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. 2020 Jan 29;287(1919):20192546.
doi: 10.1098/rspb.2019.2546. Epub 2020 Jan 22.

Extinction pulse at Eocene-Oligocene boundary drives diversification dynamics of two Australian temperate floras

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Extinction pulse at Eocene-Oligocene boundary drives diversification dynamics of two Australian temperate floras

Francis J Nge et al. Proc Biol Sci. .

Abstract

The diversification dynamics of the Australian temperate flora remains poorly understood. Here, we investigate whether differences in plant richness in the southwest Australian (SWA) biodiversity hotspot and southeast Australian (SEA) regions of the Australian continent can be attributed to higher net diversification, more time for species accumulation, or both. We assembled dated molecular phylogenies for the 21 most species-rich flowering plant families found across mesic temperate Australia, encompassing both SWA and SEA regions, and applied a series of diversification models to investigate responses across different groups and timescales. We show that the high richness in SWA can be attributed to a higher net rate of lineage diversification and more time for species accumulation. Different pulses of diversification were retrieved in each region. A decrease in diversification rate across major flowering plant lineages at the Eocene-Oligocene boundary (ca 34 Ma) was witnessed in SEA but not in SWA. Our study demonstrates the importance of historical diversification pulses and differential responses to global events as drivers of present-day diversity. More broadly, we show that diversity within the SWA biodiversity hotspot is not only the result of recent radiations, but also reflects older events over the history of this planet.

Keywords: Australian flora; biodiversity hotspots; diversification rates; extinction; macroevolution; radiation.

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Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1.
Figure 1.
Representative diversity of the Australian temperate flora (a) Eucalyptus macrocarpa Hook.; (b) Gompholobium cyaninum Chappill; (c) Hyalosperma cotula (Benth.) Paul G. Wilson; (d) Thysanotus R.Br.; (e) Banksia baueri R.Br.; (f) Stenanthemum nanum Rye; (g) Anigozanthos manglesii D. Don; (h) Drosera barbigera Plach.; (i) Gompholobium confertum (DC.) Crisp; (j) Drosera erythrorhiza subsp. squamosa (Benth.) N. G. Marchant & Lowrie; (k) Synaphea sp. Darkin (F. Hort et al. 586); (l) Thelymitra epipactoides F. Muell.; (m) map of Australia shaded by topographic contours, with southwest and southeast defined by their respective IBRA regions (see methods in the electronic supplementary materials). Photographs: F. J. Nge. (Online version in colour.)
Figure 2.
Figure 2.
Lineage-diversification-through-time plots, with number of generic divergences across 10 Myr (from 70 to 40 Myr) and 5 Myr (from 40 to 0 Myr) time-bins for the SWA and SEA temperate regions. Points are actual values across each time-bin (green diamonds, southwest; orange squares, southeast). The trend lines show the moving average across each time-bin (green dotted, southwest; orange smooth, southeast). (a) Total genera; (b) monotypic genera; (c) Proteaceae; (d) Mirbelieae, Fabaceae; (e) Ericaceae; (f) Chamelaucieae, Myrtaceae; (g) Restionaceae; (h) Cyperaceae; (i) Rutaceae; (j) Asteraceae. Grey horizontal trend lines track the change in mean sea surface temperature, adapted from [42]. (a–i) Vertical grey lines mark the Eocene–Oligocene boundary; (j) the vertical grey bar marks the Mid-Miocene Climatic Optimum. Illustrations were sourced from www.plantillustrations.org and modified under the Creative Commons Attribution 2.0 license: (b) Cephalotus follicularis, (c) Banksia coccinea, (d) Gompholobium, (e) Styphelia triflora, (f) Darwinia macrostegia, (g) Restionaceae, (h) Schoenus nigricans, (i) Boronia heterophylla and (j) Rhodanthe manglesii. (Online version in colour.)
Figure 3.
Figure 3.
Diversification rate distributions of genera for the SWA and SEA temperate regions under the high extinction model (κ = 0.9). Net diversification rates are net speciation events per Myr per lineage (sp sp−1 My−1).

References

    1. Myers N, Mittermeier RA, Mittermeier CG, Da Fonseca GA, Kent J. 2000. Biodiversity hotspots for conservation priorities. Nature 403, 853–858. ( 10.1038/35002501) - DOI - PubMed
    1. Williams KJ, Ford A, Rosauer DF, De Silva N, Mittermeier R, Bruce C, Larsen FW, Margules C. 2011. Forests of East Australia: the 35th biodiversity hotspot. In Biodiversity hotspots (eds Zachos FE, Habel JC), pp. 295–310. London, UK: Springer.
    1. Madriñán S, Cortés AJ, Richardson JE. 2013. Páramo is the world's fastest evolving and coolest biodiversity hotspot. Front. Genet. 4, 1–7. ( 10.3389/fgene.2013.00192) - DOI - PMC - PubMed
    1. Lagomarsino LP, Condamine FL, Antonelli A, Mulch A, Davis CC. 2016. The abiotic and biotic drivers of rapid diversification in Andean bellflowers (Campanulaceae). New Phytologist 210, 1430–1442. ( 10.1111/nph.13920) - DOI - PMC - PubMed
    1. Nürk NM, Scheriau C, Madriñán S. 2013. Explosive radiation in high Andean Hypericum—rates of diversification among New World lineages. Front. in Genet. 4, 1–14. ( 10.3389/fgene.2013.00175) - DOI - PMC - PubMed

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