Sea Lamprey (Petromyzon marinus) Predation on Freshwater Teleosts

1973 ◽  
Vol 30 (5) ◽  
pp. 601-605 ◽  
Author(s):  
G. J. Farmer ◽  
F. W. H. Beamish

The incidence of attack by the sea lamprey (Petromyzon marinus) was studied on freshwater teleosts of similar and different size. Splake (Salvelinus namaycush × Salvelinus fontinalis), carp (Cyprinus carpio), and white suckers (Catostomus commersoni) were attacked a significantly greater number of times than lake whitefish (Coregonus clupeaformis), burbot (Lota lota), shorthead redhorse suckers (Moxostoma macrolepidotum), and brown bullheads (Ictalurus nebulosus). Lampreys rarely preyed upon walleye (Stizostedion vitreum vitreum). Most attacks occurred between the head and caudal peduncle below the lateral line and particularly in the region behind the pectoral fins. Lampreys attacked the largest individuals of any species more frequently than the smaller representatives. The presence of lampreys on a fish did not further the incidence of attack on that fish. None of the species of fish appeared to avoid lamprey attacks, nor did they avoid fish on which lampreys were attached. Only rarely were fish observed to dislodge lampreys.

1980 ◽  
Vol 37 (11) ◽  
pp. 1989-2006 ◽  
Author(s):  
Everett Louis King Jr.

Criteria for the classification of marks inflicted by sea lamprey (Petromyzon marinus) into nine categories were developed from laboratory studies in an attempt to refine the classification system used in field assessment work. These criteria were based on characteristics of the attachment site that could be identified under field conditions by unaided visual means and by touching the attachment site. Healing of these marks was somewhat variable and was influenced by the size of lamprey, duration of attachment, severity of the wound at lamprey detachment, season and water temperature, and by other less obvious factors. Even under laboratory conditions staging of some wounds was difficult, especially at low water temperatures. If these criteria are to be used effectively and with precision in the field, close examination of individual fish may be required. If the feeding and density of specific year-classes of sea lampreys are to be accurately assessed on an annual basis, close attention to the wound size (as it reflects the size of the lamprey's oral disc) and character of wounds on fish will be required as well as consideration of the season of the year in which they are observed.Key words: sea lamprey, attack marks, lake trout, Great Lakes


1980 ◽  
Vol 37 (11) ◽  
pp. 2057-2062 ◽  
Author(s):  
A. H. Lawrie ◽  
W. MacCallum

The Lake Superior lake trout (Salvelinus namaycush) population is being rebuilt following its collapse in the early 1950s. Estimates are presented of the contributions to this recovery provided directly by the artificial recruitment of hatchery fish, a demonstrable amelioration in mortality rates and a resurgence, lately, of natural recruitment. Of the increased lake trout abundance, 55% on the average was owing to trebling the planting density, 40% to improved survival, and 5% to increasing recruitment of native lake trout. The precise contribution of the sea lamprey (Petromyzon marinus) control program could not be defined for lack of sufficient early data.Key words: lake trout, sea lamprey, rehabilitation, natural recruitment, hatchery stocking


2002 ◽  
Vol 59 (4) ◽  
pp. 736-753 ◽  
Author(s):  
Charles P Madenjian ◽  
Gary L Fahnenstiel ◽  
Thomas H Johengen ◽  
Thomas F Nalepa ◽  
Henry A Vanderploeg ◽  
...  

Herein, we document changes in the Lake Michigan food web between 1970 and 2000 and identify the factors responsible for these changes. Control of sea lamprey (Petromyzon marinus) and alewife (Alosa pseudoharengus) populations in Lake Michigan, beginning in the 1950s and 1960s, had profound effects on the food web. Recoveries of lake whitefish (Coregonus clupeaformis) and burbot (Lota lota) populations, as well as the buildup of salmonine populations, were attributable, at least in part, to sea lamprey control. Based on our analyses, predation by salmonines was primarily responsible for the reduction in alewife abundance during the 1970s and early 1980s. In turn, the decrease in alewife abundance likely contributed to recoveries of deepwater sculpin (Myoxocephalus thompsoni), yellow perch (Perca flavescens), and burbot populations during the 1970s and 1980s. Decrease in the abundance of all three dominant benthic macroinvertebrate groups, including Diporeia, oligochaetes, and sphaeriids, during the 1980s in nearshore waters ([Formula: see text]50 m deep) of Lake Michigan, was attributable to a decrease in primary production linked to a decline in phosphorus loadings. Continued decrease in Diporeia abundance during the 1990s was associated with the zebra mussel (Dreissena polymorpha) invasion, but specific mechanisms for zebra mussels affecting Diporeia abundance remain unidentified.


1988 ◽  
Vol 45 (8) ◽  
pp. 1406-1410 ◽  
Author(s):  
Roger A. Bergstedt ◽  
Clifford P. Schneider

During 1982–85, 89 dead fake trout (Salvelinus namaycush) were recovered with bottom trawls in U.S. waters of Lake Ontario: 28 incidentally during four annual fish-stock assessment surveys and 61 during fall surveys for dead fish. During the assessment surveys, no dead lake trout were recovered in April–June, one was recovered in August, and 27 were recovered in October or November, implying that most mortality from causes other than fishing occurred in the fall. The estimated numbers of dead lake trout between the 30- and 100-m depth contours in U.S. waters ranged from 16 000 (0.08 carcass/ha) in 1983 to 94 000 (0.46 carcass/ha) in 1982. Of 76 carcasses fresh enough to enable recognition of sea lamprey (Petromyzon marinus) wounds, 75 bore fresh wounds. Assuming that sea lamprey wounding rates on dead fish were the same as on live ones of the same length range (430–740 mm), the probability of 75 of the 76 dead lake trout bearing sea lamprey wounds was 3.5 × 10−63 if death was independent of sea lamprey attack, thus strongly implicating sea lampreys as the primary cause of death of fish in the sample. The recovery of only one unwounded dead lake trout also suggested that natural mortality from causes other than sea lamprey attacks is negligible.


1980 ◽  
Vol 37 (11) ◽  
pp. 2063-2073 ◽  
Author(s):  
Richard L. Pycha

Total mortality rates of lake trout (Salvelinus namaycush) of age VII and older from eastern Lake Superior were estimated from catch curves of age distributions each year in 1968–78. The instantaneous rate of total mortality Z varied from 0.62 to 2.31 in close synchrony with sea lamprey (Petromyzon marinus) wounding rates on lake trout. The regression of transformed Z on the index of lamprey wounding, accounted for over 89% of the variation in lake trout mortality (r2 = 0.893). An iterative method of estimating rates of exploitation u, instantaneous rates of fishing mortality F, K (a constant relating sample catch per unit effort to population size), instantaneous normal natural mortality rate M, and instantaneous rate of mortality due to sea lamprey predation L from the sample catch per unit effort and total catch by the fishery is presented. A second method using the results of a 1970–71 tagging study to estimate the mean F in 1970–77 yielded closely similar results to the above and is presented as corroboration. The estimates of u, F, and M appear to be reasonable. F ranged from 0.17 in 1974 to 0.42 in 1969 and M was estimated at 0.26. L varied from 0.21 in 1974 to 1.70 in 1968. Management implications of various policies concerning sea lamprey control, exploitation, and stocking are discussed.Key words: lake trout, sea lamprey, lamprey control, mortality, predation, Lake Superior, fishery, management


1980 ◽  
Vol 37 (11) ◽  
pp. 2052-2056 ◽  
Author(s):  
J. D. Moore ◽  
T. J. Lychwick

Increased sea lamprey (Petromyzon marinus) abundance in Green Bay during 1977 is documented utilizing sea lamprey counts and lake trout (Salvelinus namaycush) wounding as methods of measurement. Since lake trout rehabilitation began in 1965, sea lamprey predation has been consistently higher in Green Bay and Northern Lake Michigan than other areas of the lake. It appears that increased sea lamprey predation in Green Bay, above the former high levels, resulted in decreased abundance and increased mortality of lake trout. The increase in lampreys is related to the colonization of the Peshtigo River, Marinette County, Wisconsin.Key words: Green Bay, sea lamprey increases, Peshtigo River, lake trout, increased mortality


1980 ◽  
Vol 37 (11) ◽  
pp. 2074-2080 ◽  
Author(s):  
Bruce L. Swanson ◽  
Donald V. Swedberg

The Gull Island Reef lake trout (Salvelinus namaycush) population was one of the few in Lake Superior that was not annihilated by the combined effects of excessive fishing and sea lamprey (Petromyzon marinus) predation. Following control of the lamprey in the early 1960s, this population of lake trout began a slow but steady increase in the average age and numbers of lake trout. Total annual mortality rates for spawning lake trout were 32% for age VI fish, 48% for ages VII–VIII, and 75% for ages IX and older. These total mortality rates included a 7.3% exploitation rate u, a 20% natural mortality n, and annual lamprey-induced mortalities of 6% for ages V–VI, 24%, for ages VII–VIII, and 56% for ages IX and older fish. The estimated number of lake trout eggs deposited annually on Gull Island Reef from 1964 to 1979 ranged from 3.3 million eggs in 1965 to 28 million eggs in 1979, with a mean of 9 million eggs per year. At present levels of lamprey predation, the estimated egg to spawning fish return rate on Gull Island Reef is 0.18%.Key words: lake trout, sea lamprey, survival, population structure, egg deposition


1994 ◽  
Vol 51 (4) ◽  
pp. 942-945 ◽  
Author(s):  
A. L. Jensen

After invasion of the Great Lakes by the parasitic marine sea lamprey (Petromyzon marinus), lake trout (Salvelinus namaycush) populations crashed, but there remains some uncertainty concerning the relative importance of sea lamprey predation and harvesting in destruction of the fisheries. Some investigators believe overharvest was important; others think that the sea lamprey alone was enough. Simple models of predation assume monophagous predators and do not predict extinction of prey, but Larkin's modification of the Lotka–Volterra model results in extinction under some circumstances. The dynamics of sea lamprey predation on lake trout were investigated using Larkin's model, and crude estimates of the model parameters indicate that extinction is a likely outcome with or without a fishery.


1986 ◽  
Vol 43 (12) ◽  
pp. 2528-2531 ◽  
Author(s):  
William D. Swink ◽  
Lee H. Hanson

We tested the hypothesis that the better survival of the Seneca Lake strain of lake trout (Salvelinus namaycush) in Lake Ontario resulted from their greater resistance than other stocked strains to sea lamprey (Petromyzon marinus) predation. No significant difference was found in the survival of Marquette and Seneca Lake strains of Lake trout subjected to single sea lamprey attacks in the laboratory. Of 85 Marquette strain lake trout, 44% died as a direct result of sea lamprey predation, 20% died of undetermined causes, and 36% survived; for 90 lake trout of the Seneca Lake strain, the respective percentages were 39, 21, and 40. The location of sea lamprey attachment on the lake trout was not a factor in mortality, which was significantly higher at water temperatures of 15.6–17.8 °C than at 0.6–15.6 °C. Our study suggested that the seemingly greater survival rate of Seneca Lake fish in Lake Ontario probably resulted from differences in behavior or environmental preferences that decreased their exposure to sea lamprey attacks.


Sign in / Sign up

Export Citation Format

Share Document