地表覆盖对茶园土壤水分、养分变化及茶树生长的影响

以山东青岛2年生茶园为对象,设置对照(CK)、覆盖秸秆(T1)、覆盖地膜(T2)和覆盖秸秆+地膜( T3 )4个处理,分析了不同覆盖模式对茶园土壤水分和养分以及茶树生长的影响.结果表明:地表覆盖可以保持茶园土壤水分,提高水分利用效率,其中T1、T3处理的茶树生长水分利用效率比CK提高43％ ～48％,产量水分利用效率提高7％ ～ 13％;T1和T3处理土壤有机质、碱解氮、硝态氮、铵态氮的含量显著增加,提高了土壤肥力;叶片硝酸还原酶活性增强,叶片中硝态氮的含量增加,有效地促进茶树生长,茶叶产量比CK增加12％～13％,使茶树新梢生长高峰提前.从茶树生长、茶叶产量、水分和养分利用率、环境安全和经济效益等因素考虑,覆盖秸秆是幼龄茶园地表覆盖的有效方式.     

扎龙湿地不同生境的昆虫多样性

为了探讨湿地不同生境对昆虫物种多样性的影响,对扎龙湿地8种生境的昆虫进行了系统调查.共捕获昆虫5822只,分属11目58科143种,其中直翅目、双翅目、蜻蜒目为扎龙湿地的优势类群.不同生境中,草原草甸昆虫多样性最高,湖边生境多样性指数和均匀度指数均较高,杂草甸均最低.聚类分析和主分量分析结果表明,不同生境的昆虫群落相似性与水资源状况和植被类型有关,捕食性类群种类数和个体数量对昆虫群落稳定性具有重要的调控作用.湖边生境昆虫群落稳定性最强,湿草甸稳定性最弱.湿地水资源状况能影响昆虫生存生境,进而影响昆虫群落的组成和分布格局.     

温度、盐度对强壮箭虫耗氧率和窒息点的影响

研究了不同温度、盐度下强壮箭虫的耗氧率和窒息点.结果表明:温度和盐度均对强壮箭虫的耗氧率和比耗氧率有显著影响.试验温度在5℃-25℃,强壮箭虫个体耗氧率(IO)和比耗氧率(SO)开始随温度的升高而升高,之后呈明显下降趋势.其回归方程分别为y=0.0058x3 -0.2956x2+4.415x-8.7816(R2=0.99,P＜0.05)和y=0.0011x3 -0.0546x2+0.8161x-1.6232(R2=0.99,P＜0.05),数值分别为6.30～11.71μg·ind-1·h-1和1.22 ～2.16μg· mg-1·h-1,窒息点为4.18～6.87 mg·L-1.盐度10 ～40条件下,IO和SO随盐度的升高逐渐下降,回归方程分别为y=-0.0068x2 -0.1412x+21.702(R2=0.89,P＜0.05)和y=-0.0013x2-0.0261x+4.0114( R2 =0.89,P＜0.05),数值分别为4.98～17.73μg ·ind-1·h-1和0.92～3.56 μg·mg-1 ·h-1,窒息点为4.02～6.24 mg·L-1.对强壮箭虫与其他水生动物的耗氧率和窒息点进行比较得出,强壮箭虫是一种狭氧性浮游动物.     

间歇曝气对微污染源水生物接触氧化修复系统脱氮性能的影响

针对寡营养生境下生物脱氮过程碳源不足等问题,开展不同间歇曝气方式对微污染源水生物接触氧化修复系统脱氮性能的影响研究,探究修复系统短程硝化反硝化的可行性与过程机理.结果表明:在停曝-曝气时间为8 h-16 h的间歇曝气方式(Ⅰ)下启动的生物接触氧化修复系统,其铵态氮(NH+4-N)、高锰酸盐指数(CODMn)、总氮(TN)的平均去除率分别稳定在93.0%、78.1%、19.4%;而在停曝-曝气时间为16 h-8 h的间歇曝气方式(Ⅱ)下运行修复系统,其NH+4-N、CODMn平均去除率仍能分别维持在81.2%、76.4%,体系内NO-2-N发生积累,TN去除率增至50%以上.对工况Ⅱ下修复系统周期内氮素转化特性分析发现,在确保出水NH+4-N、溶解氧(DO)浓度达标的前提下,缩短曝气时间可将体系DO长时间控制在0.5～1.5 mg·L-1,亚硝酸氧化菌(NOB)生长及其活性受到抑制,NO-2-N明显累积,最终实现了微污染源水生物接触氧化修复系统的短程生物脱氮.     

Defining the replication program through the chromatin landscape

DNA replication is an essential cell cycle event required for the accurate and timely duplication of the chromosomes. It is essential that the genome is replicated accurately and completely within the confines of S-phase. Failure to completely copy the genome has the potential to result in catastrophic genomic instability. Replication initiates in a coordinated manner from multiple locations, termed origins of replication, distributed across each of the chromosomes. The selection of these origins of replication is a dynamic process responding to both developmental and tissue-specific signals. In this review, we explore the role of the local chromatin environment in regulating the DNA replication program at the level of origin selection and activation. Finally, there is increasing molecular evidence that the DNA replication program itself affects the chromatin landscape, suggesting that DNA replication is critical for both genetic and epigenetic inheritance.     

海拔梯度对长白山北坡岳桦水分利用效率的影响

以分布于长白山北坡海拔1800～2050 m的岳桦林为对象,以叶片碳稳定同位素(δ13C)值作为岳桦长期水分利用效率指示值,探讨海拔梯度对岳桦林水分利用效率的影响.结果表明:随海拔升高,岳桦林土壤体积含水量、比叶质量极显著增加,而叶片含水量和土壤温度显著降低;岳桦叶片δ13C值与海拔呈极显著正相关,增幅为1.013‰·(100 m)-1,与土壤体积含水量、比叶质量呈显著正相关,与生长季土壤平均温度、叶片含水量呈显著负相关.温度不是长白山林线的唯一限制性因子,海拔梯度上水热条件的差异及其交互作用可能造成岳桦生长期间的生理干旱.     

Proteomic profiles of mouse neuro N2a cells infected with variant virulence of rabies viruses

We characterized the proteomes of murine N2a cells following infection with three rabies virus (RV) strains, characterized by distinct virulence phenotypes (i.e., virulent BD06, fixed CVS-11, and attenuated SRV9 strains), and identified 35 changes to protein expression using two-dimensional gel electrophoresis in whole-cell lysates. The annotated functions of these proteins are involved in various cytoskeletal, signal transduction, stress response, and metabolic processes. Specifically, a-enolase, prx-4, vimentin, cytokine-induced apoptosis inhibitor 1 (CIAPIN1) and prx-6 were significantly up-regulated, whereas Trx like-1 and galectin-1 were down-regulated following infection of N2a cells with all three rabies virus strains. However, comparing expressions of all 35 proteins affected between BD06-, CVS-11-, and SRV9-infected cells, specific changes in expression were also observed. The up-regulation of vimentin, CIAPIN1, prx-4, and 14-3-3 theta/delta, and downregulation of NDPK-B and HSP-1 with CVS and SRV9 infection were ≥ 2 times greater than with BD06. Meanwhile, Zfp12 protein, splicing factor, and arginine/serine-rich 1 were unaltered in the cells infected with BD06 and CVS- 11, but were up-regulated in the group infected with SRV9. The proteomic alterations described here may suggest that these changes to protein expression correlate with the rabies virus' adaptability and virulence in N2a cells, and hence provides new clues as to the response of N2a host cells to rabies virus infections, and may also aid in uncovering new pathways in these cells that are involved in rabies infections. Further characterization of the functions of the affected proteins may contribute to our understanding of the mechanisms of RV infection and pathogenesis.