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Tower counts

Counting towers provide an accurate, low-cost, low-maintenance, low-technology, and easily mobilized escapement estimation program compared to other methods (e.g., weirs, hydroacoustics, mark-recapture, and aerial surveys) (Thompson 1962; Siebel 1967; Cousens et al. 1982; Symons and Waldichuk 1984; Anderson 2000; Alaska Department of Fish and Game 2003). Counting tower data has been found to be consistent with that of digital video counts (Edwards 2005). Counting towers do not interfere with natural fish migration patterns, nor are fish handled or stressed; however, their use is generally limited to clear rivers that meet specific site selection criteria. The data provided by counting tower sampling allow fishery managers to determine reproductive population size, estimate total return (escapement + catch) and its uncertainty, evaluate population productivity and trends, set harvest rates, determine spawning escapement goals, and forecast future returns (Alaska Department of Fish and Game 1974-2000 and 1975-2004). The number of spawning fish is determined by subtracting subsistence, sport-caught fish, and prespawn mortality from the total estimated escapement. The methods outlined in this protocol for tower counts can be used to provide reasonable estimates ( plus or minus 6%-10%) of reproductive salmon population size and run timing in clear rivers.

Book chapter↗

Age and growth of the whitefish in Lake Superior

The average annual commercial production of whitefish in the U.S. waters of Lake Superior dropped from 2,194,000 pounds in 1879-1908 to 504,000 pounds in 1911-59. The modern production, though far below the earlier, has accounted for more than 10 percent of the total value of the fishery in all but one of the last 20 years. Data are given on growth rate, age and year-class composition, size distribution, and length-weight relation of 1,800 fish collected in 1957-59 at Bayfield, Wis., and Marquette, Whitefish Point, and Dollar Settlement, Mich. Studies of the body-scale relation, sex ratio, and age and size at maturity were limited to fish collected at Bayfield. The age composition and mean age varied widely by port and year of capture. Oldest fish were those of the 1957 Bayfield samples which were dominated by age group VII and averaged 5.5 years old. The youngest were from Whitefish Point in 1959; age-group III was dominant, and the mean age was 3.2 years. The evidence on the strength of year classes was not clear-cut, but it was obvious that fluctuations in stocks of different areas were largely independent. The percentage of legal-size fish (17 inches or longer) in age groups ranged widely; only 8.6 percent of the V group were legal in the 1957 Bayfield collections, whereas 100 percent of fish of the same age were legal in the 1957-59 collections from Whitefish Point. The weight of whitefish in the combined samples increased as the 3.2408 power of the length. The growth rate from the fastest to the slowest growing stocks ranked as follows: Whitefish Point; Dollar Settlement and Marquette (fish from the two ports reversed ranks after 3 years); Bayfield. The major differences in growth in length among the various stocks occurred during the first years of life. Beyond the fifth year the annual increments were nearly the same in all stocks. The whitefish from Whitefish Point, Dollar Settlement, and Marquette are among the fastest growing in the Great Lakes. The differences among the Lake Superior stocks in age and year-class composition, and in growth rate offer convincing evidence that populations of different areas are entirely independent. The sexes were almost equally represented (51.5 percent males) in the combined Bayfield samples, but males were scarce in age groups older than VIII. Whitefish from Bayfield shorter than 14.5 inches were immature and those larger than 17.4 inches were mature. The youngest mature fish belonged to age-group V,and all older than the VII group were mature.

Fishery Bulletin↗

Catch rates relative to angler party size with implications for monitoring angler success

Angler catch rates often are used to monitor angler success, assess the need for additional management actions, and evaluate the effectiveness of management practices. Potential linkages between catch rate and angler party size were examined to assess how party size might affect the use of catch rate as an index of angler success in recreational fisheries. Data representing 22,355 completed interviews conducted at access points in lakes and reservoirs throughout Mississippi during 1987-2003 were analyzed. Total party catch was not proportional to total party effort; thus, catch rate decreased as party size increased. Depending on the taxa targeted, the average catch rate per angler decreased 40-50% between parties of one and parties of two, although subsequent decreases were less substantial. Because party size accounted for a considerable portion of the variability in catch rate over time and space, failure to remove this variability weakens the manager's ability to detect differences or changes in catch rates. Therefore, the use of catch rates to monitor fisheries may be inappropriate unless party size is taken into account. Party size may influence the angler's ability to catch fish through a variety of processes, including partitioning a limited number of catchable fish among members of a party and party composition. When catch rates are used to estimate total catch rather than to index angler success, party size is not a concern.

Transactions of the American Fisheries Society↗

Migratory behavior of Chinook salmon microjacks reared in artificial and natural environments

Emigration was evaluated for hatchery Chinook salmon ( Oncorhynchus tshawytscha ) microjacks (age-1 mature males) and immature parr (age-1 juveniles, both sexes) released from both a hatchery and a natural stream (fish released as fry). In the hatchery, volitional releases (&sim;14 to 15 months post-fertilization) to an adjacent river occurred during October&ndash;November. The hatchery release was monitored by using an experimental volitional release that diverted fish to a neighboring raceway. Fish captured during the experimental release (range 361&ndash;4,321 volitional migrants) were made up of microjacks and immature parr. Microjacks were found only in the migrant samples, averaged 18% (range 0&ndash;52%) of all migrants, and were rarely found in non-migrant samples. In comparison, immature parr were common in both the migrant and non-migrant samples. Microjacks were significantly longer (9%), heavier (36%), and had a greater condition factor (16%) than migrant immature parr (P<0.01). In addition, they differed significantly (P<0.01) from non-migrant immature parr; 10% longer, 44% heavier and 14% greater condition factor. In natural streams, microjacks were captured significantly earlier (P<0.01) than immature parr during the late-summer/fall migration and comprised 9&ndash;89% of all fish captured. Microjacks have the potential to contribute to natural spawning populations but can also represent a loss of productivity to hatchery programs or create negative effects by introducing non-native genes to wild populations and should be monitored by fishery managers.

Journal of Fish and Wildlife Management↗

A comparison of age- and size-structured assessment models applied to a stock of cisco in Thunder Bay, Ontario

Stock assessments are critical to modern fisheries management, supporting the calculation of key reference variables used to make informed management decisions. However, there is still considerable uncertainty as to which class of assessment models is appropriate to use under different circumstances. A common class of models used when age data are available are statistical catch-at-age assessment (SCAA) models, which track annual cohorts through time. When age data are unavailable, as is often the case in invertebrate fisheries where the lack of a bony structure such as otoliths makes aging difficult, statistical catch-at-size assessment (SCSA) models are more often employed, tracking fish or invertebrates through time by size-classes rather than ages. Do SCAA models actually perform better than SCSA models when age data are available, or is this just an assumption we make in fisheries research and management? We examined this question by evaluating the effectiveness of both SCAA and SCSA models in characterizing cisco, Coregonus artedi , population dynamics in Thunder Bay, Ontario. Both models were fit using an integrated framework with multiple sources of data including hydroacoustic estimates of spawning stock, fishery-dependent and -independent age/length compositions, and harvest data. Our results suggest that for cisco in Thunder Bay, data-limitations related to lack of size-composition data over the size range for which cisco growth is rapid resulted in difficulty estimating relative year-class strength within a SCSA. This led to parameter confounding and ultimately the inability to estimate natural mortality within a SCSA. This hampered the utility of a SCSA model in comparison with a SCAA model when age-composition data were available.

Ontario↗

Constraints of body size and swimming velocity on the ability of juvenile rainbow trout to endure periods without food

The hypothesis that body size and swimming velocity affect proximate body composition, wet mass and size-selective mortality of fasted fish was evaluated using small (107 mm mean total length, LT) and medium (168 mm mean LT) juvenile rainbow trout Oncorhynchus mykiss that were sedentary or swimming (c. 1 or 2 body lengths-1) and fasted for 147 days. The initial amount of energy reserves in the bodies of fish varied with L T. Initially having less lipid mass and relatively higher mass-specific metabolic rates caused small rainbow trout that were sedentary to die of starvation sooner and more frequently than medium-length fish that were sedentary. Swimming at 2 body length s-1 slightly increased the rate of lipid catabolism relative to 1 body length s-1, but did not increase the occurrence of mortality among medium fish. Death from starvation occurred when fish had <3.2% lipid remaining in their bodies. Juvenile rainbow trout endured long periods without food, but their ability to resist death from starvation was limited by their length and initial lipid reserves. ?? 2004 The Fisheries Society of the British Isles.

Journal of Fish Biology↗

Historical changes in the major fish resources of the Great Lakes

My purpose here is to review historic changes in the major fish resources of the five Great Lakes, and to identify the cause or causes for those changes. In some instances it will be clear that intensive fishing was the primary cause of change; in other instances it will be nearly as clear that predation by the sea lamprey played a significant if not dominant role in change; and in still others it will be clear (or at least circumstantial) that exotic species other than the sea lamprey have been implicated. The exotics that have invaded or been accidentally or purposefully released into the Great Lakes system have not only adversely affected indigenous fishes, but some have developed into new and valuable resources. However, when it comes to degradation of water quality and of critical habitat, the linkages to changes in fish populations are neither clear-cut nor quantifiable — their impacts were generally far more subtle and difficult to detect, but not necessarily of less importance. Inasmuch as a comprehensive review of all changes in fishery resources, water quality, and habitat conditions in the Great Lakes would be encyclopedic, I confine discussion here to prime examples related to the most historically important fish resources. One of the values of the approach used in this manuscript is the collation in a single-source document of the conclusions reached by many scientists on reasons for changes in the fish resources across the Great Lakes basin.

Book chapter↗

Interactions between walleyes and smallmouth bass in a Missouri River reservoir with consideration of the influence of temperature and prey

Walleyes Sander vitreus are the most popular fish among South Dakota anglers, but smallmouth bass Micropterus dolomieu were introduced to provide new angling opportunities. Some walleye anglers have reported reductions in the quality of walleye fisheries since the introduction of smallmouth bass and attribute this to the consumption of young walleyes by smallmouth bass and competition for shared prey resources. We quantified the diets of walleyes and smallmouth bass in the lower reaches of Lake Sharpe (a Missouri River reservoir), calculated the diet overlap between the two predators, and determined whether they partitioned shared prey based on size. We also quantified walleye diets in the upper reach of the reservoir, which has a different prey base and allowed us to compare the growth rates of walleyes within Lake Sharpe. Age-0 gizzard shad Dorosoma cepedianum composed a substantial proportion of the diets of both predators, regardless of location, for most of the growing season; the patterns in shad vulnerability appeared to drive the observed patterns in diet overlap. Smallmouth bass appeared to consume a smaller size range of gizzard shad than did walleyes, which consumed a wide range. Smallmouth bass consumed Sander spp. in some months, but in very low quantities. Given that global climate change is expected to alter the population and community dynamics in Great Plains reservoirs, we also used a bioenergetics approach to predict the potential effects of limiting prey availability (specifically, the absence of gizzard shad and rainbow smelt Osmerus mordax ) and increased water temperatures (as projected from global climate change models) on walleye and smallmouth bass growth. The models indicated that the absence of rainbow smelt from the diets of walleyes in upper Lake Sharpe would reduce growth but that the absence of gizzard shad would have a more marked negative effect on both predators at both locations. The models also indicated that higher water temperatures would have an even greater negative influence on walleye growth; however, smallmouth bass growth was predicted to increase with higher temperatures. Fisheries managers should consider strategies to enhance the prey base or mitigate the effects of increased water temperatures that may occur in the future as a result of global climate change. Such proactive actions may alleviate potential future competition between walleyes and smallmouth bass resulting from changes in the fish community.

North American Journal of Fisheries Management↗

A definition of depletion of fish stocks

Attention was focused on the need of a common and better understanding of the term depletion as applied to the fisheries in order to eliminate if possible the existing inexactness of thought on the subject. Depletion has been confused at various times with at least ten different ideas associated with it but which, as has has heen pointed out, are not synonymous at all. In defining depletion we must recognize that the term represents a condition and must not he confounded with the cause (overfishing) that leads to this condition or with the symptoms that identify it. Depletion was defined as a reduction, through overfishing, in the level of abundance of the exploitable segment of a stock that prevents the realization of the maximum productive capacity.

Transactions of the American Fisheries Society↗

Contaminant levels in rainbow trout, Oncorhynchus mykiss, and their diets from Missouri coldwater hatcheries

Organochlorine and metal contaminants often occur in commercial fish diets and can accumulate in fish to levels of concern for human consumption. Contaminant levels were investigated in diet and rainbow trout fillets from Missouri coldwater hatcheries used in 'put and take' fisheries. The average fillet:diet ratio was <0.1 for lead and cadmium, 0.4-0.6 for organochlorine compounds, and about 0.8 for mercury. Trout fillet concentrations for all contaminants were low (<50 ng/g) and below Missouri's fish consumption advisory trigger levels. ?? 2008 Springer Science+Business Media, LLC.

Bulletin of Environmental Contamination and Toxico↗

Effect of stock size, climate, predation, and trophic status on recruitment of alewives in Lake Ontario, 1978-2000

The population of alewives Alosa pseudoharengus in Lake Ontario is of great concern to fishery managers because alewives are the principal prey of introduced salmonines and because alewives negatively influence many endemic fishes. We used spring bottom trawl catches of alewives to investigate the roles of stock size, climate, predation, and lake trophic status on recruitment of alewives to age 2 in Lake Ontario during 1978&ndash;2000. Climate was indexed from the temperature of water entering a south-shore municipal treatment plant, lake trophic status was indexed by the mean concentration of total phosphorus (TP) in surface water in spring, and predation was indexed by the product of the number of salmonines stocked and relative, first-year survival of Chinook salmon Oncorhynchus tshawytscha . A Ricker-type parent&ndash;progeny model suggested that peak production of age-1 alewives could occur over a broad range of spawning stock sizes, and the fit of the model was improved most by the addition of terms for spring water temperature and winter duration. With the addition of the two climate terms, the Ricker model indicated that when water was relatively warm in spring and the winter was relatively short, peak potential production of young was nine times higher than when water temperature and winters were average, and 73 times higher than when water was cold in spring and winters were long. Relative survival from age 1 to recruitment at age 2 was best described by a multiple linear regression with terms for adult abundance, TP, and predation. Mean recruitment of age-2 fish in the 1978&ndash;1998 year-classes predicted by using the two models in sequence was only about 20% greater than the observed mean recruitment. Model estimates fit the measured data exceptionally well for all but the largest four year-classes, which suggests that the models will facilitate improvement in estimates of trophic transfer due to alewives.

Transactions of the American Fisheries Society↗

Population characteristics of Ozark Bass (Ambloplites constellatus) in the upper White River basin of northern Arkansas

Ozark Bass ( Ambloplites constellatus ) is an understudied, endemic fish species in the Upper White River Basin of northern Arkansas. This study was part of an effort by fisheries managers to gather baseline data about the Ozark Bass to aid in understanding population dynamics and contribute to the limited data available for use in determining the efficacy of harvest regulations. Select population characteristics of Ozark Bass in two northern Arkansas streams were determined, population characteristics of Ozark Bass were compared to Shadow Bass ( Ambloplites ariommus ) and Rock Bass ( Ambloplites rupestris ) data collected from previous studies in southern Missouri, and relative condition, length-at-age, and annual survival of Ozark Bass were compared between sample streams. Sampling occurred in Crooked Creek and the Buffalo River during summer 2013 via boat electroshocking. Length and weight data were recorded for all Ozark Bass collected, and fish ages were determined through selective otolith retrieval and age-length keys. Ozark Bass in Crooked Creek had greater relative condition than Ozark Bass in Buffalo River ( P < 0.001). Neither Ozark bass lengths nor log-transformed weights differed ( P > 0.05) between sexes for fish collected from only the Buffalo River. Ozark Bass mean annual survival was similar between Crooked Creek (55% ± 5% as 95% confidence interval (CI)) and the Buffalo River (50% ± 7% CI) for fish age 2 to 9. Calculated Ozark Bass lengths-at-age for fish from both streams were comparable to the Von Bertalanffy growth estimates, except the Buffalo River age 7 categor y where there was only one observation. The relationship between Ozark Bass age and length differed between sampled streams, and variability in growth rates and length-at-age were observed among Ambloplites species. Results of this study contribute to the understanding of the population dynamics of the Ozark Bass that will lead to improved fisheries management.

Arkansas↗

What can volunteer angler tagging data tell us about the status of the Giant Trevally (ulua aukea) Caranx ignobilis fishery in Hawaii: revisiting data collected during Hawaii’s Ulua and Papio Tagging Project 2000-2016

Giant Trevally (ulua aukea) Caranx ignobilis is one of the most highly prized and frequently targeted nearshore species. However, there is very little information on its current status in Hawaiian waters. This study uses mark-recapture data collected as part of recreational angler tagging program conducted by the Hawaii Department of Land and Natural Resources-Division of Aquatic Resources during 2000-2012. Mark-recapture data were used to estimate von Bertalanffy growth curve parameters and survivorship. Growth curves generated from the markrecapture data suggested that Giant Trevally from the main Hawaiian Islands may be growing faster and reach a smaller maximum size than individuals in the Northwest Hawaiian Islands, but there are a number of issues rendering this conclusion uncertain. The survivorship of Giant Trevally was positively associated with age, in part due to ontogenetic habitat shifts that result in older fish moving to offshore habitats where they are less vulnerable to anglers. When compared to stock assessments performed using commercial landings data and fisheries-independent visual surveys, the mark-recapture data produced similar estimates for the average length of exploited fish, a metric highly negatively correlated to fishing mortality. These results emphasize the need for additional information on the biology of Giant Trevally in Hawaiian waters and suggest that the data collected from this recreational angler tagging program may be useful to generate reliable estimates of mortality for stock assessment purposes.

Hawaii↗

Conducting and interpreting fish telemetry studies: Considerations for researchers and resource managers

Telemetry is an increasingly common tool for studying the ecology of wild fish, with great potential to provide valuable information for management and conservation. For researchers to conduct a robust telemetry study, many essential considerations exist related to selecting the appropriate tag type, fish capture and tagging methods, tracking protocol, data processing and analyses, and interpretation of findings. For telemetry-derived knowledge to be relevant to managers and policy makers, the research approach must consider management information needs for decision-making, while end users require an understanding of telemetry technology (capabilities and limitations), its application to fisheries research and monitoring (study design), and proper interpretation of results and conclusions (considering the potential for biases and proper recognition of associated uncertainties). To help bridge this gap, we provide a set of considerations and a checklist for researchers to guide them in conducting reliable and management-relevant telemetry studies, and for managers to evaluate the reliability and relevance of telemetry studies so as to better integrate findings into management plans. These considerations include implicit assumptions, technical limitations, ethical and biological realities, analytical merits, and the relevance of study findings to decision-making processes.

Reviews in Fish Biology and Fisheries↗

Trade-offs in experimental designs for estimating post-release mortality in containment studies

Estimates of post-release mortality (PRM) facilitate accounting for unintended deaths from fishery activities and contribute to development of fishery regulations and harvest quotas. The most popular method for estimating PRM employs containers for comparing control and treatment fish, yet guidance for experimental design of PRM studies with containers is lacking. We used simulations to evaluate trade-offs in the number of containers (replicates) employed versus the number of fish-per container when estimating tagging mortality. We also investigated effects of control fish survival and how among container variation in survival affects the ability to detect additive mortality. Simulations revealed that high experimental effort was required when: (1) additive treatment mortality was small, (2) control fish mortality was non-negligible, and (3) among container variability in control fish mortality exceeded 10% of the mean. We provided programming code to allow investigators to compare alternative designs for their individual scenarios and expose trade-offs among experimental design options. Results from our simulations and simulation code will help investigators develop efficient PRM experimental designs for precise mortality assessment.

Fisheries Research↗

Understanding the influence of predation by introduced fishes on juvenile salmonids in the Columbia River Basin: Closing some knowledge gaps. Interim Report of Research 2010

Project overview Predation on juvenile salmonids by fish in the Columbia River Basin (CRB) has impacted salmon survival and is a topic that has received considerable attention over the last three decades. Some of the earliest and most detailed research focused on the food habits, consumption rates, abundance, and distribution of predaceous northern pikeminnow Ptychocheilus oregonensis , smallmouth bass Micropterus dolomieu , walleye Sander vitreus , and channel catfish Ictalurus punctatus in John Day Reservoir (Beamesderfer and Rieman 1991; Poe et al. 1991; Vigg et al. 1991). This group of researchers also estimated the loss of juvenile salmonids to predation by some of these predators (Rieman et al. 1991). Since this pioneering effort, others have evaluated various aspects of predation-related mortality on juvenile salmonids in the CRB, focusing mostly on northern pikeminnow and smallmouth bass (e.g., Tabor et al. 1993; Zimmerman 1999; Naughton et al. 2004). Perhaps the most significant finding coming from this body of research was that the native northern pikeminnow was the dominant predator of juvenile salmonids in the CRB. Indeed, Beamesderfer et al. (1996) estimated that northern pikeminnow consumed about 16 million (8%) of the estimated 200 million juvenile salmonids emigrating annually in the CRB, far surpassing the consumption of smallmouth bass, walleye, and channel catfish combined. Because of this, large-scale management fisheries (i.e., the northern pikeminnow management program, or NPMP; see Rieman and Beamesderfer 1990; Beamesderfer et al. 1996) have been implemented in the CRB since 1990 to achieve a 10%&ndash;20% exploitation rate on northern pikeminnow and reduce predation on juvenile salmonids. The NPMP has been a success, resulting in up to 38% potential reductions in predation (Friesen and Ward 1999; Knutsen and Ward 1999; Ward and Zimmerman 1999;). In contrast to the NPMP, Oregon and Washington state fish and wildlife agencies manage and enhance recreational fisheries for smallmouth bass and walleye by implementing size and harvest limit regulations. Recently, many biologists and fish managers have become concerned about the impact of non-native predaceous fishes on juvenile salmonid survival. For example, Poe et al. (1994) warned that smallmouth bass, walleye, and channel catfish were expanding their populations in some areas, that these fish could be significant predators on juvenile salmonids, and that they may compete with northern pikeminnow for common prey items, resulting in higher consumption rates of salmonids by the native predator. Sanderson et al. (2009) reported that the impact of non-indigenous species (including piscivorous fishes) on salmon survival within the CRB can be severe and suggested that managing nonindigenous species may be imperative for salmon recovery. Assessing the current ecological impacts of introduced fishes throughout the CRB will fill information gaps associated with their impact on salmonid survival and contribute to the description of CRB food webs. In response to these recent concerns about the potential predatory impact of non-native piscivores on salmon survival, the Bonneville Power Administration (BPA) and the Columbia Basin Fish and Wildlife Authority (CBFWA) co-hosted a workshop to address predation on juvenile salmonids in the CRB by non-native fish (Halton 2008). The purpose of the workshop was to review, evaluate, and develop strategies to reduce predation by non-native fishes on juvenile salmonids. In the end, discussion at the workshop and at subsequent meetings considered two potential ideas to reduce predation by non-native fish on juvenile salmonids; (1) understanding the role of juvenile American shad Alosa sapidissima in the diet of non-native predators in the fall; and (2) the effects of localized, intense reductions of smallmouth bass in areas of particularly high salmonid predation. In this report, we describe initial efforts to understand the influence of juvenile American shad as a prey item for introduced predators in the middle Columbia River. Our first objective, addressed in Chapter 1, was to evaluate the efficacy of nonlethal methods to describe the physiological condition of smallmouth bass, walleye, and channel catfish from late summer through late fall. Such information will be used to understand the contribution of juvenile American shad to the energy reserves of predaceous fish prior to winter. In Chapter 2, we describe the results of some limited sampling to document the food habits of smallmouth bass, walleye, and channel catfish in three reservoirs of the middle Columbia River during late fall. Collectively, we hope to increase our understanding of the contribution of juvenile American shad to the diets of introduced predators and the contribution of this diet to their energy reserves, growth, and perhaps over-winter survival. Managers should be able to use this information for deciding whether to control the population of American shad in the CRB or for managing introduced predaceous fish in the CRB.

Oregon, Washington↗