我国丝绸面临的困境及成因浅析

丝绸业是以茧丝绸为纽带 ,以出口创汇为主的跨越农工贸的外向型行业 ,现在我国的蚕茧和生丝产量分别约占世界总产量的78%和 72 % ,丝类、绸缎和丝绸服饰的出口量分别约占世界贸易的 90 %、50 %和 45% ,1 950～ 1 998年间丝绸出口创汇达 42 2 .1 2亿美元 ,在世界丝绸业和国民经济中占有重要的地位。1　我国丝绸业面临的困境80年代后期 ,我国丝绸行业高速发展 ,产量大幅攀升 ,出口量迅猛增加 ,但至 90年代中期 ,全行业发生前所未有的亏损 ,近来 ,以加入ＷＴＯ为契机 ,行业情况有所好转 ,但也仍在困境中艰难跋涉 ,发展前景不容盲目乐观。自 1 9…     

强化防微措施 提高蚕种质量

衡量蚕种质量的主要指标有蚕品种的杂交率、良卵率、家蚕微粒子病的带毒率,其中毒率的高低对蚕种质量影响很大.目前,我国在有望加入世界经济贸易组织的利好消息刺激下,茧丝绸行业有所复苏,蚕业又将进入一个新的发展时期.在本行业处于衰兴交替之时,我们种场又将面临一次新的挑战.种场只有加强对原蚕饲养基地的技术投入和资金投入,采取有效的防微措施,提高蚕种质量,才能在竞争中获胜.     

饲料钙测定中原子吸收法和高锰酸钾滴定法的比较

在国家标准中，饲料中钙的测定方法是高锰酸钾滴定法。其方法原理是：将试样中有机物破坏，钙变成溶于水的离子，用草酸铵定量沉淀，用高锰酸钾法间接测定钙含量。此方法前处理较繁琐，前后需三天时间，检测周期较长。对于大批量的样品检测的速度带来一定的影响。原子吸收法测定比高锰酸钾滴定法更简便和直接，并且更精确。其方法原理为：样品经湿法消化，分解有机质后，将钙元素溶解在稀酸中，将溶液直接吸入空气－乙炔火焰中原子化，并在光路中测定钙原子对特定波长谱线的吸收。1 仪器和试剂1.1 仪器原子吸收分光光度计(美国瓦里安公司，…     

黄芪注射液对犬心脏双向变时作用的初步观察

为了观察黄芪注射液对正常犬和二尖瓣关闭不全病理模型 (MR)犬的变时作用 ,并探讨其机制 ,在异氟烷吸入麻醉下 ,对正常及外科方法制作的犬亚急性二尖瓣关闭不全模型 (术后 5 0天后 )一次性静脉推注含生药 2 g/ m L的黄芪注射液 1 .2 5 m L/ kg,通过体表心电图测定心率和 PQ、QRS、RR、QT,并计算 QTC(QT/ RR)间期。在正常犬 ,开始注射黄芪注射液后 ,心率出现先减少后恢复再持续减少和显著变化。 MR模型犬开始注射液后 ,心率出现先升高后恢复再持续升高的显著变化。 MR模型犬的心率减慢变化与 RR、PQ、QT、QTc呈高度显著负相关 (P<0 .0 1 )。表明黄芪注射液对正常比格犬 ,具有加快心率的正性变时作用。对二尖瓣闭锁不全 (MR)模型犬具有减缓心率的负性变时作用。黄芪注射液的变时作用似与机体的机能状态有关 ,呈现双向调节作用。     

日粮添加免疫生长促进剂C96对雏鸡若干血液指标的影响

选择１２０只１日龄ＡＡ商品健康雏鸡,随机分为４组,每组３０只。初步观察了日粮添加免疫生长促进剂Ｃ９６对血液中红细胞总数（ＲＢＣ）、比容（ＰＣＶ）、血红蛋白含量（Ｈｂ）、网织红细胞比例（ＲＣＣ）、白细胞总数（ＷＢＣ）等的影响。结果表明：肉雏鸡在１５ｄ时,日粮添加Ｃ９６为１１ｍｇ／ｋｇ,饲料的Ｃ９６组和疫苗－Ｃ９６组,与对照组和疫苗组比较,ＲＢＣ和Ｈｂ增高,ＷＢＣ显著下降,ＲＣＣ降低,ＰＣＶ无明显规律性变化;３０ｄ和４５ｄ时,添加Ｃ９６组和疫苗－Ｃ９６组的ＲＢＣ、Ｈｂ和ＰＣＶ,与对照组和疫苗组基本相近,ＷＢＣ和ＲＣＣ均比对照组和疫苗组低或明显低。但３０ｄ时疫苗组的ＷＢＣ比对照组高。整个试验期,ＲＢＣ、ＷＢＣ和ＰＣＶ随日龄的增长呈上升趋势,ＲＣＣ呈波动性下降。     

Effect of Fermentation Bed with Spent Mushroom Substrate of Pleurotus eryngii on Weaning Piglets

[Objective] The paper was to investigate effects on fermentation bed temperature,growth performance,diarrhea rate and digestive en-zyme activity of weaning piglets by using spent mushroom substrate of Pleurotus eryngii as padding.[Method] A total of 120 weaning piglets(Duroc × Landrace ×Yorkshire) with average initial body weight of(8.0 ±0.5)kg were allocated to five dietary treatments in a randomized complete block design for 42 d,each of which was replicated three times with eight piglets per replicate(half male,half female).The padding for control group was(50% sawdust +50% rice husk);experimental group Ⅰ 100% spent mushroom substrate;experimental group Ⅱ(15% sawdust +15% rice husk +70% spent mushroom substrate);experimental group Ⅲ(25% sawdust +25% rice husk +50% spent mushroom substrate);experimental group Ⅳ(35% sawdust +35% rice husk +30% spent substrate).[Result] There was no significant difference in surface temperature of fermentation bed between experimental groups and control group(P0.05).Compared with the control group,the temperature under 20 cm of fermentation bed in ex-perimental groups I,Ⅱ and Ⅲ increased significantly(P0.05).Except for experimental group Ⅳ,other three experimental groups had higher aver-age daily gain(P0.05) and experimental group Ⅰ had higher average daily feed intake(P0.05) compared to the control group.The diarrhea rate and mortality of weaning piglets in experimental groups Ⅱ,Ⅲ and Ⅳ were significantly decreased compared with the control group(P0.05).Compared with the control group,other three experimental groups had higher digestive enzyme activity in duodenal contents except for experimental group Ⅳ(P0.05).[Conclusion] Spent mushroom substrate of P.eryngii can be used as fermentation bed padding,and the optimal proportion was experimental group Ⅲ.     

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.     

不同投喂方式对革胡子鲶消化酶的影响

在（25±1）℃水温、自然光照条件下,设3种投喂方式饲养革胡子鲶（clarias leath-er）：第1种连续投喂整个试验期间不间断,第2和3种分别连续投喂3、7 d 后饥饿1 d,3种方式分别以R0（对照组）、R1/3、R1/7表示,试验周期共45 d。结果显示：R0、R1/3和R1/7组胃、后肠和肝脏中蛋白酶活性影响差异不显著,但前肠和中肠内蛋白酶活性影响存在差异(P<0.05)。R0、R1/3、R1/7组的胃、前肠、中肠、后肠和肝脏中淀粉酶影响不显著,R0、R1/3、R1/7的胃、前肠和肝脏内脂肪酶活性影响差异显著(P<0.05),而R0、R1/3、R1/7组中肠和后肠中脂肪酶活性影响差异不显著(P>0.05)。     

在生物经济中发展柞蚕产业

2009亚太国家生物经济会议《亚太生物经济项目册》中有五个蚕业项目,充分显示了我国蚕业在生物经济中的地位和发展潜力。本文引入生物经济的概念,介绍了我国柞蚕生物工程的概况,提出用工业化理念发展蚕业,要用现代信息产业改造传统蚕业,在生物经济领域突破发展柞蚕产业。     

Molecular cloning and expression analysis of a CXC chemokine gene from large yellow croaker Pseudosciaena crocea

In the present study, we report the cloning of a CXCL12 chemokine gene homologue from the large yellow croaker Pseudosciaena crocea (LycCXCL12). The complete cDNA of LycCXCL12 is 678 nucleotides (nt) encoding a protein of 97 amino acids (aa), with a putative molecular weight of 11.1 kDa. The deduced LycCXCL12 contains a 22-aa signal peptide and a 75-aa mature polypeptide, which possesses the typical arrangement of four cysteines as found in other known CXC chemokines. It shares 57-68% and 32-36% aa sequence identities to known CXCL12 chemokines in fish species and other vertebrates, respectively. The LycCXCL12 gene was constitutively expressed in all tissues examined although at different levels. Upon induction with poly(I:C) or inactivated trivalent bacterial vaccine, LycCXCL12 gene expression was significantly up-regulated in gills, liver, kidney, spleen and blood at 24 h after stimulation. Time course analysis using real-time PCR showed that LycCXCL12 gene expression reached peak level in spleen and kidney at 12 h or in gills at 24 h post-induction by poly(I:C), while its expression increased to the highest level in kidney at 24h or in gills and spleen at 48 h post-induction by bacterial vaccine, indicating that LycCXCL12 gene expression was differentially regulated by poly(I:C) and bacterial vaccine.