Endangered Rough Pigtoe Pearlymussel: Assessment of Phylogenetic Status and Genetic Differentiation of Two Disjunct Populations

被引:5
|
作者
Jones, Jess W. [1 ]
Johnson, Nathan [2 ]
Grobler, Paul [3 ]
Schilling, Daniel [2 ]
Neves, Richard J. [2 ]
Hallerman, Eric M. [2 ]
机构
[1] Virginia Polytech Inst & State Univ, US Fish & Wildlife Serv, Dept Fish & Wildlife Conservat, Blacksburg, VA 24061 USA
[2] Virginia Polytech Inst & State Univ, Dept Fish & Wildlife Conservat, Blacksburg, VA 24061 USA
[3] Univ Orange Free State, Dept Genet, ZA-9300 Bloemfontein, South Africa
来源
基金
美国食品与农业研究所;
关键词
Rough pigtoe; Pleurobema plenum; endangered species; freshwater mussel; mitochondrial DNA; nuclear DNA microsatellites; FRESH-WATER MUSSELS; INTEGRATED SOFTWARE; UNIONIDAE; BIVALVIA; CONSERVATION;
D O I
10.3996/052013-JFWM-036
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
We conducted a genetic characterization of two extant populations of an endangered freshwater mussel, the rough pigtoe Pleurobema plenum, in the Clinch River, Tennessee of the Tennessee River basin, and the Green River, Kentucky, of the Ohio River basin for purposes of conservation recovery planning. First, phylogenetic status of this species within the Pleurobema cordatum species complex (P. cordatum, plenum, rubrum, sintoxia) was assessed using mitochondrial ND1 deoxyribonucleic acid (DNA) sequences, which showed that all investigated species of Pleurobema are genetically distinct. Our results indicated that P. cordatum, P. plenum, P. rubrum, and P. sintoxia each represent monophyletic clades; however, the latter two species were closely related, separated by only one to three nucleotide differences. Further, DNA sequence haplotypes from both populations of P. plenum grouped together into one monophyletic clade and did not support characterizing the populations as separate species. Thus, our phylogenetic analysis confirms that populations of P. plenum in the Clinch and Green rivers are the same species. Second, we assessed genetic differentiation between P. plenum populations in each river by analyzing variation at eight nuclear DNA microsatellite loci, where F-ST (= 0.023) and Jost's D (= 0.175) indicated genetically differentiated populations. Because these populations are geographically and demographically independent, and differentiated at nuclear microsatellite loci, recognition as management units is recommended. Additional studies are needed to determine whether there are differences at adaptiveor life-history traits, such as fish host usage, shell morphology, and soft anatomy between populations, and to further investigate the phylogenetic relationship of P. rubrum and P. sintoxia.
引用
收藏
页码:338 / 349
页数:12
相关论文
共 50 条
  • [31] Low genetic diversity and high genetic differentiation among severely fragmented populations of the critically endangered tree Talbotiella gentii (Fabaceae)
    Dompreh, D.
    Swaine, M. D.
    Price, A.
    SOUTHERN FORESTS-A JOURNAL OF FOREST SCIENCE, 2011, 73 (02) : 73 - 80
  • [32] Genetic differences between the two remaining wild populations of the endangered Indian rhinoceros (Rhinoceros unicomis)
    Zschokke, Samuel
    Armbruster, Georg F. J.
    Ursenbacher, Sylvain
    Baur, Bruno
    BIOLOGICAL CONSERVATION, 2011, 144 (11) : 2702 - 2709
  • [33] Assessment of genetic and morphological differentiation among populations of the Diederik Cuckoo Chrysococcyx caprius
    Smith, Rae M.
    Dalton, Desire L.
    Mwale, Monica
    Nupen, Lisa J.
    Pretorius, Chantelle
    Bojko, Jamie
    Labuschagne, Kim
    Russo, Isa-Rita M.
    Osinubi, Samuel T.
    OSTRICH, 2023, 94 (02) : 86 - 99
  • [34] Rapid genetic differentiation between ex situ and their in situ source populations: an example of the endangered Silene otites (Caryophyllaceae)
    Lauterbach, Daniel
    Burkart, Michael
    Gemeinholzer, Birgit
    BOTANICAL JOURNAL OF THE LINNEAN SOCIETY, 2012, 168 (01) : 64 - 75
  • [35] Low genetic differentiation in north-west European populations of the locally endangered root vole, Microtus oeconomus
    Leijs, R
    van Apeldoorn, RC
    Bijlsma, R
    BIOLOGICAL CONSERVATION, 1999, 87 (01) : 39 - 48
  • [36] High genetic differentiation among remnant populations of the endangered Caesalpinia echinata Lam. (Leguminosae-Caesalpinioideae)
    Cardoso, MA
    Provan, J
    Powell, W
    Ferreira, PCG
    De Oliveira, DE
    MOLECULAR ECOLOGY, 1998, 7 (05) : 601 - 608
  • [37] Genetic differentiation within and among island populations of the endangered plant Aster miyagii (Asteraceae), an endemic to the Ryukyu Islands
    Maki, M
    AMERICAN JOURNAL OF BOTANY, 2001, 88 (12) : 2189 - 2194
  • [38] High genetic diversity and extreme differentiation in the two remaining populations of Habromys simulatus
    Castaneda-Rico, Susette
    Leon-Paniagua, Livia
    Ruedas, Luis A.
    Vazquez-Dominguez, Ella
    JOURNAL OF MAMMALOGY, 2011, 92 (05) : 963 - 973
  • [39] Assessment of genetic diversity and phylogenetic relationships of endangered endemic plant Barbarea integrifolia DC. (Brassicaceae) in Turkey
    Filiz, Ertugrul
    Osma, Etem
    Kandemir, Ali
    Tombuloglu, Huseyin
    Tombuloglu, Guzin
    Birbilener, Seda
    Aydin, Mehtap
    TURKISH JOURNAL OF BOTANY, 2014, 38 (06) : 1169 - 1181
  • [40] High genetic divergence and low genetic variability in disjunct populations of the endemic Vellozia compacta (Velloziaceae) occurring in two edaphic environments of Brazilian campos rupestres
    Júnia Maria Lousada
    Maria Bernadete Lovato
    Eduardo Leite Borba
    Brazilian Journal of Botany, 2013, 36 : 45 - 53