Bioenergetics of Stock and Recruitment

1980 ◽  
Vol 37 (6) ◽  
pp. 1012-1024 ◽  
Author(s):  
D. M. Ware

A new concept of recruitment is derived from bioenergetic considerations of life history phenomena. The proposed mechanism has two components, a stock-dependent process where individual reproductive effort is a decreasing function of the abundance of the mature stock, and a density-dependent mortality process which operates during the prerecruit stage. A generalized equation describing these processes yields a family of recruitment curves which vary from being asymptotic to dome-shaped, depending on the parameter values. The theory suggests that species like Atlantic herring (Clupea harengus harengus) which tend to have small density-dependent growth coefficients and which allocate most of their surplus energy to reproduction should have a small terminal body size, a high length at maturity to L∞ ratio, and a nearly asymptotic recruitment curve. By contrast, gadoids follow a different life history strategy and therefore should have a higher L∞ and more convex recruitment function. These consequences are shown to be in accord with observed differences in L∞ and with the graded series of recruitment curves found for a wide range of marine fish stocks. From a more general viewpoint, analysis of the energy dynamics of natural populations suggests that (1) there is a real — as opposed to inferred — limit to growth, L∞, which in many species is probably determined by their reproductive effort; (2) the increase in surplus energy with body size can be linked to the theory of optimal foraging; and (3) the intensity of density-dependent growth, which influences the shape of the recruitment curve, is an increasing function of the generation time of the prey organisms of different species. Thus gadoids tend to have dome-shaped reproduction curves because they feed on slow-maturing prey, which can be overcropped by large year-classes.Key words: stock and recruitment, bioenergetics, optimal foraging, growth, reproduction, life history strategies


1990 ◽  
Vol 68 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Larry D. Marshall

Daily egg production of the moth Parapediasia teterrella declined over the life-span of the female but egg size remained constant. The absence of water resulted in lower fecundity and early mortality. Egg size and lifetime fecundity showed considerable inter-individual variation and large females produced more and larger eggs than their smaller counterparts. Large females expended greater reproductive effort than small females. Hatching success was negatively related to egg size. In spite of this, large females laying large eggs had higher fitness than small females. I postulate that multiple reproductive strategies within a species, resulting from differences in reproductive effort expended, may explain why expected trade-offs in reproductive parameters (e.g., egg size versus egg number) were not found in this species. Furthermore, I argue that the prevalent interpretation of life-history evolution (that body size is the important determining parameter of life-history parameters) may reflect correlation of body size with reproductive effort, and reproductive effort may be more important in determining the nature of trade-offs between reproductive parameters.





2016 ◽  
Vol 113 (52) ◽  
pp. 15030-15035 ◽  
Author(s):  
Anne Maria Eikeset ◽  
Erin S. Dunlop ◽  
Mikko Heino ◽  
Geir Storvik ◽  
Nils C. Stenseth ◽  
...  

The relative roles of density dependence and life history evolution in contributing to rapid fisheries-induced trait changes remain debated. In the 1930s, northeast Arctic cod (Gadus morhua), currently the world’s largest cod stock, experienced a shift from a traditional spawning-ground fishery to an industrial trawl fishery with elevated exploitation in the stock’s feeding grounds. Since then, age and length at maturation have declined dramatically, a trend paralleled in other exploited stocks worldwide. These trends can be explained by demographic truncation of the population’s age structure, phenotypic plasticity in maturation arising through density-dependent growth, fisheries-induced evolution favoring faster-growing or earlier-maturing fish, or a combination of these processes. Here, we use a multitrait eco-evolutionary model to assess the capacity of these processes to reproduce 74 y of historical data on age and length at maturation in northeast Arctic cod, while mimicking the stock’s historical harvesting regime. Our results show that model predictions critically depend on the assumed density dependence of growth: when this is weak, life history evolution might be necessary to prevent stock collapse, whereas when a stronger density dependence estimated from recent data is used, the role of evolution in explaining fisheries-induced trait changes is diminished. Our integrative analysis of density-dependent growth, multitrait evolution, and stock-specific time series data underscores the importance of jointly considering evolutionary and ecological processes, enabling a more comprehensive perspective on empirically observed stock dynamics than previous studies could provide.



1986 ◽  
Vol 43 (1) ◽  
pp. 135-141 ◽  
Author(s):  
Elie Moussalli ◽  
Ray Hilborn

If the life history of a population consists of a sequence of density-dependent stages linked by density-independent survival rates, and if the density-dependent stages take the form of the Beverton–Holt stock and recruitment curve, then a single Beverton–Holt curve will describe the entire life history. The relationship between the parameters of any stage in the life history and the optimal harvest rate and optimal stock size is analyzed. Increasing survival rates will always increase the optimal harvest rate, but may increase or decrease the optimal stock size. Increasing the habitat capacity will increase the optimal stock size and leave the optimal harvest rate unaffected. An example of changing freshwater survival rates by Salmonid Enhancement is shown, as is an example of changing ocean survival rate. As we acquire a better understanding of the determinants of survival and habitat capacity, we should adjust harvest rates and stock size as the environment changes.



2010 ◽  
Vol 88 (9) ◽  
pp. 889-899 ◽  
Author(s):  
F. Stephen Dobson ◽  
Pierre Jouventin

A trade-off between reproduction and survival is one of the most consistent empirical aspects of life-history diversification. One explanation for this interspecific pattern is evolved differences in the balance of allocation to reproduction versus individual maintenance and survival. The same pattern is expected, however, simply as a result of differences among species in body size. We tested these alternatives using original data from 44 species of albatrosses and petrels, long-lived seabirds that breed very slowly. After application of regression techniques to remove the effects of body size and phylogeny, annual reproduction and survival exhibited a significant trade-off. Our measures of reproductive effort also exhibited significant trade-offs with age at maturity, the latter strongly associated with survival. Feeding rate of chicks, success at fledging chicks, and annual chick production were also significantly associated. In conclusion, after removing the effects of body size, we found a significant trade-off of reproduction and survival, in spite of the fact that these long-lived birds lay only one egg at a time. Our examination of the pattern among life-history traits of these slow breeders and their pelagic feeding ecology provide support for the evolutionary explanation of a trade-off of reproduction and survival.



1994 ◽  
Vol 51 (5) ◽  
pp. 1169-1179 ◽  
Author(s):  
G. H. Winters ◽  
J. P. Wheeler

We used length-specific weight (i.e., condition) to evaluate growth success of seven stocks of adult Atlantic herring (Clupea harengus) in the Northwest Atlantic. Condition of adult Atlantic herring showed large annual changes as a consequence of abundance-dependent effects. This contradicts the general conclusion that adult herring growth contains little abundance-dependent variation. The published literature, however, is based mainly on traditional growth estimators such as annual length increments which measure only a marginal fraction of annual production whereas condition reflects the seasonal accumulation and depletion of energy and therefore can provide a reliable index of total annual production. We found that annual changes in condition of adult Atlantic herring were only weakly correlated with traditional length-based growth estimates. We concluded that the weak evidence for abundance-dependent growth of adult herring in the literature is a consequence of inappropriate growth estimators. The implication of this finding is that the acquisition of surplus energy by herring can be abundance dependent whereas annual increases in length may not.





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