Latitudinal Differences in Energy Allocation and Use During the Freshwater Migrations of American Shad (Alosa sapidissima) and Their Life History Consequences

1981 ◽  
Vol 38 (7) ◽  
pp. 806-820 ◽  
Author(s):  
B. D. Glebe ◽  
W. C. Leggett

We studied the relationships between tissue dynamics and bioenergetics of the anadromous American shad (Alosa sapidissima) homing to the St. Johns (Fla.), York (Va.), and Connecticut (Conn.) Rivers and the life history characteristics of these populations. Shad in the three populations studied differed in the degree of development of the gonads at river entry, in the absolute and relative energy allocation to reproductive products vs. migration, and in the extent of total energy depletion during the migration. St. Johns River fish consumed 70–80% of their total energy reserves to reach the spawning grounds and spawn. In this population all shad die following spawning. York River shad consumed ~30% and Connecticut River shad 40–60% of their energy reserves to migrate to the spawning grounds, spawn, and return to the sea. In these populations 25 and 35%, respectively, of the spawning adults survive to spawn again. The principal determinants of energy use were migration distance and river gradient. We rejected the hypothesis that the latitudinal cline in adult survival results from differences in energy use during migration. We concluded that interpopulation differences in energy allocation to migration vs. reproduction are a consequence, rather than a cause, of the different life history strategies exhibited by populations of shad over its Atlantic Coast range. A similar pattern is apparent in other anadromous species: obligate semelparous species use > 70% of their energy reserves to reach the spawning areas and spawn; iteroparous species allocate more energy to postreproductive reserves at the expense of reproductive products thereby ensuring a successful return migration to the sea. Freshwater swimming speeds also appear to differ in a consistent way between semelparous and iteroparous species. Semelparous species swim at close to maximum sustained speed thereby minimizing the duration of the migration. Iteroparous species swim at speeds yielding near optimum energy efficiency (J∙kg−1∙km−1) thereby minimizing the energy cost of migraiton.Key words: American shad, (Alosa sapidissima); migration, bioenergetics, life history tactics, latitudinal clines, swimming speeds, energy allocation, anadromy

1999 ◽  
Vol 56 (7) ◽  
pp. 1159-1171 ◽  
Author(s):  
Jill BK Leonard ◽  
Stephen D McCormick

We examined total and tissue-specific energy content of upstream-migrating American shad (Alosa sapidissima) in the Connecticut River. Total energy depletion over the course of the 228-km migration ranged from 35 to 60%. The approximate contributions of different tissues to energy use during migration were white muscle 57%, subdermal fat 27%, red muscle 8%, viscera 6%, and liver 2%. American shad preferentially use energy stores in the skin and its subdermal fat layer (depleted by 63%) while sparing red muscle protein. Both lipid and protein were used as energy sources throughout migration, although lipids were depleted to a greater extent (e.g., white muscle lipid decreased 48% and protein 30%). Large fish expended 2-21% more energy during migration than small fish. Migrating to upriver sites (198-228 km) is 50-100% more energetically expensive than to lower river sections for females. This suggests that upriver range expansion may be limited by females in that they may have reached a threshold level of energy expenditure in this upriver area. American shad may possess physiological mechanisms for tissue-specific energy use allowing maintenance of critical tissues necessary for postspawning survival.


2017 ◽  
Vol 86 (1) ◽  
pp. 49-67
Author(s):  
Sushree Mohan ◽  
Sampa Banerjee ◽  
Soujita Pramanik ◽  
Soumyajit Banerjee ◽  
Goutam K. Saha ◽  
...  

AbstractEnergy reserves in mosquitoes are an indicator of fitness, linking larval effort in resource acquisition with adult survival and fecundity. In other words, life history strategies and disease transmission potential can be related to the amount of energy reserves. The energy reserves of four mosquitoes –Aedes aegypti, Aedes albopictus, Armigeres subalbatusandCulex quinquefasciatus(Diptera: Culicidae) – were calculated to justify species-specific differences in their life history strategies. Following repeated sampling of pupae from the respective larval habitats, the glycogen, sugar and lipid contents of individual mosquitoes were assessed and corroborated with pupal weight and adult wing length. Discriminant function analysis was used to acquire an initial reflection of the differences of the parameters among the sex and species of the mosquitoes considered in the study. Using logistic regression and ANOVA, the effects of species and sex as contributors to variations in energy reserves could be established. The results indicated that for all the mosquitoes, sex-specific differences were prominent with reference to the energy reserves. Species-specific differences in energy reserves reflect differences in resource acquisition and assimilation in the tissues, and thus the differences in the life history strategies of these four species.


2019 ◽  
Author(s):  
Gretchen F. Wagner ◽  
Emeline Mourocq ◽  
Michael Griesser

Biparental care systems are a valuable model to examine conflict, cooperation, and coordination between unrelated individuals, as the product of the interactions between the parents influences the fitness of both individuals. A common experimental technique for testing coordinated responses to changes in the costs of parental care is to temporarily handicap one parent, inducing a higher cost of providing care. However, dissimilarity in experimental designs of these studies has hindered interspecific comparisons of the patterns of cost distribution between parents and offspring. Here we apply a comparative experimental approach by handicapping a parent at nests of five bird species using the same experimental treatment. In some species, a decrease in care by a handicapped parent was compensated by its partner, while in others the increased costs of care were shunted to the offspring. Parental responses to an increased cost of care primarily depended on the total duration of care that offspring require. However, life history pace (i.e., adult survival and fecundity) did not influence parental decisions when faced with a higher cost of caring. Our study highlights that a greater attention to intergenerational trade-offs is warranted, particularly in species with a large burden of parental care. Moreover, we demonstrate that parental care decisions may be weighed more against physiological workload constraints than against future prospects of reproduction, supporting evidence that avian species may devote comparable amounts of energy into survival, regardless of life history strategy.


2006 ◽  
Vol 84 (1) ◽  
pp. 143-150 ◽  
Author(s):  
Stephen P. Bonser ◽  
Lonnie W. Aarssen

Generalisations of life histories in plants are often framed in terms of allocation to reproduction. For example, relative allocation to reproduction is commonly found to be higher in semelparous than in iteroparous plant species. However, the association between vegetative traits and life history has been largely unexplored. In higher plants, reproductive and vegetative function can be measured in terms of meristem allocation. Under this approach, two vegetative traits (apical dominance (the suppression of axillary meristem development) and branching intensity (the commitment of axillary meristems to branches)) can be measured as well as one reproductive trait (reproductive effort). We used phylogenetically independent contrasts to compare reproductive and vegetative function in annual semelparous and perennial iteroparous species. Twenty congeneric species pairs (each species pair represented by one semelparous and one iteroparous species) across nine families were selected based on availability of herbarium specimens. Semelparous life-history evolution was associated with higher reproductive effort. Conversely, iteroparous life-history evolution was associated with higher apical dominance. Branching intensity was not associated with life history. An evolutionary association between life history and apical dominance but not branching intensity suggests a complex relationship between allocation to vegetative traits and the evolution of plant strategies across environments.


1993 ◽  
Vol 50 (10) ◽  
pp. 2185-2191 ◽  
Author(s):  
Gary K. Meffe ◽  
Franklin F. Snelson Jr.

In animals, strategies of energy allocation among growth, maintenance and reproduction can be significantly altered by lipid storage. Poeciliid (livebearing) fishes store energy in late summer and fall for overwintering and first reproduction in spring, but details of energy use in reproduction are lacking. We conducted a laboratory experiment on the eastern mosquitofish (Gambusia holbrooki) and the sailfin molly (Poecilia latipinna) to document changes in lipid content in both the ovary and soma during development of a brood. In females of both species, ovarian lipid content was highest early in embryogeny and then declined; adult somatic lipids increased (were replenished) during embryonic development in mosquitofish, but declined in mollies. Larger clutches sequestered a larger share of body lipids in both species, possibly indicating energetic limits to reproduction. Finally, growth rate was positively correlated with somatic lipid content in both species, indicating among-individual differences in metabolic efficiency or feeding efficiency rather than a trade-off between growth and energy storage.


Author(s):  
José A. Camacho ◽  
Lucas da Silva Almeida ◽  
Mercedes Rodríguez ◽  
Jesús Molina

AbstractIn order to adequately assess energy policies and set clear objectives, a key preliminary step is to know the energy use patterns of the different countries. This paper estimates the evolution of the total energy use over the period 1995–2015 in four European Union (EU) countries, the Czech Republic, Hungary, Italy, and Spain, representative of two different energy patterns, the “Southern” one and the “Eastern” one. For doing so, we employ a Multi-Regional Input Output (MRIO) model. In difference with previous studies, in addition to differentiate between domestic and foreign use we distinguish whether this energy is produced domestically or abroad. The results obtained show a certain convergence in energy intensity across the four countries examined because of the radical transformations experienced by the Czech Republic and Hungary. Nonetheless, energy intensities are still substantially higher in Eastern than in Southern countries which confirms that the first group of countries have still a long road to go, especially regarding the incentives that their industries have to use energy efficiently. Taking our decomposition of total energy use, the reductions in total energy use were mainly caused by a high decrease in the importance of the domestic use of energy produced domestically. At the same time, a growing importance of the role played by the energy produced abroad was observed. These trends confirm the great importance of global value chains and the steady internalization of energy use. This methodology could be further applied to other countries.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bruno Simmen ◽  
Luca Morino ◽  
Stéphane Blanc ◽  
Cécile Garcia

AbstractLife history, brain size and energy expenditure scale with body mass in mammals but there is little conclusive evidence for a correlated evolution between life history and energy expenditure (either basal/resting or daily) independent of body mass. We addressed this question by examining the relationship between primate free-living daily energy expenditure (DEE) measured by doubly labeled water method (n = 18 species), life history variables (maximum lifespan, gestation and lactation duration, interbirth interval, litter mass, age at first reproduction), resting metabolic rate (RMR) and brain size. We also analyzed whether the hypometabolic primates of Madagascar (lemurs) make distinct energy allocation tradeoffs compared to other primates (monkeys and apes) with different life history traits and ecological constraints. None of the life-history traits correlated with DEE after controlling for body mass and phylogeny. In contrast, a regression model showed that DEE increased with increasing RMR and decreasing reproductive output (i.e., litter mass/interbirth interval) independent of body mass. Despite their low RMR and smaller brains, lemurs had an average DEE remarkably similar to that of haplorhines. The data suggest that lemurs have evolved energy strategies that maximize energy investment to survive in the unusually harsh and unpredictable environments of Madagascar at the expense of reproduction.


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