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J.E. Taggart

Publications and source records attributed to J.E. Taggart.

10 recordsLinked to original sources
USGS2018

A reexamination of the turquoise group: The mineral aheylite, planerite (redefined), turquoise and coeruleolactite

The turquoise group has the general formula: A (sub 0-1) B 6 (PO 4 ) (sub 4-x) (PO 3 OH) x (OH) 8 .4H 2 O, where x = 0-2, and consists of six members: planerite, turquoise, faustite, aheylite, chalcosiderite and an unnamed Fe (super 2+) -Fe (super 3+) analogue. The existence of "coeruleolactite" is doubtful. Planerite is revalidated as a species and is characterized by a dominant A-site vacancy. Aheylite is established as a new member of the group, and is characterized by having Fe (super 2+) dominant in the A-site. Chemical analyses of 15 pure samples of microcrystalline planerite, turquoise, and aheylite show that a maximum of two of the (PO 4 ) groups are protonated (PO 3 OH) in planerite. Complete solid solution exists between planerite and turquoise. Other members of the group show variable A-site vacancy as well. Most samples of "turquoise" are cation-deficient or are planerite. Direct determination of water indicates that there are 4 molecules of water. Planerite, ideally []Al 6 (PO 4 ) 2 (PO 3 OH) 2 (OH) 8 .4H 2 O, is white, pale blue or pale green, and occurs as mamillary, botryoidal crusts as much as several mm thick; may also be massive; microcrystalline, crystals typically 2-4 micrometres, luster chalky to earthy, H. 5, somewhat brittle, no cleavage observed, splintery fracture, D m 2.68(2), D c 2.71, not magnetic, not fluorescent, mean RI about 1.60. a 7.505(2), b 9.723(3), c 7.814(2) Aa, alpha 111.43 degrees , beta 115.56 degrees , Gamma 68.69 degrees , V 464.2(1) Aa 3 , Z = 1. Aheylite, ideally Fe (super 2+) Al 6 (PO 4 ) 4 (OH) 8 .4H 2 O, is pale blue or green, and occurs as isolated and aggregate clumps of hemispherical or spherical, radiating to interlocked masses of crystals that average 3 micrometres in maximum dimension; porcelaneous-subvitreous luster, moderate to brittle tenacity, no cleavage observed, hackly to splintery fracture, not magnetic, not fluorescent, biax. (+), mean RI is about 1.63, D m 2.84(2), D c 2.90. a 7.400(1), b 9.896(1), c 7.627(1) Aa, alpha 110.87 degrees , beta 115.00 degrees , gamma 69.96 degrees , V 460.62(9) Aa 3 , Z = 1.

Mineralogical Magazine↗
USGS2008

The metallogeny of Late Triassic rifting of the Alexander terrane in southeastern Alaska and northwestern British Columbia

A belt of unusual volcanogenic massive sulfide (VMS) occurrences is located along the eastern margin of the Alexander terrane throughout southeastern Alaska and northwestern British Columbia and exhibits a range of characteristics consistent with a variety of syngenetic to epigenetic deposit types. Deposits within this belt include Greens Creek and Windy Craggy, the economically most significant VMS deposit in Alaska and the largest in North America, respectively. The occurrences are hosted by a discontinuously exposed, 800-km-long belt of rocks that consist of a 200- to 800-m-thick sequence of conglomerate, limestone, marine elastic sedimentary rocks, and tuff intercalated with and overlain by a distinctive unit of mafic pyroclastic rocks and pillowed flows. Faunal data bracket the age of the host rocks between Anisian (Middle Triassic) and late Norian (late Late Triassic). This metallogenic belt is herein referred to as the Alexander Triassic metallogenic belt. The VMS occurrences show systematic differences in degree of structural control, chemistry, and stratigraphic setting along the Alexander Triassic metallogenic belt that suggest important spatial or temporal changes in the tectonic environment of formation. At the southern end of the belt, felsic volcanic rocks overlain by shallow-water limestones characterize the lower part of the sequence. In the southern and middle portion of the belt, a distinctive pebble conglomerate marks the base of the section and is indicative of high-energy deposition in a near slope or basin margin setting. At the northern end of the belt the conglomerates, limestones, and felsic volcanic rocks are absent and the belt is composed of deep-water sedimentary and mafic volcanic rocks. This northward change in depositional environment and lithofacies is accompanied by a northward transition from epithermal-like structurally controlled, discontinuous, vein- and pod-shaped, Pb-Zn-Ag-Ba-(Cu) occurrences with relatively simple mineralogy, to sulfosalt-enriched VMS occurrences exhibiting characteristics of vein, diagenetic replacement, and exhalative styles of mineralization, and finally to Cu-Zn-(Co-Au) occurrences with larger and more clearly stratiform orebody morphologies. Occurrences in the middle of the belt are transitional in nature between structurally controlled types of mineralization that formed in a shallow-water, near-arc setting, to those having a more stratiform appearance, formed in a deeper water, rift-basin setting. The geologic setting in the south is consistent with shallow subaqueous emplacement on the flanks of the Alexander terrane. Northward, the setting changes to an increasingly deeper back- or intra-arc rift basin. Igneous activity in the Alexander Triassic metallogenic belt is characterized by a bimodal suite of volcanic rocks and a previously unrecognized association with mafic-ultramafic hypabyssal intrusions. Immobile trace and rare earth element (BEE) geochemical data indicate that felsic rocks in the southern portion of the belt are typical calc-alkaline rhyolites, which give way in the middle of the belt to peralkaline rhyolites. Rhyolites are largely absent in the northern part of the belt. Throughout the belt, the capping basaltic rocks have transitional geochemical signatures. Radiogenic isotope data for these rocks are also transitional (basalts and gabbros: ??-Nd = 4-9 and 87Sr/86Sr initial at 215 Ma = 0.7037-0.7074). Together these data are interpreted to reflect variable assimilation of mature island-arc crust by more primitive melts having the characteristics of either mid-ocean ridge (MORB) or intraplate (within-plate) basalts (WPB). The ore and host-rock geochemistry and the sulfosalt-rich mineralogy of the deposits are strikingly similar to recent descriptions of active sea-floor hydrothermal (white smoker) systems in back arcs of the southwest Pacific Ocean. These data, in concert with existing faunal ages, record the formation of a belt of VMS deposits

Conference Paper↗
USGS2008

Major and EDXRF Trace Element Chemical Analyses of Volcanic Rocks from Lassen Volcanic National Park and Vicinity, California

This open-file report presents WDXRF major-element chemical data for late Pliocene to Holocene volcanic rocks collected from Lassen Volcanic National Park and vicinity, California. Data for Rb, Sr, Ba, Y, Zr, Nb, Ni, Cr, Zn and Cu obtained by EDXRF are included for many samples. Data are presented in an EXCEL spreadsheet and are keyed to rock units as displayed on the Geologic Map of Lassen Volcanic National Park and vicinity (Clynne and Muffler, in press). Location of the samples is given in latitude and longitude in degrees and decimal minutes and in decimal degrees.

Open-File Report↗
USGS1991

Boromuscovite, a new member of the mica group, from the Little Three mine pegmatite, Ramona district, San Diego County, California

Boromuscovite, ideally KAl2(Si3B)O10(OH,F)2, in which [4]Al is replaced by B relative to muscovite, occurs as a late-stage, postpocket rupture mineral within the New Spaulding Pocket, main Little Three pegmatite dike. The mineral is white to cream colored and occurs as a porcelaneous veneer and coating on primary minerals. The average grain size is less than 3-4 ??m, but the coatings may be as much as 1 cm or more thick. Fragments of topaz, albite, elbaite, and other pocket minerals are included in the coating. The boromuscovite precipitated from a late-stage hydothermal fluid; it occurs only as a snowlike coating. Chemical composition, unit-cell parameters, Mohs hardness, cleavage, fracture, and optical properties are reported. -from Authors

American Mineralogist↗