Journals / Turkish Journal of Zoology / 2020 / Cilt: 44 - Sayı: 1

Genetic structure and population dynamics of the silver pheasant (Lophura nycthemera) in southern China

Pages
31–43
Publication Date
2022-11-05
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

The weak phylogeographic and complex historical expansion population of the silver pheasant during the interglacial periodcould probably be related to its complex topography and the sufficient amount of suitable habitats and food resources in southern China.

📌 3 Key Takeaways

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Objective & Hypothesis:In southern China, the silver pheasant (Lophura nycthemera) is a widespread species due to complex topography and sufficienthabitats and food resources.
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Key Findings & Data:We investigated the microsatellite and mitochondrial DNA control region sequence of 115 individuals from7 locations in China to study population dynamics of the silver pheasant during the Pleistocene.
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Conclusion & Impact:The weak phylogeographic and complex historical expansion population of the silver pheasant during the interglacial periodcould probably be related to its complex topography and the sufficient amount of suitable habitats and food resources in southern China.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

In southern China, the silver pheasant (Lophura nycthemera) is a widespread species due to complex topography and sufficienthabitats and food resources. We investigated the microsatellite and mitochondrial DNA control region sequence of 115 individuals from7 locations in China to study population dynamics of the silver pheasant during the Pleistocene. The neutrality test and mismatchdistribution analyses showed that population expansion began in the interglacial period (76,053 years ago), and the latest commonancestor appeared approximately 970,300 years ago. Most populations exhibited a high level of genetic diversity as well as gene flow.Results of phylogenetic trees and network and STRUCTURE analyses provided insights into the weak population structure of thisspecies. The weak phylogeographic and complex historical expansion population of the silver pheasant during the interglacial periodcould probably be related to its complex topography and the sufficient amount of suitable habitats and food resources in southern China.

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Cite This Article

CHEN, P., LU, W., YU, L., XU, Z., RUAN, L., BAI, J., HAN, Y., ZHU, C., SUN, G., ZHAO, D., ZHANG, Z., CHENG, J. (2022). Genetic structure and population dynamics of the silver pheasant (Lophura nycthemera) in southern China. Turkish Journal of Zoology, Cilt: 44 - Sayı: 1, 31–43. https://ajindex.com/articles/615967

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References (5)

  1. Alain H, Randi E, Lucchini V (1998). Genetic diversity, phylogenetic relationships and conservation of Edwards’s Pheasant Lophura edwardsi. Bird Conservation International 8 (4): 395-410. doi: 10.1017/s095927090000215x Alasaad S, Soriguer RC, Chelomina G, Sushitsky YP, Fickel J (2011). Siberian tiger’s recent population bottleneck in the Russian Far East revealed by microsatellite markers. Mammalian Biology 76 (6): 722-726.
  2. Aleixo A (2004). Historical diversification of a Terra-firme forest bird superspecies: a phylogeographic perspective on the role of different hypotheses of Amazonian diversification. Evolution 58 (6): 1303-1317. doi: 10.2307/3449226 Anthony NM, Johnson-Bawe M, Jeffery K, Clifford SL, Abernethy KA et al. (2007). The role of Pleistocene refugia and rivers in shaping gorilla genetic diversity in central Africa. Proceedings of the National Academy of Sciences of the United States of America 104 (51): 20432-20436.
  3. Bandelt HJ, Forster P, Röhl A (1999). Median-joining networks for inferring intraspecific phylogenies. Molecular Biology and Evolution 16 (1): 37-48. doi: 10.1093/oxfordjournals.molbev. a026036 Beerli P, Palczewski M (2010). Unified framework to evaluate panmixia and migration direction among multiple sampling locations. Genetics 185 (1): 313-326.
  4. Brown JA, Swank RT (1983). Subcellular redistribution of newly synthesized macrophage lysosomal enzymes. Correlation between delivery to the lysosomes and maturation. Journal of Biological Chemistry 258 (24): 15323-15328. doi: 10.1016/ S0015-7368(92)73045-X Cao F, Qi C, Li G, Zhong C, Tang D et al. (2012). Climate change effects on southern subtropical and tropical tree species in Ganzhou City, China. British Journal of Environment and Climate Change 2 (2): 163-179. doi: 10.9734/BJECC/2012/1114 Clement M, Crandall KPD (2000). TCS: A computer program to estimate gene genealogies. Molecular Ecology 9 (10): 1657- 1659. doi: 10.1046/j.1365-294x.2000.01020.x Clinton LK, Billings LM, Green KN, Caccamo A, Ngo J et al. (2007). Age-dependent sexual dimorphism in cognition and stress response in the 3xTg-AD mice. Neurobiology of Disease 28 (1): 76-82. doi: 10.1016/j.nbd.2007.06.013 Cornuet JM, Luikart G (1996). Description and power analysis of two tests for detecting recent population bottlenecks from allele frequency data. Genetics 144 (4): 2001-2014.
  5. Cornuet JM, Piry S, Luikart G, Estoup A, Solignac M (1999). New methods employing multilocus genotypes to select or exclude populations as origins