98%
921
2 minutes
20
Understanding the factors that shape the timing of life-history switch points (SPs; e.g. hatching, metamorphosis and maturation) is a fundamental question in evolutionary ecology. Previous studies examining this question from a fitness optimization perspective have advanced our understanding of why the timing of life-history transitions may vary across populations and environments. However, in nature we also often observe variability among individuals within populations. Optimization theory, which typically predicts a single optimal SP under physiological and environmental constraints for a given environment, cannot explain this variability. Here, we re-examine the evolution of a single life-history SP between juvenile and adult stages from an Adaptive Dynamics (AD) perspective, which explicitly considers the feedback between the dynamics of population and the evolution of life-history strategy. The AD model, although simple in structure, exhibits a diverse range of evolutionary scenarios depending upon demographic and environmental conditions, including the loss of the juvenile stage, a single optimal SP, alternative optimal SPs depending on the initial phenotype, and sympatric coexistence of two SP phenotypes under disruptive selection. Such predictions are consistent with previous optimization approaches in predicting life-history SP variability across environments and between populations, and in addition they also explain within-population variability by sympatric disruptive selection. Thus, our model can be used as a theoretical tool for understanding life-history variability across environments and, especially, within species in the same environment.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283999 | PMC |
http://dx.doi.org/10.1098/rsif.2018.0371 | DOI Listing |
Biology (Basel)
August 2025
Yazhou Bay Innovation Institute, Hainan Tropical Ocean University, Sanya 572000, China.
Although previous studies have investigated the reproductive (performance and mode) and lifespan traits of parthenogenetic , ploidy level has not been considered. Four parthenogenetic lineages, i.e.
View Article and Find Full Text PDFInt J Parasitol
August 2025
Department of Marine Science, University of Otago, New Zealand.
Large ectoparasitic copepods, nearly as long as the length of their host, are often found on Antarctic fish, yet little is known about their biology. In this study, we investigated the genetic structure and host-parasite relationships in Macrourus whitsoni, a deep-sea fish, and its copepod ectoparasite, Lophoura szidati, using 10,569 biallelic SNPs collected from 38 copepods and 5,009 biallelic SNPs from 35 fish individuals across three populations in the Ross Sea, Antarctica. The Fst, DAPC, and admixture analyses revealed distinct genetic patterns between the two species.
View Article and Find Full Text PDFMath Biosci Eng
May 2025
Department of Mathematics, University of Nebraska-Lincoln, Lincoln, NE, USA.
The fitness of an annual plant can be thought of as how much fruit is produced by the end of its growing season. Working under the assumption that annual plants grow to maximize fitness, we use optimal control theory to understand this process. We introduce a model for resource allocation in annual plants that extends classical work by Iwasa and Roughgarden to a case where both carbohydrates and mineral nutrients are allocated to shoots, roots, and fruits.
View Article and Find Full Text PDFJ Theor Biol
September 2025
Department of Advanced Transdisciplinary Science, Hokkaido University, Sapporo, Hokkaido, Japan.
In many butterfly species, males emerge earlier than females as part of a strategy to maximize male reproductive success. Although behavioral ecological studies using mathematical models have been conducted to explain this phenomenon, certain emergence patterns remain unexplained. In the butterfly species Fabriciana nerippe, some males emerge at the same time as females, in addition to males that emerge earlier than the females.
View Article and Find Full Text PDFInsects
May 2025
State Key Laboratory of Cotton Bio-Breeding and Integrated Utilization, Institute of Cotton Research, Chinese Academy of Agricultural Sciences, Anyang 455000, China.
Gynopara is a specific winged type in the life history of . As a key reproduction mode between parthenogenesis and sexual reproduction, it lays sexual females in late autumn. However, little is known about gynoparae because of its rare presence in the wild and the lack of its detailed descriptions.
View Article and Find Full Text PDF