Pb isotopes in Ascension Island rocks: oceanic origin for the gabbroic to granitic plutonic xenoliths

The Pb isotopic compositions and U and Pb concentrations of the lava series (alkali basalt to comendite) and of their plutonic xenoliths (gabbro to alkaline granite) of Ascension Island are reported. The data are used to evaluate the source of the xenoliths which formed two differentiation suites: the acidic and intermediate xenoliths together with most of the lavas on the one hand, and the gabbroic xenoliths and a basaltic tuff on the other hand. The Pb isotopic compositions imply a mantle origin for the source magmas of the xenoliths and confirm the possibility of generating granitic rocks in an oceanic environment by fractional crystallization of a mantle-derived magma whose geochemical and isotopic characteristics are comparable to the source magmas of oceanic island basalts.     

Isotopic composition of lead and strontium in lavas and coarse-grained blocks from Ascension Island,South Atlantic

New Sr and Pb isotope data are presented for a selection of lavas and associated coarse-grained blocks from Ascension Island. K-Ar dates for the lavas range up to1.5±0.2Ma. Initial⁸⁷Sr/⁸⁶Sr ratios are consistent with earlier measurements and for most rocks are ca. 0.7029, but range up to 0.7135 in the case of the most evolved lavas and blocks. Pb isotope data are also consistent with earlier measurements, but the Pb in two gabbroic blocks is less radiogenic than Pb in the other rocks. It is suggested that these gabbroic blocks crystallized from a magma of tholeiitic composition whose source was similar to that of mid-oceanic ridge basalt whereas the lavas and other blocks crystallized from mildly alkaline magmas derived from a source further from the crest of the Mid-Atlantic Ridge. The high⁸⁷Sr/⁸⁶Sr ratios result from contamination of the most silicic magma by radiogenic Sr from pelagic sediments. These data and their interpretation are consistent with the petrological and geochemical observations that the granite blocks are the coarse-grained equivalents of the volcanic suite [11] and not fragments of relict continental material [2,3].     

A Nd,Sr and O isotopic investigation into the causes of chemical and isotopic zonation in the Bishop Tuff,California

The Bishop Tuff represents a single eruption of chemically zoned rhyolitic magma. Six whole rock samples spanning the compositional and temperature range yield initial⁸⁷Sr/⁸⁶Sr of 0.7060–0.7092 andδ¹⁸O of 5.9–10.3‰. Six constituent sanidines yield smaller ranges of initial⁸⁷Sr/⁸⁶Sr of 0.7061–0.7069 andδ¹⁸O of 6.7–7.9. In contrast¹⁴³Nd/¹⁴⁴Nd ratios for the six whole rocks and two constituent magnetites exhibit negligible variation with a mean of0.51258 ± 1. These data are used to show that the phenocrysts were precipitated from an already chemically zoned liquid, that the zoning process involved negligible assimilation of, or exchange with, country rocks and that the extreme Sr and O isotopic disequilibria are probably the result of post-eruptive interaction with meteoric water. The parent magma had?Nd = ?0.9, ?Sr = +23 andδ¹⁸O = 7‰ and was formed from mantle-derived magmas and/or melts of lower crustal rocks isotopically similar to parts of the Sierra Nevada Batholith.     

The Sr, Nd and O isotopic studies of the 1991–1995 eruption at Unzen, Japan

The magma generation at Unzen volcano may be considered as the product of crustal material mixed with mantle magma accompanied by fractional crystallization (AFC). The magma in the Unzen volcano is estimated to consist of about 50–80% of residual magma (F) and about 30–70% assimilated crustal material (A) relative to the original magma. Concerning the 1991–1995 eruption, it is estimated that the magma formed as the result of mixing of about 50–60% crustal material and about 55–65% of residual magma. An alternative magma eruption model for the 1991–1995 eruption is proposed here. In the early stage, the isotopic characteristics of 1991 eruption are defined by AFC process in the deeper magma chamber. Later, the magma ascended through the conduit and quiescently stayed for a long time in a shallow reservoir before eruption. The minerals continuously crystallized as phenocrysts especially at the chilled top and outer margin in the shallow chamber. The crystallized phenocryst mush was reworked into the central part of the magma chamber by means of magma convection and rapid magma ascent. Therefore, the reaction between phenocrysts and melt occurs only in internal chemical disequilibrium in the magma chamber. In contrast, the isotopic compositions of the original magma shall be little influenced by the above processes throughout its eruptive history. The 1991–1995 eruptive rocks of the Unzen volcano show their characteristics in Sr and Nd isotopic values independent of their two previous eruptions. However, the isotopic values of early eruptive product could represent the original magma value. This result also supports the previous work of Chen et al. (1993) [Chen, C.H., DePaolo, D.J., Nakada, S., Shieh, Y.N., 1993. Relationship between eruption volume and neodymium isotopic composition at Unzen volcano. Nature 362, 831–834], that suggested the Nd of early or precursory eruptive products could be a qualitative indicator of the maximum size of a continuing or impending eruption.     

Large scale isotopic Sr, Nd and O isotopic anatomy of altered oceanic crust: DSDP/ODP sites417/418

Large-scale compositional domains at DSDP/ODP drill sites 417A, 417D and 418A were analyzed for O, Sr and Nd isotope ratios, and REE, U, K, Rb and Sr abundances, to constrain the bulk chemical composition of the oceanic crust that is recycled at subduction zones. The combination of the three sites gives the composition of the upper oceanic crust in this region over a distance of about 8 km. The δ¹⁸O_SMOW and⁸⁷Sr/⁸⁶Sr_meas of compositional domains 10–100 m in size correlate well, with a range of 7.7–19.2 and 0.70364–0.70744, and mean of 9.96 and 0.70475, respectively. The Rb inventory of the upper crust increases by about an order of magnitude, while Sr contents remain constant. U abundances increase moderately under oxidizing alteration conditions and nearly triple in the commonly reducing alteration environments of the upper oceanic crust. REEs are influenced by alteration only to a small extent, and recycled oceanic crust is similar to MORB with respect to¹⁴³Nd/¹⁴⁴Nd. Even though the average composition of the upper oceanic crust is well defined, the large scale composition varies widely. Highly altered compositional domains may not have a large impact on the average composition of the oceanic crust, but they may preferentially contribute to fluids or partial melts derived from the crust by prograde metamorphic reactions.     

Isotopic composition of lead and strontium in lavas and coarse-grained blocks from Ascension Island,South Atlantic—an addendum

Natural marokite (CaMn₂O₄) has been studied at high pressures and temperatures using a diamond-anvil press coupled with laser heating in the pressure range 100–250 kbar. A mixture of marokite, CaMnO₃ (perovskite) and MnO (rocksalt) has been observed in all runs in the above pressure range by X-ray diffraction study of the quenched samples. It was interpreted that marokite disproportionates into the mixture CaMnO₃ (perovskite) + MnO (rocksalt) at pressures below 100 kbar. A general comparison of the molar volume for all known compounds having the marokite-related structures (including CaFe₂O₄ and CaTi₂O₄) with those for a mixture of perovskite plus rocksalt structures suggested that the mixture is more stable than the marokite-related structures at high pressures, as confirmed by the present experimental result. The CaFe₂O₄-modification of common nepheline (NaAlSiO₄) is also suggested to be unstable relative to the component oxides of α-NaAlO₂ + SiO₂ (stishovite) at high pressures.     

The NdSr isotopic correlation in mantle materials and geodynamic consequences

The neodymium-strontium isotopic correlation observed in most of the Earth mantle materials is evaluated by means of direct modelling. Several geochemical models are quantitatively developed to explain the observations. The main results of this modelling are that such a correlation is not geochemically trivial and that it corresponds to specific conditions in chemical fractionation. These specific conditions seem to be satisfied by solid-liquid partitioning in magmatic conditions. The discussion of the experimental data supports a continuous convecting-magmatic fractionation model for a large proportion of the mantle.     

A Nd and Sr isotopic study of the Trinity peridotite; implications for mantle evolution

Field evidence indicates that the Trinity peridotite was partially melted during its rise as a part of the upwelling convecting mantle at a spreading center. A SmNd mineral isochron for a plagioclase lherzolite yields an age,T = 427 ± 32 Ma and initialε_Nd = + 10.4 ? 0.4 which is distinctly higher than that expected for typical depleted mantle at this time. This age is interpreted as the time of crystallization of trapped melt in the plagioclase lherzoliteP-T field. This time of crystallization probably represents the time when the massif was incorporated as a part of the oceanic lithosphere. The SmNd model age of the plagioclase lherzolite totalrock isT_CHUR^Nd = 3.4 AE. This suggests that the Trinity peridotite was derived from a mantle that was depleted rather early in earth history. The peridotite contains many generations of pyroxenite dikes and some microgabbro dikes. We report data for two dikes that clearly crosscut the main metamorphic fabric of the peridotite. A microgabbro dike yields a SmNd mineral isochron age ofT = 435 ± 21 Ma andε_Nd = + 6.7 ? 0.3. A pyroxenite dike yields an initialε_Nd = + 7.3 ± 0.4. The initialε_Nd values for the pyroxenite and gabbro dikes are fairly similar to those for the depleted mantle at this time and are distinct from the lherzolite—demonstrating that they are not genetically related. RbSr data do not give any coherent pattern. However, some bounds can be put on initial Sr values ofε_Sr ? ?21 for the plagioclase lherzolite andε_Sr ? ?8.7 for the microgabbro dike. It is plausible that the dikes represent cumulates left behind from island arc magmas that rose through the the oceanic lithosphere within the vicinity of a subduction zone. Major and trace elements and SmNd isotopic data indicate a multiple stage history for the Trinity peridotite; a small melt fraction was extracted from an undepleted source ～ 3.4 AE or more ago to produce the proto-lherzolite; a large fraction of melt (～ 12 to 23%) was extracted from the proto-lherzolite to produce the present rock; the lherzolite was then crosscut by dikes from average depleted mantle ～ 0.44 AE ago. The data are compatible with the depleted mantle source being formed very early in earth history. Although most available data indicate that the depleted upper mantle has been relatively well stirred through time, the Trinity data suggest that very ancient Nd isotopic values are preserved and thus chemical and physical heteorgeneities are sometimes preserved in the depleted source of mid-ocean ridge basalts as well as the oceanic lithosphere which they intrude.     

Possible origin of K-rich volcanic rocks from Virunga,East Africa,by metasomatism of continental crustal material: Pb,Nd and Sr isotopic evidence

The isotopic compositions of Sr, Nd and Pb together with the abundances of Rb, Sr, U and Pb have been determined for mafic and felsic potassic alkaline rocks from the young Virunga volcanic field in the western branch of the East African rift system.⁸⁷Sr/⁸⁶Sr varies from 0.7055 to 0.7082 in the mafic rocks and from 0.7073 to 0.7103 in the felsic rocks. The latter all come from one volcano, Sabinyo. Sabinyo rocks have negative ε_Ndvalues ofε_Nd = ?10. Nd and Sr isotopic variations in the basic potassic rocks are correlated and plot between Sabinyo and previously reported [1] compositions (ε_Nd = +2.5;⁸⁷Sr/⁸⁶Sr≈ 0.7047) for Nyiragongo nephelinites. The Pb isotopic compositions for Sabinyo rocks are nearly uniform and average²⁰⁶Pb/²⁰⁴Pb≈ 19.4,²⁰⁷Pb/²⁰⁴Pb= 15.79–15.84,²⁰⁸Pb/²⁰⁴Pb≈ 41.2. The basic potassic rocks have similar²⁰⁶Pb/²⁰⁴Pb values but range in²⁰⁷Pb/²⁰⁴Pb and²⁰⁸Pb/²⁰⁴Pb from the Sabinyo values to less radiogenic compositions.Excellent correlations of⁸⁷Sr/⁸⁶Sr with Rb/Sr, 1/Sr and²⁰⁷Pb/²⁰⁶Pb for Sabinyo rocks suggest these to be members of a hybrid magma series. However, the nearly uniform Pb compositions for this series points to radiogenic growth of⁸⁷Sr in the magma source region following an event which homogenized the isotopic compositions but not Rb/Sr. The Rb-Sr age derived from the erupted Sabinyo isochron-mixing line is consistent with the ～500 Myr Pb-Pb age from Nyiragongo [1], which suggests that this event affected all Virunga magma sources. The event can again be traced in the Pb-Pb, Pb-Sr and Nd-Sr isotopic correlations for all Virunga rocks, including Nyiragongo, when allowances are made for radiogenic growth subsequent to this mixing or incomplete homogenization event. Inferred parent/daughter element fractionations point to a metasomatic event during which a mantle fluid invaded two lithospheric reservoirs: a +ε_Nd reservoir sampled by the Nyiragongo nephelinites and suggested to be the subcontinental mantle and a ?ε_Nd reservoir sampled by the mafic and felsic potasssic volcanism. Whether this ?ε_Nd reservoir is the crust, continental crustal material in the mantle or anomalous mantle cannot be decided from the data. The simplest answer, that this reservoir is the continental crust, seems to be at variance with experimental evidence suggesting a subcrustal origin for basic potassic magmas. Partial melting of the ancient metasomatised lithospheric domains and ensuing volcanism seems to be entirely a response to decompression and rising geotherms during rifting and thinning of the lithosphere.     

The origin of Samoa: new evidence from Sr, Nd, and Pb isotopes

We report Sr, Nd and Pb isotope ratios and parent and daughter element concentrations in 34 volcanic rocks from Samoa. The highly undersaturated post-erosional volcanics, which have erupted in Recent to Historic time along a 250-km-long fissure, have isotopic compositions that define fields distinct from those of the tholeiitic to alkalic lavas of the older Samoan shield volcanoes. Most shield lavas have²⁰⁶Pb/²⁰⁴Pb of 18.9–19.4,⁸⁷Sr/⁸⁶Sr of 0.7045–0.7055 and⁸⁷Sr/⁸⁶Sr (to 0.7075). In general, isotopic compositions of the shield lavas are similar to those of the Marquesas and Society Islands. Post-erosional samples have lower²⁰⁶Pb/²⁰⁴Pb and¹⁴³Nd/¹⁴⁴Nd and higher⁸⁷Sr/⁸⁶Sr than most shield lavas. The most striking feature of the post-erosional data is a negative correlation between²⁰⁷Pb/²⁰⁴Pb and²⁰⁶Pb/²⁰⁴Pb. This suggests that post-erosional lavas are derived from mixtures of the shield source and a high-²⁰⁷Pb/²⁰⁴Pb,⁸⁷Sr/⁸⁶Sr, low-²⁰⁶Pb/²⁰⁴Pb and¹⁴³Nd/¹⁴⁴Nd post-erosional source which may contain recycled ancient sediment. This enriched mantle domain may also underlie the Ontong-Java and Manihiki Plateaus to the north and west. Although both the Samoan shield and post-erosional lavas show chemical characteristics often associated with mantle plumes, only the shield volcanism can plausibly be related to a plume. The post-erosional eruptions appear to be the result of flexure and rifting due to plate bending at the northern termination of the Tonga Trench.     

Lead concentration and isotopic composition in five peridotite inclusions of probable mantle origin

The lead content of five whole-rock peridotite inclusions (four lherzolites and one harzburgite) in alkali basalt ranges from 82 to 570 ppb (parts per billion). Approximately 30–60 ppb of this amount can be accounted for by analyzed major silicate minerals (olivine ≤ 10 ppb; enstatite 5–28 ppb; chrome diopside ～400 ppb). Through a series of acid leaching experiments, the remainder of the lead is shown to be quite labile and to reside in either glassy or microcrystalline veinlets or accessory mineral phases, such as apatite and mica. The lead isotopic composition of the peridotites (²⁰⁶Pb/²⁰⁴Pb= 18.01–18.90;²⁰⁷Pb/²⁰⁴Pb= 15.52–15.61;²⁰⁸Pb/²⁰⁴Pb= 37.80–38.86) lies within the range of values defined by many modern volcanic rocks and, in particular, is essentially coextensive with the abyssal tholeiite field. In all but one instance, isotopic differences were found between the peridotite and its host alkali basalt. Two of the peridotites clearly demonstrated internal isotopic heterogeneity between leachable and residual fractions that could not simply be due to contamination by the host basalt. However, there is no evidence that these ultramafic rocks form some layer in the mantle with isotopic characteristics fundamentally different from those of the magma sources of volcanic rocks.     

D/H ratios in speleothem fluid inclusions: A guide to variations in the isotopic composition of meteoric precipitation?

D/H ratios of fluid inclusion waters extracted from²³⁰Th/²³⁴U-dated speleothems that were originally deposited under conditions of isotopic equilibrium should provide a direct estimate of the hydrogen isotopic composition of ancient meteoric waters. We present here D/H ratios for 47 fluid inclusion samples from thirteen speleothems deposited over the past 250,000 years at cave sites in Iowa, West Virginia, Kentucky and Missouri. At each site glacial-age waters are depleted in deuterium relative to those of interglacial age. The average interglacial/glacial shift in the hydrogen isotopic composition of meteoric precipitation over ice-free areas of east-central North America is estimated to be ?12‰. This shift is consistent with the present climatic models and can be explained in terms of the prevailing pattern of atmospheric circulation and an increased ocean-continent temperature gradient during glacial times which more than compensated for the increase in deuterium content of the world ocean.     

Geochemical and Sm–Nd isotopic characteristics of metabasites from central Hainan Island, South China and their tectonic significance

Abstract   Major and trace elements and Sm–Nd isotopic data are presented for metabasites that are present as lenses within Paleozoic metasediments in the Chenxing and Bangxi regions, central Hainan Island, Southeast (SE) China. Most metabasites are metamorphosed cumulated gabbroic rocks tholeiitic in nature, and characterized by varying degrees of depletion in Th, Nb, Ta and light rare earth elements (LREE). Moreover, they show high positive ∈Nd(T) values of approximately +7, similar to those of mid-ocean ridge basalts (MORB). A Sm–Nd isochron age of 333 ± 12 Ma obtained for the metabasites is interpreted as their crystallization age. The combined geochemical and Sm–Nd isotopic data suggest that the metabasites were generated by dynamic partial melting from a MORB-like mantle source in an oceanic regime. These rocks probably represent remnants of fragmented oceanic crust of the eastern part of Paleo-Tethys. They were obducted onto the continental crust as part of the 'Shilu Mélange' in earliest Mesozoic time when southern Hainan (part of the Indochina block) collided with northern Hainan (part of South China). Alternatively, they could be formed in a volcanic rifted passive margin at the sea-floor spreading stage as part of MORB-like seaward-dipping reflector break-up packages.     

Major element, REE, and Pb, Nd and Sr isotopic geochemistry of Cenozoic volcanic rocks of eastern China: implications for their origin from suboceanic-type mantle reservoirs

Major- and rare-earth-element (REE) concentrations and UThPb, SmNd, and RbSr isotope systematics are reported for Cenozoic volcanic rocks from northeastern and eastern China. These volcanic rocks, characteristically lacking the calc-alkaline suite of orogenic belts, were emplaced in a rift system which formed in response to the subduction of the western Pacific plate beneath the eastern Asiatic continental margin. The rocks sampled range from basanite and alkali olivine basalt, through olivine tholeiite and quartz tholeiite, to potassic basalts, alkali trachytes, pantellerite, and limburgite. These rock suites represent the volcanic centers of Datong, Hanobar, Kuandian, Changbaishan and Wudalianchi in northeastern China, and Mingxi in the Fujian Province of eastern China.The major-element and REE geochemistry is characteristic of each volcanic suite broadly evolving through cogenetic magmatic processes. Some of the outstanding features of the isotopic correlation arrays are as follows: (1) NdSr shows an anticorrelation within the field of ocean island basalts, extending from the MORB end-member to an enriched, time-averaged high Rb/Sr and Nd/Sr end-member (EM1), (2) SrPb also shows an anticorrelation, similar to that of Hawaiian and walvis Ridge basalts, (3) NdPb shows a positive correlation, and (4) the ²⁰⁷Pb/²⁰⁴Pb vs ²⁰⁶Pb/²⁰⁴Pb plot shows linear arrays parallel to the general trend (NHRL) for MORB on both sides of the geochron, although in the ²⁰⁸Pb/²⁰⁴Pb vs ²⁰⁶Pb/²⁰⁴Pb plot the linear array is significantly displaced above the NHRL in a pattern similar to that of the oceanic island basalts that show the Dupal signatures. In all isotope correlation patterns, the data arrays define two different mantle components—a MORB-like component and an enriched mantle component. The isotopic data presented here clearly demonstrate the existence of Dupal compositions in the sources of the continental volcanic rocks of eastern China. We suggest that the subcontinental mantle beneath eastern China served as the reservoir for the EMI component, and that the MORB component was either introduced by subduction of the Kula-Pacific Ridge beneath the Asiatic plate in the Late Cretaceous, as proposed by Uyeda and Miyashiro, or by upwellings in the subcontinental asthenosphere due to subduction.     

Aeolian island arc (South Tyrrhenian Sea) magma heterogeneites in historical lavas: Sr and Pb isotopic evidence

Historical volcanic rocks of the Aeolian islands range in composition from shoshonitic basalts to rhyolites, which might reflect fractional crystallization of a shoshonitic parent magma. However Sr and Pb isotopic data indicate a more complex history. The shoshonitic basalts at present erupted at Stromboli, although chemically similar to the postulated parent magma, are genetically unrelated to the other studied rocks. Sr isotopes indicate that Vulcano, Vulcanello and Lipari had independent magma sources. It is proposed that crustal contamination raised the Sr isotopic composition of the Lipari rhyolites. The rocks of these island are related by a common very steep trend of²⁰⁷Pb/²⁰⁴Pbvs. ²⁰⁶Pb/²⁰⁴Pb. Such a trend is a common feature of orogenic magmas and shows that Pb was derived by mixing of at least two components. Presently it is impossible to constrain precisely either the timing or the physical meaning of the Pb end members. The Pb isotopic trend in the Eolian island is very distinct from those recorded in volcanic rocks both from behind the arc (Etna, Iblean Mts.) and from Central and Southern Italy.     

Pb, Nd, and Sr isotopic constraints on the origin of Miocene basaltic rocks from northeast Hokkaido, Japan: Implications for opening of the Kurile back-arc basin

Late Miocene (7–9 Ma) basaltic rocks from the Monbetsu‐Kamishihoro graben in northeast Hokkaido have chemical affinities to certain back‐arc basin basalts (referred to herein as Hokkaido BABB). Pb‐, Nd‐ and Sr‐isotopic compositions of the Hokkaido BABB and arc‐type volcanic rocks (11–13 Ma and 4–4.5 Ma) from the nearby region indicate mixing between the depleted mantle and an EM II‐like enriched component (e.g. subducted pelagic sediment) in the magma generation. At a given ⁸⁷Sr/⁸⁶Sr, Hokkaido BABB have slightly lower ¹⁴³Nd/¹⁴⁴Nd and slightly less radiogenic ²⁰⁶Pb/²⁰⁴Pb compared with associated arc‐type lavas, but both these suites are difficult to distinguish solely on the basis of isotopic compositions. These isotopic data indicate that while generation of the Hokkaido BABB involves smaller amounts of the EM II‐like enriched component than do associated arc lavas, Hokkaido BABB are isotopically distinct from basalts produced at normal back‐arc basin spreading centers. Instead, northeast Hokkaido BABB are more similar to basalts erupted during the initial rifting stage of back‐arc basins. The Monbetsu‐Kamishihoro graben may have developed in association with extension that formed the Kurile Basin, suggesting that opening of the basin continued until late Miocene (7–9 Ma).     

The Shabogamo Intrusive Suite,Labrador: Sr and Nd isotopic evidence for contaminated mafic magmas in the Proterozoic

The Shabogamo Intrusive Suite comprises numerous bodies of variably metamorphosed gabbro which intrude Archean and Proterozoic sequences at the junction of the Superior, Churchill, and Grenville structural provinces in western Labrador. Combined Sm-Nd and Rb-Sr systematics in two bodies, ranging from unmetamorphosed to lightly metamorphosed, document a crystallization age of about 1375 m.y., and suggest that both bodies crystallized from magmas with similar Nd and Sr isotopic compositions. This age is in accordance with the existence of a regional magmatic event in the Churchill Province at approximately 1400 m.y.Rb-Sr systematics in two bodies of amphibolite-grade gabbro suggest a regional metamorphic event at about 950 m.y., corresponding to the waning stages of Grenville activity. Sm-Nd systematics in these high-grade bodies are affected to a much lesser degree than Rb-Sr.Initial ratios for¹⁴³Nd/¹⁴⁴Nd and⁸⁷Sr/⁸⁶Sr are lower and higher, respectively, than bulk earth values at 1375 m.y. Both these displacements are in the direction of older crustal material at 1375 m.y., and a model is proposed to produce the Shabogamo magma by mixing a mantle-derived magma with a partial melt of crustal rocks (approximately 4: 1 by volume). Young volcanic rocks with anomalous Nd and Sr isotopic ratios, which have previously been taken as evidence for “enriched” mantle, may be interpreted similarly.     

Triassic alkaline intrusives in the Yanliao-Yinshan area: their chronology, Sr, Nd and Pb isotopic characteristics and their implication

Dated isotopic ages for 15 alkaline intrusives in the Yanliao-Yinshan area, ranging from 268 to 190 Ma, ten of which are from 250 to 208 Ma, indicate that most of them were formed in the Triassic Epoch. All the E_Nd(t) ratios from - 17.19 to -3.21 averaging -7.09, the E_Sr(t) ratios fmm 11.7 to71.5 averaging 36.63, and the I_sr(t) ratios from 0.705 0 to 0.709 3 averaging 0.706 8, show their characteristics of enrichment. On the E_Nd (t) virus E_Sr(t) correlation diagram, the samples from these intmsives were plotted within the enriched mantle trend lines and just outside, demonstrating their close connection to materials from the enriched mantle reservoir, taking into account the same Pb isotopic composition as that of the mantle.