Cargando…
Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death
All living organisms must eventually die, though in some cases their death can bring life‐giving opportunities. Few studies, however, have experimentally tested how animals capitalize on conspecific death and why this specialization would evolve. Here, we conducted experiments on the phylogeneticall...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392395/ https://www.ncbi.nlm.nih.gov/pubmed/30847102 http://dx.doi.org/10.1002/ece3.4912 |
_version_ | 1783398472976695296 |
---|---|
author | Valdes, Leah Laidre, Mark E. |
author_facet | Valdes, Leah Laidre, Mark E. |
author_sort | Valdes, Leah |
collection | PubMed |
description | All living organisms must eventually die, though in some cases their death can bring life‐giving opportunities. Few studies, however, have experimentally tested how animals capitalize on conspecific death and why this specialization would evolve. Here, we conducted experiments on the phylogenetically most closely‐related marine and terrestrial hermit crabs to investigate the evolution of responses to death during the sea‐to‐land transition. In the sea, death of both conspecifics and heterospecifics generates unremodeled shells needed by marine hermit crabs. In contrast, on land, terrestrial hermit crabs are specialized to live in architecturally remodeled shells, and the sole opportunity to acquire these essential resources is conspecific death. We experimentally tested these different species’ responsiveness to the scent of conspecific versus heterospecific death, predicting that conspecific death would have special attractive value for the terrestrial species. We found the terrestrial species was overwhelmingly attracted to conspecific death, rapidly approaching and forming social groupings around conspecific death sites that dwarfed those around heterospecific death sites. This differential responsiveness to conspecific versus heterospecific death was absent in marine species. Our results thus reveal that on land a reliance on resources associated exclusively with conspecifics has favored the evolution of an extreme collective attraction to conspecific death. |
format | Online Article Text |
id | pubmed-6392395 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63923952019-03-07 Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death Valdes, Leah Laidre, Mark E. Ecol Evol Original Research All living organisms must eventually die, though in some cases their death can bring life‐giving opportunities. Few studies, however, have experimentally tested how animals capitalize on conspecific death and why this specialization would evolve. Here, we conducted experiments on the phylogenetically most closely‐related marine and terrestrial hermit crabs to investigate the evolution of responses to death during the sea‐to‐land transition. In the sea, death of both conspecifics and heterospecifics generates unremodeled shells needed by marine hermit crabs. In contrast, on land, terrestrial hermit crabs are specialized to live in architecturally remodeled shells, and the sole opportunity to acquire these essential resources is conspecific death. We experimentally tested these different species’ responsiveness to the scent of conspecific versus heterospecific death, predicting that conspecific death would have special attractive value for the terrestrial species. We found the terrestrial species was overwhelmingly attracted to conspecific death, rapidly approaching and forming social groupings around conspecific death sites that dwarfed those around heterospecific death sites. This differential responsiveness to conspecific versus heterospecific death was absent in marine species. Our results thus reveal that on land a reliance on resources associated exclusively with conspecifics has favored the evolution of an extreme collective attraction to conspecific death. John Wiley and Sons Inc. 2019-02-10 /pmc/articles/PMC6392395/ /pubmed/30847102 http://dx.doi.org/10.1002/ece3.4912 Text en © 2019 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Valdes, Leah Laidre, Mark E. Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death |
title | Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death |
title_full | Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death |
title_fullStr | Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death |
title_full_unstemmed | Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death |
title_short | Scent of death: Evolution from sea to land of an extreme collective attraction to conspecific death |
title_sort | scent of death: evolution from sea to land of an extreme collective attraction to conspecific death |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6392395/ https://www.ncbi.nlm.nih.gov/pubmed/30847102 http://dx.doi.org/10.1002/ece3.4912 |
work_keys_str_mv | AT valdesleah scentofdeathevolutionfromseatolandofanextremecollectiveattractiontoconspecificdeath AT laidremarke scentofdeathevolutionfromseatolandofanextremecollectiveattractiontoconspecificdeath |