Geology topics
Source-linked reports with geographic coverage including Puerto Rico, United States.
The Earth Mapping Resources Initiative is filling data gaps and fostering more holistic understanding of critical mineral resources in the United States using a novel mineral systems framework.
The Earth Mapping Resources Initiative (Earth MRI) is conducted in phases to identify areas for acquiring new geologic framework data to identify potential domestic resources of the 35 mineral materials designated as critical minerals for the United States. This report describes the data sources and summary results for 13 critical minerals evaluated in the conterminous United States and Puerto Rico during phase 3 of the study (antimony, barite, beryllium, chromium, fluorspar, hafnium, helium, magnesium, manganese, potash, uranium, vanadium, and zirconium). Phases 1 and 2 of the Earth MRI addressed aluminum, cobalt, graphite, lithium, niobium, platinum-group elements (PGEs), rare earth elements (REEs), tantalum, tin, titanium, and tungsten. Critical minerals in Alaska are covered in a separate report. No focus areas for phase 3 critical minerals are delineated for Hawaii. The geologic, geochemical, topographic, and geophysical mapping provided by the Earth MRI documents geologic features that reflect the extent of individual mineral systems and provides information about critical mineral deposits that may not have been previously considered. The mineral-systems approach links critical mineral commodities to deposit types that represent the manifestations of large mineral systems. Each of the 13 critical mineral commodities for phase 3 of the Earth MRI is discussed in terms of its importance to the Nation’s economy, modes of occurrence, mineral systems, and deposit types, and is accompanied by maps and tables listing examples of focus areas in the conterminous United States and Puerto Rico. Examples of important mineral systems for this group of 13 critical minerals include basin brine path systems for barite and fluorspar, Carlin-type systems and Coeur d’Alene systems for antimony, chemical weathering and volcanogenic seafloor systems for manganese, Climax-type systems for beryllium, mafic magmatic systems for chromium, marine evaporite systems for potash and magnesium, meteoric recharge systems for uranium, petroleum systems for helium, and placer systems for zirconium and hafnium.
Assessment and management of the risks of exposure to complex chemical mixtures in streams are priorities for human and environmental health organizations around the world. The current lack of information on the composition and variability of environmental mixtures and a limited understanding of their combined effects are fundamental obstacles to timely identification and prevention of adverse human and ecological effects of exposure. This report describes the design of a field-based study of the composition and biological activity of chemical mixtures in U.S. stream waters affected by a wide range of human activities and contaminant sources. The study is a collaborative effort by the U.S. Geological Survey and the U.S. Environmental Protection Agency. Scientists sampled 38 streams spanning 24 States and Puerto Rico. Thirty-four of the sites were located in watersheds impacted by multiple contaminant sources, including industrial and municipal wastewater discharges, crop and animal agricultural runoff, urban runoff, and other point and nonpoint contaminant sources. The remaining four sites were minimally development reference watersheds. All samples underwent comprehensive chemical and biological characterization, including sensitive and specific direct analysis for over 700 dissolved organic and inorganic chemicals and field parameters, identification of unknown contaminants (environmental diagnostics), and a variety of bioassays to evaluate biological activity and toxicity.
This report presents water-quality data from two nationwide studies on the occurrence and distribution of organic wastewater contaminants. These data are part of the continuing effort of the U.S. Geological Survey Toxic Substances Hydrology Program to collect baseline information on the environmental occurrence of pharmaceuticals and other organic wastewater contaminants. In 2000, samples were collected from 47 ambient ground-water sites (not drinking-water wells) in 18 states and analyzed for 65 organic wastewater contaminants. In the summer of 2001, samples were collected from 74 sources of raw, untreated, drinking water in 25 states and Puerto Rico and analyzed for 100 organic wastewater contaminants. These sources comprise 25 ground-water and 49 surface-water sources of drinking water serving populations ranging from one family to more than 8 million people. Site selection for both studies focused on areas known or suspected to contain sources of animal and/or human wastewater. The five most frequently detected compounds in samples collected from ambient ground-water sites are N,N-diethyltoluamide (35 percent, insect repellant), bisphenol A (30 percent, plasticizer), tri(2-chloroethy) phosphate (30 percent, fire retardant), sulfamethoxazole (23 percent, veterinary and human antibiotic), and 4-octylphenol monoethoxylate (19 percent, detergent metabolite). The five most frequently detected organic wastewater contaminants in samples of untreated drinking water from surface-water sources are cholesterol (59 percent, natural sterol), metolachlor (53 percent, herbicide), cotinine (51 percent, nicotine metabolite), β-sitosterol (37 percent, natural plant sterol), and 1,7-dimethylxanthine (27 percent, caffeine metabolite). The five most frequently detected organic wastewater contaminants in samples of untreated drinking water from ground-water sources are tetrachloroethylene (24 percent, solvent), carbamazepine (20 percent, pharmaceutical), bisphenol A (20 percent, plasticizer), 1,7-dimethylxanthine (16 percent, caffeine metabolite), and tri(2-chloroethyl) phosphate (12 percent, fire retardant).