Calc-alkaline volcanic rocks from NW Sardinia: Evaluation of a fractional crystallization model

The volcanic centre of Monte Seda Oro, N. W. Sardinia, representative of a Cenozoic calc-alkaline andesitic suite of rocks is composed of a variety of rocks ranging from high alumina basalts to dacites. The minerals of basaltic, andesitic and dacitic rocks show only limited variation in chemical composition. The geochemical data suggest that the various rock-types are related by a crystal-liquid fractionation. Least-squate numerical calculations, using major element data, support the derivation of andesites with SiO₃ content ranging from 53.8 to 59.0% from basalts having about 48.7% of SiO₂ by low pressure crystal fractionation of the phenocryst phases present in these rocks. However, the origin of dacites cannot be readily explained by this mechanism.     

Petrochemical affinities of volcanic rocks from the tonga — Kermadec island arc,Southwest Pacific

Eruptive suites from Tonga (tholeiitic), Raoul Island (tholeiitic) and Macauley Island (high-alumina) are characterised by low alkalis, an absence of andesites in the range 56–65% silica, and restricted acidity for minor glassy differentiates (SiO₂=65–68 %). These volcanics form a chain of islands overlying a seismic zone which extends from Tonga to the central volcanic region of North Island, New Zealand where a calc-alkaline series contains basaltic, andesitic and rhyolitic members in that order of increasing abundance. Within this continental suite, tholeiitic and high-alumina phases are recognised as closely similar to the intra-oceanic Tonga-Kermadec magma types and show petrochemical gradation into the medium-silica andesites, apparently by sialic assimilation.     

Petrology of tholeiitic lavas from Tanna Island (New Hebrides): Importance of cumulative processes in Island arc magmatism

Tanna, one of the southernmost islands of the New Hebrides volcanic arc, is made of Late Pliocene to Recent island arc tholeiitic basalts and andesites, with SiO₂ contents ranging from 45 to 57%. These lavas are highly porphyritic (30–50% in volume): phenocrysts of plagioclase are the most abundant, together with olivine and clinopyroxene. The groundmass contain plagioclase, augite, olivine, magnetite and glass; pigeonite, tridymite, sanidine and, rarely, biotite may also occur. The olivines and clinopyroxenes show an iron enrichment from the cores of phenocrysts to their rims and the groundmass crystals, but their compositional variations are not correlated with the Mg/Fe ratio of bulk host rocks, the most Fe-rich compositions being found in Mg-rich lavas. Plagioclase compositions range from An₉₅ to An₆₀ in the basalts and An₆₀ to An₅₀ in the andesites, but, within each group, they are not correlated with SiO₂ or Na₂O contents of host lavas. Consequently, the bulk major element compositions of Tanna volcanic rocks cannot be considered as primarily controlled by crystal separation from successive liquids. The oxyde-SiO₂ variations diagrams, and the modal compositions and mineral chemistry show that crystal accumulation is the predominant mechanism accounting for bulk rock compositions. However, this does not exclude fractional crystallization: the variation of the calculated groundmass mineralogy strongly suggest the occurrence of crystal removal mainly clinopyroxene and magnetite.     

The composition and differentiation of the volcanic rocks of Carriacou,grenadines, West Indies

Tertiary volcanic rocks of Carriacou occupy two-thirds of the island. The volcanics include volcaniclastics, lava flows and dome lavas and range in composition from basalts to andesites. Carriacou basalts fall into two petrographic types (a) clinopyroxene-plagioclase-phyric basalts and (b) olivine microphyric basalts; the latter having higher MgO and lower Al₂O₃ than the clinopyroxene basalts. Both types are unusually rich in mafic minerals compared with Lesser Antilles basalts in general, although similar types have been reported from the nearby island of Grenada. The potash to silica ratios are relatively high and confirm the similarity between Carriacou and Grenada basalts and the differences between these basalts and basalts from other islands of the Lesser Antilles. The basaltic andesites and andesites from Carriacou correspond closely in mineralogical and chemical composition with typical andesites found elsewhere in the Lesser Antilles. The geochemistry of the volcanics shows that the olivine microphyric basalts display tholeiitic affinities whereas the clinopyroxeneplagioclase-phyric basalt, basaltic andesites and andesites are calcalkaline. The compositional gradation in both the geochemistry and mineralogy of these volcanics suggests that fractional crystallization played an important role in the derivation of the various magma.     

Boninite as a possible calc-alkalic primary magma

Boninite is an unusual, plagioclase-free magnesian andesite, occurring as vesicular pillow lavas and hyaloclastites, accompanied by andesites and dacites in Chichi-jima, Bonin Islands. The Bonin Islands belong to the Izu-Mariana arc and consist of dominant volcanic rocks and subordinate sedimentary rocks of late Oligocene-early Miocene age. The chemistry of boninite is characterized by high contents of MgO. Cr and Ni similar to primitive basalts, but apparently in ill accord with its relatively high SiO₂ content of ? 55%. The relation of SiO₂ to total FeO/MgO ratio indicates that boninite belongs to the cale-alkalic rock suite. The mineralogy of boninite consists of olivine (Fo87-90), orthopyroxene (En87-90), clinopyroxene (Wo38-35En37-44Fs25-21), hydrous glass and Cr-spinel, Experimental studies show that the magma of boninite composition could be in equilibrium with upper mantle peridotite at pressures less than 17 kb and temperatures of 1200–1050°C under high P_H2_O. It is suggested that boninite is a sea-floor quenched product (900°C) of a direct partial melt of the upper mantle. Related andesites and dacites are considered to be probably fractional crystallization products from the same magma.     

Geochemistry of the volcanics of central Mexico

The Tertiary and Recent volcanics of Mexico occur in two provinces. The Cordillera Province is made up of about 1700 m of ignimbrite sheets overlain and intercalated in the upper part by olivine basalt and basaltic andesite. The Rio Lerma Province extends transversely across Mexico and in the Valley of Mexico the lavas consist mainly of andesite and dacite, 68 % of those analysed having 62 | 4.7 % SiO₂. A total of 108 chemical analyses were made for the major elements, 90 of these including determinations of Cr, Ni, Cu, Zn, Rb, Sr, Ba, Th and Pb for two areas, the Valley of Mexico in the Rio Lerma Province and the Guadalajara region which lies at the intersection of the two provinces. Computer constructions of normative components in the basalt tetrahedron and other projections support an origin of partial melting of tholeiitic to pyrolitic material for the production of andesite. The Guadalajara lavas have consistently higher K/SiO₂ and K/Rb ratios and lower Mg/SiO₂ ratio than the Valley of Mexico rocks suggesting generation at greater depth.     

Agrigan: An introduction to the geology of an active volcano in the Northern Mariana Island arc

Agrigan is the tallest (965 m a.s.l.) and largest (44 km²) of the volcanoes of the northern Mariana Islands. Its slopes are asymmetric to the east; a small caldera (4 km²) dominates the interior. The volcanic edifice has been disrupted along three sets of faults: 1) exterior slump faults, 2) radial faults, and 3) interior faults related to caldera-collapse. The rocks of the volcano are characterized by porphyritic clinopyroxene-olivine-plagioclase basalts and subordinate andesites. Cumulate xenoliths composed of Fo₈₁, An₉₅ and diopside are common in the basalts. Development of the volcano began with 3–4 km of submarine growth. The earliest recognizable flows are the result of fissural Hawaiian- and Strombolian-type eruptions. These were followed by the eruption of more viscous lavas from above the present summit. Flank eruptions of basalt and andesite preceded voluminous outpourings of andesitic pyroclastics contemporaneous with caldera-collapse. Subsequent magmatic resurgence is localized along a N10E rift zone. Violent ejection of lapilli and ash occurred in 1917.     

Volcan ceboruco: A major composite volcano of the mexican volcanic belt

Ceboruco is a major composite volcano at the western end of the Mexican Volcanic Belt, near the junction between the North American and Pacific plates. The volcano is built from successive eruptions of andesite lavas and pyroclastic rocks, and major eruptions during its history have resulted in the formation of two concentric calderas. The youngest volcanic activity has included the extrusion of dacites within the inner caldera and a voluminous flank eruption of andesite during 1870–72. Fumarolic activity persists to the present day. Chemical analyses show that the lavas are of cale-alkaline type and rangs from andesite (SiO₂=58–61%) to acid dacite (SiO₂=68%) in composition. The rate of increase of K₂O relative to SiO is greater than that in volcanic rocks from the Mexican Volcanic Belt as a whole. This indicates that simple models based on the application of such relationships may not be adequate to explain the petrogenesis of calc-alkaline lavas.     

Eruption of Piip Crater (Kamchatka)

In autumn of 1966 on the northern slope of Kliuchevskoy volcano a chain of new adventive craters broke out at the height of about 2200 m. Eighty-four hours before the beginning of the eruption a swarm of preliminary volcanic earthquakes had appeared. The number of preliminary shocks was 457 with total energy of 4 × 10¹⁷ erg. With the beginning of the lava flow the earthquakes stopped and a continuous volcanic tremor appeared. The total energy of volcanic tremor amounts to 10¹⁶ erg. During the eruption numerous explosive earthquakes with the energy of 10¹⁵–10¹⁶ erg were recorded and besides the microbarograph of the Volcanostation recorded 393 explosions with an energy more than 10¹³ erg and their total energy was equal to 10¹⁷ erg. All together it has been formed 8 explosive craters and the lowest 9th crater was effusive. The slag cone was formed round this effusive crater, the lava effusion of basaltic-andesite composition (52,5% SiO₂) tooke place from the lava boccas at the cone base and from the crater. The lava flow covered a distance of 10 km along the valley of the Sopochnoy river and descended to a height of about 800 m. The lava flow velocity at the outflow reached 800 m/hr, the lava temperature was 1050°C. The effused lava volume amounts to 0.1 km³. The eruption stopped on December 25–26, 1966.     

Fractional crystallization trends in the system Mg2SiO4-CaAl2Si2O8-FeO-Fe2O3-SiO2 over the range of oxygen partial pressures of 10−11 to 10−0.7 atm

A brief report is made of current laboratory investigations on phase relations among olivine, pyroxene, anorthite, magnetite, tridymite, liquid and gas in the system Mg₂SiO₄-CaAl₂Si₂O₈-FeO-Fe₂O₂-SiO₂ over a wide range of oxygen partial pressures. Courses of fractional crystallization under various conditions of oxygen partial pressure are depicted using an anorthite saturation diagram. Starting with a basalt-like composition in the system, fractional crystallization at a moderate oxygen partial pressure (10 atm.) results in an andesite-like residual liquid of composition 55 SiO₂, 14 iron oxide, 6 MgO, 9 CaO, 16 Al₂O₃ at a temperature of 1155°C. With fractional crystallization in a closed system, the end liquid approaches the composition of 45 SiO₂, 38 iron oxide, 6 CaO and 11 Al₂O₃, at a temperature of 1050°C and oxygen partial pressure of about 10^?12 atm. The andesitic final liquid in this system would be expected to further differentiate toward dacitic and rhyolitic compositions if alkalies and water were present in the system. On the basis of these studies, the derivation of liquids of andesitic, dacitic or rhyolitic composition from primary basalts by fractional crystallization seems entirely possible if the oxygen partial pressure is maintained at a moderate or high level.     

Magma types of volcanic rocks and continental margin of the Taiwan upper Paleozoic Geosyncline

Greenrocks are very common in the Tananao Schist of eastern Taiwan where the known fossils are of Permian in age. Fourty-four greenrock samples were chemically analysed and their magma types studied. The chemical composition of the greenrocks have marked variation common in volcanic rock series. The greater parts of the greenrocks belong to basalt and a smaller portion to basaltic andesite (SiO₂ 53 %–58 %). They are probably isochemical with their original igneous rocks except for volatile components. No striking Fe-enrichment exists in a MgO-ΣFeO-(Na₂O=K₂O) diagram. Based on (Na₂O=K₂O)-Al₂O₃-SiO₂ diagrams afterKuno (1960), the parent magma of the rocks mostly belong to the high-alumina basalt series and only a few to alkali olivine basalt series. The high-alumina basalt can be looked upon as having an incipient trend for the calc-alkaline or the hypersthene series ofKuno (1959). The average K/Rb ratio of 460, the average TiO₂ percentage of 1.5 %, and low K₂O of around 0.5 % seem to warrant a conclusion that the basaltic rocks were poured out in the upper Paleozoic eugeosyncline on an embryonic continental crust. Considering the rock association of amphibolite plus serpentine (dismembered ophiolite), meta-graywacke, metachert, crystalline limestone, metaarkose, and metabasites in the Tananao Schist, the most probable site for the eugeosyncline may been an extensional trough near the fragmented paleo-Asiatic margin.     

Volcanic rocks of the Witu Islands,Papua New Guinea: The origin of magmas above the deepest part of the New Britain Benioff zone

The Witu Islands are Quaternary volcanoes that overlie the deepest (about 300–580 km) part of the New Britain Benioff zone. The islands are about 100 km south of the transcurrent-divergent plate boundary that crosses the Bismarck Sea, and they surmount the southeastern end of the Willaumez-Manus Rise. The rocks are olivine- and quartz-normative tholeiitic basalts, low- and high-SiO₂ andesites, dacites, and rhyolites. Alkaline rocks that overlie the deep (greater than 300 km) parts of other Benioff zones have not been found in the Witu Islands. Compared to the Witu Islands rocks, those with similar SiO₂ contents from New Britain volcanoes that overlie progressively shallower parts of the Benioff zone to the south, are, for example, generally poorer in Na+K, Ti, and P, and higher in Ca and Al. There are similar progressive changes in trace-element abundances, but Zr and Nb contents are distinctly richer in Witu Islands rocks.⁸⁷Sr/⁸⁶Sr values range between 0.70311 and 0.7038, which are typical for rocks from New Britain as a whole and from other island arcs in the southwest Pacific. Two¹⁴³Nd/¹⁴⁴Nd values of 0.512211 and 0.512271, taken together with the Sr isotopic results, define a source region equivalent to those for oceanic-island basalts; there is no evidence for sea-water contamination of the sources. Perhaps the most striking feature of the Witu Islands rocks is their compositional diversity. Basalts range from olivine tholeiites similar to marginal-basin basalts from other areas, to quartz tholeiites similar in most respects to those typical of island arcs, and to incompatible-element-enriched tholeiites that are close to silica-undersaturation. Andesites on Unea Island have a strong island-arc signature, but the andesites, dacites, and rhyolite of Garove Island have some features that may be more in common with the silica-oversaturated rocks of oceanic areas. The mineralogy of Witu Islands basalts is characterised by phenocrysts of olivine (Fo_89-54), plagioclase (An_90-55) and Ca-augite. Cr-Al-rich spinels and aluminous magnetites are present as inclusions in some olivine phenocrysts. Groundmass fayalite, alkali feldspar, and dacitic to rhyolitic glasses high in K/Na are found in a few samples. In contrast to basalts from volcanoes above the shallower parts of the New Britain Benioff zone, those of the Witu Islands are characterised by rarity of low-Ca pyroxene, as phenocrysts or in the groundmass. Rocks richer in SiO₂ are characterised by the presence of orthopyroxene phenocrysts and lesser amounts of olivine. Hydrous minerals appear to be absent. Groundmass Fe-Ti oxides define crystallisation temperatures (about 800–1050°C) and oxygen fugacities (fO₂) corresponding to those of the Ni-NiO buffer, but up to two fO₂ log units above it. The suite as a whole is phenocryst-poor compared to most New Britain volcanic rocks. A significant degree of mantle heterogeneity is inferred by the chemical variability of the Witu Islands rocks. However, there are no compelling reasons in support of the interpretation that source heterogeneity is due to the effect of a slab-derived component. The cause of the heterogeneity is unclear, but may be due to mantle differentiation processes related to an anomalous tectonic setting.     

The linear relation between temperatures based on the silica content of groundwater and regional heat flow: A new heat flow map of the United States

Application of the silica geothermometer to over 70,000 non-thermal groundwaters from the United States has shown that there is a correlation between the average silica geotemperatures for a region (T SiO₂ in °C) and the known regional heat flow (q in mW m^?2) of the form: 1 $$TSiO_2 = mq + b$$ wherem andb are constants determined to be 0.67°C m² mW^?1 and 13.2°C respectively. The physical significance of ‘b’ is the mean annual air temperature. The slope ‘m’ is related to the minimum average depth to which the groundwaters may circulate. This minimum depth is estimated to be between 1.4 and 2.0 km depending on the rock type. A preliminary heat flow map based on equation (1) is presented using theT SiO₂ for new estimates of regional heat flow where conventional data are lacking. Anomalously high localT SiO₂ values indicate potential geothermal areas.     

The complex filling of alae crater,Kilauea Volcano,Hawaii

Since February 1969 Alae Crater, a 165-m-deep pit crater on the east rift of Kilauea Volcano, has been completely filled with about 18 million m³ of lava. The filling was episodic and complex. It involved 13 major periods of addition of lava to the crater, including spectacular lava falls as high as 100 m, and three major periods of draining of lava from the crater. Alae was nearly filled by August 3, 1969, largely drained during a violent ground-cracking event on August 4, 1969, and then filled to the low point on its rim on October 10, 1969. From August 1970 to May 1971, the crater acted as a reservoir for lava that entered through subsurface tubes leading from the vent fissure 150 m away. Another tube system drained the crater and carried lava as far as the sea, 11 km to the south. Much of the lava entered Alae by invading the lava lake beneath its crust and buoying the crust upward. This process, together with the overall complexity of the filling, results in a highly complicated lava lake that would doubtless be misinterpreted if found in the fossil record.     

Melting of Mg2GeO4 under pressure

Melting point of germanate forsterite, Mg₂GeO₄, was raised by compression at the rate of 30°C/GPa. The triple point, at which three phases of olivine- and spinel-type solids and liquid coexisted, was fixed at 1950°C and 3.5GPa. Wen these results are combined with the thermodynamical data of forsterite, Mg₂SiO₄, it is estimated that the triple point of forsterite lies in a region ranging from 2700° to 3000°C in temperature and from 20 to 30GPa in pressure.     

Crystallization of tholeiitic basalt in Alae Lava Lake,Hawaii

The eruption of Kilauea Volcano August 21–23, 1963, left 600,000 cubic meters of basaltic lava in a lava lake as much as 15 meters deep in Alae pit crater. Field studies of the lake began August 27 and include repeated core drilling, measurements of temperature in the crust and melt, and precise level surveys of the lake surface. The last interstitial melt in the lake solidified late in September 1964; by mid August 1965 the maximum temperature was 690°C at a depth of 11.5 meters. Pumice air-quenched from about 1140°C contains only 5 percent crystals — clinopyroxene, cuhedral olivine (Fo ₈₀), and a trace of plagioclase, (An ₇₀). Drill cores taken from the zone of crystallization in the lake show that olivine continued crystallizing to about 1070°C; below that it reacts with the melt, becoming corroded and mantled by pyroxene and plagioclase. Below 1070°C, pyroxene and plagioclase crystallized at a constant ratio. Ilmenite first appeared at about 1070°C and was joined by magnetite at about 1050°C; both increased rapidly in abundance to 1000°C. Apatite first appeared as minute needles in interstitial glass at 1000°C. Both the abundance and index of refraction of glass quenched from melt decreased nearly linearly with falling temperature. At 1070°C the quenched lava contains about 65 percent dark-brown glass with an index of 1.61; at 980°C it contains about 8 percent colorless glass with an index of 1.49. Below 980°C, the percentage of glass remained constant. Progressive crystallization forced exsolution of gases from the melt fraction; these formed vesicles and angular pores, causing expansion of the crystallizing lava and lifting the surface of the central part of the lake an average of 19.5 cm. The solidified basalt underwent pneumatolitic alteration, including deposition of cristobalite at 800°C, reddish alteration of olivine at 700°C, tarnishing of ilmenite at 550°C, deposition of anhydrite at 250°C, and deposition of native sulfur at 100°C. Ferric-ferrous ratios suggest that oxidation with maximum intensity between 550°C and 610°C moved downward in the crust as it cooled; this was followed by reduction at a temperature of about 100°C. The crystallized basalt is a homogeneous fine-grained rock containing on the average 48.3 percent by volume intergranular pyroxene (augite > pigeonite), 34.2 percent plagioclase laths (An_{60 70}), 7.9 percent interstitial glass, 6.9 percent opaques (ilmenite > magnetite), 2.7 percent olivine (Fo_{70 80}), and a trace of apatite. Chemical analyses of 18 samples, ranging from initially quenched pumice to lava cored more than a year after the eruption from the center and from near the base of the lake, show little variation from silica-saturated tholeiitic basalt containing 50.4 percent SiO₂, 2.4 percent Na₂O, and 0.54 percent K₂O. Apparently there was no significant crystal settling and no appreciable vapor-phase transport of these components during the year of crystallization. However, seven samples of interstitial liquid that had been filter-pressed into gash fractures and drill holes from partly crystalline mush near the base of the crust show large differences from the bulk composition of the solidified crust—lower MgO, CaO, and Al₂O₃; and higher total iron, TiO₂, Na₂O, K₂O, P₂O₅, and F, and, in most samples, SiO₂. The minor elements Ba, Ga, Li, Y, and Yb and possibly Cu tend to be enriched in the filter-pressed liquids, and Cr and possibly Ni tend to be depleted.     

A comparison of the recent eruptions of Mt. Pelée,Martinique and Soufrière,St. Vincent

The simultaneous eruption of Mt. Pelée, Martinique and Soufrière, St. Vincent are regarded as the first recognized examples of Pelean-type and St. Vincent-type pyroclastic eruptions. Both produced nuées ardentes, the former usually laterally directed because of the presence of a dome and the latter vertically directed from an open crater. Both volcanoes have subsequently erupted for a second time this century. The 1902–05 and 1929–32 eruptions of Mt. Pelée produced andesite lava of almost identical composition and mineralogy. Both contain two generations of plagioclase, orthopyroxene, Fe-Ti oxide, corroded brown amphibole and olivine rimmed by pyroxene. In contrast, the Soufrière material is more basic in composition varying from basaltic andesite to basalt in 1902–03 and basaltic andesite in 1971–72. The Soufrière material contains two generations of plagioclase (with those of 1971–72 having additional zones of labradorite), clinopyroxene, orthopyroxene, olivine and Fe-Ti oxide. The pyroclastic deposits are strikingly different, those from the Pelean-type eruption are termed «block and ash deposits» being characterised by poorly vesicular lava blocks up to 7 m in diameter, while the St. Vincent-type eruption produced «scoria and ash deposits» containing vesicular ropey blocks or bombs no larger than 1 m in diameter. The differences in styles of eruption are attributed to differences in viscosity and mechanism of eruption of the magmas. Stratigraphic studies of Mt. Pelée reveal that the volcano has produced basaltic andesite scoria and ash deposits from St. Vincent-type eruptions. It is concluded that the recent eruptions of Pelée tapped a deep level magma during both eruptions releasing magma of similar composition, while the 1971 Soufrière magma is thought to be a remnant of the 1903 basaltic magma which remained at a high level within the volcano where it underwent enrichment in plagioclase and loss of olivine and oxide.     

Geochemistry of upper cretaceous volcanic rocks from the pontic chain,northern turkey

Preliminary data on major elements, Cs, Ba, Rb, Pb, Sr, REE, Y, Th, U, Zr, Ht, Sn, Nb, W, Mo, Cr, V, Sc, Ni, Co and Cu contents for eight samples coming from the Upper Cretaceous volcanic belt of the Pontic Chain (Northern Turkey) are reported. SiO, versus K₂O relationship shows that the analyzed samples belong to the calc-alkaline and shoshonite series. The calc-alkaline rocks appear to represent two distinct magma types one close in composition to typical island are calc-alkaline magmas and one with high incompatible elements concentration and tractionated heavy REE patterns which suggest a genesis by partial melting at high pressure with a garnet bearing residue. Shoshonitic rocks show Na₂O/K₂O close to one, high incompatible elements concentration, and TiO₂%. Al₂O₃%, Ni and Co contents, Ni/Co and V/Ni ratios and REE patterns similar to typical island are andesites which suggest for these rocks similar genetical processes as the island are calc-alkaline magmas.     

Major-element petrochemistry of some extrusive rocks from the volcanically active Mariana Islands

Volcanic rocks from six of the currently or recently active volcances of the Mariana Island are show little variation in major element abundances. SiO₂ content averages 51.5 wt.%. The flows are high in Al₂O (mean 17.7 wt.%) and Fe oxides (mean 10.1 wt.% calculated as FeO only), and moderate in MgO content (mean 4.7 wt.%), Na₂O (mean 2.7 wt.%), and K₂O (mean 0.7 wt.%). Only the rocks from Farallon de Pajaros, the northernmost of the Mariana Islands, deviate slightly from the average of the analyses. Three analyses from this island are slightly higher in SiO₂ (about 54 wt.%) and Al₂O₃, and are lower in total Fe oxides and MgO. According to preferred classification, the lavas of the Mariana Islands can be termed mela-andesites, high-alumina basalts, or calc-alkaline (orogenic) basalts. The K₂O values (mean 0.7 wt.%) obtained from lavas of the Mariana Islands are significantly higher than the K₂O values (about 0.33 wt.%) from volcanics of the Izu chain to the north. Inasmuch as the substantial scatter in location of earthquake foci beneath both arcs prevents accurate delineation of the upper boundary of the Benioff zone, it presently cannot be determined whether this discrepancy in K₂O values reflects a difference in depth from the volcanic are to the dipping seismic zone or relates to other phenomena. The older volcanic islands within the Mariana-Bonin island chain apparently defined an island arc system during Eocene to Miocene time. This indicates that the present plane of convergence between the Pacific plate and the Philippine Sea plate has defined the convergence between these plates since Eocene time.     

Petrology of basaltic xenoliths in andesitic to dacitic host lavas from Martinique (lesser antilles): Evidence for magma mixing

Some recent calc-alkaline andesites and dacites from southern and central Martinique contain basic xenoliths belonging to two main petrographic types:

The most frequent one has a hyalodoleritic texture (« H type ») with hornblende + plagioclase + Fe-Ti oxides, set in an abundant glassy and vacuolar groundmass.

The other one exhibits a typical porphyritic basaltic texture (« B type ») and mineralogy (olivine + plagioclase + orthopyroxene + clinopyroxene + Fe-Ti oxides and scarce, or absent hornblende).

Gradual textural and mineralogical transitions occur between these two types (« I type ») with the progressive development of hornblende at the expense of olivine and pyroxenes. Mineralogical and chemical studies show no primary compositional correlations between the basaltic xenoliths and their host lavas, thus demonstrating that the former are not cognate inclusions; they are remnants of basaltic liquids intruded into andesitic to dacitic magma chambers. This interpretation is strengthened by the typical calc-alkaline basaltic composition of the xenoliths, whatever their petrographic type (« H », « I » or « B »). The intrusion of partly liquid, hot basaltic magma into colder water-saturated andesitic to dacitic bodies leads to drastic changes in physical conditions. The two components; the basaltic xenoliths are quenched and homogeneized with their host lavas with respect to T^o;fO₂ andpH₂O conditions. « H type » xenoliths represent original mostly liquid basalts in which such physical changes lead to the formation of hornblende and the development of a vacuolar and hyalodoleritic texture. The temperature increase of the acid magma depends on the amount of the intruding basalt and on the thermal contrast between the two components. The textural diversity which characterizes the xenoliths reflects the cooling rate of the basaltic fragments and/or their position relative to the basaltic bodies (chilled margins or inner, more crystallized, portions). In addition to physical equilibration (T, fO₂) between the magmas, mixing involves:

mechanical transfer of phenocrysts from one component to another, in both directions;

volatile transfer to the basaltic xenoliths, with chemical exchanges.

It is here demonstrated that a short period of time (some ten hours to a few days) separates the mixing event from the eruption, outlining the importance of magma mixing in the triggering of eruption. The common occurrence of basaltic xenoliths (generally of « H » type) in calc-alkaline lavas is emphasized, showing that this mechanism is of first importance in calc-alkaline magma petrogenesis.