几种绿色饲料添加剂在肉鸡生产上的应用效果

选1日龄AA肉鸡390只,分成13组,分别添加不同种类和不同种类组合的绿色饲料添加剂。试验结果表明,益生素能显著(p<0.05)提高肉鸡的生产性能,改善肉品质。     

利用土壤筛选紫花苜蓿高效共生根瘤菌的初步研究

采用西北地区土壤试管栽培法对12株不同地区来源的根瘤茵和2个紫花苜蓿Medicago sativa品种(品系)进行接种效果的研究，旨在使筛选结果尽量接近实际生产环境，筛选出符合实际效果的高效共生菌株。结果表明，紫花苜蓿与根瘤菌之间表现出共生效果的多样性。绝大多数接种根瘤菌的紫花苜蓿在总瘤数、有效瘤数、地上部干质量方面与不接种的对照相比分别增加了7％～240％，10％～367％，7％～150％。根瘤菌与紫花苜蓿品种之间存在着互作关系，且受土壤因子尤其是土壤养分状况的影响。初步筛选出的与2个紫花苜蓿品种(品系)最佳共生匹配的根瘤菌菌株分别是：中苜一号的73317，01006，01055；金皇后的83092，01006，01055。     

优质肉鸡繁育体系的效益评估

近十多年来，我国优质肉鸡的生产方兴未艾，许多育种公司和科研院所不断推出新品系。为充分发挥新品系的遗传潜力，探求优质肉鸡最佳的繁育生产模式具有重要意义。由于不同的品系及其杂种后代在不同的性状上各有优缺点，很难用生产性能进行直接比较，而适合用育种规划的方法通过经济学指标进行评价。系统分析通过把生产系统抽象概念化并用数学手段模型化的方法，     

母牛一胎双犊技术的研究

选择9头母牛先行人工授精、7天后再移植冷冻胚胎以生产双犊。试验结果表明,母牛产双犊达44.44%(P<0.01)。提示:采用A(I人工授精)+ET(胚胎移植)是提高母牛双犊率的有效技术措施之一。     

核酸疫苗研究进展(下)

Sato等报道，在质粒载体上引入大肠杆菌Amp^ 抗性基因(内含有6核苷酸片段的ISS免疫增强序列)，真皮免疫小鼠后ISS增强CTL和Th1细胞的免疫反应。有人提出利用含有病毒免疫原性基因的基因大片段进行基因免疫，以弥补单基因免疫活性的不足。将协同因子如IL-2、IL-12、TCA等的表达质粒与抗原表达质粒混合注射可使Th1型细胞免疫增强，而GMcsf能明显加强体液免疫，     

日粮中添加牛至油对河西绒山羊育肥性能的影响研究

牛至精油对家畜生产性能和免疫力的提高有重要的影响。通过在日粮中添加牛至精油育肥河西绒山羊,研究其对河西绒山羊生长性能、屠宰性能及胴体品质的影响。对照组饲喂基础日粮,试验组在饲喂的基础日粮中分别添加4和7 g宜生饲宝(含牛至精油的添加剂),4和7 g宜生饲宝中牛至精油的含量分别为52和91 mg。对照组和试验组均为同月龄、同体重的河西绒山羊羯羊,试验组和对照组均设3个重复,每个重复5只羊。育肥期为90 d,每30 d为1个阶段。试验结果表明:育肥全期,对照组、4 g组和7 g组河西绒山羊平均日增重分别为96.30、172.22和169.82 g·d^-1,4 g组和7 g组分别显著高于对照组(P<0.05),4 g组和7 g组无显著差异(P>0.05);屠宰性状,胴体重对照组、4 g组和7 g组分别为20.24、24.18和23.90 kg,无显著差异(P>0.05),屠宰率对照组、4 g组和7 g组分别为48.86%、51.21%和51.56%,4 g组和7 g组分别显著高于对照组(P<0.05),4 g组和7 g组无显著差异(P>0.05),胴体净肉重对照组、4 g组和7 g组分别为12.90、16.27和15.99 kg,4 g组和7 g组分别显著高于对照组(P<0.05),4 g组和7 g组无显著差异(P>0.05);肉质性状,大理石纹4 g组和7 g组分别显著高于对照组(P<0.05),4 g组和7 g组无显著差异(P>0.05),pH、熟肉率、失水率、嫩度、蒸煮损失对照组、4 g组、7 g组间均无显著差异(P>0.05)。日粮中添加牛至油可以显著提高河西绒山羊的育肥性能,本试验日粮中添加4 g宜生饲宝(含牛至精油52 mg)效果最佳。     

土壤易氧化有机碳与溶解性有机碳对荒漠草地沙漠化过程中土壤碳库变异的表征

以干旱、半干旱地区荒漠草地不同沙漠化阶段土壤为研究对象,研究不同沙漠化阶段土壤易氧化有机碳与溶解性有机碳含量和分配比例变异规律,分析不同沙漠化阶段土壤碳库指数变化,探讨荒漠草地沙漠化过程中土壤易氧化有机碳与溶解性有机碳对土壤碳库的表征作用。结果表明,随着荒漠草地沙漠化程度的加剧,易氧化有机碳含量表现出一定的波动性,但整体呈下降趋势,溶解性有机碳含量呈线性下降。易氧化有机碳和溶解性有机碳分配比例均在荒漠草地达到最大值,在半固定沙地达到最小值。利用易氧化有机碳含量计算的土壤碳库管理指数随荒漠草地沙漠化程度增加表现出先下降后上升趋势,利用溶解性有机碳含量计算的土壤碳库管理指数呈线性下降趋势。易氧化有机碳、溶解性有机碳含量与土壤有机碳均显著正相关,但溶解性有机碳的相关系数略高于易氧化有机碳。通过比较活度敏感指数和碳库管理指数敏感指数发现,荒漠草地逆向演替至固定沙地过程中,易氧化有机碳的各项敏感指数均高于溶解性有机碳。固定沙地演替至流动沙地过程中,溶解性有机碳的各项敏感指数均高于易氧化有机碳,表明易氧化有机碳能够较好地表征荒漠草地沙漠化前期土壤碳库变化,而荒漠草地沙漠化中期和后期利用溶解性有机碳表征效果更好。     

Amino acid profiles of rumen undegradable protein: a comparison between forages including cereal straws and alfalfa and their respective total mixed rations

Optimizing the amino acid (AA) profile of rumen undegradable protein (RUP) can positively affect the amount of milk protein. This study was conducted to improve knowledge regarding the AA profile of rumen undegradable protein from corn stover, rice straw and alfalfa hay as well as the total mixed ratio diets (TMR) based on one of them as forage source [forage‐to‐concentrate ratio of 45:55 (30% of corn stover (CS), 30% of rice straw (RS), 23% of alfalfa hay (AH) and dry matter basis)]. The other ingredients in the three TMR diets were similar. The RUP of all the forages and diets was estimated by incubation for 16 hr in the rumen of three ruminally cannulated lactating cows. All residues were corrected for microbial colonization, which was necessary in determining the AA composition of RUP from feed samples using in situ method. Compared with their original AA composition, the AA pattern of forages and forage‐based diets changed drastically after rumen exposure. In addition, the extent of ruminal degradation of analysed AA was not constant among the forages. The greatest individual AA degradability of alfalfa hay and corn stover was Pro, but was His of rice straw. A remarkable difference was observed between microbial attachment corrected and uncorrected AA profiles of RUP, except for alfalfa hay and His in the three forages and TMR diets. The ruminal AA degradability of cereal straws was altered compared with alfalfa hay but not for the TMR diets. In summary, the AA composition of forages and TMR‐based diets changed significantly after ruminal exposure, indicating that the original AA profiles of the feed cannot represent its AA composition of RUP. The AA profile of RUP and ruminal AA degradability for corn stover and rice straw contributed to missing information in the field.     

Methyl donors dietary supplementation to gestating sows diet improves the growth rate of offspring and is associating with changes in expression and DNA methylation of insulin‐like growth factor‐1 gene

The study aimed to investigate the effects of maternal dietary methyl donors on the performance of sows and their offspring, and the associated hepatic insulin‐like growth factor‐1 (IGF‐1) expression of the offspring. A total of 24 multiparous sows were randomly fed the control (CON) or the CON diet supplemented with methyl donors (MD) at 3 g/kg betaine, 15 mg/kg folic acid, 400 mg/kg choline and 150 μg/kg VB₁₂, from mating until delivery. After farrowing, sows were fed a common lactation diet through a 28‐days lactation period and six litters per treatment were selected to be fed until at approximately 110 kg BW. Maternal MD supplementation resulted in greater birthweight (p < 0.05) and increased the piglet weights (p < 0.01) and litter weights (p < 0.05) at the age of day 28, compared with that in CON group. The offspring pigs in the MD group had greater ADG (p < 0.05) and tended to lower F:G ratio (p = 0.07) compared with that of CON group from day 28 to 180 of age. The offspring pigs from MD group had greater serum IGF‐1 concentrations and expressions of hepatic IGF‐1 gene and muscular IGF‐1 receptor (IGF‐1r) protein at birth (p < 0.05), and greater hepatic IGF‐1 protein (p = 0.03) and muscular IGF‐1r gene expressions (p < 0.05) at slaughter, than that from the CON group. Moreover, the methylation at the promoter of IGF‐1 gene in the liver of newborn piglets and finishing pigs was greater in the MD group than that of the CON group (p < 0.05). In conclusion, maternal MD supplementation throughout gestation could enhance the birthweight and postnatal growth rate of offspring, associated with an increased expression of the IGF‐1 gene and IGF‐1r, as well as the altered DNA methylation of IGF‐1 gene promotor.