Assessment of Genetic Diversity of the Salangid, Neosalanx taihuensis, Based on the Mitochondrial COI Gene in Different Chinese River Basins

Simple Summary In the current study, we estimate the genetic diversity of the salangid Neosalanx taihuensis sampled from 11 populations in the six typical river basins of China. Using the COI gene sequencing technology, the N. taihuensis population’s genetic difference within and between river basins was investigated. Significant levels of genetic subdivision were detected among populations within basins rather than between basins. Population history dynamics showed that N. taihuensis populations experienced a population expansion during the glacial period in the late Pleistocene. These results suggest that different populations should be considered as different management units to achieve effective conservation and management purposes. Abstract The salangid Neosalanx taihuensis (Salangidae) is a commercially important economical fish endemic to China and restricted to large freshwater systems with a wide-ranging distribution. This fish species has continuous distribution ranges and a long-introduced aquaculture history in Chinese basins. However, the research on its population genetic differentiation within and between basins is very limited. In this regard, 197 individuals were sampled from 11 populations in the Nenjiang River Basin (A1–A4), Songhua River Basin (B1), Yellow River Basin (C1–C2), Yangtze River Basin (D1), Lanchang River Basin (E1–E2) and Huaihe River Basin (F1). Based on the COI sequence, the N. taihuensis population’s genetic difference within and between river basins was investigated. The haplotypes and their frequency distributions were strongly skewed, with most haplotypes (n = 13) represented only in single samples each and thus restricted to a single population. The most common haplotype (H4, 67/197) was found in all individuals. The analysis of molecular variance (AMOVA) revealed a random pattern in the distribution of genetic diversity, which is inconsistent with contemporary hydrological structure. The mismatch between the distribution and neutrality tests supported the evidence of a population expansion, which occurred during the late Pleistocene (0.041–0.051 million years ago). Significant levels of genetic subdivision were detected among populations within basins rather than between the six basins. Population history dynamics showed that N. taihuensis experienced an expansion during the glacial period in the late Pleistocene. Therefore, different populations should be considered as different management units to achieve effective conservation and management purposes. These results have great significance for the evaluation and exploitation of the germplasm resources of N. taihuensis.

[1]  Shenmin Zhang,et al.  China's biodiversity conservation in the process of implementing the sustainable development goals (SDGs) , 2022, Journal of Cleaner Production.

[2]  A. Carosi,et al.  Phylogeography and population structure of Squalius lucumonis: a baseline for conservation of an Italian endangered freshwater fish , 2021, Journal for Nature Conservation.

[3]  Yifeng Chen,et al.  Understanding patterns of taxonomic diversity, functional diversity, and ecological drivers of fish fauna in the Mekong River , 2021, Global Ecology and Conservation.

[4]  Yan Wang,et al.  Threats and protection policies of the aquatic biodiversity in the Yangtze River , 2020 .

[5]  Rosalee S. Hellberg,et al.  Development of a DNA mini-barcoding protocol targeting COI for the identification of elasmobranch species in shark cartilage pills , 2020 .

[6]  B. K. Hand,et al.  Aquatic Landscape Genomics and Environmental Effects on Genetic Variation. , 2019, Trends in ecology & evolution.

[7]  Wenxi Lu,et al.  Land Use Change Impacts on Hydrology in the Nenjiang River Basin, Northeast China , 2019, Forests.

[8]  Jin-Xian Liu,et al.  Comprehensive assessment of population genetic structure of the overexploited Japanese grenadier anchovy (Coilia nasus): Implications for fisheries management and conservation , 2019, Fisheries Research.

[9]  S. Ouyang,et al.  Biodiversity decline of fish assemblages after the impoundment of the Three Gorges Dam in the Yangtze River Basin, China , 2019, Reviews in Fish Biology and Fisheries.

[10]  J. Ni,et al.  Geocode-based Aquatic Habitats in Hierarchical System of the Yellow River Basin , 2018 .

[11]  Xiaofei Liu,et al.  The development of biodiversity conservation measures in China's hydro projects: A review. , 2017, Environment international.

[12]  M. Miya,et al.  Structure and variation of the mitochondrial genome of fishes , 2016, BMC Genomics.

[13]  Wei Chen,et al.  Genetic variation and population history of three Carassius auratus populations in Huaihe River, China , 2016, Mitochondrial DNA. Part A, DNA mapping, sequencing, and analysis.

[14]  Fei Xiong,et al.  Isolation and characterization of 19 polymorphic microsatellite loci from Neosalanx taihuensis, a rapidly invasive and adaptative species , 2015 .

[15]  J. Dupont,et al.  Fungal endophytes of Vanilla planifolia across Réunion Island: isolation, distribution and biotransformation , 2015, BMC Plant Biology.

[16]  Yushun Chen,et al.  Using whole body elemental fingerprint analysis to distinguish different populations of Coilia nasus in a large river basin , 2015 .

[17]  F. Bardakci,et al.  Investigation of Chironomidae (Diptera) relationships using mitochondrial COI gene , 2015 .

[18]  Jianfeng Tang,et al.  Growth and reproduction of the non‐native icefish Neosalanx taihuensis Chen, 1956 (Salangidae) in a plateau lake, southwestern China , 2014 .

[19]  T. Hodkinson,et al.  High levels of gene flow and genetic diversity in Irish populations of Salix caprea L. inferred from chloroplast and nuclear SSR markers , 2014, BMC Plant Biology.

[20]  C. Xie,et al.  Assessing the genetic diversity and population structure of Culter alburnus in China based on mitochondrial 16S rRNA and COI gene sequences , 2013 .

[21]  S. Xie,et al.  Variation in early growth of Neosalanx taihuensis between two populations above and below the Three Gorges Dam, China , 2013 .

[22]  T. Patarnello,et al.  Restricted gene flow at the micro- and macro-geographical scale in marble trout based on mtDNA and microsatellite polymorphism , 2011, Frontiers in Zoology.

[23]  P. Trontelj,et al.  Lack of genetic structure in the jellyfish Pelagia noctiluca (Cnidaria: Scyphozoa: Semaeostomeae) across European seas. , 2010, Molecular phylogenetics and evolution.

[24]  L. Excoffier,et al.  Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows , 2010, Molecular ecology resources.

[25]  P. Czerniejewski Changes in condition and in carapace length and width of the Chinese mitten crab (Eriocheir sinensis H. Milne Edwards, 1853) harvested in the Odra River estuary in 1999-2007 , 2010 .

[26]  B. Murphy,et al.  Two spawning stocks of icefish Neosalanx taihuensis revealed from annual reproductive cycle analyses , 2009, Fisheries Science.

[27]  Pablo Librado,et al.  DnaSP v5: a software for comprehensive analysis of DNA polymorphism data , 2009, Bioinform..

[28]  Liang Zhao,et al.  Complex population genetic and demographic history of the Salangid, Neosalanx taihuensis, based on cytochrome b sequences , 2008, BMC Evolutionary Biology.

[29]  D. Byers Evolution in heterogeneous environments and the potential of maintenance of genetic variation in traits of adaptive significance , 2005, Genetica.

[30]  Laurent Excoffier,et al.  Arlequin (version 3.0): An integrated software package for population genetics data analysis , 2005, Evolutionary bioinformatics online.

[31]  G. Lei,et al.  Freshwater fish biodiversity in the Yangtze River basin of China: patterns, threats and conservation , 2003, Biodiversity & Conservation.

[32]  Kurt Lambeck,et al.  Links between climate and sea levels for the past three million years , 2002, Nature.

[33]  Zhengwen Liu The introduction of icefish, Neosalanx taihuensis Chen, in China with special reference to the subtropical lakes of the Yunnan Plateau (southwest China) , 2001 .

[34]  L. Excoffier,et al.  Estimation of past demographic parameters from the distribution of pairwise differences when the mutation rates vary among sites: application to human mitochondrial DNA. , 1999, Genetics.

[35]  B. Bowen,et al.  Shallow population histories in deep evolutionary lineages of marine fishes: insights from sardines and anchovies and lessons for conservation , 1998 .

[36]  J. Thompson,et al.  The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. , 1997, Nucleic acids research.

[37]  Y. Fu,et al.  Statistical tests of neutrality of mutations against population growth, hitchhiking and background selection. , 1997, Genetics.

[38]  W. Li,et al.  Statistical tests of neutrality of mutations. , 1993, Genetics.

[39]  H. Harpending,et al.  Population growth makes waves in the distribution of pairwise genetic differences. , 1992, Molecular biology and evolution.

[40]  Gerald R. Smith Introgression in fishes : significance for paleontology, cladistics, and evolutionary rates , 1992 .

[41]  F. Tajima Statistical method for testing the neutral mutation hypothesis by DNA polymorphism. , 1989, Genetics.

[42]  N. Blin,et al.  A general method for isolation of high molecular weight DNA from eukaryotes. , 1976, Nucleic acids research.

[43]  L. Hongyan,et al.  Population genetic structure of Neosalanx taihuensis between invasive and original areas revealed by microsatellite DNA , 2016 .

[44]  Ghram Abdeljelil,et al.  Genetic diversity and population structure of Sepia officinalis from the Tunisian cost revealed by mitochondrial COI sequences , 2014, Molecular Biology Reports.

[45]  O. Othman Mitochondrial DNA as a Marker for Genetic Diversity and Evolution , 2012 .

[46]  L. Guangchun,et al.  Genetic diversity of Neosalanx taihuensis based on mitochondrial COI sequences , 2012 .

[47]  E. Baran,et al.  Fish biodiversity research in the Mekong Basin , 2012 .

[48]  H. Bandelt,et al.  Median-joining networks for inferring intraspecific phylogenies. , 1999, Molecular biology and evolution.

[49]  P. Xie,et al.  Threats to biodiversity in Chinese inland waters , 1999 .