Fish assemblages that include northern pike Esox lucius as a dominant predator were sampled in 19 small (<120 ha) northern Wisconsin lakes. The purpose of this sampling was to describe northern pike population characteristics and identify factors affecting growth rates. Fish assemblages in these lakes were dominated by centrarchids, primarily bluegill Lepomis macrochirus, and small fusiform species such as yellow perch Perca flavescens. Northern pike population size structures were typically truncated at around 53 cm. Average density of northern pike (≥35 cm) was 16.1 fish/ha and ranged 2.8–38.0 fish/ha. Growth of northern pike decreased, in comparison with a growth standard, as early as age 4. Most northern pike were less than age 6, and few fish were older than age 8. Diet of northern pike generally indicated opportunistic feeding strategies with some preference for fusiform prey. Multiple factors were identified as potentially limiting northern pike growth and size structure. Northern pike growth was negatively related to northern pike density, water transparency (Secchi depth), and abundance of small bluegills. Extensive littoral areas, water temperatures greater than 21°C during the growing season, and winterkill also limit northern pike growth and size structure. Effective management of these small lakes will probably require an individual‐lake approach to identify specific mechanisms limiting growth.
Conservation of genetic resources is a challenging issue for agencies managing popular sport fishes. To address the ongoing potential for genetic risks, we developed a comprehensive set of recommendations to conserve genetic diversity of muskellunge (Esox masquinongy) in Wisconsin, and evaluated the extent to which the recommendations can be implemented. Although some details are specific to Wisconsin's muskellunge propagation program, many of the practical issues affecting implementation are applicable to other species and production systems. We developed guidelines to restrict future broodstock collection operations to lakes with natural reproduction and to develop a set of brood lakes to use on a rotational basis within regional stock boundaries, but implementation will require considering lakes with variable stocking histories. Maintaining an effective population size sufficient to minimize the risk of losing alleles requires limiting broodstock collection to large lakes. Recommendations to better approximate the temporal distribution of spawning in hatchery operations and randomize selection of brood fish are feasible. Guidelines to modify rearing and distribution procedures face some logistic constraints. An evaluation of genetic diversity of hatchery‐produced fish during 2008 demonstrated variable success representing genetic variation of the source population. Continued evaluation of hatchery operations will optimize operational efficiency while moving toward genetic conservation goals.
Mark-recapture studies are an important component of fisheries research and management. Underlying assumptions of such studies include minimal tag loss and negligible effects on the behavior, fitness, and survival of tagged individuals. Passive integrated transponder (PIT) tags are becoming increasingly commonplace, largely because of their small size, ease of implantation, longevity, and reportedly high rates of retention. We evaluated tag retention and survival and growth effects on age-0 muskellunge Esox masquinongy marked with PIT tags at two implantation sites, the peritoneal cavity and the dorsal musculature, during overwinter trials in Illinois and Wisconsin. For both trials, no significant differences in survival (88.0-89.8%), relative daily growth (0.0006-0.00062 mmÁmm À1 Ád À1 ), or tag retention (99.5-99.8%) were observed among the two implantation groups and a control group. Survival and tag retention were also similar between trials. Our findings suggest that PIT tags implanted either in the peritoneal cavity or the dorsal musculature are acceptable for use in marking age-0 muskellunge.
Accurate age estimates are critical for understanding life histories of fishes and developing management strategies for fish populations. However, validation of age estimates requires known-age fish, which are often lacking. We used known-age (ages 1–25) muskellunge (Esox masquinongy) to determine the precision and accuracy of age estimates from fin rays. We also determined whether fin location (anal or pelvic), fin ray number, and preparation methods affected accuracy and precision. Lastly, we determined whether von Bertalanffy growth parameters estimated from fin ray ages were similar to parameters estimated from known ages. Precision and accuracy of age estimates from anal and pelvic rays were similar and estimates were relatively precise (coefficient of variation = 8.5%) and accurate (mean absolute difference from known age = 0.85 years) for ages 4–15, but ages were overestimated for younger fish and underestimated for older fish. Growth models based on estimated age were similar to models based on known age. Anal and pelvic rays offer a nonlethal alternative for age estimation of muskellunge ages 4–15 and for producing reliable estimates of growth.
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