The basaltic to trachydacitic upper Diliman Tuff in Manila: Petrogenesis and comparison with deposits from Taal and Laguna Calderas

The basaltic to trachydacitic (50–65 wt.% SiO₂) upper Diliman Tuff is the youngest deposit of a sequence of tuffaceous deposits in Metro Manila. The deposit is located north of Taal Caldera and northwest of Laguna Caldera, which are both within the Southwest Luzon Volcanic Field. Chemical variations in the pumice fragments within the upper Diliman Tuff include medium-K basalt to basaltic andesite, high-K basaltic andesite to andesite and trachyandesite to trachydacite. Magma mixing/mingling is ubiquitous and is shown by banding textures in some pumice fragments, considerable range in groundmass glass composition (54 to 65 wt.% SiO₂) in a single pumice fragment, and zoning in plagioclase phenocrysts. Simple binary mixing modeling and polytopic vector analysis were used to further evaluate magma mixing. Trace-element variations are inconsistent with the medium-K and high-K magmas being related by crystal fractionation. The medium-K basalts represent hotter intrusions, which induced small degrees of partial melting in older crystallized medium-K basaltic material within the crust to produce the high-K magmas. All melts likely differentiated in the crust but the emplaced and new basaltic intrusions originated from the mantle wedge and were generated by subduction zone processes. The volcanic source vent for the upper Diliman Tuff has not been identified. In comparisons with the deposits from adjacent Taal and Laguna Calderas it is chemically distinct with respect to both major- and trace-element concentrations.     

Origin and ascent history of unusually crystal-rich alkaline basaltic magmas from the western Pannonian Basin

The last eruptions of the monogenetic Bakony-Balaton Highland Volcanic Field (western Pannonian Basin, Hungary) produced unusually crystal- and xenolith-rich alkaline basalts which are unique among the alkaline basalts of the Carpathian–Pannonian Region. Similar alkaline basalts are only rarely known in other volcanic fields of the world. These special basaltic magmas fed the eruptions of two closely located volcanic centres: the Bondoró-hegy and the Füzes-tó scoria cone. Their uncommon enrichment in diverse crystals produced unique rock textures and modified original magma compositions (13.1–14.2 wt.% MgO, 459–657 ppm Cr, and 455–564 ppm Ni contents). Detailed mineral-scale textural and chemical analyses revealed that the Bondoró-hegy and Füzes-tó alkaline basaltic magmas have a complex ascent history, and that most of their minerals (～30 vol.% of the rocks) represent foreign crystals derived from different levels of the underlying lithosphere. The most abundant xenocrysts, olivine, orthopyroxene, clinopyroxene, and spinel, were incorporated from different regions and rock types of the subcontinental lithospheric mantle. Megacrysts of clinopyroxene and spinel could have originated from pegmatitic veins/sills which probably represent magmas crystallized near the crust–mantle boundary. Green clinopyroxene xenocrysts could have been derived from lower crustal mafic granulites. Minerals that crystallized in situ from the alkaline basaltic melts (olivine with Cr-spinel inclusions, clinopyroxene, plagioclase, and Fe–Ti oxides) are only represented by microphenocrysts and overgrowths on the foreign crystals. The vast amount of peridotitic (most common) and mafic granulitic materials indicates a highly effective interaction between the ascending magmas and wall rocks at lithospheric mantle and lower crustal levels. However, fragments from the middle and upper crust are absent from the studied basalts, suggesting a change in the style (and possibly rate) of magma ascent in the crust. These xenocryst- and xenolith-rich basalts yield divers tools for estimating magma ascent rate that is important for hazard forecasting in monogenetic volcanic fields. According to the estimated ascent rates, the Bondoró-hegy and Füzes-tó alkaline basaltic magmas could have reached the surface within hours to few days, similarly to the estimates for other eruptive centres in the Pannonian Basin which were fed by “normal” (crystal and xenoliths poor) alkaline basalts.     

Mineralogy and chemistry of modern orogenic lavas — some statistics and implications

Island arc and continental margin (i.e. western Americas) lavas are divided (based on raw data from literature) into basalts (defined by absence of Ca-poor pyroxene, dominated by quartz-normative tholeiites); basaltic andesites and andesites (subdivided on basis of breaks in SiO₂ histogram and taken as <56% and 56–63% SiO₂; Ca-poor pyroxene present; amphibole and biotite absent); and hornblende (±biotite) lavas, which prove to be mainly relatively silicic andesites. Relative proportions of these types are (576 samples): 23% basalts, 29% basaltic andesites; 30% andesites; 18% hornblende andesites. The compilation emphasizes the dominance of calcic plagioclase (labradorite-anorthite) amongst the phenocryst phases. Pyroxenes are largely augite and hypersthene (En_60–75); olivine (Fo_65–85) is common through all compositions. There is an overall close similarity in chemistry and mineralogy between continental margin and island arc lavas, although small consistent differences are apparent (e.g. K₂O, TiO₂, P₂O₅).Modal data indicate that 70% of lavas are phenocryst-rich (20–60 vol.%), and that phenocryst contents show a bimodal distribution. Statistically and petrologically significant correlations are found between mineralogy and rock chemistry, most notably between total rock Al₂O₃ and modal phenocrystic plagioclase (found in all data groups, except hornblende andesites). This, and related data and correlations, indicate that the majority of orogenic magmas are modified by crystal fractionation (including crystal accumulation) processes dominated by plagioclase, and interpreted to occur under relatively low pressures. Dominance of plagioclase suggests phenocryst precipitation occurs typically in water-undersaturated magmas.     

Origin of rhyolite by crustal melting and the nature of parental magmas in the Oligocene Conejos Formation,San Juan Mountains,Colorado, USA

Four closely spaced volcanoes (Summer Coon; Twin Mountains; Del Norte; Carnero Creek) form the east-central cluster of Conejos volcanic centers. These Conejos rocks range from high-K basaltic andesite to rhyolite, with andesite volumetrically the most abundant. Summer Coon and Twin Mountains are composite volcanoes. The Del Norte and Carnero Creek volcanoes are deeply eroded dacite shields. Rhyolite (10% of our Conejos analyses but a much smaller percentage by volume) is only known from Summer Coon and Twin Mountains volcanoes, although high-SiO₂ dacite occurs in the Del Norte volcano. The younger Hinsdale Formation contains a related series ranging from transitional basalt to high-K andesite; we use Hinsdale Formation analyses to represent Conejos parental magmas.Conejos and Hinsdale magmas evolved through AFC processes: Basalt, after interacting with lower crust, assimilated low K/Rb crust, similar in some ways to Taylor and McLennan (Taylor, S.R., and McLennan, S.M., 1985, The continental crust: its composition and evolution. Oxford, Blackwell Scientific.) model upper crust; main series basaltic andesite fractionated to high-K andesite; rhyolite was produced by melting of high K/Ba upper crustal rocks similar to granite gneiss known from inclusions and basement outcrops. Some rhyolite may have been back-mixed into fractionating andesite and dacite. Field evidence for assimilation includes sanidinite-facies, partially melted, gneiss blocks up to 1 m in diameter. Temperature estimates (1100–900 ° C) from two-pyroxene equilibria are consistent with this interpretation, as are the sparsely porphyritic nature of the most-evolved rhyolites and the absence of phenocrystic alkali feldspar.Our study supports the conclusions of previous workers on AFC processes in similar, but generally more mafic, Conejos magmas of the southeastern San Juan Mountains. Our results, however, emphasize the importance of crustal melting in the generation of Conejos rhyolite. We further speculate that Conejos magmatism, and the San Juan Volcanic Field (SJVF) in general, may represent an early phase of Rio Grande rift magmatism, the orogenic geochemical signature of the series having been generated through multi-level and extensive assimilation of varied Precambrian orogenic and anorogenic rocks.     

Nd-Sr systematics of the Setouchi volcanic rocks,southwest Japan: a clue to the origin of orogenic andesite

Twenty-three volcanic rocks from the Setouchi volcanic belt, southwest Japan, were analyzed for Nd and Sr isotopic compositions for the purpose of examining the genetic relationships among the basalt, high-magnesium andesite (HMA) and evolved porphyritic andesite. The andesites have higher⁸⁷Sr/⁸⁶Sr (0.70487–0.70537) and lower¹⁴³Nd/¹⁴⁴Nd (0.512509–0.512731) than the basalts, i.e., 0.70408–0.70468 and 0.512691–0.512830, respectively. This result confirms earlier conclusions obtained from petrologic study that the andesites cannot be fractionation products of basaltic magma but that the andesitic and basaltic magmas were generated independently. On the basis of melting experiments for HMA and basalt, it is inferred that there is an isotopically stratified mantle beneath southwest Japan. Evolved porphyritic andesites have essentially identical Sr and Nd isotopic ratios to HMA and can be derived by fractionation of primary andesitic magma. A model to produce orogenic andesite is proposed on petrologic, experimental and isotopic bases.     

The eruptive history of the Mascota volcanic field,western Mexico: Age and volume constraints on the origin of andesite among a diverse suite of lamprophyric and calc-alkaline lavas

The Mascota volcanic field is located in the Jalisco Block of western Mexico, where the Rivera Plate subducts beneath the North American Plate. It spans an area of ∼ 2000 km² and contains ∼ 87 small cones and lava flows of minette, absarokite, basic hornblende lamprophyre, basaltic andesite, and andesite. There are no contemporary dacite or rhyolite lavas. New ⁴⁰Ar/³⁹Ar ages are presented for 35 samples, which are combined with nine dates from the literature to document the eruptive history of this volcanic field. The oldest lavas (2.4 to 0.5 Ma) are found in the southern part of the field area, whereas the youngest lavas (predominantly < 0.5 Ma) are found in the northern portion. On the basis of these ages, field mapping, and the use of ortho aerial photographs and digital elevation models, it is estimated that a combined volume of 6.8 ± 3.1 km³ erupted in the last 2.4 Myr, which leads to an average eruption rate of ∼ 0.003 km³/kyr, and an average volume per eruptive unit of < 0.1 km³. The dominant lava type is andesite (2.1 ± 0.9 km³), followed by absarokite (1.6 ± 0.8 km³), basaltic andesite (1.2 ± 0.5 km³), basic hornblende lamprophyre (1.0 ± 0.4 km³), and minette (0.9 ± 0.5 km³). Thus, the medium-K andesite and basaltic andesite comprise approximately half (49%) of the erupted magma, with twice as much andesite as basaltic andesite, and they occur in close spatial and temporal association with the highly potassic, lamprophyric lavas. There is no time progression to the type of magma erupted. A wide variety of evidence indicate that the high-MgO (8–9 wt.% ) basaltic andesites (52–53% wt.% SiO₂) were formed by H₂O flux melting of the asthenopheric arc mantle wedge, whereas the mafic minettes and absarokites were formed by partial melting (induced by thermal erosion) of depleted lithospheric mantle containing phlogopite-bearing veins. There is only limited differentiation of the potassic magmas, with none more evolved than 55.4 wt.% SiO₂ and 4.4 wt.% MgO. This may be attributable to rapid crystallization of the mantle-derived melts in the deep crust, owing to their low volumes. Thus, the andesites (58–63 wt.% SiO₂) are notable for being both the most voluminous and the most evolved of all lava types in the Mascota volcanic field, which is not consistent with their extraction from extensively crystallized (60–70%), low-volume intrusions. Instead, the evidence supports the origin of the andesites by partial melting of amphibolitized, mafic lower crust, driven by the emplacement of the minettes, absarokites, and the high-Mg basaltic andesites.     

Middle Miocene to Quaternary primary basalt and high magnesian andesite magmas of North Hokkaido, Japan: Source mantle characteristics and degrees of partial melting

Abstract   Middle Miocene to Quaternary primitive basalts and high magnesian andesite (HMA) in North Hokkaido resulted from three periods of intense volcanism; early-stage (12–10 Ma), middle-stage (9–7 Ma) and late-stage (3–0 Ma). Based on the chemical compositions of olivines and chromian spinels and bulk chemistry of the primitive rocks, we examined depths of segregation of the calculated primary magmas and the degrees of partial melting of the source mantle. In the context of asthenospheric mantle upwelling, petrological data from the present study can be accounted for by the secular change in the depth of magma segregation from the upwelled asthenospheric mantle, which is composed of fertile peridotite. Thus, the early-stage primary magmas were generated by higher degrees of partial melting of the shallower part of hot asthenospheric mantle, whereas the middle- and late-stage primary magmas resulted from lower degrees of partial melting of a deeper part of the asthenospheric mantle. The early-stage HMA magma was generated by partial melting of the remnant subcontinental lithospheric mantle composed of refractory peridotite. This melting might have resulted from an increased geothermal gradient caused by upwelling of hot asthenosphere.     

Origin of some calc-alkalic andesites in the Japanese Islands

Origin of calc-alkalic andesite in the Japanese Islands is reviewed on the basis of the recent trace element data and new experimental results. It is suggested that calc-alkalic andesites in the Japanese Islands have at least four different origins; (1) fractional crystallization with separation of magnetite of high-alumina basalt magma, (2) partial melting of hydrous upper mantle peridotite (for magnesian andesite), (3) fractional crystallization with separation of olivine and/or orthopyroxene of magnesian andesite magma and (4) mixing of dacitic and basaltic magmas. Emphasis is placed on the possible generation of primary magnesian calc-alkalic andesite magmas by direct partial melting of the upper mantle peridotite under hydrous conditions at depths between 40 and 60 km.     

Petrogenetic modeling of rock variety in the Khalkhab–Neshveh pluton,NW of Saveh,Iran

The Khalkhab–Neshveh (KN) pluton is a part of Urumieh–Dokhtar Magmatic Arc and was intruded into a covering of basalt and andesite of Eocene to early Miocene age. It is a medium to high‐K, metaluminous and I‐type pluton ranging in composition from quartz monzogabbro, through quartz monzodiorite, granodiorite, and granite. The KN rocks show subtle differentiation trends strongly controlled by clinopyroxene, plagioclase, hornblende, apatite, and titanite, where most major elements (except K₂O) are negatively correlated with SiO₂; and Al₂O₃, Na₂O, Sr, Eu, and Y define curvilinear trends. Considering three processes of magmatic differentiation including mixing and/or mingling between basaltic and dacitic magmas, gravitational fractional crystallization and in situ crystallization revealed that the latter is the most likely process for the evolution of KN magma. This is supported by the occurrence of all rock types at the same level, the lack of mafic enclaves in the granitoid rocks, the curvilinear trends of Na₂O, Sr, and Eu, and the constant ratios of (⁸⁷Sr/⁸⁶Sr)_i from quartz monzodiorite to granite (0.70475 and 0.70471, respectively). In situ crystallization took place via accumulation of plagioclase and clinopyroxene phenocrysts and concentration of these phases in the quartz monzogabbro and quartz monzodiorite at the margins of the intrusion at T ≥ 1050°C, and by filter pressing and fractionation of hornblende, plagioclase, and later biotite in the granitoids at T = ～880°C.     

Tectonic controls on magma genesis and evolution in the northwestern United States

Field, chronologic, chemical, and isotopic data for late Cenozoic basaltic rocks from the northwestern United States illustrate the relationship between crustal structure and tectonic forces in controlling the genesis and evolution of continental volcanism. In the northwestern U.S., the first major episode of basaltic volcanism was triggered by crustal rifting in a “back-arc” environment, east of the westward-migrating volcanic arc created by the subduction of the Juan-de-Fuca plate beneath the North American plate. Rifting and volcanism were concentrated by pre-existing zones of crustal weakness associated with boundaries between the old Archean core of the continent and newly accreted terranes. Basalts erupted during this time (Columbia River, Steens Mountain) show evidence of significant fractionation histories including contamination by crust of varying age depending on the crustal structure at the eruption site. Presumably this reflects ponding and stagnation of primary magmas in the crust or at the crust-mantle interface due to their encounter with thick crust, not yet extended and still containing its low-density, easily fusible component. Continued rifting of this crust, and modification of its composition through extraction of rhyolitic partial melts and deposition of the fractionation products from primary basaltic melts, coupled with a shift in stress orientation roughly 10.5 Ma ago, allowed relatively unfractionated and uncontaminated magmas to begin reaching the surface. In the western part of the region (Oregon Plateau), these magmas tapped a mantle source similar to that which produced most of the ocean island basalts of the northern hemisphere. To the east (Snake River Plain), however, the mantle sampled by basaltic volcanism has isotopic characteristics suggesting it has preserved a record of incompatible element enrichment processes associated with the formation of the overlying Archean crustal section some 2.6 Ga ago.     

Evidence of magma mixing: Petrological study of Shirouma-Oike calc-alkaline andesite volcano, Japan

Shirouma-Oike volcano, a Quaternary composite volcano in central Japan, consists mostly of calc-alkaline andesitic lavas and pyroclastic rocks. Products of the earlier stage of the volcano (older group) are augite-hypersthene andesite. Hornblende crystallized during the later stage of this older group, whereas biotite and quartz crystallized in the younger group.Assemblages of phenocrysts in disequilibrium, such as magnesian olivine(Fo₃₀)/quartz, iron-rich hypersthene(En₅₅)/iron-poor augite(Wo_43.5, En_42.5, Fs_14.0), and two different types of zoning on the rim of clinopyroxene are found in a number of rocks. Detailed microprobe analyses of coexisting minerals reveal that phenocrysts belong to two distinctly different groups; one group includes magnesian olivine + augite which crystallized from a relatively high-temperature (above 1000°C) basaltic magma; the second group, which crystallized from relatively low temperature (about 800°C) dacitic to andesitic magma, includes hypersthene + hornblende + biotite + quartz + plagioclase + titanomagnetite ± ilmenite (in the younger group) and hypersthene + augite + plagioclase + titanomagnetite ± hornblende (in the older group). The temperature difference between the two magmas is clarified by Mg/Fe partition between clinopyroxene and olivine, and Fe-Ti oxides geothermometer. The compositional zoning of minerals, such as normal zoning of olivine and magnesian clinopyroxene, and reverse zoning of orthopyroxene, indicate that the basaltic and dacitic-andesitic magmas were probably mixed in a magma reservoir immediately before eruption. It is suggested that the basaltic magma was supplied intermittently from a deeper part to the shallower magma reservoir, in in which dacitic-andesitic magma had been fractionating.     

Rb–Sr and Sm–Nd isotopic studies of mafic igneous rocks from the Ryoke plutono-metamorphic belt in the Setouchi area, Southwest Japan: implications for the genesis and thermal history

Abstract Rb–Sr and Sm–Nd isochron ages were determined for whole rocks and mineral separates of hornblende‐gabbros and related metadiabases and quartz‐diorite from Shodoshima, Awashima and Kajishima islands in the Ryoke plutono‐metamorphic belt of the Setouchi area, Southwest Japan. The Rb–Sr and Sm–Nd whole‐rock‐mineral isochron ages for six samples range from 75 to 110 Ma and 200–220 Ma, respectively. The former ages are comparable with the Rb–Sr whole‐rock isochron ages reported from neighboring Ryoke granitic rocks and are thus due to thermal metamorphism caused by the granitic intrusions. On the contrary, the older ages suggest the time of formation of the gabbroic and related rocks. The initial ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios of the gabbroic rocks (0.7070–0.7078 and 0.51217–0.51231 at 210 Ma, respectively) are comparable with those of neighboring late Cretaceous granites and lower crustal granulite xenoliths from Cenozoic andesites in this region. Because the gabbroic rocks are considered to be fragments of the lower crustal materials interlayered in the granulitic lower crust, their isotopic signature has been inherited from an enriched mantle source or, less likely, acquired through interaction with the lower crustal materials. The Sr and Nd isotopic and petrologic evidence leads to a plausible conclusion that the gabbroic rocks have formed as cumulates from hydrous mafic magmas of light rare earth element‐rich (Sm/Nd < 0.233) and enriched isotopic (?_Sr > 0 and ?_Nd < 0) signature, which possibly generated around 220–200 Ma by partial melting of an upper mantle. We further conclude that they are fragments of refractory material from the lower crust caught up as xenoblocks by granitic magmas, the latter having been generated by partial melting of granulitic lower crustal material around 100 Ma.     

Content and behavior of fluorine in Japanese quaternary volcanic rocks and petrogenetic application

Fluorine contents in about 160 representative Quaternary volcanic rocks and 15 hornblende and biotite phenocrysts in a calc-alkali series in Japan have been determined by a selective ion-electrode method. Tholeiites have the lowest contents and the narrowest range (58–145 ppm), while alkali basalts have the highest contentws and the widest range (301–666 ppm), high-alumina basalts have intermediate values (188–292 ppm). F contents in basalts clearly increase from east to west across the Japanese Islands, as do alkalies, P₂O₅ REE, U, Th and H₂O.The volcanic rocks studied are divided into two groups on the basis of F: (1) witt, increasing % SiO₂ or advancing fractionation, F contents show either progressive enrichment; or (2) with increasing fractionation, F contents show rather constant values. The former is produced by fractionation of anhydrous phases from basalt to mafic andesite magmas; the tholeiite series of Nasu volcanic zone (outer zone), northeastern, Japan is a typical example. The latter group is derived through separation of amphibole-bearing phases from basaltic magmas at various depths from upper mantle (about 30 km) to upper crust; the alkali series in southwestern Japan and the calc-alkali series of Chokai volcanic zone (inner zone), northeastern Japan, are examples.     

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.     

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.     

Basalt and tonalite from the Amami Plateau, northern West Philippine Basin: New Early Cretaceous ages and geochemical results, and their petrologic and tectonic implications

Abstract Basalts and tonalites dredged from the Amami Plateau in the northern West Philippine Basin have the geochemical characteristics of intraoceanic island arc rocks: low ⁸⁷Sr/⁸⁶Sr (0.70297–0.70310), intermediate ¹⁴³Nd/¹⁴⁴Nd (0.51288–0.51292), moderate light rare earth element (LREE) enrichment (La/Yb = 4.1–6.6) and high La/Nb (1.4–4.3). The incremental heating of hornblende from tonalites yielded well‐defined plateaus and ⁴⁰Ar/³⁹Ar isochron ages of 115.8 ± 0.5 Ma and 117.0 ± 1.1 Ma, while plagioclase yielded disturbed Ar release patterns, with ages ranging from 70 to 112 Ma. Taken together, these results show that the Amami Plateau was formed by subduction‐related magmatism in the Early Cretaceous period, earlier than indicated by prior K/Ar results. The results support tectonic models in which the West Philippine Basin was opened within a complex of Jurassic–Paleocene island arc terranes, which are now scattered in the northern West Philippine Basin, the Philippine Islands and Halmahera. The Amami Plateau tonalites and basalts have higher Sr/Y and lower Y and ⁸⁷Sr/⁸⁶Sr compared with younger tonalitic rocks from the northern Kyushu–Palau Ridge and the Tanzawa complex, which were formed by the subduction of the Pacific Plate beneath the Philippine Sea Plate. Based on the geochemical characteristics of the basalts, the Early Cretaceous subduction zone that formed the Amami Plateau may have been the site of slab melting, which suggests that a younger and hotter plate was being subducted at that time. However, the Amami tonalites were probably formed from basaltic magma by fractional crystallization or by partial melting of basaltic arc crust, rather than by melting of the subducted slab.     

Rift Valley in the Atlantic Ocean near 36°50′N: petrology and geochemistry of basaltic rocks

Dredged rocks from an area of about 15 km² within the inner floor and on the adjacent walls of the Rift Valley were collected. Based on petrographic and chemical data, four types of basaltic rocks were recognized: (1) picritic basalts with olivine xenocrysts, TiO₂ < 0.6%, K₂O < 0.1%, (2) olivine basalts with olivine megacrysts, TiO₂ = 0.8–1.5%,K₂O = 0.1–0.2%, (3) highly phyric and moderately phyric plagioclase basalts with megacrystic plagioclase, TiO₂ < 1.3%, K₂O < 0.3%, and (4) pyroxene basalts with pyroxene > plagioclase, TiO₂ = 0.8–1%,K₂O = 0.2–0.4%. The Cr and Ni having high partition coefficients show different variation trends for each type of rock and their values decrease continuously as crystallization proceeds within each type of basalt. It is speculated that two different magmas have given rise to the above-mentioned rocks. One has yielded the picritic basalts and subsequently the olivine basalts after a separation of the olivine cumulates; the other gave rise to the plagioclase basalts.     

Evidence for crustal assimilation by turbulently convecting,mafic alkaline magmas: Geochemistry of mantle xenolith-bearing lavas from northern Sardinia

Alkali basalt, trachybasalt and basanite magmas, containing abundant xenoliths of upper mantle origin, were erupted during the Plio-Pleistocene (2.4-0.14 Ma) in northern Sardinia. The magmas are enriched in K, Rb, Th and Ba relative to mid-ocean ridge basalts (MORB) and most ocean island basalts (OIB), resulting in high K/Nb, Th/Nb, Ba/Nb and Rb/Nb ratios. The large number of spinel peridotite inclusions in these lavas suggests that these chemical features cannot be explained by combined assimilation and fractional crystallization within the continental crust. However, volcanic rock chemistry can be explained by the assimilation of sialic rocks by turbulently convecting, mafic magmas during their ascent to the surface. Fractionation of Ba and K from the light rare earth elements (LREE) is required to explain the positive correlation of K/La and Ba/La with ⁸⁷Sr/⁸⁶Sr_(i). Consequently, bulk assimilation of crystalline basement rocks by rising, hot basaltic magmas cannot explain the observed chemical trends, and preferential melting of a low melting quartzo-feldspathic crustal component probably occurred, leaving the REE in residual phases such as apatite, zircon, sphene and amphibole. Alternatively, large ion lithophile element (LILE) enrichment may have been related to interaction of rising mafic lavas with metasomatized lithospheric mantle or enriched asthenosphere.     

Gabbroic xenoliths from La Palma, Tenerife and Lanzarote, Canary Islands: evidence for reactions between mafic alkaline Canary Islands melts and old oceanic crust

Gabbroic and hornblendite xenoliths from La Palma, Tenerife and Lanzarote fall into three main groups based on petrography and chemistry. One group (comprising all xenoliths from Lanzarote and some from La Palma) consists of highly deformed orthopyroxene-bearing gabbroic rocks that show a strong affinity to N-MORB and oceanic gabbro cumulates in terms of mineral chemistry and REE relations. However, they show mild enrichment in the most incompatible elements (particularly Rb+Ba±K) relative to intermediate and heavy REE, and their Sr–Nd isotope ratios fall within or close to the N-MORB field. The second group (60% of the xenoliths from La Palma) are gabbroic cumulates with zoned clinopyroxenes (Ti–Al-poor cores, Ti–Al-rich rims) and reaction rims of hornblende, biotite and clinopyroxene on other phases. Their trace-element and Sr–Nd isotope relations are in general transitional between N-MORB cumulates and Canary Islands alkali basalts, but they show strong enrichment in Rb, Ba and K relative to other strongly incompatible elements. The third group (comprising some xenoliths from La Palma and all those from Tenerife) are undeformed gabbroic and hornblendite rocks in which hornblende and biotite appear to belong to the primary assemblage. These rocks show strong affinities to Canary Islands alkali basaltic magmas with respect to mineral, trace-element, and Sr–Nd isotope chemistry. The first two groups are interpreted as fragments of old oceanic crust which have been mildly to strongly metasomatized through reactions with Canary Islands alkaline magmas. The reaction process is a combination of enrichment in elements compatible with biotite (and hornblende), and simple mixing between N-MORB cumulates and trapped alkaline magmas. The third group represents intrusions/cumulates formed from mafic alkaline Canary Islands magmas. Modeling indicates that locally up to 50% new material has been added to the old oceanic crust through reactions with ocean island basalts. Reactions and formation of cumulates do not represent simple underplating at the mantle/crust boundary, but have taken place within the pre-existing oceanic crust, and are likely to have significantly thickened the old oceanic crust.     

Adakitic lavas in the Central Luzon back‐arc region,Philippines: lower crust partial melting products?

Abstract Volcanism in the back-arc side region of Central Luzon, Philippines, with respect to the Manila Trench is characterized by fewer and smaller volume volcanic centers compared to the adjacent forearc side-main volcanic arc igneous rocks. The back-arc side volcanic rocks which include basalts, basaltic andesites, andesites and dacites also contain more hydrous minerals (ie, hornblende and biotite). Adakite-like geochemical characteristics of these back-arc lavas, including elevated Sr, depleted heavy rare earth elements and high Sr/Y ratios, are unlikely to have formed by slab melting, be related to incipient subduction, slab window magmatism or plagioclase accumulation. Field and geochemical evidence show that these adakitic lavas were most probably formed by the partial melting of a garnet-bearing amphibolitic lower crust. Adakitic lavas are not necessarily arc–trench gap region slab melts.