南帕斯凝析油卸船的安全措施

针对南帕斯凝析油接卸作业过程中易产生较高含量有毒气体的问题,分析了凝析油的基本性质和硫化物分布情况,以识别其有毒气体成分.描述了接卸作业前和码头接卸作业两个阶段的注意事项:接卸作业前应对各个作业环节进行风险识别,制定应急方案,并确保设备完整;码头接卸作业前先进行作业准备,划定作业警戒区且保证消防通道畅通,接卸作业时,持续进行硫化氢检测,接卸作业后,及时对管道进行置换.最后,指出检尺口和卸船舱口为主要泄漏风险部位,提出了解决措施.     

北京油鸡与贵妃鸡杂交效果研究

本研究以北京油鸡和贵妃鸡为素材,比较北京油鸡♂×北京油鸡♀(YY)、贵妃鸡♂×贵妃鸡♀(GG)、北京油鸡♂×贵妃鸡♀(YG)、贵妃鸡♂×北京油鸡♀(GY)4种组合的外貌、体重、屠宰性能和肉质性状.结果表明:杂交后代凤头、胡须、毛腿、双五趾个体比例分别是99.4％、88.1％、95.2％和72.0％;6～20周体重显著高于贵妃鸡(P＜0.01),16周屠宰率、半净膛率、全净膛率和胸肌率高于北京油鸡(P＜0.01).以北京油鸡为母本的杂交组,同周龄体重有高于北京油鸡为父本杂交组的趋势,且屠宰率和胸肌率较高(P＜0.05),为最佳组合.     

规模养蚕新技术的研究Ⅰ.大棚养蚕温湿度对蚕茧产质量的影响

试验调查了大棚养蚕春、夏大蚕期与蔟中的温湿度变化,以探索有利于大棚养蚕的饲养技术与小气候调节技术.棚内温湿度变化对蚕茧产质量的影响比较分析表明,春期5龄后期和上蔟初期,35～38.8℃的高温对蚕茧产质量有较大影响;夏蚕期棚内温度明显高于春蚕期,最高超过40℃,连续高温持续时间长,昼夜温差大.根据春、夏期不同的气候特点,春期大棚上蔟初期要重点进行降温排湿,夏期重点进行降温.     

家蚕有滞育多化性品种滞育卵复式冷藏继代法的研究

利用上年中秋制种的滞育卵经复式冷藏处理,到当年夏蚕期饲养,夏制种再经中秋蚕期饲养,进行了有滞育多化性品种的省力保种试验.夏蚕期其生命力较对照组低1.2%~1.9%,生种率上升16.0%,差异达显著程度.中秋蚕期生命力高1.0%,生种率低0.9%,完全恢复正常.重复试验,结果一致.有滞育多化性品种用滞育卵复式冷藏处理一年二次省力保种是可行的.     

浅析关于丰都丝绸行业的治企方略

1　行业现状丰都丝绸行业共有 9个不同所有制的企业 ,固定资产 7,0 0 0万元以上 ,从业人员2 ,50 0人左右 ,中级以上科技人员 30人 ,其中高级农艺师、政工师 5人。1 .1　县丝绸公司公司成立于 1 983年 ,属事业单位、企业管理的农工商贸一体化的经济组织 ,是茧丝绸行业的管理部门 ,机关设 7科 1室 ,1 9个乡镇蚕业站 ,2 6个茧站。现有员工 2 1 0人 ,退休干部 37人 ,离岗 35人。有 2 3个养蚕乡镇 ,桑园面积 2 ,0 0 0公顷 ,栽桑 1亿株 ,投产桑 8,0 0 0万株 ,全县年产茧能力 3万担 ,年交税 1 0 0余万元。1 .2　丰都丝厂该厂始建于 1 987年 ,属国有…     

DNA Barcoding:An Effective Tool for Species Identification of Lepidopteran Oak Pests

[Objective] The paper was to improve the efficiency and accuracy of early forecast of Lepidopteran oak-infesting pests.[Method] DNA barcoding technique was established for quick species identification using mitochondrial cytochrome C oxidase subunit Ⅰ(COⅠ) as the standard gene.This barcoding technique was used to amplify and sequence genomic DNA samples from eggs and pupae of 11 species of Lepidopteran pests collected from oak.[Result] The DNA barcoding standard genes of 594-708 bp were determined from eggs and pupae of Lepidopteran insects.There were differences of 0-2 bases in DNA barcode sequences between conspecific eggs and pupae,with the sequence identity of 99.7%-100%.The average content of A,T,G and C of DNA barcode sequences from Lepidopteran insects were 30.7%,38.5%,14.9% and 15.9%,respectively.The obtained DNA barcode sequences had 91.4%-100% identity and 0-8.6% difference degree with GenBank-deposited DNA barcode sequences from organisms of the genetically-closest relationship.Among them,DNA barcode sequences from egg and pupa samples of 10 Lepidopteran insects(No.1-20) had 99%-100% identity and 0-1.0% difference degree with homologous sequences in GenBank database,while the remaining samples(No.21-22) had high difference degree(8.6%) with homologous sequences.[Conclusion] The established DNA barcoding technique is an effeetive tool for species identification of Lepidopteran pests using genomic DNA from eggs and pupae of Lepidopteran insects.     

A cluster of two psittacosis cases among women farmers exposed to Chlamydia psittaci-infected domestic poultry in Zhejiang Province,China

A cluster of Chlamydia psittaci (C. psittaci) cases was reported in Zhejiang Province, China, 2019. This study evaluates the extent of the outbreak and determines the source of infection. Real-time PCR and sequencing of the ompA gene of C. psittaci were performed to identify the cases, the domesticated poultry and close contacts. The index patient was a 76-year-old woman with chronic vertigo, and Case 2 was a 64-year-old female farmer with herpes zoster. Both women bought psittaci-infected chickens or ducks from the same mobile street vendor and raised them for 10 days and 23 days before fever onset. There were no direct contact between the two women. C. psittaci test was positive for the two patients, one sick chicken, three healthy ducks and the vendor's chicken cage. Phylogenetic analysis showed that all seven C. psittaci positive samples carried identical ompA genotype A of C. psittaci. Of all of the patients' 148 close contacts, none tested positive for C. psittaci, or developed acute respiratory symptoms. Both patients were discharged after a 4-week hospital stay. In conclusion, the source of this cluster was the poultry infected with C. psittaci, which occasionally cause infections in farmers, but inter-human transmission seems unlikely.     

宿主域扩大的重组救活昆虫杆状病毒表达载体的构建及外源基因的表达

通过克隆的家蚕核多角体病毒解旋酶基因DNA与重组救活可线性化的苜蓿尺蠖核多角体病毒基因工程载体病毒 (BacPAK6 )DNA在昆虫细胞中发生重组 ,经累代筛选获得了既可感染家蚕又可感染秋粘虫细胞Sf 2 1的宿主域扩大的昆虫杆状病毒表达载体 (HyBacPAK6 )。HyBacPAK6DNA经Bsu36Ⅰ酶切后与含植酸酶基因的转移载体pVL1393 phy在家蚕细胞中重组后 ,通过蓝白斑筛选发现重组率可达 90 %以上。然而以杂交病毒为载体的外源基因表达量仅为以BmNPV为载体病毒的表达量的 2 0 %左右。分析认为HyBacPAK6可用于表达一些对蚕体有害的外源基因。     

体外评定酸化剂作用效果的方法探讨

文章主要论述了体外法评定酸化剂作用效果的指标和评定方法。