民国时期西北地区苜蓿栽培利用刍考

自汉代苜蓿引入我国以来,受到历朝历代的重视,民国时期亦不例外,苜蓿种植利用也得到了发展。在收集近现代有关苜蓿研究文献的基础上,对民国时期西北地区苜蓿种植利用情形进行了梳理与归纳,结果表明,在民国时期西北地区乃为我国苜蓿种植集中区,在陕西、甘肃、新疆、绥远(西部)、宁夏和青海等都有种植,据不完全考查,种植苜蓿的县有52个,其中以陕西最多,达22个县,甘肃次之为14个县,新疆为8个县,绥远(西部)为3个县,宁夏2县(道)和青海1个县。特别是陕甘宁边区发展苜蓿的势头高涨,如1942年边区政府在延安、安塞、甘泉、志丹、定边、靖边等县种植苜蓿达3万亩,陇东种植苜蓿2.3万亩;1944年延川县紫花苜蓿保留面积2.0万亩,到1949年,陕西全省种植苜蓿约98.49万亩。1949年新疆苜蓿保留面积达29300 hm²。绥远河套地区还进行了苜蓿粮草轮作,并建立了苜蓿种植基地。为了鼓励苜蓿种植,边区政府出台了不少政策,例如,1941年边区政府公布了《陕甘宁边区政府建设厅关于种牧草的指示信》,1942年边区政府颁布了《陕甘宁边区卅一年推广苜蓿实施办法》等,李仪祉在治理黄河的方略中,从大农业、生态环境和经济效益出发,提倡广种苜蓿,肥田养畜,并提出了4条种植苜蓿的措施。李烛尘提出,苜蓿根入土深,且能耐旱,适宜西北地区种植和培植草原。苜蓿除用于饲喂家畜外,幼嫩时可当蔬菜食用,在灾荒年也是百姓很好的救荒食物,苜蓿作为农产品常出现在兰州的市场上,试验表明苜蓿保存水土流失的作用要大于作物。     

三江源区土壤侵蚀变化及驱动因素分析

采用修正通用土壤流失方程(revised universal soil loss equation, RUSLE)对三江源区1997-2012年的土壤侵蚀模数和土壤侵蚀量进行定量模拟,并对其生态工程实施前、后时空变化特征进行对比分析,采用空间叠加法分析降雨侵蚀力及植被覆盖度对土壤侵蚀状况的影响,利用模型参数控制法对气候变化和生态工程对土壤侵蚀变化的贡献率进行分析。结果表明:1)生态工程实施后,三江源区土壤侵蚀增加的趋势尚未得到遏制,多年平均年土壤侵蚀模数和侵蚀量较工程实施前增加6.5%,但局部地区土壤侵蚀状况有所好转,约占总面积的45%;2)长江流域在工程实施后的土壤侵蚀量与工程实施前基本持衡;黄河流域土壤侵蚀量增加明显,增幅超过45%;澜沧江流域土壤侵蚀量有所下降,降幅为9.8%;3)降水增强导致土壤侵蚀加剧的贡献率达到180%,植被恢复对土壤侵蚀变化的贡献率为-80%。全面遏制三江源区土壤侵蚀增加趋势,仍需持续努力。     

Heritability and genetic correlations between rumination time and production traits in Holstein dairy cows during different lactation phases

So far, rumination has been used as a proxy for monitoring dairy cow health at farm level. However, investigating its genetic aspects as well as its correlation with other important productive traits may turn this management tool into a new informative selection criterion. However, scientific evidences on genetic correlation among rumination time (RT) and milk production and milk composition are still scarce. Therefore, the objective of this study was to estimate the heritability of RT across three lactation phases and its genetic correlation with milk production, milk composition and somatic cell count (SCC). Results of our study showed that heritability for RT was 0.34 and was constant across lactation. The mean genetic correlations between RT and milk production and composition traits were 0.07 (milk production), ?0.07 (protein yield), ?0.31 (fat yield), and ?0.32 (fat/protein ratio). The mean genetic correlation between RT and the SCC was 0.05.     

Differential gene expression of Eph‐ephrin A1 and LEPR‐LEP with high or low number of embryos in pigs during implantation

The objective of this study was to ascertain whether mRNA and protein expressions of implantation‐related genes (erythropoietin‐producing hepatocellular receptor–ligand A1, Eph‐ephrin A1 and leptin receptor–leptin, LEPR‐LEP) differed between pigs with high and low number of embryos, and whether these differences in gene expression might affect embryo implantation. Experimental pig groups (n = 24) for high and low number of embryos were prepared by altering the number of eggs ovulated in pre‐pubertal gilts treated with 1.5 × (High) or 1.0 × (Low) PG600 ([400 IU PMSG + 200 IU hCG]/dose, AKZO‐NOBEL). Gilts expressing oestrus were artificially inseminated twice and maintained in breeding and gestation until the reproductive tract was collected on day 22 of pregnancy. At slaughter, the reproductive tracts from each pregnant gilt from each treatment were immediately processed to collect samples for RNA and protein analysis. Within each gilt, three conceptus points were sampled, one from each horn and then a random conceptus within the tract. At each conceptus point, endometrial attachment site, chorion–allantois and embryo were collected and immediately frozen in liquid nitrogen. Number of corpus luteum (CL) (35.4 vs. 12.6) and total embryo number (18.8 vs. 10.2) were greater in the high‐embryo compared to the low‐embryo group, respectively (p < .05). Real‐time qPCR results showed that Eph‐ephrin A1 mRNA expression was less in the high‐embryo (p < .05) compared to the low‐embryo group. In addition, Western blotting analysis indicated that Eph‐ephrin A1 and LEP protein expression at endometrial attachment site in high‐embryo was less (p < .05) compared to low‐embryo group. It was also noted that mRNA expression of Eph‐ephrin A1 and LEPR‐LEP was greater in pregnant than non‐pregnant gilts (p < .05). Moreover, mRNA expression of Eph‐ephrin A1 (p < .05) and LEPR‐LEP was greatest at endometrial attachment site among all three tissues. There was a positive correlation between expressions of Eph‐ephrin A1, LEPR‐LEP and embryo length with the correlation coefficient 0.31–0.59. For Eph‐ephrin A1, the highest correlation coefficient appeared between Eph A1 expression and normal embryo number, between ephrin A1 expression and embryo length. For LEPR‐LEP, the highest correlation coefficient appeared between LEPR‐LEP expression and ovary weight (0.79 for both, p < .05), followed by embryo length and weight. The results of this study suggest that low expression of Eph‐ephrin A1 and LEPR‐LEP is somehow related to increased embryo number during implantation and that endometrial attachment site might be the main target tissue of these gene products. Yet, the increased expression of Eph‐ephrin A1 and LEPR‐LEP appeared associated with increased embryo growth (length and weight) and ovary weight, Eph‐ephrin A1 and LEPR‐LEP might play roles in the regulation of embryo implantation in pigs.     

Bovine foetal sex determination—Different DNA extraction and amplification approaches for efficient livestock production

Foetal sex determination using polymerase chain reaction (PCR) in mammals is based on the amplification of gender‐specific foetal DNA sequences circulating in maternal blood. The bovine synepitheliochorial placenta does not allow a direct contact between the trophoblast and the maternal blood, resulting in difficult passage of foetal DNA and, consequently, its very small amounts in maternal bloodstream. Circulating cell‐free foetal DNA (ccffDNA) encompasses short nucleotide fragments (300–600 bp) in maternal circulation. The aim of this study was to assess this non‐invasive method in accurate prenatal sexing in early and late gestational periods in comparison with ultrasound diagnostics. As various DNA isolation and amplification methods were tested, their success in obtaining reliable results was evaluated. Two groups were tested, each consisting of 20 pregnant cows. Blood of a bull and a non‐pregnant heifer was the controls. Extraction of foetal DNA was accomplished by three different methods: using tubes with silicone membranes, a single‐tube extraction without silicone membranes and phenol–chloroform extraction. Following each extraction method, foetal DNA was amplified using PCR and real‐time PCR with both bAML and TSPY primers in a separate reaction. Positive results were obtained only after amplification of foetal DNA extracted with a single‐tube extraction kit. In comparison with ultrasound examination results and foetal gender recorded at birth, the sensitivity of the PCR test was 90% in Group I, but the technique failed to detect male foetuses in Group II. The real‐time PCR test sensitivity in Group I was 90% and in Group II 91.6%.     

Endocannabinoids as endometrial inflammatory markers in lactating Holstein cows

The objective of this study was to consider endocannabinoid system as inflammatory markers in bovine endometrium to better understand the role of this system in regulating many of the functions that are related to inflammatory condition. At day 26 post‐partum, fourteen cows were divided into two groups depending on the inflammatory condition: 1‐ subclinical endometritis (n = 7, with purulent or mucopurulent uterine discharge detectable in the vagina) and 2‐ healthy (n = 7, No (muco)) purulent discharge. Blood samples were collected at 26 and 30 days relative to calving to determine plasma tumour necrosis factor (TNF) and lipopolysaccharide‐binding protein (LBP) concentrations; moreover, uterine biopsy was carried out on day 26 post‐partum to measure mRNA abundance of TNF, interleukin‐1B (IL1B), interleukin‐6 (IL‐6), C‐X‐C motif chemokine ligand 8 (CXCL8), endocannabinoid receptor (CNR2), N‐acyl phosphatidylethanolamine phospholipase D (NAPEPLD), fatty acid amide hydrolase (FAAH), N‐acylethanolamine acid amidase (NAAA) and monoglyceride lipase (MGLL) by real‐time PCR. Results showed mean plasma concentrations of TNF and LBP were lower in healthy cows compared to subclinical endometritis cows (p < .05). Relative mRNA expression for NAAA and FAAH was decreased (p < .05), and relative mRNA expression for CNR2 and NAPEPLD increased in cows with subclinical endometritis compared to healthy cows. In conclusion, relative mRNA expression of TNF, IL1B and CXCL8 and plasma concentration of LBP increased during inflammatory condition along with decreased endocannabinoids hydrolyzing enzyme (NAAA and FAAH), increased enzymes that synthesize endocannabinoids (NAPEPLD) and relative gene expression of the endocannabinoid receptor; together, these contribute to increased endocannabinoids levels during inflammation. Overall, we provide evidence that endocannabinoid system is altered in endometrium tissue during inflammation through increased mRNA expression of CNR2 and synthesis enzyme and decreased mRNA expression of hydrolyzing enzymes interfere with pro‐cytokine production and signalling, which may interfere with the onset and progression of inflammation.     

药剂浸泡种茎对布朗山区木薯地下害虫的防效评价

为了有效防控云南布朗山区木薯重要地下害虫的发生与危害，本试验针对性地开展种茎无害化药剂处理的防效评价研究。结果表明：选用环保型杀虫剂48%乐斯本乳油1 000倍液和1.8%阿维菌素乳油2 000倍液的1∶1混合液浸泡木薯种茎5和10 min后种植效果最好，平均出苗率分别由无任何处理对照的62.5%及清水对照的75.0%和75.6%显著提高到96.5%和97.0%，平均虫害率分别由无任何处理对照的56.8%及清水对照的45.0%和44.8%显著下降到6.3%和5.5%，平均产量分别由无任何处理对照的1 11     

多品种叶面肥水稻田间应用效果探析

[目的]为大面积推广应用多品种叶面肥提供科学依据。[方法]在水稻作物上施用不同品种的叶面肥产品,对比不同叶面肥产品在水稻上的应用效果和经济效益。[结果]在抽穗阶段喷施根外生长调节剂,取得较明显的效果。[结论]根外追肥取得良好的效果,可以继续推广。     

线性红利界下带干扰风险模型的破产概率

考虑到保险公司在实际经营中收益所具有的不确定性和分红策略，建立一类具有线性红利界和带随机扰动的双复合Poisson风险模型，利用鞅方法给出模型关于破产概率的一个定理及上界．     

近32年来新疆地区植被覆盖的时空变化

基于拟合的长时间序列数据监测新疆植被时空动态变化。结果表明,近32年来,新疆植被总体呈现增加趋势,但存在明显的阶段变化和空间差异;植被生长季NDVI值西部和西北部高,东部和东南部低;1982-2013年间新疆植被改善面积大于退化面积,绿洲农田植被覆盖区改善明显、草原区退化严重;整个研究区域的植被重心从北向南移动,天山以北的植被重心呈现西南-东北方向移动,天山以南呈现近似东西方向的移动。