Lead isotopic composition and genesis of Phanerozoic metal deposits in China

Lead isotopic compositions of more than 130 galena specimens from Phanerozoic metal deposits in China have been analyzed with a standard deviation of less than 0.5%. The ranges of isotopic composition are from 17.8 to 19.3 for Pb²⁰⁶/Pb²⁰⁴, 15.2 to 16.0 for Pb²⁰⁷/Pb²⁰⁴ and 37 to 40.8 for Pb²⁰⁸/Pb²⁰⁴. These values overlap those of MORB, pelagic chemical sediments and intra-oceanic arcs of western Pacific in plots of Pb²⁰⁷/Pb²⁰⁴ vs. Pb²⁰⁶/Pb²⁰⁴ and Pb²⁰⁸/Pb²⁰⁴ vs. Pb²⁰⁶/Pb²⁰⁴. This indicates that mixing between mantle and crustal materials due to partial melting of the Pacific subduction slab is the principal mechanism for ore genesis. On the basis of global Precambrian conformable leads, together with that of Guanmenshan, Pengjiapu and Baiyun deposits in China, it is suggested that mantle lead was developed in a single stage with a (U²³⁸/Pb²⁰⁴) value of 7.8. If the ages of igneous rocks associated with these deposits are adopted as formation ages, the mean Th/U of the second stage of crust-mantle evolution can be calculated with a lead mixing model. The meanμ value of China continent is 9.98±0.78, which is in agreement with that of global conformable leads, 9.81±0.58. The mean Th/U ratio of 4.27 is distinctly larger than the global value (3.81), indicating that the China continent is rich in Th. Simultaneously, mean formation ages have also been obtained of the continental crusts in various regions, ranging from 3,000 to 3,800 m.y. and from 2,500 to 2,700 m.y., which are comparable with the age distribution of global Archaean cratons.     

Makran ophiolitic basalts (SE Iran) record Late Cretaceous Neotethys plume-ridge interaction

ABSTRACT

The Makran complex in southeast Iran provides a spectacular subduction-related accretionary complex to understand the mechanism of oceanic accretion and the evolution of subduction zones. In this paper, we present new major and trace element data as well as isotopic compositions of mafic volcanic blocks from the Makran ophiolitic mélange complex (OMC). Our aim is to assess the genesis of these rocks and discuss their implications on the evolution of Neotethys Ocean. These volcanic blocks are composed mainly of basalts with minor trachytes. The Makran lavas are occasionally interlayered with tuff layers. Zircons from these tuffs give U-Pb ages of 95 Ma, which is well in accordance with the reposted microfossil data for the interlayered pelagic limestones with pillow lavas. Makran basalts can be geochemically subdivided into four groups; normal to transitional MORB, enriched-MORB, Plume-type MORB and alkaline (-OIB-like) basalts. The OIB-like pillow lavas are represented by high values of Th/Tb (6.3–7.4) which are higher than other basalts (group 1 = 0.3–0.8; groups 2 = 0.7–1.6; group 3 = 1.58–1.36).¹⁴³Nd/¹⁴⁴Nd_(t) ratios for basalts ranges from 0.51247 to 0.51292, whereas ⁸⁷Sr/⁸⁶Sr_(t) isotopic composition of the OMC lavas varies from 0.704433 to 0.709466. The Pb isotopic composition of the lavas are quite high, ranging from 15.49–15.66 for ²⁰⁷Pb/²⁰⁴Pb_(t), 18.09–19.12 for ²⁰⁶Pb/²⁰⁴Pb_(t) and 37.80–39.23 for ²⁰⁸Pb/²⁰⁴Pb_(t). The chemistry of these rocks suggests that they were formed most likely in an oceanic setting with clear plume-ridge interaction. These rocks can form from partial melting of a highly heterogeneous mantle source, which is extensively metasomatized with deep mantle OIB-type components. We suggest these rocks have been generated in an oceanic ridge with plume-ridge interaction, similar to the Iceland-Reykjanes Ridge, before being fragmented and accreted into the Makran accretionary complex.     

Sulphur and Lead Isotope Compositions of the Dajiangp—ing Deposit in Western Guangdong Province1

Abstract The Dajiangping pyrite deposit located in the middle sector of the Yunkai uplift in western Guangdong is a stratiform sulphide deposit occurring in Sinian marine clastic and fine clastic rocks. The formation of the deposit was related to submarine exhalation and hot brine deposition. A part of it was reformed by late-stage hydro thermal solution. The δ³⁴S values of pyrite vary from — 25.55‰ to + 21.07‰, which are inversely proportional to the content of organic carbon in ore and pyrite. Passing from striped fine-grained pyrite ore to massive coarse-grained pyrite ore, i.e. from south to north, the sulphur isotopic composition changes from the light sulphur-enriched one to the heavy sulphur-enriched one. The lead isotopic composition of striped ore is consistent with that of the country locks of orebodies and the lead is radiogenic lead derived from the upper crust. The lead isotopic composition of massive ore is relatively homogeneous and its ²⁰⁶/Pb²⁰⁴Pb, ²⁰⁷/Pb²⁰⁴Pb and ²⁰⁸/Pb²⁰⁴Pb ratios are a bit lower than those of striped ore; the lead result from mixing of synsedimentary ore lead with that derived from basement migmatite brought by late-stage hydrothermal solutions.     

Lead isotopes of the carbonate-hosted Kabwe, Tsumeb, and Kipushi Pb-Zn-Cu sulphide deposits in relation to Pan African orogenesis in the Damaran-Lufilian Fold Belt of Central Africa

Lead isotope ratios of galena from the carbonate-hosted massive sulphide deposits of Kabwe (Pb-Zn) and Tsumeb (Pb-Zn-Cu) in Zambia and Namibia, respectively, have been measured and found to be homogeneous and characteristic of upper crustal source rocks. Kabwe galena has average isotope ratios of ^206/204Pb = 17.997 ± 0.007, ^207/204Pb = 15.713 ± 0.010 and ^208/204Pb = 38.410 ± 0.033. Tsumeb galena has slightly higher ^206/204Pb (18.112 ± 0.035) and slightly lower ^207/204Pb (15.674 ± 0.016) and ^208/204Pb (38.276 ± 0.073) ratios than Kabwe galena. The isotopic differences are attributed to local differences in the age and composition of the respective source rocks for Kabwe and Tsumeb. The homogeneity of the ore lead in the two epigenetic deposits suggests lead sources of uniform isotopic composition or, alternatively, thorough mixing of lead derived from sources with relatively similar isotopic compositions. Both deposits have relatively high ²³⁸U/²⁰⁴Pb ratios of 10.31 and 10.09 for Kabwe and Tsumeb galenas, respectively. These isotope ratios are considered to be typical of the upper continental crust in the Damaran-Lufilian orogenic belt, as also indicated by basement rocks and Cu-Co sulphides in stratiform Katangan metasediments which have a mean μ-value of 10.25 ± 0.12 in the Copperbelt region of Zambia and the Democratic Republic of Congo (formerly Zaire). The ²³²Th/²⁰⁴Pb isotope ratios of 43.08 and 40.42 for Kabwe and Tsumeb suggest Th-enriched source regions with ²³²Th/²³⁵U (κ-values) of 4.18 and 4.01, respectively. Model isotopic ages determined for the Kabwe (680 Ma) and Tsumeb (530 Ma) deposits indicate that the timing of the mineralisation was probably related to phases of orogenic activity associated with the Pan-African Lufilian and Damaran orogenies, respectively. Galena from the carbonate-hosted Kipushi Cu-Pb-Zn massive sulphide deposit in the Congo also has homogeneous lead isotope ratios, but its isotopic composition is comparable to that of the average global lead evolution curve for conformable massive sulphide deposits. The μ (9.84) and κ (3.69) values indicate a significant mantle component, and the isotopic age of the Kipushi deposit (456 Ma) suggests that the emplacement of the mineralisation was related to a post-tectonic phase of igneous activity in the Lufilian belt. The isotope ratios (^206/204Pb, ^207/204Pb, ^208/204Pb) of the three deposits are markedly different from the heterogeneous lead ratios of the Katangan Cu-Co stratiform mineralisation of the Copperbelt as well as those of the volcanogenic Nampundwe massive pyrite deposit in the Zambezi belt which typically define radiogenic linear trends on lead-lead plots. The host-rock dolomite of the Kabwe deposit also has homogeneous lead isotope ratios identical to the ore galena. This observation indicates contamination of the Kabwe Dolomite Formation with ore lead during mineralisation. Received: 8 September 1997 / Accepted: 21 August 1998     

Pb Isotopic Composition and Metal Sources of Au and Ag Deposits of the South Verkhoyansk Region (Yakutia,Russia) According to High-Precision MC-ICP-MS Data

The paper considers the results of high-precision Pb–Pb isotopic analysis of 120 galena samples from 27 Au and Ag deposits of the South Verkhoyansk Synclinorium (SVS) including large Nezhdaninsky deposit (628.8 t Au). The Pb isotopic composition is analyzed on a MC-ICP-MS NEPTUNE mass-spectrometer from solutions with an error of no more than ±0.02% (2σ). Four types of deposits are studied: (i) stratified vein gold–quartz deposits (type 1) hosted in metamorphosed Upper Carboniferous–Lower Permian terrigenous rocks and formed during accretion of the Okhotsk Block to the North Asian Craton synchronously with dislocation metamorphism and related granitic magmatism; (ii) vein gold–quartz (Nezhdaninsky type) deposits also hosted in Lower Permian metasedimentary rocks; (iii) Au–Bi deposits localized at the contact zones of the Late Cretaceous granitic plutons; and (iv) Sn–Ag polymetallic deposits related to granitic and subvolcanic rocks of the Okhotsk Zone of the SVS. The deposits of types 2, 3, and 4 are postaccretionary. The general range of ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios is 18.1516–18.5903 (2.4%), 15.5175–15.6155 (0.63%), and 38.3010–39.0481 (2.0%), respectively. In ²⁰⁶Pb/²⁰⁴Pb–²⁰⁷Pb/²⁰⁴Pb and ²⁰⁶Pb/²⁰⁴Pb–²⁰⁸Pb/²⁰⁴Pb diagrams, the data points of Pb isotopic compositions of all deposits occupy restricted, partly overlapping areas along a general elongated trend. The various SVS Au–Ag deposits can be classified according to the Pb isotopic composition in accordance with all three Pb ratios. Deposits of the same type show distinct Pb isotopic compositions that strongly exceed the scale of analytical error (±0.02%). The differences in Pb isotopic composition within specific deposits are low and subordinate and have little effect on variations in the Pb isotopic composition of the SVS deposits. The μ₂ values (Stacey–Kramers model), which characterize the ²³⁸U/²⁰⁴Pb ratios of ore lead sources of the SVS deposits, widely vary from 9.7 to 9.38. The ω₂ values (²³²Th/²⁰⁴Pb) are 39.82–36.61, whereas the Th/U ratios are 4.04–3.86. The content of all three radiogenic Pb isotopes and μ₂ values of feldspars from SVS intrusive rocks are strongly distinct from those of galena of stratified gold–quartz and vein gold–quartz deposits and are identical to Pb of galena from Au–Bi and Sn–Ag polymetallic deposits, indicating a mostly magmatic origin for the Pb of these deposits. Detailed isotopic study of the Nezhdaninsky deposit shows different Pb isotopic composition of two consecutive mineral assemblages (gold–sulfide and Ag polymetallic): ~0.30, ~0.07, and ~0.22% for ²⁰⁶Pb/²⁰⁴Pb, ²⁰⁷Pb/²⁰⁴Pb, and ²⁰⁸Pb/²⁰⁴Pb ratios, respectively. These differences are interpreted as a result of involvement of at least two metal sources during the evolution of an ore-forming system: (i) host Lower Permian terrigenous rocks and (ii) a magmatic source similar in Pb isotopic composition to that of Sn–Ag polymetallic deposits. The Pb isotopic composition and μ₂ and Th/U values show that lead of stratified gold–quartz deposits combines isotopic tracers of lower and upper crustal sources (Upper Carboniferous–Lower Permian terrigenous rocks), lead of which was mobilized by ore-bearing fluids. The high ²⁰⁸Pb/²⁰⁶Pb ratios and Th/U evolutionary parameter are common to all Pb isotopic composition of all studied Au–Ag deposits and SVS Cretaceous intrusive rocks and indicate that Pb sources were depleted in U relative to Th. Taking into account the structure of the region and conceptions on its evolution, we can suggest that the magma source was related to lower crustal subducted rocks of the Archean (~2.6 Ga) North Asian Craton and the Okhotsk terrane.     

Lead isotopic evidence for interaction between plume and lower crust during emplacement of peralkaline Lovozero rocks and related rare-metal deposits,East Fennoscandia,Kola Peninsula,Russia

The Lovozero alkaline massif—an agpaitic nepheline syenite layered intrusion—is located in the central part of the Kola Peninsula, Russia, and belongs to the Kola ultramafic alkaline and carbonatitic province (KACP) of Devonian age. Associated loparite and eudialyte deposits, which contain immense resources of REE, Nb, Ta, and Zr, constitute a world class mineral district. Previous Sr, Nd, and Hf isotope investigations demonstrated that these rocks and mineral deposits were derived from a depleted mantle source. However, because the Sr, Nd, and Hf abundances in the Kola alkaline rocks are significantly elevated, their isotopic compositions were relatively insensitive to contamination by the underlying crustal rocks through which the intruding magmas passed. Pb occurring in relatively lower abundance in the KACP rocks, by contrast, would have been a more sensitive indicator of an acquired crustal component. Here, we investigate the lead isotopic signature of representative types of Lovozero rocks in order to further characterize their sources. The measured Pb isotopic composition was corrected using the determined U and Th concentrations to the age of the crystallization of the intrusion (376?±?28 Ma, based on a ²⁰⁶Pb/²⁰⁴Pb versus ²³⁸U/²⁰⁴Pb isochron and 373?±?9 Ma, from a ²⁰⁸Pb/²⁰⁴Pb versus ²³²Th/²⁰⁴Pb isochron). Unlike the previously investigated Sr, Nd, and Hf isotopes, the lead isotopic composition plot was well outside the FOZO field. The ²⁰⁶Pb/²⁰⁴Pb values fall within the depleted MORB field, with some rocks having lower ²⁰⁷Pb/²⁰⁴Pb but higher ²⁰⁸Pb/²⁰⁴Pb values. Together with other related carbonatites having both lower and higher ²⁰⁶Pb/²⁰⁴Pb values, the combined KACP rocks form an extended linear array defining either a?~2.5-Ga secondary isochron or a mixing line. The projection of this isotopic array toward the very unradiogenic composition of underlying 2.4–2.5-Ga basaltic rocks of the Matachewan superplume and associated Archean granulite facies country rock provides strong evidence that this old lower crust was the contaminant responsible for the deviation of the Lovozero rocks from a presumed original FOZO lead isotopic composition. Evaluating the presence of such a lower crustal component in the Lovozero rock samples suggests a 5–10% contamination by such rocks. Contamination by upper crustal rock is limited to only a negligible amount.     

Geochronology and geochemistry of Cretaceous Nanshanping alkaline rocks from the Zijinshan district in Fujian Province,South China: Implications for crust–mantle interaction and lithospheric extension

In situ zircon U–Pb ages and Hf isotopic data, major and trace elements, and Sr–Nd–Pb isotopic compositions are reported for Nanshanping alkaline rocks from the Zijingshan district in southwestern Fujian Province (the Interior or Western Cathaysia Block) of South China. The Nanshanping alkaline rocks, which consist of porphyritic quartz monzonite, porphyritic syenite, and syenite, revealed a Late Cretaceous age of 100–93 Ma. All of the rocks show high SiO₂, K₂O + Na₂O, and LREE but low CaO, Fe₂O₃^T, MgO, and HFSE (Nb, Ta, P, and Ti) concentrations. These rocks also exhibit uniform initial ⁸⁷Sr/⁸⁶Sr ratios of 0.7078 to 0.7087 and ε_Nd(t) values of −4.1 to −7.2, thus falling within the compositional field of Cretaceous basalts and mafic dikes occurring in the Cathaysia Block. Additionally, these rocks display initial Pb isotopic compositions with a ²⁰⁶Pb/²⁰⁴Pb_i ratio of 18.25 to 18.45, a ²⁰⁷Pb/²⁰⁴Pb_i ratio of 15.63 to 15.67, and a ²⁰⁸Pb/²⁰⁴Pb_i ratio of 38.45 to 38.88. Combined with the zircon Hf isotopic compositions (ε_Hf(t) = −11.7 to −3.2), which are different from those of the basement rocks, we suggest that Nanshanping alkaline rocks were primarily derived from a subduction-related enriched mantle source. High Rb/Sr (0.29–0.65) and Zr/Hf (37.5–49.2) but relatively low Ba/Rb (4.4–8.1) ratios suggest that the parental magmas of these rocks were most likely formed via partial melting of a phlogopite-bearing mantle source with carbonate metasomatism. The relatively high SiO₂ (62.35–70.79 wt.%) and low Nb/Ta (10.0–15.3) ratios, positive correlation between SiO₂ and (⁸⁷Sr/⁸⁶Sr)_I, and negative correlation between SiO₂ and ε_Nd(t) of these rocks suggest that the crustal materials were also involved in formation of the Nanshanping alkaline rocks. Combined with geochemical and isotopic features, we infer magmatic processes similar to AFC (assimilation and fractional crystallization) involving early fractionation of clinopyroxene and olivine and subsequent fractionation of biotite-dominated assemblages coupled with a lesser amount of crustal contamination, thereby forming the Nanshanping alkaline rocks. The Nanshanping alkaline rocks appear to be associated with an extensional environment in the Cathaysia Block. This extensional regime could have resulted in the slab break-off and rollback of the subducting paleo-Pacific plate and the upwelling of the asthenospheric mantle, which induced partial melting of the enriched lithospheric mantle in the Cretaceous.     

Metal sources of the large Nezhdaninsky orogenic gold deposit, Yakutia, Russia: Results of high-precision MC-ICP-MS analysis of lead isotopic composition supplemented by data on strontium isotopes

A collection of galena from the Nezhdaninsky gold deposit (62 samples), as well as galena from the Menkeche silver-base-metal deposit and the Sentyabr occurrence and K-feldspar from intrusive rocks of the Tyry-Dyby ore cluster have been studied using the high-precision (±0.02%) MC-ICP-MS method. Particular ore zones are characterized by relatively narrow variations of isotope ratios (no wider than σ_6/4 = 0.26%). Vertical zoning of Pb isotopic composition is not detected. Variation in Pb isotope ratios mainly depends on the type of mineral assemblage. Galena of the gold-sulfide assemblage dominating at the Nezhdaninsky deposit is characterized by the following average isotope ratios: ²⁰⁶Pb/²⁰⁴Pb = 18.472, ²⁰⁷Pb/²⁰⁴Pb = 15.586, and ²⁰⁸Pb/²⁰⁴Pb = 38.605. Galena from the regenerated silver-base-metal assemblage is distinguished by less radiogenic lead isotope ratios: 18.420, 15.575, and 38.518, respectively. In lead from the Nezhdaninsky deposit, the component, whose source is identified as Permian host terrigenous rocks, is predominant. The data points of isotopic composition of lode lead make up a linear trend within the range of μ₂ = 9.5-9.6. K-feldspar of granitic rocks has less radiogenic and widely varying lead isotopic composition compared to that of galena. The isotopic data on Pb and Sr constrain the contribution of Late Cretaceous granitic rocks as a source of gold mineralization at the Nezhdaninsky deposit. The matter from the Early Cretaceous fluid-generating magma chamber participated in the ore-forming system of the Nezhdaninsky deposit. The existence of such a chamber is confirmed by the occurrence of Early Cretaceous granitoid intrusions on the flanks of the Nezhdaninsky ore field. The greatest contribution of magmatic lead (～30%) is noted in galena from the silver-base-metal mineral assemblage. This component has isotopic marks characteristic of lower crustal lead: the elevated ²⁰⁸Pb/²⁰⁶Pb ratio relative to the mean crustal value and the lower ²⁰⁷Pb/²⁰⁴Pb ratio. Taken together, they determine a high Th/U ～ 4.0 in the source and μ₂ = 9.37–9.50. This conclusion is consistent with the contemporary tectonic model describing evolution of the South Verkhoyansk sector of the Verkhoyansk Foldbelt and the Okhotsk Terrane.     

U-Th-Pb isotope systematics related to igneous rocks and ore Pb,Mount Isa,Queensland

This study is a search for a genetic relationship between Pb sulphide ore and igneous rocks in the region of Mount Isa, Queensland. The approach involves derivation of Pb isotope initial ratios by the whole-rock isochron method, and comparison of the initial ratios (Pb²⁰⁶/Pb²⁰⁴, Pb²⁰⁷/Pb²⁰⁴ and Pb²⁰⁸/Pb²⁰⁴) with the isotopic composition of the ore Pb. Data are reported for four igneous units; Kalkadoon granodiorite, Kalkadoon adamellite, Sybella granite and Eastern Creek volcanics. The results display considerable scatter for each of the units, and reveal the effects of recent surficial loss of U. The positioning of isochrons is aided by previous Rb-Sr geochronological data wherever possible. Comparison of initial ratios and ore Pb suggests that none of the igneous rock units is co-genetic with the ore deposit. Both phases of the Sybella Granite are more radiogenic and are apparently younger than the ore Pb. The Kalkadoon Granite is possibly related to the ore through some post-emplacement process of extraction and transport of Pb (e.g. by erosion or by anatectic magma generation) to the present site of the orebodies.     

Isotopic evolution of common lead

The isotopic composition of lead from galenas and feldspars of granitic rocks covering a time span of 3600 m.y. is reviewed. Hew data are combined with data from the literature, all ratios being normalized to a fixed value for the isotopic composition of lead in an inter-laboratory reference sample. Comparison of feldspar and galena results show that the isotopic composition of initial lead in granitic rocks may be identical to, or more radiogenic than, that in coeval stratiform (or ‘single stage’) ore deposits. The isotopic evolution of terrestrial lead over the past 3600 m.y. deduced from the stratiform ore data does not fit the closed system source. The data are best fitted to evolution models in which the value of μ (U²³⁸/Pb²⁰⁴ normalized to the present day) in the source has increased either over approximately the past 3.6 billion years or since the time of formation of the Earth. A limited number of high precision data for strontium likewise indicate open system isotopic evolution. In this system the Rb/Sr ratio appears to have decreased as a function of time. Physical models that explain the data are presented. Either mantle differentiation or crustal contamination processes could account for the change in μ in the source for the lead. The strontium data and some detailed studies of the isotopic composition of lead in oceanic volcanic rocks support mantle differentiation rather than crustal contamination. The exact nature of the mantle differentiation process cannot be specified, although empirical data favoring the existence of such a process are given. The best estimate of the age of the Earth, calculated with the data from 2750 and 3290 m.y.-old lead ores, is 4660 m.y.     

Sr and Pb isotopes,U and Th chemistry of the alkaline Monteregian and White Mountain igneous provinces,eastern North America

The Monteregian Hills and younger White Mountain alkaline intrusions were emplaced into the Cambro-Ordovician sediments of the St. Lawrence Lowlands and the folded and thrusted Lower Paleozoic sequence of the Appalachian orogen. Age relations indicate that there is a fine-scale structure to the igneous activity, with slightly undersaturated to critically saturated rocks emplaced between 141 and 128 Ma and strongly undersaturated rocks emplaced between 121 and 117 Ma.Sr and Pb isotopic data for the mantle-derived alkali picrite, alkali olivine basalt and basanite magmas, indicate derivation from a depleted mantle similar to that which produces present-day oceanic island basalts. For the most isotopically primitive samples, decay-corrected ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{= 0.7030–0.7037}$, ${}^{206}\text{Pb}{}^{204}\text{Pb}\text{= 19.05–19.72}$, ${}^{207}\text{Pb}{}^{204}\text{Pb}\text{= 15.56–15.65}$, and ${}^{208}\text{Pb}{}^{204}\text{Pb}\text{= 38.64–39.26}$. On Pb-Sr isotope correlation diagrams the data define trends similar to those for MOR basalts, implying mantle heterogeneity which requires the presence of a component enriched in radiogenic Pb relative to Sr. The interaction of these isotopically primitive magmas with the crust can be defined in terms of a three component system: depleted mantle-Grenville age crust-Lower Paleozoic age crust. The granitic magmas were apparently derived from the Lower Paleozoic crust of the Appalachian orogen.For the mantle-derived magmas, Th/U ratios vary from 2.5 (estimated ratio for MORB source) to 5.1, with the mean value near that of the bulk earth. The variations in Th/U suggest mantle heterogeneity on a local scale, and the high Th/U of some samples suggests that the mantle was enriched in incompatible elements shortly before melting. The magmas derived by partial melting of the crust have Th/U of 3.3 to 8.7, and the higher ratios are associated with rocks crystallized from magmas that originated by melting of Lower Paleozoic sediments.The Sr and Pb isotopic data support the conclusion of Bellet al. (1982) that the subcontinental mantle under eastern Canada underwent a Precambrian depletion event. This depleted mantle apparently extends under the White Mountain province and is isotopically similar to the mantle which gives rise to oceanic island basalts. In contrast, Pb isotopic ratios for the New England Seamount chain (TARAS and HART, 1983), which apparently represents the oceanic extension of this magmatic activity, are significantly more radiogenic. It is possible that a mantle plume provided the heat energy, and perhaps metasomatic fluids, to trigger melting in the subcontinental mantle, whereas in the case of the oceanic extension the plume directly contributed to the observed magmatism, as reflected in the more radiogenic Pb ratios.     

Lead isotopic compositions of Tonga-Kermadec volcanics and their petrogenetic significance

Lead isotopic compositions, and lead and uranium concentrations have been determined for samples from the Tongan islands of Late, Fonualei, Hunga-Ha'apai and Eua and for the Kermadec islands of Raoul, Macauley, Esperance and Napier. The Kermadec samples form a linear array in a Pb²⁰⁶/Pb²⁰⁴ vs Pb²⁰⁷/Pb²⁰⁴ plot which if interpreted in terms of a two stage mantle model indicates a mantle fractionation of Pb from U at about 1.2×10⁹ yr. The Tongan volcanics, except Eua, have a very narrow range of isotopic compositions, only slightly exceeding the experimental error limits. This is interpreted to be the result of efficient mixing of the mantle in response to rapid extension behind the Tongan arc. The rate of extension appears to determine whether convection mixing can occur, since the sub-Kermadec mantle which experienced slower extension is not well mixed isotopically. The isotopic compositions show no evidence for a component in the magma derived from sediments dragged down the Benioff zone. The pre-Eocene Eua volcanics have lead which is substantially more radiogenic than the younger Tongan volcanics and are interpreted as a sample of the mantle before convective mixing occurred.     

Rb-Sr and U-Th-Pb systematics of alkaline rocks: the alkaline rocks from Italy

The isotopic composition of Pb and Sr and the abundances of Rb, Sr, U, Th, and Pb were determined for whole rock samples from all major volcanic centres of the Cenozoic alkaline volcanism of Central and South Italy, together with some samples from the contemporaneous anatectic Tuscan volcanism. The Sr and Pb isotopic compositions of the alkaline rocks show a negative correlation combined with a regional trend: the ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios decrease from 0.711 in the north-west to 0.704 in the south-east, while the ${}^{206}\text{Pb}{}^{204}\text{Pb}$ ratios increase from 18.7 to 20.0. Variations in both isotopic compositions are generally small throughout erupted rock sequences for any volcanic centre.The Pb and Sr isotopic abundance variations are interpreted on the basis of two alternative models, which correspond to two groups of geological processes: variations can result (i) from a time dependent development in subsystems with different $\text{Rb}\text{Sr}$ or $\text{U(Th)}\text{Pb}$ ratios or, (ii) from mixing of Sr or Pb with different isotopic compositions. Combining both Pb and Sr isotope abundance measurements it is shown that the source of each volcanic centre is formed by various degrees of mixing between two components. One component and the most southern Tuscan anatectic rocks most likely have a common source, whereas the other component of the mixing process is suggested to be a liquid fraction derived from a small degree of partial fusion of a hydrous mantle. Thus at least a two-stage evolution of the Italian alkaline rocks is indicated: first a mixing process leading to the formation of the parental material followed by differentiation processes leading to the formation of the erupted rock sequences.The geodynamic model which explains the data best is that of a lateral inhomogeneous mantle. The lateral inhomogeneities in the mantle would be the result of mixing between originally mantle and crustal derived material. The mixing process itself would not have any primary connection with the Quarternary volcanic activity.     

Differences in lead isotope composition in the stratiform McArthur zinc-lead-silver deposit

Lead isotopic composition and uranium and lead concentrations have been determined for galena, sphalerite, pyrite and acetic acid soluble material from the McArthur area in order to test the hypothesis of a dual sulphur source suggested by the sulphur isotope data of Smith and Croxford (Sulphur isotope ratios in the McArthur lead-zinc-silver deposit, Nature Phys. Sci. 245, 10–12 (1973)). Galena, sphalerite and the acetic acid washes from the McArthur deposit have uniform isotopic ratios (²⁰⁶Pb/²⁰⁴Pb, 16.07–16.15; ²⁰⁷Pb/²⁰⁴Pb, 15.37–15.47; ²⁰⁸Pb/²⁰⁴Pb, 35.57–35.89) consistent with other conformable ore deposits, whereas the ratios for pyrite are variable and quite radiogenic (²⁰⁶Pb/²⁰⁴Pb, 16.24–16.49; ²⁰⁷Pb/²⁰⁴Pb, 15.42–15.58; ²⁰⁸Pb/²⁰⁴Pb, 35.82–36.98). Acid washes where dolomite is a major dissolved phase are also radiogenic. The lead in the pyrite appears to have been derived from at least two sources: the less radiogenic lead coming from an exhalative source as for galena and sphalerite and the more radiogenic lead probably being leached from the country rocks. It is proposed that analysis of pyrite for isotopic composition and concentration of lead could be used as an indicator for similar types of deposits in this area.     

Isotopic composition of phanerozoic ore leads from the Swedish segment of the Fennoscandian Shield

95 analyses of ore lead isotope ratios from 23 Phanerozoic ore deposits from the Swedish segment of the Fennoscandian Shield form a marked linear trend on a ²⁰⁷Pb/²⁰⁴Pb versus ²⁰⁶Pb/²⁰⁴Pb diagram. The line may be interpreted in a two-stage model, the lead being derived from 1.8±0.15 Ga old Svecokarelian basement and mineralization occurring at 0.4±0.15 Ga. The initial composition of the Svecokarelian rock lead was similar to the lead in early Proterozoic volcanogenic sulfide ores in Sweden. — The large spread in the isotope ratios was caused by a combination of selective leaching of different minerals in the source rocks, mixing with less radiogenic Caledonian lead, and local or regional variations in the U, Th and Pb contents of the basement. As a consequence, conventional methods of identifying source rocks from lead isotopic data (e.g. mu-values, Th/U ratios) may not be directly applicable. Phanerozoic ore lead development in the Swedish section of the Fennoscandian Shield was ensialic. That is, the ore lead was almost entirely derived from the Precambrian basement, although this basement does not appear to be anomalously enriched in Pb. No juvenile or mantle lead was apparently contributed to this section of the crust after the Precambrian, except for that mechanically transported onto the western edge of the Shield by the Caledonian nappes. However, some of Europe's largest lead deposits are included in these Swedish Phanerozoic mineralizations, suggesting that it was the nature of the processes involved rather than the richness of the source, that determined their formation.     

Assessment of geochemical anomalies for gold exploration using lead isotopes in west Hainan, China

Lead isotopic ratios and Pb contents have been measured along typical profiles across orebodies of the Baoban and Tuwaishan gold deposits on Hainan Island, China. These deposits are hosted by the middle to upper Proterozoic Baoban Group, which is composed of migmatite and extends for about 51 km on the hanging-wall side of the Gezhen Fault. The deposits have a common initial Pb isotopic ratio of ²⁰⁶Pb/²⁰⁴Pb = 18.683, but show distinctive variations within each deposit.The Pb isotopic ratios are more homogeneous in the orebodies and altered auriferous rocks than in the migmatite wall rocks. The richest orebody in the study area is known as the V1 orebody of the Baoban deposit; it has the lowest and most homogeneous ²⁰⁶Pb/²⁰⁴Pb ratio. This feature suggests that in this migmatitic area, it is possible to distinguish ores from barren wall rocks, and rich ore shoots from non-commercial mineralization, by their distinctive Pb isotopic ratios.A lower initial Pb isotopic ratio (²⁰⁶Pb/²⁰⁴Pb= 18.538) was measured in two other deposits, Beiniu and Erjia, which occur in the same migmatite and are controlled by the same fault as the Baoban and Tuwaishan deposits. Therefore, two metallogenic phases may have taken place, one at 85 Ma and the other at 170 Ma; these ages can be calculated using the Pb growth model of Cumming and Richards.The feasibility of evaluating geochemical anomalies through their Pb isotopic signatures was investigated by comparing the Pb isotopic ratios of B horizon soils from significant and non-significant anomalies with those obtained from the ores and alteration zone rocks. The results show that the Pb isotopic ratios in significant anomalies are consistent with those of the ores, whereas the signatures of non-significant anomalies are heterogeneous and rather different from those of the ores.Six unexplored anomalies have been evaluated using this criteria; five of them were found to be non-significant. One anomaly, however, presents the same signature as the Beiniu deposit, suggesting that it may be related to undiscovered ore close to the Gezhen Fault. Plans have been made to drill this target.     

Petrology and geochemistry of the Karaj Dam basement sill: Implications for geodynamic evolution of the Alborz magmatic belt

The northeastward subduction of the Neo-Tethyan oceanic lithosphere beneath the Iranian block produced vast volcanic and plutonic rocks that now outcrop in central (Urumieh–Dokhtar magmatic assemblage) and north–northeastern Iran (Alborz Magmatic Belt), with peak magmatism occurring during the Eocene. The Karaj Dam basement sill (KDBS), situated in the Alborz Magmatic Belt, comprises gabbro, monzogabbro, monzodiorite, and monzonite with a shoshonitic affinity. These plutonic rocks are intruded into the Karaj Formation, which comprise pyroclastic rocks dating to the lower–upper Eocene. The geochemical and isotopic signatures of the KDBS rocks indicate that they are cogenetic and evolved through fractional crystallization. They are characterized by an enrichment in LREEs relative to HREEs, with negative Nb–Ta anomalies. Geochemical modeling using Sm/Yb versus La/Yb and La/Sm ratios suggests a low-degree of partial melting of a phlogopite–spinel peridotite source to generate the KDBS rocks. Their low I_Sr = 0.70453–0.70535, ɛNd (37.2 Ma) = 1.54–1.9, and T_DM ages ranging from 0.65 to 0.86 Ga are consistent with the melting of a Cadomian enriched lithospheric mantle source, metasomatized by fluids derived from the subducted slab or sediments during magma generation. These interpretations are consistent with high ratios of ²⁰⁶Pb/²⁰⁴Pb = 18.43–18.67, ²⁰⁷Pb/²⁰⁴Pb = 15.59, and ²⁰⁸Pb/²⁰⁴Pb = 38.42–38.71, indicating the involvement of subducted sediments or continental crust. The sill is considered to have been emplaced in an environment of lithospheric extension due to the slab rollback in the lower Eocene. This extension led to localized upwelling of the asthenosphere, providing the heat required for partial melting of the subduction-contaminated subcontinental lithospheric mantle beneath the Alborz magmatic belt. Then, the shoshonitic melt generates the entire spectrum of KDBS rocks through assimilation and fractional crystallization during the ascent of the magma.     

Source contamination and mantle heterogeneity in the genesis of Italian potassic and ultrapotassic volcanic rocks: Sr–Nd–Pb isotope data from Roman Province and Southern Tuscany

Summary The Tyrrhenian border of the Italian peninsula has been the site of intense magmatism from Pliocene to recent times. Although calc-alkaline, potassic and ultrapotassic volcanism overlaps in space and time, a decrease of alkaline character in time and space (southward) is observed. Alkaline ultrapotassic and potassic volcanic rocks are characterised by variable enrichment in K and incompatible elements, coupled with consistently high LILE/HFSE values, similar to those of calc-alkaline volcanic rocks from the nearby Aeolian arc. On the basis of mineralogy and major and trace element chemistry two different arrays can be recognised among primitive rocks; a silica saturated trend, which resulted in formation of leucite-free mafic rocks, and a silica undersaturated trend, charactrerised by leucite-bearing rocks. Initial ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd values of Italian ultrapotassic and potassic mafic rocks range from 0.70506 to 0.71672 and from 0.51173 to 0.51273, respectively. ²⁰⁶Pb/²⁰⁴Pb values range between 18.50 and 19.15, ²⁰⁷Pb/²⁰⁴Pb values range between 15.63 and 15.70, and ²⁰⁸Pb/²⁰⁴Pb values range between 38.35 and 39.20. The general ε_Sr vs. ε_Nd array, along with crustal lead isotopic values, clearly indicates that a continental crustal component has played an important role in the genesis of these magmas. The main question is where this continental crustal component has been acquired by the magmas. Volcanological and petrologic data indicate continental crustal contamination to be a leading process along with fractional crystallisation and magma mixing. Considering, however, only the samples thought to represent primary magmas, which have been in equilibrium with their mantle source, a clearer picture emerges. A large variation of ε_Sr vs. ε_Nd is still observed, with ε_Sr from −2 to +180 and ε_Nd from + 2 to −12. A bifurcation of this array is observed in the samples that plot in the lower right quadrant, with mafic leucite-bearing Roman Province rocks buffered at ε_Sr = + 100 whereas the mafic leucite-free potassic and ultrapotassic rocks point to strongly radiogenic Sr compositions. We may argue that mafic leucite-bearing Roman Province rocks point to ε_Sr and ε_Nd values similar to those of Miocene carbonate sediments whereas mafic leucite-free potassic and ultrapotassic rocks point to a silicate upper crust end-member. Lead isotopes plot well inside the field of island arcs, overlapping the values of pelagic sediments as well, but bifurcation between the samples north and south of Rome is observed. The main characteristic for the mantle source of Italian potassic and ultrapotassic magmas is the clear upper crustal signature acquired prior to partial melting through metasomatic agents released by the subducted slab. In addition, one lithospheric mantle source in the north and an asthenospheric mantle source, pointing to an HIMU reservoir, in the south were recognised. The chemical and isotopic differences observed between the northern and southern sectors of the magmatic region were possibly due to the presence of a carbonate-rich component in the crustal enriching agent in the south. One crustal component might have been generated by melting of silicate metasedimentary rocks or sediments from an ancient subducted slab. The second one might reflect the activity of mostly CO₂-rich fluid released more recently by the incipient subduction of carbonate sedimentary rocks. Received February 16, 2000; revised version accepted September 6, 2001     

Isotopic composition of strontium in three basalt-andesite centers along the Lesser Antilles arc

Si⁸⁷/Sr⁸⁶ ratios have been determined for lavas and py lastic rocks from three basalt-andesite centers along the Lesser Antilles arc—Mt. Misery on the island of St. Kitts, Soufriere on the island of St. Vincent, and Carriacou, an island of The Grenadines. The average Si⁸⁷/Sr⁸⁶ content of these rocks is 0.7038 for Mt. Misery, 0.7041 for Soufriere, and 0.7053 for Carriacou. All the Sr⁸⁷/Sr⁸⁶ values from each center are the same within analytical uncertainty (±0.0002). The constancy of strontium isotopic data within each center supports the hypothesis that basalts and andesites for each specific center investigated are generated from the same source — in agreement with petrographic and major- and minor-element data. Strontium isotopic compositions and elemental concentrations, particularly of strontium and nickel, indicate that this source was mantle peridotite and that the relationship between the respective basalts and andesites is probably fractional crystallization.Publication authorized by the Director, U.S. Geological Survey.     

Lead isotope constraints on the genesis of Pb–Zn deposits in the Neoproterozoic Vazante Group, Minas Gerais, Brazil

The Neoproterozoic Vazante Group at the western border of the São Francisco Craton, Brazil, hosts the largest Zn–Pb district in South America. Several authors have classified this mineral district as Mississippi Valley-type (MVT), based on the intimate association with carbonates and the epigenetic character of most ore bodies. In this paper, we present 47 new lead isotope data from four deposits located along the 300 km N–S Vazante–Paracatu–Unai linear trend. Pb isotope ratios indicate sources with relatively high U/Pb and Th/Pb ratios. Considering the ²⁰⁶Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb ratios as indicative parameters for the source, we suggest an upper crustal source for the metals. The small variation on the Pb isotope ratios compared to those observed in the classical MVT deposits, and other geological, fluid inclusion and sulphur isotopic data indicates a metallogenic event of long duration. It was characterized by focused circulation of hydrothermal fluids carrying metals from the basement rocks and from the sedimentary pile. The data obtained are more compatible with an evolution model similar to that of IRISH-type deposits. The existence of three Pb isotopic populations could be the result of regional differences in composition of the source rocks and in the fluid–rock interaction since the mineralization is a long-term process.