安徽庐枞盆地罗河铁矿床中榍石LA-ICP-MS U-Pb定年及其意义

罗河铁矿床位于长江中下游铁铜金成矿带庐枞矿集区,已探明资源量约10亿吨,是成矿带内最大的铁矿床。矿床主成矿阶段广泛发育热液成因榍石,以榍石-硬石膏-磷灰石组合为特征,在矿床-800~-900m和-1500~-1600m两个不同深度稳定发育,为确定成矿时代和成矿流体演化提供了良好的研究对象。本次工作对罗河铁矿床深部和浅部两层矿体中热液榍石开展了年代学及地球化学研究,结果表明榍石中存在(Al,Fe)~(3+)+(F,OH)~-=Ti~(4+)+O~(2-)置换反应,并富含Zr、Nb和REE等元素。榍石中Zr含量估算矿床成矿温度约700℃,指示玢岩型矿床比矽卡岩型铁矿床具有更高的成矿温度,高温条件有利于Ti元素的迁移。榍石的稀土元素配分图均呈现出明显右倾,并具较高的稀土元素总量以及明显的负Eu异常特征,轻稀土富集表明其结晶早于磷灰石和绿帘石等矿物,形成于高温热液环境,不同深度榍石的Eu异常变化表明成矿流体的氧逸度从深部到浅部有所升高。热液榍石原位微区LA-ICPMS U-Pb定年结果表明,上、下两层榍石形成时代分别为130.0±0.9Ma和129.1±0.8Ma~129.7±0.8Ma,表明罗河铁矿床两层矿体是同一成矿系统的在不同深度的产物。矿床成矿时代与区内隐伏闪长岩体成岩时代一致,结合矿床地质特征研究,本文认为闪长玢岩是矿床的成矿母岩。罗河铁矿床属于燕山晚期岩浆热液活动的产物,形成于区域早白垩世岩石圈减薄的环境。     

Lu–Hf constraints on pre-, syn,and post-collision associations of the Gurupi Belt,Brazil: Insights on the Rhyacian crustal evolution

The Gurupi Belt (together with the São Luís cratonic fragment), in north-northeastern Brazil, has been described in previous studies that used extensive field geology, structural analysis, airborne geophysics, zircon U–Pb dating, and whole-rock Sm–Nd isotope and geochemical data as a polyphase orogenic belt, with the Rhyacian being the main period of crust formation. This was related to a 2240 Ma to 2140 Ma accretionary processes that produced juvenile crust, which has subsequently been reworked during a collisional event at 2100 ± 20 Ma, with little evidence of Archean crust. In this study, we use Lu–Hf isotopic data in zircon from granitoids (including gneiss) of variable magmatic series, and amphibolite to improve the knowledge of this scenario, and investigate additional evidence of recycling of Archean basement. Pre-collisional high Ba-Sr and ferroan granitoids and amphibolite formed in island arc (2180–2145 Ma), show only zircons with suprachondritic εHf values (ca. +1 to +8) indicating the large predominance of juvenile magmas. Only 10% of the data show slightly negative εHf values (0 to ?4), which have been observed in granodiorite-gneiss formed in continental arc (2170–2140 Ma), and in strongly peraluminous collisional granites (2125–2070 Ma), indicating the rework of older Paleoproterozoic to Archean components (Hf_TDM = 2.11–3.69 Ga). A two-component mixing model using both Hf and published Nd isotope data are in line with this interpretation and indicate more than 90% of juvenile material, and less influence of Archean materials. Comparing with other Rhyacian terranes that are interpreted to have been close to Gurupi in a pre-Columbia configuration (ca. 2.0 Ga), our results differ from those of SE-Guiana Shield, which show strong influence of Archean protoliths, and are very similar to those of the central-eastern portion of the Baoulé-Mossi Domain of the West African Craton, which has also been formed largely by juvenile magmas in an accretionary-collisional orogen.     

Geochemical Constraints on the Origin of Volcanic Rocks from the Andean Northern Volcanic Zone, Ecuador

Whole-rock geochemical data on basaltic to rhyolitic samplesfrom 12 volcanic centers are used to constrain the role of continentalcrust in the genesis of magmas formed beneath the anomalouslywide subduction-related volcanic arc in Ecuador. Relativelyhomogeneous, mantle-like, isotopic compositions across the arcimply that the parental magmas in Ecuador were produced largelywithin the mantle wedge above the subduction zone and not byextensive melting of crustal rocks similar to those upon whichthe volcanoes were built. Cross-arc changes in ¹⁴³Nd/¹⁴⁴Nd and7/4Pb are interpreted to result from assimilation of geochemicallymature continental crust, especially in the main arc area, 330–360km from the trench. Mixing calculations limit the quantity ofassimilated crust to less than 10%. Most andesites and dacitesin Ecuador have adakite-like trace element characteristics (e.g.Y <18 ppm, Yb <2 ppm, La/Yb >20, Sr/Y >40). Availablewhole-rock data do not provide a clear basis for distinguishingbetween slab-melting and deep crustal fractionation models forthe genesis of Ecuador adakites; published data highlightinggeochemical evolution within individual volcanoes, and in magmaticrocks produced throughout Ecuador since the Eocene, appear tosupport the deep fractionation model for the genesis of mostevolved Ecuadoran lavas. A subset of andesites, which displaya combination of high Sr (>900 ppm), Nd >4·1 and7/4Pb <6·0, appear to be the best candidates amongEcuador lavas for slab-melts associated with the subductionof the relatively young, over-thickened, oceanic crust of theCarnegie Ridge. KEY WORDS: andesite; Ecuador; trace elements; isotopes; adakite     

Quantification of karst aquifer discharge components during storm events through end-member mixing analysis using natural chemistry and stable isotopes as tracers

Karst aquifer components that contribute to the discharge of a water supply well in the Classical Karst (Kras) region (Italy/Slovenia) were quantitatively estimated during storm events. Results show that water released from storage within the epikarst may comprise as much as two-thirds of conduit flow in a karst aquifer following rainfall. Principal components analysis (PCA) and end-member mixing analysis (EMMA) were performed using major ion chemistry and the stable isotopes of water (δ¹⁸O, δ²H) and of dissolved inorganic carbon (δ¹³C_DIC) to estimate mixing proportions among three sources: (1) allogenic river recharge, (2) autogenic recharge, and (3) an anthropogenic component stored within the epikarst. The sinking river most influences the chemical composition of the water-supply well under low-flow conditions; however, this proportion changes rapidly during recharge events. Autogenic recharge water, released from shallow storage in the epikarst, displaces the river water and is observed at the well within hours after the onset of precipitation. The autogenic recharge end member is the second largest component of the well chemistry, and its contribution increases with higher flow. An anthropogenic component derived from epikarstic storage also impacts the well under conditions of elevated hydraulic head, accounting for the majority of the chemical response at the well during the wettest conditions.     

海拉尔盆地西部蚀源区岩石提供铀源能力的研究

利用U-Pb同位素组成演化对海拉尔盆地西部西胡里吐盆地蚀源区火山岩类和克鲁伦凹陷蚀源区花岗岩类岩石的研究表明:蚀源区岩石原始铀含量(U0)较高,火山岩类平均U0为10.061×106,铀变化系数(ΔU)平均为49.57%;花岗岩类平均U0为18.381×106,ΔU平均为80%。这些结果显示了蚀源区岩石能为沉积砂体提供预富集的物质基础,也能提供成矿铀源。岩石的U-Ra平衡系数研究表明,火山岩类存在明显的U-Ra不平衡现象,而花岗岩提供成矿铀源应发生在16000a以前。     

Carbon and oxygen isotopic constraints on paleoclimate and paleoelevation of the southwestern Qaidam basin,northern Tibetan Plateau

We investigate the growth of the northern Tibetan Plateau and associated climate change by applying oxygen and carbon isotopic compositions in Cenozoic strata in the southwestern Qaidam basin. The X-ray diffraction and isotopic studies reveal that the carbonate minerals are mainly authigenic and they do not preserve any evidence for detrital carbonate and diagenesis. The isotope data show large fluctuations in the δ¹⁸O and δ¹³C values in the middle–late Eocene, indicating relatively warm and seasonal dry climate. The positive correlation of the δ¹⁸O and δ¹³C values in the Oligocene and the positive shift of the δ¹³C values from the Eocene to Oligocene suggest that the climate changed to arid in the Oligocene. However, the δ¹⁸O values show negative shift, which is closely related to the global cooling event. During the Miocene, the δ¹³C values vary between –2‰ and –4‰, whereas the δ¹⁸O values show continuous negative shift. The mean δ¹⁸O values decrease from –8.5‰ in the early Miocene to –10.0‰ in the late Miocene. The stable isotope-based paleoaltimetry results suggest that the elevation of the southwestern Qaidam basin was approximately 1500 m in the middle–late Eocene and Oligocene. Subsequently, during Miocene the crustal uplift process started and the elevation reached approximately 2000 m in the early Miocene and 2500 m in the late Miocene, which suggests large-scale growth of the northern Tibet Plateau during the Miocene.     

Paleoceanographic evolution of the SW Svalbard margin (76°N) since 20,000 C yr BP

Two cores from the southwestern shelf and slope of Storfjorden, Svalbard, taken at 389 m and 1485 m water depth have been analyzed for benthic and planktic foraminifera, oxygen isotopes, and ice-rafted debris. The results show that over the last 20,000 yr, Atlantic water has been continuously present on the southwestern Svalbard shelf. However, from 15,000 to 10,000 ¹⁴C yr BP, comprising the Heinrich event H1 interval, the Bølling-Allerød interstades and the Younger Dryas stade, it flowed as a subsurface water mass below a layer of polar surface water. In the benthic environment, the shift to interglacial conditions occurred at 10,000 ¹⁴C yr BP. Due to the presence of a thin upper layer of polar water, surface conditions remained cold until ca. 9000 ¹⁴C yr BP, when the warm Atlantic water finally appeared at the surface. Neither extensive sea ice cover nor large inputs of meltwater stopped the inflow of Atlantic water. Its warm core was merely submerged below the cold polar surface water.     

<Superscript>57</Superscript>Fe Mössbauer measurements and electronic structure calculations on natural lawsonites

Three natural lawsonites from Syke Rock, Mendocino Co., Reed Ranch, Marin Co., and Blake Gardens, Sonoma Co., all from the Coast Range Region in California, were studied by ⁵⁷Fe Mössbauer spectroscopy, electron microprobe analysis, and X-ray powder diffraction. The samples contain about 0.6, 1.0, and 1.4 wt% of total iron oxide, respectively. ⁵⁷Fe Mössbauer spectra are consistent with the assumption that high-spin Fe³⁺ substitutes for Al in the octahedrally coordinated site. The Mössbauer spectrum of lawsonite from Syke Rock exhibits a second doublet with ⁵⁷Fe hyperfine parameters typical for octahedrally coordinated high-spin Fe²⁺. Electronic structure calculations in the local spin density approximation yield quadrupole splittings for Fe³⁺ in quantitative agreement with experiment indicating, however, that substitution of Al by Fe³⁺ must be accompanied by local distortion around the octahedral site. Model calculations also reproduce the room temperature hyperfine parameters of ferrous high-spin iron assuming the substitution of Ca by Fe²⁺. However, it cannot be excluded that Fe²⁺ may occupy a more asymmetric site within the microstructural cavity occupied by Ca and a H₂O molecule.     

∼3,850 Ma tonalites in the Nuuk region,Greenland: geochemistry and their reworking within an Eoarchaean gneiss complex

The Eoarchaean (>3,600 Ma) Itsaq Gneiss Complex of southern West Greenland is dominated by polyphase orthogneisses with a complex Archaean tectonothermal history. Some of the orthogneisses have c. 3,850 Ma zircons, and they vary from rare single phase metatonalites to more common complexly banded migmatites. This is due to heterogeneous strain, in situ anatexis and granitic veining superimposed during younger tectonothermal events. In the single-phase tonalites with c. 3,850 Ma zircon, oscillatory-zoned prismatic zircon is all 3,850 Ma old, but shows patchy ancient loss of radiogenic Pb. SHRIMP spot analyses and laser ablation ICP-MS depth profiling show that thin (usually < 10 μm) younger (3,660–3,590 Ma and Neoarchaean) shells of lower Th/U metamorphic zircon are present on these 3,850 Ma zircons. Several samples with this simple zircon population occur on islands near Akilia. In contrast, migmatites usually contain more complex zircon populations, with often more than one generation of igneous zircon present. Additional zircon dating of banded gneisses across the Complex shows that samples with c. 3,850 Ma igneous zircon are not just a phenomenon restricted to Akilia and adjacent islands. For example, migmatites from Itilleq (c. 65 km from Akilia) contain variable amounts of oscillatory-zoned 3,850 Ma and 3,650 Ma zircon, interpreted, respectively, as the rock age and the time of crustal melting under Eoarchaean metamorphism. With only 110–140 ppm Zr in the tonalites and likely magmatic temperatures of >850°C, zircon solubility–melt composition relationships show that they were only one-third saturated in zircon. Any zircon entrained in the precursor magmas would thus have been highly soluble. Combined with the cathodoluminesence imaging, this demonstrates that the c. 3,850 Ma oscillatory zoned zircon crystallised out of the melt and hence gives a magmatic age. Thus the rare well-preserved tonalites and palaeosome in migmatites testify that c. 3,850 Ma quartzo–feldspathic rocks are a widespread (but probably minor) component in the Itsaq Gneiss Complex. C. 3,850 Ma zircon with negative Eu anomalies (showing growth in felsic systems) also occurs as detrital grains in rare c. 3,800 Ma metaquartzites and as inherited grains in some 3,660 Ma granites (sensu stricto). These demonstrate that still more c. 3,850 Ma rocks were present, but were recycled into Eoarchaean sediments and crustally derived granites. The major and trace element characteristics (e.g. LREE enrichment, HREE depletion, low MgO) of the best-preserved c. 3,850 Ma rocks are typical of Archaean TTG suites, and thus argue for crust formation processes involving important contributions from melting of hydrated mafic crust to the earliest Archaean. Five c. 3,850 Ma tonalites were selected as the best preserved on the basis of field criteria and zircon petrology. Four of these samples have overlapping initial ɛ_Nd (3,850 Ma) values from +2.9 to +3.6± 0.5, with the fourth having a slightly lower value of +0.6. These data provide additional evidence for a markedly LREE-depleted early terrestrial mantle reservoir. The role of c. 3,850 Ma crust should be considered in interpreting isotope signatures of the younger (3,800–3,600 Ma) rocks of the Itsaq Gneiss Complex. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Hydrogeology of the Winnipeg Formation in Manitoba, Canada

The Winnipeg Formation is the basal sedimentary unit throughout much of southern and central Manitoba, Canada, where it forms a regional aquifer over most of its extent. This aquifer is an important source of water in southeastern Manitoba and in Manitoba’s Interlake area, but in most other areas, groundwater within the aquifer is saline. Chemical and isotopic evidence indicate the presence of groundwaters of three different origins: (1) basin brines; (2) modern meteoric recharge; and (3) subglacial recharge that occurred during the late Pleistocene. Hydraulic head and sedimentary facies distributions indicate that the flow system in parts of the area is not in a state of equilibrium and saline waters will encroach on areas currently occupied by freshwater in some areas, while in other areas, freshwater will replace saline water. These features must be considered in groundwater resource management, as groundwater withdrawals will likely hasten these processes.

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Resumen La Formación Winnipeg es la unidad sedimentaria basal en la mayor parte de Manitoba central, Canadá, donde forma un acuífero regional en la mayor parte de su extensión. Este acuífero es una fuente importante de agua en el Sureste de Manitoba y el área de entrelagos de Manitoba, pero en la mayoría de las otras zonas del acuífero, el agua es salina. Las evidencias químicas e isotópicas indican que existen aguas subterráneas de tres orígenes diferentes: (1) salmueras de cuenca; (2) recarga meteórica actual; y (3) recarga subglacial ocurrida durante el Pleistoceno Superior. Los niveles piezométricos y la distribución de las facies sedimentarias indican que el sistema de flujo no se encuentra en estado de equilibrio en parte del área y las aguas salinas irán invadiendo áreas actualmente ocupadas con aguas dulces, mientras que en otras zonas el agua dulce está reemplazando al agua salina. Estos hechos deben ser considerados en la gestión de las aguas subterráneas como recurso, ya que las extracciones de agua acelerarán probablemente estos procesos.

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Résumé La Formation de Winnipeg est l’unité sédimentaire de base sur la plus grande partie du Sud et du centre du Manitoba au Canada, où elle forme un aquifère régional sur pratiquement toute son extension. Cet aquifère représente une ressource en eau importante dans le Sud-Est du Manitoba et dans les zones d’entre les lacs, mais salée dans la plus part des autres zones. Les indications isotopiques et chimiques permettent de distinguer trois différentes origines des eaux souterraines: (1) les saumures de bassin; (2) la recharge météoritique moderne; (3) la recharge sub-glaciaire qui est apparue durant le Pléistocène récent. Les charges hydrauliques et la distribution des faciès sédimentaires indiquent que le système d’écoulement dans certaines zones n’est pas dans un état d’équilibre et que les eaux salées empièteront sur des zones d’eau douce, tandis que dans d’autres zones l’eau douce remplacera les eaux salées. Ces aspects doivent être considérés dans la gestion des ressources en eau souterraine, car le prélèvement des eaux souterraines pourrait accentuer ces processus.