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1.
Detailed chemostratigraphy across the Cenomanian-Turonian boundary in northern Tunisia points to several prevailing paleoceanographic conditions during the deposition of organic-rich beds of Bahloul Formation. The sedimentological study shows that there is no correlation between color and CaCO3 content because both dark and light-colored intervals of Bahloul Formation are carbonate-rich. Stable isotope analysis displays a positive carbon isotope excursion characterized by four significant peaks (I to IV) which are ranging from 3.2 to 3.5‰. These peaks represent episodes of elevated rates of organic carbon burial during the C/T oceanic anoxic event (C/T boundary OAE2). The Cenomanian-Turonian boundary could be situated between the third isotopic peak and the filament event. The total organic carbon (TOC) measurements show values ranging from 0.28 to 6.19% with average value of 3.5%. This indicates that the Bahloul Formation shale is a very good oil source rock. The Hydrogen Index (HI) values range from 359 to 698 mg HC/g TOC. The T max values range from 390 to 438 °C. Binary diagrams HI vs. T max indicate a type II with values falling within the immature organic-matter range. The concentrations major elements reveal low values of Ti and K. The correlation between Al and Ti and K shows a significant correlation pointing to homogeneous provenance. Primary productivity indicators (Cu, Ba, and Ni) record its association with organic matter. Redox-sensitive elements such as U, V, and Mo and the high values of V/(V + Ni) ratio indicate a strongly reducing environment which led to the better preservation of the organic matter.  相似文献   

2.
The iron mineralization is hosted in carbonate beds of the Garagu Formation (Early Cretaceous) at Gara Mountain, Duhok Governorate, Kurdistan Region, NE Iraq. The Garagu Formation is composed of a series of limestone and siltstone beds with iron-rich beds in the middle part. The iron-rich limestones are iron-rich oolitic grainstone and bioclastic wackestone with hematite and goethite minerals. Geochemical results drawn from this study indicate that the percentage of iron in these beds reaches 19.73 %. Moreover, petrographical investigation of thin and polished sections reveals the presence of different types of fossils, indicating an open marine interior platform depositional environment. Different iron minerals, including hematite, goethite, siderite, pyrite and magnetite, were identified in the sections, and their geneses were related to syngenetic and diagenetic processes. The geochemical distribution of major and trace elements, as well as the V/Ni, V/(V+Ni), V/Cr and Sr/Ba ratios, indicates a reducing environment during the precipitation of carbonate sediments and a subsequent oxidizing condition during the concentration of iron minerals via diagenesis.  相似文献   

3.
Magnetite and hematite are common minerals in a range of mineral deposit types. These minerals form partial to complete solid solutions with magnetite, chromite, and spinel series, and ulvospinel as a result of divalent, trivalent, and tetravalent cation substitutions. Electron microprobe analyses of minor and trace elements in magnetite and hematite from a range of mineral deposit types (iron oxide-copper-gold (IOCG), Kiruna apatite–magnetite, banded iron formation (BIF), porphyry Cu, Fe-Cu skarn, Fe-Ti, V, Cr, Ni-Cu-PGE, Cu-Zn-Pb volcanogenic massive sulfide (VMS) and Archean Au-Cu porphyry and Opemiska Cu veins) show compositional differences that can be related to deposit types, and are used to construct discriminant diagrams that separate different styles of mineralization. The Ni + Cr vs. Si + Mg diagram can be used to isolate Ni-Cu-PGE, and Cr deposits from other deposit types. Similarly, the Al/(Zn + Ca) vs. Cu/(Si + Ca) diagram can be used to separate Cu-Zn-Pb VMS deposits from other deposit types. Samples plotting outside the Ni-Cu-PGE and Cu-Zn-Pb VMS fields are discriminated using the Ni/(Cr + Mn) vs. Ti + V or Ca + Al + Mn vs. Ti + V diagrams that discriminate for IOCG, Kiruna, porphyry Cu, BIF, skarn, Fe-Ti, and V deposits.  相似文献   

4.
邱振  王清晨 《地质科学》2012,(4):1085-1098
通过对来宾地区蓬莱滩剖面和铁桥剖面中二叠统(茅口组)与上二叠统(合山组)TOC、古生产力(Ba/Al)以及保存条件(V/Cr、V/(V+Ni)等)等指标的研究,认为本区仅蓬莱滩剖面局部发育优质烃源岩(TOC平均可达3％),缺氧的盆地环境是本区烃源岩发育的主控因素。结合区域研究资料,认为黔桂盆地整体上不发育上二叠统烃源岩,可能与这一时期以峨眉山地幔柱为代表的区域性地壳隆升作用有关。  相似文献   

5.
The Blue Dot gold deposit, located in the Archean Amalia greenstone belt of South Africa, is hosted in an oxide (± carbonate) facies banded iron formation (BIF). It consists of three stratabound orebodies; Goudplaats, Abelskop, and Bothmasrust. The orebodies are flanked by quartz‐chlorite‐ferroan dolomite‐albite schist in the hanging wall and mafic (volcanic) schists in the footwall. Alteration minerals associated with the main hydrothermal stage in the BIF are dominated by quartz, ankerite‐dolomite series, siderite, chlorite, muscovite, sericite, hematite, pyrite, and minor amounts of chalcopyrite and arsenopyrite. This study investigates the characteristics of gold mineralization in the Amalia BIF based on ore textures, mineral‐chemical data and sulfur isotope analysis. Gold mineralization of the Blue Dot deposit is associated with quartz‐carbonate veins that crosscut the BIF layering. In contrast to previous works, petrographic evidence suggests that the gold mineralization is not solely attributed to replacement reactions between ore fluid and the magnetite or hematite in the host BIF because coarse hydrothermal pyrite grains do not show mutual replacement textures of the oxide minerals. Rather, the parallel‐bedded and generally chert‐hosted pyrites are in sharp contact with re‐crystallized euhedral to subhedral magnetite ± hematite grains, and the nature of their coexistence suggests that pyrite (and gold) precipitation was contemporaneous with magnetite–hematite re‐crystallization. The Fe/(Fe+Mg) ratio of the dolomite–ankerite series and chlorite decreased from veins through mineralized BIF and non‐mineralized BIF, in contrast to most Archean BIF‐hosted gold deposits. This is interpreted to be due to the effect of a high sulfur activity and increase in fO2 in a H2S‐dominant fluid during progressive fluid‐rock interaction. High sulfur activity of the hydrothermal fluid fixed pyrite in the BIF by consuming Fe2+ released into the chert layers and leaving the co‐precipitating carbonates and chlorites with less available ferrous iron content. Alternatively, the occurrence of hematite in the alteration assemblage of the host BIF caused a structural limitation in the assignment of Fe3+ in chlorite which favored the incorporation of magnesium (rather than ferric iron) in chlorite under increasing fO2 conditions, and is consistent with deposits hosted in hematite‐bearing rocks. The combined effects of reduction in sulfur contents due to sulfide precipitation and increasing fO2 during progressive fluid‐rock interactions are likely to be the principal factors to have caused gold deposition. Arsenopyrite–pyrite geothermometry indicated a temperature range of 300–350°C for the associated gold mineralization. The estimated δ34SΣS (= +1.8 to +2.5‰) and low base metal contents of the sulfide ore mineralogy are consistent with sulfides that have been sourced from magma or derived by the dissolution of magmatic sulfides from volcanic rocks during fluid migration.  相似文献   

6.
A new occurrence of Mn-rich rocks was discovered within the high-pressure/low-temperature metamorphic rocks on the Palos peninsula of Syros (Greece). Near the summit of Mount Príonas, a meta-conglomerate consists of calcite (~63 wt%), pink manganian phengite, blue–purple manganian aegirine–jadeite, microcline, albite and quartz. In addition, it contains abundant braunite-rich aggregates (up to ~1.5 cm in diameter) that include hollandite [(Ba0.98–1.02K<0.01Na<0.02Ca<0.03) (Mn 1.02–1.52 3+ Fe 0.38–0.88 3+ Ti0.29–0.92Mn 5.11–5.76 4+ )O16], barite and manganian hematite. Due to metamorphic recrystallization and deformation, the contacts between clasts and matrix are blurred and most clasts have lost their identity. In back-scattered electron images, many aegirine–jadeite grains appear patchy and show variable jadeite contents (Jd10–67). These pyroxenes occur in contact with either quartz or albite. Manganian phengite (3.41–3.49 Si per 11 oxygen anions) is of the 3T type and contains 1.4–2.2 wt% of Mn2O3. At the known P–T conditions of high-pressure metamorphism on Syros (~1.4 GPa/ 470 °C), the mineral sub-assemblage braunite + quartz + calcite (former aragonite) suggests high oxygen fugacities relative to the HM buffer (+7 ≤ ?fO2 ≤ + 17) and relatively high CO2 fugacities. The exact origin of the conglomerate is not known, but it is assumed that the Fe–Mn-rich and the calcite-rich particles originated from different sources. Braunite has rather low contents of Cu (~0.19 wt%) and the concentrations of Co, Ni and Zn are less than 0.09 wt%. Hollandite shows even lower concentrations of these elements. Furthermore, the bulk-rock compositions of two samples are characterized by low contents of Cu, Co and Ni, suggesting a hydrothermal origin of the manganese ore. Most likely, these Fe–Mn–Si oxyhydroxide deposits consisted of ferrihydrite, todorokite, birnessite, amorphous silica (opal-A) and nontronite. Al/(Al + Fe + Mn) ratios of 0.355 and 0.600 suggest the presence of an aluminosilicate detrital component.  相似文献   

7.
The 2,058 ± 4 Ma mafic–ultramafic Kevitsa intrusion is located in the Central Lapland greenstone belt, northern Finland. It is hosted by a Paleoproterozoic volcano–sedimentary sequence that contains komatiitic volcanic rocks and sulfide- and graphite-rich black schists. Economic Ni–Cu–(PGE) sulfide mineralization occurs in the middle part of the ultramafic lower unit of the intrusion. Two main types of ore are distinguished, “normal” and “Ni–PGE” ores. The normal ore is characterized by ~2 to 6 vol% disseminated sulfides and average Ni and Cu grades of 0.3 and 0.42 wt %, respectively (Ni/Cu < 1). The Ni–PGE ore has broadly similar sulfide contents, but a higher Ni grade and lower Cu grade. As a result, the Ni/Cu ratio reaches 15, much higher than in the normal ore. The Ni–PGE ores occur as irregular, discontinuous, lense-like bodies in the ultramafic rocks. Notably, the olivines in the Ni–PGE ore contain extremely high Ni contents of up to 14,000 ppm, which is significantly higher than the Ni content of olivine in other mafic–ultramafic igneous rocks globally (up to ~5,000 ppm) and in harmony with the associated Ni-rich sulfide assemblage containing pentlandite, millerite and pyrite. Microprobe mapping of olivine from the Ni–PGE ore suggests relatively low and homogeneous S contents and homogeneous distribution of Ni, Mg, Fe, which is inconsistent with the presence of sulfide inclusions in the olivine grains, or diffusion of Ni from interstitial sulfides into the olivine grains. We therefore conclude that Ni substitutes for Mg in the olivine lattice. The clinopyroxenes from the Ni–PGE ore also have unusually high Ni concentrations reaching 1,500 ppm and show a positive correlation with the nickel content of the associated olivine. The Nicpx/Niolivine is ~0.1 to 0.2 corresponding to high T partitioning of Ni between clinopyroxene and olivine. K D of 20 can account for the partitioning of nickel between olivine and the sulfide phase, consistent with magmatic equilibration. These data suggest that the olivine, clinopyroxene, and sulfides all crystallized from a basaltic magma with an unexceptionally high Ni content ranging from 300 to 1,100 ppm. The Ni–PGE ores are spatially associated with ultramafic xenoliths. Olivine in these ultramafic xenoliths have relatively high Fo contents (up to 90 mol %) and high Ni contents (up to 5,200 ppm) suggesting that the xenoliths formed from a komatiitic parental magma. It is proposed that assimilation by the Kevitsa magma of massive or semi-massive sulfides associated with komatiitic rocks elevated the Ni content of the magma and resulted in the formation of Ni–PGE ores and related extremely Ni-rich olivines.  相似文献   

8.
Vein-stockwork magnesite in the Madenli area, sedimentary huntite-magnesite in the A?a??t?rtar area, and lacustrine hydromagnesite in the Salda Lake area are located in the Bey?ehir-Hoyran and Lycian nappe rocks around Isparta and Burdur, Southwest Anatolia. The aim of this study is to understand trace element contents and carbon-oxygen isotope ratios in different originated magnesite, magnesite bearing huntite, and hydromagnesite deposits. Also, the element contents and isotope ratios of the magnesite occurrences are to compare with each other and similar magnesite occurrences in Turkey and world. It is found that the Madenli magnesite occurrences in the ?arkikaraa?aç ophiolites, A?a??t?rtar magnesite bearing huntite deposits in the lacustrine rocks of the Miocene-Pliocene, and the Salda hydromagnesite deposits in lacustrine basin on the Ye?ilova ophiolites. The paragenesis contains a common carbonate mineral magnesite, less calcite, serpentine, smectite, dolomite, and talc in the Madenli magnesite occurrences, mostly huntite and locally magnesite, dolomite, calcite, illite, quartz, and smectite in the A?a??t?rtar huntite-magnesite occurrences, and only hydromagnesite mineral in the Salda Lake hydromagnesite occurrences. Vein and stockwork Madenli magnesite deposits were recognized by higher total iron oxide concentrations (mean 1.10 wt%) than sedimentary A?a??t?rtar magnesite bearing huntite (mean 0.13 wt%) and lacustrine Salda hydromagnesite (mean 0.22 wt%) deposits. It is suggested that high Fe content (up to 5%) in the magnesite associated with ultramafic rocks than those from sedimentary environments (≤1% Fe). Based on average Ni, Co, Ba, Sr, As and Zr contents in the magnesite deposits, average Ni (134.63 ppm) and Co (15.19 ppm) contents in the Madenli magnesite and Salda hydromagnesite (36.85 ppm for Ni, 3.15 ppm for Co) have higher values than A?a??t?rtar huntite + magnesite (7.67 ppm for Ni and 0.89 ppm for Co). Average Ni-Co contents of these deposits can have close values depending on ophiolite host rock. Average Ba values of the Madenli (108.09 ppm) and A?a??t?rtar (115.88 ppm) areas are higher than those of Salda hydromagnesite (13.15 ppm). Sediment-hosted A?a??t?rtar magnesite-huntite deposits have the highest Sr contents (mean 505.81 ppm) as reasonably different from ultrabasic rock-related Madenli magnesite (mean 38.76 ppm) and Salda hydromagnesite (mean 36.70 ppm). The highest Sr content of sedimentary A?a??t?rtar deposits reveals that Sr is related to carbonate rocks. As and Zr contents have the highest average values (As 52.76 ppm and Zr 9.67 ppm) in the A?a??t?rtar deposits different from Madenli magnesite (As 0.54 ppm and Zr 1.67 ppm) and Salda hydromagnesite (As 0.5 ppm and Zr 2.58 ppm) deposits. High As and Zr concentrations in the A?a??t?rtar magnesite-huntite deposits may come from volcanic rocks in near country rocks. The δ 13C (PDB) isotope values vary between ?10.1 and ?11.4‰ in the Madenli magnesite, 7.8 to 8.8‰ for huntite, 1.7 to 8.3‰ for huntite + magnesite and 4.0‰ for limestone + magnesite in the A?a??t?rtar huntite-magnesite deposits, and 4.4 to 4.9‰ for Salda Lake hydromagnesite. The sources of the CO2 are hydrothermal solutions, meteoric waters, groundwater dissolved carbon released from fresh water carbonates and marine limestone, soil CO2, and plant C3 in the Madenli magnesite, and may be deep seated metamorphic reactions in limestone and shales of rich in terms of organic matter. The sources of CO2 in A?a??t?rtar huntite and Salda hydromagnesite were meteoric water, groundwater dissolved inorganic carbon, fresh water carbonates, and marine limestone. The δ 18O (SMOW) isotope composition ranges from 26.8 to 28.1‰ in the Madenli magnesite, 30.4 to 32.4‰ for huntite and 29.8 to 35.5‰ for huntite + magnesite and 26.9‰ for limestone + magnesite in the A?a??t?rtar area, and 36.4 to 38.2‰ in the Salda Lake hydromagnesite. The Salda Lake hydromagnesite has heavier oxygen isotopic values than others. The sources of oxygen in the Madenli magnesite deposits are hydrothermal solutions, meteoric water, freshwater carbonates, and marine limestone, but the sources of oxygen of the A?a??t?rtar magnesite-huntite are meteoric water, fresh water carbonates, and marine limestone. The Salda Lake hydromagnesite has very high δ18O isotope values indicating a strong evaporitic environment. Magnesium (Mg+2) and silica are released by disintegration of very weathered-serpentinized ultrabasic rocks of all magnesite deposits and from partly dolomite and dolomitic limestone in the A?a??t?rtar magnesite bearing huntite deposits. In the A?a??t?rtar area, calcium (Ca+2) for huntite mineralization is provided by surrounding carbonate rocks. Based on isotopic data, host rocks, petrographic properties of the Madenli magnesite can be described as an ultramafic-associated hydrothermal vein mineralization corresponding to “Kraubath type” deposits, but A?a??t?rtar ve Salda Lake deposits are sedimentary mineralization (lacustrine/evaporitic) corresponding to “Bela Stena type” deposits. The estimated temperature using average δ18O isotope values is about 33.51 °C for Madenli magnesite, 48.33 °C for A?a??t?rtar huntite-magnesite, and 25 °C for Salda hydromagnesite. Based on isotope data, we can be say that the Madenli magnesite, A?a??t?rtar magnesite-huntite, and Salda hydromagnesite occur at low to moderate-low temperature water and alkaline (pH 8.5–10.5) under surface or near-surface conditions.  相似文献   

9.
The El Espino IOCG mining district is characterized by several mineralized bodies the largest of which is the El Espino deposit, which has an estimated geologic resource of 123 Mt at 0.66 % Cu and 0.24 g/t Au. Mineralized bodies are distributed in a 7?×?10 km2 area throughout a 1,000-m vertical section. They range from single veins to stockworks and breccias to manto-type deposits. The ore bodies are hosted primarily by volcanic, volcaniclastic, and sedimentary rocks of the Early Cretaceous Arqueros and Quebrada Marquesa formations, with a few mineralized zones within Late Cretaceous dioritic intrusions. The fault and vein architecture shows that El Espino IOCG system was localized within a dilatational jog along a major transtensional dextral fault system. Sodic alteration (albite) is the most extensive style of alteration in the district, and it is bounded by major NS–NNE trending faults. Sodic–calcic (epidote–albite) alteration occurs at deep to medium elevations (1,000–500 m) and grades inward into calcic alteration. Calcic alteration surrounds dioritic intrusions of the Llahuin plutonic suite. Significant iron oxides are associated with later calcic alteration associations (actinolite–epidote–hematite). The upper portions of the alteration system (0–500 m) display hydrolytic alteration associations with abundant hematite. Hydrolytic veins are feeders to zones of manto-type alteration and mineralization within favorable volcano-sedimentary lithologies that formed El Espino deposit. Sulfides are largely confined to calcic and hydrolytic alteration associations. Hydrothermal fluids responsible for hematite and sulfide mineralization had salinities between 32 and 34 wt% NaCleq and temperature of approximately 425 °C at an estimated depth of 3–4 km. Geochronological U–Pb and 40Ar/39Ar data indicate that hydrothermal alteration was coeval with magmatic intrusive activity. One particular dioritic intrusion (88.5 Ma) preceded the calcic stage (88.4 Ma), which was accompanied by iron oxide copper and gold mineralization. Hydrolytic alteration, related to economic iron oxide copper and gold mineralization, came immediately after at 87.9 Ma.  相似文献   

10.
The black shale-hosted selenide vein-type deposit at Tilkerode, eastern Harz, Germany, has specular hematite enclosed in clausthalite (PbSe). The specular hematite has Ti and V in amounts of up to ～1 wt.% TiO2 and ～3 wt.% V2O5, and subordinate, but important, contents of Mo (22–372 ppm) and B (up to 68 ppm). The Tilkerode hematite serves as a reference for hydrothermal hematite formed at relatively low temperatures (<150 °C). The composition of the Tilkerode hematite is compared with that of two generations of specular hematite from itabirite-hosted iron-ore deposits in the Quadrilátero Ferrífero of Minas Gerais, Brazil. The first generation of specular hematite represents an early tectonic hematitisation of dolomitic itabirite at Águas Claras and occurs as fine-grained crystals. Reconnaissance data indicate that the Águas Claras hematite is poorer in Ti and V, relative to the Tilkerode hematite, but has ～5–10 ppm B and ～7–11 ppm Li. The second generation of specular hematite defines the pervasive tectonic foliation of the Gongo Soco iron ore. This hematite has Ti contents of up to ～2 wt.% TiO2 and subordinate amounts of V (62–367 ppm); its B and Li concentrations are mostly below <2 ppm B and <1 ppm Li. The presence of Ti and B in the Tilkerode hematite can be explained by highly saline, B-bearing fluids that were capable of mobilising otherwise immobile Ti. The Mo signature of the Tilkerode hematite suggests that Mo was derived from the host black shale. In Minas Gerais, B and Li were incorporated into the early tectonic hematite from saline fluids at relatively low temperatures (Águas Claras) and then released during metamorphic hematite growth at higher temperatures, as suggested by the foliation-defining hematite without B–Li signature (Gongo Soco).  相似文献   

11.
High-Mg, low-Ti volcanic rocks from the Manihiki Plateau in the Western Pacific share many geochemical characteristics with subduction-related boninites such as high-Ca boninites from the Troodos ophiolite on Cyprus, which are believed to originate by hydrous re-melting of previously depleted mantle. In this paper we compare the Manihiki rocks and Troodos boninites using a new dataset on the major and trace element composition of whole rocks and glasses from these locations, and new high-precision, electron microprobe analyses of olivine and Cr-spinel in these rocks. Our results show that both low-Ti Manihiki rocks and Troodos boninites could originate by re-melting of a previously depleted lherzolite mantle source (20–25% of total melting with 8–10% melting during the first stage), as indicated by strong depletion of magmas in more to less incompatible elements (Sm/Yb < 0.8, Zr/Y < 2, Ti/V < 12) and high-Cr-spinel compositions (Cr# > 0.5). In comparison with Troodos boninites, the low-Ti Manihiki magmas had distinctively lower H2O contents (< 0.2 vs. > 2 wt% in boninites), ~ 100 °C higher liquidus temperatures at a given olivine Fo-number, lower fO2 (ΔQFM < + 0.2 vs. ΔQFM > + 0.2) and originated from deeper and hotter mantle (1.4–1.7 GPa, ~ 1440 °C vs. 0.8–1.0 GPa, ~ 1300 °C for Troodos boninites). The data provide new evidence that re-melting of residual upper mantle is not only restricted to subduction zones, where it occurs under hydrous conditions, but can also take place due to interaction of previously depleted upper mantle with mantle plumes from the deep and hotter Earth interior.  相似文献   

12.
Cu ± Au ± Mo mineralization is found in multiple intrusive suites in the Gangdese belt of southern Tibet (GBST). However, the petrogenesis of these ore-bearing intrusive rocks remains controversial. Here, we report on mineralization-related Late Cretaceous-early Eocene intrusive rocks in the Chikang–Jirong area, southern Gangdese. Zircon U–Pb analyses indicate that the mainly granodioritic Chikang and Jirong plutons were generated in the Late Cretaceous (ca. 92 Ma) and early Eocene (ca. 53 Ma), respectively. They are high-K calc-alkaline suites with high SiO2 (64.8–68.3 wt.%) and Al2O3 (15.1–15.7 wt.%) contents. Chikang granodiorites are characterized by high Sr (835–957 ppm), Sr/Y (118–140), Mg# (58–60), Cr (21.8–36.6 ppm), and Ni (14.3–22.9 ppm), and low Y (6.0–8.1 ppm), Yb (0.54–0.68 ppm) values with negligible Eu anomalies, which are similar to those of typical slab-derived adakites. The Jirong granodiorites have high SiO2 (64.8–65.3 wt.%) and Na2O + K2O (7.19–7.59 wt.%), and low CaO (2.45–3.69 wt.%) contents, Mg# (47–53) and Sr/Y (14–16) values, along with negative Eu and Ba anomalies. Both Chikang and Jirong granodiorites have similar εHf(t) (7.6–13.1) values. The Chikang granodiorites were most probably produced by partial melting of subducted Neo-Tethyan oceanic crust, and the Jirong granodiorites were possibly generated by partial melting of Gangdese juvenile basaltic crust. In combination with the two peak ages (100–80 and 65–41 Ma) of Gangdese magmatism, we suggest that upwelling asthenosphere, triggered by the rollback and subsequent break-off of subducted Neo-Tethyan oceanic lithosphere, provided the heat for partial melting of subducted slab and arc juvenile crust. Taking into account the contemporaneous occurrence of Gangdese magmatism and Cu ± Au ± Mo mineralization, we conclude that the Late Cretaceous–early Eocene magmatic rocks in the GBST may have a significant potential for Cu ± Au ± Mo mineralization.  相似文献   

13.
The effect of alkalis on the solubility of H2O and CO2 in alkali-rich silicate melts was investigated at 500 MPa and 1,250 °C in the systems with H2O/(H2O + CO2) ratio varying from 0 to 1. Using a synthetic analog of phonotephritic magma from Alban Hills (AH1) as a base composition, the Na/(Na + K) ratio was varied from 0.28 (AH1) to 0.60 (AH2) and 0.85 (AH3) at roughly constant total alkali content. The obtained results were compared with the data for shoshonitic and latitic melts having similar total alkali content but different structural characteristics, e.g., NBO/T parameter (the ratio of non-bridging oxygens over tetrahedrally coordinated cations), as those of the AH compositions. Little variation was observed in H2O solubility (melt equilibrated with pure H2O fluid) for the whole compositional range in this study with values ranging between 9.7 and 10.2 wt. As previously shown, the maximum CO2 content in melts equilibrated with CO2-rich fluids increases strongly with the NBO/T from 0.29 wt % for latite (NBO/T = 0.17) to 0.45 wt % for shoshonite (NBO/T = 0.38) to 0.90 wt % for AH2 (NBO/T = 0.55). The highest CO2 contents determined for AH3 and AH1 are 1.18 ± 0.05 wt % and 0.86 ± 0.12 wt %, respectively, indicating that Na is promoting carbonate incorporation stronger than potassium. At near constant NBO/T, CO2 solubility increases from 0.86 ± 0.12 wt % in AH1 [Na/(Na + K)] = 0.28, to 1.18 ± 0.05 wt % in AH3 [Na/(Na + K)] = 0.85, suggesting that Na favors CO2 solubility on an equimolar basis. An empirical equation is proposed to predict the maximum CO2 solubility at 500 MPa and 1,100–1,300 °C in various silicate melts as a function of the NBO/T, (Na + K)/∑cations and Na/(Na + K) parameters: \({\text{wt}}\% \;{\text{CO}}_{2} = - 0.246 + 0.014\exp \left( {6.995 \cdot \frac{\text{NBO}}{T}} \right) + 3.150 \cdot \frac{{{\text{Na}} + {\text{K}}}}{{\varSigma {\text{cations}}}} + 0.222 \cdot \frac{\text{Na}}{{{\text{Na}} + {\text{K}}}}.\) This model is valid for melt compositions with NBO/T between 0.0 and 0.6, (Na + K)/∑cation between 0.08 and 0.36 and Na/(Na + K) ratio from 0.25 to 0.95 at oxygen fugacities around the quartz–fayalite–magnetite buffer and above.  相似文献   

14.
As an important unconventional resource, oil shale has received widespread attention. The oil shale of the Chang 7 oil layer from Triassic Yanchang Formation in Ordos Basin represents the typical lacustrine oil shale in China. Based on analyzing trace elements and oil yield from boreholes samples, characteristics and paleo-sedimentary environments of oil shale and relationship between paleo-sedimentary environment and oil yield were studied. With favorable quality, oil yield of oil shale varies from 1.4% to 9.1%. Geochemical data indicate that the paleo-redox condition of oil shale’s reducing condition from analyses of V/Cr, V/(V + Ni), U/Th, δU, and authigenic uranium. Equivalent Boron, Sp, and Sr/Ba illustrate that paleosalinity of oil shale is dominated by fresh water. The paleoclimate of oil shale is warm and humid by calculating the chemical index of alteration and Sr/Cu. Fe/Ti and (Fe + Mn)/Ti all explain that there were hot water activities during the sedimentary period of oil shale. In terms of Zr/Rb, paleohydrodynamics of oil shale is weak. By means of Co abundance and U/Th, paleo-water-depth of oil shale is from 17.30 to 157.26 m, reflecting sedimentary environment which is mainly in semi deep–deep lake facies. Correlation analyses between oil yield and six paleoenvironmental factors show that the oil yield of oil shale is mainly controlled by paleo-redox conditions, paleoclimate, hot water activities, and depth of water. Paleosalinity and paleohydrodynamics have an inconspicuous influence on oil yield.  相似文献   

15.
采用电感耦合等离子体发射光谱和同位素质谱等测试方法,对泰国呵叻盆地中部二叠系浅海相碳酸盐岩进行了微量元素与碳氧同位素组成及指标分析,讨论了研究区二叠系沉积古环境及其与碳酸盐岩烃源岩发育的控制关系。通过δ~(13)C/δ~(18)O指标及Sr/Ba、V/Ni、V/(V+Ni)比值等综合判别表明,研究区二叠系帕诺考组碳酸盐岩浅水斜坡亚相以淡-微咸水为主,属弱氧化-弱还原环境。深水斜坡亚相位于浪基面以下,以半咸水-咸水为主,属于缺氧的还原环境,为有机质保存提供了有利条件,是研究区碳酸盐岩烃源岩发育的有利相带。  相似文献   

16.
上奥陶统-下志留统烃源岩是中国南方海相4套主力区域烃源岩之一,有关它形成与发育环境的研究是南方海相油气成藏理论的基础性问题.本文选择中上扬子南缘2条代表性剖面,对上奥陶统-下志留统沉积岩进行了详细的地球化学分析,提取其中对沉积古环境有指示意义的地化指标,对该段地层的古环境进行了恢复.研究表明,优质烃源岩段主要集中在上奥陶统五峰组和下志留统龙马溪组底部,V/(V+Ni)、Ni/Co、Ceanom、δEu和δ13Corg等地球化学指标与有机碳含量均有较好的相关性,这些指标的异常均表明优质烃源岩发育于缺氧环境.而龙马溪组上部地层的有机碳含量较低,各种地球化学指标也显示,此时缺氧环境遭到了破坏,这与当时的沉积环境多为高能环境、不利于烃源岩发育是一致的.  相似文献   

17.
The Yamansu belt,an important tectonic component of Eastern Tianshan Mountains,of the Central Asian Orogenic Belt,NW China hosts many Fe-(Cu)deposit.In this study,we present new zircon U-Pb geochronology and geochemical data of the volcanic rocks of Shaquanzi Formation and diorite intrusions in the Yamansu belt.The Shaquanzi Formation comprises mainly basalt,andesite/andesitic tuff,rhyolite and sub-volcanic diabase with local diorite intrusions.The volcanic rocks and diorites contain ca.315-305 Ma and ca.298 Ma zircons respectively.These rocks show calc-alkaline affinity with enrichment in large-ion lithophile elements(LILEs),light rare-earth elements(LREEs),and depletion in high field strength elements(HFSEs)in primitive mantle normalized multi-element diagrams,which resemble typical back-arc basin rocks.They show depleted mantle signature with ε_(Nd)(t)ranging from+3.1 to +5.6 for basalt;+2.1 to+4.7 for andesite;-0.2 to+1.5 for rhyolite and the ε_(Hf)(t)ranges from-0.1 to +13.0 for andesites;+5.8 to +10.7 for andesitic tuffs.We suggest that the Shaquanzi Formation basalt might have originated from a depleted,metasomatized lithospheric mantle source mixed with minor(3-5%)subduction-derived materials,whereas the andesite and rhyolite could be fractional crystallization products of the basaltic magma.The Shaquanzi Formation volcanic rocks could have formed in an intracontinental back-arc basin setting,probably via the southward subduction of the Kangguer Ocean beneath the Middle Tianshan Massif.The Yamansu mineralization belt might have undergone a continental arc to back-arc basin transition during the Late Carboniferous and the intra-continental back-arc basin might have closed in the Early Permian,marked by the emplacement of dioritic magma in the Shaquanzi belt.  相似文献   

18.
The distribution of trace metals in active stream sediments from the mineralized Lom Basin has been evaluated. Fifty-five bottom sediments were collected and the mineralogical composition of six pulverized samples determined by XRD. The fine fraction (<?150 µm) was subjected to total digestion (HClO4?+?HF?+?HCl) and analyzed for trace metals using a combination of ICP-MS and AAS analytical methods. Results show that the mineralogy of stream sediments is dominated by quartz (39–86%), phyllosilicates (0–45%) and feldspars (0–27%). Mean concentrations of the analyzed metals are low (e.g. As?=?99.40 µg/kg, Zn?=?573.24 µg/kg, V?=?963.14 µg/kg and Cr?=?763.93 µg/kg). Iron and Mn have significant average concentrations of 28.325 and 442 mg/kg, respectively. Background and threshold values of the trace metals were computed statistically to determine geochemical anomalies of geologic or anthropogenic origin, particularly mining activity. Factor analysis, applied on normalized data, identified three associations: Ni–Cr–V–Co–As–Se–pH, Cu–Zn–Hg–Pb–Cd–Sc and Fe–Mn. The first association is controlled by source geology and the neutral pH, the second by sulphide mineralization and the last by chemical weathering of ferromagnesian minerals. Spatial analysis reveals similar distribution trends for Co–Cr–V–Ni and Cu–Zn–Pb–Sc reflecting the lithology and sulphide mineralization in the basin. Relatively high levels of As were concordant with reported gold occurrences in the area while Fe and Mn distribution are consistent with their source from the Fe-bearing metamorphic rocks. These findings provide baseline geochemical values for common and parallel geological domains in the eastern region of Cameroon. Although this study shows that the stream sediments are not polluted, the evaluation of metal composition in environmental samples from abandoned and active mine sites for comparison and environmental health risk assessment is highly recommended.  相似文献   

19.
The Marahiq area represents a portion of the Pan-African belt from the Neoproterozoic age in south Egypt and includes metamorphosed ultramafic rocks, metavolcanic rocks, and granodiorite pluton. The area is characterized by the ancient abandoned Au mine and the recent active talc mines. The present paper provides a preliminary assessment of stream sediments for gold (Au) placer and environmental hazard. Steam sediments from 36 stations were analyzed using ICP-MS for determining the concentration of 53 elements. Various statistical techniques, graphical representations, a set of complementary sediment quality assessment methods, and different mapping methods have been applied. The results showed that Au and the investigated elements were influenced by long history of the ancient mining activities and weathering processes, leading to elevate Au and some heavy metal(loid)s concentrations and exhibit enrichment ratios as follows: Te > As > Au > Cu > Cd > Co > Ni > V. Whereas Cd, Co, and V were attributed to geogenic origin, As, Au, Cu, Ni, and Te were derived from anthropogenic mining activities. It is found that the anomalies of Au and the element of interest are indicative of Au placer and point out a new perspective Au-sulfide mineralization hosted along the favorable tectonic zones that were the main source of Au placer. Both As and Te are good pathfinders to explore Au placer and related mineralization. Environmentally, the excess of As, Cu, Ni, and Te could generate moderate levels of contamination and low level of ecological risk in the sediments. Although As, Cu and Ni posed medium–low potentially adverse effects and low toxicity levels, they cannot cause harmful influences on biological life. Accordingly, streambed sediments are considered as safe and acceptable as inoffensive materials for environmental management. Overall, this study is as reference values for governmental organizations for appraising future environmental pollution in the area. Also, it is fruitful for Au placer and promising with success for Au exploration along the shear zones and strike-slip faults.  相似文献   

20.
湘西北下寒武统黑色岩系是中国南方下寒武统黑色岩系的重要组成部分,富含钒镍钼等多金属元素。文中对湘西北下寒武统黑色岩系钒镍钼矿进行了微量元素研究,研究区内Ni、Cd、Mo、Sb、V、Zn、W、Ba等元素特别富集,高含量的Sb和Ba表明其为热水沉积;Mo含量极高说明其为缺氧的还原环境;高的V/（V+Ni）、V/Cr、Ni/Co以及δU值表明其沉积环境为缺氧环境;高的 U/Th表明本区有热水沉积作用;稀土元素配分模式、Ce和Eu异常及La/Yb Ce/La和La/Yb ΣREE图解投点表明其沉积环境为还原环境,并有热水沉积作用。可见黑色岩系形成于缺氧环境,热液活动为其提供了丰富的热液来源。  相似文献   

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