欧拉羊在甘南半农半牧区与山谷型藏羊的适应性对比

从甘南州玛曲县河曲马场引进欧拉羊种公羊30只,投放到卓尼县的半农办牧区进行放牧,观察欧拉羊的行为表现、生长发育、生理生化指标、繁殖性能、发病与死亡情况,结果各项指标正常,适应性良好,充分发挥了种公羊的生产性能,且具有杂交改良山谷型藏羊的优势,引种获得成功。     

欧拉型藏羊杂交改良山谷型藏羊F_1代生长发育对比分析

为研究甘南地区欧拉羊杂交改良山谷型藏羊效果,对欧拉羊与山谷型藏羊杂交试验组和山谷型藏羊本交对照组所产后代的初生、3月龄、6月龄、12月龄、18月龄的体尺、体重进行了跟踪测定,并对不同年龄段杂交后代与对照组后代进行了对比分析和差异显著性检验。结果表明：杂交F1代初生、3月龄、6月龄、12月龄、18月龄的体尺、体重极显著的高于对照组（P〈0.01）,初生、18月龄管围差异显著,3月龄、6月龄、12月龄管围差异不显著（P〉0.05）。     

草莓新品种引种试验

对引进的74个国内外草莓新优品种进行栽培试验比较研究,筛选出鬼怒甘、公四莓、法兰地和麦特来4个优于主栽种丰香、适宜在我省推广栽培的品种。     

Effect of seed coverings and seed pretreatments on the germination response of <Emphasis Type="Italic">Alnus glutinosa</Emphasis> and <Emphasis Type="Italic">Betula pubescens</Emphasis> seeds

The germination of common alder (Alnus glutinosa (L.) Gaertn.) and downey birch (Betula pubescens Ehrh.) seeds is often poor in bare-root nurseries. The effect of a variety of seed coverings and a few seed pretreatments on seedling emergence was examined in this study in an attempt to address this problem. Seeds of each species were sown in trays containing nursery soil, covered with grit, gravel, sand, combinations of these coverings, a hydromulch or a sealed plastic cloche and then incubated for 6 weeks at 17–20°C. The grit combined with sand or gravel, the hydromulch and the cloche increased seedling emergence when compared with the standard grit. In another experiment, seeds of each species were fully imbibed (FI) (>50% moisture content, MC), as per standard practice, or adjusted to target MC (TMC) (30–35% MC) levels, and then chilled to release dormancy. Some seeds of each MC treatment were primed at 20°C for 2 days following chilling, after which all seeds were evaluated in laboratory tests and a nursery trial. Germination potential of the FI seeds declined in the lab tests by the second test date, which was reflected in low seedling emergence in the nursery in birch. The primed FI seeds of alder germinated most rapidly in the nursery, but other effects were not significant. Seedling emergence was better in the nursery in response to the TMC than the FI pretreatment in birch.

The effects of canthaxanthin on porcine oocyte maturation and embryo development in vitro after parthenogenetic activation and somatic cell nuclear transfer

The objective of this study was to examine the effects of canthaxanthin (Cx) treatment during in vitro maturation (IVM) of porcine oocytes on embryonic development after parthenogenetic activation (PA) and somatic cell nuclear transfer (SCNT), on intracellular glutathione (GSH) and reactive oxygen species (ROS) levels in mature oocytes, and on gene expression in both PA‐ and SCNT‐derived blastocysts. To determine the optimal effective concentration of Cx, porcine oocytes were cultured in IVM medium supplemented with various concentrations (0, 20, 40 and 80 μM) of Cx for 22 hr. Compared to other groups, supplementation with 40 μM Cx significantly improved blastocyst formation rates after PA (p < .05), but no significant differences were observed among groups in total blastocyst cell numbers. Subsequently, oocytes were cultured in IVM medium supplemented with or without 40 μM Cx. Oocytes treated with 40 μM Cx showed significantly increased cleavage and blastocyst formation rates after SCNT compared to the control group (p < .05). Moreover, significantly increased intracellular GSH and reduced ROS levels were observed in the Cx‐treated group (p < .05). In addition, both PA‐ and SCNT‐derived blastocysts from the 40 μM Cx‐treated group showed significantly increased mRNA expression of Bcl2 and Oct4 and decreased Caspase3 expression level (p < .05), when compared with the control group. PA‐derived blastocysts from the 40 μM Cx‐treated group also exhibited significantly decreased expression of Bax (p < .05). Our results demonstrated that treatment with 40 μM Cx during IVM improves the developmental competence of PA and SCNT embryos. Improvement of embryo development by Cx is most likely due to increased intracellular GSH synthesis, which reduces ROS levels in oocytes, and it may also positively regulate apoptosis‐ and development‐related genes.