Implications of using different metrics for niche analysis in ecological communities
Explaining the mechanisms driving niche partitioning among species is of great importance in ecology. Unlike the fundamental niche, a species' realised niche can only be measured in situ, as a result of biotic and abiotic interactions defining its size. Following current methodology, the realis...
| Autores: | , , , , , , |
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| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2019 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2445/151378 |
| Acceso en línea: | https://hdl.handle.net/2445/151378 |
| Access Level: | acceso abierto |
| Palabra clave: | Esculls coral·lins Ecologia marina Coral reefs and islands Marine ecology |
| Sumario: | Explaining the mechanisms driving niche partitioning among species is of great importance in ecology. Unlike the fundamental niche, a species' realised niche can only be measured in situ, as a result of biotic and abiotic interactions defining its size. Following current methodology, the realised niche of a species is often influenced by the rare and divergent individuals of the community sampled. In this study, using fish on coral and temperate reefs as an example, behavioural empirical data were collected to estimate realised niche sizes and niche overlaps. Niche measurements were made using the total area of the convex hull (TA), but as an alternative, a metric not as strongly influenced by sample size, standard ellipse area (SEA), was also used. A comprehensive description is given, and context-dependent pros and cons of using both metrics are discussed. Additionally, an alternative sample size correction was presented for both metrics. The analyses revealed large differences in the sizes of realised niches and their overlaps between species depending on the measurement metric used. Regardless of the species, niche size and overlap were always larger for TA than SEA. Increasing sample size reduced niche size variability for both TA and SEA, but the variation was always smaller for SEA than TA. We successfully adapted the SEA metric for analysis of behavioural niche components and demonstrated that measuring niche sizes using the 2 metrics, each with their own strengths and weaknesses, can produce contradictory results, the ecological consequences of which are likely to be important. |
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