Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation

<p>Abstract</p> <p>Background</p> <p>The New Zealand (NZ) cicada fauna contains two co-distributed lineages that independently colonized the isolated continental fragment in the Miocene. One extensively studied lineage includes 90% of the extant species (<it>Kikih...

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Main Authors: Marshall David C, Hill Kathy B R, Marske Katharine A, Chambers Colleen, Buckley Thomas R, Simon Chris
Format: Article
Language:English
Published: BMC 2012-09-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/12/177
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spelling doaj-54632f4c5fc347b8aeab2502002979ee2021-09-02T09:39:11ZengBMCBMC Evolutionary Biology1471-21482012-09-0112117710.1186/1471-2148-12-177Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiationMarshall David CHill Kathy B RMarske Katharine AChambers ColleenBuckley Thomas RSimon Chris<p>Abstract</p> <p>Background</p> <p>The New Zealand (NZ) cicada fauna contains two co-distributed lineages that independently colonized the isolated continental fragment in the Miocene. One extensively studied lineage includes 90% of the extant species (<it>Kikihia</it> + <it>Maoricicada</it> + <it>Rhodopsalta</it>; ca 51 spp.), while the other contains just four extant species (<it>Amphipsalta</it> – 3 spp. + <it>Notopsalta</it> – 1 sp.) and has been little studied. We examined mitochondrial and nuclear-gene phylogenies and phylogeography, Bayesian relaxed-clock divergence timing (incorporating literature-based uncertainty of molecular clock estimates) and ecological niche models of the species from the smaller radiation.</p> <p>Results</p> <p>Mitochondrial and nuclear-gene trees supported the monophyly of <it>Amphipsalta</it>. Most interspecific diversification within <it>Amphipsalta</it>-<it>Notopsalta</it> occurred from the mid-Miocene to the Pliocene. However, interspecific divergence time estimates had large confidence intervals and were highly dependent on the assumed tree prior, and comparisons of uncorrected and patristic distances suggested difficulty in estimation of branch lengths. In contrast, intraspecific divergence times varied little across analyses, and all appear to have occurred during the Pleistocene. Two large-bodied forest taxa (<it>A. cingulata, A. zelandica</it>) showed minimal phylogeographic structure, with intraspecific diversification dating to ca. 0.16 and 0.37 Ma, respectively. Mid-Pleistocene-age phylogeographic structure was found within two smaller-bodied species (<it>A. strepitans</it> – 1.16 Ma, <it>N. sericea</it> – 1.36 Ma] inhabiting dry open habitats. Branches separating independently evolving species were long compared to intraspecific branches. Ecological niche models hindcast to the Last Glacial Maximum (LGM) matched expectations from the genetic datasets for <it>A. zelandica</it> and <it>A. strepitans</it>, suggesting that the range of <it>A. zelandica</it> was greatly reduced while <it>A. strepitans</it> refugia were more extensive. However, no LGM habitat could be reconstructed for <it>A. cingulata</it> and <it>N. sericea</it>, suggesting survival in microhabitats not detectable with our downscaled climate data.</p> <p>Conclusions</p> <p>Unlike the large and continuous diversification exhibited by the <it>Kikihia-Maoricicada-Rhodopsalta</it> clade, the contemporaneous <it>Amphipsalta-Notopsalta</it> lineage contains four comparatively old (early branching) species that show only recent diversification. This indicates either a long period of stasis with no speciation, or one or more bouts of extinction that have pruned the radiation. Within <it>Amphipsalta-Notopsalta</it>, greater population structure is found in dry-open-habitat species versus forest specialists. We attribute this difference to the fact that NZ lowland forests were repeatedly reduced in extent during glacial periods, while steep, open habitats likely became more available during late Pleistocene uplift.</p> http://www.biomedcentral.com/1471-2148/12/177
collection DOAJ
language English
format Article
sources DOAJ
author Marshall David C
Hill Kathy B R
Marske Katharine A
Chambers Colleen
Buckley Thomas R
Simon Chris
spellingShingle Marshall David C
Hill Kathy B R
Marske Katharine A
Chambers Colleen
Buckley Thomas R
Simon Chris
Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation
BMC Evolutionary Biology
author_facet Marshall David C
Hill Kathy B R
Marske Katharine A
Chambers Colleen
Buckley Thomas R
Simon Chris
author_sort Marshall David C
title Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation
title_short Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation
title_full Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation
title_fullStr Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation
title_full_unstemmed Limited, episodic diversification and contrasting phylogeography in a New Zealand cicada radiation
title_sort limited, episodic diversification and contrasting phylogeography in a new zealand cicada radiation
publisher BMC
series BMC Evolutionary Biology
issn 1471-2148
publishDate 2012-09-01
description <p>Abstract</p> <p>Background</p> <p>The New Zealand (NZ) cicada fauna contains two co-distributed lineages that independently colonized the isolated continental fragment in the Miocene. One extensively studied lineage includes 90% of the extant species (<it>Kikihia</it> + <it>Maoricicada</it> + <it>Rhodopsalta</it>; ca 51 spp.), while the other contains just four extant species (<it>Amphipsalta</it> – 3 spp. + <it>Notopsalta</it> – 1 sp.) and has been little studied. We examined mitochondrial and nuclear-gene phylogenies and phylogeography, Bayesian relaxed-clock divergence timing (incorporating literature-based uncertainty of molecular clock estimates) and ecological niche models of the species from the smaller radiation.</p> <p>Results</p> <p>Mitochondrial and nuclear-gene trees supported the monophyly of <it>Amphipsalta</it>. Most interspecific diversification within <it>Amphipsalta</it>-<it>Notopsalta</it> occurred from the mid-Miocene to the Pliocene. However, interspecific divergence time estimates had large confidence intervals and were highly dependent on the assumed tree prior, and comparisons of uncorrected and patristic distances suggested difficulty in estimation of branch lengths. In contrast, intraspecific divergence times varied little across analyses, and all appear to have occurred during the Pleistocene. Two large-bodied forest taxa (<it>A. cingulata, A. zelandica</it>) showed minimal phylogeographic structure, with intraspecific diversification dating to ca. 0.16 and 0.37 Ma, respectively. Mid-Pleistocene-age phylogeographic structure was found within two smaller-bodied species (<it>A. strepitans</it> – 1.16 Ma, <it>N. sericea</it> – 1.36 Ma] inhabiting dry open habitats. Branches separating independently evolving species were long compared to intraspecific branches. Ecological niche models hindcast to the Last Glacial Maximum (LGM) matched expectations from the genetic datasets for <it>A. zelandica</it> and <it>A. strepitans</it>, suggesting that the range of <it>A. zelandica</it> was greatly reduced while <it>A. strepitans</it> refugia were more extensive. However, no LGM habitat could be reconstructed for <it>A. cingulata</it> and <it>N. sericea</it>, suggesting survival in microhabitats not detectable with our downscaled climate data.</p> <p>Conclusions</p> <p>Unlike the large and continuous diversification exhibited by the <it>Kikihia-Maoricicada-Rhodopsalta</it> clade, the contemporaneous <it>Amphipsalta-Notopsalta</it> lineage contains four comparatively old (early branching) species that show only recent diversification. This indicates either a long period of stasis with no speciation, or one or more bouts of extinction that have pruned the radiation. Within <it>Amphipsalta-Notopsalta</it>, greater population structure is found in dry-open-habitat species versus forest specialists. We attribute this difference to the fact that NZ lowland forests were repeatedly reduced in extent during glacial periods, while steep, open habitats likely became more available during late Pleistocene uplift.</p>
url http://www.biomedcentral.com/1471-2148/12/177
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