Literature DB >> 35135317

Large and exaggerated sexually selected weapons comprise high proportions of metabolically inexpensive exoskeleton.

Jason P Dinh1.   

Abstract

The cost-minimization hypothesis proposes that positive allometry in sexually selected traits can be explained if the proportional energetic maintenance costs of weapons decrease as traits increase in size. Energetic maintenance costs are the costs of maintaining homeostasis. They are slow, persistent energy sinks that are distinct from ephemeral costs of growth. Because some tissues expend more energy on maintenance than others, energetic maintenance costs can be inferred from proportional tissue composition. For example, soft tissues require more energy for maintenance than exoskeleton, so an arthropod claw that is 50% soft tissue and 50% exoskeleton would have higher energetic maintenance costs than one that is 30% soft tissue and 70% exoskeleton. I tested the cost-minimization hypothesis using proportional tissue composition as a proxy for energetic maintenance costs in snapping shrimp (Alpheus heterochaelis and Alpheus estuariensis) and fiddler crabs (Uca pugilator). As predicted, larger weapons comprised proportionally less soft tissue mass and more exoskeleton mass than smaller weapons. Furthermore, I extended cost-minimization to explain trait exaggeration: individuals might exaggerate traits by investing more mass in exoskeleton. As predicted, exoskeleton mass proportional to weapon mass increased as exaggeration increased. These results support and extend the cost-minimization hypothesis to explain positive allometry and weapon exaggeration.

Entities:  

Keywords:  allometry; crustacean; exaggeration; sexual selection; weapons

Mesh:

Year:  2022        PMID: 35135317      PMCID: PMC8826129          DOI: 10.1098/rsbl.2021.0550

Source DB:  PubMed          Journal:  Biol Lett        ISSN: 1744-9561            Impact factor:   3.703


  23 in total

Review 1.  Costs of sexual traits: a mismatch between theoretical considerations and empirical evidence.

Authors:  J S Kotiaho
Journal:  Biol Rev Camb Philos Soc       Date:  2001-08

2.  The allometry of ornaments and weapons.

Authors:  Astrid Kodric-Brown; Richard M Sibly; James H Brown
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-26       Impact factor: 11.205

3.  Snapping Behavior of the Shrimp Alpheus californiensis.

Authors:  R Ritzmann
Journal:  Science       Date:  1973-08-03       Impact factor: 47.728

4.  The hidden cost of sexually selected traits: the metabolic expense of maintaining a sexually selected weapon.

Authors:  Ummat Somjee; H Arthur Woods; Meghan Duell; Christine W Miller
Journal:  Proc Biol Sci       Date:  2018-11-14       Impact factor: 5.349

Review 5.  Why Sexually Selected Weapons Are Not Ornaments.

Authors:  Erin L McCullough; Christine W Miller; Douglas J Emlen
Journal:  Trends Ecol Evol       Date:  2016-07-28       Impact factor: 17.712

Review 6.  Evolutionary Trade-Off between Secondary Sexual Traits and Ejaculates.

Authors:  Leigh W Simmons; Stefan Lüpold; John L Fitzpatrick
Journal:  Trends Ecol Evol       Date:  2017-10-16       Impact factor: 17.712

7.  Parallel Saltational Evolution of Ultrafast Movements in Snapping Shrimp Claws.

Authors:  Tomonari Kaji; Arthur Anker; Christian S Wirkner; A Richard Palmer
Journal:  Curr Biol       Date:  2017-12-28       Impact factor: 10.834

8.  Intraspecific male combat behaviour predicts morphology of cervical vertebrae in ruminant mammals.

Authors:  Abby Vander Linden; Elizabeth R Dumont
Journal:  Proc Biol Sci       Date:  2019-11-13       Impact factor: 5.349

9.  Relative brain size and basal metabolic rate in terrestrial vertebrates.

Authors:  R D Martin
Journal:  Nature       Date:  1981-09-03       Impact factor: 49.962

10.  Metabolic incentives for dishonest signals of strength in the fiddler crab Uca vomeris.

Authors:  Candice L Bywater; Craig R White; Robbie S Wilson
Journal:  J Exp Biol       Date:  2014-06-04       Impact factor: 3.312

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.