Skip to main content

Advertisement

Log in

AFLP and ISSR analysis reveals high genetic variation and inter-population differentiation in fragmented populations of the endangered Litsea szemaois (Lauraceae) from Southwest China

  • Original Article
  • Published:
Plant Systematics and Evolution Aims and scope Submit manuscript

Abstract

Litsea szemaois (Lauraceae) is an endemic and endangered species from the tropical rain forests of Xishuangbanna, southern Yunnan, SW China, but habitat fragmentation, especially exacerbated by rubber planting, has caused a decline in population size of the species. AFLP and ISSR were used to investigate the genetic diversity and population structure of eight populations from across its known distribution. Three AFLP and ten ISSR primer combinations produced a total of 203 and 77 unambiguous and repeatable bands respectively, of which 164 (80.8%) and 67 (87.0%) were polymorphic for the two markers. These two markers showed that Litsea szemaois exhibits comparatively high genetic diversity at species level (heterozygosity (hs) = 0.2109) relative to some other Lauraceae. Most of the genetic variation was partitioned within populations, but genetic differentiation between populations was significant and relatively high (Φ st = 0.2420, θ= 0.1986) compared with other tropical plants. The genetic characteristics of L. szemaois may be related to its outbreeding system, insect pollination and fragmented distribution. Because L. szemaois is dioecious and slow to mature, ex situ conservation across its genetic diversity is unlikely to succeed, although seedlings grow well under cultivation. Thus, in situ conservation is very important for this endangered species, especially as only 133 adult individuals are known in the wild. In particular, the Nabanhe and Mandian populations should be given a high conservation priority due to their higher genetic diversity, larger population size and better field condition, but wider sampling is required across all populations to determine additional areas with significant genetic conservation value.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  • Allen CK (1938) Studies in the Lauraceae. I. Chinese and Indo-Chinese species of Litsea, Neolitsea and Actinodaphne. Ann Missouri Bot Gard 25:361–434

    Article  Google Scholar 

  • Barrett SCH, Kohn JS (1991) Genetic and evolutionary consequences of small population size in plants: implications for conservation. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, pp 3–30

    Google Scholar 

  • Bensch S, Åkesson M (2005). Ten years of AFLP in ecology and evolution: why so few animals? Molec Ecol 14:2899–2914

    Article  CAS  Google Scholar 

  • Bussell JD (1999) The distribution of random amplified polymorphic DNA (RAPD) diversity amongst populations of Isotoma petraea (Lobelaceae). Molec Ecol 8:775–789

    Article  CAS  Google Scholar 

  • Cardoso MA, Provan J, Powell W, Ferreira PCG, Oliveira DE (1998) High genetic differentiation among remnant populations of the endangered Caesalpinia echinata Lam. (Leguminosae-Caesalpinioideae). Molec Ecol 7:601–608

    Article  Google Scholar 

  • Chung MG, Chung MY, Son OHG, Epperson BK (2000) Spatial genetic struture in a Neolitsea sericea population (Lauraceae). Heredity 85:490–497

    Article  PubMed  Google Scholar 

  • Chung MY, Nason JD, Epperson BK, Chung MG (2003) Temporal aspects of the fine-scale genetic structure in a population of Cinnamomum insularimontanum (Lauraceae). Heredity 90:98–108

    Article  PubMed  CAS  Google Scholar 

  • Devy MS, Davidar P (2003) Pollination systems of trees in Kakachi, a mid-elevation wet evergreen forest in Western Ghats, India. Amer J Bot 90:650–657

    Article  Google Scholar 

  • Doyle JJ, Doyle JL (1987) A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull 19:11–15

    Google Scholar 

  • Ellis JR, Pashiey CH, Burke JM, Mccauley DE (2006) High genetic diversity in a rare and endangered sunflower as compared to a common congener. Molec Ecol 15:2345–2355

    Article  CAS  Google Scholar 

  • Excoffier L, Smouse PE, Quattro JM (1992) Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131:479–491

    PubMed  CAS  Google Scholar 

  • Falk DA, Holsinger KE (1991) Genetics and conservation of rare plants. Oxford University Press, New York

    Google Scholar 

  • Fan Y-B, Wang R-M, Pan F-J, Yang P-S (2006) Study of the floral and pollination biology of Cinamomum camphora and Litsea cubeba (Lauraceae). J Taiwan Mus 59:75–90

    Google Scholar 

  • Frankham R, Ballou JD, Briscoe DA (2002) Introduction to conservation genetics. Cambridge University Press, Cambridge

    Google Scholar 

  • Glover BJ, Abbott RJ (1995) Low genetic diversity in the Scottish endemic Primula scotica Hook. New Phytol 129:147–153

    Article  Google Scholar 

  • Hamrick JL (1990) Isozymes and the analysis of genetic structure in plant populations. In: Soltis ED, Soltis PS (eds) Isozymes in plant biology. Chapman and Hall, London, pp 87–105

    Google Scholar 

  • Hamrick JL, Godt MJW (1989) Allozyme diversity in plant species. In: Brown ADH, Clegg MT, Kahler AL, Weir BS (eds) Plant population genetics, breeding and genetic resources. Sinauer, Sunderland, pp 43–63

    Google Scholar 

  • Hamrick JL, Godt MJW (1996) Effects of life history traits on genetic diversity in plant species. Philos Trans Roy Soc Lond B 351:1291–1298

    Article  Google Scholar 

  • Hamrick JL, Loveless MD (1989) The genetic structure of tropical tree populations: Associations with reproductive biology. In: Bock JH, Linhart YB (eds) Plant evolutionary ecology. Westview Press, Boulder Colo, pp 131–146

    Google Scholar 

  • Hamrick JL, Godt MJW, Murawski DA, Loveless MD (1991) Correlations between species traits and allozyme diversity: implications for conservation biology. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, p 5–86

    Google Scholar 

  • Hogbin PM, Peakall R (1999) Evaluation of the contribution of genetic research to the management of the endangered plant Zieria prostrata. Conserv Biol 13:514–522

    Article  Google Scholar 

  • Holsinger KE (1999) Analysis of genetic diversity in geographically structured population: a Bayesian perspective. Hereditas 130:245–255

    Article  Google Scholar 

  • Holsinger KE, Gottlieb LD (1991) Conservation of rare and endangered plants: principles and prospects. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, pp 195–208

    Google Scholar 

  • Holsinger KE, Lewis PO (2006) HICKORY version 1.0.4. Department of Ecology and Evolutionary Biology, University of Connecticut, USA (Program available from http://darwin.eeb.uconn.edu/hickory/software.html)

  • Holsinger KE, Wallace LE (2004) Bayesian approaches for the analysis of population genetic structure: an example from Platanthera leucophaea (Orchidaceae). Molec Ecol 13:887–897

    Article  Google Scholar 

  • Holsinger KE, Lewis PO, Dey DK (2002) A Bayesian approach to inferring population structure from dominant markers. Molec Ecol 11:1157–1164

    Article  CAS  Google Scholar 

  • Jones CJ, Dwards KJ, Castaglione S, Sala F, van de Wiel C, Bredemeijer G, Vosman B, Matthes M, Daly A, Brettschneider R, Bettini P, Buiatti M, Maestri E, Malcevschi A, Marmiroli N, Aert R, Volckaert G, Rueda J, Linacero R, Vazquez A, Karp A (1997) Reproducibility testing of RAPD, AFLP and SSR markers in plants by a network of European laboratories. Molec Breed 3:381–390

    Article  CAS  Google Scholar 

  • Kam TL, Rob M, Tien YC, Edward T (2004) A comparison of AFLP and ERIC-PCR analyses for discriminating Escherichia coli from cattle, pig and human sources. FEMS Microbiol Ecol 47:111–119

    Article  CAS  Google Scholar 

  • Kang M, Ye Q-G, Huang H-W (2005) Genetic consequence of restricted habitat and population decline in endangered Isoetes sinensis (Isoetaceae). Ann Bot 96:1265–1274

    Article  PubMed  CAS  Google Scholar 

  • Karron JD (1991) Patterns of genetic variation and breeding system in rare plant species. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, pp 87–98

    Google Scholar 

  • Li J-M, Jin Z-X (2006) High genetic differentiation revealed by RAPD analysis of narrowly endemic Sinocalycanthus chinensis Cheng et S.Y. Chang, an endangered species of China. Biochem Syst Ecol 34:725–735

    Article  CAS  Google Scholar 

  • Li J, Li H-W (2006) Notes on the plants of genus Litsea (Lauraceae) from China. Act Bot Yun 28:103–107

    Google Scholar 

  • Li H-W, Pai P-Y, Lee S-K, Wei F-N, Wei Y-T, Yang Y-C, Huang P-H, Tsui H-P, Shia Z-D, Li J-L (1984) Lauraceae. In: Li H-W (eds) Flora reipublicae popularis sinicae, vol 31. Science Press, Beijing, pp 1–463

    Google Scholar 

  • Li J, Christophel DC, Conran JG, Li H-W (2004) Phylogenetic relationships within the Litsea complex (Lauraceae) inferred from sequences of the chloroplast gene matK and nuclear ribosomal DNA ITS regions. Pl Syst Evol 246:19–34

    Article  CAS  Google Scholar 

  • Li H-M, Aide TM, Ma Y-X, Liu W-J, Cao M (2007) Demand for rubber is causing the loss of high diversity rain forest in SW China. Biodivers Conserv 16:1731–1745

    Article  Google Scholar 

  • Liou H (1934) Lauracées de Chine et D’Indochine. Hermann & Gie, Éditeurs, Paris

    Google Scholar 

  • Liu W-J, Ma Y-X, Hu H-B, Cao M, Wang W (2005) Land use and land cover change in the tropical rainforest region of southern Yunnan - a case study of Menglun, Xishuangbanna. J Mt Sci 23:71–79

    Google Scholar 

  • Loveless MD (1992) Isozyme variation in tropical trees: patterns of genetic organization. New For 6:67–94

    Google Scholar 

  • Loveless MD, Hamrick JL (1984) Ecological determinants of genetic structure in plant populations. Annual Rev Ecol Syst 15:65–95

    Article  Google Scholar 

  • Masayuki M (2003) Population genetics of threatened wild plants in Japan. J Pl Res 116:169–174

    Google Scholar 

  • Miller MP (1997) Tools for population genetic analysis (TFPGA), version 1.3: a Windows program for the analysis of allozyme and molecular population genetic data. Department of Biological Sciences Northern Arizona University, USA (Program available from: http://www.marksgeneticsoftware.net/tfpga.htm)

  • Moyle LC (2006) Correlates of genetic differentiation and isolation by distance in 17 congeneric Silene species. Molec Ecol 15:1067–1081

    Article  CAS  Google Scholar 

  • Myers N, Mittermeier RA, Mittermeier CG, da Fonseca GAB, Kent J (2000) Biodiversity hotspots and conservation priorities. Nature 403:853–858

    Article  PubMed  CAS  Google Scholar 

  • Neigel JE (1996) Estimation of effective population size and migration parameters from genetic data. In: Smith TB, Wayne RK (eds) Molecular genetic approaches in conservation. Oxford University Press, New York, pp 329–346

    Google Scholar 

  • Nybom H (2004) Comparison of different nuclear DNA markers for estimating intraspecific genetic diversity in plants. Molec Ecol 13:1143–1155

    Article  CAS  Google Scholar 

  • Ranker TA (1994) Evolution of high genetic variability in the rare Hawaiian fern Adenophorus periens and implications for conservation management. Biol Conserv 70:19–24

    Article  Google Scholar 

  • Rohwer JG (1993) Lauraceae. In: Kubitzki K, Rohwer JG, Bittrich V (eds) The families and genera of vascular plants, vol 2. Springer-Verlag, Berlin, pp 366–391

    Google Scholar 

  • Rolf JF (2000) NTSYS-pc. Numerical taxonomy and multi-variate analysis system, version 2.1. Exeter Software, Setauket

    Google Scholar 

  • Rousset F (1997) Genetic differentiation and estimation of gene flow from F-Statistics under Isolation by distance. Genetics 145:1219–1228

    PubMed  CAS  Google Scholar 

  • Schaal BA, Leverich WJ, Rogstad SH (1991) Comparison of methods for assessing genetic variation in plant conservation biology. In: Falk DA, Holsinger KE (eds) Genetics and conservation of rare plants. Oxford University Press, New York, pp 123–134

    Google Scholar 

  • Schmidt K, Jensen K (2000) Genetic structure and AFLP variation of remnant populations in the rare plant Pedicularis palustris (Scrophulariacae) and its relation to population size and reproductive components. Amer J Bot 87:678–689

    Article  CAS  Google Scholar 

  • SPSS (2005) Statistical software package, Version 13.0. SPSS Inc, Chicago

    Google Scholar 

  • Suyama Y, Obayashi K, Hayashi I (2000) Clonal structure in a dwarf bamboo (Sasa senanensis) population inferred from amplified fragment length polymorphism (AFLP) fingerprints. Molec Ecol 9:901–906

    Article  CAS  Google Scholar 

  • Tero N, Aspi J, Siikamäki P, Jäkäläniemi A, Tuomi J (2003) Genetic structure and gene flow in a metapopulation of an endangered plant species, Silene tatarica. Molec Ecol 12:2073–2085

    Article  CAS  Google Scholar 

  • Vos P, Hogers R, Bleeker M, Reijand M, van de Lee T, Hornes M, Frijers A, Pot J, Peleman J, Kuiper M, Zabeau M (1995) AFLP: a new technique for DNA fingerprinting. Nucleic Acids Res 23:4407–4414

    Article  PubMed  CAS  Google Scholar 

  • Wang S, Xie Y (eds) (2003) China species red list. High Education Press, Beijing, pp 330–334

  • Wang Z-F, Gao S-H, Tian S-N, Fu S-L, Ren H, Peng S-L (2005a) Genetic structure of Cryptocarya chinensis in fragmented lower subtropical forests in China based on ISSR markers. Biodivers Sci 13:324–331

    Article  CAS  Google Scholar 

  • Wang Z-S, An S-Q, Liu H, Leng X, Zheng J-W, Liu Y-H (2005b) Genetic structure of the endangered plant Neolitsea sericea (Lauraceae) from the Zhoushan Archipelago using RAPD markers. Ann Bot 95:305–313

    Article  PubMed  CAS  Google Scholar 

  • Wright S (1978) Evolution and the genetics of populations, variability within and among natural populations, vol 4. University of Chicago Press, Chicago

    Google Scholar 

  • Zabeau M, Vos P (1993) European Patent Application Number: 92402629 7 (Publication Number: 0534858 A)

  • Zhang F-M (2002) DCFA 1.1, a program companied with AMOVA to compute the matrix of distance. Laboratory of Systematics and Evolutionary Botany, Institute of Botany, the Chinese Academy of Sciences, Beijing

    Google Scholar 

  • Zietkiewicz E, Rafalski A, Labuda D (1994) Genome fingerprinting by simple sequence repeats (SSR)-anchored PCR amplification. Genomics 20:176–183

    Article  PubMed  CAS  Google Scholar 

  • Zhu H (2004) A tropical seasonal rain forest at its altitudinal and latitudinal limits in southern Yunnan, SW China. Gard Bull Singap 56:55–72

    Google Scholar 

Download references

Acknowledgments

Guo-Da Tao and Hsi-Wen Li are thanked for their assistance with field collection, and we are indebted to Fu-Min Zhang for access to the software DCFA 1.1. We are also grateful to Song Ge, Yun-Qian Hu, Long-Qian Xiao, Hong-Mei Li, Shu-Li Wang and Zhi-Ming Li for their helpful suggestions, and Barbara Rudolph and Kristina Groth from University of Hamburg for comments and changes to an earlier manuscript. John Conran from The University of Adelaide is thanked for assistance with the current manuscript. The project “Conservation Genetics of Litsea szemaois” from the program “the Light of Western China” of CAS, and The National Natural Science Foundation of China (grant number 30470123) jointly funded this work.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jie Li.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ci, Xq., Chen, Jq., Li, Qm. et al. AFLP and ISSR analysis reveals high genetic variation and inter-population differentiation in fragmented populations of the endangered Litsea szemaois (Lauraceae) from Southwest China. Plant Syst Evol 273, 237–246 (2008). https://doi.org/10.1007/s00606-008-0012-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00606-008-0012-4

Keywords

Navigation