989 resultados para Helium and argon isotopes


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The Tianshan Mountains is located about 1000-2000 km north of the India-Asia suture and is the most outstanding topography in central Asia, with transmeridional length of nearly 2500 km, north-southern wideness of ~ 300-500 km, peaks exceeding 7000 m above sea level (asl.), and average altitude of over 4000 m asl. Much of the modern relief of the Tianshan Range is a result of contraction driven by the collision of the India subcontinent with the southern margin of Asia, which began in early Tertiary and continues today. Understanding where, when and how the deformation of the Tianshan Mountains occurred is essential to decipher the mechanism of intracontinental tectonics, the process of foreland basin evolution and mountain building, and the history of climate change in central Asia. In order to better constrain the Cenozoic building history of the Tianshan Mountains and the climate change in the southern margin of the Junggar Basin, we carried out multiple studies of magnetostratigraphy, sedimentology, and stable isotopes of paleosol carbonate at the Jingou River section, which is located at the Huoerguosi anticline, the westernest one of the second folds and thrust faults zone in the northern piedmont of the Tianshan Mountains. The Jingou River section with a thickness of about 4160 m is continuous in deposits according to the observed gradual change in sedimentary environments and can be divided into five formations: Anjihaihe, Shawan, Taxihe, Dushanzi and Xiyu in upward sequence. Characteristic remamences were isolated by progressive thermal demagnetization, generally between 300 and 680℃. A total of 1133 out of 1607 samples yielded well-defined ChRMs and were used to establish the magnetostratigraphic column of a 3270-m-thick section from the exposed base of the Anjihaihe Formation to the middle of the Xiyu Formation. Two vertebrate fossil sites and a good correlation with the CK95 geomagnetic polarity time scale suggest that the section was deposited from ~30.5 to ~4.6 Ma and the age of the top of the Xiyu formation is ~2.6 Ma based on an extrapolation of the sedimentation rates. A plot of magnetostratigraphic age vs. height at the Jingou River section shows that significant increases in sedimentation rates as well as notable changes in depositional environments occurred at ~26-22.5 Ma, ~13-11 Ma and ~7 Ma, which represent the initial uplift of the Tianshan Mountains and two subsequent rapid uplift events. In addition, changes in sedimentation rates display characteristic alternations between increases and decreases, which probably indicate that the uplift of the Tianshan Mountains was episodic. We discussed the history of C4 biomass and climatic conditions in the southern margin of the Junggur Basin using the stable carbon and oxygen isotope composition of paleosol carbonates from the Jingou River section during ~17.5-6.5 Ma. The δ13C values indicate that the proportion of C4 biomass was uniform and moderate (15-20 %) during the interval of ~17.5-6.5 Ma. We proposed three hypotheses for this pattern of C4 biomass: (1) counteraction of two opposed factors (global cooling since ~15 Ma and thereafter increased dry and seasonality in central Asia) controlling the growth of C4 grasses, (2) variability in abundance of C3 grasses relative to C3 trees and shrubs if vegetation had ever changed in ecosystems, and (3) the higher latitude of the studied region. The δ18O values show a stepwise negative trend since ~13 Ma which may be attributed to three factors: (1) the temperature decreasing gradually after the middle Miocene (~15 Ma), (2) the increasing contribution of the moistures carried by the polar air masses from the Arctic Ocean to precipitation, and (3) the gradual retreat westward and disappearance of the Paratethys Ocean. Among them, which one played a more important role will need further study of the paleoclimate in central Asia.

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Through field outcrop dolomite observation, laboratory petrography (macroscopy, microscopy, cathodeluminescence and scan electronic microscopy), geochemistry (carbon-oxygen-strontium isotopes and trace elements) and fluid inclusion microthermometry study in Keping-Bachu area of Tarim Basin, it can be inferred that there are existing eight dolomite texture types within four evolution phases in Keping-Bachu area of Tarim Basin. The paragenesis of different dolomite texture types and associated minerals in Keping-Bachu area has been established. The carbon and oxygen isotopes of saddle dolomites and matrix dolomites overlap greatly. The Strontium isotopes results of Keping-Bachu outcrop area show that the strontium isotopes differentiation of the matrix and saddle dolomites is not obvious, the reason of which is that there is thousands of Cambrian-Ordovician dolomite strata below the stratum bearing the saddle dolomite. In the process of the heat flow upward migration, the isotopes of the heat interacts with the host rock, which leads to the similarity betwwen the strontium of the saddle dolomite and matrix dolomite. The strontium isotope of the saddle dolomite is not very radiogenic. the six types samples within four phases in the study area show Eu negatively. Comparing to the other types of samples, the δEu of saddle dolomite is relatively high falling into the range of 0.510-0.874, which shows that the saddle dolomite forms in the hydrothermal setting and is affected by the hydrothermal activity to some extend.The Lan/Ybn of saddle dolomite is high up to 15.726, which means that the HREE is very rich. It belongs to the typical hydrothermal genesis model. The δCe of saddle dolomite is positive anomaly, which is the result of high effect from the land source debris. The homogeneous temperature of the saddle dolomite falls into two ranges 110-120℃ and 125-160℃, after pressure correction, they are 141-152℃,157.5-196℃, the salinity of the saddle dolomite can reach to 20-25%. With the comparing with the burial history, the Th of the saddle dolomite is high than the ambient strata temperature, these data show that the saddle dolomite is of hydrothermal origin. The evolution trend of different dolomite and associated minerals is from matrix dolomite, dolomite cementation, saddle dolomite, quartz to calcite. Alonging with this evolution trend, the temperature of the diagenetic flow initiated from 80-100℃, after rising to 135-160℃, then gradually declined. Finally, a structurally-controlled dolomitization model is established in Keping-Bachu area of Tarim Basin.

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A number of proxy records of paleoenvironment using stable isotopes could show the history of past environmental changes. These archives include peat and lake sediments, loess-paleosot sequence, fossil mammals and stalagmite, and so on. The stable isotopic composition of carbonate and organic matter and frequency magnetic susceptibility from Tianshuigou and Yuanlei loess-palesol sequence can be used to give estimates of the paleoenvironmental history of Dali, and even of the whole Chinese Loess Plateau during the last 250ka. Features of the High Temperature and Large Precipitation Event in the Tibet Plateau and its adjacent area during 40~30kaBP had been studied by Professor Shi Y. In this dissertation, its impact on Chinese Loess Plateau has been discussed again. Carbon and oxygen isotopic ratios, magnetic susceptibility and frequency magnetic susceptibility in Tianshuigou and Yuanlei profiles show that the Event in this area is not so stronger as the Tibet Plateau. The carbon isotopic composition of organic matter in Tianshuigou, Yuanlei, dingcun and Jingcun loess-palesol sequences are indicative of major changes in the paleovagetation between terrace and plain of the Chinese Loess Plateau. Water is one of the most important factors adjusting the relative biomass of C4 plant in terrestrial ecosystems. Stable carbon isotope ratio of vertebrate tooth enamel is used increasingly to reconstruct environmental and ecological information modern and ancient ecosystems. The SI3C value of tooth enamel bioapatites can distinguish between browsers and grazers. Data from typical grassland of Inter Mongolia, the Alpine meadow of Qinghai-Tibet Plateau and the Yaluzangbu Great Canyon indicate that diets of mammals could record the relative biomass of C4 plant only in the C4 dominated ecosystem. In a C3 dominated ecosystem, diet of mammals would include more C3 plants than vegetation. According to Professor Cerling, proxy records from North and South America, Africa and Pakistan show that at the end of the Miocene (between 8Ma to 6 Ma) there was a global expansion of CA biomass, probably when atmospheric CO2 levels declined. Thus, "C4 world" and "CO2 starvation" are put forward. In this dissertation, carbon isotopes of fossil tooth such as Equus sanmeniensis and Hipparion chiai from Linxia, China reveal that there is a C3 dominated ecosystem in the late Miocene. Diets of ancient mammals in Linxia are not evidence of global expansion of C4 biomass.

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Data on seawater carbon isotope in the Mesoproterozoic and Neoproterozoic is abundant. However, the sulfur isotopic age curve of seawater sulfates determined through the analysis of sulfur isotopic composition of marine evaporite is uncertain in the Mesoproterozoic and Neoproterozoic since evaporites are generally rare in Precambrian. The Mesoproterozoic and Neoproterozoic Carbonate Formations preserve not only the carbon isotopic records, but also the sulfur isotopic records of coeval seawater in the Huabei Platform and the Yangtze Platform, China. Sulfur isotopic composition can be determined by the extraction of trace sulfate from carbonate samples. Successive measurements of sulfur and carbon isotopic compositions of carbonate samples from the Mesoproterozoic and Neoproterozoic strata in the Huabei Platform and the Yangtze Platform was accomplished through the extracting of trace sulfate from carbonates. Sulfur and carbon isotopic compositions of coeval seawater were obtained from analytical results of sulfur and carbon isotopes of the same sample without diagenetic alteration. The high-resolution age curve of sulfur isotope given in this paper may reflect the trend of variations in sulfur isotope composition of seawater sulfates during the Mesoproterozoic and Neoproterozoic. It can be correlated with the characteristics of variation in age curve of carbon isotope of coeval seawater carbonates. The δ34S values of seawater varied from +10.3-37.0‰ during the Mesoproterozoic, which took on oscillated variation on the whole. The δ34S values took on high values in the Mesoproterozoic Chuanlinggou stage, Tuanshanzi stage Tieling stage and in Neoproterozoic Jing'eryu stage. The average of those was about +30‰. The sulfates have low δ34S values in the Mesoproterozoic Yangzhuang stage and Hongshuizhuang stage, The average of those was all lower than +20‰. There occured large-amplitude changs in δ34S values of seawater during the Mesoproterozoic. Large-amplitude oscillate of 534S values occured in the intervals of 1600~1400Ma and 1300~1200Ma. The δ13C values of seawater are mostly negative in Changcheng stage of late Paleoproterozoic, -0 ± 1‰ range in Jixian stage of Mesoproterozoic , and the positive 2±2‰ commonly in early Neoproterozoic Jing'eryu stage. From 1000 Ma to 900 Ma, about 108 years interval of oceanic 513C record is shortage. At the end of Paleoproterozoic (1700 - 1600 Ma), the oceanic 813C values change from -3‰ to 0‰, but strongly oscillate near 1600 Ma. Two larger variations of seawater 513C values occur in the Mesoproterozoic: one is a cycle of about 4%o happens at ca. 1400 Ma; another is rise from >2‰ to>5‰ at ca. 1250 Ma and then become stable at the near 1000 Ma. There appears a large positive excursion over +20‰ in 534S value of ancient seawater sulfates in the early Doushantuo stage. Simultaneously, 8 C values of ancient seawater occur a positive excursion reaching 10‰. These allow δ4S values and 513C values to reach high values of+51.7‰ and +6.9‰, respectively. The range of variation in 834S values of seawater is relatively narrow and 513C values are quite high in the middle Doushantuo stage. Then, δ34S values of seawater become oscillating, the same happens in δ13C values. Negative excursions in 834S values and 813C values occur simultaneously at the end of the Doushantuo stage, and the minimum of δ34S values and δ13C values dropped to -11.3‰ and -5.7‰, respectively. The ancient seawater in the Dengying stage has high δS values and δ13C values. Most of the δ34S values of the trace sulfate samples varied between +23.6‰ and +37.9‰ except two boundaries of the Dengying Formation, and the S13C values of the carbonate samples of the Dengying Formation varied between +0.5‰ and +5.0‰. There appeared large negative excursion in 834S values and δ13C values of ancient seawater at the bounder of Precambrian-Cambrian. The isotopic characteristics of sulfur and carbon implicated that the organic productivity and isotopic fractionation caused by biology were low and the palaeoceanic environment was quite unstable during the Mesoproterozoic. The increase and subsequent oscillation of seawater δ13C value occurred from 1700 to 1600 Ma and near 1300 Ma may be responsible to the two global tectonic events happened at coeval time. The characteristics of variation in sulfur and carbon isotopes of ancient seawater imply strong changes in oceanic environment, which became beneficial to inhabitation and propagation of organism. The organic production and the burial rate of organic carbon once reached a quite high level during the Doushantuo stage. However, the state of environment became unstable that means the global climate and the environment possibly were fluctuating and reiterating after the global glaciation. The negative excursions of S34S values and δ13C values occurring at the end of the Doushantuo stage represent a global event, which might be relative to the oxidation of deep seawater. The isotopic characteristics of sulfur and carbon implicated that there were a high organic productivity and a high burial rate of organic carbon in the Dengying stage. It is obvious that the palaeoceanic environment in Dengying stage was stable corresponding and beneficial for biology to inhabit and propagate except for the two boundaries. The tendency of sulfur and carbon isotopic variations maybe resulted from the gradual oxygenation of ocean environment during the Dengying stage. It has been reported that the secular variations of the sulfur isotopic compositions in seawater was negative correlated with that of carbon isotopic compositions. However, our results show that it is not the case. They were negatively correlated in some intervals and positively in some other intervals of the Mesoproterozoic and Neoproterozoic. The difference in correlation may be associated with the changes in conditions of redox in oceanic environment, e.g. sharp change of the oxidation-reduction interface. The strong changes in global environment may induce the abnormality to occur in the biogeo chemical S and C cycles in the ocean and accordingly sharp Variations in isotopic composition of seawater sulfur and carbon during the Mesoproterozoic and Neoproterozoic. Simultaneously, the global tectonism caused large changes of 87Sr/86Sr ratios. The leading factor that causes the variation in isotopic composition is different in the different intervals of the Mesoproterozoic and Neoproterozoic. Thus, there may exist different models of the biogeochemical S and C cycles in the ocean during the Mesoproterozoic and Neoproterozoic.

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The Fanshan complex consists of layered potassic ultramafic-syenite intrusions. The Fanshan apatite (-magnetite) deposit occurs in the Fanshan complex, and is an important style of phosphorus deposit in China. The Fanshan complex consists of three (First- to Third-) Phases of intrusion, and then the dikes. The First-Phase Intrusive contains ten typical layered rocks: clinopyroxenite, biotite clinopyroxenite, coarse-grained biotite clinopyroxenite, pegmatitic orthoclase-biotite clinopyroxenite, variegated orthoclase clinopyroxenite, interstitial orthoclase clinopyroxenite, biotite rock, biotite-apatite rock, biotite rock and magnetite-apatite rock. This layered intrusive consists of nine rhythmic units. Each rhythmic unit essentially comprises a pair of layers: clinopyroxenite at the bottom and biotite clinopyroxenite at the top. The apatite (-magnetite) deposit is situated near the top of rhythmic Unit no. 6 of the First-Phase Intrusive. The Second-Phase Intrusive contains three typical rocks: coarse-grained orthoclase clinopyroxenite, . coarse-grained salite syenite and schorlomite-salite syenite. The Third-Phase Intrusive includes pseudo-trachytic salite syenite, porphyritic augite syenite, fine-grained orthoclase clinopyroxenite and fine-grained salite syenite. The origin of the Fanshan complex is always paid attention to it in China. Because most layered igneous intrusion in the world not only have important deposit in it, but also carry many useful information for studying the formation of the intrusion and the evolvement of magma. Two sketch maps were drawn through orebodies along no. 25 cross-cut on 425 mL and no. 1 cross-cut on 491 mL in the Fanshan mine. Through this mapping, a small-scaled rhythmic layering (called sub-rhythmic layering in the present study) was newly found at the top of the rhythmic Unit no. 6. The concept of sub-rhythmic layering is defined in this article. The sub-rhythmic layering is recognized throughout this apatite-rich part, except for magnetite-apatite rock. Presence of the layered magnetite-apatite rock is one of the characteristics of the Fanshan apatite (-magnetite) deposit. Thus, from this layer downwards six units of sub-rhythmic layering are recognized in the present study. Each unit consists of biotite clinopyroxenite (or biotite rock and biotite-apatite rock) layer at the bottom and apatite rock layer at the top. To study this feature in detail is an important work for understanding the origin of the Fanshan complex and apatite (-magnetite) deposit. The origin of the Fanshan complex and the relation of the formation of the apatite(-magnetite)deposit will be interpreted by the study of sub-rhythmic layering on the basis of previous research works. The magma formed the Fanshan complex was rich in K2O, early crystallized pyroxene, and after this phase more biotite crystallized, but no amphibole appeared. This indicated that the activity of H2O in the magma was low. Major element compositions of biotite and clinopyroxene (on thin sections) in the sub-rhythmic layering were analyzed using electron microprobe analyzer. The analytical results indicate Mg/(Mg+Fe*+Mn) atomic ratios (Fe*, total iron) of these two minerals rhythmically changed in sub-rhythmic layering. The trends of Mg/(Mg+Fe*+Mn) atomic ratio (Fe*, total iron) of biotite and clinopyroxene indicate that the magma evolved markedly from relatively magnesian bottom layer to less magnesian top layer in each sub-rhythmic unit. A general trend through the sub-rhythmic layering sequence is both minerals becoming relatively magnesian upwards. The formation temperatures for sub-rhythmic layering yield values between 600 and 800 ℃, were calculated using the ratio of Mg/(Mg+Fe+Mn) in the salite and biotite assemblage. The equilibrium pressures in the rhythmic layers calculated using the contents of Al in the salite were plotted in the section map, shown a concave curve. This indicates that the magma formed the First-Phase Intrusive crystallized by two vis-a-vis ways, from its bottom and top to its centre, and the magnetite-apatite rock was crytallized in the latest stage. The values of equilibrium pressures in the sub-rhythmic layering were 3.6-6.8(xlO8) Pa with calculated using the contents of Al in the salite. The characteristics of geochemistry in various intrusive rocks and the rocks or apatite of sub-rhythmic layers indicated that the Fanshan complex formed by the comagmatic crystallization. The contents of immiscible elements and REEs of apatite rock at the top of one sub-rhythmic unit are more than biotite clinopyroxenite at the bottom. The contents of immiscible elements and REEs of apatite of biotite clinopyroxenite at the bottom of one sub-rhythmic unit are higher than apatite rock at the top. The curves of rocks (or apatite) in the upper sub-rhythmic units are between two curves of the below sub-rhythmic unit in the primitive mantle-normalized trace element abundance spider diagram and the primitive mantle-normalized REE pattern. The trend for the contents of immiscible elements and REEs inclines to the same contents from the bottom to the top in sub-rhythmic layering. These characteristics of geochemistry of rocks or apatites from sub-rhythmic layering indicate that the latter sub-rhythmic unit was produced by the residual magma after crystallization of the previous sub-rhythmic unit. The characteristics of petrology, petrochemistry, geochemistry in the Fanshan complex and sub-rhythmic layers and the trends of Mg/(Mg+Fe+Mn) atomic ratio of biotite and clinopyroxene in sub-rhytmic layering rejected the hypotheses, such as magma immiscibility, ravitational settling and multiple and pulse supplement of magma. The hypothesis of differentiation by crystallization lacks of evidences of field and excludes by this study. On the base of the trends of formation temperatures and pressures, the characteristics of petrology, petrochemistry, geochemistry for the Fanshan complex and the characteristics of geochemistry for the rocks (or apatites), the trends of Mg/(Mg+Fe+Mn) atomic ratio of biotite and clinopyroxene in sub-rhytmic layering, and the data of oxygen, hydrogen, strontium and neodymium isotopes, this study suggests that the magma formed the Fanshan complex was formed by low degree partial melting of mantle at a low activity of H2O, and went through the differentiation at the depth of mantle, then multiply intruded and crystallized. The rhythmic layers of the First-Phase Intrusive formed by the magma fractional crystallized in two vis-a-vis ways, from the bottom and top to the centre in-situ fractional crystallization. The apatite (-magnetite) deposit of the Fanshan complex occurs in sub-rhythmic layering sequence. The the origin of the sub-rhythmic layering is substantially the origin of the Fanshan apatite (-magnetite) deposit. The magma formed the rhythmic layers of First-Phase Intrusive was rich in H2O, F and P at the later stage of its in-situ fractional crystallization. The Fanshan apatite (-magnetite) deposit was formed by this residual magma in-situ fractional crystallization. The magnetite-apatite rock was crystallized by two vis-a-vis ways at the latest stage in-situ fractional crystallization in the rhythmic layers. The result was light apatite layer below heavy the magnetite-apatite layer, formed an "inversion" phenomenon.

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苔藓植物由于具有特殊的形态结构和生物学性质而被广泛应用于环境变化和大气沉降的指示和监测,而稳定同位素(如13C、15N、34S)是辨识环境体系中物源走向以及研究植物和环境关系的可靠技术。本论文正是结合苔藓生物指示方法和稳定同位素示踪技术,开展了苔藓碳氮同位素指示环境条件和大气氮沉降的初步研究。通过不同环境条件下苔藓同位素的对比研究,揭示了苔藓碳氮同位素对环境因子和氮沉降变化的响应机制。进而应用石生苔藓碳氮元素含量和同位素,并结合光合色素含量等参数,对贵阳地区的大气氮沉降进行了详细研究,深化了苔藓同位素方法在环境监测和大气氮沉降研究中的应用,并为城市氮污染的防治提供了地球化学依据。获取了一些有意义的发现和创新点。 1. 不同生长条件下苔藓元素含量和同位素的变化及其意义 即使在同一地点,苔藓13C会由于水分条件和光照条件的差异而发生明显变化,而树冠对大气沉降物质的长期截留吸收会使下方苔藓氮硫含量偏低以及同位素偏负,其同位素效应还与树冠类型和树冠厚度有关。因此,应用苔藓元素含量和同位素指示区域环境和大气沉降时应尽量消除生境差异的影响,受生长条件影响或歪曲了的苔藓指示信息可能导致在解释环境变化和大气沉降时得出错误的结论,相对而言,开阔地的石生苔藓是较可靠的指示工具。利用同位素方法探讨苔藓记录信息的差异是本研究的创新点之一,目前国内外尚无相关的报道,这深化了苔藓碳氮同位素对环境条件和大气输入响应机制的认识,同时还为苔藓同位素研究大气沉降提供了采样指导。 2. 不同地区苔藓新老组织碳氮含量和同位素组成特征 贵阳市区苔藓碳含量高于贡嘎山地区,而13C明显偏负,表明城市苔藓受人为CO2排放的影响,而非污染区苔藓13C能够响应海拔和年均温度的差异。贵阳市区苔藓氮含量较高反映其氮沉降高于贡嘎山地区,明显偏负的15N值主要指示了城市废水氨释放的影响。不同地区苔藓新生组织的碳氮含量总体高于衰老组织,但同位素没有明显变化,反映了生理功能的衰退和部分元素向新生组织迁移会导致老组织碳氮含量降低,但不会明显改变其碳氮同位素记录,新组织氮含量较可靠地反映了氮沉降的水平(贵阳市约为30.18 kg/ha/yr,贡嘎山地区约为8.46 kg/ha/yr)。本研究扩展了苔藓同位素对不同地区环境因子和氮沉降差异的响应状况,并首次探讨了苔藓衰老对其碳氮含量和同位素记录的影响,为深入理解非维管植物衰老过程的碳氮同位素分馏奠定基础。 3. 贵阳地区大气氮沉降的空间分布 根据大气氮沉降和苔藓氮含量之间的定量关系(y=0.052x+0.7325),可以利用石生苔藓氮含量(0.85% ~ 2.97%)计算贵阳地区的大气氮沉降。贵阳地区的氮沉降(0.91 kg/ha/yr ~ 44.69 kg/ha/yr)总体已经超过最易受影响的陆地生态系统的氮沉降负荷值(5 kg/ha/yr ~ 10 kg/ha/yr),市区氮沉降平均值(29.21±6.17 kg/ha/yr)与前期监测值(30.18kg/ha/yr)基本一致,高于酸性针叶林和落叶林的氮沉降负荷值(15 kg/ha/yr ~ 20 kg/ha/yr)。而农村地区氮沉降平均值(14.31±5.11 kg/ha/yr)与贵州农村地区铵沉降的平均值(14.3 kg/ha/yr)吻合。本研究首次根据石生苔藓氮含量量化了氮沉降的水平和空间分布,对大气氮沉降生态环境影响的评价以及喀斯特地区脆弱生态系统的保护具有重要意义。 4. 贵阳地区大气氮沉降的主要来源和主要形态 贵阳地区石生苔藓15N值(-12.50‰ ~ -1.39‰)呈明显的双峰分布模式(-12‰ ~ -6‰和-5‰ ~ -2‰),表明该地区的氮沉降存在两个主要来源。市区明显偏负的苔藓15N值(平均-8.87±1.65‰,<5km; -8.59±2.28‰,5 km ~ 10km)主要反映城市废水和人畜排泄物NH3的影响,而往外到农村较高的苔藓15N值(平均-3.83±0.82‰ ~ -2.48±0.95‰,>15km)主要指示了农业NH3的贡献。根据市区苔藓和雨水15N值计算,市区氮沉降中铵态氮的贡献约占76%,硝态氮约为23%,贵阳地区的氮沉降以铵沉降为主。本研究首次发现了以铵沉降为主的城市地区苔藓15N值市区偏负、农村偏正的变化规律,这与氮沉降以硝态氮为主的城市苔藓15N变化(市区偏正、农村偏负)相反。此外,根据苔藓15N随大气沉降中铵态氮和硝态氮比值的变化规律,贵阳地区苔藓氮含量和15N的变化主要由两种不同铵源(城市铵和农业铵)的变化所控制,贵阳苔藓氮含量和15N的空间变化可以进一步作为铵沉降变化的证据。 5. 贵阳地区主要大气氮源(铵)的沉降机制与模式 贵阳市区往外石生苔藓氮含量随离市中心的距离呈指数降低(y=1.5e-0.13x+1.26),而15N值随距离对数升高(y=2.54Ln(x)-12.23),揭示了城市来源的铵沉降从市区往外随距离指数降低,其分布模式为点源模式,贵阳市区可被视为贵阳地区的一个点状氨源。而农村地区苔藓氮含量不随距离而变化、15N值不存在明显差异,反映了农业氨的面源分布模式。通过极限法计算苔藓氮含量和15N随距离变化的函数,氮沉降在离市中心17.2km以内以城市铵为主,以外以农业铵为主,城市铵的影响范围总体小于41km,城市铵随离市中心距离的变化关系为y=56.272e-0.116x-0.481。此外,贵阳市区往外不同方向的苔藓氮含量和15N随距离的变化梯度存在差异,表明城市铵向周边不同方向的传输具有非均一性,这主要与不同方向的地形条件、地表植被状况、风向、城市化程度等差异有关。本研究首次通过苔藓监测证实以铵沉降为主的城市,城市铵沉降的分布呈点源模式,并通过苔藓氮含量和15N的变化得出了城市铵的定量分布、沉降机制和影响因素。 6. 贵阳地区石生苔藓碳含量和13C值的变化及其意义 贵阳地区石生苔藓碳含量(34.47% ~ 52.76%)从市区到农村随距离指数降低(y=9.206e-0.042x+38.024),并与氮含量存在正相关关系,表明大气氮输入具有增加苔藓碳含量的作用。苔藓13C值(-30.69‰ ~ -26.96‰)从市区到农村随距离逐渐升高(y=0.674Ln(x)-30.03),反映了城市人为CO2的影响逐渐减小。此外,苔藓13C随碳氮含量增加而降低,碳氮同位素存在正相关关系,反映了石生苔藓光合作用与氮素吸收相互制约,市区较高的氮沉降或铵沉降增强了苔藓光合作用和碳代谢,使苔藓在固碳过程中发生更大的13C分馏。本研究首次发现了城市地区较高的氮沉降能够促进石生苔藓光合固碳能力,苔藓13C值能够指示城市人为CO2的影响以及氮沉降的生物效应。 7.其它创新之处 为深入认识城市地区氮沉降的变化及其生物响应,本研究还对石生苔藓光合色素含量进行了分析,首次探讨了石生苔藓光合生理参数和碳氮含量、碳氮同位素之间的关系。市区苔藓光合色素含量高于农村地区,叶绿素含量与碳氮含量存在正相关关系,表明光合色素分析可以反映环境胁迫状况、苔藓固碳能力和氮素营养状况。叶绿素含量与13C值呈负相关关系指示了氮沉降增强石生苔藓光合作用的机制。

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近年来铜、锌同位素地球化学研究已经进入了快速发展时期。作为新兴的同位素技术手段,铜锌同位素工具已普遍应用于地球化学、矿床学、古海洋学和生物学等多种领域,然而铜、锌同位素在湖泊生态系统中的研究却相对较少。湖泊生态系统中,重金属的迁移、循环与转化一直是地球科学家们关注的焦点,但研究手段仅局限于含量与形态的测定。因此本论文旨在通过对湖泊生态系统中铜、锌同位素的研究,揭示影响铜、锌同位素组成的主要因素,为铜、锌同位素成为湖泊系统中新的重金属示踪工具奠定基础。 本论文通过一系列条件实验,确定了用于MC-ICP-MS测定环境样品中铜、锌同位素时最佳的化学分离条件。随后选取红枫湖和阿哈湖为主要研究对象,用此实验流程对湖泊水体及其主要支流悬浮物中的铜、锌同位素的季节及剖面变化进行了初步研究。除此之外,对水体中重金属如Cu、Zn、Mn、Ni、Co、Cr、Cd和Pb的形态分布特征及物质循环进行了研究。主要得出以下几点认识: 1、环境样品中铜锌的最佳分离条件是,采用AG MP-1(100-200目)阴离子交换树脂,分别以7 mol/L HCl + 0.001% H2O2,2 mol/L HCl+ 0.001% H2O2,0.5 mol/L HNO3作为淋洗液,并分别在适当的体积接收淋洗液,可以有效地分离沉积物、植物和悬浮物等样品中的铜和锌。化学分离过程中回收率接近100%,同位素比值的变化均在误差范围以内。 2、红枫湖、阿哈湖水体及主要支流悬浮物和红枫湖生物样品中的δ65Cu分布范围为-2.64‰~1.11‰,可达到3.75‰的变化。红枫湖夏季水体悬浮物的δ65Cu变化为-0.08‰~0.25‰,入湖河流水体悬浮物δ65Cu的变化范围为0.13‰~ 1.11‰;阿哈湖夏季水体悬浮物δ65Cu的变化范围为-0.62‰~0.37‰,入湖河流水体悬浮物δ65Cu的变化范围为-1.08‰~0.60‰。两湖冬季水体悬浮物的δ65Cu值均较负。红枫湖生物样品中δ65Cu较负(-1.54‰~ 0.03‰)。 红枫湖水体悬浮物中δ65Cu的随水深的变化趋势主要受到藻类吸收作用的控制,而阿哈湖δ65Cu的随水深的变化趋势主要受到其物源的控制。说明在贫营养化湖泊中,铜同位素组成可以示踪物源;而在富营养化湖泊中,铜同位素组成则可以示踪生物活动。同时水温的垂直变化也可能是其影响因素之一。 3、红枫湖水体及其主要支流水体悬浮物中的δ66Zn变化范围分别为-0.29‰~0.26‰和-0.04‰~0.48‰,阿哈湖水体及其主要支流水体悬浮物中的δ66Zn变化范围分别为-0.18‰~0.27‰和-0.17‰~0.46‰,均表现出支流中的锌同位素组成较重的趋势。而生物样品中的δ66Zn变化范围较大,为-0.35‰~0.57‰。说明湖泊生态系统中各端元的锌同位素组成存在明显差异。 红枫湖夏季δ66Zn随着湖水深度的变化,与Chla(叶绿素)呈极显著的正相关(R=0.97)。说明锌同位素组成与藻类生物量有一定的响应关系,主要是藻类对锌的有机吸附或是吸收过程改变了锌同位素组成。阿哈湖的锌同位素组成主要受到其源区的控制作用,从而可利用锌同位素示踪源区;此外,红枫湖和阿哈湖悬浮物中的锌同位素比值均表现出夏季小于冬季,说明大气的干湿沉降可能是一个较负的锌同位素源。生物样品中的δ66Zn变化范围较大,说明由于生物作用过程导致的锌同位素分馏大于非生物过程。 4、红枫湖重金属Mn、Ni、Co、Cr、Cd和Pb的含量在南湖高于北湖,主要是羊昌湖的输入所导致;重金属入湖通量的季节性变化,直接导致了重金属含量的季节性变化。沉积物-水界面在冬夏季节,由于“富氧”和“贫氧”状态的改变,导致了溶解态Mn、Ni和Cr的季节性变化;水粒相互作用过程中,溶解有机碳(DOC)、氧化铁胶体、氧化锰胶体和水生藻类的生长繁殖,影响了重金属不同结合形态的变化。

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锂的两个同位素(6Li和7Li)之间相对大的质量差导致它们在自然界的分馏强烈,仅在表生环境就达到了35‰。因而,作为一种有效的示踪剂被广泛地应用于研究宇宙事件、洋壳蚀变及海底热液活动、板块活动、壳幔演化以及示踪卤水来源等地球化学过程。近年来则以大陆风化过程的锂同位素地球化学研究为热点,主要研究方向包括流域尺度大空间范围的总体研究、风化壳剖面的精细研究以及实验室的模拟研究,均涉及水/岩作用过程的锂同位素分馏机理研究。但是,现有的研究结果有的需要进一步论证,有的相互之间存在矛盾,还有部分结论不能自圆其说。 因此,本项论文工作以地表环境过程的锂同位素地球化学研究为切入点,选择长江水系干流和主要支流的地表水、悬浮物和沉积物为研究对象。在低含量样品锂同位素分析方法研究和完善的基础上,就河流体系锂的来源、流域体系的锂同位素组成变化特征及其主要受控因素等方面开展探索性研究。 通过以上研究,本论文得出以下几点认识: 1、采用单一的阳离子树脂柱分离、提纯样品锂,MC-ICP-MS测定其同位素组成。其分析结果的准确度和精确度可以达到现阶段报道的最高水平。海水的锂同位素组成为+31.3±1.0‰(2σ)与前人测定结果的平均值(+31.2‰)接近;样品分析误差约为0.5‰(2σ),与TIMS的分析结果相似。 2、长江水系河水以富含HCO3-、Ca2+为主要特征,两者分别占阴、阳离子总量的70%和50%;其中,以Na+、Cl-含量的变化最大。长江河水的主要离子组成主要受流域岩石风化作用影响,蒸发结晶作用只在少数点起次要作用,而大气沉降的输入十分微弱。岩石风化作用以碳酸盐岩风化的影响最为显著,蒸发盐岩和硅酸岩的影响较小,仅限于长江流域的局部地区。 3、长江水系悬浮物的锂含量及δ7Li值变化较小,分别为41 µg/g~92 µg/g和-4.7‰~+0.7‰。沉积物的锂含量在13.26 µg/g~46.32 µg/g之间,略低于悬浮物的锂含量,而δ7Li较高,在+0.9‰和+9.1‰之间变化。悬浮物和沉积物的锂含量与Al2O3/SiO2、Fe2O3/SiO2、MnO/SiO2及K2O/SiO2等比值之间存在明显的正相关关系,与δ7Li值存在一定的负相关关系,主要表现为粘土矿物对锂的吸附作用,尤其是6Li。 4、长江水系河水的锂含量在1.04 µg/L和31.72 µg/L之间,平均为8.87 µg/L,呈现出从上游至下游逐渐降低的趋势,最高值出现在长江上游的攀枝花段(CJ1)。其锂同位素组成变化也较大,δ7Li值在+7.6‰和+28.1‰之间,但是却呈现出与锂含量变化相反的特征,即从上游至下游逐渐增加,最小值出现在长江上游的攀枝花段(CJ1)。 5、长江干流水体的锂摩尔浓度的倒数(1/Li)和δ7Li值之间存在明显的正相关关系,可能是两个端员组分混合的结果。综合考虑雨水、人为输入和碳酸盐岩对长江干流河水的贡献后,我们认为长江干流河水的锂应该是来自于流域岩石风化的贡献,即蒸发盐岩的溶解和硅酸岩的风化,两者对长江河水锂的贡献在78%和99%之间。 6、悬浮物总是比相应水体富集6Li,导致两者之间的锂同位素分馏明显。悬浮物和河水之间的锂同位素分馏系数(α矿物-流体)在0.976和0.993之间比变化,落在不同粘土矿物吸附产生的分馏范围内。长江上游地区的α矿物-流体落在室温下水铝矿和蒙脱石对锂吸附产生的分馏范围内,下游地区的α矿物-流体则与蛭石和高岭石对水体锂的吸附分馏范围内。除此之外,α矿物-流体还与悬浮物的量密切相关,尤其是在河水进入三峡库区之前。这种相关性同样是粘土矿物对6Li的优先吸附引起的。

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了解过去是认识现在和预测未来的基础。晚全新世是PAGES研究的目标时段之一。寻找和解译最近2000年连续、高分辨率自然记录是古气候研究的热点与难点。本项研究有针对性地选择程海、草海和青海湖开展湖泊沉积物环境记录的精细研究,结合14C、210Pb和137Cs定年,系统探讨了碳酸盐碳氧同位素、纤维素碳氧同位素、有机质碳同位素以及介形虫壳体Li/Ca比值指标的古环境指示意义。 通过研究,本论文取得了如下成果和新的认识: 1. 建立了一套有效的四阶段湖泊沉积物有机质纤维素提取方法(5%NaOH碱洗、5%HCl酸洗、亚氯酸钠和冰醋酸混合溶液漂白以及17.5%NaOH碱洗),红外光谱鉴定提取物为纯的α-纤维素,表明该实验方法是可行的,为今后广泛开展湖泊沉积物纤维素稳定同位素研究打下了坚实基础。 2. 多指标综合辨识了程海和草海沉积物碳酸盐主要是自生碳酸盐。程海和草海沉积物有机质C/N比值结合有机质碳同位素结果表明两湖的有机质分别源于水生植物藻类和大型水草。程海和草海沉积物碳酸盐含量主要反映了湖区温度的变化。 3. 程海、草海沉积物碳酸盐与青海湖沉积物介形虫壳体氧同位素组成均反映了湖区降水/蒸发比。降水/蒸发比大的湿润期,碳酸盐δ18O值小;降水/蒸发比小的干旱期,碳酸盐δ18O值大。程海沉积物碳酸盐碳同位素组成影响因素复杂,除了受大气与湖水之间的CO2交换影响外,还受水生植物光合/吸收作用的影响;草海沉积物碳酸盐碳同位素组成更大的变化范围,反映了湖区水生植物光合/吸收作用的影响,其异常的正值可能指示了湖区细菌参与有机质碳同位素分馏过程。 4. 利用草海沉积物有机质纤维素氧同位素定量恢复了湖水氧同位素组成变化。在此基础上,结合碳酸盐氧同位素组成初步恢复了草海地区过去500年来温度变化历史:草海地区在过去500年明显存在四个冷期,包括1550-1610年,1670-1730年,1770-1870年和1890-1920年冷期,其中前三个发生在传统意义上的现代小冰期时段。与其它记录研究结果的一致性表明纤维素氧同位素结合碳酸盐氧同位素是恢复古温度变化的最有效途径之一,同时也为现代小冰期在中国西南地区的存在提供了湖泊沉积学方面的证据。 5. 不同类型水生植物湖泊,湖泊沉积物有机质δ13C值对湖泊初级生产力变化的响应过程不同。大型水草为主的湖泊(草海),其沉积物有机质δ13C值随湖泊生产力的增大呈现增加的变化趋势;藻类为主的湖泊(程海),其沉积物有机质δ13C随湖泊生产力的增大呈现减小的变化趋势,藻类易降解是导致δ13C值随湖泊生产力的增大呈现减小变化趋势的主要原因。 6. 程海沉积物碳酸盐和有机质碳同位素组成的正相关变化以及草海沉积物碳酸盐和有机质碳同位素组成的负相关变化.表明湖泊生产力变化并不是导致碳酸盐和有机质碳同位素正相关变化的主要原因,湖泊水生植物类型以及湖泊大小均起着重要作用。湖泊沉积物碳酸盐与有机质之间的碳同位素分馏(△δ13C)是一种有效的湖泊生产力指示剂,即使是在有微生物参与有机质碳同位素分馏过程的草海,△δ13C值也反映了湖泊生产力的变化过程。 7. 青海湖沉积物单一种属介形虫壳体胖真星介(Eucypris inflata)Li/Ca比值与气象记录以及邻近地区都兰和祁连山树轮宽度指数恢复的古温度变化序列的对比研究揭示,介形虫壳体Li/Ca比值与温度呈明显的负相关变化(Li/Ca比值高,温度低;Li/Ca比值低,温度高),表明介形虫壳体Li/Ca比值是一种有效的古温度代用指标。 8. 青海湖沉积物单一种属介形虫壳体胖真星介(Eucypris inflata)Li/Ca比值、氧同位素与反映太阳活动的大气14C含量和冰芯10Be含量的一致性变化表明青海湖地区温度和降雨量的同步变化主要受太阳活动控制。

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Mountaintop mining (MTM) is the primary procedure for surface coal exploration within the central Appalachian region of the eastern United States, and it is known to contaminate streams in local watersheds. In this study, we measured the chemical and isotopic compositions of water samples from MTM-impacted tributaries and streams in the Mud River watershed in West Virginia. We systematically document the isotopic compositions of three major constituents: sulfur isotopes in sulfate (δ(34)SSO4), carbon isotopes in dissolved inorganic carbon (δ(13)CDIC), and strontium isotopes ((87)Sr/(86)Sr). The data show that δ(34)SSO4, δ(13)CDIC, Sr/Ca, and (87)Sr/(86)Sr measured in saline- and selenium-rich MTM impacted tributaries are distinguishable from those of the surface water upstream of mining impacts. These tracers can therefore be used to delineate and quantify the impact of MTM in watersheds. High Sr/Ca and low (87)Sr/(86)Sr characterize tributaries that originated from active MTM areas, while tributaries from reclaimed MTM areas had low Sr/Ca and high (87)Sr/(86)Sr. Leaching experiments of rocks from the watershed show that pyrite oxidation and carbonate dissolution control the solute chemistry with distinct (87)Sr/(86)Sr ratios characterizing different rock sources. We propose that MTM operations that access the deeper Kanawha Formation generate residual mined rocks in valley fills from which effluents with distinctive (87)Sr/(86)Sr and Sr/Ca imprints affect the quality of the Appalachian watersheds.

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Two-color above threshold ionization of helium and xenon has been used to analyze the synchronization between individual pulses of the femtosecond extreme ultraviolet (XUV) free electron laser in Hamburg and an independent intense 120 fs mode-locked Ti:sapphire laser. Characteristic sidebands appear in the photoelectron spectra when the two pulses overlap spatially and temporally. The cross-correlation curve points to a 250 fs rms jitter between the two sources at the experiment. A more precise determination of the temporal fluctuation between the XUV and infrared pulses is obtained through the analysis of the single-shot sideband intensities. ©2007 American Institute of Physics

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We report on the observation of fast hydrogen atoms in a capacitively coupled RF reactor by optical emission spectroscopy. For the analysis we use the prominent H-alpha emission line of atomic hydrogen in combination with other lines from molecular hydrogen and argon. Several chaxacteristic emission structures can be identified. One of these structures is related to fast hydrogen atoms traveling from the surface of the powered electrode to the plasma bulk. From the appearance time within the RF period we conclude that this feature originates from ion bombardment of the electrode surface. Measured pressure dependencies and a simple model for the ion dynamics support this assumption.

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Background: After a volcano erupts, a lake may form in the cooled crater and become an isolated aquatic ecosystem. This makes fishes in crater lakes informative for understanding sympatric evolution and ecological diversification in barren environments. From a geological and limnological perspective, such research offers insight about the process of crater lake ecosystem establishment and speciation. In the present study we use genetic and coalescence approaches to infer the colonization history of Midas cichlid fishes (Amphilophus cf. citrinellus) that inhabit a very young crater lake in Nicaragua-the ca. 1800 year-old Lake Apoyeque. This lake holds two sympatric, endemic morphs of Midas cichlid: one with large, hypertrophied lips (~20% of the total population) and another with thin lips. Here we test the associated ecological, morphological and genetic diversification of these two morphs and their potential to represent incipient speciation.
Results: Gene coalescence analyses [11 microsatellite loci and mitochondrial DNA (mtDNA) sequences] suggest that crater lake Apoyeque was colonized in a single event from the large neighbouring great lake Managua only about 100 years ago. This founding in historic times is also reflected in the extremely low nuclear and mitochondrial genetic diversity in Apoyeque. We found that sympatric adult thin- and thick-lipped fishes occupy distinct ecological trophic niches. Diet, body shape, head width, pharyngeal jaw size and shape and stable isotope values all differ significantly between the two lip-morphs. The eco-morphological features pharyngeal jaw shape, body shape, stomach contents and stable isotopes (d15N) all show a bimodal distribution of traits, which is compatible with the expectations of an initial stage of ecological speciation under disruptive selection. Genetic differentiation between the thin- and thick-lipped population is weak at mtDNA sequence (FST = 0.018) and absent at nuclear microsatellite loci (FST < 0.001).
Conclusions: This study provides empirical evidence of eco-morphological differentiation occurring very quickly after the colonization of a new and vacant habitat. Exceptionally low levels of neutral genetic diversity and inference from coalescence indicates that the Midas cichlid population in Apoyeque is much younger (ca. 100 years or generations old) than the crater itself (ca. 1 800 years old). This suggests either that the crater remained empty for many hundreds of years after its formation or that remnant volcanic activity prevented the establishment of a stable fish population during the early life of the crater lake. Based on our findings of eco-morphological variation in the Apoyeque Midas cichlids, and known patterns of adaptation in Midas cichlids in general, we suggest that this population may be in a very early stage of speciation (incipient species), promoted by disruptive selection and ecological diversification.

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We present results of experiments studying the efficiency of high harmonic generation from a gas target using the TITANIA krypton fluoride laser at the Rutherford Appleton Laboratory. The variation of harmonic yield for the 7th to 13th harmonics (355-191 Angstrom) is studied as a function of the backing pressure of a solenoid valve gas jet and of the axial position of the laser focus relative to the centre of the gas jet nozzle. Harmonic energies up to 1 mu J were produced in helium and neon targets from laser energies of approximately 200 mJ. This corresponds to absolute conversion efficiencies of up to 5 x 10(-6).

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The use of atmospheric pressure nonthermal plasma represents an interesting and novel approach for the decontamination of surfaces colonized with microbial biofilms that exhibit enhanced tolerance to antimicrobial challenge. In this study, the influence of an atmospheric pressure nonthermal plasma jet, operated in a helium and oxygen gas mixture under ambient pressure, was evaluated against biofilms of Bacillus cereus,Staphylococcus aureus,Escherichia coli and Pseudomonas aeruginosa. Within <4 min of plasma exposure, complete eradication of the two Gram-positive bacterial biofilms was achieved. Although Gram-negative biofilms required longer treatment time, their complete eradication was still possible with 10 min of exposure. Whilst this study provides useful proof of concept data on the use of atmospheric pressure plasmas for the eradication of bacterial biofilms in vitro, it also demonstrates the critical need for improved understanding of the mechanisms and kinetics related to such a potentially significant approach. © 2012 Federation of European Microbiological Societies.