砂藓(Racomitrium canescens)抗旱相关基因RcAOS2的克隆及表达分析

丙二烯氧化物合酶(allene oxide synthase, AOS)是茉莉酸合成途径中关键酶,在茉莉酸合成中具有重要的作用。本研究在砂藓(Racomitrium canescens)干旱胁迫转录组数据中发现一个干旱胁迫下表达量上调的AOS基因,将其命名为RcAOS2,我们对RcAOS2的开放阅读框进行了克隆及相关的生物信息学预测分析,并对RcAOS2在砂藓快速脱水和复水过程中的表达量变化进行了检测。结果显示,该基因cDNA全长1 474 bp,开放阅读框长516 bp。RcAOS2编码蛋白质的相对分子质量为4.36 kD,等电点为5.11,不稳定系数为55.02,为不稳定蛋白质;脂肪系数为19.19;RcAOS2蛋白质疏水性较强,属于疏水性蛋白质,存在信号肽,不属于跨膜蛋白质。系统进化分析表明,RcAOS2蛋白质与其他物种AOS蛋白质亲缘关系较远,是具有AOS序列特征的新类型。实时荧光定量PCR分析结果表明RcAOS2基因在砂藓干旱和复水过程中呈现差异性表达,推测RcAOS2可能参与砂藓的干旱胁迫响应和复水回复过程。本研究成果为进一步研究砂藓抗旱基因功能提供理论基础和备选基因资源。     

不同基质活性炭对阿特拉津吸附特性研究

为了解决阿特拉津给土壤带来的污染问题以及寻找吸附效果较好的活性炭基质,本研究利用高效液相色谱(HPLC)技术检测了阿特拉津溶液和悬浮液经煤、木、果和竹质4种生物炭处理后的残留量,并对其在阿特拉津溶液和土壤中的吸附动态进行检测。结果表明,煤质活性炭对初始浓度为100 mg/L和10 mg/L的阿特拉津溶液和悬浮液的吸附效果较好,其吸附率为5.651%~68.42%;当阿特拉津初始浓度为100 mg/L时,煤质活性炭在40 min时对阿特拉津溶液的吸附率高达23.49%;与对照组相比,当阿特拉津的初始浓度为100 mg/L时,土壤中阿特拉津经煤质活性炭处理42天后的残留浓度最低,活性炭吸附率达到91.39%。综上,煤质活性炭能有效降解溶液及土壤中阿特拉津含量,这将为阿特拉津污染土壤的改良研究奠定基础。     

湖南省粮食产量波动的影响因素分析及预测

旨在维护国家稳定,为预判粮食生产前景、提高粮食生产效率、保障粮食安全提供理论依据。利用湖南省统计数据,运用灰色关联分析法筛选关联性较强的影响因素,并建立GM(1,N)预测模型预测粮食产量。2008—2017年与湖南省粮食产量关联度最大的影响因素是粮食作物播种面积和农业机械总动力;科技因素是影响2008—2017年湖南省粮食产量的主要因素,其次是自然因素,社会因素;2018—2027年湖南省粮食产量有较小波动,且农业机械总动力和财政农业支出影响较大;农业机械总动力在前后十年对粮食产量都有较重要的影响,越来越占据主导地位。粮食产量受国家政策的影响,受农业机械总动力影响最大,维持产量水平需高度重视农业机械化水平,稳步提高粮食作物播种面积。     

农业生产基地项目环境影响评价要点分析及探讨

农业生产基地项目具有影响范围大、产品服务多元化等特点，涉及行业类别较多，其环境影响评价文件也相对复杂。环境影响评价报告编制单位应充分与建设方进行沟通，熟悉项目建设内容，挖掘项目可能的产生污染的环节和设施，明确环境影响范围和环境敏感点，并对项目损益进行两方面的分析。     

两型社会建设背景下生态效率评价研究——以湖南省为例

基于"两型"社会建设的目标与内涵,选取了湖南省生态效率综合评价指标,以2003—2012年湖南省数据为样本,采用DEA数据包络分析法计算各年份的生态效率,并对不同年份的能源消耗量、水资源消费量以及三废的排放量进行深入分析。结果表明,随着湖南省GDP的增长,生态效率也不断在提高。针对不同的资源产出率和环境产出率,湖南省应树立可持续发展理念,实现经济由粗放型发展向集约型发展转变;发展创新技术,推进湖南省两型社会的发展;完善法律法规体系,加大宣传力度,改变保守观念,提高人们的环保意识。     

气相色谱-串联质谱法测定柑橘中5种杀螨剂残留

建立了气相色谱-串联质谱法(GC-MS/MS)检测柑橘中5种杀螨剂残留分析方法。样品经乙腈提取、氯化钠盐析后,取有机相用Qu EChERS方法净化,利用GC-MS/MS在多反应监测(MRM)模式下进行测定,外标法定量。5种杀螨剂在0.005~0.5mg/L浓度范围内呈现良好的线性关系,相关系数r^2均>0.996,方法定量限为0.005 mg/kg。在0.005、0.01和0.1mg/kg 3种添加水平下,加标回收率为70.6%~111.3%,相对标准偏差(RSD)为1.07%~14.64%。本方法简便、重现性良好,可用于柑橘类水果样品中杀螨剂的日常检测。     

Identification and expression analysis of 11 MADS-box genes in peach (Prunus persica var. nectarina ‘Luxing’)

MADS-box genes play a central role in the development of flowers in plants. In this study, 11 PpMADSs were isolated from ‘Luxing’ peach, and the expression levels were detected in different tissues and fruit development. Eleven PpMADSs, designated as PpMADS13, 14, 18, 23, 24, 25, 32, 33, 34, 35, and 39 were isolated. Phylogenetic analysis revealed that PpMADS13, 14, and 18 belonged to SVP, AGL15, and MIKC* group respectively; PpMADS23, 24, 25, and 39 were in the Mα group; PpMADS32, 33, 34, and 35 belonged to the Mγ group. Predictions from subcellular localization showed that 10 PpMADS were located in the nucleus. RT-PCR revealed that PpMADS13 was expressed in stems, leaves, and during fruit development (70d); PpMADS14 was expressed in sepals, stamens, petals, and during flower development; PpMADS18 was expressed in roots, stems, leaves, sepals, ovaries, stamens, petals, and during flower and fruit development; all MADS-box genes (expect for PpMADS33) in the Mα and Mγ group were expressed in roots, stems, leaves, sepals, ovaries, stamens, petals, and during flower development; few genes were expressed during fruit development. These results indicated that PpMADS may play a crucial regulatory role in vegetative growth and development processes of flowers and fruits in peaches.     

Pathogen Analysis of Goat's Respiratory Diseases

To investigate the pathogens of goat's respiratory disease from a goat farm in Guangxi province, the epidemiological investigation, clinic observation, pathological examination, bacterium isolation and identification, biochemical test, PCR and animal experiment test were conducted.The preventive and control measures were taken on the basis of pathogen epidemiological characteristics and drug sensitive test results.The results showed that Mycoplasma, influenza virus and parasite were negative by isolation and culture or PCR, however, two strains of gram-negative bacteria named MS1 and MS2 were isolated from lung.MS1 was identified as Serratia marcescens by biochemical test and 16S rRNA sequencing, which shared 99% nucleotide homology with other Serratia marcescens in GenBank.And MS2 was identified as E.coil by the same methods that shared 99% nucleotide homology with other E.coli in GenBank.Animal experiment showed that two strains could cause death in mice.The drug sensitive tests showed two strains were highly sensitive to spectinomycin, amikacin, kanamicin and neomycin.Kanamycin and dexamethasone were used to treat the sick goats, and achieved good results.     

质量控制图在水产饲料氨基酸分析中的应用

通过对实验室自制标准物料-豆粕样品中氨基酸含量的多次测定,建立X-S质量控制图,开展水产饲料氨基酸分析日常质量控制。试验按照GB/T 18246-2000,通过微波水解-离子交换-柱后衍生-紫外检测法对豆粕样品氨基酸含量进行连续测定,并以FAPAS奶粉标准物质验证,利用偏度-峰度检验法对离群值进行判断,建立赖氨酸、甘氨酸、氨基酸总量质量控制图。结果显示,质量控制图中豆粕质控样赖氨酸、甘氨酸、氨基酸总量测定的RSD值均小于4%,FAPAS奶粉标准物质测定值落在参考范围内,建立的质量控制图能对日常氨基酸检测结果进行有效监控。结果表明,所建立氨基酸质量控制图直观有效,能对过程存在的异常因素起到预警作用,并可节约成本。