Geology and geochemistry of basaltic lava flows and dikes from the Trans-Koolau tunnel, Oahu, Hawaii

A 200-m section of Koolau basalt was sampled in the 1.6-km Trans-Koolau (T–K) tunnel. The section includes 126 aa and pahoehoe lava flows, five dikes and ten thin ash units. This volcanic section and the physical characteristics of the lava flows indicate derivation from the nearby northwest rift zone of the Koolau shield. The top of the section is inferred to be 500–600 m below the pre-erosional surface of the Koolau shield. Therefore, compared with previously studied Koolau lavas, this section provides a deeper, presumably older, sampling of the shield. Shield lavas from Koolau Volcano define a geochemical end-member for Hawaiian shields. Most of the tunnel lavas have the distinctive major and trace element abundance features (e.g. relatively high SiO₂ content and Zr/Nb abundance ratio) that characterize Koolau lavas. In addition, relative to the recent shield lavas erupted at Kilauea and Mauna Loa volcanoes, most Koolau lavas have lower abundances of Sc, Y and Yb at a given MgO content; this result is consistent with a more important role for residual garnet during the partial melting processes that created Koolau shield lavas. Koolau lavas with the strongest residual garnet signature have relatively high ⁸⁷Sr/⁸⁶Sr, ¹⁸⁷Os/¹⁸⁸Os, ¹⁸O/¹⁶O, and low ¹⁴³Nd/¹⁴⁴Nd. These isotopic characteristics have been previously interpreted to reflect a source component of recycled oceanic crust that was recrystallized to garnet pyroxenite. This component also has high La/Nb and relatively low ²⁰⁶Pb/²⁰⁴Pb, geochemical characteristics which are attributed to ancient pelagic sediment in the recycled crust. Although most Koolau lavas define a geochemical endmember for Hawaiian shield lavas, there is considerable intrashield geochemical variability that is inferred to reflect source characteristics. The oldest T–K tunnel lava flow is an example. It has the lowest ⁸⁷Sr/⁸⁶Sr, Zr/Nb and La/Nb, and the highest ¹⁴³Nd/¹⁴⁴Nd ratio found in Koolau lavas. In most respects it is similar to lavas from Kilauea Volcano. Therefore, the geochemical characteristics of the Koolau shield, which define an end member for Hawaiian shields, reflect an important role for recycled oceanic crust, but the proportion of this crust in the source varied during growth of the Koolau shield. Received: 1 June 1998 / Accepted: 30 August 1998     

Magma-reservoir crystallization processes: small-scale dikes in cumulate gabbros, Mauna Kea Volcano, Hawaii

 Gabbroic xenoliths that represent cumulate environments within Mauna Kea Volcano are, in rare examples, penetrated by small-scale (<7 cm) dikes. We examined four dike/host composite xenoliths to establish how this evidence for magma seemingly injected into cumulate gabbro fits into the evolution of igneous processes in shield volcano magma reservoirs. Olivine, clinopyroxene, and plagioclase compositions in both host gabbros and dikes are characteristically tholeiitic and evolved (Fo_71–66, cpx-Mg # 79–77, An_72–51) with respect to Hawaiian magmatism. Dikes, however, when compared with their host gabbros, have slightly greater abundances of some incompatible elements and slightly more evolved olivine compositions (e.g., Fo₆₈ vs Fo₇₁₎. Compared with Mauna Kea lava compositions, both host gabbros and dikes have lower incompatible-element abundances, positive Eu anomalies, and, notable for dikes, major-element compositions unlike those of lavas (e.g., SiO₂<46 wt.%). The small-scale dikes, therefore, also have cumulate characteristics. We interpret them as representing late-stage liquids (e.g., <5 wt.% MgO, based on <Fo₇₀) "squeezed" from solidifying cumulus piles of evolved (e.g., ∼Fo₇₀) gabbroic assemblages. The compositions of the dikes, however, do not match those of the most evolved liquids expected in reservoirs because they appear to have lost interstitial liquids (e.g., positive Eu anomalies, low abundances of some trace elements). Because minerals in the dikes were in equilibrium with highly evolved liquids, conditions for small-scale dike formation in cumulate environments apparently occur only at the last stages of reservoir magma differentiation and solidification. Received: 25 February 1997 / Accepted: 14 June 1997     

Petrology of gabbroic xenoliths in 1960 Kilauea basalt: crystalline remnants of prior (1955) magmatism

The 1960 Kapoho lavas of Kilauea’s east rift zone contain 1–10 cm xenoliths of olivine gabbro, olivine gabbro-norite, and gabbro norite. Textures are poikilitic (ol+sp+cpx in pl) and intergranular (cpx+pl±ol±opx). Poikilitic xenoliths, which we interpret as cumulates, have the most primitive mineral compositions, Fo_82.5, cpx Mg# 86.5, and An_80.5. Many granular xenoliths (ol and noritic gabbro) contain abundant vesicular glass that gives them intersertal, hyaloophitic, and overall ‘open’ textures to suggest that they represent ‘mush’ and ‘crust’ of a magma crystallization environment. Their phase compositions are more evolved (Fo_80–70, cpx Mg# 82–75, and An_73–63) than those of the poikilitic xenoliths. Associated glass is basaltic, but evolved (MgO 5 wt%; TiO₂ 3.7–5.8 wt%). The gabbroic xenolith mineral compositions fit existing fractional crystallization models that relate the origins of various Kilauea lavas to one another. FeO/MgO crystal–liquid partitioning is consistent with the poikilitic ol-gabbro assemblage forming as a crystallization product from Kilauea summit magma with ∼8 wt% MgO that was parental to evolved lavas on the east rift zone. For example, least squares calculations link summit magmas to early 1955 rift-zone lavas (∼5 wt% MgO) through ∼28–34% crystallization of the ol+sp+cpx+pl that comprise the poikilitic ol-gabbros. The other ol-gabbro assemblages and the olivine gabbro-norite assemblages crystallized from evolved liquids, such as represented by the early 1955 and late 1955 lavas (∼6.5 wt% MgO) of the east rift zone. The eruption of 1960 Kapoho magmas, then, scoured the rift-zone reservoir system to entrain portions of cumulate and solidification zones that had coated reservoir margins during crystallization of prior east rift-zone magmas. Received: January 7, 1993/Accepted: November 23, 1993     

Petrology of the hilina formation,Kilauea volcano,Hawaii

The Hilina Formation comprises the oldest sequence of lava flows and tuffs exposed on Kilauea Volcano. These rocks are only exposed in kipukas in younger Puna Formation lavas along cliffs on the south flank of Kilauea Volcano. Locally, tuffs and flows of the Pahala Formation separate the underlying Hilina Formation rocks rom the overlying Puna Formation rocks. Charcoal collected from the base of the Pahala Formation yielded a C¹⁴ age of 22.800±340 years B.P. which defines a minimum age for the Hilina Formation. Hilina Formation lavas crop out over a wide region and probably originated from the summit area and from both rift zones. The Hilina Formation contains both olivine-controlled and differentiated lavas (using the terminology ofWright, 1971). The olivine-controlled lavas of the Hilina Formation are distinguishable mineralogically and geochemically from younger olivine-controlled Kilauea lavas. The younger lavas generally contain discrete low-calcium pyroxene grains. greater glass contents, higher K₂O/P₂O₅ ratios and lower total iron contents. Similar geochemical trends prevail for Manuna Loa lavas, and may typify the early lavas of Hawaiian shield volcanoes. Despite these similarities, the Hilina Formation (and all Kilauea) lavas have higher TiO₂ and CaO, and lower SiO₂ and Al₂O₃ contents than Mauna Loa Lavas. These differences have existed for over 30,000 years. Therefore, it is unlikely that the older lavas of Kilauea are compositionally similar to recent Mauna Loa lavas as was previously suggested. K₂O, TiO₂, Na₂ and Zr contents of lavas from a stratigraphic sequence of Hilina Formation lavas are variable. These variations may be utilized to subdivide the sequence into geochemical groups. These groups are not magma batches. Rather, they represent lavas from batches whose compositions may have been modified by crystal fractionation and magma mixing.     

Petrology of ultramafic and mafic xenoliths in picrite of Kahoolawe Island,Hawaii

A picrite lava (22 wt% MgO; 35 vol.% ol) along the western shore of the1.3–1.4 Ma Kahoolawe tholeiitic shield, Hawaii, contains small xenoliths of harzburgite, lherzolite, norite, and wehrlite. The various rock types have textures where either orthopyroxene, clinopyroxene, or plagioclase is in a poikilitic relationship with olivine. The Mg#s of the olivine, orthopyroxene, and clinopyroxene in this xenolith suite range between 86 and 82; spinel Mg#s range from 60 to 49, and plagioclase is An_75–80. A ⁸⁷Sr/⁸⁶Sr ratio for one ol-norite xenolith is 0.70444. In comparison, the host picrite has olivine phenocrysts with an average Mg# of 86.2 (range 87.5–84.5), and a whole-rock ⁸⁷Sr/⁸⁶Sr ratio of 0.70426. Textural and isotopic information together with mineral compositions indicate that the xenoliths are related to Kahoolawe tholeiitic magmatism, but are not crystallization products of the magma represented by their host picrite. Rather, the xenoliths are crystalline products of earlier primitive liquids (FeO/MgO ranging 1 to 1.3) at 5–9 kbar in the cumulate environment of a magma reservoir or conduit system. The presence of ultramafic xenoliths in picrite but not in typical Kahoolawe tholeiitic lava (6–9 wt% MgO) is consistent with replenishment of reservoirs by dense Mg-rich magma emplaced beneath resident, less dense tholeiitic magma. Mg-rich magmas have proximity to reservoir cumulate zones and are therefore more likely than fractionated residual liquids to entrain fragments of cumulate rock.     

Thermal areas on Kilauea and Mauna Loa Volcanoes, Hawaii

Active thermal areas are concentrated in three areas on Mauna Loa and three areas on Kilauea. High-temperature fumaroles (115–362° C) on Mauna Loa are restricted to the summit caldera, whereas high-temperature fumaroles on Kilauea are found in the upper East Rift Zone (Mauna Ulu summit fumaroles, 562° C), middle East Rift Zone (1977 eruptive fissure fumaroles), and in the summit caldera. Solfataric activity that has continued for several decades occurs along border faults of Kilauea caldera and at Sulphur Cone on the southwest rift zone of Mauna Loa. Solfataras that are only a few years old occur along recently active eruptive fissures in the summit caldera and along the rift zones of Kilauea. Steam vents and hot-air cracks also occur at the edges of cooling lava ponds, on the summits of lava shields, along faults and graben fractures, and in diffuse patches that may reflect shallow magmatic intrusions.     

Hawaiian magma-reservoir processes as inferred from the petrology of gabbro xenoliths in basalt,Kahoolawe Island

Gabbro xenoliths in a tholeiitic lava of Kahoolawe Island, Hawaii, a 1.3–1.4 Ma shield volcano, are 1–3 cm in size and comprised of plagioclase, clinopyroxene, and orthopyroxene. Gabbro textures — while intergranular and in part subophitic-are open due to 28–48 vol.% of vesicular basalt occupying xenolith space. Vesicles in and around the xenoliths are lined or filled with rhyolitic glass (segregation vesicles). The host is evolved tholeiite (MgO 6.1 wt%) with phenocrysts, microphenocrysts, and glomerocrysts of olivine, clinopyroxene, orthopyroxene, and plagioclase, and megacrysts (1 cm) of plagioclase. The Sr-isotope ratio of one xenolith is 0.70489; the host basalt ratio is 0.70460. Xenolith isotope composition, grain resorption, and clinopyroxene (Fs_12.5–15Wo_38–35.5), orthopyroxene (Fs_19.5–24Wo_4.1), and plagioclase (An_68–65Or_0.8–1.2) compositions suggest that these gabbros crystallized from Kahoolawe tholeiitic magma of essentially the same composition as the host basalt, but pre-dating the magma represented by the host. Based on the absence of intergranular Fe–Ti oxide phases from the pl+cpx+opx assemblages, and the open, vuggy textures, we envision crystallization on a reservoir roof at temperatures >1100°C. Entrainment of gabbro assemblages and plagioclase megacrysts from a roof mush/suspension zone occurred during convection associated with replenishment of the magma reservoir. These open-textured gabbro xenoliths are therefore not fragments of preexisting coarse-grained bodies such as sills or segregation veins. Rhyolitic glass in vesicles represents a gas-effervescence filtration process that forced fractionated residual liquids from the groundmass into voids associated with the xenoliths.Sirrine Environmental Consultants, Fremont, CA 94538     

Origin of differentiated lavas at Kilauea Volcano,Hawaii: Implications from the 1955 eruption

Kilauea's 1955 eruption was the first major eruption (longer than 2 days) on its east rift zone in 115 years. It lasted 88 days during which 108 × 10⁶ m³ of lava was erupted along a discontinuous, 15-km-long system of fissures. A wide compositional range of lavas was erupted including the most differentiated lavas (5.0 wt% MgO) from a historic Kilauea eruption. Lavas from the first half of the eruption are strongly differentiated (5.0–5.7 wt% MgO); later lavas are weakly to moderately differentiated (6.2–6.7 wt% MgO). Previous studies using only major-element compositions invoked either crystal fractionation (Macdonald and Eaton 1964) or magma mixing (Wright and Fiske 1971) as models to explain the wide compositional variation in the lavas. To further evaluate these models detailed petrographic, mineralogical, and whole-rock, major, and trace element XRF analyses were made of the 1955 lavas. Plagioclase and clinopyroxene in the early and late lavas show no petrographic evidence for magma mixing. Olivines from both the early and late lavas show minor resorption, which is typical of tholeiitic lavas with low MgO contents. Core-to-rim microprobe analyses across olivine, augite, and plagioclase mineral grains give no evidence of disequilibrium features related to mixing. Instead, plots of An/Ab vs distance from the core (D) and %Fo vs (D)^4.5 generated essentially linear trends indicative of simple crystal fractionation. Least-squares, mass-balance calculations for major- and trace-element data using observed mineral compositions yield excellent results for crystal fractionation (sum of residuals squared <0.01 for major elements, and <5% for trace elements); magma mixing produced less satisfactory results especially for Cr. Furthermore, trace-element plots of Zr vs Sr, Cr, and A1₂O₃ generate curved trends indicative of crystal fractionation processes. There is no evidence that mixing occurred in the 1955 lavas. Instead, the data are best explained by crystal fractionation involving a reservoir that extends at least 15 km along Kilauea's east rift zone. A dike was intruded into the rift zone from the summit reservoir eight days after the eruption started. Instead of causing magma mixing, the dike probably acted as a hydraulic plunger forcing more of the stored magma to be erupted.     

Differentiation and magma mixing on Kilauea's east rift zone

The lavas of the 1955 east rift eruption of Kilauea Volcano have been the object of considerable petrologic interest for two reasons. First, the early 1955 lavas are among the most differentiated ever erupted at Kilauea, and second, the petrographic character and chemical composition of the lava being erupted changed significantly during the eruption. This shift, from more differentiated (MgO=5.0–5.7%) to more magnesian (MgO=6.2–6.8%) lava, has been variously interpreted, as either due to systematic excavation of a zoned, differentiated magma body, or to invasion of the differentiated magma by more primitive magma, followed by rapid mixing and eruption of the resulting hybrid magmas. Petrologic examination of several nearvent spatter samples of the late 1955 lavas shows abundant evidence for magma mixing, including resorbed and/or reversely zoned crystals of olivine, augite and plagioclase. In addition, the compositional ranges of olivine, plagioclase and groundmass sulfide are very large, implying that the assemblages are hybrid. Core compositions of olivine phenocrysts range from Fo85 to Fo77. The most magnesian olivines in these samples must have originally crystallized from a melt containing 8.0–8.5% MgO, which is distinctly more magnesian than the bulk composition of the late 1955 lavas. The majorelement and trace-element data are either permissive or supportive of a hybrid origin for the late 1955 lavas. In particular, the compositional trends of the 1955 lavas on plots of CaO vs MgO, and the virtual invariance of Al₂O₃ and Sr in these plagioclase-phyric lavas are more easily explained by magma mixing than by fractionation. The pattern of internal disequilibrium/re-equilibration in the late 1955 spatter samples is consistent with reintrusion and mixing having occurred at least twice, during the latter part of the 1955 eruption. Plagioclase zonation preserves possible evidence for additional, earlier reintrusion events. Least-squares modelling the mixing of early 1955 bulk compositions with various summit lavas±olivine pick the 1952 summit lava as most like the primitive component. The results also indicate the primitive component had MgO=7.5–8.0%, corresponding to liquidus temperatures of 1165–1175°C. The absence of Fe-Ti oxide phenocrysts in the late 1955 lavas implies that the cooler component of the hybrid had T>1110°C. Thus the thermal contrast between the two components may have been as much as 55–65°C, sufficient to produce the conspicuous disequilibrium effects visible in the spatter samples.     

Pahoehoe and aa in Hawaii: volumetric flow rate controls the lava structure

The historical records of Kilauea and Mauna Loa volcanoes reveal that the rough-surfaced variety of basalt lava called aa forms when lava flows at a high volumetric rate (>5–10 m³/s), and the smooth-surfaced variety called pahoehoe forms at a low volumetric rate (<5–10 m³/s). This relationship is well illustrated by the 1983–1990 and 1969–1974 eruptions of Kilauea and the recent eruptions of Mauna Loa. It is also illustrated by the eruptions that produced the remarkable paired flows of Mauna Loa, in which aa formed during an initial short period of high discharge rate (associated with high fountaining) and was followed by the eruption of pahoehoe over a sustained period at a low discharge rate (with little or no fountaining). The finest examples of paired lava flows are those of 1859 and 1880–1881. We attribute aa formation to rapid and concentrated flow in open channels. There, rapid heat loss causes an increase in viscosity to a threshold value (that varies depending on the actual flow velocity) at which, when surface crust is torn by differential flow, the underlying lava is unable to move sufficiently fast to heal the tear. We attribute pahoehoe formation to the flowage of lava at a low volumetric rate, commonly in tubes that minimize heat loss. Flow units of pahoehoe are small (usually <1 m thick), move slowly, develop a chilled skin, and become virtually static before the viscosity has risen, to the threshold value. We infer that the high-discharge-rate eruptions that generate aa flows result from the rapid emptying of major or subsidiary magma chambers. Rapid near-surface vesiculation of gas-rich magma leads to eruptions with high discharge rates, high lava fountains, and fast-moving channelized flows. We also infer that long periods of sustained flow at a low discharge rate, which favor pahoehoe, result from the development of a free and unimpeded pathway from the deep plumbing system of the volcano and the separation of gases from the magma before eruption. Achievement of this condition requires one or more episodes of rapid magma excursion through the rift zone to establish a stable magma pathway.     

Hawaiian double volcanic chain triggered by an episodic involvement of recycled material: Constraints from temporal Sr–Nd–Hf–Pb isotopic trend of the Loa-type volcanoes

The two parallel loci of recent Hawaiian volcanoes, Kea and Loa, have been regarded as the best targets to interpret the chemical structure of an upwelling mantle plume derived from the lower mantle. Here we show that the Sr–Nd–Hf–Pb isotopic data of the shield-building lavas along the Loa locus form a systematic trend from the main shield stage of Koolau (> 2.9 Ma) to the active Loihi volcanoes. During the growth of the Koolau volcano, the dominant material in the melting region successively changed from the proposed KEA, DMK (depleted Makapuu), to EMK (enriched Makapuu) components. The proportion of EMK, dominated by a recycled mafic component, is typified by some Koolau Makapuu-stage and some Lanai lavas. Subsequently, the EMK component decreased and LOIHI component increased toward the Loihi lavas. The temporal coincidence between the episodically elevated magma production rate and the abrupt appearance of the typical Loa-type lavas that is restricted to the last 3 Myr should be linked to magma genesis. We suggest that the abrupt appearance of Loa-type magmatism should be attributed to the transient incorporation of the relatively dense recycled material and surrounding less degassed lower mantle material that accumulated near the core–mantle boundary into the upwelling plume. This episodic involvement could have been trigged by episodic thermal pulses and buoyancy increases in the plume. The continuous appearance of Kea-type lavas during the long history of Hawaiian-chain magmatism and the larger magma volume of Kea-type lavas relative to that of the Loa-type lavas in the last 3 Myr indicate that the Kea locus is closer to the thermal centre of the Hawaiian plume relative to that of the Loa locus.     

Life-time of a stratified magma chamber recorded in ultramafic xenoliths from Ichinomegata volcano,northeastern Japan

Variations in major-element chemistry and modal compositions of the mantle xenolith-bearing calc-alkalic ejecta from Ichinomegata volcano are inferred to be due to mixing of three magmatic end members: Basalt I (SiO₂ 51 wt% , MgO 8.5 wt%), Basalt II (SiO₂ 54 wt%, MgO 5 wt%), and Dacite (SiO₂ 65 wt%, MgO₂ wt%). Ultramafic xenoliths are found in mafic mixtures of Dacite-Basalt I and Dacite-Basalt II. The thermal histories of the xenoliths in both mixtures are compared with each other. Chemical compositions of olivine and orthopyroxene in xenoliths suggest that xenoliths in Basalt I were equilibrated at about 800 °C, while those in Basalt II were also equilibrated originally at about 800 °C but were subsequently annealed at about 1000 °C for more than 10^2–3 years prior to the eruption.The chemical composition of Basalt I indicates that it can coexist with upper mantle peridotite and it is an appropriate candidate for a carrier of ultramafic xenoliths from the upper mantle. On the other hand, Basalt II is fractionated and it cannot be directly derived from the upper mantle. Two pulses of xenolith-bearing basalt injection into a dacite magma chamber are inferred to have occurred. The first injection did not lead to eruption and subsequently formed a dacite/basalt stratified magma chamber. In the lower layer, the basalt was slightly differentiated to become Basalt II and ultramafic xenoliths carried by the first pulse were annealed at the bottom of the layer. The duration of the annealing of the xenoliths implies a minimum life-time of the Dacite-Basalt II stratification in the magma chamber beneath Ichinomegata of 10^2–3 years. The second injection of the xenolith-bearing basalt (Basalt I) was immediately followed by eruption, and all the magmas were effused with mixing in a conduit. Consequently, the ultramafic xenoliths carried by the second pulse are not annealed.     

The Ninole Basalt — Implications for the structural evolution of Mauna Loa volcano, Hawaii

Lava flows of the Ninole Basalt, the oldest rocks exposed on the south side of the island of Hawaii, provide age and compositional constraints on the evolution of Mauna Loa volcano and the southeastward age progression of Hawaiian volcanism. Although the tholeiitic Ninole Basalt differs from historic lavas of Mauna Loa volcano in most major-element contents (e.g., variably lower K, Na, Si; higher Al, Fe, Ti, Ca), REE and other relatively immobile minor elements are similar to historic and prehistoric Mauna Loa lavas, and the present major-element differences are mainly due to incipient weathering in the tropical environment. New K-Ar whole-rock ages, from relatively fresh roadcut samples, suggest that the age of the Ninole Basalt is approximately 0.1–0.2 Ma, although resolution is poor because of low contents of K and radiogenic Ar. Originally considered the remnants of a separate volcano, the Ninole Hills are here interpreted as faulted remnants of the old south flank of Mauna Loa. Deep canyons in the Ninole Hills, eroded after massive landslide failure of flanks of the southwest rift zone, have been preserved from burial by younger lava due to westward migration of the rift zone. Landslide-induced depressurization of the southwest rift zone may also have induced phreatomagmatic eruptions that could have deposited widespread Basaltic ash that overlies the Ninole Basalt. Subaerial presence of the Ninole Basalt documents that the southern part of Hawaii Island had grown to much of its present size above sea level by 0.1–0.2 Ma, and places significant limits on subsequent enlargement of the south flank of Mauna Loa.     

Geothermometry of Kilauea Iki lava lake,Hawaii

Data on the variation of temperature with time and in space are essential to a complete understanding of the crystallization history of basaltic magma in Kilauea Iki lava lake. Methods used to determine temperatures in the lake have included direct, downhole thermocouple measurements and Fe-Ti oxide geothermometry. In addition, the temperature variations of MgO and CaO contents of glasses, as determined in melting experiments on appropriate Kilauean samples, have been calibrated for use as purely empirical geothermometers and are directly applicable to interstitial glasses in olivine-bearing core from Kilauea Iki. The uncertainty in inferred quenching temperatures is ±8–10° C. Comparison of the three methods shows that (1) oxide and glass geothermometry give results that are consistent with each other and consistent with the petrography and relative position of samples, (2) downhole thermo-couple measurements are low in all but the earliest, shallowest holes because the deeper holes never completely recover to predrilling temperatures, (3) glass geothermometry provides the greatest detail on temperature profiles in the partially molten zone, much of which is otherwise inaccessible, and (4) all three methods are necessary to construct a complete temperature profile for any given drill hole. Application of glass-based geothermometry to partially molten drill core recovered in 1975–1981 reveals in great detail the variation of temperature, in both time and space, within the partially molten zone of Kilauea Iki lava lake. The geothermometers developed here are also potentially applicable to glassy samples from other Kilauea lava lakes and to rapidly quenched lava samples from eruptions of Kilauea and Mauna Loa.     

Isotopic geochemistry of Hualalai shield-stage tholeiitic basalts from submarine North Kona region,Hawaii

The geochemical data of Hualalai tholeiitic basalts allow extension of the temporal variations established at Mauna Loa back in time, and provide important information for the long-term temporal variation of the Hawaiian lavas. We report new Hf, Pb, Nd, and Sr isotope compositions for 32 Hualalai tholeiitic basalts collected from deep submarine portions of the North Kona region. The samples were collected from the lower section of the North Kona bench (dives K218 and K219), a submarine stratigraphic section at Hualalai volcano's northwest rift zone (dive S690), and an elongate ridge outboard of the central section of the bench (dive S692), during two JAMSTEC Hawaii cruises in 2001 and 2002. The Hualalai shield-stage tholeiitic basalts have magma source isotopic signatures similar to Mauna Loa. The new data shows temporal Pb and Sr isotope trends that correspond to the long-term temporal variations in Loa-trend lavas, and the Hualalai–Mauna Loa lavas seem to show inter-shield geochemical excursions. Variation in Pb and Sr isotopes at Hualalai appears to take place over a longer time scale than at Mauna Loa. The merged Hualalai–Mauna Loa isotopic trends support models where heterogeneous material in the plume conduit is distributed chaotically, with variable cross-sectional density and length scale.     

Evidence for contamination of recent Hawaiian lavas from230Th-238U data

²³⁰Th-²³⁸U radioactive disequilibrium was studied in the historical lava flows of the Mauna Loa and Kilauea, Hawaii. Large variations of the (²³⁰Th/²³²Th) ratio among lavas of the same volcano that were erupted at a few years' interval are interpreted as due to contamination. The contamination probably occurs by assimilation of zeolitic minerals formed by seawater interaction while the magma resides in a superficial chamber.     

Helium isotopes and mantle volatiles in Loihi Seamount and Hawaiian Island basalts and xenoliths

We examine in this paper the use of helium isotope ratios for the study of hotspot volcanism along age-progressive island volcanic chains. The Hawaiian Islands are the original “high ³He” hotspot, with ³He/⁴He ratios as high as 32 × the atmospheric ratio; in the Pacific they stand out against the surrounding sea of MORB (rather uniformly 8 × atmospheric) which fills the entire Pacific with the exception of the Macdonald-Mehetia-Samoa axis in the South Pacific. The recent availability of a variety of alkalic and tholeiitic glasses from the U.S. Geological Survey and our own dredge hauls has prompted us to look first at isotopic variability within a single fresh and new volcano which is probably sitting directly atop a mantle plume. Thus we have looked in some detail at the total helium in glass pillow rims, at He in the enclosed vesicles, and at He in the glass itself, in both tholeiitic and alkalic lavas, and also at helium in associated phenocrysts and xenoliths. The measured ³He/⁴He ratios range from atmospheric to 30 × atmospheric, but we see clear evidence that the highly vesiculated lavas suffer exchange of He between the thin glass walls of vesicles and ambient seawater, so that we observe a post-eruptive isotopic disequilibrium between glass and gas phases. The primary effect is the very large loss of initial He content during eruptive vesiculation, which results in quite large isotopic effects from small additions of ambient He (of the order of 0.02 μcc He per gram of basalt; corresponding to a “water/rock ratio” of 0.5). Phenocrystic He in olivines verifies that the gas-phase He is not affected by vesicularities up to about 5%. Alkali basalt He appears to be independent of vesicularity up to values as high as 35%; this He is somewhat lower in ³He/⁴He ratio, but matches precisely the associated xenolithic He. However, from the present data we cannot exclude the possibility that diffusive exchange with seawater has affected the He ratio in alkalic vesicles.On the large scale, along the 10% of the Hawaiian chain available for subaerial sampling, we find high ³He/⁴He ratios (24 × atmospheric) in 5.5 × 10⁶-year-old lavas on Kauai. Maximum values of the ratio so far observed are in the pre-erosional Kula basalts on Maui, confirming the previous results of Kaneoka and Takaoka. Hawaii, where these high values were first observed is now seen to range from MORB ratios at Mauna Loa to only 15 × R_A at Kilauea fumaroles. Most xenolithic He so far measured is MORB He, but Loihi xenoliths have high values and are quite different in this respect. Finally, we discuss also the hydrogen and carbon isotope results on Loihi lavas, and show that these elements resemble MORB and appear not to show a distinctive plume signature.     

Role of olivine cumulates in destabilizing the flanks of Hawaiian volcanoes

The south flank of Kilauea Volcano is unstable and has the structure of a huge landslide; it is one of at least 17 enormous catastrophic landslides shed from the Hawaiian Islands. Mechanisms previously proposed for movement of the south flank invoke slip of the volcanic pile over seafloor sediments. Slip on a low friction décollement alone cannot explain why the thickest and widest sector of the flank moves more rapidly than the rest, or why this section contains a 300 km³ aseismic volume above the seismically defined décollement. It is proposed that this aseismic volume, adjacent to the caldera in the direction of flank slip, consists of olivine cumulates that creep outward, pushing the south flank seawards. Average primary Kilauea tholeiitic magma contains about 16.5 wt.% MgO compared with an average 10 wt.% MgO for erupted subaerial and submarine basalts. This difference requires fractionation of 17 wt.% (14 vol.%) olivine phenocrysts that accumulate near the base of the magma reservoir where they form cumulates. Submarine-erupted Kilauea lavas contain abundant deformed olivine xenocrysts derived from these cumulates. Deformed dunite formed during the tholeiitic shield stage is also erupted as xenoliths in subsequent alkalic lavas. The deformation structures in olivine xenocrysts suggest that the cumulus olivine was densely packed, probably with as little as 5–10 vol.% intercumulus liquid, before entrainment of the xenocrysts. The olivine cumulates were at magmatic temperatures (>1100°C) when the xenocrysts were entrained. Olivine at 1100°C has a rheology similar to ice, and the olivine cumulates should flow down and away from the summit of the volcano. Flow of the olivine cumulates places constant pressure on the unbuttressed seaward flank, leading to an extensional region that localizes deep intrusions behind the flank; these intrusions add to the seaward push. This mechanism ties the source of gravitational instability to the caldera complex and deep rift systems and, therefore, limits catastrophic sector failure of Hawaiian volcanoes to their active growth phase, when the core of olivine cumulates is still hot enough to flow.     

Magma plumbing system of the 2000 eruption of Miyakejima Volcano, Japan

During the 2000 eruption at Miyakejima Volcano, two magmas with different compositions erupted successively from different craters. Magma erupted as spatter from the submarine craters on 27 June is aphyric basaltic andesite (<5 vol% phenocrysts, 51.4–52.2 wt% SiO₂), whereas magma issued as volcanic bombs from the summit caldera on 18 August is plagioclase-phyric basalt (20 vol% phenocrysts, 50.8–51.3 wt% SiO₂). The submarine spatter contains two types of crystal-clots, A-type and A-type (andesitic type). The phenocryst assemblages (plagioclase, pyroxenes and magnetite) and compositions of clinopyroxene in these clots are nearly the same, but only A-type clots contain Ca-poor plagioclase (An < 70). We consider that the A-type clots could have crystallized from a more differentiated andesitic magma than the A-type clots, because FeO*/MgO is not strongly influenced during shallow andesitic differentiation. The summit bombs contain only B-type (basaltic type) crystal-clots of Ca-rich plagioclase, olivine and clinopyroxene. The A-type and B-type clots have often coexisted in Miyakejima lavas of the period 1469–1983, suggesting that the magma storage system consists of independent batches of andesitic and basaltic magmas. According to the temporal variations of mineral compositions in crystal-clots, the andesitic magma became less evolved, and the basaltic magma more evolved, over the past 500 years. We conclude that gradually differentiating basaltic magma has been repeatedly injected into the shallower andesitic magma over this period, causing the andesitic magma to become less evolved with time. The mineral chemistries in crystal-clots of the submarine spatter and 18 August summit bombs of the 2000 eruption fall on the evolution trends of the A-type and B-type clots respectively, suggesting that the shallow andesitic and deeper basaltic magmas existing since 1469 had successively erupted from different craters. The 2000 summit collapse occurred due to drainage of the andesitic magma from the shallower chamber; as the collapse occurred, it may have caused disruption of crustal cumulates which then contaminated the ascending, deeper basalt. Thus, porphyritic basaltic magma could erupt alone without mixing with the andesitic magma from the summit caldera. The historical magma plumbing system of Miyakejima was probably destroyed during the 2000 eruption, and a new one may now form.Editorial responsibility: S Nakada, T Druitt