Recent changes in successional state of the deep-water fish communities of Lakes Michigan, Huron, and Ontario and management implications
No abstract available.
Geology topics
Publications and source records attributed to Brian F. Lantry.
No abstract available.
Lake trout Salvelinus namaycush were extirpated from Lake Ontario circa 1950 owing to commercial and recreational fishing, predation by sea lampreys Petromyzon marinus , and habitat degradation. Since the 1970s, substantial efforts have been devoted to reestablishing a self-sustaining population through stocking, sea lamprey control, and harvest reduction. Although a stocking-supported population has been established, only limited natural reproduction has been detected. Since the 1990s, surveys have indicated a continuing decline in overall abundance despite fairly static stocking levels. We constructed a statistical catch-at-age model to describe the dynamics of Lake Ontario lake trout from 1985 to 2007 and explore what factor(s) could be causing the declines in abundance. Model estimates indicated that abundance had declined by approximately 76% since 1985. The factor that appeared most responsible for this was an increase in age-1 natural mortality rates from approximately 0.9 to 2.5 between 1985 and 2002. The largest source of mortality for age-2 and older fish was sea lamprey predation, followed by natural and recreational fishing mortality. Exploitation was low, harvest levels being uncertain and categorized by length rather than age. Accurate predictions of fishery harvest and survey catch per unit effort were obtained despite low harvest levels by using atypical data (e.g., numbers stocked as an absolute measure of recruitment) and a flexible modeling approach. Flexible approaches such as this might allow similar assessments for a wide range of lightly exploited stocks. The mechanisms responsible for declining age-1 lake trout survival are unknown, but the declines were coincident with an increase in the proportion of stocked fish that were of the Seneca strain and a decrease in the overall stocking rate. It is possible that earlier studies suggesting that Seneca strain lake trout would be successful in Lake Ontario are no longer applicable given the large ecosystem changes that have occurred subsequent to invasion by dreissenid mussels.
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 1978–2000. 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–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 1978–1998 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.
Hemimysis anomala , a Ponto-Caspian littoral mysid, is an emerging Great Lakes invader that was discovered in Lakes Michigan and Ontario in 2006. Similar to the native mysid Mysis diluviana , Hemimysis exhibits a diel vertical migration pattern but generally inhabits shallower and warmer waters than M. diluviana . Because basic information on the distribution, habitat use, and biology of Hemimysis in the Great Lakes is scarce, the potential for food web disruption by Hemimysis cannot easily be predicted. Preliminary observations indicate widespread invasion of Hemimysis in Lake Ontario. In this study, we confirm the presence of Hemimysis at sites spanning the northern and southern shores of Lake Ontario and the presence of the individuals during winter months. In one horizontal tow in November 2007, over 26,000 individuals were collected with a length range of 4.4 to 9.0. mm and an average caloric density of 611. cal/g wet weight. The most effective methods for sampling Hemimysis were horizontal tows with either a zooplankton net in the water column or a benthic sled near the lake bottom. Although more quantitative data on the life history and distribution of this species is necessary, our preliminary observations support the prediction that the potential for Hemimysis to impact the nearshore food web in Lake Ontario appears high.
The lake whitefish (Coregonus clupeaformis) was an important member of the native fish community and a valued commercial species in Lake Ontario. Lake whitefish were common in U.S. waters of the lake until 1965 and very abundant in Canadian waters through the early 1970s, although their numbers declined shortly thereafter. During 1975-1985, lake whitefish stocks remained depressed throughout the lake as a result of the combined effects of degraded water quality, overfishing, and predation. Rainbow smelt (Osmerus mordax) probably preyed on whitefish fry, and sea lamprey (Petromyzon marinus) preyed on adults. During 1985-1987, lake whitefish stocks began to recover in eastern Lake Ontario, and their buildup continued into the mid-1990s. Reasons for the recovery likely included control of the sea lamprey population and a reduction in the number of piscivorous rainbow smelt. By 1997, lake whitefish abundance had declined severely again; some fish appeared to have dispersed from the northeastern to the southeastern regions of the lake, and the depth of capture increased. We believe that the collapse of Diporeia spp. populations during 1992-1999 was responsible for the decline in the lake whitefish populations and the shifts in geographic and bathymetric distribution because lake whitefish fed primarily on Diporeia spp. After the collapse of Diporeia spp. populations, lake whitefish in southeastern Lake Ontario fed on Mysis relicta and quagga mussels (Dreissena bugensis). Changing from a diet of high-lipid Diporeia spp to low-lipid dreissenids and foraging on Mysis relicta at lower temperatures are apparently hampering the rebuilding of lake whitefish stocks.
The authors document the status of Lake Ontario's open-water fish community in 1972, near the beginning of an era of massive fish stocking and when phosphorus levels in the lake from anthropogenic inputs, were near their peak. They then describe changes that occurred in the fish community in 1978-98. This was a period when large numbers of young salmonid piscivores were released annually, sea lamprey control continued to improve, and phosphorus levels were declining due to successful nutrient abatement programs. Coincident with the above, the lower food web was changed by the addition of new exotic invertebrates, the zooplankter Bythotrephes cederstroemi and particularly the zebra mussel, Dreissena polymorpha, and quagga mussel, D. bugensis. The picture of the fish community structure is drawn from records of catches in bottom trawls and gill nets during surveys of southern Lake Ontario conducted the the U.S. Geological Survey (USGS) and the New York Department of Environmental Conservation (NYDEC), from records of fish stocked in Lake Ontario by the NYDEC, and from a creel census of boat anglers returning to southern Lake Ontario ports conducted by the NYDEC.
The authors conclude that small numbers of lake trout spawned successfully each year during 1992-97 in Lake Ontario, although this has yet to result in a trend of increasing natural reproduction. Juxtaposed with the high abundance of mature fish (Selgeby et al., 1995), the situation in Lake Ontario suggests a reduction in reproductive efficiency. This could result from mortality factors that may to a certain extent be density independent because recruitment has remained flat in the face of increasing spawner abundance. According to RESTORE, such factors are likely acting during the first year of life. Accordingly, the authors herin review the evidence that former barriers to lake trout reproduction in Lake Ontario that act as early-life-stage bottlenecks have been removed. In addition, the authors review other potential new barriers for which there has only recently been enough information to judge their relative importance.
Available population and diet data on double-crested cormorant ( Phalacrocorax auritus ) and smallmouth bass ( Micropterus dolomieui ) numbers, demographics, and exploitation rates were synthesized to examine the relationship between cormorant and smallmouth bass abundance in the U.S. waters of the eastern basin of Lake Ontario. It was found that after the number of cormorants nesting on Little Galloo Island in New York exceeded 3,500 pairs in 1989, survival of young smallmouth bass, not yet of legal size for the sport harvest (< 305 mm), began to decline. Despite production of strong year classes in 1987 and 1988, abundance of smallmouth bass measured from gill net surveys declined to its lowest level by 1995 and remained there through 1998. Stable or increasing catch and harvest rates in other local fisheries along the U.S. shore suggested that declines in smallmouth bass abundance in the eastern basin were not related to water quality. Stable or increasing growth rates for smallmouth bass age 2 and older since the 1980s further indicated that food resource limitation was also not the cause for declines in abundance. Comparisons of estimates of size and age-specific predation on smallmouth bass by cormorants with projected smallmouth bass population size indicated that much of the increased mortality on young smallmouth bass, could be explained by cormorant predation.
In the mid-1990s, biologists conducting assessments of fish stocks in Lake Ontario reported finding alewives Alosa pseudoharengus , rainbow smelt Osmerus mordax , and juvenile lake trout Salvelinus namaycush at greater depths than in the mid-1980s. To determine if depth distributions shifted coincident with the early 1990s colonization of Lake Ontario by exotic Dreissena mussels, we calculated mean depth of capture for each of the three species during trawl surveys conducted annually during 1978–1997 and examined the means for significant deviations from established patterns. We found that mean capture depth of alewives, rainbow smelt, and age-2 lake trout shifted deeper during the build up of the dreissenid population in Lake Ontario but that timing of the shift varied among seasons and species. Depth shifts occurred first for rainbow smelt and age-2 lake trout in June 1991. In 1992, alewives shifted deeper in June followed by age-2 lake trout in July–August. Finally, in 1993 and 1994, the distribution of lake trout and alewives shifted in April–May. Reasons why the three fishes moved to deeper water are not clear, but changes in distribution were not linked to temperature. Mean temperature of capture after the depth shift was significantly lower than before the depth shift except for alewives in April–May. Movement of alewives, rainbow smelt, and age-2 lake trout to colder, deeper water has the potential to alter growth and reproduction schedules by exposing the fish to different temperature regimes and to alter the food chain, increasing predation on Mysis relicta in deep water and decreasing alewife predation on lake trout fry over nearshore spawning grounds in spring.
We compared predatory demand by pelagic planktivorous prey fish with invertebrate production in Lake Michigan during 1987 and in Lake Ontario during 1990. Predation by the planktivores in Lake Ontario was nearly fourfold higher than in Lake Michigan (approx. 87 g wet weight∙m −2 ∙year −1 ). Predation rates on Mysis were comparable in Lakes Michigan and Ontario (approx. 21 g∙m −2 ∙year −1 ), while predation on Diporeia was markedly higher in Lake Michigan than in Lake Ontario (21.3 vs. 8.5 g wet weight∙m −2 ∙year −1 ). In Lake Ontario, predatory demand on zooplankton exceeded our best estimate of production by a factor of 1.7. Similarly, predation estimates on Mysis in Lake Ontario were 1.2–2.0 times the estimated rate of production, depending on the production model used. Lake Michigan planktivores consumed approximately 55% of available zooplankton production in 1987, indicating that competition for prey resources, if operating, was not as intense as that in Lake Ontario in 1990. It is unclear how to resolve the paradox that predation could markedly exceed available prey production in some cases. There could be sources of error in the estimates of both the supply and demand sides of these trophic relationships.
We describe dynamics of energy density and size of Lake Ontario alewife Alosa pseudoharengus and rainbow smelt Osmerus mordax , and we use a bioenergetics model of a common pelagic piscivore, chinook salmon Oncorhynchus tshawytscha , to demonstrate the effect of these factors on piscivore daily ration during 1978–1990. The energy density of alewives varied more than twofold between peaks in September (age 1) or October–November (age ≥2) and the lows in May (age 1) or July–September (age≥2). The previously described seasonal pattern of energy density of Lake Michigan alewives was similar except that energy density of older alewives (age≥3) was markedly higher in Lake Michigan. During 1978–1990, the spring energy density of Lake Ontario alewives peaked in 1979 (6,259 J/g wet weight), declined irregularly until 1985, and then remained stable through 1990 (at approximately 4,600 J/g). The initial decline may have been a density-dependent response to a burgeoning alewife population, but the lack of an increase in alewife condition in the late 1980s, when alewife biomass fell, suggests a decline in lake productivity. Energy density of rainbow smelt increased with age in Lake Ontario and condition was invariant during 1978–1990 despite a threefold change in rainbow smelt biomass. Rainbow smelt energy density was lower and fluctuated less seasonally in Lake Ontario than in Lake Michigan. Mean weight of alewives aged 2 and older dropped from 41 g in 1978 to 19 g in 1989 in Lake Ontario. Rainbow smelt aged 2 and older showed a drop in mean weight from 13–17 g in 1978–1982 to 8 g in 1990. This downward trend in mean size of alewives was correlated with the sizes of alewives consumed by Lake Ontario chinook salmon during 1983–1987. For adult chinook salmon to maintain a constant growth rate during 1978–1990, mean individual daily ration during June–October had to increase from a low of 2.2% body weight/d (or 1.5 prey fish/d) in 1979 to 3.1% body weight/d (3.7 prey fish/d) in 1988. This increase in forage demand may have caused the observed declines in individual condition of salmonines over this period.