Contemporary genetic structure of an endemic freshwater turtle reflects Miocene orogenesis of New Guinea

被引:37
|
作者
Georges, Arthur [1 ]
Zhang, Xiuwen [1 ]
Unmack, Peter [1 ]
Reid, Brenden N. [2 ]
Minh Le [3 ,4 ,5 ]
McCord, William P. [6 ]
机构
[1] Univ Canberra, Inst Appl Ecol, Canberra, ACT 2601, Australia
[2] Univ Wisconsin, Dept Forest & Wildlife Ecol, Madison, WI 53706 USA
[3] Hanoi Univ Sci, Fac Environm Sci, Hanoi, Vietnam
[4] Ctr Nat Resources & Environm Studies, Hanoi, Vietnam
[5] Amer Museum Nat Hist, Dept Herpetol, New York, NY 10024 USA
[6] East Fishkill Anim Hosp, Hopewell Jct, NY 12533 USA
关键词
Birds Head; Chelidae; Elseya novaeguineae; Indonesia; Langguru Fold Belt; molecular clock; Papua; tectonics; Vogelkop; DOWNS LOCAL FAUNA; PAPUA-NEW-GUINEA; SEA-LEVEL CHANGE; MITOCHONDRIAL-DNA; PHYLOGENETIC-RELATIONSHIPS; CLIMATIC EVENTS; CONTROL REGION; AUSTRALIA; PHYLOGEOGRAPHY; BIOGEOGRAPHY;
D O I
10.1111/bij.12176
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The island of New Guinea lies in one of the most tectonically active regions in the world and has long provided outstanding opportunity for studies of biogeography. Several chelid turtles, of clear Gondwanal origin, occur in New Guinea; all species except one, the endemic Elseya novaeguineae, are restricted to the lowlands south of the Central Ranges. Elseya novaeguineae is found throughout New Guinea. We use mitochondrial and nuclear gene variation among populations of E.novaeguineae throughout its range to test hypotheses of recent extensive dispersal versus more ancient persistence in New Guinea. Its genetic structure bears the signature of Miocene vicariance events. The date of the divergence between a Birds Head (Kepala Burung) clade and clades north and south of the Central Ranges is estimated to be 19.8Mya [95% highest posterior density (HPD) interval of 13.3-26.8Mya] and the date between the northern and southern clades is estimated to be slightly more recent at 17.4Mya (95% HPD interval of 11.0-24.5Mya). The distribution of this endemic species is best explained by persistent occupation (or early invasion and dispersal) and subsequent isolation initiated by the dramatic landform changes that were part of the Miocene history of the island of New Guinea, rather than as a response to the contemporary landscape of an exceptionally effective disperser. The driving influence on genetic structure appears to have been isolation arising from a combination of: (1) the early uplift of the Central Ranges and establishment of a north-south drainage divide; (2) development of the Langguru Fold Belt; (3) the opening of Cenderawasih Bay; and (4) the deep waters of the Aru Trough and Cenderawasih Bay that come close to the current coastline to maintain isolation of the Birds Head through periods of sea level minima (-135m). The dates of divergence of turtle populations north and south of the ranges predate the telescopic uplift of the central ranges associated with oblique subduction of the Australian Plate beneath the Pacific Plate. Their isolation was probably associated with earlier uplift and drainage isolation driven by the accretion of island terranes to the northern boundary of the Australian craton that occurred earlier than the oblique subduction. The opening of Cenderawasih Bay is too recent (6 Mya) to have initiated the isolation of the Birds Head populations from those of the remainder of New Guinea, although its deep waters will have served to sustain the isolation through successive sea level changes. The molecular evidence suggests that the Birds Head docked with New Guinea some time before the Central Ranges emerged as a barrier to turtle dispersal. Overall, deep genetic structure of the species complex reflects events and processes that occurred during Miocene, whereas structure within each clade across the New Guinea landscape relates to Pliocene and Pleistocene times.(c) 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2014, 111, 192-208.
引用
收藏
页码:192 / 208
页数:17
相关论文
共 50 条
  • [31] Population genetic structure of New Zealand's endemic corophiid amphipods: evidence for allopatric speciation
    Stevens, MI
    Hogg, ID
    BIOLOGICAL JOURNAL OF THE LINNEAN SOCIETY, 2004, 81 (01) : 119 - 133
  • [32] Population genetic structure of the endemic rosewoods Dalbergia cochinchinensis and D. oliveri at a regional scale reflects the Indochinese landscape and life-history traits
    Hartvig, Ida
    So, Thea
    Changtragoon, Suchitra
    Hoa Thi Tran
    Bouamanivong, Somsanith
    Theilade, Ida
    Kjaer, Erik Dahl
    Nielsen, Lene Rostgaard
    ECOLOGY AND EVOLUTION, 2018, 8 (01): : 530 - 545
  • [33] Population genetic structure in the endemic cyprinid fish Microphysogobio alticorpus in Taiwan: Evidence for a new phylogeographical area
    Jean, Chuen-Tan
    Wu, Chien-Yu
    Tsai, Kun-Chan
    Wang, Wei-Kuang
    Hsu, Yuan-Yuan
    Chang, Yuan-Mou
    Lin, Hung-Du
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2014, 57 : 108 - 116
  • [34] Genetic structure of Mycosphaerella fijiensis populations from Australia, Papua New Guinea and the Pacific Islands
    Hayden, HL
    Carlier, J
    Aitken, EAB
    PLANT PATHOLOGY, 2003, 52 (06) : 703 - 712
  • [35] Phylogeny and population genetic structure of the ant genus Acropyga (Hymenoptera : Formicidae) in Papua New Guinea
    Janda, Milan
    Matos-Maravi, Pavel
    Borovanska, Michaela
    Zima, Jan, Jr.
    Youngerman, Eric
    Pierce, Naomi E.
    INVERTEBRATE SYSTEMATICS, 2016, 30 (01) : 28 - 40
  • [36] Genetic Mechanism of Inversion Anticline Structure at the End of Miocene in Xihu Sag, East China Sea: A New Understanding of Basement Structure Difference
    Jiang Y.
    Zou W.
    Liu J.
    Tang X.
    He X.
    Diqiu Kexue - Zhongguo Dizhi Daxue Xuebao/Earth Science - Journal of China University of Geosciences, 2020, 45 (03): : 968 - 979
  • [37] Assessment of the Genetic Diversity and Structure of the Korean Endemic Freshwater Fish Microphysogobio longidorsalis (Gobioninae) Using Microsatellite Markers: A First Glance from Population Genetics
    Kim, Kang-Rae
    Sung, Mu-Sung
    Hwang, Yujin
    Jeong, Ju Hui
    Yu, Jeong-Nam
    GENES, 2024, 15 (01)
  • [38] Small spatial scale population genetic structure in two limpet species endemic to the Kermadec Islands, New Zealand
    Wood, Ann R.
    Gardner, Jonathan P. A.
    MARINE ECOLOGY PROGRESS SERIES, 2007, 349 : 159 - 170
  • [39] Population structure and dispersal of the freshwater mosquitoes Culex annulirostris and Culex palpalis (Diptera: Culicidae) in Papua New Guinea and northern Australia
    Chapman, HF
    Hughes, JM
    Ritchie, SA
    Kay, BH
    JOURNAL OF MEDICAL ENTOMOLOGY, 2003, 40 (02) : 165 - 169
  • [40] The population genetic structure of a common tropical damselfish on the Great Barrier Reef and eastern Papua New Guinea
    D. B. Jones
    D. R. Jerry
    M. I. McCormick
    L. K. Bay
    Coral Reefs, 2010, 29 : 455 - 467