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。     

罗霄山脉翼手目物种多样性及适生区预测

罗霄山脉位于中国大陆东南部, 是一条南北走向的大型山脉, 面积约6.76万km²。该山脉位于欧亚大陆东部季风区, 生物多样性丰富, 是亚洲东部第三纪冰期动物重要的避难所。为了解罗霄山脉翼手目物种多样性状况, 本研究组于2013-2018年, 使用雾网、手网和竖琴网等工具开展了针对性调查与标本采集, 同时运用形态分类学和分子系统发生学方法鉴定物种。根据调查结果并结合文献记载: 罗霄山脉地区现有翼手目物种4科14属40种, 其中罗霄山脉翼手目新记录种25种, 省级翼手目分布新记录种9种。同时, 本研究基于5年的调查采集位点, 使用生物多样 性与气候变化虚拟实验室(the Biodiversity & Climate Change Virtual Laboratory)在线生境预测平台, 对罗霄山脉翼手目物种当前的适生区, 以及3种不同量温室气体排放情景下(representative concentration pathway, RCP 2.6 / 6.0 / 8.5) 2050年的适生区进行预测, 其中随机森林算法(random forest)的模型解释力较优, 其预测结果显示: 影响该区域翼手目分布的主要环境因子为降水季节性和年平均温度; 山脉中部及南部为翼手目的高适生区, 面积约为罗霄山脉的30%; 与当前适生区相比, RCP 2.6情景下2050年该类群适生区有所扩增, RCP 6.0和RCP 8.5情景下均会导致翼手目适生区急剧缩减, 且分布区将迁移至高海拔区域以响应气候变化。而本项目的开展不仅初步掌握了罗霄山脉翼手目物种多样性本底状况, 也为开展后续的翼手目研究和保护管理提供了参考。     

B para-Bombay phenotype in China caused by homozygous mutation for site 328 G > A of FUT1 gene: a case report

The aim of this paper is to accurately identify a case of B para-Bombay and to analyze the genetic mutation. ABO and Lewis blood groups were identified by standard serological methods, and trace antigens on RBCs were detected by adsorption-elution test, while blood group substances in the saliva were detected by agglutination inhibition test. The ABO gene exons 6-7, FUT1 gene exon 4 and FUT2 gene exon 2 were directly sequenced. Serological results showed that there were B antigens on RBCs without H antigens, anti-A and anti-HI antibodies in serum, and B and H blood group substances in the saliva. The Lewis phenotype was Le (a-b+). According to gene sequencing analysis, ABO, FUT1 and FUT2 genotypes were B101/O02, h^328G/Ah3^28G/A and Se^357C/TSe^357C/T, respectively. This rare phenotype can be mislabeled as "O" if any of the detailed investigations are not performed. Therefore, in order to ensure the safety of blood transfusion, genetic and serological tests are necessary for the correct identification of difficult blood groups.     

“Into and Out of” the Qinghai‐Tibet Plateau and the Himalayas: Centers of origin and diversification across five clades of Eurasian montane and alpine passerine birds

Encompassing some of the major hotspots of biodiversity on Earth, large mountain systems have long held the attention of evolutionary biologists. The region of the Qinghai‐Tibet Plateau (QTP) is considered a biogeographic source for multiple colonization events into adjacent areas including the northern Palearctic. The faunal exchange between the QTP and adjacent regions could thus represent a one‐way street (“out of” the QTP). However, immigration into the QTP region has so far received only little attention, despite its potential to shape faunal and floral communities of the QTP. In this study, we investigated centers of origin and dispersal routes between the QTP, its forested margins and adjacent regions for five clades of alpine and montane birds of the passerine superfamily Passeroidea. We performed an ancestral area reconstruction using BioGeoBEARS and inferred a time‐calibrated backbone phylogeny for 279 taxa of Passeroidea. The oldest endemic species of the QTP was dated to the early Miocene (ca. 20 Ma). Several additional QTP endemics evolved in the mid to late Miocene (12–7 Ma). The inferred centers of origin and diversification for some of our target clades matched the “out of Tibet hypothesis’ or the “out of Himalayas hypothesis” for others they matched the “into Tibet hypothesis.” Three radiations included multiple independent Pleistocene colonization events to regions as distant as the Western Palearctic and the Nearctic. We conclude that faunal exchange between the QTP and adjacent regions was bidirectional through time, and the QTP region has thus harbored both centers of diversification and centers of immigration.     

Integrated Microarray to Identify the Hub miRNAs and Constructed miRNA–mRNA Network in Neuroblastoma Via Bioinformatics Analysis

Neurochemical Research - Neuroblastomas (NB) are childhood malignant tumors originating in the sympathetic nervous system. MicroRNAs (miRNAs) play an essential regulatory role in tumorigenesis and...     

NLRP3 regulates alveolar bone loss in ligature‐induced periodontitis by promoting osteoclastic differentiation

ObjectivesNLRP3 inflammasome is a critical part of the innate immune system and plays an important role in a variety of inflammatory diseases. However, the effects of NLRP3 inflammasome on periodontitis have not been fully studied.Materials and methodsWe used ligature‐induced periodontitis models of NLRP3 knockout mice (NLRP3^KO) and their wildtype (WT) littermates to compare their alveolar bone phenotypes. We further used Lysm‐Cre/Rosa^nTnG mouse to trace the changes of Lysm‐Cre⁺ osteoclast precursors in ligature‐induced periodontitis with or without MCC950 treatment. At last, we explored MCC950 as a potential drug for the treatment of periodontitis in vivo and in vitro.ResultsHere, we showed that the number of osteoclast precursors, osteoclast differentiation and alveolar bone loss were reduced in NLRP3^KO mice compared with WT littermates, by using ligature‐induced periodontitis model. Next, MCC950, a specific inhibitor of the NLRP3 inflammasome, was used to inhibit osteoclast precursors differentiation into osteoclast. Further, we used Lysm‐Cre/Rosa^nTnG mice to demonstrate that MCC950 decreases the number of Lysm‐Cre⁺ osteoclast precursors in ligature‐induced periodontitis. At last, treatment with MCC950 significantly suppressed alveolar bone loss with reduced IL‐1β activation and osteoclast differentiation in ligature‐induced periodontitis.ConclusionOur findings reveal that NLRP3 regulates alveolar bone loss in ligature‐induced periodontitis by promoting osteoclastic differentiation.