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J.G. Crock

Publications and source records attributed to J.G. Crock.

At least 37 records · Page 2Linked to original sources

Analytical data for reconnaissance geochemical samples from mine dumps, stream sediments and waters at the Thompson Creek Tungsten Mine, Custer County, Idaho

The Thompson Creek mine is an inactive and abandoned tungsten mine located along Thompson Creek about 10.5 miles (17 km) northwest of Clayton, Idaho (see location map in file LOCATION.PDF). The mine consisted initially of open pit mining of outcrops and later of underground workings accessed by a single adit. The mine was worked through 1955 and waste piles presently reside in the flood plain above the east bank of Thompson Creek. A view of the collapsed adit is provided in the TIFF (Tagged-Image File Format) file ADIT.TIF (all photographs taken on 08/13/99). A south-facing view of the mine waste dumps is provided in the TIFF file SOUTH.TIF and a north-facing view is provided in NORTH.TIF.

Idaho

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

Rare earth elements in the phosphatic-enriched sediment of the Peru shelf

Apatite-enriched materials from the Peru shelf have been analyzed for their major oxide and rare earth element (REE) concentrations. The samples consist of (1) the fine fraction of sediment, mostly clay material, (2) phosphatic pellets and fish debris, which are dispersed throughout the fine-grained sediment, (3) tabular-shaped phosphatic crusts, which occur within the uppermost few centimeters of sediment, and (4) phosphatic nodules, which occur on the seafloor. The bulk REE concentrations of the concretions suggest that these elements are partitioned between the enclosed detrital material and the apatite fraction. Analysis of the fine-grained sediment with which the samples are associated suggested that this detrital fraction in the concretions should have shale REE values; the analysis of the fish debris suggested that the apatite fraction might have seawater values. The seawater contribution of REE's is negligible in the nodules and crust, in which the apatite occurs as a fine-grained interstitial cement. That is, the concentration of REE's and the REE patterns are predominantly a function of the amount of enclosed fine-grained sediment. By contrast, the REE pattern of the pelletal apatite suggests a seawater source and the absolute REE concentrations are relatively high. The REE P 2 O 5 "> REEP2O5 ratios of the apatite fraction of these samples thus vary from approximately zero (in the case of the crust and nodules) to as much as approximately 1.2 × 10 −3 (in the case of the pellets). The range of this ratio suggests that rather subtle variations in the depositional environment might cause a significant variation in the REE content of this authigenic fraction of the sediment.

Marine Geology