人居环境视角下居民垃圾分类意愿实证研究及政策建议——基于河南省郑州、洛阳、商丘和漯河四地市的调研

基于河南省人居环境现状,分别对郑州、洛阳、商丘和漯河四地市进行了实地调研,通过建立二元Logistic模型,分析了影响居民垃圾分类意愿高低的因素。结果表明:文化程度、经济发展、政策支持对提高居民垃圾分类意愿具有较强的正相关影响,而居民人居环境满意度对提高垃圾分类意愿具有负相关影响;女性相比男性的垃圾分类意愿更高,城市居民相比农村居民的垃圾分类意愿更高。基于此结论,从政府和社会两个方面分别提出了相关建议,以供参考。     

风电开发对坝上地区生态环境的影响研究

在分析坝上地区生态环境现状的基础上,对坝上地区风力发电的优势进行了相关研究,并提出了开发风电的思路。     

论网络环境下图书馆采编人员的素质建设

文献采集是图书馆工作的起点,文献采编人员整体素质的高低直接影响到馆藏文献采集的方针、原则、计划和标准的理解能力和文献采集质量的优劣。论述了网络环境下,采编人员应具备的七大能力,分析了目前采编队伍存在的问题,并探讨了加强采编队伍建设的几项措施。     

卢氏绿壳蛋鸡壳色性状的AY493302标记

卢氏鸡是我国唯一片羽型的可产绿壳蛋的地方鸡种,壳色有绿壳和褐壳2种颜色。本研究采集131只卢氏绿壳蛋鸡,45只卢氏褐壳蛋鸡及18只地方白壳蛋鸡的血液,提取基因组DNA,用微卫星AY493302标记探讨了这3种壳色的基因型差异。结果表明,微卫星AY493302在卢氏绿壳蛋鸡、卢氏褐壳蛋鸡以及地方白壳蛋鸡之间基因型分布差异极显著,基因型AA（225bp/225bp）在卢氏鸡中的频率为0.396 9,且只在卢氏绿壳蛋鸡中出现。其A基因频率在卢氏绿壳蛋鸡、卢氏褐壳蛋鸡和地方白壳蛋鸡中分别为0.698 5,0.500 0,0.500 0。进一步进行测序发现,卢氏绿壳蛋鸡AA基因型在19bp处碱基和217bp处碱基均为G,但卢氏绿壳蛋鸡AB基因型在19bp处碱基却为C,在217bp处碱基与绿壳蛋鸡AA基因型同为G。卢氏褐壳蛋鸡AB基因型和地方白壳蛋鸡的AB基因型则表现在19bp处碱基为C,217bp处碱基为T。AA基因型的序列与NCBI数据库中红色原鸡比较,达99%同源的序列有V00425.1、J02015.1和NW_003763484.1,均位于鸡的1号染色体上。该微卫星标记的群体杂合度、群体多态信息含量在卢氏绿壳蛋鸡中都低于卢氏褐壳蛋鸡和地方白壳蛋鸡。尽管在所研究的卢氏绿壳群体中只有39.7%的个体表现为纯合AA基因型,但卢氏褐壳蛋鸡和地方白壳蛋鸡中没有该基因型,故而认为微卫星AY493302的纯合AA基因型可以作为对卢氏绿壳蛋鸡进行分子标记辅助选择的基因型。     

酸化剂改善动物胃肠道内环境机理的研究

酸化剂可以提高动物的生产性能,改善胃环境,文章从两个方面综述了酸化剂改善动物胃肠道内环境机理的研究,并对酸化剂未来的研究方向做了展望.     

参考群筛选方法及规模对基因型填充准确性的影响

为探究基于A矩阵期望遗传关系最大化（maximizing the expected genetic relationship for matrix A,RELA）、基于A矩阵目标群体遗传方差最小化（minimized the target population genetic variance for matrix A,MCA）、平均亲缘关系最大化（the highest mean kinship coefficients,KIN）、随机选择（random selection,RAN）、共同祖先筛选（common ancestor,CA）等不同参考群筛选方法及参考群规模对基因型填充准确性的影响。本研究使用矮小型黄羽肉鸡作为试验群体,采用鸡600K SNP芯片（Affymetrix Axion HD genotyping array）进行基因分型,测定435羽子代公鸡45、56、70、84、91日龄体重。利用Beagle软件将低密度SNP芯片填充为高密度SNP芯片数据,比较不同参考群筛选方法、参考群规模对基因型填充准确性的影响,以及填充芯片基因组预测准确性。结果表明,使用Beagle 4.0结合系谱信息进行填充效果最佳,其次为Beagle 4.0,而Beagle 5.1填充效果最差。使用MCA方法筛选参考群进行基因型填充准确性最高,使用RAN方法筛选参考群进行基因型填充准确性最低,MCA、RELA、CA 3种方法基因型填充准确性差别较小。相比其他方法,使用MCA方法筛选个体作为参考群将低密度SNP芯片填充至高密度SNP芯片进行基因组选择的预测准确性较高,与真实高密度SNP芯片的基因组预测准确性相差甚微。随着参考群规模增大,基因型填充准确性也随之增加,但增速逐渐下降,最后趋于平缓。综上所述,可以通过参考群筛选方法构建参考群以及控制参考群规模,以保证基因型填充和基因组预测准确性并节省成本,本研究为基因型填充在畜禽遗传育种中的应用提供技术参考。     

皱皮香猪HAS2基因SNPs的鉴定及生物信息学分析

为了探究皱皮香猪全身性皮肤褶皱是否与透明质酸合成酶2（hyaluronan synthase 2,HAS2）基因变异有关,本研究以普通香猪为对照,采用特异性PCR方法克隆HAS2基因的外显子编码区,应用生物信息学方法分析测定基因编码区的碱基变异,检测变异位点在群体中的分布频率。结果显示,皱皮香猪HAS2基因中检测到4个SNPs位点：位于外显子1的T221A错义突变（导致亮氨酸替换为赖氨酸）和A228G同义突变,位于外显子2的T183C和外显子4的C537T同义突变。生物信息学分析发现,T221A和A228G位点构成4种单倍型,其中T-A为皱皮香猪群体的主要单倍型（27.5%）,且在皱皮香猪群体中紧密连锁（r²=0.253）,而且T221A和A228G突变可引起mRNA自由能和蛋白质结构发生变化,TA组合的自由能为-573.29 kJ·mol^-1,TG组合的自由能为-580.89 kJ·mol^-1,AG组合的自由能为-572.66 kJ·mol^-1;AA组合的自由能为-571.03 kJ·mol^-1;蛋白序列中亮氨酸替换为赖氨酸后,α螺旋由35.52%降为32.97%,自由卷曲由43.17%升至44.51%,同时引起蛋白序列三级结构的改变。位点T221A和A228G在香猪群体中呈现出丰富的多态性,均表现出3种基因型;关联分析结果显示,皱皮香猪T221A位点的A等位基因频率显著高于普通香猪（P<0.05）,A228G位点中皱皮香猪的G等位基因频率极显著高于普通香猪（P<0.01）。T183C位点的C等位基因频率和C537T位点的T等位基因频率在皱皮香猪和普通香猪间未达到显著性差异（P>0.05）。研究结果揭示,HAS2基因的外显子1中发生的两个碱基变异可能影响基因转录后mRNA的稳定性以及蛋白的三维结构,影响HA的合成量,并与皱皮香猪体侧皮肤不均匀增厚且发生褶皱有关。     

Identification of the core motif of the BRCA2 C-terminal RAD51-binding domain by comparing canine and human BRCA2

Mammary tumors are the most common tumors in women and non-spayed female dogs. One of the reasons for mammary tumors is mutations of the tumor suppressor gene, BRCA2. BRCA2 participates in homologous recombination repair by interacting with the RAD51 recombinase. BRCA2 has two RAD51-binding domains, consisting of BRC repeats and the C-terminal RAD51-binding domain, respectively. Although several studies have addressed the function of the C-terminal RAD51-binding domain of human BRCA2, the amino acid sequences required for the RAD51-interaction activity remain unclear. In this study, the C-terminal RAD51-binding domains of canine and human BRCA2 were compared; the canine domain displayed a weaker interaction with RAD51. This difference was attributed to the C-terminal portion of the domain via a comparison between canine and human domains. Furthermore, peptides shorter than those previously reported displayed RAD51-interacting activity, and a core motif of this domain consisting of 25 amino acids was identified. Since a mutation (S3323N) was reported in the core motif of this domain, the effect of this mutation was evaluated. The mutant exhibited similar RAD51-binding activity as that of the wild-type protein, suggesting that the mutation was functionally neutral. These data suggested that the C-terminal portion of the BRCA2 C-terminal RAD51-binding domain influenced its RAD51-interaction activity, and a minimum core motif of 25 amino acids was identified in this domain. These data may help clarify BRCA2 function, as well as the tumorigenic effects of BRCA2 mutation.     

Effect of storage duration on egg quality,embryo mortality and hatchability in FUNAAB-ɑ chickens

Effect of extended storage on egg quality, embryo mortality and hatchability in FUNAAB-ɑ chickens was determined. Hatchable eggs (n = 288; weighing 53.2 ± 4.67 g) collected from a flock of FUNAAB-ɑ layer breeder hens aged 32 weeks were stored in egg tray with broad end up under 16 ± 1.5°C for either 0, 4, 8, 12, 16 or 20 d. Before incubation, eight eggs from each group were evaluated for internal and external quality traits. Remaining eggs were set in an incubator and transferred into hatcher on embryonic day 18. Data collected were subjected to one-way analysis of variance. Egg weight loss (EWL; p < .001), surface area (p < .001), yolk diameter (p < .001), inner and outer blastoderm diameters (p < .05) and dead in germ (DIG; p < .001) increased with storage duration while yolk height (p < .001), yolk index (p < .001), albumen weight (p < .05), albumen height (p < .05), albumen index (p < .01), Haugh's unit (HU; p < .05), fertility (p < .001), hatchability of set (HATCHS; p < .001) and fertile eggs (p < .05) decreased. Weight losses of 0, 1.2, 2.2, 3.4, 4.6 and 6.1% were recorded in egg stored for 0, 4, 8, 12, 16 and 20 days respectively. Eggs stored beyond 8 days exhibited higher DIG and lower HATCHS. Shell percentage in 4 days storage (11.4%) was lower (p < .05) than in 16 days storage (13.4%). Shell thickness was similar in eggs stored for 0 to 12 days, but 8 days storage (0.60 mm) had thinner (p < .01) shell than day 16 (0.71 mm) and day 20 (0.73 mm) storage. Internal quality unit (IQU) was higher (p < .05) in fresh eggs (180.4) than in 12 days (167.8) and 20 days (167.8) stored eggs. Extended storage of FUNAAB-ɑ eggs caused EWL, surface area shrinkage, lowered HU and IQU, loss of yolk and albumen quality, increased blastoderm diameters and DIG, and decreased egg fertility and HATCHS from day 8 forward. Storing FUNAAB-ɑ eggs beyond 8 days reduced quality parameters; therefore, other mitigating factors are recommended when storing beyond 8 days.