兰坪坳陷油气组群特征及其成因

兰坪坳陷的油气主要见于金顶矿区的下含矿层，储层主要为上三叠统三合洞组的灰岩和角砾状灰岩。油气地球化学特征表明有机母源输入是多源的，沉积成烃水体介质以还原性占优势．具有较高盐度，有机质热演化处于成熟一高成熟阶段．生物降解改造较为强烈。根据原油的母源贡献、生物降解、环境介质条件等特征，将兰坪坳陷原油划分为3类组群。     

柴达木盆地东部烃源岩的生源与沉积环境

用色谱-质谱、稳定同位素质谱等分析测试技术，对柴达木盆地东部地区寒武系、奥陶系、泥盆系、石炭系和侏罗系岩样进行地球化学特征分析。从饱和烃生物标志化合物特征、正构烷烃单体碳同位素分布特征等方面入手，对该区的烃源岩的生源与沉积环境作了详细研究。结果表明，柴达木盆地东部地区古生界有机质多为菌、藻类生源，少数有陆源有机质混入（主要是石炭系）。有机质多为强还原环境的海相沉积，少数为海陆过渡相沉积。侏罗系在一些地区和层段并非典型的成煤环境，而是属于滨浅湖相，少数为半深湖-深湖环境，因此具有一定的生烃能力。     

鄂尔多斯盆地西峰油田原油地球化学特征及其成因

通过对鄂尔多斯盆地西峰油田原油进行系统地采样和高分辨率的GC-MS、IRMS分析,研究了原油的生物标志化合物和碳同位素组成特征,并且进行了油源对比,探讨了其成因。研究资料指示了所研究原油属于同一成因类型;原油有机母质为菌藻类和高等植物,特别是高等植物为原油的形成作出了贡献;原油形成于弱还原和淡水或微咸水环境;原油均为成熟原油;原油地球化学特征和上三叠统延长组长,油层组具有亲缘关系,反映了原油主要来源于长,油层组。这些研究结果为盆地的石油勘探提供了科学依据。     

中国传统聚落景观区划及景观基因识别要素研究

传统聚落景观区划是一项理论性和实践性都很强的工作,是文化景观区划研究的重要课题之一。基于中国传统聚落景观本身存在的地域性、系统性、稳定性、发展性、一致性、典型性和协调性等特点,本方案以传统聚落景观“意象”(Image) 的内部相似性为前提,以相对一致性原则作为景观区域划分的主导性原则,综合考虑其他原则,如环境制约性原则、文化主导性原则、地域完整性原则、相对一致性原则、面的覆盖性原则、层次性原则和综合性原则等,将全国聚落景观初步划分为3 个大尺度的景观大区、14 个景观区和76 个景观亚区。以往关于文化区的识别,主要从文化特征的角度进行的;关于传统聚落景观区的识别,主要是从景观基因的角度进行的。区域景观基因成为判断传统聚落景观区的核心要素。通常情况下,传统聚落景观基因的判别,可以重点从心理要素、生态要素、美学要素、环境要素、文化要素、时序要素等6 个方面入手。     

基于形态学特征和DNA条形码对中国沿海银口天竺鲷属(Jaydia)分类研究

本研究针对中国沿海银口天竺鲷属鱼类分类鉴定不清晰,同种异名多,种类误鉴等分类问题,结合形态特征比较与DNA条形码技术对其分类鉴定问题进行梳理。2014—2019年间于南海北部沿海采集101尾银口天竺鲷属鱼类标本,经形态学特征鉴定为:横带银口天竺鲷Jaydia striata(Smith & Radcliffe, 1912),特征为体侧有7—11褐色宽横带,腹鳍、臀鳍浅灰色;印度洋银口天竺鲷J.striatodes(Gon,1997),特征为体侧有7—11褐色宽横带,臀鳍后缘黑色;白边银口天竺鲷J.novaeguineae(Valenciennes,1832),特征为臀鳍、尾鳍最下缘为白边;黑边银口天竺鲷J.truncata(Bleeker,1855)特征为第二背鳍、臀鳍中部有一平行基底的黑色带,尾鳍后缘黑色带略宽;史密斯银口天竺鲷J.smithi Kotthaus,1970,特征为第二背鳍中部有一平行基底的黑色纵带,尾鳍后缘黑色带略细;斑鳍银口天竺鲷J.carinatus(Cuvier,1828),特征为第二背鳍最末软条基底有一大黑斑;黑鳃银口天竺鲷J.poeciloptera...     

鄂尔多斯盆地西峰地区延长组烃源岩两环烷烃分布特征及其生源

鄂尔多斯盆地西南部西峰地区三叠系延长组烃源岩检出丰富的两环烷烃,主要为C12~C14和C15、C16两组两环烷烃。其相对丰度表现出3种源岩模式:1以低碳数两环烷烃为主,出现于长71和长81段非烃源岩;2两组两环烷烃都很丰富,出现于长73段富有机质烃源岩;3以高碳数两环烷烃为主,主要发现于长73段烃源岩,也见于长72和长81段。尽管长7段热演化程度基本一致,但补身烷异构化指数变化明显,表明补身烷重排不仅受热演化的影响,而且受有机质来源和沉积环境的控制。延长组烃源岩具有明显的高补身烷优势,反映了烃源岩的还原性沉积环境。烃源岩高丰度C15、C16两环烷烃的检出则指示该地区晚三叠世发育淡水湖泊。葡萄藻不仅是该地区中生界石油的重要母质来源,而且可能是这些两环类标志物的直接生源。     

Identification of five sea cucumber species through PCR-RFLP analysis

Sea cucumbers are traditional marine food and Chinese medicine in Asia. The rapid expansion of sea cucumber market has resulted in various problems, such as commercial fraud and mislabeling. Conventionally, sea cucumber species could be distinguished by their morphological and anatomical characteristics; however, their identification becomes difficult when they are processed. The aim of this study was to develop a new convenient method of identifying and distinguishing sea cucumber species. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis of mitochondrial cytochrome oxidase I gene (COI) was used to identifing five sea cucumber species (Apostichopus japonicus, Cucumaria frondosa, Thelenota ananas, Parastichopus californicus and Actinopyga lecanora). A 692 bp fragment of COI was searched for BamHI, KpnI, PstI, XbaI and Eco31I restriction sites with DNAMAN 6.0, which were then used to PCR-RFLP analysis. These five sea cucumber species can be discriminated from mixed sea cucumbers. The developed PCR-RFLP assay will facilitate the identification of sea cucumbers, making their source tracing and quality controlling feasible.     

Phylogenetic analysis of epibacterial communities on the surfaces of four red macroalgae

Macroalgal surfaces are prone to being attached by bacteria. Epibacterial community structures on marine macroalgae are host-specific but temporally and spatially variable. In this study, we investigated the structure of epibacterial communities on the surfaces of four red macroalgae, Gracilaria lemaneiformis, Gloiopeltis furcata, Mazzaella sp. and Porphyra yezoensis, by analyzing the sequences of 16 S r RNA gene libraries. Healthy individuals of all macroalgae species were collected in winter from a farm at Dalian, China. The results showed that the epibacterial communities were mainly dominated by α-Proteobacteria, γ-Proteobacteria and Bacteroidetes. Deinococcus-Thermus, Spirochaetes and ε-Proteobacteria were also found. The majority of cloned sequences shared the greatest similarity to those of culturable organisms. A large portion of sequences from the α-Proteobacteria homed in Roseobacter clade, i.e., genera Ahrensia, Roseovarius, Litoreibacter, Octadecabacter, Thaiassobacter and Sulfitobacter, while members of Bacteroidetes mainly belonged to family Flavobacteriaceae. The cloned sequences could be separated into 66 OTUs at 0.01 distance value, and rare common OTUs were found among libraries. At genus level, Pseudoalteromonas dominated Gr. lemaneiformis and Gl. furcata libraries, accounting for 72.2% and 47.3%, respectively. Sulfitobacter dominated P. yezoensis library, accounting for 35.4%. A previously undefined cluster within Deinococcus-Thermus dominated Mazzaella sp. library, accounting for 24.6% of the all. These results indicated that a broad range of bacteria inhabited the surfaces of these macroalgae.     

一株H_5N_1亚型禽流感病毒株NA基因的克隆与序列分析

用RT-PCR方法从1个H5N1亚型禽流感病毒分离株A/Chicken/Guangdong/DH/1997扩增NA基因cDNA片段,将其克隆至pMD18-T载体,获得重组质粒pMD-NA,并对其核苷酸序列进行测定和分析。结果表明,该毒株的NA基因长度为1350bp,编码449个氨基酸,与其它H5N1亚型AIV分离株的核苷酸序列同源性为97.0%～99.4%,氨基酸序列同源性为97.7%～99.1%,提示禽流感病毒NA基因保守性较高。NA基因氨基酸序列的聚类分析表明该毒株与来自香港的A/Pheasant/HK/FY155/01和A/Ch/HK/FY150/01两个分离株处于同一进化枝,亲缘关系较近。     

三疣梭子蟹HMGR基因的克隆及其在蜕皮中的表达分析

为了研究3-羟基-3-甲基戊二酰辅酶A还原酶(3-hydroxy-3-methyl glutaryl coenzyme A reductase,HMGR)在甲壳动物蜕皮调控中的作用,采用RT-PCR和c DNA末端快速扩增技术(RACE),克隆得到三疣梭子蟹(Portunus trituberculatus)HMGR基因的c DNA序列(Gen Bank登录号:KF280756)。该序列全长2575bp,包括一个53bp的5′端非编码区,一个686bp的3′端非编码区和一个长度为1836bp的开放阅读框,编码611个氨基酸。该氨基酸序列与已公布的美洲海鳌虾HMGR氨基酸序列相比一致性达65%,具有Ⅰ型HMGR保守催化区域、两个HMG-Co A结合基序和两个NADP(H)结合基序。采用实时荧光定量PCR(q RT-PCR)技术,分析三疣梭子蟹HMGR基因的组织差异表达及在蜕皮周期中的表达水平变化,结果表明HMGR基因在三疣梭子蟹大颚器(MO)中的表达量最高,在其它组织中表达量均极低;在三疣梭子蟹蜕皮周期中,大颚器中HMGR基因的表达量自A期至D0亚期升至最高,然后下降,至D4亚期最低。验证了大颚器是三疣梭子蟹合成甲基法尼酯的唯一器官,表明HMGR在三疣梭子蟹蜕皮调控中起着重要作用。