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At least 73 records · Page 4Linked to original sources
USGS2016

Collision and displacement vulnerability among marine birds of the California Current System associated with offshore wind energy infrastructure

With growing climate change concerns and energy constraints, there is an increasing need for renewable energy sources within the United States and globally. Looking forward, offshore wind-energy infrastructure (OWEI) has the potential to produce a significant proportion of the power needed to reach our Nation’s renewable energy goal. Offshore wind-energy sites can capitalize open areas within Federal waters that have persistent, high winds with large energy production potential. Although there are few locations in the California Current System (CCS) where it would be acceptable to build pile-mounted wind turbines in waters less than 50 m deep, the development of technology able to support deep-water OWEI (>200 m depth) could enable wind-energy production in the CCS. As with all human-use of the marine environment, understanding the potential impacts of wind-energy infrastructure on the marine ecosystem is an integral part of offshore wind-energy research and planning. Herein, we present a comprehensive database to quantify marine bird vulnerability to potential OWEI in the CCS (see https://doi.org/10.5066/F79C6VJ0 ). These data were used to quantify marine bird vulnerabilities at the population level. For 81 marine bird species present in the CCS, we created three vulnerability indices: Population Vulnerability, Collision Vulnerability, and Displacement Vulnerability. Population Vulnerability was used as a scaling factor to generate two comprehensive indicies: Population Collision Vulnerability (PCV) and Population Displacement Vulnerability (PDV). Within the CCS, pelicans, terns (Forster’s [ Sterna forsteri ], Caspian [ Hydroprogne caspia ], Elegant [ Thalasseus elegans ], and Least Tern [ Sternula antillarum ]), gulls (Western [ Larus occidentalis ] and Bonaparte’s Gull [ Chroicocephalus philadelphia ]), South Polar Skua ( Stercorarius maccormicki ), and Brandt’s Cormorant ( Phalacrocorax penicillatus ) had the greatest PCV scores. Brown Pelican ( Pelicanus occidentalis ) had the greatest overall PCV score. Some alcids (Scripps’s Murrelet [ Synthliboramphus scrippsi ], Marbled Murrelet [ Brachyramphus marmoratus ], and Tufted Puffin [ Fratercula cirrhata ]), terns (Elegant and Least Lern), and loons (Yellow-billed [ Gavia adamsii ] and Common Loon [ G. immer ]) had the greatest PDV scores. Ashy Storm-Petrel ( Oceanodroma homochroa ) had the greatest overall PDV score. To help inform decisions that will impact seabird conservation, vulnerability assessment results can now be combined with recent marine bird at-sea distribution and abundance data for the CCS to evaluate vulnerability areas where OWEI development is being considered. Lastly, it is important to note that as new information about seabird behavior and populations in the CCS becomes available, this database can be easily updated and modified.

Open-File Report↗
USGS2022

Potential effects of energy development on environmental resources of the Williston Basin in Montana, North Dakota, and South Dakota—Executive summary

Executive Summary The Williston Basin, which includes parts of Montana, North Dakota, and South Dakota in the United States and parts of Manitoba and Saskatchewan in Canada, has been explored as a potential source of energy resources since the early 20th century; however, commercially viable petroleum drilling and recovery began in earnest in the 1950s. When oil prices rose in the mid-1980s, the number of wells also increased and then subsequently declined. Interest in the Williston Basin increased again in the mid-2000s with the application of new drilling technology. Since then, development has increased rather quickly. Most of this new development has been facilitated by advances in horizontal drilling and hydraulic fracturing technologies. The North Dakota Department of Mineral Resources reported an increase of more than 10,000 producing wells between 2000 and the spring of 2016. In total, 84 percent of those 10,000 wells target the Bakken Formation, which is now home to one of the Nation’s largest energy booms. Current estimates suggest that exploration and drilling activities are expected to continue for the next 20 to 50 years; however, future activity will likely ebb and flow in response to energy prices. Although most energy has been developed on non-Federal property, more than 2,000 wells were started on federally managed lands in the three States that contain the Williston Basin between 2004 and 2015, though these numbers do not reflect whether or not these wells targeted the Bakken Formation. Executive Order no. 13604 (March 22, 2012) directs Federal agencies to improve the timeliness of the permitting process for extracting publically owned minerals, while minimizing negative environmental effects. This means that Federal agencies need information about how energy development may affect other resources they are tasked with managing. One example of where information about potential effects of development may be useful is the Bureau of Land Management’s permitting process. Permits may include stipulations or special conditions that limit unforeseen negative consequences or ameliorate potential conflicts of future development. Federal agencies also need to coordinate permitting actions to ensure that development complies with existing regulations (for example, the Endangered Species Act [16 U.S.C. § 1531 et seq.] or the National Environmental Protection Act [42 U.S.C. § 4321 et seq.]) without unnecessarily restricting or delaying development. Part of this coordination entails agreeing on the information that will be used to assess the potential effects of energy development, which should also improve efficiency of the permitting process. Within the Williston Basin, a group of Federal agencies called the Bakken Federal Executive Group is developing coordination strategies for numerous energy-related issues on Federal lands. This report was developed in cooperation with the Bureau of Land Management to provide them with the best available scientific information to support documentation of potential effects on resources that Federal agencies manage. This report summarizes information about the effects of energy development on air, water, and biological resources within the U.S. part of the Williston Basin. The topics discussed in the report were based on a prioritized list of information needs elicited from the Bakken Federal Executive Group. The list was developed using a process known as structured decision making or decision analysis. This process began with an initial scoping workshop to determine the range of decisions made by those involved directly in managing energy development and resources on public land. U.S. Geological Survey staff then developed a simple quantitative ranking tool to assess which information needs were of greatest importance to those decisions.

Montana, North Dakota, South Dakota↗
USGS2022

Counterfactuals to assess effects to species and systems from renewable energy development

Renewable energy production, mostly via wind, solar, and biofuels, is central to goals worldwide to reduce carbon emissions and mitigate anthropogenic climate change (IPCC, 2014; Pörtner et al., 2021). Nevertheless, adverse impacts to natural systems, especially fatalities of wildlife and alteration of habitat, are key challenges for renewable energy production (Allison et al., 2019; Katzner et al., 2019). Because of the magnitude of these challenges, extensive effort has been invested in surveys and science to understand the environmental effects of renewable energy on species and systems. Nevertheless, these impacts have not been formally compared relative to counterfactual conditions (Bull et al., 2021; Coetzee and Gaston, 2021), i.e., those occurring in the absence of renewable energy. As such, cumulative ecological impact assessments required by many regulating agencies typically only consider the adverse impacts of renewables, without evaluating whether mitigative effects of current and planned build-out (e.g., Larson et al., 2020) will offset their adverse impacts to species and natural systems (Allison et al., 2014). Accordingly, these critical decision processes have an insufficient perspective to foster fully informed decisions, and, for some species or systems, renewable energy could lead to more profound impacts than those it is intended to prevent. Furthermore, because of this approach and, despite the well-studied benefits to society of renewable energy development (IPCC, 2014), the ecological value of renewable energy is often premised on the plausible but untested assumption that its negative effects to natural populations and systems are less consequential than the negative effects in alternative scenarios with less renewable energy and greater climate change. A more comprehensive framing of the counterfactual in cumulative ecological impact assessments would evaluate, for each species or system, the incremental effects of renewables over their full life cycle against the incremental effects they provide by mitigating climate change. This framing is important because a given species or system may see net positive or net negative effects from either renewables or climate change. Furthermore, cumulative impact assessments could identify optimized tradeoffs that balance, for each species or system, the effects of both climate change and renewable energy.

Frontiers in Conservation Science↗
USGS2018

Energy allocation and feeding ecology of juvenile chum salmon (Oncorhynchus keta) during transition from freshwater to saltwater

Pacific salmon (Oncorhynchus spp.) populations near their northern range extent in the Arctic-Yukon-Kuskokwim region of Alaska have undergone major changes in population trajectory and illuminated the lack of basic information on juvenile ecology. This study fills information gaps on the early life history of chum salmon at northern latitudes. Energy allocation was examined in the context of distribution, feeding intensity, and diet during a critical life history period for a single cohort of juvenile chum salmon (O. keta) as they transition from freshwater to saltwater in Kuskokwim Bay from mid-May to early June. Juvenile chum salmon were primarily captured in the river mouth and plume. Energy density (kJ g−1 dry mass) was related to fork length, timing (day-of-year), and capture location in a general additive model. The smallest fish had slightly higher energy densities, but the change in energy density with fish size was minimal and consistent with allocating energy toward somatic growth rather than lipid storage. Fish captured earlier had higher energy density, likely reflecting the presence of residual yolk lipids during early migration. Fish captured in the river mouth and plume had higher energy densities. Feeding intensity was highest among small fish captured later within the river plume. Diet was dominated by surface prey (insects and calanoid copepods) rather than epibenthic harpacticoid copepods as commonly observed. These results provide the first data on energy allocation of juvenile chum salmon during a critical life history phase and suggest that somatic growth is prioritized over storing lipid at saltwater entry.

Alaska↗
USGS2006

Energy density of lake whitefish Coregonus clupeaformis in Lakes Huron and Michigan

We collected lake whitefish Coregonus clupeaformis off Alpena and Tawas City, Michigan, USA in Lake Huron and off Muskegon, Michigan USA in Lake Michigan during 2002–2004. We determined energy density and percent dry weight for lake whitefish from both lakes and lipid content for Lake Michigan fish. Energy density increased with increasing fish weight up to 800 g, and then remained relatively constant with further increases in fish weight. Energy density, adjusted for weight, was lower in Lake Huron than in Lake Michigan for both small (≤800 g) and large fish (>800 g). Energy density did not differ seasonally for small or large lake whitefish or between adult male and female fish. Energy density was strongly correlated with percent dry weight and percent lipid content. Based on data from commercially caught lake whitefish, body condition was lower in Lake Huron than Lake Michigan during 1981–2003, indicating that the dissimilarity in body condition between the lakes could be long standing. Energy density and lipid content in 2002–2004 in Lake Michigan were lower than data for comparable sized fish collected in 1969–1971. Differences in energy density between lakes were attributed to variation in diet and prey energy content as well as factors that affect feeding rates such as lake whitefish density and prey abundance.

Environmental Biology of Fishes↗
USGS2013

Fertilizer consumption and energy input for 16 crops in the United States

Fertilizer use by U.S. agriculture has increased over the past few decades. The production and transportation of fertilizers (nitrogen, N; phosphorus, P; potassium, K) are energy intensive. In general, about a third of the total energy input to crop production goes to the production of fertilizers, one-third to mechanization, and one-third to other inputs including labor, transportation, pesticides, and electricity. For some crops, fertilizer is the largest proportion of total energy inputs. Energy required for the production and transportation of fertilizers, as a percentage of total energy input, was determined for 16 crops in the U.S. to be: 19–60% for seven grains, 10–41% for two oilseeds, 25% for potatoes, 12–30% for three vegetables, 2–23% for two fruits, and 3% for dry beans. The harvested-area weighted-average of the fraction of crop fertilizer energy to the total input energy was 28%. The current sources of fertilizers for U.S. agriculture are dependent on imports, availability of natural gas, or limited mineral resources. Given these dependencies plus the high energy costs for fertilizers, an integrated approach for their efficient and sustainable use is needed that will simultaneously maintain or increase crop yields and food quality while decreasing adverse impacts on the environment.

Natural Resources Research↗
USGS1981

Gravitational potential as a source of earthquake energy

Some degree of tectonic stress within the earth originates from gravity acting upon density structures. The work performed by this "gravitational tectonics stress" must have formerly existed as gravitational potential energy contained in the stress-causing density structure. According to the elastic rebound theory (Reid, 1910), the energy of earthquakes comes from an elastic strain field built up by fairly continuous elastic deformation in the period between events. For earthquakes resulting from gravitational tectonic stress, the elastic rebound theory requires the transfer of energy from the gravitational potential of the density structures into an elastic strain field prior to the event. An alternate theory involves partial gravitational collapse of the stress-causing density structures. The earthquake energy comes directly from a net decrease in gravitational potential energy. The gravitational potential energy released at the time of the earthquake is split between the energy released by the earthquake, including work done in the fault zone and an increase in stored elastic strain energy. The stress associated with this elastic strain field should oppose further fault slip.

Alaska↗
USGS2012

Effects of activity and energy budget balancing algorithm on laboratory performance of a fish bioenergetics model

We evaluated the performance of the Wisconsin bioenergetics model for lake trout Salvelinus namaycush that were fed ad libitum in laboratory tanks under regimes of low activity and high activity. In addition, we compared model performance under two different model algorithms: (1) balancing the lake trout energy budget on day t based on lake trout energy density on day t and (2) balancing the lake trout energy budget on day t based on lake trout energy density on day t + 1. Results indicated that the model significantly underestimated consumption for both inactive and active lake trout when algorithm 1 was used and that the degree of underestimation was similar for the two activity levels. In contrast, model performance substantially improved when using algorithm 2, as no detectable bias was found in model predictions of consumption for inactive fish and only a slight degree of overestimation was detected for active fish. The energy budget was accurately balanced by using algorithm 2 but not by using algorithm 1. Based on the results of this study, we recommend the use of algorithm 2 to estimate food consumption by fish in the field. Our study results highlight the importance of accurately accounting for changes in fish energy density when balancing the energy budget; furthermore, these results have implications for the science of evaluating fish bioenergetics model performance and for more accurate estimation of food consumption by fish in the field when fish energy density undergoes relatively rapid changes.

Transactions of the American Fisheries Society↗
USGS2012

Representing the acquisition and use of energy by individuals in agent-based models of animal populations

1. Agent-based models (ABMs) are widely used to predict how populations respond to changing environments. As the availability of food varies in space and time, individuals should have their own energy budgets, but there is no consensus as to how these should be modelled. Here, we use knowledge of physiological ecology to identify major issues confronting the modeller and to make recommendations about how energy budgets for use in ABMs should be constructed. 2. Our proposal is that modelled animals forage as necessary to supply their energy needs for maintenance, growth and reproduction. If there is sufficient energy intake, an animal allocates the energy obtained in the order: maintenance, growth, reproduction, energy storage, until its energy stores reach an optimal level. If there is a shortfall, the priorities for maintenance and growth/reproduction remain the same until reserves fall to a critical threshold below which all are allocated to maintenance. Rates of ingestion and allocation depend on body mass and temperature. We make suggestions for how each of these processes should be modelled mathematically. 3. Mortality rates vary with body mass and temperature according to known relationships, and these can be used to obtain estimates of background mortality rate. 4. If parameter values cannot be obtained directly, then values may provisionally be obtained by parameter borrowing, pattern-oriented modelling, artificial evolution or from allometric equations. 5. The development of ABMs incorporating individual energy budgets is essential for realistic modelling of populations affected by food availability. Such ABMs are already being used to guide conservation planning of nature reserves and shell fisheries, to assess environmental impacts of building proposals including wind farms and highways and to assess the effects on nontarget organisms of chemicals for the control of agricultural pests.

Methods in Ecology and Evolution↗
USGS2024

The geographic extent of bird populations affected by renewable-energy development

Bird populations are declining globally. Wind and solar energy can reduce emissions of fossil fuels that drive anthropogenic climate change, yet renewable-energy production represents a potential threat to bird species. Surveys to assess potential effects at renewable-energy facilities are exclusively local, and the geographic extent encompassed by birds killed at these facilities is largely unknown, which creates challenges for minimizing and mitigating the population-level and cumulative effects of these fatalities. We performed geospatial analyses of stable hydrogen isotope data obtained from feathers of 871 individuals of 24 bird species found dead at solar- and wind-energy facilities in California (USA). Most species had individuals with a mix of origins, ranging from 23% to 98% nonlocal. Mean minimum distances to areas of likely origin for nonlocal individuals were as close as 97 to >1250 km, and these minimum distances were larger for species found at solar-energy facilities in deserts than at wind-energy facilities in grasslands (Cohen's d = 6.5). Fatalities were drawn from an estimated 30–100% of species’ desingated ranges, and this percentage was significantly smaller for species with large ranges found at wind facilities (Pearson's r = −0.67). Temporal patterns in the geographic origin of fatalities suggested that migratory movements and nonmigratory movements, such as dispersal and nomadism, influence exposure to fatality risk for these birds. Our results illustrate the power of using stable isotope data to assess the geographic extent of renewable-energy fatalities on birds. As the buildout of renewable-energy facilities continues, accurate assessment of the geographic footprint of wildlife fatalities can be used to inform compensatory mitigation for their population-level and cumulative effects.

Conservation Biology↗
USGS2021

Direct and size-mediated effects of temperature and ration-dependent growth rates on energy reserves in juvenile anadromous alewives (Alosa pseudoharengus)

Growth rate and energy reserves are important determinants of fitness and are governed by endogenous and exogenous factors. Thus, examining the influence of individual and multiple stressors on growth and energy reserves can help estimate population health under current and future conditions. In young anadromous fishes, freshwater habitat quality determines physiological state and fitness of juveniles emigrating to marine habitats. We tested how temperature and food availability affect survival, growth, and energy reserves in juvenile anadromous alewives ( Alosa pseudoharengus ), a forage fish distributed along the eastern North American continent. Field-collected juvenile anadromous A. pseudoharengus were exposed for 21 days to one of two temperatures (21°C and 25°C) and one of two levels of food rations (1% or 2% tank biomass daily) and compared for differences in final size, fat mass-at-length, lean mass-at-length, and energy density. Increased temperature and reduced ration both led to lower growth rates and the effect of reduced ration was greater at higher temperature. Fat mass-at-length decreased with dry mass and energy density increased with total length, suggesting size-based endogenous influences on energy reserves. Lower ration also directly decreased fat mass-at-length, lean mass-at-length and energy density. Given the fitness implications of size and energy reserves, temperature and food availability should be considered important indicators of nursery habitat quality and incorporated in A. pseudoharengus life history models to improve forecasting of population health under climate change.

Journal of Fish Biology↗
USGS2004

Radiated energy and the rupture process of the Denali fault earthquake sequence of 2002 from broadband teleseismic body waves

Displacement, velocity, and velocity-squared records of P and SH body waves recorded at teleseismic distances are analyzed to determine the rupture characteristics of the Denali fault, Alaska, earthquake of 3 November 2002 ( M W 7.9, M e 8.1 ). Three episodes of rupture can be identified from broadband ( ∼0.1–5.0 Hz ) waveforms. The Denali fault earthquake started as a M W 7.3 thrust event. Subsequent right-lateral strike-slip rupture events with centroid depths of 9 km occurred about 22 and 49 sec later. The teleseismic P waves are dominated by energy at intermediate frequencies (0.1-1 Hz) radiated by the thrust event, while the SH waves are dominated by energy at lower frequencies (0.05-0.2 Hz) radiated by the strike-slip events. The strike-slip events exhibit strong directivity in the teleseismic SH waves. Correcting the recorded P -wave acceleration spectra for the effect of the free surface yields an estimate of 2.8 × 10 15 N m for the energy radiated by the thrust event. Correcting the recorded SH -wave acceleration spectra similarly yields an estimate of 3.3 × 10 16 N m for the energy radiated by the two strike-slip events. The average rupture velocity for the strike-slip rupture process is 1.1 β –1.2 β . The strike-slip events were located 90 and 188 km east of the epicenter. The rupture length over which significant or resolvable energy is radiated is, thus, far shorter than the 340-km fault length over which surface displacements were observed. However, the seismic moment released by these three events, 4 × 10 20 N m, was approximately half the seismic moment determined from very low-frequency analyses of the earthquake. The difference in seismic moment can be reasonably attributed to slip on fault segments that did not radiate significant or coherent seismic energy. These results suggest that very large and great strike-slip earthquakes can generate stress pulses that rapidly produce substantial slip with negligible stress drop and little discernible radiated energy on fault segments distant from the initial point of nucleation. The existence of this energy-deficient rupture mode has important implications for the evaluation of the seismic hazard of very large strike-slip earthquakes.

Alaska↗
USGS2014

Nearshore energy subsidies support Lake Michigan fishes and invertebrates following major changes in food web structure

Aquatic food webs that incorporate multiple energy channels (e.g. nearshore benthic or pelagic) with varying productivity and turnover rates convey stability to biological communities by providing multiple independent energy sources. Within the Lake Michigan food web, invasive dreissenid mussels have caused rapid changes to food web structure and potentially altered the channels through which consumers acquire energy. We used stable C and N isotopes to determine how Lake Michigan food web structure has changed in the past decade, coincident with the expansion of dreissenid mussels, decreased pelagic phytoplankton production and increased nearshore benthic algal production. Fish and invertebrate samples collected from sites around Lake Michigan were analyzed to determine taxa-specific 13C:12C (delta 13C) and 15N:14N (delta 15N) ratios. Sampling took place during two distinct periods, 2002-2003 and 2010-2012, that spanned the period of dreissenid expansion, and included nearshore, pelagic and profundal fish and invertebrate taxa. Magnitude and direction of the 13C shift indicated significantly greater reliance upon nearshore benthic energy sources among nearly all fish taxa as well as profundal invertebrates. Although the mechanisms underlying this 13C shift likely varied among species, possible causes include the transport of benthic algal production to offshore waters and an increased reliance on nearshore prey items. Delta 15N shifts were more variable and of smaller magnitude across taxa although declines in delta 15N among some pelagic fishes may indicate a shift to alternative prey resources. Lake Michigan fishes and invertebrates appear to have responded to dreissenid induced changes in nutrient and energy pathways by switching from pelagic to alternative nearshore energy subsidies. Although large shifts in energy allocation (i.e. pelagic to nearshore benthic) resulting from invasive species appear to have affected total production at upper trophic levels, changes in trophic structure and utilization of novel energy pathways may help to stabilize food webs following species invasions.

Lake Michigan↗
USGS2018

U.S. Geological Survey energy and wildlife research annual report for 2018

USGS scientists provide scientific information and options that land and resource managers and private industries can use to make decisions regarding the development of energy resources while protecting the health of ecosystems. Studies focus on delivering information to avoid, minimize, or mitigate the impacts of energy infrastructure on fish and wildlife. USGS scientists are currently developing mapping tools and models that identify areas of biological strengths and weaknesses or high- and low-quality habitat and can identify opportunities for conservation—areas of high-quality habitat where energy-generating potential is low—and areas of potential risk—areas of high-quality habitat where energy-generating potential is high. These tools can assist resource managers and the industry concerning siting of energy development and selection of off-site mitigation areas. Scientific efforts, such as these, further the understanding of impacts related to energy development and create workable solutions. The three goals guiding USGS activities related to the interactions between wildlife and energy development are to understand risks by identifying when, where, and how fish and wildlife share space with energy facilities, measure direct and indirect impacts to species, and inform feasible and cost-effective solutions to minimize impacts through technological fixes, management, and mitigation.

Circular↗
USGS2016

U.S. Geological Survey—Energy and Wildlife Research Annual Report for 2016

Recent growth and development of renewable energy and unconventional oil and gas extraction are rapidly diversifying the energy supply of the United States. Yet, as our Nation works to advance energy security and conserve wildlife, some conflicts have surfaced. To address these challenges, the U.S. Geological Survey (USGS) is conducting innovative research and developing workable solutions to reduce the impacts of energy production on wildlife. USGS scientists collaborate on many studies with scientists from other Federal, State, and local government agencies; Tribal nations; academic research institutions; and nongovernmental and private organizations. The mix of fuels used for electricity generation is evolving. Solar, natural gas, and wind energy made up most electricity generation additions in 2015 and 2016. The United States now leads the world in natural gas production, with new record highs for each year from 2011 through 2015. More than 48,000 wind turbines now contribute to power grids in most States, providing about 5 percent of U.S. end-use electricity demand in an average year. The number of utility-scale solar-energy projects is growing rapidly with solar energy projected to contribute to the largest electricity generation addition in 2016. A substantial number of large energy projects have been constructed on undeveloped public lands, and more are anticipated at an increasing rate, creating new stress to wildlife. Direct impacts include collisions with wind turbines and structures at solar facilities and loss of habitat which may negatively affect sensitive species. Recent estimates suggest 250,000 to 500,000 birds die each year at wind turbine facilities. Bat fatality rates at wind turbine facilities are less certain, but may average several hundred thousand per year throughout North America. Because new projects may be located in or near sensitive wildlife habitats, ecological science plays a key role in helping to guide project siting and operational decisions.

Open-File Report↗
USGS2019

Energy depletion and stress levels of Sockeye Salmon migrating at the northern edge of their distribution

The physiological challenge for anadromous fish to migrate upriver is influenced by river temperature, but the impacts of river temperature can be difficult to predict due to an incomplete understanding of how temperature influences migration costs, especially in high‐latitude (>60°N) ecosystems. To assess temperature influences on migrating Pacific salmon Oncorhynchus spp., we measured heat shock protein 70 (HSP70), as an indicator of cellular stress, and energy content of Sockeye Salmon Oncorhynchus nerka throughout their upriver migration in the Pilgrim River, Alaska. Although HSP70 was elevated as fish moved to the spawning grounds and was higher in fish with low energy content, HSP70 did not increase with warmer river temperatures. We verified in an experiment that HSP70 abundance in Sockeye Salmon does respond to temperatures above 20.5°C. Over the 4 years of sampling, energy content decreased at similar rates as Sockeye Salmon moved upstream. We expected Sockeye Salmon energy levels would be lower when migrating in warmer river temperatures; however, we found higher energy levels occurred with higher temperatures in the Pilgrim River. We hypothesize that the relationship between temperature and energy content is due to river temperatures often occurring below optimal temperatures for migration. Lower temperatures could be energetically costly or reduce migration rates, both of which would result in lower energy content with cooler temperature. Understanding interactions between environmental drivers and physiological responses will help managers anticipate future changes for Sockeye Salmon at the northern edge of their distribution.

Alaska↗
USGS2007

Net energy payback and CO2 emissions from three midwestern wind farms: An update

This paper updates a life-cycle net energy analysis and carbon dioxide emissions analysis of three Midwestern utility-scale wind systems. Both the Energy Payback Ratio (EPR) and CO2 analysis results provide useful data for policy discussions regarding an efficient and low-carbon energy mix. The EPR is the amount of electrical energy produced for the lifetime of the power plant divided by the total amount of energy required to procure and transport the materials, build, operate, and decommission the power plants. The CO2 analysis for each power plant was calculated from the life-cycle energy input data. A previous study also analyzed coal and nuclear fission power plants. At the time of that study, two of the three wind systems had less than a full year of generation data to project the life-cycle energy production. This study updates the analysis of three wind systems with an additional four to eight years of operating data. The EPR for the utility-scale wind systems ranges from a low of 11 for a two-turbine system in Wisconsin to 28 for a 143-turbine system in southwestern Minnesota. The EPR is 11 for coal, 25 for fission with gas centrifuge enriched uranium and 7 for gaseous diffusion enriched uranium. The normalized CO2 emissions, in tonnes of CO2 per GW eh, ranges from 14 to 33 for the wind systems, 974 for coal, and 10 and 34 for nuclear fission using gas centrifuge and gaseous diffusion enriched uranium, respectively. ?? Springer Science+Business Media, LLC 2007.

Natural Resources Research↗
USGS1978

Revised values for the Gibbs free energy of formation of [Al(OH)4 aq-], diaspore, boehmite and bayerite at 298.15 K and 1 bar, the thermodynamic properties of kaolinite to 800 K and 1 bar, and the heats of solution of several gibbsite samples

Solution calorimetric measurements compared with solubility determinations from the literature for the same samples of gibbsite have provided a direct thermochemical cycle through which the Gibbs free energy of formation of [Al(OH) 4 aq − ] can be determined. The Gibbs free energy of formation of [Al(OH) 4 aq − ] at 298.15 K is −1305 ± 1 kJ/mol. These heat-of-solution results show no significant difference in the thermodynamic properties of gibbsite particles in the range from 50 to 0.05 μm. The Gibbs free energies of formation at 298.15 K and 1 bar pressure of diaspore, boehmite and bayerite are −9210 ± 5.0, −918.4 ± 2.1 and −1153 ± 2 kJ/mol based upon the Gibbs free energy of [A1(OH) 4 aq − ] calculated in this paper and the acceptance of −1582.2 ± 1.3 and −1154.9 ± 1.2 kJ/mol for the Gibbs free energy of formation of corundum and gibbsite, respectively. Values for the Gibbs free energy formation of [Al(OH) 2 aq + ] and [AlO 2 aq − ] were also calculated as −914.2 ± 2.1 and −830.9 ± 2.1 kJ/mol, respectively. The use of [AlC 2 aq − ] as a chemical species is discouraged. A revised Gibbs free energy of formation for [H 4 SiO 4aq 0 ] was recalculated from calorimetric data yielding a value of −1307.5 ± 1.7 kJ/mol which is in good agreement with the results obtained from several solubility studies. Smoothed values for the thermodynamic functions C P 0 , ( H T 0 - H 298 0 ) T "> HT0- H2980)T , ( G T 0 - H 298 0 ) T "> (GT0- H2980)T , S T 0 - S 0 0 , ΔH ƒ,298 0 ">ƒ ΔHƒ,2980 kaolinite are listed at integral temperatures between 298.15 and 800 K. The heat capacity of kaolinite at temperatures between 250 and 800 K may be calculated from the following equation: C P 0 = 1430.26 − 0.78850 T + 3.0340 × 10 −4 T 2 −1.85158 × 10 −4 T 2 1 2 + 8.3341 × 10 6 T −2 "> 12+ 8.3341 × 106T−2 . The thermodynamic properties of most of the geologically important Al-bearing phases have been referenced to the same reference state for Al, namely gibbsite.

Geochimica et Cosmochimica Acta↗