2004-2013年珠江流域植被变化及其胁迫分析

植被对区域气候调节、水文循环等有着重要作用,在近年来中国南部地区极端气候频发的背景下,研究植被变化及胁迫意义重大。以珠江流域为研究区,利用MODIS EVI分析了植被的变化规律,并通过美国军事气象卫星DMSP灯光数据和气象数据探讨分析了人类活动和自然环境对植被变化的胁迫。结果显示：2004年到2013年期间珠江流域内年平均EVI介于0.33-0.38之间,EVI从高到底依次是常绿阔叶林 > 混交林 > 多树的草地 > 常绿针叶林 > 草地,不同植被类型的EVI变化趋势基本一致,同一植被类型EVI年际变化较小,其中混交林和草地年际最大变化量分别为0.07和0.04,而常绿阔叶林、常绿针叶林和多树的草地年际最大变化量均为0.06;在2004年至2013年年间,城市化水平增长了约71%,其年发展变化与EVI的年变化趋势相反;通过对比分析发现珠江流域人类活动对植被变化影响高于自然环境,即DMSP灯光变化与EVI变化的相关系数明显高于气温和降水。     

山西高原草地景观的数量分类与排序

草地植被空间格局研究是草地景观研究中一项重要的基础工作。空间格局研究不仅限于描述景观的空间特征,而是要深入分析空间格局的分布规律及影响格局形成的原因及机制。以1∶50万《山西省草地类型图》、《山西省行政区域图》及《山西省地形图》为主要信息源,借助GIS技术,应用TWINSPAN和DCA对山西高原草地景观的1127个样方进行研究。结果表明:(1)在TWINSPAN分类结果中,31个群丛组从左到右的排列顺序很好地揭示了山西高原草地景观的纬向地带性分布规律。即从40°43'N向34°34'N依次分布着北部草原、中部灌草丛和草丛及南部的暖温带草丛。(2)1127个样方DCA排序图纵轴揭示了明显的海拔梯度,即由上至下海拔逐渐降低,相应地草地景观变化为亚高山草甸、灌草丛、草原及河漫滩草甸;DCA排序图的横轴揭示了明显的水分梯度,即从左到右水分逐渐增加。两大优势群丛组样方及44个优势群丛组物种DCA的排序图都很好地刻画了山西高原水热组合的变化,即从西北向东南由于地形地貌引起的水热组合由冷干向暖湿逐渐变化,水热组合的梯度变化进一步影响了草地景观整体的空间分布格局。(3)GIS技术与数量生态学方法相结合有助于丰富景观生态学研究的技术体系。     

北京城区人工构筑物对比邻绿地土壤温度和含水量的影响

选取城市中分布最广的两类人工构筑物——沥青和混凝土为研究对象,采用构筑物-绿地梯度样带法,观测这2类典型城市构筑物对比邻绿地土壤温度和含水量的影响,分析不同构筑物的质地、面积、形态等构筑物特征对土壤水、热分布的影响强度及范围。研究显示:1)夏、秋季在构筑物-绿地梯度样带上,绿地土壤温度在比邻构筑物端(a点)处最高,并且白天中午、傍晚时段a点温度显著高于梯度上其他观测点和对照点;2)绿地土壤含水量在比邻构筑物端(a点)处最低,而且土壤含水量变化在梯度样带上从a点至远离构筑物端的对照点变化具有不确定性,可能受城区土壤蒸散、人工灌溉、土壤地下生物量等不确定因素的影响。3)梯度样带上土壤温度(T)和水分(W)与离a点距离(D)均呈现幂函数定量关系,即沥青样地T=0.7708(579.4957-0.9984D)0.5843,W=0.1970(0.0505+0.1347D)0.2262;混凝土样地T=0.7615(583.7027-1.0986D)0.5746,W=0.2224(-0.6019+0.3473D)0.0595。4)在构筑物-绿地梯度样带上,土壤温度和含水量受构筑物影响幅度大概在0—100 cm之间,而且随构筑物质地及分布格局、城市气象以及绿地构成、结构、人工管理方式等因素的影响而变化。     

采伐干扰对华北落叶松细根生物量空间异质性的影响

以华北落叶松天然林为研究对象,选择采伐干扰林分(样地A)和未采伐干扰林分(样地B),利用根钻法分3层(0—10cm,10—20cm,20—30cm)获取各径级细根(≤1mm、1—2mm、2—5mm3级活细根,≤2mm死亡细根)生物量数据。采用地统计学变异函数和经典统计相结合的数据分析方法对采伐干扰造成的细根生物量空间异质性的变化进行定量研究。主要研究结果如下:采伐干扰林分样地A各经级细根生物量均值减少;同一土层相同径级细根生物量样地A与样地B相比差异显著(P<0.05);不同土层的细根生物量异质性具有显著差别(P<0.05)。0—10cm土层,未采伐干扰林分≤1mm细根生物量呈现较明显的空间自相关变异,采伐干扰林分则表现为随机性变异特征,采伐干扰导致≤1mm细根生物量空间分布特征更加复杂(分维数D=1.978);10—20cm土层,采伐干扰林分各径级细根生物量异质性程度明显降低,只有未采伐干扰林分的5.4%—88.9%。20—30cm土层,未采伐干扰林分≤1mm细根生物量在较小尺度范围(<2.9m)表现出明显的空间自相关变异(结构方差比86.1%),受采伐干扰林分各径级细根生物量异质性程度只有未采伐干扰林分的8.9%—45.9%,且呈现随机性变异。各径级细根生物量空间异质性的垂直分异均表现为随土层深度的增加异质性强度明显降低。     

石家庄西部太行山区景观格局时空变化

基于1987、2000年两期TM、ETM＋遥感数据资料,利用ArcGIS提取石家庄西部太行山区的景观类型转移矩阵,并结合重心模型,从时间和空间上对景观格局动态变化进行分析。结果表明：（1）1987～2000年,景观基质均为耕地,林地、草地、水域、建设用地和未利用土地作为斑块单元镶嵌其中;耕地、草地和水域的面积均为减少,其中草地面积减少量最大,主要向林地转化;林地、建设用地和未利用土地的面积均为增加,其中建设用地面积增加量最大,主要由未利用土地转化而来。（2）1987～2000年间,水域重心迁移距离最大;耕地、水域和建设用地的重心偏移方向为北偏西;林地和草地的重心偏移方向为北偏东;未利用土地的重心偏移方向为南偏西。     

Comprehensive peptidome analysis of mouse livers by size exclusion chromatography prefractionation and nanoLC-MS/MS identification

Peptidome analysis has received increasing attention in recent years. Cancer diagnosis by serum peptidome has also been reported by peptides' profiling for discovery of peptide biomarkers. Tissue, which may have a higher biomarker concentration than blood, has not been investigated extensively by means of peptidome analysis. Here, a method for the peptidome analysis of mouse liver was developed by the combination of size exclusion chromatography (SEC) prefractionation with nano-liquid chromatography-tamdem mass spectrometry (nanoLC-MS/MS) analysis. The extracted peptides from mouse liver were separated according to their molecular weight using a size exclusion column. MALDI-TOF MS was used to characterize the molecular weight distribution of the peptides in fractions eluted from the SEC column. The low molecular weight (LMW) (MW < 3000 Da) peptides in the collected fractions were directly analyzed by LC-MS/MS which resulted in the identification of 1181 unique peptides (from 371 proteins). The high molecular weight (HMW) (MW > 3000 Da) peptides in the early two fractions from the SEC column were first digested with trypsin, and the resulted digests were then analyzed by LC-MS/MS, which led to the identification of 123 and 127 progenitor proteins of the HMW peptides in fractions 1 and 2, respectively. Analysis of the peptides' cleavage sites showed that the peptides are cleaved in regulation, which may reflect the protease activity and distribution in body, and also represent the biological state of the tissue and provide a fresh source for biomarker discovery.     

黄芪对镉致大鼠睾丸支持细胞超微结构及波形蛋白、E-钙粘蛋白表达改变的保护作用

目的 探讨黄芪对镉致大鼠睾丸支持细胞损伤的保护作用.方法 21只成年雄性SD大鼠随机分成镉组(0.1％氯化镉腹腔内注射,1mg/Kg体重/天,5天/周,处理后1、2、3、4周取材)、镉加黄芪组(注射氯化镉的同时注射黄芪,10g/Kg体重/天,5天/周,处理后2、4周取材)和对照组(腹腔内注射等量生理盐水).睾丸取材作光镜、免疫组织化学染色和图像分析及超微结构观察.结果 光镜H.E染色对照组支持细胞核不规则,染色浅,核仁明显,镉处理后胞浆内有空泡形成,镉加黄芪组支持细胞未见明显改变.对照组波形蛋白阳性产物在支持细胞靠近基室腔的胞浆中表达,E-钙粘蛋白阳性产物则主要定位于生精上皮近腔室的支持细胞和部分生精细胞胞浆中.镉处理后支持细胞胞浆中波形蛋白和E-钙粘蛋白阳性产物表达的平均光密度值均明显降低(P＜0.05),镉加黄芪组阳性产物表达虽较对照组减弱但明显高于相应镉组(P＜0.05).镉处理组支持细胞胞质特化区和紧密连接破坏,镉加黄芪组支持细胞超微病变较相应镉组为轻.结论 镉降低大鼠睾丸支持细胞波形蛋白和E-钙粘蛋白的表达并造成支持细胞的超微结构损伤,黄芪具有较好的保护效果.     

Astragalus saponin attenuates the expression of fibrosis-related molecules in irradiated cardiac fibroblasts

The main pathological change of radiationinduced heart disease is fibrosis. Emerging evidence has indicated that Astragalus membranaceus and its extractant, Astragalus saponin （AST）, were used for treating fibrosis diseases. In the present study, the effects of AST on fibrosis damage induced by irradiation were determined. After being irra diated with 1 or 2Gy Xrays, obvious changes of endoplas mic reticulum morphology were observed in cardiac fibroblasts （CFs）, suggesting that its protein processing function was imbalanced, which indirectly indicated that fi brosis damage was caused by irradiating CFs. The expres sion levels of TGFfll and collagen I （Coll） were increased at 48h postirradiation. Administration of 20 μg/ml AST reduced the production of reactive oxygen species in irra diated CFs and decreased the expression of Coll, TGFfll, and pSmad2/3. Polymerase chain reaction （PCR）array analysis showed that there were -30 genes which were mainly classified into extracellular matrix, remodeling enzymes, inflammatory cytokines/ehemokines, and TGF superfamily, were upregulated after treatment with 1Gy Xray, whereas most of these genes were downregulated when pretreated with 20 μg/ml of AST. In addition, TIMP1 and Smad7 genes that were downregulated after treatment with 1Gy Xray were upregulated when pretreated with 20 μg/ml of AST. In conclusion, radiationinduced fibrosis damage was observed at a cellular level. AST attenuated this fibrosis damage effect in irradiated CFs and this anti fibrosis effect may be closely related to its antioxidant action. The involvement of fibrosisrelated molecules in irradiated CFs was systematically demonstrated by a PCR array for the first time. AST reversed the expression of the majority of genes changed by irradiation, which further confirmed its antifibrosis effect.     

Extracellular vesicle RNAs reflect placenta dysfunction and are a biomarker source for preterm labour

Preterm birth (PTB) can lead to lifelong complications and challenges. Identifying and monitoring molecular signals in easily accessible biological samples that can diagnose or predict the risk of preterm labour (PTL) in pregnant women will reduce or prevent PTBs. A number of studies identified putative biomarkers for PTL including protein, miRNA and hormones from various body fluids. However, biomarkers identified from these studies usually lack consistency and reproducibility. Extracellular vesicles (EVs) in circulation have gained significant interest in recent years as these vesicles may be involved in cell‐cell communication. We have used an improved small RNA library construction protocol and a newly developed size exclusion chromatography (SEC)‐based EV purification method to gain a comprehensive view of circulating RNA in plasma and its distribution by analysing RNAs in whole plasma and EV‐associated and EV‐depleted plasma. We identified a number of miRNAs in EVs that can be used as biomarkers for PTL, and these miRNAs may reflect the pathological changes of the placenta during the development of PTL. To our knowledge, this is the first study to report a comprehensive picture of circulating RNA, including RNA in whole plasma, EV and EV‐depleted plasma, in PTL and reveal the usefulness of EV‐associated RNAs in disease diagnosis.