The Great Lakes Acoustic Telemetry Observation System (GLATOS), organized in 2012, aims to advance and improve conservation and management of Great Lakes fishes by providing information on behavior, habitat use, and population dynamics. GLATOS faced challenges during establishment, including a funding agency-imposed urgency to initiate projects, a lack of telemetry expertise, and managing a flood of data. GLATOS now connects 190+ investigators, provides project consultation, maintains a web-based data portal, contributes data to Ocean Tracking Network’s global database, loans equipment, and promotes science transfer to managers. The GLATOS database currently has 50+ projects, 39 species tagged, 8000+ fish released, and 150+ million tag detections. Lessons learned include (1) seek advice from others experienced in telemetry; (2) organize networks prior to when shared data is urgently needed; (3) establish a data management system so that all receivers can contribute to every project; (4) hold annual meetings to foster relationships; (5) involve fish managers to ensure relevancy; and (6) staff require full-time commitment to lead and coordinate projects and to analyze data and publish results.
We quantified the relationship between lake size and abundance of walleyes Stizostedion vitreum at two life stages, age 0 and adult, in 172 northern Wisconsin lakes. We also determined if the relationship varied with recruitment source (stocked or natural) in order to evaluate the current system of management. For adult walleyes, as estimated by mark-recapture in spring, abundance was linearly related to lake surface area. Age-0 walleye abundance estimated by fall electrofishing catch was also linearly related to the miles of shoreline surveyed. Lake surface area explained 59% of the variability in adult walleye abundance across lakes ranging in size from 93 to 15,300 acres. Lake surface area explained 61% of the variation in abundance of self-sustaining walleye populations and 65% of stocked populations. Walleye abundance was higher in lakes sustained by natural reproduction than in lakes sustained by stocking. These patterns in abundance based on recruitment source were also apparent at age 0. We conclude that differences in abundance between self-sustaining and stocked walleye populations in northern Wisconsin lakes may be established during the first year, possibly due in part to recruitment source.
Life history characteristics (age, growth, survival, and maturity) were compared between the deepwater “humper” and shallow‐water “lean” forms of lake trout Salvelinus namaycush in Lake Mistassini, Quebec, to determine whether the two morphotypes may represent resource polymorphism. Lake trout were sampled using graded‐mesh (range = 51–114 mm stretch) gill nets set in deep and shallow waters. Humpers were typically caught in deep waters (>50 m) and averaged 474 mm TL (range = 389–616 mm) and 852 g in weight (range = 470–1,710 g), whereas leans were typically caught in shallow waters (<50 m) and averaged 525 mm TL (range = 301–865 mm) and 1,210 g in weight (range = 200–6,500 g). Humpers and leans did not differ in weight–length relationships and grew slimmer with length over a common TL range (389–616 mm). Average age of humpers was 27 years (range = 13–49 years); average age of leans was 21 years (range = 6–42 years). The two forms did not differ in total annual mortality (A) of fish older than 17 years, the first age beyond which numbers declined with age for both morphs (A = 5.1%; 95% confidence interval = 2.4–7.8%). Humpers grew slower (annual growth rate ω = 53 mm/year) than leans (ω = 68 mm/year) and to a shorter mean asymptotic length (L∞ = 514 mm) than leans (L∞ = 605 mm). Mature humpers (mean TL = 475 mm, SE = 9.0; N = 58) were shorter on average than mature leans (mean TL = 539 mm, SE = 8.5; N = 65); mature humpers (mean age = 27 years, SE = 1.0; N = 56) were also older on average than mature leans (mean age = 23 years, SE = 0.98; N = 61). We conclude that lean and humper forms of lake trout in Lake Mistassini differed in age, growth, and maturity; this is consistent with the resource polymorphism that has been observed for other lake trout populations and other char species.
Stunting in populations of bluegill Lepomis macrochirus is a major management problem in the upper midwestern United States, Traditionally, stunting has been attributed to a lack of food resources. An alternative theory suggests that stunting may result from harvest of the large parental males that inhibit spawning by smaller males, allowing small males to direct energy to reproduction instead of to growth. We used a population model to simulate restrictions on harvest of large males under various conditions of vulnerability to angling, growth rate, and angler effort. Regulations tested were a daily bag of 5 fish and seasonal bags of 50 fish or 50 fish but only 1 trophy specimen (>180 mm total length); a limit of only 1 trophy fish during the spawning season; and a spawning season closure. Growth and angler effort had the greatest effects on size structure in simulated bluegill populations; high growth and low effort led to notable increases in mean fish length. Tested regulations and male vulnerability to angling had little effect on size structure although spawning season closure produced a modest increase in mean length. The simulations also suggested that increases in the proportion of large fish in bluegill populations require regulations that reduce total angler effort. Furthermore, to be successful, effort regulations must be applied to populations that have the potential for good growth.
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