中祁连东段什川杂岩基的岩石化学特征及年代学研究

祁连造山带被托菜南山-了高山构造带及宗务隆山-贵得构造带分为北祁连、中祁连及南祁连构造带。什川岩基位于中祁连构造带东部,由闪长岩、斜长花岗岩、二长花岗岩组成;对二长花岗岩进行U-Pb单颗粒锆石微区LA-ICP-MS同位素测定,获得444.6Ma及414.3Ma两组加权平均年龄,前者代表岩石的形成年龄,后者代表构造热事件年龄。二长花岗岩主量元素W(SiO_2)=68.66%～80.77%,w(K_2O)/w(Na_2O)>1和A/CNK介于0.95～1.21间,总体为钾质钙碱性过铝质花岗岩。岩石富集LILE元素(K、Th、Rb、Ba等),亏损HFSE元素(Ta、Nb、Y等);稀土元素总量较高(∑REE多介于109.05×10~(-6)～322.66×10~(-6)),轻重稀土强烈分馏(∑LREE/∑HREE介于7.92～31.68),稀土元素分配模式为轻稀土富集型,具中等-强Eu负异常(δEu=0.26～0.58)。岩石矿物组合及岩石地球化学特征共同表明,什川岩基为中上地壳泥砂质岩石部分熔融而成,形成温度较低,为加厚地壳拆沉熔融成因。这为祁连造山带构造演化及其深部动力学机制研究提供了新的资料。     

滇西点苍山—哀牢山变质岩系锆石SHRIMP定年及其地质意义

滇西点苍山和哀牢山主体分别由下元古界苍山群和哀牢山群深变质岩系组成,被认为是前寒武纪结晶基底。选取点苍山的花岗闪长质糜棱岩(DCS-1)和哀牢山元江段黑云母花岗闪长质片麻岩(SM07-1)之中的锆石进行U-Pb SHRIMP定年。样品DCS-1和SM07-1测年结果分别为233±2.6Ma和239.8±2.8Ma。结合前人对滇西地区花岗质岩类所做的研究,揭示滇西地区在三叠纪经历一期在空间上广泛分布的岩浆事件,点苍山花岗质糜棱岩和哀牢山花岗质片麻岩的原岩为三叠纪侵位的花岗岩,其构造环境属于大陆裂谷,反映了滇西地区在三叠纪地壳物质的重新调整,而该变质岩系不是前寒武纪的结晶基底,其变质作用与山体出露地表过程和新生代构造作用有关。     

西藏普兰地区拉昂错蛇绿岩中辉绿岩的锆石SHRIMP U—Pb年龄及其地质意义

蛇绿岩中的辉绿岩岩墙是洋脊扩张的产物．其形成年龄代表了扩张事件的时间,也代表了蛇绿岩的形成时代？对雅鲁藏布江缝合带西段拉昂错蛇绿岩中的辉绿岩岩墙进行锆石SHRIMPU—Pb定年,得出加权平均年龄为120．2Ma±2．3Ma,代表辉绿岩的结晶年龄。结合已有的关于雅鲁藏布江蛇绿岩的形成年龄（西段休古嘎布122．3Ma±2．4Ma,中段大竹卡126．0Ma±1．5Ma、吉定123．0Ma＋_1．8Ma,东段罗布莎162．9Ma±2．8Ma）的报道,表明拉昂错地区特提斯洋海底扩张的时代与体古嘎布地区一致．雅鲁藏布江西段与中段地区洋盆的形成时代一致,但晚于东段的发育时代。这意味着整个东提斯洋盆的发育时代存在东早西晚的特点。     

用铀系定年法测定南永1井珊瑚礁年龄

运用铀系定年法首次对南水1井珊瑚礁岩心中的两个层位进行测年,结果与~(14)C测年一致,证实在晚更新世与全新世之间存在沉积间断面。     

海洋沉积样品~(14)C测年差异来源及其结果解释

~(14)C测年已为海洋研究工作广泛应用,但由于时有不合理取样或在运用数据时没有充分考虑各种海洋环境和动力因素,因而产生无法使用数据作合理解释的现象。本文试从海洋样品本身和海洋各种营力作用分析各种数据差异的来源,认为海洋环境特别是海岸带环境的复杂性是造成海洋样品~(14)C测年数据差异的主要原因,它可能影响样品的代表性或使数据解释时得出错误结论.并指出在运用年代结果时一定要充分考虑地质地理和各种营力作用因素。     

牙鲆种群动态及其资源管理

本文根据1980—1986年间鱼类生物学参数测定,结合体长分布资料的模拟分析,研究黄、渤海区牙鲆种群年龄结构、死亡动态以及在不同年龄和死亡率条件下世代资源生物量变化的规律。模型分析结果表明,当F=1.0和t_c=6.0a时,单位补充量最大群体产量为1492g。由此认为,现阶段牙鲆资源利用的最佳策略是通过增殖放流,增加资源补充;同时应适当控制捕捞压力,减少渔具对幼鱼资源的破坏并增设繁殖保护区,以追求最大持续产量。     

Relative abundance, age, growth, and fecundity of grubby Myoxocephalus aenaeus in Niantic River and Niantic Bay, Long Island Sound

Grubby (Myoxocephalus aenaeus, Cottidae) is a common benthic fish of inshore waters and estuaries of eastern Long Island Sound; however, little information exists on their life history or population demographics. This study utilised a long-term data series (1976–2002) to assess grubby life history and population demographics and explores trends in the Niantic River and Niantic Bay populations. In addition, we examined the age, size, and fecundity of adult grubby in 2001–02 to determine the population characteristics in the region. Mean grubby catch per unit effort (CPUE) in Niantic Bay ranged from 0.4 per trawl in 1976 to 2.9 per trawl in 1984 while river CPUE ranged from 0.4 per trawl in 1977 to 7.6 per trawl in 1989. Catch of grubby in bottom trawls varied seasonally with highest CPUE occurring in winter. Highest entrainment of grubby larvae occurred in 2001 while the lowest entrainment observed was in 1991. Four age classes, 0+ through III+, were derived from otolith analysis (N = 51) although length frequency analysis suggested the possibility of older fish in the population. The total number of eggs in ovaries ranged from 286 to 16 451 for grubby (N = 64) between 52 mm and 155 mm TL. Results of this study indicated a decline in abundance of adult grubby over the 26-year period, possibly related to concurrent declines in eelgrass (Zostera marina) abundance and/or increased water temperature.     

石盐的36Cl断代法

讨论了~936)Cl的成因、~(36)Cl断代法的原理及测试方法。自1987年以来,应用该方法测得柴达木盆地尕斯库勒湖和大浪滩湖石盐的沉积年龄,并与~(14)C,~(230)Th和古地磁测年法所测得的年龄数据进行对比,结果均在误差(1δ)范围内相吻合,表明石盐的~(36)Cl断代法是可行的,获得的年龄数据是可靠的。     

珠江口河流输沙、河口沉积与粒度信息之间的联系

河口三角洲地区泥沙供应充分，是现代沉积速率较高的区域。快速沉积的泥沙包含高分辨率的环境信息。采用放射性同位素测年方法研究了珠江口伶仃洋大铲湾海域6个柱样的现代沉积速率，以2mm的间隔分析了其中2个柱样上部的粒度，并对其平均粒径和珠江流域的年输沙量进行了快速傅里叶变换，以期获取河流泥沙供应、河口沉积速率和沉积物垂向粒度变化的对应关系。结果表明，大铲湾海域的沉积速率为1～3cm／a，受动力条件和泥沙供应条件的影响显著。2个柱样的平均粒径的最显著重现周期与珠江年输沙量的周期性有较好的对应关系，并可能反映了季节的、年的和多年的沉积速率信息。对于每年沉积厚度在厘米级的环境，以毫米级的高分辨率进行粒度分析，有可能揭示出沉积物供应的季节变化和年际变化。本研究亦可为其他河口的相关工作提供借鉴。     

Spatial variability in growth and reproduction of the Pacific oyster Crassostrea gigas (Thunberg, 1793) along the west European coast

The Pacific oyster Crassostrea gigas was introduced in Europe for commercial purposes in the mid 1960s. It was initially thought that low winter temperatures would restrain this species' reproduction and settlement; however, its present distribution in areas where no introduction has taken place suggests that natural invasion and expansion has occurred. Along the European coast, wild populations of Pacific oysters are already found from northern Germany to southern Portugal. Whether C. gigas will continue to further expand through northern waters will depend on its physiological performance. In this study, the performance of wild oyster populations has been studied in terms of growth and reproduction at three stations: La Rochelle (France; 46°N), Yerseke (Oosterschelde estuary, The Netherlands, 51°N), and Texel (Wadden Sea estuary, The Netherlands, 53°N). The French population had the lowest somatic-shell mass ratio and an increase in maximum shell length, somatic and gonadal mass was observed from France to the Netherlands. In addition, mean oocyte diameter decreased significantly from south to north. The combination of increasing gonadal mass and decreasing oocyte volume suggests an increasing reproductive output in terms of egg numbers from France to The Netherlands. Differences in temperature between locations will at least be partly responsible for the observed patterns; however, other environmental factors (such as food availability, predation pressure, sediment type and/or seston concentration) cannot be excluded. Since smaller eggs (oocytes) are thought to have a longer development time, the environmental conditions along the Dutch coast may result in increased larval dispersal and possibly in further population expansion.