USGS Science⌕ Search

SEARCH · USGS Science

Results for “Trout”

Search indexed USGS publications on groundwater, aquifers, geologic maps, mineral resources and earthquakes. Explore source records by subject and place.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 1,711 records · Page 95Linked to original sources

Status of Cisco in Lake Superior in 2017

This report describes the status of fish species and their habitat in Lake Superior during the reporting period of 2012-2016 in response to achievement of fish community objectives (FCOs) established by fishery managers for the lake. The overarching goal for the FCOs continued to be met as the fish community remained diverse, self-regulating, dominated by indigenous species, and able to support sustainable fisheries, although further rehabilitation of certain fish is required. The Lake Superior Lakewide Action and Management Plan classified all habitat indicators for Lake Superior as good. Primary production and zooplankton abundance were stable during the reporting period and unchanged from the two previous reporting periods, indicating the lower food web is healthy. Abundance of the invertebrates Mysis diluviana and Diporeia spp. were stable during the reporting period, and Diporeia spp. density exceeded target levels defined in the Great Lakes Water Quality Agreement. Lake Whitefish (Coregonus clupeaformis) abundance was lower than during the previous reporting period but was within the FCO target. Abundance of lean, siscowet, and humper forms of Lake Trout (Salvelinus namaycush) remained stable at levels seen in previous reporting periods. The FCO for non-indigenous salmonids was met as Chinook Salmon (Oncorhynchus tshawytscha), Coho Salmon (O. kisutch), and steelhead/Rainbow Trout (O. mykiss) were being sustained by natural reproduction, and their abundance remained stable or increased from previous reporting periods. The FCO for Walleye (Sander vitreus) was not met, although populations showed signs of improvement since the previous reporting period. The fish community in littoral areas and embayments continued to be diverse and composed mostly of indigenous species. No new invasive species were found in Lake Superior during the reporting period. Degraded embayment and tributary habitats continued to prevent achievement of the FCOs for Brook Trout (S. fontinalis) and Lake Sturgeon (Acipenser fulvescens). Barriers created for hydroelectric generation either blocked Lake Sturgeon from historically important spawning grounds or reduced stream flows necessary for its reproduction. In tributaries without man-made barriers, Lake Sturgeon was relatively abundant and appeared healthy. Attainment of the FCOs for Brook Trout and Lake Sturgeon will be challenging and can only be attained through development of large-scale management actions like those implemented for Lake Trout rehabilitation and Sea Lamprey (Petromyzon marinus) control. Sea Lamprey-control expenditures doubled in 2016 from past levels and should result in suppression of the population closer to its FCO after 2016. The prey-fish FCO appears to have been met, but biomass of nearly all prey-fish species declined from that reported for the previous reporting period and has been on a downward trajectory since 2000. Predation by Lake Trout is probably to blame for the declining biomass of prey fish. Poor recruitment by Cisco (C. artedi) over the last 15 years is exacerbating the declines in prey-fish biomass because Lake Trout must compensate for the loss of Cisco by consuming other, less-abundant prey fish.

Lake Superior↗

State of Lake Superior ecosystem in 2017

This report describes the status of fish species and their habitat in Lake Superior during the reporting period of 2012-2016 in response to achievement of fish community objectives (FCOs) established by fishery managers for the lake. The overarching goal for the FCOs continued to be met as the fish community remained diverse, self-regulating, dominated by indigenous species, and able to support sustainable fisheries, although further rehabilitation of certain fish is required. The Lake Superior Lakewide Action and Management Plan classified all habitat indicators for Lake Superior as good. Primary production and zooplankton abundance were stable during the reporting period and unchanged from the two previous reporting periods, indicating the lower food web is healthy. Abundance of the invertebrates Mysis diluviana and Diporeia spp. were stable during the reporting period, and Diporeia spp. density exceeded target levels defined in the Great Lakes Water Quality Agreement. Lake Whitefish (Coregonus clupeaformis) abundance was lower than during the previous reporting period but was within the FCO target. Abundance of lean, siscowet, and humper forms of Lake Trout (Salvelinus namaycush) remained stable at levels seen in previous reporting periods. The FCO for non-indigenous salmonids was met as Chinook Salmon (Oncorhynchus tshawytscha), Coho Salmon (O. kisutch), and steelhead/Rainbow Trout (O. mykiss) were being sustained by natural reproduction, and their abundance remained stable or increased from previous reporting periods. The FCO for Walleye (Sander vitreus) was not met, although populations showed signs of improvement since the previous reporting period. The fish community in littoral areas and embayments continued to be diverse and composed mostly of indigenous species. No new invasive species were found in Lake Superior during the reporting period. Degraded embayment and tributary habitats continued to prevent achievement of the FCOs for Brook Trout (S. fontinalis) and Lake Sturgeon (Acipenser fulvescens). Barriers created for hydroelectric generation either blocked Lake Sturgeon from historically important spawning grounds or reduced stream flows necessary for its reproduction. In tributaries without man-made barriers, Lake Sturgeon was relatively abundant and appeared healthy. Attainment of the FCOs for Brook Trout and Lake Sturgeon will be challenging and can only be attained through development of large-scale management actions like those implemented for Lake Trout rehabilitation and Sea Lamprey (Petromyzon marinus) control. Sea Lamprey-control expenditures doubled in 2016 from past levels and should result in suppression of the population closer to its FCO after 2016. The prey-fish FCO appears to have been met, but biomass of nearly all prey-fish species declined from that reported for the previous reporting period and has been on a downward trajectory since 2000. Predation by Lake Trout is probably to blame for the declining biomass of prey fish. Poor recruitment by Cisco (C. artedi) over the last 15 years is exacerbating the declines in prey-fish biomass because Lake Trout must compensate for the loss of Cisco by consuming other, less-abundant prey fish.

Lake Superior↗

Water temperature analysis of the North Branch Au Sable River, Michigan, and implications to salmonid populations

Ambient stream water temperatures affect salmonid movement and survival with fish actively seeking thermal refugia from warming waters. This study sought to investigate the potential role of water temperature in the perceived decline in native Brook Trout Salvelinus fontinalis and non-native Brown Trout Salmo trutta populations in the North Branch Au Sable River by fishers and reported to resource managers in 2018 and 2019. Water temperature was analyzed at nine stations within the North Branch Au Sable River in 2021 and 2022. A total of 61,390 temperature observations were collected with 58.0% exceeding the optimal growth threshold for Brook Trout of 16°C; 37.9% exceeding the movement threshold for Brook Trout of 18°C; 3.4% exceeding the upper limit for positive growth for Brook Trout of 23.4°C; and 28.6% exceeding the optimal growth threshold for Brown Trout of 19°C. The maximum daily water temperatures recorded for each year were 27.58°C in 2021 and 26.89°C in 2022. The availability of cold water thermal refugia is critical to the viability of native Brook Trout populations in the North Branch Au Sable River and its tributaries. Efforts should be taken to increase ambient stream water temperature monitoring year-round and to determine the size, frequency, and availability of thermal refugia within the watershed to increase the likelihood of a system resilient to the impacts of a warming climate.

Michigan↗

Effects of summer air exposure on the survival of caught-and-released salmonids

Despite the success of catch‐and‐release regulations, exposing fish to air during release has emerged as a growing concern over the past two decades. We evaluated the effect of air exposure during midsummer on survival of Yellowstone Cutthroat Trout Oncorhynchus clarkii bouvieri , Bull Trout Salvelinus confluentus , and Rainbow Trout O. mykiss exposed to catch‐and‐release angling. Fish were sampled by angling on Palisades Creek (August 2016), Sawmill Creek, and the Main Fork of the Little Lost River, Idaho (July−August 2017). After capture, fish were kept underwater while they were measured and individually tagged. Anglers, in groups of two to four, caught study fish and gave them an air exposure treatment of 0, 30, or 60 s. Single‐pass backpack electrofishing was then used to recapture tagged fish and estimate relative survival. In total, 328 Yellowstone Cutthroat Trout were sampled (0 s: n = 110; 30 s: n = 110; 60 s: n = 108), 278 Bull Trout (0 s: n = 92; 30 s: n = 94; 60 s: n = 92), and 322 Rainbow Trout (0 s: n = 103; 30 s: n = 106; 60 s: n = 113). The majority of fish were caught using artificial flies (≥92%) and were hooked in the corner of the mouth, lower jaw, or upper jaw (≥78%) in all three species. No difference in survival was observed among air exposure treatments for all three species. Results from the present study along with those from prior field studies of air exposure times during angling suggest that mortality from exposing fish to air for ≤60 s is not likely a population‐level concern in catch‐and‐release fisheries for these species.

Idaho↗

Abiotic & biotic responses of the Colorado River to controlled floods at Glen Canyon Dam, Arizona, USA

Closure of Glen Canyon Dam reduced sand supply to the Colorado River in Grand Canyon National Park by about 94% while its operation has also eroded the park's sandbar habitats. Three controlled floods released from the dam since 1995 suggest that sandbars might be rebuilt and maintained, but only if repeated floods are timed to follow tributary sand deliveries below the dam. Monitoring data show that sandbars are dynamic and that their erosion after bar building is positively related with mean daily discharge and negatively related with tributary sand production after controlled floods. The March 2008 flood affected non-native rainbow trout abundance in the Lees Ferry tailwater, which supports a blue ribbon fishery. Downstream trout dispersal from the tailwater results in negative competitive interactions and predation on endangered humpback chub. Early survival rates of age-0 trout increased more than fourfold following the 2008 flood, and twofold in 2009, relative to prior years (2006-2007). Hatch-date analysis indicated that early survival rates were much higher for cohorts that emerged about 2 months after the 2008 flood relative to cohorts that emerged earlier that year. The 2009 survival data suggest that tailwater habitat improvements persisted for at least a year, but apparently decreased in 2010. Increased early survival rates for trout coincided with the increased availability of higher quality drifting food items after the 2008 flood owing to an increase in midges and black flies, preferred food items of rainbow trout. Repeated floods from the dam might sustainably rebuild and maintain sandbars if released when new tributary sand is available below the tailwater. Spring flooding might also sustain increased trout abundance and benefit the tailwater fishery, but also be a potential risk to humpback chub in Grand Canyon.

Arizona;Nevada;Utah↗

A comparative examination of cortisol effects on muscle myostatin and HSP90 gene expression in salmonids

Cortisol, the primary corticosteroid in teleost fishes, is released in response to stressors to elicit local functions, however little is understood regarding muscle-specific responses to cortisol in these fishes. In mammals, glucocorticoids strongly regulate the muscle growth inhibitor, myostatin, via glucocorticoid response elements (GREs) leading to muscle atrophy. Bioinformatics methods suggest that this regulatory mechanism is conserved among vertebrates, however recent evidence suggests some fishes exhibit divergent regulation. Therefore, the aim of this study was to evaluate the conserved actions of cortisol on myostatin and hsp90 expression to determine if variations in cortisol interactions have emerged in salmonid species. Representative salmonids; Chinook salmon (Oncorhynchus tshawytscha), cutthroat trout (Oncorhynchus clarki), brook trout (Salvelinus fontinalis), and Atlantic salmon (Salmo salar); were injected intraperitoneally with a cortisol implant (50 lg/g body weight) and muscle gene expression was quantified after 48 h. Plasma glucose and cortisol levels were significantly elevated by cortisol in all species, demonstrating physiological effectiveness of the treatment. HSP90 mRNA levels were elevated by cortisol in brook trout, Chinook salmon, and Atlantic salmon, but were decreased in cutthroat trout. Myostatin mRNA levels were affected in a species, tissue (muscle type), and paralog specific manner. Cortisol treatment increased myostatin expression in brook trout (Salvelinus) and Atlantic salmon (Salmo), but not in Chinook salmon (Oncorhynchus) or cutthroat trout (Oncorhynchus). Interestingly, the VC alone increased myostatin mRNA expression in Chinook and Atlantic salmon, while the addition of cortisol blocked the response. Taken together, these results suggest that cortisol affects muscle-specific gene expression in species-specific manners, with unique Oncorhynchus-specific divergence observed, that are not predictive solely based upon mammalian stress responses.

General and Comparative Endocrinology↗

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↗

Modeling prey consumption by native and non-native piscivorous fishes: implications for competition and impacts on shared prey in an ultraoligotrophic lake in Patagonia

We examined trophic interactions of the nonnative salmonids Rainbow Trout Oncorhynchus mykiss, Brown Trout Salmo trutta, and Brook Trout Salvelinus fontinalisand the main native predator Creole Perch Percichthys trucha in Lake Nahuel Huapi (Patagonia, Argentina) to determine the relative impact of each predator on their forage base and to evaluate the potential vulnerability of each predator to competitive impacts by the others. Using bioenergetics simulations, we demonstrated the overall importance of galaxiids and decapods to the energy budgets of nonnative salmonids and Creole Perch. Introduced salmonids, especially Rainbow Trout, exerted considerably heavier predatory demands on shared resources than did the native Creole Perch on both a per capita basis and in terms of relative population impacts. Rainbow Trout consumed higher quantities and a wider size range of Small Puyen (also known as Inanga) Galaxias maculatus than the other predators, including early pelagic life stages of that prey; as such, this represents an additional source of mortality for the vulnerable early life stages of Small Puyen before and during their transition from pelagic to benthic habitats. All predators were generally feeding at high feeding rates (above 40% of their maximum physiological rates), suggesting that competition for prey does not currently limit either Creole Perch or the salmonids in this lake. This study highlights the importance of keystone prey for the coexistence of native species with nonnative top predators. It provides new quantitative and qualitative evidence of the high predation pressure exerted on Small Puyen, the keystone prey species, during the larval to juvenile transition from pelagic to littoral-benthic habitat in Patagonian lakes. This study also emphasizes the importance of monitoring salmonid and Creole Perch population dynamics in order to detect signs of potential impacts through competition and shows the need to carefully consider the rationale behind any additional trout stocking.

Transactions of the American Fisheries Society↗

Response of nutrient limitation to invasive fish suppression: How carcasses and analog pellets alter periphyton

The native Yellowstone Cutthroat Trout ( Oncorhynchus clarkii bouvieri Jordan and Gilbert, 1883) population in Yellowstone Lake, Yellowstone National Park, Wyoming, USA, is in decline because of competition from the introduced, invasive Lake Trout ( Salvelinus namaycush Walbaum in Artedi, 1792). Gillnetting is used to suppress adult Lake Trout; however, methods are being developed to suppress embryos, including adding Lake Trout carcasses and carcass-analog pellets to spawning sites. Decomposing carcasses and analog pellets cause decreased dissolved oxygen concentrations thereby leading to Lake Trout embryo mortality, but the effects of these methods on primary producers are unknown. We deployed in-situ nutrient diffusing substrates (NDS) at 3 spawning sites. The 1 st site was treated with carcasses, the 2 nd site was treated with analog pellets, and a 3 rd lacked treatment (control). To estimate how suppression measures may alter nutrient limitation, we measured algal biomass in 6 NDS amendments at each site: nothing (control), N, P, N + P, ground carcasses, or pulverized analog pellets. We deployed 5 replicates of each amendment at each site before and after treating whole sites. N and P co-limited periphyton before carcasses or analog pellets were added to spawning sites ( p < 0.01); however, nutrients were not limiting after the treatments were added to spawning sites ( p = 0.31–1). Algal biomass was 4× higher after whole-site carcass treatments. In contrast, analog pellets appeared to suppress algal biomass in the amendments (20% of NDS at the control site post-treatment) and in the treatment plot (33% of pre-treatment biomass at analog pellet site). We also measured how individual ingredients in analog pellets altered periphyton biomass, which suggested that vitamin E, estrogen, and soybean oil ingredients reduced the growth of primary producers. Suppression methods may stimulate or reduce algal biomass, depending on the methods used, which could have cascading effects on food webs and potentially reduce the success of the control measures. Estimating how different Lake Trout suppression methods may alter basal resources in the littoral zone of Yellowstone Lake will help natural resource agencies develop effective plans to control invasive predators at early life stages while minimally altering ecosystems.

Wyoming↗

A riverscape perspective of Pacific salmonids and aquatic habitats prior to large-scale dam removal in the Elwha River, Washington, USA

Dam removal has been increasingly proposed as a river restoration technique. In 2011, two large hydroelectric dams will be removed from Washington State&rsquo;s Elwha River. Ten anadromous fish populations are expected to recolonise historical habitats after dam removal. A key to understanding watershed recolonisation is the collection of spatially continuous information on fish and aquatic habitats. A riverscape approach with an emphasis on biological data has rarely been applied in mid-sized, wilderness rivers, particularly in consecutive years prior to dam removal. Concurrent snorkel and habitat surveys were conducted from the headwaters to the mouth (rkm 65&ndash;0) of the Elwha River in 2007 and 2008. This riverscape approach characterised the spatial extent, assemblage structure and patterns of relative density of Pacific salmonids. The presence of dams influenced the longitudinal patterns of fish assemblages, and species richness was the highest downstream of the dams, where anadromous salmonids still have access. The percent composition of salmonids was similar in both years for rainbow trout, Oncorhynchus mykiss (Walbaum), coastal cutthroat trout, Oncorhynchus clarkii clarkii (Richardson) (89%; 88%), Chinook salmon, Oncorhynchus tshawytscha (Walbaum) (8%; 9%), and bull trout, Salvelinus confluentus (Suckley) (3% in both years). Spatial patterns of abundance for rainbow and cutthroat trout ( r = 0.76) and bull trout ( r = 0.70) were also consistent between years. Multivariate and univariate methods detected differences in habitat structure along the river profile caused by natural and anthropogenic factors. The riverscape view highlighted species-specific biological hotspots and revealed that 60&ndash;69% of federally threatened bull trout occurred near or below the dams. Spatially continuous surveys will be vital in evaluating the effectiveness of upcoming dam removal projects at restoring anadromous salmonids.

Washington↗

Life-history variation of two inland salmonids revealed through otolith microchemistry analysis

Increasingly, otolith microchemistry analysis is used as a tool to trace fish migrations, especially migrations of diadromous fishes. Yet, few studies have used otolith microchemistry to trace migrations in small inland watersheds, leaving major knowledge gaps in our understanding of inland fish spatial ecology. Here, we evaluate the use of tributary habitat for spawning and describe and compare fluvial brown trout ( Salmo trutta ) and rainbow trout ( Oncorhynchus mykiss ) natal origin distribution, time spent in natal streams, and spawning site fidelity. 63% of rainbow trout and 57% of brown trout migrated after hatching. Brown trout showed greater variation in time spent in natal tributaries, suggesting that individuals are temporally distributing risk among offspring. By contrast, rainbow trout showed greater variation in natal origin, suggesting that individuals are spatially distributing risk among offspring. Our results indicate there is high inter- and intraspecific migration variation in inland salmonid populations, which may be linked to access to a mosaic of spawning and rearing habitat types.

Colorado, Wyoming↗

Spatiotemporal patterns in trophic niche overlap among five salmonines in Lake Michigan, USA

Native lake trout and introduced Chinook salmon, coho salmon, steelhead, and brown trout are major predators in Lake Michigan’s complex ecosystem and collectively support a valuable recreational fishery, but declines in their primary prey, alewife, have raised ecological and management concerns about competition and prey allocation. We applied niche overlap analysis to evaluate competition among salmonine predators during rapid forage base change in Lake Michigan. δ13C and δ15N stable isotope ratios indicated that lake trout had a unique trophic niche from inclusion of offshore and benthic prey, with <29% lakewide niche overlap with Chinook salmon, coho salmon and steelhead. Brown trout had moderate overlap with other species (45 – 91%), while Chinook salmon, coho salmon, and steelhead had high overlap (71 – 98%). Regional differences in isotopic signatures highlighted the potential importance of sub-system differences in fish diets in large aquatic systems. The uniqueness of the lake trout niche, and broadness of brown trout and steelhead niches, suggest these species may be resilient to forage base changes. This study demonstrates how niche overlap analysis can be applied to tease apart competitive interactions and their response to ecosystem change.

Lake Michigan↗

Conflicts among protected native birds and valuable sport fishes: Potential pelican predation effects

Reservoirs are examples of novel ecosystems that have developed into popular sport fisheries; these systems are also becoming seasonal refuges for migratory birds, including the piscivorous American white pelican ( Pelecanus erythrorhynchos ). We (1) investigated the proportion of cutthroat trout ( Oncorhynchus clarkii utah ) and other species consumed by pelicans, (2) compared whether pelicans have an adverse effect on cutthroat trout spawning movement, and (3) determined the importance of pelican predation relative to other sources of fish mortality in Strawberry Reservoir, Utah, USA. Pelican diet samples consisted of >85% Utah sucker ( Catostomus ardens ), 6% Utah chub ( Gila atraria ), and 3% cutthroat trout. Based on bioenergetics, we estimated that pelicans consumed 384–3020 individual cutthroat trout (0.17%–1.3% of population), in contrast to 14 166–27 196 nongame sucker and chub. Bird-related mortality rate ranged from 1% to 6% for stocked, PIT (passive integrated transponder)-tagged adult cutthroat trout and from 4% to 16% for subadult cutthroat trout. Based on these results, any management action taken to control pelican predation would need to be weighed against the benefits of nongame fish removal and the protected status of pelicans.

Utah↗

Role of habitat complexity in predator-prey dynamics between an introduced fish and larval Long-toed Salamanders ( Ambystoma macrodactylum )

Predation by nonnative fishes has reduced abundance and increased extinction risk for amphibian populations worldwide. Although rare, fish and palatable amphibians have been observed to coexist where aquatic vegetation and structural complexity provide suitable refugia. We examined whether larval long-toed salamanders ( Ambystoma macrodactylum Baird, 1849) increased use of vegetation cover in lakes with trout and whether adding vegetation structure could reduce predation risk and nonconsumptive effects (NCEs), such as reductions in body size and delayed metamorphosis. We compared use of vegetation cover by larval salamanders in lakes with and without trout and conducted a field experiment to investigate the influence of added vegetation structure on salamander body morphology and life history. The probability of catching salamanders in traps in lakes with trout was positively correlated with the proportion of submerged vegetation and surface cover. Growth rates of salamanders in enclosures with trout cues decreased as much as 85% and the probability of metamorphosis decreased by 56%. We did not find evidence that adding vegetation reduced NCEs in experimental enclosures, but salamanders in lakes with trout utilized more highly-vegetated areas which suggests that adding vegetation structure at the scale of the whole lake may facilitate coexistence between salamanders and introduced trout.

Canadian Journal of Zoology↗

Characterizing aquatic health using salmonid mortality, physiology, and biomass estimates in streams with elevated concentrations of arsenic, cadmium, copper, lead, and zinc in the Boulder River Watershed, Montana

Abandoned tailings and mine adits are located throughout the Boulder River watershed in Montana. In this watershed, all species of fish are absent from some tributary reaches near mine sources; however, populations of brook trout Salvelinus fontitalis , rainbow trout Oncorhynchus mykiss , and cut-throat trout O. clarki are found further downstream. Multiple methods must be used to investigate the effects of metals released by past mining activity because the effects on aquatic life may range in severity, depending on the proximity of mine sources. Therefore, we used three types of effects—those on fish population levels (as measured by survival), those on biomass and density, and those at the level of the individual (as measured by increases in metallothionein, products of lipid peroxidation, and increases in concentrations of tissue metals)—to assess the aquatic health of the Boulder River watershed. Elevated concentrations of Cd, Cu, and Zn in the water column were associated with increased mortality of trout at sites located near mine waste sources. The hypertrophy (swelling), degeneration (dying), and necrosis of epithelial cells observed in the gills support our conclusion that the cause of death was related to metals in the water column. At a site further downstream (lower Cataract Creek), we observed impaired health of resident trout, as well as effects on biomass and density (measured as decreases in the kilograms of trout per hectare and the number per 300 m) and effects at the individual level, including increases in metallothionein, products of lipid peroxidation, and tissue concentrations of metals.

Transactions of the American Fisheries Society↗

Virulence of Renibacterium salmoninarum to salmonids

Virulence of Renibacterium salmoninarum isolates representing five origins was evaluated in eight salmonid hosts; four origins were of Lake Michigan and the fifth was of the Pacific Northwest. The species type strain, ATCC (American Type Culture Collection) 33209, was also included. Each isolate was grown in a kidney disease medium (KDM2) supplemented with 1 % ATCC 33209 culture metabolite; serial 10-fold dilutions were prepared, and groups of fish were challenged by intraperitoneal injection with 0.1 mL of each dilution. A 70-d observation period followed, and bacterial kidney disease (BKD) was diagnosed by the fluorescent antibody technique. Virulence of isolates was quantified as a dose lethal to 50% of fish (LD50) for each host&ndash;isolate challenge. In the first set of experiments, 23 isolates were used to challenge groups of brook trout Salvelinus fontinalis. The mean LD50 was 1.087 x 10 6 colony-forming units per milliliter (cfu/mL; SD = 2.022 x 10 6 ), and the LD50 values ranged from 8.457 x 10 6 to 2.227 x 10 4 cfu/mL. Analysis of variance to evaluate the effect of isolate origin on virulence in brook trout revealed no significant difference ( F = 1.502; P = 0.243). Susceptibilities of the other salmonid hosts were evaluated by challenge with six isolates of R. salmoninarum representing each origin and the species type strain. For many of the host&ndash;isolate challenge combinations, time to death was highly dependent on the dilution (number of bacteria) injected. In general, the isolates MCO4M, B26, and A34 (all of Lake Michigan origin) tended to be more virulent. Also, LD50 values were dispersed throughout a wider range among the more susceptible hosts. Lake trout Salvelinus namaycush, rainbow trout Oncorhynchus mykiss, and brook trout were relatively resistant to challenge with the strains, whereas coho salmon O. kisutch, domestic Atlantic salmon Saltno salar, and chinook salmon O. tshawytscha were relatively susceptible. Another challenge evaluated the effect of washing R. salmoninarum MCO4M cells before injection into brook trout. The calculated LD50 value, 2.009 x 10 5 cfu/mL, was similar ( X 2 = 0.878; P = 0.645) to that of the unwashed cells (1.163 x 10 5 cfu/mL). Furthermore, times to death for successive dilutions were similar regardless of whether or not the cells were washed.

Journal of Aquatic Animal Health↗

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↗

Aquatic biological communities and associated habitats at selected sites in the Big Wood River Watershed, south-central Idaho, 2014

Assessments of streamflow (discharge) parameters, water quality, physical habitat, and biological communities were completed between May and September 2014 as part of a monitoring program in the Big Wood River watershed of south-central Idaho. The sampling was conducted by the U.S. Geological Survey in cooperation with Blaine County, Trout Unlimited, the Nature Conservancy, and the Wood River Land Trust to help identify the status of aquatic resources at selected locations in the watershed. Information in this report provides a basis with which to evaluate and monitor the long-term health of the Big Wood River and its major tributaries. Sampling sites were co-located with existing U.S. Geological Survey streamgaging stations: three on the main stem Big Wood River and four on the North Fork Big Wood River (North Fork), Warm Springs Creek (Warm Sp), Trail Creek (Trail Ck), and East Fork Big Wood River (East Fork) tributaries. The analytical results and quality-assurance information for water quality, physical habitat, and biological community samples collected at study sites during 2 weeks in September 2014 are summarized. Water-quality data include concentrations of major nutrients, suspended sediment, dissolved oxygen, and fecal-coliform bacteria. To assess the potential effects of nutrient enrichment on algal growth, concentrations of periphyton biomass (chlorophyll- a and ash free dry weight) in riffle habitats were determined at each site. Physical habitat parameters include stream channel morphology, habitat volume, instream structure, substrate composition, and riparian vegetative cover. Biological data include taxa richness, abundance, and stream-health indicator metrics for macroinvertebrate and fish communities. Statistical summaries of the water-quality, habitat, and biological data are provided along with discussion of how these findings relate to the health of aquatic resources in the Big Wood River watershed. Seasonal discharge patterns using statistical summaries of daily discharge from selected sites are reported for water years 2012–15. Results showed that annual average daily mean discharge increased from the Big Wood River near Ketchum, ID (BW Ketchum) downstream to the Big Wood River at Hailey, ID (BW Hailey), but decreased by nearly 50 percent from BW Hailey downstream to Big Wood River at Stanton Crossing near Bellevue, ID (BW Stanton). Annual variability in daily mean discharge among main-stem sites was highest at BW Stanton, suggesting that this part of the river may be subject to some level of flow alteration. Hydrologic alterations resulting in flow reduction can contribute to higher water temperature, especially during the summer months when conditions are often most stressful to fish and other stream organisms. Daily water temperature and water temperature trends from June to September 2014 are reported for select tributary and main-stem sites on the Big Wood River and can be used to assess the potential for biological impairment based on aquatic life temperature criteria for cold-water streams. The State of Idaho maximum temperature criteria for protection of cold-water aquatic life of 22 °C was exceeded at Warm Sp and BW Stanton during summer 2014, but at none of the other main-stem or tributary sites. The 13 °C critical temperature criterion for salmonid spawning was exceeded in early July 2014 at BW Ketchum and BW Hailey near the end of the rainbow trout critical spawning and rearing period. Temperature exceedances were most frequent at BW Stanton, where exceedances for rainbow trout and brown trout occurred from May through early July 2014 during most of the critical spawning and rearing period. Water quality and habitat availability did not seem to be limiting for fish or other aquatic organisms at most sites in the Big Wood River watershed. Water quality assessments in September 2014 determined no exceedances of total maximum daily load target levels. The availability and quality of habitat was limited at BW Stanton, where shallow-water habitat conditions prevailed. Macroinvertebrate community diversity was high at all sites except for BW Stanton, where low community diversity was attributed to low species richness and high abundances of a few tolerant taxa. Presence of low species diversity and high macroinvertebrate tolerance values at BW Stanton indicates that benthic community condition and stream health were reduced at that location. Fish surveys done in September 2014 did not indicate any significant reductions in native fish communities in the Big Wood River or its tributaries. Native rainbow trout ( Oncorhynchus mykiss ) and Wood River sculpin ( Cottus leiopomus ) were the dominant fish species in the drainage and were found at all tributary and main-stem sites. Non-native brown ( Salmo trutta ) and brook trout ( Salvelinus fontinalis ) were limited to lower drainage sites on the Big Wood River (BW Hailey and BW Stanton), and occurred in relatively low numbers.

Idaho↗