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Structure maps and seismic stratigraphy of the Yakataga segment of the continental margin, northern Gulf of Alaska

Multichannel seismic-reflection data show the late Cenozoic structure, seismic stratigraphy, and geologic history of the Yakataga segment of the continental margin, between Icy Bay and Kayak Island, northern Gulf of Alaska. The structure of the Yakataga segment consists of broad folds and associated thrust faults beneath the continental shelf and slope, trending generally northeast in the eastern part of the s~gment to east-west in the western part. Anticlines are generally asymmetric and doubly plunging and are commonly bounded on the seaward side by high-angle thrust faults. The degree of deformation is less intense than is observed in adjacent onshore areas. The age of deformation decreases seaward and the deformation shows an overall southeastward migration with time. Structures of similar age define three structural zones; structural growth was roughly contemporaneous in each structural zone, although the local growth pattern is complex in detail. Deformation within each structural zone was followed by subsidence and burial by rapidly deposited marine sediment. Deformation appears to have been continuous during the late Cenozoic, rather than a series of discrete events, because subsidence of a particular structural zone is accompanied by initiation of growth on a younger, more seaward zone. Varying degrees of reactivation of the older structures within recent time have resulted in renewed uplift of these structures. Average sedimentation, uplift, and subsidence rates are all extremely high, and generally range from about 1 to 2 m/1,000 yr; these rates can locally be much higher. The average strike of structures in the Yakataga segment indicates northwest-southeastward compression and is consistent with the current convergence direction between the Pacific and North America plates. Observed shortening within the segment is much less than required by the late Cenozoic convergence rate (about 6 cm/yr), and the major deformation is taken up elsewhere, primarily onshore. Thus, the deformation of the Yakataga segment is caused by minor shortening of the continental margin between Cross Sound and Kayak Island, which together comprise the Yakutat block, as the margin moves northwestward with the Pacific plate and collides with the North America plate.

Alaska↗

ERF1_2 -- Enhanced River Reach File 2.0

The digital segmented network based on watershed boundaries, ERF1_2, includes enhancements to the U.S. Environmental Protection Agency's River Reach File 1 (RF1) (USEPA, 1996; DeWald and others, 1985) to support national and regional-scale surface water-quality modeling. Alexander and others (1999) developed ERF1, which assessed the hydrologic integrity of the digital reach traces and calculated the mean water time-of-travel in river reaches and reservoirs. ERF1_2 serves as the foundation for SPARROW (Spatially Referenced Regressions (of nutrient transport) on Watershed) modeling. Within the context of a Geographic Information System, SPARROW estimates the proportion of watersheds in the conterminous U.S. with outflow concentrations of several nutrients, including total nitrogen and total phosphorus, (Smith, R.A., Schwarz, G.E., and Alexander, R.B., 1997). This version of the network expands on ERF1 (Version 1.2; Alexander, et al., 1999) and includes the incremental and total drainage area derived from 1-kilometer (km) elevation data for North America. Previous estimates of the water time-of-travel were recomputed for reaches with water-quality monitoring sites that included two reaches. The mean flow and velocity estimates for these split reaches are based on previous estimation methods (Alexander et al., 1999) and are unchanged in ERF1_2. Drainage area calculations provide data used to estimate the contribution of a given nutrient to the outflow. Data estimates depend on the accuracy of node connectivity. Reaches split at water-quality or pesticide-monitoring sites indicate the source point for estimating the contribution and transport of nutrients and their loads throughout the watersheds. The ERF1_2 coverage extends the earlier drainage area founded on the 1-kilometer data for North America (Verdin, 1996; Verdin and Jenson, 1996). A 1-kilometer raster grid of ERF1_2 projected to Lambert Azimuthal Equal Area, NAD 27 Datum (Snyder, 1987), was merged with the HYDRO1K flow direction data set (Verdin and Jenson, 1996) to generate a DEM-based watershed grid, ERF1_2WS_LG. The watershed boundaries are maintained in a raster (grid cell) format as well as a vector (polygon) format for subsequent model analysis. Both the coverage, ERF1_2, and the grid, ERF1_2WS_LG, are available at: URL:http://water.usgs.gov/lookup/getspatial?erf1_2

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Sonoran Pronghorn Literature: An Annotated Bibliography

EXECUTIVE SUMMARY The Sonoran pronghorn (Antilocapra americana sonoriensis) is 1 of 5 subspecies of pronghorn in North America. Sonoran pronghorn historically ranged from eastern California into southeastern Arizona and south to Sonora, Mexico. Sonoran pronghorn currently inhabit the Sonoran Desert in Southwestern Arizona and northern Sonora, Mexico. Unfortunately, their future in North America is uncertain. In the United States, as of December 2004, there were <51 freeranging individual Sonoran pronghorn. This subspecies has been listed as endangered by the United States Fish and Wildlife Service since 1967. Because of the rapid decline in population size, biologists and managers increased management efforts to reverse the downward spiral to extinction. To assist with enhanced management we have compiled an annotated bibliography of most of the works published on Sonoran pronghorn including peer-reviewed papers (n = 31, including submitted manuscripts), books (n = 26), theses and dissertations (n = 5), conferences, proceedings and symposiums (n = 31), reports (n = 84), abstracts (n = 14), popular articles (n = 41), and others (n = 4). These are the same categories under which we list annotations. Most of the articles involve A. a. sonoriensis. We present the scientific name of other pronghorn when clarification is needed.

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Peru Mercury Inventory 2006

In 2004, a specific need for data on mercury use in South America was indicated by the United Nations Environmental Programme-Chemicals (UNEP-Chemicals) at a workshop on regional mercury pollution that took place in Buenos Aires, Argentina. Mercury has long been mined and used in South America for artisanal gold mining and imported for chlor-alkali production, dental amalgam, and other uses. The U.S. Geological Survey (USGS) provides information on domestic and international mercury production, trade, prices, sources, and recycling in its annual Minerals Yearbook mercury chapter. Therefore, in response to UNEP-Chemicals, the USGS, in collaboration with the Economic Section of the U.S. Embassy, Lima, has herein compiled data on Peru's exports, imports, and byproduct production of mercury. Peru was selected for this inventory because it has a 2000-year history of mercury production and use, and continues today as an important source of mercury for the global market, as a byproduct from its gold mines. Peru is a regional distributor of imported mercury and user of mercury for artisanal gold mining and chlor-alkali production. Peruvian customs data showed that 22 metric tons (t) of byproduct mercury was exported to the United States in 2006. Transshipped mercury was exported to Brazil (1 t), Colombia (1 t), and Guyana (1 t). Mercury was imported from the United States (54 t), Spain (19 t), and Kyrgyzstan (8 t) in 2006 and was used for artisanal gold mining, chlor-alkali production, dental amalgam, or transshipment to other countries in the region. Site visits and interviews provided information on the use and disposition of mercury for artisanal gold mining and other uses. Peru also imports mercury-containing batteries, electronics and computers, fluorescent lamps, and thermometers. In 2006, Peru imported approximately 1,900 t of a wide variety of fluorescent lamps; however, the mercury contained in these lamps, a minimum of approximately 76 kilograms (kg), and in other products such as batteries and computer electronics is not recycled and may ultimately be released to the environment.

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Compilation of surface creep on California faults and comparison of WGCEP 2007 deformation model to Pacific-North American plate Mmtion

This Appendix contains 3 sections that 1) documents published observations of surface creep on California faults, 2) constructs line integrals across the WG-07 deformation model to compare to the Pacific - North America plate motion, and 3) constructs strain tensors of volumes across the WG-07 deformation model to compare to the Pacific - North America plate motion. Observation of creep on faults is a critical part of our earthquake rupture model because if a fault is observed to creep the moment released as earthquakes is reduced from what would be inferred directly from the fault's slip rate. There is considerable debate about how representative creep measured at the surface during a short time period is of the whole fault surface through the entire seismic cycle (e.g. Hudnut and Clark, 1989). Observationally, it is clear that the amount of creep varies spatially and temporally on a fault. However, from a practical point of view a single creep rate is associated with a fault section and the reduction in seismic moment generated by the fault is accommodated in seismic hazard models by reducing the surface area that generates earthquakes or by reducing the slip rate that is converted into seismic energy. WG-07 decided to follow the practice of past Working Groups and the National Seismic Hazard Map and used creep rate (where it was judged to be interseismic, see Table P1) to reduce the area of the fault surface that generates seismic events. In addition to following past practice, this decision allowed the Working Group to use a reduction of slip rate as a separate factor to accommodate aftershocks, post seismic slip, possible aseismic permanent deformation along fault zones and other processes that are inferred to affect the entire surface area of a fault, and thus are better modeled as a reduction in slip rate. C-zones are also handled by a reduction in slip rate, because they are inferred to include regions of widely distributed shear that is not completely expressed as earthquakes large enough to model. Because the ratio of the rate of creep relative to the total slip rate is often used to infer the average depth of creep, the depth of creep can be calculated and used to reduce the surface area of a fault that generates earthquakes in our model. This reduction of surface area of rupture is described by an aseismicity factor, assigned to each creeping fault in Appendix A. An aseismicity factor of less than 1 is only assigned to faults that are inferred to creep during the entire interseismic period. A single aseismicity factor was chosen for each section of the fault that creeps by expert opinion from the observations documented here. Uncertainties were not determined for the aseismicity factor, and thus it represents an unmodeled (and difficult to model) source of error. This Appendix simply provides the documentation of known creep, the type and precision of its measurement, and attempts to characterize the creep as interseismic, afterslip, transient or triggered. Parts 2 and 3 of this Appendix compare the WG-07 deformation model and the seismic source model it generates to the strain generated by the Pacific - North American plate motion. The concept is that plate motion generates essentially all of the elastic strain in the vicinity of the plate boundary that can be released as earthquakes. Adding up the slip rates on faults and all others sources of deformation (such as C-zones and distributed background seismicity) should approximately yield the plate motion. This addition is usually accomplished by one of four approaches: 1) line integrals that sum deformation along discrete paths through the deforming zone between the two plates, 2) seismic moment tensors that add up seismic moment of a representative set of earthquakes generated by a crustal volume spanning the plate boundary, 3) strain tensors generated by adding up the strain associated with all of the faults in a crustal volume spanning the plate

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Summary and Analysis of the U.S. Government Bat Banding Program

This report summarizes the U.S. Government Bat Banding Program (BBP) from 1932 to 1972. More than 2 million bands were issued during the program, of which approximately 1.5 million bands were applied to 36 bat species by scientists in many locations in North America including the U.S., Canada, Mexico, and Central America. Throughout the BBP, banders noticed numerous and deleterious effects on bats, leading to a moratorium on bat banding by the U.S. Fish and Wildlife Service, and a resolution to cease banding by the American Society of Mammalogists in 1973. One of the main points of the memorandum written to justify the moratorium was to conduct a 'detailed evaluation of the files of the bat-banding program.' However, a critical and detailed evaluation of the BBP was never completed. In an effort to satisfy this need, I compiled a detailed history of the BBP by examining the files and conducting a literature review on bat banding activities during the program. I also provided a case study in managing data and applying current mark-recapture theory to estimate survival using the information from a series of bat bands issued to Clyde M. Senger during the BBP. The majority of bands applied by Senger were to Townsend's big-eared bat (Corynorhinus townsendii), a species of special concern for many states within its geographic range. I developed a database management system for the bat banding records and then analyzed and modeled survival of hibernating Townsend's big-eared bats at three main locations in Washington State using Cormack-Jolly-Seber (CJS) open models and the modeling capabilities of Program MARK. This analysis of a select dataset in the BBP files provided relatively precise estimates of survival for wintering Townsend's big-eared bats. However, this dataset is unique due to its well-maintained and complete state and because there were high recapture rates over the course of banding; it is doubtful that other unpublished datasets of the same quality exist buried in the BBP files for further analyses. Lastly, I make several recommendations based on the findings of this summary and analysis, the most important of which is that marking bats with standard metal or split-ring forearm bands should not be considered for mark-recapture studies unless the information sought and the potential for obtaining unbiased estimates from that information vastly outweighs the potential negative effects to the bats.

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Seismicity of the Earth 1900-2007, Kuril-Kamchatka arc and vicinity

This map shows details of the Kuril-Kamchatka arc not visible in an earlier publication, U.S. Geological Survey Scientific Investigations Map 3064. The arc extends about 2,100 km from Hokkaido, Japan, along the Kuril Islands and the pacific coast of the Kamchatka, Russia, peninsula to its intersection with the Aleutian arc near the Commander Islands, Russia. It marks the region where the Pacific plate subducts into the mantle beneath the Okhotsk microplate, a part of the larger North America plate. This subduction is responsible for the generation of the Kuril Islands chain and the deep offshore Kuril-Kamchatka trench. Relative to a fixed North America plate, the Pacific plate is moving northwest at a rate that decreases from 83 mm per year at the arc's southern end to 75 mm per year near its northern edge.

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Seismicity of the Earth 1900-2007, Japan and vicinity

This map shows details of Japan and vicinity not visible in an earlier publication, U.S. Geological Survey Scientific Investigations Map 3064. Japan and its island possessions lie across four major tectonic plates: Pacific plate, North America plate; Eurasia plate; and Philippine Sea plate. The Pacific plate is subducted into the mantle, beneath Hokkaido and northern Honshu, along the eastern margin of the Okhotsk microplate, a proposed subdivision of the North America plate (Bird, 2003). Farther south, the pacific plate is subducted beneath volcanic islands along the eastern margin of the Philippine Sea plate. This 2,200 km-long zone of subduction of the Pacific plate is responsible for the creation of the deep offshore Ogasawara and Japan trenches as well as parallel chains of islands and volcanoes, typical of the Circumpacific island arcs. Similarly, the Philippine Sea plate is itself subducting under the Eurasia plate along a zone, extending from Taiwan to southern Honshu, that comprises the Ryuku Islands and the Nansei-Shonto trench.

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Seismicity of the Earth 1900-2010 Mexico and vicinity

Mexico, located in one of the world's most seismically active regions, lies on three large tectonic plates: the North American plate, Pacific plate, and Cocos plate. The relative motion of these tectonic plates causes frequent earthquakes and active volcanism and mountain building. Mexico's most seismically active region is in southern Mexico where the Cocos plate is subducting northwestward beneath Mexico creating the deep Middle America trench. The Gulf of California, which extends from approximately the northern terminus of the Middle America trench to the U.S.-Mexico border, overlies the plate boundary between the Pacific and North American plates where the Pacific plate is moving northwestward relative to the North American plate. This region of transform faulting is the southern extension of the well-known San Andreas Fault system.

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Grassland birds wintering at U.S. Navy facilities in southern Texas

Grassland birds have undergone widespread decline throughout North America during the past several decades. Causes of this decline include habitat loss and fragmentation because of conversion of grasslands to cropland, afforestation in the East, brush and shrub invasion in the Southwest and western United States, and planting of exotic grass species to enhance forage production. A large number of exotic plant species, including grasses, have been introduced in North America, but most research on the effects of these invasions on birds has been limited to breeding birds, primarily those in northern latitudes. Research on the effects of exotic grasses on birds in winter has been extremely limited. This is the first study in southern Texas to examine and compare winter bird responses to native and exotic grasslands. This study was conducted during a period of six years (2003–2009) on United States Navy facilities in southern Texas including Naval Air Station–Corpus Christi, Naval Air Station–Kingsville, Naval Auxiliary Landing Field Waldron, Naval Auxiliary Landing Field Orange Grove, and Escondido Ranch, all of which contained examples of native grasslands, exotic grasslands, or both. Data from native and exotic grasslands were collected and compared for bird abundance and diversity; ground cover, vegetation density, and floristic diversity; bird and vegetation relationships; diversity of insects and arachnids; and seed abundance and diversity. Effects of management treatments in exotic grasslands were evaluated by comparing numbers and diversity of birds and small mammals in mowed, burned, and control areas. To determine bird abundance and bird species richness, birds were surveyed monthly (December–February) during the winters of 2003–2008 in transects (100 meter × 20 meter) located in native and exotic grasslands distributed at all five U.S. Navy facilities. To compare vegetation in native and exotic grasslands, vegetation characteristics were measured during 2003–2008 in the same transects used for bird surveys and included five measures of ground cover, plus estimates of plant species richness, vegetation density (visual obstruction) at two different heights, and shrub numbers. These data, plus seasonal rainfall, were then used to evaluate components of variation in native and exotic grasslands. Relations between total bird numbers and bird species richness with environmental variation in native and exotic grasslands were compared. To compare diversity of arthropods in native and exotic grasslands, insects and arachnids were collected using three different methodologies (standardized sweep-net, random sweep-net, and pitfall traps) during four seasons, (2005–2006), at Naval Air Station–Corpus Christi, Naval Auxiliary Landing Field Waldron, and Naval Air Station–Kingsville. To compare seed abundance and diversity between native and exotic grasslands, seeds were collected for two winters (2004–2006) at Naval Air Station–Corpus Christi and Naval Air Station–Kingsville. To evaluate effects of management on grassland vertebrates, abundance and diversity of birds and small mammals were estimated and compared in exotic grasses subjected to mowing, burning, or no active management (control) for one full year (2008–2009). Observations were made of 1,044 birds of 30 species in grassland transects during five winters. The Savannah Sparrow ( Passerculus sandwichensis ) was the most common bird, which, with 644 detections, accounted for 63 percent of all individuals identified to species. Meadowlarks ( Sturnella spp. ) and Le Conte’s Sparrows ( Ammodramus leconteii ) were the second (10 percent) and third (7 percent) most abundant bird species, respectively. Six of the seven most abundant species detected in grasslands were grassland species, and their numbers accounted for 87 percent of all birds, but 20 of the 30 species (67 percent) that used grasslands were not grassland species. Seven species observed in grassland transects during the study were Species of Conservation Concern: Le Conte’s Sparrow, Sedge Wren ( Cistothorus platensis ), Grasshopper Sparrow ( Ammodramus savannarum ), Long-billed Curlew ( Numenius americanus ), Sprague’s Pipit ( Anthus spragueii ), Cassin’s Sparrow ( Aimophila cassinii ), and Loggerhead Shrike ( Lanius ludovicianus ). Native grasslands consistently supported greater bird species richness than exotic grasslands. In one winter, exotic grasslands supported more birds than native grasslands. Native grasslands were determined to have more forb cover, more bare ground, and greater plant species richness than exotic grasslands, whereas exotic grasslands were characterized by more grass cover and relatively greater vegetation density during dry years. Not only did these individual measures differ between native and exotic grasslands, but components of variation also differed. In native grasslands, grass density and cover contributed more to variation, whereas in exotic grasslands, non-grass vegetation was a greater component of variation. Total bird numbers and bird species richness in native grasslands were related to the principal component that contained a measure of litter cover. Total bird numbers and bird species richness in exotic grasslands indicated no significant relationships with any of the principal components of variation. The two most common insect orders in native grasslands were Hymenoptera and Coleoptera, which accounted for 42 percent of all insects. The two most common insect orders in exotic grasslands were Hemiptera and Homoptera, which accounted for about 80 percent of all insects. Insect family richness was greater in exotic grasslands than in native grasslands in two of four seasons. Proportions of arachnid families were similar in native and exotic grasslands, but arachnid family richness was greater in exotic grasslands than in native grasslands. Abundance of seeds was greater in exotic than in native grasslands. However, seed diversity was greater in native grasslands than in exotic grasslands. Among the three types of management (mowed, burned, and control) applied to exotic grasses, birds were most abundant in the mowed area. Sedge Wrens, however, were never encountered in mowed sites. Meadowlarks were similarly abundant in all treatments, but Le Conte’s Sparrows were detected only in the control (unmanaged) area. Hispid cotton rats ( Sigmodon hispidus ) accounted for 93 percent of all rodent captures, with the number of captures peaking December through February. Hispid cotton rat numbers and total rodent numbers were greatest in control and pre-burn areas, and lowest in the mowed area. Mammal diversity, however, was greatest in the mowed habitat. Native and exotic grasslands differed essentially in all categories (bird numbers and diversity, vegetation characteristics, components of variation, diversity of insects and arachnids, and seed abundance and diversity) used to measure and compare them. This indicates that fundamental ecosystem processes have been altered after native grasslands have undergone invasion and ultimate domination by exotic grass species. Future research in Texas grassland ecosystems is essential because: 1) Texas sustains more area in grasslands than any other state or province in the Central Flyway; 2) Texas serves as the winter destination or migration pathway for hundreds of species of birds, including winter residents and Neotropical migrants; 3) ecology, distribution, and numbers of grassland birds wintering in southern latitudes of the United States remains poorly understood; and 4) climate change threatens to further accelerate advances of invading grass species.

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Removal of nonnative slider turtles (Trachemys scripta) and effects on native Sonora mud turtles (Kinosternon sonoriense) at Montezuma Well, Yavapai County, Arizona

The National Park Service (NPS) estimates that 234 national parks contain nonnative, invasive animal species that are of management concern (National Park Service, 2004). Understanding and controlling invasive species is thus an important priority within the NPS (National Park Service, 1996). The slider turtle (Trachemys scripta) is one such invasive species. Native to the Southeastern United States (Ernst and Lovich, 2009), as well as Mexico, Central America, and portions of South America (Ernst and Barbour, 1989), the slider turtle has become established throughout the continental United States and in other locations around the world (Burke and others, 2000). Slider turtle introductions have been suspected to be a threat to native turtles (Holland 1994; da Silva and Blasco, 1995), however, there has not been serious study of their effects until recently. Cadi and Joly (2003) found that slider turtles outcompeted European pond turtles (Emys orbicularis) for preferred basking sites under controlled experimental conditions, demonstrating for the first time direct competition for resources between a native and an exotic turtle species. Similarly, Spinks and others (2003) suggested that competition for basking sites between slider turtles and Pacific pond turtles (Actinemys marmorata) was partly responsible for the decline of Pacific pond turtles observed at their study site in California. They concluded that the impact of introduced slider turtles was 'almost certainly negative' for the western pond turtle. In the most recent critical study to assess the effects of introduced slider turtles on native turtles, Cadi and Joly (2004) demonstrated that European pond turtles that were kept under experimentally controlled conditions with slider turtles lost body weight and exhibited higher rates of mortality than in control groups of turtles comprised of the same species, demonstrating potential population-level effects on native species. Slider turtles are not native to Arizona but have been introduced in several areas in the southern and central part of the State, including Montezuma Well (the Well). The only native turtle at the Well is the Sonora mud turtle (Kinosternon sonoriense). Interactions between sliders and mud turtles have not been investigated at the Well or elsewhere. However, basking sites preferred by aquatic turtles are rare at the Well, suggesting one potential avenue for resource competition between sliders and Sonora mud turtles. In this study, we collected data on both species to evaluate the possible effects of slider turtles on Sonora mud turtles at Montezuma Well. During live trapping in the spring, summer, and early fall of 2007 and 2008, we removed slider turtles that we captured in the Well. We also collected ecological data on the mud turtles captured in the trapping effort. Separate behavioral observations of the turtles in the Well provided additional information on the ecology of the two species in the unusual environment of the Well, and also of interactions between the sliders and mud turtles. In this report, we describe the results of 2 yr of study of the turtles of Montezuma Well. We incorporate older data on the mud turtles in the Well to assess long-term population trends and potential response to the introduced slider turtles. We also report on aspects of basic ecology for the poorly understood Sonora mud turtle. The National Park Service requested that we incorporate public outreach as part of this research effort, so we also describe the outreach efforts associated with the turtle study.

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The potential influence of changing climate on the persistence of salmonids of the inland west

The Earth's climate warmed steadily during the 20th century, and mean annual air temperatures are estimated to have increased by 0.6°C (Intergovernmental Panel on Climate Change, 2007). Although many cycles of warming and cooling have occurred in the past, the most recent warming period is unique in its rate and magnitude of change (Siegenthaler and others, 2005) and in its association with anthropogenic emissions of greenhouse gases (Intergovernmental Panel on Climate Change , 2007). The climate in the western United States warmed in concert with the global trend but at an accelerated rate (+0.8°C during the 20th century; Saunders and others, 2008). The region could also prove especially sensitive to future changes because the relatively small human population is growing rapidly, as are demands on limited water supplies. Regional hydrological patterns are dominated by seasonal snow accumulation at upper elevations. Most of the region is relatively dry, and both terrestrial and aquatic ecosystems are strongly constrained b y water availability (Barnett and others, 2008; Brown and others, 2008). Stream environments are dynamic and climatically extreme, and salmonid fishes are the dominant elements of the native biodiversity (McPhail and Lindsey, 1986; Waples and others, 2008). Salmonids have broad economic and ecologic importance, but a century of intensive water resource development, nonnative fish stocking, and land use has significantly reduced many populations and several taxa are now protected under the Endangered Species Act (Thurow and others, 1997; Trotter, 2008). Because salmonids require relatively pristine, cold water environments and are often isolated in headwater habitats, members of this group may be especially vulnerable to the effects of a warming climate (Keleher and Rahel, 1996; Rieman and others, 2007; Williams and others, 2009). Warming during the 20th century drove a series of environmental trends that have profound implications for many aspects of salmonid habitat, including disturbance regimes such as wildfire, and unfavorable changes to thermal and hydrologic properties of aquatic systems. Warmer air temperatures have been associated with decreased winter snow accumulations, have accelerated snowmelt, and have advanced the timing of peak runoff by several days to weeks across most of western North America (Stewart and others, 2005; Barnett and others, 2008). Less snow and earlier runoff decrease aquifer recharge, make less water available for groundwater inputs to streams, and are contributing to widespread decreases in summer low flows (Stewart and others, 2005; Rood and others, 2008; Luce and Holden 2009). Interannual variability in stream flow is increasing, as is the persistence of multi-year extreme conditions (McCabe and others, 2004; Pagano and Garen 2005). In many areas of western North America, flood risks have increased in association with warmer temperatures during the 20th century (Hamlet and Lettenmaier, 2005). Streams where midwinter temperatures are near freezing have proven especially sensitive to increased flooding because of associated transitional hydrological patterns (mixtures of rainfall and snowmelt) and propensity for occasional rain-on-snow events to rapidly melt winter snowpack and generate large floods (Hamlet and Lettenmaier, 2005). Stream temperatures in many areas are increasing (Peterson and Kitchell, 2001; Morrison and others, 2002; Bartholow, 2005; Kaushal and others, 2010), due to both air temperature increases and reduced summer flows that make streams more sensitive to warmer air temperatures (Isaak and others, 2010). In recent decades, wildfires have become more common across much of the western United States during periods of more frequent droughts (Westerling and others, 2006; Hoerling and Eischeid, 2007), and local stream temperature can increase in postfire environments (Gresswell, 1999; Dunham and others, 2007). Fire-related temperature increase within streams is commonly a transient phenomenon, lasting only until riparian vegetation has recovered (Gresswell, 1999); however, ongoing climate change could preclude recovery to higher stature, prefire vegetation types in some areas (McKenzie and others, 2004; van Mantgem and Stephenson, 2007), resulting in a loss of critical riparian shading. Additionally, when wildfires occur in steep mountain topographies, the vegetation that stabilize s soils on hillslopes is often killed and landslides become more prevalent (Gresswell, 1999). Landslides int o stream channels form debris flows composed of sediment slurries and dead trees that can scour channels to bedrock and further exacerbate stream heating, delay recovery of riparian areas, or extirpate fish populations (Gresswell, 1999; May and Gresswell, 2003; Dunham and others, 2007). Changes in stream environments will shift habitat distributions, sometimes unpredictably, in both time and space for many salmonid fishes. Water temperature fundamentally influences aquatic ecosystem health because distribution, reproduction, fitness, and survival of ectothermic organisms are inextricably linked to the thermal regime of the environment. Historically, research has focused on defining lethal thermal limits of salmonids (Eaton and others, 1995; Selong and others, 2001; Todd and others, 2008); however, water temperature is known to be important in biological processes at a variety of spatial scales and levels of biological organization (Rahel and Olden, 2008; McCullough and others, 2009). For instance, trout are affected directly by water temperature through feeding, metabolism, and growth rates, and indirectly by factors such as prey availability and species interactions (Wehrly and others, 2007; Rahel and Olden, 2008). Where cold water temperatures currently limit habitat suitability and distributions of some species (for example, at the highest and most northerly distributional extents; Nakano and others, 1996; Coleman and Fausch, 2007), a warming climate may gradually increase the quality and extent of suitable habitat. Over time, previously constrained populations are expected to expand into these new habitats and increase in number. Some evidence suggests this may already be happening in Alaska, where streams in recently deglaciated areas are being colonized by emigrants from nearby salmon and char populations (Milner and others, 2000). Unfortunately, many of the sensitive salmonid species that are often the focus of western managers are unlikely to benefit from future water temperature increases. Warmer stream temperatures will facilitate invasion by nonnative species that are broadly established in downstream areas into upstream areas where they will compete with native species (Rieman and others, 2006; Rahel and Olden, 2008; Fausch and others, 2009). In other cases, warmer stream temperatures will render thermally suitable habitats unsuitable in downstream areas and effect net losses of habitat because upstream distributions are often constrained by streams that are too small or steep (Hari and others, 2006; Isaak and others, 2010). Both scenarios are realistic for fish species like bull trout ( Salvelinus confluentus ) (Rieman and others, 2006; Rieman and others, 2007), the various subspecies of cutthroat trout ( Oncorhynchus clarkii ) (Williams and others, 2009), Gila trout ( Oncorhynchus gilae gilae ) (Kennedy and others, 2008), and Apache trout ( Oncorhynchus gilae apache ) (Rinne and Minckley, 1985; Carmichael and others, 1993). As native species are increasingly confined to smaller and more isolated habitats by a gradually warming climate, the effects of wildfires (whether related to lethal changes in water quality during a fire, channel debris flows, or chronic postfire warming ) could have greater proportional effects on remaining habitats (for example, Brown and others, 2001; Rieman and others, 2007). If these changes were accompanied by additional hydrologic alterations associated with changes to the magnitude, frequency, duration, timing, and rate of change of discharge patterns (Jager and others, 1999; Henderson and others, 2000), populations may begin to lose some of their historic resilience and become ever more susceptible to local extirpations. As dramatic and extensive as climatic and environmental trends are for salmonid habitats, global climate models (GCMs) project that many of these trends will continue and even accelerate until at least the middle of the 21st century (Intergovernmental Panel on Climate Change, 2007). Current projections suggest mean annual air temperatures will increase by an additional 1–3°C, and early indications are that climate trajectory is at the higher end of this range (Pittock, 2006; Raupach and others, 2007). Although predicted changes vary considerably, even the most conservative estimates suggest a warming rate that will be twice that observed during the 20th century. Projections for the midcentury are most certainly due to the effects of greenhouse gases already emitted or predicted in the short term, uncertainties of the effects of longer-term greenhouse gas emissions, short-term climate cycles, and process errors associated with climate models (Cox and Stephenson, 2007). Projections of changes in total precipitation are less certain than those for air temperatures, but most GCMs project relatively small changes in the Northwest, with the exception of slightly drier summer periods (Mote and others, 2008; Karl and others, 2009). In the Southwest, however, significant decreases (such as 15–30 percent ) are projected during most periods of the year, and this area is one of the few for which Intergovernmental Panel on Climate Change (2007) precipitation projections have a high level of certainty (Hoerling and Eischeid, 2007; Karl and others, 2009). Clearly, managers of native salmonids in the wester n United States should consider adjusting management strategies to accommodate a warmer and possibly drier future (Williams and others, 2009). Tools are needed to forecast where important changes may occur and how conservation efforts should be prioritized. In this Open-File Report, we document our initial efforts in this regard for 10 species and subspecies of inland trout and Montana Arctic grayling ( Thymallus arcticus ) across the western United States.

Arizona, California, Colorado, Idaho, Montana, Nev↗

Accounts of damage from historical earthquakes in the northeastern Caribbean to aid in the determination of their location and intensity magnitudes

Earthquakes have been documented in the northeastern Caribbean since the arrival of Columbus to the Americas; written accounts of these felt earthquakes exist in various parts of the world. To better understand the earthquake cycle in the Caribbean, the records of earthquakes in earlier catalogs and historical documents from various archives, which are now available online, were critically examined. This report updates previous catalogs of earthquakes, in particular earthquakes in Hispaniola, to give to the public the most comprehensive documentation of earthquake damage and to further the understanding of the earthquake cycle in the northeastern Caribbean. Documentation of an event in the past depended on the population and political trends of the island, and the availability of historical documents is limited by the physical resource digitization schedule and by the copyright laws of each archive. Examples of documents accessed are governors' letters, newspapers, and other circulars published within the Caribbean, North America, and Western Europe. Key words were used to search for publications that contain eyewitness accounts of various large earthquakes. Finally, this catalog provides descriptions of damage to buildings used in previous studies for the estimation of moment intensity (MI) and location of significantly damaging or felt earthquakes in Hispaniola and in the northeastern Caribbean, all of which have been described in other studies.

Open-File Report↗

Fission products in National Atmospheric Deposition Program&mdash;Wet deposition samples prior to and following the Fukushima Dai-Ichi Nuclear Power Plant incident, March 8?April 5, 2011

Radioactive isotopes I-131, Cs-134, or Cs-137, products of uranium fission, were measured at approximately 20 percent of 167 sampled National Atmospheric Deposition Program monitoring sites in North America (primarily in the contiguous United States and Alaska) after the Fukushima Dai-Ichi Nuclear Power Plant incident on March 12, 2011. Samples from the National Atmospheric Deposition Program were analyzed for the period of March 8-April 5, 2011. Calculated 1- or 2-week radionuclide deposition fluxes at 35 sites from Alaska to Vermont ranged from 0.47 to 5,100 Becquerels per square meter during the sampling period of March 15-April 5, 2011. No fission-product isotopes were measured in National Atmospheric Deposition Program samples obtained during March 8-15, 2011, prior to the arrival of contaminated air in North America.

Puerto Rico;U.S. Virgin Islands;North America↗

A bibliography of literature pertaining to plague ( Yersinia pestis )

Plague is an acute and often fatal zoonotic disease caused by the bacterium Yersinia pestis . Y. pestis mainly cycles between small mammals and their fleas; however, it has the potential to infect humans and frequently causes fatalities if left untreated. It is often considered a disease of the past; however, since the late 1800s, plagueis geographic range has expanded greatly, posing new threats in previously unaffected regions of the world, including the Western United States. A literature search was conducted using Internet resources and databases. The keywords chosen for the searches included plague, Yersinia pestis , management, control, wildlife, prairie dogs, fleas, North America, and mammals. Keywords were used alone or in combination with the other terms. Although this search pertains mostly to North America, citations were included from the international research community, as well. Databases and search engines used included Google ( http://www.google.com ), Google Scholar ( http://scholar.google.com ), SciVerse Scopus ( http://www.scopus.com ), ISI Web of Knowledge ( http://apps.isiknowledge.com ), and the USGS Library's Digital Desktop ( http://library.usgs.gov ). The literature-cited sections of manuscripts obtained from keyword searches were cross-referenced to identify additional citations or gray literature that was missed by the Internet search engines. This Open-File Report, published as an Internet-accessible bibliography, is intended to be periodically updated with new citations or older references that may have been missed during this compilation. Hence, the authors would be grateful to receive notice of any new or old papers that the audience (users) think need to be included.

Open-File Report↗

Digital geologic map of the Redding 1° x 2° quadrangle, Shasta, Tehama, Humboldt, and Trinity Counties, California

The Redding 1° x 2° quadrangle in northwestern California transects the Franciscan Complex and southern Klamath Mountains province as well as parts of the Great Valley Complex, northern Great Valley, and southernmost Cascades volcanic province. The tectonostratigraphic terranes of the Klamath province represent slices of oceanic crust, island arcs, and overlying sediment that range largely from Paleozoic to Jurassic in age. The Eastern Klamath terrane forms the nucleus to which the other terranes were added westward, primarily during Jurassic time, and that package was probably accreted to North America during earliest Cretaceous time. The younger Franciscan Complex consists of a sequence of westward younging tectonostratigraphic terranes of late Jurassic to Miocene age that were accreted to North America from mid-Cretaceous through Miocene time, with the easternmost being the most strongly metamorphosed. The marine Great Valley sequence, of late Jurassic and Cretaceous age, was deposited unconformably across the southernmost Klamath rocks, but in turn was underthrust at its western margin by Eastern belt Franciscan rocks. Pliocene and Quaternary volcanic rocks and sediment of the Cascades province extend into the southeastern part of the quadrangle, abutting the northernmost part of the great central valley of California. This map and database represent a digital rendition of Open-File Report 87-257, 1987, by L.A. Fraticelli, J.P. Albers, W.P. Irwin, and M.C. Blake, Jr., with various improvements and additions.

California↗

Fire history of Everglades National Park and Big Cypress National Preserve, southern Florida

Fire occurs naturally in the environment on most continents, including Africa (Ryan and Williams, 2011), Asia (Kauhanen, 2008), Australia (Kutt and Woinarski, 2007), Europe (Eshel and others, 2000), South America (Fidelis and others, 2010), and North America (Van Auken, 2000). Antarctica appears to be the only continent that has no reported natural fires, although fire is common in grasslands of Patagonia and on islands in the Subantarctic region (Gonzalez and others, 2005; McGlone and others, 2007). Natural fires also have occurred over thousands of years, and the frequencies of these natural fires have changed (Power and others, 2008). This has resulted in altered ecosystems at landscape scales. Recent evidence suggests that the treeless desert pastures of Tibet once were forests and woodlands, and charcoal deposits indicate that fire was more frequent in the past (Miehe and others, 2006). Human cultural development has been influenced by changes in natural fire frequencies. Zong and others (2007) reported that human suppression of fires in coastal areas of China allowed the development of rice paddy cultivation and, thus, increased the size of human populations. In addition to its almost world-wide occurrence, fire plays a role in a wide variety of ecosystem types. Grassland, savanna, steppe, woodland, forest, and wetland ecosystems all have fire as part of their natural ecology (Veblen and Lorenz, 1988; Chokkalingam and others, 2007; Miller and others, 2009, Keith and others, 2010; Staver and others, 2011). Fires affect these ecosystems in various ways, the most obvious of which is the direct effect on plant biomass (for example, Van Wilgen, 1982; Mack and others, 2008). However, fire has many other effects on ecosystems. Plant species richness, diversity, and functional types can change in response to fire (Peterson and Reich, 2008). All properties of the surface soils (such as bulk density, particle size distribution, pH, and organic carbon and nitrogen content) can be altered by the frequency and severity of fire (Boerner and others, 2009). Faunal communities will respond to fire, with some species increasing (Fuhlendorf and others, 2006) and other species decreasing, after the fire (Vasconcelos and others, 2009).The position of the ecotone between differing ecosystems also is influenced by fire occurrence (Heisler and others, 2003; Briggs and others, 2005; Smith and others, 2013). Fire has been used as a management tool in various ecosystems around the world. Prairies, grasslands, and savannas are fire-maintained ecosystems where fire is used to deter invasion by shrubs and trees (Grant and others, 2009; Scheintaub and others, 2009). Similarly, fire plays an important role in woodlands and forests by influencing species composition and succession such, as the use of fire in coniferous forests to prevent encroachment by hardwoods (Phillippe and others, 2011). Fire also has been used to manage wetland ecosystems for more than 50 years (Lynch, 1941; Frost, 1995). Uses have included returning marshes to early successional states, increasing forage for wildlife (Lynch, 1941). In all fire-influenced ecosystems, prescribed burns are routinely used to reduce fuel loads, reducing the possibility of catastrophic fires.

Florida↗

Sixth International Limnogeology Congress: abstract volume, Reno, Nevada, June 15-19, 2015

Limnogeology is the study of modern lakes and lake deposits in the geologic record. Limnogeologists have been active since the 1800s, but interest in limnogeology became prevalent in the early 1990s when it became clear that lake deposits contain continental environmental and climate records. A society that is focused on limnogeology would allow greater communication and access to research on these important subjects and contribute to providing sound science used to understand rapid global changes in our modern world; thus, the International Association of Limnogeology was founded in 1995 at the first International Limnogeology Congress (ILIC) held in Copenhagen, Denmark. The Sixth International Limnogeology Congress (ILIC6) was held in Reno, Nevada, from June 15&ndash;19, 2015. The ILIC meetings have been held every 4 years since the first meeting in1995 and were subsequently convened in Brest, France (1999), Tucson, Arizona, USA (2003), Barcelona, Spain (2007), and Konstanz, Germany (2011). The Congress in Reno, USA marks the second time the Congress has been held in the United States and more than 150 scientists from every part of the world participated. About one-half of the participants were from North America, together with scientists from Europe, South America, Asia, Africa, Australia, and New Zealand. The format of the Reno Congress followed the format originated at the Tucson Congress (ILIC3), which is unusual for scientific meetings. Nine keynote speakers spread throughout the Congress gave 1-hour talks, with the rest of the time available for viewing posters that were presented by the bulk of the participants. Keynote presentations were diverse and showed the breadth of research that is being done in lake systems worldwide. The abstracts of the keynote speakers and about 140 poster presentations are included in this volume. These posters cover a variety of limnologic, paleolimnologic, and limnogeologic topics including contaminant histories of lakes, the role of groundwater in lake processes, the formation of minerals in lake sediments, terminal lakes, how lakes reveal climate changes and paleohydrologic processes, the impact of volcanic emissions on lakes, as well as the biologic and chemical evolution of lake systems. The U.S. Geological Survey has sponsored each ILIC that has been held in the United States because of the importance of understanding paleoclimate and contaminant histories of lakes, two main themes of the Congress. This volume provides a permanent record of the wide variety of studies that are being conducted in modern lakes and ancient lake deposits worldwide, and it provides a stepping stone for any one desiring further discussion of the work that was presented at ILIC6.

Open-File Report↗