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Nicholas S. Voss

Publications and source records attributed to Nicholas S. Voss.

6 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

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

Reach-scale associations between introduced Brook Trout and juvenile and stream-resident Bull Trout in Idaho

Objective Native Bull Trout Salvelinus confluentus populations can be influenced by a variety of stressors operating at multiple spatial scales, making the relative importance of biotic versus abiotic controls difficult to discern at small scales where monitoring and management typically occur. Nonnative Brook Trout S. fontinalis were widely introduced throughout western North America and negatively affect Bull Trout occurrence. Here, we examine reach-scale associations between nonnative Brook Trout and juvenile and stream-resident Bull Trout (i.e., <250 mm) abundances through the lens of a constraining threshold, where nonnative fish exceeding a certain fish density may constrain native fish abundance. Methods We used a large spatial data set to define the abiotic conditions in which stream-dwelling Brook Trout and Bull Trout smaller than 250 mm typically co-occur in Idaho. Next, we queried multipass electrofishing survey data collected in reaches with abiotic conditions suitable for both species within localized areas where their distributions overlap. We then used two-dimensional Kolmogorov–Smirnov tests to identify threshold Brook Trout densities beyond which Bull Trout less than 250 mm were consistently rare or absent. Result Bull Trout smaller than 250 mm were rare or absent where Brook Trout density exceeded 0.54 fish/100 m 2 across the full range of abiotic conditions over which both species overlapped. However, Brook Trout rarely occurred in habitats associated with high Bull Trout density (e.g., where mean August water temperatures were 8.2°C). Conclusion Our results support existing hypotheses that the long-term co-occurrence of Bull Trout and Brook Trout in stream reaches suitable for both species may be unstable. Because low densities of Brook Trout appear to threaten Bull Trout, additional research is needed to better understand factors driving ongoing range shifts and invasion dynamics in Bull Trout habitat. We provide a simple tool to inform where Brook Trout represent a primary threat to Bull Trout, with potential applications for future monitoring, threat assessments, and conservation efforts.

Idaho

The importance of phenology and thermal exposure to early life history success of nonnative Smallmouth Bass in the Yellowstone River

Knowledge of potential spread by introduced species is critical to effective management and conservation. The Smallmouth Bass Micropterus dolomieu is an example of a fish that has been introduced globally, often spreads after introduction, and has substantial predatory impacts on fish assemblages. Nonnative Smallmouth Bass in the free-flowing Yellowstone River, Montana, have expanded from warmer, downstream sections of river into colder, upstream sections containing socio-economically valuable trout fisheries. We sought insight into mechanisms controlling upstream spread by evaluating whether progressively colder upstream climates physiologically constrained successful recruitment by limiting age-0 growth and preventing overwinter survival (i.e., population establishment). We documented the phenology, growth, and overwinter survival of age-0 Smallmouth Bass across a temperature gradient leading to their upstream extent in the Yellowstone River. The upstream extent of population establishment did not appear limited by water temperature alone. Age-0 body size at the onset of winter did not differ significantly between colder, upstream reaches and warmer, downstream reaches. Instead, the earlier hatch timing exhibited by some age-0 individuals in upstream sections allowed them to experience longer growing seasons than many individuals in downstream sections. This counter-intuitive hatching phenology mediated much of the expected decreases in growth in colder, upstream climates. Furthermore, evidence of successful overwinter survival and simulations of age-0 starvation mortality indicated that age-0 individuals at the upstream extent of their distribution successfully recruited to the age-1 year-class during four consecutive years. However, age-0 individuals were rare or absent throughout the uppermost upstream distribution of adults, suggesting that something other than temperature limits or discourages reproduction farther upstream. Taken together, our results suggest that Smallmouth Bass have not yet reached the thermal limit of their upstream distribution in the Yellowstone River and that future spread may challenge fisheries managers tasked with management of coldwater trout fisheries in this river.

Montana, Wyoming

Installation and performance of the Albuquerque Seismological Laboratory small-aperture posthole array

The Global Seismographic Network (GSN) has been used extensively by seismologists to characterize large earthquakes and image deep earth structure. Although the network’s original design goals have been met, the seismological community has suggested that the incorporation of small-aperture seismic arrays at select sites may improve performance of the network and enable new observations. As a pilot study for this concept, we have created a 500 m aperture, nine-element broadband seismic array around the GSN station ANMO (Albuquerque, New Mexico) at the U.S. Geological Survey Albuquerque Seismological Laboratory (ASL). The array was formed by supplementing the secondary borehole seismometer (90 m depth) at ANMO with eight additional 2.6 m posthole sites. Each station’s seismometer was oriented using a fiber optic gyroscope to within 2.0° of north. Data quality, particularly on the vertical components, is excellent with median power levels closely tracking the secondary sensor at ANMO at frequencies lower than 1 Hz. Horizontal component data are more variable at low frequencies (< 0:02 Hz), with the type of installation and local geography appearing to strongly influence the amount of tilt-induced noise. Throughout the article, we pose several fundamental questions related to the variability and precision of seismic wavefield measurements that we seek to address with data from this array. In addition, we calculate the array response and show a few examples of using the array to obtain back azimuths of a local event and a continuous narrowband noise source. The apparent velocity of the event across the array is then used to infer the local P-wave velocity at the ASL. Near real-time data collected from the array along with collocated meteorological, magnetic, and infrasound data are freely available in near-real time from the Incorporated Research Institutions for Seismology Data Management Center.

New Mexico