Sexually selected traits and life history traits of larger and smaller males of the horned flour beetle Gnatocerus cornutus

2021 ◽  
Author(s):  
Katsuya Kiyose ◽  
Yasukazu Okada ◽  
Masako Katsuki ◽  
Yû Suzaki ◽  
Kensuke Okada
2021 ◽  
Author(s):  
Martin David Garlovsky ◽  
Luke Holman ◽  
Andrew L Brooks ◽  
Rhonda R Snook

Sexual selection and sexual conflict are expected to affect all aspects of the phenotype, not only traits that are directly involved in reproduction. Here, we show coordinated evolution of multiple physiological and life history traits in response to long-term experimental manipulation of the mating system in populations of Drosophila pseudoobscura. Development time was extended under polyandry relative to monogamy in both sexes, potentially due to higher investment in traits linked to sexual selection and sexual conflict. Individuals (especially males) evolving under polyandry had higher metabolic rates and locomotor activity than those evolving under monogamy. Polyandry individuals also invested more in metabolites associated with increased endurance capacity and efficient energy metabolism and regulation, namely lipid and glycogen. Finally, polyandry males were less desiccation- and starvation-resistant than monogamy males, suggesting trade-offs between resistance and sexually selected traits. Our results provide experimental evidence that mating systems can impose selection that influences the evolution of non-sexual phenotypes such as development, activity, metabolism, and nutrient homeostasis.


2017 ◽  
Vol 26 (1) ◽  
pp. 142-153 ◽  
Author(s):  
Inon Scharf ◽  
Keren-Or Wertheimer ◽  
Joy Lim Xin ◽  
Tomer Gilad ◽  
Inna Goldenberg ◽  
...  

2014 ◽  
Vol 33 (3) ◽  
pp. 812-819 ◽  
Author(s):  
Rickey D. Cothran ◽  
Aaron B. Stoler ◽  
Rick A. Relyea

2020 ◽  
Vol 650 ◽  
pp. 7-18 ◽  
Author(s):  
HW Fennie ◽  
S Sponaugle ◽  
EA Daly ◽  
RD Brodeur

Predation is a major source of mortality in the early life stages of fishes and a driving force in shaping fish populations. Theoretical, modeling, and laboratory studies have generated hypotheses that larval fish size, age, growth rate, and development rate affect their susceptibility to predation. Empirical data on predator selection in the wild are challenging to obtain, and most selective mortality studies must repeatedly sample populations of survivors to indirectly examine survivorship. While valuable on a population scale, these approaches can obscure selection by particular predators. In May 2018, along the coast of Washington, USA, we simultaneously collected juvenile quillback rockfish Sebastes maliger from both the environment and the stomachs of juvenile coho salmon Oncorhynchus kisutch. We used otolith microstructure analysis to examine whether juvenile coho salmon were age-, size-, and/or growth-selective predators of juvenile quillback rockfish. Our results indicate that juvenile rockfish consumed by salmon were significantly smaller, slower growing at capture, and younger than surviving (unconsumed) juvenile rockfish, providing direct evidence that juvenile coho salmon are selective predators on juvenile quillback rockfish. These differences in early life history traits between consumed and surviving rockfish are related to timing of parturition and the environmental conditions larval rockfish experienced, suggesting that maternal effects may substantially influence survival at this stage. Our results demonstrate that variability in timing of parturition and sea surface temperature leads to tradeoffs in early life history traits between growth in the larval stage and survival when encountering predators in the pelagic juvenile stage.


2020 ◽  
Vol 27 (4) ◽  
pp. 195-200
Author(s):  
Ufuk Bülbül ◽  
Halime Koç ◽  
Yasemin Odabaş ◽  
Ali İhsan Eroğlu ◽  
Muammer Kurnaz ◽  
...  

Age structure of the eastern spadefoot toad, Pelobates syriacus from the Kızılırmak Delta (Turkey) were assessed using phalangeal skeletochronology. Snout-vent length (SVL) ranged from 42.05 to 86.63 mm in males and 34.03 to 53.27 mm in females. Age of adults ranged from 2 to 8 years in males and 3 to 5 years in females. For both sexes, SVL was significantly correlated with age. Males and females of the toads reached maturity at 2 years of age.


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