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Derek H. Ogle

Publications and source records attributed to Derek H. Ogle.

7 recordsLinked to original sources

A synthesis of the biology and ecology of sculpin species in the Laurentian Great Lakes and implications for the adaptive capacity of the benthic ecosystem

The Laurentian Great Lakes have experienced recent ecosystem changes that could lead to reductions in adaptive capacity and ultimately a loss of biodiversity and production throughout the food web. Observed changes in Great Lakes benthic communities include declines of native species and widespread success of invasive species like dreissenid mussels in all but Lake Superior. Understanding the ecology of native benthic deepwater preyfish and the reasons for their declines is important for predicting future losses in adaptive capacity and diversity, as well as managing the Great Lakes ecosystem to avoid such losses. Native sculpin species ( Cottus bairdii , C. cognatus , C. ricei , Myoxocephalus thompsonii ) historically were among the most abundant of the Great Lakes native deepwater benthic preyfish community and are an important link between offshore benthic and pelagic food webs. With one exception, these species have declined in abundance throughout the Great Lakes in recent years, but relatively little is known about their biology and ecology. This review synthesizes the available knowledge for the Great Lakes sculpin species and provides suggestions for future research efforts, which include understanding reproductive ecology and spawning behavior, connectivity and dispersal of populations, early life history, and influences of interactions with native and non-native species.

Great Lakes↗

Size and age of Stonecats in Lake Champlain; Estimating growth at the margin of their range to aid in population management

Little is known about populations of Stonecat Noturus flavus , especially in the northeastern United States, where they are at the edge of their range. In Lake Champlain tributaries, Stonecats are listed as endangered in Vermont but not in New York. Here we describe the growth of Stonecats in two tributaries to Lake Champlain, one in Vermont (LaPlatte River), which was our primary interest, and one in New York (Great Chazy River), with von Bertalanffy growth models fit to lengths at the times of marking and recapture and to observed length and age data. We also compared growth of Stonecats in these waters to results from other locations near the middle of their distribution. Stonecats in the Great Chazy River were larger at ages 1–3, but similar in size for ages 4 and 5, than Stonecats from the LaPlatte River. Stonecats in Lake Champlain tributaries were generally larger at age than those from the middle of their range, except for those from Lake Erie. From our mean length‐at‐age results and previous literature estimates of length at maturity for Stonecats, it appears that Stonecats in Lake Champlain reach maturity by age 3, though future research that directly estimates age at maturity would be more informative. These results will help managers assess the effect of various environmental and human stressors that Stonecats have experienced in the Lake Champlain basin in recent years. Furthermore, our results expand the literature, which lacks information about growth of this species. Finally, our mark–recapture approach to estimating growth of Stonecats can be applied to other species, especially where data are limited because of their status, and in other systems.

New York, Vermont↗

Estimating age at a specified length from the von Bertalanffy growth function

Estimating the time required (i.e., age) for fish in a population to reach a specific length (e.g., legal harvest length) is useful for understanding population dynamics and simulating the potential effects of length-based harvest regulations. The age at which a population reaches a specific mean length is typically estimated by fitting a von Bertalanffy growth function to length-at-age data and then rearranging the best-fit equation to solve for age at the specified length. This process precludes the use of standard frequentist methods to compute confidence intervals and compare estimates of age at the specified length among populations. We provide a parameterization of the von Bertalanffy growth function that has age at a specified length as a parameter. With this parameterization, age at a specified length is directly estimated, and standard methods can be used to construct confidence intervals and make among-group comparisons for this parameter. We demonstrate use of the new parameterization with two data sets.

North American Journal of Fisheries Management↗

Age, year‐class strength variability, and partial age validation of Kiyis from Lake Superior

ge estimates of Lake Superior Kiyis Coregonus kiyi from scales and otoliths were compared and 12 years (2003–2014) of length frequency data were examined to assess year‐class strength and validate age estimates. Ages estimated from otoliths were precise and were consistently older than ages estimated from scales. Maximum otolith‐derived ages were 20 years for females and 12 years for males. Age estimates showed high numbers of fish of ages 5, 6, and 11 in 2014, corresponding to the 2009, 2008, and 2003 year‐classes, respectively. Strong 2003 and 2009 year‐classes, along with the 2005 year‐class, were also evident based on distinct modes of age‐1 fish (<110 mm) in the length frequency distributions from 2004, 2010, and 2006, respectively. Modes from these year‐classes were present as progressively larger fish in subsequent years. Few to no age‐1 fish (<110 mm) were present in all other years. Ages estimated from otoliths were generally within 1 year of the ages corresponding to strong year‐classes, at least for age‐5 and older fish, suggesting that Kiyi age may be reliably estimated to within 1 year by careful examination of thin‐sectioned otoliths.

North American Journal of Fisheries Management↗

Burrowing mayfly populations in Chequamegon Bay, Wisconsin: 2002 and 2012

Burrowing mayflies (Ephemeroptera: Ephemeridae) are sensitive to pollution and have been used as environmental indicators in the Great Lakes. Hexagenia limbata and Ephemera simulans population abundance and biomass estimates from Chequamegon Bay, Lake Superior, were compared between the years 2002 and 2012 as well as inside and outside the Northern States Power Lakefront Superfund site. Mean abundance was similar and mean biomass of Ephemeridae was slightly less in 2012 than in 2002, most likely due to the occurrence of E. simulans in 2012, a smaller species not collected in 2002. In 2012, mean ephemerid abundance and biomass outside the Superfund site was significantly higher than inside the Superfund site. Biomass was higher in clay, clay with sand, and sand with clay substrates than in fine sand, coarse sand, or wood debris substrates. Substrate in the Superfund site was predominantly wood debris. Future monitoring of ephemerid populations in Chequamegon Bay, and particularly in the Superfund site as clean up begins, would be valuable to establish long-term population trends for these two species and potentially shed light on the habitat requirements of E. simulans , an understudied species in the Great Lakes.

Chequamegon Bay;Great Lakes;Lake Superior↗

Predation on ruffe by native fishes of the St. Louis River Estuary, Lake Superior, 1989-1991

The ruffe Gymnocephalus cernuus , an exotic Eurasian percid, recently became established in the St. Louis River estuary, Lake Superior, after accidental introduction. Management actions (catch regulations and stockings) were enacted in 1989 to increase the density of top-level predators in the estuary, and thus to increase predation on ruffe. We conducted a field and laboratory study to determine if, and to what extent, native piscivores consume ruffe. Stomachs of 3,669 predators were examined in 1989&ndash;1991. Ruffe occurred in 6.7% of burbot Lota lota , 5.8% of bullheads Ictalurus spp., 4.7% of smallmouth bass Micropterus dolomieu , 2.6% of northern pike Esox lucius , 2.6% of black crappies Pomoxis nigromaculatus , and 1.3% of yellow perch Perca flavescens (4.5% after 1989) captured during the 3-year study. No ruffe were found in 967 stomachs of walleyes Stizostedion vitreum examined. Ruffe were 22.7%, of the diet (by weight) of bullheads (during the only year bullheads were captured) and 0.1&ndash;17.9% of the diet of northern pike. Ruffe were 0.9&ndash;24.5% of the diet of smallmouth bass that contained fish, 1.5&ndash;6.9% of yellow perch that contained fish, and 0.0&ndash;10.9% of black crappies that contained fish. Most ruffe eaten were age-0 or small age- 1 fish. In the laboratory, walleyes that were first fed soft-rayed prey or that were also offered soft-rayed prey consumed very few ruffe, whereas walleyes that were first fed spiny-rayed yellow perch or were also offered yellow perch consumed about equal numbers of ruffe and yellow perch. Northern pike and burbot consumed about equal numbers of ruffe and yellow perch in the laboratory. It is unlikely that predation will effectively control the initial expansion of ruffe in other areas of the Great Lakes because native predators initially consume few ruffe, especially if more preferred soft-rayed prey are available.

North American Journal of Fisheries Management↗

Diet and feeding periodicity of ruffe in the St. Louis River estuary, Lake Superior

Ruffe Gymnocephalus cernuus , a percid native to Europe and Asia, is established in the Lake Superior drainage and could have negative impacts on native fish through competition for forage and predation on fish eggs. We investigated the diet of ruffes in the 4,654-ha St. Louis River estuary in May&ndash;October 1989&ndash;1990 and the feeding periodicity of ruffes in two adjacent habitats during five 24-h periods in summers 1990&ndash;1991. Ruffes were primarily benthophagous. Age-0 ruffes fed mostly on cladocerans and copepods in early summer and midge larvae (Chironomidae) in late summer and fall. Adult ruffes less than 12 cm fed mostly on midges and other macrobenthos but also consumed large numbers of microcrustaceans. Adult ruffes 12 cm and larger fed mostly on midges, burrowing mayflies Hexagenia spp., and caddisflies (Trichoptera). Ruffes consumed few fish eggs. Adult ruffes in deeper waters and all age-0 ruffes fed throughout the day as indicated by weight patterns of stomach contents. However, adult ruffes generally moved to shallower waters at night to feed most heavily. Results of this study indicate that ruffes will probably compete with other benthic-feeding fishes such as yellow perch Perca flavescens and trout-perch Percopsis omiscomaycus .

Transactions of the American Fisheries Society↗