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BIODIVERSITY RESEARCH: Conserving macroinvertebrate diversity in headwater streams: the importance of knowing the relative contributions of α and β diversity
Author(s) -
Clarke Amber,
Mac Nally Ralph,
Bond Nick R.,
Lake P. S.
Publication year - 2010
Publication title -
diversity and distributions
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.918
H-Index - 118
eISSN - 1472-4642
pISSN - 1366-9516
DOI - 10.1111/j.1472-4642.2010.00692.x
Subject(s) - biological dispersal , ecology , biodiversity , diversity (politics) , species richness , streams , gamma diversity , species diversity , ecosystem diversity , invertebrate , beta diversity , geography , environmental science , biology , population , computer science , computer network , demography , sociology , anthropology
Aim  We investigated partitioning of aquatic macroinvertebrate diversity in eight headwater streams to determine the relative contributions of α and β diversity to γ diversity, and the scale dependence of α and β components. Location  Great Dividing Range, Victoria, Australia. Methods  We used the method of Jost ( Ecology , 2007, 88, 2427–2439) to partition γ diversity into its α and β components. We undertook the analyses at both reach and catchment scales to explore whether inferences depended on scale of observation. Results  We hypothesized that β diversity would make a large contribution to the γ diversity of macroinvertebrates in our dendritic riverine landscape, particularly at the larger spatial scale (among catchments) because of limited dispersal among sites and especially among catchments. However, reaches each had relatively high taxon richness and high α diversity, while β diversity made only a small contribution to γ diversity at both the reach and catchment scales. Main conclusions  Dendritic riverine landscapes have been thought to generate high β diversity as a consequence of limited dispersal and high heterogeneity among individual streams, but this may not hold for all headwater stream systems. Here, α diversity was high and β diversity low, with individual headwater stream reaches each containing a large portion of γ diversity. Thus, each stream could be considered to have low irreplaceability since losing the option to use one of these sites in a representative reserve network does not greatly diminish the options available for completing the reserve network. Where limited information on individual taxonomic distributions is available, or time and money for modelling approaches are limited, diversity partitioning may provide a useful ‘first‐cut’ for obtaining information about the irreplaceability of individual streams or subcatchments when establishing representative freshwater reserves.

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