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David R. Wones

Publications and source records attributed to David R. Wones.

8 recordsLinked to original sources

Nomenclature of the micas

End-members and species defined with permissible ranges of composition are presented for the true micas, the brittle micas, and the interlayer-deficient micas. The determination of the crystallochemical formula for different available chemical data is outlined, and a system of modifiers and suffixes is given to allow the expression of unusual chemical substitutions or polytypic stacking arrangements. Tables of mica synonyms, varieties, ill-defined materials, and a list of names formerly or erroneously used for micas are presented. The Mica Subcommittee was appointed by the Commission on New Minerals and Mineral Names of the International Mineralogical Association. The definitions and recommendations presented were approved by the Commission.

Mineralogical Magazine

Lithotectonic assemblages as portrayed on the new bedrock geologic map of Massachusetts.

Scale of 1:250,000. The map units are grouped into eight lithotectonic packages. Five "zones" of older rocks that cover the whole state are, from west to east, the Taconic-Berkshire, Rowe-Hawley, Bronson Hill, Nashoba, and Milford-Dedham. In central and western Massachusetts, these zones are overlain by the Connecticut Valley and Merrimack "belts" of Silurian-Devonian, and local Carboniferous, strata; the two belts are distinguished from each other on the basis of the lithofacies of the Silurian strata. In eastern Massachusetts, the Milford-Dedham Zone also includes Silurian-Devonian, Carboniferous, Mesozoic, and Tertiary strata. A Mesozoic "basin" is separately identified in the Connecticut Valley region

Massachusetts

Oxidation during magmatic differentiation, Finnmarka Complex, Oslo area, Norway: Part 2, the mafic silicates

Electron-microprobe analyses are presented for pyroxene, amphibole, and biotite from monzonite, granodiorite, and granite at Finnmarka, Norway. Compositional trends measured in biotite, present in all three rock types, and in amphibole, present in the monzonite and granodiorite, are markedly atypical and are interpreted as reflecting crystallization under progressively more oxidizing conditions. The average Fe/Fe + Mg for biotites from successively more silicic rock types changes from 0.64 → 0.35 → 0.28, and for amphiboles changes from 0.58 in the monzonite to 0.29 in the granodiorite. Analyses of selected areas within amphibole grains in the granodiorite show marked chemical variations, although single-crystal X-ray photographs are sharp and do not reveal multiple phases. On the basis of 33 such analyses, four coupled substitutions are identified as operative; the most unusual finding is the relation of 1 Ti cation to 4 Al IV cations in the unit cell. Variations within individual amphibole grains of the granodiorite resemble changes noted in evolution of amphibole composition from monzonite to granodiorite and are interpreted as reflecting progressive oxidation. Consideration of these data for the mafic silicates, data for the opaque oxides, and the extensive formation of sphene in the granodiorite, has allowed development of schematic reactions and an overall picture of magmatic environment and evolution at Finnmarka. Crystallization apparently took place at PH 2 o of 1000 bars or less and a temperature of about 700 °C. The trend of oxidation during differentiation is more extreme than any heretofore reported. Amphiboles, as well as biotites, may participate in oxidation reactions and may reflect the oxidation-reduction processes that occurred during magmatic evolution.

Oslo

Properties of synthetic triclinic KFeSi3O8, iron-microcline, with some observations on the iron-microcline⇌iron-sanidine transition

Triclinic KFeSi 3 O 8 , iron-microcline, has been synthesized from oxide mixes and by complete conversion of monoclinic KFeSi 3 O 8 , iron-sanidine. Iron-microcline is triclinic, C ī, a =8·68±0·01 Å, b =13·10±0·01, c =7·34±0·01, α =90° 45′±10′, β =116° 03′±10′, γ=86°14′±10′. The optical properties (Na light) are: α =1·585±0·002, β =1·596±0·002, γ=1·605±0·002, 2 V α =85° (calc.), X≈ b , Z ∧ c =20°±5°. A reversible phase transition between triclinic and monoclinic KFeSi 3 O 8 occurs at 704°±6° C at 2000 bars total pressure. Iron-microcline is the low-temperature polymorph; no intermediate polymorphs were observed in either hydrothermal or dry heating experiments.

Journal of Petrology

The atomic ratios of natural ferruginous biotites with reference to 'the stability relations of the ferruginous biotite, annite'

The atomic ratios given by Eugster and Wones (1962) for analyses of high FeO-low MgO micas cited by Foster (1960) are in error. The recalculated atomic ratios herein presented show that only three of the thirteen have low (OH+F), and only one has characteristics that may possibly be due to loss of water during determination. None of the analyses exhibit characteristics suggestive of oxidation of iron and loss of H, as in progression towards oxyannite. The average recalculated octahedral occupancy is 2.69, not 2.91 as in the previous calculation. The differences between atomic ratios calculated on the basis ot determined H 2 O + and F and those calculated on the basis of the theoretical O 10 (OH) 2 content are not great enough to change the essential compositional character of these micas as interpreted by Foster (1960). However, they do affect significantly the calculated octahedral occupancy.

Journal of Petrology