The study of diversity has become increasingly sophisticated, including the use of measures of phylogenetic diversity. We calculate the spatial variation in species richness, taxonomic beta diversity, and alpha and beta phylogenetic diversity ( We compare the congruence of phylogenetic and taxonomic diversity patterns, and also compare Species richness and Communities in the southern and south‐eastern regions were dominated by species from the large family Gonyleptidae, presenting a high richness and a low Phylogenetic diversity may be of special importance to assess the conservation value of distantly related lineages. These species‐poor groups are less likely to influence taxonomic‐based diversity analyses, but their importance for conservation arises from their phylogenetic distinctiveness, captured by
Assessments of spatial patterns of biodiversity change are essential to detect a signature of anthropogenic impacts, inform monitoring and conservation programs, and evaluate implications of biodiversity loss to humans. While taxonomic diversity (
- PAR ID:
- 10045576
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Global Change Biology
- Volume:
- 23
- Issue:
- 8
- ISSN:
- 1354-1013
- Page Range / eLocation ID:
- p. 2999-3011
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract PD α andPD β , respectively) of Atlantic Forest harvestman communities using a data set containing 556 species from 68 sites, distributed in 12 Brazilian states.PD α with null model expectations, to check for phylogenetic clustering or overdispersion in communities.PD α are correlated, peaking in southern and south‐eastern coastal sites and decreasing towards the interior and towards the north‐east.PD α in north‐eastern sites was higher than expected, while a clustered phylogenetic pattern characterised most other sites.PD α . As the dominance of Gonyleptidae decreased towards the north, where local communities have fewer species, but a higherPD α , they contain representatives of other families. The beta diversity was more sensitive to the compositional changes involving closely related Gonyleptidae species, whilePD β is more influenced by deeper phylogenetic compositional changes, between more distant lineages.PD α andPD β measures. -
Abstract Estimates of recent biodiversity change remain inconsistent, debated, and infrequently assessed for their functional implications. Here, we report that spatial scale and type of biodiversity measurement influence evidence of temporal biodiversity change. We show a pervasive scale dependence of temporal trends in taxonomic (TD) and functional (FD) diversity for an ~50-year record of avian assemblages from North American Breeding Bird Survey and a record of global extinctions. Average TD and FD increased at all but the global scale. Change in TD exceeded change in FD toward large scales, signaling functional resilience. Assemblage temporal dissimilarity and turnover (replacement of species or functions) declined, while nestedness (tendency of assemblages to be subsets of one another) increased with scale. Patterns of FD change varied strongly among diet and foraging guilds. We suggest that monitoring, policy, and conservation require a scale-explicit framework to account for the pervasive effect that scale has on perceived biodiversity change.
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Abstract Aims Bryophytes can cover three quarters of the ground surface, play key ecological functions, and increase biodiversity in mesic high‐elevation conifer forests of the temperate zone. Forest gaps affect species coexistence (and ecosystem functions) as suggested by the gap and gap‐size partitioning hypotheses (
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USA .Methods We characterized canopy openness, microclimate, forest floor substrates, vascular vegetation cover, and moss layer (cover, common species, and functional attributes) in three canopy openness environments (gap, gap edge, forest canopy) across 20 gaps (fir waves) (
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