Geology topics
L.E. Apodaca
Publications and source records attributed to L.E. Apodaca.
Peat
In 2012, domestic production of peat, excluding Alaska, was estimated to be 560 kt (617,000 st), compared with 568 kt (626,000 st) in 2011. In 2012, imports decreased to 940 kt (1 million st) compared with 982 kt (1.1 million st) in 2011, and exports were estimated to have increased to 75 kt (82,600 st) in 2012. U.S. apparent consumption for 2012 was estimated to have remained the same as that of 2011. World production was estimated to be about 27 Mt (30 million st) in 2012, which was slightly higher than 2011.
Sulfur
In 2011, elemental sulfur and the byproduct sulfuric acid were produced at 109 operations in 29 states and the U.S. Virgin Islands. Total shipments were valued at about $1.6 billion. Elemental sulfur production was 8.2 Mt (9 million st); Louisiana and Texas accounted for about 53 percent of domestic production.
Peat
In 2011, domestic production of peat, excluding Alaska, was estimated to be 605 kt (667,000 st), compared with 628 kt (629,000 st) in 2010. In 2011, imports increased to 1.1. Mt (1.2 million st) compared with 947 kt (1 million st) in 2010, and exports were estimated to have decreased to 39 kt (43,000 st) in 2011. U.S. apparent consumption for 2011 was estimated to have increased to 1.6 Mt (1.7 million st). World production was estimated to be about 22 Mt (24 million st) in 2011, which was 6 percent lower than 2010.
Nitrogen
Ammonia was produced by 12 companies at 27 plants in 15 states in the United States during 2011. Sixty-one percent of total U.S. ammonia production capacity was centered in Louisiana, Oklahoma and Texas because of those states' large reserves of natural gas, the dominant domestic feedstock. In 2011, U.S. producers operated at about 84 percent of their rated capacity (excluding plants that were idle for the entire year). Four companies — CF Industries Holdings Inc.; Koch Nitrogen Co.; PCS Nitrogen Inc. and Agrium Inc., in descending order — accounted for 77 percent of the total U.S. ammonia production capacity.
Peat
In 2010, domestic production of peat, excluding Alaska, was estimated to be 612 kt (674,600 st), compared with 609 kt (671,300 st) in 2009. In 2010, imports increased to 947 kt (1.04 million st), compared with 906 kt (998,600 st) in 2009. Exports were estimated to have decreased to 69 kt (76,000 st) in 2010. U.S. apparent consumption for 2010 was estimated to have increased to 1.5 Mt (1.65 million st). World production was estimated to be about 23 Mt (25 million st) in 2010, which is 8 percent lower than in 2009.
Nitrogen
Ammonia was produced by 12 companies at 24 plants in 16 states in the United States during 2010. Sixty percent of total U.S. ammonia production capacity was centered in Louisiana, Oklahoma and Texas because of those states' large reserves of natural gas, the dominant domestic feedstock.
Peat
In 2009, domestic production of peat, excluding Alaska, was estimated to be 610 kt (672,000 st), compared with 615 kt (678,000 st) in 2008. In 2009, imports decreased to 906 kt (999,000 st) compared with 936 kt (1 million st) in 2008, and exports were estimated to have increased to 77 kt (85,000 st) in 2009. U.S. apparent consumption for 2009 was estimated to be about the same as in 2008. World production was estimated to be about 25 Mt (27.5 million st) in 2009, which is about the same as 2008.
Nitrogen
Ammonia was produced by 13 companies at 23 plants in 16 states during 2009. Sixty percent of all U.S. ammonia production capacity was centered in Louisiana. Oklahoma and Texas because of those states' large reserves of natural gas, the dominant domestic feedstock. In 2009, U.S. producers operated at about 83 percent of their rated capacity (excluding plants that were idle for the entire year). Five companies — Koch Nitrogen Co.; Terra Industries Inc.; CF Industries Inc.; PCS Nitrogen Inc. and Agrium Inc., in descending order — accounted for 80 percent of the total U.S. ammonia production capacity. U.S. production was estimated to be 7.7 Mt (8.5 million st) of nitrogen (N) content in 2009 compared with 7.85 Mt (8.65 million st) of N content in 2008. Apparent consumption was estimated to have decreased to 12.1 Mt (13.3 million st) of N, a 10-percent decrease from 2008. The United States was the world's fourth-ranked ammonia producer and consumer following China, India and Russia. Urea, ammonium nitrate, ammonium phosphates, nitric acid and ammonium sulfate were the major derivatives of ammonia in the United States, in descending order of importance.
Occurrence, transport, and fate of trace elements, Blue River Basin, Summit County, Colorado: an integrated approach
Mining activities in the Blue River Basin, Summit County, Colorado, have affected the trace-element chemistry and biota along French Gulch and the Blue River. Elevated concentrations of As, Cd, Cu, Pb, and Zn were present in the bed and suspended sediments. Bed sediment trace-element concentrations were high in the streams in and near mining activities in the basin and remained high as water flowed into Dillon Reservoir about 3.5 km downstream. Bed-sediment (< 63 μm) data were useful in assessing the distribution of trace elements in the basin. Suspended-sediment measurements provided information as to the transport of the trace elements. Filtered (< 0.45 μm) water-column trace-element concentrations were orders of magnitude less than the sediment concentrations. Concentrations of Cd and Zn in the water column at some sites exceeded stream water-quality standards. Elevated trace-element concentrations in the sediment and water column are a source of contamination and must be considered in water-quality management of the Blue River Basin.
Analysis of ground-water-quality data of the Upper Colorado River basin, water years 1972-92
As part of the U.S. Geological Survey's National Water-Quality Assessment program, an analysis of the existing ground-water-quality data in the Upper Colorado River Basin study unit is necessary to provide information on the historic water-quality conditions. Analysis of the historical data provides information on the availability or lack of data and water-quality issues. The information gathered from the historical data will be used in the design of ground-water-quality studies in the basin. This report includes an analysis of the ground-water data (well and spring data) available for the Upper Colorado River Basin study unit from water years 1972 to 1992 for major cations and anions, metals and selected trace elements, and nutrients. The data used in the analysis of the ground-water quality in the Upper Colorado River Basin study unit were predominantly from the U.S. Geological Survey National Water Information System and the Colorado Department of Public Health and Environment data bases. A total of 212 sites representing alluvial aquifers and 187 sites representing bedrock aquifers were used in the analysis. The available data were not ideal for conducting a comprehensive basinwide water-quality assessment because of lack of sufficient geographical coverage. Evaluation of the ground-water data in the Upper Colorado River Basin study unit was based on the regional environmental setting, which describes the natural and human factors that can affect the water quality. In this report, the ground-water-quality information is evaluated on the basis of aquifers or potential aquifers (alluvial, Green River Formation, Mesaverde Group, Mancos Shale, Dakota Sandstone, Morrison Formation, Entrada Sandstone, Leadville Limestone, and Precambrian) and land-use classifications for alluvial aquifers. Most of the ground-water-quality data in the study unit were for major cations and anions and dissolved-solids concentrations. The aquifer with the highest median concentrations of major ions was the Mancos Shale. The U.S. Environmental Protection Agency secondary maximum contaminant level of 500 milligrams per liter for dissolved solids in drinking water was exceeded in about 75 percent of the samples from the Mancos Shale aquifer. The guideline by the Food and Agriculture Organization of the United States for irrigation water of 2,000 milligrams per liter was also exceeded by the median concentration from the Mancos Shale aquifer. For sulfate, the U.S. Environmental Protection Agency proposed maximum contaminant level of 500 milligrams per liter for drinking water was exceeded by the median concentration for the Mancos Shale aquifer. A total of 66 percent of the sites in the Mancos Shale aquifer exceeded the proposed maximum contaminant level. Metal and selected trace-element data were available for some sites, but most of these data also were below the detection limit. The median concentrations for iron for the selected aquifers and land-use classifications were below the U.S. Environmental Protection Agency secondary maximum contaminant level of 300 micrograms per liter in drinking water. Median concentration of manganese for the Mancos Shale exceeded the U.S. Environmental Protection Agency secondary maximum contaminant level of 50 micrograms per liter in drinking water. The highest selenium concentrations were in the alluvial aquifer and were associated with rangeland. However, about 22 percent of the selenium values from the Mancos Shale exceeded the U.S. Environmental Protection Agency maximum contaminant level of 50 micrograms per liter in drinking water. Few nutrient data were available for the study unit. The only nutrient species presented in this report were nitrate-plus-nitrite as nitrogen and orthophosphate. Median concentrations for nitrate-plus-nitrite as nitrogen were below the U.S. Environmental Protection Agency maximum contaminant level of 10 milligrams per liter in drinking water except for 0.02 percent of the sites in the alluvial aquifer and 0.03 percent of the sites in the Mancos Shale. Concentrations of orthophosphate did not vary significantly among aquifers or land-use classifications. Historic water-quality data from wells and springs helped to characterize the regional distribution of ground-water quality information in the Upper Colorado River Basin study unit. The historical ground-water data summarized in this report will be used in the design of a ground-water-quality network. Because ground-water-quality issues in the study unit are related to high dissolved solids, sulfate, selenium, and nutrients, this report discusses some of the important findings related to these issues.
Evidence for hot Mississippi Valley-type brines in the Reelfoot Rift complex, south-central United States, in Late Pennsylvanian-Early Permian
Petrographic and fluid inclusion studies of sparry dolomite cement from Upper Cambrian to Lower Ordovician rocks and conodont thermal-alteration indices provide evidence that hot mississippi valley-type brines were once present in the Reelfoot Rift complex. The cathodoluminescent microstratigraphy of sparry dolomite cement in the Reelfoot Rift resembles that of sparry dolomite cement associated with widespread mississippi valley-type deposition in the Ozark region. If correlative cathodoluminescent zones in the sparry dolomite from the Ozark and Reelfoot Rift regions indicate broadly contemporaneous dolomite deposition, then the results show that the Ozark MVT-type hydrothermal system extended into the Reelfoot region and onto the western flank of the Nashville Dome. Independent evidence supports migration of MVT-type brines into the Ozark region from the Reelfoot Rift complex in late Paleozoic time.
Fluid-inclusion gases in sphalerite, galena, and dolomite from the Silesian-Cracow Zn-Pb district, Poland
The gases in fluid inclusions from samples of sphalerite, galena, and sparry dolomite from ore deposits in the Silesian-Cracow zinc-lead district were determined by mass spectrometry. The results show that CO2 is the major gas in the fluid inclusions with lesser amounts of CH4. Samples of galena and sphalerite also commonly contain H2S and short-chain hydrocarbon gases. Gases in sphalerite and galena appear to contain two end-member compositions, CO2-CH4 and CO2-H2S bearing fluid inclusions. The apparent end member compositions could represent chemically distinct generations of fluid inclusions trapped at different times or at least two distinct fluids present during ore formation. The presence of distinct fluid inclusion gas compositions is consistent with previous fluid inclusion studies that show the presence of multiple fluids during ore deposition. The presence of multiple fluids in the ore-forming environment could lead to ore precipitation through processes of fluid mixing.
Bibliography, indices, and data sources of water-related studies, upper Colorado River basin, Colorado and Utah, 1872-1995
As part of the U.S. Geological Survey's National Water-Quality Assessment Program, current water-quality conditions in the Upper Colorado River Basin in Colorado and Utah are being assessed. This report is an initial effort to identify and compile information on water-related studies previously conducted in the basin and consists of a bibliography, coauthor and subject indices, and sources of available water-related data. Computerized literature searches of scientific data bases were carried out to identify past water-related studies in the basin, and government agencies and private organizations were contacted regarding their knowledge or possession of water-related publications and data. Categories of information in the bibliography include: aquatic biology, climate, energy development, geology, land use, limnology, runoff, salinity, surface- and ground-water hydrology, water chemistry, water quality and quantity, and water use and management. The approximately 1,400 indexed references date from 1872 through February 1995 and include books, journal articles, maps, and reports. In many instances, an abstract has been provided for a given reference. Sources of water-related data in the basin are included in a table.