Life History Variations of Anadromous Cisco (Coregonus artedii), Lake Whitefish (C. clupeaformis), and Round Whitefish (Prosopium cylindraceum) Populations of Eastern James–Hudson Bay

1982 ◽  
Vol 39 (7) ◽  
pp. 958-967 ◽  
Author(s):  
Roderick Morin ◽  
Julian J. Dodson ◽  
Geoffrey Power

Differences in life history among three species of anadromous coregonines from La Grande River, James Bay, were significant with lake whitefish (Coregonus clupeaformis) and round whitefish (Prosopium cylindraceum) displaying reproductive patterns more typical of harsh northern environments and characteristic of "K-selection," relative to cisco (Coregonus artedii). Interspecific differences at La Grande River were more apparent than intraspecific differences in life history traits of cisco and lake whitefish over the James–Hudson Bay range. Although cisco exhibit decreasing reproductive effort independent of growth over the North American range, thus conforming to life history theory, both growth and reproductive effort are reduced northwards over their James–Hudson Bay range. The observations suggest that physiological constraints related to the shorter growing season at the northern limit of cisco's coastal Hudson Bay range may overwhelm expected coadapted life history traits. Lake whitefish exhibit reduced reproductive effort independent of variations in growth northwards over their North American and James–Hudson Bay coastal range; this suggests coadaptation of life history traits that permit survival at northern sites.Key words: reproduction, growth, life history theory, anadromous coregonines, James–Hudson Bay

Author(s):  
Jeffrey A. Hutchings

Life histories describe how genotypes schedule their reproductive effort throughout life in response to factors that affect their survival and fecundity. Life histories are solutions that selection has produced to solve the problem of how to persist in a given environment. These solutions differ tremendously within and among species. Some organisms mature within months of attaining life, others within decades; some produce few, large offspring as opposed to numerous, small offspring; some reproduce many times throughout their lives while others die after reproducing just once. The exponential pace of life-history research provides an opportune time to engage and re-engage new generations of students and researchers on the fundamentals and applications of life-history theory. Chapters 1 through 4 describe the fundamentals of life-history theory. Chapters 5 through 8 focus on the evolution of life-history traits. Chapters 9 and 10 summarize how life-history theory and prediction has been applied within the contexts of conservation and sustainable exploitation. This primer offers an effective means of rendering the topic accessible to readers from a broad range of academic experience and research expertise.


1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold

Recently, Zammuto (R. M. Zammuto. 1986. Can. J. Zool. 64: 2739–2749) suggested that North American game birds exhibited survival–fecundity trade-offs consistent with the "cost of reproduction" hypothesis. However, there were four serious problems with the data and the analyses that Zammuto used: (i) the species chosen for analysis ("game birds") showed little taxonomic or ecological uniformity, (ii) the measures of future reproductive value (maximum longevity) were severely biased by unequal sample sizes of band recoveries, (iii) the measures of current reproductive effort (clutch sizes) were inappropriate given that most of the birds analyzed produce self-feeding precocial offspring, and (iv) the statistical units used in the majority of analyses (species) were not statistically independent with respect to higher level taxonomy. After correcting these problems, I found little evidence of survival–fecundity trade-offs among precocial game birds, and I attribute most of the explainable variation in life-history traits of these birds to allometry, phylogeny, and geography.


Science ◽  
1931 ◽  
Vol 73 (1901) ◽  
pp. 620-621
Author(s):  
Emery Westervelt Dennis

2021 ◽  
pp. 1-7
Author(s):  
Ken S. Toyama ◽  
Christopher K. Boccia

Abstract Opposing life history strategies are a common result of the different ecological settings experienced by insular and continental species. Here we present a comprehensive compilation of data on sexual size dimorphism (SSD) and life history traits of Microlophus, a genus of lizards distributed in western South America and the Galápagos Islands, and test for differences between insular and continental species under life history theory expectations. Contrary to our predictions, we found no differences in SSD between localities or evidence that Microlophus follows Rensch’s rule. However, as expected, head dimensions and maturity sizes were significantly larger in insular species while continental species had larger clutches. Our results show that Microlophus exhibits some of the patterns expected from an island-mainland system, but unexplained patterns will only be resolved through future ecological, morphological and behavioural studies integrating both faunas.


1990 ◽  
Vol 47 (2) ◽  
pp. 335-345 ◽  
Author(s):  
Yvan Lambert ◽  
Julian J. Dodson

We tested the hypothesis that differences in the cost of freshwater migration are responsible for the different reproductive patterns exhibited by the Eastmain River (James Bay) populations of anadromous cisco and lake whitefish, as predicted by species-specific migration costs that result in interspecific differences in energy allocation to growth, survival, and reproduction. In the Eastmain River, cisco spawn at a younger age and a smaller size, have a shorter life span and show a higher fecundity and a higher mortality than lake whitefish. Assuming that the two populations are stable (being only lightly exploited), the two species spawn at an age that maximizes their lifetime fecundity. Either juvenile (between three and age at maturity) and/or adult mortality is of major importance in moulding the observed age at maturity but adult mortality may play a predominant role. Adult mortality is associated with migration, an obligatory cost representing a major proportion of the energy loss experienced by reproductive individuals. The difference in the energy cost of migration between the two species suggests that migration may play a predominant role in producing the different reproductive patterns of cisco and lake whitefish in the Eastmain River and that within the physiological and size constraints of each species, these patterns represent optimal adaptations maximizing fitness.


2018 ◽  
Vol 8 (5) ◽  
pp. 2632-2644 ◽  
Author(s):  
Paul G. Harnik ◽  
Hafiz Maherali ◽  
Joshua H. Miller ◽  
Paul S. Manos

1985 ◽  
Vol 22 (4) ◽  
pp. 553-566 ◽  
Author(s):  
K. L. Buchan ◽  
W. R. A. Baragar

The komatiitic basalts of the Ottawa Islands in eastern Hudson Bay are on strike with and believed to form a continuation of similar units of the Cape Smith Belt 150 km to the northeast. Units sampled in the Ottawa Islands all dip gently to the west and hence are not suitable for an internal fold test of their age of magnetization. However, before correcting for the tilt of the lavas, the dominant magnetization direction (D = 207.6°, I = 61.9°, k = 168, α95 = 3.7°) does not differ significantly from the uncorrected magnetization direction reported from the steeply dipping, northwest-facing units at Cape Smith (D = 218°, I = 60°, k = 47, α95 = 4°). This negative fold test suggests that the remanence at both locations was acquired after folding. Comparison with the North American Precambrian apparent polar wander path implies that overprinting is related to the Hudsonian Orogeny.A second stable magnetization directed to the west with a shallow inclination is superimposed on the dominant component at a number of sampling sites. Its direction is poorly defined and no fold test is possible. However, magnetic evidence suggests that this component was probably acquired as an overprint after the dominant magnetization, perhaps during a mild reheating associated with the Elsonian Orogeny.


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