Climate, physiological tolerance and sex-biased dispersal shape genetic structure of Neotropical orchid bees

被引:61
|
作者
Lopez-Uribe, Margarita M. [1 ]
Zamudio, Kelly R. [2 ]
Cardoso, Carolina F. [3 ]
Danforth, Bryan N. [1 ]
机构
[1] Cornell Univ, Dept Entomol, Ithaca, NY 14853 USA
[2] Cornell Univ, Dept Ecol & Evolutionary Biol, Ithaca, NY 14853 USA
[3] Univ Fed Minas Gerais, Lab Sistemat & Ecol Abelhas, BR-30123970 Belo Horizonte, MG, Brazil
基金
美国国家科学基金会;
关键词
Palaeomodeling; anonymous single copy nuclear loci; mitochondrial DNA; euglossine bees; nuclear DNA; Pleistocene refugia; COMPARATIVE PHYLOGEOGRAPHY; SPECIES DISTRIBUTIONS; EUGLOSSINE BEES; PATTERNS; BIODIVERSITY; HYMENOPTERA; DISTANCE; NUCLEAR; MODELS; CONSERVATION;
D O I
10.1111/mec.12689
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Understanding the impact of past climatic events on the demographic history of extant species is critical for predicting species' responses to future climate change. Palaeoclimatic instability is a major mechanism of lineage diversification in taxa with low dispersal and small geographical ranges in tropical ecosystems. However, the impact of these climatic events remains questionable for the diversification of species with high levels of gene flow and large geographical distributions. In this study, we investigate the impact of Pleistocene climate change on three Neotropical orchid bee species (Eulaema bombiformis, E.meriana and E.cingulata) with transcontinental distributions and different physiological tolerances. We first generated ecological niche models to identify species-specific climatically stable areas during Pleistocene climatic oscillations. Using a combination of mitochondrial and nuclear markers, we inferred calibrated phylogenies and estimated historical demographic parameters to reconstruct the phylogeographical history of each species. Our results indicate species with narrower physiological tolerance experienced less suitable habitat during glaciations and currently exhibit strong population structure in the mitochondrial genome. However, nuclear markers with low and high mutation rates show lack of association with geography. These results combined with lower migration rate estimates from the mitochondrial than the nuclear genome suggest male-biased dispersal. We conclude that despite large effective population sizes and capacity for long-distance dispersal, climatic instability is an important mechanism of maternal lineage diversification in orchid bees. Thus, these Neotropical pollinators are susceptible to disruption of genetic connectivity in the event of large-scale climatic changes.
引用
收藏
页码:1874 / 1890
页数:17
相关论文
共 50 条
  • [31] Population structure and sex-biased dispersal in the forest dwelling vespertilionid bat, Myotis septentrionalis
    Arnold, Bryan D.
    AMERICAN MIDLAND NATURALIST, 2007, 157 (02): : 374 - 384
  • [32] Fine-scale population genetic structure and sex-biased dispersal in the smooth snake (Coronella austriaca) in southern England
    Pernetta, A. P.
    Allen, J. A.
    Beebee, T. J. C.
    Reading, C. J.
    HEREDITY, 2011, 107 (03) : 231 - 238
  • [33] Population genetic structure and sex-biased dispersal of the hazel dormouse (Muscardinus avellanarius) in a continuous and in a fragmented landscape in central Italy
    Bani, L.
    Orioli, V.
    Pisa, G.
    Fagiani, S.
    Dondina, O.
    Fabbri, E.
    Randi, E.
    Sozio, G.
    Mortelliti, A.
    CONSERVATION GENETICS, 2017, 18 (02) : 261 - 274
  • [34] Genetic population structure of the ground beetle, Pterostichus oblongopunctatus, inhabiting a fragmented and polluted landscape: Evidence for sex-biased dispersal
    Lagisz, Malgorzata
    Wolff, Kirsten
    Sanderson, Roy A.
    Laskowski, Ryszard
    JOURNAL OF INSECT SCIENCE, 2010, 10
  • [35] Genetic evidence for sex-biased dispersal and cryptic diversity in the greater horseshoe bat, Rhinolophus ferrumequinum
    Ji Eun Jang
    Seo Yeon Byeon
    Hye Ri Kim
    Ji Young Kim
    Hyeon Ho Myeong
    Hyuk Je Lee
    Biodiversity and Conservation, 2021, 30 : 847 - 864
  • [36] Genetic evidence for sex-biased dispersal and cryptic diversity in the greater horseshoe bat, Rhinolophus ferrumequinum
    Jang, Ji Eun
    Byeon, Seo Yeon
    Kim, Hye Ri
    Kim, Ji Young
    Myeong, Hyeon Ho
    Lee, Hyuk Je
    BIODIVERSITY AND CONSERVATION, 2021, 30 (03) : 847 - 864
  • [37] Genetic Detection of Sex-Biased and Age-Biased Dispersal in a Population of Wild Carnivore, the Red Fox, Vulpes vulpes
    Gachot-Neveu, Helene
    Lefevre, Pavine
    Roeder, Jean-Jacques
    Henry, Caroline
    Poulle, Marie-Lazarine
    ZOOLOGICAL SCIENCE, 2009, 26 (02) : 145 - 152
  • [38] Fine-scale population genetic structure and short-range sex-biased dispersal in a solitary carnivore, Lutra lutra
    Quaglietta, Lorenzo
    Fonseca, Vania C.
    Hajkova, Petra
    Mira, Antonio
    Boitani, Luigi
    JOURNAL OF MAMMALOGY, 2013, 94 (03) : 561 - 571
  • [39] Social constraint and an absence of sex-biased dispersal drive fine-scale genetic structure in white-winged choughs
    Beck, N. R.
    Peakall, R.
    Heinsohn, R.
    MOLECULAR ECOLOGY, 2008, 17 (19) : 4346 - 4358
  • [40] Genetic structure and sex-biased gene flow in the history of southern African populations
    Bajic, Vladimir
    Barbieri, Chiara
    Huebner, Alexander
    Gueldemann, Tom
    Naumann, Christfried
    Gerlach, Linda
    Berthold, Falko
    Nakagawa, Hirosi
    Mpoloka, Sununguko W.
    Roewer, Lutz
    Purps, Josephine
    Stoneking, Mark
    Pakendorf, Brigitte
    AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY, 2018, 167 (03) : 656 - 671