Age of the Archean Talga-Talga Subgroup, Pilbara Block, Western Australia, and early evolution of the mantle: new SmNd isotopic evidence

Archean komatiites, high-Mg basalts and tholeiites from the North Star Basalt and the Mount Ada Basalt formations of the Talga-Talga Subgroup, Warrawoona Group, Pilbara Block, Western Australia, define a linear correlation on the normal¹⁴³Nd/¹⁴⁴Nd vs.¹⁴⁷Sm/¹⁴⁴Nd isochron plot. The data give an age of 3712 ± 98 Ma and initialε_Nd(T) of +1.64 ± 0.40. The 3712 ± 98 Ma date is consistent with the regional stratigraphic sequence and available age data and the SmNd linear array may be interpreted as an isochron giving the eruption age of the Talga-Talga Subgroup. An alternative interpretation is that the isochron represents a mixing line giving a pre-volcanism age for the Subgroup. Consideration of geochemical and isotopic data indicates that the true eruptive age of the Talga-Talga Subgroup is possibly closer to about 3500 Ma. Regardless of the age interpretation, the new Nd isotopic data support an existence of ancient LREE-depleted reservoirs in the early Archean mantle, and further suggest that source regions for the Pilbara volcanic rocks were isotopically heterogeneous, withε_Nd(T) values ranging from at least 0 to +4.0.     

Geochemical characteristics of Yamadağı volcanics in central east Anatolia: an example from collision-zone volcanism

Neogene Yamadağı volcanic rocks consist of basaltic trachyandesite, trachyandesite, andesite, and dacite. The major- and trace-element chemistry indicates that the lavas are dominantly calc-alkaline and mildly alkaline in character, sodic in nature, and intermediate to acidic in composition. REE and trace-element patterns of volcanic rocks are similar to those typical of within plate magmatics. Volcanic rocks have low ⁸⁷Sr/⁸⁶Sr (0.70389–0.70633) and high ¹⁴³Nd/¹⁴⁴Nd ratios (0.51267–0.51276) and mostly plot within the mantle array of the isotope ratio diagram. The linear correlations among ⁸⁷Sr/⁸⁶Sr−¹⁴³Nd/¹⁴⁴Nd, SiO₂−⁸⁷Sr/⁸⁶Sr and SiO₂−¹⁴³Nd/¹⁴⁴Nd isotope ratios in the volcanics suggest that fractional crystallization combined with minor assimilation was an important process within the collision zone.     

Textural, isotopic and REE variations in spinel peridotite xenoliths, Massif Central, France

Sr and Nd isotope analyses and REE patterns are presented for a suite of well-documented mantle-derived xenoliths from the French Massif Central. The xenoliths include spinel harzburgites, spinel lherzolites and some pyroxenites. They show a wide range of textures from undeformed protogranular material through porphyroclastic to equigranular and recrystallised secondary types. Textural differences are strongly linked to trace element geochemistry and variations in radiogenic isotope ratios. Many undeformed protogranular xenoliths are Type IA LREE-depleted with MORB-type ε_Sr values between − 30.7 and − 23.6, and ε_Nd values + 13.9 to + 9.4. A second group of undeformed xenoliths are Type IB LREE-enriched with higher ε_Sr values (− 22.7 to − 10.6) and lower ε_Nd values (+ 11.9 to + 5.6). Deformed xenoliths with porphyroclastic, equigranular and secondary recrystallised textures are all Type IB (LREE-enriched, ε_Nd < 6.4, ε_Sr > 11.8). It is proposed that two separate events have given rise to the observed mixing arrays: (1) MORB-source depleted mantle was enriched by a component derived from an enriched mantle. Deformation and recrystallisation accompanied this event. (2) Subsequently, unenriched MORB-source mantle interacted with magmas chemically akin to the host basalts, and enrichment occurred with little deformation. Hypotheses of Tertiary mantle diapirism resulting in isochemical deformation and refinement of protogranular mantle to equigranular mantle are untenable because of differences in REE patterns and isotopic ratios between different textural groups.     

Isotopic geochemistry of Fernando de Noronha

Volcanic and hypabyssal rocks ranging in age from 12 to 3 Ma from the Fernando de Noronha archipelago in the western equatorial Atlantic Ocean can generally be divided into two age-compositional groups that have variable and distinct isotopic compositions. Predominantly older alkali basalts and trachytes are generally characterized by more radiogenic Sr-isotopic (⁸⁷Sr/⁸⁶Sr= 0.70457–0.70485) compositions and less radiogenic Nd-isotopic (¹⁴³/Nd¹⁴⁴Nd= 0.51271–0.51281) and Pb-isotopic (²⁰⁶Pb/²⁰⁴Pb= 19.132–19.282) compositions relative to the generally younger, more alkaline Si-undersaturated rocks which include nephelinites, ankaratrites, and melilitites (⁸⁷Sr/⁸⁶Sr= 0.70365–0.70418,¹⁴³Nd/¹⁴⁴Nd= 0.51277–0.51290,²⁰⁶Pb/²⁰⁴Pb= 19.317–19.565). These variations suggest the influence of at least two separate components in the source(s) of both series. One component is characterized by highRb/Sr and low μ, possibly derived from delaminated subcontinental lithosphere, whereas the other has high μ and lowRb/Sr similar to the source of St. Helena lavas. A third component is suggested by correlated compositions in the latest alkaline, Si-undersaturated lavas, and this component may be derived from depleted mantle. These isotopic variations in conjunction with the generally increasing degree of alkalinity with time are consistent with the temporal depletion of a low-μ, highRb/Sr component and increasing contributions from a high-μ component in the sources of the volanic rocks of Fernando de Noronha.     

Geochemical approach to magmatic evolution of Mt. Erciyes stratovolcano Central Anatolia, Turkey

Erciyes stratovolcano, culminating at 3917 m, is located in the Cappadocian region of central Anatolia. During its evolution, this Quaternary volcano produced pyroclastic deposits and lava flows. The great majority of these products are calc-alkaline in character and they constitute Kocdag and Erciyes sequences by repeated activities. Alkaline activity is mainly observed in the first stages of Kocdag and approximately first-middle stages of Erciyes sequences. Generally, Kocdag and Erciyes stages terminate by pyroclastic activities. The composition of lavas ranges from basalt to rhyolite (48.4–70.5 wt.% SiO₂). Calc-alkaline rocks are represented mostly by andesites and dacites. Some compositional differences between alkaline basaltic, basaltic and andesitic rocks were found; while the composition of dacites remain unchanged. All these volcanics are generally enriched in LIL and HFS elements relative to the orogenic values except Rb, Ba, Nb depleted alkaline basalt. ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd isotopic composition of the volcanics range between 0.703344–0.703964, 0.512920–0.512780 for alkaline basalts and change between 0.704322–0.705088, 0.512731–0.512630 for alkaline basaltic rocks whereas calc-alkaline rocks have relatively high Sr and Nd isotopic ratios (0.703434–0.705468, 0.512942–0.512600). Low Rb, Ba, Nb content with high Zr/Nb, low Ba/Nb, La/Yb ratio and low Sr isotopic composition suggest an depleted source component, while high Ba, Rb, Nb content with high La/Yb, Ba/Nb, low Zr/Nb and low ⁸⁷Sr/⁸⁶Sr ratios indicate an OIB-like mantle source for the generation of Erciyes alkaline magma. These elemental and ratio variations also indicate that the different mantle sources have undergone different degree of partial melting episodes. The depletion in Ba, Rb, Nb content may be explained by the removal of these elements from the source by slab-derived fluids which were released from pre-collisional subduction, modified the asthenospheric mantle. The chemically different mantle sources interacted with crustal materials to produce calc-alkaline magma. The Ba/Nb increase of calc-alkaline samples indicates the increasing input of crustal components to Erciyes volcanics. Sr and Nd isotopic compositions and elevated LIL and HFS element content imply that calc-alkaline magma may be derived from mixing of an OIB-like mantle melts with a subduction-modified asthenospheric mantle and involvement of crustal materials in intraplate environments.     

CO2- and LREE-rich mantle below eastern Australia: a REE and isotopic study of alkaline magmas and apatite-rich mantle xenoliths from the Southern Highlands Province,Australia

Alkaline magmatism in the Southern Highlands Province, New South Wales, Australia is associated with continental rifting. Near-primary liquids have a wide range in Nd and Sr isotope composition that indicates gross isotopic and chemical heterogeneities in a mantle source region depleted in light rare earth elements (LREE) for much of Earth's history. The large-ion lithophile element and LREE-enriched nature of the primary lavas ((Ce)_N = 95–182 and (Yb)_N = 8.5–13.3) is consistent with an enriched mantle source region. This elemental enrichment may be accomplished by veining of the subcontinental mantle with volatile-rich phases like amphibole, apatite and carbonate which provide the volatile flux necessary to trigger anatexis.Degassing of mantle CO₂ has led to migration of LREE-enriched fluids and local transformation of the lherzolitic mantle to pyroxenite veined by apatite ± kaersutite ± mica ± diopside. The mantle veining event may be related to upwelling of silica-undersaturated incompatible element-enriched magmas similar to the host magma of the Kiama xenoliths. In a relatively short period of time (100 m.y.), the Sr and Nd isotopes in essentially LREE-depleted mantle have evolved in response to low Sm/Nd and low Rb/Sr ratios, and now define a near-vertical vector on a isotope-isotope plot. From this rather unique signature we can infer that CO₂- and LREE-rich, Rb-poor mantle is a potentially suitable mantle source region for the genesis of alkali-potassic volcanic rocks characterized by a narrow range in⁸⁷Sr/⁸⁶Sr ratio and a wide range in¹⁴³Nd/¹⁴⁴Nd ratio (e.g. Leucite Hills).     

Origin of basalts from the Marquesas Archipelago (south central Pacific Ocean): isotope and trace element constraints

Basalts from the Marquesas Archipelago display significant variations according to magmatic type in ¹⁴³Nd/¹⁴⁴Nd (0.512710–0.512925) and ⁸⁷Sr/⁸⁶Sr (0.70288–0.70561) suggesting heterogeneities at various scales in the mantle source, with respectively the highest and lowest values in tholeiites compared to alkali basalts. This relationship is the reverse from that observed in the Hawaiian islands. Systematic indications of magma mixing are recognized from the relationships between trace element and isotopic ratios. Tholeiites from Ua Pou Island which have unradiogenic Sr (about 0.7028) plot close to basalts from Tubuai and St. Helena, i.e. distinctly below the main mantle trend in the Nd vs. Sr isotopic diagram. It is suggested that the source of these tholeiites is ancient subducted lithosphere which has suffered previous extraction of liquid with island arc tholeiite composition. The trace element and isotopic data of the basalts from the other Marquesas Islands imply the contamination of an equivalent source by an enriched component. This latter has trace element characteristics of the upper crust.     

Volcanism in the Sumisu Rift, I. Major element, volatile, and stable isotope geochemistry

A bimodal volcanic suite with KAr ages of 0.05–1.40 Ma was collected from the Sumisu Rift using alvin. These rocks are contemporaneous with island arc tholeiite lavas of the Izu-Ogasawara arc 20 km to the east, and provide a present day example of volcanism associated with arc rifting and back-arc basin initiation. Major element geochemistry of the basalts is most similar to that of basalts found in other, more mature back-arc basins, which indicates that back-arc basins need not begin their magmatic evolution with lavas bearing strong arc signatures.Volatile concentrations distinguish Sumisu Rift basalts from island arc basalts and MORB. H₂O contents, which are at least four times greater than in MORB, suppress plagioclase crystallization. This suppression results in a more mafic fractionating assemblage, which prevents Al₂O₃ depletion and delays the initiation of Fe₂O_3^(tot) and TiO₂ enrichment. However, unlike arc basalts,Fe^3+/ΣFe ratios are only slightly higher than in MORB and are insufficient to cause magnetite saturation early enough to suppress Fe₂O_3^(tot) and TiO₂ enrichment. Thus, major element trends are more similar to those of MORB than arcs.H₂O, CO₂ and S are undersaturated relative to pure phase solubility curves, indicating exsolution of an H₂O-rich mixed gas phase. HighH₂O/S, highδD, and low (MORB-like)δ³⁴S ratios are considered primary and distinctive of the back-arc basin setting.     

The Hasan Dagi stratovolcano (Central Anatolia, Turkey): evolution from calc-alkaline to alkaline magmatism in a collision zone

The Hasan Dagi volcano is one of the two large Plio-Quaternary volcanoes in Cappadocia (Central Anatolia, Turkey). Three stages of edifice construction have been identified for this volcano: Paleovolcano, Mesovolcano and Neovolcano. Most samples from Hasan Dagi volcano are calc-alkaline and define an almost complete trend from basaltic andesite to rhyolite. However, the more recent (Neovolcano) mafic samples are alkaline basalts. The mineralogical and geochemical characteristics of the oldest lavas (Keçikalesi (13 Ma) and Paleo-Hasan Dagi (7 Ma)) are significantly different from those of the younger lavas (Meso- and Neo-Hasan Dagi (<1 Ma)). Calcic plagioclase and pigeonite are typically observed in these older lavas. The Paleovolcano basalts are depleted in alkalis and display a tholeiitic tendency whereas the differentiated lavas are depleted in Na₂O but enriched in K₂O compared to younger lavas. There is an evolution through time towards higher TiO₂, Fe₂O₃^*, MgO, Na₂O and K₂O and lower Al₂O₃ and SiO₂ which is reflected in the basalt compositions. All the basalts display multi-element patterns typical of continental margin magmas with a significant enrichment in LILE (K, Rb, Ba and Th) and LREE and strong (Paleovolcano) to moderate (Meso- and Neovolcano) negative Nb, Zr and Ti anomalies. However, the younger basalts are the most enriched in incompatible elements, in agreement with their alkaline affinities and do not systematically display negative HFSE anomalies. REE data suggest an hydrous amphibole-bearing crystallization history for both Meso- and Neovolcano lavas. The distinction between the older and younger lavas is also apparent in trace element ratios such as Nb/Y, Ti/Y and Th/Y. These ratios indicate the role of a subducted component±crustal contamination in the genesis of the Hasan Dagi lavas, particularly for the oldest lavas (Keçikalesi and Paleo-Hasan Dagi). The decreasing influence of this component through time, over the last 6–7 m.y., has been accompanied by an increasing contribution of melt-enriched lithosphere. Although the range of variation of Sr, Nd and Pb isotopic ratios is small (0.70457–0.70515; 0.51262–0.51273; 18.80–18.94; 15.64–15.69; 38.87–39.10), it also reflects the evolution of the magma sources through time. Indeed, the youngest (Neovolcano) and most primitive basalts display significantly lower ⁸⁷Sr/⁸⁶Sr than the Paleo- and Mesovolcano basalts, whereas the Mesovolcano basalts display more radiogenic Pb than Paleovolcano samples. Magma mixing processes between initially heterogeneous and/or variably contaminated magmas may account for the genesis of the less differentiated and intermediate lavas (48–57% SiO₂). Meso- and Neovolcano differentiated lavas (60–68% SiO₂) are either derived from the analyzed basalts or from more primitive and more depleted magmas by fractional crystallization±some crustal contamination (AFC). Furthermore, the highly differentiated samples (72–75% SiO₂) are not strongly contaminated. The strong calc-alkaline character of Hasan Dagi lavas, in the absence of contemporaneous subduction, must reflect the heritage of the early subduction of the Afro–Arabian plate under the Eurasian plate. The evolution towards alkaline compositions through time is clearly related to the development of extensional tectonics in Central Anatolia in the Late Miocene.     

Petrological notes on the 1983 lavas at Mount Etna,Sicily, with reference to their REE and Sr—Nd isotope composition

The 1983 hawaiite of Mount Etna was sampled and analyzed for groundmass and mineral compositions, rare-earth-element concentrations and Sr-Nd isotope ratios.Microprobe data for coexisting mineral phases and glass show crystallization temperatures of around 1100° C from a rather differentiated hawaiite magma at rather highfO₂ (10^–8 at 1100° C), well above the QFM buffer.The hawaiites are characterized by a marked enrichment in the light REE similar to other alkaline magmas: the (Ce)_N/(Yb)_N is greater than 10, a feature these hawaiites have in common with alkaline magmas erupted earlier on Mount Etna. Since the Ce/Yb ratio cannot be affected by fractionation of clinopyroxene and plagioclase, it is taken as an accurate reflection of the LREE-enriched nature of the hawaiites. From this point of view, the Etnean hawaiites are identical to within-plate alkaline magmas erupted on the Hawaiian islands.This similarity extends to the Nd-Sr isotope features. Two hawaiites have⁸⁷Sr/⁸⁶Sr=0.70346 and 0.70352 and¹⁴³Nd/¹⁴⁴Nd=0.51286 and 0.51284. These data indicate a source similar to oceanic-island basalts, a source depleted in Rb/Sr and Nd/Sm for some period of time. The Sr isotope data are identical to that previously reported for Mount Etna.Extraction of hawaiites from depleted source regions requires either recent enrichment events, mixing of asthenospheric and lithospheric melts, or variable degrees of melting. At present, the data do not allow a clear decision.The peculiar tectonic setting of Mount Etna, between the relatively undeformed African foreland and the active Aeolian volcanic islands, may suggest contributions to the source region from subduction and within-plate processes. Etnean lavas have a geochemical imprint of subduction-related enrichment processes, and they also share petrological and chemical features identical to oceanic-island basalts whose source region has been affected by within-palte enrichment processes.Paper read at the IAVCEI Scientific Assembly, Giardini Naxos, September 16–21, 1985     

An estimate of the Nd isotopic composition of Iapetus seawater from ca. 490 Ma metalliferous sediments

Well-preserved metalliferous sediments and pillow basalts of Lower Ordovician age (ca. 490 Ma) have been studied in an attempt to specify the Nd isotopic composition of Iapetus seawater. Initial¹⁴³Nd/¹⁴⁴Nd ratios of the pillow basalts are indistinguishable from published initial ratios for the 505-Ma Bay of Islands ophiolite complex and are within the anticipated range for MORB-type basalts 500 Ma ago. Metalliferous sediments occur both interstitial to basalt pillows and as well-developed sedimentary accumulations. The initial¹⁴³Nd/¹⁴⁴Nd ratios for the non-interstitial variety range from 0.511851 to 0.511712 (ε_Nd = ?2.7to?5.4) and are considered to provide an estimate of¹⁴³Nd/¹⁴⁴Nd in Iapetus seawater. The interstitial metalliferous sediments show evidence for a significant basalt-derived Nd component. Although volcanic activity occurred at the margin of Iapetus essentially contemporaneous with the formation of the metalliferous sediments, it is clear that arc-type volcanic material was not a major source of Nd in Iapetus seawater. Rather the source of Nd was from continental regions with a similar average age to those supplying material to the present-day Atlantic Ocean.     

Isotope characteristics of submarine lavas from the Philippine Sea: implications for the origin of arc and basin magmas of the Philippine tectonic plate

Igneous rocks from the Philippine tectonic plate recovered on Deep Sea Drilling Project Legs 31, 58 and 59 have been analyzed for Sr, Nd and Pb isotope ratios. Samples include rocks from the West Philippine Basin, Daito Basin and Benham Rise (40–60 m.y.), the Palau-Kyushu Ridge (29–44 m.y.) and the Parece Vela and Shikoku basins (17–30 m.y.). Samples from the West Philippine, Parece Vela and Shikoku basins are MORB (mid-ocean ridge basalt)-like with ⁸⁷Sr/⁸⁶Sr= 0.7026−0.7032, ¹⁴³Nd/¹⁴⁴Nd= 0.51300−0.51315, and ²⁰⁶Pb/²⁰⁴Pb= 17.8−18.1. Samples from the Daito Basin and Benham Rise are OIB (oceanic island basalt)-like with ⁸⁷Sr/⁸⁶Sr= 0.7038−0.7040, ¹⁴³Nd/¹⁴⁴Nd= 0.51285−0.51291 and ²⁰⁶Pb/²⁰⁴Pb= 18.8−19.2. All of these rocks have elevated ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb compared to the Northern Hemisphere Regression Line (NHRL) and have δ²⁰⁷Pb values of 0 to +6 and δ²⁰⁸Pb values of +32 to +65. Lavas from the Palau-Kyushu Ridge, a remnant island arc, have ⁸⁷Sr/⁸⁶Sr= 7032−0.7035, ¹⁴³Nd/¹⁴⁴Nd= 0.51308−0.51310 and ²⁰⁶Pb/²⁰⁴Pb= 18.4−18.5. Unlike the basin magmas erupted before and after them, these lavas plot along the NHRL and have Pb-isotope ratios similar to modern Pacific plate MORB's. This characteristic is shared by other Palau-Kyushu Arc volcanic rocks that have been sampled from submerged and subaerial portions of the Mariana fore-arc.At least four geochemically distinct magma sources are required for these Philippine plate magmas. The basin magmas tap Source 1, a MORB-mantle source that was contaminated by EMI (enriched mantle component 1 [31]) and Source 2, an OIB-like mantle source with some characteristics of EMII (enriched mantle component 2 [31]). The arc lavas are derived from Source 3, a MORB-source or residue mantle including Sr and Pb from the subducted oceanic crust, and Source 4, MORB-source or residue mantle including a component with characteristics of HIMU (mantle component with high U/Pb [31]). These same sources can account for many of the isotopic characteristics of recent Philippine plate arc and basin lavas. The enriched components in these sources which are associated with the DUPAL anomaly were probably introduced into the asthenosphere from the deep mantle when the Philippine plate was located in the Southern Hemisphere 60 m.y.b.p.     

The relationship between calc-alkaline volcanism and within-plate continental rift volcanism: evidence from Scottish Palaeozoic lavas

Lower Carboniferous lavas from the Midland Valley and adjacent regions of Scotland are mildly alkaline and intraplate in nature. The sequence is dominated by basalt and hawaiite, although mugearite, benmoreite, trachyte and rhyolite are also present. Basic volcanic rocks display the LIL element and LREE enrichment typical of intraplate alkali basalt terrains. Low initial⁸⁷Sr/⁸⁶Sr (0.7029–0.7046), high ε_Nd (−0.4 to +5.6) and moderately radiogenic²⁰⁶Pb/²⁰⁴Pb (17.77–18.89) ratios are also comparable with alkali basalts from other continental rifts and oceanic islands.When the Carboniferous lavas are compared with subduction-related lavas of Old Red Sandstone age, erupted in and around the Midland Valley ca. 50 Ma earlier (at 410 Ma) remarkable similarities are apparent. Significant overlap occurs in Nd and Pb isotopic compositions. Sr isotopic compositions are, however, more radiogenic in the older subduction-related lavas. This, combined with high K and Rb concentrations in ORS lavas may be explained by the incorporation of a sediment component derived from the subducted slab, which by Lower Carboniferous times had been lost from the mantle source region by convection. A pronounced negative Nb anomaly in the ORS subduction-related lavas may be explained by the retention of a Nb-bearing phase in the mantle during hydrous melting of the mantle wedge above the subduction zone.Allowing for the effects of the added component from the subducted slab, there appears to be no necessity to invoke separate mantle source regions for the two suites of lavas: both may have been derived from chemically similar portions of mantle. If volcanic arc lavas are derived from the mantle wedge, the implication is that such a source lies at relatively shallow depth within the upper mantle: the same may therefore apply to the Carboniferous continental rift basalts. This evidence, combined with the fact that there is no evident hot-spot trail across the Midland Valley despite a long period of within-plate volcanism and rapid plate movements during the Carboniferous, suggests that the alkali basalt magmatism is not the product of a deep-seated mantle plume. Rather, the volcanism appears to owe more to passive rifting and to diapiric upwelling from a source region within the uppermost mantle.     

Early Paleozoic subduction of the Paleo-Asian Ocean: Geochronological and geochemical evidence from the Dashizhai basalts,Inner Mongolia

Zircon U-Pb results of basalt from the Dashizhai Town in Inner Mongolia, NE China, shows that the basaltic lava was erupted at 439±3 Ma, much older than the “Permian basalts” as previously thought. These rocks show arc-type trace element patterns (i.e., Nb-Ta depletion and light REE and large ion lithophile element enrichment) and unradiogenic Sr and highly radiogenic Nd and Hf isotope compositions. They can be subdivided into two petrogenetic groups: Group 1 basalts have relatively high TiO₂, MgO and compatible elements and low Sr and Th, characterized by mid-oceanic ridge basalt (MORB)-type Sr-Nd-Hf isotope compositions (⁸⁷Sr/⁸⁶Sr(i)=0.7028−0.7032, ε_Nd(t)=+9.8−+11.2, ε_Hf(t)=+16.1−+18.4). Group 2 has lower TiO₂, MgO and compatible elements and higher Sr and Th, and relatively evolved Sr-Nd-Hf isotope compositions (⁸⁷Sr/⁸⁶Sr(i)=0.7037−0.7038, ε_Nd(t)=+5.7−+7.3, ε_Hf(t)=+12.6−+13.0). Both groups were interpreted as melts derived from a metasomatized mantle wedge formed during the subduction of Paleo-Asian Ocean. The mantle source for Group 1 was probably a highly isotopically depleted oceanic mantle modified by predominant slab fluids; whereas subducted sediments had an important contribution to the melting source for Group 2. The petrogenesis of the Dashizhai basalts provides clear evidence for early Paleozoic subduction of the Paleo-Asian Ocean, and the highly radiogenic Nd and Hf compositions in these rocks suggest that these lavas and their possible intrusive counterparts were one of the important components for Phanerozoic crustal growth. Our and previous studies on the “Dashizhai Formation” volcanic rocks yield an unrealistic eruption range of 440-270 Ma for different rock types, we thus advise to disassemble the previously defined “Dashizhai Formation” into multiple lithologic units and to reinterpret the spatial and temporal distributions of different volcano-sedimentary associations. Supported by National Basic Research Program of China (Grant No. 2006CB403504)     

Petrological, geochemical and chronological constraints for the tectonic setting of the Dongco ophiolite in Tibet

The Dongco ophiolite occurred in the middle-western segment of the Bangong-Nujiang suture zone. The thickness of the ophiolite suite is more than 5 km, which is composed, from bottom to top, of the mantle peridotite, mafic-ultramafic cumulates, basic sills (dykes) and basic lava and tectoni- cally emplaced in Jurassic strata (Mugagongru Group). The Dongco cumulates consist of dunite- troctolite-olivine-gabbro, being a part of DTG series of mafic-ultramafic cumulates. The basic lavas are characterized by being rich in alkali (Na2O K2O), TiO2, P2O5 and a LREE-rich type pattern dip- ping right with [La/Yb]=6.94―16.6 as well as a trace elements spider-diagram with normal anomaly of Th, Nb, Ta, Hf. Therefore, the Dongco basic lavas belong to ocean-island basalt (OIB) and dis- tinctly differ from mid-ocean ridge basalt (MORB) and island-arc basalt (IAB) formed in the plate convergence margin. The basic lavas have higher 87Sr/86Sr (0.704363―0.705007), lower 143Nd/144Nd (0.512708―0.512887) and εNd(t ) from 2.7― 5.8, indicating that they derive from a two-components mixing mantle source of depleted mantle (DM) and enriched mantle (EMI). From above it is ready to see that the Dongco ophiolite forms in oceanic island (OIB) where the mantle source is replaced by a large amount of enriched material, therefore it distinctly differs from these ophiolites formed in island-arc and mid-oecan ridge. Newly obtained SHRIMP U-Pb dating for zircon of the cumulate troctolite is 132 ± 3 Ma and whole-rock dating of ~(39)Ar/~(40)Ar for the basalt is 173.4 ± 2.7 Ma and 140.9 ± 2.8 Ma, indicating that the Dongco ophiolite formed at Early Cretaceous and the middle-western segment of the Bangong-Nujiang oceanic basin was still in the developing and evolving period at Early Cretaceous.     

The Sm/Nd secular evolution of the continental crust and the depleted mantle

The published Nd isotopic data on rocks representative of either the continental crust or the depleted mantle are used to determine the Sm/Nd evolution of each system through time making allowance for a contribution from a primitive (chondritic) mantle. Screening using the ¹⁴⁷Sm/¹⁴⁴Nd ratio permits data of doubtful significance to be discarded. Mass balance equations describing mantle-crust exchange processes are numerically integrated. They suggest that crustal growth probably occurs through the addition of strongly LREE-enriched magmas derived from the mantle either directly (andesites) or indirectly (rhyolites). If the modern mean ¹⁴⁷Sm/¹⁴⁴Nd ratio of the crust is close to the sediment average (0.11), then progressive enrichment of LREE in the crust and depletion in the depleted mantle has occurred. If this ratio is of 0.13, then it, and the probable depleted-mantle ¹⁴⁷Sm/¹⁴⁴Nd ratio (0.26) have been constant over the last 3.8 Ga. The fraction of the total Nd (exclusive of the primitive mantle) stored in the continental crust has varied from 40% to 50% over the same period.The volume of the continents can have remained constant only if the rate of sediment reinjection into the mantle is 2.5 km³ a⁻¹ or more. For lower, probably more geologically reasonable, reinjection rates, a nearly uniform continent growth rate over the past 3.8 Ga is inferred. In all cases, the depleted mantle is continuously forming from a primitive reservoir.     

Characteristics of the mantle source region of sodium lamprophyres and petrogenetic tectonic setting in northeastern Hunan,China

~~Characteristics of the mantle source region of sodium lamprophyres and petrogenetic tectonic setting in northeastern Hunan,China~~     

Sr–Nd isotopic and chemical characteristics of the silicic magma reservoir of the Aira pyroclastic eruption, southern Kyushu, Japan

Sr and Nd isotope and geochemical investigations were performed on a remarkably homogeneous, high-silica rhyolite magma reservoir of the Aira pyroclastic eruption (22,000 years ago), southern Kyushu, Japan. The Aira caldera was formed by this eruption with four flow units (Osumi pumice fall, Tsumaya pryoclastic flow, Kamewarizaka breccia and Ito pyroclastic flow). Quite narrow chemical compositions (e.g., 74.0–76.5 wt% of SiO₂) and Sr and Nd isotopic values (⁸⁷Sr/⁸⁶Sr=0.70584–0.70599 and _Nd=−5.62 to −4.10) were detected for silicic pumices from the four units, with the exception of minor amounts of dark pumices in the units. The high Sr isotope ratios (0.7065–0.7076) for the dark pumices clearly suggest a different origin from the silicic pumices. Andesite to basalt lavas in pre-caldera (0.37–0.93 Ma) and post-caldera (historical) eruptions show lower ⁸⁷Sr/⁸⁶Sr (0.70465–0.70540) and higher _Nd (−1.03 to +0.96) values than those of the Aira silicic and dark pumices. Both andesites of pre- and post-caldera stages are very similar in major- and trace-element characteristics and isotope ratios, suggesting that the both andesites had a same source and experienced the same process of magma generation (magma mixing between basaltic and dacitic magmas). Elemental and isotopic signatures deny direct genetic relationships between the Aira pumices and pre- and post-caldera lavas. Relatively upper levels of crust (middle–upper crust) are assumed to have been involved for magma generation for the Aira silicic and dark pumices. The Aira silicic magma was derived by partial melting of a separate crust which had homogeneous chemistry and limited isotope compositions, while the magma for the Aira dark pumice was generated by AFC mixing process between the basement sedimentary rocks and basaltic parental magma, or by partial melting of crustal materials which underlay the basement sediments. The silicic magma did not occupy an upper part of a large magma body with strong compositional zonation, but formed an independent magma body within the crust. The input and mixing of the magma for dark pumices to the base of the Aira silicic magma reservoir might trigger the eruptions in the upper part of the magma body and could produce a slight Sr isotope gradient in the reservoir. An extremely high thermal structure within the crust, which was caused by the uprise and accumulation of the basaltic magma, is presumed to have formed the large volume of silicic magma of the Aira stage.     

Petrology of Peter I Øy (Peter I Island), West Antarctica

Peter I Øy is located in the Bellinghausen Sea, 400 km NE of Thurston Island, West Antarctica. It is a Pleistocene volcanic island situated adjacent to a former tranform fault on the continental rise of the presently passive margin between the Pacific and Antarctica. New K-Ar age determinations ranging from 0.1 to 0.35 Ma show that the volcanism responsible for this island took place at the same time as post-subduction, rift-related volcanism occurred in the nearby Marie Byrd Land and the Antarctic Peninsula. The rocks of the island are alkalic basalt and hawaiite, benmoreite and trachyte. The basic tocks typically contain phenocrysts of olivine (Fo_61–84), diopsidic augite, and plagioclase (ca. An₆₀). Small xenoliths are present and consist of mantle-type spinel lherzolite, cumulate clinopyroxenite and gabbro and felsic inclusions that consist of medium-grained strained quartz, plagioclase, and abundant colorless glass. Chemically, the basic rocks are characterized by rather high MgO (7.8–10.2 wt.%) and TiO₂ (3.1–3.7 wt.%) and relatively low CaO (8.4–9.5 wt.%) contents. They have steep REE patterns, [(La/Yb)_N = 20] with HREE only 5 x chrondrite. Y and Sc are almost constant at relatively low levels. Compatible trace elements such as Ni and Cr show considerable variation (190–300 and 150–470 ppm, respectively.), whereas V shows only little variation. Sr and Nd isotope ratios vary slightly with ⁸⁷Sr/⁸⁶Sr averaging 0.70388 and ¹⁴³Nd/¹⁴⁴Nd 0.512782, both typical for ocean island volcanism. Lead isotope ratios are consistently high in basalts; ²⁰⁶Pb/²⁰⁴Pb = 19.194, ²⁰⁷Pb/²⁰⁴Pb = 15.728 and ²⁰⁸Pb/²⁰⁴Pb = 39.290, whereas benmoreïte is somewhat less radiogenic. Oxygen isotope analyses average δ¹⁸O = +6.0‰. Incompatible trace elements vary by a factor of 1.5–2.0 within the range of the basic rocks. It is proposed that the incompatible trace-element variations represent different degrees (<10%) of partial melting, and that these melts were later modified by minor (<15‰) olivine and spinel fractionation. The very small variation in Y (and Sc) and the very fractionated REE pattern indicate that the source had an Y- and HREE-rich residual phase, most probably garnet. Furthermore, it is suggested that the source was slightly hydrous and that melting took place at 18–20 kbar. Trachyte was derived by multiphase fractionation of ne-normative basalts, and benmoreite from hy-normative parental liquids. The rocks of Peter I Øy are generally of the same type and age as those outcropping in extensional regimes on the nearby continent, and therefore, these occurrences may be related to each other in some way. However, the Peter I Øy rocks are considerably more radiogenic in strontium and less radiogenic in neodymium than the rocks of the Antarctic Peninsula and Marie Byrd Land. Possible explanations are that Peter I Øy represent asthenospheric hot spot activity, or transtensional rifting as subduction ceased.     

Lau Basin basalts (LBB): trace element and SrNd isotopic evidence for heterogeneity in backarc basin mantle

Diverse⁸⁷Sr/⁸⁶Sr and¹⁴³Nd/¹⁴⁴Nd isotopic compositions among basalts from the Lau Basin (LBB), an active backarc basin in the southwest Pacific, indicate heterogeneity in the underlying mantle. Isotopic compositions display bimodal distributions which are related to geographic location. Type I LBB (⁸⁷/Sr⁸⁶Sr 0.70366;¹⁴³Nd/¹⁴⁴Nd 0.51297) include tholeiites from the central basin, Peggy Ridge, and Rochambeau Bank, while Type II basaltic and andesitic glasses from the northeastern portion of the basin, near Niua Fo'ou island, have higher⁸⁷Sr/⁸⁶Sr ( 0.7038) and lower ¹⁴³Nd/¹⁴⁴Nd ( 0.51288). Both depleted (e.g. N-MORB) and enriched (e.g. E-MORB) trace element abundances occur among Type I and Type II LBB.Covariation between trace element and isotopic ratios among Type I LBB is consistent with mixing between depleted mantle similar to the source for MORB and relatively enriched peridotite similar to the source for E-MORB. Relative to MORB, uniformly high⁸⁷Sr/⁸⁶Sr ( +0.0005) among all Type I LBB for given Nd isotopic compositions ( ε_Nd = +8 to +12) may reflect a lithospheric component, such as ancient recycled altered ocean crust. Type II LBB have SrNd isotopic compositions which are gradational between enriched mantle similar to the source of OIB and a component with distinct Sr isotopic composition such as that observed in Samoan post-erosional basalts. Isotopic and geographic discontinuity between Type I and Type II LBB, and isotopic affinity of Type II and Niua Fo`ou island basalts with those from Samoa suggests that volcanism in the northeastern portion of the basin is tapping deeper mantle beneath the adjoining Pacific plate, as well as Indo-Australian mantle overlying the Pacific lithosphere that is subducted into the Tonga Trench.