998 resultados para Aragonite stalagmite


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An intrinsic exposed core optical fiber sensor (IECOFS) made from fused silica was used to monitor the crystallization of calcium carbonate (CaCO3) and CaCO3/calcium sulfate (CaSO4) composite at 100 and 120 °C in the absence and presence of low-molar-mass (Mn ≤ 2000) poly(acrylic acid) (PAA) with different end groups. The IECOFS responded only to deposition and growth processes on the fiber surface rather than changes occurring in the bulk of the solution. Hexyl isobutyrate-terminated PAA (Mn = 1400) and hexadecyl isobutyrate-terminated PAA (Mn = 1700) were the most effective species in preventing CaCO3 deposition. Phase transformation from vaterite to aragonite/calcite decreased with increasing hydrophobicity of the PAA end group. Low-molar-mass PAA at 10 ppm showed very significant inhibition of CaCO3/CaSO4 composite formation for all end groups investigated.

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Nacre, or mother-of-pearl, is a kind of composites of aragonite platelets sandwiched between organic materials. Its excellent mechanical properties are thought to stem from the micro architecture that is traditionally described as a "brick and mortar" arrangement. In this paper, a new microstructure, referred to as mineral bridge in the biomineralization, is directly observed in the organic matrix layers (mortar) of nacre. This is an indication that the organic matrix layer of nacre should be treated as a three-dimensional interface and the micro architecture of nacre ought to be considered as a "brick-bridge-mortar" structure rather than the traditional one. Experiments and analyses show that the mineral bridges not only improve the mechanical properties of the organic matrix layers but also play an important role in the pattern of the crack extension in nacre.

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Stable isotope geochemistry is a valuable toolkit for addressing a broad range of problems in the geosciences. Recent technical advances provide information that was previously unattainable or provide unprecedented precision and accuracy. Two such techniques are site-specific stable isotope mass spectrometry and clumped isotope thermometry. In this thesis, I use site-specific isotope and clumped isotope data to explore natural gas development and carbonate reaction kinetics. In the first chapter, I develop an equilibrium thermodynamics model to calculate equilibrium constants for isotope exchange reactions in small organic molecules. This equilibrium data provides a framework for interpreting the more complex data in the later chapters. In the second chapter, I demonstrate a method for measuring site-specific carbon isotopes in propane using high-resolution gas source mass spectrometry. This method relies on the characteristic fragments created during electron ionization, in which I measure the relative isotopic enrichment of separate parts of the molecule. My technique will be applied to a range of organic compounds in the future. For the third chapter, I use this technique to explore diffusion, mixing, and other natural processes in natural gas basins. As time progresses and the mixture matures, different components like kerogen and oil contribute to the propane in a natural gas sample. Each component imparts a distinct fingerprint on the site-specific isotope distribution within propane that I can observe to understand the source composition and maturation of the basin. Finally, in Chapter Four, I study the reaction kinetics of clumped isotopes in aragonite. Despite its frequent use as a clumped isotope thermometer, the aragonite blocking temperature is not known. Using laboratory heating experiments, I determine that the aragonite clumped isotope thermometer has a blocking temperature of 50-100°C. I compare this result to natural samples from the San Juan Islands that exhibit a maximum clumped isotope temperature that matches this blocking temperature. This thesis presents a framework for measuring site-specific carbon isotopes in organic molecules and new constraints on aragonite reaction kinetics. This study represents the foundation of a future generation of geochemical tools for the study of complex geologic systems.

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A decade-long time series recorded in southern Monterey Bay, California demonstrates that the shallow, near-shore environment (17 m depth) is regularly inundated with pulses of cold, hypoxic and low pH water. During these episodes, oxygen can drop to biologically threatening levels, and pH levels were lower than expected. Weekly water chemistry monitoring revealed that the saturation state of aragonite (the more soluble form of calcium carbonate) was often below saturation and had a moderate positive relationship with pH, however, analytical and human error could be high. Pulses of hypoxia and low pH water with the greatest intensity arise at the onset of the spring upwelling season, and fluctuations are strongly semidurnal (tidal) and diurnal. Arrival of cold, hypoxic water on the inner shelf typically occurs 3 days after the arrival of a strong upwelling event and appears to be driven by upwelling modulated by internal tidal fluctuations. I found no relationship between the timing of low-oxygen events and the diel solar cycle nor with terrestrial nutrient input. These observations are consistent with advection of hypoxic water from the deep, offshore environment where water masses experience a general decline of temperature, oxygen and pH with depth, and inconsistent with biochemical forcing. Comparisons with concurrent temperature and oxygen time series taken ~20 km away at the head of the Monterey Canyon show similar patterns but even more intense hypoxic events due to stronger semidiurnal forcing there. Analysis of the durations of exposure to low oxygen levels establishes a framework for assessing the ecological relevance of these events. Increasing oceanic hypoxia and acidification of both surface and deep waters may increase the number, intensity, duration and spatial extent of future intrusions along the Pacific coast. Evaluation of the resiliency of nearshore ecosystems such as kelp forests, rocky reefs and sandy habitats, will require consideration of these events.

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Corais pétreos são formadores de recifes. Por secretarem carbonato de cálcio pela base de seus pólipos, esses corais zooxantelados formam um exoesqueleto, composto geralmente por cristais de aragonita. Os padrões de crescimento coralinos variam desde a escala sazonal a centenária e podem ser caracterizados pela medida da taxa de crescimento, a variabilidade dos isótopos estáveis de oxigênio e carbono e pelas razões elementares Sr/Ca, Mg/Ca, U/Ca, Cd/Ca, Ra/Ca (entre outras) em seu esqueleto. Em um contexto global, os recifes cumprem importante papel como sumidouros de carbono atmosférico. Diante das evidências de um oceano mais quente na era moderna, a temperatura da superfície do mar (TSM) tem sido considerada um importante fator de controle da calcificação e crescimento coralino. Geralmente, a calcificação tende a aumentar com a elevação da TSM dentro de uma estreita faixa aceitável para o funcionamento pleno do metabolismo coralino. Neste trabalho, desenvolveu-se uma re-análise das taxas de crescimento de testemunhos de corais amostrados na costa brasileira (Salvador-Ba - Baía de Todos os Santos, Parque Nacional Marinho dos Abrolhos-Ba e Armação dos Búzios-RJ) empregando-se uma combinação de bandas de crescimento (alta e baixa densidades) auxiliado pelo método de luminescência e datação por radioisótopos de U e Th. As diferenças nas cronologias para os dois métodos variou de 1 ano para o caso de Abrolhos até 7,4 anos para Búzios (em seções específicas do testemunho). Foram analisadas variações de calcificação no esqueleto coralino e interpretadas à luz das razões Sr/Ca e U/Ca (ambos próxies da TSM), séries climáticas de AMO e PDO, e pH pelágico oceânico. Identificamos uma diminuição na taxa de calcificação do exoesqueleto no tempo estudado na amostra de Salvador de 0,4 g/cm2, e um aumento em Abrolhos de 0,4 g/cm2 e Búzios 0,3 g/cm2, exceto nos anos de 1950 ao final de 1980 e de 1910 ao final de 1930, respectivamente. Uma microtomografia de raio-X foi empregada para determinar micro-estruturas coralinas, sendo os parâmetros mais relevantes a microporosidade e a anisotropia. Para Abrolhos e Búzios, foi identificado um aumento na porosidade total do exoesqueleto, principalmente no começo de 1940 até o fim da década de 1980 e entre 1890 a 1930 respectivamente. Notou-se forte associação entre a redução do padrão de calcificação com o aumento da porosidade. Os testemunhos da espécie Siderastrea stellata coletados em Abrolhos e Búzios mostraram alta associação das razoes Sr/Ca e U/Ca com a taxa de calcificação, caracterizando uma resposta similar a de outros autores para a Grande Barreira na Austrália (DE'ATH et al., 2009) e para a região central do Mar Vermelho (CANTIN et al., 2010). Em relação as razões Ba/Ca, Salvador e Abrolhos evidenciaram variáveis que contribuíram para este aumento como a forçante de produção de petróleo e aumento populacional (economia), e TSM (oceano). Para Búzios, a TSM (oceano), produção de petróleo, aumento populacional e NDVI (economia). Após os anos de 1990, o impacto dos fatores econômicos, além das variáveis oceânicas respondem mais significativamente o aumento da razão Ba/Ca em todos os sítios quase que concomitantemente na costa brasileira.

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EXTRACT (SEE PDF FOR FULL ABSTRACT): Chemical isolation of lattice-bound trace elements in marine carbonates has opened new windows to paleoceanographic study. In a modern context at the Galapagos Islands, oceanic upwelling variability is mirrored by changes in the Cd content of reef-building corals. This association derives from cadmium's nutrient-like distribution in the water column and its ability to substitute for calcium in the aragonite lattice of corals. Given corals of sufficient age, it is thus possible to reconstruct near-term ENSO-related changes in surface waters of the eastern Equatorial Pacific on annual and sub-annual timescales.

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The primary objective of this study was to predict the distribution of mesophotic hard corals in the Au‘au Channel in the Main Hawaiian Islands (MHI). Mesophotic hard corals are light-dependent corals adapted to the low light conditions at approximately 30 to 150 m in depth. Several physical factors potentially influence their spatial distribution, including aragonite saturation, alkalinity, pH, currents, water temperature, hard substrate availability and the availability of light at depth. Mesophotic corals and mesophotic coral ecosystems (MCEs) have increasingly been the subject of scientific study because they are being threatened by a growing number of anthropogenic stressors. They are the focus of this spatial modeling effort because the Hawaiian Islands Humpback Whale National Marine Sanctuary (HIHWNMS) is exploring the expansion of its scope—beyond the protection of the North Pacific Humpback Whale (Megaptera novaeangliae)—to include the conservation and management of these ecosystem components. The present study helps to address this need by examining the distribution of mesophotic corals in the Au‘au Channel region. This area is located between the islands of Maui, Lanai, Molokai and Kahoolawe, and includes parts of the Kealaikahiki, Alalākeiki and Kalohi Channels. It is unique, not only in terms of its geology, but also in terms of its physical oceanography and local weather patterns. Several physical conditions make it an ideal place for mesophotic hard corals, including consistently good water quality and clarity because it is flushed by tidal currents semi-diurnally; it has low amounts of rainfall and sediment run-off from the nearby land; and it is largely protected from seasonally strong wind and wave energy. Combined, these oceanographic and weather conditions create patches of comparatively warm, calm, clear waters that remain relatively stable through time. Freely available Maximum Entropy modeling software (MaxEnt 3.3.3e) was used to create four separate maps of predicted habitat suitability for: (1) all mesophotic hard corals combined, (2) Leptoseris, (3) Montipora and (4) Porites genera. MaxEnt works by analyzing the distribution of environmental variables where species are present, so it can find other areas that meet all of the same environmental constraints. Several steps (Figure 0.1) were required to produce and validate four ensemble predictive models (i.e., models with 10 replicates each). Approximately 2,000 georeferenced records containing information about mesophotic coral occurrence and 34 environmental predictors describing the seafloor’s depth, vertical structure, available light, surface temperature, currents and distance from shoreline at three spatial scales were used to train MaxEnt. Fifty percent of the 1,989 records were randomly chosen and set aside to assess each model replicate’s performance using Receiver Operating Characteristic (ROC), Area Under the Curve (AUC) values. An additional 1,646 records were also randomly chosen and set aside to independently assess the predictive accuracy of the four ensemble models. Suitability thresholds for these models (denoting where corals were predicted to be present/absent) were chosen by finding where the maximum number of correctly predicted presence and absence records intersected on each ROC curve. Permutation importance and jackknife analysis were used to quantify the contribution of each environmental variable to the four ensemble models.

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Shells and shell fragments were the principal constituents of the core sediment taken from LakeMariut. Their trace metals were studied to assess their contribution to environmental adjustment. The results indicated that the shells of Biomphalaria alexandrina, Mercierella enigmatica and Melanoida tuberculate contain higher amounts of Cu and Zn than the widely distributed shells of Lucina sp. and Cerastoderma edule. The Pb contents found in different types of shells were higher than the other metals. The Cd contents found in different shell types were the most important fraction in comparison to the total Cd in the sediments of the lake. The relationship between the concentrations of trace metals and mineralogical analysis revealed that lead tended to be more concentrated in aragonite than in calcite.

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Different sizes of Frechet-type dendrons with a thiol group at the focal point were synthesized, well characterized, and used as building blocks for the preparation of self-assembled monolayers (SAMs) on metal surfaces. From the studies of the kinetic process of dendron thiol self-assembling on gold, it is shown that the dendron thiol assembling proceeds with different adsorption rates depending on the assembly time. In contrast to normal alkanethiols forming highly molecular structures on metal surfaces, the SAMs of polyether dendron form patterned surfaces with nanometer-sized features and in long-range order. It is found that the patterned stripes are closely related to the size of the dendron, and the patterned stripes can be improved by thermal annealing.

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The partitioning of Y and Ho between CaCO3 (calcite and aragonite respectively) and seawater was experimentally investigated at 25 degrees C and I atm. Both Y and Ho were observed to be strongly partitioned into the overgrowths of calcite or aragonite. Their partition coefficients, D-Y and D-Ho, were determined to be similar to 520-1400 and similar to 700-1900 in calcite, similar to 1200-2400 and similar to 2400-4300 in aragonite, respectively. Y fractionates from Ho during the coprecipitation with either calcite or aragonite. Within our experimental conditions, the fractionation factor, k = D-Y/D-Ho, was determined to be similar to 0.62-0.77 in calcite and similar to 0.50-0.57 in aragonite, respectively. The aqueous complexation of Y and Ho, which is a function of solution chemistry, probably plays an important role in both the partitioning and the fractionation. Further analyses suggest that the difference in covalency between Y and Ho associated with changes in their coordination environments is the determinant factor to the Y-Ho fractionation in the H2CO3-CaCO3 System.

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A 700-year record (1.0-1.5 a resolution) of the East Asian winter monsoon (EAWM), based on grain-size analysis and AMS(14)C dating of Core EC2005 from the inner-shelf mud wedge of the East China Sea (ECS), was compared with the Dongge stalagmite delta O-18 record during the mid-Holocene. The upper muddy section of Core EC2005 has been formed mainly by suspended sediments derived from the Changjiang (Yangtze) River mouth since 7.3 ka BP. High precipitation and a strengthened EAWM might have played key roles in the high sedimentation rate (1 324-1 986 cm/ka) between 5.9-5.2 ka BP. The EAWM strengthened when the Asian summer monsoon weakened, especially around 5 500 a BP, which corresponded to a worldwide cold event. The EAWM during the mid-Holocene shows statistically significant solar periodicities at 62 and 11 a. The 5 500 a BP cold event might be resulted from orbital forcing and changes in solar activity.

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本文主要运用稳定加液-反应系统对海水中方解石和文石形成时稀土元素的共沉淀现象进行了分析,研究了稀土元素在固-液体系中的迁移、转化和分配。进而在对其定量描述的前提下,研究了稀土元素共沉淀对各种反应条件的响应,并对共沉淀行为的机制进行了探讨。 本实验首先运用pH测试、高精度滴定分析等手段测定了实验中的一些基本参数,如[H+]、碱度和[Ca2+],根据计算结果获得了各碳酸体系要素,并以此为基础建立了5℃、15℃和25℃及pCO2=0.003atm下海水中方解石或文石的沉淀动力学方程。实验结果表明: 1)在各条件下,方解石或文石的沉淀速率(R)和其在海水中过饱和度(Ω)存在很好的线性相关性,即海相碳酸盐的沉淀动力学方程可以通过下面的基本表达式来表示:LogR=k*Log(Ω-1)+b ; 2)过高的稀土元素浓度会对文石或方解石的沉淀产生抑制作用,进而对共沉淀过程中YREEs的分异和分馏产生一定的影响。相比方解石而言,文石的沉淀动力学过程承受稀土元素的干扰能力更强; 3)不同温度下得到的方解石或文石各自的沉淀动力学方程存在明显的差异,表明这一过程受热力学因素控制。相对于方解石而言,温度对文石的沉淀动力学的影响更为显著。 与前人研究不同的是,本实验中YREEs的浓度设定在非常低的范围内,从而避免了过高浓度YREEs对方解石或文石沉淀动力学过程的干扰。在最终的反应液中,各种实验条件非常接近自然环境。有关稀土元素的共沉淀行为主要得出以下定性或定量化结论: 1)YREEs在随方解石或文石的共沉淀过程中,均发生了强烈的分异作用。在方解石实验中,稀土元素的分异系数分布曲线呈凸状分布;而在文石实验中,稀土元素的分异系数随原子序数的增加逐渐减小,遵循镧系收缩的规律。总的来说,稀土元素,尤其轻稀土元素在文石中的分异作用要强于方解石。 2)无论是方解石还是文石,沉淀速率对YREEs的分异作用都有着明显的影响。在方解石中,YREEs的分异系数随沉淀速率的增加呈一致性递减趋势;而在文石中,其分异系数对文石沉淀速率有着截然不同的响应:轻稀土元素(La, Ce, Nd, Sm, Eu, Gd)的分异系数随文石沉淀速率的增加而下降,而重稀土元素(Ho, Y, Tm, Yb , Lu)的分异系数则随文石沉淀速率的增加呈上升趋势。 3)在方解石中YREEs的分异系数之间存在非常好的相互关系,表明这些元素是以成比例的方式参与共沉淀。整个谱系呈现中等强度的分馏,MREE相对于LREE和HREE要更为富集;在文石中由于沉淀速率的作用不同,只有Y、Ho、Yb、Lu等元素的分异系数之间有较好的相互关系。YREEs出现了差异性的强烈分馏,在新生成沉淀中轻稀土元素相对于重稀土元素强烈富集。 4)YREEs在溶液中和碳酸盐晶体表面的碳酸根配位形式对YREEs在共沉淀过程中的分异作用极为重要,YREEs在碳酸盐晶体表面的吸附是整个谱系发生分馏效应的关键环节。对于文石来讲,晶体中有效YREE离子和Ca离子半价大小之间的相近程度是其分馏效应的关键因素;而对于方解石来说,YREEs在方解石晶格中的安置就是其分馏效应的关键控制因子,但在晶格安置中起到关键作用的是YREEs和方解石中O原子之间离子键M-O的键长,而非离子半径。 5)综合YREEs在方解石中的分异作用和分馏效应,我们认为M2(CO3)3-CaCO3和MNa(CO3)2-CaCO3是最为可能的两种固体溶液形成模式。 最为重要的是,对比我们的实验结果与前人在灰岩、叠层石、微生物成因碳酸盐等方解石质载体中的研究成果,两者之间出现了非常好的一致性。我们认为方解石质载体将是重建古海水中稀土元素相关信息的重要工具。相比之下,文石质载体不适合作为类似的载体。

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Because of the high resolution, stalagmite laminae can play an important role in the paleoclimate reconstructions. However, few investigations for the formation mechanisms of stalagmite lamilae have been done. Based on two-year observation on calcite growth rate at the drip sites, three-year monitoring of hydrodynamics, physics and chemistry of drip waters at different drip sites and the surrounding environments inside and outside the Beijing Shihua Cave, the seasonal variations of calcite growth rate are revealed and the results can be concluded as follows: 1. The drip waters inside the Cave are mostly sourced from the summer rain, and its minimal response-time to the atmospheric precipitation is less than one day. There are three types of response relationships between the precipitation and the drip rate variations: rapid response type, time-lag response type and stable response type. For rapid response type, the drip discharge is recharged through the flow routes along intensive fractures and interconnectivities; for time-lag response type, the drip discharge is recharged by double-porosity system composed of a high conductivity, low storage capability conduit network and a low-conductivity high-storage capability rock matrix under variable boundary conditions; for stable response type, the drip discharge is mainly recharged by seepage flow and base flow. 2. The observation shows that, inside the Cave, the growth rate of calcite is generally lower in rainy seasons and higher in dry seasons. During the rainy seasons, the drip water is characterized by a lower pH value, higher [Ca2+], [Mg2+], [SO42-] and electrical conductivity (EC) values. According to the calculations of saturation index of calcite (SIc), pCO2 of the drip water, as well as the synthetical analysis of other possible factors, the calcite growth rate is found to be principally influenced by the drip water saturation index of calcite (SIc). And the drip rate and pCO2 in the drip water and in the cave air play the secondly important roles in this process. The recharge mode of heavy rainfall events in the rainy seasons should probably be the main driving force that controls the physicochemical properties and calcite sediment of the drip waters. The abrupt decrease of sedimentary rate and the sharp peak of DOC in drip water in the rainy season probably forms the thin opaque (luminescent under ultraviolet radiation) layers observed in the stalagmites, whereas the relatively higher sedimentary rate in the dry seasons may be responsible for the thicker bright layers. The investigation elucidated here preliminarily reveals the formation mechanism of the stalagmite laminae in Beijing Shihua Cave.

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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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Based on chronological and climatologic analysis of many young stalagmites in Shihua Cave at Beijing and Water Cave in Benxi, Liaoning Province, this dissertation aims to discuss some key points on quantitative reconstruction of high resolution climate change from micro bands time series in young stalagmites. On chronological aspect of micro bands time series in young stalagmite, the uppermost micro bands were testified formed in the sampling year or the year before sampling from long term and in situ experiment in Shihua Cave at Beijing. Have been observed detailed under microscope, the micro bands were counted and compared with high resolution TIMS-230Th or ICP-MS U series dating, the results show that the micro bands are annual bands. The microscopic characteristics of annual bands in North China is as follows after studying lots of young stalagmites: the interface appears to be carved, and there is a light line adjacent to it, which moves back and forth slightly when adjusting the microscope slide. The cross dating of annual bands from different stalagmites is experimented in this thesis. On climatologically aspect of micro bands times series in young stalagmites, one significant problem is that the deposition trend resulting from the variation of the stalagmite shape. Various deposition trends have been discussed and corrected before climatologically analysis of micro bands series. And the whole year in situ observation and analysis of dripping water in Shihua Cave provide us new evidence for climate information reserved in stalagmites micro bands. The stalagmites in the same cave may contain different climate information due to the micro hydrological condition. The annual bands of young stalagmites collected from North China can be used to reconstruct past climate changes quantitatively. The warm season temperature (May, June, July, August) is reconstructed using two annual bands time series from Shihua Cave, Beijing, which corresponds to the warm/cool periods very well in Chinese history documents. The precipitation record of past 500 years is reconstructed using two stalagmite annual bands series from Shihua Cave, which is consistent to the dryness/wetness records derived from historical documents too.