Geology topics

Michael C. Rowe

Publications and source records attributed to Michael C. Rowe.

7 recordsLinked to original sources

USGS2015

Primative components, crustal assimilation, and magmatic degassing of the 2008 Kilauea summit eruption

Simultaneous summit and rift zone eruptions at Kīlauea starting in 2008 reflect a shallow eruptive plumbing system inundated by a bourgeoning supply of new magma from depth. Olivine-hosted melt inclusions, host glass, and bulk lava compositions of magma erupted at both the summit and east rift zone demonstrate chemical continuity at both ends of a well-worn summit-to-rift pipeline. Analysis of glass within dense-cored lapilli erupted from the summit in March – August 2008 show these are not samplings of compositionally distinct magmas stored in the shallow summit magma reservoir, but instead result from remelting and assimilation of fragments from conduit wall and vent blocks. Summit pyroclasts show the predominant and most primitive component erupted to be a homogenous, relatively trace-element-depleted melt that is a compositionally indistinguishable from east rift lava. Based on a “top-down” model for the geochemical variation in east rift zone lava over the past 30 years, we suggest that the apparent absence of a 1982 enriched component in melt inclusions, as well as the proposed summit-rift zone connectivity based on sulfur and mineral chemistry, indicate that the last of the pre-1983 magma has been flushed out of the summit reservoir during the surge of mantle-derived magma from 2003-2007.

Hawaii↗

USGS2008

Catalog of Mount St. Helens 2004-2007 dome samples with major- and trace-element chemistry

Sampling and analysis of eruptive products at Mount St. Helens is an integral part of volcano monitoring efforts conducted by the U.S. Geological Survey?s Cascades Volcano Observatory (CVO). The objective of our eruption sampling program is to enable petrological assessments of pre-eruptive magmatic conditions, critical for ascertaining mechanisms for eruption triggering and forecasting potential changes in eruption behavior. This report provides a catalog of near-vent lithic debris and new dome-lava collected during 34 intra-crater sampling forays throughout the October 2004 to October 2007 (2004-7) eruptive interval at Mount St. Helens. In addition, we present comprehensive bulk-rock geochemistry for a time-series of representative (2004-7) eruption products. This data, along with that in a companion report on Mount St. Helens 2004 to 2006 tephra by Rowe and others (2008), are presented in support of the contents of the U.S. Geological Survey Professional Paper 1750 (Sherrod and others, eds., 2008). Readers are referred to appropriate chapters in USGS Professional Paper 1750 for detailed narratives of eruptive activity during this time period and for interpretations of sample characteristics and geochemical data. The suite of rock samples related to the 2004-7 eruption of Mount St. Helens and presented in this catalog are archived at the David A. Johnson Cascades Volcano Observatory, Vancouver, Wash. The Mount St. Helens 2004-7 Dome Sample Catalogue with major- and trace-element geochemistry is tabulated in 3 worksheets of the accompanying Microsoft Excel file, of2008-1130.xls. Table 1 provides location and sampling information. Table 2 presents sample descriptions. In table 3, bulk-rock major and trace-element geochemistry is listed for 44 eruption-related samples with intra-laboratory replicate analyses of 19 dacite lava samples. A brief overview of the collection methods and lithology of dome samples is given below as an aid to deciphering the dome sample catalog. This is followed by an explanation of the categories of sample information (column headers) in Tables 1 and 2. A summary of the analytical methods used to obtain the geochemical data in this report introduces the presentation of major- and trace-element geochemistry of 2004-7 Mount St. Helens dome samples in table 3. Intra-laboratory results for the USGS AGV-2 standard are presented (tables 4 and 5), which demonstrate the compatibility of chemical data from different sources.

Open-File Report↗

USGS2008

Catalog of Mount St. Helens 2004 - 2005 tephra samples with major- and trace-element geochemistry

This open-file report presents a catalog of information about 135 ash samples along with geochemical analyses of bulk ash, glass and individual mineral grains from tephra deposited as a result of volcanic activity at Mount St. Helens, Washington, from October 1, 2004 until August 15, 2005. This data, in conjunction with that in a companion report on 2004-2007 Mount St. Helens dome samples by Thornber and others (2008a) are presented in support of the contents of the U.S. Geological Survey Professional Paper 1750 (Sherrod and others, ed., 2008). Readers are referred to appropriate chapters in USGS Professional Paper 1750 for detailed narratives of eruptive activity during this time period and for interpretations of sample characteristics and geochemical data presented here. All ash samples reported herein are currently archived at the David A. Johnston Cascades Volcano Observatory in Vancouver, Washington. The Mount St. Helens 2004?2005 Tephra Sample Catalogue along with bulk, glass and mineral geochemistry are tabulated in 6 worksheets of the accompanying Microsoft Excel file, of2008-1131.xls. Samples in all tables are organized by collection date. Table 1 is a detailed catalog of sample information for tephra deposited downwind of Mount St. Helens between October 1, 2004 and August 18, 2005. Table 2 provides major- and trace-element analyses of 8 bulk tephra samples collected throughout that interval. Major-element compositions of 82 groundmass glass fragments, 420 feldspar grains, and 213 mafic (clinopyroxene, amphibole, hypersthene, and olivine) mineral grains from 12 ash samples collected between October 1, 2004 and March 8, 2005 are presented in tables 3 through 5. In addition, trace-element abundances of 198 feldspars from 11 ash samples (same samples as major-element analyses) are provided in table 6. Additional mineral and bulk ash analyses from 2004 and 2005 ash samples are published in chapters 30 (oxide thermometry; Pallister and others, 2008), 32 (amphibole major elements; Thornber and others, 2008b) and 37 (210Pb; 210Pb/226Pa; Reagan and others, 2008) of U.S. Geological Survey Professional Paper 1750 (Sherrod and others, 2008). A brief overview of sample collection methods is given below as an aid to deciphering the tephra sample catalog. This is followed by an explanation of the categories of sample information (column headers) in table 1. A summary of the analytical methods used to obtain the geochemical data in this report introduces the presentation of major- and trace-element geochemistry of Mount St. Helens 2004-2005 tephra samples in tables 2-6. Rhyolite glass standard analyses are reported (Appendix 1) to demonstrate the accuracy and precision of similar glass analyses presented herein.

Washington↗

USGS2008

Identification and evolution of the juvenile component in 2004-2005 Mount St. Helens ash

Petrologic studies of volcanic ash are commonly used to identify juvenile volcanic material and observe changes in the composition and style of volcanic eruptions. During the 2004-5 eruption of Mount St. Helens, recognition of the juvenile component in ash produced by early phreatic explosions was complicated by the presence of a substantial proportion of 1980-86 lava-dome fragments and glassy tephra, in addition to older volcanic fragments possibly derived from crater debris. In this report, we correlate groundmass textures and compositions of glass, mafic phases, and feldspar from 2004-5 ash in an attempt to identify juvenile material in early phreatic explosions and to distinguish among the various processes that generate and distribute ash. We conclude that clean glass in the ash is derived mostly from nonjuvenile sources and is not particularly useful for identifying the proportion of juvenile material in ash samples. High Li contents (>30 μg/g) in feldspars provide a useful tracer for juvenile material and suggest an increase in the proportion of the juvenile component between October 1 and October 4, 2004, before the emergence of hot dacite on the surface of the crater on October 11, 2004. The presence of Li-rich feldspar out of equilibrium (based on Liplagioclase/melt partitioning) with groundmass and bulk dacite early in the eruption also suggests vapor enrichment in the initially erupted dacite. If an excess vapor phase was, indeed, present, it may have provided a catalyst to initiate the eruption. Textural and compositional comparisons between dome fault gouge and the ash produced by rockfalls, rock avalanches, and vent explosions indicate that the fault gouge is a likely source of ash particles for both types of events. Comparison of the ash from vent explosions and rockfalls suggests that the fault gouge and new dome were initially heterogeneous, containing a mixture of conduit and crater debris and juvenile material, but became increasingly homogeneous, dominated by juvenile material, by early January 2005.

Washington↗

USGS2008

Chemistry, mineralogy, and petrology of amphibole in Mount St. Helens 2004-2006 dacite

Textural, compositional, and mineralogical data are reported and interpreted for a large population of clinoamphibole phenocrysts in 22 samples from the seven successive dacite spines erupted at Mount St. Helens between October 2004 and January 2006. Despite the uniformity in bulk composition of magma erupted since 2004, there is striking textural and compositional diversity among amphibole phenocrysts and crystal fragments that have grown from, partly dissolved in, or been accidentally incorporated in the new dacite. This study demonstrates that magma erupted throughout the current dome-building episode is the end product of small-scale, thorough mixing of multiple generations of crystal-laden magma. The mixed amphibole population provides important clues to magma conditions within the dacite magma reservoir prior to ascent and, to some extent, the dynamics of mixing and ascent. The predominant amphibole in new dome rock ranges from moderate- to high-alumina tschermakite and magnesiohastingsite compositions. As substantiated by major- and trace-element geochemistry and barometry calculations, this compositional range of crystals, along with plagioclase, orthopyroxene, and iron-titanium oxide, is likely to have precipitated from dacite magma over a range of pressures and temperatures consistent with experimentally determined phase relations (~900°C to ~800°C between 100 MPa and ~350-400 MPa or ~4-km and 13.5-15-km depth). Along with traceelement characteristics, textural and compositional data help to distinguish some low-alumina magnesiohornblende crystals as xenocrysts. The diverse range in composition of amphibole in all samples of 2004-6 dacite, and the complex zonation observed in many phenocrysts, suggests a well-mixed source magma with components that are subjected to repeated heating and (or) pressurization within this pressure-temperature window. Amphibole textural and compositional diversity suggest dynamic conditions in the upper-reservoir zone, which has been tapped steadily during ~2 years of continuous and monotonous eruption. This well-mixed crystal mush is likely to have been subjected to repeated injection of hotter magma into cooler crystal-laden magma while simultaneously assimilating earlier generations of dacitic roof material and surrounding gabbroic rock. Decompression-related reaction rims around subhedral, rounded, resorbed, and fragmented amphibole phenocrysts, regardless of composition, indicate that this mixed-crystal assemblage was being broken, abraded, and dissolved in the magma as a result of mechanical mixing before and during early stages of ascent from conduit roots extending into a mushy cupola of the shallow reservoir. In the earliest lava samples (October 2004), amphiboles with <3-μm rims associated with a glassier matrix than later samples suggest a slightly faster ascent rate consistent with the relatively high eruptive flux of the earliest phases of dome extrusion. Reaction rim widths of ~5 μm on amphibole in all subsequently extruded lava result from a steady influx and upward transport of magma from 3.5-2.5-km to ~1-km depth at rates of ~600 to ~1,200 m/day, through a conduit less than 10 m in radius. Slower ascent rates inferred from volumetric-flux and matrixcrystallization parameters are explained by a widening of the conduit to greater than 60 m radius within 1 km of the surface.

Washington↗

USGS2008

Trace element and Pb isotope composition of plagioclase from dome samples from the 2004-2005 eruption of Mount St. Helens, Washington

We report the results of in-situ laser ablation ICP–MS analyses of anorthite content, trace-element (Li, Ti, Sr, Ba, La, Pr, Ce, Nd, Eu, Pb) concentrations, and Pb-isotope compositions in plagioclase from eight dome-dacite samples collected from the 2004-5 eruption of Mount St. Helens and, for comparison, from three dome samples from 1981-85. For 2004-5 samples, plagioclase phenocrysts range in composition from An 30 to An 80 , with the majority An 42 -An 65 . With the exception of Li, the range of trace-element abundances in plagioclase phenocrysts is largely constant in material erupted between October 2004 and April 2005 and is broadly consistent with the 1983-85 dome samples. Anomalously high Li contents in the early stage of the eruption are thought to reflect addition of Li to the upper part of the magma chamber immediately before eruption (within ~1 year) by transfer of an alkali-enriched, exsolved vapor from deep within the magma chamber. Other trace elements show significant correlations (at >99 percent confidence limits) with anorthite content in plagioclase phenocrysts--Ba, light rareearth elements (LREE), and Pb show positive correlations, whereas Ti and Sr correlate negatively. Variations in plagioclase-melt partitioning as a function of anorthite content cannot explain trace-element variations--in particular predicting trends for Ti and Sr opposite to those observed. A simple model involving closed-system fractional crystallization of plagioclase + hypersthene + amphibole + oxides largely reproduces the observed trends. The model requires no gain or loss of plagioclase and is consistent with the lack of europium anomalies in bulk dacite samples. Analytical traverses within individual plagioclase phenocrysts support this model but also point to a diversity of melt compositions present within the magma storage zone in which plagioclase crystallized. Plagioclase crystals from gabbronorite inclusions in three dacite samples have markedly different trace-element and Pbisotope compositions from those of plagioclase phenocrysts, despite having a similar range of anorthite contents. Inclusions show some systematic differences from each other but typically have higher Ti, Ba, LREE, and Pb and lower Sr and have lower 208 Pb/ 206 Pb and 207 Pb/ 206 Pb ratios than coexisting plagioclase phenocrysts. The compositions of plagioclase from inclusions cannot be related to phenocryst compositions by any reasonable petrologic model. From this we suggest that they are unlikely to represent magmatic cumulates or restite inclusions but instead are samples of mafic Tertiary basement from beneath the volcano.

Washington↗

USGS2007

Mount St. Helens Petrology Workshop

Following seismic activity in late September 2004, the current eruption of Mount St. Helens began with an explosive steam and ash emission on 1 October 2004, with hot dacite emerging from the crater floor on 11 October 2004. Nearly two years later, with more than 80 million cubic meters of erupted dacite, accompanied by rare explosions and predominantly shallow seismicity questions still remain about what initiated and what is sustaining the eruption. The U.S. Geological Survey's (USGS) Cascade Volcano Observatory (CVO) hosted the 2006 Mount St. Helens Petrology Workshop in Vancouver, Wash., on 27–30 August 2006. With many of the more than 40 workshop participants finalizing contributions to a USGS Professional Paper on the current Mount St. Helens eruption, the workshop was a timely opportunity to share results, reconcile interpretations, and plan future research.

Washington↗