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1.
Copper speciation in a collection of Japanese geochemical reference materials (JSO‐1, JLk‐1, JSd‐1, ‐2, ‐3 and ‐4, JMs‐1 and JMs‐2) was achieved by sequential extraction and characterised using X‐ray absorption near‐edge structure spectroscopy. In the first step of the extraction, referred to as the acid fraction, between 1% and 20% total Cu within the reference materials was extracted. Such a result is typically accounted for by absorption of Cu onto clay minerals. However, the presence of Cu sulfate (an oxidation product of chalcopyrite) was observed in some of the stream sediments affected by mining activity (JSd‐2 and JSd‐3) instead. Copper was extracted in the reducible fraction (targeting Fe hydroxide and Mn oxide) (2–49% total Cu). Between 2% and 51% Cu was extracted in the oxidised fraction (targeting sulfides and organic matter). X‐ray absorption near‐edge structure spectroscopy clarified that the reducible fraction consisted of Cu bound to Fe hydroxide, whereas the oxidised fraction was a mixture of Cu bound to humic acid (HA) and Cu sulfide. In the oxidisable fraction, chalcopyrite was the predominant species identified in JSd‐2, and Cu bound to HA was the major species identified in JSO‐1 (a soil sample).  相似文献   

2.
There is currently a lack of well‐characterised matrix‐matched reference materials (RMs) for forensic analysis of U‐rich materials at high spatial resolution. This study reports a detailed characterisation of uraninite (nominally UO2+x) from the Happy Jack Mine (UT, USA). The Happy Jack uraninite can be used as a RM for the determination of rare earth element (REE) mass fractions in nuclear materials, which provide critical information for source attribution purposes. This investigation includes powder X‐ray diffraction (pXRD) data, as well as major, minor and trace element abundances determined using a variety of micro‐analytical techniques. The chemical signature of the uraninite was investigated at the macro (cm)‐scale with micro‐X‐ray fluorescence (µXRF) mapping and at high spatial resolution (tens of micrometre scale) using electron probe microanalysis (EPMA) and laser ablation‐inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) analyses. Based on EPMA results, the uraninite is characterised by homogeneous UO2 and CaO contents of 91.57 ± 1.49% m/m (2s uncertainty) and 2.70 ± 0.38% m/m (2s), respectively. Therefore, CaO abundances were used as the internal standard when conducting LA‐ICP‐MS analyses. Overall, the major element and REE compositions are homogeneous at both the centimetre and micrometre scales, allowing this material to be used as a RM for high spatial resolution analysis of U‐rich samples.  相似文献   

3.
Reaction and deformation microfabrics provide key information to understand the thermodynamic and kinetic controls of tectono‐metamorphic processes, however, they are usually analysed in two dimensions, omitting important information regarding the third spatial dimension. We applied synchrotron‐based X‐ray microtomography to document the evolution of a pristine olivine gabbro into a deformed omphacite–garnet eclogite in four dimensions, where the 4th dimension is represented by the degree of strain. In the investigated samples, which cover a strain gradient into a shear zone from the Western Gneiss Region (Norway), we focused on the spatial transformation of garnet coronas into elongated garnet clusters with increasing strain. The microtomographic data allowed quantification of garnet volume, shape and spatial arrangement evolution with increasing strain. The microtomographic observations were combined with light microscope and backscatter electron images as well as electron microprobe (EMPA) and electron backscatter diffraction (EBSD) analysis to correlate mineral composition and orientation data with the X‐ray absorption signal of the same mineral grains. With increasing deformation, the garnet volume almost triples. In the low‐strain domain, garnet grains form a well interconnected large garnet aggregate that develops throughout the entire sample. We also observed that garnet coronas in the gabbros never completely encapsulate olivine grains. In the most highly deformed eclogites, the oblate shapes of garnet clusters reflect a deformational origin of the microfabrics. We interpret the aligned garnet aggregates to direct synkinematic fluid flow, and consequently influence the transport of dissolved chemical components. EBSD analyses reveal that garnet shows a near‐random crystal preferred orientation that testifies no evidence for crystal plasticity. There is, however evidence for minor fracturing, neo‐nucleation and overgrowth. Microprobe chemical analysis revealed that garnet compositions progressively equilibrate to eclogite facies, becoming more almandine‐rich. We interpret these observations as pointing to a mechanical disintegration of the garnet coronas during strain localization, and their rearrangement into individual garnet clusters through a combination of garnet coalescence and overgrowth while the rock was deforming.  相似文献   

4.
Speciation of Cr in geochemical reference materials was characterised by sequential extraction and X‐ray absorption near‐edge structure (XANES) spectroscopy to identify Cr(III) resulting from the reduction of pollutant Cr(VI). Sequential extraction suggested that the amount of Cr associated with an acetic acid soluble fraction was low; Cr associated with a reducible phase and an oxidisable phase was extracted at 5–10% of the total Cr concentration, and the residual phase was found to be the dominant Cr‐containing fraction. Cr speciation in soil artificially doped with Cr(VI) and sediment samples collected from highly populated and industrialised areas was different from that in naturally occurring materials. Substantial Cr was extracted as a reducible phase (15–30%) and an oxidisable phase (30–60%) for these samples. Through subsequent XANES spectroscopy analysis, the reducible phase was explained by Cr bound to Fe hydroxide, while the oxidisable phase was a mixture of Cr bound to humic substances and Cr hydroxides. That is, Cr(VI) present as a contaminant in sediments and soils was reduced to Cr(III), which then bound to Fe hydroxide and humic substances, precipitating as a hydroxide. Thus, a combination of sequential extraction and XANES spectroscopy allows for effective identification and quantification of the chemical forms of Cr in sediments and soils.  相似文献   

5.
Laser‐induced breakdown spectroscopy (LIBS) records light emitted from the decay of electrons to lower‐energy orbitals during cooling of laser‐induced ablation plasmas; the resultant spectra can be used in a variety of geoanalytical applications. Four aspects of LIBS analysis distinguish LIBS from traditional laboratory‐based analytical techniques: (i) the lack of necessary sample preparation, allowing rapid analysis of many samples, (ii) the ability to analyse both 20 to 100 μm‐diameter spots and whole rocks, (iii) the detailed chemical signature contained in a LIBS spectrum and (iv) the ability to take LIBS into the field in backpack portable instrumentation. Three case studies illustrate potential applications of LIBS in the geosciences. First, analysis of the Carrizozo basalt flow in New Mexico, USA, illustrated that LIBS spectra could discriminate between samples of similar composition within uncertainties typical of whole‐rock analysis by X‐ray fluorescence spectrometry. Second, spectra from four sets of rubies from Madagascar and Tanzania illustrate the use of LIBS and multivariate analysis to determine provenance with success rates of > 95%. This technique can also be applied to correlation of units. Finally, a chemical map of a copper ore from Butte, MT, USA, illustrates the use of spatially defined LIBS spectra to understand chemical variations within textural context.  相似文献   

6.
下庄铀矿为一花岗岩型铀矿，矿田地处湿热气候条件下，沥青铀矿普遍产于破碎带中，这种特定的产出环境致使该区沥青铀矿经受了强烈的风化，形成种类繁多、数量丰富的铀酰矿物；而我国高放废物地质处置库拟建在花岗岩体中。因此，下庄铀矿田是开展核废料氧化的天然类比研究的理想地区，并对我国的高放废物地质处置库的安全性评价有重要的指导作用。下庄铀矿田的铀酰矿物组合为铀酰氢氧化物、铀酰硅酸盐和铀酰磷酸盐，包括柱铀矿、黄钙铀矿、calciouranoite、红铀矿、富硅铀酰相、硅钙铀矿、钙铀云母和盈江铀矿等。根据它们的空间分布特征可划分成两个风化系列，即硅酸盐风化系列和磷酸盐风化系列，其共生次序分别为：沥青铀矿→铀酰氢氧化物（氧化物）→富硅铀酰相→硅钙铀矿和沥青铀矿→铀酰氢氧化物（氧化物）→钙铀云母→盈江铀矿。在该矿田中，铀酰氢氧化物是亚稳定相矿物，常常被铀酰硅酸盐或磷酸盐取代，因此，铀酰氢氧化物仅出现在少数样品中，而铀酰硅酸盐和铀酰磷酸盐矿物则非常普遍。矿田中的铀酰矿物在化学成分上以富钙为其显著特征，由于核废料地质处置库近场地下水中的Ca^2＋含量应该明显比下庄矿田地下水中的高，因此，我们预测含Ca的铀酰硅酸盐和铀酰磷酸盐矿物等热力学上的稳定物相很可能是地质处置系统中最主要的铀酰矿物，处置库内放射性核素的迁移主要是由这些矿物控制的。  相似文献   

7.
The strong spectral interference between Br‐ and Al‐induced X‐ray lines hampers the utilisation of electron probe microanalysis (EPMA) for measuring Br mass fractions in Al‐bearing minerals and glasses. Through measuring Br‐free Al‐bearing materials, we established an EPMA method to quantify the overlap from AlKα on BrLβ, which can be expressed as a linear function of the Al2O3 content. The count rate of the BrLβ peak signal was enhanced by high beam currents and long measurement times. Application of this EPMA method to Al‐ and Br‐bearing materials, such as sodalite and scapolite, and to five experimental glasses yielded Br mass fractions (in the range of 250–4000 μg g?1) that are consistent with those measured by microbeam synchrotron X‐ray fluorescence (μ‐SXRF) spectrometry. The EPMA method has an estimated detection limit of ~ 100–300 μg g?1. We propose that this method is useful for measuring Br mass fractions (hundreds to thousands of μg g?1) in Al‐bearing minerals and glasses, including those produced in Br‐doped experiments. In addition, the natural marialitic scapolite (ON70) from Mpwapwa (Tanzania) containing homogeneously distributed high mass fractions of Br (2058 ± 56 μg g?1) and Cl (1.98 ± 0.03% m/m) is an ideal reference material for future in situ analyses.  相似文献   

8.
Grain‐size distribution is a fundamental tool for interpreting sedimentary units within depositional systems. The techniques assessed in this study are commonly used to determine grain‐size distributions for sand‐dominated sediments. However, the degree of consistency and differences in interpretation when using a combination of grain‐size methods have not yet been assessed systematically for sand‐dominated fluvial sediments. Results obtained from laser diffraction, X‐ray attenuation and scanning electron microscopy grain‐size analysis techniques were compared with those obtained from the traditional sieve/hydrometer method. Scanning electron microscopy was shown to provide an inaccurate quantitative analysis of grain‐size distributions because of difficulties in obtaining representative samples for examination. The X‐ray attenuation method is unsuitable for sand‐dominated sediments because of its upper size range of only 300 μm. The consistently strong correlation between the laser diffraction results and the sieve/hydrometer results shows that these methods are comparable for sand‐dominated fluvial sediments. Provided that sample preparation is consistent, the latter two methods can be used together within a study of such sediments while maintaining a high degree of accuracy. These results indicate that data for sand‐dominated fluvial sediments gained from the long‐established sieve/hydrometer method can be compared with confidence to those obtained by modern studies using laser diffraction techniques.  相似文献   

9.
Optically stimulated luminescence (OSL) dating is widely used to date clastic deposits, including those collected by coring. X‐ray scanning of cores has become popular because of the rapidly acquired, high‐resolution information it gives about optical, radiographic and elemental variations. Additionally, X‐ray scanning is widely viewed as a non‐destructive method. However, such instruments use an intense X‐ray beam that irradiates the split core to enable both X‐radiographic and X‐ray fluorescence (XRF) analysis. This irradiation will influence the optically stimulated luminescence signal in the sediments. This study determines the radiation dose delivered to sediments in a core during an X‐ray scan, and assesses the implications for studies wishing to combine X‐ray scanning and OSL dating. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

10.
X‐ray computed microtomography is used to obtain high resolution imagery of a historical tsunami deposit in Andalusia, Spain (1755 Lisbon tsunami). The technique allows characterization of grain‐size distribution, structures, component analysis and sedimentary fabric of fine‐grained unconsolidated tsunami deposits at resolutions down to particle scale. The results are validated by comparing to data obtained using other techniques such as laser diffraction, anisotropy of magnetic susceptibility and X‐ray microfluorescence on the same deposits. Specific technical details such as sampling, scanning and image processing methods, and further improvements are addressed. The use of X‐ray computed microtomography provides new insights into the stratigraphy of the deposits and gives access to significantly more detailed view of key sedimentary features such as mudlines, rip‐up clasts, crude laminations, convolutions, floating outsized clasts and contacts between successive units. This analysis of the 1755 tsunami deposits using X‐ray computed microtomography allows the proposal of new hypotheses for the sedimentary processes forming tsunami deposits. Deposition by settling is limited and the section analysed here is dominated by a high shear stress leading to the development of traction carpets, with laminated mudlines corresponding to the basal frictional region of these carpets. The onset of the tsunami backwash is marked by a micro‐vortex resembling Kelvin–Helmoltz instabilities.  相似文献   

11.
Comparing spaceborne satellite images of Landsat‐8 Operational Land Imager (OLI) and Landsat‐7 Enhanced Thematic Mapper plus (ETM+) was undertaken to investigate the relative accuracy of mapping hydrothermal alteration minerals. The study investigated the northern part of Rabor, which contains copper mineralization occurrences, and is located in the Kerman Cenozoic magmatic assemblage (KCMA), Iran. Image processing methods of band ratio, principal component analysis (PCA), and spectral angle mapper (SAM) were used to map the distribution of hydrothermally altered rocks associated with the porphyry copper mineralization. The band ratio combination of both sensors for mapping altered areas showed similar outcomes. PCA exposed variations in the spatial distribution of hydroxyl‐bearing minerals. The representation of hydrothermal areas using OLI data was more satisfactory than when using ETM+ data. SAM analysis found similar results for mapping hydroxyl‐bearing zones. Verification of the results came through ground investigation and laboratory studies. Rock samples (n = 56) were collected to validate results using thin sections, X‐ray diffraction (XRD) and spectral analyses. Field observations and laboratory analysis revealed that phyllic and propylitic alterations dominate the alteration zones in the study area. Argillic and iron oxides/hydroxides alterations were observed to a lesser degree. The results indicate that alteration maps prepared by OLI data using PCA for visual interpretation are more suitable than those of ETM+ due to a higher radiometric resolution and lower interference between vegetation and altered areas. As the spectral bandwidth of ETM+ band 7 covers absorption feature of propylitic alteration, better mapping of propylitic alterations is achieved using ETM+ data.  相似文献   

12.
Advances in the quantification of rare earth elements (REE) at the micrometric scale in uranium oxides by laser ablation‐inductively coupled plasma‐mass spectrometry are described. The determination of the best analytical conditions was tested using a uranium oxide (Mistamisk) the concentrations of REE in which were previously estimated by other techniques. Comparison between the use of U or Pb as an internal standard clearly showed a diameter‐dependent fractionation effect related to Pb at small crater diameters (16 and 24 μm), which was not found for U. The quantification of REE contents in uranium oxide samples using both matrix‐matched (uranium oxide) and non‐matrix‐matched (NIST SRM 610 certified glass) external calibrators displayed no significant difference, demonstrating a limited matrix effect for REE determination by LA‐ICP‐MS. Moreover, no major interferences on REEs were detected. The proposed methodology (NIST SRM 610 as external calibrator and U as internal standard) was applied to samples from uranium deposits from around the world. The results showed that LA‐ICP‐MS is a suitable analytical technique to determine REE down to the μg g?1 level in uranium oxides at the micrometre scale and that this technique can provide significant insights into uranium metallogeny.  相似文献   

13.
Here we report uranium and thorium isotopic ratios and elemental concentrations measured in solid reference materials from the USGS (BHVO‐2G, BCR‐2G, NKT‐1G), as well as those from the MPI‐DING series (T1‐G, ATHO‐G). Specifically created for microanalysis, these naturally‐sourced glasses were fused from rock powders. They cover a range of compositions, elemental concentrations and expected isotopic ratios. The U‐Th isotopic ratios of two powdered source materials (BCR‐2, BHVO‐2) were also characterised. These new measurements via multi‐collector thermal ionisation mass spectrometry and multi‐collector inductively coupled plasma‐mass spectrometry can now be used to assess the relative performance of techniques and facilitate comparison of U‐Th data amongst laboratories in the geoscience community for in situ and bulk analyses.  相似文献   

14.
相山矿田热液水云母化及其与铀矿化关系研究   总被引：7，自引：2，他引：5  
相山铀矿田广泛发育热液水云母化,且水云母以伊利石、蒙皂石混层矿物居多。对典型矿床围岩、蚀变岩石和矿石中粘土组成的定量分析和化学成分分析表明：随着Ｕ元素的逐渐富集,粘土矿物存在蒙皂石→伊利石、蒙皂石混层矿物→伊利石的转化过程,而且这一转化过程在本区是一个动态的平衡过程,这一研究结果很好解释了相山矿田以群脉矿床的为主的特征;蚀变岩石中高蒙皂石含量的粘土矿物为后期富大矿起了富集Ｕ的作用。  相似文献   

15.
This study provides a measurement of success rate of Raman spectroscopy for mineral identification, and a direct comparison of powder X‐ray diffraction (PXRD) is provided by applying the same procedure for measuring its success rate against the identical set of samples. Consistent, standardised analytical procedures were applied to a set of fifty‐five minerals, and a success score was assigned to the results of each analytical method for each sample. For each analytical method, an average success rate (on a scale of 0–100) was calculated from these success scores. The success rate measured for powder XRD is 89, while the success rate for Raman spectroscopy came to 77. As the most common analytical challenge in Raman spectroscopy is specimen photoluminescence (PL), an estimate of the impact of technological advances that would eliminate this interference is provided by recalculating the success rate after removing the samples that produced PL interference from consideration. The resulting no‐PL success rate of 90 indicates that the success rate of Raman spectroscopy would be quite comparable to powder XRD if PL interference could be removed from Raman spectra.  相似文献   

16.
These mature analytical techniques do not show any change in publication level from the previous two years and AAS remains dominant in terms of the number of publications. The last two years have seen fewer technical improvements than in the previous review period. Some interesting papers dealing with uncertainty and quality assurance in INAA were published during 2006–2007. It is suggested that photon activation should be reconsidered because the source of electron accelerators has recently improved. A technique to preconcentrate Se for INAA determination has also been proposed. In the case of AAS, papers on analyte preconcentration continue to be more abundant than those relating to instrumental modification. Sample preparation for AAS is also active and ultrasound‐assisted leaching shows some promising applications. There were an unusual number of reviews concerned with AAS and those important to geological samples are cited here. A technique to preconcentrate Cr in water is presented and a new device to determine As and Se is showing some potential uses. Confocal X‐ray mapping continues to show interesting developments. One group developed a technique to perform XRF inside an oyster and an interesting application of μ‐XRF mapping of sediments is presented. Determination of platinum‐group elements (at μg g1 concentrations) can be carried out very quickly with an improved XRF technique.  相似文献   

17.
Depending upon oxygen fugacity, uranium exists in three different oxidation states in magmatic silicate liquids. The hexavalent state, present as the uranyl group, UO2+2, is stable under highly oxidizing conditions, but can still be detected in the presence of the NiNiO buffer. Under the same conditions the pentavalent state forms about 30–40% of total uranium and is also characteristic of relatively high oxygen fugacities. Optical absorption spectra obtained on granitic and basaltic glasses synthesized in the presence of the NiNiO buffer are very different: this is interpreted as being due to the presence of UO+2 complexes in the former and 6-coordinated U(V) in the latter. The tetravalent state is the most stable under reducing conditions: at the FeFeO buffer, it is the only one present. An 8-coordinated U(IV) species seems the most probable, by comparison of the spectra with those of crystallized U(IV) compounds. The trivalent state was not detected, even under the most reducing conditions. Interpretation of the spectra obtained in the glasses in terms of coordination and bonding is however difficult, due to the lack of knowledge of 5f-systems in iono-covalent systems such as oxide glasses. The presence of the pentavalent state must be taken into account in discussing partition coefficients of uranium and trans-uranium compounds in natural and synthetic systems (because of the effect of oxygen fugacity and oxide ion activity on the U(IV) U(V) system). During postmagmatic hydrothermal processes U(V) is destroyed, resulting in the early precipitation of U(IV) containing minerals and possible migration of uranyl ions.  相似文献   

18.
新疆伊犁盆地砂岩型铀矿床,由于规模大、成矿环境和成矿条件好,在同类型矿床中具有良好的代表性,研究矿床的成矿作用对今后找矿勘查以及开采具有重要理论意义。本文在区域赋铀层位沉积环境研究基础上,以赋矿围岩为研究主体,对伊犁盆地典型铀矿床沉积序列和矿床的控矿层位开展研究,通过对赋矿沉积层位中粘土质对铀矿成矿的控制作用及与铀矿的空间联系和成因分析,开展系统的铀矿床学、能谱测试、显微结构、扫描电镜、地球化学、氢氧同位素等研究,特别是开展了富矿砂体中粘土矿物的种类、成分、结构、同位素、成因等的研究,对粘土质矿物对铀矿成矿的控制作用进行了系统研究。通过研究粘土矿物在伊犁盆地蒙其古尔砂岩型铀矿床成矿过程中的作用及与铀矿的空间联系和成因分析表明:粘土矿物在层间氧化带中分布较为广泛,在主要矿体的氧化还原过渡带中,尤其是部分具有强烈粘土蚀变的砂岩层中铀含量较其他层位要高,反映出粘土矿物与铀成矿是有成因关联的。通过系统的扫描电镜、能谱测试研究,从微观证明粘土矿物与铀成矿有相关关系;粘土矿物的存在导致在近地表含氧含铀水在经过砂岩孔隙时被具有较强吸附能力和巨大表面自由能的粘土矿物所吸附,形成了铀含量较高的片状,团块状的粘土矿物,其在铀成矿作用中起到了吸附和界面的作用,有利于赋矿空间的形成及定位。结合沉积作用、构造活动和后期流体成矿作用等因素,分析了成矿机制和成矿作用,赋矿层位中的粘土矿物、其它成矿条件如岩性(赋矿层和矿源层)、构造(对铀矿化的动力和对地下水径流及铀矿体)等共同控制了铀成矿作用。  相似文献   

19.
Quantitative X‐ray diffraction analysis of the <2 mm sediment fraction was carried out on 1257 samples (from the seafloor and 16 cores) from the Iceland shelf west of 18° W. All but one core (B997‐347PC) were from transects along troughs on the NW to N‐central shelf, an area that in modern and historic times has been affected by drift ice. The paper focuses on the non‐clay mineralogy of the sediments (excluding calcite and volcanic glass). Quartz and potassium feldspars occupy similar positions in an R‐mode principal component analysis, and oligoclase feldspar tracks quartz; these minerals are used as a proxy for ice‐rafted detritus (IRD). Accordingly, the sum of these largely foreign minerals (Q&K) (to Icelandic bedrock) is used as a proxy for drift ice. A stacked, equi‐spaced 100 a record is developed which shows both low‐frequency trends and higher‐frequency events. The detrended stacked record compares well with the flux of quartz (mg cm?2 a?1) at MD99‐2269 off N Iceland. The multi‐taper method indicated that there are three significant frequencies at the 95% confidence level with periods of ca. 2500, 445 and 304 a. Regime shift analysis pinpoints intervals when there was a statistically significant shift in the average Q&K weight %, and identifies four IRD‐rich events separated by intervals with lower inputs. There is some association between peaks of IRD input, less dense surface waters (from δ18O data on planktonic foraminifera) and intervals of moraine building. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

20.
Micro‐X‐ray fluorescence scanning spectroscopy of marine and lake sedimentary sequences can provide detailed palaeoenvironmental records through element intensity proxy data. However, problems with the effects of interstitial pore water on the micro‐X‐ray fluorescence intensities have been pointed out. This is because the X‐ray fluorescence intensities are measured directly at the surfaces of split wet sediment core samples. This study developed a new method for correcting X‐ray fluorescence data to compensate for the effects of pore water using a scanning X‐ray analytical microscope. This involved simultaneous use of micro‐X‐ray fluorescence scanning spectroscopy and an X‐ray transmission detector. To evaluate the interstitial pore water content from the X‐ray transmission intensities, a fine‐grained sediment core retrieved from Lake Baikal (VER99‐G12) was used to prepare resin‐embedded samples with smooth surfaces and uniform thickness. Simple linear regression between the linear absorption coefficients of the samples and their porosity, based on the Lambert–Beer law, enabled calculation of the interstitial pore spaces and their resin content with high reproducibility. The X‐ray fluorescence intensities of resin‐embedded samples were reduced compared with those of dry sediment samples because of: (i) the X‐ray fluorescence absorption of resin within sediment; and (ii) the sediment dilution effects by resin. An improved micro‐X‐ray fluorescence correction equation based on X‐ray fluorescence emission theory considers the instrument's sensitivity to each element, which provides a reasonable explanation of these two effects. The resin‐corrected X‐ray fluorescence intensity was then successfully converted to elemental concentrations using simple linear regression between the data from micro‐X‐ray fluorescence scanning spectroscopy and from the conventional analyzer. In particular, the calculated concentration of SiO2 over the depth of the core, reflecting diatom/biogenic silica concentration, was significantly changed by the calibrations, from a progressively decreasing trend to an increasing trend towards the top of the core.  相似文献   

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