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Thomas L. Wright

Publications and source records attributed to Thomas L. Wright.

34 records · Page 2Linked to original sources
USGS1986

Volcano monitoring at the U.S. Geological Survey's Hawaiian Volcano Observatory

The island of Hawaii has one of the youngest landscapes on Earth, formed by frequent addition of new lava to its surface. Because Hawaiian are generally nonexplosive and easily accessible, the island has long attracted geologists interested in studying the extraordinary power of volcanic eruptions. The U.S. Geological Survey's Hawaiian Volcano Observatory (HVO), now nearing its 75th anniversary. has been in the forefront of volcanology since the 1900's. This issue of Earthquakes and volcanoes is devoted to the work of the Observatory and its role in studying the most recent eruptions of Hawaii's two currently active volcanoes, Kilauea and Mauna Loa.

Hawaii↗
USGS1978

A computer-assisted graphical method for identification and correlation of igneous rock chemistries

We have devised a computer-assisted graphical method for correlating chemical analyses in suites of related igneous rocks. The method provides a direct and empirical means of sample identification using all of the reported chemistry. In a study of basalt of the Columbia River plateau, the method has been used for (1) checking field identifications of rocks, (2) spotting analytical errors in analyses of samples of known chemical type, (3) identifying repetitions of chemistry in thick stratigraphic sections, and (4) matching analyses of dikes to those of flows that the dikes may have fed. Program OXVAR creates a set of oxide-oxide variation diagrams on a CALCOMP plotter; any oxide may be used as the base (for example, MgO, SiO 2 ). For each oxide-oxide variation diagram, program CTSET creates the smallest convex polygon that encloses all the data points as well as a larger polygon that takes into account the error in determination of each data point. A set of nested polygons, one for each oxide, then represents a chemical type. Program CTYPE identifies unknown analyses by comparing them with all defined chemical types. If all the elements or oxides of an analysis plot within the defined polygons for a given chemical type, then an identification is printed. If at least one element of an analysis falls outside the set of polygons defined for each chemical type, then “unidentified” is printed, and qualitative information on the amount of deviation from the defined chemical types is given.

Geology↗
USGS1975

Chemical compositions of Kilauea east-rift lava, 1968–1971

The major element chemical compositions of lava from four eruptions on the east rift zone of Kilauea between August 1968 and October 1971 reflect three petrologic processes: Production of chemically distinct batches of magma in the mantle. Separation of olivine, augite, and plagioclase from liquid during flow in the rift-zone conduits. Mixing of different magmas during ascent to the surface. Chemically none of the four Kilauea east-rift eruptions matches the preceding summit eruption in Halemaumau that ended in July 1968. The Mauna Ulu eruption, May 1969 to October 1971 (the last of flie east-rift eruptions), can be divided into five olivine-controlled and chemically distinct variants. Three of these characterize the first seven months of the eruption and are closest in composition to the 1967–8 Halemaumau eruption. Variants 4 and 5 were erupted later and have compositions that are distinctly different from that of the 1967–8 eruption. Major differences are higher Al 2 O 3 (0·15–0·23 per cent), and lower K 2 O (0·07–0·10 per cent) and TiO 2 (0·12–0·23 per cent) in variants 4 and 5 at the same MgO content. Some lavas from eruptions in August and October 1968 and February 1969, have olivine-controlled magma compositions that are identical to mixtures of Mauna Ulu variants 1–3 and the 1967–8 composition. This observation fits an hypothesis advanced earlier by T. L. Wright and R. S. Fiske that magmas in the central magma chamber become mixed with magmas in the rift zone and can be identified as mixing components of rift eruption magmas before they appear as distinctive magmas in summit eruptions. Lavas representing mixing of olivine-controlled magma with differentiated magma were erupted in October 1968, February 1969, and in May and December 1969. The changes in amount of K 2 O and TiO 2 during the latter part of the 1969–71 Mauna Ulu eruption are the reverse of the overall secular change in composition of Kilauea summit lavas from pre-1750 through 1967–8. The K 2 O and TiO 2 contents of the latest overflows during the 1969–71 Mauna Ulu eruption (April 1971) are comparable to that of lava erupted at Kilauea summit prior to 1750. The changing chemistry of Kilauea magma is found to be of use as a ‘tracer’ in the complex Kilauea conduit system. Application of these data to older lava sequences is difficul because of the complexity of the processes controlling lava composition and the absence of detailed information about the time-space chemical variation during individual eruptions.

Hawaii↗
USGS1973

Chemical variation related to the stratigraphy of the Columbia River basalt

Study of major element chemical analyses of Columbia River basalt leads to a grouping of most of the analyses into 11 chemical types which are distinguished with little overlap on a SiO 2 -MgO variation diagram. Other diagnostic variation diagrams are total iron (‘FeO’)-MgO, K 2 O-MgO, and TiO 2 -MgO. A four-unit informal stratigraphy has been adopted in order to define the relations between chemical composition and stratigraphic position. From oldest to youngest, the four stratigraphic units are (1) lower basalt of Bond (1963) and Picture Gorge basalt, (2) lower Yakima basalt, (3) middle Yakima basalt, and (4) upper Yakima basalt. Most of the Picture Gorge and lower basalt flows are relatively rich in MgO (approximately 4.5 to 7.1 percent) and are distinguished by intermediate SiO 2 relative to MgO. Furthermore, the Picture Gorge basalt generally has low K 2 O relative to MgO. The lower Yakima basalt consists almost entirely of flows with relatively low MgO content (approximately 3.0 to 5.5 percent) and with the highest SiO 2 relative to MgO of any flows of the Columbia River basalt. The middle Yakima basalt contains flows of three distinct chemical types, which together cover the same MgO range as the lower Yakima flows but which have considerably lower SiO 2 and higher ‘FeO’ and TiO 2 relative to MgO. Flows in the upper Yakima basalt are of diverse composition; two of the youngest flows are distinguished by having the lowest SiO 2 and highest ‘FeO’, TiO 2 , and P 2 O 5 relative to MgO of any analyzed Columbia River basalt. Flows of one or more chemical types may form the dominant lithology in a stratigraphic unit, but single flows of the same chemical types may occur in any stratigraphic unit. Some lava sampled in the eastern part of the plateau has more TiO 2 than does lava of otherwise similar composition sampled in the western part of the plateau. This is tentatively interpreted as reflecting a heterogeneous composition for the mantle beneath the Columbia Plateau.

Oregon, Washington↗
USGS1973

Magma Mixing as Illustrated by the 1959 Eruption, Kilauea Volcano, Hawaii

The 1959 eruption of Kilauea volcano is unique among recent Kilauea summit eruptions (1952 to 1968) in at least two respects: (1) a large collapse of Kilauea summit accompanied the eruption, and (2) the erupted lavas show a complex variation in their bulk chemical composition. Both features suggest that the 1959 eruption was fed from a source different from that which fed other summit eruptions in this period. The variations in chemical composition can be interpreted in terms of mixing chromite-bearing olivine with variable proportions of two “end-member” magmas represented by the composition of samples of pumice erupted during the first phase of the eruption. Mixing calculations show that the MgO content of olivine varies with the MgO content of the lava and thus with olivine percentage in the same manner as previously determined by Richter and Murata (1966) from petrographic study of hand samples. The calculations also show that the proportion of the two end-member magma types varies throughout the eruption. These results suggest that the eruption was fed from two separate magma batches, each of which was held in a reservoir with an olivine-poor top and olivine accumulation toward the bottom. There is also evidence that the two end-member magmas may be related by redistribution of clinopyroxene in a third hypothetical magma. The complex pre-eruption history implied by the chemical data is at present not satisfactorily explained by any physical model of fractionation, storage, and mixing that can be inferred from data on other well-studied Kilauea eruptions. The average MgO content (15.5 percent) of the 1959 eruption is estimated to be in minimum MgO content of magma produced by partial melting in the mantle beneath Kilauea.

Hawaii↗
USGS1972

Apollo 11 and 12 mare basalts and gabbros: Classification, compositional variations, and possible petrogenetic relations

On the basis of composition, it is possible to distinguish three major groups of Apollo 12 basaltic rocks: olivine-pigeonite basalts and gabbros, ilmenite-bearing basalts and gabbros, and feldspathic basalts. Two major groups of Apollo 11 basalts are also distinguishable: ophitic ilmenite basalts and intersertal ilmenite basalts. Compositional variations between samples within groups are generally dominated by MgO variations, whereas differences between groups are primarily inverse variations of TiO 2 and SiO 2 or Al 2 O 3 and FeO. Results of fractionation calculations indicate that the MgO variation trends are explained principally by low-pressure fractionation of early-crystallized olivine ± pigeonite ± chrome spinel. The Al 2 O 3 versus FeO trend in the basalts might possibly be explained by near-surface fractionation, but the TiO 2 versus SiO 2 trend is not explainable in this way. Investigations of the latter trend in terms of possible processes of high-pressure fractional melting or fractional crystallization indicate that the compositional variations cannot be the products of simple variations in depth or degree of fractionation. Our data are consistent with the view that the mafic magmas formed by partial melting in the lunar interior, and that near-surface fractionation, with the exception of removal or addition of olivine, has not been extensive.

GSA Bulletin↗
USGS1971

Origin of the differentiated and hybrid lavas of Kilauea Volcano, Hawaii

Kilauea Volcano has erupted lava from its summit caldera and from two rift zones that extend from the summit towards the east and south-west. Lavas erupted from the summit of the volcano differ from each other principally in their content of olivine and define lines of ‘olivine control’ on magnesia variation diagrams. Lavas erupted on the rift zones may be similar in composition to the summit lavas or may be differentiated by processes that involve minerals other than olivine. All of the differentiated lavas have less than 6·8 per cent MgO and plot off the extension of olivine control lines for the summit lavas. Prehistoric vents (before A.D. 1750) from which differentiated lavas have been erupted are found on the east rift zone and in the western Koae fault zone adjacent to the south-west rift zone; historic vents for differentiated lavas are confined to the east rift zone. Twenty-one new analyses are presented for several of the east rift differentiates and for the newly discovered differentiates adjacent to the south-west rift zone. The differentiates have MgO as low as 3·9 per cent and SiO 2 as high as 56 per cent; both extremes are found in the prehistoric lavas adjacent to the south-west rift. Detailed petrochemical studies suggest the following conclusions: The chemical composition of magma erupted at Kilauea summit varies with the date of eruption. Lavas erupted before 1750, during the eighteenth and nineteenth centuries, and in the twentieth century form groups that can be distinguished chemically. On a lesser scale, each Kilauea summit eruption in the twentieth century has a chemistry that is distinctive with respect to the chemistry of every other summit eruption. During late prehistoric time pockets of differentiated magma were formed within the rift zones by separation of the liquid remaining after partial crystallization of bodies of summit magma. This process presumably is still going on within the east rift zone, but the more recently separated liquids have not yet been erupted to the surface. The relative time at which these differentiated magmas were produced can be estimated from calculations based on their chemical compositions, which show that the differentiates could lie on the liquid line of descent for Kilauea summit magma of prehistoric composition but not on any liquid line of descent for younger summit magmas. Lava from some eruptions, notably the early part of the 1955 eruption on the lower east rift, has the composition of the liquid fraction as it is generated within the rift. Lava compositions of other eruptions, including those of the later lavas of 1955, are best explained by mixing of magma supplied from a central reservoir beneath Kilauea summit with the differentiated liquid in the rift. Lava from each summit eruption is unique chemically, so it is possible to recognize its presence or absence as components of mixing in such mixed lavas. It appears that summit magma of composition characteristic of the 1952 and 1961 Halemaumau eruptions contributed to the composition of the mixed lavas produced in the latter part of the 1955 eruption. Summit magma of 1961 composition is alone sufficient to explain the composition of mixed lavas erupted in 1960 and 1961. In rift lavas erupted from 1962 to 1965, the composition of lava erupted in Halemaumau in 1967, in addition to the 1961 composition, is a component of mixing, and it is the dominant summit component in the composition of the two 1965 eruptions. The proportion of summit magma to differentiated magma needed to explain the composition of lavas erupted on the upper east rift increases from 1961 to 1965; this increase indicates that the differentiated magma was being diluted and used up by repeated flooding of this part of the rift zone by magma supplied from the central reservoir. The fact that components of ‘summit composition’ appear in rift eruptions before they appear undiluted in Halemaumau suggests that the central reservoir is vertically zoned. Rift eruptions are fed from lower levels where younger magma is available, and summit eruptions are fed from the relatively older magma above. The chemical distinction between lava of successive summit eruptions implies that significant convective mixing of magma does not take place throughout the central reservoir. The unique and uniform composition of lava of each successive summit eruption also suggests that summit eruptions end when all of the magma of one composition has been erupted. The magma erupted from the upper levels of the reservoir during one cycle is continually replaced from below by younger magma of different composition. In order for eruption to be renewed in Halemaumau, new magma from the mantle must be held in storage at intermediate levels before it attains an ‘eruptive state’. The hypothesis presented in 2–4 above permits qualitative predictions concerning future lava compositions. The composition of the next lava to be erupted in Halemaumau is expected to be distinct from that of the 1967 eruption, and this composition will presumably be identified in rift eruptions occurring between 1967 and the time of its appearance in Halemaumau. Differentiates of prehistoric age also were apparently formed in the same way as those of historic age, but the mixing cannot be described quantitatively because of poor control on the stratigraphy and the compositions of erupted lavas. One lava in the Koae group, that from Yellow Cone, appears to be a mixture of a picritic magma (12 per cent MgO) with a differentiated liquid with less than 2·5 per cent MgO and nearly 60 per cent SiO 2 .

Hawaii↗
USGS1970

A linear programming and least squares computer method for solving petrologic mixing problems

Problems of petrologic mixing have been solved using a two-stage computer-based calculation. First, linear programming is used to obtain an approximate solution and to identify non-negative solution values. Then a conventional least squares calculation is performed using the analyses represented by non-negative solution values as input to yield an optimum set of solution values. The error attached to each solution value is estimated by an empirical procedure. Petrologic application of the program has been demonstrated with three types of calculations: chemical mode, magma mixing, and liquid line of descent.

GSA Bulletin↗
USGS1969

Kilauea Volcano: The 1967-68 summit eruption

On 5 November 1967 Kilauea volcano began erupting lava from vents on the floor of its summit pit crater. Halemaumau, 170 meters deep. This eruption ended nearly 2 years of the quiescence that followed a short lived eruption on the east rift zone of Kilauea in December 1965 (1). The 1967-68 eruption was the first activity in Halemaumau since July 1961 (2). The eruption ceased on 13 July 1968 following 31 separate phases of fountaining separated by short periods of quiescence. Six weeks after the end of the summit eruption, a short eruption occurred on the upper east rift zone of Kilauea. As the article goes to press there have been four eruptions, all of the upper east rift zone. The last of the four began in May 1969 and have just completed its seventh phase. The article summarizes the eruption in Halemanumau and complements an article Fiske and Kinoshita on the deformation that preceded the eruption (3). The methods of study and the instrumentation used during the eruption are the same as those discussed in the earlier article. The locations of all seismographs tiltmeter stations and bench marks are shown in Fig. 1.

Hawaii↗
USGS1968

Mineralogy of sulfides from certain Hawaiian basalts

Polymineralic sulfide grains, composed principally of Fe sulfide and Fe-Cu sulfide, with magnetite, have been studied mineragraphically and by electron probe, and interpreted in terms of experimental data for the system Fe-Ni-Cu-S. The three main phases are monosulfide solid solution, a Cu-Fe sulfide (solid solution) with composition near cubanite, and Ti-free magnetite. The grains are believed to represent phases unmixed from an immiscible liquid phase in the basalt magma. Compositions of the two main sulfide phases suggest quenching below 700 degrees C. Most of the Ni has been retained in the monosulfide solid solution by rapid quenching.

Hawaii↗