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81.
基于卫星高度计的北极海冰厚度变化研究 总被引：5，自引：3，他引：2
A modified algorithm taking into account the first year(FY) and multiyear(MY) ice densities is used to derive a sea ice thickness from freeboard measurements acquired by satellite altimetry ICESat(2003–2008). Estimates agree with various independent in situ measurements within 0.21 m. Both the fall and winter campaigns see a dramatic extent retreat of thicker MY ice that survives at least one summer melting season. There were strong seasonal and interannual variabilities with regard to the mean thickness. Seasonal increases of 0.53 m for FY the ice and 0.29 m for the MY ice between the autumn and the winter ICESat campaigns, roughly 4–5 month separation, were found. Interannually, the significant MY ice thickness declines over the consecutive four ICESat winter campaigns(2005–2008) leads to a pronounced thickness drop of 0.8 m in MY sea ice zones. No clear trend was identified from the averaged thickness of thinner, FY ice that emerges in autumn and winter and melts in summer. Uncertainty estimates for our calculated thickness, caused by the standard deviations of multiple input parameters including freeboard, ice density, snow density, snow depth, show large errors more than 0.5 m in thicker MY ice zones and relatively small standard deviations under 0.5 m elsewhere. Moreover, a sensitivity analysis is implemented to determine the separate impact on the thickness estimate in the dependence of an individual input variable as mentioned above. The results show systematic bias of the estimated ice thickness appears to be mainly caused by the variations of freeboard as well as the ice density whereas the snow density and depth brings about relatively insignificant errors. 相似文献
82.
南大西洋沉积物中多环芳香化合物的组成特征研究 总被引：1，自引：0，他引：1
10 samples of sediments obtained from the South Mid-Atlantic Ridge were measured for the abundances and distributions of polycyclic aromatic compounds(PAHs). The total concentrations of PAHs(∑PAHs) ranged from 2.768 to 9.826 μg/g dry sediment. The ∑PAHs was higher in sample 22V-TVG10 and sample 26V-TVG05 which were close to hydrothermal fields, with the lowest value in sample 22V-TVG14 which was farthest from hydrothermal fields, suggesting a probable hydrothermal origin of ∑PAHs of samples. Approximately nine kinds of PAHs were identified, and low molecular mass tricyclic and tetracyclic aromatic compounds were predominant in the samples. The concentrations of fluoranthene which were typical as hydrothermal alteration compounds were the highest among PAHs with dry weight between 0.913–3.157 μg/g. The phenanthrene homologue was most abundant in the samples, and the ratios between parent phenanthrene and methylphenanthrene which probably reflected the degree of hydrothermal alteration ranged from 0.097 to 1.602. The sample 22V-TVG10 possessing a maximum ratio value showed the intense influence of the hydrothermal alteration on this sample, which might further imply that PAHs in sediments were mainly derived from the hydrothermal alteration. 相似文献
83.
Utilizing Si, Fe and Mn concentrations within the end-member PACMANUS hydrothermal fluid, Si-Fe-MnH_2 O Pourbaix diagrams were constructed at 300°C and 25°C. The Pourbaix diagrams show that the main Si, Fe and Mn oxides species precipitating from the hydrothermal fluid were Si O_2, Fe(OH)_3, Fe_3(OH)_8, Mn_3O_4, and Mn_2O_3 at 25°C. During mixing of hydrothermal fluid with seawater, Si O_2 precipitated earlier than FeMn-oxyhydroxides because of the lower stability boundary. Then Fe(OH)_2 precipitated first, followed by Fe_3(OH)_8 and Fe(OH)_3, and last, small amounts of Mn_3O_4 and Mn_2O_3 precipitated. Fe(OH)_3 was readily deposited in alkaline solution with little influence by Eh. There were many Si-Fe-Mn-concentric particles in the polished sections of the massive precipitates collected from PACMANUS. In the concentric nucleus and ellipsoid, Si oxides precipitated first before the hydrothermal fluid had mixed with seawater. In the concentric nucleus, after the precipitation of Si oxides, the increase of p H and Eh promoted the precipitation of Mn oxides around the Si oxides. In the large ellipsoid, the precipitation of Fe was divided into two periods. In the early period, increase of p H value of hydrothermal fluid produced by low-temperature convection and an input of a small volume of seawater promoted a small amount of Fe(OH)_3 to precipitate in the Si-rich core. In the late period, after complete mixing with seawater and the resultant fluid was close to neutral or slightly alkaline in p H, Fe(OH)_3 was easily precipitated from the solution and distributed around the Si-rich core. 相似文献
84.
中朝-扬子板块碰撞结合带东部边界及海域延伸 总被引：3，自引：0，他引：3
总结了中朝-扬子板块碰撞结合带的边界划分的各类观点,分析了存在争议的原因以及研究的不足之处。通过对苏鲁造山带及黄海海区的重磁资料、周缘断裂特征、典型地震剖面等最新研究成果的收集整理,研究认为华北扬子板块的碰撞结合带应为苏鲁超高压变质带-千里岩隆起,结合带在陆地的北边界可能为五莲-青岛-牟平断裂;南边界为连云港-黄梅断裂;千里岩南缘断裂在印支期是一条千里岩超高压变质带折返的边界断裂,白垩纪以来反转为一条控制南黄海北部坳陷的大型边界断裂,并指出加强黄海海域重磁震资料的精细研究及海陆结合带的构造关系研究是进一步研究重点。 相似文献
85.
Controlled by climate changes, there were three large-scale transgressions and regressions around the Bohai Sea during the late Quaternary, which were accepted by most geologists. However, a big controversy still exists about the time when the transgressions occurred separately. In order to find out the process of the paleoenvironmental changes around the Bohai Sea in the late Quaternary, the foraminifera assemblages from a new borehole Lz908 in the southern coast of the Laizhou Bay were studied, and then the transgressive strata were indentified. Combined with accelerator mass spectrometry radiocarbon 14C（AMS14C） and optically stimulated luminescence（OSL） ages, the occurrence time of these transgressions were re-determined. The result showed that three major large-scale transgressions occurred separately at the beginning of marine isotopic stage 7（MIS7）, the last interglacial period（MIS5） and the Holocene. In addition, a small-scale transgression occurred in the mid-MIS6, and the corresponding transgressive stratum was deposited. The transgressive deposition of MIS3 was also discovered in this study. However, the characteristics of the foraminifera indicated the environment during this period was colder than that in the MIS5. By comparison with the global sea-level changes, the paleoenvironmental changes around the Bohai Sea in the late Quaternary can be consistent with the global climate changes. 相似文献
86.
胶州湾海域面积变化及原因探讨 总被引：2，自引：0，他引：2
基于已有研究成果,利用地形图、海图和遥感影像等资料,提取1863~2012年共6个年代胶州湾海岸线位置,量算5期胶州湾海域面积变化量,制作各期胶州湾海域面积变化及不同开发利用方式面积分布图。研究结果表明:在过去近150 a时间里,胶州湾海域面积减小41%,减小速率最大可达3.71 km2/a;1863年以前,胶州湾海域面积变化完全受自然因素控制;1863~1935年,自然因素是主控因素;1935~2012年,人类活动是主控因素;1863~2012年,填海造陆等开发利用方式导致的胶州湾海域面积变化数量逐期增加。 相似文献
87.
西太平洋深海沉积物古菌多样性垂直分布 总被引：3，自引：2，他引：1
以提取并纯化的西太平洋深海沉积物DNA为模板,利用古菌PCR特异性引物扩增出样品中古菌的16S rDNA片段,构建其克隆文库,建立阳性克隆子RFLP(Restriction Fragment Length Polymor-phism)酶切图谱。据酶切图谱对所获得的120个克隆进行测序,并与数据库中的序列进行比对,从而进行古菌的多样性和系统发育分析。结果表明,沉积物中扩增的16S rDNA古菌序列分别来自泉古生菌(Crenarchaeota)和广古生菌(Euryarchaeota),以Marine Benthic Group B(11.8%)、Marine Benthic Group D(13.6%)、Marine Crenarchaeotic Group(68.69%)为主。少量序列为South African Gold Mine Euryarchaeotic Group(1.07%)、Deep-Sea Hydrothermal Vent Euryarchaeotic Group(1.61%)、UIIB(1.25%)、VALIII(1.79%)、Marine Benthic Group E(0.18%)。以上结果表明西太平洋深海沉积物中有丰富多样的古菌群落。 相似文献
88.
为了研究西太平洋黑潮源区不同深度沉积物中古菌群落结构的多样性,应用16S rDNA文库技术,对IMAGES XIV航次采集的岩芯MD06-3047进行基因文库的构建和分析,得到260个克隆,经分析处理后得到56个OTUs(Operational Taxonomic Units).基于16S rRNA序列的同源性比较,绘制系统进化树,进行统计学分析.研究结果显示,西太平洋黑潮源区的本哈姆高原(Benham Rise)沉积物中有丰富多样的古菌群落,在1m内的沉积物中分布着9种古菌类群.古菌序列归属于泉古菌(Crenarchaeota)和广古菌(Euryarchaeota),并以泉古菌为主(占总序列的91.5％).其中,泉古菌包含MGI、MBG-B、MCG和UCII-b 4个类群,并且主要由MGI构成(占总序列的40.8％),而广古菌包含MBG-D、SAGMEG、DHVEG、MBG-E和VAL Ⅲ 5个类群,各类群所占总序列比例均较低(占总序列的0.4％～5.4％之间).研究结果对于理解西太平洋黑潮源区沉积物中古菌多样性有重要意义,并为今后研究古菌群落与环境之间的关系提供科学依据. 相似文献
89.
90.
根据2010年4—5月国家基金委南海多学科综合航次在南海中部和北部的调查资料,利用抽真空气相色谱法测定海水中溶存甲烷浓度,分析了该海区上层海水中溶存甲烷的浓度、饱和度及海气交换通量。南海中部和北部表层海水中溶存甲烷浓度范围为1.15—5.6nmol·L?1,平均值为2.2nmol·L?1,饱和度范围为59.7%—298.8%,59%站位的溶存甲烷处于过饱和状态。甲烷海气交换通量范围分别为?17.7—61.3μmol·m?2·d?1(根据 LM-86方程计算)和?27.9—119.6μmol·m?2·d?1(根据 W-92方程计算)。南海是大气中甲烷的来源之一,年甲烷辐射量估算值为2.7×10?2—4.0×10?2Tg·a?1。 相似文献