基于无人机低空遥感的荒漠植被覆盖度与归一化植被指数验证及其对水热梯度的响应

为了验证在荒漠地区MODIS-NDVI产品的精度以及为在气候变化背景下荒漠草地的科学管理提供依据,本文利用无人机低空遥感研究了干旱荒漠地区植被覆盖度(FVC)和归一化植被指数(NDVI)对水、热梯度的响应规律。在内蒙古阿拉善荒漠地区的100个样点采用GreenSeeker手持光谱仪获得NDVI值(NDVI_R),通过MODIS-NDVI数据产品提取每个样点的NDVI(NDVI_M),借助NDVI_R验证NDVI_M的精确度;通过无人机遥感手段获得每个采样点的FVC(FVC_U),利用像元二分模型反演每个样点的FVC(FVC_M),借助FVC_U验证FVC_M的精确度;并结合气象数据探讨基于无人机低空遥感的荒漠地区FVC和NDVI对水热梯度的响应。结果表明: MODIS-NDVI数据产品能够反映阿拉善地区的NDVI,精确度为84.2%,但比真实值高15.7%;FVC_M能够反映阿拉善地区的FVC状况,精确度为83.1%,但比真实值低14.8%;不同采集方式获得的NDVI受气象因子的影响程度不同,NDVI不仅受气温和降雨的影响,也受地温、蒸发量以及两者相互作用的影响,由于受大气影响程度不同, NDVI_M受地温、蒸发量、降水量的影响比NDVI_R大,NDVI_R受气温的影响比NDVI_M大。在阿拉善地区研究FVC随水热梯度的变化不仅要考虑降水量和气温,还应考虑蒸发量、地温以及气象因子之间相互作用的影响,其中,气温与降雨、蒸发量与地温以及气温与蒸发量之间相互作用对FVC_U的影响较大。     

中亚热带典型人工林土壤酶活性及其化学计量特征

以中亚热带典型的马尾松林、湿地松林和马尾松-木荷混交林(针阔混交林)为研究对象,分析不同林分类型下0～10和10～20 cm土层的β-D-葡萄糖苷酶(BG)、β-N-乙酰氨基葡萄糖苷酶(NAG)、亮氨酸氨基肽酶(LAP)、酸性磷酸酶(AP)、多酚氧化酶(POX)、过氧化物酶(POD)6种土壤酶活性,以及酶化学计量比及土壤理化性质特征,分析驱动中亚热带典型林分类型土壤酶活性及其计量比变异的主要因素。结果表明: 林分类型显著影响了土壤BG和LAP活性,表现为湿地松林10～20 cm土层土壤BG显著高于马尾松林,而LAP在马尾松林最高;湿地松林10～20 cm土层土壤BG/(NAG+LAP)、BG/AP显著高于马尾松林,而马尾松林(NAG+LAP)/AP显著高于湿地松林和针阔混交林;林分类型间酶化学计量的向量长度在10～20 cm土层差异显著,表现为湿地松林>针阔混交林>马尾松林。3种人工林酶化学计量的向量角度均大于45°,其中在湿地松林10～20 cm土层向量角度显著大于马尾松林。冗余分析表明,土壤碳质量指数和有机碳与全磷的比值(C/P)以及土壤含水量和C/P分别是0～10和10～20 cm土层土壤酶活性及其化学计量的关键影响因素,土壤碳和磷的数量和质量,以及土壤含水量在调节中亚热带人工林生态系统养分循环中发挥关键作用。     

复方泛影葡胺速率区带密度梯度离心法纯化衣原体

目的利用速率区带密度梯度离心法建立纯化高纯度、高感染力衣原体的方法。方法采用HeLa229细胞扩增衣原体,制作含有大量衣原体的细胞裂解液,以国产复方泛影葡胺作为介质,利用速率区带密度梯度离心法纯化衣原体,负染纯化产物后使用透射电镜观察形态,并将纯化产物感染HeLa229细胞,测定纯化产物的感染力。结果在透射电镜下观察,证实纯化产物为直径300 nm左右的高纯度原体。纯化产物的感染力为8.62×10~8 IFU/mL,证实该纯化产物具有高感染力。结论通过复方泛影葡胺速率区带密度梯度离心法,可获得高纯度、高感染力的衣原体,为开展衣原体感染机制、免疫反应等研究提供了有效而可靠的保证。     

6-gingerol protects nucleus pulposus-derived mesenchymal stem cells from oxidative injury by activating autophagy

BACKGROUNDTo date, there has been no effective treatment for intervertebral disc degeneration (IDD). Nucleus pulposus-derived mesenchymal stem cells (NPMSCs) showed encouraging results in IDD treatment, but the overexpression of reactive oxygen species (ROS) impaired the endogenous repair abilities of NPMSCs. 6-gingerol (6-GIN) is an antioxidant and anti-inflammatory reagent that might protect NPMSCs from injury.AIMTo investigate the effect of 6-GIN on NPMSCs under oxidative conditions and the potential mechanism.METHODSThe cholecystokinin-8 assay was used to evaluate the cytotoxicity of hydrogen peroxide and the protective effects of 6-GIN. ROS levels were measured by 2´7´-dichlorofluorescin diacetate analysis. Matrix metalloproteinase (MMP) was detected by the tetraethylbenzimidazolylcarbocyanine iodide assay. TUNEL assay and Annexin V/PI double-staining were used to determine the apoptosis rate. Additionally, autophagy-related proteins (Beclin-1, LC-3, and p62), apoptosis-associated proteins (Bcl-2, Bax, and caspase-3), and PI3K/Akt signaling pathway-related proteins (PI3K and Akt) were evaluated by Western blot analysis. Autophagosomes were detected by transmission electron microscopy in NPMSCs. LC-3 was also detected by immunofluorescence. The mRNA expression of collagen II and aggrecan was evaluated by real-time polymerase chain reaction (RT-PCR), and the changes in collagen II and MMP-13 expression were verified through an immunofluorescence assay.RESULTS6-GIN exhibited protective effects against hydrogen peroxide-induced injury in NPMSCs, decreased hydrogen peroxide-induced intracellular ROS levels, and inhibited cell apoptosis. 6-GIN could increase Bcl-2 expression and decrease Bax and caspase-3 expression. The MMP, Annexin V-FITC/PI flow cytometry and TUNEL assay results further confirmed that 6-GIN treatment significantly inhibited NPMSC apoptosis induced by hydrogen peroxide. 6-GIN treatment promoted extracellular matrix (ECM) expression by reducing the oxidative stress injury-induced increase in MMP-13 expression. 6-GIN activated autophagy by increasing the expression of autophagy-related markers (Beclin-1 and LC-3) and decreasing the expression of p62. Autophagosomes were visualized by transmission electron microscopy. Pretreatment with 3-MA and BAF further confirmed that 6-GIN-mediated stimulation of autophagy did not reduce autophagosome turnover but increased autophagic flux. The PI3K/Akt pathway was also found to be activated by 6-GIN. 6-GIN inhibited NPMSC apoptosis and ECM degeneration, in which autophagy and the PI3K/Akt pathway were involved.CONCLUSION6-GIN efficiently decreases ROS levels, attenuates hydrogen peroxide-induced NPMSCs apoptosis, and protects the ECM from degeneration. 6-GIN is a promising candidate for treating IDD.     

Mycorrhizal type governs foliar and root multi-elemental stoichiometries of trees mainly via root traits

Plant and Soil - Multi-elemental stoichiometry can represent the biogeochemical niches of species, which can further guide community assemblage. Mycorrhizae play a key role in plant elemental...     

Multivariate analysis of volatile profiles in tea plant infested by tea green leafhopper Empoasca onukii Matsuda

Plant Growth Regulation - The tea green leafhopper (Empoasca onukii Matsuda) is a severe pest for the tea plant (Camellia sinensis (L.) O. Ktze), which significantly reduces the tea yields and...     

An in-depth analysis reveals two new genetic variants on 22q11.2 associated with vitiligo in the Chinese Han population

Molecular Biology Reports - Vitiligo is a complex disease in which patchy depigmentation is the result of an autoimmune-induced loss of melanocytes in affected regions. On the basis of a...