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1.
The Eocene Farim‐Saliquinhé phosphate mineralization (FSPM) is a buried sedimentary deposit located in the northern part of Guinea‐Bissau, discovered and spatially constrained during the 1980s by the French Geological Survey (BRGM). In the present work some of the data collected at that time are reworked in the framework of the development of a 3D geological and geochemical model of this mineralization. We show the usefulness of two classical multivariate statistical methods – principal component analysis (PCA) and cluster analysis (CA) – applied to eight geochemical variables (P2O5, SiO2, Al2O3, Fe2O3, CaO, MgO, F and CO2) measured in 247 samples from phosphate facies, for differentiation of samples taken from the different phosphate facies recognized in the FSPM, namely the main ore FPA (30 to 35% high grade phosphate), the calcareous low grade phosphate FPB (10 to 20% P2O5) (both Lutetian), and a mineralized Upper Eocene to Lower Oligocene cover (mainly including the FPO level and a silico‐aluminous phosphate bed), overlying the FPA, which can also be considered a third set of phosphate facies associated with the FSPM.  相似文献   

2.
Paléocène-Early Eocene phosphate outcrop in the Ras-Draâ deposit (Tunisia) comprises alternances of P-rich strata (P2O5 ≥ 18%) and P-poor ones (P2O5 ≤ 2%). In phosphate rich strata, P is concentrated in rounded grains—so-called pellets—(28% ≤ P2O5 ≤ 38%) embedded in a matrix—so-called exogangue—much poorer in P (P2O5 # 7%) than pellets. The study of pellets (whose size lies mainly between 100 and 500 μm), of their surrounding matrix and of poorly phosphatic sediments, interlayered between the phosphatic strata, has been performed by optical microscopy and various chemical analyses, ICP-AES (Inductively Coupled Plasma-Atomic Emission Spectroscopy) and punctual chemical analyses by EDS (Energy Dispersive Spectroscopy). Mineralogical and chemical studies of the Tunisian phosphatic pellets show that the basic mineralogical component of these grains is carbonate-fluor-apatite, or francolite. The structural formula of a representative specimen of francolite in the basin is as follows: (Ca4.63Mg0.13Na0.22)(PO4)2.51(CO3)0.48(OH0.77F0.23). The mineralogy of the constituents of the sediment surrounding pellets comprises carbonates, clays, silica (opal, quartz). Microscopic observations of Ras-Draâ phosphorites, added to geochemical results, establish that pellets are small bodies, allochtonous to their matrix and whose composition is independent of that of this matrix. Fecal cylindrical bodies and subspherical pellets, the latest being supposed to proceed from the fecal bodies by fragmentation, are considered to have been formed by fishes, as P-rich and organic matter-rich faeces. These faeces turn out to be resistant to mechanical dispersion and to chemical diffusion of soluble elements from and in direction of sea water. This closeness is responsible for the strong reducing conditions having prevailed inside and during the pellets diagenesis.  相似文献   

3.
Marine sedimentary phosphorites of Eocene age (Upper Ypresian) are exposed in the extreme west of Iraq within the Dammam Formation. They are associated with limestone and chert, and their deposition seems to have taken place in a shallow marine environment within a structurally controlled basin open to the sea from the northern and western sides only.The studied phosphorites are granular in texture, coarse-grained and cemented by calcite which is occasionally silicified. Bone fragments are present in small amounts. Carbonate-fluorapatite is the only phosphate mineral detected in these phosphorites, with relatively high amounts of the components SO4?2, CO3?2, F?1, H3O1 and Na1 substituting in the crystal structure.The Lower Eocene phosphorites of Iraq are part of the Tethyan phosphorite province, and are comparable in many aspects with those of Paleocene and Upper Cretaceous age in the Western Desert of the country.  相似文献   

4.
Many (bio)geochemical processes that bring about changes in sediment chemistry normally begin at the sediment-water interface, continue at depth within the sediment column and may persist throughout the lifetime of sediments. Because of the differential reactivity of sedimentary phosphate phases in response to diagenesis, dissolution/precipitation and biological cycling, the oxygen isotope ratios of phosphate (δ18OP) can carry a distinct signature of these processes, as well as inform on the origin of specific P phases. Here, we present results of sequential sediment extraction (SEDEX) analyses combined with δ18OP measurements, aimed at characterizing authigenic and detrital phosphate phases in continental margin sediments from three sites (Sites 1227, 1228 and 1229) along the Peru Margin collected during ODP Leg 201. Our results show that the amount of P in different reservoirs varies significantly in the upper 50 m of the sediment column, but with a consistent pattern, for example, detrital P is highest in siliciclastic-rich layers. The δ18OP values of authigenic phosphate vary between 20.2‰ and 24.8‰ and can be classified into at least two major groups: authigenic phosphate precipitated at/near the sediment-water interface in equilibrium with paleo-water oxygen isotope ratios (δ18Ow) and temperature, and phosphate derived from hydrolysis of organic matter (Porg) with subsequent incomplete to complete re-equlibration and precipitated deeper in the sediments column. The δ18OP values of detrital phosphate, which vary from 7.7-15.4‰, suggest two possible terrigenous sources and their mixtures in different proportions: phosphate from igneous/metamorphic rocks and phosphate precipitated in source regions in equilibrium with δ18Ow of meteoric water. More importantly, original isotopic compositions of at least one phase of authigenic phosphates and all detrital phosphates are not altered by diagenesis and other biogeochemical changes within the sediment column. These findings help to understand the origin and provenance of P phases and paleoenvironmental conditions at/near the sediment-water interface, and to infer post-depositional activities within the sediment column.  相似文献   

5.
Research on the Upper Campanian (Upper Cretaceous) Negev phosphorites (Mishash Formation), based on microprobe analyses, Fourier Transform Infrared spectroscopy, wet chemistry, microtextural (Scanning Electron Microscopy) studies and mineralogical analyses, together with quantified rates of sedimentation and P accumulation, enables the chemistry of these rocks to be better constrained across the Negev area and allows their suitability for the manufacture of P fertilizers to be better determined. Two phosphorite facies are differentiated: (i) a pristine phosphorite facies of low P content, more typical of basinal sections and (ii) a reworked, granular phosphorite facies commonly enriched in P, found predominantly near palaeo‐highs and forming most of the economic phosphates. The distribution of F/P2O5, CO2/F, U(IV), Cd, Zn and other trace metals (Mo, Ni, Cr, Cu, V and Y), rare‐earth elements concentration, Ce and Eu anomalies and heavy rare earth elements enrichment, are controlled by these two facies. F/P2O5 in carbonate‐fluorapatite is much lower (0·090 to 0·107) in the pristine than in the reworked facies (0·107 to 0·120); in addition, the lower F/P2O5 in the pristine facies is coupled with: (i) higher Cd, Zn, Mo, Ni, Cr, Cu and V concentrations; (ii) a considerably reduced (< 10%) U(IV) fraction of total U; (iii) lower rare earth elements/P2O5 and Y/P2O5 ratios; (iv) less negative Ce and Eu anomalies and lower heavy rare earth elements (Lu/La) enrichment; (v) an increase in Fe‐rich smectites in the clay fraction; and (vi) presence of OH in the carbonate‐fluorapatite structure. Sedimentary reworking of previously formed pristine phosphate, together with its redeposition near structural highs in more oxic bottom conditions, results in considerable diagenetic changes in the chemistry of the phosphorites, making them more suitable for economic exploitation. The results presented here provide geochemical criteria for identifying pristine phosphate in other phosphorite sequences and may help to better locate phosphate strata chemically suitable for the phosphate industry elsewhere.  相似文献   

6.
Phosphate deposits have been outlined in Falcón State (Northern Venezuela) and Táchira State (Southwestern Venezuela) using geochemical soil methods.The phosphate deposits located in Falcón State constitute lenses and masses interbedded with Tertiary limestone and shales. The area is covered by a thick soil with few outerops and the region is characterized by typical tropical rain forest. Soil samples taken every 1000 m across complete stratigraphic sequences were analyzed for P2O5 content. An anomalous area with a P2O5 content ranging from 3.19% to 9.04% was outlined accompanied by areas with less than 0.83% of P2O5. More than 11 million metric tons of commercial phosphatic rock were associated with this anomaly.In Táchira State several stratigraphic sequences of potentially phosphatic rocks with a thick cover of black soil were geochemically investigated. Soil samples taken each 10 m were analyzed for P2O5. A sequence of phosphatic rock was outlined showing a P2O5 content varying between 7.3% and 9.2%. Apparently the sequence is interbedded with phosphate-poor siliceous rocks showing a P2O5 content below 2%.As result of this preliminary investigation, expensive trenching, pitting and drilling works can be carefully planned.  相似文献   

7.
The content of major element oxides (Al2O3, SiO2, CaO, MgO, Fe2O3, P2O5, K2O, TiO2, and MnO) in soil surrounding the light metal factory (TLM), which was producing aluminium from 1937 till 1991, was investigated by EDXRF and XRD. The evaluation of a possible aluminium pollution linked to the industrial activity was studied by a comparison of soil around the TLM with control soil samples. Taking into account natural variations caused by bedrock lithology, control samples were taken in the soil developed upon the Upper Cretaceous limestones and Middle Eocene flysch deposits, while the TLM soil was sampled over the Upper Cretaceous and Early to Middle Eocene limestones; that way the samples constituted four groups, each containing five to seven samples. Control soil overlying flysch deposits differed strikingly from the other three groups by its increased CaO values, and decreased content of Al, Fe, Mn, and Ti-oxides, confirming the overall geochemical imprint of bedrock lithology on the analysed soils. However, a specific mineral composition (presence of alumina) of the TLM soil, together with peculiar correlations among Al2O3 and other oxides indicates a certain extent of aluminium pollution of the investigated area.  相似文献   

8.
The authors have studied an Albian glauconite—phosphate—carbonate ore in the Sierra de Espuña (Murcia), situated in the betic Cordilleras, nappe of Malaga. The geochemical data concern 76 samples from which the following elements were titrated by spectro-photometric methods: P, Fe, Ti, Al, Mg, Mn, Ca, Na, K, Zn, Li, Ni, Cr and Sr.The percentages of SiO2, P2O5, Al2O3, K2O and total Fe with respect to the insoluble fraction and the CaCO3, Mn, P2O5 amounts permit of partly explaining the phosphate—glauconite bond. The pH and Eh conditions, deduced from vertical variations in the chemistry, are associated with the mineralogic evolution of the glauconites.The authors define the paleoenvironment of this glauconite—phosphate ore deposit. They clearly separate the environment of the genesis from that of sedimentation of the grains. The sedimentation of carbonate—phosphate—glauconitic particles occurred in a confined environment without continental debris. These grains were formed in proximity of the shelf edge.The phosphate and carbonate supplies are attributed to upwelling of deep waters.  相似文献   

9.
Organic geochemical analysis, palynology, and PetroMod software for the organic matters of subsurface Tithonian to Valanginian Sulaiy formation of six wells in Basrah Region, South Iraq showed evidences for hydrocarbon generation potential. These analyses include quantitative studies such as pyrolysis, fluorescence spectroscopy, and total organic carbon (TOC), while the qualitative studies are the textural microscopy used in evaluating amorphous organic matter for palynofacies analysis leading to hydrocarbon assessments. High TOC content of up to 7.3 wt.%, kerogen type II of mesoliptinic type with hydrogen index of up to 466 mg HC/g TOC, and mature organic matter along with dysoxic–anoxic environment and stratigraphic framework have rated the succession as a source rock for oil with ordinate gas, not only in Iraq but also in neighboring Kuwait and Saudi Arabia. This case study is also inferred for hydrocarbon generation and expulsion by PetroMod software which confirmed the source potential.  相似文献   

10.
The contents of Li, V, P2O5, and Al2O3 in marls and mudstones collected from three different formations, cropping out in northern Iraq, showed that the ratios of Li/Al2O3, V/Al2O3, and P2O5/Al2O3 in these rocks can be used to discriminate environments of deposition of these formations. Relatively high values of the above ratios characterize the deep marine Shiranish environment while lowest values characterize freshwater environment of deposition of the Injana rocks. Despite that marls of the Fatha formation were deposited in marine lagoonal environment, the ratios P2O5/Al2O3 and V/Al2O3 could not be discriminated from the freshwater Injana mudstones. The well-known phenomenon that marine surface water and down to a depth of 50 m almost lacks soluble P explain this behavior. In such water, almost all the soluble P is consumed by surface organism rendering it unavailable for adsorption by the sediments. The high salinity of the lagoonal environment prevented adsorption of soluble V on clay minerals because of its inability to compete with other species of much higher concentrations.  相似文献   

11.
Separation of Mussorie rock phosphate (P2O5 = 20%) from Uttar Pradesh, India, containing pyrite, calcite and other carbonaceous impurities by flotation has been successfully attempted to upgrade the phosphate values. Based on Hallimond cell flotation results of single and synthetic mineral mixtures of calcite and apatite using oleic acid and potassium phosphate, conditions were obtained for the separation of calcite from apatite which is considered to be the most difficult step in the beneficiation of calcareous phosphates. Further studies using 250 g of the mineral (?60 +150 and ?150 mesh fractions, deslimed) in laboratory size Fagergren subaeration machine employed a stagewise flotation viz. carbonaceous materials using terpineol, pyrite using potassium-ethyl xanthate and calcite using oleic acid respectively. Separation was, however, found to be unsatisfactory in the absence of a depressant.Among starch, hydrofluosilicic acid and dipotassium hydrogen phosphate, which were tried as depressants for apatite in the final flotation stage, dipotassium hydrogen phosphate proved to be superior to others. However, the tests with the above fractions did not yield the required grade. This was possibly due to insufficient liberation of the phosphate mineral from the ore body and different experimental conditions due to scale up operations. Experiments conducted using ?200 mesh deslimed fractions has yielded an acceptable grade of 27.6% P2O5 with a recovery of about 60%. The results have been explained in terms of the specific adsorption characteristics of phosphate ions on apatite and the liberation size of the mineral.  相似文献   

12.
The paper presents the uranium (U) concentration and distribution pattern in the Paleoproterozoic phosphorites of Lalitpur district of Uttar Pradesh. The study of thin sections, SEM and XRD reveal that apatite is the essential phosphate mineral while quartz and feldspars are the dominant gangue in the phosphorites of the investigated area. The collophane is observed to be mostly oolitic in form and microspherulitic in texture. The major element geochemistry indicated that the phosphorite samples are rich in P2O5, CaO, SiO2 and Fe2O3 whereas depletion of MgO, MnO, K2O and Al2O3 was observed. The CaO/P2O5 ratio ranges from 1.13 to 1.46 which is slightly lower than that of cations and anions substituted francolite (1.621) and close to that of carbonate-fluorapatite (1.318). The trace element geochemistry indicates that the phosphorites of Lalitpur have the significant range of U concentration (1.67 to 129.67 μg/g) which is more than that of Th (0.69 to 0.09 μg/g) among the analysed trace elements in the phosphorite samples of the area. The positive correlation of U with P2O5, CaO and U/P2O5 indicates a close association of U with phosphate minerals like collophane (apatite), whereas negative correlation of U with SiO2 and Fe2O3 may be due to mutual replacement. The antipathetic relationship of U with Ni may be an indication of high oxidizing conditions, whereas sympathetic relationship of U with K2O points towards higher alkaline conditions of the basin of deposition during phosphatization. The variable concentration of U and its relationship with significant major and trace elements in most of the phosphorite samples lead one to believe that the deposition of these phosphorites might have taken place in highly alkaline medium during fairly oxidizing to weakly reducing environmental conditions of geosynclinal basin.  相似文献   

13.
In the basal section of the carbonates of the Maastrichtian Gramame Formation in the Pernambuco-Paraiba coastal basin of northeastern Brazil, major phosphate concentrations (P2O5 > 10%) were deposited in shallow-marine environments (inner shelf). In contrast, dolomite-associated phosphates are characterized by low P2O5 concentrations (<10%) and were deposited in the relatively deep water of a platform ramp, under conditions of limited oxygen availability. Calcite is the main carbonate phase remaining after the diagenesis that affected the phosphorite. A positive δ13C (up to +2%PDB), coupled with a positive MgO-δ180 correlation in the phosphate-enriched carbonates, suggests that upwelling currents were the early phosphogenic vectors during marine transgression, in contrast to warm superficial seawater that prevailed during the Maastrichtian elsewhere. The major phosphate concentrations are related to reworking and diagenesis in a shallow shelf environment during a regression pulse of sea level, followed by a dramatic drop of δ13C to negative values (down to ?6%PDB). This study suggests that carbon and oxygen isotopes can be used as potential tools for phosphorite prospecting elsewhere.  相似文献   

14.
The differences between the CO2 and O2 concentrations in soil air and atmospheric air have been measured where sulfide mineralization occurs beneath transported exotic overburden in semi-arid and arid areas of the USA, South West Africa (Namibia) and Saudi Arabia. These mineralizations are reflected near surface by anomalous levels of CO2 and O2 in soil air, whereas in most cases heavy-metal anomalies are absent. The normal background variability of CO2 and O2 in soil air falls with increasing aridity, and anomaly definition improves with increasing aridity. Thus soil air CO2 and O2 data are potentially useful in exploring for concealed mineralization, especially in regions with an arid climate or conspicuous dry season.  相似文献   

15.
The geochemistry and mineralogy of a condensed section, ~6 m thick of the West Kasrik member (Coniacian–Santonian) near the uplifted northern flank of the Mardin–Derik anticline (south-eastern Turkey) was studied. The only deposit exploited in Turkey is found in this area. The sediment textures as well as the mineralogical and the geochemical results collectively suggest that these recycled phosphorites accumulated in areas of intensive very early diagenesis of the sediments in highly oxic bottom waters, and almost no detrital apport. The total concentration of redox-sensitive trace metals is very low (<600 μg/g); in addition the structural CO2 and F/P2O5 are unusually high (~5 wt % and 0.14, respectively). REE distribution shows a clear “seawater” pattern with a strongly negative Ce-anomaly (0.20 ± 0.02) and heavy REE enrichment (LuN/LaN = 1.50 ± 0.12), however their total concentration is very low. The low REE contents, quite unexpected in recycled phosphorites, are explained by the scarcity of terrigenous components which leads to minimal incorporation of REEs from detrital clastic phases in the CFA fraction. Weathering previously suggested as responsible for the high P enrichment of the Mazidagi phosphorites is rather improbable in the samples we studied, in view of their high structural CO2, high F/P2O5, high (La/Nd)N and (La/Sm)N ratios, and high Sr/P and Ca/P of separated CFA fractions that all negate post-depositional weathering. More likely, the high P enrichment of some rocks (P2O5 content reaches 34%) was produced by sedimentary and early diagenetic processes acting in oxygenated areas of starved sedimentation on and around tectonic highs.  相似文献   

16.
Earthquakes in the Gulf of Aqaba were compiled from the Jordan Seismological Observatory bulletins, Saudi Arabia (SNSN, King Abdulaziz City for Science and Technology), and Egypt (National Research Institute of Astronomy and Geophysics, Helwan) sources and were relocated after reexamining the P and S arrival times, testing the efficiency of stations used to determine the location of Aqaba events, calculating the average value of V p/V s, and choosing the best crustal model for the study area. The earthquake epicenters are distributed along the eastern side of the Gulf of Aqaba.  相似文献   

17.
Northeast (NE) China is characterized by large areas of Mesozoic and Paleozoic granitoids, whereas Cenozoic granitoids are scarce. This paper reports LA-ICP-MS zircon U–Pb ages and whole-rock geochemical data for late Paleocene–early Eocene granitoids from the Jiamusi Massif, NE China, in order to determine their petrogenesis and tectonic implications. Geochronological data indicate that the granodiorite and dioritic porphyry from the Wudingshan pluton formed at 51.5 ± 0.3 Ma and 56.3 ± 0.8 Ma, respectively. The biotite–quartz diorite, biotite granodiorite, and dioritic porphyry have high SiO2 (68.38–70.06 wt.%), Al2O3 (15.34–15.79 wt.%), and Na2O (3.96–4.49 wt.%) contents, low MgO contents (1.10–1.26 wt.%), A/CNK ratios of 0.99–1.11, and are classified as medium- to high-K calc-alkaline and weakly peraluminous I-type granitoids. They are enriched in LREEs and LILEs, and depleted in HFSEs, with Nb/Ta ratios of 10.4–15.0. Moreover, they have negative Nb–Ta–Ti anomalies, indicating that they were derived from continental crust. Combining with the previously published isotopic data and regional geological results, we suggest that the late Paleocene–early Eocene granitoids (56–52 Ma) were probably derived from partial melting of juvenile lower crust, and formed in an active continental margin setting, possibly related to subduction slab rollback of the Paleo-Pacific Plate.  相似文献   

18.
《International Geology Review》2012,54(13):1641-1659
Eocene mafic volcanic rocks occurring in an E–W-trending, curvilinear belt along and north of the Izmir–Ankara–Erzincan suture zone (IAESZ) in northern Anatolia, Turkey, represent a discrete episode of magmatism following a series of early Cenozoic collisions between Eurasia and the Gondwana-derived microcontinents. Based on our new geochronological, geochemical, and isotope data from the Kartepe volcanic units in northwest Anatolia and the extant data in the literature, we evaluate the petrogenetic evolution, mantle melt sources, and possible causes of this Eocene volcanism. The Kartepe volcanic rocks and spatially associated dikes range from basalt and basaltic andesite to trachybasalt and basaltic trachyandesite in composition, and display calc-alkaline and transitional calc-alkaline to tholeiitic geochemical affinities. They are slightly to moderately enriched in large ion lithophile (LILE) and light rare earth elements (LREE) with respect to high-field strength elements (HFSE) and show negative Nb, Ta, and Ti anomalies reminiscent of subduction-influenced magmatic rocks. The analysed rocks have 87Sr/86Sr(i) values between 0.70570 and 0.70399, positive ?Nd values between 2.7 and 6.6, and Pb isotope ratios of 206Pb/204Pb(i) = 18.6–18.7, 207Pb/204Pb(i) = 15.6–15.7, and 208Pb/204Pb(i) = 38.7–39.1. The 40Ar/39Ar cooling ages of 52.7 ± 0.5 and 41.7 ± 0.3 Ma obtained from basaltic andesite and basalt samples indicate middle to late Eocene timing of this volcanic episode in northwest Anatolia. Calculated two-stage Nd depleted mantle model (TDM) ages of the Eocene mafic lavas range from 0.6 to 0.3 Ga, falling between the TDM ages of the K-enriched subcontinental lithospheric mantle of the Sakarya Continent (1.0–0.9 Ga) to the north, and the young depleted mantle beneath central Western Anatolia (0.4–0.25 Ga) to the south. These geochemical and isotopic features collectively point to the interaction of melts derived from a sublithospheric, MORB-like mantle and a subduction-metasomatized, subcontinental lithospheric mantle during the evolution of the Eocene mafic volcanism. We infer triggering of partial melting by asthenospheric upwelling beneath the suture zone in the absence of active subduction in the Northern Neotethys. The geochemical signature of the volcanic rocks changed from subduction- and collision-related to intra-plate affinities through time, indicating an increased asthenospheric melt input in the later stages of Eocene volcanism, accompanied by extensional deformation and rifting.  相似文献   

19.
The respective effects of phosphate modifiers on the solubility of calcium minerals in water, on the surface charge of the minerals and on the adsorption of the phosphates and of sodium oleate on the mineral surface were examined. The Auger spectra and the infrared spectra of the minerals treated with these reagents were also investigated. The ability of the phosphates to complex metal ions was determined by nephelometric titration. The structures of the minerals and their effects on their floatability, as well as structures of the phosphates and their effects on the complexation power were discussed. A mechanism of depression of the calcium minerals through the selective complexing dissolution of calcium ions from the mineral surface was derived and explains the higher selectivity obtained in scheelite flotation when (NaPO3)6 or Na4P2O7 are used as modifiers.  相似文献   

20.
Daraban Leucogranite dykes intruded discordantly into the basal serpentinized harzburgite of the Mawat Ophiolite, Kurdistan region, NE Iraq. These coarse grained muscovite-tourmaline leucogranites are the first leucogranite dykes identified within the Mawat Ophiolite. They are mainly composed of quartz, K-feldspar, plagioclase, tourmaline, muscovite, and secondary phologopite, while zircon, xenotime, corundum, mangano-ilemnite and cassiterite occur as accessories.The A/CNK value of the granite dyke samples varies from 1.10 to 1.22 indicating a strongly peraluminous composition. CaO/Na2O ranges from 0.11 to 0.15 and Al2O3/TiO2 from 264 to 463, similar to the strongly peraluminous (SP) granites exposed in ‘high-pressure’ collision zones such as the Himalayas.Ar–Ar muscovite step-heating dating yields 37.57 ± 0.25 and 38.02 ± 0.53 Ma plateau ages for two samples which are thought to reflect either their magmatic emplacement or resetting during collision-related metamorphism. Mineral chemistry shows evidence of both primary and secondary types of muscovite, with cores favouring the magmatic interpretation and slight effects of a late syn-serpentinization fluid seen at the rims.Geochemical features of Daraban Leucogranite dykes favour a syn-collisional tectonic setting. They probably formed in response to the continental collision between Eurasia and Arabia during the initial stage of the opening of the Gulf of Aden at 37 Ma. The muscovite ages and geochemical features of Daraban Leucogranite are strong evidence for the timing of the continental collision between northeastern Arabia and Eurasia in Kurdistan region of Iraq.  相似文献   

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