USGS ScienceSearch

Geology topics

Michael C. Quist

Publications and source records attributed to Michael C. Quist.

At least 19 recordsLinked to original sources

Patterns of recent brook trout invasion in bull trout streams in relation to habitat, source connectivity, biotic resistance, and disturbance

Knowledge of which habitats are at risk of invasion by nonnative species is essential to conservation, but a changing climate often complicates assessments of where future invasions may occur. Nonnative brook trout Salvelinus fontinalis threaten cold-adapted native salmonids throughout western North America, and the extent of future invasions in coldwater streams is recognized as an area of uncertainty with important consequences. We addressed this uncertainty using spatial-stream-network (SSN) modeling to develop a species distribution model (SDM) for brook trout in Idaho, creating high-resolution prediction maps of suitable (i.e., invadable) habitat under baseline (1990–2015) and future (2080s) climate scenarios, and querying predictions within natal bull trout S. confluentus habitat patches (stream–subwatershed scale) for each scenario. Results indicated that brook trout will experience a net loss of suitable habitat in Idaho, but a large increase of suitable habitat in cold streams. The total proportion of bull trout habitat invadable by brook trout increased from 0.33 during the baseline scenario to 0.44 during the future scenario—a result of upstream expansions of brook trout habitat that were partially offset by contractions in bull trout habitat. Changes in the proportion of invadable habitat varied widely among bull trout patches. Between scenarios, the largest increases in suitable habitat occurred in small, low-gradient, unconfined streams with mean August water temperatures of 7–9 °C during the baseline period. A relatively small proportion of patches contained the majority of invadable habitat in both scenarios, particularly patches in “U-shaped” glacial valleys. A changing climate will broadly increase the threat that brook trout pose to bull trout, but the degree of change experienced by individual populations will vary with local context. The high-resolution prediction maps created by our SSN model will help conservation planners identify and prioritize control efforts on the small proportion of brook trout populations that most threaten bull trout.

Idaho

Revised length categories and standard weight equation for Northern Pikeminnow

Objective Length and weight indices (e.g., proportional size distribution, relative weight) provide standardized benchmarks that are useful for comparing groups of fish, identifying ecological interactions, and evaluating the effect of management actions. However, the current length categories and standard weight ( W s ) equation for Northern Pikeminnow Ptychocheilus oregonensis , a species of important management focus in the Pacific Northwest, were developed using limited data, unclear methods, and no validation. As such, we sought to revise the length categories and W s equation for Northern Pikeminnow. Methods We used the all-tackle world record to develop length categories for Northern Pikeminnow. We compiled data from 100,663 Northern Pikeminnow from 114 populations in Idaho, Montana, Oregon, Washington, and British Columbia to develop a revised W s equation. Most fish were measured in fork length (FL), so we converted total lengths (TLs) to FLs using the equation TL = −2.301 + 0.916(FL); r 2 = 0.998. We used the regression line percentile, linear empirical percentile (EmP), and quadratic EmP methods to develop 50th percentile and 75th percentile W s equations. We then assessed length-related biases in our W s equations and the previously published equation. Results We propose minimum FLs of 17 cm (7 inches; stock), 26 cm (10 inches; quality), 35 cm (14 inches; preferred), 41 cm (16 inches; memorable), and 51 cm (20 inches; trophy) for proportional size distribution calculations. The previously published W s equation exhibited substantial length-related biases according to the Willis and weighted empirical quartile method tests. The EmP 50th-percentile W s equation was the only equation that we evaluated that did not exhibit length-related bias. The EmP 50th-percentile W s equation was the best performing equation (i.e., no length-related bias detected). The equation is log 10 ( W s ) = −5.258 + 3.135(FL), where W s is in grams and FL is in millimeters. The equation is valid for Northern Pikeminnow 90–580 mm FL. Conclusion The length categories, length conversion, and W s equation presented here will aid fisheries professionals in the study and management of Northern Pikeminnow populations.

British Columbia, Idaho, Montana, Oregon Washingto

Population and outmigration characteristics of juvenile Bull Trout in a montane ecosystem

Bull Trout Salvelinus confluentus is a federally threatened species in the conterminous United States. Although some populations are stable or increasing, Bull Trout in the United States Fish and Wildlife Service's designated Coeur d'Alene Core Area in Idaho have experienced substantial declines in abundance. Today, the remaining extant population in the Coeur d'Alene Core Area returns to the headwaters of the St. Joe River to spawn. The population has been monitored annually since 1992 using spawning ground surveys, but little is known about early life stages in the system. The objective of our research was to evaluate the distribution and abundance, age and size structure, habitat associations, and outmigration characteristics of juvenile Bull Trout in the upper St. Joe River basin. In 2022–2023, we sampled 200 stream reaches on the mainstem St. Joe River and four tributaries (Heller, Medicine, Sherlock, and Wisdom creeks). We sampled 1,529 Bull Trout varying in length from 29−257 mm in total length (TL; mean ± SD; 108 ± 44 mm). Population estimates suggested there were 1,841 (95% CI = 1,188−2,494) juvenile Bull Trout in the study area in 2022 and 2,388 (1,646−3,130) in 2023. Regression models indicated that abundance was positively related to canopy cover, amount of large substrate, amount of large woody debris, and amount of gravel, and negatively related to water temperature. We tagged 1,142 fish with passive integrated transponders (PIT) and detected 163 (14%) of these fish using a stationary tag array that was operational during June or July through October. Peak autumn outmigration occurred in October of both sampling years. Of the fish that were detected moving, age varied from 1−4 years, but age-1 and age-2 fish were more commonly detected moving downstream compared to other age classes. This study provides important information on the ecology of juvenile Bull Trout that can be used to guide conservation and recovery efforts in montane ecosystems. Furthermore, juvenile Bull Trout in the upper St. Joe River basin were present at similar densities and experienced growth rates similar to more robust adfluvial populations (e.g., Lake Pend Oreille, Idaho), thereby indicating that factors contributing to the low abundance of adults are not likely occurring in the headwaters of the St. Joe River. Thus, conservation efforts may be more successful if they are focused on the migration corridor and Coeur d'Alene Lake.

Idaho

Population structure and movement dynamics of Redband Trout in the Kootenai River basin

Redband Trout Oncorhynchus mykiss gairdneri is a species of high conservation concern in the Kootenai River basin, United States and Canada. However, identifying the specific mechanisms influencing Redband Trout is difficult as its life history structure is largely unknown. Using otolith microchemistry analysis, we found that 18.5% ( n = 66) of the fish sampled ( n = 329) were a product of mainstem Kootenai River spawning. The remainder were fish ( n = 264) that originated from one of 31 tributaries throughout the basin. Redband Trout were captured between 0 and 153 km from their assigned natal tributaries. Most migratory fish originated from tributaries in the uppermost portion of the study area and had migratory mothers. However, a diversity of life history types (e.g., multi-year resident, migratory) was observed in the population. Redband Trout were estimated to outmigrate from natal habitats at a variety of ages (0–3 years) and lengths (12–430 mm). Our results highlight diversity in the population structure of Redband Trout and provide information valuable to conservation efforts in the Kootenai River system. Interestingly, several tributaries identified as natal habitats of Redband Trout contain substantial obstacles originally considered barriers to upstream fish passage. In addition, some streams in the lower portion of the Kootenai River basin with degraded habitat that were not expected to contribute Redband Trout had natal assignments. These observations indicate previously unknown sources of Redband Trout and support the notion that improved fish passage in disconnected and degraded streams could increase production of Redband Trout throughout the Kootenai River basin. Restoration efforts in the mainstem that include considerations for spawning and natal habitat may also aid in conservation efforts for Redband Trout. Our research demonstrates the value of microchemistry in planning and evaluating habitat restoration to recover fishes in large rivers.

British Columbia, Idaho, Montana

Food habits of nonnative Smallmouth Bass in Coeur d’Alene Lake, Idaho

Smallmouth Bass ( Micropterus dolomieu ) has been widely introduced beyond its native distribution where interactions with other organisms are largely unknown. We examined the food habits of Smallmouth Bass in Coeur d'Alene Lake, Idaho. Smallmouth Bass were sampled monthly from March 2012 to May 2013 using short duration (1–2 hr sets) gill netting and electrofishing. In total, food habits were evaluated from 904 Smallmouth Bass varying in total length from 39 to 492 mm using gastric lavage. Diet composition varied by season and age. Smallmouth Bass less than 100 mm had diets dominated by invertebrates, particularly Ephemeroptera, Odonata, and Diptera. Fishes were increasingly important in the diet of Smallmouth Bass longer than 100 mm. Interestingly, crayfish (Decapoda) were virtually absent in Smallmouth Bass stomachs; only eight Smallmouth Bass had crayfish in their diet. Native vertebrates were also rare in Smallmouth Bass diets. Rather, kokanee ( Oncorhynchus nerka ), a nonnative species, was generally the most commonly consumed fish prey item (present in 5–15% of Smallmouth Bass across seasons). Kokanee contributed the highest percentage of total energy (approximately 45% of all energy) of any prey item. Results of this study suggest that native fishes of conservation concern are a minor component of Smallmouth Bass diets and that kokanee is important in meeting the energy demands of nonnative Smallmouth Bass. Further research on the distribution and abundance of crayfish in the system and on the population-level effects of Smallmouth Bass predation on kokanee would be insightful and help guide management actions in Coeur d'Alene Lake and similar systems in western North America.

Idaho

Food habits of Yellow Perch, Smallmouth Bass, and Northern Pikeminnow in Lake Cascade, Idaho

Objective Yellow Perch Perca flavescens was first encountered in Lake Cascade, Idaho, in 1957. Since its introduction, the abundance of Yellow Perch in Lake Cascade has been highly variable. Historically, declines in Yellow Perch abundance were attributed to predation by Northern Pikeminnow Ptychocheilus oregonensis . In the 1990s, Smallmouth Bass Micropterus dolomieu became established in Lake Cascade. Although Yellow Perch abundance has been high and currently supports a world-class fishery, the Idaho Department of Fish and Game has documented poor Yellow Perch recruitment in recent years, concerning regional managers. An investigation into the food habits of Yellow Perch, Smallmouth Bass, and Northern Pikeminnow was conducted to better understand the importance of juvenile Yellow Perch to predator diets. Methods In Lake Cascade, gill nets were deployed monthly from April 2022 to May 2023. Ageing structures and stomach contents were removed from Yellow Perch, Smallmouth Bass, and Northern Pikeminnow. Diet composition was quantified and then summarized by species, cohort, and season. Bioenergetics modeling, coupled with estimates of predator abundance, was used to evaluate overall consumption of Yellow Perch. Results In total, stomach contents were extracted from 1,099 Yellow Perch, 440 Smallmouth Bass, and 980 Northern Pikeminnow. Food habits varied by season and predator length, but Yellow Perch was a primary prey item of all study species. The energetic contribution of Yellow Perch to Yellow Perch varied from 10% to 80% across seasons. Smallmouth Bass consumed fewer Yellow Perch than either Yellow Perch or Northern Pikeminnow. The highest average per capita consumption of Yellow Perch (i.e., across seasons) was observed for 500–600-mm Northern Pikeminnow (five Yellow Perch/Northern Pikeminnow). Energetic contribution of Yellow Perch to Northern Pikeminnow diets was highest in spring 2023, yet Northern Pikeminnow consumed the highest average number of Yellow Perch in July. Bioenergetics modeling estimated that per-capita annual consumption of Yellow Perch was 6.0 kg for Yellow Perch, 3.4 kg for Smallmouth Bass, and 9.9 kg for Northern Pikeminnow. In total, estimated consumption of all study species was as high as 37% of the estimated total number age-0 Yellow Perch produced. Conclusions Yellow Perch was an important prey item for all three species, particularly Yellow Perch and Northern Pikeminnow. Results from this study provide important information on the predation of Yellow Perch in Lake Cascade. Further, this work will bolster a growing body of research on the food habits of and interactions between native and nonnative predators in western reservoir systems.

Idaho

Population dynamics of White Sturgeon in the upper Snake River, Idaho: Evaluation of management options for a harvest fishery

Objective Understanding how fish populations will respond to management actions is critical for making effective management ­decisions. This study provides important information regarding population demographics for a nonnative, hatchery-implemented population of White Sturgeon Acipenser transmontanus . We investigated the population dynamics of White Sturgeon in the upper Snake River, Idaho, and developed an age-structured population model to evaluate potential stocking and harvest scenarios (e.g., length limits and annual quotas). Methods White Sturgeon were sampled from June to October 2022 and from June to August 2023 using angling (i.e., rod and reel) and setlines from a 260-km-long section of the Snake River. Capture histories from 261 known-age White Sturgeon informed age and growth analysis and an evaluation of movement trends. A closed-population capture–recapture model and an estimate of setline-specific catchability were used to estimate the total abundance of White Sturgeon in the upper Snake River. Apparent survival for the population was estimated using a Cormack–Jolly–Seber model. Finally, a population model was parameterized using information on the population dynamics of White Sturgeon in the upper Snake River. The model was used to estimate the effects of varying stocking rates and harvest scenarios (i.e., harvest slot of 76–122 cm fork length [FL] and annual quotas of 0–25 White Sturgeon harvested) on the population. Results In total, 340 individual White Sturgeon were captured throughout the study area, with 181 recapture events. Individuals varied in FL from 54 to 205 cm, and the mean relative weight for captures was 105.2 (SD = 14.4), suggesting relatively high body condition. Age varied from 2 to 25 years, and White Sturgeon moved an average of 8.1 km (SD = 23.5) downstream from stocking locations. Estimated abundance of White Sturgeon in the tailwaters of American Falls Dam was 428 fish (95% CI = 403–463). That abundance estimate was used to inform a total abundance estimate of 887 White Sturgeon (95% CI = 835–960) in the study area. Apparent annual survival was 0.79 (95% CI = 0.64–0.89). A stocking rate of 285 age-2 White Sturgeon/year was necessary to maintain current abundance. For every five fish harvested (harvest slot = 76–122 cm FL) per year, estimated abundance decreased by about 2.2% over 20 years. Conclusions Our research identified fast growth of White Sturgeon relative to other populations and relatively high mortality for a White Sturgeon population without exploitation. Also, like other studies evaluating harvest, a population model was used to illustrate the effect of varying rate functions on a fishery. The age-structured population model suggested that a harvest fishery is possible while still meeting management goals for the upper Snake River White Sturgeon fishery.

Idaho

Long-term patterns in growth of White Sturgeon in the Sacramento-San Joaquin River basin, California.

Introduction: The Sacramento-San Joaquin River system (SSJ) of California includes both riverine, delta, and estuarine habitats and is among the most modified aquatic ecosystems in the United States. Water development projects in the system are associated with declines of many native species, including White Sturgeon Acipenser transmontanus . Methods: We used White Sturgeon pectoral fin rays collected from 1983 to 2016 throughout the SSJ to assess long-term changes in growth and associations with thermal and hydrological conditions (i.e., temperature, discharge, salinity). Age and growth were estimated from 1,897 White Sturgeon varying in fork length from 25 to 210 cm and from age 0 to 33. Results: Age structure varied through time with the oldest fish generally sampled during the mid-1980s. Growth of White Sturgeon in 1951–1970 was slower than growth of fish in 1971–1990 and 1991–2012. Growth of White Sturgeon during 1991–2012 was ~10% higher than during other time periods. Discussion: Little variation in growth was explained by environmental covariates, suggesting that annual growth was likely influenced by factors not measured in our study. Alternatively, population structure and movement behavior of White Sturgeon in the SSJ may be such that the scale (i.e., spatial or temporal) of available habitat covariates was mismatched to the scale at which growth of White Sturgeon responds. Increased growth in recent times may be partly due to density-dependent processes in association with substantial declines in White Sturgeon population abundance over the last several decades. This research provides important information on long-term patterns in growth that contributes to the conservation and management of White Sturgeon in the SSJ and beyond.

California

Why the whole is greater than the sum of its parts: A case for population-level management

Catch-and-release regulations in recreational fisheries have been implemented for decades with the intention of allowing fishing while reducing fishing mortality. In addition, voluntary catch-and-release behaviors are increasingly common. Social and scientific interest in fish handling practices in catch-and-release fisheries as they relate to stress, reflex impairment, reproductive success, and mortality has been expanding. The scientific literature is now replete with studies that examine these issues, and they have become a fixture in the public discourse on angling. Scientists and anglers are making fishing regulation proposals and suggestions for fish-handling practices. The proximal intent of these recommendations is to reduce excessive stress or mortality on a per capita basis with a belief that the reduction ultimately has a positive effect on the population. Whether the proximal intent achieves population goals depends on several factors, including effort, population dynamic rates, and stock-recruitment dynamics. This perspective reviews the state of the science relative to a hierarchical framework of fishery population dynamics, with a call for fishery scientists to consider their scope of inference and assumptions relative to conservation and population management.

Article

Points of consensus on catch-and-release: Considerations for science, ethics, and fisheries management

Catch-and-release (C&R), whether via regulations or voluntary actions, is typically employed with the intent of reducing ­fishing mortality while maintaining recreational angling opportunities (Isermann & Paukert, 2010), but there has been significant discourse about the relative importance of individual-level (see Cooke et al., 2025) vs. population-level (see Corsi et al., 2025) effects of C&R. We hope to offer the angling, scientific, and management communities some points of consensus from which this multifaceted dialogue on C&R can productively build. We preface this by noting that our collective views were informed by this process and the opportunity to share and learn from each other. What is apparent from this exercise is the value of embracing a holistic, cooperative approach. From a regulatory perspective, C&R is typically implemented in high-effort fisheries that are popular due to the quality of the fishing. Catch-and-release regulations are also applied in fisheries where populations have declined and fishing mortality is thought or, most appropriately, known to be a limiting factor for the population. When practiced voluntarily, anglers engaging in C&R can be characterized by high avidity and specialization, and angling is often a central component of their identity (e.g., Fisher, 1997). Due to their passion, avid anglers tend to spotlight the ethical, scientific, and regulatory considerations of C&R. As such, there is a need in fisheries management and science to understand in what situations these considerations transcend biological scales and how to navigate the gamut of voluntary actions and regulatory mandates. In this essay, we offer a distillation of the emergent consensus concepts that we hope managers and researchers will consider at both individual and population scales for legal, ethical, and scientific deliberations.

Fisheries

Comparison of lapilli otoliths and pectoral fin rays for estimating age of Northern Pikeminnows

The Northern Pikeminnow Ptychocheilus oregonensis is a piscivorous cyprinid native to western North America. Information on the best structure for estimating the age of Northern Pikeminnows is a key knowledge gap that may limit inquiries on management efforts. Thus, the objective of this study was to evaluate between-reader precision and concordance between age estimates for lapilli otoliths and pectoral fin rays from Northern Pikeminnows. Age estimates from lapilli otoliths were compared to those from pectoral fin rays of 150 Northern Pikeminnows captured from Lake Cascade, Idaho, in April–May 2022. Exact percent agreement of estimated ages between the readers was higher for fin rays (75.3%) than otoliths (50.0%), with a mean coefficient of variation of 3.5 and 8.7, respectively. Readers also assigned a confidence rating (0–3; higher value reflects higher confidence in age estimate) to each structure. Confidence ratings were higher for fin ray age estimates (mean ± SD; 1.6 ± 0.6) than otolith estimates (1.1 ± 0.7) between readers. A consensus age was estimated for each structure and fish. Agreement between consensus age estimates for otoliths and fin rays was 26.7% with a coefficient of variation of 14.0. Our findings suggest that fin rays were easier to collect, process, and read than otoliths, and resulted in more precise age estimates than otoliths. Results from our study provide guidance on the best structures for estimating the age of Northern Pikeminnows that can be used to inform management efforts.

Idaho

Food habits of nonnative Walleyes in Lake Pend Oreille, Idaho

Objective Walleye Sander vitreus is an important species that has been widely introduced outside of its native distribution. The goal of this study was to assess the effects of an established Walleye population in the Lake Pend Oreille (LPO) system, Idaho. Methods Food habits of Walleyes were described using stomach contents and stable isotopes (δ 15 N, δ 13 C). Trophic structure of the LPO system's food web was identified using stable isotopes. Annual consumption by Walleyes of important prey items was estimated using a bioenergetics model. Result Walleyes consumed a diversity of prey items, including macroinvertebrates and fishes. Kokanee Oncorhynchus nerka , the most frequently consumed prey item, occurred in 23% of all Walleye diets. Combined, native cyprinids and catostomids occurred in 31% of all Walleye stomachs. Select taxa (e.g., native cyprinids, kokanee) were consistently consumed by Walleyes across seasons, regions, and cohorts, whereas other taxa (e.g., Westslope Cutthroat Trout O. lewisi , Smallmouth Bass Micropterus dolomieu ) were consumed inconsistently. Stable isotope analysis suggested that Walleyes occupied similar trophic positions as other top‐level piscivores in the system . As Walleye age increased, δ 15 N increased and δ 13 C decreased, indicating increased consumption of pelagic prey resources and prey at higher trophic positions. The estimated biomass of kokanee consumed annually by Walleyes was 27,121 kg (95% confidence interval = 9178–61,603). Comparatively, native cyprinids represented about 46% of the total biomass of kokanee consumed by Walleyes, whereas native catostomids represented about 11% and native salmonids represented about 15% of the total biomass of kokanee consumed by Walleyes. Conclusion This study revealed that Walleyes consumed various fishes across the LPO system. Although kokanee were the most frequently consumed prey item, native cyprinids and catostomids (combined) occurred at similar proportions. This study contributes to our growing knowledge of the effects of nonnative Walleyes on important salmonids and native fishes in western systems.

Idaho

Abiotic and biotic factors related to growth of non-native Walleyes in Lake Pend Oreille, Idaho

Objective Growth is one of the primary drivers of fish population dynamics and understanding factors influencing growth is vital to effective management of fish populations. This study investigated potential factors influencing growth of a recently established, non-native population of Walleye Sander vitreus in the Lake Pend Oreille system in northern Idaho. Methods We used relative growth index to describe growth of Walleyes relative to populations across North America. Mixed‐effects modeling was used to relate growth to abiotic (i.e., mean summer water temperature, river inflow) and biotic (i.e., kokanee Oncorhynchus nerka abundance and biomass; opossum shrimp Mysis diluviana density) variables. Models were ranked using Akaike's information criterion corrected for small sample size. Individual variability in growth was related to diet represented by stable isotopes (i.e., δ 15 N, δ 13 C) using linear regression for age‐1, age‐2, age‐3, and age‐5 individuals. Subsequently, for each age‐class, we evaluated differences in δ 15 N and δ 13 C between fast‐growing (i.e., 75th and higher percentiles of growth) and slow‐growing (i.e., 25th and lower percentiles of growth) individuals. Results The relative growth index suggested that Walleye grew fast relative to other populations, particularly those at similar latitudes to the Lake Pend Oreille system. Mixed-effects regression modeling indicated that growth of Walleyes was positively associated with temperature as well as abundance and biomass of kokanee; growth was negatively associated with inflow from the Clark Fork River and Mysis diluviana density. The top model explaining growth of Walleyes contained temperature and abundance of kokanee as environmental variables. The second equally plausible (i.e., within 2 AICc) model contained temperature. Growth of Walleyes varied among individuals. Generally, fast-growing Walleyes had higher δ15N than slow-growing Walleyes. Similarly, δ13C was more depleted in the fast-growing individuals for all age classes, except age 1, suggesting that age-1 individuals used higher proportions of littoral prey items compared to other age classes. Conclusion This study showed that kokanee abundance and temperature appeared to be important factors influencing growth of Walleyes in the Lake Pend Oreille system. Additionally, variability in growth appeared to be related to variability in diet, particularly for age-1 Walleyes. Impact statement Growth of Walleyes has been extensively studied, yet few studies have evaluated growth of Walleyes in novel systems or assessed individual variability in growth. Our research adds to the understanding of individual variability in growth and factors influencing population dynamics of non-native Walleyes.

Idaho

Retention of T‐bar anchor tags by adult steelhead during their upstream migration

Objective: T-bar anchor tags can be used to obtain recapture data from anglers, directly estimate exploitation, and evaluate population dynamics. Unfortunately, their use by biologists to study anadromous salmonid fisheries is limited. Two hurdles to adoption include the functional difficulty of tagging large anadromous salmonids using conventional tagging equipment and a lack of information on tag loss by large anadromous salmonids and how it changes over time. As such, our objectives were to (1) describe a T-bar anchor tagging system modified to study adult steelhead Oncorhynchus mykiss (i.e., anadromous Rainbow Trout) and (2) present an instantaneous tag loss model for steelhead that allows estimation of tag loss over time. Methods: First, we developed a modified tagging system by tagging hatchery-obtained steelhead carcasses and live, resident Rainbow Trout >500 mm using a variety of hardware and tag dimensions. Next, we double-tagged adult steelhead captured at the Lower Granite Dam adult fish trap, Washington, USA. We then used data from 182 recaptured steelhead to fit an instantaneous tag loss model. Last, we investigated whether steelhead tag loss was related to body length. Result: Tag loss was generally low within the time period under study (i.e., up to 221 days between release and recapture). The estimated probability of tag loss was 0.034 at release, 0.044 at one month, and 0.113 at eight months. We failed to detect significant differences in tag loss parameters between two subsets of small (<720 mm) and large (≥720 mm) steelhead. Conclusion: T-bar anchor tags are useful external tags for studying adult steelhead during their upstream migration. Because anglers can be used to provide recapture data, T-bar anchor tags may be particularly useful where angler effort is high or direct estimation of fishery exploitation is desired.

Washington

Nonnative Smallmouth Bass in the Snake River, Idaho: Population dynamics, demographics, and management options

The Snake River in Idaho, USA, supports a popular sport fishery for nonnative Smallmouth Bass Micropterus dolomieu , but there are limited studies on the population dynamics of this introduced species in Idaho and other water systems in the western United States. The purpose of this study was to describe the population dynamics and demographics of Smallmouth Bass in the Snake River, Idaho. In total, we sampled 4,929 Smallmouth Bass during electrofishing surveys on the Snake River (separated into nine segments) and three major tributaries (Boise, Payette, and Weiser rivers). We estimated age for 1,869 Smallmouth Bass sampled from the Snake River ( n = 1,433) and three tributaries ( n = 436). Catch-per-unit-effort for all nine segments combined on the Snake River was 36.6 fish/h (±4.4 SE). In the tributaries, catch-per-unit-effort varied from 43.6 to 125.0 fish/h. Relative weight of all Smallmouth Bass varied from 86 to 107, indicating that fish were in relatively good body condition. Fish in the system grew fast, with relative growth index values often near or exceeding 100 for all age classes. Total annual mortality for the Snake River was 45.1 ± 0.7%, and it was 36.8–40.5% in the tributaries. Furthermore, we estimated exploitation to be 5.3% (90% CI; ±2.2%) for the Snake River and tributaries combined. We used a yield-per-recruit population model to evaluate the effects of varying minimum length limits on the fishery. With the observed population demographics and exploitation rates, increasing the current minimum length limit from 305 mm to 356 or 406 mm would probably have little influence on the number of Smallmouth Bass available to anglers. However, increasing the length limit would result in reduced biomass available for harvest. The potential for recruitment overfishing was minimal for all minimum length limits and levels of exploitation. As such, changes to current harvest regulations do not appear warranted. Our findings provide important information on the population dynamics of Smallmouth Bass that can be useful in evaluating their management across Idaho and in similar systems in western North America.

Idaho

An evaluation of fin ray microchemistry to describe movement of White Sturgeon in the Kootenai River basin: Insights and limitations

Introduction: White Sturgeon Acipenser transmontanus in the Kootenai River basin is listed as endangered in the United States and Canada. Declines have been mainly attributed to poor recruitment exacerbated by the environmental effects of Libby Dam in Montana. Reduced primary production downstream of Libby Dam has been identified as one factor limiting growth of White Sturgeon, thereby limiting natural reproduction through delayed sexual maturity. However, estimating changes in growth over time without knowledge of fish location (i.e., Kootenai River vs. Kootenay Lake) is difficult. The objective of this project was to use microchemistry analysis to describe the movement of White Sturgeon within the Kootenai River basin. Methods: Water samples ( n = 27) and White Sturgeon fin rays ( n = 162) collected in the Kootenai River basin were measured for strontium isotope ( 87 Sr: 86 Sr) ratios using laser ablation multicollector inductively coupled plasma mass spectrometry. All water samples and a subset of fin rays ( n = 8) were also analyzed for trace elements (e.g., Sr, Ba, Mg). Fin ray annuli were measured and tested using knowledge of known age; known locations from physical capture events were assigned to age at capture. Results: Strontium isotope analysis was unable to detect differences in the Kootenai River and Kootenay Lake using water or fin ray samples. The Kootenai River and Kootenay Lake were distinguishable using trace element data from water samples, but not fin rays. The discrepancy with trace elements appears to be associated with the physiology of fin ray growth. Discussion: Although this study did not meet its original objective of describing the movement of White Sturgeon in the Kootenai River basin from fin ray microchemistry, our results provide insight into the potential influence of physiology on microchemistry analysis. In particular, fin ray microchemistry of slow-growing fishes may be possible in freshwater systems with further investigation into the physiological processes associated with growth and the incorporation of elements into calcified structures.

British Columbia, Idaho, Montana

Evaluation of techniques for estimating the age and growth of known‐age White Sturgeon

Objective Successful conservation and management of fishes require an understanding of their age and growth. However, methods for estimating the age and growth of long-lived fish species are difficult to validate. The Kootenai River basin has a decades-long mark–recapture program for endangered White Sturgeon Acipenser transmontanus . The mark–recapture history information for White Sturgeon allowed for the evaluation of fin rays for age and growth analysis. Methods Age was estimated from pectoral fin rays of known‐age White Sturgeon ( n = 162) to evaluate ageing accuracy and precision. Lengths were back‐calculated using four models and measurements obtained from two fin ray transects (i.e., lateral and posterior). Result Between-reader agreement for White Sturgeon ages was 58.7%. Consensus age agreement with known ages was poor (30.7%) and decreased with age. Among the four back-calculation models, the Fraser–Lee model provided the lowest root mean square error and percent error. Estimates of mean back-calculated lengths at age derived from the Fraser–Lee model were similar between the two measurement transects. Back-calculated lengths at age were similar to known lengths at age. Conclusion Ageing of White Sturgeon using fin rays was unreliable, and accuracy decreased with fish age. Back-calculated lengths at age were accurate using measurements from fin rays of known-age fish. Length estimates from the two measurement transects were similar when using the Fraser–Lee method, suggesting that they may be used interchangeably.

Idaho, Montana

Leveraging angler effort to inform fisheries management: Using harvest and harvest rate to estimate abundance of White Sturgeon

Traditional methods for estimating abundance of fish populations are not feasible in some systems due to complex population structure and constraints on sampling effort. Lincoln’s estimator provides a technique that uses harvest and harvest rate to estimate abundance. Using angler catch data allows assumptions of the estimator to be addressed without relying on methods that could be prohibitively field-intensive or costly. Historic estimates of White Sturgeon Acipenser transmontanus abundance in the Sacramento–San Joaquin River basin have been obtained using mark–recapture methods; however, White Sturgeon population characteristics often cause violations of model assumptions, such as population closure and independent capture probabilities. We developed a version of Lincoln’s estimator using a joint likelihood, estimated abundance of White Sturgeon in the Sacramento–San Joaquin River basin in 2015 using this method and empirical data and assessed accuracy and precision of estimates in a simulation study. Estimating abundance using harvest and harvest rate, as represented by our model framework, has the potential to be precise and accurate. The joint likelihood–based approach fitted using Bayesian methods is advantageous because it includes all sources of variation in a single model. Precision of abundance estimates was low with application of the model to White Sturgeon in the Sacramento–San Joaquin River basin and to similar conditions in a simulated dataset. Using simulation, precision and accuracy increased with increases in the number of high-reward and standard tags released, tag reporting rate, tag retention rate, and harvest rate. Results demonstrate potential sources of error when using this approach and suggest that increasing the number of tagged fish and tag reporting rate are potential actions to improve precision and accuracy of abundance estimates of the model.

California