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At least 1,153 records · Page 64Linked to original sources

Recovery of prairie fish assemblages at the transition from channelized to nonchannelized: Implications for conservation of natural channels

Fish assemblages were systematically sampled along the transition from channelized to unchannelized reaches in seven streams in northern Missouri, USA. Streams ranged in size from 4th to 8th order and were located in the Central Dissected Till Plains including the Grand, Chariton, Salt, and Fabius watersheds. Maximum species richness was reached 3-5 km downstream from the end of channelization. A limited core group of 10 species was present at most of the sites (channelized and unchannelized locations), and a diverse group of 45 species was present at relatively few sites (rarely channelized locations). The core group consisted largely of tolerant, omnivorous species and contained no top carnivores. The 45-species diverse group included a greater proportion of intolerant, benthic invertivorous, lithophilous, and carnivorous species. The effect of channelization extended well into unchannelized reaches and should be considered by conservation planners.

Missouri↗

A natural resource condition assessment for Sequoia and Kings Canyon National Parks: Appendix 22: climatic change

Climate is a master controller of the structure, composition, and function of biotic communities, affecting them both directly, through physiological effects, and indirectly, by mediating biotic interactions and by influencing disturbance regimes. Sequoia and Kings Canyon National Park’s (SEKI’s) dramatic elevational changes in biotic communities -- from warm mediterranean to cold alpine -- are but one manifestation of climate’s overarching importance in shaping SEKI’s landscape. Yet humans are now altering the global climate, with measurable effects on ecosystems (IPCC 2007). Over the last few decades across the western United States, human-induced climatic changes have likely contributed to observed declines in fraction of precipitation falling as snow and snowpack water content (Mote et al. 2005, Knowles et al. 2006), advance in spring snowmelt (Stewart et al. 2005, Barnett et al. 2008), and consequent increase in area burned in wildfires (Westerling et al. 2006). In the Sierra Nevada, warming temperatures have likely contributed to observed glacial recession (Basagic 2008), uphill migration of small mammals (Moritz et al. 2008), and increasing tree mortality rates (van Mantgem and Stephenson 2007, van Mantgem et al. 2009). More substantial changes can be expected for the future (e.g., IPCC 2007). Given the central importance of climate and climatic changes, we sought to describe long-term trends in temperature and precipitation at SEKI. Time and budget constraints limited us to analyses of mean annual temperature and mean annual precipitation, using readily-available data. If funds become available in the future, further analyses will be needed to analyze trends by season, trends in daily minimum and maximum temperatures, and so on. We chose to analyze data from individual weather stations rather than use interpolated climatic data from sources such as PRISM (http://www.prism.oregonstate.edu/). In topographically complex mountainous regions with few weather stations, like SEKI, the addition or subtraction of even a single weather station through time has the potential to significantly bias trends in interpolated data. In particular, this analysis was motivated by our questioning of some PRISM results presented in Appendix 1 (Landscape Context) that compared temperature averages between two 30-year periods of the 20th Century. Figures 6 and 11 of Appendix 1 indicate that recent (1971-2000) temperatures in northern Kings Canyon National Park averaged some 2° C cooler than those of 1911-1940. This would represent a truly profound and persistent cooling, and seems to be at odds both with the glacial retreats observed in the area over the century (Basagic 2008), and with the reported PRISM warming of nearly 2° C just to the west of the cooling (see Figs. 6 and 11 in Appendix 1). We suspect that the extreme localized Kings Canyon cooling reported by PRISM is an artifact of sparsely-distributed weather stations in the region being added and discontinued over the span of the 20th Century. For example, data from the Western Regional Climate Center (http://www.wrcc.dri.edu/coopmap/) suggest that for the period 1911 through 1924 PRISM must interpolate northern Kings Canyon temperatures based on a few low-elevation stations -- separated by hundreds of kilometers -- in Nevada and California’s San Joaquin Valley. In contrast, by 1970 PRISM interpolations will be dominated by closer, higher-elevation stations (see this report). The single weather station closest to northern Kings Canyon that has a temperature record at least partly spanning Appendix 1’s two 30-year time periods -- the Independence station, with a relatively continuous temperature record starting in 1925 -- shows a modest warming, not a cooling, between 1925-1940 and 1971-2000, further casting doubt on the Kings Canyon cooling shown in Figs. 6 and 11 of Appendix 1. If funds become available, it will be useful to more formally analyze potential PRISM biases in long-term SEKI climatic trends. Until then, the analyses of individual weather station records presented here (effectively an analysis of source data that PRISM uses) are meant to provide a robust summary of climatic changes in SEKI.

California↗

Natural and human-induced variability in barrier-island response to sea level rise

Storm-driven sediment fluxes onto and behind barrier islands help coastal barrier systems keep pace with sea level rise (SLR). Understanding what controls cross-shore sediment flux magnitudes is critical for making accurate forecasts of barrier response to increased SLR rates. Here, using an existing morphodynamic model for barrier island evolution, observations are used to constrain model parameters and explore potential variability in future barrier behavior. Using modeled drowning outcomes as a proxy for vulnerability to SLR, 0%, 28%, and 100% of the barrier is vulnerable to SLR rates of 4, 7, and 10 mm/yr, respectively. When only overwash fluxes are increased in the model, drowning vulnerability increases for the same rates of SLR, suggesting that future increases in storminess may increase island vulnerability particularly where sediment resources are limited. Developed sites are more vulnerable to SLR, indicating that anthropogenic changes to overwash fluxes and estuary depths could profoundly affect future barrier response to SLR.

New Jersey↗

Response to comment by Walker et al. on “From data to decisions: Processing information, biases, and beliefs for improved management of natural resources and environments”

Our different kinds of minds and types of thinking affect the ways we decide, take action, and cooperate (or not). The comment by Walker et al. (2018, https://doi.org/10.1002/2017EF000750 ) illustrates several points made by Glynn et al. (2017, https://doi.org/10.1002/2016EF000487 ) and many other articles. Namely, biases and beliefs often drive scientific reasoning, and scientists, just like other humans, are intimately attached to their values and heuristics. Scientists, just like many other people, also tend to read and interpret text in ways that best match their individual perceptions of a problem or issue: in many cases paraphrasing and changing the meaning of what they read to better match their initial ideas. Walker et al. are doing interesting and important research on uncertainty. Nonetheless, they misinterpret the work, assumptions, and conclusions brought forth by Glynn et al. (2017, https://doi.org/10.1002/2016EF000487 ).

Earth's Future↗

Empirical estimation of natural geoelectric hazards

Geoelectric field time series can be estimated by convolving estimates of Earth‐surface impedance, such as those obtained from magnetotelluric survey measurements, with historical records of geomagnetic variation obtained at magnetic observatories. This straightforward procedure permits the mapping of geoelectric field variation during magnetic storms. Statistical analysis of the time series allows extrapolation to extreme‐value amplitudes, such as might be realized during an intense magnetic storm in the future. The development of these products is illustrated for the Mid‐Atlantic United States, using impedances obtained from EarthScope survey data and geomagnetic variation records obtained at the Fredericksburg observatory operated by the U.S. Geological Survey. For this region, 100‐year geoelectric exceedance amplitudes have a range of almost three orders of magnitude (from 0.04 V/km at a site in southern Pennsylvania to 24.29 V/km at a site in central Virginia), and they have significant geographic granularity, which is due to site‐to‐site differences in surface impedance (and subsurface electrical conductivity structure). Maps of 100‐year exceedance amplitudes resemble those of geoelectric amplitudes for the March 1989 magnetic storm, and, in that sense, the March 1989 storm resembles what might be loosely called a “100‐year” event.

Book chapter↗

Value of information in natural resource management: technical developments and application to pink-footed geese

The “value of information” (VOI) is a generic term for the increase in value resulting from better information to guide management, or alternatively, the value foregone under uncertainty about the impacts of management (Yokota and Thompson, Medical Decision Making 2004; 24 : 287). The value of information can be characterized in terms of several metrics, including the expected value of perfect information and the expected value of partial information. We extend the technical framework for the value of information by further developing the relationship between value metrics for partial and perfect information and describing patterns of their performance. We use two different expressions for the expected value of partial information to highlight its relationship to the expected value of perfect information. We also develop the expected value of partial information for hierarchical uncertainties. We highlight patterns in the value of information for the Svalbard population of the pink-footed goose ( Anser brachyrhynchus ), a population that is subject to uncertainty in both reproduction and survival functions. The framework for valuing information is seen as having widespread potential in resource decision making, and serves as a motivation for resource monitoring, assessment, and collaboration.

Svalbard↗

Genetic implications of bottleneck effects of differing severities on genetic diversity in naturally recovering populations: An example from Hawaiian coot and Hawaiian gallinule

The evolutionary trajectory of populations through time is influenced by the interplay of forces (biological, evolutionary, and anthropogenic) acting on the standing genetic variation. We used microsatellite and mitochondrial loci to examine the influence of population declines, of varying severity, on genetic diversity within two Hawaiian endemic waterbirds, the Hawaiian coot and Hawaiian gallinule, by comparing historical (samples collected in the late 1800s and early 1900s) and modern (collected in 2012–2013) populations. Population declines simultaneously experienced by Hawaiian coots and Hawaiian gallinules differentially shaped the evolutionary trajectory of these two populations. Within Hawaiian coot, large reductions (between −38.4% and −51.4%) in mitochondrial diversity were observed, although minimal differences were observed in the distribution of allelic and haplotypic frequencies between sampled time periods. Conversely, for Hawaiian gallinule, allelic frequencies were strongly differentiated between time periods, signatures of a genetic bottleneck were detected, and biases in means of the effective population size were observed at microsatellite loci. The strength of the decline appears to have had a greater influence on genetic diversity within Hawaiian gallinule than Hawaiian coot, coincident with the reduction in census size. These species exhibit similar life history characteristics and generation times; therefore, we hypothesize that differences in behavior and colonization history are likely playing a large role in how allelic and haplotypic frequencies are being shaped through time. Furthermore, differences in patterns of genetic diversity within Hawaiian coot and Hawaiian gallinule highlight the influence of demographic and evolutionary processes in shaping how species respond genetically to ecological stressors.

Ecology and Evolution↗

Relative influence of flow regime, natural and anthropogenic environment on multidimensional stream fish diversity

The flow regime is considered a ‘master variable’ in riverine ecology because it directly influences stream geomorphology and biological communities. However, other environmental and anthropogenic factors have direct and synergistic effects with flow on fish diversity, complicating estimates of the flow regime's true importance. Moreover, most flow-ecology studies focus only on taxonomic diversity (i.e., species), without considering functional (trait-focused) or phylogenetic (evolution-focused) dimensions of diversity. In this study, we used linear regression with variation partitioning to parse out the independent and shared roles of the flow regime, physical environmental factors (e.g., soil characteristics) and the anthropogenic environment (e.g., developed land cover) for structuring multidimensional diversity of 365 stream fish communities in two biogeographic regions across South Carolina, USA. These variables explained between 8% and 18% of total variation of the local diversity. The flow regime contributed to diversity in all cases, but frequently covaried with physical and/or anthropogenic environmental variables. This covariation indicated that the independent role of flow would have been inflated if other environmental variables were not considered. The three dimensions of stream fish diversity were weakly correlated with one another and were associated with different environmental variables, indicating that each of them represents unique and complimentary facets of fish diversity. Accordingly, only considering the independent effects of instream flow on fish diversity may miss meaningful interactions between the flow regime and the other components of the environment that influence biodiversity patterns, leading to over simplified flow–ecology relationships.

South Carolina↗

Rapid determination of filterable residue in natural waters

The most widely used procedures for determining filterable residue (total dissolved solids) in water are macromethods given in Standard Methods. Although macromethods give good results, they require large amounts of water and long drying times. This report describes a microtechnique for determining filterable residue that requires only 0.05 ml of water and 15 min/sample drying time. The sensitivity of the method is within the range (4 mg/l or 5 per cent) given in Standard Methods and that reported by Sokoloff.

Journal - American Water Works Association↗