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Norman G. Banks

Publications and source records attributed to Norman G. Banks.

15 recordsLinked to original sources
USGS1980

Geology of a zone of metamorphic core complexes in southeastern Arizona

An elongate northwest-trending zone of batholith-size metamorphic core complexes extends some 130 km from the Rincon Mountains to the Picacho Mountains in southeastern Arizona. The complexes are characterized by undeformed to gneissic granitic intrusions, gneissic to phyllonitic xenoliths and wall rocks derived mainly from Precambrian granitic rock, shallow-dipping foliation, and remarkably uniform directions of lineation. Parts of this zone have been recognized and studied extensively for more than 30 yr, but there remains a divergence of opinion about the age, depth of emplacement, and origin of the complexes. Field relations indicate that host rocks as young as or younger than Mesozoic were involved in cataclasis. K-Ar and fission-track ages indicate that the complexes were at temperatures uniformly in excess of 400°C in the middle Tertiary (20 to 30 m.y. ago) and that the bedrock between and very near the complexes was not thermally affected. Tertiary plutons characteristically associated with the high-grade metamorphic rocks are also cataclastically deformed, and stratigraphic depths to the top of metamorphic terranes were no more than 6 km and possibly less than 3 km. These and other data suggest to some that the complexes developed during intrusion of composite batholiths at shallow depth in an anisotropic stress field during the middle Tertiary. On the other hand, Rb-Sr and U-Th-Pb techniques yielded older ages (≥44 m.y.) for some samples. These and additional data suggest to others that major development of cataclasis preceded the middle Tertiary and included regional thrusting.

Arizona↗
USGS1980

A catalogue of drill core recovered from Kilauea Iki lava lake, from 1967 to 1979

The purpose of this report is to serve as a descriptive catalogue for drill core recovered from Kilauea Iki lava lake, from 1967 to 1979. Kilauea Iki lava lake was formed when lavas of the 1959 summit eruption were ponded in Kilauea Iki pit crater, a large pit crater at the extreme upper end of Kilauea's east rift zone (Fig. 1). This eruption is one of the best documented of Kilauean eruptions: Murata and Richter (1966) and Richter and Murata (1966) presented data on the chemistry and petrography of the lavas, respectively, and Richter et al. (1970) described the complex filling of the pit crater in considerable detail. Investigation of the lava lake began a few months after the crust stabilized, with the establishment of two perpendicular lines of levelling stations on the surface of the lake. In 1960-62, four holes were drilled through the upper crust in the center of the lake; the crust was 22-44 feet (6.7-13.4 m) thick at that time. Richter and Moore (1966) presented petrographic, modal, and chemical data on the core recovered from this early drilling. The upper crust of Kilauea Iki was drilled again in 1967 by staff members of the Hawaiian Volcano Observatory, and core was recovered from three holes. In 1975, U.S. Geological Survey workers drilled three more holes, each a few feet away from one of the 1 967 holes. A summary of all work done on Kilauea Iki and other Hawaiian lava lakes through 1975 has been given by Wright et al. (1976). The lake has been redrilled twice since 1975, by workers from Sandia Laboratories, as part of their Magma Energy Research program, in cooperation with the U.S. Geological Survey. In 1976, they drilled two holes near the center of the lake. In 1978-79, they drilled a total of six holes; one, commissioned by the U.S. Geological Survey, went completely through the lava lake near its north edge, into the pre-1959 lavas below.

Hawaii↗
USGS1977

Some observations that bear on the origin of porphyry copper deposits

Observations at Ray, Ariz., suggest that upper crustal calc-alkaline plutons associated in time and space with the deposit might not have been capable of producing much water by differentiation and that any water released likely had restricted access to the best copper-sulfur sources in the magmas. Observation of concentrations of sulfides around isolated pockets of partially melted rocks below the Stillwater Complex. Mont., suggest to us a variant model of porphyry copper generation that does not require calc-alkaline plutons to be the vessels that transport copper and sulfur to upper crustal sites.

Open-File Report↗
USGS1977

Magmatic behavior of Cu, S, Cl, F, and H 2 O in igneous rocks associated with the Ray porphyry copper deposit, Arizona

Porphyry copper deposits are the subject of a large volume of literature indicating that controversy still reigns as to which model or combination of models explains their origin, and yet, over 70 years ago we reached agreement that the well-documented space-time relationship between the deposits and calc-alkaline plutons indicates a genetic tie between them. This genetic tie is generally assumed to indicate a causitive role for an exposed or nearby hidden pluton. There are many variants, but the two end-member models that incorporate this causitive assumption are the meteoric water model and the orthomagmatic model. It is my opinion that the controversy originates from use of indirect data and variant models to explain new observational data and experimental studies that threaten the survival of the basic end-member models. One of many examples of this is the end-stage magmatic evolution of chlorine-rich water required of the orthomagmatic model. This evolution is required because the low copper content of calc-alkaline plutons demands a large source magma, that, because it generally is not visible, has to be buried. Additionally, much of the ore minerals in porphyry deposits is along fractures. Both conditions require transportation of the ore components from the magma, and to transport enough ore components, given the limited amount of water soluble in a melt and the low solubility of base-metal sulfides in water without benefit of chloride complexing, we required of the original Lindgren magmatic model that the source pluton produced chloride-rich water. However, we did not investigate the rocks associated with deposits to substantiate the hypothesis. We went to the laboratory and found that sufficient water and chlorine could be dissolved in silicate melt in a gold capsule in a high-pressure high-temperature bomb to allow postulation of sufficient water and chlorine in the stocks associated with porphyry deposits; in other words, we invested in indirect rather than direct studies.

Arizona↗
USGS1977

Middle Tertiary plutonism in the Santa Catalina and Tortolita mountains, Arizona

Recent reconnaissance geologic mapping in the Santa Catalina and Tortolita Mountains of southeastern Arizona, supplemented by new and published potassium-argon and fission-track ages, suggests that a large composite batholith of middle Tertiary (about 25 million years) age crops out extensively in both mountains. More than two-thirds of the batholith and contiguous wallrocks is gneissic, the gneissosity comprising strong cataclasis and mylonitization, penetrative planar and linear structures, and crystallization of muscovite and biotite in the foliation planes. New radiometric ages indicate that the deformation followed the crystallization of the batholith so closely that the K-Ar dating method cannot distinguish a difference, whereas previously published ages from the gneisses indicate a short time between the two events.

Arizona↗
USGS1976

Halogen contents of igneous minerals as indicators of magmatic evolution of rocks associated with the Ray porphyry copper deposit, Arizona

The contents of Cl, F, and H 2 O+ (calculated) in some hydrous igneous minerals in intrusive rocks of Laramide age (70-60 m.y.) near Ray, Ariz., appear to be related to the age and the chemistry of the whole-rock samples. Apatite and biotite in younger, more silicic rocks contain more F but less Cl and H 2 O+ than apatite and biotite in older, more mafic rock; the same relations hold for F and H 2 O+ in sphene. Correlations of the abundance of Cl, F, and H 2 O+ in hornblende with rock chemistry and age are not as strong as for apatite, biotite, and sphene; igneous (?) epidote does not contain Cl and F in amounts detectable by electron microprobe analysis. The contents of Cl, F, and H 2 O+ in whole-rock samples decrease with increasing differentiation index and decreasing age. Data for a single pluton of variable composition mirror the results for a suite of different plutons and dikes. The data are satisfactorily although not exclusively explained by postulating that the melts each contained progressively less Cl, F, and H 2 O and that the hydrons minerals consumed most of the Cl, F, and H 2 O in the magmas. The data may also be explained by postulating that (1) the stocks evolved Cl-bearing water during their ascent and crystallization, or that (2) Cl and H 2 O were concentrated during differentiation of the stocks but the minerals failed to record their buildup. Both alternative explanations find problems with and require special conditions to satisfy field, chemical, and experimental data. If many of the special conditions are not met, a nearby batholithic parent to the stocks is not a favorable source of the mineralized fluids at Ray. Propylitic alteration of biotite results in Cl-poor chlorites and may have provided some Cl to hydrothermal fluids; biotite may have also supplied some F to propylitizing fluids through alteration.

Arizona↗
USGS1974

Distribution of copper in biotite and biotite alteration products in intrusive rocks near two Arizona porphyry copper deposits

Biotite and its alteration products (primarily chlorite) from igneous rocks around the Ray and Esperanza (Esperanza-Sierrita) porphyry copper deposits, Arizona, were analyzed for copper by electron microprobe. The copper occurs in amounts >90 p/m (limit of detection) in most of the chlorites analyzed, is concentrated at the optical and chemical boundary of chlorite and biotite, and is not associated with sulfur. Most unaltered igneous and hydrothermal biotites analyzed contain <90 p/m Cu, and except for one sample, all copper that was detected can be explained as contamination by copper from chlorite grains. The paucity of detectable copper in igneous and hydrothermal biotite and its presence in daughter chlorite suggest that the positive association noted by some workers between the proximity of an ore deposit and the copper content of biotite might be partly the result: of increased amounts of chloritization of biotite near a deposit coupled with difficulty in physically cleaning the biotite separates. Additionally, previous speculations that (1) part of the copper in a deposit may come from altered biotite, and (2) copper in biotite indicates how copper behaves in a differentiating magma, are of doubtful value if based on data derived from analyses of bulk mineral separates.

Arizona↗
USGS1970

Nature and origin of early and late cherts in the Leadville Limestone, Colorado

Two generations of chert have been observed in the Mississippian Leadville Limestone of west-central Colorado: (1) an early chert inferred to have precipitated from hypersaline marine waters of high pH after those waters seeped into carbonate muds prior to final burial and lithification of the carbonate; and (2) a late chert that appears to have precipitated from ground waters as amorphous silica after initial lithification but prior to or during karst erosion of the formation in Late Mississippian (?) and Early Pennsylvanian time. A third type of microcrystalline quartz, hydrothermal jasperoid, is associated with ore deposits of Laramide age in the Leadville, but it is not discussed here. Conditions in west-central Colorado at the time that the early cherts formed in the Leadville were probably similar to those associated with the formation of early diagenetic chert in modern sediments, and the early chert in the Leadville is believed to have formed in a manner similar to the modern early cherts. The silica of the late chert appears to have come from Paleozoic sandstones below the Leadville. It was carried by slightly acid artesian waters into the formation, probably in concentrations of less than 60 ppm SiO 2 Super-saturation of amorphous silica occurred within the Leadville and probably was obtained by evaporative concentration at the water-air interface during dry seasons. Dissolution of the limestone by the slightly acid waters may account for the removal of the calcite that is replaced by chert.

Colorado↗