Intraspecific variation in reproductive effort by female Parapediasia teterrella (Lepidoptera: Pyralidae) and its relation to body size

1990 ◽  
Vol 68 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Larry D. Marshall
Keyword(s):  
Life History ◽  
Body Size ◽  
Egg Production ◽  
Egg Size ◽  
Reproductive Effort ◽  
Life History Evolution ◽  
Reproductive Parameters ◽  
Trade Offs ◽  
Egg Number ◽  
Lepidoptera Pyralidae

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.

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.

The reproductive effort of Lepeophtheirus pectoralis (Copepoda: Caligidae): insights into the egg production strategy of parasitic copepods

Parasitology ◽  
2015 ◽  
Vol 143 (1) ◽  
pp. 87-96 ◽  
Author(s):  
D. G. FRADE ◽  
M. J. SANTOS ◽  
F. I. CAVALEIRO
Keyword(s):  
Egg Production ◽  
Egg Size ◽  
Reproductive Effort ◽  
Parasitic Copepods ◽  
Egg Number ◽  
Production Strategy ◽  
European Flounder ◽  
Fish Hosts ◽  
First Time ◽  
The Relationship

SUMMARYThe reproductive effort of Lepeophtheirus pectoralis (Müller O. F., 1776), a caligid copepod, which is commonly found infecting the European flounder, Platichthys flesus (Linnaeus, 1758), is studied in detail for the first time. Seasonal variation in body dimensions and reproductive effort are analysed. Data for 120 ovigerous females, 30 from each season of the year, were considered in the analyses. Females were larger and produced a larger number of smaller eggs in winter, than during the summer. The relationship between egg number and egg size is similar to that recorded for other copepods exploiting fish hosts. Much of the recorded variation was also similar to that reported for a copepod parasitic on an invertebrate host, which suggests the possibility of a general trend in copepod reproduction. Overall, our results provide further support for the hypothesis that there is an alternation of summer and winter generations.

Reproductive Effort and Costs

2021 ◽  
pp. 59-74
Author(s):  
Jeffrey A. Hutchings
Keyword(s):  
Life History ◽  
Reproductive Success ◽  
Total Energy ◽  
Reproductive Effort ◽  
Life History Evolution ◽  
Reproductive Costs ◽  
Positive Outcomes ◽  
Differential Allocation ◽  
Trade Offs ◽  
Potential Benefits

Predictions about life-history evolution are intellectually bereft without a consideration of trade-offs. Benefits derived from making one life-history ‘decision’ are made at a cost of not realizing potential benefits associated with alternative decisions. These trade-offs are the inevitable product of constraints, often driven by an individual’s differential allocation of fixed resources to reproduction versus survival or growth. These allocations prevent multiple positive outcomes from being simultaneously realized. Reproductive effort is the proportion of total energy or resources allocated to all elements of reproduction. Reproductive effort generates reproductive costs. Increases in current reproductive effort reduce future reproductive success by affecting survival, growth, and/or fecundity. The causal mechanisms of these costs can be energetic, ecological, behavioural, or genetic. Evidence for reproductive costs is widespread. Instances where the evidence of costs is equivocal are usually caused by using among-individual correlations to study what is a within-individual phenomenon.

Egg production in adult trematodes: adaptation or constraint?

Parasitology ◽  
1997 ◽  
Vol 114 (2) ◽  
pp. 195-204 ◽  
Author(s):  
R. POULIN
Keyword(s):  
Life History ◽  
Body Size ◽  
Life Histories ◽  
Egg Production ◽  
Egg Size ◽  
Life History Traits ◽  
Sampling Site ◽  
Consistent Difference ◽  
Host Body Mass ◽  
Trematode Parasites

Parasite life-history traits should reflect past environmental and host-related selective pressures acting to produce strategies that maximize transmission success. The evolution of adult body size and egg production in 804 species of trematode parasites was investigated using independent contrasts derived from a phylogeny of trematodes. Contrasts in trematode body size were positively correlated with contrasts in egg size, and almost significantly correlated with contrasts in numbers of uterine eggs. After controlling for body size, no relationship existed between egg size and egg numbers, suggesting that there is no trade-off between the two components of egg production. Average host body mass and latitude of the sampling site did not correlate with either trematode body size or egg size. Contrasts between trematode taxa exploiting ectotherm hosts and their sister taxa exploiting endotherms showed no consistent difference in either body size or egg size. The effect of other variables on trematode life-histories, such as the nature of the habitat in which eggs are released, the site of attachment within the host's body, or the number of hosts involved in the life-cycle, could not be evaluated statistically. The similarity in life-history traits among members of given clades suggests that phylogenetic constraints may have acted to limit or mask any adaptive changes expected from changes in host-related or environmental conditions.

Life History Adaptation in Prey

2018 ◽  
pp. 323-346
Author(s):  
Gary A. Wellborn
Keyword(s):  
Life History ◽  
Life History Theory ◽  
Reproductive Effort ◽  
Life History Evolution ◽  
Reproductive Value ◽  
Offspring Size ◽  
Selective Predation ◽  
Antipredator Defense ◽  
Trade Offs ◽  
History Evolution

Predation is a powerful agent of life history evolution in prey species, as demonstrated in diverse examples in crustaceans. Ubiquitous size- and age-selective predation mediates trade-offs among reproductive effort, survival, and growth, which cause evolution of constitutive and phenotypically plastic shifts in age and size at maturity. In accord with predictions of life history theory, comparative studies demonstrate that contrasting forms of selective predation generate divergent evolutionary changes in age- and size-specific allocation of reproductive effort within populations and species. Predation risk also influences egg and offspring size, and some crustaceans exhibit phenotypic plasticity in offspring size in response to chemical cues of predators. Because age-selective predation impacts the relative benefits of earlier versus later reproductive investment, predation may also shape senescence and life span of crustaceans. Additionally, individual differences in risk-taking behavior, sometimes termed “personalities,” have been examined in several crustaceans, and these may arise through among-individual variation in reproductive value. Finally, in some crustacean groups limb autotomy is a common, but costly, antipredator defense, and life history perspectives on autotomy suggest individuals may balance costs and benefits during predator encounters. Much of our understanding of predation’s role in life history evolution of prey derives from studies of crustaceans, and these organisms continue to be promising avenues to elucidate mechanisms of life history evolution.

The trade-off of reproduction and survival in slow-breeding seabirds

2010 ◽  
Vol 88 (9) ◽  
pp. 889-899 ◽  
Author(s):  
F. Stephen Dobson ◽  
Pierre Jouventin
Keyword(s):  
Life History ◽  
Body Size ◽  
Life History Traits ◽  
Feeding Rate ◽  
Reproductive Effort ◽  
Original Data ◽  
Age At Maturity ◽  
Trade Off ◽  
Trade Offs ◽  
Regression Techniques

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.

Egg size and shape, clutch dynamics, and reproductive effort in European tortoises

1988 ◽  
Vol 66 (7) ◽  
pp. 1527-1536 ◽  
Author(s):  
A. Hailey ◽  
N. S. Loumbourdis
Keyword(s):  
Body Size ◽  
Clutch Size ◽  
Egg Production ◽  
Egg Size ◽  
Reproductive Effort ◽  
Energy Content ◽  
The Body ◽  
Female Reproduction ◽  
Northern Greece ◽  
Clutch Mass

Energetic aspects of female reproduction are described for the tortoises Testudo graeca, Testudo marginata, and Testudo hermanni (three populations of different body size) from northern Greece. Egg width increased with body size in some populations, but smaller individuals produced more elongate eggs, and egg weight was not related to body size. This method for overcoming the constraint of the width of the pelvic canal means that egg width is a poor measure of egg size. Clutch size, clutch mass, and annual egg production varied with body size between populations. Mean relative clutch mass ranged from 4 to 7%, and was highest in the three populations of T. hermanni. All populations laid two or three clutches per year, based on the total number of eggs and large follicles divided by clutch size. Multiple clutches reflect the morphological constraint of packing shelled eggs within the body, rather than energy accumulation during the nesting period. Material for reproduction was stored in growing follicles rather than fat bodies; follicles reached half of their final weight before the animals entered hibernation. Annual reproductive effort as a proportion of body energy content was about 15% in all populations. This is lower than in other reptiles, partly because the carapace accounts for over half of the total ash-free dry weight of the tortoise body.

scholarly journals The physiological costs of reproduction in small mammals

2007 ◽  
Vol 363 (1490) ◽  
pp. 375-398 ◽  
Author(s):  
John R Speakman
Keyword(s):  
Life History ◽  
Small Mammals ◽  
Morphological Changes ◽  
Life History Evolution ◽  
Indirect Costs ◽  
Direct Costs ◽  
Costs Of Reproduction ◽  
Dominant Component ◽  
Trade Offs ◽  
Almost All

Life-history trade-offs between components of fitness arise because reproduction entails both gains and costs. Costs of reproduction can be divided into ecological and physiological costs. The latter have been rarely studied yet are probably a dominant component of the effect. A deeper understanding of life-history evolution will only come about once these physiological costs are better understood. Physiological costs may be direct or indirect. Direct costs include the energy and nutrient demands of the reproductive event, and the morphological changes that are necessary to facilitate achieving these demands. Indirect costs may be optional ‘compensatory costs’ whereby the animal chooses to reduce investment in some other aspect of its physiology to maximize the input of resource to reproduction. Such costs may be distinguished from consequential costs that are an inescapable consequence of the reproductive event. In small mammals, the direct costs of reproduction involve increased energy, protein and calcium demands during pregnancy, but most particularly during lactation. Organ remodelling is necessary to achieve the high demands of lactation and involves growth of the alimentary tract and associated organs such as the liver and pancreas. Compensatory indirect costs include reductions in thermogenesis, immune function and physical activity. Obligatory consequential costs include hyperthermia, bone loss, disruption of sleep patterns and oxidative stress. This is unlikely to be a complete list. Our knowledge of these physiological costs is currently at best described as rudimentary. For some, we do not even know whether they are compensatory or obligatory. For almost all of them, we have no idea of exact mechanisms or how these costs translate into fitness trade-offs.

scholarly journals Life‐history evolution in the anthropocene: effects of increasing nutrients on traits and trade‐offs

2015 ◽  
Vol 8 (7) ◽  
pp. 635-649 ◽  
Author(s):  
Emilie Snell‐Rood ◽  
Rickey Cothran ◽  
Anne Espeset ◽  
Punidan Jeyasingh ◽  
Sarah Hobbie ◽  
...  
Keyword(s):  
Life History ◽  
Life History Evolution ◽  
Trade Offs ◽  
History Evolution
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