秸秆还田与优化施氮改善烤烟根际土壤碳氮转化及氮素吸收

针对华南沙泥田烟区氮肥过量施用导致烟叶品质下降的问题,拟通过秸秆还田与氮肥优化配施调节烤烟各生育期氮吸收、根际土壤碳氮转化及相关酶的活性。试验采用随机区组设计,设水稻秸秆还田与氮肥两因素,其中3个碳（秸秆还田）水平：C0,无秸秆还田,0 kg/hm ²;C1,中量秸秆还田,4500 kg/hm ²;C2,全部秸秆还田,9000 kg/hm ²;2个氮水平：N1,传统施氮,169.50 kg/hm ²;N2,优化施氮,105.00 kg/hm ²。结果表明,与N1相比,N2处理秸秆还田下烤烟前期烟叶和根系氮吸收和累积正常,而后期有所下降;C1、C2处理时,与现蕾期相比,成熟期时根系氮含量均降低4.2 g/kg,叶片氮含量降低3.8、3.0 g/kg;成熟期时,与N1处理相比,N2处理时C1、C2处理的土壤无机氮含量降低30.4%、20.0%,前期2个氮处理间土壤无机氮含量无差异,优化施氮下中量秸秆还田（C1N2）处理烤烟土壤NH₄ ⁺-N含量在整个生育期内较高且呈降低趋势,而硝态氮和土壤无机氮含量在成熟期最低,表明中量秸秆还田下优化施氮能够维持生育前期土壤无机氮含量,且降低成熟期土壤无机氮含量。2个秸秆还田量处理时,团棵期N2处理的土壤转化酶活性是N1处理的1.30、1.13倍;旺长期土壤转化酶活性是N1处理的1.27、1.10倍;与传统施氮相比,秸秆还田下优化施氮处理增加了整个生育期土壤脲酶、磷酸酶、过氧化氢酶活性。在中量秸秆还田（C1）处理下,与N1水平相比,现蕾期和成熟期的N2处理土壤水溶性碳含量提高11.2%和14.1%;与N1相比,N2处理的土壤微生物量氮含量呈降低趋势。综上所述,优化施氮耦合中量秸秆还田（C1N2）能够提高土壤水溶性碳含量,维持土壤氮素合理供应,稳定烤烟生育前期对氮素吸收与累积,减少生育后期烟叶氮素奢侈吸收,与烤烟吸氮规律比较吻合。     

基于RNMU的多源星载SAR影像融合与土地覆盖分类

为充分利用多时相、多极化SAR数据在不同土地覆盖类型中的后向散射特性,将递归非负矩阵下近似(Recursive nonnegative matrix underapproximation,RNMU)算法引入多源SAR数据的融合,并利用融合后的SAR影像实现较高精度的土地覆盖分类。融合过程中,在根据不同模式SAR影像特点进行多源SAR影像预处理的基础上,基于RNMU算法通过对多个输入SAR影像进行矩阵分解及迭代最优矩阵求解,得到融合影像。为验证融合后SAR影像在土地覆盖分类中的应用效果,以吉林省大安市为研究区,对多时相Sentinel-1的VV/VH双极化SAR数据和高分三号(GF-3)的HH/HV双极化SAR数据进行了基于RNMU的影像融合,并利用融合后的SAR影像进行研究区主要土地覆盖类型分类。实验结果表明,基于RNMU融合影像的土地覆盖分类总体精度达93. 11%,Kappa系数为0. 86,与Gram-Schmid(G-S)融合方法相比,分类总体精度提高了6. 83个百分点,Kappa系数提高0. 12。多源SAR融合为SAR影像融合提供了有效手段,为土地覆盖分类提供了更多高精度的数据资源。     

ROCK promotes high glucose-induced cardiomyocyte apoptosis by inhi-biting PI3K/Akt signaling pathway

AIMTo investigate whether Rho-associated coiled-coil kinase (ROCK) is involved in high glucose-induced apoptosis of primary cardiomyocytes by regulating PI3K/Akt signaling pathway. METHODSPrimary Wistar rat cardiomyocytes were cultured and identified by α-sarcomeric actin (α-SCA) immunohistochemistry. Cardiomyocytes were treated with 5.5, 33 and 40 mmol/L glucose for 48 h. The cell viability was measured by MTT assay, and the mRNA expression of ROCK1 and ROCK2 in the cardiomyocytes was detected by RT-qPCR. Flow cytometry was used to analyze the apoptosis of the cardiomyocytes. The protein levels of ROCK1, ROCK2, cleaved caspase-3, Bcl-2, PI3K, Akt and p-Akt were determined by Western blot. In order to confirm the regulatory effect of ROCKs on PI3K/Akt signaling pathway, the cells were divided into control group (5.5 mmol/L glucose), high glucose group (33 mmol/L glucose) and high glucose+Y27632 (ROCK inhibitor) group. Western blot was used to detect the protein levels of ROCK1, ROCK2, PI3K, Akt and p-Akt. RESULTSAfter 48 h of high glucose exposure, the values of relative cell viability in 33 and 40 mmol/L glucose groups were (79.71±2.43)% and (68.41±7.49)%, respectively, both of which were significantly decreased compared with normal control group (P<0.05). After 48 h of high glucose exposure, the relative mRNA levels of ROCK1 and ROCK2 in 33 and 40 mmol/L glucose groups were significantly increased compared with normal control group (P<0.05). Compared with normal control group, the apoptotic rate in 33 and 40 mmol/L glucose groups was increased significantly (P<0.05). Compared with normal control group, the protein expression of ROCK1, ROCK2 and cleaved caspase-3 in 33 and 40 mmol/L glucose groups was increased (P<0.05), while the protein expression of Bcl-2 was decreased (P<0.05). No significant difference in the protein levels of PI3K and Akt among the 3 groups was observed, while the protein level of p-Akt in 33 and 40 mmol/L glucose groups was decreased compared with normal control group (P<0.05). Compared with high glucose group, the expression of ROCK1 and ROCK2 was decreased in high glucose+Y27632 group. No significant difference in the protein levels of PI3K and Akt among the 3 groups was observed. Compared with normal control group, the protein level of p-Akt in high glucose group was decreased, and the protein level of p-Akt in high glucose+Y27632 group was increased significantly compared with high glucose group. CONCLUSION Under high glucose environment, ROCK may reduce the level of p-Akt by inhibiting the PI3K/Akt signaling pathway， thus promoting the apoptosis of cardiomyocytes.     

四川地区猕猴桃病毒1的RT-PCR检测及外壳蛋白基因序列分析

为了明确近期新西兰报道的侵染猕猴桃的新病毒——猕猴桃病毒1（Actinidia virus 1，AcV-1）在四川地区猕猴桃上的发生情况及其分子特性，采用RT-PCR对来自四川6个地区疑似感染病毒的90份猕猴桃主栽品种‘红阳’和‘金果’的叶片样品进行检测。结果表明，22份样品为AcV-1阳性，检出率为24.4%。将获得的5个AcV-1分离物和已报道的新西兰分离物K75的外壳蛋白（coat protein，CP）基因序列进行比对，结果表明，分离物间核苷酸序列和氨基酸序列的相似性分别为84.8% ~ 97.1%和89.7% ~ 99.6%，其中除邛崃分离物HYH5与新西兰分离物K75的核苷酸序列相似性较高（97.1%）外，其余4个分离物均低于91%。系统进化分析结果显示，这些分离物主要聚集在3个分支上，分离物HYH5与新西兰分离物K75位于同一分支，其余分离物位于另外2个分支。     

芜菁Br14-3-3的克隆及其在非生物胁迫下的表达分析

克隆了‘津田芜菁’（Brassica rapa subsp. rapifera‘Tsuda’）通用调节因子14-3-3基因cDNA序列，命名为Br14-3-3（GenBank登录号为MK896872）。该基因全长1 113 bp，开放阅读框全长774 bp，编码含有257个氨基酸的多肽。荧光定量PCR分析Br14-3-3在‘津田芜菁’不同组织中及其在温度、脱水、渗透、ABA和无机盐等非生物胁迫下幼苗中的表达，结果表明该基因在‘津田芜菁’的花中表达量最高，幼苗中次之；低温抑制了Br14-3-3的表达，其他非生物胁迫可诱导该基因表达，暗示Br14-3-3在非生物胁迫应答中发挥功能。     

番茄斑萎病毒病抗性种质筛选及人工接种鉴定方法优化

对154份番茄材料(包括普通番茄76份,樱桃番茄78份)进行两年两次田间番茄斑萎病毒病的病情指数调查,筛选出14份对番茄斑萎病毒病具有稳定抗性的番茄材料,利用sw-5-2共显性SCAR标记对田间表现抗病的材料进行分子标记鉴定,发现3份抗病材料携带抗番茄斑萎病毒病的Sw-5基因。为缩短番茄斑萎病毒病人工接种鉴定周期,以含有sw-5的抗病材料H8和感病材料M82为研究对象,设置4、6、8、10片真叶4个接种时期,分别在接种后14、21、28 d进行病情指数调查和抗性分级,结果表明,6片真叶期接种,接种后28 d进行病情调查即可有效鉴别植株番茄斑萎病毒病抗性,与8、10片真叶期接种效果相同,人工接种抗病性鉴定效率显著提升。     

胡葱黄条病毒吉林毛葱分离物全基因组序列测定与分析

使用RT-PCR方法从吉林省疑似感染胡葱黄条病毒(Shallot yellow stripe virus,SYSV)的分蘖洋葱(毛葱)叶片中获得了SYSV吉林毛葱分离物SYSV-JL(MN607702)的全基因组序列。SYSV-JL的全长序列为10?427 nt,与GenBank已登录的3条SYSV全长或近全长序列在多个基因上保持着较高的序列一致性,但在P1基因上核苷酸和氨基酸序列一致性较低,分别为69.5%～84.2%和60.9%～76.9%,进一步通过变异分析发现,P1基因包含369个变异位点,表现出较为明显的高变异特征。系统发育分析显示,不同SYSV分离物具有较为明显的地区差异,SYSV-JL分离物与多个中国分离物系统发育关系较近。     

虎雪兰玻璃化超低温法脱毒技术的研究

以兰属花卉虎雪兰组培原球茎为试材,采用玻璃化超低温法对兰花病毒脱除进行了研究,以期为虎雪兰玻璃化超低温法脱毒体系的建立提供参考依据。结果表明:在蔗糖浓度0.5 mol·L-1预培养4 d,然后在蔗糖0.6 mol·L-1加载液冰上处理50 min,之后转入PVS2溶液冰上玻璃化处理120 min,再液氮冷冻40 min,37℃水浴解冻3 min,最后卸载液(1/2MS+1.2 mol·L-1蔗糖)卸载20 min,待恢复培养后,原球茎成活率可达到65%以上,随机检测不同处理样品的脱毒率可达97%。     

赤霉素不同处理浓度和浸种时间对托鲁巴姆发芽的影响

托鲁巴姆种子的休眠较深,发芽较困难。为了打破其种子的休眠期,加快种子萌发,提高种子发芽的整齐度,以托鲁巴姆为试材,研究了不同的赤霉素处理浓度和浸种时间对其发芽的影响。结果表明:生产中适宜的赤霉素处理浓度为750~1 250 mg/L,浸种时间为36 h,发芽率可达93.00%;可有效提高托鲁巴姆种子的发芽速率和发芽整齐度。     

Temperature modulates liver lipid accumulation in Atlantic salmon (Salmo salar L.) fed low dietary levels of long‐chain n‐3 fatty acids

Atlantic salmon (Salmo salar) were fed five graded levels of eicosapentaenoic acid (EPA, 20:5n‐3) and docosahexaenoic acid (DHA, 22:6n‐3), from 1.4 to 5.2% of total fatty acids (FA, 5–17 mg kg^?1 feed), and grew from ~160 g to ~3000 g, with the period from 1450 g onwards conducted both at 6 °C and at 12 °C. All fish appeared healthy, and there were no diet‐related differences in haematological or plasma parameters, as well as intestinal histological or gut microbiota analysis. Fish reared at 6 °C had higher accumulation of storage lipids in the liver compared to fish reared at 12 °C. Liver lipids also increased with decreasing dietary EPA + DHA at 6 °C, while there was no such relationship at 12 °C. Gene expression of SREBP1 and 2, LXR, FAS and CPT1 could not explain the differences in liver lipid accumulation. In liver polar lipids, DHA was found to be reduced when dietary EPA + DHA was <2.7% of FAs, while the level of EPA in the membranes was not affected. In conclusion, reducing dietary EPA + DHA from 5.2 to 1.4% of total FAs had a minor impact on fish health. Temperature was the factor that most affected the liver lipid accumulation, but there was also an interaction with dietary components.