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1.
Detailed petrographic analyses along a depositional transect from a carbonate platform to shale basin reveals that dolomite is the principal burial diagenctic mineral in the Maryville Limestone. This study examines the role of burial dolomitization of subtidal carbonates. Dolomite occurs as a replacement of precursor carbonate and as inter- and intraparticle cements. Four different types of dolomite are identified based on detailed petrographic and gcochemical analyses. Type I dolomite occurs as small, irregular disseminations typically within mud-rich facies.Type II dolomite typically occurs as inclusions of planar euhedral rhombs (ferroan), 5–300 μm in size, in blocky clear ferroan calcite (meteoric) spar. Type II dolomite is non-luminescent. Type I and II dolomite formed during shallow to intermediate burial diagenesis. Type III dolomite consists of subhedral to anhedral crystals 10–150 μm in size occurring as thin seams along stylolites and as thick bands a few millimetres in width. This dolomite consists of dominantly non-luminescent rhombs and, less commonly, orange luminescent and zoned rhombs. Type IV dolomite consists of baroque or saddle-shaped, 100–1500 μm crystals, and is non-luminescent. Type IV dolomite formed during the period of maximum burial. Types III and IV dolomite increase in abundance downslope. Type III dolomite contains 1.2–2.6 wt% Fe and a maximum of 1000 ppm Mn. The distribution of these elements displays no distinct vertical or lateral trends. In contrast, Fe and Mn distributions in Type IV dolomite exhibit distinct spatial trends, decreasing from 3.5–4.5 wl% Fe and 0.1–0.3 wt% Mn in the west (slope/basin) to 1.5–2.5 wt% Fe and less than 600 ppm Mn in the east (shelf margin), a distance of approximately 60 km. Spatial trends in Fe and Mn distributions in Type IV saddle dolomite, suggest a west-east fluid flow during late burial diagenesis. Types III and IV dolomite have a mean δ18O value of - 7.8%00 and a mean δ13C value of + 1.1%00 (relative to the PDB standard). Based on a range of assumed basinal water composition of 2.8%00 SMOW, temperatures calculated from δ18O values of Types III and IV dolomite range between 75 and 160°C. 87Sr/86Sr data for Types III and IV dolomite range from 0.7111 to 0.7139. These values are radiogenic when compared to Cambrian marine values and are consistent with the presence of a diagenetic fluid that interacted with siliciclastic sediments. The distribution of Palaeozoic facies in the southern Appalachians indicates a Cambrian shale source for the fluids, whilst burial curves suggest a Middle Ordovician age for burial fluid movement.  相似文献   

2.
The diagenesis of carbonate platform sediments is controlled by the original facies and mineralogy, climate, sea-level changes and burial history; these controls are clearly seen in the diagenesis of the Urgonian platform carbonates of SE France. Early diagenesis in the Urgonian platform included the precipitation of marine cements, dissolution of rudist shells and minor karstification. Diagenetic features produced during this phase were controlled by several falls in relative sea-level during the Barremian to mid-Aptian punctuating platform sedimentation, the original mineralogy of the sediment and the prevailing semi-arid/arid climate in the region at this time. Following a relative sea-level rise and further sedimentation, progressive burial of the platform led to minor compaction, followed by precipitation of coarse, equant, zoned to non-luminescent, calcite cement. This cement was cut by later stylolites, suggesting a relatively shallow-burial origin. Stable isotope (mean values - 7.94%δ18O and 0.36%δ13C) and trace element (mean values of Fe 334 ppm, Mn 92 ppm and Sr 213 ppm) data suggest that these cements precipitated from meteoric fluids at temperatures slightly elevated relative to depositional temperatures. A variable thickness of replacive dolomite which occurs preferentially within the shelf-margin facies of the lower part of the Urgonian post-dates mechanical fracturing and chemical compaction, but pre-dates the main phase of stylolitization. It is probable that the dolomitizing fluid was sourced by the early compaction-driven release of connate fluids held within the underlying muddy units. The burial history of these rocks suggests that calcite cementation and dolomitization took place at relatively shallow burial depths (1–1.5 km). The overall diagenetic history of the Urgonian Limestone Formation is a reflection of the pre-conditioning of the platform limestones by climate, sea level, tectonics and the shallow burial depths experienced by the platform during the later Mesozoic.  相似文献   

3.
The Karoo volcanic sequence in the southern Lebombo monocline in Mozambique contains different silicic units in the form of pyroclastic rocks, and two different basalt types. The silicic units in the lower part of the Lebombo sequence are formed by a lower unit of dacites and rhyolites (67–80 wt.% SiO2) with high Ba (990–2500 ppm), Zr (800–1100 ppm) and Y (130–240 ppm), which are part of the Jozini–Mbuluzi Formation, followed by a second unit, interlayered with the Movene basalts, of high-SiO2 rhyolites (76–78 wt.%; the Sica Beds Formation), with low Sr (19–54 ppm), Zr (340–480 ppm) and Ba (330–850 ppm) plus rare quartz-trachytes (64–66 wt.% SiO2), with high Nb and Rb contents (240–250 and 370–381 ppm, respectively), and relatively low Zr (450–460 ppm). The mafic rocks found at the top of the sequence are basalts and ferrobasalts belonging to the Movene Formation. The basalts have roughly flat mantle-normalized incompatible element patterns, with abundances of the most incompatible elements not higher than 25 times primitive mantle. The ferrobasalt has TiO2  4.7 wt.%, Fe2O3t = 16 wt.%, and high Y (100 ppm), Zr (420 ppm) and Ba (1000 ppm). The Movene basalts have initial (at 180 Ma) 87Sr/86Sr = 0.7052–0.7054 and 143Nd/144Nd = 0.51232, and the Movene ferrobasalt has even lower 87Sr/86Sr (0.70377) and higher 143Nd/144Nd (0.51259). The silicic rocks show a modest range of initial Sr-(87Sr/86Sr = 0.70470–0.70648) and Nd-(143Nd/144Nd = 0.51223–0.51243) isotope ratios. The less evolved dacites could have been formed after crystal fractionation of oxide-rich gabbroic cumulates from mafic parental magmas, whereas the most silica-rich rhyolites could have been formed after fractional crystallization of feldspars, pyroxenes, oxides, zircon and apatite from a parental dacite magma. The composition of the Movene basalts imply different feeding systems from those of the underlying Sabie River basalts.  相似文献   

4.
Granulite grade marble layers interlayered with metapelitic granulites from Lützow Holm Bay, East Antarctica, provide insight into fluid–rock interactions during burial to and exhumation from lower crustal levels. Sub-millimeter scale strontium, oxygen and carbon isotope variations along with LA-ICPMS trace element geochemistry and mineral chemistry of texturally characterized carbonates and associated minerals helped to reconstruct the multistage metamorphic fluid history.Fluid–rock interaction dating back to prograde metamorphism are still preserved in consistently low oxygen and high strontium isotope compositions (δ18O = 12‰; 87Sr/86Sr(550Ma) = 0.7248) within a massif dolomitic marble layer that escaped significant later metasomatism. In most marbles, total re-crystallization and isotopic resetting occurred in the presence of “externally derived” hyper-saline fluids that circulated along the carbonate layers during the early stages of prograde metamorphism. This leads to a trend of increased radiogenic Sr in marbles towards the value of associated metapelitic rocks that have 87Sr/86Sr(550Ma) of 0.764.LA-ICPMS studies on trace elements in carbonate and associated silicate minerals at different textural settings, distinguished using cathodoluminescence microscopy, revealed multiple metasomatic events during retrograde metamorphism. Trace element contents of Ba, Sr, Pb and U gave compelling evidence for metasomatic alteration that postdate the exsolution of carbonate at ~ 600 ºC, which can be correlated with the fluids released from the crystallization of anatectic melts and pegmatites. Subsequently, meteoric fluid infiltration occurred at a shallower level of the crust and caused extreme oxygen isotopic heterogeneity (δ18O = 14.7 ~ ? 4.9‰) and imprinted high concentration of fluid mobile elements. Taken together our results emphasize the importance of integrating textural and chemical heterogeneities to reveal the multiple episodes of fluid–rock interaction processes in a dynamic continental crust, which has major implications on migration of fluids and material and help in formulating models on the geodynamic evolution of crust.  相似文献   

5.
The giant sediment-hosted Jinding zinc-lead deposit is located in the Lanping Basin, northwestern Yunnan Province, China. The genesis of the deposit has long been debated and the sources of the ore-forming fluids and metals are controversial. This study presents rare earth element (REE) and noble gas isotope data that constrain the origins of the ore fluids and the heat source driving the hydrothermal circulation. The early-stage sulfides are enriched in light REEs and have high ∑REE values (30.8–94.8 ppm) and weakly negative Eu (δEu 0.85–0.89) and Ce anomalies (δCe 0.84–0.95), suggesting that the fluids were likely derived from dissolution of Upper Triassic marine carbonates with input of REEs from aluminosilicate rocks in the basin. In contrast, the late-stage sulfides have irregular REE patterns, generally low ∑REE values (0.24–10.8 ppm) and positive Eu (δEu 1.22–10.9) and weakly negative Ce anomalies (δCe 0.53–0.90), which suggest that the ore-forming fluids interacted with evaporite minerals. The 3He/4He (0.01–0.04 Ra) and 40Ar/36Ar values (301–340) of the ore-forming fluids indicate crustal and atmospheric origins for these noble gases. These findings are in agreement with the published fluid inclusion microthermometry data and the results of H, O, C, S, Pb and Sr isotope studies. Our data, in combination with published results, support a two-stage hydrothermal mineralization model, involving early-stage basinal brines and late-stage meteoric water that acquired metals and heat from crustal sources.  相似文献   

6.
The Ebrahim-Attar (EBAT) leucogranite body is intruded within the Jurassic metamorphic complex of the Ghorveh area, located in the northern part of the Sanandaj Sirjan zone (SaSZ) of northwest Iran. The granite comprises alkali feldspar, quartz, Na-rich plagioclase and to a lesser extent, muscovite and biotite. Garnet and beryl are also observed as accessory minerals. Additionally, high SiO2 (71.4–81.0wt %) and Rb (145–440 ppm) content; low MgO (<0.12wt %), Fe2O3 (< 0.68 wt.%), Sr (mainly < 20 ppm), Ba (<57 ppm), Zr (10–53 ppm) and rare earth elements (REEs) low content (3.88–94.9 ppm with an average = 21.2 ppm); and flat REE patterns with a negative Eu anomaly characterize these rocks. The chemical composition and mineral paragenesis indicate that the rocks were formed by the partial melting of siliciclastic to pelitic rocks and can be classified as per-aluminous leucogranite or strongly per-aluminous (SP) granite. The Rb-Sr whole rock and mineral isochrons confirm that crystallization of the body occurred at 102.5 ± 6.1 Ma in Albian. The 87Sr/86Sr(i) and 143Nd/144Nd(i) ratios are 0.7081 ± 0.009 and 0.51220 ± 0.00005, respectively, and εNd(t) values range from −5.8 to −1.6. These values verify that the source of this body is continental crust. The Nd model ages (TDM2) vary between 1.0 and 1.3 Ga and are more consistent with the juvenile basement of Pan African crust. Based on these results, we suggest that the upwelling of the hot asthenospheric mantle in the SaSZ (likely during the Neo-Tethys rollback activity) occurred after the late Cimmerian orogeny. Consequently, we suggest that this process was responsible for a thinning and heating of the continental crust, from which the SP granite was produced by the partial melting of muscovite rich in pelitic or felsic-metapelitic rocks in the northern SaSZ.  相似文献   

7.
The Lanping basin is a significant Pb–Zn–Cu–Ag mineralization belt in the Sanjiang Tethyan metallogenic province. A series of sediment-hosted Himalayan Cu–Ag–Pb–Zn polymetallic deposits have been discovered in the western part of the basin, controlled by a thrust–nappe system. In the thrust–nappe system, the Cu orebodies mainly occur in the western and relatively deep part of the mineralization system (the root zone), whereas the Pb–Zn–Ag (± Cu) orebodies occur in the eastern and relatively shallow part of the system (the front zone), both as vein-type mineralization.In this paper we present new data, combined with existing data on fluid inclusions, isotopes and geologic characteristics of representative deposits, to provide the first study that contrasts mineralizing fluids in the Cu–Ag (Mo) and Pb–Zn–Ag (Cu) polymetallic deposits.Fluid inclusion and isotope studies show that the Cu–Ag (Mo) mineralization in the root zone formed predominantly from deep crustal fluids, with the participation of basinal brines. The deep crustal fluids are marked by high CO2 content, relatively high temperatures (280 to 340 °C) and low salinities (1 to 4 wt.% NaCl equivalent), whereas the basinal brine shows relatively low temperatures (160 °C to 220 °C) and high salinities (12 to 22 wt.% NaCl equivalent), containing almost no CO2. In comparison, hydrothermal activity associated with the Pb–Zn–Ag (± Cu) deposits in the front zone is characterized by basinal brine, with relatively low temperatures (130 °C to 180 °C), high salinities (9 to 24 wt.% NaCl equivalent), and low CO2 concentrations. Although evolved meteoric waters have predominantly been proposed as the source for deep crustal fluids, magmatic and metamorphic components cannot be completely excluded. The basinal brine was predominantly derived from meteoric water.The δ34S values of sulfides from the Cu–Ag (Mo) deposits and Pb–Zn–Ag (± Cu) deposits range from − 17.9 to 16.3‰ and from 2.5 to 11.2‰, respectively. These ranges may relate to variations in physicochemical conditions or compositional variation of the sources. Lead isotope compositions indicate that the ore-forming metals were predominantly derived from sedimentary rocks of the Lanping basin.  相似文献   

8.
Ore-forming porphyries and barren granitoids from porphyry Cu deposits differ in many ways, particularly with respect to their adakitic affinity and calc-alkaline characteristics. In this study, zircon U–Pb and molybdenite Re–Os dating, whole rock geochemistry, whole rock Sr–Nd–Pb and zircon O–Hf isotopic analyses were carried out on the ore-forming granitoids from the Kounrad, Borly and Sayak deposits, and also on pre-ore and post-ore granitoids in adjacent regions of Central Kazakhstan. Geochronology results indicate that pre-ore magmatism occurred in the Late Devonian to Early Carboniferous (361.3–339.4 Ma), followed by large scale Cu mineralization (325.0–327.3 Ma at Kounrad, 311.4–315.2 Ma at Borly and 309.5–311.4 Ma at Sayak), and finally, emplacement of the Late Carboniferous post-ore barren granitoids (305.0 Ma). The geochemistry of these rocks is consistent with calc-alkaline arc magmatism characterized by strong depletions in Nb, Ta and Ti and enrichments in light rare earth elements and large ion lithophile elements, suggesting a supra-subduction zone setting. However, the ore-forming rocks at Kounrad and Sayak show adakitic characteristics with high Sr (517.5–785.3 ppm), Sr/Y (50.60–79.26), (La/Yb)N (9.37–19.62) but low Y (6.94–11.54 ppm) and Yb (0.57–1.07 ppm), whereas ore-forming rocks at Borly and barren rocks from northwest of Borly and Sayak have normal arc magma geochemical features. The Sr–Nd–Hf–O isotopic compositions show three different signatures: (1) Sayak granitoids have very young juvenile lower crust-derived compositions ((87Sr/86Sr)i = 0.70384 to 0.70451, ɛNd (t) = + 4.9 to + 6.0; TDM2 (Nd) = 580 to 670 Ma, ɛHf (t) = + 11.3 to + 15.5; TDMC (Hf) = 330 to 600 Ma, δ18O = 6.0 to 8.1‰), and were probably generated from depleted mantle-derived magma with 5–15% sediment melt addition in the magma source; (2) the Kt-1 granite from northwest of Sayak shows extremely enriched Sr–Nd isotopic compositions ((87Sr/86Sr)i = 0.71050, ɛNd (t) =  7.8, TDM2 (Nd) = 1700 Ma), likely derived from partial melting of ancient continental crust; (3) other granitoids have transitional Sr–Nd compositions between the Sayak and Kt-1 samples, indicating a juvenile lower crust source with the addition of 10–30% of ancient crustal material. The pre-ore magmatism was probably related to partial melting of juvenile lower crust due to northward subduction of the Junggar–Balkhash Ocean, whereas the ore-forming adakitic rocks at Aktogai, Kounrad and Sayak formed by partial melting of thickened lower crust which subsequently delaminated. The ore-forming rocks at Borly, and the later post-ore barren granites, formed by partial melting of juvenile lower crust with normal thickness. This tectonic setting supports the existence of an Andean-type magmatic arc in the Devonian to the Late Carboniferous, resulting from the subduction of the Junggar–Balkhash oceanic plate. The link between whole rock geochemistry and scale of mineralization suggests a higher metallogenic potential for adakitic rocks than for normal arc magmatism.  相似文献   

9.
The Miao'ershan uranium ore district is one of the most important granite-hosted uranium producers in South China. There are several Triassic granite plutons in the Miao'ershan batholith, but uranium ore deposits mainly occur within the Douzhashan granitic body. Precise zircon U–Pb dating indicated that these Triassic granite plutons were emplaced during 204 to 215 Ma. The Douzhashan U-bearing granite lies in the central part of the Miao'ershan batholith, and has higher U contents (8.0 to 26.1 ppm, average 17.0 ppm) than the nearby Xiangcaoping granite (5.0 to 9.3 ppm, average 7.0 ppm) and the Yangqiaoling granite (6.4 to 18.3 ppm, average 11.5 ppm) in the south part of the batholith. The Douzhashan granite is composed of medium-grained two-mica granite, whereas the Xiangcaoping and Yangqiaoling granites are composed of porphyritic biotite granite. Both the Xiangcaoping and Douzhashan granites have high A/CNK ratios (> 1.10), high (87Sr/86Sr)i ratios (> 0.720) and low εNd(t) values (− 11.3 to − 10.4), suggesting that they belong to strongly peraluminous S-type granites. The Douzhashan granite has low CaO/Na2O ratios, high Rb/Sr and Rb/Ba ratios, indicating a partial melting origin of clay-rich pelitic rocks. In contrast, the Xiangcaoping granite formed from clay-poor psammite-derived melt. The Yangqiaoling granite shows different geochemical characteristics with the Douzhashan and Xiangcaoping granites, indicating a different magma source. The Yangqiaoling granite has higher εNd(t) of − 9.4 to − 8.3 and variable A/CNK values from 0.98 to 1.19, suggesting a mixture source of meta-sedimentary rocks and meta-igneous rocks. Crystallization fractionation is not the main mechanism for U enrichment in the Douzhashan granite. We suggest that U-rich pelitic rock sources may be the key factor to generate peraluminous U-bearing granites in South China. Searching for those granites which are reduced, strongly peraluminous and were derived from U-rich pelitic rocks, is the most effective way for exploring granite-hosted U deposits.  相似文献   

10.
The Upper Cretaceous Nakhlak epigenetic vein-type Pb(Ag) deposit is located 55 km northeast of the town of Anarak in Isfahan Province, Iran. The deposit contains 7 Mt of galena-barite ore with an average grade of 8.33% Pb, 0.38% Zn, and 72 ppm Ag. The ore mineralization occurs as stratabound, epigenetic, steeply dipping, east-west–trending veins in faulted- or fracture-controlled Upper Cretaceous Sadar carbonates. Galena and barite are the primary minerals. Minor sphalerite, tennantite-tetrahedrite, pyrite, and chalcopyrite occur as inclusions in galena. Cerussite with minor amounts of anglesite and plattnerite formed in the oxidized supergene zone. The ore and ore-related minerals were deposited in the hydrothermally dolomitized carbonate host rock containing saddle-shaped dolomite. Geochemically, the dolomitized carbonate host rocks are enriched in MgO, Fe2O3, MnO, Pb, Zn, and Ba, but depleted in CaO. The galena concentrate contains high values of Ag (932 ppm), Sb (342 ppm), Cu (422 ppm), As (91 ppm), and Zn (296 ppm); the presence of these trace elements indicates a low-temperature type of galena mineralization. This interpretation is corroborated by fluid inclusions containing 12.98 wt.% NaCl equivalent salinity; the inclusions homogenize at the low temperature of about 152.1 °C. The similarity between δ34S(V-CDT) values in Nakhlak barite and Permian–Triassic δ34S marine sulfate values indicates that the Nakhlak sulfur was probably provided from evaporates of Permian–Triassic age. The δ34S(V-CDT) values of galena and barite samples occupy the ranges of − 1.04‰ to + 8.62‰ and + 10.95‰ to + 13.71‰, respectively, and are similar to Mississippi Valley–type (MVT) deposits. The low-temperature basinal fluids, evaporate-originated sulfur, and fault- or fracture-controlled galena-rich veins in the Nakhlak deposit resemble the type of geological features documented in Pb-rich MVT deposits.  相似文献   

11.
The Xishan deposit, located in the western Guangdong Province in South China, is a quartz-vein type W-Sn deposit with an average Sn grade of 0.1–0.4 wt%. The deposit is temporally and spatially associated with Xishan alkali feldspar granite. The W–Sn mineralization is present mainly as veins that are hosted by the granite. In this paper we present new zircon U–Pb age, whole-rock geochemical data, Sr–Nd–Pb–Hf isotopic data and Re–Os age in order to constrain the nature and timing of magmatism and mineralization in the Xishan mining district with implications on geodynamic settings. LA–ICP–MS zircon U–Pb analyses yielded an age of 79.14 ± 0.31 Ma for the alkali feldspar granite, consistent with the molybdenite Re–Os age of 79.41 ± 1.11 Ma. The alkali feldspar granite shows high contents of SiO2 (71.52–76.25 wt%), high total alkalis (Na2O + K2O = 9.35–13.51 wt%), high field strength elements (e.g. Zr = 95.4–116 ppm, Y = 97.1–138 ppm, Nb = 36.1–55.5 ppm, Ga = 97.1–138 ppm), and rare earth elements (total REE = 171.8–194.0 ppm) as well as high Ga/Al ratios (10,000 × Ga/Al = 3.23–3.82) suggesting that it has the geochemical characteristics of A-type granite and shows an A2 subtype affinity. Sr–Nd isotopes of the alkali feldspar granite show that (87Sr/86Sr)i values range from 0.7111 to 0.7183, and the εNd(t) values and Nd model ages (T2DM) vary from −6.8 to −6.5 and 1414 to 1433 Ma, respectively. The Pb isotopic compositions are variable, with 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb values ranging from 18.783 to 18.947, 15.709 to 15.722 and 38.969 to 39.244, respectively, indicating that the alkali feldspar granite was derived from a mantle-crust mixed source. In situ Hf isotopic analyses reveal that the alkali feldspar granite has εHf(t) values ranging from −9.69 to −0.04 and two-stage Hf model ages from 1145 Ma to 1755 Ma, indicating that the alkali feldspar granite was formed by the partial melting of Mesoproterozoic crusts of the Cathaysia Block with additions of mantle-derived materials. These results, together with previously presented regional geological relationships, suggest that the formation of the Xishan granite and associated W–Sn mineralization is related to lithospheric extension and asthenospheric upwelling that are attributed to a directional change of Pacific plate motion.  相似文献   

12.
《Gondwana Research》2014,25(3-4):1108-1126
Detailed petrology and zircon U–Pb dating data indicate that the Wulong pluton is a zoned granitic intrusive, formed from successive increments of magmas. An age range of at least 30 Ma is recorded from the 225–235 Ma quartz diorite on the pluton margin, the ca. 218 Ma granodiorite in the intermediate zone, and the ca. 207 Ma monzogranite at the pluton center. All the granitoids display evolved Sr–Nd–Pb isotopic compositions, with 87Sr/86Sr(i) of 0.7044–0.7062, unradiogenic Nd (εNd(t) values of − 6.1 to − 3.0, Nd model ages of 1.1–1.3 Ga, and moderately radiogenic Pb compositions (206Pb/204Pb(i) = 17.500–17.872, 207Pb/204Pb(i) = 15.513–15.549, 208Pb/204Pb(i) = 37.743–38.001), in combination with variations in zircon Hf isotopic compositions (with εHf(t) values in each stage span 12 units) and the Hf isotopic model ages of 800–1600 Ma. These features suggest that the granitoids might have been derived from the reworking of an old lower crust, mixed with Paleozoic and Proterozoic materials. The rocks also display an adakitic affinity with Sr (479–973 ppm), high Sr/Y ratios (mostly > 60) and negligible Eu anomalies (Eu/Eu* = 0.78–0.97) but low Rb/Sr ratios, low Y (4.6–17 ppm), HREE (Yb = 0.95–1.7 ppm), Yb/Lu (6–7) and Dy/Yb (1.9–2.4) ratios, suggesting the absence of plagioclase and presence of garnet + amphibole in their residue. Considering a large gap among their crystallization ages, we propose that the geochemical evolution from pluton margin to center was controlled mainly by melting conditions and source compositions rather than fractional crystallization. Mafic enclaves that were hosted in the quartz diorite and granodiorite are mainly syenogabbroic to syenodioritic in composition, and are metaluminous and enriched in LREE and LILEs, but are depleted in HFSE, and display an evolved Sr–Nd–Pb isotopic composition, suggesting that they may have been derived from the partial melting of an enriched mantle lithosphere, which was metasomatized by adakitic melts and fluids from a subducted continental crust.In combination with the results of the Triassic ultra-high pressure metamorphic rocks in the Dabie orogenic belt, we apply a model involving the exhumation of subducted continental crust to explain the formation of the Wulong pluton. At the first stage, a dense and refractory mafic lower crust that was trapped at mantle depth by continental subduction witnessed melting under high temperature conditions to produce the quartz diorite magma, characterized by low SiO2 (60.65–63.98 wt.%) and high TiO2 (0.39–0.86 wt.%). The magma subsequently interacted with mantle peridotite, leading to high Mg# (57–67) and the metasomatism of the overriding mantle wedge. At the second stage, an asthenosphere upwelling that was probably caused by slab break-off at ca. 220 Ma melted the enriched sub-continental lithospheric mantle (SCLM) to produce mafic magmas, represented by the mafic enclaves that are hosted in the quartz and granodiorite, resulting in the partial melting of the shallower subducted crust, and generating the granodiorite that is distinguished by high SiO2 (69.16–70.82 wt.%), high Al2O3 (15.33–16.22 wt.%) and A/CNK values (mostly > 1.05). At the third stage, the final collapse of the Triassic Qinling–Dabie Orogenic Belt at ca. 215–205 Ma caused extensive partial melting of the thickened orogenic lower crust to produce the monzogranite, which is characterized by high SiO2 (67.68–70.29 wt.%), low TiO2 (mostly < 0.35 wt.%) and high Sr/Y ratios of 86–151.  相似文献   

13.
The Eocene (ca. 55–38 Ma) Bear Lodge alkaline complex in the northern Black Hills region of northeastern Wyoming (USA) is host to stockwork-style carbonatite dikes and veins with high concentrations of rare earth elements (e.g., La: 4140–21000 ppm, Ce: 9220–35800 ppm, Nd: 4800–13900 ppm). The central carbonatite dike swarm is characterized by zones of variable REE content, with peripheral zones enriched in HREE including yttrium. The principle REE-bearing phases in unoxidized carbonatite are ancylite and carbocernaite, with subordinate monazite, fluorapatite, burbankite, and Ca-REE fluorocarbonates. In oxidized carbonatite, REE are hosted primarily by Ca-REE fluorocarbonates (bastnäsite, parisite, synchysite, and mixed varieties), with lesser REE phosphates (rhabdophane and monazite), fluorapatite, and cerianite. REE abundances were substantially upgraded (e.g., La: 54500–66800 ppm, Ce: 11500–92100 ppm, Nd: 4740–31200 ppm) in carbonatite that was altered by oxidizing hydrothermal and supergene processes. Vertical, near surface increases in REE concentrations correlate with replacement of REE(±Sr,Ca,Na,Ba) carbonate minerals by Ca-REE fluorocarbonate minerals, dissolution of matrix calcite, development of Fe- and Mn-rich gossan, crystallization of cerianite and accompanying negative Ce anomalies in secondary fluorocarbonates and phosphates, and increasing δ18O values. These vertical changes demonstrate the importance of oxidizing meteoric water during the most recent modifications to the carbonatite stockwork. Scanning electron microscopy, energy dispersive spectroscopy, and electron probe microanalysis were used to investigate variations in mineral chemistry controlling the lateral complex-wide geochemical heterogeneity. HREE-enrichment in some peripheral zones can be attributed to an increase in the abundance of secondary REE phosphates (rhabdophane group, monazite, and fluorapatite), while HREE-enrichment in other zones is a result of HREE substitution in the otherwise LREE-selective fluorocarbonate minerals. Microprobe analyses show that HREE substitution is most pronounced in Ca-rich fluorocarbonates (parisite, synchysite, and mixed syntaxial varieties). Peripheral, late-stage HREE-enrichment is attributed to: 1) fractionation during early crystallization of LREE selective minerals, such as ancylite, carbocernaite, and Ca-REE fluorocarbonates in the central Bull Hill dike swarm, 2) REE liberated during breakdown of primary calcite and apatite with higher HREE/LREE ratios, and 3) differential transport of REE in fluids with higher PO43−/CO32− and F/CO32− ratios, leading to phosphate and pseudomorphic fluorocarbonate mineralization. Supergene weathering processes were important at the stratigraphically highest peripheral REE occurrence, which consists of fine, acicular monazite, jarosite, rutile/pseudorutile, barite, and plumbopyrochlore, an assemblage mineralogically similar to carbonatite laterites in tropical regions.  相似文献   

14.
The Beiligaimiao magmatic Ni-Cu sulfide deposit is located in the northern rim of the North China Block, which was an active continental margin related to the southward subduction of the Paleo-Asian oceanic plate to the north in the Paleozoic. This deposit has never been studied before but is an excellent example of sulfide mineralization in arc settings that have been commonly overlooked by exploration geologists worldwide. Sulfide mineralization in the deposit is hosted in a mafic-ultramafic complex that consists of a small ultramafic body surrounded by an older and much larger gabbroic intrusion. Disseminated sulfide zones are present in both intrusive bodies but only those close to the surface within the ultramafic body have been mined in the past. The sulfide-mineralized ultramafic body is composed of olivine websterite and orthopyroxenite with a gradational contact between them. SIMS U-Pb dating of zircon crystals from a large olivine websterite sample yields a crystallization age of 269.4 ± 2.1 Ma, which is ∼25 Ma younger than the Erbutu subduction-related magmatic Ni-Cu sulfide deposit that occurs ∼50 km to the north. Orthopyroxene crystals in the Beiligaimiao ultramafic rocks have Mg# [100 Mg/(Mg + Fe), molar] of 77–78, significantly lower than those in the ultramafic rocks of the Erbutu deposit. Olivine crystals in the Beiligaimiao ultramafic rocks have forsterite (Fo) contents from 72 to 75 mol%, which are also significantly lower than those in the ultramafic rocks of the Erbutu deposit (Fo, 86–88 mol%). The mineral chemical data indicate a more fractionated parental magma for the former. Ca-depletion in olivine (i.e., <1000 ppm Ca), which is common for ultramafic cumulates in arc settings worldwide, is present in both deposits. Like Erbutu, the host rocks of the Beiligaimiao deposit are characterized by enrichments in light rare earth elements (REE) relative to heavy REE and pronounced negative Nb-Ta anomalies, consistent with ultramafic rocks in arc settings. The δ34S values of sulfide separates from the Beiligaimiao deposit are 1.7 to 2.5‰, significantly lower than those for the Erbutu deposit but still slightly higher than the MORB value (−1.5 to 0.5‰). Olivine websterites in the Beiligaimiao deposit have εNd from −8.9 to −9.5 and (87Sr/86Sr)i close to 0.7075, which are similar to those of an enriched lithospheric mantle. An orthopyroxenite sample from the deposit has much lower εNd (−12.6) coupled with much higher (87Sr/86Sr)i ratio (0.7132), indicating ∼25% crustal contamination. The Sr-Nd-S isotope data support the premise that both crustal contamination and addition of crustal sulfur played a role in triggering sulfur saturation in the parental magma of the Beiligaimiao deposit. Since the immediate country rocks are exclusively gabbros, these processes likely took place at depth. The close temporal and spatial association of the Beiligaimiao and Erbutu deposits points to the possibility that more Permian arc-type magmatic sulfide deposits are yet to be discovered in the region.  相似文献   

15.
The unconformity-type uranium deposits of the Athabasca Basin (Saskatchewan, Canada) are hosted near the unconformity between a middle Proterozoic intracratonic sedimentary basin and an Archean to Paleo-Proterozoic metamorphic and plutonic basement. These deposits, which are considered to be the richest U deposits in the world, are the result of massive basinal fluid migrations in the basement rocks.This study shows that basinal brines have strongly penetrated into the basement not only through faults and major pathways but also by way of dense networks of microfractures which favoured the percolation of fluids down to considerable depths (hundred metres below the unconformity) and their chemical modification (salinity increase) by interaction with basement lithologies. These processes are one of the major causes of uranium mobility within the basement rocks and the formation of unconformity-type mineralization.Microfracture networks, which opened during the basinal brine stage (ca. 1600–1400 Ma) are interpreted as sets of mode I cracks corresponding to a specific stage of deformation and occur as fluid inclusion planes after healing. The stress field at that stage (σ1 = N130–150 °E, subvertical) partly reopened the earlier microcrack networks (σ1 = N80–110 °E and N130–150 °E, subvertical) issued from the Trans-Hudson Orogeny late retrograde metamorphic stage (ca. 1795–1720 Ma). The circulation of the two types of fluids (carbonic and brines) occurs thus at two distinct events (Trans-Hudson Orogeny late retrograde metamorphism for carbonic fluids and maximal burial diagenesis for brines) but the same main microfissure geometry was used by the fluids. This demonstrates the existence of a similar stress field direction acting before and after the basin formation. Moreover, the brine circulations in the basement acted in a wider volume than the clay-rich alteration halo surrounding the U-ores, generally considered as the main envelope of fluid percolation outside the fault systems. The data on the chemistry of the fluids and on the geometry of their migration at various scales emphasise the fundamental role of the basement in the chemical evolution of highly saline brines linked to unconformity-related uranium mineralization in the Athabasca Basin.  相似文献   

16.
Through detailed studies we have delineated a suite of banded TTG gneisses from the Zanhuang Complex. The protolith of the gneisses, predominantly tonalite, has undergone intensive metamorphism, deformation and anatexis and in a banded structure is intimately associated with melanocratic dioritic gneiss and leucocratic trondhjemitic veins. SHRIMP Zircon U–Pb data show that the tonalite was formed ca. 2692 ± 12 Ma ago. The tonalitic gneiss has the features of high SiO2 (67.76–73.31%), high Al2O3 (14.38–15.83%), rich in Na2O (4.48–5.07%) and poor in K2O (0.77–1.93%). The gneiss is strongly fractioned in REE ((La/Yb)N = 12.02–24.65) and shows a weak positive Eu anomaly (Eu/Eu* = 1.05–1.64). It has high contents of Ba (199–588 ppm) and Sr (200–408 ppm), low contents of Yb (0.32–1.00 ppm) and Y (3.41–10.3 ppm) with high Sr/Y ratios (21.77–96.77) and depletion in HFSE Nb, Ta and Ti. These characteristics are similar to those of the high-Si adakitic rocks. The melanocratic dioritic gneiss has low SiO2 (59.81%), high MgO (6.34%), high Al2O3 (14.02%) contents, rich in Na2O (3.7%) and poor in K2O (1.79%), with high Mg index (Mg# = 67). REE and trace elements are on the whole similar to that of the tonalitic gneiss, but compatible element abundances V (116 ppm), Cr (249 ppm), Co (37 ppm) and Ni (179 ppm) are higher. The leucocratic felsic bands (approximating trondhjemite in composition) have major oxides similar to that of the TTG gneisses but the REE and compatible elements are extremely low, which are indicative of the products of anatexis. The tonalitic gneiss has positive εNd(t) (2.37–3.29) and low initial Sr (0.69719–0.70068) values with depleted mantle Nd model age of ca. 2.8 Ga, suggesting its generation from partial melting of mantle-derived juvenile crust. The dioritic gneiss was also derived from subduction environment, but has undergone significant metasomatism of mantle wedge. The delineation of the ca. 2.7 Ga TTG gneisses in the Zanhuang Complex further proves that the North China Craton experienced large-scale continental crustal accretion in early Neoarchean, and gives new constraints on the subdivision of the early blocks and greenstone belts of the craton.  相似文献   

17.
The newly discovered Fuxing porphyry Cu deposit is located in the Dananhu–Tousuquan arc, adjacent to the Tuwu–Yandong Cu deposits of Eastern Tianshan, in the southern Central Asian Orogenic Belt. The Fuxing deposit is hosted by volcanic rocks (basalt and dacite) in the Early Carboniferous Qi'eshan Group and Carboniferous felsic intrusions (plagiogranite porphyry, monzogranite, and quartz diorite). New SIMS zircon U–Pb dating indicates that the plagiogranite porphyry and monzogranite emplaced at 332.1 ± 2.2 Ma and 328.4 ± 3.4 Ma, respectively. The basalts are characterized by low SiO2 contents (47.47–54.90 wt.%), a lack of Eu anomalies, strong depletion of Na, Ta, and Ti elements but positive Sr, U, and Pb anomalies, high Y (20.8–28.2 ppm) and HREE concentrations (Yb = 2.23–3.06 ppm), and relatively low (La/Yb)N (2.20–3.92) values; the dacite samples have high SiO2 contents (66.13–76.93 wt.%), clearly negative Eu anomalies, high Mg# values (36–51), and high Y (41.8–54.9 ppm) and Yb (5.76–8.98 ppm) concentrations. The basalts and dacites exhibit similar signatures as normal arc rocks, and were considered to be derived from partial melting of mantle-wedge peridotite that was previously metasomatized by slab melts. In contrast, the plagiogranite porphyry, monzogranite, and quartz diorite show the same geochemical affinity with modern adakites, which are characterized by high SiO2 contents (67.55–79.00 wt.%), minor negative to positive Eu anomalies, strong depletion of heavy rare earth elements (Yb = 0.17–1.19 ppm) and Y (1.86–10.1 ppm), positive K, Rb, Sr, and Ba but negative Nb, Ta, Th, and Ti anomalies, and high (La/Yb)N ratios and Mg# values. Moreover, these adakitic felsic intrusions display relatively high positive zircon εHf(t) values (+ 11.4 to + 18.3), low 87Sr/86Sr (0.706080–0.711239), high 143Nd/144Nd (0.512692–0.512922) ratios, and consistent zircon δ18O values (4.41‰–5.48‰), suggesting that their parental magma were most likely derived from partial melting of the subducted oceanic crust followed by mantle peridotite interaction. Based on the whole-rock geochemical and Sr–Nd–Hf–O isotopic data, as well as detailed petrographic analyses, we further suggest that the Fuxing igneous rocks and associated porphyry Cu mineralization were generated by the northward subduction of the paleo-Tianshan oceanic plate beneath the Dananhu–Tousuquan island arc during the Early Carboniferous.  相似文献   

18.
Carbonate cements in late Dinantian (Asbian and Brigantian) limestones of the Derbyshire carbonate platform record a diagenetic history starting with early vadose meteoric cementation and finishing with burial and localized mineral and oil emplacement. The sequence is documented using cement petrography, cathodoluminescence, trace element geochemistry and C and O isotopes. The earliest cements (Pre-Zone 1) are locally developed non-luminescent brown sparry calcite below intrastratal palaeokarsts and calcretes. They contain negligible Fe, Mn and Sr but up to 1000 ppm Mg. Their isotopic compositions centre around δ18O =?8.5‰, δ13C=?5.0‰. Calcretes contain less 13C. Subsequent cements are widespread as inclusion-free, low-Mg, low-Fe crinoid overgrowths and are described as having a‘dead-bright-dull’cathodoluminescence. The‘dead’cements (Zone 1) are mostly non-luminescent but contain dissolution hiatuses overlain by finely detailed bright subzones that correlate over several kilometres. Across‘dead'/bright subzones there is a clear trend in Mg (500–900 ppm), Mn (100–450 ppm) and Fe (80-230 ppm). Zone 1 cements have isotopic compositions centred around δ18O =?8.0‰ and δ13C=?2.5‰. Zone 2 cement is bright, thin and complexly subzoned. It is geochemically similar to bright subzones of Zone 1 cements. Dull Zone 3 cement pre-dates pressure dissolution and fills 70% or more of the pore space. It generally contains little Mn, Fe and Sr but can have more than 1000 ppm Mg, increasing stratigraphically upwards. The δ18O compositions range from ?5.5 to ?15‰ and the δ13C range is ?1 to + 3.20/00. Zone 4 fills veins and stylolite seams in addition to pores. It is synchronous with Pb, Ba, F ore mineralization and oil migration. Zone 4 is ferroan with around 500 ppm Fe, up to 2500 ppm Mg and up to 1500 ppm Mn. Isotopic compositions range widely; δ15O =?2.7 to ?9‰ and δ13C=?3.8 to+2.50‰. Unaltered marine brachiopods suggest a Dinantian seawater composition around δ15O = 0‰ (SMOW), but vital isotopic effects probably mask the original δ13C (PDB) value. Pre-Zone 1 calcites are meteoric vadose cements with light soil-derived δ13C and light meteoric δ18O. An unusually fractionated‘pluvial’δ15O(SMOW) value of around — 6‰ is indicated for local Dinantian meteoric water. Calcrete δ18O values are heavier through evaporation. Zone 1 textures and geochemistry indicate a meteoric phreatic environment. Fe and Mn trends in the bright subzones indicate stagnation, and precipitation occurred in increments from widespread cyclically developed shallow meteoric water bodies. Meteoric alteration of the rock body was pervasive by the end of Zone 1 with a general resetting of isotopic values. Zone 3 is volumetrically important and external sources of water and carbonate are required. Emplacement was during the Namurian-early Westphalian by meteoric water sourced at a karst landscape on the uplifted eastern edge of the Derbyshire-East Midland shelf. The light δ18O values mainly reflect burial temperatures and an unusually high local heat flow, but an input of highly fractionated hinterland-derived meteoric water at the unconformity is also likely. Relatively heavy δ13C values reflect the less-altered state of the source carbonate and aquifer. Zone 4 is partly vein fed and spans burial down to 2000 m and the onset of tectonism. Light organic-matter-derived δ13C and heavy δ18O values suggest basin-derived formation water. Combined with textural evidence of geopressures, this relates to local high-temperature ore mineralization and oil migration. Low water-to-rock ratios with host-rock buffering probably affected the final isotopic compositions of Zone 4, masking extremes both of temperature and organic-matter-derived CO2.  相似文献   

19.
This study provides 87Sr/86Sr, δ13C and δ18O data from the best-preserved limestone and dolomite of the Ediacaran carbonate-dominated Khorbusuonka Group of the Olenek Uplift, NE Siberian Craton, as well as detrital zircon geochronological data from both underlying and overlying sandstones. The Maastakh Formation is characterized by 87Sr/86Sr ratios of ca. 0.70822 and δ13C values between + 4.8 and + 6.0‰. 87Sr/86Sr ratios in limestones of the Khatyspyt Formation are fairly uniform, ranging from 0.70783 to 0.70806. The carbon isotopic composition slowly decreases from bottom (+ 3.7‰) to top (− 0.2‰) of section. The Sr isotopic composition of the Turkut Formation varies from 0.70824 to 0.70914, value of δ13C is about zero: − 0.7…+0.7 ‰. The youngest population of detrital zircons from Maastakh Formation indicates that these rocks were formed not later than 630 Ma. U–Pb detrital zircons data of Kessyusa Group has a single peak at about 543 Ma, which is almost identical to the earlier dating. Based on biostratigraphy and isotopic data, the Sr isotopic compositions from the Khatyspyt Formation (87Sr/86Sr = 0.70783–0.70806) represent the composition of seawater at 560–550 Ma. Such low values of 87Sr/86Sr ratio in Ediacaran water were probably caused by the quick opening of Iapetus Ocean.  相似文献   

20.
It is generally accepted that the low-Mg adakitic rocks were derived from the partial melting of metabasalts/eclogites. In this study, we demonstrate that the early Cretaceous low-Mg adakitic granites in the North Dabie Complex (NDC) were generated by the partial melting of the NDC orthogneisses. Here we present in-situ U–Pb and Lu–Hf isotopes in zircon with whole-rock geochemical and Sr–Nd isotopic compositions were carried out for the Tiantangzhai porphyritic monzogranites from the Dabie orogen, eastern China. The monzogranites are characterized by high Sr (576–988 ppm), low Y (7.3–19.0 ppm), and depletion in HREE (Yb: 0.50–1.78 ppm) (thus resulting in high Sr/Y (34.3–135.2) and (La/Yb)N (17.0–105.2) ratios) without a negative Eu anomaly. They also exhibit high SiO2 (66.5–73.5 wt.%) and K2O (2.7–4.7 wt.%), and low MgO (0.4–1.6 wt.%) or Mg# (28.2–45.3, mostly < 40) values. Whole-rock geochemical compositions suggest that the monzogranites represent low-Mg adakitic rock with high-Si and rich-K features equilibrated with residues rich in garnet. Sr–Nd isotopic compositions (εNd (t) = ? 16.2 to ? 20.3, (87Sr/86Sr)i = 0.707798–0.708804, tDM2(Nd) = 2.3–2.6 Ga) of the monzogranites are distinct from that of the eclogites and amphibolites in the Dabie orogen, but similar to that of the Neoproterozoic (700–800 Ma) gneisses in the NDC. U–Pb dating of zircons gives a consistent age of 130.0 ± 3.4 Ma with discordia upper intercept age of 716 ± 34 Ma for inherited cores identified by CL imaging. Correspondingly, in-situ Lu–Hf analyses of early Cretaceous young age-spots from zircons yield initial 176Hf/177Hf ratios from 0.281898 to 0.282361, εHf(t) values from ? 28.1 to ? 17.6 and two-stage “crust” Hf model ages (tDM2) from 2293 ± 89 to 2949 ± 108 Ma, which are generally in agreement with values of 0.281891 to 0.282218, ? 28.2 to ? 11.7 and 1927 ± 87 to 2963 ± 92 Ma for the pre-Mesozoic inherited cores, respectively. As for individual core-rim pairs in zircon, Th/U ratios increase from the inherited cores to the young growth rims possibly due to variable degrees of partial melting, whereas 176Lu/177Hf ratios greatly decrease because of the garnet effect in residues. Thus, we suggest that the early Cretaceous low-Mg adakitic granites were derived from the partial melting of the NDC Neoproterozoic (700–800 Ma) gneisses, and the foundering of the garnet-bearing residues could have caused the destruction of the over-thickened lower continental crust.  相似文献   

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