Determining the relative roles of species replacement and species richness differences in generating beta-diversity patterns

• Published in: Global ecology and biogeography Vol. 21; no. 7; pp. 760 - 771
• Main Authors: Carvalho, José C., Cardoso, Pedro, Gomes, Pedro
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.07.2012; Blackwell Publishing; Blackwell; Wiley Subscription Services, Inc
• Subjects: Animal and plant ecology; Animal ecology; Animal, plant and microbial ecology; Biogeography; Biological and medical sciences; Coastal ecology; Conservation biology; Diversity partitioning; Dunes; Fundamental and applied biological sciences. Psychology; General aspects; interspecific variation; MACROECOLOGICAL METHODS; Mathematical constants; methodology; Multiculturalism & pluralism; nestedness; richness gradient; similarity indices; Species; Species diversity; species loss; species replacement; Spiders; Synecology; similarity indices; Loss; species replacement; Biogeography; species loss; Beta diversity; Ecology; Replacement; Diversity partitioning; richness gradient; Similarity indice; Nested subset; nestedness; Species richness
• ISSN: 1466-822X; 1466-8238; 1466-822X
• DOI: 10.1111/j.1466-8238.2011.00694.x

Aim: To determine the relative contribution of species replacement and species richness differences to the emergence of beta-diversity patterns. Innovation: A novel method that disentangles all compositional differences (β cc , overall beta diversity) in its two components, species replacement (β -3 ) and species richness differences (β rich ) is proposed. The performance of the method was studied with ternary plots, which allow visualization of the influence of the relative proportions of shared and unique species of two sites over each metric. The method was also tested in different hypothetical gradients and with real datasets. The novel method was compared with a previous proposal based on the partitioning of overall compositional differences (β sor ) in replacement (β sim ) and nestedness (β nes ). The linear response of β cc contrasts with the curvilinear response of β sor to linear gradients of dissimilarity. When two sites did not share any species, β sim was always 1 and β -3 only reached 1 when the number of exclusive species of both sites was equal. β -3 remained constant along gradients of richness differences with constant replacement, while β sim decreased. β rich had a linear response to a linear gradient of richness differences with constant species replacement, whereas β nes exhibited a hump-shaped response. Moreover, β sim > β nes when clearly almost all species of one site were lost, whereas β -3 < β rich in the same circumstances. Main conclusions: The behaviour of the partition of β cc into β -3 and β rich is consistent with the variation of replacement and richness differences. The partitioning of β sor into β sim and β nes overestimates the replacement component and underestimates richness differences. The novel methodology allows the discrimination of different causes of beta-diversity patterns along latitudinal, biogeographic or ecological gradients, by estimating correctly the relative contributions of replacement and richness differences.