Mechanisms of coexistence between native bull trout (Salvelinus confluentus) and non-native lake trout (Salvelinus namaycush): inferences from pattern-oriented modeling

2012 ◽  
Vol 69 (4) ◽  
pp. 755-769 ◽  
Author(s):  
Jake M. Ferguson ◽  
Mark L. Taper ◽  
Christopher S. Guy ◽  
John M. Syslo

Determining the ecological mechanisms that control population abundances is an important issue for the conservation of endangered and threatened species. We examined whether a threatened bull trout ( Salvelinus confluentus ) population could coexist at observed levels with the ecologically similar introduced species, lake trout ( Salvelinus namaycush ), using a pattern-oriented analysis of population dynamics models. We used a large suite of stage- and age-structured models to examine how both competitive and predatory interactions, combined with differing life-history strategies and species vital rates, drove salmonid coexistence patterns. In our models, an ontogenetic shift in juvenile bull trout resource use was the most important factor contributing to the two species coexistence; however, this coexistence occurred with reduced abundances in bull trout that increase the chances of extirpation for the native species. Observed levels of competition were found to have stronger effects than predation on population abundances. We used a pattern-oriented modeling approach to inference; this approach assumes process models that can generate patterns similar to the observed patterns are better supported than those that cannot. This methodology may find wide use on a number of data-limited fishery management and conservation problems.

1993 ◽  
Vol 71 (2) ◽  
pp. 238-247 ◽  
Author(s):  
David B. Donald ◽  
David J. Alger

Indigenous lacustrine populations of bull trout (Salvelinus confluentus) and lake trout (S. namaycush) are spatially separated within the southern part of the zone of distributional overlap (northern Montana, southwestern Alberta, and east-central British Columbia). In this area, lake trout occurred primarily in mountain lakes of 1032–1500 m elevation, while bull trout were found primarily in lakes between 1500 and 2200 m. Introductions of lake trout in the twentieth century and data obtained from beyond the study area indicated that both fishes can establish significant allopatric populations (more than 5% of the catch) in large, deep lakes (>8 ha in area and >8 m deep) over a wide elevation range. We tested the hypothesis that lake trout displace or exclude bull trout from lakes by determining the outcome of introductions of lake trout into two lakes that supported indigenous bull trout. Lake trout were introduced into Bow Lake in 1964, and by 1992 the bull trout population was decimated there and in another lake (Hector) situated 15 km downstream. Thus, lake trout can displace bull trout and may prevent bull trout from becoming established in certain low-elevation lakes. Population age-structure analyses also suggest that lake trout adversely affected bull trout. Bull trout populations in sympatry with lake trout, including the one extirpated from Hector Lake, had few old fish (18% were more than 5 years old; N = 40 fish from three lakes) compared with allopatric populations (49% were more than 5 years old; N = 235 fish from seven lakes). Niche overlap and the potential for competition between the two char species were substantial. In lakes with trophic structure ranging from simple to complex, bull trout and lake trout fed on similar foods and had similar ecological efficiencies (growth rates). Predation by lake trout on bull trout was not documented during the study.


2006 ◽  
Vol 63 (1) ◽  
pp. 63-78 ◽  
Author(s):  
Bruce E Rieman ◽  
James T Peterson ◽  
Deborah L Myers

Invasions of non-native brook trout (Salvelinus fontinalis) have the potential for upstream displacement or elimination of bull trout (Salvelinus confluentus) and other native species already threatened by habitat loss. We summarized the distribution and number of bull trout in samples from 12 streams with and without brook trout in central Idaho and used hierarchical regression analysis to consider whether brook trout have displaced bull trout along gradients of temperature and elevation. Brook trout generally were observed in higher numbers downstream of bull trout. Brook trout presence, number, and both temperature and elevation were important variables explaining the observed distributions and number of bull trout among streams. Our analyses support the hypothesis that brook trout have displaced bull trout, but results were highly variable and stream dependent. Although brook trout appeared to have displaced bull trout to higher elevations or colder temperatures, there was no clear influence on overall number of bull trout. Brook trout probably do influence bull trout populations and facilitate if not cause local extinctions, but threats probably vary strongly with environmental conditions. Bull trout in smaller streams could be more vulnerable than those in larger streams.


2006 ◽  
Vol 63 (5) ◽  
pp. 1157-1171 ◽  
Author(s):  
Eric B Taylor ◽  
A B Costello

Microsatellite DNA variation was assayed among 383 bull trout (Salvelinus confluentus) from 20 Pacific coastal localities from the Skeena River (central British Columbia) to the Olympic Peninsula (western Washington State). An average of 1.7 alleles was resolved per population and heterozygosity averaged 0.35. Twenty-six fish were identified as bull trout × Dolly Varden (Salvelinus malma) hybrids. Population subdivision was substantial (θ = 0.33), but subdivision was higher (θ = 0.46) when interior populations (N = 37) were included, indicating a major genetic distinction between "coastal" and "interior" bull trout. Bull trout populations north of the Squamish River were genetically more similar to interior bull trout than to other more southern coastal populations, suggesting that they had been founded by headwater transfers from interior populations. Individual assignment of bull trout averaged 53.4% correct assignment among populations (range: 12%–95%). Mixture analysis indicated that most fish from the lower Fraser River recreational fishery originated from major nearby tributaries (e.g., Pitt, upper Lillooet, and Chilliwack rivers). Our results substantiate the existence of two major evolutionary lineages of bull trout and highlight the importance of tributary habitats for the persistence of local populations, as well as for those that forage in downstream areas on the lower Fraser River.


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


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Ana I. García-Cervigón ◽  
Pedro F. Quintana-Ascencio ◽  
Adrián Escudero ◽  
Merari E. Ferrer-Cervantes ◽  
Ana M. Sánchez ◽  
...  

AbstractPopulation persistence is strongly determined by climatic variability. Changes in the patterns of climatic events linked to global warming may alter population dynamics, but their effects may be strongly modulated by biotic interactions. Plant populations interact with each other in such a way that responses to climate of a single population may impact the dynamics of the whole community. In this study, we assess how climate variability affects persistence and coexistence of two dominant plant species in a semiarid shrub community on gypsum soils. We use 9 years of demographic data to parameterize demographic models and to simulate population dynamics under different climatic and ecological scenarios. We observe that populations of both coexisting species may respond to common climatic fluctuations both similarly and in idiosyncratic ways, depending on the yearly combination of climatic factors. Biotic interactions (both within and among species) modulate some of their vital rates, but their effects on population dynamics highly depend on climatic fluctuations. Our results indicate that increased levels of climatic variability may alter interspecific relationships. These alterations might potentially affect species coexistence, disrupting competitive hierarchies and ultimately leading to abrupt changes in community composition.


Author(s):  
Alexander Gatch ◽  
Dimitry Gorsky ◽  
Zy Biesinger ◽  
Eric Bruestle ◽  
Kelley Lee ◽  
...  

1997 ◽  
Vol 54 (5) ◽  
pp. 1031-1038
Author(s):  
C A Stow ◽  
L J Jackson ◽  
J F Amrhein

We examined data from 1984 to 1994 for five species of Lake Michigan salmonids to explore the relationship between total PCB concentration and percent lipid. When we compared mean species lipid and PCB values, we found a strong linear correlation. When we compared values among individuals, we found modest positive PCB:lipid associations in brown trout (Salmo trutta), chinook salmon (Oncorhynchus tshawytscha), coho salmon (Oncorhynchus kisutch), and rainbow trout (Oncorhynchus mykiss) collected during spawning, but positive associations were not apparent among nonspawning individuals. Lake trout (Salvelinus namaycush) exhibited no discernible PCB:lipid relationship. Our results are not incompatible with previous observations that contaminants are differentially partitioned into lipids within a fish, but these results do suggest that lipids are not a major factor influencing contaminant uptake.


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


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