Geochemistry地球化学

Geochemistry(英文缩写 GEOCHEMISTRY-GERMANY),ISSN 0009-2819,eISSN 1611-5864,中文译名:地球化学 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
3.000
JCR 分区
Q2
CAS 分区
B3
近一年发文量
0
本站 PubMed 收录统计

发文量统计区间:2025-09-27 至 2026-09-27,按本站收录文献的发表日期统计。

ISSN: 0009-2819 · eISSN: 1611-5864 · 缩写: GEOCHEMISTRY-GERMANY ·中文: 地球化学

期刊介绍

选择期刊介绍栏目

期刊简介

Geochemistry 是一本聚焦地球化学及其相关交叉领域的国际期刊,涵盖岩石学、矿床学、环境地球化学和宇宙化学等方向。该刊注重元素与同位素地球化学方法在解决地质过程、资源勘查和环境问题中的应用,读者群包括地球科学研究者、地质调查人员及环境科学工作者。

研究方向

主要发表岩石地球化学、矿床地球化学、同位素地球化学、有机地球化学、环境地球化学及宇宙化学等方向的研究论文、综述和短讯,强调地球化学方法在理解地质过程、资源形成机制和环境演化中的应用。

期刊特色

该刊偏好基于实测数据与地球化学分析的研究,论文通常具有明确的地质背景和区域意义,方法学上重视同位素和微量元素示踪。适合从事基础地质、矿产勘查和环境地球化学研究的科研人员与研究生阅读和投稿。

投稿难度

投稿难度中等偏上,对数据质量和地质解释的严谨性要求较高。建议在投稿前充分梳理区域地质背景,确保分析测试方法描述完整、数据支撑充分,并针对审稿人可能关注的地球化学过程机制进行深入讨论。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20214.127Q2
20223.700Q2
20232.600Q2
20242.900Q2
20253.000Q2

Geochemistry 最新收录文献

  1. JCR分区: Q2 CAS分区: B3 影响因子: 3

    1. Geochemistry and Cosmochemistry of Potassium Stable Isotopes.

    作者:
    Kun Wang, Weiqiang Li, Shilei Li, Zhen Tian, Piers Koefoed, Xin-Yuan Zheng
    日期:
    2021-09-01

    Stable potassium isotopes are one of the emerging non-traditional isotope systems enabled in recent years by the advance of Multi-Collector Inductively-Coupled-Plasma Mass-Spectrometry (MC-ICP-MS). In this review, we first summarize the geochemical and cosmochemical properties of K, its major reservoirs, and the analytical methods of K isotopes. Following this, we review recent literature on K isotope applications in the fields of geochemistry and cosmochemistry. Geochemically, K is a highly incompatible lithophile element, and a highly soluble, biophile element. The isotopic fractionation of K is relatively small during magmatic processes such as partial melting and fractional crystallization, whereas during low-temperature and biological processes fractionation is considerably larger. This resolvable fractionation has made K isotopes promising tracers for a variety of Earth and environmental processes, including chemical weathering, low-temperature alteration of igneous rocks, reverse weathering, and the recycling of sediments into the mantle during subduction. Sorption and interactions of aqueous K with different clay minerals during cation exchange and clay formation are likely to be of fundamental significance in generating much of the K isotope variability seen in samples from the Earth surface and samples carrying recycled surface materials from the deep Earth. The magnitude of this fractionation is process- and mineral-dependent. Comprehensive quantification of pertinent K isotope fractionation factors is currently lacking and urgently needed. Significant fractionation during biological activities, such as plant uptake, demonstrates the potential utility of K isotopes in the study of the nutrient cycle and its relation to the climate and various ecosystems, enabling new and largely unexplored avenues for future research. Of significant importance to the cosmochemistry community, K is a moderately volatile element with large variations in K/U ratio observed among chondrites and planetary materials. As this indicates different degrees of volatile depletion, it has become a fundamental chemical signature of both chondritic and planetary bodies. This volatile depletion has been attributed to various processes such as solar nebula condensation, mixing of volatile-rich and -poor reservoirs, planetary accretional volatilization via impacts, and/or magma ocean degassing. While K isotopes have the potential to distinguish these different processes, the current results are still highly debated. A good correlation between the K isotope compositions of four differentiated bodies (Earth, Mars, Moon, and Vesta) and their masses suggests a ubiquitous volatile depletion mechanism during the formation of the terrestrial planets. It is still unknown whether any of the K isotopic variation among chondrites and differentiated bodies can be attributed to inherited signatures of mass-independent isotopic anomalies.

  2. JCR分区: Q2 CAS分区: B3 影响因子: 3

    2. Habitability of Hydrothermal Systems at Jezero and Gusev Craters as Constrained by Hydrothermal Alteration of a Terrestrial Mafic Dike.

    作者:
    Lacey J Costello, Justin Filiberto, Jake R Crandall, Sally L Potter-McIntyre, Susanne P Schwenzer, Michael A Miller, Daniel R Hummer, Karen Olsson-Francis, Scott Perl
    日期:
    2020-05-01

    NASA's search for habitable environments has focused on alteration mineralogy of the Martian crust and the formation of hydrous minerals, because they reveal information about the fluid and environmental conditions from which they precipitated. Extensive work has focused on the formation of alteration minerals at low temperatures, with limited work investigating metamorphic or high-temperature alteration. We have investigated such a site as an analog for Mars: a mafic dike on the Colorado Plateau that was hydrothermally altered from contact with groundwater as it was emplaced in the porous and permeable Jurassic Entrada sandstone. Our results show evidence for fluid mobility removing Si and K but adding S, Fe, Ca, and possibly Mg to the system as alteration progresses. Mineralogically, all samples contain calcite, hematite, and kaolinite; with most samples containing minor anatase, barite, halite, and dolomite. The number of alteration minerals increase with alteration. The hydrothermal system that formed during interaction of the magma (heat source) and groundwater would have been a habitable environment once the system cooled below ~120° C. The mineral assemblage is similar to alteration minerals seen within the Martian crust from orbit, including those at Gusev and Jezero Craters. Therefore, based on our findings, and extrapolating them to the Martian crust, these sites may represent habitable environments which would call for further exploration and sample return of such hydrothermally altered igneous materials.

  3. JCR分区: Q2 CAS分区: B3 影响因子: 3

    3. {"_":"Origin of O-rich fine-grained Ca-Al-rich inclusions of different mineralogy and texture.","sup":["16"]}

    作者:
    Jangmi Han, Benjamin Jacobsen, Ming-Chang Liu, Adrian J Brearley, Jennifer E Matzel, Lindsay P Keller
    日期:
    2019-12-01

    A coordinated mineralogical and oxygen isotopic study of four fine-grained calcium-, aluminum-rich inclusions (CAIs) from the ALHA77307 CO3.0 carbonaceous chondrite was conducted. Three of the inclusions studied, 05, 1-65, and 2-119, all have nodular structures that represent three major groups, melilite-rich, spinel-rich, and hibonite-rich, based on their primary core mineral assemblages. A condensation origin was inferred for these CAIs. However, the difference in their primary core mineralogy reflects unique nebular environments in which multiple gas-solid reactions occurred under disequilibrium conditions to form hibonite, spinel, and melilite with minor perovskite and Al,Ti-rich diopside. A common occurrence of a diopside rim on the CAIs records a widespread event that marks the end of their condensation as a result of isolation from a nebular gas. An exception is a rare inclusion 2-112 that contains euhedral spinel crystals embedded in melilite, suggesting this CAI had been re-melted. All of the fine-grained CAIs analyzed in ALHA77307 are uniformly O-rich with an average ΔO value of ~-22 ± 5‰ (2σ), indicating no apparent correlation between their textures and oxygen isotopic compositions. We therefore conclude that a prevalent O-rich gas reservoir existed in a region of the solar nebula where CO3 fine-grained CAIs formed, initially by condensation and then later, some of them were reprocessed by melting event(s).

  4. JCR分区: Q2 CAS分区: B3 影响因子: 3

    4. The nature, origin and modification of insoluble organic matter in chondrites, the possibly interstellar source of Earth's C and N.

    作者:
    C M O'D Alexander, G D Cody, B T De Gregorio, L R Nittler, R M Stroud
    日期:
    2017-05-01

    All chondrites accreted ~3.5 wt.% C in their matrices, the bulk of which was in a macromolecular solvent and acid insoluble organic material (IOM). Similar material to IOM is found in interplanetary dust particles (IDPs) and comets. The IOM accounts for almost all of the C and N in chondrites, and a significant fraction of the H. Chondrites and, to a lesser extent, comets were probably the major sources of volatiles for the Earth and the other terrestrial planets. Hence, IOM was both the major source of Earth's volatiles and a potential source of complex prebiotic molecules. Large enrichments in D and N, relative to the bulk solar isotopic compositions, suggest that IOM or its precursors formed in very cold, radiation-rich environments. Whether these environments were in the interstellar medium (ISM) or the outer Solar System is unresolved. Nevertheless, the elemental and isotopic compositions and functional group chemistry of IOM provide important clues to the origin(s) of organic matter in protoplanetary disks. IOM is modified relatively easily by thermal and aqueous processes, so that it can also be used to constrain the conditions in the solar nebula prior to chondrite accretion and the conditions in the chondrite parent bodies after accretion. Here we review what is known about the abundances, compositions and physical nature of IOM in the most primitive chondrites. We also discuss how the IOM has been modified by thermal metamorphism and aqueous alteration in the chondrite parent bodies, and how these changes may be used both as petrologic indicators of the intensity of parent body processing and as tools for classification. Finally, we critically assess the various proposed mechanisms for the formation of IOM in the ISM or Solar System.

  5. JCR分区: Q2 CAS分区: B3 影响因子: 3

    5. Major and trace element geochemistry of Lake Bogoria and Lake Nakuru, Kenya, during extreme draught.

    作者:
    Franz Jirsa, Martin Gruber, Anja Stojanovic, Steve Odour Omondi, Dieter Mader, Wilfried Körner, Michael Schagerl
    日期:
    2013-10-01

    The physico-chemical properties of water samples from the two athalassic endorheic lakes Bogoria and Nakuru in Kenya were analysed. Surface water samples were taken between July 2008 and October 2009 in weekly intervals from each lake. The following parameters were determined: pH, salinity, electric conductivity, dissolved organic carbon (DOC), the major cations (FAAS and ICP-OES) and the major anions (IC), as well as certain trace elements (ICP-OES). Samples of superficial sediments were taken in October 2009 and examined using Instrumental Neutron Activation Analysis (INAA) for their major and trace element content including rare earth elements (REE). Both lakes are highly alkaline with a dominance of Na > K > Si > Ca in cations and HCO > CO > Cl > F > SO in anions. Both lakes also exhibited high concentrations of Mo, As and fluoride. Due to an extreme draught from March to October 2009, the water level of Lake Nakuru dropped significantly. This created drastic evapoconcentration, with the total salinity rising from about 20‰ up to 63‰. Most parameters (DOC, Na, K, Ca, F, Mo and As) increased with falling water levels. A clear change in the quality of DOC was observed, followed by an almost complete depletion of dissolved Fe from the water phase. In Lake Bogoria the evapoconcentration effects were less pronounced (total salinity changed from about 40‰ to 48‰). The distributions of REE in the superficial sediments of Lake Nakuru and Lake Bogoria are presented here for the first time. The results show a high abundance of the REE and a very distinct Eu depletion of Eu/Eu* = 0.33-0.45.

  6. JCR分区: Q2 CAS分区: B3 影响因子: 3

    6. Origin of tektites: an alternative to terrestrial impact theory.

    作者:
    E P Izokh
    日期:
    1996-01-01

    The Terrestrial Impact Theory (TIT) has won a complete victory over O'Keefe's lunar volcanic theory, but only because the Moon appears to be the wrong place for tektites. Indeed, the TIT ignores strong evidence of their volcanic origin--far from the Moon. The Extraterrestrial Volcanic Comet Theory proposes an alternative to both of these theories. Major arguments for an extraterrestrial tektite source are paradoxical: a great time difference between tektite formation and their arrival on Earth, and also forms, plastic deformations, ice collision marks, vacuum voids, etc. indicating specific conditions of tektite formation such as low gravitational field, lack of atmosphere, interaction of hot plastic tektites with ice, etc. Major evidence of volcanic origin includes: close analogy between shaped tektites and small volcanic bombs, and between layered tektites and lava or tuff-lava flows or huge bombs; analogy between flanged tektites and volcanic bombs ablated by gasjets: long-time, multistage formation of some tektites that corresponds to wide variations in their radiometric ages; well-ordered long compositional trends (series) typical of magmatic differentiation; different compositional tektite families (subseries) comparable to different stages (phases) of the volcanic process. Thus, different types of volcanic eruptions under extraterrestrial conditions could be reconstructed based on tektite properties. It is presumed that tektites were transported to the Earth by specific eruptive comets, i.e. in the form of ice-tektite agglomerates launched into space by volcanic explosion. Major arguments favouring comets include: ice collision marks and imprints as mentioned above; linear band-like sculpture of the Australasian strewn field as evidence of comet fragmentation and slope or skipping trajectory of separate fragments; compact coincidence of the Zhamanshin impact crater with small tektite strewn field as evidence of steep trajectory of separate comet fragments that disintegrated while entering the atmosphere. The comet-Earth collision under consideration happened 10,000 years ago and caused the global catastrophe marked by the sharp Pleistocene-Holocene boundary, i.e. by abrupt climatic changes, the end of glaciation, mass extinction, etc. This event can be compared with the "dinosaur" catastrophe at the K/T boundary 65 Ma, which was also accompanied by tektite fall.

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指标接近的期刊