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M. Ross

Publications and source records attributed to M. Ross.

15 recordsLinked to original sources
USGS2018

Recommended nomenclature for zeolite minerals: Report of the subcommittee on zeolites of the International Mineralogical Association, Commission of New Minerals and Mineral Names

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission of New Minerals and Mineral Names. In a working definition of a zeolite mineral used for review, interrupted tetrahedral framework structures are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundance in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on Si:Al ratio except for heulandite (Si:Al < 4.0) and clinoptilolite ( Si : Al ⩾ 4.0 ). Dehydration, partial hydration, and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of a zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr.-Ba: chabazite-Ca.-Na.-K; clinoptilolite-K, -Na, -Ca: dachiardite-Ca, -Na; erionite-K, -Ca: faujasite-Na, -Ca, -Na: paulingite-K. -Ca; phillipsite-Na, -Ca, -Ka; stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data. IZA structure-type symbols, space-group symmetry; unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, svetlozarite, and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.

Mineralogical Magazine↗
USGS2005

Results of the acid rain program: Status and trends of emissions and environmental impacts (1990–2002)

Both SO2 and NOx emissions from power generation sources have significantly declined under Title IV. In 2002, SO2 emissions from Title IV-affected sources totaled 10.2 million tons and NOx emissions from all Title IV-affected sources totaled 4.5 million tons, down 35% and 33% respectively from 1990 levels. Sources in states with the highest emissions continue to reduce their emissions the most, and there have been no significant geographic shifts in emissions. The benefits of these emission reductions include improvements in air quality (which are expected to lead to significant human health benefits), broad-scale reductions in sulfate deposition, and improvements in visibility. While surface waters in some areas have begun to show signs of recovery from acidification, acidification is still occurring in many areas. Although there have been no broad-scale regional reductions in nitrogen deposition, nitrogen deposition has declined in some areas, benefiting some nitrogen-sensitive forests and coastal waters and acid-sensitive lakes and streams.

Book chapter↗
USGS2000

The crystal structure of tetranatrolite from Mont Saint-Hilaire, Quebec, and its chemical and structural relationship to paranatrolite and gonnardite

The structure of tetranatrolite from Mont Saint-Hilaire, Quebec (U.S. National Museum sample R1830) with a = 13.197(7) A, c = 6.630(9) A, and space group I42d, was refined using single-crystal X-ray data. A representative formula of tetranatrolite determined from electron microprobe analysis is Na12.50K0.01Ca2.93Sr0.11Al19.09 Si20.91O79.74??nH2O. The structure has the basic natrolite Si-Al-O framework configuration with Na, Ca, Sr, and K residing within inter-framework cages. Aluminum is disordered over the T1 and T2 tetrahedral sites, with T2 > T1. Water molecules O4 and O5 coordinate the intercage atoms and have high displacement parameters, indicating disorder within the cages. The Mont Saint-Hilaire tetranatrolite structure is compared to four previously determined structures, two tetranatrolite samples from Khibiny and Lovozero, Russia and two "gonnardite" samples from Tvedalen, Norway and Gignat, France. Observations are given to indicate that the Norwegian sample deduced to be tetranatrolite rather than gonnardite. Although the crystal structures of tetranatrolite and gonnardite are very similar, it is shown that the tetranatrolite compositions differ significantly from those of gonnardite. The tetranatrolite composition series varies along the join Na16Al16Si24O80-Na12 Ca4Al20Si20O80, and is represented by the formula Na16-xCaxAl16+xSi24-x O80??nH2O, where x extends from approximately 2.4 to 3.9. In contrast, gonnardites from Arkansas and Austria have compositions that vary along the join Na16Al16Si24O80-Na4 Ca8Al20Si20O80, which are represented by the formula ???xNa16-3xCa2xAl16+x Si24-xO80??nH2O and where ??? indicates vacant intercage cation sites and x varies from approximately 0.3 to 3.2. Tetranatrolite is a dehydration product of paranatrolite and probably does not have a true stability field.

American Mineralogist↗
USGS1998

Recommended nomenclature for zeolite minerals: Report of the Subcommittee on Zeolites of the International Mineralogical Association, Commission on New Minerals and Mineral Names

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is alloowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemical symbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely in Si:Al ratio except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration and over-hydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of zeolite. Newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba; chabazite-Ca, -Na, -K; clinoptilolite-K, -Na, -Ca; dechiardite-Ca, -Na; erionite-Na, -K, -Ca,; faujasite-Na, -Ca, -Mg; ferrierite-Mg, -K, -Na; gmelinite-Na, -Ca, -K; heulandite-Ca, -Na, -K, -Sr; levyne-Ca, -Na; paulingite-K, -Ca; phillipsite-Na, -Ca, -K stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, svetlozarite and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.

European Journal of Mineralogy↗
USGS1997

Recommended nomenclature for zeolite minerals: report of the subcommittee on zeolites of the International Mineralogical Association, Commission on new Minerals and Mineral names

This report embodies recommendations on zeolite nomenclature approved by the International Mineralogical Association, Commission on New Minerals and Mineral Names. In a working definition of a zeolite mineral used for this review, structures containing an interrupted framework of tetrahedra are accepted where other zeolitic properties prevail, and complete substitution by elements other than Si and Al is allowed. Separate species are recognized in topologically distinctive compositional series in which different extra-framework cations are the most abundant in atomic proportions. To name these, the appropriate chemicalsymbol is attached by a hyphen to the series name as a suffix, except for the names harmotome, pollucite and wairakite in the phillipsite and analcime series. Differences in space-group symmetry and in order-disorder relationships in zeolites having the same topologically distinctive framework do not in general provide adequate grounds for recognition of separate species. Zeolite species are not to be distinguished solely on the ratio Si:Al except for heulandite (Si:Al < 4.0) and clinoptilolite (Si:Al ??? 4.0). Dehydration, partial hydration, and overhydration are not sufficient grounds for the recognition of separate species of zeolites. Use of the term 'ideal formula' should be avoided in referring to a simplified or averaged formula of a zeolite. newly recognized species in compositional series are as follows: brewsterite-Sr, -Ba, chabazite-Ca, -Na, -K, clinoptilolite-K, -Na, -Ca, dachiardite-Ca, -Na, erionite-Na, erionite-Na, -K, -Ca, faujasite-Na, -Ca, -Mg, ferrierite-Mg, -K, -Na, gmelinite-Na, -Ca, -K, heulandite-Ca, -Na, -K, -Sr, levyne-Ca, -Na, paulingite-K, -Ca, phillipsite-Na, -Ca, -K, and stilbite-Ca, -Na. Key references, type locality, origin of name, chemical data, IZA structure-type symbols, space-group symmetry, unit-cell dimensions, and comments on structure are listed for 13 compositional series, 82 accepted zeolite mineral species, and three of doubtful status. Herschelite, leonhardite, dvetlozarite, and wellsite are discredited as mineral species names. Obsolete and discredited names are listed.

Canadian Mineralogist↗
USGS1992

Crystalline solution series and order-disorder within the natrolite mineral group

Electron microprobe and X-ray analyses were made of natrolite, tetranatrolite, gonnardite, and thomsonite from the Magnet Cove alkaline igneous complex, Arkansas, and of selected specimens from the U.S. National Museum. This information and data from the literature indicate that natrolite, mesolite, scolecite, edingtonite, and tetraedingtonite show only small deviations from the ideal stoichiometry. In contrast, gonnardite, tetranatrolite, and thomsonite show large deviations from the ideal end-member compositions and compose three crystalline series. The structures of the natrolite minerals are defined by combining each of the three types of framework structures with various combinations of channel-occupying polyhedra. Various polysomatic series can be constructed by combining slices of two basic structures to form new hybrid structures. -from Authors

American Mineralogist↗
USGS1990

Alkaline igneous rocks of Magnet Cove, Arkansas: Mineralogy and geochemistry of syenites

Syenites from the Magnet Cove alkaline igneous complex form a diverse mineralogical and geochemical suite. Compositional zoning in primary and late-stage minerals indicates complex, multi-stage crystallization and replacement histories. Residual magmatic fluids, rich in F, Cl, CO2 and H2O, reacted with primary minerals to form complex intergrowths of minerals such as rinkite, fluorite, V-bearing magnetite, F-bearing garnet and aegirine. Abundant sodalite and natrolite formed in pegmatitic segregations within nepheline syenite where Cl- and Na-rich fluids were trapped. During autometasomatism compatible elements such as Mn, Ti, V and Zr were redistributed on a local scale and concentrated in late-stage minerals. Early crystallization of apatite and perovskite controlled the compatible behavior of P and Ti, respectively. The formation of melanite garnet also affected the behaviour of Ti, as well as Zr, Hf and the heavy rare-earth elements. Pseudoleucite syenite and garnet-nepheline syenite differentiated along separate trends, but the two groups are related to the same parental magma by early fractionation of leucite, the presumed precursor of intergrowths of K-feldspar and nepheline. The Diamond Jo nepheline syenite group defines a different differentiation trend. Sphene-nepheline syenite, alkali syenite and several miscellaneous nepheline syenites do not consistently plot with the other syenite groups or each other on element and oxide variation diagrams, indicating that they were derived from still other parental syenite magmas. Mineral assemblages indicate that relatively high f{hook};O2, at or above the fayalite-magnetite-quartz buffer, prevailed throughout the crystallization history of the syenites. ?? 1990.

LITHOS↗
USGS1970

Cummingtonite: A reversible, nonquenchable transition from P21/m to C2/m symmetry

Cummingtonite from the Gouverneur, New York, talc district (Sample No. U.S.N.M. 115046) with the composition, (Ca 0.36 Na 0.06 Mn 0.96 Mg 0.57 ) Mg 5 Si 8 O 22 (OH) 2 , unit cell parametersa = 9.550 ± 0.001, b = 18.007 ± 0.003, c = 5.298 ± 0.001Å, β = 102°39′ ± 1′, and space groupP2 1 /m, has been used in a high-temperature, single-crystal, X-ray diffraction study. When diffraction patterns are taken of the crystals heated in a sealed silica capillary to 45°C or higher, these reflections disappear, indicating a transition toC2/m symmetry. The transition appears to be analogous to theP2 1 /ctoC2/c transition between 700° and 800°C discovered recently in (Mg 0.30 Fe 0.70 ) SiO 3 clinopyroxene. In addition to the cummingtonite transition, we have also found a transition in pigeonite at higher temperatures. The transition occurs in this pigeonite (Gunflint Iron Formation, Minnesota, (Ca 0.04 Fe 0.78 Mg 0.18 )SiO 3 ) at about 670°C. This is a significantly lower temperature than was found for the Ca-poor clinopyroxene.

Earth and Planetary Science Letters↗
USGS1970

Lunar clinopyroxenes: Chemical composition, structural state, and texture

Single-crystal x-ray diffraction, microprobe, optical and electron optical examinations of clinopyroxenes from Apollo 11 lunar samples 10003, 10047, 10050, and 10084 show that generally the crystals are composed of (001) augite-pigeonite intergrowths in varying ratios. Transmission electron micrographs reveal abundant exsolution lamellae, many only 60 Å thick. In addition to the phase inhomogeneities, primary chemical inhomogeneities are clearly demonstrated. There are reciprocal relationships between calcium and iron and between Ti 4+ + 2Al and R 2+ + 2Si. Our evidence suggests that a chemically inhomogeneous subcalcic C 2/ c augite was the only primary pyroxene from which pigeonite later exsolved.

Science↗
USGS1970

Deformation twins in Hornblende

Hornblende deformation twins with twin planes parallel to (¯101) are produced experimentally in single crystals by compression parallel to the c axis. Twinning occurs at confining pressures from 5 to 15 kilobars and temperatures from 400° to 600°C (strain rate, 10 -5 per second).

Science↗
USGS1969

Equilibrium coexistence of three amphiboles

Electron probe and wet chemical analyses of amphibole pairs from the sillimanite zone of central Massachusetts and adjacent New Hampshire indicated that for a particular metamorphic grade there should be a restricted composition range in which three amphiboles can coexist stably. An unequivocal example of such an equilibrium three amphibole rock has been found in the sillimanite-orthoclase zone. It contains a colorless primitive clinoamphibole, space group P 2 1 / m , optically and chemically like cummingtonite with blue-green hornblende exsolution lamellae on (100) and (¯101) of the host; blue-green hornblende, space group C2/m , with primitive cummingtonite exsolution lamellae on (100) and (¯101) of the host; and pale pinkish tan anthophyllite, space group Pnma , that is free of visible exsolution lamellae but is a submicroscopic intergrowth of two orthorhombic amphiboles. Mutual contacts and coarse, oriented intergrowths of two and three host amphiboles indicate the three grew as an equilibrium assemblage prior to exsolution. Electron probe analyses at mutual three-amphibole contacts showed little variation in the composition of each amphibole. Analyses believed to represent most closely the primary amphibole compositions gave atomic proportions on the basis of 23 oxygens per formula unit as follows: for primitive cummingtonite (Na 0.02 Ca 0.21 − Mn 0.06 Fe 2+ 2.28 Mg 4.12 Al 0.28 ) (Al 0.17 Si 7.83 ), for hornblende (Na 0.35 Ca 1.56 Mn 0.02 Fe 1.71 Mg 2.85 Al 0.92 ) (Al 1.37 Si 6.63 ), and for anthophyllite (Na 0.10 Ca 0.06 Mn 0.06 Fe 2.25 Mg 4.11 Al 0.47 ) (Al 0.47 Si 7.53 ). The reflections violating C -symmetry, on X-ray single crystal photographs of the primitive cummingtonite, are weak and diffuse, and suggest a partial inversion from a C -centered to a primitive clinoamphibole. Single crystal photographs of the anthophyllite show split reflections indicating it is an intergrowth of about 80% anthophyllite and about 20% gedrite which differ in their b crystallographic dimensions. Split reflections are characteristic of all analyzed orthorhombic amphiboles so far examined from Massachusetts and New Hampshire except the most aluminous gedrites, and the relative intensity of the gedrite reflections is roughly proportional to the degree of Na and Al substitution. Thin sections of a few of these anthophyllite specimens show lamellae parallel to (010) that are just resolved with a high power objective.

Contributions to Mineralogy and Petrology↗
USGS1968

Exsolution in clinoamphiboles

Ten amphibole specimens from a variety of metamorphic rocks such as talc schists, eclogites, and metamorphosed iron formations contain lamellae of a second amphibole oriented parallel to (1̅01) or (100), or both, of the host. Tremolites, actinolites, and hornblendes commonly have lamellae of a calcium-poor clinoamphibole with P 2 1 / m space-group symmetry, or lamellae of cummingtonite with C 2/ m space-group symmetry. Likewise cummingtonites and P 2 1 / m clinoamphiboles commonly contain lamellae of calcium-rich C 2/ m amphiboles such as tremolite. Results of x-ray diffraction, electron-probe, and microscope studies indicate that most lamellae result from unmixing of a homogeneous amphibole. The P 2 1 / m clinoamphibole is analogous to the clinopyroxene pigeonite in agreement with the results of M. G. Bown.

Science↗
USGS1966

Mica polytypes: Systematic description and identification

X-ray studies of mica specimens from a variety of geological localities show that biotite and certain lithium-rich mica samples are composed of a mixture of different polytypes. Many of the biotite structures are new complex polytypes not before reported. A new method of designating mica polytypes is proposed. Techniques are described for the systematic generation of all the possible layer-stacking sequences of mica polytypes and for the verification of the stacking sequences in newly discovered forms.

Science↗
USGS1960

The crystal structure of cesium biuranyl trisulphate, Cs2(UO2)2(SO4)3

The crystal structure of the new compound Cs(UO 2 ) 2 (SO 4 ) 3 has been determined by X-ray diffraction methods. The compound is tetragonal, space group P 4 2 1 m "> P42 1 m ( D 2 d 3 ), with a = 9·62 ± 0·02, c = 8&#xB7;13 &#xB1; 0&#xB7;01 A &#x30A; "> c = 8·13 ± 0·01Å , and Z = 2; s.g. (calc.) = 4·80 ± 0·03, s.g. (obs.) = 4·74 ± 0·05. The compound forms plates parallel to (001) bounded by the form (110). Intensity data were obtained from Buerger precession photographs of the ( hk 0) and (0 kl ) reciprocal lattice nets. No corrections for absorption were made. The co-ordinates of the U and Cs atoms were obtained by interpretation of the Patterson projections normal to (001) and (100) and a plausible structure was derived from electron density projections. The final parameters of the structure were determined from subtraction electron density maps, least squares analysis of the structure factors, and spatial considerations. The compound has a layer structure consisting of (UO 2 ) 2 (SO 4 ) 3 ] n 2 n − sheets paralle to (001), tied together by cesium ions. The UO 2 2+ group is co-ordinated by five sulphate oxygens which form a nearly plane pentagon approximately normal to the uranyl axis. The Cs 2 atom is co-ordinated by twelve oxygen atoms and the Cs 1 atom by eight oxygen atoms. X-ray and optical data are also given for the compound Rb 2 UO 2 (SO 4 ) 2 ·2H 2 O.

Journal of Inorganic and Nuclear Chemistry↗