scholarly journals Environmental Influence on Life-History Traits in Male Squid Uroteuthis Edulis With Alternative Reproductive Tactics

2021 ◽  
Author(s):  
Yumeng Pang ◽  
Chih-Shin Chen ◽  
Tomohiko Kawamura ◽  
Yoko Iwata
Keyword(s):  
Life History ◽  
Body Size ◽  
Growth Rates ◽  
Life History Traits ◽  
Environmental Influence ◽  
Life Stage ◽  
Energy Allocation ◽  
Alternative Reproductive Tactics ◽  
Reproductive Tactics ◽  
Somatic Energy

Abstract Squid are characterized by flexible life-history traits (LHTs) that change in response to changing oceanic parameters. Male alternative reproductive tactics (ARTs), characterized by large-sized ‘consorts’ versus small-sized ‘sneakers’, are commonly observed in loliginid species. This study reports on LHTs flexibility in male squids displaying ARTs. LHTs of consorts and sneakers in Uroteuthis edulis, including body size, age, growth rate and gonado-somatic energy allocation, were compared among seasonal and geographical groups from Japan and Taiwan. The ratio of consorts to sneakers was highest in the group spawning in the ‘Japan-warm’ season (June-November), followed by that of the ‘Japan-cold’ season (December-May), and lowest in Taiwan (spring and autumn). LHTs were compared among cohorts separated by hatching season and catch location (Jwarm, Jcold and Taiwan cohorts). Mean body size of consorts showed no difference among cohorts, although Taiwan consorts were relatively younger than Japan consorts. Mean size and age of sneakers decreased with increased water temperature at hatching. Growth rates of consorts and sneakers were slightly different among cohorts, in accordance with differences of statolith increment widths during their early life stage (50-150 d). Growth rates of both consorts and sneakers were highest in the Taiwan cohort, followed by the Jwarm cohort, with the Jcold cohort lowest. Sneakers invested more both in mantle and gonadal weights than consorts in all cohorts. Gonado-somatic energy allocation patterns of consorts and sneakers were consistent at different temperatures. LHTs of U. edulis consorts and sneakers were strongly influenced by temperature, with higher flexibility in sneakers than consorts.

scholarly journals The energy allocation trade-offs underlying life history traits in hypometabolic strepsirhines and other primates

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bruno Simmen ◽  
Luca Morino ◽  
Stéphane Blanc ◽  
Cécile Garcia
Keyword(s):  
Life History ◽  
Energy Expenditure ◽  
Body Mass ◽  
Life History Traits ◽  
Brain Size ◽  
Energy Allocation ◽  
Interbirth Interval ◽  
Energy Investment ◽  
Litter Mass ◽  
Trade Offs

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.

Differential effects on life history traits and body size of two anuran species inhabiting an environment related to fluorite mine

2018 ◽  
Vol 93 ◽  
pp. 36-44 ◽  
Author(s):  
Manuel A. Otero ◽  
Favio E. Pollo ◽  
Pablo R. Grenat ◽  
Nancy E. Salas ◽  
Adolfo L. Martino
Keyword(s):  
Life History ◽  
Body Size ◽  
Life History Traits ◽  
Differential Effects ◽  
Anuran Species

scholarly journals Genetic correlations across genetically determined and developmentally plastic alternative reproductive tactics

2019 ◽  
Author(s):  
Jessica K. Abbott ◽  
Oscar Rios-Cardenas ◽  
Molly Morris
Keyword(s):  
Body Size ◽  
Genetic Correlation ◽  
Genetic Correlations ◽  
Phenotypic Expression ◽  
Alternative Reproductive Tactics ◽  
Phenotypic Trait ◽  
Sexual Antagonism ◽  
Reproductive Tactics ◽  
Genetic Conflict ◽  
Genetically Determined

AbstractAlternative reproductive tactics occur when individuals of the same sex have a suite of morphological and/or behavioural traits that allow them to pursue different reproductive strategies. A common pattern is e.g. the existence of “courter” and “sneaker” tactics within males. We have previously argued that alternative reproductive tactics should be subject to genetic conflict over the phenotypic expression of traits, similar to sexual antagonism. In this process, which we called intra-locus tactical conflict, genetically determined tactics experience conflicting selection on a shared phenotypic trait, such as body size, but a positive genetic correlation between tactics in body size prevents either tactic from reaching its optimum. Recently, other authors have attempted to extend this idea to developmentally plastic alternative reproductive tactics, with mixed results. However, it is not clear whether we should expect intra-locus tactical conflict in developmentally plastic tactics or not. We have therefore run a series of simulation models investigating under what conditions we should expect to see positive estimates of the inter-tactical genetic correlation, since a positive genetic correlation is a prerequisite for the existence of intra-locus tactical conflict. We found that for autosomal, X-linked, and Y-linked genetically-determined tactics, estimated inter-tactical genetic correlations were generally high. However, for developmentally plastic tactics, the genetic correlation depends on the properties of the switching threshold between tactics. If it is fixed, then estimated genetic correlations are positive, but if there is genetic variation in the switch-point, then any sign and magnitude of estimated genetic correlation is possible, even for highly heritable traits where the true underlying correlation is perfect. This means that caution should be used when investigating genetic constraints in plastic phenotypes.

scholarly journals Life history and habitat do not mediate temporal changes in body size due to climate warming in rodents

PeerJ ◽  
2020 ◽  
Vol 8 ◽  
pp. e9792
Author(s):  
Aluwani Nengovhela ◽  
Christiane Denys ◽  
Peter J. Taylor
Keyword(s):  
Life History ◽  
Body Size ◽  
Climate Warming ◽  
Life History Traits ◽  
Vegetation Type ◽  
Reproductive Rate ◽  
Temporal Changes ◽  
Temporal Response ◽  
Extrinsic Factors ◽  
African Species

Temporal changes in body size have been documented in a number of vertebrate species, with different contested drivers being suggested to explain these changes. Among these are climate warming, resource availability, competition, predation risk, human population density, island effects and others. Both life history traits (intrinsic factors such as lifespan and reproductive rate) and habitat (extrinsic factors such as vegetation type, latitude and elevation) are expected to mediate the existence of a significant temporal response of body size to climate warming but neither have been widely investigated. Using examples of rodents, we predicted that both life history traits and habitat might explain the probability of temporal response using two tests of this hypothesis. Firstly, taking advantage of new data from museum collections spanning the last 106 years, we investigated geographical and temporal variation in cranial size (a proxy for body size) in six African rodent species of two murid subfamilies (Murinae and Gerbillinae) of varying life history, degree of commensality, range size, and habitat. Two species, the commensal Mastomys natalensis, and the non-commensal Otomys unisulcatus showed significant temporal changes in body size, with the former increasing and the latter decreasing, in relation with climate warming. Commensalism could explain the increase in size with time due to steadily increasing food availability through increased agricultural production. Apart from this, we found no general life history or habitat predictors of a temporal response in African rodents. Secondly, in order to further test this hypothesis, we incorporated our data into a meta-analysis based on published literature on temporal responses in rodents, resulting in a combined dataset for 50 species from seven families worldwide; among these, 29 species showed no significant change, eight showed a significant increase in size, and 13 showed a decline in size. Using a binomial logistic regression model for these metadata, we found that none of our chosen life history or habitat predictors could significantly explain the probability of a temporal response to climate warming, reinforcing our conclusion based on the more detailed data from the six African species.

Life history and environmental influences on population dynamics in sockeye salmon

2014 ◽  
Vol 71 (8) ◽  
pp. 1198-1208 ◽  
Author(s):  
Douglas C. Braun ◽  
John D. Reynolds
Keyword(s):  
Population Dynamics ◽  
Life History ◽  
Population Growth ◽  
Growth Rates ◽  
Environmental Conditions ◽  
Sockeye Salmon ◽  
Life History Traits ◽  
Relative Importance ◽  
Population Growth Rates ◽  
Habitat Variables

Understanding linkages among life history traits, the environment, and population dynamics is a central goal in ecology. We compared 15 populations of sockeye salmon (Oncorhynchus nerka) to test general hypotheses for the relative importance of life history traits and environmental conditions in explaining variation in population dynamics. We used life history traits and habitat variables as covariates in mixed-effect Ricker models to evaluate the support for correlates of maximum population growth rates, density dependence, and variability in dynamics among populations. We found dramatic differences in the dynamics of populations that spawn in a small geographical area. These differences among populations were related to variation in habitats but not life history traits. Populations that spawned in deep water had higher and less variable population growth rates, and populations inhabiting streams with larger gravels experienced stronger negative density dependence. These results demonstrate, in these populations, the relative importance of environmental conditions and life histories in explaining population dynamics, which is rarely possible for multiple populations of the same species. Furthermore, they suggest that local habitat variables are important for the assessment of population status, especially when multiple populations with different dynamics are managed as aggregates.

Alternative Reproductive Tactics

2020 ◽  
pp. 429-446
Author(s):  
Shawn Garner ◽  
Bryan Neff
Keyword(s):  
Body Size ◽  
Small Body ◽  
Large Body ◽  
Morphological Differentiation ◽  
Alternative Reproductive Tactics ◽  
Reproductive Tactics ◽  
Aggressive Interactions ◽  
Single Sex ◽  
Female Mimicry ◽  
Mating Opportunities

Alternative reproductive tactics (ARTs) describe variation among individuals of a single sex in the tactics used to obtain mating opportunities. In crustaceans, ARTs have been observed in multiple taxa and take a variety of forms. ARTs are most commonly observed in males and are generally associated with intense competition among males to monopolize access to breeding females. ARTs frequently involve a guard tactic that competes with other males to monopolize access to females, while a second usurper tactic foregos competition with other males and instead obtains mating opportunities through sneaking behavior. Guard and usurper tactics may be expressed conditionally based on a male’s ability to guard a female (e.g. his body size, the abundance of competitors), or may be expressed as discrete phenotypes that can also include morphological differentiation. For example, in Jassa amphipods the guard tactic is associated with large body size and an enlarged “thumb” on the claw that is used in aggressive interactions with other males, while the usurper tactic is associated with small body size and a reduced thumb. The usurper tactic can take two forms in a marine isopod: small males (gamma) use sneaking behavior to avoid competition with large males (alpha), whereas intermediate-sized males (beta) use female mimicry to avoid competition. Overall, ARTs are well-represented in crustaceans, with many opportunities for continued study to better characterize these unique adaptations.

Sexual dimorphism in body size and life‐history traits in a population ofTriturus alpestris alpestris

2004 ◽  
Vol 71 (sup2) ◽  
pp. 117-120 ◽  
Author(s):  
Elena Marzona ◽  
Daniele Seglie ◽  
Cristina Giacoma
Keyword(s):  
Life History ◽  
Body Size ◽  
Sexual Dimorphism ◽  
Life History Traits

scholarly journals Do females preferentially associate with males given a better start in life?

2012 ◽  
Vol 8 (3) ◽  
pp. 362-364 ◽  
Author(s):  
Andrew T. Kahn ◽  
Julianne D. Livingston ◽  
Michael D. Jennions
Keyword(s):  
Life History ◽  
Body Size ◽  
Food Intake ◽  
Compensatory Growth ◽  
Life History Traits ◽  
Adult Life ◽  
Gambusia Holbrooki ◽  
Developmental History ◽  
Restricted Diet ◽  
Adult Body

A poor start in life owing to a restricted diet can have readily detectable detrimental consequences for many adult life-history traits. However, some costs such as smaller adult body size are potentially eliminated when individuals modify their development. For example, male mosquitofish ( Gambusia holbrooki ) that have reduced early food intake undergo compensatory growth and delay maturation so that they eventually mature at the same size as males that develop normally. But do subtle effects of a poor start persist? Specifically, does a male's developmental history affect his subsequent attractiveness to females? Females prefer to associate with larger males but, controlling for body length, we show that females spent less time in association with males that underwent compensatory growth than with males that developed normally.

scholarly journals Determinants of life-history traits in a fish ectoparasite: a hierarchical analysis

Parasitology ◽  
2011 ◽  
Vol 138 (7) ◽  
pp. 848-857 ◽  
Author(s):  
G. LOOT ◽  
N. POULET ◽  
S. BROSSE ◽  
L. TUDESQUE ◽  
F. THOMAS ◽  
...  
Keyword(s):  
Life History ◽  
Body Size ◽  
Egg Size ◽  
Life History Traits ◽  
Abiotic Factors ◽  
Individual Characteristics ◽  
Trade Off ◽  
Individual Fitness ◽  
Parasite Number ◽  
Egg Number

SUMMARYObjective. Unravelling the determinants of parasite life-history traits in natural settings is complex. Here, we deciphered the relationships between biotic, abiotic factors and the variation in 4 life-history traits (body size, egg presence, egg number and egg size) in the fish ectoparasite Tracheliastes polycolpus. We then determined the factors affecting the strength of the trade-off between egg number and egg size. Methods. To do so, we used 4-level (parasite, microhabitat, host and environment) hierarchical models coupled to a field database. Results. Variation in life-history traits was mostly due to individual characteristics measured at the parasite level. At the microhabitat level (fins of fish hosts), parasite number was positively related to body size, egg presence and egg number. Higher parasite number on fins was positively associated with individual parasite fitness. At the host level, host body size was positively related to the individual fitness of the parasite; parasites were bigger and more fecund on bigger hosts. In contrast, factors measured at the environmental level had a weak influence on life-history traits. Finally, a site-dependent trade-off between egg number and egg size existed in this population. Conclusion. Our study illustrates the importance of considering parasite life-history traits in a hierarchical framework to decipher complex links between biotic, abiotic factors and parasite life-history traits.

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