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R. A. Gulbrandsen

Publications and source records attributed to R. A. Gulbrandsen.

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The Phosphoria Formation at the Hot Springs Mine in Southeast Idaho: A source of selenium and other trace elements to surface water, ground water, vegetation, and biota

Major-element oxides and trace elements in the Phosphoria Formation at the Hot Springs Mine, Idaho were determined by a series of techniques. In this report, we examine the distribution of trace elements between the different solid components aluminosilicates, apatite, organic matter, opal, calcite, and dolomite that largely make up the rocks. High concentrations of several trace elements throughout the deposit, for example, As, Cd, Se, Tl, and U, at this and previously examined sites have raised concern about their introduction into the environment via weathering and the degree to which mining and the disposal of mined waste rock from this deposit might be accelerating that process. The question addressed here is how might the partitioning of trace elements between these solid host components influence the introduction of trace elements into ground water, surface water, and eventually biota, via weathering? In the case of Se, it is partitioned into components that are quite labile under the oxidizing conditions of subaerial weathering. As a result, it is widely distributed throughout the environment. Its concentration exceeds the level of concern for protection of wildlife at virtually every trophic level.

Idaho

Time and the crystallization of apatite in seawater

Carbonate fluorapatite has been synthesized in seawater in an experiment of nearly 10-years duration. The addition of phosphate to seawater whose fluoride concentration had been increased to 7.6 mg/l brought about an initial amorphous phosphate precipitate. After 20 months, a crystalline magnesium phosphate phase developed within the amorphous phosphate. Crystallization of apatite, which occurred during the last 3 years of the experiment, was accompanied by dissolution of the crystalline magnesium phosphate phase. The MgO content of the apatite (1.9 percent) is high in comparison to Tertiary and older apatite but similar to some young apatite; the CO 2 content (3.6 percent) is medium, and the fluorine content (2.2 percent) is low but again similar to some young apatite. The hydroxyl ion (OH − ) likely fills the need for additional fluorine-position atoms. The mole ratio of Ca plus substituent elements to P plus substituent elements (1.50) is low in comparison to the expected ratio of 1.67. The substitution of the hydronium ion (H 3 O + ) for Ca may account for this difference. The synthesis of apatite in seawater demonstrates that the factor of time overcomes the well known inhibiting effect of magnesium upon the crystallization of apatite. It also implies that given an adequate supply of phosphate, apatite can form in most ocean environments and likely plays a major pan in the control of the phosphate content of seawater.

Geochimica et Cosmochimica Acta

Whitlockite and apatite of surficial phosphate occurrences on Enderbury Island, Phoenix Islands, Pacific Ocean

Whitlockite and apatite are the principal phosphate minerals in the surficial deposits of Enderbury Island; monetite and brushite are present in small amounts. All are derived from the guano of sea birds. The abundance of whitlockite discovered on Enderbury, and reported in samples from Remire Island in the Indian Ocean, indicates that the mineral is probably of common occurrence in young insular phosphate deposits. The composition of whitlockite from Enderbury Island is roughly (Ca, Mg, Sr, Na) 3 (PO 4 , CO 3 ) 2 , similar to the composition indicated for other insular occurrences by the sparse data available. The variety of apatite found on the island is carbonate fluor-hydroxylapatite, low in fluorine content. Whitlockite appears to have formed directly from guano components in surficial aqueous solutions, possibly accompanied by apatite, but changes with time to apatite.

Enderbury Island, Phoenix Islands

Buddingtonite, ammonium feldspar, in the Phosphoria Formation, southeastern Idaho

Buddingtonite is distributed widely in the rocks of the Meade Peak Member of the Phosphoria Formation in southeastern Idaho and occurs in amounts up to about 50 percent. Most of the buddingtonite is in the middle mudstone interval of the member between two phosphate-rich intervals. The composition of the buddingtonite, in terms of a buddingtonite K-feldspar series, shows an apparent range of Bd 82 KF 18 to Bd 13 KF 87 , and compositions of Bd 72 KF 28 to Bd 50 KF 50 may be the most common. The predominant silicate mineral suite consists of buddingtonite-albite-illite. Albite is present in amounts up to about 20 percent. Buddingtonite may have developed directly from volcanic glass in the presence of abundant ammonium, derived from the decomposition of organic matter, in interstitial waters, or it may have formed at some later diagenetic stage from other products of volcanic glass alteration, such as montmorillonite or zeolites.

Idaho

Chemical composition of phosphorites of the Phosphoria Formation

The chemical composition, both major and minor constituents, of 60 samples of phosphorite from the Phosphoria Formation was determined. Major constituents of the average phosphorite are, by weight per cent: SiO 2 , 11·9; Al 2 O 3 , 1·7; Fe 2 O 3 ,1·1; MgO, 0·3; CaO, 44·0; Na 2 O, 0·6; K 2 O, 0·5; total H 2 O, 2·2; H 2 O − , 0·6; TiO 2 , 0·1; P 2 O 5 , 30·5; CO 2 , 2·2; SO 3 , 1·8; F, 3·1; organic matter, 2·1; and oil, 0·2. Uranium averages 0·009 per cent. The phosphate mineral is basically apatite, Ca 5 (PO 4 ) 3 F, with small but significant and variable substitutions—Na, Sr, U and Th for Ca, and CO 3 and SO 4 for PO 4 . Rare metals not associated with apatite are associated principally with the organic-matter component of the rocks. This group includes As, Ag, Cd, Cr, Cu, Mo, Ni, Sb, Se, V and Zn. Chromium is the most abundant, having a modal abundance of 0·1 per cent and a maximum concentration of 0·3 per cent. The average phosphorite is composed of approximately 80 per cent apatite, 10 per cent quartz, 5 per cent muscovite-illite, 2 per cent organic matter, 1 per cent dolomite—calcite, 1 per cent iron oxide, and 1 per cent other components. It is texturally a medium-grained pellet phosphorite.

Geochimica et Cosmochimica Acta

Glauconite from the Precambrian belt series, Montana

Glauconite from the upper part of the Missoula Group of the Belt Series, Flathead County, Montana, has been dated at 1070 million years by potassium-argon and rubidium-strontium analyses. This is the first glauconite of Precambrian age reported in North America.

Montana