙硫菌唑在离体叶片法下对白粉病的防效大于85%;田间药效验证3次用药后7 d铲除效果大于70%、30 d仍大于60%。丙硫菌唑对黑斑、轮纹病菌毒力EC₅₀值均小于1 μg·mL^-1;吩嗪α-2羧酸同时对褐斑、黑斑、轮纹病菌毒力EC₅₀值小于1 μg·mL^-1。针对梨树主要病害发生期,选用新型杀菌剂替代传统杀菌剂制定防治技术流程,其综合防效达到88.94%。不同新型作用机制杀菌剂在防治梨树主要病害上的应用,能够降低抗药性产生,同时达到有效防治的目的。     

基于茎秆生物力学特性的油菜抗倒调控机制研究

为了应用生物力学特性指标对茎秆抗倒性进行评价，进而指导油菜抗倒栽培，以华杂62和金油杂158为试验材料，基于不同栽培因素下油菜茎秆的弹性模量、弯曲强度、剪切强度及抗倒性，分析了栽培因素对油菜茎秆力学特性指标的影响及其与抗倒性的相关性。结果表明：油菜抗倒性与茎秆的弹性模量、弯曲强度、剪切强度呈显著负相关；随着播期推迟，油菜茎秆的弹性模量、弯曲强度及剪切强度分别减小15.31%、29.16%和13.88%，倒伏指数增大32.18%；随着播种密度增大，油菜茎秆的弹性模量、弯曲强度及剪切强度均呈先增大后减小趋势，而倒伏指数先减小后增大；随着施氮量增加，油菜茎秆的弹性模量、弯曲强度及剪切强度均逐渐减小，而倒伏指数逐渐增大，与施氮量120 kg·hm^-2处理相比，在施氮量为360 kg·hm^-2下，油菜茎秆的弹性模量、弯曲强度及剪切强度分别减小39.43%、19.40%和16.63%，倒伏指数增大16.36%。因此，播期提前、适当增加播种密度、控制氮肥投入，有助于提高油菜茎秆的力学特性强度，从而增强油菜的抗倒伏能力。研究结果可为油菜抗倒栽培调控提供理论依据。     

广西田园综合体的建设现状和发展建议

文章通过对田园综合体的概念进行介绍，找出广西田园综合体发展情况和存在的问题，最后 提出解决广西田园综合体存在问题的对策和建议，从而促进广西农业的快速发展，带动当地经济稳步 提升。     

我国农业机械的推广与对策研究

新时期下，由于我国宣传推广的力度不够、当地基层群众综合素养不高、机械使用不当等原 因并没有形成使用农业机械进行耕作的习惯，在我国西南部、东南部等丘陵地带，仍然采用牛拉车等 较为落后的耕作方式，从而导致农业机械化带来的提高种植效率，本文目重点就我国的农业机械推广 存在的问题进行概述，并提出相关对策。     

陇东旱塬区复种不同藜麦品种(系)的适应性初步评价

为分析不同藜麦品种(系)在陇东雨养地区夏播复种的生态适应性,以12个藜麦品种(系)为材料,对其物候期、农艺性状、经济性状、品质性状等指标进行考察,采用相关性分析、主成分分析和聚类分析法对其适应性进行综合评价。结果表明:供试的12个藜麦品种(系)除LY-2无法复种成熟外,其余的11个品种(系)均能完成生育期;对其19个性状进行相关性分析表明,单位面积籽粒产量与单株粒质量和千粒质量呈极显著正相关(P0.01),而与根倒率、茎倒率呈极显著负相关(P0.01);株高与千粒质量呈极显著正相关(P0.01),籽粒粗蛋白和淀粉分别与籽粒直径和千粒质量呈极显著正相关(P0.01);对其15个性状指标进行主成分分析和聚类分析,对提出的5个主成分累计贡献率达85.04%,根据综合得分,筛选出适应性最好、得分最高的2个品种(系)‘陇藜4号’和‘Q2’;聚类分析表明,11个藜麦品种(系)系统聚为3大类型,各品种(系)间性状与遗传距离方面存在较大差异,其中第三类产量最高,第二类有矮秆、早熟等特性,可根据生产需要和育种目标进行综合考虑。     

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.