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31.
Taking continuous spatiotemporal in situ measurements with multi‐probes in fast‐flowing waters/rivers can be problematic because the sensors may be damaged by high shear forces and flotsam. To protect the multi‐probe and to enable easy access for the maintenance and calibration of the sensors, a special multi‐probe holder fixed in a hydrographic slot was developed. The validation of the probe system revealed a “memory effect” at short time scales (< 10 s) within sharp gradients caused by the overflow container of the multi‐probe rack keeping the sensors submerged in the sample water. Continuously recorded data (conductivity, temperature, pH, oxygen concentration and saturation, as well as in vivo fluorescence of chlorophyll‐a) from a research cruise on board the RV ALBIS along the river Elbe (river km 309) and entering the river Saale are presented. This river stretch upstream of the city of Magdeburg to the mouth of the Saale tributary was found to have a complex physicochemical character, which is attributable to the long mixing process of water from the river Saale and the river Elbe.  相似文献   
32.
13C/12C and 18O/16O ratios of aragonite shells of modern land snails from the southern Great Plains of North America were measured for samples from twelve localities in a narrow east-west corridor that extended from the Flint Hills in North Central Oklahoma to the foothills of the Sangre de Cristo Mountains in Northern New Mexico, USA. Across the study area, shell δ18O values (PDB scale) ranged from −4.1‰ to 1.2‰, while δ13C values ranged from −13.2‰ to 0.0‰. δ18O values of the shell aragonite were predicted with a published, steady state, evaporative flux balance model. The predicted values differed (with one exception) by less than 1‰ from locality averages of measured δ18O values. This similarity suggests that relative humidity at the time of snail activity is an important control on the δ18O values of the aragonite and emphasizes the seasonal nature of the climatic information preserved in the shells. Correlated δ13C values of coexisting Vallonia and Gastrocopta suggest similar feeding habits and imply that these genera can provide information on variations in southern Great Plains plant ecology. Although there is considerable scatter, multispecies, transect average δ13C values of the modern aragonite shells are related to variations in the type of photosynthesis (i.e., C3, C4) in the local plant communities. The results of this study emphasize the desirability of obtaining isotope ratios representing averages of many shells in a locale to reduce possible biases associated with local variations among individuals, species, etc., and thus better represent the “neighborhood” scale temporal and/or spatial environmental variations of interest in studies of modern and ancient systems.  相似文献   
33.
改则盆地位于青藏高原腹地,盆地内沉积物记录了高原古环境变化的重要信息。本文对改则盆地康托组碳酸盐岩碳氧同位素进行研究,结果显示改则盆地中-晚始新世的演化分为两个阶段:1中始新世湿润气候下开放湖盆阶段:虽然碳酸盐岩δ~(18)O值在43层处向正值偏移,但整体~(18)O和~(13)C强烈亏损,并且该时期碳酸盐岩δ~(18)O值和δ~(13)C变化相关系数为R~2=0.082。表明该阶段的研究区虽然经历过短期蒸发作用增强或补给水减少,但整体是气候湿润条件下补给水丰富的开放型湖盆。2晚始新世干旱气候下封闭湖盆阶段:经过中新世晚期(63层)气候和湖泊水文状态的过渡,晚始新世~(18)O和~(13)C同位素富集,δ~(18)O值和δ~(13)C值变化相关系数为R~2=0.7762。表明该阶段气候干旱,蒸发作用强烈,湖盆萎缩成为封闭湖盆。综合前人研究,认为青藏高原腹地及北缘、东北缘在晚始新世存在明显的区域性干旱化事件。对比分析青藏高原隆升、全球气候记录、全球海水Sr和大气CO_2记录,认为青藏高原腹地和北部的干旱化事件主要受青藏高原隆升的影响。  相似文献   
34.
Granitic magmatism in the Cachoeirinha‒Salgueiro and Alto Pajeú terranes in the Transversal Zone Domain of the Borborema Province, northeastern Brazil, occurred in three main time intervals: 650–620 Ma, 590–560 Ma and 545–520 Ma. The oldest one is characterized by intrusions of magmatic-epidote (mEp) bearing calc-alkalic (some with trondhjemitic affinities) and high-K calc-alkalic plutons, synkinematic to the main regional foliation, under contractional tectonic regime, and exhibits TDM < 2.0 Ga and ƐNd (0.6 Ga) from −1 to −4, and δ18O (zircon) values from 7.1 to 10‰VSMOW. O- and Nd-isotope data for the 650‒620 Ma group of plutons is compatible with partial fusion of subducted oceanic basaltic crust (mEp-bearing calc-alkalic tonalites/granodiorites, equivalent to adakites). Voluminous intrusions in the 590–560 Ma interval are represented by abundant mEp-free high-K calc-alkalic, peralkalic, ultrapotassic, mEp-bearing high-K calc-alkalic, and less abundant shoshonitic magmas. Nd-model ages for this group of plutons vary from 1.5 to 2.5 Ga and ƐNd (0.6 Ga) ranges from −8 to −20; δ18O (zircon) varies from 6.4 to 7.9‰VSMOW. Values of δ18O (zircon) for the 590‒560 Ma old group of plutons coupled with Nd isotope data are compatible with remelting of crustal (negative ƐNd, 1.6 to 2.0 Ga old) source rocks. O- and Nd-isotope data for this group of plutons are compatible with underplating of basaltic magma in the base of the lower crust for the high-K calc-alkalic granitoids, coeval to transcurrent movements along sigmoidal shear zones. Intrusion of one shoshonitic (Serrote do Arapuá), one calc-alkalic (Riacho do Icó) plutons besides the peralkalic Manaíra-Princeza Isabel dike set have witnessed this transition from contractional to transcurrent movements along shear zones, around 610‒600 Ma.  相似文献   
35.
The Fengjia barite–fluorite deposit in southeast Sichuan is a stratabound ore deposit which occurs mainly in Lower Ordovician carbonate rocks. Here we present results from fluid inclusion and oxygen and hydrogen isotope studies to determine the nature and origin of the hydrothermal fluids that generated the deposit. The temperature of the ore‐forming fluid shows a range of 86 to 302 °C. Our detailed microthermometric data show that the temperature during mineralization of the fluorite and barite in the early ore‐forming stage was higher than that during the formation of the calcite in the late ore‐forming stage. The salinity varied substantially from 0.18% to 21.19% NaCl eqv., whereas the density was around 1.00 g/cm3. The fluid composition was mainly H2O (>91.33%), followed by CO2, CH4 and traces of C2H6, CO, Ar, and H2S. The dominant cation was Na+ and the dominant anion Cl, followed by Ca2+, SO42‐, K+, and Mg2+, indicating a mid–low‐temperature, mid‐low‐salinity, low‐density NaCl–H2O system. Our results demonstrate that the temperature decreased during the ore‐forming process and the fluid system changed from a closed reducing environment to an open oxidizing environment. The hydrogen and oxygen isotope data demonstrate that the hydrothermal fluids in the study area had multiple sources, primarily formation water, as well as meteoric water and metamorphic water. Combined with the geological setting and mineralization features we infer that the stratabound barite–fluorite deposits originated from mid–low‐temperature hydrothermal fluids and formed vein filling in the fault zone.  相似文献   
36.
Aubrites are achondritic meteorites (enstatite pyroxenites) that were formed in highly reduced magmatic environments on a differentiated parent body sharing a common oxygen isotope reservoir with enstatite chondrites (EC), Earth and Moon, and could be considered as a geochemical model of the early proto-Earth. Some pyroxenes of the Pesyanoe aubrite have high abundance of gaseous inclusions, captured during the crystallization of the rocks. Investigation of the inclusions by IR spectroscopy reveals presence of OH groups and C–H bonds. The former are assigned to protonated point defects in enstatite lattice and the latter to compounds occupying void walls. Molecular water and CO2 were not observed. Volatile components released from the samples of the Pesyanoe enstatite by stepwise crushing and heating are composed of CO2, H2O and a non-condensable phase. Hydrogen isotopic composition of volatiles extracted in form of molecular water in Px-separates varies in the range δD = −61 – −84‰ with mean value of δD = −73 ± 16‰ VSMOW and is within the ranges of ECs and Earth’s mantle. The total abundance of H2 in the pyroxene of Pesyanoe were estimated as at least 0.047 ppm that is too low in comparison with that of enstatite chondrites (≥30 ppm H2) and could indicate nearly complete degassing of the Pesyanoe primitive precursor material during the Pesyanoe parent body accretion or a mantle degassing in igneous differentiation process. In a last case a primitive precursor could have D/H ratio different from that of enstatite chondrites.  相似文献   
37.
丁青蛇绿岩位于班公湖-怒江缝合带东段,是该缝合带出露面积最大的蛇绿岩。为查明岩体成因,在丁青东岩体中实施了一口165.19m的钻孔。除最顶部有约0.5m厚的第四系残坡积物外,其余均为地幔橄榄岩。结合显微镜鉴定将岩心划分出17个岩性单元层,岩性主要以方辉橄榄岩为主,夹少量纯橄岩和含铬铁矿纯橄岩。地幔橄榄岩中橄榄石的Fo变化于88.79~93.73,铬尖晶石的Cr#变化于44.33~81.66,揭示丁青地幔橄榄岩可能经历过约20%~40%的中高度部分熔融作用;全岩地球化学分析表明其具有富镁(MgO=45.98%~49.45%)、贫铝(Al2O3=0.19%~1.37%)和贫钙(CaO=0.28%~0.70%)的特点,属于熔融程度较高的地幔残余物质。岩石具有明显不同于阿尔卑斯蛇绿岩的轻稀土元素富集特征,指示区内地幔橄榄岩先经历了较强程度的部分熔融,后经历了俯冲消减过程中的流体交代。利用地幔橄榄岩中的铬尖晶石成分计算母熔体Al2O3含量对应的FeO/MgO值,与不同构造环境原始岩浆成分相比较,发现丁青地幔橄榄岩母熔体大多处于玻安岩中。纯橄岩氧逸度估算FMQ=-3.05~-0.71,方辉橄榄岩氧逸度FMQ=-3.89~+1.47,显示丁青地幔橄榄岩有俯冲作用的参与。通过丁青钻孔岩心的研究,提出丁青东岩体可能形成于俯冲带之上的弧前环境这一观点。  相似文献   
38.
王家录  任娟  王勇  李维杰  娄昭  陈佳 《热带地理》2020,40(2):335-345
为探究岩溶水库水文地球化学行为过程,对贵州普定夜郎湖表层水体进行了为期3 d的高分辨率昼夜监测。结果表明:1)多变的天气和水文条件叠加导致水体离子指标昼夜变化不显著,规律性较差。而水温、DO、pH值、SpC、SIc、pCO2等常规理化指标受水温变化和生物作用表现出明显的昼夜波动。2)利用亨利常数和主成分分析,得到温度变化、生物作用、人类活动、水库的蓄水与放水对夜郎湖水库水文地球化学特征变化的贡献率分别为21.66%、17.28%、14.08%和10.22%,说明作用于水库水文地球化学行为的因子具有多元性。3)δ 18O表现出与DO一致的波动趋势,即白天上升,晚上下降,反映在短时间尺度上,氢氧稳定同位素变化受控于生物过程(主要是呼吸作用过程);而对比水库水体和大气降水的d-excess(d值)发现,水库水体的d值(8.21‰)显著偏低于当地大气降水的d值(9.64‰),说明在长时间尺度上,主要受蒸发效应引起的不平衡分馏影响。  相似文献   
39.
采用室内实验生态学方法对华贵栉孔扇贝的耗氧率和排氨率进行了研究。旨在为华贵栉孔扇贝养殖容量的调查及生态生理的研究提供参考,并可为海洋生态系统动力学和贝类能量学研究提供科学依据。实验结果表明,在实验温度(13—33℃)范围内,华贵栉孔扇贝的耗氧率(OR)和排氨率(NR)与体重(W)都呈负相关,可以用Y=aW-b表示。华贵栉孔扇贝的耗氧率和温度的关系可以表示为OR=-c+b1T-b2T2。在13—28℃温度范围内,华贵栉孔扇贝的耗氧率随温度的升高而增加,28℃时,耗氧率达到最大值,温度升高到33℃时,耗氧率反而下降。而排氨率与温度的关系可以表示为1NR=c1edT,在实验温度范围内,排氨率随温度的升高则呈持续升高趋势。华贵栉孔扇贝呼吸和排泄Q10值范围分别为0.466—2.471和1.129—2.437。在23—28℃温度范围内,不同规格华贵栉孔扇贝的耗氧率和排氨率的比值(原子数O:N)较高。方差分析表明,体重、温度及二者的交互作用对华贵栉孔扇贝的耗氧率和排氨率均有极显著的影响(P0.01)。华贵栉孔扇贝的日常代谢明显高于标准代谢,耗氧率和排氨率平均值分别提高29.9%和69.4%。  相似文献   
40.
Dissolved oxygen in seawater has been determined by using the Winkler's reaction scheme for decades. An interference in this reaction scheme that has been heretofore overlooked is the presence of naturally occurring iodate in seawater. Each mole of iodate can result in an apparent presence of 1.5 mol of dissolved oxygen. At the concentrations of iodate in the surface and deep open ocean, it can lead to an overestimation of 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg− 1 of oxygen in these waters respectively. In coastal and inshore waters, the effect is less predictable as the concentration of iodate is more variable. The solubility of oxygen in seawater was likely overestimated in data sources that were based on the Winkler's reaction scheme for the determination of oxygen. The solubility equation of García and Gordon [Garcia H.E., Gordon, L.I., 1992. Oxygen solubility in seawater: Better fitting equations. Limnol. Oceanogr. 37, 1307–1312] derived from the results of Benson and Krause [Benson, F.B., Krause, D. Jr., 1984. The concentration and isotopic fractionation of oxygen dissolved in freshwater and seawater in equilibrium with the atmosphere. Limnol. Oceanogr. 29, 620–632] is free from this source of error and is recommended for general use. By neglecting the presence of iodate, the average global super-saturation of oxygen in the surface oceans and the corresponding efflux of oxygen to the atmosphere both have been overestimated by about 8%. Regionally, in areas where the degree of super-saturation or under-saturation of oxygen in the surface water is small, such as in the tropical oceans, the net air–sea exchange flux can be grossly under- or overestimated. Even the estimated direction of the exchange can be reversed. Furthermore, the presence of iodate can lead to an overestimation of the saturation anomaly of oxygen in the upper ocean attributed to biological production by 0.23 ± 0.07%. AOU may have been underestimated by 0.52 ± 0.15 and 0.63 ± 0.05 μmol kg− 1 in the surface mixed layer and deep water, while preformed phosphate and preformed nitrate may have been overestimated by 0.004 ± 0.001 and 0.06 ± 0.02 μmol kg− 1 in the surface mixed layer, and 0.005 ± 0.0004 and 0.073 ± 0.006 μmol kg− 1 in the deep water. These are small but not negligible corrections, especially in areas where the values of these parameters are small. At the increasing level of sophistication in the interpretation of oxygen data, this source of error should now be taken into account. Nevertheless, in order to avoid confusion, an internationally accepted standard needs to be adopted before these corrections can be applied.  相似文献   
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