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.     

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.     

Trace elements in ocean ridge basalts

A correlary of sea floor spreading is that the production rate of ocean ridge basalts exceeds that of all other volcanic rocks on the earth combined. Basalts of the ocean ridges bring with them a continuous record in space and time of the chemical characteristics of the underlying mantle. The chemical record is once removed, due to chemical fractionation during partial melting. Chemical fractionations can be evaluated by assuming that peridotite melting has proceeded to an olivine-orthopyroxene stage, in which case the ratios of a number of magmaphile elements in the extracted melt closely match the ratios in the mantle. Comparison of ocean ridge basalts and chondritic meteorites reveals systematic patterns of element fractionation, and what is probably a double depletion in some elements. The first depletion is in volatile elements and is due to high accretion temperatures of a large percentage of the earth from the solar nebula. The second depletion is in the largest, most highly charged lithophile elements (“incompatible elements”), probably because the mantle source of the basalts was melted previously, and the melt, enriched in these elements, was removed. Migration of melt relative to solid under ocean ridges and oceanic plates, element fractionation at subduction zones, and fractional melting of amphibolite in the Precambrian are possible mechanisms for depleting the mantle in incompatible elements. Ratios of transition metals in the mantle source of ocean ridge basalts are close to chondritic, and contrast to the extreme depletion of refractory siderophile elements, the reason for which remains uncertain. Variation of ocean ridge basalt chemistry along the length of the ridge has been correlated with ridge elevation. Thus chemically anomalous ridge segments up to 1000 km long appear to broadly coincide with regions of high magma production (plumes, hot spots). Basalt heterogeneity at a single location indicates mantle heterogeneity on a smaller scale. Variation of ocean ridge basalt chemistry with time has not been established, in fact, criteria for recognizing old oceanic crust in ophiolite terrains are currently under debate. The similarity of rare earth element patterns in basalt from ocean ridges, back-arc basins, some young island arcs, and some continental flood basalts illustrates the dangers of tectonic labeling by rare earth element pattern.     

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.     

Asthenospheric percolation of alkaline melts beneath the St. Paul region (Central Atlantic Ocean)

Two peridotite suites collected by submersible in the equatorial Atlantic Ocean (Hekinian et al., 2000) were studied for textures, modes, and in situ major and trace element compositions in pyroxenes. Dive SP12 runs along the immersed flank of the St. Peter and Paul Rocks islets where amphibole-bearing, ultramafic mylonites enriched in alkalies and incompatible elements are exposed (Roden et al., 1984), whereas dive SP03 sampled a small intra-transform spreading centre situated about 370 km east of the St. Peter and Paul Rocks. Both suites are characterized by undeformed, coarse-grained granular textures typical of abyssal peridotites, derived from residual mantle after ～ 15% melting of a DMM source, starting in the garnet stability field. Trace element modelling, textures and lack of mineral zoning indicate that the residual peridotites were percolated, reacted and refertilized by ～ 2.6% partially aggregated melts in the uppermost level of the melting region. This relatively large amount of refertilization is in agreement with the cold and thick lithosphere inferred by previous studies. Freezing of trapped melts occurred as the peridotite entered the conductive layer, resulting in late-stage crystallization of olivine, clinopyroxene, spinel, ± plagioclase. Chondrite-normalized REE patterns in clinopyroxenes from SP03 indicate that they last equilibrated with (ultra-) depleted partial melts. In contrast, REE concentrations in clinopyroxenes from SP12 display U and S shaped LREE-enriched patterns and the calculated compositions of the impregnating melts span the compositional range of the regional basalts, which vary from normal MORB to alkali basalt sometimes modified by chromatographic fractionation with no, or very limited, mineral reaction. Thus the mylonitic band forming the St. Peter and St. Paul Rocks ridge is not a fragment of subcontinental lithospheric mantle left behind during the opening of the Central Atlantic, nor the source of the alkaline basalts as previously suggested. Rather, dive SP12 sampled residual peridotites of normal MORB mantle that were located close to channels transporting alkali basalts. Reacted melts escaping from these channels, infiltrated, and locally equilibrated with, the peridotite matrix by ion exchange reactions. Relicts of the source of the alkaline basalts were not sampled but our study suggests that it was a component of the MORB mantle underlying the St. Paul region.     

Deep melting and sodic metasomatism underneath the highly oblique-spreading Lena Trough (Arctic Ocean)

Abyssal peridotites collected along the highly oblique-spreading Lena Trough north of Greenland and Spitsbergen have mineral compositions that are similar to residual abyssal peridotites, except for high sodium concentrations in clinopyroxene (cpx). Most samples are lherzolites with light rare earth element (REE)-depleted cpx trace element patterns, but significantly fractionated middle to heavy REE ratios at relatively high heavy REE concentrations. Such characteristics can only be explained by initial melting of a garnet peridotite followed by low degrees of melting in the stability field of spinel peridotite. The residual garnet signature requires either a high potential temperature of the upwelling mantle, or elevated solidus-lowering water contents. The limited spinel field melting suggests a deep cessation of melt extraction, possibly because of the presence of a thick lithospheric cap. This is consistent with the extremely low effective spreading rate and the vicinity to a passive continental margin, which allow conductive cooling to reach deeper levels than commonly estimated for faster mid-ocean ridges. High sodium concentrations in cpx are neither explainable by melt refertilization, nor by a simple diffusion mechanism. The efficient fractionation of sodium from the light REE requires post-melting metasomatism, which is typically restricted to the subcontinental lithosphere. This might imply that the Lena Trough peridotites represent unroofed subcontinental mantle, from which no melt was extracted during the opening of the Lena Trough. It is more likely that sodic metasomatism occurred after partial melting underneath the Lena Trough, and that such an enrichment process is responsible for elevated sodium concentrations in abyssal peridotites elsewhere. Sodium in cpx of residual peridotites can therefore not serve as an indicator of partial melting or melt refertilization.     

Complete mantle section of a slow-spreading ridge-derived ophiolite: An example from the Isabela ophiolite in the Philippines

Abstract   The Isabela ophiolite shows a complete ophiolite sequence exposed along the eastern coast of northern Luzon, the Philippines. It forms the Cretaceous basement complex for the northeastern Luzon block. This ophiolite is located at the northern end of a trail of ophiolites and ophiolitic bodies along the eastern margin of the Philippine Mobile Belt. This paper presents new findings regarding the nature and characteristics of the Isabela ophiolite. Peridotites from the Isabela ophiolite are relatively fresh and are composed of spinel lherzolites, clinopyroxene-rich harzburgites, depleted harzburgites and dunites. The modal composition, especially the pyroxene content, defines a northward depletion trend from fertile lherzolite to clinopyroxene-rich harzburgites and more refractory harzburgites. Variation in modal composition is accompanied by petrographic textural variations. The chromium number of spinel, an indicator of the degree of partial melting, concurs with petrographic observations. Furthermore, the Isabela ophiolite peridotites are similar in spinel and olivine major-element geochemistry and clinopyroxene rare earth-element composition to abyssal peridotites from modern mid-oceanic ridges. Petrological and mineral compositions suggest that the Isabela ophiolite is a transitional ophiolite subtype, with the fertile lherzolites representing lower sections of the mantle column that are usually absent in most ophiolitic massifs. The occurrence of the fertile peridotite presents a rare opportunity to document the lower sections of the ophiolitic mantle. The variability in composition of the peridotites in one continuous mantle section may also represent a good analogy of the melting column in the present-day mid-oceanic ridges.     

Diapirism of depleted peridotite — a model for the origin of hot spots

A model is proposed for the origin of hot spots that depends on the existence of major-element heterogeneities in the mantle. Generation of basaltic crust at spreading centers produces a layer of residual peridotite ～20–25 km thick directly beneath the crust which is depleted in Fe/Mg, TiO₂, CaO, Al₂O₃, Na₂O and K₂O, and which has a slightly lower density than undepleted peridotite beneath it. Upon recycling of this depleted peridotite back into the deep mantle at subduction zones, it becomes gravitationally unstable, and tends to rise as diapirs through undepleted peridotite. For a density contrast of 0.05 g cm^?3, a diapir 60 km in diameter would rise at roughly 8 cm y^?1, and could transport enough heat to the base of the lithosphere to cause melting and volcanism at the surface. Hot spots are thus viewed as a passive consequence of mantle convection and fractionation at spreading centers rather than a plate-driving force.It is suggested that depleted diapirs exist with varying amounts of depletion, diameters, upward velocities and source volumes. Such variations could explain the occurrence of hot spots with widely varying lifetimes and rates of lava production. For highly depleted diapirs with very low Fe/Mg, the diapir would act as a heat source and the asthenosphere and lower lithosphere drifting across the diapir would serve as the source region of magmas erupted at the surface. For mildly depleted diapirs with Fe/Mg only slightly less than in normal undepleted mantle, the diapir could provide not only the source of heat but also most or all of the source material for the erupted magmas. The model is consistent with isotopic data that require two separate and ancient source regions for mid-ocean ridge and oceanic island basalts. The source for mid-ocean ridge basalts is considered to be material upwelling at spreading centers from the deep mantle. This material forms the oceanic lithosphere. Oceanic island basalts are considered to be derived from varying mixtures of sublithospheric and lower lithospheric material and the rising diapir itself.     

Nd-isotope systematics of ∼2.7 Ga adakites, magnesian andesites, and arc basalts, Superior Province: evidence for shallow crustal recycling at Archean subduction zones

An association of adakite, magnesian andesite (MA), and Nb-enriched basalt (NEB) volcanic flows, which erupted within ‘normal’ intra-oceanic arc tholeiitic to calc-alkaline basalts, has recently been documented in ∼2.7 Ga Wawa greenstone belts. Large, positive initial ?_Nd values (+1.95 to +2.45) of the adakites signify that their basaltic precursors, with a short crustal residence, were derived from a long-term depleted mantle source. It is likely that the adakites represent the melts of subducted late Archean oceanic crust. Initial ?_Nd values in the MA (+0.14 to +1.68), Nb-enriched basalts and andesites (NEBA) (+1.11 to +2.05), and ‘normal’ intra-oceanic arc tholeiitic to calc-alkaline basalts and andesites (+1.44 to +2.44) overlap with, but extend to lower values than, the adakites. Large, tightly clustered ?_Nd values of the adakites, together with Th/Ce and Ce/Yb systematics of the arc basalts that rule out sediment melting, place the enriched source in the sub-arc mantle. Accordingly, isotopic data for the MA, NEBA, and ‘normal’ arc basalts can be explained by melting of an isotopically heterogeneous sub-arc mantle that had been variably enriched by recycling of continental material into the shallow mantle in late Archean subduction zones up to 200 Ma prior to the 2.7 Ga arc. If the late Archean Wawa adakites, MA, and basalts were generated by similar geodynamic processes as their counterparts in Cenozoic arcs, involving subduction of young and/or hot ocean lithosphere, then it is likely that late Archean oceanic crust, and arc crust, were also created and destroyed by modern plate tectonic-like geodynamic processes. This study suggests that crustal recycling through subduction zone processes played an important role for the generation of heterogeneity in the Archean upper mantle. In addition, the results of this study indicate that the Nd-isotope compositions of Archean arc- and plume-derived volcanic rocks are not very distinct, whereas Phanerozoic plumes and intra-oceanic arcs tend to have different Nd-isotopic compositions.     

Petrography and geochemistry of basaltic rocks from the Conrad fracture zone on the America-Antarctica Ridge

Intrusive and extrusive basaltic rocks have been dredged from the Conrad fracture zone (transecting the slow-spreading America-Antarctica Ridge). The majority of rocks recovered are holocrystalline with the dominant mineral assemblage being plagioclase plus clinopyroxene with or without minor Fe-Ti oxides (olivine occurs in only three samples) and many of the samples show evidence of extensive alteration. Secondary minerals include chlorite, actinolite, K- and Na-feldspar, analcite and epidote. In terms of bulk chemistry the rocks are characterized by their generally evolved and highly variable compositions (e.g.Mg^*=0.65?0.35;TiO₂=0.7?3.6%;Zr=31?374ppm;Nb=<3?21ppm;Y=17?96ppm;Ni=100?9ppm), but with respect to the immobile incompatible element ratios (e.g. Zr/Nb, Y/Nb, La/Sm) are similar to “normal” or depleted mid-oceanic ridge basalts.Quantitative major and trace element modelling indicate that most of the variation observed can be attributed to low-pressure fractional crystallization of plagioclase plus clinopyroxene in approximately equal proportions with or without minor Fe-Ti oxides. The range in composition can be accounted for by up to 76% fractional crystallization. Although ferrobasalts have not frequently been associated with slow spreading ridges, the extreme differentiation observed in the Conrad fracture zone basalts implies some additional constraint other than spreading rate on the formation of ferrobasalt and reaffirms the importance of extensive crustal differentiation during the production of this basalt type.     

Volcanic Markers of the Post-Subduction Evolution of Baja California and Sonora, Mexico: Slab Tearing Versus Lithospheric Rupture of the Gulf of California

The study of the geochemical compositions and K-Ar or Ar-Ar ages of ca. 350 Neogene and Quaternary lavas from Baja California, the Gulf of California and Sonora allows us to discuss the nature of their mantle or crustal sources, the conditions of their melting and the tectonic regime prevailing during their genesis and emplacement. Nine petrographic/geochemical groups are distinguished: ??regular?? calc-alkaline lavas; adakites; magnesian andesites and related basalts and basaltic andesites; niobium-enriched basalts; alkali basalts and trachybasalts; oceanic (MORB-type) basalts; tholeiitic/transitional basalts and basaltic andesites; peralkaline rhyolites (comendites); and icelandites. We show that the spatial and temporal distribution of these lava types provides constraints on their sources and the geodynamic setting controlling their partial melting. Three successive stages are distinguished. Between 23 and 13 Ma, calc-alkaline lavas linked to the subduction of the Pacific-Farallon plate formed the Comondú and central coast of the Sonora volcanic arc. In the extensional domain of western Sonora, lithospheric mantle-derived tholeiitic to transitional basalts and basaltic andesites were emplaced within the southern extension of the Basin and Range province. The end of the Farallon subduction was marked by the emplacement of much more complex Middle to Late Miocene volcanic associations, between 13 and 7 Ma. Calc-alkaline activity became sporadic and was replaced by unusual post-subduction magma types including adakites, niobium-enriched basalts, magnesian andesites, comendites and icelandites. The spatial and temporal distribution of these lavas is consistent with the development of a slab tear, evolving into a 200-km-wide slab window sub-parallel to the trench, and extending from the Pacific coast of Baja California to coastal Sonora. Tholeiitic, transitional and alkali basalts of subslab origin ascended through this window, and adakites derived from the partial melting of its upper lip, relatively close to the trench. Calc-alkaline lavas, magnesian andesites and niobium-enriched basalts formed from hydrous melting of the supraslab mantle triggered by the uprise of hot Pacific asthenosphere through the window. During the Plio-Quaternary, the ??no-slab?? regime following the sinking of the old part of the Farallon plate within the deep mantle allowed the emplacement of alkali and tholeiitic/transitional basalts of deep asthenospheric origin in Baja California and Sonora. The lithospheric rupture connected with the opening of the Gulf of California generated a high thermal regime associated to asthenospheric uprise and emplaced Quaternary depleted MORB-type tholeiites. This thermal regime also induced partial melting of the thinned lithospheric mantle of the Gulf area, generating calc-alkaline lavas as well as adakites derived from slivers of oceanic crust incorporated within this mantle.     

Partial melting controls on the northwest Kyushu basalts from Saga-Futagoyama

Abstract   The major element and compatible trace element compositions of the northwest Kyushu basalts (NWKBs) collected from Saga-Futagoyama were analyzed to examine the petrogenesis of these basalts. Although nepheline-normative alkaline basalts are not found in the basalts from Saga-Futagoyama, the Saga-Futagoyama basalts almost cover the major element variations of NWKBs. The basalts can be chemically divided into two groups: an Fe-poor group (IPG) and an Fe-rich group (IRG). The compositional variation of IPG basalts is essentially controlled by the partial melting of the source as suggested by the following: (i) bulk rock MgO, FeO and NiO compositions indicate that some IPG samples were equilibrated with mantle olivine; and (ii) correlations between Al₂O₃, CaO and MgO are consistent with those of experimental partial melts of peridotites. The inconsistent behaviors of the elements compatible with clinopyroxene (Cpx), such as V (Sc and Cu), preclude the significant role of the fractional crystallization of Cpx and spinel in IPG variation. IPG basalts have low Al and high Fe concentrations compared to the products of melting experiments involving peridotites and pyroxenites, suggesting that the IPG source would have a lithology and bulk rock composition different from those of typical peridotites and pyroxenites. IRG basalts have negative correlations between Fe₂O₃* and MgO, and between V and Fe₂O₃*/MgO, indicating that IRG basalts would have fractionated Cpx. However, the anomalously Fe-rich feature of IRG basalts compared with NWKBs collected from other areas suggests that the role of Cpx fractionation in NWKBs is minor. Relatively low melting temperatures would have principally caused the large chemical variation of NWKBs.     

Petrogenetic relationships of acid and basic rocks in iceland: Sr-isotopes and rare-earth elements in late and postglacial volcanics

Strontium isotope ratios and rare-earth element abundances have been measured in acid, intermediate and basic rocks from three late to postglacial volcanic complexes, and several other postglacial basalts in Iceland. Late and postglacial basalts in Iceland have been generated from a source region which is essentially homogeneous with respect to⁸⁷Sr/⁸⁶Sr. The mean⁸⁷Sr/⁸⁶Sr ratio for the basalts analysed is 0.70328 and the range is from 0.70317 ± 6to0.70334 ± 5 (2σ).Acid rocks from the Kerlinganfjöll and Namafjall volcanic complexes have⁸⁷Sr/⁸⁶Sr ratios which are indistinguishable from analysed basalts from the same complexes. However, intermediate and acid rocks from the Torfajökull complex have significantly higher⁸⁷Sr/⁸⁶Sr ratios and could not have been derived by fractional crystallization from basaltic magmas similar to those found in the same complex. These latter rocks have most probably been produced by remelting of Tertiary gabbroic rocks in Layer 3. Most of the basalts analysed have higher total rare-earth element abundances than typical dredged ocean-ridge tholeiites, and show less light rare-earth depletion. Intermediate and acid compositions show overall higher abundances and light rare-earth enrichments. The measured rare-earth abundances are compared with abundances generated by differential partial melting of various model source regions.It is shown that both the tholeiitic and alkali basalt compositions could be generated from the same source material by different degrees of partial melting. Variable partial melting of gabbroic material may account for the rare-earth element abundances of both the rhyolitic rocks (small degrees of melting) and the intermediate rocks (more extensive melting).     

The water content and hydrogen isotope composition of continental lithospheric mantle and mantle-derived mafic igneous rocks in eastern China

The water contents of minerals and whole-rock in mantle-derived xenoliths from eastern China exhibit large variations and are generally lower than those from other on- and off-craton lithotectonic units. Nevertheless, the water contents of mineral and whole-rock in Junan peridotite xenoliths, which sourced from the juvenile lithospheric mantle, are generally higher than those elsewhere in eastern China. This suggests that the initial water content of juvenile lithospheric mantle is not low. There is no obvious correlation between the water contents and Mg^# values of minerals in the mantle xenoliths and no occurrence of diffusion profile in pyroxene, suggesting no relationship between the low water content of mantle xenolith and the diffusion loss of water during xenolith ascent with host basaltic magmas. If the subcontinental lithospheric mantle (SCLM) base is heated by the asthenospheric mantle, the diffusion loss of water is expected to occur. On the other hand, extraction of basaltic melts from the SCLM is a more efficient mechanism to reduce the water content of xenoliths. The primary melts of Mesozoic and Cenozoic basalts in eastern China have water contents, as calculated from the water contents of phenocrysts, higher than those of normal mid-ocean ridge basalts (MORB). The Mesozoic basalts exhibit similar water contents to those of island arc basalts, whereas the Cenozoic basalts exhibit comparable water contents to oceanic island basalts and backarc basin basalts with some of them resembling island arc basalts. These observations suggest the water enrichment in the mantle source of continental basalts due to metasomatism by aqueous fluids and hydrous melts derived from dehydration and melting of deeply subducted crust. Mantle-derived megacrysts, minerals in xenoliths and phenocrysts in basalts from eastern China also exhibit largely variable hydrogen isotope compositions, indicating a large isotopic heterogeneity for the Cenozoic SCLM in eastern China. The water content that is higher than that of depleted MORB mantle and the hydrogen isotope composition that is deviated from that of depleted MORB mantle suggest that the Cenozoic continental lithospheric mantle suffered the metasomatism by hydrous melts derived from partial melting of the subducted Pacific slab below eastern China continent. The metasomatism would lead to the increase of water content in the SCLM base and then to the decrease of its viscosity. As a consequence, the SCLM base would be weakened and thus susceptible to tectonic erosion and delamination. As such, the crust-mantle interaction in oceanic subduction channel is the major cause for thinning of the craton lithosphere in North China.     

Geochemistry of peridotite xenoliths in alkali basalts from Jeju Island, Korea

Abstract   Ultramafic xenoliths in alkali basalts from Jeju Island, Korea, are mostly spinel lherzolites with subordinate amounts of spinel harzburgites and pyroxenites. The compositions of major oxides and compatible to moderately incompatible elements of the Jeju peridotite xenoliths suggest that they are residues after various extents of melting. The estimated degrees of partial melting from compositionally homogeneous and unfractionated mantle to form the residual xenoliths reach 30%. However, their complex patterns of chondrite-normalized rare earth element, from light rare earth element (LREE)-depleted through spoon-shaped to LREE-enriched, reflect an additional process. Metasomatism by a small amount of melt/fluid enriched in LREE followed the former melt removal, which resulted in the enrichment of the incompatible trace elements. Sr and Nd isotopic ratios of the Jeju xenoliths display a wide scatter from depleted mid-oceanic ridge basalt (MORB)-like to near bulk-earth estimates along the MORB–oceanic island basalt (OIB) mantle array. The varieties in modal proportions of minerals, (La/Yb)_N ratio and Sr-Nd isotopes for the xenoliths demonstrate that the lithospheric mantle beneath Jeju Island is heterogeneous. The heterogeneity is a probable result of its long-term growth and enrichment history.     

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.     

Lead isotope study of orogenic lherzolite massifs

Orogenic lherzolites allow for almost “in-situ” observation of mantle isotopic heterogeneities on a restricted geographical scale, in contrast to basalts for which melting processes have averaged original mantle compositions over uncertain scales. Pb isotopes from whole rocks and clinopyroxenes from the massifs of Lherz (Pyrenees), Lanzo (Alps), Beni Bousera (Morocco) and Zabargad (Red Sea) show internal heterogeneities that encompass the entire range of variation observed in oceanic basalts. Some depleted lherzolites have a very unradiogenic composition similar to that of the most depleted ridge tholeiites. Pyroxenites from mafic layers generally have more radiogenic compositions, some of them comparable to the most radiogenic oceanic island results. The isotopic differences between lherzolites and pyroxenites vanish where layers are very closely spaced ( < 2 cm). In this case, the lherzolites may have equilibrated with the more Pb-rich pyroxenites through solid-state diffusion under mantle conditions. These results directly illustrate the smallest scales at which Pb isotopic heterogeneity may survive within the mantle.The genesis of these heterogeneities are discussed within the framework of the “marble cake” mantle model [1], where lherzolites are residues left over after oceanic crust extraction, whereas pyroxenites represent either basaltic or cumulate portions of the oceanic crust, reinjected by subduction and stretched by solid-state mixing during mantle convection. The Pb isotope data suggest that each massif was involved in several cycles of convective overturn, segregation and reinjection of the oceanic crust, during periods well over 1 Ga.If the upper mantle is made of interlayered radiogenic and unradiogenic layers, basalt heterogeneities may result from preferential melt-extraction from different layers depending on the degree of melting, as well as from large-scale, plume-related mantle heterogeneities. Orogenic lherzolites therefore allow direct observation of disseminated small-scale heterogeneities previously inferred from observations of oceanic basalts from seamounts and ridges.     

Paleozoic basaltic komatiite and ocean-floor type basalts from northeastern Newfoundland

Basic pillow lavas from northeastern Newfoundland are shown to be chemically similar to basaltic komatiites and ocean-floor basalts. New trace element data presented for basaltic komatiites indicate that they were derived from a magma more primitive than that producing ocean-floor basalts. A model for the derivation of basaltic komatiite by extensive partial melting of pyrolitic upper mantle at sites of plate separation is proposed.     

Peridotites from the southern Mariana forearc: Heterogeneous fluid supply in mantle wedge

Detailed petrological work was carried out on serpentinized peridotite dredged and sampled by submersible from the southern part of the Mariana Trench to reveal the nature of the mantle wedge in the southern Mariana forearc. The southern part of the Mariana Trench is important in that we should expect to find a transect of a typical island arc structure; that is, from east to west, the Mariana forearc, the Mariana arc proper, the Mariana Trough (active back-arc spreading center), and the West Mariana Ridge (remnant arc). The most striking feature of peridotites from the southern part of the trench is that primary hornblende is a major constituent mineral in many specimens. Thus, the peridotite samples are divided into anhydrous (A-type), hydrous (H-type) and intermediate (I-type) groups. Petrological data suggest that each type of peridotite is a residue of extensive partial melting in the upper mantle. It is argued here that the I- and H-type peridotites were modified from `proto-A-type peridotite' by fluid infiltration. The fluid was enriched in Al, Ti, Fe, and alkalis, and may have caused changes in mineral and bulk chemical compositions of the peridotites. A-type peridotite derives from the `proto-A-type peridotite' directly, without any fluid contamination. After the formation of the `proto-A-, I-, and H-type peridotites', lower-temperature fluids, probably of seawater origin, produced retrograde metamorphism and alteration including serpentinization. The mantle wedge in the southern Mariana forearc was heterogeneous in fluid supply.     

Amphibole-bearing basalts from the submarine volcano Kick’em-Jenny in the lesser antilles Island arc

An oceanographic survey by H.M.S. Hecla of the 1974 active submarine volcano (12°18′N and 61°38′W) revealed a crater at 190 m below sea level and bottom-sampling yielded fresh olivine basalt pyroclastics with phenocrysts of olivine, plagioclase and clinopyroxene. Megacrysts of amphilbole, up to 16 modal percent, are subsilicic and nepheline-normative ferroan pargasites. The mineral assemblage Ol+Cpx+Pl+Amph appears to have been in equilibrium in the Kick’em-Jenny melt prior to eruption, although published experimental studies on hydrous (H₂O-saturated) or anhydrous alkali basaltic compositions have not yielded this mineral assemblage at any pressure. Interpolation between the experimentally determined phase relationships for dry and water-saturated alkali basaltic liquids indicates, however, that in an isobaric section at 5 kb the observed assemblage can exist in the water-undersaturated region. The Kick’em-Jenny olivine basalts belong to a suite of variably undersaturated basaltic rocks including alkali picrites and basanites, common in Grenada and the southern Grenadines, but although the available evidence indicates the importance of the presence of water in the genesis of these melts, their origin seems most likely to be associated with partial melting of upper mantle material rather than melting of amphibolite in an underthrust lithospheric slab.