Generation of Cenozoic intraplate basalts in the big mantle wedge under eastern Asia

The roles of subduction of the Pacific plate and the big mantle wedge (BMW) in the evolution of east Asian continental margin have attracted lots of attention in past years. This paper reviews recent progresses regarding the composition and chemical heterogeneity of the BMW beneath eastern Asia and geochemistry of Cenozoic basalts in the region, with attempts to put forward a general model accounting for the generation of intraplate magma in a BMW system. Some key points of this review are summarized in the following. (1) Cenozoic basalts from eastern China are interpreted as a mixture of high-Si melts and low-Si melts. Wherever they are from, northeast, north or south China, Cenozoic basalts share a common low-Si basalt endmember, which is characterized by high alkali, Fe₂O₃^T and TiO₂ contents, HIMU-like trace element composition and relatively low ²⁰⁶Pb/²⁰⁴Pb compared to classic HIMU basalts. Their Nd-Hf isotopic compositions resemble that of Pacific Mantle domain and their source is composed of carbonated eclogites and peridotites. The high-Si basalt endmember is characterized by low alkali, Fe₂O ₃ ^T and TiO₂ contents, Indian Mantle-type Pb-Nd-Hf isotopic compositions, and a predominant garnet pyroxenitic source. High-Si basalts show isotopic provinciality, with those from North China and South China displaying EM1-type and EM2-type components, respectively, while basalts from Northeast China containing both EM1- and EM2-type components. (2) The source of Cenozoic basalts from eastern China contains abundant recycled materials, including oceanic crust and lithospheric mantle components as well as carbonate sediments and water. According to their spatial distribution and deep seismic tomography, it is inferred that the recycled components are mostly from stagnant slabs in the mantle transition zone, whereas EM1 and EM2 components are from the shallow mantle. (3) Comparison of solidi of garnet pyroxenite, carbonated eclogite and peridotite with regional geotherm constrains the initial melting depth of high-Si and low-Si basalts at <100 km and ～300 km, respectively. It is suggested that the BMW under eastern Asia is vertically heterogeneous, with the upper part containing EM1 and EM2 components and isotopically resembling the Indian mantle domain, whereas the lower part containing components derived from the Pacific mantle domain. Contents of H₂O and CO₂ decrease gradually from bottom to top of the BMW. (4) Melting of the BMW to generate Cenozoic intraplate basalts is triggered by decarbonization and dehydration of the slabs stagnated in the mantle transition zone.     

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.     

The geochemistry of oceanic basalts in the vicinity of transform faults: Observations and implications

Consideration of geochemical data from basalts formed near major Atlantic and Pacific transform faults reveals two significant sets of observations. First, compared to basalts formed far from the transform, basalts near the ridge/transform intersection have, for the same MgO contents, higher abundances of TiO₂ and other incompatible elements, higher La/Sm and La/Yb ratios, and often higher FeO. These enrichments are distinct from and occur in addition to the more variable and fractionated compositions which have been frequently noted [10–13]. Modeling of this “transform fault effect” using data from the Tamayo/EPR intersection suggests the chemical systematics are caused by decreasing extents of melting as the transform is approached.Second, there are chemical discontinuities in the major element, trace element and isotopic chemistry of basalts across many transforms. These “transform discontinuities” occur in normal ocean crust as well as around hot spots.Consideration of the melting zone in the mantle suggests that the transform fault effect is a natural consequence of the ridge/transform plate boundary. The melting zone beneath a ridge segment must terminate across the transform, leading to lower extents of melting at the transform edge. The surface manifestation of the change in the melting zone may be affected by the age of the transform offset, the spreading rate, the transform spacing and the interaction of mantle flow with the local thermal structure; it may be obscured by episodic magma chamber processes and mantle heterogeneity.The significance of transform discontinuities depends on whether they persist with age. If they do not, then temporally variable crust-forming processes may produce changes along a flow line similar to those at zero age across a transform. If, on the other hand, a discontinuity persists with age, then the transform may be related to a fundamental discontinuity in the underlying mantle. Long-lived transform discontinuities would have profound implications for the nature of plate motions, mantle convection and mantle heterogeneity.     

Chlorine in submarine glasses from the Lau Basin: seawater contamination and constraints on the composition of slab-derived fluids

Measurements of chlorine concentrations in matrix glasses from 18 primitive (>6 wt% MgO) and eight evolved lavas from active spreading centers in the Lau Basin back-arc system provide insight into the processes which control chlorine concentrations in subduction-related magmas, and can be used to investigate chlorine enrichment related to fluids derived from the underlying subducted slab. Chlorine contents of the glasses are highly variable (0.008-0.835 wt%) and generally high with respect to uncontaminated mid-ocean ridge basalt. Chlorine contents are highest in fractionated lavas from propagating ridge tips and lowest in more primitive basaltic lavas. Two different styles of enrichment in chlorine (relative to other incompatible elements) are recognized. Glasses from the Central Lau Spreading and Eastern Lau Spreading Center typically have low Ba/Nb ratios indicating minimal input of slab-derived components, and high to very high ratios of chlorine relative to K₂O, H₂O, and TiO₂. This style of chlorine enrichment is highest in the most fractionated samples and is consistent with crustal assimilation of chlorine-rich altered ocean crust material. Data from the literature suggest that contamination by chlorine-rich seawater-derived components also characterizes the Woodlark Basin and North Fiji Basin back-arc systems. The second style of chlorine enrichment reflects input from slab-derived fluid(s) to the mantle wedge from the adjacent Tonga subduction zone. Basaltic glasses from the Valu Fa Ridge and Mangatolu Triple Junction show correlations between ratios of chlorine and K₂O, H₂O, and TiO₂ and indices of slab-derived fluid input such as Ba/Nb, Ba/Th and U/Th, consistent with chlorine in these lavas originating from a saline fluid added to the mantle wedge. Within the Valu Fa Ridge the measured range of chlorine contents equates to a chlorine flux of 224-1120 kg/m/yr to the back-arc crust. Using a simple melting model and additional data from other back-arc and arc sample suites we conclude that chlorine is a major component within the slab fluids that contribute to many arc and back-arc melting systems, and probably plays an important role in regulating trace element transport by slab fluids in the mantle wedge. For the back-arc suites we have examined the estimated Cl/H₂O and Cl/K₂O ratios in the slab fluid component correlate with proximity to the arc front, suggesting that progressive dehydration of the slab and/or re-equilibration and transport within the mantle wedge may influence the overall degree of chlorine enrichment within the slab fluid component. The degree of chlorine enrichment observed in most back-arc lavas also appears too great to be explained solely by melting of amphibole, phlogopite or apatite within the mantle source and suggests that chlorine must be present in another phase, possibly a chlorine-rich fluid.     

Geochemistry of basalts from the Dumisseau Formation, southern Haiti: implications for the origin of the Caribbean Sea crust

Basalt and diabase from the Cretaceous Dumisseau Formation, southern Haiti have Mg-numbers of 43–63, TiO₂ contents of 1.6–3.9% and La abundances of 3.6–15.3 ppm.La/Ta ratios average 10, and indicate that the basalts are oceanic in character, distinct from the arc associations forming the northern part of Haiti. Oldest lavas have low TiO₂ (1.6%) and are LREE-depleted, similar to N-MORBs, whereas overlying lavas have higher TiO₂ (2–3.9%) and are LREE-enriched, similar to E-MORBs or hotspot basalts.⁸⁷Sr⁸⁶Sr ratios vary from 0.70280 to 0.70316,¹⁴³Nd¹⁴⁴Nd from 0.512929 to 0.513121, and²⁰⁶Pb²⁰⁴Pb from 19.00 to 19.27. LREE-depleted lavas have high¹⁴³Nd¹⁴⁴Nd (0.51309–0.51310) typical of MORBs, whereas¹⁴³Nd¹⁴⁴Nd in the LREE-enriched lavas varies widely (0.512929–0.513121).Chemical features of the Dumisseau basalts are equivalent to those of Caribbean seafloor basalts recovered on DSDP Leg 15, and support the contention that the Dumisseau is an uplifted section of Caribbean Sea crust. Oldest lavas are analogous to MORB-like basalts cored at Leg 15 Sites 146, 150, 152 and 153, and the overlying lavas are analogous to incompatible-element-enriched basalts cored at Site 151 on the Beata Ridge. Isotopic compositions of the Dumisseau basalts overlap with those of the eastern Pacific Galapagos and Easter Island hotspots. However, the presence of N-MORB basalts in the lower part of the Dumisseau and at the majority of Leg 15 Sites indicates that the anomalously thick Caribbean crust probably did not originate as a hotspot-related basaltic plateau, but may have been generated by on-ridge or near-ridge hotspot magmatism.     

Spinels in Mid-Atlantic Ridge basalts: Chemistry and occurrence

Three groups of spinels have been identified in dredged basalts from the Mid-Atlantic Ridge in the Azores region (30–40°N): (1) magnesiochromites with 0.4–0.5 Cr/(Cr + Al) are most common and characteristic of olivine tholeiites of the region; (2) titaniferous magnesiochromites are found in an olivine basalt with alkali affinities, of local occurrence and evolved in relatively high fugacity of oxygen; (3) chromian spinels with 0.23 Cr/(Cr + Al) occur in unusual high-Al picrites of local occurrence and possible high-pressure origin. Spinels are restricted in occurrence to the least fractionated lavas, with FeO^*/FeO^* + MgO ratio less than 0.575 and with Cr content greater than 350 ppm. A close relationship between Al content of liquidus spinel and Al content of magma has been observed for basaltic types. High-Al spinels deviating from this relationship, such as those found in picritic lavas from the Mid-Atlantic Ridge, may have crystallized at high pressure. The use of spinels as geobarometers in magmas of a restricted compositional range seems a promising prospect. There is no evidence of systematic variation in spinel chemistry of occurrence along the Mid-Atlantic Ridge, such as could be related to different mantle sources of the basalts, plume versus non-plume or binary mantle mixing.     

Geochemistry of rare earth elements in basalts from the Walvis Ridge: implications for its origin and evolution

Selected basalts from a suite of dredged and drilled samples (IPOD sites 525, 527, 528 and 530) from the Walvis Ridge have been analysed to determine their rare earth element (REE) contents in order to investigate the origin and evolution of this major structural feature in the South Atlantic Ocean. All of the samples show a high degree of light rare earth element (LREE) enrichment, quite unlike the flat or depleted patterns normally observed for normal mid-ocean ridge basalts (MORBs). Basalts from Sites 527, 528 and 530 show REE patterns characterised by an arcuate shape and relatively low (Ce/Yb)_N ratios (1.46–5.22), and the ratios show a positive linear relationship to Nb content. A different trend is exhibited by the dredged basalts and the basalts from Site 525, and their REE patterns have a fairly constant slope, and higher (Ce/Yb)_N ratios (4.31–8.50).These differences are further reflected in the ratios of incompatible trace elements, which also indicate considerable variations within the groups. Mixing hyperbolae for these ratios suggest that simple magma mixing between a “hot spot” type of magma, similar to present-day volcanics of Tristan da Cunha, and a depleted source, possibly similar to that for magmas being erupted at the Mid-Atlantic Ridge, was an important process in the origin of parts of the Walvis Ridge, as exemplified by Sites 527, 528 and 530. Site 525 and dredged basalts cannot be explained by this mixing process, and their incompatible element ratios suggest either a mantle source of a different composition or some complexity to the mixing process. In addition, the occurrence of different types of basalt at the same location suggests there is vertical zonation within the volcanic pile, with the later erupted basalts becoming more alkaline and more enriched in incompatible elements.The model proposed for the origin and evolution of the Walvis Ridge involves an initial stage of eruption in which the magma was essentially a mixture of enriched and depleted end-member sources, with the N-MORB component being small. The dredged basalts and Site 525, which represent either later-stage eruptives or those close to the hot spot plume, probably result from mixing of the enriched mantle source with variable amounts and variable low degrees of partial melting of the depleted mantle source. As the volcano leaves the hot spot, these late-stage eruptives continue for some time. The change from tholeiitic to alkalic volcanism is probably related either to evolution in the plumbing system and magma chamber of the individual volcano, or to changes in the depth of origin of the enriched mantle source melt, similar to processes in Hawaiian volcanoes.     

Identification of recycled continental material in the mantle from Sr,Nd and Pb isotope investigations

Pb, Nd and Sr isotope compositions of oceanic basalts have been used to identify recycled components of continent derivation in the mantle. The isotopic compositions of Sr, Nd and Pb, together with U, Pb, Sm, Nd, Rb, and Sr abundances have been determined for back-arc basalt glasses from the Scotia Sea and Parece Vela and West Philippine Basins, in addition to basalts from South Sandwich Islands, Ascension, St. Helena and Tristan da Cunha. Comparisons made between the isotopic compositions of South Sandwich Islands basalts and Atlantic MORB glasses permit the identification of recycled components of continent derivation in the source of the island arc basalts. Recycled Sr of continent derivation is also recognisable in back-arc basalt glasses from the Scotia Sea and Parece Vela and West Philippine Basins. However, contemporary reinjection of material with the isotopic structures similar to those identified as a component of island arc and back-arc regions cannot be the sole or dominant influence on the fine structure observed in MORB glasses from the Atlantic Ocean, nor the isotopic compositions of Tristan da Cunha, St. Helena and Ascension basalts. Recycled materials are likely to have been responsible for the generation of these heterogeneities only if they have been stored in the mantle for periods of time exceeding 10⁹ years.     

Anomalously nucleogenic neon in North Chile Ridge basalt glasses suggesting a previously degassed mantle source

Fresh basalt glasses from the North Chile Ridge (NCR) in the southeastern Pacific have Ne isotopic compositions distinctly different from typical mid-ocean ridge basalts (MORB). In a three-isotope plot of ²⁰Ne/²²Ne vs. ²¹Ne/²²Ne, the NCR data define a correlation line with a slope smaller than that of the MORB correlation line, i.e. their Ne composition is more nucleogenic than that of MORB. ³He/⁴He ratios are slightly lower than the MORB average, whereas in a few stepwise heating fractions very high ⁴⁰Ar/³⁶Ar ratios up to 28,000 are found. One model to explain the data assumes contamination of the NCR mantle source by material from the continental or oceanic crust, but in addition to difficulties with quantitatively reconciling the noble gas patterns with such a model it seems unable to account for some geochemical characteristics of NCR basalts reported earlier [Bach et al., Earth Planet. Sci. Lett. 142 (1996) 223–240], such as depletions in highly incompatible elements and unradiogenic Sr isotope compositions. Therefore we favor the scenario of a mantle source which was depleted and degassed previously, possibly as a residue from mantle melting beneath the southern East Pacific Rise that was transported to the NCR and melted again. The time during which such a depleted reservoir would have to be separated from the MORB mantle is estimated at 10–100 Ma based on U/Th–Ne systematics, in reasonable agreement with the time scale deduced from the formation history of the NCR and the temporal evolution of the southeast Pacific.     

Geochemistry of basalts drilled in the North Atlantic by IPOD Leg 49: Implications for mantle heterogeneity

IPOD Leg 49 recovered basalts from 9 holes at 7 sites along 3 transects across the Mid-Atlantic Ridge: 63°N (Reykjanes), 45°N and 36°N (FAMOUS area). This has provided further information on the nature of mantle heterogeneity in the North Atlantic by enabling studies to be made of the variation of basalt composition with depth and with time near critical areas (Iceland and the Azores) where deep mantle plumes are thought to exist. Over 150 samples have been analysed for up to 40 major and trace elements and the results used to place constraints on the petrogenesis of the erupted basalts and hence on the geochemical nature of their source regions.It is apparent that few of the recovered basalts have the geochemical characteristics of typical “depleted” midocean ridge basalts (MORB). An unusually wide range of basalt compositions may be erupted at a single site: the range of rare earth patterns within the short section cored at Site 413, for instance, encompasses the total variation of REE patterns previously reported from the FAMOUS area. Nevertheless it is possible to account for most of the compositional variation at a single site by partial melting processes (including dynamic melting) and fractional crystallization. Partial melting mechanisms seem to be the dominant processes relating basalt compositions, particularly at 36°N and 45°N, suggesting that long-lived sub-axial magma chambers may not be a consistent feature of the slow-spreading Mid-Atlantic Ridge.Comparisons of basalts erupted at the same ridge segment for periods of the order of 35 m.y. (now lying along the same mantle flow line) do show some significant inter-site differences in Rb/Sr, Ce/Yb,⁸⁷Sr/⁸⁶Sr, etc., which cannot be accounted for by fractionation mechanisms and which must reflect heterogeneities in the mantle source. However when hygromagmatophile (HYG) trace element levels and ratios are considered, it is the constancy or consistency of these HYG ratios which is the more remarkable, implying that the mantle source feeding a particular ridge segment was uniform with respect to these elements for periods of the order of 35 m.y. and probably since the opening of the Atlantic. Yet these HYG element ratios at 63°N are very different from those at 45°N and 36°N and significantly different from the values at 22°N and in “MORB”.The observed variations are difficult to reconcile with current concepts of mantle plumes and binary mixing models. The mantle is certainly heterogeneous, but there is not simply an “enriched” and a “depleted” source, but rather a range of sources heterogeneous on different scales for different elements — to an extent and volume depending on previous depletion/enrichment events. HYG element ratios offer the best method of defining compositionally different mantle segments since they are little modified by the fractionation processes associated with basalt generation.     

Miocene to Late Quaternary Patagonian basalts (46–47°S): Geochronometric and geochemical evidence for slab tearing due to active spreading ridge subduction

Miocene to Quaternary large basaltic plateaus occur in the back-arc domain of the Andean chain in Patagonia. They are thought to result from the ascent of subslab asthenospheric magmas through slab windows generated from subducted segments of the South Chile Ridge (SCR). We have investigated three volcanic centres from the Lago General Carrera–Buenos Aires area (46–47°S) located above the inferred position of the slab window corresponding to a segment subducted 6 Ma ago. (1) The Quaternary Río Murta transitional basalts display major, trace elements, and Sr and Nd isotopic features similar to those of oceanic basalts from the SCR and from the Chile Triple Junction near Taitao Peninsula (e.g., (⁸⁷Sr/⁸⁶Sr)_o = 0.70396–0.70346 and εNd = + 5.5 − + 3.0). We consider them as derived from the melting of a Chile Ridge asthenospheric mantle source containing a weak subduction component. (2) The Plio-Quaternary (< 3.3 Ma) post-plateau basanites from Meseta del Lago Buenos Aires (MLBA), Argentina, likely derive from small degrees of melting of OIB-type mantle sources involving the subslab asthenosphere and the enriched subcontinental lithospheric mantle. (3) The main plateau basaltic volcanism in this region is represented by the 12.4–3.3-Ma-old MLBA basalts and the 8.2–4.4-Ma-old basalts from Meseta Chile Chico (MCC), Chile. Two groups can be distinguished among these main plateau basalts. The first group includes alkali basalts and trachybasalts displaying typical OIB signatures and thought to derive from predominantly asthenospheric mantle sources similar to those of the post-plateau MLBA basalts, but through slightly larger degrees of melting. The second one, although still dominantly alkalic, displays incompatible element signatures intermediate between those of OIB and arc magmas (e.g., La/Nb > 1 and TiO₂ < 2 wt.%). These intermediate basalts differ from their strictly alkalic equivalents by having lower High Field Strength Element (HFSE) and higher εNd (up to + 5.4). These features are consistent with their derivation from an enriched mantle source contaminated by ca. 10% rutile-bearing restite of altered oceanic crust. The petrogenesis of the studied Mio-Pliocene basalts from MLBA and MCC is consistent with contributions of the subslab asthenosphere, the South American subcontinental lithospheric mantle and the subducted Pacific oceanic crust to their sources. However, their chronology of emplacement is not consistent with an ascent through an asthenospheric window opened as a consequence of the subduction of segment SCR-1, which entered the trench at 6 Ma. Indeed, magmatic activity was already important between 12 and 8 Ma in MLBA and MCC as well as in southernmost plateaus, i.e., 6 Ma before the subduction of the SCR-1 segment. We propose a geodynamic model in which OIB and intermediate magmas derived from deep subslab asthenospheric mantle did uprise through a tear-in-the-slab, which formed when the southernmost segments of the SCR collided with the Chile Trench around 15 Ma. During their ascent, they interacted with the Patagonian supraslab mantle and, locally, with slivers of subducted Pacific oceanic crust that contributed to the geochemical signature of the intermediate basalts.     

Isotope and trace element geochemistry of young Pacific seamounts: implications for the scale of upper mantle heterogeneity

Basalts from young seamounts situated within 6.8 m.y. of the East Pacific Rise, between 9° and 14°N latitude, display significant variations in ¹⁴³Nd/¹⁴⁴Nd (0.51295–0.51321), ⁸⁷Sr/⁸⁶Sr (0.7025–0.7031), and(La/Sm)_N (0.415–3.270). Nd and Sr isotope ratios are anti-correlated and form a trend roughly parallel to the “mantle array” on a¹⁴³Nd/¹⁴⁴Nd vs.⁸⁷Sr/⁸⁶Sr variation diagram. Nd and Sr isotope ratios display negative and positive correlations, respectively, with(La/Sm)_N. The geochemical variations observed at the seamounts are nearly as great or greater than those observed over several hundred kilometers of the Reykjanes Ridge, or at the islands of Iceland or Hawaii.

Samples from one particular seamount, Seamount 6, display nearly the entire observed range of chemical variations, offering an ideal opportunity to constrain the nature of heterogeneities in the source mantle. Systematics indicative of magma mixing are recognized when major elements, trace elements, trace element ratios, and isotope ratios are compared with each other in all possible permutations. The source materials required to produce the end-member magmas are: (1) a typical MORB-source-depleted peridotite; and (2) a relatively enriched material which may represent ancient mantle segregations of basaltic melt, incompletely mixed remnants of subducted ocean crust, or metasomatized peridotite such as that found at St. Paul's Rocks or Zabargad Island. Due to the proximity of the seamounts to the East Pacific Rise (EPR), the source materials are thought to comprise an intimate mixture in the mantle immediately underlying the seamounts and the adjacent EPR. Lavas erupted at the ridge axis display a small range of isotopic and incompatible trace element compositions because the large degrees of melting and presence of magma chambers tend to average the chemical characteristics of large volumes of mantle.

If the postulated mantle materials, with large magnitude, small-scale heterogeneities, are ubiquitous in the upper mantle, chemical variations in basalts ranging from MOR tholeiites to island alkali basalts may reflect sampling differences rather than changes in bulk mantle chemistry.     

Origin of Icelandic basalts: A review of their petrology and geochemistry

The petrology and geochemistry of Icelandic basalts have been studied for more than a century. The results reveal that the Holocene basalts belong to three magma series: two sub-alkaline series (tholeiitic and transitional alkaline) and an alkali one. The alkali and the transitional basalts, which occupy the off-rift volcanic zones, are enriched in incompatible trace elements compared to the tholeiites, and have more radiogenic Sr, Pb and He isotope compositions. Compared to the tholeiites, they are most likely formed by partial melting of a lithologically heterogeneous mantle with higher proportions of melts derived from recycled oceanic crust in the form of garnet pyroxenites compared to the tholeiites. The tholeiitic basalts characterise the mid-Atlantic rift zone that transects the island, and their most enriched compositions and highest primordial (least radiogenic) He isotope signature are observed close to the centre of the presumed mantle plume. High-MgO basalts are found scattered along the rift zone and probably represent partial melting of refractory mantle already depleted of initial water-rich melts. Higher mantle temperature in the centre of the Iceland mantle plume explains the combination of higher magma productivity and diluted signatures of garnet pyroxenites in basalts from Central Iceland. A crustal component, derived from altered basalts, is evident in evolved tholeiites and indeed in most basalts; however, distinguishing between contamination by the present hydrothermally altered crust, and melting of recycled oceanic crust, remains non-trivial. Constraints from radiogenic isotope ratios suggest the presence of three principal mantle components beneath Iceland: a depleted upper mantle source, enriched mantle plume, and recycled oceanic crust.The study of glass inclusions in primitive phenocrysts is still in its infancy but already shows results unattainable by other methods. Such studies reveal the existence of mantle melts with highly variable compositions, such as calcium-rich melts and a low-¹⁸O mantle component, probably recycled oceanic crust. Future high-resolution seismic studies may help to identify and reveal the relative proportions of different lithologies in the mantle.     

Bimodal tholeiitic and mildly alkalic basalts from Bhir area,central Deccan Volcanic Province,India: Geochemistry and petrogenesis

Bimodal tholeiitic and mildly alkalic basalts occur near Bhir, in the central part of Deccan Volcanic Province (DVP). Major and trace element concentrations show that, of the ten flows, nine are tholeiitic and one is an alkalic basalt. The Bhir basalts have a wide range of chemical composition. Geochemical variations in the stratigraphic section define three distinct phases of evolution (zones 1 to 3). Crystal fractionation of plagioclase, clinopyroxene, olivine and Fe–Ti oxide expanded the compositional range. Low Mg#s (39–55), low concentrations of Ni and Cr and high Zr suggest the evolved nature of the Bhir basalts. Fractionation modeling suggests about 42% fractional crystallization.In spite of the dominant role of fractional crystallization in the evolution of Bhir basalts, some other processes must be sought to explain the chemical variations. Crustal contamination, magma mixing and degree of partial melting are suggested to explain the observed chemical variations. Resorption, reverse zoning and compositional bimodality in plagioclase phenocrysts indicate magma mixing. Samples of flows one and four suspected of being contaminated all have enriched SiO₂ and LILE (K, Rb, and Ba) contents and depletion in Ti and P, believed to be due to ‘granitic’ crustal contamination.As compared to tholeiitic basalts, the alkalic basalts are characterized by low SiO₂ and high TiO₂, Na₂O, K₂O and P₂O₅. Alkalic basalts are richer in LILE (Rb and Ba), HFSE (Nb, Zr, and Y) and REE than the tholeiitic basalts. The alkalic basalt occurrence is important from a petrogenetic point of view and also suggests that the sources of alkalic basalt magmas may be of variable ages under different parts of the DVP. Based on major, trace and rare earth element distributions it is suggested that asthenospheric mantle having affinities with the source of OIB was the source material of the magmas and the range in the composition of tholeiitic and alkalic basalts was probably controlled by different degrees of melting and/or inhomogeneities in the mantle source.     

The petrology, phase relations and tectonic setting of basalts from the taupo volcanic zone, New Zealand and the Kermadec Island arc - havre trough, SW Pacific

Volcanism in the Taupo Volcanic Zone (TVZ) and the Kermadec arc-Havre Trough (KAHT) is related to westward subduction of the Pacific Plate beneath the Indo-Australian Plate. The tectonic setting of the TVZ is continental whereas in KAHT it is oceanic and in these two settings the relative volumes of basalt differ markedly. In TVZ, basalts form a minor proportion (< 1%) of a dominant rhyolite (97%)-andesite association while in KAHT, basalts and basaltic andesites are the major rock types. Neither the convergence rate between the Pacific and Indo-Australian Plates nor the extension rates in the back-arc region or the dip of the Pacific Plate Wadati-Benioff zone differ appreciably between the oceanic and continental segments. The distance between the volcanic front and the axis of the back-arc basin decreases from the Kermadec arc to TVZ and the distance between trench and volcanic front increases from around 200 km in the Kermadec arc to 280 km in TVZ. These factors may prove significant in determining the extent to which arc and backarc volcanism in subduction settings are coupled.All basalts from the Kermadec arc are porphyritic (up to 60% phenocrysts) with assemblages generally dominated by plagioclase but with olivine, clinopyroxene and orthopyroxene. A single dredge sample from the Havre Trough back arc contains olivine and plagioclase microphenocrysts in glassy pillow rind and is mildly alkaline (< 1% normative nepheline) contrasting with the tholeiitic nature of the other basalts. Basalts from the TVZ contain phenocryst assemblages of olivine + plagioclase ± clinopyroxene; orthopyroxene phenocrysts occur only in the most evolved basalts and basaltic andesites from both TVZ and the Kermadec Arc.Sparsely porphyritic primitive compositions (Mg/(Mg+Fe²) > 70) are high in Al₂O₃ (>16.5%), and project in the olivine volume of the basalt tetrahedron. They contain olivine (Fo₈₇) phenocrysts and plagioclase (> An₆₀) microphenocrysts. These magmas have ratios of CaO/Al₂O₃, A1₂O₃/TiO₂ and CaO/TiO₂ in the range of MORB and MORB picrites and can evolve to the low-pressure MORB cotectic by crystallisation of olivine±plagiociase. Such rocks may be the parents of other magmas whose evolutionary pathways are complicated by interaction of crystal fractionation, crystal accumulation and mixing processes and the filtering action of crust of variable density and thickness. The interplay of these processes likely accounts for the scatter of data about the cotectic. More evolved rocks from both TVZ and KAHT contain clinopyroxene and orthopyroxene phenocrysts and their compositions merge with basaltic andesites and andesites. Stepwise least-squares modelling using phenocryst assemblages in proportions observed in the rocks suggest that crystal fractionation and accumulation processes can account for much of the diversity observed in the major-element compositions of all lavas.We conclude that the parental basaltic magmas for volcanism in the TVZ and KAHT segments are similar thereby implying grossly similar source mineralogy. We attribute the diversity to secondary processes influencing liquids as they ascended through complex plumbing systems in the sub arc mantle and cross.     

New constraints on the HIMU mantle from neon and helium isotopic compositions of basalts from the Cook–Austral Islands

High ⁴He/³He ratios of 100 000 to 160 000 found at HIMU ocean islands (“high μ,” where μ is the U/Pb ratio) are usually attributed to the presence of recycled oceanic crust in the HIMU mantle source. However, significantly higher ⁴He/³He ratios are expected in recycled crust after residence in the mantle for periods greater than 1 Ga. In order to better understand the helium isotopic signatures in HIMU basalts, we have measured helium and neon isotopic compositions in a suite of geochemically well-characterized basalts from the Cook–Austral Islands. We observe ⁴He/³He ratios ranging from 56 000 to 141 000, suggesting the involvement of mantle reservoirs both more and less radiogenic than the mantle source for mid-ocean ridge basalts (MORBs). In addition, we find that the neon isotopic compositions of HIMU lavas extend from the MORB range to compositions less nucleogenic than MORBs. The Cook-Austral HIMU He–Ne isotopic compositions, along with Sr, Nd, Pb, and Os isotopic compositions, indicate that in addition to recycled crust, a relatively undegassed mantle end-member (e.g., FOZO) is involved in the genesis of these basalts. The association of relatively undegassed mantle material with recycled crust provides an explanation for the close geographical association between HIMU lavas and EM (enriched mantle)-type lavas from this island chain: EM-type signatures represent a higher mixing proportion of relatively undegassed mantle material. Mixing between recycled material and relatively undegassed mantle material may be a natural result of entrainment processes and convective stirring in deep mantle.     

Nitrogen isotope geochemistry of basaltic glasses: implications for mantle degassing and structure?

The nitrogen isotope geochemistry of 15 basaltic glasses has been investigated using stepped heating and high sensitivity static vacuum mass spectrometry. At low temperature (< 600°C) the glasses release small amounts of nitrogen with δ¹⁵N_AIR, averaging −0.3‰, suggesting surficial adsorption of atmospheric nitrogen. At high temperature, usually with a maximum at 1000°C, indigenous nitrogen with a concentration ranging from 0.2 to 2.1 ppm is released. The δ¹⁵N values of this high temperature release show a wide range from −4.5‰ to +15.5‰. There is no correlation between N ppm and δ¹⁵N, and the samples apparently form 3 groups with distinctive δ¹⁵N. Six MORB glasses from the Mid-Atlantic Ridge, East Pacific Rise and Juan de Fuca Ridge define a group with δ¹⁵N = +7.5 ± 1.3‰. In contrast two Indian Ocean MORB glasses (Carlsberg Ridge and Gulf of Aden) gave negative δ¹⁵N averaging −3.2‰. Glasses from Loihi Seamount have high δ¹⁵N averaging +14.0 ± 1.0‰. Comparison of the δ¹⁵N data with the mantle models derived from helium and argon isotope studies suggests that the wide range in δ¹⁵N may reflect in part heterogeneities in the mantle related to its degassing history. It is possible, however, that magmatic degassing processes have also affected nitrogen isotopic compositions, and the data cannot yet be unambiguously interpreted in terms of source variations.     

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)     

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.     

Petrogenesis of anhydrous clinopyroxenite xenoliths and clinopyroxene megacrysts in alkali basalts from the Ganseong area of South Korea

Late Cenozoic alkali basalts in the Ganseong area of South Korea contain abundant ultramafic xenoliths and clinopyroxene megacrysts. Anhydrous clinopyroxene‐rich wehrlite–clinopyroxenites make up the majority of the xenolith population and range from wehrlite through olivine clinopyroxenite to clinopyroxenite. This study investigates the petrogenesis of wehrlite–clinopyroxenite xenoliths and clinopyroxene megacrysts on the basis of petrography and mineral and whole‐rock chemistry. Observations such as an absence of carbonate or apatite, high Ti/Eu ratio, and clinopyroxene‐dominated mineralogy lead us to rule out peridotite–melt reactions as the origin of the Ganseong wehrlites– olivine clinopyroxenites. The whole‐rock compositions (e.g. high abundance of CaO at a given MgO content and low abundance of incompatible elements, such as U, K, P, and Ti compared with mafic melts) indicate that the pyroxenites do not represent crystallized magma itself, but are rather cumulates with a small amount of residual liquid. Anhydrous and orthopyroxene‐free mineral assemblages, crystallization sequence of olivine→clinopyroxene→plagioclase, and mineral chemistries (e.g. low Cr# and high TiO₂ abundances in spinels and high TiO₂ and Na₂O abundances in clinopyroxenes at a given Mg#) suggest that relatively anhydrous intraplate alkaline basalt is the most likely candidate for the parent magma. Texture and compositions of the clinopyroxene megacrysts preclude a cognate origin via high‐pressure crystallization of the host magma. The clinopyroxene megacrysts occupy the Fe‐rich end of the compositional trends defined by wehrlite–pyroxenite clinopyroxenes. Progressive decreases in Mg# and an absence of significant compositional gaps between pyroxenite xenoliths and clinopyroxene megacrysts indicate fractionation and differentiation of a similar parental magma. We suggest that the clinopyroxene megacrysts represent fragments of pegmatitic clinopyroxenites crystallized from more advanced fractionation stages of the evolution of a series of magmatic liquids formed Ganseong wehrlite–clinopyroxenites.