探讨园林绿化的市场运作

将园林绿化的工作通过市场的运作,逐步实现市场管理,从无形到有形,从无序到有序的转变。     

南方双季稻区小行距插秧机的改进设计与试验

针对300mm行距插秧机在南方双季稻区栽插行距过大、穴数过少及不能充分发挥机插稻的增产潜力问题,在300mm行距插秧机结构的基础上,通过机械优化设计和田间农艺技术相结合的方法,对其插植部箱体、苗箱、支架(包括左右支架和中间支架)和浮板4个关键部位技术参数改进设计,研制出了适合南方双季稻区作业的2ZS-488B型(264mm行距)插秧机,并于2012-2013年在江西省2个试验点进行不同早晚稻品种机插行距的大田对比试验。结果表明:该插秧机作业性能稳定,漂秧率、伤秧率和漏插率分别为1.55%、2.68%和1.93%,相对均匀度合格率为89.54%。与300mm行距插秧机相比,其产量平均增产529.43kg/hm2,平均增产率达8.57%。该研究结果创新了南方双季稻区新的机械化栽插方式,有利于农机农艺的有效融合。     

通过转化脂肪酸去饱和酶基因AcoFAD2提高菠萝植株的抗寒能力

为培育抗寒菠萝新品种,本研究通过比较菠萝脂肪酸去饱和酶基因序列和拟南芥脂肪酸去饱和酶基因序列,筛选获得目标基因AcoFAD2;通过农杆菌转化菠萝'台农17'获得过表达AcoFAD2转基因植株TN17FAD2-3;转基因植株和对照在低温条件下进行培养,鉴定转基因植株和对照的不饱和脂肪酸含量及抗寒能力.结果 发现组培苗在7℃条件下处理5d然后转入26℃生长一周,TN17FAD2-3第四片叶坏死比例为(5±1)％,只转化空载体的对照TN17-EV第四片叶坏死比例为(97±2)％.组培苗在7℃条件下生长5d,然后转入26℃生长15d.TN17FAD2-3第二片叶叶面积为(2.15±0.2) cm2,TN17-EV第二片叶叶面积为(0.06±0.01) cm2.TN17FAD2-3的叶片不饱和脂肪酸含量(16∶3+18∶3)为(77.5±0.7)％,对照TN17-EV叶片不饱和脂肪酸(16∶3+18∶3)含量为(58.6±0.8)％.TN17FAD2-3的叶片不饱和脂肪酸含量高于只转化空载体的对照TN17-EV.低温条件下,TN17FAD2-3比TN17-EV生长快,TN17FAD2-3株系比TN17-EV具有更高的抗寒性,载体UBI-pCAMBIA1301不能提高菠萝植株的抗寒能力,通过转化脂肪酸去饱和酶基因AcoFAD2能够提高菠萝植株的抗寒性能,本研究为快速培育抗寒菠萝新品种提供理论基础.     

黄土丘陵区不同管理方式下草地优势种群的生态位

以吴起县杨青川流域草地为研究对象,对封育(Enclosure)、放牧(Grazing)、施肥(Fertilization)、刈割(Clipping)、灭鼠(Deratization)5种管理方式的草地群落进行调查,并运用Levins生态位宽度和Pianka生态位重叠指数对5种管理方式下主要植物种群生态位特征进行分析。结果表明,达乌里胡枝子(Lespedeza davurica)、铁杆蒿(Artemisia sacrorum)、赖草(Leymus secalinus)、猪毛蒿(Artemisia scoparia)和硬质早熟禾(Poa sphondylodes)的种群总生态位宽度较大,封育放牧施肥刈割灭鼠管理模式下,生态位宽度最大的分别是达乌里胡枝子、赖草、紫花地丁(Viola philippica)、达乌里胡枝子和猪毛蒿,生态位宽度值大于4的物种数分别为6、6、3、4和3种。不同管理方式下各种对间的重叠指数平均值由大到小依次封育放牧施肥刈割灭鼠。施肥管理中,种群间生态位宽度与生态位重叠之间存在线性关系,其它管理方式中种群生态位宽度与生态位重叠之间不存在线性关系。生态位分析表明,封育和放牧管理下种群间对资源的需求趋于相同,彼此间通过竞争共存,有利于群落演替,草地生态系统逐渐得到恢复,施肥、刈割、灭鼠管理使群落物种竞争排序发生变化,破坏了草地生态系统原有的竞争机制,导致群落向简单群落演替。从牧草发展角度出发,封育、施肥和刈割有利于优质牧草生长。     

试述北京市农机报废更新工作的迫切性

为保证北京市农机安全生产工作,大力促进农业生产的发展,北京市建立农机报废更新制度迫在眉睫。     

Analysis of Inter-Individual Bacterial Variation in Gut of Cicada Meimuna mongolica (Hemiptera: Cicadidae)

Intestinal bacterial community plays a crucial role in the nutrition, development, survival, and reproduction of insects. When compared with other insects with piercing-sucking mouthparts, the habitats of cicada nymphs and adults are totally different. However, little is known about the differences in the gut bacterial communities in the nymphs and adults within any cicada species. The diversity of bacteria in the gut of nymphs and adults of both genders of Meimuna mongolica (Distant) was studied using the denaturing gradient gel electrophoresis (DGGE) method. Few inter-individual variations among gut microbiota were observed, suggesting that M. mongolica typically harbors a limited and consistent suite of bacterial species. Bacteria in the genera Pseudomonas and Enterobacter were the predominant components of the gut microflora of M. mongolica at all life stages. Bacteria of Pantoea, Streptococcus, and Uruburuella were also widespread in the cicada samples but at relatively lower concentrations. The relative stability and similarity of the PCR-DGGE patterns indicate that all individuals of this cicada species harbor a characteristic bacterial community which is independent from developmental stages and genders. Related endosymbionts that could be harbored in bacteromes of cicadas were not detected in any gut samples, which could be related to the cicada species and the distribution of these endosymbionts in the cicada cavity, or due to some of the possible limitations of PCR-DGGE community profiling. It is worthwhile to further address if related cicada endosymbiont clades distribute in the alimentary canals and other internal organs through diagnostic PCR using group-specific primer sets.     

Evaluation of the colonization capabilities of Salmonella Enteritidis in Quails using an RT-PCR approach

We used a real-time PCR assay and indirect fluorescent antibody (IFA) assay to detect genomic DNA of Salmonella Enteritidis in the internal organs of quails after an oral challenge. The results showed that S. Enteritidis was detected in all the samples at different time points. This study will assist a future understanding of the pathogenesis of S. Enteritidis.