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Sexual dimorphism in subterranean amphipod crustaceans covaries with subterranean habitat type.
Premate, Ester; Fiser, Ziga; Biró, Anna; Copilas-Ciocianu, Denis; Fromhage, Lutz; Jennions, Michael; Borko, Spela; Herczeg, Gábor; Balázs, Gergely; Kralj-Fiser, Simona; Fiser, Cene.
Afiliación
  • Premate E; Department of Biology, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia.
  • Fiser Z; Department of Biology, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia.
  • Biró A; Doctoral School of Biology, Institute of Biology, ELTE-Eötvös Loránd University, Budapest, Hungary.
  • Copilas-Ciocianu D; ELKH-ELTE-MTM Integrative Ecology Research Group, Budapest, Hungary.
  • Fromhage L; Department of Systematic Zoology and Ecology, Institute of Biology, ELTE-Eötvös Loránd University, Budapest, Hungary.
  • Jennions M; Laboratory of Evolutionary Ecology of Hydrobionts, Nature Research Centre, Vilnius, Lithuania.
  • Borko S; Department of Biological and Environmental Science, University of Jyvaskyla, Jyväskylä, Finland.
  • Herczeg G; Division of Ecology & Evolution, Research School of Biology, The Australian National University, Acton, Canberra, ACT, Australia.
  • Balázs G; Stellenbosch Institute for Advanced Study (STIAS), Wallenberg Centre, Stellenbosch, South Africa.
  • Kralj-Fiser S; Department of Biology, Biotechnical Faculty, University of Ljubljana, Ljubljana, Slovenia.
  • Fiser C; ELKH-ELTE-MTM Integrative Ecology Research Group, Budapest, Hungary.
J Evol Biol ; 37(5): 487-500, 2024 May 06.
Article en En | MEDLINE | ID: mdl-38483086
ABSTRACT
Sexual dimorphism can evolve in response to sex-specific selection pressures that vary across habitats. We studied sexual differences in subterranean amphipods Niphargus living in shallow subterranean habitats (close to the surface), cave streams (intermediate), and cave lakes (deepest and most isolated). These three habitats differ because at greater depths there is lower food availability, reduced predation, and weaker seasonality. Additionally, species near the surface have a near-even adult sex ratio (ASR), whereas species from cave lakes have a female-biased ASR. We hypothesized (a) a decrease in sexual dimorphism from shallow subterranean habitats to cave lake species because of weaker sexual selection derived from changes in the ASR and (b) an increase in female body size in cave lakes because of stronger fecundity selection on account of oligotrophy, reduced predation, and weaker seasonality. We measured body size and two sexually dimorphic abdominal appendages for all 31 species and several behaviours related to male competition (activity, risk-taking, exploration) for 12 species. Species with an equal ASR that live close to the surface exhibited sexual dimorphism in all three morphological traits, but not in behaviour. The body size of females increased from the surface to cave lakes, but no such trend was observed in males. In cave lake species, males and females differed neither morphologically nor behaviourally. Our results are consistent with the possibility that sexual and fecundity selection covary across the three habitats, which indirectly and directly, respectively, shape the degree of sexual dimorphism in Niphargus species.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Caracteres Sexuales / Ecosistema / Anfípodos Límite: Animals Idioma: En Revista: J Evol Biol Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Eslovenia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Caracteres Sexuales / Ecosistema / Anfípodos Límite: Animals Idioma: En Revista: J Evol Biol Asunto de la revista: BIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Eslovenia