4LMZ160型履带式苎麻联合收割机的研究

分析了我国苎麻联合收割机现状及存在的问题,设计了适合我国苎麻主产区收获作业的履带式苎麻联合收割机,并对样机的关键部件进行了详细说明。该机一次可完成割幅160mm收割,整机转弯半径小,操作方便,对麻地高垄有较好适应性。其整机结构配置新颖独特,使用半喂入稻麦联合收获机底盘,采用全液压传动技术直接驱动苎麻收割机行走和机具作业,可一次性完成切割、输送、收集功能。田间性能测试结果表明:该机漏割率、割茬高度、作业小时生产率等各项性能指标均到达设计要求。     

我国蔬菜育苗产业现状及发展动态

蔬菜育苗是蔬菜生产中的关键环节之一,不仅可以节约用种量、增加复种指数,而且便于集约化管理,在我国有广阔的市场前景。为此,阐述了我国目前主要的几种育苗方法及相关技术,指出现阶段我国蔬菜育苗产业存在着育苗企业良莠不齐、缺乏规范化管理、育苗方法技术滞后和劳动者技术水平低等问题,并有针对性地提出了解决措施。目前,随着我国农业种植结构的调整,蔬菜育苗产业正向基质低廉化、育苗工厂化、育苗专业化及种苗标准化等方向发展。     

区域农业水资源恢复力可变模糊评价模型

区域农业水资源系统是与自然及人类活动紧密联系的复杂适应系统,不断与周围环境发生物质、能量和信息因素方面的交换和作用。以黑龙江省农垦红兴隆管理局12个农场为研究基点,运用主成分-相关分析法筛选评价指标,构建农业水资源恢复力评价指标体系,采用CRITIC法确定指标权重,结合可变模糊模型评价方法对其农业水资源系统恢复力进行评价,并利用ArcGIS技术对其进行分区,结果表明:双鸭山、八五三、北兴和八五二农场的农业水资源恢复力为Ⅱ级,饶河、二九一、五九七、红旗岭、友谊、江川、宝山和曙光的农业水资源恢复力为Ⅲ级。研究成果揭示了当地农业水资源系统力恢复情况,为农业水资源系统恢复力研究提供了一种新的研究模式。     

低温条件下组合式生态浮床系统净化微污染水体的特性研究

为研究低温对生态浮床水质净化效果的影响,引入陶粒作为浮床的基质,构筑了美人蕉-陶粒基质组合式生态浮床系统,研究在低温条件下其对微污染水体水质净化的效果特性。结果表明,在进水温度为0.5~15℃,进水DO浓度为4.94~6.65mg/L,水体交换时间为7d下,该生态浮床系统对水体中NH+4-N、NO-3-N、NO-2-N、TN、COD和色度的平均去除率为36.30%、77.37%、50.34%、52.56%、16.89%和70.99%。当水体的温度低于5.0℃,该生态浮床系统对水体中NH+4-N、NO-2-N、TN、COD和色度的去除效果均有所下降。     

制种玉米密度对土壤水分及产量构成的影响研究

通过田间试验,就制种玉米密度对土壤水分、农艺性状、产量构成及产量的影响进行了研究分析。结果表明:1在拔节期以前,低密组的土壤含水量比高密组的高;在拔节期到灌浆期,高密组的比低密组的高。在整个生育期,拔节期前土壤含水量比较高,而后逐渐降低,吐丝期达到最低,然后又逐步上升。2在一定密度范围内,制种玉米株高、亩产量随着密度的增大而增加单株产量产量相反;叶长、穗粗、穗粒数先随着密度的增大而减小,后随着密度的增大而增大;叶宽、穗长、百粒重、出籽率先随着密度的增大而增加,后随着密度的增大而减小;叶面积、茎粗、穗位先随着密度的增大而减小,后随着密度的增大而增加,然后又随着密度的增大而减小,秃顶变化规律相反。     

单片机技术在自动给料系统中的应用

文章设计了基于单片机控制的送料机自动送料机控制系统,论述了单片机AT89C51在实现其生产过程控制的自动给料系统的设计方法。     

不同灌溉方式下冬小麦穗部性状与产量关系的试验研究

采用田间试验,以豫麦69为试验材料,研究了不同水分处理下常规灌溉和一体化垄作沟灌的冬小麦产量与穗部性状的相互关系。结果表明,同常规灌溉方式相比,一体化垄作沟灌方式下,冬小麦的穗粒数、籽粒质量及产量分别增加了5.5356%、7.5489%、7.7454%,但穗数减少了0.4302%。常规灌溉和一体化垄作沟灌方式下,产量与穗数、穗粒数以及籽粒质量均正相关,但一体化垄作沟灌方式下的相关系数较常规灌溉方式大。一体化垄作灌溉有利于改善农田小气候、发挥作物的边行优势和提高小麦产量。     

渗灌对日光温室番茄栽培环境的影响

研究了渗灌和漫灌对日光温室番茄栽培环境及番茄产量的影响。结果表明,渗灌下,土壤密度比漫灌低7.59%,差异极显著;土壤总孔隙度比漫灌高9.72%,差异显著;土壤黏粒和粉粒高于漫灌,而砂粒和细粗砾低于漫灌;观测时段内,渗灌下平均气温、10cm处土壤平均温度较漫灌分别高1.55℃、0.86℃,地表平均温度比漫灌低0.14℃;渗灌下温室空气相对湿度较漫灌低11.86%,以10:00—20:00差值最大;渗灌下番茄产量比漫灌高8.60%,且差异显著。     

Residue Detection of Tetracyclines in Eggs by High Performance Liquid Chromatography

The study was aimed to establish the method of simultaneous detection of four kinds of tetracyclines,including oxytraoycline,tetracycline,chlortetracycline and doxyeycline in eggs by high performance liquid chromatography (HPLC).The eggs samples were detected with HPLC after through the procedure of extraction of 0.1 mol/L Na₂EDTA-Mcllvaine buffered solution,purification of Oasis MAX solid-phase extraction column,gradient elution of taking acetonitrile-0.01 mol/mL trifluoroacetic acid as mobile phase,separation with reverse liquid chromatography.The results showed that the calibration curves of four kinds of tetracyclines were linear correlated in the concentration range of 30 to 1 000 ng/g which the limits of detection was 10 ng/g and the limit of quantification was 50 ng/g.The average recoveries were 67.3% to 81.4%,relative standard deviations of intraday was 2.7% to 14.3%,relative standard deviations of inter-day was 0.9% to 5.0%.This mothod established in this study could simultaneously detect oxytetracycline,tetracycline,chlortetracycline and doxycycline drug residues in egg and it had high sensitivity,accuracy and precision.The method was rapid and simple to operate.     

Preparation and Identification of Canine Parvovirus NY Strain VP2 Protein Polyclonal Antibody

This study was aimed to prepare canine parvovirus (CPV) VP2 protein polyclonal antibody.The recombinant expression vector pET28a-CPV-VP2 was constructed and transfromed into E.coli BL21 (DE3),the expression of recombinant proteins was induced by IPTG from which the fusion protein was identified by SDS-PAGE.The target protein was purified and emulsify with adjuvant,the prepared immunogen was inoculated into rabbit by subcutaneous injections to prepare of VP2 protein specific polyclonal antibody.The immuno-activity,titers,neutralization titers of the prepared polyclonal antibody were determined by immunoperoxidase monolayer assay (IPMA).The results showed that the expressed recombinant protein VP2 (rVP2) existed in the form of inclusion body with a molecular weight of 72 ku.The prepared polyclonal antibody titer was 1 600 dilution,the virus titer was 10⁷ TCID₅₀/mL,the neutralizing titer was 1∶2 884.The antibodies showed specific reaction with CPV.In conclusion,rVP2 specific polyclonal antibody showed wonderful immunocompetence,specificity and neutralizing activity,providing foundation for the development of genetic vaccine and clinical therapeutic method.