四川贡嘎山国家级自然保护区鸟兽多样性

四川贡嘎山国家级自然保护区位于全球生物多样性热点地区之一的横断山区, 是我国生物多样性保护优先区。本文利用红外相机影像和已发表文献对该保护区的大中型兽类和地面活动鸟类进行编目并提出未来监测建议。2011-2018年在97个1 km × 1 km的网格安放红外相机, 累计39,881个相机日, 获得独立有效照片20,932张, 其中野生兽类16,244张, 鸟类2,775张, 牲畜1,737张, 人176张。鉴定出野生兽类30种, 另有文献报道4种和观察3种, 分属于5目15科; 鸟类78种, 分属于9目22科; 牲畜6种。包括12种国家I级和28种国家II级重点保护野生动物; 被CITES附录I收录的有11种, 附录II收录的有12种。被IUCN红色名录评估为濒危(EN)和易危(VU)等级的分别有3种和8种。被《中国脊椎动物红色名录》评估为极危(CR)、濒危和易危等级的分别有5、5和11种。相对多度指数(relative abundance index, RAI)排名前三的兽类是毛冠鹿(Elaphodus cephalophus, 147.39)、水鹿(Rusa unicolor, 66.10)、野猪(Sus scrofa, 36.03); 鸟类是血雉(Ithaginis cruentus, 14.64)、白马鸡(Crossoptilon crossoptilon, 10.43)、大噪鹛(Garrulax maximus, 8.05)。阔叶林、针阔混交林、高山灌丛草甸和高山流石滩是调查薄弱生境, 后期应开展重点调查, 以厘清本区域大中型兽类资源。     

近几十年来冀西北山地白桦次生林径向生长对气候变化的响应

研究不同海拔高度天然次生林径向生长特征及其对气候变化的响应, 揭示影响山地树木径向生长的主要因子, 对于研究气候变化对温带森林生态系统适应性生长、演替和可持续经营的影响具有重要意义。该研究以冀西北山地次生林优势树种白桦(Betula platyphylla)为对象, 于研究区海拔1 350、1 550、1 750、1 950 m处分别设置样地, 采集样木树芯和圆盘, 运用树木年轮气候学方法建立白桦天然次生林标准年表, 并将年轮宽度指数与气候因子进行相关、多元逐步回归分析。主要结果: (1) 1960-2018年研究区气候呈变暖变干趋势, 其中1960-1989年为平稳期, 1989-2018年为快速期。(2)白桦次生林径向生长在1989年发生改变, 年轮宽度指数呈现“增长-下降”的“Λ”形生长趋势。(3)在气候变化平稳期, 白桦次生林径向生长在低海拔样地(B1350、B1550)与气温(平均气温、最高气温、最低气温)呈正相关关系, 在高海拔样地(B1750、B1950)与上年和当年生长季降水量呈显著正相关关系; 在气候变化快速期, 低海拔样地(B1350、B1550)白桦次生林径向生长与生长季气温、生长季潜在蒸散发(ET₀)呈负相关关系, 高海拔样地(B1750、B1950)白桦次生林径向生长与生长季及生长季末期ET₀呈负相关关系。 (4)在气候变化平稳期, 温度对B1350、B1550、B1750样地白桦次生林径向生长的贡献率分别为76%、54%、51%, 水分的贡献率为24%、46%、49%; 在气候变化快速期, 温度对B1350、B1550、B1750样地树木径向生长的贡献率分别为58%、41%、38%, 水分的贡献率为42%、59%、62%; 高海拔B1950样地树木生长始终受水分因子的控制。     

大型煤电基地开发生态累积效应及定量分析方法研究

大型煤电基地(CEBs)是我国煤基能源和材料集中开发区域和国家能源战略安全重要支撑,合理评价CEBs开发生态影响是CEBs可持续协调开发、科学管理中的难点问题。研究将CEBs开发视为系统工程,与自然生态系统(NES)相关联,深入研究大型煤电基地生态系统(CEBES)的驱动行为、内在结构及主要关系、生态影响途径、生态累积过程和生态累积效应及阈值分析方法。基于CEBs空间和功能定位提出CEBs的概念、内涵和特点,融合构建的CEBES涵盖到自然资源、能源开发行为(煤、电等)、其他人类活动(农、牧、城)和大气、水、土壤及生物域;研究表明CEBES的生态累积状态受三种行为驱动和影响(自然行为、能源开发行为和其他人类活动),通过融合、传导和辐射耦合作用,表现为生态要素损伤、系统结构变化和系统状态失衡三级状态,生态累积具有影响多态性、空间多尺度和过程渐变性特点;明确了生态累积过程、累积效应和阈值及其相互关系,引入反映生态影响累积程度的生态损伤系数,提出四类生态阈值(生态要素、内部结构、系统状态和行为调控);基于系统性和实用性筛选反映生态累积相对状态的60项指标,构建具有“三力”驱动、分区要素耦合和系...     

Polyamines Regulate c-Myc Translation through Chk2-dependent HuR Phosphorylation

All mammalian cells depend on polyamines for normal growth and proliferation, but the exact roles of polyamines at the molecular level remain largely unknown. The RNA-binding protein HuR modulates the stability and translation of many target mRNAs. Here, we show that in rat intestinal epithelial cells (IECs), polyamines enhanced HuR association with the 3′-untranslated region of the c-Myc mRNA by increasing HuR phosphorylation by Chk2, in turn promoting c-Myc translation. Depletion of cellular polyamines inhibited Chk2 and reduced the affinity of HuR for c-Myc mRNA; these effects were completely reversed by addition of the polyamine putrescine or by Chk2 overexpression. In cells with high content of cellular polyamines, HuR silencing or Chk2 silencing reduced c-Myc translation and c-Myc expression levels. Our findings demonstrate that polyamines regulate c-Myc translation in IECs through HuR phosphorylation by Chk2 and provide new insight into the molecular functions of cellular polyamines.     

超声激活血卟啉对S180 肿瘤细胞表面EGFR 表达量的影响

目的：探讨超声激活血卟啉处理S180肿瘤细胞后膜表面EGFR表达量的变化。方法：将腹水瘤细胞随机分为四组,U组和UH组细胞分别于频率1．8MHz、2．0W／cm^2的超声装置中照射3min,并分别在1h3h5h后取材,应用免疫组化方法在光镜下观察EGFR的表达情况。结果：1h、3h取材,U组和UH组平均光密度值明显低于Cr组和H组,UH组最低。而5h取材时,UH组平均光密度值显著下降,其它组基本无变化。结论：提示在高频低强度处理下,随着时间的延长,超声激活HpD对EGFR的抑制作用增加,显示可能是基因调控使EGFR表达下调,从而使肿瘤细胞增殖减慢。     

Structural Basis for Non-Covalent Interaction Between Ubiquitin and the Ubiquitin Conjugating Enzyme Variant Human MMS2

Modification of proteins by post-translational covalent attachment of a single, or chain, of ubiquitin molecules serves as a signaling mechanism for a number of regulatory functions in eukaryotic cells. For example, proteins tagged with lysine-63 linked polyubiquitin chains are involved in error-free DNA repair. The catalysis of lysine-63 linked polyubiquitin chains involves the sequential activity of three enzymes (E1, E2, and E3) that ultimately transfer a ubiquitin thiolester intermediate to a protein target. The E2 responsible for catalysis of lysine-63 linked polyubiquitination is a protein heterodimer consisting of a canonical E2 known as Ubc13, and an E2-like protein, or ubiquitin conjugating enzyme variant (UEV), known as Mms2. We have determined the solution structure of the complex formed by human Mms2 and ubiquitin using high resolution, solution state nuclear magnetic resonance (NMR) spectroscopy. The structure of the Mms2–Ub complex provides important insights into the molecular basis underlying the catalysis of lysine-63 linked polyubiquitin chains.     

Genetic differentiation and relationships of populations in the Cycas balansae complex (Cycadaceae) and its conservation implications

BACKGROUND AND AIMS: The Cycas balansae complex is arguably a controversial group with regard to species delineation. Some taxonomists recognize a single polymorphic species while others distinguish five narrowly defined ones. The unresolved taxonomy has the potential to bring about significant problems for species conservation. Thus, an investigation to examine the genetic diversity and differentiation in the C. balansae complex was performed to determine the relationship of populations and to test whether the morphologically defined segregations represent genetically distinct units. METHODS: Inter-simple sequence repeat (ISSR) markers were employed to assess the genetic diversity in the C. balansae complex with a sample of 158 individuals from all extant populations in China. KEY RESULTS: ISSR markers revealed low genetic diversity in all populations studied (H(E) and H(O) averaged 0.0639 and 0.0798 at the population level, respectively). Phenetic analysis showed that the C. balansae complex grouped into five clusters closely corresponding to the narrowly defined C. balansae, C. parvula, C. shiwandashanica, C. tanqingii and C. simplicipinna. CONCLUSIONS: ISSR data suggest that the C. balansae complex has evolved into five genetically distinct units. These might be derived from a relatively widespread common ancestor through multiple vicariant events including geographical isolation resulting from the collision of the Indian plate with the Eurasian plate and from Pleistocene glaciations. In conservation, attention should be paid to each genetic unit.     

The SV40 TC-II(kappa B) enhanson binds ubiquitous and cell type specifically inducible nuclear proteins from lymphoid and non-lymphoid cell lines.

We have characterized the complexes resulting from the specific binding in vitro of proteins present in nuclear extracts of several lymphoid and non-lymphoid cell lines to the TC-I and TC-II sequences of the simian virus 40 (SV40) enhancer. No proteins could be detected, binding selectively to the TC-I sequence, but two proteins TC-IIA and TC-IIB were identified interacting specifically with both the TC-II/kappa B enhanson, 5'-GGAAAGTCCCC-3' (important for the activity of the SV40 enhancer in vivo), and with the related H-2Kb enhanson, 5'-TGGGGATTCCCCA-3'. The binding of these two proteins to mutated TC-II enhansons correlates with the effect of these mutations in vivo, suggesting that both proteins may be important for SV40 enhancer activity. The TC-IIA binding activity was present in nuclear extracts of mature lymphoid B cells and was increased in pre-B cell nuclear extracts by lipopolysaccharide (LPS) and cycloheximide treatment. Furthermore, complex formation between the TC-IIA protein and the TC-II enhanson was efficiently competed by the kappa B motif from the kappa chain enhancer, indicating that TC-IIA is the NF-kappa B factor or a closely related protein. However, in contrast to previous reports, a TC-IIA/NF-kappa B-like protein whose properties could not be distinguished from those of the TC-IIA protein present in lymphoid B cells, was found in nuclear extracts of several untreated non-lymphoid cell lines, notably of HeLa cells, but not of undifferentiated F9 embryonal carcinoma (EC) cells [F9(ND)]. The TC-IIA binding activity which was moderately increased in HeLa cell nuclear extracts by 12-O-tetradecanoylphorbol-13-acetate (TPA) and/or cycloheximide treatment could be induced in nuclear extracts of F9(ND) cells by cycloheximide, but not by TPA. Moreover, the TC-IIA binding activity could be induced in cytosolic fractions from F9(ND) cells by treatment with deoxycholate, indicating that these cells contain an inhibitor protein similar to the previously described NF-kappa B inhibitor, I kappa B. The second TC-II enhanson binding protein, TC-IIB, which could be clearly distinguished from the TC-IIA/NF-kappa B-like protein, by a number of differential properties, resembles the previously described KBF1/H2TF1 protein as it binds with a higher affinity to the H-2Kb enhanson than to the TC-II/kappa B enhanson, and its pattern of methylation interference on the H-2Kb and TC-II/kappa B enhansons is identical to that reported for the KBF1/H2TF1 protein.(ABSTRACT TRUNCATED AT 400 WORDS)     

上海崇明东滩堤内次生人工湿地鸟类冬春季生境选择的因子分析

2004年12月—2005年5月,对上海崇明东滩98海堤内200hm2次生人工湿地进行鸟类调查,在冬季统计到鸟类8目15科56种,以游、涉禽为主;在春季统计到鸟类10目19科55种,以涉禽为主。运用多元回归对鸟类种类数、数量、物种多样性、均匀性指数和科属多样性等群落特征以及调查样点内水位、水面积、植被盖度、底栖动物密度、鱼类捕捞和人类干扰等环境因子进行鸟类生境选择分析。回归模型显示冬季鸟类种类数与植被盖度呈显著正相关,鸟类数量、物种多样性、科属多样性等群落特征与水位高低、水面积比例以及鱼类捕捞强度等有关,底栖动物密度影响鸟类均匀度和数量;春季鸟类数量与鱼塘的水面积呈正相关,而种类和数量与水位呈显著负相关,物种多样性和均匀性明显受水位、水面积和植被盖度影响,鸟类科属多样性与底栖动物密度呈显著相关,捕捞状况对春季鸟类群落影响不大。