Population genetic structure and range limits of Prostanthera cineolifera (Lamiaceae), a vulnerable shrub with a patchy distribution

被引:0
|
作者
Palsson, Ruth L. [1 ]
Telford, Ian R. H. [1 ]
Bruhl, Jeremy J. [1 ]
Andrew, Rose L. [1 ]
机构
[1] Univ New England, Sch Environm & Rural Sci, NCW Beadle Herbarium & Bot, Armidale, NSW 2351, Australia
关键词
DArTseq; Molecular analysis; Morphometric analysis; Population genetics; Prostanthera; SNP; R PACKAGE; CONSERVATION; DIVERSITY; DISPERSAL; TAXONOMY; DISTANCE; FITNESS; BIOLOGY; EDGE; FLOW;
D O I
10.1007/s10592-024-01637-3
中图分类号
X176 [生物多样性保护];
学科分类号
090705 ;
摘要
Integrating molecular data is essential for clarifying the distributions and genetic structures of species that have histories of misidentification and misapplication of names. There has been confusion about the species limits of the Vulnerable Prostanthera cineolifera with respect to morphologically similar specimens in the Hunter Valley, New South Wales, Australia and morphologically dissimilar specimens in the Lower Hawkesbury Valley, New South Wales, and from north-eastern New South Wales. To test the species limits of P. cineolifera, and related taxa, specimens were collected from across the range and augmented with herbarium specimens. We used morphometric analysis of 18 morphological characters across 51 samples. Using the DArTseq reduced representation sequencing platform, 4010 single-nucleotide polymorphisms (SNPs) across 110 individuals were recovered for molecular analysis. Both morphological and molecular analyses produced three concordant clusters (A) P. cineolifera, (B) a group sharing similarities with P. sp. Hawkesbury (B.J.Conn 2591), and (C) a group allied with P. lanceolata and P. ovalifolia. These results indicate that the specimens form north-eastern New South Wales are more likely to be P. lanceolata, not P. cineolifera, and that specimens from the Lower Hawkesbury are of an undescribed species with the phrase name P. sp. Hawkesbury (B.J.Conn 2591). Within P. cineolifera there was pronounced genetic differentiation among populations. Little evidence of inbreeding was observed, but the newly recognised, more isolated populations had the lowest genetic diversity. This study provides new information about the range of the species and its genetic structure that informs the conservation priorities for this species.
引用
收藏
页码:1231 / 1251
页数:21
相关论文
共 50 条
  • [21] Genetic population structure and range colonisation of Nezara viridula
    Pavlovcic, Petra
    Kavar, Tatjana
    Meglic, Vladimir
    Doberlet, Meta Virant
    BULLETIN OF INSECTOLOGY, 2008, 61 (01): : 191 - 192
  • [22] Genetic diversity and population structure in medicinal plant Melissa officinalis L. (Lamiaceae)
    Fahimeh Koohdar
    Masoud Sheidai
    Genetic Resources and Crop Evolution, 2022, 69 : 1753 - 1758
  • [23] Habitat distribution influences dispersal and fine-scale genetic population structure of eastern foxsnakes (Mintonius gloydi) across a fragmented landscape
    Row, Jeffrey R.
    Blouin-Demers, Gabriel
    Lougheed, Stephen C.
    MOLECULAR ECOLOGY, 2010, 19 (23) : 5157 - 5171
  • [24] Genetic Population Structure across the Range of Endangered Northeastern Bulrush, Scirpus ancistrochaetus
    Cipollini, Kendra
    Lavretsky, Philip
    Cipollini, Don
    Peters, Jeffrey L.
    INTERNATIONAL JOURNAL OF PLANT SCIENCES, 2017, 178 (01) : 67 - 78
  • [25] Genetic Population Structure and Allele Surfing During Range Expansion in Dynamic Habitats
    Braga, Rosana T.
    Rodrigues, Joao F. M.
    Diniz-Filho, Jose A. F.
    Rangel, Thiago F.
    ANAIS DA ACADEMIA BRASILEIRA DE CIENCIAS, 2019, 91 (02):
  • [26] Population genetic structure of barramundi (Lates calcarifer) across the natural distribution range in Australia informs fishery management and aquaculture practices
    Loughnan, Shannon R.
    Smith-Keune, Carolyn
    Beheregaray, Luciano B.
    Robinson, Nicholas A.
    Jerry, Dean R.
    MARINE AND FRESHWATER RESEARCH, 2019, 70 (11) : 1533 - 1542
  • [27] ISOLATION BY DISTANCE SHAPES POPULATION GENETIC STRUCTURE OF A RARE TERRESTRIAL SALAMANDER, PLETHODON PETRAEUS, WITH AN EXTREMELY SMALL RANGE
    Donlon, Kate C.
    McElroy, Thomas
    Jensen, John B.
    HERPETOLOGICAL CONSERVATION AND BIOLOGY, 2021, 16 (03) : 542 - 552
  • [28] Genetic diversity and population structure of Ottelia alismoides (Hydrocharitaceae), a vulnerable plant in agro-ecosystems of Japan
    Wagutu, Godfrey Kinyori
    Tengwer, Miriam Chepkwemoi
    Jiang, Wei
    Li, Wei
    Fukuoka, Goo
    Wang, Guangxi
    Chen, Yuanyuan
    GLOBAL ECOLOGY AND CONSERVATION, 2021, 28
  • [29] Population genetic structure and adaptation of malaria parasites on the edge of endemic distribution
    Duffy, Craig W.
    Ba, Hampate
    Assefa, Samuel
    Ahouidi, Ambroise D.
    Deh, Yacine B.
    Tandia, Abderahmane
    Kirsebom, Freja C. M.
    Kwiatkowski, Dominic P.
    Conway, David J.
    MOLECULAR ECOLOGY, 2017, 26 (11) : 2880 - 2894
  • [30] Range-wide population genetic structure of Symbiodinium associated with the Caribbean Sea fan coral, Gorgonia ventalina
    Andras, Jason P.
    Kirk, Nathan L.
    Harvell, C. Drew
    MOLECULAR ECOLOGY, 2011, 20 (12) : 2525 - 2542