高压超高压变泥质岩适用的地质温压计评述

高压超高压变泥质岩形成温压条件及p-T演化轨迹是高压超高压变质作用研究的重要内容。本文介绍了高压超高压变泥质岩适用的几种地质温压计,包括石榴子石-多硅白云母Fe~(2+)-Mg交换温度计、石榴子石-绿泥石Fe~(2+)-Mg交换温度计、硬绿泥石-绿泥石Fe~(2+)-Mg交换温度计、多硅白云母Si含量压力计、金红石Zr含量温度计、榍石Zr含量温压计、锆石Ti含量温度计、石英Ti含量温度计以及氧同位素温度计,并对上述温压计的适用条件及使用时的注意事项做了简要评述。     

广西桂林凉风洞秋冬季滴水和沉积物氧同位素对极端降水的记录研究

近年来,全球环境变化导致的极端气候事件的发生频率剧增,引起了国内外学者的广泛关注。由于器测记录时间较短,因此需要通过精确连续记录古气候变化的石笋来解译极端气候事件的规律。本文针对桂林凉风洞2015年9月至2016年1月的大气降水、洞穴滴水和现代沉积物的氧同位素组成进行了高分辨率的监测。监测结果揭示了由于秋冬水汽源的改变,导致桂林地区大气降水δD、δ~(18)O同位素值显示逐渐偏正的季节性变化,并且建立了该区域大气降水线为:δD=8.8δ~(18)O+16.38。由于大气降水作为凉风洞水源补给唯一来源,使得洞穴滴水的δ~(18)O继承大气降水的δ~(18)O所蕴含的环境信息,进而记录在洞穴现代沉积物中。但是受到洞穴顶部岩溶表层带的平滑或者均一化的作用,使得洞穴滴水的δ~(18)O同位素值要偏正于大气降水的δ~(18)O同位素值。在极端降水信号输入岩溶表层带后由于存在不同的水文地球化学过程,从而导致洞穴沉积物对其极端降水事件的响应时间存在不同,并且在δ~(18)O同位素值也存在明显差异。因此,系统监测洞穴滴水、沉积物δ~(18)O同位素对外界环境信息的响应过程,能为量化或精确解译石笋δ~(18)O同位素记录所指代的古气候环境信息提供基础。     

羌塘盆地热觉茶卡-藏夏河地区泉水水化学特征及其地质意义

泉水的水化学特征可以反映氧化-还原环境和水动力条件,近年来被广泛地用于石油、天然气以及天然气水合物的找矿工作中。本文对羌塘盆地热觉茶卡—藏夏河地区37处泉水和13件地表水进行了水化学特征、水溶性烃类气体特征和水中氢氧同位素特征分析,结果表明,羌塘盆地热觉茶卡—藏夏河地区的水型主要为Na₂SO₄型和MgCl₂型,其次为NaHCO₃型和CaCl₂型。矿化度普遍较高,说明该区具有较好的保存条件。铵根离子的平均含量为0.895 g/g,在藏夏河地区高达7.381 g/g,表明在藏夏河东部地区有机质相对较为丰富,这与区域上发育的富有机质页岩结果一致。氢氧同位素结果显示,该区水体的氢氧同位素落在了大气降水线附近,表明水体的来源主要受大气降水的补给。另外,采集的9个泉水样品中均检测出一定含量的水溶甲烷,在白云湖地区的甲烷含量相对较高,显示出较好的油气潜力。综合研究表明,藏夏河东和白云湖地区具有良好的油气烃源岩条件,保存条件较好,显示出良好的油气和天然气水合物资源前景。     

鲁西地区角闪石岩地球化学、矿物学特征及其地质意义

基性-超基性岩脉群通常形成于伸展构造背景,是示踪地幔源特征以及大陆和超大陆破裂的重要标志.鲁西地区角闪石岩为研究古元古代岩浆源和构造演化提供了一个窗口.本文对鲁西地区角闪石岩进行了岩相学、全岩地球化学及角闪石、黑云母电子探针原位分析.角闪石岩具板内构造环境,来自富集地幔.通过角闪石、黑云母成因分析,均具有幔源成因,角闪石结晶温度为702～781℃;结晶压力为29.8～228.8 MPa,结晶深度1～7.5 km,结晶时氧逸度变化范围在NNO+2.68到NNO+3.35之间.结合本次获得角闪石岩磷灰石U-Pb年龄为(1817±35)Ma,认为鲁西地区(1817±35)Ma处于板内拉伸环境,存在幔源岩浆上侵,已进入大陆裂解阶段.     

Characteristics of bottom dissolved oxygen in Long Island Sound,New York

The variability of bottom dissolved oxygen (DO) in Long Island Sound, New York, is examined using water quality monitoring data collected by the Connecticut Department of Environmental Protection from 1995 to 2004. Self-organizing map analysis indicates that hypoxia always occurs in the Narrows during summer and less frequently in the Western and the Central Basins. The primary factor controlling the bottom DO, changes spatially and temporally. For non-summer seasons, the levels of bottom DO are strongly associated with water temperature, which means DO availability is primarily driven by solubility. During summer, stratification intensifies under weak wind conditions and bottom DO starts to decrease and deviate from the saturation level except for stations in the Eastern Basin. For the westernmost and shallow (<15 m) stations, bottom DO is correlated with the density stratification (represented by difference between surface and bottom density). In contrast, at deep stations (>20 m), the relationship between oxygen depletion and stratification is not significant. For stations located west of the Central Basin, bottom DO continues to decrease during summer until it reaches its minimum when bottom temperature is around 19–20 °C. In most cases the recovery to saturation levels at the beginning of fall is fast, but not necessarily associated with increased wind mixing. Therefore, we propose that the DO recovery may be a manifestation of either the reduced microbial activity combined with the depletion of organic matter or horizontal exchange. Hypoxic volume is weakly correlated to the summer wind speed, spring total nitrogen, spring chlorophyll a, and maximum river discharge. When all variables are combined in a multiple regression, the coefficient of determination (r²) is 0.92. Surprisingly, the weakest variable is the total nitrogen, because when it is excluded the coefficient r² only drops to 0.84. Spring bloom seems to be an important source of organic carbon pool and biological uptake of oxygen plays a more crucial role in the seasonal evolution of bottom DO than previously thought. Our results indicate that the reassessment phase of the Long Island Sound Total Maximum Daily Load policy on nitrogen loading will most likely fail, because it ignores the contributions of the spring organic carbon pool and river discharge. Also, it is questionable whether the goal of 58.5% anthropogenic nitrogen load reduction is enough.     

Enhanced concentrations of dissolved gaseous mercury in the surface waters of the Arctic Ocean

During an almost three months long expedition in the Arctic Ocean, the Beringia 2005, dissolved gaseous mercury (DGM) was measured continuously in the surface water. The DGM concentration was measured using an equilibrium system, i.e. the DGM in the water phase equilibrated with a stream of gas and the gas was thereafter analysed with respect to its mercury content. The DGM concentrations were calculated using the following equation, DGM = Hg_eq / k_H' where Hg_eq is the equilibrated concentration of elemental mercury in the gas phase and k_H' is the dimensionless Henry's law constant at desired temperature and salinity. During the expedition several features were observed. For example, enhanced DGM concentration was measured underneath the ice which may indicate that the sea ice acted as a barrier for evasion of mercury from the Arctic Ocean to the atmosphere. Furthermore, elevated DGM concentrations were observed in water that might have originated from river discharge. The gas-exchange of mercury between the ocean and the atmosphere was calculated in the open water and both deposition and evasion were observed. The measurements showed significantly enhanced DGM concentrations, compared to more southern latitudes.     

Daily variability of dissolved inorganic radiocarbon at three sites in the surface ocean

We report radiocarbon measurements of dissolved inorganic carbon (DIC) in surface water samples collected daily during cruises to the central North Pacific, the Sargasso Sea and the Southern Ocean. The ranges of Δ¹⁴C measurements for each cruise (11–30‰) were larger than the total uncertainty (7.8‰, 2-sigma) of the measurements. The variability is attributed to changes in the upper water mass that took place at each site over a two to four week period. These results indicate that variability of surface Δ¹⁴C values is larger than the analytical precision, because of patchiness that exists in the DIC Δ¹⁴C signature of the surface ocean. This additional variability can affect estimates of geochemical parameters such as the air–sea CO₂ exchange rate using radiocarbon.     

Dissolved inorganic carbon (DIC) and its carbon isotopic composition in sediment pore waters from the Shenhu area,northern South China Sea

The Shenhu area is one of the most favorable places for the occurrence of gas hydrates in the northern continental slope of the South China Sea. Pore water samples were collected in two piston cores (SH-A and SH-B) from this area, and the concentrations of sulfate and dissolved inorganic carbon (DIC) and its carbon isotopic composition were measured. The data revealed large DIC variations and very negative δ ¹³C-DIC values. Two reaction zones, 0–3 mbsf and below 3 mbsf, are identified in the sediment system. At site SH-A, the upper zone (0–3 mbsf) shows relatively constant sulfate and DIC concentrations and δ ¹³C-DIC values, possibly due to bioturbation and fluid advection. The lower zone (below 3 mbsf) displays good linear gradients for sulfate and DIC concentrations, and δ ¹³C-DIC values. At site SH-B, both zones show linear gradients, but the decreasing gradients for δ ¹³C-DIC and SO₄ ²⁻ in the lower zone below 3 mbsf are greater than those from the upper zone, 0–3 mbsf. The calculated sulfate-methane interface (SMI) depths of the two cores are 10.0 m and 11.1 m, respectively. The depth profiles of both DIC and δ ¹³C-DIC showed similar characteristics as those in other gas hydrate locations in the world oceans, such as the Blake Ridge. Overall, our results indicate an anaerobic methane oxidation (AMO) process in the sediments with large methane flux from depth in the studied area, which might be linked to the formation of gas hydrates in this area.     

温度对管角螺Hemifusus tuba(Gelin)耗氧率和排氨率的影响

设置5个温度梯度(14、19、24、29、34℃),海水盐度为32,研究温度和规格对管角螺Hemifusustuba(Gelin)耗氧率和排氨率的影响。结果表明:14～29℃范围内,管角螺耗氧率随温度的升高,29℃时达到最大值;14～34℃范围内,排氨率随温度的升高而增加。在相同温度下,耗氧率和排氨率随单位软体部干重的增加而下降,管角螺软体部干重(W)与单位体重耗氧率(OR)、排氨率(NR)之间的关系分别符合幂函数方程OR=aW-b、NR=cW-d,W与OR、NR呈负相关关系。     

氨氮急性攻毒对水产经济动物棘胸蛙(Paa spinosa)蝌蚪死亡率、排氨率、耗氧率及窒息点的影响

以体长(1.932±0.204)cm、体质量(1.386±0.055)g的棘胸蛙蝌蚪为实验动物,在水温(24±0.2)℃、DO(7.30±0.01)mg/L、pH 7.30±0.01条件下,采用静水停食法开展了氨氮对蝌蚪的急性攻毒实验,并以此为基础,测定了不同氨氮质量浓度胁迫下棘胸蛙蝌蚪的排氨率、耗氧率、氧氮比及窒息点。结果表明:(1)蝌蚪对氨氮急性攻毒具明显的运动避毒行为,濒死个体的背部皮肤和肝脏均具明显的色变症状;(2)氨氮对蝌蚪的急性致死率具明显的剂量—时间效应,24h、48h、72h、96h LC50依次为177.5、151.7、148.6和146.8mg/L,毒性时段蓄积程度系数呈持续下降趋势,24—48h、48—72h、72—96h的时段MAC值分别为84.04%、10.1%和5.86%;(3)蝌蚪夜均、昼均、日均及时段排氨率随氨氮质量浓度增加均呈阶梯式下降趋势,其中时段排氨率与对照组均无显著差异的为9.80mg/L实验组,夜均、昼均、日均及时段排氨率与对照组均无显著差异的仅为2.45mg/L实验组(P0.05);(4)氨氮对蝌蚪呼吸耗氧具低毒兴奋效应,其夜均、昼均和日均耗氧率随氨氮质量浓度增加均呈先升后降趋势,峰值氨氮质量浓度范围均为4.90—7.35mg/L(P0.05),与对照组均无显著差异的仅为14.70mg/L实验组(P0.05),窒息点含氧量随氨氮质量浓度增加呈先降后升趋势,谷底出现于4.90mg/L实验组(P0.05),与对照组无显著差异的仅为9.80mg/L实验组(P0.05);(5)实验期间,蝌蚪氧氮比(O:N)波动于18.87—25.34之间,昼均和日均氧氮比(O:N)随氨氮质量浓度增加均依次呈"上升—稳定—下降—再稳定"之趋势,两者的峰值氨氮质量浓度范围分别为4.90—14.70mg/L和4.90—9.80mg/L,夜均氧氮比(O:N)呈先升后降趋势,峰值出现于7.35mg/L实验组(P0.05)。