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T. L. Wright

Publications and source records attributed to T. L. Wright.

26 records · Page 2Linked to original sources
USGS1974

Presentation and interpretation of chemical data for igneous rocks

Arguments are made in favor of using variation diagrams to plot analyses of igneous rocks and their derivatives and modeling differentiation processes by least-squares mixing procedures. These methods permit study of magmatic differentiation and related processes in terms of all of the chemical data available. Data are presented as they are reported by the chemist and specific processes may be modeled and either quantitatively described or rejected as inappropriate or too simple. Examples are given of the differing interpretations that can arise when data are plotted on an AEM ternary vs. the same data on a full set of MgO variation diagrams. Mixing procedures are illustrated with reference to basaltic lavas from the Columbia Plateau.

Idaho, Washington, Oregon↗
USGS1966

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 SiO 2 , 2.4 percent Na 2 O, and 0.54 percent K 2 O. 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 Al 2 O 3 ; and higher total iron, TiO 2 , Na 2 O, K 2 O, P 2 O 5 , and F, and, in most samples, SiO 2 . 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.

Hawaii↗
USGS1966

Deformation measurements on Kilauea volcano, Hawaii

Repeated electronic distance measurements across Kilauea Caldera with Tellurometers and Geodimeter show definite horizontal expansion related to the vertical uplift and outward tilting of the summit prior to an eruption, and contraction during and after a flank eruption. Measurements started in October 1964, along a 3098 meter line between Uwekahuna and Keanakakoi, indicate a relatively uniform lengthening of 12 centimeters during the interval October 22, 1964 to March 1, 1965. Rapid shortening of the line by 28 centimeters was measured 4 days after the beginning of a flank eruption which involved emission of approximately 29 million cubic meters of lava during the period March 5 to March 15, 1965. During the expansion, the standard deviation of 10 Tellurometer measurements from a least-squares srtaight line solution is ± 2.0 centimeters (6.5 ppm) whereas 9 Geodimeter measurements have a standard deviation of ± 1.1 (3.6 ppm) centimeters. Absolute distance readings between the two instruments differ by 4 centimeters (13 ppm), but relative changes in distance were the same on both instruments. Changes in distance across Kilauea Caldera can, therefore, be easily measured to accuracies of 4 to 7 parts per million with standard electronic distance measuring systems. On active volcanoes where ground surface deformation exceeds 10–100 parts per million with changes in subsurface magma pressure or volume, repeated horizontal distance measurements can be a most useful technique.

Hawaii↗
USGS1966

Oxygen fugacities directly measured in magmatic gases

An electrochemical device was used to measure the fugacity of oxygen ( f O2 ) in holes drilled through the crust of Makaopuhi lava lake, Kilauea Volcano, Hawaii. Results obtained within 6 months of the lake formation show that log f O2 normally varies linearly with the reciprocal of the absolute temperature, and that chemical changes occurring in the cooling tholeiitic basalt are reflected in the f O2 values measured in the holes.

Hawaii↗
USGSDate not supplied

Xenoliths in the honolulu volcanic series, Hawaii

The Pleistocene to Holocene Honolulu Volcanic Series was erupted from about 37 vents scattered over the older Koolau tholeiite shield. The rocks of this series are compositionally zoned with respect to the shield; near the Koolau caldera the predominant rocks are melilitenepheline basalts, but these give way outward to nepheline basalts, and ultimately, at the apron of the shield, to alkalic olivine basalts. The xenoliths in these are likewise zoned: most of those in the caldera area consist of dunite, most of those at intermediate distances of lherzolite, and some of those in the apron of the shield consist of garnet pyroxenite and peridotite. The zoning of the xenoliths, however, does not coincide with that of the enclosing rocks. We believe that copious eruption of Koolau tholeiite produced a lateral and vertical heterogeneity in the mantle beneath Oahu, and that the zoning in both Honolulu lavas and their xenoliths is caused by that heterogeneity. The textures of the xenoliths indicate that the basalts were mainly produced by fractional melting rather than fractional crystallization. There is some evidence that the dunite xenoliths are mantle residua produced during the generation of the tholeiite, and that the Honolulu magmas were generated at greater depths than the Koolau magmas, probably as a result of elastic unloading. © 1970 Oxford University Press.

Hawaii↗