AimThe aim was to characterize the temporal dynamics of the Sahul-Sunda floristic exchange using published dated molecular phylogenies.Location The Sahul and Sunda shelves in Australasia and Southeast Asia.Methods Dated molecular phylogenies were compiled from the literature for plant clades that contained at least one node representing a biogeographical disjunction between the Sahul and Sunda shelves. For these nodes the age, ancestral geographical area and propagule type were determined.Results We analysed 49 clades from 21 published phylogenies representing a diverse set of angiosperm lineages. The inferred age of the disjunctions ranged from c. 33 Ma to c. 1 Ma; the earliest age marked the onset of the SahulSunda floristic exchange. Disjunctions (resulting from dispersal/migration events) occurred at the rate of 0.41 per 2 Myr between 34 and 12 Ma. Thereafter the rate sharply increased, coincident with the shelves effectively merging. For nearly two-thirds (63%) of the nodes Sunda was the ancestral area, and for 90% the ancestral species possessed zoochorous propagules.Main conclusions There is strong support for a dynamic model of floristic exchange between Sahul and Sunda. Fewer (18%) disjunctions occurred prior to Sahul and Sunda merging around 12 Ma, which we attribute to a combination of the effect of overwater dispersal barriers and relatively stable, saturated species assemblages resistant to the establishment of newly arrived lineages. The exchange, once underway, was strongly asymmetrical; eastwards migration into Sahul predominated over the reverse by a factor of c. 2.4. As zoochorous lineages were overrepresented among the successful dispersers, we infer a strong role for localized animal dispersal across narrow water barriers.
Aim Biodiversity studies typically use species, or more recently phylogenetic diversity (PD), as their analysis unit and produce a single map of observed diversity. However, observed biodiversity is not necessarily an indicator of significant biodiversity and therefore should not be used alone. By applying a small number of additional metrics to PD, with associated statistical tests, we can determine whether more or less of the phylogeny occurs in an area, whether branch lengths in an area are longer or shorter, and whether more long or short-branched endemism occurs in an area, than expected under a null model. Location Australian continent.Methods We used a phylogeny sampling 90% of Australia's angiosperm genera, and 3.4 million georeferenced plant specimens downloaded from Australia's Virtual Herbarium (AVH), to calculate PD, relative phylogenetic diversity (RPD) and relative phylogenetic endemism (RPE). Categorical analysis of neo-and palaeo-endemism (CANAPE) and randomization tests were performed to determine statistical significance.Results We identify several combinations of significant PD and endemism across the continent that are not seen using observed diversity patterns alone. Joint interpretation of these combinations complements the previous interpretations of Australia's plant evolutionary history. Of conservation concern, only 42% of the significant endemism cells found here overlap with existing nature reserves.Main conclusions These spatial phylogenetic methods are feasible to apply to a whole flora at the continental scale. Observed richness or PD is inadequate to fully understand the patterns of biodiversity. The combination of statistical tests applied here can be used to better explain biodiversity patterns and the evolutionary and ecological processes that have created them. The spatial phylogenetic methods used in this paper can be also be used to identify conservation priorities at any geographical scale or taxonomic level.
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