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Find USGS publications on mineral resources and deposits. Search commodities and geographic names, then check source reports for geology and assessment methods.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data and is available at https://minerals.usgs.gov/minerals/pubs/mcs/ . Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for more than 90 individual minerals and materials.
This report is the earliest Government publication to furnish estimates covering 1995 nonfuel mineral industry data. Most of the estimates are based on at least 6 months of data. These data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials. Most data are rounded to no more than 3 significant figures.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Published on an annual basis, this report is the earliest Government publication to furnish estimates covering nonfuel mineral industry data. Data sheets contain information on the domestic industry structure, Government programs, tariffs, and 5-year salient statistics for over 90 individual minerals and materials.
Aeolian mineral dust is an important component of the Earth’s environmental systems, playing roles in the planetary radiation balance, as a source of fertilizer for biota in both terrestrial and marine realms and as an archive for understanding atmospheric circulation and paleoclimate in the geologic past. Crucial to understanding all of these roles of dust is the identification of dust sources. Here we review the methods used to identify dust sources active at present and in the past. Contemporary dust sources, produced by both glaciogenic and non-glaciogenic processes, can be readily identified by the use of Earth-orbiting satellites. These data show that present dust sources are concentrated in a global dust belt that encompasses large topographic basins in low-latitude arid and semiarid regions. Geomorphic studies indicate that specific point sources for dust in this zone include dry or ephemeral lakes, intermittent stream courses, dune fields, and some bedrock surfaces. Back-trajectory analyses are also used to identify dust sources, through modeling of wind fields and the movement of air parcels over periods of several days. Identification of dust sources from the past requires novel approaches that are part of the geologic toolbox of provenance studies. Identification of most dust sources of the past requires the use of physical, mineralogical, geochemical, and isotopic analyses of dust deposits. Physical properties include systematic spatial changes in dust deposit thickness and particle size away from a source. Mineralogy and geochemistry can pinpoint dust sources by clay mineral ratios and Sc-Th-La abundances, respectively. The most commonly used isotopic methods utilize isotopes of Nd, Sr, and Pb and have been applied extensively in dust archives of deep-sea cores, ice cores, and loess. All these methods have shown that dust sources have changed over time, with far more abundant dust supplies existing during glacial periods. Greater dust supplies in glacial periods are likely due to greater production of glaciogenic dust particles from expanded ice sheets and mountain glaciers, but could also include dust inputs from exposed continental and insular shelves now submerged. Future dust sources are difficult to assess, but will likely differ from those of the present because of global warming. Global warming could bring about shifts in dust sources by changes in degree or type of vegetation cover, changes in wind strength, and increases or decreases in the size of water bodies. A major uncertainty in assessing dust sources of the future is related to changes inhuman land use, which could affect land surface cover, particularly due to increased agricultural endeavors and water usage.
Zircon suites from the two main types of granite in the Granite Mountains, Wyoming, yielded concordia-intercept ages of 2,640??20 m.y. for a red, foliated granite (granite of Long Creek Mountain) and 2,595??40 m.y. for the much larger mass of the granite of Lankin Dome. These ages are statistically distinct (40??20 m.y. difference) and are consistent with observed chemical and textural differences. The lower intercepts of the zircon chords of 50??40 and 100+ 75 m.y. for the granite of Long Creek Mountain and granite of Lankin Dome, respectively, are not consistent with reasonable continuous diffusion lead-loss curves but do correspond well with the known (Laramide) time of uplift of the rocks. Epidote, zircon, and apatite from silicified and epidotized zones in the granites all record at least one postcrystallization disturbance in addition to the Laramide event and do not define a unique age of silicification and epidotization. The lower limit of ???2,500 m.y. provided by the least disturbed epidote, however, suggests that these rocks were probably formed by deuteric processes shortly after emplacement of the granite of the Lankin Dome. The earlier of the two disturbances that affected the minerals of the silicified-epidotized rock can be bracketed between 1,350 and 2,240 m.y. ago and is probably the same event that lowered mineral K-Ar and ages in the region. Zircon suites from both types of granite show well-defined linear correlations among U content, common-Pb content, and degree of discordance. One of the zircon suites has an extremely high common-Pb content (up to 180 ppm) and exhibits a component of radiogenic-Pb loss that is apparently unrelated to radiation damage. ?? 1978 Springer-Verlag.
Studies were conducted to determine whether interactions occur among dietary lysine, arginine and monovalent minerals in rainbow trout. In one experiment, rainbow trout fingerlings were fed diets containing three levels of lysine (2.4, 3.1 and 3.8 g per 100 g diet), two levels of arginine (1.7 and 2.5 g per 100 g diet) and two mixtures of Na + K + and Cl in a 3×2×2 factorial design. The mixtures varied in the proportions of cations to anions such that Cl equalled the sum of Na + and K + (cations − anions = 0 mEq/kg diet) in one mixture and exceeded the sum of Na + and K + (cations − anions = −200 mEq/kg diet) in the second mixture. Growth and efficiency of feed conversion were not affected by dietary lysine and arginine in fish fed diets containing − 200 mEq/kg balance, but when fish were fed diets containing a 0 mEq/kg balance, 3.8% lysine and a combination of 3.1% lysine and 2.5% arginine depressed both measures of response. Trout receiving the 0 mEq/kg cation-anion balance had significantly higher free histidine concentrations and lower free lysine concentrations in muscle and higher hepatic arginase activity (P≤0.01) than those receiving −200 mEq/kg. In another experiment, trout were fed diets containing three levels of K + (21, 191 and 360 mEq/kg), two levels of Na + (21 and 191 mEq/kg) and two levels of Cl − (179 and 347 mEq/kg) in a 3×2×2 factorial design. Growth and efficiency of feed conversion were depressed and hepatosomatic index increased with higher levels of dietary K + (P≤0.01), Na + (P≤0.05) and Cl (P≤0.01), with significant K + x Cl + (P≤0.01) and K + x Na + x Cl (P≤0.05) interactions. Increasing dietary K + resulted in increased levels of muscle free histidine and decreased levels of muscle free lysine and arginine (P≤0.01), while increasing dietary Cl increased muscle free lysine, the effect of which was dependent on dietary potassium (K + x Cl − , P≤0.01). It is concluded that dietary levels of K + , Na + and Cl − , irrespective of overall cation-anion balance of these minerals, affects growth rate, efficiency of feed utilization and the metabolism of basic amino acids in tissues of trout. Excess lysine causes depressed growth and efficiency of feed utilization. These effects were due to a lysine toxicity rather than a lysine-arginine antagonism, as they were not prevented by supplemental dietary arginine.
The Raman spectra of the natural end members of the garnet-group minerals, which include pyrope, almandine and spessarite of Fe-Al garnet series and grossularite, andradite and uvarovite of Ca-Fe garnet series, have been studied. Measured Raman spectra of these minerals are reasonably and qualitatively assigned to the internal modes, translational and rotatory modes of SiO 4 tetrahedra, as well as the translational motion of bivalent cations in the X site. The stretch and rotatory Al g modes for the Fe-Al garnet series show obvious Raman shifts as compared with those for the Ca-Fe garnet series, owing to the cations residing in the X site connected with SiO 4 tetrahedra by sharing the two edges. The Raman shifts of all members within either of the series are attributed mainly to the properties of cations in the X site for the Fe-Al garnet series and in the Y site for the Ca-Fe garnet series.
Previous studies have shown that sulfate-reduction activity occurs in a heterogeneous manner throughout the terrestrial subsurface. Low-activity regions are often observed in the presence of clay minerals. Here we report that clays inhibit sulfate reduction activity in sediments and in a pure culture of Desulfovibrio vulgaris . Clay minerals including bentonite and kaolinite inhibited sulfate reduction by 70–90% in sediments. Intact clays and clay colloids or soluble components, capable of passing through a 0.2-µm filter, were also inhibitory to sulfate-reducing bacteria. Other adsorbent materials, including anion or cation exchangers and a zeolite, did not inhibit sulfate reduction in sediments, suggesting that the effect of clays was not due to their cation-exchange capacity. We observed a strong correlation between the Al 2 O 3 content of clays and their relative ability to inhibit sulfate reduction in sediments ( r 2 = 0.82). This suggested that inhibition might be a direct effect of Al 3+ (aq) on the bacteria. We then tested pure aluminum oxide (Al 2 O 3 ) and showed it to act in a similar manner to clay. As dissolved aluminum is known to be toxic to a variety of organisms at low concentrations, our results suggest that the effects of clay on sulfate-reducing bacteria may be directly due to aluminum. Thus, our experiments provide an explanation for the lack of sulfate-reduction activity in clay-rich regions and presents a mechanism for the effect.