煮熟和干燥处理对黄藤笋抗氧化活性的影响

通过测定黄藤熟笋、生笋(鲜切笋)、熟笋干和生笋干的水和4种不同浓度乙醇提取物中的自由基清除能力、总还原能力、总多酚含量和总黄酮含量,研究了煮熟、干燥加工方法对黄藤笋提取物抗氧化活性的影响。结果表明,煮熟处理能保持或提高提取物的抗氧化活性,干燥处理则相反。乙醇提取物比水提取物具有更高的抗氧化活性,以50%~75%的乙醇提取溶剂效果最好。熟笋在所有溶剂中的自由基清除能力、总还原能力、总多酚含量和总黄酮含量均表现出最高水平,表明煮熟是黄藤笋适宜的加工利用方式。     

中缅边境木材贸易形成和发展的背景

中缅木材贸易主要是双边边境地区之间的木材进出口贸易，是中国历史最为悠久的木材进口贸易之一，有着独特的特征，一直受国际社会广泛关注，却鲜有相关研究。对中缅边境木材贸易形成和发展的深厚背景，包括历史、经济以及社会等进行了深度分析，有助于更加深入地理解中缅边境木材贸易。      

以GIS为基础的禽流感预测预警研究进展

GIS是一种对地理环境等方面数据进行储存、分析、加工和呈现的综合工具。利用GIS可以把流感病例的相关数据与气候、环境和社会等数据进行整合和分析，通过统计学或数学模型，找到影响流感发生和传播的风险因素，对流感的发生趋势进行预测和可视化预警。国内外学者利用GIS在禽流感风险因素分析和预测等方面做了大量研究，包括对人感染H7N9流感、高致病性H5亚型禽流感、野禽流感风险因素和预测的研究，不同基因型病毒分布特征的研究，兽医决策辅助应用研究等。这些研究对指导兽医流行病学研究人员将GIS更好地应用于禽流感防控具有帮助意义。     

棉花蔗糖合成酶基因家族在纤维发育期时空表达模式分析

蔗糖合成酶(Sucrose Synthase)是调控植物糖类代谢的关键酶之一,在植物生长发育及渗透调节过程中起着重要的作用。该酶为多基因家族,各成员在植物不同组织及不同发育阶段发挥不同的作用。陆地棉(Gossypium hirsutum)中有15个Sus成员,本研究利用转录组高通量测序及实时定量PCR技术,检测了该基因家族的表达模式。结果表明,Gh Sus1D、Gh Sus3A、Gh Sus3D和Gh Sus6D在起始期(0~3 DPA)大量表达;GhSus7D在10 DPA的纤维中表达量快速增加,达到同期突变体胚珠的4.7倍;Gh Sus1A、Gh Sus5D在纤维伸长期(5~15 DPA)表达量显著高于胚珠,分别在10 DPA、15 DPA时达到峰值;Gh Sus3A、Gh Sus3D、和Gh Sus6D在纤维发育(15 DPA)时表达量重新上升,且在20 DPA时仍处于较高表达水平。Sus基因家族组织表达模式分析表明,它们在陆地棉品种徐州142野生型和突变体中的组织表达模式基本相同,根、茎、叶、花中没有显著差异。但不同Sus基因具有不同的组织表达特异性。     

不同补水方式下砂壤土渗滤系统对硝态氮去除效果

在水资源短缺的北京地区利用再生水回补城市河湖,一方面对于水资源的可持续利用有着十分重要的作用,另一方面也可能带来地下水环境的潜在污染风险.该文采用100 cm砂壤土柱模拟(河湖岸底)土地渗滤系统,设置定水头淹水、交替淹水落干、定流速补水和侧向补水4种不同再生水回补方式,研究再生水中硝态氮(NO3-N)在土地渗滤系统中的去除效果和迁移转化规律.结果表明,当水力负荷在0.25~2.65 cm/d范围内时,渗滤系统对NO3-N的去除率随着水力负荷的增大而减小;侧向补水方式下渗滤系统对NO3-N的去除效果最优,平均去除率高达96.1%.在定水头淹水和侧向补水方式下,系统对NO3-N的去除主要发生在土柱的上部,而交替淹水落干和定流速补水条件下,土柱中下部对NO3-N也有一定的去除作用.渗滤系统对NO3-N的去除主要取决于系统内部微生物的分布情况,土层中的反硝化细菌数量越大,该土层对NO3-N的去除率就越高.当水温在15~32℃范围内变化时,定水头淹水和交替淹水落干补水方式下,系统对NO3-N的去除率与温度分别呈指数和幂函数关系.该研究表明土地渗滤系统可实现再生水的进一步净化处理,可为再生水安全回补河湖提供参考.     

Development of IP and SCAR markers linked to the yellow seed color gene in Brassica juncea L.

Previous studies showed that the yellow seed color gene of a yellow mustard was located on the A09 chromosome. In this study, the sequences of the molecular markers linked to the yellow seed color gene were analyzed, the gene was primarily mapped to an interval of 23.304 to 29.402M. Twenty genes and eight markers’ sequences in this region were selected to design the IP and SCAR primers. These primers were used to screen a BC₈S₁ population consisting of 1256 individuals. As a result, five IP and five SCAR markers were successfully developed. IP4 and Y1 were located on either side of the yellow seed color gene at a distance of 0.1 and 0.3 cM, respectively. IP1, IP2 and IP3 derived from Bra036827, Bra036828, Bra036829 separately, co-segregated with the target gene. BLAST analysis indicated that the sequences of newly developed markers showed good collinearity with those of the A09 chromosome, and that the target gene might exist between 27.079 and 27.616M. In light of annotations of the genes in this region, only Bra036828 is associated with flavonoid biosynthesis. This gene has high similarity with the TRANSPARENT TESTA6 gene, Bra036828 was hence identified as being the gene possibly responsible for yellow seed color, in our research.     

Effects of Addition of Three Types of Biochar on the Soil Nitrogen Balance and Cotton Yield

The objective of this study was to determine the effect of biochar addition on the soil N balance and cotton yield in a drip-irrigated cotton field. The experiment included four soil amendments: control, cotton straw biochar, corn cob biochar, and poultry manure biochar. The biochar was applied at a rate of 4.5 t·hm^－2 except control. The results showed that all three types of biochar significantly reduced both the apparent soil N loss and the N surplus. The effect of cotton straw biochar treatment was most significant, relative to the control. Plant nitrogen uptake differed significantly between the different treatments, decreasing in the order cotton straw biochar > poultry manure biochar > corn cob biochar. Cotton yield also differed significantly between the different treatments, decreasing in the order poultry manure biochar > corn cob biochar, and cotton straw biochar.     

杨树抗黑斑病相关基因表达谱分析

利用黑斑病的高抗无性系美洲黑杨I-69及黑斑病的高感无性系欧美杨I-45为材料建立的2个cDNA文库,随机挑取cDNA克隆进行5'端EST序列测序,共获得有效序列20 023条.序列经聚类分析和拼接后,共获得10 816个Unigene,其中包括3 734个Contig,7 082个独立的Singleton.被注释的8 853个具有同源性匹配序列基因中,按照GO的分子功能、生物过程和细胞组分3个不同分类角度进行分类.在具有功能注释的8 853个Unigene中,选出330个与完成全基因组测序的毛果杨序列进行BLAST分析,结果发现有177个抗病相关候选基因出现在282个Unigene中,其中135个分布于杨树的18个不同连锁群上,其他42个基因位于还没定位的scaffolds上.所测定的这些EST序列为后期在基因组水平上研究杨树黑斑病的水平抗性遗传机制及进一步的相关基因发现奠定基础.

Abstract：

In an attempt to elucidate the molecular mechanism for resistance of black spot disease in poplar,gene expression profiles in leaves of Populus deltoides'Lus'(I-69/55)and P.euramericana'I-45/51',which were inoculated with the pathogen Marssonina brunnea f.sp.brunnea,were analyzed based on expressed sequence tags (ESTs).A total of 20 023 valid ESTs from the 5'terminal ends derived from corresponding cDNA libraries of the two poplar species were sequenced.Cluster analysis of the 20 023 sequences yielded 10 816 tentative unigenes,including 3 734 contigs and 7 082 singletons.All tentative unigenes were classified by Gene Ontology functional categories.To find resistance-associated candidate genes and locate them on poplar genome,330 unigenes was chosen from 8 853 annotated tentative unigenes,and their BLAST alignment was conducted with Populus trichocarpa assembly,1 77 related candidate resistant genes were found,and they presented in 282 unigenes.Among these genes,there were 1 35 genes located on 18 different linkage groups of poplar genome,and 42 genes located on the different scaffolds.This study supplied a resource of candidate genes for further exploring the genetic mechanism for the host horizontal resistance to the pathogen Marssonina brunnea at the whole genome range,and provided important information for further gene discovery.