薄型高密度纤维板生产设备的要求分析

对薄型中高密度纤维板生产设备的要求作了简要分析。

Abstract：

A brief analysis is made of the requirements for thin medium high density fiberboard product manufacturing equipment.     

南瓜银叶突变体48a的表型特征及其遗传学分析

南瓜银叶突变体48a是在嫩食型中国南瓜中分离筛选到的稳定遗传自交系,银色叶不仅可以作为标记性状应用到育种中,还可为南瓜抗虫、抗病、耐寒等一系列研究提供重要的材料基础。笔者对银叶突变体的表型特征及叶片的解剖结构进行鉴定分析,发现植株整体长势、熟性与野生型无明显差异;成熟叶片正面全部呈银灰色,叶绿素含量明显降低,叶片上表皮细胞与栅栏细胞间明显剥离,存在明显的空隙。利用突变体48a和野生型49a南瓜自交系构建的六世代遗传群体,调查发现F2的绿叶与银叶符合3∶1的分离比,回交群体BC1P1分离比符合1∶1,表明南瓜银色叶性状由单隐性基因控制。     

快速灵敏的甘蔗线条花叶病毒免疫学检测体系的建立

 甘蔗花叶病广泛存在于我国甘蔗种植区,严重影响甘蔗产业的高质量发展。近年来甘蔗线条花叶病毒在蔗区肆虐,尽管针对其的血清学检测技术已经建立,但是快速、准确、高通量的检测方法亟待发掘。本研究制备了^SCSMVCP的抗血清,特异性高,与引起甘蔗花叶病的另两种病原 (高粱花叶病毒和甘蔗花叶病毒) 间没有血清学交叉反应。基于该多克隆抗体,建立了直接抗原包被的ELISA、斑点杂交、Western blot和基于多抗的免疫试纸条检测技术。开发的免疫试纸条检测技术能快速、准确、高通量应用于田间病毒鉴定。本文提供了基于血清学的快速、准确、高通量,且便捷的甘蔗线条花叶病毒检测技术,有助于我国蔗区甘蔗花叶病的监测与防控。     

Effects of Jiedu-Qingfei mixture on NF-κB and p38 MAPK pathways in lung tissues of rats with Mycoplasma pneumoniae infection

AIM: To observe the therapeutic effect of Jiedu-Qingfei mixture on Mycoplasma pneumoniae (MP)-infected rat lung tissues and to explore its mechanism. METHODS: SD rats (n=40) were randomly divided into 4 groups:blank control group, model group, Jiedu-Qingfei group and positive control group, with 10 rats in each group. The rats in experimental groups were slowly dripped with 1×10⁹ CFU/L MP solution into their nostrils for 4 d. One rat in each group was sacrificed for MP nucleic acid detection at the second day after inoculation, and the other rats were given gavage therapy. The rats in blank control group and model group were intragastrically given the same volume of normal saline, the rats in Jiedu-Qingfei group were given 8 mL/kg Jiedu-Qingfei mixture daily for 4 weeks, and the rats in psoitive control group were given dexmethasone sodium phosphate (0.5 mg·kg^-1·d^-1). After the experiment, the rats were killed. The serum and bronchoalveolar lavage fluid (BALF) were collected for detecting the levels of interleukin-12 (IL-12), IL-13 and TNF-α by ELISA. The right lung tissues were used for pathological observation and HE staining, while the left lung tissues were used to detect the expression of NF-κB p50, I-κBα and p38 mitogen-activated protein kinase (p38 MAPK) at mRNA and protein levels. RESULTS: The results of MP nucleic acid detection showed that all the rats except blank control group were MP nucleic acid positive, indicating that the rat model of MP infection was successfully established. On the 1st day of the treatment, the pathological scores of the lung tissues in model group and Jiedu-Qingfei group were significantly higher than those in blank control group (P<0.05). After treatment, the pathological scores of the lung tissues in mo-del group were significantly higher than those in blank control group and Jiedu-Qingfei group. The levels of IL-12 in the serum and BALF in model group were significantly lower than those in blank control group after MP infection (P<0.05), while those after treatment with Jiedu-Qingfei mixture were significantly higher than those in model group (P<0.05). The levels of IL-13 and TNF-α in the serum and BALF of MP-infected rats were increased significantly, while those after treatment with Jiedu-Qingfei mixture were significantly lower than those in model group (P<0.05). The mRNA expression levels of NF-κB p50 and p38 MAPK in model group were increased significantly (P<0.01). After treatment, the mRNA expression levels of NF-κB p50 and p38 MAPK were decreased significantly compared with model group (P<0.01). The mRNA expression level of I-κBα in model group was significantly lower than that in control group. After treatment, the mRNA expression of I-κBα in Jiedu-Qingfei group was significantly higher than that in model group (P<0.05). The protein levels of NF-κB p50 and p38 MAPK in the lung tissues of model group were significantly higher than those of blank control group. After treatment, the protein expression of NF-κB p50 and p38 MAPK was decreased significantly. The protein level of I-κBα in model group was significantly lower than that in blank control group, and after treatment with Jiedu-Qingfei mixture, the protein expression level of I-κBα was increased significantly (P<0.05). CONCLUSION: Jiedu-Qingfei mixture may attenuate lung tissue inflammation caused by MP through NF-κB and p38 MAPK pathways.     

中国数量经济学的先驱者之一——周华章

是我国最早的数量经济学博士（1952年，芝加哥大学经济学院），学界对其介绍却并不多。本文根据他的相关论著、史料和档案，并与近几年论述中国经济学史和管理学史的大量文献进行比较，发现他早在1944年就用数理经济学方法，对区位（区域）经济奠基者韦伯（Alfred Weber）的理论做了部分修正。他在芝加哥大学经济学院读博期间写的毕业论文得到了两位获诺贝尔经济学奖大师的指导，经过严谨的分析与论证，对萨缪尔森的理论提出了自己独特的见解。1953年，他还主持国际计量经济学会会长雅各布·马尔沙克委托的研究项目。回国后即与钱学森、许国志、刘源张等为中国运筹学的引进和发展作出了最早的贡献。     

班主任工作浅析

班主任有一颗永不泯灭的童心；慈祥、体贴学生；诚实、公正、虚心、好学、博识、多才；严于律己,宽以待人.老师从内心里整个地接纳学生,跟学生做知心朋友,随时进行心灵的交流,替学生排忧解难,给学生指点人生道路上的迷津,帮学生树立信心,为学生规划美好的前程,使学生身心得到健康的发展.     

农村信息化及城乡信息融合发展的探索

基于农村信息化与信息服务融合发展现状,通过统计数据分析,对农村信息化与城乡融合发展存在的问题进行了分析讨论,并提出了相关对策.     

腐殖酸与EDTA对高铁酸钾降解水中孔雀石绿影响的研究

在高铁酸钾与孔雀石绿的质量比为10∶1,pH值为7.0的条件下,考察腐殖酸与EDTA对高铁酸钾降解水体中孔雀石绿的影响。结果表明,加入少量的腐殖酸和EDTA溶液,孔雀石绿溶液的吸光度降低,有利于高铁酸钾对孔雀石绿的降解;EDTA的加入量过多时,反而抑制高铁酸钾对孔雀石绿的降解;加入2.0 mL腐殖酸和4.0 mL EDTA溶液降解2 h效果较好。     

绵羊FGF10基因克隆、序列分析及其在毛囊发育中的表达分析

本试验旨在获得中国美利奴羊成纤维细胞生长因子10（fibroblast growth factor 10，FGF10）基因的编码区（CDS）全长序列并进行生物信息学分析，随后对FGF10基因在中国美利奴羊毛囊发育过程中的表达特征进行分析，明确其在中国美利奴羊毛囊发育过程中的表达模式，为进一步研究FGF10 mRNA表达水平与中国美利奴羊毛囊生长发育的表达调控机制奠定理论基础。采用PCR扩增获得中国美利奴羊FGF10基因CDS，并克隆到zero PCR@^TM-Blunt进行测序验证；利用实时荧光定量PCR技术检测FGF10在中国美利奴羊毛囊发育过程中的表达差异。结果表明，绵羊FGF10基因CDS长度为696 bp（序列上传GenBank，获得登录号：MT872422），编码231个氨基酸，与牛和山羊的氨基酸序列同源性达100%，存在1个信号肽和1个跨膜结构域，其为分泌通路信号蛋白；实时荧光定量PCR分析表明，FGF10基因在中国美利奴羊毛囊发育过程中均表达，在毛囊发育第85天表达最高，显著高于其他毛囊发育时期（P<0.05）。本研究获得中国美利奴羊FGF10基因完整的编码区序列和毛囊发育过程中的表达特征，生物信息学分析发现，FGF10基因编码区序列具有物种间的保守性，同时FGF10在绵羊毛囊不同发育阶段的皮肤组织中表达，由此表明，FGF10基因可能在绵羊毛囊的生长发育过程中发挥重要的生物学作用。     

硅酸盐解钾菌对含钾矿物的选择性风化机理

从棉花根际土壤中筛选、分离、纯化了硅酸盐解钾菌,进行了硅酸盐解钾菌与7种含钾矿物在厌氧密闭系统中的生物风化解钾试验,探讨了硅酸盐解钾菌对不同含钾矿物生物风化作用的规律。试验结果表明,生物风化反应释放出K+最多的前3个组合是白云母和QY17、黑云母和QY19、白云母和QY19,反应释放出K+的量分别为1 235.76、1 010.71、916.61μg/g。生物风化反应固定K+最多的4个组合是黑云母和QY4、蒙脱石和QY3、黑云母和QY10、高岭石和QY17,反应中含K矿石固定K+的量分别为78.35、39.92、32.71、22.56μg/g。形成差异的原因可能是硅酸盐解钾菌(包括其次生代谢物)与含钾矿物的晶体结构之间的双向选择过程。硅酸盐解钾菌浓度越大,硅酸盐解钾菌类群对矿物生物风化作用有选择性倾向越明显。造成硅酸盐解钾菌的解钾数量、速率的差异的原因是界面交换过程的不同,机理是硅酸盐解钾菌(次生代谢物)与含钾矿物之间空间构效关系(CQSAR)。风化作用是硅酸盐细菌剥蚀作用、机械破碎、次生有机酸解钾过程交替循环所产生的。腐殖酸的加入促进了硅酸盐解钾菌解钾的过程,延长了解钾时间,同时向硅酸盐解钾菌提供C、N养分。